| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs7328 | snp | C/T | 0.358303 | 0.225323 | utr-variant-3-prime | GEMIN5 | GRCh38.p7 | 5:154887728 | TGAAAGAGGAGACCC[C/T]TCTCTCTCTACTCTT | 25929 |
| rs15287 | snp | A/T | 0 | 0 | utr-variant-3-prime | GEMIN5 | GRCh38.p7 | 5:154887754 | TTTCaaattaaatat[A/T]ataaaaacaattaaa | 25929 |
| rs168356 | snp | A/G | 0.0807149 | 0.183963 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154924846 | TACAAAAAATTAGCC[A/G]GGCGTGGTGGCGGGC | 25929 |
| rs180902 | snp | A/G | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154913671 | aaaatacaaaaatta[A/G]ccgggtgtggtggtg | 25929 |
| rs180903 | snp | C/T | 0.0810805 | 0.184299 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154913873 | gggcatggtggtatg[C/T]gcctgtagtcccaac | 25929 |
| rs193232 | snp | G/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154913681 | aattagccgggtgtg[G/T]tggtgcacacctgta | 25929 |
| rs348735 | snp | A/C | 0.431029 | 0.17242 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154917235 | CAAATTACAAGTTAC[A/C]ATGCAAATAGTAGCT | 25929 |
| rs348736 | snp | G/T | 0.0807149 | 0.183963 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154917571 | TCAATGGCTGAATTA[G/T]GACTGTGTTACTATG | 25929 |
| rs348737 | snp | A/G | 0.135208 | 0.222087 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154918248 | TACTAAATGTTTACA[A/G]TGCTTAACCTTGTGA | 25929 |
| rs348738 | snp | C/T | 0.0803491 | 0.183626 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154918549 | AGCTCAGACTCCTAG[C/T]ATGAACCTCTGATCC | 25929 |
| rs348739 | snp | A/C | 0.233185 | 0.249445 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154921380 | TGGCCCCCAGGCTAA[A/C]GTATATACAGTCTTC | 25929 |
| rs348740 | snp | G/T | 0.0807149 | 0.183963 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154922180 | ATTTTCTTTTTTTCT[G/T]TTTTAGAGACGGAGT | 25929 |
| rs348741 | snp | A/G | 0.43221 | 0.171171 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154922414 | cctcgtgatctgccc[A/G]cgtcggcctcccaaa | 25929 |
| rs348749 | snp | A/T | 0.301681 | 0.2446 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154937499 | TAGATGTGGCCAGAA[A/T]AAATCACCTGGCATG | 25929 |
| rs348754 | snp | C/T | 0.302184 | 0.244493 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154922985 | acaggcgtgagccac[C/T]gtgccaggccTTAAA | 25929 |
| rs348755 | snp | C/G | 0.126606 | 0.217426 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154924049 | ctcagcccactgaaa[C/G]tattatttaaaatgt | 25929 |
| rs348756 | snp | A/T | 0.0930568 | 0.194599 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154924902 | GCTGAGGCAGGAGAA[A/T]GGCGTGAACCCGGGA | 25929 |
| rs348757 | snp | A/C | 0.289683 | 0.24683 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154924909 | CAGGAGAAAGGCGTG[A/C]ACCCGGGAGGCGGAG | 25929 |
| rs348758 | snp | G/T | 0.108103 | 0.205828 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154925577 | ATGCCATTCCAACAT[G/T]TGGTTATCTTATAAC | 25929 |
| rs702743 | snp | G/T | 0.0807149 | 0.183963 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154891831 | GGGTCTGCTTCTTGG[G/T]TGATAAGAAATAGAA | 25929 |
| rs816734 | snp | A/G | 0.497695 | 0.0338674 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154893387 | ctgtcacccaggctc[A/G]ggtgtagtggcttac | 25929 |
| rs816735 | snp | C/G | 0.299411 | 0.245069 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154893329 | aattcttccgcctca[C/G]cctcccaagtagctg | 25929 |
| rs816736 | snp | C/T | 0.0557983 | 0.157435 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154892388 | AGCCTTTCTCCCTGA[C/T]GGTAAGTGACTTCCT | 25929 |
| rs816737 | snp | C/T | 0.093417 | 0.194889 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154890936 | aaaccccgtctctac[C/T]aaaaattagctgggt | 25929 |
| rs816738 | snp | A/G | 0.0803491 | 0.183626 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154890087 | GGAACCCTTGTGCCT[A/G]TTGGTGGGAATGTAA | 25929 |
| rs816739 | snp | A/G | 0.0561708 | 0.157893 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154889342 | AAATCAGAGAATGGC[A/G]AAATTTCCTGAGAGC | 25929 |
| rs816740 | snp | A/G | 0.0561487 | 0.157866 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154899328 | CAGATTGGCTAAAGG[A/G]TCTGTTCTTGCCTTT | 25929 |
| rs816741 | snp | G/T | 0.0930568 | 0.194599 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154897979 | CCGGAAGGCGGAGGT[G/T]GCAGCGAGCCAAGAT | 25929 |
| rs816742 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154897724 | CAGATGCAGCAGATC[A/G]CTTGAGATTAGGAGT | 25929 |
| rs816743 | snp | C/T | 0.301932 | 0.244547 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154897465 | TGGAAATCTCTTTAT[C/T]TCTTAAATTTTTTTG | 25929 |
| rs816744 | snp | C/T | 0.0807149 | 0.183963 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154897177 | GAATAAAAATGGAGG[C/T]GAAAATAGGACACCC | 25929 |
| rs816745 | snp | A/G | 0.0807149 | 0.183963 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154897113 | ATGACCAAGTCTAGA[A/G]AGATTTTAATTTATC | 25929 |
| rs816746 | snp | C/T | 0.110907 | 0.207733 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154896501 | ATCGCCCCTTTTGTC[C/T]CTTTTCATGCATGAC | 25929 |
| rs816747 | snp | C/T | 0.498547 | 0.0269177 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154896402 | ACACGGGAGAGCTCT[C/T]GAGATCATCCAGTGC | 25929 |
| rs816748 | snp | A/G | 0.0854556 | 0.188216 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154895132 | ATACTTTGAAAAACA[A/G]TTGGACAGTTTCTTT | 25929 |
| rs816749 | snp | G/T | 0.0881222 | 0.190983 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154894519 | cctcccaaagtgctg[G/T]gattacaagtgtgag | 25929 |
| rs863650 | snp | C/T | 0.078151 | 0.181571 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154901656 | ATCAAACAATTGATG[C/T]TTCAGAATGTGTAGA | 25929 |
| rs888694 | snp | G/T | 0.289424 | 0.246872 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154927925 | CAGCTCACTGCAGCC[G/T]CAACCTCCTGGGCTC | 25929 |
| rs903837 | snp | C/T | 0.373196 | 0.217538 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154928303 | AGTGATTCTGAAATT[C/T]AGTTCTGACTTCAGA | 25929 |
| rs1035368 | snp | C/T | 0.333491 | 0.235646 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154928747 | AACAAGCTTTTACAG[C/T]GCAGACTGTGTGTTA | 25929 |
| rs1046337 | snp | A/C | 0 | 0 | utr-variant-3-prime | GEMIN5 | GRCh38.p7 | 5:154887594 | TTATTTGAACAGATC[A/C]CTTACTAAAGCTTTA | 25929 |
| rs1061755 | snp | A/C | | | upstream-variant-2KB | MRPL22, GEMIN5 | GRCh38.p7 | 5:154939341 | ACCTGGAACTGTTTA[A/C]TTTCCTGTAACCATT | 25929 |
| rs1421813 | snp | C/T | 0.174423 | 0.238303 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154902675 | TTCTAAGTGACCTTT[C/T]CCTGTTTGAAAGAGA | 25929 |
| rs1421814 | snp | C/G | 0.165501 | 0.235287 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154902683 | GACCTTTTCCTGTTT[C/G]AAAGAGAGATAATGT | 25929 |
| rs1421815 | snp | A/C | 0.195214 | 0.243923 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154902847 | TGAAGCCCACTTGGT[A/C]ACTGTACACTCCCAC | 25929 |
| rs1974776 | snp | C/T | 0.222813 | 0.248517 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154911936 | AAACAATAGAATAAC[C/T]AGAAAATGTCTTTTC | 25929 |
| rs1974777 | snp | A/G | 0.223487 | 0.24859 | missense | GEMIN5 | GRCh38.p7 | 5:154911849 | ATTTCCGAGGACATC[A/G]AGGTCGACTGCTTTG | 25929 |
| rs2042168 | snp | A/G | 0.302686 | 0.244385 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154906246 | CACTATGGGAGGCCA[A/G]GGAAAGAGACTTGCT | 25929 |
| rs2047305 | snp | A/T | 0.468349 | 0.121752 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154933688 | CAGCTTTATTTATTT[A/T]TTTTTTTTAAAAGAA | 25929 |
| rs2059045 | snp | C/T | 0.0807149 | 0.183963 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154910479 | catttctaccaagaa[C/T]tgcaaaataaaagca | 25929 |
| rs2112222 | snp | C/T | 0.084364 | 0.187256 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154933769 | AGCTTGATCTGTTGG[C/T]GATTAGGTTGCATAA | 25929 |
| rs2112223 | snp | C/T | 0.289424 | 0.246872 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154929415 | TCCCCACCCACAGCA[C/T]GTTCACTGCCAAATT | 25929 |
| rs2161128 | snp | C/G | 0.302686 | 0.244385 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154933864 | GATAGAGAGGATGAA[C/G]AGAAAGGTGGTAGGC | 25929 |
| rs2258437 | snp | C/T | 0.223481 | 0.24859 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154927412 | TGATGTAGAAAGTAA[C/T]AGCTGTTTGTCATCC | 25929 |
| rs2270622 | snp | A/G/T | 0.024134 | 0.107647 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154920190 | ACCATACCATACTAC[A/G/T]TAGTTGTTTTAAAAG | 25929 |
| rs2544863 | snp | A/G | | | | | GRCh38.p7 | 5:154893254 | tttttttttttttta[A/G]agacgggctttcacc | 25929 |
| rs2544866 | snp | A/G | 0.301932 | 0.244547 | | | GRCh38.p7 | 5:154932016 | CATTTTTTATTTATT[A/G]TTTATTTTTGGAGAC | 25929 |
| rs2544870 | snp | C/T | 0.0325976 | 0.123435 | | | GRCh38.p7 | 5:154913437 | tgtataatttgaata[C/T]agtcatgagaaaata | 25929 |
| rs2644742 | snp | C/G | 0.493013 | 0.058691 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154914202 | ATTTTTGTATTTTTA[C/G]TAGAGACAGGGTTTC | 25929 |
| rs2644743 | snp | C/T | 0.333491 | 0.235646 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154928722 | CATGCATGAAGTCAC[C/T]GGTGGTTCATAACAC | 25929 |
| rs2644744 | snp | C/T | 0.289683 | 0.24683 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154931675 | AACTTAGCTATCTCT[C/T]TCATAGGTCTGAACT | 25929 |
| rs2644745 | snp | C/T | 0.0810805 | 0.184299 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154934293 | ctgggttcaagtgat[C/T]ctcctgcctcagcct | 25929 |
| rs2688185 | snp | A/T | 0.0930568 | 0.194599 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154903671 | TCTTTTGAATTTTTG[A/T]ACTGTTTTGTCTGTA | 25929 |
| rs3749672 | snp | C/T | 0.000230624 | 0.0107359 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154932166 | CCATGATGATGAAAT[C/T]CACTCCATAGCCTGG | 25929 |
| rs4354100 | snp | C/T | 0.299411 | 0.245069 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154911032 | cagttgtcccagatt[C/T]ggtcagtgggaacct | 25929 |
| rs4958393 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154908608 | tttgactttcataat[C/T]tgaaacttctgaaga | 25929 |
| rs4958769 | snp | C/T | 0.0807149 | 0.183963 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154907078 | TGAGAGCCATCACTA[C/T]AGCTTAACTCACTAG | 25929 |
| rs4958770 | snp | A/C | 0.0964687 | 0.197302 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154907309 | CTATGTACACAACTG[A/C]CCCAGCTTCGCTTCG | 25929 |
| rs4958771 | snp | A/G | 0.299158 | 0.245119 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154932751 | TATTTTTTTGTAGAG[A/G]TGAGGTTTCACCATG | 25929 |
| rs6580117 | snp | A/G | 0.0807149 | 0.183963 | downstream-variant-500B | GEMIN5 | GRCh38.p7 | 5:154887108 | CTCACTGTCCCAACA[A/G]CTCCAATCCTAGGAA | 25929 |
| rs6580118 | snp | A/G | 0.30839 | 0.243086 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154905143 | AGTTTGTAGTGAGCC[A/G]AGAGTGTGCCACTGC | 25929 |
| rs6580119 | snp | C/T | 0.0503378 | 0.150449 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154907555 | TCCCAGACACGACCA[C/T]GAAATCCTAGTGATA | 25929 |
| rs6580120 | snp | A/G | 0.288646 | 0.246995 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154909533 | TACACCAATTTTTAA[A/G]TACTTTGGTACAAAG | 25929 |
| rs6580121 | snp | A/G | 0.0930568 | 0.194599 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154911659 | ATGTCTTCCTTGCTC[A/G]ATCCTGATCAACTCA | 25929 |
| rs6580122 | snp | C/T | 0.498547 | 0.0269177 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154924771 | GAGGCGGGCGGATCA[C/T]GAGGTCAGGAGATCG | 25929 |
| rs6860198 | snp | C/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154909130 | tgcctgggtaatttt[C/T]gtatttttttttttt | 25929 |
| rs6865950 | snp | A/G | 0.17154 | 0.237369 | missense | GEMIN5 | GRCh38.p7 | 5:154896226 | CCCTCTCCACGAAAG[A/G]CCCTTCGGTGCCCGT | 25929 |
| rs6879093 | snp | A/G | 0.0930568 | 0.194599 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154908866 | ctgtttaactactaa[A/G]tatttgcatctacta | 25929 |
| rs6879277 | snp | C/T | 0.299411 | 0.245069 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154909107 | gggactacaggtgtg[C/T]gacaccatgcctggg | 25929 |
| rs7379585 | snp | C/T | 0.0807149 | 0.183963 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154894141 | ctagagacaggtttt[C/T]gccatgttgcccagg | 25929 |
| rs7381141 | snp | A/G | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154907457 | ACTTGAATAAAGCTT[A/G]ACAAAAAAAACTAAT | 25929 |
| rs7709899 | snp | A/G | 0.221439 | 0.248363 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154901853 | GGCTCAGGCTGGAGC[A/G]CAGTAGCACAATAAT | 25929 |
| rs7720521 | snp | A/G | 0.0807149 | 0.183963 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154904104 | CAAATTTTTTTCTAA[A/G]AAAATGCCATATTAT | 25929 |
| rs7720538 | snp | C/T | 0.0807149 | 0.183963 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154904100 | CCATCAAATTTTTTT[C/T]TAAAAAAATGCCATA | 25929 |
| rs7726729 | snp | A/G | 0.245631 | 0.249962 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154928234 | ACACTTGAAGTGACT[A/G]AAGCTCAGAAAAGTA | 25929 |
| rs7733367 | snp | C/G | 0.093417 | 0.194889 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154893903 | agcccgccaccacgc[C/G]cggctaaCACCGATA | 25929 |
| rs10037626 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154908888 | catctactagttttt[C/G]tattcactgatgttt | 25929 |
| rs10042134 | snp | C/T | 0.0930568 | 0.194599 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154911101 | GAATTCTTTGAGTAC[C/T]GCCTTCCTTTCTGGC | 25929 |
| rs10064509 | snp | A/C | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154907459 | TTGAATAAAGCTTAA[A/C]AAAAAAAACTAATGC | 25929 |
| rs10075074 | snp | G/T | 0 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154888836 | AGCTAACCAAAGTAA[G/T]TGGATTCTAAAttct | 25929 |
| rs10477107 | snp | A/G | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154908202 | ttttttttttttgga[A/G]atggtttcgctcttc | 25929 |
| rs10515726 | snp | C/T | 0.414576 | 0.188188 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154902991 | CTAACCATTATAATA[C/T]CACAGGATGACAGCC | 25929 |
| rs10522124 | in-del | -/AGTGAGCCAAGATCCCGCCATTGCACTCCAGCCTGGGCGACAGAGCCAGACTCCGTCTCAAAAAAAAAAAAAAAAGTAATTAATA | 0 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154936358 | GGAGGCGGAGCTTGC[lengthTooLong]CTTATTAGTAGTACT | 25929 |
| rs10629944 | in-del | -/TC/TTC | 0.0995161 | 0.199636 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154901795 | GTGCTTTTTTTTTTT[-/TC/TTC]CCCTTTCCTTTTATT | 25929 |
| rs10714011 | in-del | -/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154897903 | GGGCTGACTAAGGTG[-/T]TTTTTTTTGTGTTTT | 25929 |
| rs11167703 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154901163 | AGACTCCGTCTCTAC[A/G]AAAAACTAAAAAATT | 25929 |
| rs11167705 | snp | G/T | 0.498568 | 0.0267188 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154911191 | CTCCAAGAAGCCATG[G/T]ACATTTTTAGTGGAG | 25929 |
| rs11281580 | in-del | -/CCAAACT/TCCAAAC | 0 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154900886 | CAAAATGTAGGAGGT[-/CCAAACT/TCCAAAC]AATTCTAGAATATGA | 25929 |
| rs11283455 | in-del | -/TCCAAAC | 0.0807149 | 0.183963 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154900885 | TCAAAATGTAGGAGG[-/TCCAAAC]TAATTCTAGAATATG | 25929 |
| rs11285608 | in-del | -/A | 0.11963 | 0.213316 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154899620 | ATGTGCTTTTTTATT[-/A]AAAAAAAAAAAATGT | 25929 |
| rs11743080 | snp | C/T | 0.372995 | 0.217652 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154906208 | cctatgttgcttagg[C/T]tagtctcaagctcct | 25929 |
| rs11952692 | snp | C/G | 0.0930568 | 0.194599 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154910794 | agctccgcctcctgg[C/G]ttcacgccattctcc | 25929 |
| rs12186480 | snp | C/T | 0.200492 | 0.245049 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154922357 | TACTTTTAGTAGAGA[C/T]GGGGTTTCACAGTGT | 25929 |
| rs12186885 | snp | C/T | 0.444444 | 0.157135 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154908172 | TTTTACCCAGATGTC[C/T]TTTTTTTTTTTTTTT | 25929 |
| rs12187974 | snp | A/T | 0.153 | 0.230415 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154903835 | AAAATTAAAAAAAAA[A/T]TTTTTTTTTTAAATA | 25929 |
| rs12188149 | snp | G/T | 0.195214 | 0.243923 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154910193 | ttggattgttaccag[G/T]ttttggtgatcacag | 25929 |
| rs12332539 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154915103 | TAATAATCATAAGGA[C/T]CAGAATCAGCTTTCT | 25929 |
| rs12658626 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154928071 | TTATTATATACTTTC[A/G]TTCTTCTTGAACCAT | 25929 |
| rs13155370 | snp | G/T | 0 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154921757 | GTATTCACTTTACGG[G/T]CATGTAAAAGATGAG | 25929 |
| rs13156153 | snp | G/T | 0.299916 | 0.244966 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154922220 | TCACCCAGGCTGGAG[G/T]GCAGTGGTGCAATCT | 25929 |
| rs13177143 | snp | C/T | 0.110167 | 0.207236 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154918794 | CATGCCTATAATCAG[C/T]ACTTTGGGAGGCCAA | 25929 |
| rs13177245 | snp | G/T | 0.5 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154904908 | CCCAAAATGGAAGTG[G/T]AAGTctgggcacaat | 25929 |
| rs13177484 | snp | G/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154888870 | TTTTTGTTTTGTTTT[G/T]TTTTTGAGACAGAGT | 25929 |
| rs13181649 | snp | C/T | 0.0807149 | 0.183963 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154911456 | AGGTGGAGGCTGCAG[C/T]GAGCCAAGATCACGC | 25929 |
| rs13182236 | snp | A/G | 0.136566 | 0.222784 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154935794 | GAAAATGCAAAACAC[A/G]ATCATAAACAAACAA | 25929 |
