| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs76609010 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27923187 | AATGTGAATGCGTTT[A/T]ACTCATTAAAACAAA | 55130 |
| rs76609991 | snp | C/T | 0.111928 | 0.208413 | intron-variant | ARMC4 | GRCh38.p7 | 10:27888576 | TAGTCCCTTGTCGGA[C/T]ATGTACTTTGCAAAT | 55130 |
| rs76612016 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | ARMC4 | GRCh38.p7 | 10:27949737 | AAGATCACTCTGGCT[A/G]CAGAGGCCGCTGGCT | 55130 |
| rs76635670 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | ARMC4 | GRCh38.p7 | 10:27822713 | ATTTGCTGGCTGGAG[C/G]AAAACCTTTGGTTCT | 55130 |
| rs76669336 | snp | G/T | 0.111576 | 0.20818 | intron-variant | ARMC4 | GRCh38.p7 | 10:27888585 | GTCGGATATGTACTT[G/T]GCAAATATTTTCTCT | 55130 |
| rs76728224 | snp | A/G | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27909817 | AGTGAGTCTTCATTT[A/G]AAAAAAAAAAAAAAA | 55130 |
| rs76808616 | snp | C/G | 0.0341408 | 0.126114 | intron-variant | ARMC4 | GRCh38.p7 | 10:27917680 | ATTGTAGGCTTTGTA[C/G]GTAACATATAAGCTC | 55130 |
| rs76828681 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27858679 | TTTGGTCACTTTACA[C/T]GGTAGGATAATATTC | 55130 |
| rs76832534 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27849998 | GAACCCGAAGTTCCA[C/T]GAGTCACGGTTTGAA | 55130 |
| rs76836039 | snp | A/C/T | 0.0326228 | 0.12363 | intron-variant | ARMC4 | GRCh38.p7 | 10:27869922 | GGGAAGGGAGTGACA[A/C/T]CTCTAAGCTACTCAA | 55130 |
| rs76858530 | snp | A/G | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27886279 | AAGTGAAAAAAAAAA[A/G]CAACATGTCATGTAC | 55130 |
| rs76869636 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARMC4 | GRCh38.p7 | 10:27949599 | AAGGCCAGAGCCCAG[A/G]GTGGGAGCGTGGTGC | 55130 |
| rs76888639 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | ARMC4 | GRCh38.p7 | 10:27818416 | GTCTTGACTCCATTG[G/T]TATACAAAATATAGC | 55130 |
| rs76925533 | snp | C/T | 0.125874 | 0.217008 | intron-variant | ARMC4 | GRCh38.p7 | 10:27964550 | AAGAATGCTGTCTTT[C/T]GGTATCTTTGTTAAA | 55130 |
| rs76940048 | snp | G/T | 0.0614824 | 0.164198 | intron-variant | ARMC4 | GRCh38.p7 | 10:27919791 | TATGCAATACTAATC[G/T]ATAGTAATGGAAATA | 55130 |
| rs76957305 | snp | A/G | 0.111224 | 0.207945 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27982694 | TCCAGGCAGTCCCCC[A/G]TGATGGCTGGGTCCC | 55130 |
| rs76970342 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | ARMC4 | GRCh38.p7 | 10:27861385 | CAGTGCACTCAAAGG[G/T]GACCAAGCATCTGAC | 55130 |
| rs76981190 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ARMC4 | GRCh38.p7 | 10:27915151 | TAAAAACCACACCTA[C/T]ACACATCATAATCAA | 55130 |
| rs76992283 | snp | A/T | 0.0193772 | 0.0965046 | intron-variant | ARMC4 | GRCh38.p7 | 10:27919057 | GAAAGACCCAAATAA[A/T]TGGCAATATATACCT | 55130 |
| rs77007927 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ARMC4 | GRCh38.p7 | 10:27947259 | ATAAGCCAGTACTTC[C/T]ATTTCCTCTTTTAAA | 55130 |
| rs77009477 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | ARMC4 | GRCh38.p7 | 10:27926713 | AAGAAAGTAAAGATC[C/T]TGAGGTATGGAAAAA | 55130 |
| rs77028639 | snp | G/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872909 | TCTTTTTCTATTGTT[G/T]GGAATAGTTTCAGAA | 55130 |
| rs77033139 | snp | C/G | 0.22263 | 0.248497 | intron-variant | ARMC4 | GRCh38.p7 | 10:27949690 | TTTATTTCAAGATTG[C/G]CCAATGTAATTTACA | 55130 |
| rs77175919 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | ARMC4 | GRCh38.p7 | 10:27952645 | TTACCACAGGGAGAT[G/T]TAAAAGTCTATCAAT | 55130 |
| rs77192423 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ARMC4 | GRCh38.p7 | 10:27949311 | GAAAAAGGTTTTTAA[C/T]TTTTTTAAGCTCACC | 55130 |
| rs77227360 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | ARMC4 | GRCh38.p7 | 10:27826369 | TCTCTAATTTCCATC[A/G]GCTCTCCGTGTTGCC | 55130 |
| rs77228272 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27981348 | ATGTTGTAAAAAAAA[A/C]CCACTAATAATAAAA | 55130 |
| rs77230530 | snp | C/T | 0.137527 | 0.223271 | intron-variant | ARMC4 | GRCh38.p7 | 10:27949416 | GGAACTTTGACCTAA[C/T]TTGGAGCATCACTCA | 55130 |
| rs77242182 | snp | A/T | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27963026 | CTTTTTTTTTTTTTT[A/T]AGACGAGATCTCGCT | 55130 |
| rs77244952 | snp | C/G | 0.0283406 | 0.115616 | intron-variant | ARMC4 | GRCh38.p7 | 10:27827893 | GTTCATCTTTAGCTT[C/G]TCTTCTTTTTTCTGT | 55130 |
| rs77280977 | snp | A/G | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27941501 | CGAACCAAAAAAAAG[A/G]AAAAAAAAAAACCAT | 55130 |
| rs77371675 | snp | C/T | 0.0640965 | 0.167152 | intron-variant | ARMC4 | GRCh38.p7 | 10:27923580 | GTTCACACAAAATAA[C/T]AAGATAGAAGACATA | 55130 |
| rs77426693 | snp | C/G | 0.0818113 | 0.184966 | intron-variant | ARMC4 | GRCh38.p7 | 10:27830070 | GAAAGTAGGGCACAG[C/G]ATGGTGGAACTTAGC | 55130 |
| rs77441321 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | ARMC4 | GRCh38.p7 | 10:27821460 | TTGGGCTCAGGAATA[C/T]GTTTTCATTTTCCTA | 55130 |
| rs77447998 | snp | C/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27969513 | AACTCACTTGCCAGT[C/T]AAAAAAGTTGCCCAT | 55130 |
| rs77463607 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | ARMC4 | GRCh38.p7 | 10:27979421 | TTGTATGCAGAAAAA[C/T]CTAAGAATACACACA | 55130 |
| rs77483386 | snp | C/T | 0.0244538 | 0.107838 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27959921 | GAATATGTGACATAA[C/T]TATATTGCAACAACA | 55130 |
| rs77505784 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | ARMC4 | GRCh38.p7 | 10:27895671 | CACTGAATAGCCACA[C/T]GTGGCTAGTAGTTGC | 55130 |
| rs77509067 | snp | A/G | 0.0952156 | 0.196321 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984415 | CAGTTAATTTTAGCC[A/G]TGCTATAATTTTATA | 55130 |
| rs77516742 | snp | A/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27921831 | AGGCAATAGAGCAGT[A/T]TTTTATTTTTTTTTT | 55130 |
| rs77530863 | snp | C/T | 0.0460598 | 0.144597 | intron-variant | ARMC4 | GRCh38.p7 | 10:27860881 | ATGGGATCTGTGCAT[C/T]GTAATGACCCTGCAA | 55130 |
| rs77552996 | snp | C/T | 0.182614 | 0.240747 | intron-variant | ARMC4 | GRCh38.p7 | 10:27907317 | TCTCCCCCATGGCTG[C/T]ACTCTCTCTGGATAG | 55130 |
| rs77554877 | snp | C/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27902225 | GGTAAATAACGAAAT[C/T]AAGGCAGAAACAAAG | 55130 |
| rs77588773 | snp | C/T | 0.0930568 | 0.194599 | intron-variant | ARMC4 | GRCh38.p7 | 10:27994591 | ATATGTGTATATATA[C/T]CTCCACATATGGGTG | 55130 |
| rs77624365 | snp | A/G | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27902296 | CACACTGCTTTGAAT[A/G]TGTCCCATAGATTCT | 55130 |
| rs77627269 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | ARMC4 | GRCh38.p7 | 10:27915963 | TGGTCCACCATGGAG[G/T]GTTAGAGCACAAGAA | 55130 |
| rs77728719 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | ARMC4 | GRCh38.p7 | 10:27947047 | TTCAGAATGACAAGA[A/G]CCTTAATTTTACTAT | 55130 |
| rs77733114 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | ARMC4 | GRCh38.p7 | 10:27931740 | GATAACATTTAGAAG[A/G]AATTTCAAGGTGGCA | 55130 |
| rs77744242 | snp | A/G | 0.0271762 | 0.113356 | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27981890 | AGCTTCCTTCTCTCC[A/G]CTCTCCTCTACTCTG | 55130 |
| rs77784687 | snp | A/C | 0.5 | 0 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:28000854 | TTTTTCCTTGTCGTG[A/C]TGAAACACTACCTGG | 55130 |
| rs77816698 | snp | G/T | 0.0341408 | 0.126114 | intron-variant | ARMC4 | GRCh38.p7 | 10:27921695 | ATTCTGAGACAAACC[G/T]AGCAAAATTATTAGA | 55130 |
| rs77841606 | snp | A/C | 0.143622 | 0.226238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27840458 | TTGTGTTCCACCTCC[A/C]ATGGCAAGTCTTGGA | 55130 |
| rs77862527 | snp | C/G | 0.0341408 | 0.126114 | intron-variant | ARMC4 | GRCh38.p7 | 10:27971452 | TAACAGCTAAACAAG[C/G]ACAACATCAAGACTA | 55130 |
| rs77874990 | snp | A/G | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27941336 | TGGAAAAAAAAAAAA[A/G]AAGCTGGATGTGGTG | 55130 |
| rs77885800 | snp | A/C | 0.0667028 | 0.170006 | intron-variant | ARMC4 | GRCh38.p7 | 10:27925448 | CTACAGCCTCAAATT[A/C]CTGATCTCAAATAAT | 55130 |
| rs77908800 | snp | C/G | 0.0752113 | 0.178743 | intron-variant | ARMC4 | GRCh38.p7 | 10:27843626 | GAAAAAAATTAGCTG[C/G]GTGTGGTGGCATGTG | 55130 |
| rs77913232 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ARMC4 | GRCh38.p7 | 10:27886102 | GAGAAAAGGACAGGA[A/G]AATTATTTAAAGTAA | 55130 |
| rs77921988 | snp | C/T | 0.0681886 | 0.171594 | intron-variant | ARMC4 | GRCh38.p7 | 10:27957510 | GCAGAAGGCAGAACA[C/T]AAGTGCTTATCAGTA | 55130 |
| rs77927522 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | ARMC4 | GRCh38.p7 | 10:27826129 | CTATCAGAAATTCCA[C/G]GTTCTGGAGGACGCA | 55130 |
| rs77935083 | snp | G/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27820797 | TTTTTTTTTTTTTTT[G/T]TTTTGATGGAGTTTT | 55130 |
| rs77935856 | snp | G/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27873033 | AGACCAATAACAGGA[G/T]CTGAAATTGTGGCAA | 55130 |
| rs77977051 | snp | A/C | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27970445 | CTAGCATGATTTTTA[A/C]ATTTCCCCTGTGACT | 55130 |
| rs77996705 | snp | C/T | 0.0360663 | 0.129354 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984581 | ACTATACAAACTCTA[C/T]ATGATATCTGCATTA | 55130 |
| rs78030982 | in-del | -/AAA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27953803 | GCATATATGAGTGTG[-/AAA]CTATTTGTATAATAT | 55130 |
| rs78039087 | snp | A/G | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27922198 | GAAAAAAGAAAAAAA[A/G]AAAAGAAAACAACAA | 55130 |
| rs78060407 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27982497 | CTAATTAGAGATTTC[A/G]TTTTTCTAAAATATC | 55130 |
| rs78115355 | snp | A/G | 0.0592355 | 0.161582 | intron-variant | ARMC4 | GRCh38.p7 | 10:27914231 | ATCGAGAGGCACAAA[A/G]TATCTAGTTGTCCAA | 55130 |
| rs78244072 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | ARMC4 | GRCh38.p7 | 10:27990245 | CTCGAACTCCTGGGC[C/T]CAAGGGATTCTTCTC | 55130 |
| rs78251735 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | ARMC4 | GRCh38.p7 | 10:27992385 | CTCAGGAGGGAACAC[C/T]GTGCATAAAGACTGC | 55130 |
| rs78265374 | snp | A/G | 0.167158 | 0.235875 | intron-variant | ARMC4 | GRCh38.p7 | 10:27917816 | AAAAAAGAGACTGAT[A/G]GAGAGAGAGAAAAAT | 55130 |
| rs78278231 | snp | A/C | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27921736 | AAAAATCCCCAGTCC[A/C]AAAAAAAAAAAATCA | 55130 |
| rs78315667 | snp | A/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27921832 | GGCAATAGAGCAGTA[A/T]TTTATTTTTTTTTTT | 55130 |
| rs78322375 | in-del | -/AAAAAAA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27924634 | AAAAAAAAAAAAAAA[-/AAAAAAA]CAGAAGAAAGCCCAC | 55130 |
| rs78354914 | snp | A/C | 0.0341408 | 0.126114 | intron-variant | ARMC4 | GRCh38.p7 | 10:27924303 | TGGGCTAACAGGGGA[A/C]TACAAAGTGAAATTA | 55130 |
| rs78414228 | in-del | -/A | 0.218151 | 0.247963 | intron-variant | ARMC4 | GRCh38.p7 | 10:27907496 | CTGACCAGAAAAAAA[-/A]GCAATGCTCCGAAAT | 55130 |
| rs78431189 | snp | C/G | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27902314 | GCTATAAATTTCCCT[C/G]TACACACTGCTTTGA | 55130 |
| rs78455465 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27959491 | GCGTGGCCTAAATGT[C/T]CCAAAGCTGGGCATG | 55130 |
| rs78457752 | in-del | -/TA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27921835 | AATAGAGCAGTATTT[-/TA]TTTTTTTTTTTGTAA | 55130 |
| rs78492276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27884292 | ATTCTCCTATGGAAA[C/T]ATTAAATAAACAACT | 55130 |
| rs78539052 | snp | G/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27937356 | TTTTTTTTTTTTTTT[G/T]AGAGAGACTCTTGCT | 55130 |
| rs78543332 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | ARMC4 | GRCh38.p7 | 10:27966008 | GGGTTCTCGTCCATA[A/G]AAGTCTTTTCTGTTC | 55130 |
| rs78582348 | snp | A/C | 0.0667028 | 0.170006 | intron-variant | ARMC4 | GRCh38.p7 | 10:27946348 | CTTGTGCATTTGCAA[A/C]TCTTCTTGTGAATTC | 55130 |
| rs78611135 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27915576 | TGAGGGAACAGTATA[C/T]ATAGCACAGTAGGTA | 55130 |
| rs78614042 | snp | A/C | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27881467 | AGACTTCTGCTTCTA[A/C]AAAAAAAAAAAAATT | 55130 |
| rs78641598 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | ARMC4 | GRCh38.p7 | 10:27923136 | AATTATAAAAAATTA[C/T]GACATTGTTGAAACT | 55130 |
| rs78642722 | in-del | -/GAATAAAT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27970141 | AATAAATAAATAAAT[-/GAATAAAT]AAATAAATCTCTAGG | 55130 |
| rs78657710 | snp | G/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872998 | TCCTGGACTCTTTTT[G/T]GTTGGTAAACTATTG | 55130 |
| rs78680307 | snp | A/G | 0.277778 | 0.248452 | intron-variant | ARMC4 | GRCh38.p7 | 10:27929491 | CATTGTTTTGTCTTA[A/G]CTTAATATTTAAATG | 55130 |
| rs78682156 | snp | A/T | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872879 | GCCTCATAAAATGAG[A/T]TAGGGAGGATTCCCT | 55130 |
| rs78744932 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27873015 | GAAATTGTGGCAATA[A/G]TCAACAGCTTACCAA | 55130 |
| rs78772332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27850034 | CTAATCAAATGGACA[C/T]AGCACTAAAGTGAAT | 55130 |
| rs78784273 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | ARMC4 | GRCh38.p7 | 10:27817387 | AGGGTACAAGTGCAA[A/G]TTTCTTACATGCATA | 55130 |
| rs78833558 | in-del | -/G | 0.331874 | 0.236213 | intron-variant | ARMC4 | GRCh38.p7 | 10:27922330 | GAAGATTCTCCTAGA[-/G]GGATGAGCTCCAAAC | 55130 |
| rs78853350 | snp | A/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27829933 | TTCAGGCAGTAATTA[A/T]AAAAAAAAAAATGTA | 55130 |
| rs78891477 | snp | A/G | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27922190 | AAACAAAAGAAAAAA[A/G]AAAAAAAGAAAAGAA | 55130 |
| rs78900698 | snp | C/T | 0.167484 | 0.23599 | intron-variant | ARMC4 | GRCh38.p7 | 10:27925929 | GAGAATTGCTTGAGC[C/T]CGGGATGCAAGGGTT | 55130 |
| rs78909751 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ARMC4 | GRCh38.p7 | 10:27896765 | GTAGATATATGTATA[C/T]AGATATAGATATATA | 55130 |
| rs78922577 | snp | C/T | 0.143622 | 0.226238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27850835 | AGGTAAGCCCTAAGA[C/T]TGACCCAGACTAACT | 55130 |
| rs78936147 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27996889 | CCTATATATTCTAGT[A/G]TAGTGGTACTTGAGC | 55130 |
| rs78939776 | snp | C/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27961512 | AGCAGCATATACATC[C/T]TTGGGAAAGTATTTT | 55130 |
| rs78953108 | snp | A/C | 0.167484 | 0.23599 | intron-variant | ARMC4 | GRCh38.p7 | 10:27928819 | CCTACATTTACACAC[A/C]GCACTTATTATATGT | 55130 |
| rs79015389 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27908763 | GAGTTTACCAGGGGG[A/G]AAAAATGTATTATTC | 55130 |
| rs79036356 | snp | C/T | 0.0554779 | 0.157039 | intron-variant | ARMC4 | GRCh38.p7 | 10:27911613 | TCTCCCCGTTATGCA[C/T]TTTCAACTATTGCTG | 55130 |
| rs79110720 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27881314 | AAATATATAACTCAG[C/G]TAACAACAAACATTG | 55130 |
| rs79122761 | snp | A/G | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27820802 | TTTTTTTTTTTTTTT[A/G]ATGGAGTTTTCCTCC | 55130 |
| rs79132576 | snp | A/C | 0.0471551 | 0.14613 | intron-variant | ARMC4 | GRCh38.p7 | 10:27912004 | ATACTTGCAAAATAC[A/C]CGTTCAAATTCTAAA | 55130 |
| rs79146969 | snp | A/C | 0.031825 | 0.122064 | intron-variant | ARMC4 | GRCh38.p7 | 10:27885023 | AGATCTGAAGACATA[A/C]GAAGAAACAGGAAAG | 55130 |
| rs79169887 | snp | C/T | 0.138207 | 0.223612 | intron-variant | ARMC4 | GRCh38.p7 | 10:27863128 | CTGATTTCATATATA[C/T]TGTTCATTCATTCAT | 55130 |
| rs79200464 | snp | A/C | 0.0170251 | 0.090679 | intron-variant | ARMC4 | GRCh38.p7 | 10:27813359 | CAGTAGCAGTTTACT[A/C]AAATGTCTGTTGCTA | 55130 |
| rs79221009 | snp | C/T | 0.0876345 | 0.190099 | intron-variant | ARMC4 | GRCh38.p7 | 10:27952213 | AAGGACATAATACAA[C/T]GGCTATTTGACATAT | 55130 |
| rs79232773 | snp | C/T | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872921 | TGGTACCATTCCTCC[C/T]GAAACTATTCCAAAC | 55130 |
| rs79270702 | snp | A/G | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27909818 | GTGAGTCTTCATTTG[A/G]AAAAAAAAAAAAAAA | 55130 |
| rs79270712 | snp | A/G | 0.0659589 | 0.169201 | intron-variant | ARMC4 | GRCh38.p7 | 10:27933509 | ACTGAAAAGGGAGGC[A/G]GAGACTAGAGGTGAT | 55130 |
| rs79288310 | snp | C/T | 0.144296 | 0.226554 | intron-variant | ARMC4 | GRCh38.p7 | 10:27880497 | GCTATGGTTTGAATG[C/T]TTATGTCCCCTCAAA | 55130 |
| rs79305827 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | ARMC4 | GRCh38.p7 | 10:27963072 | TAGTGCAGTGGTGCA[A/G]TCTTGGCTCACTGCA | 55130 |
| rs79329127 | in-del | -/A | 0.0659589 | 0.169201 | intron-variant | ARMC4 | GRCh38.p7 | 10:27925655 | AGCCACCACAATGGC[-/A]AAAAAACACTTTAAA | 55130 |
| rs79338047 | snp | A/T | 0.167484 | 0.23599 | intron-variant | ARMC4 | GRCh38.p7 | 10:27931677 | ATACTTGCTTAAAAC[A/T]GTTATATTAATGAGA | 55130 |
| rs79368331 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ARMC4 | GRCh38.p7 | 10:27817851 | CCTTTAGGTATATAT[C/T]CAGTAGGGGGATTGC | 55130 |
| rs79398066 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | ARMC4 | GRCh38.p7 | 10:27913648 | CAAGCAAAAGCTGAA[C/T]AACCCCATTGAAAAG | 55130 |
| rs79407975 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | ARMC4 | GRCh38.p7 | 10:27820161 | CTGCTCCAGGCCCTG[A/C]CTTGTCGCTGGCTGA | 55130 |
| rs79415008 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | ARMC4 | GRCh38.p7 | 10:27883214 | AATGCACACAGAACC[C/T]TTATCACAGGGTGGC | 55130 |
| rs79431376 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ARMC4 | GRCh38.p7 | 10:27839678 | GCTGTGGTTTAAACA[C/T]AAAGTTGGGAGCCAA | 55130 |
| rs79444079 | snp | G/T | 0.110519 | 0.207473 | intron-variant | ARMC4 | GRCh38.p7 | 10:27878162 | AGACAAACAAAAACA[G/T]TCATTGAGAAAGAGA | 55130 |
| rs79470083 | snp | A/G/T | 0.00478085 | 0.0486577 | intron-variant | ARMC4 | GRCh38.p7 | 10:27902275 | CATAGATTCTGGTAC[A/G/T]CTGTGTCATTGTTCT | 55130 |
| rs79489054 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27951731 | TAAGAAACAAAACCT[A/T]TAAGCCATGAAGAAA | 55130 |
| rs79505102 | snp | C/T | 0.0232847 | 0.105357 | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27936627 | ATGTACATCTACAAC[C/T]AACATTAGAATTGAC | 55130 |
| rs79511026 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27923644 | AAACTCTACACTCTG[G/T]TGATAAAGAATCCCA | 55130 |
| rs79521058 | snp | C/T | 0.0592355 | 0.161582 | intron-variant | ARMC4 | GRCh38.p7 | 10:27914789 | CTACAGTATTAGAAA[C/T]GAAGAATTCATTAGA | 55130 |
| rs79582289 | snp | A/C | 0.0345262 | 0.126772 | intron-variant | ARMC4 | GRCh38.p7 | 10:27933273 | AAACTAAACAAAACA[A/C]ATAAGAATGTAACTC | 55130 |
| rs79604949 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27942052 | CAGGTGGGATAGGAA[C/T]GTGGGAAAAATTCTA | 55130 |
| rs79619863 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | ARMC4 | GRCh38.p7 | 10:27829375 | CAGTAATTGCTTTTT[C/T]CAAACTCCCGTTGAC | 55130 |
| rs79627465 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | ARMC4 | GRCh38.p7 | 10:27946561 | CTAGCTGTTTTGAAA[C/T]ACATAATAAATTATT | 55130 |
| rs79650293 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27817998 | TTTTACTGACCTCCT[C/T]GTAGCCCACATCCAC | 55130 |
| rs79657276 | snp | G/T | 0.093417 | 0.194889 | intron-variant | ARMC4 | GRCh38.p7 | 10:27888640 | TCCGTTAATTATTAC[G/T]TTGGCTGTGTAAAAG | 55130 |
| rs79786826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27855130 | TATATGTCAAAATCT[A/G]TCAAAGTGTACACCT | 55130 |
| rs79853268 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | ARMC4 | GRCh38.p7 | 10:27947026 | TCCTCCACATTCATG[A/T]TTAAGTTCAGAATGA | 55130 |
| rs79892424 | snp | C/G | 0.152667 | 0.230274 | intron-variant | ARMC4 | GRCh38.p7 | 10:27820421 | AAACCAATGGACTGT[C/G]AGTGTCAAGCATATG | 55130 |
| rs79925591 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | ARMC4 | GRCh38.p7 | 10:27840389 | TGAGTTGTCACTTTC[A/G]TGCACATCTTTTGGA | 55130 |
| rs79925776 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27876978 | CTTCCAGGACAAAGA[C/G]ACTCAGTCTTCTTGT | 55130 |
| rs79935687 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ARMC4 | GRCh38.p7 | 10:27822869 | CTCTTTCTGTGTGGA[C/T]ATTCCTAAGTTTATC | 55130 |
| rs79954843 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | ARMC4 | GRCh38.p7 | 10:27832467 | CTTGTCCCTTGTATC[A/G]CAGCCAGGTTCTCTA | 55130 |
| rs79958526 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, missense | ARMC4 | GRCh38.p7 | 10:27858205 | ACACCCAGTATGCCA[C/T]ACCCACATTTTTTTC | 55130 |
| rs79986968 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27923186 | GAATGTGAATGCGTT[C/T]AACTCATTAAAACAA | 55130 |
| rs79999233 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27921311 | AACGAAAAAAAAAAA[A/G]AAAAAAAAAAGAACA | 55130 |
| rs80079724 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27921559 | CTTGGAGTTTGCTGG[A/G]ATTCCTGACAACTCA | 55130 |
| rs80093330 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | ARMC4 | GRCh38.p7 | 10:27818225 | TATATCAAAACAAAA[C/T]GTTCCAACTAATTTC | 55130 |
| rs80096294 | snp | A/C | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27893159 | GCCAGACTCCTTCTC[A/C]AAAAAAAAGAAGAAG | 55130 |
| rs80115007 | snp | A/G | 0.0387552 | 0.1337 | downstream-variant-500B, intron-variant | ARMC4 | GRCh38.p7 | 10:27812001 | AAGTCCAGCTGCTTA[A/G]CTCTAAATTCTATTT | 55130 |
| rs80123600 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | ARMC4 | GRCh38.p7 | 10:27866431 | AAAAGCAAAAACAGG[A/G]GCTCTTAGAATTTCA | 55130 |
| rs80161420 | snp | G/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27988351 | GCTTTTTTTTTTTTT[G/T]TTTTGAGACAGAGTA | 55130 |
| rs80168323 | snp | A/G | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27941337 | GGAAAAAAAAAAAAA[A/G]AGCTGGATGTGGTGG | 55130 |
| rs80176158 | snp | A/T | 0.0356815 | 0.128715 | intron-variant | ARMC4 | GRCh38.p7 | 10:27914695 | ATGTGTGTGTATATA[A/T]ATATGTGTGTGTATA | 55130 |
| rs80206258 | snp | A/C | 0.23846 | 0.249734 | intron-variant | ARMC4 | GRCh38.p7 | 10:27898009 | AAAATACTGAAAAAT[A/C]TTTTAAGCCCAATAA | 55130 |
| rs80211932 | snp | C/T | 0.110872 | 0.20771 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983271 | ATCTCTACAAGGATC[C/T]TCTTCCCGAGGTATG | 55130 |
| rs80213855 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | ARMC4 | GRCh38.p7 | 10:27962713 | CCAATATATGCCCTA[C/T]GTCCCTGCAGAGGTC | 55130 |
| rs80223258 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ARMC4 | GRCh38.p7 | 10:27831961 | GGTGCCTGCCTTGAC[C/T]CACAGTGCATCATTG | 55130 |
| rs80241905 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997551 | GCAAAATCGTTATTT[C/T]CGTCAAGATAAATTT | 55130 |
| rs80250565 | snp | C/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27832929 | AGGAATAATTTTTTT[C/T]AAATTATTTTAGTAA | 55130 |
| rs80263991 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | ARMC4 | GRCh38.p7 | 10:27931002 | ACAAAATGACATGTC[C/T]GTATGACTTTTCCCA | 55130 |
| rs80285526 | snp | A/T | 0.00414583 | 0.0453401 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944775 | GAGAGCCCAGGAAGG[A/T]GGGAACAAGACTCCG | 55130 |
| rs80295638 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | ARMC4 | GRCh38.p7 | 10:27889261 | AACTGAGCAAGGGAT[A/G]AGGAAGATTTCACAC | 55130 |
| rs80300626 | snp | C/T | 0.0670745 | 0.170406 | intron-variant | ARMC4 | GRCh38.p7 | 10:27951728 | TCTTAAGAAACAAAA[C/T]CTATAAGCCATGAAG | 55130 |
| rs80301376 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | ARMC4 | GRCh38.p7 | 10:27972216 | TAGAATTTTACTTAA[A/G]GGAGACGTGACAAAT | 55130 |
| rs80311802 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | ARMC4 | GRCh38.p7 | 10:27869167 | AGTGAACTAGAAGGA[A/G]CACAAGAACAAATAA | 55130 |
| rs80319121 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | ARMC4 | GRCh38.p7 | 10:27909339 | AGGAACATTCAATCC[C/T]GGACAAAATTTCACA | 55130 |
| rs80329637 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27902287 | CAGCGTACCAGAATC[C/T]CTGGGACACAGCTAA | 55130 |
| rs80332328 | snp | C/G | 0.167484 | 0.23599 | intron-variant | ARMC4 | GRCh38.p7 | 10:27929115 | TATATTAATCATGTA[C/G]ACTGTACAGAAAAAT | 55130 |
| rs80340487 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27872876 | CTGGCTTCATAAAAT[A/G]AGTTACGGAGGATTC | 55130 |
| rs80344244 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27929294 | ATAGATGAGAGACGA[C/T]TGATAGATAAAATAA | 55130 |
| rs111232762 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | ARMC4 | GRCh38.p7 | 10:27855341 | AGAAATACAAATAAA[A/T]ATTAAAAAGCCAATC | 55130 |
| rs111238983 | snp | A/C | 0.029116 | 0.117091 | intron-variant | ARMC4 | GRCh38.p7 | 10:27864417 | GAGCTTAGAAAAAAA[A/C]AACAGGCTGGAAGTG | 55130 |
| rs111289193 | snp | A/G | 0.420255 | 0.183066 | intron-variant | ARMC4 | GRCh38.p7 | 10:27882173 | ACCTTGTCATAAAAA[A/G]AAAGAAAGAAAGAAA | 55130 |
| rs111293535 | snp | A/G | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27903039 | GATGAACATCGATGC[A/G]AAAATCCTCAATAAA | 55130 |
| rs111329484 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | ARMC4 | GRCh38.p7 | 10:27827121 | TCTTCTCTTGACTTT[A/G]TGAAAATAACACTTT | 55130 |
| rs111329616 | snp | A/C | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27965636 | TGGAGTAGTGTATTC[A/C]TTCTGGCTTCCCATT | 55130 |
| rs111342731 | in-del | -/AC | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27979446 | CACACACACACCCAT[-/AC]ACACACACACACACA | 55130 |
| rs111343859 | snp | A/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27858803 | TGTACACCTTAGTAC[A/T]TTTTTTTTTTTTTTT | 55130 |
| rs111359666 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27830045 | TAGGATAAAATGGAA[C/T]GTCTGAACAGAAAGT | 55130 |
| rs111374625 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27917805 | ATGGTCCTCCCAAAA[A/G]AGAGACTGATGGAGA | 55130 |
| rs111385898 | snp | C/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27852698 | GGGCACAGTGGCTCA[C/T]GCCCATAATCCCAGC | 55130 |
| rs111402649 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ARMC4 | GRCh38.p7 | 10:27911622 | TATGCACTTTCAACT[A/G]TTGCTGTTTCCCAGC | 55130 |
| rs111408365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27971410 | CAGGAAAGGAAGTCT[C/T]GGATGCATTTAACTT | 55130 |
| rs111429965 | snp | C/G/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27961422 | GGGTAATAAGACCTT[C/G/T]CCCTGCACAAACTTA | 55130 |
| rs111433242 | snp | A/C | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27943402 | AGATGGTAGGTACAT[A/C]TTTAAAAACTGGGAT | 55130 |
| rs111440925 | snp | A/G | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27821008 | TGGTTTCAAATTCCT[A/G]ATCTTAAGTGATCTG | 55130 |
| rs111447745 | snp | C/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27974715 | TTTTGCTTAGGATTG[C/T]CTTGGCTATTCTTTT | 55130 |
| rs111488889 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27842009 | TTCCTACCCTATGGC[C/T]GCTGAACAAACACTT | 55130 |
| rs111493203 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27837695 | CGACAAAATAAACTT[C/T]ATAAATATTTCTCTT | 55130 |
| rs111506484 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARMC4 | GRCh38.p7 | 10:27972559 | TAAAGATACAAATAC[A/G]TCAGAAGTGAAAGGC | 55130 |
| rs111516973 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27969256 | AGGAACAGGTCTTCA[A/C]AGGCTGCCACTGTTG | 55130 |
| rs111521735 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ARMC4 | GRCh38.p7 | 10:27986292 | CTGACTACCAAATTG[C/T]CATGTACCATGCAAC | 55130 |
| rs111529425 | snp | A/C | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27881802 | CATTGTGAGATTCAA[A/C]GATAAATAAAACCTT | 55130 |
| rs111585684 | snp | C/T | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27909690 | AGGCTTGGTGGCACG[C/T]GCCTGTAGTCCCAGC | 55130 |
| rs111586634 | snp | A/G | 0.00206122 | 0.0320369 | synonymous-codon, utr-variant-3-prime | ARMC4 | GRCh38.p7 | 10:27936851 | TCCGTGCAGCCTAAC[A/G]AGGTCCCGGGTTTCC | 55130 |
| rs111589311 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ARMC4 | GRCh38.p7 | 10:27831308 | ACATTTTTTCATCAT[C/T]ACCGAAAACGACATT | 55130 |
| rs111635933 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ARMC4 | GRCh38.p7 | 10:27903038 | TGATGAACATCGATG[C/T]GAAAATCCTCAATAA | 55130 |
| rs111644087 | snp | A/T | 0.0225045 | 0.103662 | intron-variant | ARMC4 | GRCh38.p7 | 10:27825410 | GAGAAGAGAAAAGAC[A/T]ACTTAGTGATCTGGG | 55130 |
| rs111645378 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ARMC4 | GRCh38.p7 | 10:27977122 | ATTGGAAAGGTAAAA[C/T]TGAAAAATCTCTAGA | 55130 |
| rs111649256 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27818123 | GCTGCCAGCCTGGAT[A/G]CCAATGGATCCTGAT | 55130 |
| rs111664831 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27960858 | AATACTTCTGGACGT[C/T]GGCTTTACACAAGGC | 55130 |
| rs111675655 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | ARMC4 | GRCh38.p7 | 10:27995211 | AAGAGAAAGAGACAA[C/T]AGCGTCCACCTTTTC | 55130 |
| rs111692906 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | ARMC4 | GRCh38.p7 | 10:27927787 | CTTTACAGAGACTTT[G/T]TCTTCATTCTCCTTA | 55130 |
| rs111699585 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARMC4 | GRCh38.p7 | 10:27835463 | CACTGTGAGGCAGGT[A/G]TGTTCTCTCTCTCTC | 55130 |
| rs111710872 | snp | C/T | 0.0020981 | 0.032321 | intron-variant | ARMC4 | GRCh38.p7 | 10:27907652 | GAGACTGACTTGCAG[C/T]CCGTTCTTACCTTTG | 55130 |
| rs111749440 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27963610 | CCCCCACTGGACTTA[A/G]CTTGTTGCTAAGGCC | 55130 |
| rs111754152 | snp | A/G | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27934666 | CAAGAAGGCTACTAT[A/G]AGAATGTACCTGACA | 55130 |
| rs111769912 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | ARMC4 | GRCh38.p7 | 10:27957613 | GAAGCTGGAAGGTTG[A/G]TGAGTAAAAATGTGA | 55130 |
| rs111803817 | snp | C/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27863557 | AATAATGTGGATCGA[C/T]TTTATATATTCTTTT | 55130 |
| rs111819179 | snp | A/G | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27880875 | GTTGCACCAATACCA[A/G]TTGATTCAGAATGTA | 55130 |
| rs111844406 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27854216 | AAATCAAAAAGACTG[G/T]CCATACCAAGTGTTG | 55130 |
| rs111853627 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | ARMC4 | GRCh38.p7 | 10:27817940 | GACGATTTCTTCTAG[A/T]TACATACTTCGCACC | 55130 |
| rs111856282 | snp | A/T | 0.444444 | 0.157135 | intron-variant | ARMC4 | GRCh38.p7 | 10:27894505 | ATATATGGGGAGCTA[A/T]GCTAAAATTTTTACC | 55130 |
| rs111872011 | snp | A/T | | | utr-variant-3-prime, intron-variant | ARMC4 | GRCh38.p7 | 10:27812189 | AGGCCATATCCTTTT[A/T]ATTAAAATCGCCACA | 55130 |
| rs111883255 | in-del | -/A | 0.0494327 | 0.149241 | intron-variant | ARMC4 | GRCh38.p7 | 10:27864854 | TACTACGCACTTCAC[-/A]TAAGTTATTTCAGTT | 55130 |
| rs111889889 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27841045 | ATTTCAGGTTGATCT[A/G]TTTTAAAAAGAATAA | 55130 |
| rs111896434 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | ARMC4 | GRCh38.p7 | 10:27818858 | TAGATGCCTTATACT[A/G]TTCACTCCTTCCTAG | 55130 |
| rs111954229 | in-del | -/C | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872788 | AATATCCTTGATGAA[-/C]CATTGATGCAAAAAT | 55130 |
| rs111958875 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | ARMC4 | GRCh38.p7 | 10:27930605 | GCACTCCAGCCTAGG[C/T]GACAGAGCCAGACTC | 55130 |
| rs111964038 | snp | A/G | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27833499 | AAATTAAAATAAACA[A/G]TTTAAACTCTGTGGC | 55130 |
| rs111982349 | snp | A/G/T | 0.0116736 | 0.0755028 | missense, synonymous-codon, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27961682 | TTCTGAGGAGCTATC[A/G/T]CTAACAGTTTCCTCA | 55130 |
| rs111989495 | in-del | -/GAA | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27922981 | TGAATGATTAAATAA[-/GAA]GGAGGATGAGGACAC | 55130 |
| rs111989558 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27995820 | CCTATTACCAGAATA[C/T]CTGGACAATCCAAAT | 55130 |
| rs112003468 | snp | A/T | 0.00119737 | 0.0244387 | downstream-variant-500B, intron-variant | ARMC4 | GRCh38.p7 | 10:27812132 | TAACAGAAAGGGAAC[A/T]GTGGAGACGTTCATG | 55130 |
| rs112011675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27831915 | TGCAGTCTGTGAGGG[C/T]ACCAGGACCTACCTG | 55130 |
| rs112019802 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ARMC4 | GRCh38.p7 | 10:27895790 | ATGAGATGCTATTAT[C/T]AAACAGTATAAATGT | 55130 |
| rs112021569 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27903102 | AAAGCTTACCCAACA[C/T]GATCAAGTCAGCTTC | 55130 |
| rs112023424 | snp | C/T | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27919351 | AAAATTGACCTTCCT[C/T]ATATTAAAGGTTTCT | 55130 |
| rs112068569 | snp | A/G | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27824933 | AAGTCTCCAGCCCTG[A/G]CCTGAACTCTAGACT | 55130 |
| rs112075511 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984694 | CACCAGAATGTTTTC[A/G]TGATGTCACCTGCAA | 55130 |
| rs112076215 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27958024 | TTTGCATTTCACAGA[C/T]TTTTAATATCGTTTT | 55130 |
| rs112076285 | snp | C/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27948875 | ACCAGGAGGCATTTC[C/T]TCATTGTCACCATTA | 55130 |
| rs112105379 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27871555 | CAAGGAAGGGATCCA[C/G]TTTCACCTTTCTACA | 55130 |
| rs112132192 | snp | A/G | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27920990 | AGTCTTTCATTACAC[A/G]ATCACATAACACTGG | 55130 |
| rs112139296 | snp | C/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27871976 | CACGATATTGATTCT[C/T]CCTATCCAAGAGCAT | 55130 |
| rs112168386 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27965509 | GATTCATTTGGGCTA[C/T]TGCAGAGCAAGATAC | 55130 |
| rs112168934 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27875900 | ACCAGGAGATTATAT[C/T]GCACGCCTGGCTCGG | 55130 |
| rs112178986 | snp | C/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27932921 | TATAAATCCAGTGGC[C/T]AGCACAAAAGATGCT | 55130 |
| rs112217495 | snp | G/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27987942 | TTTTATTTATAAAAT[G/T]TTTACACCACAGTAA | 55130 |
| rs112218449 | snp | A/G | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27864476 | TGTAACTAAAGCCAT[A/G]CAAATTAGAGAGTGA | 55130 |
| rs112223562 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ARMC4 | GRCh38.p7 | 10:27855683 | GATGGGTGTGTTTGC[A/G]TCTGGGATCATCTTT | 55130 |
| rs112236257 | snp | A/T | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27924878 | GAGAAAGCTATTAAA[A/T]AATTTTTTAAAAAAC | 55130 |
| rs112312796 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872785 | ATCCCTGATGAACAT[C/T]GTTGCAAAAATCTTC | 55130 |
| rs112317008 | snp | A/G | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27834713 | GATTTATGGGTATCT[A/G]CTTGCAGAAAAGGCT | 55130 |
| rs112317402 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27990582 | AAAAAATAAATAGCT[C/T]AGTAACAAAACTTAT | 55130 |
| rs112325030 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27850247 | GTCAGGAGTTTGAGA[C/T]CAGCCTGGCCAACAT | 55130 |
| rs112357969 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | ARMC4 | GRCh38.p7 | 10:27876858 | GCAGAATTGACTAAT[C/T]CTAAAATCTGATGTG | 55130 |
| rs112380719 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ARMC4 | GRCh38.p7 | 10:27923175 | TTCATATCCATGAAT[A/G]TGAATGCGTTTAACT | 55130 |
| rs112386727 | snp | G/T | 0.0279526 | 0.114869 | intron-variant | ARMC4 | GRCh38.p7 | 10:27870821 | AATAAACATACGTGT[G/T]CATGTGTCTTTATAG | 55130 |
| rs112387674 | snp | A/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27995242 | CTTGGAACATTTTTC[A/T]TTCTCAAGACTTTAA | 55130 |
| rs112397106 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | ARMC4 | GRCh38.p7 | 10:27977430 | AAATTAGCCAGGCGC[A/G]GTGGCGGGCGCCTGT | 55130 |
| rs112473879 | snp | C/T | 0.0263992 | 0.111815 | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27996188 | TTTGTATAGCACTTA[C/T]TGATAAAATCTTTCT | 55130 |
| rs112475095 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | ARMC4 | GRCh38.p7 | 10:27833062 | TTCCCCCTTGCCTGG[C/T]CGTGCTTTTTGAAGT | 55130 |
| rs112478252 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27842799 | CTGGCATGAAATCAA[C/T]GGAGTAAAAATAATA | 55130 |
| rs112482000 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27983087 | GTCACCCCAGCAACG[A/G]CCCTTCTTTCCACAC | 55130 |
| rs112482791 | in-del | -/T | 0.17332 | 0.23795 | intron-variant | ARMC4 | GRCh38.p7 | 10:27863819 | CGAGAGAGAAGGTGA[-/T]TTTTTTTTTTTCTAG | 55130 |
| rs112483026 | snp | C/G/T | 0.000148625 | 0.00861929 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27935234 | CACCAAGGTTTCAAT[C/G/T]GCTTTGTATTCCCGA | 55130 |
| rs112483956 | snp | C/G | 0.0170251 | 0.090679 | intron-variant | ARMC4 | GRCh38.p7 | 10:27881873 | TGGGGTGATTTCTTA[C/G]AAATATGAATGCTCA | 55130 |
| rs112486182 | snp | C/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27927859 | CTTCTGTTTTTGTCT[C/T]TCTTTCTTCACTCTG | 55130 |
| rs112525988 | snp | A/T | 0.00204435 | 0.031906 | intron-variant | ARMC4 | GRCh38.p7 | 10:27907825 | GTCATTAGTATGTGA[A/T]GACAAACATTTTAAT | 55130 |
| rs112530212 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27941550 | ATAGCCTGCCTCATG[C/T]GCTACTGAAACCAAC | 55130 |
| rs112531111 | snp | C/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27965255 | GAAGAGTAAGGTAGT[C/T]TGAAGCAATAAAGAG | 55130 |
| rs112533557 | snp | C/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27854328 | TAAAGGTACACATAC[C/T]GTATGATCCAGCCAT | 55130 |
| rs112540359 | snp | A/C | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27848439 | AGATGGATTAAAGAC[A/C]TAAAACCATACAAAC | 55130 |
| rs112548143 | snp | C/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27961401 | AGGATGAATCTTGCA[C/T]CCTCAGGGTAATAAG | 55130 |
| rs112562514 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | ARMC4 | GRCh38.p7 | 10:27961427 | ATAAGACCTTGCCCT[G/T]CACAAACTTAGATAA | 55130 |
| rs112565282 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27839508 | ATTTGGTTTTTAAAC[A/G]GCCCCAAATTGAGGC | 55130 |
| rs112634343 | snp | C/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27856749 | AGGTGGGTGGATCAC[C/T]TGAGGTCAGGAGTTC | 55130 |
| rs112635424 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27964605 | TTTTTGAAGATTTGA[A/T]CTGTTTTCATTTTAG | 55130 |
| rs112640382 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ARMC4 | GRCh38.p7 | 10:27840773 | GCTTTGGAGCTCAGC[A/G]CCTTCTTAGGGCTCT | 55130 |
| rs112657266 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27885522 | CTCAAAAAAAAAAAA[A/T]AAAAAAAAAAAATAT | 55130 |
| rs112662687 | in-del | -/C | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27952551 | CTAATGCTTGCCCAT[-/C]CCCTTTCCCTGACAG | 55130 |
| rs112692014 | snp | C/G | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27890077 | AATCAAAAAAATGGA[C/G]CAAGTACAATGATAG | 55130 |
| rs112723606 | snp | A/G | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27954499 | AATAAACACGAGTGA[A/G]TGAATGAATGAATGA | 55130 |
| rs112726286 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27813850 | TACTGTATTACTTCA[C/G/T]GTAGAGGTGACAGGA | 55130 |
| rs112737906 | snp | C/G | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27865045 | GATCCCATCTCCATA[C/G]CCACCAAATTCTTCC | 55130 |
| rs112744129 | snp | A/G | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27845283 | AACATTCTTAAAGAA[A/G]AGAATTTTCAACCCA | 55130 |
| rs112758334 | snp | C/T | 1.8478e-05 | 0.00303951 | intron-variant | ARMC4 | GRCh38.p7 | 10:27907629 | GTATAGTATTAGAGA[C/T]TCTAGAAGAGACTGA | 55130 |
| rs112792664 | snp | A/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27819595 | AAAAAAAAAAAAAAA[A/T]AAAAAAGTTAACCAG | 55130 |
| rs112798255 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27968804 | TACTAACATTCCTAG[A/T]AACCGTCAGTGTAAA | 55130 |
| rs112841488 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | ARMC4 | GRCh38.p7 | 10:27863073 | TCATCAGTTGATGGA[A/T]ACATAACCTTGTTTT | 55130 |
| rs112850473 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27851842 | TAGCAAAGTCCAAGC[A/C]CAAGAAACATGAAGG | 55130 |
| rs112897095 | snp | C/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27976455 | AAGTGTATATTTATA[C/T]AATAGCAACAAATGA | 55130 |
| rs112899489 | snp | A/G | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27817444 | TTTAATGCACCCACC[A/G]CCCATATAGTGAACA | 55130 |
| rs112900232 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27832956 | GTAAAGTCGAAGGAT[A/G]TATGAGGAAAGCATC | 55130 |
| rs112900658 | in-del | -/A | 0.343254 | 0.231956 | intron-variant | ARMC4 | GRCh38.p7 | 10:27920094 | ATTACCATAAAAGGC[-/A]AAAAAAAAAGAGATA | 55130 |
| rs112909482 | snp | A/T | 0.0399052 | 0.1355 | intron-variant | ARMC4 | GRCh38.p7 | 10:27920299 | TACAAATTAAAAAAA[A/T]TTTAAAGGCTTTTTA | 55130 |
| rs112946333 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | ARMC4 | GRCh38.p7 | 10:27818753 | AGTCCTTGGCCTCCC[C/T]GCTCATAGTTCTGGT | 55130 |
| rs112946470 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27831983 | TGAGTCCAATGTTGT[A/G]CAGGAGCAATGATGC | 55130 |
| rs112954149 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | ARMC4 | GRCh38.p7 | 10:27864543 | GGAGTGAGGTGAGAG[C/T]GGGGAGTGAGGTGAG | 55130 |
| rs112966084 | snp | A/C | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27917313 | CACAAAAAATAGAAA[A/C]TATTTTGAATTAAAT | 55130 |
| rs112969444 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27996030 | ACATTGGCTAAATAG[A/G]AATTAGTCTGTAAAA | 55130 |
| rs113013028 | snp | C/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27988398 | ATTGGAGTGCAGTGG[C/T]GTGATCTCGGGTCAC | 55130 |
| rs113017756 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | ARMC4 | GRCh38.p7 | 10:27910784 | AACAAACAAACAAAC[A/G]AAAAAACAGATACAG | 55130 |
| rs113027857 | snp | A/G | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27911255 | TGTGAGAGCTGGAAC[A/G]AAAAGTCAGAATGTC | 55130 |
| rs113051915 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | ARMC4 | GRCh38.p7 | 10:27930495 | CTCCAGCCTGGGTGA[C/T]AGAGTGAGACCTTGT | 55130 |
| rs113087851 | snp | A/T | | | utr-variant-3-prime, intron-variant | ARMC4 | GRCh38.p7 | 10:27812188 | AAGGCCATATCCTTT[A/T]TATTAAAATCGCCAC | 55130 |
| rs113098144 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | ARMC4 | GRCh38.p7 | 10:27832859 | ATATCATTTTACTGT[C/G]ACCTAAGCAGCTACT | 55130 |
| rs113104262 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARMC4 | GRCh38.p7 | 10:27993426 | AGGCTGAGGCAGGCG[A/G]GTTGCCTGAGCTCAG | 55130 |
| rs113115463 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | ARMC4 | GRCh38.p7 | 10:27880403 | GAGGCAGAAAATGTA[A/G]TTTTCAAGACAGTGG | 55130 |
