SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs4187 | in-del | -/ATAAAG/TAAAGA | 0.499308 | 0.0185838 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49532197 | TGTATTTAAAAAAAA[-/ATAAAG/TAAAGA]TAATCAAATGCTTTT | 55213 |
rs16659 | in-del | -/ACTTTATCATCTTTC | 0 | 0 | utr-variant-3-prime, cds-indel, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533076 | ATTGGCTTATGTGAA[-/ACTTTATCATCTTTC]ACTTTTGGTTTTCCT | 55213 |
rs729051 | snp | A/G | 0.00795532 | 0.062565 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546073 | CAACCTGGATCACTG[A/G]TGGGTAAAAGAATAC | 55213 |
rs874398 | snp | C/T | 0.431473 | 0.171952 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551155 | CTCCTTCTCCCTCCC[C/T]GCTTCCCCCTTCCCC | 55213 |
rs882970 | snp | A/C | 0.444799 | 0.156695 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49570859 | GACAGATGAGGACTG[A/C]GGCTCAAAGGTGAAA | 55213 |
rs942871 | snp | A/G | 0.498693 | 0.0255257 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49550485 | GGACATAGGAGGTAA[A/G]ACCTTACAATTAGGC | 55213 |
rs1046027 | snp | A/G | 0.487558 | 0.0778863 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533187 | CTACTATATATGACT[A/G]GAAGAAGTGGTTCTT | 55213 |
rs1046028 | snp | A/G | 0.487368 | 0.0784625 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533153 | GTCAACCCTCTTACA[A/G]GACTTAGTGGAATTT | 55213 |
rs1046034 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49532675 | AATTTGTGTCTATTG[G/T]GGTGGGAAGGGGAGT | 55213 |
rs1062975 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533780 | GGAAGTTGGCAGCAC[A/T]CTCCTGGGCCATGTA | 55213 |
rs1062979 | snp | C/G | 0.487113 | 0.0792303 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533239 | CATGTATAGTATACT[C/G]TTGCCTTCCTAAATT | 55213 |
rs1128767 | snp | G/T | 0.487432 | 0.0782705 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533095 | CACACATTGGCTTAT[G/T]TGAAACTTTATCATC | 55213 |
rs1198421 | snp | C/T | 0.162909 | 0.23434 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49575719 | taaagacaggaacaa[C/T]agacactggagacta | 55213 |
rs1198422 | snp | A/G | 0.165853 | 0.235413 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581606 | ggaaaaaagcaagtg[A/G]aataaggagagcaga | 55213 |
rs1325658 | snp | G/T | 0.311614 | 0.242289 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586896 | TTTTCTTCAACAGCC[G/T]CCAAAGTACACATCA | 55213 |
rs1325659 | snp | A/G | 0.444267 | 0.157354 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586906 | CAGCCTCCAAAGTAC[A/G]CATCAGTTTCCTACT | 55213 |
rs1359541 | snp | A/G | 0.47709 | 0.104548 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49584803 | TACATGCAAATAAAT[A/G]AAAACAAAAGGCCAC | 55213 |
rs1359542 | snp | A/G | 0.261608 | 0.24973 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49584937 | GCACGCCTGGATAAA[A/G]GTCCTCACTAACAAA | 55213 |
rs1359543 | snp | A/G | 0.477004 | 0.104734 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49585029 | GCACTACTCTCAGGA[A/G]ACGAAGGAGAGATGC | 55213 |
rs1409013 | snp | A/T | 0.146314 | 0.227484 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49543254 | GGGTGACAGAATGAG[A/T]CTCTGTCTCAAAAAA | 55213 |
rs1536192 | snp | A/G | 0.2462 | 0.249971 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546849 | CACCTCCTGCCGTGC[A/G]ACCCAGTTAATAACA | 55213 |
rs1536195 | snp | C/T | 0.279991 | 0.248195 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541533 | AACTACACAATACTA[C/T]TTTTAAAGATACTTA | 55213 |
rs1570883 | snp | A/G | 0.279991 | 0.248195 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49547075 | TACAAATCTGAAGAT[A/G]TGTACAGAAGTGCTT | 55213 |
rs1570884 | snp | A/G | 0.498673 | 0.0257246 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49547375 | GAAAATTAACCTTCA[A/G]TATCAATTGCTGAAC | 55213 |
rs1853829 | snp | C/T | 0.495213 | 0.048687 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583691 | AGCTGGGACTACAGG[C/T]GCACACCACCACGCC | 55213 |
rs1886793 | snp | C/T | 0.261332 | 0.249743 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571313 | ATTGCACCACTGCAC[C/T]CCAGCCTGGGGAAGA | 55213 |
rs1925742 | snp | C/T | 0.499998 | 0.000998401 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535448 | AGCTTGACTTTATTA[C/T]AACTTGGTTAGCTGG | 55213 |
rs1925743 | snp | A/G | 0.440746 | 0.161604 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49585117 | AAAACGGCACCCACA[A/G]CAGTCAGACTTCAGC | 55213 |
rs1969881 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542230 | aaaaaaaaaaaaaaG[G/T]AAGTATATTAACTAC | 55213 |
rs1977352 | snp | G/T | 0.499942 | 0.00539106 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535793 | ACTTTGGGAGGCTGA[G/T]GCGGGCAGATCACGA | 55213 |
rs1977353 | snp | A/G | 0.270892 | 0.249126 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542002 | ggtagatcacctgag[A/G]tcaggagttcgagac | 55213 |
rs1998780 | snp | A/G | 0.245061 | 0.249951 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554708 | GCATCTAGGCTGTGC[A/G]CTCCATATGAGAATC | 55213 |
rs1998781 | snp | C/G | 0.245061 | 0.249951 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49555037 | GGGTAACTAAAGGGA[C/G]AGTTGTTAAAAGTAG | 55213 |
rs2002407 | snp | C/T | 0.430136 | 0.173352 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551058 | TGGAGTGCAATGGCA[C/T]GATCTCGGCTCACTG | 55213 |
rs2038881 | snp | A/G | 0.497722 | 0.0336691 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49561041 | ATTCTGATGAAGACA[A/G]CTTTTCTTGTGTTAT | 55213 |
rs2093472 | snp | A/T | 0.499759 | 0.0109798 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571258 | GGCTGAGGCAGGAGA[A/T]TCGCTTGAACCTGGG | 55213 |
rs2104183 | snp | C/T | 0.261884 | 0.249717 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49575809 | tcactacctgggtga[C/T]ggaattattcgtact | 55213 |
rs2274278 | snp | A/G | 0.24909 | 0.249998 | synonymous-codon, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49552246 | TGCCATTGTTTCCCA[A/G]GCCCAGCTGACCGTT | 55213 |
rs2274279 | snp | C/T | 0.429987 | 0.173507 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552354 | AAGAGACAAAAAAAC[C/T]AGCCCATCTAAACAA | 55213 |
rs2274280 | snp | A/G | 0.429987 | 0.173507 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552369 | CAGCCCATCTAAACA[A/G]ATCAGATACTTCCAA | 55213 |
rs2274281 | snp | C/T | 0.442926 | 0.158996 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552531 | TTCCTGTTTAATACA[C/T]GAGGAAGTTGAGCCT | 55213 |
rs2274282 | snp | G/T | 0.429837 | 0.173662 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49555181 | TGTACAGTTGACATT[G/T]TTTCATTGGAAGAGA | 55213 |
rs2274283 | snp | C/T | 0.429087 | 0.174436 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49555463 | TTGTGAAGAAACTGA[C/T]GTGTAATTGAAAAAG | 55213 |
rs2274284 | snp | A/G | 0.263012 | 0.249661 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49555479 | GTGTAATTGAAAAAG[A/G]AGGTAGAAAGGGAAA | 55213 |
rs2296502 | snp | A/T | 0.135838 | 0.222412 | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49540845 | AAAGGGAGTTAAAGG[A/T]GGTCTGGTTTCTGTT | 55213 |
rs2407696 | snp | A/G | 0.5 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538389 | ACATTAGTCAATTAC[A/G]TAACTTGTATTGTAA | 55213 |
rs2407697 | snp | G/T | 0.279991 | 0.248195 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546299 | ACCATGTGACTTTCC[G/T]TCTAACACTCAGATG | 55213 |
rs2897741 | snp | C/T | 0.32627 | 0.238082 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538416 | GTAACCTAAGAAATA[C/T]ACCCTAGAAAGAggc | 55213 |
rs3039280 | in-del | -/A | 0.67801 | 0.108985 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49547175 | GCAAAAAAAAAAAAA[-/A]TACTGTATTATACCT | 55213 |
rs3186012 | snp | C/G | 0.487621 | 0.0776941 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533837 | GTCGTTTTTGGTCTT[C/G]TTTTCATTTTTGATT | 55213 |
rs3186013 | snp | C/T | 0.487432 | 0.0782705 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533768 | AACTCTCCTGGGCCA[C/T]GTATCAACAATCTTC | 55213 |
rs3186024 | snp | C/T | 0.487432 | 0.0782705 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49532448 | GTAACAATCACTGTT[C/T]TATAGGCTTATGATC | 55213 |
rs3215806 | in-del | -/A | 0.430136 | 0.173352 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552346 | TAAGAAGGAAGAGAC[-/A]AAAAAACCAGCCCAT | 55213 |
rs3751381 | snp | C/G | 0.341668 | 0.232587 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49549696 | GTGTGGTGTGCTGTG[C/G]GCTTCTGTGATCATG | 55213 |
rs3751382 | snp | A/C/G/T | 0.35518 | 0.234281 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49549552 | GTGCCGGGGTCAGTC[A/C/G/T]GTGATCCTCCCGCAC | 55213 |
rs3751383 | snp | C/T | 0.34065 | 0.232986 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549513 | CTTCTCCTGCACCGA[C/T]GACGTGTTTGCCTGC | 55213 |
rs3751384 | snp | C/G | 0.485509 | 0.0840565 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549486 | CTGCTTTGCCACTCC[C/G]GCCGTCTCGTGGCGC | 55213 |
rs3764082 | snp | C/G | 0.430136 | 0.173352 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551029 | TGCAACCTTCACTTC[C/G]TGGGTTCAAGTGATT | 55213 |
rs3794376 | snp | A/G | 0.279991 | 0.248195 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49540355 | TGAGTTCTTAATCTG[A/G]GATTCACAGATCTGT | 55213 |
rs3794377 | snp | A/G | 0.499946 | 0.00519141 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49536999 | ATATTAAGACCATCA[A/G]TGCTCTGTGTTTTGT | 55213 |
rs3990354 | in-del | -/CAGA | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535569 | GGTGGGAATGTTAGA[-/CAGA]GTGGAAGGGGCCCAC | 55213 |
rs4085853 | snp | C/T | 0.499831 | 0.00918375 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535979 | AGTGAGCCGAGATCA[C/T]GCCACTGCACTCCAG | 55213 |
rs4941644 | snp | A/G | 0.411578 | 0.190768 | downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49531569 | aactcaggcagtaat[A/G]ctcactcatccgcca | 55213 |
rs4941645 | snp | C/T | 0.28052 | 0.24813 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559457 | gtcaggagatcgaga[C/T]catcctggctaacac | 55213 |
rs4941646 | snp | A/T | 0.444666 | 0.15686 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571662 | GGTTTTGTGGGGCTA[A/T]GTGCCAGGCAGAACA | 55213 |
rs4941647 | snp | C/G | 0.0562535 | 0.1581 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581654 | CTAAGAAACTCCAAC[C/G]GGAAAGGGACAGGGA | 55213 |
rs4941648 | snp | A/G | 0.26326 | 0.249648 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49582029 | atcacagaatgtgat[A/G]gagttgcaggacgtt | 55213 |
rs4942838 | snp | A/T | 0.487432 | 0.0782705 | downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49531771 | attctactatgtctc[A/T]atgaatttgactaag | 55213 |
rs4942839 | snp | G/T | 0.487432 | 0.0782705 | downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49531818 | catcacatagtattt[G/T]tctgtgagtggctta | 55213 |
rs4942840 | snp | C/T | 0.487432 | 0.0782705 | downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49531942 | AAAAAAACAACTCTA[C/T]GTGCCTGTTTTAATG | 55213 |
rs4942841 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49532196 | AGTGTATTTAAAAAA[A/G]ATAATCAAATGCTTT | 55213 |
rs4942842 | snp | A/C | 0.498693 | 0.0255257 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535149 | CACTAATATCTCAGA[A/C]CATCACCCCCACAGA | 55213 |
rs4942843 | snp | A/G | 0.498693 | 0.0255257 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535151 | CTAATATCTCAGAAC[A/G]TCACCCCCACAGAAG | 55213 |
rs4942844 | snp | G/T | 0.0923359 | 0.194016 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542516 | TAAAGTGAAAGAAAT[G/T]CAGAAACAAGAGTTC | 55213 |
rs4942845 | snp | G/T | 0.303938 | 0.244112 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548792 | ggttgctaggggttg[G/T]ggggagaggagaatg | 55213 |
rs4942847 | snp | G/T | 0.0364509 | 0.129988 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559415 | taatcccagcacttt[G/T]ggaggccaaggcggg | 55213 |
rs4942848 | snp | A/G | 0.472875 | 0.113254 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49567209 | GTGCCGAAGACACAC[A/G]CCTTCCGAATAGACG | 55213 |
rs4942849 | snp | A/C | 0.444799 | 0.156695 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571644 | AGACAAGGTTCCCTG[A/C]GAGGTTTTGTGGGGC | 55213 |
rs5803469 | in-del | -/A | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541438 | ACTTAAAAATAAATT[-/A]AAAAAAAAAAAGTCC | 55213 |
rs5803471 | in-del | -/A | 0 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551917 | AAAAAAAAAAAAAAA[-/A]GCATTAGAAAAGCCT | 55213 |
rs5803472 | in-del | -/T | 0.314544 | 0.241524 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551959 | TACTGAATTTTTCCA[-/T]TTTTTTTTTTTTTTT | 55213 |
rs6145049 | in-del | -/TGTG | 0.5 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583387 | GTGTGCTTTTGTGTA[-/TGTG]TGTGTGTGTGTGTGT | 55213 |
rs6420300 | snp | A/C | 0.270621 | 0.249148 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551799 | CAGCTACTCGGGAGG[A/C]TGAGGCAGGAGAATG | 55213 |
rs6561539 | snp | C/G | 0.228547 | 0.249078 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49537993 | ACTTTCGTAGAAAGA[C/G]AAGAAACATTGGAAG | 55213 |
rs6561540 | snp | C/G | 0.245346 | 0.249957 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49543982 | ATGAGCCACCATGCT[C/G]AGCCTAGAACATTCT | 55213 |
rs6561541 | snp | C/T | 0.498693 | 0.0255257 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553144 | CCAAGATCGTGCTAC[C/T]GTACTCCAGCCTGGC | 55213 |
rs6561542 | snp | C/T | 0.270892 | 0.249126 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553384 | TCCCTCGTTAGCAAA[C/T]AGGTGAGCTCTGATG | 55213 |
rs6561544 | snp | G/T | 0.444533 | 0.157025 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49572787 | GAGTGATAAGAGTGA[G/T]ACTCTGTCTCAAAAT | 55213 |
rs7140107 | snp | C/T | 0.429388 | 0.174127 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49561909 | CCAGACTGGCCAACA[C/T]AGTGAAACCCCACAT | 55213 |
rs7317140 | snp | A/T | 0.279726 | 0.248226 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542900 | ATTTTCTTATGTATA[A/T]CACAGTTGTATCTTT | 55213 |
rs7317982 | snp | C/T | 0.499585 | 0.0143996 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49534116 | AGAACCCAGCAGCCT[C/T]GCGCTTCAGTTCTTA | 55213 |
rs7320475 | snp | A/T | 0.432504 | 0.170857 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566304 | aataaataaataaat[A/T]aaAAAGTTGCATTGC | 55213 |
rs7322077 | snp | A/G | 0.495407 | 0.0477027 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534721 | GAAGAGATATGGTCA[A/G]CCTAAAGTGGCACAT | 55213 |
rs7322971 | snp | C/T | 0.381503 | 0.21262 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553583 | GGTTCCAAATAGCCA[C/T]AGGAAAAAGTACTGA | 55213 |
rs7324024 | snp | C/T | 0.258288 | 0.249863 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49587376 | GGCATGGGGTGTGAG[C/T]AATCAAATATGTCCT | 55213 |
rs7325207 | snp | C/G | 0.400147 | 0.19989 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538707 | ggcaacagaacaaga[C/G]cctgtatcaccagga | 55213 |
rs7325667 | snp | A/G | 0.432357 | 0.171014 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566393 | CCACAGCTTTATGGA[A/G]GCAGTCGAAAACCTC | 55213 |
rs7325851 | snp | A/G | 0.493748 | 0.0555599 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539079 | ttcaccatgttggcc[A/G]ggctggtctcaaact | 55213 |
rs7326825 | snp | A/G | 0.498871 | 0.0237351 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539314 | TGGAGTCTTTCTAAA[A/G]GAAGTTTTTATCATG | 55213 |
rs7327411 | snp | C/T | 0.140919 | 0.224948 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539086 | tgttggccaggctgg[C/T]ctcaaactcctgatc | 55213 |
rs7327417 | snp | C/T | 0.494774 | 0.0508504 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539100 | gtctcaaactcctga[C/T]ctcaagtggcccacc | 55213 |
rs7327432 | snp | A/T | 0.419296 | 0.183954 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539122 | tggcccaccttggcc[A/T]cccaaagtgccggga | 55213 |
rs7328126 | snp | A/G | 0.429987 | 0.173507 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554740 | AACTCATGCTTGATG[A/G]TCTGAGGTGGAACAG | 55213 |
rs7328536 | snp | A/G | 0.429987 | 0.173507 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554945 | GCATAGGTAGTAAAT[A/G]GCCTATTTAAGTGGA | 55213 |
rs7328860 | snp | C/T | 0.429987 | 0.173507 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554985 | CAGAGACTAATTTCA[C/T]AGAAATAACCATCAG | 55213 |
rs7329125 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535954 | cttgaacccaggagg[C/T]ggaggttgcagtgag | 55213 |
rs7329797 | snp | A/C | 0.0637235 | 0.166737 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49572410 | CATGACATCTATTAA[A/C]TTTGCCTAAACATGA | 55213 |
rs7332926 | snp | C/G | 0.398174 | 0.201356 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49567762 | CACCAGCACCAACTT[C/G]GATGACAAGGATCAG | 55213 |
rs7333599 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49549089 | gtgagccgagattgc[A/G]ccactgcactccagc | 55213 |
rs7333969 | snp | C/T | 0.49998 | 0.00319482 | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49549181 | tatgaatgttctaaa[C/T]gcaactaaactgtac | 55213 |
rs7334012 | snp | C/T | 0.403509 | 0.197319 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49567761 | CCACCAGCACCAACT[C/T]GGATGACAAGGATCA | 55213 |
rs7336027 | snp | C/T | 0.388964 | 0.20782 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564666 | ggaggctgaggtggg[C/T]ggatcacgaggtcag | 55213 |
rs7336758 | snp | C/G | 0.432357 | 0.171014 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564989 | TAAGGAATAGGATTG[C/G]AGctgtcccgctccc | 55213 |
rs7337571 | snp | G/T | 0.499759 | 0.0109798 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49580417 | TGGCGAGACTCCATT[G/T]CCTTAAAAATAAAAA | 55213 |
