SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs754498 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | SCAP | GRCh38.p7 | 3:47416098 | CCTTGGGGAGGGGGC[A/G]TCCCTTGCCCTTAGT | 22937 |
rs878659 | snp | C/T | 0.496681 | 0.0405994 | intron-variant | SCAP | GRCh38.p7 | 3:47459172 | GTCCATGGGCCAAGA[C/T]ATTGTGTGAAATGAC | 22937 |
rs881264 | snp | A/T | 0 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47458608 | TTGAAGTAAGACCAA[A/T]TTATATTAGTTGGTT | 22937 |
rs900690 | snp | C/T | 0.0263046 | 0.111626 | synonymous-codon | SCAP | GRCh38.p7 | 3:47420710 | GTAGCGCGTTGGCTG[C/T]CCCACTGGCTTGGCT | 22937 |
rs900691 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | SCAP | GRCh38.p7 | 3:47421097 | CCCAAGAGGAGCAGT[A/G]CCCGGACTGCAGCCA | 22937 |
rs900692 | snp | C/G | 0.0883596 | 0.190715 | intron-variant | SCAP | GRCh38.p7 | 3:47442636 | CATTATTTTGAGATA[C/G]AGTACCAGTGATATG | 22937 |
rs1038394 | snp | A/G | 0.496681 | 0.0405994 | intron-variant | SCAP | GRCh38.p7 | 3:47422632 | TGGCAGAGGCATGGC[A/G]AGGCCCCCCAGCCCT | 22937 |
rs1051496 | snp | C/T | 0 | 0 | utr-variant-3-prime, downstream-variant-500B | PTPN23, SCAP | GRCh38.p7 | 3:47413355 | AATGTACTGCAGGCT[C/T]TGGGTCAGGTTCTGC | 22937 |
rs1078224 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SCAP | GRCh38.p7 | 3:47415386 | agtttcttcatccgt[A/G]aaatggggataagag | 22937 |
rs1872165 | snp | C/T | 0.0854556 | 0.188216 | intron-variant | SCAP | GRCh38.p7 | 3:47423267 | ACCCCAGATCCCCAG[C/T]TTCTACCAGCAGGGC | 22937 |
rs2046376 | snp | C/T | 1.64732e-05 | 0.0028699 | intron-variant, stop-gained, upstream-variant-2KB, utr-variant-5-prime | SCAP | GRCh38.p7 | 3:47427544 | TTCCCAGTCATTCTG[C/T]CAGAAGTTCCCAGGG | 22937 |
rs2101247 | snp | A/G | 0.48155 | 0.0942576 | intron-variant | SCAP | GRCh38.p7 | 3:47452813 | AGCAGGGCAGGCATC[A/G]TAGCTAACTAATGTC | 22937 |
rs2306628 | snp | C/T | 0.0562768 | 0.158035 | intron-variant | SCAP | GRCh38.p7 | 3:47417260 | AAGGCCCACAATCCC[C/T]GGGGCGGACAGCCGC | 22937 |
rs3077503 | in-del | -/TTTTTTTTT | | | intron-variant | SCAP | GRCh38.p7 | 3:47416636 | ttttttttttttttt[-/TTTTTTTTT]gagacggagtctcgc | 22937 |
rs3077506 | in-del | -/TG | | | intron-variant, frameshift-variant, upstream-variant-2KB, utr-variant-5-prime | SCAP | GRCh38.p7 | 3:47427542 | CGTTCCCAGTCATTC[-/TG]CCAGAAGTTCCCAGG | 22937 |
rs3796354 | snp | A/G | | | intron-variant | SCAP | GRCh38.p7 | 3:47416208 | CAGGTGCCTTCTGCC[A/G]GACGCCTTTGCCTGC | 22937 |
rs3830277 | in-del | -/GCCAC | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | PTPN23, SCAP | GRCh38.p7 | 3:47413809 | CAGTGCATTGGCCCC[-/GCCAC]CACACAGCACCCCAG | 22937 |
rs3898288 | snp | G/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47467066 | tccctaattcaccca[G/T]ggtggagtgcattgc | 22937 |
rs4547726 | snp | C/T | 0 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47419108 | CACAGGTGGGTGGGT[C/T]TCATTCTGGTGAGGG | 22937 |
rs4599333 | snp | C/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47442828 | AGAAAACCTACTGTC[C/T]TAAGACACTGGCCCA | 22937 |
rs4858811 | snp | C/G | 0.481627 | 0.0940692 | intron-variant | SCAP | GRCh38.p7 | 3:47439034 | ctattctaagcactt[C/G]atatgtacagataca | 22937 |
rs4858812 | snp | C/T | 0.0854556 | 0.188216 | intron-variant | SCAP | GRCh38.p7 | 3:47439036 | attctaagcacttga[C/T]atgtacagatacatc | 22937 |
rs4858816 | snp | A/G | 0.5 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47462771 | AAAAAAAAAAAAAAA[A/G]AAAGAAAGAAAGAAA | 22937 |
rs4858868 | snp | A/G | 0.496649 | 0.0407971 | downstream-variant-500B | PTPN23, SCAP | GRCh38.p7 | 3:47413596 | TTGCTCATCCTCCCC[A/G]TGCCACACTGTATGT | 22937 |
rs4858889 | snp | A/G | 0.107341 | 0.205301 | intron-variant | SCAP | GRCh38.p7 | 3:47438867 | AGCGTTTGCATAGTA[A/G]TCACAGAGTATAGTC | 22937 |
rs4858893 | snp | C/T | 0.496984 | 0.0387176 | intron-variant | SCAP | GRCh38.p7 | 3:47443307 | TCTCTCTCTCTCTCT[C/T]TCTCCCTCCCCGCCC | 22937 |
rs4858894 | snp | C/G | 0.508232 | 0.061893 | intron-variant | SCAP | GRCh38.p7 | 3:47443463 | GGCATTCTTCCCCCC[C/G]CTCCTCTATGCACAA | 22937 |
rs4858896 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | SCAP | GRCh38.p7 | 3:47455364 | acttgggaggccgag[A/G]tgggcagatcacctg | 22937 |
rs5848833 | in-del | -/GC | | | intron-variant, frameshift-variant, upstream-variant-2KB, utr-variant-5-prime | SCAP | GRCh38.p7 | 3:47427543 | GTTCCCAGTCATTCT[-/GC]CAGAAGTTCCCAGGG | 22937 |
rs5848834 | in-del | -/A | 0 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47452927 | AGATCCTGTCTCTAC[-/A]AAAAAAAAAAAAATT | 22937 |
rs6442066 | snp | C/T | 0.039522 | 0.134904 | intron-variant | SCAP | GRCh38.p7 | 3:47414735 | GCCCTCTGTTCTTCA[C/T]CAGGACTCTTCCAGC | 22937 |
rs6442068 | snp | C/T | 0.0854556 | 0.188216 | intron-variant | SCAP | GRCh38.p7 | 3:47433259 | CTTTATCAAGGACAG[C/T]CAATGGAGGTGAGAT | 22937 |
rs6442069 | snp | A/G | 0.0854556 | 0.188216 | intron-variant | SCAP | GRCh38.p7 | 3:47462343 | AGCCTCTGCCCCATC[A/G]GCTATACAACCTCTG | 22937 |
rs6765597 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SCAP | GRCh38.p7 | 3:47463902 | ggatacagttgtaca[A/G]tcgtggctcactgcg | 22937 |
rs6772227 | snp | C/T | 0.5 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47435469 | TATATAATATAAACA[C/T]ACACACACACACACA | 22937 |
rs6772923 | snp | A/G | 0 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47473455 | GGAGCTCAGGTGGCA[A/G]AGGTGTGGCAGACCT | 22937 |
rs6785538 | snp | C/T | 0.0858192 | 0.188533 | intron-variant | SCAP | GRCh38.p7 | 3:47444857 | gctcaatgaaatctc[C/T]gtctcctgggtttaa | 22937 |
rs6788191 | snp | C/T | 0.00563631 | 0.0527863 | intron-variant | SCAP | GRCh38.p7 | 3:47415068 | CCGTCCCACCAAGTG[C/T]GAACACCTGCCCACC | 22937 |
rs6792461 | snp | C/T | 0.481473 | 0.0944461 | intron-variant | SCAP | GRCh38.p7 | 3:47431678 | ggagaggaagatcag[C/T]ggtaaaatgtcctcc | 22937 |
rs6792488 | snp | C/T | 0.481396 | 0.0946345 | intron-variant | SCAP | GRCh38.p7 | 3:47461859 | AGCAACACGGTGAAA[C/T]CCTATCTCTACTAAA | 22937 |
rs6800271 | snp | A/T | 0.495056 | 0.049474 | intron-variant | SCAP | GRCh38.p7 | 3:47429297 | ataacaCATCTACTA[A/T]GGGCAAAGCACTGTG | 22937 |
rs6800588 | snp | C/T | 0.222333 | 0.248464 | intron-variant | SCAP | GRCh38.p7 | 3:47459763 | tcagctgtgcacgta[C/T]tgtcttgataaacat | 22937 |
rs6800839 | snp | A/G | | | intron-variant | SCAP | GRCh38.p7 | 3:47416745 | cattctcctgcctca[A/G]cctcccaagtagctg | 22937 |
rs6801270 | snp | A/G | 0.0854556 | 0.188216 | intron-variant | SCAP | GRCh38.p7 | 3:47460576 | ttgtctttttgagac[A/G]gagtctcactctgtc | 22937 |
rs6804017 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | SCAP | GRCh38.p7 | 3:47430743 | GGAGACAAGGAAACA[C/T]GGCCCTAGACAGCGG | 22937 |
rs7372780 | snp | C/G | 0.0861826 | 0.188849 | intron-variant | SCAP | GRCh38.p7 | 3:47421795 | TGGGGGAAAGACGGG[C/G]GAGAAAAGATGGCAT | 22937 |
rs7611273 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SCAP | GRCh38.p7 | 3:47467327 | gaagatatacaggct[C/T]ggtggggtggctcat | 22937 |
rs7615610 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | SCAP | GRCh38.p7 | 3:47449222 | gttctgaggaacagc[A/C]caagagttcatatgc | 22937 |
rs7619813 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant | SCAP | GRCh38.p7 | 3:47445405 | gtgcccgccactacg[C/G]ccagctattttttcg | 22937 |
rs7621853 | snp | C/T | 0.0894459 | 0.191631 | intron-variant | SCAP | GRCh38.p7 | 3:47451201 | tatcacagaaaagca[C/T]acaaattataagcac | 22937 |
rs7644043 | snp | C/T | 0.0854556 | 0.188216 | intron-variant | SCAP | GRCh38.p7 | 3:47429079 | tcacccttccttcca[C/T]caatcatctgctaat | 22937 |
rs7648696 | snp | C/T | 0.450985 | 0.148678 | intron-variant | SCAP | GRCh38.p7 | 3:47440732 | aaaattagtggtgca[C/T]gcctatagtcccaac | 22937 |
rs7649234 | snp | C/G | 0.495095 | 0.0492773 | intron-variant | SCAP | GRCh38.p7 | 3:47452890 | GCCAGGAAAGTTCAA[C/G]ACCAGCCTGGGCAAC | 22937 |
rs7651762 | snp | A/G | 0.481473 | 0.0944461 | intron-variant | SCAP | GRCh38.p7 | 3:47428994 | atactaactcccccc[A/G]gaatttgcacatggg | 22937 |
rs9683033 | snp | C/T | 0.496746 | 0.040204 | intron-variant | SCAP | GRCh38.p7 | 3:47448330 | actgtcctgaaatca[C/T]ttattagtgccagag | 22937 |
rs9683177 | snp | A/G | 0.496714 | 0.0404017 | intron-variant | SCAP | GRCh38.p7 | 3:47449003 | aatcaacctaattag[A/G]tccagtccacaagtt | 22937 |
rs9818988 | snp | A/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47445646 | gcgcgatctcagctc[A/T]ctgtaaactccgcct | 22937 |
rs9823177 | snp | C/T | | | synonymous-codon | SCAP | GRCh38.p7 | 3:47418169 | TAGGCAATCCCCGGT[C/T]TGCGCGTCCCACACG | 22937 |
rs9825749 | snp | A/G | 0 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47471600 | ggtctcgaactcctg[A/G]cctcaggtgatccac | 22937 |
rs9836061 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SCAP | GRCh38.p7 | 3:47466135 | agactgtcttaaaaa[A/C]caaaaaaaaaaaaaa | 22937 |
rs9840942 | snp | A/T | 0 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47433570 | GTGCTAACATTGCAT[A/T]AAAAGGTTAATGAAG | 22937 |
rs9843160 | snp | A/G | 0 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47462066 | CATTCAGATTTAAAT[A/G]TTTACTATAATCAGT | 22937 |
rs9867128 | snp | A/G | 0 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47447224 | ggctaacacagtgaa[A/G]ccccttctctactaa | 22937 |
rs9867204 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SCAP | GRCh38.p7 | 3:47447464 | tgaggcaaaggtggg[C/T]ggattacaaggtcag | 22937 |
rs9872793 | snp | C/T | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | SCAP, LOC105377073 | GRCh38.p7 | 3:47478727 | gtgggatccacccgc[C/T]tcagcctctcaaagt | 22937 |
rs9884092 | snp | G/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47441901 | tttttttttttttgg[G/T]cttgctatgttgccc | 22937 |
rs10446461 | snp | G/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47444890 | tattctcctgactca[G/T]cctcccaagtagctg | 22937 |
rs10652619 | in-del | -/AGAATG | 0 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47438430 | AGAAACGACTACAAG[-/AGAATG]TGATCAGAATTCATT | 22937 |
rs10712274 | in-del | -/T | 0.357664 | 0.225629 | intron-variant | SCAP | GRCh38.p7 | 3:47451415 | TTTTTTTTTTTTTTT[-/T]GAGACAGGGTCTCAC | 22937 |
rs10865947 | snp | A/G | 0.0861826 | 0.188849 | intron-variant | SCAP | GRCh38.p7 | 3:47424671 | AGGGAGGGCCCTGTG[A/G]AGGGTATGGCAGACG | 22937 |
rs11130128 | snp | C/T | 0.481319 | 0.0948228 | intron-variant | SCAP | GRCh38.p7 | 3:47445142 | ttgtccattcatcag[C/T]tgataaacatttggg | 22937 |
rs11130129 | snp | C/G | 0.480539 | 0.0967035 | intron-variant | SCAP | GRCh38.p7 | 3:47448395 | ggaaatttctacgta[C/G]acttatcatgttatc | 22937 |
rs11308011 | in-del | -/A | | | intron-variant | SCAP | GRCh38.p7 | 3:47432315 | CAAGACTCCGTCTTG[-/A]AAAAAAAAAAAAAAA | 22937 |
rs11386934 | in-del | -/A | 0.145642 | 0.227177 | intron-variant | SCAP | GRCh38.p7 | 3:47453397 | AAAAATTTTTAATGG[-/A]AAAAAAAAAAGACCT | 22937 |
rs11546518 | snp | A/G/T | 3.39207e-05 | 0.00411816 | missense | SCAP | GRCh38.p7 | 3:47418359 | TATGCGCCACCCGAG[A/G/T]CGGAGATCGTGCCGC | 22937 |
rs11707272 | snp | C/T | 0.0854556 | 0.188216 | upstream-variant-2KB, intron-variant | SCAP, LOC105377073 | GRCh38.p7 | 3:47478116 | TCAGGAGCCTGTCTT[C/T]TAACCACCTCCATGG | 22937 |
rs11707638 | snp | A/C | | | intron-variant | SCAP | GRCh38.p7 | 3:47452288 | cggctactcaggaga[A/C]tgaggtgggacaatc | 22937 |
rs11708770 | snp | A/T | 0.481473 | 0.0944461 | upstream-variant-2KB, intron-variant, nc-transcript-variant | SCAP, LOC105377073 | GRCh38.p7 | 3:47476284 | CTTGGGCAACGTAGG[A/T]GACCTCCGTCTCCAC | 22937 |
rs11709190 | snp | A/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47455094 | atatatatatatata[A/T]aatcaactgaaaacc | 22937 |
rs11711824 | snp | C/T | 0.496778 | 0.0400063 | intron-variant, upstream-variant-2KB | SCAP | GRCh38.p7 | 3:47426771 | GAGGCCTAGGAGAGC[C/T]GATCAGAAGCACCTC | 22937 |
rs11712403 | snp | A/T | 0 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47463895 | ccaggctggatacag[A/T]tgtacaatcgtggct | 22937 |
rs11712590 | snp | A/G | 0.403334 | 0.197456 | intron-variant | SCAP | GRCh38.p7 | 3:47437340 | gctactcagaaggct[A/G]aggcaggaaaatcac | 22937 |
rs11713842 | snp | A/G | | | intron-variant | SCAP | GRCh38.p7 | 3:47438729 | tgaggcaggagaatc[A/G]cttgaacccgggagg | 22937 |
rs11716661 | snp | G/T | 0.481396 | 0.0946345 | upstream-variant-2KB, intron-variant, nc-transcript-variant | SCAP, LOC105377073 | GRCh38.p7 | 3:47476283 | ACTTGGGCAACGTAG[G/T]AGACCTCCGTCTCCA | 22937 |
rs11716763 | snp | C/T | 0.480853 | 0.0959518 | upstream-variant-2KB, intron-variant | SCAP, LOC105377073 | GRCh38.p7 | 3:47476776 | AAACACAGGTCCCCA[C/T]CTGCCCAGCTCTGGC | 22937 |
rs11717442 | snp | C/T | 0.277778 | 0.248452 | intron-variant | SCAP | GRCh38.p7 | 3:47443306 | CTCTCTCTCTCTCTC[C/T]CTCTCCCTCCCCGCC | 22937 |
rs11718842 | snp | A/C | 0 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47420806 | TCAGGGCCTGAGTCC[A/C]CCATCCAGAGGCTGC | 22937 |
rs11721160 | snp | A/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47443276 | CACACACACACACAC[A/T]CTCTCTCTCTCTCTC | 22937 |
rs11917409 | snp | A/C | | | intron-variant | SCAP | GRCh38.p7 | 3:47446370 | tagagacgaagtttc[A/C]ctatgttggccaggc | 22937 |
rs12054363 | snp | A/G | 0 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47448144 | ttttccatctactta[A/G]atctttgatttcttt | 22937 |
rs12054364 | snp | A/G | | | intron-variant | SCAP | GRCh38.p7 | 3:47448209 | gtacatgttttgtta[A/G]atttatacctaccat | 22937 |
rs12487736 | snp | C/T | 0.4665 | 0.125011 | missense | SCAP | GRCh38.p7 | 3:47418189 | CGTCCCACACGCAGA[C/T]GTGGCCTGCCAGGCA | 22937 |
rs12490383 | snp | C/T | 0.3512 | 0.228601 | intron-variant | SCAP | GRCh38.p7 | 3:47452667 | GCCCAGAAATCTCTA[C/T]TTAACACACCCTCCA | 22937 |
rs12491029 | snp | A/G | 0.0883596 | 0.190715 | intron-variant | SCAP | GRCh38.p7 | 3:47467605 | aagaccccgtctcaa[A/G]aaaaagaaaaagaaa | 22937 |
rs12492433 | snp | A/G | 0.497502 | 0.035255 | intron-variant | SCAP | GRCh38.p7 | 3:47474067 | TCAGGAGATAGAGAC[A/G]ATCCTGGCTAACACG | 22937 |
rs12631697 | snp | A/G | 0.226484 | 0.248892 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | SCAP, LOC105377073 | GRCh38.p7 | 3:47477000 | TTCTCTGGGAGTTCC[A/G]GAAAGTGCAGATCTA | 22937 |
rs12632132 | snp | C/T | 0.496842 | 0.0396107 | intron-variant | SCAP | GRCh38.p7 | 3:47435529 | ACACAGATAGATAGG[C/T]GCCTGCCACTACATC | 22937 |
rs12636851 | snp | C/T | 0.481627 | 0.0940692 | intron-variant | SCAP | GRCh38.p7 | 3:47422077 | CTTCTCCCTCAAAAA[C/T]GGGAAACAGGTGTGA | 22937 |
rs13058785 | snp | C/G | 0 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47443631 | ACGCTAAAAAGCTTA[C/G]GTCTCTGACATAATG | 22937 |
rs13060272 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SCAP | GRCh38.p7 | 3:47438674 | caaaaattggccgga[C/T]gcggtggcacacgcc | 22937 |
rs13061438 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SCAP | GRCh38.p7 | 3:47447101 | aattgcttggcatct[C/T]tgtcaaaaagcagtt | 22937 |
rs13062919 | snp | C/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47441940 | CCTGAACTCCTGGCC[C/T]CAAGTGATTCTCTCA | 22937 |
rs13063125 | snp | A/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47442041 | TAATCAGGGAAGAGC[A/T]TGAGATCATTAGCAA | 22937 |
rs13063127 | snp | G/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47442047 | GGGAAGAGCTTGAGA[G/T]CATTAGCAACTGAAC | 22937 |
rs13070333 | snp | A/C | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | SCAP, LOC105377073 | GRCh38.p7 | 3:47475816 | GTGGTGGCAGCACCT[A/C]CCAAGCTgcggcggc | 22937 |
rs13078254 | snp | A/T | 0 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47441812 | ACTGGACCACTTCCT[A/T]ATGTTATACCTGAAG | 22937 |
rs13078883 | snp | G/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47441899 | ttttttttttttttt[G/T]gtcttgctatgttgc | 22937 |
rs13082775 | snp | A/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47441923 | atgttgcccaggctg[A/T]tcctgaactcctggc | 22937 |
rs13082967 | snp | A/C | | | intron-variant | SCAP | GRCh38.p7 | 3:47442052 | GAGCTTGAGATCATT[A/C]GCAACTGAACTGAAC | 22937 |
rs13082972 | snp | A/C | 0 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47442061 | ATCATTAGCAACTGA[A/C]CTGAACAGGGAGTTC | 22937 |
rs13083401 | snp | G/T | 0 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47442064 | ATTAGCAACTGAACT[G/T]AACAGGGAGTTCCCT | 22937 |
rs13087188 | snp | A/C | | | intron-variant | SCAP | GRCh38.p7 | 3:47448033 | aaaaaaaaaaaaaaa[A/C]CTTGAtagaattttg | 22937 |
rs13100413 | snp | C/T | 0.0854556 | 0.188216 | intron-variant | SCAP | GRCh38.p7 | 3:47464235 | tagtcaggctggtct[C/T]gaactcctgatctca | 22937 |
rs13101111 | snp | G/T | 0 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47443531 | GAAACCCTTTACATA[G/T]GGATGGCCTCCTCAA | 22937 |
rs13101207 | snp | A/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47441888 | TCTTTTTTTTttttt[A/T]ttttttttttggtct | 22937 |
rs13101219 | snp | G/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47441911 | tttggtcttgctatg[G/T]tgcccaggctgatcc | 22937 |
rs13101220 | snp | G/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47441912 | ttggtcttgctatgt[G/T]gcccaggctgatcct | 22937 |
rs17079634 | snp | C/T | 0.0741063 | 0.177655 | intron-variant | SCAP | GRCh38.p7 | 3:47432634 | ATGCCTGCAATGTAC[C/T]GTCTACTGCCCGAGT | 22937 |
rs17079656 | snp | A/G | 0.0693013 | 0.172766 | intron-variant | SCAP | GRCh38.p7 | 3:47463359 | CCTCATTCCATCCTC[A/G]ATAAATCTTTCTAAA | 22937 |
rs17080872 | snp | C/T | 0.353803 | 0.227431 | intron-variant | SCAP | GRCh38.p7 | 3:47443539 | TTACATAGGGATGGC[C/T]TCCTCAAAACACACT | 22937 |
rs17784714 | snp | C/T | 0.128288 | 0.218372 | intron-variant | SCAP | GRCh38.p7 | 3:47470208 | CCATTACCAGTCTTA[C/T]TGCTGATGCTGGCAA | 22937 |
rs17849129 | snp | A/G | 0.0181185 | 0.0934397 | missense | SCAP | GRCh38.p7 | 3:47417560 | TCTGTGGCCGCTCTC[A/G]GGACTCCCCAGGCTA | 22937 |
rs17849130 | snp | C/T | 0.000313676 | 0.0125196 | missense | SCAP | GRCh38.p7 | 3:47417497 | AGGAGGAGGGGCTGG[C/T]GGCCGTCTGCACACC | 22937 |
