SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs961194 | snp | C/T | 0.0998734 | 0.199905 | intron-variant | FAM179B | GRCh38.p7 | 14:44973788 | gtatagacttctaaa[C/T]tgatgggtttttttt | 54813 |
rs1115185 | snp | A/C | 0.339203 | 0.233544 | intron-variant | FAM179B | GRCh38.p7 | 14:44973596 | TCTCTCTCTCTCTCT[A/C]TATATATACATATAT | 54813 |
rs1510518 | snp | A/C | 0.0217236 | 0.101931 | intron-variant | FAM179B | GRCh38.p7 | 14:44975345 | CTAATACAATCTATT[A/C]ACTTATATTAGACAT | 54813 |
rs1955669 | snp | C/G/T | | | utr-variant-3-prime | KLHL28 | GRCh38.p7 | 14:44926787 | tgctgggattacagg[C/G/T]gtgagccactgcgcc | 54813 |
rs1980522 | snp | G/T | 0 | 0 | missense, upstream-variant-2KB, nc-transcript-variant | FAM179B, KLHL28 | GRCh38.p7 | 14:44963335 | CCTCTGCCCTGAGGA[G/T]ACACTACAATCGCCG | 54813 |
rs2144107 | snp | C/T | 0 | 0 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | KLHL28, FAM179B | GRCh38.p7 | 14:44961178 | ACAAGGCAGAATTCT[C/T]TTAGAACCATGATGC | 54813 |
rs3036333 | in-del | -/TA | | | intron-variant | FAM179B | GRCh38.p7 | 14:44973604 | CTCTCTCTATATATA[-/TA]CATATATATATATCT | 54813 |
rs3742591 | snp | C/G | 0.109482 | 0.206782 | missense, upstream-variant-2KB, nc-transcript-variant | FAM179B, KLHL28 | GRCh38.p7 | 14:44963952 | TTTGACTTGCCCAAA[C/G]TGTCCTTTGATCTTG | 54813 |
rs3825629 | snp | C/G | 0.1839 | 0.241103 | missense, upstream-variant-2KB, nc-transcript-variant | FAM179B, KLHL28 | GRCh38.p7 | 14:44963667 | GTGCATGGCACACTT[C/G]AAGTCCTGCATTTAC | 54813 |
rs6572290 | snp | A/G | 0.313082 | 0.241911 | utr-variant-3-prime | KLHL28 | GRCh38.p7 | 14:44927962 | GATGTTAACATTGGC[A/G]TAATCACTAACATTT | 54813 |
rs6572291 | snp | A/G | 0.300926 | 0.244758 | intron-variant | KLHL28 | GRCh38.p7 | 14:44951903 | cctgttgccctggcc[A/G]gggtgtggtggcgag | 54813 |
rs7145870 | snp | A/G | 0.300926 | 0.244758 | intron-variant | KLHL28 | GRCh38.p7 | 14:44951761 | TGCTTAATCAAAACA[A/G]TGTCAACTAGCAACT | 54813 |
rs7147644 | snp | A/T | 0.127254 | 0.217792 | intron-variant | FAM179B | GRCh38.p7 | 14:44977157 | TTCTGCTTTATATAT[A/T]TGATTGATTGACTAG | 54813 |
rs7147811 | snp | A/T | 0.301429 | 0.244653 | intron-variant | FAM179B | GRCh38.p7 | 14:44977228 | TGAAGAAAATTAGAC[A/T]GACtttttttttttt | 54813 |
rs7151557 | snp | C/T | 0.322959 | 0.239117 | utr-variant-3-prime | KLHL28 | GRCh38.p7 | 14:44926663 | AGGTACCTGCCACAA[C/T]GCCCAGCTAATTTTT | 54813 |
