SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs335675 | snp | C/T | 0.170084 | 0.236883 | intron-variant | FBXO22 | GRCh38.p7 | 15:75927944 | TTCCTGTCCCCAAAG[C/T]ACCCGTTTGGTAATG | 26263 |
rs335676 | snp | C/T | 0.13446 | 0.221699 | intron-variant | FBXO22 | GRCh38.p7 | 15:75928171 | gtaaattagttcagc[C/T]attgtggaagatagt | 26263 |
rs335677 | snp | C/G | 0.0777841 | 0.181223 | intron-variant | FBXO22 | GRCh38.p7 | 15:75929247 | GGATTTAGAGCCCAC[C/G]TGGATAGACCAGATG | 26263 |
rs335678 | snp | A/G | 0.0948562 | 0.196037 | intron-variant | FBXO22 | GRCh38.p7 | 15:75929595 | GTACATAGCTGCTTC[A/G]TTATTTGTGTTGATT | 26263 |
rs335679 | snp | G/T | 0.17138 | 0.237316 | intron-variant | FBXO22 | GRCh38.p7 | 15:75929799 | TAAGGTGGAGTGCAA[G/T]TCAGTAACATTTCAT | 26263 |
rs335680 | snp | C/G | 0.029116 | 0.117091 | utr-variant-3-prime, intron-variant | FBXO22 | GRCh38.p7 | 15:75930494 | TGACAGTTCCCAAAT[C/G]TGTTTGGTCACAAAA | 26263 |
rs335681 | snp | A/G | 0.329317 | 0.237084 | downstream-variant-500B, intron-variant | FBXO22 | GRCh38.p7 | 15:75930927 | CTTCTGGTTATCTCT[A/G]TGAGCTAGATCTGGG | 26263 |
rs335682 | snp | C/T | 0.029116 | 0.117091 | upstream-variant-2KB | FBXO22 | GRCh38.p7 | 15:75902408 | cccagccAGTTtttt[C/T]ccatagtctatttat | 26263 |
rs335683 | snp | C/T | 0.172028 | 0.23753 | upstream-variant-2KB | FBXO22 | GRCh38.p7 | 15:75902145 | cgttcatacctcccc[C/T]gcccctcagctaact | 26263 |
rs335684 | snp | A/G | 0.172028 | 0.23753 | upstream-variant-2KB | FBXO22 | GRCh38.p7 | 15:75901963 | cagtttaccagtgac[A/G]GCATCACtacatttt | 26263 |
rs335685 | snp | C/G | 0.474992 | 0.108989 | upstream-variant-2KB | FBXO22 | GRCh38.p7 | 15:75901945 | ATCACTACATTTTTG[C/G]AAATATTTAATTTGT | 26263 |
rs335693 | snp | A/G | 0.133777 | 0.221342 | intron-variant | FBXO22 | GRCh38.p7 | 15:75921583 | acctctgcctcccag[A/G]ttcaagcgattctcc | 26263 |
rs335694 | snp | A/G | 0.169435 | 0.236663 | intron-variant | FBXO22 | GRCh38.p7 | 15:75921023 | ggctgtaacatctag[A/G]tctgtgtaagtacta | 26263 |
rs335695 | snp | A/G | 0.133435 | 0.221162 | intron-variant | FBXO22 | GRCh38.p7 | 15:75920786 | acccaggctgcagta[A/G]agtggcgtgacttca | 26263 |
rs335696 | snp | C/T | 0.029116 | 0.117091 | intron-variant | FBXO22 | GRCh38.p7 | 15:75919703 | GGCCCATGTGACACA[C/T]AGTAAAGCCTGCCTA | 26263 |
rs335697 | snp | A/G | 0.323671 | 0.238899 | intron-variant | FBXO22 | GRCh38.p7 | 15:75918026 | TTCCTTGAGTAATTC[A/G]TTTGTTGTTTACTAT | 26263 |
