SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs868227 | snp | A/G | 0.216649 | 0.247765 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125251228 | CCATACCCATTAGAA[A/G]GTTTCAGGGAGACGC | 286053 |
rs954889 | snp | A/G | 0.163564 | 0.234582 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125131544 | CTGGGCAAGGTGTGC[A/G]TAAGTTCCAATATCT | 286053 |
rs955840 | snp | C/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125209953 | TTTATTTGCATAGGA[C/T]TTTGCAGTTTACAAA | 286053 |
rs1106264 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125181503 | CTTCAACCTTTCTGC[A/G]TATTTGAAAATTTAT | 286053 |
rs1109964 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125251607 | CTTCTGCCCAGGAAT[A/G]TATGCTGGAAACTTG | 286053 |
rs2293890 | snp | C/G | 0.478932 | 0.10045 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125357656 | ATCAACTTCCAGTAG[C/G]TGTTTCGTCCTAGTC | 286053 |
rs2384859 | snp | A/T | 0.494526 | 0.0520291 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125189884 | CACAGAATATGGCTT[A/T]AGTCACTTAAGTGTG | 286053 |
rs2384860 | snp | G/T | | | intron-variant, downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125196013 | tgcctcccaagtagc[G/T]gggattacagggccc | 286053 |
rs2384862 | snp | C/T | | | intron-variant, downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125196029 | gggattacagggccc[C/T]gccaccatgtgaaag | 286053 |
rs2384864 | snp | A/C | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125210338 | CTGATATATGCTAAT[A/C]ATGTTTTTCTCTGGG | 286053 |
rs2384865 | snp | G/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125210352 | TAATGTTTTTCTCTG[G/T]GGAATTCTTCCTTTA | 286053 |
rs2384866 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125210399 | TTTTCCTGAAAGAGA[A/G]AGGCTCATTTGAGGG | 286053 |
rs2384868 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125210444 | CAATTTTTAATGTCC[C/T]CAGCAGCTTATAATA | 286053 |
rs2384869 | snp | A/G | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125210456 | TCCCCAGCAGCTTAT[A/G]ATAGACATTCAATAA | 286053 |
rs2384870 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217405 | ttgctgtgtcaccca[A/G]gctgaagtgcagtgg | 286053 |
rs2384871 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217461 | tgcctcccaggttca[A/T]gccattctcctgtct | 286053 |
rs2384872 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217509 | ggactacggggcacc[C/T]accagccacacatgg | 286053 |
rs2384873 | snp | A/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217528 | gccacacatggctaa[A/T]tttggttttttggaa | 286053 |
rs2384874 | snp | A/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218040 | TAATTTGTTTATTCG[A/T]GTTGGTACATATTCT | 286053 |
rs2384875 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218044 | TTGTTTATTCGAGTT[G/T]GTACATATTCTGCAT | 286053 |
rs2384876 | snp | G/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218068 | TCTGCATAATATCAG[G/T]ATGTGCATTATTAGT | 286053 |
rs2384877 | snp | G/T | 0.0850919 | 0.187897 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125164895 | ATTCAGTTATCTCCG[G/T]TTGAATAATTGTTTT | 286053 |
rs2384878 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243876 | CATCTTTTCTTTCAA[A/G]GAGCAACAGGGAAGA | 286053 |
rs2384879 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243913 | GTCACTGAAAAGACT[A/C]ACAACATATCCCACT | 286053 |
rs2384882 | snp | G/T | 0.135825 | 0.222405 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125178202 | CTGACCCAACAGGCA[G/T]CGAGAAAGACACTAC | 286053 |
rs2384883 | snp | A/G | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125114479 | GGGTATAGGCATGGA[A/G]TGCATATATAATCCA | 286053 |
rs2384884 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125114362 | CTTTCatttattgag[G/T]gcttactgtgaatca | 286053 |
rs2384885 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125114351 | tgagggcttactgtg[A/T]atcatgtacctatag | 286053 |
rs2384886 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125114335 | atcatgtacctatag[C/G]caataccagcgggta | 286053 |
rs2384887 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125114329 | tacctatagccaata[C/G]cagcgggtaagggta | 286053 |
rs2384888 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125114191 | aagtattaaacagtc[A/G]agagaaaaataaagc | 286053 |
rs2384889 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111820 | ATTATCAAGTAATTT[G/T]CAAACCAtttttttt | 286053 |
rs2384890 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111179 | CTGAAGTAACTGCCA[C/T]ACAGTGAAAACTTTT | 286053 |
rs2384891 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125096462 | TTCAGTGTAACCCAT[G/T]ATCTCATATATGATG | 286053 |
rs2384892 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125096536 | TTGAGTTTCTAGTGT[A/T]ATTTGTTTTTTTTTT | 286053 |
rs2384893 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125101460 | GATGTTTAGCAAGTC[C/T]TCCATGTTATGGTCC | 286053 |
rs2384894 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125101473 | CTCCATGTTATGGTC[C/T]ACCTGAATCCCATGA | 286053 |
rs2384895 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125101475 | CCATGTTATGGTCCA[C/T]CTGAATCCCATGAAA | 286053 |
rs2384898 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125103450 | ATTTGTGATGTGCCG[G/T]Ggtgtgatttttttt | 286053 |
rs2384899 | snp | A/G | | | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125129402 | ggaaattgaggccca[A/G]agagataaagtcact | 286053 |
rs2384900 | snp | A/G | | | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125129409 | gaggcccaaagagat[A/G]aagtcacttgtctaa | 286053 |
rs2384901 | snp | C/T | | | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125129463 | gtgcTTCTTCATTCC[C/T]ACTTAGTTTATTTGC | 286053 |
rs2384902 | snp | A/G | | | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125129530 | TGAAGATAGTGTTAG[A/G]AAAAGATTTGGCTCt | 286053 |
rs2384904 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125147368 | TATTGAAGGAAGAGC[G/T]TGATATAATTCTTTG | 286053 |
rs2384905 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125147371 | TGAAGGAAGAGCGTG[A/C]TATAATTCTTTGGTG | 286053 |
rs2384906 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125147384 | TGATATAATTCTTTG[G/T]TGGATCCTAAGAACA | 286053 |
rs2384907 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125147455 | TTGGTGAAAGGAAAC[A/C]AATGCAGATTAGAAA | 286053 |
rs2384908 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125147494 | TGGTGGTGGTCCCAA[A/G]ATATCAAAAGTGTAT | 286053 |
rs2384909 | snp | G/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125251459 | CTAAGTTTCCTCTTC[G/T]ACATTAATATGTTAA | 286053 |
rs2384912 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125251401 | TCACTGTCTCACCAT[C/T]AAGACCCGAGATATA | 286053 |
rs2384913 | snp | A/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125251392 | CACCATCAAGACCCG[A/T]GATATAATTTTCCAT | 286053 |
rs2384914 | snp | A/T | 0.4941 | 0.0539917 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125133125 | TATTAATTAGATTTT[A/T]AAAATCCATTTTAAA | 286053 |
rs2385092 | snp | A/G | 0.387832 | 0.208572 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125334735 | GCAGACTATGTGTAC[A/G]AAGGATTGGGCCAAA | 286053 |
rs2385093 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125334803 | tttttttttttttga[A/G]acacagtctcgctct | 286053 |
rs2385094 | snp | C/T | 0.295343 | 0.245854 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125344207 | TTTCAATTTGACTAA[C/T]TGAATAAACAAATCC | 286053 |
rs2385095 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125356870 | CAAGGCTGTAAAGCA[A/G]AGGCTTTAAAAAAGG | 286053 |
rs2891623 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125186823 | TTTACCATCCCCAGA[A/T]TACAAACCTAACAGA | 286053 |
rs2891626 | snp | A/C | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125210588 | AGTCTCTTTCTCTTT[A/C]TGGTCCATCTTACCC | 286053 |
rs2891627 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125162197 | TTTTGAAAAGCTGCA[A/G]CAATACTTCTCAGGA | 286053 |
rs2891628 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243930 | AACATATCCCACTTT[A/C/T]TGTATAAATCCCCCA | 286053 |
rs2891629 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125180634 | TAATGCTAAGACTCC[A/C]AGTTAGATACAGAAA | 286053 |
rs2891630 | snp | C/T | 0.4944 | 0.0526182 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125177849 | TTTAAAATGAGGGCA[C/T]TGGAAGAAAAAGAAG | 286053 |
rs2891631 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125147465 | GAAACCAATGCAGAT[A/T]AGAAAGGAAAGATTG | 286053 |
rs2891632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125147502 | GTCCCAAAATATCAA[A/G]AGTGTATGTGTTAAG | 286053 |
rs2891633 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125131077 | acttccttcagtgac[A/G]tttgtcatgcatttg | 286053 |
rs2891634 | snp | G/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125132437 | AGTGTGATAGCAGTG[G/T]TCTTGAATCCTAAGG | 286053 |
rs2891635 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125091156 | ATACTGATGTCAAAA[C/T]CCTTTGCATTTGGGG | 286053 |
rs2891677 | snp | C/T | 0.475259 | 0.108435 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125331966 | TTTCTCTAAGGAGAT[C/T]AAAGCTGCTTTGTGG | 286053 |
rs2891678 | snp | A/C | 0.46703 | 0.124089 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125349383 | AATAAGCATTTCAAG[A/C]AGGCAACAAATATTT | 286053 |
rs2954164 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125288863 | aggctgcagtgagcc[A/G]agatcgagccactgc | 286053 |
rs3763593 | snp | A/G | 0.137867 | 0.223442 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125093921 | TTGTCCTAGACCCTC[A/G]GAAGGCTGAGGTGGG | 286053 |
rs3812467 | snp | C/T | 0.19334 | 0.243495 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125290547 | AAAGAGGATACATAA[C/T]CTAGAATGCTATGAG | 286053 |
rs3923300 | snp | C/G | 0.206967 | 0.246268 | intron-variant, missense | NSMCE2 | GRCh38.p7 | 8:125130234 | GGGAAGAAGAGCACA[C/G]AGGTCAAGGGCCCTT | 286053 |
rs3955403 | snp | A/T | 0.0882987 | 0.190664 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217359 | tttatttatttattt[A/T]ttttttatttattta | 286053 |
rs3955404 | snp | C/T | 0.430285 | 0.173197 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125242017 | TGTGAGAACTGCTTC[C/T]TTAATGCCCCTTTTG | 286053 |
rs4006771 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252006 | TCAGACTCCAGACCA[C/T]ATTTCAATGGTTTAT | 286053 |
rs4006772 | snp | A/G | 0.451359 | 0.148171 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125251681 | GAAAATAACTATTCC[A/G]TTGTCTAAGACATAA | 286053 |
rs4006773 | snp | G/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125251433 | TTAATCATATTCAAG[G/T]CTCTCCCATTTAAAA | 286053 |
rs4006774 | snp | G/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125251310 | TTTCCAGTTCATTTG[G/T]GGGCATTTTCTGTAT | 286053 |
rs4006775 | snp | G/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125251065 | TCAGATCATTTGCAG[G/T]CCTACCATCAAAGAC | 286053 |
rs4006776 | snp | A/G | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125234369 | ctgaaaaatacagat[A/G]actgtcttaactcac | 286053 |
rs4006777 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125241094 | ttgaatatccctaat[C/G]tgaaaatctgaagtc | 286053 |
rs4006778 | snp | A/C | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125244078 | GACTAGCAGTTGTTA[A/C]CAGAGTGGTGTGCCA | 286053 |
rs4242367 | snp | A/G | 0.499396 | 0.0173617 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125290027 | TCATTTCCATTCAAG[A/G]GCAGAACATCAAAGA | 286053 |
rs4242368 | snp | C/T | 0.397271 | 0.202018 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125356998 | ACTTTAAAAAAGATT[C/T]TTTTTAACTGCTCTG | 286053 |
rs4278169 | snp | C/T | 0.0498117 | 0.149749 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217988 | AAGCAGAAGTCTCTA[C/T]GCTATTTTAATTGTT | 286053 |
rs4279612 | snp | C/T | 0.234692 | 0.249531 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125285145 | CTAAAACTAAAATGG[C/T]ACAGTTTGCTTTGGA | 286053 |
rs4294203 | snp | A/G | 0.234109 | 0.249494 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125281763 | tttttttttttttaa[A/G]gagatggggtcttgc | 286053 |
rs4300023 | snp | C/T | 0.494609 | 0.0516363 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125132007 | TCATGTCATGCATCC[C/T]TAGAGTTTCTCAGGT | 286053 |
rs4319117 | snp | C/T | 0.289165 | 0.246913 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125349522 | GCCTCAAGGGATCCT[C/T]CCACCTTGGCCTTCC | 286053 |
rs4330708 | snp | G/T | 0.4941 | 0.0539917 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125220957 | AACTTGGGCCCTGTG[G/T]GTGCTAAAAATATCT | 286053 |
rs4338125 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125240359 | tgaactcctgacctc[A/G]tgatcagcccgcctt | 286053 |
rs4339663 | snp | C/T | 0.287606 | 0.247155 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272792 | GTATATATATACACA[C/T]GTGTATATATATACA | 286053 |
rs4350000 | snp | A/G | 0.245916 | 0.249967 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125261583 | CTGGAAATTTAATTA[A/G]TATACTTACACTTTG | 286053 |
rs4360308 | snp | A/G | 0.134119 | 0.221521 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125190746 | ATAATACAGGTCATA[A/G]GCATGCTTTGTATAA | 286053 |
rs4367569 | snp | G/T | 0.446249 | 0.154875 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272864 | ACACACACATATATA[G/T]ACACACGTATACGTG | 286053 |
rs4372018 | snp | C/T | 0.469445 | 0.119766 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252474 | gagctcgcagtgagc[C/T]gagatcccgccactg | 286053 |
rs4464986 | snp | A/G | 0.279726 | 0.248226 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125285578 | TTACTTTAAACATGT[A/G]CATTTAGGTAACACT | 286053 |
rs4466418 | snp | C/T | 0.480302 | 0.0972668 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125311545 | ATATTGCACAACATA[C/T]CACGAATAAAGCATG | 286053 |
rs4477044 | snp | A/T | 0.174288 | 0.23826 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217328 | AACTGATCACTTTTT[A/T]AAAAAATTTTATTTA | 286053 |
rs4481615 | snp | G/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218417 | GAAAAATTGAGGGTT[G/T]TTTTTTTTTTTTGAG | 286053 |
rs4481616 | snp | A/G | 0.235564 | 0.249583 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298827 | GGATTAATTTAAAAA[A/G]TCACCCATCACCCTG | 286053 |
rs4503114 | snp | C/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298805 | ATCACCCTGCTTATT[C/T]TGAACCAATGTTGAC | 286053 |
rs4534140 | snp | C/T | 0.486984 | 0.079614 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272478 | ACCAAATGACTAACC[C/T]GGCACATGGGGACAG | 286053 |
rs4565472 | snp | A/G | 0.274124 | 0.248833 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125289744 | TCCTACTCAAGAAAG[A/G]AAACCTAAGCTTTAA | 286053 |
rs4601329 | snp | C/T | 0.161924 | 0.233971 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125242319 | GGAAGAAAAGCAATA[C/T]GGCAGCAACAGACAG | 286053 |
rs4602904 | snp | C/T | 0.362523 | 0.223246 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125302384 | ttgtcactcctggaa[C/T]gtgtgccaggccaac | 286053 |
rs4604453 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125240324 | GAGATGGGGTTTCAC[C/T]ATATTGGCCAGGCTG | 286053 |
rs4604454 | snp | A/G | 0.48818 | 0.0759629 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125267791 | AAAAAATAGTAATCG[A/G]TACTTTATCTAATAG | 286053 |
rs4870935 | snp | A/G | 0.48435 | 0.0870631 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125097014 | TTTTTCTGAATTTAT[A/G]TTTTTCCATCTTTTT | 286053 |
rs4870936 | snp | A/G | 0.47517 | 0.10862 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125325492 | gaagctggaaccaca[A/G]gcacataccaccaca | 286053 |
rs4870937 | snp | A/T | 0.469247 | 0.120128 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125325516 | caccacacctggcta[A/T]tttttttttattttt | 286053 |
rs4870938 | snp | A/G | 0.300169 | 0.244914 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125339580 | TAGTGTATCATAATG[A/G]ACATAATGAGGCATT | 286053 |
rs4871570 | snp | G/T | 0.141596 | 0.225274 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125105917 | CCAAAAAAGTTAATT[G/T]AAGAAAAATTTTGAG | 286053 |
rs4871571 | snp | A/G | 0.383632 | 0.211288 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125146725 | CACAGGAAGGGGAAC[A/G]TCACACACTGGGGCC | 286053 |
rs4871572 | snp | C/T | 0.494315 | 0.0530107 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125146734 | GGGAACGTCACACAC[C/T]GGGGCCTGTTGTGAG | 286053 |
rs4871573 | snp | A/G | 0.494692 | 0.0512434 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125146766 | TGGGGAGAGTGGGGA[A/G]GGATAGCCTTAGGAG | 286053 |
rs4871574 | snp | A/G | 0.49423 | 0.0534032 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125212275 | TATGACCTGTTTTCT[A/G]GTAGCCCAGGATAGA | 286053 |
rs4871575 | snp | A/G | 0.469445 | 0.119766 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125292413 | CACAAAATTAGTTGG[A/G]TGTGGTAGCACATGC | 286053 |
rs4871576 | snp | C/T | 0.468047 | 0.122292 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125292437 | CACATGCTTGTAATC[C/T]CAGCCACTTGGGAGG | 286053 |
rs4871579 | snp | A/G | 0.195837 | 0.244062 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125321541 | ccaaacattctacaa[A/G]gctagcattaccctg | 286053 |
rs4871580 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125321670 | atggaatccaaatat[A/G]tacaaaaaagataat | 286053 |
rs4871581 | snp | C/T | 0.205723 | 0.246048 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125323068 | TGTCTCAGAAAAATA[C/T]ATGTATATATGAAAT | 286053 |
rs4871582 | snp | G/T | 0.21875 | 0.248039 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125327700 | AAAAGTAAGATTTCT[G/T]TAGAATATTACAGGA | 286053 |
rs4871583 | snp | A/G | 0.195837 | 0.244062 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125350587 | tggggaggcctcaca[A/G]tcatggcagaagaca | 286053 |
rs4871584 | snp | C/G | 0.380138 | 0.213458 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125351130 | GCAACTCGGTGGATG[C/G]TGACTGAGAAGAGGA | 286053 |
rs4871588 | snp | A/G | 0.207559 | 0.246371 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125365142 | CTCAGTCTCTCTTCT[A/G]GGAGGGCTACTGGGC | 286053 |
rs5007394 | snp | A/T | 0.494484 | 0.0522255 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125205826 | TAATAAAATATGCTA[A/T]CTCTGATGGTCAAGC | 286053 |