rs7337705 | snp | A/G | 0.429837 | 0.173662 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559604 | gagcttgcagtgagc[A/G]gagatcgtgccactg | 55213 |
rs7337971 | snp | A/G | 0.355525 | 0.226637 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559473 | catcctggctaacac[A/G]gtgaaaccctgtctc | 55213 |
rs7338090 | snp | A/G | 0.429688 | 0.173817 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559782 | gtgcatgctggtgac[A/G]gttgtatgacaaggt | 55213 |
rs7339079 | snp | C/T | 0.430583 | 0.172886 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559528 | gggtgtggtggtggg[C/T]gcctgtagtcccagc | 55213 |
rs7981237 | snp | A/G | 0.444 | 0.157683 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569107 | cgggatctgcaccca[A/G]gcaacctgaagcctg | 55213 |
rs7981396 | snp | C/T | 0.444 | 0.157683 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49577790 | TTTAAGTAGCCTAAA[C/T]ATTCTTCAGCATACA | 55213 |
rs7981448 | snp | C/T | 0.381503 | 0.21262 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553002 | TCCTGGCCAACACAG[C/T]GAAACCCCATCTCTA | 55213 |
rs7981952 | snp | C/T | 0.430136 | 0.173352 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553272 | CATTGAAATATTAAT[C/T]TAATTTGTATTTTTG | 55213 |
rs7982423 | snp | C/T | 0.243633 | 0.249919 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569225 | TGTTCTTTTTCTTGT[C/T]CTTGATTTATAAGTA | 55213 |
rs7982445 | snp | C/T | 0.499946 | 0.00519141 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49537486 | TGTCCAATACTCATA[C/T]CCCAGACCAACTTCA | 55213 |
rs7982555 | snp | A/G | 0.499946 | 0.00519141 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49537374 | AATTTATCCCATTAC[A/G]CAAAAAACATTTGTC | 55213 |
rs7982964 | snp | A/G | 0.499946 | 0.00519141 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49537626 | AAATAATACTTCCCA[A/G]CTGTTTCTCTTAACG | 55213 |
rs7983030 | snp | C/T | 0.429987 | 0.173507 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557070 | TGGCTCCAGCACATC[C/T]CAGTCATGAAATCTT | 55213 |
rs7983283 | snp | A/G | 0.316 | 0.241131 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49537775 | GTCTGTACCAAAGGA[A/G]TATCTGGGTGCTCCT | 55213 |
rs7983291 | snp | C/G | 0.499946 | 0.00519141 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49537795 | TGGGTGCTCCTTTGT[C/G]AAGTCCTTCTTAATA | 55213 |
rs7983670 | snp | C/G | 0.430285 | 0.173197 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557254 | TCAACTTAAAAGATA[C/G]GGAATAGAAGGGACT | 55213 |
rs7983672 | snp | C/G | 0.430285 | 0.173197 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557255 | CAACTTAAAAGATAG[C/G]GAATAGAAGGGACTA | 55213 |
rs7985985 | snp | A/G | 0.444533 | 0.157025 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569395 | cctgggcaacatggc[A/G]aaaccccatttctac | 55213 |
rs7986405 | snp | G/T | 0.261332 | 0.249743 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569654 | ccgggaggcagaggt[G/T]gctgtgagccgagac | 55213 |
rs7986417 | snp | C/T | 0.429987 | 0.173507 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553421 | TAAACTAAGGAGTGA[C/T]AGGGGGATCATGAGA | 55213 |
rs7987338 | snp | A/C | 0.432357 | 0.171014 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563153 | acctgtaatcccaac[A/C]ctttgggaggccgag | 55213 |
rs7987806 | snp | A/G | 0.432944 | 0.170387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557434 | ACCTTTAAGATAAGC[A/G]CAACTTGGGGGCTTA | 55213 |
rs7987956 | snp | A/G | 0.432797 | 0.170544 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563218 | cagcctaggcaacat[A/G]gtgagacctcatctc | 55213 |
rs7988350 | snp | A/G | 0.43309 | 0.17023 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557710 | ggatcgcttgagccc[A/G]ggagttcaagaccag | 55213 |
rs7988844 | snp | A/G | 0.426966 | 0.176587 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557729 | gttcaagaccagcct[A/G]ggcaacatagccaga | 55213 |
rs7989286 | snp | G/T | 0.236434 | 0.249632 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557448 | CACAACTTGGGGGCT[G/T]AACAAGTGTTACAGT | 55213 |
rs7989504 | snp | A/G | 0.487495 | 0.0780784 | downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49531646 | atgggtctgtggccc[A/G]agggttggggacccc | 55213 |
rs7989915 | snp | A/G | 0.429987 | 0.173507 | intron-variant, synonymous-codon | RCBTB1 | GRCh38.p7 | 13:49558298 | cacctggtgtcctgc[A/G]ctgccagaagaggct | 55213 |
rs7990896 | snp | C/T | 0.423726 | 0.179776 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548262 | ccaggcatggtggca[C/T]gcgcctgtaatccca | 55213 |
rs7992396 | snp | C/T | 0.270892 | 0.249126 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548367 | gcaccccagcctggg[C/T]aacagagtgagactc | 55213 |
rs7994201 | snp | A/T | 0.477345 | 0.103991 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49585356 | GGAGTAACGGGGCAC[A/T]CCCGGCCCGGCCTGC | 55213 |
rs7994516 | snp | C/T | 0.262435 | 0.249691 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49579517 | TAGTCCCAGCTACTC[C/T]GGAGGCTGAGGCAGG | 55213 |
rs7994612 | snp | A/C | 0.498774 | 0.02473 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49558576 | gcaggcgcctgtaat[A/C]ccagctactcaggag | 55213 |
rs7995006 | snp | C/T | 0.162581 | 0.234218 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539593 | GAGGATTCTAACATC[C/T]GTCACCAAATGGACA | 55213 |
rs7995684 | snp | A/G | 0.487432 | 0.0782705 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49532819 | AAATTCACTAAGGGA[A/G]CTCACTCAAATGGAA | 55213 |
rs7996012 | snp | C/T | 0.262159 | 0.249704 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581503 | TGTGGGATATTAAAG[C/T]GGACAAGTCCCAACA | 55213 |
rs7996134 | snp | C/T | 0.0543475 | 0.155628 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539527 | GTCAGCAAGGTCTGA[C/T]CCTGAGTATGGAACT | 55213 |
rs7996207 | snp | A/G | 0.498832 | 0.0241331 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548545 | gagagtcaaaggtgg[A/G]aacaacccacatgtc | 55213 |
rs7999363 | snp | A/G | 0.499946 | 0.00519141 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49537232 | TAAAGTAACTGCAAG[A/G]CAAAACCCCAAAACT | 55213 |
rs8001595 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552869 | GCTTGGCTGGACACA[A/T]CTGCGGTAGTGGTAG | 55213 |
rs8001878 | snp | C/G | 0.429987 | 0.173507 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552769 | GTGGAGATTGGAGCA[C/G]AGCTGAAGGATGAAG | 55213 |
rs9316458 | snp | C/T | 0.0962929 | 0.197165 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49555145 | GTAGTTCTACAAGGA[C/T]TTCATCAGTTAATTT | 55213 |
rs9316460 | snp | C/T | 0.432651 | 0.170701 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565383 | cctccacctcccagc[C/T]gcctgccttggcctc | 55213 |
rs9526573 | snp | C/T | 0.499053 | 0.0217445 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539068 | AGAGACAGGGTTTCA[C/T]CATGTTGGCCAGGCT | 55213 |
rs9526577 | snp | C/G | 0.240765 | 0.249829 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563552 | cctctaattgtactt[C/G]ggaggctgaggcatg | 55213 |
rs9535258 | snp | A/G | 0.488846 | 0.0738428 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534508 | CTTCAAAACACACAC[A/G]CGCGCGCACACACAC | 55213 |
rs9535259 | snp | C/G | 0.309648 | 0.24278 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49536350 | AGTTCACCAGAGAGT[C/G]GCACAGTCAAGCTGA | 55213 |
rs9535260 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539017 | tgggattacaggtac[A/G]caccaccacacccag | 55213 |
rs9535261 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541481 | AGAACAAAAAAGCCT[A/G]TGGTCATAAACTAGG | 55213 |
rs9535262 | snp | C/T | 0.245916 | 0.249967 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560558 | AAGGAAACAAAAGTC[C/T]CAGGGCTTCTTTGAA | 55213 |
rs9535263 | snp | A/T | 0.498693 | 0.0255257 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563227 | caacatggtgagacc[A/T]catctctacaaaaaa | 55213 |
rs9535264 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574700 | aaaaaaaaaaaaaaa[A/C]attagaattatatta | 55213 |
rs9562892 | snp | C/T | 0.147321 | 0.227941 | downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49531722 | ATTAAACAAGTTCCC[C/T]ATTCTCCTCTCCCCT | 55213 |
rs9562893 | snp | C/T | 0.429987 | 0.173507 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551774 | gtgtggtggcggcca[C/T]ctgtagtcccagcta | 55213 |
rs9562894 | snp | C/T | 0.429837 | 0.173662 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49556257 | GCTGGAGTGCAGTGG[C/T]GCGATCTCAGCTCAC | 55213 |
rs9562895 | snp | C/T | 0.429837 | 0.173662 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49556425 | TCGATCTCCTGACCA[C/T]GTGGTCCACCCATCT | 55213 |
rs9562896 | snp | A/T | 0.145642 | 0.227177 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49562538 | aaaaaaaaaaaaaTT[A/T]GGAAGATCACTCCAG | 55213 |
rs9562897 | snp | C/T | 0.432357 | 0.171014 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563400 | AGGCACAGTGGCTTA[C/T]GCTTATAATCCCAGC | 55213 |
rs9562898 | snp | C/T | 0.432357 | 0.171014 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563514 | CTAAAAACACAAAAA[C/T]TAGCCAGGCATGGTA | 55213 |
rs9562899 | snp | C/T | 0.346604 | 0.230581 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49567140 | AACGAAACTAGGTTT[C/T]AAGAGACTCTTACCT | 55213 |
rs9562900 | snp | A/G | 0.341251 | 0.232761 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49567226 | CTTCCGAATAGACGC[A/G]ATCTCTTGAGGGGAG | 55213 |
rs9562901 | snp | A/G | 0.441705 | 0.160466 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568854 | gaatcacttgaaccc[A/G]ggaggcggaggttgc | 55213 |
rs9562902 | snp | A/G | 0.444533 | 0.157025 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569438 | AAAAAAAGGCCAGGC[A/G]CGGTAGCTCACTCCT | 55213 |
rs9562903 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49572160 | ggtgaaaccctgcct[C/T]tacaaaaaatacaga | 55213 |
rs9568240 | snp | G/T | 0.149999 | 0.229128 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49532425 | TACTGAAGTTCACAT[G/T]TTGCTCAGATCATAA | 55213 |
rs9568241 | snp | A/T | 0.411578 | 0.190768 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533782 | CGTGGCCCAGGAGAG[A/T]TGCTGCCAACTTCCC | 55213 |
rs9568242 | snp | C/T | 0 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539289 | cagactctggggaAT[C/T]ACACTTATTTGGAGT | 55213 |
rs9568243 | snp | C/T | 0.423726 | 0.179776 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49544400 | CTTAAACCCGGGAGG[C/T]AGAGGTTGCGGTGAG | 55213 |
rs9568244 | snp | A/C | 0.0825414 | 0.185628 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49545854 | ACTCCTAGAGGAGGG[A/C]CAACAGCTAAAACCT | 55213 |
rs9568245 | snp | A/G | 0 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49547754 | AGATAGAAAGAAAGA[A/G]GATGGGGTTAATGTG | 55213 |
rs9568246 | snp | C/T | 0.345959 | 0.23085 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551486 | GCAAGTAAATTGAAA[C/T]GGTTACCATTAGCAG | 55213 |
rs9568247 | snp | C/T | 0.430136 | 0.173352 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551542 | TCTACTTAAAGGCTA[C/T]AGCCAGCTTCTGCAG | 55213 |
rs9568248 | snp | A/G | 0.429987 | 0.173507 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551654 | GCCTGTAATCCCAGC[A/G]CTTTGGGAGGCCGAG | 55213 |
rs9568249 | snp | C/G | 0.430285 | 0.173197 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552963 | CCAGCGTGGGCAGAT[C/G]ACCAGGTCAGGAGAT | 55213 |
rs9568250 | snp | A/C | 0.429987 | 0.173507 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552966 | GCGTGGGCAGATCAC[A/C]AGGTCAGGAGATCGA | 55213 |
rs9568251 | snp | C/T | 0.429987 | 0.173507 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553774 | TTAAAGGCACTTTCA[C/T]CCAGTGCCAGAAGTG | 55213 |
rs9568252 | snp | C/T | 0.429987 | 0.173507 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554378 | ATAAGAGAAGAATAC[C/T]GGAATGGAGGATATT | 55213 |
rs9568253 | snp | A/G | 0.430136 | 0.173352 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554500 | CTAAAGCACCCTAGC[A/G]CAGGGGTCCCCAGTC | 55213 |
rs9568254 | snp | C/T | 0.429987 | 0.173507 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49556792 | ATTCACATAAATATC[C/T]AGTTTAATTATGCAA | 55213 |
rs9568255 | snp | G/T | 0.429987 | 0.173507 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49556877 | ATCAGGAACCCAGCC[G/T]GCATAAATTAGCAAG | 55213 |
rs9568256 | snp | G/T | 0.429987 | 0.173507 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49556939 | CACTTCTCAAATACA[G/T]CACATTCCCTTGCAG | 55213 |
rs9568257 | snp | A/C | 0.390277 | 0.206936 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559185 | gcacttactatatgt[A/C]tccaatggaatatta | 55213 |
rs9568258 | snp | A/C | 0.429538 | 0.173972 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49561327 | CGAAGACAGCCCACA[A/C]AAACTCAGAGTCCTC | 55213 |
rs9568259 | snp | A/G | 0.429538 | 0.173972 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49561594 | GCATACCTTGTTCTT[A/G]GATGGGAAAATTCAG | 55213 |
rs9568260 | snp | A/C | 0.429388 | 0.174127 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49561729 | ATGGGAAGAATAAAC[A/C]AACAAGAATAAATAG | 55213 |
rs9568261 | snp | C/T | 0.0998734 | 0.199905 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49561985 | GCGCGCACCTGTAAT[C/T]CCAGCTACTCAGGAG | 55213 |
rs9568262 | snp | A/G | 0.5 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49562774 | CGTGCCACCATCCCC[A/G]GCTTTTTTTTTTTTT | 55213 |
rs9568263 | snp | C/T | 0.5 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49562777 | GCCACCATCCCCGGC[C/T]TTTTTTTTTTTTTTT | 55213 |
rs9568264 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563233 | ggtgagacctcatct[C/T]tacaaaaaaatttaa | 55213 |
rs9568265 | snp | C/T | 0.39527 | 0.203462 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563257 | AATTTAAAAATGAGG[C/T]GGGAAGATCGCTTGA | 55213 |
rs9568266 | snp | A/G | 0.441432 | 0.160792 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564898 | tccgtctcaaaaaaa[A/G]aaagaaagaaagaaa | 55213 |
rs9568267 | snp | A/G | 0.109814 | 0.206997 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569852 | GTCAAGGCTGCAGTT[A/G]AGCCGAGATCACAAC | 55213 |
rs9568268 | snp | A/G | 0.444533 | 0.157025 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569879 | CAACGCTGCACTCTA[A/G]CCTGGGTGACAGAGG | 55213 |
rs9568269 | snp | C/T | 0.186421 | 0.24178 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49584006 | ATATCATCATCATAA[C/T]AAAGGTCCTCACTTT | 55213 |
rs9591271 | snp | A/G | 0.357664 | 0.225629 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538997 | GCCTCAGCCTCCCGA[A/G]TAGCTGGGATTACAG | 55213 |
rs9591272 | snp | A/G | 0.284995 | 0.247539 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539015 | gctgggattacaggt[A/G]cgcaccaccacaccc | 55213 |
rs9591273 | snp | C/T | 0.284995 | 0.247539 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539016 | ctgggattacaggta[C/T]gcaccaccacaccca | 55213 |
rs9591276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49550014 | ttcttttttgagaca[A/G]gatctcactccgtca | 55213 |
rs9591278 | snp | C/T | 0.431916 | 0.171483 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565798 | aacaggccatgatga[C/T]gatggcggtttcgtc | 55213 |
rs9591279 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565814 | gatggcggtttcgtc[A/G]aatagaaaaggggga | 55213 |
rs9591280 | snp | G/T | 0.375996 | 0.215928 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565972 | ccttacccccaacct[G/T]gtgctctctgaaacg | 55213 |
rs9591281 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566069 | tgaaggcagcatgct[C/T]gttaagagtcatcac | 55213 |
rs9596134 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534363 | ATCTCTCACCCTCCC[C/T]CAGAAAAGATATTTG | 55213 |
rs9596135 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49537377 | TTATCCCATTACGCA[A/G]AAAACATTTGTCAGC | 55213 |
rs9596137 | snp | C/T | 0.162909 | 0.23434 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542299 | TTAGCACCCAAAAAA[C/T]ATTCCACATGCAAGT | 55213 |
rs9596139 | snp | C/T | 0.429238 | 0.174281 | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49549225 | taattgcatgttatg[C/T]gaatttgatatcaat | 55213 |
rs9596140 | snp | A/G | 0.423726 | 0.179776 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49550166 | GTATTTTTTATAGAG[A/G]CAGAGTCTCGCTATA | 55213 |
rs9596141 | snp | A/G | 0.429987 | 0.173507 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554251 | TGCATGAAACTATTA[A/G]CAAGATTGGGAAAAG | 55213 |
rs9596142 | snp | A/G | 0.429987 | 0.173507 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554538 | CATGAGCCGCAGGCC[A/G]GTACCAGTCCGTGCC | 55213 |
rs9596143 | snp | A/G | 0.429987 | 0.173507 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554589 | CAGCAGGAGGTGAGC[A/G]GCGGGCAAGGGAGTA | 55213 |
rs9596144 | snp | G/T | 0.429987 | 0.173507 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554618 | TATTACTGCCTGAGC[G/T]CCACCTCCTGTCAGA | 55213 |
rs9596145 | snp | A/T | 0.429987 | 0.173507 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554647 | GATCAATGGCAGCAT[A/T]AGATTCTCACAGGAG | 55213 |
rs9596148 | snp | C/T | 0.429388 | 0.174127 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49561172 | GGTAATAAAACATCC[C/T]GACCTATTAAGGACA | 55213 |
rs9596150 | snp | C/T | 0.432357 | 0.171014 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564173 | CAAGAACCTATCAAC[C/T]TGCATCCCCGGTTCT | 55213 |
rs9596151 | snp | A/G | 0.432357 | 0.171014 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564286 | AGCCAGGTAGCATCT[A/G]TGTTTAGAAAAATGT | 55213 |
rs9596152 | snp | A/G | 0.42574 | 0.177808 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564878 | cctgggcgacagaga[A/G]agactccgtctcaaa | 55213 |
