SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs7593 | snp | A/G | 0.45856 | 0.13785 | synonymous-codon | RBBP6 | GRCh38.p7 | 16:24572085 | AATAGTGGAGAAAGC[A/G]AAAGAGAGCCTGGAC | 5930 |
rs1056259 | snp | A/G | 0 | 0 | intron-variant | RBBP6 | GRCh38.p7 | 16:24554748 | GTGGGGAGGAGTTGG[A/G]GCGGTTTGGGGGATT | 5930 |
rs1063640 | snp | A/G | | | synonymous-codon | RBBP6 | GRCh38.p7 | 16:24572262 | gaagaagaagaaaaa[A/G]aaggaaaagaaaaaA | 5930 |
rs1991474 | snp | C/T | 0.403509 | 0.197319 | intron-variant | RBBP6 | GRCh38.p7 | 16:24551598 | TTTTAAGCTTTCTGC[C/T]AACTTATTAGTATTA | 5930 |
rs1991475 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | RBBP6 | GRCh38.p7 | 16:24551304 | TACTAATGGTAAAAA[A/G]AAGTCTGCCACTTAA | 5930 |
rs2033214 | snp | A/C | 0.319136 | 0.24025 | intron-variant | RBBP6 | GRCh38.p7 | 16:24566199 | CAACAGTAGGGGTTT[A/C]GATTTTAAGCATCTT | 5930 |
rs3214553 | in-del | -/A | 0.414245 | 0.188477 | intron-variant | RBBP6 | GRCh38.p7 | 16:24546298 | AAAATTAAAAAAACT[-/A]AAAAAAAGTCTATTT | 5930 |
rs3743968 | snp | A/T | 3.34644e-05 | 0.00409036 | missense | RBBP6 | GRCh38.p7 | 16:24570313 | CTGTTGAGTTTGATT[A/T]TTTTGGCTGGCGCAC | 5930 |
rs3760101 | snp | G/T | | | intron-variant | RBBP6 | GRCh38.p7 | 16:24541205 | GAAAATTGTTTTTTT[G/T]GTTTTTTTTTTGTTT | 5930 |
rs3760102 | snp | G/T | 0.341909 | 0.232492 | intron-variant | RBBP6 | GRCh38.p7 | 16:24541204 | AAAATTGTTTTTTTG[G/T]TTTTTTTTTTGTTTT | 5930 |
rs3760103 | snp | G/T | 0.46754 | 0.123192 | intron-variant | RBBP6 | GRCh38.p7 | 16:24541193 | TTTGGTTTTTTTTTT[G/T]TTTTTTTTTTTGCTG | 5930 |
rs3764975 | snp | A/C | 0.00429733 | 0.0461541 | intron-variant | RBBP6 | GRCh38.p7 | 16:24563341 | GCCAGAAAAACAAAA[A/C]CCTGCTGTAAAAAAA | 5930 |
rs3809681 | snp | G/T | 0.41408 | 0.188621 | intron-variant | RBBP6 | GRCh38.p7 | 16:24554750 | CCAATCCCCCAAACC[G/T]CCCCAACTCCTCCCC | 5930 |
rs3815906 | snp | A/G | 0.367091 | 0.220884 | intron-variant | RBBP6 | GRCh38.p7 | 16:24559436 | GCTACATGTTCTACT[A/G]TAACATAATGGGAAC | 5930 |
rs3840856 | in-del | -/A | | | intron-variant | RBBP6 | GRCh38.p7 | 16:24554766 | AAACAAAAAAAAAAA[-/A]CCAATCCCCCAAACC | 5930 |
rs7186649 | snp | G/T | 0.0376037 | 0.131863 | intron-variant | RBBP6 | GRCh38.p7 | 16:24542589 | tcagcctcccaagta[G/T]ctgggactacaggca | 5930 |
rs7186715 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | RBBP6 | GRCh38.p7 | 16:24542788 | ATAGTTAAAAGAATC[C/T]TGTCCGGAAATTTAA | 5930 |
