SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs733329 | snp | A/G | 0.44333 | 0.158505 | intron-variant | RC3H2 | GRCh38.p7 | 9:122861885 | ATATCTTTATACTCT[A/G]AACCCTTACGTTTGT | 54542 |
rs1053762 | snp | A/T | 0 | 0 | stop-gained | RC3H2 | GRCh38.p7 | 9:122855271 | TGGGGTGCGATTTCC[A/T]GATCTTCCCGTACAG | 54542 |
rs1147318 | snp | A/G | 0.470908 | 0.117046 | upstream-variant-2KB | RC3H2 | GRCh38.p7 | 9:122906529 | TTTTTTTGTTGAGAC[A/G]GAGTCTGGCACTGCC | 54542 |
rs1147319 | snp | G/T | 0.487933 | 0.0767327 | upstream-variant-2KB | RC3H2 | GRCh38.p7 | 9:122907223 | ccgtcatcatgcccg[G/T]ctaaatttctttttt | 54542 |
rs1147320 | snp | C/T | | | upstream-variant-2KB | RC3H2 | GRCh38.p7 | 9:122907254 | gtatttttgtagaga[C/T]gggttttcaccatgt | 54542 |
rs1375861 | snp | A/C/G | 0.00279162 | 0.0372561 | intron-variant | RC3H2 | GRCh38.p7 | 9:122854855 | CAGCCTCGCAAAGTG[A/C/G]TGGGATTACATATGT | 54542 |
rs1375862 | snp | C/T | 0.429688 | 0.173817 | intron-variant | RC3H2 | GRCh38.p7 | 9:122854758 | CCTCCATTTAACAAC[C/T]ATGGGAAACTCAGAA | 54542 |
rs1545426 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | RC3H2 | GRCh38.p7 | 9:122900007 | TGGGGGAGTTTCAAC[C/T]ATACAGAAAAATGCT | 54542 |
rs1823448 | snp | C/G | 0.439085 | 0.163545 | intron-variant | RC3H2 | GRCh38.p7 | 9:122855112 | TTTTTTTTTTTAATT[C/G]AGACAGAGTCTCACT | 54542 |
rs1823449 | snp | A/C | 0.438105 | 0.164671 | intron-variant | RC3H2 | GRCh38.p7 | 9:122855018 | AAGCGATTCTCCTGC[A/C]TCAGCCTCCCAAGTA | 54542 |
rs1823450 | snp | C/T | 0.438246 | 0.16451 | intron-variant | RC3H2 | GRCh38.p7 | 9:122854973 | CATGCACCACCATGC[C/T]TGGCTAATTTTTGTA | 54542 |
rs1947247 | snp | C/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122854890 | tctggaactcctggc[C/T]tcatgtgatccaccc | 54542 |
rs1971886 | snp | A/T | 0.0535932 | 0.154675 | intron-variant | RC3H2 | GRCh38.p7 | 9:122900240 | TTTAAGATATAAAGG[A/T]AAAACACTGCCAAAA | 54542 |
rs2215843 | snp | A/C | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122854822 | GCCACTGTGCCTGTC[A/C]TAAGCACTGTGCTTT | 54542 |
rs2251495 | snp | C/T | 0.46754 | 0.123192 | intron-variant, upstream-variant-2KB | RC3H2, SNORD90 | GRCh38.p7 | 9:122880408 | GATGCAACAGGGAAA[C/T]AAATACATGATACTA | 54542 |
rs2252419 | snp | A/G | 0.137867 | 0.223442 | intron-variant | RC3H2 | GRCh38.p7 | 9:122873326 | GTGAAGCTGGTTGGA[A/G]ATAAGAAGTAAGAAC | 54542 |
rs2298015 | snp | C/T | 0 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122850992 | TTTGGCTTTATGCTG[C/T]GAGGGGAAGACCTTA | 54542 |
rs2430382 | snp | A/C | 0 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122899091 | AAAAAAAAAAAAAAA[A/C]CACAATAAAGGCTAA | 54542 |
rs2442765 | snp | C/T | 0 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122866688 | tgagtgaaccagaca[C/T]cgtctgcaatcccgg | 54542 |
rs2487385 | snp | A/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122867253 | gtcagccccccgccc[A/G]gccagccgccccgtc | 54542 |
rs2487386 | snp | A/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122867366 | ctactgggaagtgag[A/G]agcccctctgcccag | 54542 |
rs2539927 | snp | C/G | 0.0535932 | 0.154675 | intron-variant | RC3H2 | GRCh38.p7 | 9:122900322 | AAGGGAAGTTTAGTT[C/G]ATAATTTACTGTCAG | 54542 |
rs2539928 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | RC3H2 | GRCh38.p7 | 9:122895995 | TTGAACATTAGGGGG[A/G]AAAAAAAAAAGAACA | 54542 |
rs2539929 | snp | A/G | 0.0707826 | 0.174302 | | | GRCh38.p7 | 9:122884002 | cggccTAAtttttat[A/G]tatttgtttgagatg | 54542 |
rs2539930 | snp | C/T | 0 | 0 | | | GRCh38.p7 | 9:122861505 | tttttcttttctttt[C/T]ttttttttttttttg | 54542 |
rs2596690 | snp | A/T | | | | | GRCh38.p7 | 9:122868642 | acaagtgaacagagg[A/T]ctctggttttcctag | 54542 |
rs2596691 | snp | A/G | 0.0532157 | 0.154195 | | | GRCh38.p7 | 9:122864765 | GGCATGGTGGCGGGC[A/G]TATGTAGTCCCAGCT | 54542 |
rs2596692 | snp | A/G | 0.485866 | 0.0828688 | | | GRCh38.p7 | 9:122862702 | TCGCCATGTTGGCCA[A/G]ACTGGTCTAGAACTC | 54542 |
rs2596693 | snp | C/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 9:122905260 | TACAGGGACAGCCCC[C/G]TTGGCGCGGCGAAGG | 54542 |
rs2596697 | snp | A/T | 0.0509478 | 0.151255 | | | GRCh38.p7 | 9:122876704 | ACTAAGACTTTCATT[A/T]TTGAGACCTCACCAA | 54542 |
rs2596698 | snp | A/G | 0.00900288 | 0.066486 | | | GRCh38.p7 | 9:122875369 | TGTCTATCTTACATA[A/G]GTGTAACCCCCGTGG | 54542 |
rs2596699 | snp | A/T | 0.0113051 | 0.0743286 | | | GRCh38.p7 | 9:122875192 | TTTCCCCACTTGAAG[A/T]GCCTAGAGAAGAGGA | 54542 |
rs2596701 | snp | G/T | 0.467439 | 0.123371 | | | GRCh38.p7 | 9:122888734 | CCTGAATGCCTATGC[G/T]TAATAAGGTACTAGT | 54542 |
rs2596702 | snp | A/T | 0.482083 | 0.0929373 | | | GRCh38.p7 | 9:122886735 | caaaatcacagggac[A/T]tacttgtttataccc | 54542 |
rs2596703 | snp | A/T | 0.483995 | 0.0880135 | | | GRCh38.p7 | 9:122879571 | CAAGATACCCTCTAA[A/T]CTCTTGGTGTGCTAT | 54542 |
rs2596704 | snp | C/T | 0.466927 | 0.124269 | | | GRCh38.p7 | 9:122885088 | gaactacaaattgta[C/T]atagtactgtattgt | 54542 |
rs2792990 | snp | C/G | 0.4862 | 0.0819127 | intron-variant | RC3H2 | GRCh38.p7 | 9:122859331 | AACTCCTGGGCTCAA[C/G]TGATTCTCCTGGGCC | 54542 |
rs2792991 | snp | C/G | 0.0532157 | 0.154195 | intron-variant | RC3H2 | GRCh38.p7 | 9:122861359 | GCCGGGTGTGGTGGT[C/G]CATGCCTGTAATCCC | 54542 |
rs2792996 | snp | A/C | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122870413 | AAACAAACAAACAAA[A/C]AAAAAAAAAACAACA | 54542 |
rs2792997 | snp | C/T | 0.0715223 | 0.175059 | intron-variant | RC3H2 | GRCh38.p7 | 9:122877777 | CCTGAATTGGCACTT[C/T]AGATATTCCTTCTGA | 54542 |
rs2792998 | snp | A/G | 0.0279526 | 0.114869 | intron-variant, upstream-variant-2KB | RC3H2, SNORD90 | GRCh38.p7 | 9:122881567 | GCACATAGGGTTAAG[A/G]TATGATACAGGCTAG | 54542 |
rs2792999 | snp | C/T | 0.121369 | 0.214369 | intron-variant | RC3H2 | GRCh38.p7 | 9:122882743 | CAATCTCCTCAACTT[C/T]CCATTTCCTGGTTGT | 54542 |
rs2793001 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | RC3H2 | GRCh38.p7 | 9:122886227 | atccacatgcagcat[A/G]tatcagtatttattc | 54542 |
rs2793002 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | RC3H2 | GRCh38.p7 | 9:122887485 | GCTTCCCTGCTCCCC[A/G]CCCAGCACAAGACtt | 54542 |
rs2793003 | snp | C/T | 0.486529 | 0.0809556 | intron-variant | RC3H2 | GRCh38.p7 | 9:122893767 | TCCCCAAAGCACTTA[C/T]CACCTTTTTACTATA | 54542 |
rs2793004 | snp | C/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122894613 | ggctgggcacggttg[C/G]tcacgcctataatcc | 54542 |
rs2793005 | snp | C/T | 0.0137711 | 0.0818286 | intron-variant | RC3H2 | GRCh38.p7 | 9:122897241 | CAAAAATAGTGATTA[C/T]TTTTGCACCAACCTA | 54542 |
rs2793006 | snp | G/T | 0.0535932 | 0.154675 | intron-variant | RC3H2 | GRCh38.p7 | 9:122898775 | AAAAAAGTTCCATAA[G/T]TTTAGTAAAGTAAAA | 54542 |
rs2793007 | snp | C/G | 0.483199 | 0.0901004 | intron-variant | RC3H2 | GRCh38.p7 | 9:122902603 | TAATCCCAGCACTTT[C/G]GGAGGCGGAGGCGGG | 54542 |
rs3049156 | in-del | -/AA | 0.245277 | 0.249955 | intron-variant | RC3H2 | GRCh38.p7 | 9:122849851 | AATGACATTAAAAAC[-/AA]ATTAGCTTTAAGTGC | 54542 |
rs3049159 | in-del | -/TTT | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122860423 | ttttttttttttttt[-/TTT]gagacagggtgtcac | 54542 |
rs3049187 | in-del | -/TTATAAA | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122903114 | TCTAGAATATTTAAA[-/TTATAAA]GTAATACTTAGAACT | 54542 |
rs3860992 | snp | A/C/G | 0.153974 | 0.240485 | intron-variant | RC3H2 | GRCh38.p7 | 9:122853191 | GAAGGCAGCATGCTC[A/C/G]TTAAGAGTCATCACC | 54542 |
rs4292762 | snp | A/G | 0.446902 | 0.154045 | intron-variant | RC3H2 | GRCh38.p7 | 9:122897790 | GTGTTCCTTTCAACT[A/G]AACTGTATTTATATT | 54542 |
rs4838018 | snp | C/T | 0.442926 | 0.158996 | intron-variant | RC3H2 | GRCh38.p7 | 9:122850528 | TTGGCTCACTGTCTC[C/T]GCCTCCCGGGTTCAA | 54542 |
rs4838019 | snp | C/G | 0.443598 | 0.158176 | intron-variant | RC3H2 | GRCh38.p7 | 9:122891366 | agcaaattttctaga[C/G]ttgtctatactcgct | 54542 |
rs4838021 | snp | C/T | 0.44651 | 0.154543 | intron-variant | RC3H2 | GRCh38.p7 | 9:122894820 | GGGAGGTGGAGGTTG[C/T]AGTGAGCCGAGATTG | 54542 |
rs5900548 | in-del | -/A | 0.497416 | 0.0358495 | intron-variant | RC3H2 | GRCh38.p7 | 9:122855117 | GACTCTGTCTCAATT[-/A]AAAAAAAAAAAAAAA | 54542 |
rs5900549 | in-del | -/A | 0.0524604 | 0.153226 | intron-variant | RC3H2 | GRCh38.p7 | 9:122857826 | ACACCAAACCACTGC[-/A]AAATATCCAACATAG | 54542 |
rs6151170 | in-del | -/GATAGATAGATA/GATAGATAGATAGATA | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122850458 | ATAGATAGATAGATA[lengthTooLong]ATTTTGAGATGGAGT | 54542 |
rs6478573 | snp | G/T | 0 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122868123 | ggagggaggtggggg[G/T]gtcagccccccgccc | 54542 |
rs6478574 | snp | C/G | 0 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122868482 | tgtgctgtgtccact[C/G]agggttaaatggatt | 54542 |
rs6478575 | snp | A/C | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122868495 | ctcagggttaaatgg[A/C]ttaagggcggtgcaa | 54542 |
rs6478576 | snp | C/T | 0.454904 | 0.143228 | intron-variant | RC3H2 | GRCh38.p7 | 9:122872329 | TCATTTCCATTGCTA[C/T]AGTCCTACCCGAGCT | 54542 |
rs7026810 | snp | C/T | 0.24932 | 0.249999 | intron-variant | RC3H2 | GRCh38.p7 | 9:122852350 | gcctggcagccaccc[C/T]gtctgggaagtgagg | 54542 |
rs7031473 | snp | A/G | 0.0263992 | 0.111815 | upstream-variant-2KB | RC3H2 | GRCh38.p7 | 9:122906340 | gttagagaccagtct[A/G]gccaacatagtgaaa | 54542 |
rs7033878 | snp | G/T | 0.104728 | 0.20346 | synonymous-codon | RC3H2 | GRCh38.p7 | 9:122855801 | ATTTATACAGGAGCC[G/T]ATGGTGCCACAAGAC | 54542 |
rs7034822 | snp | A/G | 0.089084 | 0.191327 | intron-variant | RC3H2 | GRCh38.p7 | 9:122859529 | CATCTATTGCCACTG[A/G]TTTTGGATTAGTCAG | 54542 |
rs7042013 | snp | A/G | 0.0592355 | 0.161582 | intron-variant | RC3H2 | GRCh38.p7 | 9:122866604 | tgaagacggggtttc[A/G]ctgtgttggctgggc | 54542 |
rs7045905 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | RC3H2 | GRCh38.p7 | 9:122874586 | acagtggtataatct[C/T]agttcacggcagacc | 54542 |
rs7046794 | snp | A/G | 0 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122868027 | ctactgggaagtgag[A/G]agcccctctgcccag | 54542 |
rs7046980 | snp | G/T | 0.170408 | 0.236992 | intron-variant | RC3H2 | GRCh38.p7 | 9:122889085 | TTTCTTCTGAATTTT[G/T]AGACATACCTTATAT | 54542 |
rs7046983 | snp | A/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122867922 | cccgcccagccagcc[A/G]ccccgtccgggaggg | 54542 |
rs7350160 | snp | A/G | 0.43598 | 0.167067 | intron-variant | RC3H2 | GRCh38.p7 | 9:122886225 | tcatccacatgcagc[A/G]tgtatcagtatttat | 54542 |
rs7861476 | snp | A/C | 0.0471551 | 0.14613 | intron-variant | RC3H2 | GRCh38.p7 | 9:122859181 | TTAAATCTAAGGCAG[A/C]CCTTAATGTAGGAAA | 54542 |
rs7869579 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | RC3H2 | GRCh38.p7 | 9:122891140 | ttctcctgcctcagc[C/G]tcccgagtagctggg | 54542 |
rs7872023 | snp | G/T | 0.443598 | 0.158176 | intron-variant | RC3H2 | GRCh38.p7 | 9:122870647 | GCCTTAAATCCTAAA[G/T]GCAAGTGATCCTCCC | 54542 |
rs9776188 | snp | C/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122866379 | CCCctccccctcccc[C/T]ctccctctccccacg | 54542 |
rs9802940 | snp | A/G | 0.269809 | 0.249214 | intron-variant | RC3H2 | GRCh38.p7 | 9:122894076 | catcctggctaacac[A/G]gtgaaaccctgtatc | 54542 |
rs10217201 | snp | A/C | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122896139 | aaaaaaaaaaaaaaa[A/C]tttacgaatttgtgt | 54542 |
rs10217802 | snp | A/G | 0.438386 | 0.164349 | intron-variant | RC3H2 | GRCh38.p7 | 9:122894176 | AGGCAGGAGAATGCC[A/G]TGAACCTGGGAGGCA | 54542 |
rs10540015 | in-del | -/TT | 0.152001 | 0.229992 | intron-variant | RC3H2 | GRCh38.p7 | 9:122860424 | ACCATTTACCCATTC[-/TT]TTTTTTTTTTTTTTT | 54542 |
rs10560103 | in-del | -/T | 0.381308 | 0.21274 | intron-variant | RC3H2 | GRCh38.p7 | 9:122869561 | GGCCAGTTTACACGA[-/T]TTTTTTTTTTTTTTT | 54542 |
rs10561653 | in-del | -/A | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122896121 | AATAGCTGATGAGTT[-/A]AAAAAAAAAAAAAAA | 54542 |
rs10580282 | in-del | -/AG | 0.437259 | 0.165632 | intron-variant | RC3H2 | GRCh38.p7 | 9:122874541 | TTATATTTTTGAGAC[-/AG]AGTCTTGCTCTGCTG | 54542 |
rs10608695 | in-del | -/TTT | 0.228547 | 0.249078 | intron-variant | RC3H2 | GRCh38.p7 | 9:122859272 | TTTTTTTTTTTTTTT[-/TTT]GGTAGAGACAGGGTC | 54542 |
rs10709763 | in-del | -/T | 0 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122868913 | TTTTTTTTTTTTTTT[-/T]GTGGGGGGGTTAAGT | 54542 |
rs10760258 | snp | G/T | 0.452473 | 0.146644 | intron-variant | RC3H2 | GRCh38.p7 | 9:122874183 | AAAAGAAGAGTAAAA[G/T]AAATTTATATAGTAA | 54542 |
rs10818755 | snp | A/C | 0 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122867369 | CTGGGAAGTGAGGAG[A/C]CCCTCTGCCCAGCCA | 54542 |
rs10818757 | snp | A/G | 0 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122887879 | TTCGCGAGTAGCTGA[A/G]ATTATAGGTGCCTGA | 54542 |
rs10818758 | snp | A/G | 0.44333 | 0.158505 | intron-variant | RC3H2 | GRCh38.p7 | 9:122890150 | TGTCTCAAACAAAAC[A/G]AAACAGCAATAACAA | 54542 |
rs10818759 | snp | A/G | 0.327931 | 0.237543 | synonymous-codon | RC3H2 | GRCh38.p7 | 9:122890478 | CTCCACCAGTTGACA[A/G]TTTACAAGTGTCACC | 54542 |
rs10818760 | snp | C/T | 0.443195 | 0.158668 | intron-variant | RC3H2 | GRCh38.p7 | 9:122896840 | CCAGCCTGGCCAACA[C/T]AGTGAAACCCCGTCT | 54542 |
rs10818761 | snp | C/T | 0.442791 | 0.15916 | intron-variant | RC3H2 | GRCh38.p7 | 9:122896907 | GATGTGGGCCTATAG[C/T]CCCAGCTACTTGGGA | 54542 |
rs10985796 | snp | A/G | 0.311369 | 0.242351 | intron-variant | RC3H2 | GRCh38.p7 | 9:122861176 | GGAAAGGATCTTATG[A/G]CTTTCTTAACTCCTT | 54542 |
rs10985797 | snp | A/G | 0.311369 | 0.242351 | intron-variant | RC3H2 | GRCh38.p7 | 9:122861347 | AATACAAAATTAGCC[A/G]GGTGTGGTGGTCCAT | 54542 |
rs10985798 | snp | C/G | 0.0887219 | 0.191022 | intron-variant | RC3H2 | GRCh38.p7 | 9:122862241 | CAAGATCCATGATAA[C/G]GTCAACATTTATCAC | 54542 |
rs10985802 | snp | C/T | 0.089084 | 0.191327 | intron-variant | RC3H2 | GRCh38.p7 | 9:122867590 | AGTGAGAAGCGTCTG[C/T]CCGGCCGCCATCCCA | 54542 |
rs10985803 | snp | A/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122868867 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 54542 |
rs10985804 | snp | C/T | 0.118235 | 0.212457 | intron-variant | RC3H2 | GRCh38.p7 | 9:122873491 | gctgaggtgggcaga[C/T]tgagctcaggagttc | 54542 |
rs10985805 | snp | C/T | 0.438806 | 0.163867 | intron-variant, upstream-variant-2KB | RC3H2, SNORD90 | GRCh38.p7 | 9:122881756 | ccttgactttctggg[C/T]tcaagcaatcctctc | 54542 |
rs10985806 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | RC3H2 | GRCh38.p7 | 9:122883731 | CATGCCTGTAAATCC[C/T]AGCACGTTGAGAGGC | 54542 |
rs10985807 | snp | C/T | 0.089084 | 0.191327 | intron-variant | RC3H2 | GRCh38.p7 | 9:122890097 | agtgagccaagactg[C/T]gccactgcactccag | 54542 |
rs10985809 | snp | C/G | 0.314057 | 0.241654 | intron-variant | RC3H2 | GRCh38.p7 | 9:122898253 | AAACAAAAAAATTGT[C/G]TTAAATATCTTGTAT | 54542 |
rs10985810 | snp | C/G | 0.449473 | 0.150701 | intron-variant | RC3H2 | GRCh38.p7 | 9:122898691 | AAGGCGGAGATTGCA[C/G]TGAGCCGAGATCACG | 54542 |
rs10985812 | snp | A/G | 0.0482946 | 0.147699 | intron-variant | RC3H2 | GRCh38.p7 | 9:122900901 | CTAAATTAAAGGTGG[A/G]ACCATAAACAATTTT | 54542 |
rs10985813 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | RC3H2 | GRCh38.p7 | 9:122902244 | CCAACTTTCTATTTT[A/C]ACAAGTATAACTAAT | 54542 |
rs10985814 | snp | C/T | 0.446249 | 0.154875 | intron-variant | RC3H2 | GRCh38.p7 | 9:122902490 | AACAGTAATATCCGA[C/T]AGAAATATGTGAGCC | 54542 |
rs10985818 | snp | A/T | | | upstream-variant-2KB | RC3H2 | GRCh38.p7 | 9:122907067 | TACATATATGTACAT[A/T]TTTTTTTTTTTGAGA | 54542 |
rs11267855 | in-del | -/ATAGATAG/ATAGATAGATAG/ATAGATAGATAGATAG/ATAGATAGATAGATAGATAG/ATAGATAGATAGATAGATAGATAG | 0.5466 | 0.254274 | intron-variant | RC3H2 | GRCh38.p7 | 9:122850435 | ATATGCTATCTATCT[lengthTooLong]ATAGATAGATAGATA | 54542 |
rs11294543 | in-del | -/T | 0.0543475 | 0.155628 | intron-variant | RC3H2 | GRCh38.p7 | 9:122865902 | CCGAGTTTATATGTA[-/T]TTTTTTTTCCCCTCA | 54542 |
rs11309716 | in-del | -/T | 0.492966 | 0.0588865 | intron-variant | RC3H2 | GRCh38.p7 | 9:122901606 | ACTTCCAATGCATTC[-/T]TTTTTTTTTTTTTTT | 54542 |
rs11311173 | in-del | -/C | 0.0887219 | 0.191022 | intron-variant | RC3H2 | GRCh38.p7 | 9:122888923 | TAAAAGTCTGTACCA[-/C]TTTGCATGCCCATGA | 54542 |
rs11321863 | in-del | -/A | 0 | 0 | intron-variant, upstream-variant-2KB | RC3H2, SNORD90 | GRCh38.p7 | 9:122881476 | GTGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 54542 |
rs11433169 | in-del | -/A/AA/AAA | 0.414905 | 0.187899 | intron-variant | RC3H2 | GRCh38.p7 | 9:122898749 | AAAAAAAAAAAAAAA[-/A/AA/AAA]GTTCCATAAGTTTAG | 54542 |
rs12001002 | snp | C/T | 0.0193772 | 0.0965046 | downstream-variant-500B | RC3H2 | GRCh38.p7 | 9:122849090 | TCTATGGTAAGAACA[C/T]CTAACTCCACTCTTC | 54542 |
rs12004392 | snp | A/C | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122850574 | cagcctcccaggcag[A/C]tgagaatacaggtgc | 54542 |
rs12115466 | snp | A/G | 0.105038 | 0.203681 | intron-variant, downstream-variant-500B | RC3H2 | GRCh38.p7 | 9:122853394 | AAAAAAAAAAAAAAA[A/G]AAAGAAAAATACTGA | 54542 |
rs12216917 | snp | C/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122851856 | tcgctacaacctcca[C/T]ctcccagccgcctgc | 54542 |
rs12338856 | snp | C/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122902621 | aggcggaggcgggag[C/G]tgggtggatcacttg | 54542 |
rs12343935 | snp | A/G | 0.0640965 | 0.167152 | upstream-variant-2KB | RC3H2 | GRCh38.p7 | 9:122906257 | TGACCATGACgccgg[A/G]cgcggtggctgatgc | 54542 |
rs12376593 | snp | G/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122862361 | CCTAGATGACTTTCA[G/T]GATTCTAGGCTCTCC | 54542 |
rs12377337 | snp | A/C/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122899121 | TTTTTTTTTTTTTCA[A/C/G]AGACAGAGTCTCCCT | 54542 |
rs12378760 | snp | C/T | 0.0984431 | 0.198823 | intron-variant | RC3H2 | GRCh38.p7 | 9:122899004 | AGATGTTTAAAAATG[C/T]AGTCACATTCAAAGA | 54542 |
rs12380835 | snp | C/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122894158 | cagttactccagagg[C/T]tgaggcaggagaatg | 54542 |