rs17849132 | snp | A/G | 0.0105259 | 0.0717786 | intron-variant | SCAP | GRCh38.p7 | 3:47415199 | GGAGAGGCCCCTGGC[A/G]GCTGTTCTTCTCTTC | 22937 |
rs17849133 | snp | C/T | 1.658e-05 | 0.00287919 | synonymous-codon | SCAP | GRCh38.p7 | 3:47414097 | TCCTTGCCTCCAGGA[C/T]CTGGGCTGTGGTGCA | 22937 |
rs28489877 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SCAP | GRCh38.p7 | 3:47450647 | CCTGCCTATAGGCAC[A/G]TACCACCATGAGAGA | 22937 |
rs28580090 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | SCAP | GRCh38.p7 | 3:47428182 | TAGAGCTTGCTTCTC[A/G]TCGGCAGAGACACCA | 22937 |
rs28653422 | snp | A/C | | | intron-variant | SCAP | GRCh38.p7 | 3:47443574 | TACAAATAGTGATTC[A/C]CTCGTGAAGAAGGTC | 22937 |
rs28671733 | snp | A/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47452940 | ACAAAAAAAAAAAAA[A/T]TTTAAATTAGCCAAT | 22937 |
rs28694581 | snp | A/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47456885 | ATTTTGACAAAATCA[A/T]TTTAAAAATACCAAA | 22937 |
rs34222894 | in-del | -/C | | | intron-variant | SCAP | GRCh38.p7 | 3:47442865 | CAAGGCAACCCAAAA[-/C]ACATACCAGCAGGCT | 22937 |
rs34363569 | in-del | -/AAA/AAT/T | 0.0995161 | 0.199636 | intron-variant | SCAP | GRCh38.p7 | 3:47472460 | AATAATAATAATAAT[-/AAA/AAT/T]TAAATGAAGCTGAAA | 22937 |
rs34472664 | in-del | -/AAAA/AAAAAA | 0.0962929 | 0.197165 | intron-variant | SCAP | GRCh38.p7 | 3:47473080 | GCGAAACTCCATCTC[-/AAAA/AAAAAA]AAAAAAAAAAAAAAA | 22937 |
rs34486358 | in-del | -/C | | | intron-variant | SCAP | GRCh38.p7 | 3:47430367 | CACATATGCAACCCT[-/C]CAGTAACAGGCATGT | 22937 |
rs34559057 | in-del | -/G | | | intron-variant | SCAP | GRCh38.p7 | 3:47437256 | CCAGCCTGACCAACA[-/G]GGGAGAAACCCTGTC | 22937 |
rs34683292 | in-del | -/A | 0.481087 | 0.0953875 | intron-variant, upstream-variant-2KB | SCAP, LOC105377073 | GRCh38.p7 | 3:47474264 | GCGAGACTCCATCTC[-/A]AAAAAAAAAAAGAAA | 22937 |
rs34721584 | in-del | -/A | | | intron-variant | SCAP | GRCh38.p7 | 3:47472919 | AACCTCGCCTCTACT[-/A]AAAATACAAAATTAG | 22937 |
rs34729126 | in-del | -/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47455092 | ATATATATATATATA[-/T]ATAATCAACTGAAAA | 22937 |
rs34742333 | in-del | -/C | | | frameshift-variant | SCAP | GRCh38.p7 | 3:47417548 | CAGCTGAAGTCATAG[-/C]CTGGGGAGTCCCGAG | 22937 |
rs34798139 | in-del | -/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47443304 | CTCTCTCTCTCTCTC[-/T]CTCTCTCCCTCCCCG | 22937 |
rs34834510 | in-del | -/C | | | frameshift-variant, intron-variant, upstream-variant-2KB | SCAP | GRCh38.p7 | 3:47425609 | GACCATGTCGATCTT[-/C]CCCTGGAGGGCAGAG | 22937 |
rs34931190 | snp | A/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47443272 | CACACACACACACAC[A/T]CTCTCTCTCTCTCTC | 22937 |
rs34950272 | snp | C/T | 0.00179054 | 0.0298674 | synonymous-codon | SCAP | GRCh38.p7 | 3:47414599 | CACGGTCGTGATGGC[C/T]CCTGAGTGGCCCTGA | 22937 |
rs35005516 | in-del | -/A | | | intron-variant | SCAP | GRCh38.p7 | 3:47424967 | AAGTAAACATCAGTG[-/A]AAAAGGCGACAAATT | 22937 |
rs35011639 | in-del | -/A/AA | | | intron-variant | SCAP | GRCh38.p7 | 3:47437422 | GTGAAACTCAATCTC[-/A/AA]AAAAAAAAAAAAAAA | 22937 |
rs35026171 | in-del | -/G | | | intron-variant | SCAP | GRCh38.p7 | 3:47451798 | GAGCTGGATACCCTT[-/G]CTGCACTTAGAACAA | 22937 |
rs35032933 | snp | A/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47443270 | CACACACACACACAC[A/T]CACACACTCTCTCTC | 22937 |
rs35075035 | in-del | -/A | | | intron-variant | SCAP | GRCh38.p7 | 3:47448003 | GGGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 22937 |
rs35232550 | in-del | -/C | | | upstream-variant-2KB, intron-variant | SCAP, LOC105377073 | GRCh38.p7 | 3:47476594 | CCATTTTCCACAGGG[-/C]AACAGGTATTTGTTA | 22937 |
rs35491591 | in-del | -/C | | | intron-variant | SCAP | GRCh38.p7 | 3:47427676 | CCAGAGCTGCACAGG[-/C]AGACAGGACAAGGCA | 22937 |
rs35503021 | in-del | -/G | | | intron-variant | SCAP | GRCh38.p7 | 3:47450484 | GTAGTGGTTGCTTGT[-/G]CTTTGTGTAATGTGA | 22937 |
rs35628908 | snp | C/T | 0.00560517 | 0.0526419 | synonymous-codon | SCAP | GRCh38.p7 | 3:47414240 | GCTGATGAGGTCATC[C/T]AGGCCACTGCTGATG | 22937 |
rs35707640 | snp | C/T | 0.00138304 | 0.0262604 | synonymous-codon | SCAP | GRCh38.p7 | 3:47417154 | CAGAGCGGTAATGCC[C/T]GAGGAGACCTCCTCG | 22937 |
rs35796019 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SCAP | GRCh38.p7 | 3:47451988 | CTCTATTCCCTCTTC[C/T]CTTTATAGGCTGGTT | 22937 |
rs35827617 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | SCAP | GRCh38.p7 | 3:47451940 | GTGCCAACCTCATTC[A/C]CATCTCAGGGGCCTG | 22937 |
rs35903310 | snp | A/C | 0 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47455590 | ACAGAGCAAGACTCC[A/C]CCTCAAAAAAAAAAA | 22937 |
rs35915520 | snp | C/T | 0.000478528 | 0.0154608 | synonymous-codon | SCAP | GRCh38.p7 | 3:47419489 | AGGTGACTCGCCTGG[C/T]GACGTCTGGTTCTCA | 22937 |
rs35996993 | in-del | -/T | 0.5 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47445894 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTTGC | 22937 |
rs36012077 | in-del | -/C | | | upstream-variant-2KB, intron-variant | SCAP, LOC105377073 | GRCh38.p7 | 3:47477605 | AAAGAAAGAAAGAAT[-/C]TTTTTAGGTTATTTT | 22937 |
rs36032244 | snp | A/C | | | intron-variant | SCAP | GRCh38.p7 | 3:47442136 | CTATAAATGTTTTAG[A/C]CAATGAATCTGAAGA | 22937 |
rs45453398 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant, utr-variant-3-prime, downstream-variant-500B | PTPN23, SCAP | GRCh38.p7 | 3:47413771 | GGCTGGAAGATACTC[A/G]GCTCTTTCCCCCAAG | 22937 |
rs55648522 | snp | A/G | | | intron-variant | SCAP | GRCh38.p7 | 3:47427903 | GCCCATCAGCTCTGA[A/G]GACGGGCAAGTGTAC | 22937 |
rs55666921 | snp | A/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47443274 | CACACACACACACAC[A/T]CACTCTCTCTCTCTC | 22937 |
rs55742438 | snp | A/G | | | intron-variant | SCAP | GRCh38.p7 | 3:47473122 | TGGAAGCAGGTACAA[A/G]AACAGCATAAAAGGA | 22937 |
rs55797252 | in-del | -/G | | | intron-variant | SCAP | GRCh38.p7 | 3:47430263 | GGACTCAAACCAAGG[-/G]TCTCCTCACTAAATA | 22937 |
rs55799205 | snp | A/G | | | intron-variant | SCAP | GRCh38.p7 | 3:47473357 | GCTCGATATCACCCA[A/G]AATTATTACTCTGAG | 22937 |
rs55946521 | in-del | -/TACACACA | | | intron-variant | SCAP | GRCh38.p7 | 3:47435469 | TATATAATATAAACA[-/TACACACA]CACACACACACACAC | 22937 |
rs56132307 | in-del | -/AAA | 0 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47448031 | AAAAAAAAAAAAAAA[-/AAA]CTTGATAGAATTTTG | 22937 |
rs56260584 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | SCAP | GRCh38.p7 | 3:47442765 | GAGCCCAAGCTCCCA[C/T]TGTGTAAAAAGCATA | 22937 |
rs56318050 | snp | A/G | | | intron-variant | SCAP | GRCh38.p7 | 3:47471606 | GAACTCCTGACCTCA[A/G]GTGATCCACCCTCCT | 22937 |
rs56390704 | snp | A/G | | | intron-variant | SCAP | GRCh38.p7 | 3:47473466 | GGCAGAGGTGTGGCA[A/G]ACCTGGTTTGAAGGA | 22937 |
rs56393696 | snp | A/G | | | intron-variant | SCAP | GRCh38.p7 | 3:47471591 | GGTCAGGCTGGTCTC[A/G]AACTCCTGACCTCAG | 22937 |
rs56398518 | snp | C/T | 0.138546 | 0.223781 | intron-variant | SCAP | GRCh38.p7 | 3:47458962 | AGGTATGTGCCACCA[C/T]GCCTGGCTAATTTTT | 22937 |
rs57136596 | in-del | -/TG | | | intron-variant | SCAP | GRCh38.p7 | 3:47419138 | GCTGGCAGCCACCAG[-/TG]ACTCCTCAGAGCAAC | 22937 |
rs57304464 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SCAP | GRCh38.p7 | 3:47455759 | CATCTAGAAATGTAA[C/T]AGTCCCAATAAAAAC | 22937 |
rs57702290 | in-del | -/CA | | | intron-variant | SCAP | GRCh38.p7 | 3:47435518 | ACACACACACACACA[-/CA]GATAGATAGGCGCCT | 22937 |
rs57815378 | snp | A/C | 0.0547245 | 0.156101 | intron-variant | SCAP | GRCh38.p7 | 3:47419140 | TGGCAGCCACCAGTG[A/C]CTCCTCAGAGCAACC | 22937 |
rs57892253 | in-del | -/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47469103 | TGCAATCCCAGCACT[-/T]TGGGGATGCCAAGGT | 22937 |
rs57940072 | in-del | -/TTTCA | | | intron-variant | SCAP | GRCh38.p7 | 3:47448729 | CTGATTTTCTGTTCA[-/TTTCA]AGAGCATTCACCCTT | 22937 |
rs58162151 | in-del | -/AA | | | intron-variant | SCAP | GRCh38.p7 | 3:47438834 | AAAAAAAAAAAAAAA[-/AA]TTTTAGGCTGTGGCT | 22937 |
rs58248669 | snp | A/G | | | intron-variant | SCAP | GRCh38.p7 | 3:47447699 | GACTCAAAAAAAAAA[A/G]GAAAAGAAAAGAAAA | 22937 |
rs58460988 | in-del | -/TATATA | | | intron-variant | SCAP | GRCh38.p7 | 3:47455090 | ATATATATATATATA[-/TATATA]ATCAACTGAAAACCT | 22937 |
rs58488052 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SCAP | GRCh38.p7 | 3:47466154 | AAAAAAAAAAAAAAA[A/G]AAAGAAAGAAATTCT | 22937 |
rs59527052 | snp | A/G | | | intron-variant | SCAP | GRCh38.p7 | 3:47448490 | CTCCTCTCTTTTTGA[A/G]ACTTCAAAAACATAA | 22937 |
rs59586735 | snp | C/T | 0.481932 | 0.0933148 | upstream-variant-2KB, intron-variant | SCAP, LOC105377073 | GRCh38.p7 | 3:47476835 | TGGGGGGACTTTGAT[C/T]ATGCTACTGCATGCC | 22937 |
rs59605203 | in-del | -/AAAA/AAAAA | 0 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47473099 | AAAAAAAAAAAAAAA[-/AAAA/AAAAA]CAGACTGTGGAAGCA | 22937 |
rs59825859 | snp | C/T | 0.128976 | 0.218754 | intron-variant | SCAP | GRCh38.p7 | 3:47470600 | GGGCGCAGTGGCTCA[C/T]GCCTATAATCCCAAC | 22937 |
rs59995300 | snp | A/G | | | intron-variant | SCAP | GRCh38.p7 | 3:47447704 | AAAAAAAAAAAGAAA[A/G]GAAAAGAAAAAAGAA | 22937 |
rs60178960 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47424813 | CTGATGGGCCAAAGT[C/G]GTGGACAGGCCAATC | 22937 |
rs60357282 | snp | A/G | 0.138546 | 0.223781 | intron-variant | SCAP | GRCh38.p7 | 3:47421794 | CTGGGGGAAAGACGG[A/G]CGAGAAAAGATGGCA | 22937 |
rs60369822 | snp | A/C | 0.481627 | 0.0940692 | intron-variant | SCAP | GRCh38.p7 | 3:47438245 | TGTTAATTACAGAAA[A/C]CAATTACACAATCTC | 22937 |
rs60634259 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | SCAP | GRCh38.p7 | 3:47437688 | CTGAGGCTGCAATAA[A/G]CCATGATCATGCCAC | 22937 |
rs60723433 | in-del | -/ACACAC | | | intron-variant | SCAP | GRCh38.p7 | 3:47443272 | CACACACACACACAC[-/ACACAC]TCTCTCTCTCTCTCT | 22937 |
rs60750675 | in-del | -/ACACAC | | | intron-variant | SCAP | GRCh38.p7 | 3:47443270 | CACACACACACACAC[-/ACACAC]ACTCTCTCTCTCTCT | 22937 |
rs61738798 | snp | C/T | 4.94197e-05 | 0.00497066 | intron-variant, missense, upstream-variant-2KB, utr-variant-5-prime | SCAP | GRCh38.p7 | 3:47427208 | TAGGAGACCATCCTC[C/T]TCCTGGTGTAGAGGC | 22937 |
rs62248581 | snp | A/C | | | missense | SCAP | GRCh38.p7 | 3:47417427 | CTCGGGGGAGCCACC[A/C]TCGTCCTCAGGGGCC | 22937 |
rs62248582 | snp | A/C | | | intron-variant | SCAP | GRCh38.p7 | 3:47432869 | TCCTCTCTCATTCCC[A/C]GCAAGGTGCTGACAA | 22937 |
rs62248597 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | SCAP | GRCh38.p7 | 3:47446204 | TTTGAGATGGAGTCT[C/T]GCTCTGTCGCCCAGG | 22937 |
rs62248598 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | SCAP | GRCh38.p7 | 3:47467795 | GTTTGTTACATATGC[A/G]TACATGTGCCATGTT | 22937 |
rs62248599 | snp | A/G | 0.482159 | 0.0927485 | intron-variant, upstream-variant-2KB | SCAP, LOC105377073 | GRCh38.p7 | 3:47475238 | CTCCCTGCAACTAAC[A/G]CTATCGTGACATTAT | 22937 |
rs66613198 | in-del | -/A | | | intron-variant | SCAP | GRCh38.p7 | 3:47456791 | CTCCGTCTCAAAAAA[-/A]AAAGATAAATAAGAT | 22937 |
rs67862137 | in-del | -/CT | | | intron-variant | SCAP | GRCh38.p7 | 3:47443307 | CTCTCTCTCTCTCTC[-/CT]TCTCCCTCCCCGCCC | 22937 |
rs67862138 | multinucleotide-polymorphism | CT/TC | 0 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47443307 | CTCTCTCTCTCTCTC[CT/TC]TCTCCCTCCCCGCCC | 22937 |
rs68028519 | in-del | -/ACAT | 0.496714 | 0.0404017 | intron-variant | SCAP | GRCh38.p7 | 3:47435466 | ACATATATAATATAA[-/ACAT]ACACACACACACACA | 22937 |
rs68045711 | in-del | -/TGTA | 0 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47435469 | GTGTGTGTGTGTGTG[-/TGTA]TGTTTATATTATATA | 22937 |
rs71098485 | in-del | -/A/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47437445 | AAAAAAAAAAAAAAA[-/A/T]GGAGAATAAAGTTGG | 22937 |
rs71098488 | in-del | -/T | 0.437118 | 0.165792 | intron-variant | SCAP | GRCh38.p7 | 3:47465848 | GCCACTGCACCCAGC[-/T]TTTTTTTTTTTTGTT | 22937 |
rs71328936 | snp | G/T | 0.5 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47450512 | TGATTATATGCAGGG[G/T]TTTTTTTTTTTTTTC | 22937 |
rs71328937 | snp | A/G | 0.5 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47466157 | AAAAAAAAAAAAAAA[A/G]GAAAGAAATTCTCCC | 22937 |
rs71328938 | snp | A/G | 0.5 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47466161 | AAAAAAAAAAAAGAA[A/G]GAAATTCTCCCCATT | 22937 |
rs71619682 | in-del | -/T | 0.5 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47440598 | TACAAGGCCAGGTTT[-/T]GGTGGCTCACACCTG | 22937 |
rs71619683 | in-del | -/G | 0.5 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47452893 | GGAAAGTTCAACACC[-/G]AGCCTGGGCAACATA | 22937 |
rs72163761 | in-del | -/AT | | | intron-variant | SCAP | GRCh38.p7 | 3:47435468 | ATATATAATATAAAC[-/AT]ACACACACACACACA | 22937 |
rs72297266 | in-del | -/AC | | | intron-variant | SCAP | GRCh38.p7 | 3:47435470 | ATATAATATAAACAT[-/AC]ACACACACACACACA | 22937 |
rs72381717 | in-del | -/TAA | 0.5 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47472471 | ATAAAATAATAATAA[-/TAA]TAATAATAATAATTA | 22937 |
rs72443141 | in-del | -/AAAA | | | intron-variant | SCAP | GRCh38.p7 | 3:47473081 | CGAAACTCCATCTCA[-/AAAA]AAAAAAAAAAAAAAA | 22937 |
rs72911287 | snp | A/G | 0.138546 | 0.223781 | intron-variant | SCAP | GRCh38.p7 | 3:47431491 | AGGAAACCACGTTAC[A/G]TTTAGCTGTAGTGTC | 22937 |
rs72913103 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | SCAP | GRCh38.p7 | 3:47454748 | GACTCTGTCTCAAAA[A/T]ATAATAATAAAAAAA | 22937 |
rs72913106 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | SCAP | GRCh38.p7 | 3:47460363 | AAAGGAAATATTAAC[G/T]ATTTATGTTCAGAGA | 22937 |
rs72913112 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | SCAP | GRCh38.p7 | 3:47466979 | GCACCTGTAGTTTCA[C/G]CTACTTGAGAGGCTG | 22937 |
rs73079273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47434041 | ACCTTCATAGGCAGA[A/G]CCTCATGAAGCCAGG | 22937 |
rs73079289 | snp | G/T | 0.0267878 | 0.112589 | intron-variant | SCAP | GRCh38.p7 | 3:47448559 | GCTCTGTTCATTTTT[G/T]TTTTTCATTTTATTT | 22937 |
rs73081205 | snp | A/C | 0.480539 | 0.0967035 | upstream-variant-2KB, intron-variant | SCAP, LOC105377073 | GRCh38.p7 | 3:47476180 | TCAAGAACTTGCAGA[A/C]AGCCGGGCACGGTGG | 22937 |
rs73834308 | snp | A/G | 0.00155254 | 0.0278184 | synonymous-codon | SCAP | GRCh38.p7 | 3:47419582 | CATGCCACTAGGCAC[A/G]GGCATGGGAGCCAGG | 22937 |
rs73834311 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SCAP | GRCh38.p7 | 3:47430288 | TAAATATCACATACT[C/T]TTCTCACTAGAATCT | 22937 |
rs73834323 | snp | G/T | 0.00597247 | 0.0543191 | upstream-variant-2KB, intron-variant | SCAP, LOC105377073 | GRCh38.p7 | 3:47477946 | AATAGAGAGCATTCA[G/T]GGGAACTTACCTACA | 22937 |
rs74373361 | snp | C/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | SCAP, LOC105377073 | GRCh38.p7 | 3:47476403 | GAGGTCGAGGCCACA[C/G]TGAGACAAAAAACAA | 22937 |
rs74433472 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | SCAP | GRCh38.p7 | 3:47454792 | TATAAAAAATAAATA[C/T]AGACTTCAACTAAAT | 22937 |
rs74477758 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | SCAP | GRCh38.p7 | 3:47428976 | TTTCCACTGCCATGT[C/T]TCATACTAACTCCCC | 22937 |
rs74722963 | snp | C/T | 0.0138799 | 0.0821421 | upstream-variant-2KB, intron-variant | SCAP, LOC105377073 | GRCh38.p7 | 3:47476755 | GAGGCTGCCTCCCCT[C/T]GAGGGAAACACAGGT | 22937 |
rs74848259 | snp | A/T | 0.5 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47438819 | GGGAGACCCTGTCTC[A/T]AAAAAAAAAAAAAAA | 22937 |
rs75061392 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | SCAP | GRCh38.p7 | 3:47436969 | TTCATTCTACTTATA[C/T]ACTCTTTTGTGACTG | 22937 |
rs75114530 | snp | C/T | 0.00340876 | 0.0411432 | synonymous-codon | SCAP | GRCh38.p7 | 3:47418357 | AAGCGGCACGATCTC[C/T]GTCTCGGGTGGCGCA | 22937 |
rs75262220 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant | SCAP | GRCh38.p7 | 3:47454065 | AATTCAACCCTCATC[C/G]TTTTAAGATAAGAAT | 22937 |
rs75385785 | snp | G/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47434774 | CCCGGGAGGCGGAGG[G/T]TGCAGTGAGCCGAGA | 22937 |
rs75715507 | snp | A/C | 0 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47465770 | CAAGACTCCGTCTCA[A/C]AAAAAAAAAAAGAAT | 22937 |
rs75738169 | snp | C/T | 0.00184892 | 0.0303486 | intron-variant | SCAP | GRCh38.p7 | 3:47442840 | GTCCTAAGACACTGG[C/T]CCACCATATCCAAGG | 22937 |
rs75778617 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SCAP | GRCh38.p7 | 3:47427877 | TTTCAAAGTGCATCT[C/G]AAGCCCAAAAGCCCA | 22937 |
rs75867493 | snp | C/T | 0.138207 | 0.223612 | intron-variant | SCAP | GRCh38.p7 | 3:47434705 | AGTTGGGCGTGGTGG[C/T]GCACACCTACAGTCC | 22937 |
rs75909003 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant, upstream-variant-2KB | SCAP | GRCh38.p7 | 3:47425779 | GGACACAGTACACCT[C/T]TTAGGAACCCTAACC | 22937 |
rs75911038 | snp | A/C | 0.5 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47446775 | AGACCGTGTCTTTAC[A/C]AAAAAAAAAACATTA | 22937 |
rs75974312 | snp | G/T | 0.5 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47463349 | TTCATTCCTGCCTCA[G/T]TCCATCCTCGATAAA | 22937 |
rs75986930 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | SCAP | GRCh38.p7 | 3:47426290 | TGTTGAAAGGGAACT[A/T]CTCTATGGTGCCTGA | 22937 |
rs76174845 | snp | C/G | | | intron-variant | SCAP | GRCh38.p7 | 3:47469476 | AACAATTCTTCCTCA[C/G]CTTCCCAAGTAGCTA | 22937 |
rs76221276 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SCAP | GRCh38.p7 | 3:47451143 | CAGACATGAGCCACC[A/G]TGCAAGACTATTTTA | 22937 |
rs76310257 | snp | A/C | 0.5 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47466139 | TGTCTTAAAAACCAA[A/C]AAAAAAAAAAAAAAA | 22937 |
rs76348685 | snp | A/G | 0.5 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47465852 | AAAACAAAAAAAAAA[A/G]AGCTGGGTGCAGTGG | 22937 |
rs76537813 | in-del | -/TTT | | | upstream-variant-2KB, intron-variant | SCAP, LOC105377073 | GRCh38.p7 | 3:47478792 | CCTTTTTTTTTTTTT[-/TTT]GAGACCAAGTCTCTG | 22937 |
