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 |