rs335698 | snp | A/C | 0.039522 | 0.134904 | intron-variant | FBXO22 | GRCh38.p7 | 15:75917795 | AGAACTAACCCGCGT[A/C]TTCTAAAAACTTCTA | 26263 |
rs335699 | snp | A/G | 0.021333 | 0.101051 | intron-variant | FBXO22 | GRCh38.p7 | 15:75916954 | GGTATTTATCATGCT[A/G]TTCTATTATTCTTTC | 26263 |
rs335700 | snp | C/T | 0.135484 | 0.22223 | intron-variant | FBXO22 | GRCh38.p7 | 15:75916568 | tttaagccctaaccc[C/T]ccatgtgactatatt | 26263 |
rs335701 | snp | C/T | 0.0980852 | 0.198549 | intron-variant | FBXO22 | GRCh38.p7 | 15:75915024 | GTAGAGATCACGCCA[C/T]TGCACTCCAACCTTG | 26263 |
rs335702 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | FBXO22 | GRCh38.p7 | 15:75911748 | gagaaagaataaagc[A/G]tattcaaataggaag | 26263 |
rs335703 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | FBXO22 | GRCh38.p7 | 15:75911377 | aggataggaagaatc[A/G]atatcgtgaaaatgc | 26263 |
rs335704 | snp | A/T | 0.0379877 | 0.132479 | intron-variant | FBXO22 | GRCh38.p7 | 15:75909789 | tgtatcgcagaaatt[A/T]aaAAAAAAAAAAAAG | 26263 |
rs335705 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | FBXO22 | GRCh38.p7 | 15:75908913 | AAGAGACAGATAGCA[C/T]GATGGCCTGTGGggc | 26263 |
rs335706 | snp | A/G | 0.325327 | 0.238382 | intron-variant | FBXO22 | GRCh38.p7 | 15:75908490 | CTGAGGCCAGGGTGA[A/G]ACCAGCCTGTCCAAC | 26263 |
rs335707 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | FBXO22 | GRCh38.p7 | 15:75908421 | ACCGGGTATGGCTGC[A/G]TGCGCCTGTAGTCCC | 26263 |
rs335724 | snp | A/C | 0.0962929 | 0.197165 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | FBXO22, FBXO22-AS1 | GRCh38.p7 | 15:75934664 | TGAAAAGTTTTGACA[A/C]ATTTTTCTTTGGACT | 26263 |
rs974718 | snp | A/G | 0.0970103 | 0.197722 | upstream-variant-2KB | FBXO22 | GRCh38.p7 | 15:75903623 | GTGGCGGGAGCTTGT[A/G]GTTAAAGCTACGAGG | 26263 |
rs1394122 | snp | C/T | 0.16976 | 0.236773 | intron-variant | FBXO22 | GRCh38.p7 | 15:75925270 | TGTAACAACCTGTTA[C/T]GTATTGTTTTATTCC | 26263 |
rs1617498 | snp | A/G | 0.029116 | 0.117091 | intron-variant | FBXO22 | GRCh38.p7 | 15:75924041 | aaggtgcgggttgga[A/G]gatcagattatcagt | 26263 |
rs1695372 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | FBXO22 | GRCh38.p7 | 15:75924757 | ATCTTGCCAACGCTC[A/G]GCAGTGCTAGGTCTG | 26263 |
rs1695379 | snp | A/C | 0.00453512 | 0.0474025 | utr-variant-3-prime, nc-transcript-variant | FBXO22, NRG4 | GRCh38.p7 | 15:75935263 | GGAGTATTAGCTAAA[A/C]ACAAACTAAATTCCT | 26263 |
rs1699263 | snp | A/G | 0.326506 | 0.238006 | intron-variant | FBXO22 | GRCh38.p7 | 15:75906367 | TTAGAGCCAAGGAAT[A/G]TAAGTATGTATATAC | 26263 |