rs76558868 | snp | A/G | 0.307671 | 0.243257 | intron-variant | SCAP | GRCh38.p7 | 3:47454974 | GACAAAGAAAACATA[A/G]GTATACAACTGGAAA | 22937 |
rs76729480 | snp | A/C | 0.5 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47466137 | ACTGTCTTAAAAACC[A/C]AAAAAAAAAAAAAAA | 22937 |
rs76790199 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | SCAP | GRCh38.p7 | 3:47431450 | GTTTTTGCCTAATGT[C/T]CTTTTTCTTTTCCAG | 22937 |
rs76861374 | snp | C/G | | | intron-variant | SCAP | GRCh38.p7 | 3:47445406 | TGCCCGCCACTACGC[C/G]CAGCTATTTTTTCGT | 22937 |
rs77215549 | snp | A/C | 0.0283406 | 0.115616 | intron-variant | SCAP | GRCh38.p7 | 3:47419974 | CCCTGAGGTTTGACA[A/C]AGAATGTCCCCACCC | 22937 |
rs77413222 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | SCAP | GRCh38.p7 | 3:47452861 | GGGACACTGAGGCAG[A/G]AAGACTGCTTGAGGC | 22937 |
rs77481436 | snp | A/G | 0.0543475 | 0.155628 | intron-variant | SCAP | GRCh38.p7 | 3:47464740 | ATCCAGTACTGAAAA[A/G]TTTTAGCCAGAGAAA | 22937 |
rs77522610 | snp | A/G | 0.138546 | 0.223781 | intron-variant | SCAP | GRCh38.p7 | 3:47470841 | CACTCCAGCCTGGGC[A/G]ACAAGAGCAAGACTC | 22937 |
rs77563482 | snp | A/C | 0.5 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47454368 | GTGAGACTCCGTCAC[A/C]AAAAAAAAAGAATAG | 22937 |
rs77725461 | snp | A/C | 0.5 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47454367 | AGTGAGACTCCGTCA[A/C]AAAAAAAAAAGAATA | 22937 |
rs77826254 | in-del | -/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47464386 | TTTGTGTTTTTTTTT[-/T]TAAAGTAGATATTAA | 22937 |
rs77843826 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | SCAP | GRCh38.p7 | 3:47443868 | TGCCGACCCAAGCTA[A/C]ACAAATTGGGCCTCT | 22937 |
rs77852723 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | SCAP | GRCh38.p7 | 3:47443462 | AGGCATTCTTCCCCC[A/C/G]CCTCCTCTATGCACA | 22937 |
rs78157886 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | SCAP | GRCh38.p7 | 3:47449811 | GGTTTCCTTCTCCAA[A/T]TCGCATGCTAACATT | 22937 |
rs78176544 | snp | C/T | 0.5 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47441876 | GATGTTCATCTTTCT[C/T]TTTTTTTTTTTTTTT | 22937 |
rs78187985 | in-del | -/CC | | | intron-variant | SCAP | GRCh38.p7 | 3:47466135 | AGACTGTCTTAAAAA[-/CC]AAAAAAAAAAAAAAA | 22937 |
rs78227673 | snp | A/G | 0.0263992 | 0.111815 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | SCAP, LOC105377073 | GRCh38.p7 | 3:47475548 | CACCAGGGGCCCGCG[A/G]AGGTCTGGTGGGGAC | 22937 |
rs78373167 | snp | A/G | 0 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47462770 | AAAAAAAAAAAAAAA[A/G]AAAAGAAAGAAAGAA | 22937 |
rs78730223 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47419816 | GCCTGGGGATGGAGA[C/G]AGGACACAGGCCCCA | 22937 |
rs78862663 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | SCAP | GRCh38.p7 | 3:47442535 | TCTTGCACTTAACCA[C/G]GTACTAAAACGAAAC | 22937 |
rs78914974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47462928 | CTACCCTTTCTCCCC[A/G]GGGCTTCTCAGCCTG | 22937 |
rs78968869 | snp | A/C | 0 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47466136 | GACTGTCTTAAAAAC[A/C]AAAAAAAAAAAAAAA | 22937 |
rs79022527 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | SCAP | GRCh38.p7 | 3:47421386 | CCCCACTGAGCCCCC[A/G]CCCTGCTCATGCATC | 22937 |
rs79094378 | in-del | -/AAA | | | intron-variant | SCAP | GRCh38.p7 | 3:47437586 | TCCCTAAAAAAAAAA[-/AAA]TACAAAAGTTAGCCA | 22937 |
rs79375145 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | SCAP | GRCh38.p7 | 3:47464481 | ATTAAGGTAATATGC[C/T]ACATTACTAGAATGA | 22937 |
rs79382394 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | SCAP | GRCh38.p7 | 3:47449596 | ACGAGATTTCTTCCT[C/G]CATCCCCATTCCTGA | 22937 |
rs79594451 | in-del | -/A | | | intron-variant | SCAP | GRCh38.p7 | 3:47465842 | CTTGTTTAAAAAAAC[-/A]AAAAAAAAAAAGCTG | 22937 |
rs79639552 | snp | C/T | 0.000776442 | 0.019688 | intron-variant, upstream-variant-2KB | SCAP | GRCh38.p7 | 3:47427301 | CTGACACAGAAATGA[C/T]AGCTACTGCAGAGCC | 22937 |
rs80017429 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SCAP | GRCh38.p7 | 3:47445069 | GAGGCACCGAGCCCA[A/G]CCACTTCATTACTTT | 22937 |
rs80132823 | in-del | -/CTTTTTTTTT | | | intron-variant | SCAP | GRCh38.p7 | 3:47416615 | GTCACACCCCTAACG[-/CTTTTTTTTT]TTTTTTTTTTTTTTT | 22937 |
rs80169713 | snp | A/C | | | intron-variant | SCAP | GRCh38.p7 | 3:47455426 | ATGGTGAAACCCCGT[A/C]TCTACTAAAAATACA | 22937 |
rs80214365 | snp | C/T | 0.5 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47432602 | AGGAAGTTTTGGCTC[C/T]TTCGTATAGGCAGCA | 22937 |
rs80223072 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | SCAP | GRCh38.p7 | 3:47464489 | AATATGCCACATTAC[C/T]AGAATGAAGGAGAAA | 22937 |
rs80292687 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SCAP | GRCh38.p7 | 3:47458695 | ACCAACAAACCTATT[A/G]AAGATTTTCTTCCAC | 22937 |
rs111296734 | snp | C/T | 0.5 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47462850 | TGATGTCCTAGAAGG[C/T]TGTGCTTCTCAGCCT | 22937 |
rs111328787 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SCAP | GRCh38.p7 | 3:47435738 | AACACCAACATGTTA[C/T]AATATATAACATTAT | 22937 |
rs111414660 | snp | C/T | 0.5 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47448484 | CTCTTTCTCCTCTCT[C/T]TTTGAGACTTCAAAA | 22937 |
rs111421299 | snp | C/T | 0.5 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47427870 | GTCTGACTTTCAAAG[C/T]GCATCTGAAGCCCAA | 22937 |
rs111539100 | in-del | -/GAGAAT | 0.0865458 | 0.189163 | intron-variant | SCAP | GRCh38.p7 | 3:47438429 | GAGAAACGACTACAA[-/GAGAAT]AGTGATCAGAATTCA | 22937 |
rs111640036 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | SCAP, LOC105377073 | GRCh38.p7 | 3:47478324 | TGTGCCTTGAAGCAT[A/G]GCAAACAATCCTCCA | 22937 |
rs111695253 | in-del | -/T | 0.5 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47444787 | CCAGTACTTCATTAC[-/T]TTTTTTTTTTTTGAG | 22937 |
rs111729862 | snp | C/G | | | intron-variant | SCAP | GRCh38.p7 | 3:47431941 | TTTATATTTATTCAA[C/G]CATATGGACTCAGGA | 22937 |
rs111762817 | snp | C/T | 0.127599 | 0.217986 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | SCAP, LOC105377073 | GRCh38.p7 | 3:47475926 | CCTCCCTCTCTCTCC[C/T]GGCCGCCGGGTGCCC | 22937 |
rs111776889 | snp | A/T | 0 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47438431 | AGAAACGACTACAAG[A/T]GATCAGAATTCATTT | 22937 |
rs111802076 | snp | A/C | 0.5 | 0 | upstream-variant-2KB, intron-variant | SCAP, LOC105377073 | GRCh38.p7 | 3:47479092 | AATATGAAAACATAA[A/C]AGAAAAGTTGAAAGA | 22937 |
rs111814409 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47468951 | ATGGCTCCTGGATCG[A/G]TAGTTTCTATGTAGA | 22937 |
rs111955430 | snp | C/T | | | missense | SCAP | GRCh38.p7 | 3:47418407 | GCAGCTCCCCGCGCC[C/T]CCGCCGCCCGGGCCC | 22937 |
rs112015701 | snp | A/G | 0.5 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47463203 | TAGGAAACATCCTAC[A/G]ACAAGCCCACATCTG | 22937 |
rs112034859 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SCAP | GRCh38.p7 | 3:47453712 | TGTAATACGCCCCCA[G/T]GTTACCCATCTAGAA | 22937 |
rs112119934 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | SCAP | GRCh38.p7 | 3:47432614 | CTCCTTCGTATAGGC[A/G]GCAGATGCCTGCAAT | 22937 |
rs112299119 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SCAP | GRCh38.p7 | 3:47457463 | ATCACCTTGTGTTCC[A/C]TAGAGCACCCAGCAC | 22937 |
rs112333807 | snp | C/G | 0 | 0 | upstream-variant-2KB, intron-variant | SCAP, LOC105377073 | GRCh38.p7 | 3:47478493 | ATTTTTTTTTTTTGA[C/G]ACACAGTCTCATTCT | 22937 |
rs112560350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SCAP | GRCh38.p7 | 3:47426726 | CAGGCGTGAGCCACC[A/G]CGCCCGGCCTCCAAC | 22937 |
rs112741837 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | SCAP | GRCh38.p7 | 3:47464921 | AATTCAACAAAGTTG[C/T]AGGATGCAAAATGAA | 22937 |
rs112758946 | snp | C/T | 0.5 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47459575 | ACCGTGATACCCACC[C/T]GAGCTGCAAAACCAG | 22937 |
rs112830289 | snp | A/G | 0.0120495 | 0.0766784 | downstream-variant-500B, synonymous-codon | PTPN23, SCAP | GRCh38.p7 | 3:47413929 | GCAGACAATGGCAGC[A/G]TTGTCCAGCACCAGG | 22937 |
rs112833043 | snp | A/G | 0.000105066 | 0.0072472 | intron-variant | SCAP | GRCh38.p7 | 3:47417261 | AGGCCCACAATCCCC[A/G]GGGCGGACAGCCGCT | 22937 |
rs112915683 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47466807 | TAAAAACTTTTGGCC[A/G/T]GGCGTGGTGGCTCAC | 22937 |
rs112933622 | snp | C/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47447995 | GGGCAAGAGGGAGAC[C/T]CCGTCTCAAAAAAAA | 22937 |
rs113000966 | snp | C/T | 0.00127561 | 0.0252225 | intron-variant | SCAP | GRCh38.p7 | 3:47418617 | ACCCGTCCCCCTCCC[C/T]GCACTCTTTCCCACC | 22937 |
rs113001398 | snp | A/G | 0.5 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47417014 | CCAAGAAGGTCAATC[A/G]AATCATACAGTACAG | 22937 |
rs113175900 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | SCAP | GRCh38.p7 | 3:47460660 | GCCCCCAGGTTCAAG[C/T]GATTCTCCTGCCTCA | 22937 |
rs113251658 | snp | C/G | 0.401747 | 0.198678 | intron-variant | SCAP | GRCh38.p7 | 3:47417890 | AGAGGGGGCGGGGGA[C/G]GGGGGTGAGAGGGGG | 22937 |
rs113336860 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SCAP | GRCh38.p7 | 3:47422114 | GCACAGCCAGTCCCC[A/G]GCTCCTGCCATGCCC | 22937 |
rs113398477 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | SCAP | GRCh38.p7 | 3:47426894 | CCTGCCCTAGGCTCA[A/G]GAGAGACCAGAGGAG | 22937 |
rs113635329 | snp | A/G | 0 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47421764 | CACCCCCATCCCTCA[A/G]CTGGCCTGCCAGCCC | 22937 |
rs113725418 | snp | C/T | 0.5 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47420294 | CAACTAACAGGCTCC[C/T]GTCCTGGGCCACTCT | 22937 |
rs113753925 | snp | A/G | | | intron-variant | SCAP | GRCh38.p7 | 3:47459777 | ATTGTCTTGATAAAC[A/G]TCTTAAACAACAGAA | 22937 |
rs113848929 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | SCAP, LOC105377073 | GRCh38.p7 | 3:47474558 | CCAACACTTTGGGAG[C/G]CCAAGGCTTGTATAA | 22937 |
rs113909034 | snp | A/G | 0.5 | 0 | intron-variant, missense, utr-variant-5-prime | SCAP | GRCh38.p7 | 3:47427629 | GGCAGCAGGTCGGTC[A/G]CTTGCAGACACAACT | 22937 |
rs113945636 | snp | A/G | | | intron-variant | SCAP | GRCh38.p7 | 3:47448017 | CAAAAAAAAAAAAAA[A/G]AAAAAAAAAAAAAAA | 22937 |
rs114141882 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SCAP | GRCh38.p7 | 3:47442112 | CCTTCAGCATAGCAC[C/T]GAAAACATCTATAAA | 22937 |
rs114537398 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SCAP | GRCh38.p7 | 3:47421277 | GAAGGGGAAGTACCT[C/T]CCCTGAATCTTCCGG | 22937 |
rs114541375 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | SCAP | GRCh38.p7 | 3:47437585 | ATCCCTAAAAAAAAA[A/C]AAATACAAAAGTTAG | 22937 |
rs114663663 | snp | A/G | 0.00478085 | 0.0486577 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | SCAP, LOC105377073 | GRCh38.p7 | 3:47477030 | AGTCACCAATGCAAG[A/G]CAGAAATTAGAGGTG | 22937 |
rs114849033 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SCAP | GRCh38.p7 | 3:47449697 | TCCAGCACACATTTC[C/T]AGGTTTGGGGCTGAC | 22937 |
rs114974019 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SCAP | GRCh38.p7 | 3:47439148 | GCAAGGTGGCTTATG[C/T]CTATAATCCCAGGAC | 22937 |
rs115028044 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | SCAP | GRCh38.p7 | 3:47430368 | CACATATGCAACCCT[C/G]AGTAACAGGCATGTC | 22937 |
rs115218053 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SCAP | GRCh38.p7 | 3:47461192 | TGGGCTCACAAACCT[A/G]AGTGCTATGGGTTCT | 22937 |
rs115332706 | snp | A/G | 0.00587121 | 0.0538622 | intron-variant | SCAP | GRCh38.p7 | 3:47418852 | GATGTACCTGGATTC[A/G]GACAGTGGGCAGCCT | 22937 |
rs115332909 | snp | C/T | 0.00438332 | 0.0466095 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | SCAP, LOC105377073 | GRCh38.p7 | 3:47477048 | GAAATTAGAGGTGGC[C/T]CTTCTGACCGCACCA | 22937 |
rs115383061 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | SCAP | GRCh38.p7 | 3:47422612 | CAACCTCATGGGCCT[C/T]GGAGTGGCAGAGGCA | 22937 |
rs115782441 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SCAP | GRCh38.p7 | 3:47422369 | GAGGGGAGCACCCTG[C/T]CCATGGCTGCACAGC | 22937 |
rs115945419 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47428030 | AAAATATCTGTCAAC[A/G]CCACTAGCTAACTAA | 22937 |
rs116279218 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SCAP | GRCh38.p7 | 3:47456858 | GGTGCTAAATTCCCG[C/T]GTATATAAGCAATTT | 22937 |
rs116353390 | snp | A/G | 0.0655868 | 0.168795 | intron-variant | SCAP | GRCh38.p7 | 3:47469288 | GGAGGCAAAGGTTGC[A/G]GTGAGCAGAGACCAC | 22937 |
rs116395559 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SCAP | GRCh38.p7 | 3:47423126 | ATCACAGAGGCTCAC[A/G]GAGGTCTGGATGAAT | 22937 |
rs116558279 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | SCAP | GRCh38.p7 | 3:47432965 | TAGCCAACTGGGCTC[C/G]CTTTTATCCTCCACT | 22937 |
rs116616542 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SCAP | GRCh38.p7 | 3:47428029 | CAAAATATCTGTCAA[C/T]GCCACTAGCTAACTA | 22937 |
rs116779483 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SCAP | GRCh38.p7 | 3:47437860 | GCACTTATTTCTGTC[A/G]GGTATATTCCTAGGA | 22937 |
rs116924117 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SCAP | GRCh38.p7 | 3:47446765 | GGACACTGTGAGACC[A/G]TGTCTTTACAAAAAA | 22937 |
rs117238604 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SCAP, LOC105377073 | GRCh38.p7 | 3:47475259 | GTGACATTATAAGCC[C/G]GTTAAATACTGAGGT | 22937 |
rs117610268 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SCAP | GRCh38.p7 | 3:47447298 | CCCAGCTACTTGGTA[C/T]GCTGAGAATCACCTG | 22937 |
rs117826902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47468972 | TCTATGTAGAATAAT[A/G]AAAACATTCTGGAAA | 22937 |
rs117953394 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SCAP | GRCh38.p7 | 3:47428239 | GGCAGGAAGCCATGT[A/G]GGTCATGAGTTAGCA | 22937 |
rs137921285 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SCAP | GRCh38.p7 | 3:47441337 | GCCAAGTGTGGTGGC[A/G]CACACCTGTGGTTGT | 22937 |
rs137940863 | snp | A/G | 1.65614e-05 | 0.00287757 | missense | SCAP | GRCh38.p7 | 3:47414026 | TTTAGGTCCCAAAAG[A/G]AGACACAGCCCTGGC | 22937 |
rs137941299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47444339 | AAAGATGACTCCTCA[C/T]AAGTGTCAAGATCAG | 22937 |
rs137985341 | snp | A/G | 0.0197687 | 0.0974348 | upstream-variant-2KB, intron-variant | SCAP, LOC105377073 | GRCh38.p7 | 3:47478754 | AAGTGCTGGGATTAC[A/G]GGCGTGAGCCACCTC | 22937 |
rs138055698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47461996 | CTGAGATCACACTGC[C/T]GTACTCCAGCCTGGG | 22937 |
rs138180647 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SCAP | GRCh38.p7 | 3:47447801 | CTCCTGAGGTCAGGA[A/G]TTCAAGACCAGCCTG | 22937 |
rs138205444 | snp | A/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47472458 | AAAAAAAAAATAAAA[A/T]AAAATAATAATAATA | 22937 |
rs138212747 | snp | C/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47453254 | CCTAAAATAAAGACC[C/T]GCTTATGGCCAGGCA | 22937 |
rs138296178 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | SCAP | GRCh38.p7 | 3:47429503 | AGGTGTGTGCACCAC[C/G]ACCACGCCTAATTTT | 22937 |
rs138330271 | snp | A/G/T | 5.00597e-05 | 0.00500273 | missense | SCAP | GRCh38.p7 | 3:47420706 | GCTCGTAGCGCGTTG[A/G/T]CTGTCCCACTGGCTT | 22937 |
rs138331328 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SCAP | GRCh38.p7 | 3:47466721 | AAGATCTTCATGATG[C/T]TGAGTTTAGCAAGGA | 22937 |
rs138393381 | snp | C/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47455428 | GGTGAAACCCCGTCT[C/T]TACTAAAAATACAAA | 22937 |
rs138431688 | snp | A/G | | | intron-variant | SCAP | GRCh38.p7 | 3:47452627 | CCTATCCCAGACCTG[A/G]TGAATCAGAAAATCT | 22937 |
rs138475750 | snp | A/G | 0.000235618 | 0.0108514 | synonymous-codon | SCAP | GRCh38.p7 | 3:47418184 | CTGCGCGTCCCACAC[A/G]CAGACGTGGCCTGCC | 22937 |
rs138517622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47467651 | CAACAAAAAAGAAGA[C/T]ATACAAATGGCCAAT | 22937 |
rs138542218 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | SCAP, LOC105377073 | GRCh38.p7 | 3:47474507 | ATTTTAAAAGATACA[A/G]GTCTTGGCCGGGCAC | 22937 |
rs138591267 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SCAP | GRCh38.p7 | 3:47434046 | CATAGGCAGAGCCTC[A/G]TGAAGCCAGGGTGGT | 22937 |
rs138628590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47458845 | AGTTTTGCTCTTGTT[A/G]CCCAGGCTGACGTGC | 22937 |
rs138723907 | snp | A/G | 1.68525e-05 | 0.00290275 | missense | SCAP | GRCh38.p7 | 3:47414928 | CTGTGTGGGTCAGGT[A/G]ACAGGCCACTGTGTC | 22937 |
rs138855874 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | SCAP | GRCh38.p7 | 3:47415544 | GGGCTGCTGAGGGGA[A/C]ACAGGATGCAGGGTG | 22937 |
rs138870302 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47420241 | GAACCCGACCCAGGG[C/T]AATGTGGTGGCCACA | 22937 |
rs138982814 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SCAP | GRCh38.p7 | 3:47440448 | TGGAGGCTGAGAGAC[C/T]TCACCCAGCCTTGGA | 22937 |
rs139054902 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SCAP | GRCh38.p7 | 3:47470111 | CCTAAAATATTTACA[C/T]GCTGCAAATTATTTT | 22937 |
rs139075380 | snp | A/C/G | 2.59077e-05 | 0.00359907 | synonymous-codon | SCAP | GRCh38.p7 | 3:47417415 | AGGGGAGCCTTTCTC[A/C/G]GGGGAGCCACCCTCG | 22937 |
rs139088515 | snp | A/G | | | intron-variant | SCAP | GRCh38.p7 | 3:47430786 | TGTGGACTGAAGGGG[A/G]CAGGGCCCAGCCCAG | 22937 |
rs139126586 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47434521 | AGGAGGAGTGGGCTG[C/G]GGTCAGGAGACCTAG | 22937 |
rs139126796 | snp | G/T | 0.000155988 | 0.00883004 | missense | SCAP | GRCh38.p7 | 3:47418208 | GCCTGCCAGGCAGCA[G/T]CTCACCAGCAGCATG | 22937 |
rs139135816 | snp | A/C/G | 0.000232792 | 0.0107863 | missense, intron-variant, upstream-variant-2KB | SCAP | GRCh38.p7 | 3:47426122 | CGAAGGCTGCAGTTG[A/C/G]GGCTGGGGTGCAGAA | 22937 |
rs139156863 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | SCAP, LOC105377073 | GRCh38.p7 | 3:47476771 | GAGGGAAACACAGGT[C/T]CCCACCTGCCCAGCT | 22937 |