| rs113120475 | snp | A/G | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27969906 | AGCTCAGGAGTTTGA[A/G]ACTAGCCTGGCCAAC | 55130 |
| rs113120798 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27937354 | CTTTTTTTTTTTTTT[C/T]TGAGAGAGACTCTTG | 55130 |
| rs113122207 | snp | C/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27933863 | CTAAGATTCCAATAA[C/T]CAAATGCAAAAGGAG | 55130 |
| rs113146637 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27935412 | AAATAGTAGAGCTGA[C/T]GTCTAACCCAGCCAT | 55130 |
| rs113150412 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | ARMC4 | GRCh38.p7 | 10:27966231 | TTCAAGCATCTGTTC[C/T]CATTTAATGAGCCAC | 55130 |
| rs113166729 | snp | C/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27819546 | AAGTTCAAGACCATC[C/T]TGGGCAACATAGTGA | 55130 |
| rs113189047 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | ARMC4 | GRCh38.p7 | 10:27978725 | TGAACTCAGGAGGCA[A/G]AGGTTGCAGTGAGCC | 55130 |
| rs113192399 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27951997 | GGAGAATTGCTTGAA[C/T]TGGGGAGGCAGAGGT | 55130 |
| rs113200087 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | ARMC4 | GRCh38.p7 | 10:27875843 | AATCGGGTCACTCCC[A/G]CCCTAATACTGCACT | 55130 |
| rs113207168 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27998498 | AAGGAGAGGCAGGGA[A/G]GCGGCGGGAGAAGTG | 55130 |
| rs113221934 | snp | A/G | 0.021815 | 0.102135 | intron-variant | ARMC4 | GRCh38.p7 | 10:27961557 | AACATACTACCATAG[A/G]CCTTTCTTACCTTTA | 55130 |
| rs113222231 | snp | G/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27882837 | AAGCACCAATCACAA[G/T]CCTTGTCTTTACTTG | 55130 |
| rs113243986 | snp | A/G | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27836305 | ACACAGAGACCAGTG[A/G]TGCTGGGTGACTTGG | 55130 |
| rs113256246 | snp | A/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27961310 | AAATGGCAGCAAGTC[A/T]CAGTGTCAGCTGTTT | 55130 |
| rs113258185 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | ARMC4 | GRCh38.p7 | 10:27942570 | TAAAACATATTTTAT[C/G]TTACATTATCCATTC | 55130 |
| rs113266899 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27870504 | TGCTATCCCTCCCCC[A/C]TCCCCCAACCCCATG | 55130 |
| rs113281170 | snp | A/T | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27995255 | TCATTCTCAAGACTT[A/T]AAACTAGTACTCCCC | 55130 |
| rs113304636 | snp | A/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27969871 | AGCACTTTGGGAGGC[A/T]GAAGTGGGCGGATTA | 55130 |
| rs113308002 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27848602 | CACAGCAAAAGAAAC[G/T]ACCATCAGAGCAAAC | 55130 |
| rs113311195 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27839303 | GCCAGAAGCCATTGC[C/T]TTCATACTTGCTGCC | 55130 |
| rs113336733 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27978089 | TATTTGTAATAGCCC[A/G]AAACCTGAAATAACT | 55130 |
| rs113375418 | in-del | -/A | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27843767 | GCAATACTCTGTCTC[-/A]AAAAAAAACAAAACA | 55130 |
| rs113377194 | snp | A/G | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27861036 | TCACTCTGTTGCCCA[A/G]GCTGAAGTGCAGTGG | 55130 |
| rs113391560 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | ARMC4 | GRCh38.p7 | 10:27955028 | AAAGTTGTCCTATTC[A/G]TTTGTCACTGACTTT | 55130 |
| rs113411123 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | ARMC4 | GRCh38.p7 | 10:27876799 | ACACTTACTGTGTTA[C/T]AACTTATCTCTATAT | 55130 |
| rs113412141 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ARMC4 | GRCh38.p7 | 10:27895081 | TTAATATCAGTTATC[C/T]CCAAGTGCTAAAATT | 55130 |
| rs113417068 | snp | A/G | 0.444444 | 0.157135 | intron-variant | ARMC4 | GRCh38.p7 | 10:27905624 | TCAAACTATACTACA[A/G]GGCTACAGTAACTAA | 55130 |
| rs113449646 | snp | G/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27864897 | AATCATGCAAAATGG[G/T]TATTATTTCCATTTT | 55130 |
| rs113460013 | snp | C/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27934782 | TGGGAAATTGATTAC[C/T]GTGTATTGTAAATCC | 55130 |
| rs113468379 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27919944 | GTGTAAAAATAACCC[A/G]TAATTTAGAACAAAA | 55130 |
| rs113484136 | snp | A/G | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27927428 | CCATGTAAGACTTAA[A/G]GCTCAAAGATGCAGT | 55130 |
| rs113485953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27835041 | AGGCGCAGGGGTTGC[A/G]GCACAGCACATCCGT | 55130 |
| rs113497262 | snp | A/G | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27836404 | TCCTGTCTTTTTTAC[A/G]TCATTAAATAAAAAA | 55130 |
| rs113529757 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27885895 | TTTGGATATATATAT[A/T]TATATATAAAAATAT | 55130 |
| rs113538988 | in-del | -/TTAT | 0.462144 | 0.132269 | intron-variant | ARMC4 | GRCh38.p7 | 10:27893557 | ATCCAAACAAAGACG[-/TTAT]TTATTTCAAAGTGAT | 55130 |
| rs113539167 | snp | A/T | 0.0166325 | 0.0896639 | intron-variant | ARMC4 | GRCh38.p7 | 10:27883357 | ATTAGCCCAAGATAG[A/T]TAATAACAAAATAAA | 55130 |
| rs113541190 | snp | A/C | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27939808 | AGATTCCTGAGTCCC[A/C]TTCTCACAGAAGGAA | 55130 |
| rs113548196 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARMC4 | GRCh38.p7 | 10:27963031 | TTTTTTTTTTTAGAC[A/G]AGATCTCGCTCTGTC | 55130 |
| rs113561552 | snp | C/T | 0.0221135 | 0.1028 | intron-variant | ARMC4 | GRCh38.p7 | 10:27961554 | GCAAACATACTACCA[C/T]AGACCTTTCTTACCT | 55130 |
| rs113570584 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27818598 | AGCTTGATTTCCATA[C/T]GCAAATGAGATTTAG | 55130 |
| rs113583977 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | ARMC4 | GRCh38.p7 | 10:27827998 | GAGTCATCAGAGAGG[A/G]AGGGGAGAACCAGGA | 55130 |
| rs113589832 | snp | A/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27859150 | TCTTCCTTTTTGAAA[A/T]GGGAACGCAGTCATA | 55130 |
| rs113624055 | snp | A/G | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27962758 | ACACTCATCACACCA[A/G]CTTGTCTCCGCCTCC | 55130 |
| rs113640257 | snp | A/G | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27869850 | GACCAAGTCACTTCT[A/G]AGGGAAAGAATAAGA | 55130 |
| rs113640964 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARMC4 | GRCh38.p7 | 10:27975217 | CTCAAAATTTCTTCA[A/G]ACACAAACATGACTA | 55130 |
| rs113642183 | snp | A/G | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27998703 | GGAGCAGGCGAGAGC[A/G]GCAGCGGCGGGGCCA | 55130 |
| rs113664511 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ARMC4 | GRCh38.p7 | 10:27986735 | CATAAGAAACATTTA[C/T]CACACAATTATAGCA | 55130 |
| rs113665563 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ARMC4 | GRCh38.p7 | 10:27910936 | GTTTTCATCAACCAA[C/T]CAATATATAACGTTG | 55130 |
| rs113674006 | snp | A/C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27969318 | TAGGTATGTATCGCC[A/C/G]CCAATTATAGTTTTC | 55130 |
| rs113706952 | in-del | -/A | 0.237882 | 0.249706 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999448 | TACATGTTTCTCTCC[-/A]AAAAAAACAAATATG | 55130 |
| rs113736362 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27891955 | TTAAGAACAAAGAAT[A/T]TAATATATGGACTTT | 55130 |
| rs113786614 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27960503 | AGGCGTGTGCCACCA[C/T]GCCCAGCTAATTTTT | 55130 |
| rs113813980 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27820084 | TCCTGGAGGCCTGGC[C/G]TGGTTAGTTTGGAAG | 55130 |
| rs113819365 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | ARMC4 | GRCh38.p7 | 10:27951847 | TGGGAGGCCAAGGCA[A/G]GTGGATCATCTGAGG | 55130 |
| rs113832406 | snp | A/C/G/T | 3.33557e-05 | 0.00408374 | utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27995152 | ACCCATGGGATCCAC[A/C/G/T]GTGCTCAGACCTGAG | 55130 |
| rs113853496 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | ARMC4 | GRCh38.p7 | 10:27868998 | TTCAATAGGAGCTAA[A/G]GGAAAATAATAAAAG | 55130 |
| rs113858465 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27945003 | GGTTAAGGAACACCG[C/T]ATTCCCATAGAAATG | 55130 |
| rs113860424 | snp | A/C | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27971643 | AATGGCTTGAACCAA[A/C]GATAAAGGGAACATC | 55130 |
| rs113861460 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997784 | AACTAAGATTTTAAA[A/G]TCAAGACCAGTTGCT | 55130 |
| rs113895469 | snp | A/T | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27906506 | CCTGCCAATCCCATT[A/T]TTGGGTATATACCCA | 55130 |
| rs113910577 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27899603 | AGCAGTCCAAAGTCG[A/G]CCTGGCATGCTCAAG | 55130 |
| rs113911654 | snp | C/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27969903 | TTGAGCTCAGGAGTT[C/T]GAGACTAGCCTGGCC | 55130 |
| rs113918983 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | ARMC4 | GRCh38.p7 | 10:27932646 | ACTCCTGTCTGATAT[C/G]TTCATGCAAGCTGCC | 55130 |
| rs113932900 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27819573 | GTGAGACCCTGTCTC[C/T]TAAAAAAAAAAAAAA | 55130 |
| rs113942021 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27906421 | GTTGGTGGGAGTGTA[A/G]ATTAGTTCTACCATT | 55130 |
| rs113951457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872784 | TCCCTGATGAACATC[A/G]TTGCAAAAATCTTCA | 55130 |
| rs113954606 | snp | A/C | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27961432 | ACCTTGCCCTGCACA[A/C]ACTTAGATAAAACAA | 55130 |
| rs113955727 | snp | C/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27943642 | AAATATAAAAATTGG[C/T]CGGGCTTGATGGCGG | 55130 |
| rs113984561 | snp | A/G | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27921825 | GAAGCAAGGCAATAG[A/G]GCAGTATTTTATTTT | 55130 |
| rs114035515 | snp | C/G | 0.0314385 | 0.121371 | intron-variant | ARMC4 | GRCh38.p7 | 10:27988518 | ATTTTTGTATTTTTA[C/G]TAGACAACGGGGTTA | 55130 |
| rs114236526 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | ARMC4 | GRCh38.p7 | 10:27902290 | CGTACCAGAATCTAT[A/G]GGAAATAGCTAAAGC | 55130 |
| rs114247130 | snp | C/T | 0.031825 | 0.122064 | intron-variant | ARMC4 | GRCh38.p7 | 10:27948054 | GACATAAATTCATAA[C/T]GGCCATTTAATTGCA | 55130 |
| rs114271413 | snp | C/T | 0.030665 | 0.119967 | intron-variant | ARMC4 | GRCh38.p7 | 10:27867440 | TGCACAGAAGAGAAA[C/T]TACACGGAATAGCAT | 55130 |
| rs114291159 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | ARMC4 | GRCh38.p7 | 10:27866835 | TCAGCCCCCATGACC[A/C]AAACTCCTCCCATTA | 55130 |
| rs114309925 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | ARMC4 | GRCh38.p7 | 10:27952400 | TTTTATTTTATTTTT[A/T]TTTTTTACCTTAAGT | 55130 |
| rs114430936 | snp | A/T | 0.0322114 | 0.122752 | intron-variant | ARMC4 | GRCh38.p7 | 10:27915933 | TTAGCAGGTGAGCCA[A/T]CAAGGTTGTTTTAAT | 55130 |
| rs114439322 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | ARMC4 | GRCh38.p7 | 10:27917617 | AAAAATGGTAAACCA[A/C]TAAAGAAAGGTTGAC | 55130 |
| rs114510803 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ARMC4 | GRCh38.p7 | 10:27852683 | AAGCTAACCGTGGCC[A/G]GGCACAGTGGCTCAC | 55130 |
| rs114515937 | snp | A/G | 0.00437018 | 0.0465402 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940043 | ATTTATGTGTTCAAG[A/G]CGTGAATATAAGTAA | 55130 |
| rs114530399 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | ARMC4 | GRCh38.p7 | 10:27892279 | TAAATGGTAAATGTT[C/T]AAATAAAACTTCTTT | 55130 |
| rs114544549 | snp | A/G/T | 0.0327046 | 0.12426 | intron-variant | ARMC4 | GRCh38.p7 | 10:27913354 | GTACTCAGTGTTTGC[A/G/T]TCCCACTGATAAGTG | 55130 |
| rs114552413 | snp | G/T | 0.021333 | 0.101051 | intron-variant | ARMC4 | GRCh38.p7 | 10:27913182 | AGGTTTGTTAAATAG[G/T]TAAATTACGTGTCGC | 55130 |
| rs114555589 | snp | C/T | 0.0659589 | 0.169201 | intron-variant | ARMC4 | GRCh38.p7 | 10:27858985 | CTTTTTGAGCTTAAA[C/T]TAACTGACAATTGTC | 55130 |
| rs114557590 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | ARMC4 | GRCh38.p7 | 10:27829809 | GAGTTTTAGAACAGA[A/G]TAATACTTCTTCCTC | 55130 |
| rs114567733 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | ARMC4 | GRCh38.p7 | 10:27909208 | CCTGCCCTATCTTCT[C/T]GAAAATTTCGCAGCA | 55130 |
| rs114586706 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | ARMC4 | GRCh38.p7 | 10:27963854 | GGACAACAGACTGTG[A/G]GTTAAATGTCTCATT | 55130 |
| rs114598725 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | ARMC4 | GRCh38.p7 | 10:27970321 | TGAGACTCTAGCCTT[C/T]TCATGGTATTAAAGT | 55130 |
| rs114652892 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27915586 | GTATATATAGCACAG[G/T]AGGTATGGGGAATTA | 55130 |
| rs114654636 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27821213 | ATTTTCTGTGTGCTC[C/T]GGGTATGAATATTTG | 55130 |
| rs114679679 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | ARMC4 | GRCh38.p7 | 10:27966345 | GAATAAGCCTAAGTT[A/C]TTTGAGGAAAGCCTA | 55130 |
| rs114682555 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | ARMC4 | GRCh38.p7 | 10:27897814 | CAGGGAGTATTCAGA[C/G]GGTAGGTGAAGTTCA | 55130 |
| rs114695749 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27981946 | TTAGTTGATGATGTC[A/G]TAAAAGTCTTCAAGG | 55130 |
| rs114715337 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27855607 | TTAGTATCTAAAATC[C/T]GTTTACTTGACTCAC | 55130 |
| rs114716953 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | ARMC4 | GRCh38.p7 | 10:27827950 | AAAGTTCTAGCAAGC[A/G]GATTGGCCAGAAGGA | 55130 |
| rs114719046 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27965794 | TTTACAAAAATTGAA[A/T]TAGTGGAATCATGAT | 55130 |
| rs114786512 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27877844 | TTTGCAATTTATAAA[C/G]GACTTCCACATGCAT | 55130 |
| rs114787195 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | ARMC4 | GRCh38.p7 | 10:27877720 | CTTAAAAACCTAGTC[A/G]TTGCCAGTTTCACCA | 55130 |
| rs114807568 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ARMC4 | GRCh38.p7 | 10:27854373 | TTACCTAAGAGAAGA[A/G]GAAGCAAATGTCCAC | 55130 |
| rs114809104 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | ARMC4 | GRCh38.p7 | 10:27836244 | TATTTCATCTTTCCT[A/G]TAACTCTTTGAGGAA | 55130 |
| rs114809817 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27878821 | TATCACAATAAGATC[C/T]TTGTTCTGTTCCCAG | 55130 |
| rs114819736 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27981244 | CTTGGAAATTGACAA[C/T]AGTGATATTTGTACA | 55130 |
| rs114851806 | snp | A/G | 0.0547245 | 0.156101 | intron-variant | ARMC4 | GRCh38.p7 | 10:27855458 | TAGTAAACTCTTCTC[A/G]GCACTCCAAGGAATG | 55130 |
| rs114862833 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ARMC4 | GRCh38.p7 | 10:27817371 | TTTTGGATATATTTC[A/G]AGGGTACAAGTGCAA | 55130 |
| rs114901771 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27887520 | ACCTAACAACAGCAG[A/G]ATACTCATTTTTCTC | 55130 |
| rs114915457 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | ARMC4 | GRCh38.p7 | 10:27945513 | ATGGGATGGGCAGGA[C/T]GAAGAAGAAAGCAAG | 55130 |
| rs114916912 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant | ARMC4 | GRCh38.p7 | 10:27918178 | AACTTGTCCTATAGG[G/T]CCTGCATAAACCTGA | 55130 |
| rs114922970 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | ARMC4 | GRCh38.p7 | 10:27934090 | TAAAAAGAAGTTTCC[C/T]TGCACAAGCTCTCTT | 55130 |
| rs114934454 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | ARMC4 | GRCh38.p7 | 10:27851260 | AATTATCCCTACTCT[A/G]GTCTTGCTAACAAAG | 55130 |
| rs114990538 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | ARMC4 | GRCh38.p7 | 10:27934785 | GAAATTGATTACCGT[A/G]TATTGTAAATCCTCC | 55130 |
| rs115082402 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27941499 | CCCGAACCAAAAAAA[A/G]GAAAAAAAAAAAACC | 55130 |
| rs115088009 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | ARMC4 | GRCh38.p7 | 10:27988430 | GCAACCTCTGCCTCC[A/G]GAGCTCAAGCAATCC | 55130 |
| rs115092513 | snp | A/G | 0.0788843 | 0.182262 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27959611 | GCCTGAATCTAGCCC[A/G]TGCTCCATGCTAGTG | 55130 |
| rs115105495 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ARMC4 | GRCh38.p7 | 10:27931959 | TAATATACCTAACCT[A/G]CTGAACATCATAGCT | 55130 |
| rs115131168 | snp | C/T | 0.031825 | 0.122064 | intron-variant | ARMC4 | GRCh38.p7 | 10:27863753 | CAAAAAGTTATCCAG[C/T]GTGAAAGGGATTCTG | 55130 |
| rs115201161 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ARMC4 | GRCh38.p7 | 10:27876325 | GACACCCCACACTGC[C/T]GGGTACCCCTCTGAG | 55130 |
| rs115203077 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ARMC4 | GRCh38.p7 | 10:27914316 | TCCATTTTAAAGATG[C/T]CATTTTTTCTTTTCA | 55130 |
| rs115224051 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | ARMC4 | GRCh38.p7 | 10:27957817 | AGTTCATTGACCTGT[C/T]TGGGTATTAATGAGC | 55130 |
| rs115227486 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ARMC4 | GRCh38.p7 | 10:27831170 | CTTACCTCTGCAGAT[A/G]ATGCTACCTCGGCCT | 55130 |
| rs115231699 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ARMC4 | GRCh38.p7 | 10:27833329 | GCAATAGTCGTACTT[C/T]GCAATGATTGCCTGT | 55130 |
| rs115264203 | snp | A/C | 0.0252325 | 0.109451 | intron-variant | ARMC4 | GRCh38.p7 | 10:27980553 | GATATACAGATAACC[A/C]ACAAATATATGAAAA | 55130 |
| rs115283120 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | ARMC4 | GRCh38.p7 | 10:27836663 | TTCTTACCTTTATGG[C/T]TGACTCTCAAATCAT | 55130 |
| rs115379761 | snp | A/C/G | 0.0236746 | 0.106192 | intron-variant | ARMC4 | GRCh38.p7 | 10:27820483 | GTGTGTTGGCTATTC[A/C/G]CGGAGTCAACCAGAT | 55130 |
| rs115436737 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | ARMC4 | GRCh38.p7 | 10:27863281 | CACATCTGGGGGCCA[C/T]TGTGAACAGTGAAAT | 55130 |
| rs115476225 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | ARMC4 | GRCh38.p7 | 10:27859346 | TTTATAATGGAAAGG[C/T]TGACACATTCAAACA | 55130 |
| rs115503923 | snp | C/G | 0.0217236 | 0.101931 | intron-variant | ARMC4 | GRCh38.p7 | 10:27835045 | GCAGGGGTTGCGGCA[C/G]AGCACATCCGTACTT | 55130 |
| rs115527235 | snp | C/T | 0.0655868 | 0.168795 | intron-variant | ARMC4 | GRCh38.p7 | 10:27952838 | GTAAATTGATATTTG[C/T]TTTCTGTAAGGAGCT | 55130 |
| rs115558664 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ARMC4 | GRCh38.p7 | 10:27826811 | TTAAACATATCTGCT[A/G]TCTCAGAACAGAAAC | 55130 |
| rs115562452 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | ARMC4 | GRCh38.p7 | 10:27840691 | AGGAAGCCAACTGGC[A/T]TAGAAAGAATAAAAG | 55130 |
| rs115716475 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | ARMC4 | GRCh38.p7 | 10:27954829 | AAAACACGACAAATT[C/T]TTTTGTGGGCAATAT | 55130 |
| rs115727002 | snp | A/C/G | 0.00993419 | 0.0697739 | intron-variant | ARMC4 | GRCh38.p7 | 10:27930535 | ACAAAAACAGGCTGA[A/C/G]AGAATGGCGTGAACC | 55130 |
| rs115728220 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | ARMC4 | GRCh38.p7 | 10:27869968 | ATCAGTGTTCTAATA[C/T]TGAGTCAAAATGACC | 55130 |
| rs115792428 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27858968 | GCCTATACATTTTTA[A/C]ACTTTTTGAGCTTAA | 55130 |
| rs115826944 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ARMC4 | GRCh38.p7 | 10:27824641 | TTAAATTATCTAGAA[C/T]GATCCATAGATCTCT | 55130 |
| rs115867006 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27994294 | TCACCCCTCCCCGCC[A/G]CCTCCTGCTTCTAGC | 55130 |
| rs115909624 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | ARMC4 | GRCh38.p7 | 10:27829048 | TATAGAATTCATCCC[C/T]CATGTGGATAAAATT | 55130 |
| rs115922911 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | ARMC4 | GRCh38.p7 | 10:27962365 | TGGCCCACGTGCCTC[A/G]TGGTTACCACACTGG | 55130 |
| rs115923885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983500 | ATGCAAGCTGCAGTT[A/G]TGACATCTGTATTAT | 55130 |
| rs115977942 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27919330 | TGAACCTTAAAGGAC[A/G]ACCGAAAAATTGACC | 55130 |
| rs115985592 | snp | A/C | 0.0205511 | 0.0992634 | intron-variant | ARMC4 | GRCh38.p7 | 10:27887218 | CAAGATTGTCCATAC[A/C]AATAACAGACAAAAT | 55130 |
| rs116149695 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27941500 | CCGAACCAAAAAAAA[A/G]AAAAAAAAAAAACCA | 55130 |
| rs116265005 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | ARMC4 | GRCh38.p7 | 10:27834034 | GTGCTGGCCAGAAGG[G/T]GAGTGACATCCAGGC | 55130 |
| rs116272781 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | ARMC4 | GRCh38.p7 | 10:27834457 | GTGATAACCTAATCA[C/T]CACACGGCCACACCA | 55130 |
| rs116340948 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | ARMC4 | GRCh38.p7 | 10:27910376 | CAATTCCAGAGCTCG[A/G]TATTTAAATTTTTTA | 55130 |
| rs116361961 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ARMC4 | GRCh38.p7 | 10:27831470 | CAAAGTGCCTTATAA[A/G]ATACTGATTCATTTG | 55130 |
| rs116437165 | snp | A/T | 0.0225045 | 0.103662 | intron-variant | ARMC4 | GRCh38.p7 | 10:27914544 | GCTTTTCTTTCATTA[A/T]CTAGAGCTCAATTAC | 55130 |
| rs116446960 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | ARMC4 | GRCh38.p7 | 10:27841728 | CTGATCCTGTCCCTA[C/T]ACACCTCCAAGAGTG | 55130 |
| rs116482995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27921170 | AGAAATACCTGTTCC[C/T]TAATTTCCTTGATCT | 55130 |
| rs116484491 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | ARMC4 | GRCh38.p7 | 10:27831015 | AGCTGAGATGTGATG[C/T]TAAAGGCACCATGAG | 55130 |
| rs116485790 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | ARMC4 | GRCh38.p7 | 10:27951717 | ACCTTCCTAGTTCTT[A/G]AGAAACAAAACCTAT | 55130 |
| rs116546071 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | ARMC4 | GRCh38.p7 | 10:27895389 | ACTGCAGCCTCCTGG[C/G]TTCAAATGATTCTTG | 55130 |
| rs116550256 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | ARMC4 | GRCh38.p7 | 10:27933081 | GGCAACATGGCAAGA[A/C]CCCCAACTCCACAAA | 55130 |
| rs116574877 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | ARMC4 | GRCh38.p7 | 10:27977227 | TTGGACTGTTTCAAA[A/G]TTGAAGACTCTTGCT | 55130 |
| rs116639706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27854493 | GGGCACAGTGGCTTA[C/T]GCTTGTAATCCCAAC | 55130 |
| rs116644611 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | ARMC4 | GRCh38.p7 | 10:27941837 | AAGGTCAACTTCCAC[A/T]GATACTGCCCGTAAC | 55130 |
| rs116673087 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ARMC4 | GRCh38.p7 | 10:27817299 | TTCAGAATTTTTATT[A/G]ATCTCTTTGTTTATA | 55130 |
| rs116702524 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27876785 | GCACACTTTCCAGTA[C/T]ACTTACTGTGTTACA | 55130 |
| rs116739820 | snp | A/G | 0.00354865 | 0.041973 | intron-variant | ARMC4 | GRCh38.p7 | 10:27994882 | AATACTATGTACAAC[A/G]AAGATATCAAATCCT | 55130 |
| rs116794667 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ARMC4 | GRCh38.p7 | 10:27818129 | AGCCTGGATGCCAAT[A/G]GATCCTGATATTCAT | 55130 |
| rs116796994 | snp | A/T | 0.0659589 | 0.169201 | intron-variant | ARMC4 | GRCh38.p7 | 10:27924986 | TCCAGAGTATTTAAA[A/T]TGAAAAAAAAAAAAA | 55130 |
| rs116800333 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | ARMC4 | GRCh38.p7 | 10:27958041 | TTTAATATCGTTTTG[G/T]GTCTCCATATAAAAT | 55130 |
| rs116824753 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ARMC4 | GRCh38.p7 | 10:27908196 | ATTGACTTACCTTAC[C/T]GTATGACATATTTTA | 55130 |
| rs116825463 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | ARMC4 | GRCh38.p7 | 10:27861739 | CCTGTAATGGGCATA[C/T]TATTACTGAATCGGA | 55130 |
| rs116828316 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | ARMC4 | GRCh38.p7 | 10:27949110 | AACATTTGCTAAGTT[G/T]AAATGAGCAATGTAT | 55130 |
| rs116858785 | snp | C/T | 0.143959 | 0.226396 | intron-variant | ARMC4 | GRCh38.p7 | 10:27846898 | GAATCCCTCAATAGA[C/T]CAATTGTTGCTCTGA | 55130 |
| rs116922701 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | ARMC4 | GRCh38.p7 | 10:27915099 | AAGAAGCTCAGCGAA[A/C]CCTAAATAAAAGTAA | 55130 |
| rs116955013 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | ARMC4 | GRCh38.p7 | 10:27924197 | GATCAAAATGTAGTA[C/T]GAGAAATATCTAACA | 55130 |
| rs116964508 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27842579 | AATTTATTAAACAGA[A/G]AATTCAAAAACATAT | 55130 |
| rs117100960 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27884056 | CAAATTTGATGAGAA[A/T]CTTTACATATGCAAG | 55130 |
| rs117111360 | snp | A/G | 0.138546 | 0.223781 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27960859 | ATACTTCTGGACGTC[A/G]GCTTTACACAAGGCC | 55130 |
| rs117119035 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27964601 | TTTGTTTTTGAAGAT[A/C/T]TGATCTGTTTTCATT | 55130 |
| rs117126496 | snp | A/C | 0.0926964 | 0.194308 | intron-variant | ARMC4 | GRCh38.p7 | 10:27993938 | AGAATGCCTAAGGTG[A/C]AAAATAAACTGAGGC | 55130 |
| rs117131389 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ARMC4 | GRCh38.p7 | 10:27828342 | GGAAAGGAAGATTAA[A/G]GCTAAATATGCAGAA | 55130 |
| rs117144428 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARMC4 | GRCh38.p7 | 10:27820039 | ATGGTGATTCTTTTG[C/T]CAGTTCAGAAGTCTG | 55130 |
| rs117162925 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | ARMC4 | GRCh38.p7 | 10:27985676 | ATAGCATGCTTTCCT[A/G]AGCCTACAGACCCAG | 55130 |
| rs117212827 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | ARMC4 | GRCh38.p7 | 10:27987747 | ACCAGCAAGCCTAGT[A/G]ACCAATAGGATATAA | 55130 |
| rs117320029 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | ARMC4 | GRCh38.p7 | 10:27932184 | CCAGCAATCCTTCTG[A/C]CTCTGCCTCCCAAAG | 55130 |
| rs117369964 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ARMC4 | GRCh38.p7 | 10:27869240 | AGGGTAATGTAAAAA[C/T]AGTTAACAAAAAATT | 55130 |
| rs117370159 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ARMC4 | GRCh38.p7 | 10:27951013 | AAAAGTTCCCATGTC[A/G]GGATTAGCAAAATAA | 55130 |
| rs117373849 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ARMC4 | GRCh38.p7 | 10:27844962 | TCTATTAGCTCAGCC[C/T]CTTCTAGGCACATTC | 55130 |
| rs117377832 | snp | A/G | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983279 | AAGGATCCTCTTCCC[A/G]AGGTATGAGCATTAA | 55130 |
| rs117450279 | snp | C/T | 0.0170251 | 0.090679 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999155 | TATTCAACTTTGCAT[C/T]TCCCTTTCTCAAACA | 55130 |
| rs117515566 | snp | G/T | 0.000560658 | 0.0167336 | missense | ARMC4 | GRCh38.p7 | 10:27935199 | ACAAGTACTTCTTCA[G/T]GCTGATCTGTTAGAA | 55130 |
| rs117525151 | snp | C/G | 0.16846 | 0.236329 | intron-variant | ARMC4 | GRCh38.p7 | 10:27952455 | CAGGTTTGTTACATA[C/G]GTAAACGTGTGCCAT | 55130 |
| rs117603735 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ARMC4 | GRCh38.p7 | 10:27888309 | TCCCTTTTCTCCTCA[C/T]CCTTGCCAACATACA | 55130 |
| rs117636204 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | ARMC4 | GRCh38.p7 | 10:27922024 | CTACAAAAATTAGCC[A/G]GGCATGGTGGGATGT | 55130 |
| rs117708970 | snp | A/G | 0.138546 | 0.223781 | intron-variant | ARMC4 | GRCh38.p7 | 10:27880777 | CCAGCCTCCAGAATT[A/G]TAAGACATAAATTTC | 55130 |
| rs117723546 | snp | A/G | 0.00748068 | 0.0606991 | synonymous-codon, intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27971233 | AGAAATGTCTTTGCG[A/G]AGGGCAGCTGCTTCT | 55130 |
| rs117806824 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27928547 | TCTATTGCCTGTTCA[C/G]TTATCTATGACATGC | 55130 |
| rs117833790 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | ARMC4 | GRCh38.p7 | 10:27892502 | GATAATGAATGGACC[A/G]ATAATTTTTAAGCTG | 55130 |
| rs117840923 | snp | C/G | 0.143284 | 0.226079 | intron-variant | ARMC4 | GRCh38.p7 | 10:27843611 | CCTATACTAAAAATA[C/G]AAAAAAATTAGCTGG | 55130 |
| rs117849570 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27980217 | AAACTATACAATCCT[C/T]AGAGGAAAAACACAG | 55130 |
| rs117851143 | snp | C/G | 0.0154538 | 0.0865337 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:28000000 | CGATCTCGGCTCACC[C/G]CAACCTCTGCCTCCC | 55130 |
| rs117867611 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | ARMC4 | GRCh38.p7 | 10:27831131 | TGCTCCCAGAAGTCC[A/G]TCTGCCTTGTGCTTG | 55130 |
| rs117895105 | snp | A/G | 0.167158 | 0.235875 | intron-variant | ARMC4 | GRCh38.p7 | 10:27938039 | ACCTCTACCTCGTGG[A/G]TTCAAGCAATTCTCG | 55130 |
| rs117907867 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ARMC4 | GRCh38.p7 | 10:27956800 | TTTTCATTATAATGT[A/G]TATAAAATGCAAATC | 55130 |
| rs117915541 | snp | C/T | 0.109814 | 0.206997 | intron-variant | ARMC4 | GRCh38.p7 | 10:27974578 | CTCTATTCTGTTTCA[C/T]TGGTCTATGTGTCTT | 55130 |
| rs117946130 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27850495 | GTGGGAGGCGGAGGT[A/T]GTAGTGAGCTGATAT | 55130 |
| rs117980135 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27948004 | CAACTTCCACATCTT[G/T]TGAGCTTTATTTCAT | 55130 |
| rs117992370 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27982817 | GCTAAGCTCCTTCTA[A/G]CTGGTTCTGTGAATA | 55130 |
| rs118046108 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27958007 | ACCTAGAGACATTCA[A/G]TTTTGCATTTCACAG | 55130 |
| rs118085243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27954584 | TGTCATGTTTCAGTC[A/G]TTAAGTTGATGTGGT | 55130 |
| rs118092192 | snp | C/T | 0.0926964 | 0.194308 | intron-variant | ARMC4 | GRCh38.p7 | 10:27973748 | GCTGCAATGAACATA[C/T]GTGTGCATGTGTCTT | 55130 |
| rs118095999 | snp | A/T | 0.0322114 | 0.122752 | intron-variant | ARMC4 | GRCh38.p7 | 10:27862141 | TGGCGGTGAAGATGA[A/T]AGTTAACACTTACAT | 55130 |
| rs118124503 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27982648 | AGGCTCCAGCATTTT[G/T]GTACCAACCCAAGCC | 55130 |
| rs118139752 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | ARMC4 | GRCh38.p7 | 10:27949546 | CAGTATATGCAAAAA[C/T]GCAGGGGAGTAGAGC | 55130 |
| rs118166584 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27836095 | CTCAGGGGTGGCAGA[G/T]TCAGAAGGAAATCTG | 55130 |
| rs137866505 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ARMC4 | GRCh38.p7 | 10:27819724 | GTGAGCTATGATTGC[A/G]CCATTGCTGTGACCT | 55130 |
| rs137868735 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | ARMC4 | GRCh38.p7 | 10:27928912 | ACTATCCCCATTTTA[G/T]GTATATGGTGACCAA | 55130 |
| rs137868851 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27894286 | AGTGGGGAAAGTTTT[A/G]GATAGTGATATAAAT | 55130 |
| rs137875876 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997406 | ACATTTGTTTTGGTA[A/G]TCTTATAAAGATTGC | 55130 |
| rs137880836 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27955129 | GGTACTCATTTGCCT[G/T]TCTAACTACTGGAGT | 55130 |
| rs137900360 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARMC4 | GRCh38.p7 | 10:27896468 | ATAGATGGATGATTG[A/G]TTGAAAGATAGAGAG | 55130 |
| rs137901082 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | ARMC4 | GRCh38.p7 | 10:27823441 | ACAGTCTGAATTTGA[A/C]TCCTGACTTCACATC | 55130 |
| rs137936133 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27849604 | GGCAAAAGCATTGCC[A/T]AGAGCTCCCCATGGA | 55130 |
| rs137949016 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27915267 | TAACAGAATGCCATA[C/T]GCTGGGTGGCTTGTA | 55130 |
| rs137973827 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | ARMC4 | GRCh38.p7 | 10:27841648 | TGATCTGCCTGCCTC[A/G]GCCTCCCAAACTGCT | 55130 |
| rs138030968 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ARMC4 | GRCh38.p7 | 10:27988498 | CATGCCACCATGCCT[C/T]GCTAATTTTTGTATT | 55130 |
| rs138088474 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | ARMC4 | GRCh38.p7 | 10:27868329 | AATCCCATTACTTGG[A/G]TATATACCCAAAGGA | 55130 |
| rs138090734 | snp | C/T | 0.029116 | 0.117091 | intron-variant | ARMC4 | GRCh38.p7 | 10:27901778 | TGACCTAAATATATA[C/T]GCACCCAGTACAGGA | 55130 |
| rs138094361 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ARMC4 | GRCh38.p7 | 10:27934057 | ATAGTGAGTAAGTCT[C/T]ATGAGATCTGATAGT | 55130 |
| rs138135485 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27925194 | ATGACTAAGTGAGAC[A/T]TATTCCAGGAATGCA | 55130 |
| rs138140902 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | ARMC4 | GRCh38.p7 | 10:27994205 | CTCAGATTTGAAAGG[A/C]TCTAATCTGAGGACA | 55130 |
| rs138144984 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27828261 | GAGAGAATGCTACTT[C/T]CCTGATATGATGATT | 55130 |
| rs138174899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27942579 | TTTTATGTTACATTA[C/T]CCATTCTTATAATTT | 55130 |
| rs138191635 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27976684 | TCCTAAATTCGTCTA[C/T]AAATTCAAGGCAATC | 55130 |
| rs138192807 | snp | C/T | | | synonymous-codon, utr-variant-5-prime, intron-variant | ARMC4 | GRCh38.p7 | 10:27981547 | AATTGAACCTTTTCT[C/T]TCATAATTAACGTCC | 55130 |
| rs138203110 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27832118 | GTTCAGATGCTTGGC[A/G]TATTTCAGCTGCAGC | 55130 |
| rs138205369 | snp | G/T | 0.000841535 | 0.0204954 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27944311 | CGGCTGCCAAACATT[G/T]TAGACTCTTGTGTGG | 55130 |
| rs138207271 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27836976 | GCTTTGCAGGGAATG[A/T]CGCTTAAGTCAGGCT | 55130 |
| rs138218825 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | ARMC4 | GRCh38.p7 | 10:27904574 | AATTCCCATTTGTAC[A/T]TAGGTCTATTCTGTA | 55130 |
| rs138219785 | snp | C/T | 0.00408 | 0.0449817 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27935171 | GCATTCTCCCAAGGC[C/T]CCAACCACATTCACA | 55130 |
| rs138232654 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997633 | GAACCGTAGCAATGC[A/C]CAAGTTTTATTCAAG | 55130 |
| rs138252726 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27876469 | GCAAACTCCAGCAGA[A/C]CTGCAGCTGAGGGTC | 55130 |
| rs138253799 | in-del | -/GGAAAG | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27924043 | AAGAGAAAGAAAGAA[-/GGAAAG]AGAAAGAAAGAAAGA | 55130 |
| rs138291121 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27853606 | TTATAATAATACAGA[A/T]TACAGGCATGAGCCA | 55130 |
| rs138298252 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27946684 | TCATCCCTTCATACC[A/C]TGTCTTATATATAAT | 55130 |
| rs138323842 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27843449 | TCTACATATTCCTGA[C/T]TACCTGAGAGGTAAC | 55130 |
| rs138350628 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | ARMC4 | GRCh38.p7 | 10:27966001 | TCCCAGTGGGTTCTC[A/G]TCCATAAAAGTCTTT | 55130 |
| rs138356597 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | ARMC4 | GRCh38.p7 | 10:27827032 | TGCATCCAGGGGACA[C/T]TTTTGGTTCTTGTCT | 55130 |
| rs138372376 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | ARMC4 | GRCh38.p7 | 10:27823073 | CTTGATGACTGGCTG[A/G]GTCAGGGAATTGTGG | 55130 |
| rs138372794 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27989320 | TTCAGATAGGAACTG[C/T]ACATAGAAGACATTT | 55130 |
| rs138406839 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27969168 | CCTCATTCTGACACT[C/T]GGAGCTGTCTCTTTC | 55130 |
| rs138412277 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | ARMC4 | GRCh38.p7 | 10:27888387 | TAAGATGATATCTCA[C/T]TGTGGTTTTTATTTG | 55130 |
| rs138420702 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27863029 | GAAACATAGGACTAG[G/T]TTCCTGCAAGCCTCT | 55130 |
| rs138425193 | snp | A/T | 0.00138561 | 0.0262847 | missense, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984283 | TCATGGGACTTAAAC[A/T]TATTTCTCTGAAATA | 55130 |
| rs138486026 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ARMC4 | GRCh38.p7 | 10:27908429 | GCCATCTCTCCACCA[C/T]CTGTCTTCTGTTTAT | 55130 |
| rs138486505 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ARMC4 | GRCh38.p7 | 10:27971679 | GGTAGACAGGTATGA[C/T]ATATTACAGAGGAAT | 55130 |
| rs138500328 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27881613 | TTGCACTCCAACCTG[A/G]GCAACAGAGCAAAAT | 55130 |
| rs138500496 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | ARMC4 | GRCh38.p7 | 10:27812317 | ATGTCATATCTCGAA[A/G]ACATTAAATAGAAAC | 55130 |
| rs138508233 | snp | A/G | 0.000153988 | 0.00877327 | missense, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27961671 | TCTTCCTCACTTTCT[A/G]AGGAGCTATCGCTAA | 55130 |
| rs138517767 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27920436 | TATGCGTGCATATCA[C/T]AACTGGCTGGATGAG | 55130 |
| rs138524560 | snp | A/G | 0.110519 | 0.207473 | intron-variant | ARMC4 | GRCh38.p7 | 10:27875481 | TTTCCCCATCTTTGT[A/G]GTTTTATCTACCTTT | 55130 |
| rs138537207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27886324 | ATATACATATCAGTA[A/G]ATTTCTCCAGAGAAG | 55130 |
| rs138537587 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27815722 | TGTTAGAGTTCATCA[A/G]AACAAATTCCCCTTC | 55130 |
| rs138546479 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27858319 | TAGGAAGAAGAGGTC[A/G]AGAGAGACAATCTCC | 55130 |
| rs138548475 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | ARMC4 | GRCh38.p7 | 10:27924180 | AAAAGTCAACACACT[C/G]TGATCAAAATGTAGT | 55130 |
| rs138584224 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27995509 | AAAAAAAAGGAAGTG[G/T]AAGAGGTTTATATTA | 55130 |
| rs138588942 | snp | A/G | 0.000692019 | 0.0185884 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27812561 | AGCCTGCGGATATTG[A/G]ATATACAACCAGCTG | 55130 |
| rs138645104 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27933458 | ATTATCAGATATGCA[A/G]TTTAGGAAAGTAAAT | 55130 |
| rs138678037 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27882177 | TGTCATAAAAAAAAA[A/G]AAAGAAAGAAAGAAA | 55130 |
| rs138692404 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ARMC4 | GRCh38.p7 | 10:27951280 | AACTCATTCTAAAGA[C/T]GATCTAGAATGAAAA | 55130 |
| rs138732974 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARMC4 | GRCh38.p7 | 10:27912352 | AATCAAACTGCCTGG[C/T]TGGCAAAATAACAGC | 55130 |
| rs138768992 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARMC4 | GRCh38.p7 | 10:27958279 | CTGGGACAGAAATAG[C/T]GCATCTCTTTTTGGC | 55130 |
| rs138798150 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27837638 | GCTTTTCTAATTCCC[A/T]CTCTCTGCCAGGATT | 55130 |
| rs138799259 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27902523 | AGCTGGTTTTTTGAA[A/G]ACATTAACAAAATAA | 55130 |
| rs138802068 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27946329 | CCCTCCTCCATAGCA[A/C]GAGCTTGTGCATTTG | 55130 |
| rs138806453 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27965407 | AAGCTTTGGTGCATA[A/G]GGTGAGGATATAAGA | 55130 |
| rs138811545 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872721 | CCACTTGATCATAGT[G/T]GATAAGCTTTTTGAT | 55130 |
| rs138815698 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | ARMC4 | GRCh38.p7 | 10:27939791 | ATAAATAAATAAAAT[G/T]CAGATTCCTGAGTCC | 55130 |
| rs138831505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27842328 | ATGTGGAGAATCTCT[A/G]CACTGTATCTTTATT | 55130 |
| rs138851854 | snp | A/T | 1.64841e-05 | 0.00287085 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27935045 | TGCACAAGCACCAAC[A/T]GCTTTTGTAACATTC | 55130 |
| rs138855439 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | ARMC4 | GRCh38.p7 | 10:27863563 | GTGGATCGACTTTAT[A/T]TATTCTTTTGCCATG | 55130 |
| rs138901901 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27818684 | ATAGATTGCTAGCTA[C/T]AGCAACTCCACCTAA | 55130 |
| rs138913516 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27911214 | GTGGCACTAAACAGA[C/T]TGCCAAATGGACAAG | 55130 |
| rs138924660 | snp | C/T | 8.2392e-05 | 0.00641788 | missense | ARMC4 | GRCh38.p7 | 10:27944865 | ATCAGCACTTCCAGG[C/T]CTCCAACATCTCTGA | 55130 |
| rs138945385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27876945 | CTTACAGATACTTCC[C/T]CCATTAATTCTTGAG | 55130 |
| rs138950490 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27964321 | ATCTTGGCTCCTAGA[-/T]GAGCTGGGGTAGTCT | 55130 |
| rs138963733 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ARMC4 | GRCh38.p7 | 10:27817927 | TTTATGAAATTTAGA[C/T]GATTTCTTCTAGATA | 55130 |
| rs139019850 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27943530 | GTTGGCTCACACCTG[A/T]AATCCCAGCACTTTC | 55130 |
| rs139089032 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27813339 | TTTATTCCTCATCAG[G/T]CTGTCAGTAGCAGTT | 55130 |
| rs139111655 | snp | A/G | 0.00517822 | 0.0506191 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:28000095 | TAGCTGGGATTACAA[A/G]AATGCGCCGCCATGC | 55130 |
| rs139137200 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27897545 | CCATCCACACTGCCA[C/T]GGTGTTAGGTCAAAT | 55130 |
| rs139152212 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27900376 | AAACCAGCACAAAAA[G/T]GCTGAAAATTCCAAA | 55130 |
| rs139154351 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ARMC4 | GRCh38.p7 | 10:27962560 | ACAGCAATAACATGA[A/G]CATAATCAGGTTCAG | 55130 |
| rs139170130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27854713 | GTGAGCCCAGATCGC[A/G]CCACTGAACTCCACC | 55130 |
| rs139175094 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARMC4 | GRCh38.p7 | 10:27948150 | AAGACTGACAATTTA[C/T]AGTTATCATCAAGAA | 55130 |
| rs139201510 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27844752 | AAAACAAAAACGATA[C/T]GACTTCCATTATTAT | 55130 |
| rs139206744 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27909368 | CAATTAACTTTAAAA[C/G]AAGTTATAGACAAAA | 55130 |
| rs139218220 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27886919 | TGTCACTATAAAAAG[A/T]TCAACTAAGCACAAA | 55130 |
| rs139222209 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | ARMC4 | GRCh38.p7 | 10:27950459 | GAGAGAATACTGTTT[C/G]CCGAAGAAAAATATA | 55130 |
| rs139234153 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | ARMC4 | GRCh38.p7 | 10:27830211 | CACCTCCTGGTTTCC[C/T]GGAATGTCTTTCTCA | 55130 |
| rs139253028 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27990907 | TTAAAAATAAAATAT[A/G]GCAATATTATAGCAC | 55130 |
| rs139270100 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27845630 | ACACAGACTGACAAA[C/T]TGGATGAAGAGTCAG | 55130 |
| rs139286144 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ARMC4 | GRCh38.p7 | 10:27952549 | TCCTAATGCTTGCCC[A/G]TCCCCTTTCCCTGAC | 55130 |
| rs139289946 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | ARMC4 | GRCh38.p7 | 10:27916623 | TGACCAAGATGAAGA[A/T]CTTTATGAAGATTCA | 55130 |
| rs139294349 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984108 | CCTTCTCTTGTAATG[G/T]AGACATTGAAAGCAT | 55130 |
| rs139300652 | in-del | -/AAACAAAC | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27971008 | AATAAATAAATAAAT[-/AAACAAAC]AAACAAAATAAAATA | 55130 |
| rs139336212 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27814470 | ATGTCTGCCCTCTCA[A/G]TTCCTTGGCCTGCCA | 55130 |
| rs139354142 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27921195 | TGATCTAAAGAACAC[A/G]AAATTTGGAGGATCG | 55130 |
| rs139417963 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27936107 | TTAAATGGTCGGGAC[A/G]TGAATCTCTTGTTAA | 55130 |
