SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs717060 | snp | A/G | 0.00909072 | 0.0668036 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107897046 | tacatgaagcaatta[A/G]aatagtgcctaacat | 11043 |
rs742584 | snp | A/T | 0.257866 | 0.249876 | utr-variant-3-prime, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107930939 | TAAAGTAAAACCTGT[A/T]TTGAGAGTATGAAAG | 11043 |
rs1008503 | snp | A/G/T | 0.104127 | 0.20303 | intron-variant | MID2 | GRCh38.p7 | X:107831270 | CTCAGCTTCCTTCCC[A/G/T]TAGGTCAGACTCCGC | 11043 |
rs1158303 | snp | G/T | 0 | 0 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107923922 | AAACATGGAAACTCA[G/T]CCAAAGGGACACAta | 11043 |
rs1159681 | snp | A/C | 0 | 0 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107918225 | ACCGTAACATGTGAG[A/C]TAAACAACAGCTTTG | 11043 |
rs2050192 | snp | C/T | 0.00397613 | 0.0444101 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107900030 | GTCCTTAAGTGTTTT[C/T]TGAACAGGAAATACT | 11043 |
rs2236083 | snp | A/C | 0.152361 | 0.230145 | synonymous-codon | MID2 | GRCh38.p7 | X:107840845 | TCGCATTTTGGTATC[A/C]AGCTGCAGCTCTGGT | 11043 |
rs2267975 | snp | A/C | 0.0622094 | 0.165029 | intron-variant | MID2 | GRCh38.p7 | X:107865573 | AGGACTGAAAAGAAC[A/C]CTTTGGGGTGGGCGG | 11043 |
rs2273377 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | MID2 | GRCh38.p7 | X:107854835 | AGTTTTAGAAAGTCT[C/T]ATTCCTTTAGGATGC | 11043 |
rs2300099 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107919571 | CCATATGAAGAGCAA[C/T]TGAAAGAAAGGAAGA | 11043 |
rs2300100 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107914946 | gttatttccattttg[C/T]gaatgagaaagttgg | 11043 |
rs2300101 | snp | C/T | 0.443854 | 0.157862 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107898327 | CAGAAAAATAGAAAA[C/T]GTGCTTGGTTAAAGC | 11043 |
rs2300102 | snp | C/T | 0.022522 | 0.1037 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107896408 | AGTTACTGTCTCCCC[C/T]ATATTCTCTTTGTAA | 11043 |
rs2300103 | snp | A/T | 0.253421 | 0.249977 | intron-variant | MID2 | GRCh38.p7 | X:107867978 | TTAATTATATTTATG[A/T]CTATCCTAAGTCTCT | 11043 |
rs2300104 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | MID2 | GRCh38.p7 | X:107867842 | TACATCCTGTTCCAT[C/T]AAATCTGATTCTTCT | 11043 |
rs2300105 | snp | C/T | 0.445441 | 0.155894 | intron-variant | MID2 | GRCh38.p7 | X:107853951 | AAAACCATAACAATC[C/T]CACAAAGTAGAAGAT | 11043 |
rs2300106 | snp | G/T | 0.444914 | 0.156552 | intron-variant | MID2 | GRCh38.p7 | X:107847004 | AACCTCACTTCTTTG[G/T]GTTCAGTAATTCTTG | 11043 |
rs2300107 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | MID2 | GRCh38.p7 | X:107846965 | ATCTTTCCTCACCTA[C/T]ATTATATTTCTGTAA | 11043 |
rs2300108 | snp | A/C | 0.0660089 | 0.169255 | intron-variant | MID2 | GRCh38.p7 | X:107844468 | ATATATCATGAACTA[A/C]GATATATATTGGGAC | 11043 |
rs2344566 | snp | C/G | 0.399909 | 0.200068 | intron-variant | MID2 | GRCh38.p7 | X:107851780 | GCGTCCCCCACTACT[C/G]TCTTTCTACCCTCTG | 11043 |
rs2473631 | snp | A/T | 0 | 0 | intron-variant | MID2 | GRCh38.p7 | X:107893361 | GATATTAACAAAATA[A/T]AAACATTCTAGTAAT | 11043 |
rs2473632 | snp | A/C | 0 | 0 | intron-variant | MID2 | GRCh38.p7 | X:107893267 | GACTGTGTTTTTTAC[A/C]CGAAGTGAGAAGATC | 11043 |
rs2473635 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107922447 | AATTAAATGAATACA[G/T]ATGGGAAAATTGGGG | 11043 |
rs2500127 | snp | C/G | 0 | 0 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107915534 | ctgcactgcaacctg[C/G]gtgacacagcaagac | 11043 |
rs3060813 | in-del | -/CAAAA | | | intron-variant | MID2 | GRCh38.p7 | X:107884708 | caaaacaaaacaaaa[-/CAAAA]aCAGGGCAGATTAGA | 11043 |
rs3813784 | snp | C/T | 0.0358881 | 0.129059 | utr-variant-3-prime, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107931519 | TGGACCAATAGTGTC[C/T]CTCCTAGTGACAGAA | 11043 |
rs4036984 | snp | A/G | 0.44579 | 0.155455 | intron-variant | MID2 | GRCh38.p7 | X:107851767 | TCCATTTCCAGCTGC[A/G]TCCCCCACTACTCTC | 11043 |
rs4460524 | snp | C/T | 0 | 0 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107907047 | tcagatactctcttt[C/T]caatattctcaatcc | 11043 |
rs5903309 | in-del | -/C | | | intron-variant | MID2 | GRCh38.p7 | X:107852656 | GCTGGTCCTCATAAT[-/C]CCAGTTTGAGAAAAT | 11043 |
rs5903310 | in-del | -/AAAAC/AAAC | 0.0645269 | 0.16763 | intron-variant | MID2 | GRCh38.p7 | X:107884684 | GCTACAAAGAGACCA[-/AAAAC/AAAC]AAAACAAAACAAAAC | 11043 |
rs5916793 | snp | A/C | 0.0204249 | 0.0989712 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107904318 | ttcattgagctgtac[A/C]cttaggatttgggtg | 11043 |
rs5917074 | snp | A/T | 0.432112 | 0.171275 | intron-variant | MID2 | GRCh38.p7 | X:107845525 | CACACACACACACAC[A/T]CTCTCTCTCTCTCTC | 11043 |
rs5917075 | snp | C/T | 0.0323082 | 0.122924 | intron-variant | MID2 | GRCh38.p7 | X:107884747 | TGGCAGAAGTCTTGG[C/T]CTtggagttaggatg | 11043 |
rs5962410 | snp | C/T | 0.435581 | 0.16751 | intron-variant | MID2 | GRCh38.p7 | X:107829818 | TCGTCTGGCATGTTG[C/T]ACCCTGCAAGGCCAC | 11043 |
rs5962411 | snp | C/T | 0.0470497 | 0.145984 | intron-variant | MID2 | GRCh38.p7 | X:107845980 | TGAGTGTGTATATTC[C/T]TGCATAAATATGTGG | 11043 |
rs5962412 | snp | A/T | 0.0470497 | 0.145984 | intron-variant | MID2 | GRCh38.p7 | X:107846003 | ATATGTGGCTGAGAA[A/T]GACTCTGTGTCTGTG | 11043 |
rs5962413 | snp | A/G | 0.151636 | 0.229836 | intron-variant | MID2 | GRCh38.p7 | X:107854911 | ACGGTGATGATGGAC[A/G]GTGGGGGGATAATAG | 11043 |
rs5962414 | snp | A/G | 0.150308 | 0.229263 | intron-variant | MID2 | GRCh38.p7 | X:107854966 | TCCAAACAGCAGGCA[A/G]TATGAAAATCAGACA | 11043 |
rs5962415 | snp | A/G | 0.443854 | 0.157862 | intron-variant | MID2 | GRCh38.p7 | X:107882892 | ttctactataaagac[A/G]catgcacacatatgt | 11043 |
rs5962896 | snp | C/G | 0.05658 | 0.158394 | intron-variant | MID2 | GRCh38.p7 | X:107829578 | TAGCACCTAGTAGCA[C/G]AGTCAACAATATTAA | 11043 |
rs5962897 | snp | A/G | 0.0525796 | 0.153379 | intron-variant | MID2 | GRCh38.p7 | X:107840042 | CTCAGTTTACTAGGA[A/G]TAGAATGGAACGGAA | 11043 |
rs5962898 | snp | A/T | 0.05658 | 0.158394 | intron-variant | MID2 | GRCh38.p7 | X:107843491 | CAGATTTTGAATAGT[A/T]CCCCTTTCATATTTT | 11043 |
rs5962899 | snp | A/G | 0 | 0 | intron-variant | MID2 | GRCh38.p7 | X:107847313 | AAGTGGGAAATTCCA[A/G]TTCAGTATGGTAAGT | 11043 |
rs5962901 | snp | A/G | 0.151194 | 0.229646 | intron-variant | MID2 | GRCh38.p7 | X:107859068 | TCTCTTTAGAGTTCA[A/G]ACTTCAGATGGGCTG | 11043 |
rs5962902 | snp | C/T | 0.085528 | 0.188279 | intron-variant | MID2 | GRCh38.p7 | X:107861045 | TGGTTCCTGGACCCA[C/T]TGTGAGGATGACTTG | 11043 |
rs5962903 | snp | C/T | 0.445616 | 0.155675 | intron-variant | MID2 | GRCh38.p7 | X:107865764 | GGCACAAAACAATCA[C/T]TGGCTTTGGAATAAT | 11043 |
rs5962904 | snp | C/T | 0.445441 | 0.155894 | intron-variant | MID2 | GRCh38.p7 | X:107868178 | AGCAAGGTACTGGCA[C/T]GTAGAGAGTAACTGA | 11043 |
rs5962906 | snp | A/G | 0.444562 | 0.156989 | intron-variant | MID2 | GRCh38.p7 | X:107871726 | agtctagctgtcccc[A/G]gctggactcctcttc | 11043 |
rs5962907 | snp | G/T | 0.0220041 | 0.102557 | intron-variant | MID2 | GRCh38.p7 | X:107871783 | tgaagtcaagctgct[G/T]ctttccaacttccaa | 11043 |
rs5962909 | snp | A/G | 0.308702 | 0.24301 | intron-variant | MID2 | GRCh38.p7 | X:107887856 | gtttagtcttgggag[A/G]gtgtatgtgttgagg | 11043 |
rs5962910 | snp | A/G | 0.445266 | 0.156113 | intron-variant | MID2 | GRCh38.p7 | X:107893163 | ACGGCTTTCTGAAAA[A/G]CAGTGCTATTATTGA | 11043 |
rs5962911 | snp | C/T | 0.313263 | 0.241863 | intron-variant | MID2 | GRCh38.p7 | X:107893858 | TGTCCTTTTGCCATC[C/T]GTACTTTATATGCTG | 11043 |
rs6523981 | snp | A/G | 0.443677 | 0.15808 | intron-variant | MID2 | GRCh38.p7 | X:107881506 | TTTCTTCTCTCTGGT[A/G]TGTCCTTCAAAACTT | 11043 |
rs6523982 | snp | A/C | 0.241753 | 0.249864 | intron-variant | MID2 | GRCh38.p7 | X:107888942 | aggctaggattgcag[A/C]ccctgcctttttttg | 11043 |
rs6523983 | snp | A/C/G | 0.445796 | 0.157699 | intron-variant | MID2 | GRCh38.p7 | X:107891081 | gtgaggcgatgcctc[A/C/G]ccctgcttcggctca | 11043 |
rs6523985 | snp | A/C | 0.444386 | 0.157208 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107906557 | cagtttttaactata[A/C]cctctacttaacaac | 11043 |
rs6616669 | snp | C/T | 0 | 0 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107910939 | gctcactgcaatctc[C/T]gcctcccagattcaa | 11043 |
rs6622267 | snp | C/G | 0.0204488 | 0.0990265 | intron-variant | MID2 | GRCh38.p7 | X:107835150 | aggagccttttgtga[C/G]tggcttcttttactt | 11043 |
rs6622268 | snp | A/G | 0.438029 | 0.164757 | intron-variant | MID2 | GRCh38.p7 | X:107838787 | TGATGACAAGATAAT[A/G]AACAAAAGCTACTCA | 11043 |
rs6622271 | snp | C/T | 0 | 0 | intron-variant | MID2 | GRCh38.p7 | X:107846849 | AATATTTGAAAGGAG[C/T]TAACAATCGTTTGTT | 11043 |
rs6622274 | snp | C/T | | | intron-variant | MID2 | GRCh38.p7 | X:107893149 | TCTTTCATGTTCTTA[C/T]GGCTTTCTGAAAAAC | 11043 |
rs6622275 | snp | A/G | | | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107897917 | CTTGATAATTCATCA[A/G]ATGTCCAATTTACCT | 11043 |
rs6652967 | snp | C/T | 0.444562 | 0.156989 | intron-variant | MID2 | GRCh38.p7 | X:107871317 | CTTGCTTGGCCCCAC[C/T]GTGTTCCACGCCTTG | 11043 |
rs6652968 | snp | A/G | 0.444562 | 0.156989 | intron-variant | MID2 | GRCh38.p7 | X:107871499 | ttagctttgctgtcc[A/G]tgaatggcttaagtg | 11043 |
rs7051357 | snp | A/C | | | intron-variant | MID2 | GRCh38.p7 | X:107857335 | gcccaggctagagtg[A/C]agtggcacaatctcg | 11043 |
rs7053430 | snp | A/G | 0.445441 | 0.155894 | intron-variant | MID2 | GRCh38.p7 | X:107859919 | ttgggcccaaataat[A/G]aagagccttgtaggc | 11043 |
rs7053643 | snp | C/T | 0.103655 | 0.20269 | intron-variant | MID2 | GRCh38.p7 | X:107836400 | ctgggactacaggca[C/T]gcgccactacgcctg | 11043 |
rs7053850 | snp | A/G | 0.104127 | 0.20303 | intron-variant | MID2 | GRCh38.p7 | X:107854206 | CTTCATCATAAGTTG[A/G]GGGACATGTGTAATA | 11043 |
rs7054585 | snp | A/C/G | 0.151636 | 0.229836 | intron-variant | MID2 | GRCh38.p7 | X:107854452 | ATTATTAATTTGTAC[A/C/G]TAGATTAGTGCTTGG | 11043 |
rs7055611 | snp | A/G | 0.103655 | 0.20269 | intron-variant | MID2 | GRCh38.p7 | X:107872254 | tctaggtgcaaagaa[A/G]caagttttacagggt | 11043 |
rs7060291 | snp | A/G | 0.0440191 | 0.141675 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107903048 | aattctctacgcctc[A/G]gtttccccgtatgtg | 11043 |
rs7066710 | snp | C/G | 0.151636 | 0.229836 | intron-variant | MID2 | GRCh38.p7 | X:107853141 | CTCTTTTTCACATAA[C/G]GAATGGGAAACAGTA | 11043 |
rs7067117 | snp | A/G | 0.0214859 | 0.101397 | intron-variant | MID2 | GRCh38.p7 | X:107853188 | ACATGCTAGAATTCC[A/G]GCTACTGTTGTAACA | 11043 |
rs7878008 | snp | A/G | 0 | 0 | intron-variant | MID2 | GRCh38.p7 | X:107841460 | TCTCTAATAAAATAG[A/G]TGACTTTTCCTATAT | 11043 |
rs7879230 | snp | C/T | 0.33977 | 0.233327 | intron-variant | MID2 | GRCh38.p7 | X:107829243 | TTGACTGGGTGTAAG[C/T]AGGAATCTTAGCTTA | 11043 |
rs7879425 | snp | A/G | 0.339469 | 0.233442 | intron-variant | MID2 | GRCh38.p7 | X:107829196 | TACTTTTCAAAGAAA[A/G]CACTTCCTTTACCTT | 11043 |
rs7879884 | snp | C/G | 0.00791544 | 0.0624105 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107924611 | GGGAGCAGTGGTACT[C/G]GGTAGAGGAGCTATA | 11043 |
rs7880389 | snp | C/G | 0.327548 | 0.237668 | upstream-variant-2KB, utr-variant-5-prime | MID2 | GRCh38.p7 | X:107824101 | ttttttgaggaacct[C/G]catactattttccat | 11043 |
rs7880672 | snp | C/T | 0.327548 | 0.237668 | upstream-variant-2KB, utr-variant-5-prime | MID2 | GRCh38.p7 | X:107824314 | ctcttgcctcagcat[C/T]ccctcctgagtagct | 11043 |
rs7882633 | snp | A/T | 0.154285 | 0.230951 | intron-variant | MID2 | GRCh38.p7 | X:107833431 | tatatatatatatat[A/T]tTTTTTAAAAACCTA | 11043 |
rs7882634 | snp | A/T | | | intron-variant | MID2 | GRCh38.p7 | X:107833433 | tatatatatatattt[A/T]ttttaaaaaCCTACA | 11043 |
rs7883542 | snp | A/G | 0.313263 | 0.241863 | intron-variant | MID2 | GRCh38.p7 | X:107881863 | ggaattattttattc[A/G]ctgtgattatgcaaa | 11043 |
rs7885256 | snp | A/C | 0.403433 | 0.197379 | intron-variant | MID2 | GRCh38.p7 | X:107839734 | TCTTAAAATTTCTGG[A/C]ACTTTGCTAATTTCT | 11043 |
rs7887181 | snp | C/T | 0.0869739 | 0.189532 | intron-variant | MID2 | GRCh38.p7 | X:107834958 | aagttgtgcaatcat[C/T]gtcactatctaattt | 11043 |
rs7888271 | snp | A/G | 0.0965482 | 0.197364 | downstream-variant-500B, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107931823 | ACTTTGATTTCAGGA[A/G]CATGATATGGTCAAG | 11043 |
rs7888338 | snp | A/G | 0.016289 | 0.0887646 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107912871 | CTGAAATTTTCCCCC[A/G]CCATTATGCATTGTA | 11043 |
rs9699225 | snp | G/T | 0.104127 | 0.20303 | intron-variant | MID2 | GRCh38.p7 | X:107842656 | CAATGACTATGGTTT[G/T]TGCCTCTTTTGGTTA | 11043 |
rs9919100 | snp | C/T | 0.0525796 | 0.153379 | intron-variant | MID2 | GRCh38.p7 | X:107854308 | gggcgaaatgagata[C/T]tgcctatgaaatact | 11043 |
rs10481933 | snp | C/G | 0.445441 | 0.155894 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107909326 | tagctggtaggaaca[C/G]acactattgctagac | 11043 |
rs11092600 | snp | A/G | 0.0194105 | 0.0965841 | intron-variant | MID2 | GRCh38.p7 | X:107849033 | AGACTCAGGTTTGGG[A/G]TGAATTGGCCTTTCT | 11043 |
rs11541084 | snp | C/G | | | utr-variant-5-prime, intron-variant | MID2 | GRCh38.p7 | X:107826053 | TCCGCCTCCCTTTTG[C/G]AAGGGATTGCCTTTT | 11043 |
rs11797581 | snp | G/T | | | intron-variant | MID2 | GRCh38.p7 | X:107871961 | cactttgggacacgg[G/T]tccaggcttgagggc | 11043 |
rs11797607 | snp | A/G | 0.00938946 | 0.0678717 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107911229 | gactggtgacctcta[A/G]ctctgggaaatgttc | 11043 |
rs12011005 | snp | C/G | 0.0399626 | 0.135589 | intron-variant | MID2 | GRCh38.p7 | X:107875258 | aggtacttgagatag[C/G]agggtatacagattg | 11043 |
rs12012633 | snp | C/T | 0.0399626 | 0.135589 | intron-variant | MID2 | GRCh38.p7 | X:107836542 | aggcgtgagccacca[C/T]gcccagccTACtttt | 11043 |
rs12012669 | snp | A/C | 0.0540818 | 0.155294 | intron-variant | MID2 | GRCh38.p7 | X:107887177 | tgaataggagtggtg[A/C]gagagggcatccctg | 11043 |
rs12013286 | snp | A/C | 0.0333324 | 0.12472 | utr-variant-3-prime, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107929811 | ACTTGATGATGCATC[A/C]CTCTTTAGAGATCCA | 11043 |
rs12013687 | snp | A/G | 0.0245906 | 0.108123 | intron-variant | MID2 | GRCh38.p7 | X:107887671 | attccctctttttct[A/G]ttgattggaatagtt | 11043 |
rs12387575 | snp | G/T | 0.00317376 | 0.039709 | intron-variant | MID2 | GRCh38.p7 | X:107884450 | gtttctattttacca[G/T]tcagaaagatagctc | 11043 |
rs12394544 | snp | G/T | 0.0470497 | 0.145984 | intron-variant | MID2 | GRCh38.p7 | X:107857207 | GGACCCTACAGGATG[G/T]CTTATGGAAGGCCAT | 11043 |
rs12835030 | snp | G/T | 0 | 0 | intron-variant | MID2 | GRCh38.p7 | X:107877102 | tgcagccttccctga[G/T]atggcaaaccggagg | 11043 |
rs12835095 | snp | C/G | | | intron-variant | MID2 | GRCh38.p7 | X:107877277 | tgaggccaagacagt[C/G]cttcctgcagatcac | 11043 |
rs12835300 | snp | C/G | 0 | 0 | intron-variant | MID2 | GRCh38.p7 | X:107877237 | gtccaactacacgat[C/G]gtattgaaatgaatg | 11043 |
rs12836590 | snp | C/T | 0 | 0 | intron-variant | MID2 | GRCh38.p7 | X:107877236 | ggtccaactacacga[C/T]ggtattgaaatgaat | 11043 |
rs12839981 | snp | C/T | 0.05658 | 0.158394 | intron-variant | MID2 | GRCh38.p7 | X:107881146 | ATGCTGTTAGAGTGC[C/T]ACTAAATTCAGTCAC | 11043 |
rs12841876 | snp | G/T | 0 | 0 | utr-variant-3-prime, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107928858 | AGCAGCAATGTCATC[G/T]TTTTTGATTTTAAAT | 11043 |
rs12842315 | snp | C/T | 0.252677 | 0.249986 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107898967 | TCATCTACTATTTCA[C/T]ATATCTTGTTCCATC | 11043 |
rs12844942 | snp | A/G | 0.0650211 | 0.168175 | utr-variant-5-prime | MID2 | GRCh38.p7 | X:107823705 | tccttttccctcctc[A/G]cagtccctgacaacc | 11043 |
rs12845616 | snp | C/G | 0.0645269 | 0.16763 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107903379 | GTTTTGATGTAGCCA[C/G]TATCCCAAAATAGGA | 11043 |
rs12847345 | snp | A/T | 0.340668 | 0.232979 | intron-variant | MID2 | GRCh38.p7 | X:107833429 | TATATATATATATAT[A/T]TTTTTTTTAAAAACC | 11043 |
rs12849503 | snp | C/G | | | utr-variant-3-prime, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107930494 | CACTCAAAGCTAAGC[C/G]TACTTAAAAAAGTGG | 11043 |
rs12849510 | snp | A/C | 0.0763223 | 0.17983 | missense, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107916061 | TCAATTTTAATGATG[A/C]CTTTGAAAACTTTGC | 11043 |
rs12850318 | snp | A/G | 0.0650211 | 0.168175 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107924729 | CTTGGGAGGATGTTA[A/G]TGAAGAGTTTTCTCT | 11043 |
rs12850680 | snp | A/G | 0.444209 | 0.157426 | intron-variant, nc-transcript-variant | MID2, LOC101928335 | GRCh38.p7 | X:107895030 | TAAGTTTAATCTTAC[A/G]TAAAAGTTGCTAAAA | 11043 |
rs12850918 | snp | C/T | 0 | 0 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107917853 | GCAAGTTGTATATTT[C/T]CTTGCTGGGCAGTTG | 11043 |
rs12851669 | snp | G/T | | | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107916318 | ATGATTTATGATTTG[G/T]TAACTATTTCTAGGG | 11043 |
rs12851877 | snp | G/T | | | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107916394 | TTGCTGATAGATTTG[G/T]CCTTATGAATCTAAC | 11043 |
rs12852580 | snp | A/G | 0.054582 | 0.155922 | intron-variant | MID2 | GRCh38.p7 | X:107830607 | ATAAATGAAATTTTG[A/G]TACCAAGATGGTGTT | 11043 |
rs12853228 | snp | C/G | 0.252677 | 0.249986 | intron-variant | MID2 | GRCh38.p7 | X:107882774 | tgtaaactagttcaa[C/G]cattgtggaagacag | 11043 |
rs12854056 | snp | A/C | 0 | 0 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107913171 | ATTTAGATATATTTC[A/C]CAAACATGATATGCT | 11043 |
rs12856043 | snp | A/G | 0 | 0 | intron-variant | MID2 | GRCh38.p7 | X:107891832 | TACTCCCTCAGCTTA[A/G]AAGCAACATAGGCTC | 11043 |
rs12856401 | snp | A/G | | | intron-variant | MID2 | GRCh38.p7 | X:107891908 | GTTGGGCTGGAATCA[A/G]ACTGTTTTCTGTCTG | 11043 |
rs12857560 | snp | C/T | 0 | 0 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107921813 | tctgggtccttataa[C/T]attcccccatcattt | 11043 |