rs139183745 | in-del | -/GCCCC | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | PTPN23, SCAP | GRCh38.p7 | 3:47413805 | GGTTCAGTGCATTGG[-/GCCCC]CCCCCACACAGCACC | 22937 |
rs139280167 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant, upstream-variant-2KB | SCAP, LOC105377073 | GRCh38.p7 | 3:47474782 | AGCCTGGGAGACAGA[A/G]TGAGACCCTGTCTCC | 22937 |
rs139360994 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SCAP | GRCh38.p7 | 3:47428799 | AACCAATGACTAATA[C/T]AAGTTCTTGAGTTTG | 22937 |
rs139371188 | snp | C/G | 1.77376e-05 | 0.002978 | intron-variant, missense, utr-variant-5-prime | SCAP | GRCh38.p7 | 3:47427662 | TCCAAGCTCCTGATC[C/G]CAGAGCTGCACAGGA | 22937 |
rs139482402 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47423880 | CAGCAAGAGGAACAG[A/G]CCCCATTCCAGCCCC | 22937 |
rs139512391 | snp | C/T | 0.119281 | 0.213102 | intron-variant | SCAP | GRCh38.p7 | 3:47455517 | GGAGAATCACTTGAA[C/T]CTGGGAGGTGGAGGT | 22937 |
rs139566246 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | SCAP | GRCh38.p7 | 3:47448312 | TTAATCTTTTATCCT[C/G]CAACTGTCCTGAAAT | 22937 |
rs139599229 | snp | A/C | 0.000153988 | 0.00877328 | downstream-variant-500B, synonymous-codon | PTPN23, SCAP | GRCh38.p7 | 3:47413872 | GTCCAGCTTCTCCAG[A/C]ACAGAGGGCACATAC | 22937 |
rs139623859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47442185 | AAAAGAATAAGATGG[A/G]CTCTTTTCACAGCTG | 22937 |
rs139700112 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | SCAP | GRCh38.p7 | 3:47442525 | CAAAAAAGGCTCTTG[A/C]ACTTAACCAGGTACT | 22937 |
rs139812346 | snp | C/G | 0.00597247 | 0.0543191 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | SCAP, LOC105377073 | GRCh38.p7 | 3:47476020 | AGCGGCGTGCGCATG[C/G]GTAGTCGAACCACAT | 22937 |
rs139824337 | snp | C/T | 6.60807e-05 | 0.0057477 | synonymous-codon | SCAP | GRCh38.p7 | 3:47422493 | GATGATGCCCAGCTC[C/T]GTGGCCATGTTCTTC | 22937 |
rs139943406 | snp | A/G | 0.00130214 | 0.0254828 | utr-variant-5-prime, synonymous-codon | SCAP | GRCh38.p7 | 3:47442883 | ATACCAGCAGGCTAA[A/G]ATGCAGAACCCTGTG | 22937 |
rs139953069 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SCAP | GRCh38.p7 | 3:47460268 | CAGCTTACGAAGATA[A/G]CAGGATTAAGAGATT | 22937 |
rs140088473 | in-del | -/GAAG | 0.00438332 | 0.0466095 | intron-variant | SCAP | GRCh38.p7 | 3:47424650 | CTCTGCTTTGGAGCC[-/GAAG]GAAGGGAGGGCCCTG | 22937 |
rs140110185 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SCAP | GRCh38.p7 | 3:47463514 | TGAGACCAGCCTGGC[C/T]AACATAGTGAAACCT | 22937 |
rs140158026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47457591 | CTGAAAGTTGTCAAG[C/T]GGACCAATGCTAAGG | 22937 |
rs140351961 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47461872 | AACCCTATCTCTACT[A/T]AAAATACAAAAATTA | 22937 |
rs140372128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47424685 | GAAGGGTATGGCAGA[C/T]GGTATGGGGGAGGGT | 22937 |
rs140453174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47473820 | CTGAATCGCATATGC[C/T]TCCATTTTTCTAGTA | 22937 |
rs140472469 | snp | A/G | 1.65241e-05 | 0.00287433 | intron-variant | SCAP | GRCh38.p7 | 3:47420914 | GGCGGGCAGGGCAGG[A/G]CTCAGCCCACTCCTA | 22937 |
rs140844740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47431486 | CATCCAGGAAACCAC[A/G]TTACGTTTAGCTGTA | 22937 |
rs140861904 | snp | A/C/T | 0.00698089 | 0.0586676 | synonymous-codon | SCAP | GRCh38.p7 | 3:47414632 | GGTGAAGAGGCAGCA[A/C/T]GAGTCCTCCAGACGG | 22937 |
rs140886519 | snp | C/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47455342 | GCTCACGCCTGTAAT[C/T]TCAGCAACTTGGGAG | 22937 |
rs140916562 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | SCAP | GRCh38.p7 | 3:47469090 | CGTTGGCTCACACCT[A/G]CAATCCCAGCACTTG | 22937 |
rs140916813 | snp | C/T | 0.00835141 | 0.0640778 | utr-variant-3-prime, downstream-variant-500B | PTPN23, SCAP | GRCh38.p7 | 3:47413438 | ACCCTGTTCTGTGGC[C/T]CGTGTCTGAGTCTGC | 22937 |
rs140954403 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SCAP | GRCh38.p7 | 3:47416311 | GAGTGTGCATGCAGA[C/T]GGAGTACTGGGGACG | 22937 |
rs141033707 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47466511 | ACAAATATAATCAAC[G/T]GATTTTTGACAAAGA | 22937 |
rs141039095 | snp | C/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47452208 | TAAATAAACTCCCTG[C/T]CTGTTCTTCAGGGTC | 22937 |
rs141103117 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | SCAP | GRCh38.p7 | 3:47456819 | GATCTGGAAAAATAC[-/A]ACTGCAATTCATATC | 22937 |
rs141245171 | snp | C/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47454560 | GGTGAAACCCCCGTC[C/T]CCACTAAAAAATACA | 22937 |
rs141274204 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | SCAP | GRCh38.p7 | 3:47466858 | GGAAGCCAAGGCAAG[A/C]GGACTGCTTGAGCTC | 22937 |
rs141329048 | snp | A/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47472455 | CAAAAAAAAAAAATA[A/T]AATAAAATAATAATA | 22937 |
rs141351370 | snp | C/T | 0.00103335 | 0.022707 | synonymous-codon | SCAP | GRCh38.p7 | 3:47419549 | GGAGAAGGCAGGGTC[C/T]GGGTGGCTGGGGGGC | 22937 |
rs141530309 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SCAP, LOC105377073 | GRCh38.p7 | 3:47478674 | TAGAGACAGAGTTTC[A/G]CCATGTTGGCCAGGC | 22937 |
rs141535771 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SCAP | GRCh38.p7 | 3:47432706 | TTTTAGAGACAAGGT[C/T]TCACTCTATTGCCCC | 22937 |
rs141576521 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47438041 | GTCAGTCCAATTAAT[A/G]TTAACCATTTAGAGG | 22937 |
rs141602402 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SCAP | GRCh38.p7 | 3:47463395 | AATCACTAATGTCAC[C/T]ACCCTGCTCAAAACA | 22937 |
rs141634921 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | SCAP, LOC105377073 | GRCh38.p7 | 3:47475528 | CCGCGCATCTCCCCC[C/G]GTCACACCAGGGGCC | 22937 |
rs141636890 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SCAP | GRCh38.p7 | 3:47441389 | GGGAGGGTCGCTTGA[A/G]CCTAGGAGGTTGAGG | 22937 |
rs141687171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47434079 | ACTCCCCACTGACAC[C/T]ATGTATAGTTGTGCC | 22937 |
rs141739155 | snp | C/T | 0.000558825 | 0.0167063 | intron-variant | SCAP | GRCh38.p7 | 3:47415080 | GTGTGAACACCTGCC[C/T]ACCCCAGGCCCTCCG | 22937 |
rs141804213 | snp | A/G | 0.000910483 | 0.021317 | synonymous-codon | SCAP | GRCh38.p7 | 3:47422451 | CCTTACCTGGATGGC[A/G]GGCACTAGGGTGAAG | 22937 |
rs141943007 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | SCAP | GRCh38.p7 | 3:47458498 | TGAACGAAAGCTGAT[G/T]TCAGAGAATTTAAAG | 22937 |
rs141958520 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SCAP | GRCh38.p7 | 3:47433499 | CATTAAACATCTATT[C/T]CACACCAATGGGCCA | 22937 |
rs141980115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47461671 | TCCAACTCCCAGCCC[A/G]GGGAACATTTCCATG | 22937 |
rs142031657 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | SCAP | GRCh38.p7 | 3:47416228 | GAAGGCACCTGGCCA[C/G]TGGGTGGAGACCCAG | 22937 |
rs142087467 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47459402 | TGACGAGTCTCGTTG[C/T]GTTACTACTTCAATA | 22937 |
rs142124298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47440561 | TTTGGGAAAATAAGT[A/G]CACAGCACTAAGAAT | 22937 |
rs142134807 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SCAP | GRCh38.p7 | 3:47469491 | GCTTCCCAAGTAGCT[A/G]GAATTACAGGTGCGT | 22937 |
rs142171701 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SCAP | GRCh38.p7 | 3:47437213 | GGGAGGCTGAGGCAG[A/G]TGGATCACCTGAGAT | 22937 |
rs142311061 | snp | C/T | 5.59227e-05 | 0.00528755 | missense | SCAP | GRCh38.p7 | 3:47417698 | GGCGGCGGAGGGCCC[C/T]GGGGGCGGTGTCTCA | 22937 |
rs142327684 | snp | C/G | 1.67688e-05 | 0.00289554 | utr-variant-5-prime, missense | SCAP | GRCh38.p7 | 3:47435127 | GCAAGGGGAGTTTCA[C/G]CAGTGGGTAGCTGGG | 22937 |
rs142333961 | snp | C/G | 0.02016 | 0.0983543 | upstream-variant-2KB, intron-variant | SCAP, LOC105377073 | GRCh38.p7 | 3:47477537 | GATCATGCCACTGCA[C/G]TCCAGCTTGGGCGAC | 22937 |
rs142353403 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SCAP | GRCh38.p7 | 3:47427320 | TACTGCAGAGCCACC[A/G]AGGACCCCTTTCTCA | 22937 |
rs142360291 | in-del | -/G | 0.0182019 | 0.0936463 | intron-variant | SCAP | GRCh38.p7 | 3:47430261 | AAGGACTCAAACCAA[-/G]GGTCTCCTCACTAAA | 22937 |
rs142390763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47431752 | CACTGCTGCTTTAAC[C/T]CCAATCACTTACTGT | 22937 |
rs142473563 | in-del | -/GT | 0.0547245 | 0.156101 | intron-variant | SCAP | GRCh38.p7 | 3:47419137 | GGCTGGCAGCCACCA[-/GT]GACTCCTCAGAGCAA | 22937 |
rs142490430 | in-del | -/AAA | | | intron-variant | SCAP | GRCh38.p7 | 3:47448003 | GGGAGACTCCGTCTC[-/AAA]AAAAAAAAAAAAAAA | 22937 |
rs142541379 | snp | A/G | 2.27456e-05 | 0.00337228 | synonymous-codon | SCAP | GRCh38.p7 | 3:47418756 | TGGGGGCCAGGCACT[A/G]CGGCCGTCCTGAGGG | 22937 |
rs142544233 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SCAP | GRCh38.p7 | 3:47462013 | TACTCCAGCCTGGGC[A/G]ACAGAGTGAGACTCC | 22937 |
rs142581614 | snp | C/G/T | 0.00139929 | 0.0264141 | intron-variant, synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | SCAP | GRCh38.p7 | 3:47427562 | GAAGTTCCCAGGGGA[C/G/T]AGCAGCAGGCATCCA | 22937 |
rs142588599 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47423375 | GGAGTGAGGCAGTAA[A/G]AGAAAATACTAGGCG | 22937 |
rs142666038 | snp | C/T | 0.000115339 | 0.00759318 | intron-variant, synonymous-codon, utr-variant-5-prime | SCAP | GRCh38.p7 | 3:47428581 | CAAAGGTGAACGAAA[C/T]ACATCTACTGCCAGG | 22937 |
rs142726759 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SCAP | GRCh38.p7 | 3:47465785 | AAAAAAAAAAAAGAA[C/T]ATTGTCTTCCAATCC | 22937 |
rs142742550 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SCAP | GRCh38.p7 | 3:47459947 | CAGAGCGGCCATTTA[C/T]AGACCTCCCACCAGG | 22937 |
rs142752447 | snp | C/T | 0.000501312 | 0.0158242 | missense | SCAP | GRCh38.p7 | 3:47417150 | ACACCAGAGCGGTAA[C/T]GCCTGAGGAGACCTC | 22937 |
rs142781809 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | SCAP | GRCh38.p7 | 3:47462704 | GTTGCAGTGAGCCAA[C/G]ATCGCGCCATTGCAC | 22937 |
rs142809139 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47443113 | AGAAGGGAGAAAAGC[C/G]AGTTAACAAAGAGTA | 22937 |
rs142984933 | snp | C/T | 0.000116012 | 0.00761529 | synonymous-codon, intron-variant, upstream-variant-2KB | SCAP | GRCh38.p7 | 3:47426103 | GTGGACCAGGCTCTC[C/T]GCCCGAAGGCTGCAG | 22937 |
rs143077962 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | SCAP | GRCh38.p7 | 3:47445292 | GCTCTTGTTGCCCAG[A/G]CTGGAGTGCTGTGGC | 22937 |
rs143119656 | snp | C/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47431274 | ACAATCCCTACTTTA[C/T]AGCACAAAGACTGAA | 22937 |
rs143143823 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SCAP | GRCh38.p7 | 3:47424460 | GCTAAATGCAAGGAG[A/G]TGAAACCATCCTGAA | 22937 |
rs143150702 | in-del | -/A | 0.0551013 | 0.156571 | intron-variant | SCAP | GRCh38.p7 | 3:47453379 | AGACCCCATCTCTTT[-/A]AAAAAAAATTTTTAA | 22937 |
rs143174139 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SCAP | GRCh38.p7 | 3:47430384 | AGTAACAGGCATGTC[A/G]CGGAGCACCCCAAAA | 22937 |
rs143230703 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | SCAP | GRCh38.p7 | 3:47422739 | CCACACAGCTGCTAC[G/T]GGGAACGGGTGTTCA | 22937 |
rs143267790 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SCAP | GRCh38.p7 | 3:47428956 | TGCCGATGTCACAGC[C/T]TGAATTTCCACTGCC | 22937 |
rs143302981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47473538 | GCTTCTCTATGAGGA[A/G]TCCTCTCATCTGTTC | 22937 |
rs143381584 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47471834 | TACAGTGATAATACA[C/G]TGTACATTATAAAGT | 22937 |
rs143390952 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SCAP | GRCh38.p7 | 3:47440222 | ACTGAATGTCTAGCA[A/G]AACTACTAGAAGCAG | 22937 |
rs143528422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47459080 | AAAGTACTGGGATTA[C/T]AGGTGTGAGCCACCG | 22937 |
rs143528629 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, nc-transcript-variant | SCAP, LOC105377073 | GRCh38.p7 | 3:47476292 | ACGTAGGAGACCTCC[A/G]TCTCCACAAGTAAAA | 22937 |
rs143598836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47454981 | AAAACATAGGTATAC[A/G]ACTGGAAAGGAAAAA | 22937 |
rs143648811 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47447919 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCCAGGAG | 22937 |
rs143678713 | snp | A/G | 0.000613905 | 0.0175093 | synonymous-codon | SCAP | GRCh38.p7 | 3:47419345 | CTTGGCCAGTGTGAT[A/G]TTGTAATAGCTGAAG | 22937 |
rs143727722 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | SCAP | GRCh38.p7 | 3:47426854 | CAGGCCATATAGGGT[A/G]CTCAGTAGTAACCAG | 22937 |
rs143813308 | in-del | -/C | | | intron-variant | SCAP | GRCh38.p7 | 3:47417268 | AATCCCCGGGGCGGA[-/C]CAGCCGCTCTGCCCA | 22937 |
rs143838773 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47432854 | TCCCTTTGGAAACCA[A/T]CCTCTCTCATTCCCA | 22937 |
rs143928693 | snp | C/T | 1.6546e-05 | 0.00287624 | synonymous-codon | SCAP | GRCh38.p7 | 3:47419384 | CCAGTGGCGGAAGGA[C/T]AATTTCCTCCAAAGT | 22937 |
rs143968318 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47429892 | CCCCAAAGCATGTAA[A/C]CTGTCTTACTGATTC | 22937 |
rs144097981 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47425090 | CTTCTCTATCTCACA[C/T]CTCCAGTGGCTTAAG | 22937 |
rs144166897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47435199 | GTCCTCTCTCAGCAC[C/T]GACACAGGAGCCACT | 22937 |
rs144169656 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SCAP | GRCh38.p7 | 3:47431366 | TTCATCTCTGTAGTC[C/T]TCCTTCTGAAAACCA | 22937 |
rs144277102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47448961 | TTGTTTAAGTCCCAC[A/G]TAAAATTTTGAATTT | 22937 |
rs144348394 | snp | C/T | 0.00279162 | 0.0372561 | downstream-variant-500B | PTPN23, SCAP | GRCh38.p7 | 3:47413539 | ATGGTACCAAACTGC[C/T]ACACTACCAGGACAG | 22937 |
rs144403056 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SCAP | GRCh38.p7 | 3:47451668 | CCTCCCAAAGAGTTG[A/G]GATTACAGGCTGAGC | 22937 |
rs144507733 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SCAP, LOC105377073 | GRCh38.p7 | 3:47475095 | CGACTGTCGCCATAC[A/C]AGGTGGAGCAGTGAG | 22937 |
rs144572130 | snp | C/T | 0.00019816 | 0.00995193 | synonymous-codon | SCAP | GRCh38.p7 | 3:47421027 | AGCAAAGAGACAGAA[C/T]TCCTGGAATCAGAGC | 22937 |
rs144590914 | in-del | -/CCC | | | intron-variant | SCAP | GRCh38.p7 | 3:47422101 | GTGTGACAAACTGCA[-/CCC]CAGCCAGTCCCCAGC | 22937 |
rs144600203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47442490 | AGATACTGTTCTAAT[A/G]GACTTTGCCTCGCAA | 22937 |
rs144655846 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SCAP | GRCh38.p7 | 3:47416003 | TTGGCCAGGCTGGAG[A/G]GGAGGATGTCAGCCA | 22937 |
rs144742739 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47466570 | AGTCTCTTCAACAAA[C/T]GCTACTGGGAAAACT | 22937 |
rs144764229 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47437350 | AGGCTGAGGCAGGAA[A/G]ATCACTTGAACCGGT | 22937 |
rs144801018 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SCAP | GRCh38.p7 | 3:47416453 | CTAAAAATGCAACCA[A/G]GATACCCCAAAGGCT | 22937 |
rs144849894 | snp | C/G | | | intron-variant | SCAP | GRCh38.p7 | 3:47467531 | GATCACTTGGGACCA[C/G]AGGCTTGAGGCTGCA | 22937 |
rs144927702 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SCAP | GRCh38.p7 | 3:47419064 | ACAGCCCTGGTGGCC[A/G]TGTGGGGTATCTCCC | 22937 |
rs145074102 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47415347 | GCCAGAGGGCAACTC[C/G]AAATATTAACCACCT | 22937 |
rs145164644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47461090 | TCTGTACCCCCTCCA[C/T]GCCCACCAGCTTCTA | 22937 |
rs145205087 | in-del | -/G | | | intron-variant | SCAP | GRCh38.p7 | 3:47466158 | AAAAAAAAAAAAAAA[-/G]AAAGAAATTCTCCCC | 22937 |
rs145215344 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47442550 | GGTACTAAAACGAAA[C/T]CACTACTATTGAGAA | 22937 |
rs145255240 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47431705 | CTCCTCCTCCTCACA[A/T]ATCAAGGGCACAATC | 22937 |
rs145272691 | snp | A/T | 1.98797e-05 | 0.00315269 | missense | SCAP | GRCh38.p7 | 3:47417644 | GAAAAGTTGGTGTCA[A/T]TTAAGCAGGTGAGGT | 22937 |
rs145304115 | snp | C/T | 0.000183773 | 0.00958398 | missense | SCAP | GRCh38.p7 | 3:47414335 | GGCTGCCAGTCAGTA[C/T]ATCCCACAGGCAGAT | 22937 |
rs145375232 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SCAP | GRCh38.p7 | 3:47441125 | CAGGATGGTCTCGAT[C/T]GCCTGACCTCGTGAT | 22937 |
rs145413386 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47419884 | TAACACCTGCCAACA[A/C]TTGCTGCTGGAGGGG | 22937 |
rs145416956 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SCAP | GRCh38.p7 | 3:47439197 | GCAGGTTACTTGAGG[G/T]CAGGAGTTTGACACC | 22937 |
rs145443669 | snp | A/C/G | 0.000175529 | 0.00936676 | missense | SCAP | GRCh38.p7 | 3:47418728 | CCCAGTGCCCAGCAG[A/C/G]TATGGGCCCCGGTGG | 22937 |
rs145456175 | in-del | -/TTCAT | 0.481319 | 0.0948228 | intron-variant | SCAP | GRCh38.p7 | 3:47448725 | ATTTCTGATTTTCTG[-/TTCAT]TTCAAGAGCATTCAC | 22937 |
rs145484697 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SCAP | GRCh38.p7 | 3:47464990 | GTGAACAATCTAAAA[A/G]CAAAATTAGGAAAAC | 22937 |
rs145522371 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47464031 | TTTAATATTTATTTA[C/T]TTGAGACAGAGTCTC | 22937 |
rs145723399 | snp | A/G | 0.0799831 | 0.183287 | intron-variant | SCAP | GRCh38.p7 | 3:47462610 | TACAAAAAATTAGCC[A/G]GGCGTGGTGGCACAT | 22937 |
rs145728787 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SCAP | GRCh38.p7 | 3:47461693 | ATTTCCATGACAGAG[C/T]TGATTCCCCAGCACC | 22937 |
rs145760364 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SCAP | GRCh38.p7 | 3:47443699 | TCTTGGTCCTATAGT[G/T]GTTCCTGGGAGTGCA | 22937 |
rs145765072 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | SCAP, LOC105377073 | GRCh38.p7 | 3:47477012 | TCCAGAAAGTGCAGA[A/T]CTAGTCACCAATGCA | 22937 |
