SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs2053 | snp | C/T | 0.448066 | 0.152544 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22499475 | ATCTCTTTAAAATGC[C/T]TTTTCACTGACAGCA | 9923 |
rs104861 | snp | C/G | 0.475965 | 0.106957 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22518458 | GAGGGTTGCTCTTGT[C/G]ACCaataataacagt | 9923 |
rs169711 | snp | A/T | 0 | 0 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22522769 | AGATATACCAttttt[A/T]ttttttttttttttg | 9923 |
rs182355 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant, utr-variant-5-prime | ZBTB40 | GRCh38.p7 | 1:22509540 | tttagtggagacggg[A/G]tttcgccatgttggc | 9923 |
rs209719 | snp | A/G | 0.337841 | 0.23406 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22521059 | CCAGGGAGCTGGGGC[A/G]CAGCCGAGCAAGCTG | 9923 |
rs209720 | snp | C/T | 0.00594802 | 0.0542092 | missense, nc-transcript-variant | ZBTB40 | GRCh38.p7 | 1:22520216 | CAACGTGGGTCACCA[C/T]GTGCCGCTCCAGCAT | 9923 |
rs209721 | snp | C/T | 0.101658 | 0.201233 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22517067 | ACAAAGGAATAAGGA[C/T]GGAGTTCTCACTGCA | 9923 |
rs209722 | snp | C/T | 0.499663 | 0.0129749 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22516935 | TCCCCTGGCGACATA[C/T]ACAGTGTGGATCTGC | 9923 |
rs209723 | snp | A/G | 0.499653 | 0.0131743 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22514574 | gtgaggaagtgaaac[A/G]tgAGATGTCTGATGG | 9923 |
rs209724 | snp | A/G | 0.499653 | 0.0131743 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22513968 | CACTGTCTGATCCAC[A/G]GTAGGTGCTTAGTCA | 9923 |
rs209725 | snp | A/C | 0.499642 | 0.0133738 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22513579 | CGAGTAGCTGAGACT[A/C]CAGGTGCCCGCCACC | 9923 |
rs209726 | snp | C/G | 0.292266 | 0.246401 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22513532 | TTGTATTTTTTAGTA[C/G]AGATGGGGTTTCACC | 9923 |
rs209727 | snp | A/G | 0.485418 | 0.084132 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22511356 | CTTCCCACCTGGCCC[A/G]TTCCTTACCAATGTA | 9923 |
rs209728 | snp | A/G | 0.0228947 | 0.104514 | intron-variant, utr-variant-5-prime | ZBTB40 | GRCh38.p7 | 1:22509605 | TCCCAGCACTCTGGC[A/G]AAGCTGAGATGGGTG | 9923 |
rs209729 | snp | C/T | 0.359812 | 0.224591 | missense, utr-variant-5-prime, nc-transcript-variant | ZBTB40 | GRCh38.p7 | 1:22509184 | GAGGTAAAGAGCTTG[C/T]ACTCAATCTTCTGTT | 9923 |
rs209730 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22508880 | TAAAAGGTTTACAAA[C/T]TCTTGTGTCCTTGAA | 9923 |
rs209731 | snp | C/T | 0.0581099 | 0.160244 | intron-variant, upstream-variant-2KB | ZBTB40 | GRCh38.p7 | 1:22507308 | tgaatgcccatgtgc[C/T]gggcacagtgctaaa | 9923 |
rs209732 | snp | A/T | 0.425545 | 0.178 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22506250 | ACCACAGGTATTAGT[A/T]AATTGTTGACTCTCT | 9923 |
rs209752 | snp | A/G | 0.0155062 | 0.0866757 | synonymous-codon, intron-variant, nc-transcript-variant | ZBTB40 | GRCh38.p7 | 1:22501551 | TTCCTCTCTTACTTT[A/G]CCCAGGATTCTCTGG | 9923 |
