SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs15139 | snp | G/T | 0 | 0 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105894119 | AAGGAAAAAGAAAAT[G/T]CAATTTCTTCATAAA | 8440 |
rs714068 | snp | C/T | 0.297382 | 0.245469 | intron-variant | NCK2 | GRCh38.p7 | 2:105791468 | GCACCCTCGCCCCGT[C/T]GCCGTGCTTACCGGC | 8440 |
rs714355 | snp | C/T | 0.370772 | 0.218893 | intron-variant | NCK2 | GRCh38.p7 | 2:105791252 | GAATGTTGATTCATC[C/T]AGAGAAACCTGAGGC | 8440 |
rs717730 | snp | A/G | 0.123452 | 0.215605 | intron-variant | NCK2 | GRCh38.p7 | 2:105750900 | ACGATCACAGAGATG[A/G]CAGGCTCAGAGGAGA | 8440 |
rs746436 | snp | C/G | 0.394372 | 0.233857 | intron-variant | NCK2 | GRCh38.p7 | 2:105789999 | GAGTCCAACACTAGC[C/G]TGTTCATGTATTGAG | 8440 |
rs746437 | snp | A/G | 0.419296 | 0.183954 | intron-variant | NCK2 | GRCh38.p7 | 2:105790216 | CCTAATGACATGCAC[A/G]CTATTTCTAACGGTT | 8440 |
rs768003 | snp | G/T | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105868384 | GGCAACTGTTCATAA[G/T]TTAAAGGCTGGGGTG | 8440 |
rs879900 | snp | C/T | 0.433527 | 0.169758 | intron-variant | NCK2 | GRCh38.p7 | 2:105877891 | GGGCAACTTCTTAAT[C/T]TGTGGAAATAAGGAA | 8440 |
rs905084 | snp | C/T | 0.491885 | 0.0631791 | intron-variant | NCK2 | GRCh38.p7 | 2:105768278 | GCCACCGGCCACACG[C/T]GGCCACTGAGCACTC | 8440 |
rs934305 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | NCK2 | GRCh38.p7 | 2:105845463 | gaggatgcagtgagt[A/G]aagatcagtcactgc | 8440 |
rs934306 | snp | G/T | 0.408359 | 0.193449 | intron-variant | NCK2 | GRCh38.p7 | 2:105843198 | TGAAACATAAATAAG[G/T]TATATATGAAACATA | 8440 |
rs934307 | snp | A/C | 0.26271 | 0.249677 | intron-variant | NCK2 | GRCh38.p7 | 2:105809340 | AATTGCTGTGTAAGC[A/C]CCTCAGTCTGTGGTA | 8440 |
rs997136 | snp | C/T | 0.499992 | 0.00199679 | intron-variant | NCK2 | GRCh38.p7 | 2:105749565 | TCCTTCTGCAGGCCA[C/T]ACATGAGGAACACCA | 8440 |
rs997522 | snp | A/G | 0.499933 | 0.00579035 | intron-variant | NCK2 | GRCh38.p7 | 2:105749775 | TGTCCCCACATCCTG[A/G]TTATGGGCCAGGGTT | 8440 |
rs1012028 | snp | C/G | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105760706 | ACCAGTTACAGCTGA[C/G]AACCCTATTGTGGAA | 8440 |
rs1052624 | snp | G/T | 0 | 0 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893800 | GAAAGACAGATGTTT[G/T]GGTAATTTACCCCAA | 8440 |
rs1076069 | snp | A/G | 0.25634 | 0.24992 | intron-variant | NCK2 | GRCh38.p7 | 2:105812545 | CTGAACGGGAGATCC[A/G]CTTGCAGGCCTCTGC | 8440 |
rs1114475 | snp | G/T | 0.489083 | 0.0730708 | intron-variant | NCK2 | GRCh38.p7 | 2:105759776 | TTTCTTAGACTCGCC[G/T]TGTTTTTAATGGCTT | 8440 |
rs1114882 | snp | A/G | 0.488424 | 0.0751925 | intron-variant | NCK2 | GRCh38.p7 | 2:105760112 | aggaagagggagttc[A/G]gctgtacctcctgta | 8440 |
rs1367404 | snp | G/T | 0.499816 | 0.0095829 | intron-variant | NCK2 | GRCh38.p7 | 2:105770408 | ATCTTTTGAGAGGTA[G/T]ATTTATGTGTCCTGA | 8440 |
rs1367405 | snp | A/G | 0.499809 | 0.00978247 | intron-variant | NCK2 | GRCh38.p7 | 2:105770684 | TATTGCCTAGGATAT[A/G]GATATCGATATTTAG | 8440 |
rs1367406 | snp | A/G | 0.0887219 | 0.191022 | intron-variant | NCK2 | GRCh38.p7 | 2:105803946 | ACTCACAAGGCACAT[A/G]GTATCCTCAGCTTTC | 8440 |
rs1465639 | snp | A/G | 0.433818 | 0.169443 | intron-variant | NCK2 | GRCh38.p7 | 2:105822725 | AATGGAATGTTATGT[A/G]TTCAGTTTCTATCTA | 8440 |
rs1465640 | snp | A/G | 0.425123 | 0.178415 | intron-variant | NCK2 | GRCh38.p7 | 2:105822647 | TCTTCAGCTTTCTAG[A/G]AAGCCACACTGCTAG | 8440 |
rs1465641 | snp | A/G | 0.433818 | 0.169443 | intron-variant | NCK2 | GRCh38.p7 | 2:105822480 | GGCGCTGTGGGAAGC[A/G]TCAGGGACCTTAGAG | 8440 |
rs1549768 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105819343 | TCTACCCCAATGACT[C/T]TTTTTTTTTTTTTTT | 8440 |
rs1549769 | snp | G/T | 0.256897 | 0.249905 | intron-variant | NCK2 | GRCh38.p7 | 2:105812862 | AGTTTGTTTTCAACG[G/T]TACTGCTTCTCTTAG | 8440 |
rs1549770 | snp | G/T | 0.402982 | 0.197728 | intron-variant | NCK2 | GRCh38.p7 | 2:105812811 | AAAAAAAAAAAGCCT[G/T]GTTGAATAGTGTCAC | 8440 |
rs1549771 | snp | A/G | 0.0865458 | 0.189163 | intron-variant | NCK2 | GRCh38.p7 | 2:105784039 | ATGGTGTTGAGGCCA[A/G]CCAGGTGCCACAGAA | 8440 |
rs1594403 | snp | C/G | 0.0785177 | 0.181917 | intron-variant | NCK2 | GRCh38.p7 | 2:105833928 | atgcaaattaaacaa[C/G]ttgctcttgaatgaa | 8440 |
rs1864555 | snp | C/T | 0.0883596 | 0.190715 | intron-variant | NCK2 | GRCh38.p7 | 2:105804449 | TTAGCTGTGTAAGCA[C/T]TTCCAAAGCCAAAAC | 8440 |
rs1897169 | snp | C/T | 0.499722 | 0.0117779 | | | GRCh38.p7 | 2:105781167 | ACACAAAGGCACCTC[C/T]AGGAAATGGGAAGCT | 8440 |
rs1986014 | snp | A/G | 0.338976 | 0.23363 | intron-variant | NCK2 | GRCh38.p7 | 2:105760506 | ACCTCCATCCTTGCC[A/G]TTCACACCTCTTCCC | 8440 |
rs1986015 | snp | A/G | 0.338523 | 0.233803 | intron-variant | NCK2 | GRCh38.p7 | 2:105760625 | CTTTGTATCAACCAA[A/G]GGTCTTTGCTTTCTG | 8440 |
rs2033008 | snp | A/T | 0.436834 | 0.166111 | intron-variant | NCK2 | GRCh38.p7 | 2:105886129 | GTGCCTGTAGGCATC[A/T]TTCCAGTTTCAAAGA | 8440 |
rs2047699 | snp | A/G | 0.420255 | 0.183066 | intron-variant | NCK2 | GRCh38.p7 | 2:105796620 | CAAATGCAAAAGGAA[A/G]AAAAGCACCATCTCC | 8440 |
rs2060036 | snp | C/T | 0.40086 | 0.199352 | intron-variant | NCK2 | GRCh38.p7 | 2:105819644 | TGTCTACGTGGCACC[C/T]GTGTGTTGGGAGCTC | 8440 |
rs2060037 | snp | C/G | 0.0607341 | 0.163335 | intron-variant | NCK2 | GRCh38.p7 | 2:105811848 | GGTCAATCGATGGGC[C/G]AAACCCCTATTAACT | 8440 |
rs2062657 | snp | C/T | 0.300673 | 0.244811 | intron-variant | NCK2 | GRCh38.p7 | 2:105777201 | TTCCTAAAGCAGCAG[C/T]GACGAGAGTAGAAGG | 8440 |
rs2082183 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | NCK2 | GRCh38.p7 | 2:105843864 | ggaagtctccaggaa[C/T]agcccacgcttaagg | 8440 |
rs2082184 | snp | A/G | 0.077417 | 0.180873 | intron-variant | NCK2 | GRCh38.p7 | 2:105840531 | gtcaacagtgtcaga[A/G]ctgaattaaattagc | 8440 |
rs2099211 | snp | A/G | 0.0807149 | 0.183963 | intron-variant | NCK2 | GRCh38.p7 | 2:105843673 | atattgctttttctt[A/G]aattgttccagcttt | 8440 |
rs2134082 | snp | C/G | 0.338976 | 0.23363 | intron-variant | NCK2 | GRCh38.p7 | 2:105760626 | CCAGAAAGCAAAGAC[C/G]CTTGGTTGATACAAA | 8440 |
rs2163349 | snp | C/T | 0.427727 | 0.175821 | intron-variant | NCK2 | GRCh38.p7 | 2:105841192 | AAAAGGTTACATGCC[C/T]GTGAGACTTTGGTTA | 8440 |
rs2163350 | snp | C/T | 0.238749 | 0.249747 | intron-variant | NCK2 | GRCh38.p7 | 2:105828825 | GGCCACTGGGTACAG[C/T]TGAAAAGATGAGTGA | 8440 |
rs2173883 | snp | C/G | 0.373397 | 0.217424 | intron-variant | NCK2 | GRCh38.p7 | 2:105760504 | GAAGAGGTGTGAACG[C/G]CAAGGATGGAGGTGA | 8440 |
rs2376977 | snp | A/G | 0.0905309 | 0.192535 | intron-variant | NCK2 | GRCh38.p7 | 2:105791634 | TTTCGAACTGACTCC[A/G]TAATAGATCTGATCA | 8440 |
rs2377338 | snp | A/G | 0.112631 | 0.208878 | intron-variant | NCK2 | GRCh38.p7 | 2:105834818 | tgggcctacaggtag[A/G]tgtgtgctaccatgt | 8440 |
rs2377339 | snp | A/G | 0.0685596 | 0.171987 | intron-variant | NCK2 | GRCh38.p7 | 2:105840835 | gaggctgaatcttgc[A/G]tcccccttttcctaa | 8440 |
rs2377340 | snp | A/G | 0.310632 | 0.242536 | intron-variant | NCK2 | GRCh38.p7 | 2:105844270 | gtagtgtgggatcct[A/G]ggtgggatcttggga | 8440 |
rs2553069 | snp | C/T | 0.0799831 | 0.183287 | | | GRCh38.p7 | 2:105873081 | CCCAGTTCCATGATC[C/T]TTGGCCAGCAGTCAG | 8440 |
rs2889526 | snp | A/T | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105755410 | ATTTGTTGCTTCTTA[A/T]CTTGATTGTGCCGAG | 8440 |
rs2889602 | snp | C/G | 0.397633 | 0.201754 | intron-variant | NCK2 | GRCh38.p7 | 2:105812620 | GCATTTGAGAGCTCT[C/G]AGGCCTATGCTAATC | 8440 |
rs2889603 | snp | A/G | 0.132751 | 0.2208 | intron-variant | NCK2 | GRCh38.p7 | 2:105831217 | tacctaaagtgatct[A/G]tacattcagtgcaat | 8440 |
rs2889604 | snp | C/T | 0.40263 | 0.198 | intron-variant | NCK2 | GRCh38.p7 | 2:105832076 | aatgtagacatcttt[C/T]actttcttggttaaa | 8440 |
rs3047649 | in-del | -/CCC | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105812789 | TCTGCTCATTACTGA[-/CCC]AGCCAGGTGACACTA | 8440 |
rs3047655 | in-del | -/AT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105844769 | TATATATATATATAT[-/AT]GTATGTATGTATATA | 8440 |
rs3047674 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105845398 | CATTTATATTTTGAA[-/T]TTTTTTTTTTTTTTT | 8440 |
rs3073520 | in-del | -/TGAA | 0.420344 | 0.182983 | intron-variant | NCK2 | GRCh38.p7 | 2:105757955 | CACAGCTGGGGTGAA[-/TGAA]GCACCTCTATTCTCT | 8440 |
rs3073523 | in-del | -/A/AA/AAA | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105779324 | AAAAAAAAAAAAAAA[-/A/AA/AAA]GAATCCGTCATAAAA | 8440 |
rs3073525 | in-del | -/CTTAGGC | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105786865 | ACCCTAGCCTTAGGC[-/CTTAGGC]TGACTCCCTTACCTC | 8440 |
rs3739131 | snp | C/G | 0.1652 | 0.235179 | intron-variant | NCK2 | GRCh38.p7 | 2:105882203 | TGTTTGCTACTCCGT[C/G]ATTTACTTGCATCTG | 8440 |
rs3754801 | snp | C/T | 0.303688 | 0.244167 | intron-variant | NCK2 | GRCh38.p7 | 2:105876735 | TCATTAAAGTAAAAC[C/T]ACCTACTGCTTCCAG | 8440 |
rs3754802 | snp | C/T | 0.335101 | 0.23507 | intron-variant | NCK2 | GRCh38.p7 | 2:105872939 | GACAGGCGCTGCTAA[C/T]GTCCACTTCCGGGAA | 8440 |
rs3754803 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105871340 | TGATCAGTAACCAGC[A/C]CTACAATAACGTGGC | 8440 |
rs3754804 | snp | A/G | 0.16618 | 0.23553 | intron-variant | NCK2 | GRCh38.p7 | 2:105871324 | CTACAATAACGTGGC[A/G]CAGCGCCTGACAGCA | 8440 |
rs3754805 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105871090 | TTCACACGCACTCAT[C/T]GACCCTCCAGGCCTG | 8440 |
rs3754806 | snp | C/T | 0.305685 | 0.24372 | intron-variant | NCK2 | GRCh38.p7 | 2:105870926 | ACCAAGATCCTACGA[C/T]GTGCTGGGCACTCAC | 8440 |
rs3754807 | snp | A/T | 0.304188 | 0.244057 | intron-variant | NCK2 | GRCh38.p7 | 2:105852877 | AGGATAAAGTTTACA[A/T]GAAGCTCCTATCAGA | 8440 |
rs3754808 | snp | C/T | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105852454 | ACTGCAAGCCAATTA[C/T]ATCAGTATCTTTATG | 8440 |
rs3769485 | snp | C/T | 0.420574 | 0.182769 | intron-variant | NCK2 | GRCh38.p7 | 2:105763648 | GGGTTGGGTTGTGCA[C/T]TGGGAACTTAGGGGT | 8440 |
rs3769486 | snp | C/G | 0.439918 | 0.162576 | intron-variant | NCK2 | GRCh38.p7 | 2:105763744 | CTTTCTGATTCTCAG[C/G]CGTGTTGTGGCAAAA | 8440 |
rs3769487 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | NCK2 | GRCh38.p7 | 2:105891172 | GGGAGTATGTGAGTA[C/T]TGAGAGTGTGTGAGA | 8440 |
rs3769488 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105891083 | AGCCCTCTGGACAAT[A/G]TGGAGCTGAGCATGT | 8440 |
rs3769489 | snp | C/T | 0.335788 | 0.23482 | intron-variant | NCK2 | GRCh38.p7 | 2:105890968 | CCCAGACCAGTTTTC[C/T]GCTTTTCTCAAAGCC | 8440 |
rs3769490 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | NCK2 | GRCh38.p7 | 2:105890729 | GAGAAGACTCAAATT[A/G]TGCAAGGCAGCTGGG | 8440 |
rs3769491 | snp | A/G | 0.335788 | 0.23482 | intron-variant | NCK2 | GRCh38.p7 | 2:105890197 | AGCAATAAAATTTTC[A/G]CAGCAGAAGAGGTAA | 8440 |
rs3769492 | snp | C/T | 0.336017 | 0.234736 | intron-variant | NCK2 | GRCh38.p7 | 2:105890171 | GGTAATTTTTAATTT[C/T]GTGGGCTCCTGAGCA | 8440 |
rs3769493 | snp | C/G | 0.230017 | 0.2492 | intron-variant | NCK2 | GRCh38.p7 | 2:105890151 | CCTTAACTTTTAAAG[C/G]TTTCTGCTCAGGAGC | 8440 |
rs3769494 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105888003 | TGGTGTTCAACAAAC[A/G]TGCAGACTTAAAAAT | 8440 |
rs3769495 | snp | C/G | 0.317933 | 0.240593 | intron-variant | NCK2 | GRCh38.p7 | 2:105887720 | TGTTTTCTCATAGAA[C/G]GAAAAAAATGAATGC | 8440 |
rs3769496 | snp | C/T | 0.165853 | 0.235413 | intron-variant | NCK2 | GRCh38.p7 | 2:105879420 | GCAGGATGGTTCAAC[C/T]ACACAATGAAAGCAC | 8440 |
rs3769497 | snp | G/T | 0.0995161 | 0.199636 | intron-variant | NCK2 | GRCh38.p7 | 2:105873565 | AAACGTGGTAAATAT[G/T]GGTGAGCTGAAAAGA | 8440 |
rs3769498 | snp | C/T | 0.304438 | 0.244001 | intron-variant | NCK2 | GRCh38.p7 | 2:105871955 | CACCAATTTCCCTTG[C/T]ACGAAATCTCAGCCC | 8440 |
rs3769499 | snp | C/T | 0.0850919 | 0.187897 | intron-variant | NCK2 | GRCh38.p7 | 2:105864989 | GAGGGCTCTGGTGAC[C/T]GCTTTTTAGTTGAAG | 8440 |
rs3769500 | snp | C/T | 0.303688 | 0.244167 | intron-variant | NCK2 | GRCh38.p7 | 2:105864968 | TTAGTTGAAGGTACT[C/T]GTGTTATTTGGATGG | 8440 |
rs3769501 | snp | C/G | 0.108402 | 0.206034 | intron-variant | NCK2 | GRCh38.p7 | 2:105863350 | GACAACTGAAGCTTA[C/G]ACTCGGCTTCCACGA | 8440 |
rs3769502 | snp | C/T | 0.470521 | 0.117772 | intron-variant | NCK2 | GRCh38.p7 | 2:105862295 | CTAACCTGGGTCTTT[C/T]GATCTAAGTAAAATC | 8440 |
rs3769503 | snp | A/G | 0.0788843 | 0.182262 | intron-variant | NCK2 | GRCh38.p7 | 2:105860829 | GGAATGGTTAATCCA[A/G]GCATGAGAGGCAATC | 8440 |
rs3769504 | snp | C/T | 0.478603 | 0.101197 | intron-variant | NCK2 | GRCh38.p7 | 2:105860636 | ATGCCCCTGCTCAAA[C/T]CTTCAACTGTTTGTG | 8440 |
rs3820890 | snp | C/T | 0.429987 | 0.173507 | intron-variant | NCK2 | GRCh38.p7 | 2:105879837 | CTTTCTCCTTTTCTT[C/T]CTTAAACTAGAGTAA | 8440 |
rs3832068 | in-del | -/T/TT/TTT | 0.561358 | 0.185895 | intron-variant | NCK2 | GRCh38.p7 | 2:105855369 | ACTTTTAAAACAGAC[-/T/TT/TTT]TTTTTTTTTTTTGAA | 8440 |
rs3834120 | in-del | -/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105884241 | GCAGTGGATGGTGGG[-/G]AAAAAAACAAGCAAA | 8440 |
rs3835868 | in-del | -/TG | 0.439918 | 0.162576 | intron-variant | NCK2 | GRCh38.p7 | 2:105763601 | TTGTGTTCTGGGATC[-/TG]TGATTATTTACTGTT | 8440 |
rs3835869 | in-del | -/T | 0.0898077 | 0.191933 | intron-variant | NCK2 | GRCh38.p7 | 2:105888309 | GACCACTTCTTCCTG[-/T]TATGTCCTTCTATGA | 8440 |
rs3835871 | in-del | -/AAT | 0.0792508 | 0.182605 | intron-variant | NCK2 | GRCh38.p7 | 2:105856332 | TAAGAAGGTAACAAC[-/AAT]GTTTTAAATGTCAGC | 8440 |
rs3929435 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105761542 | actgtcccag[A/C/T] | 8440 |
rs3954042 | snp | C/T | 0.112983 | 0.209108 | intron-variant | NCK2 | GRCh38.p7 | 2:105836891 | gctacccagcatgaa[C/T]ggtctttctagagta | 8440 |
rs4012805 | in-del | -/AC/ACAA/ACAC/ACACACTA/ACACTA | | | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105894020 | CACACACACACACAC[-/AC/ACAA/ACAC/ACACACTA/ACACTA]TATATATATATATAT | 8440 |
rs4316956 | snp | C/G | 0.417196 | 0.185864 | intron-variant | NCK2 | GRCh38.p7 | 2:105789768 | GCTTTTTCTGACACA[C/G]ACTGCTGCCCCACAC | 8440 |
rs4330124 | snp | G/T | 0.140242 | 0.224618 | intron-variant | NCK2 | GRCh38.p7 | 2:105791461 | AGGGAGTGCACCCTC[G/T]CCCCGTTGCCGTGCT | 8440 |
rs4429493 | snp | C/G | 0.0785177 | 0.181917 | intron-variant | NCK2 | GRCh38.p7 | 2:105834908 | gtcttgaactcctgg[C/G]ctcaagcaatcctcc | 8440 |
rs4438502 | snp | A/C | 0.310632 | 0.242536 | intron-variant | NCK2 | GRCh38.p7 | 2:105844468 | GTGGCTCACGCCTGT[A/C]ATCTCAGCACTTTGG | 8440 |
rs4438503 | snp | A/C | 0.376394 | 0.215696 | intron-variant | NCK2 | GRCh38.p7 | 2:105844578 | GTAGAAAAAAACAAA[A/C]AAAAAAAAAAACAGC | 8440 |
rs4438504 | snp | A/C | 0.424968 | 0.178567 | intron-variant | NCK2 | GRCh38.p7 | 2:105844579 | tagaaaaaaacaaaa[A/C]aaaaaaaaaacagct | 8440 |
rs4627591 | snp | G/T | 0.337614 | 0.234145 | intron-variant | NCK2 | GRCh38.p7 | 2:105844358 | taatgtatgggtagt[G/T]gttcattaattgtaa | 8440 |
rs4851090 | snp | C/T | 0.286825 | 0.247273 | intron-variant | NCK2 | GRCh38.p7 | 2:105794929 | ACTACTCTCTCTATC[C/T]TCTTTTTTCCCTACT | 8440 |
rs4851091 | snp | C/T | 0.417359 | 0.185718 | intron-variant | NCK2 | GRCh38.p7 | 2:105802660 | ACCCACTCATCACCA[C/T]GAGGAAGGCACCATG | 8440 |
rs4851092 | snp | A/G | 0.267908 | 0.249358 | intron-variant | NCK2 | GRCh38.p7 | 2:105808655 | CACCCAGCGTCTTCA[A/G]TGCATTGTCATTAAA | 8440 |
rs4851094 | snp | C/T | 0.402277 | 0.198272 | intron-variant | NCK2 | GRCh38.p7 | 2:105838591 | AGACCCCTTATTATG[C/T]AGAATAACAATGAAT | 8440 |
rs4851095 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | NCK2 | GRCh38.p7 | 2:105839093 | gaggggacatttgaa[C/T]ggcggcttgaacaaa | 8440 |
rs4851838 | snp | A/C | 0.156319 | 0.231784 | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105746264 | GCCTAAAATATCGCA[A/C]GGGCCAGCTCCGTCC | 8440 |
rs4851840 | snp | C/G | 0.391769 | 0.205917 | intron-variant | NCK2 | GRCh38.p7 | 2:105752796 | TTTTATGGCTGAATA[C/G]TCTATTTTCTTTATC | 8440 |
rs4851841 | snp | A/G | 0.439363 | 0.163222 | intron-variant | NCK2 | GRCh38.p7 | 2:105757057 | TGATCTGCCTGCCTC[A/G]GCCTCCCAGAGTGCT | 8440 |
rs4851842 | snp | C/T | 0.287346 | 0.247195 | intron-variant | NCK2 | GRCh38.p7 | 2:105758643 | TTGAACTCCTGACCT[C/T]GTGATCCACCCGCCT | 8440 |
rs4851843 | snp | C/T | 0.43221 | 0.171171 | intron-variant | NCK2 | GRCh38.p7 | 2:105761884 | CCAAAAAAGACTGAA[C/T]ACAGACATGTGCGCT | 8440 |
rs4851844 | snp | A/C | 0.449979 | 0.150028 | intron-variant | NCK2 | GRCh38.p7 | 2:105762031 | TTTTTGCGTTGACTA[A/C]AGTTGCAAGTGTGGG | 8440 |
rs4851845 | snp | A/C | 0.43221 | 0.171171 | intron-variant | NCK2 | GRCh38.p7 | 2:105762156 | TCTTGGGTTTTCCTT[A/C]GAAGAAGCTTGTGAG | 8440 |
rs4851846 | snp | C/G | 0.440057 | 0.162414 | intron-variant | NCK2 | GRCh38.p7 | 2:105765146 | TGCCAGTTTTCAGTA[C/G]TGTGGAAGTATCAAT | 8440 |
rs4851847 | snp | C/T | 0.439918 | 0.162576 | intron-variant | NCK2 | GRCh38.p7 | 2:105766824 | TCCAAACTATTTCCA[C/T]CTGTAGTGAGTAGTG | 8440 |
rs4851848 | snp | A/G | 0.439918 | 0.162576 | intron-variant | NCK2 | GRCh38.p7 | 2:105766834 | TTCCATCTGTAGTGA[A/G]TAGTGTTAGTTTGAC | 8440 |
rs4851849 | snp | A/G | 0.43978 | 0.162738 | intron-variant | NCK2 | GRCh38.p7 | 2:105766854 | GTTAGTTTGACTTAC[A/G]AATTAATATTTAAGC | 8440 |
rs4851850 | snp | A/G | 0.43978 | 0.162738 | intron-variant | NCK2 | GRCh38.p7 | 2:105766911 | GAGGCTTCTGGCTCC[A/G]TCTTCCTGCTGCCTG | 8440 |
rs4851851 | snp | G/T | 0.440057 | 0.162414 | intron-variant | NCK2 | GRCh38.p7 | 2:105767032 | GTGTCACACCTACTC[G/T]TATGGTCAGCTACTC | 8440 |
rs4851852 | snp | A/G | 0.440195 | 0.162252 | intron-variant | NCK2 | GRCh38.p7 | 2:105767084 | CCCACACACACCAGT[A/G]CTGGGTTCCTGGTGC | 8440 |