rs145770545 | snp | A/G | 2.31115e-05 | 0.0033993 | missense | SCAP | GRCh38.p7 | 3:47418806 | CCCTCGGGTTCAGGC[A/G]GAGCGTGACTGGGAT | 22937 |
rs145790569 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SCAP | GRCh38.p7 | 3:47460524 | TCCCTGACTTCCCAC[A/G]ACACTTCAAGAACTG | 22937 |
rs145829837 | snp | A/G | 0.000497983 | 0.0157716 | synonymous-codon | SCAP | GRCh38.p7 | 3:47414647 | CGAGTCCTCCAGACG[A/G]AACACCTGGGACAGG | 22937 |
rs145894255 | snp | C/G | 0.00111165 | 0.0235498 | synonymous-codon | SCAP | GRCh38.p7 | 3:47414034 | CCAAAAGGAGACACA[C/G]CCCTGGCCGCCAGTC | 22937 |
rs145924826 | snp | A/T | 0.00438332 | 0.0466095 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | SCAP, LOC105377073 | GRCh38.p7 | 3:47475809 | GGTACCTGTGGTGGC[A/T]GCACCTCCCAAGCTG | 22937 |
rs146029417 | in-del | -/TAC | 0.0279526 | 0.114869 | intron-variant | SCAP | GRCh38.p7 | 3:47473116 | GACTGTGGAAGCAGG[-/TAC]TACAAGAACAGCATA | 22937 |
rs146031236 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant, missense, upstream-variant-2KB | SCAP | GRCh38.p7 | 3:47427164 | AATCTTACTTGGCAT[A/G]GTAGTGCTGGAAGAC | 22937 |
rs146168371 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | SCAP | GRCh38.p7 | 3:47430513 | GAGTTGCAAGGGATG[A/C]TGAGAGCACAGAAGG | 22937 |
rs146196919 | snp | C/T | 1.64749e-05 | 0.00287005 | intron-variant, missense, upstream-variant-2KB, utr-variant-5-prime | SCAP | GRCh38.p7 | 3:47427456 | GGCTACCTTTGAGTG[C/T]GGCTGAAGTCTGCAG | 22937 |
rs146209892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47434471 | ATATCAGTGTTCGGC[C/T]CAGAGACAGTCAACT | 22937 |
rs146306620 | snp | C/T | 4.95094e-05 | 0.00497517 | intron-variant, missense, utr-variant-5-prime | SCAP | GRCh38.p7 | 3:47428637 | AGGACTTCACAAATA[C/T]CTGCTGGACATAAGC | 22937 |
rs146330296 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SCAP | GRCh38.p7 | 3:47459576 | CCGTGATACCCACCC[A/G]AGCTGCAAAACCAGC | 22937 |
rs146367862 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | SCAP | GRCh38.p7 | 3:47431756 | GCTGCTTTAACCCCA[A/C]TCACTTACTGTAGGA | 22937 |
rs146394177 | snp | A/G | 0.000153988 | 0.00877328 | missense | SCAP | GRCh38.p7 | 3:47415163 | TCAAGGGAACCGTTG[A/G]GCCGTGCAGCCACAA | 22937 |
rs146477592 | in-del | -/AA | 0.0182019 | 0.0936463 | intron-variant | SCAP | GRCh38.p7 | 3:47422314 | ATCTGCTTGCCAGGC[-/AA]AGAGGTCCCACCTCA | 22937 |
rs146478019 | snp | C/G/T | 6.60801e-05 | 0.00574772 | downstream-variant-500B, missense | PTPN23, SCAP | GRCh38.p7 | 3:47413912 | AGCTCACTGCCAAAG[C/G/T]TGCAGACAATGGCAG | 22937 |
rs146631919 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SCAP | GRCh38.p7 | 3:47456041 | AGAAAGATTAATTGC[A/G]CAACAAAAGGTGTTG | 22937 |
rs146740960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47472141 | AAAAAATAATAATAA[C/T]AATTAAATGGGGCCG | 22937 |
rs146752387 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | SCAP, LOC105377073 | GRCh38.p7 | 3:47476726 | TGTTACAGGGCCTCA[C/T]AGAAGGGGAAGGGGA | 22937 |
rs146763622 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SCAP | GRCh38.p7 | 3:47424517 | GTGTGTGGAGAAGAA[C/T]GACTGTTCCTACACA | 22937 |
rs146871250 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SCAP | GRCh38.p7 | 3:47443419 | TGCCTGTGTAACAGA[C/T]GTCACCTTCAGCTGC | 22937 |
rs146882666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47449995 | TTCTTTGCCTTCAAA[A/G]AAACTTTTTTTTCTT | 22937 |
rs146911843 | snp | A/G | 0.0111196 | 0.0737302 | upstream-variant-2KB, intron-variant | SCAP, LOC105377073 | GRCh38.p7 | 3:47477590 | AAAAAAAGAAAAAAA[A/G]AAAGAAAGAAAGAAT | 22937 |
rs146922451 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SCAP | GRCh38.p7 | 3:47453252 | TTCCTAAAATAAAGA[C/T]CTGCTTATGGCCAGG | 22937 |
rs146932538 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SCAP | GRCh38.p7 | 3:47457635 | TCTCTGGGCCGGGCA[C/T]GGTGGCTCACGTCTA | 22937 |
rs146973942 | in-del | -/GTT | 0.0138799 | 0.0821421 | intron-variant, utr-variant-3-prime, downstream-variant-500B | PTPN23, SCAP | GRCh38.p7 | 3:47413726 | TGGTTTTTTAAAAAA[-/GTT]GTTTAATATTATTAC | 22937 |
rs147006390 | snp | C/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47437273 | GGAGAAACCCTGTCT[C/T]TACTAAAAATTCAAA | 22937 |
rs147061101 | snp | C/T | 0.0178098 | 0.0926698 | upstream-variant-2KB, intron-variant | SCAP, LOC105377073 | GRCh38.p7 | 3:47477296 | GGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 22937 |
rs147170058 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | SCAP | GRCh38.p7 | 3:47464204 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 22937 |
rs147189412 | snp | A/T | 1.65266e-05 | 0.00287455 | missense | SCAP | GRCh38.p7 | 3:47419399 | CAATTTCCTCCAAAG[A/T]TCCTCATCCTCAGGC | 22937 |
rs147205087 | snp | A/G | 0.000279037 | 0.0118085 | synonymous-codon | SCAP | GRCh38.p7 | 3:47418216 | GGCAGCAGCTCACCA[A/G]CAGCATGCCGTCGCT | 22937 |
rs147215799 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | SCAP | GRCh38.p7 | 3:47454194 | AACACAGTGAAACCC[C/T]GTCTCTACTAAAAAT | 22937 |
rs147281523 | in-del | -/AG | | | intron-variant | SCAP | GRCh38.p7 | 3:47421480 | GCCCCGGAACAATGA[-/AG]AGAGAGAGAGAGGGA | 22937 |
rs147286381 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SCAP | GRCh38.p7 | 3:47468998 | GGAAATGGATAGTGA[C/T]GATGGTTGCATAACA | 22937 |
rs147323144 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SCAP | GRCh38.p7 | 3:47416300 | GACTCCCCAAGGAGT[A/G]TGCATGCAGACGGAG | 22937 |
rs147323191 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant, upstream-variant-2KB | SCAP, LOC105377073 | GRCh38.p7 | 3:47474658 | AAAAATTAGCCGGGC[A/G]TGGTGGCACACACCT | 22937 |
rs147333059 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47421682 | TAACGTCCCAAGACT[C/G]TACCCTATCCTGCAG | 22937 |
rs147439135 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SCAP | GRCh38.p7 | 3:47446764 | TGGACACTGTGAGAC[C/T]GTGTCTTTACAAAAA | 22937 |
rs147460186 | in-del | -/GGAAAGA | 0.0197687 | 0.0974348 | intron-variant | SCAP | GRCh38.p7 | 3:47421784 | CCTGCCAGCCCTGGG[-/GGAAAGA]CGGGCGAGAAAAGAT | 22937 |
rs147499233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47422745 | AGCTGCTACGGGGAA[C/T]GGGTGTTCACAGCCT | 22937 |
rs147572474 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47458282 | TCAAAAACAAAAATT[A/T]GCTGGGTGTGGTGGC | 22937 |
rs147582209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47461421 | CTGTGGACTGTGATA[C/T]GCACTGGGACCACAC | 22937 |
rs147677773 | snp | C/T | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | SCAP, LOC105377073 | GRCh38.p7 | 3:47477374 | CCATCCTGGCTAACA[C/T]GGTGGAACCCCATCT | 22937 |
rs147793503 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime, downstream-variant-500B | PTPN23, SCAP | GRCh38.p7 | 3:47413756 | CAGTCAGGAGGCAGC[A/G]GCTGGAAGATACTCG | 22937 |
rs147804004 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SCAP | GRCh38.p7 | 3:47416577 | CTGGGAGGTCACCAT[A/G]TGCCATGCCCTATTC | 22937 |
rs147880140 | in-del | -/ACACACAC | | | intron-variant | SCAP | GRCh38.p7 | 3:47443234 | CCTCAATCCCAAAAT[-/ACACACAC]ACACACACACACACA | 22937 |
rs147885193 | snp | A/G/T | 9.88495e-05 | 0.00702969 | utr-variant-5-prime, missense | SCAP | GRCh38.p7 | 3:47435043 | GCTCTCCTTGTTTGC[A/G/T]GTCAGAGTCCACAGG | 22937 |
rs147899928 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SCAP | GRCh38.p7 | 3:47437945 | ACAGTTTTCCATAGC[A/G]GTTGTACAAATTTAT | 22937 |
rs148094871 | in-del | -/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47444022 | GACTGGCTCATCAAC[-/T]TTTTTTTTCCGTTTT | 22937 |
rs148107470 | snp | A/G | 0.000462435 | 0.0151988 | intron-variant, upstream-variant-2KB | SCAP | GRCh38.p7 | 3:47427132 | CAGCAGACCAGTCAA[A/G]AGCCCAGGGTACTGT | 22937 |
rs148152356 | in-del | -/G | 0.481473 | 0.0944461 | intron-variant | SCAP | GRCh38.p7 | 3:47418075 | ATACGTGGCGGCGGG[-/G]GGTGGGGTGAGGGGG | 22937 |
rs148161880 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SCAP | GRCh38.p7 | 3:47433101 | TTTGAGGCTCAAACT[A/G]TATCGTGCTTAAGTC | 22937 |
rs148204907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47445520 | AAAGTGCTGGGATTA[C/T]AGGCATGAGCCACCA | 22937 |
rs148254941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47454339 | CGCCACTGCACTCCC[A/G]TCTGGGCGAAAGAGT | 22937 |
rs148317079 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SCAP | GRCh38.p7 | 3:47473570 | ACGGGGGTGATGACA[A/C]AAACTGTATATGAAG | 22937 |
rs148325686 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47459231 | GTACTTGTAGGAGCA[C/T]AGCCAGGACCAGCCT | 22937 |
rs148360386 | snp | G/T | 1.67894e-05 | 0.00289731 | missense | SCAP | GRCh38.p7 | 3:47414900 | GTGATGGGTTTTTGG[G/T]GTGCACAGGGCACTG | 22937 |
rs148404331 | in-del | -/AGAATG | | | intron-variant | SCAP | GRCh38.p7 | 3:47438425 | AAGAGAGAAACGACT[-/AGAATG]ACAAGTGATCAGAAT | 22937 |
rs148420487 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SCAP, LOC105377073 | GRCh38.p7 | 3:47475152 | CCAGAGCCCCCACAG[A/C]GACTCACTGCCCCCC | 22937 |
rs148430081 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47423037 | TCGCATGTCTAAGGC[G/T]CTGTGCTCTTACTGG | 22937 |
rs148460850 | snp | A/G/T | 9.45911e-05 | 0.0068766 | synonymous-codon, missense | SCAP | GRCh38.p7 | 3:47417312 | TGCCCACCTCCAGCC[A/G/T]GCCGCTGCTCCGCCC | 22937 |
rs148586029 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SCAP | GRCh38.p7 | 3:47416099 | CTAAGGGCAAGGGAC[A/G]CCCCCTCCCCAAGGA | 22937 |
rs148681312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47436872 | AACAGCATACCACTC[C/T]CCACCACCAAAGGTA | 22937 |
rs148724099 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SCAP | GRCh38.p7 | 3:47449199 | TAGGGTCAGATGCAC[A/G]TATGTTAGTTCTGAG | 22937 |
rs148754419 | snp | A/T | 1.66452e-05 | 0.00288484 | missense | SCAP | GRCh38.p7 | 3:47414263 | TGCTGATGACACAGG[A/T]GGTGGTACAGGTAAG | 22937 |
rs148778273 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47457458 | ACTGAATCACCTTGT[A/G]TTCCCTAGAGCACCC | 22937 |
rs148798865 | snp | A/C/G/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47463177 | CCTGTTTATTCCTCC[A/C/G/T]GCGGAAAGTTTAGGA | 22937 |
rs148821230 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SCAP | GRCh38.p7 | 3:47465495 | CAGCTGGCCAGGCAC[A/G]GTGGCCCATGCCTGT | 22937 |
rs148830361 | snp | C/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47452987 | TGTAGTCCTGGCTAC[C/T]TGGAAGCCTGAGTGG | 22937 |
rs148831145 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime, downstream-variant-500B | PTPN23, SCAP | GRCh38.p7 | 3:47413770 | CGGCTGGAAGATACT[C/T]GGCTCTTTCCCCCAA | 22937 |
rs148862651 | snp | C/T | 3.36836e-05 | 0.00410374 | missense | SCAP | GRCh38.p7 | 3:47414883 | CAGCGGCTTTCAGGG[C/T]TGTGATGGGTTTTTG | 22937 |
rs148875000 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | SCAP | GRCh38.p7 | 3:47472881 | AGATCGGGAGTCTGA[C/G]ACCAGCCTGACCAAT | 22937 |
rs148914389 | snp | A/G | 0.000153988 | 0.00877328 | missense | SCAP | GRCh38.p7 | 3:47413987 | TTCTTCCCCAGGTAG[A/G]CTGTCTGTAACAGGT | 22937 |
rs148942396 | snp | C/T | 0.00478085 | 0.0486577 | upstream-variant-2KB, intron-variant | SCAP, LOC105377073 | GRCh38.p7 | 3:47477284 | AAAGTATTCGCTGGG[C/T]GCGGTGGCTCACGCC | 22937 |
rs148982972 | snp | A/C/T | 0.000642496 | 0.0179131 | missense | SCAP | GRCh38.p7 | 3:47418149 | CCTGGGCGCGGAATG[A/C/T]GCGTTAGGCAATCCC | 22937 |
rs149003080 | snp | A/G | 1.66021e-05 | 0.0028811 | missense, intron-variant, upstream-variant-2KB | SCAP | GRCh38.p7 | 3:47425997 | CTGCCATGAACCTAC[A/G]CGTGGAGAAGTAGAT | 22937 |
rs149033051 | snp | A/G | 0.0163266 | 0.0888637 | synonymous-codon | SCAP | GRCh38.p7 | 3:47418402 | GCAGGGCAGCTCCCC[A/G]CGCCTCCGCCGCCCG | 22937 |
rs149082564 | snp | A/C/G/T | 0.00850346 | 0.0646517 | missense, intron-variant, upstream-variant-2KB | SCAP | GRCh38.p7 | 3:47426107 | ACCAGGCTCTCCGCC[A/C/G/T]GAAGGCTGCAGTTGG | 22937 |
rs149172776 | in-del | -/TG/TGTG | 0.00716266 | 0.059414 | intron-variant | SCAP | GRCh38.p7 | 3:47448355 | CAGAGTCTTTCTGCA[-/TG/TGTG]TGTGTGTGTGTGTGT | 22937 |
rs149205262 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SCAP | GRCh38.p7 | 3:47440039 | AGTACTGCTCTGTAC[C/T]TTCCCTGGGGTGACC | 22937 |
rs149281537 | in-del | -/ATATATATATAT | | | intron-variant | SCAP | GRCh38.p7 | 3:47455063 | ATACAAAAAAATTAC[-/ATATATATATAT]ATATATATATATATA | 22937 |
rs149336840 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | SCAP | GRCh38.p7 | 3:47442236 | GGGTCATCAGATGTC[A/C]TCTCATATCAAACTC | 22937 |
rs149344058 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SCAP | GRCh38.p7 | 3:47467205 | ATATATCTAACAAGG[A/G]TTTAATATCCAGAAT | 22937 |
rs149354257 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SCAP | GRCh38.p7 | 3:47415586 | GTGTTGCGGAAGCCT[G/T]CATTCTCCACATAAA | 22937 |
rs149398103 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | SCAP, LOC105377073 | GRCh38.p7 | 3:47474850 | GAGGAACACCTAAAA[C/T]GGATACAGCACTAAC | 22937 |
rs149558460 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47421574 | ATTTTCTGAGATGTC[A/G]GTGTTGAGACCTCTA | 22937 |
rs149573868 | snp | A/C/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47431272 | CCACAATCCCTACTT[A/C/T]ACAGCACAAAGACTG | 22937 |
rs149611411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47429659 | TAGAGATGGGGTCTC[A/G]CTATGTTGCCCAGGC | 22937 |
rs149667104 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47464449 | CCCAAAGTGCAAGGA[C/T]GGTTTAACAAAAATC | 22937 |
rs149711392 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47431600 | TCAGGCATTTTGTAG[C/G]GTGTTCCTCAACTAG | 22937 |
rs149803614 | snp | A/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47472460 | AAAAAAAATAAAATA[A/T]AATAATAATAATAAT | 22937 |
rs149824484 | snp | A/G | 1.66319e-05 | 0.00288369 | synonymous-codon, utr-variant-5-prime | SCAP | GRCh38.p7 | 3:47422526 | GATGGACCAGCTCTC[A/G]CTGCTTAGGCCTGCA | 22937 |
rs149870945 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SCAP | GRCh38.p7 | 3:47470588 | AGAACCTTTGCGGGG[C/T]GCAGTGGCTCACGCC | 22937 |
rs149876928 | snp | A/T | 0.000643357 | 0.0179239 | missense | SCAP | GRCh38.p7 | 3:47419479 | CTCCACGCTCAGGTG[A/T]CTCGCCTGGCGACGT | 22937 |
rs149921326 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | SCAP, LOC105377073 | GRCh38.p7 | 3:47476920 | CTGCCCGAGACACCC[A/G]CACCCACCCCAGGGC | 22937 |
rs150019606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47448960 | CTTGTTTAAGTCCCA[C/T]GTAAAATTTTGAATT | 22937 |
rs150123549 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47452563 | TCATCCATCCTGTTC[C/T]TCACAAATGTCCCAA | 22937 |
rs150141381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47414761 | CCAGCCTCTCCCTGA[C/T]GAATGCATCAGGCTC | 22937 |
rs150166851 | in-del | -/GCCCC | 0.0678144 | 0.171197 | intron-variant, utr-variant-3-prime, downstream-variant-500B | PTPN23, SCAP | GRCh38.p7 | 3:47413804 | AGGTTCAGTGCATTG[-/GCCCC]GCCCCCACACAGCAC | 22937 |
rs150182753 | snp | A/G | | | intron-variant | SCAP | GRCh38.p7 | 3:47437445 | AAAAAAAAAAAAAAA[A/G]GGAGAATAAAGTTGG | 22937 |
rs150219185 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | SCAP | GRCh38.p7 | 3:47466886 | CTCAGAAGTTTGAGA[A/C]CAGCCTGGACAACAT | 22937 |
rs150236966 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | SCAP | GRCh38.p7 | 3:47433534 | AACTCTCCTAGTCAG[C/G]AAACACAAATATTCC | 22937 |
rs150328328 | snp | C/T | 7.36567e-05 | 0.00606819 | missense | SCAP | GRCh38.p7 | 3:47417804 | CAAGCCCGCTGCCCA[C/T]GCCACTGTCCCGGCG | 22937 |
rs150345243 | snp | C/G | 0.000153988 | 0.00877328 | missense, intron-variant, upstream-variant-2KB | SCAP | GRCh38.p7 | 3:47426129 | TGCAGTTGGGGCTGG[C/G]GTGCAGAAGCATCAG | 22937 |
rs150375439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47461890 | AATACAAAAATTAGC[C/T]GAGCATGGTGACAGG | 22937 |
rs150395715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47439005 | CATACATGATATTTA[A/G]TATGTGCCAGGCACT | 22937 |
rs150397046 | snp | A/G | 0.000633713 | 0.0177892 | missense | SCAP | GRCh38.p7 | 3:47420702 | TGCCGCTCGTAGCGC[A/G]TTGGCTGTCCCACTG | 22937 |
rs150427686 | snp | A/C/T | 0.0023933 | 0.0345097 | intron-variant | SCAP | GRCh38.p7 | 3:47421205 | AGCAGCAGCTCACCC[A/C/T]GTCTCCACCAGGGGG | 22937 |
rs150498643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47441526 | TAAAGGAAAAAAAAA[C/T]CCAAGAGCTGAGTTC | 22937 |
rs150534361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47423744 | AAGTACAGTCCAATG[A/G]CCCCATGGCTCCCCA | 22937 |
rs150646187 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SCAP | GRCh38.p7 | 3:47454688 | AGGAGGCAGAAGTTA[C/T]AGTGAGCCAAGATTG | 22937 |
rs150650567 | snp | A/G | | | intron-variant, upstream-variant-2KB | SCAP | GRCh38.p7 | 3:47426400 | TTTGTCTCCCTTTCC[A/G]GACCTACTCCAACAC | 22937 |
rs150698843 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SCAP | GRCh38.p7 | 3:47460119 | CAGTCAGACCTTATG[A/G]TTGTCTTCCCTTGTT | 22937 |
rs150740890 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SCAP | GRCh38.p7 | 3:47469957 | TTGTGAAGAGAGAAG[C/T]GGTTTTGAAAGAAAT | 22937 |
rs150799323 | snp | C/T | 0.000148514 | 0.00861596 | missense | SCAP | GRCh38.p7 | 3:47419469 | TCTGCTGGACCTCCA[C/T]GCTCAGGTGACTCGC | 22937 |
rs150899835 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SCAP | GRCh38.p7 | 3:47463430 | AGTGGGCCGGGGTGC[A/G]GTGGCTCGTGCCTGT | 22937 |
rs151005886 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SCAP | GRCh38.p7 | 3:47431485 | CCATCCAGGAAACCA[C/T]GTTACGTTTAGCTGT | 22937 |
rs151014440 | snp | C/T | 0.00904226 | 0.0666286 | synonymous-codon | SCAP | GRCh38.p7 | 3:47414198 | CTGAATGGAGTAGAA[C/T]TTGATGCCTGTGCTG | 22937 |
rs151151424 | snp | A/G | 0.00150062 | 0.0273507 | missense | SCAP | GRCh38.p7 | 3:47417705 | GAGGGCCCCGGGGGC[A/G]GTGTCTCAGGGGAGG | 22937 |
rs151173991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47457508 | AGCAGAAAGTCACTA[C/T]AGGTCTGCTCACTGA | 22937 |
rs151202256 | snp | C/G | 0.000116843 | 0.0076425 | missense | SCAP | GRCh38.p7 | 3:47414317 | CAAACACATGGCTGA[C/G]CCGGCTGCCAGTCAG | 22937 |