rs12861437 | snp | C/T | 0.310663 | 0.242528 | intron-variant | MID2 | GRCh38.p7 | X:107888686 | tgttaactttctgcc[C/T]gttgatttgtctaat | 11043 |
rs12863681 | snp | C/T | 0.30903 | 0.242931 | intron-variant | MID2 | GRCh38.p7 | X:107859184 | GTCTGGCTGCTTCTC[C/T]AAGCATAAAATATAA | 11043 |
rs13441106 | snp | A/G | | | intron-variant | MID2 | GRCh38.p7 | X:107887705 | gaaggaatggtacca[A/G]ctcctccttgtacct | 11043 |
rs17254214 | snp | A/T | 0.0560809 | 0.157783 | intron-variant | MID2 | GRCh38.p7 | X:107840332 | CAGGGTCTCAGCCTT[A/T]TCTTAGTCTAGGAAA | 11043 |
rs17254228 | snp | C/T | 0.126432 | 0.217327 | intron-variant | MID2 | GRCh38.p7 | X:107861889 | TGTAGCCTTAGTTTC[C/T]ACAACTTGCCTGTCC | 11043 |
rs17280029 | snp | A/G | 0.00738971 | 0.0603345 | intron-variant | MID2 | GRCh38.p7 | X:107838520 | CAAACATCTGAATCT[A/G]CTAAACCAACTGAGT | 11043 |
rs17320095 | snp | G/T | 0.0266548 | 0.112325 | intron-variant | MID2 | GRCh38.p7 | X:107865995 | GGATTAGAGAAGAGG[G/T]TGAGTGACCTAGGCA | 11043 |
rs17326703 | snp | A/G | 0.0115877 | 0.0752302 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107915710 | GCTGTCTGCCAGATG[A/G]AAAATGATGCAGAGG | 11043 |
rs17326710 | snp | A/G | 0.148534 | 0.228483 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107918269 | GAATTGGAGCAAGAC[A/G]AAACAGAGTAGGAAC | 11043 |
rs28435208 | snp | C/T | 0 | 0 | intron-variant | MID2 | GRCh38.p7 | X:107870612 | TATAATTAATATCTC[C/T]CCAATGGTGTGCTGG | 11043 |
rs28444788 | snp | A/G | 0.241372 | 0.249851 | intron-variant | MID2 | GRCh38.p7 | X:107868003 | AATTAAGGCAAATGG[A/G]GATCTTTTTGAGGTG | 11043 |
rs28477515 | snp | G/T | 0 | 0 | intron-variant | MID2 | GRCh38.p7 | X:107829410 | ATTTAAGTTGAGGCT[G/T]GAATCATTTCTAATG | 11043 |
rs28553396 | snp | C/G | | | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107925210 | GACTTCTGCTTCCAT[C/G]TGCTTCCATGTTCTT | 11043 |
rs28599746 | snp | C/T | 0.0530806 | 0.154022 | intron-variant | MID2 | GRCh38.p7 | X:107868219 | ATGGATGAGGTCACC[C/T]AAGTCAGTGTGCTAG | 11043 |
rs28749769 | snp | G/T | | | intron-variant | MID2 | GRCh38.p7 | X:107887766 | TCCTGGACTTTTTTT[G/T]GTTTGTAAGCTATTA | 11043 |
rs28897135 | snp | G/T | | | intron-variant | MID2 | GRCh38.p7 | X:107887768 | CTGGACTTTTTTTGG[G/T]TTGTAAGCTATTAAT | 11043 |
rs34031869 | in-del | -/C | | | intron-variant | MID2 | GRCh38.p7 | X:107885415 | TGAGAATGATGGTTT[-/C]CCAGCTTCATCCATG | 11043 |
rs34093911 | in-del | -/C | | | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107912347 | ATCTCTGCTCTCCAA[-/C]CCTCTGAAATGTTTT | 11043 |
rs34128262 | in-del | -/C | | | intron-variant | MID2 | GRCh38.p7 | X:107885309 | CGGTGTGTGATGTTT[-/C]CCCTTCCTGTGTCCA | 11043 |
rs34185698 | in-del | -/C | | | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107925180 | CTTTCCTAGAACTTT[-/C]CCCCTGCTCTGTCTG | 11043 |
rs34434823 | snp | G/T | 0.408163 | 0.193609 | intron-variant | MID2 | GRCh38.p7 | X:107845039 | GCTTTGGATCTCATC[G/T]AAGAAGATATAAATC | 11043 |
rs34444789 | snp | A/T | 0.0645269 | 0.16763 | intron-variant | MID2 | GRCh38.p7 | X:107874492 | CTTACTTAGGTAGCC[A/T]ACAGGCTGCTGGGCT | 11043 |
rs34462086 | in-del | -/G | | | intron-variant, nc-transcript-variant | MID2, LOC101928335 | GRCh38.p7 | X:107895225 | CACTCAACTTTTTTT[-/G]GGGGGGGGGGTGGAT | 11043 |
rs34463108 | in-del | -/C | | | intron-variant | MID2 | GRCh38.p7 | X:107852462 | TCCTGTATTCTTCTT[-/C]CCTTCCCCTTTTCTT | 11043 |
rs34467810 | snp | G/T | 0.444444 | 0.157135 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107902407 | TAAATGAATCTCTTA[G/T]TCTCAGATAAAGGAG | 11043 |
rs34853484 | in-del | -/AT | 0.0655152 | 0.168717 | intron-variant | MID2 | GRCh38.p7 | X:107840244 | TACACTGGATGTCAC[-/AT]AGAAGCAGCCCTACA | 11043 |
rs35034219 | in-del | -/A | | | intron-variant | MID2 | GRCh38.p7 | X:107842553 | CATTGTAACTTCTGT[-/A]AAAAGTATAATGTTG | 11043 |
rs35061896 | in-del | -/C | | | intron-variant | MID2 | GRCh38.p7 | X:107885339 | TGTGTTCTCACTGTT[-/C]CAGTTCCCACCTATG | 11043 |
rs35206465 | in-del | -/GA/GAGA | | | intron-variant | MID2 | GRCh38.p7 | X:107885097 | TTTTTTTCCAGGAGA[-/GA/GAGA]ATCTCTTATTTATTT | 11043 |
rs35217984 | in-del | -/G | | | intron-variant | MID2 | GRCh38.p7 | X:107852508 | GATTGAGATGGTAGT[-/G]GGGATTAAAGGAGGC | 11043 |
rs35256046 | in-del | -/T | | | intron-variant | MID2 | GRCh38.p7 | X:107831693 | ATACATATATTGCCA[-/T]TTTTTATTGTGTAGA | 11043 |
rs35310046 | in-del | -/C | | | splice-acceptor-variant, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107917505 | CACCTTTCCTTACAG[-/C]CCCCAAACCCACCAT | 11043 |
rs35349478 | in-del | -/TCT | 0.434627 | 0.168562 | intron-variant | MID2 | GRCh38.p7 | X:107835654 | TTGGCCATTTGTATA[-/TCT]TCTTTGGAAAAAATC | 11043 |
rs35451756 | in-del | -/A | 0.358671 | 0.225146 | intron-variant | MID2 | GRCh38.p7 | X:107837539 | AGAAACATGCTGTTT[-/A]AAAAAAAAAAACTCT | 11043 |
rs35453729 | in-del | -/T | 0 | 0 | intron-variant | MID2 | GRCh38.p7 | X:107836554 | CCACGCCCAGCCTAC[-/T]TTTTTTTTTTTTTAA | 11043 |
rs35488899 | snp | A/C | | | intron-variant | MID2 | GRCh38.p7 | X:107840285 | GAAGTGAAATAGAGA[A/C]CAATATTGGAGAATA | 11043 |
rs35501455 | in-del | -/C | | | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107906421 | TAGCTTCTTTAACAT[-/C]CCCCTCCAACAGTGA | 11043 |
rs35557108 | in-del | -/C | | | intron-variant | MID2 | GRCh38.p7 | X:107836661 | TGCTTAGATAACCAG[-/C]AAAGGTAGGGGAAAT | 11043 |
rs35580835 | in-del | -/T | 0.0645269 | 0.16763 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107899741 | TTCAAGGAGGATAGA[-/T]TTTTTTTTCCACAGA | 11043 |
rs35627322 | in-del | -/A | | | intron-variant | MID2 | GRCh38.p7 | X:107877690 | TTCCCAGGGCTTTAT[-/A]CTATGCCGTGGAGCA | 11043 |
rs35706580 | snp | C/G | 0.348932 | 0.229592 | intron-variant | MID2 | GRCh38.p7 | X:107838984 | GGCTTGGTGGCATAC[C/G]CCTGGAGTTCCAGGA | 11043 |
rs35716955 | snp | C/T | | | missense | MID2 | GRCh38.p7 | X:107841015 | GTGGGCCCAATTCCC[C/T]TAGTGAGAGCCGCCG | 11043 |
rs35917999 | in-del | -/T | | | intron-variant | MID2 | GRCh38.p7 | X:107890745 | GCAGGCAGGCCTCCT[-/T]TGAGCTGCGGTGGGC | 11043 |
rs57100746 | in-del | -/CACACACACACACACACA | | | intron-variant | MID2 | GRCh38.p7 | X:107866460 | ACACACACACACACA[-/CACACACACACACACACA]ACACTGACCTACAGT | 11043 |
rs57472634 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107877931 | GCAGTTATCAGCCAG[C/T]GGGGCCACTCCTCCA | 11043 |
rs57606108 | snp | A/G | | | utr-variant-3-prime, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107930776 | AACATTTTCAAAGAA[A/G]GTGACTGCATAAGCT | 11043 |
rs57908841 | snp | C/T | 0.043513 | 0.140937 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107914551 | TTCCCTTACAACTAG[C/T]TCACCATAAAAGTTT | 11043 |
rs58140023 | in-del | -/A | | | intron-variant | MID2 | GRCh38.p7 | X:107836986 | TGAGAATCTTTTGAA[-/A]GCTATGGGCAACCCT | 11043 |
rs58256342 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | MID2 | GRCh38.p7 | X:107889946 | TCATCACATAGTTCT[C/T]GTGCCATGGTTTTCA | 11043 |
rs58268309 | snp | C/T | 0.018891 | 0.0953342 | utr-variant-5-prime | MID2 | GRCh38.p7 | X:107823072 | AATTCCTCATTTCCT[C/T]TCCCTTCAGTTCCTG | 11043 |
rs58705027 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | MID2 | GRCh38.p7 | X:107870621 | TATCTCTCCAATGGT[A/G]TGCTGGTGCTGACTT | 11043 |
rs58821735 | snp | A/G | | | intron-variant | MID2 | GRCh38.p7 | X:107828557 | GGTCAAGCTGTCTGA[A/G]GGCCTCGCCAAGTGC | 11043 |
rs59157949 | in-del | -/ATAT | | | utr-variant-5-prime | MID2 | GRCh38.p7 | X:107823407 | TATATATATATATAT[-/ATAT]GTATTATCATACAAA | 11043 |
rs59323042 | snp | A/G | 0.0525796 | 0.153379 | upstream-variant-2KB, utr-variant-5-prime | MID2 | GRCh38.p7 | X:107824976 | ACAATGATGGGAGGC[A/G]TGTGTGTGTGTGTGC | 11043 |
rs59622391 | in-del | -/TGTG | | | upstream-variant-2KB, utr-variant-5-prime | MID2 | GRCh38.p7 | X:107824413 | GTGTGTGTGTGTGTG[-/TGTG]ACCATCCTAATGGAT | 11043 |
rs59684590 | snp | C/T | | | intron-variant | MID2 | GRCh38.p7 | X:107836391 | CCCGAGTAGCTGGGA[C/T]TACAGGCATGCGCCA | 11043 |
rs59717985 | in-del | -/T | | | intron-variant | MID2 | GRCh38.p7 | X:107870771 | TTTTTTTTTTTTTTT[-/T]GAGAGCCAATTGTTA | 11043 |
rs60028449 | snp | C/T | 0.0440191 | 0.141675 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107902602 | TCACTCAGCAACAGA[C/T]ATATTTTATTTCAGT | 11043 |
rs60560473 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107906806 | GGCCAGGCTGGTTTC[A/G]AATTCCTGGCCTCAA | 11043 |
rs60861461 | in-del | -/A | | | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107896706 | AAGTCAGGAAGGAAA[-/A]TACACAAAATATTTG | 11043 |
rs61105394 | snp | A/G | 0.00896606 | 0.0663524 | intron-variant | MID2 | GRCh38.p7 | X:107885391 | GTTTTTTGTCTTTGC[A/G]ATAGTTTGCTGAGAA | 11043 |
rs61320155 | snp | C/T | | | intron-variant | MID2 | GRCh38.p7 | X:107851591 | TGCTAGGTTAATCTC[C/T]TAAATGCAGCCCTGA | 11043 |
rs61752720 | snp | A/G | 2.29584e-05 | 0.00338802 | missense, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107924475 | AAGCCGGCAGCCGGA[A/G]CAGTGAACCTACCCG | 11043 |
rs66845371 | snp | A/C | 0.431525 | 0.171897 | upstream-variant-2KB, utr-variant-5-prime | MID2 | GRCh38.p7 | X:107825663 | CACACACATTTAGCT[A/C]TCTCTGTCGCTCTGT | 11043 |
rs66939798 | snp | A/C | 0.338568 | 0.233786 | intron-variant | MID2 | GRCh38.p7 | X:107826977 | CGAGTCTCCGTCTGG[A/C]TGGTTCCTTATTTCT | 11043 |
rs66964475 | in-del | -/T | 0.151636 | 0.229836 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107898529 | CTCATACACCTTTAA[-/T]TGTATTCTATTATAT | 11043 |
rs72282624 | in-del | -/TATA | 0.391194 | 0.206311 | utr-variant-5-prime | MID2 | GRCh38.p7 | X:107823390 | TATCTGAGATTGTTT[-/TATA]TATATATATATATAT | 11043 |
rs72618358 | snp | C/G | | | intron-variant | MID2 | GRCh38.p7 | X:107873137 | GGAGGTACTTAGGGA[C/G]TCCAAAGCAAGGAAT | 11043 |
rs72618359 | snp | G/T | 0.00844089 | 0.0644143 | intron-variant, nc-transcript-variant | MID2, LOC101928335 | GRCh38.p7 | X:107896097 | ACACCTGTAATCCTA[G/T]CACTTTAGGAGGCCG | 11043 |
rs73249880 | snp | A/C/T | 0.0194105 | 0.0965841 | upstream-variant-2KB, utr-variant-5-prime | MID2 | GRCh38.p7 | X:107824023 | TTGAGATCCTGTTTT[A/C/T]TATTTGCTTGGATAT | 11043 |
rs73249881 | snp | A/T | 0.0026455 | 0.0362733 | intron-variant | MID2 | GRCh38.p7 | X:107830792 | GCTGTAATTATCTTC[A/T]TGTACAGATAGCTAA | 11043 |
rs73249882 | snp | A/C | 0.113965 | 0.209748 | intron-variant | MID2 | GRCh38.p7 | X:107849488 | AAGTGAAAAAAAAAA[A/C]CCAGCAATTATTTGA | 11043 |
rs73249883 | snp | A/G | 0.172968 | 0.237836 | intron-variant | MID2 | GRCh38.p7 | X:107855176 | CTTCATCCCCTGCCC[A/G]TGGTCCTATCTATAC | 11043 |
rs73249884 | snp | A/G | 0.173397 | 0.237975 | intron-variant | MID2 | GRCh38.p7 | X:107871386 | GGCAAGCGCTTTTGG[A/G]TGCTGGCAGGAGCGA | 11043 |
rs73249885 | snp | C/G | 0.172968 | 0.237836 | intron-variant | MID2 | GRCh38.p7 | X:107875391 | TTACAAGGGCTGTTG[C/G]AGGGTTTGAGGAGGC | 11043 |
rs73249887 | snp | A/T | 0.0363984 | 0.129901 | intron-variant | MID2 | GRCh38.p7 | X:107884115 | TACACAAGTTATAAG[A/T]TCCAAATCTACCGCA | 11043 |
rs73251746 | snp | A/C | 0.17254 | 0.237697 | intron-variant, nc-transcript-variant | MID2, LOC101928335 | GRCh38.p7 | X:107895304 | TTATTGTTTTATCAT[A/C]CCCCCAAAACTCATT | 11043 |
rs73251747 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107898571 | CTGGTCTTTAAATTA[C/T]AATTAGTTGTATTCA | 11043 |
rs73527019 | snp | A/G | 0.0379276 | 0.132383 | intron-variant | MID2 | GRCh38.p7 | X:107834234 | AGTAAGGCACAAGGT[A/G]AAGAAAAGCCATACA | 11043 |
rs73527020 | snp | A/G | 0.0338441 | 0.125605 | intron-variant | MID2 | GRCh38.p7 | X:107837299 | GTTATATAGTTTTCA[A/G]CATACATAGACATGG | 11043 |
rs73527024 | snp | A/T | 0.348932 | 0.229592 | intron-variant | MID2 | GRCh38.p7 | X:107839478 | CCAGGTTCAAGCGAT[A/T]CTTCTGGTTCAGCCT | 11043 |
rs73527030 | snp | A/G | 0.0560809 | 0.157783 | intron-variant | MID2 | GRCh38.p7 | X:107843813 | TGGAAAATCATTTAG[A/G]ATTACCCCCTTAGTC | 11043 |
rs73527036 | snp | C/T | 0.151636 | 0.229836 | intron-variant | MID2 | GRCh38.p7 | X:107854026 | TTCAATAATTACAGA[C/T]GGTCCCTGACTTACC | 11043 |
rs73527043 | snp | C/T | 0.151194 | 0.229646 | intron-variant | MID2 | GRCh38.p7 | X:107855882 | CCATAGAGTACTGGT[C/T]AAACTCAGATATGAG | 11043 |
rs73527047 | snp | A/C | 0.043513 | 0.140937 | intron-variant | MID2 | GRCh38.p7 | X:107858123 | GATTAAGATCACTAC[A/C]GATTTGTTAGCTGAC | 11043 |
rs73527061 | snp | A/G | 0.0440191 | 0.141675 | intron-variant | MID2 | GRCh38.p7 | X:107861987 | CATGTTAGCTGTGCA[A/G]CCTTGAACACATACT | 11043 |
rs73527066 | snp | A/T | 0.0440191 | 0.141675 | intron-variant | MID2 | GRCh38.p7 | X:107863141 | GAAAGTGCTTTATAA[A/T]TTTTCAGAGACCTAA | 11043 |
rs73529318 | snp | C/T | 0.0440191 | 0.141675 | intron-variant | MID2 | GRCh38.p7 | X:107863325 | TGTTTTCCTCGCCCT[C/T]CTCCCTCACATCTAT | 11043 |
rs73529321 | snp | C/T | 0.0440191 | 0.141675 | intron-variant | MID2 | GRCh38.p7 | X:107864086 | TCTCACTCCAAAGTC[C/T]ATGTTCTTTCCATTG | 11043 |
rs73529322 | snp | A/C/T | 0.5 | 0 | intron-variant | MID2 | GRCh38.p7 | X:107865131 | TTACTGAGGTCCTTG[A/C/T]TCTTAATGACTATGC | 11043 |
rs73529325 | snp | G/T | 0.0440191 | 0.141675 | intron-variant | MID2 | GRCh38.p7 | X:107865161 | CTGTATTAAAAAAGA[G/T]GGGCAAAACTAACAA | 11043 |
rs73529326 | snp | C/T | 0.0440191 | 0.141675 | intron-variant | MID2 | GRCh38.p7 | X:107865655 | TGCCTTTTGTTTTCT[C/T]TAATGAGAAACATTG | 11043 |
rs73529332 | snp | A/G | 0.0440191 | 0.141675 | intron-variant | MID2 | GRCh38.p7 | X:107865839 | CTAGTCGCATAGAAC[A/G]ACATAGTTCCATCCT | 11043 |
rs73529334 | snp | A/G | 0.0450304 | 0.143134 | intron-variant | MID2 | GRCh38.p7 | X:107867764 | TAAGAAAGAGAAGTT[A/G]AGAATGAAGCCCTGG | 11043 |
rs73529342 | snp | A/G | 0.0440191 | 0.141675 | intron-variant | MID2 | GRCh38.p7 | X:107871400 | GGTGCTGGCAGGAGC[A/G]AAACTGTGCTTCCCC | 11043 |
rs73529350 | snp | A/G | 0.0445249 | 0.142408 | intron-variant | MID2 | GRCh38.p7 | X:107871811 | CAACCATAGTCCCCA[A/G]TGTCCAGCTGCTTCT | 11043 |
rs73529352 | snp | A/G | 0.0440191 | 0.141675 | intron-variant | MID2 | GRCh38.p7 | X:107872320 | AGTTAAAAGGAGAGA[A/G]TCTAATGCTGAAGAT | 11043 |
rs73529353 | snp | C/T | 0.102711 | 0.202005 | intron-variant | MID2 | GRCh38.p7 | X:107875829 | ATTGGAGAGGAGAGC[C/T]GAGAGACCAACCCCA | 11043 |
rs73529358 | snp | C/T | 0.043513 | 0.140937 | intron-variant | MID2 | GRCh38.p7 | X:107875893 | ATTTTCAGAACTACC[C/T]GGGGCTCCTGGATGG | 11043 |
rs73529361 | snp | A/G | 0.0440191 | 0.141675 | intron-variant | MID2 | GRCh38.p7 | X:107878358 | CACTGCGTGCCATGC[A/G]TGTCTGCAGCTGTTG | 11043 |
rs73529364 | snp | A/G | 0.0297427 | 0.118265 | intron-variant | MID2 | GRCh38.p7 | X:107880682 | AACTCTGGAATAATG[A/G]CAGGTAATCATTTAT | 11043 |
rs73529370 | snp | G/T | 0.0440191 | 0.141675 | intron-variant | MID2 | GRCh38.p7 | X:107881831 | GTATAGAACAAGCAT[G/T]AGATGAATGATATTA | 11043 |
rs73531495 | snp | G/T | 0.0440191 | 0.141675 | intron-variant | MID2 | GRCh38.p7 | X:107884398 | GTCTCTGTTATCTCA[G/T]TTGATTCTCATAACC | 11043 |
rs73531498 | snp | C/T | 0.0440191 | 0.141675 | intron-variant | MID2 | GRCh38.p7 | X:107884614 | TTAGCACAGGAAAAT[C/T]CTCAAAAAAAGGGAA | 11043 |
rs73533405 | snp | G/T | 0.0440191 | 0.141675 | intron-variant | MID2 | GRCh38.p7 | X:107892382 | GCCTGTGCAAACCTC[G/T]ATTAGACTGCTTGCT | 11043 |
rs73533410 | snp | A/G | 0.0440191 | 0.141675 | intron-variant | MID2 | GRCh38.p7 | X:107892762 | TCTCATTCATTCCTT[A/G]AAAATATCACATCCT | 11043 |
rs73533411 | snp | C/G | 0.0440191 | 0.141675 | intron-variant | MID2 | GRCh38.p7 | X:107892785 | CACATCCTTAGGAAG[C/G]CTTCCTTGACCATCT | 11043 |
rs73533419 | snp | C/T | 0.0525796 | 0.153379 | intron-variant, nc-transcript-variant | MID2, LOC101928335 | GRCh38.p7 | X:107895480 | TGGCCCTGAGAGCCA[C/T]TGAATTTGTTGTGTA | 11043 |
rs73533422 | snp | A/G | 0.0440191 | 0.141675 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107896584 | ATTAGTTAGACATAG[A/G]GTAAAGTACATACAA | 11043 |
rs73533425 | snp | C/G | 0.0440191 | 0.141675 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107898022 | TCTGTTATGGAGTCT[C/G]AGAAGGTGGGATAGT | 11043 |
rs73533428 | snp | A/G | 0.0440191 | 0.141675 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107899457 | CTTACTCTACAGTCA[A/G]TCTTTGGGCTGGGAG | 11043 |
rs73533430 | snp | C/T | 0.0445249 | 0.142408 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107902071 | TGCACTCTCTCAGCC[C/T]AAATCTCATCCCTGC | 11043 |
rs73533431 | snp | C/T | 0.0440191 | 0.141675 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107902300 | CCAGGTACGACATCA[C/T]TGTGTACTACACCAG | 11043 |
rs73533434 | snp | A/G/T | 0.0440191 | 0.141675 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107903492 | TATATGTTTAATGAT[A/G/T]TATTTAATGTGAAAA | 11043 |
rs73533439 | snp | C/T | 0.0440191 | 0.141675 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107907257 | TGCTAACCTGAAATC[C/T]TTCTGCATTGCTTTG | 11043 |
rs73533443 | snp | C/T | 0.0440191 | 0.141675 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107907588 | ACTTCACATCCATTT[C/T]TAACCCACTCATGTC | 11043 |
rs73533446 | snp | C/G | 0.0440191 | 0.141675 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107909254 | TCTCCACTACTGAGG[C/G]AAAACCCTTCTGAGT | 11043 |
rs73533450 | snp | A/G | 0.0404706 | 0.136372 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107909534 | ACTCCAGCCAACTTC[A/G]TCCACTTGGATTCTC | 11043 |
rs73533453 | snp | A/G | 0.0440191 | 0.141675 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107910238 | ATTCCACCTATGTGC[A/G]AGATCATATGGTATT | 11043 |
rs73533458 | snp | C/T | 0.0404706 | 0.136372 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107914150 | TGTCTTTCTCCTTCA[C/T]GATGTGTGAGCTCTT | 11043 |
rs73533462 | snp | C/G | 0.0440191 | 0.141675 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107915673 | ACTGTTTTTACCAAA[C/G]CTTTAAAGGTCTAGT | 11043 |
rs73533464 | snp | C/T | 0.0440191 | 0.141675 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107916196 | GCTTTTACTTAAAAA[C/T]AATTTGAAAAAGACA | 11043 |
rs73533469 | snp | A/G | 0.0404706 | 0.136372 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107920708 | TACCTAGAGGATCAT[A/G]TATTTACCTTTTTAA | 11043 |
