SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs201971360 | snp | A/G | 0.00230745 | 0.0338881 | intron-variant | G2E3 | GRCh38.p7 | 14:30612404 | TTCTATTAATATATG[A/G]CTCTTTCAAATTACA | 55632 |
rs201972229 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30598660 | CTTCTGCTGAGAAAG[C/T]AGATTTTATAGTTAG | 55632 |
rs202239680 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30603942 | AGAATATTAAGTACT[C/T]TTTCAAAATGTGAAG | 55632 |
rs367593383 | in-del | -/TAAA | | | intron-variant | G2E3 | GRCh38.p7 | 14:30581345 | TGGTTCGTATCTCAA[-/TAAA]ACAGTTATTTAAAGG | 55632 |
rs367674874 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | G2E3 | GRCh38.p7 | 14:30592545 | TAAATTTTCTGTTTA[C/G]AGCATCAGAGTTTAG | 55632 |
rs367755885 | snp | A/G | 2.86537e-05 | 0.00378497 | intron-variant | G2E3 | GRCh38.p7 | 14:30605840 | TTTATTGTTGTATAT[A/G]CCAAATATCACATGT | 55632 |
rs367825065 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30595933 | CTTGGATTTTTCCAT[A/C]ATTGCTCTAGTCTTG | 55632 |
rs367839066 | snp | C/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30612298 | GTCTCAGACTTATAA[C/T]GACATTAAGTGATAA | 55632 |
rs367882021 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30574777 | TTTTTATGGCTGCAC[A/G]ATATTTTATCGTGTA | 55632 |
rs367886482 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30600457 | GTGACCCTGATTATT[C/T]ATTCGTTAACACCAA | 55632 |
rs368005719 | snp | C/G | 1.64754e-05 | 0.00287009 | intron-variant | G2E3 | GRCh38.p7 | 14:30598627 | GTTCAGTTGTGCTTA[C/G]TGGTTCCTTGTTTAA | 55632 |
rs368040561 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30611691 | GAGATAAGGTCTCAG[C/T]CTGTCACCCAGGCTG | 55632 |
rs368220764 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30596368 | AGGGCCTTAGTCCCT[A/G]TCAATTTATTCTTCA | 55632 |
rs368398696 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30574207 | CCCCTTAATGCTTCA[C/G]TATTTCCTAAGAACA | 55632 |
rs368588898 | snp | A/C/T | 1.75616e-05 | 0.00296319 | intron-variant | G2E3 | GRCh38.p7 | 14:30612400 | TTGTTTCTATTAATA[A/C/T]ATGGCTCTTTCAAAT | 55632 |
rs368652763 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30561490 | GTACCAACTTCTCTT[C/T]CCAAGGACCATCTTC | 55632 |
rs368669388 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30585710 | TTATATCTACTCTAA[C/T]CTTTATTTTTTTGTT | 55632 |
rs368674081 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30613639 | TCATGGTATCTAGAC[C/G]TTTTCATTGAACCCA | 55632 |
rs368732441 | snp | G/T | 3.58198e-05 | 0.00423186 | intron-variant | G2E3 | GRCh38.p7 | 14:30592462 | CGTGAGTTATTTAAC[G/T]GTTAAATATGAAAGT | 55632 |
rs368854800 | snp | C/G | 1.66718e-05 | 0.00288715 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30602001 | TTTAAATCTGTAGGA[C/G]AGTTCCAAAAAGCCA | 55632 |
rs368859638 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30575312 | CTTATAAATGCTTTT[G/T]ATAAAATTCAGCAGC | 55632 |
rs368883056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30581860 | CTTGCTACAATGAAA[C/T]ATGAGGAATTTAAAT | 55632 |
rs368888525 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30604910 | CATTCATTCATTCAT[G/T]TATGAGACGGAGTTT | 55632 |
rs368934954 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30570028 | TACTTGCCTGCCTCC[C/T]ATGTGAGTATGTGTA | 55632 |
rs369165140 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30582508 | TGTACCTCCATCCAG[C/G]GTTCATGGCAAGAGT | 55632 |
rs369211237 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30563674 | TTGATAACTTAATGT[A/G]AACTTGTAACTTTGT | 55632 |
rs369270598 | snp | A/G | 1.79213e-05 | 0.00299338 | intron-variant | G2E3 | GRCh38.p7 | 14:30592463 | GTGAGTTATTTAACT[A/G]TTAAATATGAAAGTT | 55632 |
rs369374564 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30587417 | TTACCACCTTAGCAT[G/T]CCAGGCTTGCATTAG | 55632 |
rs369393450 | in-del | -/GTT | | | intron-variant | G2E3 | GRCh38.p7 | 14:30596095 | TTTCAATAACCTGTT[-/GTT]TCCCTCCCTTATATG | 55632 |
rs369503438 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30570898 | CTTTATCAGATTATG[A/G]TTTGCAAATACTTTC | 55632 |
rs369525078 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30597108 | TCATTTTTTTCTCAC[A/G]TTTTAAAGGGCAACA | 55632 |
rs369571930 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30592517 | TACATATCCCAATGA[C/T]ATAATACTACAATAA | 55632 |
rs369580395 | in-del | -/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30598870 | TAGCCACATGTGGCT[-/G]GTTGAGCACTTGAGA | 55632 |
rs369642570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30605138 | TGACCTCAGGTGATC[C/T]GCCTGCCTCTGCCTC | 55632 |
rs369748124 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30581603 | GCTACTCGCTAGGCC[A/G]AGGCAGGAGAATCGC | 55632 |
rs369803145 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30570415 | TTTGGCTATTATTTC[A/T]TCAAACATTCTTTCT | 55632 |
rs369817987 | snp | A/C | 1.66297e-05 | 0.0028835 | synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616444 | TCCCATCACCAATAC[A/C]TATAAAGAGTTTCAA | 55632 |
rs369834671 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30618938 | TATTGCAATTGCCTA[A/T]ATGTTGTATATTTTA | 55632 |
rs369883009 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30564576 | TAGCCTCAAGCGATC[C/T]TTCCACCTCAGCCTC | 55632 |
rs370086282 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30591574 | CCTAGCTTCACATGG[C/G]TGCTGGCAACCTTTG | 55632 |
rs370195409 | in-del | -/CCC | | | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558329 | TGGCAACATCAATCA[-/CCC]CAGCCATAAAGGTCA | 55632 |
rs370198187 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30571660 | TTATTTCAATACTAT[A/T]TATTGAATAGACTAC | 55632 |
rs370229233 | snp | A/G | 0.000229218 | 0.0107031 | utr-variant-5-prime, missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30586733 | CTTGTGTTTTCTGTC[A/G]AAAACATGATGACTG | 55632 |
rs370243413 | in-del | -/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30562996 | AGCCTGGCATTTGGG[-/G]CCACTACCAGTCTCC | 55632 |
rs370250207 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30585487 | TATATATTTATTTCT[A/G]GACTCTTCTTTTTCA | 55632 |
rs370276428 | in-del | -/A/AA | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30577223 | GCAAGACTCTGTCTC[-/A/AA]AAAAAAAAAAAAAAA | 55632 |
rs370299141 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30565713 | GTTGCCCAGGCTGGA[A/G]TGCAGTGGCACAATC | 55632 |
rs370371840 | snp | G/T | 0.000153988 | 0.00877328 | intron-variant | G2E3 | GRCh38.p7 | 14:30612181 | AGTAAATGAGTAAAG[G/T]GGCTGTATTTTCTCC | 55632 |
rs370382006 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30607343 | ATAAAGTATACTTAC[A/G]CAAACCTAGTTGGTG | 55632 |
rs370392584 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30583932 | TTTAGTACATTTACA[A/G]TGTTGTGAAACCATC | 55632 |
rs370398317 | snp | G/T | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30577157 | TTGAACCCAGGAGGC[G/T]GAGGTTGCAGTGAGC | 55632 |
rs370460196 | in-del | -/T | 0.386123 | 0.209692 | intron-variant | G2E3 | GRCh38.p7 | 14:30560111 | TTTATTGTTTTGGGC[-/T]TTTTTTTTTTTTAAT | 55632 |
rs370482758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30613033 | ACCTTTTATCTGCTG[A/G]GTAATACATATATTG | 55632 |
rs370503701 | snp | A/G | 0.000269574 | 0.0116066 | intron-variant | G2E3 | GRCh38.p7 | 14:30593642 | AGACTGTTTACAGGT[A/G]AGATACATATTTTGT | 55632 |
rs370548768 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30580161 | ATCCTGGCAAATGCA[A/C]CAGCCACAAATACGG | 55632 |
rs370636611 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30589056 | TAATTGTAGGTGTTC[C/G/T]TTCTTTCTTTTTTTC | 55632 |
rs370819316 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30607719 | TATATTCAGAAAAAT[G/T]TGTCTTTTTTTATAT | 55632 |
rs370911136 | in-del | -/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30614832 | TTCATTTTCCCTATT[-/T]GATCTTTCAGAAGAA | 55632 |
rs370916294 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30574711 | TTACTGTGCTAAGGA[C/T]AATAGCCTCCGGCTC | 55632 |
rs370926075 | in-del | -/CTTA | | | intron-variant | G2E3 | GRCh38.p7 | 14:30566516 | AAATGGAATTGTTTA[-/CTTA]ATTTCCTTTTTGGAT | 55632 |
rs370957754 | snp | A/C | 0.000150176 | 0.00866404 | intron-variant | G2E3 | GRCh38.p7 | 14:30598471 | AAGCATATTTTATAT[A/C]TTCTTTTATAGAGAT | 55632 |
rs370975001 | snp | A/G | 0.00597247 | 0.0543191 | utr-variant-3-prime, downstream-variant-500B | G2E3 | GRCh38.p7 | 14:30619785 | GATTAACCAAAAAGC[A/G]TGACATTTATAACAA | 55632 |
rs370978269 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30572461 | TTGTATCTGTTGACA[C/T]TGTGTCACAGTACAG | 55632 |
rs371023574 | snp | C/T | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30577562 | TCTAACATGGCTTAT[C/T]CACATAACAGAAGGT | 55632 |
rs371042047 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30579148 | AGAATTACTAGTGCC[A/T]CTAAAAGGAAGAAAA | 55632 |
rs371061212 | snp | A/G | 1.68012e-05 | 0.00289833 | synonymous-codon, intron-variant | G2E3 | GRCh38.p7 | 14:30605748 | GAGTCTCTTAATGCA[A/G]CATCTTGAGAACTCA | 55632 |
rs371118796 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30583270 | AAGATTAGTTATTAT[A/G]CTAACATTTGGTTCT | 55632 |
rs371119079 | snp | C/T | 3.36774e-05 | 0.00410336 | intron-variant | G2E3 | GRCh38.p7 | 14:30598435 | TTCCTGATCCTCTTA[C/T]GTAACATTATTTATA | 55632 |
rs371178505 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | G2E3 | GRCh38.p7 | 14:30583817 | TTAACTCAGGTCTCT[C/T]TGACTCTTCAAGTTG | 55632 |
rs371193633 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30590204 | ATGATTTTCATGGGG[A/G]AGCATTTTGGGTGAT | 55632 |
rs371193787 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | G2E3 | GRCh38.p7 | 14:30569182 | AAAAGAAAAAGCCCC[C/T]ACCCCTTCTCTCTCC | 55632 |
rs371320046 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30612319 | TAAGTGATAAATATA[C/T]GTTAGTAAAAGACAT | 55632 |
rs371334227 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30568000 | TGAGAAGAATGTTTC[A/G]TTCTGTTGTAGGGTG | 55632 |
rs371381534 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30598939 | ACCAAAGACTTAGTT[C/G]ACTAGGGCTGCCATT | 55632 |
rs371414775 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | G2E3 | GRCh38.p7 | 14:30619238 | TTGATTACCAGCATG[A/C]GAATTCACCTTGGTT | 55632 |
rs371500807 | in-del | -/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30574424 | ATCTTTTTTTTTTAA[-/C]TTTTTTTTTTTTTTA | 55632 |
rs371615448 | snp | A/C | 0.00478085 | 0.0486577 | upstream-variant-2KB, intron-variant | SCFD1, G2E3 | GRCh38.p7 | 14:30620433 | GAGCAAAATTGGGCT[A/C]TCAGACATTTTATAT | 55632 |
rs371641829 | snp | A/G/T | 7.22483e-05 | 0.00600996 | intron-variant | G2E3 | GRCh38.p7 | 14:30612430 | TTACATGTTTAAAGT[A/G/T]GTTAATTATCTTGTA | 55632 |
rs371712779 | in-del | -/ATA | 0.000743231 | 0.019263 | intron-variant | G2E3 | GRCh38.p7 | 14:30601959 | TAAAAGTTTTTACCT[-/ATA]ATATCTCTATTATGC | 55632 |
rs371822702 | snp | C/T | 3.29924e-05 | 0.00406142 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30615474 | TTAGTGAGCTTTTTA[C/T]AGTACACACATTACC | 55632 |
rs371836695 | snp | G/T | 6.59283e-05 | 0.00574106 | intron-variant | G2E3 | GRCh38.p7 | 14:30601766 | CTTTTCTTTGTGTCC[G/T]CAGCAAATGGGAAAT | 55632 |
rs371855590 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | G2E3 | GRCh38.p7 | 14:30574851 | TTAGGCTGATTCCAC[A/G]TCTTTGCTATTGTGA | 55632 |
rs371940182 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30609454 | CAATATTTTATTTAA[C/T]ATTGTACTTCCTCCT | 55632 |
rs371962276 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30563137 | CCGATCCTGTGGGGC[A/T]GGTCCCTACACTCTT | 55632 |
rs372178479 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30594900 | CTGGGAGGCCGAGGA[C/G]GGCGGATCACCTGAG | 55632 |
rs372250000 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30608224 | AGTTCTGAACCAGTT[-/A]AAAGATAGTTTTAAA | 55632 |
rs372421398 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | G2E3 | GRCh38.p7 | 14:30585617 | GTCTAGTTAAAGGTT[C/T]ATCAGTTTTGTTGAT | 55632 |
rs372511580 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30614731 | CAGGCAAAAATGATA[C/T]GTTTGTTCTTTGCTT | 55632 |
rs372568601 | snp | C/T | 0.000292601 | 0.0120919 | intron-variant | G2E3 | GRCh38.p7 | 14:30593661 | TACATATTTTGTAAG[C/T]TTTCTCTGATTGATA | 55632 |
rs372572407 | in-del | -/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30579908 | TAACATTTCTAGTAG[-/G]CTGTTCATATACCCT | 55632 |
rs372607268 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30572448 | GTCAGATGCCCTTTT[G/T]TATCTGTTGACATTG | 55632 |
rs372629410 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30604236 | GAAGAATTATCTTAC[C/T]TCCAAAGGACTTTCG | 55632 |
rs372690501 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30603049 | TGAGACAAAATAGGC[C/T]GGGCATCGTGGCTCA | 55632 |
rs372697682 | snp | A/C/T | 0.02016 | 0.0983543 | intron-variant | G2E3 | GRCh38.p7 | 14:30604911 | ATTCATTCATTCATT[A/C/T]ATGAGACGGAGTTTC | 55632 |
rs372812039 | in-del | -/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30560087 | CTTTGAGCATCTGTT[-/T]TYYTTGGGTTTTATT | 55632 |
rs372849031 | in-del | -/TTG | 0.0433465 | 0.140692 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30617397 | TTTAATCATGGGAAA[-/TTG]TTGTTGTTGTTGTTG | 55632 |
rs372901169 | snp | A/G | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30576376 | AAACCACCTCAAGAT[A/G]GATTAAAGACTTAGA | 55632 |
rs372925564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30598659 | CCTTCTGCTGAGAAA[A/G]TAGATTTTATAGTTA | 55632 |
rs373037684 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | G2E3 | GRCh38.p7 | 14:30603786 | GGAGTTCAAGCTGCA[A/G]TGAGCTATGATCATG | 55632 |
rs373042161 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30564642 | CCCAGTCAAAAATTA[A/G]CCATTTTAAAGTAGA | 55632 |
rs373070551 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | G2E3 | GRCh38.p7 | 14:30619784 | AGATTAACCAAAAAG[C/G]GTGACATTTATAACA | 55632 |
rs373073253 | snp | G/T | | | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30557255 | TTAACGGGGTCATAT[G/T]AGATATGTAAACATA | 55632 |
rs373078660 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30602085 | GAAGAGTCATCACCT[A/G]AATTACCCAGACAGT | 55632 |
rs373170756 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30596888 | ACTGGCTCTTCTTTC[C/T]AGTAGGCTTACAGTT | 55632 |
rs373199467 | snp | A/G | 3.39622e-05 | 0.00412067 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30592417 | GTGGACTTCAGAGAG[A/G]ATGTATTTTCCAGTT | 55632 |
rs373325801 | snp | A/G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30591352 | TTGCTAATGATTGAT[A/G/T]CATTTAATAATTTTT | 55632 |
rs373337608 | snp | C/G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30596133 | GTGGGTGGGTGGGTG[C/G/T]GCGTGTGTGTGTGTG | 55632 |
rs373429101 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30573203 | CATGAAAAAAAAATT[C/T]TAATAGCTTTTGACC | 55632 |
rs373587098 | snp | A/G | 4.63263e-05 | 0.00481259 | intron-variant | G2E3 | GRCh38.p7 | 14:30586829 | TGGTGAGTATAATTT[A/G]TAATTAAATTCTAGA | 55632 |
rs373606115 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30613040 | ATCTGCTGGGTAATA[C/G]ATATATTGACCGTTC | 55632 |
rs373665676 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30575580 | AGAGGAAGTCAAACT[A/C/G]TCTCTTTGCAGATTA | 55632 |
rs373867607 | in-del | -/AATTA | 0.00105331 | 0.0229248 | intron-variant | G2E3 | GRCh38.p7 | 14:30586831 | GTGAGTATAATTTAT[-/AATTA]AATTCTAGAAATTTG | 55632 |
rs373906130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30604631 | ACACTTTGTGACTTA[C/T]TGATCTAGACTAAAA | 55632 |
rs374175924 | snp | A/G | 3.43224e-05 | 0.00414247 | synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30608051 | TTCAGACTTTGATGT[A/G]GCACAGATTATAATC | 55632 |
rs374179653 | snp | A/G | | | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558143 | GGTCTCGATCTCCTG[A/G]CCTCGTGATCCACCC | 55632 |
rs374202437 | in-del | -/GTGTGTGT | | | intron-variant | G2E3 | GRCh38.p7 | 14:30573433 | TGTGTGTGTGTGTGC[-/GTGTGTGT]GTGTCTCTGTGTGTG | 55632 |
rs374249716 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | G2E3 | GRCh38.p7 | 14:30580378 | CGCCCTGCTAACTTT[G/T]TATTTTTGGTAGAAA | 55632 |
rs374286768 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30595881 | TGGTAAAAACTTTCC[A/G]CTCTGTGTCTACAGA | 55632 |
rs374380257 | snp | C/G | 4.95634e-05 | 0.00497788 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30612252 | AAGTCAATAATAAAT[C/G]AATGCTATAACTACC | 55632 |
rs374552919 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30599071 | TGAGGCCTCCCTCCT[C/T]GGCTTGCAGATGGCT | 55632 |
rs374594322 | snp | A/G | 5.22161e-05 | 0.00510934 | intron-variant | G2E3 | GRCh38.p7 | 14:30612393 | AGGTAAGTTGTTTCT[A/G]TTAATATATGGCTCT | 55632 |
rs374612776 | in-del | -/TT | 0.00398564 | 0.0444627 | intron-variant | G2E3 | GRCh38.p7 | 14:30563211 | GTAATAAAAAGTATC[-/TT]AATTCAAAATGTTAG | 55632 |
rs374664817 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30563965 | CTCAAGGGATCTGCC[C/T]GCTTCAGCCTCCCAA | 55632 |
rs374676857 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30600221 | CTACTACTTAATTGT[A/G]AAGATTCAGCTGAGG | 55632 |
rs374701530 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30579336 | ACCAATCTTAATGGC[A/G]TAGAATATTATTTTG | 55632 |
rs374800455 | in-del | -/A | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30576836 | TAAAAATGCTAGATT[-/A]AAAAAAATCAATCAA | 55632 |
rs374851129 | snp | A/G | 6.59489e-05 | 0.00574196 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30601838 | CCTGCTCCTCATTAC[A/G]GTCATGGGAGCAAAA | 55632 |
rs374865082 | snp | A/G | 3.29489e-05 | 0.00405874 | synonymous-codon, intron-variant, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30598540 | TCTGCAGCACTATGA[A/G]CGTTGTGATGTTCGA | 55632 |
rs374883684 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30559906 | GTACCGCAAAAATCC[G/T]AGACTCCTATTTAAA | 55632 |
rs374889556 | snp | A/G | | | synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30607898 | TACAGCTCTGAAAGA[A/G]AATCTTTACTATGAA | 55632 |
rs374919913 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30611892 | TCTGGCCTCAAGCAG[A/G]CCTCCCACCTCAGCC | 55632 |
rs374996044 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30594550 | AAAAAAAAATTAGCC[A/G]GGCATGGTGGCGGGT | 55632 |
rs374998846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30603898 | AGAATTTTTGTGAAA[A/G]CATTTGATAACTGGA | 55632 |
rs375083736 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30609954 | AGGCTTAGACAATTA[A/G]AATGTTGTTCTAATA | 55632 |
rs375165911 | snp | A/G | 0.000153988 | 0.00877327 | intron-variant | G2E3 | GRCh38.p7 | 14:30605828 | GTAATTATTTTATTT[A/G]TTGTTGTATATACCA | 55632 |
rs375271573 | in-del | -/CTT | | | intron-variant | G2E3 | GRCh38.p7 | 14:30596883 | TGGGGACTGGCTCTT[-/CTT]TCCAGTAGGCTTACA | 55632 |
rs375312489 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30587388 | AATTCATGCCTTAAG[A/T]TATTAGTGGCACATT | 55632 |
rs375406990 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30575688 | CAGGATGCAAAATCA[A/T]CATACAAAATTCACT | 55632 |
rs375415000 | snp | G/T | 0.000197694 | 0.00994022 | intron-variant | G2E3 | GRCh38.p7 | 14:30612421 | TCTTTCAAATTACAT[G/T]TTTAAAGTGGTTAAT | 55632 |
rs375441772 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30614441 | GCACTCAACCCATAG[A/G]TGTGCCCTCGAAATC | 55632 |
rs375457166 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30572230 | TTATTCTTATAAATA[C/T]GTTGGTAGGATTTTC | 55632 |
rs375492646 | in-del | -/CTC | | | intron-variant | G2E3 | GRCh38.p7 | 14:30609828 | AGAGTCATTTTCATA[-/CTC]CTCCATTTTCCAGTT | 55632 |
rs375502772 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30573066 | TCAAATTCCTGGGCT[C/T]AAGCAATCCTCCTGC | 55632 |
rs375540351 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30578067 | ATCTAAAAGAAATTA[C/T]GAAATTCAACTGAAA | 55632 |
rs375604170 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30566337 | AAATTGCTTTGGGGA[A/G]TATAACCATCTTAAT | 55632 |
rs375653876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30566010 | CCAGGACCATTTGTC[A/G]AAGAGACTGTTTTCT | 55632 |
rs375678714 | snp | A/T | 0.000367009 | 0.0135414 | intron-variant | G2E3 | GRCh38.p7 | 14:30589354 | CTAGTTTCTTAGAGT[A/T]TATTTTCTAATTGAG | 55632 |
rs375691900 | snp | C/T | 5.04825e-05 | 0.00502381 | intron-variant | G2E3 | GRCh38.p7 | 14:30598445 | TCTTATGTAACATTA[C/T]TTATAGGTCAAAGCA | 55632 |
rs375795652 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30602940 | ATAATCATTGTTTGC[C/G]TGTTTACTGTCAATG | 55632 |
rs375827293 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | G2E3 | GRCh38.p7 | 14:30561688 | TGCTTATAAATATAT[A/G]GTGCGAGACTGCCCT | 55632 |
rs375876145 | snp | C/T | 3.94734e-05 | 0.00444243 | intron-variant | G2E3 | GRCh38.p7 | 14:30607837 | ATAAAAAATGATGGT[C/T]ATCTTATAATAATAG | 55632 |
rs375903508 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30571604 | AGTTTTAATATATGA[C/G]GTCAATGTTCTTCCC | 55632 |
rs375926632 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30594996 | AAAAAAAATTAGCTG[A/G]GCGTGGTGGTGCACA | 55632 |
rs375927581 | in-del | -/G | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30577244 | AAAAAAAAAAAAAAA[-/G]AAAAAGAAAAAATGT | 55632 |
rs375933207 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30575185 | GATTAGTGATGTTGA[A/G]CTTTTTTTCATATGC | 55632 |
rs375933864 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30598833 | CTATTTTCTAGAGCC[A/C]CACTGTCCTATCTGG | 55632 |
rs376040583 | snp | A/G | 6.60753e-05 | 0.00574746 | synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30602096 | ACCTAAATTACCCAG[A/G]CAGTCACCTGGATCC | 55632 |
rs376052707 | in-del | -/GGA | | | intron-variant | G2E3 | GRCh38.p7 | 14:30589633 | TGGTAAGTTTTAGGA[-/GGA]CAGTTTATATTTTTG | 55632 |
rs376118044 | snp | C/T | 3.32773e-05 | 0.00407892 | synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616327 | TATTTTTGCAACTGG[C/T]TGCAGTTCCATTCCT | 55632 |
rs376393372 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30587839 | CTAGTCATCACAGCC[A/G]CACACTAATGTCACT | 55632 |
rs376397383 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30612964 | TTTAAAACTCTTACC[A/G]CATGAGCCAACTATT | 55632 |
rs376401126 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30617964 | TAAAATGTTTTAACC[A/G]TATTTTTCTTAATAC | 55632 |
rs376490500 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30596135 | GGGTGGGTGGGTGTG[C/T]GTGTGTGTGTGTGTG | 55632 |
rs376502139 | snp | C/T | 6.65026e-05 | 0.00576601 | synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30593612 | TCCTTGTTGTAAGAA[C/T]GCTTGGTTTCATAGA | 55632 |
rs376522784 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | G2E3 | GRCh38.p7 | 14:30567843 | TCTCCATATGTTTCT[C/G]AGTTTTCCAGTTTTC | 55632 |
rs376658710 | snp | C/G | 7.16769e-05 | 0.00598609 | intron-variant | G2E3 | GRCh38.p7 | 14:30593686 | TTGATATAAAATTAT[C/G]GCTTGCTGATTTAAA | 55632 |
rs376686393 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30573426 | GTGTGTGTGTGTGTG[C/T]GTGTGCGTGTGTGTG | 55632 |
rs376704586 | snp | A/T | 2.10666e-05 | 0.00324544 | intron-variant | G2E3 | GRCh38.p7 | 14:30593468 | TAAAATAATTTACAT[A/T]TTTAGGTCATTTTGT | 55632 |
rs376771101 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30581701 | AGCGAGACCCTGTAT[C/T]AAAAAAAAGAAGAAA | 55632 |
rs376838062 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30568742 | TATTTTTTGCTTATT[G/T]TACATTTATACATAA | 55632 |
rs376912170 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30563985 | CAGCCTCCCAAAGTC[C/T]TGGGATTACAGGCGT | 55632 |
rs376971485 | snp | C/G/T | 0.00199529 | 0.0315338 | intron-variant | G2E3 | GRCh38.p7 | 14:30598910 | TCCAAATTGCAAGGG[C/G/T]GCTGTAAATACATAC | 55632 |
rs377075694 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30604593 | GGTAATGCTGCTGCT[C/G]CTGCTGCTGCTGGTC | 55632 |
rs377168711 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30604912 | TTCATTCATTCATTT[A/G]TGAGACGGAGTTTCG | 55632 |
rs377207836 | snp | A/G | 1.76505e-05 | 0.00297068 | intron-variant | G2E3 | GRCh38.p7 | 14:30608079 | ATCAGGGTAAGCAAT[A/G]TATCTGTTTATTAAA | 55632 |
rs377291594 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30593767 | TTTTAAAACAGCTTT[A/C]AAGCACTTAATTTGA | 55632 |
rs377325017 | in-del | -/TA | | | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30617022 | TTCTGGGATTTGTGT[-/TA]TACTATGCATACTTT | 55632 |
rs377404749 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30597098 | CTCAGGAGTTTCATT[C/T]TTTTCTCACATTTTA | 55632 |
rs377406652 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30559168 | TGGACGAATTTGAAT[C/T]CTGTGGGCCGTTGAA | 55632 |
rs377462220 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30588655 | AAAGAGACTTAGATA[C/T]AGTCTAATCCAGTGT | 55632 |
rs377504509 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30571834 | ACATAGCTCTATAAG[A/C]AGTCATGAAATCACA | 55632 |
rs377531076 | snp | A/G | 1.6513e-05 | 0.00287336 | intron-variant | G2E3 | GRCh38.p7 | 14:30597416 | TTTTTATTTTCCACT[A/G]TAGGTTCAAGCAATA | 55632 |
rs377669237 | snp | A/T | 7.1486e-05 | 0.00597812 | intron-variant | G2E3 | GRCh38.p7 | 14:30615586 | TCTCAGAATATTTGT[A/T]TCAGCATATTTGTTG | 55632 |
rs377677745 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | G2E3 | GRCh38.p7 | 14:30583585 | GGAATAAGTTCAAGA[G/T]ATCTGTTGTACAACA | 55632 |
rs377716082 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30618650 | AATTTAGGATATTCA[A/T]GTTTTAAAGTGAAGC | 55632 |
rs377727085 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30618589 | CAATTCCTCATTTGA[C/T]TTATTTTATATATAG | 55632 |
rs377728452 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30595035 | CCCAGCTACTTAGGA[G/T]GCGGAGGCAGGAGAA | 55632 |
rs377743291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30583234 | AATAAAATTTTCTGT[A/G]TAAATAAACATGTAA | 55632 |
rs377743665 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30611361 | CAGCAGAGATTTTGA[A/G]TGAATGAAAAGAAGT | 55632 |
rs386381015 | in-del | -/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30560088 | TTTGAGCATCTGTTT[-/T]CTTTGGGTTTTATTG | 55632 |
rs386381016 | in-del | -/AA | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30577242 | AAAAAAAAAAAAAAA[-/AA]AGAAAAAGAAAAAAT | 55632 |
rs386776047 | multinucleotide-polymorphism | AG/CT | | | intron-variant | G2E3 | GRCh38.p7 | 14:30571888 | TTAAAAATGTTTTTG[AG/CT]ATTACAAGACTTTTG | 55632 |
rs386776048 | in-del | C/TTAAT | | | intron-variant | G2E3 | GRCh38.p7 | 14:30579535 | ATAAGTTTAATTTGG[C/TTAAT]CAGTCTTCATAAAAT | 55632 |
rs386776049 | in-del | CC/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30590332 | TTTAGACTTTGTTTT[CC/G]ACAGATGCCAAAGTC | 55632 |
rs397759430 | in-del | -/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30571188 | TGCTTTTTTTTTTTT[-/T]GCTATTTTAATGTGC | 55632 |
rs397762511 | in-del | -/A | | | intron-variant | G2E3 | GRCh38.p7 | 14:30604741 | GTGTAATCTCTCAAA[-/A]GACATTTTCTTATAT | 55632 |
rs397802471 | in-del | -/A | 0 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30571958 | TAAAAAAAAAAAAAA[-/A]CCTGCTGGGGATTTT | 55632 |
rs397827007 | in-del | -/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30573016 | ATGTACTTTTTTTTT[-/T]GGATGGAGGTCTCAC | 55632 |
rs397829350 | in-del | -/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30611832 | GCCTTTTTTTTTTTT[-/T]CTTTAGAGGGGGGCT | 55632 |
rs397967326 | in-del | -/GT | | | intron-variant | G2E3 | GRCh38.p7 | 14:30614249 | GATAAACATGTGTGT[-/GT]TCTTAGCTCATTTTA | 55632 |
rs398024674 | in-del | -/TGTG | 0 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30563736 | GTGTGTGTGTGTGTG[-/TGTG]ATATAGAGTCTCACT | 55632 |
rs398024675 | in-del | -/T | 0 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30578107 | GTACTTATTTTTTTT[-/T]ACTAAGGTTTTGTTT | 55632 |
rs527238700 | snp | A/G | | | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30557398 | TTATACGCTCATTAA[A/G]CCTGATTTTGTATCT | 55632 |
rs527289549 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30581776 | CAATCTTCCCAAATA[G/T]ATGCGGTCCGTTTTG | 55632 |
rs527344670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30574474 | AGGTTTGTTACATAG[A/G]TAAACAACATGTCAT | 55632 |
rs527481971 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30567629 | TCTCAATTTAAAAAT[C/T]TTTTTATTACATTAT | 55632 |
rs527492584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30609443 | GAATTTCTCTGCAAT[A/G]TTTTATTTAATATTG | 55632 |
rs527497230 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30573828 | TTACCAATCTTTTCC[A/G]GAAACACTCTCACAG | 55632 |
rs527546406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30561147 | CTCCAATTACATTGA[A/G]TTACTAAACTGTAAA | 55632 |
rs527554869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30608889 | CTGGAGGCTGAGTCA[C/T]AAGAATAATTTGAAT | 55632 |
rs527563710 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30618261 | TTTTTTGTCTCACCA[A/G]TAGTAATTGAAAGAT | 55632 |
rs527617644 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30617607 | ATGATATCTGTTATA[A/T]AAGCAATGTATAAAT | 55632 |
rs527652580 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30611205 | GCCCCACCTAGCTGC[A/G]GCAAAAGTTTGGCTA | 55632 |
rs527675808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30565885 | TCCAGGATGGTCTTG[A/G]TCTCCTGACCTCATG | 55632 |
rs527696259 | snp | A/G | 1.71012e-05 | 0.00292409 | intron-variant | G2E3 | GRCh38.p7 | 14:30612175 | CTCAAAAGTAAATGA[A/G]TAAAGTGGCTGTATT | 55632 |
rs527714319 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30615841 | ATCCTAATAATCTAT[G/T]TCATCATTTTCAATT | 55632 |
rs527737010 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30559029 | AGCCAGGTTAGCACC[C/G]AGCAGCAGCGCAGGA | 55632 |
rs527796114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30559488 | TTGCGCACGCCAGCC[A/G]GCTCTCAGTGTTGAG | 55632 |
rs527828331 | snp | C/G | | | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558458 | CAAAGACATACTGTG[C/G]TCCTCGATAAAGGAA | 55632 |
rs527832496 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30602244 | TAGTCTAGAAGAATG[C/T]TTTTCAGCCTTCAGG | 55632 |
rs527896467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30603066 | GGCATCGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 55632 |
rs527899952 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30594608 | TGAGGCGGGAGAATG[G/T]CATGAACCCGGAAGA | 55632 |
rs527906056 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30582830 | CAGAGTGAGGGAGGG[C/T]AGAGTAGTTAGGCTA | 55632 |
rs527973836 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30613126 | TAAGTTAGACAACTT[A/G]TGTATCTCCTTACAC | 55632 |
rs528017425 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30588229 | TCAGTCAGGAAAGGA[G/T]TATTTTACTTTTCTA | 55632 |
rs528022699 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616713 | AAAAAGGTTTTTTTT[A/G]TTAAAGCATACTAGT | 55632 |
rs528064129 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30557977 | GAGTGCAGTGGCGCA[A/G]TTTCTGCTCACTGCA | 55632 |
rs528215018 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30585814 | GGGATTTTCTTTTTT[A/T]ACATAGGCTTGCATG | 55632 |
rs528218363 | snp | A/T | 0.000190926 | 0.00976866 | intron-variant | G2E3 | GRCh38.p7 | 14:30593454 | TCATGAGATTTTTTT[A/T]AAATAATTTACATTT | 55632 |
rs528221077 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30571166 | TCTTGTGGGTGCTGT[A/G]GTGGGTTTGCTTTTT | 55632 |
rs528278657 | snp | A/G | 0.00141894 | 0.0265981 | intron-variant | G2E3 | GRCh38.p7 | 14:30586692 | TTTAAATATATTTTT[A/G]TATCTATTTACTTTT | 55632 |
rs528299331 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30597717 | TGTCATAAATGTCTC[A/G]TTCATTGATTTATAA | 55632 |
rs528597612 | in-del | -/A | | | intron-variant | G2E3 | GRCh38.p7 | 14:30609237 | TGTGCCCTCTTTACT[-/A]AAAAAAAAAGTATAT | 55632 |
rs528631998 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30578957 | CTTTGTTGAAAATGA[C/T]TGGAAAAATATGGAT | 55632 |
rs528668303 | in-del | -/TATCCAAAATGCTTGG | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30590873 | AGATTGAATATCCCT[-/TATCCAAAATGCTTGG]AACCAGAATTTTAGA | 55632 |
rs528683186 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30570980 | GATACTAACTTTAAG[G/T]ACAGTTTATCTTTTT | 55632 |
rs528785948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30607434 | ATAACATGTTACTGT[A/G]CTGAATACTGTAGAC | 55632 |
rs528806831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30564609 | AAAGTGCTGGAATTA[C/T]AGGTGTGAGCCACCA | 55632 |
rs528894531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30608736 | AGACAATGCAAGCCA[C/T]TTAACTTTTCTTCCT | 55632 |
rs528907037 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30594455 | AGCACTTTGGGAGGC[C/T]GAGGAGGGTGGATCA | 55632 |
rs528910545 | snp | G/T | 1.671e-05 | 0.00289045 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30593549 | CTTACCATGCACCAT[G/T]TGCTTGGAATTTATT | 55632 |
rs528958935 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30608226 | TTCTGAACCAGTTAA[A/G]AGATAGTTTTAAAAG | 55632 |
rs529023803 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30616181 | TCTGTGCCTTTCAGT[A/G]TTCCAAGTCTATTTG | 55632 |
rs529024155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30580263 | CCAAGCTAGAGTGCA[A/G]TGGTGTGATCTTGGC | 55632 |
rs529079807 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30580818 | TGTCCTATAATCCTG[G/T]CCTCTTTCCACTAAA | 55632 |
rs529096960 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30571528 | CAAACCCCAAGATCA[C/G/T]GAAGATTCTTCACTA | 55632 |
rs529119855 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30573413 | AACAACAGGATATGT[A/G]TGTGTGTGTGTGTGT | 55632 |
rs529142176 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30598172 | GGCAGATCACCCAAG[C/G]TCAGGAGTTCAAGAC | 55632 |
rs529230723 | in-del | -/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30569742 | GGACCAGCTGGTGAA[-/G]GGGGGGGATTATATT | 55632 |
rs529268148 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30579838 | GCATTATTATGTTTT[A/T]TTCTTTTCCACTTAA | 55632 |
rs529303517 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30609496 | TTCTCTCTTCTTTAA[G/T]GCTTCTTACTTCTTC | 55632 |
rs529411135 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30577877 | CACTCAGAATACCTT[G/T]TGACAGAAGGTATTA | 55632 |
rs529462073 | in-del | -/AAAG | | | intron-variant | G2E3 | GRCh38.p7 | 14:30606539 | ATAAAATGTAAAAAT[-/AAAG]AAAAAACTTTCCAAA | 55632 |
rs529491540 | in-del | -/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30572720 | TAAGATATATTATCC[-/T]TTTTTTTTTTAATTA | 55632 |
rs529545055 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558058 | GCTGGGACTACAGGC[G/T]CCTGCCATCACGCCC | 55632 |
rs529575960 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558786 | TCTTGCTGCTGCTGC[G/T]GTTTCCTCGAGGATG | 55632 |
rs529599348 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30600620 | GTATACCATTGGTCT[C/T]TCAATCAGTAGCTAC | 55632 |
rs529630886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30570200 | CTCTTAATCTTATTG[A/G]GGATATTTTGTATGT | 55632 |
rs529646523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30562739 | CAATGGTCACACTCC[C/T]CGTCTGCCTTCATGT | 55632 |
rs529728844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30606311 | ACTTAAGGTAATTAT[A/G]ACAGGCATCTCAAAA | 55632 |
rs529852708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30599418 | TTTTTTAGTAGAGAT[C/T]GGGTTTCACCATGTT | 55632 |
rs529863808 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30591668 | ATATGCCTGTGTCTT[A/C]AATCTCCCTCTCCTT | 55632 |
rs529923297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30584578 | AGCTATCCTTGTGAG[C/T]GTGAAGTGGTATCTC | 55632 |
rs529980310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30592010 | GTGTTTATGTATATA[A/G]CTTTTATGTTTATAA | 55632 |
rs530042581 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30585084 | TGTGATCTGCCCGCC[G/T]GGGCCTCCCAAAGTG | 55632 |
rs530068607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30596010 | GATACTTCCTTTTAT[C/T]GTATACCATATTTAG | 55632 |
rs530108900 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30587081 | CTAAGTGAAAAAAGG[-/A]AAAAATGATTAGGTC | 55632 |
rs530132811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30596760 | TGTCATGTTTTTTGG[C/T]ACATAATACCAAATG | 55632 |
rs530253220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30590860 | GGTTTGGAACTACAG[A/G]TTGAATATCCCTTAT | 55632 |
rs530292551 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30574508 | GGTTTGTTGCACATA[C/T]TATTTCATCACCCAG | 55632 |
rs530298008 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30577261 | AAAAGAAAAAATGTT[G/T]GGTGGTTAGGATCTG | 55632 |
rs530317074 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30583679 | ACCACAAGTGGTAAA[C/T]ATGTGAAGTAATGCA | 55632 |
rs530356999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30569659 | GATTGGGCTGGTTAT[C/T]TAGAGCCTGACTTGG | 55632 |
rs530363017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30613546 | TTTAGCCTAAGGAAC[C/T]TTTGTTATTTTTAAT | 55632 |
rs530394504 | snp | A/G | 0.00181241 | 0.0300487 | intron-variant | G2E3 | GRCh38.p7 | 14:30614242 | TGATAACAGATAAAC[A/G]TGTGTGTTCTTAGCT | 55632 |
rs530407658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30563881 | CTGCCACCACGCCCG[A/G]CTAATTTTTGTGATT | 55632 |
rs530548831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30607342 | CATAAAGTATACTTA[C/T]GCAAACCTAGTTGGT | 55632 |
rs530560028 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30596663 | TCTTTCATGTGTATA[C/T]TTAAAATACTCACAT | 55632 |
rs530564122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30592122 | TTATCGAAATTGTTA[C/T]AGGAGTGAATCTTTG | 55632 |
rs530626246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30585137 | CTGTACCCAGACAAT[A/G]GTGTCCTTTGAGTCA | 55632 |
rs530630020 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30561607 | GCATATTTAGCCATT[-/G]GCCTTTTTATTTCCC | 55632 |
rs530634088 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30591019 | GCATCATGTTGGCAC[A/T]CAGAAAGTTTCCTAT | 55632 |
rs530690378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30585681 | CTCTATTGTTTTTCC[A/G]TTCTCTATTTTGATT | 55632 |
rs530691287 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30579086 | GCAGTTCTGTAGTTA[C/T]TGTTTGAGAATGTAT | 55632 |
rs530882549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30583750 | ATATATCAAAACATC[A/G]TGCTAAACATTGTAA | 55632 |
rs530942405 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30601672 | TTGGGCGGGTGTGTG[C/T]GTGTTTGTGTGTAAG | 55632 |
rs531004376 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30569745 | CCAGCTGGTGAAGGG[C/G]GGGGATTATATTACT | 55632 |
rs531068101 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30570259 | AGATTCTTTGTCTTT[G/T]TTTTTGTCAGTTTGA | 55632 |
rs531068697 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30584150 | TGTGTGTGTTTGACT[A/T]CTTTCACTTAACATA | 55632 |
rs531099337 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30583513 | GTGCTGGTTACCAGC[A/G]GTTGGGAGGATTGGG | 55632 |
rs531205048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30575576 | GAAGAGAGGAAGTCA[A/G]ACTATCTCTTTGCAG | 55632 |
rs531272431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30615153 | TGGATTTGAAAGTAT[C/T]ATGTGTAGTATATCC | 55632 |
rs531402937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30576212 | AGCCCAGAAATGAGG[C/T]CACACATCTACAACC | 55632 |
rs531455568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30561205 | ATCTTTACAATATCG[C/T]TGAGGTAGTTACTAT | 55632 |
rs531572767 | snp | A/G | | | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558987 | TAGGGAGAGAGACCC[A/G]ACAAAACAAACAAGC | 55632 |
rs531573144 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30568097 | ATTTTGGGGCTCTTA[C/T]TAGGTGGGTTTGTGT | 55632 |
rs531588252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30567024 | CTTTGCATTTCTGGG[A/G]TAAATCCCACTTGGT | 55632 |
rs531622769 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30597182 | AATAAGATTGAAAAA[A/T]ATATATGGGTGATGT | 55632 |