| rs139418327 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ARMC4 | GRCh38.p7 | 10:27817370 | ATTTTGGATATATTT[C/T]GAGGGTACAAGTGCA | 55130 |
| rs139420356 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27889278 | GGAAGATTTCACACT[C/T]GGGGTAGTTGCTAAA | 55130 |
| rs139429522 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | ARMC4 | GRCh38.p7 | 10:27875581 | GGTTCCAAGATGGCC[A/G]AATAGGAACAGCTCC | 55130 |
| rs139446159 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27977754 | AATAGACACTTTACC[A/C]CATAGGATATGTGAA | 55130 |
| rs139447864 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27941982 | CTCCTGGTCTAATTA[C/G]TTATGGCCCCAGGAA | 55130 |
| rs139490509 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27973111 | TCTACAGAAACTCCT[C/T]ATATATATTGAATAA | 55130 |
| rs139513498 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944503 | AAATTCCGAGTATAC[A/C]TAAAATCCTTCCCCA | 55130 |
| rs139514540 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27961276 | ATGTTATTTCTTCCA[C/T]ACCATACTACAAATC | 55130 |
| rs139517333 | snp | C/T | 0.000264166 | 0.0114897 | missense, utr-variant-3-prime | ARMC4 | GRCh38.p7 | 10:27936858 | AGCCTAACGAGGTCC[C/T]GGGTTTCCTTATCTT | 55130 |
| rs139520177 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | ARMC4 | GRCh38.p7 | 10:27875398 | TTCCGTTGCTGGAGA[A/G]GAGCTGCGTTCCTTT | 55130 |
| rs139535095 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27979043 | GGTGAAACCCCATCT[C/T]TACTAAAAATCTAAA | 55130 |
| rs139571708 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27839269 | TATATAAGTAACAAT[C/T]TCTAAAAATATGACA | 55130 |
| rs139577934 | snp | C/T | 0.000428442 | 0.01463 | missense | ARMC4 | GRCh38.p7 | 10:27860767 | ACTGCTTTGTGCTCA[C/T]CGAAGGCCACTCTAT | 55130 |
| rs139584290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27820021 | TGAATGCTACTCACG[C/T]TCATGGTGATTCTTT | 55130 |
| rs139589698 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27894873 | CCCGGCTTCAAATGA[A/C]ATTTTTGTTTCACTC | 55130 |
| rs139598627 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27913440 | CTCCAGCTCTATGCA[G/T]GTTGTTGCAAAAACA | 55130 |
| rs139602567 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27978515 | AGGAAAACTGGAGCC[A/G]GGCATGGTGGCTCAC | 55130 |
| rs139635404 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27825030 | ACTCCTAATCCTCCC[C/G]TTTCAAACCTTATTT | 55130 |
| rs139636313 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27877804 | CCTTAATAATAACAA[C/T]GATAGTAAAAATAAC | 55130 |
| rs139638929 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ARMC4 | GRCh38.p7 | 10:27978808 | AAAAAAGAAAAGAAA[A/G]GGAAAACTGAATAGA | 55130 |
| rs139675333 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27866189 | CACTGTTTAATCCTA[A/G]TTACCCTTTGAGGCA | 55130 |
| rs139679146 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | ARMC4 | GRCh38.p7 | 10:27903369 | GCAAAAGCTGTAAGC[A/T]TTCCCTTTGAAAACC | 55130 |
| rs139685659 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27930951 | CTTTTCACTCCGAAA[C/T]GTCTACGAAATGGCT | 55130 |
| rs139724964 | snp | C/T | 0.00153558 | 0.0276664 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27995116 | GGCAGCAGTCCACTG[C/T]GTCAATTTCCTCAGA | 55130 |
| rs139726879 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27917219 | AACTAGAAATCAATA[A/G]CAACATGGGATCTGG | 55130 |
| rs139732355 | snp | A/G | 0.217851 | 0.247924 | intron-variant | ARMC4 | GRCh38.p7 | 10:27906250 | ATGCGACCAACAAAC[A/G]TATGAAAAAAAGCTC | 55130 |
| rs139741736 | snp | A/C/T | 0.000131833 | 0.00811802 | missense | ARMC4 | GRCh38.p7 | 10:27860704 | GCCTGAGCTGTCGCC[A/C/T]GATGCACGTTGGTGT | 55130 |
| rs139758685 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | ARMC4 | GRCh38.p7 | 10:27869661 | TGGCTTAGCCTCCCA[A/G]GTAGCTGGGATTACA | 55130 |
| rs139831826 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARMC4 | GRCh38.p7 | 10:27817048 | AGCCACCGTGCCCGG[C/T]CTGTTATGCAGTTTT | 55130 |
| rs139852646 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | ARMC4 | GRCh38.p7 | 10:27922354 | TCCAAACTAAGACTA[C/T]AGAACTTAAGCTAAT | 55130 |
| rs139863982 | snp | C/G | 0.0197687 | 0.0974348 | intron-variant | ARMC4 | GRCh38.p7 | 10:27870409 | GTGCTCAACATGCAG[C/G]TTTGTTACATATGCA | 55130 |
| rs139906731 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27889776 | ACGGTTAAGCAGCCC[C/T]GTGACCTCAGTTTTG | 55130 |
| rs139914602 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27952439 | ACATGTGCAGAACGT[A/G]CAGGTTTGTTACATA | 55130 |
| rs139919116 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ARMC4 | GRCh38.p7 | 10:27927759 | CGCTCAACTCTCTGG[C/T]TGATGCCTGTTTCTT | 55130 |
| rs139921169 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27860490 | AACACATGGCTTGAA[G/T]GCAGCCATGATGCAG | 55130 |
| rs139934178 | snp | A/G | 4.94409e-05 | 0.00497172 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27860712 | TGTCGCCCGATGCAC[A/G]TTGGTGTCATTTGAT | 55130 |
| rs139947375 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27955483 | GACTCAGTCCTGGCC[A/T]GCAGCTCCCTTCTGT | 55130 |
| rs139977682 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27850789 | ATCAGACAACAAAAG[A/T]CAGTGATTCTTGAGA | 55130 |
| rs140009630 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27966455 | ATTTTAAAAAGCAGC[G/T]CCCCAAAGAAAAGCT | 55130 |
| rs140055061 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27985593 | GAAGAATCATCACTA[C/G/T]AACTATATGTGCATG | 55130 |
| rs140095690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27993371 | AATAAGATTTCAGGC[C/T]GGGCGTGGTGGTTCA | 55130 |
| rs140152614 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27941256 | TAGGAGCTCGAGGTG[A/G]GAGGATCACTTGAGG | 55130 |
| rs140153681 | snp | A/G | 0.031825 | 0.122064 | intron-variant | ARMC4 | GRCh38.p7 | 10:27900990 | TACTCCTCGAGAAGA[A/G]CAACCCCAAGACACA | 55130 |
| rs140153798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27831102 | GATCTGGAGGCCAAC[A/G]GCCCAGGAGACAGTG | 55130 |
| rs140186220 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27833975 | GCGGTGAAGGTTCCA[C/T]ATGGCGCCACCTTAC | 55130 |
| rs140213696 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27959280 | AAAGGAAAGGAAAGG[A/G]AAGGAAGAAAGGAAG | 55130 |
| rs140232110 | snp | C/T | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27964270 | TGGTTAGTGAAGTGG[C/T]TGTGCTAAAACACAT | 55130 |
| rs140265397 | snp | A/T | 5.18677e-05 | 0.00509226 | intron-variant | ARMC4 | GRCh38.p7 | 10:27862419 | GCATGTAAAACAAAA[A/T]GATGTGTTACTTACT | 55130 |
| rs140271845 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, missense | ARMC4 | GRCh38.p7 | 10:27836020 | AAGGTCTTCATCCTC[G/T]TCATCTTCCCGTTGA | 55130 |
| rs140298890 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARMC4 | GRCh38.p7 | 10:27823222 | ATTAAATATAAAGAA[C/T]ATTGGCACACATAGG | 55130 |
| rs140299927 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | ARMC4 | GRCh38.p7 | 10:27932465 | TTAAGAAATTAATAG[C/T]CACAGAAAGATTAAA | 55130 |
| rs140322529 | in-del | -/TGTCTATGA | 0.166596 | 0.235677 | intron-variant | ARMC4 | GRCh38.p7 | 10:27939395 | AATGGTTCTTAGACC[-/TGTCTATGA]AAATCCAATGGAGTT | 55130 |
| rs140338410 | snp | A/G | 9.96165e-05 | 0.00705679 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27939915 | GTAAATGGCCATGGC[A/G]CAGTGCTCCTGCAGC | 55130 |
| rs140342792 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27843988 | GAGGATTGCTTGAGG[A/C]TGAGTTCAAGACTGA | 55130 |
| rs140344562 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ARMC4 | GRCh38.p7 | 10:27908833 | TAAAATTGGTGACGC[C/T]GAAAAAGAGCATTGA | 55130 |
| rs140409453 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ARMC4 | GRCh38.p7 | 10:27938448 | CTCAGAAGAAACTAA[C/T]TTTGGTCTGAAACGT | 55130 |
| rs140501084 | snp | A/T | 0.0260105 | 0.111035 | intron-variant | ARMC4 | GRCh38.p7 | 10:27848281 | TACACATCTACAACC[A/T]TCTGATCTTTGACAA | 55130 |
| rs140512387 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | ARMC4 | GRCh38.p7 | 10:27942452 | TTAGTCTATAGGAAA[A/C]CTGGTTTTGTTACAT | 55130 |
| rs140546485 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27928251 | CCCAAGCCAGCAAAC[C/T]GAACATCATCTACGA | 55130 |
| rs140548414 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27996576 | AAGTGAAAAACTTCA[A/G]ATAAGCACTACCTGA | 55130 |
| rs140569195 | snp | C/T | 0.000896535 | 0.0211533 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27944256 | TGCTGCCTCACCACC[C/T]GCCGTGCTCTTTTAA | 55130 |
| rs140575451 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ARMC4 | GRCh38.p7 | 10:27910493 | AGGCACGGTGGCTCA[C/T]GCCTGTAATCCTAAC | 55130 |
| rs140577392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27975873 | AGCTACACACTAATA[A/G]CTTTATGAATATAGG | 55130 |
| rs140579826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27895866 | TCTACTCCTGAAGTA[C/T]CCTTCTGCCTTGGAA | 55130 |
| rs140589545 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27980367 | AAAAATGTTTCTGCA[A/T]CAAAGGACACTATCA | 55130 |
| rs140601894 | snp | A/G | 1.6743e-05 | 0.0028933 | synonymous-codon, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983843 | TAAAAATTTACTTAC[A/G]CCATTTAAAAATACT | 55130 |
| rs140623111 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | ARMC4 | GRCh38.p7 | 10:27913796 | AGATACTATCTCACA[A/T]GAGTCGGAATGGCTA | 55130 |
| rs140624045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27876216 | TTCTCCCAGCACAGA[A/G]TTTGAGATCTGAGAA | 55130 |
| rs140634025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27945075 | TGAGTGGGCTAGAAT[C/T]TGTTAAATGAATCAG | 55130 |
| rs140638998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27946625 | GGAACTTGAACTTAG[C/T]TGTACTATCTCACTG | 55130 |
| rs140657175 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | ARMC4 | GRCh38.p7 | 10:27861309 | AGGAACTAGACTTTT[C/G]GTGGGTCACCAACAG | 55130 |
| rs140682249 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27867708 | TAATCTCAGCACTTT[A/G]GAAGGCTGAGGCAGG | 55130 |
| rs140694082 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | ARMC4 | GRCh38.p7 | 10:27932917 | CCATTATAAATCCAG[C/T]GGCTAGCACAAAAGA | 55130 |
| rs140699432 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27895411 | TGATTCTTGTGCCTC[A/C]CAAGTAGCTGGGATT | 55130 |
| rs140701635 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27998136 | TTCTTTAGGGGGCTA[C/T]GGAAAGGCAGCCATC | 55130 |
| rs140762837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27898076 | ACAGAACACACTTTA[C/T]ATATAATAATAGCAC | 55130 |
| rs140804650 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | ARMC4 | GRCh38.p7 | 10:27958099 | CATTTATAGATATAC[C/T]TTTCCTTTTATTGGC | 55130 |
| rs140804892 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:28000341 | TACTACCTGCAGAGA[A/G]GCTTAGACTTGCAAC | 55130 |
| rs140819201 | snp | A/T | 0.0640965 | 0.167152 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872605 | CTTTCCTGCATCCAT[A/T]GAGATAATCATGTGG | 55130 |
| rs140819551 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27855181 | CAATTATTCCTTAAA[G/T]CTGTCAAGATCTCTT | 55130 |
| rs140854078 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | ARMC4 | GRCh38.p7 | 10:27899577 | TGGCTTGAAATTCTC[A/G]CTGTGAGCATAGCAG | 55130 |
| rs140882012 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27843842 | GCAATATACATAAAG[A/C]TTTGTTTTTTCAAAA | 55130 |
| rs140929878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon | ARMC4 | GRCh38.p7 | 10:27858197 | TTCTACCAACACCCA[A/G]TATGCCACACCCACA | 55130 |
| rs140937918 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | ARMC4 | GRCh38.p7 | 10:27963770 | CATATAATATATATT[A/G]TATGAATTTCATTAC | 55130 |
| rs140950719 | snp | C/T | 4.94743e-05 | 0.0049734 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27944371 | AGCCCCCAAGGTCAA[C/T]AATATTCTGTCTGAT | 55130 |
| rs140969989 | in-del | -/A | 0.496999 | 0.0386216 | intron-variant | ARMC4 | GRCh38.p7 | 10:27848539 | AAAAACAATGGTAAC[-/A]AAAGCCAAAATTGAC | 55130 |
| rs140990425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27814729 | TTAGATTGCATAGTC[C/T]GTCTTTTGAATCATT | 55130 |
| rs140992303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27845038 | AGCAAGGCAGGCCAA[C/T]ATTCAAATTCAGGAA | 55130 |
| rs141010457 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27970384 | TGATTAGCTCCATAT[A/C]ATTTTCATCATTCCA | 55130 |
| rs141047706 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27996161 | GATAATCTATACTTG[C/T]TTCTTTTCTCTTTTG | 55130 |
| rs141066040 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27856627 | GGAATTGCACAGTCT[A/G]GCAAGGAAACCGCTA | 55130 |
| rs141080754 | snp | A/T | 0.021333 | 0.101051 | intron-variant | ARMC4 | GRCh38.p7 | 10:27950028 | ATTGATCAGGACCAG[A/T]GGCCTCTTGTTCTGT | 55130 |
| rs141082838 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27925092 | AAAAAGAAAAACTAC[A/G]GACCAATATCACTCA | 55130 |
| rs141109726 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ARMC4 | GRCh38.p7 | 10:27831663 | GATGGCCTCCCTTGG[C/T]GTACGTGCCCACACA | 55130 |
| rs141113205 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARMC4 | GRCh38.p7 | 10:27911090 | TTTTTCCAAAAGGAA[C/T]ATCGCCGCCGTCCTG | 55130 |
| rs141178036 | in-del | -/T | 0.141258 | 0.225111 | downstream-variant-500B, intron-variant | ARMC4 | GRCh38.p7 | 10:27811670 | GATAAAATGCTATTT[-/T]GTTTTGTAGCCACTT | 55130 |
| rs141182393 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ARMC4 | GRCh38.p7 | 10:27893216 | AAGAGAAAAGAAATA[A/G]AGAAAAGATGTTCTA | 55130 |
| rs141214243 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | ARMC4 | GRCh38.p7 | 10:27979399 | TTTGTATGCAGATGG[A/C]ATGATCTTGTATGCA | 55130 |
| rs141255601 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27930008 | TCTTGAGGAATACCA[A/G]TTACGTTTATGTTGG | 55130 |
| rs141305156 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27824557 | TTTTTCCTCATAAAT[C/T]ACCCAGTCTATATTC | 55130 |
| rs141309281 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27948592 | TTCACATTTTATCAC[A/G]CATTTGCATTTCTGA | 55130 |
| rs141309423 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27841801 | GCTCTGTCATTCAGG[C/T]TGGAGTATGGTAGTG | 55130 |
| rs141324736 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983741 | TTCTATCCCACAGAA[C/T]GGTAATTCATTCTCT | 55130 |
| rs141397236 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | ARMC4 | GRCh38.p7 | 10:27867864 | TGAGGCATGAGAATC[A/G]CTTGAACCTGGGAGG | 55130 |
| rs141403979 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27842738 | TGATTGATTAAAATT[C/T]TGAACAAACAAAATA | 55130 |
| rs141415065 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | ARMC4 | GRCh38.p7 | 10:27869471 | CTGGTACAACTTCTG[A/G]ACTTAAAAAAAAAAA | 55130 |
| rs141442431 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27830063 | CTGAACAGAAAGTAG[C/G]GCACAGGATGGTGGA | 55130 |
| rs141454045 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | ARMC4 | GRCh38.p7 | 10:27871810 | CTGCAGCTGTGTTCT[G/T]TGGACTTAGGATTGT | 55130 |
| rs141461520 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27976947 | TCACAGACAAATGAA[C/G]GACTAATTTTTGACA | 55130 |
| rs141463220 | in-del | -/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27973924 | GTATTCCCTTTTTTT[-/C]TGCAACTTCACCAGC | 55130 |
| rs141504921 | snp | C/T | 3.29641e-05 | 0.00405968 | missense, utr-variant-3-prime | ARMC4 | GRCh38.p7 | 10:27936808 | TATTGTCAGTGTTAT[C/T]GAGTAGACTGGCCAA | 55130 |
| rs141508372 | in-del | -/T | 0.138886 | 0.22395 | intron-variant | ARMC4 | GRCh38.p7 | 10:27877489 | CCCTGCAGGTCCCTC[-/T]GAAGTTTATTTGTTT | 55130 |
| rs141509512 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | ARMC4 | GRCh38.p7 | 10:27817296 | TGGTTCAGAATTTTT[A/G]TTGATCTCTTTGTTT | 55130 |
| rs141523836 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27858624 | TCTAAAGTTTCTCTT[C/T]ACAGAAACTTTCCTA | 55130 |
| rs141527849 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | ARMC4 | GRCh38.p7 | 10:27925008 | AAAAAAAAAAATCCC[A/G]ATTCCTTTTGTGAAG | 55130 |
| rs141528740 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27815419 | GAATTCCTATCTCCA[C/G]TCTTAAATTCCATCC | 55130 |
| rs141528772 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27855815 | CTGCCAATGCTGGAC[A/G]TACTTCTGATTGTAT | 55130 |
| rs141587142 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27881133 | TTAAAAGGATACATA[C/T]TAAGCATACAGCAAG | 55130 |
| rs141589813 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27819530 | GATGGCTTGAAGCCA[C/G]AAGTTCAAGACCATC | 55130 |
| rs141592719 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27817928 | TTATGAAATTTAGAC[A/G]ATTTCTTCTAGATAC | 55130 |
| rs141599016 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ARMC4 | GRCh38.p7 | 10:27969289 | GTGAATCCTGCACCC[A/G]ATGCCTTCTACTCTA | 55130 |
| rs141666010 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | ARMC4 | GRCh38.p7 | 10:27920112 | AAAAAAAGAGATATC[C/G]CCAGAGTAGAGAGAG | 55130 |
| rs141695606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27816582 | AACAATGCAGGAAAA[C/T]AGTTTAGGTGGGACC | 55130 |
| rs141698663 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27887115 | ATATATTATTTACAA[C/G]AGCATCATTTTAGAT | 55130 |
| rs141701048 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | ARMC4 | GRCh38.p7 | 10:27908518 | AGAAGAAGGCCAAAC[A/G]AAACTTAATAACCTT | 55130 |
| rs141703933 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27972722 | AATTAGCACACAATC[A/G]TAATTGTATATTCAC | 55130 |
| rs141744535 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ARMC4 | GRCh38.p7 | 10:27953713 | TTTCATTTATGTATA[C/T]AAATTATATATGTAT | 55130 |
| rs141757160 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27955960 | CTCTGGATTAGAGTA[C/T]TGACCACTACTAAGC | 55130 |
| rs141761522 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27858959 | CAGGTGCATGCCTAT[A/T]CATTTTTAAACTTTT | 55130 |
| rs141768122 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27925350 | ATTACCAATCCTAAT[A/G]AAAACACTTTTTAAA | 55130 |
| rs141793692 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27819753 | CTCAAAACCCATACC[C/T]TTGACTATGGTTTGA | 55130 |
| rs141823232 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | ARMC4 | GRCh38.p7 | 10:27958287 | GAAATAGTGCATCTC[C/T]TTTTGGCCTAAAGCT | 55130 |
| rs141870558 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27854692 | GCCAAGGAGGTAGAG[G/T]TTGCAGTGAGCCCAG | 55130 |
| rs141877972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27918696 | TGGCCTGCCTAATAA[A/G]GCACACACAAAAAAG | 55130 |
| rs141879964 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27853150 | GAGGCCGGCAGATCA[A/C]GAGGTCAGGAGATTG | 55130 |
| rs141942925 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27841035 | TAATTGATTGTTATT[C/T]TTTTTAAAATAGATC | 55130 |
| rs141956063 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27907921 | AAACTTCATCAACAG[C/T]AGGGAGATAACATGC | 55130 |
| rs142055856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27844235 | TAAATTAAGAATATA[C/T]ACCAGCTGCAAGAGC | 55130 |
| rs142065311 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | ARMC4 | GRCh38.p7 | 10:27937778 | TGTTTATCTTCTGCA[C/G]GTGATTTTCAATTCT | 55130 |
| rs142142849 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | ARMC4 | GRCh38.p7 | 10:27975170 | CCCTTGTTTTATATG[C/T]TCCAAGTAAAACATT | 55130 |
| rs142144475 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27941352 | AAGCTGGATGTGGTG[A/G]TGCATGTGTGTAGTC | 55130 |
| rs142167847 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27939084 | ATGAAATGTATCATA[C/T]ACAAAAAGTTAGTGT | 55130 |
| rs142231437 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ARMC4 | GRCh38.p7 | 10:27942200 | ACAATCTTTGCCTTG[C/T]AAAAATTTATTCCTT | 55130 |
| rs142231488 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27901960 | AACAAGCGAACCTAA[C/T]AGACATCTACATAAC | 55130 |
| rs142239206 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27882808 | AAAACTGCCTGTATG[C/G]CAATTCCTAGGAAAA | 55130 |
| rs142240280 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | ARMC4 | GRCh38.p7 | 10:27947891 | CTTGACTGCTATTCT[G/T]GCATTATAATGTTTT | 55130 |
| rs142262003 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | ARMC4 | GRCh38.p7 | 10:27837692 | GAACGACAAAATAAA[A/C]TTTATAAATATTTCT | 55130 |
| rs142272195 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ARMC4 | GRCh38.p7 | 10:27906039 | AATTAAACTAAAAAG[C/T]TCTGCACAGCAAAAG | 55130 |
| rs142294597 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ARMC4 | GRCh38.p7 | 10:27835745 | GCCTGTCCAACATGG[C/T]GAAACACTGTCTGTA | 55130 |
| rs142296807 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27903994 | CAATCTATGTTTTCT[C/G]CAAATAAGGACTACC | 55130 |
| rs142328573 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27990400 | ATGCTGGCCTTGAAC[C/T]CCTGGGTTCGAGTGA | 55130 |
| rs142341588 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ARMC4 | GRCh38.p7 | 10:27896614 | TTAGGCATTCTAGAA[C/T]CATCCTTTTGCTTGG | 55130 |
| rs142349917 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27849852 | ATTCTTTTTAAAGTC[A/G]CAAAAGCTACTCTAA | 55130 |
| rs142368598 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27890063 | AATAAAAAATGCATA[A/G]TCAAAAAAATGGAGC | 55130 |
| rs142368914 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27817808 | CACATACAAGTGCAG[G/T]TATGTTTTTGACACC | 55130 |
| rs142412128 | in-del | -/AATG/GAAT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27970134 | ATAAATAAATAAATA[-/AATG/GAAT]AATAAATAAATAAAT | 55130 |
| rs142415372 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27854004 | TACACATATGGTAAG[A/C]AACCAGAATGTATAC | 55130 |
| rs142477186 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | ARMC4 | GRCh38.p7 | 10:27821591 | CCTGAATTTGATGTG[A/G]AGCTAATATAAATGA | 55130 |
| rs142516325 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27903825 | TCCTCTGAAAAGCTG[A/G]TGTCACAGGCTGCCT | 55130 |
| rs142524360 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ARMC4 | GRCh38.p7 | 10:27919689 | GTAGGAGTGTAAAAT[C/T]GTACAATCACTTTTG | 55130 |
| rs142543096 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27987251 | TTTCATGAAGTTGTA[C/T]ATTTGACTTTTTACC | 55130 |
| rs142544691 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27867457 | ACACGGAATAGCATC[A/T]TCCAAATTGAGCAAC | 55130 |
| rs142565071 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | ARMC4 | GRCh38.p7 | 10:27921227 | TTGAGCCCAGGAGTT[A/T]AAGGCTGCAGTGACC | 55130 |
| rs142588104 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27886471 | CTAGAGAAACAAGTT[G/T]AAGGATTTATTACTA | 55130 |
| rs142598573 | snp | A/G | 0.000115355 | 0.00759368 | missense | ARMC4 | GRCh38.p7 | 10:27940664 | TGCCCCCAGCTTTGC[A/G]GATGGCTTCTTTATT | 55130 |
| rs142600219 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | ARMC4 | GRCh38.p7 | 10:27923526 | GTACATTAATAATAA[G/T]AGAATTTCATACAGC | 55130 |
| rs142642181 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27818147 | TCCTGATATTCATAT[A/G]TCTCTATGCCCAATG | 55130 |
| rs142656895 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27891228 | ATACTCAGTCCTCAA[C/T]ATTCCTGGCTAAATT | 55130 |
| rs142689838 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | ARMC4 | GRCh38.p7 | 10:27894359 | CACGGATATACATTT[A/T]CATGTATCTTTGGTC | 55130 |
| rs142700404 | snp | C/T | 0.110167 | 0.207236 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872327 | TTGACTTCCTCTTTT[C/T]CTAATTAAATACCCT | 55130 |
| rs142724516 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARMC4 | GRCh38.p7 | 10:27913000 | CTTGGGATAAGTATG[C/T]CAGAAATTCTTTAGC | 55130 |
| rs142732089 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27912455 | GTTTGCTACGTTTCT[C/T]AGGCTCTTGTTATGT | 55130 |
| rs142740541 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | ARMC4 | GRCh38.p7 | 10:27977550 | CACTCCAGCCTGAGT[A/G]ACAGAGGGAGACTCT | 55130 |
| rs142754781 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27876805 | ACTGTGTTACAACTT[A/G]TCTCTATATGCATGT | 55130 |
| rs142758562 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27942800 | AATTAACATTCTGCC[A/G]CATTCGTTTTATTAC | 55130 |
| rs142760602 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27833887 | AGAGCAAATCTGAAA[C/T]CTGAAAGATGGTTAT | 55130 |
| rs142765382 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | ARMC4 | GRCh38.p7 | 10:27915093 | AGGTCCAAGAAGCTC[A/C]GCGAACCCTAAATAA | 55130 |
| rs142766153 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27877415 | GCACAGTTCAACAGG[A/G]TCCCATAAGCTTCCT | 55130 |
| rs142773722 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27982064 | TAGATCTCTGTGTAA[C/T]GATCTGTCCACACAC | 55130 |
| rs142803772 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27864181 | GGAGAGAAGATTGTG[C/G]ATTTGGGAAGCTTGC | 55130 |
| rs142857852 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27895111 | TACAGGTGATTTTTT[A/T]AATTTGCTTTTCTTT | 55130 |
| rs142860885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27956533 | GTGCCTGGACAATAC[A/G]GGCATCTTATCCTGT | 55130 |
| rs142893680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27945651 | TTAAAAAACAAAACC[C/T]AAAAGATTAAAAATA | 55130 |
| rs142922886 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27838259 | TACCATTATTAGTAG[G/T]AGTAATTCTTACATT | 55130 |
| rs142931097 | snp | C/T | 0.0170251 | 0.090679 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999149 | CACTTTTATTCAACT[C/T]TGCATCTCCCTTTCT | 55130 |
| rs142933661 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27909582 | CAACACTTTGAGAGG[C/G]GAAGGCAGGCAGATC | 55130 |
| rs142938724 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27976213 | AGACCATTTCTATTC[-/A]ATTTTTTACTGGTGA | 55130 |
| rs142960463 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27898758 | GTATTGATATTGACG[A/G]ATACATTGCCAAAAT | 55130 |
| rs143031478 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27936571 | TCTATTCTTTTCTTT[A/T]CTATTCTAAGAATCC | 55130 |
| rs143059966 | snp | C/T | 0.000280711 | 0.0118438 | missense | ARMC4 | GRCh38.p7 | 10:27935233 | CCACCAAGGTTTCAA[C/T]GGCTTTGTATTCCCG | 55130 |
| rs143064950 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27831587 | TGCCCAAAGTTGCAG[A/T]TCTTGGCAAAGTCAG | 55130 |
| rs143071015 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27924025 | GAAAGAAAGAAAGAA[A/G]GAAAGAGAAAGAAAG | 55130 |
| rs143072735 | snp | A/G | 9.88826e-05 | 0.00703076 | missense | ARMC4 | GRCh38.p7 | 10:27860705 | CCTGAGCTGTCGCCC[A/G]ATGCACGTTGGTGTC | 55130 |
| rs143073128 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27992642 | TGCAGTGAGCTATGA[A/T]CACTCCACTGCAGTC | 55130 |
| rs143079581 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ARMC4 | GRCh38.p7 | 10:27962599 | AGTTAACCACCAACT[C/T]TGAGAGACATTACCA | 55130 |
| rs143091124 | snp | C/T | 0.0640965 | 0.167152 | intron-variant | ARMC4 | GRCh38.p7 | 10:27874480 | TTTGGCATGTTTTTG[C/T]AGTGGCTGGTACCAG | 55130 |
| rs143095231 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27818923 | GTTTTGAGGTCACAG[C/T]ATCTTGGATCTGTAC | 55130 |
| rs143096939 | snp | A/C/T | 0.000215336 | 0.0103743 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940550 | GCAAGGGAAGCAGAA[A/C/T]TGGCATGAGTACCTC | 55130 |
| rs143104659 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27892765 | TATTTCTCTCAATTA[A/T]CCTGTAATTCATTAC | 55130 |
| rs143140554 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27942316 | TCTTTCTTAAATGTA[C/T]GTATAGGTCACAGTC | 55130 |
| rs143145244 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27965839 | TATAAAAAGACTTAC[A/G]AGAAAGTACACTTTA | 55130 |
| rs143146880 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ARMC4 | GRCh38.p7 | 10:27860184 | TGGCTGGGCATTGTG[A/G]CTCACTCCTGTAATC | 55130 |
| rs143165374 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | ARMC4 | GRCh38.p7 | 10:27835895 | TGCACCACTGCACTC[C/T]AGCCTGGGTGACAAG | 55130 |
| rs143177541 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27863497 | TTGAGTAGGGGGTTA[A/C]AAGTAAATTTGAGCA | 55130 |
| rs143209791 | snp | A/G | 1.64993e-05 | 0.00287218 | missense | ARMC4 | GRCh38.p7 | 10:27862480 | ACTCCATGATCTGTG[A/G]TAACAGCTAAATTTT | 55130 |
| rs143213104 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27979504 | GTGAAGTTGCGAAAT[A/T]CAATCTTGATTTTAA | 55130 |
| rs143215183 | snp | C/G | 0.00324298 | 0.040137 | missense, utr-variant-5-prime, intron-variant | ARMC4 | GRCh38.p7 | 10:27981519 | CTCTTAAAAATGTGA[C/G]AAGGTTTTTATAAAT | 55130 |
| rs143237949 | snp | C/T | 0.0722614 | 0.17581 | intron-variant | ARMC4 | GRCh38.p7 | 10:27901544 | AAGATCAAGACCCAC[C/T]GGTGTGCTGTATTCA | 55130 |
| rs143242599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27880641 | AAGAGGCTACACATA[A/G]CAAGAGGCCCTATTG | 55130 |
| rs143244885 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27904977 | ATATTGTTTGTGTTT[A/T]TCAAGGCCATTGATT | 55130 |
| rs143253808 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | ARMC4 | GRCh38.p7 | 10:27969271 | CAGGCTGCCACTGTT[A/G]GTGTGAATCCTGCAC | 55130 |
| rs143254607 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | ARMC4 | GRCh38.p7 | 10:27963838 | TGGCCACAAGAGTTC[A/C]GGACAACAGACTGTG | 55130 |
| rs143299831 | in-del | -/ATAA/ATAAATAA/ATAAATAAATAA/ATAAATAAATAAATAA | 0.437782 | 0.195877 | intron-variant, splice-acceptor-variant | ARMC4 | GRCh38.p7 | 10:27853365 | GGCGAGACTCTGTCT[lengthTooLong]ATAAATAAATAAATA | 55130 |
| rs143338168 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | ARMC4 | GRCh38.p7 | 10:27811844 | TTGTTTATGCTCTGT[A/G]AGTCAAAGTGTAAAA | 55130 |
| rs143338979 | snp | C/G/T | 0.00201548 | 0.0316812 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27994945 | ACCTGATTCAAATGC[C/G/T]GAGGGCGCCAAACTT | 55130 |
| rs143347478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27816225 | GTCTGATGAACTATT[C/T]ATACTGTATCTAGAG | 55130 |
| rs143362054 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27998157 | GGCAGCCATCAGCTC[C/T]GAGATCTATGAAATG | 55130 |
| rs143385112 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27954312 | CATATTTTAAGGAAC[-/A]AAAATAAGTGTTGTT | 55130 |
| rs143391103 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ARMC4 | GRCh38.p7 | 10:27913709 | AAAGAAGACATACAC[A/G]TGGCCAGCAAGCATA | 55130 |
| rs143417335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27914108 | AATGGTAGACTGGAT[A/G]AAGAAAATGTACATA | 55130 |
| rs143430293 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27982916 | CACCCAGCCTCTACT[C/T]TGTGCTACTCACGCA | 55130 |
| rs143437137 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27850887 | TACAGCACAGGGAGG[C/G]AGAGCCCAGACAAAG | 55130 |
| rs143455968 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | ARMC4 | GRCh38.p7 | 10:27916165 | GACTGAAAAGTGTGA[A/C]AGAAAGTGCCAATAT | 55130 |
| rs143495131 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ARMC4 | GRCh38.p7 | 10:27947075 | TATTTACTAATAAGT[C/T]ATGTTCTTACAGCTT | 55130 |
| rs143503258 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ARMC4 | GRCh38.p7 | 10:27813884 | AATAAAAGGTAAGGA[C/T]AGTGAGGAAGGAACA | 55130 |
| rs143513621 | snp | C/T | 0.000234349 | 0.0108222 | missense, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27961677 | TCACTTTCTGAGGAG[C/T]TATCGCTAACAGTTT | 55130 |
| rs143523047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27853900 | AAAAATAAATTGGAC[C/T]TCACCAGCGTTAAAA | 55130 |
| rs143554548 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27907219 | GAAAAGTGAGAGTCA[C/G/T]TGAAATCATGTGACC | 55130 |
| rs143555276 | snp | G/T | 0.0501905 | 0.150254 | intron-variant | ARMC4 | GRCh38.p7 | 10:27841639 | GACCTCAGGTGATCT[G/T]CCTGCCTCGGCCTCC | 55130 |
| rs143596323 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ARMC4 | GRCh38.p7 | 10:27899788 | CTCTGGGCAGGGCAT[C/T]TCTGAAAGAAAGGAA | 55130 |
| rs143608110 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27828731 | AATAATTTTGTTTTG[C/G]TTTATAACTTTACTC | 55130 |
| rs143631008 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27949824 | AAGTAACTTGGAGTA[A/G]GAGGGGAGGGTGACT | 55130 |
| rs143673800 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27832459 | CTTTCTCTCTTGTCC[C/T]TTGTATCGCAGCCAG | 55130 |
| rs143680875 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27949071 | GAACAATGCCCCTCC[C/T]TTACCATTGATAAGG | 55130 |
| rs143748869 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27910119 | AATAACTTGGTTTTC[C/T]GTCCTCAGTTTTTCT | 55130 |
| rs143781230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27977793 | AAGCACATGAAAAGA[C/T]GCATTCAAGAACTGC | 55130 |
| rs143814410 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27986819 | CACATATTTTTAAGA[A/G]GAAGAAAAATATTTG | 55130 |
| rs143839144 | snp | A/T | 0.0166325 | 0.0896639 | intron-variant | ARMC4 | GRCh38.p7 | 10:27885447 | CCTGGGAGGTGGAGG[A/T]TGCAGTGAGCCAAGA | 55130 |
| rs143851876 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27915885 | ACAATATGGACACAA[A/G]CTGTTCACATTTGTT | 55130 |
| rs143852893 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27983085 | GAGTCACCCCAGCAA[C/T]GGCCCTTCTTTCCAC | 55130 |
| rs143874747 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27813804 | CTCTTACAGCAAATT[A/G]TATAGACTGTAGAGA | 55130 |
| rs143885806 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | ARMC4 | GRCh38.p7 | 10:27882221 | AAAGAAAGAAAGAAA[G/T]AAAGAAAGAAAGAAA | 55130 |
| rs143900870 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997830 | ATTGCCAAGCTCTTT[C/T]GGCTTAAGAACCATA | 55130 |
| rs143922387 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | ARMC4 | GRCh38.p7 | 10:27825089 | CAACTCATCTCTCTA[C/G]TTGCTTGGGCTGAAA | 55130 |
| rs143933144 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27897728 | AGGGCAGTTCCTGGT[A/G]AGAGATGTGATCAAG | 55130 |
| rs143968716 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27812920 | TCTTGCATCTTTTCT[C/G]TCTTTTCCACCTCTC | 55130 |
| rs143981066 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27881620 | CCAACCTGGGCAACA[C/G]AGCAAAATCCCGTCT | 55130 |
| rs143993558 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27854977 | GAAAACTTATCTATA[C/T]TGACAGAAAGCAGAC | 55130 |
| rs143995165 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ARMC4 | GRCh38.p7 | 10:27921403 | AAGGATATTTTGAAG[C/T]AATGGAAAATTTAGA | 55130 |
| rs144023145 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984197 | ACCTGAGGTATATTC[A/G]ATAGATTCCAAGACT | 55130 |
| rs144037130 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | ARMC4 | GRCh38.p7 | 10:27816081 | CCTATGCTGCATCCA[A/G]CTGATTATCATATTC | 55130 |
| rs144037633 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:28000104 | TTACAAGAATGCGCC[A/G]CCATGCCCGGCTAAT | 55130 |
| rs144064189 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27937155 | GGCATCTCCTGAGGC[A/G]AAGGTCAGTGGAAAA | 55130 |
| rs144080867 | in-del | -/T | 0.143622 | 0.226238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27838761 | TACTTTATTTTACCA[-/T]TACTGTTTGTGTATT | 55130 |
| rs144091074 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ARMC4 | GRCh38.p7 | 10:27814485 | GTTCCTTGGCCTGCC[A/G]TTGTCACTGATCTTC | 55130 |
| rs144099047 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27883900 | AGAAGAAATAAATGA[A/G]GTAACATAAGCATAG | 55130 |
| rs144104950 | snp | C/T | 0.00636936 | 0.0560724 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999406 | TACCCCCAAATAGCA[C/T]AGGGCTTCTCCTAGG | 55130 |
| rs144131651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27889447 | ATATAATCATCGTAA[A/G]TGATTCTCTCACACA | 55130 |
| rs144132711 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27823366 | ATGGCAATTCTCTGG[-/A]AAAAAATATTCCCAT | 55130 |
| rs144145876 | snp | A/G | 0.000330748 | 0.0128555 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27987390 | ATTAAGATCACCTTC[A/G]ACACATGCTTGGGCT | 55130 |
| rs144191673 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | ARMC4 | GRCh38.p7 | 10:27823728 | TTGGACTGATCCAAA[C/T]AAGCAATTTTAATCT | 55130 |
| rs144204949 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | ARMC4 | GRCh38.p7 | 10:27871041 | GACTTTTTAATGATC[A/G]ACATTCTAACTGGTG | 55130 |
| rs144205002 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27908964 | CTTAAGTAAGTAGGT[G/T]TTCAAACCTAAAACT | 55130 |
| rs144218843 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ARMC4 | GRCh38.p7 | 10:27973768 | GCATGTGTCTTTATG[C/T]GATGATTTATATTTC | 55130 |
| rs144270236 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | ARMC4 | GRCh38.p7 | 10:27913851 | GATGCTGGCAAGGTT[A/G]TGGAGAAAAGGGAAA | 55130 |
| rs144274384 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27978933 | TCAGGAGTCAGGCTA[C/G]GCATGGGGGCTCACA | 55130 |
| rs144283287 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27958623 | TGAAGGCCACCTGCA[C/T]GAGTCAGTTAAGTCT | 55130 |
| rs144318239 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27946814 | CACAAGGCTTTTAAA[A/C]TAAGAAACCGAAATA | 55130 |
| rs144339366 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27917080 | ATAAAACTACTGCAG[A/T]ATACACAGTTTTCTC | 55130 |
| rs144343368 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984547 | ACACTAAAAATATTA[A/G]AAAATGAACATGCTT | 55130 |
| rs144362811 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27927299 | GTGACCCAAGTTTTT[-/A]ACCATAGCCACAGCC | 55130 |
| rs144384555 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ARMC4 | GRCh38.p7 | 10:27900947 | GGCCAACATTCAAAT[C/T]CAGGAAATACAGAGA | 55130 |
| rs144407255 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | ARMC4 | GRCh38.p7 | 10:27867111 | ATGGACAATATACAC[C/T]ATAGTAGGTGAACAA | 55130 |
| rs144407870 | snp | C/G | 0.000153988 | 0.00877328 | splice-acceptor-variant | ARMC4 | GRCh38.p7 | 10:27935253 | TTGTATTCCCGAAAC[C/G]TAAGTTCATCATAAG | 55130 |
| rs144411373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27931609 | ATGAAAAGAATATAG[C/T]TGTTTTCTCTGGCTT | 55130 |
| rs144419049 | snp | C/T | 2.19416e-05 | 0.00331215 | synonymous-codon, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27985063 | GAGGTGCAGATCCAA[C/T]TGCTTAAGCAGCATA | 55130 |
| rs144420949 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27951810 | CTGGACACAGTGGCT[C/T]ACATCTGTAATTCCA | 55130 |
| rs144474826 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27825737 | ATAAGGTTATCAGAA[C/G]CTGGAGATGTCTGTG | 55130 |
| rs144541281 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27830537 | CAGCCAAATCTTTAA[A/C]TTATGAAATTTCAAA | 55130 |
| rs144564558 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ARMC4 | GRCh38.p7 | 10:27970095 | GACAGCGAGATTCTG[C/T]CTCAAAAAATAAATA | 55130 |
| rs144571711 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27958215 | TATTGATGAATAACT[C/T]GTGCAAATTTAAGTA | 55130 |
| rs144573684 | snp | A/G | 0.00517822 | 0.0506191 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:28000449 | AGCATCACACCTGTG[A/G]CGGTAATGCAGGTCA | 55130 |
| rs144604589 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | ARMC4 | GRCh38.p7 | 10:27989546 | GAGAGGACTAAGTAA[C/T]AGGCTGACCAAATAC | 55130 |
| rs144624359 | snp | C/T | 0.00049401 | 0.0157086 | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27958876 | GAATTTCAACTCAAC[C/T]GGTCTTTCCAACGTC | 55130 |
| rs144724232 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ARMC4 | GRCh38.p7 | 10:27902592 | AAGAATCAAATAGAC[A/G]CAATAAAAAATGATA | 55130 |
| rs144735514 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27995721 | GGTTTCCCCAAGTGC[A/C]TTCTGAGTTAAAAAA | 55130 |
| rs144794309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27877015 | ATTCTCCCTTGGGAT[A/G]TAGGCTCATGTCTAT | 55130 |
| rs144802486 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | ARMC4 | GRCh38.p7 | 10:27943731 | ACCCCGTAGGCGGAG[A/G]TTGCAGTGAGCCAAG | 55130 |
| rs144838468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27931247 | TTACATATGGGTCAA[C/T]AATTCATAGCATTTT | 55130 |
| rs144842234 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27991651 | TCGGCAGAATTTCAG[C/T]GTAGATAAAACTTAA | 55130 |
| rs144911734 | snp | C/T | 0.156319 | 0.231784 | intron-variant | ARMC4 | GRCh38.p7 | 10:27899670 | TGAGTAGGTGGTTTT[C/T]CCCTCACAGTGTAAA | 55130 |
| rs144927982 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27896856 | GCTATCTTCTGGATT[A/T]CATACTAGCCTCCTT | 55130 |
| rs144934164 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27943188 | GATCTTTCCTAATGA[C/T]GGCAAAGGTGGTAAG | 55130 |
| rs144944218 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27937211 | GAGGATTTCTGCAGT[C/G]ATGCAACTCAGAGTC | 55130 |
| rs144952381 | snp | C/G | 0.0146672 | 0.084371 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27961032 | TGCTATCTGACGTGA[C/G]AGAAATGAAAATGAA | 55130 |
| rs144968343 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ARMC4 | GRCh38.p7 | 10:27895536 | TCCAGCTATTCACCC[A/G]CCTCGGCCTCCCAAA | 55130 |
| rs144970408 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ARMC4 | GRCh38.p7 | 10:27957202 | TGTCTACAAGAAAGA[C/T]GGCAGGAAAAGGAAG | 55130 |
| rs144988924 | snp | C/G | 3.29625e-05 | 0.00405958 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27860772 | TTTGTGCTCACCGAA[C/G]GCCACTCTATTCCTG | 55130 |
| rs145002194 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27946286 | GGCTTAGCACAGCTC[A/G]TGGAAATTCCATACC | 55130 |
| rs145015256 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27909716 | CCAGCTACTCAGGAG[A/G]CTGAGGCAGGAGAGT | 55130 |
| rs145018586 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27835519 | GAGTTAGGGCACCAC[A/G]CCCTCATACAGTCAA | 55130 |
| rs145021601 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27877477 | TTAGGCTCAAAACCC[G/T]GCAGGTCCCTCTGAA | 55130 |
| rs145032569 | snp | A/G | 0.031825 | 0.122064 | intron-variant | ARMC4 | GRCh38.p7 | 10:27974558 | TGCAGCCTTGTTTCT[A/G]GGCTCTCTATTCTGT | 55130 |
| rs145036456 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27841847 | GCAGCCTCGACCTCC[C/T]AGGCTAAAGTGATCC | 55130 |
| rs145040059 | snp | A/G/T | 0.00636936 | 0.0560724 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944545 | TAAGAAATCATTTCC[A/G/T]TTCCCAGAGGTTACA | 55130 |
| rs145042199 | snp | C/T | 0.000297722 | 0.0121972 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27907681 | TGCATTTTTGATGCA[C/T]GGACAGAGTGCCCAT | 55130 |
| rs145070091 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | ARMC4 | GRCh38.p7 | 10:27845042 | AGGCAGGCCAACATT[C/G]AAATTCAGGAAATAC | 55130 |
| rs145084853 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27840225 | ATTTGTACATATTTA[C/T]GTACATCTTTAAAAC | 55130 |