| rs13186258 | snp | C/T | 0.0655868 | 0.168795 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154932991 | CACTCTAGACCTGCA[C/T]ATTCCAAGGCTGTCA | 25929 |
| rs17562321 | snp | A/G | 0.0832709 | 0.186283 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154921911 | TTTGAAGGTTGTTGT[A/G]GTAATGATATGTGAT | 25929 |
| rs17647858 | snp | C/T | 0.0212378 | 0.100837 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154931629 | TTAAACACGCACTAA[C/T]ATAAAAAAATTAGTT | 25929 |
| rs34021306 | in-del | -/GTTTT/TTTTGT/TTTTT | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154888865 | TTTTTTTTTGTTTTG[-/GTTTT/TTTTGT/TTTTT]TTTTTTTTTTGAGAC | 25929 |
| rs34031330 | snp | C/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154932506 | TACTATGTATGTTGC[C/T]TGGTACAAAACTCAC | 25929 |
| rs34185329 | snp | A/G | 0.000247221 | 0.0111153 | missense | GEMIN5 | GRCh38.p7 | 5:154896232 | TGGAACACGGGCACC[A/G]AAGGGCCTTTCGTGG | 25929 |
| rs34227223 | snp | A/G | 0.000234341 | 0.010822 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154917011 | TTACGTGCACAACCT[A/G]AAGACTGTCATAGGT | 25929 |
| rs34285700 | in-del | -/C | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154920527 | GTCATCAAAGCAGTG[-/C]ATTTCCTTAGTATCA | 25929 |
| rs34492229 | in-del | -/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154910775 | CAATCTCGGCTCACT[-/T]GCAAGCTCCGCCTCC | 25929 |
| rs34791646 | snp | C/T | 0.0062894 | 0.0557238 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154902603 | AGGAGATCTCAAAGG[C/T]GTTCTCCAGACTGCA | 25929 |
| rs34795441 | in-del | -/C | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154918931 | TGTAATCCCAGCTAC[-/C]TCAGGTGGCTGAGAC | 25929 |
| rs34855620 | in-del | -/T | 0 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154891076 | TTTTTTTTTTTTTTT[-/T]GTAGAGACAGGGTCT | 25929 |
| rs34871845 | in-del | -/G | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154893906 | CGCCACCACGCCCGG[-/G]CTAACACCGATATTA | 25929 |
| rs35194608 | snp | A/G | 0.00781046 | 0.0620018 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154891327 | ACACCAAAAGAGTCA[A/G]CTCTGTAAATCCACA | 25929 |
| rs35229651 | in-del | -/T | | | frameshift-variant | GEMIN5 | GRCh38.p7 | 5:154904520 | CCTCTGGAGTGCTTT[-/T]GCAGTTGCTAGTACC | 25929 |
| rs35280009 | in-del | -/A | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154915894 | TTTTCTATACAAAAA[-/A]TTATTCATTCATGTT | 25929 |
| rs35359985 | snp | C/T | 0.00437347 | 0.0465576 | missense | GEMIN5 | GRCh38.p7 | 5:154937111 | CCTGGTCAGTACAAC[C/T]TCTGTGCCACCAGCT | 25929 |
| rs35454029 | in-del | -/C | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154905646 | AGGAGTAGTTTCCCC[-/C]TTTCCCACCTCCCAA | 25929 |
| rs35458616 | in-del | -/T | 0 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154897931 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCCCAC | 25929 |
| rs35522740 | snp | C/G | 0.0391159 | 0.134293 | missense | GEMIN5 | GRCh38.p7 | 5:154927510 | ACTCAATCTTGGAGA[C/G]GGAAATACACCCTCT | 25929 |
| rs35557414 | in-del | -/G | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154897583 | CCTCTGCCTCCTGGG[-/G]TTCAAGCAATTCTCC | 25929 |
| rs35562111 | snp | G/T | 0.00787514 | 0.0622539 | missense | GEMIN5 | GRCh38.p7 | 5:154891677 | CCAGCTTTCAAAAGT[G/T]TGGAGGCCTTTTTTC | 25929 |
| rs35678751 | in-del | -/T | | | frameshift-variant | GEMIN5 | GRCh38.p7 | 5:154918001 | GTGTACAGGCAATTT[-/T]GTACTAGAAAGCAAA | 25929 |
| rs35707071 | snp | A/G | 0.00144861 | 0.0268739 | missense | GEMIN5 | GRCh38.p7 | 5:154891455 | CTCACAGAAGAAGGT[A/G]AGCGAATGCTGAGTA | 25929 |
| rs35713011 | in-del | -/G | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154926978 | GGCGTAAAACTGGGG[-/G]AGGTGGAGCTTGCAG | 25929 |
| rs35726896 | in-del | -/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154919650 | TGAAAAGGATGCTTT[-/T]ATACATAACACCTGA | 25929 |
| rs35770974 | in-del | -/TC | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154901796 | TGCTTTTTTTTTTTC[-/TC]CCTTTCCTTTTATTG | 25929 |
| rs35813730 | in-del | -/G | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154912723 | AAAAAAAAACCCAGT[-/G]CTTAGCCTAGGCCCT | 25929 |
| rs35861034 | in-del | -/C | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154922319 | CTACAGGCACCTGCC[-/C]ACCAAGCCCGGCTAA | 25929 |
| rs35899504 | snp | A/G | 0.000576972 | 0.0169751 | missense | GEMIN5 | GRCh38.p7 | 5:154898477 | CCAACAACTGGGTGG[A/G]AGCCCAGGAAGCCCT | 25929 |
| rs35913543 | in-del | -/CCT | 0 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154922806 | GGTTCAAGCAATTCT[-/CCT]ACCTCAGCCTCCCGA | 25929 |
| rs35963276 | in-del | -/A | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154922248 | CTCCGCTCACTGCAA[-/A]GCTCCGCCTCCTGGG | 25929 |
| rs35995081 | in-del | -/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154930408 | GAAAGTTTTATATTT[-/T]GAGTGCTATTTCTTT | 25929 |
| rs55647433 | in-del | -/GTTTT/GTTTTT | 0 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154888869 | TTTTTGTTTTGTTTT[-/GTTTT/GTTTTT]TTTTTTGAGACAGAG | 25929 |
| rs55847218 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154903636 | AGACACAAGAAACTG[A/G]TAATAGTTTGATTAT | 25929 |
| rs56187116 | snp | G/T | 0.0872718 | 0.189788 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154933349 | TTTTTCACTCATTCT[G/T]TTTGTAATTCATCCA | 25929 |
| rs56773390 | snp | C/T | 0.17332 | 0.23795 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154891977 | TCATTCAAAGCATGA[C/T]AGAGTATTCCATTTG | 25929 |
| rs56895891 | snp | A/T | 0.202035 | 0.245356 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154916052 | GGTAACTGTTTTTTT[A/T]TTAATTTTTATTTTT | 25929 |
| rs57097969 | snp | A/G | | | missense | GEMIN5 | GRCh38.p7 | 5:154891253 | TACCACTGGCTCTGA[A/G]AACTGCAGAGGGGCT | 25929 |
| rs58672004 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154906271 | ATAGTGCTGGGATTA[C/T]AGGCATGAACCACCA | 25929 |
| rs58812410 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154935468 | GCCGCATCACTTTCC[C/T]AATCTAAAGGGAGCG | 25929 |
| rs60191789 | in-del | -/A | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154927052 | CAGAAAAAAAAAAAA[-/A]CACTAACACTAACAA | 25929 |
| rs60467186 | in-del | -/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154916819 | TCTGTTACCATTTTT[-/T]GTCATGTTTGAAAGA | 25929 |
| rs60625540 | in-del | -/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154905716 | TTTTTTTTTTTTTTT[-/T]GAGACGAAGTCTCAC | 25929 |
| rs60715487 | in-del | -/A | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154921485 | AGGCATAATGAAAAA[-/A]CAGACCATCTTTTTC | 25929 |
| rs61038340 | in-del | -/CATTA | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154895679 | GTTGATGGGTTATTA[-/CATTA]TTCTGCTTTTCTATA | 25929 |
| rs61749642 | snp | C/T | 0.00405779 | 0.0448601 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154899193 | TCCTCAGGCTTACCA[C/T]TTGGCAGCTACAGCA | 25929 |
| rs61749643 | snp | A/G | 0.00905033 | 0.0666578 | missense | GEMIN5 | GRCh38.p7 | 5:154899279 | CTGGGTCCTCCGGGC[A/G]CAGCCGGGCCTTGGC | 25929 |
| rs61749644 | snp | C/T | 0.00511404 | 0.0503077 | missense | GEMIN5 | GRCh38.p7 | 5:154905368 | AGATACCAACCTGGC[C/T]TCTCTTTTGGTGGCT | 25929 |
| rs61754586 | snp | A/G | | | missense | GEMIN5 | GRCh38.p7 | 5:154891631 | CAAGGTCTGGAGAGA[A/G]ACCACCAGAATTCAT | 25929 |
| rs61758976 | snp | A/G | 0.0203218 | 0.0987316 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154920021 | AAAGGCTTCTCCACT[A/G]AGCTTCCAGGGATTA | 25929 |
| rs62382193 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154894797 | CTGTAATCCCAGCTA[C/T]CCGGGAGGCTGAGGC | 25929 |
| rs62382194 | snp | C/G | 0.0955749 | 0.196603 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154903515 | CTGAGTAATTTTCCA[C/G]TAAGGAAAATAATGT | 25929 |
| rs62382195 | snp | A/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154903848 | AATTTTTTTTTTTAA[A/T]TAGAGAGAGGGTCTC | 25929 |
| rs62382196 | snp | G/T | 0.5 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154926545 | TTGGGAGAAAATGAA[G/T]TCTACCAAATAAGCC | 25929 |
| rs62382237 | snp | C/T | 0.5 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154933457 | GTTTATTCATTTTCC[C/T]TTTGAAGGGCTTCCA | 25929 |
| rs66512779 | in-del | -/ACC | 0.296619 | 0.245615 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154909554 | TGGTACAAAGTACCT[-/ACC]ACCACCACAATTACT | 25929 |
| rs66537820 | in-del | -/A | 0 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154914528 | AAAAAAAAAAAAAAA[-/A]GTAAAATAGTGTAAT | 25929 |
| rs66578685 | in-del | -/CTC | 0.299664 | 0.245017 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154922804 | TGGGTTCAAGCAATT[-/CTC]CTACCTCAGCCTCCC | 25929 |
| rs68045388 | in-del | -/ATTAC | 0.299158 | 0.245119 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154895675 | TCTGGTTGATGGGTT[-/ATTAC]ATTATTCTGCTTTTC | 25929 |
| rs70981957 | in-del | -/T | 0 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154893280 | ACCAAGCCCGGCTAA[-/T]TTTTTTTTTTTTTTT | 25929 |
| rs70981958 | in-del | -/A | 0 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154909134 | AAACCCCATCTCTAC[-/A]AAAAAAAAAAAAAAA | 25929 |
| rs71577161 | in-del | -/G | 0.5 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154910510 | GATCTCGCTCTGTTG[-/G]CCAGGCTGGTCTCAA | 25929 |
| rs71597673 | snp | A/C | 0.5 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154930585 | TAAGTGAAATAAGCC[A/C]ATCACAAAAAGACAT | 25929 |
| rs72799513 | snp | C/T | 0.0966517 | 0.197444 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154909620 | TTGTAGTAAGATATA[C/T]CCCCTGCTTGAGCCC | 25929 |
| rs73278861 | snp | A/T | 0.5 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154895657 | ATGTGAACATCTGTT[A/T]ATTCTGGTTGATGGG | 25929 |
| rs73278885 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154911418 | CTAGGGAGGTCAAGG[C/T]GCGAGAATTGCTTTA | 25929 |
| rs73807206 | snp | G/T | 0.221141 | 0.248329 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154926352 | TCTCCAAGTTCGGTG[G/T]TCTTTCTGTCCTATT | 25929 |
| rs73807207 | snp | A/G | 0.193653 | 0.243567 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154929958 | AATGTCCATCAGTGT[A/G]TGAGATATGAGTTCT | 25929 |
| rs73809503 | snp | C/G | 0.0256215 | 0.110247 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154897440 | TTACTGATTTTTAAT[C/G]AGATGGGAACAAAAA | 25929 |
| rs73809507 | snp | A/T | 0.195214 | 0.243923 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154923609 | CTTACAGACACTGAA[A/T]TCTGAATTTTATTTA | 25929 |
| rs74360948 | snp | A/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154909133 | CTGGGTAATTTTTGT[A/T]TTTTTTTTTTTTTTT | 25929 |
| rs74403237 | snp | A/C | 0.5 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154932410 | TAATTTTGCTTTTTC[A/C]TTTTTTTAAAGTGCT | 25929 |
| rs74408508 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154910343 | TTTCACAGAGACAGT[A/G]TCCCCCTATGTTGTC | 25929 |
| rs74428468 | snp | A/T | 0 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154914528 | TTTTTTTTTTTTTTT[A/T]AAAGAGACTAGGTCT | 25929 |
| rs74635634 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154900844 | GAGTTTTGATTTGTT[G/T]AATGCATAAGGCATT | 25929 |
| rs74699442 | snp | A/C | 0.5 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154893088 | AGCATGAGAGTGAGA[A/C]TCCCTCTCAAAACAA | 25929 |
| rs74794389 | snp | A/G | 0.247053 | 0.249983 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154901856 | TCAGGCTGGAGCGCA[A/G]TAGCACAATAATGGC | 25929 |
| rs74803058 | snp | A/G | 0.00431899 | 0.0462692 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154901508 | AAATAAAAGATGGTG[A/G]TTAAAAAAACAGTTG | 25929 |
| rs74807599 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154932443 | CCTTATGCCTCCTGG[G/T]TTTGTTAAAACCCTT | 25929 |
| rs74850514 | in-del | -/AAAT | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154925129 | ACAATTGAAAAAAAC[-/AAAT]GAGTTCAAATACGTA | 25929 |
| rs74913459 | snp | A/C | 0.5 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154917525 | CATTAATGACAAATG[A/C]TGATAGGGAGAAGCT | 25929 |
| rs75084477 | snp | G/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154905700 | AAGTCTATTACTTTG[G/T]TTTTTTTTTTTTTTT | 25929 |
| rs75088494 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154929442 | GGGAGTACCTCCACC[C/T]GACATGCTTCTAATC | 25929 |
| rs75108487 | snp | A/C | 0.0217236 | 0.101931 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154929785 | TACTATTAGTTACCT[A/C]CCACTGATGAAGCCT | 25929 |
| rs75123260 | snp | A/C | 0.152001 | 0.229992 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154896451 | TTGTATCTGCAGCAA[A/C]CAAAGCACATTAGTG | 25929 |
| rs75241060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154916638 | GACTAAAGGCATGCA[C/T]CTCTAACCCGGCAAA | 25929 |
| rs75462033 | in-del | -/AAA | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154894918 | TCTAAAAAAAAAAAA[-/AAA]GTAAAAATATTAGCT | 25929 |
| rs75462135 | snp | C/T | 0.5 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154888849 | AATTGGATTCTAAAT[C/T]CTTTTTTTTTGTTTT | 25929 |
| rs75661665 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154894421 | TTCATTGTTTTAGTG[A/G]AATATCTAGGTAGCA | 25929 |
| rs75704487 | snp | C/T | 0.221141 | 0.248329 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154926766 | TACACTAACACTAGG[C/T]CAGGCGCCGTGGCTC | 25929 |
| rs75723710 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154928787 | ACTTAGAATTCAGAT[A/C]TCATTTTCCAATGGT | 25929 |
| rs75815361 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154898934 | CCTTTATTTGATGTT[A/G]TAAGAGACCATTAGA | 25929 |
| rs75836689 | snp | G/T | 0.5 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154890483 | TTTTTTTTTTTTTTT[G/T]TTGTAGAGACAGGGT | 25929 |
| rs75869039 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154896470 | AGCACATTAGTGAGC[C/T]ACCTGCCCCATATGA | 25929 |
| rs75898562 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154900839 | CATCTGAGTTTTGAT[G/T]TGTTGAATGCATAAG | 25929 |
| rs75922491 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154935533 | CACCTGGGAGTTCAT[A/G]TTGTATCAACGGGCA | 25929 |
| rs76116236 | snp | G/T | 0 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154909151 | TTTTTTTTTTTTTTT[G/T]TTTGTAGAGATGGGG | 25929 |
| rs76147653 | snp | A/G | 0.5 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154909982 | AGACTCCGTTTCAAG[A/G]AAAAAAAAAAAGAAT | 25929 |
| rs76192856 | snp | A/C | 0.0032066 | 0.0399126 | missense | GEMIN5 | GRCh38.p7 | 5:154889392 | TTAACTCAGGCAGAG[A/C]AAGTGGCTCATTTTT | 25929 |
| rs76296548 | in-del | -/CAGTGAGCCAAGATCCCGCCATTGCACTCCAGCCTGGGCGACAGAGCCAGACTCCGTCTCAAAAAAAAAAAAAAAAGTAATTAATA | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154936357 | AGGAGGCGGAGCTTG[lengthTooLong]CTTATTAGTAGTACT | 25929 |
| rs76463319 | in-del | -/TGA | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154925132 | ATTGAAAAAAACAAA[-/TGA]GTTCAAATACGTAAA | 25929 |
| rs76509445 | snp | C/T | 0.200492 | 0.245049 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154932829 | GTTGGCCTCCTAAAG[C/T]GATGGGATTATAGGC | 25929 |
| rs76530344 | snp | C/T | 0.00115892 | 0.0240441 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154907592 | ATTCTGCCACATACC[C/T]GCTGGAGCAAGGCCA | 25929 |
| rs76551019 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154917562 | ATTAACAGATCAATG[A/G]CTGAATTATGACTGT | 25929 |
| rs76633515 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154932986 | TTCTACACTCTAGAC[C/T]TGCATATTCCAAGGC | 25929 |
| rs76740941 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154925660 | TAGAAAAAATGCTGA[A/G]ATGAACAGAGCCTTA | 25929 |
| rs76813157 | in-del | -/GAAAAAAAA/GAAAAAAAAA | 0.0869089 | 0.189476 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154907456 | ACTTGAATAAAGCTT[-/GAAAAAAAA/GAAAAAAAAA]AACAAAAAAAACTAA | 25929 |
| rs76818494 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154915912 | ATTCATTCATGTTCA[C/T]GAAGATCTATGTATA | 25929 |
| rs76880515 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154892035 | AACAGATCACACTGT[C/G]TCTCTGAAAAATCAC | 25929 |
| rs77015526 | snp | A/T | 0.5 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154914025 | AATAAATACACACAT[A/T]ATTTTTTTTTTTTTG | 25929 |
| rs77128270 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154937594 | TCTTACAGTAAGGAA[C/T]GCCACACGTTGCAGG | 25929 |
| rs77182184 | snp | A/G | 0 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154925129 | ACAATTGAAAAAAAC[A/G]AATGAGTTCAAATAC | 25929 |
| rs77214035 | snp | A/C/T | 0.00478244 | 0.0486902 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154933273 | TTCCTAAATAAGATA[A/C/T]AGATTTTGCATATTT | 25929 |
| rs77215386 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154889545 | CCATTTAAAAATACA[C/T]AGTTCAGTGATTTTA | 25929 |
| rs77226340 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154895521 | GAGCTAGGGAAGGAG[G/T]GAAGGGCTGAGGAAA | 25929 |
| rs77315862 | in-del | -/AAAACTA | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154907471 | AACAAAAAAAACTAA[-/AAAACTA]TGCTGTTTCCAAGAG | 25929 |
| rs77502360 | snp | A/G | 0.178785 | 0.239642 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154890459 | GTCACCTGGCTTCTT[A/G]AAATTTAATTTTTTT | 25929 |
| rs77600469 | snp | G/T | 0.5 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154934033 | ATTGACTTTTTTTTT[G/T]GAGATAGAGTCTTGC | 25929 |
| rs77711671 | snp | C/T | 0.000873283 | 0.0208777 | missense | GEMIN5 | GRCh38.p7 | 5:154898571 | TGGCAGCCAACTCTG[C/T]AGCCGTTCTAAGTGA | 25929 |
| rs77715664 | snp | C/T | 0.0654984 | 0.168698 | upstream-variant-2KB | GEMIN5 | GRCh38.p7 | 5:154938413 | GCCTGAGCACAGCCC[C/T]GAGGTTAAGCATTCT | 25929 |
| rs77761603 | snp | A/T | 0.00914312 | 0.0669923 | utr-variant-3-prime | GEMIN5 | GRCh38.p7 | 5:154887540 | TCAATCCATTTGTTA[A/T]AAAACTGAAGGGAAA | 25929 |