rs5894750 | in-del | -/T/TTTTC | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125240131 | TCTTTTTTTTTTTTT[-/T/TTTTC]GAGACGGAGTCTTGC | 286053 |
rs5894752 | snp | G/T | 0.303938 | 0.244112 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298697 | TGTGGGttttttttt[G/T]ttttttttttttttt | 286053 |
rs6415489 | snp | A/G | 0.494855 | 0.0504572 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125215175 | tagttatatctccca[A/G]tgctatccctccccc | 286053 |
rs6415490 | snp | A/G | 0.227959 | 0.249026 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125277664 | GGCACCCGCCACCAC[A/G]CCTGGCTAATTTTTG | 286053 |
rs6470338 | snp | A/T | 0.4944 | 0.0526182 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125120893 | CAGACATGTATGCCT[A/T]GACTAAAGTTGAGAG | 286053 |
rs6470339 | snp | G/T | 0.494651 | 0.0514399 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125149226 | ATATTTGTGTATTCT[G/T]TGCTGCCTGGATAGT | 286053 |
rs6470341 | snp | C/T | 0.384976 | 0.210431 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125178635 | cagcactttgggagg[C/T]ggaggcgggcggatc | 286053 |
rs6470342 | snp | A/G | 0.494609 | 0.0516363 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125191137 | TCGGCCTCCCAAAGC[A/G]CTGGGATTACAGGTG | 286053 |
rs6470343 | snp | A/G | 0.448452 | 0.152042 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125199221 | tcttgccttctgcta[A/G]ctttagaatttgttt | 286053 |
rs6470344 | snp | A/T | 0.4944 | 0.0526182 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125223480 | gacataccaatttca[A/T]ttcatttgtatgtat | 286053 |
rs6470346 | snp | C/T | 0.348354 | 0.22984 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125277760 | ACCTTGTGATCCACC[C/T]GCCTCGGCCTCCCAG | 286053 |
rs6470347 | snp | A/G | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125280216 | GTTAGAAGAGTTACA[A/G]CTCCCTCTTCCCTGC | 286053 |
rs6470348 | snp | C/T | 0.17461 | 0.238362 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125289632 | TGTCTGACATGGCTC[C/T]GCTTATTAAATGTTT | 286053 |
rs6470349 | snp | A/G | 0.213333 | 0.247296 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125313992 | TCTGGCATTTCCAGG[A/G]TAGTTATTTAGAATA | 286053 |
rs6470350 | snp | A/G | 0.475965 | 0.106957 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125315303 | TGTTCCTTTACCTCA[A/G]AGCCCCAGCTTCCAC | 286053 |
rs6651233 | snp | C/T | 0.376592 | 0.215579 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125278360 | TAGGTTTGCTTGCCA[C/T]GCTGTCTGGTTCCTT | 286053 |
rs6651234 | snp | A/C | 0.135143 | 0.222054 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125326062 | ggagatcgagaccat[A/C]ctggataacatggtg | 286053 |
rs6651235 | snp | A/G | 0.122411 | 0.214991 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125326130 | ggtgcggtggcaggc[A/G]cctgtagtcccagct | 286053 |
rs6651236 | snp | A/G | 0.197082 | 0.244335 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125358282 | aggttgcagtgagcc[A/G]agattgtgccactgc | 286053 |
rs6651237 | snp | G/T | 0.135143 | 0.222054 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125358637 | TCGTTTGGCATTTCT[G/T]GTGCTCTTATCATGG | 286053 |
rs6981550 | snp | C/T | 0.373397 | 0.217424 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125345412 | CACTATTTTCATCTT[C/T]TTATTGTGGTAAATT | 286053 |
rs6981647 | snp | A/G | 0.160938 | 0.233598 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125236488 | AGTATATAAATTTAT[A/G]TGTATATATAAATGT | 286053 |
rs6983240 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125097382 | AGGCTGTCTACACTA[C/T]ATTCCCAAAGAATGA | 286053 |
rs6984563 | snp | C/G | 0.101301 | 0.200969 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125249410 | GAATCCCTTTCTCAC[C/G]TACATGCAGTCTTTG | 286053 |
rs6984812 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125367505 | GGGCGACAGAGCAAG[A/C]CTCTAAAAAAAAAAA | 286053 |
rs6984988 | snp | C/G | 0.243061 | 0.249904 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125124482 | gatttctctctctct[C/G]tctctctctctctct | 286053 |
rs6985382 | snp | C/T | 0.175576 | 0.238665 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125270357 | gtaaacccagctact[C/T]gggaggctaagacat | 286053 |
rs6985411 | snp | A/G | 0.229429 | 0.249152 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125300535 | AGAGATTAAAAAGTT[A/G]TGGTATCTCAGTAAG | 286053 |
rs6985519 | snp | C/G | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125300488 | CATTTAGACCTCGTT[C/G]TAAGCCATATCAAAT | 286053 |
rs6986059 | snp | A/T | 0.478354 | 0.101757 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125315853 | CGTCACCCAGGCTGT[A/T]GTGCAGTGGTGCAGT | 286053 |
rs6986712 | snp | C/T | 0.478437 | 0.10157 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316270 | CTCAATTCAGAACAA[C/T]TCACCTTCTATATAT | 286053 |
rs6987612 | snp | A/C | 0.0410537 | 0.137264 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125107018 | aaacaacaaaaaaaa[A/C]ctttcattttaccat | 286053 |
rs6987626 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125107038 | cattttaccattagc[A/G]acaaatgctgttagt | 286053 |
rs6987716 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125106869 | agcgtggtggtgggc[A/G]cctataatcccggct | 286053 |
rs6988465 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125225243 | CAGAGAGGCACTGTG[A/G]GGCCATGCCAAGAAA | 286053 |
rs6988747 | snp | A/G | 0.236434 | 0.249632 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125160436 | GATAGGCTGAAGGAA[A/G]GGCCTCTTTCCTCGG | 286053 |
rs6988871 | snp | A/T | 0.146985 | 0.227789 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125091345 | ATCCATACAGCAGTG[A/T]TCCCGGAAACTTGGA | 286053 |
rs6989375 | snp | G/T | 0.375 | 0.216506 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298694 | ATCTGTGGGtttttt[G/T]ttgtttttttttttt | 286053 |
rs6989383 | snp | C/T | 0.47517 | 0.10862 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125330681 | TAAGCCTCGAATGTA[C/T]GCTAGGTACTAAAGG | 286053 |
rs6989407 | snp | A/G | 0.381308 | 0.21274 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125330781 | GAGTGATGATCACCC[A/G]ACATTGCCTCCCACA | 286053 |
rs6989594 | snp | G/T | 0.130351 | 0.219509 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125291625 | GTGTTTTCAGTGTGA[G/T]GGAAAGATTGTTTCC | 286053 |
rs6990622 | snp | A/G | 0.475259 | 0.108435 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125331321 | TAAAAAATAATAATA[A/G]TAATAATTTTAAAAA | 286053 |
rs6991820 | snp | A/G | 0.237593 | 0.249692 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125268353 | GTCACTGGCACTTCT[A/G]TTGGTCGTTTGAAGG | 286053 |
rs6992378 | snp | A/G | 0.0637235 | 0.166737 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201218 | tgttccattgctggc[A/G]aggagctgtgatccg | 286053 |
rs6992389 | snp | A/G | 0.0637235 | 0.166737 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201233 | gaggagctgtgatcc[A/G]ttggaggagaagagg | 286053 |
rs6992463 | snp | A/G | 0.490007 | 0.0699769 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125255765 | TTGCATTTTGGATTG[A/G]AGCTGTCtgatcagg | 286053 |
rs6992545 | snp | C/T | 0.242488 | 0.249887 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125160640 | CAATGAAAAAGATAC[C/T]GCACCCTTTAATATG | 286053 |
rs6994510 | snp | A/G | 0.195214 | 0.243923 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125314512 | GGCCAGGCTGGTCTC[A/G]AACTCCTGACTTCGT | 286053 |
rs6995023 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125183907 | AAAAGACCGAGAACT[A/G]TTCTATTTGGTGCTT | 286053 |
rs6995096 | snp | A/G | 0.47614 | 0.106587 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125096143 | tttactaaggtccct[A/G]tgcttgcctgcatca | 286053 |
rs6995274 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125183817 | TAGAAACTCTGATTG[A/G]CAGCTTTCGATTTCT | 286053 |
rs6995986 | snp | A/G | 0.487241 | 0.0788465 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125268822 | ATGGCCAGCAGTGCC[A/G]GAGCCTGCAGATCAA | 286053 |
rs6997136 | snp | C/G | 0.242488 | 0.249887 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125179169 | TTCTAAGTCCTGTAT[C/G]TGGGTAGACTTTATT | 286053 |
rs6997329 | snp | A/G | 0.167484 | 0.23599 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125262158 | Aggccgggtgcgatg[A/G]ctcacacctgtaatc | 286053 |
rs6997418 | snp | G/T | 0.243061 | 0.249904 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125193004 | TGATATTATTTGTAA[G/T]TAATATATTAACAAC | 286053 |
rs6997485 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125239567 | tgaaccaagatcatg[C/T]cactgcactctagcc | 286053 |
rs6997658 | snp | A/G | 0.239037 | 0.24976 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125232246 | TGCATGCCTGTAATC[A/G]CAGCTACTCGGGAGG | 286053 |
rs6997862 | snp | C/T | 0.312104 | 0.242163 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125108610 | TATGCTAAGTGCTCT[C/T]AGCCACAATGTTAAT | 286053 |
rs6998191 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125172524 | AAATATGCTCTCCCC[C/G]TCCCCAAAAGGGGGA | 286053 |
rs7000553 | snp | A/T | 0.493925 | 0.054776 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125215016 | tttggtaaccacttt[A/T]ttttattttatttta | 286053 |
rs7001448 | snp | A/G | 0.0633504 | 0.166319 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125245436 | CAAGTCAAAGGCTAC[A/G]TCAAAACTATAGTTA | 286053 |
rs7002224 | snp | A/G | 0.301932 | 0.244547 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125172730 | TTATGTCAGACCAAA[A/G]AATAAATATGAATAG | 286053 |
rs7002315 | snp | G/T | 0.119281 | 0.213102 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125262831 | GAATCAAATGAAATG[G/T]TGGTTTTGAAAGAGC | 286053 |
rs7003102 | snp | A/G | 0.379158 | 0.214052 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125291251 | TGGTAATCATAAAAG[A/G]TTCCGTTTACATTTT | 286053 |
rs7004396 | snp | A/G | 0.112631 | 0.208878 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125228342 | TAATTGGTTAGAATA[A/G]AAGAAGAAAAGTATG | 286053 |
rs7004468 | snp | A/G | 0.18197 | 0.240566 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316186 | CATGTCTTCTTTTTC[A/G]ATTCTAGTCTCCTAA | 286053 |
rs7004739 | snp | A/G | 0.477937 | 0.102688 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316141 | TGCATGATGATAACA[A/G]ATGCCATCCCAGGGC | 286053 |
rs7004753 | snp | A/G | 0.478437 | 0.10157 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316174 | ACAAGTGAATAGCAT[A/G]TCTTCTTTTTCAATT | 286053 |
rs7007866 | snp | A/G | 0.324619 | 0.238604 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125291605 | ATCAGATGATACACC[A/G]GGATGTGTTTTCAGT | 286053 |
rs7008046 | snp | C/G | 0.278664 | 0.248351 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125291772 | AGCAAGCCAGATCTC[C/G]TAAACAATAATTAAC | 286053 |
rs7008482 | snp | G/T | 0.490007 | 0.0699769 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125255388 | CAATGACAGTGATAT[G/T]TACTACGTATCACAG | 286053 |
rs7009033 | snp | C/T | 0.323908 | 0.238825 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125258934 | TGAGACAGAGTTTTG[C/T]TCTTGTTGCCCAGGC | 286053 |
rs7010240 | snp | G/T | 0.475259 | 0.108435 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125331161 | AAAAATTAGCCGGAC[G/T]TGGTGGCAGGCGCCT | 286053 |
rs7010333 | snp | A/G | 0.390464 | 0.206809 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125340392 | TTCTTGGCCGTCTTT[A/G]TATTACTTCTGAAAA | 286053 |
rs7010385 | snp | A/G | 0.304438 | 0.244001 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125229499 | TGCCAGGAAGAAAGG[A/G]TGGAAGAGAATCTGA | 286053 |
rs7010394 | snp | C/T | 0.47517 | 0.10862 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125331278 | GCACTCCAGCCTGGG[C/T]GACAGAGCGAGACTC | 286053 |
rs7010813 | snp | C/T | 0.188316 | 0.242271 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125246810 | tacaacttgatgttt[C/T]gatatagatataaat | 286053 |
rs7010992 | snp | A/C | 0.245346 | 0.249957 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125246959 | tttcaaaccaatctc[A/C]agtatactatataat | 286053 |
rs7011185 | snp | C/T | 0.23031 | 0.249223 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271524 | AGCCTTTGGTTATCT[C/T]GGACATGAAGGATTA | 286053 |
rs7014707 | snp | C/T | 0.301429 | 0.244653 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125165017 | CTGTATGTGGCATTA[C/T]ATGGGACATGTAAAA | 286053 |
rs7015295 | snp | C/G | 0.232359 | 0.249377 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125104994 | tgccactgtactcca[C/G]cctggggaagagagt | 286053 |
rs7015414 | snp | C/T | 0.463559 | 0.129972 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125339188 | CTCAATTTTCTCTCC[C/T]CAGCTTACAGTTCTC | 286053 |
rs7015753 | snp | A/G | 0.475348 | 0.108251 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125318565 | GTATACAGTGATGTT[A/G]ATGGCAACATCTATT | 286053 |
rs7015929 | snp | C/T | 0.186105 | 0.241697 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125311305 | TCACTCAGTTCTCTG[C/T]TTCATTTAAAACCTA | 286053 |
rs7016484 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125187610 | AGCAATCTTTCTGGC[A/G]TCTTTTATTCATTTA | 286053 |
rs7016677 | snp | A/C | 0.304188 | 0.244057 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125210854 | GCCTCCCCAGTAGCT[A/C]GGACTACAGGTATGT | 286053 |
rs7016773 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125335828 | TAAGAACTAGGCATT[A/G]CTCAACCAAAGGGGA | 286053 |
rs7016797 | snp | A/T | 0.471388 | 0.116136 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125269098 | TTTGTTTTTTGTTTG[A/T]TTTTTTGAGACAGAG | 286053 |
rs7017478 | snp | C/T | 0.494187 | 0.0535994 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125232186 | ACCAACATGGAGAAA[C/T]CCCGTCTGTACTAAA | 286053 |
rs7017497 | snp | C/T | 0.242201 | 0.249878 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125172042 | ACCTACATTAATTCA[C/T]TTAATACTCAAAGGT | 286053 |
rs7017794 | snp | C/T | 0.230017 | 0.2492 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125262494 | TCCTTTAGTTTGCCA[C/T]TCATTCATTCATCCa | 286053 |
rs7018048 | snp | A/G | 0.0126979 | 0.078662 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125093479 | ggatcacttgaggtc[A/G]ggtgtttgagaccag | 286053 |
rs7357374 | snp | C/T | 0.244205 | 0.249933 | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125090546 | TATATTTTCTTATTT[C/T]CTTTTACAAGTGCCG | 286053 |
rs7357375 | snp | C/T | 0.438806 | 0.163867 | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125090578 | TAACTTCATTTTTAA[C/T]AATTTGGCGTGGAAC | 286053 |
rs7387525 | snp | A/G | 0.462909 | 0.131034 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125297764 | cacttgagcccagga[A/G]tttgaggctacagtg | 286053 |
rs7460712 | snp | C/G | 0.186421 | 0.24178 | intron-variant, utr-variant-5-prime | NSMCE2 | GRCh38.p7 | 8:125130161 | tgttttgtagaatgt[C/G]tctcagctggagttt | 286053 |
rs7461265 | snp | C/G | 0.0524604 | 0.153226 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125177922 | CAGTTTCAGTGATTT[C/G]TGCTGCTTTCCTCAA | 286053 |
rs7461756 | snp | A/G | 0.386123 | 0.209692 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125125955 | cagatttttgtaacg[A/G]gcagtaaacttccct | 286053 |
rs7464613 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217441 | tctcagctcactgca[A/T]gctctgcctcccagg | 286053 |
rs7812392 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125266177 | gctcaccgcaacctc[C/T]gcctcccaggttcaa | 286053 |
rs7812492 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125266182 | ccgcaacctccgcct[C/T]ccaggttcaagagat | 286053 |
rs7812530 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125266252 | atgtgccaccacgcc[C/T]ggctaattttgtgtt | 286053 |
rs7812636 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125266162 | caatgcgcgatctcc[A/G]ctcaccgcaacctcc | 286053 |
rs7812682 | snp | C/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125266323 | GTCTATTTTTTAAAC[C/T]CCATCAAACTGTAGA | 286053 |
rs7812775 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125266217 | ctgcctcggcctccc[G/T]agtagttgggattac | 286053 |
rs7812802 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125266265 | cccggctaattttgt[A/G]tttttagtagagatg | 286053 |
rs7812933 | snp | A/C | 0.234401 | 0.249513 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125294177 | acatttcattatatg[A/C]atataccacatttta | 286053 |
rs7813225 | snp | A/G | 0.494774 | 0.0508504 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125165769 | CAGTTTTTTGATTAG[A/G]CTTGTGATGGATAGA | 286053 |
rs7813432 | snp | A/G | 0.281577 | 0.247998 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125294347 | gctgggtcatatggt[A/G]actctatgtttatcc | 286053 |
rs7814063 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125288998 | agatggtcagtgttg[A/T]ccaggctggtctcaa | 286053 |
rs7814242 | snp | C/G | 0.0633504 | 0.166319 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125166302 | agacagagtctcgct[C/G]tgtcaccaggctgga | 286053 |
rs7815471 | snp | C/T | 0.47517 | 0.10862 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125329603 | CTGTCTAGCTTGTTC[C/T]GATATACTGGGACAA | 286053 |
rs7816350 | snp | A/G | 0.233527 | 0.249457 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125277363 | AGGCACTAGAGGCAC[A/G]ATGACTAAATAATAT | 286053 |
rs7816430 | snp | C/T | 0.494442 | 0.0524218 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125148593 | TGGTTTTGGGGTACC[C/T]CTAATCAGCAGAATT | 286053 |
rs7816900 | snp | A/G | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125266684 | TTCATGAGAATTTCA[A/G]ATCCAGTATACCTGT | 286053 |
rs7817794 | snp | A/T | 0.496583 | 0.0411924 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125200111 | cagcacattgttggg[A/T]cttgactctttatcc | 286053 |
rs7818322 | snp | A/T | 0.341235 | 0.232758 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125286319 | ACCTTTTATTTATTT[A/T]TTTTTTTTTTTGAGA | 286053 |
rs7818760 | snp | C/T | 0.38286 | 0.211774 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125312581 | agtgagccaagatca[C/T]gccactgcattccag | 286053 |
rs7819612 | snp | C/T | 0.373799 | 0.217195 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125364235 | AGGTGTGAGCCACCG[C/T]GCCTGGCCATATTTT | 286053 |
rs7820192 | snp | C/T | 0.0718919 | 0.175435 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125124715 | actcctggggtcaag[C/T]gatcctcctgccttg | 286053 |