rs4851853 | snp | C/T | 0.440195 | 0.162252 | intron-variant | NCK2 | GRCh38.p7 | 2:105767253 | TGAACCAAATGCAAT[C/T]TGCTGTTAATGTAAT | 8440 |
rs4851854 | snp | G/T | 0.440195 | 0.162252 | intron-variant | NCK2 | GRCh38.p7 | 2:105767281 | AATACTGCTCGTGAC[G/T]TGGCCTACTTGGATG | 8440 |
rs4851855 | snp | A/C | 0.440195 | 0.162252 | intron-variant | NCK2 | GRCh38.p7 | 2:105768016 | AAATGAAGACATCTC[A/C]AGCAGCACTGTCCAG | 8440 |
rs4851856 | snp | A/T | 0.439918 | 0.162576 | intron-variant | NCK2 | GRCh38.p7 | 2:105768041 | GTCCAGCAGAAATAG[A/T]ACATAAGCTGCCAGT | 8440 |
rs4851857 | snp | C/T | 0.440195 | 0.162252 | intron-variant | NCK2 | GRCh38.p7 | 2:105768060 | TAAGCTGCCAGTGTG[C/T]GCTAGATGTGTAACT | 8440 |
rs4851858 | snp | A/T | 0.440195 | 0.162252 | intron-variant | NCK2 | GRCh38.p7 | 2:105768296 | TGTGGCCGGTGGCTG[A/T]GTTATCAAACAGGTC | 8440 |
rs4851859 | snp | A/G | 0.440333 | 0.16209 | intron-variant | NCK2 | GRCh38.p7 | 2:105768423 | AAGTCCCACAAGACC[A/G]TCCCCATTTCCGTCA | 8440 |
rs4851860 | snp | C/T | 0.440333 | 0.16209 | intron-variant | NCK2 | GRCh38.p7 | 2:105768448 | ccgtcaccagttgca[C/T]gtcctaagccacctg | 8440 |
rs4851861 | snp | C/T | 0.420892 | 0.182472 | intron-variant | NCK2 | GRCh38.p7 | 2:105768478 | gtacttctgatcaac[C/T]ggctgtaaattgggg | 8440 |
rs4851862 | snp | C/T | 0.301681 | 0.2446 | intron-variant | NCK2 | GRCh38.p7 | 2:105773926 | CAAGACAAAACCCTC[C/T]GTTTATAAGAAAGAT | 8440 |
rs4851863 | snp | A/G | 0.421684 | 0.181726 | intron-variant | NCK2 | GRCh38.p7 | 2:105774715 | TGGGGCCTGGATGAC[A/G]AAATCTGTGTTCCAC | 8440 |
rs4851864 | snp | A/G | 0.301429 | 0.244653 | intron-variant | NCK2 | GRCh38.p7 | 2:105774881 | CCGTGTAGATGTACA[A/G]CTGAAAAAACGCTTT | 8440 |
rs4851865 | snp | C/T | 0.444444 | 0.157135 | intron-variant | NCK2 | GRCh38.p7 | 2:105780327 | GGAGAGAGATATATA[C/T]ACACACACACACACA | 8440 |
rs4851866 | snp | A/G | 0.496905 | 0.0392151 | intron-variant | NCK2 | GRCh38.p7 | 2:105780599 | AAACATCAGTCACCA[A/G]TCAGAGCCCCTGGTC | 8440 |
rs4851867 | snp | C/T | 0.429388 | 0.174127 | intron-variant | NCK2 | GRCh38.p7 | 2:105781775 | CGCCTCTCCGCAGTA[C/T]GAAAATTTGTAGACA | 8440 |
rs4851870 | snp | C/T | 0.32768 | 0.237625 | intron-variant | NCK2 | GRCh38.p7 | 2:105820800 | TTTTGGAGGCTTTTT[C/T]ATGACAGACATGTCC | 8440 |
rs4851871 | snp | A/G | 0.327914 | 0.237549 | intron-variant | NCK2 | GRCh38.p7 | 2:105822762 | TCAGTGATTCTCTGA[A/G]TTGTACCTTAGAATT | 8440 |
rs4851872 | snp | A/G | 0.412082 | 0.190341 | intron-variant | NCK2 | GRCh38.p7 | 2:105830832 | ttattggccatttgt[A/G]tatcttcttttgaga | 8440 |
rs4851875 | snp | A/G | 0.404209 | 0.196773 | intron-variant | NCK2 | GRCh38.p7 | 2:105833991 | ttttagttttattct[A/G]ttgtgttctgagata | 8440 |
rs4851876 | snp | A/T | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105835423 | tgtatatatatatat[A/T]ttttttttttggtca | 8440 |
rs4851877 | snp | A/C | 0.107341 | 0.205301 | intron-variant | NCK2 | GRCh38.p7 | 2:105838931 | AATGTGTGTGAAGTA[A/C]TGGTAAGGGCCATGG | 8440 |
rs4851878 | snp | A/G | 0.331411 | 0.236373 | intron-variant | NCK2 | GRCh38.p7 | 2:105845749 | AAGTACCTTACAGCT[A/G]TGAAAAAAAAATAGG | 8440 |
rs5833150 | in-del | -/T | 0.29432 | 0.24604 | intron-variant | NCK2 | GRCh38.p7 | 2:105765022 | TCTTCAGTGGAACCA[-/T]TTTTTTTTTTTTAGT | 8440 |
rs5833151 | in-del | -/GCCTTAG/GCCTTAGGCCTTAG | 0.560338 | 0.194299 | intron-variant | NCK2 | GRCh38.p7 | 2:105786856 | CCTGCTCCCACCCTA[-/GCCTTAG/GCCTTAGGCCTTAG]GCCTTAGGCTGACTC | 8440 |
rs5833152 | in-del | -/T/TT | 0.482159 | 0.0927485 | intron-variant | NCK2 | GRCh38.p7 | 2:105812815 | CTATTCAACAAGGCT[-/T/TT]TTTTTTTTTTTTTCC | 8440 |
rs5833159 | in-del | -/ACACTA | | | cds-indel | NCK2 | GRCh38.p7 | 2:105894017 | CACACACACACACAC[-/ACACTA]TATATATATATATTA | 8440 |
rs6543336 | snp | A/C | 0.293807 | 0.246132 | intron-variant | NCK2 | GRCh38.p7 | 2:105785518 | TACAAAATCTAATGC[A/C]GCCTGCCCAGTCCTC | 8440 |
rs6543337 | snp | C/G | 0.25912 | 0.249834 | intron-variant | NCK2 | GRCh38.p7 | 2:105786203 | AAACAATCCCAGCAC[C/G]AGGGATGAAAAAATT | 8440 |
rs6543338 | snp | C/G | 0.499087 | 0.0213463 | intron-variant | NCK2 | GRCh38.p7 | 2:105787454 | AGACAGCAGAGAGCT[C/G]TCTCTGCCACCTGAG | 8440 |
rs6543340 | snp | C/T | 0.254944 | 0.249951 | intron-variant | NCK2 | GRCh38.p7 | 2:105814844 | GACAGCCCAAACAAC[C/T]GCATAAAACAATTCC | 8440 |
rs6543341 | snp | C/G | 0.254385 | 0.249962 | intron-variant | NCK2 | GRCh38.p7 | 2:105815436 | ATTAATAGATCTTCT[C/G]TGAGTGAACTGTCAA | 8440 |
rs6543342 | snp | C/T | 0.404559 | 0.196498 | intron-variant | NCK2 | GRCh38.p7 | 2:105845800 | AAATGGTGACTGTTA[C/T]CCGTCTACTTTGGGA | 8440 |
rs6543343 | snp | C/T | 0.089084 | 0.191327 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105850971 | TCCAAGGGATGCAAC[C/T]TCAACTCTCGGCCAA | 8440 |
rs6543344 | snp | C/G | 0.164546 | 0.234942 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105851050 | CAAAGAGAGAAAAGA[C/G]CGAAGCCTGTGAGGA | 8440 |
rs6543345 | snp | C/T | 0.0894459 | 0.191631 | intron-variant | NCK2 | GRCh38.p7 | 2:105854937 | GACCCAGGAGAAAAC[C/T]GGTTGCAGAGTTGTA | 8440 |
rs6543346 | snp | A/G | 0.0883596 | 0.190715 | intron-variant | NCK2 | GRCh38.p7 | 2:105857452 | TCTTCCTTAAATAGA[A/G]TCAGATTTTTACATT | 8440 |
rs6543347 | snp | G/T | 0.0883596 | 0.190715 | intron-variant | NCK2 | GRCh38.p7 | 2:105857660 | ATGTTCTGAACCCCT[G/T]TATTGAGTATAGCAG | 8440 |
rs6543348 | snp | C/T | 0.316485 | 0.240998 | intron-variant | NCK2 | GRCh38.p7 | 2:105889676 | GTTGCCTTGACCTCC[C/T]GGGCTCAAGTGATCC | 8440 |
rs6704555 | snp | A/G | 0.0941369 | 0.195465 | intron-variant | NCK2 | GRCh38.p7 | 2:105861325 | CGATCTTTAAAGACA[A/G]TGTATACAGACGTCA | 8440 |
rs6706946 | snp | G/T | 0.392325 | 0.205532 | intron-variant | NCK2 | GRCh38.p7 | 2:105793592 | cagtatccaccaaag[G/T]gagcaatgaatttgt | 8440 |
rs6707820 | snp | C/T | 0.406814 | 0.194704 | intron-variant | NCK2 | GRCh38.p7 | 2:105809256 | TTCAAGTTCCTGTTG[C/T]GTGTGTCATATGTCG | 8440 |
rs6711659 | snp | A/T | 0.420733 | 0.18262 | intron-variant | NCK2 | GRCh38.p7 | 2:105794964 | TCCATCACCATTTTT[A/T]AAAGATGTTTTTTTC | 8440 |
rs6712210 | snp | A/G | 0.455383 | 0.142541 | intron-variant | NCK2 | GRCh38.p7 | 2:105832795 | ccttgtctgtttcag[A/G]tgtcaggataatact | 8440 |
rs6713106 | snp | C/T | 0.255224 | 0.249945 | intron-variant | NCK2 | GRCh38.p7 | 2:105805179 | TCCTAGAAGAGAGCA[C/T]GTTTGAGTTCCTTCC | 8440 |
rs6717125 | snp | A/G | 0.448195 | 0.152377 | intron-variant | NCK2 | GRCh38.p7 | 2:105817622 | aagtgggcaaaggat[A/G]tgaacagacactgct | 8440 |
rs6719259 | snp | C/T | 0.089084 | 0.191327 | intron-variant | NCK2 | GRCh38.p7 | 2:105852268 | GGCAGGTGCGCATCA[C/T]TGCTCAACATTTACT | 8440 |
rs6719896 | snp | C/G | 0.403158 | 0.197592 | intron-variant | NCK2 | GRCh38.p7 | 2:105811947 | CTAGAACTGACAGAC[C/G]TTAAACTCTAATCAG | 8440 |
rs6723057 | snp | C/T | 0.188 | 0.24219 | intron-variant | NCK2 | GRCh38.p7 | 2:105823025 | TAAATAAACAGGCCA[C/T]ACAGAGCTTGAAATG | 8440 |
rs6723369 | snp | A/G | 0.297382 | 0.245469 | intron-variant | NCK2 | GRCh38.p7 | 2:105773711 | AACAACTATTTGAGC[A/G]CCTACTCTGAGCCAG | 8440 |
rs6725519 | snp | C/T | 0.418974 | 0.184249 | intron-variant | NCK2 | GRCh38.p7 | 2:105828753 | GAGTGAAATAGGATG[C/T]TGCTGTGTTGACCTC | 8440 |
rs6726298 | snp | C/G | 0.0788843 | 0.182262 | intron-variant | NCK2 | GRCh38.p7 | 2:105859479 | CACACCTAGGCCTAG[C/G]GTGGTTAGAAACTTG | 8440 |
rs6726571 | snp | C/T | 0.499994 | 0.00179711 | intron-variant | NCK2 | GRCh38.p7 | 2:105773794 | TTGCTCCCCTGAGCT[C/T]GTGTCTGGCAGGCTG | 8440 |
rs6730190 | snp | A/G | 0.448066 | 0.152544 | intron-variant | NCK2 | GRCh38.p7 | 2:105817666 | ttatgcagccaaaag[A/G]cacatgaaaaaatgc | 8440 |
rs6730514 | snp | A/C | 0.303938 | 0.244112 | intron-variant | NCK2 | GRCh38.p7 | 2:105854524 | attgttattattatt[A/C]ttagactttattttg | 8440 |
rs6732664 | snp | C/T | 0.367091 | 0.220884 | intron-variant | NCK2 | GRCh38.p7 | 2:105785352 | AGAGGACGGTTCCCC[C/T]GTCCTGGCCAAGGAG | 8440 |
rs6732799 | snp | C/T | 0.367091 | 0.220884 | intron-variant | NCK2 | GRCh38.p7 | 2:105785497 | ACACGACCAAAAGAC[C/T]GCCAATACAAAATCT | 8440 |
rs6736701 | snp | G/T | 0.499995 | 0.00159744 | intron-variant | NCK2 | GRCh38.p7 | 2:105773983 | ATCTGGAAGTCCTCA[G/T]GTGGAAGATGTGGAT | 8440 |
rs6736932 | snp | A/G | 0.424348 | 0.179172 | intron-variant | NCK2 | GRCh38.p7 | 2:105828398 | ATTTGCCTGTAATTA[A/G]TGTTGGTCAAATTTA | 8440 |
rs6737260 | snp | A/T | 0.435694 | 0.167385 | intron-variant | NCK2 | GRCh38.p7 | 2:105822672 | TGAAGAAACAAAAAC[A/T]AAAAAGCCAATTCTG | 8440 |
rs6739170 | snp | C/G | 0.0887219 | 0.191022 | intron-variant | NCK2 | GRCh38.p7 | 2:105857185 | TCAGTTTTCTAGAAG[C/G]AGAAAAGACAAAGCC | 8440 |
rs6740208 | snp | A/T | 0.0883596 | 0.190715 | intron-variant | NCK2 | GRCh38.p7 | 2:105858840 | TAATTTAAAATTGAT[A/T]AAAGCAACCTGAGCT | 8440 |
rs6740343 | snp | A/G | 0.463451 | 0.130149 | intron-variant | NCK2 | GRCh38.p7 | 2:105889022 | GGTCCTTTTTCATCC[A/G]ATTTCTTGAAATCTG | 8440 |
rs6741172 | snp | A/G | 0.445592 | 0.155704 | intron-variant | NCK2 | GRCh38.p7 | 2:105823603 | GGAATGAATTCTGGG[A/G]CCATGTTAACAAAGA | 8440 |
rs6741223 | snp | C/T | 0.256619 | 0.249912 | intron-variant | NCK2 | GRCh38.p7 | 2:105812619 | GGCATTTGAGAGCTC[C/T]GAGGCCTATGCTAAT | 8440 |
rs6745887 | snp | A/G | 0.436265 | 0.166749 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105851583 | TTCTAAGGGTCTTGG[A/G]AAGTGTGGCTTCCAG | 8440 |
rs6747023 | snp | A/G | 0.412917 | 0.189626 | intron-variant | NCK2 | GRCh38.p7 | 2:105815399 | TATTTAACATTTTGG[A/G]TCATAATCATGCTAG | 8440 |
rs6749913 | snp | A/G | 0.238749 | 0.249747 | intron-variant | NCK2 | GRCh38.p7 | 2:105828387 | AATTCACAATAATTT[A/G]CCTGTAATTAATGTT | 8440 |
rs6752445 | snp | G/T | 0.0887219 | 0.191022 | intron-variant | NCK2 | GRCh38.p7 | 2:105855789 | TCAGAGGCCGCTCCA[G/T]GGTGGGGGCCTAGTT | 8440 |
rs6752686 | snp | C/T | 0.0883596 | 0.190715 | intron-variant | NCK2 | GRCh38.p7 | 2:105855927 | GCAAGCTCCACCTCC[C/T]GGGTTCACACCATTC | 8440 |
rs6753494 | snp | A/G | 0.33303 | 0.235809 | intron-variant | NCK2 | GRCh38.p7 | 2:105889149 | GAGTTGTTTTGGGTC[A/G]GGAGTAACTCCATCT | 8440 |
rs6753511 | snp | A/G | 0.332337 | 0.236052 | intron-variant | NCK2 | GRCh38.p7 | 2:105889179 | TCCATCAGATGCAGG[A/G]ACTGGTGGCTCACTT | 8440 |
rs6754967 | snp | C/G | 0.0221141 | 0.102801 | intron-variant | NCK2 | GRCh38.p7 | 2:105884339 | CCACTAGGCCACCAA[C/G]AGCCCTTAGGTTCAT | 8440 |
rs6760834 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | NCK2 | GRCh38.p7 | 2:105834057 | ttcgtttatgaccaa[A/G]catactgtaaatcct | 8440 |
rs6761169 | snp | G/T | 0.0919752 | 0.193722 | intron-variant | NCK2 | GRCh38.p7 | 2:105793241 | gaatgggtggagaac[G/T]tctggaaaccagagt | 8440 |
rs7423628 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105777355 | agggtagcttTCAGG[C/T]ACAGAGGAGGGCTGG | 8440 |
rs7423816 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105868505 | ATAGTTGTTGATTGT[C/G]TGATTTGTGAAATTT | 8440 |
rs7557976 | snp | A/C | 0.401392 | 0.198948 | intron-variant | NCK2 | GRCh38.p7 | 2:105818604 | TAATCAAAGCATAAC[A/C]TAAATTAGTTTTGGT | 8440 |
rs7559524 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105835367 | cttggctggttttat[A/G]tatatatacatatat | 8440 |
rs7562054 | snp | C/G | 0.4021 | 0.198407 | intron-variant | NCK2 | GRCh38.p7 | 2:105817056 | TGGCGTGCACATGTA[C/G]TCTCAGCTATTCGGG | 8440 |
rs7562892 | snp | C/T | 0.499809 | 0.00978247 | intron-variant | NCK2 | GRCh38.p7 | 2:105779755 | GACCATGATTTAAAA[C/T]GCACACTCACATACA | 8440 |
rs7563690 | snp | C/T | 0.499891 | 0.00738737 | intron-variant | NCK2 | GRCh38.p7 | 2:105780478 | GCTTCTCGCTCATGT[C/T]CTGTGTCACATCCAT | 8440 |
rs7564056 | snp | C/T | 0.226484 | 0.248892 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105744738 | GCGCCCCAGGTGGGT[C/T]TCGGGTccccgcccc | 8440 |
rs7565757 | snp | A/T | 0.455383 | 0.142541 | intron-variant | NCK2 | GRCh38.p7 | 2:105835952 | tttaattcatttaat[A/T]attcagttccaagac | 8440 |
rs7566776 | snp | C/T | 0.396546 | 0.202545 | intron-variant | NCK2 | GRCh38.p7 | 2:105811002 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 8440 |
rs7571132 | snp | C/T | 0.499587 | 0.0143711 | intron-variant | NCK2 | GRCh38.p7 | 2:105782456 | AGTCTATATAATGAA[C/T]GCTCTTTTCTTAAGT | 8440 |
rs7573751 | snp | A/G | 0.427879 | 0.175668 | intron-variant | NCK2 | GRCh38.p7 | 2:105840893 | cagccaggtccccac[A/G]gaaaggtaaaaggcc | 8440 |
rs7574253 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | NCK2 | GRCh38.p7 | 2:105782867 | ACTTACTGTCCCCAA[C/T]GCTCCCAACTGGAGA | 8440 |
rs7574880 | snp | G/T | 0.0267878 | 0.112589 | intron-variant | NCK2 | GRCh38.p7 | 2:105835902 | ttctttcttctgctt[G/T]atctagtctcttttt | 8440 |
rs7580718 | snp | A/C | 0.403158 | 0.197592 | intron-variant | NCK2 | GRCh38.p7 | 2:105854871 | TTGCTGTTTCTAAAC[A/C]AAATACTAAAGCTTG | 8440 |
rs7581087 | snp | C/T | 0.0456336 | 0.143994 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105745150 | CGAGGTAAGCGCGGC[C/T]AGGCGGGCGTGGGGC | 8440 |
rs7582886 | snp | C/G | 0.200801 | 0.245111 | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105743241 | GGGCCACTGGATTTA[C/G]ATAGAGAATGACATC | 8440 |
rs7585909 | snp | A/G | 0.214843 | 0.247516 | intron-variant | NCK2 | GRCh38.p7 | 2:105827890 | atagtcttgattggc[A/G]tggtggttataggag | 8440 |
rs7588033 | snp | C/T | 0.390277 | 0.206936 | intron-variant | NCK2 | GRCh38.p7 | 2:105791776 | TCCATGTAAAAATGA[C/T]GCAGCTGCTCGTGGT | 8440 |
rs7589272 | snp | G/T | 0.387263 | 0.208947 | intron-variant | NCK2 | GRCh38.p7 | 2:105780319 | ATAATATGGGAGAGA[G/T]ATATATACACACACA | 8440 |
rs7589342 | snp | C/T | 0.4021 | 0.198407 | intron-variant | NCK2 | GRCh38.p7 | 2:105817021 | AAGATAAATCTGTGT[C/T]AAAGGATAGCTGGGC | 8440 |
rs7589561 | snp | C/T | 0.112631 | 0.208878 | intron-variant | NCK2 | GRCh38.p7 | 2:105837629 | taagtagaagtggag[C/T]tgctgCCTTGTACgt | 8440 |
rs7589589 | snp | C/G | 0.499598 | 0.0141716 | intron-variant | NCK2 | GRCh38.p7 | 2:105774697 | AGGAGGTGTCAAGTT[C/G]TCTGGGGCCTGGATG | 8440 |
rs7589790 | snp | C/G | 0.412249 | 0.190198 | intron-variant | NCK2 | GRCh38.p7 | 2:105817452 | TTAATCCGGTGTTCT[C/G]TTTCTGGCTGGGCAG | 8440 |
rs7589902 | snp | C/G | 0.301681 | 0.2446 | intron-variant | NCK2 | GRCh38.p7 | 2:105837963 | CTTATATATTCAACA[C/G]CAGTCCTGTACGATT | 8440 |
rs7590652 | snp | A/G | 0.425432 | 0.178112 | intron-variant | NCK2 | GRCh38.p7 | 2:105823850 | CTGCAAGCAGTAAGG[A/G]TGATCCTAATTATGA | 8440 |
rs7595024 | snp | A/G | 0.255224 | 0.249945 | intron-variant | NCK2 | GRCh38.p7 | 2:105814709 | AAAACCTTTAGTGTC[A/G]CTGAGAAAGTGAACT | 8440 |
rs7595703 | snp | A/G | 0.498871 | 0.0237351 | intron-variant | NCK2 | GRCh38.p7 | 2:105785169 | ATTTTTAGTAGAGAC[A/G]GGATTTCACTGTGTT | 8440 |
rs7595710 | snp | A/G | 0.363985 | 0.222503 | intron-variant | NCK2 | GRCh38.p7 | 2:105785192 | ACTGTGTTAGCCAGG[A/G]TGGTCTCCATCTCCT | 8440 |
rs7598962 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105835376 | ttttatatatatata[C/T]atatatatacacata | 8440 |
rs7598964 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105835386 | atatacatatatata[C/T]acatatatatatata | 8440 |
rs7598966 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105835388 | atacatatatataca[C/T]atatatatatatata | 8440 |
rs7598970 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105835406 | atatatatatatata[C/T]gtgtatatatatata | 8440 |
rs7599123 | snp | A/G | 0.249886 | 0.25 | intron-variant | NCK2 | GRCh38.p7 | 2:105815924 | GAGGAAGTCTGGAAG[A/G]GACTGGGAGCTCAGG | 8440 |
rs7601328 | snp | A/C | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105862465 | ACAGCAGTCACAGGT[A/C]CGAGACCCAGAGGGG | 8440 |
rs7601645 | snp | A/G | 0.431325 | 0.172108 | intron-variant | NCK2 | GRCh38.p7 | 2:105889131 | TGGCTCCCTCTGGAG[A/G]CAGAGTTGTTTTGGG | 8440 |
rs7602442 | snp | C/T | 0.499137 | 0.0207489 | intron-variant | NCK2 | GRCh38.p7 | 2:105786338 | ACGGACTTGTTCCAT[C/T]AGCCCTGGGAACGGC | 8440 |
rs7602971 | snp | A/G | 0.459801 | 0.135955 | intron-variant | NCK2 | GRCh38.p7 | 2:105824219 | ATAGCAGAATGCCCC[A/G]TCCGTAAATGTCACG | 8440 |
rs7604409 | snp | C/G | 0.223522 | 0.248594 | intron-variant | NCK2 | GRCh38.p7 | 2:105754451 | TATCTTAAGAATTTT[C/G]GTTGCGTGTTTAAGG | 8440 |
rs7605092 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | NCK2 | GRCh38.p7 | 2:105798515 | TTAGAGAGAAGAAAT[A/G]AGGGTTAAAATTGTT | 8440 |
rs9646946 | snp | A/G | 0.0883596 | 0.190715 | intron-variant | NCK2 | GRCh38.p7 | 2:105861490 | AAAGTGATAGTGGCT[A/G]TTGGTGCCGTTGAGG | 8440 |
rs9646959 | snp | A/G | 0.349452 | 0.229367 | intron-variant | NCK2 | GRCh38.p7 | 2:105795734 | CGACAAAGAATTACC[A/G]AAACGTCTGTATGCC | 8440 |
rs9646960 | snp | C/T | 0.0799831 | 0.183287 | intron-variant | NCK2 | GRCh38.p7 | 2:105861583 | GCAGTGGCACAATCT[C/T]GGCTCACTGCAACCT | 8440 |
rs9653481 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105889588 | ttttttttttttttt[A/T]ttttaattattttga | 8440 |
rs9973371 | snp | A/G | 0.029116 | 0.117091 | intron-variant | NCK2 | GRCh38.p7 | 2:105762411 | TTTGAAAGGGGTTCA[A/G]TCTGTCTCTTCTGTA | 8440 |
rs10167046 | snp | A/G | 0.499809 | 0.00978247 | intron-variant | NCK2 | GRCh38.p7 | 2:105770307 | ATTGAAATTTCTGTT[A/G]CAGTGTGACTCCAGT | 8440 |
rs10168919 | snp | A/G | 0.209388 | 0.246679 | intron-variant | NCK2 | GRCh38.p7 | 2:105792445 | tcctgtaaatattac[A/G]gaatTTCaataacaa | 8440 |
rs10168944 | snp | C/T | 0.499809 | 0.00978247 | intron-variant | NCK2 | GRCh38.p7 | 2:105769610 | GACGTGTGGGTGACC[C/T]ACTGCACTGCCCACT | 8440 |
rs10169688 | snp | G/T | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105835291 | tccaatttttgcttg[G/T]ctgggaaagactttt | 8440 |
rs10169998 | snp | A/G | 0.421684 | 0.181726 | intron-variant | NCK2 | GRCh38.p7 | 2:105835797 | aggatcccacatgtc[A/G]ggtaggctttcttca | 8440 |