rs7194163 | snp | G/T | 0.366473 | 0.221211 | intron-variant | RBBP6 | GRCh38.p7 | 16:24567009 | AATTGTACTAATGTT[G/T]CTACACTAGTTGAAT | 5930 |
rs7195386 | snp | C/T | 0.491443 | 0.0648475 | intron-variant | RBBP6 | GRCh38.p7 | 16:24567137 | TCTTGGAATTTATTT[C/T]TCCAGAAGTATAAAC | 5930 |
rs7196506 | snp | A/G | 0.140581 | 0.224783 | intron-variant | RBBP6 | GRCh38.p7 | 16:24570727 | TCATAATCTTAAATT[A/G]TGTGTCTTCCTTAGG | 5930 |
rs7196581 | snp | C/G | 0.138546 | 0.223781 | intron-variant | RBBP6 | GRCh38.p7 | 16:24540858 | CTAGAAGGTGCCTGG[C/G]AGGAAGCTAACCGCC | 5930 |
rs7196736 | snp | C/G | 0.264734 | 0.249579 | synonymous-codon | RBBP6 | GRCh38.p7 | 16:24570978 | TAATAATGACAATAC[C/G]GCGCCAGCTGAAGAT | 5930 |
rs7200471 | snp | A/C | 0.226188 | 0.248863 | intron-variant | RBBP6 | GRCh38.p7 | 16:24568195 | GGGAATAGCCAAAAA[A/C]CAGTTCCCAGGACCC | 5930 |
rs7200560 | snp | A/T | 0.465052 | 0.127485 | intron-variant | RBBP6 | GRCh38.p7 | 16:24559060 | TGAGAGACTTTTGGG[A/T]TATGGAGAAGGGGAG | 5930 |
rs7201851 | snp | C/T | 0.428786 | 0.174744 | intron-variant | RBBP6 | GRCh38.p7 | 16:24568076 | GTCTCAGTGTAAATT[C/T]TATTGTGTAGAACTA | 5930 |
rs7202501 | snp | A/G | 0.41408 | 0.188621 | intron-variant | RBBP6 | GRCh38.p7 | 16:24555999 | TTATTTTTCTTGGTT[A/G]ATACTGCCTTCTGTA | 5930 |
rs7202917 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | RBBP6 | GRCh38.p7 | 16:24556155 | ggagataaaatagta[C/T]gtacttcacatagca | 5930 |
rs7204806 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | RBBP6 | GRCh38.p7 | 16:24551195 | CATAAAAGATTTTAG[A/G]TCCTTGCTTCCCAAA | 5930 |
rs7206159 | snp | C/T | 0.445328 | 0.156035 | intron-variant | RBBP6 | GRCh38.p7 | 16:24551137 | TAAATATCAGAGTGG[C/T]ATTTTATAGGATTCT | 5930 |
rs8044750 | snp | A/G | 0.414245 | 0.188477 | intron-variant | RBBP6 | GRCh38.p7 | 16:24547956 | TGTACAATATATAGG[A/G]TTCTGTTTGTAATAA | 5930 |
rs8045499 | snp | G/T | 0.139225 | 0.224118 | intron-variant | RBBP6 | GRCh38.p7 | 16:24548348 | tgtttttaagagatg[G/T]ggtcactatgttaca | 5930 |
rs8049497 | snp | A/G | 0.414245 | 0.188477 | intron-variant | RBBP6 | GRCh38.p7 | 16:24548553 | AATGTTAACAACAGC[A/G]GTCTTCCTGATGTGT | 5930 |
rs8059872 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | RBBP6 | GRCh38.p7 | 16:24545342 | ctcccaaaatgctgg[G/T]attacaggcgtgaac | 5930 |
rs8061498 | snp | G/T | 0.0360663 | 0.129354 | intron-variant | RBBP6 | GRCh38.p7 | 16:24541972 | TCCATTTACAATGCA[G/T]ACCTAAGTATAATTG | 5930 |