rs13288262 | snp | C/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122867975 | cccggccagccgccc[C/T]gtccgggaggtgagg | 54542 |
rs13288540 | snp | G/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122867984 | ccgccccgtccggga[G/T]gtgaggggcgcctct | 54542 |
rs13289710 | snp | C/T | 0.00846247 | 0.0644951 | intron-variant | RC3H2 | GRCh38.p7 | 9:122864036 | gccaccgtgcccagc[C/T]TGTAAAAGTCCTTTA | 54542 |
rs13290002 | snp | C/G | 0 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122864034 | gagccaccgtgccca[C/G]ccTGTAAAAGTCCTT | 54542 |
rs13300176 | snp | A/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122862789 | aatcccagctactta[A/G]gaggctgaggcagga | 54542 |
rs16912287 | snp | G/T | 0.0652144 | 0.168387 | intron-variant | RC3H2 | GRCh38.p7 | 9:122883523 | AAGAGGACATCACAC[G/T]TACATAATTTAAAAA | 54542 |
rs16912290 | snp | C/T | 0.021333 | 0.101051 | intron-variant | RC3H2 | GRCh38.p7 | 9:122887308 | AATCCTTTGGAGTCA[C/T]TCATTATGATGTTTA | 54542 |
rs16912294 | snp | A/G | 0.021333 | 0.101051 | intron-variant | RC3H2 | GRCh38.p7 | 9:122891811 | TATATTCAATCATTC[A/G]ACAATTGTTTATTAT | 54542 |
rs16912312 | snp | A/G | 0.312837 | 0.241974 | upstream-variant-2KB | RC3H2 | GRCh38.p7 | 9:122905517 | CGATCACGTGACAAG[A/G]GAGCCCCGGAGCACT | 54542 |
rs17220841 | snp | C/T | 0.0386986 | 0.13361 | intron-variant | RC3H2 | GRCh38.p7 | 9:122883192 | GTCTTTACATAGATA[C/T]TTACTGCTTACCTTA | 54542 |
rs17220848 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | RC3H2 | GRCh38.p7 | 9:122888239 | AAAAGTCAAAACACT[A/G]TGTTCTAAAGTAACC | 54542 |
rs28565986 | snp | A/C | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122870409 | AAACAAACAAACAAA[A/C]AAACAAAAAAAAAAC | 54542 |
rs28750180 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RC3H2 | GRCh38.p7 | 9:122878357 | CTGCAAGCTCCACTT[A/C]CCGGGTTCAGGCCAT | 54542 |
rs34042219 | in-del | -/C | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122890098 | TGAGCCAAGACTGCG[-/C]CCACTGCACTCCAGC | 54542 |
rs34182984 | in-del | -/C | | | intron-variant, downstream-variant-500B | RC3H2, SNORD90 | GRCh38.p7 | 9:122879983 | GCAACTGAGCATATT[-/C]CCCACATACCTGGAT | 54542 |
rs34237757 | in-del | -/AA | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122896137 | AAAAAAAAAAAAAAA[-/AA]CTTTACGAATTTGTG | 54542 |
rs34337035 | in-del | -/AC | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122864356 | GGAAATCTTATGCTG[-/AC]ACTCAGTAACAATTA | 54542 |
rs34377701 | in-del | -/G/GG | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122871506 | TTTCACCGTGTTAGT[-/G/GG]GGGGGGGGGGGTTTC | 54542 |
rs34602294 | in-del | -/ATAT | 0.0193772 | 0.0965046 | upstream-variant-2KB | RC3H2 | GRCh38.p7 | 9:122907000 | TAAATATATATACAC[-/ATAT]ATAGATACATATAAG | 54542 |
rs34619127 | in-del | -/A | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122858343 | TATGTGGTGATACTG[-/A]AAAAAGGTCCTAACC | 54542 |
rs34712728 | in-del | -/G | | | upstream-variant-2KB | RC3H2 | GRCh38.p7 | 9:122906254 | AATGACCATGACGCC[-/G]GGGCGCGGTGGCTGA | 54542 |
rs34730534 | in-del | -/A | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122864883 | CATGCCTCAGCCTCC[-/A]AAAGTGCTGGGATTA | 54542 |
rs34777089 | in-del | -/C | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122894205 | AGAGCTTGCAGTGAG[-/C]CCGAGATCGCGCCAC | 54542 |
rs34808235 | snp | G/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122887762 | TTTTTTTTTTTTTTT[G/T]GAGATGGAGTTTTGC | 54542 |
rs34883365 | snp | A/C/G | 0.00950277 | 0.068273 | synonymous-codon, missense | RC3H2 | GRCh38.p7 | 9:122857932 | TCTTACATCCGCACG[A/C/G]AAGTCTACACTGAAC | 54542 |
rs35020439 | in-del | -/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122872128 | CTTCAAACATCATTA[-/T]GGCCAAGAGAACCAC | 54542 |
rs35177694 | snp | C/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122892303 | TTTTTAGTAGAGATG[C/G]GCTTTCGCCTTGTTG | 54542 |
rs35436946 | in-del | -/G | 0.291235 | 0.246576 | intron-variant | RC3H2 | GRCh38.p7 | 9:122871507 | TTTCACCGTGTTAGT[-/G]GGGGGGGGGGTTTCA | 54542 |
rs35483395 | in-del | -/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122896047 | GGTGTCTTTTGGCTT[-/T]CCGTGGGCCATACTG | 54542 |
rs35654374 | in-del | -/CT | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122864359 | AATCTTATGCTGACA[-/CT]CAGTAACAATTAATG | 54542 |
rs35675000 | in-del | -/ACA | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122854427 | TGTTATATAGCTCAG[-/ACA]ACAAGCAAAGCACAT | 54542 |
rs35775529 | in-del | -/C | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122890023 | GCGTGTGCCTGTAGT[-/C]CCCAGCTACTTAGGG | 54542 |
rs35829216 | in-del | -/C | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122892305 | TTTAGTAGAGATGGG[-/C]TTTCGCCTTGTTGCC | 54542 |
rs35848690 | snp | C/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122890961 | TGTTATTTCATCCAT[C/T]TAAAATACAAATATT | 54542 |
rs35911562 | in-del | -/A | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122850277 | ACCACTCCTGGCTTG[-/A]AAAGTCCTGTTTTCC | 54542 |
rs35932213 | in-del | -/T | 0.439085 | 0.163545 | intron-variant | RC3H2 | GRCh38.p7 | 9:122890724 | TAGTAATAAGAAGCC[-/T]AATTTTTAGCTACTT | 54542 |
rs36023960 | in-del | -/A | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122889184 | TTTTCATTTGCTTAT[-/A]AATTTTTTTGTGATG | 54542 |
rs36205979 | in-del | -/TGTGTGTGTGTGTGTGTGTGTG | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122868840 | ATATTCCCTCCTATA[-/TGTGTGTGTGTGTGTGTGTGTG]TGTGTGTGTGTGTGT | 54542 |
rs41277130 | snp | C/G | 0.0412454 | 0.137556 | intron-variant | RC3H2 | GRCh38.p7 | 9:122854099 | GGCCTATATGAGGAG[C/G]GAAAAAAAGAAAAGT | 54542 |
rs41277132 | snp | C/T | 0.0412488 | 0.137561 | intron-variant | RC3H2 | GRCh38.p7 | 9:122854126 | AAGTTAGCTTCCAAC[C/T]ATAGCTTTCAACTGT | 54542 |
rs41277134 | snp | A/G | | | intron-variant, downstream-variant-500B | RC3H2, SNORD90 | GRCh38.p7 | 9:122879895 | TAAGCCACCAAGGGC[A/G]TGGGGGTTGGGGGGG | 54542 |
rs41296053 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | RC3H2 | GRCh38.p7 | 9:122898111 | TGACAAGACTTGGCT[A/T]GGAAGCAAAATGAGG | 54542 |
rs41304848 | snp | C/T | 0.0744748 | 0.178019 | intron-variant | RC3H2 | GRCh38.p7 | 9:122898104 | AAATCTCTGACAAGA[C/T]TTGGCTAGGAAGCAA | 54542 |
rs55684376 | snp | C/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122886223 | GCTCATCCACATGCA[C/G]CATGTATCAGTATTT | 54542 |
rs55892544 | in-del | -/AGCCAGCCGCCCCGTCCGGGAGGGAGGTGGGGGGGTCAGCCCCCCGCCC | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122867914 | GTCAGCCCCCCGCCC[lengthTooLong]GGCCAGCCGCCCCGT | 54542 |
rs56014311 | snp | A/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122886074 | TTTCTATTTTCAGTA[A/G]AGACAGAGTTTTCCC | 54542 |
rs56129356 | snp | A/T | 0.0193772 | 0.0965046 | intron-variant | RC3H2 | GRCh38.p7 | 9:122858186 | CAGTTTATGATATTG[A/T]TGGGATAAAAAAATA | 54542 |
rs56240814 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | RC3H2 | GRCh38.p7 | 9:122888095 | TCTGGTGGCATTAAC[A/G]TAATTATTTGCTTGC | 54542 |
rs56326911 | in-del | -/G | | | upstream-variant-2KB | RC3H2 | GRCh38.p7 | 9:122905881 | CAAAGAGTCCAAAGT[-/G]GGGGGGGGAGGGGGG | 54542 |
rs56340543 | snp | A/C | 0.00394334 | 0.0442281 | intron-variant | RC3H2 | GRCh38.p7 | 9:122875305 | GAGCTCATTATGTAC[A/C]GTGCCCAAGCTAGCC | 54542 |
rs56346835 | in-del | -/A | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122902866 | AAAAAAAAAAAAAAA[-/A]GTTAAAATAGCTAAA | 54542 |
rs56682781 | snp | G/T | | | intron-variant, upstream-variant-2KB | RC3H2, SNORD90 | GRCh38.p7 | 9:122881971 | CCACATGATAATTAA[G/T]AAATTTTCTAGGGAG | 54542 |
rs56981916 | snp | C/G | 0.0655868 | 0.168795 | intron-variant | RC3H2 | GRCh38.p7 | 9:122879389 | ACAGAGTGAGACTTT[C/G]TCTAAAAAAAAAAGA | 54542 |
rs57140227 | snp | C/T | 0.482979 | 0.0906686 | intron-variant | RC3H2 | GRCh38.p7 | 9:122852338 | AGGAGCCTCTCTGCC[C/T]GGCAGCCACCCCGTC | 54542 |
rs57461070 | in-del | -/AA/AAA | | | intron-variant, downstream-variant-500B | RC3H2 | GRCh38.p7 | 9:122853397 | AAAAAAAAAAAAAAA[-/AA/AAA]GAAAAATACTGATTT | 54542 |
rs57782881 | in-del | -/CTCA | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122864359 | AATCTTATGCTGACA[-/CTCA]GTAACAATTAATGGT | 54542 |
rs57985244 | in-del | -/A/AAAAGA | 0 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122861515 | AGAAAAGAAAAAAAA[-/A/AAAAGA]CCATATATATATGGC | 54542 |
rs58012568 | snp | A/G | 0.467234 | 0.12373 | intron-variant | RC3H2 | GRCh38.p7 | 9:122852114 | TCTGCCCGGCCGCCC[A/G]TCGTCTGGGATGTGG | 54542 |
rs58033377 | in-del | -/T | 0 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122869581 | TTTTTTTTTTTTTTT[-/T]GAGGCGGAGTTTTGC | 54542 |
rs58296361 | snp | G/T | | | upstream-variant-2KB | RC3H2 | GRCh38.p7 | 9:122906741 | AAAAATCAGTGTTTT[G/T]GAAAAAAGATTCATT | 54542 |
rs58937243 | snp | A/G | | | upstream-variant-2KB | RC3H2 | GRCh38.p7 | 9:122906742 | AAAATCAGTGTTTTT[A/G]AAAAAAGATTCATTG | 54542 |
rs59033438 | snp | A/T | 0.0182019 | 0.0936463 | intron-variant | RC3H2 | GRCh38.p7 | 9:122901263 | AGGAATATAAGCTAC[A/T]GAAATGGACTGTCAC | 54542 |
rs59761449 | in-del | -/TA | | | upstream-variant-2KB | RC3H2 | GRCh38.p7 | 9:122906938 | GTATATATATATATA[-/TA]CACACATATATACAT | 54542 |
rs60422514 | in-del | -/GG | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122871517 | TAGTGGGGGGGGGGG[-/GG]TTTCATCGTGTTAGC | 54542 |
rs60753674 | snp | C/T | 0.435694 | 0.167385 | intron-variant | RC3H2 | GRCh38.p7 | 9:122887102 | TTTCCCCAGTAACCT[C/T]TCGTCTAATGGGTTT | 54542 |
rs61167274 | snp | G/T | 0.442926 | 0.158996 | intron-variant | RC3H2 | GRCh38.p7 | 9:122884220 | ATGGCATGAACCTGG[G/T]AGGTGGAGCTTGCAG | 54542 |
rs62580883 | snp | C/T | 0.105924 | 0.204309 | intron-variant | RC3H2 | GRCh38.p7 | 9:122852521 | GCCAGCCGCCCCGTC[C/T]GGGAGGGAGGTGGGG | 54542 |
rs62580884 | snp | A/C | 0.0887219 | 0.191022 | intron-variant | RC3H2 | GRCh38.p7 | 9:122857459 | AAGAAATACCTCAGA[A/C]AGCCCAGGATTCATA | 54542 |
rs62580915 | snp | A/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122867222 | CAGCCACCCCGTCCG[A/G]GAGGGAGGTGGGGGG | 54542 |
rs62580917 | snp | C/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122868179 | AGGGGCGCCTCTGCC[C/T]GGCCGCCCCTACTGG | 54542 |
rs62580918 | snp | C/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122868183 | GCGCCTCTGCCCGGC[C/T]GCCCCTACTGGGAAG | 54542 |
rs62580919 | snp | A/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122868195 | GGCCGCCCCTACTGG[A/G]AAGTGAGGAGCCCCT | 54542 |
rs62580920 | snp | A/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122868203 | CTACTGGGAAGTGAG[A/G]AGCCCCTCTGCCCGG | 54542 |
rs62580921 | snp | C/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122868209 | GGAAGTGAGGAGCCC[C/G]TCTGCCCGGCCACCA | 54542 |
rs62580922 | snp | C/T | 0.0887219 | 0.191022 | intron-variant | RC3H2 | GRCh38.p7 | 9:122869315 | GTTATTAATGTTATA[C/T]ATAAACATATGGTAA | 54542 |
rs62580923 | snp | A/T | 0.0962929 | 0.197165 | intron-variant | RC3H2 | GRCh38.p7 | 9:122873038 | TGTTTACATATAATA[A/T]ATATGTATTCTAAGA | 54542 |
rs62580926 | snp | A/G | 0.5 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122893046 | AAAAAAAAAAAAAAG[A/G]AATATTGCAGAAATA | 54542 |
rs62580927 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RC3H2 | GRCh38.p7 | 9:122895365 | TAGAGATGGGGTTTC[A/G]CCATGTTGTCCAGGC | 54542 |
rs63268662 | snp | A/T | 0.5 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122855117 | GACTCTGTCTCAATT[A/T]AAAAAAAAAAAAAAA | 54542 |
rs68013227 | in-del | -/GTGTGTGTGTGTGTGTGTGTGT | 0 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122868869 | TGTGTGTGTGTGTGT[-/GTGTGTGTGTGTGTGTGTGTGT]ATGTGTTTTTTTTTT | 54542 |
rs71388328 | in-del | -/G | 0 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122899382 | GCGTGAGCCACCGCG[-/G]CCCGGCCCTGCGCTT | 54542 |
rs71508186 | in-del | -/C | 0.5 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122899388 | GCCACCGCGGCCCGG[-/C]CCTGCGCTTTTATAT | 54542 |
rs71511545 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RC3H2 | GRCh38.p7 | 9:122871116 | AATTCCAGTAACCTT[C/T]CTGCACCTGTAGCCA | 54542 |
rs71511546 | snp | C/T | 0.5 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122874777 | CTCCTGCCTTTGCCT[C/T]CCAAACTGCTGGGAA | 54542 |
rs71511547 | snp | C/T | 0.271162 | 0.249103 | intron-variant | RC3H2 | GRCh38.p7 | 9:122887570 | GGGAAATGGTATATA[C/T]GAAAGCCCATAATCT | 54542 |
rs71936774 | in-del | -/TAAATTA | 0.236724 | 0.249647 | intron-variant | RC3H2 | GRCh38.p7 | 9:122903110 | CAACTCTAGAATATT[-/TAAATTA]TAAAGTAATACTTAG | 54542 |
rs72033785 | in-del | -/AAA | | | intron-variant, downstream-variant-500B | RC3H2 | GRCh38.p7 | 9:122853379 | AAAAAAAAAAAAAAA[-/AAA]AAGAAAAATACTGAT | 54542 |
rs72167284 | in-del | -/AAA | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122896121 | AATAGCTGATGAGTT[-/AAA]AAAAAAAAAAAAAAA | 54542 |
rs72530837 | in-del | -/A | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122870423 | CAAACAAAAAAAAAA[-/A]CAACAAACTGAGATA | 54542 |
rs72753236 | snp | C/T | | | missense | RC3H2 | GRCh38.p7 | 9:122858866 | AGATGCGCCTGCTGT[C/T]GTACACAGGAGCATA | 54542 |
rs72753237 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RC3H2 | GRCh38.p7 | 9:122859188 | TAAGGCAGCCCTTAA[C/T]GTAGGAAAATATAAT | 54542 |
rs72753244 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RC3H2 | GRCh38.p7 | 9:122897097 | GCTGATGAGCTAAAA[A/G]CATAAACATAAATCA | 54542 |
rs72753245 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RC3H2 | GRCh38.p7 | 9:122899030 | AAAGAGAAAAAATAT[A/G]TAACAGAAAGTATTC | 54542 |
rs72753246 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RC3H2 | GRCh38.p7 | 9:122903809 | ATGTAACGACCTCTA[C/T]TTCTTCAAAAATTGA | 54542 |
rs72753247 | snp | A/G | 0.00914312 | 0.0669923 | upstream-variant-2KB | RC3H2 | GRCh38.p7 | 9:122906875 | CAGTAATTTCAACTG[A/G]ACAGTGATAGGTAAT | 54542 |
rs73664141 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | RC3H2 | GRCh38.p7 | 9:122905889 | CCAAAGTGGGGGGGG[A/G]AGGGGGGGAAGAAAG | 54542 |
rs74362912 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RC3H2 | GRCh38.p7 | 9:122862024 | TATTCCAGGCACTGT[A/G]CTTTACATAAATTAT | 54542 |
rs74369362 | snp | A/T | 0.5 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122871944 | ACCATGCCCAGCCAA[A/T]TTTTTTTTTTTGTAG | 54542 |
rs74391969 | in-del | -/TG | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122860425 | TTTTTTTTTTTTTTT[-/TG]AGACAGGGTGTCACT | 54542 |
rs74404492 | snp | A/G | 0.030278 | 0.119257 | intron-variant | RC3H2 | GRCh38.p7 | 9:122901503 | TAACGTGTGAAGTAT[A/G]TATGACTCAAATTTT | 54542 |
rs74426418 | snp | A/G | 0.0114858 | 0.0749063 | intron-variant | RC3H2 | GRCh38.p7 | 9:122865330 | GAATTTCCAGTAATC[A/G]TTTTTACCTAATACC | 54542 |
rs74555175 | in-del | -/T/TCCCCCT | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122866379 | CCCTCCCCCTCCCCC[-/T/TCCCCCT]CTCCCTCTCCCCACG | 54542 |
rs74580336 | snp | A/C | 0 | 0 | intron-variant, upstream-variant-2KB | RC3H2, SNORD90 | GRCh38.p7 | 9:122881460 | GAGACTCCGTCTCAA[A/C]AAAAAAAAAAAAAAA | 54542 |
rs74717209 | snp | G/T | 0.5 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122901947 | TTTTTTTTTTTTTTT[G/T]AGACGGAGTTTCGCT | 54542 |
rs74759344 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | RC3H2 | GRCh38.p7 | 9:122902471 | AAGAGTAATGCTGAT[C/T]TACAACAGTAATATC | 54542 |
rs74885279 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | RC3H2 | GRCh38.p7 | 9:122877343 | ACTGCTGGGACTACA[C/G]GCATGAGCTATGGTG | 54542 |
rs74896876 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | RC3H2 | GRCh38.p7 | 9:122877670 | AGAACTTTATAATTA[C/T]ACCTTTAATTCTTTT | 54542 |
rs74938199 | snp | A/T | 0.078151 | 0.181571 | intron-variant | RC3H2 | GRCh38.p7 | 9:122902252 | CTATTTTAACAAGTA[A/T]AACTAATATTAGTGA | 54542 |
rs74947025 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RC3H2 | GRCh38.p7 | 9:122897888 | TTAACTTTCCATATT[C/T]CATTTTTAGGAACAC | 54542 |
rs75062370 | snp | C/T | 0 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122867557 | AGGAGCCCCTCTGCC[C/T]GGCTGCCCAGTCTGG | 54542 |
rs75069876 | snp | A/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122887519 | ACCCTAGACTGGAGT[A/T]AGGCATTTACCCAAA | 54542 |
rs75275597 | snp | A/C | 0.5 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122876627 | AGCAAGACTCCACCT[A/C]AAAAAAAAAAAAAAA | 54542 |
rs75305840 | snp | G/T | 0.5 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122891036 | TTTTTTTTTTTTTTT[G/T]GGAGACAGAGTCTCA | 54542 |
rs75339039 | snp | A/G | 0.030278 | 0.119257 | intron-variant | RC3H2 | GRCh38.p7 | 9:122896335 | TTATATAAAAAGTCA[A/G]GTGAAGTAAAAAAAA | 54542 |
rs75352167 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | RC3H2 | GRCh38.p7 | 9:122903980 | TTAACCATTAAAAGG[C/T]TGCACTGGCTAACAT | 54542 |
rs75461841 | snp | C/G | 0.046775 | 0.145601 | intron-variant | RC3H2 | GRCh38.p7 | 9:122886323 | ATGGACATTCGGATT[C/G]TTTCCACCTTTTGAC | 54542 |
rs75474525 | snp | A/G | 0 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122855132 | AAAAAAAAAAAAAAA[A/G]AAGGCATAGTGCTTA | 54542 |
rs75537080 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RC3H2 | GRCh38.p7 | 9:122888855 | AGTGGGATTGCTAGA[C/T]CAAAGGGTAAACACA | 54542 |
rs75568698 | snp | C/T | 0 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122867518 | AGGGGCGCCTCTGCC[C/T]GGCCGCCTATCGTCT | 54542 |
rs75782312 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | RC3H2 | GRCh38.p7 | 9:122882402 | AGTGTTCTGCCAAAG[A/C]AACATTTTTCTGTCT | 54542 |
rs75784325 | snp | C/G | 0.0648419 | 0.167978 | intron-variant | RC3H2 | GRCh38.p7 | 9:122873148 | TTTAAGTTGAACAAA[C/G]ATTTGCTGAATTTCT | 54542 |
rs75844899 | snp | A/C | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122875311 | ATTATGTACAGTGCC[A/C]AAGCTAGCCACTGAG | 54542 |
rs75926281 | snp | G/T | 0.5 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122871316 | TTCTTTTTTTTTTTT[G/T]AGACGGAGTCTCGCT | 54542 |
rs75934340 | in-del | -/AA | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122894270 | TCTCAAAAAAAAAAA[-/AA]GTTCAATGCAATTCA | 54542 |
rs75938130 | snp | A/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122873473 | ATCCTAGCACTTTGG[A/G]AGGCTGAGGTGGGCA | 54542 |