rs73533473 | snp | A/G | 0.0404706 | 0.136372 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107923611 | TTTGGTTATCATGTC[A/G]TCTCTTTGGCTTCCC | 11043 |
rs73533475 | snp | A/G | 0.0440191 | 0.141675 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107924583 | CCTGAGCAGGCACTC[A/G]CAGCAGTGCATGGGG | 11043 |
rs73533477 | snp | C/G | 0.0292288 | 0.117303 | utr-variant-3-prime, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107928325 | ATTCTCTTAGCCAAT[C/G]CCTCCACGCAAATGG | 11043 |
rs73533479 | snp | A/T | 0.0414859 | 0.13792 | utr-variant-3-prime, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107928414 | TATGATTTTTTTTTT[A/T]AAATTTCCATCGAAG | 11043 |
rs73636325 | snp | A/G | 0.00475684 | 0.0485365 | intron-variant | MID2 | GRCh38.p7 | X:107851552 | GCCCTGGGCTTTCCT[A/G]TTTCAGTCTGCCCCA | 11043 |
rs73636326 | snp | G/T | 0.0343555 | 0.126481 | intron-variant | MID2 | GRCh38.p7 | X:107854138 | TTACATCTGGATAAG[G/T]CCATCATAAGTTGAA | 11043 |
rs73636329 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107904193 | GGGAGAGGCAAAGAA[A/G]TGATGTTTGGCCTAC | 11043 |
rs73636330 | snp | A/G | 0.0157677 | 0.0873799 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107909087 | TTAATTTTCTCTTTC[A/G]GGATGCTGTATATTT | 11043 |
rs73636331 | snp | C/T | 0.0343555 | 0.126481 | utr-variant-3-prime, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107930293 | TTTGAGCTGTATTAA[C/T]TCTATTTTGCAGAGA | 11043 |
rs73636332 | snp | A/T | 0.0343555 | 0.126481 | downstream-variant-500B, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107931756 | ATATAATAGGTAGTG[A/T]TCTGGACAGAAAGGA | 11043 |
rs75045658 | snp | A/C | 0.5 | 0 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107925378 | TATAAAAATCTCTTG[A/C]CACACCCAGCAACTG | 11043 |
rs75055277 | snp | A/C | 0.000250944 | 0.0111986 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107926079 | TTCTTTTTTTTTTTT[A/C]TACTTATTTTTCAGG | 11043 |
rs76096211 | snp | A/T | 0 | 0 | intron-variant | MID2 | GRCh38.p7 | X:107867316 | CCGCCACGCCCAGCT[A/T]ATTTTTTTTTTTTTT | 11043 |
rs76835217 | snp | C/T | 0.5 | 0 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107911598 | CATTGTCTGGGTTTC[C/T]TCCCAGTTCCTTTTC | 11043 |
rs77132405 | snp | A/C | 0.5 | 0 | intron-variant | MID2 | GRCh38.p7 | X:107837597 | AAGATTTCCAGAATT[A/C]AAAAAAAAAAAAAAC | 11043 |
rs77178868 | snp | C/G | | | intron-variant | MID2 | GRCh38.p7 | X:107850189 | ATCCACACACACACA[C/G]ACACACACACACACA | 11043 |
rs78197354 | snp | C/G | 0.5 | 0 | intron-variant | MID2 | GRCh38.p7 | X:107890827 | AGCGAGGCTAGGGGA[C/G]GGGCGCCTGCCATTG | 11043 |
rs78889435 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | MID2 | GRCh38.p7 | X:107868832 | TTTAAGGGGGATCAA[C/T]CTATGCTTCCATGAT | 11043 |
rs79013847 | snp | C/G | | | intron-variant | MID2 | GRCh38.p7 | X:107850187 | ACATCCACACACACA[C/G]AGACACACACACACA | 11043 |
rs79700726 | snp | A/C | | | intron-variant, nc-transcript-variant | MID2, LOC101928335 | GRCh38.p7 | X:107895243 | GATAGTTCTATTAAT[A/C]TTATCACATTTATAG | 11043 |
rs79836794 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107890810 | GCCTACTCAAGCCTC[A/G]GCAATGGTGGGCGCC | 11043 |
rs80129037 | snp | A/T | 0 | 0 | intron-variant | MID2 | GRCh38.p7 | X:107867319 | CCACGCCCAGCTAAT[A/T]TTTTTTTTTTTTTTT | 11043 |
rs111246065 | snp | C/T | 0.0317957 | 0.122012 | intron-variant | MID2 | GRCh38.p7 | X:107838874 | CACTTTGGGAGGCTG[C/T]GGTGGGCAGATTGCT | 11043 |
rs111309619 | snp | C/T | 0 | 0 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107900505 | CAGCCTCCTAAATAG[C/T]CCTCAGGTTTACTAT | 11043 |
rs111325830 | snp | C/T | 0.111634 | 0.208218 | intron-variant | MID2 | GRCh38.p7 | X:107871527 | GTGTTAACAGCTCAG[C/T]GGAGGGTCAGTGTGA | 11043 |
rs111341791 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107916938 | CTGAAGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 11043 |
rs111401949 | snp | C/T | | | intron-variant | MID2 | GRCh38.p7 | X:107859220 | TTAAAATAAATTAAT[C/T]TAAAAAACACTGCTA | 11043 |
rs111455196 | snp | A/C | 0.5 | 0 | intron-variant | MID2 | GRCh38.p7 | X:107874366 | ATTATGTGGAGTGCA[A/C]ACAGTTAAGTTATTC | 11043 |
rs111527378 | snp | A/T | | | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107908295 | ATGCCACTTCCTTCC[A/T]CTCTATTCGGGATTC | 11043 |
rs111555513 | snp | G/T | | | intron-variant | MID2 | GRCh38.p7 | X:107829152 | GTGTTGGGATTACAG[G/T]TGTGAGCCACCACAC | 11043 |
rs111591969 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107865758 | ATCAAAGGCACAAAA[A/C]AATCACTGGCTTTGG | 11043 |
rs111603229 | in-del | -/CTT | 0 | 0 | intron-variant | MID2 | GRCh38.p7 | X:107835655 | CCATTTGTATATCTT[-/CTT]TGGAAAAAATCTATT | 11043 |
rs111634748 | snp | C/T | | | intron-variant | MID2 | GRCh38.p7 | X:107888859 | GTTGAATTGATCCCT[C/T]TACCATTATGTAATG | 11043 |
rs111645319 | snp | C/T | 0.103183 | 0.202348 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107913850 | TTCAGCATATTATTT[C/T]CCCACCTAATGCTTA | 11043 |
rs111684774 | snp | A/C | 0.5 | 0 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107926539 | CTCTAGTGATATCAG[A/C]ATTATGCATCTAAGT | 11043 |
rs111718118 | snp | A/G | | | intron-variant | MID2 | GRCh38.p7 | X:107885439 | ATCCATGTCCCTAAA[A/G]AGGACATGAACTCAT | 11043 |
rs111724867 | snp | C/T | 0 | 0 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107910835 | TTCCTTTCCTTTCCT[C/T]TCCCTCTCTCTTTCT | 11043 |
rs111756411 | snp | A/G | 0.103655 | 0.20269 | intron-variant | MID2 | GRCh38.p7 | X:107847113 | CATGAAGCTAGAACT[A/G]ACAATAACTTAAACC | 11043 |
rs111826064 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | MID2 | GRCh38.p7 | X:107825401 | TTTTTTGTAAAAAGA[A/G]AGAGAGGTTCGGTTT | 11043 |
rs111859615 | snp | C/T | 0.103655 | 0.20269 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107918113 | TATGGTGACAAGCCT[C/T]CTGCCTCTGTCACTC | 11043 |
rs111896973 | snp | A/G | 0 | 0 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107898873 | GGAGAGCACTGAGAC[A/G]GAGAAGCCAGTGAGG | 11043 |
rs111986573 | snp | C/T | 0.109764 | 0.206963 | intron-variant | MID2 | GRCh38.p7 | X:107862784 | ATTTAAAATGTTTAT[C/T]AGCAAAAATGTTCTG | 11043 |
rs111999486 | snp | C/G | | | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107915555 | ACAGCAAGACTCTGT[C/G]TCAAAAAAAAAAAAA | 11043 |
rs112058010 | snp | A/G | 0 | 0 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107926340 | TCTTTTCTGTCCTCT[A/G]TCATTAGGTTCCTAG | 11043 |
rs112104008 | snp | G/T | 0.0440191 | 0.141675 | intron-variant | MID2 | GRCh38.p7 | X:107877694 | CCAGGGCTTTATCTA[G/T]GCCGTGGAGCATGGC | 11043 |
rs112109809 | snp | A/T | 0.0168099 | 0.0901243 | upstream-variant-2KB, utr-variant-5-prime | MID2 | GRCh38.p7 | X:107824733 | AAGTTTTATGGTCCC[A/T]TTTACCTATTTTTGC | 11043 |
rs112292137 | snp | C/T | 0.0655152 | 0.168717 | intron-variant | MID2 | GRCh38.p7 | X:107838962 | AAATATAAACAAAAA[C/T]TAGCTGGGCTTGGTG | 11043 |
rs112362194 | snp | C/T | 0.0440191 | 0.141675 | intron-variant | MID2 | GRCh38.p7 | X:107871786 | AGTCAAGCTGCTTCT[C/T]TCCAACTTCCAACCA | 11043 |
rs112547188 | snp | C/T | 0 | 0 | intron-variant | MID2 | GRCh38.p7 | X:107842112 | GCAATAAATATTTTA[C/T]CCAGTATCAAATTTT | 11043 |
rs112588284 | snp | C/T | 0.0550819 | 0.156547 | intron-variant | MID2 | GRCh38.p7 | X:107854897 | TTTAAAAAGAATAGA[C/T]GGTGATGATGGACAG | 11043 |
rs112641024 | snp | A/G | | | intron-variant | MID2 | GRCh38.p7 | X:107826881 | GGGCGGTGCTGTCGC[A/G]GCAGCCGGCGTGGCT | 11043 |
rs112778829 | snp | A/T | 0.5 | 0 | missense, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107926949 | CATTTACAATCTGGA[A/T]CAAATCCCTAATGAT | 11043 |
rs112797714 | snp | A/G | 0 | 0 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107913878 | TTAGTGACCCCCATC[A/G]TTCTTAAGATAAAAT | 11043 |
rs112817732 | snp | C/T | 0.0440191 | 0.141675 | intron-variant | MID2 | GRCh38.p7 | X:107870060 | ATTTGAATGCTGTTT[C/T]ATTTAGAATTTTCAC | 11043 |
rs112848029 | snp | C/T | | | intron-variant | MID2 | GRCh38.p7 | X:107835778 | GATATAATAATATGA[C/T]TTGCAAATATTTGCG | 11043 |
rs112919920 | snp | A/C | 0.0068637 | 0.0581785 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107913076 | TACACACACACACAC[A/C]CCCCACCATGTCACT | 11043 |
rs112946380 | snp | C/T | 0.103655 | 0.20269 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107902322 | CTACACCAGTAGCCA[C/T]CTAAAAAAGAAATTA | 11043 |
rs113003496 | snp | A/G | | | intron-variant | MID2 | GRCh38.p7 | X:107874789 | CCCCTCAGTTGCTTG[A/G]GGGTTTTGGGGAGGG | 11043 |
rs113004465 | snp | C/T | 0.0440191 | 0.141675 | intron-variant | MID2 | GRCh38.p7 | X:107891429 | GAGATTACAGGCATG[C/T]GCCACCATGCCTGGC | 11043 |
rs113092379 | snp | C/T | 0.108827 | 0.206325 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107914603 | CAATGCCTTTTCTCT[C/T]TCCTCTAACCTACAT | 11043 |
rs113097340 | snp | A/G | 0.0440191 | 0.141675 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107916869 | AATGGGGCTGGGCAC[A/G]GTGGCTCACGCCCAT | 11043 |
rs113146370 | snp | C/T | 0.103655 | 0.20269 | intron-variant | MID2 | GRCh38.p7 | X:107869712 | AAGTACTTTGTACTC[C/T]TGTCCGTGCTGTGAA | 11043 |
rs113230272 | snp | A/G | 0.0440191 | 0.141675 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107914182 | AAGGCAAGAACCACA[A/G]CAAAGCTTGTTCACT | 11043 |
rs113246495 | snp | C/T | 0.0440191 | 0.141675 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107904229 | TGAATCCAGTAAAAA[C/T]GATGGCCATTCTGGG | 11043 |
rs113254019 | snp | A/G | 0.0240739 | 0.107039 | intron-variant | MID2 | GRCh38.p7 | X:107846700 | ATTTATTATTAACAG[A/G]ACCCTGTTTTGGAAG | 11043 |
rs113363470 | snp | A/G | 0.162169 | 0.234063 | utr-variant-5-prime | MID2 | GRCh38.p7 | X:107822804 | CCAGCTAATTTTTGT[A/G]TTTTTAGTAGAGATG | 11043 |
rs113364938 | snp | C/G | 0 | 0 | intron-variant | MID2 | GRCh38.p7 | X:107839665 | GTGAGCCACTGTGCC[C/G]GGCCGGGTGACCTCT | 11043 |
rs113382536 | snp | C/T | 0 | 0 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107924814 | TAATCTAGTAAAATC[C/T]TACTACAGAGAAGCC | 11043 |
rs113393851 | snp | A/G | 0.0440191 | 0.141675 | intron-variant | MID2 | GRCh38.p7 | X:107861468 | CTACAAAAAATACAA[A/G]AATTTGCCAGGTGTG | 11043 |
rs113398429 | snp | G/T | 0.102711 | 0.202005 | utr-variant-3-prime, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107927666 | ATTCACTTTATATAT[G/T]ACATATACACAAAAA | 11043 |
rs113527594 | snp | C/T | 0.0440191 | 0.141675 | intron-variant | MID2 | GRCh38.p7 | X:107880246 | GCAACCTCAGACTCC[C/T]GAGTAGCTGGGACTA | 11043 |
rs113615841 | snp | A/G | 0.0965482 | 0.197364 | intron-variant | MID2 | GRCh38.p7 | X:107850426 | TGAGAATAAATTCCA[A/G]TTTGAGAGGAGGCTT | 11043 |
rs113642863 | snp | A/G | | | intron-variant | MID2 | GRCh38.p7 | X:107832234 | CCCTGTGCAGGATGA[A/G]AGTTTAAGAGAAAAG | 11043 |
rs113647839 | snp | A/G | 0 | 0 | intron-variant | MID2 | GRCh38.p7 | X:107828367 | CCCAGGCTGGAGTGC[A/G]GTGTCACATTCACAG | 11043 |
rs113701835 | in-del | -/CTAA | 0.445616 | 0.155675 | intron-variant | MID2 | GRCh38.p7 | X:107844737 | ACCCCAGTGAGCCTC[-/CTAA]CTGTCTGCAAAATAT | 11043 |
rs113788033 | snp | C/G | 0 | 0 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107925181 | CTTTCCTAGAACTTT[C/G]CCCTGCTCTGTCTGA | 11043 |
rs113954023 | snp | A/G | 0 | 0 | utr-variant-3-prime, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107929644 | CTTTGCCTTGTCCTT[A/G]GCTCTCCAAAACTGT | 11043 |
rs114048258 | snp | A/G | | | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107908715 | AAAAAAAAAAAAAAA[A/G]CCTGCATCTGGTGAC | 11043 |
rs115737090 | snp | A/G | 0.0440191 | 0.141675 | intron-variant | MID2 | GRCh38.p7 | X:107869838 | ACCTTATATTTAAAA[A/G]AAAAACCTAGAGTCT | 11043 |
rs116408156 | snp | A/T | 0.0419931 | 0.138684 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107898916 | TATAATTATTATTAT[A/T]ATTATTGCATTTCAC | 11043 |
rs116625518 | snp | C/T | 0.0440191 | 0.141675 | intron-variant | MID2 | GRCh38.p7 | X:107879528 | TCTTCTCTCTGCTGG[C/T]GGAGCCTAGGTTTTT | 11043 |
rs137956768 | snp | A/T | 0.00581083 | 0.0535878 | intron-variant | MID2 | GRCh38.p7 | X:107858144 | GTTAGCTGACTTCTA[A/T]GGTAATGTAGCTTGT | 11043 |
rs138086734 | snp | C/G | 0.0282 | 0.115346 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107897627 | CATTTGAAACTTCCT[C/G]ATATAACAGGGCTAT | 11043 |
rs138137440 | snp | A/T | 0.0480577 | 0.147375 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107907887 | AATACCATTATCAAT[A/T]GAGTTCTTACTTTGT | 11043 |
rs138295131 | snp | A/G | 0.00896606 | 0.0663524 | intron-variant | MID2 | GRCh38.p7 | X:107881739 | AAAAACCAGTATTAA[A/G]TTCCTCTTCATAAAA | 11043 |
rs138338804 | snp | A/G | 0.0404706 | 0.136372 | intron-variant | MID2 | GRCh38.p7 | X:107876888 | CCTTACTGGGGTCAA[A/G]TTCACCAGGCATCTG | 11043 |
rs138403973 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | MID2 | GRCh38.p7 | X:107872290 | TCCTCTTTGGACATA[A/G]ATTTGGTCCATGCAT | 11043 |
rs138414570 | snp | A/C | | | intron-variant | MID2 | GRCh38.p7 | X:107847832 | TGAGATGGTGTGGTA[A/C]GTGCAATGACAGTGG | 11043 |
rs138452528 | snp | G/T | 0.0220041 | 0.102557 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107923760 | CCCCATGAACTGTGA[G/T]GTAGTAGAGAGAACA | 11043 |
rs138552159 | snp | C/T | 0.000140926 | 0.00839304 | missense, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107905620 | CTGCAAAAAATATTG[C/T]TGAGAGGTCAGTTCC | 11043 |
rs138637231 | snp | A/G | 0.000846024 | 0.0205498 | missense, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107926133 | AAATGACTCACAAGA[A/G]GTTGAAGATCTCCAA | 11043 |
rs138732818 | snp | A/T | 0.00896606 | 0.0663524 | intron-variant | MID2 | GRCh38.p7 | X:107893049 | TGGTAATATGAAATG[A/T]CCTGTAATGTATCCA | 11043 |
rs138743972 | snp | A/G | 0.00791544 | 0.0624105 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107923136 | ATTATAAGCCCTTTG[A/G]TCAGATCTCTTGCAA | 11043 |
rs138954278 | snp | C/G | 0.00422943 | 0.0457911 | intron-variant | MID2 | GRCh38.p7 | X:107846071 | TGAAGATGTGAGAGT[C/G]TGTAAATCTTCTGAT | 11043 |
rs138989088 | snp | C/T | 0.0147244 | 0.0845304 | intron-variant | MID2 | GRCh38.p7 | X:107891525 | CTCAAGTGATCTGCC[C/T]GCCTTAGCCTCCCAA | 11043 |
rs139022010 | snp | A/C | 0.0026455 | 0.0362733 | intron-variant | MID2 | GRCh38.p7 | X:107887306 | ACGTCCAATCAATGC[A/C]TAATTTCTTGAGAGT | 11043 |
rs139068959 | snp | A/G | 0.0399626 | 0.135589 | intron-variant | MID2 | GRCh38.p7 | X:107843333 | ACTAGCTATTTGAAA[A/G]CATCCGAAAACATGA | 11043 |
rs139091731 | snp | A/G | 0.00791544 | 0.0624105 | intron-variant | MID2 | GRCh38.p7 | X:107836129 | GAGTATTCTTTCTCC[A/G]TCGAATGGTCTTGGA | 11043 |
rs139130220 | snp | G/T | 0.00844089 | 0.0644143 | intron-variant | MID2 | GRCh38.p7 | X:107878747 | CTTTTACCCAAAAGA[G/T]AAATGGCAGGGTTGC | 11043 |
rs139130611 | snp | A/C | 0.0161584 | 0.0884199 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107926636 | TCAGATAATTCATAA[A/C]TGTTTATTTCTCTCT | 11043 |
rs139158123 | snp | A/C | 0.0068637 | 0.0581785 | intron-variant | MID2 | GRCh38.p7 | X:107830226 | ACAGGGACACAGAGC[A/C]CTTAAAAGGGTGAAG | 11043 |
rs139203816 | snp | C/T | 0.00896606 | 0.0663524 | intron-variant | MID2 | GRCh38.p7 | X:107859677 | GAGGAAACACTCAGG[C/T]CTGCCTGAGAAACTT | 11043 |
rs139220006 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | MID2 | GRCh38.p7 | X:107877315 | CTAAACCTTTGTGCT[A/G]TGAGGCATTTTACCT | 11043 |
rs139446213 | snp | A/G | 0.00633741 | 0.0559334 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107917225 | ATCACTTTAATGTCT[A/G]CATAAGTGTTTATGC | 11043 |
rs139448252 | snp | A/G | 0.0220041 | 0.102557 | intron-variant | MID2 | GRCh38.p7 | X:107832884 | AGGGGTTCTTTTCTA[A/G]TCATGGTGTTCTAGA | 11043 |
rs139491118 | snp | A/G | 0.00528398 | 0.051128 | intron-variant | MID2 | GRCh38.p7 | X:107864726 | ACAATGACTGCAAAT[A/G]TATAGATTTCCTCAA | 11043 |
rs139556503 | snp | A/G | 0.0110639 | 0.0735497 | intron-variant | MID2 | GRCh38.p7 | X:107860126 | ATTTTTACTGATCCA[A/G]GGAGAGATGAAGGCC | 11043 |
rs139586498 | snp | A/G | 0.0440191 | 0.141675 | intron-variant | MID2 | GRCh38.p7 | X:107883088 | CCATCATTCTCAGCA[A/G]GCTATCACAAGAACA | 11043 |
rs139624637 | snp | C/T | 0.0297427 | 0.118265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107898102 | GTCCCCCTCCCAGTT[C/T]TTCATGTACTGTGTC | 11043 |
rs139635650 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107848377 | TAGTACAGGTTTACT[A/T]TTAGAATGTCCAAAT | 11043 |
rs139659198 | snp | A/G | 0.00633741 | 0.0559334 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107900455 | TCCTTTCTATTACTG[A/G]TATTCTCCTTGGGTA | 11043 |
rs139700017 | snp | A/G | 0.022522 | 0.1037 | intron-variant | MID2 | GRCh38.p7 | X:107893286 | AAAAACACAGTCTTT[A/G]TCAGTGCTTCTTTTT | 11043 |
rs139705443 | snp | G/T | 0.00633741 | 0.0559334 | intron-variant | MID2 | GRCh38.p7 | X:107844905 | CAGGTCAGAAATAAT[G/T]TCTTGTATTTCTTTA | 11043 |
rs139770083 | snp | A/G | 0.018891 | 0.0953342 | intron-variant | MID2 | GRCh38.p7 | X:107890944 | ATAATCTGGTGTGCC[A/G]TTTGCTAAGACCATT | 11043 |
rs139826911 | snp | G/T | 0.000189982 | 0.00974449 | missense, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107926768 | TGCAATAGTAACTTC[G/T]TGGTGAGACACAACA | 11043 |
rs139896872 | snp | A/G | 0.0068637 | 0.0581785 | utr-variant-3-prime, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107927454 | GCCAGAGCGGGGGGT[A/G]GTCAGCCTTTCTAGT | 11043 |
rs139972539 | snp | A/C | 0.000189982 | 0.00974449 | synonymous-codon | MID2 | GRCh38.p7 | X:107841028 | CCCTAGTGAGAGCCG[A/C]CGGGAAAGGACTTAC | 11043 |
rs140057404 | snp | G/T | 0.0530806 | 0.154022 | intron-variant | MID2 | GRCh38.p7 | X:107869590 | CCTATCCAGAATCAC[G/T]GTATATCTTTGCATT | 11043 |
rs140077374 | snp | A/C | 0.00738971 | 0.0603345 | intron-variant, downstream-variant-500B | MID2, LOC101928335 | GRCh38.p7 | X:107894453 | GTGTTGTTATTCCAA[A/C]GTCTCTCCAAATCTT | 11043 |
rs140122398 | snp | C/T | 0.00633741 | 0.0559334 | intron-variant | MID2 | GRCh38.p7 | X:107865707 | TTTCCTCCTCTTCTC[C/T]ATATCCCAAGCCTGT | 11043 |
rs140185703 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107909642 | AGCTTTTCAAACAAA[C/T]GCTCCTGTAGTTTCT | 11043 |
rs140191060 | snp | A/G/T | 0.0105399 | 0.0718252 | intron-variant | MID2 | GRCh38.p7 | X:107867175 | GTTTTGTTTTGAGAC[A/G/T]GAGTCTCCCTTTGTC | 11043 |