rs8064215 | snp | G/T | 0.0345262 | 0.126772 | upstream-variant-2KB | RBBP6 | GRCh38.p7 | 16:24538802 | AGCTATTAATATTTC[G/T]GTGCATTGAGCCACG | 5930 |
rs8064222 | snp | A/G/T | 0.0345262 | 0.126772 | upstream-variant-2KB | RBBP6 | GRCh38.p7 | 16:24538803 | GCTATTAATATTTCG[A/G/T]TGCATTGAGCCACGT | 5930 |
rs9922288 | snp | A/G | 0.343477 | 0.231866 | utr-variant-5-prime | RBBP6 | GRCh38.p7 | 16:24539609 | CGCGTCCGCCATAGT[A/G]CCTGGCTTGGAGGTG | 5930 |
rs9923179 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | RBBP6 | GRCh38.p7 | 16:24557517 | AACTTTGTTGAGCAT[A/G]AGAATTTCCTACAAA | 5930 |
rs9923363 | snp | A/G | 0.413914 | 0.188765 | intron-variant | RBBP6 | GRCh38.p7 | 16:24557546 | AAAGTATGTTAAAAG[A/G]CTGGCCAGGTAGAGG | 5930 |
rs9924061 | snp | C/T | 0.398714 | 0.200958 | intron-variant | RBBP6 | GRCh38.p7 | 16:24543443 | ACACACCACCATGCC[C/T]GGCTAATTTATTGTA | 5930 |
rs9926381 | snp | C/G | 0.301654 | 0.246421 | intron-variant | RBBP6 | GRCh38.p7 | 16:24558873 | CTATAAATTGATTAA[C/G]CTCTCTTAAAATACT | 5930 |
rs9927702 | snp | A/G | 0.465158 | 0.127307 | intron-variant | RBBP6 | GRCh38.p7 | 16:24547332 | AGTATCTTCCATATA[A/G]TAGCTACTTTAAAAA | 5930 |
rs9929910 | snp | C/T | 0.414245 | 0.188477 | intron-variant | RBBP6 | GRCh38.p7 | 16:24545496 | CTTTCTGTCATTCTT[C/T]TCTTTTATTTTCTTA | 5930 |
rs9931525 | snp | C/T | 0.41408 | 0.188621 | intron-variant | RBBP6 | GRCh38.p7 | 16:24557041 | TCTCGCTCTGTCCCT[C/T]AGGCTGAAGTGCAGT | 5930 |
rs9937097 | snp | A/G | 0.414245 | 0.188477 | intron-variant | RBBP6 | GRCh38.p7 | 16:24544915 | ATCTCCCCCATATTC[A/G]GTCCATCAGCAAGCT | 5930 |
rs9937187 | snp | C/G | 0.367503 | 0.220665 | intron-variant | RBBP6 | GRCh38.p7 | 16:24545013 | TACCTGGATTTTTTA[C/G]CAGCCTGGTTATTAG | 5930 |
rs9937315 | snp | C/G | 0.298144 | 0.245321 | intron-variant | RBBP6 | GRCh38.p7 | 16:24545320 | CTCGTGATCCGCCCC[C/G]CTCAGCCTCCCAAAA | 5930 |
rs9937985 | snp | G/T | 0.413582 | 0.189052 | intron-variant | RBBP6 | GRCh38.p7 | 16:24553800 | TGAAGCTACACTTAA[G/T]TATTTTTTTTCCCTC | 5930 |
rs9939499 | snp | A/C | 0.414245 | 0.188477 | intron-variant | RBBP6 | GRCh38.p7 | 16:24545508 | CTTTTCTTTTATTTT[A/C]TTAGGCTCTTCAAGC | 5930 |
rs9939968 | snp | A/G | 0.413914 | 0.188765 | intron-variant | RBBP6 | GRCh38.p7 | 16:24545850 | TTCATTCCGAATAAC[A/G]GCTTTTTCACCATTC | 5930 |