| rs77953901 | snp | C/T | 0.0670745 | 0.170406 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154907330 | CTTCGCTTCGTCCCA[C/T]GGTTTTACCTTGCCC | 25929 |
| rs78137514 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154934659 | CCGTCTCCTTCTCCC[C/T]CTCCCTCAAGAGTAC | 25929 |
| rs78292025 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154904756 | AAGCTCCTCCTCCTA[A/G]TAAAGAGGCTTTCAA | 25929 |
| rs79179035 | snp | C/G | 0.0654984 | 0.168698 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154918666 | AATTAAAGACAATGA[C/G]GGAATATAATCAACA | 25929 |
| rs79221580 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154909254 | ATTACAGGCGTGAGC[C/T]ACTGTGCCTGGCCCA | 25929 |
| rs79263531 | snp | G/T | 0.5 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154914532 | TTTTTTTTTTTTAAA[G/T]AGACTAGGTCTTACC | 25929 |
| rs79402925 | snp | C/G | | | missense | GEMIN5 | GRCh38.p7 | 5:154896107 | CTGTTTGGCAGGTGT[C/G]TTATTTGTAGCAGAT | 25929 |
| rs79406353 | snp | C/T | 0.5 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154895586 | TTTATTTTATAAAGT[C/T]CTCAAATCAAAATAC | 25929 |
| rs79406849 | snp | A/G | 0.5 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154914530 | TTTTTTTTTTTTTTA[A/G]AGAGACTAGGTCTTA | 25929 |
| rs79411329 | snp | A/G | 0.151668 | 0.229849 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154900138 | GTGCCTGAGTTTCCC[A/G]TAAGTTAGAATTTTC | 25929 |
| rs79547055 | snp | A/C | 0.5 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154924920 | CGTGAACCCGGGAGG[A/C]GGAGCTTGCAGTGAG | 25929 |
| rs79672310 | snp | C/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154901795 | CGTGCTTTTTTTTTT[C/T]CCCTTTCCTTTTATT | 25929 |
| rs79714774 | snp | A/T | 0.5 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154914028 | AAATACACACATAAT[A/T]TTTTTTTTTTTGAGA | 25929 |
| rs79878825 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154935032 | CATCTGAATCCAATC[C/T]CCTCTTGACTTTTCA | 25929 |
| rs79982665 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154926319 | ACACAATTAATAAAC[C/G]AGAACCCACGCCTCC | 25929 |
| rs80098147 | snp | A/T | 0.5 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154914027 | TAAATACACACATAA[A/T]TTTTTTTTTTTTGAG | 25929 |
| rs80222919 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154937884 | GTTTCCCTAGCTGTA[A/G]AAAACGGGGTGGAGT | 25929 |
| rs111326319 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154893249 | CCCGAGGTGAAAGCC[C/T]GTCTCTAAAAAAAAA | 25929 |
| rs111328655 | snp | A/G | 0.5 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154899116 | ACCTCTAAACTTATT[A/G]CTTGTATTCTTGTCC | 25929 |
| rs111333229 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154910997 | GCCATCGCACCTGGC[C/T]TCCTCTTACTTATGT | 25929 |
| rs111392481 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154933242 | TTATATCATTCCTAG[C/T]CTTTCTTTGTATATA | 25929 |
| rs111396162 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154934604 | GGTGTGAGCCACTGC[A/G]CCCAGCCTTATCATC | 25929 |
| rs111398051 | snp | A/G | 0.5 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154926351 | GTCTCCAAGTTCGGT[A/G]GTCTTTCTGTCCTAT | 25929 |
| rs111414840 | snp | C/T | 0.5 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154902986 | TAAAACTAACCATTA[C/T]AATATCACAGGATGA | 25929 |
| rs111511808 | snp | A/G | 0.5 | 0 | missense | GEMIN5 | GRCh38.p7 | 5:154911759 | TGATCTTGCATGGAA[A/G]TGAGCCACTTGTGCA | 25929 |
| rs111605705 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154894321 | TTCATCAGTTGATGG[A/G]CATTTGGGTTGTTTC | 25929 |
| rs111655923 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154892032 | GACAACAGATCACAC[C/T]GTCTCTCTGAAAAAT | 25929 |
| rs111722966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154918097 | CCTAGAGTTTAAAAA[C/T]GTTTTAATTATACAA | 25929 |
| rs111724572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154931338 | GAAGCAGAATTCTAG[A/G]CCAAAAAGTGAAGAA | 25929 |
| rs111745769 | snp | C/T | 0.5 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154927158 | CCCTGGGCAAAACTA[C/T]CCTTCTTTATTATGT | 25929 |
| rs111811979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154917739 | TACTCTCAATGGGCT[A/G]AAAATATCTAAATAA | 25929 |
| rs111896074 | snp | C/G | 0 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154894078 | GCCACCCTAGTACCT[C/G]GGATTACAGGCTTGT | 25929 |
| rs111942169 | snp | A/C | 0.5 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154898767 | CCTTCCTGTGGTCCC[A/C]GGTATGTCACTGCCC | 25929 |
| rs111955529 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154934165 | GGCTTACAGGTGTGC[A/G]CCACCAAGTCTGGCT | 25929 |
| rs112076278 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154912490 | ATCTGGCTTGGCATT[G/T]CATCTTTATTTATTT | 25929 |
| rs112106696 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154917767 | TAATTCTGTAGTTCT[C/T]AAAGACACAAGGCAC | 25929 |
| rs112136505 | snp | C/G | 0.5 | 0 | utr-variant-5-prime | GEMIN5 | GRCh38.p7 | 5:154938214 | TAGGGAGCGGGGCGG[C/G]GTGAACTCCGAGCCC | 25929 |
| rs112145889 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154920219 | AGAACTATATATTTG[A/C]AACATTCTAATACAT | 25929 |
| rs112206460 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154921663 | ACTACCAAAACGATT[A/T]AGTCCCAAACATATT | 25929 |
| rs112213511 | snp | C/T | 0 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154909656 | AATCACTAATTTGCT[C/T]TCACTGTGGTTTAGT | 25929 |
| rs112300664 | snp | A/G/T | 0.000181657 | 0.00952886 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154921353 | CTTACCAAGTGACAT[A/G/T]GGGGGTACTGGTGGC | 25929 |
| rs112320535 | snp | G/T | 0.0221141 | 0.102801 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154910912 | ACCTGTTAGTCAGGA[G/T]GGTCTCGGATCTCCC | 25929 |
| rs112323495 | snp | C/T | 0.00100475 | 0.0223912 | missense | GEMIN5 | GRCh38.p7 | 5:154889331 | CTTACCTTAATGCTC[C/T]CAGGAAATTTCGCCA | 25929 |
| rs112376134 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154907838 | AAGAATCACAATAAA[A/G]GACTGACTAAAGTAT | 25929 |
| rs112379969 | snp | G/T | 0.5 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154911401 | ACCTGTAGTCCCAGC[G/T]ACTAGGGAGGTCAAG | 25929 |
| rs112384346 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154927819 | CAACAAAGTGAGACC[A/G]TCCCTACAAACAATT | 25929 |
| rs112530144 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154913957 | CATGAGCTATAACTG[C/T]ACCACTACACTCCAC | 25929 |
| rs112531797 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154904396 | GAGAACATAAAAATA[C/T]AGAAAACAATTTAGA | 25929 |
| rs112557283 | snp | C/G | 0 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154906569 | TTTGTGAAAGAAAGA[C/G]TTTTTAAAAAAAAGA | 25929 |
| rs112606926 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154935620 | AGGAGTTAGATCCGA[A/G]AAACGAAGAAAGTAC | 25929 |
| rs112624361 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154936652 | ACGCATTTACAGTCT[A/G]TATCAGGAGTCCATT | 25929 |
| rs112705865 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154929837 | GCTACTTGCTTTACA[C/T]GCATTTGGGCAAATA | 25929 |
| rs112749432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154907880 | TAAAAGCACTCTAGG[C/T]GGTAAACTCCAATAT | 25929 |
| rs112867779 | in-del | -/G | 0.5 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154919909 | TTTATTTTGCAAGAT[-/G]GGGAAACACAGAGGG | 25929 |
| rs112868953 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154920717 | TAAATCTACTTATCC[C/T]CTCTATGTAATGCAA | 25929 |
| rs112880270 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154911481 | TCACGCCACTACATT[C/T]CAGTCTGGGCAACAG | 25929 |
| rs112942279 | in-del | -/T | 0.5 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154905701 | AGTCTATTACTTTGG[-/T]TTTTTTTTTTTTTTT | 25929 |
| rs112955504 | snp | C/T | 0.5 | 0 | missense | GEMIN5 | GRCh38.p7 | 5:154917956 | TGCCAAGAGCCATGA[C/T]TTTGCCATCTGCTTT | 25929 |
| rs112996026 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154916688 | TTTTTGTAGAGACGG[A/T]GCCTCACTATTTAAC | 25929 |
| rs113005028 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154898127 | GCTTGTCTCAAACTC[C/T]TGACCTCAAGTGATC | 25929 |
| rs113086106 | snp | A/G | 0.0146672 | 0.084371 | upstream-variant-2KB | MRPL22, GEMIN5 | GRCh38.p7 | 5:154939536 | AGGAAGGGGCTGCCA[A/G]TGAAAGAGCCAAGAT | 25929 |
| rs113092116 | in-del | -/A | 0.5 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154927991 | GCAAGACCCTGTTTC[-/A]AAAAAAAAAAAAAAT | 25929 |
| rs113109187 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154935306 | ATTTCTCCTTCAACA[C/T]TCTAGGGAAATTGCT | 25929 |
| rs113148762 | snp | A/G | 0.5 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154898153 | TGATCTGCCTGCCTC[A/G]GCCTCCCAAAGTGCT | 25929 |
| rs113234818 | in-del | -/TTTTG | 0.0539704 | 0.155153 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154888855 | TTCTAAATTCTTTTT[-/TTTTG]TTTTGTTTTGTTTTT | 25929 |
| rs113256940 | snp | A/G | 0.5 | 0 | missense | GEMIN5 | GRCh38.p7 | 5:154892429 | CCTGCATGATGGTGA[A/G]GCTCCCTGAGTCATA | 25929 |
| rs113283625 | snp | G/T | 0.5 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154921645 | TATCAAATAATGACA[G/T]TTACTACCAAAACGA | 25929 |
| rs113366984 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154907957 | TGAACTTTTAGAATT[A/G]TATTATCACAATATT | 25929 |
| rs113442614 | in-del | -/A | 0.419296 | 0.183954 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154909981 | AGACTCCGTTTCAAG[-/A]AAAAAAAAAAAAGAA | 25929 |
| rs113478516 | snp | C/T | 0.245346 | 0.249957 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154893037 | GGAAGGTGGAGGTTG[C/T]GGTGAGCTGAGATTG | 25929 |
| rs113559969 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154901948 | GGGGACTACAGGTAC[A/G]TGTCACCATGCCCAG | 25929 |
| rs113637815 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154914904 | ACAACACATTAAAAA[C/T]TGTTGAATCTATTAA | 25929 |
| rs113641096 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154905259 | TATTTTGAACCTATA[A/C]AAACAAACAAGAAAC | 25929 |
| rs113757164 | snp | C/T | 0.5 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154899034 | TCAGGAAGTAGTTCC[C/T]GATGAGTCTTATGAA | 25929 |
| rs113785684 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154919785 | CTCTTTGTTTTATTC[A/G]AGGATAAAGACTCCT | 25929 |
| rs113951006 | snp | C/T | 0.5 | 0 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154893977 | TGAGACAGGGTCTCA[C/T]TCTCTTACCCAGGCT | 25929 |
| rs113971212 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154910624 | TTAATATATTTTGTC[C/T]AGCTTTCTAGTTGCT | 25929 |
| rs114146651 | snp | A/G | 0.000399281 | 0.0141238 | missense | GEMIN5 | GRCh38.p7 | 5:154932123 | CCTCTTGGTTTATAG[A/G]TAAACAATCTTCACC | 25929 |
| rs114154166 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154930259 | AGCTGATAGGGGAAC[A/G]ACACAGCAGCAGGGG | 25929 |
| rs114154734 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154890614 | GACTACAAGTGCATG[C/T]CACCACTACTGGCTA | 25929 |
| rs114205951 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154937393 | TCTCTGAGCCTCAGC[C/T]TCTCAACTGTGAAAT | 25929 |
| rs114209008 | snp | C/T | 0.000477598 | 0.0154457 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154896122 | GTTATTTGTAGCAGA[C/T]GGGTACTTGATGTTC | 25929 |
| rs114231281 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154897410 | GTTTTGATGTGTCAA[A/G]AAGGCAGTGGTATGT | 25929 |
| rs114254512 | snp | A/T | 0.0209421 | 0.100162 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154914586 | TGACAGTCATATAGC[A/T]AACTGTAGCCTCCAA | 25929 |
| rs114422435 | snp | A/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154895727 | TTATTTTACTTTTTT[A/T]GAAAAGGAAATAGTG | 25929 |
| rs114584785 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154920281 | CACAGTTGTTGGGAG[C/T]AGAAGTAAAAAAACT | 25929 |
| rs114704610 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154905557 | TGTAAAAATTAAGAG[A/C]CATTCCAAGCTTAGC | 25929 |
| rs114951927 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154930196 | TTACCCCGGCACTCT[A/C]TTTAAATCAGCGAAT | 25929 |
| rs115094055 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154895785 | TCACAGCTCTTAGGA[A/G]TCTGAGGCGGGAGAA | 25929 |
| rs115228276 | snp | G/T | 0.00400476 | 0.0445684 | missense | GEMIN5 | GRCh38.p7 | 5:154921417 | TATGTGCTAGAAATC[G/T]GTGGAGGCCTTTAGA | 25929 |
| rs115282394 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154933163 | CAATCAAACCTCTCT[C/T]CTTGCCAGATCTCTT | 25929 |
| rs115321488 | snp | A/G | 0.000495131 | 0.0157264 | missense | GEMIN5 | GRCh38.p7 | 5:154917051 | TTGTTGGAGCCAGAG[A/G]CCATCAGATAGCTCA | 25929 |
| rs115326955 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154909827 | CTACTAAAAACACAA[A/G]CAATTAGCTGGGTGT | 25929 |
| rs115339026 | snp | C/T | 0.0031859 | 0.0397844 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154891786 | CATGCATTTCTCTAG[C/T]TGCCAGAAATGTGGC | 25929 |
| rs115339287 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154911421 | GGGAGGTCAAGGTGC[A/G]AGAATTGCTTTAACC | 25929 |
| rs115374618 | snp | A/C | 0.150333 | 0.229274 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154910323 | TAAAATAAAAAAAAA[A/C]CTTATTTCACAGAGA | 25929 |
| rs115551140 | snp | A/G | 0.0125027 | 0.0780706 | missense | GEMIN5 | GRCh38.p7 | 5:154898591 | GTTCTAAGTGATGCC[A/G]CATCCCCCTTTTTGG | 25929 |
| rs115749014 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154930258 | TAGCTGATAGGGGAA[C/G]GACACAGCAGCAGGG | 25929 |
| rs115893184 | snp | A/G | 0.000890046 | 0.0210768 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154896242 | CCCTTCGGTGCCCGT[A/G]TTCCAAGTGTGGTAA | 25929 |
| rs116063578 | snp | C/T | 0.021333 | 0.101051 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154916230 | TAGATCCTTGTGTAC[C/T]GACATAAAAAGATGT | 25929 |
| rs116096944 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154909849 | GCTGGGTGTGAGGCA[C/T]GCACCTATAGTCACA | 25929 |
| rs116106895 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154921741 | TTATCACCACCCAAA[G/T]GTATTCACTTTACGG | 25929 |
| rs116322096 | snp | A/T | 0.00398564 | 0.0444627 | utr-variant-3-prime | GEMIN5 | GRCh38.p7 | 5:154887577 | ATTTGAATCACTTCT[A/T]CTAAAGCTTTAGTAA | 25929 |
| rs116322935 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154934706 | CAAACCTGGCTGAAT[C/T]CAACCATCTCCTTTC | 25929 |
| rs116337360 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154916666 | AAATTTGTTTTTTAT[C/T]TTCAATTTTTTGTAG | 25929 |
| rs116395207 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154906568 | TTTTGTGAAAGAAAG[A/G]CTTTTTAAAAAAAAG | 25929 |
| rs116422219 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154919619 | CCACAGCATCACTTT[C/G]GTGAAAGTGGTTGGC | 25929 |
| rs116577037 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154895937 | TTAAAGGGCTTTGAT[C/T]AGTCTAAAGGGATCT | 25929 |
| rs116579476 | snp | C/T | 0.00188246 | 0.0306217 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154899274 | CAGGACTGGGTCCTC[C/T]GGGCGCAGCCGGGCC | 25929 |
| rs116664700 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154901946 | GCGGGGACTACAGGT[A/G]CATGTCACCATGCCC | 25929 |
| rs116821443 | snp | A/G | 0.0018952 | 0.0307247 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154917098 | ATGCTCATGATGCCA[A/G]CTAATGGTATTCACA | 25929 |
| rs117153755 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154930188 | CAAACCACTTACCCC[A/G]GCACTCTCTTTAAAT | 25929 |
| rs118134227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154937891 | TAGCTGTAGAAAACG[A/G]GGTGGAGTCGTCCAC | 25929 |
| rs137886608 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154899829 | GAAGAACATTTTGTG[C/T]TCTCTGCTGCATTCC | 25929 |
| rs138046123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154905142 | GAGTTTGTAGTGAGC[C/T]AAGAGTGTGCCACTG | 25929 |
| rs138241147 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154915749 | ACGGGAATGAGGTAT[A/G]TGTCCTCTGTTTGTG | 25929 |
| rs138249132 | snp | C/T | 8.24355e-05 | 0.00641957 | missense | GEMIN5 | GRCh38.p7 | 5:154898481 | CTTCCTGGGCTCCCA[C/T]CCAGTTGTTGGCCAG | 25929 |
| rs138345102 | snp | C/G | 0.000313115 | 0.0125084 | missense | GEMIN5 | GRCh38.p7 | 5:154920039 | CTTCCAGGGATTATG[C/G]TGTAAGACAATCCCT | 25929 |
| rs138453329 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154935508 | AGAGAGACCCAGCAA[A/G]GTCATCTGACACCTG | 25929 |
| rs138472694 | in-del | -/CCAAACT | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154900880 | AGATATCAAAATGTA[-/CCAAACT]GGAGGTAATTCTAGA | 25929 |
| rs138495755 | snp | A/C | 1.64762e-05 | 0.00287016 | missense | GEMIN5 | GRCh38.p7 | 5:154925941 | AGTGTATTCCATACA[A/C]GGATCATGCCATCCC | 25929 |
| rs138498500 | snp | C/T | 0.021333 | 0.101051 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154888900 | TCTCGCTCTGTTGCC[C/T]AGGCTGGAGTGCAGT | 25929 |
| rs138700526 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154900963 | GCTGATACACAACTT[C/T]ACTACTTACCAAAAC | 25929 |
| rs138715829 | snp | A/G | 0.000282244 | 0.0118761 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154917023 | CTTCAGGTTGTGCAC[A/G]TAAATGACTGCATTG | 25929 |
| rs138724004 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154906196 | AGATGGGGGTTCCCT[A/G]TGTTGCTTAGGCTAG | 25929 |
| rs138761088 | snp | G/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154897914 | GGTGTTTTTTTTTGT[G/T]TTTTTTTTTTTTTTT | 25929 |
| rs138770378 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime | GEMIN5 | GRCh38.p7 | 5:154888028 | CACAATTGAGTCTAA[A/C]GTCAGATCCACCGTT | 25929 |
| rs138773390 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154904092 | AAAAGCTTCCATCAA[A/T]TTTTTTTCTAAAAAA | 25929 |
| rs138779297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154910399 | CAAGCCATCCTCCTG[C/T]CTCGGCATCCCAAAG | 25929 |