| rs145103626 | in-del | -/TA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27940194 | GTGTTTGTGTGTGTG[-/TA]TATATATATAGTGTA | 55130 |
| rs145133998 | snp | A/G | 0.000363216 | 0.0134713 | missense, utr-variant-3-prime | ARMC4 | GRCh38.p7 | 10:27936859 | GCCTAACGAGGTCCC[A/G]GGTTTCCTTATCTTC | 55130 |
| rs145155399 | snp | C/G | 4.94458e-05 | 0.00497197 | missense | ARMC4 | GRCh38.p7 | 10:27860784 | GAAGGCCACTCTATT[C/G]CTGCCCCACATACAG | 55130 |
| rs145157651 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27977095 | CCAAATTAAAGTGGA[A/T]CATAGATATAGATTG | 55130 |
| rs145169683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27952718 | AATGGTACCTGGGCA[C/T]AAGGGTCTTCTGTTT | 55130 |
| rs145193223 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ARMC4 | GRCh38.p7 | 10:27925182 | AAACAGTACACTATG[A/G]CTAAGTGAGACTTAT | 55130 |
| rs145204064 | snp | C/T | 0.0752113 | 0.178743 | intron-variant | ARMC4 | GRCh38.p7 | 10:27848565 | TTGACAAATGGGATC[C/T]AATTAAACTAAAGAG | 55130 |
| rs145213721 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ARMC4 | GRCh38.p7 | 10:27913922 | CTGTGAAAAGCAGTT[C/T]GGAGATTTCTCAAAG | 55130 |
| rs145258719 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27928661 | AAATAACATGTCTTG[A/T]TATAAGAGAAACACA | 55130 |
| rs145266660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997357 | TACAGAAAGGCTTAG[A/G]TGAAAGTTCTGTCTG | 55130 |
| rs145288399 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27974450 | CTTCTGCATATGGCT[A/T]GCCAGTTATCCCAGC | 55130 |
| rs145309730 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | ARMC4 | GRCh38.p7 | 10:27823412 | GTGGCTATGAGTTTA[C/T]GCTTTGAGTTCAGAC | 55130 |
| rs145311931 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | ARMC4 | GRCh38.p7 | 10:27896049 | TCAAGCGTTCACTAG[A/G]CAAGTGTCTTCAACA | 55130 |
| rs145321572 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27942073 | AAAAATTCTAAGACC[A/G]TGGGATTGAACACAG | 55130 |
| rs145324848 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27896374 | GGATCCCTTTGATAA[C/T]TTTCTCACTTCTGGA | 55130 |
| rs145356246 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27927768 | CTCTGGCTGATGCCT[A/G]TTTCTTTACAGAGAC | 55130 |
| rs145375243 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ARMC4 | GRCh38.p7 | 10:27826141 | CCAGGTTCTGGAGGA[C/T]GCAGAATGGGATCAA | 55130 |
| rs145388658 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ARMC4 | GRCh38.p7 | 10:27899317 | CGGTCTTTGCAACCC[A/G]CAGACCAGGAGATTC | 55130 |
| rs145402032 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27821207 | TCTAGAATTTTCTGT[C/G]TGCTCCGGGTATGAA | 55130 |
| rs145478988 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | ARMC4 | GRCh38.p7 | 10:27941847 | TCCACAGATACTGCC[C/T]GTAACCACCAATCTC | 55130 |
| rs145484034 | in-del | -/AAAAAAAC | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27843241 | GTCTTAAAATAAAAA[-/AAAAAAAC]CAGCCTATCTGCAAC | 55130 |
| rs145511691 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ARMC4 | GRCh38.p7 | 10:27903680 | AGAGAGCCAAATCAT[A/G]AGTGAACTCTCATTC | 55130 |
| rs145516767 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997052 | ACAACATATATGCTA[C/T]AAAAACCAAGTACTG | 55130 |
| rs145519493 | in-del | -/TATG | 0.498734 | 0.0251279 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940261 | ATAAATGTCAGTATA[-/TATG]TGTGATATATATATA | 55130 |
| rs145526722 | snp | C/G/T | 9.88805e-05 | 0.00703079 | missense | ARMC4 | GRCh38.p7 | 10:27860723 | GCACGTTGGTGTCAT[C/G/T]TGATTTCAGATAACG | 55130 |
| rs145581727 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27945275 | ATGTACACAGAGCTA[A/G]GAGATGGTTCCCCCA | 55130 |
| rs145616204 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ARMC4 | GRCh38.p7 | 10:27971490 | TGTTGGAGTTAGGTG[A/G]ACAGTAACGTGATGT | 55130 |
| rs145619075 | snp | A/C | 0.00398149 | 0.0444398 | missense | ARMC4 | GRCh38.p7 | 10:27935163 | TCTTGGCAGCATTCT[A/C]CCAAGGCCCCAACCA | 55130 |
| rs145644135 | snp | A/C | 0.00517822 | 0.0506191 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:28000450 | GCATCACACCTGTGG[A/C]GGTAATGCAGGTCAC | 55130 |
| rs145647909 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARMC4 | GRCh38.p7 | 10:27910624 | TAGCCAGGCATGGTG[A/G]TGCACGACTCTAATC | 55130 |
| rs145648104 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | ARMC4 | GRCh38.p7 | 10:27976328 | TAAGAAAATGATCTT[C/T]ACTCACTAACAATAT | 55130 |
| rs145691388 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27918573 | GATAAAACATCTACA[A/G]AAACCTACCACTAAC | 55130 |
| rs145691866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27856204 | GCTGATACATTTGAA[A/G]AGGAAGTCTGTGCAA | 55130 |
| rs145703923 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | ARMC4 | GRCh38.p7 | 10:27922482 | GAATGTTATATATAA[A/C]AAAACAGAAATAATG | 55130 |
| rs145716991 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27815139 | CGTCTTAGCAGATCT[A/T]TTTATCCTACCTTCC | 55130 |
| rs145723361 | in-del | -/CTGA | 0.0659589 | 0.169201 | intron-variant | ARMC4 | GRCh38.p7 | 10:27928726 | TACATACTATGCAAT[-/CTGA]CTTTCATTTTCTAGT | 55130 |
| rs145735744 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27879753 | TTCCCAACTTGGTAG[A/G]TAAGAGTCTACTAAC | 55130 |
| rs145742175 | snp | A/C/T | 8.26407e-05 | 0.00642765 | missense, stop-gained, intron-variant | ARMC4 | GRCh38.p7 | 10:27944296 | CATTCGCGATAGTCT[A/C/T]GGCTGCCAAACATTT | 55130 |
| rs145790274 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27857661 | TAGAAACTGAACTCA[C/T]TATATTTCAGACCCT | 55130 |
| rs145791638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27831578 | TAAGCAACTTGCCCA[A/G]AGTTGCAGATCTTGG | 55130 |
| rs145859863 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARMC4 | GRCh38.p7 | 10:27951057 | TATGACTAAATCTCA[C/T]AGGAAATGTTTTAGA | 55130 |
| rs145888160 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27825433 | GATCTGGGAGGATGG[A/T]AGCCTCCTTTAGAAA | 55130 |
| rs145909993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27939444 | ATGCAGGCCGGGCAC[A/G]GTGGCTTATGCCTGT | 55130 |
| rs145919015 | snp | A/T | | | stop-lost, synonymous-codon, intron-variant | ARMC4 | GRCh38.p7 | 10:27812514 | GTCCATTTAAATTTC[A/T]AGTGTATCTTGCCTT | 55130 |
| rs145941046 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27854176 | GAAATCATAAGATAC[A/C]ATGACATACCTGTTA | 55130 |
| rs145961853 | in-del | -/GAAA | 0.00993419 | 0.0697739 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27959255 | GGAGGAAGAAAGAAG[-/GAAA]GAAAGAAAGAAAGGA | 55130 |
| rs145982996 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27832849 | CTTTTTCAGCATATC[A/G]TTTTACTGTGACCTA | 55130 |
| rs145989518 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27989886 | TTGAAAAATAAAAAA[C/T]GCCAGCTATGGACAA | 55130 |
| rs146005810 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27889762 | AGTAGAACAGTCTCA[C/T]GGTTAAGCAGCCCCG | 55130 |
| rs146007770 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ARMC4 | GRCh38.p7 | 10:27952339 | AAAAGACTACACATC[A/G]ATGAGAATTTACAAC | 55130 |
| rs146010295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27995403 | CGGTATTTGCCCTGA[A/G]ATTAATAACTTCTTT | 55130 |
| rs146030021 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27955311 | TACTGAGTTCCTTTA[C/T]GGCAAGGGTTCCCTG | 55130 |
| rs146041171 | snp | A/C | 3.30087e-05 | 0.00406242 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27987417 | GGCTTCCTTCAACTT[A/C]CCAGTTTTGGCAATA | 55130 |
| rs146060758 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ARMC4 | GRCh38.p7 | 10:27837343 | TTTTTGTTTTTACTT[C/T]TCTGTATGCAAAATG | 55130 |
| rs146111054 | snp | A/C | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27904005 | TTCTCCAAATAAGGA[A/C]TACCTGTTGCCAAAA | 55130 |
| rs146127402 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27869896 | TTCCAACAGTGATGT[C/T]TGATGATGTGGGGAA | 55130 |
| rs146141085 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27850951 | TGGAAGTCTGGGAGA[A/C]CCACAGCCACTAGAG | 55130 |
| rs146148608 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27875123 | TCTTCAATCACTGAT[A/G]CCCTTTCTTCCAGTT | 55130 |
| rs146150537 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27941015 | TTGGGAGCTTATACA[A/T]TTCCTTCCCACAAGA | 55130 |
| rs146169523 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | ARMC4 | GRCh38.p7 | 10:27889271 | GGGATAAGGAAGATT[C/T]CACACTCGGGGTAGT | 55130 |
| rs146183027 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | ARMC4 | GRCh38.p7 | 10:27819672 | TCTGAGAGGCTGAGA[C/T]GGGAGGATGGCTTGA | 55130 |
| rs146187246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27893729 | GACAGGGGCAGTGAC[A/G]GGGAGAAAGAAAGGG | 55130 |
| rs146233674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27955994 | GATCCACCAGGCATC[C/T]GGTGGCCTGAGAATA | 55130 |
| rs146250408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27850955 | AGTCTGGGAGAACCA[C/T]AGCCACTAGAGTCTT | 55130 |
| rs146251505 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARMC4 | GRCh38.p7 | 10:27916600 | CCTCAGCCTGTTCAA[C/T]GTGAAGATGACCAAG | 55130 |
| rs146270293 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27921154 | CTTACAAAATATTAA[C/T]AGAAATACCTGTTCC | 55130 |
| rs146309511 | snp | C/T | 8.23961e-05 | 0.00641804 | missense | ARMC4 | GRCh38.p7 | 10:27860702 | AGGCCTGAGCTGTCG[C/T]CCGATGCACGTTGGT | 55130 |
| rs146370272 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27903362 | TGAATGGGCAAAAGC[A/T]GTAAGCATTCCCTTT | 55130 |
| rs146393537 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27969526 | GTTAAAAAAGTTGCC[C/T]ATGCATTTTTCATTT | 55130 |
| rs146400187 | snp | C/T | 0.143959 | 0.226396 | intron-variant | ARMC4 | GRCh38.p7 | 10:27849400 | CATACCGGGGCCTGT[C/T]GTGGGGTGGGAGGAG | 55130 |
| rs146433482 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27932765 | CCAGTCACTCTTTCA[A/T]TCACACTGTTTTCTT | 55130 |
| rs146452449 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27899445 | TACCCCAGTGGTGCC[C/T]GGAATGCCAGCGAGA | 55130 |
| rs146452990 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ARMC4 | GRCh38.p7 | 10:27826342 | ATTGCAGCAATGGCA[C/T]ACACATTATGATCTC | 55130 |
| rs146476576 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | ARMC4 | GRCh38.p7 | 10:27948261 | GATTTTTTTTTAGAA[C/T]AGTTTTATATTAGGG | 55130 |
| rs146489459 | snp | A/C | 5.17433e-05 | 0.00508616 | synonymous-codon, intron-variant | ARMC4 | GRCh38.p7 | 10:27944249 | ACCCCCGTGCTGCCT[A/C]ACCACCCGCCGTGCT | 55130 |
| rs146490585 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27844960 | AGTCTATTAGCTCAG[C/T]CCCTTCTAGGCACAT | 55130 |
| rs146515267 | in-del | -/AA | 0.390477 | 0.2068 | intron-variant | ARMC4 | GRCh38.p7 | 10:27890772 | GGTATATATATATTT[-/AA]AAAAAAAAAAAACTT | 55130 |
| rs146568420 | snp | C/T | 0.000266934 | 0.0115497 | synonymous-codon, intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27971290 | ATCCTTTTCCTTTTG[C/T]TGGTCTTCACTGAAG | 55130 |
| rs146576050 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ARMC4 | GRCh38.p7 | 10:27879994 | TTCCAGATGTGGTCC[A/G]ACAAGAGCAGAGTGT | 55130 |
| rs146578016 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27945875 | AGCAAGAAGGCTGTT[C/G]ATTTTTGTAAAAGGT | 55130 |
| rs146578096 | snp | C/T | 0.000556961 | 0.0166784 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984978 | TCAGTGGTGCAATCT[C/T]GGCTCAATACAATAG | 55130 |
| rs146592560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27867285 | CAGCAGCAGAAGCAG[C/T]TGCGAATGGACTTTT | 55130 |
| rs146596035 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27931984 | ATAGCTTAGACTAGC[C/T]CACCTTAAATACACT | 55130 |
| rs146610504 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27826074 | ATACCCGGACCTTAG[C/T]AATACCAGTGACTGC | 55130 |
| rs146630922 | in-del | -/AC/ACAC | 0.089084 | 0.191327 | intron-variant | ARMC4 | GRCh38.p7 | 10:27827365 | AGCAGACACACACAT[-/AC/ACAC]ACACACACACACACT | 55130 |
| rs146689340 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | ARMC4 | GRCh38.p7 | 10:27987616 | TAAATTTAAGACATT[C/T]AGACAGATTATTCCT | 55130 |
| rs146691598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27861983 | CTGCTTATTCTGTCT[A/G]GCACAGCTCTGGATA | 55130 |
| rs146696558 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27928479 | CCTTCAATGATCCTC[A/G]ACTGACCTCAAAACA | 55130 |
| rs146714682 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27848217 | TGGTACTGGTACCAA[A/T]ACAGAGATATAGACA | 55130 |
| rs146716317 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | ARMC4 | GRCh38.p7 | 10:27913790 | ACAAGAAGATACTAT[C/T]TCACATGAGTCGGAA | 55130 |
| rs146727482 | snp | A/C | 1.64904e-05 | 0.00287139 | missense | ARMC4 | GRCh38.p7 | 10:27995087 | GTGATTTCGAGGATT[A/C]CAGTTCCATGTCCGG | 55130 |
| rs146752098 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27814024 | GCAATTCCAGATGGA[A/T]TAATGATGTTGTAGG | 55130 |
| rs146752110 | in-del | -/A | 0.0667028 | 0.170006 | intron-variant | ARMC4 | GRCh38.p7 | 10:27943376 | GTTTATTTCTAGTGG[-/A]TTTTTTTTAAAGATG | 55130 |
| rs146777204 | in-del | -/GAAA | 0.127254 | 0.217792 | intron-variant | ARMC4 | GRCh38.p7 | 10:27892069 | TTGATCGTTCAGCTT[-/GAAA]GAAACAGTTTTACAC | 55130 |
| rs146799446 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27949151 | AACAGGAAGTGAGCT[A/G]CCTCAAATCACTTTT | 55130 |
| rs146815853 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27886565 | TAACTTGAAGCCATA[C/G]AAAAATATAAAGTTC | 55130 |
| rs146816821 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARMC4 | GRCh38.p7 | 10:27952500 | CTATCAACCCATCAC[C/T]TAGATTTTCAGCCCC | 55130 |
| rs146817700 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27910204 | TTAGAATTTCTGCAA[C/T]AGCTCCTTGAGATCA | 55130 |
| rs146818276 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27950384 | TTTATTTGCAAATCT[A/C]TTTTACACTGATGAC | 55130 |
| rs146834528 | snp | A/C | 0.0437281 | 0.141251 | intron-variant | ARMC4 | GRCh38.p7 | 10:27901470 | ACATAATAATATTAA[A/C]CTTAAATGTAAATGG | 55130 |
| rs146898926 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ARMC4 | GRCh38.p7 | 10:27891932 | TCTGCAGCAGACAGT[C/T]TTGCTTCTTAAGAAC | 55130 |
| rs146984777 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27868156 | TGCCAGTGAGAATGA[C/T]GATCATTAAAAAGTC | 55130 |
| rs146990009 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27933941 | TAGGATTTTGCTGTG[A/T]CCCCACCCAAATCTT | 55130 |
| rs147001136 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27827924 | GACTATATATTACTT[C/G]TGCTACTTTAAAAGT | 55130 |
| rs147018026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27832058 | CTTTCATCTTTGTAT[C/T]TTCAGGGGCTAACAC | 55130 |
| rs147092268 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | ARMC4 | GRCh38.p7 | 10:27957481 | TAAGACAGACAACCT[A/G]AACCATCAGGATAGC | 55130 |
| rs147105160 | snp | A/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, intron-variant | ARMC4 | GRCh38.p7 | 10:27812226 | AAAGCATCACTGAAC[A/T]AAAAATACATCATAT | 55130 |
| rs147105177 | snp | A/G | 0.00768234 | 0.0614992 | intron-variant, synonymous-codon | ARMC4 | GRCh38.p7 | 10:27853292 | GAATCGCTTGAATCC[A/G]GGAGGTGGAGGTTGC | 55130 |
| rs147107821 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | ARMC4 | GRCh38.p7 | 10:27918853 | CCAGCATACATAAAG[G/T]TATATTTGAATATAC | 55130 |
| rs147121116 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | ARMC4 | GRCh38.p7 | 10:27815704 | CTTCCCCCAAACAAA[A/T]ATTGTTAGAGTTCAT | 55130 |
| rs147124402 | snp | A/G | 0.0001487 | 0.00862137 | synonymous-codon, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983897 | CAGAGTCTCACCATC[A/G]TGAGGTTTCACCAGC | 55130 |
| rs147131680 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944731 | CAAGAACCAGGCAAC[A/G]AGGCATGGCAGAAAC | 55130 |
| rs147147096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27947853 | CCATCCTAACATTCT[C/T]AATCGCTCGTGCTGA | 55130 |
| rs147160225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27843972 | TGGGAAGCTGAGGTC[A/G]GAGGATTGCTTGAGG | 55130 |
| rs147163770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27908535 | AACTTAATAACCTTT[A/G]CAAACATGGCTTTGT | 55130 |
| rs147175768 | snp | A/C | 0.137811 | 0.223414 | missense, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27961681 | TTTCTGAGGAGCTAT[A/C]GCTAACAGTTTCCTC | 55130 |
| rs147236969 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27927786 | TCTTTACAGAGACTT[C/T]TTCTTCATTCTCCTT | 55130 |
| rs147238676 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27996119 | CACGTTCTGACTTCA[C/T]AATGAACATTTAATG | 55130 |
| rs147253535 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ARMC4 | GRCh38.p7 | 10:27930670 | CAAACAAAAACTTTA[C/T]ATAATTTTTTGATTC | 55130 |
| rs147253742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27998131 | CCGAATTCTTTAGGG[A/G]GCTACGGAAAGGCAG | 55130 |
| rs147269040 | snp | A/C/T | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27825289 | GCCAAGTTCTCAATA[A/C/T]GCAAAAAGATCTGGA | 55130 |
| rs147285367 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | ARMC4 | GRCh38.p7 | 10:27828933 | GTATAAGTTCCTAAT[A/G]TTATGTTTGCCTTTA | 55130 |
| rs147333449 | in-del | -/TT | 0.491783 | 0.0635686 | utr-variant-3-prime, intron-variant | ARMC4 | GRCh38.p7 | 10:27812185 | GGGAAGGCCATATCC[-/TT]TTTATTAAAATCGCC | 55130 |
| rs147345414 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27973876 | TGTTTTCCACAATGA[C/T]TGAACTAATTTACAC | 55130 |
| rs147357353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27912459 | GCTACGTTTCTCAGG[C/T]TCTTGTTATGTTAAC | 55130 |
| rs147361608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27977639 | AATATTTATATTTCA[C/T]GTATCTAACAGAATA | 55130 |
| rs147373967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27877425 | ACAGGGTCCCATAAG[C/T]TTCCTAATGACTCCT | 55130 |
| rs147390148 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27881662 | TGAAAAGAATGAGCC[A/G]GCAAAAATACATCCT | 55130 |
| rs147433407 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27909651 | GGCTAAATCCTGTCT[C/T]TACTAAATATACAAA | 55130 |
| rs147480495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27926942 | TTACAAAACAAGAAA[C/T]GAAAATTCAGCACAC | 55130 |
| rs147494145 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27864305 | CTTGGTTTGGTTTTC[C/T]TGGGGTGGCATATGA | 55130 |
| rs147497080 | snp | C/T | 0.000150109 | 0.00866209 | synonymous-codon, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27961607 | AATTTGCCAATATTC[C/T]GATGGCAAATCTGCA | 55130 |
| rs147550795 | in-del | -/A | 0.141596 | 0.225274 | intron-variant | ARMC4 | GRCh38.p7 | 10:27921312 | ACGAAAAAAAAAAAG[-/A]AAAAAAAAAGAACAT | 55130 |
| rs147552403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27835546 | TCAAAAACCCACATA[C/T]AACTTTTGACTGCCC | 55130 |
| rs147553676 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27903841 | TGTCACAGGCTGCCT[C/G]TCATTTCCATGAGTT | 55130 |
| rs147564767 | snp | A/G | 1.64814e-05 | 0.00287061 | missense | ARMC4 | GRCh38.p7 | 10:27860773 | TTGTGCTCACCGAAG[A/G]CCACTCTATTCCTGC | 55130 |
| rs147570115 | snp | A/G | 0.0722614 | 0.17581 | intron-variant | ARMC4 | GRCh38.p7 | 10:27906765 | AACTAATACAGGAAC[A/G]AAAAACCAAACACCG | 55130 |
| rs147592957 | in-del | -/AATTT | 0.461703 | 0.132974 | intron-variant | ARMC4 | GRCh38.p7 | 10:27891952 | TTCTTAAGAACAAAG[-/AATTT]AATATATGGACTTTT | 55130 |
| rs147609314 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27970372 | TGACAGTTTCGCTGA[C/T]TAGCTCCATATAATT | 55130 |
| rs147642259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27942133 | AGTGCTCAGAAAGCC[C/T]GTAGCATTTGTGACT | 55130 |
| rs147656241 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | ARMC4 | GRCh38.p7 | 10:27891111 | CCTGATTGGGCATGG[A/C]CCGTTGGGCAGCTGA | 55130 |
| rs147657340 | snp | A/C/T | 0.00438332 | 0.0466095 | intron-variant | ARMC4 | GRCh38.p7 | 10:27818107 | ATAATTGAATGTGAG[A/C/T]GCTGCCAGCCTGGAT | 55130 |
| rs147673210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27821334 | CATTGCTTTGTTATA[C/T]ACCCAGAGGGGCTAG | 55130 |
| rs147675539 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27895270 | CACCAAAACGATAGC[A/C]GCTAACTACATGTAA | 55130 |
| rs147712943 | in-del | -/T | 0.106278 | 0.204558 | intron-variant | ARMC4 | GRCh38.p7 | 10:27891664 | ATATAGTTGAACATC[-/T]TTTTTTTCTTAATAA | 55130 |
| rs147732197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27987007 | CCTTGGCAGTATGCC[A/G]AGAGAGAGTGGATTC | 55130 |
| rs147748243 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | ARMC4 | GRCh38.p7 | 10:27991349 | AGGAAAAGACCATCA[C/T]GTAACATGAACAGGG | 55130 |
| rs147754381 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ARMC4 | GRCh38.p7 | 10:27876436 | ACCCAGGCAAACAGC[A/G]TCTGGAGTGGACCTC | 55130 |
| rs147760622 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ARMC4 | GRCh38.p7 | 10:27871352 | CGTGCAGAAGCTCTT[C/T]AGTTTAATTAGATCC | 55130 |
| rs147760669 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27909271 | GCTGGACAGAAATAA[C/G]TTGTCATTGCAGTGG | 55130 |
| rs147776910 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | ARMC4 | GRCh38.p7 | 10:27875554 | ATGTCCTTTCTGTTT[G/T]TTAGTTTTGGTGGTT | 55130 |
| rs147832934 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27904314 | GATGCTGTGTATGCG[C/T]GGGGAACATGGCGTC | 55130 |
| rs147863894 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27853043 | ACTTCCCCTCCCAAT[A/G]AAGGCAGAGGTTGTA | 55130 |
| rs147880687 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27855734 | TACATGTACTGAGCC[C/T]AGGAGGCAGCTAGCC | 55130 |
| rs147940376 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | ARMC4 | GRCh38.p7 | 10:27953290 | AAATGAAATTTTATA[C/G]CCATTGAACAATTAC | 55130 |
| rs147957129 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | ARMC4 | GRCh38.p7 | 10:27957329 | GAACAGCAAAGCCCT[C/G]CCACTAAGGAACCTC | 55130 |
| rs148005347 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27853967 | AAGACTAGCTACAGA[C/T]GGGGAGAAAATATTT | 55130 |
| rs148010554 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27920021 | GAAACAAAACTAAGC[C/T]ATAGTTTATAGGGAT | 55130 |
| rs148018745 | in-del | -/AC | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27979445 | CACACACACACCCAT[-/AC]ACACACACACACACA | 55130 |
| rs148045262 | snp | A/T | 0.029116 | 0.117091 | intron-variant | ARMC4 | GRCh38.p7 | 10:27899966 | CACTCAAGCTCTGCT[A/T]AGGGACAGACTGCCT | 55130 |
| rs148079636 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ARMC4 | GRCh38.p7 | 10:27910791 | AAACAAACAAAAAAA[C/T]AGATACAGTCAATTC | 55130 |
| rs148093755 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27833639 | TGTGTGGGACAAAAA[A/C]TTGGGGAAAATAGTT | 55130 |
| rs148097373 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ARMC4 | GRCh38.p7 | 10:27902695 | ATAAACTAGAAAATC[A/G]AGAAGAAATGGATAA | 55130 |
| rs148111778 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27840398 | CTTTCGTGCACATCT[-/T]TTTGGAGTGCCTTCC | 55130 |
| rs148127355 | snp | C/G | 0.128288 | 0.218372 | intron-variant | ARMC4 | GRCh38.p7 | 10:27902589 | GAGAAGAATCAAATA[C/G]ACACAATAAAAAATG | 55130 |
| rs148136308 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27943961 | ATGCATTCCTAACAA[C/T]GTACAATAGGTGGTG | 55130 |
| rs148170208 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27949864 | CCATAAAGAAACGTT[C/T]GAAAGGTTTTTATCA | 55130 |
| rs148205943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27993163 | CTGGTGATCTGCCCA[C/T]CTCGGCCTTTCAAAA | 55130 |
| rs148255290 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, splice-donor-variant | ARMC4 | GRCh38.p7 | 10:27835980 | AATACATTTACTATA[C/T]ATTAAGTGGAAGTGG | 55130 |
| rs148256668 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ARMC4 | GRCh38.p7 | 10:27929771 | GTCATTAAAAGAAGA[C/T]GCAGAGAAGTTTACA | 55130 |
| rs148270170 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | ARMC4 | GRCh38.p7 | 10:27824374 | GAACGGATTAATGCT[C/G]TTACAGGGGGGTTGG | 55130 |
| rs148273306 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27897020 | CGCCTAATTCCTGTA[A/C]TTAATGTACTCTTTT | 55130 |
| rs148286065 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | ARMC4 | GRCh38.p7 | 10:27811799 | TTCAAGAAAATGTTG[C/G]TAAATCTCTGTGAGA | 55130 |
| rs148286126 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27895263 | ACCTGGGCACCAAAA[C/T]GATAGCCGCTAACTA | 55130 |
| rs148289983 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27881037 | TCAGCAATGTGGCTT[C/T]CAGCAAACTACTTAA | 55130 |
| rs148295264 | snp | A/G | 0.00353766 | 0.0419084 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27860664 | GGTGATGCAGTTATC[A/G]GCGTCTTCTGAGAGT | 55130 |
| rs148299600 | snp | A/C | 1.65255e-05 | 0.00287445 | missense, utr-variant-5-prime, intron-variant | ARMC4 | GRCh38.p7 | 10:27981539 | TTTTTATAAATTGAA[A/C]CTTTTCTCTCATAAT | 55130 |
| rs148311329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27935355 | CCAATGATACAGATA[C/T]TATTAAATCCCCATT | 55130 |
| rs148338816 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27816494 | TTGAACAGCCATATG[C/G]TCTGTGCTGGGCTGG | 55130 |
| rs148346788 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27972698 | GAGCACACATACTAA[C/T]AGAGGATCAATTAGC | 55130 |
| rs148365160 | in-del | -/AGG | 0.0322114 | 0.122752 | intron-variant | ARMC4 | GRCh38.p7 | 10:27878092 | GAACCTTCACTACTT[-/AGG]AGATTAGTAATTTTA | 55130 |
| rs148377147 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27914190 | ATATTAAGTGAGAGC[A/C]AATTATATCCCATGC | 55130 |
| rs148396549 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27912803 | AAACCAAGTTGGCAA[A/T]TCAGTAAAATGGGAA | 55130 |
| rs148416058 | snp | C/T | 6.4406e-05 | 0.0056744 | missense | ARMC4 | GRCh38.p7 | 10:27985149 | GAATATTTAATGCAA[C/T]TGAGTTTTCTTTCAT | 55130 |
| rs148445025 | in-del | -/GAAA | 0.0437281 | 0.141251 | intron-variant | ARMC4 | GRCh38.p7 | 10:27842702 | AAATTTAAATATGCT[-/GAAA]GAAAAAGTCAAGTCA | 55130 |
| rs148483256 | in-del | -/CCTTATATGAA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27963623 | AACTTGTTGCTAAGG[-/CCTTATATGAA]CCTTATATGAACCAA | 55130 |
| rs148523965 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27995949 | TCTTTCAGCCTTTTT[A/G]TCTAAATTAGTTATC | 55130 |
| rs148540495 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27956011 | GTGGCCTGAGAATAC[A/G]CAATTTGTGGTTACA | 55130 |
| rs148552356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27877039 | TGTCTATCACTCAGT[A/G]AACATTCAAAAATAT | 55130 |
| rs148567543 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27838255 | GAAATACCATTATTA[G/T]TAGTAGTAATTCTTA | 55130 |
| rs148574011 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27931448 | TACTGCCTTCTCATC[A/G]TCTACTTTACTATTT | 55130 |
| rs148586111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27825498 | ATACTGAACTCAGAA[A/G]TTGCTGGAATTGCTG | 55130 |
| rs148589903 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | ARMC4 | GRCh38.p7 | 10:27898756 | ATGTATTGATATTGA[C/T]GAATACATTGCCAAA | 55130 |
| rs148605072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27813845 | AAGGGTACTGTATTA[C/T]TTCATGTAGAGGTGA | 55130 |
| rs148606603 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | ARMC4 | GRCh38.p7 | 10:27882225 | AAAGAAAGAAAGAAA[G/T]AAAGAAAGAAATATG | 55130 |
| rs148613172 | in-del | -/ATGT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27940259 | ATATAAATGTCAGTA[-/ATGT]TATGTGATATATATA | 55130 |
| rs148625218 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | ARMC4 | GRCh38.p7 | 10:27937399 | GTGGAGTGCAGTGGC[A/G]TGATCTCGACTCACT | 55130 |
| rs148655241 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27817668 | CAAAAGACATGATTC[A/C]TTCTTTTTTATGACT | 55130 |
| rs148695561 | snp | A/G | 0.021333 | 0.101051 | intron-variant | ARMC4 | GRCh38.p7 | 10:27916155 | TGGGGACAGAGACTG[A/G]AAAGTGTGAAAGAAA | 55130 |
| rs148695637 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983309 | ACTGGGCAGTGCCCA[C/T]TCTTCAGAGATCTGG | 55130 |
| rs148741849 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ARMC4 | GRCh38.p7 | 10:27829953 | AAAAAAATGTAAGCA[A/G]TGGAACCCATTTCTT | 55130 |
| rs148747825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27921558 | TCTTGGAGTTTGCTG[A/G]GATTCCTGACAACTC | 55130 |
| rs148764188 | snp | A/G | 0.000345978 | 0.013148 | missense, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27936760 | TGATGGAACATTTCC[A/G]TATAGCCCCTGTGAC | 55130 |
| rs148764990 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27908501 | TTGGGTACTCACAGC[A/G]GAGAAGAAGGCCAAA | 55130 |
| rs148838721 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ARMC4 | GRCh38.p7 | 10:27903805 | ATACATGCAAGAAAC[C/T]CTTCTCCTCTGAAAA | 55130 |
| rs148841404 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997132 | TCATGAAATAAAGTG[C/T]AGAAATTAGTGCACA | 55130 |
| rs148855743 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27867450 | AGAAACTACACGGAA[C/T]AGCATCATCCAAATT | 55130 |
| rs148896287 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:28000869 | ATGAAACACTACCTG[A/G]GCCCAGTCACTCCCT | 55130 |
| rs148908705 | snp | C/T | 0.00013183 | 0.00811775 | missense | ARMC4 | GRCh38.p7 | 10:27940633 | GAAGTCTTCAGCAGC[C/T]GAGCCAACAGAGGAA | 55130 |
| rs148924529 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | ARMC4 | GRCh38.p7 | 10:27885400 | CTGTAATCCCAGCTA[C/T]GTGGGAGGCTGAGGC | 55130 |
| rs148930400 | snp | C/T | 0.00176581 | 0.0296612 | missense, intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27971255 | GCTGCTTCTTCCTTC[C/T]TGGGGGCTTTGCCAA | 55130 |
| rs148957601 | in-del | -/TA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27946010 | CCATTATCTATTGTG[-/TA]TATATATATATAATT | 55130 |
| rs148971171 | snp | C/T | 0.138207 | 0.223612 | intron-variant | ARMC4 | GRCh38.p7 | 10:27873909 | CAATTCCTGGATATC[C/T]TTGTTAACTTTCTGT | 55130 |
| rs148977753 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27818722 | CTCTCATGGCCACCC[A/G]CCTCGCTTCTGCTCC | 55130 |
| rs148979137 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27892384 | AAAAAGACCGTGCGG[C/T]TTTCTAAGTGAAGAT | 55130 |
| rs149016350 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27986598 | AAGTAAAAAAAAGAC[C/G]ATCTTCCCATCTCAC | 55130 |
| rs149042698 | snp | A/G | 0.127944 | 0.218179 | intron-variant | ARMC4 | GRCh38.p7 | 10:27901550 | AAGACCCACCGGTGT[A/G]CTGTATTCAGGAGAC | 55130 |
| rs149045218 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | ARMC4 | GRCh38.p7 | 10:27871022 | CCAGCATCTGTTGTT[G/T]CCTGACTTTTTAATG | 55130 |
| rs149060296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27831584 | ACTTGCCCAAAGTTG[C/T]AGATCTTGGCAAAGT | 55130 |
| rs149067543 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27924012 | AGAAAGAAAGAAAGA[A/G]AGAAAGAAAGAAGGA | 55130 |
| rs149067969 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27992491 | GCCAAAAGTACAAGA[C/T]CAGTCAGAGCAACAT | 55130 |
| rs149081016 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27909857 | AGACTCAGAACACTA[C/T]GGAATGATAACTTCC | 55130 |
| rs149085339 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27975020 | GAATGGGATTGCATT[C/G]CTGATTTGGCTCTTG | 55130 |
| rs149129409 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27821477 | TTTTCATTTTCCTAC[A/G]AGCCTCACAAGCAAA | 55130 |
| rs149136135 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27914063 | AAAATTCACAGTAGC[A/G]AAGACATAAAATCAA | 55130 |
| rs149168196 | snp | A/G | 5.17174e-05 | 0.00508488 | splice-donor-variant, intron-variant | ARMC4 | GRCh38.p7 | 10:27981464 | GAAACCATAAAACTT[A/G]CCAATTTAGACATAT | 55130 |
| rs149185826 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | ARMC4 | GRCh38.p7 | 10:27853827 | AAGCATGAAATCCTT[A/G]AGACCATGTGTTAGG | 55130 |
| rs149226430 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27952959 | TCTCAAACTGTAGTG[A/T]GCATATATTGTTTTT | 55130 |
| rs149244451 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27888495 | GTCTATTCATGTTCT[C/T]TGCCCTCTTTTTAAT | 55130 |
| rs149245065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27951380 | CTGTAGTAATTAAAA[C/T]AGCATGTAACTAGCA | 55130 |
| rs149274011 | snp | A/T | 9.91359e-05 | 0.00703975 | splice-acceptor-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984292 | TTAAACTTATTTCTC[A/T]GAAATAAATGTTTAA | 55130 |
| rs149330246 | snp | G/T | 0.0244538 | 0.107838 | intron-variant | ARMC4 | GRCh38.p7 | 10:27827199 | TTTCCAGGAATCCCT[G/T]TCTTAACCCATTATG | 55130 |
| rs149334242 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | ARMC4 | GRCh38.p7 | 10:27989369 | AAATGAATGAATAAA[A/C]TATTTCTAGACTTGC | 55130 |
| rs149355330 | in-del | -/AC | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27832537 | CACACACACACACAG[-/AC]ACACACACACACACA | 55130 |
| rs149368374 | snp | A/C | 5.04333e-05 | 0.00502137 | splice-donor-variant, missense | ARMC4 | GRCh38.p7 | 10:27939896 | GGAGAGTTCACTGCA[A/C]CTGGTAAATGGCCAT | 55130 |
| rs149380558 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ARMC4 | GRCh38.p7 | 10:27832887 | ACTGAGAAAATTATC[C/T]GACTTATCATGAAAA | 55130 |
| rs149385684 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27926459 | ACTTACAAATTAACC[A/G]GACAAAAATAAACAA | 55130 |
| rs149389889 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27995654 | ACTTTCTTACAGTGA[C/T]AATATCTGCATCATC | 55130 |
| rs149402765 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27911472 | ATGGACCATTGGGAA[A/T]CTACAGTCTTGTGAG | 55130 |
| rs149432727 | snp | A/G | 0.00176858 | 0.0296844 | synonymous-codon, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27961601 | CTTCTGAATTTGCCA[A/G]TATTCTGATGGCAAA | 55130 |
| rs149451747 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27823574 | GATTAAATGGGAAAC[A/G]TAATGTAAAGTGCTC | 55130 |
| rs149459051 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27915445 | GCTCTCCGGGGACTC[C/T]TTTAAAAGGGCATTA | 55130 |
| rs149473503 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27813364 | GCAGTTTACTCAAAT[A/G]TCTGTTGCTACACGT | 55130 |
| rs149540369 | snp | A/C | 0.0275645 | 0.114116 | intron-variant | ARMC4 | GRCh38.p7 | 10:27863264 | AGGCAGCACCTCAGC[A/C]CCACATCTGGGGGCC | 55130 |
| rs149577425 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27904936 | TTGCTATTATACATG[A/G]GTTTTTCTTAAGTCC | 55130 |
| rs149616301 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27946782 | GTACACATATGCAAA[A/C]CCTCTTGTGAATTCA | 55130 |
| rs149631728 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ARMC4 | GRCh38.p7 | 10:27908473 | CAGGAGCATAACCTC[A/G]CAGTAAGGTCCATTG | 55130 |
| rs149687455 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27941725 | CAGACCTCCCTAGAG[C/G]TGCAATTGGCTGTCA | 55130 |
| rs149687959 | snp | C/T | 6.59239e-05 | 0.00574087 | missense | ARMC4 | GRCh38.p7 | 10:27860713 | GTCGCCCGATGCACG[C/T]TGGTGTCATTTGATT | 55130 |
| rs149694203 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27967378 | CCACTGACAAAGTAA[C/T]GAAGGACTCCCCCGT | 55130 |
| rs149702286 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27835054 | GCGGCACAGCACATC[C/T]GTACTTGTAGACATC | 55130 |
| rs149704360 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27903484 | GCAATAAAGAGTATT[C/G]AAATAGGAAGAGAGG | 55130 |
| rs149705511 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARMC4 | GRCh38.p7 | 10:27928478 | ACCTTCAATGATCCT[C/T]GACTGACCTCAAAAC | 55130 |
| rs149738625 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | ARMC4 | GRCh38.p7 | 10:27878396 | ACTGGGTGTTTTGGC[A/G]TAAAGCAATTAAATT | 55130 |
| rs149771584 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27825330 | AAGGTGCAGCCTAGC[A/G]AAAACAAAAATGCTC | 55130 |
| rs149774081 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ARMC4 | GRCh38.p7 | 10:27917973 | TGACCCAAGAAGGAA[C/T]TGAAAATCTACATAG | 55130 |
| rs149777950 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ARMC4 | GRCh38.p7 | 10:27986109 | GTGGTCATGGGATAT[A/G]CCAAGGCCTTAAGGC | 55130 |
| rs149790717 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27884778 | CTGGGGTGAGCCTCT[C/T]TGGAAAATTAAGGCA | 55130 |
| rs149861607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27866674 | GTGAAAGGAAGTAGG[C/T]ATCACATGGTAAAAG | 55130 |
| rs149862624 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27931244 | ATATTACATATGGGT[C/T]AATAATTCATAGCAT | 55130 |
| rs149928087 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ARMC4 | GRCh38.p7 | 10:27854841 | ACTCAGAGATAAAAG[A/G]GTTGATTGAGCCACA | 55130 |
| rs149933423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27948156 | GACAATTTACAGTTA[C/T]CATCAAGAAGTTAGA | 55130 |
| rs149944421 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARMC4 | GRCh38.p7 | 10:27817383 | TTCGAGGGTACAAGT[A/G]CAAATTTCTTACATG | 55130 |
| rs149949342 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | ARMC4 | GRCh38.p7 | 10:27909600 | AGGCAGGCAGATCAC[A/T]TGAGGTCAGGAGTTC | 55130 |
| rs149949970 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | ARMC4 | GRCh38.p7 | 10:27844809 | TCTTTTTCATTTCTT[A/C]TCACTTGTAGCTCTA | 55130 |
| rs149958990 | snp | G/T | 1.64936e-05 | 0.00287168 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27971142 | TCTTCCAGTTTAAGC[G/T]TGGTTCCCATCTCTT | 55130 |
| rs149971830 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | ARMC4 | GRCh38.p7 | 10:27991253 | GTAGAGCTATTTGAC[C/G]CCCAGCCCCCACCCC | 55130 |
| rs149975922 | snp | C/T | 0.16846 | 0.236329 | intron-variant | ARMC4 | GRCh38.p7 | 10:27955139 | TGCCTTTCTAACTAC[C/T]GGAGTTGATTCGAGT | 55130 |
| rs149981194 | snp | C/T | 0.000659131 | 0.018142 | missense | ARMC4 | GRCh38.p7 | 10:27860663 | TGGTGATGCAGTTAT[C/T]GGCGTCTTCTGAGAG | 55130 |
| rs149983629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27890850 | GGCCAGATGGGTGCA[C/T]ACTTAGAACTATTTG | 55130 |
| rs149988136 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ARMC4 | GRCh38.p7 | 10:27952577 | GACAGGCCCTGGTGT[A/G]TGTTGTTACCCTCCC | 55130 |
| rs150023363 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27996745 | AGAGCTCAGCATTTT[A/G]GAAAATGACACCATT | 55130 |
| rs150071917 | snp | A/G | 0.0670745 | 0.170406 | intron-variant | ARMC4 | GRCh38.p7 | 10:27962745 | CTCATGCACACGCAC[A/G]CTCATCACACCAGCT | 55130 |
| rs150090074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27827005 | TCAAGGCCATTCGTA[A/G]TCGCTTTGCTATGCA | 55130 |
| rs150094265 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27920136 | GAGAGAGGTGGCACT[C/G]AGTGGGCTGTGAGGA | 55130 |
| rs150094455 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27989261 | GGGACTTTATGAGTC[C/T]GATTCTGCTGGGTGC | 55130 |
| rs150162784 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27968668 | TTAGGTCACTGCTCT[C/T]TGCATTAAATACATT | 55130 |
| rs150178780 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | ARMC4 | GRCh38.p7 | 10:27933453 | ACAACATTATCAGAT[A/G]TGCAGTTTAGGAAAG | 55130 |
| rs150179281 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27867712 | CTCAGCACTTTGGAA[A/G]GCTGAGGCAGGCGGA | 55130 |
| rs150198377 | snp | A/T | 1.64808e-05 | 0.00287057 | missense | ARMC4 | GRCh38.p7 | 10:27944836 | ATTTGACTTCATCGG[A/T]TTCAAGCAAATTTAT | 55130 |
| rs150213638 | snp | A/G | 3.30693e-05 | 0.00406615 | missense | ARMC4 | GRCh38.p7 | 10:27907772 | CCATCTAAGCGATCA[A/G]TTATCCTATCGTGGA | 55130 |
| rs150229125 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872656 | TATATGCTGGATTAC[A/G]TTTATTGATTTGCAT | 55130 |
| rs150248097 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27857314 | TTATTGTACTAATAC[A/C]TAATACATATAACAT | 55130 |
| rs150249772 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27923639 | ACATCAAACTCTACA[C/T]TCTGTTGATAAAGAA | 55130 |
| rs150267329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27911096 | CAAAAGGAACATCGC[C/T]GCCGTCCTGCACTTA | 55130 |
| rs150284436 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27964491 | CATTCACCAAACGTG[C/G]ATGGAGGGCCTGCTG | 55130 |
| rs150297564 | snp | A/G/T | 3.37862e-05 | 0.00411001 | missense | ARMC4 | GRCh38.p7 | 10:27862618 | CGAACCATTTCCCCA[A/G/T]CATCCTAGACAAAAA | 55130 |
| rs150302620 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | ARMC4 | GRCh38.p7 | 10:27955088 | GCAACACATCTACTA[A/C]CTTAAAGAATGTTTC | 55130 |
| rs150341487 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997591 | TGTAACATTTGAATC[C/T]ATTCAAATTGTATTT | 55130 |
| rs150389104 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | ARMC4 | GRCh38.p7 | 10:27901693 | CAGACTTTAAACCAA[C/T]AAAGATCAAAAAAGA | 55130 |
| rs150422508 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | ARMC4 | GRCh38.p7 | 10:27848391 | AAGCTGAAACTGGAT[C/G]CCTTCCTTACACCTT | 55130 |
| rs150441402 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27904533 | ACTGCCTCTGAGATT[G/T]GACTTGCCACTTTTA | 55130 |
| rs150441509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27836724 | GATTTCAAGGAATAC[A/G]AAAAATACACTTAAG | 55130 |
| rs150446034 | in-del | -/AAG | 0.33303 | 0.235809 | intron-variant | ARMC4 | GRCh38.p7 | 10:27922979 | AGTGAATGATTAAAT[-/AAG]AAGGAGGATGAGGAC | 55130 |
| rs150458003 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | ARMC4 | GRCh38.p7 | 10:27823064 | GGAGAATGACTTGAT[C/G]ACTGGCTGGGTCAGG | 55130 |
| rs150458651 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27895906 | TTGTTGTAGAAGGAC[A/G]CAAGGTGGGAGACAA | 55130 |
| rs150470899 | snp | A/T | 0.110167 | 0.207236 | intron-variant | ARMC4 | GRCh38.p7 | 10:27871897 | GTTCTGTGAAGAAAG[A/T]CATTGGTAGTTTCAT | 55130 |
| rs150495820 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27843173 | AATTAGAAACTGGTG[C/T]CATAGTTTATTTTTT | 55130 |
| rs150527862 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | ARMC4 | GRCh38.p7 | 10:27816941 | TTTTAGTAGAGACGG[C/G]GTTTTGCCATGTTGG | 55130 |
| rs150532459 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27887717 | AATTAAACAACACAC[G/T]TGTAAGCAACCAGTG | 55130 |
| rs150535038 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | ARMC4 | GRCh38.p7 | 10:27972756 | GCAACAGAACTTCAA[A/T]ATACATGAAGGAAAC | 55130 |
| rs150550738 | snp | A/T | 0.0314385 | 0.121371 | intron-variant | ARMC4 | GRCh38.p7 | 10:27962503 | CACATCCCTCCATAA[A/T]GCCTACACTGAAGTA | 55130 |
| rs150567841 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27859024 | TGCTATATGTCAGAC[A/G]TTTTTACCTGGCTAC | 55130 |
| rs150568089 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARMC4 | GRCh38.p7 | 10:27925511 | TACAGGTGCACACTA[C/T]CATGCTCAACTAATT | 55130 |
| rs150584677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27820000 | CAATACAAAGCAAGC[A/G]TTCCATGAATGCTAC | 55130 |
| rs150588768 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27913224 | GTACAGATTATTTTG[C/T]TACCCAGATAATAAG | 55130 |