rs9941222 | snp | C/T | 0.298398 | 0.245271 | intron-variant | RBBP6 | GRCh38.p7 | 16:24557139 | gagtagctgggacta[C/T]aggcgcccgccacca | 5930 |
rs10431902 | snp | C/T | 0.287606 | 0.247155 | intron-variant | RBBP6 | GRCh38.p7 | 16:24542457 | ACAATTGAATGCAGC[C/T]TTTTTTTTTTTTTTC | 5930 |
rs10521126 | snp | A/G | 0.367091 | 0.220884 | intron-variant | RBBP6 | GRCh38.p7 | 16:24553938 | TTCCTTTACACGGAC[A/G]ATTGCATGGTTATTT | 5930 |
rs10677916 | in-del | -/T | | | intron-variant | RBBP6 | GRCh38.p7 | 16:24548331 | GTTTTTTTTTTTTTT[-/T]CTGTTTTTAAGAGAT | 5930 |
rs11074632 | snp | C/T | | | intron-variant | RBBP6 | GRCh38.p7 | 16:24551894 | GTAACTTCTGGTTGG[C/T]ATAAAATCTTTAAAA | 5930 |
rs11074633 | snp | G/T | 0.29789 | 0.24537 | intron-variant | RBBP6 | GRCh38.p7 | 16:24551948 | TTTTAGATAAAAAGA[G/T]ATATGTATTATTTAG | 5930 |
rs11282687 | in-del | -/CCTGGG | | | utr-variant-5-prime | RBBP6 | GRCh38.p7 | 16:24540079 | GGGCCTGGGCCTGGG[-/CCTGGG]GAAGCTGACGCCGGT | 5930 |
rs11311859 | in-del | -/A | 0.0352966 | 0.128072 | upstream-variant-2KB | RBBP6 | GRCh38.p7 | 16:24538474 | TCAGAGAGGATGAGG[-/A]ACATGGATTGTAAAC | 5930 |
rs11375359 | in-del | -/G | 0.226188 | 0.248863 | intron-variant | RBBP6 | GRCh38.p7 | 16:24562995 | GTATCTTCTTAAGGA[-/G]GGTCCTTCATTTTAC | 5930 |
rs11550905 | snp | A/T | 0.194278 | 0.243711 | utr-variant-3-prime | RBBP6 | GRCh38.p7 | 16:24572810 | AGTGACATAACAGGG[A/T]TGTAATGAATTCAGC | 5930 |
rs11642048 | snp | A/C | 0.223225 | 0.248562 | intron-variant | RBBP6 | GRCh38.p7 | 16:24565649 | gtggaacagttttta[A/C]ccccctgcccccgtc | 5930 |
rs11860248 | snp | G/T | 0.369346 | 0.219673 | intron-variant | RBBP6 | GRCh38.p7 | 16:24566445 | AAGAGGTTACAGGAG[G/T]TGGTTTTCCTTCATT | 5930 |
rs12051373 | snp | A/G | 0.193653 | 0.243567 | intron-variant, downstream-variant-500B | RBBP6 | GRCh38.p7 | 16:24549672 | TGGGGCCCCCTATGA[A/G]TATATAAGTGTCTTA | 5930 |
rs12149378 | snp | A/G | 0.112631 | 0.208878 | intron-variant | RBBP6 | GRCh38.p7 | 16:24560179 | cagtggtgtaatctc[A/G]gctcactgcatcctc | 5930 |
rs12149382 | snp | G/T | 0.412416 | 0.190055 | intron-variant | RBBP6 | GRCh38.p7 | 16:24560275 | CCACACCCGGCTAAT[G/T]TTTTGTATTTTTAGT | 5930 |
rs12185161 | snp | C/T | 0.367708 | 0.220556 | intron-variant | RBBP6 | GRCh38.p7 | 16:24547019 | GCTTTCTTGCAATTT[C/T]AGTAGTGATAGCAGA | 5930 |
rs13329830 | snp | C/T | 0.392325 | 0.205532 | intron-variant | RBBP6 | GRCh38.p7 | 16:24542471 | CTTTTTTTTTTTTTT[C/T]CCCCTGAAACAGAGT | 5930 |