rs180680768 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | SCAP, LOC105377073 | GRCh38.p7 | 3:47477747 | GGACTACAGATGAGC[A/G]CCACCATGCCATTTT | 22937 |
rs181030373 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47415383 | CTCAGTTTCTTCATC[C/T]GTAAAATGGGGATAA | 22937 |
rs181042654 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SCAP | GRCh38.p7 | 3:47426639 | AGACGGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 22937 |
rs181074944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47437029 | ATTCTCCACACTGGC[A/G]CACATAGCAGATCAT | 22937 |
rs181075151 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SCAP | GRCh38.p7 | 3:47458159 | AGGGCGTGGCCAGGC[A/G]CAGTGGCTCATGCCT | 22937 |
rs181105120 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SCAP | GRCh38.p7 | 3:47427007 | AGACAGCATCATCTA[C/G]TCTGAGGGATGTAAA | 22937 |
rs181132564 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SCAP | GRCh38.p7 | 3:47467890 | CTCCCCCCATCCCCC[A/G]GCAGGCCCTGGTGAG | 22937 |
rs181139159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47448833 | CATCTGTGTCATGTT[A/G]TGGTTGCCATCTGTT | 22937 |
rs181191240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47457962 | AAAATTAGCCAGTAA[C/T]CTGGGAGAATTTTCA | 22937 |
rs181203105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47436408 | AGAGGCCAAGCGGGC[A/G]GATCATTTGAGCTCA | 22937 |
rs181203478 | snp | A/G | 0.0150606 | 0.0854603 | upstream-variant-2KB, intron-variant | SCAP, LOC105377073 | GRCh38.p7 | 3:47477478 | CGGGAGGCTGAAGCA[A/G]GAGAATGGCATGAAC | 22937 |
rs181299723 | snp | C/G | | | intron-variant | SCAP | GRCh38.p7 | 3:47442076 | ACTGAACAGGGAGTT[C/G]CCTCCTGACTTCTCA | 22937 |
rs181309010 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47421426 | GCTAGAGCCCAGGCC[C/T]GATTCAGGGGCTCTC | 22937 |
rs181310417 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47461468 | CACAGTCACTTCTCA[G/T]ACTGGAACTTGCTTG | 22937 |
rs181324707 | snp | A/G | | | intron-variant | SCAP | GRCh38.p7 | 3:47454286 | GCAGGAGAATGGTGT[A/G]AACCCCGGGGGACGG | 22937 |
rs181449719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47432541 | CATCCCACACCACGC[A/G]TATGCAATAAACGAG | 22937 |
rs181459835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47471827 | TATGTACTACAGTGA[C/T]AATACAGTGTACATT | 22937 |
rs181666655 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47432111 | ATCACAAGATCAGGA[C/G]ATCAAGACCATCCTG | 22937 |
rs181690875 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47452846 | TAATCCCAGCAGTTT[C/G]GGACACTGAGGCAGG | 22937 |
rs181712898 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | SCAP | GRCh38.p7 | 3:47444156 | AATAGAAAACTCTAG[G/T]AGGCCCAGGGATCTA | 22937 |
rs181716915 | snp | G/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47471258 | AAAAATAAAATAAAA[G/T]AAGAATAAGAACAAA | 22937 |
rs181718311 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SCAP | GRCh38.p7 | 3:47422654 | CCCAGCCCTTTGAAG[G/T]AGCCATTCCACCAAA | 22937 |
rs181880107 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47472581 | TTTGGACCCCACTGC[A/G]AAGCTTCCTTATGAT | 22937 |
rs181897229 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | SCAP | GRCh38.p7 | 3:47426752 | CCAACACTCTTGATT[A/G]CCAGAGGCCTAGGAG | 22937 |
rs181905406 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SCAP | GRCh38.p7 | 3:47448246 | TTTTAGCAACTATGT[C/T]TTCAATTTTGATTTT | 22937 |
rs181984169 | snp | A/C | 0.00795532 | 0.062565 | upstream-variant-2KB, intron-variant | SCAP, LOC105377073 | GRCh38.p7 | 3:47478420 | TGGTAAATCTGCTAC[A/C]GAATGCCCCCCATGG | 22937 |
rs182018344 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SCAP | GRCh38.p7 | 3:47442546 | ACCAGGTACTAAAAC[A/G]AAACCACTACTATTG | 22937 |
rs182040750 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SCAP | GRCh38.p7 | 3:47419071 | TGGTGGCCGTGTGGG[G/T]TATCTCCCTCCCCAC | 22937 |
rs182055526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47439813 | TAGCTCACCTGCAAG[A/G]CTCAGCACTGGGTTC | 22937 |
rs182066672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47460310 | AGCATAAGAAATTAT[A/G]AAGTATTAATTTTGG | 22937 |
rs182187298 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SCAP | GRCh38.p7 | 3:47415614 | AAAAGCAGCTTCAAC[C/T]CAAGCACAGCTCACA | 22937 |
rs182187506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47458929 | TCTTGCCTCAGCCTC[A/G]CAAGTAGCTGGGATT | 22937 |
rs182299317 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SCAP | GRCh38.p7 | 3:47462192 | ACATTCATATTGTTG[G/T]GCAGCCATCACCACC | 22937 |
rs182366851 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | SCAP | GRCh38.p7 | 3:47468663 | ATTTTCTCCCACTCT[G/T]TAGGTTGCCTGTTCA | 22937 |
rs182446051 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47467328 | AAGATATACAGGCTC[A/G]GTGGGGTGGCTCATG | 22937 |
rs182460814 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SCAP | GRCh38.p7 | 3:47437361 | GGAAAATCACTTGAA[C/G]CGGTGAGCTGAGATG | 22937 |
rs182481753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47417065 | TCAAGACTCAAGAGA[A/G]TATGGCCTAGCCAAC | 22937 |
rs182574952 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47423498 | TCCCAGGCTCAAGCA[A/G]TCCTCCCACCTCAGC | 22937 |
rs182582124 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47444850 | AATCTTGGCTCAATG[A/C]AATCTCTGTCTCCTG | 22937 |
rs182608214 | snp | G/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47450067 | CAGTGGCGTGATCTC[G/T]GCTCACCGCAACCTC | 22937 |
rs182656531 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47450863 | TTATTTATTTTTCTT[G/T]TTTTAGAGATGGGGT | 22937 |
rs182668236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47469271 | AAGAATCGCTTGAAC[C/T]GGGAGGCAAAGGTTG | 22937 |
rs182755936 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47427783 | TTTGCTCTCTGGTAT[C/G/T]GCCAAAGAGCCTGAC | 22937 |
rs182877295 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SCAP | GRCh38.p7 | 3:47446421 | CATGATCTGCCCTCC[C/T]TCGCCTCCCAAAGGG | 22937 |
rs182886898 | snp | A/G | | | intron-variant | SCAP | GRCh38.p7 | 3:47473184 | CACACAACACACTCC[A/G]TCTCAAATTCGCTAG | 22937 |
rs182893288 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47465099 | AAACATTGCTGAAAC[A/C]AATTAAAGACGTAAA | 22937 |
rs183094745 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SCAP | GRCh38.p7 | 3:47456822 | CTGGAAAAATACAAC[C/T]GCAATTCATATCGCT | 22937 |
rs183237531 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SCAP | GRCh38.p7 | 3:47459874 | GTAAGCCTGAGGGTA[C/T]TGCAGGAGACCAGGG | 22937 |
rs183247112 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47433783 | TGAGGCAGGAGAATC[A/G]CTTTCAACCCAGGAG | 22937 |
rs183250386 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SCAP | GRCh38.p7 | 3:47429282 | AGCCTCTTTTGCTCA[A/G]TAACACATCTACTAT | 22937 |
rs183321423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47433293 | TGACCACTGAGCTGT[A/G]TGACACCAGGTGACT | 22937 |
rs183325656 | snp | A/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47455194 | CAACAACAAGCAGGC[A/T]GAAGTAAAATAATGA | 22937 |
rs183347759 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47435195 | GGCAGTCCTCTCTCA[A/G]CACTGACACAGGAGC | 22937 |
rs183372625 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | SCAP | GRCh38.p7 | 3:47474146 | GGCGGGCGCCTGTAG[C/T]CCCAGCTACTTGGGA | 22937 |
rs183456922 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | SCAP | GRCh38.p7 | 3:47450143 | GCTGGAGTTACAGGC[A/G]TGCGCCACCCCACCC | 22937 |
rs183472881 | snp | A/C | 1.64798e-05 | 0.00287047 | intron-variant, missense, utr-variant-5-prime | SCAP | GRCh38.p7 | 3:47428559 | CCACCAGTTGGAATG[A/C]CCGGGACAAAGGTGA | 22937 |
rs183474418 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47468921 | AGGAAGGGATCCAGT[C/T]TCAGCTTTCTACATA | 22937 |
rs183479712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47456146 | AGTGGCTCAGGCCTA[C/T]AATCCCAGCACTTTG | 22937 |
rs183651728 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47442482 | GTTGTCCAAGATACT[C/G]TTCTAATGGACTTTG | 22937 |
rs183668990 | snp | A/G | | | intron-variant | SCAP | GRCh38.p7 | 3:47421671 | TGTCTCAGCTCTAAC[A/G]TCCCAAGACTGTACC | 22937 |
rs183670424 | snp | C/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47461804 | TCTCGGAGGCCGAGG[C/T]AAACAGATCACTTCA | 22937 |
rs183822995 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SCAP | GRCh38.p7 | 3:47446032 | AGATGCGCGCCACCA[C/T]GCCCAGCTAATTTTT | 22937 |
rs183988902 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | SCAP | GRCh38.p7 | 3:47424179 | GGTGCTGGGCAGAAA[A/C]CCTCCCTTGTCCACC | 22937 |
rs184024978 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47464584 | AAAAAATACTCAATG[A/G]AATAGGAATAGAAGG | 22937 |
rs184131789 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47430385 | GTAACAGGCATGTCG[C/T]GGAGCACCCCAAAAC | 22937 |
rs184139041 | snp | C/T | 4.96241e-05 | 0.00498092 | intron-variant | SCAP | GRCh38.p7 | 3:47420901 | CCAGGGCTGAGGAGG[C/T]GGGCAGGGCAGGGCT | 22937 |
rs184152172 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SCAP | GRCh38.p7 | 3:47441969 | CACCTCAGCCTCCCA[A/G]TGTTGGAATTACAGG | 22937 |
rs184165230 | snp | A/G | | | intron-variant | SCAP | GRCh38.p7 | 3:47470271 | AGGCTCAGGTAAGAA[A/G]ATTACTGCATCTGCT | 22937 |
rs184277376 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47466345 | AAAACAATAGAGAGC[C/T]CAGATCTTCTGTAGT | 22937 |
rs184283350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47447269 | AGCTGGGTGTGGTGG[C/T]ACACACTTGTAATCC | 22937 |
rs184287078 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SCAP | GRCh38.p7 | 3:47451827 | AAAGCCCAAATGCCT[C/T]CCCCTAGCTCTCAGG | 22937 |
rs184298880 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SCAP | GRCh38.p7 | 3:47436413 | CCAAGCGGGCGGATC[A/G]TTTGAGCTCAGGAGT | 22937 |
rs184379578 | snp | C/G | 6.81118e-05 | 0.00583534 | intron-variant, upstream-variant-2KB | SCAP | GRCh38.p7 | 3:47425650 | AGGGCGGCCCCTCCC[C/G]CAGCCCCCGGCCCAC | 22937 |
rs184488392 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | SCAP | GRCh38.p7 | 3:47466963 | CCAGGCATGGTGGTG[A/T]GCACCTGTAGTTTCA | 22937 |
rs184666237 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47435541 | AGGCGCCTGCCACTA[C/T]ATCCAGGTAATTTTT | 22937 |
rs184691942 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SCAP | GRCh38.p7 | 3:47457188 | GTGGCAGCACCAGCA[A/G]CCTCTGGGGAGAGGA | 22937 |
rs184706186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SCAP, LOC105377073 | GRCh38.p7 | 3:47474844 | ATCACTGAGGAACAC[C/T]TAAAATGGATACAGC | 22937 |
rs184795523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47430930 | ACAGCATAGGCAAGG[A/G]CCAAGATGCTGACCA | 22937 |
rs184811646 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47470997 | GGATTAAAGGATATA[C/G]ATGAAACAAGAGTGT | 22937 |
rs184819786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47452379 | CAAACCACTTGTTGA[A/G]TAAGTGATGAACAAA | 22937 |
rs184879979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47461148 | CCCTAAGACTCCCTC[C/T]ACACTCTTCAAGGCA | 22937 |
rs184893252 | snp | C/T | 0.000354073 | 0.0133008 | intron-variant, upstream-variant-2KB | SCAP | GRCh38.p7 | 3:47426197 | CAGGGTGGGGGTAAA[C/T]GGAAGTGTTGCTCTT | 22937 |
rs184924136 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SCAP | GRCh38.p7 | 3:47458116 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 22937 |
rs184981755 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SCAP | GRCh38.p7 | 3:47464258 | TGATCTCAGGTGATC[C/T]GCCTGCCTCGGCCTC | 22937 |
rs185010746 | snp | C/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47435688 | ACCGTGCCTGGCTAG[C/T]TTATACATTTAATGA | 22937 |
rs185021684 | snp | C/G | 0.031825 | 0.122064 | upstream-variant-2KB, intron-variant | SCAP, LOC105377073 | GRCh38.p7 | 3:47477560 | TGGGCGACAGAGCGA[C/G]ACTCCGTCTCAAAAA | 22937 |
rs185043601 | snp | A/C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SCAP, LOC105377073 | GRCh38.p7 | 3:47476385 | AGGATCACCTGAGCC[A/C/T]GGGAGGTCGAGGCCA | 22937 |
rs185111411 | snp | A/C | 0.0023933 | 0.0345097 | downstream-variant-500B | PTPN23, SCAP | GRCh38.p7 | 3:47413663 | AGTGTGTGCACAAAC[A/C]ATTCCAAGAGACACA | 22937 |
rs185135903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47457592 | TGAAAGTTGTCAAGC[A/G]GACCAATGCTAAGGG | 22937 |
rs185332987 | snp | C/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47458203 | TTTGGGAGGCCAAGG[C/T]GGGTGGATCACGAGG | 22937 |
rs185335030 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SCAP | GRCh38.p7 | 3:47437295 | AAATTCAAAATTAGC[C/T]GGGCGTGGTGGCGTA | 22937 |
rs185349854 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SCAP, LOC105377073 | GRCh38.p7 | 3:47478337 | ATGGCAAACAATCCT[C/T]CACTGCCCTAAGAGA | 22937 |
rs185548472 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SCAP | GRCh38.p7 | 3:47447960 | CAGTAAGCTGAGATA[C/G]TGCCACTGCACTCCA | 22937 |
rs185633157 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SCAP | GRCh38.p7 | 3:47420164 | CCAAGGCCAGCCCAG[C/T]CCGGCTGGTGAATGA | 22937 |
rs185641483 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SCAP | GRCh38.p7 | 3:47467991 | TTTCTGTCCTTGCGA[C/T]AGTTTGCTCAGAATG | 22937 |
rs185655708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47460564 | TTTTTGTTGTTGTTG[C/T]CTTTTTGAGACAGAG | 22937 |
rs185684893 | snp | C/T | | | intron-variant, upstream-variant-2KB | SCAP | GRCh38.p7 | 3:47426665 | GATGGTCTCGATCTC[C/T]TGACCTCATGATCCG | 22937 |
rs185720129 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SCAP | GRCh38.p7 | 3:47426813 | CCAATTGGGGAGCTG[C/T]CTGCAGTGCCCCACT | 22937 |
rs185732125 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SCAP | GRCh38.p7 | 3:47448392 | TTTGGAAATTTCTAC[A/G]TAGACTTATCATGTT | 22937 |
rs185748709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47467522 | AGGTGGGAGGATCAC[C/T]TGGGACCAGAGGCTT | 22937 |
rs185796500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47441121 | TGGCCAGGATGGTCT[C/T]GATCGCCTGACCTCG | 22937 |
rs185806499 | snp | C/T | 3.30295e-05 | 0.0040637 | missense | SCAP | GRCh38.p7 | 3:47413951 | AGCACCAGGATCTGG[C/T]GGGCAGGCTGGGCCT | 22937 |
rs185845568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47432942 | GGACAGGCAGGTAAC[C/T]CTATTCATAGCCAAC | 22937 |
rs185847531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47471830 | GTACTACAGTGATAA[C/T]ACAGTGTACATTATA | 22937 |
rs185868518 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SCAP | GRCh38.p7 | 3:47423151 | ATGAATGGACGGCTG[C/T]CTACAGCCCCATTCC | 22937 |
rs185882890 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | SCAP | GRCh38.p7 | 3:47444157 | ATAGAAAACTCTAGG[A/C]GGCCCAGGGATCTAG | 22937 |
rs185891303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47471497 | TAGTTCTAGTATACT[C/T]AGAGGTATACTACAG | 22937 |
rs185901719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47463199 | AGTTTAGGAAACATC[C/T]TACAACAAGCCCACA | 22937 |
rs185961089 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47454781 | ACACATATATATATA[A/T]AAAATAAATACAGAC | 22937 |
rs185983388 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SCAP | GRCh38.p7 | 3:47450083 | GCTCACCGCAACCTC[C/T]GCCTCCTGGGCTCAA | 22937 |
rs186122784 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47427893 | AAGCCCAAAAGCCCA[G/T]CAGCTCTGAGGACGG | 22937 |
rs186130932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47468687 | CTGTTCAGTCTGATG[A/G]TAGTTTCTTTTGCTG | 22937 |
rs186492446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SCAP | GRCh38.p7 | 3:47427322 | CTGCAGAGCCACCAA[A/G]GACCCCTTTCTCACC | 22937 |
rs186530575 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SCAP | GRCh38.p7 | 3:47432241 | GGAATCACTTGAACC[C/T]GGGAGGCGGAGGTTC | 22937 |
rs186566215 | snp | A/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47472716 | ATCCCCACACTAGAG[A/T]CAGTGACGCTGGCTT | 22937 |
rs186569379 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47433334 | CATCTCCTTCTCAAT[A/C]CTGCAGGGGATGAGC | 22937 |
rs186570746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47455446 | CTAAAAATACAAAAA[C/T]TAGCTGGGCATTGTG | 22937 |
rs186574937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47435368 | GCCCAACTGGTAAAA[C/T]AGACTGTTCTGTTAA | 22937 |
rs186580151 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SCAP | GRCh38.p7 | 3:47445492 | ACCAGGTGATCCACC[A/G]CCTCGGCCTCCCAAA | 22937 |
rs186646772 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SCAP | GRCh38.p7 | 3:47437379 | GTGAGCTGAGATGGC[A/G]CCACTGCACTCTAGC | 22937 |
rs186650182 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | SCAP, LOC105377073 | GRCh38.p7 | 3:47478917 | AGCTGGGACTACAGG[C/G]TTGCGCCATCGCGCC | 22937 |
rs186688564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47440136 | AGGGAAATTAAGTGC[A/G]GCAGTCCTTTGGGTT | 22937 |
rs186698810 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47460326 | AAGTATTAATTTTGG[A/G]AACTGATAAATGTCC | 22937 |
rs186722537 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SCAP | GRCh38.p7 | 3:47448931 | TTTGAATATTATGCT[A/G]TGTGACTCTAGCTCT | 22937 |
rs186761625 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SCAP | GRCh38.p7 | 3:47452854 | GCAGTTTGGGACACT[A/G]AGGCAGGAAGACTGC | 22937 |
rs186858967 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47459480 | CCGTAAGTGTCGGCC[A/G]GCTGAGAAATAAAGA | 22937 |
rs186860557 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47415868 | TTGGAAGTGGGTGGA[A/C]AAGGAGAGACCACAG | 22937 |
rs187169574 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SCAP | GRCh38.p7 | 3:47439082 | GTTATGTCCTGATAA[C/T]GCTGTCGTAAATTGA | 22937 |
rs187172584 | snp | C/T | 5.01895e-05 | 0.00500921 | missense | SCAP | GRCh38.p7 | 3:47417144 | CCAAGAACACCAGAG[C/T]GGTAATGCCTGAGGA | 22937 |
rs187182640 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47459914 | GTCCTTATCTCAACC[A/G/T]CATAAGACAGACACT | 22937 |
rs187362275 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47422112 | CTGCACAGCCAGTCC[C/T]CAGCTCCTGCCATGC | 22937 |