rs140257861 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107913549 | GCATTATTGACTATA[G/T]GCATAAAAGCTCCTA | 11043 |
rs140292454 | snp | A/G | 0.0068637 | 0.0581785 | intron-variant | MID2 | GRCh38.p7 | X:107834086 | GGTGTGAGTCACCAC[A/G]CCAGACCCATTATTT | 11043 |
rs140324757 | snp | C/T | 0.0173306 | 0.0914601 | intron-variant | MID2 | GRCh38.p7 | X:107827938 | GATATTTATCCCTGC[C/T]CAAATCTTATGTACA | 11043 |
rs140426432 | snp | C/T | 0.00844089 | 0.0644143 | intron-variant | MID2 | GRCh38.p7 | X:107876505 | CTGAGAGGCTTAGTT[C/T]TGGTCCTACGTAAGC | 11043 |
rs140460790 | snp | A/G | 0.0214859 | 0.101397 | intron-variant | MID2 | GRCh38.p7 | X:107891342 | CTGGAATGCAGTGGC[A/G]CAATCTCAGCTCATT | 11043 |
rs140504946 | in-del | -/AGAG | | | intron-variant, nc-transcript-variant | MID2, LOC101928335 | GRCh38.p7 | X:107894867 | GTGTGTGTGTGTGAA[-/AGAG]AAGAGAGAGAGAGAG | 11043 |
rs140678314 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107846123 | TGAGTGTAAGGTAAG[A/C]TTTCTGTTGTCACCC | 11043 |
rs140735708 | snp | A/G | 0.000189982 | 0.00974449 | missense, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107905521 | AGGTTGCTAATTGCC[A/G]CCAGTGTCTTGAACG | 11043 |
rs140882306 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | MID2 | GRCh38.p7 | X:107829308 | ATCGTATCATTGTAC[A/G]TAGGTCCTAAATCTG | 11043 |
rs140910185 | snp | C/G | 0.0525796 | 0.153379 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107921859 | TACTTTCTGGCATAA[C/G]AAAATGTTCTAGGCT | 11043 |
rs140956023 | snp | A/G | 0.0530806 | 0.154022 | intron-variant | MID2 | GRCh38.p7 | X:107851476 | TTGGCCCAGACTTGC[A/G]TTACCCTACGGCCTT | 11043 |
rs141019855 | snp | G/T | 0.00317376 | 0.039709 | utr-variant-3-prime, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107930692 | CCTGGCAATGCCATG[G/T]ACCTTAAGAGAAGTA | 11043 |
rs141022185 | snp | G/T | 0.0530806 | 0.154022 | intron-variant | MID2 | GRCh38.p7 | X:107870222 | CTTTTGTTGCCCTGC[G/T]GCTTTTGTTAAACAT | 11043 |
rs141024135 | snp | C/T | 2.29708e-05 | 0.00338894 | missense | MID2 | GRCh38.p7 | X:107841171 | GTTGCCTGCGGGCCA[C/T]GCACCCCAACAAGAA | 11043 |
rs141039585 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107920655 | TACTTCCACTGACAT[A/G]ATTCAATCATAAGTC | 11043 |
rs141096806 | snp | A/C | 0.0384368 | 0.133195 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107901487 | TGAGTAACAAAGTGG[A/C]CATGTCTAATGAGGA | 11043 |
rs141105819 | snp | C/T | 0.0430067 | 0.140192 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107913926 | GCCTACAAAGTCCTG[C/T]ATGATTTTGTCTCAT | 11043 |
rs141148185 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107901931 | TGACTAATGAGAAAC[A/G]GATGACAGAATAAAG | 11043 |
rs141361786 | snp | A/G | 0.127347 | 0.217844 | intron-variant | MID2 | GRCh38.p7 | X:107886945 | TTATTGGTGTATAAG[A/G]ATGCTTGTGATTTTT | 11043 |
rs141441758 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107840255 | TCACATAGAAGCAGC[C/T]CTACAGTTTACCTTG | 11043 |
rs141483499 | snp | A/G | | | intron-variant | MID2 | GRCh38.p7 | X:107887335 | GTTTTTAGCATGAAG[A/G]GTTGTTGAATTTTGT | 11043 |
rs141499771 | snp | C/T | 0.0220041 | 0.102557 | intron-variant | MID2 | GRCh38.p7 | X:107881477 | ACTCTCTTTGTTCTG[C/T]CCAGTGATGACCTTT | 11043 |
rs141508430 | snp | C/T | 0.0763124 | 0.179813 | intron-variant | MID2 | GRCh38.p7 | X:107845451 | GATCTTGTTATAAAA[C/T]ATTACCCAGCACTGG | 11043 |
rs141574483 | snp | A/G | 0.00377333 | 0.0432715 | intron-variant | MID2 | GRCh38.p7 | X:107841402 | TAAGGGATCTGGGGA[A/G]CATCCCCTATACAAC | 11043 |
rs141602275 | snp | A/G | 0.0110639 | 0.0735497 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107925764 | TTGATAATATATGAT[A/G]TGGGGGACAGCTTAT | 11043 |
rs141743917 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107897902 | TGTTCATAATAATTT[A/C]TTGATAATTCATCAG | 11043 |
rs141886458 | snp | C/T | 0.00158814 | 0.0281345 | utr-variant-5-prime | MID2 | GRCh38.p7 | X:107823326 | GCTTCTGTATGCGAA[C/T]AGTAGGAAATCATAC | 11043 |
rs141906917 | snp | A/T | 0.00317376 | 0.039709 | intron-variant | MID2 | GRCh38.p7 | X:107859900 | GTATGGAGAAGTGAG[A/T]AGCTTGGGCCCAAAT | 11043 |
rs141910857 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107908102 | TAGTGCCACAGTCTA[C/T]ACTTTTACAACAAAG | 11043 |
rs141923491 | snp | A/G | 0.01368 | 0.0815649 | intron-variant | MID2 | GRCh38.p7 | X:107841900 | TATGTTTGTGTTTGT[A/G]TACTCAATACACTAA | 11043 |
rs141974804 | snp | A/G | 0.0297427 | 0.118265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107904132 | CAAAGTTTGATCCAG[A/G]TGATTCTGGTTTGAT | 11043 |
rs142033425 | snp | A/T | 0.0369084 | 0.130736 | intron-variant | MID2 | GRCh38.p7 | X:107878062 | CCCCTTGCTCTATGC[A/T]AATGGGTTCCTTTAA | 11043 |
rs142101113 | snp | C/T | 0.00844089 | 0.0644143 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107911396 | CTTATTTTACTAAGA[C/T]ACTTCCTTAATTTTT | 11043 |
rs142141822 | snp | A/G | 0.0465453 | 0.14528 | intron-variant | MID2 | GRCh38.p7 | X:107843873 | GAAAGTTGGCTGGCA[A/G]GAGCTATGGGAGAGT | 11043 |
rs142238509 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | MID2 | GRCh38.p7 | X:107842649 | GTAGTCACAATGACT[A/G]TGGTTTGTGCCTCTT | 11043 |
rs142246244 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | MID2 | GRCh38.p7 | X:107850590 | TTCAAAGCATTTTCA[C/T]ATTAATGAAGTAAGG | 11043 |
rs142324031 | snp | C/T | 0.0100156 | 0.0700533 | intron-variant | MID2 | GRCh38.p7 | X:107835421 | CTTTTGAGGAACTGT[C/T]GAACTATTTCCCAAA | 11043 |
rs142356828 | snp | A/G | 0.00896606 | 0.0663524 | intron-variant | MID2 | GRCh38.p7 | X:107880921 | CGTTTTCTCACTGTT[A/G]TAAGTTTTGCAAAGG | 11043 |
rs142409512 | snp | A/G | 0.0220041 | 0.102557 | intron-variant | MID2 | GRCh38.p7 | X:107861743 | AAGTCAGACTCATAA[A/G]TGCTCTGTTTGTGTA | 11043 |
rs142586742 | snp | A/G | 0.0399626 | 0.135589 | intron-variant | MID2 | GRCh38.p7 | X:107883013 | ACACCGTGGAATACT[A/G]TGCAGCCATAAAAAA | 11043 |
rs142653480 | snp | C/G | 0.0220041 | 0.102557 | intron-variant | MID2 | GRCh38.p7 | X:107864136 | GAAGTTGTTGGTTTA[C/G]TTGCCACCGATTCAT | 11043 |
rs142717164 | snp | A/G | 0.00844089 | 0.0644143 | intron-variant | MID2 | GRCh38.p7 | X:107868125 | TTTTGTGGCATATAC[A/G]TTATATATCAATAAA | 11043 |
rs142724460 | snp | A/G | 0.0110639 | 0.0735497 | utr-variant-3-prime, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107929246 | TCTCCTTCATTTCTC[A/G]GTCACCTTTGTCTCT | 11043 |
rs142743890 | snp | G/T | 0.00317376 | 0.039709 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107897215 | TCTAGAAATGGCTTG[G/T]CTGCCACCTCCCCAT | 11043 |
rs142785749 | snp | C/G | 0.00370173 | 0.0428621 | intron-variant | MID2 | GRCh38.p7 | X:107865111 | TTAAGAGTTTGCATC[C/G]AATTTTACTGAGGTC | 11043 |
rs142927690 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107901105 | TGATAAGGGCTTCAA[C/T]CTATTGGTTCCTTGG | 11043 |
rs142967797 | snp | A/C | 0.00475684 | 0.0485365 | intron-variant | MID2 | GRCh38.p7 | X:107831355 | AATCTGATAACAAAC[A/C]CATCATACAATCTGA | 11043 |
rs143091681 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107923189 | CAATTTTCAACCTCA[C/G]TAAATTTTGTACTAG | 11043 |
rs143128992 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107902701 | GACAGGTATTTTGCT[C/T]GGGTTGGAGAATATG | 11043 |
rs143183058 | snp | A/G | 0.0173306 | 0.0914601 | intron-variant | MID2 | GRCh38.p7 | X:107833201 | GGTAACAGATAGCAA[A/G]AGCTCTATAATAATC | 11043 |
rs143248182 | snp | A/G | 0.00738971 | 0.0603345 | intron-variant | MID2 | GRCh38.p7 | X:107878625 | GGGTCCAGTTCAGGG[A/G]CCTTCTGGCAACAAC | 11043 |
rs143268085 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107914191 | ACCACAGCAAAGCTT[C/G]TTCACTTTGTGTATC | 11043 |
rs143415131 | in-del | -/CTT | | | intron-variant | MID2 | GRCh38.p7 | X:107835656 | GGCCATTTGTATATC[-/CTT]TTTGGAAAAAATCTA | 11043 |
rs143517468 | snp | C/T | 0.00633741 | 0.0559334 | intron-variant | MID2 | GRCh38.p7 | X:107858222 | AAATGTTTTCTGCTG[C/T]GGCTGGAGAGCATGG | 11043 |
rs143552092 | snp | A/C | 0.0245906 | 0.108123 | intron-variant | MID2 | GRCh38.p7 | X:107863978 | CAGCTGGTTAATATT[A/C]CCATTTTTCAAGTGA | 11043 |
rs143695799 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107841614 | TGGGGAGTCAGCTCA[A/T]GGCCTGCAACACCAG | 11043 |
rs143729032 | snp | G/T | 0.00844089 | 0.0644143 | intron-variant | MID2 | GRCh38.p7 | X:107885019 | AGCAGTAACAATGTA[G/T]TAAGATGGCCAGATT | 11043 |
rs143742928 | snp | A/C | 0.00896606 | 0.0663524 | intron-variant, nc-transcript-variant | MID2, LOC101928335 | GRCh38.p7 | X:107894912 | AGCAAAGGCCTGAAG[A/C]TATATTAGAACTTCA | 11043 |
rs143835851 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | MID2 | GRCh38.p7 | X:107892670 | TCTGGCCCCTACCTA[C/T]CTCTCTAGCATGGTC | 11043 |
rs143871680 | snp | A/T | | | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107910598 | TTTTATAATGGCTGT[A/T]CTAATTTATATTCCC | 11043 |
rs143907996 | snp | A/C | 0.00475684 | 0.0485365 | intron-variant | MID2 | GRCh38.p7 | X:107877149 | ACTATCAGCAAAGGT[A/C]TGGATTACTTGCAAG | 11043 |
rs143923920 | snp | C/T | 0.0173306 | 0.0914601 | intron-variant | MID2 | GRCh38.p7 | X:107843612 | CTGTGTGGTTCGTTA[C/T]GTTGTCTGAAACATC | 11043 |
rs144066298 | snp | A/G | 0.0525796 | 0.153379 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107918370 | GGTGAGGGATGGTGG[A/G]AATGGAAACAAAAGC | 11043 |
rs144108832 | snp | A/G | 2.27886e-05 | 0.00337547 | missense | MID2 | GRCh38.p7 | X:107840840 | GCCCATCGCATTTTG[A/G]TATCAAGCTGCAGCT | 11043 |
rs144167265 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | MID2 | GRCh38.p7 | X:107893556 | ACTTTTAAAAAGGAA[C/T]GATTAAGTAGATATA | 11043 |
rs144208093 | snp | C/T | 0.0220041 | 0.102557 | intron-variant | MID2 | GRCh38.p7 | X:107866070 | CACGATGCCAGTTTA[C/T]TCTATAGTGCACATA | 11043 |
rs144270984 | snp | C/T | 4.60968e-05 | 0.00480065 | missense, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107927008 | ATTGATTACCCTGAG[C/T]GGCAGGAATGCAACT | 11043 |
rs144333492 | snp | C/T | 0.00844089 | 0.0644143 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107905880 | TTGCTGCTCACTCAG[C/T]GCATGAGTTTTCTAT | 11043 |
rs144343570 | snp | A/G | 0.0550819 | 0.156547 | intron-variant | MID2 | GRCh38.p7 | X:107855696 | GAGAATCTTCTTGTA[A/G]GGCAAAGAATCCTCT | 11043 |
rs144370342 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107924695 | GTGGACTCAGAGATA[C/T]GCACAAAAAGACTGT | 11043 |
rs144372492 | snp | A/G | 0.00738971 | 0.0603345 | intron-variant | MID2 | GRCh38.p7 | X:107837555 | AAAAAAAAAAACTCT[A/G]TAAACTATGTTAAAT | 11043 |
rs144425647 | snp | A/C | 0.0645269 | 0.16763 | intron-variant | MID2 | GRCh38.p7 | X:107889606 | TGTGTCTTGGAGTTG[A/C]TCTTCTCGAGGGTAT | 11043 |
rs144492053 | snp | A/G | 0.0399626 | 0.135589 | intron-variant | MID2 | GRCh38.p7 | X:107883233 | GAAGGGTTAGCATGA[A/G]GAGAAATGCCTAATG | 11043 |
rs144598021 | snp | A/G | 2.27892e-05 | 0.00337551 | missense | MID2 | GRCh38.p7 | X:107840912 | ACCTGCAGGTATGTT[A/G]TCTCGCTGAACCACC | 11043 |
rs144599643 | snp | A/G | 9.13378e-05 | 0.00675726 | missense, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107905544 | CTTGAACGGTCAACA[A/G]TCCTCATCAACCAAG | 11043 |
rs144898177 | snp | C/T | 0.0282 | 0.115346 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107906201 | AAAAAAACCAGGGTC[C/T]AAAGTGAAACATTGT | 11043 |
rs144918770 | snp | A/G | 0.0525796 | 0.153379 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107914019 | TTACTCATTACATAG[A/G]TCATTGGTGAAAATC | 11043 |
rs144994570 | snp | A/G | 0.00949095 | 0.0682305 | intron-variant | MID2 | GRCh38.p7 | X:107834554 | TTTAATTTTTGTCAT[A/G]CCACTTCCTCCTGCT | 11043 |
rs145029716 | snp | A/G | 0.0535814 | 0.15466 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107906866 | GTTGGGATTACAGGC[A/G]TGAGCCACTGCCCTC | 11043 |
rs145111927 | snp | C/T | 0.00896606 | 0.0663524 | intron-variant | MID2 | GRCh38.p7 | X:107891505 | AGGCTGAGCCTAAAA[C/T]AGACCTCAAGTGATC | 11043 |
rs145144797 | snp | C/T | | | intron-variant | MID2 | GRCh38.p7 | X:107887300 | TGAGATACGTCCAAT[C/T]AATGCCTAATTTCTT | 11043 |
rs145224159 | snp | C/G | 0.0068637 | 0.0581785 | intron-variant | MID2 | GRCh38.p7 | X:107845876 | TCTCAACCAGTGTAA[C/G]TATAAATATAAGGGA | 11043 |
rs145252587 | snp | C/T | 0.0110639 | 0.0735497 | intron-variant | MID2 | GRCh38.p7 | X:107849348 | GACAAATGGAGATCA[C/T]GGTCCAGTTTGTGCC | 11043 |
rs145257502 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | MID2 | GRCh38.p7 | X:107891424 | TAGCTGAGATTACAG[A/G]CATGCGCCACCATGC | 11043 |
rs145285321 | snp | C/G | 0.0348667 | 0.127349 | intron-variant | MID2 | GRCh38.p7 | X:107845024 | CAGTGCCTATAGCTT[C/G]CTTTGGATCTCATCT | 11043 |
rs145307560 | snp | A/G | 2.2969e-05 | 0.0033888 | missense, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107917727 | TGCTCAAGATTGGCC[A/G]GGGCGCCACGAGGCA | 11043 |
rs145359982 | snp | C/G/T | 9.18885e-05 | 0.0067776 | missense, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107927002 | GATTTTATTGATTAC[C/G/T]CTGAGCGGCAGGAAT | 11043 |
rs145397838 | snp | C/G | 0.00013796 | 0.00830426 | missense | MID2 | GRCh38.p7 | X:107841155 | GTCTCCTACTGTGAC[C/G]GTTGCCTGCGGGCCA | 11043 |
rs145454649 | snp | C/T | 0.0530806 | 0.154022 | intron-variant | MID2 | GRCh38.p7 | X:107871023 | TCATTTTTTTGTCCT[C/T]TTCCAGTTTCTTAAA | 11043 |
rs145488866 | snp | A/C | 0.022522 | 0.1037 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107917450 | AGAGTAACAATTGTA[A/C]AATTCCAGAAGAGAA | 11043 |
rs145517137 | snp | A/G | | | intron-variant | MID2 | GRCh38.p7 | X:107828496 | TTTGTATTTTTTGTA[A/G]AGATGGCGTTTTGCC | 11043 |
rs145525507 | snp | A/G | 0.022522 | 0.1037 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107907831 | ATAAGTCATATTGCA[A/G]GAAATAGCAATCTCC | 11043 |
rs145702239 | snp | A/G | 0.00633741 | 0.0559334 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107909800 | TTATTGTGTTGAGAC[A/G]TTCACTGCCGTTTTG | 11043 |
rs145853577 | snp | C/T | 0.00025875 | 0.0113714 | synonymous-codon, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107904041 | GAGGAAGCAAATGAT[C/T]GCTGTCAAAATCAAA | 11043 |
rs145869208 | snp | A/G | | | intron-variant | MID2 | GRCh38.p7 | X:107846187 | TGAGGCTAAGGATCA[A/G]TCTAATAAATGAGCC | 11043 |
rs145874733 | snp | A/G | 0.104598 | 0.203367 | intron-variant | MID2 | GRCh38.p7 | X:107857784 | TCATGAAAGTAAGAC[A/G]CTGATGGGTGATTTG | 11043 |
rs145901150 | snp | C/T | 0.00738971 | 0.0603345 | intron-variant | MID2 | GRCh38.p7 | X:107858399 | CCTCTGTATAATGCA[C/T]AGCCAAGGGAAAATG | 11043 |
rs145976139 | snp | G/T | 0.0220041 | 0.102557 | utr-variant-3-prime, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107927287 | CTGAGTAGTCTGCGT[G/T]CAAGCCATTGGAGAA | 11043 |
rs146040185 | snp | A/G | 0.0131573 | 0.0800346 | intron-variant | MID2 | GRCh38.p7 | X:107864714 | AAATATAATACCACA[A/G]TGACTGCAAATATAT | 11043 |
rs146058302 | snp | C/T | 0.0194105 | 0.0965841 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107898396 | GCCTAAACTTGTCTC[C/T]CCTTAAGCTCCATTT | 11043 |
rs146201586 | snp | A/G | 0.0068637 | 0.0581785 | intron-variant | MID2 | GRCh38.p7 | X:107882815 | CTTCAAGGATCTGGA[A/G]CTAGAAATACAATTT | 11043 |
rs146238646 | snp | A/G | 0.0409784 | 0.137149 | intron-variant | MID2 | GRCh38.p7 | X:107880360 | TTCCTAGGCTCAAGC[A/G]ATCTGCCCACTTCAG | 11043 |
rs146301130 | snp | C/T | 0.0525796 | 0.153379 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107908553 | TCATCTCTAGTTTGA[C/T]TTGGGTCTTTTAAAA | 11043 |
rs146376786 | snp | C/T | 0.00738971 | 0.0603345 | intron-variant | MID2 | GRCh38.p7 | X:107835518 | TGACGTGCTGTTTTC[C/T]GGTTTTTGTTTGTTT | 11043 |
rs146481924 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107920334 | CACCTCTTCTAAGAT[C/T]TGAAATGATCACAAC | 11043 |
rs146500604 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107913907 | ATCCAACGTTTGTAA[C/T]GTGGCCTACAAAGTC | 11043 |
rs146604322 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | MID2 | GRCh38.p7 | X:107857183 | TTAGGATTCTGTCTT[C/T]GATGACAGGGACCCT | 11043 |
rs146616495 | snp | G/T | 0.00896606 | 0.0663524 | intron-variant | MID2 | GRCh38.p7 | X:107877178 | AGGAAAAGAAAGTCT[G/T]CATGTATGGCCTCAG | 11043 |
rs146683713 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | MID2 | GRCh38.p7 | X:107833577 | ATGCTTTGCAGACCC[A/G]GAAGAAAAAAAATTA | 11043 |
rs146701604 | snp | A/T | 0.0874553 | 0.189945 | intron-variant | MID2 | GRCh38.p7 | X:107827792 | CTCTCATGACTGTAC[A/T]GAGGGAGAAACTGTC | 11043 |
rs146702010 | snp | C/T | 0.016289 | 0.0887646 | intron-variant | MID2 | GRCh38.p7 | X:107878640 | GCCTTCTGGCAACAA[C/T]GAGGAGTGGCATTGG | 11043 |
rs146803923 | snp | A/G | 0.00791544 | 0.0624105 | intron-variant | MID2 | GRCh38.p7 | X:107854999 | AAGTGTGCTTCATCC[A/G]TCATCAAACTGGACA | 11043 |
rs146822824 | snp | A/G | 0.0100156 | 0.0700533 | intron-variant | MID2 | GRCh38.p7 | X:107851707 | ACAAAGAAACTACAA[A/G]CTCCTTATCTAGGCA | 11043 |
rs146964879 | snp | A/T | 0.0379276 | 0.132383 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107897319 | GGCCAAAAAAATTAC[A/T]CACTGAAGCTGTAGA | 11043 |
rs147036340 | snp | A/G | 0.017851 | 0.0927731 | intron-variant | MID2 | GRCh38.p7 | X:107876719 | CTTCTCAGTGTTAGG[A/G]TTTGATTCAAAAGTA | 11043 |
rs147125268 | snp | G/T | 0.00317376 | 0.039709 | intron-variant | MID2 | GRCh38.p7 | X:107862020 | TTCTGAGCCTCAGTT[G/T]CACCATCTATAAAAC | 11043 |
rs147208317 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | MID2 | GRCh38.p7 | X:107849414 | TGGTGTCTTGATGTA[C/T]GCCTAGTTTTCTTGA | 11043 |
rs147263809 | snp | A/G | 0.00738971 | 0.0603345 | intron-variant | MID2 | GRCh38.p7 | X:107829888 | CTTTATGAACATATC[A/G]TCTGAATGGTGCAAA | 11043 |
rs147280961 | snp | A/G | 0.00791544 | 0.0624105 | utr-variant-5-prime | MID2 | GRCh38.p7 | X:107823492 | TATCAGGCTGGATTC[A/G]GCAGACTTCTGACTC | 11043 |
rs147297510 | snp | C/T | 0.00633741 | 0.0559334 | intron-variant | MID2 | GRCh38.p7 | X:107872611 | TACAATGATCTATTC[C/T]AGTGACTTTCAGTGC | 11043 |
rs147387343 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | MID2 | GRCh38.p7 | X:107848323 | GGCTTTGGCTCACTA[A/G]TCTGAGGGTTATCAA | 11043 |