rs1699264 | snp | A/T | 0 | 0 | intron-variant | FBXO22 | GRCh38.p7 | 15:75906791 | TATCATTTGGAAAAA[A/T]TCAAAATGCAAGCAG | 26263 |
rs2201917 | snp | A/G | 0.499997 | 0.00119808 | intron-variant | FBXO22 | GRCh38.p7 | 15:75912174 | cctcaataaaatact[A/G]gcagaccgaatccag | 26263 |
rs2255701 | snp | A/G | 0.324619 | 0.238604 | intron-variant | FBXO22 | GRCh38.p7 | 15:75904368 | TCCAAAGTCCCCGGG[A/G]TAGGTAGGTGTCAGT | 26263 |
rs2455893 | snp | A/C | 0.039522 | 0.134904 | intron-variant | FBXO22 | GRCh38.p7 | 15:75915431 | GCCCTTTAGAAACCA[A/C]AGCTAGAGCAACTGA | 26263 |
rs2455895 | snp | A/G | 0.039522 | 0.134904 | intron-variant | FBXO22 | GRCh38.p7 | 15:75904333 | GCGCTAGTTCGGAAG[A/G]AGAGCCAGATATGGA | 26263 |
rs2460811 | snp | A/G | 0 | 0 | intron-variant | FBXO22 | GRCh38.p7 | 15:75926212 | ATGGCGGGTGGCCCA[A/G]AACATTGGGTCCTTG | 26263 |
rs2648435 | snp | G/T | 0.134119 | 0.221521 | intron-variant | FBXO22 | GRCh38.p7 | 15:75927424 | TTTAGAAGTCATGAG[G/T]TTTCTAAAAGCTAAA | 26263 |
rs2648436 | snp | A/C | 0.0295035 | 0.117819 | intron-variant | FBXO22 | GRCh38.p7 | 15:75926073 | TAAACAGTGTAACCT[A/C]CTGGTGAACCTTTCA | 26263 |
rs2655134 | snp | C/T | 0 | 0 | intron-variant | FBXO22 | GRCh38.p7 | 15:75916004 | gaagtggtgcaacct[C/T]tgcctcccggtttcc | 26263 |
rs2655135 | snp | A/G | 0.021333 | 0.101051 | intron-variant | FBXO22 | GRCh38.p7 | 15:75915963 | ctgcctcagcctccc[A/G]agtagctggaattac | 26263 |
rs3073843 | in-del | -/AGA | 0.030278 | 0.119257 | intron-variant | FBXO22 | GRCh38.p7 | 15:75904730 | TTTCACGGAACGAGA[-/AGA]TGTTCCTTTAATTAA | 26263 |
rs3833815 | in-del | -/A | 0.00358779 | 0.0422022 | utr-variant-3-prime, intron-variant | FBXO22 | GRCh38.p7 | 15:75930265 | AATGTGACTCAAGGA[-/A]GTTCTTGAAGGACAA | 26263 |
rs3991408 | in-del | -/A/AA/AAA | 0.469247 | 0.120128 | intron-variant | FBXO22 | GRCh38.p7 | 15:75904826 | aaaaaanaaaaaaaa[-/A/AA/AAA]NGGCCCAACATTTGA | 26263 |
rs4278711 | snp | C/G | 0 | 0 | intron-variant | FBXO22 | GRCh38.p7 | 15:75928434 | cacgtcctttgcagg[C/G]acatggatggagctg | 26263 |
rs4886466 | snp | A/G | 0.49681 | 0.0398085 | intron-variant | FBXO22 | GRCh38.p7 | 15:75907963 | AAAAAAAATTTTTTT[A/G]AAGTCCACCAAAAGC | 26263 |
rs4886750 | snp | C/T | 0.0980852 | 0.198549 | intron-variant | FBXO22 | GRCh38.p7 | 15:75915712 | caagagcagcctggc[C/T]gacgtggtgaaaccc | 26263 |
rs7177266 | snp | C/T | 0.496483 | 0.0417852 | upstream-variant-2KB | FBXO22 | GRCh38.p7 | 15:75903599 | AAATACAAAAATTAG[C/T]TGGGCGTGGTGGCGG | 26263 |