rs10173137 | snp | A/C | 0.499809 | 0.00978247 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771592 | GACCTAATTTAGACA[A/C]ATATTTCAAGAAGTT | 8440 |
rs10177819 | snp | A/G | 0.499859 | 0.0083854 | intron-variant | NCK2 | GRCh38.p7 | 2:105770183 | AAGGATGGTGCTGTG[A/G]ACATGGGGTGTGGTT | 8440 |
rs10177914 | snp | G/T | 0.499816 | 0.0095829 | intron-variant | NCK2 | GRCh38.p7 | 2:105770236 | AGACTTCAAAAAAAT[G/T]TTAATATTCTGGACA | 8440 |
rs10178047 | snp | A/G | 0.498794 | 0.0245311 | intron-variant | NCK2 | GRCh38.p7 | 2:105835409 | tatatatatatacgt[A/G]tatatatatatatat | 8440 |
rs10178272 | snp | A/C | 0.0509478 | 0.151255 | intron-variant | NCK2 | GRCh38.p7 | 2:105777195 | CTGGAACCTTCTACT[A/C]TCGTCACTGCTGCTT | 8440 |
rs10180659 | snp | C/T | 0.398894 | 0.200825 | intron-variant | NCK2 | GRCh38.p7 | 2:105848917 | ACAGTATTTTTCATA[C/T]AGACTCAATTTTTTT | 8440 |
rs10185551 | snp | A/C | 0.443866 | 0.157848 | intron-variant | NCK2 | GRCh38.p7 | 2:105875745 | CTCCAGAATGGTGAG[A/C]AATAAATGTCTGTAA | 8440 |
rs10192144 | snp | A/G | 0.433963 | 0.169285 | intron-variant | NCK2 | GRCh38.p7 | 2:105823398 | CCATTCCCGTGCTGC[A/G]GGTGCCTCACTGGAC | 8440 |
rs10196773 | snp | A/G | 0.171704 | 0.237423 | intron-variant | NCK2 | GRCh38.p7 | 2:105781039 | GTCTCTCACCTGGTC[A/G]TGGTCTTCCTGTCTT | 8440 |
rs10198057 | snp | G/T | 0.499793 | 0.0101816 | intron-variant | NCK2 | GRCh38.p7 | 2:105776342 | ATTTCAACATCTTCT[G/T]GAAGCAGCCAAAGCA | 8440 |
rs10200841 | snp | C/T | 0.440609 | 0.161766 | intron-variant | NCK2 | GRCh38.p7 | 2:105839931 | CGCGCAGCTGGTGGA[C/T]GGTGTGTTTCCCAGA | 8440 |
rs10201738 | snp | C/T | 0.499809 | 0.00978247 | intron-variant | NCK2 | GRCh38.p7 | 2:105769837 | CTCAGATTTTAATCC[C/T]TCGGAGTAATCTTTG | 8440 |
rs10203262 | snp | C/T | 0.163236 | 0.234461 | intron-variant | NCK2 | GRCh38.p7 | 2:105765394 | TGCCAGTAGTGCTCA[C/T]GGATTTAGCATTCCA | 8440 |
rs10469861 | snp | A/G | 0.0535932 | 0.154675 | intron-variant | NCK2 | GRCh38.p7 | 2:105795580 | TTACATGTATGCTCC[A/G]Tcagtggttctcagc | 8440 |
rs10469862 | snp | C/T | 0.424814 | 0.178718 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893451 | CTCGTGCATTCAACT[C/T]GTTCCCGCTCATGGA | 8440 |
rs10490695 | snp | G/T | 0.348354 | 0.22984 | intron-variant | NCK2 | GRCh38.p7 | 2:105888539 | CAATCATAGAAAATT[G/T]TAATGAGTGTCCTGT | 8440 |
rs10496402 | snp | A/G | 0.136847 | 0.222927 | intron-variant | NCK2 | GRCh38.p7 | 2:105754856 | AGTGAATTTTCATCA[A/G]ACGATTAAAAAAAAG | 8440 |
rs10496403 | snp | G/T | 0.350982 | 0.228698 | intron-variant | NCK2 | GRCh38.p7 | 2:105803165 | GTATCACAAATTAGT[G/T]TTTATCTAAGATAGT | 8440 |
rs10524426 | in-del | -/ACACACACACACACACACAC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105864829 | CTCACATGTGCATGT[-/ACACACACACACACACACAC]ACACACACACACACA | 8440 |
rs10610689 | in-del | -/TGTGTGTGTG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105823133 | AAAGTCCTCTCATGC[-/TGTGTGTGTG]TGTGTGTGTGTGTGT | 8440 |
rs10622924 | in-del | -/AAAG | 0.0785177 | 0.181917 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893735 | GGCTGTGCTTGCAAT[-/AAAG]AAAGAATTTCCTGGA | 8440 |
rs10639030 | in-del | -/AA | | | intron-variant | NCK2 | GRCh38.p7 | 2:105817189 | AAAAAAAAAAAAAAA[-/AA]CCTACATCAAATGAG | 8440 |
rs10645562 | in-del | -/AGAA | 0 | 0 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893741 | GCTTGCAATAAAGAA[-/AGAA]TTTCCTGGAAAGGCA | 8440 |
rs10666166 | in-del | -/AGAG | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105891573 | TTTTTTTTTTGAGAT[-/AGAG]TTTTCGCTCTTGTTG | 8440 |
rs10865069 | snp | C/T | 0.300673 | 0.244811 | intron-variant | NCK2 | GRCh38.p7 | 2:105775456 | TAACTTCAGATTGAT[C/T]TTGTTTGAACTTAAT | 8440 |
rs10865070 | snp | A/G | 0.0599851 | 0.162463 | intron-variant | NCK2 | GRCh38.p7 | 2:105830396 | GTTGCCATGAGTGAC[A/G]AGTGACAGAATTTTA | 8440 |
rs11124057 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | NCK2 | GRCh38.p7 | 2:105783461 | ACAGCTCGATGCAGC[A/G]TTGCCTGTCTGAGCC | 8440 |
rs11124058 | snp | A/G | 0.495521 | 0.0471118 | intron-variant | NCK2 | GRCh38.p7 | 2:105784292 | TAATAGGAAGTTGCC[A/G]TCCCTTTTCTCACCC | 8440 |
rs11124059 | snp | C/G | 0.389715 | 0.207315 | intron-variant | NCK2 | GRCh38.p7 | 2:105797484 | GCAGGCTGCCAGGCT[C/G]TGCGGGCTAGCAGAA | 8440 |
rs11124060 | snp | A/G | 0.45866 | 0.137698 | intron-variant | NCK2 | GRCh38.p7 | 2:105827161 | cctaccaccacgccc[A/G]gctaatttttggtat | 8440 |
rs11124061 | snp | A/G | 0.458545 | 0.137872 | intron-variant | NCK2 | GRCh38.p7 | 2:105827221 | agccaggatggtctc[A/G]atctcctgacctcgt | 8440 |
rs11124062 | snp | A/G | 0.432797 | 0.170544 | intron-variant | NCK2 | GRCh38.p7 | 2:105839511 | cagattgggggctgg[A/G]tcagcccacttaatg | 8440 |
rs11124063 | snp | C/T | 0.405776 | 0.195535 | intron-variant | NCK2 | GRCh38.p7 | 2:105842350 | CTCAGCCTCTCAAAG[C/T]GTTGGGATTACAGGC | 8440 |
rs11124064 | snp | C/T | 0.391397 | 0.206172 | intron-variant | NCK2 | GRCh38.p7 | 2:105842435 | ACACTGAGGAAAGTT[C/T]GTAACATTTTTTCCT | 8440 |
rs11124065 | snp | C/T | 0.089084 | 0.191327 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105850578 | TGTAGCCCTTCTCTC[C/T]TTGGGCTAGACCTGA | 8440 |
rs11358569 | in-del | -/A | 0.459801 | 0.135955 | intron-variant | NCK2 | GRCh38.p7 | 2:105811178 | CTGGTGACAGAGTGC[-/A]AAAAAAAAAAAAAAA | 8440 |
rs11385276 | in-del | -/C | 0.0618563 | 0.164627 | intron-variant | NCK2 | GRCh38.p7 | 2:105822179 | TGCAGTTTGGAGAGT[-/C]TCTTTGGAAACGTAA | 8440 |
rs11406827 | in-del | -/A | | | intron-variant | NCK2 | GRCh38.p7 | 2:105811178 | AAAAAAAAAAAAAAA[-/A]TGCATTATGGCTTTC | 8440 |
rs11434432 | in-del | -/T/TT | 0.625 | 0.125 | intron-variant | NCK2 | GRCh38.p7 | 2:105812829 | CTTTTTTTTTTTTTT[-/T/TT]CCCTCCTGTGCTAAC | 8440 |
rs11553852 | snp | C/T | 0 | 0 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881627 | GAGGCGGCTGCGGAG[C/T]CCCCAAGCTTCCTGA | 8440 |
rs11553853 | snp | G/T | | | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105894180 | CAATCGTAGGAATGT[G/T]CCATCTCAAGACGTT | 8440 |
rs11553854 | snp | A/G | 0 | 0 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881509 | CCTGGTGAAGGGGTC[A/G]CGCGTCACCGTCATG | 8440 |
rs11676842 | snp | A/G | 0.440057 | 0.162414 | intron-variant | NCK2 | GRCh38.p7 | 2:105766073 | CCTGACATTGCTACC[A/G]TGGATAGTAGAAATC | 8440 |
rs11676893 | snp | A/G | 0.440057 | 0.162414 | intron-variant | NCK2 | GRCh38.p7 | 2:105766175 | GGGGAAGTGGGGCCT[A/G]GGAAGCACATTCTGG | 8440 |
rs11677728 | snp | C/T | 0.305186 | 0.243833 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105851286 | TTTTTTTTTCTGAGA[C/T]GGAGTCTCGCTCTGT | 8440 |
rs11680781 | snp | G/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105773100 | gacaggccctcactg[G/T]gttatccaggctggt | 8440 |
rs11681797 | snp | A/G | 0.440057 | 0.162414 | intron-variant | NCK2 | GRCh38.p7 | 2:105765853 | TGTGGAGGTATGTGT[A/G]TTAGCTGTCTTTCAT | 8440 |
rs11681892 | snp | G/T | 0.440057 | 0.162414 | intron-variant | NCK2 | GRCh38.p7 | 2:105766025 | AGTTCCTGGTACTCT[G/T]GCCCAGACTTTGCTT | 8440 |
rs11683641 | snp | A/G | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105767451 | ACAGTAATTGATTTA[A/G]GAATATCTGTTACTC | 8440 |
rs11683858 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105824931 | ATCAGGAGCCCATCT[C/G]CCACCTGAGTCTCAA | 8440 |
rs11687998 | snp | C/T | 0.282105 | 0.24793 | intron-variant | NCK2 | GRCh38.p7 | 2:105767676 | TTCCAGAAGAAGAAC[C/T]GCAGCCCCTAGTGTG | 8440 |
rs11688046 | snp | A/C | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105884123 | TCTCCTGACAGCAGA[A/C]CCATGCCAGGTTTGC | 8440 |
rs11688108 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105884249 | TTTTTCCCACCATCC[A/G]CTGCCTCCCCCCGTC | 8440 |
rs11690510 | snp | C/T | 0.419456 | 0.183806 | intron-variant | NCK2 | GRCh38.p7 | 2:105830218 | ccaaccttttcctat[C/T]cctccctctccccac | 8440 |
rs11691815 | snp | C/T | 0.440057 | 0.162414 | intron-variant | NCK2 | GRCh38.p7 | 2:105764986 | CAAGGTGCCTGTGTA[C/T]GTCTCTGGGTATATT | 8440 |
rs11692954 | snp | A/T | 0.287085 | 0.247234 | intron-variant | NCK2 | GRCh38.p7 | 2:105756085 | TTGCTGTCTGAATGT[A/T]CTTTTTTTCTTTAAA | 8440 |
rs11693509 | snp | A/C | 0.440195 | 0.162252 | intron-variant | NCK2 | GRCh38.p7 | 2:105766063 | AGCAGGACTCCCTGA[A/C]ATTGCTACCATGGAT | 8440 |
rs11694185 | snp | A/G | 0.440195 | 0.162252 | intron-variant | NCK2 | GRCh38.p7 | 2:105768253 | GACATAGCTGGACTC[A/G]CCACCCCTTGAGTGC | 8440 |
rs11694417 | snp | A/T | 0.429087 | 0.174436 | intron-variant | NCK2 | GRCh38.p7 | 2:105762808 | TTTGGTGTGTTAATA[A/T]GGAAATACGTAGATT | 8440 |
rs11883807 | snp | C/T | 0.0659589 | 0.169201 | intron-variant | NCK2 | GRCh38.p7 | 2:105869272 | TCCTGCATGTGTCCC[C/T]AGCCATAACAGCGAA | 8440 |
rs11885225 | snp | C/T | 0.436692 | 0.166271 | intron-variant | NCK2 | GRCh38.p7 | 2:105870092 | AGAGCTGGTTCCTGG[C/T]GTGCCCACCCACTGG | 8440 |
rs11885238 | snp | G/T | 0.238749 | 0.249747 | intron-variant | NCK2 | GRCh38.p7 | 2:105826866 | GGATGGAAAAAGATA[G/T]ACCATGCAAATACTA | 8440 |
rs11886675 | snp | G/T | 0.349233 | 0.229462 | intron-variant | NCK2 | GRCh38.p7 | 2:105792661 | aaaacccggtctttt[G/T]tcatttgggcttccc | 8440 |
rs11887355 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NCK2 | GRCh38.p7 | 2:105842320 | tgaactcctgacctc[A/G]ggtgatctacctgcc | 8440 |
rs11889330 | snp | A/G | 0.330016 | 0.236849 | intron-variant | NCK2 | GRCh38.p7 | 2:105769594 | GTTTTCTAAGAAATG[A/G]GACGTGTGGGTGACC | 8440 |
rs11890447 | snp | C/T | 0.499631 | 0.0135733 | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105773234 | AGTGAGTGCCAAGGA[C/T]ATTTTTCTTTAAGAA | 8440 |
rs11893695 | snp | C/G | 0.363985 | 0.222503 | intron-variant | NCK2 | GRCh38.p7 | 2:105784843 | GTGTGTCCTCAGATA[C/G]TGACAGAATAGGATA | 8440 |
rs11894170 | snp | A/T | 0.331411 | 0.236373 | intron-variant | NCK2 | GRCh38.p7 | 2:105780589 | AATTATGCTGAAACA[A/T]CAGTCACCAGTCAGA | 8440 |
rs11895235 | snp | C/G | 0.412917 | 0.189626 | intron-variant | NCK2 | GRCh38.p7 | 2:105815898 | CTTTTAAAGGTGGGG[C/G]TCATTGGGAGGAGGA | 8440 |
rs11895542 | snp | A/G | 0.499631 | 0.0135733 | intron-variant | NCK2 | GRCh38.p7 | 2:105773972 | ATGAAGTGTGCATCT[A/G]GAAGTCCTCAGGTGG | 8440 |
rs11896455 | snp | A/G | 0.207559 | 0.246371 | intron-variant | NCK2 | GRCh38.p7 | 2:105820416 | ACACTCAAGGTTTGC[A/G]TGCCTGGGGCTGGGC | 8440 |
rs11900659 | snp | G/T | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105822894 | GCCTAGTACGGCCCA[G/T]CGTTGGATGGTGACC | 8440 |
rs11901644 | snp | G/T | 0.402982 | 0.197728 | intron-variant | NCK2 | GRCh38.p7 | 2:105815656 | CTCATCTTAACTTCC[G/T]TCTAGTTTTGGAGTG | 8440 |
rs11904001 | snp | A/G | 0.361474 | 0.223771 | intron-variant | NCK2 | GRCh38.p7 | 2:105785018 | GAGTCTCGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 8440 |
rs12052296 | snp | A/G | 0.440057 | 0.162414 | intron-variant | NCK2 | GRCh38.p7 | 2:105764522 | TGAGCAGGAGGCAGA[A/G]TGATACTGGTCACTT | 8440 |
rs12052297 | snp | A/G | 0.440057 | 0.162414 | intron-variant | NCK2 | GRCh38.p7 | 2:105764603 | CAAAGTGCAAACCAA[A/G]CACACAGCTGCTTTA | 8440 |
rs12053259 | snp | A/G | 0.402982 | 0.197728 | intron-variant | NCK2 | GRCh38.p7 | 2:105812263 | GATTAAGAGACAGCT[A/G]AGGTCATCTCCTTGG | 8440 |
rs12464067 | snp | A/G | 0.418491 | 0.184691 | intron-variant | NCK2 | GRCh38.p7 | 2:105799655 | GAATACCACTATATG[A/G]AAGCCTATAAAAAGC | 8440 |
rs12465089 | snp | C/T | 0.419616 | 0.183658 | intron-variant | NCK2 | GRCh38.p7 | 2:105770173 | CAACAAGAAAAAGGA[C/T]GGTGCTGTGGACATG | 8440 |
rs12468535 | snp | A/C | 0.430136 | 0.173352 | intron-variant | NCK2 | GRCh38.p7 | 2:105773571 | TCCTTCCCCTTCCCC[A/C]GTCCTCTGTCAGCAC | 8440 |
rs12469477 | snp | A/C | 0.298398 | 0.245271 | intron-variant | NCK2 | GRCh38.p7 | 2:105779920 | CGCCTTCACCCTCTC[A/C]TTCAGGATAGCGTGT | 8440 |
rs12470376 | snp | C/T | 0.298398 | 0.245271 | intron-variant | NCK2 | GRCh38.p7 | 2:105779921 | GCCTTCACCCTCTCA[C/T]TCAGGATAGCGTGTA | 8440 |
rs12475901 | snp | A/G | 0.229136 | 0.249128 | intron-variant | NCK2 | GRCh38.p7 | 2:105777237 | TGTCCCCATAGCCAC[A/G]AGCCGGGGTGTTGCG | 8440 |
rs12476157 | snp | C/T | 0.417683 | 0.185425 | intron-variant | NCK2 | GRCh38.p7 | 2:105800155 | GTAGCCTGGCTGCAC[C/T]GTATAGTCTGGCTCT | 8440 |
rs12478567 | snp | A/C | 0.440057 | 0.162414 | intron-variant | NCK2 | GRCh38.p7 | 2:105766564 | CTGGCCTTAAGGGAT[A/C]CTCCCACCTCAGCCT | 8440 |
rs12479197 | snp | A/T | 0.429087 | 0.174436 | intron-variant | NCK2 | GRCh38.p7 | 2:105763102 | ACTCAGGAGGCTGAG[A/T]CAGGAGAATTGCTTG | 8440 |
rs12479428 | snp | C/T | 0.421368 | 0.182025 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105772722 | ACTAGAGTTTTTCCC[C/T]GAAACTCTTCTTTCT | 8440 |
rs12613162 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105780329 | AGAGAGATATATaca[C/T]acacacacacacaca | 8440 |
rs12616493 | snp | C/T | 0.475525 | 0.107882 | intron-variant | NCK2 | GRCh38.p7 | 2:105759283 | CAAGTACACATAGTA[C/T]GTTCTCTGGGGAAAG | 8440 |
rs12622245 | snp | C/T | 0.238749 | 0.249747 | intron-variant | NCK2 | GRCh38.p7 | 2:105826008 | ATTGCTAGGATGGTC[C/T]ACATCCCTTAGAAGG | 8440 |
rs12623430 | snp | C/T | 0.112631 | 0.208878 | intron-variant | NCK2 | GRCh38.p7 | 2:105836751 | ctctttgggtggata[C/T]ggtgagatgttgaca | 8440 |
rs12712216 | snp | A/G | 0.15698 | 0.23205 | intron-variant | NCK2 | GRCh38.p7 | 2:105756214 | ATTTCCTGTTCCATT[A/G]TTCTTCCTTTTGACT | 8440 |
rs12712217 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | NCK2 | GRCh38.p7 | 2:105768833 | AAAGGAAGTGACACA[C/T]GGGACGAGGGGTGGG | 8440 |
rs12712218 | snp | G/T | 0.455502 | 0.142369 | intron-variant | NCK2 | GRCh38.p7 | 2:105835295 | atttttgcttgtctg[G/T]gaaagacttttattt | 8440 |
rs12712219 | snp | A/G | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105835389 | tacatatatatacac[A/G]tatatatatatatat | 8440 |
rs12712222 | snp | C/T | 0.482757 | 0.0912364 | intron-variant | NCK2 | GRCh38.p7 | 2:105859951 | GTTGGTATTATACTT[C/T]CGTTTTTAAGAAATT | 8440 |
rs12712223 | snp | C/G | 0.078151 | 0.181571 | intron-variant | NCK2 | GRCh38.p7 | 2:105892733 | TTCCTGTAATCCCAG[C/G]TACTCGGGAGGCCGA | 8440 |
rs12986783 | snp | A/G | 0.341909 | 0.232492 | intron-variant | NCK2 | GRCh38.p7 | 2:105764173 | TTGCACGCCTGTGCA[A/G]TGATCCTTGGTGTGG | 8440 |
rs12987484 | snp | C/T | 0.341235 | 0.232758 | intron-variant | NCK2 | GRCh38.p7 | 2:105751104 | CATTGATGCTTTGTT[C/T]GCTCATTCATTCACA | 8440 |
rs12989056 | snp | A/C | 0.324382 | 0.238678 | intron-variant | NCK2 | GRCh38.p7 | 2:105818519 | AAGAAATATATATTT[A/C]CAACATGGTATATTT | 8440 |
rs12989634 | snp | C/T | 0.43978 | 0.162738 | intron-variant | NCK2 | GRCh38.p7 | 2:105769013 | GCAGAAAGTTCCCAC[C/T]CTCTAATCACACGTT | 8440 |
rs12992852 | snp | A/G | 0.362941 | 0.223034 | intron-variant | NCK2 | GRCh38.p7 | 2:105892180 | CAAAAGCAAAACTGC[A/G]TCTCAAAAAAAAAAA | 8440 |
rs12992944 | snp | G/T | 0.35445 | 0.227135 | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105744218 | GCCTGGGAGGCAACA[G/T]AGGTCGAGTTTCTTC | 8440 |
rs12994173 | snp | C/G | 0.311123 | 0.242413 | intron-variant | NCK2 | GRCh38.p7 | 2:105861949 | TCCTGCCCGCTCCCC[C/G]CTTCCCTTTCTTCCA | 8440 |
rs12995333 | snp | G/T | 0.410905 | 0.191336 | intron-variant | NCK2 | GRCh38.p7 | 2:105819909 | CTTGCAGTGACTGTT[G/T]TAGCAGTTAAAAAAA | 8440 |
rs12995660 | snp | A/G | 0.327211 | 0.237778 | intron-variant | NCK2 | GRCh38.p7 | 2:105827289 | caggcgtgagccacc[A/G]cgcctggctgacata | 8440 |
rs12995849 | snp | C/T | 0.45866 | 0.137698 | intron-variant | NCK2 | GRCh38.p7 | 2:105826655 | ATTTGGGTTCTAGGC[C/T]CCCTGGATTTGGGTC | 8440 |
rs12996286 | snp | A/G | 0.318415 | 0.240457 | intron-variant | NCK2 | GRCh38.p7 | 2:105783210 | ATTTTCTTTAAGATG[A/G]TATGTAATCTTTTGA | 8440 |
rs12997003 | snp | C/T | 0.410905 | 0.191336 | intron-variant | NCK2 | GRCh38.p7 | 2:105819956 | GTCCCAGCCACCTTT[C/T]CCCATGCCCTTTCAG | 8440 |
rs12997041 | snp | C/T | 0.327445 | 0.237702 | intron-variant | NCK2 | GRCh38.p7 | 2:105827882 | ATGATGAAATAGTCT[C/T]GATTGGCATGGTGGT | 8440 |
rs12997075 | snp | G/T | 0.0883596 | 0.190715 | intron-variant | NCK2 | GRCh38.p7 | 2:105858014 | TGCATTTGTGTGTGT[G/T]TGTGTTTTGTTTTTT | 8440 |
rs12997253 | snp | C/T | 0.327445 | 0.237702 | intron-variant | NCK2 | GRCh38.p7 | 2:105827960 | TTATACTAATGTCAG[C/T]TTCCTGGTTTCGATA | 8440 |
rs12999097 | snp | A/G | 0.336017 | 0.234736 | intron-variant | NCK2 | GRCh38.p7 | 2:105892747 | GGTACTCGGGAGGCC[A/G]AGACAGGAGAATCGC | 8440 |
rs13000186 | snp | C/T | | | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105744568 | CACCCACCTACCCTG[C/T]CCCCCACCGCCCGCA | 8440 |
rs13002129 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105820828 | TCCTAATGGACAGAA[A/G]GATGGTGTAGTGGGA | 8440 |
rs13002134 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105820838 | CAGAAGGATGGTGTA[A/G]TGGGATAGGAAGGAC | 8440 |
rs13002184 | snp | A/G | 0.492966 | 0.0588865 | intron-variant | NCK2 | GRCh38.p7 | 2:105871599 | CTCCCAGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 8440 |
rs13003975 | snp | A/C | 0.303438 | 0.244222 | intron-variant | NCK2 | GRCh38.p7 | 2:105881193 | TTCTCATGGTAATTA[A/C]AGTTTGTAAGCACTG | 8440 |
rs13003995 | snp | A/C | 0.339656 | 0.233371 | intron-variant | NCK2 | GRCh38.p7 | 2:105763235 | ACCCTGAGGAGGAGT[A/C]CCTAGCCCTCACCAT | 8440 |
rs13005191 | snp | C/G | 0.341235 | 0.232758 | intron-variant | NCK2 | GRCh38.p7 | 2:105751224 | ATATTCCCCATCACC[C/G]ACTCACTCGGTTATC | 8440 |
rs13006963 | snp | C/G | 0.341235 | 0.232758 | intron-variant | NCK2 | GRCh38.p7 | 2:105751397 | CCAGGGTGACTGCAC[C/G]CTGACAGTCAGGTCT | 8440 |
rs13008961 | snp | A/G/T | 0.00398691 | 0.0444912 | intron-variant | NCK2 | GRCh38.p7 | 2:105821718 | ATATTATCTCTAGTC[A/G/T]CAAATGCAGATGTTA | 8440 |
rs13012641 | snp | C/T | 0.346368 | 0.23068 | intron-variant | NCK2 | GRCh38.p7 | 2:105751654 | TAAAGACTCTCTCCA[C/T]TGGGACTGGTTCAGG | 8440 |