| rs138793902 | snp | A/G | 4.9423e-05 | 0.00497082 | missense | GEMIN5 | GRCh38.p7 | 5:154902650 | GGTGAAATAACTCAG[A/G]GTGGCCATTTTCTAA | 25929 |
| rs138826310 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154910878 | TAATTTTTTGTATTT[G/T]TAGTAGAGACAGGGT | 25929 |
| rs138828203 | snp | C/T | 0.00106526 | 0.0230542 | missense | GEMIN5 | GRCh38.p7 | 5:154896303 | TTTTCCTCCAGATGC[C/T]TGGACAGTAGCTCCA | 25929 |
| rs138908258 | snp | A/G | 1.64749e-05 | 0.00287005 | missense | GEMIN5 | GRCh38.p7 | 5:154904599 | CTCAGGGGAAGCAAG[A/G]AACGAGCTTTTCTCT | 25929 |
| rs138987708 | snp | C/T | 0.00010226 | 0.00714979 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154891705 | TGGTGTGGCAGGGGA[C/T]TGATGGTCCCCCAAC | 25929 |
| rs138992297 | snp | A/G | 0.202035 | 0.245356 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154924858 | GCCAGGCGTGGTGGC[A/G]GGCGCCTGTAGTCCC | 25929 |
| rs139038065 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154930788 | TGTACACTTAAAAGT[A/G]ATAAAGATGGCAAAT | 25929 |
| rs139044743 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154914036 | ACATAATTTTTTTTT[A/T]TTTGAGATGGAGTTT | 25929 |
| rs139067075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154890299 | ATTGGATTATCTTTT[A/G]TTATGCCTGGGTAGC | 25929 |
| rs139092018 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154919599 | CTATATTATTGTTAT[C/T]TTTACCACAGCATCA | 25929 |
| rs139175889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154895836 | GCGGCTGCAGTGAGC[C/T]AAGATCATGCCACTG | 25929 |
| rs139179892 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154923377 | AAGAGCGAAACTCTG[A/T]CTCCAAAAAAAAAAG | 25929 |
| rs139196921 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154921239 | AGCCCACATAAGCAG[A/T]CAGTGCACTAGACCA | 25929 |
| rs139237130 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154926387 | CACTGGTAACCCCCT[C/T]ATTTGGCAAACTCTA | 25929 |
| rs139330071 | snp | A/G/T | 0.000153988 | 0.00877328 | missense | GEMIN5 | GRCh38.p7 | 5:154931518 | TTCCAGTGGCTAAGT[A/G/T]GCAACCTTTTGTTAC | 25929 |
| rs139368576 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154908654 | TTTGTCCAATTTCCC[C/T]CAATTTAGGTCTGCC | 25929 |
| rs139530101 | snp | A/G | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154901927 | CACCACAGCCTCCCG[A/G]GTAGCGGGGACTACA | 25929 |
| rs139532385 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154917679 | TCAACATAGGAGGTG[A/G]CCATTTTGTGAGGGA | 25929 |
| rs139620582 | snp | C/T | 0.0162398 | 0.0886349 | upstream-variant-2KB | MRPL22, GEMIN5 | GRCh38.p7 | 5:154939155 | CGCCACACTTTGAGA[C/T]GAATTAAGAGTCCAT | 25929 |
| rs139639865 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154896868 | GAAGCACAGAGAAGG[C/T]CTAGAAAATCTACTT | 25929 |
| rs139679779 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154937482 | TGAAAGTGACTCTTA[C/T]TTAGATGTGGCCAGA | 25929 |
| rs139793527 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154932816 | GCAATCTACCTGCGT[C/T]GGCCTCCTAAAGTGA | 25929 |
| rs139832608 | in-del | -/TTAT | 0.195214 | 0.243923 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154915895 | TTTTCTATACAAAAA[-/TTAT]TCATTCATGTTCACG | 25929 |
| rs139885199 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154933404 | CTGGCCAGTCATTAC[A/G]CTATTGTATTAGTAC | 25929 |
| rs139967968 | snp | C/T | 3.31873e-05 | 0.0040734 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154927538 | AGTGAGATCCCATTG[C/T]AACAGTTCACCTCTG | 25929 |
| rs140074592 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154902378 | TGCTTTTTTTCAAAG[G/T]GGTTGGGTTGGATTT | 25929 |
| rs140096627 | snp | A/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154906656 | CCTGCCTCAGCCTCC[A/T]GAGGATCTGGGACTA | 25929 |
| rs140256959 | snp | C/T | 9.89511e-05 | 0.00703319 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154905424 | ATTAATGGTGACTTT[C/T]GACTTTTCAAAGCCT | 25929 |
| rs140322037 | snp | C/T | 0.000280503 | 0.0118395 | missense | GEMIN5 | GRCh38.p7 | 5:154899231 | CATCTCTTTCTAGGA[C/T]GGTTCCCCAGCTGAG | 25929 |
| rs140327693 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154914792 | TGTGTATATTTTAAG[A/G]GAAAGATTAAACTAT | 25929 |
| rs140347499 | snp | C/T | 1.64811e-05 | 0.00287059 | missense | GEMIN5 | GRCh38.p7 | 5:154917961 | AGAGCCATGATTTTG[C/T]CATCTGCTTTCCAAC | 25929 |
| rs140400209 | in-del | -/CT | 0.222928 | 0.24853 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154933840 | TCTGAAGATCCTCCC[-/CT]GACTCCTGCCTACCA | 25929 |
| rs140416900 | snp | A/C | 1.65217e-05 | 0.00287412 | missense | GEMIN5 | GRCh38.p7 | 5:154901433 | CATACTGATCCTGAA[A/C]ACACAGCTGTTTGGC | 25929 |
| rs140492898 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154892292 | GCTGGCCAATCTCCA[A/T]CTTTTAAGAATCTAG | 25929 |
| rs140599853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154898786 | ATGTCACTGCCCCGG[C/T]TGTTCCTGTGAAGGC | 25929 |
| rs140636657 | snp | A/G | 0.000165226 | 0.00908768 | missense | GEMIN5 | GRCh38.p7 | 5:154911739 | GACCTTGAGGAGGCC[A/G]GGAATGATCTTGCAT | 25929 |
| rs140648327 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154891004 | CAAGTGATCTGCCCA[C/T]CTCGGCCTCCCAAAG | 25929 |
| rs140649913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154934643 | AAAATACCCGTACGC[C/T]CCGTCTCCTTCTCCC | 25929 |
| rs140830060 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154909868 | CCTATAGTCACAGCT[A/T]CTCAAAAGGCTGAGG | 25929 |
| rs140936760 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154916219 | TAACAGCAAGATAGA[A/T]CCTTGTGTACTGACA | 25929 |
| rs140946196 | snp | A/C | 3.31923e-05 | 0.0040737 | splice-donor-variant | GEMIN5 | GRCh38.p7 | 5:154924467 | AATCACCCATTTCTT[A/C]CTTGTTGGAGTAGGT | 25929 |
| rs141006294 | snp | A/G | 0.00318978 | 0.0398085 | downstream-variant-500B | GEMIN5 | GRCh38.p7 | 5:154887310 | ACTGTTTAAATAACC[A/G]AGGAGGAGAAAAAAA | 25929 |
| rs141010715 | snp | A/G | 0.0125621 | 0.0782513 | missense | GEMIN5 | GRCh38.p7 | 5:154896280 | AGCTTTTGCCCTCTG[A/G]AAGCTGCTTTTCCTC | 25929 |
| rs141025447 | snp | A/G | 0.000675871 | 0.0183706 | missense | GEMIN5 | GRCh38.p7 | 5:154907786 | CCTTAGGTTGAGAGA[A/G]CCGTTTTTTCTCCAA | 25929 |
| rs141048056 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154912727 | AAAAAACCCAGTCTT[A/G]GCCTAGGCCCTATGT | 25929 |
| rs141131049 | snp | A/T | 0.221141 | 0.248329 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154889143 | AGCCTCCCAAAGCGC[A/T]GGGATTACAGGCGTG | 25929 |
| rs141353470 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154898386 | TGGATTTGACTAGAA[A/G]AGGATTTGGGACACT | 25929 |
| rs141416457 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154915262 | TACACATAGGATTCT[C/T]AGAAAACTACTGAAG | 25929 |
| rs141426030 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154928455 | GGCCATTACTTTCTC[C/T]ATCCTAGGAGGACTT | 25929 |
| rs141457910 | snp | C/T | 1.64855e-05 | 0.00287097 | missense | GEMIN5 | GRCh38.p7 | 5:154889365 | TCTGATTTGCCTCGG[C/T]AAGCCTTTTGGTTAA | 25929 |
| rs141607329 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154931745 | TTCGGCCTGGTGCAG[C/T]GGCTCACGCCTGTAA | 25929 |
| rs141629991 | snp | C/T | 0.000247135 | 0.0111134 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154927478 | TGAATGATTTTGCCC[C/T]TCTGATGAGGCACTG | 25929 |
| rs141631321 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154923683 | ACTTAAAAAGCAAAA[A/C]CATTCTTAATTCATG | 25929 |
| rs141774971 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154901676 | AATTGTTTGATTATG[G/T]AACACAAACAAAACA | 25929 |
| rs141832132 | snp | A/G | 0.000216953 | 0.0104129 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154938032 | GACAAGGAAGACGGA[A/G]GTCCGCGCGGCGAAG | 25929 |
| rs141837144 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154910531 | CTGGTCTCAAACTCC[C/T]GGCCTCAAGTGATCC | 25929 |
| rs141889049 | snp | G/T | 0.000280004 | 0.0118289 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154928577 | GCTGGGCCAATGGAG[G/T]GTCAACCAAAGGCGC | 25929 |
| rs141897922 | snp | A/C | 3.30224e-05 | 0.00406326 | missense | GEMIN5 | GRCh38.p7 | 5:154925876 | CCGCTGTAACCTTGG[A/C]CTTCACGCCTTGCCA | 25929 |
| rs141928097 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154924688 | ATTTAAAGGAGAAAA[A/C]GGGTATTAAAAACAA | 25929 |
| rs141969729 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154903667 | GCAATACAGACAAAA[C/T]AGTTCAAAAATTCAA | 25929 |
| rs141972048 | snp | C/T | 0.00392375 | 0.0441189 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154911854 | CAGTCGACCTCGATG[C/T]CCTCGGAAATTGCAC | 25929 |
| rs142030424 | snp | A/G | 3.29457e-05 | 0.00405854 | missense | GEMIN5 | GRCh38.p7 | 5:154904551 | AAACAGTCCTGATGA[A/G]GCTCCTCTTTGGATC | 25929 |
| rs142095826 | snp | A/T | 3.32358e-05 | 0.00407637 | missense | GEMIN5 | GRCh38.p7 | 5:154891664 | AGACGCCCATAAAGA[A/T]AAAAGGCCTCCAAAC | 25929 |
| rs142138063 | in-del | -/A | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154926220 | GAAAGCACTGCTAAG[-/A]AAAAAAAAATAGTAA | 25929 |
| rs142217294 | snp | C/G | 0.000462512 | 0.0152001 | missense | GEMIN5 | GRCh38.p7 | 5:154898445 | ACAGACTGACCTGTA[C/G]ACTTTCATGCAGCTG | 25929 |
| rs142230460 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154931032 | TGATTGAGGGGCTCT[A/G]TAATTTGGATAAAAT | 25929 |
| rs142252259 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154892182 | GTGGAAAGTGGACAG[A/G]AGGCTGTAAGAGGGT | 25929 |
| rs142261057 | snp | C/T | 4.9652e-05 | 0.00498232 | missense | GEMIN5 | GRCh38.p7 | 5:154892423 | ACACTTCCTGCATGA[C/T]GGTGAAGCTCCCTGA | 25929 |
| rs142282106 | snp | A/G | 0.000153988 | 0.00877328 | missense | GEMIN5 | GRCh38.p7 | 5:154891505 | GGCCTGTTTGGCTCT[A/G]GCTGAGAAGTTTCAG | 25929 |
| rs142314227 | snp | A/C | 0.000153988 | 0.00877328 | missense | GEMIN5 | GRCh38.p7 | 5:154889321 | TGCTTTAACTCTTAC[A/C]TTAATGCTCTCAGGA | 25929 |
| rs142323952 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154919447 | TAATTAAATGTGGGA[A/C]TCTGGGTAAAGGATA | 25929 |
| rs142324271 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154907194 | GCAAGTTCCCACAGT[C/G]GTGGTAGCTTCTAGG | 25929 |
| rs142530738 | snp | C/G | 0.00518391 | 0.0506467 | missense | GEMIN5 | GRCh38.p7 | 5:154917072 | AGATAGCTCAATTCT[C/G]GCTGGCTGCCATGCT | 25929 |
| rs142636823 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154909055 | ACTTGACCTTCCAGG[C/T]TCAAGCAATCCTCCT | 25929 |
| rs142716554 | snp | A/G | 0.00044469 | 0.0149046 | missense | GEMIN5 | GRCh38.p7 | 5:154907716 | TCATTTCCATCAATC[A/G]ATTCCAGCTTTACAG | 25929 |
| rs142735219 | snp | C/T | 1.66896e-05 | 0.00288869 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154927397 | TACATCTCTATCCAT[C/T]GATGTAGAAAGTAAT | 25929 |
| rs142749540 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154934106 | CTGCAACCTCCACTG[A/C]CCAGGTTCAAGCGAT | 25929 |
| rs142769106 | snp | A/C/G | 0.00069367 | 0.0186108 | missense | GEMIN5 | GRCh38.p7 | 5:154917042 | ATGACTGCATTGTTG[A/C/G]AGCCAGAGGCCATCA | 25929 |
| rs142787271 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154895004 | GAATTGCTTGAACCT[A/G]GGAGGCGGAGGTTGC | 25929 |
| rs142807733 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154901066 | CATGGTGGCTCATGC[C/T]TGTAATCCCAGCACT | 25929 |
| rs142812130 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154906285 | ACAGGCATGAACCAC[C/T]ATGCCCGCCTTACTT | 25929 |
| rs142987992 | snp | A/C | 0.0279526 | 0.114869 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154903279 | ACACCCACTTCAGAC[A/C]CTGAGAGAATCAGAG | 25929 |
| rs143020924 | snp | C/T | 0.000405609 | 0.0142352 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154936065 | TGTCAATGCTGAAGT[C/T]CTACTTAATTTTTAA | 25929 |
| rs143042894 | snp | A/G | 0.029116 | 0.117091 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154888919 | CTGGAGTGCAGTGGC[A/G]TGATCTTGGCTCACT | 25929 |
| rs143124806 | snp | A/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154920803 | AGACTTTTGATGAAT[A/T]CACTTATGTAAAAAG | 25929 |
| rs143168571 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154916403 | TATACATATGTAGGC[C/T]ATGACTTTATAAAAT | 25929 |
| rs143223643 | snp | A/C | 0.000153988 | 0.00877328 | missense | GEMIN5 | GRCh38.p7 | 5:154912963 | GGGCTCCACGCCACA[A/C]TGGTAATCTTGGCCG | 25929 |
| rs143259270 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154919698 | TTGTTGCAATTGAGA[C/T]AGACCTTTTTTTCAG | 25929 |
| rs143295209 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154917697 | ATTTTGTGAGGGACA[A/C]GACAGCCAAAATACA | 25929 |
| rs143316335 | snp | C/G | 1.65427e-05 | 0.00287595 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154898433 | GGAGATGAAATAACA[C/G]ACTGACCTGTAGACT | 25929 |
| rs143341664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154930708 | GGGGAAATGGAGAGT[A/G]GAATTCTGGAGATGG | 25929 |
| rs143392417 | snp | G/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154899983 | TTCAGTGTTGGGTAT[G/T]TGGCAGATGTTTTTC | 25929 |
| rs143405680 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154912908 | TAGTACCTGGGCTGT[A/G]CCATCATAGGAAGCA | 25929 |
| rs143445125 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154893900 | AGGAGCCCGCCACCA[C/T]GCGCGGCTAACACCG | 25929 |
| rs143505996 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154909800 | CCTAGCCAACATGGT[A/G]AATCCCTGTCTCTAC | 25929 |
| rs143582582 | snp | C/T | 0.000230597 | 0.0107352 | missense | GEMIN5 | GRCh38.p7 | 5:154888257 | AAGTTTTCGTGTTGC[C/T]GTATTTCTGAAGGAG | 25929 |
| rs143587993 | snp | A/G | 0.0113566 | 0.0744939 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154938047 | GGTCCGCGCGGCGAA[A/G]CCAAAGAGGCCCCCG | 25929 |
| rs143651727 | snp | C/T | 6.60578e-05 | 0.0057467 | missense | GEMIN5 | GRCh38.p7 | 5:154907809 | TTCTCCAATTCAATA[C/T]TTTTTTTGCCTACAA | 25929 |
| rs143675610 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154919066 | TAAGTAAATAAATAA[A/G]AATACTCATTTGAAA | 25929 |
| rs143679822 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154890913 | GAATTACAGGCATGT[A/G]CCACCATACCCAGCT | 25929 |
| rs143683822 | snp | G/T | 0.00107081 | 0.0231141 | missense | GEMIN5 | GRCh38.p7 | 5:154896231 | TCCACGAAAGGCCCT[G/T]CGGTGCCCGTGTTCC | 25929 |
| rs143721005 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | MRPL22, GEMIN5 | GRCh38.p7 | 5:154940108 | GAGGGGTCAAATACA[C/T]ATATTTGAAGGCGTC | 25929 |
| rs143778467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154923951 | ACAAAGATGAACTGT[A/G]TATGTAACCTAAAGT | 25929 |
| rs143906072 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154915861 | TACATCTTTTTACCT[A/G]GCAATTCCACTTCTA | 25929 |
| rs143925712 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154927020 | CACACCACTGCACTC[C/T]AGCCTGGGAGACAGA | 25929 |
| rs144150244 | snp | A/G | 0.0704125 | 0.17392 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154905959 | GCCTCCCAAACTGCT[A/G]GGATTACAGGCGTGA | 25929 |
| rs144152068 | snp | C/T | 0.000593217 | 0.0172121 | missense | GEMIN5 | GRCh38.p7 | 5:154917977 | CATCTGCTTTCCAAC[C/T]TATCTCTGTGTGTAC | 25929 |
| rs144244168 | snp | A/G | | | missense | GEMIN5 | GRCh38.p7 | 5:154905440 | GACTTTTCAAAGCCT[A/G]AGGAAACTGGAGTGC | 25929 |
| rs144244915 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154909407 | GTCTGGACTCATGAA[A/T]TCTTCCATTACTGTT | 25929 |
| rs144363013 | snp | C/T | 0.000477874 | 0.0154502 | missense | GEMIN5 | GRCh38.p7 | 5:154898553 | ACTCATCCTCTCCTA[C/T]GATGGCAGCCAACTC | 25929 |
| rs144376373 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154920532 | TCAAAGCAGTGATTT[C/T]CTTAGTATCACAGCA | 25929 |
| rs144462633 | snp | G/T | 8.25307e-05 | 0.00642328 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154907604 | ACCCGCTGGAGCAAG[G/T]CCACAGGGTAATTCC | 25929 |
| rs144546733 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154901162 | AAGACTCCGTCTCTA[C/T]AAAAAACTAAAAAAT | 25929 |
| rs144650408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154929517 | TTTAAAAAATACATA[C/T]GCCAGGGCCTAACTC | 25929 |
| rs144711443 | in-del | -/AAAC | 0.21875 | 0.248039 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154893097 | TGAGACTCCCTCTCA[-/AAAC]AAACAAACAAACAAA | 25929 |
| rs144738249 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154911375 | AAAAATTAGCCAGCA[C/T]GGTAGTGCGCACCTG | 25929 |
| rs144771715 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154910303 | GTTTAATATATTCTT[C/T]CATTTAAAATAAAAA | 25929 |
| rs144812582 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154914598 | AGCTAACTGTAGCCT[A/C]CAACTCCTGGGCTCA | 25929 |
| rs144819063 | in-del | -/T | 0.0228947 | 0.104514 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154916814 | CATTTTCTGTTACCA[-/T]TTTTTGTCATGTTTG | 25929 |
| rs144946657 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154913290 | CCTGCCTCAGCCTCC[C/T]AAGTCTAGGTGATTT | 25929 |
| rs144967413 | snp | C/T | 1.66344e-05 | 0.0028839 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154896284 | TTTGCCCTCTGAAAG[C/T]TGCTTTTCCTCCAGA | 25929 |
| rs145065910 | snp | C/G | 0.000153988 | 0.00877328 | missense | GEMIN5 | GRCh38.p7 | 5:154902626 | GATCTCCTTTCCAAA[C/G]CATAAGCTGGTGAAA | 25929 |
| rs145141214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154918600 | ATTAGAAGAGACTTA[A/G]GAACACGAATTTTGT | 25929 |
| rs145183985 | snp | C/T | 0.0448719 | 0.142907 | upstream-variant-2KB | MRPL22, GEMIN5 | GRCh38.p7 | 5:154939476 | CTTATCAGTTAATTG[C/T]ATCTTGGATGTGCTG | 25929 |
| rs145213403 | snp | C/G | 0.00062942 | 0.0177289 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154911869 | TCCTCGGAAATTGCA[C/G]AGGGGCTCTTCCCGG | 25929 |
| rs145227343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154930454 | TTATTTATAACAAGT[A/G]GATGAGTGGGTAAGT | 25929 |
| rs145253856 | snp | A/C | 3.29554e-05 | 0.00405914 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154932142 | ACAATCTTCACCAGG[A/C]AGGGGACACCAGGCT | 25929 |