rs147420346 | snp | A/G | 0.103655 | 0.20269 | intron-variant | MID2 | GRCh38.p7 | X:107889738 | GGTTCCATTCTCCCC[A/G]TCACTTTCAGGTACA | 11043 |
rs147431248 | snp | C/T | 4.56314e-05 | 0.00477636 | synonymous-codon, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107926230 | TGGCACAGGGTGCTA[C/T]GGGGCAGCAGGAAAT | 11043 |
rs147523777 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107909580 | ATTTTAGGGAACTCA[C/T]TGGGCTCTGCCTGGA | 11043 |
rs147558772 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107862376 | AATTTCAAATTTTAC[A/G]TATATCAACTAAAAC | 11043 |
rs147574191 | snp | C/T | 0.0214859 | 0.101397 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107907037 | ATTTCTCACTTCAGA[C/T]ACTCTCTTTTCAATA | 11043 |
rs147765700 | snp | C/T | 0.00475684 | 0.0485365 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107901864 | AATCTCGGGCAAAGG[C/T]ACAGGACATGAAAGT | 11043 |
rs147855721 | snp | A/C | 0.0768 | 0.180282 | intron-variant | MID2 | GRCh38.p7 | X:107883385 | GAAAAAGGAGGGAAT[A/C]GATCAAACAAGTATA | 11043 |
rs147870151 | snp | A/G | | | utr-variant-3-prime, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107929471 | TTTAACTATTTACAC[A/G]ACTATTCACACAAGT | 11043 |
rs147886536 | snp | A/G/T | 0.000137179 | 0.00828085 | missense | MID2 | GRCh38.p7 | X:107841027 | CCCCTAGTGAGAGCC[A/G/T]CCGGGAAAGGACTTA | 11043 |
rs148012020 | snp | G/T | 0.000189982 | 0.00974449 | missense, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107917730 | TCAAGATTGGCCGGG[G/T]CGCCACGAGGCAAGT | 11043 |
rs148097924 | snp | A/G | 0.0302564 | 0.119217 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107908682 | CAGCCTGGGCAACAT[A/G]GCGAGATTCCATCTA | 11043 |
rs148117734 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | MID2 | GRCh38.p7 | X:107841769 | TTAGCATATGTGTCG[A/G]TTTGCATATGTAGGT | 11043 |
rs148134633 | snp | C/T | 0.313263 | 0.241863 | intron-variant | MID2 | GRCh38.p7 | X:107886559 | cgtcaggtagcgtga[C/T]gcttccagctttatt | 11043 |
rs148189184 | snp | C/G | 0.0282 | 0.115346 | intron-variant | MID2 | GRCh38.p7 | X:107853931 | CCCATTTGTAAAATA[C/G]TAGCATCTTCTACTT | 11043 |
rs148256675 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107902910 | GACTGCTCTGTGTGC[G/T]GCTGAAATGGAACTG | 11043 |
rs148328934 | snp | C/T | | | intron-variant | MID2 | GRCh38.p7 | X:107881251 | CCACTGGGTTAGGGT[C/T]AGGTCTGACAAAATT | 11043 |
rs148499473 | snp | C/T | | | intron-variant | MID2 | GRCh38.p7 | X:107893742 | ATAAGCTGCGTACAC[C/T]GAACCTCATTTTATT | 11043 |
rs148588143 | snp | A/G | 0.00475684 | 0.0485365 | intron-variant | MID2 | GRCh38.p7 | X:107877772 | ATTTATACTGTGCCT[A/G]TTGCCTCACTTGGGA | 11043 |
rs148761455 | snp | C/T | 0.0530806 | 0.154022 | intron-variant | MID2 | GRCh38.p7 | X:107861472 | AAAAAATACAAAAAT[C/T]TGCCAGGTGTGGTGG | 11043 |
rs148778025 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107905895 | CGCATGAGTTTTCTA[C/T]GATGGTGTTGGTATA | 11043 |
rs148800509 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107838227 | GCACAACAAGTTCAT[G/T]TATAGACATGTTGAG | 11043 |
rs148813245 | snp | A/C | 0.00844089 | 0.0644143 | intron-variant | MID2 | GRCh38.p7 | X:107858104 | CTATTATAACAGAAA[A/C]AGAGATTAAGATCAC | 11043 |
rs148883229 | snp | A/G | 0.00896606 | 0.0663524 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107907595 | ATCCATTTTTAACCC[A/G]CTCATGTCTTTCCTA | 11043 |
rs148900032 | snp | A/C | 0.0515767 | 0.15208 | utr-variant-3-prime, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107928744 | TGGAAGAAACAAAGT[A/C]TATAATCCTCCCCAA | 11043 |
rs149022058 | snp | C/T | 0.0425 | 0.139441 | intron-variant, nc-transcript-variant | MID2, LOC101928335 | GRCh38.p7 | X:107896238 | ATAGTCCCAGCTACT[C/T]GGCGGGGTTGGGGGG | 11043 |
rs149042249 | snp | A/G | 0.0399626 | 0.135589 | intron-variant | MID2 | GRCh38.p7 | X:107826763 | TCGAGCGAATCCCCC[A/G]GCGCCTGGGCGCGAG | 11043 |
rs149268554 | snp | C/T | 0.0105399 | 0.0718252 | intron-variant | MID2 | GRCh38.p7 | X:107847912 | GGGTGAGTTTTTGAA[C/T]GCCCTGTTAGGGGAC | 11043 |
rs149286259 | snp | A/C | 0.0126344 | 0.0784702 | intron-variant | MID2 | GRCh38.p7 | X:107863560 | GGCTCCTCTTGTTTG[A/C]TCCACTATTTTCACA | 11043 |
rs149340303 | snp | A/G | 0.0220041 | 0.102557 | utr-variant-5-prime | MID2 | GRCh38.p7 | X:107822691 | CTGGAATGCAGCGGC[A/G]CGATCTTGGCTCACT | 11043 |
rs149356874 | snp | C/T | 0.0530806 | 0.154022 | intron-variant | MID2 | GRCh38.p7 | X:107872020 | CTGCCCAGAATTTCC[C/T]TGCCTCCTGCCCCTG | 11043 |
rs149409547 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107877497 | GTATGAGGGAGAGAG[A/G]AAGTGAACCTCCTCC | 11043 |
rs149479227 | snp | A/G | 0.0440191 | 0.141675 | intron-variant | MID2 | GRCh38.p7 | X:107888528 | TTTACATTTGCTGAG[A/G]AGTGCTTTACTGTGG | 11043 |
rs149669553 | snp | C/G | 0.00896606 | 0.0663524 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107917423 | CTTCAAGAGATGTTG[C/G]GTTACGCAGGAAGAG | 11043 |
rs149722664 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | MID2 | GRCh38.p7 | X:107839887 | CACAAGGCAATATGA[C/T]TTTATTATTGATCAG | 11043 |
rs149830662 | snp | C/T | 0.000160223 | 0.00894908 | synonymous-codon | MID2 | GRCh38.p7 | X:107854653 | GGTTAAGCGCAACAG[C/T]GAACTAGAAAATCAA | 11043 |
rs149863795 | snp | A/G | 0.00896606 | 0.0663524 | intron-variant | MID2 | GRCh38.p7 | X:107870519 | TATTAGATTCTTGAG[A/G]TTTTGTTACTCCTTC | 11043 |
rs149882308 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | MID2 | GRCh38.p7 | X:107873788 | ACTGCCACTTCACAT[A/G]TGAGAAAAACCGAGG | 11043 |
rs149934189 | snp | A/G | 0.00633741 | 0.0559334 | intron-variant | MID2 | GRCh38.p7 | X:107879107 | GCAGCAGCATCTGGC[A/G]GGGGTGGGGCCATGA | 11043 |
rs149985983 | snp | A/C | 0.00896606 | 0.0663524 | intron-variant | MID2 | GRCh38.p7 | X:107845457 | GTTATAAAATATTAC[A/C]CAGCACTGGAGTAAG | 11043 |
rs150002621 | snp | C/T | | | intron-variant | MID2 | GRCh38.p7 | X:107891405 | CCTGCCTCAGACTCC[C/T]GAGTAGCTGAGATTA | 11043 |
rs150022207 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107904406 | AGTCAGGATTATGGA[C/T]CATGAATTCCAGGAT | 11043 |
rs150104874 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107892868 | AGATTATCCTTTTTA[C/T]GTGATAAACCTCTTT | 11043 |
rs150122493 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107907566 | AATTTATCCCTCTCT[A/G]TAGTTGACTTCACAT | 11043 |
rs150177221 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107829508 | TGGGGGCAGTTTGTT[A/G]GCTTCTAATGAAAAG | 11043 |
rs150192041 | snp | A/G | 0.0333324 | 0.12472 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107923054 | CTCTTTCTCCTGCAT[A/G]TCTGTTTGCCCTCCA | 11043 |
rs150246654 | snp | A/T | 0.00581083 | 0.0535878 | intron-variant | MID2 | GRCh38.p7 | X:107842310 | TTACACTGATGATCC[A/T]GCGAATTGTTTTATT | 11043 |
rs150265191 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | MID2 | GRCh38.p7 | X:107857441 | ACACGCCACCATGCC[C/T]GCCTAATTTCTTGTA | 11043 |
rs150281697 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107901550 | TCCAACAAATAATTA[C/T]GGAGCATCTACTATG | 11043 |
rs150334097 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107867686 | GATGATAGAAAAGGA[C/T]AGATTTGAATTATAT | 11043 |
rs150559268 | snp | A/G | 0.0399626 | 0.135589 | intron-variant | MID2 | GRCh38.p7 | X:107883075 | ATGAAGCTGGAAACC[A/G]TCATTCTCAGCAAGC | 11043 |
rs150570766 | snp | A/G | 0.00339864 | 0.0410825 | synonymous-codon, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107926098 | TTATTTTTCAGGCCA[A/G]CCCTTTAAATTGGAT | 11043 |
rs150699274 | snp | C/G/T | | | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107916703 | CTATATTAAATAGCT[C/G/T]CTCCTTATTGAACAT | 11043 |
rs150700426 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | MID2 | GRCh38.p7 | X:107832547 | AATAGCCCGTGAGAT[A/G]GGCAGGGCAGGTATT | 11043 |
rs150716868 | snp | C/T | 0.000410964 | 0.0143287 | synonymous-codon, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107926152 | GAAGATCTCCAATGA[C/T]GGATTGCAGATGGAG | 11043 |
rs150718851 | snp | C/G | 0.0525796 | 0.153379 | intron-variant | MID2 | GRCh38.p7 | X:107887385 | TATTGAGATAATCAT[C/G]TGGTTTTTGTCTTTG | 11043 |
rs150859176 | snp | G/T | 0.00738971 | 0.0603345 | intron-variant | MID2 | GRCh38.p7 | X:107869485 | ATAATTTTGTATAGT[G/T]ACAAAATATACTCAG | 11043 |
rs151014962 | snp | C/T | 0.0105399 | 0.0718252 | intron-variant | MID2 | GRCh38.p7 | X:107876142 | CAGTTAACAGGTGCA[C/T]CTCAGGAATCCTGGG | 11043 |
rs151034854 | snp | C/G | 0.00158814 | 0.0281345 | intron-variant | MID2 | GRCh38.p7 | X:107851443 | TCCTGAAACACATTT[C/G]TTTCAATTATCCTCA | 11043 |
rs151065224 | snp | C/G/T | 0.000189982 | 0.00974449 | missense | MID2 | GRCh38.p7 | X:107841164 | TGTGACCGTTGCCTG[C/G/T]GGGCCACGCACCCCA | 11043 |
rs151103676 | snp | A/G | 0.0409784 | 0.137149 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107901423 | TGGAAGCCAGATCTG[A/G]AGAGAAGGTGATAAG | 11043 |
rs151156360 | snp | A/G | 0.00896606 | 0.0663524 | intron-variant | MID2 | GRCh38.p7 | X:107866817 | AAGGCTAACATCATT[A/G]CCATCATTAACATCT | 11043 |
rs151224413 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107921744 | TTACAGCCCTTACTT[A/G]TGTTGGTGTTCAAAT | 11043 |
rs151227115 | snp | G/T | 0.0256233 | 0.11025 | intron-variant | MID2 | GRCh38.p7 | X:107835201 | ATGTTGAAGTATGTA[G/T]CAGAACTTCATTCCT | 11043 |
rs151244156 | snp | C/T | 0.0214859 | 0.101397 | intron-variant | MID2 | GRCh38.p7 | X:107891121 | CGCTGCACCCACTGT[C/T]CTGCACCCTCTTTCT | 11043 |
rs180671837 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107850036 | TGAGAAAGTTGCACT[A/G]ACCGGGCTTGAACAT | 11043 |
rs180677775 | snp | C/T | | | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107901845 | ACTTTCCAAGTAAAA[C/T]GACAATCTCGGGCAA | 11043 |
rs180684401 | snp | A/G | 0.00844089 | 0.0644143 | intron-variant | MID2 | GRCh38.p7 | X:107860565 | TTGTTTGTCACTCAC[A/G]ATACAATAACAAACT | 11043 |
rs180691544 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | MID2 | GRCh38.p7 | X:107883044 | GTATGAGTTCCTGTC[A/G]TTTGCAGGGACATGG | 11043 |
rs180698921 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | MID2 | GRCh38.p7 | X:107829677 | CTCCTGCTTGTTCCA[C/T]GCCAAACTCCATACT | 11043 |
rs180715008 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | MID2 | GRCh38.p7 | X:107872801 | TGGGCCAAAGAAGTT[A/G]TATGTTTAATCAAAT | 11043 |
rs180719220 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107914701 | TTTAGAAGATCTTGC[A/G]CAGGACTAAAACATG | 11043 |
rs180725442 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | MID2 | GRCh38.p7 | X:107893557 | CTTTTAAAAAGGAAC[A/G]ATTAAGTAGATATAT | 11043 |
rs180819589 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107837861 | GCTTAACATAGTACT[C/G]AGAATACAGGAGATG | 11043 |
rs180933308 | snp | A/G | | | intron-variant | MID2 | GRCh38.p7 | X:107833251 | CATCTTAAAGAGATC[A/G]TCTGGTGATTCTAGT | 11043 |
rs180942568 | snp | A/C | 0.0147244 | 0.0845304 | intron-variant | MID2 | GRCh38.p7 | X:107867493 | AAAGTTTATACTGCC[A/C]CTCTGCTGGGTTAAG | 11043 |
rs180954108 | snp | A/T | 0.294351 | 0.246034 | intron-variant | MID2 | GRCh38.p7 | X:107845523 | CACACACACACACAC[A/T]CACTCTCTCTCTCTC | 11043 |
rs180955014 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107879155 | AGAGTGTTACAATCA[A/G]TGCTCTTTCAGCTTT | 11043 |
rs180956107 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107919368 | AATGAGGGAGTCAAG[A/G]TTGCAGCTTGAGCCT | 11043 |
rs180993872 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB, utr-variant-5-prime | MID2 | GRCh38.p7 | X:107824238 | CTAATTTTATTTTTT[A/G]TAGAGACACGTTCTA | 11043 |
rs180998206 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107897703 | TGTGTATGTGTGTGC[A/G]TGTGAGAGAGTGTGA | 11043 |
rs181105219 | snp | A/T | 0.000529661 | 0.016265 | utr-variant-3-prime, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107928015 | TACTTGAGGATGGCC[A/T]TCTGAATTGTTAAAA | 11043 |
rs181304981 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | MID2 | GRCh38.p7 | X:107856102 | CTTCGACTTCTTTCT[A/G]GGTATCACAGGTCAT | 11043 |
rs181319269 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107898149 | CTTGCTCTCAACTAA[A/G]ATGTCAATTAACAAT | 11043 |
rs181331802 | snp | G/T | 0.00158814 | 0.0281345 | intron-variant | MID2 | GRCh38.p7 | X:107880112 | CTCTCAGAATTTGGG[G/T]ACTAGGGTTTTTCTT | 11043 |
rs181352368 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107920024 | CTTCTATTTCTTCCT[C/T]TAGTTATTGATAGAA | 11043 |
rs181420437 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | MID2 | GRCh38.p7 | X:107865901 | GTTTTGCACTGGCAT[A/G]GAATGGCAGGTTTAC | 11043 |
rs181432456 | snp | C/T | | | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107907197 | AAGAGGTTGGTACTA[C/T]TGCATCACAAATGTA | 11043 |
rs181437869 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | MID2 | GRCh38.p7 | X:107866317 | TATCACAGATGAATA[C/T]GCAAATTGCATATTG | 11043 |
rs181448334 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107844448 | CTCTCACTTTTCACT[C/T]ACTAGTCCCAATATA | 11043 |
rs181478058 | snp | G/T | 0.00475684 | 0.0485365 | intron-variant | MID2 | GRCh38.p7 | X:107889801 | GTCTCATATTTTTTG[G/T]AGGCTTCGTTCATTT | 11043 |
rs181507296 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107844056 | TATTTTTACTTTTTG[A/G]TTCTGGAACTTCACT | 11043 |
rs181528585 | snp | A/G | 0.0220041 | 0.102557 | intron-variant | MID2 | GRCh38.p7 | X:107889481 | TGTAGAGTTTCTGCC[A/G]AGAGATCCGCTGTTA | 11043 |
rs181588142 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB, utr-variant-5-prime | MID2 | GRCh38.p7 | X:107823911 | CCCTTGTGTATATAT[A/G]CCATATTTTCTTTAT | 11043 |
rs181625469 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107829011 | CAGCTTCCTTAGTAG[C/T]TGGGACTATAGGCAC | 11043 |
rs181629049 | snp | G/T | 0.00791544 | 0.0624105 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107908287 | ATATTTTTATGCCAC[G/T]TCCTTCCTCTCTATT | 11043 |
rs181642455 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | MID2 | GRCh38.p7 | X:107871345 | TTGCAGGAGGGGGAG[C/T]GCAGGTGAGCAGGTG | 11043 |
rs181658654 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | MID2 | GRCh38.p7 | X:107848771 | TGTTGTTGAGAGGCC[A/G]TATGTAATTGATACA | 11043 |
rs181772254 | snp | A/G | | | intron-variant | MID2 | GRCh38.p7 | X:107839403 | TTTTTTGGCAGTCTC[A/G]CTCTGTCACCCAGGC | 11043 |
rs181799114 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | MID2 | GRCh38.p7 | X:107883346 | CCCAGAACTTAAAGT[A/G]TAATTTAAAAAAATG | 11043 |
rs181842437 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107909113 | TATTTTTGTATTCCT[A/G]TAAATATTCTTAAAC | 11043 |
rs182024718 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107871954 | GTGTTCTCACTTTGG[A/G]ACACGGTTCCAGGCT | 11043 |
rs182056391 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107893138 | TCTGTCTATAATCTT[C/T]CATGTTCTTACGGCT | 11043 |
rs182062610 | snp | C/G | 0 | 0 | intron-variant | MID2 | GRCh38.p7 | X:107861516 | TCCCAGCTACTCAAG[C/G]GGCTGAGGCAGGAGA | 11043 |
rs182063042 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107914240 | GCCTGGCACATTAGT[C/T]GTGCTTAATAAGTAT | 11043 |
rs182073660 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107860975 | ACCACTCCATTACGC[A/G]TTGTTTTGCAAGACC | 11043 |
rs182117017 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | MID2 | GRCh38.p7 | X:107862723 | GTCACATGCTTTCAT[C/T]TCTAGTAATTTTAAA | 11043 |
rs182119172 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107831552 | AGCCCTTTGTTCAGT[A/G]TTGCTAGGATCCATG | 11043 |
rs182122872 | snp | A/G | 0.0440191 | 0.141675 | intron-variant | MID2 | GRCh38.p7 | X:107885402 | TTGCGATAGTTTGCT[A/G]AGAATGATGGTTTCC | 11043 |
rs182132222 | snp | A/C/T | 4.87315e-05 | 0.00493597 | missense, synonymous-codon | MID2 | GRCh38.p7 | X:107841359 | CATCAGGTCGCATCC[A/C/T]TGAATGATCGATTTG | 11043 |
rs182136911 | snp | G/T | 0.000302656 | 0.0122978 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107903948 | GTAATACTCTGAAAT[G/T]TCTTGGCAGGTGAAT | 11043 |
rs182151272 | snp | A/T | 0.00211696 | 0.0324653 | utr-variant-3-prime, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107929841 | AAAGACACCCCAAGC[A/T]TCCCCCTCTCTCAGC | 11043 |
rs182254893 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107829238 | GTGGATTGACTGGGT[A/G]TAAGCAGGAATCTTA | 11043 |
rs182324186 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107902931 | AATGGAACTGAACCT[C/T]GCCCGCCCACCCAGC | 11043 |
rs182368646 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107834496 | TAACTCTGTATAGAT[G/T]AGTGATTCACAAACT | 11043 |
rs182433834 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant, nc-transcript-variant | MID2, LOC101928335 | GRCh38.p7 | X:107895787 | GAAAGAACACTGGAT[A/G]GGACTCAGAAGATCT | 11043 |
rs182441041 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107853112 | GCCCATGATTAATCT[A/G]GAGTGAAATGATACT | 11043 |
rs182445338 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | MID2 | GRCh38.p7 | X:107893659 | TGACTTATTAATAGT[A/G]ATATGCTCACTGGGA | 11043 |
rs182456377 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107873840 | GATGGTATTTAATGG[A/G]ACTCCCATTACCTGT | 11043 |
rs182546036 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107849410 | GAGGTGGTGTCTTGA[C/T]GTACGCCTAGTTTTC | 11043 |
rs182554633 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107884555 | CTGGCTTACAATCCA[C/G]ACTTTTTCCCACTCT | 11043 |
rs182659744 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107875805 | GCTAAGAGAAGAGAA[A/G]GGGCCCGGATTGGAG | 11043 |
rs182694549 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107916597 | ATGAGGGATGCAACC[A/G]GCCTGTTAAAAATGC | 11043 |
rs182694840 | snp | A/C | 0.00528398 | 0.051128 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107900187 | ATGTGACTGTCCAAA[A/C]AACATTCCCACCCTA | 11043 |
rs182697775 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107924044 | AAGAGTGATGATTCC[A/G]TGACTCTGTATAGTA | 11043 |
rs182740540 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107898812 | GAGATCTATTTGGGC[A/T]GAAGATTTCAGAGAA | 11043 |
rs182749309 | snp | A/C | 0.0204488 | 0.0990265 | intron-variant | MID2 | GRCh38.p7 | X:107826953 | CCTTTTCTGCCAGGG[A/C]GCGATCCTCGAGTCT | 11043 |