| rs150602334 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ARMC4 | GRCh38.p7 | 10:27903033 | GTCCCTGATGAACAT[C/T]GATGCGAAAATCCTC | 55130 |
| rs150606160 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27966366 | GGAAAGCCTAAATTC[A/T]CCTTCCTTAGTCTAA | 55130 |
| rs150655393 | snp | C/T | 0.00138349 | 0.0262646 | missense | ARMC4 | GRCh38.p7 | 10:27860711 | CTGTCGCCCGATGCA[C/T]GTTGGTGTCATTTGA | 55130 |
| rs150657172 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | ARMC4 | GRCh38.p7 | 10:27906403 | TAGGAATGCTTTTAC[A/C]CTGTTGGTGGGAGTG | 55130 |
| rs150723128 | snp | A/T | 0.00776339 | 0.0618177 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27968954 | TTCCGTGTGAAACAG[A/T]TGGTCTTGGTTTTTC | 55130 |
| rs150740565 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27915232 | AAAAATGCATACGTC[G/T]TAGTCCCTTCAGGCT | 55130 |
| rs150741121 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27849603 | AGGCAAAAGCATTGC[C/G]TAGAGCTCCCCATGG | 55130 |
| rs150744353 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944488 | GTGCTATGTTTTTAA[A/G]AATTCCGAGTATACC | 55130 |
| rs150756505 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27838862 | GGATCTTTTATCAAC[A/C]AAAAAAGCTGCGGGA | 55130 |
| rs150758013 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27813236 | TTCCCATCCCCTTCT[C/T]TGGCTTGGTCAATTT | 55130 |
| rs150761167 | in-del | -/AC | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27939139 | AAAGATAAAACAGGA[-/AC]ACACACACACACACA | 55130 |
| rs150762743 | in-del | -/A | 0.0528381 | 0.153711 | intron-variant | ARMC4 | GRCh38.p7 | 10:27821266 | TTGAGTTTTGCCGCT[-/A]ACTAACTGTATTGTT | 55130 |
| rs150775169 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27897295 | ACTCATATATCTCCA[A/T]CCAGAATTCTCTCCT | 55130 |
| rs150779574 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27958351 | AAGACAGTTATCCAG[C/T]AATTAGGCTATTATG | 55130 |
| rs150780082 | snp | C/T | 0.00429751 | 0.0461551 | synonymous-codon, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983945 | ACGAATTTGTCTCCA[C/T]GGTGGGGCTCGACAT | 55130 |
| rs150794687 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARMC4 | GRCh38.p7 | 10:27854702 | TAGAGGTTGCAGTGA[A/G]CCCAGATCGCGCCAC | 55130 |
| rs150795941 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27883295 | GACCAATAAGCTGAG[C/T]AGAAACCTCTGGAGT | 55130 |
| rs150796485 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27948101 | TAAGAGTTTATAGCT[G/T]TTTGAAGTATCTCTA | 55130 |
| rs150829961 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27830199 | CCTTGGTCTCCTCAC[C/T]TCCTGGTTTCCCGGA | 55130 |
| rs150830607 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27900643 | TGGAGCTGAAAAACA[C/T]GGCAAAAGAACTTCG | 55130 |
| rs150835800 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | ARMC4 | GRCh38.p7 | 10:27990616 | CACTGACCCTACTAC[C/T]GTGACTTAGAAATTT | 55130 |
| rs150866608 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27941478 | CAACAAAGCAAGATC[C/T]TGCCCCCCGAACCAA | 55130 |
| rs150899463 | in-del | -/A | 0.0652144 | 0.168387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27879026 | CTAGACTTACATAAC[-/A]AAAAAAATGCATTAC | 55130 |
| rs150921485 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27877712 | TCACATGTCTTAAAA[A/G]CCTAGTCGTTGCCAG | 55130 |
| rs150940106 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27867599 | AATCAAGAAAGTAGC[A/T]GTGCCATCCTAGTCC | 55130 |
| rs150972802 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27814639 | TACTTGTTTGTTCTC[A/G]TCATGATCTCTTGTC | 55130 |
| rs150974197 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27907361 | ACAAATTTCTTATCC[C/T]TCAAGAGACAAGAAC | 55130 |
| rs151046182 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | ARMC4 | GRCh38.p7 | 10:27957029 | TTAGAGAGACTCATA[G/T]ATTTAGTATGGAGCC | 55130 |
| rs151061667 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27852682 | AAAGCTAACCGTGGC[C/T]GGGCACAGTGGCTCA | 55130 |
| rs151062642 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARMC4 | GRCh38.p7 | 10:27917173 | AAGAACTGAAATCAC[A/G]TATAATATCATCCCT | 55130 |
| rs151071850 | in-del | -/GTGT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27994006 | GTGTGTGTGTGTGTG[-/GTGT]TGTATTTGTTAGCTT | 55130 |
| rs151082311 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999259 | TGAGCAGTTGCGGGG[C/T]CGGCGGCAAGTTAGC | 55130 |
| rs151097323 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | ARMC4 | GRCh38.p7 | 10:27899116 | TGAGGTACCCATCTC[A/T]TCTCATTGGGACTTG | 55130 |
| rs151115819 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27856323 | TAAAACACAAGCTGA[G/T]TTTTCAACATAAGTG | 55130 |
| rs151131962 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27844265 | CAGCAAAGGAGGTTG[G/T]AAAATTGCTAAAACT | 55130 |
| rs151136207 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ARMC4 | GRCh38.p7 | 10:27938331 | GGCCCTGCTCCAATA[A/G]GACTGCTGTCCAAGG | 55130 |
| rs151147345 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27831659 | TACAGATGGCCTCCC[G/T]TGGCGTACGTGCCCA | 55130 |
| rs151187273 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | ARMC4 | GRCh38.p7 | 10:27875905 | GAGATTATATCGCAC[A/G]CCTGGCTCGGAGGGT | 55130 |
| rs151187854 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27942388 | GAAGTCTGGTGATAT[C/T]TTTGTGACCAGAAAA | 55130 |
| rs151193419 | snp | C/T | 3.36349e-05 | 0.00410077 | missense | ARMC4 | GRCh38.p7 | 10:27862615 | GAACGAACCATTTCC[C/T]CAGCATCCTAGACAA | 55130 |
| rs151254850 | snp | C/G | 0.021333 | 0.101051 | intron-variant | ARMC4 | GRCh38.p7 | 10:27921824 | TGAAGCAAGGCAATA[C/G]AGCAGTATTTTATTT | 55130 |
| rs151259662 | in-del | -/TAAGTA | 0.031825 | 0.122064 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997383 | GTCTGTCTTTAATCT[-/TAAGTA]TAACATTTGTTTTGG | 55130 |
| rs151271408 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27890362 | GAATATAATGACATA[A/G]TTTAATAGATGAAGT | 55130 |
| rs151276176 | snp | A/T | 0.0256215 | 0.110247 | intron-variant | ARMC4 | GRCh38.p7 | 10:27975653 | TTAAAATTTTTCCCA[A/T]AAAGAATATTCCAGG | 55130 |
| rs151287407 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27829552 | ATGTGGTTGTTATTT[-/C]TTTTTTATAACTTAT | 55130 |
| rs151304911 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | ARMC4 | GRCh38.p7 | 10:27861245 | GATCCACTCACTTTG[C/G]CCTCCAAAAGTGCTG | 55130 |
| rs151309252 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27927971 | TCTAATCTAACTAAG[C/G]TTTAGACATGAATAC | 55130 |
| rs151320891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27822630 | TCTTGCACATCCAGA[C/T]TCTGAGCCTCGGTAA | 55130 |
| rs151328338 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27980314 | AAAAATAGGTAAGAA[A/C]ATAAGAAAAAATAGG | 55130 |
| rs180673019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27973337 | CATCTGTACCAAAAA[C/T]AAAATAGTTTATTTT | 55130 |
| rs180684070 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27985291 | TTAAGACTAATAAAT[C/T]CTTCAAAGTCCATTC | 55130 |
| rs180699636 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27962130 | CTGTCTCTATTGCAG[C/G]TGCAATTGCTCTGGG | 55130 |
| rs180722165 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27946703 | CTTATATATAATAGG[G/T]TTAGCACAGAAAATG | 55130 |
| rs180726546 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27910799 | AAAAAAACAGATACA[G/T]TCAATTCTCATCAGG | 55130 |
| rs180733346 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27929410 | TGATTTTTGTCAGTT[A/G]TATTATTAAATTATA | 55130 |
| rs180738680 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27897842 | TCAAGAGAAATGGAA[C/G]AGGAAGAAGCTCTTT | 55130 |
| rs180756676 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | ARMC4 | GRCh38.p7 | 10:27879498 | GCTTATACTCAGTAA[A/C]CCACAGATTAAGAAG | 55130 |
| rs180759817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27865018 | GTGATCATTAGAAAC[C/T]GTAAATCTGATGATC | 55130 |
| rs180766139 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27844150 | CAGTGAGCTATGATC[G/T]TGCCACTGTACTCCA | 55130 |
| rs180826656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27995637 | TGAATACTGTTATCC[C/T]GACTTTCTTACAGTG | 55130 |
| rs180857512 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27913223 | TGTACAGATTATTTT[A/G]TTACCCAGATAATAA | 55130 |
| rs180874099 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27859229 | TCCAATATGTTTTTT[A/G]TAGTTTACTTTTAAA | 55130 |
| rs180879402 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27882549 | AATCAACATTTTCTA[G/T]AACTCTCAAATTTAA | 55130 |
| rs180902533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27876269 | GGGTCCCTGACTCCC[A/G]AGTAGCCTAACTGGG | 55130 |
| rs180907605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27869121 | CTATAAAGAATTAGA[C/T]ATAAAATAAAAATGC | 55130 |
| rs180913700 | snp | A/G | 0.0966517 | 0.197444 | intron-variant | ARMC4 | GRCh38.p7 | 10:27847174 | ATGCAAAAATCCTCA[A/G]TAAAATACTGGCAAA | 55130 |
| rs180917790 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27900697 | GCTGAATCGATCAGG[C/T]GGAAGAAAGGTTATC | 55130 |
| rs180927160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27838787 | GTATTTTTGACCCTC[C/T]AAAACTCTCTTTTTT | 55130 |
| rs180966754 | snp | C/G | 0.00438332 | 0.0466095 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999341 | CCTTTTTACATTTTT[C/G]CATAGGCTTCCAGAC | 55130 |
| rs180995889 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27978624 | ATGGGAAAACCCCAT[C/T]TCTACTAAAAATACA | 55130 |
| rs180998698 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27812749 | ACCAAAAAAGCATAA[C/G]AAATTCCATTTAAGC | 55130 |
| rs181003423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27831317 | CATCATCACCGAAAA[C/T]GACATTCCCCTGCCC | 55130 |
| rs181004350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27942317 | CTTTCTTAAATGTAC[A/G]TATAGGTCACAGTCA | 55130 |
| rs181008977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27959640 | TGTTTCCAAATTCCC[A/G]ACAGGTTAATCTTCA | 55130 |
| rs181009026 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | ARMC4 | GRCh38.p7 | 10:27924007 | AAGAAAGAAAGAAAG[A/G]AAGAAAGAAAGAAAG | 55130 |
| rs181019477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27906568 | CATGCACACGTATAT[A/G]TTTATTGCAGCACTA | 55130 |
| rs181037676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27822538 | CCTTTGGACTGTGTC[C/T]GCCTATGGAATGGCT | 55130 |
| rs181052739 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27817598 | GCAGTTTTGACTTTC[C/T]GTTTCTGAGTGATTT | 55130 |
| rs181058739 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ARMC4 | GRCh38.p7 | 10:27835851 | GAATCACTTGAACCC[A/G]GGAGGCAGGGGTGGC | 55130 |
| rs181077505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27893084 | GAATCGCTTGAACCC[A/G]GGAGGCAGAGGTTGC | 55130 |
| rs181081187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27932505 | GTGATATAGTCTATC[A/G]AGTGATACAAAAATA | 55130 |
| rs181107590 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27828590 | TCCATCTGAGTAATA[C/T]CCCTACTTAATGCAG | 55130 |
| rs181108070 | snp | A/C/T | 0.000390451 | 0.0139673 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983822 | CACTGGCTTTAGTTA[A/C/T]GTTTTTAAAAATTTA | 55130 |
| rs181114166 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ARMC4 | GRCh38.p7 | 10:27946168 | TCTACATTATGTTTA[C/T]ATATAAATTTAAAAG | 55130 |
| rs181123742 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27903277 | AAAACTCTCAATAAA[C/T]TAATTATTGATGGAA | 55130 |
| rs181139135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27887488 | ACTGTACCTAATGGA[C/T]ACATACAAAACACCC | 55130 |
| rs181141083 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27928849 | TCAGTCACTTTACTT[A/C]CATAAATTCACTTAA | 55130 |
| rs181145937 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27909889 | ATGACAAGAACATGA[C/T]TGAAAAACATTTGCA | 55130 |
| rs181151639 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ARMC4 | GRCh38.p7 | 10:27853140 | TTGGGAGGCCGAGGC[C/T]GGCAGATCACGAGGT | 55130 |
| rs181223701 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27919977 | TCAGATAAAACACTC[A/T]ATGCTTTCATTCAGA | 55130 |
| rs181235841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27879061 | TGAGGGTAGCTTTAA[C/T]GAATTGAATCACAAG | 55130 |
| rs181246328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27897388 | ATCTTTTCCTCAGAC[A/G]ATGTTATTCCCATGT | 55130 |
| rs181253258 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27843239 | AAAGTCTTAAAATAA[A/C]AACAGCCTATCTGCA | 55130 |
| rs181266422 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27821417 | ACCATCTGAAAAATA[C/T]GTAGCATATATGTGT | 55130 |
| rs181278667 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27838461 | GTTTCATAATTTCCA[A/G]TGGAAAGAATATATT | 55130 |
| rs181286777 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27864408 | ATGGGCTTGGAGCTT[A/G]GAAAAAAAAAACAGG | 55130 |
| rs181360262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27972420 | AGATAGTAAATTTAA[A/G]TTTAACTATATTAGT | 55130 |
| rs181410578 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27923324 | TATATCAAGCAAATG[A/G]AAACAGTAAGAAAGC | 55130 |
| rs181429868 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ARMC4 | GRCh38.p7 | 10:27906146 | ATATCCAGAATCTAC[A/G]AGGGACTTAAACAAA | 55130 |
| rs181432550 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27892842 | AGGTAGCTTTAAATG[C/T]TTCCAACAAGAAAAG | 55130 |
| rs181436561 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ARMC4 | GRCh38.p7 | 10:27990410 | TGAACTCCTGGGTTC[A/G]AGTGATCCTTCCATC | 55130 |
| rs181443240 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ARMC4 | GRCh38.p7 | 10:27875743 | GAGCCAAAGCAGGGC[A/G]AGGCATTGCCTCACC | 55130 |
| rs181450273 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27969317 | CTAGGTATGTATCGC[C/T]GCCAATTATAGTTTT | 55130 |
| rs181451054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27857994 | ATGCATTCGAAGTCA[A/G]AAATGTTAGCAGTCA | 55130 |
| rs181463807 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27951945 | CCAGGTATAGTGGCA[C/T]GCTCCTGTAGTCCCA | 55130 |
| rs181479214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27954946 | TGCAGATTCTGAGTA[A/G]GCTGTTTTTAGCTGA | 55130 |
| rs181484327 | snp | A/G | 0.000313954 | 0.0125251 | missense | ARMC4 | GRCh38.p7 | 10:27995117 | GCAGCAGTCCACTGC[A/G]TCAATTTCCTCAGAG | 55130 |
| rs181503170 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27998402 | ATTCGGTAAGGGGAC[A/G]AGGAGGGAAGGGACG | 55130 |
| rs181504931 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27959146 | GTTCAAGATCAGCCT[A/G]GGAAAGAGAAAAGGA | 55130 |
| rs181508417 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ARMC4 | GRCh38.p7 | 10:27933921 | GGTTAGACGAAGCCC[C/T]CTGATAGGATTTTGC | 55130 |
| rs181511510 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ARMC4 | GRCh38.p7 | 10:27901226 | CTAAGCTTCATAAGC[A/G]AAGGAGAAATAAAAT | 55130 |
| rs181530120 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27870623 | GGTTTTTTGTCCTTG[C/G/T]GATAGTTTGCTGAGA | 55130 |
| rs181623994 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27978175 | AATAATACACATCCA[C/T]AAAAGCAATAAATTA | 55130 |
| rs181635342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27914508 | CTCAATTTGTTACTT[A/G]ACATTATTCTATGAA | 55130 |
| rs181661129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27941825 | CTTCTGTCCCTGAAG[A/G]TCAACTTCCACAGAT | 55130 |
| rs181663726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27816386 | GTTTGGAGGGGCTCA[C/T]GCCTTGGGAGTTTTG | 55130 |
| rs181665623 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27884623 | CAGAGTCTAGATTTC[A/G]GCTAGCAGAAGCTAT | 55130 |
| rs181694818 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27848266 | CCTCAGAAATAATAC[C/T]ACACATCTACAACCA | 55130 |
| rs181722569 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27947424 | GAGCTATGATCACAC[C/T]ACCACTCTCCAGCAT | 55130 |
| rs181728302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27886946 | CAAAGAAAAGCAGTA[A/G]TGAAGAAAATGAGGA | 55130 |
| rs181728858 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27929810 | TTTGCTTCTTTTGCC[C/T]GGATGTACTTATTTT | 55130 |
| rs181734711 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27972246 | TTTGAGATATATATC[A/G]TAAGCCAGAGGGCAG | 55130 |
| rs181735694 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27993893 | TAAAAGTTCATATCC[A/G]GAACAAAGAAGAACA | 55130 |
| rs181745685 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27851494 | TGTCAAGTAGAGACA[C/T]GAAAGATGTGAAAGG | 55130 |
| rs181748713 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27910975 | GTATTTCTCTTTAAA[G/T]ACACCTTATTAAATA | 55130 |
| rs181757711 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27898385 | TATGTGAACCCTTAG[A/G]TGTTTCTGAGAATAT | 55130 |
| rs181762448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27880013 | AGAGCAGAGTGTAGC[A/G]GAATTCTTATCTTCT | 55130 |
| rs181845468 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27951567 | GAAAAAGAAGTGAAG[G/T]TAGATGCATACCTTC | 55130 |
| rs181854796 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27966822 | GAAAGATGAAGTAGA[G/T]ATACTTTTCCCTATT | 55130 |
| rs181864361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27985628 | TATGTGTGTGTAGCA[A/G]TGCTGGGTATTTATA | 55130 |
| rs181876074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27913647 | ACAAGCAAAAGCTGA[A/G]TAACCCCATTGAAAA | 55130 |
| rs181876457 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ARMC4 | GRCh38.p7 | 10:27900982 | CACAAAGATACTCCT[C/T]GAGAAGAACAACCCC | 55130 |
| rs181887415 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | ARMC4 | GRCh38.p7 | 10:27883713 | AAGAGAATTAAATTG[C/T]GTTAAAAATTAAATA | 55130 |
| rs181889171 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27869602 | TGAATTGGCACGATC[C/T]TGGCTCACTGCAACT | 55130 |
| rs181899753 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27848068 | CAGAACTGGAAAAAA[C/G]TACTTTAAAGTTCAT | 55130 |
| rs181901422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27919440 | AATAATGCATATGTG[C/T]TCAAAATATGTAATA | 55130 |
| rs181913644 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999873 | GCTCAAAGCAGAACC[C/T]TTCTGCAAACACGTA | 55130 |
| rs181927206 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27903068 | AAATACTGGCAAACC[A/G]AATCCAGCAGCACAT | 55130 |
| rs181931728 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27813317 | ATTTCCATCAAACTA[A/G]AGGCCATTTATTCCT | 55130 |
| rs181938708 | snp | A/G | 0.030278 | 0.119257 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872533 | GAGATACGTCCCATC[A/G]ATACCTAATTTATTG | 55130 |
| rs181995597 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27829105 | AAGCCAGAGAATTAA[A/C]AAGGAAAAAAAAAGA | 55130 |
| rs181998641 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872337 | CTTTTCCTAATTAAA[C/T]ACCCTTTATTTCTTT | 55130 |
| rs182059219 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27956306 | CCCTTTCCCCACTCT[C/T]CCACCTGGACTCTGA | 55130 |
| rs182065006 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27920581 | CTCCATTTGACACTT[C/T]TGCATCTCAGTTAAA | 55130 |
| rs182069846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27881657 | AACACTGAAAAGAAT[A/G]AGCCGGCAAAAATAC | 55130 |
| rs182069913 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27937446 | GGGTTCAGGTGATTA[C/G]AGACAAACAATTTCT | 55130 |
| rs182072898 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27903549 | TGTATATTTAGAAAA[C/T]CCATCGTCTCAGCCG | 55130 |
| rs182077616 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27867863 | CTGAGGCATGAGAAT[C/T]GCTTGAACCTGGGAG | 55130 |
| rs182085731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27846011 | CAACATTAGACAGAC[C/T]AATGAGACAGAAAGT | 55130 |
| rs182087718 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27888081 | AGGACACTTAAGGTG[A/T]TTCTGTATCTTTGCT | 55130 |
| rs182144563 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27835157 | AGGCCCTTGGAGGAG[C/T]GTCAAATCCTGCCAC | 55130 |
| rs182149219 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27830028 | ATGTGAACATACATA[A/T]GTAGGATAAAATGGA | 55130 |
| rs182174196 | snp | A/C/G | 0.00159649 | 0.0282165 | intron-variant | ARMC4 | GRCh38.p7 | 10:27936244 | CAAATGGTCATAAAG[A/C/G]TTACAAATACTTTAA | 55130 |
| rs182205084 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27834064 | CCCTGCTCTGCTCTC[C/G]AGCTTGGACATCCCG | 55130 |
| rs182206670 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27848567 | GACAAATGGGATCTA[A/G]TTAAACTAAAGAGCT | 55130 |
| rs182210369 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27979768 | CTGGAGAACTTAATA[C/T]GGTTAAGATGGCAAT | 55130 |
| rs182218051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27943447 | TTTAATCCTGTCATG[A/G]TTTTATACAATATTA | 55130 |
| rs182221659 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27831508 | CAGCAAACCTAGCTA[A/G]ATTTTATTATTAACG | 55130 |
| rs182293026 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27924536 | AATAAAAGAACAGTA[A/C]ATCCAGTTAATAAAA | 55130 |
| rs182344534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27814214 | TGCACTTCCTGACTC[A/G]CAGATTGAATCCCAG | 55130 |
| rs182346777 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27901648 | GGAAAGCAAAAAAAG[C/T]AGGGGTTGCAATCCT | 55130 |
| rs182350663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27931067 | GGGTCTCTGATGGCA[A/G]AGTCTTCACTTCTTC | 55130 |
| rs182353110 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27884946 | TTAGTGAAGGTCTTC[C/T]GAGCTGGTCTGCAAA | 55130 |
| rs182354684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27832461 | TTCTCTCTTGTCCCT[C/T]GTATCGCAGCCAGGT | 55130 |
| rs182356108 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27870924 | AGATCCTTGAGGAAT[C/T]GCCACACTGTCTTCC | 55130 |
| rs182378996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27899537 | CAGATCCCACTCCCA[C/T]GGAGCCCAGCAAGCT | 55130 |
| rs182407542 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27982480 | CTTTTGTCCCTTTAT[C/T]CCTAATTAGAGATTT | 55130 |
| rs182410357 | snp | A/G | 4.96167e-05 | 0.00498055 | synonymous-codon, intron-variant | ARMC4 | GRCh38.p7 | 10:27944288 | CTTGGCAACATTCGC[A/G]ATAGTCTCGGCTGCC | 55130 |
| rs182418402 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27960738 | ATGTTTACATTGTGC[A/G]ATGATTAAATCAAGC | 55130 |
| rs182429487 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27926198 | TAATGATGGTAACTA[C/T]ATTCTAATAAAACTT | 55130 |
| rs182460905 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27816072 | CTCATCTCCCCTATG[A/C]TGCATCCAACTGATT | 55130 |
| rs182462259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27960387 | GTTTTGCTCTTACCT[C/T]CCAGGCTGGAGTGCA | 55130 |
| rs182482888 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27990074 | TCGTGGAAGGGAGCT[A/C]AAAATTCTGTTTATA | 55130 |
| rs182493073 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | ARMC4 | GRCh38.p7 | 10:27850328 | CAGGCGCCTGTAGTC[A/G]CAGCTACTCTGGAGG | 55130 |
| rs182495174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, missense | ARMC4 | GRCh38.p7 | 10:27836031 | CCTCGTCATCTTCCC[A/G]TTGAGTAGCCTGAAG | 55130 |
| rs182569245 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | ARMC4 | GRCh38.p7 | 10:27963811 | AGTGAGTTTTTTAGA[A/C]CCCCATGCATTTGGC | 55130 |
| rs182579436 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27824451 | ATGTACTTGCTTCCA[C/T]CTACTGCCCTTCTGC | 55130 |
| rs182584748 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ARMC4 | GRCh38.p7 | 10:27874937 | TTCTCCTGGATAATA[C/T]CCTGCAGAGTGTTTT | 55130 |
| rs182595090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27855483 | GGAATGTCTGGAATG[A/G]GAGAAAAACACTCAA | 55130 |
| rs182612041 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27948018 | TTTGAGCTTTATTTC[A/G]TTAATTTTACTATAA | 55130 |
| rs182617527 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27911639 | TGCTGTTTCCCAGCC[A/G]TCTCCGTATTTTACA | 55130 |
| rs182682022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27853987 | AGAAAATATTTGCAA[A/G]TTACACATATGGTAA | 55130 |
| rs182701039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27991192 | TAAGAACAAAAGCAA[C/T]TGCAAATGATAATAC | 55130 |
| rs182712037 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27952410 | TTTTTTTTTTTTACC[G/T]TAAGTTCTAGGATAC | 55130 |
| rs182724910 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27895621 | TGCATATAACTCAAA[A/G]TTCAGTTATTTGGCC | 55130 |
| rs182730821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27963499 | AGGTGTCCTTAAATA[C/T]CAAAGTCACAAAGTC | 55130 |
| rs182734510 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27921974 | GGGTTCGAGACCCAC[A/G/T]TGGGCAACATGGTGA | 55130 |
| rs182739555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27915049 | ATAATCACAATCTTC[C/T]CCCAAATTGATGGCA | 55130 |
| rs182739885 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27986823 | TATTTTTAAGAAGAA[G/T]AAAAATATTTGCCAC | 55130 |
| rs182743941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27862123 | GAATCATAACCATGA[C/T]GGTGGCGGTGAAGAT | 55130 |
| rs182744669 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27947851 | TCCCATCCTAACATT[C/G]TTAATCGCTCGTGCT | 55130 |
| rs182751462 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27904303 | AGAAAGGCAAGGATG[C/T]TGTGTATGCGCGGGG | 55130 |
| rs182755449 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27890305 | TTCTGATCTGATCAC[A/G]ACAGCATGCATTGTT | 55130 |
| rs182831698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27987840 | ACAGTTTTTGTTTTT[A/G]TTTTCTAAAATGTGT | 55130 |
| rs182858665 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27991950 | ATGAGGTCATGGGGA[C/G]TGTTTTGATAATAAA | 55130 |
| rs182867167 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27925964 | TGAGCCAAGATGGTG[C/T]CACTGCACTCCAACC | 55130 |
| rs182870735 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27943874 | TGTAAAGCTTTTGAC[A/G]TTTTAAAGTTTTCAG | 55130 |
| rs182872514 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27970846 | GCGTGGTGGCATGTG[C/T]CTGTAATCCCAGCTA | 55130 |
| rs182886953 | snp | A/C | 0.00501997 | 0.0498476 | intron-variant | ARMC4 | GRCh38.p7 | 10:27907789 | TATCCTATCGTGGAA[A/C]CCAAAATCATGATAT | 55130 |
| rs182891412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27894908 | TCACTGTTCCTTAAC[A/G]CTGGAAACTTAATTA | 55130 |
| rs182893183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27877597 | AGTTTCTATGGAAAG[A/G]GAGGCAGTATATCTG | 55130 |
| rs182899583 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27880984 | GAGTAAGTCCCATAG[C/T]GAAAAAATTGGGGAG | 55130 |
| rs182909804 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27861605 | TAATACACCTTGGTT[G/T]CCTTGGCTCCTGAGA | 55130 |
| rs182916590 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27839670 | AGAAAAACGCTGTGG[A/T]TTAAACATAAAGTTG | 55130 |
| rs182917790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27845195 | GGTTACACACAAAGG[A/G]AAGCCCATCAGACTA | 55130 |
| rs182967695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27823477 | AACTGTATGTGACCT[A/G]AGGTAACTCTCTCTA | 55130 |
| rs182991609 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27963960 | GGCATGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 55130 |
| rs182996436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27969931 | GCCAACATGGCAAAA[C/T]GCCATCTCTACTAAA | 55130 |
| rs182999177 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27974306 | CAATTTTTGCTTTTG[C/T]TGCAATTGCAAATGG | 55130 |
| rs183000159 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27934327 | AAAGCCCTAATACAA[C/G]AGCTTTAAGTCACCC | 55130 |
| rs183005523 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27909069 | CAATGAAGGATTTGC[A/T]TTTCAAATTTAAATT | 55130 |
| rs183020443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27878511 | AAAGCACATACAAGG[C/T]GAGCGTAACATGACT | 55130 |
| rs183032546 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARMC4 | GRCh38.p7 | 10:27841014 | AGGCCACGGGTGAAT[A/G]CTCAGTAATTGATTG | 55130 |
| rs183041030 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27865732 | GATTGTTTGCAAACT[A/C]ATAGCCTTAAAAGAA | 55130 |
| rs183044736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27975048 | TTGGCTTGGCTGTTG[C/T]TGGCGTACAGGAATT | 55130 |
| rs183049127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27844868 | CGATGGGGTGGTGGC[A/G]AAGGAGTTGGATTTG | 55130 |
| rs183078977 | snp | C/T | 0.000353394 | 0.013288 | intron-variant, utr-variant-3-prime | ARMC4 | GRCh38.p7 | 10:27939876 | AAGAACGCCAACAAC[C/T]GCTGGGAGAGTTCAC | 55130 |
| rs183100073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27911385 | CTGATTTGGGGGTTA[C/T]AAATAAAGTTTAGAG | 55130 |
| rs183155636 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27885563 | AAATATATAAATATA[A/T]ATATATATATATATA | 55130 |
| rs183181586 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | ARMC4 | GRCh38.p7 | 10:27899205 | CTTGGGAAGCACAAG[G/T]GATCAGTGAAATCCC | 55130 |
| rs183195641 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27867108 | ACAATGGACAATATA[C/T]ACCATAGTAGGTGAA | 55130 |
| rs183202090 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27818610 | ATACGCAAATGAGAT[G/T]TAGAAAAAAATCTAG | 55130 |
| rs183206411 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27836203 | TTGAATACATATGCA[G/T]GTATATGTGTGTGTA | 55130 |
| rs183237111 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27960558 | TTTCACCATGTTGGC[C/T]AGGCTGGTCTTGAAC | 55130 |
| rs183241566 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27901979 | CATCTACATAACTCT[C/T]CACCCCAGATCAACA | 55130 |
| rs183252966 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27822988 | TCTATAGTATTGGGA[A/G]TAGAAATGGGATATA | 55130 |
| rs183286196 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27970142 | AATAAATAAATAAAT[A/G]AATAAATCTCTAGGT | 55130 |
| rs183298064 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27996135 | AATGAACATTTAATG[C/T]TTTTTTGGCAGATAA | 55130 |
| rs183325365 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27839095 | ATTTGTGATCAGAAA[A/C]ACTGTAACGTAGTCC | 55130 |
| rs183330940 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27991619 | GAGACCAACAAAAAA[G/T]GGGTAGCTTATCTAC | 55130 |
| rs183337096 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27953065 | GAGTTTGGGTATATG[C/T]ATATAAATCCAACAC | 55130 |
| rs183353932 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27916252 | CTAGGGGAAGGTGGC[C/G]TAACATGGGGAACTA | 55130 |
| rs183367612 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27901774 | TAACTGACCTAAATA[C/T]ATATGCACCCAGTAC | 55130 |
| rs183410439 | snp | G/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:28000851 | CAATTTTTCCTTGTC[G/T]TGATGAAACACTACC | 55130 |
| rs183424928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27934994 | ATAAAATCTTTCCAT[C/T]TCCAGGGCCACTTAC | 55130 |
| rs183466037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27916603 | CAGCCTGTTCAACGT[A/G]AAGATGACCAAGATG | 55130 |
| rs183551392 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | ARMC4 | GRCh38.p7 | 10:27988396 | GGATTGGAGTGCAGT[G/T]GCGTGATCTCGGGTC | 55130 |
| rs183570055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27956701 | TGGATTTACTGCCTA[C/T]AGGGTTAAAACCATA | 55130 |
| rs183597539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27905178 | TAAATTTCATCTTTT[A/G]TTTTATTATGAAGAC | 55130 |
| rs183599417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27869336 | ATCTCTACAATAGGG[C/T]ACATTTTAAAATCTA | 55130 |
| rs183600468 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27921767 | AGTAATTTACAAAGG[C/T]AAAATAATTAGACAA | 55130 |
| rs183609164 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27889699 | ACTTCAAGTCTCCCA[C/G]CCCTGTGTACTCAAT | 55130 |
| rs183614490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27847313 | TATAAACAGAACCAA[A/G]GACAAAAACCACATG | 55130 |
| rs183629862 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27854863 | TGAGCCACATAAGAA[G/T]GTGAATTAATACGAA | 55130 |
| rs183665355 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27981684 | ATTATTTTCATCTCC[A/G]AAGGATCTATATGGT | 55130 |
| rs183677788 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27953277 | ATTCATCTTTCATAA[A/G]TGAAATTTTATACCC | 55130 |
| rs183703275 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27814689 | CCTTTAACCATCTTC[C/T]GTCTTTGCTTCCTCC | 55130 |
| rs183759120 | snp | C/G/T | 0.0182019 | 0.0936463 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997373 | TGAAAGTTCTGTCTG[C/G/T]CTTTAATCTTAAGTA | 55130 |
| rs183763757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940395 | TGTGTATATATATCA[C/T]AGGTACTGATTTAAT | 55130 |
| rs183769814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27957909 | GAAAGTCAGGTCAAC[A/G]TGAATATTTCTCTGC | 55130 |
| rs183770045 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | ARMC4 | GRCh38.p7 | 10:27922531 | AAAAGGAAGGGAGAA[A/T]AAGAAAAATAGAATG | 55130 |
| rs183772909 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27900889 | ACTTGGAAAACACTC[A/T]GCAGGATATTATCCA | 55130 |
| rs183773104 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27883327 | ATGCATGACAAAAAA[C/T]GCATATTTTACAGAA | 55130 |
| rs183781567 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27907255 | AAAGCAACACAGAAC[A/G]TAGTGCTCTCTCACT | 55130 |
| rs183792647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27815708 | CCCCAAACAAAAATT[A/G]TTAGAGTTCATCAGA | 55130 |
| rs183795587 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27849413 | GTCGTGGGGTGGGAG[A/G]AGGGGGAGGGATAGC | 55130 |
| rs183797244 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27877421 | TTCAACAGGGTCCCA[G/T]AAGCTTCCTAATGAC | 55130 |
| rs183801944 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27938704 | TCCCAGGTTCAAGTG[A/G]TTCTCCTGCCTCAGC | 55130 |
| rs183822042 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27833688 | ATATCTGCTATGTTC[C/T]GCTCTGTGGCAGGCA | 55130 |
| rs183825660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27903715 | TTGCTACAAAGAGAA[C/T]AAAATACCTAGGAAT | 55130 |
| rs183838029 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27874657 | GGGTTGAAAATTCTT[C/T]TCTTTAAGAATGTTG | 55130 |
| rs183868067 | snp | A/T | 1.70571e-05 | 0.00292032 | intron-variant | ARMC4 | GRCh38.p7 | 10:27961728 | TTCCTAAGAACAATA[A/T]CAACACACATACACA | 55130 |
| rs183878259 | snp | A/C | 8.30613e-05 | 0.00644389 | missense, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983862 | TTTAAAAATACTCCT[A/C]CTGCACTGCAAGTAA | 55130 |
| rs183881395 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27946207 | TATTACATATAATAT[A/G]TAAATATAAAAAATA | 55130 |
| rs183917308 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27918124 | AAAAATAATCCTACA[A/C]GAAATCTATCAGAAA | 55130 |
| rs183927110 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27885795 | ATATATTATATATAA[A/T]ATATATAAAATATAT | 55130 |
| rs183934422 | snp | G/T | 0.0256215 | 0.110247 | intron-variant | ARMC4 | GRCh38.p7 | 10:27871721 | TTGGTCTATATCTCT[G/T]TTTTGGTACCAGTAC | 55130 |
| rs183938729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27850175 | ATTTGCTGGGCGTGG[C/T]GGCTCACACCTGTAA | 55130 |
| rs183972583 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27871177 | AGTGTCTGTTCATAT[C/T]CTTTGTTCACTTTTT | 55130 |
| rs183980433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27893318 | AACAATATAAAAAAA[C/T]GGATAACATCTGGTT | 55130 |
| rs183995914 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27988894 | AGATGGGGAGACTAT[A/T]CTGGGTATTTGGAGG | 55130 |
| rs184018297 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27965420 | TAGGGTGAGGATATA[A/C]GAAAATTCATTTCCT | 55130 |
| rs184018620 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27941961 | CTGGCTTGAGACAGG[C/T]GGACACTCCTGGTCT | 55130 |
| rs184029326 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27949651 | GGGCTGCTGGGCCCA[C/G]AGTCTGGGCTGAGAA | 55130 |
| rs184040814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27819951 | CAGCCTGGCTTCATA[C/T]GGGTTATGCATTTGA | 55130 |
| rs184054538 | snp | C/T | 1.64898e-05 | 0.00287135 | utr-variant-3-prime, missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27812510 | TAATGTCCATTTAAA[C/T]TTCAAGTGTATCTTG | 55130 |
| rs184086432 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27836471 | TTTGGGGACATCTTC[C/G]TAAATTATACTAATA | 55130 |
| rs184127241 | snp | C/G | 0.0310518 | 0.120672 | intron-variant | ARMC4 | GRCh38.p7 | 10:27875150 | AGTTGATTGAATCGG[C/G]TACTAAAGCTTGTGC | 55130 |
| rs184142340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27837131 | CCACACAATTCCACC[A/G]TTAAAAGACACCAGC | 55130 |
| rs184171788 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27896946 | CTCAATTCATTTCTC[A/G]CTCCAGTGCCATCCA | 55130 |
| rs184179150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27878877 | AAAAAATTATTGCTG[C/T]TTTAGACTTACCTTA | 55130 |
| rs184182813 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27864276 | TAATGTTGGAAGAGC[C/T]GGGTTTGGTTTGACT | 55130 |
| rs184191006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27842522 | TGGAGTGGATAACTA[C/T]TTTTCACAAATAGTT | 55130 |
| rs184267650 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27891189 | TGTTCTGTCACACCT[C/G]TGGTCAGGAAACTGG | 55130 |
| rs184277182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27856946 | CACTCCAGCCTGGAC[A/G]ACAAGACCGAAACTC | 55130 |
| rs184303483 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | ARMC4 | GRCh38.p7 | 10:27945656 | AAACAAAACCCAAAA[G/T]ATTAAAAATAAAAAA | 55130 |
| rs184308449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27966526 | TTTAAAATGCTTTTC[C/T]TATTTGATATGATTT | 55130 |
| rs184309480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27961480 | CTTATTTGAAAGAAA[C/T]GTAAAGTAAACTTGG | 55130 |
| rs184312997 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27932628 | AGGTTCTCCATGTTG[A/G]CTACTCCTGTCTGAT | 55130 |
| rs184313548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27927662 | TACCAGGCCTTGCTA[C/T]AGAATTTAACATGTT | 55130 |
| rs184324544 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | ARMC4 | GRCh38.p7 | 10:27909755 | CCCAGGAGGTGGAGG[A/T]TGCAGTGAGTCGAGA | 55130 |
| rs184365194 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27821069 | ATAGGCGTGAGCCAC[C/T]GTGCCCAGCCAGCAT | 55130 |
| rs184415791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27989774 | GATCACTTGAGCCCG[A/G]GAGGCGGGAGGATGC | 55130 |
| rs184424273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27820429 | GGACTGTGAGTGTCA[A/G]GCATATGAGTCATAA | 55130 |
| rs184426543 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27951359 | AAATATCAAAATATA[A/C]CAATGCTGTAGTAAT | 55130 |
| rs184442290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27948992 | TAATTTCCTCAACTA[C/T]GTTTTTTTAATTACT | 55130 |
| rs184448656 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27953670 | TATTAAATATAAAAA[G/T]CAAAATGTAGAATAA | 55130 |
| rs184455566 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27931970 | ACCTACTGAACATCA[C/T]AGCTTAGACTAGCCC | 55130 |
| rs184458686 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27913267 | TAGGTAGTTTTTCGA[C/T]CCTCACCCTCCTCCC | 55130 |
| rs184461894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27929130 | GACTGTACAGAAAAA[C/T]ACAAAGCATTAACAA | 55130 |
| rs184463643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27912281 | AAATTAATTTCTTGA[C/T]ATTATAAAAACAAAA | 55130 |
| rs184464457 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27899816 | GAAGCAGCTCCAGTC[A/C]GGAGCTTATACATAA | 55130 |
| rs184467239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27857102 | GCACGAGTCCACTTA[C/T]ATGTGGATTTTCTTC | 55130 |
| rs184473428 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27897413 | CCATGTTTGGTAAAA[A/C]TTCTATCATGTTCCT | 55130 |
| rs184474116 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27815371 | ACCCCATTTTCTTCC[A/C]TTCATAGCCAAATTT | 55130 |
| rs184474654 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARMC4 | GRCh38.p7 | 10:27837793 | GAACACAGCATCCGC[A/G]AGCCCTGACTTGTCA | 55130 |
| rs184474784 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27881983 | CCAGACTCGACAACA[C/T]GGTGAAACCCTTTCT | 55130 |
| rs184481423 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27868043 | AACAAACACTTCTCA[A/G]AAGAAGACATTTATG | 55130 |
| rs184481844 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | ARMC4 | GRCh38.p7 | 10:27994246 | TTAAGAATTCTCTCC[C/G]TTATATTGGGCAAAA | 55130 |
| rs184586455 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27910092 | TTTCATATCAGGATC[A/G]TTGTGTGAGGGAATA | 55130 |
| rs184590820 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27971470 | AACATCAAGACTAAG[C/G]CTTCTGTTGGAGTTA | 55130 |
| rs184597266 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27824859 | GGGGAAAGGTTGTAT[A/G]TATAAAATAGTCAAA | 55130 |
| rs184602729 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27935300 | TTTTGTATAAGGTTT[A/G/T]CTAAAAATTACTAAA | 55130 |
| rs184617399 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ARMC4 | GRCh38.p7 | 10:27841748 | CTCCAAGAGTGATCA[C/T]CTTTTTTTGTTTGTT | 55130 |
| rs184629862 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27992106 | GATGTTAAAGCATCT[G/T]GTACTTTCCATTATG | 55130 |
| rs184704340 | snp | A/C | 0.00159649 | 0.0282165 | intron-variant | ARMC4 | GRCh38.p7 | 10:27897941 | TAGGCTGCTTGCATA[A/C]GAGACCAGCCAGATA | 55130 |
| rs184773881 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27978389 | CATTACTCTAGAAAC[A/T]TCTGAGATAAAATAA | 55130 |
| rs184783242 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27878681 | CATTAGAATAGCATG[A/T]CAGAGAAGTGAAAAC | 55130 |
| rs184788713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27831001 | AGATACTGCTGATCA[A/G]CTGAGATGTGATGTT | 55130 |
| rs184789090 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27863309 | AATAACCAACAAAAA[C/G]CACAAAAATCCAAAA | 55130 |
| rs184802570 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997878 | TAAATACACAGCACA[C/T]ACCTTTGAAGTAAAG | 55130 |
| rs184829476 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ARMC4 | GRCh38.p7 | 10:27912816 | AATTCAGTAAAATGG[A/G]AAACATAAATGTATG | 55130 |
| rs184857967 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27882228 | GAAAGAAAGAAAGAA[A/G]GAAAGAAATATGAAC | 55130 |
| rs184870091 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27847039 | AACTATTCCAATCAA[C/T]AGAAAAAGAGGGAAT | 55130 |
| rs184897637 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | ARMC4 | GRCh38.p7 | 10:27998515 | CGGCGGGAGAAGTGG[A/G]GAGCGGATCCGGGAG | 55130 |