rs7820297 | snp | C/T | 0.499741 | 0.0113788 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125277620 | CACGCCATTCTCCTG[C/T]CTCAGCCTCCCGAGT | 286053 |
rs7820336 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125337900 | AAAAAAAAAAAAAAA[A/G]AAAAAGAAAGAAAGA | 286053 |
rs7820471 | snp | C/T | 0.381308 | 0.21274 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125337964 | GGAGTCATTTTTCTG[C/T]TTCTTTTTAAGATAG | 286053 |
rs7820489 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298693 | CATCTGTGGGttttt[G/T]tttgttttttttttt | 286053 |
rs7822467 | snp | A/T | 0.142272 | 0.225598 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125309744 | aaaaaaTGTATTAAT[A/T]GTTCAAATTTCCATG | 286053 |
rs7822592 | snp | A/G | 0.466927 | 0.124269 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125356133 | agattgaatgcatac[A/G]cagatatccaaatcc | 286053 |
rs7822618 | snp | C/T | 0.243347 | 0.249911 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201066 | ttctagttagtcatt[C/T]gtctaaccttttttc | 286053 |
rs7822970 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125164479 | ATTTTGTACATCTCT[C/T]ATTGTAAATTTTCCA | 286053 |
rs7823012 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125164576 | AGAGAGGGATTCTAT[G/T]AGAATTAAGGAACTA | 286053 |
rs7823372 | snp | C/T | 0.242201 | 0.249878 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125192392 | GTGCGTGGTGTGTTA[C/T]TGTGTGTATAGCAAG | 286053 |
rs7823958 | snp | A/G | 0.293551 | 0.246177 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125343841 | TCCACTAAAAAATAA[A/G]AAAAATAAAAAAAAA | 286053 |
rs7824458 | snp | C/T | 0.0663309 | 0.169604 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125284148 | aacagagcgagactc[C/T]ggaaaaagaaaaaaa | 286053 |
rs7824635 | snp | C/T | 0.19646 | 0.2442 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125344441 | TCTTTTTTCTATATA[C/T]CATTGTTTAAGATGA | 286053 |
rs7825799 | snp | C/T | 0.187053 | 0.241946 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125244154 | ACTAATAGCAGGGAT[C/T]TACAATTATAGAATG | 286053 |
rs7826327 | snp | C/T | 0.0759472 | 0.179459 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272177 | caccatcatgcctgt[C/T]gaatttttttgtatt | 286053 |
rs7827336 | snp | A/C | 0.301681 | 0.2446 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125144153 | GGTACCATGTACTAC[A/C]GGACCTGTTTCATCT | 286053 |
rs7827795 | snp | A/G | 0.277867 | 0.248442 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125262206 | tgaggcaggtggatc[A/G]caaggtcaggagatt | 286053 |
rs7827809 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125320200 | agagagagagagaga[A/G]agaaaGAgaaggaag | 286053 |
rs7828199 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125320186 | atctcaaaaaaaaaa[A/G]agagagagagagaaa | 286053 |
rs7828200 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125320188 | ctcaaaaaaaaaaga[A/G]agagagagagaaaga | 286053 |
rs7828222 | snp | A/G | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125320222 | agaaggaaggaagga[A/G]ggagggagggaaggg | 286053 |
rs7831515 | snp | C/T | 0.494651 | 0.0514399 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125120574 | TAAACTAGTTTCTTA[C/T]GATATTGGGCAAGCC | 286053 |
rs7831918 | snp | C/T | 0.171057 | 0.237209 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125288624 | CTCTCACTTTGGTTG[C/T]TGTTACTGTTGACAT | 286053 |
rs7833107 | snp | A/T | 0.255224 | 0.249945 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125106494 | accagcctgaccaac[A/T]tggtgaaaccccatc | 286053 |
rs7833463 | snp | C/T | 0.242488 | 0.249887 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125188583 | AGATTTTAAAAACAC[C/T]GTTCAAACAAAACTG | 286053 |
rs7834583 | snp | C/T | 0.148326 | 0.228391 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316453 | ACACTACTGGCAGTA[C/T]GTGCATTGGTCAGAA | 286053 |
rs7835561 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125120939 | TTGAATTTACCCTTC[C/G]CTCTTCATTCTACTG | 286053 |
rs7835771 | snp | A/T | 0.473543 | 0.111932 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355040 | GAAATTCATGTTTAG[A/T]CTTGGGTCCCATCCC | 286053 |
rs7836427 | snp | A/T | 0.4944 | 0.0526182 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125115669 | GGCAGGAGAATTGCT[A/T]GAACCAGGTGGGTGG | 286053 |
rs7836506 | snp | C/T | 0.494484 | 0.0522255 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125115588 | AAACCCCATCTCTGC[C/T]AAAAATACAAAAATT | 286053 |
rs7836761 | snp | C/G | 0.494442 | 0.0524218 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125115626 | CATGGTGGCAGATGT[C/G]TGTAATCCCAGCTAC | 286053 |
rs7837793 | snp | A/G | 0.0539704 | 0.155153 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125352219 | ggcgtggtggctcac[A/G]cctgtaatcccagca | 286053 |
rs7837996 | snp | A/G | 0.236434 | 0.249632 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125204346 | TTCCTTGCCCAGTTT[A/G]ACCATTGGGTCCTTC | 286053 |
rs7838563 | snp | C/T | 0.499203 | 0.0199521 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125277635 | CCTCAGCCTCCCGAG[C/T]AGCTGGGACTACAGG | 286053 |
rs7839038 | snp | A/G | 0.0633504 | 0.166319 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125164269 | CCTCAAGAAGGTTAA[A/G]GGACTTGCGCAGATC | 286053 |
rs7839274 | snp | C/T | 0.242775 | 0.249896 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125192210 | TAAGAAAATAATTAT[C/T]TTGTTGAGTTATAAT | 286053 |
rs7839468 | snp | C/G | 0.0633504 | 0.166319 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125164554 | CCACACTGATGTGGC[C/G]TGTGTTAGAGAGGGA | 286053 |
rs7839693 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125151618 | ATTTGCTTAAACATA[C/G]AATTGAGACCAGGTT | 286053 |
rs7840065 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125186851 | AGATATACTACACTC[A/C]TTTAGAGATACTGTT | 286053 |
rs7840900 | snp | C/T | 0.111576 | 0.20818 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201058 | actgtttattctagt[C/T]agtcattcgtctaac | 286053 |
rs7841947 | snp | C/T | 0.373196 | 0.217538 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125313687 | CCCATGTATGTGTTA[C/T]ACACGTCCTTAGAGT | 286053 |
rs7841990 | snp | A/G | 0.174288 | 0.23826 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125265242 | ttttttctttttgaa[A/G]cggagtttcactctt | 286053 |
rs7842181 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125139939 | GTAGTTTCTCCTCAG[A/G]TGTAGATGTTTTTAA | 286053 |
rs7842852 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125164756 | GTAAAATAAAAATGA[A/G]ATAAACTTTTTTCTA | 286053 |
rs7843098 | snp | C/G | 0.232359 | 0.249377 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125293505 | AATTTATTTGAACTT[C/G]GTTCAATAAATGATC | 286053 |
rs7844453 | snp | A/G | 0.232359 | 0.249377 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125105447 | TTTGAAGATTCCTGG[A/G]AGTTTTAGCTACAGA | 286053 |
rs7844459 | snp | C/T | 0.23031 | 0.249223 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272167 | TACAGGCGCCCACCA[C/T]CATGCCTGTCGAATT | 286053 |
rs7844497 | snp | A/G | 0.373799 | 0.217195 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125341342 | ATATTTTCCTGTAGA[A/G]TTCATAAAGCAAGTT | 286053 |
rs7845165 | snp | A/G | 0.355311 | 0.226737 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125275646 | ATGTTTTATGTAGGG[A/G]CCTCTAGCCACTTCA | 286053 |
rs7846609 | snp | C/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125266029 | CAAAATCCTGTGACC[C/T]GAATAAAGAACACAT | 286053 |
rs9297712 | snp | A/T | 0.494057 | 0.0541878 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125208657 | GTGCCAGCGTAAGTG[A/T]TTCATACAATTAACA | 286053 |
rs9297714 | snp | A/G | 0.281049 | 0.248064 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125294391 | CCAGACTTTTCCAAA[A/G]GGACTGCGCCATTTT | 286053 |
rs9297715 | snp | A/G | 0.0763149 | 0.179815 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125296001 | TTTATTAAAGTATGA[A/G]TAGGAATTACAGCTT | 286053 |
rs9297716 | snp | A/G | 0.499622 | 0.0137383 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125342920 | TAGATTTGCACCCTC[A/G]GGCTTTGATCTTTTT | 286053 |
rs9671173 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196920 | gagatggtatctcat[A/T]gtggttttgatttgc | 286053 |
rs9694656 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125320204 | agagagagagaaaga[A/G]agagaaggaaggaag | 286053 |
rs9886469 | snp | C/T | 0.477768 | 0.103061 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125349579 | CATAGTGAGAGCTTG[C/T]ATTTAAAAAAAAAAA | 286053 |
rs9987342 | snp | A/G | 0.230017 | 0.2492 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125101061 | ATGAGTTGTACTGTG[A/G]ATGTTTGAGGTAAAC | 286053 |
rs10016168 | snp | A/C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196705 | GATTTGTAGTCCTTT[A/C/G]GGTACATACCCAGTA | 286053 |
rs10086862 | snp | A/G | 0.278664 | 0.248351 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125285658 | ACAGCAACATGTGAA[A/G]ACAGTACAAGAATCT | 286053 |
rs10087220 | snp | A/T | 0.0592355 | 0.161582 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125242075 | AATCACTGTGTCTAA[A/T]GGAAGTGTATCTCTA | 286053 |
rs10088227 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125097871 | ATTATATTGTAGAAA[A/G]CTTTGGATACTGTGC | 286053 |
rs10088674 | snp | A/G | 0.0763149 | 0.179815 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304263 | ttacatgaataatat[A/G]tataaagatcctacc | 286053 |
rs10089963 | snp | C/T | 0.303938 | 0.244112 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125195035 | TCACCTAGAAACTTA[C/T]TAAAAATATAAATTT | 286053 |
rs10090093 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125195156 | TTGAGAACCACTGGT[C/T]TACAGCGGAGGTGCT | 286053 |
rs10090347 | snp | A/G | 0.0850919 | 0.187897 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125264487 | GCTCGGCTTACTGCA[A/G]TCTCTGCCTCCTGGG | 286053 |
rs10091027 | snp | A/G | 0.491104 | 0.0660973 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252109 | attgcccaggagagt[A/G]tagtcagcaaaaaga | 286053 |
rs10091741 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125287315 | tcagcctgggtgaca[A/G]agtgaaactctgtct | 286053 |
rs10091742 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125287317 | agcctgggtgacaga[A/G]tgaaactctgtctca | 286053 |
rs10093274 | snp | C/G | 0.469445 | 0.119766 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125264653 | ACCTCAGGTGATCAG[C/G]GTGGGCTGTTCTTGA | 286053 |
rs10093674 | snp | G/T | 0.0919752 | 0.193722 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125283607 | ACTGCTTAATTAACC[G/T]CTGTGAATATCAATA | 286053 |
rs10093813 | snp | C/T | 0.303938 | 0.244112 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125205021 | ATTTCACTTTCTCAC[C/T]GCTCTCCTCTCTAGC | 286053 |
rs10093819 | snp | A/G | 0.304438 | 0.244001 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125140133 | TGTTAGAATTTTTCA[A/G]CCGTATGCTTGATTA | 286053 |
rs10094316 | snp | C/T | 0.494692 | 0.0512434 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125138561 | AATTGACAAGACCAG[C/T]GTGTGATCAGGTAGT | 286053 |
rs10094940 | snp | A/G | 0.0663309 | 0.169604 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125347814 | AGATAGCTTCACCAC[A/G]TACATAGAATCTGAG | 286053 |
rs10095101 | snp | A/G | 0.163236 | 0.234461 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125223042 | actccagcctgggca[A/G]cagagtgagaccctg | 286053 |
rs10095360 | snp | A/T | 0.401658 | 0.239953 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125278991 | AAGCATATTAAATAT[A/T]TTGTGTTTGTATAAT | 286053 |
rs10096127 | snp | A/C/T | 0.0592355 | 0.161582 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125247908 | ggtgaactaaagtga[A/C/T]cactttccttgtgaa | 286053 |
rs10096522 | snp | A/G | 0.262159 | 0.249704 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125153036 | cactccagcctgggc[A/G]acagagcgagactcc | 286053 |
rs10097568 | snp | C/T | 0.304188 | 0.244057 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196679 | gtgtgcatgtgtctt[C/T]acggtagcatgattt | 286053 |
rs10097806 | snp | A/G | 0.0670745 | 0.170406 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125206131 | GCAGTATAAATATTT[A/G]TATGTATTCTGATCA | 286053 |
rs10098862 | snp | A/G | 0.171704 | 0.237423 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125193860 | GTGAGAAGCAGCCTC[A/G]TAATTACCCTTTGTT | 286053 |
rs10099782 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125248733 | AATGAGACTCACTAA[C/T]ATTtttcaagtgtat | 286053 |
rs10100121 | snp | A/G | 0.475259 | 0.108435 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125336888 | AGTCCTATTGGCAAC[A/G]TAGGCATTCATCCAT | 286053 |
rs10100523 | snp | A/G | 0.0722614 | 0.17581 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125359855 | AGGCATGGGAGACGA[A/G]GACAGTTTTAAAGGA | 286053 |
rs10100556 | snp | A/G | 0.494526 | 0.0520291 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125189227 | ACAGATGGAATAATG[A/G]CAAGAGCACACCTGA | 286053 |
rs10100566 | snp | C/G | 0.476052 | 0.106772 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125336990 | AATATCCCAACATCT[C/G]ATCCTCTTGCCTTTT | 286053 |
rs10101223 | snp | A/G | 0.0748431 | 0.178382 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125330279 | tctcccggttcgagc[A/G]attctcctgcctcag | 286053 |
rs10101690 | snp | A/G | 0.281577 | 0.247998 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125294675 | CATAGTTCTTTACAA[A/G]ATGAATGTCATTTAT | 286053 |
rs10102769 | snp | A/G | 0.172351 | 0.237636 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125137073 | TTTGCTATTATTTTC[A/G]TGAAATCAAAATTTT | 286053 |
rs10103776 | snp | A/G | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125283400 | AAAAATTAGCTGCTC[A/G]TGGTGACCTGCACCT | 286053 |
rs10104659 | snp | C/T | 0.475259 | 0.108435 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125331027 | AGAAAGGTGACTGGG[C/T]GCGGTGGCTCACACC | 286053 |
rs10105404 | snp | A/G | 0.0667028 | 0.170006 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125142863 | cgcctcagcctccca[A/G]agtgctgggattaca | 286053 |
rs10105823 | snp | A/G | 0.0663309 | 0.169604 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125200958 | cttccagttgatcga[A/G]tcgggtattgaagct | 286053 |
rs10105854 | snp | A/G | 0.47517 | 0.10862 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125326160 | TACTCGGGAGGCTGA[A/G]GCAGGAGAATGGCGT | 286053 |
rs10106359 | snp | A/G | 0.47517 | 0.10862 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125326302 | AAATCAAGTCATCCT[A/G]TATGTGTCAATAGGA | 286053 |
rs10106726 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125222555 | ctctggtaaccacca[C/T]gctattctcaaagtc | 286053 |
rs10106909 | snp | C/T | 0.162581 | 0.234218 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125216725 | ACTGTCTGAAAAATC[C/T]CCTGCTTCAACCATT | 286053 |
rs10106942 | snp | C/T | 0.49614 | 0.0437598 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125098808 | gggggagGGGTAGGG[C/T]GGGAGAGAAGGAATG | 286053 |
rs10106955 | snp | C/G | 0.0667028 | 0.170006 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125171483 | AGTTCCTAATCAATA[C/G]CATAGGATGTATTCA | 286053 |
rs10107857 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125155771 | GGTTTGGAGAGTGAA[C/T]ACCAGTTTAGTTCAG | 286053 |
rs10107980 | snp | G/T | 0.0670745 | 0.170406 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125210403 | CCTGAAAGAGAGAGC[G/T]CATTGAGGGTGATGA | 286053 |
rs10108110 | snp | C/G | 0.381308 | 0.21274 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125331641 | CACTTTTCTCTTAAT[C/G]CTTCAGAATAGCACA | 286053 |
rs10108305 | snp | A/C | 0.347694 | 0.230122 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125278899 | CCAGGATTCAACTCA[A/C]ACCGAGAACCAGGAT | 286053 |
rs10108634 | snp | C/T | 0.0759472 | 0.179459 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125279149 | TCAAAAAGGACATTC[C/T]ACTCTTATTACAAAG | 286053 |
rs10109490 | snp | A/G | 0.164546 | 0.234942 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125144001 | GATATCTGGTAGTGT[A/G]ATGAAGTAGTATAGA | 286053 |
rs10109574 | snp | A/G | 0.163236 | 0.234461 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125171750 | GACCATAAGAATACC[A/G]GTAATAATAATAGCA | 286053 |
rs10110582 | snp | A/T | 0.084364 | 0.187256 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125131723 | TGGGATGTATATTTT[A/T]AAAATGCAAAATTGG | 286053 |
rs10110845 | snp | C/T | 0.449853 | 0.150196 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125247892 | GTGCTAGTGAACAAG[C/T]GGTGAACTAAAGTGA | 286053 |
rs10110958 | snp | C/T | 0.162909 | 0.23434 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125219800 | AAAACACCACACCAA[C/T]TGAAAAATCACTGTG | 286053 |
rs10111234 | snp | C/T | 0.111576 | 0.20818 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125132217 | attcttccacctcag[C/T]ttcctgagtagctgg | 286053 |
rs10112218 | snp | A/T | 0.494484 | 0.0522255 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125148078 | GTTCTTTTTAGAATT[A/T]CCTTCCTGATCTCTT | 286053 |
rs10112583 | snp | C/T | 0.247905 | 0.249991 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111014 | GCTCTTCTTTGCAGC[C/T]GGTTACAGTCCTGAC | 286053 |
rs10112737 | snp | C/T | 0.487558 | 0.0778863 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125273084 | CTTCATAAATGGTTG[C/T]TGTTACTTTTATTCT | 286053 |
rs10149280 | snp | C/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196619 | ATGGGCATTTGAGTT[C/T]ATTCCAATCTTTGCT | 286053 |
rs10216374 | snp | G/T | 0.47517 | 0.10862 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125330132 | AAGGATGGAAACAAG[G/T]CTGCCTTCTTGTTAG | 286053 |
rs10216523 | snp | A/T | 0.303938 | 0.244112 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125178152 | AGTAATCATTTTTTT[A/T]AAACTCTCATTATCA | 286053 |
rs10216768 | snp | A/G | 0.47517 | 0.10862 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125330232 | CCCAGGCTGGAGTGC[A/G]ATGGGACGATCTAGG | 286053 |
rs10283134 | snp | A/G | 0.483126 | 0.0902898 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125260404 | ATTACAGTGTAGGGC[A/G]GTTCATTTTGATTCA | 286053 |
rs10283200 | snp | C/T | 0.48155 | 0.0942576 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125260618 | TCCCTAATTTCATTT[C/T]ATTTATTTATTTATT | 286053 |