rs9596153 | snp | C/T | 0.375996 | 0.215928 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565971 | accttacccccaacc[C/T]ggtgctctctgaaac | 55213 |
rs9596154 | snp | A/G | 0 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566124 | ggacacaaacactgc[A/G]gtaggccgcagggtc | 55213 |
rs10589336 | in-del | -/TA | 0.5 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548594 | AAACAAAATATGGTG[-/TA]TATATATATAATGGA | 55213 |
rs10640169 | in-del | -/AC | 0.499234 | 0.0195537 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538758 | TGAATATATATATAT[-/AC]ACACACACACACACA | 55213 |
rs10710755 | in-del | -/A | 0 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564609 | AAAAAAAAAAAAAAA[-/A]TGCCGGGCGCGGTGG | 55213 |
rs10712119 | in-del | -/A | 0.447809 | 0.152878 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551900 | GGGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 55213 |
rs11148150 | snp | C/T | 0.444533 | 0.157025 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49570410 | AGTCAATTCAAGAAA[C/T]AGGTCATGTATCTTA | 55213 |
rs11148151 | snp | A/G | 0.4444 | 0.15719 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49570477 | CAACAGGCTTGGTAG[A/G]GTGGTAACAACAGAG | 55213 |
rs11148152 | snp | G/T | 0.444533 | 0.157025 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573518 | CTGTGGCACGATCTT[G/T]GCTCACTGCAATCTC | 55213 |
rs11148153 | snp | C/T | 0.444533 | 0.157025 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573621 | GCCCGGCTAATTTTG[C/T]ATTTTTTTAGTAGAG | 55213 |
rs11148154 | snp | G/T | 0.444533 | 0.157025 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573655 | GGGTTTCACCATGTT[G/T]GCCAGGCTGGTCTCA | 55213 |
rs11148155 | snp | A/G | 0.116838 | 0.211584 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49579541 | aggcaggagaatggc[A/G]tgagcccaggaggca | 55213 |
rs11148156 | snp | C/T | 0.212425 | 0.24716 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49582284 | ctgatgtcaggagtt[C/T]gagaccggcctggcc | 55213 |
rs11280548 | in-del | -/AGATAA/TAAAG | | | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49532200 | ATTTAAAAAAAATAA[-/AGATAA/TAAAG]TCAAATGCTTTTTGA | 55213 |
rs11285149 | in-del | -/A | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542214 | GCAAAACTCCGTCTC[-/A]AAAAAAAAAAAAAAG | 55213 |
rs11310875 | in-del | -/T | 0.26326 | 0.249648 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49577534 | TAGTTTAAATTGCTG[-/T]TATGTACTGGCTTTT | 55213 |
rs11311610 | in-del | -/A | 0.444799 | 0.156695 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569420 | TTCTACAAAAAATAC[-/A]AAAAAAAAAGGCCAG | 55213 |
rs11378020 | in-del | -/A | 0.5 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557757 | CTCTACAAAAAAAAA[-/A]TTTTTTTTTTAAAAG | 55213 |
rs11420011 | in-del | -/T | 0.261884 | 0.249717 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49584268 | AATCACTTGCAAAAA[-/T]TCTCTTTAAAGATGA | 55213 |
rs11458278 | in-del | -/A/AAAA | 0 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559672 | AAAAAAAAAAAAAAA[-/A/AAAA]GAAAGTTGTTGTCAG | 55213 |
rs11616671 | snp | G/T | 0.5 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573506 | caagctggagtgctg[G/T]ggcacgatcttggct | 55213 |
rs11616920 | snp | A/G | 0.429987 | 0.173507 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49558833 | gtgtggcagtaggag[A/G]tgccccttgtaattt | 55213 |
rs11620126 | snp | A/G | 0.212122 | 0.247114 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49579390 | GCACTTTGGGAGGCC[A/G]AGGCAGGCGGATCAC | 55213 |
rs12017701 | snp | C/T | 0.432357 | 0.171014 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49562673 | gctggagtgcagtgg[C/T]gcaatcatagctcac | 55213 |
rs12019951 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49544481 | TCTCAAAGAAACAAA[C/G]AAACAAACAAACAAA | 55213 |
rs12146924 | snp | C/T | 0.498734 | 0.0251279 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560222 | TCTATTAAGTAACCA[C/T]GGACAGAGTAAAGGA | 55213 |
rs12428300 | snp | A/G | 0.163236 | 0.234461 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559428 | tttggaggccaaggc[A/G]ggcagatcacgaggt | 55213 |
rs12428301 | snp | A/G | 0.380138 | 0.213458 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559453 | cgaggtcaggagatc[A/G]agaccatcctggcta | 55213 |
rs12428474 | snp | A/T | 0.429837 | 0.173662 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49555882 | TACCCACTTTATACA[A/T]CTCCGTTTTATACAT | 55213 |
rs12429331 | snp | C/T | 0.350327 | 0.228986 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568093 | AATTCCTTCTGGAAA[C/T]AGTGCTCATGGAAGC | 55213 |
rs12429350 | snp | C/G | 0.142609 | 0.225759 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568327 | AATTCCAGTCTTTTG[C/G]TAGAACAATAGTGCA | 55213 |
rs12429621 | snp | A/C | 0.162909 | 0.23434 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541268 | CATTTTGTTTCTAAA[A/C]CGCTAAATGCATTAG | 55213 |
rs12430435 | snp | C/T | 0.497641 | 0.0342639 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568364 | GCCTGCACATTATTG[C/T]ATTGACATGTCTTGT | 55213 |
rs12430943 | snp | C/T | 0.444533 | 0.157025 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49570012 | TAAGAAGTCAAGCCA[C/T]ATAAAGCCATACAAG | 55213 |
rs12431331 | snp | A/G | 0.493703 | 0.0557558 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568459 | TATTTTACTGTTACT[A/G]GCTATTAATATTTCA | 55213 |
rs12560813 | snp | A/G | 0.445724 | 0.155538 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574150 | GGTGgacagagtctc[A/G]ctctgttgcccagtc | 55213 |
rs12561469 | snp | C/T | 0.444533 | 0.157025 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573907 | ttgtgcctcagcctc[C/T]cgagtagctggaatt | 55213 |
rs12561475 | snp | A/G | 0.444533 | 0.157025 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574135 | TTTTTGGGGGTGGGG[A/G]GTGgacagagtctca | 55213 |
rs12583466 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565623 | ggagcgcctctgccc[A/C]gccccgaccccgtct | 55213 |
rs12583946 | snp | A/G | 0.429388 | 0.174127 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560369 | TTAGGCTTTCTAAAA[A/G]CTTTGATTCATCTCA | 55213 |
rs12584718 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49544645 | GACATTTCTCTCTAC[C/T]ACCAAGGCTATTTTT | 55213 |
rs12585072 | snp | A/G | 0.429987 | 0.173507 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49558419 | caaagtaggcttgtc[A/G]tggtggctatgcctg | 55213 |
rs12585079 | snp | A/C | 0.429688 | 0.173817 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49558508 | accagcctggccaac[A/C]tggtgaaaccccgtc | 55213 |
rs12585829 | snp | A/G | 0.243347 | 0.249911 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49579611 | TTTGGGTGACAGATC[A/G]AGACTTGTCTCAGAA | 55213 |
rs12875103 | snp | A/G | 0 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49550187 | tctcgctatattgcc[A/G]gggccggtcaccaac | 55213 |
rs12875236 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49550167 | tattttttatagaga[A/C]agagtctcgctatat | 55213 |
rs12875253 | snp | C/T | 0 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49550204 | ggccggtcaccaact[C/T]ctgggctcaagtgat | 55213 |
rs12876188 | snp | A/C/T | 0.0023933 | 0.0345097 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49550152 | cccggctaagttttg[A/C/T]attttttatagagac | 55213 |
rs12877372 | snp | A/G | 0.499713 | 0.0119774 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568654 | TAATCAggccggggg[A/G]ggggggtggctcaca | 55213 |
rs13378385 | snp | G/T | 0.495174 | 0.0488838 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49585169 | GCACCTCAAAAAAGA[G/T]AGGGAGGCAGGGAAA | 55213 |
rs13378867 | snp | A/T | 0.495291 | 0.0482933 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49585170 | CACCTCAAAAAAGAG[A/T]GGGAGGCAGGGAAAA | 55213 |
rs17069321 | snp | A/G | 0.100231 | 0.200173 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49540122 | AAACCAACCATACCC[A/G]CCTTCAGCTCACTGA | 55213 |
rs17069328 | snp | C/T | 0.429238 | 0.174281 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49561068 | TTATCTCTTGAAGTA[C/T]CATCGTTTCAGGCAT | 55213 |
rs17073094 | snp | A/G | 0.00795532 | 0.062565 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533891 | CCAGCCCAAATTTAC[A/G]AAAGGTCACATTTAA | 55213 |
rs17073103 | snp | C/T | 0.0973687 | 0.197999 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535435 | TCTTATCACAAATAG[C/T]TTGACTTTATTACAA | 55213 |
rs17073112 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542435 | CTGTTTCCATTTGAT[C/G]GTCCCCAAGATTTTT | 55213 |
rs17073145 | snp | C/T | 0.34429 | 0.231537 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49559963 | ATGTGAGCCACAAGC[C/T]ACTTCCACCACTTGC | 55213 |
rs17073150 | snp | A/G | 0.339123 | 0.233575 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49560014 | GACCTGGACGGGAGC[A/G]ATGCCTTGGTTGGTC | 55213 |
rs17073175 | snp | C/T | 0.164873 | 0.23506 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49567571 | TTCCTAGTCAGTGCT[C/T]ATCTGTTCCACATGT | 55213 |
rs17073188 | snp | G/T | 0.243633 | 0.249919 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49570061 | GAAAATCCAGAAGCA[G/T]GTTTTCCTGGAATTA | 55213 |
rs17853794 | snp | A/G/T | 1.6473e-05 | 0.00286988 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49560010 | TACAGACCTGGACGG[A/G/T]AGCAATGCCTTGGTT | 55213 |
rs28410026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49547436 | ATTAATTTTCAAGCA[C/T]AGAGCATCATGACCC | 55213 |
rs28682474 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49549024 | TGTAGTCTTACTACT[C/T]GGGAGGCTGAGGCAG | 55213 |
rs34012536 | in-del | -/AGAC | 0.361263 | 0.223876 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535566 | CGAGGTGGGAATGTT[-/AGAC]AGAGTGGAAGGGGCC | 55213 |
rs34214528 | in-del | -/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557972 | AAAAAATCCAAACAT[-/C]CCATGAACAGATGAA | 55213 |
rs34222928 | in-del | -/A | 0.487432 | 0.0782705 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49532415 | ATAGTAAACATACTG[-/A]AGTTCACATTTTGCT | 55213 |
rs34402585 | in-del | -/AC/CA | 0 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538759 | ACACACACACACACA[-/AC/CA]TATATATATATGCCC | 55213 |
rs34449946 | snp | A/G | 0.11228 | 0.208646 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49556442 | TGGTCCACCCATCTC[A/G]GCCTCCCAAAGTGCT | 55213 |
rs34676232 | in-del | -/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49547612 | AATGGACTCTTAAAG[-/C]AAGACAATATTCAGA | 55213 |
rs34972735 | in-del | -/A | 0.380569 | 0.213194 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49575435 | ATAAATTGTTCTACC[-/A]AAAAAAAAAAAAATG | 55213 |
rs35014325 | in-del | -/A | | | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49540628 | TATGTTCCAACCTGC[-/A]AGCACAGCTGCTAGG | 55213 |
rs35069541 | in-del | -/A/TA | 0.498277 | 0.0293024 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539178 | CATTTTTTTTTTTTT[-/A/TA]AAGCACACCTTCATG | 55213 |
rs35078637 | in-del | -/A | 0.5 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564891 | GAGAGACTCCGTCTC[-/A]AAAAAAAAAAGAAAG | 55213 |
rs35171419 | snp | C/T | 0.021333 | 0.101051 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49558773 | AACAACACAGTCAAA[C/T]ACCCTCAGTGAGCTG | 55213 |
rs35414732 | in-del | -/A | 0.443598 | 0.158176 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586740 | CCAGGGCCAATGATT[-/A]AAAAAAAAAAAAAAA | 55213 |
rs35464822 | in-del | -/A | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49579977 | CTTTAGCCCCATCAT[-/A]CCAAGGGGCTGCTTT | 55213 |
rs35472053 | snp | A/G | 0.496583 | 0.0411924 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568507 | GTAGTGGCCATATAT[A/G]AAATCACCATGGATG | 55213 |
rs35677742 | in-del | -/C | | | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49540468 | GCAGAGCGTACACAG[-/C]ATACAAATCATACAC | 55213 |
rs35734605 | snp | C/T | 0.0648419 | 0.167978 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49575513 | ATCAACCTAGGTGCC[C/T]GTTGACAGTAGATTG | 55213 |
rs35741686 | in-del | -/T | 0 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573788 | CTTTTTTTTTTTTTT[-/T]GAGACAGAGCCTCGC | 55213 |
rs35758245 | in-del | -/AG | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559359 | CAAACTCAAAGAAAC[-/AG]AGTAGAAAGTTGTTG | 55213 |
rs35859795 | in-del | -/C | | | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49582206 | AGTGCAACAGAAGCG[-/C]CCGGGCGCAGTGGCT | 55213 |
rs35882019 | in-del | -/A | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551318 | AGACGTGGCACAGCC[-/A]AAGTTACCTTTCTTT | 55213 |
rs35919905 | in-del | -/G | | | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49587566 | AGGGACCACAAATCA[-/G]GGGAGTCAGGGAGAA | 55213 |
rs35944402 | in-del | -/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49567947 | GTAAAAGATTTGACA[-/G]GGGGAGTAATACATG | 55213 |
rs35992025 | in-del | -/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49575616 | GCTACAGGCCATTAT[-/C]CCTATGTGAATTAAC | 55213 |
rs36063817 | in-del | -/T | 0.5 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539165 | CTCCAAGCCTGGCCA[-/T]TTTTTTTTTTTTTAA | 55213 |
rs41284782 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49532604 | AGAAAAGGGGGCTGG[A/G]GCTCCTAGGCTTGTA | 55213 |
rs41284784 | snp | A/G | 0.00438332 | 0.0466095 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49532646 | TATCAGTGAATTCCT[A/G]TCTTTAGGGCCTCAC | 55213 |
rs41284786 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533206 | CATATATAGTAGATA[C/T]GATGATTCAGCAGTC | 55213 |
rs41284788 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533307 | GGTGGTGGGGGACAA[A/T]TTAAACTTGAGTTCT | 55213 |
rs41284790 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533775 | GTTGATACGTGGCCC[A/G]GGAGAGTTGCTGCCA | 55213 |
rs41284792 | snp | C/T | 0.0160639 | 0.0881696 | synonymous-codon, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49544862 | TAAAAAGTCTTCATG[C/T]TCTGAAGGCAACAAA | 55213 |
rs41284794 | snp | A/G | 0.0380402 | 0.132563 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549492 | CGAGACGGCGGGAGT[A/G]GCAAAGCAGGCAAAC | 55213 |
rs41284796 | snp | A/G | 0.000381683 | 0.0138093 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549615 | CTTGGCTGCAGACGT[A/G]TGGGCAGAGTGACAG | 55213 |
rs41284798 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552105 | TGACTGAAGAGTAAA[C/T]CTCCAATATTTCTCC | 55213 |
rs45490794 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560213 | CCCCTCCTCTCTATT[A/G]AGTAACCATGGACAG | 55213 |
rs55875979 | in-del | -/AA | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49562534 | AAAAAAAAAAAAAAA[-/AA]TTTGGAAGATCACTC | 55213 |
rs55966740 | snp | C/T | 0.211516 | 0.24702 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573258 | GTATACACCAAAATA[C/T]ATCTCCATGGAGAGA | 55213 |
rs56131732 | in-del | -/ACTC | 0.00636936 | 0.0560724 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566974 | ACTCAGAGTGCTATG[-/ACTC]GAGTAGACGGGTATT | 55213 |
rs56213457 | snp | C/T | 0.432063 | 0.171327 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563347 | ACAGAGAGAGAGAGA[C/T]CCTGCCTCAAAAAAA | 55213 |
rs56225299 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565269 | TGATCTGCCAGCCTC[A/G]GCCTCCCGAGGTGCC | 55213 |
rs56229283 | snp | A/G | 0.444666 | 0.15686 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574253 | CCTTCTGAGTGGCTG[A/G]GATTACAGGTGTGCA | 55213 |
rs56250426 | snp | A/G | 0.429238 | 0.174281 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560732 | TGTGTGTGATCTCAG[A/G]AAGATTAAAAGGCTG | 55213 |
rs56289138 | snp | A/G | 0.4444 | 0.15719 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49576749 | TTGCAAGCCTTCCAT[A/G]TTTTATTTAGGAAAT | 55213 |
rs56319255 | snp | C/T | 0.345925 | 0.230864 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49561096 | CATTTCTTTCCACAG[C/T]ACCCCCGAGTGCCAA | 55213 |
rs56354206 | in-del | -/C | 0.261884 | 0.249717 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49582825 | AGGTCACCTATTTTT[-/C]CCCTATGAAGAAAGA | 55213 |
rs56376799 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564897 | CTCCGTCTCAAAAAA[A/G]AAAAGAAAGAAAGAA | 55213 |
rs56850432 | snp | G/T | 0.432357 | 0.171014 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563661 | GAGACTGTCTCAAAA[G/T]AAAAAAAAGGAAAGA | 55213 |
rs56856971 | snp | A/G | 0.11228 | 0.208646 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49543124 | AAAAATTAGCTGGGC[A/G]TGGTTAGTGCACGAT | 55213 |
rs56970196 | in-del | -/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49556214 | TTTTTTTTTTTTTTT[-/T]GAGATAGAGTTTCAC | 55213 |
rs56994102 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548166 | GGAGGCTGAGGCGGG[C/T]GGATCACGAGGTCAG | 55213 |
rs57519002 | in-del | -/TGAC | 0 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535015 | TCTAGCCTGGGTGAC[-/TGAC]AGAGCAGAGGCTCTG | 55213 |
rs57586924 | in-del | -/A | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563380 | AAAAAAAAAAAAAAA[-/A]GGCCAGGCACAGTGG | 55213 |
rs57604202 | snp | G/T | 0.391954 | 0.205789 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551961 | CTGAATTTTTCCATT[G/T]TTTTTTTTTTTTTTA | 55213 |
rs57650425 | snp | A/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541009 | AAATCCAGAAGACCT[A/T]AAAGTAAAATATGTG | 55213 |
rs57776599 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548158 | GCACTTTGGGAGGCT[A/G]AGGCGGGCGGATCAC | 55213 |
rs57855009 | in-del | -/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566265 | TGATCAATAAAAAAA[-/T]AAAATAAAATAAATA | 55213 |