rs13017109 | snp | A/C | 0.335559 | 0.234904 | intron-variant | NCK2 | GRCh38.p7 | 2:105755901 | GCTTTTGAATGTTTA[A/C]TTTCCTTCTTTGTAT | 8440 |
rs13022429 | snp | C/T | 0.48 | 0.0979796 | intron-variant | NCK2 | GRCh38.p7 | 2:105770925 | GTTTGTTTGTTTTTG[C/T]TTTTGTTTTTGTTTT | 8440 |
rs13024715 | snp | A/G | 0.4021 | 0.198407 | intron-variant | NCK2 | GRCh38.p7 | 2:105817493 | TTTATGAGAAGACAC[A/G]TTTTCACCTCCAGAG | 8440 |
rs13024874 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105861903 | TGGCCTGGAATTCTt[C/T]cctccctccctccct | 8440 |
rs13025634 | snp | C/T | 0.328148 | 0.237472 | intron-variant | NCK2 | GRCh38.p7 | 2:105824222 | GCAGAATGCCCCGTC[C/T]GTAAATGTCACGTTT | 8440 |
rs13026762 | snp | A/G | 0.301429 | 0.244653 | intron-variant | NCK2 | GRCh38.p7 | 2:105832907 | tttgttttttggaat[A/G]gtttgaaaagaattg | 8440 |
rs13028719 | snp | C/T | 0.337841 | 0.23406 | intron-variant | NCK2 | GRCh38.p7 | 2:105756712 | TTTGTATTGATGTTA[C/T]TGAAGTCCCCTCGTC | 8440 |
rs13029403 | snp | G/T | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105789541 | TTTTGTTACACATAA[G/T]AGAGTTCTTTCTAGT | 8440 |
rs13030743 | snp | C/T | 0.34146 | 0.23267 | intron-variant | NCK2 | GRCh38.p7 | 2:105750387 | TGTCTCCAAATATAG[C/T]CACTTAGGGGTTAGG | 8440 |
rs13031068 | snp | A/G | 0.429987 | 0.173507 | intron-variant | NCK2 | GRCh38.p7 | 2:105838565 | TATTTTATGGCTCCC[A/G]TATGAATAAAAGACC | 8440 |
rs13031598 | snp | C/T | 0.372794 | 0.217765 | intron-variant | NCK2 | GRCh38.p7 | 2:105759742 | CTTTAGTCTCCGTAG[C/T]GCCTCTGATCTGGGA | 8440 |
rs13032105 | snp | A/G | 0.255224 | 0.249945 | intron-variant | NCK2 | GRCh38.p7 | 2:105818424 | CTAGAACTTAAAAGT[A/G]TAATAAAAATATATA | 8440 |
rs13033333 | snp | C/G | 0.341235 | 0.232758 | intron-variant | NCK2 | GRCh38.p7 | 2:105754555 | TCTCTTTCATGCTTT[C/G]CCTCTCATCAGCTGT | 8440 |
rs13033433 | snp | A/G | 0.340784 | 0.232934 | intron-variant | NCK2 | GRCh38.p7 | 2:105768679 | tgagttttttttgaa[A/G]ttttctttttctcat | 8440 |
rs13033515 | snp | C/T | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105818341 | TAAATGACGAGTTAA[C/T]GGGTGCAGCACACCA | 8440 |
rs13034089 | snp | A/G | 0.439918 | 0.162576 | intron-variant | NCK2 | GRCh38.p7 | 2:105769000 | GGGTGTAGGGGGTGC[A/G]GAAAGTTCCCACTCT | 8440 |
rs13034539 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105880937 | accacaggtggctaa[A/T]ttttttttttttttt | 8440 |
rs13384745 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105793958 | GCTTTTTTTCTTTGG[G/T]GTGGTTTGTTTTTAA | 8440 |
rs13385107 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105835369 | tggctggttttatat[A/G]tatatacatatatat | 8440 |
rs13386530 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | NCK2 | GRCh38.p7 | 2:105792049 | GCTCTGCACAGAGCC[A/G]TGGGAACGCTTCCCC | 8440 |
rs13387154 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | NCK2 | GRCh38.p7 | 2:105819532 | AAAGGTCTTGATCGT[C/T]AGTGACATTAGCAGA | 8440 |
rs13388412 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | NCK2 | GRCh38.p7 | 2:105749802 | GGTTACCCTGGAAAG[A/C]CTCCTCAAGTTCAGA | 8440 |
rs13390822 | snp | A/T | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105841931 | ttagaaaatggagtt[A/T]agttgccaggaggca | 8440 |
rs13391283 | snp | A/C | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105881268 | GGAAATCCCGGTAGG[A/C]TAGGGAGTGTGGTGG | 8440 |
rs13392889 | snp | G/T | 0.389903 | 0.207189 | intron-variant | NCK2 | GRCh38.p7 | 2:105799222 | TTTTATGTTTATGTA[G/T]TTGAATTCATCCCTC | 8440 |
rs13396833 | snp | A/G | 0.454302 | 0.144085 | intron-variant | NCK2 | GRCh38.p7 | 2:105848895 | GTTGAAAATCAAGGT[A/G]GGGATGACAGTATTT | 8440 |
rs13401952 | snp | C/T | 0.382473 | 0.212016 | intron-variant | NCK2 | GRCh38.p7 | 2:105789045 | CCTCCTCCCGATGCC[C/T]GCAGCCTCACTTGTG | 8440 |
rs13411829 | snp | C/G | 0.43978 | 0.162738 | intron-variant | NCK2 | GRCh38.p7 | 2:105849645 | CTCTTCAGGAAGTCA[C/G]ACAAGAGGGCTAGGA | 8440 |
rs13414057 | snp | C/T | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105757138 | ATGGCTCATGTAAAT[C/T]TGAACTTCAACAATC | 8440 |
rs13414634 | snp | A/T | 0.382279 | 0.212137 | intron-variant | NCK2 | GRCh38.p7 | 2:105788500 | GAAACTACTGTTATC[A/T]CCATCTCCTCTTGAA | 8440 |
rs13417262 | snp | G/T | 0.38286 | 0.211774 | intron-variant | NCK2 | GRCh38.p7 | 2:105788613 | TACTTATATGTAGGT[G/T]AAATAAGACACTTCT | 8440 |
rs13422406 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NCK2 | GRCh38.p7 | 2:105828351 | CATATTTTTGTTGTT[A/G]TTGTTTTGATATACA | 8440 |
rs13426109 | snp | C/T | 0.307176 | 0.243374 | intron-variant | NCK2 | GRCh38.p7 | 2:105835967 | tattcagttccaaga[C/T]tttttgtgataaata | 8440 |
rs13426303 | snp | C/T | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105836123 | tatggatttcctttt[C/T]tttgttctgttatta | 8440 |
rs13426321 | snp | A/G | 0.437683 | 0.165152 | intron-variant | NCK2 | GRCh38.p7 | 2:105883824 | TAACAGTTTTTTAAT[A/G]GGGGCCTTTCAGGGT | 8440 |
rs13429270 | snp | C/T | 0.430136 | 0.173352 | intron-variant | NCK2 | GRCh38.p7 | 2:105836604 | gagactgtgcattgg[C/T]tccctttgttctagg | 8440 |
rs13429800 | snp | A/G | 0.45889 | 0.13735 | intron-variant | NCK2 | GRCh38.p7 | 2:105824546 | AAGCTAAATGTAACC[A/G]TATCTTCCAACCTGA | 8440 |
rs17020943 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | NCK2 | GRCh38.p7 | 2:105821912 | TGCTTACCAGCCCAC[A/G]TTCCTTCTGCTTCCC | 8440 |
rs17031732 | snp | C/G | 0.43978 | 0.162738 | intron-variant | NCK2 | GRCh38.p7 | 2:105768905 | TCCCAATGAGTTCAT[C/G]ACGTGGAGGCTCCCC | 8440 |
rs17031736 | snp | C/G | 0.293551 | 0.246177 | intron-variant | NCK2 | GRCh38.p7 | 2:105770783 | GAAAATGTATTTCTA[C/G]CCCTTTAAAGTATTT | 8440 |
rs17031751 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | NCK2 | GRCh38.p7 | 2:105780418 | TGGCTCTCTCATTTT[C/T]GTTTGGTATCTGGGT | 8440 |
rs17031770 | snp | A/G | 0.380333 | 0.213338 | intron-variant | NCK2 | GRCh38.p7 | 2:105784734 | CTGGAGGAGCAGTGT[A/G]TCTGTTGAGGTCCAT | 8440 |
rs17031793 | snp | C/T | 0.24134 | 0.24985 | intron-variant | NCK2 | GRCh38.p7 | 2:105796574 | TGTTCAGATCGGCAG[C/T]GTCTGGACTGAGCCT | 8440 |
rs17031813 | snp | A/C | 0.377582 | 0.214995 | intron-variant | NCK2 | GRCh38.p7 | 2:105807419 | AGTTGTTCTTTGTAG[A/C]AATAAAAAGTGCAAA | 8440 |
rs17031815 | snp | C/G | 0.403684 | 0.197183 | intron-variant | NCK2 | GRCh38.p7 | 2:105810149 | AGTGTGGAATTTTAT[C/G]TAAAGCTGTGCTTAA | 8440 |
rs17031832 | snp | G/T | 0.0322114 | 0.122752 | intron-variant | NCK2 | GRCh38.p7 | 2:105822799 | GGAATTTTCGTGAAT[G/T]CTCTTTAATGCCAGG | 8440 |
rs17031838 | snp | C/T | 0.435407 | 0.167703 | intron-variant | NCK2 | GRCh38.p7 | 2:105823903 | TCAAACGCCTTGTTC[C/T]GTGACCTTCCCGTGT | 8440 |
rs17031841 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | NCK2 | GRCh38.p7 | 2:105824591 | ACGTTTTTGTAATAC[A/G]TTGGTCATTTTCCCA | 8440 |
rs17031843 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | NCK2 | GRCh38.p7 | 2:105824632 | ACCACGTCTCGGCGG[C/T]GTGTGCTTAGAACAG | 8440 |
rs17031845 | snp | C/T | 0.031825 | 0.122064 | intron-variant | NCK2 | GRCh38.p7 | 2:105825260 | CATCTGTGCTGTTAA[C/T]GCTGATCTTCCCTAA | 8440 |
rs17031867 | snp | A/T | 0.084728 | 0.187577 | intron-variant | NCK2 | GRCh38.p7 | 2:105852024 | GTTGTATGGGAACTT[A/T]TAATTTTCACGTGTC | 8440 |
rs17031883 | snp | A/G | 0.256061 | 0.249927 | intron-variant | NCK2 | GRCh38.p7 | 2:105862828 | ATTTTCCTGTGCACT[A/G]AAAGAAGCAGACATA | 8440 |
rs17031921 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | NCK2 | GRCh38.p7 | 2:105882376 | GCCCATTCTGTGTAC[A/G]TAGAAGGCCCGAGTG | 8440 |
rs17031922 | snp | G/T | 0.046775 | 0.145601 | intron-variant | NCK2 | GRCh38.p7 | 2:105882467 | CTGGTTTCTGACACC[G/T]CCTTTTGTTGTTTGC | 8440 |
rs17201484 | snp | C/G | 0.499872 | 0.0079862 | intron-variant | NCK2 | GRCh38.p7 | 2:105778352 | CTGTGTTCTAGCCTT[C/G]AGGAAAGAGCTGCTT | 8440 |
rs17208218 | snp | C/T | 0.426047 | 0.177503 | intron-variant | NCK2 | GRCh38.p7 | 2:105789496 | GCCTGGCCTCACAAC[C/T]TTTTTTCAATGAGAA | 8440 |
rs17208505 | snp | A/C | 0.417683 | 0.185425 | intron-variant | NCK2 | GRCh38.p7 | 2:105798772 | GCAGTAGCTGTGGTT[A/C]TTCATAGATAAATAC | 8440 |
rs17210439 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | NCK2 | GRCh38.p7 | 2:105867134 | TGTAACATAAGGGGA[A/T]GAAAATTCAGCTATC | 8440 |
rs17267584 | snp | C/T | 0.0562307 | 0.157967 | intron-variant | NCK2 | GRCh38.p7 | 2:105781760 | CTGTGACAGAGCTGT[C/T]GCCTCTCCGCAGTAC | 8440 |
rs17269688 | snp | A/G | 0.0887219 | 0.191022 | intron-variant | NCK2 | GRCh38.p7 | 2:105852811 | GTTAGTGAGTTCTAC[A/G]TGGTATGCACTTGAG | 8440 |
rs17663742 | snp | A/G | 0.029116 | 0.117091 | intron-variant | NCK2 | GRCh38.p7 | 2:105883117 | TTTATGGTGTCATCA[A/G]TTTTGCGGAGCCTTA | 8440 |
rs28758995 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105807817 | TCCCTTCTATCTCTC[C/T]CTCCCTCCCTCCCTT | 8440 |
rs33913336 | in-del | -/CCC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105812790 | CTGCTCATTACTGAA[-/CCC]GCCAGGTGACACTAT | 8440 |
rs33961225 | in-del | -/AAAG | | | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893736 | GCTGTGCTTGCAATA[-/AAAG]AAGAATTTCCTGGAA | 8440 |
rs34000199 | snp | A/G | 0.00147929 | 0.0271561 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881887 | TGGGGCGTGCGCAGG[A/G]TGCAGGGCAGGCCCG | 8440 |
rs34049215 | in-del | -/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105748696 | TACTGGGATTACAGG[-/G]CCAGAGCCACCATAC | 8440 |
rs34055721 | in-del | -/A | | | intron-variant | NCK2 | GRCh38.p7 | 2:105827643 | TTCAAAGCATTGAAA[-/A]TCATACAGAGTGTCT | 8440 |
rs34066246 | in-del | -/A | | | intron-variant | NCK2 | GRCh38.p7 | 2:105758441 | TTGAGACAGAGTCTC[-/A]GCTCTGTCACCCATG | 8440 |
rs34088457 | in-del | -/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105769548 | CAGAAGAATAACTCC[-/C]ACAGTAGAAGTTAGG | 8440 |
rs34094619 | in-del | -/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105767594 | ATCTGTGGCTGCCCC[-/C]ATGTTGCAACAGCAG | 8440 |
rs34108779 | in-del | -/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105877379 | TGGGCAGGATCAGGG[-/G]TGCAGGGAGGAGAAG | 8440 |
rs34110097 | snp | C/T | 0.343477 | 0.231866 | intron-variant | NCK2 | GRCh38.p7 | 2:105755472 | AGCCGATTCCGTCTT[C/T]CATAAGAAGTAGGTT | 8440 |
rs34206399 | in-del | -/A | | | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105851344 | CTCGGCTCACTGCAA[-/A]CATCCGCCTCCCGGG | 8440 |
rs34235939 | in-del | -/A | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105892861 | AAAAAAAAAAAAAAA[-/A]GCAGAGACCCAGTGT | 8440 |
rs34261181 | snp | C/T | 0.330016 | 0.236849 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771533 | TTGGGCCACTGTACT[C/T]CAGCCTGGGCGACAA | 8440 |
rs34320453 | in-del | -/A | 0.429087 | 0.174436 | intron-variant | NCK2 | GRCh38.p7 | 2:105841716 | TGCCTAGGGGCTGCC[-/A]AGCCACCAGTCACCT | 8440 |
rs34322266 | in-del | -/A | | | intron-variant | NCK2 | GRCh38.p7 | 2:105759849 | CTGTCCCTCAGTTGA[-/A]GAGTTGTCAGATGTT | 8440 |
rs34334707 | in-del | -/TGAA | | | intron-variant | NCK2 | GRCh38.p7 | 2:105757952 | CACCACAGCTGGGGT[-/TGAA]GAAGCACCTCTATTC | 8440 |
rs34347764 | in-del | -/C | | | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893818 | AATTTACCCCAAATG[-/C]TGCCATCCACATAGT | 8440 |
rs34380678 | in-del | -/C | | | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105743170 | TGATGGTGTTTCAGG[-/C]AAATAGCAGAAATGC | 8440 |
rs34393156 | in-del | -/A | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105846488 | CACTGAAAAAAAAAA[-/A]TAATAGGAGGGTGTA | 8440 |
rs34406938 | in-del | -/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105777441 | GGAATGAAATGACCC[-/C]AGTGCTCACCACCTG | 8440 |
rs34415670 | in-del | -/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105822180 | GCAGTTTGGAGAGTT[-/C]CTTTGGAAACGTAAG | 8440 |
rs34425192 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105874972 | CCAAGTCAGCTATTT[-/T]GCCACTTAAAATTAT | 8440 |
rs34434093 | in-del | -/A | | | intron-variant | NCK2 | GRCh38.p7 | 2:105837261 | TCTTAATGACGTCAA[-/A]GCTCCTTGATTTTTA | 8440 |
rs34445543 | in-del | -/TTT | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105855850 | TTTTTTTTTTTTTTT[-/TTT]GAGACGGAGTCTCAC | 8440 |
rs34519484 | in-del | -/TT | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105774026 | TTTTTTTTTTTTTTT[-/TT]GAGACGGAGTCTCGC | 8440 |
rs34530540 | snp | C/T | 0.40157 | 0.198813 | intron-variant | NCK2 | GRCh38.p7 | 2:105817938 | TACTGGGTATATACC[C/T]AAAGGAATATAAATC | 8440 |
rs34536881 | in-del | -/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105760131 | GTACCTCCTGTAGGG[-/G]TTGTATTTACATTAG | 8440 |
rs34541978 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105768510 | CCCATGACCTCACTT[-/T]CAGGTTCCATAATTT | 8440 |
rs34554853 | snp | A/G | 0.434109 | 0.169127 | intron-variant | NCK2 | GRCh38.p7 | 2:105832475 | CTGTCGTTAAGGCTC[A/G]TATTACCTAATTTGT | 8440 |
rs34565455 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | NCK2 | GRCh38.p7 | 2:105819602 | GCAGGGGAGTGTGGC[A/G]TGCTCACCCAGCAGC | 8440 |
rs34570599 | in-del | -/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105859390 | CTCACCCTGCCACCC[-/C]TACCTACCTGGGACT | 8440 |
rs34596947 | snp | A/G | 0.324382 | 0.238678 | intron-variant | NCK2 | GRCh38.p7 | 2:105814693 | CTCCAGTCGGTTGGG[A/G]AAAACCTTTAGTGTC | 8440 |
rs34629499 | in-del | -/A | 0.499999 | 0.000599041 | intron-variant | NCK2 | GRCh38.p7 | 2:105799270 | GTTTAAAAAAAAAAA[-/A]GTTCTTCCTTCAGGG | 8440 |
rs34631040 | in-del | -/T | 0.438806 | 0.163867 | intron-variant | NCK2 | GRCh38.p7 | 2:105838102 | GTCCTTTTTTTTTTT[-/T]GTACCAGCAATAGAT | 8440 |
rs34641961 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105873899 | GGCCATGTCCTCCTA[C/G]GGACGGTATTTCCCC | 8440 |
rs34675021 | in-del | -/A | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105765991 | CAGCAGGTGACGCTT[-/A]ACACTGCACAGGTAT | 8440 |
rs34683197 | in-del | -/GTGT/GTGTGT/GTGTGTGT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105823173 | TGTGTGTGTGTGTGT[-/GTGT/GTGTGT/GTGTGTGT]CACAATGGAGGGGGT | 8440 |
rs34710147 | in-del | -/A | | | intron-variant | NCK2 | GRCh38.p7 | 2:105781696 | AGCAATGCATGAAAA[-/A]GTACAGAGCCTGTGG | 8440 |
rs34712037 | in-del | -/A | 0.499996 | 0.00139776 | intron-variant | NCK2 | GRCh38.p7 | 2:105782684 | ATCGTTTCTGAGAGT[-/A]GGGGGATCCGGCCCG | 8440 |
rs34721498 | in-del | -/T | 0.451359 | 0.148171 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105772896 | TCCCACGTGTCCACA[-/T]TTTTTTTTTTTTTTT | 8440 |
rs34723967 | in-del | -/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105755272 | TGGTGGCATTATCAT[-/G]CTTTTTTAAAAAAGG | 8440 |
rs34727686 | in-del | -/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105824771 | GTAGATGAAGTTGGG[-/G]TGTGTGAACTTGGAA | 8440 |
rs34753086 | in-del | -/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105761627 | CATGCCTGTAATCCC[-/C]AGCACTTTGGGAGGC | 8440 |
rs34797552 | in-del | -/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105803587 | AAGTGCGGAACTGGC[-/C]ATTAGCATCCAGTTT | 8440 |
rs34806039 | in-del | -/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105801309 | GACGTCATTGTAGGG[-/G]ATCCCCCAGCCCCAG | 8440 |
rs34865216 | snp | C/T | 0.34146 | 0.23267 | intron-variant | NCK2 | GRCh38.p7 | 2:105753662 | CTTCCAAGTGGCCCC[C/T]GGACTTTTGTGCTGT | 8440 |
rs34871017 | in-del | -/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105799576 | AGTCTGTCTATCTGC[-/C]ACACCAAACACGAGC | 8440 |
rs34872603 | in-del | -/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105834750 | TAGCTCCCTGTAGCC[-/C]TTGAACTGTTGGGTT | 8440 |
rs34892176 | snp | A/G | 0.328616 | 0.237317 | intron-variant | NCK2 | GRCh38.p7 | 2:105773927 | AAGACAAAACCCTCT[A/G]TTTATAAGAAAGATG | 8440 |
rs35013458 | in-del | -/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105884325 | GCTTTCGCAGCCACC[-/C]ACTAGGCCACCAAGA | 8440 |
rs35034760 | snp | C/T | 0.365439 | 0.221752 | intron-variant | NCK2 | GRCh38.p7 | 2:105816036 | CCCCAACCCGAGTGT[C/T]GGAGCTTGCCCAGGG | 8440 |
rs35044148 | in-del | -/T | 0.487049 | 0.0794222 | intron-variant | NCK2 | GRCh38.p7 | 2:105861514 | TTTTTTTTTTTTTTT[-/T]GAGACGGTGTCTTGC | 8440 |
rs35048252 | snp | C/T | 0.327211 | 0.237778 | intron-variant | NCK2 | GRCh38.p7 | 2:105827062 | TGGAGTGCAGTGGCA[C/T]GATCTCGGCTCACTG | 8440 |
rs35058827 | in-del | -/T | 0.499824 | 0.00938333 | intron-variant | NCK2 | GRCh38.p7 | 2:105769797 | GGTCAGTAAAAGGAG[-/T]TGTAGAAGGTAAACC | 8440 |
rs35071469 | in-del | -/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105783763 | CTCTTTCCAAGAGGG[-/G]TGGCCTGTTCCTGAG | 8440 |
rs35114253 | in-del | -/G | 0.305685 | 0.24372 | intron-variant | NCK2 | GRCh38.p7 | 2:105842324 | CTCCTGACCTCAGGT[-/G]ATCTACCTGCCTCAG | 8440 |
rs35115960 | in-del | -/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105873756 | GCTCAGATGATTGGG[-/G]AAGTACGATTGGATC | 8440 |
rs35118881 | in-del | -/G | 0.4021 | 0.198407 | intron-variant | NCK2 | GRCh38.p7 | 2:105816068 | TGAAAGGTGGGAAGA[-/G]GGGAGTACATGTGTG | 8440 |
rs35132021 | in-del | -/A | 0.406123 | 0.195258 | intron-variant | NCK2 | GRCh38.p7 | 2:105819918 | ACTGTTGTAGCAGTT[-/A]AAAAAAAAATAGATA | 8440 |
rs35133141 | in-del | -/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105816835 | GGATGGTAGACACCT[-/G]ACAACCTGTAAGATG | 8440 |
rs35133660 | in-del | -/G/T | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105833673 | TTTTTGCATTTTTTT[-/G/T]GGCCTCTTTTGTTCA | 8440 |
rs35152135 | in-del | -/T | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105794065 | TTTTTTTTTTTTTTT[-/T]GGAGACGGAATCTTG | 8440 |
rs35168059 | snp | A/G | 0.440195 | 0.162252 | intron-variant | NCK2 | GRCh38.p7 | 2:105768512 | CCATGACCTCACTTC[A/G]GGTTCCATAATTTGC | 8440 |
rs35190076 | in-del | -/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105776544 | GCTGCCAGCCTTGGG[-/G]TTGTCCCCTGGCCTG | 8440 |