rs531662307 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30560248 | GAACTTTAAATGTGT[A/G]CAAGTTTTACATCTT | 55632 |
rs531672252 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30609677 | GTCTTGCTAGCACAT[C/T]GAGTCTAACATGTTT | 55632 |
rs531677455 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30618964 | TTTTAAGGCTGTTTT[C/T]TCTTGCTCTTAATGT | 55632 |
rs531684371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30597721 | ATAAATGTCTCATTC[A/G]TTGATTTATAATCTC | 55632 |
rs531758918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30571644 | CGCCCAAAGCATTCA[A/G]TTATTTCAATACTAT | 55632 |
rs531764716 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30604618 | CTGGTCTGGGAGCAC[A/C]CTTTGTGACTTACTG | 55632 |
rs531798195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30588296 | AGTAAAATAAAAAGT[A/G]TTATTTTACTTTTTA | 55632 |
rs531800210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30595767 | TTATCCAATCTAGAT[A/G]GCTGTATGTGGTTAA | 55632 |
rs531912575 | snp | C/G | | | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558735 | AGAGGCCCAGGAAAG[C/G]CTGCACTAAGTACTT | 55632 |
rs531935877 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30611478 | CATCTGTACCTTTAA[C/G]AGCTAACCTGTATGA | 55632 |
rs531947226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30582370 | ATATAAAAATAATCT[A/G]CTTATAAAAATGCAT | 55632 |
rs531972633 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30611713 | CCCAGGCTGGAGTAC[A/G]TTGGTGTGATCATAG | 55632 |
rs532000677 | in-del | -/TAAAC | | | utr-variant-3-prime, downstream-variant-500B | G2E3 | GRCh38.p7 | 14:30619853 | GGTAAACTGCCTATT[-/TAAAC]TAAGTAATTTTTTGG | 55632 |
rs532005585 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30581842 | ATAAACAGTATCTGT[A/T]GTCTTGCTACAATGA | 55632 |
rs532069217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30605036 | TGAGTAGCTGGGATT[A/G]CAGGCATACGCCACG | 55632 |
rs532193251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30606255 | TTTTTTTTTTGCACA[A/G]TTATGTATATGATGG | 55632 |
rs532207522 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30562047 | TTTAAAATGCTTTAT[A/G]CATATTTTCTCACTT | 55632 |
rs532226249 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30597822 | TATAAATTAAGAGAA[A/T]CAAGATGTGATTTAA | 55632 |
rs532259981 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | G2E3 | GRCh38.p7 | 14:30620160 | CTAATAAAACAAATA[C/T]CTTATTCAGTCTCAG | 55632 |
rs532266940 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30562632 | AGTTTAGAGAAGACT[C/G]TACTCCTCCACCTCT | 55632 |
rs532284500 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | G2E3 | GRCh38.p7 | 14:30591107 | TTTCTTAAAACATCC[A/G]AATCCTCTCCAAGTA | 55632 |
rs532361602 | in-del | -/ACTT | 0.00199481 | 0.0315187 | intron-variant | G2E3 | GRCh38.p7 | 14:30562059 | TATACATATTTTCTC[-/ACTT]AATCCTCACAACCAT | 55632 |
rs532416326 | snp | A/G | 8.23771e-05 | 0.0064173 | intron-variant | G2E3 | GRCh38.p7 | 14:30598629 | TCAGTTGTGCTTAGT[A/G]GTTCCTTGTTTAAAC | 55632 |
rs532429916 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30559715 | GGTTTAGAATGAAAA[G/T]ATGCTCTACGTGGCT | 55632 |
rs532482719 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30595890 | CTTTCCACTCTGTGT[C/G]TACAGAATTGTCACT | 55632 |
rs532495068 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30573807 | CACCAGTAAACTGAG[G/T]AAAGTTTACCAATCT | 55632 |
rs532515876 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30589228 | TGTAAGTAGCCTCTT[A/T]CTTTGACCATGAAAA | 55632 |
rs532575645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30582390 | TAAAAATGCATGCCT[A/G]AAACCTAGTCTGTTC | 55632 |
rs532651023 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30583973 | AGTTCTAAAACATTT[A/T]AATCGCCCTCAAAGG | 55632 |
rs532804914 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30590096 | GCTGTATGCAGGGAA[A/G]CGTCTCCATATTGTC | 55632 |
rs532815310 | snp | C/T | | | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558924 | CCCCTCAAGAGCAAA[C/T]AGGCGGAAACAATGA | 55632 |
rs532895303 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30562379 | ATAACCTAGGAAAAA[A/C]CAGGCCATACAGAGA | 55632 |
rs532964371 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30587564 | GAGCTGGATAGTTCA[G/T]GCTCAGAGTCTCATG | 55632 |
rs532967101 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30617422 | TTGTTGTTGTTGTTT[G/T]TATCCTATGTTTGGT | 55632 |
rs532982997 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30574186 | TGCATATATCTGGTC[A/C]CCCTACCCCTTAATG | 55632 |
rs532987440 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30608323 | GTCTGTGTTCACCAT[G/T]GCTTGTGAATACTCC | 55632 |
rs533084408 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30573621 | GGTATAGGTTCCAGT[C/G]CGGATCTGAAGGCCT | 55632 |
rs533090629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30608815 | GGCAGTGTTGTTTAA[C/T]GATTAAAAGCATAGG | 55632 |
rs533092053 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30581656 | GCAGTGAGCAGAGAT[C/T]GCACCACTACACTTC | 55632 |
rs533122666 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30600292 | CATTCCTGATTCCCT[A/G]CTCTGGGCTAGGGGT | 55632 |
rs533288796 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30582492 | CACAGCATACAGCAG[A/G]TGTACCTCCATCCAG | 55632 |
rs533305610 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30575179 | TCTAATGATTAGTGA[A/T]GTTGAGCTTTTTTTC | 55632 |
rs533371127 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30610710 | TTAGGCTAAACTTCT[A/G]TATCTCATAGACCCA | 55632 |
rs533435890 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30619078 | CCAATATGGAAACTT[C/T]AACACCTTTTATACA | 55632 |
rs533442439 | snp | A/G | 3.33e-05 | 0.00408031 | synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30602126 | CCAGAGTAAAGATCT[A/G]CTGAGGTATGTATTT | 55632 |
rs533481496 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30610135 | TCTACTCCAGTTTCT[A/G]TACTTTTTATCCAGT | 55632 |
rs533487001 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558172 | CCGCCTCGGCCTACC[A/G]AAGTGCTGGGATTAC | 55632 |
rs533497537 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30618344 | TTTTTATTCCAAATA[C/T]GTTGATAAAAAGATA | 55632 |
rs533501415 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | G2E3 | GRCh38.p7 | 14:30594506 | CATCCTGGCTAACAC[A/G]GTGAAACCCCGTCTC | 55632 |
rs533549966 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558930 | AAGAGCAAATAGGCG[A/G]AAACAATGACCCCGC | 55632 |
rs533559217 | snp | A/C | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30576537 | GATCTAGTTAAACTT[A/C]AGGGTTTCTGCACAG | 55632 |
rs533586582 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30611983 | TTATAAATAGTTTCA[C/T]GTAGTAAAGTGGCAT | 55632 |
rs533593357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30601572 | ATTCTTTGTATGTGC[A/G]TATGAGTGTGATAAG | 55632 |
rs533648221 | snp | C/T | 1.72928e-05 | 0.00294043 | intron-variant | G2E3 | GRCh38.p7 | 14:30593665 | TATTTTGTAAGCTTT[C/T]TCTGATTGATATAAA | 55632 |
rs533677623 | snp | C/T | 0 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30559929 | TATTTAAACCGGCTG[C/T]GGTAACAGCGGTGGT | 55632 |
rs533715996 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30587033 | ATTTCGTGTTTGTTT[A/G]TTTGTTTGTTTTTCT | 55632 |
rs533770337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30573762 | CTAATGTCTACCCAC[A/G]CTGGGGATGGCCATC | 55632 |
rs533788008 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30566048 | TAATGGTCTTGGCAC[C/T]CTTATTGAAAATTAG | 55632 |
rs533870698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30608487 | AGTTAGAATACTTTT[C/T]CTTCCTTCTATAGGG | 55632 |
rs533895886 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30560567 | AGAGACATTGGCTAT[A/G]CTTCTCTAAGCCTTT | 55632 |
rs533980606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30560543 | TTTTTCATATAGTGT[C/T]TTTGTAACAGAGACA | 55632 |
rs534003338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30603327 | CGAGACTCTGTCTCA[A/G]AAAAAAAAAAAAAAG | 55632 |
rs534018023 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30594882 | GCCTGTAATCCCAGC[A/G]TTCTGGGAGGCCGAG | 55632 |
rs534019410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30601654 | CTTCCTTTAGTAAAT[C/T]GATTGGGCGGGTGTG | 55632 |
rs534084610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30593874 | TAATGTATATTTATA[C/T]TTAAAGAATTTTGTT | 55632 |
rs534096553 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30559973 | CTTAGTTTGCAAACA[A/G]TAGGGATAAGGTTTA | 55632 |
rs534172491 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558294 | GGTAATTCAATGTTA[C/T]TAGATGTGAGGATGA | 55632 |
rs534172549 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30602314 | TAAAGAAAATGAAAT[A/G]GGATAGAATAGAATA | 55632 |
rs534210817 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30607756 | TAAGATCTATATTTT[C/T]TACATAATGATAGCT | 55632 |
rs534291095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30593186 | TGAATACAATAATGT[A/G]TATACTGTATTGCTG | 55632 |
rs534334867 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | G2E3 | GRCh38.p7 | 14:30584867 | GGAGTCTTGCTCTGT[C/T]GCCCAGGCTGGAGTG | 55632 |
rs534339886 | snp | C/T | 0.000149131 | 0.00863385 | intron-variant | G2E3 | GRCh38.p7 | 14:30592278 | ATCATATTATAATAC[C/T]CAGATTTTTTATGTT | 55632 |
rs534353138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30586145 | GTGAAAGAAAGGCAA[A/G]CATCTGAGCTCATCC | 55632 |
rs534389326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30578611 | TCTAGGTTGGATGAC[A/G]GTGTAAATCTGTATT | 55632 |
rs534407674 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30580151 | CCTGTATAGAATCCT[C/G]GCAAATGCAACAGCC | 55632 |
rs534431705 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30585817 | ATTTTCTTTTTTAAC[A/T]TAGGCTTGCATGAGC | 55632 |
rs534449455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30579120 | CATCAAAAGCGCCAT[C/T]GTATACCTGTAGAGA | 55632 |
rs534457792 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30609276 | CATTGTCTCTACTTC[A/G]TATTTCCTATTTATT | 55632 |
rs534471141 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30580363 | AGGCATGCACCACCA[C/T]GCCCTGCTAACTTTG | 55632 |
rs534501251 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30578585 | ATTTAAATGCACTAC[A/G]TTTTGTGGTGTCTAG | 55632 |
rs534533178 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30617953 | ATTATGGGAAGTAAA[A/C]TGTTTTAACCATATT | 55632 |
rs534636337 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30564893 | GGTTGTTTCTTTGTA[A/G]TGTATTGATTTAGTG | 55632 |
rs534695792 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30607830 | TTTTAATATAAAAAA[G/T]GATGGTTATCTTATA | 55632 |
rs534705779 | snp | A/C/G | 3.32791e-05 | 0.00407905 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616410 | CTGTTGGAAACAAGT[A/C/G]TAATAACTGTTTAGC | 55632 |
rs534756940 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30562370 | TCTACAATCATAACC[C/T]AGGAAAAACCAGGCC | 55632 |
rs534808505 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30613719 | TTTTTTAAAATCAAA[A/C]TTTTTTTTAAAGATA | 55632 |
rs534817959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30571336 | TTGAGTTGTAAGCAT[C/T]CTTTATGCATTGTGG | 55632 |
rs534882748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30564407 | GCACAATCATAGTTC[A/G]CTGCAGCCTCCAACT | 55632 |
rs534944140 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30557580 | GATGTTTACAGCTTA[C/G]GTATCCATCCCAAAA | 55632 |
rs534995070 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30591382 | TCTATTTATGTACCA[C/G]TGTTACATTTCAGTT | 55632 |
rs535079008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30615781 | AGTTTAGGTGAAAGG[C/T]ATTCTTTCTAGAAAA | 55632 |
rs535081019 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30569832 | CAGCAAGAGCAACTT[C/G]CAGAAGAAATTCCTG | 55632 |
rs535115003 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30602207 | ATGCCATATACATTT[A/G]GAATATTAGGTGATC | 55632 |
rs535260801 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30606529 | TCCCTTTAAAATAAA[A/C]TGTAAAAATAAAGAA | 55632 |
rs535296675 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | G2E3 | GRCh38.p7 | 14:30564506 | CTGGCTAATTAAAAA[-/T]TTTTTTTTATAGAGA | 55632 |
rs535318887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30598960 | GGCTGCCATTAACAA[A/G]ATGCCACAGACTGGG | 55632 |
rs535358266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30600987 | AGCTGTTTCTTCCTC[C/T]GCACTGTTGTCACTG | 55632 |
rs535379688 | in-del | -/TAAGTATTAATTAGCTT | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30597203 | TGGGTGATGTAAAGC[-/TAAGTATTAATTAGCTT]TTTTTTTAACCATTG | 55632 |
rs535414046 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30559057 | GGAGCGCCAGAAGGG[C/G]GGGAGCACACGGGCC | 55632 |
rs535440597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30579234 | AGTTGTGGAGAGGAG[C/T]TAGGAAAAATAGTAC | 55632 |
rs535462285 | snp | C/G | 0.0023933 | 0.0345097 | utr-variant-3-prime, downstream-variant-500B | G2E3 | GRCh38.p7 | 14:30619524 | TCAAGTAATGCAATA[C/G]AAAGTTTCATGCTTC | 55632 |
rs535487402 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30562905 | CCTGTCCAGTGGACA[C/T]GTGACCCACGTGAAC | 55632 |
rs535663460 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30557144 | TTTAATTCCTGTGAA[A/G]GATAAGAATGGTGGG | 55632 |
rs535705278 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30614557 | CTCACCTCTTAAGGA[C/G]CCTATCTCCCATTGC | 55632 |
rs535738844 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30599755 | ATTTTGGAAATAAAA[A/C]TATATGTTATTTAAC | 55632 |
rs535774795 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30603002 | GAAAGTTTAAGGCAT[A/G]CATACTATTATCAAA | 55632 |
rs535807569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30605077 | TATTTTGTATTTTCA[A/G]TAGAGACAGGGTTTC | 55632 |
rs535853150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30570444 | CTGTTCCACTTTCTC[C/T]GGTCCCTCTTGGACT | 55632 |
rs535898623 | snp | C/T | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30575853 | ATTACAAAGCACTGC[C/T]CAAAGAAATCAGAGA | 55632 |
rs535908846 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30608580 | TAGGGATCGGGGAGG[A/T]CTTAATGCGTCCGCC | 55632 |
rs535942524 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30606601 | TATGGTGGAGAGTAC[A/G]TGAATTTAAATCACA | 55632 |
rs535951545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30590619 | CATTTATTCTTTTAG[C/T]TGAGGCAAAGAAGTG | 55632 |
rs535959660 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30587279 | GAAACCAGTTACTTT[A/G]TGTATCACTCAGAAG | 55632 |
rs536016573 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | G2E3 | GRCh38.p7 | 14:30599126 | AGTTGTCCCTCTGTC[A/G]GTGTGTTGTCTACGT | 55632 |
rs536080371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30599758 | TTGGAAATAAAAATA[C/T]ATGTTATTTAACTTT | 55632 |
rs536080467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30591844 | AACTTTTTGGAGACC[A/G]CTCTAAATCCACTGT | 55632 |
rs536205261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30588603 | ATGAACAGAAAAGTA[C/T]AGTGATGTTACAAAT | 55632 |
rs536260827 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | G2E3 | GRCh38.p7 | 14:30582040 | ATTTATGCTCCTAAA[C/T]CTCTTCTACTTTCTT | 55632 |
rs536301317 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30566077 | AGTTTACTATAAAAC[C/G]TGAGTTTATTTATTG | 55632 |
rs536326133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30574850 | TTTAGGCTGATTCCA[C/T]GTCTTTGCTATTGTG | 55632 |
rs536398613 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30591238 | AGTGACCTAGGTGGT[G/T]CTCAAAGGGGTCAGC | 55632 |
rs536452888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30567864 | TCCAGTTTTCCTTTT[A/G]TTGATTTCTAGTTTC | 55632 |
rs536453545 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30584290 | CATCCTTTGATGGAC[A/G]TTTGGCTTGTTTCTG | 55632 |
rs536461628 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30583886 | ATAAAATTCATACTT[G/T]AACTATTTTGAGATA | 55632 |
rs536511494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30561415 | GGCTTCTCATTGTCT[A/G]CCATATATAATTCAA | 55632 |
rs536591486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30569909 | ACACACTCTACTTAG[A/G]ATGCTTTTTCTGCCT | 55632 |
rs536663228 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30589324 | AGTATGGATATATAT[A/T]TTTTTAATGCCCAAC | 55632 |
rs536727120 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30582572 | GGACTCCTCTTTTGT[A/C]GACTCAGCTAATTCT | 55632 |
rs536764529 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | G2E3 | GRCh38.p7 | 14:30619870 | AACTAAGTAATTTTT[G/T]GGGATTTAATAAGAT | 55632 |
rs536794373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30577697 | GAGGAGGAAGTCACA[A/G]TGCCTTTTATGACAT | 55632 |
rs536946446 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30569933 | TCTGCCTTGTCTGCT[C/G]AGAATATTTATTTTT | 55632 |
rs536981962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30571177 | CTGTAGTGGGTTTGC[C/T]TTTTTTTTTTTGCTA | 55632 |
rs537007897 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30598219 | GCGAAACCCTGTCTC[C/T]ACTAAAAAATACAAA | 55632 |
rs537020687 | in-del | -/TTA | 0.0023933 | 0.0345097 | intron-variant | G2E3 | GRCh38.p7 | 14:30583263 | AACAGAAAAGATTAG[-/TTA]TTATACTAACATTTG | 55632 |
rs537042332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30614660 | GCACTCTAAAACTCA[C/T]GTCCCACTCACATAC | 55632 |
rs537079277 | in-del | -/TCTTC | | | intron-variant | G2E3 | GRCh38.p7 | 14:30615172 | TGTAGTATATCCATA[-/TCTTC]TCTTTTTCCTCACAT | 55632 |
rs537111806 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30613703 | AATCTATTTTGTTTT[G/T]TTTTTTAAAATCAAA | 55632 |
rs537181836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30568791 | TTTATATTTATTTTA[C/T]GTGTTTTTCTTTTAA | 55632 |
rs537243003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30562269 | AGTTATACTAGATAT[A/G]GATCTTAGATATGAT | 55632 |
rs537261943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30578583 | AAATTTAAATGCACT[A/G]CATTTTGTGGTGTCT | 55632 |
rs537306789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30562845 | CAGAAATAATGGTGT[A/G]AGCTGTCTCTCTCTC | 55632 |
rs537326788 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30570497 | ACTTGATGGTGTCTC[A/G]TAGTCTCTTGGGCTC | 55632 |
rs537342148 | snp | A/G | 0.00363017 | 0.0424489 | intron-variant | G2E3 | GRCh38.p7 | 14:30597397 | TAAATCATTAACAGT[A/G]GACTTTTTATTTTCC | 55632 |
rs537379120 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | G2E3 | GRCh38.p7 | 14:30563695 | GTAACTTTGTTACTT[G/T]TGTGTGTGTGTGTGT | 55632 |
rs537465683 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30583244 | TCTGTATAAATAAAC[A/G]TGTAACAGAAAAGAT | 55632 |
rs537522717 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30576575 | AACTACCAACAGAGT[A/G]AACAGACAACCTACA | 55632 |
rs537530129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30594999 | AAAAATTAGCTGGGC[A/G]TGGTGGTGCACACCT | 55632 |
rs537568395 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30567779 | GTATTTTCTAATTTC[C/T]CTTGTGATTTCTTTT | 55632 |
rs537643569 | in-del | -/TTTGTTT | 0.434109 | 0.169127 | intron-variant | G2E3 | GRCh38.p7 | 14:30565651 | GTTCAACTTCATTCC[-/TTTGTTT]TTTTTTTTTTTTTTT | 55632 |
rs537731981 | in-del | -/CTC | 0.00755907 | 0.0610114 | intron-variant | G2E3 | GRCh38.p7 | 14:30608335 | CATGGCTTGTGAATA[-/CTC]CTCAGAAATACATGG | 55632 |
rs537743852 | snp | A/C | 1.67083e-05 | 0.00289031 | missense, intron-variant | G2E3 | GRCh38.p7 | 14:30605737 | CAAGAATTTCTGAGT[A/C]TCTTAATGCAACATC | 55632 |
rs537795598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30582638 | TGCGGGTAAAAGTGT[A/G]GGTATTGGGGATGGA | 55632 |
rs537808417 | snp | A/G | 1.64871e-05 | 0.00287111 | synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30601833 | TTTAGCCTGCTCCTC[A/G]TTACGGTCATGGGAG | 55632 |
rs537820265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30584677 | TAATGGCTCTTTGTA[C/T]ATCTTCTTTGGAGAA | 55632 |
rs537837029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30567368 | TTGTTGAAATTTTCT[A/G]TTTCTTCTTGTCACT | 55632 |
rs537860607 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30618791 | ATTTTCTGCAGTGTC[A/G]TTTTGTCAAATGGTT | 55632 |
rs537871141 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30594063 | CAATGGTAAGCACTT[C/T]ACCATAACTTCTTAA | 55632 |
rs537934164 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30594652 | GAGCCAAGATGGCAC[C/T]ACTGCATTCCAGCCT | 55632 |
rs538003814 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30587751 | AAGGCTACTCGTGGC[A/T]TGGCATCTGGCTTCT | 55632 |
rs538034491 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30609043 | ACTCTTATAACTACT[A/G]TATGTTGTGTCACTT | 55632 |
rs538123241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30610794 | TCTAGATTTTAGGGT[A/G]AGAGTTGGCAAAAAA | 55632 |
rs538284451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30604362 | GACAGATTCATACTT[A/G]GTATGGAAAATGATC | 55632 |
rs538306053 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | G2E3 | GRCh38.p7 | 14:30619753 | CAGCCTATTTCCCCC[A/C]CTTTTAAAGACTGCC | 55632 |
rs538323565 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | G2E3 | GRCh38.p7 | 14:30587189 | GGGTTCAGGGAGTGG[A/C]ATAAAAGTATTTTAT | 55632 |
rs538385084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30580391 | TTGTATTTTTGGTAG[A/G]AACAGGGTTTCACCA | 55632 |
rs538560228 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30610397 | AGGTGGGTGGATCAC[C/G]GGGGTCAGCAGTTCG | 55632 |
rs538594650 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30603629 | GGAGGATCATTTGAA[C/T]CCTGGAGTTCGAAAC | 55632 |
rs538638760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30561391 | TGTTGCTCCATAAGT[A/G]TCTCTGATGGCTTCT | 55632 |
rs538665088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30587827 | GAACCATATGACCTA[A/G]TCATCACAGCCACAC | 55632 |
rs538727123 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30588409 | ACTTGTTTTTCTTTA[C/T]GATATACTGGTTAAA | 55632 |
rs538735772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30581003 | TGTCATTATGCATTG[A/G]CTGCAAGTAATAAAA | 55632 |
rs538775814 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30583587 | AATAAGTTCAAGAGA[A/T]CTGTTGTACAACATG | 55632 |
rs538789039 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30581870 | TGAAATATGAGGAAT[G/T]TAAATGATTACACTC | 55632 |
rs538793769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30589825 | TGCTGTTCTCTAAAC[C/T]TTTGATCCTGAGTCA | 55632 |
rs538823824 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30565480 | TTTTTTTCTTGTTGC[C/T]TGTGCTTTTGGTGTC | 55632 |
rs538854161 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30582772 | CTGAAATCTTTTAAA[A/G]GGTTAGGAGAGATAC | 55632 |
rs538936819 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | G2E3 | GRCh38.p7 | 14:30567430 | GTTAACTTTTAACTT[C/T]TTAGAGTACAATTGT | 55632 |
rs538980843 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30611543 | TGTTTATGCTGTTCA[C/G]TAAAATATTCTTGAT | 55632 |
rs539058321 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30603773 | TCATTTGAGCCCAGG[A/C]GTTCAAGCTGCAATG | 55632 |
rs539132714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30572703 | TTCTAAGATAAATCC[A/G]GTTAAGATATATTAT | 55632 |
rs539156435 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30590916 | AGATTTGAAATTTTT[A/T]TCAGATTTAGGAATA | 55632 |
rs539181682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30566009 | CCCAGGACCATTTGT[C/T]GAAGAGACTGTTTTC | 55632 |
rs539307425 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30559882 | TCTTTCACGGTTGAC[A/G]TTTTTCATGTACCGC | 55632 |
rs539322536 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30562514 | CAGCGTCTGGGAAGA[C/T]GCCCGTTGCCAAGAG | 55632 |
rs539345468 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30602812 | GATGGACATCTTGCT[A/G]TGTTGCCCAGACTGG | 55632 |
rs539355150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30567800 | GATTTCTTTTTTGAC[C/T]TTTTGTCTATTTAAA | 55632 |
rs539359718 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30581688 | GCCTAAGTGACAGAG[C/T]GAGACCCTGTATCAA | 55632 |
rs539380776 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30615721 | AAAAATAATGAGAAA[A/C]GATTACAGAGTAAAT | 55632 |
rs539430236 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30571962 | AAAAAAAAAAAACCT[C/G]CTGGGGATTTTGGTT | 55632 |
rs539601860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30600714 | CTCATCCTAGTGAGA[A/G]GAAGGCAGTTTTAGT | 55632 |
rs539617243 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30609811 | CTTCCAAGCTGTCTT[A/G]GAGAGTCATTTTCAT | 55632 |
rs539744560 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30572989 | AAAACATTGAAGATC[A/G]TATTGATGTTTTATG | 55632 |
rs539835971 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30617265 | CATCTCAAAAAAAAA[A/G]ACAGAATTGCACAAA | 55632 |
rs539901665 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30557364 | ATGAATGGACATAGA[C/T]TATCCAAACATTAGA | 55632 |
rs539911263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30609898 | TCAACCTTTCCTTCC[C/T]GTTTCTAGTGTGCCT | 55632 |
rs539943733 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30571198 | TTTTTTGCTATTTTA[A/G]TGTGCATTTCCTTTA | 55632 |
rs540034557 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30617709 | ATCCTTCTATAAACT[C/G]TTTACTTCTGTTTCC | 55632 |
rs540059164 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | G2E3 | GRCh38.p7 | 14:30585439 | CATTGAATGGTCTTG[A/G]CACTCTTGTTGAAAA | 55632 |
rs540098262 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616989 | GGTTAAATTTTGTTA[C/T]ATAAATCAGAGTCAT | 55632 |
rs540231294 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30609390 | CCAAAGGCCTTTTCT[A/G]ATTTTTCATCTGCTG | 55632 |
rs540266673 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30601214 | GCCCACACTTGTAGT[C/G]ATGGAGAAAATATGA | 55632 |
rs540275253 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30616096 | TTCTACTTTGAGATT[C/G]ATTTATGTACTGTTT | 55632 |
rs540289635 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30559197 | AATGTGGCTGCTCGC[G/T]GTCGGCGTGCCCCGA | 55632 |
rs540304002 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30604147 | ATGCAGTCATATTTA[G/T]AAGAATAGCATCAGC | 55632 |
rs540510206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30587952 | AACAAATTGTGGACA[C/T]ATTTTCAAATCTACC | 55632 |
rs540538395 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30593302 | CGAAGGTCCAGCTCT[C/T]TCCTTGGTCATAGAT | 55632 |
rs540586227 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30591986 | GCTTTCTCTTGAGAT[G/T]TCAATGAGGTGTTTA | 55632 |
rs540612637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30565385 | ACCCTTTTCAGGTTA[C/T]ATGATTTCTGAATAT | 55632 |
rs540643763 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30577969 | TTATTAAGACTTGGA[C/G]TGTTATTGAACTATA | 55632 |
rs540722218 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30578968 | ATGACTGGAAAAATA[C/T]GGATCTGTTTCTGAG | 55632 |
rs540875162 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30570860 | AGTTTTTTCAGAAAA[A/T]ATATTGTGGATCTAA | 55632 |
rs540902645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30564635 | CACCATGCCCAGTCA[A/G]AAATTAGCCATTTTA | 55632 |
rs540908326 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30572239 | TAAATATGTTGGTAG[G/T]ATTTTCTATGTAGAT | 55632 |
rs540953328 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30608707 | TTGCCAACATGTTAC[G/T]GCTTTAAAAACTGAG | 55632 |
rs541101041 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30570133 | CTTTCAGCACTTTAA[A/G]TATGTCATCTCACTG | 55632 |
rs541166951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30596536 | CCCCATCCTTGGAAT[A/G]TCTTTTGTCCTATTT | 55632 |
rs541215160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30614111 | AATATATTGAAAGTA[C/T]ATACAAAGAAGTATA | 55632 |
rs541232072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30590266 | TGAAGGACACTGACA[C/T]ATTATAGTTGAAGAA | 55632 |
rs541276249 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30597019 | CTGTCTTAGAGATTG[A/G]GTTAAAAACAGAACC | 55632 |
rs541427833 | snp | A/G | 0.000496243 | 0.015744 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30593494 | TTTGTTGGGACCATC[A/G]ACCTGTTCAAATAAT | 55632 |
rs541475716 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | G2E3 | GRCh38.p7 | 14:30604904 | TTCATTCATTCATTC[A/G]TTCATTTATGAGACG | 55632 |
rs541556416 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30564462 | CTCAGCTTCCCAGGC[A/G]GCTAGGACTACAGGC | 55632 |
rs541584759 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30595509 | GAGTTTTAATTTTGT[C/T]GTTAAAAAAGTAGAA | 55632 |
rs541596428 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30599430 | GATCGGGTTTCACCA[C/T]GTTGGTCAGCCTGGT | 55632 |
rs541608213 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30566099 | TATTTATTGACTCTT[C/T]CTTCTTTTCTATTGA | 55632 |
rs541652964 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30568109 | TTATTAGGTGGGTTT[A/G]TGTTTATAATTGTCA | 55632 |
rs541655188 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30557790 | GTAGACACAGATTAT[C/T]TTCTATCTTCCACTG | 55632 |
rs541878138 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | G2E3 | GRCh38.p7 | 14:30563876 | GGCACCTGCCACCAC[A/G]CCCGGCTAATTTTTG | 55632 |
rs541893422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30606161 | TATATTTGGAATTTG[C/T]GGTTAACATAGAGTT | 55632 |
rs541916937 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30607215 | GGATAAAGCATAAGT[A/C]AAACTTTTTATATTT | 55632 |
rs541987456 | snp | A/G | 1.65825e-05 | 0.00287941 | synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30607940 | GCTTGCCATTTCTTT[A/G]GTTCACGGTGGTCCT | 55632 |
rs542100341 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30578088 | TCAACTGAAATATGT[A/G]AATAGTACTTATTTT | 55632 |
rs542111021 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30567875 | TTTTATTGATTTCTA[C/G]TTTCATTCCATAGTC | 55632 |
rs542161060 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30570210 | TATTGGGGATATTTT[G/T]TATGTGTTAATCACT | 55632 |
rs542218878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30589050 | TAAGCTTAATTGTAG[A/G]TGTTCTTTCTTTCTT | 55632 |
rs542341966 | snp | A/G | 0.000134614 | 0.00820299 | intron-variant | G2E3 | GRCh38.p7 | 14:30598444 | CTCTTATGTAACATT[A/G]TTTATAGGTCAAAGC | 55632 |
rs542567314 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | G2E3 | GRCh38.p7 | 14:30573309 | AGTATTTCTTTTTGT[C/T]TCCAAATTTGTAGGA | 55632 |
rs542627490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30574122 | TATCATCCTGCAGTA[C/T]TGTACATTTGCATGT | 55632 |
rs542629908 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30590082 | ATAACAGCCACTATG[C/G]TGTATGCAGGGAAAC | 55632 |
rs542693149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30582858 | CTATTTCACTATATT[A/G]AATACGAGCTCATCT | 55632 |
rs542746877 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30589352 | AACTAGTTTCTTAGA[C/G]TTTATTTTCTAATTG | 55632 |
rs542797925 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30560177 | TCTAACCCAGTAGTA[A/C]AGTCATGCCTTCTGG | 55632 |
rs542853508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30576957 | TGGGGCCAGGCACGA[C/T]GGCTCACACCTGTAA | 55632 |
rs542940476 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30562533 | CGTTGCCAAGAGGAC[C/T]ATGGTCTAGCGATAG | 55632 |
rs543010343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30582924 | AGCCTATTAACAAAT[A/G]TAATACCTTTTAACA | 55632 |
rs543099765 | in-del | -/C | | | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558695 | GAAATAAATTAAAAG[-/C]CCTGACTGTGCCGGG | 55632 |
rs543148807 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30567471 | CTCATTTAATTCTTT[C/T]TATTTGTATTAGGTC | 55632 |
rs543209387 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30585992 | TTTTCCCAGTTTCTT[C/T]TTTCCTATGCCTTTC | 55632 |
rs543211507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30560800 | ATTCTGAATCAGTAG[A/G]TCTGGAGGATGGCAT | 55632 |
rs543214593 | in-del | -/CCTACAC | | | utr-variant-3-prime, downstream-variant-500B | G2E3 | GRCh38.p7 | 14:30619694 | AAACATATCCCAGTA[-/CCTACAC]CCTACACTATGCCAG | 55632 |
rs543294612 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30605341 | TATCAAATAACTGTT[A/T]TTGGTTCTAGTAGCA | 55632 |
rs543380382 | in-del | -/A | | | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30557465 | CAAAATTGCAAAATT[-/A]AAAAAAAAAGTTTAT | 55632 |
rs543423823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30567515 | CACTTTCATTTCTTC[C/T]GATTTAGTAATTTGA | 55632 |
rs543426832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30583561 | TACAAAATTTTATAA[C/T]AGACTGGTGGAATAA | 55632 |
rs543482604 | snp | C/G | | | utr-variant-3-prime | G2E3 | GRCh38.p7 | 14:30620059 | ATAAATTATTTAAGC[C/G]AAAAATCTGGACTCA | 55632 |
rs543485140 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30560888 | TGATTTGATCTTTCC[C/T]AGAAAGGCATTATAA | 55632 |
rs543529903 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30613184 | TACACATATGAAAGT[C/G]TGTAATCACCATCCA | 55632 |
rs543544320 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30561540 | TTCCAACCTGCTGAT[A/G]TTCTATCAATACTAC | 55632 |
rs543577188 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30595791 | TGGTTAAACAAATGT[A/C]ATTATTTGTAACCAC | 55632 |
rs543641887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30596389 | TTATTCTTCATACTA[C/T]TGTCTTTAACTTACC | 55632 |
rs543653963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30570040 | TCCCATGTGAGTATG[C/T]GTACTCATCTTCACT | 55632 |
rs543654055 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30562612 | AGTCTCCCTTTCCCC[A/G]GGGGAGTTTAGAGAA | 55632 |
rs543712312 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30562945 | ATTGGAGATGGCTCA[C/G]TGCCCCTTTGTCTTG | 55632 |
rs543860309 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30618093 | TATATCTCTTAATAC[C/T]AAAGGAAAACTAAAA | 55632 |
rs543919846 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30617363 | TACCTAAGAAAGTGT[A/G]TCTTCTTTAAAGCCT | 55632 |
rs543932430 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30564444 | CTCCAGCTGTCCTCC[C/T]ACCTCAGCTTCCCAG | 55632 |
rs543965483 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30604785 | TACATTTGCTTTTTT[A/T]AAAAAAGGACATAGT | 55632 |
rs544005661 | in-del | -/TAG | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30561908 | TAATTCTGTGTAGTT[-/TAG]TAGAGATTTTAGTGA | 55632 |
rs544007004 | in-del | -/C | 0.00358779 | 0.0422022 | intron-variant | G2E3 | GRCh38.p7 | 14:30589797 | CATCAGAATTATGAT[-/C]ATAACTCCACTCTGC | 55632 |
rs544042263 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | G2E3 | GRCh38.p7 | 14:30592529 | TGATATAATACTACA[A/G]TAAATTTTCTGTTTA | 55632 |
rs544095588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30581617 | CGAGGCAGGAGAATC[A/G]CTTGAACCCGGGAGG | 55632 |
rs544158192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30593241 | ATAATTATTAGTTTC[C/T]GAAATTCTGTATAAG | 55632 |
rs544201334 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30582001 | TAAAGTATCTTTTGA[C/T]ACCACATTATGTTGG | 55632 |
rs544274811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30611871 | TGCCCAGGATGTTCT[C/T]GAACTTCTGGCCTCA | 55632 |
rs544303939 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30586224 | AAGGTCCATTTTACC[C/G]CCTCTTGGACCAGTA | 55632 |
rs544321206 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30587405 | ATTAGTGGCACATTA[C/T]CACCTTAGCATGCCA | 55632 |
rs544367661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30580175 | AACAGCCACAAATAC[A/G]GTATAGACTAATAAA | 55632 |
rs544385201 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30605115 | GGGTCACACTGGTCT[C/T]GAACTCATGACCTCA | 55632 |
rs544544188 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30574939 | CCTCTGGCTATATAC[C/G]CAGTAATGAGATTGC | 55632 |
rs544619434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30579453 | ATATGAGCAAAACTA[C/T]GTTTAAATCCAAAAC | 55632 |
rs544788872 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30618242 | TCTTTGGCTTTGGTT[C/G]AATTTTTTTGTCTCA | 55632 |
rs544826132 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30572934 | CCCCTAGTACTCTTT[C/G]TACTATACCATGCTA | 55632 |
rs544827982 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | G2E3 | GRCh38.p7 | 14:30565661 | ATTCCTTTTTTTTTT[C/T]TTTTTTTTTTTTTTT | 55632 |
rs544860474 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558855 | TCATTCGCCCCATTC[C/G]TCGAAGGTGACGAAA | 55632 |
rs544887629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30575403 | GAGCCATCTATGACA[A/G]ACCCACAGCCAACAT | 55632 |
rs544890478 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30566120 | TTTCTATTGATGTGT[A/G]TGTCTGTCCTTGTGC | 55632 |
rs544957306 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30580204 | AAGGATTGTTTTTGT[G/T]TTTTTTTGTTGTTGT | 55632 |
rs544973821 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30585471 | CATTTGACCATAGAT[G/T]TATATATTTATTTCT | 55632 |
rs545005132 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30605033 | TCCTGAGTAGCTGGG[A/T]TTACAGGCATACGCC | 55632 |
rs545047995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30588178 | TGCAGTAAAAAGAAA[A/G]TCTTTCCATTTTTGT | 55632 |
rs545112402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30581687 | AGCCTAAGTGACAGA[A/G]CGAGACCCTGTATCA | 55632 |
rs545121063 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | G2E3 | GRCh38.p7 | 14:30620110 | TAGGTTAATGAACAA[C/T]CTGTAGCCATAGATT | 55632 |
rs545151461 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30619155 | TACAATTTTATACTT[C/T]GTAATTTTTAGTTTC | 55632 |
rs545179690 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30582184 | TACTTTTTCCTAAGA[G/T]GGACTGTTTCTTTAT | 55632 |
rs545196238 | snp | A/G | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30577152 | ATCACTTGAACCCAG[A/G]AGGCGGAGGTTGCAG | 55632 |
rs545365933 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30568903 | TGTTTTTATTTCCTC[A/G]TATGGCTTTGACTTA | 55632 |
rs545379656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30603044 | TCCCATGAGACAAAA[C/T]AGGCCGGGCATCGTG | 55632 |
rs545398836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30572345 | AGAGACTAAGGTGAA[C/T]GTTTGTAGATTCCCT | 55632 |
rs545405839 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30564571 | ACACCTAGCCTCAAG[C/T]GATCCTTCCACCTCA | 55632 |
rs545438379 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30565222 | GATTTACTTATCACT[A/G]ATATAATGAGCATTT | 55632 |
rs545467047 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30557896 | CTAGTAAACCTTTCA[A/C]ACTGTATTTTTTTTT | 55632 |
rs545617785 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30559382 | CCGGGGCCTCGCAGT[G/T]CTTTTGGGGACGTCT | 55632 |
rs545647169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30601125 | TGCCACTCACACACA[C/T]GGGGAGCTAAATCTG | 55632 |
rs545708497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30593343 | AATTTTTAGTGCCAA[A/G]GCTCCAGTCTGTTGT | 55632 |
rs545799817 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | G2E3 | GRCh38.p7 | 14:30615215 | ATGATTGTCTCTTGT[A/G]GGGGTTTTTTGGTTG | 55632 |
rs545907093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30599278 | TGTTGCCCAGACTGG[A/G]GTACAGTGGCATGAT | 55632 |
rs545923293 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30605325 | AATTTAAAACTAAGA[C/T]TATCAAATAACTGTT | 55632 |
rs546032585 | in-del | -/TTC | 0.00874735 | 0.0655527 | intron-variant | G2E3 | GRCh38.p7 | 14:30584937 | CCCAGGTTCAAGCAA[-/TTC]TTCTTCCTCAGCCTC | 55632 |
rs546127074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30563916 | TAGAGACAGGGTTTC[A/G]CCATGTTGGTCAGGC | 55632 |
rs546164819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30579266 | CTAGACCTACTTAAC[C/T]CTAAAGCCCCCTTAA | 55632 |