rs57884356 | snp | C/G | 0.0644693 | 0.167566 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559520 | AATTAGGCGGGTGTG[C/G]TGGTGGGTGCCTGTA | 55213 |
rs57945792 | in-del | -/A | 0.43221 | 0.171171 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563657 | GAGCGAGACTGTCTC[-/A]AAAGAAAAAAAAGGA | 55213 |
rs58015266 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565356 | CAGTGGTGTGATCTC[A/G]GCTAGCTACGACCTC | 55213 |
rs58168524 | in-del | -/AACAAACA | 0 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49544495 | ACAAACAAACAAACA[-/AACAAACA]CAAAAAACCAATATG | 55213 |
rs58254547 | in-del | -/AA | 0.432944 | 0.170387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49561930 | AACCCCACATCTACT[-/AA]AAAAAAAAAAAAAAT | 55213 |
rs58258059 | snp | G/T | 0.0433465 | 0.140692 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49587145 | TTCTCCCTTAGATTA[G/T]AAACTCTTTGAAACA | 55213 |
rs58284306 | snp | A/G | 0.0611083 | 0.163768 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546611 | TTCCTACAACTGGAC[A/G]GCCCCATCTGGGGGT | 55213 |
rs58478517 | snp | C/T | 0.030665 | 0.119967 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557408 | AGAAGACAGAATCAA[C/T]AGGATGAGTGACCTT | 55213 |
rs58896397 | in-del | -/TTTTTT | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49562801 | TTTTTTTTTTTTTTT[-/TTTTTT]AAGAGACATGGCCTC | 55213 |
rs58942290 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49579381 | GTAATCCCAGCACTT[C/T]GGGAGGCCGAGGCAG | 55213 |
rs58998549 | in-del | -/A | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566309 | ATAAATAAATAAAAA[-/A]GTTGCATTGCAACAC | 55213 |
rs59088183 | in-del | -/GAGA | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563343 | GGTGACAGAGAGAGA[-/GAGA]CCCTGCCTCAAAAAA | 55213 |
rs59094122 | in-del | -/C | 0.0696718 | 0.173152 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560619 | TGGCTGAATTTTTTT[-/C]TTTTTTTTACATAAA | 55213 |
rs59193351 | in-del | -/A/AA | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49575448 | CAAAAAAAAAAAAAA[-/A/AA]TGCACCTGTATGTTC | 55213 |
rs59194434 | snp | A/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583549 | AGCACGTACACAACA[A/T]GTACTTTTTTTTTTT | 55213 |
rs59416746 | snp | C/T | 0.429987 | 0.173507 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49558689 | AGAAGGGTGAAACTC[C/T]GTCTCCAAAAAAAAA | 55213 |
rs59428512 | snp | A/G | 0.43655 | 0.16643 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565556 | CCCGGCCGCCACCCC[A/G]TCTAGGAAGTGAGGA | 55213 |
rs59572011 | in-del | -/TTTT | 0 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49562803 | TTTTTTTTTTTTTTT[-/TTTT]AAGAGACATGGCCTC | 55213 |
rs59803546 | in-del | -/AAG | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566058 | AACAGATGCTTGAAG[-/AAG]GCAGCATGCTCGTTA | 55213 |
rs59899830 | in-del | -/AAATAAATAAATAAA | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566288 | AATAAATAAATAAAT[-/AAATAAATAAATAAA]TAAAAAAGTTGCATT | 55213 |
rs59921927 | in-del | -/AACA | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49544499 | ACAAACAAACAAACA[-/AACA]CAAAAAACCAATATG | 55213 |
rs59998676 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49550884 | AGGTGGGTAGATCAC[C/T]TGAGGCCAGGAGTTC | 55213 |
rs60042643 | in-del | -/AA | | | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586755 | AAAAAAAAAAAAAAA[-/AA]GGTATTAAGAAACTA | 55213 |
rs60084900 | in-del | -/ATAAG | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552842 | AAGCTAGTTTAGAAG[-/ATAAG]TAGGTGGGCTTGGCT | 55213 |
rs60231483 | in-del | -/T | 0.16618 | 0.23553 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49549990 | CTTAAATACCATTTC[-/T]TTTTTTTTTTCTTTT | 55213 |
rs60482286 | snp | A/G | 0.424037 | 0.179474 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535929 | TCAGGAAGCTGAGGC[A/G]GGAGAATCGCTTGAA | 55213 |
rs60783473 | in-del | -/T | 0.454592 | 0.143673 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560613 | TGAAATCTGGCTGAA[-/T]TTTTTTTTTTTTTTA | 55213 |
rs61071562 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49576224 | TGAGATGATTTTTTT[A/T]AAGTAGTCTAGAGAT | 55213 |
rs61212809 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49580042 | CTCAGCCATGTGCTC[A/G]AAAAGCAAACGAACC | 55213 |
rs61257060 | snp | A/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566258 | CCAAGAATGATCAAT[A/T]AAAAAATAAAATAAA | 55213 |
rs61295710 | in-del | -/TAG | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559363 | CTCAAAGAAACAGAG[-/TAG]AAAGTTGTTGGCTGG | 55213 |
rs61705134 | in-del | -/AATAT | | | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49532269 | ATGACTTAGTAATCT[-/AATAT]GAGAAGTGGTCCTTC | 55213 |
rs61960050 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534890 | ACTACAAAAATTAGC[C/T]GGGCGTGGTGGTGGA | 55213 |
rs61961360 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551146 | AGGGAGAAGGGGGAA[A/G]GGGGAAGCAGGGAGG | 55213 |
rs61961361 | snp | A/G | 0.0501905 | 0.150254 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551151 | GAAGGGGGAAGGGGG[A/G]AGCAGGGAGGGAGAA | 55213 |
rs61961362 | snp | G/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554850 | AGGTTGGGGACCACT[G/T]CCCAAGCACACCAAT | 55213 |
rs61961364 | snp | C/T | 0.429987 | 0.173507 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49558802 | TGTCACATTTGTGAT[C/T]GTTTGCTTTTGAACT | 55213 |
rs61961400 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565472 | CGTCTCTGCCTGGCC[A/G]CCCATGGTCTGGGAT | 55213 |
rs61961401 | snp | C/T | 0.0640965 | 0.167152 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49567885 | ATAACATTTGGATGT[C/T]TTGACAAATGTGTGT | 55213 |
rs61961403 | snp | C/T | 0.445855 | 0.155373 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568574 | AGCGTACTCTCACGG[C/T]ATTTCAGTTTTGTTT | 55213 |
rs61961404 | snp | A/G | 0.444133 | 0.157519 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569521 | GTTCGTGACCAGCCT[A/G]GCAAACATAGTGAAA | 55213 |
rs61961406 | snp | A/C | 0.444799 | 0.156695 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573264 | ACCAAAATATATCTC[A/C]ATGGAGAGATTACAG | 55213 |
rs61961407 | snp | A/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574703 | AAAAAAAAAAAACAT[A/T]AGAATTATATTATCT | 55213 |
rs62637568 | snp | C/T | 0.00978881 | 0.0692718 | synonymous-codon, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49551439 | GCCCTCATCTGTTAG[C/T]GCTAGAGTATGTGCG | 55213 |
rs62637574 | snp | A/G | 0.0109297 | 0.0731122 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549489 | CCACGAGACGGCGGG[A/G]GTGGCAAAGCAGGCA | 55213 |
rs66529613 | in-del | -/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573465 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTTTCGC | 55213 |
rs66531473 | in-del | -/A | 0 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49579625 | CGAGACTTGTCTCAG[-/A]AAAAAAAAAAAAAAG | 55213 |
rs66645127 | in-del | -/A | 0.499992 | 0.00199679 | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49549135 | AGATTCTGTCTCAAT[-/A]AAAAAAAAAAAAAAG | 55213 |
rs67033206 | snp | A/G | 0.207253 | 0.246318 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586282 | CTGAGGCCAGGAGAG[A/G]GACTGCTACGAGCTG | 55213 |
rs67044707 | in-del | -/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574700 | AAAAAAAAAAAAAAA[-/C]ATTAGAATTATATTA | 55213 |
rs67275254 | snp | A/G | 0.344527 | 0.23144 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559884 | TACTATGATGAAAAA[A/G]AAAAAGAATAAAGAA | 55213 |
rs67565206 | snp | A/T | 0 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49558718 | AAAAAAAAAAAAAAA[A/T]TCACAAAGTAGACAA | 55213 |
rs67614990 | in-del | -/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542230 | AAAAAAAAAAAAAAG[-/T]AAGTATATTAACTAC | 55213 |
rs71078860 | in-del | -/C | 0.499891 | 0.00738737 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538889 | AAGTTTTTTTTAACT[-/C]TTTTTTTTTTTTTTG | 55213 |
rs71078861 | in-del | -/A | 0 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539180 | TTTTTTTTTTTTTAA[-/A]GCACACCTTCATGGT | 55213 |
rs71078864 | in-del | -/AA | 0 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563380 | AAAAAAAAAAAAAAA[-/AA]GGCCAGGCACAGTGG | 55213 |
rs71078867 | in-del | -/CA | 0 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574700 | AAAAAAAAAAAAAAA[-/CA]TTAGAATTATATTAT | 55213 |
rs71078868 | in-del | -/A | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49576178 | GGCGACAGGCGTCGC[-/A]AAAAAAAAAAAAAAA | 55213 |
rs71078869 | in-del | -/CCGGCC | 0 | 0 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49585678 | GCCCCGGCCCCGGCC[-/CCGGCC]GAAACCCTGCTCTTC | 55213 |
rs71216548 | in-del | GAAAGATGATAAAGTTTCAC/TTCAA | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533076 | AGGAAAACCAAAAGT[GAAAGATGATAAAGTTTCAC/TTCAA]ATAAGCCAATGTGTG | 55213 |
rs71434474 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571413 | TTCTGCCTAGATTTG[C/T]CTGGTTAAACCTCAT | 55213 |
rs71759933 | in-del | -/GAA | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566055 | TTAAACAGATGCTTG[-/GAA]AAGGCAGCATGCTCG | 55213 |
rs71818417 | in-del | -/CA | 0.0825414 | 0.185628 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546319 | ACACTCAGATGAGAT[-/CA]CAAAGTGAGAGGGAA | 55213 |
rs72049082 | in-del | -/TG | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583387 | GTGTGCTTTTGTGTA[-/TG]TGTGTGTGTGTGTGT | 55213 |
rs72393585 | in-del | -/GACT/TGAC | 0 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535012 | CACTCTAGCCTGGGT[-/GACT/TGAC]GACAGAGCAGAGGCT | 55213 |
rs73190741 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538758 | ATGAATATATATATA[C/T]ACACACACACACACA | 55213 |
rs73190742 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538863 | TTGAATCTGTAATAT[G/T]TGTAGGATTTTAAGT | 55213 |
rs73190743 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538890 | AAGTTTTTTTTAACT[C/T]TTTTTTTTTTTTTGA | 55213 |
rs73190749 | snp | A/G | 0.137057 | 0.223033 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541661 | GGCTCGTCCATCCCA[A/G]TGCTACCACAGTACC | 55213 |
rs73190753 | snp | C/G | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546903 | TGGCCTGGGGTGTGG[C/G]GACCCCTGATCTAGG | 55213 |
rs73190794 | snp | A/T | 0.120326 | 0.21374 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49580870 | CAGGACACAGAGCCA[A/T]CACCAACAGAAATTA | 55213 |
rs73493257 | snp | C/T | 0.0422008 | 0.138995 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533582 | TAAAAAAGTCATCAA[C/T]GCAAGCACACAAACA | 55213 |
rs73493259 | snp | C/T | 0.0501905 | 0.150254 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534529 | GCACACACACACACA[C/T]GCAAGATCTACAAGG | 55213 |
rs73493264 | snp | A/G | 0.0792508 | 0.182605 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49536196 | ATATTCAAAAGTTCC[A/G]AACATTAAAAGCCAA | 55213 |
rs73493297 | snp | C/G/T | 0.0114731 | 0.0748699 | synonymous-codon, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49551451 | TAGTGCTAGAGTATG[C/G/T]GCGTAACCGCAGACA | 55213 |
rs73495237 | snp | C/T | 0.0729998 | 0.176553 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557235 | GCAAGACTGGACAGA[C/T]GGATCAACTTAAAAG | 55213 |
rs73495246 | snp | C/G | 0.0729998 | 0.176553 | intron-variant, missense | RCBTB1 | GRCh38.p7 | 13:49558330 | TGGCCACATGCAACC[C/G]TGAACTGGAACAAAC | 55213 |
rs73495265 | snp | A/G | 0.0711525 | 0.174681 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560896 | CAGGGTAAGGTATGC[A/G]GGGATGAGGGGTGCA | 55213 |
rs73495297 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49575853 | TCACACGCTATACCC[A/G]TGTAACAAACCTGCA | 55213 |
rs73495301 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49576444 | ATATAGAAAGGTTTC[A/G]GTCCTAAAAAATGTG | 55213 |
rs73497213 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49584953 | GTCCTCACTAACAAA[A/C]TCCCTGCCTTTGTGG | 55213 |
rs74076080 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant, utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49550412 | CAAGCCAAACTTACT[A/G]TATTTCTCAGTAGTA | 55213 |
rs74077934 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49570970 | CTCAACAACTTCAGT[C/G]AACTTCCTAAAGTCA | 55213 |
rs74077939 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581923 | GCAGCAGGTTGAGGC[A/G]TATGTGAAAGGTGAA | 55213 |
rs74077942 | snp | A/G | 0.00636936 | 0.0560724 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49587476 | ATGGTTGCTGATAAG[A/G]AATGTGTAGTCTGGT | 55213 |
rs74263278 | in-del | -/GTGT | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583410 | TGTGTGTGTGTGTGT[-/GTGT]TTTAAATGTGATCTA | 55213 |
rs74421029 | snp | A/G | 0.0718919 | 0.175435 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546509 | TTTATTGTGCACTTA[A/G]TTTTTATTATTGTTA | 55213 |
rs74435421 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568625 | TGAGTGGAGTTGGAT[A/G]TCACTTAAAAAAATA | 55213 |
rs74494709 | snp | C/T | 0.0030468 | 0.0389117 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49544874 | ATGCTCTGAAGGCAA[C/T]AAACATATATTAATA | 55213 |
rs74585440 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564172 | ACAAGAACCTATCAA[C/G]CTGCATCCCCGGTTC | 55213 |
rs74709344 | snp | G/T | 0 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573800 | CTCTTTTTTTTTTTT[G/T]TGAGACAGAGCCTCG | 55213 |
rs74796370 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539299 | GGAATCACACTTATT[C/T]GGAGTCTTTCTAAAG | 55213 |
rs74801960 | snp | C/G | 0.0402882 | 0.136092 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551525 | GAAGGGCAGGGAGAA[C/G]ATCTACTTAAAGGCT | 55213 |
rs74813761 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563930 | AGACAAAGAAAGGCC[A/G]GGATGCAAATCATCT | 55213 |
rs74851694 | snp | A/G | 0.0629771 | 0.165899 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538749 | ATACAAATTATGAAT[A/G]TATATATATACACAC | 55213 |
rs74855677 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49576414 | ATAAACTCAAAGATA[C/T]ATTTCTAAAATTAAA | 55213 |
rs74929591 | snp | C/G | 0.0441095 | 0.141807 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49577878 | TTTTAATTGCAAAAA[C/G]TTTGAATTAAAGCAT | 55213 |
rs75037063 | snp | A/G | 0.5 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542231 | AAAAAAAAAAAAAGT[A/G]AGTATATTAACTACT | 55213 |
rs75081475 | snp | C/T | 0.0629771 | 0.165899 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534511 | CAAAACACACACGCG[C/T]GCGCACACACACACA | 55213 |
rs75091607 | snp | G/T | 0.5 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542718 | CTCCTTTTTTTTTTT[G/T]GCATTGCCTGTTCCC | 55213 |
rs75212418 | snp | A/C | 0.5 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574601 | GCAAAATCTGGAAAA[A/C]TGAATTATTAATATA | 55213 |
rs75247037 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552673 | AGCAAGTGCTACAAT[A/G]GGTATAATCAAGGCG | 55213 |
rs75264173 | snp | A/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564168 | AAGGACAAGAACCTA[A/T]CAACCTGCATCCCCG | 55213 |
rs75295570 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553999 | GACATGTTCATCAGT[A/G]GAGCTCTGTATGTGG | 55213 |
rs75328996 | snp | A/C | 0 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49536024 | GTGAAACTCCATCTC[A/C]AAAAAAAAAAAAAAG | 55213 |
rs75419616 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49543555 | TTGCCAATAGGTTTT[C/T]ACCTAAATTTCCAAA | 55213 |
rs75601296 | snp | A/T | 0.243633 | 0.249919 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49578824 | TCATAGCCTTCTTCC[A/T]TTTTTAGCAATAAAT | 55213 |
rs75721817 | snp | C/G | 0.0217236 | 0.101931 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553997 | CTGACATGTTCATCA[C/G]TAGAGCTCTGTATGT | 55213 |
rs75779777 | snp | A/G | 0.5 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548595 | AACAAAATATGGTGT[A/G]TATATATATAATGGA | 55213 |
rs75881673 | snp | C/T | 0.0569829 | 0.158885 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533534 | AACAGGTTTAATATA[C/T]GTTAAACTTATTACT | 55213 |
rs75896169 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581393 | GCAGACGCTGAGCTT[A/G]AGTGAGAGAGAACTG | 55213 |
rs76012205 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49584664 | CTTTTAGTCCTCCCA[A/G]AAAAAGAATAGGGCA | 55213 |
rs76117011 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571009 | TGACTTTATCTTGCC[G/T]TGTAAATGTACAGCA | 55213 |
rs76175523 | snp | A/T | 0.243347 | 0.249911 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581906 | GTGGAAGAGGCCAGG[A/T]TGCAGCAGGTTGAGG | 55213 |
rs76288853 | snp | A/C | 0 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548388 | AGTGAGACTCCGTCT[A/C]AAAAAAAAAAAAAAA | 55213 |
rs76333026 | snp | A/C | 0 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49558699 | AACTCTGTCTCCAAA[A/C]AAAAAAAAAAAAAAA | 55213 |
rs76356907 | snp | C/T | 0.0547245 | 0.156101 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49537801 | CTCCTTTGTGAAGTC[C/T]TTCTTAATAAAACTT | 55213 |
rs76477280 | snp | A/G | 0.0763149 | 0.179815 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573044 | TGGTTTGTCCAAATT[A/G]TAAGCACCCCCCAAG | 55213 |
rs76543201 | snp | C/G | 0 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571139 | ATCATCTGAGGTCAG[C/G]AGTTCGAGACTAGCT | 55213 |
rs76646184 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49575265 | ACAAAAGATATTGGC[A/G]AGGCTGTACAGCAGA | 55213 |
rs76702043 | snp | A/C | 0.5 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49558695 | GTGAAACTCTGTCTC[A/C]AAAAAAAAAAAAAAA | 55213 |
rs76717572 | snp | A/G | 0.039522 | 0.134904 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583262 | GAAAGAGCACTGAGC[A/G]GAGAAACCTAGCAGG | 55213 |