rs35198980 | in-del | -/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105870149 | TTGGAAGACACTCGG[-/G]CCCCACCTGTATGGG | 8440 |
rs35201475 | snp | G/T | 0.4021 | 0.198407 | intron-variant | NCK2 | GRCh38.p7 | 2:105817819 | AATAGGAACACTTTT[G/T]CACTGTTGGTGGGAC | 8440 |
rs35255417 | in-del | -/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105841173 | TGTAGATTTACTGGG[-/G]CACTAACCAAAGTCT | 8440 |
rs35264290 | snp | A/G | 0.337386 | 0.23423 | intron-variant | NCK2 | GRCh38.p7 | 2:105751731 | TGGAACTGAGCATGG[A/G]CCCAGCTCTCTGTCA | 8440 |
rs35266897 | in-del | -/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105767286 | GCTCGTGACGTGGCC[-/C]TACTTGGATGTCTGA | 8440 |
rs35279449 | in-del | -/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105874048 | AGGAATTTTGTTTGA[-/C]TAAGAGAAGGGACAA | 8440 |
rs35318143 | in-del | -/CT | 0.436265 | 0.166749 | intron-variant | NCK2 | GRCh38.p7 | 2:105892497 | TTTCAGAATCGTGGA[-/CT]CTACCTCCAGGTCTT | 8440 |
rs35388938 | in-del | -/A | | | intron-variant | NCK2 | GRCh38.p7 | 2:105860410 | TCCCAGAGGTCAGGA[-/A]TGGACAGAGCCCCTG | 8440 |
rs35443139 | snp | C/G | 0.393434 | 0.20476 | intron-variant | NCK2 | GRCh38.p7 | 2:105765803 | TGTGTGTGTGTGTGT[C/G]TGTGTGTGTGTGTCT | 8440 |
rs35482041 | snp | A/G | 0.332337 | 0.236052 | intron-variant | NCK2 | GRCh38.p7 | 2:105792979 | TTCCCTTTCTCACCA[A/G]CCGAGTCAGCTTTTC | 8440 |
rs35497405 | in-del | -/A | 0.37138 | 0.218556 | intron-variant | NCK2 | GRCh38.p7 | 2:105819344 | AACTCCGTTTTCTTT[-/A]AAAAAAAAAAAAAAA | 8440 |
rs35540843 | in-del | -/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105872887 | CTCCTTCATCCGGGG[-/G]ACACCTCTGTTGAGC | 8440 |
rs35548171 | in-del | -/GCCTTAG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105786857 | CTGCTCCCACCCTAG[-/GCCTTAG]CCTTAGGCTGACTCC | 8440 |
rs35571182 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105885312 | TACAGTACTTTTTTT[-/T]CCAGTAGAGAAAAAC | 8440 |
rs35611917 | snp | A/G | 0.308166 | 0.243139 | intron-variant | NCK2 | GRCh38.p7 | 2:105858392 | AGTATCTGGGACTAC[A/G]GGCATGCACTACCAC | 8440 |
rs35613364 | in-del | -/A | | | intron-variant | NCK2 | GRCh38.p7 | 2:105791749 | GCTTGTGAGTTTTGT[-/A]CTATAATTTGATCCA | 8440 |
rs35622044 | snp | A/G | 0.375598 | 0.21616 | intron-variant | NCK2 | GRCh38.p7 | 2:105787638 | GAGCTGACTCAGGCA[A/G]TGAAGCTACCTCAGT | 8440 |
rs35665139 | in-del | -/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105862624 | ATGAGAAACCTCGGG[-/G]AGTAACTAGCAAGCC | 8440 |
rs35666580 | snp | C/T | 0.341235 | 0.232758 | intron-variant | NCK2 | GRCh38.p7 | 2:105753330 | CATCACTGAGGACCA[C/T]TGGCCTGGCTGCTCC | 8440 |
rs35666819 | in-del | -/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105793462 | TGACCTCGGGCATCC[-/C]TGTTTCTGAGACAAG | 8440 |
rs35671530 | in-del | -/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105812338 | ATCAGTCCACATGGG[-/G]TTGAACTTTGGCCAA | 8440 |
rs35677272 | snp | C/T | 0.436408 | 0.16659 | intron-variant | NCK2 | GRCh38.p7 | 2:105892746 | AGGTACTCGGGAGGC[C/T]GAGACAGGAGAATCG | 8440 |
rs35678376 | snp | A/G | 0.0174175 | 0.0916809 | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105744208 | TGGCCTGGATGCCTG[A/G]GAGGCAACAGAGGTC | 8440 |
rs35681920 | in-del | -/G | | | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105772384 | GAACCTAGAAAAAGG[-/G]AAAATGTTCCTTTCT | 8440 |
rs35812588 | snp | C/T | 0.413083 | 0.189483 | intron-variant | NCK2 | GRCh38.p7 | 2:105815744 | TTGGTGGCTTCTCAA[C/T]AAATGGCTGGTGCAA | 8440 |
rs35817451 | snp | A/G | 0.0113386 | 0.0744361 | synonymous-codon | NCK2 | GRCh38.p7 | 2:105855264 | CTTCAGGTTCTTCAC[A/G]AGGGAGCCCTTCTTC | 8440 |
rs35817953 | in-del | -/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105823914 | TTCCGTGACCTTCCC[-/C]GTGTGAAGGTCTACC | 8440 |
rs35820275 | in-del | -/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105812569 | CTCTGCTGGGCCTCC[-/C]TTGGTCAGGGAGGGA | 8440 |
rs35823954 | in-del | -/A | 0.364193 | 0.222396 | intron-variant | NCK2 | GRCh38.p7 | 2:105806837 | GTAATTTACAAAATT[-/A]AAAAAAAACCCAACC | 8440 |
rs35833326 | in-del | -/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105809609 | TTATGAAGTACTGGG[-/G]TGTTGAGACTTCAAC | 8440 |
rs35853228 | snp | G/T | 0.417845 | 0.185278 | intron-variant | NCK2 | GRCh38.p7 | 2:105765786 | CAGCTTAGAATAGGG[G/T]GTGTGTGTGTGTGTG | 8440 |
rs35866817 | snp | C/T | 0.364817 | 0.222075 | intron-variant | NCK2 | GRCh38.p7 | 2:105786112 | TAATTAATCCATTCA[C/T]CCAGCCAGCCTTTTA | 8440 |
rs35868906 | in-del | -/T | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105889592 | GAGAATTTGCATTTC[-/T]TTTTTTTTTTTTTTT | 8440 |
rs35931398 | in-del | -/T | 0.0788843 | 0.182262 | intron-variant | NCK2 | GRCh38.p7 | 2:105834652 | ATTTACATTAAAGGG[-/T]TTTTTTTTCAATTTT | 8440 |
rs35937108 | in-del | -/G | | | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105851334 | GTGGCGCGATCTCGG[-/G]CTCACTGCAACATCC | 8440 |
rs35954499 | in-del | -/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105756722 | GTTACTGAAGTCCCC[-/C]TCGTCCCTCAAAACA | 8440 |
rs35962114 | in-del | -/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105765046 | TTTAGTGTAAATTCC[-/C]TTGGAGAGGCATTGC | 8440 |
rs36163547 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105835285 | AATTCCTCCAATTTT[-/T]GCTTGTCTGGGAAAG | 8440 |
rs55652532 | in-del | -/C | 0.429238 | 0.174281 | intron-variant | NCK2 | GRCh38.p7 | 2:105756345 | GTACAATCAATCTTT[-/C]CCTTTCTTCAGTCAT | 8440 |
rs55681756 | snp | C/T | 0.236094 | 0.249613 | intron-variant | NCK2 | GRCh38.p7 | 2:105884238 | CTTTGCTTGTTTTTT[C/T]CCCACCATCCACTGC | 8440 |
rs55708648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105782796 | GTTAGGCTTGTGCTC[A/G]GCTCTGGCAGCCACA | 8440 |
rs55741072 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105835396 | ATATACACATATATA[C/T]ATATATATACGTGTA | 8440 |
rs55760016 | snp | A/G | 0.021333 | 0.101051 | intron-variant | NCK2 | GRCh38.p7 | 2:105802130 | TGCATGGTTAGAGCA[A/G]TGGGGACCATCTGGG | 8440 |
rs55830542 | snp | C/T | 0.499809 | 0.00978247 | intron-variant | NCK2 | GRCh38.p7 | 2:105770749 | AGATCTTTAACAGGT[C/T]AAGAAAAATAATACT | 8440 |
rs55903032 | in-del | -/GT/GTATATATATATAT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105835388 | TACATATATATACAC[-/GT/GTATATATATATAT]ATATATATATATATA | 8440 |
rs55909865 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105885777 | AACCATTTCTGCATA[A/C]TACTACATTTCCATG | 8440 |
rs55938757 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105780798 | GCATGTGAGGACACA[A/G]CAAGAAGCCGCCGTG | 8440 |
rs55991015 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105772020 | GAACTCTTCAGCTCT[G/T]AGTCTTTGAGAACTC | 8440 |
rs56014876 | in-del | -/ACACACACAC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105864865 | CACACACACACACAC[-/ACACACACAC]GGTTCCCTGCAAATG | 8440 |
rs56041518 | snp | A/C/G | 0.021333 | 0.101051 | intron-variant | NCK2 | GRCh38.p7 | 2:105789934 | CAACTAAATGTTCAC[A/C/G]AATGGATGTTGTGTT | 8440 |
rs56051993 | snp | C/T | 0.0861826 | 0.188849 | intron-variant | NCK2 | GRCh38.p7 | 2:105757569 | CAGTTCATACCTACA[C/T]AGGACCAGCCATGGG | 8440 |
rs56052516 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105835375 | GTTTTATATATATAT[A/G]CATATATATACACAT | 8440 |
rs56102314 | snp | A/T | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105764878 | TTTTCAAATCCTTTT[A/T]TTCCATGTTGTGTGA | 8440 |
rs56105127 | snp | C/T | 0.304438 | 0.244001 | intron-variant | NCK2 | GRCh38.p7 | 2:105845479 | ACTCACTGCATCCTC[C/T]GCCTCTTGAGCTCAA | 8440 |
rs56119132 | snp | A/G | 0.257176 | 0.249897 | intron-variant | NCK2 | GRCh38.p7 | 2:105794330 | GTGCTAGGATTACAG[A/G]CATGCGCCACCATGC | 8440 |
rs56124558 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105873320 | GGCCCACCCTAAGTC[A/C]ACTCTGAGAGCCCCC | 8440 |
rs56131463 | snp | C/T | 0.137867 | 0.223442 | intron-variant | NCK2 | GRCh38.p7 | 2:105746706 | TTGGAACAGGGGTTT[C/T]CTGAGAAGCAAGTGT | 8440 |
rs56141591 | in-del | -/TTTTTTTTT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105806247 | TTCTTTCTTTTTTTT[-/TTTTTTTTT]GAGACAGAGTCTCAC | 8440 |
rs56167725 | in-del | -/GTGTGTGTGTGTGTGT | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105823158 | TGTGTGTGTGTGTGT[-/GTGTGTGTGTGTGTGT]CACAATGGAGGGGGT | 8440 |
rs56209615 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105809178 | CAAAGTGTGGGTCAC[A/C]TGGTGGTTTTGACCT | 8440 |
rs56217624 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NCK2 | GRCh38.p7 | 2:105859245 | GCCTTGCAAAGCCCC[A/G]AAGGTTAATTCTCTT | 8440 |
rs56219046 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105797020 | AAGCATAGTCTTGCA[A/G]AAATGGATTTAGTCA | 8440 |
rs56220635 | in-del | -/GTGT | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105830713 | TGTGTGTGTGTGTGT[-/GTGT]TTGGTCTGATAATAC | 8440 |
rs56247904 | in-del | -/T/TT | 0.625 | 0.125 | intron-variant | NCK2 | GRCh38.p7 | 2:105831424 | CTTTTTTTTTTTTTT[-/T/TT]GTCTTTTTGATAATA | 8440 |
rs56250020 | in-del | -/GTATATATATATACGTAT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105835410 | TATATATATACGTGT[-/GTATATATATATACGTAT]ATATATATATATATT | 8440 |
rs56307960 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NCK2 | GRCh38.p7 | 2:105827245 | ACCTCGTGATCTACC[C/T]GCCTTGGCCTCCCAA | 8440 |
rs56344443 | in-del | -/A | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105846478 | GGTAGATACTCACTG[-/A]AAAAAAAAAAATAAT | 8440 |
rs56346816 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105820264 | GCCATTTGGTCGGTG[A/G]TCCTTGAAGTGCCAA | 8440 |
rs56347611 | in-del | -/TT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105758428 | TTTTTTTTTTTTTTT[-/TT]GAGACAGAGTCTCGC | 8440 |
rs56679403 | in-del | -/TTT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105889592 | TTTTTTTTTTTTTTT[-/TTT]AATTATTTTGAGATA | 8440 |
rs56917992 | in-del | -/GT/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105765786 | TGTGTGTGTGTGTGT[-/GT/T]CTGTGTGTGTGTGTG | 8440 |
rs57005277 | in-del | -/ATTACACATA/TT/TTACACATAA | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105759473 | GGCTTTTATATAATA[-/ATTACACATA/TT/TTACACATAA]AAACATATGGTATAT | 8440 |
rs57084125 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105820389 | GCCTTGGATGCATTT[C/T]CCAGTTATTGGACAC | 8440 |
rs57276187 | in-del | -/ACACACACACACACACACAC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105864855 | CACACACACACACAC[-/ACACACACACACACACACAC]GGTTCCCTGCAAATG | 8440 |
rs57296433 | in-del | -/ACAC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105864871 | CACACACACACACAC[-/ACAC]GGTTCCCTGCAAATG | 8440 |
rs57338911 | in-del | -/C | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105883059 | CGACTGGGATGTGCT[-/C]CTCTTTGAGGACGGA | 8440 |
rs57402702 | snp | A/G | 0.40263 | 0.198 | intron-variant | NCK2 | GRCh38.p7 | 2:105833269 | CTGGCTAATTCTTTT[A/G]TACTTTTACTAGAGA | 8440 |
rs57437485 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105749098 | ACAAAGCCAACCCCA[A/T]ACTCAACTGTATTAC | 8440 |
rs57534584 | in-del | -/TATC | 0.341235 | 0.232758 | intron-variant | NCK2 | GRCh38.p7 | 2:105752395 | TTCAGTTAAAACTAA[-/TATC]TATCATCAAAATACC | 8440 |
rs57567085 | snp | C/G | 0.137867 | 0.223442 | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105744260 | AGTGCCTCGGACAGG[C/G]ATGATGGACTAAAAA | 8440 |
rs57572811 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105745807 | CCACCTGAATGAACC[A/G]AAGTTTCTCACAATC | 8440 |
rs57691358 | in-del | -/TTC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105868725 | GTTTTCTTTTTCTTC[-/TTC]AAAGCCTGCTATACA | 8440 |
rs57747666 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | NCK2 | GRCh38.p7 | 2:105853017 | TTTTTTTAGCATCTA[G/T]TAGAAAATATGTTAT | 8440 |
rs57857814 | in-del | -/CACACACACACA | | | intron-variant | NCK2 | GRCh38.p7 | 2:105780364 | ACACACACACACACA[-/CACACACACACA]TTCATCTAAAGGACA | 8440 |
rs57930309 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | NCK2 | GRCh38.p7 | 2:105832654 | GAATGTGTCCCACTT[A/G]ATCATGGTGTATTGT | 8440 |
rs58080376 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105892047 | AAATGCTTAGAATTA[G/T]AAAAATTAGCCAGGC | 8440 |
rs58094004 | in-del | -/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105844577 | GTAGAAAAAAACAAA[-/C]AAAAAAAAAAAACAG | 8440 |
rs58169414 | in-del | -/AC/ATATATATATATATATATATATATACATAC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105835408 | TATATATATATACGT[lengthTooLong]GTATATATATATATA | 8440 |
rs58195928 | snp | G/T | 0.402277 | 0.198272 | intron-variant | NCK2 | GRCh38.p7 | 2:105810312 | GAAAAAAACAAAAGT[G/T]TGTGTGTGTGAGAGA | 8440 |
rs58421301 | snp | C/T | 0.0850919 | 0.187897 | intron-variant | NCK2 | GRCh38.p7 | 2:105848110 | GTGATGACTGGGCAT[C/T]ACGTGGACATTAGCA | 8440 |
rs58483160 | in-del | -/T | 0.377904 | 0.214804 | intron-variant | NCK2 | GRCh38.p7 | 2:105795303 | GTGATATATTTTTAA[-/T]TTTTTTTTTCCTCAA | 8440 |
rs58533035 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | NCK2 | GRCh38.p7 | 2:105800156 | TAGCCTGGCTGCACC[A/G]TATAGTCTGGCTCTC | 8440 |
rs58557425 | in-del | -/CATATATATATATGTATGTATATATATGTATATA | | | intron-variant | NCK2 | GRCh38.p7 | 2:105835399 | ACACATATATATATA[lengthTooLong]TATATACGTGTATAT | 8440 |
rs58568265 | snp | C/G | 0.0733688 | 0.176922 | intron-variant | NCK2 | GRCh38.p7 | 2:105802880 | GCCACCCAGTTGTCT[C/G]TTTCATCTGCTGCTT | 8440 |
rs58581494 | snp | G/T | 0.0905309 | 0.192535 | intron-variant | NCK2 | GRCh38.p7 | 2:105880721 | GGATGCTCTAAAAAT[G/T]GTTATTTCAGAAGGA | 8440 |
rs58592956 | in-del | -/A | 0.351853 | 0.228311 | intron-variant | NCK2 | GRCh38.p7 | 2:105806710 | GCTACTTAATGAGGG[-/A]AAAAAAATCACGTTG | 8440 |
rs58597816 | snp | A/G | 0.396546 | 0.202545 | intron-variant | NCK2 | GRCh38.p7 | 2:105811734 | TCTCCTGTCCAGCCC[A/G]CTGCCACTGGACTCT | 8440 |
rs58699924 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105806238 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTCAC | 8440 |
rs58744207 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105765785 | CAGCTTAGAATAGGG[-/T]GGTGTGTGTGTGTGT | 8440 |
rs58927672 | snp | A/G | 0.081446 | 0.184634 | intron-variant | NCK2 | GRCh38.p7 | 2:105810278 | CTCACCTTCTGGCCC[A/G]CTTCTTAAGATGCTA | 8440 |
rs58931849 | snp | A/G | 0.499801 | 0.00998203 | intron-variant | NCK2 | GRCh38.p7 | 2:105770946 | TTTTTGTTTTGAGAC[A/G]GAGTCTCGCTCTGTC | 8440 |
rs58932690 | in-del | -/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105885301 | TTTTTTGTCATACAG[-/G]TACTTTTTTTTCCAG | 8440 |
rs59005322 | in-del | -/TTTTTTTTTTTTT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105880956 | TTTTTTTTTTTTTTT[-/TTTTTTTTTTTTT]GCAGACACGGTCTCG | 8440 |
rs59154186 | in-del | -/ATATTT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105835424 | TATATATATATATAT[-/ATATTT]TTTTTTTTTGGTCAG | 8440 |
rs59155187 | in-del | -/ATGTGTGTGTGTGTGTGT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105830710 | TGTGTGTGTGTGTGT[-/ATGTGTGTGTGTGTGTGT]GTGTGTTTGGTCTGA | 8440 |
rs59432417 | in-del | -/CTTTTG | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105770925 | GTTTGTTTGTTTTTG[-/CTTTTG]TTTTTGTTTTGAGAC | 8440 |
rs59435090 | snp | C/T | 0.258843 | 0.249844 | intron-variant | NCK2 | GRCh38.p7 | 2:105787906 | GCGTATACCGCCCCC[C/T]ACCGCCCCCGACTTG | 8440 |
rs59704520 | in-del | -/G | 0.0391693 | 0.134352 | intron-variant | NCK2 | GRCh38.p7 | 2:105873672 | TTTTATTTTTTGGGG[-/G]CTCTTAATTGAAGAG | 8440 |
rs59731130 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105857048 | TTTTTTTTTTTTTTT[A/T]TGTATTTACAAGATT | 8440 |
rs59901042 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | NCK2 | GRCh38.p7 | 2:105764916 | TGGAGTTGAAAGCGC[C/T]ACACTTGCATAAGTA | 8440 |
rs59912414 | snp | A/C | 0.301429 | 0.244653 | intron-variant | NCK2 | GRCh38.p7 | 2:105833218 | TCCTGCCTCAATCTC[A/C]CGAGTAGCTGGGATT | 8440 |
rs60064271 | in-del | -/GTGTGTGT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105823166 | TGTGTGTGTGTGTGT[-/GTGTGTGT]CACAATGGAGGGGGT | 8440 |
rs60083036 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105835373 | TGGTTTTATATATAT[A/G]TACATATATATACAC | 8440 |
rs60133553 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105891573 | TTTTTTTTTTTGAGA[G/T]TTTTCGCTCTTGTTG | 8440 |
rs60227000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105781404 | AAGACTTGACTAAAT[A/G]CAATCTCCCTTTTGA | 8440 |
rs60247922 | snp | A/G | 0.021333 | 0.101051 | intron-variant | NCK2 | GRCh38.p7 | 2:105801936 | CAGCTCAGGCTGCAG[A/G]CCCATCTCCCTGCAT | 8440 |
rs60258894 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105882164 | GAAAGAGCGGGAGAC[C/G]CAGATGAATGCAATT | 8440 |
rs60398425 | snp | A/C | 0.0260105 | 0.111035 | intron-variant | NCK2 | GRCh38.p7 | 2:105784154 | TGTCACCCAGGCTGG[A/C]GTGCAGTGGCGTCAT | 8440 |
rs60438850 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105789930 | CGCCAACTAAATGTT[-/T]CACGAATGGATGTTG | 8440 |
rs60490215 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | NCK2 | GRCh38.p7 | 2:105837849 | TGAGTTATTTTTATG[C/T]TTATTCACCATTTGT | 8440 |
rs60524274 | snp | C/T | 0.039522 | 0.134904 | intron-variant | NCK2 | GRCh38.p7 | 2:105855897 | TGGAGTGCAGTGGCA[C/T]GATCTTGCCTCACTG | 8440 |
rs60569363 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105874731 | TCTGTTACAACATCT[C/T]TTCATCTGAAAGGGG | 8440 |
rs60670971 | in-del | -/T | 0.448066 | 0.152544 | intron-variant | NCK2 | GRCh38.p7 | 2:105832847 | AAGAATTCTCTTCTC[-/T]TTTTTTTTTTTATTT | 8440 |
rs60947847 | in-del | -/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105833675 | TTTGCATTTTTTTGG[-/G]CCTCTTTTGTTCAGT | 8440 |
rs61091716 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | NCK2 | GRCh38.p7 | 2:105800636 | ACAAGAAACATTCAT[C/T]CTGTTTTTGGTCTGT | 8440 |
rs61207411 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | NCK2 | GRCh38.p7 | 2:105877307 | ACATTAAATCTTCAT[A/T]TGCCAGCATTCAGGA | 8440 |