rs75969785 | snp | A/C | 0.5 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122894258 | AGCAAGACTCCGTCT[A/C]AAAAAAAAAAAAAGT | 54542 |
rs76198507 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | RC3H2 | GRCh38.p7 | 9:122856629 | TTATGCAGTATCAAA[A/G]AACAAAAGGAATTCA | 54542 |
rs76426085 | snp | A/C | 0.5 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122884851 | AGCGAAAGTCCGTCT[A/C]CAAAAAAAAAAAAAA | 54542 |
rs76598291 | snp | G/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122887517 | CTACCCTAGACTGGA[G/T]TAAGGCATTTACCCA | 54542 |
rs76706859 | in-del | -/CACT | 0.26818 | 0.249338 | intron-variant | RC3H2 | GRCh38.p7 | 9:122864357 | GAAATCTTATGCTGA[-/CACT]CAGTAACAATTAATG | 54542 |
rs76760394 | snp | A/G | 0 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122867238 | gagggaggtgggggg[A/G]tcagccccccgcccg | 54542 |
rs76852352 | snp | G/T | 0.5 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122871315 | CTTCTTTTTTTTTTT[G/T]GAGACGGAGTCTCGC | 54542 |
rs76912315 | snp | A/C | 0 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122884853 | CGAAAGTCCGTCTCC[A/C]AAAAAAAAAAAAAAG | 54542 |
rs77033428 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RC3H2 | GRCh38.p7 | 9:122861760 | AGAAAAAGGTATATG[A/G]GCTGCCTTTAAGTTT | 54542 |
rs77073169 | snp | A/C | 0 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122894259 | GCAAGACTCCGTCTC[A/C]AAAAAAAAAAAAGTT | 54542 |
rs77090412 | snp | A/C | 0.5 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122854448 | AGCAAAGCACATTTC[A/C]TGAACTGGGGGTAGA | 54542 |
rs77265444 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | RC3H2 | GRCh38.p7 | 9:122862115 | AAACTCATAGACTTA[C/T]CAACAAAAAGGCAAC | 54542 |
rs77413044 | snp | A/C | 0.0599851 | 0.162463 | intron-variant | RC3H2 | GRCh38.p7 | 9:122892056 | TATTCTGTTACAGCA[A/C]TATTACACAGTGAAT | 54542 |
rs77427086 | in-del | -/GTT | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122875479 | GCATTGTCTGTGGCT[-/GTT]GTTTTTTTGCTACAG | 54542 |
rs77459166 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | RC3H2 | GRCh38.p7 | 9:122889636 | TTATCCCCTAAAAAC[C/G]ATCAAGAGTTTAAAC | 54542 |
rs77557497 | snp | A/C | 0.5 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122876629 | CAAGACTCCACCTCA[A/C]AAAAAAAAAAAAAGT | 54542 |
rs77579008 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | RC3H2 | GRCh38.p7 | 9:122901194 | AAAAATGTAAACCTT[A/G]GGGCTTAGTTCTTCT | 54542 |
rs77596117 | snp | A/T | 0.0505692 | 0.150756 | intron-variant | RC3H2 | GRCh38.p7 | 9:122886991 | TAAAAGTAGATTTTT[A/T]AAATATCTTAAAACT | 54542 |
rs78325050 | snp | A/C | | | downstream-variant-500B | RC3H2 | GRCh38.p7 | 9:122849362 | ACTCATAAAAAGCTG[A/C]TTGAAGCTTAAGTTA | 54542 |
rs78365758 | snp | G/T | 0.000657815 | 0.0181239 | utr-variant-5-prime | RC3H2 | GRCh38.p7 | 9:122897557 | GCAGATCATTATTTT[G/T]CTGTGTAGTGTTTTG | 54542 |
rs78372719 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | RC3H2 | GRCh38.p7 | 9:122860369 | AAAAACGATTCCCAG[A/T]TATTAACGTGATTCA | 54542 |
rs78398821 | snp | C/T | 0.0648419 | 0.167978 | intron-variant | RC3H2 | GRCh38.p7 | 9:122877785 | GGCACTTCAGATATT[C/T]CTTCTGAAGATTATT | 54542 |
rs78423447 | snp | A/C/T | 0 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122867538 | GCCTATCGTCTGGGA[A/C/T]GTGAGGAGCCCCTCT | 54542 |
rs78450930 | snp | A/T | 0.0494327 | 0.149241 | intron-variant | RC3H2 | GRCh38.p7 | 9:122856019 | ACTAATATAAAAAAC[A/T]GTAATAAGCAAGAAA | 54542 |
rs78458626 | snp | A/C | 0.5 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122902851 | GAGAGACTGTCTCAA[A/C]AAAAAAAAAAAAAAA | 54542 |
rs78635967 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | RC3H2 | GRCh38.p7 | 9:122862593 | TAAAAATTTAGATTT[A/T]TTTTTTAAAAGTCTT | 54542 |
rs78703653 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | RC3H2 | GRCh38.p7 | 9:122864068 | TAAACAATCTCCCCC[A/G]TCATGTGCTGACTGC | 54542 |
rs78781772 | snp | A/G | 0.5 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122893044 | TAAAAAAAAAAAAAA[A/G]GGAATATTGCAGAAA | 54542 |
rs78926480 | snp | C/T | 0.0119306 | 0.0763085 | missense | RC3H2 | GRCh38.p7 | 9:122897437 | TGATGGGTTTGTGCA[C/T]ATTCTCATCAAATTC | 54542 |
rs78980512 | snp | A/G | 0.5 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122856178 | ATGGGGTGCACCAAG[A/G]AAAAAAAAAGTAAGA | 54542 |
rs79107864 | snp | A/C | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122887516 | CCTACCCTAGACTGG[A/C]GTAAGGCATTTACCC | 54542 |
rs79170821 | snp | A/G | 0.030278 | 0.119257 | intron-variant | RC3H2 | GRCh38.p7 | 9:122871924 | CACCCAGGCAGGAGT[A/G]AGTCACCATGCCCAG | 54542 |
rs79179553 | snp | A/G | 0 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122867536 | CCGCCTATCGTCTGG[A/G]ACGTGAGGAGCCCCT | 54542 |
rs79330216 | snp | A/C | 0.0648419 | 0.167978 | intron-variant | RC3H2 | GRCh38.p7 | 9:122901460 | GAATTGCAATTTAAA[A/C]GACTGCTATAATATG | 54542 |
rs79330329 | snp | C/T | 0.0652144 | 0.168387 | intron-variant | RC3H2 | GRCh38.p7 | 9:122869955 | TTCAGGAAGACAATC[C/T]GGTTGTCTGGAGGGG | 54542 |
rs79336029 | in-del | -/GG | | | upstream-variant-2KB | RC3H2 | GRCh38.p7 | 9:122905888 | TCCAAAGTGGGGGGG[-/GG]AGGGGGGGAAGAAAG | 54542 |
rs79344833 | snp | C/T | 0.0592355 | 0.161582 | intron-variant | RC3H2 | GRCh38.p7 | 9:122901576 | TATTAGATATAACTT[C/T]CAATGCATTCTTTTT | 54542 |
rs79580130 | snp | C/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122860462 | ACCCGGGCTGGAGTG[C/G]ACTGACATAATCACA | 54542 |
rs79743659 | in-del | -/AAAAAA | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122896133 | GTTAAAAAAAAAAAA[-/AAAAAA]CTTTACGAATTTGTG | 54542 |
rs79828468 | snp | C/G/T | 0.0110115 | 0.0733791 | intron-variant | RC3H2 | GRCh38.p7 | 9:122851266 | CCTTCAGTATGAAAG[C/G/T]ATTTTATAAATTTTC | 54542 |
rs79832342 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | RC3H2 | GRCh38.p7 | 9:122860368 | TAAAAACGATTCCCA[C/G]ATATTAACGTGATTC | 54542 |
rs79841101 | snp | A/G/T | 1.66457e-05 | 0.00288489 | missense | RC3H2 | GRCh38.p7 | 9:122854199 | CCTGCTGAAGTTCAA[A/G/T]GCTCAAAAGGTCCCC | 54542 |
rs79929537 | in-del | -/C | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122895995 | TGTTCTTTTTTTTTT[-/C]CCCCCTAATGTTCAA | 54542 |
rs80042045 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | RC3H2 | GRCh38.p7 | 9:122887145 | TAATTCTTGCTGAAG[C/T]CCATTAATACATTTG | 54542 |
rs80070393 | snp | C/G/T | 0.00199481 | 0.0315187 | intron-variant | RC3H2 | GRCh38.p7 | 9:122874610 | GCAGACCTGACCTCC[C/G/T]GAGTTCAAGCAATCC | 54542 |
rs80093421 | snp | A/C | 0.0944473 | 0.199431 | intron-variant | RC3H2 | GRCh38.p7 | 9:122865088 | GAAAAAAAAACAATT[A/C]TGGTCCAGTCTCTTT | 54542 |
rs80286309 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | RC3H2 | GRCh38.p7 | 9:122896567 | CTAAAGAAAATCTTT[C/T]GCAGAATACAATCAT | 54542 |
rs111337541 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RC3H2 | GRCh38.p7 | 9:122887868 | CGTGCCTCAGCTTCG[C/T]GAGTAGCTGAGATTA | 54542 |
rs111358831 | snp | C/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122852581 | CGTCCGGGAGGGAGG[C/T]GTGGGGGTCAGCCCC | 54542 |
rs111378936 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RC3H2 | GRCh38.p7 | 9:122860231 | TTCTGAAACCACTAA[G/T]AGAAAACACTTCAGA | 54542 |
rs111436987 | snp | A/G | 0.5 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122888804 | AACTGTATGCATTCT[A/G]TACCTTCTGTTGTCT | 54542 |
rs111451604 | snp | C/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122902036 | CCGGGTTCAAGCGAT[C/T]CTCCTGCCTCAGCCT | 54542 |
rs111454655 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | RC3H2, SNORD90 | GRCh38.p7 | 9:122881734 | GCACAATCTAGGCTC[A/G]CTGTAGCCTTGACTT | 54542 |
rs111485875 | snp | A/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122903115 | CTAGAATATTTAAAT[A/T]ATAAAGTAATACTTA | 54542 |
rs111533465 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RC3H2 | GRCh38.p7 | 9:122858341 | TGTATGTGGTGATAC[C/T]GAAAAAAGGTCCTAA | 54542 |
rs111585362 | snp | A/C | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122867306 | GCCCCCCGCCCGGCC[A/C]GCCGCCCCGTCCGGG | 54542 |
rs111625772 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | RC3H2 | GRCh38.p7 | 9:122851632 | CTGCAGAGTGCCTGC[A/G/T]ATTGCAGGCGCGCGC | 54542 |
rs111674006 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RC3H2 | GRCh38.p7 | 9:122875702 | TAGACAAAGGAAAGG[A/T]CTCAAAGGCAAGGCT | 54542 |
rs111683415 | snp | C/T | 0.5 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122893151 | GATAATACATGAAAG[C/T]CATTTAAGTAAAATT | 54542 |
rs111690729 | snp | C/T | 0.5 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122899378 | TGCAGGCGTGAGCCA[C/T]CGCGCCCGGCCCTGC | 54542 |
rs111772719 | snp | C/T | 0.5 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122891848 | GATGTGCTAAGTATG[C/T]AGTGATAAAATTTCA | 54542 |
rs111796343 | snp | G/T | 0.5 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122875995 | TAAGGGAAATAATGG[G/T]AGAAGGGGTGGACAG | 54542 |
rs111889837 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RC3H2 | GRCh38.p7 | 9:122850785 | GAGAAACCATTAATC[C/T]AGGTTGTCATTCTCC | 54542 |
rs111957293 | snp | C/T | 0.5 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122851865 | CCTCCACCTCCCAGC[C/T]GCCTGCCTTGGCCTC | 54542 |
rs111999735 | snp | A/C | 0.5 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122876735 | TAAAAAACAAAACAA[A/C]AAAAATTGGATAATA | 54542 |
rs111999853 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | RC3H2 | GRCh38.p7 | 9:122894508 | GGGGACTGGAAATAC[C/T]AGCGAGGGGTTACAA | 54542 |
rs112002260 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | RC3H2 | GRCh38.p7 | 9:122854949 | ATACAAAATACTCTC[C/T]ACTAAAAATACAAAA | 54542 |
rs112010654 | in-del | -/TTTT | 0.5 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122887742 | TTTTATACTTGTATC[-/TTTT]TTTTTTTTTTTTTTT | 54542 |
rs112135467 | snp | A/G | | | upstream-variant-2KB | RC3H2 | GRCh38.p7 | 9:122906385 | AAAATACAAAAATTA[A/G]CCGGGTGTGGTGGCG | 54542 |
rs112158274 | snp | C/T | 0.5 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122861797 | GATTAGTCTAGCAGA[C/T]GTTTACTTCTATGTG | 54542 |
rs112170921 | snp | A/C | 0.232651 | 0.249397 | intron-variant | RC3H2 | GRCh38.p7 | 9:122866556 | ATTGCAGGCGCGCGC[A/C]GCCACGCCTGACTGG | 54542 |
rs112227631 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | RC3H2 | GRCh38.p7 | 9:122866484 | GTACTGCTGCCATCT[C/T]GGCTCACTGCAACCT | 54542 |
rs112254934 | snp | C/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122868111 | CCACCCCGTCCAGGA[C/G]GGAGGTGGGGGTGTC | 54542 |
rs112284940 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | RC3H2 | GRCh38.p7 | 9:122907084 | TTTTTTTTTTGAGAC[A/G]GAGTCTCACTCTGTC | 54542 |
rs112522167 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RC3H2 | GRCh38.p7 | 9:122864613 | GAGAGTGTGGCTCCA[A/G]AGAGTCCCCTCCTTT | 54542 |
rs112527317 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RC3H2 | GRCh38.p7 | 9:122882684 | TGGGGTTCTTCTCTA[C/T]CCTTTCCACTAAACA | 54542 |
rs112528147 | snp | C/T | 0.5 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122892014 | ATGCATACATGAAGC[C/T]GTCTTAATAGGACTT | 54542 |
rs112557614 | snp | A/G | 0.0329836 | 0.124112 | intron-variant, upstream-variant-2KB | RC3H2, SNORD90 | GRCh38.p7 | 9:122882038 | AGGCTGCAGTGAACT[A/G]TGATGGCACCACTGC | 54542 |
rs112657504 | snp | G/T | 0.5 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122851312 | CTCAATTATCTAATT[G/T]TGGCACTTACTTCAA | 54542 |
rs112743935 | snp | A/G | 0.5 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122898516 | GCACTTTGAGAGGCC[A/G]AGGTGGGAGGATCAC | 54542 |
rs112747334 | snp | A/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122903116 | TAGAATATTTAAATT[A/T]TAAAGTAATACTTAG | 54542 |
rs112778103 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | RC3H2 | GRCh38.p7 | 9:122852619 | GCCAGCCGCCCTGAC[C/T]GGGAGGGAGGTGGAG | 54542 |
rs112819739 | snp | C/T | 0.5 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122865951 | TGTATTCAAAAAAAC[C/T]TTTTGAGGGAGTGGA | 54542 |
rs112900113 | snp | C/G | 0.5 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122866302 | ATTGGATATAATACT[C/G]TAATACACAAAAGGA | 54542 |
rs112912533 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | RC3H2, SNORD90 | GRCh38.p7 | 9:122881072 | AGTTATAAGGCTTGA[C/T]GGCAACAAAGAGGAA | 54542 |
rs113096348 | snp | C/T | 0.5 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122896646 | AACATACTATATACC[C/T]ATTACTGAATAAAGT | 54542 |
rs113100687 | snp | C/T | 0.5 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122899460 | TTACAGGGCTTGCTA[C/T]GTAAAAAGCACCCCT | 54542 |
rs113130808 | snp | C/G | 0 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122873476 | CTAGCACTTTGGGAG[C/G]CTGAGGTGGGCAGAT | 54542 |
rs113136408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122901685 | CAACCTCCGCCTCCC[A/G]GTTTCATACGATTCT | 54542 |
rs113172495 | snp | C/T | | | upstream-variant-2KB | RC3H2 | GRCh38.p7 | 9:122907201 | CAGTAGCTGGAATTA[C/T]AGGCACCCGTCATCA | 54542 |
rs113200613 | snp | C/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122867831 | CCCTCCGCCCGGCAG[C/T]CGGCCCATCTGAGAA | 54542 |
rs113252761 | in-del | -/T | 0.5 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122895984 | CTATAGCACATGTTC[-/T]TTTTTTTTTTCCCCC | 54542 |
rs113515510 | snp | C/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122869000 | TCCGCCTCCTGGGTT[C/T]AAGTGATTCTTCTGC | 54542 |
rs113518112 | snp | A/C | 0.5 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122862439 | TCTCCATCCACAAGG[A/C]CCTTCCTTCCTTGCT | 54542 |
rs113654361 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | RC3H2 | GRCh38.p7 | 9:122874594 | ATAATCTCAGTTCAC[A/G]GCAGACCTGACCTCC | 54542 |
rs113662372 | snp | A/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122870166 | GATTACCTGAGGTCA[A/G]GAGTTCAAGACCAGC | 54542 |
rs113837436 | snp | A/C | 0.5 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122901532 | TTACTTCTTAAATAC[A/C]CTATGTGGTTGAACT | 54542 |
rs113911016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122863961 | AGGCTGGTCTTGAAC[A/G]CCCAACCTCAGGTGA | 54542 |
rs113970852 | snp | A/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122897015 | TGGGTGACAGAGTGA[A/G]ACTCTGTCTAAAAAA | 54542 |
rs114145607 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | RC3H2, SNORD90 | GRCh38.p7 | 9:122881867 | ACATGATCAGATTTA[C/T]GCTTTAAAAAACATC | 54542 |
rs114166000 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | RC3H2 | GRCh38.p7 | 9:122898165 | AAGACTGTGATGACT[A/G]AGAGATGATTAAGAG | 54542 |
rs114333149 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | RC3H2 | GRCh38.p7 | 9:122883150 | GTAACATGAATTTCA[C/G]GAAGTCTCTGTCTCA | 54542 |
rs114406313 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | RC3H2 | GRCh38.p7 | 9:122869715 | ACATTATAGGCGCGC[G/T]CCTGCCAACACACCT | 54542 |
rs114505207 | snp | A/G | 0.00134218 | 0.0258706 | intron-variant | RC3H2 | GRCh38.p7 | 9:122854102 | CTATATGAGGAGGGA[A/G]AAAAAGAAAAGTTAG | 54542 |
rs114586646 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | RC3H2 | GRCh38.p7 | 9:122870056 | CCTATACAGAATATC[A/G]TGTCTCCTTGCTTTC | 54542 |
rs114591637 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RC3H2 | GRCh38.p7 | 9:122900123 | CCTTAGTATAGTTTT[A/G]TGTTACAATAGTCCT | 54542 |
rs114671094 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | RC3H2 | GRCh38.p7 | 9:122876749 | ACAAAAATTGGATAA[C/T]AGTATTAAACCTTAC | 54542 |
rs114677534 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | RC3H2 | GRCh38.p7 | 9:122890796 | TTGTATATAAGACAT[C/T]TAGAATACTGCTTAA | 54542 |
rs114750530 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RC3H2 | GRCh38.p7 | 9:122891532 | CTTGCTAAATTGGTT[A/G]AATTAGTTAATTCTT | 54542 |
rs114811627 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | RC3H2 | GRCh38.p7 | 9:122888169 | AGACCAGAATTATGA[A/G]CAATATGACAAACAA | 54542 |
rs114915708 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | RC3H2 | GRCh38.p7 | 9:122904536 | GGGAAAGAAGAAAGC[C/G]ATAGCAGAATTTCCT | 54542 |
rs115080158 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | RC3H2 | GRCh38.p7 | 9:122869503 | TGCTCCTAGATTAGA[C/G]TGGCTAAAAGTGAAG | 54542 |
rs115129036 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | RC3H2 | GRCh38.p7 | 9:122871627 | TGCGCCTGGCCAAAT[A/G]TTGTATCTTCTAAGA | 54542 |
rs115139512 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | RC3H2 | GRCh38.p7 | 9:122861844 | TGTAAAAAATAACTA[A/C]GGAACTGTGGGTAAT | 54542 |
rs115226112 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RC3H2 | GRCh38.p7 | 9:122891267 | ACCCCAAATGATCTG[C/T]CCGCCTCGGCCTCTC | 54542 |
rs115266315 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RC3H2 | GRCh38.p7 | 9:122863673 | AGTGCATAAATAACA[C/T]TTGTTAACTAGACCA | 54542 |
rs115440962 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | RC3H2 | GRCh38.p7 | 9:122869598 | AGGCGGAGTTTTGCT[C/T]GTCACCCAGGCTGGA | 54542 |
rs115450350 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | RC3H2 | GRCh38.p7 | 9:122876022 | ACAGCGAGAGATTTA[A/G]GACTAGTGAGAAGGC | 54542 |
rs115509262 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RC3H2 | GRCh38.p7 | 9:122863525 | ATTTCTCCCAGCAAT[A/G]TAAAATTTTCCTGTC | 54542 |
rs115873473 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RC3H2 | GRCh38.p7 | 9:122873105 | GGGGTGTATAATAGA[A/G]AAAGAAAATATAGGT | 54542 |
rs115882382 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RC3H2 | GRCh38.p7 | 9:122884835 | TCCAGCCTGGCGACA[C/T]AGCGAAAGTCCGTCT | 54542 |
rs115882478 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | RC3H2 | GRCh38.p7 | 9:122892373 | CCACCTTAGCCTTAT[A/G]AAGTGCTCAGATTAC | 54542 |
rs116119368 | snp | G/T | 0.445328 | 0.156035 | intron-variant | RC3H2 | GRCh38.p7 | 9:122868922 | TTTTTTTGTGGGGGG[G/T]TTAAGTTCCACTCTT | 54542 |
rs116157662 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | RC3H2, SNORD90 | GRCh38.p7 | 9:122880945 | AATGTCCTGACCACA[A/G]ATTCTTTCTGGAACA | 54542 |