rs546178548 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30584027 | CACCCCTCATTTTCC[A/G]TGTCCCCAGCCCCTG | 55632 |
rs546311181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30591928 | TACAAATTGGTTTAT[A/G]GTATTTTCCTATTCT | 55632 |
rs546357699 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30567300 | CCCATCTGGGCTAGG[A/G]CTTTATTCGTTGGGA | 55632 |
rs546363109 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30587306 | GAAGAAAGCAAACGA[C/G]TGATTTCATACTCAG | 55632 |
rs546396191 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30569341 | GCATATAAGAACCCT[A/C]ATAGGTAGGTATTAT | 55632 |
rs546412595 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30580216 | TGTTTTTTTTTGTTG[G/T]TGTTTTTGAGATGGA | 55632 |
rs546478680 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | G2E3 | GRCh38.p7 | 14:30608163 | ATAATAGTATTATCT[A/G]TGAAGGAGTTAGGGA | 55632 |
rs546593281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30600553 | AATACATTCATAATA[C/T]TGATATTTTTCAAAT | 55632 |
rs546610682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30585206 | TTTTCTTTTGTTACC[C/T]GTGCTTTTAGTATCA | 55632 |
rs546624125 | in-del | -/TATTAA | 0.00517822 | 0.0506191 | intron-variant | G2E3 | GRCh38.p7 | 14:30615634 | TGTTTTGCCTTTTGG[-/TATTAA]TATTAAGATGCTAAC | 55632 |
rs546624189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30565908 | ACCTCATGATCTGTC[A/G]CCTCGGCCTCCCAAA | 55632 |
rs546657107 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30617613 | TCTGTTATATAAGCA[A/G]TGTATAAATAAAGTA | 55632 |
rs546741066 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30597913 | TTAAAATTAAAAATC[A/G]AAAGTGAAATATTTG | 55632 |
rs546752354 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30614525 | TCCATTTATGAGGGC[A/G]GAGCCCTTGTGACCT | 55632 |
rs546854811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30564937 | ATAGTGCTGCTGTGA[A/G]CATATGTATGCAAGT | 55632 |
rs546896240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30564010 | AGGCGTGAGCCACCG[C/T]GCCCAGCCATTGCTT | 55632 |
rs546938724 | in-del | -/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30575495 | CTCTCACCACTTCAA[-/C]CATAGTTTTGGGAGT | 55632 |
rs546981101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30584337 | AGTGCTGCTGTGAAC[A/G]TTAGTTTACAAGTAT | 55632 |
rs547047195 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30587237 | AAGAAACGTCTTGGC[C/T]AAAGGTGATAAATAT | 55632 |
rs547117049 | snp | G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | SCFD1, G2E3 | GRCh38.p7 | 14:30620437 | AAAATTGGGCTCTCA[G/T]ACATTTTATATTTCA | 55632 |
rs547125866 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30563565 | GACAGTGGAATCATG[A/C]AGAAACATGAAAATG | 55632 |
rs547155755 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30562661 | CTTGTGGAGGGCCTG[A/C]CACCAGTCAGGCCCA | 55632 |
rs547188230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30597203 | TGGGTGATGTAAAGC[C/T]AAGTATTAATTAGCT | 55632 |
rs547325054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30568556 | TTACCTTTTCTGCAC[A/G]TATTTTTTAGTTATA | 55632 |
rs547327356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30599590 | TGTACTAGGACTTAG[A/G]ATTTACTTCAACATA | 55632 |
rs547385725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30562196 | AGCCACCCAGGTGCC[A/G]AGGCAAGAGACTGGG | 55632 |
rs547414083 | snp | C/T | 0.000185995 | 0.00964172 | intron-variant | G2E3 | GRCh38.p7 | 14:30590714 | GGCACAAGGAAGAAC[C/T]GTGGGAGAAAGGTGA | 55632 |
rs547420970 | snp | C/T | | | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30559032 | CAGGTTAGCACCGAG[C/T]AGCAGCGCAGGAGCG | 55632 |
rs547451192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30595132 | GACAGAGCAAGATTC[C/T]GTCTTTAAAAAAAAT | 55632 |
rs547542321 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30597847 | ATTTAAAATATGTAA[G/T]AATTTTTTTAATACT | 55632 |
rs547549829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30582424 | ATTCAAGGCCCTCCA[C/T]ACTGGGTAGAGGGAG | 55632 |
rs547599519 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30574039 | CAGGAAAGTTGCAAG[A/G]AAAGTACAAAGAACT | 55632 |
rs547613455 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30617869 | AAAATTGGAAAACAA[A/C]GTCTGATGTCCTTAA | 55632 |
rs547635092 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30613413 | AGTTTATATGTCTTG[C/G]ACCAGTATAAGTCTC | 55632 |
rs547643463 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30608653 | CTAAACATGTCACAT[A/G]TGCAAACACTCATTT | 55632 |
rs547698006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30612459 | TAATGTGAGATATAT[C/T]TGGTAATAAGTGAGA | 55632 |
rs547787906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30604153 | TCATATTTAGAAGAA[C/T]AGCATCAGCATTCCC | 55632 |
rs547842881 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30562765 | CATGTTCCATCCTGT[A/G]CACCTGGCTCTGCCT | 55632 |
rs547862424 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30574218 | TTCAGTATTTCCTAA[A/G]AACAGTGATAGTCTA | 55632 |
rs547872328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30589237 | CCTCTTACTTTGACC[A/G]TGAAAAATAACTACT | 55632 |
rs547920823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30612664 | GGAGTTTGAGACCAG[C/T]CTGACCAACATGGTG | 55632 |
rs547922519 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30606313 | TTAAGGTAATTATAA[C/G]AGGCATCTCAAAACA | 55632 |
rs547953005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30591682 | TAAATCTCCCTCTCC[C/T]TTCTCTTGTAAAGAC | 55632 |
rs548013630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30592044 | CTTCAGTTTAAAATA[C/T]TTTAGTAGGAAGGAA | 55632 |
rs548150205 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30613654 | CTTTTCATTGAACCC[A/G]AATTAGAAAATCAAG | 55632 |
rs548151985 | snp | A/G | 0.000632722 | 0.0177753 | missense, intron-variant | G2E3 | GRCh38.p7 | 14:30605680 | GAAGTAGCATATGTT[A/G]TTGAAAATGATAATT | 55632 |
rs548182832 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30585128 | CATGAGCCACTGTAC[C/G]CAGACAATAGTGTCC | 55632 |
rs548258405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30589550 | TGGGAAGTCTTTTCT[A/G]TCAGTTTCTGTACTA | 55632 |
rs548264804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30606426 | TTTCATTTCATTTGA[A/G]TTTCCTACTATATTT | 55632 |
rs548398854 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30568756 | TTTACATTTATACAT[A/C]ATGTGCCCAATAACA | 55632 |
rs548404096 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30587369 | CCAATTTCTCACCTC[A/G]CTGAATTCATGCCTT | 55632 |
rs548455808 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30569676 | AGAGCCTGACTTGGT[C/T]AGTGGAAGGGGCTAG | 55632 |
rs548463382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30578499 | AACAAGAGGGACCAC[A/G]GGGCTTCTTACCAAA | 55632 |
rs548596542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30590309 | TTATCCCATAAATGC[C/T]GAAGTTGTTTAGACT | 55632 |
rs548616661 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | G2E3 | GRCh38.p7 | 14:30564627 | GTGTGAGCCACCATG[-/C]CCAGTCAAAAATTAG | 55632 |
rs548640329 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30598652 | GTTTAAACCTTCTGC[C/T]GAGAAAGTAGATTTT | 55632 |
rs548793032 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30579496 | CAGTATGAAATATAA[A/G]TTCTAATTGTAAGGA | 55632 |
rs548816076 | in-del | -/TC | 0.0193073 | 0.0963374 | intron-variant | G2E3 | GRCh38.p7 | 14:30573446 | GCGTGTGTGTGTGTC[-/TC]TGTGTGTGTAGAGAA | 55632 |
rs548851205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30560638 | AAAAATTGATCGCTA[C/T]ATCCTAATCTCTTTA | 55632 |
rs548877192 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30584777 | TTAATGCATCCTGGC[G/T]ACTAGACCTTTAGAT | 55632 |
rs548882194 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30608892 | GAGGCTGAGTCACAA[C/G]AATAATTTGAATCCG | 55632 |
rs548910053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30562790 | CTGCCTTTTAGATAG[C/T]GGTAGCAAATTAGGG | 55632 |
rs548956045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30573819 | GAGTAAAGTTTACCA[A/G]TCTTTTCCAGAAACA | 55632 |
rs549011892 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30601669 | CGATTGGGCGGGTGT[G/T]TGCGTGTTTGTGTGT | 55632 |
rs549075276 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30602274 | GACCCAACATTTGAT[A/C]ATGAAATCAATGCAA | 55632 |
rs549082773 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30575419 | ACCCACAGCCAACAT[A/T]ATACTGAATGGGCAA | 55632 |
rs549146171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30567638 | AAAAATTTTTTTATT[A/G]CATTATCTGGACTCT | 55632 |
rs549180984 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30603363 | AAAATAATAAGTTAC[A/T]TTCAAAATCTTAAAC | 55632 |
rs549189120 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30600657 | TCTTTCCAGGACAAA[C/G]ATATTGTCTATCTGA | 55632 |
rs549244456 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30604304 | AGAAAAAAGAAAAAG[C/G]AAAACCTGGCCTACA | 55632 |
rs549275816 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30583074 | ACAGTCCAGTGTGCA[C/T]GGTTTAAGGAAGATG | 55632 |
rs549307380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30596122 | TATATGGGTGGGTGG[A/G]TGGGTGGGTGTGCGT | 55632 |
rs549307388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30604918 | CATTCATTTATGAGA[C/T]GGAGTTTCGCTCTTG | 55632 |
rs549464554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30593933 | CACAATGAATAAACT[A/G]GATTTTAATTCCTAA | 55632 |
rs549623278 | in-del | -/A | | | intron-variant | G2E3 | GRCh38.p7 | 14:30593877 | TGTATATTTATACTT[-/A]AAGAATTTTGTTGTT | 55632 |
rs549626880 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30604320 | AAAACCTGGCCTACA[C/G]TAGGGCACTGTAACG | 55632 |
rs549629782 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30580407 | AACAGGGTTTCACCA[C/T]GTTAGCCAGGCTGGT | 55632 |
rs549698837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30581336 | TATAAGATATGGTTC[A/G]TATCTCAATAAAACA | 55632 |
rs549757849 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30617576 | AGCATTATACAGTTA[A/T]CTTCATTGCTCTTGA | 55632 |
rs549766920 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30601061 | CACCCACACAGAGGG[A/C]TGATATGCCCCCACC | 55632 |
rs549773872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30560251 | CTTTAAATGTGTACA[A/G]GTTTTACATCTTTAT | 55632 |
rs549792710 | in-del | -/A | 0.0349287 | 0.127453 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30576837 | AAAAATGCTAGATTA[-/A]AAAAAATCAATCAAT | 55632 |
rs549804624 | snp | A/T | 0 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30594718 | AGATGTAAATTCTCT[A/T]ATTTCAATAAAGTCT | 55632 |
rs549811366 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30597753 | TTATAAGTAGCTCAG[C/T]TATGTCCAATTTTAA | 55632 |
rs549818871 | in-del | -/TT | 0.029116 | 0.117091 | intron-variant | G2E3 | GRCh38.p7 | 14:30561848 | TCAAAAAGTTGTTGC[-/TT]TTTTTTTTTTTTAAG | 55632 |
rs549849326 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30583438 | GTCATGGAAAGACAA[G/T]ACTGCATAATCTCCC | 55632 |
rs549868232 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30595066 | TCGCTTGAACCCGGG[A/C]GGTAGAGGTTGCGGT | 55632 |
rs549877756 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | G2E3 | GRCh38.p7 | 14:30598392 | CTGCGTCTCAAGAAC[-/A]AAAAAAAGGTTTTTA | 55632 |
rs549886937 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30602604 | TATTTAATATAGAAA[A/T]TTTTTTTTCTTTTTT | 55632 |
rs549887944 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30568447 | GACATTTTAGTATTT[A/G]TTTTCTAAATACTAT | 55632 |
rs549924821 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30614064 | ATTATATAAAATGTT[C/T]TATATAGTTCCAAAG | 55632 |
rs549926510 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | G2E3 | GRCh38.p7 | 14:30604972 | CGTGATCTTGGCTCA[A/G]CGCAACCTCTGCTTC | 55632 |
rs549927660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30588350 | TTTATGTGTCTGCAG[A/G]TTATGTTTTCATAAC | 55632 |
rs549951295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30561932 | TTTTAGTGATAGCAT[A/G]TGGTTTATAAACTAT | 55632 |
rs549960589 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30565044 | TTAATGTGTTGTGGA[A/G]TTGCCAAACTGTTTT | 55632 |
rs549990868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30589151 | GTTACTTCCTGGAAT[A/G]CTTTTAGAAACTAAT | 55632 |
rs550068610 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30607316 | AGTAGGCAATTTCAT[C/T]ATGCAAAGATCATAA | 55632 |
rs550072127 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SCFD1, G2E3 | GRCh38.p7 | 14:30620405 | TTGCATTTGAAAGTG[C/G]AAGTACCCAAATGAG | 55632 |
rs550081304 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558782 | TCCTTCTTGCTGCTG[C/T]TGCTGTTTCCTCGAG | 55632 |
rs550104400 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30611744 | CTCACTGAACCTCCA[A/G]CTCCTGGGCTCAAAA | 55632 |
rs550105635 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30590409 | AAATGTCATTAGGCT[A/C]AAAGGTCCAAATTTT | 55632 |
rs550136832 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | G2E3 | GRCh38.p7 | 14:30581845 | AACAGTATCTGTTGT[C/G]TTGCTACAATGAAAT | 55632 |
rs550191108 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | G2E3 | GRCh38.p7 | 14:30603110 | AGGCGGGCGGATCCC[A/G]AGGTCAAGAGATCGA | 55632 |
rs550270637 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30568139 | ATGTCTTCTTGATGG[A/G]TTGAACTTTTTAGTC | 55632 |
rs550321192 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30572648 | TATTGTATTAACATG[G/T]TGTATTACTTTACTT | 55632 |
rs550384525 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30565948 | TACAGACGTGAGCCA[C/G]CACACCTGGCCAACT | 55632 |
rs550384567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30573532 | AGTGTGAACAGTCCC[A/G]TTATCTGTTTGCAAA | 55632 |
rs550422679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30608255 | AGTCAGATGGCTGGA[A/G]ATTAAAGTGCCACGT | 55632 |
rs550439653 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30582383 | CTACTTATAAAAATG[A/C]ATGCCTGAAACCTAG | 55632 |
rs550484066 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30616203 | GTCTATTTGGAGAAG[A/C]ATCTATGATGATAGC | 55632 |
rs550649712 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30559738 | ACGTGGCTCCGCGTT[C/G]CTCCTGAGAGAGATA | 55632 |
rs550708799 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30580853 | AGTGGTCATCTTAAT[A/T]GTTTTGACAGCTAAA | 55632 |
rs550714700 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30571629 | CTTCCCCCCACCCTC[C/T]GCCCAAAGCATTCAG | 55632 |
rs550722720 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30606866 | TTTAATTCAAGCTCT[G/T]ACAGTAAGGTAAGAC | 55632 |
rs550796735 | snp | C/T | 0.000157871 | 0.00888317 | intron-variant | G2E3 | GRCh38.p7 | 14:30615568 | TTATTTTACTTTTAA[C/T]GATCTCAGAATATTT | 55632 |
rs550810675 | in-del | -/CTT | | | intron-variant | G2E3 | GRCh38.p7 | 14:30609505 | CTTTAATGCTTCTTA[-/CTT]CTTCTTACCCCTGAA | 55632 |
rs550942893 | snp | A/C | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30575855 | TACAAAGCACTGCTC[A/C]AAGAAATCAGAGAAA | 55632 |
rs551019422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30571069 | ATTTTCTCCTCTGTG[C/T]TTTTTCTAGAAATTT | 55632 |
rs551101913 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30557219 | GTTTCTGCCTTCAAG[A/G]AACTTCAAGGAGCAA | 55632 |
rs551178845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30559890 | GGTTGACATTTTTCA[C/T]GTACCGCAAAAATCC | 55632 |
rs551211509 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30617429 | TGTTGTTTGTATCCT[A/G]TGTTTGGTATTCTGT | 55632 |
rs551301768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30593013 | TTGTTATCATGTAAG[A/G]AAACTACAGTTTAGA | 55632 |
rs551302227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30601435 | CACACTGACACAGCA[A/G]TCTCCCTGTAAGCAT | 55632 |
rs551359134 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30587623 | CTGAAGACTTTACTA[C/G]GTTGCAGGATCCATT | 55632 |
rs551360853 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30607584 | ACCACCTTAGTGTAT[C/T]TGGTCATTCTTGACC | 55632 |
rs551509498 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30574188 | CATATATCTGGTCCC[C/G]CTACCCCTTAATGCT | 55632 |
rs551627682 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | G2E3 | GRCh38.p7 | 14:30609511 | GCTTCTTACTTCTTC[-/T]TTACCCCTGAAACTT | 55632 |
rs551640006 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30612818 | GCTAAGATCATGCCA[C/G/T]TGCACTCCAGCCTGG | 55632 |
rs551660236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30601611 | GGTTTTTACATTAGA[A/G]ATATTTAGAGAAGCA | 55632 |
rs551712427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30603198 | GGGCATAGTGTTGTG[C/T]ATCTGTAGTCCCAGC | 55632 |
rs551841539 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30566982 | GTATGGTATATTATA[C/T]TGGTTGATTTCCATA | 55632 |
rs551849255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30610723 | CTGTATCTCATAGAC[C/T]CAGAAAGACAGTGGC | 55632 |
rs551857817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30592183 | TTTTTCAGGAAATTT[A/G]TTTAATATACCCTTA | 55632 |
rs551864945 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30619104 | ATACAATTCTCTACT[A/G]TTCAAGATATTCTTT | 55632 |
rs551866442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30607383 | ACACACCAAGGCTCT[A/G]TGGTAAAGCCTATTG | 55632 |
rs551867115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30600718 | TCCTAGTGAGAAGAA[A/G]GCAGTTTTAGTGAAA | 55632 |
rs551880558 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30565836 | CCGGCTAATTTTTTT[G/T]TATTTTTAGTAGAGA | 55632 |
rs551912539 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30591102 | CTTATTTTCTTAAAA[C/T]ATCCGAATCCTCTCC | 55632 |
rs551917498 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30609936 | CAAACTCAAATTTTC[C/G]CTAGGCTTAGACAAT | 55632 |
rs551920972 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30585138 | TGTACCCAGACAATA[G/T]TGTCCTTTGAGTCAC | 55632 |
rs551925871 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30599518 | AGGCATGAGCCACTG[C/T]GCTCGGCCATAATTA | 55632 |
rs551944055 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558938 | ATAGGCGGAAACAAT[A/G]ACCCCGCGCCCGGAG | 55632 |
rs551980603 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30618357 | TATGTTGATAAAAAG[A/G]TATTTGTTTCTTTAT | 55632 |
rs551984235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30585702 | TATTTTGATTATATC[C/T]ACTCTAATCTTTATT | 55632 |
rs551998543 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30563266 | TTTTTCCGTTTGATC[A/T]CTTAAGACAGTTGCC | 55632 |
rs552053322 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | G2E3 | GRCh38.p7 | 14:30594513 | GCTAACACGGTGAAA[A/C]CCCGTCTCTACTAAA | 55632 |
rs552175563 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | G2E3 | GRCh38.p7 | 14:30579507 | ATAAATTCTAATTGT[A/C]AGGAAGCATTGTATA | 55632 |
rs552311342 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30613709 | TTTTGTTTTTTTTTT[A/T]AAAATCAAACTTTTT | 55632 |
rs552373298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30579114 | TATAAACATCAAAAG[C/T]GCCATCGTATACCTG | 55632 |
rs552410202 | in-del | -/T | 0.00438332 | 0.0466095 | intron-variant | G2E3 | GRCh38.p7 | 14:30573201 | TTCATGAAAAAAAAA[-/T]TCTAATAGCTTTTGA | 55632 |
rs552447681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30578290 | ACTGCTATAATTTCA[A/G]GCTTAGAGAAAAGTT | 55632 |
rs552573189 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30583262 | TAACAGAAAAGATTA[C/G]TTATTATACTAACAT | 55632 |
rs552573410 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30590959 | TTGAGCACCTCTAAT[C/G]TGAAAATCCAAAACC | 55632 |
rs552581153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30578643 | TCGAATGACTAAAAC[A/G]TCCTTTATAAATTAA | 55632 |
rs552633766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30583762 | ATCGTGCTAAACATT[A/G]TAAGTATATACAGTT | 55632 |
rs552645059 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30579130 | GCCATCGTATACCTG[G/T]AGAGAATTACTAGTG | 55632 |
rs552646147 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30584269 | TATTTTGTTTATCCA[C/T]TTATCCATCCTTTGA | 55632 |
rs552650022 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30572073 | TCTCTCAGCAGTGTT[C/T]TGTAGCTTTTCAGAG | 55632 |
rs552669769 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30584933 | ACCTCCCAGGTTCAA[C/G]CAATTCTTCTTCCTC | 55632 |
rs552691486 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30569762 | GGGATTATATTACTT[A/C]CTATCTGATAATCCA | 55632 |
rs552706435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30571368 | TATAAATCCTTTGTC[A/G]GGTATATGTTTTGCC | 55632 |
rs552723569 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30601475 | TAAGTAGAAAGGAAA[A/T]TTTATTTTCTCCCTC | 55632 |
rs552826494 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30563805 | ACTCACTGCAACCTC[C/T]GCCTTCCCGGTTCCA | 55632 |
rs552830762 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | G2E3 | GRCh38.p7 | 14:30590111 | CGTCTCCATATTGTC[-/T]TAAGTAAAAATAATG | 55632 |
rs552913383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30564433 | CAACTCTTGGACTCC[A/G]GCTGTCCTCCCACCT | 55632 |
rs552928909 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30608555 | ATTTCTTCCAAAGGG[A/T]AACAAGTGGTAGGGA | 55632 |
rs552976400 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30557720 | GTGCCCGCAGCGTCA[A/G]TATATCAGATGCTAA | 55632 |
rs553113469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30569858 | TCCTGACATTCCCCA[A/G]ACATCCCAGGCTTTC | 55632 |
rs553197275 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | G2E3 | GRCh38.p7 | 14:30615815 | TATTGTCACCGCATA[C/G]AACAGTTTTAATCCT | 55632 |
rs553264092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30584012 | TACCTATTAAGTAGT[C/T]ACCCCTCATTTTCCG | 55632 |
rs553290527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30569093 | TGAGGTATAATATAT[A/G]TGCCAAATATATTTT | 55632 |
rs553337859 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30604391 | TCCATGGGCATTGCC[A/C]AAAACAAGATTATTT | 55632 |
rs553391156 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30610983 | TATCTGGCCCTTTAT[A/G]CAGATGGCCCTCTGT | 55632 |
rs553407920 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30586306 | GGGGAATGGTAGGTG[A/G]GTAAGTTAAGATGTT | 55632 |
rs553462965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30605258 | GATAATTATCTATCA[A/G]CTTTCTTGTACATGA | 55632 |
rs553473946 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30595702 | TCTAAAGGAGTTCCA[A/G]TAACTTTTGTACTCT | 55632 |
rs553483080 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30563900 | ATTTTTGTGATTTTA[G/T]TAGAGACAGGGTTTC | 55632 |
rs553484596 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30599269 | GTCTTGCTCTGTTGC[C/T]CAGACTGGAGTACAG | 55632 |
rs553526253 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30606142 | TTTGAATTCTTCCTG[C/T]TTGTATATTTGGAAT | 55632 |
rs553570341 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30570524 | GCTCTGTTTATTTTT[A/C]ATTTTTTTTCTTTCT | 55632 |
rs553576447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30591400 | TTACATTTCAGTTAG[C/T]GGCACTGGTAGTATA | 55632 |
rs553587756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30598399 | CTCAAGAACAAAAAA[A/G]GGTTTTTATTTTTAG | 55632 |
rs553651877 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30599105 | TTCTAGCTATGTCCT[C/T]ACACGAGTTGTCCCT | 55632 |
rs553658628 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30590562 | GGATGGAAAAATAAG[C/T]AGCTTTATTCAAGAA | 55632 |
rs553722745 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30587847 | CACAGCCACACACTA[A/T]TGTCACTTTTGCTTT | 55632 |
rs553758414 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30561393 | TTGCTCCATAAGTAT[C/T]TCTGATGGCTTCTCA | 55632 |
rs553778166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30596294 | TATTGTAATCCTACT[C/T]TCACTGCTTTAATTT | 55632 |
rs553941390 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30586897 | CTGATTTCTGAGAAT[A/T]GGATAAGTCATTTAA | 55632 |
rs554031615 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30566936 | TGCATCTATTGAGAT[A/G]AGCATGTGACCTTTT | 55632 |
rs554051632 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30611571 | GATAAAATTCTGTCC[A/G]TCTTTTAATTCTCAG | 55632 |
rs554142723 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | G2E3 | GRCh38.p7 | 14:30562594 | TAGCAGACCGGGAAA[A/G]GGAGTCTCCCTTTCC | 55632 |
rs554180433 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30591748 | GGATGATCTCAAGAT[C/T]CTTAACTTAATTACA | 55632 |
rs554246900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30590098 | TGTATGCAGGGAAAC[A/G]TCTCCATATTGTCTA | 55632 |
rs554251739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30591243 | CCTAGGTGGTGCTCA[A/G]AGGGGTCAGCAGTAA | 55632 |
rs554263158 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30619075 | TTTCCAATATGGAAA[C/T]TTTAACACCTTTTAT | 55632 |
rs554337085 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30610488 | AGGTGTGGTGGCGCG[C/T]GCCTATAGTCCCAGC | 55632 |
rs554378906 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30619182 | TTTCTGTAATTTGAG[C/G]AAGTGACTTTTTTTG | 55632 |
rs554418746 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30584536 | AGTCCTTTGTCAATA[C/T]TTGTTATTGTCAGAC | 55632 |
rs554438793 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30611053 | CTTGAGTTCCTTCCT[C/G]TCATTATCGTGTAAC | 55632 |
rs554439165 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30583902 | AACTATTTTGAGATA[G/T]ACAGTTTGGTGGCAT | 55632 |
rs554502654 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30577537 | CTTGATTGGGGCTGG[A/G]GGATTCACTTCTAAC | 55632 |
rs554597985 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30566096 | GTTTATTTATTGACT[C/T]TTTCTTCTTTTCTAT | 55632 |
rs554629092 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30564135 | TTTAGGGGTATAGTT[A/C]AATGAGTTTTAGTAA | 55632 |
rs554776440 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30576969 | CGATGGCTCACACCT[C/G]TAATCCCAGCACTTT | 55632 |
rs554914809 | snp | G/T | 0.00358779 | 0.0422022 | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30557868 | ATTACCTGTAGCATA[G/T]GTTCTCAGAAATCTA | 55632 |
rs554981852 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | G2E3 | GRCh38.p7 | 14:30605093 | TAGAGACAGGGTTTC[C/T]CCCTGTGGGTCACAC | 55632 |
rs554996986 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30567710 | TCTTTTTCTAGTTTC[C/T]TTGGGCATATAGTTG | 55632 |
rs555066293 | snp | A/G | 0.00795532 | 0.062565 | downstream-variant-500B | G2E3 | GRCh38.p7 | 14:30620113 | GTTAATGAACAATCT[A/G]TAGCCATAGATTATT | 55632 |
rs555168531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30561472 | AGAGCCCTTCAGAGT[C/T]TGGTACCAACTTCTC | 55632 |
rs555378880 | snp | A/G | 2.02419e-05 | 0.00318128 | intron-variant | G2E3 | GRCh38.p7 | 14:30615313 | ATACCAAACACACAT[A/G]TATGAATGTTGGCTC | 55632 |
rs555382481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30581594 | GTAATCCCAGCTACT[C/T]GCTAGGCCGAGGCAG | 55632 |
rs555424167 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30559956 | TGGTGATTAACTAGG[G/T]TCTTAGTTTGCAAAC | 55632 |
rs555459444 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30602067 | ATTACAGATTGTTTG[C/T]TGGAAGAGTCATCAC | 55632 |
rs555520312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30602899 | TTACAGGTGTGCGCC[A/G]CTATGCCCTGCCATT | 55632 |
rs555525220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30593224 | TACACAGGATTCTCA[A/G]CATAATTATTAGTTT | 55632 |
rs555583519 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30594895 | GCATTCTGGGAGGCC[A/G]AGGAGGGCGGATCAC | 55632 |
rs555644940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30595232 | AAAGGATCCTAGAGA[A/G]TGCAGTTAATAAACA | 55632 |
rs555774934 | snp | A/C/G | 0.00159649 | 0.0282165 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30618576 | AAAAACAGTATTTCA[A/C/G]TTCCTCATTTGACTT | 55632 |
rs555793277 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30591219 | GGGTTGGCAGGTATT[C/G]TCCAGTGACCTAGGT | 55632 |
rs555856560 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30611242 | CAGCTGAAACTCAGG[A/G]TTGAGGGTTTGCAGG | 55632 |
rs555970422 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30610124 | TCATGGCTTTATCTA[A/C]TCCAGTTTCTGTACT | 55632 |
rs556117611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30594103 | GATTACTGTCAATTA[A/G]TTAAAAATATTGGTT | 55632 |
rs556130192 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30618912 | ATAAATGTGTACATA[C/T]ATTTCTTAAATATTG | 55632 |
rs556172799 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30585065 | GGTCTCGAACTCCTG[A/T]CCTTGTGATCTGCCC | 55632 |
rs556177376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30603519 | AGTAGAAAATTAGTC[A/G]CTAAGCATGATGAAA | 55632 |
rs556242472 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30587796 | TGAGAGAGACAGAGA[G/T]AGAGAAATCAAGATG | 55632 |
rs556308330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30595382 | TAATTTTGTAGCAGT[A/G]TGTTATTTTTCATAA | 55632 |
rs556314474 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30578923 | GATTTTATTTTCCCT[C/T]GTTGAATTGCTTTGG | 55632 |
rs556371412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30588867 | TTACTGTCACATTGG[A/G]GGTTAAGGAAACTTT | 55632 |
rs556373125 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30596235 | TCCGTAAATCATTCC[C/G]CAAGTGTAATCAAGT | 55632 |
rs556440419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30589770 | ATGATCTGATGGTCA[A/G]TCTTCTCTGACCATC | 55632 |
rs556445076 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30572981 | ATGGTTAAAAAACAT[G/T]GAAGATCATATTGAT | 55632 |
rs556573144 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30599780 | TTTAACTTTTTTATA[A/T]TTTTTAATGTGGCTA | 55632 |
rs556627089 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30564463 | TCAGCTTCCCAGGCA[A/G]CTAGGACTACAGGCA | 55632 |
rs556649063 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30579251 | AGGAAAAATAGTACT[C/G]TAGACCTACTTAACT | 55632 |
rs556813048 | in-del | -/ATA | | | cds-indel, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30618074 | ATAGATTTGAAAGAG[-/ATA]ATATATCTCTTAATA | 55632 |
rs556825961 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30610798 | GATTTTAGGGTAAGA[C/G]TTGGCAAAAAATGGC | 55632 |
rs556902338 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558501 | TTTCAATAATCTCAC[A/G]GGACAATACTTAATA | 55632 |
rs556929359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30601025 | ACACACACATACACA[A/G]GACAGAAATTAACAT | 55632 |
rs556969264 | in-del | -/GTGA | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30584573 | ATTACAGCTATCCTT[-/GTGA]GTGTGAAGTGGTATC | 55632 |
rs557085322 | in-del | -/CTGT | 0.0103295 | 0.0711199 | intron-variant | G2E3 | GRCh38.p7 | 14:30565982 | TTCTTATTTACATGG[-/CTGT]CTGGTCGTCCCAGGA | 55632 |
rs557130890 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30606633 | AATCTGAATTCAAGT[C/T]TGTACACATCTAGTT | 55632 |
rs557184056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30608588 | GGGGAGGACTTAATG[C/T]GTCCGCCTAAAAATA | 55632 |
rs557254768 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30603257 | CTTGAACCCAGGAGG[C/T]GGAGGTTGCAGTCAG | 55632 |
rs557284898 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | G2E3 | GRCh38.p7 | 14:30562914 | TGGACACGTGACCCA[C/T]GTGAACTTACCTATC | 55632 |
rs557315175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30606182 | ACATAGAGTTTTTAT[A/G]ACATAGTTTCCTGGT | 55632 |
rs557320984 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30597333 | TTCATAATATATTGT[G/T]AAAAATAGCACATGT | 55632 |
rs557372056 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30609028 | TTACTTTGAATGCCA[A/C]CTCTTATAACTACTA | 55632 |
rs557374511 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30585350 | ATGGTGTGAGGTAGG[C/G]GTTCACCTATGTTCT | 55632 |
rs557392425 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30570777 | CTGTGTTTCTAGGGA[G/T]GTACAGGCCTGCAGA | 55632 |
rs557413923 | in-del | -/T | 0.290201 | 0.246747 | intron-variant | G2E3 | GRCh38.p7 | 14:30611820 | CACCCACACCAGGCC[-/T]TTTTTTTTTTTTCTT | 55632 |
rs557424677 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558668 | CTTTTTGTTTTCCCT[A/T]AACCCAGGACAGAAA | 55632 |
rs557484030 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30559143 | CTCTTTCCGGGTTTG[C/T]GAGCGGAAGTGGACG | 55632 |
rs557489327 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | G2E3 | GRCh38.p7 | 14:30572791 | TCTTGTGGCGTTTAT[A/G]TGTTGTTTCTAATTC | 55632 |
rs557499073 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30565273 | TTGAATATTTTCTTT[A/G]GAGAAATGTCTTCAG | 55632 |
rs557500714 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30607224 | ATAAGTCAAACTTTT[G/T]ATATTTATATACACA | 55632 |
rs557560649 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616895 | GGATTACATATAGAA[C/T]GCCACAATTTCTCTA | 55632 |
rs557567092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30591862 | CTAAATCCACTGTAG[A/G]TGTCTCAACACTTTT | 55632 |
rs557623958 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30615951 | AATCATTCTGCCTGA[G/T]AGAGTGGAGAAGAAT | 55632 |
rs557639133 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30587348 | CTTTGTTCCCCCTCC[A/C]CTCCACCAATTTCTC | 55632 |
rs557717102 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | G2E3 | GRCh38.p7 | 14:30594148 | TTACGTATCAAACCT[C/T]ATTACTACTTTTCAA | 55632 |
rs557718601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30607742 | TTTTATATTTTAGGT[A/G]AGATCTATATTTTCT | 55632 |
rs557764340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30572751 | AAAGAAAAACTACCA[A/G]TGATTGACTAAATTT | 55632 |
rs558033093 | snp | A/G | | | utr-variant-5-prime, missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30586748 | GAAAACATGATGACT[A/G]TCCTAATAAATACGG | 55632 |
rs558043271 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | G2E3 | GRCh38.p7 | 14:30594837 | TATTCAGTTAAAAGT[A/G]CAGGATGAAGGCAGG | 55632 |
rs558105432 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30591334 | TAGGTACTGTTCTGT[A/G]TTTTGCTAATGATTG | 55632 |
rs558118875 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30599318 | CTGCAACCTCTGCCT[A/C]CCGGGTTCAAGCAGT | 55632 |
rs558135736 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30564317 | TTGACCTTTTTTTGA[G/T]GTAAAATTCCCATTT | 55632 |
rs558168994 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | G2E3 | GRCh38.p7 | 14:30583954 | GAAACCATCACCACT[A/G]TCTAGTTCTAAAACA | 55632 |
rs558198861 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30557388 | CATTAGAAATTTATA[C/T]GCTCATTAAACCTGA | 55632 |
rs558230306 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | G2E3 | GRCh38.p7 | 14:30584851 | TTTTTTTTTTTGAGA[C/T]GGAGTCTTGCTCTGT | 55632 |
rs558306714 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30593123 | GGCGTAAGTTCCTGC[C/G]TCCCTTAATTTTATA | 55632 |
rs558359840 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30609224 | TTCGTTTTTCTTTTT[G/T]TGCCCTCTTTACTAA | 55632 |
rs558427138 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30617761 | TGCTACTAAAAGACA[A/G]TACCTAAAAGTAACT | 55632 |
rs558431005 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30579274 | ACTTAACTCTAAAGC[C/T]CCCTTAAAACTGGGC | 55632 |
rs558436445 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30578590 | AATGCACTACATTTT[G/T]TGGTGTCTAGGTTGG | 55632 |
rs558447119 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30588340 | GGAGAGCCATTTTAT[A/G]TGTCTGCAGGTTATG | 55632 |
rs558492125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30579995 | TAGAGAAAAGTTATA[C/T]TTCAGTAATGATTAT | 55632 |
rs558492355 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30617016 | TCATATATTCTGGGA[A/T]TTGTGTTACTATGCA | 55632 |
rs558501751 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30570540 | ATTTTTTTTCTTTCT[G/T]CTCTTCAGACTGGAT | 55632 |
rs558503422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30615727 | AATGAGAAAAGATTA[C/T]AGAGTAAATTTATAT | 55632 |
rs558554578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30567978 | TGGATATTGTTCCAC[A/G]TGCATTTGAGAAGAA | 55632 |
rs558566294 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30614878 | TAAAATTAATTTTCT[A/G]TCATATAAAATATCT | 55632 |
rs558655717 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30570776 | TCTGTGTTTCTAGGG[A/G]GGTACAGGCCTGCAG | 55632 |
rs558706921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30576585 | AGAGTAAACAGACAA[C/T]CTACAGAATAGGAGA | 55632 |
rs558758968 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30612851 | GACAGAGCAAGATTC[C/T]CTCTCAAAAAAATGA | 55632 |
rs558893207 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30577980 | TGGACTGTTATTGAA[C/G]TATACACTTAGATAT | 55632 |
rs558936923 | snp | C/T | 1.67674e-05 | 0.00289541 | missense, intron-variant | G2E3 | GRCh38.p7 | 14:30605744 | TTCTGAGTCTCTTAA[C/T]GCAACATCTTGAGAA | 55632 |
rs558948293 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30570392 | TCTTCCATGAAATTT[A/G]GGAAGTTTTTGGCTA | 55632 |
rs559001801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30598242 | AATACAAAAACCAGC[C/T]GGGCATGGTGGCAGG | 55632 |
rs559054257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30606279 | ATGATGGTTTTCTGT[C/T]TTCACTATTGGTGAG | 55632 |
rs559096141 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30605174 | GTGCTGGGATTACAG[G/T]TGTGAGCCACCGCGC | 55632 |
rs559117136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30607057 | AACATTATGTCTCAT[A/G]AAGTTAGAAATATCA | 55632 |
rs559160161 | in-del | -/CATT | | | intron-variant | G2E3 | GRCh38.p7 | 14:30604907 | ATTCATTCATTCATT[-/CATT]TATGAGACGGAGTTT | 55632 |
rs559205405 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30564454 | CCTCCCACCTCAGCT[C/T]CCCAGGCAGCTAGGA | 55632 |
rs559227209 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30595030 | GTGATCCCAGCTACT[A/T]AGGAGGCGGAGGCAG | 55632 |
rs559274776 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30569649 | GGGTACTTTGGATTG[A/G]GCTGGTTATTTAGAG | 55632 |
rs559325451 | in-del | -/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30592581 | ACATTATATGTATTA[-/C]CCTCCCGCCCACCCT | 55632 |
rs559435569 | in-del | -/T/TTTT | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30585649 | TTAAAAAGAACCAAC[-/T/TTTT]TTTTTTTTTTTACTC | 55632 |
rs559445570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30561687 | TTGCTTATAAATATA[C/T]AGTGCGAGACTGCCC | 55632 |
rs559557369 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30591647 | TCTTCACAGGCCTTT[A/C]TCTGTATATGCCTGT | 55632 |
rs559563595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30583652 | GAAAATTAGTAAATT[C/T]TAAGTATTCTCACCA | 55632 |
rs559612117 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30597639 | GACAGGTAGCCATTT[C/G]AAATGGTGAAATGCA | 55632 |
rs559663725 | in-del | -/AT | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30573407 | AACAGAAACAACAGG[-/AT]ATGTGTGTGTGTGTG | 55632 |
rs559715585 | in-del | -/AA | 0.00199481 | 0.0315187 | intron-variant | G2E3 | GRCh38.p7 | 14:30609163 | CTGTTTATTTGCCCT[-/AA]GACTGCTTATCCTAA | 55632 |
rs559819404 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | G2E3 | GRCh38.p7 | 14:30610475 | AAAAAAATTAGCCAG[A/G]TGTGGTGGCGCGCGC | 55632 |
rs560066805 | snp | C/T | | | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558433 | TTCAGAAGCTTAAGA[C/T]GTTTTGGATCAAAGA | 55632 |
rs560080198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30588192 | AATCTTTCCATTTTT[A/G]TAAGTTTATTTTACT | 55632 |
rs560101516 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30566145 | TTGTGCCAGTACCAC[A/C]TTGTCTTGATTACAG | 55632 |
rs560103802 | snp | C/T | | | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30557185 | GAATTATGAAAGACA[C/T]AGGAAAATATATAAC | 55632 |
rs560183858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30568063 | TCTCCTTTCATTTCT[A/G]TCAAATTTTGCCTTG | 55632 |