rs7154959 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | KLHL28 | GRCh38.p7 | 14:44939452 | ctaattttccaagtc[C/T]ttctgttccgcttac | 54813 |
rs7155135 | snp | A/C | 0.0209421 | 0.100162 | utr-variant-3-prime | KLHL28 | GRCh38.p7 | 14:44926996 | AGTCTGGGCCAACTA[A/C]AATAGTGCACCTATT | 54813 |
rs7158846 | snp | A/G | 0.306431 | 0.243548 | intron-variant | KLHL28 | GRCh38.p7 | 14:44954423 | AAAAGGCAACTGAcc[A/G]agatttttaaaacaa | 54813 |
rs7492473 | snp | A/G | 0 | 0 | intron-variant | KLHL28 | GRCh38.p7 | 14:44946020 | AATAATCAGATTTGT[A/G]ATTTATTTGTCTGTT | 54813 |
rs8010366 | snp | A/G | 0.103438 | 0.202533 | intron-variant | KLHL28 | GRCh38.p7 | 14:44946823 | ggcttctcaaagtgc[A/G]gggattacaggcatg | 54813 |
rs8017081 | snp | G/T | 0.312593 | 0.242037 | intron-variant | KLHL28 | GRCh38.p7 | 14:44932257 | GAGAGGGGTGGGGGG[G/T]GGGGAGAAAAACCTT | 54813 |
rs8018380 | snp | C/T | 0.383439 | 0.21141 | intron-variant | KLHL28 | GRCh38.p7 | 14:44941402 | TGTGGAAGGCTGAGG[C/T]GGGCAGATCACCTGA | 54813 |
rs9323106 | snp | C/T | 0.309401 | 0.24284 | intron-variant | FAM179B | GRCh38.p7 | 14:44977568 | TAGAAAAATTCATAG[C/T]TCTTCCTATGAGACC | 54813 |
rs10129173 | snp | G/T | 0.307671 | 0.243257 | intron-variant | FAM179B | GRCh38.p7 | 14:44972067 | aaccagatctcttga[G/T]aactcactattatga | 54813 |
rs10129201 | snp | A/G | 0.109108 | 0.206518 | intron-variant | KLHL28 | GRCh38.p7 | 14:44950969 | TAAAGAGACATATGA[A/G]CCATTTTAAAATATA | 54813 |
rs10129456 | snp | A/G | 0.0923359 | 0.194016 | utr-variant-3-prime | KLHL28 | GRCh38.p7 | 14:44928404 | GGCCCCAAATATCAT[A/G]ATAATAAAAGCAATT | 54813 |
rs10131595 | snp | A/T | 0.109108 | 0.206518 | intron-variant | KLHL28 | GRCh38.p7 | 14:44955396 | agaacacttctagca[A/T]tcagatgtactctct | 54813 |
rs10135494 | snp | C/T | 0.109814 | 0.206997 | intron-variant | KLHL28 | GRCh38.p7 | 14:44943825 | gcctaagcaatcctc[C/T]tgcctcagcctcctg | 54813 |
rs10136688 | snp | C/T | 0 | 0 | intron-variant | FAM179B | GRCh38.p7 | 14:44969149 | cttccttccttcctt[C/T]ctttcttTCttttct | 54813 |
rs10136741 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL28 | GRCh38.p7 | 14:44948303 | AATGTACATAAAAAC[A/G]TGATAAACTGTAAGT | 54813 |
rs10136855 | snp | A/G | 0.310878 | 0.242475 | intron-variant | FAM179B | GRCh38.p7 | 14:44978556 | ATGCCTGTAATCCCA[A/G]CACTTTGGGAGGCCA | 54813 |
rs10136926 | snp | A/G | 0.314544 | 0.241524 | intron-variant | FAM179B | GRCh38.p7 | 14:44978578 | GGGAGGCCAAGGCAG[A/G]AGGATTGCTTGAGCC | 54813 |