rs8038182 | snp | A/C | 0 | 0 | intron-variant | FBXO22 | GRCh38.p7 | 15:75919894 | ACTGTGCTGCGCAGC[A/C]CTTCTAATCTTCACC | 26263 |
rs10152926 | snp | A/T | 0.0418186 | 0.138422 | intron-variant | FBXO22 | GRCh38.p7 | 15:75924114 | tatagacagttggat[A/T]tgttggcctggagct | 26263 |
rs10163130 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant, downstream-variant-500B | FBXO22, FBXO22-AS1 | GRCh38.p7 | 15:75932602 | AGGCAGCAGCCTCCC[A/G]TCAGTGAATCAGGAG | 26263 |
rs10468061 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | FBXO22 | GRCh38.p7 | 15:75915460 | GCTTAACATTTTTTT[A/T]AAAAAAAGAGTTTAT | 26263 |
rs10468062 | snp | A/G | 0.0980852 | 0.198549 | intron-variant | FBXO22 | GRCh38.p7 | 15:75915467 | ATTTTTTTAAAAAAA[A/G]GAGTTTATTTCTTTT | 26263 |
rs10591372 | in-del | -/AAA | 0 | 0 | intron-variant | FBXO22 | GRCh38.p7 | 15:75916077 | AAAAAAAAAAAAAAA[-/AAA]GTTTATTTCTTTTTT | 26263 |
rs11072563 | snp | A/G | 0.214541 | 0.247473 | intron-variant | FBXO22 | GRCh38.p7 | 15:75928332 | ctattcacagtagca[A/G]agacatggaatcaac | 26263 |
rs11378024 | in-del | -/A | 0.192715 | 0.243348 | intron-variant | FBXO22 | GRCh38.p7 | 15:75929309 | CCAAAAAAAAAAAAA[-/A]TTTTTTTTAAAGATC | 26263 |
rs11636664 | snp | C/T | 0 | 0 | upstream-variant-2KB | FBXO22 | GRCh38.p7 | 15:75902836 | TTTCTGCCCAAGATC[C/T]GGCGATCAAATCAGG | 26263 |
rs12437816 | snp | C/G | 0.49645 | 0.0419827 | upstream-variant-2KB | FBXO22 | GRCh38.p7 | 15:75902197 | agacaagcaggcata[C/G]tccctgaacatgctg | 26263 |
rs12440944 | snp | A/C | | | intron-variant | FBXO22 | GRCh38.p7 | 15:75911137 | tatatctgttttggt[A/C]ccagtaccatgctgt | 26263 |
rs12441092 | snp | C/G | 0.00755907 | 0.0610114 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | FBXO22, FBXO22-AS1 | GRCh38.p7 | 15:75934008 | GATGTgcagagagca[C/G]caattttccttcaat | 26263 |
rs12910038 | snp | A/C | 0.300169 | 0.244914 | intron-variant | FBXO22 | GRCh38.p7 | 15:75931784 | CAGGCAAATATAAAC[A/C]AAAACAAAGCATGAG | 26263 |
rs12912046 | snp | A/T | | | intron-variant | FBXO22 | GRCh38.p7 | 15:75912926 | aatttccctgtaaac[A/T]ctgctttagctgtgt | 26263 |
rs12912173 | snp | C/T | | | intron-variant | FBXO22 | GRCh38.p7 | 15:75912879 | caattttagatcttt[C/T]ctgctttctcctgtg | 26263 |
rs12913306 | snp | G/T | | | intron-variant | FBXO22 | GRCh38.p7 | 15:75912895 | ctgctttctcctgtg[G/T]gcatttagtgctata | 26263 |
rs16967642 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | FBXO22 | GRCh38.p7 | 15:75913467 | CCTTTCTGCTTCAGA[C/T]TGATTTCTAAACCTT | 26263 |