rs10481079 | snp | A/G | 0.0748431 | 0.178382 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125307291 | TTCCAGGAGCAGTCT[A/G]GGAAGATAGCTGAAA | 286053 |
rs10481153 | snp | A/G | 0.0763149 | 0.179815 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125296242 | CACCCTTAACTCCCA[A/G]CACTCACTTCTGCTG | 286053 |
rs10481154 | snp | C/T | 0.0748431 | 0.178382 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125305647 | AAAGAGAAACAGACC[C/T]TCAGTAAATGAAGGC | 286053 |
rs10505453 | snp | A/G | 0.47517 | 0.10862 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125332651 | TCCAGATATATTACA[A/G]GTTTTCTTTTAAACA | 286053 |
rs10505454 | snp | A/G | 0.212425 | 0.24716 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125332834 | ACCCTGTGAGAAGCC[A/G]TTTAGTCTTATGAAC | 286053 |
rs10550331 | in-del | -/CA | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125285779 | acacacacacacaca[-/CA]aagctatacacacag | 286053 |
rs10558922 | in-del | -/TTTTTA | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125315815 | TTTTTTTCCCTCTCT[-/TTTTTA]AAGTCAGGGTTTCAC | 286053 |
rs10564130 | in-del | -/CA | 0.111928 | 0.208413 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125285757 | TTCTTCATACACACG[-/CA]CACACACACACACAC | 286053 |
rs10578122 | in-del | -/TG | 0.37138 | 0.218556 | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125129545 | GAAAAGATTTGGCTC[-/TG]TGTGTGTGTGTGTGT | 286053 |
rs10609215 | in-del | -/TT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125183350 | ATCATGATGAGACTT[-/TT]GTTTTTACTGTAGAC | 286053 |
rs10635586 | in-del | -/AT | 0.474992 | 0.108989 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272699 | TCCCAGCTACTTGGG[-/AT]ATATATATATATATA | 286053 |
rs10635587 | in-del | -/AC | 0.287346 | 0.247195 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272846 | TATACACACGTATAT[-/AC]ACACACACACATATA | 286053 |
rs10654840 | in-del | -/AAAAT/AAAATAAAAT/AAAATAAAATAAAAT | 0.534044 | 0.141374 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125262096 | GTGAGACTCTGTCTC[lengthTooLong]AAAATAAAATAAAAT | 286053 |
rs10755926 | snp | A/G | 0.499872 | 0.0079862 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125297061 | AATTAAATTGTTACA[A/G]TCACTTCACTGGGCC | 286053 |
rs10808543 | snp | A/G | 0.366266 | 0.221319 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125366118 | CCCTGAGTCCAGCCA[A/G]TGAAGCTGTGGCCCC | 286053 |
rs10930904 | snp | A/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196593 | TCCGTCAATGATAGA[A/T]TGGATTAAGAAAATG | 286053 |
rs10956233 | snp | C/G | 0.481856 | 0.0935034 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252764 | AGAATGAAAGCATAC[C/G]TTTAACTTGTATAAG | 286053 |
rs10956234 | snp | A/G | 0.288386 | 0.247035 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125263351 | TACTCAGTTATACCT[A/G]CTGGCTCATGGAACA | 286053 |
rs10956235 | snp | G/T | 0.273224 | 0.264661 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125263665 | TGAGGCAGGACAATC[G/T]CTTGAACCCGGGAGG | 286053 |
rs10956236 | snp | G/T | 0.27893 | 0.24832 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125270869 | gaacagccactgcac[G/T]ccaaccagggcaaca | 286053 |
rs10956237 | snp | C/T | 0.470811 | 0.117228 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125283969 | CCATCCTGGCTAACA[C/T]GGTGAAACCCCGTCT | 286053 |
rs10956238 | snp | G/T | 0.499187 | 0.0201513 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125299023 | AGGTAGCACATTTCA[G/T]GAATAGTTGATGCTA | 286053 |
rs10956239 | snp | C/T | 0.475081 | 0.108804 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125317488 | AGGCGTGCACCACCA[C/T]ACCTGACCAAGATTC | 286053 |
rs10956240 | snp | A/G | 0.475348 | 0.108251 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125319579 | GTAAAGACCCAATAa[A/G]atgaaacctacaatg | 286053 |
rs10956241 | snp | A/G | 0.47517 | 0.10862 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125326645 | TTATAAGTTTAAAAA[A/G]AAGATTGGTTAAAAA | 286053 |
rs11284016 | in-del | -/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125315112 | TCATTGACTAGAATC[-/T]TTTTTTTTTCTTTTT | 286053 |
rs11292879 | in-del | -/A | 0.495855 | 0.045338 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125108034 | GCCAGAGCCTGTCTC[-/A]AAAAAAAAATAAAAA | 286053 |
rs11299819 | in-del | -/A | 0.409721 | 0.192325 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125262929 | TTCAGTGCCTCCGCG[-/A]AAAAAGGTTGAAGAT | 286053 |
rs11336684 | in-del | -/T | 0.324619 | 0.238604 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125361068 | TGCCTTATGATTTCC[-/T]TTTTTTTTTTTTCGT | 286053 |
rs11343986 | in-del | -/T | 0.494484 | 0.0522255 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125169732 | AAAGTGAACATTTGA[-/T]TTTTTTTTTCCTGCC | 286053 |
rs11345496 | in-del | -/T | 0.304438 | 0.244001 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125170099 | CATAGCATTTGTAGC[-/T]GTAACCTAGTCCTCT | 286053 |
rs11359401 | in-del | -/A | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125349584 | TGAGAGCTTGTATTT[-/A]AAAAAAAAAAAAAAA | 286053 |
rs11365667 | in-del | -/T | 0.270351 | 0.24917 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125282116 | AATGTCATCCCTTAA[-/T]TTTTTTTTTTTCTTT | 286053 |
rs11389668 | in-del | -/A | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125344742 | TCAAAAAAAAAAAAA[-/A]GAAAAGAAAATTAAT | 286053 |
rs11389676 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125183412 | TTTGTTCTTTTTTTT[-/T]AACATCACAGCTCCC | 286053 |
rs11403131 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125286793 | AAAAAAAAAAAAAAA[-/A]TTGCCCAAAGCCAAT | 286053 |
rs11407395 | in-del | -/T | 0.198014 | 0.244535 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125244031 | AAGATATTGTAAGAG[-/T]TTTTTTTTTTAAGTA | 286053 |
rs11410793 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125296393 | TTGTTGCCATGGTCA[-/T]TTTTTTTTTTTTTTT | 286053 |
rs11411074 | in-del | -/A | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125338284 | GAAAAAAAAAAAAAA[-/A]GCTGCCTTTTATATA | 286053 |
rs11440819 | in-del | -/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125330196 | TTTTTTTTTTTTTTT[-/T]GAGACAGTCTCTCTC | 286053 |
rs11453416 | in-del | -/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125315798 | GGTACCCTTTTTTTT[-/T]CCCTCTCTAAGTCAG | 286053 |
rs11542104 | snp | C/T | 0.00486615 | 0.0490856 | missense | NSMCE2 | GRCh38.p7 | 8:125151210 | TGGACAAGGCAATGG[C/T]TGAATTTGCTACATT | 286053 |
rs11542888 | snp | A/C | 0.0133922 | 0.0807265 | utr-variant-5-prime, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125091666 | ACTGGGTGCCGGCTC[A/C]GCGCGCGACCTCCGG | 286053 |
rs11774053 | snp | C/T | 0.475259 | 0.108435 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125321543 | aaacattctacaagg[C/T]tagcattaccctgat | 286053 |
rs11774940 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125299565 | acccagttacctccc[A/C]ccaggtccctccctc | 286053 |
rs11776254 | snp | A/G | 0.477768 | 0.103061 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125348556 | TCCCATAATTCCCAC[A/G]TGTTGTGAGAGGGCC | 286053 |
rs11777625 | snp | C/T | 0.475437 | 0.108066 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125321400 | ggaattatactgttt[C/T]aaggctcttacacta | 286053 |
rs11777731 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125324866 | ggcatgagccaccgc[G/T]cccggcccattttga | 286053 |
rs11778001 | snp | G/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125150715 | CATTAGGAAGATTGG[G/T]CCAAATAATCTAGCT | 286053 |
rs11778488 | snp | A/T | 0.0189856 | 0.0955633 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243502 | AAATAATAATTTTTT[A/T]AAAAAAAAAACCTCT | 286053 |
rs11778683 | snp | C/T | 0.47517 | 0.10862 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125325947 | acaagagtgaaactc[C/T]gtctcaaaataaata | 286053 |
rs11778726 | snp | A/G | 0.47517 | 0.10862 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125325929 | tgtactccagcctgg[A/G]caacaagagtgaaac | 286053 |
rs11778987 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125107989 | caatgagctgagatc[A/T]cacgactgtactcca | 286053 |
rs11779422 | snp | C/G | 0.388964 | 0.20782 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271768 | CTGTTTTTCACTCAT[C/G]CTTTTTAATGACTCT | 286053 |
rs11782629 | snp | A/G | 0.475348 | 0.108251 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125322926 | tagctgggtgtggtg[A/G]cgcatgcctgtgatc | 286053 |
rs11785165 | snp | G/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125274347 | AATCAATGTTCCTTG[G/T]ATTAATTTCATTTTA | 286053 |
rs11786188 | snp | C/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125174674 | TTAAGCTTATTCATT[C/T]TCACAATTTTTCCGA | 286053 |
rs11985468 | snp | G/T | 0.0759472 | 0.179459 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125282904 | ATTATGGATGGAAAC[G/T]ATGAGAATCGTTCTG | 286053 |
rs11986135 | snp | C/T | 0.494013 | 0.0543839 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125122172 | GTTCTCTGGCTGAGC[C/T]AAAAAAAAAAAAAAA | 286053 |
rs11987320 | snp | A/C/T | 0.00938946 | 0.0678717 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125147710 | GCAGGGAGCCTCTGC[A/C/T]TGATCAGTACCTCCA | 286053 |
rs11987707 | snp | C/T | 0.147991 | 0.228242 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125253740 | AGCTTAAAATGAAGT[C/T]GTATAGGCAGCCTGA | 286053 |
rs11988647 | snp | C/T | 0.0752113 | 0.178743 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125295451 | GTGCTTAGGATTTCT[C/T]AGAAATCTCCCCAGA | 286053 |
rs11990560 | snp | A/G | 0.0755793 | 0.179102 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125289974 | AAAGCTGGTGTACAC[A/G]TGTGATAGTGTTTTT | 286053 |
rs11990593 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125239555 | cagaggttgcagtga[A/T]ccaagatcatgccac | 286053 |
rs11991576 | snp | C/T | 0.168135 | 0.236216 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125253993 | GCTTCTCAAAAGGCC[C/T]AGAAGATAACAAATA | 286053 |
rs11993019 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125340059 | tcgctctgtggccca[G/T]gcgggagtgcagtgg | 286053 |
rs11994181 | snp | C/G | 0.0733688 | 0.176922 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125365813 | agtgagctgagatca[C/G]gccactgcaccccag | 286053 |
rs11994861 | snp | A/G | 0.44638 | 0.154709 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125254002 | AAGGCCTAGAAGATA[A/G]CAAATATTTGTCTAA | 286053 |
rs11995477 | snp | G/T | 0.0678174 | 0.1712 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125233570 | CAATTATTTTAAGGT[G/T]TTTATGCATGCTTGA | 286053 |
rs11995484 | snp | A/G | 0.494733 | 0.0510469 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125212477 | CAGACTATTGTGGGA[A/G]CCTCTTGAACAACAA | 286053 |
rs11996045 | snp | A/G | 0.0726307 | 0.176182 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125343154 | TAAATCCTATGGGGC[A/G]ACATATTTGATTAGA | 286053 |
rs11997581 | snp | A/G | 0.47517 | 0.10862 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125326849 | TAATCCCAACTACTC[A/G]GGAGACTGAGTCAGG | 286053 |
rs11998130 | snp | G/T | 0.0596104 | 0.162024 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125241211 | tcagattaaggatac[G/T]gaacctgAATTTGGA | 286053 |
rs11998251 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125244837 | GAGTAAATGAACATT[C/T]GCACACAAAAAAAGA | 286053 |
rs12056336 | snp | A/G | 0.241914 | 0.249869 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125215612 | gatccctgaggaatc[A/G]cctatgtcctgaatg | 286053 |
rs12114619 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125364140 | gtaaagatagggttt[C/T]gccatgttggccagg | 286053 |
rs12115051 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125184408 | TTCCTCAGGCCACCA[A/G]TACACATTATTTGGA | 286053 |
rs12381058 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196695 | atagcagcatgattt[A/G]tagtcctttgggtac | 286053 |
rs12381061 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196749 | gtcaaatggtatttc[C/T]agttctagatccctg | 286053 |
rs12541675 | snp | C/T | 0.205417 | 0.245993 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125343161 | TATGGGGCGACATAT[C/T]TGATTAGATTCGGGG | 286053 |
rs12542512 | snp | G/T | 0.336474 | 0.234568 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125293475 | TATTTACTGACTCCA[G/T]TGGGTTAATTTTGAA | 286053 |
rs12542709 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125247624 | cagctactcgggagg[C/T]tgaggcaggagaatc | 286053 |
rs12542820 | snp | C/T | 0.494484 | 0.0522255 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125187954 | TTTAGGTCACTGTTA[C/T]ATATAGAATATATGG | 286053 |
rs12544110 | snp | G/T | | | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125090845 | AACAAAATATAACGG[G/T]TGCTGATCAAGATAA | 286053 |
rs12544146 | snp | A/G | 0.184838 | 0.241358 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125160098 | AGAGACAATAAAAAC[A/G]TGCATAGGAAATTCA | 286053 |
rs12545259 | snp | A/G | 0.212425 | 0.24716 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125320069 | tagtcccacctgctc[A/G]ggaggctgcggcagg | 286053 |
rs12545690 | snp | A/G | 0.0614824 | 0.164198 | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125089872 | GCAATAGTAAAACAA[A/G]TATTATGGGTCTTTA | 286053 |
rs12545710 | snp | A/C | 0.45843 | 0.138046 | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125089956 | TTTTAATGCAAAAGC[A/C]TATGAGTTATATTTA | 286053 |
rs12545844 | snp | A/G | 0.203267 | 0.245593 | intron-variant, downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125363512 | TCAAAAAAAGAAAGA[A/G]GAAAGAGGAGAGAAA | 286053 |
rs12546048 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125173215 | ATCAGTGGAGGTATT[A/G]TTGAGTCCCTTGGTG | 286053 |
rs12547610 | snp | A/G | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125105221 | agttattcatttacg[A/G]ctaacagcaggtgtc | 286053 |
rs12549738 | snp | A/G | 0.475348 | 0.108251 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125314204 | CCATTAAAAGCTTAT[A/G]CAAATCCCATAAATC | 286053 |
rs12550607 | snp | A/G | 0.482979 | 0.0906686 | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125089830 | TTAAAAGAACATGAG[A/G]AGGATAATAATAACC | 286053 |
rs12675647 | snp | A/T | 0.134119 | 0.221521 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125283957 | aggagatggagacca[A/T]cctggctaacatggt | 286053 |
rs12675943 | snp | A/G | 0.216048 | 0.247684 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125247850 | TTATTACTAAGACAA[A/G]TTGTAATATTACTCT | 286053 |
rs12676352 | snp | C/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125214829 | TCGtgtattaacatt[C/T]atattacataaaact | 286053 |
rs12679295 | snp | C/T | 0.242488 | 0.249887 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125164284 | GGGACTTGCGCAGAT[C/T]ACTTGGTTAGTCTCA | 286053 |
rs12679602 | snp | A/G | 0.189576 | 0.242588 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125275298 | CTCACACTTCATCCC[A/G]TCTTCTAGCCCTCTC | 286053 |
rs12679991 | snp | A/C | 0.00999975 | 0.0699991 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125281373 | ATAAAAGTTCAGTCA[A/C]TAAATGACTAAAATT | 286053 |
rs12680080 | snp | A/T | 0.131723 | 0.220251 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125296882 | CTAATTTTTTTCTCT[A/T]AAGAAATTAGAATAA | 286053 |
rs12680560 | snp | C/T | 0.475259 | 0.108435 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125333254 | GGCTCACTGCAGCTT[C/T]GACCTCCTGGGCCCA | 286053 |
rs12680754 | snp | C/T | 0.191147 | 0.242974 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125242291 | TAACATATTTGATCC[C/T]GTAGAATCAAAGGGA | 286053 |
rs12681565 | snp | C/T | 0.236434 | 0.249632 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125164466 | AAGTATATTTATGAT[C/T]TTGTACATCTCTTAT | 286053 |
rs12681602 | snp | A/G | 0.221141 | 0.248329 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125255778 | tgaagctgtctgatc[A/G]ggtttgtgttttaga | 286053 |
rs12682185 | snp | A/G | 0.243061 | 0.249904 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125131791 | ACAAGCATCCCAAGT[A/G]ATTCTGATACATCCT | 286053 |
rs13248099 | snp | C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298229 | tgtgccactgcactc[C/G]agcctgggtgacagt | 286053 |
rs13248183 | snp | A/C | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298334 | taagttaactcattg[A/C]tcctgaccacagccc | 286053 |
rs13248194 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298343 | tcattgatcctgacc[A/C]cagccctttgaggca | 286053 |
rs13248409 | snp | A/C | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298341 | actcattgatcctga[A/C]cacagccctttgagg | 286053 |
rs13249982 | snp | A/G | 0.385359 | 0.210185 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125189443 | AAGGTTTAAGGCTAA[A/G]ACTTGCCTGGGCCTG | 286053 |
rs13250502 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298332 | tttaagttaactcat[A/T]gatcctgaccacagc | 286053 |
rs13251643 | snp | A/T | 0.0217236 | 0.101931 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125228526 | gggaagacttcctgg[A/T]agagctgacatttga | 286053 |
rs13253942 | snp | A/G | 0.123105 | 0.215401 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125142407 | TTACTGTATTACATC[A/G]TCTCTCTTCTGTGTC | 286053 |
rs13253991 | snp | A/C | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125166718 | GGGAAGACACTTCTG[A/C]TACCATCTAGTTGGG | 286053 |
rs13254173 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125325396 | cactctgtcacccag[G/T]ttggagtgcagtggc | 286053 |
rs13254815 | snp | C/T | 0.477684 | 0.103247 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125364334 | AAACTCCTTGATCCA[C/T]AGATCAGGGCCAAGA | 286053 |
rs13254947 | snp | A/G | 0.135825 | 0.222405 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125186342 | TGACTTTTTACAGTA[A/G]ATGTTTACTGACCCT | 286053 |
rs13255114 | snp | C/T | 0.4776 | 0.103433 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125364457 | TTACTGTGGTTTGCA[C/T]ATTTGTTGTTTTTGG | 286053 |
rs13255528 | snp | G/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125112292 | acccttgtgtattgt[G/T]ggtgcgaatgtaaat | 286053 |
rs13259062 | snp | C/T | 0.123452 | 0.215605 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125163616 | GTTTTGACTACCCCC[C/T]TGCCCCACAAAATTG | 286053 |