rs10137510 | snp | A/G | 0.444444 | 0.157135 | intron-variant | KLHL28 | GRCh38.p7 | 14:44941646 | aaaaaaaaaaaaaaa[A/G]aaaaagaaaaagaaa | 54813 |
rs10139998 | snp | A/G | 0.314544 | 0.241524 | intron-variant | FAM179B | GRCh38.p7 | 14:44979361 | ctctgcttcatagac[A/G]gcaccttcttgctgt | 54813 |
rs10140013 | snp | C/T | 0.300926 | 0.244758 | intron-variant | KLHL28 | GRCh38.p7 | 14:44940078 | GGAAGGGTCATCCCA[C/T]GATGGAAGACATCAC | 54813 |
rs10140049 | snp | A/G | 0.311123 | 0.242413 | intron-variant | FAM179B | GRCh38.p7 | 14:44979195 | aataataataataCT[A/G]TTTTCAAAGGCAGCT | 54813 |
rs10140108 | snp | C/T | 0.305934 | 0.243663 | intron-variant | KLHL28 | GRCh38.p7 | 14:44940191 | ATAACTAACCTACTC[C/T]CACAATAATAGCATT | 54813 |
rs10142624 | snp | A/G | 0.109461 | 0.206758 | intron-variant | KLHL28 | GRCh38.p7 | 14:44955657 | tggatgtggtggcac[A/G]tgcctgtagtctcag | 54813 |
rs10142928 | snp | A/G | 0.100944 | 0.200705 | intron-variant | KLHL28 | GRCh38.p7 | 14:44955659 | gatgtggtggcacat[A/G]cctgtagtctcagct | 54813 |
rs10145267 | snp | C/G | 0.299916 | 0.244966 | intron-variant | KLHL28 | GRCh38.p7 | 14:44955769 | ccagcctgggagaca[C/G]agtgaggccctgcct | 54813 |
rs10147547 | snp | A/G | 0.109814 | 0.206997 | intron-variant | KLHL28 | GRCh38.p7 | 14:44939181 | tagaatgtggagagc[A/G]gactcccaaggtggc | 54813 |
rs10147950 | snp | A/C | 0.104149 | 0.203046 | intron-variant | KLHL28 | GRCh38.p7 | 14:44939597 | ccataaagtcctagg[A/C]aactgatgcaattca | 54813 |
rs10149484 | snp | C/T | 0.311369 | 0.242351 | intron-variant | FAM179B | GRCh38.p7 | 14:44971614 | tttgctcttcctttg[C/T]tagtttcctaggatg | 54813 |
rs10149748 | snp | C/G | 0.109814 | 0.206997 | intron-variant | KLHL28 | GRCh38.p7 | 14:44944764 | aaaaagaaagaaaga[C/G]agaaaATGGAATAAA | 54813 |
rs10152101 | snp | A/C | 0.293551 | 0.246177 | intron-variant | KLHL28 | GRCh38.p7 | 14:44951108 | AAAAGGGGCTGGCCC[A/C]ATGAAAACTATGGCT | 54813 |
rs11157423 | snp | A/T | 0.302435 | 0.244439 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | KLHL28, FAM179B | GRCh38.p7 | 14:44960986 | TCATTCAAAAGTAAT[A/T]GTATTATTCCTTCAA | 54813 |
rs11157424 | snp | A/C | 0.302435 | 0.244439 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | KLHL28, FAM179B | GRCh38.p7 | 14:44961013 | TCAAAAAAAAAAAAT[A/C]TCTCTTCCACACTCC | 54813 |
rs11626430 | snp | G/T | 0 | 0 | utr-variant-3-prime | KLHL28 | GRCh38.p7 | 14:44928828 | TTCTCTTTTTTCTTT[G/T]TGATTATTGATTTAC | 54813 |
rs11627736 | snp | A/C | 0 | 0 | upstream-variant-2KB | KLHL28, FAM179B | GRCh38.p7 | 14:44962033 | CCTTCTCCGCTGTAG[A/C]TGCGTTTACAACGTT | 54813 |