rs16967653 | snp | C/T | 0.0256043 | 0.110214 | intron-variant | FBXO22 | GRCh38.p7 | 15:75917226 | TGTTTAACTTTTTCT[C/T]TAGTGACTCCAATGG | 26263 |
rs17427842 | snp | C/T | 0.300169 | 0.244914 | intron-variant | FBXO22 | GRCh38.p7 | 15:75927820 | CATCTGCATACCCTT[C/T]GTTTCCTTAAGTAAC | 26263 |
rs17428029 | snp | C/T | 0.0205511 | 0.0992634 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | FBXO22, FBXO22-AS1 | GRCh38.p7 | 15:75933379 | AGCTGCTGTGTAACA[C/T]GACCTTAAATAGTCT | 26263 |
rs28411993 | snp | C/T | | | intron-variant | FBXO22 | GRCh38.p7 | 15:75920080 | GAAAAGGTCAGATAG[C/T]GCCCTTAAAACTGAC | 26263 |
rs28579689 | snp | A/C | 0.0729998 | 0.176553 | downstream-variant-500B, utr-variant-3-prime | FBXO22, NRG4 | GRCh38.p7 | 15:75935510 | AAGGCTTAAGCAAGG[A/C]ATATATTTCCATGCC | 26263 |
rs28636006 | snp | C/T | 0.0633504 | 0.166319 | intron-variant | FBXO22 | GRCh38.p7 | 15:75917083 | TTAAATGGCAAACAT[C/T]ATGACACTACACCCT | 26263 |
rs34255722 | snp | A/G | 0.00164595 | 0.0286403 | synonymous-codon, nc-transcript-variant | FBXO22, FBXO22-AS1 | GRCh38.p7 | 15:75932958 | TCCATTTCCAAAGAA[A/G]CCGAATAAGGGAACA | 26263 |
rs34335689 | in-del | -/G | | | intron-variant | FBXO22 | GRCh38.p7 | 15:75926465 | CTTTAAGTTGGGGTA[-/G]GGGGAAAGTGATTCT | 26263 |
rs34433647 | in-del | -/G | | | intron-variant | FBXO22 | GRCh38.p7 | 15:75926178 | AAAATTCTAGAATAA[-/G]AATCTGTAGTCAGAT | 26263 |
rs34494278 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FBXO22 | GRCh38.p7 | 15:75913866 | TTTGACATCACTGGG[A/G]CAAAAGCAATATATG | 26263 |
rs34838406 | in-del | -/T | | | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant, downstream-variant-500B | FBXO22, FBXO22-AS1, NRG4 | GRCh38.p7 | 15:75935009 | TTATAGCTGAGCCTT[-/T]GGAGCTTGTTATGAA | 26263 |
rs34907942 | in-del | -/G | | | intron-variant | FBXO22 | GRCh38.p7 | 15:75926113 | TAAATACTTTTCTGG[-/G]AATTGTTTTTAATGG | 26263 |
rs35005442 | in-del | -/A | | | upstream-variant-2KB | FBXO22 | GRCh38.p7 | 15:75902926 | GCTGTGCTTCCATTT[-/A]CTTGGTGGTTCTCAG | 26263 |
rs35111597 | in-del | -/C | | | intron-variant | FBXO22 | GRCh38.p7 | 15:75913757 | TGTCTAATTTGATCC[-/C]AGGTGACTGTTGATG | 26263 |
rs35139316 | in-del | -/T | 0.375 | 0.216506 | intron-variant | FBXO22 | GRCh38.p7 | 15:75929515 | TGTTTTTTTTTTTTT[-/T]GTTCCCTACTGAGAG | 26263 |
rs35315141 | in-del | -/A | | | downstream-variant-500B, utr-variant-3-prime | FBXO22, NRG4 | GRCh38.p7 | 15:75935466 | ACTTTCAAAGCAAAA[-/A]TAATTTCTGGGGCTA | 26263 |