rs13259646 | snp | C/T | 0.476314 | 0.106217 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316608 | TTTCTTTCCTTCTTT[C/T]CTTTCTTTATTTCCT | 286053 |
rs13259995 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316764 | ttccttccttccttc[C/T]ttccttctctctctc | 286053 |
rs13260816 | snp | A/G | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271332 | GTTAAGATACTATCA[A/G]AGTGGACATAAAGGG | 286053 |
rs13260832 | snp | A/G | 0.116138 | 0.211142 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125317088 | CACCACTCCTGGCCT[A/G]TTGTTTCTGATTTCA | 286053 |
rs13261064 | snp | A/C | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271383 | AACAATTAAATTTGA[A/C]AGATATTTGGAATGT | 286053 |
rs13261579 | snp | C/T | 0.476227 | 0.106402 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125340146 | CAGCCTCCCGAGTAG[C/T]TGGGACTACAGGCGC | 286053 |
rs13261587 | snp | C/T | 0.47614 | 0.106587 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125340155 | GAGTAGCTGGGACTA[C/T]AGGCGCCCGCCATCA | 286053 |
rs13261980 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316695 | ttcttatcttccttc[C/T]ttccttccttccttc | 286053 |
rs13261993 | snp | C/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316711 | TTCCTTCCTTCCTTC[C/T]TTCCTTCTTTCTTTC | 286053 |
rs13262004 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316719 | TTCCTTCTTTCCTTC[C/T]TTCTTTCCTTCTTTT | 286053 |
rs13262006 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316723 | TTCTTTCCTTCTTTC[C/T]TTCCTTCTTTTCCTT | 286053 |
rs13262218 | snp | A/G | 0.499121 | 0.020948 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125287265 | TGAACCTGTTAGGTA[A/G]AGGTTGCAGTGAGCT | 286053 |
rs13262348 | snp | C/T | 0.141596 | 0.225274 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125104527 | aatttgagtgtctcc[C/T]ggtcctaggtcctac | 286053 |
rs13263406 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125167628 | aactgagcaagactc[A/G]gtctcaaaaaaaaaa | 286053 |
rs13264500 | snp | C/T | 0.154329 | 0.23097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125200847 | tgtcacatagtccca[C/T]atttcttggaggctt | 286053 |
rs13264577 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304883 | acagagccagactct[G/T]aaaaaaaaaaaagag | 286053 |
rs13264639 | snp | A/G | 0.21875 | 0.248039 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304956 | AAGGAAGGAAGGAAG[A/G]AAGAAAGAAAGAAAA | 286053 |
rs13265319 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125256083 | ggtcaagagatcaag[A/C]ccatcctggccaaca | 286053 |
rs13265348 | snp | C/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125334773 | ATGAAGTATCTTTTC[C/T]ttttttttttttttt | 286053 |
rs13266756 | snp | C/T | 0.0685596 | 0.171987 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125255804 | ttagacaaatccttc[C/T]atcagcagtggggaa | 286053 |
rs13266794 | snp | C/G | 0.385932 | 0.209815 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125138459 | TCGAACTTCTGGCCT[C/G]AAGTGATCCTCCTGC | 286053 |
rs13267325 | snp | C/T | 0.122758 | 0.215196 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125117106 | CTTTTTTCTTGATTA[C/T]TTTATAATATAGTTA | 286053 |
rs13271521 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125296683 | ttacagatgtgagtc[A/C]ccgcacccggccTGC | 286053 |
rs13273034 | snp | A/G | 0.137187 | 0.223099 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125122754 | AGTTGTATTTCAACT[A/G]TATACTATATATATT | 286053 |
rs13273063 | snp | C/G | 0.47517 | 0.10862 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125327259 | CGATAAAGCAAGACT[C/G]CATCTCAAAAAAAAA | 286053 |
rs13273231 | snp | C/T | 0.136166 | 0.22258 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125135274 | caggttggtctcaaa[C/T]tcctggccttaggtg | 286053 |
rs13273421 | snp | C/T | 0.123105 | 0.215401 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125179330 | TGACAGAGCCCGACC[C/T]TGTCTCTTAATTTAA | 286053 |
rs13274361 | snp | C/T | 0.475348 | 0.108251 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125319757 | cagggcaccagtgaa[C/T]tgtgggacagtctca | 286053 |
rs13277490 | snp | C/T | 0.135484 | 0.22223 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125141010 | GCCAAAGGGGGTCTG[C/T]GGATATGCTTTAAAA | 286053 |
rs13277691 | snp | A/G | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125140937 | GACAAGAAAGATGTG[A/G]AAAAAAGATAAGTCA | 286053 |
rs13278949 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125175686 | TCCTGTGATCTCCCC[C/T]CCCAGTGAAACGATG | 286053 |
rs13278971 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125110760 | TAATTTTGGTTGTTG[G/T]TGttttttttttttt | 286053 |
rs13278973 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125110763 | TTTTGGTTGTTGTTG[G/T]ttttttttttttttt | 286053 |
rs13279146 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125206412 | AGGAAAGCAAGTCTG[A/G]TTGTGGTATATAGGA | 286053 |
rs13279210 | snp | G/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125140935 | TGGACAAGAAAGATG[G/T]GGAAAAAAGATAAGT | 286053 |
rs13281548 | snp | C/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125166567 | ccaccgcgcctggcc[C/T]TAAATAGATTTTTTA | 286053 |
rs13282876 | snp | A/C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298225 | agattgtgccactgc[A/C/T]ctccagcctgggtga | 286053 |
rs16900402 | snp | A/G | 0.0879971 | 0.190408 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125160485 | TGGGGTATGGAAGTT[A/G]GTGCTCATAGTCAGT | 286053 |
rs16900403 | snp | C/G | 0.0836354 | 0.186609 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125162450 | TGGTCCTGTTACAAT[C/G]GTAAATTTTCCAGTG | 286053 |
rs16900405 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125163980 | TGGAGTTTGTTTCAA[A/G]TATGTTGGAGGCCTT | 286053 |
rs16900408 | snp | C/T | 0.0498117 | 0.149749 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125164277 | AGGTTAAGGGACTTG[C/T]GCAGATCACTTGGTT | 286053 |
rs16900409 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125164776 | ACTTTTTTCTAGTTT[C/T]AATGATATGGTTTAT | 286053 |
rs16900426 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125203412 | CTTTTACTGAGAAAT[A/G]AGCCACATGGCTCCA | 286053 |
rs16900427 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125203476 | CCCATGCTTCATCCT[A/G]CCCCTACCTTGTAAA | 286053 |
rs16900431 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125204586 | ATTTGATAGTTGTAT[A/G]GAGTCAAGAAAATAT | 286053 |
rs16900439 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125208391 | TATAGGAATAGAGAA[A/G]AAGAAACATGGGACA | 286053 |
rs16900444 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125211043 | TGGCCTCCCAGATTG[A/G]TTTCATTCCCACTAC | 286053 |
rs16900446 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125214397 | CCAGGAAATCCATGA[A/G]CATTAAAGGAATGAG | 286053 |
rs16900447 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125220042 | TTCATTGGTTTTGAA[A/G]GGCAGACCAAACCCA | 286053 |
rs16900450 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125226147 | TTTTCTTGGCATATT[A/G]AACTGACATTGGGCA | 286053 |
rs16900452 | snp | A/G | 0.133777 | 0.221342 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125230858 | CTTAGACAGCAGGGG[A/G]CAGCAGCATGAGATA | 286053 |
rs16900454 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125233008 | GTAACTAGTTCTGGA[G/T]GCTTAGTTACGCAAT | 286053 |
rs16900455 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125233169 | TCCAGCTAGGCAACA[C/T]AGGTATGTAATTTAG | 286053 |
rs16900457 | snp | A/G | 0.239037 | 0.24976 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125235918 | ACCTAGTAGGTAAGA[A/G]TCCACATTTTACATA | 286053 |
rs16900461 | snp | G/T | 0.0799831 | 0.183287 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125236588 | CACTAAACTACTGAC[G/T]GAGGCCATCTCTGAG | 286053 |
rs16900462 | snp | A/G | 0.251014 | 0.249998 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125238554 | TGCACTGTTAGCTGG[A/G]ACTTCATTAAACAGC | 286053 |
rs16900463 | snp | G/T | 0.0479149 | 0.147179 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125238847 | GTTTATGTATACAAT[G/T]GGAGTTCTGCAGTAA | 286053 |
rs16900464 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125239129 | GGCAAGGTTGGTTTC[A/G]TGGACTGAGCCACTC | 286053 |
rs16900465 | snp | A/C | 0.0221141 | 0.102801 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125241718 | TAGTGGTGATTTTAA[A/C]AAAAGTACTCATAGT | 286053 |
rs16900466 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125242959 | AACCTAAAAGTTTAT[A/G]TCAAAAACCCACAAC | 286053 |
rs16900469 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250543 | TACTTGTTTCACTTA[C/T]ATTCTCATGAATTCA | 286053 |
rs16900479 | snp | G/T | 0.146985 | 0.227789 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125255686 | GGTTGAATCATGAAG[G/T]CCCGTGTTTGCCAGG | 286053 |
rs16900487 | snp | C/T | 0.10237 | 0.201756 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125261102 | AAAATTACTGTTTTG[C/T]GAATCAACCAAAGTA | 286053 |
rs16900488 | snp | A/C | 0.485731 | 0.0832509 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125262586 | TAGGGTAGCAAGAAT[A/C]AATAAGACAGTCAGA | 286053 |
rs16900491 | snp | A/G | 0.120674 | 0.21395 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125264085 | TCTGAATTTTCTCCA[A/G]CGAACATAGAGACAA | 286053 |
rs16900500 | snp | C/T | 0.17332 | 0.23795 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125275189 | TCCTTTTCCTGTCCA[C/T]AGGAGAATGTCTTTC | 286053 |
rs16900502 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125275250 | CTTTGATGCAACTCT[C/G]ATTTCAGCTTCTGTG | 286053 |
rs16900508 | snp | A/G | 0.0475351 | 0.146656 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125276527 | AGAATAATTAATAAT[A/G]GAATAGCCTCATTTG | 286053 |
rs16900510 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125279778 | TATCTCCTTAGTGGA[C/T]GGATTGCTTGTTAAG | 286053 |
rs16900516 | snp | A/C | 0.326035 | 0.238157 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125289825 | CAGTTAGCAGTTGTT[A/C]ATCACACTAGCTGAT | 286053 |
rs16900525 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125293195 | TATTATACTCATGTC[C/T]GGGAAATAGGATGCT | 286053 |
rs16900535 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125303667 | CCAATTGCTGTACAG[A/T]AATTCAACTCCACAT | 286053 |
rs16900538 | snp | G/T | 0.197082 | 0.244335 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125305931 | AGTACAGGCTAAATG[G/T]TATTTTAGGGTGCTG | 286053 |
rs16900559 | snp | A/G | 0.206336 | 0.246157 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125340594 | AATGAAATAGTCATT[A/G]GCTTTTTTGTCATTA | 286053 |
rs16900568 | snp | G/T | 0.194902 | 0.243853 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125353300 | TACTCTTAAACACAC[G/T]ATCAGAAATGGGAGG | 286053 |
rs17310558 | snp | C/G | 0.135143 | 0.222054 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125226913 | ACTTGTTCTGGCAAC[C/G]CTCTGCCTCATCTTT | 286053 |
rs17311104 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125254308 | GGATTTGAGTCATTA[C/G]TGTGCCACAAAACAT | 286053 |
rs17318327 | snp | C/T | 0.113334 | 0.209338 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125303675 | TGTACAGAAATTCAA[C/T]TCCACATACTCAACA | 286053 |
rs17318886 | snp | C/T | 0.0596104 | 0.162024 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125334684 | TGTCTTGAAATGAGG[C/T]GGTTAGAGCTCAGAG | 286053 |
rs17319046 | snp | G/T | 0.0444908 | 0.142359 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125338552 | CTTTTCTGAATTTCG[G/T]TAGCAGTAGCAACAA | 286053 |
rs17319374 | snp | A/G | 0.0539704 | 0.155153 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125349438 | ATAGTTTCAAGAGAA[A/G]AGTGCTTTTAGGAAA | 286053 |
rs17401283 | snp | A/T | 0.135484 | 0.22223 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125168089 | ATTTTTGAAATCACT[A/T]ATCGATGGGTTTAAT | 286053 |
rs17401491 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125206538 | TGCAAGAAGTGTTGT[A/G]GAAGTAGTATCTATA | 286053 |
rs17402478 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125261220 | CTATTATGCTGGATA[A/C]TATGGGAGCAAGTTT | 286053 |
rs17403327 | snp | C/T | 0.181022 | 0.240296 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125312190 | TAATAAACTTTGATG[C/T]CTCTGTTCTATGCTT | 286053 |
rs17403341 | snp | C/G | 0.122064 | 0.214785 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125313586 | CTTAGCTCTTTTGTT[C/G]TCACCTTCCACATAA | 286053 |
rs17404103 | snp | A/G | 0.0539704 | 0.155153 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125347003 | TCAGAGGAGTGTGTC[A/G]AAAGAGCCATGGAAG | 286053 |
rs28374689 | snp | A/G | 0.0763149 | 0.179815 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125289199 | TCATACTTACTTCCT[A/G]GAGTAATCAGAACAC | 286053 |
rs28412398 | snp | G/T | 0.0763149 | 0.179815 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125288007 | ATCTCTGTTTTTCTT[G/T]TGGAGACAGGGTCTC | 286053 |
rs28439379 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125159548 | GGTTTGTGTAAGTAC[A/C]CTCCGTGATGTTCCA | 286053 |
rs28446973 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125314292 | GTTTTGTTTTGTTTT[G/T]TTTTTGTTTTTTGAG | 286053 |
rs28469260 | snp | A/G | 0.162581 | 0.234218 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125175772 | GCAATAAAATGACAC[A/G]CTTTAAGTAATTACA | 286053 |
rs28481333 | snp | C/T | 0.0607341 | 0.163335 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257031 | GTCCGGGCCTGTAAT[C/T]GCAGCGCTTTGGGAA | 286053 |
rs28502126 | snp | A/C | 0.0748431 | 0.178382 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125328764 | CTGTCATCTGGGTCT[A/C]CACTTTCTGTTTTTT | 286053 |
rs28508203 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217370 | ATTTATTTTTTATTT[A/T]TTTATTTTGAGATGG | 286053 |
rs28516407 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125252487 | GCTGAGATCCCGCCA[C/T]TGCACTCCAGCCTGG | 286053 |
rs28535453 | snp | A/G | 0.0670745 | 0.170406 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125113940 | TTTTATGAATTTGAT[A/G]GGATTCTTCTCCCTT | 286053 |
rs28535909 | snp | C/T | 0.472803 | 0.113397 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316731 | TTCTTTCTTTCCTTC[C/T]TTTCCTTCCTTCCTT | 286053 |
rs28537981 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125233440 | AATATTTTATTTATG[G/T]AGGATTTTTATTCCT | 286053 |
rs28549168 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125265021 | ACTTAAGGGGATGCC[A/C]AAAACTCAGTAATCA | 286053 |
rs28551025 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125213657 | TCTCTCTTTCTCTGT[C/T]TCTCTCTCTTTCTCT | 286053 |
rs28552451 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125314293 | TTTTGTTTTGTTTTG[G/T]TTTTGTTTTTTGAGA | 286053 |
rs28597078 | snp | C/T | 0.162253 | 0.234095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218372 | AATATAAAAACTCCA[C/T]ATGCATTTGGGATAA | 286053 |
rs28609750 | snp | C/T | 0.11228 | 0.208646 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125233297 | AGAATTTTTAAAGCA[C/T]GGTAAATCAGAACCA | 286053 |
rs28654074 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125247688 | CGAGATTGCATCATT[A/G]TACTCCCACTGGACA | 286053 |
rs28679282 | snp | A/G | 0.106987 | 0.205054 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125342503 | AAAGTGGACAAGGAG[A/G]GGGTGGGTGAGAGGA | 286053 |
rs28700192 | snp | A/G | 0.162909 | 0.23434 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125178630 | AATCCCAGCACTTTG[A/G]GAGGTGGAGGCGGGC | 286053 |
rs28702877 | snp | C/T | 0.0551013 | 0.156571 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125253890 | CTACCACATATGCAG[C/T]TAAATGACAATTCCC | 286053 |
rs28723563 | snp | C/T | 0.499928 | 0.00598999 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316732 | TCTTTCTTTCCTTCT[C/T]TTCCTTCCTTCCTTC | 286053 |
rs28728068 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125213655 | TTTCTCTCTTTCTCT[G/T]TTTCTCTCTCTTTCT | 286053 |
rs28867439 | snp | A/G | 0.23031 | 0.249223 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125104543 | GGTCCTAGGTCCTAC[A/G]TGACTGAACCTGGGA | 286053 |
rs33934962 | in-del | -/AC | 0.161267 | 0.233723 | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125129354 | TGAAAGGATACTTAA[-/AC]ATCTTTTTAAGCCTA | 286053 |
rs34003830 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125343473 | GAAAACATATTATAT[-/A]AAATTTAAAGTATGA | 286053 |
rs34006623 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125246997 | CTATAGTCACGTTGC[-/T]TTTACTATGATTAAA | 286053 |
rs34058076 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125359944 | AAGGAGGCATGAGGC[-/A]AAAAAAAAGTCAGTT | 286053 |
rs34078935 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125205666 | TATTCTTTGTTTTTG[G/T]TACTCTTTGTTTACC | 286053 |
rs34095232 | in-del | -/T | 0.244776 | 0.249945 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125137084 | CAAAATTTTTTTTTT[-/T]ACTTTCCAACAATAA | 286053 |
rs34110249 | snp | A/G | 0.135825 | 0.222405 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125192217 | ATAATTATCTTGTTG[A/G]GTTATAATTCCTGAA | 286053 |
rs34130712 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125292221 | AGAAGCTATGGGAGG[-/A]AAAAAAAAAAAGGAG | 286053 |
rs34140290 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125254862 | CCTGAAAGAGCTCAT[-/G]GGGCACGTAAAGGAA | 286053 |
rs34143073 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125229250 | TGCAAGAGACTGGGA[-/G]GAAATAATCTAAGCA | 286053 |
rs34143139 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125344749 | TTCATCTCAAAAAAA[-/A]AAAAAAGAAAAGAAA | 286053 |
rs34148362 | in-del | -/TG | 0.375 | 0.216506 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125294381 | TAGGAACTGCCAGAC[-/TG]TTTTCCAAAAGGACT | 286053 |
rs34154199 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125149767 | TAGTTACAATAACTG[-/A]AAATATTTGTGGATC | 286053 |
rs34159520 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243404 | AAAGATGTTCCAAAA[-/G]GGAAGATCCAAAAGG | 286053 |
rs34179439 | in-del | -/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125182750 | GTGGTAGTATAAATT[-/C]CCATGTGGTTTTTAA | 286053 |
rs34189421 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125293604 | GTCATCAAGCATACT[-/G]GATGAGTAGAGGTAA | 286053 |
rs34193294 | in-del | -/A | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125284198 | AAACATTTAGAGAGT[-/A]AAAAAAAAAAAGAAA | 286053 |