rs11845904 | snp | A/G | 0.324382 | 0.238678 | intron-variant | KLHL28 | GRCh38.p7 | 14:44935125 | tgccatatcatataa[A/G]agaatactacatggc | 54813 |
rs11846502 | snp | C/T | 0.131381 | 0.220067 | intron-variant | KLHL28 | GRCh38.p7 | 14:44930646 | ctttagatttttgaa[C/T]ttggcatgatcaacc | 54813 |
rs11846656 | snp | C/T | 0.24134 | 0.24985 | intron-variant | FAM179B | GRCh38.p7 | 14:44977984 | AACTGGGCAGCACCA[C/T]GTGAGCTGATTTAAG | 54813 |
rs11846891 | snp | C/G | 0.137867 | 0.223442 | intron-variant | FAM179B | GRCh38.p7 | 14:44978504 | CTGATAGAAGCAGTA[C/G]TTACTAAAAGAAGAT | 54813 |
rs11847071 | snp | A/G | 0.118933 | 0.212888 | intron-variant | FAM179B | GRCh38.p7 | 14:44965855 | tttattacactgggg[A/G]cttacaaatagtaat | 54813 |
rs11848799 | snp | C/T | 0.226779 | 0.248919 | intron-variant | KLHL28 | GRCh38.p7 | 14:44946394 | TCATATTAACATACT[C/T]TACCCAAAATTTCAA | 54813 |
rs11850346 | snp | G/T | 0.0894459 | 0.191631 | intron-variant | FAM179B | GRCh38.p7 | 14:44974333 | tgttacagtgttttt[G/T]atttctaggtttctt | 54813 |
rs11850363 | snp | A/G | 0.310878 | 0.242475 | intron-variant | FAM179B | GRCh38.p7 | 14:44974624 | TAGTTTTTTAGTAAT[A/G]TACTGTTAAGGTGTG | 54813 |
rs11851962 | snp | C/T | 0.314301 | 0.241589 | intron-variant | KLHL28 | GRCh38.p7 | 14:44933524 | AAAGGTTCAGAATTA[C/T]GATTAATTTCTCATA | 54813 |
rs12147161 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | KLHL28, FAM179B | GRCh38.p7 | 14:44961016 | AAAAAAAAAAATATC[C/T]CTTCCACACTCCAAA | 54813 |
rs12184988 | snp | A/G | | | intron-variant | FAM179B | GRCh38.p7 | 14:44966010 | gtcctgagtagctga[A/G]attacaggctcccac | 54813 |
rs12590192 | snp | A/G | 0 | 0 | intron-variant | KLHL28 | GRCh38.p7 | 14:44956784 | atatattaattaatc[A/G]ctgctattttttgtt | 54813 |
rs12883482 | snp | G/T | 0 | 0 | intron-variant | KLHL28 | GRCh38.p7 | 14:44942877 | ATTATTTTCTACATG[G/T]CTCCTTTACTAAATT | 54813 |
rs17115690 | snp | C/T | 0.105569 | 0.204058 | downstream-variant-500B | KLHL28 | GRCh38.p7 | 14:44924292 | AAAGTTAGCTTGGTT[C/T]AGTTCACAATTATCA | 54813 |
rs17115692 | snp | C/T | 0.124144 | 0.21601 | utr-variant-3-prime | KLHL28 | GRCh38.p7 | 14:44926072 | TTTGATCCTTTTTAA[C/T]ATAGAAACATGTGGC | 54813 |
rs17115694 | snp | C/G | 0.167158 | 0.235875 | utr-variant-3-prime | KLHL28 | GRCh38.p7 | 14:44926135 | TAATGAAACTTCTCA[C/G]AAATTTGTAAAAGAA | 54813 |