rs61245337 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105811074 | CAGCTACTCGGGAGG[C/T]TGAGGTAAGAGAATC | 8440 |
rs61289904 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105832111 | TTCTTAGGTATTTGG[C/G]TTTTTTTCTTTTATT | 8440 |
rs61292600 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | NCK2 | GRCh38.p7 | 2:105831521 | AGTAGGTTTATAGTT[G/T]GGGGGCTTACATTTA | 8440 |
rs61440392 | in-del | -/A/ATT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105865930 | ATTATTATTATTATT[-/A/ATT]TGAGACAGAGTTTCA | 8440 |
rs61478863 | in-del | -/GATTA | | | intron-variant | NCK2 | GRCh38.p7 | 2:105770824 | AGTCATTTTGGGTTA[-/GATTA]AACAGTTTGGCATTT | 8440 |
rs62148192 | snp | A/C | 0.0271762 | 0.113356 | intron-variant | NCK2 | GRCh38.p7 | 2:105871017 | TCTGCTCATCGTGAT[A/C]CTGGCCTCCTACTTT | 8440 |
rs62148193 | snp | A/G | 0.107076 | 0.205424 | intron-variant | NCK2 | GRCh38.p7 | 2:105892076 | GCATGGTGGCACATC[A/G]GGAGGCTGAGGCAGG | 8440 |
rs62148194 | snp | C/T | 0.105924 | 0.204309 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893728 | GCCTTTGGGGCTGTG[C/T]TTGCAATAAAGAATT | 8440 |
rs62152200 | snp | G/T | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105794067 | TTTTTTTTTTTTTTG[G/T]AGACGGAATCTTGCT | 8440 |
rs62152201 | snp | C/T | 0.349671 | 0.229272 | intron-variant | NCK2 | GRCh38.p7 | 2:105795207 | TGGGTTCACTCTTTG[C/T]GTTGTGCATTCCATG | 8440 |
rs62152202 | snp | A/C | 0.111224 | 0.207945 | intron-variant | NCK2 | GRCh38.p7 | 2:105795612 | AGGGTGATTTCATTC[A/C]CCAAGGGATATTCAG | 8440 |
rs62152203 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | NCK2 | GRCh38.p7 | 2:105796741 | ATACCTCTATCAGAT[A/G]AATTAAATGAATTGG | 8440 |
rs62152204 | snp | G/T | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105812971 | CCACCCAGGGTGGCA[G/T]ATACCCCAGACAGAT | 8440 |
rs62152230 | snp | G/T | 0.441705 | 0.160466 | intron-variant | NCK2 | GRCh38.p7 | 2:105830717 | TGTGTGTGTGTGTGT[G/T]TGGTCTGATAATACC | 8440 |
rs62152231 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | NCK2 | GRCh38.p7 | 2:105837574 | CCCTGAGCACTGTGC[A/G]TGTCCCTGAGGCACA | 8440 |
rs62152232 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105838308 | TGGAATTTTATTAAA[A/T]TGTTTTTTTTTTTTT | 8440 |
rs62152233 | snp | C/G | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105839393 | TGGAGTGAAGTGCAT[C/G]GGAGAGAAGGGGTGG | 8440 |
rs62154114 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | NCK2 | GRCh38.p7 | 2:105755106 | ATGTGCTTCTGTTAT[A/T]GTCTTCTTAGGAGCT | 8440 |
rs62154115 | snp | A/G | 0.339203 | 0.233544 | intron-variant | NCK2 | GRCh38.p7 | 2:105755242 | TAGACAAGACCCAGC[A/G]GTAACTGTGAAGAAA | 8440 |
rs62154116 | snp | A/T | 0.343701 | 0.231776 | intron-variant | NCK2 | GRCh38.p7 | 2:105755489 | ATAAGAAGTAGGTTC[A/T]CCTTTCATGAGTGCC | 8440 |
rs62154117 | snp | A/G | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105758911 | TTAATGCTAGCATTC[A/G]AAACTAGTAAAATCA | 8440 |
rs62154118 | snp | A/C | 0.429087 | 0.174436 | intron-variant | NCK2 | GRCh38.p7 | 2:105764768 | CATCCTGAAAGAGAA[A/C]CTTTTCATATTTGCA | 8440 |
rs62154120 | snp | C/T | 0.345482 | 0.231048 | intron-variant | NCK2 | GRCh38.p7 | 2:105769025 | CACTCTCTAATCACA[C/T]GTTTTGTCTTTCTGG | 8440 |
rs62154121 | snp | A/G | 0.43978 | 0.162738 | intron-variant | NCK2 | GRCh38.p7 | 2:105769174 | TGTTGCTCAGTAAAT[A/G]CCAAGGGCTTTAGGA | 8440 |
rs62154124 | snp | C/T | 0.330016 | 0.236849 | intron-variant | NCK2 | GRCh38.p7 | 2:105771067 | AGCTGGGACTACAGG[C/T]GCCCGCCACCATGCC | 8440 |
rs62154125 | snp | C/T | 0.428182 | 0.17536 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771304 | TGGCGGGGTGGCTCA[C/T]GTGTGTAATCCCAGC | 8440 |
rs62154126 | snp | A/T | 0 | 0 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105773056 | AGCACCCCACTCAGC[A/T]AATTTTTTTTTTTTA | 8440 |
rs62155194 | snp | A/T | 0.330947 | 0.236533 | intron-variant | NCK2 | GRCh38.p7 | 2:105779588 | TGAAAAGGACTGCCC[A/T]TTCTTTGTGCTTTAC | 8440 |
rs66495264 | in-del | -/CT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105892498 | TTCAGAATCGTGGAC[-/CT]TACCTCCAGGTCTTT | 8440 |
rs66881299 | in-del | -/CTTAA | 0.373598 | 0.21731 | intron-variant | NCK2 | GRCh38.p7 | 2:105755406 | TTGAATTTGTTGCTT[-/CTTAA]CTTGATTGTGCCGAG | 8440 |
rs66939249 | multinucleotide-polymorphism | AC/GG | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105760625 | CTTTGTATCAACCAA[AC/GG]GTCTTTGCTTTCTGG | 8440 |
rs66953725 | in-del | -/ATT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105856333 | CTGACATTTAAAACG[-/ATT]TTGTTACCTTCTTAT | 8440 |
rs67022646 | in-del | -/A | | | intron-variant | NCK2 | GRCh38.p7 | 2:105782685 | TCGTTTCTGAGAGTG[-/A]GGGGATCCGGCCCGT | 8440 |
rs67123338 | in-del | -/ATATAT | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105844766 | TATATATATATATAT[-/ATATAT]GTATGTATGTATATA | 8440 |
rs67186970 | in-del | -/TGTGTGTGTGTGTGTG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105823133 | AAAGTCCTCTCATGC[-/TGTGTGTGTGTGTGTG]TGTGTGTGTGTGTGT | 8440 |
rs67259003 | in-del | -/TTAGA | | | intron-variant | NCK2 | GRCh38.p7 | 2:105770822 | GAAGTCATTTTGGGT[-/TTAGA]TAAACAGTTTGGCAT | 8440 |
rs67416364 | in-del | -/TTTTGC | 0.499793 | 0.0101816 | intron-variant | NCK2 | GRCh38.p7 | 2:105770920 | TGTTTGTTTGTTTGT[-/TTTTGC]TTTTGTTTTTGTTTT | 8440 |
rs67594123 | snp | C/G | 0.396727 | 0.202413 | intron-variant | NCK2 | GRCh38.p7 | 2:105809921 | GTTCCCAACACTGAG[C/G]GGGAGAGGGCAGGCA | 8440 |
rs67703944 | in-del | -/CA | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105780363 | ACACACACACACACA[-/CA]TTCATCTAAAGGACA | 8440 |
rs67864986 | in-del | -/A | 0.471388 | 0.116136 | intron-variant | NCK2 | GRCh38.p7 | 2:105832705 | TCAAAAAAAAAAAAA[-/A]TACTGGCAAAGTAAA | 8440 |
rs70953535 | in-del | -/C | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105800307 | ACACCTCATTACCCC[-/C]GTTCACAGCNNNNNN | 8440 |
rs70953537 | in-del | -/TATATATATATACACACATATATATATATATATA | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105835405 | ATATATATATATACG[lengthTooLong]TATATATATATATAT | 8440 |
rs70953538 | in-del | -/T | 0.104149 | 0.203046 | intron-variant | NCK2 | GRCh38.p7 | 2:105857047 | ATCTTGTAAATACAA[-/T]AAAAAAAAAAAAAAA | 8440 |
rs70953539 | in-del | -/A | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105858069 | TCCTATCTTTTTAGC[-/A]AAAAAAAAAAACAAA | 8440 |
rs70953540 | in-del | -/GT | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105864873 | CATTTGCAGGGAACC[-/GT]GTGTGTGTGTGTGTG | 8440 |
rs70953541 | in-del | -/TGTA/TGTG | 0 | 0 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105894019 | TATATATATATATAG[-/TGTA/TGTG]TGTGTGTGTGTGTGT | 8440 |
rs71250678 | in-del | -/A | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105858059 | TTAGCAAAAAAAAAA[-/A]CAAAAAAAAAACCCC | 8440 |
rs71379737 | multinucleotide-polymorphism | CA/TG | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105773926 | CAAGACAAAACCCTC[CA/TG]TTTATAAGAAAGATG | 8440 |
rs71379738 | in-del | -/G | 0.303938 | 0.244112 | intron-variant | NCK2 | GRCh38.p7 | 2:105863994 | TGGGGTCTCACTTGA[-/G]GGATGCAGAGTGCAA | 8440 |
rs71417368 | snp | A/G | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105766625 | ACTGTGCCTGGCCTA[A/G]GTTTTCTTTTTCTCC | 8440 |
rs71417369 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105781554 | ATCTGGTTTGCTGGC[A/G]TGAATCATGACCTGC | 8440 |
rs72034717 | in-del | -/AT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105844748 | TGGGGCGGGGGGGGA[-/AT]TATATATATATATAT | 8440 |
rs72078626 | in-del | -/TC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105774020 | GCTATCTTTTTTTTT[-/TC]TTTTTTGAGACGGAG | 8440 |
rs72101900 | in-del | -/ACACACAC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105780326 | GGGAGAGAGATATAT[-/ACACACAC]ACACACACACACACA | 8440 |
rs72315025 | in-del | -/CAAA/CACA/CACACA/CACACC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105750068 | ACACACACACACACA[-/CAAA/CACA/CACACA/CACACC]AAACAACAACAACAG | 8440 |
rs72339724 | in-del | -/AC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105780326 | GGGAGAGAGATATAT[-/AC]ACACACACACACACA | 8440 |
rs72342453 | in-del | -/TTG | 0.220843 | 0.248294 | intron-variant | NCK2 | GRCh38.p7 | 2:105884229 | GGACAAGTCCTTTGC[-/TTG]TTTTTTTCCCACCAT | 8440 |
rs72401438 | in-del | -/ATTT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105794723 | TTTATTTATTTATTT[-/ATTT]TTGAGACGGAGTCTT | 8440 |
rs72433026 | in-del | -/TT | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105765667 | GTGGGTTTTTTTTTT[-/TT]AATTACTAATATGTT | 8440 |
rs72497538 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105838311 | AATTTTATTAAAATG[-/T]TTTTTTTTTTTTGGC | 8440 |
rs72530041 | in-del | -/ATT/CAT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105856331 | AGCTGACATTTAAAA[-/ATT/CAT]CRTTGTTACCTTCTT | 8440 |
rs72823391 | snp | A/C | 0.223819 | 0.248625 | intron-variant | NCK2 | GRCh38.p7 | 2:105753076 | CAGCTAGACTCTGAC[A/C]AAGCTAGCCACCATC | 8440 |
rs72823396 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | NCK2 | GRCh38.p7 | 2:105759440 | TGTTGAAAGTCAACC[A/G]TGTTACCCTATGCAT | 8440 |
rs72823399 | snp | A/G | 0.0836354 | 0.186609 | intron-variant | NCK2 | GRCh38.p7 | 2:105761382 | GTCAGAATTAAGGCC[A/G]TTAGCCTGTTTCTCT | 8440 |
rs72825110 | snp | A/G | 0.429238 | 0.174281 | intron-variant | NCK2 | GRCh38.p7 | 2:105768605 | GGTTGTCCAACCCGC[A/G]GTCCAGGATGGCTTT | 8440 |
rs72825111 | snp | A/T | 0.440195 | 0.162252 | intron-variant | NCK2 | GRCh38.p7 | 2:105768678 | ATGAGTTTTTTTTGA[A/T]ATTTTCTTTTTCTCA | 8440 |
rs72825115 | snp | G/T | 0.419296 | 0.183954 | intron-variant | NCK2 | GRCh38.p7 | 2:105770927 | TTGTTTGTTTTTGCT[G/T]TTGTTTTTGTTTTGA | 8440 |
rs72825146 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105797489 | CTGCCAGGCTGTGCG[A/G]GCTAGCAGAAGGGAG | 8440 |
rs72825151 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105800607 | TAGTCTCAAAGTTCT[A/G]CTAAGGCCTAAGAAC | 8440 |
rs72825166 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105810255 | AAAAGTGTTAATAAT[A/G]GTTGTGTCTCACCTT | 8440 |
rs72825169 | snp | A/C | 0.0287284 | 0.116357 | intron-variant | NCK2 | GRCh38.p7 | 2:105814945 | AACGTTTATAATAGC[A/C]CCTGAAAATGACACA | 8440 |
rs72825182 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105824678 | TCACTGGGGCGTGCT[C/T]ATGTGTGGGTGTTGT | 8440 |
rs72825197 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | NCK2 | GRCh38.p7 | 2:105842818 | GGCAGGAGAGGGCGG[C/T]TGTGGTTTTGGAGGA | 8440 |
rs72825202 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105851901 | CTTCAGAAGCAGGTT[C/T]GGTTTTGTTTTGTTT | 8440 |
rs72827108 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105857047 | TTTTTTTTTTTTTTT[A/T]TTGTATTTACAAGAT | 8440 |
rs72827111 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | NCK2 | GRCh38.p7 | 2:105860848 | ATTAACCATTCCTTG[A/C]GACTGCAACTTGTGG | 8440 |
rs72935715 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105745657 | GAGAACTTAACCGTG[A/T]TTATTACAACTATTT | 8440 |
rs72935719 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NCK2 | GRCh38.p7 | 2:105756812 | TATCATTCTGAACTT[C/T]TTATTTTTTGAGACG | 8440 |
rs72935723 | snp | C/G | 0.0788843 | 0.182262 | intron-variant | NCK2 | GRCh38.p7 | 2:105761512 | CCATTATACACAGAT[C/G]AGAGAGACTCTGTTG | 8440 |
rs72935725 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105764270 | CAGCACCTTTGCATC[C/T]GCACCCTGCAGGTTA | 8440 |
rs72935748 | snp | C/T | 0.171057 | 0.237209 | intron-variant | NCK2 | GRCh38.p7 | 2:105777262 | GTTGCGGGGGGGCAA[C/T]GCTTTGCCCTTCCTC | 8440 |
rs72935761 | snp | C/G | 0.379354 | 0.213933 | intron-variant | NCK2 | GRCh38.p7 | 2:105786805 | CCTCCTGGGTTTGTT[C/G]CCCTCTGCCTCTCTT | 8440 |
rs72935784 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | NCK2 | GRCh38.p7 | 2:105816148 | AAACATTGGTTTCAA[A/G]ATACATAAAATTAGC | 8440 |
rs72935794 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | NCK2 | GRCh38.p7 | 2:105827382 | AACTACAAGGAGAAA[C/T]AGACATACCCATGAT | 8440 |
rs72937734 | snp | G/T | 0.0581099 | 0.160244 | intron-variant | NCK2 | GRCh38.p7 | 2:105863826 | TCTTAATCATTGAGT[G/T]ACTTTGAACAAGCCG | 8440 |
rs72937737 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | NCK2 | GRCh38.p7 | 2:105865371 | AAGAACACACAGTAC[A/G]TGCTGGGACTGACAT | 8440 |
rs72937739 | snp | A/C/G | 0.00993785 | 0.0698258 | intron-variant | NCK2 | GRCh38.p7 | 2:105869535 | GCACAAGTACGGTTC[A/C/G]GCTGTGTCTTTGCCA | 8440 |
rs72937747 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | NCK2 | GRCh38.p7 | 2:105889786 | AGATAGGGTCCCACT[A/C]TGTTGCCCAGGCTGA | 8440 |
rs73946287 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | NCK2 | GRCh38.p7 | 2:105749002 | TTGGCCTCTCTATTT[A/G]GCAAATTTTCTGTCA | 8440 |
rs73946288 | snp | A/T | 0.137527 | 0.223271 | intron-variant | NCK2 | GRCh38.p7 | 2:105749397 | CATGATGAGAGAATG[A/T]CATGTACTAATGCAT | 8440 |
rs73946293 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | NCK2 | GRCh38.p7 | 2:105776937 | TCCTAGGGGTTTCAT[A/G]TAGGCAGAATCTAGT | 8440 |
rs73946298 | snp | A/G | 0.021333 | 0.101051 | intron-variant | NCK2 | GRCh38.p7 | 2:105792566 | GTAAGGTCCACACAT[A/G]CAGCTGAATGATCTA | 8440 |
rs73946300 | snp | C/G | 0.021333 | 0.101051 | intron-variant | NCK2 | GRCh38.p7 | 2:105796568 | CGCAGGTGTTCAGAT[C/G]GGCAGCGTCTGGACT | 8440 |
rs73946301 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | NCK2 | GRCh38.p7 | 2:105796696 | GGCATCATGTTTATT[C/T]CCTTTCTTTTTTTTC | 8440 |
rs73946302 | snp | A/G | 0.0475351 | 0.146656 | intron-variant | NCK2 | GRCh38.p7 | 2:105797314 | TTTTCTGCACAGGAA[A/G]TAACCAATTTGTGCT | 8440 |
rs73946593 | snp | C/T | 0.021333 | 0.101051 | intron-variant | NCK2 | GRCh38.p7 | 2:105814932 | AACAACACAACTTAA[C/T]GTTTATAATAGCCCC | 8440 |
rs73946594 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | NCK2 | GRCh38.p7 | 2:105815236 | GTATTAAAATGATGC[A/G]GCCTTTAAAACAGTG | 8440 |
rs73946596 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | NCK2 | GRCh38.p7 | 2:105836563 | GGTAGTAGCAGGCCC[C/T]ATGCAGTCAGCTTTC | 8440 |
rs73946597 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | NCK2 | GRCh38.p7 | 2:105838714 | GCATCTTGTATCTGT[A/G]TGTCTACTGTGGTGA | 8440 |
rs73946603 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | NCK2 | GRCh38.p7 | 2:105863865 | TCTGAGCCTCAGTTG[C/T]GTCGTCTGTATAACG | 8440 |
rs73946604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105868738 | TCTTCAAAGCCTGCT[A/G]TACACAGTTACGTTT | 8440 |
rs73946605 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | NCK2 | GRCh38.p7 | 2:105874821 | TTTATTAGGACCCAA[A/T]CTTTAATGTCTGTAA | 8440 |
rs73946606 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | NCK2 | GRCh38.p7 | 2:105875782 | TTTATAAGTCAGTTG[A/G]TTTACAGTATTTTGT | 8440 |
rs73946607 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | NCK2 | GRCh38.p7 | 2:105875783 | TTATAAGTCAGTTGG[C/T]TTACAGTATTTTGTT | 8440 |
rs73946608 | snp | A/T | 0.5 | 0 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105894021 | CACACACACACACAC[A/T]ATATATATATATATT | 8440 |
rs73946609 | snp | A/C | 0.5 | 0 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105894022 | ACACACACACACACT[A/C]TATATATATATATTA | 8440 |
rs73949303 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | NCK2 | GRCh38.p7 | 2:105797617 | GGAGTCCCTGTGTGG[C/T]CTTTTGGAGATGAGT | 8440 |
rs73949304 | snp | A/G | 0.0475351 | 0.146656 | intron-variant | NCK2 | GRCh38.p7 | 2:105797749 | CAGTTAAAACAAAAC[A/G]CCTGATGTTGTGGCC | 8440 |
rs73949306 | snp | A/G | 0.0475351 | 0.146656 | intron-variant | NCK2 | GRCh38.p7 | 2:105799630 | TATTTTAAAGCAGAA[A/G]AACAAAACGGAATAC | 8440 |
rs73949307 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | NCK2 | GRCh38.p7 | 2:105799850 | ACTATGTTCTTGGCT[A/G]TGGAGACAGGATCAG | 8440 |
rs73949308 | snp | A/G | 0.0486741 | 0.148216 | intron-variant | NCK2 | GRCh38.p7 | 2:105800026 | TCATTTGGAAACACC[A/G]TCTTTGTTCATGTGG | 8440 |
rs73949309 | snp | C/T | 0.021333 | 0.101051 | intron-variant | NCK2 | GRCh38.p7 | 2:105801424 | TGCTTTTTTCTTTTT[C/T]TTTTTTTCTCCTCAC | 8440 |
rs73949310 | snp | A/G | 0.021333 | 0.101051 | intron-variant | NCK2 | GRCh38.p7 | 2:105801710 | GGGCTGGGTGTTTGG[A/G]GACAGAGTGGCCCTC | 8440 |
rs73949311 | snp | A/G | 0.021333 | 0.101051 | intron-variant | NCK2 | GRCh38.p7 | 2:105803401 | TCCTTAAGAAGGGCC[A/G]CTTCTGTGCTGTGCC | 8440 |
rs73949312 | snp | A/G | 0.021333 | 0.101051 | intron-variant | NCK2 | GRCh38.p7 | 2:105803482 | GAATACGTGTGACTG[A/G]TTTCATTCTACCAAC | 8440 |
rs73949313 | snp | C/T | 0.021333 | 0.101051 | intron-variant | NCK2 | GRCh38.p7 | 2:105803813 | GAAGCTTTTATAAAC[C/T]GCAGATGTTCTAATT | 8440 |
rs73949314 | snp | C/T | 0.021333 | 0.101051 | intron-variant | NCK2 | GRCh38.p7 | 2:105804754 | AAGAAATATGATATG[C/T]AAGAACCATTGTTTG | 8440 |
rs73950509 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | NCK2 | GRCh38.p7 | 2:105842512 | ATCTGAATCATATTA[C/T]ACATATGCTTTATGA | 8440 |
rs73950510 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | NCK2 | GRCh38.p7 | 2:105842760 | GGAGGCCTGACTGGG[G/T]TGGGGACAGTGAATG | 8440 |
rs73950511 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | NCK2 | GRCh38.p7 | 2:105844054 | TGGTCTTCCTCCCAA[A/G]AGCTAATACTGGAGC | 8440 |
rs73950512 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | NCK2 | GRCh38.p7 | 2:105846621 | TGTTCAGTTAAGAAA[C/T]TGATGTATACGTTAC | 8440 |
rs74265815 | in-del | -/TTT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105754693 | CTTTTTTTTTTTTTT[-/TTT]AAACTGCTCTGCATG | 8440 |
rs74265816 | in-del | -/AAA | | | intron-variant | NCK2 | GRCh38.p7 | 2:105843409 | AGAAAAAAAAAAAAA[-/AAA]CCTAGCCCTCCCCTC | 8440 |
rs74321962 | snp | A/C | 0.0554779 | 0.157039 | intron-variant | NCK2 | GRCh38.p7 | 2:105888661 | CTGCACTGAGCAACT[A/C]ACTTCTAATGACCAA | 8440 |