rs76845091 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49561437 | CTGAGAAAGATGAGG[C/T]TTAAGACTGAAAGAA | 55213 |
rs76874066 | snp | A/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539178 | CCATTTTTTTTTTTT[A/T]AAGCACACCTTCATG | 55213 |
rs76981568 | snp | C/T | 0.040671 | 0.13668 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49561312 | TTGTCTACTGTAGAA[C/T]GAAGACAGCCCACAC | 55213 |
rs77036104 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49550639 | ATATTACACCATAAA[A/C]ATCAACATGGCCATA | 55213 |
rs77080875 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49556935 | CTGGCACTTCTCAAA[C/T]ACATCACATTCCCTT | 55213 |
rs77132938 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581234 | AAGTCCAGATGGCTA[C/T]GGTAAGCCAGAAAAG | 55213 |
rs77192529 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573236 | AAAGTATAATATATA[C/G]AGAAATGTATACACC | 55213 |
rs77239571 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564169 | AGGACAAGAACCTAT[C/T]AACCTGCATCCCCGG | 55213 |
rs77319818 | snp | A/C | 0.5 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535043 | CTGAAAGAAAATCCC[A/C]AAAAATTCACCTTAA | 55213 |
rs77512321 | snp | C/G | 0.0475351 | 0.146656 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560317 | AACATAGAAAGATCA[C/G]TTTTGTGATCAAAAG | 55213 |
rs77546321 | in-del | -/ACA | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574699 | TAAAAAAAAAAAAAA[-/ACA]TTAGAATTATATTAT | 55213 |
rs77627339 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49582873 | GAGTAAGAGGGGAGG[G/T]AGCAATAAACAGTGG | 55213 |
rs77783948 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49570567 | GTTTTGAGCCTGGGT[C/T]TCCCCCAAACCTAGA | 55213 |
rs77912906 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49582825 | AGGTCACCTATTTTT[C/T]CCCTATGAAGAAAGA | 55213 |
rs78166242 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49562208 | TCTGGAAAGAAACAT[C/T]TAAAGATCAAGAAAG | 55213 |
rs78476029 | snp | C/G | 0.0410537 | 0.137264 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534344 | TCTGAGCCCTTTACC[C/G]CAAATCTCTCACCCT | 55213 |
rs78584646 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49584909 | GGGAAACGTCACTTA[C/T]TTAGAGTTCACCGCA | 55213 |
rs78651944 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568151 | ATCTTTAAAAACAGA[A/G]GCACAAATGGAAGTT | 55213 |
rs78804466 | snp | C/T | 0.5 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49547692 | TATAATACCTCTGTT[C/T]TGATGCCCTTCTGAA | 55213 |
rs78845692 | snp | A/C | 0.5 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49558694 | GGTGAAACTCTGTCT[A/C]CAAAAAAAAAAAAAA | 55213 |
rs78988076 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538012 | AAACATTGGAAGCAG[A/G]TAGTCTCCATCTTCC | 55213 |
rs79016803 | snp | A/C | 0.0341408 | 0.126114 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49584123 | GCCAAGTTCTTGCTG[A/C]AGCATACGGGCACGC | 55213 |
rs79035778 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564166 | AAAAGGACAAGAACC[A/C/T]ATCAACCTGCATCCC | 55213 |
rs79137605 | snp | A/G | 0.0402882 | 0.136092 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533252 | AAGAGTATACTATAC[A/G]TGTCATTATTTTCCT | 55213 |
rs79540907 | snp | C/T | 0.242201 | 0.249878 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49585850 | CGAGGCACGGGCTCC[C/T]GCTCTGCTCCCCGAG | 55213 |
rs79566523 | snp | A/G | 0.0948562 | 0.196037 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548722 | ATATTGTATGCTTCC[A/G]CTTATATGAACTCTC | 55213 |
rs79665230 | snp | A/C | 0.5 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548390 | TGAGACTCCGTCTCA[A/C]AAAAAAAAAAAAAAA | 55213 |
rs79901078 | snp | A/C | 0 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49558698 | AAACTCTGTCTCCAA[A/C]AAAAAAAAAAAAAAA | 55213 |
rs80006341 | in-del | -/ACA | 0.444133 | 0.157519 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574929 | GAAATTCTGATACAT[-/ACA]ACAACAGGGATGAAC | 55213 |
rs80069456 | snp | A/G | 0.444533 | 0.157025 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569434 | CAAAAAAAAAAGGCC[A/G]GGCACGGTAGCTCAC | 55213 |
rs80145613 | snp | A/C | 0.0995161 | 0.199636 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554349 | TAACCTAAAAATTAA[A/C]CTTATTTTTAAAAAT | 55213 |
rs80305740 | snp | A/C | 0.5 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548389 | GTGAGACTCCGTCTC[A/C]AAAAAAAAAAAAAAA | 55213 |
rs80319630 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569159 | ACTCACATTTTAAGA[G/T]CCCACTGTCAGCCTT | 55213 |
rs111231984 | snp | C/T | 0.5 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49577570 | CCACCAATAGGGTAT[C/T]CTACCTTTAGATCTG | 55213 |
rs111292170 | snp | G/T | 0.0240643 | 0.107019 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49555127 | CATTCAAGATATAGG[G/T]AGGTAGTTCTACAAG | 55213 |
rs111297270 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49562163 | ATCTCAAATAGAAGA[C/T]GCTGAATCCATGAAA | 55213 |
rs111314871 | snp | C/T | 0.5 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49582933 | TGTAATCCCAACATT[C/T]TGGGAGGCCAAGGCG | 55213 |
rs111377946 | snp | C/T | 0 | 0 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49545125 | TACATTAGAAATGTA[C/T]ATTTTTAAAGAAAAA | 55213 |
rs111411444 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564869 | GCACTCCAGCCTGGG[C/T]GACAGAGAGAGACTC | 55213 |
rs111489218 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565627 | CGCCTCTGCCCAGCC[C/G]CGACCCCGTCTGGGA | 55213 |
rs111490732 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49572178 | CAAAAAATACAGAAA[C/T]TATCCAGGAGTAGTG | 55213 |
rs111520324 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49587085 | TCACACTGCCCAGAA[A/G]TAGACTGCGCATTTC | 55213 |
rs111570905 | in-del | -/AA | 0 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569719 | CTCAAAAAAAAAAAA[-/AA]GAAAGAAAGAAAGAA | 55213 |
rs111625052 | snp | G/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583692 | GCTGGGACTACAGGC[G/T]CACACCACCACGCCC | 55213 |
rs111666657 | snp | A/C | 0.5 | 0 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49545283 | AAGGGGTCAGCATAC[A/C]CAACTCAAGGAGGTG | 55213 |
rs111672228 | snp | A/G | 0.0573587 | 0.15934 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554592 | CAGGAGGTGAGCAGC[A/G]GGCAAGGGAGTATTA | 55213 |
rs111712004 | snp | A/C/G | 0.0244806 | 0.108077 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546721 | CACAATAGGGCTTAC[A/C/G]CTTCTTTGAGAATCT | 55213 |
rs111749191 | snp | C/T | 0.5 | 0 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49545628 | TGTGTTTTATATGTA[C/T]GAAAGAAGAAAAGAA | 55213 |
rs111759841 | snp | A/G | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533243 | TAGGAAGGCAAGAGT[A/G]TACTATACATGTCAT | 55213 |
rs111810875 | in-del | -/A | 0 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551155 | GGGGAAGGGGGAAGC[-/A]GGGAGGGAGAAGGAG | 55213 |
rs111929173 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49587126 | TGAATTGTCTATTGC[C/T]GTCTTCTCCCTTAGA | 55213 |
rs111986875 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49577381 | AAAAACAACAGGAAA[C/T]GGAGAGAAATGGTAC | 55213 |
rs112026939 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49585702 | GCTCTTCGGGCCCTA[C/G]AACCCGACTTCTTTA | 55213 |
rs112072299 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565600 | GCCGCCCATCGTCTG[A/G]GATGTGAGGAGCGCC | 55213 |
rs112100917 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538594 | TGGTGGCACACATCC[A/G]TAGTCCCAGTTCCTG | 55213 |
rs112190826 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49587044 | CTTCCCTGATTTCCA[A/G]AATACTATATATATT | 55213 |
rs112210859 | snp | C/T | 0.5 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565875 | GTTGCTGTGTCTGTG[C/T]AGAAAGAAGTAGACA | 55213 |
rs112268668 | in-del | -/A/AA | 0.563077 | 0.19339 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49575435 | ATAAATTGTTCTACC[-/A/AA]AAAAAAAAAAAAAAT | 55213 |
rs112269888 | snp | A/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564883 | GCGACAGAGAGAGAC[A/T]CCGTCTCAAAAAAAA | 55213 |
rs112271537 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49570385 | TTTCTCCAAAGACTT[A/G]TCATTTAAGAGTCAA | 55213 |
rs112275039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574563 | GCTTTAGATTCATAA[C/T]GTAGAGTGGCAGAAT | 55213 |
rs112275942 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49587587 | TCAGGGAGAAACTTC[A/G]TGAGAAGGTCAGTTG | 55213 |
rs112303323 | snp | C/T | 0.5 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568946 | AATAAAAAATAATGA[C/T]CAGAATAATTGCAAC | 55213 |
rs112387346 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571256 | GAGGCTGAGGCAGGA[G/T]AATCGCTTGAACCTG | 55213 |
rs112388488 | in-del | -/TAAA | 0.5 | 0 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49582488 | GCAAAATTCTGTCTC[-/TAAA]TAAATAAATAAATAA | 55213 |
rs112420555 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559458 | TCAGGAGATCGAGAC[C/T]ATCCTGGCTAACACG | 55213 |
rs112431182 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49537327 | TTTGTTCTCAAAATG[A/T]ACTTAAACATTCTAC | 55213 |
rs112443382 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586375 | ACTCCCAGTTGGCGC[C/T]GCAGGATAAAATCCA | 55213 |
rs112448304 | snp | A/G | 0.5 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564534 | GAGGTTGAGTGGGCC[A/G]AGATCATGCCACTGC | 55213 |
rs112464061 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571977 | AATTAATGAGTATTT[C/T]ATCTGTGATAAAATC | 55213 |
rs112527579 | in-del | -/AGT | 0.429087 | 0.174436 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559361 | AACTCAAAGAAACAG[-/AGT]AGAAAGTTGTTGGCT | 55213 |
rs112544316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49582625 | GGAATCCAGATGCTG[A/G]AGACATACTCATTCT | 55213 |
rs112553661 | in-del | -/AGAG | 0.43221 | 0.171171 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563334 | TCCTGCCTGGGTGAC[-/AGAG]AGAGAGAGACCCTGC | 55213 |
rs112555229 | snp | A/G | 0.5 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548300 | AGGAGGCTAAGGCAG[A/G]AGAACTTGAACCTGG | 55213 |
rs112638612 | snp | A/G | 0.5 | 0 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546035 | TAGAAAACCTCTCAA[A/G]AGTCAGGCTTCCCCT | 55213 |
rs112654999 | snp | C/T | 0.5 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49580041 | CCTCAGCCATGTGCT[C/T]GAAAAGCAAACGAAC | 55213 |
rs112682434 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49550581 | GTCCTTTCAAGAGCA[-/G]ATTTATTTAAAAGTT | 55213 |
rs112718824 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49587262 | GTTGAGTGAATTTAC[C/T]AGAAGAGGCCTGTTT | 55213 |
rs112800574 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534561 | AAAGAATTTCCTGCA[C/T]GATTATCACATAATC | 55213 |
rs112802948 | snp | A/G | 0.5 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565855 | AAAGATAGAGAAATC[A/G]GATTGTTGCTGTGTC | 55213 |
rs112813796 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586215 | CCATAGAGGTTAGAC[A/G]GGACCTAAGAGGGCA | 55213 |
rs112815634 | in-del | -/TGC | 0.5 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49585244 | GCACATTAGCTGAGG[-/TGC]TGCTGGCGGGGCCGG | 55213 |
rs112893956 | snp | A/C | 0.0298908 | 0.118541 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49545171 | ATGATAATATAATAA[A/C]CCCCTCTCAAAACGA | 55213 |
rs112904671 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534715 | GGTAATGAAGAGATA[C/T]GGTCAACCTAAAGTG | 55213 |
rs112927684 | snp | G/T | 0.5 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583997 | ACAGAAGGGATATCA[G/T]CATCATAATAAAGGT | 55213 |
rs112963066 | in-del | -/A | 0.429987 | 0.173507 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49556583 | TCCTCCAACATTAGG[-/A]AAATGTCTAAGCCCC | 55213 |
rs112997157 | snp | C/G | 0.5 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554594 | GGAGGTGAGCAGCGG[C/G]CAAGGGAGTATTACT | 55213 |
rs113012683 | in-del | -/G | 0.110519 | 0.207473 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49580494 | TCAAGAGGCTGAGGT[-/G]GGAGGATCACCTGAG | 55213 |
rs113089751 | snp | A/G | 1.74515e-05 | 0.00295389 | synonymous-codon, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49555668 | GTTATAACCCCAAGC[A/G]AACACCTACAAGAGA | 55213 |
rs113144998 | snp | A/G | 0.5 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49555097 | CTGCTTTTGCAAGTT[A/G]CTTCCTCCTGTGAAC | 55213 |
rs113172923 | snp | C/G | 0.093417 | 0.194889 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538956 | AGTGGTACAACTTCT[C/G]CCTCCCAGATTCAAG | 55213 |
rs113249462 | snp | A/T | 0.5 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551958 | CTACTGAATTTTTCC[A/T]TTTTTTTTTTTTTTT | 55213 |
rs113250462 | snp | C/T | 0.5 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541201 | CCTATATTTACTTTA[C/T]ACAATTTCTTCAATA | 55213 |
rs113365697 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574173 | GCCCAGTCTGGAGTA[C/T]ACTGGCACCATCTTG | 55213 |
rs113367350 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586946 | AAATCCAGGTCAAAT[A/G]CCGCCTACTCTTGTC | 55213 |
rs113389663 | snp | A/G | 0.5 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49570868 | GGACTGAGGCTCAAA[A/G]GTGAAATGACGCCAA | 55213 |
rs113426639 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569460 | CTCACTCCTGTAATC[A/C]CAGCACTTTGGGAGA | 55213 |
rs113461026 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548157 | AGCACTTTGGGAGGC[C/T]GAGGCGGGCGGATCA | 55213 |
rs113516369 | snp | A/G | 0.5 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49555788 | TACTTAAGATGTGCT[A/G]AACGGTTCTATATGC | 55213 |
rs113516992 | snp | A/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574687 | ATGGTGATTCCTTAA[A/T]AAAAAAAAAAAACAT | 55213 |
rs113616190 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564620 | AAAAATGCCGGGCGC[A/G]GTGGCTCACGCCTGT | 55213 |
rs113691744 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586534 | TTAAAAAAGTCCTAC[C/T]GTCCCTCATCTCTTG | 55213 |
rs113720447 | snp | A/G | 0.5 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49576793 | CAATATTAATGTGTT[A/G]CAGCCTGAATTACCA | 55213 |
rs113721606 | snp | A/C/G | 0.0248705 | 0.10889 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49547852 | GGAGTGCAGTGGTGC[A/C/G]ACCACAGTTCACTGC | 55213 |
rs113743888 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559452 | ACGAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT | 55213 |
rs113746640 | snp | C/G | 0 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559639 | CCAGCCTGGGCGACA[C/G]AGCGAGACTCCATCT | 55213 |
rs113783746 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586953 | GGTCAAATGCCGCCT[A/G]CTCTTGTCTTCCCAG | 55213 |
rs113786978 | snp | C/G | 0.5 | 0 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49570848 | AAACCATTTCTGACA[C/G]ATGAGGACTGAGGCT | 55213 |
rs113806809 | snp | A/C | 0.0644693 | 0.167566 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539082 | ACCATGTTGGCCAGG[A/C]TGGTCTCAAACTCCT | 55213 |
rs113812823 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49577390 | AGGAAATGGAGAGAA[A/G]TGGTACAGGAAAACT | 55213 |
rs113825223 | in-del | -/A | 0.5 | 0 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546145 | TACCCCCACCCATCC[-/A]AAAAAAAACCCACTT | 55213 |
rs113900021 | snp | A/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49547953 | CCACCACTCCTGGTT[A/T]TTTTTTGTAGAGATG | 55213 |
rs113939381 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49575179 | CACTAATCATCAGAG[A/G]AATCCAAATCAAAAC | 55213 |
rs113965649 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49572502 | GTTCAACTAAATTTC[A/G]TTTAAATAATCATTC | 55213 |
rs113988609 | snp | A/C | 0.5 | 0 | downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49531873 | GTTCACCTCTGTGCA[A/C]CATGTGTCAGAATTT | 55213 |
rs113993240 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49550039 | CCGTCACCCAGGCTA[C/G]AGCGCAGTGGCATGA | 55213 |
rs114006752 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49536305 | AAAGGAAGCCCTGAA[C/T]GCATGTGGTGAGGGA | 55213 |
rs114126793 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49556936 | TGGCACTTCTCAAAT[A/G]CATCACATTCCCTTG | 55213 |
rs114182719 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49579309 | TCCACGTCTCTCTTC[C/T]GCAAACACACAGTAC | 55213 |
rs114329730 | snp | G/T | 0.0283406 | 0.115616 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569766 | AAAATTATTAGCCAG[G/T]CATGGTGGCGCATGC | 55213 |
rs114674249 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573040 | GCTATGGTTTGTCCA[A/G]ATTATAAGCACCCCC | 55213 |
rs114815509 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49561786 | AAGGTAGCTAATTCT[A/C]CCAGTTACTAAAACC | 55213 |
rs114913654 | snp | G/T | 0.0225045 | 0.103662 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553388 | TCGTTAGCAAATAGG[G/T]GAGCTCTGATGAGGC | 55213 |
rs115058632 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568497 | TTCTATTGAAGTAGT[A/G]GCCATATATAAAATC | 55213 |
rs115125295 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49537147 | GTGCCTCGGCATCAC[A/G]GCTCCCCACAAGACA | 55213 |
rs115247033 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573052 | CCAAATTATAAGCAC[C/T]CCCCAAGGAAGCATC | 55213 |
rs115258698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49537502 | CCCAGACCAACTTCA[A/G]AATTAGATTCCTGGG | 55213 |
rs115332381 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557730 | TTCAAGACCAGCCTG[A/G]GCAACATAGCCAGAT | 55213 |
rs115635287 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569843 | ACCCAGGAAGTCAAG[A/G]CTGCAGTTGAGCCGA | 55213 |
rs115648900 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568267 | GGCATTCCATTACAT[C/T]GATTTAGCAATTTAC | 55213 |