rs34199531 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125177415 | CACTCTCATTCCCAT[-/G]GATCTGCTTCTCATC | 286053 |
rs34201191 | snp | C/T | 0.375 | 0.216506 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125330181 | TTTTCTTTTTTCTTT[C/T]TTTTTTTTTTTTTTT | 286053 |
rs34202558 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125143292 | AGATGTCTTCTTTAC[-/A]AAAATATAGAAAAAT | 286053 |
rs34213706 | in-del | -/TT | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125334799 | TTTTTTTTTTTTTTT[-/TT]GAGACACAGTCTCGC | 286053 |
rs34215353 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125178821 | TTGCAGTGAGCCGAG[-/T]ATCGTGCCACTACAG | 286053 |
rs34237629 | in-del | -/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218415 | CTGAAAAATTGAGGG[-/T]TTTTTTTTTTTTTTG | 286053 |
rs34246020 | snp | A/G | 0.135484 | 0.22223 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125234086 | TAGTCCCAGCTACTC[A/G]AGAGGCTGAAGCAGG | 286053 |
rs34262015 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125288566 | GTCCTTTTTCCTGGC[-/A]AAATCTCTGTACTTA | 286053 |
rs34272799 | in-del | -/C | | | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125129355 | GAAAGGATACTTAAA[-/C]ATCTTTTTAAGCCTA | 286053 |
rs34283161 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125150478 | TCACTCTGTTGCCCA[-/G]GCTGGAGTGCAATAG | 286053 |
rs34284298 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125134723 | TTTTTAACGGATTCC[-/T]TTTTTTTTTTTTTTT | 286053 |
rs34298715 | snp | G/T | 0.135484 | 0.22223 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125216131 | GCTTTAATGTTCACC[G/T]ATGTTGTAGCATGTA | 286053 |
rs34307563 | in-del | -/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125269532 | TTGATCAATTTATTT[-/C]CCTGTGCTCATCATG | 286053 |
rs34313605 | snp | A/G | 0.218151 | 0.247963 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125259706 | TTAACAGTAGTAATC[A/G]TAATATAAACAATAG | 286053 |
rs34313970 | snp | C/T | 0.202035 | 0.245356 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125176688 | CATCAGACAGGTGAG[C/T]GCTTTATTGCTTCAT | 286053 |
rs34330163 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125241718 | AGTGGTGATTTTAAC[-/A]AAAAGTACTCATAGT | 286053 |
rs34345598 | in-del | -/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125330177 | ACTTTTTCTTTTTTC[-/T]TTTTTTTTTTTTTTT | 286053 |
rs34357752 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125155192 | AAAATAAAGCATTCA[-/G]GGGAGAGTTAATAAC | 286053 |
rs34383419 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125361138 | CTCTGTCTCCCAGGC[-/T]TGGAGTACAACCTCT | 286053 |
rs34397318 | in-del | -/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196560 | GCTACATAGTATTCC[-/C]ATGGTGTATATGTGC | 286053 |
rs34415531 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125270905 | GACACCATCTCTTAG[-/T]AAAAAAGAAAAAAAA | 286053 |
rs34421417 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125359331 | TTCTTGCTCTTTCTC[-/T]TTTTTTTTTTTTTTT | 286053 |
rs34427316 | snp | A/T | 0.135825 | 0.222405 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125174185 | CAATAATCTGCTTGA[A/T]TATTTGAATATTTGT | 286053 |
rs34448805 | snp | A/G | 0.135825 | 0.222405 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125191332 | CCCATGTTCTTTCCC[A/G]CATACCACACCAATT | 286053 |
rs34461511 | snp | C/T | 0.136506 | 0.222754 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125143878 | AAGGTAAAGAAGTTT[C/T]GTAGACCCATAAGGT | 286053 |
rs34462465 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125169821 | TTTCTTTACATGGTG[-/T]ACACCCCTCCTTACC | 286053 |
rs34476126 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125205484 | TTCTGTATCTGCTGC[-/G]TTTTGGTGATGGTGC | 286053 |
rs34480342 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125350605 | TGGCAGAAGACAAGG[-/T]AAGAGCAAGTCACAT | 286053 |
rs34480931 | in-del | -/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125333160 | AAGAATCTAGATTTC[-/T]TTTTTTTTTTCTTTT | 286053 |
rs34490847 | in-del | -/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125350526 | AAAGACATACCTGAG[-/C]ACTGGCAAGAAAAAG | 286053 |
rs34507498 | snp | C/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196525 | TGTCCCTACAAAGGA[C/T]ATGAACTCATCATTT | 286053 |
rs34518383 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125108978 | AAGATCCAGTTTTAG[-/T]AAAGATAACTGTCCA | 286053 |
rs34532295 | snp | C/T | 0.201727 | 0.245295 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125141871 | TTTGAAACATTTTTC[C/T]CCTCTGCCTAACATG | 286053 |
rs34532572 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125332758 | CAAGAAGCTTGCTCA[-/G]GGGAGAGGTTCCTGC | 286053 |
rs34537234 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125239279 | ATATACCTTAGTGGA[-/T]TTTGAAACAACATCT | 286053 |
rs34556187 | snp | A/G | 0.0547245 | 0.156101 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125275765 | TGAATAAATACTAAT[A/G]TCCAGATTTTTTTTT | 286053 |
rs34556365 | in-del | -/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125265159 | ATTTAATTTTTTTTT[-/T]GGTAGTTCATGAATT | 286053 |
rs34565896 | in-del | -/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125254617 | AGATTTTTTTTTTTT[-/T]AATAAAGGACTATAA | 286053 |
rs34574004 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125236759 | CCCACTGATAGAAAA[-/A]GTACTCCCTCTACCA | 286053 |
rs34582058 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125235079 | GGTGAAAACCCACCT[C/T]TACTAAAAATACAAA | 286053 |
rs34588452 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125210306 | TACTACATCATGTAG[-/A]AATAGATAATTGCTT | 286053 |
rs34592007 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125273616 | CAGTTTATGGACATA[-/T]TTTGAGGTTGCAACT | 286053 |
rs34606312 | in-del | -/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272015 | TTTTTTTTTTTTTTT[-/T]GAGACGGAGTCTCGC | 286053 |
rs34646266 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125131607 | TGAGTTCTAACGTGG[-/A]AAAAAAAAATGCTTG | 286053 |
rs34647518 | snp | G/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125333503 | TAGTTTTCCTGGTGG[G/T]TCTTTTTTTTTTTTT | 286053 |
rs34656029 | in-del | -/T/TT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125096655 | TTTTTTTTTTTTTTT[-/T/TT]CATACGGAGTCTTTT | 286053 |
rs34659401 | snp | A/G | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196578 | CTGGATTAAGAAAGT[A/G]TGGCACATATATACT | 286053 |
rs34667555 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125328152 | GACTTCTCACTGGCC[-/T]TTTTTTTTTTTTTTT | 286053 |
rs34671072 | snp | C/G | | | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125129003 | AATCTCCTCACAGCA[C/G]ATAAGAACACGTTTT | 286053 |
rs34676045 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125099008 | GTTTTAGGTGCTGGA[A/G]ATACATAGTATTACA | 286053 |
rs34687223 | in-del | -/T | 0.5 | 0 | intron-variant, downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125195880 | TTTTTCCTGAATAAC[-/T]TTTTTTTTTTTTTTT | 286053 |
rs34694976 | snp | C/T | 0.141596 | 0.225274 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125106639 | GCAGTGAGCAGAGAT[C/T]AGGCCACTGCACTCC | 286053 |
rs34695377 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125292006 | TTCAAGCTGGTCCAT[-/G]GGGGAAAGAATGAGA | 286053 |
rs34712354 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125267877 | TTCAAAAAGTTTAAT[-/G]CTGGTGGAATTAGGA | 286053 |
rs34715537 | in-del | -/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125192329 | TTCATTTTTAAAAGG[-/T]TTTTTTTTTTTTTTT | 286053 |
rs34722934 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196747 | GGTCAAATGGTATTT[-/T]CTAGTTCTAGATCCC | 286053 |
rs34724865 | in-del | -/A | 0.471578 | 0.115772 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125161791 | AAAAAAAAAAAAAAA[-/A]TCGGAAACGGTAACC | 286053 |
rs34737949 | snp | A/G | 0.136847 | 0.222927 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125115722 | ACAGAGCGAGACTCC[A/G]TCTCAATAAAAAAAA | 286053 |
rs34744353 | in-del | -/C | 0.242775 | 0.249896 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125200577 | TCCCTTTGTGGGTAA[-/C]CTGACTTTTCTCTCT | 286053 |
rs34754080 | in-del | -/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125111156 | ACCTTAATCCCCACG[-/C]CAGCCAAAAAAGTTT | 286053 |
rs34757076 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125110062 | TTAGTAAGCGCTTTA[A/G]GTTTAGTTAAGTAAA | 286053 |
rs34763403 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125234012 | AACCCTGTCTCTACT[-/A]AAAAAAAAAAAAAAA | 286053 |
rs34777858 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125224148 | TCCTTTGCCCATTTT[-/A]AAAATCAGGTTATTT | 286053 |
rs34793900 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125155908 | CACAGGGAAAATGAT[-/G]GGGAATGTAGCTAAA | 286053 |
rs34800965 | in-del | -/AC | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125285768 | CACGCACACACACAC[-/AC]ACACACACACAAAGC | 286053 |
rs34820122 | in-del | -/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125261399 | TTATTATTTATTGAA[-/C]GCATCTGCTCTTTCT | 286053 |
rs34853232 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125147786 | TTCTGTGTTTATCCC[-/T]TTTTCCCCCTCCAAA | 286053 |
rs34880687 | in-del | -/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125219668 | TTTTTCTTGGGCTTT[-/C]CTGGAAAAGCTAGAT | 286053 |
rs34892282 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125325314 | ATAAAATAAAATAAA[A/G]TAAAATAAAATAAAA | 286053 |
rs34900855 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125113638 | AACACAATAAAGTGT[A/T]AACCAACCTTTCAAC | 286053 |
rs34903473 | snp | C/G | 0.137187 | 0.223099 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125144034 | TAAATGTGTGTGGAC[C/G]TGATAGGGAAAAGAG | 286053 |
rs34912537 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125205660 | GCGAGCTATTCTTTG[G/T]TTTTGTTACTCTTTG | 286053 |
rs34931746 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125223312 | GCTATGAGTCAAGAT[G/T]GCACCACTGCACTCC | 286053 |
rs34940610 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125155897 | ACCTTAATTCTCACA[-/G]GGGAAAATGATGGGA | 286053 |
rs34955184 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196542 | ATACTATGCAGCCAT[-/A]AAAAAGGATGAGTTC | 286053 |
rs34996950 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125364639 | GCATGCCTGTGTGGG[-/T]ATATATGCAAGATAG | 286053 |
rs35012831 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125264146 | CCTAGAGTAAGCCCT[-/A]AAAGCAGTAGATGTG | 286053 |
rs35014556 | in-del | -/AG | 0.385359 | 0.210185 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125142792 | ATTTTTAGTAGAGAC[-/AG]GGTTTCTCCATGTTG | 286053 |
rs35031300 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125318308 | TAGTAGGGCTGAGGT[-/G]GGGAAGATCACTTGA | 286053 |
rs35033076 | snp | C/G | 0.135484 | 0.22223 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218962 | CTCCATTTGGTCTCT[C/G]CAGACCAAATTTTCT | 286053 |
rs35048026 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125343531 | TAGTCCCAGCTACTC[-/G]GGGGAGCTGAGGTAG | 286053 |
rs35070018 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125341886 | GCAATGCACTGAGGA[-/T]TCTAGAAATGGAAAA | 286053 |
rs35090041 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125223309 | GTTGCTATGAGTCAA[A/G]ATTGCACCACTGCAC | 286053 |
rs35093256 | in-del | -/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125240964 | CAAAATTAGCAGCTT[-/C]CCATGGTCACTGGTG | 286053 |
rs35094108 | in-del | -/G | | | intron-variant, utr-variant-5-prime | NSMCE2 | GRCh38.p7 | 8:125129984 | AAATAGTAAGCTCCA[-/G]GACTTTATTTGGATT | 286053 |
rs35114839 | snp | A/C | 0.384785 | 0.210554 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125222507 | TTGGCCAACATCTCC[A/C]CATTTTCCCAACCCC | 286053 |
rs35118249 | in-del | -/G | 0.170084 | 0.236883 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125259204 | TACTCACAGAGCTTT[-/G]TAAAGAGAAAGTGAG | 286053 |
rs35120930 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243884 | CTTCAAAGAGCAACA[-/G]GGAAGATCATCTTTG | 286053 |
rs35135540 | in-del | -/A | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125297834 | GTCTCAAAAAAAAAA[-/A]TTATTGATTACTTTT | 286053 |
rs35140299 | snp | C/T | 0.145305 | 0.227022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125134715 | CCTCTTTGTTTTTAA[C/T]GGATTCCTTTTTTTT | 286053 |
rs35169174 | in-del | -/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125231491 | ATGCCTGTCTTTGTT[-/C]CCCTGGAACAGAGTT | 286053 |
rs35175471 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125206219 | GACTTGAGGAACAGC[-/A]AAATAAAATAATCCA | 286053 |
rs35178048 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125269382 | GAGCCACTGCACCCA[-/A]GCCGACTCTTTAACT | 286053 |
rs35188268 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125106406 | ACTTTGGGCTGAGTG[-/G]TGGTGGCTCATGTCT | 286053 |
rs35192094 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125328151 | GACTTCTCACTGGCC[-/T]TTTTTTTTTTTTTTT | 286053 |
rs35201440 | snp | A/C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125241367 | TAGGCAATCAAATAT[A/C/G]CAATTATAATACAGA | 286053 |
rs35212928 | in-del | -/A | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125304960 | AAGGAAGGAAGGAAG[-/A]AAGAAAGAAAAAGGA | 286053 |
rs35215140 | snp | C/T | 0.139564 | 0.224285 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125188746 | GCTTTCAGGATACTG[C/T]GAACTAAGGCCAAAA | 286053 |
rs35227530 | snp | C/G/T | 0.375 | 0.216506 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196734 | TAATGGGATGGCTGG[C/G/T]TCAAATGGTATTTCT | 286053 |
rs35232287 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125158090 | TTCAGAACCCACTTT[-/G]GGGAAGTGCTGCTGT | 286053 |
rs35232344 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125276299 | AATCTGTTTCCCACT[-/G]CTGATTTGCTTCCAA | 286053 |
rs35241769 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125114711 | AAAGAACTGTGCAGC[C/T]TAAGCTGTCATTAGT | 286053 |
rs35265954 | snp | G/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125299963 | AGTTGGGACTACAGG[G/T]GCACGCCATCATGCT | 286053 |
rs35277784 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125108587 | TGTTGGGACTAATGA[-/G]GATAATATATGCTAA | 286053 |
rs35280387 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125265510 | CAAGCATGAGCCACT[-/G]GCACCTAGTCTTTTG | 286053 |
rs35286873 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125122661 | TCTCCCACCCAAACC[-/A]AAATTGATCTCTTCT | 286053 |
rs35287869 | in-del | -/G | 0.135484 | 0.22223 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125232848 | GTACTAAAAAAGATA[-/G]GTTGGTAGTTGAGAC | 286053 |
rs35290472 | in-del | -/T/TT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218414 | CTGAAAAATTGAGGG[-/T/TT]TTTTTTTTTTTTTTT | 286053 |
rs35294120 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125174691 | CACAATTTTTCCGAA[-/A]GGCTCGAAGGAGGAA | 286053 |
rs35299244 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125335838 | CATTGCTCAACCAAA[-/G]GGGGAAAGTTCAAAG | 286053 |
rs35309384 | snp | A/G | 0.194902 | 0.243853 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316532 | CAACCAGCAGGTCTT[A/G]GAATAACCGTTGTCT | 286053 |
rs35333171 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125266700 | TCCAGTATACCTGTT[-/G]GGGGATGAATAGCAA | 286053 |
rs35334691 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298688 | AAATTCATCTGTGGG[-/T]TTTTTTTTTTTTTTT | 286053 |
rs35336507 | snp | A/G | 0.214541 | 0.247473 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243776 | TGTATCCAATTACCT[A/G]ATAGTCCCGCATGCT | 286053 |
rs35368452 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125137411 | GACCCTATTCGTATC[-/T]TTTTCTTGGTATAAA | 286053 |
rs35380657 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125160479 | TGGCTTGGGGTATGG[-/A]AAGTTAGTGCTCATA | 286053 |
rs35401436 | snp | A/T | 0.139225 | 0.224118 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125173034 | CAAACCAACAGGTGT[A/T]CCAGGTTCCAGACAC | 286053 |
rs35416238 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125220963 | GGCCCTGTGGGTGCT[-/A]AAAATATCTCGAAGG | 286053 |
rs35416397 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125106113 | TAACAAAGTAGTCAA[C/T]ATAAACTAACCAAGT | 286053 |
rs35421395 | in-del | -/CC | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125312189 | TAATAAACTTTGATG[-/CC]TCTCTGTTCTATGCT | 286053 |
rs35423372 | in-del | -/A/AA | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125312093 | AAAAAAAAAAAAAAA[-/A/AA]GAAAGAAAAGAAAAG | 286053 |
rs35429077 | in-del | -/AC | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125349011 | GGATCTCAAAGCAAA[-/AC]ACACACACACACACA | 286053 |
rs35441944 | in-del | -/T | 0.0379877 | 0.132479 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125175125 | AACAACTTTACCAAG[-/T]TTTTTTTTTGCTATA | 286053 |
rs35443773 | in-del | -/A | 0.460925 | 0.134204 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125271260 | AAAAAAAAAAAAAAA[-/A]GTATTACTCTAGTGA | 286053 |
rs35448180 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125183819 | AAACTCTGATTGGCA[-/G]GCTTTCGATTTCTTG | 286053 |
rs35463931 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125331588 | GATCTTTTTTTTTTT[-/T]AACAAAATAACCAGA | 286053 |
rs35475899 | snp | A/G | 0.135825 | 0.222405 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125174833 | CTTAAGTGTTTTGTC[A/G]AAAGTCAAAACCATG | 286053 |
rs35485568 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125204832 | TGCTCTACTTCTGAT[-/A]CTTGCTGTCAGCCTC | 286053 |
rs35494894 | in-del | -/AA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125247724 | GCAAAATTCTGTCTC[-/AA]AAAAAAAAAAAAAAA | 286053 |
rs35498012 | in-del | -/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125346336 | GGAGACAGACTCAAG[-/C]ATAAAGATGGAGAAT | 286053 |
rs35522991 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125094788 | GATGGCTGCCCTTTT[-/T]ATGTGTCTTCACATG | 286053 |
rs35539255 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125293163 | ATTCTGGGTACCATT[-/A]CTAAGAATGCTATTA | 286053 |
rs35563409 | snp | A/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196658 | ATAGTGCTGTAATAA[A/T]CAGACGTGTGCATGT | 286053 |