rs116279498 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RC3H2 | GRCh38.p7 | 9:122861734 | ACAATCATTTTAAAG[A/G]TAGGATATAAAGAAA | 54542 |
rs116363230 | snp | C/T | 0.00286879 | 0.0377646 | intron-variant, upstream-variant-2KB | RC3H2, SNORD90 | GRCh38.p7 | 9:122880321 | CACTTAGAAAACTTA[C/T]AAGCTGTATTAACTC | 54542 |
rs116796340 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | RC3H2 | GRCh38.p7 | 9:122856540 | GATTATAGGCATGAG[A/C]CACTACACCAAGCTG | 54542 |
rs116901296 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | RC3H2 | GRCh38.p7 | 9:122863113 | CTAAACCCCTAGAAA[C/T]CATTAATCTACTTCC | 54542 |
rs116954343 | snp | A/C | 0.0644693 | 0.167566 | intron-variant | RC3H2 | GRCh38.p7 | 9:122896770 | GCTCACACCTGTAGT[A/C]CTAGCACCCTGGGAG | 54542 |
rs117025569 | snp | C/T | 0.0372196 | 0.131242 | upstream-variant-2KB | RC3H2 | GRCh38.p7 | 9:122906303 | TTTGGGAGGCCGAAG[C/T]GGGTGGACCGCCAGG | 54542 |
rs117069586 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | RC3H2 | GRCh38.p7 | 9:122892395 | TCAGATTACAGGCAT[A/G]AAGCCACCACACCCA | 54542 |
rs117136260 | snp | C/T | 0.0603597 | 0.1629 | intron-variant | RC3H2 | GRCh38.p7 | 9:122886228 | TCCACATGCAGCATG[C/T]ATCAGTATTTATTCC | 54542 |
rs117281773 | snp | C/T | 0.000298626 | 0.0122157 | intron-variant | RC3H2 | GRCh38.p7 | 9:122892873 | AATGTACTACCAAGT[C/T]CTACTTATCAGTAAA | 54542 |
rs117294809 | snp | A/C | 0.0158176 | 0.0875135 | synonymous-codon | RC3H2 | GRCh38.p7 | 9:122865360 | CTACTTTTCAGTTAC[A/C]GAATCTGCAGAGGGC | 54542 |
rs117338393 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | RC3H2 | GRCh38.p7 | 9:122903413 | TTCAACTTTTGAATA[C/T]AAAATCCTGAGTGTA | 54542 |
rs117385878 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | RC3H2 | GRCh38.p7 | 9:122857563 | GGAAAATACCTGCCC[C/T]CTAAGGTTTTTGTGA | 54542 |
rs117457560 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | RC3H2 | GRCh38.p7 | 9:122877098 | TGTTGTGAGGCAGAG[C/T]CTTGCTGTGTCCCTC | 54542 |
rs117650396 | snp | A/G | 0.10237 | 0.201756 | intron-variant | RC3H2 | GRCh38.p7 | 9:122898706 | GTGAGCCGAGATCAC[A/G]TCATCGCACTCCAGC | 54542 |
rs117678776 | snp | A/G | 0.0482946 | 0.147699 | intron-variant | RC3H2 | GRCh38.p7 | 9:122879440 | AATTTACATATAGAA[A/G]TTCAATACAGAAAAA | 54542 |
rs117835102 | snp | A/G | 0.0644693 | 0.167566 | intron-variant | RC3H2 | GRCh38.p7 | 9:122900342 | AAACTTCCCTTATAC[A/G]ATCAGATGTAAGAAA | 54542 |
rs117887020 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RC3H2 | GRCh38.p7 | 9:122857182 | TTATTCTCTCTATAC[C/T]TGTATATGTTTGAAA | 54542 |
rs118011517 | snp | C/T | 0.0648419 | 0.167978 | intron-variant | RC3H2 | GRCh38.p7 | 9:122869712 | TGCACATTATAGGCG[C/T]GCGCCTGCCAACACA | 54542 |
rs137888840 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RC3H2 | GRCh38.p7 | 9:122885132 | AAAAATTTAATGAAT[A/G]TAATATTGTTACATA | 54542 |
rs138023866 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RC3H2 | GRCh38.p7 | 9:122891454 | GTTCACTACTTCCAA[C/T]TCCTTGTTTCACAAT | 54542 |
rs138104483 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RC3H2 | GRCh38.p7 | 9:122860316 | ATTCACGTGATCATC[A/G]TAACAGATGTCATAT | 54542 |
rs138160146 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | RC3H2 | GRCh38.p7 | 9:122870044 | TTCCTCAGAGTTCCT[A/C]TACAGAATATCGTGT | 54542 |
rs138162342 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RC3H2 | GRCh38.p7 | 9:122856556 | CACTACACCAAGCTG[A/G]GTTTATAATTTTCTT | 54542 |
rs138283522 | snp | C/T | 0.000465279 | 0.0152454 | intron-variant | RC3H2 | GRCh38.p7 | 9:122875285 | TCACAATGCTGCTGC[C/T]TGTAGAGCTCATTAT | 54542 |
rs138309076 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RC3H2 | GRCh38.p7 | 9:122899604 | ATTAATGCCATCAAT[C/G]TAAAAACCAATTAGT | 54542 |
rs138424731 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RC3H2 | GRCh38.p7 | 9:122906213 | ACCCCTTGTTACTGA[G/T]GAGAAACTAAAGAAT | 54542 |
rs138626010 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | RC3H2 | GRCh38.p7 | 9:122891073 | CGCCCAGGCTGGAGT[A/G]CAGTGGCACAATCTC | 54542 |
rs138686675 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | RC3H2 | GRCh38.p7 | 9:122885888 | TTTTGTTTTGTTTTG[A/T]TTGTTTTGTTTTGTT | 54542 |
rs138757867 | snp | A/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122868356 | CCGTGTCTGTGTGGA[A/T]AGAAGTAGACATGGG | 54542 |
rs138810699 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RC3H2 | GRCh38.p7 | 9:122898877 | ACTTAACATAAGTCT[C/G]ACAAAAGCTCTCTGG | 54542 |
rs138832089 | in-del | -/GTT | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122875480 | CATTGTCTGTGGCTG[-/GTT]TTTTTTTGCTACAGT | 54542 |
rs138840332 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RC3H2 | GRCh38.p7 | 9:122870524 | AAATAAAATCTTAAC[C/G]AAGTGAGGTAAAGCA | 54542 |
rs138847210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122900490 | TCAAAACAGGCACTT[C/T]GTAAACATTTACCTA | 54542 |
rs138970845 | snp | C/T | 0.000630454 | 0.0177434 | missense | RC3H2 | GRCh38.p7 | 9:122865631 | GTTCTTACAGTGGCA[C/T]TGATCTTTTTGTTCC | 54542 |
rs138976276 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RC3H2 | GRCh38.p7 | 9:122895901 | AATGCAAAGTAGACC[C/G]TCATTAAATATGTTA | 54542 |
rs139151342 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RC3H2 | GRCh38.p7 | 9:122877011 | TCCAGCTATAAAATG[A/G]TCTCAAAATATGACC | 54542 |
rs139344486 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant, downstream-variant-500B | RC3H2 | GRCh38.p7 | 9:122853640 | GCCTGTAATCCCAGC[C/T]ACTCGGGAAGCTGAG | 54542 |
rs139399393 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RC3H2 | GRCh38.p7 | 9:122876259 | GTACAATGGAAGGCA[A/G]GAGGAGGAGGTATGG | 54542 |
rs139467309 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RC3H2 | GRCh38.p7 | 9:122872058 | ATTGGAATTACAGGC[A/G]TGAGCCACCTCACCC | 54542 |
rs139505008 | in-del | -/A/AA | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122897050 | AAAAAAAAAAAAAAA[-/A/AA]GGCCACATAAGATAC | 54542 |
rs139664866 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RC3H2 | GRCh38.p7 | 9:122901301 | CCCCGTTTAGAAAAC[A/T]TAAAAATAATTAGTT | 54542 |
rs139678472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122887043 | TCACTTTTAGTAATG[C/T]TAAGATTTATCAGTG | 54542 |
rs139681573 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RC3H2 | GRCh38.p7 | 9:122857679 | CTATTAATAAAACAA[C/G]CATAAAATAATTATA | 54542 |
rs139708769 | in-del | -/C | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122901586 | AACTTCCAATGCATT[-/C]TTTTTTTTTTTTTTT | 54542 |
rs139778020 | snp | A/C | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122897582 | GTTTTGTAAGCTAGA[A/C]ATGGACAAAAGTATG | 54542 |
rs139822134 | in-del | -/TCTCGAAC | 0.268724 | 0.249298 | intron-variant | RC3H2 | GRCh38.p7 | 9:122895384 | TGTTGTCCAGGCTAG[-/TCTCGAAC]TCCTGGCCTCAAGCA | 54542 |
rs139846650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122896488 | ATATACATAAATTTT[A/G]GCCACAGAATTGAAT | 54542 |
rs139851436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122893959 | TGTATTTTGTAGTGC[C/T]GCTATAAAAGTTCAA | 54542 |
rs139906063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RC3H2, SNORD90 | GRCh38.p7 | 9:122882105 | TTAAAAAAAAAATGA[A/G]AAGAAGAAATGTTCT | 54542 |
rs139992954 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | RC3H2 | GRCh38.p7 | 9:122877307 | CTGAGCACAAGCAAT[C/T]CTCCTGCCTCAGCCC | 54542 |
rs140020630 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RC3H2 | GRCh38.p7 | 9:122892653 | TCTGATCTTGTGATC[C/T]GCCCGCGCTGGCCTC | 54542 |
rs140117081 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | RC3H2 | GRCh38.p7 | 9:122861735 | CAATCATTTTAAAGG[C/G/T]AGGATATAAAGAAAA | 54542 |
rs140203538 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RC3H2 | GRCh38.p7 | 9:122858410 | TTTCCTATCCAAATA[C/T]AACATTTATTGAGCA | 54542 |
rs140216725 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RC3H2 | GRCh38.p7 | 9:122897944 | TTTTTTGTTTTGTTG[C/T]TTAAAAAAGTGTTTC | 54542 |
rs140237501 | snp | A/G | 5.09178e-05 | 0.00504542 | intron-variant | RC3H2 | GRCh38.p7 | 9:122854502 | AAGTCTGAGAATGGA[A/G]AATCATATAGAATTA | 54542 |
rs140276728 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RC3H2 | GRCh38.p7 | 9:122876520 | GTGGTTCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 54542 |
rs140412536 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RC3H2 | GRCh38.p7 | 9:122869373 | ATGCCTTCACAATAG[C/T]TTCCCTTTTAGTCCT | 54542 |
rs140445530 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RC3H2 | GRCh38.p7 | 9:122872940 | CCCCAGAATGTAGCA[A/G]TTCTTTGGAACATAA | 54542 |
rs140516825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122874974 | AATTGAGGGTGGAAT[A/G]GCAATGAAACCACAG | 54542 |
rs140674103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122859182 | TAAATCTAAGGCAGC[C/T]CTTAATGTAGGAAAA | 54542 |
rs140715639 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RC3H2 | GRCh38.p7 | 9:122894391 | TTTTGCCTTTGTGGA[A/G]CTCACATTCTAGTGG | 54542 |
rs140725070 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122892348 | AAACTCCTGGGCTCA[A/T]GAAATCTACCCACCT | 54542 |
rs140763976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122890787 | ATTTTTTAATTGTAT[A/G]TAAGACATTTAGAAT | 54542 |
rs140988604 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RC3H2 | GRCh38.p7 | 9:122878909 | ATCCACCACAATGCC[C/T]GGCTCATTTTTGTAT | 54542 |
rs141095156 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | RC3H2 | GRCh38.p7 | 9:122884637 | GTGGGCACATCACCT[A/G]AGGTCATGAGTTCGA | 54542 |
rs141179931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122870114 | GCATGGTGGCTCACA[C/T]CTGTAATCCCAGCAC | 54542 |
rs141216989 | snp | A/G | 0.0648419 | 0.167978 | intron-variant | RC3H2 | GRCh38.p7 | 9:122876555 | ATCGTTTGAACAGGG[A/G]AGGCAGAGGTTGCAG | 54542 |
rs141218584 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RC3H2 | GRCh38.p7 | 9:122874248 | AAGTATACAAATGGC[A/G]GAGTAGAGCTAGAGG | 54542 |
rs141237981 | snp | C/G | 0.000513402 | 0.0160137 | missense | RC3H2 | GRCh38.p7 | 9:122855389 | CTTAACATCACCACT[C/G]TCCAGGTCCTATGTA | 54542 |
rs141269371 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | RC3H2 | GRCh38.p7 | 9:122862651 | TGTAATCCCAGCCTT[C/T]TGGGAGGCCAAGGCG | 54542 |
rs141295900 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RC3H2 | GRCh38.p7 | 9:122902774 | TGAGAATTGCTTGAA[C/T]CTGGAAGCAGAGGTT | 54542 |
rs141480404 | snp | A/T | 0.0193772 | 0.0965046 | upstream-variant-2KB | RC3H2 | GRCh38.p7 | 9:122905512 | CACCCCGATCACGTG[A/T]CAAGGGAGCCCCGGA | 54542 |
rs141626332 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RC3H2 | GRCh38.p7 | 9:122891396 | TATTTCCTAGTCTAG[C/T]GCCTTAACTACTTAG | 54542 |
rs141668736 | in-del | -/AAACAAAC | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122870378 | AGACTCTGTCTCCAA[-/AAACAAAC]AAACAAACAAACAAA | 54542 |
rs141695567 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RC3H2 | GRCh38.p7 | 9:122886183 | GTGTGAGCCACCGTG[C/T]CCAACCTAACGTAGT | 54542 |
rs141751838 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RC3H2 | GRCh38.p7 | 9:122888032 | TTACAGGCGTGAGCC[A/G]CTGCGCCTGGCCTTG | 54542 |
rs141890005 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, downstream-variant-500B | RC3H2, SNORD90 | GRCh38.p7 | 9:122879842 | AGCTACCATTGCATT[C/T]TCCAGCTGCTCCCAA | 54542 |
rs142022595 | snp | G/T | 0.030278 | 0.119257 | intron-variant | RC3H2 | GRCh38.p7 | 9:122871512 | CCGTGTTAGTGGGGG[G/T]GGGGGTTTCATCGTG | 54542 |
rs142035894 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | RC3H2 | GRCh38.p7 | 9:122862338 | CCTAGTGAGCATGAG[A/G]TCACTATCCTAGATG | 54542 |
rs142037109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122871126 | ACCTTCCTGCACCTG[C/T]AGCCACATTCCTCTT | 54542 |
rs142099395 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RC3H2 | GRCh38.p7 | 9:122865792 | TCTTCAGCTAAATAA[C/T]CAAATACAGTCTATA | 54542 |
rs142172072 | snp | A/G | 0.0648419 | 0.167978 | intron-variant | RC3H2 | GRCh38.p7 | 9:122868945 | CCACTCTTGTCGCCC[A/G]GGTTACAGTGCAATG | 54542 |
rs142192853 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | RC3H2 | GRCh38.p7 | 9:122869045 | TAGCTGGGATTACAG[G/T]CACGTGCCTGCCACC | 54542 |
rs142330394 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant, downstream-variant-500B | RC3H2 | GRCh38.p7 | 9:122853427 | TTATACCTGTGGAAC[C/T]TGGGGTTTCCCTTTT | 54542 |
rs142378888 | snp | C/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122896934 | GGGAGGCTGAAGCAG[C/G]AGAATCGCTTGAACC | 54542 |
rs142442777 | in-del | -/A | 0.00953873 | 0.0683987 | intron-variant | RC3H2 | GRCh38.p7 | 9:122885035 | TTGAATAAATACTAT[-/A]AAAGATATTTTTGGA | 54542 |
rs142485625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122885310 | TGTCGGTAAAGAATA[C/T]ATAAAAAATTCTCTG | 54542 |
rs142537235 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | RC3H2 | GRCh38.p7 | 9:122902023 | CAACCTCCGTCTCCC[A/G]GGTTCAAGCGATTCT | 54542 |
rs142676767 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RC3H2 | GRCh38.p7 | 9:122886644 | ACAGTGGGCTATAAG[C/T]GTGCCACTGCACTCC | 54542 |
rs142704765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122873993 | CAGCTAACTATACCA[C/T]AATTTTTAAACTACT | 54542 |
rs142845696 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RC3H2 | GRCh38.p7 | 9:122861530 | GAAAAAAAACCATAT[A/G]TATATGGCCAAAGCT | 54542 |
rs142879820 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | RC3H2 | GRCh38.p7 | 9:122896061 | TTCCGTGGGCCATAC[C/T]GGAAGAATTGTCTTG | 54542 |
rs142884919 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RC3H2 | GRCh38.p7 | 9:122865230 | GTGTTTCTTCTACAT[C/T]ACAAAATATTCTGCA | 54542 |
rs142910146 | snp | C/T | 0.0670745 | 0.170406 | upstream-variant-2KB | RC3H2 | GRCh38.p7 | 9:122906298 | AGCACTTTGGGAGGC[C/T]GAAGCGGGTGGACCG | 54542 |
rs142946884 | snp | C/T | 0.021333 | 0.101051 | intron-variant | RC3H2 | GRCh38.p7 | 9:122892480 | GCAGTGGCACCATCT[C/T]GGCTCACTGCAAGCT | 54542 |
rs143151577 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122898873 | CAAGACTTAACATAA[C/G]TCTGACAAAAGCTCT | 54542 |
rs143310362 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RC3H2 | GRCh38.p7 | 9:122876336 | TATGCCCACAAAGAG[C/T]TGATAGACAGGGCAG | 54542 |
rs143370507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122872073 | GTGAGCCACCTCACC[C/T]GGCCCCCAATTATTA | 54542 |
rs143382177 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | RC3H2 | GRCh38.p7 | 9:122889528 | AGTTCAAACAATAAA[C/T]CTTCAAGAAGAAAAC | 54542 |
rs143395142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122876048 | AAGGCAACAAGGGAT[C/T]GAGAAAAGGAGATGA | 54542 |
rs143466192 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | RC3H2 | GRCh38.p7 | 9:122878037 | TGTCAGCTTGAGGGT[C/G]CAACTCTCAGGCTTA | 54542 |
rs143484414 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | RC3H2 | GRCh38.p7 | 9:122895326 | TCACACACCACCATG[C/T]CTGACTAATTTTTTT | 54542 |
rs143507099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122882445 | CTCTTGGGGGCTATA[A/G]AACCAACAAAATAAC | 54542 |
rs143679673 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | RC3H2 | GRCh38.p7 | 9:122864816 | TTTTTAGTAGAGATG[C/G]GGTTTCACCATGTCA | 54542 |
rs143715355 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RC3H2 | GRCh38.p7 | 9:122878562 | GACATGAGCCACCGC[A/G]CCCAGCCCCCTGACA | 54542 |
rs143726986 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | RC3H2 | GRCh38.p7 | 9:122857590 | GTGAGAATTAAATAA[A/G]ATAGCTTTATGCAAA | 54542 |
rs143761340 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | RC3H2 | GRCh38.p7 | 9:122860395 | ATTCATTAGTCACCA[C/T]TTACCCATTCTTTTT | 54542 |
rs143786243 | snp | A/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122871321 | TTTTTTTTTTGAGAC[A/G]GAGTCTCGCTCTGTT | 54542 |
rs143886635 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | RC3H2 | GRCh38.p7 | 9:122858573 | CTTCCTTAAGTCACA[A/C]AATTAGTAAGTGGAG | 54542 |
rs143942926 | snp | A/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122868363 | TGTGTGGAAAGAAGT[A/G]GACATGGGAGACTTT | 54542 |
rs144355425 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RC3H2 | GRCh38.p7 | 9:122858273 | ATTTATTCAACTGAT[A/G]TTAAACGCAGAATCT | 54542 |
rs144484957 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RC3H2 | GRCh38.p7 | 9:122897879 | ACAAGCAAATTAACT[A/T]TCCATATTCCATTTT | 54542 |
rs144495757 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RC3H2, SNORD90 | GRCh38.p7 | 9:122881223 | CAGGGATGGTGGCTC[A/C]TGCCTGTAATCCCAG | 54542 |
rs144526212 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | RC3H2 | GRCh38.p7 | 9:122901546 | CACTATGTGGTTGAA[C/G]TGTTTTAAAATAAAT | 54542 |
rs144682619 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RC3H2 | GRCh38.p7 | 9:122890931 | TCCATCATTACAGAA[A/T]AAGAACAAGTATGCT | 54542 |
rs144700265 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | RC3H2 | GRCh38.p7 | 9:122883548 | TAAAAAGTAATCAAG[C/G]AAAATAAAACATACT | 54542 |
rs144714368 | snp | C/T | 0.000828377 | 0.0203348 | missense | RC3H2 | GRCh38.p7 | 9:122858072 | GCTCCTCGCAACTGG[C/T]CTTCAAATGACCACA | 54542 |
rs144924341 | snp | C/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122898475 | AATGTTCCTGCTGGG[C/T]GTGGTGGCTCACACC | 54542 |
rs145057859 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RC3H2 | GRCh38.p7 | 9:122870366 | GCCGACAGAGCAAGA[C/T]TCTGTCTCCAAAAAC | 54542 |
rs145187712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122883141 | CTAGACTGGGTAACA[C/T]GAATTTCAGGAAGTC | 54542 |
rs145296333 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RC3H2 | GRCh38.p7 | 9:122854871 | CACTTTGCGAGGCTG[A/G]GGCGGGTGGATCACA | 54542 |
rs145430378 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RC3H2 | GRCh38.p7 | 9:122892706 | GTGAGCCACCGCGCC[C/T]GGCTCTAGCTTGAAT | 54542 |
rs145580670 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RC3H2 | GRCh38.p7 | 9:122873628 | TGAGGTGGGAGAATC[C/T]CCTGAGCCTGGGAGG | 54542 |
rs145601849 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RC3H2 | GRCh38.p7 | 9:122888117 | TTTGCTTGCTTGTTT[G/T]ATCCAACTGTGTGTC | 54542 |
rs145960809 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122885810 | CACTGTTCATACACT[C/G]TATACACAGCCCCTG | 54542 |