rs187382597 | snp | A/G | 0 | 0 | intron-variant | SCAP | GRCh38.p7 | 3:47462286 | TTTAACAAGTTTACT[A/G]TATAACTTGTCAAAG | 22937 |
rs187447262 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | SCAP | GRCh38.p7 | 3:47468962 | ATCGATAGTTTCTAT[A/G]TAGAATAATGAAAAC | 22937 |
rs187450300 | snp | A/C | | | intron-variant | SCAP | GRCh38.p7 | 3:47429067 | ACTTCCCAGAAATCA[A/C]CCTTCCTTCCATCAA | 22937 |
rs187455046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47450319 | AAACTTTTCACACTA[C/T]GCCTACTGGCATTTT | 22937 |
rs187538914 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | SCAP, LOC105377073 | GRCh38.p7 | 3:47474358 | TTTCCATTTCAATTT[A/G]TGACCAAAAGAATAA | 22937 |
rs187544366 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47457397 | GCTCATTCTGACTCT[C/T]TCAGCCTCCTGGATT | 22937 |
rs187553106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47446787 | TACAAAAAAAAAAAC[A/G]TTAACAATTAGCAGG | 22937 |
rs187556606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SCAP, LOC105377073 | GRCh38.p7 | 3:47475087 | CCTAGCTCCGACTGT[C/T]GCCATACAAGGTGGA | 22937 |
rs187574771 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | SCAP | GRCh38.p7 | 3:47425813 | GAAGGGGCTGAAAGT[A/G]GGAAGAGCCCCGGCC | 22937 |
rs187575138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47465305 | CCTCCTGAGTAACTG[A/G]GATTACAGGTGTATG | 22937 |
rs187617428 | snp | A/G | 0.000181727 | 0.00953049 | synonymous-codon | SCAP | GRCh38.p7 | 3:47419516 | CTCAGGTAGCTTAGG[A/G]GCATCAGGTGGGAAG | 22937 |
rs187624780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47443586 | TTCACTCGTGAAGAA[A/G]GTCTAGCGAGGTCAG | 22937 |
rs187753748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47423811 | CACTGCATATTATGC[C/T]GGAGGCAAGAGCAAG | 22937 |
rs187796753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47469307 | AGCAGAGACCACGCC[A/G]TTGCATTCCAGCTTG | 22937 |
rs187804257 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SCAP | GRCh38.p7 | 3:47456857 | AGGTGCTAAATTCCC[A/G]CGTATATAAGCAATT | 22937 |
rs187937418 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47435574 | ATTTTTAGTGGAGAC[A/G]GGGTTTCATCATGTT | 22937 |
rs188172794 | snp | A/G | | | intron-variant | SCAP | GRCh38.p7 | 3:47430193 | TGATGAGAAGCAAGG[A/G]GAGGCTCAGGCATTG | 22937 |
rs188206975 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SCAP | GRCh38.p7 | 3:47430710 | TCTGTAAAGACTCCC[C/T]GGGAGTTGGTGACAA | 22937 |
rs188223716 | snp | A/G | 0.000199101 | 0.00997551 | intron-variant | SCAP | GRCh38.p7 | 3:47414566 | CCCCACCTGCAGGCC[A/G]CTTACCTGGTCAATG | 22937 |
rs188227899 | snp | A/C/T | 0.00478085 | 0.0486577 | intron-variant | SCAP | GRCh38.p7 | 3:47466417 | GAGTCATTCTTGAAC[A/C/T]TTGTTATGATGTCAG | 22937 |
rs188256621 | snp | A/G | | | intron-variant | SCAP | GRCh38.p7 | 3:47436558 | CATCTAACCCTGGGA[A/G]GTAGAGGCTGCAGTG | 22937 |
rs188260632 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SCAP | GRCh38.p7 | 3:47458140 | TAAAAATACAAAAAT[C/T]AGCAGGGCGTGGCCA | 22937 |
rs188309990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47441313 | CATCTCTACAAAAGA[C/T]GAAAAACAGCCAAGT | 22937 |
rs188372392 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SCAP | GRCh38.p7 | 3:47461912 | GGTGACAGGCACCTA[C/T]AATCCCAGCTACTTG | 22937 |
rs188416654 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SCAP | GRCh38.p7 | 3:47456274 | GGGCATGGTGATGCA[C/T]ACCTGTAGTCCCAGC | 22937 |
rs188458863 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47450898 | CTCTGTCACCCAGGC[A/T]GGGGTACAGTGGCAC | 22937 |
rs188484404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47441984 | GTGTTGGAATTACAG[A/G]TATGAGCACTGCACC | 22937 |
rs188494560 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47421084 | CTCACTGTCCCAGCC[C/T]AAGAGGAGCAGTACC | 22937 |
rs188501070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47461444 | GACCACACAATTCTT[C/T]CAAATGTTCACAGTC | 22937 |
rs188568722 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SCAP | GRCh38.p7 | 3:47420409 | CAGGGAGGACACAAC[A/G]GGCAACTCCCCAGAG | 22937 |
rs188708239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47434121 | TTGCCAGATATGCCT[C/T]TATTTCAGCCGCAGA | 22937 |
rs188716368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47473209 | CGCTAGGTGACCCAG[A/G]GCCAGTCAAATAACT | 22937 |
rs188873722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47431091 | TTGTCTTCTGTATCA[C/T]GCTCAGCCACTAGAA | 22937 |
rs188892792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47471257 | AAAAAATAAAATAAA[A/G]TAAGAATAAGAACAA | 22937 |
rs188899171 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47452405 | ACAAACCAACCAACC[C/T]AACCAGGATCAGATA | 22937 |
rs188936480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47424800 | TCATACGACCAGCCT[A/G]ATGGGCCAAAGTGGT | 22937 |
rs188972520 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47464595 | AATGAAATAGGAATA[C/G]AAGGCAATATCCTCA | 22937 |
rs189015774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SCAP | GRCh38.p7 | 3:47426874 | GTAGTAACCAGCTGG[A/G]GATGCCTGCCCTAGG | 22937 |
rs189035955 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47467727 | AAATTGAAATCACAA[A/T]GAGATACCAATTCCC | 22937 |
rs189047938 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47448666 | TGCTATTGAGCCCAC[A/C]CAATTAATTTTTCAT | 22937 |
rs189119290 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47447695 | CTCTGACTCAAAAAA[A/G]AAAAGAAAAGAAAAG | 22937 |
rs189136973 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | SCAP, LOC105377073 | GRCh38.p7 | 3:47477655 | TCACTCCTTTACCCA[A/G]GCTGGAGTGCAGTGG | 22937 |
rs189236330 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SCAP | GRCh38.p7 | 3:47452052 | ACTTCTACAAAAAGA[C/T]CTCCCTTGACCATAT | 22937 |
rs189237940 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | SCAP | GRCh38.p7 | 3:47446120 | ACCTCGTGATCTGAC[C/T]GCCTCAGCCTCCCAA | 22937 |
rs189265314 | snp | C/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47421743 | ACAGCCCATCTGTTC[C/T]CTGCTCACCCCCATC | 22937 |
rs189383816 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47432430 | TCTCTTTGACATACA[A/C]TATATTTACTTTAAA | 22937 |
rs189399818 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | SCAP | GRCh38.p7 | 3:47426620 | TTTTTTGTATTTTTA[A/G]TAGAGACGGGGTTTC | 22937 |
rs189416236 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47471559 | ATTTATAGTGGAGAC[A/G]GGGTTTCACACATGT | 22937 |
rs189536477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47470806 | GGCGAAGGTTGCAGT[A/G]AGCCGAGATCGCACC | 22937 |
rs189555574 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47442507 | ACTTTGCCTCGCAAC[A/T]CACAAAAAAGGCTCT | 22937 |
rs189681997 | snp | A/G | | | intron-variant | SCAP | GRCh38.p7 | 3:47453897 | CCATTCAGCCTTCAG[A/G]CACTAGATAAAATGC | 22937 |
rs189702810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47439755 | TCCCAGAGGAAAGAA[C/T]AGTCACTGCACCCAG | 22937 |
rs189710681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47418905 | TCCTCCTGCTGTGCT[C/T]GCCAGCCAGTCCTCT | 22937 |
rs189938352 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47423365 | CTAGTGTGCTGGAGT[G/T]AGGCAGTAAGAGAAA | 22937 |
rs189948290 | snp | A/G | | | intron-variant | SCAP | GRCh38.p7 | 3:47444325 | GAAAACCCAGACTCA[A/G]AGATGACTCCTCATA | 22937 |
rs189962543 | snp | C/G | | | intron-variant | SCAP | GRCh38.p7 | 3:47463269 | GATCCCCAACCTGAC[C/G]AACAATCATCATCTC | 22937 |
rs189964817 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47433214 | ACTAAAACAGTCCTT[A/C]CCACCCACTTCAGTA | 22937 |
rs190042650 | snp | A/C/G | 1.71234e-05 | 0.00292599 | intron-variant, utr-variant-3-prime, downstream-variant-500B | PTPN23, SCAP | GRCh38.p7 | 3:47413824 | CCACACAGCACCCCA[A/C/G]CCTCCTGCCTGGGCA | 22937 |
rs190066015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47457723 | CCATCCTGGCTAACA[C/T]AGTGAAACCCCGTCT | 22937 |
rs190115435 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47460022 | AGGAAAAGAATTTAG[C/T]GATATCTTCCCTACT | 22937 |
rs190218067 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47467198 | ACAAATCATATATCT[A/C]ACAAGGGTTTAATAT | 22937 |
rs190327121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47436387 | CTGTAATCCCAACAC[C/T]TTGGGAGAGGCCAAG | 22937 |
rs190329185 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | SCAP, LOC105377073 | GRCh38.p7 | 3:47477073 | GCACCAGCCCCCGAC[C/T]CACTACACATTCTTC | 22937 |
rs190450586 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SCAP | GRCh38.p7 | 3:47448227 | TTATACCTACCATTT[A/C]ACTTTTTAGCAACTA | 22937 |
rs190631560 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | SCAP | GRCh38.p7 | 3:47455641 | AGAAATCTCTGAAAC[G/T]CCGAAAGACAGAAAA | 22937 |
rs190633695 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SCAP | GRCh38.p7 | 3:47433782 | CTGAGGCAGGAGAAT[C/T]GCTTTCAACCCAGGA | 22937 |
rs190764004 | snp | C/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47450058 | GCTGGAGTGCAGTGG[C/T]GTGATCTCGGCTCAC | 22937 |
rs190878097 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47458487 | ATTTCAGTTAATGAA[A/C/T]GAAAGCTGATTTCAG | 22937 |
rs190883475 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SCAP | GRCh38.p7 | 3:47437300 | CAAAATTAGCCGGGC[A/G]TGGTGGCGTATGCCT | 22937 |
rs190887026 | snp | C/G | 3.47868e-05 | 0.0041704 | intron-variant | SCAP | GRCh38.p7 | 3:47423906 | GCCCCTCCTGCAGCC[C/G]TCTGCCCAACTCTCC | 22937 |
rs190890547 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | SCAP, LOC105377073 | GRCh38.p7 | 3:47478400 | AGCTGGGGTTTATGG[A/G]GCCCTGGTAAATCTG | 22937 |
rs190898633 | snp | C/T | 1.64914e-05 | 0.00287149 | intron-variant, missense, utr-variant-5-prime | SCAP | GRCh38.p7 | 3:47428534 | CTCAGCACGTGGTTC[C/T]GGATCTCCTCCACCA | 22937 |
rs190905638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47464395 | TTTTTTTTAAAGTAG[A/G]TATTAAACATACATC | 22937 |
rs190990044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SCAP | GRCh38.p7 | 3:47427395 | ACACATCAAAAAGAC[A/G]GTGACCAATGGGCAC | 22937 |
rs191029149 | snp | A/C | | | intron-variant | SCAP | GRCh38.p7 | 3:47468163 | TTTGCTATTGTGAAT[A/C]GTGCCGTAATAAACA | 22937 |
rs191047020 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SCAP | GRCh38.p7 | 3:47472914 | GGAGAAACCTCGCCT[C/T]TACTAAAAATACAAA | 22937 |
rs191065415 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47473273 | GTGTTATCTCACCTG[G/T]TTATTATGAAAACTA | 22937 |
rs191144389 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47472078 | GTAAACCAAGATAGC[A/T]TCAATGCACTCCAGC | 22937 |
rs191161078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47446024 | GGAATTACAGATGCG[C/T]GCCACCACGCCCAGC | 22937 |
rs191290300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47456772 | TCTGGGCAACAAAGC[A/G]AGACTCCGTCTCAAA | 22937 |
rs191431911 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | SCAP, LOC105377073 | GRCh38.p7 | 3:47474606 | TAAAGACCAGCCTGG[A/G]CAACACAGCAAGACC | 22937 |
rs191439960 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SCAP | GRCh38.p7 | 3:47457130 | AAGTCTCTGCTTATT[C/T]GTCTATAAATGCACA | 22937 |
rs191549295 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47443902 | CCTGGACTTTGACTT[C/T]TAAACACAAACAAAC | 22937 |
rs191684305 | snp | A/G | 1.65378e-05 | 0.00287552 | synonymous-codon, intron-variant, upstream-variant-2KB | SCAP | GRCh38.p7 | 3:47426013 | CGTGGAGAAGTAGAT[A/G]TAGGCAAACAAGATG | 22937 |
rs191685713 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SCAP | GRCh38.p7 | 3:47465930 | ATGAGGTCAAGAGAT[A/C]GAGACCATCTTGGCC | 22937 |
rs191704104 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | SCAP | GRCh38.p7 | 3:47459759 | ATGTTCAGCTGTGCA[A/C]GTATTGTCTTGATAA | 22937 |
rs191708975 | snp | C/G | | | intron-variant | SCAP | GRCh38.p7 | 3:47416934 | CCCGGCCACCCCTAA[C/G]GCTTTTAATTGTTAC | 22937 |
rs191811783 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SCAP | GRCh38.p7 | 3:47422628 | GGAGTGGCAGAGGCA[C/T]GGCAAGGCCCCCCAG | 22937 |
rs191827999 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47462607 | AAATACAAAAAATTA[C/G]CCGGGCGTGGTGGCA | 22937 |
rs191849187 | snp | A/G | | | intron-variant | SCAP | GRCh38.p7 | 3:47468901 | TGATTTTTGTATAAG[A/G]TGTAAGGAAGGGATC | 22937 |
rs192002756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47438580 | GCACTTTGGGAGGCC[A/G]AGGTGGGTGGGTCAC | 22937 |
rs192125533 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SCAP | GRCh38.p7 | 3:47415465 | GGTGGTACCTGGTGA[A/G]TATCACGTAAGTTTG | 22937 |
rs192137707 | snp | C/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47450094 | CCTCCGCCTCCTGGG[C/T]TCAAGCAATTCTTGT | 22937 |
rs192143308 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, intron-variant, utr-variant-5-prime | SCAP | GRCh38.p7 | 3:47425523 | GCCGAAGAGTGTGCA[A/G]AGTCCCACAGACATG | 22937 |
rs192296724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47469076 | AAATGGGCCAGGCAC[A/G]TTGGCTCACACCTGC | 22937 |
rs192300733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47429183 | CTGGACTCCGGTCTC[C/T]TAGGGAGTCAACCTT | 22937 |
rs192303742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47450465 | GAGAATAGAGGGAAA[C/T]GTTAGTAGTGGTTGC | 22937 |
rs192373233 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | SCAP | GRCh38.p7 | 3:47460455 | CATATTAAAATGAAA[A/T]CTTCACCATTTATGT | 22937 |
rs192375664 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47430740 | ACTGGAGACAAGGAA[A/T]CATGGCCCTAGACAG | 22937 |
rs192386315 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SCAP | GRCh38.p7 | 3:47452309 | TGGGACAATCCCTTG[A/T]GCCCAGGAGTTTGAT | 22937 |
rs192402146 | snp | A/C | 0.021333 | 0.101051 | intron-variant | SCAP | GRCh38.p7 | 3:47470965 | TAAACTTCTCCCCCC[A/C]AAAAAAAGTATAATG | 22937 |
rs192508247 | snp | A/G | | | intron-variant | SCAP | GRCh38.p7 | 3:47466428 | GAACCTTGTTATGAT[A/G]TCAGCACTACCCATC | 22937 |
rs192528237 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47457411 | TCTCAGCCTCCTGGA[C/T]TGACTGCGTTCCCCT | 22937 |
rs192542289 | snp | A/G | 0.00478085 | 0.0486577 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | SCAP, LOC105377073 | GRCh38.p7 | 3:47475873 | CAGGGGCGGAGCGCG[A/G]CGTGCGCGCTCTCGG | 22937 |
rs192571655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47434729 | ACAGTCCCAGCTAAT[C/T]GGGAGGCTGAGGCAG | 22937 |
rs192717122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47451536 | CCAAGTAGCTAGGAC[C/T]ATAGGCGTGCACCAC | 22937 |
rs192800046 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SCAP | GRCh38.p7 | 3:47447861 | AAAATACAAAATAGC[C/T]GGGCATGGTGGCGTG | 22937 |
rs192925022 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SCAP | GRCh38.p7 | 3:47430232 | TAGAGCTTCACACTC[C/T]AGGCAGGGTGGTGTA | 22937 |
rs192929195 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47470014 | TTCGAACAAAATATC[A/G]TTTGGCATTCTTAGG | 22937 |
rs192968892 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SCAP | GRCh38.p7 | 3:47420482 | CCACTCTAAGGCCAA[C/G]TGCAGCACCACAAGG | 22937 |
rs192989351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47460918 | AAAGAGGGGAGGAGT[C/T]TGTGAGGAGAAATGT | 22937 |
rs193045636 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SCAP | GRCh38.p7 | 3:47440765 | CTCAGAGGGCTGAGG[C/T]AGGAGAATCACTTGA | 22937 |
rs193097163 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | PTPN23, SCAP | GRCh38.p7 | 3:47413512 | TACTTAGCACCTTTT[A/G]TGGATGACAGGATGG | 22937 |
rs193098010 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | SCAP | GRCh38.p7 | 3:47446122 | CTCGTGATCTGACCG[A/C]CTCAGCCTCCCAAAG | 22937 |
rs193193624 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SCAP | GRCh38.p7 | 3:47441336 | AGCCAAGTGTGGTGG[C/T]GCACACCTGTGGTTG | 22937 |
rs193217334 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SCAP | GRCh38.p7 | 3:47420110 | GGCCTCAGCCTTCCT[C/T]CCATCTCAGTTCAGC | 22937 |
rs193256181 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SCAP | GRCh38.p7 | 3:47435665 | TGCTGAGATTACAGG[C/T]GTAAGCAACCGTGCC | 22937 |
rs193258318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47464939 | GATGCAAAATGAACA[C/T]GCAAAAATCAGTTGC | 22937 |
rs199503791 | in-del | -/AT | 0.00438332 | 0.0466095 | intron-variant | SCAP | GRCh38.p7 | 3:47465076 | AGGGAGACAAAAGAC[-/AT]AAACTGAAACATTGC | 22937 |
rs199633697 | snp | C/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47416486 | ATATTGACAAGCTAA[C/T]CAGAGAAACTGGCTT | 22937 |
rs199653270 | in-del | -/GCTCAAGT | | | intron-variant | SCAP | GRCh38.p7 | 3:47429579 | GTCTCGAACTCCTGG[-/GCTCAAGT]GATCCTCCCATTTTG | 22937 |
rs199682625 | snp | C/G/T | 1.70956e-05 | 0.00292361 | intron-variant | SCAP | GRCh38.p7 | 3:47422394 | CACAGCTGGGGAGCA[C/G/T]AGCAGTTGCTTCCAT | 22937 |
rs199703791 | snp | C/T | 1.651e-05 | 0.0028731 | utr-variant-5-prime, missense | SCAP | GRCh38.p7 | 3:47442954 | CATGGTTGTAGAAGG[C/T]CCGAGATATCTTCTC | 22937 |
rs199713450 | snp | A/G | 0.000283056 | 0.0118932 | missense | SCAP | GRCh38.p7 | 3:47419625 | AATGGGCTCTGTTCC[A/G]TCACCTGGGCAGCGA | 22937 |
rs199728489 | snp | A/G/T | 6.6143e-05 | 0.0057504 | utr-variant-5-prime, missense | SCAP | GRCh38.p7 | 3:47442972 | GAGATATCTTCTCAC[A/G/T]CAGCCTTTCAGTCAG | 22937 |
rs199738061 | snp | C/T | 4.97673e-05 | 0.00498811 | missense | SCAP | GRCh38.p7 | 3:47414582 | CTTACCTGGTCAATG[C/T]ACACGGTCGTGATGG | 22937 |
rs199740248 | in-del | -/TT | | | upstream-variant-2KB, intron-variant, nc-transcript-variant | SCAP, LOC105377073 | GRCh38.p7 | 3:47476282 | ACTTGGGCAACGTAG[-/TT]GAGACCTCCGTCTCC | 22937 |
rs199745727 | snp | C/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47462775 | AAAAAAAAAAAAAAA[C/T]AAAGAAAGAAAGGAA | 22937 |
rs199779544 | snp | C/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47441874 | GTGATGTTCATCTTT[C/T]TTTTTTTTTTTTTTT | 22937 |
rs199794833 | snp | C/T | 0.000338336 | 0.0130021 | missense | SCAP | GRCh38.p7 | 3:47418824 | GCGTGACTGGGATGA[C/T]GGGCAGCAGGCTGAT | 22937 |