| rs145276337 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154931316 | GTCTAGGCCAGGCTC[A/G]AATGAGGAAGCAGAA | 25929 |
| rs145307280 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154932919 | GAAAATAATCTCTTT[A/C]TTTATAAGTGATACT | 25929 |
| rs145389621 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | GEMIN5 | GRCh38.p7 | 5:154887147 | AAAATAAACTACAAA[C/T]GTGAGCAGAAAAGCC | 25929 |
| rs145403023 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154918059 | CTCACAAATCAGCAA[G/T]GACAGCATGAGAAAA | 25929 |
| rs145435069 | snp | A/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154907469 | CTTAACAAAAAAAAC[A/T]AATGCTGTTTCCAAG | 25929 |
| rs145580824 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154914822 | TTATATATTAAGTTA[A/T]ACTAACAAACTGATA | 25929 |
| rs145700526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154896413 | TCTCGAGAGCTCTCC[C/T]GTGTCCTTCAAAGTA | 25929 |
| rs145720289 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154904081 | ACTTACAAAGCAAAA[C/G]CTTCCATCAAATTTT | 25929 |
| rs145792837 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154888760 | ATCTATTTGGTTTCT[C/T]TGAAGATTGAGGTAT | 25929 |
| rs145830930 | snp | A/C/T | 0.00049639 | 0.0157478 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154892457 | ATAGCTCCGGACCAC[A/C/T]GCCCGAAGGAGCGCC | 25929 |
| rs145852757 | snp | A/G | 0.000164948 | 0.00908003 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154903114 | ATACAGGGTAGCCCT[A/G]TCTGTGAAAAGCCCC | 25929 |
| rs145868718 | snp | A/G | 1.6566e-05 | 0.00287797 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154924519 | ATCATCAGTTCCAAA[A/G]GCTAAGCAACCTTCC | 25929 |
| rs145899892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154935284 | TTTCAAATCCACTCC[A/G]ATCAGAATTTCTCCT | 25929 |
| rs145947546 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154888959 | GCCTCCTGAGTTCAC[A/G]CCATTCTCCTGCCTC | 25929 |
| rs146056500 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154906500 | ATGGTGTCACAATCC[C/T]GAGCACAGGAACTTT | 25929 |
| rs146075014 | snp | C/G | 1.6473e-05 | 0.00286988 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154891402 | TCTCTGTGAGTTTTG[C/G]AGACTGGCATGCTTT | 25929 |
| rs146092283 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154902192 | CACAATTAACAGAGC[C/G]CTATAGGTCTGAACG | 25929 |
| rs146114513 | in-del | -/A | 0.00676609 | 0.0577691 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154917454 | TTTCCACACTACCTC[-/A]AGTGTAACAATCTCC | 25929 |
| rs146180395 | snp | A/G | 0.000623006 | 0.0176384 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154926089 | CCTGCAAAGATTAAC[A/G]GTAAGGGCCTAAACA | 25929 |
| rs146215158 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154921071 | ATCAGGACCCAGCAT[C/G]ATAACTATACATACA | 25929 |
| rs146236849 | snp | C/G | 0.000153988 | 0.00877328 | missense | GEMIN5 | GRCh38.p7 | 5:154928578 | CTGGGCCAATGGAGT[C/G]TCAACCAAAGGCGCT | 25929 |
| rs146356009 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154923217 | CCCTGTCTGTCTCTA[C/T]TAAAGATACAAAATT | 25929 |
| rs146357980 | snp | G/T | 0.000153988 | 0.00877328 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154891606 | CCTTACCCAGACACT[G/T]GAATTTGGGCAAGGT | 25929 |
| rs146397981 | snp | A/C/T | 8.24512e-05 | 0.00642028 | missense | GEMIN5 | GRCh38.p7 | 5:154898475 | GCAGGGCTTCCTGGG[A/C/T]TCCCACCCAGTTGTT | 25929 |
| rs146429547 | in-del | -/TAAAAT | 0.0260105 | 0.111035 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154921007 | TCATTCTAATTCTGA[-/TAAAAT]TAAAAAGAGACAGCA | 25929 |
| rs146566831 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154919573 | AAACACCATGCAGTT[C/G]CATTTGGATACTATA | 25929 |
| rs146600005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154892990 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGACAGA | 25929 |
| rs146685959 | snp | A/C/T | 0.00469392 | 0.0482181 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154917892 | GATCAAATATATGTG[A/C/T]GATTGCAAATTTTTT | 25929 |
| rs146719950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154914720 | CAAGTGTTGGGATTA[C/T]AGGCATGAGCCACCA | 25929 |
| rs146806835 | snp | A/G | 0.00398564 | 0.0444627 | upstream-variant-2KB | MRPL22, GEMIN5 | GRCh38.p7 | 5:154940199 | TTGAGAGACTTTAAC[A/G]TATCCTAAATATGTT | 25929 |
| rs146816444 | snp | C/T | 0.000363564 | 0.0134778 | missense | GEMIN5 | GRCh38.p7 | 5:154911738 | TGACCTTGAGGAGGC[C/T]GGGAATGATCTTGCA | 25929 |
| rs146840662 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154934529 | GTTGGCCGGGCTGGT[C/T]TTGAACTCCTGACCT | 25929 |
| rs147083765 | snp | C/T | 3.29886e-05 | 0.00406118 | missense | GEMIN5 | GRCh38.p7 | 5:154925884 | ACCTTGGACTTCACG[C/T]CTTGCCAAAAATTTT | 25929 |
| rs147171245 | snp | C/T | 0.0010563 | 0.0229572 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154905391 | TGGTGGCTCCTTTTT[C/T]AGTAAAATGACTTTG | 25929 |
| rs147264136 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154915938 | GTATAAGGCAGTTTA[C/T]TGTAATACTACTTAA | 25929 |
| rs147296855 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154912530 | AGATTTCTGACTTAC[C/T]AATTTATTATTAAAA | 25929 |
| rs147370945 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154936706 | TGTTTTAGACCTTGT[A/G]GGCCATACCATGCCT | 25929 |
| rs147399993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154932489 | CTCTTGGCACTAGGT[A/G]ATACTATGTATGTTG | 25929 |
| rs147537034 | snp | C/T | 0.000190279 | 0.00975208 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154916958 | TGGAAAGTAGCTGAA[C/T]AAACGATATCATCCC | 25929 |
| rs147632748 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154933270 | ATATTCCTAAATAAG[A/G]TATAGATTTTGCATA | 25929 |
| rs147663997 | snp | G/T | 0.00517822 | 0.0506191 | downstream-variant-500B | GEMIN5 | GRCh38.p7 | 5:154887247 | ACTCTGATTTTCCCA[G/T]GCTAGCAACTGTGAC | 25929 |
| rs147736549 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154903475 | GGGATTCAATATTCA[C/T]CCTTTGCTTCAAAAA | 25929 |
| rs147746278 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154909019 | GAGTGCGGTGGCAGA[A/G]TCTCCGTTCACGGCA | 25929 |
| rs147765525 | snp | A/T | 0.0539725 | 0.156929 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154909723 | GTGGCTCATGCCTAT[A/T]ATCCCAGCACTTTGG | 25929 |
| rs147817295 | snp | A/G | 0.000592856 | 0.0172069 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154896170 | TTCCTGATACTGCTC[A/G]GGGGTGTCAAGGCTG | 25929 |
| rs147870255 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154929601 | CCAAAGACTCTCCAG[C/G]TGATTCTGCTGCACA | 25929 |
| rs147885463 | snp | A/T | 0.00178445 | 0.0298168 | missense | GEMIN5 | GRCh38.p7 | 5:154937992 | GGGGTGTCCCTGGAC[A/T]CTCGCCTGCGCCCGG | 25929 |
| rs147947604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154913566 | TGTCGGCTCACGCCT[A/G]TAATCCCAGCACTTT | 25929 |
| rs147970218 | snp | C/T | 1.64787e-05 | 0.00287038 | missense | GEMIN5 | GRCh38.p7 | 5:154927456 | GACATAAATTAAACA[C/T]AATTCTTGAATGATT | 25929 |
| rs147996733 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154909865 | GCACCTATAGTCACA[A/G]CTACTCAAAAGGCTG | 25929 |
| rs148050510 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154915256 | TCTTGTTACACATAG[C/G]ATTCTTAGAAAACTA | 25929 |
| rs148069198 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154901633 | GCCATTATGGATCAT[C/T]TGCTTCATCTACACA | 25929 |
| rs148092374 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154919197 | TTAGCTGGGCATGGT[G/T]GCCCATGCCTGCAGT | 25929 |
| rs148146488 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154924276 | TAGGGAACAGGGAAA[C/T]GAGTTAGAAGCTACC | 25929 |
| rs148166423 | snp | A/T | 0.000115471 | 0.0075975 | missense | GEMIN5 | GRCh38.p7 | 5:154903132 | TGTGAAAAGCCCCAG[A/T]TGAAATCTTTCCTCA | 25929 |
| rs148198781 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154889051 | CCGGCTAATATTTTG[A/T]ATTTTTAGTAGAGAC | 25929 |
| rs148229206 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154936234 | ATCCTGGCTAACATG[A/G]TGAAACCCCATCTCT | 25929 |
| rs148247015 | in-del | -/ATAC | 0.0352966 | 0.128072 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154914015 | CTAAAAAATAAATAA[-/ATAC]ACACATAATTTTTTT | 25929 |
| rs148342568 | snp | C/T | 0.000132608 | 0.00814166 | missense | GEMIN5 | GRCh38.p7 | 5:154912915 | TGGGCTGTACCATCA[C/T]AGGAAGCAGATACCA | 25929 |
| rs148426811 | snp | C/T | 0.000329625 | 0.0128337 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154898575 | AGCCAACTCTGCAGC[C/T]GTTCTAAGTGATGCC | 25929 |
| rs148477052 | snp | C/T | 0.000153988 | 0.00877328 | missense | GEMIN5 | GRCh38.p7 | 5:154907684 | CAGGTCCTGAGTTCT[C/T]CTTCATGCTTTCTTC | 25929 |
| rs148512362 | in-del | -/TTTTG | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154888856 | TCTAAATTCTTTTTT[-/TTTTG]TTTGTTTTGTTTTTT | 25929 |
| rs148521926 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154911460 | GGAGGCTGCAGCGAG[C/T]CAAGATCACGCCACT | 25929 |
| rs148584245 | snp | A/C/G | 0.0037151 | 0.0429395 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154916976 | ACGATATCATCCCCA[A/C/G]TATGAAAGAAACCAA | 25929 |
| rs148616356 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154920644 | ATCACAAATCAAATA[A/C]CCAGTAAACATTTGT | 25929 |
| rs148666577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154927818 | GCAACAAAGTGAGAC[C/T]GTCCCTACAAACAAT | 25929 |
| rs148705414 | snp | A/C/G/T | 0.000248335 | 0.0111406 | missense | GEMIN5 | GRCh38.p7 | 5:154935851 | CTTACCCAATGGCTA[A/C/G/T]TAAATCTTCATGATG | 25929 |
| rs148816132 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154909750 | TTGGGAGGCTGAGGC[A/G]GGCAGATCATCTGAG | 25929 |
| rs148897371 | in-del | -/A | 0.00914312 | 0.0669923 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154929744 | TAGCCTGTAAACCTT[-/A]AAAAAAGTTCTGTCT | 25929 |
| rs148983604 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154888648 | CCCTTAAAAATGGTG[C/T]TTCTATTAATATTTG | 25929 |
| rs149015090 | snp | A/G | 0.000346623 | 0.0131602 | missense | GEMIN5 | GRCh38.p7 | 5:154903157 | TCCTCAACATCAGCA[A/G]ACACATCTTCATTCA | 25929 |
| rs149056180 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154914307 | ATTATAGGCGTGAGC[C/T]ACCACGCCCGGCCTA | 25929 |
| rs149109713 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154919020 | CACTCCAGCCTGGGC[A/G]ACAGAACAAGGCTCT | 25929 |
| rs149158951 | snp | A/C | 8.23662e-05 | 0.00641688 | missense | GEMIN5 | GRCh38.p7 | 5:154902621 | TTTGAGATCTCCTTT[A/C]CAAAGCATAAGCTGG | 25929 |
| rs149193139 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154930586 | AAGTGAAATAAGCCA[A/G]TCACAAAAAGACATA | 25929 |
| rs149213311 | snp | C/G | 1.65828e-05 | 0.00287943 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154911872 | TCGGAAATTGCACAG[C/G]GGCTCTTCCCGGAGA | 25929 |
| rs149245342 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154893813 | CAGTGGCACGATCTC[A/G]GCTCACTGTAAGCTT | 25929 |
| rs149342015 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154911241 | GATCTGGGCTGGGCA[C/T]GGTGGCTCATGCCTG | 25929 |
| rs149469432 | snp | C/G/T | 0.00182123 | 0.0301228 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154935791 | AAAGAAAATGCAAAA[C/G/T]ACGATCATAAACAAA | 25929 |
| rs149500994 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154905609 | ACCAAAACTTTTGAG[A/G]TAAAATGCACTGGAA | 25929 |
| rs149562947 | snp | A/C | 1.64732e-05 | 0.0028699 | missense | GEMIN5 | GRCh38.p7 | 5:154891351 | TTGGTGTTGTCGGAT[A/C]ATTTCTGCCAAGGTC | 25929 |
| rs149615722 | snp | C/T | 1.64798e-05 | 0.00287047 | missense | GEMIN5 | GRCh38.p7 | 5:154898513 | AGCAGCTCTTGGGCA[C/T]ATCTGAGAGCCAGGG | 25929 |
| rs149760614 | in-del | -/A | 0.0955749 | 0.196603 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154916271 | ATTGTAAATTTAGAG[-/A]AAAAAAACTGCAAGC | 25929 |
| rs149782542 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154896019 | TCTGCTTGTTTCCCC[A/G]TTACAATAGACATGG | 25929 |
| rs149836438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154902810 | GATGGGTGTCACCTA[C/T]CAGAGTGATTACAGT | 25929 |
| rs149877560 | snp | C/T | 0.000423057 | 0.0145379 | missense | GEMIN5 | GRCh38.p7 | 5:154891737 | TGTCTCTTAGGTGGT[C/T]ACAGCCTAGGAAAAG | 25929 |
| rs149899431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154926775 | ACTAGGCCAGGCGCC[A/G]TGGCTCACGCCTGTA | 25929 |
| rs149927915 | snp | C/T | 3.29468e-05 | 0.00405861 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154902567 | AGCCACAAGGTTGTC[C/T]GTCAGCTCCCCTCTT | 25929 |
| rs149994085 | snp | G/T | 0.0260105 | 0.111035 | upstream-variant-2KB | MRPL22, GEMIN5 | GRCh38.p7 | 5:154939451 | TTGCGGATATTGCTC[G/T]CCACAGTATCTTATC | 25929 |
| rs150001407 | snp | C/T | 0.000153988 | 0.00877328 | missense | GEMIN5 | GRCh38.p7 | 5:154931556 | TGTGCTACAGCATTC[C/T]CGTTGGTAATTTCAG | 25929 |
| rs150254240 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154934430 | GATTTGCCCACCTCG[C/G]CCTCTCAAAGTGCTG | 25929 |
| rs150306628 | snp | A/C | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154899572 | GGGTTCATGAGGTTA[A/C]AACTATTTTCGTAAC | 25929 |
| rs150356965 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154904723 | AACCTACTGGCAGGA[C/T]GACACCACAGGCAGA | 25929 |
| rs150401997 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154915735 | AGATGCAATCAAACA[A/C/T]GGGAATGAGGTATGT | 25929 |
| rs150433886 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154930232 | TTAGTTTAGCCTGTG[C/T]GGTCTAACCCTAGCT | 25929 |
| rs150536772 | snp | C/T | 0.000115572 | 0.00760082 | missense | GEMIN5 | GRCh38.p7 | 5:154932105 | CATCTCTACCTGAAG[C/T]TTCCTCTTGGTTTAT | 25929 |
| rs150581460 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154901744 | CACAGTTAAATTCCT[A/G]TAATCATAACTGATG | 25929 |
| rs150663121 | snp | G/T | 0.000247062 | 0.0111117 | missense | GEMIN5 | GRCh38.p7 | 5:154904563 | TGAAGCTCCTCTTTG[G/T]ATCTGTGGTCCAGGC | 25929 |
| rs150747178 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154890054 | TGCTGTACTGTTTTC[C/T]ACAGTGGCTGCATCA | 25929 |
| rs150800940 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154895570 | ACTTTGCCCTACTGT[G/T]TTTATTTTATAAAGT | 25929 |
| rs150844531 | snp | A/G | 4.97739e-05 | 0.00498844 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154907835 | TACAAGAATCACAAT[A/G]AAGGACTGACTAAAG | 25929 |
| rs150926825 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154917529 | AATGACAAATGATGA[C/T]AGGGAGAAGCTAAAA | 25929 |
| rs150976510 | snp | C/G | 0.000889665 | 0.0210723 | missense | GEMIN5 | GRCh38.p7 | 5:154907776 | TTGGGCTTTGCCTTA[C/G]GTTGAGAGAGCCGTT | 25929 |
| rs150980009 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154921824 | CATTTCCTAAATTGA[C/G]ACAAGATTTCAGGGT | 25929 |
| rs151076397 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154934164 | GGGCTTACAGGTGTG[A/C]GCCACCAAGTCTGGC | 25929 |
| rs151234175 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154928052 | GGGAAGACAGAAAGA[C/T]AGTTTATTATATACT | 25929 |
| rs151275364 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154892240 | TGTTCTTAAAAGCTT[C/T]GGTAAGAGAATCCAA | 25929 |
| rs151292988 | snp | C/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154930476 | TGGGTAAGTAAAATG[C/T]GGGACATACACACAA | 25929 |
| rs151337581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154898777 | GTCCCAGGTATGTCA[C/T]TGCCCCGGTTGTTCC | 25929 |
| rs180840178 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154918150 | ACATAATTAGTAAAA[A/G]GATTACTAAGAACAT | 25929 |
| rs180841911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154934804 | TGGGCCTATAATTTT[C/T]CTTAGTACATTCGTT | 25929 |
| rs180961296 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154922058 | TTAGCAGCTGACTTA[C/T]TTCCATTTATCTGAC | 25929 |
| rs180966168 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154894600 | ACATGGTGAAACCCT[A/C/G]TCTCTACTAAAAATC | 25929 |
| rs180968573 | snp | C/G | 0.00279162 | 0.0372561 | upstream-variant-2KB | MRPL22, GEMIN5 | GRCh38.p7 | 5:154940062 | GCATAGGTAGCAAAC[C/G]GCAATCTGAACTACC | 25929 |
| rs180984584 | snp | C/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154913226 | GGCGCAATGCAATGG[C/T]GCAATCTCGGCTCAC | 25929 |
| rs181023103 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154930283 | GCAGGGGCCACATGC[A/G]TCAGGGATAAGAACC | 25929 |
| rs181064952 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154911989 | AAACAAAAAACAAAA[A/C]ACAAAAACAATCTGC | 25929 |
| rs181065453 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154902980 | GACACGTAAAACTAA[C/G]CATTATAATATCACA | 25929 |
| rs181069305 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154893388 | TAAGCCACTACACCC[A/G]AGCCTGGGTGACAGA | 25929 |
| rs181075546 | snp | A/G | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154929233 | TGCCTCAAAAGAAAA[A/G]GAGTATTTTTTCGTC | 25929 |
| rs181157045 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154903637 | GACACAAGAAACTGA[C/T]AATAGTTTGATTATG | 25929 |
| rs181175183 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154922375 | GGTTTCACAGTGTTA[G/T]CCAGGATGGTCTCGA | 25929 |
| rs181296339 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | GEMIN5 | GRCh38.p7 | 5:154888149 | CTGGTGAGGCATAAC[C/T]GCAGAGGTGAAAGAT | 25929 |
| rs181304133 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154927150 | ACATCCTTCCCTGGG[A/C]AAAACTACCCTTCTT | 25929 |
| rs181313853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154899378 | GGTCCTAGGAGGGGC[C/T]GTAAGACAGGACAAA | 25929 |
| rs181401506 | snp | C/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154907994 | ACCCTTTTGAAATTT[C/T]ATTAAATCATAAACA | 25929 |
| rs181617405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154908477 | TGAGCCACCACGCCC[A/G]GCCTACCCAGATGTC | 25929 |