rs560239991 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30581744 | TAAAAGGAAAACTTA[A/C]CTCTACGTGCTCACA | 55632 |
rs560268037 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30600316 | TAGGGGTTCCCTTCA[C/T]TGTGCTTGTTACAAT | 55632 |
rs560296602 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30574295 | ATACAATACTTTCAA[A/C]TAAATATTGTTTTGG | 55632 |
rs560319533 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30565850 | TGTATTTTTAGTAGA[G/T]ACTGGGTTTCACCAT | 55632 |
rs560324824 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30618247 | GGCTTTGGTTGAATT[G/T]TTTTGTCTCACCAAT | 55632 |
rs560359852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30575411 | TATGACAAACCCACA[A/G]CCAACATTATACTGA | 55632 |
rs560373939 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30603057 | AATAGGCCGGGCATC[A/G]TGGCTCACGCCTGTA | 55632 |
rs560469786 | in-del | -/TG | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30577336 | TTGACTTACTTTTTT[-/TG]TGTTAGTTATCTGTT | 55632 |
rs560473767 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30604162 | GAAGAATAGCATCAG[C/G]ATTCCCCTGATCCAG | 55632 |
rs560510599 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616704 | TAGGCTAAAAAAAGG[-/T]TTTTTTTTGTTAAAG | 55632 |
rs560551193 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30582737 | AACAGTTCCCTTGTA[C/T]GGAAGGGAAGGAAGA | 55632 |
rs560582598 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30594519 | ACGGTGAAACCCCGT[C/G]TCTACTAAAAATACA | 55632 |
rs560598537 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30575406 | CCATCTATGACAAAC[C/T]CACAGCCAACATTAT | 55632 |
rs560625929 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30559404 | GGGACGTCTGGTGCT[C/G]GGGCCCGGCCTGGAG | 55632 |
rs560630988 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30566295 | AAAAGGCCATCGGGA[G/T]TTTGACAGGAATTGT | 55632 |
rs560686777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30560139 | AATTTTTAATGATGA[A/G]CTATCTGAAATATGG | 55632 |
rs560863386 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30594998 | AAAAAATTAGCTGGG[C/T]GTGGTGGTGCACACC | 55632 |
rs560918488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30582314 | GAAATCAGGACAATT[C/T]TACCAAATTTTAAAC | 55632 |
rs560920845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30574129 | CTGCAGTATTGTACA[C/T]TTGCATGTAACTTCC | 55632 |
rs560932349 | snp | C/T | | | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30557681 | TTTCATTTCAGTACC[C/T]GCTGATCTACTTCAT | 55632 |
rs560956033 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30568053 | CTAAACTATTTCTCC[A/T]TTCATTTCTGTCAAA | 55632 |
rs560967232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30576201 | ACAGAATACAGAGCC[C/T]AGAAATGAGGCCACA | 55632 |
rs561075681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30603103 | GAAACCTAGGCGGGC[A/G]GATCCCGAGGTCAAG | 55632 |
rs561099761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30566440 | TGTTTTGTAGTTTTC[A/G]GTGCAAAAATCTTGC | 55632 |
rs561137142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30595053 | GGAGGCAGGAGAATC[A/G]CTTGAACCCGGGAGG | 55632 |
rs561159262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30613096 | CCTGCTGTCCTTTAG[C/T]TTAGAACACTGGTCT | 55632 |
rs561161333 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30559639 | AGTAGTTAAATCTCA[C/T]TGTGAAGGCGTTGCC | 55632 |
rs561168050 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SCFD1, G2E3 | GRCh38.p7 | 14:30620363 | GGAGAGAATCTGTGA[G/T]GGAACTGAAGTGGCT | 55632 |
rs561170261 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30610596 | CAACAGAGTGAGACT[C/G]CATCCCAAATAAATA | 55632 |
rs561193597 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30597163 | AAGTAAAATGACATT[A/G]CACAATAAGATTGAA | 55632 |
rs561233221 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30618930 | TTCTTAAATATTGCA[A/G]TTGCCTAAATGTTGT | 55632 |
rs561378507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30588285 | TTTCTATAAAAAGTA[A/G]AATAAAAAGTATTAT | 55632 |
rs561432800 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | G2E3 | GRCh38.p7 | 14:30560205 | TGGAATGGTTTAAAA[A/G]TGTGCCATAAATGTA | 55632 |
rs561458555 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30561632 | TTTCCCCTTAAGATT[G/T]TACTCAAATGGGTTT | 55632 |
rs561537686 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30617451 | GTATTCTGTATGTCT[C/G]ATCCATAATCATTTT | 55632 |
rs561565981 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30589532 | ATAAATATTGTCAAT[A/T]CTTGGGAAGTCTTTT | 55632 |
rs561570831 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | G2E3 | GRCh38.p7 | 14:30619839 | TTTATGCCACTAAAG[A/G]TAAACTGCCTATTTA | 55632 |
rs561643008 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30574163 | TTCTGAACCGTTGGA[G/T]AGTAGGTTGCATATA | 55632 |
rs561645245 | snp | A/C | 0.000332817 | 0.0128956 | utr-variant-5-prime, missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30586790 | CTAAGGAGAAATGGA[A/C]TCTCACTGTACATTA | 55632 |
rs561657859 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30573409 | CAGAAACAACAGGAT[A/G]TGTGTGTGTGTGTGT | 55632 |
rs561758844 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30604473 | TGAGCTGGTTTATAT[C/T]GTCACTTGGATTGTT | 55632 |
rs561786626 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30594317 | GAACTTAAGTTTAAT[A/T]CTGTTTTTTAAAGTT | 55632 |
rs561807489 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30573730 | TTCTGGTTTTATTCA[C/G]GCCCTCAGTGGACTA | 55632 |
rs561846738 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30598012 | TAACTGTATGATAAA[A/G]TAACACTAATGGATT | 55632 |
rs561858567 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30609419 | TGTGACTTCTGCAAT[C/T]ACCACTTAGAATTTC | 55632 |
rs561892425 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30618265 | TTGTCTCACCAATAG[C/T]AATTGAAAGATCAAT | 55632 |
rs561905062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30587389 | ATTCATGCCTTAAGA[C/T]ATTAGTGGCACATTA | 55632 |
rs561917698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30585081 | CCTTGTGATCTGCCC[A/G]CCTGGGCCTCCCAAA | 55632 |
rs562050480 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | G2E3 | GRCh38.p7 | 14:30594903 | GGAGGCCGAGGAGGG[C/T]GGATCACCTGAGGTC | 55632 |
rs562111951 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30579033 | GTTTAAAATGATGTT[C/G]TATAGATTGTGATCC | 55632 |
rs562113194 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30577856 | GTAGAGGTAAGCAGT[A/G]GAGGACACTCAGAAT | 55632 |
rs562133410 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30566110 | TCTTTCTTCTTTTCT[A/G]TTGATGTGTATGTCT | 55632 |
rs562157608 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | G2E3 | GRCh38.p7 | 14:30585587 | TAATCTTCTCCCCCT[C/T]TTTTTTTTTGGTTAG | 55632 |
rs562175012 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30579369 | AGGAATAAACAAAAT[A/G]TTGAAAGCTTAGAGT | 55632 |
rs562179603 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30564638 | CATGCCCAGTCAAAA[A/C]TTAGCCATTTTAAAG | 55632 |
rs562243519 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30618156 | ATGTCTTTTTCAATC[G/T]GTACACTAACATACC | 55632 |
rs562303775 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30617366 | CTAAGAAAGTGTGTC[G/T]TCTTTAAAGCCTTGG | 55632 |
rs562397828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30600613 | ATTTCTTGTATACCA[C/T]TGGTCTCTCAATCAG | 55632 |
rs562405339 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30565423 | CATTCTGTAGATTGT[C/T]ATTAGATGCACAAGT | 55632 |
rs562442852 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30608780 | ACTTAAGCATATTCT[A/T]TCCATTGTCTCAATT | 55632 |
rs562455651 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30594468 | GCCGAGGAGGGTGGA[G/T]CACGAGGTCAGGAGA | 55632 |
rs562521437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30594923 | CACCTGAGGTCAGGA[A/G]TTCGAGACCAGCATG | 55632 |
rs562540045 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30609335 | CCAGTCTCAAGTTAG[C/G]TAGTTCATAGTTTAT | 55632 |
rs562612777 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30611890 | CTTCTGGCCTCAAGC[A/G]GGCCTCCCACCTCAG | 55632 |
rs562679732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30581645 | AGGCAGAAGTTGCAG[C/T]GAGCAGAGATCGCAC | 55632 |
rs562705987 | snp | C/T | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30576935 | AGGCACTTTAGAAAA[C/T]GTTGGATGGGGCCAG | 55632 |
rs562740986 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30601628 | TATTTAGAGAAGCAG[A/T]TAATCTTTTTCTTCC | 55632 |
rs562745387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30574176 | GAGAGTAGGTTGCAT[A/G]TATCTGGTCCCCCTA | 55632 |
rs562804253 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30603164 | AACCCCGTCTCTATT[A/T]AAAATACAAAAATTA | 55632 |
rs562835626 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | G2E3 | GRCh38.p7 | 14:30620056 | AGAATAAATTATTTA[A/G]GCCAAAAATCTGGAC | 55632 |
rs562910692 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30570814 | TGCTCCACCATTTTC[C/G/T]TGGATGTGTTCTGTA | 55632 |
rs562941722 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30596616 | ACCCTCTGACATAAT[C/T]ATCAGTATAGACTTA | 55632 |
rs562944541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30580191 | GTATAGACTAATAAA[A/G]GATTGTTTTTGTTTT | 55632 |
rs562966676 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558869 | CCTCGAAGGTGACGA[A/G]ACTTCAGCACATCTC | 55632 |
rs562999470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30572284 | ACAGTTTTACTTCAT[C/T]CTTCACAGTTTTGTC | 55632 |
rs563003729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30601470 | ATCTCTAAGTAGAAA[A/G]GAAAATTTATTTTCT | 55632 |
rs563035422 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30565790 | CCTCAGCCTCCCAAG[G/T]AGCTGGGACTATAGG | 55632 |
rs563052982 | in-del | -/ATC | | | intron-variant | G2E3 | GRCh38.p7 | 14:30593003 | ATTTAATGGATTGTT[-/ATC]ATGTAAGAAAACTAC | 55632 |
rs563133144 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30566392 | GCAAAATGTCTTTTC[A/G]TTTATTTACAGTTCT | 55632 |
rs563165034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30559292 | GTAAATGGGGAACGG[A/G]AAGACGCAGAACGTT | 55632 |
rs563222555 | snp | C/G | 1.66114e-05 | 0.00288192 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30602121 | GGATCCCAGAGTAAA[C/G]ATCTACTGAGGTATG | 55632 |
rs563258210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30614340 | AGTTCTGGAGGCTGG[A/G]AAGTCCAAAGGCATA | 55632 |
rs563296407 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30606385 | CTTTTGCTGTAATAG[A/G]AAATTTGAAAGAAAA | 55632 |
rs563331164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30568467 | CTAAATACTATCTTT[C/T]TGTTCCTCATTTCCT | 55632 |
rs563424029 | in-del | -/T | 0.34589 | 0.251098 | intron-variant | G2E3 | GRCh38.p7 | 14:30573007 | TGATGTTTTATGTAC[-/T]TTTTTTTTTGGATGG | 55632 |
rs563448126 | snp | C/T | 0 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30585676 | ACTCCCTCTATTGTT[C/T]TTCCATTCTCTATTT | 55632 |
rs563657378 | in-del | -/GAGAGAGACA | 0.00199481 | 0.0315187 | intron-variant | G2E3 | GRCh38.p7 | 14:30587782 | CCCAAAGCAAGTGAT[-/GAGAGAGACA]GAGAGAGAGAAATCA | 55632 |
rs563695046 | in-del | -/CT | | | intron-variant | G2E3 | GRCh38.p7 | 14:30571062 | CACAGAAATTTTCTC[-/CT]CTGTGTTTTTTCTAG | 55632 |
rs563707332 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30564583 | AAGCGATCCTTCCAC[C/T]TCAGCCTCCCAAAGT | 55632 |
rs563768906 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30557947 | AGACAGAGCCTCGCT[C/G]TGTCGCCCAGGCTGG | 55632 |
rs563854330 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30568956 | CTCTAGTAGGACAGA[G/T]CTACTAAAAGTTTCC | 55632 |
rs563926092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30585733 | TTTTTGTTTCTTCTG[C/T]TAGCTTTGGGTTTAG | 55632 |
rs563938918 | in-del | -/CACAAAAAC | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30576356 | CTTCCTAACACCATA[-/CACAAAAAC]CACCTCAAGATGGAT | 55632 |
rs563969482 | snp | G/T | 1.67298e-05 | 0.00289217 | intron-variant | G2E3 | GRCh38.p7 | 14:30597559 | TTATGATAAAAAAAA[G/T]ATATTTTAAATGTAG | 55632 |
rs563987859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30586613 | TATTATATGATTTGC[C/T]CTCAGAAAGAATTTA | 55632 |
rs564005163 | in-del | -/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30560112 | TTATTGTTTTGGGCT[-/T]TTTTTTTTTTTAATT | 55632 |
rs564010248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30578812 | GCATTTTATCTTCCT[A/G]TTATATTTTATCAAT | 55632 |
rs564048509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30592614 | TGGGGTCATTTCTAT[A/G]TGCCAAGTCTTGAGA | 55632 |
rs564051227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30580205 | AGGATTGTTTTTGTT[C/T]TTTTTTGTTGTTGTT | 55632 |
rs564098770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30615296 | AAATATTCCCTAATA[C/T]AATACCAAACACACA | 55632 |
rs564230216 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30601185 | CAACAAAAAGGCTGG[A/G]GCCCTACACTACAGC | 55632 |
rs564266159 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30597094 | GTAACTCAGGAGTTT[C/G]ATTTTTTTCTCACAT | 55632 |
rs564444111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30563921 | ACAGGGTTTCGCCAT[A/G]TTGGTCAGGCTTGTC | 55632 |
rs564500665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30578924 | ATTTTATTTTCCCTC[A/G]TTGAATTGCTTTGGT | 55632 |
rs564501294 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30575397 | TAATAAGAGCCATCT[A/G]TGACAAACCCACAGC | 55632 |
rs564518992 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30584227 | CCTTTTTATTGCTGA[A/T]TAATATTCCATCATA | 55632 |
rs564520896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30591932 | AATTGGTTTATAGTA[C/T]TTTCCTATTCTTCTT | 55632 |
rs564770364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30577071 | CTGTACTAAAAATAC[A/G]AAAATTAGCTAGGCG | 55632 |
rs564805504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30607431 | TGTATAACATGTTAC[C/T]GTACTGAATACTGTA | 55632 |
rs564806178 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30571576 | TTTTTTTCTTGTGAT[C/G]CAATTTGAATTAAGT | 55632 |
rs564832468 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | G2E3 | GRCh38.p7 | 14:30569386 | ACAAGGCAGAGCAAG[C/G]AGTTCAAACACAGAA | 55632 |
rs564876817 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30576336 | AGAAGATTGAAGCTG[A/G]ACCCCTTCCTAACAC | 55632 |
rs564902930 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30567517 | CTTTCATTTCTTCTG[A/G]TTTAGTAATTTGAGT | 55632 |
rs565009197 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30607423 | TGCAAACCTGTATAA[A/C]ATGTTACTGTACTGA | 55632 |
rs565039173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30562615 | CTCCCTTTCCCCGGG[A/G]GAGTTTAGAGAAGAC | 55632 |
rs565088265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30605344 | CAAATAACTGTTTTT[A/G]GTTCTAGTAGCAGCC | 55632 |
rs565100923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30613304 | ATATCATCTCAAACC[C/T]GATAAATTCATTTAA | 55632 |
rs565105519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30563105 | CTCTCGTCTCCGCAC[A/G]CGGGGAGAAAAACCC | 55632 |
rs565179121 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30611135 | AAAAGTGGAAGTTGA[C/G]AGCAGGGAAGTTTGA | 55632 |
rs565190860 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30590243 | TCATCATTACACTGG[A/C]GGGGAAATGAAGGAC | 55632 |
rs565251998 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30582956 | GTGACATCTATTCTT[C/G]ATTGCATGTATTATT | 55632 |
rs565261418 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30604794 | TTTTTTTAAAAAAGG[A/G]CATAGTAAATGTGAA | 55632 |
rs565341811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30605053 | AGGCATACGCCACGA[C/T]GCCCAGCTTATTTTG | 55632 |
rs565405624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30597220 | AGTATTAATTAGCTT[C/T]TTTTTTAACCATTGG | 55632 |
rs565405683 | snp | A/T | 3.73169e-05 | 0.00431938 | intron-variant | G2E3 | GRCh38.p7 | 14:30605476 | TACTTTAAAGTACTT[A/T]TCTCTATATTTAAAT | 55632 |
rs565497184 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30612462 | TGTGAGATATATTTG[A/G]TAATAAGTGAGATGT | 55632 |
rs565595789 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30589874 | TTATTCTTATACCTC[A/C]GTTTCTGAGATTGGA | 55632 |
rs565613510 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30584011 | GTACCTATTAAGTAG[G/T]CACCCCTCATTTTCC | 55632 |
rs565700063 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30613585 | GGTAATTCACAACCA[C/T]AGTCTGGATGCTAGA | 55632 |
rs565728560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30591236 | CCAGTGACCTAGGTG[A/G]TGCTCAAAGGGGTCA | 55632 |
rs565795020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30581999 | TTTAAAGTATCTTTT[A/G]ACACCACATTATGTT | 55632 |
rs565919894 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30575816 | CAGCTAACAAGGGAG[C/G]TGAAAGATCTCTACA | 55632 |
rs565986658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30584456 | AAGAACTGCTGGACT[A/G]TTTCCCAAAGCTCTA | 55632 |
rs566002449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30577456 | CTGCTTAGCTGTGTG[A/G]TTCTGGCTTAGGGTC | 55632 |
rs566007690 | in-del | -/AGT | 0.00597247 | 0.0543191 | intron-variant | G2E3 | GRCh38.p7 | 14:30597743 | TATAATCTCTTTATA[-/AGT]AGCTCAGCTATGTCC | 55632 |
rs566060349 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | G2E3 | GRCh38.p7 | 14:30588553 | AAAAAAAAGTACTGA[C/T]CCCAGACTTAACCCT | 55632 |
rs566217168 | in-del | -/GTGA | 0.0209421 | 0.100162 | intron-variant | G2E3 | GRCh38.p7 | 14:30563738 | TGTGTGTGTGTGTGT[-/GTGA]GATATAGAGTCTCAC | 55632 |
rs566255146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30568661 | CAGCTTTCATAGTAT[A/G]CAAAAATTACACTTC | 55632 |
rs566283083 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30574276 | TTCAGGAAACTTAGC[A/T]TAAATACAATACTTT | 55632 |
rs566330924 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30572785 | AGGTACTCTTGTGGC[A/G]TTTATGTGTTGTTTC | 55632 |
rs566359500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30608858 | GTGGTGGCATGTGCC[C/T]GTAATCCCAGCTACT | 55632 |
rs566361915 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30560530 | TAAAATATGAGCATT[G/T]TTCATATAGTGTCTT | 55632 |
rs566438859 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30607378 | CTACTACACACCAAG[A/G]CTCTATGGTAAAGCC | 55632 |
rs566456899 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30581261 | TATTGCATATATTTA[G/T]TTCAACAAAAACCTA | 55632 |
rs566511030 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | G2E3 | GRCh38.p7 | 14:30573734 | GGTTTTATTCAGGCC[C/T]TCAGTGGACTAGCTA | 55632 |
rs566518496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30567170 | TCTGGCTTTGGTATC[A/G]GGGTATTGGTGGCTT | 55632 |
rs566678553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30602858 | CTCAAGTAGTCCTCC[C/T]ACCTTTGCCTCCCAA | 55632 |
rs566742327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30603282 | AGTCAGCCAAGGTCG[C/T]GCCACTGTACTCCAG | 55632 |
rs566823717 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30578505 | AGGGACCACAGGGCT[G/T]CTTACCAAATGGAGT | 55632 |
rs566905789 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558194 | TGGGATTACAGGCGT[A/G]AGCCACCGCGCCCGG | 55632 |
rs566907233 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | G2E3 | GRCh38.p7 | 14:30619280 | CATTTGTAAATTTTT[C/T]CCCTAATTATATGGA | 55632 |
rs566964555 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30610750 | TGGCTCAAACAAGGC[A/C]GATGTTTACTGTTCT | 55632 |
rs566964850 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30559007 | AACAAACAAGCGAAG[A/G]CGACACAGCCAGGTT | 55632 |
rs567016771 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30610163 | AGTGTTTGTTCATTT[A/T]TTTAAGAAATACTAT | 55632 |
rs567027859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30610073 | TTGAACGAAGTTGAA[A/G]CTCTTCATTAGGGCA | 55632 |
rs567074442 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30618363 | GATAAAAAGATATTT[C/G]TTTCTTTATCCACCT | 55632 |
rs567190276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30580311 | TCCCGAGTTCAAGCA[A/G]TTCTCTTGCCTCAGC | 55632 |
rs567247066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30566712 | TTGCTTTATTATTCT[A/G]AATAGACCTTCTGGT | 55632 |
rs567354761 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30560651 | TATATCCTAATCTCT[G/T]TATTTTTTTCTACCT | 55632 |
rs567388294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30602326 | AATGGGATAGAATAG[A/G]ATACAAAATACCAAA | 55632 |
rs567390157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30593991 | ACCAGGATATTTGAA[A/G]TGATAAGAAGCTTGA | 55632 |
rs567408346 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30603407 | TGGAATTACATCTTT[A/T]TAATGTTGGGTATTT | 55632 |
rs567449796 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | G2E3 | GRCh38.p7 | 14:30594641 | GAGCTTGCACTGAGC[A/C]AAGATGGCACCACTG | 55632 |
rs567460084 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30564985 | TATTTCAATTGTTTT[C/G]GTTACATAGCTAGTG | 55632 |
rs567531500 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | G2E3 | GRCh38.p7 | 14:30596132 | GGTGGGTGGGTGGGT[A/G]TGCGTGTGTGTGTGT | 55632 |
rs567577014 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30589714 | TGACTTCACTTCCTT[A/C]TCTTATTCCAACATG | 55632 |
rs567626212 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30559053 | CGCAGGAGCGCCAGA[A/C]GGGCGGGAGCACACG | 55632 |
rs567685045 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30587183 | GTTTGAGGGTTCAGG[A/G]AGTGGAATAAAAGTA | 55632 |
rs567834683 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | G2E3 | GRCh38.p7 | 14:30580426 | AGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAG | 55632 |
rs567890683 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | G2E3 | GRCh38.p7 | 14:30571888 | TTAAAAATGTTTTTG[A/C]TATTACAAGACTTTT | 55632 |
rs567903992 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30581343 | TATGGTTCGTATCTC[A/C]ATAAAACAGTTATTT | 55632 |
rs567913327 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30618504 | AGTCACACACACATA[C/T]TTTGTTGGGGTGGGG | 55632 |
rs567954016 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30572587 | GTTGAATTTTGTCAA[A/T]TGCTCTTTCTGCATC | 55632 |
rs567955347 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30585261 | AAATCCAAAGTCACA[C/G]AGATTTACCCTTATT | 55632 |
rs567973552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30573850 | CTCTCACAGACACAT[C/T]CAAACATAAGTTTAA | 55632 |
rs567975861 | in-del | -/C | 0.00398564 | 0.0444627 | intron-variant | G2E3 | GRCh38.p7 | 14:30607342 | CATAAAGTATACTTA[-/C]GCAAACCTAGTTGGT | 55632 |
rs568041829 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30592845 | ATGTAAATTTGATTG[A/C]GTACACAAAGTAAAT | 55632 |
rs568160580 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30569615 | ACTGTAGTAAAAAAG[A/T]TGCCACCTGCTTTAA | 55632 |
rs568201658 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | G2E3 | GRCh38.p7 | 14:30565011 | TAGTGGAATTGCTGG[G/T]TGATATGGTAGTCTT | 55632 |
rs568205807 | snp | C/G | 0.000219667 | 0.0104778 | synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30615370 | GCAGGGTCTGAAAAC[C/G]CTTGGTGTTTTGGAG | 55632 |
rs568265009 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558448 | CGTTTTGGATCAAAG[A/T]CATACTGTGGTCCTC | 55632 |
rs568319119 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30594681 | CTGGGCCACAGAGCG[A/G]GACTCCATCTCAAAA | 55632 |
rs568355649 | in-del | -/TTG | | | intron-variant | G2E3 | GRCh38.p7 | 14:30567413 | AACCTATTGTTTAAT[-/TTG]TTAACTTTTAACTTC | 55632 |
rs568450148 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30578474 | ACCCACGCCAGTGAG[A/C]GAGAGTGCAAACAAG | 55632 |
rs568450222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30569873 | AACATCCCAGGCTTT[C/T]ACACACTGTTGTACC | 55632 |
rs568464040 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30617653 | GAATGAAAAACCCAT[A/T]CTAATGTCACCACTC | 55632 |
rs568471681 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30575538 | AGTCAGGCAAGAGAA[A/G]GAAATAAAGGGCATC | 55632 |
rs568473556 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30563595 | GGACATATGGAGCCA[A/G]TGGGTGGTAGGGTGG | 55632 |
rs568538280 | in-del | -/AA | 0.00318978 | 0.0398085 | intron-variant | G2E3 | GRCh38.p7 | 14:30615681 | AAAGAAAGTTATTTC[-/AA]AAAGCAAGTTTATAT | 55632 |
rs568614531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30564038 | CTTTTTATCTTAAAC[C/T]TATCCTTTTGTTTTA | 55632 |
rs568641988 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30585517 | ATTGATCTATATGTT[G/T]ATCCTTATGTCACTA | 55632 |
rs568690244 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30565966 | CACCTGGCCAACTTC[A/C]TTCTTATTTACATGG | 55632 |
rs568736484 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30599611 | CTTCAACATATGAAG[A/T]GGGGAGAGACACATT | 55632 |
rs568755582 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30559110 | GCGGGTCCCACCCCT[C/T]GAGGGCGGGGCCGAC | 55632 |
rs568781250 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30607296 | TATGTTCTGAGAAAT[A/G]TGTCAGTAGGCAATT | 55632 |
rs568798770 | snp | A/G | 1.77018e-05 | 0.00297499 | intron-variant | G2E3 | GRCh38.p7 | 14:30615578 | TTTAACGATCTCAGA[A/G]TATTTGTTTCAGCAT | 55632 |
rs568814361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30571937 | TAGAATCAGCATGCC[A/G]GTATCTTAAAAAAAA | 55632 |
rs568814980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30559809 | CAGTCTTTGAAATGC[C/T]TGAGTGGGATTTAAA | 55632 |
rs568887419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30580299 | GCAACCTCCACCTCC[C/T]GAGTTCAAGCAATTC | 55632 |
rs568938746 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30573609 | CAAACAGCTGATGGT[A/G]TAGGTTCCAGTCCGG | 55632 |
rs568950086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30572673 | TTACTTTTCAGATGA[C/T]ATCTAATCTTATATT | 55632 |
rs569030142 | snp | A/G | 1.64993e-05 | 0.00287218 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30601876 | TGTTTGGAATGTAGG[A/G]GTATTATCTACAATT | 55632 |
rs569063036 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30571630 | TTCCCCCCACCCTCC[A/G]CCCAAAGCATTCAGT | 55632 |
rs569102187 | in-del | -/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30609734 | TTTTTTGTTTGATTG[-/T]TTTTTTGTGGGGCTT | 55632 |
rs569109603 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30597401 | TCATTAACAGTAGAC[C/T]TTTTATTTTCCACTG | 55632 |
rs569168357 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30602759 | TGGAACTACAGATGC[A/T]TGCCACCATGCTTGG | 55632 |
rs569254294 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30563693 | TTGTAACTTTGTTAC[G/T]TTTGTGTGTGTGTGT | 55632 |
rs569255209 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30557259 | CGGGGTCATATTAGA[C/T]ATGTAAACATAAAAT | 55632 |
rs569286617 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30584426 | GTCATATGGTAACTC[C/T]TTGTTTAAATTTTGA | 55632 |
rs569289548 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30599796 | TTTTTAATGTGGCTA[A/C]TGGAAAATTTTAAAT | 55632 |
rs569309789 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | G2E3 | GRCh38.p7 | 14:30598206 | CCTTGCCAACATGGC[A/G]AAACCCTGTCTCTAC | 55632 |
rs569315331 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30564169 | TATTCTCTTGTATGA[A/C]TATACCACAGTTTGT | 55632 |
rs569362578 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30618342 | AGTTTTTATTCCAAA[C/T]ATGTTGATAAAAAGA | 55632 |
rs569376218 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30591282 | TCCCTGAATCAGTGA[A/C]CATTTTAATTGCCGT | 55632 |
rs569382756 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30591017 | GAGCATCATGTTGGC[A/G]CTCAGAAAGTTTCCT | 55632 |
rs569434856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30600639 | ATCAGTAGCTACAAC[C/T]CTTCTTTCCAGGACA | 55632 |
rs569536367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30593110 | AAACTATTTTTTAGG[C/T]GTAAGTTCCTGCCTC | 55632 |
rs569574625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30613679 | ATCAAGGGTTTTTAA[A/G]TCTATTTTAATCTAT | 55632 |
rs569636241 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30612597 | GGTGGCTCACTCACA[C/T]CTGTAATCCCAGCAC | 55632 |
rs569666745 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30614608 | TTCAACATGAGTTTC[A/G]AAGGAACTCATTTGA | 55632 |
rs569720296 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30612676 | CAGCCTGACCAACAT[A/G]GTGAAACCCCGTCTG | 55632 |
rs569739392 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30584694 | TCTTCTTTGGAGAAA[C/T]GTCTATTCAAATCTA | 55632 |
rs569740353 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30576872 | CTTTCAAGTGCCTGA[-/T]TCCAGCATGTTTTCT | 55632 |
rs569759273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30583940 | ATTTACAATGTTGTG[A/G]AACCATCACCACTAT | 55632 |
rs569891509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30568780 | AATAACATTGATTTA[C/T]ATTTATTTTACGTGT | 55632 |
rs569950657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30579063 | CTCAATCAATTTGTT[C/T]ACTTAAGGCAGTTCT | 55632 |
rs569985085 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30570467 | CTTGGACTCCTATTA[A/C]GCATATATTGGTATA | 55632 |
rs570016503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30562827 | CTAAAAGTCTTTGAT[A/G]TGCAGAAATAATGGT | 55632 |
rs570053859 | snp | C/G | 0.0444908 | 0.142359 | intron-variant | G2E3 | GRCh38.p7 | 14:30590333 | TTAGACTTTGTTTTC[C/G]ACAGATGCCAAAGTC | 55632 |
rs570169667 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | G2E3 | GRCh38.p7 | 14:30584852 | TTTTTTTTTTGAGAC[A/G]GAGTCTTGCTCTGTC | 55632 |
rs570207144 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30594904 | GAGGCCGAGGAGGGC[A/G]GATCACCTGAGGTCA | 55632 |
rs570237639 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30585180 | ATTTTAATGAAGTCC[A/C]ATTATCATTTTTTTC | 55632 |
rs570269025 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30562224 | GGGGGCACGAGCTGT[A/T]CCAGTATAATAAAAT | 55632 |
rs570292207 | snp | C/T | 1.66579e-05 | 0.00288595 | missense, intron-variant | G2E3 | GRCh38.p7 | 14:30605681 | AAGTAGCATATGTTA[C/T]TGAAAATGATAATTT | 55632 |
rs570294852 | in-del | -/TTATC | 0.00438332 | 0.0466095 | intron-variant | G2E3 | GRCh38.p7 | 14:30607836 | TATAAAAAATGATGG[-/TTATC]TTATAATAATAGAAG | 55632 |
rs570341709 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30567128 | AGAGATAATTGGCTT[A/G/T]TAGTTTTATTTTCTG | 55632 |
rs570357455 | snp | C/T | 0.031825 | 0.122064 | intron-variant | G2E3 | GRCh38.p7 | 14:30579539 | GTTTAATTTGGTTAA[C/T]CAGTCTTCATAAAAT | 55632 |
rs570417613 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30591204 | CATTGGGAGAGTTTC[A/G]GGTTGGCAGGTATTC | 55632 |
rs570426059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30599519 | GGCATGAGCCACTGC[A/G]CTCGGCCATAATTAC | 55632 |
rs570552969 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30614472 | AGGCTGAACTTACCC[G/T]TTTTATCAGGAGCTC | 55632 |
rs570681211 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30562867 | CTCTCTCTCTGCCTC[A/G]GCTGCCAGGCAGGGA | 55632 |
rs570713603 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30609703 | TGTTTAAGATAAAAA[G/T]AGTATTTTTCCCAGA | 55632 |
rs570731577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30571720 | CTTTGTTGAAAAGCA[A/G]TTGTCTGGGTCTGTT | 55632 |
rs570807849 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30576684 | ATTCTTTATTATGTA[G/T]GGGACATCCATAGAC | 55632 |
rs570849348 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30572080 | GCAGTGTTTTGTAGC[A/T]TTTCAGAGTGTAGTC | 55632 |
rs570859932 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | G2E3 | GRCh38.p7 | 14:30602196 | TATGATAGGAAATGC[A/C]ATATACATTTAGAAT | 55632 |
rs570861674 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | SCFD1, G2E3 | GRCh38.p7 | 14:30620406 | TGCATTTGAAAGTGG[A/G]AGTACCCAAATGAGC | 55632 |
rs570863621 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30610799 | ATTTTAGGGTAAGAG[G/T]TGGCAAAAAATGGCC | 55632 |
rs570889211 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30599181 | AACACCAGTCATTTG[G/T]TTTAGGGCCCACCTA | 55632 |
rs571064940 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30605927 | TATACTGTTCACTTT[C/G]TTAATAAACTACTGA | 55632 |
rs571131770 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | G2E3 | GRCh38.p7 | 14:30606437 | TTGAATTTCCTACTA[C/T]ATTTTCTGTAAACAT | 55632 |
rs571136343 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30567798 | GTGATTTCTTTTTTG[A/G]CTTTTTGTCTATTTA | 55632 |
rs571220884 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30614103 | ATAATAAGAATATAT[G/T]GAAAGTATATACAAA | 55632 |
rs571293461 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30604359 | TGGGACAGATTCATA[A/C]TTGGTATGGAAAATG | 55632 |
rs571324376 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30617681 | CTCAGAGATAAGTAC[C/T]GTATTTCTGTGTATC | 55632 |
rs571350742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30597186 | AGATTGAAAAAAATA[C/T]ATGGGTGATGTAAAG | 55632 |
rs571355219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30596245 | ATTCCCCAAGTGTAA[C/T]CAAGTCTACTTAGTA | 55632 |
rs571430885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30588392 | GTGTATCACTTGTTA[C/T]CACTTGTTTTTCTTT | 55632 |
rs571529070 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30590508 | CCCTTTCCTGCCCCT[C/G]TCCATGTCCCACCCC | 55632 |
rs571550514 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | G2E3 | GRCh38.p7 | 14:30603123 | CCGAGGTCAAGAGAT[C/T]GAGAACATCCTGGCC | 55632 |
rs571587275 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30591088 | ATATTCAACCTGTAC[G/T]TATTTTCTTAAAACA | 55632 |
rs571589371 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30583383 | ATCCTCATTTTTATG[A/T]TGAGGAAATGGAGTC | 55632 |
rs571603716 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30609747 | TGTTTTTTGTGGGGC[-/T]TTTTTTGTGTTTTTA | 55632 |
rs571672635 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30581467 | ATTCCAGCACTTTAC[A/G]AGGCTGAAGCAGGCA | 55632 |
rs571792387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30611002 | ATGGCCCTCTGTTTT[C/T]GAGATAGAGTTGTGA | 55632 |
rs571833867 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30565306 | ATTTTGTTCATTTTT[A/G]AGTTGGATTACTTGT | 55632 |
rs571856073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30574647 | GTTCTTATCATTTAG[C/T]TCCCACTTACAAGTG | 55632 |
rs571856749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30610487 | CAGGTGTGGTGGCGC[A/G]CGCCTATAGTCCCAG | 55632 |
rs571862832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30575599 | CTTTGCAGATTACAT[A/G]ATTCTGTATCTAGAA | 55632 |
rs571987912 | snp | A/G | | | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558875 | AGGTGACGAAACTTC[A/G]GCACATCTCTGTCCA | 55632 |
rs572011366 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30590080 | ATATAACAGCCACTA[G/T]GCTGTATGCAGGGAA | 55632 |
rs572013773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30589049 | TTAAGCTTAATTGTA[A/G]GTGTTCTTTCTTTCT | 55632 |
rs572088299 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30563100 | ACAATCTCTCGTCTC[C/T]GCACACGGGGAGAAA | 55632 |
rs572104440 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30581571 | AATTAGCCAGGAGGC[A/G]CATGCCTGTAATCCC | 55632 |
rs572200530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30582827 | AACCAGAGTGAGGGA[A/G]GGCAGAGTAGTTAGG | 55632 |
rs572214979 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30618911 | TATAAATGTGTACAT[A/G]TATTTCTTAAATATT | 55632 |
rs572226109 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | G2E3 | GRCh38.p7 | 14:30596407 | TCTTTAACTTACCTA[C/T]CTAGCCTCTACTTAG | 55632 |
rs572260013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30576123 | TCTTCAAACTATACT[A/G]CAAGGCTCCAGTAAC | 55632 |
rs572264809 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30569167 | AATTTATAAGAAATT[A/G]AAAGAAAAAGCCCCT | 55632 |
rs572322813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30576954 | GGATGGGGCCAGGCA[C/T]GATGGCTCACACCTG | 55632 |
rs572409404 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30585940 | TCCAGTTATTATGCA[C/G]AAGGTTTTCCAAATT | 55632 |
rs572448308 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30604624 | TGGGAGCACACTTTG[G/T]GACTTACTGATCTAG | 55632 |
rs572532159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30567441 | ACTTCTTAGAGTACA[A/G]TTGTTCATAATAGTC | 55632 |
rs572547938 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30589290 | AGCCATTTTATGTCT[C/G]TTTTTTATTAGACTG | 55632 |
rs572551924 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558715 | ACTGTGCCGGGATAG[G/T]ACTGAGAGGCCCAGG | 55632 |
rs572567001 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | G2E3 | GRCh38.p7 | 14:30619405 | ATTATAAGAAAATGA[C/T]CAGAACAAAATCATT | 55632 |
rs572585828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30560173 | TCTGTCTAACCCAGT[A/G]GTAAAGTCATGCCTT | 55632 |
rs572601775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30560796 | TCAGATTCTGAATCA[A/G]TAGGTCTGGAGGATG | 55632 |
rs572756445 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30565947 | TTACAGACGTGAGCC[A/G]CCACACCTGGCCAAC | 55632 |
rs572769420 | in-del | -/GG | 0.0182019 | 0.0936463 | intron-variant | G2E3 | GRCh38.p7 | 14:30569741 | GGACCAGCTGGTGAA[-/GG]GGGGGGGGATTATAT | 55632 |
rs572782289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30565384 | GACCCTTTTCAGGTT[A/G]TATGATTTCTGAATA | 55632 |
rs572800649 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30566037 | TTCTTCCCATTTAAT[C/G]GTCTTGGCACCCTTA | 55632 |
rs572857565 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30600360 | TTTAAATTTAATGCT[A/G]TTAAACCAAAAATTC | 55632 |
rs572955918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30601197 | TGGAGCCCTACACTA[C/T]AGCCCACACTTGTAG | 55632 |
rs572984978 | in-del | -/T | 0.0130921 | 0.0798413 | intron-variant | G2E3 | GRCh38.p7 | 14:30586664 | ACCAATTCCATAGGG[-/T]TTTTTTGAAATATTT | 55632 |
rs573018892 | snp | G/T | 1.65726e-05 | 0.00287855 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30602028 | GCCAAAAAACATGTA[G/T]TACCCAATTCTAATA | 55632 |
rs573024541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30594842 | AGTTAAAAGTGCAGG[A/G]TGAAGGCAGGGCACA | 55632 |
rs573058390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30593288 | AAAAGTTCAGATTTC[A/G]AAGGTCCAGCTCTCT | 55632 |
rs573088054 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30587951 | CAACAAATTGTGGAC[A/G]TATTTTCAAATCTAC | 55632 |
rs573120958 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30598391 | GACTGCGTCTCAAGA[A/G]CAAAAAAAGGTTTTT | 55632 |
rs573197122 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30600107 | ATAGGAAATTTCAAT[A/G/T]ATTTGTTATCACTGT | 55632 |
rs573418429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30571577 | TTTTTTCTTGTGATC[C/T]AATTTGAATTAAGTT | 55632 |
rs573470885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30586128 | AGAAAGTTCTGAGGC[A/G]GGTGAAAGAAAGGCA | 55632 |
rs573496674 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30609274 | TTCATTGTCTCTACT[G/T]CGTATTTCCTATTTA | 55632 |
rs573505336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30572229 | CTTATTCTTATAAAT[A/G]TGTTGGTAGGATTTT | 55632 |
rs573557760 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30559244 | AAAAGTGGCACTGAG[G/T]CTCTGGAACTTCTGC | 55632 |
rs573560522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30608686 | CATAATGCCATATAA[A/G]TGTCATTGCCAACAT | 55632 |
rs573592860 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30618083 | AAAGAGATAATATAT[C/T]TCTTAATACCAAAGG | 55632 |
rs573637392 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30574172 | GTTGGAGAGTAGGTT[C/G]CATATATCTGGTCCC | 55632 |
rs573782377 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30588053 | CTACAGTCTTGTGCC[G/T]CCGTACCTCAAAGGT | 55632 |