rs199795130 | snp | A/G | 0.0029955 | 0.0385847 | synonymous-codon | SCAP | GRCh38.p7 | 3:47417808 | CCCGCTGCCCACGCC[A/G]CTGTCCCGGCGCTGC | 22937 |
rs199842425 | snp | A/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47438429 | AGAGAAACGACTACA[A/T]GTGATCAGAATTCAT | 22937 |
rs199867325 | snp | G/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47448729 | CTGATTTTCTGTTCA[G/T]TTCAAGAGCATTCAC | 22937 |
rs199884823 | snp | C/T | 1.70072e-05 | 0.00291605 | synonymous-codon | SCAP | GRCh38.p7 | 3:47415132 | GAGGGCAGTGTGGGT[C/T]TCCAAGGAGAAGAAA | 22937 |
rs199986589 | snp | A/G | 0.000150995 | 0.00868763 | synonymous-codon, intron-variant | SCAP | GRCh38.p7 | 3:47424045 | GTAGGGGAAAATCTC[A/G]CTGGGGACAGAGAAG | 22937 |
rs200073826 | in-del | -/AGAG | | | intron-variant | SCAP | GRCh38.p7 | 3:47438428 | AGAGAAACGACTACA[-/AGAG]AGTGATCAGAATTCA | 22937 |
rs200087732 | snp | A/C/G | 0.001036 | 0.0227363 | intron-variant, upstream-variant-2KB | SCAP | GRCh38.p7 | 3:47425623 | TTCCCTGGAGGGCAG[A/C/G]GAGGGCGTATCAGGG | 22937 |
rs200143666 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, downstream-variant-500B | PTPN23, SCAP | GRCh38.p7 | 3:47413783 | CTCGGCTCTTTCCCC[A/C]AAGTCCAGGTTCAGT | 22937 |
rs200182837 | snp | A/G | 6.59011e-05 | 0.00573988 | utr-variant-5-prime, synonymous-codon | SCAP | GRCh38.p7 | 3:47435026 | CTCAGGCTGCTCAGT[A/G]GGCTCTCCTTGTTTG | 22937 |
rs200235092 | in-del | -/CAT | 0.000492975 | 0.0156922 | utr-variant-3-prime, downstream-variant-500B, cds-indel | PTPN23, SCAP | GRCh38.p7 | 3:47413216 | CTGGTCCTTACACTA[-/CAT]CATCATCATCTCATG | 22937 |
rs200269239 | snp | C/T | 3.39524e-05 | 0.00412008 | intron-variant | SCAP | GRCh38.p7 | 3:47417113 | GGGGCTGAGGCAGGC[C/T]ACGCTCACCTTTTGT | 22937 |
rs200322305 | snp | A/C/T | 5.25733e-05 | 0.00512683 | intron-variant | SCAP | GRCh38.p7 | 3:47435159 | TGTACAAAAAGGAGA[A/C/T]AAGAATTAGACACTA | 22937 |
rs200337639 | snp | A/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47431267 | AACTCCCACAATCCC[A/T]ACTTTACAGCACAAA | 22937 |
rs200396968 | snp | G/T | 0.000165736 | 0.00910167 | intron-variant | SCAP | GRCh38.p7 | 3:47421060 | ATGGGGATGGGGGGG[G/T]GCCGTGACCTCACTG | 22937 |
rs200462184 | in-del | -/A | | | intron-variant | SCAP | GRCh38.p7 | 3:47436633 | ACCCCATCTCAAGTG[-/A]AAAAAAAAAGAAAAA | 22937 |
rs200490255 | snp | A/G/T | 6.67312e-05 | 0.00577591 | stop-gained, synonymous-codon | SCAP | GRCh38.p7 | 3:47420695 | AGCCAGCTGCCGCTC[A/G/T]TAGCGCGTTGGCTGT | 22937 |
rs200491328 | snp | C/T | 0.000164715 | 0.0090736 | intron-variant, missense, upstream-variant-2KB, utr-variant-5-prime | SCAP | GRCh38.p7 | 3:47427521 | ATGTCAGGATCAGCA[C/T]GGAAGCGTTCCCAGT | 22937 |
rs200526436 | snp | A/T | | | intron-variant, upstream-variant-2KB | SCAP, LOC105377073 | GRCh38.p7 | 3:47474263 | GAGCGAGACTCCATC[A/T]CAAAAAAAAAAAGAA | 22937 |
rs200551807 | in-del | -/A | 0.0178098 | 0.0926698 | intron-variant | SCAP | GRCh38.p7 | 3:47470865 | AGACTCTGTTTCAAG[-/A]AAAAAAACAAAAAAA | 22937 |
rs200561713 | snp | A/G | 0.000214974 | 0.0103654 | synonymous-codon | SCAP | GRCh38.p7 | 3:47414007 | CTGTAACAGGTCCCC[A/G]TAGTTTAGGTCCCAA | 22937 |
rs200597020 | snp | A/G | 6.60077e-05 | 0.00574452 | missense | SCAP | GRCh38.p7 | 3:47419470 | CTGCTGGACCTCCAC[A/G]CTCAGGTGACTCGCC | 22937 |
rs200613937 | snp | A/G | 1.68142e-05 | 0.00289945 | synonymous-codon | SCAP | GRCh38.p7 | 3:47414920 | ACAGGGCACTGTGTG[A/G]GTCAGGTGACAGGCC | 22937 |
rs200636530 | snp | A/G | 0.000146359 | 0.00855326 | missense | SCAP | GRCh38.p7 | 3:47417456 | CCTGGGACAGCACCG[A/G]CCCAGGCGAGGGTGG | 22937 |
rs200661820 | snp | C/T | 0.000399281 | 0.0141238 | missense, intron-variant, upstream-variant-2KB | SCAP | GRCh38.p7 | 3:47425603 | TGGACTTGACCATGT[C/T]GATCTTCCCTGGAGG | 22937 |
rs200729754 | in-del | -/C | 0.0150606 | 0.0854603 | intron-variant | SCAP | GRCh38.p7 | 3:47465844 | GTTTAAAAAAACAAA[-/C]AAAAAAAAAGCTGGG | 22937 |
rs200753156 | snp | C/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47466158 | AAAAAAAAAAAAAAA[C/T]AAAGAAATTCTCCCC | 22937 |
rs200769720 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47473102 | AAAAAAAAAAAAACA[A/C/T]ACTGTGGAAGCAGGT | 22937 |
rs200779032 | in-del | -/TT | | | intron-variant | SCAP | GRCh38.p7 | 3:47445121 | AATGGGTATGCCACA[-/TT]TTGTTTGTCCATTCA | 22937 |
rs200779259 | in-del | -/A | | | intron-variant | SCAP | GRCh38.p7 | 3:47434837 | GCAAAACTCCATCTC[-/A]AAAAAAAAATGTATA | 22937 |
rs200867262 | snp | C/T | 0.00260996 | 0.0360301 | intron-variant | SCAP | GRCh38.p7 | 3:47418615 | CTACCCGTCCCCCTC[C/T]CCGCACTCTTTCCCA | 22937 |
rs200875447 | in-del | -/TGATC | | | intron-variant | SCAP | GRCh38.p7 | 3:47438431 | AGAAACGACTACAAG[-/TGATC]AGAATTCATTTAGGG | 22937 |
rs200883497 | in-del | -/CCG | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | PTPN23, SCAP | GRCh38.p7 | 3:47413807 | TTCAGTGCATTGGCC[-/CCG]CCCACACAGCACCCC | 22937 |
rs200905944 | snp | A/C | | | intron-variant | SCAP | GRCh38.p7 | 3:47473080 | AGCGAAACTCCATCT[A/C]AAAAAAAAAAAAAAA | 22937 |
rs200956092 | snp | C/G | 0.00299543 | 0.0385842 | intron-variant, upstream-variant-2KB | SCAP | GRCh38.p7 | 3:47425642 | GGCGTATCAGGGCGG[C/G]CCCTCCCCCAGCCCC | 22937 |
rs200960547 | snp | C/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47455643 | AAATCTCTGAAACTC[C/T]GAAAGACAGAAAAGA | 22937 |
rs200972311 | snp | C/T | 0.000555899 | 0.0166626 | missense | SCAP | GRCh38.p7 | 3:47420603 | AGGAAGTAGACAACA[C/T]GCAGCCTCTTGGGGA | 22937 |
rs201070946 | snp | A/C | | | intron-variant, upstream-variant-2KB | SCAP, LOC105377073 | GRCh38.p7 | 3:47474264 | AGCGAGACTCCATCT[A/C]AAAAAAAAAAAGAAA | 22937 |
rs201086219 | snp | C/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47460965 | AAGAGATGAGGCTCA[C/T]CTGGGCCCCTTTTCC | 22937 |
rs201148221 | snp | C/T | 0.000762903 | 0.0195159 | missense | SCAP | GRCh38.p7 | 3:47414586 | CCTGGTCAATGTACA[C/T]GGTCGTGATGGCCCC | 22937 |
rs201155936 | snp | A/C | | | missense | SCAP | GRCh38.p7 | 3:47420996 | GAAGGAAGAAGTCAG[A/C]CACCAGCCCCACGAC | 22937 |
rs201231966 | snp | G/T | 0.000116512 | 0.00763168 | missense | SCAP | GRCh38.p7 | 3:47414265 | CTGATGACACAGGAG[G/T]TGGTACAGGTAAGGG | 22937 |
rs201260839 | snp | A/G | 0.00398401 | 0.0444537 | intron-variant | SCAP | GRCh38.p7 | 3:47417104 | GGGACATCTGGGGCT[A/G]AGGCAGGCCACGCTC | 22937 |
rs201263232 | snp | C/T | 3.31268e-05 | 0.00406968 | synonymous-codon, intron-variant, upstream-variant-2KB | SCAP | GRCh38.p7 | 3:47426100 | CACGTGGACCAGGCT[C/T]TCCGCCCGAAGGCTG | 22937 |
rs201267449 | snp | C/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47455617 | AAAAAAAAAAAAAAA[C/T]AAACCAAAAGAAATC | 22937 |
rs201269608 | snp | C/G | 3.36457e-05 | 0.00410143 | intron-variant | SCAP | GRCh38.p7 | 3:47428494 | GATTCAGGGAGGCCA[C/G]GGTCCCTGAGAGGGG | 22937 |
rs201271939 | snp | C/T | 1.65343e-05 | 0.00287521 | utr-variant-5-prime, missense | SCAP | GRCh38.p7 | 3:47442971 | CGAGATATCTTCTCA[C/T]GCAGCCTTTCAGTCA | 22937 |
rs201451588 | snp | C/T | 1.74668e-05 | 0.00295518 | missense | SCAP | GRCh38.p7 | 3:47414981 | GCAGGGGAACTGCCC[C/T]GCCCTGGGGTCCCTG | 22937 |
rs201478816 | snp | C/T | 0.000378072 | 0.0137438 | synonymous-codon | SCAP | GRCh38.p7 | 3:47418447 | CTGCCCGTAGTTGCG[C/T]GGGCATAGCACGCGG | 22937 |
rs201484527 | snp | A/G | 0.000418379 | 0.0144573 | synonymous-codon | SCAP | GRCh38.p7 | 3:47417199 | CACCCCTTCAATGGC[A/G]TCCCACACCTACGAG | 22937 |
rs201494816 | snp | C/T | 6.63713e-05 | 0.00576032 | missense | SCAP | GRCh38.p7 | 3:47414042 | AGACACAGCCCTGGC[C/T]GCCAGTCACCAGCAG | 22937 |
rs201544029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47433125 | TTAAGTCAGCCCTGC[A/G]CCTGGCTGAGTTATA | 22937 |
rs201556579 | in-del | -/GGC | | | intron-variant | SCAP | GRCh38.p7 | 3:47451209 | AAAGCACACAAATTA[-/GGC]TAAGCACACAGCTCC | 22937 |
rs201558727 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | SCAP | GRCh38.p7 | 3:47440519 | AATTAAAAAAAAAAC[-/T]TTAAGATCACATGAC | 22937 |
rs201610129 | in-del | -/AAGAGA | | | intron-variant | SCAP | GRCh38.p7 | 3:47438427 | GAGAGAAACGACTAC[-/AAGAGA]AAGTGATCAGAATTC | 22937 |
rs201644938 | snp | A/C | | | intron-variant, upstream-variant-2KB | SCAP | GRCh38.p7 | 3:47425982 | AAGCCCTCAGCCTCC[A/C]TGCCATGAACCTACG | 22937 |
rs201655319 | snp | A/G | 0.000721858 | 0.0189844 | intron-variant, upstream-variant-2KB | SCAP | GRCh38.p7 | 3:47425630 | GAGGGCAGAGAGGGC[A/G]TATCAGGGCGGCCCC | 22937 |
rs201732400 | snp | C/T | 8.036e-05 | 0.00633826 | intron-variant | SCAP | GRCh38.p7 | 3:47415228 | CCCTTAGAGCCCCAG[C/T]CCTGGGGCTGAGCAT | 22937 |
rs201856241 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon | SCAP | GRCh38.p7 | 3:47414880 | CAGCAGCGGCTTTCA[A/G]GGCTGTGATGGGTTT | 22937 |
rs201870004 | in-del | -/A | | | intron-variant | SCAP | GRCh38.p7 | 3:47466129 | GAGTGAGACTGTCTT[-/A]AAAAACCAAAAAAAA | 22937 |
rs201879911 | snp | A/C/G/T | 0.00134363 | 0.0258909 | intron-variant | SCAP | GRCh38.p7 | 3:47423927 | CCAACTCTCCCACTG[A/C/G/T]GTTACCTTGGGCGAT | 22937 |
rs201890887 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47431009 | CAGAGGCAACCGTCT[C/G]AGCCTTTGTGAACTT | 22937 |
rs201900900 | snp | A/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47448728 | TCTGATTTTCTGTTC[A/T]TTTCAAGAGCATTCA | 22937 |
rs201938511 | snp | A/G | | | intron-variant | SCAP | GRCh38.p7 | 3:47432333 | AAAAAAAAAAAAAAA[A/G]AAAAGAAAAAGGAAA | 22937 |
rs201957604 | in-del | -/C | | | intron-variant, upstream-variant-2KB | SCAP, LOC105377073 | GRCh38.p7 | 3:47475169 | CTCACTGCCCCCCCC[-/C]TCCGCATTCCCATCT | 22937 |
rs201990086 | in-del | -/ATATATATAT | | | intron-variant | SCAP | GRCh38.p7 | 3:47455063 | ATACAAAAAAATTAC[-/ATATATATAT]ATATATATATATATA | 22937 |
rs201996918 | in-del | -/TAC | | | intron-variant | SCAP | GRCh38.p7 | 3:47450288 | AGGTGTGAGCCACTG[-/TAC]CTCCTGGCCCTAAGG | 22937 |
rs202026725 | snp | C/T | 0.000197658 | 0.00993931 | intron-variant, synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | SCAP | GRCh38.p7 | 3:47427481 | CTGCAGGGTTTTAGG[C/T]TCGTGCTGGTGGATG | 22937 |
rs202080098 | snp | C/T | 0.000216889 | 0.0104114 | missense | SCAP | GRCh38.p7 | 3:47420690 | CTCACAGCCAGCTGC[C/T]GCTCGTAGCGCGTTG | 22937 |
rs202089530 | in-del | -/T | 0.0150606 | 0.0854603 | intron-variant | SCAP | GRCh38.p7 | 3:47416553 | CCCCACTGTCACTGC[-/T]TTAAGGCCCTGGGAG | 22937 |
rs202138249 | snp | A/G | 0.000399281 | 0.0141238 | missense | SCAP | GRCh38.p7 | 3:47417135 | ACCTTTTGTCCAAGA[A/G]CACCAGAGCGGTAAT | 22937 |
rs202229681 | snp | A/G | 9.98868e-05 | 0.00706636 | intron-variant, utr-variant-5-prime | SCAP | GRCh38.p7 | 3:47434929 | AGCTGACCAACCTCA[A/G]TCTCACTGGCAGACC | 22937 |
rs207463139 | snp | C/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47438854 | AGGCTGTGGCTACAG[C/T]GTTTGCATAGTAATC | 22937 |
rs367551139 | snp | A/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47471618 | TCAGGTGATCCACCC[A/T]CCTCAGCCTCCCAAA | 22937 |
rs367563390 | snp | A/C | | | intron-variant | SCAP | GRCh38.p7 | 3:47457601 | TCAAGCGGACCAATG[A/C]TAAGGGCAGAAAATT | 22937 |
rs367570814 | snp | C/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47446531 | GTTGGGGTTTTTGTA[C/T]TTTTTTTCTTTTTGT | 22937 |
rs367786459 | snp | A/G | | | intron-variant | SCAP | GRCh38.p7 | 3:47416906 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC | 22937 |
rs367788810 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SCAP | GRCh38.p7 | 3:47447650 | CCAAAGACTGTGCCA[C/T]TGCACTCCAGCCTGG | 22937 |
rs367794799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47464309 | GCGTGAGCCACTGCA[C/T]CAGGCTTTTTTTATT | 22937 |
rs367896018 | snp | C/T | 1.75118e-05 | 0.00295898 | missense | SCAP | GRCh38.p7 | 3:47414985 | GGGAACTGCCCCGCC[C/T]TGGGGTCCCTGAGGA | 22937 |
rs367956537 | snp | A/G | 5.69893e-05 | 0.00533773 | intron-variant | SCAP | GRCh38.p7 | 3:47427675 | TCCCAGAGCTGCACA[A/G]GAGACAGGACAAGGC | 22937 |
rs367963303 | snp | C/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47463972 | ACACTGCTGGGACTA[C/T]AGGCATGAGCCACCA | 22937 |
rs367964689 | snp | A/G | | | intron-variant | SCAP | GRCh38.p7 | 3:47449663 | AAGATGGCTTCTGTT[A/G]GACCTCTTTCTGTGC | 22937 |
rs367966593 | snp | A/G | | | intron-variant | SCAP | GRCh38.p7 | 3:47430500 | CAGGAGGGAATGTGA[A/G]TTGCAAGGGATGCTG | 22937 |
rs367967894 | snp | C/T | 7.78468e-05 | 0.00623837 | missense | SCAP | GRCh38.p7 | 3:47417323 | AGCCGGCCGCTGCTC[C/T]GCCCCACCACGATGA | 22937 |
rs367980307 | snp | C/G | | | intron-variant | SCAP | GRCh38.p7 | 3:47431266 | GAACTCCCACAATCC[C/G]TACTTTACAGCACAA | 22937 |
rs368062445 | multinucleotide-polymorphism | GA/TT | | | upstream-variant-2KB, intron-variant, nc-transcript-variant | SCAP, LOC105377073 | GRCh38.p7 | 3:47476284 | ACTTGGGCAACGTAG[GA/TT]GACCTCCGTCTCCAC | 22937 |
rs368066222 | snp | C/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47461761 | AGTCTAGGCCGGGCA[C/T]GGTGGCTCACTCTTA | 22937 |
rs368067426 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47461537 | ACCAGATTTCAGAGC[C/T]AGGAGAGATGGGATC | 22937 |
rs368071859 | snp | C/T | 3.3605e-05 | 0.00409895 | missense | SCAP | GRCh38.p7 | 3:47417126 | GCCACGCTCACCTTT[C/T]GTCCAAGAACACCAG | 22937 |
rs368256276 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47429265 | TAGCACATTGGGCAG[C/T]GAGCCTCTTTTGCTC | 22937 |
rs368390058 | snp | C/T | 1.74668e-05 | 0.00295518 | intron-variant | SCAP | GRCh38.p7 | 3:47414798 | CGTGCCGGGCCACTC[C/T]AGCACCCAAGAGACA | 22937 |
rs368534243 | snp | A/C/T | 3.59266e-05 | 0.00423816 | intron-variant | SCAP | GRCh38.p7 | 3:47419294 | GTGAGTTGACACCAT[A/C/T]GAGTGAGGTGGCACC | 22937 |
rs368548171 | snp | C/T | 1.65332e-05 | 0.00287512 | synonymous-codon, intron-variant | SCAP | GRCh38.p7 | 3:47423955 | GATCCGCAGCTTCAC[C/T]TCCAGGTCTACCGGG | 22937 |
rs368573167 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAP | GRCh38.p7 | 3:47422113 | TGCACAGCCAGTCCC[C/T]AGCTCCTGCCATGCC | 22937 |
rs368604537 | snp | A/C | | | intron-variant | SCAP | GRCh38.p7 | 3:47472099 | GCACTCCAGCCTGGG[A/C]AACAGATTGAGTGAG | 22937 |
rs368631326 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SCAP, LOC105377073 | GRCh38.p7 | 3:47477981 | TTACCTATCCTGACA[C/T]CACTCTCTCCAGGTC | 22937 |
rs368653657 | snp | C/T | 1.66846e-05 | 0.00288826 | missense | SCAP | GRCh38.p7 | 3:47420699 | AGCTGCCGCTCGTAG[C/T]GCGTTGGCTGTCCCA | 22937 |
rs368667083 | snp | A/C | 0.00332511 | 0.0406387 | missense | SCAP | GRCh38.p7 | 3:47417407 | GCGAGGGAAGGGGAG[A/C]CTTTCTCGGGGGAGC | 22937 |
rs368681594 | snp | A/C/G | 4.9549e-05 | 0.00497719 | intron-variant | SCAP | GRCh38.p7 | 3:47420919 | GCAGGGCAGGGCTCA[A/C/G]CCCACTCCTACCTCC | 22937 |
rs368689544 | snp | C/T | 1.745e-05 | 0.00295376 | intron-variant | SCAP | GRCh38.p7 | 3:47415082 | GTGAACACCTGCCCA[C/T]CCCAGGCCCTCCGAC | 22937 |
rs368709955 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | SCAP | GRCh38.p7 | 3:47419299 | TTGACACCATCGAGT[A/G]AGGTGGCACCTGGCA | 22937 |
rs368756779 | snp | A/G | 0.00021268 | 0.0103099 | synonymous-codon | SCAP | GRCh38.p7 | 3:47418459 | GCGCGGGCATAGCAC[A/G]CGGTAGAGGCAGAGC | 22937 |
rs368775385 | snp | G/T | 1.70554e-05 | 0.00292017 | intron-variant | SCAP | GRCh38.p7 | 3:47422404 | GAGCACAGCAGTTGC[G/T]TCCATGCTCATCCAG | 22937 |
rs368841608 | snp | A/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47451826 | CAAAGCCCAAATGCC[A/T]CCCCCTAGCTCTCAG | 22937 |
rs368860161 | snp | A/G | | | upstream-variant-2KB, intron-variant | SCAP, LOC105377073 | GRCh38.p7 | 3:47478568 | ACCTCCCCCTCCCAG[A/G]TTCAAGTGATTCTCC | 22937 |
rs368862410 | snp | C/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47416052 | TGGTGACAGGAATGA[C/T]GGCAGCAGCCCACTG | 22937 |
rs368868479 | snp | A/G | 8.24396e-05 | 0.00641973 | intron-variant, missense, utr-variant-5-prime | SCAP | GRCh38.p7 | 3:47428535 | TCAGCACGTGGTTCC[A/G]GATCTCCTCCACCAG | 22937 |
rs368946042 | snp | A/G | 0.000181508 | 0.00952475 | missense | SCAP | GRCh38.p7 | 3:47419476 | GACCTCCACGCTCAG[A/G]TGACTCGCCTGGCGA | 22937 |
rs369030908 | snp | C/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47468168 | TATTGTGAATAGTGC[C/T]GTAATAAACATACGT | 22937 |
rs369092906 | in-del | -/ACATAC | | | intron-variant | SCAP | GRCh38.p7 | 3:47435466 | ACATATATAATATAA[-/ACATAC]ACACACACACACACA | 22937 |
rs369093642 | snp | A/G | 0.000165085 | 0.00908378 | missense | SCAP | GRCh38.p7 | 3:47417720 | GGTGTCTCAGGGGAG[A/G]GCTGTCCCCAGGCTC | 22937 |
rs369097240 | in-del | -/A | | | intron-variant | SCAP | GRCh38.p7 | 3:47462754 | GCGAAACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 22937 |
rs369100563 | snp | A/G | | | intron-variant | SCAP | GRCh38.p7 | 3:47457839 | ATGAACCCGGGAGGC[A/G]GAGCTTGCAGTGAGC | 22937 |
rs369138562 | snp | C/T | 0.0001331 | 0.00815674 | utr-variant-5-prime | SCAP | GRCh38.p7 | 3:47443023 | ACCTTGCTGCCATCC[C/T]GGAAAGTGACCATGG | 22937 |
rs369180354 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAP | GRCh38.p7 | 3:47433762 | AGTCCCAGGTACTCA[C/G]GAGGCTGAGGCAGGA | 22937 |
rs369219838 | snp | G/T | | | intron-variant | SCAP | GRCh38.p7 | 3:47451950 | CATTCCCATCTCAGG[G/T]GCCTGGCACATACTG | 22937 |
rs369222944 | snp | A/G | 0.000250815 | 0.0111957 | synonymous-codon | SCAP | GRCh38.p7 | 3:47418498 | CACCAAGACGATGCC[A/G]GTGGCCAGGCCCAGC | 22937 |
rs369235077 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, intron-variant, upstream-variant-2KB | SCAP | GRCh38.p7 | 3:47426010 | ACGCGTGGAGAAGTA[A/G]ATGTAGGCAAACAAG | 22937 |
rs369248739 | snp | A/G | | | intron-variant | SCAP | GRCh38.p7 | 3:47414784 | TCAGGCTCCCACCCC[A/G]TGCCGGGCCACTCCA | 22937 |
rs369326131 | snp | A/G | 6.67869e-05 | 0.00577832 | missense | SCAP | GRCh38.p7 | 3:47419364 | TAATAGCTGAAGAGC[A/G]TCGGCCAGTGGCGGA | 22937 |
rs369413571 | snp | A/G | | | intron-variant | SCAP | GRCh38.p7 | 3:47446595 | ATTGCTTGGTCATAA[A/G]GTAATTTTCCCCAAT | 22937 |
rs369499149 | snp | C/G/T | 0.000199112 | 0.00997611 | intron-variant | SCAP | GRCh38.p7 | 3:47414565 | ACCCCACCTGCAGGC[C/G/T]GCTTACCTGGTCAAT | 22937 |