rs74379136 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | NCK2 | GRCh38.p7 | 2:105845604 | TTCAAATGTTGGCCA[A/G]GCTGGTCTCGAACTC | 8440 |
rs74389126 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | NCK2 | GRCh38.p7 | 2:105876760 | TAATGAAAGATGAGG[C/T]GATGAAGCGGAGATG | 8440 |
rs74389573 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | NCK2 | GRCh38.p7 | 2:105831019 | GCAAATACTTTCCCC[G/T]ATTCCAGAGTGTCTC | 8440 |
rs74399586 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | NCK2 | GRCh38.p7 | 2:105849630 | CTAAATGCTCTAATG[C/T]TCTTCAGGAAGTCAG | 8440 |
rs74424301 | snp | C/T | 0.0562307 | 0.157967 | intron-variant | NCK2 | GRCh38.p7 | 2:105782015 | CTGAAAACCTGCGGC[C/T]CATCAGGTCCCTCAA | 8440 |
rs74513754 | snp | C/T | 0.170733 | 0.237101 | intron-variant | NCK2 | GRCh38.p7 | 2:105836492 | GGGCTGGTTTTCAGG[C/T]CTCCAGGCTGCGTAT | 8440 |
rs74556944 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NCK2 | GRCh38.p7 | 2:105746748 | TGAAGAAGTGAACAC[A/G]AGGGAAAATCCTACC | 8440 |
rs74576377 | snp | G/T | 0.137527 | 0.223271 | intron-variant | NCK2 | GRCh38.p7 | 2:105748510 | CCACCTCAGGCAATC[G/T]TCCCACCTCAGCCTC | 8440 |
rs74593163 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105759474 | GGCTTTTATATAATA[A/T]AACATATGGTATATA | 8440 |
rs74662171 | snp | A/T | 0.0197687 | 0.0974348 | intron-variant | NCK2 | GRCh38.p7 | 2:105780249 | CTTCTCAGCATCTAG[A/T]TTAAGTTGGGACCTG | 8440 |
rs74737464 | snp | G/T | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105754289 | CCCAGCAATGGTGGG[G/T]GCAGCCAGGAAGTGA | 8440 |
rs74744092 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | NCK2 | GRCh38.p7 | 2:105821357 | CTGGAGGTCTCATGA[C/T]ACCTGGAAGTAACTT | 8440 |
rs74765169 | snp | G/T | 0.0521194 | 0.154759 | intron-variant | NCK2 | GRCh38.p7 | 2:105814811 | ACACAGGGCACACAG[G/T]GGGGAGGCCTGTATT | 8440 |
rs74790551 | snp | C/T | 0.0273246 | 0.113647 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893224 | CCCACGGTGGAGCTG[C/T]CCGCCCGGCCTTGTG | 8440 |
rs74815205 | snp | G/T | 0.02016 | 0.0983543 | intron-variant | NCK2 | GRCh38.p7 | 2:105847201 | GGGTACCTATTCCAG[G/T]TTTTCAAGATGAAAA | 8440 |
rs74815308 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | NCK2 | GRCh38.p7 | 2:105868247 | CTGTCCCTATGATCA[A/G]CTCCTCCAGGCTGAT | 8440 |
rs74887086 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | NCK2 | GRCh38.p7 | 2:105767081 | AGGCCCACACACACC[A/T]GTGCTGGGTTCCTGG | 8440 |
rs74934192 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | NCK2 | GRCh38.p7 | 2:105824681 | CTGGGGCGTGCTCAT[A/G]TGTGGGTGTTGTGCT | 8440 |
rs74959255 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | NCK2 | GRCh38.p7 | 2:105761741 | AAAAATGAGCTGGGT[A/G]TGGTGGCAAGTGCCT | 8440 |
rs74992515 | snp | G/T | 0.0166325 | 0.0896639 | intron-variant | NCK2 | GRCh38.p7 | 2:105854703 | CCTGAGAAAATGAGT[G/T]TCAACCTAACAGTTA | 8440 |
rs75007824 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | NCK2 | GRCh38.p7 | 2:105880117 | TTAGGGCTTTTCTAG[C/T]ATTTTTCCTCATGCA | 8440 |
rs75011107 | in-del | -/TTTTG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105770937 | TTGCTTTTGTTTTTG[-/TTTTG]AGACGGAGTCTCGCT | 8440 |
rs75042227 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105832859 | CTCTTTTTTTTTTTT[A/T]TTTTGTTTCGTTTCG | 8440 |
rs75221979 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105756345 | GTACAATCAATCTTT[C/T]CCTTTCTTCAGTCAT | 8440 |
rs75403993 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | NCK2 | GRCh38.p7 | 2:105800634 | GAACAAGAAACATTC[A/C]TCCTGTTTTTGGTCT | 8440 |
rs75415116 | snp | A/G | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105856333 | GCTGACATTTAAAAC[A/G]TTGTTACCTTCTTAT | 8440 |
rs75461089 | snp | A/G | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105860017 | GGGCTGGGCACGATG[A/G]TTTATGCCTGTAATC | 8440 |
rs75500612 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | NCK2 | GRCh38.p7 | 2:105814195 | CCATGTTAAACTTGG[A/G]CAGTCTTCATTTAAA | 8440 |
rs75759458 | snp | A/C | 0.0260105 | 0.111035 | intron-variant | NCK2 | GRCh38.p7 | 2:105768199 | ATTTGCTTTCTTTGC[A/C]TGTCTGTAGAGTCCA | 8440 |
rs75776375 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | NCK2 | GRCh38.p7 | 2:105881116 | GGATAAAATAGATCA[A/C]TTTAATTCTCAACTT | 8440 |
rs75793881 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | NCK2 | GRCh38.p7 | 2:105846349 | CATTTCAGAGAGTAA[A/G]TGAGTTGCTCAATGA | 8440 |
rs75837325 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | NCK2 | GRCh38.p7 | 2:105855561 | TCCTTGTATCAAAAC[A/G]TTAGAGGAGCCTGAC | 8440 |
rs76036943 | snp | A/T | 0 | 0 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105773059 | ACCCCACTCAGCAAA[A/T]TTTTTTTTTTTAATT | 8440 |
rs76051775 | snp | A/G | 0.159292 | 0.232964 | intron-variant | NCK2 | GRCh38.p7 | 2:105776231 | GACACCCCAACTTCC[A/G]TCCCAGCGACAGAAA | 8440 |
rs76098715 | snp | A/C | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105892184 | AGCAAAACTGCGTCT[A/C]AAAAAAAAAAAGAAT | 8440 |
rs76138225 | snp | A/C | 0.00636936 | 0.0560724 | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105743080 | GTGGGAAGACAACAA[A/C]CTCTCTAGAGGAGGC | 8440 |
rs76194661 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105878836 | GCTGCATGCTTGCTA[C/T]GTGCAATGTTCCAGT | 8440 |
rs76237091 | snp | C/T | 0.00597247 | 0.0543191 | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105743256 | GATAGAGAATGACAT[C/T]GGTGACTTCTAAAGA | 8440 |
rs76258987 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | NCK2 | GRCh38.p7 | 2:105784534 | GGAGCCTCGCTTGTG[A/G]AGGGTACAATGTAGA | 8440 |
rs76278282 | snp | G/T | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105876097 | ATACACAGCATGCCA[G/T]CCATTGGAAGGGTTT | 8440 |
rs76278833 | snp | G/T | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105842086 | TAGTATTTGTGGGGG[G/T]TTTTTTCTTTTTTTT | 8440 |
rs76437575 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NCK2 | GRCh38.p7 | 2:105804270 | TGTGTGTAAATGAAC[A/G]GACCAGCGCTTTTCT | 8440 |
rs76496845 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | NCK2 | GRCh38.p7 | 2:105825925 | GGAGTTCCTGGCTCC[A/G]TTAGATCTTGATGGA | 8440 |
rs76504160 | snp | A/G | 0.351853 | 0.228311 | upstream-variant-2KB, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105744677 | GCCCCGCGCTATCCC[A/G]GCGCCCGTACCGGGA | 8440 |
rs76551997 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | NCK2 | GRCh38.p7 | 2:105867016 | CTGTTAATCATCCTA[C/T]ATACCATTCAGACAT | 8440 |
rs76618514 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | NCK2 | GRCh38.p7 | 2:105760472 | AACCCCAGGTGTGCC[A/G]GCCAGGAGTCAGGCC | 8440 |
rs76647062 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | NCK2 | GRCh38.p7 | 2:105829761 | TCTCCCCCTTTCCCT[A/G]TGTACTCTTTGGAAG | 8440 |
rs76664537 | snp | G/T | 0.0260105 | 0.111035 | intron-variant | NCK2 | GRCh38.p7 | 2:105764183 | GTGCAATGATCCTTG[G/T]TGTGGGCCACAGCCT | 8440 |
rs76692119 | snp | A/G | 0.0562307 | 0.157967 | intron-variant | NCK2 | GRCh38.p7 | 2:105846680 | TAGACAATAACAGGC[A/G]TTGACAAGGATGTAG | 8440 |
rs76712631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105795338 | GCAATAGCATACTCT[A/G]TACACTTTTCCCAAG | 8440 |
rs76726445 | in-del | -/AAAAAAA | | | intron-variant | NCK2 | GRCh38.p7 | 2:105770136 | AAGTAAAAAAAAAAA[-/AAAAAAA]GAAAAAGGTATATTG | 8440 |
rs76751553 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105851265 | CGGCACAGAGCTGAG[C/T]TTTTTTTTTTTTTTC | 8440 |
rs76798017 | snp | C/T | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105829523 | AGTTGTCATGTCTCT[C/T]TGAGCTCTTCTTGGC | 8440 |
rs76807242 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | NCK2 | GRCh38.p7 | 2:105871430 | GTTTCCTCATGGGCT[A/G]TGTTGCCTGCAGTCT | 8440 |
rs76835062 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105785853 | TTCTCATTTGATGTG[C/T]TGAAGAAAATAAATA | 8440 |
rs76972003 | snp | A/G | 0.0825414 | 0.185628 | intron-variant | NCK2 | GRCh38.p7 | 2:105787215 | GAAGCTCAGCTCAGC[A/G]CCGTGGAAGGGGCAG | 8440 |
rs76973129 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NCK2 | GRCh38.p7 | 2:105816077 | GGGAAGAGGGAGTAC[A/G]TGTGTGTTGATGGAG | 8440 |
rs76977368 | snp | A/G | 0.100944 | 0.200705 | intron-variant | NCK2 | GRCh38.p7 | 2:105876190 | ACACCTCCAACCAAA[A/G]TGCTCAAAACCAGGT | 8440 |
rs77051085 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | NCK2 | GRCh38.p7 | 2:105858176 | TTTAGGCCAATTGTG[C/T]AGCCTGCAGAAATTA | 8440 |
rs77086632 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105866530 | GAAACTGTTCCACCT[C/T]AGATCATCAGCATTA | 8440 |
rs77145252 | snp | C/T | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105759446 | AAGTCAACCATGTTA[C/T]CCTATGCATACAGGC | 8440 |
rs77155991 | snp | A/G | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105770819 | CCAGGAAGTCATTTT[A/G]GGTTAAACAGTTTGG | 8440 |
rs77160880 | snp | A/C | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105875500 | AGATCGTGTTCCCCC[A/C]ATTCATATGTTGAAA | 8440 |
rs77177046 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105814068 | CTTTCAGGCTGATAC[C/T]GTTTTTTGCACAAAA | 8440 |
rs77181091 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NCK2 | GRCh38.p7 | 2:105746492 | GAAATTAACCTGGGC[C/T]GCTTTAACTTACCAA | 8440 |
rs77244969 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105823331 | TCATTCAAGTTGGGC[A/G]TGTCTGGTGGAGGGT | 8440 |
rs77309722 | snp | A/G | 0.172997 | 0.237846 | intron-variant | NCK2 | GRCh38.p7 | 2:105807423 | GTTCTTTGTAGAAAT[A/G]AAAAGTGCAAATTTT | 8440 |
rs77365178 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | NCK2 | GRCh38.p7 | 2:105751567 | ACATGCTGAGCTACA[A/G]GTCATCTGTGGCCAC | 8440 |
rs77365559 | snp | G/T | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105832717 | GTATTTTTTTTTTTT[G/T]TGAGGATTTTTGCAT | 8440 |
rs77374909 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | NCK2 | GRCh38.p7 | 2:105882537 | GCCACGGCAGGCAGC[C/G]CCACTGAGTTCATCT | 8440 |
rs77396012 | snp | G/T | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105838114 | GTCCTTTTTTTTTTT[G/T]TACCAGCAATAGATA | 8440 |
rs77428148 | snp | C/T | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105832847 | AAGAATTCTCTTCTC[C/T]TTTTTTTTTTTATTT | 8440 |
rs77519885 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105881168 | GAGGCAGCTGCCAGC[A/C]ACCGTATTTTTCTCA | 8440 |
rs77562819 | snp | A/C | 0.0333695 | 0.124785 | intron-variant | NCK2 | GRCh38.p7 | 2:105755954 | GGGAGAGAGACTAAA[A/C]ATATCACAAATTAGA | 8440 |
rs77574642 | snp | A/C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105759475 | GCTTTTATATAATAA[A/C/T]ACATATGGTATATAT | 8440 |
rs77614409 | snp | C/G | 1.72719e-05 | 0.00293865 | missense, utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893085 | AGCGGCGCTTCCACA[C/G]CATGGACGAGCTGGT | 8440 |
rs77623586 | snp | C/T | 0.0901694 | 0.192235 | intron-variant | NCK2 | GRCh38.p7 | 2:105877614 | AAAGAGAAAAGGTTT[C/T]TCTCTGCTTGGGCAT | 8440 |
rs77630970 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | NCK2 | GRCh38.p7 | 2:105808197 | GCCACTGTGCCTGGC[C/T]TCTTTCTTTGTTTCT | 8440 |
rs77654999 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | NCK2 | GRCh38.p7 | 2:105818688 | TTACAGTGGACATTT[A/G]TATAAAAAAACTTTA | 8440 |
rs77669559 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105872029 | TTTACTGCTTTTTCT[C/T]CATGGTGGTCAGGAA | 8440 |
rs77679813 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105851280 | CTTTTTTTTTTTTTT[C/T]TGAGACGGAGTCTCG | 8440 |
rs77734985 | snp | G/T | 0.166832 | 0.235761 | intron-variant | NCK2 | GRCh38.p7 | 2:105823086 | TAGGAAAAGCAGAGA[G/T]AAATTTTTCTTGACT | 8440 |
rs77779807 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | NCK2 | GRCh38.p7 | 2:105872058 | AATTTAGAATTTCTT[C/T]TTCCTTAAACGTACG | 8440 |
rs77820705 | snp | A/T | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105871658 | CCACCACACCCAGCT[A/T]ATTTTTTTGTATTTT | 8440 |
rs77830381 | snp | A/G | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105782685 | ATCGTTTCTGAGAGT[A/G]GGGGATCCGGCCCGT | 8440 |
rs77854346 | snp | A/T | 0.0217236 | 0.101931 | intron-variant | NCK2 | GRCh38.p7 | 2:105803990 | CATGGATTGCAAGAC[A/T]GAGGAGTAAATTAAC | 8440 |
rs77936916 | snp | C/G | 0.0240643 | 0.107019 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893230 | GTGGAGCTGCCCGCC[C/G]GGCCTTGTGGCAGAG | 8440 |
rs77949950 | snp | C/T | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105793674 | GTGTGTATTTTTACC[C/T]ACTGCAGTTGACACC | 8440 |
rs77956611 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105751909 | AGATGTAATCATAAT[G/T]TTCTGGTAGCCACAT | 8440 |
rs78052211 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | NCK2 | GRCh38.p7 | 2:105803323 | GTTTTCTTGCAGCAG[A/G]TATCATAAATAGGCA | 8440 |
rs78084205 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105848092 | TTCAAGCCATTGAGC[C/G]TAGTGATGACTGGGC | 8440 |
rs78126121 | snp | A/C | 0.0479149 | 0.147179 | downstream-variant-500B | NCK2 | GRCh38.p7 | 2:105894563 | CAGCGCTCTCACACC[A/C]TGTGTCCCCCACGAC | 8440 |
rs78141353 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | NCK2 | GRCh38.p7 | 2:105799680 | AAAAGCTAATTACCA[C/T]GTTTACATAAATGGT | 8440 |
rs78176059 | snp | C/T | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105838103 | TAACTAGAACAGTCC[C/T]TTTTTTTTTTGTACC | 8440 |
rs78229412 | snp | C/T | 0.161924 | 0.233971 | intron-variant | NCK2 | GRCh38.p7 | 2:105844299 | GACAAGAAAAGGACA[C/T]TAAGGGAAAGCTAAG | 8440 |
rs78336162 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105884373 | CTGACATAATTCCTT[A/C]GCAGCATGCCAGGAT | 8440 |
rs78422411 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105867883 | AAGAAACGTGAACCA[A/C]ATATGCCAGGGAATT | 8440 |
rs78484903 | snp | G/T | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105849955 | ATGAGGTATTACCCT[G/T]GGCTATTGAAGAGGC | 8440 |
rs78527978 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105808036 | GCCTCTTGAGTAGCC[A/G]GGACTACAGGTGTGT | 8440 |
rs78537698 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | NCK2 | GRCh38.p7 | 2:105753121 | TATCTGAAAATACAT[A/C]AAACAGAACTGTAAA | 8440 |
rs78556826 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105846859 | ATGGGTGTACAAATA[C/T]CTCTTCAAGACTCTG | 8440 |
rs78570378 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | NCK2 | GRCh38.p7 | 2:105875486 | GGCCAAGCTGCCTCA[C/G]ATCGTGTTCCCCCCA | 8440 |
rs78573062 | snp | A/G | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105770821 | AGGAAGTCATTTTGG[A/G]TTAAACAGTTTGGCA | 8440 |
rs78573928 | snp | A/G | 0.031825 | 0.122064 | intron-variant | NCK2 | GRCh38.p7 | 2:105842727 | AGTACTCACAGCAAA[A/G]ACTGCAGGTGGGCTC | 8440 |
rs78576706 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105886276 | CTGCAAGATCATGCA[A/G]TACAGGCTGTTATCT | 8440 |
rs78576957 | snp | C/T | 0.164219 | 0.234823 | intron-variant | NCK2 | GRCh38.p7 | 2:105839158 | AAGAGCATTCCAATG[C/T]GAAGACCCCAAGGTG | 8440 |
rs78578698 | snp | A/C | 0.0209421 | 0.100162 | intron-variant | NCK2 | GRCh38.p7 | 2:105878344 | CTGTGTTTGGAGACA[A/C]AGCCTTTACAGGGGT | 8440 |
rs78592565 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105865765 | CGCTGCCGCATGAGT[C/T]ATCTTCAGCATCTTT | 8440 |
rs78621533 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105863839 | GTGACTTTGAACAAG[C/T]CGCTGAAGCTTCTGA | 8440 |
rs78689306 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105817287 | TTACAATAAAATCAT[A/G]ACTGTGATGCAACAT | 8440 |
rs78718400 | snp | A/T | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105871660 | ACCACACCCAGCTAA[A/T]TTTTTTGTATTTTTA | 8440 |
rs78719685 | snp | C/G | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105777251 | CGAGCCGGGGTGTTG[C/G]GGGGGGGCAACGCTT | 8440 |
rs78796871 | snp | G/T | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105838113 | AGTCCTTTTTTTTTT[G/T]GTACCAGCAATAGAT | 8440 |
rs78802775 | snp | G/T | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105794065 | TTTTTTTTTTTTTTT[G/T]GGAGACGGAATCTTG | 8440 |
rs78887212 | snp | A/T | 0.277778 | 0.248452 | intron-variant | NCK2 | GRCh38.p7 | 2:105889589 | TTTTTTTTTTTTTTT[A/T]TTTAATTATTTTGAG | 8440 |
rs78949550 | snp | A/T | 0.0532157 | 0.154195 | intron-variant | NCK2 | GRCh38.p7 | 2:105829135 | TGCTTTCTTTTTAAA[A/T]TTTCCATTTGTGATA | 8440 |
rs78978175 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | NCK2 | GRCh38.p7 | 2:105755706 | TTGAGACCCGAACCC[A/C]TGCCTATAAATTCGT | 8440 |
rs79003301 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | NCK2 | GRCh38.p7 | 2:105882469 | GGTTTCTGACACCTC[C/T]TTTTGTTGTTTGCTT | 8440 |
rs79057216 | snp | A/G | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105846479 | GTAGATACTCACTGA[A/G]AAAAAAAAAATAATA | 8440 |
rs79087661 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | NCK2 | GRCh38.p7 | 2:105780325 | TGGGAGAGAGATATA[C/T]ACACACACACACACA | 8440 |
rs79091742 | snp | C/T | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105756347 | ACAATCAATCTTTCC[C/T]TTTCTTCAGTCATCC | 8440 |
rs79095165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105811709 | CATGATGCTTGCAGG[C/T]GGGTGCGGGTCTCCT | 8440 |
rs79134111 | snp | A/G | 0.198634 | 0.244666 | intron-variant | NCK2 | GRCh38.p7 | 2:105839979 | TCTGCTGTAGTGGAC[A/G]TGCAGGTAACAAGAG | 8440 |
rs79187408 | snp | C/T | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105832846 | GAAGAATTCTCTTCT[C/T]TTTTTTTTTTTTATT | 8440 |
rs79267844 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | NCK2 | GRCh38.p7 | 2:105813393 | GACAGCACCCAGTGG[C/T]ATTATGTCCACAAAG | 8440 |
rs79303774 | snp | A/G | 0.00597247 | 0.0543191 | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105743244 | CCACTGGATTTAGAT[A/G]GAGAATGACATCGGT | 8440 |