rs17115703 | snp | A/C | 0.221439 | 0.248363 | intron-variant | KLHL28 | GRCh38.p7 | 14:44947715 | AAATCCAACTCTTGA[A/C]ATTTTTATCTTTGTC | 54813 |
rs17115714 | snp | A/T | 0.109461 | 0.206758 | intron-variant | KLHL28 | GRCh38.p7 | 14:44958055 | TCAGGTTCCTCCATA[A/T]CTCTGCCATAGTTTT | 54813 |
rs17115718 | snp | C/G | 0.306182 | 0.243605 | intron-variant | FAM179B | GRCh38.p7 | 14:44975180 | TTCATTAGCCACTTT[C/G]ACACAGATCAACTGA | 54813 |
rs17115721 | snp | C/G | 0.0998734 | 0.199905 | intron-variant | FAM179B | GRCh38.p7 | 14:44976105 | AACCCACCTTTCAGA[C/G]TTCTCAAATCTCACC | 54813 |
rs17854942 | snp | G/T | | | synonymous-codon | KLHL28 | GRCh38.p7 | 14:44945914 | AAGCATGTAGGTCGG[G/T]GATGTGTGGTCCATC | 54813 |
rs28499068 | snp | A/T | | | intron-variant | FAM179B | GRCh38.p7 | 14:44968214 | TTTATGTGTGCAGTT[A/T]AAAAAAAGTATATAT | 54813 |
rs28513220 | snp | C/T | 0.0919752 | 0.193722 | intron-variant | KLHL28 | GRCh38.p7 | 14:44933828 | TAGATGTACACACCA[C/T]ACAAAATCTAAAGTT | 54813 |
rs28544334 | snp | C/T | 0.102726 | 0.202016 | intron-variant | KLHL28 | GRCh38.p7 | 14:44930157 | AGAAACAAATTATAG[C/T]AAACACTAAAACAGT | 54813 |
rs28558522 | snp | A/C | 0.305685 | 0.24372 | intron-variant | KLHL28 | GRCh38.p7 | 14:44950034 | TACAGGTAATGGAAC[A/C]GAGGTACTGAGTCTG | 54813 |
rs28690299 | snp | A/C | 0.103438 | 0.202533 | intron-variant | KLHL28 | GRCh38.p7 | 14:44949676 | AAGGATCCTGAAAGA[A/C]TTATATCTAACAAGA | 54813 |
rs28695721 | snp | C/T | 0.300926 | 0.244758 | intron-variant | KLHL28 | GRCh38.p7 | 14:44942638 | CTTCTGAATACCAAT[C/T]AGCTTTTAGTTTCCT | 54813 |
rs28802144 | snp | A/G | 0.0995161 | 0.199636 | intron-variant | FAM179B | GRCh38.p7 | 14:44972729 | GGTGTACCTTTCTCC[A/G]TCTCTTTACTTTTAA | 54813 |
rs28831119 | snp | A/C | 0.0995161 | 0.199636 | intron-variant | FAM179B | GRCh38.p7 | 14:44972631 | AGGCCCCTCTTTATC[A/C]CTGATAACTTTTCTT | 54813 |
rs28927673 | snp | A/C/G/T | 0.0109292 | 0.0731104 | synonymous-codon, nc-transcript-variant | FAM179B | GRCh38.p7 | 14:44964053 | AAGGATGCTGGTTTT[A/C/G/T]CCTGAGCCCATTGAT | 54813 |
rs34089963 | in-del | -/T | 0.5 | 0 | intron-variant | FAM179B | GRCh38.p7 | 14:44975790 | CTTTTTTTTTTTTTT[-/T]AATGAAGTGGGTTTG | 54813 |
rs34191093 | in-del | -/T | | | intron-variant | KLHL28 | GRCh38.p7 | 14:44952748 | ACTGTGACTATATTT[-/T]GGTTCTCAGCTATCT | 54813 |
rs34218546 | in-del | -/T | | | utr-variant-3-prime | KLHL28 | GRCh38.p7 | 14:44925360 | ATATATTTAAAATTT[-/T]CTATAGTTTTCTTAC | 54813 |