rs573817562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30588775 | TTATTCACATTCTAC[A/G]CTTTCTCTGATTCAG | 55632 |
rs573844339 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30581615 | GCCGAGGCAGGAGAA[C/T]CGCTTGAACCCGGGA | 55632 |
rs574043864 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30586184 | GCCATCATACAGGTC[A/G]AAACAATCACATTTT | 55632 |
rs574083786 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30578646 | AATGACTAAAACATC[A/C]TTTATAAATTAAACT | 55632 |
rs574105229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30580174 | CAACAGCCACAAATA[C/T]GGTATAGACTAATAA | 55632 |
rs574209178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30571394 | TTGCCAGTGTTTATT[C/T]CCAATCTGTGTTTTG | 55632 |
rs574278444 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30572271 | ATCATATGTGAAAAC[A/T]GTTTTACTTCATCCT | 55632 |
rs574339756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30565535 | ACAAGGTCATGAAAA[C/T]TTACCCCTAGATTTT | 55632 |
rs574399701 | snp | A/G | 0 | 0 | intron-variant | G2E3 | GRCh38.p7 | 14:30566116 | TTCTTTTCTATTGAT[A/G]TGTATGTCTGTCCTT | 55632 |
rs574463609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30563846 | TGCCTCAACCTCCTG[A/G]GTAGCTGGATTACAG | 55632 |
rs574550820 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30564434 | AACTCTTGGACTCCA[G/T]CTGTCCTCCCACCTC | 55632 |
rs574616942 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30563811 | TGCAACCTCCGCCTT[C/G]CCGGTTCCAGTGATT | 55632 |
rs574617998 | in-del | -/TA | 0.00159617 | 0.0282053 | intron-variant | G2E3 | GRCh38.p7 | 14:30581938 | CTTTTAAATTCACTC[-/TA]AAATTAAAATATTAT | 55632 |
rs574659815 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30613767 | GATAATTCTAATTCA[C/G]ATTCTCTATTGCATG | 55632 |
rs574718060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30562524 | GAAGACGCCCGTTGC[C/T]AAGAGGACCATGGTC | 55632 |
rs574818755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30577985 | TGTTATTGAACTATA[C/T]ACTTAGATATTATTT | 55632 |
rs574901971 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30605270 | TCAACTTTCTTGTAC[A/G]TGATTCTAATTTGGT | 55632 |
rs574903723 | snp | A/G | | | synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30601848 | ATTACGGTCATGGGA[A/G]CAAAATTGGGAGTGT | 55632 |
rs574945510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30615081 | GTTTTGAAACTATAA[A/G]GCCAAATAATGTAGG | 55632 |
rs574996896 | snp | C/T | | | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558823 | AAGATAAAACCCTCC[C/T]GCCTCCGTTCGTGCT | 55632 |
rs575045540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30591826 | GAGTCGGGACCTGAG[C/T]ATAACTTTTTGGAGA | 55632 |
rs575077204 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558582 | TCTAACACCATCAAA[C/T]AGTTTATTTGAGACC | 55632 |
rs575094417 | in-del | -/TCTATG | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30572244 | ATGTTGGTAGGATTT[-/TCTATG]TAGATGATCATATGT | 55632 |
rs575106181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30584934 | CCTCCCAGGTTCAAG[C/T]AATTCTTCTTCCTCA | 55632 |
rs575124116 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30568369 | ATTCATTCTGTCAAC[C/T]TTTGCCTTTTAATTG | 55632 |
rs575190293 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30586256 | TCTGCACCAGGAACA[C/T]GGGCCACCCCAAGAC | 55632 |
rs575405853 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | G2E3 | GRCh38.p7 | 14:30601042 | ACAGAAATTAACATA[C/T]GCACACCCACACAGA | 55632 |
rs575438122 | snp | A/G | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30577397 | TGGTTTTAAACAATA[A/G]ACATTTAATTACTGA | 55632 |
rs575537922 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30572840 | AGCTTCTAGTTTGAG[A/G]GATGATAAAATTGAG | 55632 |
rs575553864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30570853 | TTTGAAGAGTTTTTT[C/T]AGAAAATATATTGTG | 55632 |
rs575605717 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | G2E3 | GRCh38.p7 | 14:30606645 | AGTTTGTACACATCT[A/C]GTTCTTTACATCCTT | 55632 |
rs575684637 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30591010 | TTCCTTTGAGCATCA[C/T]GTTGGCACTCAGAAA | 55632 |
rs575718827 | snp | G/T | 1.64768e-05 | 0.00287021 | synonymous-codon, intron-variant, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30598525 | CGCTTATCAAGAGCT[G/T]CTGCAGCACTATGAG | 55632 |
rs575764290 | snp | A/G | 0.000168498 | 0.00917717 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30608029 | CCCAGCCAATTTTAG[A/G]TGATGTTTCAGACTT | 55632 |
rs575780903 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30591516 | AAGTGTCAAAAGGGT[A/T]CCTTCTAGAGGCACT | 55632 |
rs575842506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30591879 | GTCTCAACACTTTTT[C/T]ATTTGGTCAGAATAG | 55632 |
rs575907563 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | G2E3 | GRCh38.p7 | 14:30567628 | TTCTCAATTTAAAAA[A/T]TTTTTTATTACATTA | 55632 |
rs575924551 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616928 | TTTATTCAATTTTCA[A/G]ATTATTCCTCATTTT | 55632 |
rs575969449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30585412 | TATTTGTTGATGAGA[C/T]TATTCTTTCACCATT | 55632 |
rs576083543 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30567493 | TATTAGGTCTGTAGC[A/T]GTGTCCCACTTTCAT | 55632 |
rs576085902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30577002 | GAGGCAGAGGCAGGC[A/G]GATCATGAGGTCAAG | 55632 |
rs576169829 | snp | G/T | | | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30557339 | AATTGTAGAAAGAAC[G/T]GTTGAATGAATGAAT | 55632 |
rs576296852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30569328 | CTTCTCCTGCTTTGC[A/G]TATAAGAACCCTAAT | 55632 |
rs576302660 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30596371 | GCCTTAGTCCCTATC[A/C]ATTTATTCTTCATAC | 55632 |
rs576330577 | in-del | -/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30585006 | CAGCTAATTTTTGTA[-/T]TTTTTTTTTAGTAGA | 55632 |
rs576358860 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30569969 | TTACGTTATAATATC[A/C]CCACCTCTGTAAGGC | 55632 |
rs576364059 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30590192 | ATACTGGCATTAATG[A/T]TTTTCATGGGGGAGC | 55632 |
rs576367955 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30597264 | AGATTTTAGCAGTGG[G/T]ATAACTTAGTTTATA | 55632 |
rs576372930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30613999 | TAAATTGCATTTTCA[C/T]TTTTTATTTTTAGTG | 55632 |
rs576424133 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | G2E3 | GRCh38.p7 | 14:30562915 | GGACACGTGACCCAC[A/G]TGAACTTACCTATCA | 55632 |
rs576487012 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30564286 | CTCTTGGCTGCATCA[G/T]ATGATAGGTGTACAT | 55632 |
rs576506179 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | G2E3 | GRCh38.p7 | 14:30565180 | AGCTATTATAGTGGA[A/C]ATGAAGTGGTGTCTC | 55632 |
rs576539289 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30561514 | CATCTTCATAATATT[A/C]CACCAGTCTCTTCCA | 55632 |
rs576569570 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30589857 | CCCAACCATATACTT[C/T]TTTATTCTTATACCT | 55632 |
rs576574307 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30604713 | AATTATGACTTTATG[A/T]TTTAAAATATATTGT | 55632 |
rs576691669 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30588750 | AGCCTGGCTTGCAAG[C/T]CAGGATTTCTTATTC | 55632 |
rs576728293 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30560395 | GGACTTCATAATAAT[C/G]AGAATAAAAACATTC | 55632 |
rs576771747 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30607812 | TTAGATTTTTGGACT[A/G]ATTTTTAATATAAAA | 55632 |
rs576825598 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | G2E3 | GRCh38.p7 | 14:30577731 | CATTTCTGCCACAGT[C/G]TTTTTTGTTGAAGCA | 55632 |
rs576872198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30561639 | TTAAGATTTTACTCA[A/G]ATGGGTTTAAAGACT | 55632 |
rs576888035 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30570076 | AACATAGTTTTGCTG[A/C]AGATAGGATTCTTTG | 55632 |
rs576907277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30614968 | TGAAGATTTATCACT[C/T]TTGGTAATATCTGGG | 55632 |
rs576955152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30570569 | ATAATTTCAACTAAC[C/T]TGTCTTCAAGTTCGC | 55632 |
rs576968054 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30614066 | TATATAAAATGTTTT[A/T]TATAGTTCCAAAGTC | 55632 |
rs577000190 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30566784 | TGTTCCAGATCTTAG[C/G]TGGAAAGTGTGCAGT | 55632 |
rs577012673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30563797 | GGATCTTGACTCACT[A/G]CAACCTCCGCCTTCC | 55632 |
rs577097790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30563106 | TCTCGTCTCCGCACA[C/T]GGGGAGAAAAACCCA | 55632 |
rs577106669 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | G2E3 | GRCh38.p7 | 14:30599322 | AACCTCTGCCTCCCG[A/G]GTTCAAGCAGTTCTC | 55632 |
rs577150075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30567993 | GTGCATTTGAGAAGA[A/G]TGTTTCATTCTGTTG | 55632 |
rs577189507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30611959 | TTTCAATGTCAGTTA[C/T]TTCCTTTTTTATAAA | 55632 |
rs577212652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30568979 | AAGTTTCCCTTTCAC[C/T]CTAGACCCCAGGTCT | 55632 |
rs577250596 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30604855 | CCATTAGCCAGGAAG[A/C/G]TGAGAGTTTGAGCTT | 55632 |
rs577297750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30609354 | TTCATAGTTTATATC[C/T]AGGGAGCTAAATATC | 55632 |
rs577311486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30596411 | TAACTTACCTACCTA[A/G]CCTCTACTTAGTTCA | 55632 |
rs577341089 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30582497 | CATACAGCAGATGTA[A/C]CTCCATCCAGGGTTC | 55632 |
rs577438224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30598243 | ATACAAAAACCAGCC[A/G]GGCATGGTGGCAGGC | 55632 |
rs577489789 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30565939 | GTGCTGGATTACAGA[C/T]GTGAGCCACCACACC | 55632 |
rs577498742 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30591362 | TTGATTCATTTAATA[A/T]TTTTTCTATTTATGT | 55632 |
rs577533483 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30599789 | TTTATATTTTTTAAT[A/G]TGGCTACTGGAAAAT | 55632 |
rs577574215 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30594956 | CAACATGGTGAAACC[C/G]TTTCTCTACTAAAAA | 55632 |
rs577574645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30603593 | ATACCTGTAATCCCA[A/G]CAGTTTGGGAGGCTA | 55632 |
rs577596527 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30604650 | TCTAGACTAAAAGGT[A/G]CTATTTTAGGAATTG | 55632 |
rs577636217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30595614 | GTCTATGATGTAAGA[A/G]ATATCACTAAGCAAT | 55632 |
rs577682647 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | G2E3 | GRCh38.p7 | 14:30560691 | TCATTGGATTTTTGC[C/T]CTTTCTTAAATCAGT | 55632 |
rs577779943 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30579115 | ATAAACATCAAAAGC[G/T]CCATCGTATACCTGT | 55632 |
rs577824656 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30575254 | GCTTATGTCCTTTGG[A/C]CACTTTTTAATGGGG | 55632 |
rs577889237 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30567618 | ATTTTATTGATTCTC[A/C]ATTTAAAAATTTTTT | 55632 |
rs577971118 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30582711 | AATGGCAATTTGCTG[G/T]AGTTAATGTGAACAG | 55632 |
rs577997889 | snp | A/C | | | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616287 | TTTCAGATGGTAAAT[A/C]TACAACAACAATGGA | 55632 |
rs578028585 | in-del | -/A | | | intron-variant | G2E3 | GRCh38.p7 | 14:30608981 | GGGAGACACTGTCTC[-/A]AAAAAAAAAGCACAG | 55632 |
rs578064254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30573022 | CTTTTTTTTTGGATG[A/G]AGGTCTCACTATGTT | 55632 |
rs578073958 | snp | G/T | 0.00159617 | 0.0282053 | downstream-variant-500B | G2E3 | GRCh38.p7 | 14:30620069 | TAAGCCAAAAATCTG[G/T]ACTCAGATAAATGGC | 55632 |
rs578097611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30573904 | CCTGGTAAAGGTAAC[A/G]CATAAAATTAACCAT | 55632 |
rs578228886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | G2E3 | GRCh38.p7 | 14:30602982 | AATGTCAGCTCTTCC[C/T]TTTAGAAAGTTTAAG | 55632 |
rs745320394 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30586505 | GCCATTTTAACTACA[C/T]AGTGAAATTCATCAT | 55632 |
rs745349733 | snp | A/G | 1.68545e-05 | 0.00290292 | intron-variant | G2E3 | GRCh38.p7 | 14:30601932 | TAAAGTTTTTATTCA[A/G]ATGTATATGATTTAA | 55632 |
rs745352962 | snp | A/G/T | 6.82587e-05 | 0.00584169 | utr-variant-5-prime, missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30586753 | CATGATGACTGTCCT[A/G/T]ATAAATACGGAGAAA | 55632 |
rs745366913 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30575690 | GGATGCAAAATCAAC[A/G]TACAAAATTCACTAG | 55632 |
rs745371773 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30598813 | TCTGTTGTCTTATCA[C/T]GAGACTATTTTCTAG | 55632 |
rs745372967 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30585055 | TGGGCAGGCTGGTCT[C/T]GAACTCCTGACCTTG | 55632 |
rs745420254 | in-del | -/GAAG | | | intron-variant | G2E3 | GRCh38.p7 | 14:30578042 | AAAATTCATATTCTT[-/GAAG]GAAAACATCTAAAAG | 55632 |
rs745437632 | snp | A/C/T | 0.000132195 | 0.00812906 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30615408 | AGGCTTATCCAGAAG[A/C/T]ATTTTGTAGCATCCT | 55632 |
rs745491947 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30613264 | CTTGTTATTGACTCC[A/G]GTATTATTTTAAAGC | 55632 |
rs745548541 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30568622 | CTTAAACTTATAACA[A/G]CCTAGTTTGAATTAA | 55632 |
rs745574187 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30611678 | CTTTTCTTTTTAAGA[C/G]ATAAGGTCTCAGTCT | 55632 |
rs745625324 | snp | A/G | 1.65176e-05 | 0.00287376 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30612276 | AACTACCTTGAGTTA[A/G]TTGGATGTCTCAGAC | 55632 |
rs745632649 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30589846 | TCCTGAGTCAACCCA[A/G]CCATATACTTTTTTA | 55632 |
rs745720849 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30578898 | TTTTTCTTGTACCAT[C/T]TGTTTAAAAGATTTT | 55632 |
rs745757850 | snp | G/T | 1.80286e-05 | 0.00300233 | intron-variant | G2E3 | GRCh38.p7 | 14:30592471 | TTTAACTGTTAAATA[G/T]GAAAGTTCAGTGTTA | 55632 |
rs745834577 | snp | A/T | 1.80179e-05 | 0.00300143 | missense, intron-variant | G2E3 | GRCh38.p7 | 14:30605583 | AAAAAAAACTAAAAG[A/T]TTGTATATCAACAAA | 55632 |
rs745864842 | in-del | -/T | | | utr-variant-3-prime, downstream-variant-500B | G2E3 | GRCh38.p7 | 14:30619803 | ACATTTATAACAATG[-/T]TTTATAAATAAATAA | 55632 |
rs745953921 | in-del | -/A | | | intron-variant | G2E3 | GRCh38.p7 | 14:30590058 | AGTTATCATTTGTGC[-/A]TCTTCTATATAACAG | 55632 |
rs746004356 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30570007 | CATGTGTGTGAAATA[C/T]TTGTTTACTTGCCTG | 55632 |
rs746023298 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30582032 | ATAAGGAAATTTATG[C/T]TCCTAAACCTCTTCT | 55632 |
rs746064837 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30594314 | GATGAACTTAAGTTT[A/C]ATACTGTTTTTTAAA | 55632 |
rs746122872 | snp | C/T | 1.65056e-05 | 0.00287272 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30597436 | TTCAAGCAATAAATG[C/T]GGGAGTGTTTTTCTT | 55632 |
rs746149929 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30564094 | AGTATCTGGTATACA[A/G]TTTGTATGCAATAAA | 55632 |
rs746172836 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30609830 | AGTCATTTTCATACT[A/C]CTCCATTTTCCAGTT | 55632 |
rs746227414 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30559384 | GGGGCCTCGCAGTGC[C/T]TTTGGGGACGTCTGG | 55632 |
rs746244548 | in-del | -/AT | 1.76905e-05 | 0.00297404 | intron-variant | G2E3 | GRCh38.p7 | 14:30615578 | TTTAACGATCTCAGA[-/AT]ATTTGTTTCAGCATA | 55632 |
rs746301009 | snp | C/G | 2.03872e-05 | 0.00319267 | missense, intron-variant | G2E3 | GRCh38.p7 | 14:30605809 | TTGTCTCTAAATTCT[C/G]AAGGTAATTATTTTA | 55632 |
rs746350429 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30575461 | ATTCCTCTTGAGAAC[C/T]GACACAAGACGAGGA | 55632 |
rs746400140 | snp | A/C | 3.35509e-05 | 0.00409564 | intron-variant | G2E3 | GRCh38.p7 | 14:30589334 | TATATTTTTTTAATG[A/C]CCAACTAGTTTCTTA | 55632 |
rs746409036 | snp | G/T | | | upstream-variant-2KB, intron-variant | SCFD1, G2E3 | GRCh38.p7 | 14:30620460 | ATATTTCATAGAGAC[G/T]GTAGAATGCAGTAGA | 55632 |
rs746520611 | snp | C/T | 1.71366e-05 | 0.00292712 | intron-variant | G2E3 | GRCh38.p7 | 14:30589528 | TGTCATAAATATTGT[C/T]AATACTTGGGAAGTC | 55632 |
rs746581379 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30575695 | CAAAATCAACATACA[A/G]AATTCACTAGCATTC | 55632 |
rs746606018 | snp | A/G | 1.65252e-05 | 0.00287443 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30602055 | AATAATGTGGGGATT[A/G]CAGATTGTTTGTTGG | 55632 |
rs746647515 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30600001 | TTTTGTGCATTTGAG[G/T]TACAGTGTACTGTGT | 55632 |
rs746693778 | snp | A/T | 1.69266e-05 | 0.00290913 | intron-variant | G2E3 | GRCh38.p7 | 14:30601946 | AAATGTATATGATTT[A/T]AAAGTTTTTACCTAT | 55632 |
rs746748543 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30616155 | TAGTTTGCCCAAAAC[A/G]AATGTGGGAGTCTGT | 55632 |
rs746775640 | snp | A/C/G | 3.29974e-05 | 0.00406175 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30615438 | TGTGTCATAAACCTG[A/C/G]GAGTCTTTCTGCAAA | 55632 |
rs746836207 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30568678 | AAAAATTACACTTCT[G/T]TATATCTCATCCTTC | 55632 |
rs746859328 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30580678 | ATAATTTGTTAATAT[A/G]TAAAATGGGCTTAGG | 55632 |
rs746946067 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30611778 | TTCTACCTCATCTTC[C/T]AGAGTAGCTAGGACT | 55632 |
rs747040199 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30559524 | GGAGGCCCTGCCGGT[A/C]CCCCGCGAGTAAACC | 55632 |
rs747047390 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30604021 | TTACAAATATTGTTA[C/T]AACACTTTTAGTATC | 55632 |
rs747068253 | snp | C/T | 6.77576e-05 | 0.00582015 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616563 | ACAAAGAGAAGCTTC[C/T]TTAAAAGCTGCTATT | 55632 |
rs747076363 | in-del | -/AAT | | | upstream-variant-2KB, intron-variant | SCFD1, G2E3 | GRCh38.p7 | 14:30620380 | GAACTGAAGTGGCTC[-/AAT]GATGGATTTGCATTT | 55632 |
rs747158328 | snp | C/T | 3.32734e-05 | 0.00407868 | synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616417 | AAACAAGTGTAATAA[C/T]TGTTTAGCAATTCCC | 55632 |
rs747163533 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30571006 | TTTTTTTGTCTTGTG[A/C]TGTCAGTATTGTATC | 55632 |
rs747168934 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30572065 | CTTTCATTTCTCTCA[G/T]CAGTGTTTTGTAGCT | 55632 |
rs747271222 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30564983 | AATATTTCAATTGTT[C/T]TGGTTACATAGCTAG | 55632 |
rs747328072 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30595711 | GTTCCAATAACTTTT[A/G]TACTCTGGTATCGGT | 55632 |
rs747329639 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30582245 | ACTTCATTATTGTAA[C/T]AGAAACCAGTATCAT | 55632 |
rs747343568 | snp | C/T | 1.68156e-05 | 0.00289957 | intron-variant | G2E3 | GRCh38.p7 | 14:30598449 | ATGTAACATTATTTA[C/T]AGGTCAAAGCATATT | 55632 |
rs747380996 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30594716 | AAAGATGTAAATTCT[C/T]TTATTTCAATAAAGT | 55632 |
rs747388268 | snp | A/G/T | 0.000108082 | 0.00735053 | intron-variant | G2E3 | GRCh38.p7 | 14:30608104 | ATTAAAATGCACACT[A/G/T]CATTCTAGGTATCTT | 55632 |
rs747433491 | snp | G/T | 1.6507e-05 | 0.00287284 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30597457 | TGTTTTTCTTTAGGT[G/T]TACAATATGCAATAA | 55632 |
rs747448536 | in-del | -/AG | | | intron-variant | G2E3 | GRCh38.p7 | 14:30607276 | TTGTCACTTAGTAAC[-/AG]GGATATGTTCTGAGA | 55632 |
rs747508767 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30608220 | GTGGAGTTCTGAACC[A/T]GTTAAAAGATAGTTT | 55632 |
rs747512646 | in-del | -/GCTCAC | | | intron-variant | G2E3 | GRCh38.p7 | 14:30594422 | AGGCCGGGTGTGGTG[-/GCTCAC]GCCTGTAATCCCAGC | 55632 |
rs747538481 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30609103 | TTCTAAATCACACAG[C/T]AAGCACTATTGAAGT | 55632 |
rs747552425 | snp | C/T | 3.31175e-05 | 0.00406911 | synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30607946 | CATTTCTTTAGTTCA[C/T]GGTGGTCCTTCACCT | 55632 |
rs747552615 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30611033 | TTTACAAAACCGTCT[A/G]AGGACTTGAGTTCCT | 55632 |
rs747572044 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30595038 | AGCTACTTAGGAGGC[A/G]GAGGCAGGAGAATCG | 55632 |
rs747638927 | snp | G/T | 1.80784e-05 | 0.00300648 | intron-variant | G2E3 | GRCh38.p7 | 14:30608113 | CACACTACATTCTAG[G/T]TATCTTTTAATGTAA | 55632 |
rs747658299 | in-del | -/C | 1.64795e-05 | 0.00287045 | intron-variant | G2E3 | GRCh38.p7 | 14:30589502 | AAGTAAATTATTTTA[-/C]TATTAAGTAATGTCA | 55632 |
rs747679102 | snp | C/G | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30577427 | ATAGTTTCTGTTGAT[C/G]AGGGATTTGGGAGCT | 55632 |
rs747737535 | snp | C/G | 1.65078e-05 | 0.00287291 | intron-variant | G2E3 | GRCh38.p7 | 14:30592319 | TTTTCACATACTCTT[C/G]TAGAAATGCTGTGTT | 55632 |
rs747775633 | snp | A/G | 1.65086e-05 | 0.00287298 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30589428 | AAAGAAGAAGAAGGA[A/G]TTTATGGTTTTCTAA | 55632 |
rs747823537 | snp | A/G | 0.000186029 | 0.00964261 | intron-variant | G2E3 | GRCh38.p7 | 14:30590705 | AGGTTCTAGGGCACA[A/G]GGAAGAACCGTGGGA | 55632 |
rs747889987 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30587790 | AAGTGATGAGAGAGA[A/C]AGAGAGAGAGAAATC | 55632 |
rs747910080 | snp | A/G | | | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558548 | CCTTATCTGAGGGGG[A/G]AAATAAAATTTATTG | 55632 |
rs747921640 | snp | C/G | 3.30497e-05 | 0.00406494 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30602058 | AATGTGGGGATTACA[C/G]ATTGTTTGTTGGAAG | 55632 |
rs748017950 | snp | A/G | 0.000151828 | 0.00871155 | intron-variant | G2E3 | GRCh38.p7 | 14:30601968 | TTTACCTATATCTCT[A/G]TTATGCTAACATGGA | 55632 |
rs748025644 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30615731 | AGAAAAGATTACAGA[A/G]TAAATTTATATTTTG | 55632 |
rs748040270 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30598874 | CCACATGTGGCTGTT[A/G]AGCACTTGAGATTTC | 55632 |
rs748044271 | snp | A/G | 1.64961e-05 | 0.00287189 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30615452 | GAGAGTCTTTCTGCA[A/G]AAATCCTTAGTGAGC | 55632 |
rs748067364 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30569957 | TATTTTTCACAATTA[C/T]GTTATAATATCACCA | 55632 |
rs748078171 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30595034 | TCCCAGCTACTTAGG[A/G]GGCGGAGGCAGGAGA | 55632 |
rs748108148 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30568453 | TTAGTATTTGTTTTC[C/T]AAATACTATCTTTCT | 55632 |
rs748150450 | snp | A/G | 1.66685e-05 | 0.00288686 | synonymous-codon, intron-variant | G2E3 | GRCh38.p7 | 14:30605724 | TCCTGGATCAAAGCA[A/G]GAATTTCTGAGTCTC | 55632 |
rs748199143 | snp | A/G | 1.81955e-05 | 0.0030162 | intron-variant | G2E3 | GRCh38.p7 | 14:30592483 | ATATGAAAGTTCAGT[A/G]TTAAAGAATAGTGGA | 55632 |
rs748247033 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30590944 | ATATTTGCTTACCAG[C/T]TGAGCACCTCTAATC | 55632 |
rs748274744 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30560803 | CTGAATCAGTAGGTC[C/T]GGAGGATGGCATTGA | 55632 |
rs748310708 | in-del | -/AT | | | intron-variant | G2E3 | GRCh38.p7 | 14:30563372 | GTTGGTCTAAGGGAC[-/AT]AAAGCCCCATACCAC | 55632 |
rs748399648 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30573646 | AGGCCTGAGAACCAG[A/G]AACACCAAGGACAGA | 55632 |
rs748404047 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30584956 | TCTTCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 55632 |
rs748449973 | snp | A/T | 5.476e-05 | 0.0052323 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30586725 | ACTGTTAGCTTGTGT[A/T]TTCTGTCGAAAACAT | 55632 |
rs748455161 | snp | G/T | 3.32513e-05 | 0.00407732 | intron-variant | G2E3 | GRCh38.p7 | 14:30581044 | TGAGACTTTTACAAT[G/T]AAGATGACTGTATTA | 55632 |
rs748548979 | snp | A/C | 1.64751e-05 | 0.00287007 | synonymous-codon, intron-variant, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30598553 | GAGCGTTGTGATGTT[A/C]GAAGATGTCGTTGCA | 55632 |
rs748613497 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30583695 | ATGTGAAGTAATGCA[C/T]ATGATAATTAGCTCC | 55632 |
rs748666825 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30595750 | AAATAACATATGGAG[A/T]CTTATCCAATCTAGA | 55632 |
rs748689535 | snp | A/T | 1.65326e-05 | 0.00287507 | synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30612230 | TGCAACAACTGTAGC[A/T]GACTTAAAGTCAATA | 55632 |
rs748706647 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30583722 | CTCCATTTAGCTGTT[C/T]CACAATATGTACATA | 55632 |
rs748723769 | snp | A/G | 1.66012e-05 | 0.00288103 | intron-variant | G2E3 | GRCh38.p7 | 14:30598479 | TTTATATCTTCTTTT[A/G]TAGAGATGCTTCCTG | 55632 |
rs748731550 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30606453 | ATTTTCTGTAAACAT[A/C]CTAACCATTGCCTAA | 55632 |
rs748765355 | snp | C/T | 1.64743e-05 | 0.00287 | missense, intron-variant, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30598590 | GGCGAGACTATAATG[C/T]ACCTGATAGGTATTT | 55632 |
rs748766307 | snp | C/G | 0.000165382 | 0.00909196 | intron-variant | G2E3 | GRCh38.p7 | 14:30597376 | TATATCACCTGATAA[C/G]AGATTTAAATCATTA | 55632 |
rs748807585 | snp | C/T | 1.74254e-05 | 0.00295168 | intron-variant | G2E3 | GRCh38.p7 | 14:30612394 | GGTAAGTTGTTTCTA[C/T]TAATATATGGCTCTT | 55632 |
rs748817222 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30611587 | TCTTTTAATTCTCAG[C/G]TGTTACTCTTTTTCA | 55632 |
rs748903245 | in-del | -/ATAATT | 1.70507e-05 | 0.00291977 | cds-indel, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30593518 | AAATAATTACATCTA[-/ATAATT]ATAGAGAGTCCTTAC | 55632 |
rs748904729 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30578265 | ATAATCAACTTTTAG[A/G]TAATTTGATACTGCT | 55632 |
rs748928067 | snp | A/G | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30576091 | AAAGAACAAAGCTGG[A/G]GGCATCACATTACCC | 55632 |
rs748940297 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30610641 | TACATACATGCATAC[A/G]TACAACAGAATAAAA | 55632 |
rs748991275 | in-del | -/TCTTC | 3.77117e-05 | 0.00434217 | intron-variant | G2E3 | GRCh38.p7 | 14:30615337 | TTGGCTCATTATTTT[-/TCTTC]TCTTAAGTTTTAAGC | 55632 |
rs749039913 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30589962 | TATCTCCTGACCCTT[A/C]TCTAACATTGTGTGA | 55632 |
rs749059062 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30590784 | TATTAGTATCATAAT[G/T]CCTAAACTTCCTGGT | 55632 |
rs749078341 | snp | A/G | 3.30153e-05 | 0.00406283 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30592356 | AAAAATGGTGCTTCA[A/G]TTGGATGTGTTGCAC | 55632 |
rs749141476 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30559268 | CTTCTGCCCAGCTCT[C/T]CTTGGTGAGTAAATG | 55632 |
rs749164265 | snp | A/G | 3.55303e-05 | 0.00421472 | intron-variant | G2E3 | GRCh38.p7 | 14:30602182 | TATTTGGAGAAAATT[A/G]TGATAGGAAATGCCA | 55632 |
rs749224389 | snp | C/G | 1.66335e-05 | 0.00288383 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616395 | TGCATGTGGATTTTC[C/G]TGTTGGAAACAAGTG | 55632 |
rs749271893 | snp | C/T | | | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558640 | ACTTTTGGCTGAATA[C/T]GGGTGAACTTGGCTT | 55632 |
rs749323899 | snp | C/T | 1.65217e-05 | 0.00287412 | intron-variant | G2E3 | GRCh38.p7 | 14:30597411 | TAGACTTTTTATTTT[C/T]CACTGTAGGTTCAAG | 55632 |
rs749331109 | snp | A/G | 3.38163e-05 | 0.00411182 | intron-variant | G2E3 | GRCh38.p7 | 14:30581167 | GAGTGTTTTAAATAT[A/G]TTACTTAAACATTAG | 55632 |
rs749401153 | in-del | -/AAAAT | | | intron-variant | G2E3 | GRCh38.p7 | 14:30575378 | GAGGGAACATACCTC[-/AAAAT]AATAAGAGCCATCTA | 55632 |
rs749404673 | in-del | -/CTTC | | | intron-variant | G2E3 | GRCh38.p7 | 14:30589707 | ACAATACTGACTTCA[-/CTTC]CTTATCTTATTCCAA | 55632 |
rs749414706 | snp | A/G | 3.51525e-05 | 0.00419225 | intron-variant | G2E3 | GRCh38.p7 | 14:30607857 | TATAATAATAGAAGT[A/G]TATTTGATATATTTT | 55632 |
rs749471272 | snp | C/T | 1.6628e-05 | 0.00288335 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30593614 | CTTGTTGTAAGAACG[C/T]TTGGTTTCATAGAGA | 55632 |
rs749515766 | in-del | -/TAGGGATCTACTTCT | | | intron-variant | G2E3 | GRCh38.p7 | 14:30583151 | GCACCCTTCATCTTG[-/TAGGGATCTACTTCT]TAGGGATCCTGTCTT | 55632 |
rs749578351 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30605392 | TGGGAATTGGGGAAG[A/T]ATATCCTATTAATCT | 55632 |
rs749597729 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30561059 | CTTTGTAGGATTATT[G/T]TGAGGATTGAATGAG | 55632 |
rs749639690 | in-del | -/AGGT | | | intron-variant | G2E3 | GRCh38.p7 | 14:30603923 | ACTGGATTTGCAGAC[-/AGGT]AGAATATTAAGTACT | 55632 |
rs749671065 | snp | G/T | | | downstream-variant-500B | G2E3 | GRCh38.p7 | 14:30620237 | TATTTTTCTATAAAT[G/T]TATTGCCCACATTCT | 55632 |
rs749729934 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30574145 | TTGCATGTAACTTCC[C/T]TTTTCTGAACCGTTG | 55632 |
rs749778936 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30584991 | CACACACCACCATGC[C/T]CAGCTAATTTTTGTA | 55632 |
rs749789056 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30588347 | CATTTTATGTGTCTG[C/T]AGGTTATGTTTTCAT | 55632 |
rs749795952 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30619142 | CTCACCAGAAACTTA[C/G]AATTTTATACTTTGT | 55632 |
rs749824060 | snp | A/G | 1.65682e-05 | 0.00287817 | intron-variant, synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30581094 | AATGAATGAAAGTAA[A/G]CCTGGTGACTCACAG | 55632 |
rs749852878 | snp | C/T | | | synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616378 | TCCTTCAATTGAGTG[C/T]CTGCATGTGGATTTT | 55632 |
rs749865718 | snp | A/G | 1.70281e-05 | 0.00291783 | intron-variant | G2E3 | GRCh38.p7 | 14:30615542 | CAGGCTGTTGAAGGT[A/G]TGTGGATATTTTATT | 55632 |
rs749977503 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30608445 | TGGAGGCCGATGGGT[C/T]TGAAGAGAGGAAGGA | 55632 |
rs749981497 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30569714 | ATAAGACCTGCCCAC[A/G]AAGTCAGGGTTAGGA | 55632 |
rs750077440 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30580577 | TTTTTCTTTTTTCCT[A/C]AATGATGAACAATTC | 55632 |
rs750119984 | in-del | -/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30563693 | TTGTAACTTTGTTAC[-/T]TTTGTGTGTGTGTGT | 55632 |
rs750129037 | snp | A/T | 3.30759e-05 | 0.00406655 | intron-variant | G2E3 | GRCh38.p7 | 14:30597373 | TAATATATCACCTGA[A/T]AACAGATTTAAATCA | 55632 |
rs750131939 | snp | A/G | | | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30593526 | ACATCTAATAATTAT[A/G]GAGAGTCCTTACCAT | 55632 |
rs750217036 | snp | A/G | 3.67141e-05 | 0.00428435 | intron-variant | G2E3 | GRCh38.p7 | 14:30605861 | TATCACATGTATAGA[A/G]AAAGAGATAGATAGC | 55632 |
rs750263322 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30559818 | AAATGCCTGAGTGGG[A/G]TTTAAACTGAAATTC | 55632 |
rs750271090 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30561781 | AAACTGTGTATGTTC[A/G]GTGAGTACTTATTAT | 55632 |
rs750296264 | in-del | -/TG | | | intron-variant | G2E3 | GRCh38.p7 | 14:30573411 | AAACAACAGGATATG[-/TG]TGTGTGTGTGTGTGT | 55632 |
rs750300605 | snp | G/T | 1.66532e-05 | 0.00288554 | missense, intron-variant | G2E3 | GRCh38.p7 | 14:30605682 | AGTAGCATATGTTAT[G/T]GAAAATGATAATTTT | 55632 |
rs750301827 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30591547 | AAGGGAGAATTGATT[C/G]CATGCTTCTCCCCTA | 55632 |
rs750364805 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30605054 | GGCATACGCCACGAC[A/G]CCCAGCTTATTTTGT | 55632 |
rs750382422 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30574788 | GCACAATATTTTATC[A/G]TGTATTTGTACCCTA | 55632 |
rs750385637 | in-del | -/AT | | | intron-variant | G2E3 | GRCh38.p7 | 14:30583403 | AAATGGAGTCATAAA[-/AT]GCACTAGTGAAGTAA | 55632 |
rs750423899 | snp | A/G | 1.77801e-05 | 0.00298157 | utr-variant-5-prime, missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30586795 | GAGAAATGGAATCTC[A/G]CTGTACATTACTACT | 55632 |
rs750448018 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30596640 | AGACTTAGGTACTCC[C/T]TCTTGTTTCTTTCAT | 55632 |
rs750460695 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30574285 | CTTAGCATAAATACA[A/G]TACTTTCAACTAAAT | 55632 |
rs750508147 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30566566 | GAAATACAACTGATA[C/T]TTGTGTGTTGATCTT | 55632 |
rs750570258 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30611066 | CTCTCATTATCGTGT[A/C]ACACTTAGCATTATT | 55632 |
rs750612057 | snp | G/T | 0.00647551 | 0.0565316 | intron-variant | G2E3 | GRCh38.p7 | 14:30612187 | TGAGTAAAGTGGCTG[G/T]ATTTTCTCCTTCATT | 55632 |
rs750621037 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30610319 | TGTATTATAATGCTA[A/C]ATAAAACAGAATATG | 55632 |
rs750705822 | snp | C/T | 1.76446e-05 | 0.00297018 | intron-variant | G2E3 | GRCh38.p7 | 14:30608078 | AATCAGGGTAAGCAA[C/T]GTATCTGTTTATTAA | 55632 |
rs750747087 | snp | A/G | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30576993 | GCACTTTGGGAGGCA[A/G]AGGCAGGCGGATCAT | 55632 |
rs750853531 | in-del | -/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30574425 | TCTTTTTTTTTTAAC[-/T]TTTTTTTTTTTTTAG | 55632 |
rs750866172 | snp | A/G | 1.69029e-05 | 0.00290709 | intron-variant | G2E3 | GRCh38.p7 | 14:30589511 | ATTTTACTATTAAGT[A/G]ATGTCATAAATATTG | 55632 |
rs750888457 | snp | C/T | | | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30559027 | ACAGCCAGGTTAGCA[C/T]CGAGCAGCAGCGCAG | 55632 |
rs750932961 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30587605 | TGAGATGTCAGATTA[C/T]AGCTGAAGACTTTAC | 55632 |
rs750943671 | in-del | -/AGAAT | | | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30618056 | TATTTTTTAAGTAAC[-/AGAAT]AGATTTGAAAGAGAT | 55632 |
rs750960540 | snp | A/G/T | 5.01268e-05 | 0.00500613 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616298 | AAATCTACAACAACA[A/G/T]TGGAAGACATTCTTA | 55632 |
rs751014955 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30602930 | TTTTGATGTTATAAT[C/T]ATTGTTTGCCTGTTT | 55632 |
rs751025509 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30589225 | CAATGTAAGTAGCCT[C/T]TTACTTTGACCATGA | 55632 |
rs751043877 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30561568 | TACTAGAATTCTCCA[A/T]ATCTATCTCTTATTA | 55632 |
rs751077382 | snp | A/G | | | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30559047 | CAGCAGCGCAGGAGC[A/G]CCAGAAGGGCGGGAG | 55632 |
rs751082025 | snp | G/T | | | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558245 | CAAAGGCTAAAGGTA[G/T]GCTGTCATGGTTTGG | 55632 |
rs751130624 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30571543 | TGAAGATTCTTCACT[A/G]TGTTTTCTTCTAGAA | 55632 |
rs751138194 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30600938 | ATATGAACACAGAGA[G/T]AACTGGACCTGGAGC | 55632 |
rs751193588 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616704 | TTAGGCTAAAAAAAG[A/G]TTTTTTTTGTTAAAG | 55632 |
rs751199282 | snp | C/T | 1.66668e-05 | 0.00288672 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616314 | TGGAAGACATTCTTA[C/T]TTTTGCAACTGGTTG | 55632 |
rs751202833 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30570474 | TCCTATTAAGCATAT[A/G]TTGGTATACTTGATG | 55632 |
rs751276811 | snp | C/G | | | utr-variant-5-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30559213 | GTCGGCGTGCCCCGA[C/G]GTACAGCGGGCCGGG | 55632 |
rs751287195 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30582687 | GGTGTAGAATGTCCA[A/G]TATGAACAAATGGCA | 55632 |
rs751289279 | snp | A/C | 0.00062525 | 0.0176701 | intron-variant | G2E3 | GRCh38.p7 | 14:30615561 | GGATATTTTATTTTA[A/C]TTTTAACGATCTCAG | 55632 |
rs751316268 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30615176 | GTATATCCATATCTT[C/T]TCTTTTTCCTCACAT | 55632 |
rs751344633 | snp | A/C | 1.67528e-05 | 0.00289415 | intron-variant | G2E3 | GRCh38.p7 | 14:30597560 | TATGATAAAAAAAAG[A/C]TATTTTAAATGTAGG | 55632 |
rs751355614 | in-del | -/A | 0.0106255 | 0.07211 | frameshift-variant, intron-variant | G2E3 | GRCh38.p7 | 14:30605566 | TTAGGATTCCAAATT[-/A]AAAAAAAAACTAAAA | 55632 |
rs751409756 | in-del | -/GGGGGTACATGTGAAGGTTTGTTACATAGGTAAACA | | | intron-variant | G2E3 | GRCh38.p7 | 14:30574445 | TTTTTTTTTAGGTTT[lengthTooLong]ACATGTCATGGGGGT | 55632 |
rs751432920 | snp | A/T | 1.65373e-05 | 0.00287548 | intron-variant | G2E3 | GRCh38.p7 | 14:30597381 | CACCTGATAACAGAT[A/T]TAAATCATTAACAGT | 55632 |
rs751459017 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30593832 | GTATACAATTAACAT[G/T]CAATAAATACTTCAG | 55632 |
rs751461432 | snp | A/G | | | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30602107 | CCAGACAGTCACCTG[A/G]ATCCCAGAGTAAAGA | 55632 |
rs751486300 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30608737 | GACAATGCAAGCCAT[G/T]TAACTTTTCTTCCTT | 55632 |
rs751506010 | in-del | -/GT | | | intron-variant | G2E3 | GRCh38.p7 | 14:30603190 | AATTAGCTGGGCATA[-/GT]GTTGTGCATCTGTAG | 55632 |
rs751508152 | snp | G/T | | | missense, intron-variant | G2E3 | GRCh38.p7 | 14:30605505 | ATTCATGTTTTATAG[G/T]CAAGGCAGCAAATTT | 55632 |
rs751525559 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30573434 | GTGTGTGTGTGTGCG[G/T]GTGTGTGTGTCTCTG | 55632 |
rs751539279 | snp | C/T | 3.80974e-05 | 0.00436432 | intron-variant | G2E3 | GRCh38.p7 | 14:30607850 | GTTATCTTATAATAA[C/T]AGAAGTGTATTTGAT | 55632 |
rs751572242 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30585646 | ATCTTTAAAAAGAAC[C/T]AACTTTTTTTTTTTA | 55632 |
rs751649573 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | G2E3 | GRCh38.p7 | 14:30619897 | AGATTAAGATTCTGA[C/T]GAAACTGAAAGATAC | 55632 |
rs751652243 | in-del | -/A | 0.000300827 | 0.0122606 | intron-variant | G2E3 | GRCh38.p7 | 14:30597550 | ATTTAGCCTTATGAT[-/A]AAAAAAAAGATATTT | 55632 |
rs751673838 | snp | A/G | 3.88734e-05 | 0.00440854 | intron-variant | G2E3 | GRCh38.p7 | 14:30586698 | TATATTTTTATATCT[A/G]TTTACTTTTTCACTG | 55632 |
rs751697009 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30584656 | TTAAGCATCTTTTAA[G/T]GTGTTTAATGGCTCT | 55632 |
rs751755290 | snp | A/C | 1.65919e-05 | 0.00288022 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30612336 | TTAGTAAAAGACATA[A/C]TTGGCTACCATGTAA | 55632 |
rs751775037 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30596923 | GTTTCCTTCTGAGTA[C/T]CCTCTGTCTGGTGCT | 55632 |
rs751853881 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30567927 | GATTTCAGTCTTGTA[A/C]AATGTATTATTTTGT | 55632 |
rs751924171 | snp | A/T | 3.31631e-05 | 0.00407191 | synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30612209 | TCCTTCATTACAGAT[A/T]AATACTGCAACAACT | 55632 |
rs752067072 | snp | C/T | 1.71179e-05 | 0.00292552 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30592425 | CAGAGAGAATGTATT[C/T]TCCAGTTTACTGGCA | 55632 |
rs752143201 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30591220 | GGTTGGCAGGTATTC[C/T]CCAGTGACCTAGGTG | 55632 |
rs752161879 | snp | A/C | 4.63017e-05 | 0.00481131 | synonymous-codon, intron-variant | G2E3 | GRCh38.p7 | 14:30605532 | ATTTAGAAGAAATGT[A/C]TCAACACTATTAATA | 55632 |
rs752191772 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30578732 | AATTCATGTGTATGG[A/G]TGGATTTATGATATG | 55632 |
rs752244691 | snp | C/T | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30576037 | AAAATTCATGTGGAA[C/T]GAAAAAAGAGCACAA | 55632 |
rs752250010 | snp | C/T | 1.75696e-05 | 0.00296386 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30592447 | TTACTGGCAATTTTG[C/T]GTGAGTTATTTAACT | 55632 |