rs182759319 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107922034 | ATATGCACACATATA[A/T]AATAACACATGCATA | 11043 |
rs182765561 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | MID2 | GRCh38.p7 | X:107869882 | GGCACTTATATCTCC[C/T]TTACCAATATTTATA | 11043 |
rs182773133 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | MID2 | GRCh38.p7 | X:107890887 | GTGCTAGCAATTAGC[A/G]AGGCTCTGTGGGATT | 11043 |
rs182827914 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | MID2 | GRCh38.p7 | X:107859222 | AAAATAAATTAATTT[A/T]AAAAACACTGCTATG | 11043 |
rs182838382 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107881827 | TTAAGTATAGAACAA[A/G]CATTAGATGAATGAT | 11043 |
rs182842926 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | MID2 | GRCh38.p7 | X:107836075 | ACTTCATCCTCTTGC[A/C]TGTGGATATCCAGTT | 11043 |
rs182905785 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107841701 | TATATCTTTGCTATG[A/G]TCTTTCCACCTCTTC | 11043 |
rs182922606 | snp | A/G | 0.00896606 | 0.0663524 | utr-variant-3-prime, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107931625 | ATTAAATAAATATAT[A/G]TGTATTCATGAATTC | 11043 |
rs182923045 | snp | A/G | 0.0440191 | 0.141675 | intron-variant | MID2 | GRCh38.p7 | X:107885969 | CTTTTTGATGGGGTT[A/G]TTTGTTTTTTTCTTG | 11043 |
rs182952565 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | MID2 | GRCh38.p7 | X:107830412 | CATTTCCATTTAGCA[C/T]TAAGTTTTTGTCCTC | 11043 |
rs182958894 | snp | C/T | | | intron-variant | MID2 | GRCh38.p7 | X:107850694 | GGCAAACTAACCATT[C/T]GCCATAATTTTGTGA | 11043 |
rs183172710 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107868662 | GGAAGTAAAATCATT[C/T]ACTACGATTTTACTA | 11043 |
rs183177942 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB, utr-variant-5-prime | MID2 | GRCh38.p7 | X:107825021 | CCATTTTCTCATTTC[C/T]TTCCCCTTCTTCTCC | 11043 |
rs183179584 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107863381 | TCATGTCTTCATAGC[C/T]GAAACAGTTCACATA | 11043 |
rs183202959 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107911878 | GATTGGAGGGGCAGC[A/G]GTGTGGAAGGTATAA | 11043 |
rs183224249 | snp | A/C | 0.00896606 | 0.0663524 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107910168 | ATTCCCTCCTCATAC[A/C]AGCCTCTAGTAACCA | 11043 |
rs183225627 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107904816 | ATGGTTTTAGGCTTG[C/T]TGGCTTGCTCGTCAG | 11043 |
rs183244095 | snp | A/T | | | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107915971 | TTGCAACCTATTTTG[A/T]TGTATATTGATGTAC | 11043 |
rs183258496 | snp | A/G | 0.00949095 | 0.0682305 | intron-variant | MID2 | GRCh38.p7 | X:107857593 | GCCAACTTCCTCTTA[A/G]TAATAACAACGGTGA | 11043 |
rs183423992 | snp | A/G | 0.0157677 | 0.0873799 | intron-variant | MID2 | GRCh38.p7 | X:107846381 | TAAGGTCTGGTGGTA[A/G]TGGTGGTGAACATGT | 11043 |
rs183440062 | snp | C/G | 0.00158814 | 0.0281345 | intron-variant, nc-transcript-variant | MID2, LOC101928335 | GRCh38.p7 | X:107895053 | TGCTAAAATAATACA[C/G]AGAGTTCCCACATAC | 11043 |
rs183459887 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | MID2 | GRCh38.p7 | X:107890440 | GAACAGTGGATATTG[A/G]TGAACAGCAGATGTT | 11043 |
rs183472144 | snp | C/G | 0.00158814 | 0.0281345 | intron-variant | MID2 | GRCh38.p7 | X:107833722 | AAGGCTAGATTTGGA[C/G]GACAATGCTGAAATC | 11043 |
rs183488772 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107880588 | AAAAAACCTGAAAAG[A/G]TATCTCAAAAGGCCA | 11043 |
rs183518970 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107889359 | CATCTGTAAAGGCTT[C/T]TATTTCTCCTTCACT | 11043 |
rs183527018 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107906164 | TTGCAGATCCTTAGA[A/G]GCCCATCCATAGACC | 11043 |
rs183528551 | snp | A/G | 0.00633741 | 0.0559334 | intron-variant | MID2 | GRCh38.p7 | X:107865763 | AGGCACAAAACAATC[A/G]CTGGCTTTGGAATAA | 11043 |
rs183543869 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | MID2 | GRCh38.p7 | X:107840199 | TTTCAGGAAGTAGAG[A/G]GTTACTTTAAAATAT | 11043 |
rs183778498 | snp | A/G | 0.0121112 | 0.0768695 | intron-variant | MID2 | GRCh38.p7 | X:107881480 | CTCTTTGTTCTGCCC[A/G]GTGATGACCTTTTCT | 11043 |
rs183799064 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107922803 | ATCAGTTCATAGTGA[C/T]CTTTTCCTCATTTTT | 11043 |
rs183976635 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107858413 | ATAGCCAAGGGAAAA[G/T]GTATACCAACAGATG | 11043 |
rs183997740 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107899708 | ACAAGTAGGTTGCCA[A/G]GATTGACCTAATGGT | 11043 |
rs184019386 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107901930 | GTGACTAATGAGAAA[C/T]GGATGACAGAATAAA | 11043 |
rs184031008 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107883197 | TACACACTGGGGCCT[A/G]TCGGGGAGTGGGGGG | 11043 |
rs184039524 | snp | A/G | 0.000529661 | 0.016265 | utr-variant-3-prime, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107927285 | ATCTGAGTAGTCTGC[A/G]TTCAAGCCATTGGAG | 11043 |
rs184049011 | snp | G/T | 0.00949095 | 0.0682305 | intron-variant | MID2 | GRCh38.p7 | X:107830801 | ATCTTCTTGTACAGA[G/T]AGCTAATCTACTTTT | 11043 |
rs184098439 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107875197 | GTAATGGTATGCAGA[A/G]GAAGGCATCCTTTAG | 11043 |
rs184102374 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107875874 | GTCCACTTTCCTCCC[G/T]TTGATTTTCAGAACT | 11043 |
rs184108871 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107832104 | TAATTATTGAAAAGA[A/G]CATACATTAATTCCA | 11043 |
rs184111850 | snp | A/G | 0.00791544 | 0.0624105 | intron-variant | MID2 | GRCh38.p7 | X:107853538 | CTCCTGGGCTCAAGC[A/G]ATCTGCCCACCTCAG | 11043 |
rs184115237 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107917429 | GAGATGTTGGGTTAC[A/G]CAGGAAGAGTAACAA | 11043 |
rs184141966 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, nc-transcript-variant | MID2, LOC101928335 | GRCh38.p7 | X:107896001 | AAATTTTATAGCTAT[A/G]TACATAAAATACCAG | 11043 |
rs184241054 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | MID2 | GRCh38.p7 | X:107852702 | CCAGCCTGCAAACAC[A/G]TGTATCTATGTGAAT | 11043 |
rs184306311 | snp | A/G | 0.017851 | 0.0927731 | intron-variant | MID2 | GRCh38.p7 | X:107843474 | TTTTGGAGAAAGAAA[A/G]CCAGATTTTGAATAG | 11043 |
rs184432578 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107829116 | ACTCCTGAGCTTAAG[A/G]GATCCACCTGCCAAG | 11043 |
rs184432772 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107924827 | TCTTACTACAGAGAA[A/G]CCATATCTGTTAGGA | 11043 |
rs184638563 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | MID2 | GRCh38.p7 | X:107891311 | TTTGAGAAAGAGTCT[C/T]ACCTTGTCACCCAGG | 11043 |
rs184640136 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | MID2 | GRCh38.p7 | X:107837645 | AGATAAACCTCAGTG[A/C]AGGAGGTGAGATGAT | 11043 |
rs184643756 | snp | A/G | 0.0214859 | 0.101397 | intron-variant | MID2 | GRCh38.p7 | X:107892349 | TCACCCACTAGTCAC[A/G]TGAACTTGGGTGGAA | 11043 |
rs184645111 | snp | G/T | 0.00158814 | 0.0281345 | intron-variant | MID2 | GRCh38.p7 | X:107860144 | AGAGATGAAGGCCCA[G/T]CTTGAGACAGTGGCA | 11043 |
rs184653231 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107870401 | GTTGTGTGAGAATGA[C/T]TTGTTCTTTCAAAGT | 11043 |
rs184705068 | snp | C/T | 0.104598 | 0.203367 | intron-variant | MID2 | GRCh38.p7 | X:107889489 | TTCTGCCGAGAGATC[C/T]GCTGTTAGTCTGATG | 11043 |
rs184713448 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107844204 | AATAACCAGAAACTA[A/G]CCTGTCTTTTTAACA | 11043 |
rs184724956 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | MID2 | GRCh38.p7 | X:107865559 | ACCTGTTTCCCTCCC[C/T]GCCCACCCCAAAGGG | 11043 |
rs184728276 | snp | A/T | 0.00528398 | 0.051128 | intron-variant | MID2 | GRCh38.p7 | X:107886790 | TGTTTGTATCCTCTT[A/T]TATTTCATTGAGCAG | 11043 |
rs184773460 | snp | A/G | | | intron-variant | MID2 | GRCh38.p7 | X:107871122 | ATTTTGGTATTTAGT[A/G]TGTGCTCTTTCATTA | 11043 |
rs184801436 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107912541 | GAACACTCCTGGTTT[C/T]CTTCCTACTTTGTTG | 11043 |
rs184855419 | snp | A/G | 0.022522 | 0.1037 | intron-variant | MID2 | GRCh38.p7 | X:107842630 | GTTGCAAATAATATT[A/G]AGAGTAGTCACAATG | 11043 |
rs184858361 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | MID2 | GRCh38.p7 | X:107866028 | GAAGGATAACAATGC[C/T]ATGTGAAAAGGAAGG | 11043 |
rs184869720 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107907827 | TACTATAAGTCATAT[G/T]GCAAGAAATAGCAAT | 11043 |
rs184891922 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107891858 | GGCTCTTCTTCAGCT[A/G]TTTTCACTCTTCTAC | 11043 |
rs184897924 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107848746 | AGTTTGTGAACCAGA[C/T]GGCATGTTCTGTTGT | 11043 |
rs184957590 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107918642 | TGGGGATCAAACTCT[A/G]AAAAACATTTGCTTC | 11043 |
rs184962036 | snp | A/T | 0.00949095 | 0.0682305 | intron-variant | MID2 | GRCh38.p7 | X:107828480 | CCACACCCAGCTAAT[A/T]TTTGTATTTTTTGTA | 11043 |
rs184977536 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | MID2 | GRCh38.p7 | X:107833339 | CCTTACCCCAAGGCA[G/T]GGAGACAGTTTCTAA | 11043 |
rs185027661 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107859640 | AATGAATGTAAATGC[A/G]TGATGACAAGTTAGC | 11043 |
rs185070346 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107900760 | CATGCATCTTTCCTT[C/T]ACTTACCCACCAAAA | 11043 |
rs185152752 | snp | A/T | 0.00791544 | 0.0624105 | intron-variant | MID2 | GRCh38.p7 | X:107836567 | ACTTTTTTTTTTTTT[A/T]AAATAATGATAATAC | 11043 |
rs185171489 | snp | A/G | 0.00738971 | 0.0603345 | intron-variant | MID2 | GRCh38.p7 | X:107882372 | GATCTAATTAAACTA[A/G]AGAGCTTCTGCACAG | 11043 |
rs185278487 | snp | C/T | 0.00896606 | 0.0663524 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107921624 | ATTTTCAAGTTGGCA[C/T]TTGGCATTCTACTAT | 11043 |
rs185436110 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107909117 | TTTGTATTCCTATAA[A/T]TATTCTTAAACTTTG | 11043 |
rs185451419 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107898318 | GGCTGATCTGCTTTA[A/C]CCAAGCACGTTTTCT | 11043 |
rs185452474 | snp | A/G | 0.00475684 | 0.0485365 | intron-variant | MID2 | GRCh38.p7 | X:107889947 | CATCACATAGTTCTC[A/G]TGCCATGGTTTTCAG | 11043 |
rs185461689 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107857189 | TTCTGTCTTTGATGA[C/T]AGGGACCCTACAGGA | 11043 |
rs185464994 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107848060 | GGTTAAAATTTAGGC[G/T]TTACCAGTGGCTGAA | 11043 |
rs185469167 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | MID2 | GRCh38.p7 | X:107880507 | CTTGCATGCTGAGTC[A/G]CTTCTGGGTCGGAGC | 11043 |
rs185510497 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107860727 | TTATCTTAAAGACTA[C/T]AATAATAAGTAACAC | 11043 |
rs185517028 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107830069 | CCTCCCATAAAATCT[A/G]CTGACACCACAATAA | 11043 |
rs185520085 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107925315 | AGAGAGAAAAAGTTG[C/G]GAAAGGGTAATGTGT | 11043 |
rs185526209 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107882767 | GTGGGACTGTAAACT[A/C]GTTCAACCATTGTGG | 11043 |
rs185566045 | snp | C/T | | | intron-variant | MID2 | GRCh38.p7 | X:107878348 | AGAGGAAACTCACTG[C/T]GTGCCATGCATGTCT | 11043 |
rs185574339 | snp | C/T | 0.000182692 | 0.00955577 | missense, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107905535 | CGCCAGTGTCTTGAA[C/T]GGTCAACAGTCCTCA | 11043 |
rs185579133 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | MID2 | GRCh38.p7 | X:107832936 | ACAGCCCCCAAATAT[A/G]TTCTCATTAGTTTAT | 11043 |
rs185591375 | snp | A/G | 0.00633741 | 0.0559334 | intron-variant | MID2 | GRCh38.p7 | X:107827917 | TTATGTGTTTGTTAT[A/G]GTTTGGATATTTATC | 11043 |
rs185640820 | snp | A/T | 0.00158814 | 0.0281345 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107901614 | CATAAGACACAATTC[A/T]TGCCCTCCAGAACTC | 11043 |
rs185687682 | snp | A/T | | | intron-variant | MID2 | GRCh38.p7 | X:107854385 | CAATAAATTCCTACA[A/T]CCACAAAGTCATGAA | 11043 |
rs185731529 | snp | A/T | 0.0068637 | 0.0581785 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107896814 | GCCTCTCTCTCTCTC[A/T]CACACACACACACAC | 11043 |
rs185971285 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | MID2 | GRCh38.p7 | X:107850965 | TGTTTGAATGGAAAT[A/G]CATTACAGTTGGAAA | 11043 |
rs185991912 | snp | C/T | 0.0068637 | 0.0581785 | intron-variant, downstream-variant-500B | MID2, LOC101928335 | GRCh38.p7 | X:107894232 | ACATGGCTTGGTACA[C/T]GAATAGGTACCGAGA | 11043 |
rs186007782 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | MID2 | GRCh38.p7 | X:107874385 | GTTAAGTTATTCCCC[A/G]TGGTTAACTTAGTAG | 11043 |
rs186056125 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107897821 | TGTTCATAAACATTG[C/T]GTTTTCTTAAATGCA | 11043 |
rs186062474 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107867549 | GAGACAGAGGGGCCA[A/G]TTAGGAGACTGTAGT | 11043 |
rs186070262 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB, utr-variant-5-prime | MID2 | GRCh38.p7 | X:107824321 | CTCAGCATCCCCTCC[C/T]GAGTAGCTGGGATTA | 11043 |
rs186203367 | snp | A/T | 0.00949095 | 0.0682305 | intron-variant | MID2 | GRCh38.p7 | X:107879187 | CCATCCACATATGGC[A/T]TAAGTGTTAACAGCT | 11043 |
rs186405344 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107872993 | CTGAGGTGCATTTTG[A/G]TAATATTCATCTTTT | 11043 |
rs186408491 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107914900 | TTACTGGTTGTGTGA[A/T]CTTGGACAAGTTACT | 11043 |
rs186422985 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | MID2 | GRCh38.p7 | X:107861569 | AGGTTGCAGTGAGCC[A/G]AGATCGTGCCATTGC | 11043 |
rs186426345 | snp | C/T | 0.0440191 | 0.141675 | intron-variant | MID2 | GRCh38.p7 | X:107885386 | GTTTGGTTTTTTGTC[C/T]TTGCGATAGTTTGCT | 11043 |
rs186429520 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107840428 | GTTAATCAGTCTATC[A/G]GGATTCAGAGGTGGC | 11043 |
rs186433878 | snp | A/G | 0.00791544 | 0.0624105 | intron-variant | MID2 | GRCh38.p7 | X:107893275 | CACTTCGGGTAAAAA[A/G]CACAGTCTTTGTCAG | 11043 |
rs186437697 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107914286 | AGGAAATAAAGAAGA[C/T]TGGAGAGGCCAGAAA | 11043 |
rs186456104 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | MID2 | GRCh38.p7 | X:107866391 | ACTCCATTTCTGTCA[A/G]AAACAGGATATCAGC | 11043 |
rs186465752 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107889809 | TTTTTTGGAGGCTTC[A/G]TTCATTTCTTTTTTT | 11043 |
rs186473987 | snp | A/G | | | intron-variant | MID2 | GRCh38.p7 | X:107844487 | TTCATGATATATGGG[A/G]CATTTCTATAAAACG | 11043 |
rs186479744 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107908330 | TACATGTATATTTGG[C/T]TGTCTGAAATTGTCC | 11043 |
rs186583025 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107850061 | GAACATAAGGAACCT[G/T]GCCCAGTCATTAACT | 11043 |
rs186627936 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107893568 | GAACGATTAAGTAGA[C/T]ATATTTTATCTTGTT | 11043 |
rs186817148 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107912379 | TCCCACTACCACACC[A/G]TTGAAAGTATTCTTT | 11043 |
rs186853917 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | MID2 | GRCh38.p7 | X:107839967 | TTGATGAACTGAAGG[G/T]GTTTCTGAAGGTGAG | 11043 |
rs186896352 | snp | C/T | | | intron-variant | MID2 | GRCh38.p7 | X:107861217 | GATTTGATGAGTCAA[C/T]TGGAGCAGAAGCATA | 11043 |
rs186917575 | snp | C/G | 0.00475684 | 0.0485365 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107902482 | TTAGGGAAAGGGTGA[C/G]GTGTCTGAGAAAAAA | 11043 |
rs186921660 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107881592 | CAGGGATCTGCCTTT[G/T]CATAAAGGACATACG | 11043 |
rs186931925 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107834959 | AGTTGTGCAATCATC[A/G]TCACTATCTAATTTT | 11043 |
rs186936376 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | MID2 | GRCh38.p7 | X:107858553 | CATTTATTGAGCATA[C/T]GCTGTGTACTCTGTG | 11043 |
rs186981777 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107859426 | GTTGAAGGAGAAAAA[A/C]AATTACTCCCTCTGG | 11043 |
rs186991228 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | MID2 | GRCh38.p7 | X:107882153 | AACTGGCTAGCCATA[G/T]GTAGAAAGCTGAAAC | 11043 |
rs187002903 | snp | C/T | | | utr-variant-3-prime, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107929008 | TGTACCATTTATTAG[C/T]GTTGTGACCTAGGAC | 11043 |
rs187016606 | snp | C/G | 0.0173306 | 0.0914601 | upstream-variant-2KB, utr-variant-5-prime | MID2 | GRCh38.p7 | X:107825597 | GGGGTTGGGGGACAG[C/G]GGGATTGGGGAGTGG | 11043 |
rs187024460 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107900197 | CCAAAAAACATTCCC[A/C]CCCTAGCTCCCTCAT | 11043 |
rs187024671 | snp | G/T | | | missense, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107924469 | TAAACCAAGCCGGCA[G/T]CCGGAACAGTGAACC | 11043 |
rs187074650 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107883798 | ATTATTGTTTGAACA[C/T]AGTCTATGGGAAAGT | 11043 |
rs187102939 | snp | C/T | 0.000529661 | 0.016265 | utr-variant-3-prime, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107928114 | TTTTAAAAAGTTGCA[C/T]AGTGAAGGCTCTTTA | 11043 |
rs187196855 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107903042 | CACTAAAATTCTCTA[C/T]GCCTCAGTTTCCCCG | 11043 |
rs187214500 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | MID2 | GRCh38.p7 | X:107833872 | AATTACGGCTTACTG[C/T]AGCTTCGACCTGCTG | 11043 |
rs187226550 | snp | A/G | 0.00475684 | 0.0485365 | intron-variant | MID2 | GRCh38.p7 | X:107863082 | AAACCTAAGTTAACT[A/G]TGCAATCCAGTGTGT | 11043 |
rs187228108 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | MID2 | GRCh38.p7 | X:107831860 | CATTTGTTCCTCAAC[C/T]CTGCAACTGCCAGTG | 11043 |
rs187231234 | snp | A/C/G | 0.00211696 | 0.0324653 | intron-variant | MID2 | GRCh38.p7 | X:107880938 | AAGTTTTGCAAAGGC[A/C/G]ATTTCAAAATTGTAT | 11043 |
rs187252547 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | MID2 | GRCh38.p7 | X:107885635 | CCTTTGGGTATATAC[C/T]CAGTAATGGGATGGC | 11043 |
rs187254720 | snp | A/T | 0.000529661 | 0.016265 | utr-variant-3-prime, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107930335 | CTACATAATAAATGA[A/T]CATTGTCCTCCTCAA | 11043 |