rs209753 | snp | C/T | 0.441568 | 0.160629 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22495475 | CAGACTCATACTTTT[C/T]TTCAGTTTTTGTGCT | 9923 |
rs209754 | snp | A/G | 0.0599851 | 0.162463 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22490888 | aaaacaaaacaaaac[A/G]aaacaGATAATTATC | 9923 |
rs484885 | snp | A/G | 0.490782 | 0.0672626 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22523262 | aatagttccttaaaa[A/G]tggtacatcttggct | 9923 |
rs485052 | snp | C/T | 0.314544 | 0.241524 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22523203 | agcactttgggaggg[C/T]gaggcgggcggatca | 9923 |
rs489708 | snp | A/G | 0 | 0 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22522711 | TTAACTGGCACTTTA[A/G]ATTTGATGAGTATAG | 9923 |
rs491604 | snp | A/G | | | intron-variant | ZBTB40 | GRCh38.p7 | 1:22522488 | cccgagtctagccta[A/G]aagtATGCTGACAGG | 9923 |
rs717198 | snp | A/G | 0 | 0 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22497790 | aagtaacttgcttaa[A/G]gtcacaggtctagta | 9923 |
rs717200 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22497501 | CTTAGGCTTAATCAT[C/T]AACAGAAAGGAGATT | 9923 |
rs717201 | snp | A/C | | | intron-variant | ZBTB40 | GRCh38.p7 | 1:22497851 | TTCCTCACACCAGGC[A/C]TGGGAGGCGTTACTA | 9923 |
rs761397 | snp | C/T | 0.00795532 | 0.062565 | utr-variant-3-prime, nc-transcript-variant, intron-variant | ZBTB40 | GRCh38.p7 | 1:22526760 | CCCACTGAGCGCTGT[C/T]GGCACATCATGCCTC | 9923 |
rs881646 | snp | C/G | 0.450214 | 0.149733 | synonymous-codon, nc-transcript-variant | ZBTB40 | GRCh38.p7 | 1:22526222 | CCAAACCCCAGAGCC[C/G]GTGGCCCCGACAGAG | 9923 |
rs962889 | snp | A/G | 0.110872 | 0.20771 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | ZBTB40 | GRCh38.p7 | 1:22530759 | TTTGGTTCTGGGCCA[A/G]TGTCAGACGGGGACA | 9923 |
rs963970 | snp | C/G | 0.320335 | 0.239902 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22474966 | TCCAGCTTAATGCAA[C/G]CTTACCTGTTTTTTT | 9923 |
rs998978 | snp | A/C | 0.450462 | 0.149381 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22522510 | AGACTCGGGGCCTGA[A/C]TCTCCCCTCCACCAC | 9923 |
rs1001547 | snp | A/G | 0 | 0 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22469779 | gaggccaaggcaggc[A/G]gtcatttaaggtcag | 9923 |
rs1009444 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22521838 | CAGCTTGAGTGGCAG[C/T]GGTTCTCAAACCTGG | 9923 |
rs1011380 | snp | C/T | 0.321769 | 0.239477 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22479788 | ctgcttataaggtag[C/T]agttaaaaagaaaat | 9923 |
rs1062663 | snp | C/T | 0.441841 | 0.160303 | utr-variant-3-prime, nc-transcript-variant | ZBTB40 | GRCh38.p7 | 1:22530108 | AGTGCTAACCATGTA[C/T]AGAGTGGGCAGGCGG | 9923 |
rs1266996 | snp | A/G | | | intron-variant | ZBTB40 | GRCh38.p7 | 1:22483053 | cctgctctgtcgccc[A/G]ggctggagtagtggc | 9923 |
rs1266997 | snp | C/T | 0.322007 | 0.239405 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22482845 | gtgatccacctgcct[C/T]ggcctcccaaagtgc | 9923 |