rs752308338 | in-del | -/G | | | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558241 | TTGACAAAGGCTAAA[-/G]GTATGCTGTCATGGT | 55632 |
rs752331668 | snp | A/G | 2.22195e-05 | 0.00333306 | synonymous-codon, intron-variant | G2E3 | GRCh38.p7 | 14:30605541 | AAATGTATCAACACT[A/G]TTAATAGAGTTAGGA | 55632 |
rs752365709 | in-del | -/TGC | | | intron-variant | G2E3 | GRCh38.p7 | 14:30604585 | GTTCTGGGGTAATGC[-/TGC]TGCTGCTGCTGCTGC | 55632 |
rs752391136 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30618375 | TTTGTTTCTTTATCC[A/G]CCTTATTTTTATTAC | 55632 |
rs752408347 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30582375 | AAAATAATCTACTTA[A/T]AAAAATGCATGCCTG | 55632 |
rs752418585 | snp | A/C | 1.67094e-05 | 0.0028904 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616515 | AAAAGGAAGAAAGTT[A/C]TCATTACATTGGACA | 55632 |
rs752421739 | snp | A/C | 3.44133e-05 | 0.00414795 | intron-variant | G2E3 | GRCh38.p7 | 14:30602166 | GAAATACATAAAAAT[A/C]TATTTGGAGAAAATT | 55632 |
rs752476759 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30571670 | ACTATTTATTGAATA[A/G]ACTACCATTTGAATA | 55632 |
rs752547033 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616907 | GAATGCCACAATTTC[G/T]CTAGGTTTATTCAAT | 55632 |
rs752595009 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30582849 | GTAGTTAGGCTATTT[C/T]ACTATATTAAATACG | 55632 |
rs752625721 | in-del | -/CA | 3.33634e-05 | 0.00408418 | intron-variant | G2E3 | GRCh38.p7 | 14:30605842 | TATTGTTGTATATAC[-/CA]AATATCACATGTATA | 55632 |
rs752648443 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30581862 | TGCTACAATGAAATA[G/T]GAGGAATTTAAATGA | 55632 |
rs752673394 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30607210 | TAAGTGGATAAAGCA[G/T]AAGTCAAACTTTTTA | 55632 |
rs752702556 | snp | A/G | 1.69447e-05 | 0.00291068 | intron-variant | G2E3 | GRCh38.p7 | 14:30597574 | GATATTTTAAATGTA[A/G]GATTTAATAGCAATG | 55632 |
rs752703523 | snp | A/C | 1.73045e-05 | 0.00294142 | intron-variant | G2E3 | GRCh38.p7 | 14:30612166 | TGCATGTCACTCAAA[A/C]GTAAATGAGTAAAGT | 55632 |
rs752709057 | snp | C/T | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30575965 | AATTTACAGATTCAC[C/T]GCTATTCCTGTCAAA | 55632 |
rs752822477 | snp | G/T | 2.44496e-05 | 0.00349631 | intron-variant | G2E3 | GRCh38.p7 | 14:30586834 | AGTATAATTTATAAT[G/T]AAATTCTAGAAATTT | 55632 |
rs752865970 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30593196 | AATGTATATACTGTA[C/T]TGCTGACAATATTAC | 55632 |
rs752912356 | snp | A/C | 3.29837e-05 | 0.00406088 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30601868 | ATTGGGAGTGTTTGG[A/C]ATGTAGGGGTATTAT | 55632 |
rs753054358 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30598489 | CTTTTATAGAGATGC[C/T]TCCTGGGAATTAGAG | 55632 |
rs753055591 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30568016 | TTCTGTTGTAGGGTG[C/G]AGTGTTCTGTATATG | 55632 |
rs753072075 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30597122 | CATTTTAAAGGGCAA[C/G]ACAACATTTAGTAAC | 55632 |
rs753103161 | snp | A/T | 1.64904e-05 | 0.00287139 | intron-variant | G2E3 | GRCh38.p7 | 14:30601734 | GAAACTAGAATAATA[A/T]CAAAATGTAAGTTCT | 55632 |
rs753174058 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30579618 | AGCAGTTTGTATTTG[C/T]GGTTTTCACTCTTTG | 55632 |
rs753236985 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30611514 | TCTTGCACATAAATG[A/G]CCAAGTATTTCTTTG | 55632 |
rs753270402 | snp | C/T | 1.73833e-05 | 0.00294811 | intron-variant | G2E3 | GRCh38.p7 | 14:30593671 | GTAAGCTTTCTCTGA[C/T]TGATATAAAATTATG | 55632 |
rs753274414 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30610527 | AGGCTCGCTTGAGCC[C/T]GGGAGGCAGAGGTGG | 55632 |
rs753281704 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30580541 | GCACAAATACGAATG[A/G]CATGGCTATTGATGA | 55632 |
rs753344576 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30612879 | TGAAAAAAGAATTGT[A/G]TAAATGTATGATGCT | 55632 |
rs753400527 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30579808 | AACTATAAATGAGAT[G/T]ATATTTACCTAGTGG | 55632 |
rs753435442 | in-del | -/ATAAG | | | intron-variant | G2E3 | GRCh38.p7 | 14:30581322 | ATTTGTTTTATGTAT[-/ATAAG]ATATGGTTCGTATCT | 55632 |
rs753546004 | snp | A/G | 2.17365e-05 | 0.00329663 | missense, intron-variant | G2E3 | GRCh38.p7 | 14:30605548 | TCAACACTATTAATA[A/G]AGTTAGGATTCCAAA | 55632 |
rs753564417 | snp | C/G | | | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558368 | TAGCGCCCCTCACCC[C/G]CTAGCATTTCCAGTC | 55632 |
rs753569004 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30574655 | CATTTAGCTCCCACT[G/T]ACAAGTGAGAACATG | 55632 |
rs753679051 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30560521 | TAGGATAGTTAAAAT[A/G]TGAGCATTTTTCATA | 55632 |
rs753682707 | snp | A/G | 8.20378e-05 | 0.00640408 | intron-variant | G2E3 | GRCh38.p7 | 14:30586671 | CCATAGGGTTTTTTT[A/G]AAATATTTAAATATA | 55632 |
rs753688023 | snp | C/T | 1.68545e-05 | 0.00290292 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616540 | TGGACATTAAAATGT[C/T]TCCTTGAACAAAGAG | 55632 |
rs753691103 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | G2E3 | GRCh38.p7 | 14:30619710 | CCTACACTATGCCAG[A/G]TATTATGCTAGGTGA | 55632 |
rs753706666 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30574637 | GTGTTCATGAGTTCT[C/T]ATCATTTAGCTCCCA | 55632 |
rs753712299 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30573171 | TTTATTATTTCCTAG[A/G]ATGTAAATAATTGAT | 55632 |
rs753725823 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30598025 | AAATAACACTAATGG[A/G]TTTATATCTTAAAGA | 55632 |
rs753827825 | in-del | -/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30594779 | AGTTTGACTGATACC[-/T]TTTTTTTTTTTTGTA | 55632 |
rs753861155 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30565823 | CCCACCACCACACCC[A/G]GCTAATTTTTTTGTA | 55632 |
rs753864817 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30608832 | ATTAAAAGCATAGGC[C/T]TTAGCCAGGCGTGGT | 55632 |
rs753865862 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30610189 | ACTATGTATTCTGTA[C/G]TGTTTTGTTACTAAA | 55632 |
rs753866355 | snp | C/T | 0.000214754 | 0.0103601 | intron-variant | G2E3 | GRCh38.p7 | 14:30560731 | AATTTATTGTGTATA[C/T]ACTACCTTGAAGGAT | 55632 |
rs753871797 | snp | C/G/T | 3.29507e-05 | 0.00405887 | intron-variant | G2E3 | GRCh38.p7 | 14:30598624 | AAAGTTCAGTTGTGC[C/G/T]TAGTGGTTCCTTGTT | 55632 |
rs753918247 | snp | G/T | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30576919 | CTTTTTCAGTAAGAT[G/T]AGGCACTTTAGAAAA | 55632 |
rs753936869 | snp | A/T | 1.70909e-05 | 0.00292321 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30608047 | ATGTTTCAGACTTTG[A/T]TGTGGCACAGATTAT | 55632 |
rs753958561 | in-del | -/TTTCTTTTTC | | | intron-variant | G2E3 | GRCh38.p7 | 14:30589114 | CCTTCTTTCCTATCT[-/TTTCTTTTTC]TTTCTTTTTCTTTCT | 55632 |
rs753999832 | in-del | -/TG | 0.000133118 | 0.00815729 | intron-variant | G2E3 | GRCh38.p7 | 14:30581126 | ACCTTGGTAAGTAAC[-/TG]TATTTAAAATAATTT | 55632 |
rs754085603 | snp | A/G | 0.000297969 | 0.0122023 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30602113 | AGTCACCTGGATCCC[A/G]GAGTAAAGATCTACT | 55632 |
rs754110380 | snp | G/T | 1.68261e-05 | 0.00290048 | intron-variant | G2E3 | GRCh38.p7 | 14:30589503 | AGTAAATTATTTTAC[G/T]ATTAAGTAATGTCAT | 55632 |
rs754124984 | snp | A/G | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30576157 | AACAGCATAGTACTG[A/G]TACAAAAACAGGCAC | 55632 |
rs754138572 | snp | C/G | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30577028 | TCAAGAGATTAAGAC[C/G]ATCCTGGCCAACATG | 55632 |
rs754140540 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30588828 | ATGAAGCTTAAGTCA[A/G]ATTTTTAAAAAGTCA | 55632 |
rs754195509 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30587346 | CCCTTTGTTCCCCCT[C/T]CCCTCCACCAATTTC | 55632 |
rs754196200 | snp | A/G | 3.3222e-05 | 0.00407553 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30602017 | AGTTCCAAAAAGCCA[A/G]AAAACATGTATTACC | 55632 |
rs754198384 | snp | A/G | 2.75706e-05 | 0.00371275 | intron-variant | G2E3 | GRCh38.p7 | 14:30586845 | TAATTAAATTCTAGA[A/G]ATTTGGTGTTCTAAA | 55632 |
rs754213171 | snp | A/G | | | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30557823 | AAAAACAGTACATCA[A/G]TTAATAGCTTTACAC | 55632 |
rs754277096 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30614551 | GACCTACTCACCTCT[G/T]AAGGACCCTATCTCC | 55632 |
rs754278638 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30567165 | CTTTTTCTGGCTTTG[G/T]TATCGGGGTATTGGT | 55632 |
rs754285953 | snp | G/T | 1.65466e-05 | 0.00287628 | intron-variant | G2E3 | GRCh38.p7 | 14:30601899 | CTACAATTCAGGTAA[G/T]TTTTTTGTAATTTTG | 55632 |
rs754313153 | snp | A/G | 1.64977e-05 | 0.00287203 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30615480 | AGCTTTTTACAGTAC[A/G]CACATTACCTGATGT | 55632 |
rs754318193 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30599473 | ACCTCGTGATCTGCC[C/T]GCCTCGGCCTCCCAA | 55632 |
rs754332107 | snp | C/T | 1.71929e-05 | 0.00293192 | synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30615361 | AAGTTTTAAGCAGGG[C/T]CTGAAAACCCTTGGT | 55632 |
rs754371254 | snp | A/G | | | synonymous-codon, intron-variant, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30598591 | GCGAGACTATAATGC[A/G]CCTGATAGGTATTTC | 55632 |
rs754486521 | in-del | -/GT | | | intron-variant | G2E3 | GRCh38.p7 | 14:30573439 | TGTGTGTGCGTGTGT[-/GT]GTGTCTCTGTGTGTG | 55632 |
rs754560369 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30601021 | AGAGACACACACATA[C/G]ACAGGACAGAAATTA | 55632 |
rs754575998 | snp | A/C | 1.71111e-05 | 0.00292494 | intron-variant | G2E3 | GRCh38.p7 | 14:30602161 | TTGGAGAAATACATA[A/C]AAATCTATTTGGAGA | 55632 |
rs754647761 | snp | C/T | | | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558277 | TTGTACTGATCCGTT[C/T]AGGTAATTCAATGTT | 55632 |
rs754699231 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30570490 | TTGGTATACTTGATG[A/G]TGTCTCATAGTCTCT | 55632 |
rs754726906 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30610528 | GGCTCGCTTGAGCCC[A/G]GGAGGCAGAGGTGGC | 55632 |
rs754753838 | snp | G/T | 3.48377e-05 | 0.00417345 | intron-variant | G2E3 | GRCh38.p7 | 14:30615563 | ATATTTTATTTTACT[G/T]TTAACGATCTCAGAA | 55632 |
rs754776023 | in-del | -/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30587773 | CTGGCTTCTCCCAAA[-/G]CAAGTGATGAGAGAG | 55632 |
rs754829148 | in-del | -/ATGTTGGG | | | intron-variant | G2E3 | GRCh38.p7 | 14:30603410 | AATTACATCTTTATA[-/ATGTTGGG]TATTTGTTCAGCTGT | 55632 |
rs754868758 | snp | C/T | 5.0336e-05 | 0.00501652 | intron-variant | G2E3 | GRCh38.p7 | 14:30597563 | GATAAAAAAAAGATA[C/T]TTTAAATGTAGGATT | 55632 |
rs754920776 | in-del | -/TT | 1.67427e-05 | 0.00289328 | intron-variant | G2E3 | GRCh38.p7 | 14:30589343 | TTAATGCCCAACTAG[-/TT]TCTTAGAGTTTATTT | 55632 |
rs754923396 | snp | C/T | 1.65353e-05 | 0.00287531 | intron-variant | G2E3 | GRCh38.p7 | 14:30597386 | GATAACAGATTTAAA[C/T]CATTAACAGTAGACT | 55632 |
rs754926042 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30608751 | TTTAACTTTTCTTCC[G/T]TAACCTCCCTCCTAC | 55632 |
rs754962984 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30580905 | AAATGTTCCCGACTC[G/T]TAACACCCCAGTTGA | 55632 |
rs755045418 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30560788 | TTCAGATCTCAGATT[C/T]TGAATCAGTAGGTCT | 55632 |
rs755057513 | snp | A/T | | | utr-variant-3-prime, downstream-variant-500B | G2E3 | GRCh38.p7 | 14:30619921 | AAGATACAAGATTCC[A/T]TTACTCTCCACATTT | 55632 |
rs755072579 | in-del | -/A | | | intron-variant | G2E3 | GRCh38.p7 | 14:30589218 | ATCAAACAATGTAAG[-/A]TAGCCTCTTACTTTG | 55632 |
rs755106684 | snp | C/T | 1.70012e-05 | 0.00291553 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616574 | CTTCTTTAAAAGCTG[C/T]TATTGATAACTCTCT | 55632 |
rs755107687 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30618836 | TCTTTTCTTATTAAT[G/T]TTATAACCAGTGCAT | 55632 |
rs755173653 | snp | A/T | 6.84112e-05 | 0.00584815 | intron-variant | G2E3 | GRCh38.p7 | 14:30586700 | TATTTTTATATCTAT[A/T]TACTTTTTCACTGTT | 55632 |
rs755191005 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30584664 | CTTTTAATGTGTTTA[A/G]TGGCTCTTTGTATAT | 55632 |
rs755205789 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30597009 | GGGAAGAAAGCTGTC[A/T]TAGAGATTGAGTTAA | 55632 |
rs755243992 | snp | C/T | 1.64754e-05 | 0.00287009 | intron-variant | G2E3 | GRCh38.p7 | 14:30598645 | GTTCCTTGTTTAAAC[C/T]TTCTGCTGAGAAAGT | 55632 |
rs755261450 | snp | G/T | 0.000375869 | 0.0137038 | intron-variant | G2E3 | GRCh38.p7 | 14:30560822 | GGATGGCATTGAACA[G/T]TCTGCATATTTAACT | 55632 |
rs755275628 | in-del | -/A | | | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30557642 | AAACAAGGATACTAC[-/A]GTCCTTCTTAAACTT | 55632 |
rs755375447 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30562352 | TATTATAATAATCCT[C/T]GCTCTACAATCATAA | 55632 |
rs755408639 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30566893 | TGTTTTTATCATCAA[G/T]GAGTTGTATTTTGTC | 55632 |
rs755412021 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30591674 | CTGTGTCTTAAATCT[C/T]CCTCTCCTTTCTCTT | 55632 |
rs755446876 | snp | C/G | 1.7179e-05 | 0.00293074 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30592428 | AGAGAATGTATTTTC[C/G]AGTTTACTGGCAATT | 55632 |
rs755477670 | snp | A/G | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30577118 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 55632 |
rs755521588 | in-del | -/TTG | | | upstream-variant-2KB, intron-variant | SCFD1, G2E3 | GRCh38.p7 | 14:30620500 | TAGGGCAGAAATAAT[-/TTG]TTTAGTTGGAACACA | 55632 |
rs755627909 | in-del | -/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30559305 | GGGAAGACGCAGAAC[-/G]TTCCAGAGAGAGAAG | 55632 |
rs755642190 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30578745 | GGATGGATTTATGAT[A/G]TGTTGAATTCATCAC | 55632 |
rs755695670 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30590737 | AAAGGTGAGCATGAA[C/T]CTAAGGACTACGTGA | 55632 |
rs755706911 | snp | C/T | 2.21781e-05 | 0.00332995 | synonymous-codon, intron-variant | G2E3 | GRCh38.p7 | 14:30605542 | AATGTATCAACACTA[C/T]TAATAGAGTTAGGAT | 55632 |
rs755709373 | in-del | -/TCTTTTAGTTTTTTTTTT | 2.89624e-05 | 0.00380531 | intron-variant | G2E3 | GRCh38.p7 | 14:30605843 | TTGTTGTATATACCA[-/TCTTTTAGTTTTTTTTTT]AATATCACATGTATA | 55632 |
rs755725372 | snp | C/G | 1.78774e-05 | 0.00298971 | intron-variant | G2E3 | GRCh38.p7 | 14:30592461 | GCGTGAGTTATTTAA[C/G]TGTTAAATATGAAAG | 55632 |
rs755774106 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30606206 | TCCTGGTCCACATGT[A/G]ACCAATTTTTCAGTA | 55632 |
rs755794844 | snp | A/G | 1.67525e-05 | 0.00289413 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616523 | GAAAGTTCTCATTAC[A/G]TTGGACATTAAAATG | 55632 |
rs755831356 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30601459 | TAAGCATAGTCATCT[C/T]TAAGTAGAAAGGAAA | 55632 |
rs755845152 | snp | A/G | 1.65015e-05 | 0.00287237 | synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30592343 | CTGTGTTTGCAAGAA[A/G]AATGGTGCTTCAATT | 55632 |
rs755850222 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30603000 | TAGAAAGTTTAAGGC[A/G]TACATACTATTATCA | 55632 |
rs755899530 | snp | G/T | 3.46063e-05 | 0.00415956 | intron-variant | G2E3 | GRCh38.p7 | 14:30602171 | ACATAAAAATCTATT[G/T]GGAGAAAATTATGAT | 55632 |
rs755904762 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30618469 | TTAATTTCCCCTAGG[G/T]TAGAAATTAAAGCTG | 55632 |
rs755912932 | in-del | -/AA | | | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30618219 | TTAAGAACATTAAAC[-/AA]GACATTTCTTTGGCT | 55632 |
rs755952451 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616951 | CTCATTTTATTTTAA[A/G]GCATTAAATAGAAAA | 55632 |
rs755988824 | snp | A/C | 3.32712e-05 | 0.00407854 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616374 | CCACTCCTTCAATTG[A/C]GTGTCTGCATGTGGA | 55632 |
rs756050837 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30595319 | ATTTGTTTTAATTAA[A/G]GGTTTGTATTTGGAT | 55632 |
rs756089935 | snp | C/G | 1.64757e-05 | 0.00287012 | missense, intron-variant, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30598529 | TATCAAGAGCTTCTG[C/G]AGCACTATGAGCGTT | 55632 |
rs756108126 | snp | C/G/T | 7.15007e-05 | 0.00597881 | intron-variant | G2E3 | GRCh38.p7 | 14:30607856 | TTATAATAATAGAAG[C/G/T]GTATTTGATATATTT | 55632 |
rs756210847 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30614732 | AGGCAAAAATGATAT[A/G]TTTGTTCTTTGCTTA | 55632 |
rs756288052 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30575211 | TATGCCTGTTGGTCG[C/T]GTATATGTCTTCTTT | 55632 |
rs756337505 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30585933 | TAGATTCTCCAGTTA[C/T]TATGCAGAAGGTTTT | 55632 |
rs756361590 | snp | C/T | | | downstream-variant-500B | G2E3 | GRCh38.p7 | 14:30620190 | GCCTTACAAGGGCTA[C/T]TTGTCTATGGTTGCT | 55632 |
rs756373382 | snp | A/G | 1.65677e-05 | 0.00287812 | intron-variant | G2E3 | GRCh38.p7 | 14:30586836 | TATAATTTATAATTA[A/G]ATTCTAGAAATTTGG | 55632 |
rs756464801 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30574321 | TTTGGTCAATTGCCT[C/T]GGTGATGTCCTTTGG | 55632 |
rs756492198 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30560500 | TAGACTTAAATACTC[A/G]GTGTTTAGGATAGTT | 55632 |
rs756509210 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30586474 | TGTCATTTTCAGTGA[C/T]GTTACTTCATAAATT | 55632 |
rs756511423 | snp | A/C | 1.64876e-05 | 0.00287116 | intron-variant | G2E3 | GRCh38.p7 | 14:30601738 | CTAGAATAATAACAA[A/C]ATGTAAGTTCTGCTT | 55632 |
rs756513514 | snp | A/G | 9.56526e-05 | 0.00691499 | intron-variant | G2E3 | GRCh38.p7 | 14:30615332 | GAATGTTGGCTCATT[A/G]TTTTTCTTCTCTTAA | 55632 |
rs756621294 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30567008 | CCATATGCTGAACCA[C/T]CTTTGCATTTCTGGG | 55632 |
rs756650742 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30579700 | AGTACCATGGTGTAA[A/C]CTGCAGTCACTCAGT | 55632 |
rs756690349 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30613206 | CACCATCCAGATCTA[A/G]CACTTATTAACTTGT | 55632 |
rs756694722 | in-del | -/TTCT | | | intron-variant | G2E3 | GRCh38.p7 | 14:30573201 | TTCATGAAAAAAAAA[-/TTCT]AATAGCTTTTGACCT | 55632 |
rs756701000 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30588914 | ATGTTAACTAGGGTT[C/T]AATAGGTTTTCTTGT | 55632 |
rs756776742 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30580549 | ACGAATGGCATGGCT[A/G]TTGATGATGTGATTT | 55632 |
rs756870349 | snp | A/C | 1.81141e-05 | 0.00300944 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30593488 | GGTCATTTTGTTGGG[A/C]CCATCGACCTGTTCA | 55632 |
rs756895081 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30579809 | ACTATAAATGAGATT[A/G]TATTTACCTAGTGGC | 55632 |
rs756908676 | snp | C/G | | | utr-variant-5-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30559236 | GGGCCGGGAAAAGTG[C/G]CACTGAGGCTCTGGA | 55632 |
rs756916088 | in-del | -/TT | 1.82917e-05 | 0.00302416 | intron-variant | G2E3 | GRCh38.p7 | 14:30615344 | ATTATTTTTCTTCTC[-/TT]AAGTTTTAAGCAGGG | 55632 |
rs756979730 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30591441 | AGGGCTGCCATAGCA[A/C]ATTGGCTGCTTAAAA | 55632 |
rs757015135 | in-del | -/TCGTTT | | | cds-indel, downstream-variant-500B | G2E3 | GRCh38.p7 | 14:30619726 | TATTATGCTAGGTGA[-/TCGTTT]ATATGTCAGCCTATT | 55632 |
rs757031778 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30590800 | CCTAAACTTCCTGGT[A/G]ATAGTGAGCTTGTGG | 55632 |
rs757034772 | snp | C/T | 1.79255e-05 | 0.00299373 | intron-variant | G2E3 | GRCh38.p7 | 14:30592464 | TGAGTTATTTAACTG[C/T]TAAATATGAAAGTTC | 55632 |
rs757083000 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30603526 | AATTAGTCGCTAAGC[A/G]TGATGAAATACTTTC | 55632 |
rs757104750 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30605015 | GATTCTCCTGCCTCA[G/T]CCTCCTGAGTAGCTG | 55632 |
rs757118525 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30560589 | TAAGCCTTTCTGCTC[A/G]TTTCATATGTGCTGT | 55632 |
rs757123296 | snp | A/G | 4.22851e-05 | 0.00459791 | missense, intron-variant | G2E3 | GRCh38.p7 | 14:30605555 | TATTAATAGAGTTAG[A/G]ATTCCAAATTAAAAA | 55632 |
rs757124178 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30605886 | GATAGCTGGTTAGAA[C/T]TGATATTTAATACCT | 55632 |
rs757125754 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30573208 | AAAAAAAATTCTAAT[A/G]GCTTTTGACCTCTAC | 55632 |
rs757177542 | snp | G/T | 1.68584e-05 | 0.00290326 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616541 | GGACATTAAAATGTT[G/T]CCTTGAACAAAGAGA | 55632 |
rs757202467 | snp | A/G/T | | | utr-variant-3-prime, downstream-variant-500B | G2E3 | GRCh38.p7 | 14:30619800 | GTGACATTTATAACA[A/G/T]TGTTTTATAAATAAA | 55632 |
rs757228477 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30584236 | TGCTGAATAATATTC[C/T]ATCATATGGGCATAC | 55632 |
rs757250239 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30570344 | AGCTTCTTAAAAATG[C/T]GTAGATTGAAGTCTT | 55632 |
rs757284774 | in-del | -/TAACCCAGTAG | | | intron-variant | G2E3 | GRCh38.p7 | 14:30560164 | ATATGGAACTCTGTC[-/TAACCCAGTAG]TAAAGTCATGCCTTC | 55632 |
rs757360122 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30565825 | CACCACCACACCCGG[A/C]TAATTTTTTTGTATT | 55632 |
rs757385016 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30594254 | AAAAGATTCCAGTTA[C/T]TAGTAACATCAAATA | 55632 |
rs757410880 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30563915 | GTAGAGACAGGGTTT[C/T]GCCATGTTGGTCAGG | 55632 |
rs757464178 | snp | C/T | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30576250 | CTTTGACAAAGATGA[C/T]AAAAAACAAGCAATA | 55632 |
rs757484785 | snp | A/G | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30576955 | GATGGGGCCAGGCAC[A/G]ATGGCTCACACCTGT | 55632 |
rs757571738 | snp | C/T | 1.68394e-05 | 0.00290162 | intron-variant | G2E3 | GRCh38.p7 | 14:30589505 | TAAATTATTTTACTA[C/T]TAAGTAATGTCATAA | 55632 |
rs757590347 | in-del | -/TTCA | | | intron-variant | G2E3 | GRCh38.p7 | 14:30604876 | TTTGAGCTTGCTTCA[-/TTCA]TTCATTCATTCATTC | 55632 |
rs757609058 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30597756 | TAAGTAGCTCAGCTA[C/T]GTCCAATTTTAATTG | 55632 |
rs757655708 | snp | G/T | 1.65795e-05 | 0.00287914 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30602025 | AAAGCCAAAAAACAT[G/T]TATTACCCAATTCTA | 55632 |
rs757659988 | snp | A/G | 2.92856e-05 | 0.00382648 | intron-variant | G2E3 | GRCh38.p7 | 14:30586850 | AAATTCTAGAAATTT[A/G]GTGTTCTAAAGAAGA | 55632 |
rs757665559 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30575370 | TACATATTGAGGGAA[C/G]ATACCTCAAAATAAT | 55632 |
rs757723557 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30585901 | TGTGTACATCTCTGG[C/G]CATGCATGTGGACTT | 55632 |
rs757747433 | snp | A/T | 3.32906e-05 | 0.00407973 | intron-variant | G2E3 | GRCh38.p7 | 14:30601915 | TTTTTTGTAATTTTG[A/T]ATAAAGTTTTTATTC | 55632 |
rs757850764 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30570421 | TATTATTTCTTCAAA[C/G]ATTCTTTCTGTTCCA | 55632 |
rs757881366 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30599981 | GCTCTTTTCTACAAC[A/T]GTCATTTTGTGCATT | 55632 |
rs757882045 | snp | A/G | 1.65455e-05 | 0.00287619 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30602040 | GTATTACCCAATTCT[A/G]ATAATGTGGGGATTA | 55632 |
rs757891553 | snp | A/C | 1.69112e-05 | 0.0029078 | intron-variant | G2E3 | GRCh38.p7 | 14:30601937 | TTTTTATTCAAATGT[A/C]TATGATTTAAAAGTT | 55632 |
rs757893310 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30598633 | TTGTGCTTAGTGGTT[A/C]CTTGTTTAAACCTTC | 55632 |
rs757896562 | snp | C/G | | | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30559068 | AGGGCGGGAGCACAC[C/G]GGCCCTTCCCCACAG | 55632 |
rs757990738 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30615077 | GTTAGTTTTGAAACT[A/G]TAAAGCCAAATAATG | 55632 |
rs758028320 | snp | A/C | 5.1307e-05 | 0.00506467 | intron-variant | G2E3 | GRCh38.p7 | 14:30615548 | GTTGAAGGTATGTGG[A/C]TATTTTATTTTACTT | 55632 |
rs758053947 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30569719 | ACCTGCCCACGAAGT[C/T]AGGGTTAGGACCAGC | 55632 |
rs758135475 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30613529 | AGACTCATTTTGTAC[A/G]TTTTAGCCTAAGGAA | 55632 |
rs758159541 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30575088 | CTTACCCGCATCTGT[C/T]ATTTTTTGACTTTGT | 55632 |
rs758185812 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30585345 | TATATATGGTGTGAG[A/G]TAGGGGTTCACCTAT | 55632 |
rs758209735 | in-del | -/TATT | 4.50877e-05 | 0.00474782 | intron-variant | G2E3 | GRCh38.p7 | 14:30586697 | ATATATTTTTATATC[-/TATT]TACTTTTTCACTGTT | 55632 |
rs758234085 | snp | G/T | 1.69502e-05 | 0.00291115 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30593523 | ATTACATCTAATAAT[G/T]ATAGAGAGTCCTTAC | 55632 |
rs758291674 | snp | C/G/T | 3.62976e-05 | 0.00425999 | intron-variant | G2E3 | GRCh38.p7 | 14:30592479 | TTAAATATGAAAGTT[C/G/T]AGTGTTAAAGAATAG | 55632 |
rs758318881 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30601725 | CTAGTGGTTGAAACT[A/T]GAATAATAACAAAAT | 55632 |
rs758321945 | snp | A/G | 1.6659e-05 | 0.00288604 | missense, intron-variant | G2E3 | GRCh38.p7 | 14:30605690 | ATGTTATTGAAAATG[A/G]TAATTTTGGAAGTGA | 55632 |
rs758337341 | in-del | -/CAC | | | intron-variant | G2E3 | GRCh38.p7 | 14:30583663 | AATTTTAAGTATTCT[-/CAC]CACAAGTGGTAAATA | 55632 |
rs758348936 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30606923 | TGCCTTTGGGAAAGA[G/T]TATTTAGTGATATAG | 55632 |
rs758477611 | in-del | -/TC | | | downstream-variant-500B | G2E3 | GRCh38.p7 | 14:30620138 | ATTATTTTCAGTCTT[-/TC]TGATTCTAATAAAAC | 55632 |
rs758506984 | snp | C/G | 0.000190567 | 0.00975946 | intron-variant | G2E3 | GRCh38.p7 | 14:30560766 | TCAACAATGCTGATT[C/G]CTGCACTTCAGATCT | 55632 |
rs758551491 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30595534 | GTAGAAATAATATTA[C/G]TAACAAAAAAGACTA | 55632 |
rs758585928 | snp | A/C/G | 3.29501e-05 | 0.00405884 | missense, intron-variant, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30598538 | CTTCTGCAGCACTAT[A/C/G]AGCGTTGTGATGTTC | 55632 |
rs758630974 | snp | C/T | 1.67287e-05 | 0.00289207 | intron-variant | G2E3 | GRCh38.p7 | 14:30612193 | AAGTGGCTGTATTTT[C/T]TCCTTCATTACAGAT | 55632 |
rs758669545 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30566579 | TATTTGTGTGTTGAT[A/C]TTGCATCCTGTAACT | 55632 |
rs758679143 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30610342 | AGAATATGGCCGGGC[A/G]CAGTGGGTCACGCCT | 55632 |
rs758760304 | snp | A/G | 1.65715e-05 | 0.00287845 | intron-variant | G2E3 | GRCh38.p7 | 14:30592282 | TATTATAATACTCAG[A/G]TTTTTTATGTTGTGA | 55632 |
rs758792167 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30566022 | GTCGAAGAGACTGTT[A/T]TCTTCCCATTTAATG | 55632 |
rs758882939 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30587611 | GTCAGATTACAGCTG[A/G]AGACTTTACTAGGTT | 55632 |
rs758943225 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30589169 | TTTAGAAACTAATTA[A/G]GATATACAAACTGAT | 55632 |
rs758961930 | snp | C/T | 1.69235e-05 | 0.00290886 | intron-variant | G2E3 | GRCh38.p7 | 14:30589515 | TACTATTAAGTAATG[C/T]CATAAATATTGTCAA | 55632 |
rs758996668 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30600904 | TCTACCTTCTACAAT[G/T]GTGAGGATTAAACTT | 55632 |
rs759012058 | in-del | -/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30609102 | TTCTAAATCACACAG[-/T]TAAGCACTATTGAAG | 55632 |
rs759041432 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30560236 | AACTATAAATGGGAA[C/T]TTTAAATGTGTACAA | 55632 |
rs759068868 | snp | A/G | 2.26971e-05 | 0.00336868 | missense, intron-variant | G2E3 | GRCh38.p7 | 14:30605536 | AGAAGAAATGTATCA[A/G]CACTATTAATAGAGT | 55632 |
rs759106299 | snp | A/G | 1.66868e-05 | 0.00288845 | intron-variant | G2E3 | GRCh38.p7 | 14:30581136 | GTAACTGTATTTAAA[A/G]TAATTTTATTACAAT | 55632 |
rs759124341 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30572841 | GCTTCTAGTTTGAGG[A/G]ATGATAAAATTGAGG | 55632 |
rs759129445 | snp | A/G | 1.66629e-05 | 0.00288638 | synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616498 | AAACACTCTAAGACT[A/G]GAAAAGGAAGAAAGT | 55632 |
rs759202014 | snp | C/G | 1.64855e-05 | 0.00287097 | missense, intron-variant, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30598511 | GAATTAGAGGAAAAC[C/G]CTTATCAAGAGCTTC | 55632 |
rs759229900 | snp | A/C | 1.64746e-05 | 0.00287002 | intron-variant | G2E3 | GRCh38.p7 | 14:30598606 | ACCTGATAGGTATTT[A/C]TGAAAGTTCAGTTGT | 55632 |
rs759267560 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30610745 | GACAGTGGCTCAAAC[A/G]AGGCAGATGTTTACT | 55632 |
rs759287819 | snp | A/G | 3.47041e-05 | 0.00416544 | intron-variant | G2E3 | GRCh38.p7 | 14:30612163 | ATGTGCATGTCACTC[A/G]AAAGTAAATGAGTAA | 55632 |
rs759301102 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30582691 | TAGAATGTCCAATAT[A/G]AACAAATGGCAATTT | 55632 |
rs759396467 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30566484 | AATTTATTACTAAGT[A/G]ATTTTTATGCTATTG | 55632 |
rs759451799 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30565365 | TAATGTATTCTAGAT[A/G]CTAGACCCTTTTCAG | 55632 |
rs759486885 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30617165 | AGAATTAAGCTGGGC[A/G]CATGTGCTTGTAATC | 55632 |
rs759491656 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30577905 | TTAATTAAATTGTTT[A/G]TTTTCCAGGGAAGGG | 55632 |
rs759532611 | snp | C/G/T | 5.11499e-05 | 0.00505695 | missense, synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30608042 | AGATGATGTTTCAGA[C/G/T]TTTGATGTGGCACAG | 55632 |
rs759607762 | in-del | -/TTTG | | | intron-variant | G2E3 | GRCh38.p7 | 14:30615581 | AACGATCTCAGAATA[-/TTTG]TTTCAGCATATTTGT | 55632 |
rs759638975 | snp | A/G/T | 3.33702e-05 | 0.00408463 | splice-acceptor-variant | G2E3 | GRCh38.p7 | 14:30601998 | AAATTTAAATCTGTA[A/G/T]GAGAGTTCCAAAAAG | 55632 |
rs759664895 | snp | A/G | 1.86614e-05 | 0.00305456 | utr-variant-5-prime, missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30586808 | TCACTGTACATTACT[A/G]CTGTTTGGTGAGTAT | 55632 |
rs759670832 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30561701 | ATAGTGCGAGACTGC[C/T]CTTGTCCTTTTAATT | 55632 |
rs759730086 | snp | C/G | 1.64961e-05 | 0.00287189 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30615464 | GCAAAAATCCTTAGT[C/G]AGCTTTTTACAGTAC | 55632 |
rs759811219 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30569137 | TGTTCATTGTAAAAA[G/T]TCAAACAATGCCAAA | 55632 |
rs759903892 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30580406 | AAACAGGGTTTCACC[A/G]TGTTAGCCAGGCTGG | 55632 |
rs759939467 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30567953 | TTTGTGGTCTAACAT[A/G]GTATATCCATGGATA | 55632 |
rs759954139 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30591185 | GAATTCCTTGTTGTC[A/C]GTTCATTGGGAGAGT | 55632 |
rs759957467 | snp | A/T | 1.69882e-05 | 0.00291441 | intron-variant | G2E3 | GRCh38.p7 | 14:30593649 | TTACAGGTAAGATAC[A/T]TATTTTGTAAGCTTT | 55632 |
rs759977584 | in-del | -/TT | | | intron-variant | G2E3 | GRCh38.p7 | 14:30566426 | TTTCTTTCAGCACTG[-/TT]TTTTGTAGTTTTCAG | 55632 |
rs760015217 | in-del | -/A | 0.000300827 | 0.0122606 | intron-variant | G2E3 | GRCh38.p7 | 14:30597551 | ATTTAGCCTTATGAT[-/A]AAAAAAAGATATTTT | 55632 |
rs760054295 | snp | A/C | 2.39564e-05 | 0.00346087 | intron-variant | G2E3 | GRCh38.p7 | 14:30605824 | CAAGGTAATTATTTT[A/C]TTTATTGTTGTATAT | 55632 |
rs760081591 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30604760 | ATTTTCTTATATAGT[A/G]AGGAGAGATTACATT | 55632 |
rs760125501 | snp | A/G | 1.71161e-05 | 0.00292536 | missense, intron-variant | G2E3 | GRCh38.p7 | 14:30605603 | ATATCAACAAAGCCA[A/G]TATCTGGAATAGTGC | 55632 |
rs760178930 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30604943 | CTCTTGTTGCCCAGG[C/G]TGGAGTGCAATGGCG | 55632 |
rs760200981 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30563097 | TCTACAATCTCTCGT[C/T]TCCGCACACGGGGAG | 55632 |
rs760325772 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30561623 | GCCTTTTTATTTCCC[C/T]TTAAGATTTTACTCA | 55632 |
rs760350722 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30585143 | CCAGACAATAGTGTC[C/T]TTTGAGTCACAAAAG | 55632 |
rs760368944 | snp | A/T | 1.67942e-05 | 0.00289772 | intron-variant | G2E3 | GRCh38.p7 | 14:30581157 | TTATTACAATGAGTG[A/T]TTTAAATATGTTACT | 55632 |
rs760403608 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30598156 | TTGGGAGGCCGAGGC[A/G]GGCAGATCACCCAAG | 55632 |
rs760432783 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30583584 | TGGAATAAGTTCAAG[A/T]GATCTGTTGTACAAC | 55632 |
rs760451037 | snp | C/G | 1.64751e-05 | 0.00287007 | intron-variant | G2E3 | GRCh38.p7 | 14:30598617 | ATTTCTGAAAGTTCA[C/G]TTGTGCTTAGTGGTT | 55632 |
rs760492648 | snp | C/T | 1.64833e-05 | 0.00287078 | synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30601818 | TTCCAGTGGCACACA[C/T]TTAGCCTGCTCCTCA | 55632 |
rs760529380 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30584116 | ATCCATAAGTAAATT[A/G]AGTAATATTGTGACC | 55632 |
rs760634685 | snp | A/G | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30576864 | CAATTTCTCTTTCAA[A/G]TGCCTGATTCCAGCA | 55632 |
rs760653476 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30610835 | GTCACGTTCTGGCTT[C/G]TTGCCTGTTTGGTAA | 55632 |
rs760654369 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30596492 | TTACACATTCTCTCT[C/G]TTGCCGGGGAAACTT | 55632 |
rs760681642 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30588609 | AGAAAAGTATAGTGA[C/T]GTTACAAATGGCAAT | 55632 |
rs760697992 | snp | C/T | 1.65252e-05 | 0.00287443 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30612295 | GATGTCTCAGACTTA[C/T]AACGACATTAAGTGA | 55632 |
rs760721638 | snp | A/G | | | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558709 | GCCCTGACTGTGCCG[A/G]GATAGGACTGAGAGG | 55632 |
rs760732895 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30611995 | TCACGTAGTAAAGTG[A/G]CATTATACTCTGGAT | 55632 |
rs760733961 | snp | A/G | 1.65179e-05 | 0.00287379 | synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30589442 | AGTTTATGGTTTTCT[A/G]ATAGAAGATATCAGG | 55632 |
rs760753990 | in-del | -/TCTACTGTTA | 3.34591e-05 | 0.00409004 | intron-variant | G2E3 | GRCh38.p7 | 14:30597559 | TATGATAAAAAAAAG[-/TCTACTGTTA]ATATTTTAAATGTAG | 55632 |
rs760784198 | snp | C/T | 0.000188023 | 0.00969413 | intron-variant | G2E3 | GRCh38.p7 | 14:30590780 | GAGATATTAGTATCA[C/T]AATTCCTAAACTTCC | 55632 |
rs760810997 | snp | C/G | 1.65201e-05 | 0.00287398 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30602097 | CCTAAATTACCCAGA[C/G]AGTCACCTGGATCCC | 55632 |
rs760896888 | snp | A/T | 0.000102633 | 0.0071628 | intron-variant | G2E3 | GRCh38.p7 | 14:30616260 | TTCTTTTACTCTTTT[A/T]TTGGTAAATTTTTTC | 55632 |
rs760900820 | snp | A/G | 1.66252e-05 | 0.00288311 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30602013 | GGAGAGTTCCAAAAA[A/G]CCAAAAAACATGTAT | 55632 |
rs760956521 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30569362 | TAGGTATTATCATCT[C/G]CATTGGACACAAGGC | 55632 |
rs760986737 | snp | A/T | 1.6498e-05 | 0.00287206 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30615477 | GTGAGCTTTTTACAG[A/T]ACACACATTACCTGA | 55632 |
rs760995269 | in-del | -/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30579377 | ACAAAATATTGAAAG[-/C]TTAGAGTCAAAGCCA | 55632 |
rs761048477 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30570146 | AAATATGTCATCTCA[C/G]TGCCTTCTGGAACTC | 55632 |
rs761148016 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30614386 | CAGCATCTGGTGAGA[A/G]CTGTCTTGCTGTGTC | 55632 |
rs761154477 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30592976 | TTCTTTTAGTAGTTG[C/T]GTTTTTGACCTATTT | 55632 |
rs761210811 | snp | G/T | 1.65789e-05 | 0.0028791 | splice-donor-variant | G2E3 | GRCh38.p7 | 14:30597528 | CATATTCCTGAAAAG[G/T]GAGTAACATTTAGCC | 55632 |
rs761311065 | in-del | -/A | | | intron-variant | G2E3 | GRCh38.p7 | 14:30598231 | TCTACTAAAAAATAC[-/A]AAAAACCAGCCGGGC | 55632 |
rs761349047 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30581602 | AGCTACTCGCTAGGC[C/G]GAGGCAGGAGAATCG | 55632 |
rs761383259 | snp | C/T | 1.65359e-05 | 0.00287536 | synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30607994 | CTTGTTTAACTGCCT[C/T]GTTTATGGACCAGAA | 55632 |
rs761384800 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30563610 | ATGGGTGGTAGGGTG[C/G]GGTGGGGTAGGGGAG | 55632 |
rs761449206 | snp | C/T | 8.75496e-05 | 0.00661567 | intron-variant | G2E3 | GRCh38.p7 | 14:30593677 | TTTCTCTGATTGATA[C/T]AAAATTATGGCTTGC | 55632 |
rs761619152 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30561726 | TTAATTTTTATGTCT[C/G]CAGTGCACAGTGCAG | 55632 |
rs761633342 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30579574 | TGTGTCCTACATTTT[G/T]TGGTGTCTTAGATTT | 55632 |
rs761666975 | snp | G/T | 1.6631e-05 | 0.00288362 | intron-variant | G2E3 | GRCh38.p7 | 14:30589365 | GAGTTTATTTTCTAA[G/T]TGAGAATATATTCAT | 55632 |
rs761726664 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30599029 | CTGGAAGTTTAAGAT[C/G]AAGTTATTGACAGGT | 55632 |
rs761748144 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30566548 | ATTGTTCATTGTTAT[A/G]TAGAAATACAACTGA | 55632 |
rs761800400 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30608357 | GAAATACATGGATTT[C/G]CCTGCCTTGCTAGAG | 55632 |
rs761912712 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30610305 | ATCACGTAGTAAAAT[A/G]TATTATAATGCTAAA | 55632 |
rs761935106 | snp | A/C | 1.6902e-05 | 0.00290701 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30592410 | TTCCCATGTGGACTT[A/C]AGAGAGAATGTATTT | 55632 |
rs761942450 | snp | C/T | 3.69966e-05 | 0.00430081 | intron-variant | G2E3 | GRCh38.p7 | 14:30605477 | ACTTTAAAGTACTTA[C/T]CTCTATATTTAAATT | 55632 |
rs761944729 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30580451 | CCTCAGGTGATCCAC[C/T]TGCCTCAGCCTCCCA | 55632 |
rs761951331 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30600627 | ATTGGTCTCTCAATC[A/G]GTAGCTACAACTCTT | 55632 |
rs761990430 | in-del | -/T | 0.000531246 | 0.0162893 | intron-variant | G2E3 | GRCh38.p7 | 14:30605485 | GTACTTATCTCTATA[-/T]TTAAATTCATGTTTT | 55632 |
rs762116445 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30590365 | TGAGGTGGAGGAGTG[A/G]CTAGGAAGTTAGCAG | 55632 |
rs762146860 | snp | C/T | | | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30557828 | CAGTACATCAGTTAA[C/T]AGCTTTACACACCCC | 55632 |
rs762167810 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30602307 | AGCATTTTAAAGAAA[A/G]TGAAATGGGATAGAA | 55632 |
rs762169893 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30588981 | TAGAGTTAGCCTGAA[A/C]TGTCACTGAATTAAT | 55632 |
rs762206212 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30582437 | CATACTGGGTAGAGG[G/T]AGACAAGGGGAGAGA | 55632 |
rs762208409 | snp | C/T | 3.30989e-05 | 0.00406797 | synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30615503 | CCTGATGTGAAAGCT[C/T]TGGGGTTTTGGAACA | 55632 |
rs762276811 | snp | A/G | 1.67452e-05 | 0.0028935 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616289 | TCAGATGGTAAATCT[A/G]CAACAACAATGGAAG | 55632 |
rs762283149 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30570277 | TTTGTCAGTTTGACT[A/G]TACTGTGTCTCAATG | 55632 |
rs762402087 | in-del | -/GG | | | intron-variant | G2E3 | GRCh38.p7 | 14:30611293 | ATTATTACTCCGACA[-/GG]GTGTAAAGATAGTAT | 55632 |
rs762475074 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30571500 | ATGATTCAGTTTCCT[A/G]AGAAATCTTTGCCAA | 55632 |
rs762481676 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616555 | TTCCTTGAACAAAGA[A/G]AAGCTTCTTTAAAAG | 55632 |