rs146009992 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | RC3H2, SNORD90 | GRCh38.p7 | 9:122881826 | CACTGCACAGAGCTG[A/C]TTGAGGATTTTTAAG | 54542 |
rs146082777 | snp | C/T | 8.28617e-05 | 0.00643615 | synonymous-codon | RC3H2 | GRCh38.p7 | 9:122865615 | ATTTAGAAGAGGAAA[C/T]GTTCTTACAGTGGCA | 54542 |
rs146123046 | snp | C/T | | | upstream-variant-2KB | RC3H2 | GRCh38.p7 | 9:122906312 | CCGAAGCGGGTGGAC[C/T]GCCAGGTCAGAAGTT | 54542 |
rs146134455 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RC3H2 | GRCh38.p7 | 9:122861567 | GCTGGATTTGTAGCT[A/G]TATTTATTTTGCTGA | 54542 |
rs146141672 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RC3H2 | GRCh38.p7 | 9:122901684 | GCAACCTCCGCCTCC[C/T]GGTTTCATACGATTC | 54542 |
rs146179510 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RC3H2 | GRCh38.p7 | 9:122864444 | TTGTTCAAGGCATAC[C/T]GGAGTATTAATTCAC | 54542 |
rs146242167 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | RC3H2 | GRCh38.p7 | 9:122886416 | ATTCTTTTGGGTATA[C/T]ACCTAGGAATAAAAC | 54542 |
rs146262060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122882568 | CCAGCCAGCAACCTA[C/T]ACTCTTGGATCATAA | 54542 |
rs146322527 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB | RC3H2 | GRCh38.p7 | 9:122906182 | GCAAAGTGATCCTAG[A/G]AGACAGATACAATGT | 54542 |
rs146373449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122901097 | AGTTCAGGTCTACGG[C/T]ATCTGATTTTAAAAT | 54542 |
rs146420851 | snp | C/T | 0.030278 | 0.119257 | intron-variant | RC3H2 | GRCh38.p7 | 9:122854911 | GAGTTCCAGACCAGC[C/T]TGGCCAACATGGCGA | 54542 |
rs146430774 | snp | A/G | 0.00126028 | 0.025071 | synonymous-codon | RC3H2 | GRCh38.p7 | 9:122859068 | AACACAGGGAGCCAC[A/G]CCAGCTGGTACCGTT | 54542 |
rs146484373 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | RC3H2 | GRCh38.p7 | 9:122877153 | ACACTCACTGCAGCC[G/T]TGACCTATGGGGTTC | 54542 |
rs146503615 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RC3H2 | GRCh38.p7 | 9:122874212 | AATCAACAGTGATTA[A/G]TTGAATATACCTTAA | 54542 |
rs146607117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122858324 | TAGGGAAGTCATTTG[C/T]ATGTATGTGGTGATA | 54542 |
rs146624783 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122854411 | ATATTTTTCAGAAAT[G/T]TGTTATATAGCTCAG | 54542 |
rs146625117 | in-del | -/AACAAAC | 0.040671 | 0.13668 | intron-variant | RC3H2 | GRCh38.p7 | 9:122870407 | ACAAACAAACAAACA[-/AACAAAC]AAAAAAAAAACAACA | 54542 |
rs146784252 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RC3H2 | GRCh38.p7 | 9:122874866 | AAGTCTGGCAAAATA[C/T]AATAAAGTTCTGAAC | 54542 |
rs146795042 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RC3H2 | GRCh38.p7 | 9:122878179 | TTGTTTTTAATATTT[G/T]AAGTTATAATATCTT | 54542 |
rs146845098 | in-del | -/GTG | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122868914 | TTTTTTTTTTTTTTT[-/GTG]GGGGGGTTAAGTTCC | 54542 |
rs146851584 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | RC3H2 | GRCh38.p7 | 9:122879085 | AACTTCTAAAGTACA[C/T]TGAAAAGTATCTTGA | 54542 |
rs147002437 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RC3H2 | GRCh38.p7 | 9:122899061 | TCAATTATGCCAACA[C/T]ACAAAAAAATTCTAT | 54542 |
rs147012300 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122903763 | TCCAAATCAACGAAA[A/T]TGTCAATATTGAAAA | 54542 |
rs147012546 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | RC3H2 | GRCh38.p7 | 9:122856100 | TTAAGTGCTCATATG[A/G]AACATTTGACTAATA | 54542 |
rs147077877 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | RC3H2 | GRCh38.p7 | 9:122859234 | CCTTACCCTGCTTTA[C/T]AAAGCTTTATACCCT | 54542 |
rs147107729 | snp | C/T | 1.74072e-05 | 0.00295013 | intron-variant, nc-transcript-variant | RC3H2, SNORD90 | GRCh38.p7 | 9:122880270 | GATGAATTAAATTTT[C/T]ACCTCAGAATCTGCC | 54542 |
rs147115968 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | RC3H2 | GRCh38.p7 | 9:122884428 | TTTTGTATATAATTT[A/T]AAAAATGATATTAGC | 54542 |
rs147149948 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | RC3H2 | GRCh38.p7 | 9:122876380 | CGTCTGTAATCCCAG[C/T]ACTTTGGGAGGCCAA | 54542 |
rs147352483 | snp | G/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122868914 | TTTTTTTTTTTTTTT[G/T]TGGGGGGGTTAAGTT | 54542 |
rs147418910 | in-del | -/GATT | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122864894 | CTCCAAAAGTGCTGG[-/GATT]ACAGGTGTGAACCAC | 54542 |
rs147423140 | snp | C/T | 1.65781e-05 | 0.00287902 | intron-variant | RC3H2 | GRCh38.p7 | 9:122851040 | TTTCTCTTTATTATG[C/T]CCTATGCCCACTGTT | 54542 |
rs147455740 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | RC3H2 | GRCh38.p7 | 9:122892513 | GCCTCCCGGGTTCAC[A/G]CCATTCTCCTGCCTC | 54542 |
rs147465875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122896459 | AAAATATTTCTTATC[C/T]ACCAATATCACTTAT | 54542 |
rs147620997 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | RC3H2 | GRCh38.p7 | 9:122863876 | CCAGGTAGCTGGGAT[C/T]ACAGGCATGCGCCAC | 54542 |
rs147893307 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RC3H2 | GRCh38.p7 | 9:122887967 | CCAGGTTAGTCTTGA[A/C]CTCCTGACCTCAGGT | 54542 |
rs148019578 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | RC3H2, SNORD90 | GRCh38.p7 | 9:122881349 | AAAACTAGTCAGGCA[C/T]GGTGGTGGCAGGCGC | 54542 |
rs148083183 | snp | A/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122864846 | AGCCAGGATGGTCTC[A/G]ATCTCCAGACCTCAT | 54542 |
rs148135666 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | RC3H2 | GRCh38.p7 | 9:122871359 | CTGGAGTGCAGTGGC[A/G]CAATCTCAGCTCACT | 54542 |
rs148153618 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RC3H2 | GRCh38.p7 | 9:122884574 | GAAATATTCTGAGAC[C/T]GGGCACGCTGGCTCA | 54542 |
rs148303140 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RC3H2 | GRCh38.p7 | 9:122860574 | GCATGCCACCACACT[A/C]GGCTAATTTTTAGTT | 54542 |
rs148448704 | snp | A/G | 0.312348 | 0.242101 | intron-variant | RC3H2 | GRCh38.p7 | 9:122873943 | CCGCCTCAGCCTCCC[A/G]AGCAGCTGGGATTAC | 54542 |
rs148492795 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RC3H2 | GRCh38.p7 | 9:122886506 | CAGCACACCATTTTA[C/T]GTGCCCACATTCTCC | 54542 |
rs148562505 | snp | C/T | 9.95388e-05 | 0.00705404 | missense | RC3H2 | GRCh38.p7 | 9:122858086 | GTCTTCAAATGACCA[C/T]AAGGTTCCTAATGGG | 54542 |
rs148613536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122862233 | CAAGGCAACAAGATC[C/T]ATGATAAGGTCAACA | 54542 |
rs148772976 | snp | A/G | 0.0644693 | 0.167566 | intron-variant | RC3H2 | GRCh38.p7 | 9:122896924 | CCAGCTACTTGGGAG[A/G]CTGAAGCAGGAGAAT | 54542 |
rs148792755 | in-del | -/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122905080 | CCCGGGCTGGGGCCC[-/G]GAGCCGCATCGTGCC | 54542 |
rs148877311 | snp | G/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122859891 | CAATGTTTCTTTTTT[G/T]CTTAGAATTGTCTAA | 54542 |
rs148921429 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RC3H2 | GRCh38.p7 | 9:122878517 | CCTTGTGATCCGCCC[A/G]CCTCAGCCTCCCAAA | 54542 |
rs148946841 | snp | G/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122868344 | ATCGGATGGTTGCCG[G/T]GTCTGTGTGGAAAGA | 54542 |
rs149110955 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RC3H2 | GRCh38.p7 | 9:122904543 | AAGAAAGCCATAGCA[A/G]AATTTCCTGGCTGTG | 54542 |
rs149174661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122883521 | CAAAGAGGACATCAC[A/G]CGTACATAATTTAAA | 54542 |
rs149227031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122889183 | CTTTTTCATTTGCTT[A/G]TAATTTTTTTGTGAT | 54542 |
rs149233614 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | RC3H2, SNORD90 | GRCh38.p7 | 9:122881109 | TTAAATTAGGGAGAA[C/G]AAAGGGATTTCAGAA | 54542 |
rs149234948 | in-del | -/AA | 0.0569829 | 0.158885 | intron-variant | RC3H2 | GRCh38.p7 | 9:122896121 | AATAGCTGATGAGTT[-/AA]AAAAAAAAAAAAAAA | 54542 |
rs149330930 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RC3H2 | GRCh38.p7 | 9:122850891 | CAACAAAAAGCAAGT[C/T]TCAGGCTACCAAAAT | 54542 |
rs149383248 | snp | C/T | 0.000399281 | 0.0141238 | splice-donor-variant | RC3H2 | GRCh38.p7 | 9:122857922 | TTAAAACCTTTCTTA[C/T]ATCCGCACGAAAGTC | 54542 |
rs149426124 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RC3H2 | GRCh38.p7 | 9:122906881 | TTTCAACTGGACAGT[A/G]ATAGGTAATTTACAT | 54542 |
rs149686328 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RC3H2 | GRCh38.p7 | 9:122902340 | CAATGGATAACTTCA[A/T]CCTTCATATTACCAA | 54542 |
rs149689387 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | RC3H2 | GRCh38.p7 | 9:122873162 | ACATTTGCTGAATTT[A/C]TGGTGTTATGTGAAC | 54542 |
rs149908015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122898334 | TATAACCAAAAACTG[C/T]AAAGTCCAATGAGGA | 54542 |
rs149996105 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | RC3H2 | GRCh38.p7 | 9:122882808 | AGGTGTTAATCTAAT[A/C]ACTACAGAGAATGAG | 54542 |
rs150045144 | snp | G/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122868916 | TTTTTTTTTTTTTGT[G/T]GGGGGGTTAAGTTCC | 54542 |
rs150059221 | snp | A/C/G | 0.0134861 | 0.0810011 | intron-variant | RC3H2 | GRCh38.p7 | 9:122866267 | CTGATACTAAGTTTT[A/C/G]AGTTTTATTTATGGT | 54542 |
rs150065807 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant, downstream-variant-500B | RC3H2 | GRCh38.p7 | 9:122853708 | AGTGAGCCAAGATCG[C/T]GCCATTGCACTCCAG | 54542 |
rs150168509 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | RC3H2 | GRCh38.p7 | 9:122895567 | AACAAAAATATACTG[A/G]CAATTAAATTAAGAT | 54542 |
rs150307232 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | RC3H2 | GRCh38.p7 | 9:122884739 | GCATCTGTAGTCACA[A/G]CTACTCAGAAGGCTG | 54542 |
rs150359291 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122891407 | CTAGTGCCTTAACTA[C/G]TTAGCCAATTGTAGA | 54542 |
rs150371050 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RC3H2 | GRCh38.p7 | 9:122869929 | CAAGAAGGGCATGAG[C/T]AGACCTATATTTCAG | 54542 |
rs150423020 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RC3H2 | GRCh38.p7 | 9:122875042 | GCTCCCCTTTTAGCT[A/C]AAAAGCTCTATTTCA | 54542 |
rs150641639 | snp | C/T | 0.021333 | 0.101051 | intron-variant | RC3H2 | GRCh38.p7 | 9:122900212 | AATTTCTACCACAAA[C/T]TGAATTAATACCTTT | 54542 |
rs150684265 | snp | C/G | 0.0648419 | 0.167978 | intron-variant | RC3H2 | GRCh38.p7 | 9:122871545 | AGCCAGGATAGTCCC[C/G]ATCTCCTGACCTTGT | 54542 |
rs150735425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122876885 | CCGTAAAAAGGATAT[A/G]TATCTGCTTTACCAT | 54542 |
rs150904928 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RC3H2 | GRCh38.p7 | 9:122865889 | TTAATATAGCAAGCC[A/G]AGTTTATATGTATTT | 54542 |
rs150928117 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | RC3H2 | GRCh38.p7 | 9:122902053 | TCCTGCCTCAGCCTC[C/T]GGAGTAGCTGGGATT | 54542 |
rs151051024 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | RC3H2 | GRCh38.p7 | 9:122878632 | TGGAAACAGCAACTA[C/T]ATTGCAGGTGGCTGT | 54542 |
rs151097081 | snp | C/G | 1.65971e-05 | 0.00288067 | missense | RC3H2 | GRCh38.p7 | 9:122892989 | TAGTGTTTATTCTCA[C/G]CTAGATTACTTAACT | 54542 |
rs151193923 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RC3H2 | GRCh38.p7 | 9:122869055 | TACAGGCACGTGCCT[C/G]CCACCACGCCTGGTT | 54542 |
rs151307731 | snp | A/G | 0.00716266 | 0.059414 | intron-variant, downstream-variant-500B | RC3H2 | GRCh38.p7 | 9:122853523 | TTGGGAAGGTGAGGC[A/G]AGCAGATCACTTGAG | 54542 |
rs180753084 | snp | A/G | 0.000150508 | 0.0086736 | missense | RC3H2 | GRCh38.p7 | 9:122854255 | GATAAATCAGTAACA[A/G]TGAATCTGTCCCTTT | 54542 |
rs180756661 | snp | A/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122884903 | TGGTCTGTATTCTTC[A/G]GGAATATCAGTGTCA | 54542 |
rs180758038 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122898252 | AAAACAAAAAAATTG[G/T]CTTAAATATCTTGTA | 54542 |
rs180771635 | snp | A/C | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122862120 | CATAGACTTATCAAC[A/C]AAAAGGCAACAAGAT | 54542 |
rs180794567 | snp | A/C | 1.65625e-05 | 0.00287766 | missense | RC3H2 | GRCh38.p7 | 9:122877513 | AATGTACAATTTGTT[A/C]CTCGTGGACAACCCC | 54542 |
rs180828869 | snp | C/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122879293 | CAGTTACTTGGGAGG[C/T]TGAGGCAGGAGAATC | 54542 |
rs180979761 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RC3H2 | GRCh38.p7 | 9:122904566 | TGGCTGTGTTTCATG[C/G]CATTGCTCCTAGCCA | 54542 |
rs180980114 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122871987 | CTTGCTATGTTGCCC[A/T]GGCTGGTCACAAACT | 54542 |
rs181004128 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RC3H2 | GRCh38.p7 | 9:122857777 | CTAGCCGTAGTGCAT[G/T]TATATTCAGTGTTTA | 54542 |
rs181017906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122891415 | TTAACTACTTAGCCA[A/G]TTGTAGATCACTACA | 54542 |
rs181055023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RC3H2, SNORD90 | GRCh38.p7 | 9:122881609 | GGCCATTATATACTA[C/T]GGCAGGGAATTTGGA | 54542 |
rs181284586 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RC3H2 | GRCh38.p7 | 9:122870481 | AAATAAAGTTTTAAC[C/T]ATGAACCTCTCAAAA | 54542 |
rs181316350 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | RC3H2, SNORD90 | GRCh38.p7 | 9:122881822 | AAACCACTGCACAGA[A/G]CTGATTGAGGATTTT | 54542 |
rs181401641 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | RC3H2 | GRCh38.p7 | 9:122905794 | CCCATTACAAAAACA[A/G]GAAGAAAACATGTAT | 54542 |
rs181412688 | snp | C/G | 0.000209435 | 0.010231 | intron-variant | RC3H2 | GRCh38.p7 | 9:122858655 | GACTACATTATAGTA[C/G]CATCTTCACTTACCC | 54542 |
rs181521779 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RC3H2 | GRCh38.p7 | 9:122882640 | ACCCGCTAGACTATT[A/C]GACAATGAAACTACA | 54542 |
rs181532769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122859202 | ATGTAGGAAAATATA[A/G]TAAGCTTTGAACCTT | 54542 |
rs181549764 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RC3H2 | GRCh38.p7 | 9:122906585 | GTAATTAAACTCAAG[G/T]CACTTTCCAATGTGA | 54542 |
rs181728764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122885330 | AAAATTCTCTGCATT[A/G]TTCTTACAACTTTTC | 54542 |
rs181731647 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122863500 | TTGTTTTTTTTCTGT[A/T]ATTTCCCATATTTCT | 54542 |
rs181751491 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | RC3H2 | GRCh38.p7 | 9:122890969 | CATCCATCTAAAATA[A/C]AAATATTTTCATTGA | 54542 |
rs181883544 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | RC3H2 | GRCh38.p7 | 9:122876703 | TTTGGTGAGGTCTCA[A/C]AAATGAAAGTCTTAG | 54542 |
rs181888047 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, downstream-variant-500B | RC3H2 | GRCh38.p7 | 9:122853480 | TGATCAGCCAGGCAC[A/G]GGGGCTCACACCTGT | 54542 |
rs181908559 | snp | C/G | 0.000233205 | 0.0107957 | missense | RC3H2 | GRCh38.p7 | 9:122897290 | TTACCTGGGCTCCAA[C/G]TAACTGGAGAAGTGC | 54542 |
rs182118328 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RC3H2 | GRCh38.p7 | 9:122864386 | TAATGGTGATAATAA[G/T]AATAAAGCAAATATT | 54542 |
rs182152034 | snp | C/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122887390 | TTTCAACAAAATTGT[C/T]TCTCCCTCCTCTCTT | 54542 |
rs182157450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122886351 | GACTATTGTGAATAA[C/T]GCTGCAATAAACATT | 54542 |
rs182382837 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RC3H2 | GRCh38.p7 | 9:122888027 | TGGGATTACAGGCGT[A/G]AGCCACTGCGCCTGG | 54542 |
rs182425488 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | RC3H2 | GRCh38.p7 | 9:122863926 | ATTTTTAGTAGAGAC[A/G]GGGTTTCTCCATGTT | 54542 |
rs182498186 | snp | A/G | 0.000303137 | 0.0123076 | intron-variant, upstream-variant-2KB | RC3H2, SNORD90 | GRCh38.p7 | 9:122880320 | ACACTTAGAAAACTT[A/G]TAAGCTGTATTAACT | 54542 |
rs182581875 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RC3H2 | GRCh38.p7 | 9:122861093 | TTGAGGCAAAACACA[C/T]CAACCTTTTATTATT | 54542 |
rs182589397 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RC3H2 | GRCh38.p7 | 9:122892654 | CTGATCTTGTGATCC[A/G]CCCGCGCTGGCCTCC | 54542 |
rs182589623 | snp | C/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122873101 | TAGAGGGGTGTATAA[C/T]AGAGAAAGAAAATAT | 54542 |
rs182753754 | snp | C/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122860529 | AGCAATCCTCCCACC[C/T]CAGCCTCCCAAGCAG | 54542 |
rs182776949 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | RC3H2 | GRCh38.p7 | 9:122856240 | ACAGTCCATATCCTA[A/T]AGGAGTTTATAATTT | 54542 |
rs182812378 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RC3H2 | GRCh38.p7 | 9:122901514 | GTATATATGACTCAA[A/G]TTTTACTTCTTAAAT | 54542 |
rs183030683 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RC3H2 | GRCh38.p7 | 9:122882973 | CCAAATGATTTCCTT[A/C]TGTTCTTTCCGTTAC | 54542 |
rs183041958 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | RC3H2 | GRCh38.p7 | 9:122849335 | CTCAGTTACTGCACC[A/G]GATTGCTACAAACTC | 54542 |
rs183045275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122865091 | AAAAAAACAATTCTG[A/G]TCCAGTCTCTTTGGG | 54542 |
rs183099916 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RC3H2 | GRCh38.p7 | 9:122883961 | TCACATCACTGCACT[C/T]CAGCCTGGGTAACAG | 54542 |
rs183216406 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RC3H2 | GRCh38.p7 | 9:122894656 | AGGCCAAGGTGGGCA[A/G]ATCACTTGAGGTCAG | 54542 |
rs183223717 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122874298 | CTGTGATGTACTGAG[C/G]AACTAATTAAGAATT | 54542 |
rs183226524 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RC3H2 | GRCh38.p7 | 9:122850462 | GATAGATAGATAATT[G/T]TGAGATGGAGTCTCA | 54542 |
rs183366155 | snp | A/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122873736 | TAACCCATGAGATAA[A/G]TGAAGTCCAGTGAAA | 54542 |
rs183440635 | snp | C/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122879381 | CCTGGGTGACAGAGT[C/G]AGACTTTGTCTAAAA | 54542 |
rs183443405 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RC3H2 | GRCh38.p7 | 9:122900633 | CTAGACCTATACTAA[C/T]ACATTTTATGCAACT | 54542 |
rs183452944 | snp | A/T | 0.00759837 | 0.0611674 | intron-variant | RC3H2 | GRCh38.p7 | 9:122855890 | AGAACTGGTTAAAAA[A/T]AAATAAATAAAGCCA | 54542 |