rs115695806 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568407 | TTTCTAAAATAAATT[C/T]CTAAAAATGAAAATT | 55213 |
rs115703289 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49536734 | AAGGGTCTAATACAG[C/T]CTTCTTGGTATTAGA | 55213 |
rs115829930 | snp | C/T | 0.0391387 | 0.134304 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49587091 | TGCCCAGAAATAGAC[C/T]GCGCATTTCCTGTAA | 55213 |
rs115831213 | snp | A/C | 0.0240643 | 0.107019 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574774 | AGCAGAGACTTGAAC[A/C]GATAGTTGTATACCA | 55213 |
rs115834972 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49584099 | CCCAGCTCCCGTATA[C/T]TAGGTGGAGCCAAGT | 55213 |
rs115928576 | snp | C/T | 0.0130921 | 0.0798413 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49534013 | AGATGTGGAAAAAAA[C/T]AACCTGATGGTCTTT | 55213 |
rs115937403 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564966 | CAGAACAAAGACCAG[C/T]GAGCTATTAAGGAAT | 55213 |
rs116109410 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535362 | TATTTATTAAATCGA[C/T]TAGGCACCTGGAATG | 55213 |
rs116118979 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542954 | TTTTAAAGTGAGATA[C/T]GGCACAAAGAGAAAA | 55213 |
rs116214754 | snp | C/T | 0.0685596 | 0.171987 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554530 | CCCCAGCTCATGAGC[C/T]GCAGGCCGGTACCAG | 55213 |
rs116226094 | snp | C/T | 0.126219 | 0.217206 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574787 | ACAGATAGTTGTATA[C/T]CAACGGTCAAAGCAG | 55213 |
rs116227107 | snp | A/T | 0.0225045 | 0.103662 | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49549189 | TTCTAAACGCAACTA[A/T]ACTGTACCCTTTACA | 55213 |
rs116344821 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49578073 | TATTGTATGCTAATG[C/T]GAACAAAATCCAGTT | 55213 |
rs116376722 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49558137 | TGTCTGTGTGGGTTT[C/T]CTCTGGGTACTCTGA | 55213 |
rs116523488 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552488 | ACTCCATGACTTACT[A/G]GTTAGATAGTCTGGG | 55213 |
rs116591037 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49562229 | ATCAAGAAAGAACAC[C/T]TGGAAATAAAACAAT | 55213 |
rs116740525 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581737 | GAGACAGAGTGTCAC[A/G]GAGATCTGGGGACTT | 55213 |
rs116752986 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49545601 | CTTGTACAAATTCCC[A/G]GAATGCTTTCTTGTG | 55213 |
rs117100320 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49572660 | ATACAAAAATTACCC[C/T]GGGTGTGGTGGCGCA | 55213 |
rs117255675 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552372 | CCCATCTAAACAAAT[C/G]AGATACTTCCAACAC | 55213 |
rs117308143 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49531617 | GACCTCTTCCTAACA[C/T]GCCAGGGATGAATAT | 55213 |
rs117345716 | snp | C/T | 0.000149228 | 0.00863664 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49567215 | AAGACACACGCCTTC[C/T]GAATAGACGCGATCT | 55213 |
rs117668059 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49580938 | CACAACAGTGTGGCT[A/G]GTCAGATGCTGTGGA | 55213 |
rs117687337 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49550376 | GTCACGGACTCTGAA[A/C]GTTCCAATCCAAAAG | 55213 |
rs117726715 | snp | C/G | 0.0908922 | 0.192833 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49567939 | TGAGGACAAGTAAAA[C/G]ATTTGACAGGGGAGT | 55213 |
rs117872701 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566460 | TTCCAGAGTTAGCCC[A/G]AAGTGTTTAACTTTC | 55213 |
rs117881124 | snp | C/T | 0.0267878 | 0.112589 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586694 | CTGTATCTGAAATGT[C/T]CTGAATCACCACCTC | 55213 |
rs117959005 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560236 | ATGGACAGAGTAAAG[C/G]AGAGAGAGATGGGTG | 55213 |
rs118167683 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563527 | AATTAGCCAGGCATG[C/G]TAGCATATGCCTCTA | 55213 |
rs137879162 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560437 | ATAAGAAAGCTCGAT[A/G]TTAATGTTTACCATT | 55213 |
rs138021762 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49575102 | GTTTAATGGGTACAG[A/C]GTTTCACTTTGGGGT | 55213 |
rs138081615 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546233 | TTTGCTCCTGGCAAC[A/G]AGTATAGTACATCCT | 55213 |
rs138185136 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554114 | TGCTATACAGGGGAG[C/T]GGGAAGCAGGCTGAA | 55213 |
rs138203444 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49543658 | ACAGTTACTAATAAA[C/T]GCATAGGTCCCTCAC | 55213 |
rs138304379 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49558490 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 55213 |
rs138308390 | snp | G/T | 0.0106835 | 0.0723022 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49566688 | CTTTCCACATAAGCC[G/T]TCTAGCTTTTTGGGT | 55213 |
rs138373313 | in-del | -/AC | 0.268995 | 0.249277 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574699 | TAAAAAAAAAAAAAA[-/AC]ATTAGAATTATATTA | 55213 |
rs138534043 | in-del | -/ATAAAG | 0.482008 | 0.0931261 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49532196 | GTGTATTTAAAAAAA[-/ATAAAG]ATAATCAAATGCTTT | 55213 |
rs138657706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542897 | TGGATTTTCTTATGT[A/G]TAACACAGTTGTATC | 55213 |
rs138697375 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49536425 | CAAGTTAGACAAACG[C/T]CCTTCCGACTTGACC | 55213 |
rs138715361 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581348 | ACAAGGAGCACTGGA[C/T]AAGCAGAAAGGCAGA | 55213 |
rs138779579 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551575 | TGCCAAATCATCATC[-/A]GGGGTGGACTGACAT | 55213 |
rs138797685 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569510 | TGAGGTCAAGAGTTC[A/G]TGACCAGCCTGGCAA | 55213 |
rs138869400 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49575862 | ATACCCATGTAACAA[A/G]CCTGCATATGTACTC | 55213 |
rs138937659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49572611 | AGTTTGAGACCAGAC[C/T]GGCCAACATGGCAAA | 55213 |
rs138940509 | snp | C/T | 0.000264787 | 0.0115032 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49567208 | GGTGCCGAAGACACA[C/T]GCCTTCCGAATAGAC | 55213 |
rs138992042 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564456 | CGGGGCGTGGTGGCA[C/T]GCGTCTGTGGTCTCA | 55213 |
rs138997790 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49582948 | TTGGGAGGCCAAGGC[A/G]GGAGGACTGCTTGAG | 55213 |
rs139163191 | snp | A/G | 0.00917268 | 0.0670985 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49555496 | GGTAGAAAGGGAAAT[A/G]GGAGTGGAGACACCT | 55213 |
rs139202166 | in-del | -/TAATA | 0.0130921 | 0.0798413 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49532268 | AATGACTTAGTAATC[-/TAATA]TGAGAAGTGGTCCTT | 55213 |
rs139231771 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557576 | ACAGAACACTGTCAC[A/C]CATCTGAGCTATAGT | 55213 |
rs139307825 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569982 | CTCTTACAAAACAGA[A/T]GGAGAAAGGAGTCAT | 55213 |
rs139376833 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554681 | GAACCCCATTGTGAA[C/G]TGCACAACAAGGCAT | 55213 |
rs139425954 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49544959 | GACCGTGATGGATAA[C/T]TCCACTTGTTTTTTT | 55213 |
rs139445321 | snp | C/T | 0.000187342 | 0.00967656 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49552192 | CCTGGTTCACACACA[C/T]GCTGTGCAAAGCTGC | 55213 |
rs139454193 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49545543 | TTGCTGTTGTGGTTA[C/T]ATGTTAAGTAGAACT | 55213 |
rs139554128 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49576337 | TTTTACACTATATAC[A/C]TTTTACCCCAATTTT | 55213 |
rs139582953 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538307 | TATGGATTTTAATTT[C/T]GTACTCCAGAACTTC | 55213 |
rs139639100 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539090 | GGCCAGGCTGGTCTC[A/G]AACTCCTGATCTCAA | 55213 |
rs139660032 | snp | G/T | 1.70035e-05 | 0.00291572 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49541004 | TCGCCAAATCCAGAA[G/T]ACCTAAAAGTAAAAT | 55213 |
rs139688718 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49537765 | ATTTATTCAGGTCTG[C/T]ACCAAAGGAGTATCT | 55213 |
rs139714193 | snp | C/G | 0.00331111 | 0.0405536 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49555524 | CCTCACCTCGCCATT[C/G]TCCAGAACAGCCATG | 55213 |
rs139725749 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533761 | GCTGTCAGAAGATTG[C/T]TGATACGTGGCCCAG | 55213 |
rs139845222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49561353 | TCCTCTTCCAGGTGA[C/T]ATGTGGCTCACAAGA | 55213 |
rs139845615 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49578006 | TACGAAAAAAATTTA[C/T]TTATAGTTAATGAGC | 55213 |
rs139878215 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539328 | AGGAAGTTTTTATCA[C/T]GTTTATACTTAATAT | 55213 |
rs139918478 | snp | C/T | 0.0955749 | 0.196603 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559404 | GCTCACGCCTGTAAT[C/T]CCAGCACTTTTGGAG | 55213 |
rs140027458 | in-del | -/AAAGTGAAAGATGAT | 0.487432 | 0.0782705 | utr-variant-3-prime, cds-indel, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533071 | AACAGAGGAAAACCA[-/AAAGTGAAAGATGAT]AAAGTTTCACATAAG | 55213 |
rs140118443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49582351 | AATTAGCTGGGCATA[A/G]TGGTGGGTGCCTGTA | 55213 |
rs140188843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571452 | TTTATTCCTGCACTT[C/T]TGCATCAACCATTGA | 55213 |
rs140419890 | snp | A/G | 4.94205e-05 | 0.0049707 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49560026 | AGCAATGCCTTGGTT[A/G]GTCGTCCCATTCCCA | 55213 |
rs140432497 | in-del | -/CA | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534515 | ACACACACGCGCGCG[-/CA]CACACACACACACGC | 55213 |
rs140483693 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563230 | CATGGTGAGACCTCA[C/T]CTCTACAAAAAAATT | 55213 |
rs140538533 | in-del | -/TCT | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538819 | GAGTCTTTCTTTTTG[-/TCT]TCTTTCTATTCTCTA | 55213 |
rs140636532 | in-del | -/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49576843 | ATGACTTTTTTTTTT[-/T]AACTGTATAAAGATA | 55213 |
rs140643932 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571333 | CCTGGGGAAGAAGAG[A/C]GAAACCCCATCTCAA | 55213 |
rs140664292 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534989 | CGGTGAGCCGAGATC[A/G]CACCACTGCACTCTA | 55213 |
rs140712130 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538994 | CCTGCCTCAGCCTCC[C/T]GAATAGCTGGGATTA | 55213 |
rs140806240 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581237 | TCCAGATGGCTATGG[C/T]AAGCCAGAAAAGAAG | 55213 |
rs140833440 | snp | G/T | 0.0295035 | 0.117819 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542183 | TGCGCTTCTGCACTC[G/T]AGCCTGGCAACAAGA | 55213 |
rs140910819 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586905 | ACAGCCTCCAAAGTA[C/T]ACATCAGTTTCCTAC | 55213 |
rs141095690 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49567622 | TTAGACCTCTAAAAA[C/T]AGCCAAAGCAGCAGG | 55213 |
rs141154020 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49579573 | AGCTTGCAGTGAACC[A/G]AGATGGTGCCACTGC | 55213 |
rs141193665 | snp | C/G | 0.0452528 | 0.143452 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565187 | ACCTGACTGGTTTTC[C/G]TATTTTTTTGGTGGA | 55213 |
rs141359633 | in-del | -/AAGAT | 0.429987 | 0.173507 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552839 | TAGAAGCTAGTTTAG[-/AAGAT]AAGTAGGTGGGCTTG | 55213 |
rs141367582 | snp | G/T | 0.00014834 | 0.00861092 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49566741 | CAGTTCCTAGACAGT[G/T]ACTATAGTTCAGTCC | 55213 |
rs141396616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535591 | GAAGGGGCCCACACA[A/G]ACATGGAGAGACCCC | 55213 |
rs141490629 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553408 | TCTGATGAGGCTCTA[A/C]ACTAAGGAGTGATAG | 55213 |
rs141530252 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49544677 | ATCAGTACTCATTTT[G/T]TGGAATAACAAAGAA | 55213 |
rs141536179 | snp | A/G | 1.65051e-05 | 0.00287267 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49534250 | AAAACTTAAAGCAGA[A/G]TTCTTCTAAATCCTG | 55213 |
rs141601082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49582206 | AAGTGCAACAGAAGC[A/G]CCGGGCGCAGTGGCT | 55213 |
rs141643071 | in-del | -/TTA | 0.279991 | 0.248195 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49547951 | CACCACCACTCCTGG[-/TTA]TTTTTTGTAGAGATG | 55213 |
rs141645569 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49551449 | GTTAGTGCTAGAGTA[C/T]GTGCGTAACCGCAGA | 55213 |
rs141776877 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49537445 | AAGAAGAAAAAAACG[C/T]TGGCCACCAAGCCTT | 55213 |
rs141883335 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573209 | TATGTCCTGTATGAT[C/T]ACAATTTTTCTAAAG | 55213 |
rs141927350 | in-del | -/AGAA | 0.0429648 | 0.14013 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560307 | ACTTGGTAATAACAT[-/AGAA]AGATCAGTTTTGTGA | 55213 |
rs141981076 | in-del | -/AAACAAAC | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49544474 | AACTCTGTCTCAAAG[-/AAACAAAC]AAACAAACAAACAAA | 55213 |
rs141981677 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49572252 | GGATCGTTTGAACCT[A/G]GGAGGTGGAGGTTGC | 55213 |
rs141996607 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49576498 | TTTTAATCATGTCTT[A/G]AGAATATAAGTTCAG | 55213 |
rs142026884 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581458 | CCTCAGGGGTGATGA[A/G]TCCTACTATGGACAT | 55213 |
rs142035882 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49555297 | AATACAACTTAGACA[C/T]ATAGAATCTTTACTT | 55213 |
rs142073389 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541306 | TACTTCACTACTAGA[A/C]AATTAAAATAAGCCC | 55213 |
rs142091390 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49575866 | CCATGTAACAAACCT[A/G]CATATGTACTCCCTG | 55213 |
rs142200131 | snp | C/G | 0.000153988 | 0.00877328 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49559981 | TTCCACCACTTGCTT[C/G]ATCAAGAGATTGGTA | 55213 |
rs142239846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49584076 | AAGGAGGGTACTGTT[C/T]CAGACTTCCCAGCTC | 55213 |
rs142332312 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534892 | TACAAAAATTAGCCG[A/G]GCGTGGTGGTGGATG | 55213 |
rs142373322 | snp | C/G | 6.60327e-05 | 0.00574561 | missense, downstream-variant-500B, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549502 | GGAGTGGCAAAGCAG[C/G]CAAACACGTCGTCGG | 55213 |
rs142436789 | in-del | -/GGA | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568652 | AATAATCAGGCCGGG[-/GGA]GGGGGGTGGCTCACA | 55213 |
rs142548832 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574206 | TCACTGCAACCTCCA[C/T]CTCCCCAGTTCAAGC | 55213 |
rs142774117 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546278 | CCTCCTCAAAGGGGT[A/G]AATTCACCATGTGAC | 55213 |
rs142780106 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49572978 | ACAGTCAAGTACCTT[A/G]GTAAGTACCCTGAGC | 55213 |
rs142805271 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49567465 | TCACTCACTTTCCCC[C/T]AGCCATGTGTGCAAT | 55213 |
rs142811014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49536438 | CGCCCTTCCGACTTG[A/G]CCTCTCTTTAGTATT | 55213 |
rs142900016 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49544249 | CTGAGGCGGGCAGAT[C/T]ACCTGAGATCGGGAG | 55213 |
rs142944522 | snp | C/T | 0.00874735 | 0.0655527 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49532998 | ATCTTTTCAGGAACA[C/T]CATAATTTTGGTGCT | 55213 |
rs142953686 | snp | A/G | 4.94222e-05 | 0.00497078 | synonymous-codon, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49551394 | AGTTCCCAGCTGCCC[A/G]TATGTGTTAGCTCCC | 55213 |
rs143011959 | in-del | -/GGGA | 0.258843 | 0.249844 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568651 | AAATAATCAGGCCGG[-/GGGA]AGGGGGGTGGCTCAC | 55213 |
rs143070387 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49541707 | CGGCAGGTCGACTGT[A/G]TCTGTGTAGAGGTAC | 55213 |
rs143078084 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49536243 | AACAATCTAAATCTG[G/T]GTTGTGTAAGTAACT | 55213 |
rs143145454 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49545787 | TCAAAGACCTCGGCT[C/T]CCAAGCCTGGGATGA | 55213 |
rs143270235 | snp | C/G | 0.0217236 | 0.101931 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49575850 | GCATCACACGCTATA[C/G]CCATGTAACAAACCT | 55213 |
rs143298413 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554733 | AGAATCTAACTCATG[C/T]TTGATGATCTGAGGT | 55213 |
rs143362251 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557797 | AATGAATTCTACTGC[C/T]ATCAAAAGTGTAATC | 55213 |
rs143444999 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568814 | TGTGCCTGCAGTCCC[A/G]GCTACTCAGGAGGCT | 55213 |
rs143587451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49580052 | TGCTCGAAAAGCAAA[C/T]GAACCAAGTGGCAAT | 55213 |
rs143686770 | snp | A/G | 1.65414e-05 | 0.00287583 | missense, utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549598 | ACGTGCCCACCCTGC[A/G]TCTTGGCTGCAGACG | 55213 |
rs143715960 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569148 | CTTCACCTCTCACTC[A/G]CATTTTAAGAGCCCA | 55213 |
rs143796902 | in-del | -/CGCCGGGCC | 0.242201 | 0.249878 | utr-variant-5-prime, cds-indel, upstream-variant-2KB, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49585566 | GGAGGAGCGCCAGGG[-/CGCCGGGCC]CGCCGGGTCACGTGG | 55213 |
rs143899297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554784 | CCATGCCCCCAACAC[C/T]GCCATCTGTGGAAAA | 55213 |