| rs184906532 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27959295 | GAAGGAAGAAAGGAA[A/G]GCAGGCTAAGCCCCA | 55130 |
| rs184914969 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27992655 | GATCACTCCACTGCA[C/G]TCCAGCCTGGGCAAC | 55130 |
| rs184929732 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ARMC4 | GRCh38.p7 | 10:27971837 | ATAAAACAAAAATCT[C/T]TCAAAAATGAAAGCA | 55130 |
| rs184943268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27932317 | AGTTATTGAATACTG[C/T]ACTGAAATTGAAGAA | 55130 |
| rs184945539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27954105 | TTTATACCAAATCTG[A/G]TGCCTCTTATTCACT | 55130 |
| rs184947146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27900673 | GTGAAGCATACACAA[A/G]TACCAATAGCTGAAT | 55130 |
| rs184953608 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27919041 | TATTGCTGAGAGAAA[G/T]GAAAGACCCAAATAA | 55130 |
| rs184959049 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ARMC4 | GRCh38.p7 | 10:27935955 | TACAGAACATTTTCC[C/T]TTCCTAATAAATTTC | 55130 |
| rs184971694 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27868749 | AATACCTAGGTGATG[A/G]GTTAATAGGTGCAGC | 55130 |
| rs184972566 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | ARMC4 | GRCh38.p7 | 10:27902779 | TGAATAGACCAATAA[A/C]AAGTTCTGAAATTGA | 55130 |
| rs185004865 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27871382 | CCATTTGTCAATTTT[C/T]GCTTTTGTTGCCATT | 55130 |
| rs185016198 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27978839 | AGGCAACTTCCTCAA[A/C]ATGCTAAAGGTCATA | 55130 |
| rs185024580 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27943275 | TTACAAAAGCAAGAC[A/T]TAGACAAAGAAGACA | 55130 |
| rs185028412 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27916040 | ATATTAGAACCTAAA[C/T]AGAGTGATTGAAGCA | 55130 |
| rs185030468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27959875 | AAAAAACTTATGTAA[C/T]AAATGCATGATTTAT | 55130 |
| rs185042875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27924361 | AAGTACTATACATCA[A/G]AATTACAGGGTACAT | 55130 |
| rs185103228 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27885697 | ATATATAATATATAA[A/T]ATATATAAAATATAT | 55130 |
| rs185118017 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27833204 | TGCATGCTTTCTAAA[G/T]TTACAGTCTGATTTA | 55130 |
| rs185123625 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27849757 | AAGCAAAGTGCTAAA[G/T]AAATGTGAAAAAATA | 55130 |
| rs185137228 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27817671 | AAGACATGATTCATT[A/C]TTTTTTATGACTGAG | 55130 |
| rs185143809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27835868 | GAGGCAGGGGTGGCA[A/G]TGAGCCGAGATTGCA | 55130 |
| rs185175884 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | ARMC4 | GRCh38.p7 | 10:27887937 | AAGTTGGATAACCTA[G/T]ATGAAATAGACAAAT | 55130 |
| rs185187909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27830213 | CCTCCTGGTTTCCCG[A/G]AATGTCTTTCTCACC | 55130 |
| rs185193452 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27853532 | ACCAAGGGTGTCTAT[A/G]TTAGTATCAGAAAAT | 55130 |
| rs185239322 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983640 | TTTCTTATCAGATTG[C/G]CTTAATGACCTGCAG | 55130 |
| rs185249904 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ARMC4 | GRCh38.p7 | 10:27827364 | ATAGCAGACACACAC[A/G]TACACACACACACAC | 55130 |
| rs185279155 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27812928 | CTTTTCTGTCTTTTC[C/T]ACCTCTCAGAACAAG | 55130 |
| rs185289782 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27922953 | CAAACAAAAAACAAA[A/G]AAAACTAAATAGTGA | 55130 |
| rs185303321 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | ARMC4 | GRCh38.p7 | 10:27892458 | CTTTGTAAAACAGAC[G/T]CTCATTTCACACTCC | 55130 |
| rs185354304 | snp | A/G | 0 | 0 | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27936657 | CTCCTTACTAGAATG[A/G]CATTAAATGACAAGA | 55130 |
| rs185362176 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27919979 | AGATAAAACACTCTA[C/T]GCTTTCATTCAGATA | 55130 |
| rs185364471 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27903295 | ATTATTGATGGAATG[C/T]ATCTCAAAATAATAA | 55130 |
| rs185386504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27941192 | TATACACCTTAAAGC[C/T]ACAAGACCTGTCCAG | 55130 |
| rs185406129 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27905830 | TGCAGAAAACTGAAA[C/G]TGGACCTCTTCCTTA | 55130 |
| rs185432170 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27875659 | CATTTCCAACTGAGG[C/T]ACCAGGTTCATCTCA | 55130 |
| rs185460162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27846902 | CCCTCAATAGATCAA[C/T]TGTTGCTCTGAAATT | 55130 |
| rs185495957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27923817 | AGCTGGATGTGGAGG[C/T]ACATACCTGTAGTCC | 55130 |
| rs185521537 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ARMC4 | GRCh38.p7 | 10:27906404 | AGGAATGCTTTTACA[C/T]TGTTGGTGGGAGTGT | 55130 |
| rs185526016 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27892870 | AAGATGTACTACGGC[A/C]GGGTGTGGTAACTCA | 55130 |
| rs185540168 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, synonymous-codon | ARMC4 | GRCh38.p7 | 10:27858179 | GCAAATATCAAATTA[C/T]GATTCTACCAACACC | 55130 |
| rs185550842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27838563 | TGGTTTAGCAAAAGG[A/G]CCAAGTCGGAAGGAA | 55130 |
| rs185555601 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27986913 | GAGAAAAGTGGAAAG[A/G]GAGACTATTAAAGGC | 55130 |
| rs185581175 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983170 | ATTTTTCACGGTCCC[A/T]GAAACAGGCTCACCT | 55130 |
| rs185598192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27813908 | AGGAACAAATTCAAG[C/T]GATATTTGGGATGAA | 55130 |
| rs185607419 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27831963 | TGCCTGCCTTGACCC[A/C]CAGTGCATCATTGCT | 55130 |
| rs185614747 | snp | C/T | 1.64833e-05 | 0.00287078 | missense | ARMC4 | GRCh38.p7 | 10:27944833 | TACATTTGACTTCAT[C/T]GGTTTCAAGCAAATT | 55130 |
| rs185620371 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27886785 | GTTGTATACAATTGA[A/G]ATGAAGTTACTATCA | 55130 |
| rs185624669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27909275 | GACAGAAATAACTTG[C/T]CATTGCAGTGGAAGT | 55130 |
| rs185635557 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ARMC4 | GRCh38.p7 | 10:27850436 | GGCGACAGAGCGAGA[C/T]TCCGTCTCAAAAAAA | 55130 |
| rs185653830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27816172 | ATTCACCCCAGTAAA[A/G]CCTACTTCCCACTGT | 55130 |
| rs185671137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27852731 | TTTGGGAGGCGGAGG[C/T]GGGTGGATCACCTGA | 55130 |
| rs185729453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27961001 | GGCCAATTATTATGT[A/G]AAATATTCTCATATA | 55130 |
| rs185756375 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | ARMC4 | GRCh38.p7 | 10:27926689 | AAATTTAGCAGAAAA[A/T]TTTTTACAAAGAAAG | 55130 |
| rs185759676 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872338 | TTTTCCTAATTAAAT[A/G]CCCTTTATTTCTTTC | 55130 |
| rs185761985 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27896467 | AATAGATGGATGATT[G/T]ATTGAAAGATAGAGA | 55130 |
| rs185794642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27834120 | GACACAAAAGTAGCA[A/G]ATGATTGCCAAGACA | 55130 |
| rs185849267 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27817209 | TTATCCTAACACATG[A/G]CTTACATGTCTTTGT | 55130 |
| rs185855677 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27835599 | TACTGTTGCTCAGAA[G/T]CCTTAACAATAACAT | 55130 |
| rs185873552 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27990748 | CAAAGCTAAGGTCCA[A/G]AAAGGTATAAATTGT | 55130 |
| rs185878178 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27969978 | AGCCGTGGTGTCACA[A/C]ACCTGTAATCCCAGC | 55130 |
| rs185880126 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27934490 | GGATATATCTCTCTA[C/T]ATGTATATTGTATCT | 55130 |
| rs185888359 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ARMC4 | GRCh38.p7 | 10:27969339 | TATAGTTTTCTATTT[C/T]CTTATCTTCCCCACC | 55130 |
| rs185922823 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ARMC4 | GRCh38.p7 | 10:27906644 | ATAGACTGGATAAAG[A/G]AAAGGTGGCATTTAT | 55130 |
| rs185938672 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27876706 | GAGTCATCACAGGTC[A/G]CACCAAGGAATGGCA | 55130 |
| rs185955876 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27838958 | AAAAGATGCTTCAAC[A/G]TGTGCCAGCATCATC | 55130 |
| rs185991352 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ARMC4 | GRCh38.p7 | 10:27991235 | GATTTCCATGAAATG[A/G]AAGTAGAGCTATTTG | 55130 |
| rs185997468 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27952412 | TTTTTTTTTTACCTT[A/C]AGTTCTAGGATACAT | 55130 |
| rs186000332 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27829002 | AAATTCGAAACCAAA[G/T]ACAAGCCAATATTTA | 55130 |
| rs186016746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27986252 | TTACAAAAAGAGCAG[A/G]CAGATTCTGAGGAAT | 55130 |
| rs186026620 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27947596 | GCTCTTTTTTTCTCT[G/T]AATTTAAATGGTTAA | 55130 |
| rs186030758 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ARMC4 | GRCh38.p7 | 10:27963100 | GCAACCTCCGCCTGC[C/T]GGGTTCATGTGATTC | 55130 |
| rs186044800 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27929833 | CTTATTTTTTCCCTT[C/G]TGAAATGCAAGTAAT | 55130 |
| rs186053355 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | ARMC4 | GRCh38.p7 | 10:27910997 | TATTAAATATAGATT[G/T]TTGAATCATGAATAT | 55130 |
| rs186053632 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27893214 | AAAAGAGAAAAGAAA[G/T]AAAGAAAAGATGTTC | 55130 |
| rs186067510 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27880263 | AATCTTTTAGATATA[A/T]ATTTCACCTTGTGAA | 55130 |
| rs186072797 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27859277 | AAAGATGCTTTGGCC[A/T]GATTTTTGCTTGAAG | 55130 |
| rs186074920 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27822549 | TGTCCGCCTATGGAA[A/T]GGCTTCCCAACTATT | 55130 |
| rs186091620 | snp | C/T | 0.0501905 | 0.150254 | intron-variant | ARMC4 | GRCh38.p7 | 10:27864579 | GGAGTGAGGTGAGAA[C/T]GGGGAGTGAGGTGAG | 55130 |
| rs186163710 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27823121 | TATATCAGAGGAAAA[G/T]GAAGTGATAAGTTTC | 55130 |
| rs186195170 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27877495 | AGGTCCCTCTGAAGT[C/T]TATTTGTTTTGAAGG | 55130 |
| rs186201656 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27901019 | CATAATCATCAGATT[C/G]AGCAAGATTGAAATG | 55130 |
| rs186210385 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27839110 | AACTGTAACGTAGTC[C/T]AACATTCCTAATTTT | 55130 |
| rs186211497 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27879429 | GTCTTTTATATAGGA[A/C]TATATGTATATATTA | 55130 |
| rs186218115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27995215 | GAAAGAGACAACAGC[A/G]TCCACCTTTTCCTTG | 55130 |
| rs186220229 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27955616 | ATTAACTGTAATTGA[C/T]TGCAAAGTACATCAA | 55130 |
| rs186231996 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27843405 | CCAGCATAACTGGGT[A/T]AAAAAGCAACTGGCT | 55130 |
| rs186258695 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | ARMC4 | GRCh38.p7 | 10:27921313 | CGAAAAAAAAAAAGA[A/C]AAAAAAAAGAACATG | 55130 |
| rs186325655 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27967173 | GACCACACATAACAG[C/T]GTGGCCCAAGTCTAC | 55130 |
| rs186330909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27990171 | TTTTTTTTAAGAGAC[A/G]AGATCTTGCTCTGTC | 55130 |
| rs186338260 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27951651 | AAAGCTATAAAACTA[A/T]CAGAGGGAACTAGAA | 55130 |
| rs186352469 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27913748 | TGTTCAACATCACTG[A/T]TCATTAGAGAACTGC | 55130 |
| rs186353406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27972512 | GAAAAGGAGACCTAA[C/T]TATTTGTGGCCTAAA | 55130 |
| rs186357513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27933683 | AGATCAAAAGAAATA[C/T]ATGCAGCCATTTCTG | 55130 |
| rs186360630 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27951979 | GCTTGGGAGGCTGAG[A/G]CAGGAGAATTGCTTG | 55130 |
| rs186360985 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27914618 | TAATGACCAATTTGT[G/T]GTTATCTCCTCTGTA | 55130 |
| rs186384712 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27884809 | TTTAAGAACAGCCAT[C/G]TATATGGGGGAAAAA | 55130 |
| rs186399481 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27848379 | GCCATATGTAGGAAG[C/G]TGAAACTGGATCCCT | 55130 |
| rs186424962 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27995667 | GACAATATCTGCATC[A/C]TCACAATGATGACTG | 55130 |
| rs186439480 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27974061 | TTTTTCACATGCTTG[C/T]TGGCCACATGTATGT | 55130 |
| rs186449008 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27938184 | CCTCAGGTTATCCAC[A/T]CACCTCGGCCTCCCA | 55130 |
| rs186454420 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27956364 | TCCCACAGGGAGGAG[G/T]TACATGTGGAGAAAT | 55130 |
| rs186466778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27897959 | GACCAGCCAGATATT[C/T]AGGAAAGAAAGCCCA | 55130 |
| rs186468487 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27814358 | GGGGACCCCTTCCCA[C/T]CCGGCTGTCTCAATG | 55130 |
| rs186473756 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27879631 | ATCTAACTATATGAT[A/G]TATTATACTCCAAAA | 55130 |
| rs186478730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27821781 | CTATTTTTTTATCTA[C/T]AGACTTTCTTTCCAA | 55130 |
| rs186480110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27865075 | CACAGCAACCCCTGC[C/T]CTTAGGATAAAATTC | 55130 |
| rs186489249 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27844214 | CAAAAAAAAGAATAA[C/T]TGGCATAAATTAAGA | 55130 |
| rs186533277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27829292 | CTAAATCGGAACTAA[A/G]CTCATAAAGATGAAA | 55130 |
| rs186555752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27933926 | GACGAAGCCCCCTGA[C/T]AGGATTTTGCTGTGT | 55130 |
| rs186582886 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | ARMC4 | GRCh38.p7 | 10:27901328 | GCACTAAATTTGGAA[A/C]GGAAAAACCGGGACC | 55130 |
| rs186602432 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | ARMC4 | GRCh38.p7 | 10:27870689 | GGACATGAACTCATC[A/C]TTTTTTATGGCTGCA | 55130 |
| rs186611278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27901712 | GATCAAAAAAGACAA[A/G]AAAGGGCATTGCATA | 55130 |
| rs186621323 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27885211 | AAATGAGAATATAAA[C/T]AAGGAGACAGAAAAA | 55130 |
| rs186626163 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27871040 | TGACTTTTTAATGAT[C/T]GACATTCTAACTGGT | 55130 |
| rs186632333 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27848633 | AGGCAACCTACAGAA[C/T]GGGAGAAAATTTTTG | 55130 |
| rs186687205 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944493 | ATGTTTTTAAAAATT[C/G]CGAGTATACCTAAAA | 55130 |
| rs186695517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27972348 | CTCAATTCAAAAGGG[A/G]CAGAGGAAGGAAAAA | 55130 |
| rs186699360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27936295 | TGTTTGAAAATGACC[A/G]CTCTTTAAAGAGTAA | 55130 |
| rs186726923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27829848 | AGACTGTGTTCATTT[C/T]AGAGCCCATCTTACA | 55130 |
| rs186736571 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27903163 | TGCAAATCAATAAAC[A/G]TAATCCATCACATAA | 55130 |
| rs186745370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27844906 | AGAAGCAAGGTGGAT[C/T]CATTATAGTGAAGCA | 55130 |
| rs186752814 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872655 | TTATATGCTGGATTA[C/T]GTTTATTGATTTGCA | 55130 |
| rs186808627 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27831732 | TTGGCATTTTCTGAG[A/G]CATAGCTGGTCCTCT | 55130 |
| rs186879425 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27960823 | AAGAAACCATGAGTT[A/G]AGTCAAATACTTTTT | 55130 |
| rs186887741 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27982617 | TCAGAAAGATAACTA[C/T]AGGTAATCAGAAAAG | 55130 |
| rs186904661 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27869758 | CAGGCTGGTCCCGAA[C/T]TCTTGACCTTAAGTG | 55130 |
| rs186940808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27919566 | AAGTTACTCAATACC[A/G]TTAGTTATCAGAAAA | 55130 |
| rs186947429 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27866770 | TGGGAACTAATAGAC[C/G]AAGAAGAACTCACTC | 55130 |
| rs186950408 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27887074 | AAATACATTGGCAAA[A/G]TGGATTTTAAAAAAA | 55130 |
| rs187004906 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999896 | AACACGTAGGGATAT[A/G]AGGTATAGATATTTG | 55130 |
| rs187008900 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27957367 | CCCCTTCACACCATC[A/G]GGGCAGAGGTAGGGA | 55130 |
| rs187017714 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27813493 | AAACAAATGAATTAG[A/G]ACATTTAAAATCTAG | 55130 |
| rs187020983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27922038 | CGGGCATGGTGGGAT[A/G]TGCCTGTAGTCCCAG | 55130 |
| rs187023198 | snp | C/T | 0.000312045 | 0.012487 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940033 | AAACCTACATATTTA[C/T]GTGTTCAAGACGTGA | 55130 |
| rs187041250 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ARMC4 | GRCh38.p7 | 10:27904454 | GCACTCCAACCTGGG[C/T]GACAGAGCGAGACTC | 55130 |
| rs187041778 | snp | C/T | 0.0298908 | 0.118541 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27960435 | CACTGCAACCTCCGC[C/T]TCCTGGGTTCAAGCA | 55130 |
| rs187044988 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27890969 | AGTTGATTATTTGGC[A/C]CCATGTCATACAGCG | 55130 |
| rs187052245 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27875137 | TACCCTTTCTTCCAG[C/T]TGATTGAATCGGCTA | 55130 |
| rs187060682 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27856337 | ATTTTTCAACATAAG[A/T]GGATCAGGAAATCCT | 55130 |
| rs187066998 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27925920 | CTGAGACAGGAGAAT[A/T]GCTTGAGCCCGGGAT | 55130 |
| rs187080729 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | ARMC4 | GRCh38.p7 | 10:27893550 | TGCCATTAATCCAAA[A/C]AAAGACGTTATTTCA | 55130 |
| rs187109622 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27848165 | CACACTACCTGACTT[C/T]AAACTATACTACAAG | 55130 |
| rs187177081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27907846 | ACATTTTAATGACCC[A/G]CTTATTTAATTATTT | 55130 |
| rs187187480 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27849988 | TCTGTCAGGGGAACC[C/T]GAAGTTCCATGAGTC | 55130 |
| rs187188928 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27895143 | GTTTCTAAAACTTAT[A/C]TAATGAACATGTAAG | 55130 |
| rs187190662 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27877867 | ACATGCATTATCTCA[C/T]ATGATCTTCACAACG | 55130 |
| rs187197740 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27946920 | AAATTTCTTCCATGC[C/T]TCTAGAAATGTCCTC | 55130 |
| rs187198369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27861979 | AAGGCTGCTTATTCT[A/G]TCTGGCACAGCTCTG | 55130 |
| rs187209325 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27888130 | GATAAACATACAAGT[A/T]CATGTATCTTTTTGA | 55130 |
| rs187220949 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27980408 | AAGGCAACCTGCAGA[A/G]CAAGAGAAAAAATTT | 55130 |
| rs187252053 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | ARMC4 | GRCh38.p7 | 10:27943568 | AAGGTGGGCGGATTA[C/T]CTGAGCTCAGGAGTT | 55130 |
| rs187259695 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27907279 | TCTCACTGCAGGCTG[C/T]AAGGACAATAGAAGC | 55130 |
| rs187294433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27932023 | TACTGCAGCCTCAAA[C/T]TCATGGGCTCAAGCA | 55130 |
| rs187299226 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27912305 | AACAAAACTGAATTA[A/C]ATGCTTTCAAGATCT | 55130 |
| rs187303408 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27900031 | CTGGGAGACACCTCC[C/T]AGCAGGGGTGGACAG | 55130 |
| rs187324636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27815513 | AGTAACTTCCTTCCA[C/T]GTGGCTAAGAGTAGT | 55130 |
| rs187324661 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27981768 | ATCTATTTTTCCATT[A/C]ATTCACTCATTCCTT | 55130 |
| rs187330480 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27833322 | GCACCCGGCAATAGT[C/T]GTACTTCGCAATGAT | 55130 |
| rs187332306 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944016 | TCCTATTTCTTCAAA[A/C]AATGAGTTTGAAGAT | 55130 |
| rs187335186 | snp | C/T | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27960590 | CCTGACCTCAGACGA[C/T]CCACCCTCCTCGGCC | 55130 |
| rs187340182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27925990 | CAACCTGGGTGACAG[A/G]GTGAGACTCCAGCTA | 55130 |
| rs187371530 | snp | A/G | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27819378 | TGAGAGAGATATACT[A/G]TGAAAGATTAAGGAC | 55130 |
| rs187392191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27962355 | AAGTGCTCAATGGCC[C/T]ACGTGCCTCGTGGTT | 55130 |
| rs187408448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27903621 | GGATACAAAATCAAT[A/G]TGCAAAAGTCATAAG | 55130 |
| rs187409828 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27929458 | AATATAGATGACTCT[C/T]CCTAATGATGATTCT | 55130 |
| rs187412951 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27985428 | TCTAGTTTGTATTGT[A/T]ACATCATCTATATAT | 55130 |
| rs187423434 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ARMC4 | GRCh38.p7 | 10:27874312 | GACTCTTTACCCACT[C/T]TGCCAGTCTGTGTCT | 55130 |
| rs187443156 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27964486 | ATATTCATTCACCAA[A/T]CGTGCATGGAGGGCC | 55130 |
| rs187447905 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27988604 | CGACCTCCCAAAGTA[A/C]TGGGATTACAGGCGT | 55130 |
| rs187452591 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27949433 | TGGAGCATCACTCAC[A/C]GGGAAAGAACATCTG | 55130 |
| rs187482427 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27874706 | CTTTTGTCTTGTAGG[A/G]TTTCTGCCGAGAGAT | 55130 |
| rs187491197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27855317 | TGAACTTCTTTCTCA[C/T]TTTACAGGAGAAATA | 55130 |
| rs187495864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27836324 | TGGGTGACTTGGCAG[C/T]AGAACTCAGGGCCAG | 55130 |
| rs187534229 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | ARMC4 | GRCh38.p7 | 10:27909232 | CGCAGCAAATTTGGC[A/G]TTAGTGATATTTAAC | 55130 |
| rs187549361 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARMC4 | GRCh38.p7 | 10:27878566 | GAGCTATAAAAACAC[C/T]ACTCTGGGCCATATA | 55130 |
| rs187561091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27970380 | TCGCTGATTAGCTCC[A/G]TATAATTTTCATCAT | 55130 |
| rs187564605 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27841459 | GGAGTGCAGTGGTGC[A/G]ATCTCAGCTCACTGC | 55130 |
| rs187567067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27991637 | GTAGCTTATCTACTT[C/T]GGCAGAATTTCAGCG | 55130 |
| rs187573340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27953120 | AGTAATAAATATATC[C/T]ATCACCTGAAAACAT | 55130 |
| rs187586119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27896721 | TTTTTCTCCATCTGT[A/G]CTTGTGTATGTGTAC | 55130 |
| rs187598963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27916481 | ATACAGTTGACCCTT[A/G]AATAACATGGGTTTG | 55130 |
| rs187600461 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27934690 | CCTGACACTCTCTAG[A/G]AGCCTAGTTAGATAG | 55130 |
| rs187622562 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27901951 | CAGCTCTGGAACAAG[C/T]GAACCTAATAGACAT | 55130 |
| rs187710143 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27824538 | GAACTGTGAGAAATA[A/T]TTTTTTTTCCTCATA | 55130 |
| rs187762126 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27899576 | CTGGCTTGAAATTCT[C/T]GCTGTGAGCATAGCA | 55130 |
| rs187762785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27881849 | CCCTGGTTTCACATT[A/G]TAATTACTTGGGGTG | 55130 |
| rs187777124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27867972 | AAAAAAAAAGCAGTA[C/T]AAAAAAGACTCCAGT | 55130 |
| rs187783421 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27846093 | AGACATCCACAGAAC[A/T]CTCCACCCCAAATCA | 55130 |
| rs187784647 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27996669 | CTGAATTTTCCAGAA[C/T]TGTAGCTACCATAAA | 55130 |
| rs187790229 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27926471 | ACCGGACAAAAATAA[A/G]CAAAATTCATATGAA | 55130 |
| rs187804336 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27895968 | AGGACCTTTTAAGAA[A/G]AAACAGCCTTGCAAA | 55130 |
| rs187819417 | snp | G/T | 1.65004e-05 | 0.00287227 | missense | ARMC4 | GRCh38.p7 | 10:27862525 | ATGTTGGTAATGGCA[G/T]CACATACACTTGCCA | 55130 |
| rs187852092 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27930912 | TTTTTGTGTTACAAT[A/C]TGGCAATCATTGTCT | 55130 |
| rs187860022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27899316 | ACGGTCTTTGCAACC[C/T]GCAGACCAGGAGATT | 55130 |
| rs187874564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27836493 | ATACTAATATGTAAA[C/T]ATATCTATACCATCT | 55130 |
| rs187880536 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27867244 | ACCCCAAAGGGCCAT[G/T]AAGTTCTCACTGGAA | 55130 |
| rs187909474 | snp | A/C | 0.00199481 | 0.0315187 | downstream-variant-500B, intron-variant | ARMC4 | GRCh38.p7 | 10:27811717 | TTGTGTGCTGAAAAC[A/C]AGTTCAGAAATTCAA | 55130 |
| rs187952276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27911926 | AACAAGACAGCCTTT[A/G]CTTACTCTTTTTCAT | 55130 |
| rs187965604 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27820019 | CATGAATGCTACTCA[C/T]GCTCATGGTGATTCT | 55130 |
| rs187974219 | snp | C/G/T | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27845491 | TGTAAAGACCATCGA[C/G/T]GCTAGGAAGAAACTG | 55130 |
| rs188036014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27976585 | CAAAACATTGGTGAG[A/G]GAATTTAACTAAGAC | 55130 |
| rs188037925 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997754 | TGGTGTTCAAAAATG[A/G]TCGGCATAACTCAAA | 55130 |
| rs188050786 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27958098 | TCATTTATAGATATA[C/T]TTTTCCTTTTATTGG | 55130 |
| rs188078479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27975058 | TGTTGTTGGCGTACA[A/G]GAATTCTGGTGATTT | 55130 |
| rs188120715 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27991972 | GATAATAAATTCTTT[C/G]GGTAATTGAGAATAT | 55130 |
| rs188124014 | snp | A/G/T | 0.00239393 | 0.0345281 | intron-variant | ARMC4 | GRCh38.p7 | 10:27947862 | CATTCTTAATCGCTC[A/G/T]TGCTGAGGACTTGCT | 55130 |
| rs188130035 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27911468 | TTTAATGGACCATTG[G/T]GAAACTACAGTCTTG | 55130 |
| rs188131042 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27823603 | TCATGCTATGTGCCC[C/G]TAAATTATAGTTGTT | 55130 |
| rs188145494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27833735 | AAATGCAGGAGTAGA[C/T]AAGAAAGGCTTGACT | 55130 |
| rs188148686 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27953529 | GTAACAAAAACTGAT[G/T]TCAGGGACAACTTAA | 55130 |
| rs188157190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27881185 | TGTTTTTTATTATTA[C/T]TTTTAGAAAGTATGT | 55130 |
| rs188160932 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27829044 | GGGATATAGAATTCA[A/T]CCCTCATGTGGATAA | 55130 |
| rs188162574 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27917736 | TGTTTTTGTTTGAAA[A/T]ACCAATTGAAAATAT | 55130 |
| rs188168921 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27885722 | ATATATATTATATAT[A/T]ATATATAAAATATAT | 55130 |
| rs188195075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27918455 | AGAAAAATCATCTGA[C/T]CATCTCAATAGATAA | 55130 |
| rs188195570 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27902623 | CAGGGGAGATCACCA[C/T]TGATCCCACAGAAAT | 55130 |
| rs188203268 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27886691 | TGCATAAAAATTATG[A/C]ATGTCAATGAGTATG | 55130 |
| rs188215744 | snp | C/G | 0.000247645 | 0.0111248 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984166 | ATAACATAAAATGAG[C/G]CTGAGAAAACATCAA | 55130 |
| rs188222060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27850226 | AAGACGGGTGAATCA[C/T]TTGAGGTCAGGAGTT | 55130 |
| rs188272586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27871383 | CATTTGTCAATTTTC[A/G]CTTTTGTTGCCATTG | 55130 |
| rs188287674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27974420 | TATGGTATAAGAAAG[C/T]GGTCCAGTTTCAATC | 55130 |
| rs188291907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27938792 | TTTAGTAGAGACGGG[A/G]TTGCACCATGTTGGC | 55130 |
| rs188303030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27840026 | TTAATAATTTACATC[A/G]ATTTAACTCACAAAG | 55130 |
| rs188303769 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27882091 | GGAGGATCACTTGAG[C/T]CCAGGAGACAGAGGT | 55130 |
| rs188307922 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27904092 | CTATGTTGACTACTC[A/C]CCAAACTGTTCCCTC | 55130 |
| rs188325583 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27846939 | ACAATTAATAGCCTA[A/C]CAACCAAAAAAATTC | 55130 |
| rs188351948 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27923961 | GAAAGAAAGAAAGAA[A/G]GAAAGAAAGAAAGAA | 55130 |
| rs188358363 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27942273 | CACCAAAAATTGGTT[A/G]AATAATTGTCTTAGT | 55130 |
| rs188362616 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27906454 | GGAAGACAGTGTGGC[A/G]GTTCCTCAAGGATCT | 55130 |
| rs188365280 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27953868 | ACGGGAAGAATACCA[C/T]GTGCTTCTGCTATGT | 55130 |
| rs188377466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27892871 | AGATGTACTACGGCC[A/G]GGTGTGGTAACTCAC | 55130 |
| rs188382696 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | ARMC4 | GRCh38.p7 | 10:27935655 | CTATTGTACCTATTT[C/G]GGTTTAATAGGTCTC | 55130 |
| rs188387233 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27875929 | GGAGGGTCCCATGCC[A/C]ACAGAGCCTCGCTCA | 55130 |
| rs188423517 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | ARMC4 | GRCh38.p7 | 10:27970943 | CACCACTGCACTCCT[G/T]CCTGGGCAACAGAGC | 55130 |
| rs188455410 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27902062 | GAATTGGAAGTAAAA[C/T]ACTCCCTAGCAAATG | 55130 |
| rs188472681 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27833041 | TGTTACCTTAAGAGA[C/T]TGGCTTTCCCCCTTG | 55130 |
| rs188526899 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27978505 | CACCAAGAAAAGGAA[A/G]ACTGGAGCCGGGCAT | 55130 |
| rs188535366 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27989567 | GACCAAATACCAAAG[A/G]TACCAAGCTACTTAA | 55130 |
| rs188539422 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27959443 | TCACAGGAGGCCCTG[G/T]GGTTCAGTAAAGATG | 55130 |
| rs188562736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27956796 | TTCTTTTTCATTATA[A/G]TGTGTATAAAATGCA | 55130 |
| rs188594034 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27961347 | CCCACTTCCCAGCCG[A/G]GAGAGAGGGTTGGTA | 55130 |
| rs188596280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27921780 | GGCAAAATAATTAGA[C/T]AAGCATCAGACTTTT | 55130 |
| rs188600633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27831271 | TGAATTGGAGGCAAC[A/G]TTTATAAAATATTAA | 55130 |
| rs188601016 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27868138 | CAATGAGGTATCATC[G/T]CATGCCAGTGAGAAT | 55130 |
| rs188608299 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27927304 | CCCAAGTTTTTACCA[C/T]AGCCACAGCCAAATC | 55130 |
| rs188609426 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27889745 | CAATTATGCATTCTC[A/G]CAGTAGAACAGTCTC | 55130 |
| rs188663670 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27871227 | TTCTTCTAAATTTGT[A/T]TGAGTTCTTTGTAGA | 55130 |
| rs188675245 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983734 | AATCTGCTTCTATCC[C/T]ACAGAATGGTAATTC | 55130 |
| rs188685950 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27945851 | CTAAAGTAGCGCATC[A/C]CACACAAAAGCAAGA | 55130 |
| rs188691804 | snp | C/T | 0.000117686 | 0.00767 | intron-variant | ARMC4 | GRCh38.p7 | 10:27961563 | CTACCATAGACCTTT[C/T]TTACCTTTAAATATT | 55130 |
| rs188694248 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27928037 | CATAGGAACCTCAAT[G/T]TCTCTACACAACCAT | 55130 |
| rs188709605 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27909886 | CCTATGACAAGAACA[C/T]GATTGAAAAACATTT | 55130 |
| rs188713479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27897324 | CTGACATCCAGATTC[A/G]TGTATTCAAATGACT | 55130 |
| rs188728676 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27879007 | AATGATACAATCGTT[A/G]TAGTCTAGACTTACA | 55130 |
| rs188739967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27995957 | CCTTTTTATCTAAAT[C/T]AGTTATCAGAAGAGT | 55130 |
| rs188744290 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27815200 | CACCATCCACTTGTA[C/T]TCTTCATTCATTCTT | 55130 |
| rs188800498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27821160 | TTTTACTTAGCTAAG[C/T]ACAGTCTCAATCAAG | 55130 |
| rs188817415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27854194 | GACATACCTGTTAGA[A/G]TGTCTAAAATCAAAA | 55130 |
| rs188843306 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ARMC4 | GRCh38.p7 | 10:27892474 | CTCATTTCACACTCC[A/G]ATTTTCCTATCAGAT | 55130 |
| rs188854323 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27875704 | ACAGTGGCTGCAGGA[C/G]AGTGGGTGCAGCCCA | 55130 |
| rs188859585 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983426 | TCATAGGGCACTGTC[G/T]CCTACCTTCTACATT | 55130 |
| rs188863218 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27857179 | CCTCCTCTTCAGCCT[A/G]CTCTACGTGAAGATG | 55130 |
| rs188873926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27837886 | CTGCATAAGGTGTAA[C/T]AAATTTGATTTTTAA | 55130 |
| rs188887628 | snp | A/C | 0.000399281 | 0.0141238 | missense | ARMC4 | GRCh38.p7 | 10:27944843 | TTCATCGGTTTCAAG[A/C]AAATTTATCAGCACT | 55130 |
| rs188904157 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27909491 | CTTAGCTATAATGAG[G/T]GAGGATTTTGATCTC | 55130 |
| rs188915016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27818398 | AAGGGTTCATGAGTC[C/T]CTGTCTTGACTCCAT | 55130 |
| rs188932017 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27987914 | CTTCATGCTTTGGGG[A/T]GTTCTAATGTTATTT | 55130 |
| rs188935448 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27885681 | ATATAAAATATATAT[A/T]ATATATAATATATAA | 55130 |
| rs188952183 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27849458 | CTAATGTAAATGACG[A/T]GTTAATGGGTGCAGC | 55130 |
| rs188959147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27948584 | TACTTATTTTCACAT[C/T]TTATCACGCATTTGC | 55130 |
| rs189019180 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27816051 | TGCCTCACACTCACT[C/T]CCACCCTCATCTCCC | 55130 |
| rs189079116 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27879481 | ATTTAAATGTCTTTC[C/T]TGCTTATACTCAGTA | 55130 |
| rs189094464 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27844099 | GCTACTGGGGAGGCC[A/G]AGGCAGACAGACCAC | 55130 |
| rs189120955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27990172 | TTTTTTTAAGAGACA[A/G]GATCTTGCTCTGTCA | 55130 |
| rs189130589 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27951894 | AGCCTGACCAATATG[A/G]TGAAACCCCATCTCT | 55130 |
| rs189140286 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27933827 | GCAACTTGTATTCCT[C/T]AGTGTCTGAAACACT | 55130 |
| rs189195977 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27878702 | AAGTGAAAACTGAAC[A/G]GGCAAATCTTGTCGT | 55130 |
| rs189200562 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ARMC4 | GRCh38.p7 | 10:27863346 | GCACTAAATGGACTG[C/T]AAAATGGACACTTGC | 55130 |
| rs189205471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27836107 | AGAGTCAGAAGGAAA[C/T]CTGCATAAAATTGGA | 55130 |
| rs189211358 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARMC4 | GRCh38.p7 | 10:27841840 | GCTCACTGCAGCCTC[A/G]ACCTCCCAGGCTAAA | 55130 |
| rs189226987 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27963878 | TCTCATTTTAATTCT[C/T]TCAACAATCTATGAG | 55130 |
| rs189233752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27931158 | AGAAAGGTTGACTAT[A/G]CTTCGAATGACCATG | 55130 |
| rs189236052 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27971499 | TAGGTGGACAGTAAC[G/T]TGATGTTCCTAAACT | 55130 |
| rs189238985 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27827002 | TATTCAAGGCCATTC[A/G]TAATCGCTTTGCTAT | 55130 |
| rs189244022 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27946432 | ATATTTTGGGGGTAC[A/G]TGTGATATTCTGATG | 55130 |
| rs189255241 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27910793 | ACAAACAAAAAAACA[A/G]ATACAGTCAATTCTC | 55130 |
| rs189274344 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27936064 | AGCCATGACTTCACT[A/G]CGCCTTATTAAGTAA | 55130 |
| rs189276448 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27954476 | CTGGCTTATAGCACA[C/T]GTTCATGAATAAACA | 55130 |
| rs189284543 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27919196 | AGTTAATCAAATGAA[A/G]AATAGTGTTTTCAAT | 55130 |
| rs189366806 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ARMC4 | GRCh38.p7 | 10:27864848 | GCATGGTACTACGCA[C/T]TTCACATAAGTTATT | 55130 |
| rs189377570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27965926 | TCCATTTAAGCCTTC[A/G]TGCTTATATCAATTC | 55130 |
| rs189388160 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27932419 | AATTTCTAAGTTGAA[C/T]GATCATAAGTTGGGA | 55130 |
| rs189412026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27900687 | AGTACCAATAGCTGA[A/G]TCGATCAGGCGGAAG | 55130 |
| rs189424185 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27838647 | TGAAAGATGGAACTG[C/T]TCTCTATAGCATCTG | 55130 |
| rs189428400 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27868924 | AAAATCATGCTCTTA[C/T]GATGAAAGCACATTA | 55130 |
| rs189460543 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARMC4 | GRCh38.p7 | 10:27972222 | TTTACTTAAAGGAGA[C/T]GTGACAAATTTGAGA | 55130 |
| rs189460994 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | ARMC4 | GRCh38.p7 | 10:27963814 | GAGTTTTTTAGACCC[C/G]CATGCATTTGGCCAC | 55130 |
| rs189464893 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ARMC4 | GRCh38.p7 | 10:27993180 | TCGGCCTTTCAAAAC[A/G]TTGGGATTACAGGTG | 55130 |
| rs189470775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27831386 | AGAGAACCTTCAAGA[A/G]GGAAAAGGACAATAG | 55130 |
| rs189509452 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27992238 | CTCTACCCTTCCAAC[A/G]TCAAAGATATCAATA | 55130 |
| rs189511555 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27961938 | AGACATGGTGGTGCA[C/T]GCCTGTAATTTCAGC | 55130 |
| rs189531692 | snp | G/T | 0.00517822 | 0.0506191 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999339 | CCCCTTTTTACATTT[G/T]TCCATAGGCTTCCAG | 55130 |
| rs189540650 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27929329 | TTGTACCATGTCTAT[G/T]GACTTTTTATGTGAA | 55130 |
| rs189555483 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARMC4 | GRCh38.p7 | 10:27897690 | AATGTTCGTGTTGCC[A/G]CAATGATAAATGCAT | 55130 |
| rs189599644 | snp | G/T | 0.00835141 | 0.0640778 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999616 | CACCTCTAGACACCC[G/T]ACCAGCAAGAGCCCC | 55130 |
| rs189603564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27933437 | TTTGTGGGCCAAGAA[A/G]ACAACATTATCAGAT | 55130 |
| rs189610052 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27952845 | GATATTTGCTTTCTG[C/T]AAGGAGCTATGAAAC | 55130 |
| rs189617150 | snp | C/T | 0.000329571 | 0.0128326 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27940680 | GATGGCTTCTTTATT[C/T]GTATGACTCTTACTG | 55130 |
| rs189617552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27900920 | GCAGAACTTCCCCAA[C/T]CTAGCAAGACAGGCC | 55130 |
| rs189618594 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27913586 | ATATGCAAACTATGC[A/T]TCTGACAAAAGTCTA | 55130 |
| rs189625729 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27883483 | TGCTTTTAACAAAAA[A/G]TGTGATACATACAAC | 55130 |
| rs189630452 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27869597 | TGGAGTGAATTGGCA[C/T]GATCTTGGCTCACTG | 55130 |
| rs189638603 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27847916 | ACTGCTCAACAAAAT[A/T]AAAGAGGATACAAAC | 55130 |
| rs189673488 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27949784 | GATGGATGCAGTCAG[A/G]TTACTGCAGGGATCC | 55130 |
| rs189680018 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27913122 | TATCATATAGTAAAT[A/G]TGTTTCTCCTTTTTT | 55130 |
| rs189694931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27858603 | TATTGCCTTTCTTTT[C/T]CTAATTCTAAAGTTT | 55130 |
| rs189700433 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | ARMC4 | GRCh38.p7 | 10:27882233 | AAAGAAAGAAAGAAA[G/T]AAATATGAACTCTCT | 55130 |
| rs189706043 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27954910 | TCACTTCTTATACTA[C/T]AATATCTATGAAAGC | 55130 |
| rs189739219 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27919740 | AGTAAAGTTAAACAC[A/G]TACTCTGTGATGACT | 55130 |
| rs189739650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27972646 | AAAATCAGACAATAT[C/T]GACTCCAAAGCAAAT | 55130 |
| rs189754341 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27955667 | TACAACTTCCAATTA[C/T]CACTCGAAAGAACTC | 55130 |
| rs189755179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27887079 | CATTGGCAAAATGGA[C/T]TTTAAAAAAACAATT | 55130 |
| rs189767522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27920201 | TCTATTTCTTGACTT[A/G]GATGGCAGTTACATA | 55130 |
| rs189769716 | snp | C/T | 1.64768e-05 | 0.00287021 | synonymous-codon, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27936737 | TTACTTGGTAACATT[C/T]TCTTTGCTGATGGAA | 55130 |
| rs189785013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27828026 | GGAGGCCATGAAATC[A/G]TAGAAACCAGTGAAA | 55130 |
| rs189785963 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27903461 | CCGGGGCAATCAGGC[A/G]AGAGAAAGCAATAAA | 55130 |
| rs189786862 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27864387 | ATCTAGGATGCAGAT[C/G]AATGTATGGGCTTGG | 55130 |
| rs189788029 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27888000 | CATGAAGAAACAGAA[A/C]ATCTGAACAGATCAG | 55130 |