| rs181633853 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154927648 | GCTGCAAAATGATTT[C/G]TTGTCGTTTAAGGAG | 25929 |
| rs181712966 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154889066 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 25929 |
| rs181729957 | snp | A/G | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154937664 | CCAGGAAGGCTCCCG[A/G]GGGGCTGGCGCGCAC | 25929 |
| rs181799692 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154928007 | AAAAAAAAAAAAAAT[G/T]TAATCACAGAAAGGG | 25929 |
| rs181823901 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154898076 | CGGCTAATTTTTGTA[G/T]TTTTAGTTGAAACGG | 25929 |
| rs181978373 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154934226 | AGTTTCGCTCTTGTT[G/T]CCCAGGCTGGGGTGC | 25929 |
| rs181981720 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154909070 | CTCAAGCAATCCTCC[G/T]GCCTCAGCCTCTTGA | 25929 |
| rs182159132 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154894192 | TCAAGCGATCCACCC[A/G]CGTTGGCCTCCCAAA | 25929 |
| rs182168379 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154897510 | TCTCTTTTTTTTCTG[A/C]AGAGTCTCACTCTGT | 25929 |
| rs182168952 | snp | A/G | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154929868 | TGATAAAACTATCAT[A/G]GTTTCAAATAAAGTA | 25929 |
| rs182184802 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154901669 | AAGCATCAATTGTTT[C/G]ATTATGTAACACAAA | 25929 |
| rs182200729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154937520 | ACCTGGCATGTCATA[C/T]CCTAAGGCACAATCA | 25929 |
| rs182202270 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154920474 | TCTTTGGGAATTACA[C/T]AGCACAGTAGGACTT | 25929 |
| rs182255826 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154916680 | TTTTCAATTTTTTGT[A/T]GAGACGGAGCCTCAC | 25929 |
| rs182269175 | snp | C/G/T | 3.3278e-05 | 0.00407898 | missense | GEMIN5 | GRCh38.p7 | 5:154889401 | GCAGAGAAAGTGGCT[C/G/T]ATTTTTTTCTTCTTT | 25929 |
| rs182311609 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154923621 | GAAATCTGAATTTTA[C/T]TTAATCTTCATATGT | 25929 |
| rs182435845 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154912533 | TTTCTGACTTACCAA[C/T]TTATTATTAAAAAAT | 25929 |
| rs182527685 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154891035 | TGCTGGGATTACAAG[C/T]GTGATCCACTGTGCC | 25929 |
| rs182554697 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154928081 | CTTTCGTTCTTCTTG[A/G]ACCATGTGAGTATAT | 25929 |
| rs182577490 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154913389 | CAAGAAGTGTTAGGT[C/G]TCATTATAACTTATA | 25929 |
| rs182579083 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154894984 | CTTGGAAGGCTGAGG[C/G]AGGAGAATTGCTTGA | 25929 |
| rs182821841 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154909876 | CACAGCTACTCAAAA[C/G]GCTGAGGCAGGAGAA | 25929 |
| rs182854661 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154905091 | CCCAGCTACTCGGGA[A/G]GCTGAGGCAGGAGGA | 25929 |
| rs182861926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154922943 | CCTCAGGATCCGCCC[A/G]CCTCAGCCTCCCAAA | 25929 |
| rs182912223 | snp | A/T | 0.000136902 | 0.00827238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154932284 | AAATATTACTAAAAA[A/T]ATGAAGACAGAACAG | 25929 |
| rs183065048 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154919578 | CCATGCAGTTGCATT[G/T]GGATACTATATTATT | 25929 |
| rs183066599 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154901101 | GAGGCTGAGGCACGA[A/G]GATCGCTTGAGCCCA | 25929 |
| rs183079456 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154928912 | GGCTATCTTGACAAC[C/G]TCAACGTATTAAGAG | 25929 |
| rs183083508 | snp | A/G | 0.000201694 | 0.0100402 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154924596 | GAATATAAGAAGTGG[A/G]GCATATAGTTAAAGG | 25929 |
| rs183157662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154910295 | TTCTAGTTGTTTAAT[A/G]TATTCTTTCATTTAA | 25929 |
| rs183163334 | snp | C/T | 1.64768e-05 | 0.00287021 | missense | GEMIN5 | GRCh38.p7 | 5:154891538 | TCCGTTTCTTCAGTG[C/T]TGGCAGTGTCTAACT | 25929 |
| rs183399540 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154895358 | AAAAAAAAAAAGAAG[C/T]AGGTATATTCACAAG | 25929 |
| rs183416103 | snp | C/T | 1.65282e-05 | 0.00287469 | intron-variant, splice-acceptor-variant | GEMIN5 | GRCh38.p7 | 5:154931579 | AATTTCAGCTTCTTC[C/T]ATGAGATAGGTGGCA | 25929 |
| rs183576538 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154919110 | AAAGCAGGTGGATCA[C/T]TTGAGCTCAGAAGTT | 25929 |
| rs183616208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154893054 | GTGAGCTGAGATTGC[A/G]CCACTGCACTCCAGT | 25929 |
| rs183656851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154914090 | CAATGGCACGATCTC[A/G]GCTCAATGCAACCTC | 25929 |
| rs183660330 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154936819 | CCTATTTGCAAAAAC[A/C]GGCACAGAGCAGTTT | 25929 |
| rs183661559 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154914312 | AGGCGTGAGCCACCA[C/T]GCCCGGCCTAAATAA | 25929 |
| rs183783604 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154900400 | GCCATGATGGAGTAA[A/C]TGGGACCAGACTTAC | 25929 |
| rs183804822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154935357 | AATAGACATCTTTCA[A/G]TGAGAAGTACATGAA | 25929 |
| rs183834096 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154897422 | CAAAAAGGCAGTGGT[A/C]TGTTACTGATTTTTA | 25929 |
| rs183841932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154915541 | ATTAAGCATGGAATA[A/G]TACTTGCTAGAACAC | 25929 |
| rs183842342 | snp | A/G | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154933240 | TGTTATATCATTCCT[A/G]GCCTTTCTTTGTATA | 25929 |
| rs184233612 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154929176 | TTGCAGTGAGCTGAG[A/T]TCGTGCCACTGCACT | 25929 |
| rs184374974 | snp | A/G | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154911242 | ATCTGGGCTGGGCAC[A/G]GTGGCTCATGCCTGT | 25929 |
| rs184404340 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154912410 | CAACTCAACACTAAG[C/T]GAGATACATCACAGA | 25929 |
| rs184407477 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154893600 | CGGCTCCTCTGCAGG[C/T]GATCTCCTGGCCCCA | 25929 |
| rs184416875 | snp | A/G | 0.00398564 | 0.0444627 | utr-variant-3-prime | GEMIN5 | GRCh38.p7 | 5:154887481 | TCCAAGAAAGTTTAA[A/G]AACCATTGAAACAGT | 25929 |
| rs184420950 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154929565 | GTAGATCTGAGGTGG[C/G]GTACAAGAACCTACA | 25929 |
| rs184434861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154925746 | TAGTTTCAAACTTCA[C/T]TGAAAATACTTTAAA | 25929 |
| rs184523133 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154906786 | TAACAGCTATCCCTT[C/G]GGATGGAGAGCATCA | 25929 |
| rs184542185 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154907207 | GTGGTGGTAGCTTCT[A/C]GGTCAGACATTTGTA | 25929 |
| rs184762925 | snp | C/T | 0.000691916 | 0.0185871 | missense | GEMIN5 | GRCh38.p7 | 5:154902542 | CAAAAACCATACCTG[C/T]TGGTGCCATAGCCAC | 25929 |
| rs184936710 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154908038 | CACCCAAATATTTTA[C/G]TGTGTGTCTTATGAA | 25929 |
| rs185039459 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154927237 | TGTGAGCTATTGATA[C/T]ATTCAGTGCTGATCT | 25929 |
| rs185069042 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154921536 | CATAACTACTAATAA[G/T]TGGAGAAAAATAATT | 25929 |
| rs185072535 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154897683 | GTAGAGACAAGATTT[C/T]GCCATGTTGGCCAGG | 25929 |
| rs185073120 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | GEMIN5 | GRCh38.p7 | 5:154938775 | GTGGTGGCAGGCGCC[G/T]GTAATCCCAGCTGCT | 25929 |
| rs185099367 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154934118 | CTGCCCAGGTTCAAG[C/T]GATTCTCCTGCCTCA | 25929 |
| rs185209138 | snp | A/G | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154915724 | TTGTGAGAATCAGAT[A/G]CAATCAAACACGGGA | 25929 |
| rs185232742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154921129 | ACAATGCTTTAGTGA[A/G]TTTGGGGAAGCTTAT | 25929 |
| rs185241738 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154922257 | ACTGCAAGCTCCGCC[C/T]CCTGGGTTCACACCA | 25929 |
| rs185245581 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154894869 | CCAAGATCATGCCAC[C/T]GTACTCCAGCCCGGG | 25929 |
| rs185253647 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154913268 | CCTCCTGGGTTCAAG[C/T]GATTCTCCTGCCTCA | 25929 |
| rs185308205 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154888682 | CCACAGCCAAAAAGA[C/G]CTGTCCATCTGTAAG | 25929 |
| rs185323458 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154934485 | CCTGGCCTGATTTTT[A/T]ATTTTTAGTAGAGAT | 25929 |
| rs185338939 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154902379 | GCTTTTTTTCAAAGG[A/G]GTTGGGTTGGATTTA | 25929 |
| rs185361790 | snp | C/G | 0.00318978 | 0.0398085 | upstream-variant-2KB | GEMIN5 | GRCh38.p7 | 5:154938649 | GCACTTTGGGAGGCC[C/G]AGGCGGGAGGATCAC | 25929 |
| rs185396758 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154911068 | AGCTGTTTCTTTTGT[C/T]CTTTTGACATGTCTC | 25929 |
| rs185512036 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154892902 | AGGAGTTCAAGACCA[G/T]CCTGGCCAACATGGT | 25929 |
| rs185523074 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154929084 | AAAAAATTAGCCGGG[C/T]GTGGTGGCAGGCACC | 25929 |
| rs185784579 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154889106 | TGGTCTTGATCTCCT[A/G]ACCTCATGATCCGCC | 25929 |
| rs185797576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154908490 | CCGGCCTACCCAGAT[A/G]TCTTTTATAGCAAAA | 25929 |
| rs185806114 | snp | C/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154931100 | TTTATTCTGCATTTG[C/T]GCATTAAAAGCTCTA | 25929 |
| rs185806858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154927654 | AAATGATTTGTTGTC[A/G]TTTAAGGAGAGAAAA | 25929 |
| rs185868417 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154903538 | AATAATGTGAAACTA[A/G]GTTAACTATGTAAGT | 25929 |
| rs185877584 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154935072 | CTGCATTTATCATAG[A/T]TTACTCCTGCAACAA | 25929 |
| rs185881333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154918606 | AGAGACTTAGGAACA[C/T]GAATTTTGTCTCTTA | 25929 |
| rs185966482 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154889894 | ACTTAGGTTGCTCCC[A/G]TGTTTTGGGTATTAT | 25929 |
| rs185976556 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154928042 | CAAGTAGCTAGGGAA[C/G]ACAGAAAGACAGTTT | 25929 |
| rs186103696 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154909701 | AATTTCACATACACC[A/G]GGCGCAGTGGCTCAT | 25929 |
| rs186447861 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154923378 | AGAGCGAAACTCTGT[C/G]TCCAAAAAAAAAAGG | 25929 |
| rs186554691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154914727 | TGGGATTATAGGCAT[A/G]AGCCACCACACGTAG | 25929 |
| rs186559168 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154896815 | AGCCATGTCCAAATA[A/G]GTTTAATAGAGGAAG | 25929 |
| rs186569993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154932746 | TTTTGTATTTTTTTG[C/T]AGAGATGAGGTTTCA | 25929 |
| rs186602810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154936143 | TTAATACGGCCGGGC[A/G]CGGTGGCTCACGCCT | 25929 |
| rs186683708 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154920179 | GCTATAGTATGACCA[C/T]ACCATACTACATAGT | 25929 |
| rs186687071 | snp | G/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154901109 | GGCACGAGGATCGCT[G/T]GAGCCCAGGAGTTGG | 25929 |
| rs186690633 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154900807 | ACAATTCCCAGAGCT[C/T]ACTCAGGACTTGGAG | 25929 |
| rs186696021 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154936820 | CTATTTGCAAAAACA[C/G]GCACAGAGCAGTTTG | 25929 |
| rs186728748 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154900252 | CAACTCAGTAAACAA[A/C]TATTTTTCAAATGAC | 25929 |
| rs186764575 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154922510 | TGGCAAAATGCCTAA[A/C]AATAGCTCTAGGGCA | 25929 |
| rs186828460 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154919194 | AAATTAGCTGGGCAT[A/G]GTGGCCCATGCCTGC | 25929 |
| rs186976040 | snp | A/T | 0.0209421 | 0.100162 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154903834 | AAAAATTAAAAAAAA[A/T]TTTTTTTTTTTAAAT | 25929 |
| rs187141885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154937608 | ATGCCACACGTTGCA[A/G]GATCTTGCTTAGGGC | 25929 |
| rs187333700 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154891051 | GTGATCCACTGTGCC[C/T]GGGCTTTTTTTTTTT | 25929 |
| rs187346346 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154910078 | TTTTTCTAGATTCAT[A/C/T]CATTTTGTTCTTTAT | 25929 |
| rs187393331 | snp | C/G/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154912553 | TATTAAAAAATTGTT[C/G/T]TGTGATTTTTAGCCA | 25929 |
| rs187403846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154910502 | TAGAAATGGGATCTC[A/G]CTCTGTTGCCAGGCT | 25929 |
| rs187406726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154891875 | AACAGTGTGATCCAC[C/T]GGGCCACATGCCTTT | 25929 |
| rs187420311 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154928950 | TTTTTTTGGCCGGGC[A/G]CGGTGGCTCATGCCT | 25929 |
| rs187534450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154895171 | TGAGAAGCCTTGTTC[C/T]TCATAAATATCATAA | 25929 |
| rs187539224 | snp | C/G | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154913627 | TCAGGAGTTCAAGAC[C/G]GGCCTGTGGAAACCC | 25929 |
| rs187542130 | snp | C/T | 6.60208e-05 | 0.00574509 | missense | GEMIN5 | GRCh38.p7 | 5:154931460 | AGATCAATCTTACCT[C/T]GGCCTCTAGAACAGC | 25929 |
| rs187628289 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154892927 | CATGGTGAAACCCCG[C/T]CTCTACTAAAAACAC | 25929 |
| rs187631450 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154894210 | TTGGCCTCCCAAAGT[A/G]CTGGGATTACAGGTG | 25929 |
| rs187651026 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154929998 | TTCAAAGAATCAATA[C/T]GTCAGTATGTTCAAT | 25929 |
| rs187748536 | snp | C/T | 0.000367297 | 0.0135467 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154924425 | GGGTGGCCAACCTTT[C/T]GGCTCCCCGGGCCAC | 25929 |
| rs188102885 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154920874 | AAGACAAGGCTGAGG[G/T]GCTAGAAGAGGGAAA | 25929 |
| rs188107428 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154917827 | AATCAAAATACCAAA[C/T]ACAACTGGGCCGCCC | 25929 |
| rs188113010 | snp | C/T | 0.00238145 | 0.0344246 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154899362 | AGGCTCCTCTGTGTA[C/T]GGTCCTAGGAGGGGC | 25929 |
| rs188123418 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154934558 | CTCAGGTGATCCACC[C/T]GCCTCGGCCTCCCAA | 25929 |
| rs188363991 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154901894 | AGCCTTAACCTCCCC[A/G]GGCTCAGGTGATCCT | 25929 |
| rs188365940 | snp | A/C | 0.0023381 | 0.0341113 | missense | GEMIN5 | GRCh38.p7 | 5:154928652 | GGGCAATTTCAAAAT[A/C]ATCACCCCTGCAGAT | 25929 |
| rs188420129 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154924712 | AAAACAAAGTCGGCC[A/G]GGCGCAGTGGCTCAC | 25929 |
| rs188508749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154888731 | CAATTTAAATTTTAC[C/T]TCTTACCTATTAAAT | 25929 |
| rs188514880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154933265 | TGTATATATTCCTAA[A/G]TAAGATATAGATTTT | 25929 |
| rs188518541 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154915636 | ACTTGCTTGAATAAG[C/T]TAGCTAACCTTTCTG | 25929 |
| rs188533234 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154908369 | TATTTTCAGTAGAGA[C/T]GGGGTTTCACCATGT | 25929 |
| rs188539112 | snp | C/T | 0.000273061 | 0.0116814 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154927582 | TAAGCATTAGTTCTT[C/T]TACAAACGATCTGAA | 25929 |
| rs188658912 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154893343 | GCTGAGGCGGAAGAA[C/T]TGCTTGAACCCGAGA | 25929 |
| rs188669035 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154911278 | TAGCACTTTGGGAGG[C/T]TGATAGGCAGATCAC | 25929 |
| rs188683954 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154929187 | TGAGATCGTGCCACT[A/G]CACTCCAGCCTGGGC | 25929 |
| rs188706433 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154906425 | ATAAAGTACTAATTG[C/T]ATATTTAATTACACT | 25929 |
| rs188732558 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154929085 | AAAAATTAGCCGGGC[A/G]TGGTGGCAGGCACCT | 25929 |
| rs188765392 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154929667 | AGTCTAGAGGTTACC[C/G]TCCTGGAGGGATCCT | 25929 |
| rs188885853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154914289 | GCCTCCCAAAGTGCC[A/G]GGATTATAGGCGTGA | 25929 |
| rs188981306 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154907259 | CAAATGTGGCTACTG[A/T]TGTCATACTGTTAAA | 25929 |
| rs189013386 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154911117 | GCCTTCCTTTCTGGC[A/G]TAAGAATGTTCCAGG | 25929 |
| rs189174453 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154931873 | ACAAAATTAGCTGGG[C/T]GTGGTGGCGCATGCC | 25929 |
| rs189246444 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154895505 | AGGAGGTGCCTGTGG[C/T]GAGCTAGGGAAGGAG | 25929 |
| rs189267042 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154926910 | AAAAATTAGCTGGGC[A/G]TAGGTGATACACGCC | 25929 |
| rs189354930 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | GEMIN5 | GRCh38.p7 | 5:154887487 | AAAGTTTAAGAACCA[C/T]TGAAACAGTAATTTA | 25929 |
| rs189440893 | snp | A/G/T | 0.00115471 | 0.0240007 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154902692 | CTGTTTGAAAGAGAG[A/G/T]TAATGTTTGGAAGGT | 25929 |
| rs189450360 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154922021 | CTTTGTATGATTGTA[C/G]AATTCCAGAGCCTAT | 25929 |