rs143970072 | snp | C/T | 0.000149225 | 0.00863657 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49544758 | TTCAAAACAGCTTTA[C/T]GGACATGAATATATT | 55213 |
rs144004736 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554397 | ATGGAGGATATTCAA[C/T]GGCCATCCCAAGGAA | 55213 |
rs144034572 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559378 | TAGAAAGTTGTTGGC[C/T]GGGCACGGTGGCTCA | 55213 |
rs144109204 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49555792 | TAAGATGTGCTAAAC[A/G]GTTCTATATGCTTTA | 55213 |
rs144274579 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539111 | CTGATCTCAAGTGGC[C/T]CACCTTGGCCTCCCA | 55213 |
rs144281624 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49582667 | TCTCTCTCCCCGCTG[A/G]GTCTCCATTTTACAT | 55213 |
rs144369161 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581806 | GCTGAGACACCAAAC[A/G]AGGGAAGGGTGGAGA | 55213 |
rs144405400 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571350 | AAACCCCATCTCAAA[A/G]AAAAAAGAAGTATCC | 55213 |
rs144422503 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538338 | ATTCATGTACTCACT[A/G]TATCTTGTAGCATTC | 55213 |
rs144427397 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49558571 | TGGTGGCAGGCGCCT[A/G]TAATCCCAGCTACTC | 55213 |
rs144545635 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573003 | CTGAGCAAGGTAGCC[C/G]AACTCTCTTCCTTCC | 55213 |
rs144578675 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563135 | CCAGGCATAGTGGCT[A/C]ACACCTGTAATCCCA | 55213 |
rs144640629 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566434 | CTAATTTGCAAGACA[A/T]CCTATAGCTTTTCCA | 55213 |
rs144641365 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568248 | TTCTTTCCAATGGTA[C/T]TATGGCATTCCATTA | 55213 |
rs144736337 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538193 | AGATGGCAGTCTCAC[G/T]ATGTTGTCCAGGCTG | 55213 |
rs144805684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548693 | AAGTAAAAGAAGCCA[A/G]ACACATGGGTCACAT | 55213 |
rs144921299 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583074 | CCCAGCTACTTGGGA[A/G]TGGGGAGGATCACTT | 55213 |
rs144922510 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49578655 | ATAGGAAATAATTAT[A/G]TGCAAACTAGTGACA | 55213 |
rs144952015 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548232 | CTGTCTCTACTAAAA[A/G]TATAAAAAAATTAGC | 55213 |
rs144982453 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49545655 | AGAAGCAGAAAAGGG[A/C]TAATGGGGAAATTTT | 55213 |
rs145016785 | snp | C/G | 0.0402882 | 0.136092 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553108 | AATCACTTGAACCTG[C/G]GAGGCAGAGGTTGCA | 55213 |
rs145048168 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49550145 | CACCATACCCGGCTA[A/G]GTTTTGTATTTTTTA | 55213 |
rs145096562 | snp | A/G | 0.000315151 | 0.012549 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49566766 | CAGTCCAAATACAAA[A/G]ACCTAGAAAATAGAT | 55213 |
rs145183342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49567895 | GATGTCTTGACAAAT[A/G]TGTGTGCAGGTGGAG | 55213 |
rs145228811 | snp | A/G | 0.000594157 | 0.0172257 | synonymous-codon, missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49559924 | CATACTTACCTCTCC[A/G]TCAGCTGCCAGAGCC | 55213 |
rs145260538 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539576 | GCGTGGAGAGGCCCA[A/G]AGAGGATTCTAACAT | 55213 |
rs145333325 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563398 | CCAGGCACAGTGGCT[C/T]ATGCTTATAATCCCA | 55213 |
rs145362282 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534335 | TTACTTCTCTCTGAG[A/C]CCTTTACCCCAAATC | 55213 |
rs145556185 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546130 | AGGAGTCTAGATTGC[C/T]ACCCCCACCCATCCA | 55213 |
rs145647493 | snp | A/G | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49545028 | GGTATTAAAGTAAGT[A/G]TCCTGCATCTATAAA | 55213 |
rs145673931 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49585331 | CCGAGCGAGGGAGGC[G/T]GGAGGTACAGGAGTA | 55213 |
rs145723396 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581544 | GAAATCTGAAGCTCA[A/C]GAAAGGTCTGGATTG | 55213 |
rs145735095 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49556392 | AGATGGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 55213 |
rs145752166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535318 | TGCCAAACTTTAATA[C/T]AGTCTGTCCCTTAGG | 55213 |
rs145769772 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574330 | CACCATGTTAGCCAG[A/G]CTGGTCTCAAACTCC | 55213 |
rs145811385 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583388 | TGTGCTTTTGTGTAT[A/G]TGTGTGTGTGTGTGT | 55213 |
rs145870790 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49540541 | TAAGTCTCGAAATAA[A/T]CACATATGCTGACAT | 55213 |
rs145971135 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49561239 | AATCCAAGTATTACA[G/T]TTAGGCTGCTGGTCA | 55213 |
rs146012288 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559383 | AGTTGTTGGCTGGGC[A/G]CGGTGGCTCACGCCT | 55213 |
rs146086129 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49572292 | AGATCATGCCACTGC[A/C]CTCCAGCCTAGGCGA | 55213 |
rs146092604 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49544285 | GACCAACCTGACCAA[C/T]ATGGAGAAACCCCAT | 55213 |
rs146135479 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539285 | GTGACAGACTCTGGG[G/T]AATCACACTTATTTG | 55213 |
rs146138087 | snp | A/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49541736 | ACTGGAGAAAGGCAC[A/G]ATACACTGGGTAAGA | 55213 |
rs146165279 | snp | A/G | 6.58946e-05 | 0.0057396 | synonymous-codon, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49551400 | CAGCTGCCCATATGT[A/G]TTAGCTCCCCAGGCA | 55213 |
rs146299784 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49576309 | TGTAATTAAAAATCA[C/T]TAAAATGGTAAATTT | 55213 |
rs146312408 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49543367 | TTGTCTAAGAAAGAA[C/T]CATGGATTTCATGGT | 55213 |
rs146380827 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573770 | TGTATTTTTAAAATA[C/T]AGTCCCAAATTTCTC | 55213 |
rs146480436 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49555821 | TACACACATTAACCT[A/G]TTTAACCTGCCTAGT | 55213 |
rs146521559 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552968 | GTGGGCAGATCACCA[A/G]GTCAGGAGATCGAGA | 55213 |
rs146599859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538549 | AACCCTGTCTCTACA[A/G]CAAATAAAAAATAAG | 55213 |
rs146639534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535432 | AGCTCTTATCACAAA[C/T]AGCTTGACTTTATTA | 55213 |
rs146720001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49584130 | TCTTGCTGCAGCATA[C/T]GGGCACGCTTTAAAA | 55213 |
rs146836805 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557279 | GGGACTATGGCAGTA[A/G]TCTAGGCAGGAAATG | 55213 |
rs146841476 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568061 | CTCAAAGGCCACCAC[C/T]GTTCCCAGTGATCTG | 55213 |
rs146955596 | snp | A/T | 0.000131859 | 0.00811862 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49541738 | TGGAGAAAGGCACGA[A/T]ACACTGGGTAAGAAA | 55213 |
rs147290766 | snp | C/G | 0.0252325 | 0.109451 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554657 | AGCATAAGATTCTCA[C/G]AGGAGCACGAACCCC | 55213 |
rs147327509 | snp | C/T | 0.000348048 | 0.0131872 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549612 | CGTCTTGGCTGCAGA[C/T]GTGTGGGCAGAGTGA | 55213 |
rs147353299 | in-del | -/AA | 0.000446019 | 0.0149268 | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49540869 | TTCTGTTTGTTGTTT[-/AA]GTTACCTCTGCATCA | 55213 |
rs147396015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49536769 | AAACTCTGTTTATGA[C/T]GTTATGTGGCAGAAC | 55213 |
rs147432000 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533104 | GTTTCACATAAGCCA[A/G]TGTGTGATGGATTTG | 55213 |
rs147472617 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569829 | AGAGGATTGCTTGAA[C/T]CCAGGAAGTCAAGGC | 55213 |
rs147591987 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49545671 | TAATGGGGAAATTTT[A/T]TTAAATTCCAGAGAT | 55213 |
rs147650879 | snp | C/T | 0.000412014 | 0.014347 | missense, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49559941 | CAGCTGCCAGAGCCA[C/T]TGAATGATGTGAGCC | 55213 |
rs147766283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541420 | CTGCACGTGTACCCC[A/G]GAACTTAAAAATAAA | 55213 |
rs147783614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574412 | GCGTGAGCCACCATG[C/T]TCGGCCAGTCCCAAA | 55213 |
rs147870894 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566435 | TAATTTGCAAGACAT[C/T]CTATAGCTTTTCCAG | 55213 |
rs148013171 | snp | C/T | 0.00159617 | 0.0282053 | downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49531463 | TATGGAGCACACAAC[C/T]TAGATCCCTTGCATA | 55213 |
rs148044318 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573193 | CTATGTTATAAAACA[A/G]TATGTCCTGTATGAT | 55213 |
rs148118639 | snp | C/G | 0.0640965 | 0.167152 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49556453 | TCTCGGCCTCCCAAA[C/G]TGCTGGGATTACAGG | 55213 |
rs148172878 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559687 | AGAAAGTTGTTGTCA[G/T]GGGCTGGGGGAGGAC | 55213 |
rs148226814 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564971 | CAAAGACCAGTGAGC[C/T]ATTAAGGAATAGGAT | 55213 |
rs148295247 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553137 | CAGTGAGCCAAGATC[A/G]TGCTACCGTACTCCA | 55213 |
rs148490155 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49561958 | AAATACAAAAATCAG[C/T]CAGGCATGGTAGCGC | 55213 |
rs148498959 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566924 | CAACCTCTGTGGACA[C/T]TGCTTACGTTTCAGA | 55213 |
rs148558091 | snp | C/T | 0.00023291 | 0.0107889 | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49549414 | AAACTGGTCAGTTGG[C/T]AGTACCATTCTTCCT | 55213 |
rs148567769 | in-del | -/G | 0.0298908 | 0.118541 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49545480 | CAACACCTACATGAA[-/G]GGAACAGTTTTATAA | 55213 |
rs148610712 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554829 | AACCAGTCCCTGGTG[C/T]CAAAAAGGTTGGGGA | 55213 |
rs148632653 | snp | C/T | 0.000198232 | 0.00995374 | synonymous-codon, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49544808 | CAGATCAGCAGTTTC[C/T]GGACTATCAAATTCT | 55213 |
rs148725728 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571040 | GCATCTGTCTTTAAA[C/T]TGTTACCAATATAAA | 55213 |
rs148812082 | snp | G/T | 0.0376037 | 0.131863 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568734 | AAGAGATCGAGACCA[G/T]CCTGACCAACATGGT | 55213 |
rs148930556 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49556394 | ATGGGGTTTCACCGT[A/G]TTAGCCAGGATGGTC | 55213 |
rs148998522 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49540805 | GTTTTCCATGCCTCA[C/T]GCAAGAAGCGGGGGA | 55213 |
rs149051319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49545675 | GGGGAAATTTTTTTA[A/G]ATTCCAGAGATCCTG | 55213 |
rs149199312 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574201 | TTGGCTCACTGCAAC[C/T]TCCACCTCCCCAGTT | 55213 |
rs149302573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49561703 | GGTAGACAAATTGAT[C/T]AGAAAGTTTAATGGG | 55213 |
rs149317656 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49543123 | CAAAAATTAGCTGGG[C/T]GTGGTTAGTGCACGA | 55213 |
rs149515280 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49575203 | TCAAAACCACAATGA[A/G]ATACTATCTCACACC | 55213 |
rs149547943 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539019 | GGATTACAGGTACGC[A/G]CCACCACACCCAGCT | 55213 |
rs149566845 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581770 | GCATCACAGGCAAGA[C/G]GCATGCTAGTGTCGA | 55213 |
rs149743437 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49556300 | CTCCCGGGTTCATGT[C/T]ATTCTCCTACCTCCC | 55213 |
rs149758789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49537962 | TGTCAAAACGGGGCA[C/T]GGAGGAACCTCAGGT | 55213 |
rs149812729 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539636 | ACCCAATTTAAAATT[A/G]TATCACCGGGTGGAA | 55213 |
rs149827516 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49578467 | GATACCAACAATGCC[A/G]GGGACATCATAAAGA | 55213 |
rs149875162 | snp | A/G | 0.00019887 | 0.00996972 | synonymous-codon, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49541809 | ATACGACTGGAACAT[A/G]GATCGAAAATGCTCA | 55213 |
rs149880080 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583034 | ATAAAAAAATTAGTC[A/G]AATGTGGTGGTGCGC | 55213 |
rs149890299 | in-del | -/CGGCCC | | | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49585668 | CACCGCCCCGGCCCC[-/CGGCCC]GGCCCCGGCCGAAAC | 55213 |
rs150000205 | in-del | -/GCCCCG | 0.000798403 | 0.0199641 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49585657 | CGAGCATCCCGCACC[-/GCCCCG]GCCCCGGCCCCGGCC | 55213 |
rs150021611 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49570203 | ACCACACAACTTCCT[A/G]ACAGCAGCACAATTA | 55213 |
rs150128027 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574664 | ATACAGCTGCTATAG[A/G]AAACCAGATGGTGAT | 55213 |
rs150140298 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581266 | AGGGATTGAAGCCCA[C/T]ACTAGGGAAATGGAG | 55213 |
rs150189495 | snp | C/T | 0.000132048 | 0.00812444 | missense, downstream-variant-500B, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549512 | AGCAGGCAAACACGT[C/T]GTCGGTGCAGGAGAA | 55213 |
rs150192333 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49587095 | CAGAAATAGACTGCG[C/T]ATTTCCTGTAAAAGG | 55213 |
rs150306444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560272 | ACGGGATAGACAGAT[A/G]CAAAATCTTTAAAGA | 55213 |
rs150332958 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49572084 | GTAATTCCAGCACTT[C/T]GGGAGGTAGAGGCAG | 55213 |
rs150384981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49574741 | CTCCATTTCTAGCAT[A/G]TACCCCAAAGAACTG | 55213 |
rs150441748 | snp | A/C/G | 0.000939005 | 0.0216479 | stop-gained, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49566652 | ATGTGGTCCACTCCC[A/C/G]TAACTGAGGCTTTTA | 55213 |
rs150571538 | snp | C/T | 0.00517822 | 0.0506191 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49531979 | TGTTTATTAACATGT[C/T]GTTCTAAATATTACA | 55213 |
rs150624787 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49537558 | AGCAAGATCGTAAGA[A/T]ATAAGTTGCTTAGCA | 55213 |
rs150698684 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49577512 | ACCAGAATGTATTTG[C/T]TTGGGCTAGTTTAAA | 55213 |
rs150747637 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49555405 | CTTTCAATGGAGCTA[C/T]CAAAACAAAGCACTC | 55213 |
rs150781694 | snp | G/T | 0.0379877 | 0.132479 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565324 | ACTCAGTGCTCAATG[G/T]TGCCCAGGCTGGAGT | 55213 |
rs150905324 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49558452 | TTCCCAGCACTTTGG[A/G]AGGCCGAGGCGGGAG | 55213 |
rs150925046 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49550233 | ATCCTCTGCCTTCGC[C/T]TCCCAAAGTGCTGGG | 55213 |
rs151026133 | in-del | -/AATAAATAAAT | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566277 | AAATAAAATAAAATA[-/AATAAATAAAT]AAATAAATAAATAAA | 55213 |
rs151103600 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49567503 | CCACCTTCAAACCCC[A/G]GACTTTCCTACAAGA | 55213 |
rs151191206 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49545985 | CCTCCCTCCACCCCA[G/T]GCAATGCAGAGCTCT | 55213 |
rs151311812 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534949 | TGAGACAGGAGAATC[A/G]TTTGAGCCTGGGAGG | 55213 |
rs180870149 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49543499 | ACTCCCTTAGGTAAG[A/G/T]AATGACATAGGGCTT | 55213 |
rs180895501 | snp | A/T | 0.00398564 | 0.0444627 | utr-variant-5-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49585489 | GCGGGACCGCAGGGA[A/T]CTCCGAAGCTCCAAT | 55213 |
rs180906381 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49575515 | CAACCTAGGTGCCCG[C/T]TGACAGTAGATTGGA | 55213 |
rs180907270 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554570 | TGTTAGGAACCGGGC[A/C]GCACAGCAGGAGGTG | 55213 |
rs181084748 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568999 | ACTATGTGCCAAGCA[A/C]TATTTTTAGAAAATT | 55213 |
rs181130000 | snp | C/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548073 | TGTGAGCCACCACAC[C/G]CAGCCGGTTCTTCAC | 55213 |
rs181138547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559784 | GCATGCTGGTGACAG[C/T]TGTATGACAAGGTGA | 55213 |
rs181190971 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581674 | AGGGACAGGGAGTAC[A/C/G]CCCTAGAAGGGACTG | 55213 |
rs181280063 | snp | C/T | | | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586309 | GCTGCTCCAGCCTAT[C/T]ACCTATAAAGACTAC | 55213 |
rs181298768 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565068 | CTCTGATGCCGAGCC[A/G]AAGCTGGACTGTACT | 55213 |
rs181345431 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49543970 | AGGATTACAGGCATG[A/G]GCCACCATGCTGAGC | 55213 |
rs181427887 | snp | C/T | 0.00271571 | 0.0367489 | missense, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49534228 | ACTTCTGTCAAATGA[C/T]TGATGCAAAACTTAA | 55213 |
rs181453684 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573275 | TCTCCATGGAGAGAT[C/T]ACAGGTGGCATCATT | 55213 |
rs181577579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569952 | ACAAGATGCCCCTCA[A/G]ACGACCTCTTGTGCC | 55213 |
rs181599729 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552994 | CGAGACCATCCTGGC[C/T]AACACAGTGAAACCC | 55213 |
rs181613767 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49537559 | GCAAGATCGTAAGAT[A/G]TAAGTTGCTTAGCAC | 55213 |