| rs189796765 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872985 | TGAATCCCTCTGATC[C/T]TGGACTTATTTTGGT | 55130 |
| rs189807154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27853981 | ACGGGGAGAAAATAT[C/T]TGCAAATTACACATA | 55130 |
| rs189827197 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | ARMC4 | GRCh38.p7 | 10:27812212 | TCGCCACAAATACAA[A/C]AGCATCACTGAACTA | 55130 |
| rs189930293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27870856 | ATGATTCATAATCCT[C/T]TGGGTATATACCCAG | 55130 |
| rs189938586 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27848447 | TAAAGACCTAAAACC[A/G]TACAAACCCTAGAGG | 55130 |
| rs189967459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27972368 | GGAAGGAAAAAAACT[A/G]CAAAGAACAGATGAA | 55130 |
| rs189971759 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27936481 | CTGCCCATATGCAAA[A/T]TAGAGAAATCATGTC | 55130 |
| rs189988029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27903251 | ATAAAATTCAACACT[C/T]ATTCATGCTAAAAAC | 55130 |
| rs190038528 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27977993 | AACATACAACTACCA[A/T]ATGATCTTACCATTT | 55130 |
| rs190062890 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27813954 | ATGGCCCCAGAACAA[A/C]TGCTTATCCAAATAG | 55130 |
| rs190069324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27832078 | GGGGCTAACACAGAG[A/G]TAACTCAATAAACAG | 55130 |
| rs190074077 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | ARMC4 | GRCh38.p7 | 10:27941338 | GAAAAAAAAAAAAAA[A/C]GCTGGATGTGGTGGT | 55130 |
| rs190084053 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27906017 | CCAGAATTGACAAAT[A/G]GGATTGAATTAAACT | 55130 |
| rs190086524 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27830452 | GAGTTTTATGTGGCT[C/G]ATAGATAGCCTTGCT | 55130 |
| rs190113503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27817445 | TTAATGCACCCACCA[C/T]CCATATAGTGAACAC | 55130 |
| rs190119952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27835622 | AATAACATAAACAGT[C/T]GATCAACACCTAGTT | 55130 |
| rs190190907 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27982009 | TGTTTGTCACACTCT[A/G]TTCTTCTGTCTGTGG | 55130 |
| rs190201131 | snp | C/T | 3.42841e-05 | 0.00414016 | synonymous-codon, intron-variant | ARMC4 | GRCh38.p7 | 10:27944252 | CCCGTGCTGCCTCAC[C/T]ACCCGCCGTGCTCTT | 55130 |
| rs190207365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27960602 | CGATCCACCCTCCTC[A/G]GCCTCCCAAAGTGCT | 55130 |
| rs190209299 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27926082 | TCTGTAAAGAGCTAG[A/T]TATTATTTTAGTCTT | 55130 |
| rs190213883 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ARMC4 | GRCh38.p7 | 10:27902833 | CCAAAAAAAGCCCAG[A/G]ATCAGATGGACTCAC | 55130 |
| rs190223662 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27908085 | CTAAATGTAAAAATA[C/T]GGGTTTCTTTCATAT | 55130 |
| rs190236247 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872445 | TGCCAGTTTTCAAAG[G/T]GAATGCTTCCAGTTT | 55130 |
| rs190279208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27853046 | TCCCCTCCCAATAAA[A/G]GCAGAGGTTGTATAA | 55130 |
| rs190305004 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27998209 | AGTCCGCGCATACAC[G/T]GCTTTCTGAGAATGC | 55130 |
| rs190306738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27958690 | AGAAATGATTATTAT[C/T]GCCAACAGTTACTAA | 55130 |
| rs190322402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27834356 | CCTTGGCCTTCTGGA[A/G]TAGACATACAACCCG | 55130 |
| rs190331465 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27923057 | GCAAACCTTTCTAAA[C/G]AACAACAAATTAAAG | 55130 |
| rs190344770 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27947819 | CCTGCCCCAGGTCTA[C/T]GCAGTGAAGAAGACT | 55130 |
| rs190367327 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27930012 | GAGGAATACCAATTA[A/C]GTTTATGTTGGCTCT | 55130 |
| rs190375885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27911055 | TTGTGCCTGAATGGC[A/G]TTTAGGGAATACACA | 55130 |
| rs190377706 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27899160 | ACAGCCCACGGAGGG[C/G]AAGCAGAAGCAGACT | 55130 |
| rs190388918 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27856963 | CAAGACCGAAACTCC[A/G]TCCCAAAAATAAATA | 55130 |
| rs190476482 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27886885 | AACCATAAAATATAC[A/G]CAAAAGGATATCAAA | 55130 |
| rs190490676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27851343 | CTTAGAACAAAGCTC[A/G]GGAATATTTATAGAT | 55130 |
| rs190504659 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27989821 | ACCACTGCACTCCAA[C/T]CTGAGTGACAGAGTG | 55130 |
| rs190512462 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27951471 | GACTGCAGAATTTGA[G/T]GAAGGTGGTATCCCA | 55130 |
| rs190528266 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27963303 | TGAGCCACTGCACCC[A/G]GCCTGTCCCAGGCAC | 55130 |
| rs190534533 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27986416 | TATATAGAAATCTAC[A/G]TATTATGTCTACCAA | 55130 |
| rs190534738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27823352 | AGATCAAAGTGTAGA[C/T]GGCAATTCTCTGGAA | 55130 |
| rs190560002 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27922728 | CTGGTCAAAATGTTG[A/G]AACCCTGTCTCTACT | 55130 |
| rs190561210 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27816315 | AATAAGACAGGATCA[A/G]TCTTCTGAGATTCAA | 55130 |
| rs190564742 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ARMC4 | GRCh38.p7 | 10:27820587 | GTACCCTTTTTATGA[C/T]TCTATTCTATAAATT | 55130 |
| rs190569152 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27891345 | TTGGAGCAGAACTTT[A/G]GGTCACTGGTTTTCA | 55130 |
| rs190603591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27985460 | TCCCTAATAGCACAA[A/G]GACCAAGACAGTCAT | 55130 |
| rs190649161 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27837340 | AGGTTTTTGTTTTTA[C/T]TTCTCTGTATGCAAA | 55130 |
| rs190667884 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27991443 | TAAAACCTTTCCAGT[A/G]TGTGACTAAAGTATC | 55130 |
| rs190670262 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27817768 | TTGATTCCATATCTT[G/T]GCTATTGTGAATAGT | 55130 |
| rs190696583 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27907309 | CAGTCATGTCTCCCC[C/G]ATGGCTGCACTCTCT | 55130 |
| rs190698674 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27893656 | TGTAGAAATGCTTCC[A/G]TACAAAATAAAAGGC | 55130 |
| rs190702741 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27913801 | CTATCTCACATGAGT[C/T]GGAATGGCTATTATG | 55130 |
| rs190713267 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27877567 | ATTTTAAACATATGA[C/T]GTCTTGCCTCGCATA | 55130 |
| rs190726437 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27839543 | CGTATAGCTGACAGT[C/G]ACTTGGAAATATTAT | 55130 |
| rs190757635 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27906764 | AAACTAATACAGGAA[A/C]AAAAAACCAAACACC | 55130 |
| rs190771985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27966534 | GCTTTTCCTATTTGA[C/T]ATGATTTCTTCCAAT | 55130 |
| rs190784347 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27987720 | CACTCAAACTCTTAA[A/G]TCCTCAAACTTACCA | 55130 |
| rs190815571 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27905552 | AAAAAAGAGCCTGTA[C/T]AGCCAAGACAATCTT | 55130 |
| rs190818049 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27947979 | GTTTTCTTAATTTTT[C/T]TCTTCTAGACAACTT | 55130 |
| rs190820177 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27911539 | TGCAATAGATGTGAG[C/T]GTGGAGTTTCACATG | 55130 |
| rs190827383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27995739 | CTGAGTTAAAAAAGA[A/G]ATAGAATAAGAACAG | 55130 |
| rs190831896 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27813102 | TTAACTAGTCCTTGA[A/T]GGGTTTGTGCACTCT | 55130 |
| rs190846315 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27881266 | TGAAATTTATTTGAT[C/T]CCACATGTCATTAAC | 55130 |
| rs190849940 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27974178 | ATGCTGGATATTAAA[A/C]CTTTGTCAGATGCAC | 55130 |
| rs190851311 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27898155 | TAAATTTGACATTTA[A/C]ATATAGATTTTCAAT | 55130 |
| rs190853742 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27879939 | TACTCTCTCATTTAT[C/T]GAAGTTCCTCTGAAA | 55130 |
| rs190866137 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27956485 | GATATCCAACTGTGC[A/T]TGCCAATATAACCCT | 55130 |
| rs190867269 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27865361 | GAATTAGTCCTTCAG[G/T]TTTCATGTCCTCAAA | 55130 |
| rs190874153 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27844588 | CTGGGTGATTTGGGG[A/C]AAGTTATTTAATCTT | 55130 |
| rs190913086 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | ARMC4 | GRCh38.p7 | 10:27969999 | TAATCCCAGCTACTC[A/G]GGAGGCTGAAGCAAG | 55130 |
| rs190928402 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, missense | ARMC4 | GRCh38.p7 | 10:27836024 | TCTTCATCCTCGTCA[C/T]CTTCCCGTTGAGTAG | 55130 |
| rs190981707 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27901412 | TATATCAACTAATGG[G/T]CAAAATAACCAGCTA | 55130 |
| rs190983945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27829315 | AGATGAAAATAAATG[A/G]CTAATTTCTTGGGAA | 55130 |
| rs190991617 | snp | A/C | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27960089 | AAGTATCACGCTTAA[A/C]ATGAAATTTTAAAAC | 55130 |
| rs190996319 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27934498 | CTCTCTATATGTATA[C/T]TGTATCTTTTTGTTC | 55130 |
| rs190997541 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27979140 | ACTTGAACCCGGGAG[C/G]GGAGGTGAAGGTTGC | 55130 |
| rs191007639 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27916174 | GTGTGAAAGAAAGTG[C/T]CAATATAGTAGAGCA | 55130 |
| rs191007732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27901746 | GTAAAGGGATCAATG[C/T]AACAAGAAGAGCTAA | 55130 |
| rs191014044 | snp | A/G | 0.030278 | 0.119257 | intron-variant | ARMC4 | GRCh38.p7 | 10:27885278 | GCACTTTGGGAGGTC[A/G]AGGTGGGCAGATCAC | 55130 |
| rs191024170 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27871116 | GCCACTGATGATGAG[C/T]ATTTTTTCGTGTGTC | 55130 |
| rs191035808 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27848640 | CTACAGAATGGGAGA[A/C]AATTTTTGCAATCTA | 55130 |
| rs191045530 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ARMC4 | GRCh38.p7 | 10:27963714 | AGAAATGCTCATGTT[C/T]TTGATTACAGGGTAT | 55130 |
| rs191052399 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27822914 | CCATGTTTCTTCACG[A/C]ACTTTCCACTAGAGA | 55130 |
| rs191057685 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27930946 | ATACCCTTTTCACTC[C/T]GAAATGTCTACGAAA | 55130 |
| rs191068029 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27995231 | TCCACCTTTTCCTTG[G/T]AACATTTTTCATTCT | 55130 |
| rs191081156 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27899346 | TCCCTCAGGCGCCCA[C/T]ACCACCAAAGCCATG | 55130 |
| rs191103350 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27867752 | GTCAGGAGGTTGAGA[A/C]CAGCCTGGCCAACAA | 55130 |
| rs191154481 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27969359 | TCTTCCCCACCCAAC[A/G]TTGCAACAGGGCCTG | 55130 |
| rs191162050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27933990 | TTGTGGGAGAGACCC[A/G]GTGGGAGTTAATTGA | 55130 |
| rs191216130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27829702 | TAATAAGCAACTAGA[C/T]ATTAATTTGTCTTTT | 55130 |
| rs191235658 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27884905 | GCTTTTACTCTGGGA[C/T]GATCCCAGGCTCAGA | 55130 |
| rs191266943 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARMC4 | GRCh38.p7 | 10:27971656 | AAAGATAAAGGGAAC[A/G]TCTTGAAGGTAGACA | 55130 |
| rs191280611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27953936 | GCCACACCCACTCAG[A/G]GAGCAAGAGCTGGGA | 55130 |
| rs191294808 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27918874 | TTGAATATACAAAGG[C/T]ATATTCAAAAATTAA | 55130 |
| rs191297467 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27935799 | TCTGATATATATGTA[C/T]ATATGTATGTGTGCA | 55130 |
| rs191302081 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27982939 | CTCACGCAGGAATCT[A/G]CAATGTCGTATTTCT | 55130 |
| rs191313163 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27902760 | CAGGAAGAAATCAAA[C/T]CACTGAATAGACCAA | 55130 |
| rs191316916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27886711 | CAATGAGTATGCAAT[A/G]TATAAAGATGTTATT | 55130 |
| rs191334003 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27866854 | CTCCTCCCATTAGAC[C/T]CCACTCCAACACTGG | 55130 |
| rs191361802 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27845808 | TTTTAAACCAACAAA[A/T]ATCAAAAGAGACAAA | 55130 |
| rs191376356 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27991143 | GTTTCATTCTGAGGT[A/G]TTTTAGGAAGACTAT | 55130 |
| rs191390569 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27829864 | AGAGCCCATCTTACA[C/T]GATTTTTGCCAACTT | 55130 |
| rs191421229 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27914708 | TATATATGTGTGTGT[A/G]TATAAATATGCATGT | 55130 |
| rs191435190 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27957575 | GAATTAGGGTACAGC[A/G]TCATCACCTATGGGG | 55130 |
| rs191435477 | snp | C/T | | | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27996027 | TTCACATTGGCTAAA[C/T]AGAAATTAGTCTGTA | 55130 |
| rs191443155 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ARMC4 | GRCh38.p7 | 10:27922066 | CAGGCACTTGGTAGG[C/T]TGAGGTGGAAGGATA | 55130 |
| rs191448344 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27864546 | GTGAGGTGAGAGCGG[A/G]GAGTGAGGTGAGAGC | 55130 |
| rs191449244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940360 | AGTATATATGTGTGA[A/G]ATATATATATATACA | 55130 |
| rs191453532 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | ARMC4 | GRCh38.p7 | 10:27904721 | CCAGTTTTTCCCTGG[A/C]TATTCCGACATGTTT | 55130 |
| rs191454061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27813562 | TTTAAAAGTAAATTT[A/G]AATCACATATTTTTT | 55130 |
| rs191471252 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27890992 | ATACAGCGATATATT[C/T]GACAGCCCAAACATG | 55130 |
| rs191475661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27875148 | CCAGTTGATTGAATC[A/G]GCTACTAAAGCTTGT | 55130 |
| rs191491064 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27848242 | TAGACAAATGAAAGA[G/T]AACAGAGCCCTCAGA | 55130 |
| rs191562681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27880336 | TATCTGGATGTCTTC[C/T]TGAAGTAAATAATTT | 55130 |
| rs191583570 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | ARMC4 | GRCh38.p7 | 10:27845065 | GGAAATACAGAGAAC[A/G]CCACAAAGATACTCC | 55130 |
| rs191594899 | snp | A/C/G/T | 6.60382e-05 | 0.00574585 | missense, utr-variant-5-prime, intron-variant | ARMC4 | GRCh38.p7 | 10:27981558 | TTCTCTCATAATTAA[A/C/G/T]GTCCCCTTCATCATC | 55130 |
| rs191608798 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27975748 | CAAACAATATTAATT[A/C]TATACAAACTCTTCC | 55130 |
| rs191614962 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27996685 | TGTAGCTACCATAAA[C/T]GAAAAGAAGGTTGTA | 55130 |
| rs191616658 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27833434 | ACGGAAAATACAGCA[C/T]TGGAAATAAAATGCA | 55130 |
| rs191626556 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27943656 | GCCGGGCTTGATGGC[A/G]GGCACCTGTAGTCTC | 55130 |
| rs191676787 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27884311 | AAATAAACAACTACA[C/G]ACTGACTCAATTTTA | 55130 |
| rs191718160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27831880 | GGTATATGTGGCTCC[C/T]CTCTCCCCTGCATGC | 55130 |
| rs191722061 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARMC4 | GRCh38.p7 | 10:27974494 | TAGGGAGTCTTTTCC[C/T]CATTGCTTGTTTTTG | 55130 |
| rs191764625 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ARMC4 | GRCh38.p7 | 10:27871566 | TCCAGTTTCACCTTT[C/T]TACATATGGCTAGCC | 55130 |
| rs191768104 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27895459 | AGCCTAGCTAATTTT[G/T]GTATTTTTAGTAGAG | 55130 |
| rs191771794 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27850005 | AAGTTCCATGAGTCA[A/C]GGTTTGAAATCTACT | 55130 |
| rs191775848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27815620 | ACTGGCTTCTTCTAC[C/T]GTACTCCCCTGCTTT | 55130 |
| rs191793790 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27874440 | AGTTGATGCAGTTTC[C/T]TCCTAGCATCGATGG | 55130 |
| rs191861353 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:28000294 | GAAAGTGCGAAAGTT[A/G]TTAGGAATGGAATAG | 55130 |
| rs191880159 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27890259 | GGTCCCAGTCAGGTG[C/T]CTGAGTCAATGAATT | 55130 |
| rs191881777 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27874715 | TGTAGGGTTTCTGCC[A/G]AGAGATCCACTGTTA | 55130 |
| rs191890762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27855369 | ATCAGAAACAAGTCT[A/G]TTTATTACTCTATAT | 55130 |
| rs191897454 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27836439 | TATCAGTTTTCTAAA[C/T]TTGATCAATGAGAGA | 55130 |
| rs191919633 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27925939 | TGAGCCCGGGATGCA[A/G]GGGTTGCAGTGAGCC | 55130 |
| rs191933115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27965311 | CCCTGTGGTTACACA[A/G]AGCCTAGGGAAAAGA | 55130 |
| rs191940795 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARMC4 | GRCh38.p7 | 10:27938660 | GCTGAAGTCCAGTGG[C/T]GCGATCTTGGCTCAC | 55130 |
| rs191942167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27988617 | TACTGGGATTACAGG[C/T]GTGAGCTACCACACC | 55130 |
| rs191945394 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27836179 | TATATATTCAGTACA[A/T]ATACACAGTTGAATA | 55130 |
| rs191950224 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27962716 | ATATATGCCCTACGT[C/T]CCTGCAGAGGTCCCT | 55130 |
| rs191953646 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27949639 | TGAAAACCAGCTGGG[C/G]TGCTGGGCCCAGAGT | 55130 |
| rs191957651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27929670 | ACGAATATGATATTG[C/T]CTTCACATTTGAAGG | 55130 |
| rs191958028 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27903675 | CAAAGAGAGAGCCAA[A/G]TCATGAGTGAACTCT | 55130 |
| rs191964900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27932083 | AGGACTACAGGCGCA[C/T]ACCCTCACATCCTTT | 55130 |
| rs191967802 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27901117 | AACAGTGGATCTCTC[G/T]GCAAAAACTCTACAA | 55130 |
| rs191976413 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27870597 | CCTATGAGTGAGAAT[A/T]TGCGGTGTTTGGTTT | 55130 |
| rs191998955 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARMC4 | GRCh38.p7 | 10:27832658 | GTTAGCACATTTCAT[A/G]AATTACCAGAGCACA | 55130 |
| rs192071154 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27924462 | AGAAAAATAGCTACA[A/C]TATAAACCAAAAGAG | 55130 |
| rs192086369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27893255 | AGAAGCAATATTCAC[A/G]TCTTATTTTCTTAAC | 55130 |
| rs192098908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27927548 | TTTTCTGAAACTTAG[C/T]GTATTTATAAAAACA | 55130 |
| rs192101263 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27860035 | GTACTACTGCTTGTC[C/G]ATATGCTGTACATTT | 55130 |
| rs192102319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27970549 | TCTTCTCTTCCCTTC[A/G]CAGTGCTCCACACAT | 55130 |
| rs192103013 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27854666 | GAGGCTGAGGCATGA[A/G/T]AATTGCTTGAGCCAA | 55130 |
| rs192108045 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | ARMC4 | GRCh38.p7 | 10:27909617 | GAGGTCAGGAGTTCA[A/T]GACCAGCCTGGCCAA | 55130 |
| rs192114367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27953181 | AACACTTAATCTGAG[A/G]TTTACTTCTTAAATG | 55130 |
| rs192124454 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27896768 | GATATATGTATATAG[A/G]TATAGATATATAGAT | 55130 |
| rs192128480 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27878704 | GTGAAAACTGAACGG[A/G]CAAATCTTGTCGTCA | 55130 |
| rs192128600 | snp | A/G/T | 8.27306e-05 | 0.00643112 | intron-variant | ARMC4 | GRCh38.p7 | 10:27934980 | TCCCTAACACTTATA[A/G/T]AAAATCTTTCCATCT | 55130 |
| rs192142577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27863886 | ATGGGAGAAAGTGAG[A/G]CTTAAGAGGTGAGAT | 55130 |
| rs192149485 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27842154 | TCATTTGACCCCCTT[A/T]GTTTCCTTTACAGCA | 55130 |
| rs192161298 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | ARMC4 | GRCh38.p7 | 10:27992631 | GGAGTTTGAGCTGCA[C/G]TGAGCTATGATCACT | 55130 |
| rs192192847 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27960832 | TGAGTTAAGTCAAAT[A/G]CTTTTTCACAAATAC | 55130 |
| rs192220343 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27926556 | TTTCTGAAATGTACT[A/C]TGACTATGTAAGATG | 55130 |
| rs192237388 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27827144 | AACACTTTCCTGATT[A/G]TTTGTTAGTATTTTC | 55130 |
| rs192256454 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27818607 | TCCATACGCAAATGA[A/G]ATTTAGAAAAAAATC | 55130 |
| rs192266425 | snp | A/T | 0.0356815 | 0.128715 | intron-variant | ARMC4 | GRCh38.p7 | 10:27921609 | AAATGGATTTTTTTT[A/T]AAAAAAAGGAGGAAT | 55130 |
| rs192286996 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27991819 | GGCCTTACACATGGA[C/T]GCCCAGACCTGAGTC | 55130 |
| rs192287760 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27947131 | AGGAGAAAAGTTACC[A/G]CCACCAATACCACCA | 55130 |
| rs192287939 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27888717 | CCACAATATATCCAC[A/G]TAACAAAACTGTACA | 55130 |
| rs192298876 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ARMC4 | GRCh38.p7 | 10:27846188 | GTAAAGCACTCCTCA[A/G]CAAATGTAAAAGAAC | 55130 |
| rs192325255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27814360 | GGACCCCTTCCCACC[C/T]GGCTGTCTCAATGAG | 55130 |
| rs192378253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27856836 | GTCGGGCATCATGGC[A/G]GGTGCCTGTAATCCC | 55130 |
| rs192416705 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27943375 | GTGTTTATTTCTAGT[A/G]GTTTTTTTTAAAGAT | 55130 |
| rs192437502 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27948593 | TCACATTTTATCACG[C/T]ATTTGCATTTCTGAG | 55130 |
| rs192447679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27931732 | AATGCAATGATAACA[C/T]TTAGAAGGAATTTCA | 55130 |
| rs192449422 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ARMC4 | GRCh38.p7 | 10:27907114 | GAAATAGGCTCAAAA[A/G]TGATCTTCAAAGAAA | 55130 |
| rs192457935 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997870 | AATCCATGTAAATAC[A/T]CAGCACACACCTTTG | 55130 |
| rs192459144 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27876868 | CTAATCCTAAAATCT[A/G]ATGTGGTCATTCACA | 55130 |
| rs192459384 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27976765 | TAATATTCTTATGGA[C/T]ATGCAAAAGATCTAG | 55130 |
| rs192463671 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ARMC4 | GRCh38.p7 | 10:27899704 | AGCCTCCAGGAAGTT[C/T]GAACTGGGCGGAGCC | 55130 |
| rs192466286 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27912217 | CTTGCTCTGAATTCA[G/T]TTCCAGCAGTATGGT | 55130 |
| rs192479977 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27881973 | AAGTTCGAGACCAGA[C/T]TCGACAACATGGTGA | 55130 |
| rs192483184 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27838989 | TTATGCCAATCTAAC[A/G]CTTTTGATATCCAAA | 55130 |
| rs192484493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27830212 | ACCTCCTGGTTTCCC[A/G]GAATGTCTTTCTCAC | 55130 |
| rs192484770 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27867995 | ACTCCAGTCAATTTC[C/T]ATATACAGTTATTAT | 55130 |
| rs192489379 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27989660 | TACCAGTTGAAGCCT[A/G]TAACTTAACAGAGAA | 55130 |
| rs192518006 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27949933 | CTCCAACTCTGTTGG[A/G]CAACACGCTTGCAGG | 55130 |
| rs192537668 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27840600 | TGAAAATGGGGGTGG[A/G]GAAAATATGTGGCCT | 55130 |
| rs192560645 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27824674 | ATTTGAAACAATCCA[C/T]AGGTTTCCTCCAGAC | 55130 |
| rs192613379 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944511 | AGTATACCTAAAATC[A/C]TTCCCCAGTTAAGTT | 55130 |
| rs192626834 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27909251 | GTGATATTTAACTGT[A/G]TATTGCTGGACAGAA | 55130 |
| rs192637722 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ARMC4 | GRCh38.p7 | 10:27841647 | GTGATCTGCCTGCCT[C/T]GGCCTCCCAAACTGC | 55130 |
| rs192656340 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27971409 | TCAGGAAAGGAAGTC[C/T]CGGATGCATTTAACT | 55130 |
| rs192682633 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ARMC4 | GRCh38.p7 | 10:27902220 | TACTGGGTAAATAAC[A/G]AAATTAAGGCAGAAA | 55130 |
| rs192705062 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27878149 | AGATCATTCCCTAAG[A/G]CAAACAAAAACAGTC | 55130 |
| rs192740079 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27830621 | TTAGGAAGGTCTCCA[C/T]TGGGGGCCCCCTAAA | 55130 |
| rs192748685 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27836506 | AACATATCTATACCA[C/T]CTAAAATGATTTTTT | 55130 |
| rs192758850 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27921891 | AGAACTTTAGGCCGG[A/G]CGCCTTGGCTCATGC | 55130 |
| rs192759774 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27868687 | GGCCTGCTGGGGCAC[A/G]GAGGGAGGGAGAGCA | 55130 |
| rs192807022 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27965980 | CCCTCCTCTGCTCTC[C/T]TCAACTCCCAGTGGG | 55130 |
| rs192817616 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27862065 | AGCTTGCTAAACTGG[G/T]GAGGCACATTTGATT | 55130 |
| rs192844182 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | ARMC4 | GRCh38.p7 | 10:27956866 | CTCTACTGAAGAATA[A/C]CCATTTGCATGAATT | 55130 |
| rs192854062 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ARMC4 | GRCh38.p7 | 10:27900279 | GCATCAACATCAACA[A/G]AAAGGACGTCCACAA | 55130 |
| rs192873000 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27991993 | TTGAGAATATCTCTG[A/G]TTGACATCACTTGTT | 55130 |
| rs192877182 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27953619 | ATGTAGTCATTAAAA[G/T]GAGTGAGGCAGATAT | 55130 |
| rs192877934 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27943710 | GAAAATTGCTTGAAC[A/G]CTTGAACCCCGTAGG | 55130 |
| rs192894064 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27917813 | CCCAAAAAAGAGACT[A/G]ATGGAGAGAGAGAAA | 55130 |
| rs192902699 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27824347 | AATAAGACCTGAGGG[C/T]TCTGCCCTTATGAAC | 55130 |
| rs192907288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27945410 | GTGCAGGAAGCAGCA[C/T]CGCAATCCATACTGG | 55130 |
| rs192929737 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27885689 | TATATATAATATATA[A/T]TATATAATATATATA | 55130 |
| rs192937887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27849490 | CACCAGCATGGCACA[C/T]GTACACATAGGTAAA | 55130 |
| rs192942472 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | ARMC4 | GRCh38.p7 | 10:27812218 | CAAATACAAAAGCAT[C/G]ACTGAACTAAAAATA | 55130 |
| rs192960396 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27815308 | CCATTATCATTTAAA[C/G]ACGTCTTACACATTA | 55130 |
| rs192962189 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27882209 | AAAGAAAGAAAGAAA[A/G]AAAGAAAGAAAGAAA | 55130 |
| rs192966269 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ARMC4 | GRCh38.p7 | 10:27904158 | CAGCTCTGTAAGCAT[A/G]AATGACTTAGAAATT | 55130 |
| rs192972334 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27846967 | TTCCAGGATCAGATG[C/G]ATTCACAGCCAAATT | 55130 |
| rs192992055 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983481 | TGTCCCTCCAACTCT[A/T]AGGATGCAAGCTGCA | 55130 |
| rs193050414 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27912466 | TTCTCAGGCTCTTGT[A/T]ATGTTAACATTTTCC | 55130 |
| rs193058189 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27939415 | ATGAAAATCCAATGG[A/T]GTTCTTGTTAAAAAT | 55130 |
| rs193065583 | snp | C/G | 0.000512748 | 0.0160046 | missense | ARMC4 | GRCh38.p7 | 10:27940723 | GCCAGTGCCCCACAG[C/G]GAGCCACTTCCACGT | 55130 |
| rs193076876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27963908 | GGTTGTCATTACTCT[C/T]ATTATAGAGATAATG | 55130 |
| rs193079999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27905588 | AAAAGAACAAGGCTG[A/G]AGGCATCACACTACC | 55130 |
| rs193085148 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ARMC4 | GRCh38.p7 | 10:27875631 | GAGTGATGCAGAAGA[C/T]AGGTGATTTCTGCAT | 55130 |
| rs193092442 | snp | A/G | 0.00358779 | 0.0422022 | downstream-variant-500B, intron-variant | ARMC4 | GRCh38.p7 | 10:27812063 | TGGAACTCTCCCGTG[A/G]GTTGCAAGTGATCAA | 55130 |
| rs193092983 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | ARMC4 | GRCh38.p7 | 10:27837790 | AATGAACACAGCATC[C/T]GCAAGCCCTGACTTG | 55130 |
| rs193127355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27896161 | TCATGAATTTAGCCA[C/T]AAAGATTTACTTTCT | 55130 |
| rs193130945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27862762 | ATTTATTTCTATATT[A/G]TATATTATTTCTACA | 55130 |
| rs193164217 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | ARMC4 | GRCh38.p7 | 10:27901976 | AGACATCTACATAAC[C/T]CTCCACCCCAGATCA | 55130 |
| rs193170263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27871276 | TGTCAGATGAGTAGA[C/T]TGCAAAAATTGTCTC | 55130 |
| rs193185051 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27833125 | TAGTTCAATTTACTC[C/T]GAACCCCAGCTATAT | 55130 |
| rs193203302 | snp | C/G/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27961371 | GTTGGTACCAGGCAG[C/G/T]CTGGTTGCTCCATGA | 55130 |
| rs193232653 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27958276 | GTACTGGGACAGAAA[C/T]AGTGCATCTCTTTTT | 55130 |
| rs193236724 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27987968 | AGTAATTAGTGGTTA[G/T]GGGTTTTCTTGGCTA | 55130 |
| rs193240469 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27922765 | ACAAAAATTAGCTAG[A/G]CATAGTGGTGCATGC | 55130 |
| rs193242966 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27891894 | TATCTTAATGTTCAC[A/C/G]GAGCACAAATTTGAG | 55130 |
| rs193248025 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27856988 | TAAATAAATAATAAT[A/G]ATATAAAGTATCTTA | 55130 |
| rs193281300 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27878619 | AGTATTTGAAAAAGA[A/T]TTTAAAATAGCACAT | 55130 |
| rs199511486 | snp | A/C | | | missense | ARMC4 | GRCh38.p7 | 10:27995026 | TTTATAGATAAAACT[A/C]TCCACAAACACAATA | 55130 |
| rs199551566 | snp | A/G | 0.00199792 | 0.0315431 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940535 | AGTCAAGTTGAGAAG[A/G]CAAGGGAAGCAGAAC | 55130 |
| rs199570908 | in-del | -/TC | 0.00914312 | 0.0669923 | intron-variant | ARMC4 | GRCh38.p7 | 10:27848808 | ACGAGAAAATGCTCA[-/TC]ATCACTGGCCATCAG | 55130 |
| rs199591693 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27981339 | GTTATGTTATGTTGT[-/A]AAAAAAAAACCACTA | 55130 |
| rs199595892 | in-del | -/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27938604 | TGTCTCTTCTTTTTT[-/C]TTTTTTTTTTCTCTT | 55130 |
| rs199608065 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27962819 | GTCACCAAATCCACA[A/G]TGATGTCTCAGGAAC | 55130 |
| rs199625323 | in-del | -/T | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27959376 | CTCCACTGCCAGTTC[-/T]TTTTTTTCTTTCCCC | 55130 |
| rs199629412 | in-del | -/C | 0.0170251 | 0.090679 | intron-variant | ARMC4 | GRCh38.p7 | 10:27875409 | GAGAGGAGCTGCGTT[-/C]CTTTGGAGGGGGAGA | 55130 |
| rs199639106 | in-del | -/CTCT | 0.0126979 | 0.078662 | intron-variant | ARMC4 | GRCh38.p7 | 10:27918516 | TTTATTAAAATATAA[-/CTCT]CACAGCAAACTAGGA | 55130 |
| rs199651496 | in-del | -/TG | 0.0197687 | 0.0974348 | intron-variant | ARMC4 | GRCh38.p7 | 10:27998450 | AGCGGGAGGCAGAGC[-/TG]CAAAGGGCGGAGGAG | 55130 |
| rs199652327 | snp | A/G | 6.59761e-05 | 0.00574314 | synonymous-codon, intron-variant | ARMC4 | GRCh38.p7 | 10:27971140 | GGTCTTCCAGTTTAA[A/G]CTTGGTTCCCATCTC | 55130 |
| rs199682186 | in-del | -/CG | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27945004 | TTAAGGAACACCGCA[-/CG]TTCCCATAGAAATGC | 55130 |
| rs199682573 | in-del | -/CT | | | utr-variant-3-prime, intron-variant | ARMC4 | GRCh38.p7 | 10:27812184 | TGGGAAGGCCATATC[-/CT]TTTTATTAAAATCGC | 55130 |
| rs199711346 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27895036 | GACTCACTAGTCATC[A/G]GTACGAAAAAAAAAA | 55130 |
| rs199713909 | snp | G/T | | | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:28000904 | GATTTATCATGACTT[G/T]TTTTTTTTTTTTCTT | 55130 |
| rs199728791 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27855202 | AGATCTCTTAAAATT[-/A]AAAAAAAAATTGAAA | 55130 |
| rs199758495 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27842402 | TCTGGATAGACACTA[-/A]GCATACATGATCATT | 55130 |
| rs199761489 | in-del | -/AA | 0.0244538 | 0.107838 | intron-variant | ARMC4 | GRCh38.p7 | 10:27830765 | TGATGGAGATTCAAT[-/AA]AGTCATTCCTTCAAT | 55130 |
| rs199776339 | snp | C/T | 0.000235251 | 0.010843 | intron-variant | ARMC4 | GRCh38.p7 | 10:27961564 | TACCATAGACCTTTC[C/T]TACCTTTAAATATTT | 55130 |
| rs199793409 | snp | C/T | 0.000442813 | 0.0148731 | intron-variant, utr-variant-3-prime | ARMC4 | GRCh38.p7 | 10:27939866 | CTATGTGAGAAAGAA[C/T]GCCAACAACCGCTGG | 55130 |
| rs199821545 | in-del | -/A | 0.339882 | 0.233284 | intron-variant | ARMC4 | GRCh38.p7 | 10:27918909 | GTATCCATTACTTGT[-/A]AAAAAAAAAACTGGA | 55130 |
| rs199836959 | snp | A/G | 0.00014844 | 0.00861383 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27944346 | TCAAGTATATTCACC[A/G]TAATTGGTAAGCCCC | 55130 |
| rs199866722 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27859057 | AAATTTTATAGTTTC[-/T]TTTTTTTTTAAGACT | 55130 |
| rs199871429 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27890785 | TAAAAAAAAAAAAAA[-/A]CTTGTATTATCATTC | 55130 |
| rs199871988 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27968377 | ACTGTGAGATTGTAA[C/T]AAAAGCGCTAATATC | 55130 |
| rs199875677 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27977771 | ATAGGATATGTGAAT[A/G]GCCAATAAGCACATG | 55130 |
| rs199879626 | snp | C/T | | | missense, intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27971210 | TCCAGTGACCTTTTG[C/T]CTGAACCAGAAATGT | 55130 |
| rs199881398 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27988011 | AACAAAAAAACTATG[-/A]AAAAAAAAAGCAAAC | 55130 |
| rs199893699 | in-del | -/TA | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27859227 | GTCCAATATGTTTTT[-/TA]TATAGTTTACTTTTA | 55130 |
| rs199917821 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27903548 | TTGTATATTTAGAAA[A/C]CCCATCGTCTCAGCC | 55130 |
| rs199939551 | in-del | -/C | 0.0505692 | 0.150756 | intron-variant, frameshift-variant | ARMC4 | GRCh38.p7 | 10:27853329 | CCAAGATCGTTGTCA[-/C]TGCACTCTAGCCTGG | 55130 |
| rs199983222 | snp | C/G | 0.498034 | 0.0312882 | intron-variant | ARMC4 | GRCh38.p7 | 10:27847539 | CCCTCTCTCACCCCT[C/G]CTATTCAACATAGTG | 55130 |
| rs199988449 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27973917 | TGTGTACGTATTCCC[-/T]TTTTTTCTGCAACTT | 55130 |
| rs200046648 | in-del | -/TTTTTCT | 0.0166325 | 0.0896639 | intron-variant | ARMC4 | GRCh38.p7 | 10:27869535 | TTTTTTTCTTTTTTC[-/TTTTTCT]TTTTTTTTTTTGAGA | 55130 |
| rs200069530 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27969790 | TCACCTACAGGCTGC[A/G]ACTTGTAAACTATTT | 55130 |
| rs200085145 | snp | C/T | 0.000927669 | 0.0215168 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944180 | AGCTGTGTGCAGTGG[C/T]GGCTGGCACTAGATG | 55130 |
| rs200127444 | snp | C/T | 0.000247188 | 0.0111145 | missense | ARMC4 | GRCh38.p7 | 10:27940663 | ATGCCCCCAGCTTTG[C/T]GGATGGCTTCTTTAT | 55130 |
| rs200159785 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27964975 | AAGAAGGGTACTTCT[A/G]GTGATAATTCCAGGA | 55130 |
| rs200208473 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27961322 | GTCACAGTGTCAGCT[C/G]TTTACCATGCCCACT | 55130 |
| rs200216460 | in-del | -/G | 0.0295035 | 0.117819 | intron-variant | ARMC4 | GRCh38.p7 | 10:27958512 | ACTGGCAACTGGTTT[-/G]TTTTTATTTTAAGAC | 55130 |
| rs200232814 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27891318 | TCTCAAATTCCTGAC[A/G]GGCTTCTCAGTTTGG | 55130 |
| rs200235112 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27921312 | ACGAAAAAAAAAAAG[A/G]AAAAAAAAAGAACAT | 55130 |
| rs200236014 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27965317 | GGTTACACAGAGCCT[A/G]GGGAAAAGAAGATCT | 55130 |
| rs200249154 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27922153 | AGTGAAACTCTGCCT[A/C]AAAAAAAAAAAAAAA | 55130 |
| rs200261733 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27893557 | AATCCAAACAAAGAC[G/T]TTATTTCAAAGTGAT | 55130 |
| rs200273841 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27887674 | ATTTGCAGCAGAAGG[-/A]AAAGTGGAAAATTCA | 55130 |
| rs200299490 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27909843 | AAAAAAAAAAAAAAA[C/T]ACTCAGAACACTACG | 55130 |
| rs200299616 | snp | A/C/T | 4.96039e-05 | 0.00497995 | missense, stop-gained | ARMC4 | GRCh38.p7 | 10:27935245 | CAATGGCTTTGTATT[A/C/T]CCGAAACCTAAGTTC | 55130 |
| rs200303688 | snp | A/T | 0.000101348 | 0.00711784 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940844 | GTTCATGGAAATCTT[A/T]AAAAGAACATTTAAG | 55130 |
| rs200311436 | snp | A/C/T | 0.000265571 | 0.0115203 | intron-variant | ARMC4 | GRCh38.p7 | 10:27935265 | AACCTAAGTTCATCA[A/C/T]AAGAAAGAGGAGAAT | 55130 |
| rs200311460 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27943763 | TCGCGCCACTGCACT[C/G]CAGCCTGAGCCACAG | 55130 |
| rs200331622 | in-del | -/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27941339 | AAAAAAAAAAAAAAA[-/G]CTGGATGTGGTGGTG | 55130 |
| rs200363248 | snp | C/T | 0.000478844 | 0.0154659 | missense | ARMC4 | GRCh38.p7 | 10:27907701 | AGAGTGCCCATGCTG[C/T]GCTGGCCTTCACGTC | 55130 |
| rs200379996 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27898336 | AATTTCCAAAAAAAA[-/T]CAGTTTTAAGCCTAT | 55130 |
| rs200460159 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27937942 | ATTCATATATAGAGG[-/T]TTTTTTGTTTTTTGT | 55130 |
| rs200461898 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27846155 | GTACTTATTCCAAAA[C/T]TGACCACATAGTTGG | 55130 |
| rs200464359 | in-del | -/A | 0.0322114 | 0.122752 | intron-variant | ARMC4 | GRCh38.p7 | 10:27887836 | CAGACTTTAAATTAG[-/A]TTTTAAAAAAGTGGG | 55130 |
| rs200470315 | in-del | -/T | 0.0752113 | 0.178743 | intron-variant | ARMC4 | GRCh38.p7 | 10:27849352 | GTGGGAATTGAAAAA[-/T]GAGAACACTTGGACA | 55130 |
| rs200483471 | in-del | -/TATATA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27827380 | TACACACACACACAC[-/TATATA]TATATATATATATAT | 55130 |
| rs200508883 | snp | A/C | 3.30338e-05 | 0.00406397 | synonymous-codon, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983909 | ATCGTGAGGTTTCAC[A/C]AGCACATAACAAATT | 55130 |
| rs200509517 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27962919 | TATTCCTCATCTCAC[A/G]GGACAGAAGCAAACT | 55130 |
| rs200513953 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27905435 | TCATGAAAATGGCCA[C/T]ACTGCCCAAAGTAAT | 55130 |
| rs200519154 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27833388 | AACTGAAAAAAAAAA[-/T]CAAGGAGGAAAATTA | 55130 |
| rs200542560 | in-del | -/T | | | downstream-variant-500B, intron-variant | ARMC4 | GRCh38.p7 | 10:27811674 | ATAAAATGCTATTTG[-/T]TTTTGTAGCCACTTT | 55130 |
| rs200574441 | snp | A/G | 0.00300417 | 0.0386401 | missense | ARMC4 | GRCh38.p7 | 10:27995057 | ATTTCTTTCAATATC[A/G]CTTCATTTAGAGGGG | 55130 |
| rs200634787 | in-del | -/TTC | 0.02016 | 0.0983543 | intron-variant | ARMC4 | GRCh38.p7 | 10:27877526 | TGAGATTTCTTTCTT[-/TTC]TTTTTTCCTTTTTAG | 55130 |
| rs200660061 | in-del | -/TTTGG | 0.0170251 | 0.090679 | intron-variant | ARMC4 | GRCh38.p7 | 10:27876755 | CGGGGTCAGCTACAC[-/TTTGG]TTTGGTTTGTCCAAG | 55130 |
| rs200670361 | in-del | -/GG | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27924014 | AAAGAAAGAAAGAAA[-/GG]GAAAGAAAGAAGGAA | 55130 |
| rs200672255 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27891379 | TACTAGAGTTTTTTG[-/T]TTTTTTTTTTTCCTT | 55130 |
| rs200681074 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27969721 | GCAGGAGAAGGTCCC[C/T]GTGTGATCAACCAGG | 55130 |
| rs200697842 | snp | C/T | 0.498059 | 0.0310896 | intron-variant | ARMC4 | GRCh38.p7 | 10:27847534 | GGATGCCCTCTCTCA[C/T]CCCTGCTATTCAACA | 55130 |
| rs200699327 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27892309 | AAAAATATGCAGATT[-/A]ATTTTTTATGACTAG | 55130 |
| rs200702553 | snp | A/G | 0.000541646 | 0.0164478 | intron-variant, utr-variant-3-prime | ARMC4 | GRCh38.p7 | 10:27939857 | TACCTTAAACTATGT[A/G]AGAAAGAACGCCAAC | 55130 |
| rs200748552 | in-del | -/C | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27959384 | GCCAGTTCTTTTTTT[-/C]TTTCCCCCAGATGAC | 55130 |
| rs200751768 | in-del | -/AAG | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27931121 | CTCTGCTCTCTTAAA[-/AAG]AAAAAAGAAAGAAAG | 55130 |
| rs200760656 | snp | C/T | 0.000256058 | 0.0113121 | intron-variant | ARMC4 | GRCh38.p7 | 10:27961729 | TCCTAAGAACAATAA[C/T]AACACACATACACAT | 55130 |
| rs200765192 | in-del | -/AAAT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27970102 | AGATTCTGTCTCAAA[-/AAAT]AAATAAATAAATAAA | 55130 |
| rs200778612 | in-del | -/TA | | | utr-variant-3-prime, intron-variant | ARMC4 | GRCh38.p7 | 10:27812189 | AGGCCATATCCTTTT[-/TA]TTAAAATCGCCACAA | 55130 |
| rs200805282 | in-del | -/G | 0.0275645 | 0.114116 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999676 | TGGGAATATTGAGGT[-/G]GGGGGGGATGGGGAA | 55130 |
| rs200806071 | snp | A/G | 0.286303 | 0.24735 | intron-variant | ARMC4 | GRCh38.p7 | 10:27993976 | TATATATATATATAT[A/G]TGTGTGTGTGTGTGT | 55130 |
| rs200857580 | in-del | -/GAAAGTGC | 0.0248432 | 0.108648 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:28000279 | TTTTCTTCTCTTTTT[-/GAAAGTGC]GAAAGTTGTTAGGAA | 55130 |
| rs200875268 | snp | A/C | 6.59587e-05 | 0.00574239 | missense, intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27971203 | GTTCTTCTCCAGTGA[A/C]CTTTTGTCTGAACCA | 55130 |
| rs200893584 | snp | A/C | 1.64993e-05 | 0.00287218 | missense | ARMC4 | GRCh38.p7 | 10:27987440 | TGGCAATAAGTAACA[A/C]GCGTGACAGCTGCCC | 55130 |
| rs200920382 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27970350 | GTTCTGTTAGACATT[A/C]TCTCTATGACAGTTT | 55130 |