rs187259382 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107853187 | AACATGCTAGAATTC[C/T]GGCTACTGTTGTAAC | 11043 |
rs187297845 | snp | A/G | 0.00475684 | 0.0485365 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107922074 | TATATGTGCATATTT[A/G]TGTGCACATACACAA | 11043 |
rs187346277 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | MID2 | GRCh38.p7 | X:107872336 | TCTAATGCTGAAGAT[C/T]ACAGAAATAAGAAGT | 11043 |
rs187347708 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107829365 | AATGAAAACATACAT[A/G]CAACTAGGCATACAG | 11043 |
rs187462719 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107898902 | GGAATTCCTTGCCAT[A/G]TAATTATTATTATTA | 11043 |
rs187468055 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107830601 | ATTTTGATAAATGAA[A/G]TTTTGGTACCAAGAT | 11043 |
rs187468989 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107857753 | GAAAATGAAATGTAT[A/G]GTAGAATACTGTCAG | 11043 |
rs187541063 | snp | A/T | | | intron-variant | MID2 | GRCh38.p7 | X:107842648 | AGTAGTCACAATGAC[A/T]ATGGTTTGTGCCTCT | 11043 |
rs187564232 | snp | A/G | 0.0019273 | 0.0309828 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107916145 | GTGTGAAAATACTGT[A/G]CTTTCCTTTCCATTT | 11043 |
rs187567498 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107865566 | TCCCTCCCCGCCCAC[A/C]CCAAAGGGTTCTTTT | 11043 |
rs187570559 | snp | C/T | 0.00182567 | 0.0301579 | synonymous-codon, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107905555 | AACAGTCCTCATCAA[C/T]CAAGCTGAGCATATC | 11043 |
rs187584466 | snp | A/T | 0.00791544 | 0.0624105 | intron-variant | MID2 | GRCh38.p7 | X:107886955 | ATAAGAATGCTTGTG[A/T]TTTTTGCACATTGAT | 11043 |
rs187704693 | snp | A/G | | | intron-variant | MID2 | GRCh38.p7 | X:107828331 | TTTTTTTTTTTTTTG[A/G]GACAGGGTCTTGCTT | 11043 |
rs187743732 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107899937 | TGTCTTCAAACAAAG[A/G]AAATACCAGGGGCTT | 11043 |
rs187756087 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107870720 | AGTGTAAGTTTTCAC[A/G]CCATGGAAATCAGCA | 11043 |
rs187780069 | snp | A/G | | | intron-variant, nc-transcript-variant | MID2, LOC101928335 | GRCh38.p7 | X:107895900 | TTAAGTGATGGAGTA[A/G]GAATCGATTATTTCT | 11043 |
rs187803624 | snp | A/G/T | 0.00105904 | 0.0229869 | intron-variant | MID2 | GRCh38.p7 | X:107890444 | AGTGGATATTGGTGA[A/G/T]CAGCAGATGTTGCTG | 11043 |
rs187816681 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | MID2 | GRCh38.p7 | X:107847147 | GCATCAGGGATTTAG[A/G]CTAGGGATTCATTCA | 11043 |
rs187824377 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107827121 | ATTAAGTAAATAACG[C/G]CGGAGTAGATTTACA | 11043 |
rs187830345 | snp | C/T | 0.00949095 | 0.0682305 | intron-variant | MID2 | GRCh38.p7 | X:107891072 | GCTTCCTGGGTGAGG[C/T]GATGCCTCACCCTGC | 11043 |
rs187844701 | snp | A/G | | | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107911074 | GGCCAGGGTGGTCTC[A/G]AACTCCTGATCTCCA | 11043 |
rs187846964 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | MID2 | GRCh38.p7 | X:107869955 | CATTTAAAACACTAT[A/G]GTGATATCAGACATC | 11043 |
rs187956478 | snp | C/T | 0.00475684 | 0.0485365 | intron-variant | MID2 | GRCh38.p7 | X:107846839 | TCTCTTCACCAATAT[C/T]TGAAAGGAGCTAACA | 11043 |
rs188015988 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107922821 | TTTCCTCATTTTTTT[C/T]ACAGCTGCATAGTAC | 11043 |
rs188020221 | snp | C/T | 0.00528398 | 0.051128 | intron-variant | MID2 | GRCh38.p7 | X:107891341 | GCTGGAATGCAGTGG[C/T]GCAATCTCAGCTCAT | 11043 |
rs188032158 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | MID2 | GRCh38.p7 | X:107848114 | TTGGGAGTCCTCAGC[A/G]TGGTGGTAGAGCCAT | 11043 |
rs188053779 | snp | C/T | 0.000799051 | 0.0199722 | intron-variant | MID2 | GRCh38.p7 | X:107841403 | AAGGGATCTGGGGAG[C/T]ATCCCCTATACAACT | 11043 |
rs188057415 | snp | A/T | 0.163039 | 0.234388 | intron-variant | MID2 | GRCh38.p7 | X:107833427 | TATATATATATATAT[A/T]TATTTTTTTTAAAAA | 11043 |
rs188059161 | snp | A/G | 0.00581083 | 0.0535878 | intron-variant | MID2 | GRCh38.p7 | X:107889409 | GGATATGAAATTCTG[A/G]GTTGAAAATTCTTTT | 11043 |
rs188061267 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107856091 | GATAACATGACCTTC[A/G]ACTTCTTTCTAGGTA | 11043 |
rs188062301 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | MID2 | GRCh38.p7 | X:107875811 | AGAAGAGAAGGGGCC[C/T]GGATTGGAGAGGAGA | 11043 |
rs188067481 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107906870 | GGATTACAGGCGTGA[A/G]CCACTGCCCTCGGCC | 11043 |
rs188084342 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107910180 | TACCAGCCTCTAGTA[A/G]CCACCATTCTACTCT | 11043 |
rs188086657 | snp | A/G | 0.0220041 | 0.102557 | intron-variant | MID2 | GRCh38.p7 | X:107836473 | GGCCAGGATGGTCTC[A/G]ATCTCCTGACCTTGT | 11043 |
rs188095871 | snp | G/T | 0.00370173 | 0.0428621 | intron-variant | MID2 | GRCh38.p7 | X:107879814 | AGTGATCAGAGATGG[G/T]AAACTATAAACTTTT | 11043 |
rs188247637 | snp | A/G | 0.00633741 | 0.0559334 | intron-variant | MID2 | GRCh38.p7 | X:107868831 | ATTTAAGGGGGATCA[A/G]TCTATGCTTCCATGA | 11043 |
rs188294045 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107924897 | AGCTTAACAAATAGC[A/G]TTTGTTAATTGTTTA | 11043 |
rs188302687 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107837717 | TACTGACCTGTGCTC[C/T]GGGTATGTATGTTTT | 11043 |
rs188310433 | snp | C/T | 0.00528398 | 0.051128 | intron-variant | MID2 | GRCh38.p7 | X:107860366 | GACCTGCAAGGTTTA[C/T]TGTTCTCTGGGTCAG | 11043 |
rs188330227 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107901635 | TCCAGAACTCATGAT[A/G]GAGTGAGGAAGACAG | 11043 |
rs188346038 | snp | C/G | 0.00211696 | 0.0324653 | intron-variant | MID2 | GRCh38.p7 | X:107882958 | AACCAACCCAAATGT[C/G]CATCAATGATAGACT | 11043 |
rs188399825 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | MID2 | GRCh38.p7 | X:107883256 | GCCTAATGTAGGTGA[C/T]GGGTTGATGGGTACA | 11043 |
rs188409693 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107902018 | CACTCAACTGGAGAG[C/G]AGCATATGTGTAAGG | 11043 |
rs188432176 | snp | A/G | 0.000529661 | 0.016265 | utr-variant-3-prime, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107927635 | TATATTCACTTGTGT[A/G]TGTATGTTTATGCAT | 11043 |
rs188490658 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | MID2 | GRCh38.p7 | X:107828567 | TCTGAGGGCCTCGCC[A/G]AGTGCTGGGATTACA | 11043 |
rs188514052 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107864277 | ATCTGTGGTAAGCCT[C/T]TTATGTACTCCTGCC | 11043 |
rs188519499 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107848755 | ACCAGATGGCATGTT[A/C]TGTTGTTGAGAGGCC | 11043 |
rs188548273 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107904867 | TGCTGTGTGTATAAT[A/G]TGAGATGTTTTGAGA | 11043 |
rs188585285 | snp | A/G | 0.00317376 | 0.039709 | intron-variant, nc-transcript-variant | MID2, LOC101928335 | GRCh38.p7 | X:107895543 | AGTATTCTACTATGT[A/G]AATATTCTACAATTT | 11043 |
rs188586603 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107901056 | GGGAGATTAATTAAC[A/G]AGGTTTTTGCAACAA | 11043 |
rs188595984 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | MID2 | GRCh38.p7 | X:107852866 | CTTTTTCAAAAGCAC[A/G]AACTTTGAACTACAA | 11043 |
rs188786990 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107841775 | TATGTGTCGATTTGC[A/G]TATGTAGGTATATGG | 11043 |
rs188821061 | snp | A/G | 0.000529661 | 0.016265 | downstream-variant-500B, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107931907 | TAGAGATTGGAGCAG[A/G]AGTTGAGAATTAAAG | 11043 |
rs188825251 | snp | C/T | 0.0440191 | 0.141675 | intron-variant | MID2 | GRCh38.p7 | X:107886025 | TTCTGGATATTAGCC[C/T]TTTGTTAGATGAGTA | 11043 |
rs188880470 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107875259 | GGTACTTGAGATAGC[A/T]GGGTATACAGATTGG | 11043 |
rs188982245 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | MID2 | GRCh38.p7 | X:107871591 | AACATCCAAGAGGAA[C/T]GAGGTCGCATGAACA | 11043 |
rs188990800 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107829120 | CTGAGCTTAAGGGAT[C/T]CACCTGCCAAGTCCA | 11043 |
rs188994907 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | MID2 | GRCh38.p7 | X:107849341 | GGAGTATGACAAATG[C/G]AGATCATGGTCCAGT | 11043 |
rs189000989 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107914153 | CTTTCTCCTTCATGA[G/T]GTGTGAGCTCTTGAA | 11043 |
rs189012371 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107893093 | TGACTGCTTCAAGAA[C/T]TGGGTGTATCCTCCA | 11043 |
rs189043393 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107831009 | CAGATGCTGAGTTTT[A/C]TTTTAGAAATTCTAT | 11043 |
rs189111092 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107919862 | CCTGTTCTTATACAA[C/T]TGAATGTCTAAAACA | 11043 |
rs189194180 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107914373 | CCTTACTCACCAAAT[C/G]CTGGCTATTCATGTG | 11043 |
rs189221967 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | MID2 | GRCh38.p7 | X:107853796 | AAAACAAAAAAAGTC[A/G]TGGAATACTGCAGCA | 11043 |
rs189226138 | snp | A/C | 0.00422943 | 0.0457911 | intron-variant | MID2 | GRCh38.p7 | X:107876277 | ACTTTCAGGAGATTC[A/C]CTAAAGTACTATCTG | 11043 |
rs189231060 | snp | A/G | 0.00949095 | 0.0682305 | utr-variant-5-prime | MID2 | GRCh38.p7 | X:107822928 | CCATTGCACCCAGCC[A/G]AGATTTGCCATTTTA | 11043 |
rs189235092 | snp | C/T | | | intron-variant | MID2 | GRCh38.p7 | X:107832527 | TATCCTCGTCTGATC[C/T]TCACAATAGCCCGTG | 11043 |
rs189262226 | snp | A/C | 0.00317376 | 0.039709 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107896736 | GCAATGGTTAACTCT[A/C]GAGATTGTGATTGTC | 11043 |
rs189358420 | snp | C/T | 0.00738971 | 0.0603345 | intron-variant | MID2 | GRCh38.p7 | X:107872666 | CCCTCCCAATCTGGG[C/T]TTATAGAGGGAGAAA | 11043 |
rs189377156 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | MID2 | GRCh38.p7 | X:107865768 | CAAAACAATCACTGG[C/T]TTTGGAATAATTTCT | 11043 |
rs189383550 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107897916 | TCTTGATAATTCATC[A/G]GATGTCCAATTTACC | 11043 |
rs189405971 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | MID2 | GRCh38.p7 | X:107892008 | TAACAATGCCCTTTT[C/T]GACCTTAGCTATGAG | 11043 |
rs189438624 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107860937 | TGAATACAGGCACTT[C/T]AGCTCTGGAGCCTGT | 11043 |
rs189468175 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107925656 | ATAACACTCTTTCTG[C/T]TAAAATCTACCCAAA | 11043 |
rs189476748 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107893309 | TTCTTTTTACTGCTA[A/G]ACTATGAAACTATGA | 11043 |
rs189664849 | snp | G/T | 0.00791544 | 0.0624105 | intron-variant | MID2 | GRCh38.p7 | X:107843866 | AAAGGGAGAAAGTTG[G/T]CTGGCAGGAGCTATG | 11043 |
rs189679732 | snp | A/G | 0.00791544 | 0.0624105 | intron-variant | MID2 | GRCh38.p7 | X:107871282 | GTCAGCCACTTCAGT[A/G]CCAGCAGGGGCAGAC | 11043 |
rs189688241 | snp | C/T | | | intron-variant | MID2 | GRCh38.p7 | X:107838754 | GCAAAATTTTCAAGC[C/T]CTGATGAGAGTCTCC | 11043 |
rs189703194 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107912569 | TTGTTTTTGTTTTGT[A/T]TTGCCTTTGTGAGCA | 11043 |
rs189846210 | snp | A/C | 0.0026455 | 0.0362733 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107923763 | CATGAACTGTGATGT[A/C]GTAGAGAGAACACTG | 11043 |
rs189848393 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | MID2 | GRCh38.p7 | X:107861921 | AAAAATGGTATGTAC[A/G]TCCTGGGAGGCAGTG | 11043 |
rs189860793 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107840616 | GTGTATAATTGTGTT[A/G]TATCCATTTTCCTTT | 11043 |
rs189877086 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107903740 | CCAGCCTTCCATTAA[C/T]CATCATGATCTACCA | 11043 |
rs189895271 | snp | A/G | 0.000529661 | 0.016265 | utr-variant-3-prime, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107929302 | TAAACAAAAAAAAAT[A/G]ATTTTTTTCCCCTTC | 11043 |
rs189907446 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | MID2 | GRCh38.p7 | X:107882526 | AAACAAACAACCCCA[C/T]CAAAAAGTGGGCAAA | 11043 |
rs189970813 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107850561 | TGGTGTTTTCATTAG[C/G]CAAAGATTTATTTTT | 11043 |
rs189979117 | snp | A/G | | | intron-variant | MID2 | GRCh38.p7 | X:107830369 | TAGGCCATGGGGCTC[A/G]GCTGCTAGTAGAGGC | 11043 |
rs189995195 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107908159 | TTTTTATTGGCATGA[C/T]CTTACATTTCTAAAT | 11043 |
rs190001864 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107873562 | TAGCCATCCTGGGGA[C/T]TGAAAGATGTATCCC | 11043 |
rs190185039 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107866043 | TATGTGAAAAGGAAG[C/G]AGAAACAATTACACG | 11043 |
rs190213818 | snp | C/T | 0.00011432 | 0.00755955 | missense | MID2 | GRCh38.p7 | X:107854645 | ACCAACCTGGTTAAG[C/T]GCAACAGCGAACTAG | 11043 |
rs190258715 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107897309 | CCCCTTCCCTGGCCA[A/G]AAAAATTACACACTG | 11043 |
rs190344737 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107904342 | TTGGGTGCTTTACTG[C/T]TGTATGTTATAACTC | 11043 |
rs190359120 | snp | C/T | 0.000529661 | 0.016265 | utr-variant-3-prime, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107931176 | AGATGGAGCAATCCA[C/T]GGATGGACTTTTGAA | 11043 |
rs190418930 | snp | A/G | 0.00896606 | 0.0663524 | intron-variant | MID2 | GRCh38.p7 | X:107889748 | TCCCCGTCACTTTCA[A/G]GTACACCAATCAGAC | 11043 |
rs190423174 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | MID2 | GRCh38.p7 | X:107844230 | TAACATGTTCTCAAA[A/G]TGGATTAGAGGGCTT | 11043 |
rs190432698 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | MID2 | GRCh38.p7 | X:107852143 | GTGATCCACCCACCT[C/T]GGTCTCCCAAAGTGC | 11043 |
rs190455374 | snp | A/C/T | | | intron-variant, downstream-variant-500B | MID2, LOC101928335 | GRCh38.p7 | X:107894243 | TACACGAATAGGTAC[A/C/T]GAGAAAGGATATTTG | 11043 |
rs190470705 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107874727 | GACAAACTATTTCAC[C/T]ATACCCAAGTATCCA | 11043 |
rs190481687 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | MID2 | GRCh38.p7 | X:107837123 | AATCCTGACCCATAG[C/T]GTGCTTTCCCAAGCT | 11043 |
rs190484397 | snp | A/G | | | intron-variant | MID2 | GRCh38.p7 | X:107833227 | TAATCGGATGTCAGA[A/G]CTGGAAAGCATCTTA | 11043 |
rs190487008 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107915822 | TGGTATAACTCTTAA[C/T]TGGTTCCTGATGATT | 11043 |
rs190500950 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | MID2 | GRCh38.p7 | X:107878601 | GGACCACCTATTACA[C/T]TGGGGATGGGGTCCA | 11043 |
rs190502103 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | MID2 | GRCh38.p7 | X:107847050 | GATAATGGCCTTCAA[A/G]TTCATGAAAGGTTGA | 11043 |
rs190503075 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107919367 | AAATGAGGGAGTCAA[G/T]GTTGCAGCTTGAGCC | 11043 |
rs190508006 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107898647 | TGAGTCATTTTCATC[A/G]TTATATCCCACTCAG | 11043 |
rs190518331 | snp | C/T | | | intron-variant | MID2 | GRCh38.p7 | X:107857311 | TTTGAGATGGAATCT[C/T]GCTCTGTTGCCCAGG | 11043 |
rs190522442 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107880518 | AGTCGCTTCTGGGTC[A/G]GAGCACATGAGTGAT | 11043 |
rs190524254 | snp | C/T | 0.0068637 | 0.0581785 | utr-variant-5-prime, intron-variant | MID2 | GRCh38.p7 | X:107825896 | GAAGACATGTAAACG[C/T]GCCTCCAGAGGAAGG | 11043 |
rs190532881 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107921776 | GTCAAGATTTAGCCA[C/T]TGGGAGCCTTTCAAG | 11043 |
rs190710101 | snp | A/T | 0.00475684 | 0.0485365 | intron-variant | MID2 | GRCh38.p7 | X:107845899 | ATAAGGGAAAGAAAG[A/T]GAAGTATATTTATGA | 11043 |
rs190718279 | snp | G/T | 0.00422943 | 0.0457911 | intron-variant | MID2 | GRCh38.p7 | X:107859750 | TAAGAGTAGAATTTT[G/T]CCAATAAAAATGAGA | 11043 |
rs190750054 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107890269 | TTCCTTTTGTCTTTG[A/G]TGATGGTGACGTACA | 11043 |
rs190867204 | snp | C/T | 0.00105904 | 0.0229869 | upstream-variant-2KB, utr-variant-5-prime | MID2 | GRCh38.p7 | X:107824032 | TGTTTTCTATTTGCT[C/T]GGATATATATCTAGA | 11043 |
rs190890107 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | MID2 | GRCh38.p7 | X:107867453 | GGCATGAGCCACCGC[A/G]CCCGGCCTGTAGTGT | 11043 |
rs190908186 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107844489 | CATGATATATGGGGC[A/T]TTTCTATAAAACGGC | 11043 |
rs190911738 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107908965 | CTAATTCTAATACCT[G/T]TGTCATATCTGGGTC | 11043 |
rs190922582 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107889906 | TTCTTCCAGTTGATC[A/G]AATCAGCTACTGAGG | 11043 |
rs190964537 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107868524 | TAGGAGAGGACTGAT[C/G]AACTTTCTAGAGAGA | 11043 |
rs190971296 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | MID2 | GRCh38.p7 | X:107824771 | GCCTGTGCTTTAAGT[A/G]TGACTCACTAACTTT | 11043 |
rs190977930 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | MID2 | GRCh38.p7 | X:107829662 | GCCCAGTATTTTGGC[C/T]TCCTGCTTGTTCCAC | 11043 |
rs191002486 | snp | C/T | 0.01368 | 0.0815649 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107909371 | GGGATTGTTCCCTCT[C/T]ATCTTTTTGGGTGGC | 11043 |
rs191057782 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107893624 | GCACTTTTCCAAGTC[C/T]TTTTAAGCAGAATAT | 11043 |
rs191065368 | snp | G/T | 0.00158814 | 0.0281345 | intron-variant | MID2 | GRCh38.p7 | X:107863259 | GTTGAAATACTTGGA[G/T]GGTATTAACACATGA | 11043 |
rs191209005 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | MID2 | GRCh38.p7 | X:107849589 | GATGGCAAAACATTT[C/T]CCTCTTTGGGAAGGG | 11043 |
rs191314200 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107915113 | AATTATTTTTTCACT[A/G]TGTGTCAAATGCTGT | 11043 |
rs191314522 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107843380 | TGGCATCATGAAGCT[A/G]TAGCCCTCATCTCCA | 11043 |
rs191318010 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107841632 | CCTGCAACACCAGTA[A/G]TTCATCCAGGGAAAC | 11043 |
rs191330881 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107888712 | CTAATGTTGACAATG[C/T]GGGGGTGTTAAAGTC | 11043 |