| rs189450589 | snp | C/G | 0.0263992 | 0.111815 | upstream-variant-2KB | GEMIN5 | GRCh38.p7 | 5:154938792 | TAATCCCAGCTGCTC[C/G]GGAGGCTGAGGCAGG | 25929 |
| rs189531592 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154897484 | AAGAGATTTCCATTT[A/T]CCCACACTTTTCTCT | 25929 |
| rs189578989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154906829 | ATCCTATATTCTAGC[C/T]ATTTCAATACTGTCA | 25929 |
| rs189643507 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154922314 | CTGGGACTACAGGCA[A/C]CTGCCACCAAGCCCG | 25929 |
| rs189793326 | snp | C/T | | | upstream-variant-2KB | GEMIN5 | GRCh38.p7 | 5:154938685 | CAGGAGTTAAAAGAC[C/T]GGCCTGGTCAGCATA | 25929 |
| rs189884393 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154902380 | CTTTTTTTCAAAGGG[G/T]TTGGGTTGGATTTAT | 25929 |
| rs189985699 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154903540 | TAATGTGAAACTAGG[G/T]TAACTATGTAAGTTA | 25929 |
| rs190055630 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154893892 | GGGACTACAGGAGCC[C/T]GCCACCACGCGCGGC | 25929 |
| rs190134132 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154921195 | ATCATCTGCCACTAC[G/T]GTCTTCATGAACCCC | 25929 |
| rs190149568 | snp | C/T | 3.29516e-05 | 0.00405891 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154891525 | AGAAGTTTCAGGGTC[C/T]GTTTCTTCAGTGCTG | 25929 |
| rs190159975 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154910290 | TAAATTTCTAGTTGT[G/T]TAATATATTCTTTCA | 25929 |
| rs190173822 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154928791 | AGAATTCAGATCTCA[C/T]TTTCCAATGGTTACA | 25929 |
| rs190309579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154913379 | TAGATTACCACAAGA[A/G]GTGTTAGGTCTCATT | 25929 |
| rs190315551 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154894881 | CACTGTACTCCAGCC[C/T]GGGTGACAGAGTGAG | 25929 |
| rs190320257 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154931189 | TTTTTATTACAAATA[C/T]TCTGCTCTCCATGCC | 25929 |
| rs190525240 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154916431 | AATCTAGAGAAAATA[C/T]ATAGCAAGCCAATAA | 25929 |
| rs190629280 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154909735 | TATAATCCCAGCACT[C/T]TGGGAGGCTGAGGCG | 25929 |
| rs190763651 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154897903 | GGGCTGACTAAGGTG[G/T]TTTTTTTTGTGTTTT | 25929 |
| rs190793327 | snp | A/G | 0.000148477 | 0.00861489 | stop-gained | GEMIN5 | GRCh38.p7 | 5:154931461 | GATCAATCTTACCTC[A/G]GCCTCTAGAACAGCT | 25929 |
| rs190795088 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154905296 | GTTTTTTGACAGTTG[C/T]GTGTAATATATGTAA | 25929 |
| rs190808911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154923590 | ATGTCCCAATAAAAT[C/T]TCACTTACAGACACT | 25929 |
| rs190872219 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154890911 | TGGAATTACAGGCAT[A/G]TGCCACCATACCCAG | 25929 |
| rs190944395 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154908980 | TCTTTTTTGAGACAG[G/T]TTCTTGCTCTGTTGT | 25929 |
| rs190950517 | snp | C/T | 0.00727789 | 0.059883 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154889301 | TGATGCTTTACCAAA[C/T]GAACTGCTTTAACTC | 25929 |
| rs190965727 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154927734 | CAGTAGTTCACATCT[A/G]TAATCTCAGCATTCT | 25929 |
| rs190972976 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154901099 | GGGAGGCTGAGGCAC[G/T]AGGATCGCTTGAGCC | 25929 |
| rs191097682 | snp | C/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154935320 | ATTCTAGGGAAATTG[C/T]TTAAGTCTTCAAATT | 25929 |
| rs191170153 | snp | C/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154900269 | ATTTTTCAAATGACA[C/T]ACAACTGCTGAGTTG | 25929 |
| rs191334487 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154918671 | AAGACAATGAGGGAA[C/T]ATAATCAACAATATA | 25929 |
| rs191440006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154901200 | ATGTGGTGGCATGCA[C/T]CTCCTGAGTAGTCCC | 25929 |
| rs191450190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154920186 | TATGACCATACCATA[C/T]TACATAGTTGTTTTA | 25929 |
| rs191450483 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154937365 | TTGGCTGTGCCACGT[A/G]ACTTCGAACAAGTCT | 25929 |
| rs191662026 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154922942 | ACCTCAGGATCCGCC[C/T]GCCTCAGCCTCCCAA | 25929 |
| rs191679338 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154895188 | CATAAATATCATAAT[C/G]TTCCCTCATTTTGAA | 25929 |
| rs191685081 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154914738 | GCATGAGCCACCACA[C/T]GTAGCCTAAACTATT | 25929 |
| rs191689815 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154897418 | GTGTCAAAAAGGCAG[C/T]GGTATGTTACTGATT | 25929 |
| rs191703731 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154932825 | CTGCGTTGGCCTCCT[A/G]AAGTGATGGGATTAT | 25929 |
| rs191745599 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154913674 | ATACAAAAATTAACC[A/G]GGTGTGTTGGTGCAC | 25929 |
| rs191885718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154930120 | CACCCTGACTCATTC[C/T]GATTTCCTGCTCTGC | 25929 |
| rs191945482 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154894523 | CACTTGTAATCACAG[A/C]ACTTTGGGAGGCCGA | 25929 |
| rs192026462 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154919564 | TCTTGAGTAAAACAC[C/G]ATGCAGTTGCATTTG | 25929 |
| rs192292082 | snp | A/C | 0.0013312 | 0.0257648 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154913082 | TGCTACTACTAATAA[A/C]AAAAAACAAAACAAA | 25929 |
| rs192326302 | snp | A/G | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154906644 | TCAAGCGGTTCTCCT[A/G]CCTCAGCCTCCTGAG | 25929 |
| rs192331743 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154924732 | CAGTGGCTCACGCCT[A/G]TAATCCCAGCACTTT | 25929 |
| rs192385576 | snp | C/G | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154936310 | TAGTTCCAGCTACTC[C/G]AGAGGCTGAGGCAGG | 25929 |
| rs192395528 | snp | A/G | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154925145 | AATGAGTTCAAATAC[A/G]TAAATGATATGCATT | 25929 |
| rs192473634 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154906995 | TAAATGTACAAAATA[A/C]AAAGAGTGCTAAAAT | 25929 |
| rs192508231 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154911144 | CAGGTTCAGTTTGTT[C/T]TCTACCTGTCCCAGA | 25929 |
| rs192527121 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154929006 | AGGCGGGAGGATCAC[A/G]AGGTCAGGAGATCGA | 25929 |
| rs192531794 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154921522 | GTCCCCATTATAAAC[A/C]TAACTACTAATAATT | 25929 |
| rs192534727 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154902411 | TAGTTTGTCTATTGC[C/T]GTCTATTGCTTTGTA | 25929 |
| rs192574870 | snp | A/C/G | 0.000177841 | 0.00942809 | utr-variant-5-prime | GEMIN5 | GRCh38.p7 | 5:154938177 | CTGCCACAGCCGACC[A/C/G]CTCGTAGCCTCACGC | 25929 |
| rs192753545 | snp | A/C/G | 3.3172e-05 | 0.00407248 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154924474 | CATTTCTTACTTGTT[A/C/G]GAGTAGGTGTCATAC | 25929 |
| rs192796725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154893053 | GGTGAGCTGAGATTG[C/T]GCCACTGCACTCCAG | 25929 |
| rs192811506 | snp | A/G | 0.030665 | 0.119967 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154929141 | AGGCAGGAGAATGGC[A/G]TGAACCCAGGAGGTG | 25929 |
| rs192882205 | snp | G/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154920977 | TAGATATTATTCCAT[G/T]AATATACTGAAGTAT | 25929 |
| rs192959952 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154905678 | CTAGCTGTTTTCAGG[A/T]ATCTGTAAGTCTATT | 25929 |
| rs193001256 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154915687 | GAAAATGAGGATAAC[A/G]TTACCTATCACCCTC | 25929 |
| rs193072914 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154931948 | AACCCGGGAGGCGGA[C/G]GTTGCGGTGAGCCGA | 25929 |
| rs193124566 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154892776 | GTCTGTTCACACTGA[A/G]AAAACACCTTTACAT | 25929 |
| rs193180838 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154933532 | TAAGACAATTTCAGG[C/T]TTGATGACTAGTAAT | 25929 |
| rs193235026 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154914303 | CGGGATTATAGGCGT[A/G]AGCCACCACGCCCGG | 25929 |
| rs193240052 | snp | A/G | 0.00159617 | 0.0282053 | downstream-variant-500B | GEMIN5 | GRCh38.p7 | 5:154886930 | TGGTAACAAAGCATC[A/G]TCTTCCTAAAGTTCA | 25929 |
| rs193262678 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | GEMIN5 | GRCh38.p7 | 5:154938738 | AAACAAAAATAAAAT[A/G]AAATAATAAAATAAG | 25929 |
| rs193276341 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154910931 | CTCGGATCTCCCGAC[C/T]TTGTGATCCGCCCAT | 25929 |
| rs199593329 | in-del | -/G | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154905699 | TAAGTCTATTACTTT[-/G]GTTTTTTTTTTTTTT | 25929 |
| rs199596248 | snp | C/T | 3.30251e-05 | 0.00406343 | missense | GEMIN5 | GRCh38.p7 | 5:154903098 | CAATATCAATCATTC[C/T]ATACAGGGTAGCCCT | 25929 |
| rs199624835 | snp | C/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154896695 | CTGGGCTCATCAGGT[C/T]CTTTCTCCCTGACCA | 25929 |
| rs199636427 | snp | A/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154899620 | ATGTGCTTTTTTATT[A/T]AAAAAAAAAAAATGT | 25929 |
| rs199661588 | snp | C/G | 1.64789e-05 | 0.0028704 | missense | GEMIN5 | GRCh38.p7 | 5:154898520 | CTTGGGCACATCTGA[C/G]AGCCAGGGAAGCAGA | 25929 |
| rs199675993 | in-del | -/T | 0.0150606 | 0.0854603 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154904147 | AATAAGAAAAAAAGA[-/T]TTTTTTCTCCATAGG | 25929 |
| rs199704979 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154924782 | ATCACGAGGTCAGGA[C/G]ATCGAGACCATCCTG | 25929 |
| rs199746622 | snp | A/C/T | 0.000264155 | 0.0114896 | synonymous-codon, missense | GEMIN5 | GRCh38.p7 | 5:154927520 | TTTCCGTCTCCAAGA[A/C/T]TGAGTGAGATCCCAT | 25929 |
| rs199767655 | snp | G/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154897915 | GTGTTTTTTTTTGTG[G/T]TTTTTTTTTTTTTTT | 25929 |
| rs199773726 | snp | A/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154907456 | GACTTGAATAAAGCT[A/T]AACAAAAAAAACTAA | 25929 |
| rs199779850 | snp | C/G | 0.000149732 | 0.00865121 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154931600 | ATAGGTGGCAATTTT[C/G]TTTTTAATTTACATT | 25929 |
| rs199843544 | snp | G/T | 0.000116058 | 0.0076168 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154898416 | TTCCCTCTTGTATAC[G/T]AGGAGATGAAATAAC | 25929 |
| rs199873728 | snp | C/T | 0.00199792 | 0.0315431 | missense | GEMIN5 | GRCh38.p7 | 5:154896168 | GCTTCCTGATACTGC[C/T]CAGGGGTGTCAAGGC | 25929 |
| rs199906317 | in-del | -/A | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154910314 | TCTTTCATTTAAAAT[-/A]AAAAAAAAACTTATT | 25929 |
| rs199925919 | in-del | -/TGT | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154895048 | ATGCCACTGTACTCC[-/TGT]AGCCTGAGCAACAAG | 25929 |
| rs199930435 | snp | C/T | 8.24559e-05 | 0.00642037 | missense | GEMIN5 | GRCh38.p7 | 5:154907788 | TTAGGTTGAGAGAGC[C/T]GTTTTTTCTCCAATT | 25929 |
| rs199934995 | snp | A/G | 0.00014832 | 0.00861035 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154898557 | ATCCTCTCCTACGAT[A/G]GCAGCCAACTCTGCA | 25929 |
| rs199945289 | snp | C/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154917501 | CTTGATAAAATTGTG[C/T]TCATCAGGCATTAAT | 25929 |
| rs199960786 | snp | A/C/G | 6.59266e-05 | 0.00574106 | missense | GEMIN5 | GRCh38.p7 | 5:154907620 | CCACAGGGTAATTCC[A/C/G]GCTCCCGTGCTTGCT | 25929 |
| rs200003670 | snp | C/G/T | 4.95228e-05 | 0.00497588 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154904652 | TTAATAAAGTACATA[C/G/T]TATCTGAAGGAGAAC | 25929 |
| rs200020649 | in-del | -/A | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154903825 | TTTGAAAAAAAAATT[-/A]AAAAAAAAATTTTTT | 25929 |
| rs200023763 | snp | C/G | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154900885 | ATCAAAATGTAGGAG[C/G]TAATTCTAGAATATG | 25929 |
| rs200055716 | snp | A/C/G/T | 0.000247907 | 0.0111312 | missense | GEMIN5 | GRCh38.p7 | 5:154899278 | ACTGGGTCCTCCGGG[A/C/G/T]GCAGCCGGGCCTTGG | 25929 |
| rs200092874 | snp | A/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154895555 | ACAAGAAGGACTTCA[A/T]CTTTGCCCTACTGTT | 25929 |
| rs200098033 | snp | C/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154901796 | GTGCTTTTTTTTTTT[C/T]CCTTTCCTTTTATTG | 25929 |
| rs200100728 | in-del | -/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154916054 | AACTGTTTTTTTTTT[-/T]AATTTTTATTTTTTG | 25929 |
| rs200123085 | in-del | -/TGGGCATGG | 0.00517822 | 0.0506191 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154927847 | ATTAAAAAAATTAGT[-/TGGGCATGG]TGGTGCACATCTATG | 25929 |
| rs200127873 | snp | A/G | 0.000642562 | 0.0179128 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154898554 | CTCATCCTCTCCTAC[A/G]ATGGCAGCCAACTCT | 25929 |
| rs200155277 | snp | A/G | 0.00199806 | 0.0315443 | missense | GEMIN5 | GRCh38.p7 | 5:154927440 | TCCTCTGTTTGTAAA[A/G]GACATAAATTAAACA | 25929 |
| rs200204844 | snp | G/T | 1.72883e-05 | 0.00294004 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154905339 | CTTTAACAAAATACT[G/T]TATTTTAATTACTAG | 25929 |
| rs200206273 | snp | C/T | 0.000248602 | 0.0111463 | missense | GEMIN5 | GRCh38.p7 | 5:154891652 | CAGAATTCATACAGA[C/T]GCCCATAAAGAAAAA | 25929 |
| rs200211713 | snp | A/G/T | 1.65012e-05 | 0.00287234 | missense | GEMIN5 | GRCh38.p7 | 5:154921375 | ACTGGTGGCCCCCAG[A/G/T]CTAAAGTATATACAG | 25929 |
| rs200216146 | snp | A/G | 0.00199792 | 0.0315431 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154896326 | TAGCTCCAGAAGGCA[A/G]AACACCAATCTCTGA | 25929 |
| rs200227178 | snp | C/T | 6.58913e-05 | 0.00573945 | missense | GEMIN5 | GRCh38.p7 | 5:154907693 | AGTTCTCCTTCATGC[C/T]TTCTTCTTCATTTCC | 25929 |
| rs200274876 | snp | G/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154921933 | ATATGTGATGTGTCA[G/T]TAAAGAATGCTTAAC | 25929 |
| rs200282409 | snp | A/C | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154922318 | GACTACAGGCACCTG[A/C]CACCAAGCCCGGCTA | 25929 |
| rs200376323 | snp | C/G/T | 6.5931e-05 | 0.00574125 | missense | GEMIN5 | GRCh38.p7 | 5:154891611 | CCCAGACACTGGAAT[C/G/T]TGGGCAAGGTCTGGA | 25929 |
| rs200392401 | snp | C/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154902680 | AGTGACCTTTTCCTG[C/T]TTGAAAGAGAGATAA | 25929 |
| rs200397120 | snp | C/T | 3.31406e-05 | 0.00407053 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154899298 | CCGGGCCTTGGCAAT[C/T]GCAATAGCTTCCCTA | 25929 |
| rs200425177 | snp | C/T | 0.000329533 | 0.0128319 | missense | GEMIN5 | GRCh38.p7 | 5:154888341 | TGATGAGAAGCAGGA[C/T]GAGGCAGCACTCCAG | 25929 |
| rs200450703 | snp | A/T | 0.000181316 | 0.00951973 | missense | GEMIN5 | GRCh38.p7 | 5:154907779 | GGCTTTGCCTTAGGT[A/T]GAGAGAGCCGTTTTT | 25929 |
| rs200453473 | snp | G/T | 0.00155621 | 0.0278511 | missense | GEMIN5 | GRCh38.p7 | 5:154891257 | ACTGGCTCTGAGAAC[G/T]GCAGAGGGGCTGCTC | 25929 |
| rs200476714 | snp | A/G | 0.000280087 | 0.0118307 | missense | GEMIN5 | GRCh38.p7 | 5:154907627 | GTAATTCCGGCTCCC[A/G]TGCTTGCTCCTCCCC | 25929 |
| rs200552475 | snp | A/G | 0.0006931 | 0.0186029 | missense | GEMIN5 | GRCh38.p7 | 5:154891694 | CTTTTGAAAGCTGGT[A/G]TGGCAGGGGATTGAT | 25929 |
| rs200564666 | snp | A/G | 6.62164e-05 | 0.00575359 | missense | GEMIN5 | GRCh38.p7 | 5:154925863 | AAAAGAATCCTTACC[A/G]CTGTAACCTTGGACT | 25929 |
| rs200581237 | in-del | -/A | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154907459 | TGAATAAAGCTTAAC[-/A]AAAAAAAACTAATGC | 25929 |
| rs200600800 | in-del | -/ACC | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154909557 | TACAAAGTACCTACC[-/ACC]ACCACAATTACTTTT | 25929 |
| rs200609065 | snp | C/T | 0.00139503 | 0.0263736 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154931406 | GAACAGAAAACCCTC[C/T]ACTTCCACCAGATCA | 25929 |
| rs200624118 | in-del | -/ATT | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154915894 | ATTTTCTATACAAAA[-/ATT]ATTCATTCATGTTCA | 25929 |
| rs200628327 | in-del | -/AAATA | 0.0263992 | 0.111815 | upstream-variant-2KB | GEMIN5 | GRCh38.p7 | 5:154939054 | GCGAGACTCCATCTC[-/AAATA]AAAACAAAACAAAAC | 25929 |
| rs200632097 | snp | G/T | | | missense | GEMIN5 | GRCh38.p7 | 5:154892426 | CTTCCTGCATGATGG[G/T]GAAGCTCCCTGAGTC | 25929 |
| rs200669769 | snp | A/G | 0.000248281 | 0.0111391 | missense | GEMIN5 | GRCh38.p7 | 5:154905378 | CTGGCTTCTCTTTTG[A/G]TGGCTCCTTTTTCAG | 25929 |
| rs200680023 | snp | A/G | 0.000115307 | 0.00759211 | missense | GEMIN5 | GRCh38.p7 | 5:154891403 | CTCTGTGAGTTTTGG[A/G]GACTGGCATGCTTTT | 25929 |
| rs200714210 | snp | A/C | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154896708 | GTTCTTTCTCCCTGA[A/C]CAAACTTTGGACTCA | 25929 |
| rs200803533 | snp | A/G | 1.67307e-05 | 0.00289224 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154903042 | ATGTTGGGAAAGTAT[A/G]AAGATGGATGAGATT | 25929 |
| rs200832476 | in-del | -/ATAAA | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154921006 | ATCATTCTAATTCTG[-/ATAAA]ATTAAAAAGAGACAG | 25929 |
| rs200833094 | snp | A/G | 0.000165382 | 0.00909196 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154919958 | TACTTCAGGACCACA[A/G]GAACTCACTTTGATT | 25929 |
| rs200857874 | snp | A/G | 6.59174e-05 | 0.00574059 | missense | GEMIN5 | GRCh38.p7 | 5:154891286 | TCTGCTTCTACTTCC[A/G]GTTCATTCTTATCAG | 25929 |
| rs200876867 | snp | A/G | 1.6473e-05 | 0.00286988 | stop-gained | GEMIN5 | GRCh38.p7 | 5:154891401 | TTCTCTGTGAGTTTT[A/G]GAGACTGGCATGCTT | 25929 |
| rs200884806 | snp | C/T | 6.67512e-05 | 0.00577678 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154907857 | TGACTAAAGTATACA[C/T]TCTTGGTTAAAAGCA | 25929 |
| rs200899956 | in-del | -/CTA | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154905959 | CCTCCCAAACTGCTG[-/CTA]GGATTACAGGCGTGA | 25929 |