rs13330463 | snp | C/T | 0.412416 | 0.190055 | intron-variant | RBBP6 | GRCh38.p7 | 16:24560843 | TTTGGGGCAGTTGAG[C/T]GACTTGAGCATCTAC | 5930 |
rs13330500 | snp | C/T | 0.412416 | 0.190055 | intron-variant | RBBP6 | GRCh38.p7 | 16:24560879 | TTATCTTCAGAGGGT[C/T]CTGGAACCCATCCCC | 5930 |
rs13331621 | snp | G/T | 0.367503 | 0.220665 | intron-variant | RBBP6 | GRCh38.p7 | 16:24544307 | AATTTGGGGCTATCA[G/T]GAACTGTCCAAGATA | 5930 |
rs13332826 | snp | A/G | 0.298144 | 0.245321 | intron-variant | RBBP6 | GRCh38.p7 | 16:24546871 | ACTCTAGAGGGTTGT[A/G]AGAATTAAATAGTGT | 5930 |
rs13332926 | snp | G/T | 0.414245 | 0.188477 | intron-variant | RBBP6 | GRCh38.p7 | 16:24546866 | ACTTAACTCTAGAGG[G/T]TTGTAAGAATTAAAT | 5930 |
rs13335066 | snp | A/T | 0.364817 | 0.222075 | intron-variant | RBBP6 | GRCh38.p7 | 16:24560685 | ACAGTAAAAAATAAT[A/T]GTAAAGACTAATACA | 5930 |
rs13335590 | snp | C/T | | | synonymous-codon | RBBP6 | GRCh38.p7 | 16:24569627 | GTTTGTTCTCCCAAG[C/T]AGAGATGATGCCACA | 5930 |
rs16973781 | snp | A/G | 0.140919 | 0.224948 | upstream-variant-2KB | RBBP6 | GRCh38.p7 | 16:24538748 | TGTCATGTTGACCAC[A/G]TAGGGTTTTTGTTGT | 5930 |
rs16973796 | snp | C/G | 0.00369684 | 0.0428341 | missense | RBBP6 | GRCh38.p7 | 16:24540753 | AAGCTGAAAGCTGCC[C/G]ACTGCGACCTGCAGA | 5930 |
rs16973822 | snp | C/T | 0.139564 | 0.224285 | intron-variant | RBBP6 | GRCh38.p7 | 16:24546950 | ACAACTAGTCCGGAG[C/T]TGGTATTCACTAACC | 5930 |
rs16973825 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | RBBP6 | GRCh38.p7 | 16:24554647 | TATAGAGTTAACACT[C/T]AGAAGTTTATAGTTT | 5930 |
rs16973827 | snp | G/T | 0.138886 | 0.22395 | intron-variant | RBBP6 | GRCh38.p7 | 16:24555997 | TCTTATTTTTCTTGG[G/T]TAATACTGCCTTCTG | 5930 |
rs16973830 | snp | A/G | 0.139225 | 0.224118 | intron-variant | RBBP6 | GRCh38.p7 | 16:24557395 | ATAACCTCCCATTTT[A/G]TCTGCTTTTATTAAT | 5930 |
rs16973831 | snp | A/C | 0.0304395 | 0.119554 | synonymous-codon | RBBP6 | GRCh38.p7 | 16:24561625 | AGGTATAAGAACAGC[A/C]CTCCTGGAATCAGAT | 5930 |
rs16973832 | snp | A/G | 0.0128846 | 0.0792231 | intron-variant | RBBP6 | GRCh38.p7 | 16:24564791 | ATTTTTTTTTCTCCC[A/G]CACAGTTCCAACAAA | 5930 |
rs16973840 | snp | C/T | 0.0366586 | 0.130328 | missense | RBBP6 | GRCh38.p7 | 16:24567217 | TACCAGCAACTCCAG[C/T]CTTTGTACCTGTTCC | 5930 |