rs34356539 | in-del | -/C | | | intron-variant | KLHL28 | GRCh38.p7 | 14:44938256 | AAGTTATTTACTTCC[-/C]AAAACACAATGGTGA | 54813 |
rs34373760 | snp | A/G | 0.00220969 | 0.0331657 | missense | KLHL28 | GRCh38.p7 | 14:44934170 | TGTTTTGCTGCAGCG[A/G]TATTGGATGGAATGA | 54813 |
rs34466372 | in-del | -/G | | | intron-variant | KLHL28 | GRCh38.p7 | 14:44948119 | AGAATGAATAACAGG[-/G]AAAGGCAAGTAGATA | 54813 |
rs34596250 | in-del | -/C | | | intron-variant | KLHL28 | GRCh38.p7 | 14:44932146 | TCTGCCTCAGCCTCC[-/C]TGAGTAGCTAGGACT | 54813 |
rs34684144 | in-del | -/T | | | intron-variant | KLHL28 | GRCh38.p7 | 14:44947945 | AGTAGGTACTTTTTT[-/T]CCAGAACATAATATA | 54813 |
rs34924029 | in-del | -/G | | | intron-variant | FAM179B | GRCh38.p7 | 14:44973648 | GACCTATATAATTTT[-/G]CCTTTTCTCTGAAAA | 54813 |
rs35122417 | in-del | -/C | | | intron-variant | KLHL28 | GRCh38.p7 | 14:44957113 | CAGGTGTGAGCCCCC[-/C]ATGACCAGCTGTATT | 54813 |
rs35237680 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | KLHL28 | GRCh38.p7 | 14:44953360 | TATTAGAATAAAATA[C/T]GGGTAAAAACTTATG | 54813 |
rs35264118 | in-del | -/C | | | intron-variant | KLHL28 | GRCh38.p7 | 14:44941718 | AAGAGCCACTTTTCC[-/C]ATTTTTATCTTTCTG | 54813 |
rs35338558 | in-del | -/C | | | intron-variant | FAM179B | GRCh38.p7 | 14:44967894 | TTATATGTTATTTCC[-/C]TTGTATTATAAGCAT | 54813 |
rs35352691 | snp | A/C | 0.00370171 | 0.042862 | missense | KLHL28 | GRCh38.p7 | 14:44934256 | GACAATCTTATTTAC[A/C]ATCTGTAGAGAAGTA | 54813 |
rs35428986 | in-del | -/AT | 0.100231 | 0.200173 | intron-variant | FAM179B | GRCh38.p7 | 14:44964688 | TTAAATTTGAGACAC[-/AT]GTGATATAGACAATA | 54813 |
rs35493028 | in-del | -/C | | | intron-variant | KLHL28 | GRCh38.p7 | 14:44948092 | AAAGTTAAAATCTAG[-/C]ACTTAAAAGTAAAGA | 54813 |
rs35612892 | in-del | -/G | | | intron-variant | FAM179B | GRCh38.p7 | 14:44971589 | TTCTCCTGCTCACTT[-/G]TGGATTTAATTTGCT | 54813 |
rs35728857 | snp | A/G | 0.0075861 | 0.0611187 | missense | KLHL28 | GRCh38.p7 | 14:44934413 | CGTCCTGGCGTCACT[A/G]TCAGAAAACATGAAA | 54813 |
rs35780816 | in-del | -/A/AA | 0 | 0 | intron-variant | FAM179B | GRCh38.p7 | 14:44964973 | AAAAAAAAAAAAAAA[-/A/AA]GGAAAAAGAAAAAGC | 54813 |
rs35910931 | in-del | -/G | | | utr-variant-3-prime | KLHL28 | GRCh38.p7 | 14:44927387 | TTAACAATAGTCTAG[-/G]AACATTATGGCACTT | 54813 |
rs56821474 | in-del | -/ATAT/ATATAT/ATATATATATATATATATATATATATATAT | 0 | 0 | intron-variant | KLHL28 | GRCh38.p7 | 14:44935903 | TGTATATATATATAT[lengthTooLong]CTTTACCCTCCCCCC | 54813 |