rs762500417 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30581650 | GAAGTTGCAGTGAGC[A/G]GAGATCGCACCACTA | 55632 |
rs762505721 | in-del | -/CT | | | intron-variant | G2E3 | GRCh38.p7 | 14:30601115 | TTACCTCTCTTGCCA[-/CT]CACACACACGGGGAG | 55632 |
rs762510067 | snp | A/G | 1.64931e-05 | 0.00287163 | missense, intron-variant, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30598505 | TCCTGGGAATTAGAG[A/G]AAAACGCTTATCAAG | 55632 |
rs762529983 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30582660 | GGGGATGGAGTTAAG[A/G]TGGAGCTTACTGGTG | 55632 |
rs762599227 | snp | G/T | 1.77628e-05 | 0.00298011 | intron-variant | G2E3 | GRCh38.p7 | 14:30612136 | AGTATAAATTAACAA[G/T]TATCATTTGAAATGT | 55632 |
rs762601169 | snp | A/T | 3.34616e-05 | 0.00409019 | intron-variant | G2E3 | GRCh38.p7 | 14:30597551 | ATTTAGCCTTATGAT[A/T]AAAAAAAGATATTTT | 55632 |
rs762682478 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30595098 | TGCTGAGATAGCACC[A/G]CTGCACTCCTGTCTG | 55632 |
rs762735432 | snp | C/T | | | synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30593582 | GCCTATTCCAAGTTA[C/T]AACATATTACGAAGT | 55632 |
rs762742279 | snp | A/G | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30576734 | AGGAATTTAGAGTAC[A/G]TCGAATAATGCAATG | 55632 |
rs762747953 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30617674 | GTCACCACTCAGAGA[C/T]AAGTACCGTATTTCT | 55632 |
rs762812703 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30563424 | CCCAACAAAACTGGT[A/G]CAGGTATTTATATCA | 55632 |
rs762863030 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30588076 | TCAAAGGTTAAATAG[A/C]GTAGTAGACTGGCCT | 55632 |
rs762964682 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30612018 | CTCTGGATTTCTTGA[A/G]GGCAGAAATAGACAA | 55632 |
rs762985458 | snp | A/C | 1.6554e-05 | 0.00287693 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30612323 | TGATAAATATATGTT[A/C]GTAAAAGACATACTT | 55632 |
rs763015379 | snp | A/T | 1.65776e-05 | 0.00287898 | intron-variant | G2E3 | GRCh38.p7 | 14:30589375 | TCTAATTGAGAATAT[A/T]TTCATAGTTGATGTC | 55632 |
rs763043561 | snp | C/T | 4.08322e-05 | 0.00451823 | intron-variant | G2E3 | GRCh38.p7 | 14:30615306 | TAATATAATACCAAA[C/T]ACACATGTATGAATG | 55632 |
rs763118158 | snp | C/T | 5.1553e-05 | 0.0050768 | intron-variant | G2E3 | GRCh38.p7 | 14:30593428 | GTGTTTTCCAAGTTT[C/T]GCTTTGCAGTTCATG | 55632 |
rs763206113 | snp | A/G | 1.74949e-05 | 0.00295756 | missense, intron-variant | G2E3 | GRCh38.p7 | 14:30605593 | AAAAGATTGTATATC[A/G]ACAAAGCCAATATCT | 55632 |
rs763240563 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30590418 | TAGGCTCAAAGGTCC[A/G]AATTTTTCAAAGTGT | 55632 |
rs763277626 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30573002 | TCATATTGATGTTTT[A/G]TGTACTTTTTTTTTG | 55632 |
rs763315242 | in-del | -/AC | | | intron-variant | G2E3 | GRCh38.p7 | 14:30572268 | TGATCATATGTGAAA[-/AC]ACAGTTTTACTTCAT | 55632 |
rs763339027 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30591025 | TGTTGGCACTCAGAA[A/G]GTTTCCTATTTTGAA | 55632 |
rs763347729 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30572700 | TATTTCTAAGATAAA[C/T]CCAGTTAAGATATAT | 55632 |
rs763369950 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30602881 | CCTCCCAAAATGTTG[C/G]GATTACAGGTGTGCG | 55632 |
rs763370898 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30578306 | GCTTAGAGAAAAGTT[G/T]TAAGAATGGCATAAG | 55632 |
rs763386416 | snp | A/G | 0.0001184 | 0.00769325 | intron-variant | G2E3 | GRCh38.p7 | 14:30602145 | AGGTATGTATTTTGA[A/G]TTGGAGAAATACATA | 55632 |
rs763445420 | snp | A/G | 2.50009e-05 | 0.00353551 | synonymous-codon, intron-variant | G2E3 | GRCh38.p7 | 14:30605517 | TAGGCAAGGCAGCAA[A/G]TTTAGAAGAAATGTA | 55632 |
rs763515762 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30570065 | TTCACTTTTGAAACA[G/T]AGTTTTGCTGCAGAT | 55632 |
rs763541897 | snp | A/G | 2.36611e-05 | 0.00343947 | intron-variant | G2E3 | GRCh38.p7 | 14:30593455 | CATGAGATTTTTTTA[A/G]AATAATTTACATTTT | 55632 |
rs763569314 | snp | A/G | 1.66313e-05 | 0.00288364 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616478 | AATATGGACTTCACC[A/G]TAAGAAACACTCTAA | 55632 |
rs763630844 | snp | A/C | 1.66804e-05 | 0.00288789 | missense, intron-variant | G2E3 | GRCh38.p7 | 14:30605651 | ATCGAAACTTTAATC[A/C]TTCATATGCAATTGA | 55632 |
rs763654656 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30587812 | AGAGAAATCAAGATG[G/T]AACCATATGACCTAG | 55632 |
rs763708068 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30561519 | TCATAATATTACACC[A/G]GTCTCTTCCAACCTG | 55632 |
rs763733235 | snp | G/T | 1.73039e-05 | 0.00294137 | utr-variant-5-prime, missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30586782 | AAAGAAAACTAAGGA[G/T]AAATGGAATCTCACT | 55632 |
rs763761586 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30573137 | TGTGCCTGGCTTTTA[A/T]GTACATTTTTAAGAT | 55632 |
rs763769176 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30561647 | TTACTCAAATGGGTT[G/T]AAAGACTTCTCCAGG | 55632 |
rs763820172 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30604973 | GTGATCTTGGCTCAA[C/T]GCAACCTCTGCTTCC | 55632 |
rs763820622 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30585582 | GTTTTTAATCTTCTC[A/C]CCCTTTTTTTTTTTG | 55632 |
rs763841599 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30618498 | TGATTAAGTCACACA[C/T]ACATACTTTGTTGGG | 55632 |
rs763863059 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30574586 | CTCCCACCCTCCTGC[A/G]TCAGGTAGACCCCAG | 55632 |
rs763877040 | snp | A/G | | | synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30608021 | AGAAAATACCCAGCC[A/G]ATTTTAGATGATGTT | 55632 |
rs763894374 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30560460 | TCTTCCTGCTATTGA[A/C]CTTTTAAGTGTTAGC | 55632 |
rs763943192 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | G2E3 | GRCh38.p7 | 14:30619534 | CAATACAAAGTTTCA[C/T]GCTTCAAGTAATGCA | 55632 |
rs763959538 | snp | A/G | 1.67804e-05 | 0.00289653 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616530 | CTCATTACATTGGAC[A/G]TTAAAATGTTTCCTT | 55632 |
rs764026229 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30596609 | TTTACTAACCCTCTG[A/C]CATAATTATCAGTAT | 55632 |
rs764088500 | snp | C/G | 1.64751e-05 | 0.00287007 | intron-variant | G2E3 | GRCh38.p7 | 14:30598620 | TCTGAAAGTTCAGTT[C/G]TGCTTAGTGGTTCCT | 55632 |
rs764101354 | snp | C/T | 0.000189054 | 0.00972066 | intron-variant | G2E3 | GRCh38.p7 | 14:30590793 | CATAATTCCTAAACT[C/T]CCTGGTGATAGTGAG | 55632 |
rs764109884 | in-del | -/CTT | 3.29554e-05 | 0.00405914 | cds-indel, intron-variant, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30598523 | AACGCTTATCAAGAG[-/CTT]CTGCAGCACTATGAG | 55632 |
rs764119200 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30563519 | ACAAGACTATTGGAA[A/G]CCAAGCTGGAAAGGT | 55632 |
rs764180835 | snp | A/G | 1.65318e-05 | 0.002875 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30612307 | TTATAACGACATTAA[A/G]TGATAAATATATGTT | 55632 |
rs764182505 | snp | C/T | 1.64754e-05 | 0.00287009 | synonymous-codon, intron-variant, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30598534 | AGAGCTTCTGCAGCA[C/T]TATGAGCGTTGTGAT | 55632 |
rs764183811 | snp | C/T | 1.64808e-05 | 0.00287057 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30601786 | AAATGGGAAATAAAG[C/T]GCTGTCAGTGTTGTG | 55632 |
rs764205886 | snp | C/T | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30576904 | TATATTCAATGTCAC[C/T]TTTTTCAGTAAGATT | 55632 |
rs764224421 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30587337 | AATTAGTCTCCCTTT[G/T]TTCCCCCTCCCCTCC | 55632 |
rs764227915 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30608831 | GATTAAAAGCATAGG[A/C]CTTAGCCAGGCGTGG | 55632 |
rs764266106 | snp | C/T | 1.65307e-05 | 0.0028749 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30602103 | TTACCCAGACAGTCA[C/T]CTGGATCCCAGAGTA | 55632 |
rs764269393 | snp | A/C | | | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30557593 | TAGGTATCCATCCCA[A/C]AACTTTGTATACCAT | 55632 |
rs764302602 | in-del | -/T | 0.00020319 | 0.0100774 | intron-variant | G2E3 | GRCh38.p7 | 14:30560856 | GGTTAGAAAATACTG[-/T]TGAGTTTTCAAAACA | 55632 |
rs764346943 | snp | A/G | 1.67318e-05 | 0.00289234 | intron-variant | G2E3 | GRCh38.p7 | 14:30589493 | TAAACTGGTAAGTAA[A/G]TTATTTTACTATTAA | 55632 |
rs764355915 | snp | A/G | 1.66178e-05 | 0.00288247 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30602016 | GAGTTCCAAAAAGCC[A/G]AAAAACATGTATTAC | 55632 |
rs764413398 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30600536 | ATAGAATTTTAAGAA[A/G]CAATACATTCATAAT | 55632 |
rs764445890 | snp | C/T | 1.64977e-05 | 0.00287203 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30615479 | GAGCTTTTTACAGTA[C/T]ACACATTACCTGATG | 55632 |
rs764533835 | snp | C/T | 1.7849e-05 | 0.00298734 | synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30615349 | TTTTCTTCTCTTAAG[C/T]TTTAAGCAGGGTCTG | 55632 |
rs764608086 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30569364 | GGTATTATCATCTCC[A/G]TTGGACACAAGGCAG | 55632 |
rs764647673 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30614790 | TCAGTTGTTACTTGC[A/G]TTTCTTTTGTTAATC | 55632 |
rs764716153 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30612689 | ATGGTGAAACCCCGT[A/C]TGTACTAAAATACAA | 55632 |
rs764751462 | snp | A/T | 0.00010308 | 0.00717838 | intron-variant | G2E3 | GRCh38.p7 | 14:30593427 | AGTGTTTTCCAAGTT[A/T]TGCTTTGCAGTTCAT | 55632 |
rs764789703 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30613278 | CAGTATTATTTTAAA[A/G]CCAATACCAGATATC | 55632 |
rs764829501 | snp | C/T | 1.66571e-05 | 0.00288587 | intron-variant | G2E3 | GRCh38.p7 | 14:30597542 | GTGAGTAACATTTAG[C/T]CTTATGATAAAAAAA | 55632 |
rs764930291 | snp | A/G | 7.0205e-05 | 0.00592432 | intron-variant | G2E3 | GRCh38.p7 | 14:30605856 | CCAAATATCACATGT[A/G]TAGAAAAAGAGATAG | 55632 |
rs764986058 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30608592 | AGGACTTAATGCGTC[C/T]GCCTAAAAATAGTTC | 55632 |
rs764987566 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30563314 | TTTCTTTAAAAACCT[A/G]CCCAACAATGTAGGG | 55632 |
rs765025682 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30574665 | CCACTTACAAGTGAG[A/G]ACATGCGGTATTTGG | 55632 |
rs765111923 | snp | C/T | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30575893 | CAAATGGAAAAACAT[C/T]CCATGCTCATGTATA | 55632 |
rs765212132 | snp | A/G | | | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558904 | CATTTTGGAAAAAAG[A/G]GGATCCCCTCAAGAG | 55632 |
rs765257957 | snp | C/T | 1.75486e-05 | 0.0029621 | utr-variant-5-prime, missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30586792 | AAGGAGAAATGGAAT[C/T]TCACTGTACATTACT | 55632 |
rs765288644 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B | G2E3 | GRCh38.p7 | 14:30619848 | CTAAAGGTAAACTGC[C/G]TATTTAAACTAAGTA | 55632 |
rs765289050 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30610856 | TGTTTGGTAAATAGT[C/T]ACATTGGAATGCAGC | 55632 |
rs765339841 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30610316 | AAATGTATTATAATG[C/G]TAAATAAAACAGAAT | 55632 |
rs765343180 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30595426 | TATTTGTTAATAATT[A/T]AGCAAAGAAAGGTTC | 55632 |
rs765391061 | in-del | -/T | | | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30557902 | ACCTTTCAAACTGTA[-/T]TTTTTTTTTTTTTTT | 55632 |
rs765395961 | in-del | -/TAAA | | | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30618629 | AGTGATAAGATGGTG[-/TAAA]TAAATAATTTAGGAT | 55632 |
rs765408925 | snp | C/G | 1.69772e-05 | 0.00291347 | intron-variant | G2E3 | GRCh38.p7 | 14:30612180 | AAGTAAATGAGTAAA[C/G]TGGCTGTATTTTCTC | 55632 |
rs765444535 | snp | A/C | 1.69089e-05 | 0.0029076 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30592411 | TCCCATGTGGACTTC[A/C]GAGAGAATGTATTTT | 55632 |
rs765501357 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30578281 | TAATTTGATACTGCT[A/G]TAATTTCAAGCTTAG | 55632 |
rs765550871 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30596068 | TGCTCAAATATCCTT[C/T]AGGTTCAGAGATTTC | 55632 |
rs765551019 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30567499 | GTCTGTAGCAGTGTC[C/T]CACTTTCATTTCTTC | 55632 |
rs765612261 | snp | C/G | | | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558928 | TCAAGAGCAAATAGG[C/G]GGAAACAATGACCCC | 55632 |
rs765638476 | snp | A/G | 1.67382e-05 | 0.00289289 | synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616291 | AGATGGTAAATCTAC[A/G]ACAACAATGGAAGAC | 55632 |
rs765663700 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30571319 | TTTATTGTGATGTCT[A/C]TTTGAGTTGTAAGCA | 55632 |
rs765665571 | snp | C/T | | | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30557998 | GCTCACTGCAAGCTC[C/T]GTCTCCCGGGTTCAC | 55632 |
rs765673376 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30599717 | AATTTTTATGTAGAT[A/T]ACATATTGAACAAAA | 55632 |
rs765678474 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30589034 | CACCACTCCTTTTTG[A/T]TAAGCTTAATTGTAG | 55632 |
rs765738124 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30600781 | AAGCTAGATAAACTG[A/G]AATGGAATCCTCACT | 55632 |
rs765759146 | in-del | -/AT | | | intron-variant | G2E3 | GRCh38.p7 | 14:30608651 | TACTAAACATGTCAC[-/AT]GTGCAAACACTCATT | 55632 |
rs765789146 | snp | A/G | | | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616329 | TTTTTGCAACTGGTT[A/G]CAGTTCCATTCCTCC | 55632 |
rs765791844 | in-del | -/GG | | | intron-variant | G2E3 | GRCh38.p7 | 14:30573423 | ATGTGTGTGTGTGTG[-/GG]TGTGTGTGCGTGTGT | 55632 |
rs765836158 | snp | G/T | 1.67866e-05 | 0.00289707 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30615530 | AACAGTTACTTACAG[G/T]CTGTTGAAGGTATGT | 55632 |
rs765862954 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30617888 | TGATGTCCTTAATCT[A/G]TTAACATATTTAAAT | 55632 |
rs765992747 | snp | A/T | 1.66668e-05 | 0.00288672 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616313 | ATGGAAGACATTCTT[A/T]TTTTTGCAACTGGTT | 55632 |
rs766015758 | snp | A/G | 1.64904e-05 | 0.00287139 | synonymous-codon, intron-variant, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30598507 | CTGGGAATTAGAGGA[A/G]AACGCTTATCAAGAG | 55632 |
rs766123213 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30581664 | CAGAGATCGCACCAC[C/T]ACACTTCAGCCTAAG | 55632 |
rs766132685 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30595156 | AAAAAATGCAGGATG[A/C]AGCCTGTTTTGTTGG | 55632 |
rs766135291 | in-del | -/A/AA | 0.0555076 | 0.158196 | frameshift-variant, intron-variant | G2E3 | GRCh38.p7 | 14:30605565 | TTAGGATTCCAAATT[-/A/AA]AAAAAAAAAACTAAA | 55632 |
rs766190364 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30608705 | CATTGCCAACATGTT[A/T]CTGCTTTAAAAACTG | 55632 |
rs766192105 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30572539 | AATTCCCGTCTGTTT[C/T]TGGTTTGTCCTACAG | 55632 |
rs766193968 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30565191 | TGGACATGAAGTGGT[A/G]TCTCATTGTGGCTTT | 55632 |
rs766208597 | snp | A/G | 0.000117387 | 0.00766027 | intron-variant | G2E3 | GRCh38.p7 | 14:30607843 | AATGATGGTTATCTT[A/G]TAATAATAGAAGTGT | 55632 |
rs766228260 | snp | A/C/G | 0.000101875 | 0.00713641 | synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30608039 | TTTAGATGATGTTTC[A/C/G]GACTTTGATGTGGCA | 55632 |
rs766249003 | snp | A/G | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30576758 | TGCAATGCATAGACT[A/G]AGTTGAACCTTTCTG | 55632 |
rs766326201 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30581809 | CTTTGCTTTTAATTG[C/T]TGTTTTCTTCATTTA | 55632 |
rs766371738 | snp | G/T | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30575939 | ATTAAAATGGCTATT[G/T]TGCCCAAAACAATTT | 55632 |
rs766404898 | snp | C/G | 2.03772e-05 | 0.00319189 | intron-variant | G2E3 | GRCh38.p7 | 14:30615308 | ATATAATACCAAACA[C/G]ACATGTATGAATGTT | 55632 |
rs766427129 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30584253 | TCATATGGGCATACC[A/G]TATTTTGTTTATCCA | 55632 |
rs766506513 | snp | A/G | 5.16142e-05 | 0.00507981 | intron-variant | G2E3 | GRCh38.p7 | 14:30586694 | TAAATATATTTTTAT[A/G]TCTATTTACTTTTTC | 55632 |
rs766510980 | snp | A/C/T | 0.000148382 | 0.00861225 | synonymous-codon, missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30601837 | GCCTGCTCCTCATTA[A/C/T]GGTCATGGGAGCAAA | 55632 |
rs766524152 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30611098 | TTTGCATCCACATGG[C/T]TGAAGCTTGCTCTTA | 55632 |
rs766552274 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30596759 | CTGTCATGTTTTTTG[C/G]TACATAATACCAAAT | 55632 |
rs766587754 | snp | A/G | 1.65452e-05 | 0.00287616 | synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30612221 | GATAAATACTGCAAC[A/G]ACTGTAGCTGACTTA | 55632 |
rs766602500 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30605116 | GGTCACACTGGTCTC[A/G]AACTCATGACCTCAG | 55632 |
rs766604409 | snp | G/T | 1.6554e-05 | 0.00287693 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30612324 | GATAAATATATGTTA[G/T]TAAAAGACATACTTG | 55632 |
rs766736119 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30592903 | ATTTGCTTCCTGAGT[A/T]CAACTTTAAACATCA | 55632 |
rs766820462 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30578393 | GTTATTCTTTGTCTC[A/G]TCCTAGCCCAGTCAG | 55632 |
rs766860022 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30590541 | GTCAAGTCTGGAAAT[G/T]AAGGAGGATGGAAAA | 55632 |
rs766882085 | snp | G/T | 1.65567e-05 | 0.00287716 | intron-variant | G2E3 | GRCh38.p7 | 14:30592291 | ACTCAGATTTTTTAT[G/T]TTGTGACCCCTATTT | 55632 |
rs766965461 | snp | C/T | 2.47179e-05 | 0.00351544 | missense, intron-variant | G2E3 | GRCh38.p7 | 14:30605519 | GGCAAGGCAGCAAAT[C/T]TAGAAGAAATGTATC | 55632 |
rs766972192 | snp | A/C/T | 3.42098e-05 | 0.00413569 | intron-variant | G2E3 | GRCh38.p7 | 14:30602158 | GAATTGGAGAAATAC[A/C/T]TAAAAATCTATTTGG | 55632 |
rs766974539 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | G2E3 | GRCh38.p7 | 14:30619423 | GAACAAAATCATTAC[A/G]TTATAAACATGTAAT | 55632 |
rs767051349 | snp | A/T | 1.66352e-05 | 0.00288398 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616483 | GGACTTCACCATAAG[A/T]AACACTCTAAGACTA | 55632 |
rs767058375 | snp | A/G | 1.66916e-05 | 0.00288886 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616511 | CTAGAAAAGGAAGAA[A/G]GTTCTCATTACATTG | 55632 |
rs767078188 | snp | C/T | 1.74946e-05 | 0.00295753 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30592444 | AGTTTACTGGCAATT[C/T]TGCGTGAGTTATTTA | 55632 |
rs767143976 | snp | A/G | | | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30559098 | GCCAGCGCCTCCGCG[A/G]GTCCCACCCCTCGAG | 55632 |
rs767155018 | snp | A/G | 1.67281e-05 | 0.00289202 | intron-variant | G2E3 | GRCh38.p7 | 14:30581147 | TAAAATAATTTTATT[A/G]CAATGAGTGTTTTAA | 55632 |
rs767169738 | snp | A/C | 2.24732e-05 | 0.00335203 | synonymous-codon, intron-variant | G2E3 | GRCh38.p7 | 14:30605538 | AAGAAATGTATCAAC[A/C]CTATTAATAGAGTTA | 55632 |
rs767223386 | in-del | -/CT | | | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30557844 | AGCTTTACACACCCC[-/CT]GTGTCAGATTACCTG | 55632 |
rs767224902 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30572894 | ATAGAACATGAAGGA[A/G]AGTCTAAACTTCATA | 55632 |
rs767317800 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30596310 | TCACTGCTTTAATTT[C/T]AGACACTCTTTTTGG | 55632 |
rs767318965 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30563614 | GTGGTAGGGTGGGGT[A/G]GGGTAGGGGAGGATG | 55632 |
rs767365362 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30610186 | AATACTATGTATTCT[A/G]TACTGTTTTGTTACT | 55632 |
rs767366194 | in-del | -/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30603851 | CTTGTCTCTAAAAAG[-/T]TTCAAGTTTAAAACC | 55632 |
rs767376750 | snp | C/G | 1.64806e-05 | 0.00287054 | missense, intron-variant, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30598517 | GAGGAAAACGCTTAT[C/G]AAGAGCTTCTGCAGC | 55632 |
rs767396735 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30582754 | GAAGGGAAGGAAGAG[G/T]AGCTGAAATCTTTTA | 55632 |
rs767423001 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30608438 | ACTTTGATGGAGGCC[A/G]ATGGGTCTGAAGAGA | 55632 |
rs767430353 | snp | C/G | 1.65195e-05 | 0.00287393 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30589396 | AGTTGATGTCAAGTG[C/G]AATTTGGCAGAGAGG | 55632 |
rs767466709 | snp | A/C | 1.73126e-05 | 0.00294211 | intron-variant | G2E3 | GRCh38.p7 | 14:30612165 | GTGCATGTCACTCAA[A/C]AGTAAATGAGTAAAG | 55632 |
rs767503542 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30594212 | AATTTAATAATTCTT[G/T]GATTCTGAAAATACT | 55632 |
rs767560416 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616836 | GGTATGGTAGCATGG[-/T]TAATAAAAGTAAAAA | 55632 |
rs767612141 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30587248 | TGGCTAAAGGTGATA[A/C]ATATTTTTGGAAAAG | 55632 |
rs767708798 | in-del | -/AA | | | intron-variant | G2E3 | GRCh38.p7 | 14:30567623 | ATTGATTCTCAATTT[-/AA]AAATTTTTTTATTAC | 55632 |
rs767736863 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30599185 | CCAGTCATTTGGTTT[A/C]GGGCCCACCTATCTG | 55632 |
rs767739435 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30580423 | GTTAGCCAGGCTGGT[C/G]TCGAACTCCTGACCT | 55632 |
rs767750831 | snp | C/T | 1.64898e-05 | 0.00287135 | synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30601854 | GTCATGGGAGCAAAA[C/T]TGGGAGTGTTTGGAA | 55632 |
rs767786629 | snp | C/T | 1.98517e-05 | 0.00315047 | intron-variant | G2E3 | GRCh38.p7 | 14:30615322 | ACACATGTATGAATG[C/T]TGGCTCATTATTTTT | 55632 |
rs767873102 | snp | A/G | 1.67091e-05 | 0.00289038 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30612351 | CTTGGCTACCATGTA[A/G]TTCAGAGAGTCCACA | 55632 |
rs767894482 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30568011 | TTTCATTCTGTTGTA[A/G]GGTGGAGTGTTCTGT | 55632 |
rs767925431 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30588637 | AATAGAATGCTAGAG[C/T]GGAAAGAGACTTAGA | 55632 |
rs767991087 | snp | C/T | 1.65285e-05 | 0.00287471 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30607953 | TTAGTTCACGGTGGT[C/T]CTTCACCTGGTTTCT | 55632 |
rs768016189 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30591205 | ATTGGGAGAGTTTCG[A/G]GTTGGCAGGTATTCT | 55632 |
rs768037085 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30611507 | GAAAGTGTCTTGCAC[A/G]TAAATGGCCAAGTAT | 55632 |
rs768089134 | snp | G/T | 0.00018859 | 0.00970874 | intron-variant | G2E3 | GRCh38.p7 | 14:30590606 | AGCACATAAGAAACA[G/T]TTATTCTTTTAGTTG | 55632 |
rs768106656 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30593446 | TTTGCAGTTCATGAG[A/G]TTTTTTTAAAATAAT | 55632 |
rs768124129 | snp | A/G | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30575829 | AGGTGAAAGATCTCT[A/G]CAATGAGAATTACAA | 55632 |
rs768192855 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30608385 | GAGACAACGTGAGGC[A/G]GATTCCCTATTGCAA | 55632 |
rs768194670 | snp | A/G | 1.67237e-05 | 0.00289164 | missense, intron-variant | G2E3 | GRCh38.p7 | 14:30605636 | TAGATGCATTCAGAA[A/G]TCGAAACTTTAATCC | 55632 |
rs768254636 | snp | C/T | 3.42706e-05 | 0.00413934 | intron-variant | G2E3 | GRCh38.p7 | 14:30586866 | GTGTTCTAAAGAAGA[C/T]AGTAAGATTCTGACA | 55632 |
rs768289165 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30587684 | GGCCTCAATTTCTCC[G/T]AGCTAGCGTCAGGAA | 55632 |
rs768292485 | in-del | -/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30590698 | AAAACAGAGGTTCTA[-/G]GGCACAAGGAAGAAC | 55632 |
rs768338052 | snp | C/G/T | 3.33196e-05 | 0.00408153 | intron-variant | G2E3 | GRCh38.p7 | 14:30589361 | CTTAGAGTTTATTTT[C/G/T]TAATTGAGAATATAT | 55632 |
rs768348802 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30569831 | TCAGCAAGAGCAACT[C/T]CCAGAAGAAATTCCT | 55632 |
rs768412758 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30598985 | ACTGGGTGGCTTAAA[A/G]TAAATTTATTTTCTC | 55632 |
rs768503100 | snp | A/G | 3.38061e-05 | 0.00411119 | intron-variant | G2E3 | GRCh38.p7 | 14:30601960 | TAAAAGTTTTTACCT[A/G]TATCTCTATTATGCT | 55632 |
rs768522737 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30567668 | TAAATTATTTCCTTC[C/G]TTCTGCTAGCTTTGG | 55632 |
rs768590633 | snp | A/G | 3.2969e-05 | 0.00405998 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30601822 | AGTGGCACACATTTA[A/G]CCTGCTCCTCATTAC | 55632 |
rs768630949 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30559558 | TTTATACGCATCCTC[C/T]GTGGCTTTTTTTAAA | 55632 |
rs768652561 | snp | A/C | 1.67144e-05 | 0.00289084 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30592398 | CGAAGTTATCATTTC[A/C]CATGTGGACTTCAGA | 55632 |
rs768652581 | snp | G/T | 7.16089e-05 | 0.00598325 | missense, intron-variant | G2E3 | GRCh38.p7 | 14:30605585 | AAAAAACTAAAAGAT[G/T]GTATATCAACAAAGC | 55632 |
rs768680569 | snp | A/G | 3.61219e-05 | 0.00424967 | intron-variant | G2E3 | GRCh38.p7 | 14:30612431 | TACATGTTTAAAGTG[A/G]TTAATTATCTTGTAA | 55632 |
rs768712394 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30588555 | AAAAAAGTACTGACC[C/T]CAGACTTAACCCTTT | 55632 |
rs768729025 | snp | C/G | 1.66468e-05 | 0.00288498 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616425 | GTAATAACTGTTTAG[C/G]AATTCCCATCACCAA | 55632 |
rs768740517 | snp | C/G | 3.83281e-05 | 0.00437751 | intron-variant | G2E3 | GRCh38.p7 | 14:30605470 | ATAAAGTACTTTAAA[C/G]TACTTATCTCTATAT | 55632 |
rs768764250 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30580209 | TTGTTTTTGTTTTTT[G/T]TTGTTGTTGTTTTTG | 55632 |
rs768810379 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30559710 | GGGCGGGTTTAGAAT[A/G]AAAAGATGCTCTACG | 55632 |
rs768912218 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30571086 | TTTTCTAGAAATTTT[A/G]TAGTTTTACATTTTG | 55632 |
rs768923421 | snp | C/T | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30576144 | CTCCAGTAACCAAAA[C/T]AGCATAGTACTGGTA | 55632 |
rs768926768 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30617595 | CATTGCTCTTGAATG[A/G]TATCTGTTATATAAG | 55632 |
rs768934137 | in-del | -/TGTG | | | intron-variant | G2E3 | GRCh38.p7 | 14:30563698 | ACTTTGTTACTTTTG[-/TGTG]TGTGTGTGTGTGTGT | 55632 |
rs768975951 | snp | A/G | 1.70148e-05 | 0.00291669 | intron-variant | G2E3 | GRCh38.p7 | 14:30616264 | TTTACTCTTTTATTG[A/G]TAAATTTTTTCAGAT | 55632 |
rs769020370 | in-del | -/A | | | intron-variant | G2E3 | GRCh38.p7 | 14:30607340 | TCATAAAGTATACTT[-/A]ACGCAAACCTAGTTG | 55632 |
rs769035622 | snp | A/G | 1.65149e-05 | 0.00287353 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30597475 | CAATATGCAATAATA[A/G]TGACATCTTTCAGAA | 55632 |
rs769117069 | snp | A/G | 1.68091e-05 | 0.00289901 | intron-variant | G2E3 | GRCh38.p7 | 14:30598452 | TAACATTATTTATAG[A/G]TCAAAGCATATTTTA | 55632 |
rs769121665 | snp | C/T | 1.65916e-05 | 0.00288019 | intron-variant | G2E3 | GRCh38.p7 | 14:30598480 | TTATATCTTCTTTTA[C/T]AGAGATGCTTCCTGG | 55632 |
rs769129912 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30616169 | CAAATGTGGGAGTCT[C/G]TGCCTTTCAGTATTC | 55632 |
rs769226899 | snp | A/G | 1.65247e-05 | 0.00287438 | synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30612239 | TGTAGCTGACTTAAA[A/G]TCAATAATAAATGAA | 55632 |
rs769264718 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30564657 | GCCATTTTAAAGTAG[A/G]CATTTCAGTGACAGT | 55632 |
rs769320735 | snp | A/G | 1.78344e-05 | 0.00298611 | intron-variant | G2E3 | GRCh38.p7 | 14:30612122 | TACTAAGAAATTTGA[A/G]TATAAATTAACAAGT | 55632 |
rs769326379 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30564483 | GACTACAGGCATTTG[C/T]CACCAAGACTGGCTA | 55632 |
rs769363370 | in-del | -/AT | 9.94711e-05 | 0.00705164 | intron-variant | G2E3 | GRCh38.p7 | 14:30592273 | CTTGATCATATTATA[-/AT]ATACTCAGATTTTTT | 55632 |
rs769370075 | snp | A/G | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30577564 | TAACATGGCTTATTC[A/G]CATAACAGAAGGTAG | 55632 |
rs769391142 | snp | A/G | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30576588 | GTAAACAGACAACCT[A/G]CAGAATAGGAGAAAA | 55632 |
rs769399981 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30610593 | GGGCAACAGAGTGAG[A/G]CTCCATCCCAAATAA | 55632 |
rs769429052 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30572675 | ACTTTTCAGATGATA[A/T]CTAATCTTATATTTC | 55632 |
rs769526214 | snp | G/T | 4.95569e-05 | 0.00497755 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30602062 | TGGGGATTACAGATT[G/T]TTTGTTGGAAGAGTC | 55632 |
rs769526479 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30609539 | CTTAGCATTTTTCAG[G/T]GTTGTCTTAACAGTC | 55632 |
rs769618492 | snp | C/T | 1.7748e-05 | 0.00297887 | intron-variant | G2E3 | GRCh38.p7 | 14:30615581 | AACGATCTCAGAATA[C/T]TTGTTTCAGCATATT | 55632 |
rs769656294 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30563011 | GCCACTACCAGTCTC[C/T]GTGTCTTGGTGATAG | 55632 |
rs769663256 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30600282 | CAGCTCTCCTCATTC[C/T]TGATTCCCTACTCTG | 55632 |
rs769670530 | snp | A/G | 0.00018596 | 0.00964082 | intron-variant | G2E3 | GRCh38.p7 | 14:30590710 | CTAGGGCACAAGGAA[A/G]AACCGTGGGAGAAAG | 55632 |
rs769728699 | snp | A/T | | | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558576 | TTGCCTTCTAACACC[A/T]TCAAATAGTTTATTT | 55632 |
rs769759019 | snp | A/G | 1.66087e-05 | 0.00288168 | intron-variant | G2E3 | GRCh38.p7 | 14:30589369 | TTATTTTCTAATTGA[A/G]AATATATTCATAGTT | 55632 |
rs769767816 | snp | C/T | 1.68252e-05 | 0.0029004 | intron-variant | G2E3 | GRCh38.p7 | 14:30601975 | ATATCTCTATTATGC[C/T]AACATGGAAATTTAA | 55632 |
rs769814878 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30590064 | CATTTGTGCATCTTC[G/T]ATATAACAGCCACTA | 55632 |
rs769828044 | snp | A/G | 1.66051e-05 | 0.00288137 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30593593 | GTTATAACATATTAC[A/G]AAGTCCTTGTTGTAA | 55632 |
rs769839577 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30615749 | AATTTATATTTTGTA[A/G]TTTTTTTCTCTAGAT | 55632 |
rs769904110 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30569978 | AATATCACCACCTCT[A/G]TAAGGCTACACTGCA | 55632 |
rs769907590 | snp | A/T | 1.7809e-05 | 0.00298398 | missense, intron-variant | G2E3 | GRCh38.p7 | 14:30605587 | AAAACTAAAAGATTG[A/T]ATATCAACAAAGCCA | 55632 |
rs769914027 | snp | C/T | 1.83337e-05 | 0.00302762 | intron-variant | G2E3 | GRCh38.p7 | 14:30592492 | TTCAGTGTTAAAGAA[C/T]AGTGGAAAATACATA | 55632 |
rs770032844 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30602624 | TTTTCTTTTTTCTTT[G/T]TTTTAGAAATAAAGT | 55632 |
rs770050956 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30573750 | TCAGTGGACTAGCTA[A/G]TGTCTACCCACGCTG | 55632 |
rs770063685 | in-del | -/AAAG | | | intron-variant | G2E3 | GRCh38.p7 | 14:30599660 | ATTTTAATACGACTT[-/AAAG]AACTTACATGACCAA | 55632 |
rs770085123 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30590987 | ACCCAAAATGTTCCA[A/G]TGAGCATTTCCTTTG | 55632 |
rs770125429 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30604195 | AGGAGCAAGGAATCA[A/G]CCTGCTATAAAAAAG | 55632 |
rs770130133 | in-del | -/TGTGTG | | | intron-variant | G2E3 | GRCh38.p7 | 14:30563696 | TAACTTTGTTACTTT[-/TGTGTG]TGTGTGTGTGTGTGT | 55632 |
rs770133398 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30583696 | TGTGAAGTAATGCAT[A/G]TGATAATTAGCTCCA | 55632 |
rs770140150 | snp | C/T | 3.50982e-05 | 0.00418902 | intron-variant | G2E3 | GRCh38.p7 | 14:30605485 | GTACTTATCTCTATA[C/T]TTAAATTCATGTTTT | 55632 |
rs770183580 | in-del | -/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30573892 | GGCGTCCTGTGGCCT[-/G]GTAAAGGTAACACAT | 55632 |
rs770227856 | snp | C/T | 1.66341e-05 | 0.00288388 | synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616447 | CATCACCAATACATA[C/T]AAAGAGTTTCAAGAA | 55632 |
rs770233784 | snp | A/G | 1.66156e-05 | 0.00288228 | intron-variant | G2E3 | GRCh38.p7 | 14:30581050 | TTTTACAATTAAGAT[A/G]ACTGTATTAATGTTA | 55632 |
rs770263927 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30595837 | TTGGGATTTTGGGAG[A/G]AGAGACTAGAGATTG | 55632 |
rs770322024 | snp | A/G | 1.64743e-05 | 0.00287 | missense, intron-variant, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30598554 | AGCGTTGTGATGTTC[A/G]AAGATGTCGTTGCAA | 55632 |
rs770361487 | snp | C/T | 1.64833e-05 | 0.00287078 | intron-variant | G2E3 | GRCh38.p7 | 14:30601767 | TTTTCTTTGTGTCCT[C/T]AGCAAATGGGAAATA | 55632 |
rs770361705 | snp | C/G | 1.65679e-05 | 0.00287814 | intron-variant, missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30581098 | AATGAAAGTAAACCT[C/G]GTGACTCACAGAACC | 55632 |
rs770478137 | snp | C/T | 1.64743e-05 | 0.00287 | synonymous-codon, intron-variant, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30598594 | AGACTATAATGCACC[C/T]GATAGGTATTTCTGA | 55632 |
rs770491147 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30610674 | AGATGGATAAGGGTT[A/G]GAGTATATACAAGTT | 55632 |
rs770532732 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30583749 | CATATATCAAAACAT[C/T]GTGCTAAACATTGTA | 55632 |
rs770533056 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30597650 | ATTTCAAATGGTGAA[A/G]TGCAAAACCTTCTCC | 55632 |
rs770559741 | in-del | -/ATT | | | intron-variant | G2E3 | GRCh38.p7 | 14:30595628 | AAATATCACTAAGCA[-/ATT]ATTATTATACTCGAT | 55632 |
rs770570188 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30567175 | CTTTGGTATCGGGGT[A/G]TTGGTGGCTTCATAA | 55632 |
rs770576561 | snp | C/G | 1.64781e-05 | 0.00287033 | intron-variant | G2E3 | GRCh38.p7 | 14:30612152 | TATCATTTGAAATGT[C/G]CATGTCACTCAAAAG | 55632 |
rs770623282 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30566410 | TATTTACAGTTCTTT[A/T]ATTTCTTTCAGCACT | 55632 |
rs770647792 | snp | A/T | | | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30601889 | GGGGTATTATCTACA[A/T]TTCAGGTAATTTTTT | 55632 |
rs770657236 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30568911 | TTTCCTCGTATGGCT[C/T]TGACTTACTGTCTGG | 55632 |
rs770747750 | snp | A/G | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30577728 | TGTCATTTCTGCCAC[A/G]GTCTTTTTTGTTGAA | 55632 |
rs770769074 | snp | A/G | 3.95844e-05 | 0.00444866 | intron-variant | G2E3 | GRCh38.p7 | 14:30605455 | TAACTGCTGTTTCAC[A/G]TAAAGTACTTTAAAG | 55632 |
rs770838562 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30588153 | TTATAAGTTACAGAC[G/T]ATTATGTTTTGCAGT | 55632 |
rs770840784 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30589994 | TATATTCAGTACCCT[G/T]TTCTATTCTCTAGGA | 55632 |
rs770872191 | in-del | -/ATTT | | | intron-variant | G2E3 | GRCh38.p7 | 14:30565460 | CTTTGGTAAAGTTCA[-/ATTT]ATTTTTTTCTTGTTG | 55632 |
rs770896268 | snp | A/G | 0.000557673 | 0.0166891 | intron-variant | G2E3 | GRCh38.p7 | 14:30590736 | GAAAGGTGAGCATGA[A/G]TCTAAGGACTACGTG | 55632 |
rs770946537 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30581208 | GAATGAATTCCCTGG[C/T]ACAAGCTTAGTTTGT | 55632 |
rs770967781 | snp | A/G | 9.8974e-05 | 0.007034 | synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30601875 | GTGTTTGGAATGTAG[A/G]GGTATTATCTACAAT | 55632 |
rs771035545 | snp | G/T | | | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558642 | TTTTGGCTGAATACG[G/T]GTGAACTTGGCTTTT | 55632 |
rs771046804 | snp | C/T | 3.35115e-05 | 0.00409324 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30593635 | TTCATAGAGACTGTT[C/T]ACAGGTAAGATACAT | 55632 |
rs771053432 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30609697 | CTAACATGTTTAAGA[G/T]AAAAATAGTATTTTT | 55632 |
rs771151980 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30579014 | GTCTTAGATGTATCA[A/G]CATGTTTAAAATGAT | 55632 |
rs771226632 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30561077 | AGGATTGAATGAGTT[A/G]ATATATACAAAGACC | 55632 |
rs771229215 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30562854 | TGGTGTAAGCTGTCT[C/G]TCTCTCTGCCTCGGC | 55632 |
rs771249759 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30591866 | ATCCACTGTAGGTGT[C/T]TCAACACTTTTTCAT | 55632 |
rs771262088 | snp | A/G | 2.55405e-05 | 0.00357346 | intron-variant | G2E3 | GRCh38.p7 | 14:30593436 | CAAGTTTTGCTTTGC[A/G]GTTCATGAGATTTTT | 55632 |
rs771296377 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30604383 | GAAAATGATCCATGG[A/G]CATTGCCCAAAACAA | 55632 |
rs771356730 | snp | C/T | 1.69795e-05 | 0.00291367 | missense, intron-variant | G2E3 | GRCh38.p7 | 14:30605762 | AACATCTTGAGAACT[C/T]ATCATTGTTTGAAGG | 55632 |
rs771383775 | snp | A/T | | | downstream-variant-500B | G2E3 | GRCh38.p7 | 14:30620241 | TTTCTATAAATTTAT[A/T]GCCCACATTCTGTGC | 55632 |
rs771416186 | snp | C/G | 1.72776e-05 | 0.00293913 | utr-variant-5-prime, missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30586741 | TTCTGTCGAAAACAT[C/G]ATGACTGTCCTAATA | 55632 |
rs771436671 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30619188 | TAATTTGAGGAAGTG[A/T]CTTTTTTTGTTTGGG | 55632 |
rs771444550 | snp | A/G | 1.74449e-05 | 0.00295332 | missense, intron-variant | G2E3 | GRCh38.p7 | 14:30605594 | AAAGATTGTATATCA[A/G]CAAAGCCAATATCTG | 55632 |
rs771447296 | snp | C/G | 3.35312e-05 | 0.00409444 | intron-variant | G2E3 | GRCh38.p7 | 14:30589336 | TATTTTTTTAATGCC[C/G]AACTAGTTTCTTAGA | 55632 |
rs771456742 | in-del | -/TGAT | 1.73276e-05 | 0.00294338 | intron-variant | G2E3 | GRCh38.p7 | 14:30593668 | TTTGTAAGCTTTCTC[-/TGAT]TGATATAAAATTATG | 55632 |
rs771564966 | in-del | -/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30580634 | TAGAAATTTCCTTGA[-/T]TTGACATAGGAGTTG | 55632 |
rs771595256 | snp | A/G | | | upstream-variant-2KB, intron-variant | SCFD1, G2E3 | GRCh38.p7 | 14:30620546 | AGATTCCTTCAAAAT[A/G]TTAGTAATAGTACTG | 55632 |
rs771659995 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30568633 | AACAACCTAGTTTGA[A/G]TTAATACCCACTCAG | 55632 |
rs771699632 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30598834 | TATTTTCTAGAGCCA[C/T]ACTGTCCTATCTGGT | 55632 |
rs771705060 | snp | C/G | 3.29495e-05 | 0.00405877 | intron-variant | G2E3 | GRCh38.p7 | 14:30598608 | CTGATAGGTATTTCT[C/G]AAAGTTCAGTTGTGC | 55632 |
rs771711338 | in-del | -/AA | | | intron-variant | G2E3 | GRCh38.p7 | 14:30562434 | AAGTGACCAGAAGAC[-/AA]GTGTGAGCCTTCTGT | 55632 |
rs771742902 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30586522 | GTGAAATTCATCATT[A/G]AAGACTGGTGAAGAA | 55632 |
rs771793142 | snp | C/T | 1.6517e-05 | 0.00287372 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30612277 | ACTACCTTGAGTTAA[C/T]TGGATGTCTCAGACT | 55632 |
rs771918397 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30567324 | GTTGGGAGGTTCTTC[A/G]TTAGTGATTCAATCT | 55632 |
rs771930939 | snp | C/T | 5.39088e-05 | 0.00519148 | intron-variant | G2E3 | GRCh38.p7 | 14:30612422 | CTTTCAAATTACATG[C/T]TTAAAGTGGTTAATT | 55632 |
rs771956583 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30578076 | AAATTATGAAATTCA[A/G]CTGAAATATGTGAAT | 55632 |
rs771980427 | snp | A/G | 1.81046e-05 | 0.00300865 | intron-variant | G2E3 | GRCh38.p7 | 14:30592476 | CTGTTAAATATGAAA[A/G]TTCAGTGTTAAAGAA | 55632 |
rs772022032 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30600361 | TTAAATTTAATGCTA[C/T]TAAACCAAAAATTCT | 55632 |
rs772130891 | snp | C/G | 3.30327e-05 | 0.0040639 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30602091 | TCATCACCTAAATTA[C/G]CCAGACAGTCACCTG | 55632 |
rs772168360 | snp | C/T | 3.49302e-05 | 0.00417898 | intron-variant | G2E3 | GRCh38.p7 | 14:30616247 | GATTTACTTTTGTTT[C/T]TTTTACTCTTTTATT | 55632 |
rs772252500 | snp | C/G | 1.64966e-05 | 0.00287194 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30615466 | AAAAATCCTTAGTGA[C/G]CTTTTTACAGTACAC | 55632 |
rs772255779 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30617288 | TGCACAAATTTTCTG[C/G]AATCTATGGACATTC | 55632 |