rs17768065 | snp | C/T | 0.299158 | 0.245119 | utr-variant-5-prime | RBBP6 | GRCh38.p7 | 16:24539725 | TTGCGGGCGTGTTCT[C/T]GCGGTTCCGGGCCTC | 5930 |
rs17830478 | snp | A/G | 0.0139853 | 0.0824443 | intron-variant | RBBP6 | GRCh38.p7 | 16:24559010 | TAATTTTAATTTCCC[A/G]TCTTGTGGCATTTAC | 5930 |
rs28361295 | snp | G/T | | | intron-variant | RBBP6 | GRCh38.p7 | 16:24550378 | GTTTTTTTGTTTTTT[G/T]TTTTTAAGCATAATG | 5930 |
rs28361950 | snp | A/G | 0.38286 | 0.211774 | upstream-variant-2KB | RBBP6 | GRCh38.p7 | 16:24538496 | ATTGTAAACGATAAT[A/G]ACTATCGTTTATGAA | 5930 |
rs28372136 | snp | C/T | | | intron-variant | RBBP6 | GRCh38.p7 | 16:24550170 | TACTATTGCTCTTTG[C/T]ATATGAGGCATTTCA | 5930 |
rs28401342 | snp | C/G | 0.298651 | 0.24522 | intron-variant | RBBP6 | GRCh38.p7 | 16:24553071 | GCAATTATATGGGAG[C/G]TGTTATTTATTAAAG | 5930 |
rs28451746 | snp | G/T | 0.00988468 | 0.0696034 | intron-variant | RBBP6 | GRCh38.p7 | 16:24570522 | AGTGTAGGGGGTGGG[G/T]GTGGAACTTTGTTGG | 5930 |
rs28452855 | snp | C/T | 0.295343 | 0.245854 | intron-variant | RBBP6 | GRCh38.p7 | 16:24561153 | TGTCTTTCTAGACTA[C/T]CTTATATTTCTCTTT | 5930 |
rs28470964 | snp | C/G | | | intron-variant, downstream-variant-500B | RBBP6 | GRCh38.p7 | 16:24549851 | CCTTATCAGAGGTAA[C/G]TCCCCTTAACCAGGA | 5930 |
rs28482789 | snp | A/C | 0.414245 | 0.188477 | intron-variant | RBBP6 | GRCh38.p7 | 16:24543747 | AACTTTTCTGCACAC[A/C]GACCCCTAAAAAACA | 5930 |
rs28538344 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RBBP6 | GRCh38.p7 | 16:24550372 | TTTTTTGTTTTTTTG[G/T]TTTTTTTTTTTAAGC | 5930 |
rs28540819 | snp | C/T | 0.205723 | 0.246048 | downstream-variant-500B | RBBP6 | GRCh38.p7 | 16:24573322 | AGCGGTCATTACTTA[C/T]GATGAGTTTCCTTTA | 5930 |
rs28553362 | snp | A/C | 0.0752113 | 0.178743 | intron-variant | RBBP6 | GRCh38.p7 | 16:24562701 | AAAAAAAAAAAAAAA[A/C]GGTGTAAGAGGCCCA | 5930 |
rs28600990 | snp | C/T | 0.414245 | 0.188477 | intron-variant | RBBP6 | GRCh38.p7 | 16:24543840 | AAATGACCCTTGTCA[C/T]CTTTCTTACTCTCCA | 5930 |
rs28640970 | snp | A/G | 0.414245 | 0.188477 | intron-variant | RBBP6 | GRCh38.p7 | 16:24544023 | TAGAAAGATACTTTG[A/G]GGGGTAAGAAATCAT | 5930 |
rs28683552 | snp | A/G | 0.198634 | 0.244666 | downstream-variant-500B | RBBP6 | GRCh38.p7 | 16:24572981 | CTTAGTTTTTAATAC[A/G]AGCTGAACTGAATAT | 5930 |
rs34473709 | in-del | -/TT | 0.387017 | 0.209109 | intron-variant | RBBP6 | GRCh38.p7 | 16:24561564 | TCATTTCGTAAACAC[-/TT]TGAGTTCCTACTATG | 5930 |