rs181724946 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49580194 | AATATCGATGATTAG[A/C]AATAATGTTTTTTCT | 55213 |
rs181764486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548343 | GCAGTGAGCCGAGAT[C/T]GCGCCATTGCACCCC | 55213 |
rs181881189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542955 | TTTAAAGTGAGATAC[A/G]GCACAAAGAGAAAAA | 55213 |
rs181972002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553579 | TAAAGGTTCCAAATA[A/G]CCATAGGAAAAAGTA | 55213 |
rs182015679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581288 | GAAATGGAGAAAATT[A/G]AACAAGAAGGAAAAT | 55213 |
rs182080812 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559080 | CTTAACTCTTGTTTT[C/T]ATCAATTAGCCAATG | 55213 |
rs182085440 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538286 | GCATGAGCCACTGTG[C/T]CCAGCTATGGATTTT | 55213 |
rs182246499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49575075 | GGGGGGAGGTAGGAA[C/T]GGGGAGTTACTGTTT | 55213 |
rs182530709 | snp | C/T | | | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49587588 | CAGGGAGAAACTTCA[C/T]GAGAAGGTCAGTTGG | 55213 |
rs182563149 | snp | C/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49570815 | ATCTTCGTAATACTC[C/T]TGTGAGGAGGAGACT | 55213 |
rs182575769 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49550139 | CTGCACCACCATACC[C/T]GGCTAAGTTTTGTAT | 55213 |
rs182790677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563532 | GCCAGGCATGGTAGC[A/G]TATGCCTCTAATTGT | 55213 |
rs182795682 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566271 | ATAAAAAAATAAAAT[A/T]AAATAAATAAATAAA | 55213 |
rs182797692 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566826 | GCTGTATTAAAAGCT[A/C]CCTTCTCTCCTCTGA | 55213 |
rs182799391 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49545839 | GCTGTTACCAGAGCA[A/C]CTCCTAGAGGAGGGA | 55213 |
rs182863578 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560539 | AAGAGATAGACTGTT[A/T]ACAAAGGAAACAAAA | 55213 |
rs182912764 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539270 | CTCCATGCCCACACT[A/G]TGACAGACTCTGGGG | 55213 |
rs183052856 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583329 | AAGTCTTTAGAGGTA[C/T]CCATCTGGTCTCCTC | 55213 |
rs183119354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535750 | AAACCACAGGCCAGG[C/T]GTGGTGGCTCACGCC | 55213 |
rs183135462 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557236 | CAAGACTGGACAGAC[A/G]GATCAACTTAAAAGA | 55213 |
rs183143338 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535881 | TACAAAAATTAGCCA[A/G]GTGTGGTGGCAAGCA | 55213 |
rs183143591 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49587077 | GATACACCTCACACT[A/G]CCCAGAAATAGACTG | 55213 |
rs183147153 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565653 | TGGGAGGTGAGGAGC[A/G]TCTCTGCCCGGCCGC | 55213 |
rs183147734 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49576728 | CTCACTAAGATAGTA[A/G]TTTTTTTGCAAGCCT | 55213 |
rs183370706 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49540123 | AACCAACCATACCCG[A/C]CTTCAGCTCACTGAT | 55213 |
rs183371194 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49556283 | CTCACTGCCAGCCCC[A/G]CCTCCCGGGTTCATG | 55213 |
rs183385076 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49550807 | GCTACTACTCAAAAC[A/G]CTTTTGCATAGGCCA | 55213 |
rs183399806 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49582291 | CAGGAGTTCGAGACC[A/G]GCCTGGCCAACATGG | 55213 |
rs183400496 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49582557 | TTCCTTTTCTTCCTT[A/C]CACAAGAGGAGGAGG | 55213 |
rs183406727 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49561943 | CTAAAAAAAAAAAAA[A/T]AATACAAAAATCAGC | 55213 |
rs183586631 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49536618 | AAACAGTTCCAAGGA[A/G]GACCAGAAGGATCAT | 55213 |
rs183608720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49578801 | TTCCTAGAAGAACAA[A/G]GTGTTCTTCATAGCC | 55213 |
rs183621527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557737 | CCAGCCTGGGCAACA[C/T]AGCCAGATTCTTGTC | 55213 |
rs183632921 | snp | C/T | 0.00318978 | 0.0398085 | downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49531651 | TCTGTGGCCCGAGGG[C/T]TGGGGACCCCTGACC | 55213 |
rs183676050 | snp | A/C | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49571781 | TACTCAAAATTACCA[A/C]CATCCTCATTATAAT | 55213 |
rs183838649 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573068 | CCCCAAGGAAGCATC[A/C]CAACAGAAGCTGCCA | 55213 |
rs183846064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552688 | AGGTATAATCAAGGC[A/G]CTGCAGAACAGCAAG | 55213 |
rs183868443 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49578174 | CCCTGATAGAAAATG[A/G]CATAGTATTTGCACA | 55213 |
rs183907481 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49544260 | AGATCACCTGAGATC[A/G]GGAGTTCGAGACCAA | 55213 |
rs184007711 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49570569 | TTTGAGCCTGGGTTT[C/T]CCCCAAACCTAGAAA | 55213 |
rs184326951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49547213 | ATACCTAAAGAACAT[A/G]GCAAAAATAAAGTGA | 55213 |
rs184388198 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568746 | CCATCCTGACCAACA[C/T]GGTGAAACCTTATCT | 55213 |
rs184515007 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583586 | GAGTCTCACTGTGTC[A/G]CCCAGGCTGGAGTGC | 55213 |
rs184521233 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563646 | CCTAGGCGATAGAGC[A/G]AGACTGTCTCAAAAG | 55213 |
rs184525744 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542825 | AAAACCTGAGCAGCT[C/G]CTACACTGTATTTAC | 55213 |
rs184705913 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49541319 | GAAAATTAAAATAAG[A/C/T]CCATAGCTTAATACC | 55213 |
rs184746593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49580270 | AGAACAAAAAAACCA[A/G]TGATGGGTCAAAGTT | 55213 |
rs184750723 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49558842 | TAGGAGGTGCCCCTT[A/G]TAATTTTTGCTTTGC | 55213 |
rs184762106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49537564 | ATCGTAAGATATAAG[C/T]TGCTTAGCACACAGG | 55213 |
rs184819485 | snp | A/T | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533573 | TCTTGAAGTTAAAAA[A/T]GTCATCAACGCAAGC | 55213 |
rs184835746 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49579739 | TTCAAGCTGAAGCCA[C/T]CTGTACAGGTGAGTG | 55213 |
rs184902761 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49537132 | AACCAGGGTGAGCAG[G/T]TGCCTCGGCATCACA | 55213 |
rs184946862 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49558346 | TGAACTGGAACAAAC[A/G]GGTTGGAAAATGAAT | 55213 |
rs184963410 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564781 | CAGTAGTCCCAGCTA[C/T]TCGGGAGGCTGAGGC | 55213 |
rs185007439 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583743 | AGTAGAGACGGGGTT[C/T]CACCATGTTGGCCAA | 55213 |
rs185086998 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553174 | CAACAACAACAACAA[A/C]AAGACTAGAAGGAAA | 55213 |
rs185191638 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49573374 | TGTTTTCGTCAGCAG[C/G]GTTGTGGCCAGAAAA | 55213 |
rs185224376 | snp | C/T | 0.0744748 | 0.178019 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559483 | AACACGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 55213 |
rs185257668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49549893 | ATCACACAGACCGCC[A/G]AGGAAAACTTGGAAA | 55213 |
rs185261453 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581420 | ACTGTGCTGCCACTC[A/C/T]CTACAGCAGAAAGCA | 55213 |
rs185372950 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49567065 | CTCTTTATTTATACC[C/T]CGCCTTTTCTCCATC | 55213 |
rs185425243 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568914 | AGCCTGGTGACAGAG[C/T]GAGACTCTGTCTCGA | 55213 |
rs185464684 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49576515 | GAATATAAGTTCAGA[G/T]TAGGGAAATTCTCAA | 55213 |
rs185472733 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49555299 | TACAACTTAGACATA[C/T]AGAATCTTTACTTTC | 55213 |
rs185476846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535360 | TATATTTATTAAATC[A/G]ATTAGGCACCTGGAA | 55213 |
rs185500225 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546918 | GGACCCCTGATCTAG[A/G]AGGATATAGTCAATG | 55213 |
rs185523749 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548076 | GAGCCACCACACCCA[A/G]CCGGTTCTTCACTTT | 55213 |
rs185559207 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569345 | ATGGGAGCCCAAGCC[A/G]GAAGGACTGCTTGAG | 55213 |
rs185618352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49543190 | GATCGCTTGAACACA[A/G]GAGGTGGAGGTTGCA | 55213 |
rs185624714 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49572211 | ATGCACCTGGTGTCC[C/T]AGCTACTTGGGAGGC | 55213 |
rs185773759 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49544001 | CTAGAACATTCTTCA[A/G]TTGGTAATTGCATGT | 55213 |
rs185803602 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586405 | AAACTTGTTGGCATA[A/G]CATTCCAGCCACTTG | 55213 |
rs185817502 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552022 | GTCTTGCTTCTCCTC[A/G]TGGGAAATTAGGGAA | 55213 |
rs185997461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538813 | AGAGGTGAGTCTTTC[C/T]TTTTGTCTTCTTTCT | 55213 |
rs186018677 | snp | A/G/T | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49570622 | ATAATGAAGAAGCTG[A/G/T]GGGATTTCTTGAACA | 55213 |
rs186054585 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49582314 | CAACATGGTGAAACC[C/T]CATCTCTATTAAAAA | 55213 |
rs186125118 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564956 | AGTTGCATTGCAGAA[C/T]AAAGACCAGTGAGCT | 55213 |
rs186248455 | snp | G/T | 0.00318978 | 0.0398085 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49585956 | CCTGCCCACTCTAGA[G/T]CGCGTCTGGCCCCGG | 55213 |
rs186335625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49543600 | GCCACTTTAATGGTC[C/T]TAGCTTATGTGCCTT | 55213 |
rs186360992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581784 | AGGCATGCTAGTGTC[A/G]AATGCTGCTGAGACA | 55213 |
rs186460932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49538946 | GCTGGAGTGCAGTGG[C/T]ACAACTTCTCCCTCC | 55213 |
rs186509789 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49553936 | ATACACAGAGTAACA[C/T]AGAAAATCACCACAA | 55213 |
rs186515644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534800 | GCACTTTGGGAGGCC[A/G]AGGCGGGCGGATCAC | 55213 |
rs186520371 | snp | A/G | 0.00124356 | 0.0249045 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552305 | GAGAGGACAGAAGGG[A/G]GAGAGTGAGATTTTT | 55213 |
rs186536860 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49582898 | CAGTGGAGTGGAGGC[C/T]GGGTGTGGTTGCTCA | 55213 |
rs186563562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49572509 | TAAATTTCATTTAAA[C/T]AATCATTCCAGGCTG | 55213 |
rs186646155 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49559822 | TAACACCACTGAACT[A/G]TACACTTAAAACTGG | 55213 |
rs186749967 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49578956 | GTAAACTTTGGTATA[A/C]AACATTACAACTTAA | 55213 |
rs186935930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49570209 | CAACTTCCTGACAGC[A/G]GCACAATTATTCTAA | 55213 |
rs186943450 | snp | A/C | 5.02113e-05 | 0.0050103 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534291 | AAAAATAAAAACAAA[A/C]ATGGCTTTTTTAGGC | 55213 |
rs187146188 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548514 | ATACAAGAACAGTCA[C/T]GACAGCACTACCCAC | 55213 |
rs187183423 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49587184 | CTGGGTTTAGAACAG[C/T]GCCTGGCATGTGATA | 55213 |
rs187184375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49550192 | CTATATTGCCAGGGC[C/T]GGTCACCAACTCCTG | 55213 |
rs187190589 | snp | G/T | 0.00119737 | 0.0244387 | downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49531527 | AATCTAATGTTCTAA[G/T]GTTGCCACTGATCTG | 55213 |
rs187198995 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49544337 | AGCCAGGCATGGTGG[C/T]GCCTGCCTGTAATCC | 55213 |
rs187296290 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49575116 | GAGTTTCACTTTGGG[G/T]TGATGAAAAAGTTCT | 55213 |
rs187394404 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566883 | CAGGAGGTGAAAAGA[A/G]ACTGATATGGTTGTT | 55213 |
rs187403564 | snp | A/C | | | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49546695 | AACCTGTATCCCTCG[A/C]ATGTGCAGTTCACAA | 55213 |
rs187412573 | snp | C/G | 0.0352966 | 0.128072 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49565711 | ACCCGGCAGCCACCC[C/G]GTCTGAGAAGTGAGG | 55213 |
rs187485757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49562982 | CAGAAATGACCAATA[C/T]AATAAATTAAAAATT | 55213 |
rs187498013 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49539644 | TAAAATTATATCACC[A/G]GGTGGAAATAAAATC | 55213 |
rs187534972 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49560983 | ACCAACCCGGAAGCT[A/C]CTCTGTCTGAATTTT | 55213 |
rs187762246 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535962 | CAGGAGGCGGAGGTT[G/T]CAGTGAGCCGAGATC | 55213 |
rs187764161 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49537006 | ACAGAGCATTGATGG[G/T]CTTAATATCCTCATT | 55213 |
rs187767362 | snp | C/T | 3.33067e-05 | 0.00408072 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49566607 | AAAAGTTAGATGGGT[C/T]CCCTCCTTACCTTCG | 55213 |
rs187795527 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | RCBTB1 | GRCh38.p7 | 13:49540763 | ATGGGTTCACTGATT[A/C]CCTAAACAGAAGTGG | 55213 |
rs187798224 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49578191 | ATAGTATTTGCACAT[A/G]ACCTACACACATCCT | 55213 |
rs187802788 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557389 | GGAGATGGTACAAAA[G/T]ATTAGAAGACAGAAT | 55213 |
rs187989705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49557830 | GATTATACAATACAC[A/G]TTATGCTAGAGAGAG | 55213 |
rs188006467 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583437 | TGATCTAACACACAG[C/T]TGACTTATATAATTA | 55213 |
rs188015255 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49533675 | GCACTTAACAATCCC[C/T]AGGTCAGCATCTTTA | 55213 |
rs188056271 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49545621 | GCTTTCTTGTGTTTT[A/G]TATGTATGAAAGAAG | 55213 |
rs188255341 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49547261 | GTTTCACTTTAAGGC[A/T]AGCTTAACTCTTCCT | 55213 |
rs188296961 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49563612 | TACAGTGAGCTGAGA[C/T]CGTGCCACTGCACTC | 55213 |
rs188300831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49568943 | GAAAATAAAAAATAA[C/T]GATCAGAATAATTGC | 55213 |
rs188303586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49556619 | CCCACCCTGCTTCAC[A/G]TGGCTGCAGGAGGTG | 55213 |
rs188495796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49572016 | ACTTAAGAACTGTGC[A/G]GTTAACAATGACTCA | 55213 |
rs188504680 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49543933 | ATCAAGTGATATTCC[C/T]GCCTTGGCCTCCCAA | 55213 |
rs188520913 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49552980 | CCAGGTCAGGAGATC[A/G]AGACCATCCTGGCCA | 55213 |
rs188536902 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49577728 | CTTTATTATGGAAGC[C/T]GATAGCCAGAGGAAA | 55213 |
rs188565734 | snp | C/T | 0.0134861 | 0.0810011 | utr-variant-3-prime, nc-transcript-variant | RCBTB1 | GRCh38.p7 | 13:49532266 | CAAATGACTTAGTAA[C/T]CTAATATGAGAAGTG | 55213 |
rs188600960 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49535751 | AACCACAGGCCAGGC[A/G]TGGTGGCTCACGCCT | 55213 |
rs188759649 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49569830 | GAGGATTGCTTGAAC[C/G]CAGGAAGTCAAGGCT | 55213 |
rs188765488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49548077 | AGCCACCACACCCAG[C/T]CGGTTCTTCACTTTT | 55213 |
rs188841642 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49551584 | ATCATCAGGGGTGGA[C/T]TGACATTTGCTGGAA | 55213 |
rs189052996 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564884 | CGACAGAGAGAGACT[C/T]CGTCTCAAAAAAAAA | 55213 |
rs189179597 | snp | A/C/T | 0.00875054 | 0.0656008 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49564543 | TGGGCCGAGATCATG[A/C/T]CACTGCACTCCAGCC | 55213 |
rs189187520 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49542855 | CATGTACAAAGCCAC[C/G]TGCACAAGAAACTGA | 55213 |
rs189213636 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49583592 | CACTGTGTCGCCCAG[A/G]CTGGAGTGCAGTGGC | 55213 |
rs189281859 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49584705 | AGATCATGAATCTGG[C/T]TTTCTAAAAGCATTA | 55213 |
rs189343513 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49543391 | TCATGGTCAGAAAAC[A/T]GTACATGAAAGGAAT | 55213 |
rs189423204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49581198 | CACAGAGACATGAGA[C/T]GACAAAGGAGTGCTT | 55213 |
rs189425061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49558968 | TTAATCTTTGTTAAA[C/T]ATATGTATTAGTTTG | 55213 |
rs189433010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49537855 | ATAGCAAGGGATCCA[C/T]AATCATCAACTTACT | 55213 |
rs189565215 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | RCBTB1 | GRCh38.p7 | 13:49586145 | GTATGAAGGAAGGAC[A/G]AGATGAGGCACAGGT | 55213 |
rs189651375 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49575314 | TAGTGGGAATGTAAA[C/T]TAGTTCAGCCACTGT | 55213 |
rs189659432 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCBTB1 | GRCh38.p7 | 13:49554136 | CAGGCTGAAGAATAG[C/T]AGAGAAAAGCTGCAG | 55213 |
rs189670200 | snp | A/G | | | intron-variant | RCBTB1 | GRCh38.p7 | 13:49534832 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 55213 |