rs35564243 | snp | A/G | 0.136166 | 0.22258 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125159327 | TTCAGTTAACGAGGG[A/G]CCATACATATGATGG | 286053 |
rs35584303 | in-del | -/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125290791 | GTTAGACAGACAACT[-/C]CCTACCACCACCAAA | 286053 |
rs35604388 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196740 | GATCACTGAGTCAAA[C/T]GGTATTTCTAGTTCT | 286053 |
rs35636109 | in-del | -/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125116905 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGCCTCTC | 286053 |
rs35656783 | in-del | -/A | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125216635 | GCGAGGCTGTGTGTC[-/A]AAAAAAAAAAAAAAA | 286053 |
rs35658538 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125337885 | GCGAAACTCTATCTC[-/A]AAAAAAAAAAAAAAA | 286053 |
rs35658963 | in-del | -/T | 0.201727 | 0.245295 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125230704 | TTAATGGATAAAAGG[-/T]ACAAAGAAATTACCA | 286053 |
rs35674231 | in-del | -/TA | 0.387074 | 0.209071 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125236366 | GACGAGTTGCAAAAC[-/TA]TATATATATATATCA | 286053 |
rs35721214 | in-del | -/G | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125091917 | GGGTCTAGGCAGGGG[-/G]AAATTGGGGTGCCAC | 286053 |
rs35735576 | in-del | -/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125355182 | AAACACCTCATCTGG[-/C]CTAGGTGATGGCCCA | 286053 |
rs35737173 | in-del | -/CT | 0.0722614 | 0.17581 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125361375 | ACCTGACCACAGTCA[-/CT]TTTTTGCTTTTTTGT | 286053 |
rs35741998 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125276528 | AATAATTAATAATGG[-/A]AATAGCCTCATTTGA | 286053 |
rs35747622 | in-del | -/A | 0.248755 | 0.249997 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125112560 | ATATTATTCAGTCTT[-/A]AAAAAAAAATGAAAT | 286053 |
rs35755944 | in-del | -/TTTAT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316635 | TCCTTCTTTCCTTTC[-/TTTAT]TTCCTTCTTTCCTTC | 286053 |
rs35757565 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125313489 | ATCTCAACCAGCTGT[-/G]AAGCTCCAAATTTGT | 286053 |
rs35763247 | in-del | -/C | | | intron-variant, utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125363098 | CATCCCAGCAACCTA[-/C]CTTGGAGTTGCATTT | 286053 |
rs35774093 | snp | C/T | 0.136166 | 0.22258 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125159403 | GTGTTTACATATGTT[C/T]AGATACATAAATAGT | 286053 |
rs35779726 | snp | C/G | 0.385359 | 0.210185 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125142657 | TTGCCCATGCTGGAG[C/G]ACAGTGGTGCTATCT | 286053 |
rs35798929 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125205481 | ATGTTCTGTATCTGC[-/G]TGCTTTTGGTGATGG | 286053 |
rs35799588 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125170145 | TCAGACATATAACTG[G/T]CTTCTCTTCATTTTC | 286053 |
rs35812428 | in-del | -/A | 0.13446 | 0.221699 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125180808 | ATAATGGCAGCTAAT[-/A]AATTGTGGCTTTTAG | 286053 |
rs35820922 | in-del | -/AT/TA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272700 | ATATATATATATATA[-/AT/TA]ATATATATATATACA | 286053 |
rs35822368 | snp | G/T | 0.134119 | 0.221521 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125176914 | TGGCCTGCACTTATT[G/T]TGAGTTTCCTCATAT | 286053 |
rs35823474 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125359266 | TGATACTCTGTCTCC[-/A]AAAAAAAAAAAAAAA | 286053 |
rs35831885 | in-del | -/A | 0.428333 | 0.175206 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125250334 | AATGTTTTTCTTTTT[-/A]AAAAAAAAGCATCCT | 286053 |
rs35851817 | in-del | -/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125269987 | ACGGCCCTTATGGTT[-/C]CTTTAGGACTAGTCT | 286053 |
rs35851979 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125328852 | TAATATCCAAGGTCA[-/T]TTAGTCCCAACCCTC | 286053 |
rs35853383 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125227772 | ATCACCTGTAATCCC[-/G]GTTACCCAGAGATAA | 286053 |
rs35856259 | in-del | -/A | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125232364 | TCTCAAAAAAAAAAA[-/A]GAAAGAAAGAAAGTA | 286053 |
rs35856756 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125303475 | TAAAATAAAAGGTCA[-/G]GGGGTATCCATTTTT | 286053 |
rs35861494 | snp | A/G | 0.123105 | 0.215401 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125120866 | TGAATTTCTTTGAAG[A/G]CCTTGTAGAATCAGA | 286053 |
rs35878426 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125172289 | ATTCTTGCTGCAGGG[-/G]AAAGCTGAGAGAATT | 286053 |
rs35885162 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125190907 | GGAGTTTCGCTCTTA[-/T]TTGCCCAGGTTGGAG | 286053 |
rs35885401 | in-del | -/GT | 0 | 0 | intron-variant, upstream-variant-2KB | NSMCE2 | GRCh38.p7 | 8:125129578 | TGTGTGTGTGTGTGT[-/GT]CTGTGTGTTTCATTG | 286053 |
rs35904308 | in-del | -/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125103650 | CCCATAAATCAGTGG[-/C]AACTTGATAGATTTT | 286053 |
rs35904726 | in-del | -/G | | | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125093313 | ATACCATCACCTTGG[-/G]AAGTTAGGATTTCAA | 286053 |
rs35905480 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125126342 | CGCCATAGCACTCCA[-/G]CCTGGGTGACAGTGT | 286053 |
rs35920695 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125322735 | CAAAAAAGCTGCTAG[-/A]ACTAATACGTGAGTT | 286053 |
rs35925091 | in-del | -/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125253435 | GGTGTTTGGGGAATT[-/C]CCTGCAATATACCTT | 286053 |
rs35955519 | snp | G/T | 0.214239 | 0.247429 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243785 | TTACCTAATAGTCCC[G/T]CATGCTAAAAATAAT | 286053 |
rs35958010 | in-del | -/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125328906 | ACTGTTTCAGTGAGA[-/C]CCCGAAGTCAGAACT | 286053 |
rs35962231 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125099669 | CAAATTTAACATTAA[-/A]GTCTTTTCAGGTGAC | 286053 |
rs35985286 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125246975 | GTATACTATATAATA[-/T]TTGTTAACTATAGTC | 286053 |
rs35990794 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125267004 | TTTCTTTTTTCTTTC[-/T]TTTTTTTTTTTTTTT | 286053 |
rs35991395 | snp | C/T | 0.135484 | 0.22223 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125227230 | GGAGCAGGCCTGCCA[C/T]GTCCCTGACATGGCA | 286053 |
rs35997683 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125221936 | GTCTTCACACAGGGC[C/T]TAGCATAAAGTAGAC | 286053 |
rs36004071 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125229423 | CTCCTTTCCAGTGGA[-/T]TTTTCTTGTGACCCA | 286053 |
rs36020150 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125356327 | CTTTTAATTTTTTGG[-/T]TTTTTTTTTTTTTTT | 286053 |
rs36029936 | snp | A/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125246943 | TCAGCATTCTTAAGT[A/T]TTTCAAACCAATCTC | 286053 |
rs36036418 | in-del | -/A | 0.451234 | 0.14834 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243502 | AAATAATAATTTTTT[-/A]AAAAAAAAAACCTCT | 286053 |
rs36038487 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125178210 | TTCTCGCTGCCTGTT[-/G]GGGTCAGGTCTCAGT | 286053 |
rs36041361 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196558 | ACATATACACCATGG[-/G]AATACTATGCAGCCA | 286053 |
rs36042515 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125172349 | CTAAAGTGAGAAATT[-/A]CCCAGATTTAGGATA | 286053 |
rs36046999 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125288327 | GATAATTTTTTTCTT[-/G]CTGATATCAGCTCTT | 286053 |
rs36067888 | in-del | -/C | 0.498437 | 0.0279115 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125261531 | TGGAGATTCAGCACA[-/C]TTCAGGCATTTTAAT | 286053 |
rs36076702 | in-del | -/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125120141 | TCTTACAGTACATGT[-/C]CAACCTGGACTAGCC | 286053 |
rs36081564 | snp | A/T | 0.218151 | 0.247963 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125161303 | TGGACTTCCTTTTTT[A/T]AAAAAAAAGTCTAAT | 286053 |
rs36097485 | in-del | -/AC/CA | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272847 | ATATACACACACACA[-/AC/CA]TATATATACACACGT | 286053 |
rs36124251 | snp | A/C | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125223092 | TAAAATAAAATAAGC[A/C]CGGTGGCTCACACCT | 286053 |
rs36192929 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125274929 | GGGAGACTCAGTCTC[-/A]AAAAAAAAAAAAAAA | 286053 |
rs36196138 | in-del | -/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196700 | AGCATGATTTATAAT[-/C]CTTTGGGTATATACC | 286053 |
rs55740518 | snp | A/T | 0.188 | 0.24219 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125158188 | TGTGGCATCCAGAAA[A/T]CTGGGAAGTATGTCG | 286053 |
rs55759755 | snp | C/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316655 | TTCCTTCTTTCCTTC[C/T]TTCCTTCCTTCCTTC | 286053 |
rs55760846 | snp | A/C | 0.297636 | 0.24542 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125227567 | TAATTACATCATCTT[A/C]ATTGCAAATGTATTG | 286053 |
rs55792228 | snp | C/T | 0.281313 | 0.248031 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125285755 | AATTCTTCATACACA[C/T]GCACACACACACACA | 286053 |
rs55804496 | snp | C/T | 0.375 | 0.216506 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272858 | ATATACACACACACA[C/T]ATATATACACACGTA | 286053 |
rs55808247 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125320237 | GGGAGGGAGGGAAGG[A/G]AGGGAGGGAGGGAGG | 286053 |
rs55808842 | snp | A/C | 0.195837 | 0.244062 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125325993 | CCGGGCGCGGTGGCT[A/C]ATGCCTGTAATCCCA | 286053 |
rs55823859 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125148910 | ATCCATTACATTAGG[A/T]TGTAAGTTGTTTAAA | 286053 |
rs55839055 | snp | A/G | 0.243061 | 0.249904 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125135272 | CCCAGGTTGGTCTCA[A/G]ATTCCTGGCCTTAGG | 286053 |
rs55843815 | snp | A/G | 0.0930568 | 0.194599 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125233102 | GCAGATCACTTTGAA[A/G]CTTGCCCAGTTTTTG | 286053 |
rs55927076 | snp | A/G | 0.232651 | 0.249397 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125266209 | AGATTCTCCTGCCTC[A/G]GCCTCCCGAGTAGTT | 286053 |
rs55940827 | in-del | -/AA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125337905 | AAAAAAAAAAAAAAA[-/AA]GAAAGAAAGAAAACA | 286053 |
rs55990581 | in-del | -/AAAAAAA | | | downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125367541 | AAAAAAAAAAAAAAA[-/AAAAAAA]GAATGTCTTTCAAGT | 286053 |
rs55992026 | snp | A/G | 0.175897 | 0.238765 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125100106 | AACTGATGCTGATAG[A/G]TGGAGAGGTAAGCGG | 286053 |
rs56079107 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125261835 | GGCACAGTGGCTCAC[A/G]TCTGTAATCCCAGCA | 286053 |
rs56084080 | in-del | -/GTAAAATAAA | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125325324 | ATAAAATAAAATAAA[-/GTAAAATAAA]ATAAAATGTGTATTG | 286053 |
rs56091727 | in-del | -/ATTTCCTTCCTTCCTTCCTT/ATTTCCTTCCTTCCTTCCTTATTTCCTTCCTTCCTTCCTT | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125213743 | CTTCCTTCCTTCCTT[lengthTooLong]CCTTCAACTGTACAG | 286053 |
rs56117234 | snp | A/G | 0.0633504 | 0.166319 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125345139 | GAATCAGAGGTGATC[A/G]GGGGCGTAGATGGTT | 286053 |
rs56131608 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316699 | TATCTTCCTTCTTTC[C/T]TTCCTTCCTTCTTTC | 286053 |
rs56135036 | snp | C/T | 0.133435 | 0.221162 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125207634 | CAAACCACCCCAAAA[C/T]GTAGTAGCTTAAAAT | 286053 |
rs56157039 | snp | A/G | 0.0792508 | 0.182605 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125285138 | AAATAACCTAAAACT[A/G]AAATGGCACAGTTTG | 286053 |
rs56201104 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125154529 | AAAAAAAAAAAAAAA[-/A]GGACTCATTCCAGCT | 286053 |
rs56225128 | snp | C/G | 0.165527 | 0.235296 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125242107 | GTAAACAATAACTGG[C/G]GGGGGAGTTTGAGAA | 286053 |
rs56253114 | in-del | -/TAT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125215056 | ATTTATTATTATTAT[-/TAT]ACTTTAAGTTTTAGG | 286053 |
rs56259065 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316683 | TTCTTTCCTTCCTTC[C/T]TATCTTCCTTCTTTC | 286053 |
rs56276829 | snp | C/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125193019 | TTAATATATTAACAA[C/T]GTATAATAGTTGAAG | 286053 |
rs56311879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125117954 | ATAAGCCCTTTTGTT[A/G]ATTTTTGAACCTAAT | 286053 |
rs56326134 | snp | A/C | 0.302435 | 0.244439 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125134974 | GTGCAGTGGCTCAAT[A/C]TTGGCTTATTGCAAA | 286053 |
rs56380777 | snp | C/T | 0.0810805 | 0.184299 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125209670 | CCTTTATGAATGAAT[C/T]CCTTTATCTAGTTTA | 286053 |
rs56393723 | snp | C/T | | | downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125367508 | CGACAGAGCAAGCCT[C/T]TAAAAAAAAAAAAAA | 286053 |
rs56397455 | snp | C/T | 0.0807149 | 0.183963 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125228532 | ACTTCCTGGAAGAGC[C/T]GACATTTGAGCTGAG | 286053 |
rs56704513 | in-del | -/CA | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125143122 | ACACACACACACACA[-/CA]GAGGTAGGTGCATGT | 286053 |
rs56704677 | snp | C/T | 0.0685596 | 0.171987 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125333290 | TCCTCCCCATTCAGC[C/T]TCCCAAGTAGCTGGG | 286053 |
rs56798105 | snp | G/T | 0.0209421 | 0.100162 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125102604 | ACCCCTCTAGGCATC[G/T]GTTGTCTCATTTTAT | 286053 |
rs56906621 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125312093 | AAAAAAAAAAAAAAA[-/A]GAAAGAAAAGAAAAG | 286053 |
rs56920013 | snp | C/T | 0.235854 | 0.249599 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125262937 | CTCCGCGAAAAAAGG[C/T]TGAAGATGAGTATCT | 286053 |
rs56972472 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125298712 | TTTTTTTTTTTTTTT[-/T]CCCCAGTTTAGGTCT | 286053 |
rs56988673 | snp | A/T | 0.0637235 | 0.166737 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125198256 | AGAGAGGGCAGCCTT[A/T]TCTTGTGCCGGTTTT | 286053 |
rs57062304 | snp | G/T | 0.111928 | 0.208413 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125220603 | TGAAAGTAATAAAAT[G/T]ACTCTTTCAGAAGGA | 286053 |
rs57148341 | in-del | -/CAGGG | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125161727 | CTTGAACCCAGGAGG[-/CAGGG]GTTGCAGTGAGCCAA | 286053 |
rs57252921 | snp | C/T | 0.243633 | 0.249919 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125125070 | AAAGTGCTGGGACTA[C/T]GGGTGTGAGCCCAGC | 286053 |
rs57337793 | in-del | -/A | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125337905 | AAAAAAAAAAAAAAA[-/A]GAAAGAAAGAAAACA | 286053 |
rs57421278 | in-del | -/T | 0.233235 | 0.249437 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125103831 | AGAATCTTTTTTTTT[-/T]AGTCTTCCATTTCTT | 286053 |
rs57511664 | snp | A/C/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125095292 | AATCAAGACTGAGTA[A/C/G]AAAACAGAATACTTC | 286053 |
rs57536119 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125220973 | GTGCTAAAAATATCT[C/T]GAAGGTATTTTTTAT | 286053 |
rs57559309 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125286330 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTCGC | 286053 |
rs57641068 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125210271 | AAATGTTATGTGTTA[A/G]CTATTCATTACTGTC | 286053 |
rs57687393 | snp | A/G | 0.0520825 | 0.152737 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125302528 | TTAGAGGTTAATATG[A/G]GGTGAGAATTGAGAG | 286053 |
rs57773151 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125170510 | CTCCCGGGTTCAGGA[A/G]ATTCTCCTGCCTCAG | 286053 |
rs57876250 | snp | A/T | 0.0588605 | 0.161139 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125135656 | TCCTAGCACCATTTG[A/T]TGCTGAAGACTGTTT | 286053 |
rs57905807 | snp | A/C | 0.237303 | 0.249677 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125201649 | GGCTACACAGCGCTC[A/C]GGGACCCACTTGAGG | 286053 |
rs57968397 | in-del | -/AAG | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125320258 | GGGAGGGAGGGAAGG[-/AAG]GAAGGAAGGAAGGAA | 286053 |
rs58179901 | snp | A/G | 0.236724 | 0.249647 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125190812 | TAATGAATAACAGCC[A/G]ACATTGTTTGAGTGC | 286053 |
rs58217279 | snp | C/T | 0.0204825 | 0.0991047 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125151315 | TTATATATTTGGTTA[C/T]AACTCACTGACCGAG | 286053 |
rs58241047 | in-del | -/C | 0.13446 | 0.221699 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125139704 | GTCTTTCACATGATA[-/C]ATGGGAATTGTGGGA | 286053 |
rs58318216 | snp | A/G | 0.144632 | 0.226711 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125337708 | GAGACCAGCCTGACC[A/G]ACATGGAGAAACCCC | 286053 |
rs58383711 | snp | A/G | 0.243347 | 0.249911 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125216413 | GGAAGGCCGAGGCAG[A/G]CAGATTACCTGAGGT | 286053 |
rs58458829 | in-del | -/GAAA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125313247 | AAAGAAAGAAAGAAA[-/GAAA]AGAAAAGAAGGAAAG | 286053 |
rs58493916 | in-del | -/CC/TTCCTTCC | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316732 | CTTTCTTTCCTTCTT[-/CC/TTCCTTCC]TTCCTTCCTTCCTTC | 286053 |
rs58527250 | snp | A/G | 0.114387 | 0.210022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125264279 | GTTTGTACTTCATTC[A/G]TATTCCTTTAAAAAG | 286053 |
rs58585963 | snp | A/G | 0.0752113 | 0.178743 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125309151 | ACTCAGGAGGCTGAG[A/G]CAGGAGAGAATCGCT | 286053 |
rs58600417 | snp | C/T | 0.0850919 | 0.187897 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125326818 | AAAATTAGCCGGTCG[C/T]GGTGGCGGGCACTTG | 286053 |
rs58650877 | snp | C/T | 0.197703 | 0.244469 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125349621 | AAAGAAAAGAAATGT[C/T]CCAGCCTAATTGAAA | 286053 |
rs58741237 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125256634 | TGTTCAGTTAAAAAA[-/A]GAAGAGGACTGTTGG | 286053 |
rs58789139 | in-del | -/TTT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125299829 | TTTTTTTTTTTTTTT[-/TTT]GTCTTGAGACAGAGT | 286053 |