rs79312036 | snp | C/T | 0.00597247 | 0.0543191 | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105744276 | ATGATGGACTAAAAA[C/T]GTGTCTGGTTGGGAA | 8440 |
rs79315827 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | NCK2 | GRCh38.p7 | 2:105844267 | AATGTAGTGTGGGAT[C/G]CTGGGTGGGATCTTG | 8440 |
rs79320642 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105804294 | CTTTTCTTTGATGTT[C/T]GCACTGGATGAGGAT | 8440 |
rs79322481 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | NCK2 | GRCh38.p7 | 2:105863311 | TGAAATGAAATGTGG[G/T]TAACAAATGCAGCAG | 8440 |
rs79342548 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105777252 | GAGCCGGGGTGTTGC[C/G]GGGGGGCAACGCTTT | 8440 |
rs79523958 | snp | A/T | 0.0418186 | 0.138422 | intron-variant | NCK2 | GRCh38.p7 | 2:105804693 | GCTTGCAAATTTATT[A/T]ATTGAATGAAATACT | 8440 |
rs79551650 | snp | A/T | 0.0174175 | 0.0916809 | intron-variant | NCK2 | GRCh38.p7 | 2:105856551 | ACCAAATGTGGTGGG[A/T]GTTGCAAAATGTTCA | 8440 |
rs79557117 | snp | G/T | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105770922 | TTTGTTTGTTTGTTT[G/T]TGCTTTTGTTTTTGT | 8440 |
rs79689040 | snp | G/T | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105818210 | GCATGTTCTAACTCA[G/T]AGGTGGGAATTGAAC | 8440 |
rs79732631 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NCK2 | GRCh38.p7 | 2:105776687 | CAGCCAGCCTCCCTC[A/G]TTTTAGCTCAGCCAT | 8440 |
rs79744235 | snp | C/T | 0.164873 | 0.23506 | intron-variant | NCK2 | GRCh38.p7 | 2:105827160 | GCCTACCACCACGCC[C/T]GGCTAATTTTTGGTA | 8440 |
rs79747582 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105838162 | TTAGCATTTTCAAGT[A/C]ACAAGAAAATCTTGT | 8440 |
rs79749836 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | NCK2 | GRCh38.p7 | 2:105864483 | AAGTAAGAGGAGACT[A/G]AGCCACGGTGCGTAG | 8440 |
rs79778497 | snp | A/T | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105779694 | GGAAAGAGCTTTGAT[A/T]TTTTTTTTTCCCACT | 8440 |
rs79778620 | snp | G/T | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105873672 | TTTTATTTTTTGGGG[G/T]CTCTTAATTGAAGAG | 8440 |
rs79799777 | in-del | -/GGGAGGG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105818300 | GGGGAGGGGGGAGGG[-/GGGAGGG]ATAGCATTAGGAGAT | 8440 |
rs79837167 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105759547 | CAGAAAAAGTTTCAA[A/G]GATAATACAGAGAAT | 8440 |
rs79841282 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105747620 | GAGTGATGTTTGGAA[A/G]AACAAGTAAGCTAAC | 8440 |
rs79869949 | snp | C/T | 0.00597247 | 0.0543191 | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105743542 | GAGCTTGTACCTGAT[C/T]CCTGCTCAGTGTACT | 8440 |
rs79941679 | snp | A/C | 0.0228947 | 0.104514 | intron-variant | NCK2 | GRCh38.p7 | 2:105836343 | TTGATTCTGGGTGAG[A/C]GTAAAAGTGTAGTCT | 8440 |
rs79965424 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | NCK2 | GRCh38.p7 | 2:105832192 | TGTTATTGGTATATA[G/T]AAGAAACACTACTGA | 8440 |
rs79973949 | in-del | -/TT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105801430 | TTTCTTTTTTTTTTT[-/TT]CTCCTCACAGTCTAT | 8440 |
rs80007076 | snp | A/T | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105853008 | ATAAAAAAATTTTTT[A/T]AGCATCTAGTAGAAA | 8440 |
rs80039360 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | NCK2 | GRCh38.p7 | 2:105888194 | GGAAAATGACTTCTG[A/T]AAAGAAGGGTCAAAT | 8440 |
rs80121605 | in-del | -/AA | 0.179519 | 0.239859 | intron-variant | NCK2 | GRCh38.p7 | 2:105846478 | GGTAGATACTCACTG[-/AA]AAAAAAAAAATAATA | 8440 |
rs80232088 | snp | C/T | 0.0115144 | 0.0749975 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893687 | TGGAACCACCGGGTG[C/T]GATGGCAGTGAGGAG | 8440 |
rs80250970 | snp | C/T | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105806236 | CATATCACATTTTCT[C/T]TCTTTTTTTTTTTTT | 8440 |
rs80253156 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105843729 | AGCCGTAAGATCACA[A/G]TGATATAAATGATGG | 8440 |
rs80269510 | snp | A/C | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105837560 | CATAAGCAGTACTGC[A/C]CTGAGCACTGTGCAT | 8440 |
rs80284711 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105796610 | CTGGAAGGCTGGAGA[C/T]GGTGCTTTTCTTCCT | 8440 |
rs80286292 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | NCK2 | GRCh38.p7 | 2:105873995 | ATGGCCAGCAAAGGC[A/G]GGGGAAGGCTCGGGG | 8440 |
rs80325475 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | NCK2 | GRCh38.p7 | 2:105838150 | TATTTATAAACCTTA[A/G]CATTTTCAAGTCACA | 8440 |
rs80346085 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | NCK2 | GRCh38.p7 | 2:105840234 | TCCAGGGAATAATTA[C/T]AGGAGCAGGTTCCTT | 8440 |
rs111320888 | in-del | -/A | 0.40595 | 0.195396 | intron-variant | NCK2 | GRCh38.p7 | 2:105892845 | GTGAAACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 8440 |
rs111415279 | snp | C/T | 0.195526 | 0.243993 | intron-variant | NCK2 | GRCh38.p7 | 2:105754679 | AGCTCCCCCAACAAC[C/T]TTTTTTTTTTTTTTT | 8440 |
rs111478368 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | NCK2 | GRCh38.p7 | 2:105808469 | AATCACGGATTAATC[A/G]GGTGGTTCTCAGTGC | 8440 |
rs111519689 | snp | A/G | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105830761 | TGATACCTTATTGTG[A/G]CTTTGATTTGCATTT | 8440 |
rs111546674 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105795358 | CTTTTCCCAAGCAAG[A/C]GGTCAAAGGTGGTTT | 8440 |
rs111592011 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NCK2 | GRCh38.p7 | 2:105776358 | GAAGCAGCCAAAGCA[C/T]GTTTGGGGGAGGGAG | 8440 |
rs111650956 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105794860 | ATTATCTAAACTGTT[C/G]GCATGGTTCCGCAGC | 8440 |
rs111651210 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | NCK2 | GRCh38.p7 | 2:105836187 | TTTCCTTGCTTTTTC[G/T]TGTTTCTTGTATCTG | 8440 |
rs111652229 | in-del | -/T/TT | 0.491885 | 0.0631791 | intron-variant | NCK2 | GRCh38.p7 | 2:105831410 | AATAAGCATGATATC[-/T/TT]TTTTTTTTTTTTTTG | 8440 |
rs111653462 | snp | G/T | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105836127 | GATTTCCTTTTCTTT[G/T]TTCTGTTATTAGAGA | 8440 |
rs111654397 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105889543 | TCTGCTACAGCAGGG[C/T]TGAGGCAGAGCCTGA | 8440 |
rs111659615 | snp | A/G | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105821200 | CTACTCACTTTTATC[A/G]TATCCTGGTTGTTTG | 8440 |
rs111829870 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105762668 | GCCCATAGCATTTAC[A/G]GTCATCAGAGAAATG | 8440 |
rs111870003 | snp | C/T | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105795389 | TCTAATTATATGGTA[C/T]ATTGTAACTTAATCA | 8440 |
rs111907997 | snp | A/G | 0.031825 | 0.122064 | intron-variant | NCK2 | GRCh38.p7 | 2:105855543 | GACCCCTGCACAGGT[A/G]TCTCCTTGTATCAAA | 8440 |
rs111959325 | snp | G/T | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105795441 | GGGCCTGTTTATTTA[G/T]TTATTTTGAAACGGG | 8440 |
rs111964256 | snp | C/T | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105759479 | TTATATAATAAAACA[C/T]ATGGTATATATTTTT | 8440 |
rs111982296 | snp | G/T | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105804278 | AATGAACGGACCAGC[G/T]CTTTTCTTTGATGTT | 8440 |
rs112166148 | snp | G/T | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105892121 | CCTGGGAGGCGCAGG[G/T]TGCAGTGAGCCAAGA | 8440 |
rs112190567 | snp | A/G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105883392 | AATATTAAGTGCTTG[A/G/T]TCCAGAGTCCTTAAG | 8440 |
rs112262780 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | NCK2 | GRCh38.p7 | 2:105835368 | TTGGCTGGTTTTATA[A/T]ATATATACATATATA | 8440 |
rs112423115 | snp | A/G | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105805448 | ATTTCTATTTAATTG[A/G]AATAATAATAAATTT | 8440 |
rs112443806 | snp | A/G | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105844792 | TGTATATATGTATAT[A/G]AAAGAATATATAAAT | 8440 |
rs112443960 | snp | G/T | | | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105744920 | GATCGTCAGGCCGGA[G/T]CCGCGCGGCCGAGCG | 8440 |
rs112446391 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105794122 | GGCGCCATTTTGGCT[C/T]ACTGCAACCTCCACC | 8440 |
rs112497297 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NCK2 | GRCh38.p7 | 2:105766476 | CTACAGGCATACACC[A/G]GCCCCAGTGAAGTTT | 8440 |
rs112606988 | in-del | -/G | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105890171 | TGCTCAGGAGCCCAC[-/G]AAATTAAAAATTACC | 8440 |
rs112627277 | snp | C/T | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105879726 | CAGCAGCCCAGCTCT[C/T]CACCATTGAGGACAA | 8440 |
rs112634966 | snp | A/G | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105870210 | CGGGGCCAAGCAGGG[A/G]CCCTACAGGTGCTCC | 8440 |
rs112878758 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105795208 | GGGTTCACTCTTTGC[A/G]TTGTGCATTCCATGG | 8440 |
rs112885404 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771396 | ACATAGTGAATCCCC[A/G]TTTCTATTAAAAATA | 8440 |
rs112962756 | snp | C/T | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105842109 | TTTTTTTTTTTGAGC[C/T]GGAGTTTCTCTCGTT | 8440 |
rs112986524 | snp | G/T | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105858058 | TGGGGTTTTTTTTTT[G/T]TTTTTTTTTTTGCTA | 8440 |
rs113000163 | snp | A/G | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105836044 | TTCGTTGAATTTTCC[A/G]TGTTCCCATGTATCT | 8440 |
rs113016586 | snp | A/C | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105870067 | TCCTTTGCCCCAACA[A/C]CTCCCTTTCAGAGCT | 8440 |
rs113059254 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | NCK2 | GRCh38.p7 | 2:105856728 | CATACCAGCTCACTG[A/G]CCATCGTAGATTCTC | 8440 |
rs113066308 | snp | A/C/G | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105785825 | GTAAGTGCTGAGTCT[A/C/G]TTTATTTAGCTGTTC | 8440 |
rs113075664 | snp | A/G | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105770820 | CAGGAAGTCATTTTG[A/G]GTTAAACAGTTTGGC | 8440 |
rs113171718 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | NCK2 | GRCh38.p7 | 2:105799466 | AGGCTGTCTCTTCCC[A/T]GGGGACTTGACTTGA | 8440 |
rs113202353 | snp | C/T | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105783299 | TGGGTGGGCCCCCAT[C/T]GCCCTCCTCCTTTGG | 8440 |
rs113224718 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | NCK2 | GRCh38.p7 | 2:105816754 | AAGCTTTCAATGAGG[A/G]AGAAAATTAGATTAT | 8440 |
rs113334925 | in-del | -/AA/AAA | 0.288386 | 0.247035 | intron-variant | NCK2 | GRCh38.p7 | 2:105817175 | GCAAGACTTGGTCTC[-/AA/AAA]AAAAAAAAAAAAAAA | 8440 |
rs113351363 | snp | A/G | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105815950 | TCAGGTCCCTTGATT[A/G]TGGGCTGGCTGTTCC | 8440 |
rs113354388 | snp | A/G | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105830693 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 8440 |
rs113420409 | snp | A/C | 0.00179384 | 0.0298948 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881473 | GTTCGCCTATGTGGC[A/C]GAGCGGGAGGATGAG | 8440 |
rs113468666 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | NCK2 | GRCh38.p7 | 2:105792002 | TGGGTTAGCGGTTGA[G/T]TCTGAAAAGCAAGCT | 8440 |
rs113559177 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | NCK2 | GRCh38.p7 | 2:105812636 | AGGCCTATGCTAATC[C/T]ATGCTTTTTTGTTTT | 8440 |
rs113626806 | snp | A/C | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105871139 | CGAGTGAGGTTTATT[A/C]ATTGCAGATGTGTAT | 8440 |
rs113651650 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | NCK2 | GRCh38.p7 | 2:105799411 | GCTCCAGCTTTCTTT[C/T]AGATGGCCAACCAGA | 8440 |
rs113711451 | snp | G/T | 0.0174175 | 0.0916809 | intron-variant | NCK2 | GRCh38.p7 | 2:105807251 | GGAAGGGCCGCCCTC[G/T]CAGACATCATGTTCT | 8440 |
rs113713763 | snp | A/C/G | 1.74102e-05 | 0.00295039 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893205 | CCACACTCGCCTCCC[A/C/G]GGCCCCACGGTGGAG | 8440 |
rs113719857 | snp | C/G | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105876791 | TGTAGAAAAACTACA[C/G]AGAGAGAATGAAAGG | 8440 |
rs113720264 | in-del | -/TTAGA | 0.300169 | 0.244914 | intron-variant | NCK2 | GRCh38.p7 | 2:105770821 | GGAAGTCATTTTGGG[-/TTAGA]TTAAACAGTTTGGCA | 8440 |
rs113805713 | snp | C/T | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105814900 | TCTGGGCAAATTCAC[C/T]TCCCAGTTAAAATCT | 8440 |
rs114018770 | snp | C/G | 0.0387552 | 0.1337 | intron-variant | NCK2 | GRCh38.p7 | 2:105870869 | ACAGCCAGTAACAGC[C/G]GTGCTTTCACCCTAG | 8440 |
rs114024171 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | NCK2 | GRCh38.p7 | 2:105785306 | GGAGCCGAGGTGGCC[A/G]TGCTGTGTGTGTCCA | 8440 |
rs114027546 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | NCK2 | GRCh38.p7 | 2:105747680 | ACAGCTCACTTCAGA[G/T]GCTTAGGAAATTAGT | 8440 |
rs114031547 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | NCK2 | GRCh38.p7 | 2:105750377 | TGAAGCGTCCTGTCT[C/G]CAAATATAGTCACTT | 8440 |
rs114034521 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105813887 | AATTGCCTTCCAGCC[C/G]TCCCTCCTTTATTTC | 8440 |
rs114041584 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105769106 | GGTCACCTCATTAGC[A/G]TAAGCTCAGGTGTGG | 8440 |
rs114046263 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | NCK2 | GRCh38.p7 | 2:105828413 | ATGTTGGTCAAATTT[A/G]AAAAATGGCACTGAC | 8440 |
rs114050254 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | NCK2 | GRCh38.p7 | 2:105867944 | TGCATTTACCCATAC[A/G]GTGTGCTTTCTTTTT | 8440 |
rs114071060 | snp | A/G | 0.0263992 | 0.111815 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771490 | AGAATCACTTGACCC[A/G]AGAGGTGAATGTTGC | 8440 |
rs114079823 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | NCK2 | GRCh38.p7 | 2:105768886 | GACACCTCCTAGTGC[A/G]CCATCCCAATGAGTT | 8440 |
rs114084782 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105817175 | GGCAAGACTTGGTCT[A/C]AAAAAAAAAAAAAAA | 8440 |
rs114098359 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | NCK2 | GRCh38.p7 | 2:105839280 | CTGGGGTTTGCAGAG[A/G]GGACTGACACAAATA | 8440 |
rs114107857 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | NCK2 | GRCh38.p7 | 2:105862211 | GAATTATGTCTAGGA[A/G]GAATTAGAGGGCTTC | 8440 |
rs114115044 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | NCK2 | GRCh38.p7 | 2:105794870 | CTGTTCGCATGGTTC[C/T]GCAGCCAAAGATGGT | 8440 |
rs114125327 | snp | G/T | 0.030278 | 0.119257 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105772334 | AATAAACAGCACTAA[G/T]CATCCTTCCCATTTG | 8440 |
rs114128601 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | NCK2 | GRCh38.p7 | 2:105777423 | GACTCCTGAGAGTGT[A/G]GGTGGAATGAAATGA | 8440 |
rs114171298 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | NCK2 | GRCh38.p7 | 2:105829132 | GTATGCTTTCTTTTT[A/G]AAATTTCCATTTGTG | 8440 |
rs114173496 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105878419 | TAACTGGTGTTCTTA[C/T]AAGAAAAGGAGATTG | 8440 |
rs114180891 | snp | G/T | 0.0314385 | 0.121371 | intron-variant | NCK2 | GRCh38.p7 | 2:105848484 | AAAATAACATACTGA[G/T]CAAAGGTCTTACTGA | 8440 |
rs114192747 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | NCK2 | GRCh38.p7 | 2:105784354 | CTGCTGATCGGACTC[A/C]TTGTGGTGGTCATAT | 8440 |
rs114201206 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105879704 | GGTAGTGGCAGTGGG[A/G]GGGGGGCAGCAGCCC | 8440 |
rs114211250 | snp | A/T | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105850112 | TTTTACAGAAGAAAC[A/T]GAAATCCAAGGAGAA | 8440 |
rs114242192 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | NCK2 | GRCh38.p7 | 2:105816363 | AATAAATAACCAGTT[A/G]TTTTTAAAAGTGGTT | 8440 |
rs114246299 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NCK2 | GRCh38.p7 | 2:105860590 | GCCTTACTGGGCTGT[A/G]CACAGGACTCAAGCA | 8440 |
rs114247150 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | NCK2 | GRCh38.p7 | 2:105762705 | ATTTTCCTGTTACAT[A/G]ATAGTGATGCACGTG | 8440 |
rs114305959 | snp | A/T | 0.0263992 | 0.111815 | intron-variant | NCK2 | GRCh38.p7 | 2:105795036 | TTTTAGAGCAGTTTT[A/T]GTTTCACAGCAAAAC | 8440 |
rs114313073 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105808948 | GCTGGGGTGTGACTG[C/T]ATGTACAATTGTTGA | 8440 |
rs114320557 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | NCK2 | GRCh38.p7 | 2:105787008 | CCTTGGTGGCTCTCA[A/G]TGGGGTGAGCATGTG | 8440 |
rs114335974 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | NCK2 | GRCh38.p7 | 2:105879893 | TTGGAGGAAGTCATT[C/T]TGAGGAGTCTACAAA | 8440 |
rs114341196 | snp | A/G/T | 0.0225289 | 0.10389 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105772730 | TTTTCCCCGAAACTC[A/G/T]TCTTTCTGGAATTGA | 8440 |
rs114347220 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NCK2 | GRCh38.p7 | 2:105811547 | CAGCCTGGAGATTCA[A/G]TCCTTGTCTTTAAGG | 8440 |
rs114375167 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | NCK2 | GRCh38.p7 | 2:105873064 | CTTCCATATCCCACA[A/C]CCCCAGTTCCATGAT | 8440 |
rs114410741 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | NCK2 | GRCh38.p7 | 2:105797035 | GAAATGGATTTAGTC[A/G]TCACAGTCCCTTTTT | 8440 |
rs114426572 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NCK2 | GRCh38.p7 | 2:105845591 | GTAGAGGTGAGGTTT[C/T]AAATGTTGGCCAGGC | 8440 |
rs114445626 | snp | C/T | 0.031825 | 0.122064 | intron-variant | NCK2 | GRCh38.p7 | 2:105842841 | TTGGAGGAATGAGTT[C/T]TCAGGGGGGTGGACG | 8440 |
rs114453281 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | NCK2 | GRCh38.p7 | 2:105791350 | TGCCTTCACGTTTTT[C/T]TCTTCACTCCAGAAG | 8440 |
rs114455235 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | NCK2 | GRCh38.p7 | 2:105815716 | GCTTTTTAGCCCAAG[A/G]CTATGGGTCCGGTTG | 8440 |
rs114466993 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | NCK2 | GRCh38.p7 | 2:105769657 | CATGGGGTAATTAGA[A/G]TCATTGGCCAAGAAG | 8440 |
rs114509843 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | NCK2 | GRCh38.p7 | 2:105889654 | AGTGGCCCTGTCATA[C/T]CTCACTGTTGCCTTG | 8440 |