| rs200903180 | snp | A/G | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154925176 | ATACACTGTCGAGTC[A/G]GAATAAGAGATTCTG | 25929 |
| rs200907595 | snp | A/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154916055 | AACTGTTTTTTTTTT[A/T]ATTTTTATTTTTTGT | 25929 |
| rs200916098 | snp | C/G/T | 0.00199792 | 0.0315431 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154899173 | TGTTGGAAGCATCCC[C/G/T]CCACTCCTCAGGCTT | 25929 |
| rs200933400 | snp | A/G | 3.42513e-05 | 0.00413817 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154892562 | GAGCTGGAGAGAGAA[A/G]CCAGAGTCTGAGTTA | 25929 |
| rs200970864 | snp | G/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154895728 | TATTTTACTTTTTTA[G/T]AAAAGGAAATAGTGG | 25929 |
| rs200988055 | in-del | -/TCTTGTT | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154895049 | TGCCACTGTACTCCA[-/TCTTGTT]GCCTGAGCAACAAGA | 25929 |
| rs200989740 | snp | C/T | 1.65012e-05 | 0.00287234 | missense | GEMIN5 | GRCh38.p7 | 5:154921376 | CTGGTGGCCCCCAGG[C/T]TAAAGTATATACAGT | 25929 |
| rs200994174 | snp | C/G | 1.65825e-05 | 0.00287941 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154898415 | CTTCCCTCTTGTATA[C/G]TAGGAGATGAAATAA | 25929 |
| rs200994747 | snp | A/T | 1.64727e-05 | 0.00286986 | missense | GEMIN5 | GRCh38.p7 | 5:154896126 | TTTGTAGCAGATGGG[A/T]ACTTGATGTTCTGCA | 25929 |
| rs200999038 | snp | A/T | 8.24735e-05 | 0.00642106 | missense | GEMIN5 | GRCh38.p7 | 5:154917089 | CTGGCTGCCATGCTC[A/T]TGATGCCAGCTAATG | 25929 |
| rs201110168 | snp | G/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154927621 | ACTGTTGAGACAGAG[G/T]CTGGGCTCATAGCTG | 25929 |
| rs201137545 | snp | C/T | 0.000827226 | 0.0203206 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154917895 | CAAATATATGTGCGA[C/T]TGCAAATTTTTTATC | 25929 |
| rs201151742 | snp | A/C | 0.000399281 | 0.0141238 | missense | GEMIN5 | GRCh38.p7 | 5:154920008 | GTTTGTTGATGTCAA[A/C]GGCTTCTCCACTAAG | 25929 |
| rs201252889 | snp | A/C | 0.00199792 | 0.0315431 | missense | GEMIN5 | GRCh38.p7 | 5:154925891 | ACTTCACGCCTTGCC[A/C]AAAATTTTTCACATC | 25929 |
| rs201255197 | in-del | -/AT | 0.0138799 | 0.0821421 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154893518 | TGTAGTTTGAGAAAC[-/AT]ATATAGTTACAACAC | 25929 |
| rs201278136 | in-del | -/TTTCTCCCTG | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154896697 | GGGCTCATCAGGTTC[-/TTTCTCCCTG]ACCAAACTTTGGACT | 25929 |
| rs201303618 | snp | C/T | 3.29484e-05 | 0.00405871 | missense | GEMIN5 | GRCh38.p7 | 5:154891298 | TCCGGTTCATTCTTA[C/T]CAGGACCATTTGCTG | 25929 |
| rs201313338 | snp | A/C | 0.000399281 | 0.0141238 | missense | GEMIN5 | GRCh38.p7 | 5:154896265 | TGTGGTAAGAGGAGG[A/C]GCTTTTGCCCTCTGA | 25929 |
| rs201322220 | snp | A/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154907455 | AGACTTGAATAAAGC[A/T]TAACAAAAAAAACTA | 25929 |
| rs201340849 | snp | A/G | 1.6534e-05 | 0.00287519 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154931580 | ATTTCAGCTTCTTCT[A/G]TGAGATAGGTGGCAA | 25929 |
| rs201344739 | in-del | -/A | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154913816 | GTGAGACCCTGTCTC[-/A]AAAAAAAAAGGAAAA | 25929 |
| rs201349678 | snp | A/G | 3.30213e-05 | 0.00406319 | missense | GEMIN5 | GRCh38.p7 | 5:154912957 | TGATGTGGGCTCCAC[A/G]CCACACTGGTAATCT | 25929 |
| rs201367883 | snp | A/C | 0.000154827 | 0.00879712 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154912854 | AAGAAAGAATTTGTT[A/C]GAGTACACAGTGAAG | 25929 |
| rs201386340 | snp | C/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154893786 | TCTTGCTCTGTCGCC[C/T]AGGCTGGAGTGCAGT | 25929 |
| rs201406985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154904686 | TCAGAAACATAAAAC[A/G]GAATGCCTATTGTGT | 25929 |
| rs201459629 | in-del | -/G | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154897913 | GGTGTTTTTTTTTGT[-/G]GTTTTTTTTTTTTTT | 25929 |
| rs201557884 | snp | C/T | 0.000132888 | 0.00815024 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154924461 | AAGAAGAATCACCCA[C/T]TTCTTACTTGTTGGA | 25929 |
| rs201626285 | snp | C/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154896822 | TCCAAATAGGTTTAA[C/T]AGAGGAAGCTGGCTG | 25929 |
| rs201636706 | in-del | -/C | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154908171 | ATTTTACCCAGATGT[-/C]CTTTTTTTTTTTTTT | 25929 |
| rs201693545 | in-del | -/A | 0.00835141 | 0.0640778 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154918070 | CAATGACAGCATGAG[-/A]AAAAAAAAATCCCTA | 25929 |
| rs201702974 | snp | A/C | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154922324 | AGGCACCTGCCACCA[A/C]GCCCGGCTAATTTTT | 25929 |
| rs201813556 | snp | C/G | 1.64779e-05 | 0.00287031 | missense | GEMIN5 | GRCh38.p7 | 5:154931520 | CCAGTGGCTAAGTAG[C/G]AACCTTTTGTTACTG | 25929 |
| rs201862403 | snp | G/T | 0.000186348 | 0.00965087 | missense | GEMIN5 | GRCh38.p7 | 5:154937976 | GAGTTACCTCGAAAC[G/T]GGGGTGTCCCTGGAC | 25929 |
| rs201870712 | snp | A/G | 1.68587e-05 | 0.00290329 | stop-gained | GEMIN5 | GRCh38.p7 | 5:154935992 | TTAAGTCCTTTACTC[A/G]AGGAGACCAATGTAA | 25929 |
| rs201880938 | snp | C/T | 0.000399281 | 0.0141238 | missense | GEMIN5 | GRCh38.p7 | 5:154927509 | AAGAGGGTGTATTTC[C/T]GTCTCCAAGATTGAG | 25929 |
| rs201896089 | snp | A/G | 0.000728523 | 0.0190717 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154892552 | TGTGAAGCAGGAGCT[A/G]GAGAGAGAAGCCAGA | 25929 |
| rs201914166 | snp | A/C | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154896709 | TTCTTTCTCCCTGAC[A/C]AAACTTTGGACTCAG | 25929 |
| rs201931739 | in-del | -/GA | 0.221141 | 0.248329 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154895335 | CCAGTCTCCAGAAAG[-/GA]GAAAAAAAAAAAAAA | 25929 |
| rs201982564 | snp | C/G | 0.000399281 | 0.0141238 | missense | GEMIN5 | GRCh38.p7 | 5:154913002 | GAGAGGGTCCGGTAG[C/G]GCTCTGTAATGGTCA | 25929 |
| rs202041170 | snp | A/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154916057 | CTGTTTTTTTTTTAA[A/T]TTTTATTTTTTGTAT | 25929 |
| rs202062416 | snp | A/G | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154900884 | TATCAAAATGTAGGA[A/G]GTAATTCTAGAATAT | 25929 |
| rs202145813 | snp | A/G | 3.31455e-05 | 0.00407083 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154931441 | AGGTTACATCACAAA[A/G]GAAAGATCAATCTTA | 25929 |
| rs202177991 | snp | A/G | 0.000397272 | 0.0140882 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154931446 | ACATCACAAAAGAAA[A/G]ATCAATCTTACCTCG | 25929 |
| rs267600505 | snp | A/G | 1.64762e-05 | 0.00287016 | GEMIN5 | 5 | allele_origin=G(germline)/A(somatic) | 5:154925943 | TGTATTCCATACACG[A/G]ATCATGCCATCCCCA | 25929 |
| rs367582501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154905634 | CTGGAAAAGAAGTAG[A/G]AGTAGTTTCCCCTTT | 25929 |
| rs367583783 | snp | C/T | 9.94019e-05 | 0.00704919 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154921313 | GGAAGAATACTCTCA[C/T]ATTTGTTATGGAATT | 25929 |
| rs367596811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154928746 | ATAACACACAGTCTG[C/T]GCTGTAAAAGCTTGT | 25929 |
| rs367603305 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154905086 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 25929 |
| rs367607150 | snp | A/G | 0.000197661 | 0.00993939 | missense | GEMIN5 | GRCh38.p7 | 5:154891445 | TCCTTAAAAGTACTC[A/G]GCATTCGCTCACCTT | 25929 |
| rs367615644 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | MRPL22, GEMIN5 | GRCh38.p7 | 5:154939412 | GGGGCTTTGGGTGCT[A/G]TCAATCAGACGAATT | 25929 |
| rs367634594 | snp | A/G | 1.64917e-05 | 0.00287151 | missense | GEMIN5 | GRCh38.p7 | 5:154907789 | TAGGTTGAGAGAGCC[A/G]TTTTTTCTCCAATTC | 25929 |
| rs367638694 | snp | A/T | 3.4064e-05 | 0.00412684 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154937217 | ACGCTAGGTTAATCG[A/T]AGTGCTATCCAAGGT | 25929 |
| rs367648896 | snp | C/T | 6.59946e-05 | 0.00574395 | missense | GEMIN5 | GRCh38.p7 | 5:154925882 | TAACCTTGGACTTCA[C/T]GCCTTGCCAAAAATT | 25929 |
| rs367650268 | snp | C/T | 0.000165366 | 0.00909151 | missense | GEMIN5 | GRCh38.p7 | 5:154899284 | TCCTCCGGGCGCAGC[C/T]GGGCCTTGGCAATCG | 25929 |
| rs367672755 | snp | C/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154914920 | TGTTGAATCTATTAA[C/T]AGGAAAAAGTATATG | 25929 |
| rs367723986 | snp | A/T | 4.95782e-05 | 0.00497862 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154917904 | GTGCGATTGCAAATT[A/T]TTTATCTTAAAGAAG | 25929 |
| rs367740851 | snp | A/G | 8.28617e-05 | 0.00643615 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154898419 | CCTCTTGTATACTAG[A/G]AGATGAAATAACAGA | 25929 |
| rs367742193 | in-del | -/ATTTA | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154925380 | TTTTAAACCATAAAA[-/ATTTA]TTACCTTTAGATTCA | 25929 |
| rs367753782 | snp | C/T | 6.60786e-05 | 0.0057476 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154904668 | TATCTGAAGGAGAAC[C/T]GATCAGAAACATAAA | 25929 |
| rs367826335 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154900899 | GGTAATTCTAGAATA[C/T]GATAAACTTGCCCTA | 25929 |
| rs367934163 | in-del | -/C | 0.0115144 | 0.0749975 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154892751 | GCAGCACACACACGT[-/C]CCGGTGTTAAAGTCT | 25929 |
| rs367979011 | snp | A/C/G | 0.000108107 | 0.0073514 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154898668 | ATAATATGAATAAAA[A/C/G]TGTGAAGAAAATGTC | 25929 |
| rs368015403 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | GEMIN5 | GRCh38.p7 | 5:154938764 | ATAAGCCGGGTGTGG[C/T]GGCAGGCGCCTGTAA | 25929 |
| rs368045491 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154919535 | AGAAAATTAAAAACA[A/T]AATGACAATTTTGTC | 25929 |
| rs368088395 | snp | A/G | | | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154891678 | AAAAAAGGCCTCCAA[A/G]CTTTTGAAAGCTGGT | 25929 |
| rs368132978 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154921729 | CCAGAACATATATTA[C/T]CACCACCCAAATGTA | 25929 |
| rs368144941 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154924772 | AGGCGGGCGGATCAC[A/G]AGGTCAGGAGATCGA | 25929 |
| rs368181189 | snp | A/C | 1.75987e-05 | 0.00296631 | missense | GEMIN5 | GRCh38.p7 | 5:154936007 | GAGGAGACCAATGTA[A/C]TGTTGATATCGTATG | 25929 |
| rs368184251 | snp | A/G | 1.64836e-05 | 0.0028708 | missense | GEMIN5 | GRCh38.p7 | 5:154898576 | GCCAACTCTGCAGCC[A/G]TTCTAAGTGATGCCG | 25929 |
| rs368187222 | snp | A/G | 0.000131802 | 0.00811688 | missense | GEMIN5 | GRCh38.p7 | 5:154891526 | GAAGTTTCAGGGTCC[A/G]TTTCTTCAGTGCTGG | 25929 |
| rs368216471 | snp | C/G | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154900605 | AAACCTCAGCAGTCT[C/G]TGAGTTGAGAAGAGG | 25929 |
| rs368285231 | snp | C/T | 1.7416e-05 | 0.00295088 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154891215 | GGTCATTTTTCATTC[C/T]GTCTTGTACTTGCCT | 25929 |
| rs368298943 | in-del | -/CA | 0.00279162 | 0.0372561 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154917804 | ATCAGCGGAGGATAT[-/CA]AGAATAAATCAAAAT | 25929 |
| rs368304207 | snp | A/C/T | 8.24021e-05 | 0.00641834 | missense | GEMIN5 | GRCh38.p7 | 5:154919998 | TCCCTGATGAGTTTG[A/C/T]TGATGTCAAAGGCTT | 25929 |
| rs368313399 | snp | A/G | 6.67334e-05 | 0.00577601 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154903204 | AAGGCAAAAAAATCA[A/G]ATGAAGTCATTACAT | 25929 |
| rs368324229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154902274 | CAGACTTGTGCCATT[A/G]TATCTTTTAAAATTT | 25929 |
| rs368350644 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154929943 | CATGGAAGCAACCCA[A/C]ATGTCCATCAGTGTG | 25929 |
| rs368402790 | snp | G/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154905717 | TTTTTTTTTTTTTTT[G/T]AGACGAAGTCTCACT | 25929 |
| rs368495107 | snp | C/T | 3.93941e-05 | 0.00443796 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154937960 | CGGGCCCAAGGGTGG[C/T]GAGTTACCTCGAAAC | 25929 |
| rs368518901 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154908225 | CGCTCTTCTTGCCCC[A/G]GCGGGAGTGCAATGG | 25929 |
| rs368523686 | snp | A/G/T | 6.59135e-05 | 0.00574047 | missense, synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154937127 | GTTGTACTGACCAGG[A/G/T]TGATGAGAAAATGTG | 25929 |
| rs368662572 | snp | A/G | 1.64727e-05 | 0.00286986 | missense | GEMIN5 | GRCh38.p7 | 5:154904536 | GCAGTTGCTAGTACC[A/G]AACAGTCCTGATGAA | 25929 |
| rs368700438 | snp | C/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154927757 | AGCATTCTAGGAGGC[C/T]AAGGCAGGAGGATTG | 25929 |
| rs368801791 | snp | A/C | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154900305 | AACATAAAGTTGTAG[A/C]TGGGAAAAAAGTGTT | 25929 |
| rs368853764 | snp | A/G | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154931370 | TGCTCTCAAATAGAT[A/G]ACACACCCTCAGGAC | 25929 |
| rs368855627 | snp | G/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154906048 | TTGCCCAGGCTGGAG[G/T]GCAGTGGGTGCAATC | 25929 |
| rs368867908 | snp | A/G | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154911570 | ATTGTGGGTGGTGTT[A/G]TTCTCAAGCCCTTGT | 25929 |
| rs368877922 | in-del | -/T/TT/TTT | 0.499653 | 0.0131743 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154897914 | GTGTTTTTTTTTGTG[-/T/TT/TTT]TTTTTTTTTTTTTTT | 25929 |
| rs368904483 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | GEMIN5 | GRCh38.p7 | 5:154938194 | TCGTAGCCTCACGCC[G/T]TAGGTAGGGAGCGGG | 25929 |
| rs368927983 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154918422 | TATGCTGGTATTCCC[C/G]AAGGCTGCCTGGGCC | 25929 |
| rs368945383 | snp | A/G | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154893783 | GAGTCTTGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 25929 |
| rs368952814 | snp | A/G | 4.96372e-05 | 0.00498158 | missense | GEMIN5 | GRCh38.p7 | 5:154892470 | ACCGCCCGAAGGAGC[A/G]CCTGCACAGCCTCGT | 25929 |
| rs368975512 | snp | A/C | 0.000153988 | 0.00877328 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154912892 | AGGGACAAGGACACA[A/C]TAGTACCTGGGCTGT | 25929 |
| rs369002208 | snp | A/G | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154916648 | ATGCACCTCTAACCC[A/G]GCAAATTTGTTTTTT | 25929 |
| rs369018916 | in-del | -/TAGAA | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154934937 | TCAGAAATACCAGAA[-/TAGAA]CACCTTTTTCTTCCA | 25929 |
| rs369039638 | snp | A/C | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154923702 | TCTTAATTCATGGAC[A/C]ATGGTTCACCAACGC | 25929 |
| rs369052797 | snp | C/T | 0.00014858 | 0.00861788 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154912956 | ATGATGTGGGCTCCA[C/T]GCCACACTGGTAATC | 25929 |
| rs369111911 | snp | A/G/T | 3.57924e-05 | 0.00423027 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154905520 | AAGTTAAGGATAACA[A/G/T]TAATACAGAATTTCA | 25929 |
| rs369129323 | snp | C/G/T | 8.23627e-05 | 0.0064168 | missense | GEMIN5 | GRCh38.p7 | 5:154928590 | AGTGTCAACCAAAGG[C/G/T]GCTCTTTAACAGTTG | 25929 |
| rs369151963 | snp | C/T | 3.31208e-05 | 0.00406931 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154901288 | ATAGAGAAGTTTAGG[C/T]TATTTTCACATTATG | 25929 |
| rs369154548 | snp | A/G | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154928017 | AAAATTTAATCACAG[A/G]AAGGGGAACCAAGTA | 25929 |
| rs369180681 | snp | C/T | 9.77804e-05 | 0.00699147 | missense | GEMIN5 | GRCh38.p7 | 5:154938058 | CGAAGCCAAAGAGGC[C/T]CCCGGGCACGGCATC | 25929 |
| rs369256553 | snp | A/G | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154913298 | AGCCTCCCAAGTCTA[A/G]GTGATTTTTAGCAGG | 25929 |
| rs369355255 | snp | C/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154908538 | ACATGGTACATTTGG[C/T]TGCCATGCCTTTCTG | 25929 |
| rs369393626 | snp | C/T | 1.65274e-05 | 0.00287462 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154902507 | AGATGATAGAGCTTT[C/T]GTTGAAAAGAACAAA | 25929 |
| rs369415207 | snp | C/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154926350 | TGTCTCCAAGTTCGG[C/T]GGTCTTTCTGTCCTA | 25929 |
| rs369457262 | snp | C/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154902969 | CCTAGTTAGCTGACA[C/T]GTAAAACTAACCATT | 25929 |
| rs369487086 | snp | A/G | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154908463 | TGGGATTACAGGCAT[A/G]AGCCACCACGCCCGG | 25929 |
| rs369487232 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154917838 | CAAATACAACTGGGC[C/G/T]GCCCCAGCTAACATT | 25929 |
| rs369491684 | snp | A/G | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154902359 | AATTAAAGTGTCAGT[A/G]ACCTGCTTTTTTTCA | 25929 |
| rs369512792 | snp | C/T | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154936462 | TTAGTAGTACTTCTA[C/T]AGCAACACGATATTA | 25929 |
| rs369542296 | snp | C/T | 9.91572e-05 | 0.00704051 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154905385 | CTCTTTTGGTGGCTC[C/T]TTTTTCAGTAAAATG | 25929 |
| rs369575481 | snp | C/T | 0.000166243 | 0.00911558 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154888386 | GCCAGGCCTGAAAGA[C/T]GATGACATGAGGATG | 25929 |
| rs369600670 | snp | A/G | 1.64803e-05 | 0.00287052 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154927493 | TTCTGATGAGGCACT[A/G]AAGAGGGTGTATTTC | 25929 |
| rs369608147 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-3-prime | GEMIN5 | GRCh38.p7 | 5:154887718 | CAGTCTATGAAAGAG[C/T]AGAGAGAGAAGGGTC | 25929 |
| rs369654948 | snp | A/G | 1.64836e-05 | 0.0028708 | synonymous-codon | GEMIN5 | GRCh38.p7 | 5:154926039 | GGAAGGAAGGGTCCA[A/G]CTGCACTCCAAGGTG | 25929 |
| rs369688044 | snp | A/G | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154924931 | GAGGCGGAGCTTGCA[A/G]TGAGCCGAGATTGTG | 25929 |
| rs369689700 | snp | A/G | | | intron-variant | GEMIN5 | GRCh38.p7 | 5:154908370 | ATTTTCAGTAGAGAC[A/G]GGGTTTCACCATGTT | 25929 |
| rs369703460 | snp | A/C | 1.69487e-05 | 0.00291103 | intron-variant | GEMIN5 | GRCh38.p7 | 5:154888410 | GAGGATGAATAAGGA[A/C]GCATTTGCAGAAGAG | 25929 |