rs191345303 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107905946 | TATATTGATAGGTGC[A/G]TGCTCTTCTCAGTCT | 11043 |
rs191347404 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | MID2 | GRCh38.p7 | X:107865605 | TGATGTTTTCCCCAT[A/G]TAAGGGGAGAAACTG | 11043 |
rs191384184 | snp | A/G | 0.00633741 | 0.0559334 | intron-variant | MID2 | GRCh38.p7 | X:107881798 | AGTACACTTTTTTAT[A/G]TAATCAGGACAATTT | 11043 |
rs191392668 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107835367 | ATTCTTTTGGGTATA[C/T]ACCTAGGAGTGGAAT | 11043 |
rs191400450 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107858580 | TGTGGTGGGCGATTT[A/G]GGGGCTACAAAAGAA | 11043 |
rs191420174 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107899948 | AAAGAAAATACCAGG[A/G]GCTTTCAAATGTCTT | 11043 |
rs191510064 | snp | A/C/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107884161 | ATCCTGGAGTTTATC[A/C/G]GTTGTAAATGATAAA | 11043 |
rs191520602 | snp | A/G | | | intron-variant | MID2 | GRCh38.p7 | X:107840041 | ACTCAGTTTACTAGG[A/G]ATAGAATGGAACGGA | 11043 |
rs191531348 | snp | A/G | 0.000529661 | 0.016265 | utr-variant-3-prime, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107928292 | ATCATTCCTTTTGCA[A/G]TCTTGTTTACAGTAT | 11043 |
rs191536368 | snp | A/T | 0.0440191 | 0.141675 | intron-variant | MID2 | GRCh38.p7 | X:107885655 | AATGGGATGGCTGGG[A/T]CAAATGGTATTTCTA | 11043 |
rs191623802 | snp | C/T | | | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107910830 | TTCCTTTCCTTTCCT[C/T]TCCTTTCCCTCTCTC | 11043 |
rs191763582 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107833619 | AATTGTTAATTAAGT[A/G]GGCATTTAATTATGC | 11043 |
rs191764262 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107830700 | GAAGAGACTAGAAAA[C/G]TGTTTCTCAACTGGT | 11043 |
rs191788682 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107861256 | CATTAGTCATCTTTG[A/G]GGGAGAAGGTTCTAC | 11043 |
rs191801517 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107902600 | TGTCACTCAGCAACA[G/T]ACATATTTTATTTCA | 11043 |
rs191864985 | snp | C/T | 0.00475684 | 0.0485365 | intron-variant | MID2 | GRCh38.p7 | X:107875864 | CCAAAAGGAGGTCCA[C/T]TTTCCTCCCTTTGAT | 11043 |
rs191868954 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107899065 | CTAAGCTGAGGTGAA[A/G]GTGGAAGTGGGGAAG | 11043 |
rs191876465 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107831938 | GTCAATTATCATGTG[C/T]TACCTTGGCAAATCC | 11043 |
rs191876719 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107853252 | AATATGTACCTGAAA[A/G]AATCTATGTACCAGT | 11043 |
rs191877283 | snp | A/G | 0 | 0 | intron-variant | MID2 | GRCh38.p7 | X:107857759 | GAAATGTATAGTAGA[A/G]TACTGTCAGTCATGA | 11043 |
rs191892393 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant, nc-transcript-variant | MID2, LOC101928335 | GRCh38.p7 | X:107895955 | ATGGTTCTGACGAGA[C/T]AGAAAGGAGGTTTCT | 11043 |
rs191925419 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | MID2 | GRCh38.p7 | X:107890579 | TAGGGATCCACTTGA[A/G]GAGGCAGTCTGTCTG | 11043 |
rs191975444 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107896752 | GAGATTGTGATTGTC[A/G]TGAGAGGCAACTCTA | 11043 |
rs191977990 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107918293 | TAGGAACTTCACTCA[C/T]GCCAGTCAAGAGGGG | 11043 |
rs192046835 | snp | A/T | 0.00528398 | 0.051128 | intron-variant | MID2 | GRCh38.p7 | X:107842419 | TTTAAACGGATAGTA[A/T]AATTACCACTCCAAA | 11043 |
rs192141891 | snp | A/T | | | intron-variant | MID2 | GRCh38.p7 | X:107834383 | CAGGTATTTCATCAA[A/T]GCGTTTTTATGACAA | 11043 |
rs192145169 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | MID2 | GRCh38.p7 | X:107877113 | CTGAGATGGCAAACC[A/G]GAGGGCTGAACCAAT | 11043 |
rs192166671 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107881131 | AGATTTTCCTTTACC[A/T]TGCTGTTAGAGTGCT | 11043 |
rs192217945 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | MID2 | GRCh38.p7 | X:107892069 | AATTCCTTGCTCTGT[A/G]TATATACAGGGAGTA | 11043 |
rs192231274 | snp | A/T | | | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107900743 | TCAACTTCCATTTCA[A/T]CCATGCATCTTTCCT | 11043 |
rs192297734 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | MID2 | GRCh38.p7 | X:107891722 | AGAGTTCAGCGTTGG[C/T]TATTATTCTGAGGCT | 11043 |
rs192306988 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | MID2 | GRCh38.p7 | X:107848233 | GAGAAAGAGGGGGAT[A/G]TGTATGAGAGGCAGG | 11043 |
rs192330315 | snp | A/C | | | intron-variant | MID2 | GRCh38.p7 | X:107831486 | CTTAATATATACAGC[A/C]CAGAGATAGAAAAAT | 11043 |
rs192377803 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107827340 | TTGCCTACCCAAATC[C/T]CCCAGCAGAGCCCCT | 11043 |
rs192378238 | snp | A/G | 0.00528398 | 0.051128 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107916457 | ACTCAGGTGACAATT[A/G]GGGAATATTAGAGAA | 11043 |
rs192405722 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107922259 | TTGCTCAATCCCATA[A/G]TACATCTAAAATAGT | 11043 |
rs192524847 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107912430 | CCTTGTTGCTAAATA[C/T]AATAGACACCCCTTT | 11043 |
rs192608075 | snp | C/G | 0.0026455 | 0.0362733 | intron-variant | MID2 | GRCh38.p7 | X:107891135 | TCCTGCACCCTCTTT[C/G]TGAGACTCCCCAGTG | 11043 |
rs192619680 | snp | G/T | 0.00370173 | 0.0428621 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107911310 | TTATGGGACTTTGAT[G/T]AGTGAACTGTTGGAC | 11043 |
rs192622465 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107870398 | TAAGTTGTGTGAGAA[A/T]GATTTGTTCTTTCAA | 11043 |
rs192676888 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | MID2 | GRCh38.p7 | X:107828457 | GTTGGGAACACAGGT[A/G]CATGCCACCACACCC | 11043 |
rs192713515 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | MID2 | GRCh38.p7 | X:107870844 | TCCTTTTCCATTGTT[A/G]GTATTGTATTTTTGT | 11043 |
rs192726309 | snp | A/T | 0.000529661 | 0.016265 | intron-variant, nc-transcript-variant | MID2, LOC101928335 | GRCh38.p7 | X:107895560 | ATATTCTACAATTTG[A/T]TTATATGTGCCCACG | 11043 |
rs192735576 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107853097 | GGGAGAAATAAAAAA[C/G]CCCATGATTAATCTA | 11043 |
rs192892654 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | MID2 | GRCh38.p7 | X:107854092 | TGTGAAAGTAATATG[C/T]GTTCAGTATGCTTCT | 11043 |
rs192899729 | snp | G/T | 0.110232 | 0.207279 | intron-variant | MID2 | GRCh38.p7 | X:107886394 | AATCCTTTCCCCATT[G/T]CTTGTTTTTGTCAGG | 11043 |
rs192927836 | snp | C/T | 0.0230396 | 0.104828 | intron-variant | MID2 | GRCh38.p7 | X:107836493 | CCTGACCTTGTGATC[C/T]GCCTGCCTCAACCTC | 11043 |
rs192935112 | snp | A/C | | | intron-variant | MID2 | GRCh38.p7 | X:107882235 | ACTTAAATGTCAGAC[A/C]TAAAATCATAAAAAC | 11043 |
rs192942337 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107912770 | AGGCTCAGGTATAAC[C/T]TGAGGTGTAGGTGGA | 11043 |
rs192976115 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107917352 | CTTGAGATCCCAGCA[C/T]TTTGCTTCAGGTTGC | 11043 |
rs193089752 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107865099 | ACAGGTGGCAAATTA[A/G]GAGTTTGCATCCAAT | 11043 |
rs193126471 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107859775 | ATGAGATAAGGGAGT[A/G]AAGGGGACCACATGT | 11043 |
rs193131935 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107901202 | AAGAAACCTGTAACT[A/G]TTTGCGATCAGTTGG | 11043 |
rs193146637 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | MID2 | GRCh38.p7 | X:107832566 | AGGGCAGGTATTTTT[C/T]ATCTGATAGATGAAA | 11043 |
rs193153637 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107905414 | CCTTCATGTTGTTTT[C/T]TATTGTTTTTAATTA | 11043 |
rs193162304 | snp | A/G | 0.0131573 | 0.0800346 | intron-variant | MID2 | GRCh38.p7 | X:107859473 | GGTATTAGTGGAGGT[A/G]TAAATGAGCACATTT | 11043 |
rs193279328 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | MID2 | GRCh38.p7 | X:107837242 | GGACAATTTATATGG[C/T]ACCCTCTTAAGCCTT | 11043 |
rs193288078 | snp | C/T | 0.0168099 | 0.0901243 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107925229 | TTCCATGTTCTTAGC[C/T]GCCCCTAGCAGTAAG | 11043 |
rs193288396 | snp | C/T | 0.0440191 | 0.141675 | intron-variant | MID2 | GRCh38.p7 | X:107882555 | AAGGATATGAACAGA[C/T]ACTTCTCAAAAGAAG | 11043 |
rs199506343 | snp | C/T | 0.000529661 | 0.016265 | synonymous-codon, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107916062 | CAATTTTAATGATGC[C/T]TTTGAAAACTTTGCT | 11043 |
rs199533222 | in-del | -/C | 0.0209675 | 0.10022 | intron-variant, nc-transcript-variant | MID2, LOC101928335 | GRCh38.p7 | X:107895221 | ACTTTTTTTGGGGGG[-/C]GGGGTGGATAGTTCT | 11043 |
rs199623265 | snp | G/T | 0.0168099 | 0.0901243 | intron-variant | MID2 | GRCh38.p7 | X:107889221 | TTCCTAGCCTCAATG[G/T]TCTTTACAATTTGGC | 11043 |
rs199651882 | snp | C/T | | | intron-variant | MID2 | GRCh38.p7 | X:107861747 | CAGACTCATAAATGC[C/T]CTGTTTGTGTATTAT | 11043 |
rs199749015 | snp | A/G | | | intron-variant | MID2 | GRCh38.p7 | X:107867600 | GTAGGCACTCAATGT[A/G]TATTTGTTGGATGGA | 11043 |
rs199771473 | snp | G/T | | | missense, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107917724 | AGCTGCTCAAGATTG[G/T]CCGGGGCGCCACGAG | 11043 |
rs199827104 | in-del | -/A | | | intron-variant | MID2 | GRCh38.p7 | X:107833431 | ATATATATATATATT[-/A]TTTTTTAAAAACCTA | 11043 |
rs199835604 | snp | C/G | | | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107906705 | ATTCTCCTGACTTAG[C/G]CTCCCAAGTAGCTGG | 11043 |
rs199836328 | in-del | -/AC | | | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107913062 | CACAGACAGTCAGAT[-/AC]ACACACACACACACC | 11043 |
rs199908428 | in-del | -/C | | | intron-variant | MID2 | GRCh38.p7 | X:107828313 | TTCTTTCTTTTCTTT[-/C]TTTTTTTTTTTTTTT | 11043 |
rs199930811 | in-del | -/TTTA | 0.194455 | 0.243752 | intron-variant | MID2 | GRCh38.p7 | X:107851856 | TATTTCTTTATACTT[-/TTTA]TTTATTTATTTATTT | 11043 |
rs199988289 | in-del | -/A | 0.0068637 | 0.0581785 | intron-variant | MID2 | GRCh38.p7 | X:107880330 | TTTCACCATGTTGCC[-/A]AGGCTGGTCTCGAAT | 11043 |
rs200027408 | snp | A/T | 0.232146 | 0.249362 | intron-variant | MID2 | GRCh38.p7 | X:107845527 | CACACACACACACAC[A/T]CTCTCTCTCTCTCTC | 11043 |
rs200061253 | snp | A/G | 6.86067e-05 | 0.0058565 | missense | MID2 | GRCh38.p7 | X:107854646 | CCAACCTGGTTAAGC[A/G]CAACAGCGAACTAGA | 11043 |
rs200068599 | in-del | -/G | | | intron-variant | MID2 | GRCh38.p7 | X:107888294 | TCTACACACTGCTTT[-/G]AATGTGTCCCAGAGG | 11043 |
rs200088136 | snp | C/T | | | intron-variant | MID2 | GRCh38.p7 | X:107828310 | TTCTTTCTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 11043 |
rs200103358 | snp | A/G | | | intron-variant | MID2 | GRCh38.p7 | X:107880026 | TCTTGTCTGCTGCCC[A/G]GATAGAGCTGACTTA | 11043 |
rs200111395 | in-del | -/T | | | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107903326 | AGTTTTTTTTTTTTT[-/T]CCAACCCTGACTTTG | 11043 |
rs200171254 | snp | A/C | | | intron-variant | MID2 | GRCh38.p7 | X:107885098 | TTTTTTTCCAGGAGA[A/C]TCTCTTATTTATTTA | 11043 |
rs200174235 | in-del | -/G | 0.00738971 | 0.0603345 | intron-variant | MID2 | GRCh38.p7 | X:107845442 | CATATCAGGGATCTT[-/G]TTATAAAATATTACC | 11043 |
rs200198837 | snp | G/T | | | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107907198 | AGAGGTTGGTACTAC[G/T]GCATCACAAATGTAT | 11043 |
rs200199366 | in-del | -/TCA | | | intron-variant | MID2 | GRCh38.p7 | X:107835657 | GCCATTTGTATATCT[-/TCA]TTGGAAAAAATCTAT | 11043 |
rs200206431 | in-del | -/TCAGCT | | | intron-variant | MID2 | GRCh38.p7 | X:107876685 | CCCCAAATCCCTCTG[-/TCAGCT]GCAGAATGGCGTGCT | 11043 |
rs200268274 | snp | A/C | | | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107905458 | TTATCTTATTTTTTT[A/C]TTTTACTAATTCCTT | 11043 |
rs200309928 | snp | A/T | | | intron-variant | MID2 | GRCh38.p7 | X:107851899 | TTTATTTATTTATTT[A/T]TTATTTTTTTGAGAC | 11043 |
rs200475055 | snp | C/T | | | intron-variant | MID2 | GRCh38.p7 | X:107839516 | AGCTGGGACCACAGG[C/T]AAGCGCCACCACGCC | 11043 |
rs200564609 | in-del | -/T | | | intron-variant | MID2 | GRCh38.p7 | X:107833427 | TATATATATATATAT[-/T]ATTTTTTTTAAAAAC | 11043 |
rs200569889 | snp | C/T | 0.000536625 | 0.0163714 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107904072 | GAGACAAAGGTAAAG[C/T]GCAGCACTTCAGTGA | 11043 |
rs200623224 | snp | C/G | | | intron-variant | MID2 | GRCh38.p7 | X:107890312 | GTGTGGATGTCCTTT[C/G]TGTTTATTAGTTTTC | 11043 |
rs200623940 | in-del | -/AACT | | | intron-variant | MID2 | GRCh38.p7 | X:107844739 | CCCAGTGAGCCTCCT[-/AACT]GTCTGCAAAATATAC | 11043 |
rs200642075 | in-del | -/AC | 0.0256233 | 0.11025 | upstream-variant-2KB, utr-variant-5-prime | MID2 | GRCh38.p7 | X:107825719 | ACCATACACACACAC[-/AC]GCACACCCGTCCGGG | 11043 |
rs200685015 | in-del | -/CAGCTA | | | intron-variant | MID2 | GRCh38.p7 | X:107875722 | AACAACAAGTCTCCC[-/CAGCTA]CAACTAAAGAGTTGG | 11043 |
rs200685282 | snp | G/T | | | intron-variant | MID2 | GRCh38.p7 | X:107844604 | TAAAAGAGGCCAAAT[G/T]TCGGTGACTGTCTAT | 11043 |
rs200702692 | snp | C/T | | | intron-variant | MID2 | GRCh38.p7 | X:107874104 | AACTTCTGTCTGTAA[C/T]GAGAATCCAGTTTGG | 11043 |
rs200714821 | snp | A/G | | | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107911123 | CCTCCCAAAGTGCTG[A/G]GATTACAGGTGTGAG | 11043 |
rs200917006 | snp | C/T | 2.3087e-05 | 0.00339749 | stop-gained, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107917736 | TTGGCCGGGGCGCCA[C/T]GAGGCAAGTGTTTGT | 11043 |
rs200944691 | in-del | -/TA | | | intron-variant | MID2 | GRCh38.p7 | X:107833412 | GAAGAATGTTTATTT[-/TA]TATATATATATATAT | 11043 |
rs201041376 | in-del | -/T | | | intron-variant, downstream-variant-500B | MID2, LOC101928335 | GRCh38.p7 | X:107894207 | ATCCTTTTTTTTTTT[-/T]ATACCCAGCACATGG | 11043 |
rs201072364 | in-del | -/T | 0.0183711 | 0.0940641 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107898001 | GCCAAACTCAGCCTC[-/T]TTTTTTCTGTTATGG | 11043 |
rs201112582 | in-del | -/A | 0.0845627 | 0.187431 | intron-variant | MID2 | GRCh38.p7 | X:107882505 | ACTCAAATTTACAAG[-/A]AAAAAAAACAAACAA | 11043 |
rs201130152 | in-del | -/CAGCTG | 0.0709308 | 0.174454 | intron-variant | MID2 | GRCh38.p7 | X:107876686 | CCCAAATCCCTCTGT[-/CAGCTG]CAGAATGGCGTGCTT | 11043 |
rs201133779 | snp | G/T | | | intron-variant | MID2 | GRCh38.p7 | X:107880687 | TGGAATAATGGCAGG[G/T]AATCATTTATGTCTA | 11043 |
rs201188087 | in-del | -/TT | | | utr-variant-5-prime | MID2 | GRCh38.p7 | X:107823387 | TAATATCTGAGATTG[-/TT]TTATATATATATATA | 11043 |
rs201189622 | in-del | -/C | 0.053609 | 0.154695 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107915429 | GGGTGTGGTGGCGGG[-/C]CACCAGCTAGGGAGG | 11043 |
rs201307887 | in-del | -/CT | 0.0440191 | 0.141675 | intron-variant | MID2 | GRCh38.p7 | X:107865545 | GAGGATTGCTTTGAC[-/CT]CTGTTTCCCTCCCCG | 11043 |
rs201321794 | snp | G/T | 0.174253 | 0.238248 | intron-variant | MID2 | GRCh38.p7 | X:107886119 | TGTGCAGAAGCTCTT[G/T]AGTTTAATTAGATCC | 11043 |
rs201343331 | snp | C/G | 0.000529661 | 0.016265 | synonymous-codon | MID2 | GRCh38.p7 | X:107841361 | TCAGGTCGCATCCCT[C/G]AATGATCGATTTGAG | 11043 |
rs201367014 | snp | C/T | | | intron-variant | MID2 | GRCh38.p7 | X:107828312 | CTTTCTTTCTTTTCT[C/T]TTTTTTTTTTTTTTT | 11043 |
rs201426540 | in-del | -/C | | | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107910837 | CCTTTCCTTTCCTTT[-/C]CCTCTCTCTTTCTCC | 11043 |
rs201468127 | in-del | -/CCT | 0.043513 | 0.140937 | intron-variant | MID2 | GRCh38.p7 | X:107894020 | GCTCAGCCTTCACCT[-/CCT]TTAAGAAGCCATCAC | 11043 |
rs201492124 | in-del | -/ACACAC | 0.443677 | 0.15808 | intron-variant | MID2 | GRCh38.p7 | X:107850190 | TCCACACACACACAG[-/ACACAC]ACACACACACACACA | 11043 |
rs201521734 | snp | A/G | 9.14025e-05 | 0.00675965 | missense, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107926141 | CACAAGAAGTTGAAG[A/G]TCTCCAATGATGGAT | 11043 |
rs201658288 | in-del | -/A | | | intron-variant | MID2 | GRCh38.p7 | X:107833429 | TATATATATATATAT[-/A]TTTTTTTTTAAAAAC | 11043 |
rs201686692 | in-del | -/TATG | | | utr-variant-5-prime | MID2 | GRCh38.p7 | X:107823408 | ATATATATATATATA[-/TATG]TATTATCATACAAAT | 11043 |
rs201731263 | in-del | -/T | | | intron-variant | MID2 | GRCh38.p7 | X:107828293 | ACCTCTTTTCTTTTC[-/T]TTTCTTTCTTTCTTT | 11043 |
rs201800936 | in-del | -/T | | | intron-variant | MID2 | GRCh38.p7 | X:107833425 | TTATATATATATATA[-/T]TATATTTTTTTTAAA | 11043 |
rs201868346 | snp | C/T | | | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107911139 | GATTACAGGTGTGAG[C/T]CACCGTGTCTGGCGC | 11043 |
rs201957104 | snp | A/G | 0.000160632 | 0.00896047 | missense, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107924472 | ACCAAGCCGGCAGCC[A/G]GAACAGTGAACCTAC | 11043 |
rs201963071 | snp | A/T | | | intron-variant | MID2 | GRCh38.p7 | X:107851898 | ATTTATTTATTTATT[A/T]ATTATTTTTTTGAGA | 11043 |
rs201969595 | in-del | -/A | 0.0440191 | 0.141675 | intron-variant | MID2 | GRCh38.p7 | X:107869834 | GGCAACCTTATATTT[-/A]AAAAAAAAACCTAGA | 11043 |
rs201979999 | in-del | -/GAGA/GAGAG/GAGC | | | intron-variant, nc-transcript-variant | MID2, LOC101928335 | GRCh38.p7 | X:107894886 | AGAGAGAGAGAGAGA[-/GAGA/GAGAG/GAGC]ACGCCAGTTGAGCAA | 11043 |
rs202031383 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107898903 | GAATTCCTTGCCATA[C/T]AATTATTATTATTAT | 11043 |
rs202050111 | snp | A/G | | | intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107897520 | ATTTAGTCATACTTA[A/G]GTAAAGCTGGAAGGA | 11043 |
rs202069538 | in-del | -/A | 0.043513 | 0.140937 | intron-variant | MID2 | GRCh38.p7 | X:107884683 | AGCTACAAAGAGACC[-/A]AAAAACAAAACAAAA | 11043 |
rs202151467 | snp | A/G | 0.433472 | 0.169818 | intron-variant, nc-transcript-variant | MID2, LOC101928335 | GRCh38.p7 | X:107894867 | TGTGTGTGTGTGTGA[A/G]AGAGAGAGAGAGAGA | 11043 |
rs207478724 | snp | A/C | | | intron-variant | MID2 | GRCh38.p7 | X:107872612 | ACAATGATCTATTCC[A/C]GTGACTTTCAGTGCC | 11043 |
rs267606306 | snp | A/G | | | missense, intron-variant | MID2, LOC101928335 | GRCh38.p7 | X:107926289 | GGGAGGTGGTCATGG[A/G]TTCCTCAACATGGTG | 11043 |
rs367576897 | in-del | -/AA | | | intron-variant | MID2 | GRCh38.p7 | X:107878023 | AAAGGAAAAAAAAAA[-/AA]CAGCTGAAGAGAGGG | 11043 |