rs1266998 | snp | C/T | | | intron-variant | ZBTB40 | GRCh38.p7 | 1:22477578 | cactgcaacctccgc[C/T]tcccgggttcaagca | 9923 |
rs1266999 | snp | C/T | 0.411578 | 0.190768 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22477102 | TAGTGATTTGGGGGC[C/T]ATGGAAATACACTAT | 9923 |
rs1267000 | snp | C/G | 0.339882 | 0.233284 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22476235 | CTGTCTCAAAAGAAA[C/G]TTTGAGGATCCTCTA | 9923 |
rs1267001 | snp | C/T | 0.320575 | 0.239832 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22475579 | GGTAATTTCAAGGTT[C/T]AATTTCAACAGACAA | 9923 |
rs1267003 | snp | A/C/T | 0.0733688 | 0.176922 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22474960 | TTAATGCAACCTTAC[A/C/T]TGTTTTTTTTTTTTT | 9923 |
rs1267004 | snp | A/G | 0 | 0 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22523057 | gggaggctgaggcag[A/G]agaatggcgtgaacc | 9923 |
rs1267005 | snp | A/G | 0.320814 | 0.239761 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22489769 | ATTCATCCAACAAAT[A/G]TTGCTTAATAGGAAG | 9923 |
rs1267006 | snp | A/T | 0.32153 | 0.239548 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22502930 | GTCATCTCTGAGTGG[A/T]GAAATCTGAATTTTT | 9923 |
rs1268659 | snp | A/G | 0.0584853 | 0.160693 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22482860 | cgatctcctgacctc[A/G]tgatccacctgcctt | 9923 |
rs1268660 | snp | C/T | | | intron-variant | ZBTB40 | GRCh38.p7 | 1:22477529 | cctgagtagctggga[C/T]tacaggcgcctgcca | 9923 |
rs1268661 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22472984 | ACAATGTCCAAAGTA[C/T]CTCTGGGAATAAATC | 9923 |
rs1271035 | snp | C/T | | | intron-variant | ZBTB40 | GRCh38.p7 | 1:22477490 | agctaatttttgtat[C/T]tttagtagagacggg | 9923 |
rs1272162 | snp | A/C | | | intron-variant | ZBTB40 | GRCh38.p7 | 1:22477454 | accacgttggccagg[A/C]tggtctcgaactcct | 9923 |
rs1272408 | snp | A/G | | | intron-variant | ZBTB40 | GRCh38.p7 | 1:22523035 | gcgtgaacctgggag[A/G]cggagcttgcagtga | 9923 |
rs1320602 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22454992 | CCCTCTTTCTGGAGA[C/T]AGAAAGTAGAGGGCT | 9923 |
rs1344194 | snp | A/G | 0.494651 | 0.0514399 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22463248 | GTGATGCCAGCGGCT[A/G]TGTGCTCTACAGTAA | 9923 |
rs1738392 | snp | A/G | 0.322007 | 0.239405 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22487407 | GTTTGAGGAAATTAT[A/G]TAATCTCACTTGTAA | 9923 |
rs1769819 | snp | C/T | 0.441432 | 0.160792 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22483328 | aaggaatgtgattac[C/T]agatcatgtggcaag | 9923 |
rs1769820 | snp | A/T | 0.44858 | 0.151875 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22485030 | attctctttaggcat[A/T]gttagagtcaagttg | 9923 |
rs1769821 | snp | A/G | 0.322245 | 0.239334 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22486713 | ggcgtttgttcatac[A/G]ttttttttgttttgt | 9923 |
rs1769822 | snp | C/T | | | intron-variant | ZBTB40 | GRCh38.p7 | 1:22523010 | tggagtgcagtggcg[C/T]gatctcggctcactg | 9923 |
rs1890775 | snp | A/G | 0.495521 | 0.0471118 | | | GRCh38.p7 | 1:22447773 | CCAAATGACTCAGAA[A/G]GGTCAACTGCCTGCC | 9923 |