rs183573656 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RC3H2 | GRCh38.p7 | 9:122850016 | GAGTCTCCCTCCGTC[A/G]CCCAGGCTGGAGTGC | 54542 |
rs183590561 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RC3H2 | GRCh38.p7 | 9:122894115 | ATACAAAAAATTAGC[C/T]GGGCGTGGTGGCGGG | 54542 |
rs183618862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122899719 | TGGTTTGCAGAGTTA[C/T]ACAAGAAAAGGCCTT | 54542 |
rs183635950 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RC3H2 | GRCh38.p7 | 9:122854772 | TGGTTGTTAAATGGA[G/T]GGAAATGTTTTCCAT | 54542 |
rs183736699 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122889775 | TATCTTGATGGCAAT[G/T]GAAGCTTAAATGAGA | 54542 |
rs183753482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122869754 | TTTGTATTTTTAGTA[A/G]AGATGGGGTTTCATC | 54542 |
rs183808359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122856813 | AAACTTTTCTCAAGT[C/T]GAACTCAGCAGATCG | 54542 |
rs183850896 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | RC3H2 | GRCh38.p7 | 9:122879207 | TTGAGACCAGCCTGG[A/C]CAACATGGTAAAACC | 54542 |
rs184003964 | snp | C/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122890923 | TGAACATTTCCATCA[C/T]TACAGAATAAGAACA | 54542 |
rs184269810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122885100 | GTATATAGTACTGTA[C/T]TGTATCATTAATTTT | 54542 |
rs184274888 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RC3H2 | GRCh38.p7 | 9:122861677 | CAGGAACTCAATACA[C/T]TGCATCTCAACCAGA | 54542 |
rs184277284 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RC3H2 | GRCh38.p7 | 9:122863017 | GGCTGTCCAATTATC[A/G]CCACTAATTCTGAAA | 54542 |
rs184280007 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122894946 | GGTAACAGTAACTAC[A/C]AAAGCCATCACTTGG | 54542 |
rs184300589 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RC3H2 | GRCh38.p7 | 9:122884241 | GAGCTTGCAGTGAGC[C/T]GAGATCGTGCCACCA | 54542 |
rs184340058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RC3H2, SNORD90 | GRCh38.p7 | 9:122881735 | CACAATCTAGGCTCG[C/T]TGTAGCCTTGACTTT | 54542 |
rs184447730 | snp | C/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | RC3H2 | GRCh38.p7 | 9:122905350 | ACCACGGAGGCGGAC[C/G]TGGAGGGATCCCGAT | 54542 |
rs184581749 | snp | A/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122870577 | TGAATTCTTAGTATT[A/G]GGGCAGCTAAAGGCT | 54542 |
rs184596872 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RC3H2 | GRCh38.p7 | 9:122903528 | AAAAATATATGAACA[A/G]AGGACGTAAGTCTTC | 54542 |
rs184685995 | snp | A/G | | | intron-variant, upstream-variant-2KB | RC3H2, SNORD90 | GRCh38.p7 | 9:122880880 | TTTTCAGGGAGGGTG[A/G]GGGATACTTACATAT | 54542 |
rs184768268 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122857503 | CAGCTGAAAGATCTT[C/G]GGCAAATTACTTAAC | 54542 |
rs184774124 | snp | A/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122868217 | GGAGCCCCTCTGCCC[A/G]GCCACCACCCCGTCT | 54542 |
rs184795563 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RC3H2 | GRCh38.p7 | 9:122903917 | TTAAAAAGGAGAATC[C/T]ATTAATATTCTTAAT | 54542 |
rs184808611 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RC3H2, SNORD90 | GRCh38.p7 | 9:122881162 | TACATGAATTGATTT[C/G]TGCACAATAAACAGG | 54542 |
rs184864500 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | RC3H2 | GRCh38.p7 | 9:122850628 | TTTTGTATTTTTGTA[G/T]AGACAGGGTTTCACT | 54542 |
rs185059682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122872371 | ACCTGTGGACCAATA[C/T]AGAAGTTTAACTTGT | 54542 |
rs185102609 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RC3H2 | GRCh38.p7 | 9:122891711 | AATAAATGAATGAAT[A/G]AATACAGGGGATAAG | 54542 |
rs185122116 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RC3H2 | GRCh38.p7 | 9:122876408 | CAAGGCAGGCAGATC[A/G]CTTGAGGTCAGGAGT | 54542 |
rs185241328 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | RC3H2 | GRCh38.p7 | 9:122852652 | GTCAGCTCCCAACCC[A/G]GCCAGCCGCCCTGTC | 54542 |
rs185273188 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RC3H2 | GRCh38.p7 | 9:122896798 | GAGGCTGAGGTGGGC[A/G]GATCACCTGACGTCA | 54542 |
rs185279890 | snp | A/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122861520 | AAAAAGAAAAGAAAA[A/G]AAACCATATATATAT | 54542 |
rs185410027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122861859 | AGGAACTGTGGGTAA[C/T]AAAAGTAGGTACAAA | 54542 |
rs185533434 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | RC3H2 | GRCh38.p7 | 9:122884771 | GGCAGGAGAATCCCT[C/T]GAACCCGGGAGGTGG | 54542 |
rs185564096 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RC3H2, SNORD90 | GRCh38.p7 | 9:122881849 | TTTTTAAGCATAGAA[C/G]TGACATGATCAGATT | 54542 |
rs185580656 | snp | A/C/G | 0.000431328 | 0.0146792 | synonymous-codon | RC3H2 | GRCh38.p7 | 9:122858999 | ATCGGCATATGGCAT[A/C/G]GAAGCAGGTGGGAGG | 54542 |
rs185633195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122889305 | TCACAGGTTATAAAG[A/G]AATATATTCTTTTAT | 54542 |
rs185786747 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | RC3H2 | GRCh38.p7 | 9:122868272 | GAGAACGGGCCATGA[C/T]GACAATTGCGGTTTT | 54542 |
rs186039935 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RC3H2 | GRCh38.p7 | 9:122857796 | ATTCAGTGTTTATTG[A/C]ACTAAACTCAATTGC | 54542 |
rs186080241 | snp | G/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122885352 | CAACTTTTCAGTAAA[G/T]ACGAAATTATTTCAG | 54542 |
rs186086595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122863567 | CTTCAGTACTGTTTC[A/G]TATGTGTAAATGCTG | 54542 |
rs186095195 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant, downstream-variant-500B | RC3H2 | GRCh38.p7 | 9:122853547 | ACTTGAGGTCAGGAG[A/T]TCAAGACCAGCTTAG | 54542 |
rs186129947 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122877123 | TCCCTCAGGCTGGAG[G/T]GCAGTGGTGTGAACA | 54542 |
rs186131952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122898070 | GTGTGAAGAAAACAG[C/T]TTTGCCACCTGAAAG | 54542 |
rs186210274 | snp | G/T | 0.0107246 | 0.0724382 | upstream-variant-2KB | RC3H2 | GRCh38.p7 | 9:122905884 | AGAGTCCAAAGTGGG[G/T]GGGGGAGGGGGGGAA | 54542 |
rs186249471 | snp | C/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122873215 | AAAAGCTCAGAGTGA[C/G]GTAGCAATATGTATT | 54542 |
rs186355463 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | RC3H2 | GRCh38.p7 | 9:122849529 | GTAATATCTTTTTTT[A/T]AAAAAAAATATACAT | 54542 |
rs186391996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122893547 | ACTTAACAGCAGGAG[C/T]TGTGTGGATTAATGA | 54542 |
rs186474530 | snp | C/T | 1.68542e-05 | 0.0029029 | intron-variant | RC3H2 | GRCh38.p7 | 9:122854288 | AGAGAAATATGTTTA[C/T]TGTAATAAAAGTGAA | 54542 |
rs186490241 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RC3H2 | GRCh38.p7 | 9:122898718 | CACGTCATCGCACTC[A/C]AGCCTGGACAAAAAG | 54542 |
rs186533398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122882822 | TCACTACAGAGAATG[A/G]GATAACAAACATAAT | 54542 |
rs186547580 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RC3H2 | GRCh38.p7 | 9:122859476 | TTAAAACACACAACA[A/G]AGCTATTAACAGACG | 54542 |
rs186566433 | snp | C/T | | | upstream-variant-2KB | RC3H2 | GRCh38.p7 | 9:122906949 | ATATACACACATATA[C/T]ACATATATGCACATA | 54542 |
rs186706923 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122877651 | TATTCACTCTAGGAA[C/G]TTCAGAACTTTATAA | 54542 |
rs186772366 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RC3H2 | GRCh38.p7 | 9:122879254 | CAAAAATTAGCAGGG[C/T]GTGGTGGCACTTGCC | 54542 |
rs186822342 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RC3H2 | GRCh38.p7 | 9:122874401 | TGGATAAAAAGCCAC[G/T]GAAGCAGTAAAACCA | 54542 |
rs186822431 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122894892 | CTCAACAACAACAAC[A/C]AAAAAGAAAATGGAG | 54542 |
rs186832101 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RC3H2 | GRCh38.p7 | 9:122850625 | TTTTTTTGTATTTTT[A/G]TAGAGACAGGGTTTC | 54542 |
rs186892471 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122861465 | ATTGCACTCCAGCCC[A/C]GGCAACAAGAGCGAA | 54542 |
rs186928421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122884057 | TCCAGCACTTTGGGA[A/G]GCCAAGGCGGGCGGA | 54542 |
rs186982156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122899754 | GAAGAATGAATTTCA[C/T]CTTAAATCTACTGAA | 54542 |
rs187044329 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RC3H2 | GRCh38.p7 | 9:122863957 | GGTCAGGCTGGTCTT[A/G]AACGCCCAACCTCAG | 54542 |
rs187140076 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RC3H2 | GRCh38.p7 | 9:122864621 | GGCTCCAAAGAGTCC[C/T]CTCCTTTTTTTTTTT | 54542 |
rs187165395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122887662 | TTTTTTAGAAAAACA[A/G]TTGAGTCCGTACTAA | 54542 |
rs187265540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122887015 | TAAAACTTTGTATAA[C/T]GGAAAATTTGCCTCA | 54542 |
rs187419450 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RC3H2 | GRCh38.p7 | 9:122888103 | CATTAACATAATTAT[C/T]TGCTTGCTTGTTTTA | 54542 |
rs187440017 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | RC3H2 | GRCh38.p7 | 9:122903597 | GGGTAACTCAAAGGA[C/T]CCACTAATGAACACG | 54542 |
rs187575849 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122871477 | TAATTTTTTCTGTTT[G/T]TAGTAGAGACGGGGT | 54542 |
rs187601070 | snp | A/G | 8.65209e-05 | 0.0065767 | intron-variant | RC3H2 | GRCh38.p7 | 9:122883418 | GTTCATGACAAATGA[A/G]GAACCCATCAGATCA | 54542 |
rs187778689 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RC3H2 | GRCh38.p7 | 9:122901186 | CTCTTAATAAAAATG[A/T]AAACCTTAGGGCTTA | 54542 |
rs187780834 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RC3H2 | GRCh38.p7 | 9:122879663 | CTTATGAGTCACATA[C/T]GGAGTCCAATTAACA | 54542 |
rs187785217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122855978 | ATTCAGAGGACTTCA[C/T]AGCAAACAATTATAC | 54542 |
rs187875390 | snp | C/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122860795 | CGACAAGTTCTCAAC[C/T]GAAAAAATATAGTCC | 54542 |
rs187952112 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RC3H2 | GRCh38.p7 | 9:122884345 | TGATATGCAAAGGAC[C/T]CACAGTAGGCTTATA | 54542 |
rs188020593 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122850299 | CTGTTTTCCAAAAGT[A/T]ATGATAAAAATTAAA | 54542 |
rs188142726 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | RC3H2 | GRCh38.p7 | 9:122856667 | CTCTGGAGATAAAGG[C/G]GAAATGAATAAATTT | 54542 |
rs188164908 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RC3H2 | GRCh38.p7 | 9:122902886 | AAATAGCTAAAATTA[G/T]TTTTAGTAATATATT | 54542 |
rs188207125 | snp | A/C | | | missense | RC3H2 | GRCh38.p7 | 9:122854044 | TCTGTTGCATGGCCA[A/C]AGCATTGGCCTCTCT | 54542 |
rs188248271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122898186 | TGATTAAGAGAGCTG[C/T]TTGTTCATAAATGAA | 54542 |
rs188248612 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RC3H2 | GRCh38.p7 | 9:122877380 | CCTTAACTTGCATTT[C/T]TGAAAGTCATCACAA | 54542 |
rs188371608 | snp | A/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122868353 | TTGCCGTGTCTGTGT[A/G]GAAAGAAGTAGACAT | 54542 |
rs188415152 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | RC3H2, SNORD90 | GRCh38.p7 | 9:122880392 | CTCACTGCTTTTATG[C/T]TAGTATCATGTATTT | 54542 |
rs188604601 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RC3H2 | GRCh38.p7 | 9:122885187 | AACTAAATACTTTAG[C/T]TTTAAAGTATTAAAA | 54542 |
rs188617513 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RC3H2 | GRCh38.p7 | 9:122863188 | ACCTTTTGTATCTGG[C/T]TTCTTTCATTTAGCA | 54542 |
rs188689417 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RC3H2 | GRCh38.p7 | 9:122869308 | AAGTAATGTTATTAA[A/T]GTTATATATAAACAT | 54542 |
rs188703434 | snp | A/G | 0.0648419 | 0.167978 | intron-variant | RC3H2 | GRCh38.p7 | 9:122866771 | AACCTCCACCTCCCA[A/G]CCACCTGCCTTGGCC | 54542 |
rs188859230 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RC3H2 | GRCh38.p7 | 9:122890117 | CTGCACTCCAGCCTG[C/G]GTGACAGAGTGAGAC | 54542 |
rs188867142 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RC3H2 | GRCh38.p7 | 9:122870257 | GGACATGCCTGTAAT[A/C]CCAGCTACTTGGGAG | 54542 |
rs188891344 | snp | A/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122866711 | TTCACTCAGTGCTCA[A/G]TGGTGCCCAGGCTGG | 54542 |
rs188926304 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RC3H2 | GRCh38.p7 | 9:122894248 | TGGGCGACAGAGCAA[A/G]ACTCCGTCTCAAAAA | 54542 |
rs188932140 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | RC3H2 | GRCh38.p7 | 9:122861690 | CATTGCATCTCAACC[A/C]GATTAGAGGGTTTTT | 54542 |
rs188957930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122889381 | ACGTTTGTAATTTAT[A/G]TAGTTTATAGAGAAT | 54542 |
rs188975117 | snp | C/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122857137 | TGATAACCGTGGAAC[C/T]TGGGTGTTGGGTACA | 54542 |
rs188985171 | snp | A/G | 0.00676609 | 0.0577691 | upstream-variant-2KB | RC3H2 | GRCh38.p7 | 9:122905750 | CGACAGGATCCCTCA[A/G]TCCCTTTACAAAGAT | 54542 |
rs188993344 | snp | A/G/T | 4.96868e-05 | 0.00498411 | missense | RC3H2 | GRCh38.p7 | 9:122858006 | TTGAAGAGACAAGAG[A/G/T]TGCTTTCTGAGTGTG | 54542 |
rs189005668 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RC3H2, SNORD90 | GRCh38.p7 | 9:122880888 | GAGGGTGGGGGATAC[G/T]TACATATCAGACACC | 54542 |
rs189222994 | snp | A/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122873804 | TATAACTATACCATA[A/G]TTTTTATTTATTTAT | 54542 |
rs189227552 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RC3H2 | GRCh38.p7 | 9:122884846 | GACATAGCGAAAGTC[C/T]GTCTCCAAAAAAAAA | 54542 |
rs189230364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122857508 | GAAAGATCTTGGGCA[A/G]ATTACTTAACTTCTG | 54542 |
rs189254271 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RC3H2 | GRCh38.p7 | 9:122904267 | ATAAATAAATCACTG[C/G]ATTAGATTTACTTTA | 54542 |
rs189273694 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | RC3H2, SNORD90 | GRCh38.p7 | 9:122881557 | AAAAAGCAGAGCACA[C/T]AGGGTTAAGATATGA | 54542 |
rs189275405 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | RC3H2, SNORD90 | GRCh38.p7 | 9:122881775 | AGCAATCCTCTCGCT[C/T]TGGCCTCCCAAAGTG | 54542 |
rs189483344 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RC3H2 | GRCh38.p7 | 9:122875768 | GAAAGAGCACAGTGC[A/G]TACCACAAACTGAGA | 54542 |
rs189500228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122876521 | TGGTTCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 54542 |
rs189502469 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | RC3H2 | GRCh38.p7 | 9:122853414 | AAAAATACTGATTTT[A/G]TACCTGTGGAACCTG | 54542 |
rs189528007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122861867 | TGGGTAATAAAAGTA[A/G]GTACAAACGTAAGGG | 54542 |
rs189562682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122872576 | ACATCTTGAATAGTA[A/G]CCAGTATATAATAAT | 54542 |
rs189563741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122892198 | CTCACTGCAGCCTCA[A/G]CTTCCTGGGCTCATG | 54542 |
rs189763302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122850884 | TTTATCTCAACAAAA[A/G]GCAAGTTTCAGGCTA | 54542 |
rs189787537 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122896254 | GGAGAATTTATTACT[C/G]ACACATTGGTTTTTG | 54542 |
rs190044487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122890940 | ACAGAATAAGAACAA[A/G]TATGCTGTTATTTCA | 54542 |
rs190060816 | snp | C/T | 0 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122864912 | TACAGGTGTGAACCA[C/T]TGCACCCGGCCAAGT | 54542 |
rs190105390 | snp | C/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122887789 | TTGCTCTTTCACCCA[C/G]GCTAAAGTGAAGTGG | 54542 |
rs190299148 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RC3H2 | GRCh38.p7 | 9:122870845 | TGGTAAAAGCTCAAT[C/T]CAATTCTTTACTTAT | 54542 |
rs190312057 | snp | C/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122871675 | CTATCTAAGAGATCT[C/T]CCCTTTCTCAATCAC | 54542 |
rs190471451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122879351 | GTGAGCTGAGATAGC[A/G]TCACTGCACTCCAGC | 54542 |
rs190476091 | snp | C/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122900234 | AATACCTTTAAGATA[C/T]AAAGGTAAAACACTG | 54542 |
rs190489673 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | RC3H2 | GRCh38.p7 | 9:122855022 | TGGGAGGCTGAGGCA[A/G]GAGAATCGCTTGAAC | 54542 |
rs190601630 | snp | A/G | 0 | 0 | intron-variant | RC3H2 | GRCh38.p7 | 9:122891258 | AAATTCCTGACCCCA[A/G]ATGATCTGCCCGCCT | 54542 |
rs190619618 | snp | C/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122860976 | GCTCCTGGAACAGAG[C/T]AGGCACTTGGTAAAT | 54542 |
rs190717127 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RC3H2 | GRCh38.p7 | 9:122906559 | AAGAAGAAAAAAAAT[A/G]ACCATGACTTGTAAT | 54542 |
rs190719155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RC3H2, SNORD90 | GRCh38.p7 | 9:122882029 | AGGAGTTCAAGGCTG[C/T]AGTGAACTATGATGG | 54542 |
rs190724016 | snp | A/C | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122859165 | AACATTTTATAATGG[A/C]TTAAATCTAAGGCAG | 54542 |
rs190868279 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RC3H2 | GRCh38.p7 | 9:122883737 | TGTAAATCCCAGCAC[A/G]TTGAGAGGCCGAGGC | 54542 |
rs190894989 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RC3H2 | GRCh38.p7 | 9:122887067 | ATCAGTGGGTTCAGA[C/T]TTTATCCATCTGCTA | 54542 |
rs191026526 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | RC3H2 | GRCh38.p7 | 9:122907174 | CAAGGAATTCTCCTG[C/G]CTTAGCCTCCCCAGT | 54542 |
rs191115597 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122864074 | ATCTCCCCCATCATG[G/T]GCTGACTGCAGAAGT | 54542 |
rs191145992 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122877771 | CATAACCCTGAATTG[C/G]CACTTCAGATATTCC | 54542 |
rs191283369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122894903 | CAACAAAAAAGAAAA[C/T]GGAGACAGACTGAAC | 54542 |
rs191285569 | snp | A/G | 0.000197804 | 0.00994299 | intron-variant | RC3H2 | GRCh38.p7 | 9:122875135 | ATATAGAACTAGTTC[A/G]ATTGGGTACAAACAG | 54542 |
rs191352688 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | RC3H2 | GRCh38.p7 | 9:122854770 | CATGGTTGTTAAATG[C/G]AGGGAAATGTTTTCC | 54542 |