rs35364874 | snp | A/T | 0.364193 | 0.222396 | intron-variant | FBXO22 | GRCh38.p7 | 15:75929323 | CCAAAAAAAAAAAAA[A/T]TTTTTTTAAAGATCC | 26263 |
rs35459926 | in-del | -/G | | | intron-variant | FBXO22 | GRCh38.p7 | 15:75918215 | ACTTAAACCAGCTGG[-/G]AGTAAAAAATTGTGT | 26263 |
rs35659477 | snp | A/G | 0.000832505 | 0.0203853 | missense, nc-transcript-variant | FBXO22, FBXO22-AS1 | GRCh38.p7 | 15:75932699 | ACACCCGAGGCATCA[A/G]TATCCAGAGGGTTCC | 26263 |
rs35775467 | in-del | -/C | | | intron-variant | FBXO22 | GRCh38.p7 | 15:75919820 | GAGCATACATGTGTC[-/C]TGGGCTTGAAGTGAC | 26263 |
rs35865885 | in-del | -/T | | | intron-variant | FBXO22 | GRCh38.p7 | 15:75924096 | GAGATGGAGATATTG[-/T]ATTATAGACAGTTGG | 26263 |
rs36061952 | in-del | -/T | | | intron-variant | FBXO22 | GRCh38.p7 | 15:75924111 | ATTATAGACAGTTGG[-/T]ATATGTTGGCCTGGA | 26263 |
rs36117562 | in-del | -/G | | | intron-variant | FBXO22 | GRCh38.p7 | 15:75921571 | AGGCTGAGGCAGGAG[-/G]AATCGCTTGAATCTG | 26263 |
rs55719276 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | FBXO22 | GRCh38.p7 | 15:75925865 | GAAAAATTCCTAAGA[A/G]GATGGGGCAATTCTT | 26263 |
rs55737257 | in-del | -/TCT | 0.53125 | 0.20492 | intron-variant | FBXO22 | GRCh38.p7 | 15:75904733 | ATTAAAGGAACATCT[-/TCT]CGTTCCGTGAAAAGA | 26263 |
rs55782145 | snp | A/C | 0.0611083 | 0.163768 | intron-variant | FBXO22 | GRCh38.p7 | 15:75923813 | ACTGTTGTAGTGGTT[A/C]AGGAAAGAGGAGATG | 26263 |
rs55828994 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | FBXO22 | GRCh38.p7 | 15:75924001 | GCAGCTGTATAGTAC[C/T]ATTGACTAAGGTGAA | 26263 |
rs56311307 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | FBXO22 | GRCh38.p7 | 15:75929798 | TTAAGGTGGAGTGCA[A/G]GTCAGTAACATTTCA | 26263 |
rs56676669 | snp | G/T | | | intron-variant | FBXO22 | GRCh38.p7 | 15:75904174 | CCCAGGCTGGCGGGG[G/T]GGGGGGAGAGACCCT | 26263 |
rs56709997 | in-del | -/AA | | | intron-variant | FBXO22 | GRCh38.p7 | 15:75928740 | AACTTAAAAAAAAAA[-/AA]TCAAATTGATAGTCT | 26263 |
rs57011816 | snp | A/C | 0.0611083 | 0.163768 | intron-variant | FBXO22 | GRCh38.p7 | 15:75926554 | CTAGAGAAGATGTTG[A/C]AAGAACACCACTGGA | 26263 |
rs57562463 | snp | A/G | 0.0119091 | 0.0762411 | downstream-variant-500B, intron-variant | FBXO22 | GRCh38.p7 | 15:75931005 | AGGAAGGCCAAGTAC[A/G]TTGAATCCCAGGCAG | 26263 |
rs58314879 | in-del | -/T/TT | 0 | 0 | intron-variant | FBXO22 | GRCh38.p7 | 15:75904841 | TTTTTTTTTTTTTTT[-/T/TT]GAGACGTAGTCTCGC | 26263 |