rs772264954 | in-del | -/CT | 3.4114e-05 | 0.00412987 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616584 | AGCTGCTATTGATAA[-/CT]CTCTTTTATTTCACT | 55632 |
rs772274013 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30570012 | GTGTGAAATATTTGT[G/T]TACTTGCCTGCCTCC | 55632 |
rs772292510 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30604239 | GAATTATCTTACTTC[C/T]AAAGGACTTTCGCTT | 55632 |
rs772334024 | in-del | -/TCCCTTTCCCCGGGGGAGTT | | | intron-variant | G2E3 | GRCh38.p7 | 14:30562601 | CCGGGAAAGGGAGTC[-/TCCCTTTCCCCGGGGGAGTT]TAGAGAAGACTCTAC | 55632 |
rs772375982 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30615891 | TCTTCACCCACTGGT[C/T]AGGGCTATAACAATG | 55632 |
rs772392547 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30581335 | ATATAAGATATGGTT[C/G]GTATCTCAATAAAAC | 55632 |
rs772495820 | snp | A/G | 1.65059e-05 | 0.00287275 | synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30597443 | AATAAATGCGGGAGT[A/G]TTTTTCTTTAGGTGT | 55632 |
rs772515109 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30591998 | GATTTCAATGAGGTG[A/T]TTATGTATATAGCTT | 55632 |
rs772518877 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30608131 | TCTTTTAATGTAAAT[C/G]ACTGATCTGCAATAA | 55632 |
rs772531945 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30566291 | CAAAAAAAGGCCATC[A/G]GGATTTTGACAGGAA | 55632 |
rs772585677 | snp | C/T | 1.69908e-05 | 0.00291463 | intron-variant | G2E3 | GRCh38.p7 | 14:30593650 | TACAGGTAAGATACA[C/T]ATTTTGTAAGCTTTC | 55632 |
rs772593371 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30582607 | AATTCTCTTTCTCTT[C/G]AGCTTTATGCACACT | 55632 |
rs772616867 | in-del | -/AGTG | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30577679 | CATGTGATCCATGAT[-/AGTG]AGGAGGAAGTCACAA | 55632 |
rs772673592 | snp | G/T | 2.31361e-05 | 0.0034011 | intron-variant | G2E3 | GRCh38.p7 | 14:30605818 | AATTCTCAAGGTAAT[G/T]ATTTTATTTATTGTT | 55632 |
rs772692046 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30606792 | CAACAATTTAAAAAT[A/T]AAGGAAAAATTTACT | 55632 |
rs772723541 | snp | A/G | 1.64993e-05 | 0.00287218 | synonymous-codon, intron-variant, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30598501 | TGCTTCCTGGGAATT[A/G]GAGGAAAACGCTTAT | 55632 |
rs772751090 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30575522 | GAGTCCTAGCCAGAG[C/G]AGTCAGGCAAGAGAA | 55632 |
rs772811652 | snp | A/C | 1.78198e-05 | 0.00298489 | intron-variant | G2E3 | GRCh38.p7 | 14:30612126 | AAGAAATTTGAGTAT[A/C]AATTAACAAGTATCA | 55632 |
rs772846931 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30595841 | GATTTTGGGAGAAGA[C/G]ACTAGAGATTGCTAT | 55632 |
rs772872335 | in-del | -/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30610122 | CTTCATGGCTTTATC[-/T]ACTCCAGTTTCTGTA | 55632 |
rs772900197 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30595063 | GAATCGCTTGAACCC[A/G]GGAGGTAGAGGTTGC | 55632 |
rs772904346 | snp | C/G | 1.65732e-05 | 0.00287859 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30608004 | TGCCTTGTTTATGGA[C/G]CAGAAAATACCCAGC | 55632 |
rs772988137 | snp | A/G | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30576685 | TTCTTTATTATGTAT[A/G]GGACATCCATAGACA | 55632 |
rs773033577 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30609620 | TGATTTACAGACCTG[C/T]ATTTTTGAGCCCCCG | 55632 |
rs773064962 | snp | G/T | 1.67005e-05 | 0.00288963 | intron-variant | G2E3 | GRCh38.p7 | 14:30601995 | TGGAAATTTAAATCT[G/T]TAGGAGAGTTCCAAA | 55632 |
rs773224943 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30610450 | GAAACCCCATCTTTA[C/T]TAAAAATACAAAAAA | 55632 |
rs773233955 | snp | A/T | 1.65976e-05 | 0.00288072 | intron-variant | G2E3 | GRCh38.p7 | 14:30589371 | ATTTTCTAATTGAGA[A/T]TATATTCATAGTTGA | 55632 |
rs773349603 | snp | A/G | 1.69706e-05 | 0.0029129 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30592416 | TGTGGACTTCAGAGA[A/G]AATGTATTTTCCAGT | 55632 |
rs773386258 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30604230 | GTTTCTGAAGAATTA[C/T]CTTACTTCCAAAGGA | 55632 |
rs773418439 | snp | C/T | 3.30846e-05 | 0.00406709 | synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30612317 | ATTAAGTGATAAATA[C/T]ATGTTAGTAAAAGAC | 55632 |
rs773422415 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30604826 | TAAACTACAATTAAG[A/G]AAGTTAATTATAGCC | 55632 |
rs773437592 | snp | A/G | 2.66628e-05 | 0.00365112 | missense, intron-variant | G2E3 | GRCh38.p7 | 14:30605510 | TGTTTTATAGGCAAG[A/G]CAGCAAATTTAGAAG | 55632 |
rs773496005 | in-del | -/GTGA | | | intron-variant | G2E3 | GRCh38.p7 | 14:30563737 | TGTGTGTGTGTGTGT[-/GTGA]TATAGAGTCTCACTC | 55632 |
rs773527696 | snp | A/G | 1.77489e-05 | 0.00297895 | missense, intron-variant | G2E3 | GRCh38.p7 | 14:30605588 | AAACTAAAAGATTGT[A/G]TATCAACAAAGCCAA | 55632 |
rs773554744 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30559875 | ATATTTTTCTTTCAC[C/G]GTTGACATTTTTCAT | 55632 |
rs773570070 | snp | A/G | 4.97088e-05 | 0.00498517 | intron-variant, missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30581083 | TTTCCTAGTAAAATG[A/G]ATGAAAGTAAACCTG | 55632 |
rs773605188 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30571471 | TTTTGATGTTTAATT[C/T]ATCAGTGTTTTTTAT | 55632 |
rs773626616 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30619140 | ATCTCACCAGAAACT[C/T]ACAATTTTATACTTT | 55632 |
rs773647604 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30590413 | GTCATTAGGCTCAAA[C/G]GTCCAAATTTTTCAA | 55632 |
rs773685019 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30602725 | CAAGTGATCCTCCCA[C/G]CTGAGCCTACCAAGT | 55632 |
rs773731726 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30572800 | GTTTATGTGTTGTTT[C/T]TAATTCTTACAATAA | 55632 |
rs773740170 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30617809 | ACAATGTGAAAATAT[A/G]TAGTCCCATAGTCAT | 55632 |
rs773790376 | snp | C/T | 0.000365831 | 0.0135197 | synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616471 | TCAAGAAAATATGGA[C/T]TTCACCATAAGAAAC | 55632 |
rs773791255 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30583706 | TGCATATGATAATTA[A/G]CTCCATTTAGCTGTT | 55632 |
rs773798189 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | G2E3 | GRCh38.p7 | 14:30619291 | TTTTCCCCTAATTAT[A/G]TGGAAGCTATTGGAA | 55632 |
rs773865583 | snp | C/G | 1.65732e-05 | 0.00287859 | intron-variant, missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30581103 | AAGTAAACCTGGTGA[C/G]TCACAGAACCTTGGT | 55632 |
rs773885640 | in-del | -/ATAA | | | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30617617 | TTATATAAGCAATGT[-/ATAA]ATAAAGTAAAAAGGA | 55632 |
rs773888681 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30578660 | CCTTTATAAATTAAA[C/T]TTTTTATGTTTAAGT | 55632 |
rs773921960 | snp | A/G | 1.6519e-05 | 0.00287388 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30612259 | TAATAAATGAATGCT[A/G]TAACTACCTTGAGTT | 55632 |
rs773922617 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30618033 | AAGAAAAATCATTAC[A/G]TTATTGATATTTTTT | 55632 |
rs773951570 | snp | G/T | 1.64743e-05 | 0.00287 | missense, intron-variant, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30598595 | GACTATAATGCACCT[G/T]ATAGGTATTTCTGAA | 55632 |
rs773998300 | snp | C/G | 1.66466e-05 | 0.00288496 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616490 | ACCATAAGAAACACT[C/G]TAAGACTAGAAAAGG | 55632 |
rs774000115 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30567201 | CATAAAATGAGTTAG[A/G]AAGTGTCATAATATC | 55632 |
rs774032938 | snp | C/T | 9.89234e-05 | 0.0070322 | synonymous-codon, intron-variant, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30598510 | GGAATTAGAGGAAAA[C/T]GCTTATCAAGAGCTT | 55632 |
rs774059585 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30563586 | CATGAAAATGGACAT[A/G]TGGAGCCAATGGGTG | 55632 |
rs774122402 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30566472 | CCACCATGGTTAAAT[G/T]TATTACTAAGTAATT | 55632 |
rs774173366 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30590198 | GCATTAATGATTTTC[A/G]TGGGGGAGCATTTTG | 55632 |
rs774178280 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30596222 | TCTCTCTTCACCATC[C/T]GTAAATCATTCCCCA | 55632 |
rs774184955 | snp | A/G | 1.75326e-05 | 0.00296074 | intron-variant | G2E3 | GRCh38.p7 | 14:30612154 | TCATTTGAAATGTGC[A/G]TGTCACTCAAAAGTA | 55632 |
rs774228052 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30595188 | GAAATATTAGAAATT[C/T]GGTTAATACTTGCAA | 55632 |
rs774281755 | snp | C/T | 4.94882e-05 | 0.0049741 | synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30615463 | TGCAAAAATCCTTAG[C/T]GAGCTTTTTACAGTA | 55632 |
rs774294614 | snp | C/G/T | 5.01377e-05 | 0.00500667 | missense, synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30592397 | ACGAAGTTATCATTT[C/G/T]CCATGTGGACTTCAG | 55632 |
rs774340974 | in-del | -/ATTATTC | | | intron-variant | G2E3 | GRCh38.p7 | 14:30600451 | GATCTAGTGACCCTG[-/ATTATTC]ATTCGTTAACACCAA | 55632 |
rs774446765 | in-del | -/TCAT | | | intron-variant | G2E3 | GRCh38.p7 | 14:30615241 | GTTGTTTTTTAAAAA[-/TCAT]TCATTAGCTGTTTTG | 55632 |
rs774513318 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30591873 | GTAGGTGTCTCAACA[C/T]TTTTTCATTTGGTCA | 55632 |
rs774522929 | snp | C/T | | | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30557796 | ACAGATTATTTTCTA[C/T]CTTCCACTGTTAAAA | 55632 |
rs774527521 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30581242 | TCCACATACTAAAGT[A/G]TAATATTGCATATAT | 55632 |
rs774561099 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30569993 | GTAAGGCTACACTGC[A/T]TGTGTGTGAAATATT | 55632 |
rs774570326 | snp | A/T | 4.06215e-05 | 0.00450656 | intron-variant | G2E3 | GRCh38.p7 | 14:30615309 | TATAATACCAAACAC[A/T]CATGTATGAATGTTG | 55632 |
rs774593357 | snp | C/G/T | 7.61206e-05 | 0.00616891 | intron-variant | G2E3 | GRCh38.p7 | 14:30593438 | AGTTTTGCTTTGCAG[C/G/T]TCATGAGATTTTTTT | 55632 |
rs774616065 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30569113 | AAATATATTTTAAGT[A/T]CATAATTATGTTCAT | 55632 |
rs774717478 | snp | A/G | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30576274 | AGCAATAGGGAAAAG[A/G]CTCTCTGTTTATTAA | 55632 |
rs774750248 | in-del | -/TT | 1.65293e-05 | 0.00287479 | intron-variant | G2E3 | GRCh38.p7 | 14:30597401 | TCATTAACAGTAGAC[-/TT]TTTATTTTCCACTGT | 55632 |
rs774751885 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30606091 | TTATCTTAACTCTAA[C/T]TTCATTTTAATAGAG | 55632 |
rs774806797 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30604399 | CATTGCCCAAAACAA[A/G]ATTATTTTTGAGAAC | 55632 |
rs774856720 | snp | C/T | 1.67172e-05 | 0.00289108 | stop-gained, intron-variant | G2E3 | GRCh38.p7 | 14:30605638 | GATGCATTCAGAAAT[C/T]GAAACTTTAATCCTT | 55632 |
rs774871574 | snp | C/T | 1.7426e-05 | 0.00295173 | synonymous-codon, intron-variant | G2E3 | GRCh38.p7 | 14:30605781 | ATTGTTTGAAGGGTC[C/T]TTGTCAAAGAACTTG | 55632 |
rs774906986 | snp | C/T | 1.70988e-05 | 0.00292389 | utr-variant-5-prime, missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30586750 | AAACATGATGACTGT[C/T]CTAATAAATACGGAG | 55632 |
rs774938205 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30574255 | AACCTAAATATGGAT[A/G]CCAATTTCAGGAAAC | 55632 |
rs774959349 | snp | C/T | 1.70557e-05 | 0.0029202 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30586755 | TGATGACTGTCCTAA[C/T]AAATACGGAGAAAAG | 55632 |
rs774961490 | snp | C/T | 1.71711e-05 | 0.00293006 | synonymous-codon, intron-variant | G2E3 | GRCh38.p7 | 14:30605601 | GTATATCAACAAAGC[C/T]AATATCTGGAATAGT | 55632 |
rs775028944 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30604086 | AATATTGAGATTTCC[A/C]AAGACGCTACACCAG | 55632 |
rs775042994 | snp | C/T | 3.29652e-05 | 0.00405974 | synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30601809 | GTGTTGTGGTTCCAG[C/T]GGCACACATTTAGCC | 55632 |
rs775075872 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30584064 | ACTAATCTGCTTTTT[A/G]TGTGTCCCTGTGGAT | 55632 |
rs775123300 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30561573 | GAATTCTCCAAATCT[A/G]TCTCTTATTACATTT | 55632 |
rs775131534 | in-del | -/TTG | | | cds-indel, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30617398 | TTTAATCATGGGAAA[-/TTG]TTGTTGTTGTTGTTG | 55632 |
rs775183400 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | G2E3 | GRCh38.p7 | 14:30619465 | GTGATTATCATGTAC[C/T]GCATTGTTACTTTAA | 55632 |
rs775192800 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30587745 | GTAAATAAGGCTACT[C/T]GTGGCATGGCATCTG | 55632 |
rs775251004 | snp | A/G | 1.67511e-05 | 0.00289401 | intron-variant | G2E3 | GRCh38.p7 | 14:30581150 | AATAATTTTATTACA[A/G]TGAGTGTTTTAAATA | 55632 |
rs775305327 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30579052 | AGATTGTGATCCTCA[A/G]TCAATTTGTTCACTT | 55632 |
rs775320535 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30611685 | TTTTAAGAGATAAGG[C/T]CTCAGTCTGTCACCC | 55632 |
rs775339331 | snp | A/G | 1.64751e-05 | 0.00287007 | intron-variant | G2E3 | GRCh38.p7 | 14:30598612 | TAGGTATTTCTGAAA[A/G]TTCAGTTGTGCTTAG | 55632 |
rs775501762 | snp | G/T | 1.65231e-05 | 0.00287424 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30612292 | TTGGATGTCTCAGAC[G/T]TATAACGACATTAAG | 55632 |
rs775595841 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30590177 | TGTTTAGAGAATGTG[A/T]TACTGGCATTAATGA | 55632 |
rs775615328 | snp | C/G | | | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558703 | TTAAAAGCCCTGACT[C/G]TGCCGGGATAGGACT | 55632 |
rs775619073 | snp | A/T | 0.000173358 | 0.00930855 | intron-variant | G2E3 | GRCh38.p7 | 14:30616252 | ACTTTTGTTTCTTTT[A/T]CTCTTTTATTGGTAA | 55632 |
rs775692906 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30600388 | TTCTTAGAAGGCAGA[G/T]ATCTCATTGAAGGTA | 55632 |
rs775737908 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30570985 | TAACTTTAAGTACAG[A/T]TTATCTTTTTTTGTC | 55632 |
rs775789723 | in-del | -/C | 1.67301e-05 | 0.00289219 | intron-variant | G2E3 | GRCh38.p7 | 14:30597558 | TTATGATAAAAAAAA[-/C]GATATTTTAAATGTA | 55632 |
rs775811263 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30581165 | ATGAGTGTTTTAAAT[A/G]TGTTACTTAAACATT | 55632 |
rs775880292 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30592936 | GTTTTATGAATTTTG[A/G]CTTTTGGTATCATAA | 55632 |
rs775953965 | in-del | -/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30591074 | TTTTGGATTAAGGGA[-/T]ATTCAACCTGTACTT | 55632 |
rs776003343 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30592000 | TTTCAATGAGGTGTT[C/T]ATGTATATAGCTTTT | 55632 |
rs776008644 | snp | A/G | 4.95193e-05 | 0.00497566 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30597454 | GAGTGTTTTTCTTTA[A/G]GTGTACAATATGCAA | 55632 |
rs776063581 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30608394 | TGAGGCAGATTCCCT[A/G]TTGCAAGCTAGAAAG | 55632 |
rs776077778 | snp | A/C | 2.93621e-05 | 0.00383147 | intron-variant | G2E3 | GRCh38.p7 | 14:30605842 | TATTGTTGTATATAC[A/C]AAATATCACATGTAT | 55632 |
rs776098583 | snp | A/G | 5.10347e-05 | 0.00505121 | intron-variant | G2E3 | GRCh38.p7 | 14:30593651 | ACAGGTAAGATACAT[A/G]TTTTGTAAGCTTTCT | 55632 |
rs776106447 | snp | C/T | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30576550 | TTAAGGGTTTCTGCA[C/T]AGCAAAAGAAACTAC | 55632 |
rs776113971 | snp | A/T | 0.000162129 | 0.00900212 | intron-variant | G2E3 | GRCh38.p7 | 14:30605820 | TTCTCAAGGTAATTA[A/T]TTTATTTATTGTTGT | 55632 |
rs776143410 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30562923 | GACCCACGTGAACTT[A/T]CCTATCATTGGAGAT | 55632 |
rs776187792 | snp | C/T | 1.65091e-05 | 0.00287303 | synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30607979 | TTTCTTTTCTAAAAC[C/T]TTGTTTAACTGCCTT | 55632 |
rs776256658 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30564506 | ACTGGCTAATTAAAA[A/T]TTTTTTTTATAGAGA | 55632 |
rs776300437 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30599478 | GTGATCTGCCCGCCT[C/T]GGCCTCCCAAAGTGC | 55632 |
rs776318296 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30606544 | ATGTAAAAATAAAGA[A/G]AAAACTTTCCAAATA | 55632 |
rs776341966 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30585421 | ATGAGACTATTCTTT[C/T]ACCATTGAATGGTCT | 55632 |
rs776358546 | snp | A/G | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30575843 | TACAATGAGAATTAC[A/G]AAGCACTGCTCAAAG | 55632 |
rs776459032 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30599013 | CTCATAATTTTAGAG[G/T]CTGGAAGTTTAAGAT | 55632 |
rs776469016 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30560461 | CTTCCTGCTATTGAA[C/T]TTTTAAGTGTTAGCC | 55632 |
rs776503544 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30609825 | TGGAGAGTCATTTTC[A/T]TACTCCTCCATTTTC | 55632 |
rs776585097 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30598292 | TTGGGAGGCTGAGGC[A/G]GGGAGAATCGCTTGA | 55632 |
rs776674525 | snp | A/C | 1.6486e-05 | 0.00287102 | synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30601830 | ACATTTAGCCTGCTC[A/C]TCATTACGGTCATGG | 55632 |
rs776701617 | snp | A/T | 1.68952e-05 | 0.00290642 | synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30592409 | TTTCCCATGTGGACT[A/T]CAGAGAGAATGTATT | 55632 |
rs776761760 | snp | A/T | 2.04034e-05 | 0.00319394 | intron-variant | G2E3 | GRCh38.p7 | 14:30615304 | CCTAATATAATACCA[A/T]ACACACATGTATGAA | 55632 |
rs776772484 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30578118 | TTTTTACTAAGGTTT[C/T]GTTTTGGAGACTTGT | 55632 |
rs776791482 | snp | C/T | 1.65792e-05 | 0.00287912 | intron-variant | G2E3 | GRCh38.p7 | 14:30592272 | GTCTTGATCATATTA[C/T]AATACTCAGATTTTT | 55632 |
rs776804242 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30617596 | ATTGCTCTTGAATGA[C/T]ATCTGTTATATAAGC | 55632 |
rs776854173 | snp | A/C | 3.36327e-05 | 0.00410063 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616278 | GGTAAATTTTTTCAG[A/C]TGGTAAATCTACAAC | 55632 |
rs776863306 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30559563 | ACGCATCCTCCGTGG[C/G]TTTTTTTAAACCCGT | 55632 |
rs776915453 | in-del | -/TT | | | intron-variant | G2E3 | GRCh38.p7 | 14:30607701 | ACAATAGATTTTTAC[-/TT]TTTATATTCAGAAAA | 55632 |
rs776933398 | in-del | -/TGC | | | intron-variant | G2E3 | GRCh38.p7 | 14:30604583 | CAAGTTCTGGGGTAA[-/TGC]TGCTGCTGCTGCTGC | 55632 |
rs776940662 | in-del | -/TT | | | intron-variant | G2E3 | GRCh38.p7 | 14:30563049 | CCGGGCCCAGCTGTC[-/TT]TTCTTTTATCTCTTT | 55632 |
rs776959368 | snp | A/C | 1.66338e-05 | 0.00288386 | synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616426 | TAATAACTGTTTAGC[A/C]ATTCCCATCACCAAT | 55632 |
rs776967449 | in-del | C/TGCGTGTGTGT | | | intron-variant | G2E3 | GRCh38.p7 | 14:30573430 | GTGTGTGTGTGTGTG[C/TGCGTGTGTGT]GTGTCTCTGTGTGTG | 55632 |
rs777023063 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30582388 | TATAAAAATGCATGC[C/T]TGAAACCTAGTCTGT | 55632 |
rs777026262 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30602282 | ATTTGATCATGAAAT[C/G]AATGCAACCAGCATT | 55632 |
rs777118682 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30616206 | TATTTGGAGAAGAAT[A/C]TATGATGATAGCAAT | 55632 |
rs777205033 | in-del | -/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30559943 | TGGTAACAGCGGTGG[-/T]TGATTAACTAGGGTC | 55632 |
rs777231013 | snp | A/G | 1.65263e-05 | 0.00287452 | synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30597488 | TAGTGACATCTTTCA[A/G]AAAGAGATGTTGAGA | 55632 |
rs777350607 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30611585 | CATCTTTTAATTCTC[A/G]GCTGTTACTCTTTTT | 55632 |
rs777380314 | in-del | -/C | 1.73667e-05 | 0.0029467 | intron-variant | G2E3 | GRCh38.p7 | 14:30612391 | AAAGGTAAGTTGTTT[-/C]TATTAATATATGGCT | 55632 |
rs777422464 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30603124 | CGAGGTCAAGAGATC[A/G]AGAACATCCTGGCCA | 55632 |
rs777441962 | snp | A/C | 1.74531e-05 | 0.00295402 | intron-variant | G2E3 | GRCh38.p7 | 14:30602178 | AATCTATTTGGAGAA[A/C]ATTATGATAGGAAAT | 55632 |
rs777529895 | snp | A/G | 1.66324e-05 | 0.00288374 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616388 | GAGTGTCTGCATGTG[A/G]ATTTTCCTGTTGGAA | 55632 |
rs777537809 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30589799 | TCAGAATTATGATCA[C/T]AACTCCACTCTGCTG | 55632 |
rs777546858 | snp | A/G | 2.19334e-05 | 0.00331153 | missense, intron-variant | G2E3 | GRCh38.p7 | 14:30605545 | GTATCAACACTATTA[A/G]TAGAGTTAGGATTCC | 55632 |
rs777584106 | in-del | -/T | 0.000298545 | 0.0122141 | intron-variant | G2E3 | GRCh38.p7 | 14:30593446 | TTGCAGTTCATGAGA[-/T]TTTTTTTAAAATAAT | 55632 |
rs777635246 | snp | C/T | 1.65056e-05 | 0.00287272 | synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30592349 | TTGCAAGAAAAATGG[C/T]GCTTCAATTGGATGT | 55632 |
rs777667174 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30564856 | CATTTTGTATATCCA[C/T]TCATCAATTGATGTA | 55632 |
rs777761106 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30607395 | TCTATGGTAAAGCCT[A/G]TTGGTTCTAGACTGC | 55632 |
rs777765795 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30583103 | TGGAGCAGTTAGGGA[C/G]TTTCTGCGGTATGCA | 55632 |
rs777794404 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30617103 | TATATTAAGATGACC[C/T]ACACTGCAATTAGAT | 55632 |
rs777803404 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30563840 | TTCTCCTGCCTCAAC[C/T]TCCTGAGTAGCTGGA | 55632 |
rs777807125 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30571851 | GTCATGAAATCACAT[A/G]GTTGGAGACCACTTT | 55632 |
rs777807186 | snp | C/T | | | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558577 | TGCCTTCTAACACCA[C/T]CAAATAGTTTATTTG | 55632 |
rs777808352 | in-del | -/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30563159 | ACACTCTTGGTACAG[-/T]TTTTTTTTTTTTTTA | 55632 |
rs777916644 | snp | A/T | 2.6112e-05 | 0.00361322 | intron-variant | G2E3 | GRCh38.p7 | 14:30586839 | AATTTATAATTAAAT[A/T]CTAGAAATTTGGTGT | 55632 |
rs777988139 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30573880 | ACCAGATATCTGGGC[A/G]TCCTGTGGCCTGGTA | 55632 |
rs778038115 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30584959 | TCCTCAGCCTCCCGA[A/G]TAGCTGGGATTACAG | 55632 |
rs778049649 | snp | A/G | | | downstream-variant-500B | G2E3 | GRCh38.p7 | 14:30620200 | GGCTATTTGTCTATG[A/G]TTGCTGTTCTTCTGT | 55632 |
rs778063013 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30575233 | GTCTTCTTTTGAGAA[A/G]TATCTGCTTATGTCC | 55632 |
rs778122835 | in-del | -/TTA | | | intron-variant | G2E3 | GRCh38.p7 | 14:30574085 | TAGATTAACCACTCT[-/TTA]TTATTTTCCACATTC | 55632 |
rs778172022 | in-del | -/AGG | | | intron-variant | G2E3 | GRCh38.p7 | 14:30588324 | TTATGCAGTAGAATT[-/AGG]AGAGCCATTTTATGT | 55632 |
rs778230556 | snp | A/G/T | 3.46905e-05 | 0.00416464 | utr-variant-5-prime, missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30586739 | TTTTCTGTCGAAAAC[A/G/T]TGATGACTGTCCTAA | 55632 |
rs778231580 | snp | A/G | 1.64827e-05 | 0.00287073 | intron-variant | G2E3 | GRCh38.p7 | 14:30601760 | GTTCTGCTTTTCTTT[A/G]TGTCCTCAGCAAATG | 55632 |
rs778238453 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30582333 | CAAATTTTAAACATT[A/G]AAAGCAGGAAGGTAC | 55632 |
rs778299651 | snp | A/G | 1.67478e-05 | 0.00289372 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30615377 | CTGAAAACCCTTGGT[A/G]TTTTGGAGAAAATTC | 55632 |
rs778321339 | snp | A/G | 1.64741e-05 | 0.00286998 | missense, intron-variant, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30598563 | ATGTTCGAAGATGTC[A/G]TTGCAAAGAAGGGCG | 55632 |
rs778351619 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30582625 | CTTTATGCACACTTG[C/G]GGGTAAAAGTGTAGG | 55632 |
rs778360552 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30569528 | TGTTAAAATATAATT[A/G]AGGCCTTATTTTTTA | 55632 |
rs778438657 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30579829 | TACCTAGTGGCATTA[C/T]TATGTTTTATTCTTT | 55632 |
rs778445653 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30597257 | GAATTATAGATTTTA[A/G]CAGTGGGATAACTTA | 55632 |
rs778484851 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30568576 | TTTTAGTTATATTCT[C/T]AGTGGCTATCTTGGG | 55632 |
rs778498074 | snp | A/G | 1.64808e-05 | 0.00287057 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30601780 | CTCAGCAAATGGGAA[A/G]TAAAGCGCTGTCAGT | 55632 |
rs778534883 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30613243 | CTTGTTCATCTTTAT[C/T]CTACCCTTGTTATTG | 55632 |
rs778558346 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30598668 | GAGAAAGTAGATTTT[A/G]TAGTTAGTGAAACGT | 55632 |
rs778563014 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30591530 | TTCCTTCTAGAGGCA[C/T]TAAGGGAGAATTGAT | 55632 |
rs778573644 | snp | A/G | 1.79596e-05 | 0.00299658 | intron-variant | G2E3 | GRCh38.p7 | 14:30592466 | AGTTATTTAACTGTT[A/G]AATATGAAAGTTCAG | 55632 |
rs778682128 | snp | C/T | 1.78328e-05 | 0.00298598 | stop-gained, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30593493 | TTTTGTTGGGACCAT[C/T]GACCTGTTCAAATAA | 55632 |
rs778683927 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30594928 | GAGGTCAGGAGTTCG[A/C]GACCAGCATGGCCAA | 55632 |
rs778751833 | snp | A/G | | | | | GRCh38.p7 | 14:30578871 | CACGCTTCTTTCCAT[A/G]TGGATATTCAGTTTT | 55632 |
rs778769231 | snp | A/T | 5.39578e-05 | 0.00519384 | stop-gained, intron-variant | G2E3 | GRCh38.p7 | 14:30605566 | TTAGGATTCCAAATT[A/T]AAAAAAAAACTAAAA | 55632 |
rs778779714 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30559478 | CTCTCGACGGTTGCG[C/T]ACGCCAGCCAGCTCT | 55632 |
rs778780066 | in-del | -/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30563030 | CTTGGTGATAGTGGT[-/C]CCCCCGGGCCCAGCT | 55632 |
rs778799434 | in-del | -/AAGG | | | intron-variant | G2E3 | GRCh38.p7 | 14:30568418 | CATTTAATTACTGTT[-/AAGG]AAGGATTTCTGACAT | 55632 |
rs778843004 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30581963 | ATATTATTCTTACAA[C/T]TCTATATCTTGATCA | 55632 |
rs778848080 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30560669 | TTTTTTTCTACCTGA[A/T]TTATTTTCATTGGAT | 55632 |
rs778861203 | snp | A/C/G | 7.72865e-05 | 0.00621598 | intron-variant | G2E3 | GRCh38.p7 | 14:30605467 | CACATAAAGTACTTT[A/C/G]AAGTACTTATCTCTA | 55632 |
rs778861289 | snp | C/T | 1.68746e-05 | 0.00290466 | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616544 | CATTAAAATGTTTCC[C/T]TGAACAAAGAGAAGC | 55632 |
rs778908170 | in-del | -/TG | | | intron-variant | G2E3 | GRCh38.p7 | 14:30589219 | TCAAACAATGTAAGT[-/TG]AGCCTCTTACTTTGA | 55632 |
rs778915043 | in-del | -/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30590023 | ATAGGCATTCTAAAC[-/T]TTTAACTCCTTGCTC | 55632 |
rs778953457 | snp | A/G | 1.65059e-05 | 0.00287275 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30597429 | CTGTAGGTTCAAGCA[A/G]TAAATGCGGGAGTGT | 55632 |
rs779014084 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30603837 | TGACACAGCAAGACC[C/T]TGTCTCTAAAAAGTT | 55632 |
rs779127343 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30562875 | CTGCCTCGGCTGCCA[A/G]GCAGGGAAGGGCCCC | 55632 |
rs779130199 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30608857 | CGTGGTGGCATGTGC[C/T]TGTAATCCCAGCTAC | 55632 |
rs779136782 | snp | A/G | 1.68343e-05 | 0.00290118 | intron-variant | G2E3 | GRCh38.p7 | 14:30598441 | ATCCTCTTATGTAAC[A/G]TTATTTATAGGTCAA | 55632 |
rs779178280 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30607858 | ATAATAATAGAAGTG[C/T]ATTTGATATATTTTC | 55632 |
rs779207765 | in-del | -/AAT | 1.66225e-05 | 0.00288287 | cds-indel, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30615388 | TGGTGTTTTGGAGAA[-/AAT]TCAGGCTTATCCAGA | 55632 |
rs779211640 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30578338 | AACTCCTATATATCC[G/T]TTATCTAGATTCACT | 55632 |
rs779217017 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30592620 | CATTTCTATGTGCCA[A/C]GTCTTGAGAATTACC | 55632 |
rs779226700 | snp | A/G | 1.7603e-05 | 0.00296668 | intron-variant | G2E3 | GRCh38.p7 | 14:30608077 | TAATCAGGGTAAGCA[A/G]TGTATCTGTTTATTA | 55632 |
rs779284683 | snp | G/T | 8.42197e-05 | 0.00648867 | intron-variant | G2E3 | GRCh38.p7 | 14:30589506 | AAATTATTTTACTAT[G/T]AAGTAATGTCATAAA | 55632 |
rs779316356 | snp | C/T | 4.75308e-05 | 0.00487474 | intron-variant | G2E3 | GRCh38.p7 | 14:30607873 | TATTTGATATATTTT[C/T]ATCTGTATTTACAGC | 55632 |
rs779352682 | snp | A/G | 1.66663e-05 | 0.00288667 | intron-variant | G2E3 | GRCh38.p7 | 14:30601918 | TTTGTAATTTTGAAT[A/G]AAGTTTTTATTCAAA | 55632 |
rs779363391 | in-del | -/CTA | | | intron-variant | G2E3 | GRCh38.p7 | 14:30606430 | TTTCATTTGAATTTC[-/CTA]CTACTATATTTTCTG | 55632 |
rs779394197 | snp | C/G | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30576300 | ATTAAATGGTGCTGG[C/G]ATATCTGGCTAGCCA | 55632 |
rs779438949 | snp | A/G | 3.30814e-05 | 0.00406689 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30602043 | TTACCCAATTCTAAT[A/G]ATGTGGGGATTACAG | 55632 |
rs779473949 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30586616 | TATATGATTTGCTCT[C/G]AGAAAGAATTTAACA | 55632 |
rs779477103 | in-del | -/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30608853 | CAGGCGTGGTGGCAT[-/G]TGCCTGTAATCCCAG | 55632 |
rs779519568 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30587448 | TACATACAGTGTTTC[G/T]TGATACTATATAGTT | 55632 |
rs779568612 | snp | A/G | | | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558208 | TGAGCCACCGCGCCC[A/G]GCCCTCAAACTGTAT | 55632 |
rs779572707 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30586350 | GTAGTTTGTTTCTTC[A/G]TTAAGCATTCTCCTA | 55632 |
rs779605976 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30587620 | CAGCTGAAGACTTTA[C/T]TAGGTTGCAGGATCC | 55632 |
rs779624617 | snp | A/T | 3.33856e-05 | 0.00408555 | intron-variant | G2E3 | GRCh38.p7 | 14:30589353 | ACTAGTTTCTTAGAG[A/T]TTATTTTCTAATTGA | 55632 |
rs779637523 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30569765 | ATTATATTACTTACT[A/C]TCTGATAATCCAATC | 55632 |
rs779806521 | snp | C/T | 0.000120406 | 0.00775813 | intron-variant | G2E3 | GRCh38.p7 | 14:30615554 | GGTATGTGGATATTT[C/T]ATTTTACTTTTAACG | 55632 |
rs779858002 | in-del | -/AAG | 0.000119741 | 0.00773668 | cds-indel, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30586768 | AATAAATACGGAGAA[-/AAG]AAAACTAAGGAGAAA | 55632 |
rs779858875 | snp | A/G | 1.65397e-05 | 0.00287569 | intron-variant | G2E3 | GRCh38.p7 | 14:30597378 | TATCACCTGATAACA[A/G]ATTTAAATCATTAAC | 55632 |
rs779876282 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30568677 | CAAAAATTACACTTC[C/T]GTATATCTCATCCTT | 55632 |
rs779890211 | snp | A/G | 1.65228e-05 | 0.00287422 | synonymous-codon, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30615409 | GGCTTATCCAGAAGC[A/G]TTTTGTAGCATCCTG | 55632 |
rs779973012 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30572045 | ATCTCTTCATTTATT[C/T]AGGTCTTTCATTTCT | 55632 |
rs780003335 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30580166 | GGCAAATGCAACAGC[C/T]ACAAATACGGTATAG | 55632 |
rs780034857 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30562038 | ATTCATGAATTTAAA[A/T]TGCTTTATACATATT | 55632 |
rs780035152 | snp | G/T | 1.66543e-05 | 0.00288563 | missense, intron-variant | G2E3 | GRCh38.p7 | 14:30605702 | ATGATAATTTTGGAA[G/T]TGAGCATCCTGGATC | 55632 |
rs780049300 | in-del | -/ATC | | | upstream-variant-2KB, intron-variant | SCFD1, G2E3 | GRCh38.p7 | 14:30620275 | TGGTCAGGAGTTTTT[-/ATC]ATTTCATATATATGC | 55632 |
rs780111700 | in-del | -/TGTT | | | intron-variant | G2E3 | GRCh38.p7 | 14:30587023 | CCTATCATTATTTCG[-/TGTT]TGTTTGTTTGTTTGT | 55632 |
rs780156751 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30591686 | TCTCCCTCTCCTTTC[C/T]CTTGTAAAGACCTCA | 55632 |
rs780204266 | snp | A/G | 1.65875e-05 | 0.00287984 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30612207 | TCTCCTTCATTACAG[A/G]TAAATACTGCAACAA | 55632 |
rs780213711 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30583282 | TATACTAACATTTGG[C/T]TCTATGTATATGTCA | 55632 |
rs780245317 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30586529 | TCATCATTAAAGACT[A/G]GTGAAGAACATAAAG | 55632 |
rs780270659 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30595651 | TATACTCGATTAGAG[C/T]ATACTAAGGATGGGG | 55632 |
rs780272519 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30582155 | GCCAAATGCAAATAC[A/G]CATCTACTATTGATA | 55632 |
rs780332998 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30609044 | CTCTTATAACTACTA[C/T]ATGTTGTGTCACTTT | 55632 |
rs780336640 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30617334 | TTTTGAGGTGGATAA[A/C]ATTTAGTTGAAAATA | 55632 |
rs780395275 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30594612 | GCGGGAGAATGGCAT[C/G]AACCCGGAAGACGGA | 55632 |
rs780431054 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30589188 | ATACAAACTGATAAT[A/G]TACAGTGCCATCTAA | 55632 |
rs780464187 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30610387 | TTGGGAGAACAGGTG[A/G]GTGGATCACCGGGGT | 55632 |
rs780476529 | snp | A/G | 3.53632e-05 | 0.0042048 | intron-variant | G2E3 | GRCh38.p7 | 14:30608081 | CAGGGTAAGCAATGT[A/G]TCTGTTTATTAAAAT | 55632 |
rs780479943 | snp | C/T | 1.70848e-05 | 0.00292269 | intron-variant | G2E3 | GRCh38.p7 | 14:30589524 | GTAATGTCATAAATA[C/T]TGTCAATACTTGGGA | 55632 |
rs780625181 | in-del | -/GTAA | 3.33195e-05 | 0.0040815 | splice-donor-variant | G2E3 | GRCh38.p7 | 14:30589484 | AGAGCTTCTAAACTG[-/GTAA]GTAAGTAAATTATTT | 55632 |
rs780655213 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30564345 | TTTATAAAATTAGCC[A/G]TTTTATTTGAGACAA | 55632 |
rs780657219 | snp | A/G | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30577063 | AACCCCGTCTGTACT[A/G]AAAATACAAAAATTA | 55632 |
rs780731683 | snp | C/T | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30577371 | GTGTAACAGATAACT[C/T]CAGAACTTGCTGGTT | 55632 |
rs780750823 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30575593 | CTATCTCTTTGCAGA[C/T]TACATGATTCTGTAT | 55632 |
rs780750937 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30606184 | ATAGAGTTTTTATAA[A/C]ATAGTTTCCTGGTCC | 55632 |
rs780776210 | snp | A/G | | | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558300 | TCAATGTTATTAGAT[A/G]TGAGGATGATCTGGT | 55632 |
rs780838538 | snp | A/C | | | intron-variant | G2E3 | GRCh38.p7 | 14:30601177 | GTCATACCCAACAAA[A/C]AGGCTGGAGCCCTAC | 55632 |
rs780848104 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30616807 | TCTCAAAATGGTTGT[A/G]TGGATTTTATTTAGG | 55632 |
rs780967936 | snp | C/G | 0.000186098 | 0.00964441 | intron-variant | G2E3 | GRCh38.p7 | 14:30590673 | CAAGAAGGTAGGAGA[C/G]TTAATGGTAAAAACA | 55632 |
rs780970072 | snp | A/T | 1.71363e-05 | 0.00292709 | intron-variant | G2E3 | GRCh38.p7 | 14:30602163 | GGAGAAATACATAAA[A/T]ATCTATTTGGAGAAA | 55632 |
rs781093839 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30615691 | TATTTCAAAGCAAGT[G/T]TATATGACTGAATTA | 55632 |
rs781099291 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30560799 | GATTCTGAATCAGTA[A/G]GTCTGGAGGATGGCA | 55632 |
rs781147082 | snp | A/G | 3.29962e-05 | 0.00406165 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30615440 | TGTCATAAACCTGAG[A/G]GTCTTTCTGCAAAAA | 55632 |
rs781194475 | in-del | -/TTG | 2.53662e-05 | 0.00356125 | intron-variant | G2E3 | GRCh38.p7 | 14:30605829 | TAATTATTTTATTTA[-/TTG]TTGTATATACCAAAT | 55632 |
rs781227538 | snp | A/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30575105 | TTTTTTGACTTTGTG[A/T]TAATAGCCATTCTGA | 55632 |
rs781234191 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30581781 | TTCCCAAATAGATGC[A/G]GTCCGTTTTGACCTT | 55632 |
rs781238644 | snp | C/G | 6.17506e-05 | 0.00555621 | intron-variant | G2E3 | GRCh38.p7 | 14:30586713 | ATTTACTTTTTCACT[C/G]TTAGCTTGTGTTTTC | 55632 |
rs781245103 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30568193 | TGTAACAATCTTCAA[C/T]TTAAAGCCTGTTTTG | 55632 |
rs781266362 | snp | A/G/T | 7.14252e-05 | 0.00597564 | synonymous-codon, missense, intron-variant | G2E3 | GRCh38.p7 | 14:30605586 | AAAAACTAAAAGATT[A/G/T]TATATCAACAAAGCC | 55632 |
rs781329144 | snp | C/T | 1.64751e-05 | 0.00287007 | intron-variant | G2E3 | GRCh38.p7 | 14:30598647 | TCCTTGTTTAAACCT[C/T]CTGCTGAGAAAGTAG | 55632 |
rs781395614 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30611289 | CCCAATTATTACTCC[A/G]ACAGGGTGTAAAGAT | 55632 |
rs781398008 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30584903 | ACACAATCTTGGCTC[A/G]CCACTGCAACCTCCA | 55632 |
rs781471064 | snp | C/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30604107 | GCTACACCAGGGAAG[C/G]TTGACTCCTTGCTCC | 55632 |
rs781503023 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30566911 | GTTGTATTTTGTCAA[A/G]TGCTTTTTCTGCATC | 55632 |
rs781508182 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30618882 | TTTTAAAAAAGAATT[A/C]TGCTATAAATCTTTA | 55632 |
rs781525170 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30583515 | GCTGGTTACCAGCGG[C/T]TGGGAGGATTGGGAG | 55632 |
rs781576407 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30610486 | CCAGGTGTGGTGGCG[C/T]GCGCCTATAGTCCCA | 55632 |
rs781593004 | snp | A/C | 1.80595e-05 | 0.0030049 | intron-variant | G2E3 | GRCh38.p7 | 14:30608111 | TGCACACTACATTCT[A/C]GGTATCTTTTAATGT | 55632 |
rs781608425 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30597088 | GATGAGGTAACTCAG[A/G]AGTTTCATTTTTTTC | 55632 |
rs781624871 | snp | A/G | 1.64749e-05 | 0.00287005 | missense, intron-variant, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30598550 | TATGAGCGTTGTGAT[A/G]TTCGAAGATGTCGTT | 55632 |
rs781631119 | snp | C/G | 1.65343e-05 | 0.00287521 | missense, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30612229 | CTGCAACAACTGTAG[C/G]TGACTTAAAGTCAAT | 55632 |
rs781691398 | snp | C/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30559326 | GAGAGAGAAGCAGGA[C/T]CGTGGGGTGGGAGAG | 55632 |
rs781699623 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30582840 | GAGGGCAGAGTAGTT[A/G]GGCTATTTCACTATA | 55632 |
rs781755874 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30566194 | GGAATTGGAAAATTT[G/T]AATCCTCCAACTTTT | 55632 |
rs796108887 | snp | C/G | | | upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30558543 | TGAGCCCTTATCTGA[C/G]GGGGGAAATAAAATT | 55632 |
rs796203800 | in-del | -/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30586080 | ATATTTGTTTCAAAT[-/G]TTTTTTGACAAACAG | 55632 |
rs796218584 | in-del | -/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30593252 | TTCTGAAATTCTGTA[-/T]TAAGTAAGTCTCACT | 55632 |
rs796311144 | in-del | -/TG | | | intron-variant | G2E3 | GRCh38.p7 | 14:30595850 | GAAGAGACTAGAGAT[-/TG]TGCTATCAAAGAAAC | 55632 |
rs796369459 | in-del | -/GTGTGTGTGTGTGTGTGTGT | | | intron-variant | G2E3 | GRCh38.p7 | 14:30596136 | GGTGGGTGGGTGTGC[-/GTGTGTGTGTGTGTGTGTGT]GTGTGTGTGTCACTT | 55632 |
rs796496983 | snp | A/G | | | intron-variant, upstream-variant-2KB | G2E3 | GRCh38.p7 | 14:30577239 | AAAAAAAAAAAAAAA[A/G]AAAAGAAAAAGAAAA | 55632 |
rs796507974 | snp | G/T | | | intron-variant | G2E3 | GRCh38.p7 | 14:30579765 | GACCTTGGACAGGTG[G/T]TTAACCTTTCTGAGA | 55632 |
rs796648530 | in-del | -/GT | | | intron-variant | G2E3 | GRCh38.p7 | 14:30596164 | TGTGTGTGTGTGTGT[-/GT]CACTTGCTAATTGTC | 55632 |
rs796654043 | snp | A/G | | | intron-variant | G2E3 | GRCh38.p7 | 14:30579822 | TTATATTTACCTAGT[A/G]GCATTATTATGTTTT | 55632 |
rs796659116 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | G2E3 | GRCh38.p7 | 14:30618856 | AACCAGTGCATAATT[A/C]TTACATTAGATTTTA | 55632 |
rs797001084 | multinucleotide-polymorphism | CGT/TGC | | | intron-variant | G2E3 | GRCh38.p7 | 14:30573430 | TGTGTGTGTGTGTGT[CGT/TGC]TGTGTGTGTGTCTCT | 55632 |