rs191376120 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | RC3H2 | GRCh38.p7 | 9:122898979 | CAAATATATTAGTTC[A/C]ACAGAAATTAGATGT | 54542 |
rs191387671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122863612 | TCATAAATCCCTTAA[A/G]AGCAAAGTATCTTGT | 54542 |
rs191535849 | snp | C/T | 0.00232003 | 0.0339799 | intron-variant, downstream-variant-500B | RC3H2, SNORD90 | GRCh38.p7 | 9:122879954 | TATTCACCTCAAAAG[C/T]AGAAAAAAATATAAG | 54542 |
rs191563512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122869343 | TAATTAAATATAAAG[C/T]GTTAGTAGTAAGCAA | 54542 |
rs191567876 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RC3H2 | GRCh38.p7 | 9:122901222 | TCTAATTAAAACCAT[C/T]GTTTTCATTCTTGTT | 54542 |
rs191637312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122886317 | CACTTGATGGACATT[C/T]GGATTGTTTCCACCT | 54542 |
rs191663087 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RC3H2 | GRCh38.p7 | 9:122850013 | ACAGAGTCTCCCTCC[A/G]TCGCCCAGGCTGGAG | 54542 |
rs191695138 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RC3H2 | GRCh38.p7 | 9:122893624 | TTCTTGGTGTTGGAT[A/G]TTAACATTAGGTTAA | 54542 |
rs191789437 | snp | A/G | 3.31268e-05 | 0.00406968 | synonymous-codon | RC3H2 | GRCh38.p7 | 9:122890393 | GGTTCTGGTGCTGTA[A/G]TATCAGTTCTGTTAC | 54542 |
rs191934905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122882966 | AAGTTTACCAAATGA[C/T]TTCCTTATGTTCTTT | 54542 |
rs191942082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122857481 | GGATTCATATCCCAG[C/T]TATTTACAGCTGAAA | 54542 |
rs191979120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122903817 | ACCTCTATTTCTTCA[A/G]AAATTGAACGTGGAA | 54542 |
rs191983174 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RC3H2, SNORD90 | GRCh38.p7 | 9:122881047 | CTTGTAAGTAGAAAA[G/T]TATAGTAAAAGTTAT | 54542 |
rs192007711 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RC3H2 | GRCh38.p7 | 9:122873261 | ACAGTCACATCACCT[A/C]CTTTTCTAATCCTTT | 54542 |
rs192204371 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RC3H2 | GRCh38.p7 | 9:122861466 | TTGCACTCCAGCCCA[A/G]GCAACAAGAGCGAAA | 54542 |
rs192237563 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | RC3H2 | GRCh38.p7 | 9:122884130 | AAACCCCGCCTCTAC[C/T]AAAAATACAAAAATT | 54542 |
rs192258415 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RC3H2 | GRCh38.p7 | 9:122859799 | AAGGAAAAAAACTTA[A/T]GAGTCACATAGTCAA | 54542 |
rs192432972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122856034 | TGTAATAAGCAAGAA[A/G]TGGTATTTTTACAAT | 54542 |
rs192446895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122889774 | CTATCTTGATGGCAA[C/T]TGAAGCTTAAATGAG | 54542 |
rs192507817 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | RC3H2 | GRCh38.p7 | 9:122894342 | CACAGTTATAGGTAC[C/G]AGGGATATATCAATG | 54542 |
rs192512789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122873930 | TCAAGCCATTCTCCC[A/G]CCTCAGCCTCCCGAG | 54542 |
rs192514301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122850310 | AAGTTATGATAAAAA[C/T]TAAAATACTAGTTAG | 54542 |
rs192551929 | snp | A/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122867035 | GTCTGGGATGTGAGG[A/G]GCGCCTCTGCCTGGC | 54542 |
rs192591197 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RC3H2 | GRCh38.p7 | 9:122850627 | TTTTTGTATTTTTGT[A/G]GAGACAGGGTTTCAC | 54542 |
rs192691522 | snp | A/G | 4.97442e-05 | 0.00498695 | synonymous-codon, upstream-variant-2KB | RC3H2, SNORD90 | GRCh38.p7 | 9:122880603 | ACAAACCTTATCAAT[A/G]ATAGACTGCATGTGT | 54542 |
rs192904886 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RC3H2 | GRCh38.p7 | 9:122856804 | AAAGTTAAAAAACTT[C/T]TCTCAAGTCGAACTC | 54542 |
rs192919941 | snp | A/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122902897 | ATTATTTTTAGTAAT[A/G]TATTTTATTTATCCC | 54542 |
rs192972774 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RC3H2 | GRCh38.p7 | 9:122851866 | CTCCACCTCCCAGCC[A/G]CCTGCCTTGGCCTCC | 54542 |
rs192984196 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RC3H2 | GRCh38.p7 | 9:122896412 | ACATTTCTTTTCATA[C/T]CACCTGGTGAATAAA | 54542 |
rs193045190 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RC3H2 | GRCh38.p7 | 9:122888318 | TATTTTTAGGTATTA[C/T]TTTGATCATTTTTAA | 54542 |
rs193102879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122884588 | CTGGGCACGCTGGCT[C/T]ATGCTTGTAATCCCA | 54542 |
rs193185961 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RC3H2 | GRCh38.p7 | 9:122876092 | AAGGATGGAAAGAAG[A/G]ATAAAGAACTGAGAA | 54542 |
rs199502221 | snp | A/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122859869 | TCATTCATTTATCTA[A/T]AGGAAACAATGTTTC | 54542 |
rs199513585 | snp | A/C/G | 6.6331e-05 | 0.00575862 | intron-variant | RC3H2 | GRCh38.p7 | 9:122854124 | AAAAGTTAGCTTCCA[A/C/G]CTATAGCTTTCAACT | 54542 |
rs199544020 | snp | C/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122878465 | TTAGTAGAGATGGGG[C/T]TTCACCATGTTAGCC | 54542 |
rs199553774 | snp | A/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122861515 | AAAAAAAAAAGAAAA[A/G]AAAAAAAACCATATA | 54542 |
rs199593875 | snp | A/G | 0.00197185 | 0.0313374 | synonymous-codon, downstream-variant-500B | RC3H2, SNORD90 | GRCh38.p7 | 9:122880038 | CTAAATGAGGCCTCA[A/G]TCTATTTAAGTTAGC | 54542 |
rs199608083 | snp | A/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122865910 | ATATGTATTTTTTTT[A/G]CCCCTCATGCCACTT | 54542 |
rs199639103 | snp | C/T | 8.28233e-05 | 0.00643465 | intron-variant | RC3H2 | GRCh38.p7 | 9:122859914 | TTGTCTAAAATTACT[C/T]ACCTGTCTGTGGGTA | 54542 |
rs199650380 | in-del | -/CT | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122866452 | TCTCCCTCTGATGCC[-/CT]GAGCCGAAGCTGGAC | 54542 |
rs199665420 | in-del | -/AAAT | 0.001736 | 0.0294106 | intron-variant | RC3H2 | GRCh38.p7 | 9:122855891 | GAACTGGTTAAAAAA[-/AAAT]AAATAAAGCCAATTA | 54542 |
rs199700970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122862808 | GCTGAGGCAGGAGAA[C/T]TGCTTGAACCTGGCA | 54542 |
rs199701630 | snp | A/C | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122864361 | TCTTATGCTGACACT[A/C]AGTAACAATTAATGG | 54542 |
rs199724802 | in-del | -/TAAAG | 0.00716266 | 0.059414 | intron-variant | RC3H2 | GRCh38.p7 | 9:122869291 | ATAATTATATATGCC[-/TAAAG]TAATGTTATTAATGT | 54542 |
rs199726498 | in-del | -/TTT | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122860406 | ACCATTTACCCATTC[-/TTT]TTTTTTTTTTTTTTT | 54542 |
rs199744100 | snp | C/T | 0.00199806 | 0.0315443 | intron-variant, downstream-variant-500B | RC3H2, SNORD90 | GRCh38.p7 | 9:122879742 | CAGTCAGAAATGTAA[C/T]AAATGTACTTACCTG | 54542 |
rs199763632 | snp | A/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122849845 | AAAAGAAATGACATT[A/T]AAAACAAATTAGCTT | 54542 |
rs199828711 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RC3H2 | GRCh38.p7 | 9:122861942 | AAAGTAAAATAGAGA[C/G]AACAAGGAAAATGAT | 54542 |
rs199859915 | snp | C/T | | | intron-variant, downstream-variant-500B | RC3H2 | GRCh38.p7 | 9:122853398 | AAAATCAGTATTTTT[C/T]TTTTTTTTTTTTTTT | 54542 |
rs199901510 | snp | C/G/T | 0.00071185 | 0.0188528 | missense | RC3H2 | GRCh38.p7 | 9:122859980 | CTTGAAAATACTGAA[C/G/T]GTTTTCAGAATGCGG | 54542 |
rs199919087 | snp | A/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122867713 | CGCCTCTGCCTGGCC[A/G]CGACCCCGTCTGGGA | 54542 |
rs199925809 | snp | A/G | | | downstream-variant-500B | RC3H2 | GRCh38.p7 | 9:122848964 | AACAAAGCAGAAACT[A/G]CTCTTGAAAAATGGA | 54542 |
rs199957618 | snp | C/G | 0.00199792 | 0.0315431 | missense | RC3H2 | GRCh38.p7 | 9:122858695 | GCACAGTTGTCCTTG[C/G]CTCACTTGGTGGCTG | 54542 |
rs199983507 | in-del | -/T | 0.0158469 | 0.0875917 | intron-variant | RC3H2 | GRCh38.p7 | 9:122886811 | GCTTGTTAGTCATCG[-/T]TGTCTCTTCTTTGGA | 54542 |
rs199990103 | snp | C/T | 0.00145728 | 0.026954 | missense | RC3H2 | GRCh38.p7 | 9:122858670 | GCATCTTCACTTACC[C/T]TTGGTAAAGGCACAG | 54542 |
rs200051138 | snp | A/G | | | intron-variant, upstream-variant-2KB | RC3H2, SNORD90 | GRCh38.p7 | 9:122881478 | AAAAAAAAAAAAAAG[A/G]AAAAAAGAGAAGGGG | 54542 |
rs200090982 | snp | C/G/T | 0.000298087 | 0.012205 | missense | RC3H2 | GRCh38.p7 | 9:122857991 | TTGCCACAGGAAGAG[C/G/T]TGAAGAGACAAGAGG | 54542 |
rs200112699 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122860434 | TTTTTTTGAGACAGG[G/T]TGTCACTCTGTCACC | 54542 |
rs200119402 | snp | G/T | 6.62482e-05 | 0.00575497 | synonymous-codon | RC3H2 | GRCh38.p7 | 9:122855299 | CCATTTTGAGATGAT[G/T]GGTCCATCACTAAAG | 54542 |
rs200131645 | in-del | -/TTT | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122869561 | GGCCAGTTTACACGA[-/TTT]TTTTTTTTTTTTTTT | 54542 |
rs200225032 | in-del | -/G | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | RC3H2, SNORD90 | GRCh38.p7 | 9:122882142 | GAGAAATTATCATCA[-/G]GGGTATTTACATAGC | 54542 |
rs200237353 | snp | C/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122890724 | TAGTAATAAGAAGCC[C/T]AATTTTTAGCTACTT | 54542 |
rs200263633 | snp | C/T | 0.00299542 | 0.0385842 | intron-variant | RC3H2 | GRCh38.p7 | 9:122875350 | ACAACAATGAAGATA[C/T]AGTCCACGGGGGTTA | 54542 |
rs200267058 | snp | A/C | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122850434 | TTATATGCTATCTAT[A/C]TATAGATAGATAGAT | 54542 |
rs200340195 | snp | A/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122861510 | AAAAAAAAAAAAAAA[A/G]AAAAGAAAAAAAACC | 54542 |
rs200342405 | snp | A/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122869530 | GAAGTAACAGAATAT[A/T]AAAAAAACAGGTGAT | 54542 |
rs200390999 | snp | A/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122892658 | TCTTGTGATCCGCCC[A/G]CGCTGGCCTCCCAAA | 54542 |
rs200430732 | snp | C/T | 8.41999e-05 | 0.0064879 | missense | RC3H2 | GRCh38.p7 | 9:122859033 | GACTCTGGAACGTTA[C/T]TGGACCTCACAAAGC | 54542 |
rs200431924 | in-del | -/A | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122894271 | TCAAAAAAAAAAAAA[-/A]GTTCAATGCAATTCA | 54542 |
rs200484277 | in-del | -/C | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122867372 | GAAGTGAGGAGACCC[-/C]TCTGCCCAGCCAGCC | 54542 |
rs200553907 | snp | A/T | | | intron-variant, downstream-variant-500B | RC3H2 | GRCh38.p7 | 9:122853378 | CCCAAGAATGATCAA[A/T]AAAAAAAAAAAAAAA | 54542 |
rs200566131 | snp | A/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122849846 | AAAGAAATGACATTA[A/T]AAACAAATTAGCTTT | 54542 |
rs200582531 | snp | C/T | 0.00199802 | 0.0315439 | missense | RC3H2 | GRCh38.p7 | 9:122859938 | GTGGGTACTGTGGGA[C/T]TTCAAAGGGTATCTG | 54542 |
rs200605645 | snp | C/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122874542 | TATATTTTTGAGACA[C/G]AGTCTTGCTCTGCTG | 54542 |
rs200607307 | in-del | -/A | 0.443195 | 0.158668 | intron-variant | RC3H2 | GRCh38.p7 | 9:122902849 | GAGAGAGACTGTCTC[-/A]AAAAAAAAAAAAAAA | 54542 |
rs200619819 | snp | A/G | 0.000331329 | 0.0128668 | missense | RC3H2 | GRCh38.p7 | 9:122854573 | GCCTCGTTGCCATAT[A/G]AACTCCACCTTGAAT | 54542 |
rs200698071 | in-del | -/A | | | upstream-variant-2KB | RC3H2 | GRCh38.p7 | 9:122906537 | AGACTCCGTCTCAAC[-/A]AAAAAAAAGAAGAAA | 54542 |
rs200704130 | in-del | -/A | 0.0197687 | 0.0974348 | intron-variant | RC3H2 | GRCh38.p7 | 9:122856813 | AACTTTTCTCAAGTC[-/A]GAACTCAGCAGATCG | 54542 |
rs200734101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122855478 | TATCAAAAGACATGT[A/G]ATTAGGTTTTTTGGT | 54542 |
rs200819569 | in-del | -/T | 0.0894459 | 0.191631 | intron-variant | RC3H2 | GRCh38.p7 | 9:122891186 | ACCACACCTGGCTAA[-/T]TTTTTTTTGTATTTT | 54542 |
rs200840595 | snp | A/C/T | 1.65625e-05 | 0.00287766 | synonymous-codon, missense | RC3H2 | GRCh38.p7 | 9:122851119 | ACTCTGTTTCTTCTG[A/C/T]TTTGGTGGCTCCTTT | 54542 |
rs200853537 | snp | A/G | 0.000235905 | 0.010858 | intron-variant, nc-transcript-variant | RC3H2, SNORD90 | GRCh38.p7 | 9:122880215 | CAACATATTTAATAC[A/G]TTTTCAAGTGTCTTC | 54542 |
rs200856968 | snp | C/T | 0.000812516 | 0.0201395 | intron-variant | RC3H2 | GRCh38.p7 | 9:122892881 | ACCAAGTCCTACTTA[C/T]CAGTAAAAATGCATT | 54542 |
rs200902178 | snp | C/T | 1.65658e-05 | 0.00287795 | missense | RC3H2 | GRCh38.p7 | 9:122858955 | GGAGAAGAATTCATT[C/T]GATCTCGAGGGGAAA | 54542 |
rs200904069 | in-del | -/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122892421 | ACCCAGCTTGAATTC[-/T]TTTTTTTTTGAGACA | 54542 |
rs200933994 | in-del | -/GGAT | 0.0166325 | 0.0896639 | intron-variant | RC3H2 | GRCh38.p7 | 9:122864893 | CCTCCAAAAGTGCTG[-/GGAT]TACAGGTGTGAACCA | 54542 |
rs200964914 | snp | G/T | 3.31208e-05 | 0.00406931 | missense | RC3H2 | GRCh38.p7 | 9:122860032 | TAGAAATGGGCTGGA[G/T]TTTTGAGGCACAGAA | 54542 |
rs200992332 | snp | C/G | 5.02155e-05 | 0.00501051 | intron-variant | RC3H2 | GRCh38.p7 | 9:122854641 | GTAGAATGAAACAAT[C/G]GTCAAAAAAGTGAAA | 54542 |
rs201049821 | snp | A/C/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122849850 | AAATGACATTAAAAA[A/C/G]AAATTAGCTTTAAGT | 54542 |
rs201150094 | in-del | -/T | 0.046775 | 0.145601 | intron-variant | RC3H2 | GRCh38.p7 | 9:122884037 | GGTGGCTCACGTCTG[-/T]TAATTCCAGCACTTT | 54542 |
rs201196565 | in-del | -/A | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122865901 | GCCGAGTTTATATGT[-/A]TTTTTTTTTCCCCTC | 54542 |
rs201218160 | snp | G/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122894512 | ACTGGAAATACTAGC[G/T]AGGGGTTACAAATTT | 54542 |
rs201264247 | snp | G/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122850435 | TATATGCTATCTATC[G/T]ATAGATAGATAGATA | 54542 |
rs201421879 | snp | A/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122861514 | AAAAAAAAAAAGAAA[A/G]GAAAAAAAACCATAT | 54542 |
rs201428234 | in-del | -/G | 0.119978 | 0.213528 | intron-variant, downstream-variant-500B | RC3H2 | GRCh38.p7 | 9:122853394 | AAAAAAAAAAAAAAA[-/G]AAAGAAAAATACTGA | 54542 |
rs201440012 | snp | C/T | 4.9894e-05 | 0.00499445 | missense | RC3H2 | GRCh38.p7 | 9:122849761 | AACTTGCATTGCTAA[C/T]AGACACTGGGAGTGG | 54542 |
rs201442234 | in-del | -/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122899089 | ATTAGCCTTTATTGT[-/G]GTTTTTTTTTTTTTT | 54542 |
rs201447680 | snp | A/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122884239 | TGGAGCTTGCAGTGA[A/G]CCGAGATCGTGCCAC | 54542 |
rs201451474 | in-del | -/A | 0.030278 | 0.119257 | upstream-variant-2KB | RC3H2 | GRCh38.p7 | 9:122907067 | TACATATATGTACAT[-/A]TTTTTTTTTTTGAGA | 54542 |
rs201451895 | snp | C/G | 0.000696333 | 0.0186462 | intron-variant | RC3H2 | GRCh38.p7 | 9:122854122 | AGAAAAGTTAGCTTC[C/G]AACTATAGCTTTCAA | 54542 |
rs201462653 | snp | C/T | 3.33946e-05 | 0.00408609 | missense | RC3H2 | GRCh38.p7 | 9:122890543 | GGTTCAAGCTAGCTA[C/T]ACCTTTAGGAAAAGG | 54542 |
rs201463826 | in-del | -/AC | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122849849 | GAAATGACATTAAAA[-/AC]AAATTAGCTTTAAGT | 54542 |
rs201529893 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RC3H2 | GRCh38.p7 | 9:122869655 | GCAACCTCTGCTTCC[C/T]GGGTTCAAGCAATTC | 54542 |
rs201602026 | in-del | -/AAAT | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122868742 | AGAATGATCAATAAA[-/AAAT]AAATAAATAAATAAA | 54542 |
rs201603532 | snp | A/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122849844 | AAAAAGAAATGACAT[A/T]AAAAACAAATTAGCT | 54542 |
rs201671150 | snp | A/G/T | 1.6574e-05 | 0.00287867 | stop-gained, synonymous-codon | RC3H2 | GRCh38.p7 | 9:122892955 | TGCCAAATCCTCAAC[A/G/T]CATTTCTTTGCAACC | 54542 |
rs201677042 | snp | A/G | 3.314e-05 | 0.00407049 | synonymous-codon | RC3H2 | GRCh38.p7 | 9:122858064 | TCTTATCTGCTCCTC[A/G]CAACTGGTCTTCAAA | 54542 |
rs201701811 | snp | C/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122851949 | AGGAGCGTCTCTGCC[C/T]GGCCGCCCATCGTCT | 54542 |
rs201724448 | in-del | -/TTTTG | 0.0221141 | 0.102801 | intron-variant | RC3H2 | GRCh38.p7 | 9:122885868 | TTCATTTAACGTGTT[-/TTTTG]TTTTGTTTTGTTTTG | 54542 |
rs201732933 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | RC3H2 | GRCh38.p7 | 9:122864897 | CAAAAGTGCTGGGAT[C/T]ACAGGTGTGAACCAC | 54542 |
rs201755996 | snp | C/T | 0.000417101 | 0.0144353 | intron-variant | RC3H2 | GRCh38.p7 | 9:122857917 | AGTAATTAAAACCTT[C/T]CTTACATCCGCACGA | 54542 |
rs201791439 | snp | A/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122868839 | AATATTCCCTCCTAT[A/G]TGTGTGTGTGTGTGT | 54542 |
rs201811922 | snp | C/T | | | splice-acceptor-variant | RC3H2 | GRCh38.p7 | 9:122854268 | CAATGAATCTGTCCC[C/T]TTAAAGAGAAATATG | 54542 |
rs201851354 | snp | A/G | 0.00012275 | 0.00783325 | missense | RC3H2 | GRCh38.p7 | 9:122859094 | CCGTTGGAGGTGGTG[A/G]ATAGTATCCTTGAAA | 54542 |
rs201852484 | snp | C/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122864359 | AATCTTATGCTGACA[C/G]TCAGTAACAATTAAT | 54542 |
rs201857025 | snp | C/T | 0.000800659 | 0.0199929 | intron-variant | RC3H2 | GRCh38.p7 | 9:122854525 | TAGAATTAAGAAGAA[C/T]GTTACCTTTCAACAT | 54542 |
rs201858192 | snp | A/C | 0.000132666 | 0.00814341 | missense, downstream-variant-500B | RC3H2, SNORD90 | GRCh38.p7 | 9:122880026 | TTGCAAGAAGCTCTA[A/C]ATGAGGCCTCAGTCT | 54542 |
rs201882331 | snp | A/T | 0.00106052 | 0.0230029 | missense | RC3H2 | GRCh38.p7 | 9:122858078 | CGCAACTGGTCTTCA[A/T]ATGACCACAAGGTTC | 54542 |
rs201911666 | in-del | -/CAAAA | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122870416 | AAACAAACAAACAAA[-/CAAAA]AAAAAAACAACAAAC | 54542 |
rs201912798 | snp | A/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122898768 | AAAAAAAAAAAAAGT[A/T]CCATAAGTTTAGTAA | 54542 |
rs201920127 | snp | A/G | 0.000811534 | 0.0201273 | missense | RC3H2 | GRCh38.p7 | 9:122851364 | GTTCATCAGTATCAA[A/G]TGCTGAAAGCTCTAA | 54542 |
rs201957840 | in-del | -/TAAGA | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122893792 | ACTATATTATTTACT[-/TAAGA]TAAGCATTATTAAGA | 54542 |
rs201964621 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122874260 | GGCAGAGTAGAGCTA[C/G]AGGATAAAATCAGGA | 54542 |
rs202046791 | in-del | -/CA | 0.0193772 | 0.0965046 | intron-variant | RC3H2 | GRCh38.p7 | 9:122891862 | GCAGTGATAAAATTT[-/CA]GTTTTGTCATAGACT | 54542 |
rs202078403 | snp | C/G | 1.65619e-05 | 0.00287762 | synonymous-codon | RC3H2 | GRCh38.p7 | 9:122883225 | ACAAGAAGCTCGATA[C/G]AGTAGTTGCACAACA | 54542 |