rs1934482 | snp | A/G | 0.339203 | 0.233544 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22457842 | AATGGTCAGGCCCCA[A/G]TCCTAGAAAGCTGAG | 9923 |
rs2001847 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22454110 | atgtgccacgacacc[C/T]ggctaattttttgtg | 9923 |
rs2007200 | snp | A/C | 0.363776 | 0.222609 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22480678 | AAAACACAGGGACTC[A/C]CATAGAGAAAAAGAA | 9923 |
rs2073168 | snp | A/G | 0.444267 | 0.157354 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22511451 | ATAAAATGAATACGT[A/G]ACTTAAGGTTGTGAT | 9923 |
rs2078450 | snp | A/G | 0.436834 | 0.166111 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22442291 | CTTGTCCTTTCTCTC[A/G]GCTAACCTTACAGAT | 9923 |
rs2143748 | snp | C/G | 0 | 0 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22469850 | AATCCACTGCCACTA[C/G]AACTATAAGGTGGGG | 9923 |
rs2235884 | snp | C/G | 0.0356815 | 0.128715 | utr-variant-3-prime, nc-transcript-variant | ZBTB40 | GRCh38.p7 | 1:22529373 | GCAGAGGTCTGGGGA[C/G]CCACCGAACAGATCC | 9923 |
rs2235885 | snp | A/T | 0.00953873 | 0.0683987 | utr-variant-3-prime, nc-transcript-variant | ZBTB40 | GRCh38.p7 | 1:22529304 | TGGCCTCTGGACTGA[A/T]CTCTGGGGCCTTTGG | 9923 |
rs2281353 | snp | C/G | 0.0777841 | 0.181223 | utr-variant-3-prime, nc-transcript-variant, intron-variant | ZBTB40 | GRCh38.p7 | 1:22526736 | ATGCCTCCTGGGGTA[C/G]CCTGGTCACCAGCTC | 9923 |
rs2281354 | snp | C/T | 0.362523 | 0.223246 | utr-variant-3-prime, nc-transcript-variant, intron-variant | ZBTB40 | GRCh38.p7 | 1:22526648 | CAGTGTCATAGAGGC[C/T]GCAGCAGCGGGCCTG | 9923 |
rs2281355 | snp | C/T | 0.150762 | 0.22946 | utr-variant-3-prime, nc-transcript-variant | ZBTB40 | GRCh38.p7 | 1:22526411 | GCAGGAAGGCTCTGC[C/T]GGATGAAAGGCTGCT | 9923 |
rs2870140 | snp | C/T | 0.418169 | 0.184985 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22468878 | gattgtgccactgta[C/T]tccagcctgagtgat | 9923 |
rs3066614 | in-del | -/GAA | | | intron-variant | ZBTB40 | GRCh38.p7 | 1:22517807 | GGGAAAAGGCAAATG[-/GAA]GATGGCCTAATGGAA | 9923 |
rs3754008 | snp | C/T | 0.0700422 | 0.173537 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22525374 | GCCCAGCTACTTCTC[C/T]GTGCTACAGGAGAGA | 9923 |
rs3754009 | snp | C/T | 0.0905309 | 0.192535 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22525142 | CCTACCTGACTTCCC[C/T]TCTGTTCCCCAGAGG | 9923 |
rs3754010 | snp | A/T | 0.441157 | 0.167075 | intron-variant, utr-variant-5-prime | ZBTB40 | GRCh38.p7 | 1:22510006 | GCTTTGTTTTATCTA[A/T]GTTTATCTTGGCTCT | 9923 |
rs4233289 | snp | A/C | 0.494936 | 0.050064 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22463962 | GTTTTGAAAACAAAC[A/C]TTTCTAGTGGTCCTT | 9923 |
rs4268328 | snp | A/C | 0.322007 | 0.239405 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22462853 | AGTTGTCTATGAATT[A/C]TTTTCTTTTAAAAAA | 9923 |
rs4354513 | snp | C/G | 0.154329 | 0.23097 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22438731 | taatgagtgttgaca[C/G]ggtatctcattgaag | 9923 |