rs58805022 | snp | A/G | 0.302686 | 0.244385 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125126853 | CTCACTTTATTTAGG[A/G]TTGATGTGAGAATTA | 286053 |
rs58843869 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125262922 | TGACCATTTCAGTGC[C/T]TCCGCGAAAAAAGGT | 286053 |
rs58851842 | in-del | -/TTG | 0.297382 | 0.245469 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125227569 | ATTACATCATCTTAA[-/TTG]CAAATGTATTGCAAT | 286053 |
rs59016298 | in-del | -/AAGA | | | intron-variant, downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125363542 | AGAAAGAAAGAAAGA[-/AAGA]GAGAGAGAGAGAGAG | 286053 |
rs59056247 | snp | A/G | 0.236434 | 0.249632 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125172269 | GGACTGAGGTGGCAT[A/G]TCTGTATTCTTGCTG | 286053 |
rs59062889 | in-del | -/A | 0.0376037 | 0.131863 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125235580 | GATACATGGAGTTAT[-/A]TTTTATACACATATA | 286053 |
rs59099103 | snp | A/C | 0.123452 | 0.215605 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125264514 | TGGGTTGAAACAATT[A/C]TCATTCCTCGGCCTC | 286053 |
rs59153330 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125234073 | TGTCAGGCGCCTGTA[A/G]TCCCAGCTACTCGAG | 286053 |
rs59169573 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125203865 | TTTTAAAAAATAAAA[-/A]TATAACTTGTTAGCT | 286053 |
rs59172051 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125257524 | AAACCAAATTTCTCT[C/T]TTTTTTTTTTTTTTT | 286053 |
rs59249754 | snp | A/G/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125238234 | ATGCAAGTAGAGCAG[A/G/T]CAGGGAACGAGGTTA | 286053 |
rs59285361 | in-del | -/GT/GTGT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125183662 | TGTGTGTGTGTGTGT[-/GT/GTGT]ATAGTATCTGGCACA | 286053 |
rs59357489 | in-del | -/AAG | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125320262 | GGGAGGGAAGGAAGG[-/AAG]GAAGGAAGGAAGGAA | 286053 |
rs59423445 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125134743 | TTTTTTTTTTTTTTT[-/T]AAGAGTCGGGGTCTT | 286053 |
rs59513985 | snp | C/T | 0.0618563 | 0.164627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125112136 | TGCTTATACAGCTTT[C/T]ATAACTGGAGCCAAC | 286053 |
rs59574355 | in-del | -/AA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125327285 | AAAAAAAAAAAAAAA[-/AA]GAGAGAGAAACCAAA | 286053 |
rs59630162 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125290804 | ACTCCTACCACCACC[-/A]AAAACCCAAGGAAGC | 286053 |
rs59667546 | snp | A/G | 0.0633504 | 0.166319 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243669 | TAAGGAATTATAAGA[A/G]CTATAAAGAACTATA | 286053 |
rs59684072 | in-del | -/T | | | intron-variant, downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125196218 | TTTTTTTTTTTTTTT[-/T]ATACTTTAAGTTCTA | 286053 |
rs59804104 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125192697 | AGCATTAATGTGGTA[A/T]CACAAAAAGGGCACA | 286053 |
rs59807496 | in-del | -/TATTAT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125215053 | TTTATTTATTATTAT[-/TATTAT]ACTTTAAGTTTTAGG | 286053 |
rs60051203 | snp | C/G | 0.145305 | 0.227022 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125331569 | ATAGATTTTCTCCTC[C/G]CTGAAGTTTAAAAAC | 286053 |
rs60052877 | snp | C/T | 0.0603597 | 0.1629 | downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125367387 | AGGTGTGGTGGTGCG[C/T]ACCTGTAATCCTAGC | 286053 |
rs60084058 | in-del | -/GT | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125294382 | AGGAACTGCCAGACT[-/GT]TTTCCAAAAGGACTG | 286053 |
rs60127810 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125324986 | GATAGGGATTACTAA[G/T]GGCACAAGGCAACTT | 286053 |
rs60153673 | in-del | -/G | 0.482459 | 0.0919928 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125113058 | ATATTAACAGAAAAT[-/G]GGGGGGGGGGTGAGT | 286053 |
rs60187894 | snp | G/T | 0.0528381 | 0.153711 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125142922 | TTCAGTTTTAATTTT[G/T]CCACACTAATATCTA | 286053 |
rs60203756 | in-del | -/AGGGAGGGAGGGA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125320234 | GGAGGGAGGGAGGGA[-/AGGGAGGGAGGGA]GGGAGGGAAGGAAGG | 286053 |
rs60256707 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125185315 | TTAAATTTTTTTTTT[-/T]CTTTTTTTTGAGACA | 286053 |
rs60308659 | in-del | -/A | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125256959 | AAAAAAAAAAAAAAA[-/A]AAAGAGAGTGAGGGG | 286053 |
rs60324416 | snp | A/T | 0.257732 | 0.24988 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125286315 | CAATACCTTTTATTT[A/T]TTTTTTTTTTTTTTT | 286053 |
rs60368750 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125347752 | AAGGAGATTGGCTAT[A/G]GAGATTGTGTTGGGT | 286053 |
rs60376711 | in-del | -/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125320310 | AGGAAGGAAGGAAGG[-/G]AAGGGAAGGAAGGGA | 286053 |
rs60388854 | snp | C/T | 0.0637235 | 0.166737 | intron-variant, upstream-variant-2KB | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125090156 | TACTAGACCTCCTAA[C/T]CCGGACTAGTTATAT | 286053 |
rs60425833 | in-del | -/CACA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125349060 | ACACACACACACACA[-/CACA]GAGCTCTTAATTCCA | 286053 |
rs60442484 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125235251 | TCTCAATTAAAAAAA[-/A]AAAAAAAGGAAACCT | 286053 |
rs60474927 | snp | C/T | 0.084728 | 0.187577 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125183118 | ACCTTCATTTACACA[C/T]ACATGGAGCAGGAGT | 286053 |
rs60494467 | snp | C/G | 0.264084 | 0.249603 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125096588 | TTTTGTTTTGATTGT[C/G]AGGAAGCTCACTACC | 286053 |
rs60501763 | in-del | -/TGGGGGCGTAGATGGTTTCTGGCCAGGGAACAGAATCAGAGGTGAT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125345183 | AGAATCAGAGGTGAT[lengthTooLong]CTAAATACGTATGTG | 286053 |
rs60524861 | snp | A/C | 0.0240643 | 0.107019 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125112155 | ACTGGAGCCAACTAT[A/C]CCAGCAAAATAGCAT | 286053 |
rs60707679 | in-del | -/A | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125216650 | AAAAAAAAAAAAAAA[-/A]TGGTCTATGGGTTTT | 286053 |
rs60712783 | snp | C/G | 0.0329836 | 0.124112 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125329983 | CCCCTCCGAAAGAAC[C/G]ATCATTACCTAGAAT | 286053 |
rs60732204 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125277523 | TTCTTTTTTTTTTTT[-/T]CGAGATGAAGTCTCG | 286053 |
rs60790549 | in-del | -/CA | 0.00597247 | 0.0543191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125243915 | TCACTGAAAGACTCA[-/CA]ACATATCCCACTTCT | 286053 |
rs60829601 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125329528 | TTTAGTTGGAATCCA[C/G]GTCTGCCTTTAGTTA | 286053 |
rs60878859 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316707 | TTCTTTCCTTCCTTC[C/T]TTCTTTCCTTCTTTC | 286053 |
rs61005010 | snp | A/C | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125354219 | TTACAGGCGTGAGCC[A/C]CCGCACCCAACCTTG | 286053 |
rs61055867 | snp | C/T | 0.0685596 | 0.171987 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125350154 | TTTCCTGGAAGAGAA[C/T]GAGGGAGGGGGAGTG | 286053 |
rs61204647 | in-del | -/A | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125341922 | AAAAAAAAAAAAAAA[-/A]CCTGTCTCTGCCCAT | 286053 |
rs61231328 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125238242 | AGAGCAGGCAGGGAA[C/T]GAGGTTATAGAAACT | 286053 |
rs61258982 | in-del | -/TTAA | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125192528 | TGTATATGGTAGCAA[-/TTAA]ATAGGGAAAAAACTG | 286053 |
rs61309806 | in-del | -/G | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125324943 | CAGTTGTGTTGGAGT[-/G]GGGGAGTAGAAGCCT | 286053 |
rs61550918 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125096238 | CCTTGGGTACAGTCA[C/T]AGGCCACAGCTAACT | 286053 |
rs61600410 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316689 | CTTCCTTCTTATCTT[-/T]CCTTCTTTCCTTCCT | 286053 |
rs61930535 | snp | A/G | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196554 | TTTTATGGCTGCATA[A/G]TATTTCATGGTGTAT | 286053 |
rs62520985 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125287957 | CCTTCTCAACTAACT[C/T]CTGTATCTACACCTA | 286053 |
rs62520997 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125318744 | GGCATGGAAAGGCAA[C/T]GATCCTTGAAGACAG | 286053 |
rs62520998 | snp | A/G | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125319712 | AAACTACCCAAAATG[A/G]AATAAAAAAAAGAAT | 286053 |
rs62520999 | snp | A/G | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125325324 | ATAAAATAAAATAAA[A/G]TAAAATAAAATAAAA | 286053 |
rs62521000 | snp | G/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125326388 | TTTGAGTAAAAATAG[G/T]CATTATATATATGTG | 286053 |
rs62521001 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125333696 | TTTTTTGTAGTTTTA[A/G]TAGAGACGGGGTTTC | 286053 |
rs62521002 | snp | G/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125335289 | GCGATTATGTGCCAA[G/T]CCCCATGTTTAGCGT | 286053 |
rs62521003 | snp | A/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125342966 | GAATACCCTTTTGGG[A/T]TTGTTCTCCTGACTT | 286053 |
rs62521017 | snp | A/C | 0.0252325 | 0.109451 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125344574 | ATGGTGAAACCCCGT[A/C]TCTACCAAAAATATA | 286053 |
rs62521018 | snp | A/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125349581 | TAGTGAGAGCTTGTA[A/T]TTAAAAAAAAAAAAA | 286053 |
rs62521019 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125354869 | AAAATCCAAAACCCA[A/C]AATGCTCCAAAATCC | 286053 |
rs62521020 | snp | A/T | 0.0252325 | 0.109451 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125356001 | AAGGGTCTTTCAGAG[A/T]GTCCATAAGGTCAAA | 286053 |
rs62521021 | snp | A/G | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125361062 | TAAAGCTGCCTTATG[A/G]TTTCCTTTTTTTTTT | 286053 |
rs62521022 | snp | A/T | | | utr-variant-3-prime | NSMCE2 | GRCh38.p7 | 8:125367098 | GTGTTCTATAATGTT[A/T]AATAAAACTTTGATC | 286053 |
rs62529098 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125100306 | CTCTGCAATGATTTG[C/T]GCACTTCATTCCTAC | 286053 |
rs62529099 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125146631 | AACCATCATTCTCAG[C/G/T]AAACTATCGCAAGGA | 286053 |
rs62529100 | snp | C/G | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125184586 | TTAGATTTCAAATGA[C/G]AGAACAAGCAAAATA | 286053 |
rs62529121 | snp | A/C | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125235847 | TTATTGCATATTTCA[A/C]TATTTTTGCTGTGGG | 286053 |
rs62529122 | snp | C/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125264495 | TACTGCAGTCTCTGC[C/T]TCCTGGGTTGAAACA | 286053 |
rs62529123 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272265 | ATGATCCGCCCGCCT[C/T]AGCCTCCCAAAGTGC | 286053 |
rs62529125 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125278835 | GCATAATATTGATAT[A/G]CCCTTGCTGCTGAAA | 286053 |
rs62529126 | snp | A/G | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125281876 | GAGCAACCACAACTG[A/G]CTAAGTGGGTGATTT | 286053 |
rs66561774 | snp | A/G | 0.135825 | 0.222405 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125228091 | ATAGTATCTTATACT[A/G]TGTATTGAGTCTTAA | 286053 |
rs66604371 | multinucleotide-polymorphism | ATCACACACC/GTCACACACT | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125146725 | CACAGGAAGGGGAAC[ATCACACACC/GTCACACACT]GGGGCCTGTTGTGAG | 286053 |
rs66826725 | snp | A/G | 0.13446 | 0.221699 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125156774 | GGTATAGTTTATCTC[A/G]GCTCTCTCATTATGC | 286053 |
rs66929016 | snp | C/T | 0.0930568 | 0.194599 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125217854 | GCCTTTTCCACTATA[C/T]TTAGTGGCAGTGACC | 286053 |
rs67042318 | in-del | -/AT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125236377 | AAACTATATATATAT[-/AT]ATCATATGATCCCAT | 286053 |
rs67144432 | in-del | -/AG | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125142793 | TTTTTAGTAGAGACG[-/AG]GTTTCTCCATGTTGG | 286053 |
rs67317762 | multinucleotide-polymorphism | CC/TT | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316719 | TTCTTTCTTTCCTTC[CC/TT]TTCCTTCCTTCCTTC | 286053 |
rs67359409 | in-del | -/AAAAA | 0 | 0 | downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125367543 | AAAAAAAAAAAAAAA[-/AAAAA]GAATGTCTTTCAAGT | 286053 |
rs67522578 | multinucleotide-polymorphism | AT/TA | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272716 | ATATATATATATATA[AT/TA]ATATATATATATACA | 286053 |
rs67631225 | in-del | -/T | 0.350109 | 0.229081 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125286316 | AATACCTTTTATTTA[-/T]TTTTTTTTTTTTTTG | 286053 |
rs67727948 | in-del | -/A | 0.5 | 0 | downstream-variant-500B | NSMCE2 | GRCh38.p7 | 8:125367531 | ACAGAGCAAGACTCT[-/A]AAAAAAAAAAAAAAA | 286053 |
rs67825410 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125301672 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTCCC | 286053 |
rs68114607 | in-del | -/T/TT | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125096635 | ACTGTGTGGAATCCT[-/T/TT]TTTTTTTTTTTTTTT | 286053 |
rs70977185 | in-del | -/ATTCCATGGCTG | 0.375 | 0.216506 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196563 | GTGGCACATACACAC[-/ATTCCATGGCTG]CATGGAATACTATGC | 286053 |
rs71295817 | in-del | -/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125107206 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTTGC | 286053 |
rs71295819 | in-del | -/TTTTTTTT | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125150444 | TTTTTTTTTTTTTTT[-/TTTTTTTT]GAGATGGAGTCTCAC | 286053 |
rs71295820 | in-del | -/AA | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125153081 | AAAAAAAAAAAAAAA[-/AA]GAATTGAACTTTTCC | 286053 |
rs71295823 | in-del | -/A | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125239629 | AAAAAAAAAAAAAAA[-/A]TTCAAACCAGGCACT | 286053 |
rs71295824 | in-del | -/AA | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125256959 | AAAAAAAAAAAAAAA[-/AA]GAGGGCTGAAGGTGA | 286053 |
rs71295825 | in-del | -/A | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125261752 | GTAAAAAAAAAAAAA[-/A]CAAAAACAAAACAGC | 286053 |
rs71295826 | in-del | -/AAATA | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125262097 | AAATAAAATAAAATA[-/AAATA]TAAAATAAATTGTAT | 286053 |
rs71295827 | in-del | -/T | | | intron-variant | NSMCE2 | GRCh38.p7 | 8:125266109 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTTTTGC | 286053 |
rs71295828 | in-del | -/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125267022 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTTGC | 286053 |
rs71295830 | in-del | -/CA | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272740 | ATATACACACACACA[-/CA]TATATATACACACGT | 286053 |
rs71295836 | in-del | -/TGTTTTGTTTT | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125314286 | TTTTTGTTTTGTTTT[-/TGTTTTGTTTT]GTTTTGTTTTTGTTT | 286053 |
rs71295839 | in-del | -/TTCCTTCC | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125316752 | TCCTTCCTTCCTTCC[-/TTCCTTCC]TTCCTTCCTTCCTTC | 286053 |
rs71295840 | in-del | -/A | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125324469 | AGAATACTACTCAGC[-/A]AAAAAAAAAAAAATG | 286053 |
rs71295841 | in-del | -/A | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125324536 | AAAAAAAAAAAAAAA[-/A]GAGCATATCCTATGT | 286053 |
rs71295843 | in-del | -/AAAAAA | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125327266 | GCAAGACTCCATCTC[-/AAAAAA]AAAAAAAAAAAAAAA | 286053 |
rs71295847 | in-del | -/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125333532 | TTTTTTTTTTTTTTT[-/T]GAGACGGAGTCTCGC | 286053 |
rs71295848 | in-del | -/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125340024 | TTTTTTTTTTTTTTT[-/T]GAGACGGAGTCTCGC | 286053 |
rs71355998 | snp | C/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196654 | GCACACATATGTTTA[C/T]TGCGGCACTATTCAC | 286053 |
rs71442141 | snp | C/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125196575 | CATGGTGTATATGTG[C/T]CACATTTTCTTAATC | 286053 |
rs71510323 | snp | C/T | 0 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125272728 | TATAATATATATATA[C/T]ACACACACACACATA | 286053 |
rs71510325 | snp | C/T | 0.469148 | 0.120308 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125286398 | GCTCACTGCAACCTC[C/T]GCCTCCTGGGTTCAA | 286053 |
rs71515999 | in-del | -/GT/GTGT | 0.371177 | 0.218669 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125183634 | ATTTATTACTCAGTG[-/GT/GTGT]GTGTGTGTGTGTGTG | 286053 |
rs71516763 | snp | A/G | 0.143959 | 0.226396 | upstream-variant-2KB, intron-variant | KIAA0196, NSMCE2 | GRCh38.p7 | 8:125093560 | TAAATAAATAAATAA[A/G]TAAATAAATAACATA | 286053 |
rs71516764 | snp | C/G | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125107474 | TGGGATTACAGGCAT[C/G]AGCCACCAGGCCTGG | 286053 |
rs71516765 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125112143 | ACAGCTTTTATAACT[A/G]GAGCCAACTATACCA | 286053 |
rs71516766 | snp | A/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125120265 | CAGAGAAGGGCAAGA[A/T]AGCATAAGGATATTT | 286053 |
rs71516767 | snp | A/G | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125142740 | CTCCCGAGTAGCTGG[A/G]ATTACAGGCATGCAC | 286053 |
rs71516768 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125154765 | TATAAGACAGTACAC[A/G]GATACACACTTTTTT | 286053 |
rs71516769 | snp | A/G | 0.135484 | 0.22223 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125218634 | CCAGGCTGGTCTTGA[A/G]CTCCTGACCTCAGGT | 286053 |
rs71516770 | snp | A/C | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125226895 | ATGGCACTGCTCTCC[A/C]AAACTTGTTCTGGCA | 286053 |
rs71516771 | snp | C/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125227003 | CCCAGCCCCCTTTGC[C/T]TAGGGACTCACCAGT | 286053 |
rs71516772 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125230132 | TAGTTCATTGACTTA[C/T]TCAGATTTCTTTGGA | 286053 |
rs71516773 | snp | C/T | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125256757 | GGTGAAACCCTGTCT[C/T]TATTAAAAATACAAA | 286053 |
rs71516774 | snp | C/G | 0.5 | 0 | intron-variant | NSMCE2 | GRCh38.p7 | 8:125256901 | GCACTCCAGCCTGGG[C/G]GACAAAGCAAGACTC | 286053 |