rs202108667 | in-del | -/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122878924 | TATTTTTTTTTTTTT[-/T]AGTAGAGATGGGGTT | 54542 |
rs202137617 | in-del | -/A | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122877932 | ATTTTAAAAAGCATT[-/A]AAAAAAAAACCAAAA | 54542 |
rs202205526 | snp | A/C | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122849852 | ATGACATTAAAAACA[A/C]ATTAGCTTTAAGTGC | 54542 |
rs202209622 | snp | A/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122861415 | GAATCGCTTGAACCC[A/G]GGAGGCGGAGGTTGT | 54542 |
rs367546994 | snp | A/G | 8.3053e-05 | 0.00644357 | synonymous-codon | RC3H2 | GRCh38.p7 | 9:122855804 | TATACAGGAGCCTAT[A/G]GTGCCACAAGACCAG | 54542 |
rs367552001 | snp | A/G | 0.00018219 | 0.00954263 | synonymous-codon, upstream-variant-2KB | RC3H2, SNORD90 | GRCh38.p7 | 9:122880735 | TCTGCGTAATGCTTC[A/G]TAACTCCGAAATTCC | 54542 |
rs367554344 | snp | A/T | 0.000132547 | 0.00813977 | intron-variant | RC3H2 | GRCh38.p7 | 9:122851309 | CCTCTCAATTATCTA[A/T]TTGTGGCACTTACTT | 54542 |
rs367745578 | snp | A/G | 1.65965e-05 | 0.00288062 | synonymous-codon, downstream-variant-500B | RC3H2, SNORD90 | GRCh38.p7 | 9:122879847 | CCATTGCATTTTCCA[A/G]CTGCTCCCAAGTTGG | 54542 |
rs367763071 | snp | C/T | 3.37262e-05 | 0.00410633 | intron-variant | RC3H2 | GRCh38.p7 | 9:122854291 | GAAATATGTTTATTG[C/T]AATAAAAGTGAAGTG | 54542 |
rs367770760 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RC3H2 | GRCh38.p7 | 9:122889425 | AATTTTGCTTTTTCC[A/G]CATTTTGATCTAGTT | 54542 |
rs367772642 | snp | A/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122872554 | TGTTCCTCTTTTTCC[A/G]TTAGAAACATCTTGA | 54542 |
rs367857309 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RC3H2 | GRCh38.p7 | 9:122850401 | ATGGCAGTATTATAG[C/G]CAAGAAAATATACTA | 54542 |
rs367977566 | snp | C/G | 1.6566e-05 | 0.00287797 | intron-variant | RC3H2 | GRCh38.p7 | 9:122851070 | TTATGAATTTTCTGT[C/G]TAACACTCACAGAAT | 54542 |
rs367978296 | snp | C/T | 4.63017e-05 | 0.00481131 | intron-variant | RC3H2 | GRCh38.p7 | 9:122855928 | AGAAGCTTAAATTTA[C/T]AAGCTTGTAACTAAT | 54542 |
rs367984525 | snp | A/T | 1.65622e-05 | 0.00287764 | synonymous-codon | RC3H2 | GRCh38.p7 | 9:122883213 | GCTTACCTTAAAACA[A/T]GAAGCTCGATACAGT | 54542 |
rs368031137 | snp | A/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122901960 | TTGAGACGGAGTTTC[A/G]CTCTTGTTGCCCAGG | 54542 |
rs368034443 | snp | C/T | 0.000165714 | 0.00910107 | intron-variant | RC3H2 | GRCh38.p7 | 9:122859899 | CTTTTTTTCTTAGAA[C/T]TGTCTAAAATTACTC | 54542 |
rs368068992 | snp | C/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122886523 | TGCCCACATTCTCCA[C/T]GTTCTCATCAACATT | 54542 |
rs368137870 | snp | A/G | 0.0659589 | 0.169201 | intron-variant | RC3H2 | GRCh38.p7 | 9:122868551 | GAAGGCAGCATGCTC[A/G]TTAAGAGTCATCACC | 54542 |
rs368188732 | snp | C/T | 0.000132474 | 0.00813755 | missense | RC3H2 | GRCh38.p7 | 9:122858794 | AGTGCATCACATCCA[C/T]TGGAGGTAAAGAATT | 54542 |
rs368233765 | snp | A/G/T | 0.000258817 | 0.011373 | utr-variant-5-prime | RC3H2 | GRCh38.p7 | 9:122897528 | GGAAGCTGGATGCTC[A/G/T]GGTTAGCAGTCTAGC | 54542 |
rs368311110 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | RC3H2, SNORD90 | GRCh38.p7 | 9:122881159 | AGCTACATGAATTGA[C/T]TTGTGCACAATAAAC | 54542 |
rs368338346 | snp | C/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122855550 | CTACCAGTAAACCAC[C/T]AATGTTCAAATAACT | 54542 |
rs368341694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122872881 | ATGAGCCACTGCTCC[C/T]GGCCACTATTTGTTG | 54542 |
rs368432643 | snp | G/T | 0.000167986 | 0.00916323 | missense | RC3H2 | GRCh38.p7 | 9:122851226 | GCTGTATGTCCAAGA[G/T]CTCCTAAGAAAATAA | 54542 |
rs368437387 | snp | A/G | 9.93591e-05 | 0.00704767 | missense | RC3H2 | GRCh38.p7 | 9:122859994 | ATGTTTTCAGAATGC[A/G]GAGGATATACTGGTA | 54542 |
rs368450256 | snp | C/T | 0.000101313 | 0.00711661 | intron-variant | RC3H2 | GRCh38.p7 | 9:122855683 | TACAACATGAGTGAA[C/T]ATGCATCATCTCTCA | 54542 |
rs368450588 | snp | A/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122874420 | GCAGTAAAACCAACT[A/G]GATTACCATGTGAAA | 54542 |
rs368489458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122887161 | CCATTAATACATTTG[A/G]GGATGTAAAATTGTG | 54542 |
rs368498527 | in-del | -/G | 0.00318978 | 0.0398085 | intron-variant | RC3H2 | GRCh38.p7 | 9:122866211 | ATAGTTCTCAGAATA[-/G]TTTATACCTAAAGTT | 54542 |
rs368522951 | snp | A/T | | | intron-variant, upstream-variant-2KB | RC3H2, SNORD90 | GRCh38.p7 | 9:122882094 | AGTCTGTTGCTTTAA[A/T]AAAAAAATGAAAAGA | 54542 |
rs368619805 | snp | C/G | 3.50257e-05 | 0.00418469 | intron-variant, downstream-variant-500B | RC3H2, SNORD90 | GRCh38.p7 | 9:122879729 | TTAGAGACAACAGCA[C/G]TCAGAAATGTAATAA | 54542 |
rs368626618 | snp | C/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122850535 | ACTGTCTCCGCCTCC[C/T]GGGTTCAAGCGATTC | 54542 |
rs368701278 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RC3H2 | GRCh38.p7 | 9:122857559 | ATATGGAAAATACCT[A/G]CCCCCTAAGGTTTTT | 54542 |
rs368720900 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RC3H2 | GRCh38.p7 | 9:122871320 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCGCTCTGT | 54542 |
rs368737774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122895066 | CACTGTAAAGACCTG[C/T]AGGCAATTTAAGAAC | 54542 |
rs368781093 | snp | A/C/G | 0.00318978 | 0.0398085 | intron-variant | RC3H2 | GRCh38.p7 | 9:122864770 | GGACTACATATGCCC[A/C/G]CCACCATGCCCGGCT | 54542 |
rs368794916 | snp | C/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122901667 | TGCGATTTCGGCTCA[C/G]TGCAACCTCCGCCTC | 54542 |
rs368821339 | snp | C/T | 1.66857e-05 | 0.00288835 | missense | RC3H2 | GRCh38.p7 | 9:122854228 | CCAGTACTGGAATGC[C/T]TTCTATGACCAGATA | 54542 |
rs368828068 | snp | A/C/T | 3.31647e-05 | 0.00407201 | missense | RC3H2 | GRCh38.p7 | 9:122857930 | TTTCTTACATCCGCA[A/C/T]GAAAGTCTACACTGA | 54542 |
rs368862485 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RC3H2 | GRCh38.p7 | 9:122851641 | GCCTGCAATTGCAGG[C/T]GCGCGCCGCCACGCC | 54542 |
rs368898041 | in-del | -/CT | | | intron-variant, upstream-variant-2KB | RC3H2, SNORD90 | GRCh38.p7 | 9:122880334 | TATAAGCTGTATTAA[-/CT]CTCTGAGGTCAGAAT | 54542 |
rs368919447 | in-del | -/ATAAGATG | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122896741 | AAGCCACATAAGATG[-/ATAAGATG]GCTGGGTGCAGTGGC | 54542 |
rs368997718 | snp | C/T | 1.65669e-05 | 0.00287805 | missense | RC3H2 | GRCh38.p7 | 9:122858961 | GAATTCATTCGATCT[C/T]GAGGGGAAAATGTAC | 54542 |
rs369000975 | snp | C/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122891782 | AAAGCATTCAACAGG[C/T]ACAAAATACTCAATA | 54542 |
rs369176515 | snp | C/T | 1.66059e-05 | 0.00288144 | synonymous-codon | RC3H2 | GRCh38.p7 | 9:122893003 | ACCTAGATTACTTAA[C/T]TTAATTGACTGATGA | 54542 |
rs369185725 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122867475 | GGGGTCAGCCCCCCG[A/C]CCGGCCAGCCGCCCT | 54542 |
rs369225844 | snp | C/T | 0.000167986 | 0.00916323 | missense | RC3H2 | GRCh38.p7 | 9:122865407 | CATTAGCGCCAACCT[C/T]TCCCACTTTCTTCAC | 54542 |
rs369228436 | snp | A/C | 0.00435393 | 0.0464544 | intron-variant | RC3H2 | GRCh38.p7 | 9:122890210 | ATATCAAGATTTGTA[A/C]ATATAAAGACGGGTT | 54542 |
rs369268524 | snp | A/C | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122878561 | AGACATGAGCCACCG[A/C]GCCCAGCCCCCTGAC | 54542 |
rs369344194 | snp | A/G | | | missense | RC3H2 | GRCh38.p7 | 9:122858871 | CGCCTGCTGTCGTAC[A/G]CAGGAGCATACATTC | 54542 |
rs369367557 | snp | C/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122860450 | TGTCACTCTGTCACC[C/T]GGGCTGGAGTGCACT | 54542 |
rs369435687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122904251 | CAAGGGTTATGAAAA[C/T]ATAAATAAATCACTG | 54542 |
rs369438698 | snp | A/G | 5.00213e-05 | 0.00500081 | intron-variant | RC3H2 | GRCh38.p7 | 9:122854526 | AGAATTAAGAAGAAC[A/G]TTACCTTTCAACATA | 54542 |
rs369444915 | snp | C/T | 0.000165986 | 0.00910854 | missense | RC3H2 | GRCh38.p7 | 9:122851403 | CCCTATCAGGTTTAG[C/T]ATCTGTTGCATCTTC | 54542 |
rs369447782 | snp | A/G | 0.000167986 | 0.00916323 | intron-variant, downstream-variant-500B | RC3H2, SNORD90 | GRCh38.p7 | 9:122879897 | AGCCACCAAGGGCAT[A/G]GGGGTTGGGGGGGAA | 54542 |
rs369501993 | snp | A/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122890736 | GCCTAATTTTTAGCT[A/G]CTTTAGCAGTTTAAC | 54542 |
rs369557113 | snp | C/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122861218 | AATTTCGGCCGGGCA[C/T]GGTGGCTCACACCTG | 54542 |
rs369641250 | snp | C/T | 1.71249e-05 | 0.00292612 | intron-variant | RC3H2 | GRCh38.p7 | 9:122857891 | CTGTTTGACCTATCC[C/T]TGCAACATTAAGTAA | 54542 |
rs369646864 | snp | A/G | 6.69501e-05 | 0.00578537 | intron-variant, synonymous-codon | RC3H2 | GRCh38.p7 | 9:122853888 | CTCAGTAATGGTATA[A/G]CCAAGATGCAGCAGC | 54542 |
rs369650946 | snp | A/G | 3.31241e-05 | 0.00406952 | synonymous-codon | RC3H2 | GRCh38.p7 | 9:122865501 | TGCATTTGAAATTCC[A/G]TTTGTACTTGGAACA | 54542 |
rs369835054 | snp | A/G | 0.000149243 | 0.00863707 | synonymous-codon | RC3H2 | GRCh38.p7 | 9:122890349 | TCGAGCCCTGACAGC[A/G]GCCCATAGATTGGCA | 54542 |
rs369901450 | snp | A/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122892732 | TGAATTCTTAATAAC[A/G]ATATTGGTTATTTTC | 54542 |
rs369901844 | snp | A/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122867205 | GGAGCGTCTCCGCCC[A/G]GCAGCCACCCCGTCC | 54542 |
rs370023096 | snp | C/T | 1.65773e-05 | 0.00287895 | missense | RC3H2 | GRCh38.p7 | 9:122854597 | CTTGAATCAACAGCA[C/T]TGACATAAGGGACAT | 54542 |
rs370063559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122898802 | AAAAGATTTAGTAGC[A/G]AAACGATACTAATTT | 54542 |
rs370067149 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RC3H2 | GRCh38.p7 | 9:122861485 | ACAAGAGCGAAACTC[C/T]GTCTCAAAAAAAAAA | 54542 |
rs370085658 | snp | A/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122903114 | TCTAGAATATTTAAA[A/T]TATAAAGTAATACTT | 54542 |
rs370214706 | snp | C/T | | | intron-variant, downstream-variant-500B | RC3H2 | GRCh38.p7 | 9:122853286 | GAAAACCAGAGACCT[C/T]TGTTCACTTGTTTAT | 54542 |
rs370277433 | snp | A/G | 6.70208e-05 | 0.00578843 | missense | RC3H2 | GRCh38.p7 | 9:122855207 | CTGATGGGCTTAGTC[A/G]CACTTCCTTGGGAAG | 54542 |
rs370280917 | snp | A/C | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122850130 | TACAGGCATGTGCCA[A/C]CACGCCCAGCTATTT | 54542 |
rs370314971 | snp | A/T | 0.000137589 | 0.00829312 | synonymous-codon | RC3H2 | GRCh38.p7 | 9:122859101 | AGGTGGTGGATAGTA[A/T]CCTTGAAAATTGGAA | 54542 |
rs370403027 | snp | C/T | 8.33882e-05 | 0.00645656 | synonymous-codon | RC3H2 | GRCh38.p7 | 9:122849768 | ATTGCTAATAGACAC[C/T]GGGAGTGGCTGGCTA | 54542 |
rs370465353 | snp | G/T | 0.000167986 | 0.00916323 | missense | RC3H2 | GRCh38.p7 | 9:122877507 | TGGGCAAATGTACAA[G/T]TTGTTCCTCGTGGAC | 54542 |
rs370484206 | in-del | -/C | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122866375 | TCTCCCCCTCCCCCT[-/C]CCCCCTCCCTCTCCC | 54542 |
rs370485400 | snp | C/T | 0.00154609 | 0.0277606 | intron-variant, nc-transcript-variant | RC3H2, SNORD90 | GRCh38.p7 | 9:122880214 | TCAACATATTTAATA[C/T]GTTTTCAAGTGTCTT | 54542 |
rs370510263 | snp | A/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122861672 | TTATGCAGGAACTCA[A/G]TACATTGCATCTCAA | 54542 |
rs370547104 | snp | C/T | 1.67837e-05 | 0.00289682 | intron-variant, downstream-variant-500B | RC3H2, SNORD90 | GRCh38.p7 | 9:122880209 | ATTTATCAACATATT[C/T]AATACGTTTTCAAGT | 54542 |
rs370575996 | snp | C/T | 0.000282221 | 0.0118756 | intron-variant | RC3H2 | GRCh38.p7 | 9:122855432 | TCAATAAAAGGACTG[C/T]TGGCAATTACTTCAG | 54542 |
rs370583892 | snp | C/G | 1.75671e-05 | 0.00296366 | intron-variant, nc-transcript-variant | RC3H2, SNORD90 | GRCh38.p7 | 9:122880281 | TTTTCACCTCAGAAT[C/G]TGCCCTATGAAATTC | 54542 |
rs370588985 | snp | C/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122892345 | CTCAAACTCCTGGGC[C/T]CAAGAAATCTACCCA | 54542 |
rs370666034 | snp | A/G | 8.29263e-05 | 0.00643865 | intron-variant | RC3H2 | GRCh38.p7 | 9:122877614 | CACATTCAATGAGTG[A/G]CAAGGTGAAGATTCC | 54542 |
rs370690984 | snp | C/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122866381 | CCTCCCCCTCCCCCC[C/T]CCCTCTCCCCACGGT | 54542 |
rs370767074 | snp | A/G | 4.97467e-05 | 0.00498707 | intron-variant | RC3H2 | GRCh38.p7 | 9:122877609 | GGGAACACATTCAAT[A/G]AGTGGCAAGGTGAAG | 54542 |
rs370804584 | snp | C/G | 1.65641e-05 | 0.00287781 | missense | RC3H2 | GRCh38.p7 | 9:122858047 | CACTGATCTGGCTTT[C/G]TTCTTATCTGCTCCT | 54542 |
rs370988032 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RC3H2 | GRCh38.p7 | 9:122899709 | TCCAGTTTTCTGGTT[C/T]GCAGAGTTATACAAG | 54542 |
rs370991398 | snp | C/T | 0.000165986 | 0.00910854 | intron-variant, upstream-variant-2KB | RC3H2, SNORD90 | GRCh38.p7 | 9:122880578 | ATAGAACATCAGCAT[C/T]TCTAATTTCACAAAC | 54542 |
rs371024220 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RC3H2 | GRCh38.p7 | 9:122894071 | GAGACCATCCTGGCT[A/G]ACACGGTGAAACCCT | 54542 |
rs371101810 | snp | A/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122888025 | GCTGGGATTACAGGC[A/G]TGAGCCACTGCGCCT | 54542 |
rs371202574 | snp | A/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122871625 | ACTGCGCCTGGCCAA[A/G]TGTTGTATCTTCTAA | 54542 |
rs371208316 | snp | C/T | 0.000169986 | 0.00921758 | intron-variant | RC3H2 | GRCh38.p7 | 9:122893062 | AATATTGCAGAAATA[C/T]ATTCATCCAGCTCAT | 54542 |
rs371211546 | snp | A/C/T | 8.6915e-05 | 0.00659166 | missense | RC3H2 | GRCh38.p7 | 9:122859057 | ACAAAGCGAGGAACA[A/C/T]AGGGAGCCACACCAG | 54542 |
rs371214878 | snp | C/T | 4.97286e-05 | 0.00498616 | intron-variant | RC3H2 | GRCh38.p7 | 9:122854090 | GTTGCTCTTGGCCTA[C/T]ATGAGGAGGGAAAAA | 54542 |
rs371367501 | snp | C/G | 1.65625e-05 | 0.00287766 | missense | RC3H2 | GRCh38.p7 | 9:122865387 | GGGCCCAGCAGCATT[C/G]TGACCATTAGCGCCA | 54542 |
rs371429942 | snp | G/T | 1.78334e-05 | 0.00298603 | intron-variant | RC3H2 | GRCh38.p7 | 9:122858635 | CCAGACACTGGGCTG[G/T]TAATGACTACATTAT | 54542 |
rs371434786 | snp | C/T | 0.000413629 | 0.0143751 | intron-variant | RC3H2 | GRCh38.p7 | 9:122897250 | TGATTATTTTTGCAC[C/T]AACCTATAGTAAAAT | 54542 |
rs371462016 | snp | C/T | 3.32823e-05 | 0.00407922 | intron-variant | RC3H2 | GRCh38.p7 | 9:122855721 | CCCCTGCAACCCCAG[C/T]AAAATCATACCATTA | 54542 |
rs371479233 | snp | C/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122875869 | ATGCAGGGTCTTAGA[C/G]GCCACAACATAGATT | 54542 |
rs371486566 | snp | A/G | 0.000182148 | 0.00954153 | missense | RC3H2 | GRCh38.p7 | 9:122858922 | GGTCCATACGGCTGC[A/G]GAGGAGGAGGCTGGT | 54542 |
rs371560616 | snp | C/T | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122868579 | ACCACTCCCTAATCT[C/T]AAGTACCCAGGGACA | 54542 |
rs371619380 | snp | A/G | 0.000167986 | 0.00916323 | intron-variant, downstream-variant-500B | RC3H2, SNORD90 | GRCh38.p7 | 9:122879877 | GTGAAACAGCGTCTA[A/G]AATAAGCCACCAAGG | 54542 |
rs371626611 | snp | A/T | 5.06924e-05 | 0.00503424 | intron-variant | RC3H2 | GRCh38.p7 | 9:122865668 | GATACCTGTTTCAAA[A/T]ACAATCAACAGATTG | 54542 |
rs371657622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122875574 | ACTTCATAAAGAAGT[C/T]TGTCAAGCTCTAAAA | 54542 |
rs371667318 | snp | A/G | 1.66601e-05 | 0.00288614 | missense | RC3H2 | GRCh38.p7 | 9:122855830 | ACCAGGGAGAATAAT[A/G]GGAAAGATGATCTTC | 54542 |
rs371731036 | in-del | -/CT | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122860443 | ACAGGGTGTCACTCT[-/CT]GTCACCCGGGCTGGA | 54542 |
rs371766898 | in-del | -/GTGTGTGTGTGTGTGTATGTG/TTTT | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122868875 | TGTGTGTGTGTGTGT[-/GTGTGTGTGTGTGTGTATGTG/TTTT]TTTTTTTTTTTTTTT | 54542 |
rs371799732 | in-del | AT/G | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122856814 | AACTTTTCTCAAGTC[AT/G]AACTCAGCAGATCGG | 54542 |
rs371825609 | snp | A/C | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122890172 | CAATAACAACAACAA[A/C]AAAAACAAATTTATC | 54542 |
rs371827475 | snp | C/T | 1.78953e-05 | 0.00299121 | intron-variant, upstream-variant-2KB | RC3H2, SNORD90 | GRCh38.p7 | 9:122880819 | AGAAAAGAGAAAAAT[C/T]AGAATTGGTCTGTGC | 54542 |
rs371832955 | snp | C/T | 1.65682e-05 | 0.00287817 | intron-variant | RC3H2 | GRCh38.p7 | 9:122851316 | ATTATCTAATTGTGG[C/T]ACTTACTTCAATTGG | 54542 |
rs371837514 | snp | A/G/T | 3.31253e-05 | 0.00406962 | missense | RC3H2 | GRCh38.p7 | 9:122851153 | TGCTGCTGTACTGGA[A/G/T]GCCCATTTTCCACTG | 54542 |
rs371884585 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RC3H2 | GRCh38.p7 | 9:122868987 | GCTCACTGCAACCTC[C/T]GCCTCCTGGGTTCAA | 54542 |
rs371930038 | snp | C/T | 3.31461e-05 | 0.00407086 | synonymous-codon | RC3H2 | GRCh38.p7 | 9:122858720 | TGGCTGACAAGCCAC[C/T]GAATAATATCCATCT | 54542 |
rs371943827 | snp | C/T | 0.000165986 | 0.00910855 | utr-variant-5-prime | RC3H2 | GRCh38.p7 | 9:122897510 | TGCCTGCACAGGCAT[C/T]GTGGAAGCTGGATGC | 54542 |
rs371955901 | snp | A/G | 1.70107e-05 | 0.00291634 | intron-variant | RC3H2 | GRCh38.p7 | 9:122854499 | TACAAGTCTGAGAAT[A/G]GAGAATCATATAGAA | 54542 |
rs372023688 | snp | C/T | 6.62394e-05 | 0.00575459 | missense | RC3H2 | GRCh38.p7 | 9:122858839 | CATCTCGTTGGTACA[C/T]AGGTGGGCGCCAGAT | 54542 |
rs372046057 | snp | A/C | | | intron-variant | RC3H2 | GRCh38.p7 | 9:122866812 | CTGAGATTGCAGCCT[A/C]TGCCCGGCCGCCACC | 54542 |
rs372048548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RC3H2 | GRCh38.p7 | 9:122863424 | ATATAAGCCTTCAGA[C/T]CTAAAAGACTGGTCT | 54542 |
rs372086743 | snp | C/T | | | missense | RC3H2 | GRCh38.p7 | 9:122858868 | ATGCGCCTGCTGTCG[C/T]ACACAGGAGCATACA | 54542 |
rs372131836 | snp | A/C/T | 1.68001e-05 | 0.00289823 | intron-variant | RC3H2 | GRCh38.p7 | 9:122860181 | ATCACTGTCTATGAC[A/C/T]GTCCTCCTTACTAGA | 54542 |
rs372146850 | snp | A/T | 3.45012e-05 | 0.00415324 | intron-variant | RC3H2 | GRCh38.p7 | 9:122857872 | ATGAGTAATTTGAAG[A/T]CAGCTGTTTGACCTA | 54542 |
rs372151949 | snp | C/T | 0.000167986 | 0.00916324 | missense | RC3H2 | GRCh38.p7 | 9:122883377 | AGGCCTCTTCTTGCA[C/T]AGCTAAAAATATTAA | 54542 |