rs4369203 | snp | A/G | 0.472241 | 0.114494 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22468966 | TGAACAGCGAGGACT[A/G]CAGGTGTACTCCACC | 9923 |
rs4540623 | snp | C/G | 0.185472 | 0.241529 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22439488 | gtcttacatttatgt[C/G]ttcaattcattttga | 9923 |
rs4655060 | snp | A/G | 0.0573587 | 0.15934 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22441403 | aaagaaccaagtttc[A/G]gtttattttttccta | 9923 |
rs4655061 | snp | A/G | 0.445196 | 0.1562 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22441563 | tctcagctcactgca[A/G]cctccacctcctgtg | 9923 |
rs4655062 | snp | A/G | 0.186737 | 0.241863 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22441644 | taaaccactgcaccc[A/G]gctaatttttgtatt | 9923 |
rs4655063 | snp | A/G | 0.195526 | 0.243993 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22447507 | ggagctagaaaccct[A/G]aggggagaaacaggc | 9923 |
rs4655064 | snp | A/C | 0.453331 | 0.145452 | utr-variant-5-prime, intron-variant, nc-transcript-variant | ZBTB40 | GRCh38.p7 | 1:22451963 | TCGTGTCCTCTATGG[A/C]GCTGTCAATAAAGAA | 9923 |
rs4655067 | snp | C/T | 0.494896 | 0.0502606 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22487796 | TTAAAGCCTTTCAAA[C/T]GCCTCAATGGCTGCT | 9923 |
rs4655068 | snp | C/T | 0.466515 | 0.124985 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22487861 | ATGGCCTATATATCC[C/T]TCTGTGGCCAACACC | 9923 |
rs4655069 | snp | A/G | | | intron-variant | ZBTB40 | GRCh38.p7 | 1:22496933 | agtcccaaaacctca[A/G]aagtagggaaaccgg | 9923 |
rs4655070 | snp | C/T | 0.4944 | 0.0526182 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22498693 | AGATGCCACCATTGA[C/T]GAAAGCTTCCCTTCC | 9923 |
rs4655071 | snp | C/T | 0.480382 | 0.097079 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22501438 | GCCAAATGCAAGGAG[C/T]GGATGGTTCTTGTGG | 9923 |
rs4655072 | snp | A/G | 0.478685 | 0.10101 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22510695 | GTGAAAGAAAATGAC[A/G]TTTAAATGGGTACAT | 9923 |
rs5773006 | in-del | -/T | 0.187053 | 0.241946 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22461330 | CCTAGAGTTCCGTTG[-/T]TTTTTTTTTTTTTTT | 9923 |
rs6426755 | snp | A/T | 0.118235 | 0.212457 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22432090 | TAGACTCTGAACATT[A/T]CTCCCATTTTGCAGA | 9923 |
rs6426756 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22432765 | ATTCTTATATCTGCC[C/G]CCCATCACCACCATT | 9923 |
rs6426758 | snp | A/G | 0.067446 | 0.170804 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22464788 | tacacgtattcagtt[A/G]catgctggttgtttt | 9923 |
rs6657564 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22457024 | TGTGATCCCAGCACT[C/T]TGGGAGGCTGAGGCA | 9923 |
rs6659222 | snp | A/G | 0.0264051 | 0.111827 | missense, nc-transcript-variant | ZBTB40 | GRCh38.p7 | 1:22490621 | CAAACCTTTAGTGAG[A/G]CAAAGAAGACAAGCA | 9923 |
rs6659354 | snp | A/G | 0.445855 | 0.155373 | intron-variant | ZBTB40 | GRCh38.p7 | 1:22440233 | tggtggaatctttac[A/G]gttttctatatgtaa | 9923 |