| rs200925571 | in-del | -/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27920860 | CCCAATGTAAAAACT[-/G]GAAAAAAAAAAACTA | 55130 |
| rs200928629 | snp | A/G | 1.65693e-05 | 0.00287826 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940549 | GGCAAGGGAAGCAGA[A/G]CTGGCATGAGTACCT | 55130 |
| rs200934236 | snp | A/G | 1.64808e-05 | 0.00287057 | synonymous-codon, missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27812539 | TGCCTTCTCTGTAGC[A/G]AGAGCCAGCCTGCGG | 55130 |
| rs200985278 | snp | A/T | 3.39155e-05 | 0.00411784 | missense | ARMC4 | GRCh38.p7 | 10:27862621 | ACCATTTCCCCAGCA[A/T]CCTAGACAAAAATAA | 55130 |
| rs201007763 | in-del | -/A | 0.0322114 | 0.122752 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872708 | CCAGGGATGAAGCCC[-/A]CTTGATCATAGTGGA | 55130 |
| rs201013122 | in-del | -/A | 0.031825 | 0.122064 | intron-variant | ARMC4 | GRCh38.p7 | 10:27829109 | AGAGAATTAAAAAGG[-/A]AAAAAAAAAGAAACA | 55130 |
| rs201056632 | snp | C/T | 3.30475e-05 | 0.00406481 | missense, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983896 | ACAGAGTCTCACCAT[C/T]GTGAGGTTTCACCAG | 55130 |
| rs201080776 | in-del | -/AAAAAAAA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27909818 | GTGAGTCTTCATTTG[-/AAAAAAAA]AAAAAAAAAAAAAAA | 55130 |
| rs201117549 | snp | A/G | 1.65957e-05 | 0.00288055 | intron-variant | ARMC4 | GRCh38.p7 | 10:27935264 | AAACCTAAGTTCATC[A/G]TAAGAAAGAGGAGAA | 55130 |
| rs201152921 | in-del | -/AA | 0.330249 | 0.23677 | intron-variant | ARMC4 | GRCh38.p7 | 10:27921736 | AAAAATCCCCAGTCC[-/AA]AAAAAAAAAAATCAA | 55130 |
| rs201168271 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27973578 | ATTTATAAGTGGAAC[A/C/G]GGGGGTAATATGTTT | 55130 |
| rs201180724 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27979442 | AATACACACACACAC[A/C]CATACACACACACAC | 55130 |
| rs201191370 | in-del | -/ATA | 0.0410537 | 0.137264 | intron-variant | ARMC4 | GRCh38.p7 | 10:27901971 | CTAATAGACATCTAC[-/ATA]ACTCTCCACCCCAGA | 55130 |
| rs201203284 | snp | C/T | 0.00218593 | 0.0329877 | intron-variant | ARMC4 | GRCh38.p7 | 10:27907784 | TCAATTATCCTATCG[C/T]GGAACCCAAAATCAT | 55130 |
| rs201213030 | snp | C/T | 0.000131811 | 0.00811715 | stop-gained, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27936759 | CTGATGGAACATTTC[C/T]ATATAGCCCCTGTGA | 55130 |
| rs201245684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27833643 | TGGGACAAAAAATTG[A/G]GGAAAATAGTTCATT | 55130 |
| rs201270278 | in-del | -/TATA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27827380 | TACACACACACACAC[-/TATA]TATATATATATATAT | 55130 |
| rs201275479 | snp | C/T | 1.64996e-05 | 0.0028722 | missense | ARMC4 | GRCh38.p7 | 10:27987431 | TCCCAGTTTTGGCAA[C/T]AAGTAACAAGCGTGA | 55130 |
| rs201295650 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27823894 | GCCTGTAATCCCAGC[A/G]CTTTGGGAGGCCGAG | 55130 |
| rs201296121 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27880261 | AGAATCTTTTAGATA[C/T]AAATTTCACCTTGTG | 55130 |
| rs201305183 | in-del | -/A | 0.0225045 | 0.103662 | intron-variant | ARMC4 | GRCh38.p7 | 10:27918053 | AGGAATCCTTTTCAT[-/A]AAAAAAAACTCCAAC | 55130 |
| rs201330310 | snp | C/T | 0.000182199 | 0.00954287 | intron-variant | ARMC4 | GRCh38.p7 | 10:27934963 | TGACCTCCCAAGTGT[C/T]CTCCCTAACACTTAT | 55130 |
| rs201350893 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27918497 | TAAAATTCAAAAATC[C/T]ATTTTTATTAAAATA | 55130 |
| rs201388785 | snp | C/T | | | utr-variant-3-prime, intron-variant | ARMC4 | GRCh38.p7 | 10:27812186 | GGAAGGCCATATCCT[C/T]TTTATTAAAATCGCC | 55130 |
| rs201391225 | in-del | -/ACTA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27958701 | TTATTGCCAACAGTT[-/ACTA]ACTACTTTGTGCTAA | 55130 |
| rs201408649 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27859999 | TGTGTTAAGTAAACA[C/T]TATAGCCAATAGAAT | 55130 |
| rs201438550 | in-del | -/ATTATTATTATTATTATT | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27960314 | TTATTTATTTATTTC[-/ATTATTATTATTATTATT]ATTATTATTATTATT | 55130 |
| rs201441923 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27846180 | AGTTGGAAGTAAAGC[A/T]CTCCTCAGCAAATGT | 55130 |
| rs201446595 | snp | C/T | 0.000991735 | 0.022246 | utr-variant-3-prime, intron-variant | ARMC4 | GRCh38.p7 | 10:27812476 | ACATGTCCTGTGTCA[C/T]GTAGAATTTGATAGC | 55130 |
| rs201456745 | snp | A/G | 3.32419e-05 | 0.00407675 | intron-variant | ARMC4 | GRCh38.p7 | 10:27936887 | TTCAGCACACTGCAC[A/G]AAAAGTCAGACAGAG | 55130 |
| rs201480933 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27890769 | TCTGGTATATATATA[-/T]TTAAAAAAAAAAAAA | 55130 |
| rs201484123 | in-del | -/TT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27969554 | TTTTCACATTGACTC[-/TT]TCAAACAGAGCCACA | 55130 |
| rs201498403 | snp | C/G | 0.000412572 | 0.0143567 | missense | ARMC4 | GRCh38.p7 | 10:27935221 | CTGTTAGAAGTCCCA[C/G]CAAGGTTTCAATGGC | 55130 |
| rs201506550 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27893022 | GGCATGGGGCTGCAT[A/G]CTTGTCCATTCCTGT | 55130 |
| rs201532806 | snp | A/C | 0.498034 | 0.0312882 | intron-variant | ARMC4 | GRCh38.p7 | 10:27847536 | ATGCCCTCTCTCACC[A/C]CTGCTATTCAACATA | 55130 |
| rs201535511 | snp | A/G | 0.172674 | 0.237741 | intron-variant | ARMC4 | GRCh38.p7 | 10:27976215 | ACCATTTCTATTCAA[A/G]TTTTTACTGGTGATT | 55130 |
| rs201550932 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27938597 | TGTATCTGTCTCTTC[-/T]TTTTTTCTTTTTTTT | 55130 |
| rs201555724 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27926026 | AAAAAAAAAAAAAAG[A/T]AACACTTTCTCTAAT | 55130 |
| rs201573380 | in-del | -/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27923034 | AGATAACCACTAGAA[-/C]CAAAAATGCAAACCT | 55130 |
| rs201617006 | snp | C/T | | | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27995047 | AAACACAATAATTTC[C/T]TTCAATATCGCTTCA | 55130 |
| rs201693991 | snp | A/G | 1.66813e-05 | 0.00288797 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940531 | AGAAAGTCAAGTTGA[A/G]AAGGCAAGGGAAGCA | 55130 |
| rs201701781 | in-del | -/CAC | 0.0539704 | 0.155153 | intron-variant, cds-indel | ARMC4 | GRCh38.p7 | 10:27853332 | AGATCGTTGTCACTG[-/CAC]TCTAGCCTGGCGACA | 55130 |
| rs201708409 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27819834 | AGACCTTATCTCTTT[A/T]AAAAAAAAAAAAAGG | 55130 |
| rs201715058 | in-del | -/A | 0.221737 | 0.248397 | intron-variant | ARMC4 | GRCh38.p7 | 10:27951627 | ACTTAAAAAAAAAAA[-/A]GCTATAAAACTAACA | 55130 |
| rs201733942 | in-del | -/T | | | intron-variant, frameshift-variant | ARMC4 | GRCh38.p7 | 10:27853326 | GAGCCAAGATCGTTG[-/T]CACTGCACTCTAGCC | 55130 |
| rs201738036 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27862793 | TGTATATGTATAAAG[A/T]GTGTGTGTGTACATA | 55130 |
| rs201738659 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27870540 | CCCCAGTGTGTGATG[G/T]TCCCCTTCCTGTGTC | 55130 |
| rs201801775 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27940261 | TATAAATGTCAGTAT[A/G]TGTGATATATATATA | 55130 |
| rs201805589 | in-del | -/AT | 0.0295035 | 0.117819 | intron-variant | ARMC4 | GRCh38.p7 | 10:27868380 | AAGACACATGCACAC[-/AT]ATGTTTATCGCAGCA | 55130 |
| rs201834298 | snp | A/G/T | 0.000230722 | 0.0107382 | missense | ARMC4 | GRCh38.p7 | 10:27860749 | TAACGCACTAGTGGA[A/G/T]CCACTGCTTTGTGCT | 55130 |
| rs201844076 | snp | A/C | 0.0174333 | 0.0917209 | intron-variant | ARMC4 | GRCh38.p7 | 10:27969028 | CCTTTGCTTTAAAAA[A/C]ATATACAAATATATT | 55130 |
| rs201906114 | in-del | -/A | 0.184521 | 0.241273 | intron-variant | ARMC4 | GRCh38.p7 | 10:27920861 | ACTGAAAAAAAAAAA[-/A]CTATGTAAATGCAAC | 55130 |
| rs201908864 | snp | A/C/G | 8.24281e-05 | 0.00641938 | missense | ARMC4 | GRCh38.p7 | 10:27860647 | GCACCATTCTCATGC[A/C/G]TGGTGATGCAGTTAT | 55130 |
| rs201959559 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27964273 | TTAGTGAAGTGGCTG[G/T]GCTAAAACACATAGT | 55130 |
| rs201983611 | in-del | -/TA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27870009 | ATATATATATATATA[-/TA]GTTGGAAGTATAAAA | 55130 |
| rs201990903 | snp | C/T | 0.00199792 | 0.0315431 | missense, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27936778 | TAGCCCCTGTGACAG[C/T]AGCTAACCGCTCTTT | 55130 |
| rs201992795 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27969738 | TGTGATCAACCAGGA[A/G]TCAGTTCTTAACCCA | 55130 |
| rs202026696 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27824162 | AAAAAAAAAAAAAAA[A/T]AAAAATAGTTCAATA | 55130 |
| rs202038219 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27971007 | AAATAAATAAATAAA[C/T]AAACAAACAAACAAA | 55130 |
| rs202041744 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27986790 | TTAGATGATTAGATG[-/A]ATAGTGTGAACATCA | 55130 |
| rs202042471 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27974704 | GTTTTTTTTTTTTTT[G/T]CTTAGGATTGCCTTG | 55130 |
| rs202073100 | in-del | -/T | 0.0126979 | 0.078662 | intron-variant | ARMC4 | GRCh38.p7 | 10:27894742 | ATTAAAAAAAAAAAA[-/T]AATTGTTGTAGAGGA | 55130 |
| rs202097819 | snp | C/G | 0.227664 | 0.249 | intron-variant | ARMC4 | GRCh38.p7 | 10:27979473 | ACACACACACACACA[C/G]AGTTAAATGAATTCA | 55130 |
| rs202109225 | snp | A/T | | | downstream-variant-500B, intron-variant | ARMC4 | GRCh38.p7 | 10:27811670 | ACCCGATAAAATGCT[A/T]TTTGTTTTGTAGCCA | 55130 |
| rs202118841 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27820145 | TAGCTTCTGTCAGCA[A/C]CTGCTCCAGGCCCTG | 55130 |
| rs202130719 | snp | C/T | 0.00010147 | 0.00712211 | intron-variant | ARMC4 | GRCh38.p7 | 10:27987342 | ACTTTCCCAGCAAGA[C/T]TGTTTCTAAAAGTTC | 55130 |
| rs202135777 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27822789 | TGTCCTCCTCAAGGT[A/G]ATAGGTGTGTGTGTG | 55130 |
| rs202145088 | snp | C/T | 0.000256904 | 0.0113308 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944197 | GCTGGCACTAGATGA[C/T]GATGACAACATCACG | 55130 |
| rs202158969 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27963648 | ACCAATAATAGACTA[-/A]TTTATGGTCTTAATT | 55130 |
| rs202172824 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27907903 | ATTTTTTTTTTTTTT[A/C]CAAAACTTCATCAAC | 55130 |
| rs202214530 | in-del | -/T | 0.0107246 | 0.0724382 | intron-variant | ARMC4 | GRCh38.p7 | 10:27937066 | AGCATGTCTCTCTCC[-/T]TATGTGGCTTTGGGA | 55130 |
| rs267602460 | snp | A/G | | | missense | ARMC4 | GRCh38.p7 | 10:27860725 | ACGTTGGTGTCATTT[A/G]ATTTCAGATAACGCA | 55130 |
| rs267602461 | snp | A/G | | | stop-gained | ARMC4 | GRCh38.p7 | 10:27935074 | TCACAAGAAGAGCTT[A/G]GTTTATTCCAACAAG | 55130 |
| rs267602462 | snp | C/T | | | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27939975 | AAGGTTTTCAATGAT[C/T]CTTTCTGCTTTGATT | 55130 |
| rs267602463 | snp | A/G | | | missense | ARMC4 | GRCh38.p7 | 10:27995069 | ATCGCTTCATTTAGA[A/G]GGGTGATTTCGAGGA | 55130 |
| rs367558112 | in-del | -/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27816840 | TGCAACCTCCGTCCC[-/C]TGGGGTTCAAGTGAT | 55130 |
| rs367592924 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARMC4 | GRCh38.p7 | 10:27816839 | CTGCAACCTCCGTCC[C/T]CTGGGGTTCAAGTGA | 55130 |
| rs367630312 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27821010 | GTTTCAAATTCCTGA[C/T]CTTAAGTGATCTGCC | 55130 |
| rs367651620 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27826368 | ATCTCTAATTTCCAT[C/T]GGCTCTCCGTGTTGC | 55130 |
| rs367653850 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27955731 | TGTGTGTGTGTGTGT[G/T]TGTGTGTGTGTTTAA | 55130 |
| rs367662719 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27826985 | CCTATTTCCTCACTT[C/T]TTATTCAAGGCCATT | 55130 |
| rs367713384 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27829437 | TCCTTCCATTTACCC[C/T]GTTGATATCAAGTGT | 55130 |
| rs367781502 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27906312 | AAAACCACAATGAGA[C/T]ACCATCTCACACCAG | 55130 |
| rs367805042 | snp | C/T | 1.65089e-05 | 0.00287301 | intron-variant | ARMC4 | GRCh38.p7 | 10:27860622 | AAAGTCATTCAACTG[C/T]ACCTTTACTGCACCA | 55130 |
| rs367829233 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27858744 | AGAAGAAATAATTGC[A/G]AGTTGCATATACACC | 55130 |
| rs367837712 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27877387 | AGGAGCCAAAGTCCC[C/T]GTGAGATCATGGGCA | 55130 |
| rs367852553 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27871509 | ACATTTAAGTCTTTA[A/T]TCCATCTTGAATTAA | 55130 |
| rs367876719 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997586 | AGAAATGTAACATTT[A/G]AATCTATTCAAATTG | 55130 |
| rs367878016 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27847578 | TCTGGCCAGGGCAAT[C/T]AGGCAGGAGAAAGAA | 55130 |
| rs367885333 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27927745 | CTCTTCTAGTTCCCC[A/G]CTCAACTCTCTGGCT | 55130 |
| rs367906264 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27845542 | AACCAGCTAACATCA[C/T]AATGACAGGATCAAA | 55130 |
| rs367921392 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27986534 | ATAAGGAGTAATAGG[C/T]AAGGCATAAAAAGAG | 55130 |
| rs367930896 | in-del | -/AA/AAA/AAAA | 0.482683 | 0.0914256 | intron-variant | ARMC4 | GRCh38.p7 | 10:27895041 | CTAGTCATCGGTACG[-/AA/AAA/AAAA]AAAAAAAAAAAAAAC | 55130 |
| rs367950514 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27885527 | AAAAAAAAAAAAAAA[A/T]AAAAAAATATATATA | 55130 |
| rs367977565 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27831174 | CCTCTGCAGATAATG[A/C]TACCTCGGCCTGCAA | 55130 |
| rs367978453 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27884505 | TTCCTTCAGCCGGAA[A/G]GACCAAAGTGGAAGT | 55130 |
| rs367991055 | snp | A/G | 0.000132641 | 0.00814267 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940547 | AAGGCAAGGGAAGCA[A/G]AACTGGCATGAGTAC | 55130 |
| rs368031714 | snp | G/T | 6.60186e-05 | 0.00574499 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944798 | AGACTCCGCATCCAA[G/T]GTGACAGAGCCACTC | 55130 |
| rs368055260 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | ARMC4 | GRCh38.p7 | 10:27907632 | TAGTATTAGAGATTC[C/T]AGAAGAGACTGACTT | 55130 |
| rs368062829 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | ARMC4 | GRCh38.p7 | 10:27930457 | CATTCAAGGCTGCAG[G/T]GAACAATGATGGCAC | 55130 |
| rs368075584 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | ARMC4 | GRCh38.p7 | 10:27977070 | TTGATCCATAACTCA[C/T]ATACACAAACCAAAT | 55130 |
| rs368075866 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27923202 | AACTCATTAAAACAA[A/C]AACTATGTTTAATTG | 55130 |
| rs368079133 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27855968 | ATGCCTTTAATAGGT[A/G]CTCATCAGTCTTCTA | 55130 |
| rs368087120 | snp | C/T | 0.00166392 | 0.0287957 | utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27995149 | CACACCCATGGGATC[C/T]ACCGTGCTCAGACCT | 55130 |
| rs368091306 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27946947 | CCTCAACAACTGTCC[C/T]GTGAAGATGTCACTG | 55130 |
| rs368096770 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27879880 | CTCATCCTTTCTGCT[G/T]TGTACCTTTAGCCAA | 55130 |
| rs368104955 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27887794 | CAATGAAAGCAAGAG[C/T]TGGTTACTCAAAAAG | 55130 |
| rs368161858 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27950638 | GTCGTGCGGGCTGGA[A/G]TGCAACGGTGTGATC | 55130 |
| rs368191329 | in-del | -/G | | | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999716 | ATCTTGGGGTGGGGG[-/G]ACACGGTGTTTAAGG | 55130 |
| rs368237525 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27975251 | TAAATTAAACGTATT[C/G]TAACATTTTTTAAAA | 55130 |
| rs368258725 | snp | A/T | | | intron-variant, splice-acceptor-variant | ARMC4 | GRCh38.p7 | 10:27853365 | TGGCGAGACTCTGTC[A/T]ATAAATAAATAAATA | 55130 |
| rs368272847 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27912370 | GCAAAATAACAGCTC[G/T]AGAAAGATGAATACA | 55130 |
| rs368319585 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27832274 | TTGCCTGGACACAAT[A/G]TCTCTGGGTCTCTCT | 55130 |
| rs368329710 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27973635 | TCTTTTTTATGGCTG[G/T]GTAGTATTCCATGGC | 55130 |
| rs368340868 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27860262 | TTCAAGACCAGCCAG[A/G]GCAGCATGGCAAGAC | 55130 |
| rs368379363 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27823371 | AATTCTCTGGAAAAA[A/T]ATATTCCCATAGATT | 55130 |
| rs368422075 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ARMC4 | GRCh38.p7 | 10:27965974 | TTCTCTCCCTCCTCT[A/G]CTCTCTTCAACTCCC | 55130 |
| rs368454299 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27924031 | AAGAAAGAAGGAAAG[A/G]GAAAGAAAGAAGGAA | 55130 |
| rs368480023 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27935719 | AAAAAAAAAAAGTCA[C/G]TCTCAGGTATCTTCT | 55130 |
| rs368501109 | snp | A/T | 0.000153988 | 0.00877328 | missense | ARMC4 | GRCh38.p7 | 10:27994993 | TTCCACAAAAACAAA[A/T]TTTGCCTCTTGAGGA | 55130 |
| rs368502664 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27911873 | ACCACACTCCCAGCA[A/G]GCTACCACACCAGTG | 55130 |
| rs368504148 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27903950 | CTTCCTCCCCTCTGG[G/T]GTTCCCTTTAGACCT | 55130 |
| rs368517194 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27932473 | TTAATAGTCACAGAA[A/T]GATTAAAAGATGATT | 55130 |
| rs368532421 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27924507 | AGATAAAACCAGAAA[C/T]TTATGTGGTAGAAAA | 55130 |
| rs368534066 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27908971 | AAGTAGGTTTTCAAA[C/T]CTAAAACTTTCATAC | 55130 |
| rs368538204 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27935257 | ATTCCCGAAACCTAA[A/G]TTCATCATAAGAAAG | 55130 |
| rs368560892 | snp | C/T | 1.65608e-05 | 0.00287752 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27940797 | ATGTGCACAGTCTAG[C/T]AGAGCAACCTATAAT | 55130 |
| rs368564627 | snp | C/G | 1.66272e-05 | 0.00288328 | intron-variant | ARMC4 | GRCh38.p7 | 10:27860595 | ACATTTACCAAACTT[C/G]GACTAAACCACAAAG | 55130 |
| rs368584891 | snp | A/G | 3.39029e-05 | 0.00411707 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983823 | ACTGGCTTTAGTTAC[A/G]TTTTTAAAAATTTAC | 55130 |
| rs368609877 | snp | C/T | | | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27857895 | TGTACAACTGGAAAA[C/T]AACAAGCATTTGACG | 55130 |
| rs368633322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27960082 | ATTTATAAAGTATCA[C/T]GCTTAAAATGAAATT | 55130 |
| rs368642943 | snp | A/G/T | 0.000171855 | 0.00926823 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940026 | GGAATAAAAACCTAC[A/G/T]TATTTATGTGTTCAA | 55130 |
| rs368644776 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27888209 | GATCAAATGGTAGTT[C/G]TATTTTTAGTTCTTT | 55130 |
| rs368668929 | snp | A/G | 1.83333e-05 | 0.00302759 | intron-variant, utr-variant-3-prime | ARMC4 | GRCh38.p7 | 10:27939867 | TATGTGAGAAAGAAC[A/G]CCAACAACCGCTGGG | 55130 |
| rs368698655 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27937573 | TAAATATTTACTGCA[A/C]AGATGGTCTCAACTG | 55130 |
| rs368738464 | snp | A/T | 0.0197687 | 0.0974348 | intron-variant | ARMC4 | GRCh38.p7 | 10:27889661 | TTCTGATCTCACAGT[A/T]TCACACATGGACACT | 55130 |
| rs368745698 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27994592 | TATGTGTATATATAT[C/G]TCCACATATGGGTGG | 55130 |
| rs368837272 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27906034 | GATTGAATTAAACTA[A/G]AAAGCTCTGCACAGC | 55130 |
| rs368853967 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27940997 | AAAAACCTTCCTCCA[C/G]ATTTGGGAGCTTATA | 55130 |
| rs368873346 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27926351 | CATACAGAATTCAAC[A/G]GAGCTCATTAAAAAC | 55130 |
| rs368894500 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27960978 | CAAATACTTAAATAC[A/G]TTACATGGGCCAATT | 55130 |
| rs368953904 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27944563 | CCCAGAGGTTACACA[C/T]ATCTGGCATATTCTC | 55130 |
| rs369004195 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27998998 | CAGTCCGTTACCCTG[C/G]TCTCGGGACCTCCGC | 55130 |
| rs369022423 | snp | C/T | 8.24151e-05 | 0.00641878 | missense | ARMC4 | GRCh38.p7 | 10:27860666 | TGATGCAGTTATCGG[C/T]GTCTTCTGAGAGTTG | 55130 |
| rs369032642 | snp | A/G | 3.29533e-05 | 0.00405901 | synonymous-codon, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27936734 | CTCTTACTTGGTAAC[A/G]TTCTCTTTGCTGATG | 55130 |
| rs369043170 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27890503 | GTTTAGAATAGGCAA[C/T]GCTTTTCGTTGTAAG | 55130 |
| rs369080078 | in-del | -/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27942448 | TCAGTTAGTCTATAG[-/G]AAAACTGGTTTTGTT | 55130 |
| rs369106062 | snp | A/G | | | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999176 | TTCTCAAACACTTTT[A/G]TGCAACTCCCGAGTG | 55130 |
| rs369112803 | in-del | -/G | | | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999676 | TTGAGGTGGGGGGGG[-/G]ATGGGGAAGAATGCA | 55130 |
| rs369121543 | snp | A/G | | | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27996121 | CGTTCTGACTTCATA[A/G]TGAACATTTAATGCT | 55130 |
| rs369149022 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27989608 | TGAAACTCCTGGTGA[A/G]AAGCCAAAGGGCACA | 55130 |
| rs369231462 | in-del | -/ATAT | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27961014 | GTAAAATATTCTCAT[-/ATAT]GCTATCTGACGTGAG | 55130 |
| rs369264618 | snp | A/G | 0.00013222 | 0.00812974 | missense | ARMC4 | GRCh38.p7 | 10:27907767 | GAACTCCATCTAAGC[A/G]ATCAATTATCCTATC | 55130 |
| rs369277630 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27831020 | AGATGTGATGTTAAA[G/T]GCACCATGAGAAAAA | 55130 |
| rs369282975 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27859873 | AACATGTCTTTGAAT[A/C/T]TATCTATTGTTGTTA | 55130 |
| rs369287573 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27823849 | TCTCTATGTTCATAA[A/G]AATAGTTCAGGCCGG | 55130 |
| rs369294270 | snp | C/T | 0.000153988 | 0.00877328 | missense, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27961678 | CACTTTCTGAGGAGC[C/T]ATCGCTAACAGTTTC | 55130 |
| rs369296315 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27885533 | AAAAAAAAAAAAAAA[A/T]ATATATATATATATA | 55130 |
| rs369318955 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27870782 | GGGTTGGTTCCAAGT[A/C]TTTGCTATTGTGAAT | 55130 |
| rs369323142 | in-del | -/AAAG | 0.010348 | 0.0711822 | intron-variant | ARMC4 | GRCh38.p7 | 10:27931125 | TGCTCTCTTAAAAAA[-/AAAG]AAAGAAAGAAAGAAA | 55130 |
| rs369323249 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27847850 | AATAAAATACCTAGG[A/C/G]ATCCAACTTACAAGG | 55130 |
| rs369370915 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27937319 | CAAATATATTTTCTT[C/T]TTTTCTTTCTTTCTT | 55130 |
| rs369406467 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27963103 | ACCTCCGCCTGCCGG[A/G]TTCATGTGATTCTCC | 55130 |
| rs369450929 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27881238 | AAAATAATCAATCTA[A/G]TGAATAACCACTTGA | 55130 |
| rs369473624 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27900403 | CAAAAACCAGAACAT[C/T]TCTTCTCCAAAGGAT | 55130 |
| rs369474179 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27885812 | TATATAAAATATATA[A/T]TATATATAATATATA | 55130 |
| rs369481896 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27998086 | AACCCATTCGGTAAT[C/T]ACATCGTTAACACTT | 55130 |
| rs369489608 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27916886 | TAACCCCTGTGTTGT[G/T]CAAGGGACAGCTCTA | 55130 |
| rs369493712 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27989840 | AGTGACAGAGTGAGA[A/C]CCCCTCTCAAAAAAT | 55130 |
| rs369513329 | snp | A/G | | | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999058 | CCGTATGCCCGCGCC[A/G]GAGACGCTCTGCGCC | 55130 |
| rs369574339 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27947339 | GTGTGGAGGCATGCA[A/C]CTGTAATCTCAGCTA | 55130 |
| rs369634645 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27835410 | ACAATTCTACTCCTA[C/T]AACAACAACAACCGC | 55130 |
| rs369654608 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27835484 | TCTCTCTCTCTGTAC[A/G]GTTGATGTCTGAAAA | 55130 |
| rs369660209 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27939193 | GTAGGAGATAAATGC[C/T]CCAAGATTATTTGAA | 55130 |
| rs369667087 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27856735 | GGGTACAAAGGCCGA[G/T]GTGGGTGGATCACCT | 55130 |
| rs369669370 | snp | A/G | 8.2513e-05 | 0.00642259 | stop-gained, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983938 | TTTCCCCACGAATTT[A/G]TCTCCACGGTGGGGC | 55130 |
| rs369678646 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27825707 | GGTACAGGAACAAGA[A/C/T]AATCCATAGCCTGGA | 55130 |
| rs369679170 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27828226 | GAAGAGCTAGGAGCA[A/G]CTGGGGCAAGGAGGC | 55130 |
| rs369683330 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27994393 | CCTGGCATCTGGCAG[C/G]TAATACGGAAGTACC | 55130 |
| rs369697995 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27847286 | ACGCAAATCAATAAA[C/T]GTAATCCAGCATATA | 55130 |
| rs369743074 | snp | C/G | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27959339 | GAGCTGCCCACCTCA[C/G]AGAGAGTGGTGTTGG | 55130 |
| rs369766418 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27856550 | CATCTCATCCACCCT[A/C]ATTAATGGCTTAATA | 55130 |
| rs369772637 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27823926 | CGGGCGGATCACGAG[G/T]TCAGGAGATCGAGAC | 55130 |
| rs369775521 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27893455 | ACAGCTTGTCTAAAG[G/T]CGTAGCTGGTGCTTT | 55130 |
| rs369785383 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27905748 | CTTTGACAAACCTGA[C/G]AAAAACAAGCAATGG | 55130 |
| rs369786019 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27947877 | GTGCTGAGGACTTGC[C/T]TGACTGCTATTCTTG | 55130 |
| rs369833558 | in-del | -/TG/TGTG/TGTGTG | 0.298651 | 0.24522 | intron-variant | ARMC4 | GRCh38.p7 | 10:27993974 | ATATATATATATATA[-/TG/TGTG/TGTGTG]TGTGTGTGTGTGTGT | 55130 |
| rs369880731 | snp | C/T | 1.65146e-05 | 0.0028735 | missense | ARMC4 | GRCh38.p7 | 10:27907704 | GTGCCCATGCTGCGC[C/T]GGCCTTCACGTCTGG | 55130 |
| rs369884669 | snp | A/G | 3.2963e-05 | 0.00405961 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27944834 | ACATTTGACTTCATC[A/G]GTTTCAAGCAAATTT | 55130 |
| rs369890856 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27892896 | ACTCACGCCTGTAAT[A/C]CCAGCACTTTGGGAG | 55130 |
| rs369919469 | in-del | -/TT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27910071 | CCCAAATCCCAGTCT[-/TT]ACCATTTCATATCAG | 55130 |
| rs369923176 | in-del | -/AAAC | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27910768 | TCTCAAAAAAACAAA[-/AAAC]AAACAAACAAACAAA | 55130 |
| rs369923383 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27964989 | TGGTGATAATTCCAG[A/G]AAGTGGCAGTAGCAG | 55130 |
| rs369929674 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27915211 | TCTTAAAAGCAACCA[A/C]AGAAAAAAAATGCAT | 55130 |
| rs369952558 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27837146 | GTTAAAAGACACCAG[C/G]ATCTCGGCTGCCTCT | 55130 |
| rs369955640 | snp | C/T | 3.2975e-05 | 0.00406035 | missense | ARMC4 | GRCh38.p7 | 10:27940750 | ACGTCTCTGGCCTCA[C/T]ACAGACTCGATTGGG | 55130 |
| rs369968254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27909689 | CAGGCTTGGTGGCAC[A/G]CGCCTGTAGTCCCAG | 55130 |
| rs369987648 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27949840 | GAGGGGAGGGTGACT[C/T]ATCACGAACCATAAA | 55130 |
| rs369998251 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27989196 | ATTTGTGTGTGTTAA[C/G]CCATTAGGTTTGGGG | 55130 |
| rs370059266 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27892192 | CAGAGGTCGAATCTT[A/G]GGATCTCTGTCCTTT | 55130 |
| rs370080955 | snp | A/C | | | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27996106 | CCAAGTTAGAAAGCA[A/C]GTTCTGACTTCATAA | 55130 |
| rs370102300 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27879489 | GTCTTTCCTGCTTAT[A/C]CTCAGTAACCCACAG | 55130 |
| rs370110172 | snp | C/T | 1.6501e-05 | 0.00287232 | missense, intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27971231 | CCAGAAATGTCTTTG[C/T]GGAGGGCAGCTGCTT | 55130 |
| rs370154380 | in-del | -/AGAGG | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27959177 | AGAGGAGAGGAGAGG[-/AGAGG]GGAGGGGAGTGGAGA | 55130 |
| rs370158080 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27964846 | CTGTCTTTTATACTG[A/T]CTCCCCTAGCACAAG | 55130 |
| rs370164015 | snp | A/C/G | 9.8944e-05 | 0.00703306 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27944373 | CCCCCAAGGTCAACA[A/C/G]TATTCTGTCTGATTT | 55130 |
| rs370166474 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27990960 | AGTTCTACCAGAGAA[A/G]GAAAAAAAATCAGGT | 55130 |
| rs370189374 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27969286 | GGTGTGAATCCTGCA[C/T]CCGATGCCTTCTACT | 55130 |
| rs370213670 | snp | C/T | 5.13246e-05 | 0.00506554 | intron-variant | ARMC4 | GRCh38.p7 | 10:27994911 | CTAGAAGCAAGTAAC[C/T]GGCTTACCTGACAAC | 55130 |
| rs370222446 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27969324 | TGTATCGCCGCCAAT[G/T]ATAGTTTTCTATTTT | 55130 |
| rs370224768 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27925764 | AGACACTAGAGGCAT[C/T]CCCACTAAAATTATG | 55130 |
| rs370243849 | snp | C/T | | | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:28000693 | AGAACCCACCAAGAT[C/T]TGAGCAACTATGTCG | 55130 |
| rs370292057 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27898619 | CCCCAGTTGGCTTAT[A/T]TCTTTCCCTGTAAAC | 55130 |
| rs370303230 | in-del | -/CCCC | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27850954 | AGTCTGGGAGAACCA[-/CCCC]CAGCCACTAGAGTCT | 55130 |
| rs370312052 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27891648 | TCTTATGAAAATGCA[A/T]ATATAGTTGAACATC | 55130 |
| rs370340992 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27904327 | CGCGGGGAACATGGC[A/G]TCATGGCAGGAAGCA | 55130 |
| rs370344011 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ARMC4 | GRCh38.p7 | 10:27987790 | TTTTTTTTTTTTTAG[C/T]AATTTCTTGAATTCA | 55130 |
| rs370359036 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27914241 | ACAAAATATCTAGTT[G/T]TCCAACTTTCAGCAA | 55130 |
| rs370389486 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27889492 | TAAGAAAGCTGGGTG[A/G]CCAGGCTGGAAAATG | 55130 |
| rs370418178 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27964356 | ACTTACGTGTGCCTC[A/G]GTTTCCTCACCTGCA | 55130 |
| rs370420018 | snp | C/T | 0.000153988 | 0.00877328 | missense | ARMC4 | GRCh38.p7 | 10:27987442 | GCAATAAGTAACAAG[C/T]GTGACAGCTGCCCAA | 55130 |
| rs370437913 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27887509 | CAAAACACCCCACCT[A/G]ACAACAGCAGAATAC | 55130 |
| rs370438422 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27924005 | GAAAGAAAGAAAGAA[A/G]GAAAGAAAGAAAGAA | 55130 |
| rs370461728 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27903583 | ATCTCCTTAAGCTGA[A/T]AACCAACTTCAGCAA | 55130 |
| rs370485050 | snp | A/C/T | 6.6208e-05 | 0.00575328 | synonymous-codon, intron-variant | ARMC4 | GRCh38.p7 | 10:27944285 | AAACTTGGCAACATT[A/C/T]GCGATAGTCTCGGCT | 55130 |
| rs370547662 | snp | C/T | 0.000115533 | 0.00759957 | missense, utr-variant-3-prime | ARMC4 | GRCh38.p7 | 10:27936850 | CTCCGTGCAGCCTAA[C/T]GAGGTCCCGGGTTTC | 55130 |
| rs370618097 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27967077 | CTAAGAAAGTCCTGC[G/T]CTGTCTAATTCAAAG | 55130 |
| rs370639587 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27815667 | TTCTCATCTTCTCAA[A/T]CTTCATCCATGGCTC | 55130 |
| rs370643825 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27846216 | AACAGAAATTATAAC[A/G]AACTGTCTCTCAGAC | 55130 |
| rs370648074 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27854690 | GAGCCAAGGAGGTAG[A/G]GGTTGCAGTGAGCCC | 55130 |
| rs370652115 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27864901 | ATGCAAAATGGGTAT[C/T]ATTTCCATTTTAGGT | 55130 |
| rs370673507 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27838111 | AATGCGAGCATATTT[C/T]TGGCACATTAAAAAC | 55130 |
| rs370678116 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27845089 | ATACTCCTCGAAAAG[A/C]GCAACTCCAAGACAC | 55130 |
| rs370680205 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27877375 | GTATGAGATACCAGG[A/G]GCCAAAGTCCCCGTG | 55130 |
| rs370683536 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27856945 | GCACTCCAGCCTGGA[A/C]GACAAGACCGAAACT | 55130 |
| rs370685571 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27875231 | AAGGACTTCTCTACA[C/G]TGGTTATTCTAGTTA | 55130 |
| rs370688968 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27910477 | CAGATACACTTGGGT[A/C]AGGCACGGTGGCTCA | 55130 |
| rs370698500 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27877024 | TGGGATATAGGCTCA[A/T]GTCTATCACTCAGTG | 55130 |
| rs370699691 | snp | C/T | 0.000400184 | 0.0141397 | intron-variant | ARMC4 | GRCh38.p7 | 10:27971320 | GCTAATTCCCTTTAT[C/T]TAAAAAATGAGAATA | 55130 |
| rs370702766 | snp | A/T | 0.000111489 | 0.00746539 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944177 | AGGAGCTGTGTGCAG[A/T]GGCGGCTGGCACTAG | 55130 |
| rs370799412 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27829394 | ACTCCCGTTGACTTA[A/T]CCTCATTCTCAAGGC | 55130 |
| rs370801863 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27842330 | GTGGAGAATCTCTAC[A/G]CTGTATCTTTATTTC | 55130 |
| rs370823155 | snp | G/T | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983632 | GAAGCCCATTTCTTA[G/T]CAGATTGGCTTAATG | 55130 |
| rs370845793 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27846480 | AAAGCAGGAAAGATC[C/T]AAAATTGACACCCTA | 55130 |
| rs370889470 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27850523 | TATCGTACTACTACA[C/G]TCTAGACTGGGTGAC | 55130 |
| rs370898426 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27822913 | TCCATGTTTCTTCAC[A/G]AACTTTCCACTAGAG | 55130 |
| rs370903148 | snp | A/G/T | 5.24869e-05 | 0.00512261 | intron-variant | ARMC4 | GRCh38.p7 | 10:27961764 | GCTATAGTGTGGAGA[A/G/T]CTATTAAGACCTACA | 55130 |
| rs370913598 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27851043 | TGCCTCTTGAATATT[C/T]GGCTCAGTACTGCTT | 55130 |
| rs370933762 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27829312 | TAAAGATGAAAATAA[A/C]TGACTAATTTCTTGG | 55130 |
| rs370964747 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27848542 | AACAATGGTAACAAA[A/G]GCCAAAATTGACAAA | 55130 |
| rs370987276 | in-del | -/GTATAA | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997386 | TGTCTTTAATCTTAA[-/GTATAA]CATTTGTTTTGGTAA | 55130 |
| rs370994227 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27847485 | CTGAATGGGCAAAAA[C/T]GAAGCATTCCCTTTG | 55130 |
| rs371003186 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27871287 | TAGATTGCAAAAATT[G/T]TCTCCCATTCTGTAG | 55130 |
| rs371004691 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | ARMC4 | GRCh38.p7 | 10:27987575 | AAAAATTGAAAGCTT[C/T]ATGCTACCTAGAGGT | 55130 |
| rs371016026 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27885688 | ATATATATAATATAT[-/A]ATATATAATATATAT | 55130 |
| rs371018332 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27843487 | CTTAGCACTGAGGGC[C/T]GGGCATGGTGGCTCA | 55130 |
| rs371046242 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27865161 | CAGCCTCAACTTCCC[A/T]GCCTTGACACCTCTT | 55130 |
| rs371056290 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27906061 | CAGCAAAAGAAACTA[C/T]CATCAGAGTGAACAG | 55130 |
| rs371085852 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27998463 | GCTGCAAAGGGCGGA[A/G]GAGAAAGACGGGCTG | 55130 |
| rs371122415 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27848024 | TAGATTCAATGCCAT[C/T]CCCATCAAGCTACCA | 55130 |
| rs371161786 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27990198 | TGTCACCCAGGCTGG[A/C]GTGCAGTGGCACAAT | 55130 |
| rs371164731 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27815075 | CTTCATAAACTCGAT[C/T]GAAGCCATTAGACAG | 55130 |
| rs371165427 | snp | C/G | 0.00279162 | 0.0372561 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999682 | TATTGAGGTGGGGGG[C/G]GATGGGGAAGAATGC | 55130 |
| rs371223500 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27950748 | TGCACCACCATGCCT[C/G]ACCCATATGCATTCT | 55130 |
| rs371241642 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27907106 | TGTTAAGAGAAATAG[G/T]CTCAAAAGTGATCTT | 55130 |
| rs371277296 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27966118 | TCTTACAGGTTTTTT[-/T]GGCACAGAGAGCCCC | 55130 |
| rs371281194 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27818621 | AGATTTAGAAAAAAA[G/T]CTAGTCTCCAATTGC | 55130 |
| rs371307452 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27924043 | AAGAGAAAGAAAGAA[A/G]GAAAGAGAAAGAAAG | 55130 |
| rs371333239 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27966041 | TTCCATTTTGGAGCA[G/T]AGGAAGAGGATAGGC | 55130 |
| rs371338930 | snp | A/C/T | 4.94404e-05 | 0.00497173 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27860700 | CAAGGCCTGAGCTGT[A/C/T]GCCCGATGCACGTTG | 55130 |
| rs371342087 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27982693 | CTCCAGGCAGTCCCC[C/T]GTGATGGCTGGGTCC | 55130 |
| rs371366894 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27942524 | GATATTGAATGAAGA[C/T]TTACTGTACTAGGTT | 55130 |
| rs371400775 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27955733 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTTTAATC | 55130 |
| rs371413584 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27998190 | GTTGGTAACATCCAC[C/G]GGGAGTCCGCGCATA | 55130 |
| rs371424025 | snp | C/T | 0.00158575 | 0.0281134 | intron-variant, utr-variant-3-prime | ARMC4 | GRCh38.p7 | 10:27939868 | ATGTGAGAAAGAACG[C/T]CAACAACCGCTGGGA | 55130 |
| rs371432983 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27960394 | TCTTACCTCCCAGGC[C/T]GGAGTGCAATGGCAT | 55130 |
| rs371517131 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27821345 | TATACACCCAGAGGG[G/T]CTAGGCATCTAAAGG | 55130 |
| rs371521448 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27835068 | CCGTACTTGTAGACA[C/T]CGCGTGGCCCTGCGT | 55130 |
| rs371532296 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27927302 | ACCCAAGTTTTTACC[-/A]ATAGCCACAGCCAAA | 55130 |
| rs371535051 | snp | A/G | 3.30066e-05 | 0.00406229 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944801 | CTCCGCATCCAAGGT[A/G]ACAGAGCCACTCACC | 55130 |
| rs371578704 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27855622 | CGTTTACTTGACTCA[C/G]AAACATTAACAGTAT | 55130 |
| rs371609672 | snp | A/G/T | 0.000133405 | 0.00816617 | utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27995153 | CCCATGGGATCCACC[A/G/T]TGCTCAGACCTGAGC | 55130 |
| rs371674436 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27881367 | TAAAACCCAAAGAAG[G/T]CCAGGAGTGGTGGCT | 55130 |
| rs371687867 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27938597 | TTGTATCTGTCTCTT[C/T]TTTTTTCTTTTTTTT | 55130 |
| rs371708281 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27847705 | ATCTCCTTAAGCTGA[G/T]AAGCAACTTCAGCAA | 55130 |
| rs371752746 | in-del | -/TT/TTT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27941596 | ACTGCCAGCATCCAG[-/TT/TTT]TTTTTTTTTTTTTTT | 55130 |
| rs371761494 | snp | C/G | 0.0170251 | 0.090679 | intron-variant | ARMC4 | GRCh38.p7 | 10:27845702 | CAGAGACACACATAG[C/G]ATCAAAATAAAGGTA | 55130 |
| rs371772442 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27866921 | ATCCGAACTATCTCA[A/G]TGATGTTATAGATGT | 55130 |
| rs371798118 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940978 | AAAGAAACAAAACCC[C/T]ACAAAAAACCTTCCT | 55130 |
| rs371800861 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27862378 | CATTGTTTTCATCAC[C/T]ACACCATGATATCTC | 55130 |
| rs371823397 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27865459 | CACATCTTCAGCTGC[C/T]AACTAAGGTATGCTC | 55130 |
| rs371844409 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27908780 | AAAATGTATTATTCC[A/C]AAGTTTTCAAGTAGG | 55130 |
| rs371848440 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27994215 | AAAGGCTCTAATCTG[A/C]GGACACCAGTAATTC | 55130 |
| rs371852096 | in-del | -/T/TT/TTT | 0.497211 | 0.037236 | intron-variant | ARMC4 | GRCh38.p7 | 10:27858803 | GTACACCTTAGTACA[-/T/TT/TTT]TTTTTTTTTTTTTTT | 55130 |
| rs371861001 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27897883 | GGATCTAGTTTAGAC[C/T]TTGGGGCCAAGAGCA | 55130 |
| rs371913802 | snp | C/T | 1.65078e-05 | 0.00287291 | synonymous-codon, utr-variant-5-prime, intron-variant | ARMC4 | GRCh38.p7 | 10:27981574 | GTCCCCTTCATCATC[C/T]GTTTTGCCCTTTGGG | 55130 |
| rs371924761 | snp | C/T | 8.25484e-05 | 0.00642397 | missense | ARMC4 | GRCh38.p7 | 10:27907713 | CTGCGCTGGCCTTCA[C/T]GTCTGGGTGAGGATT | 55130 |
| rs371964018 | snp | A/G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27916085 | AACCCAACGCGGGAA[A/G/T]TCAGAACCCTAGCAG | 55130 |
| rs371977694 | snp | C/T | 3.30003e-05 | 0.0040619 | synonymous-codon, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983972 | ACATCCATTTGAAAA[C/T]TCATAATCTGAAACC | 55130 |
| rs371987229 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27833063 | TCCCCCTTGCCTGGC[C/T]GTGCTTTTTGAAGTT | 55130 |
| rs371997302 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27960259 | CATTAGGGCTTGTTT[C/T]GTATAAGCTCATGTC | 55130 |
| rs372065935 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27820952 | ACACCGGCTAATTTT[G/T]CATTTTTAGTAGAGA | 55130 |
| rs372081863 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27823535 | AGGATTTTTAATAGT[A/G]CTTTCCTAATAAGAT | 55130 |
| rs372106683 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27830703 | CTCCCTGGAGCACTG[C/G]AGTGGATTGTATCTC | 55130 |
| rs372129702 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27956394 | TGGCCCTGGGAATGA[A/G]CCCTAGAGGCCTCCA | 55130 |
| rs372131381 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27885529 | AAAAAAAAAAAAAAA[A/T]AAAAATATATATATA | 55130 |
| rs372259044 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27893470 | GCGTAGCTGGTGCTT[C/T]CTTCCCTTTCATGTG | 55130 |
| rs372275699 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997746 | TAAATAAATGGTGTT[A/C]AAAAATGGTCGGCAT | 55130 |
| rs372285749 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:28001022 | GCCTCTGATTCCTGG[G/T]CTCAAGTGATCCTCC | 55130 |
| rs372337279 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27847748 | CAAAATCAATGTGCA[A/G]AAATCACAAGCATTC | 55130 |
| rs372367709 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27920242 | TTCCAATAATTTACT[A/G]ATGTGTTAATTTTCA | 55130 |
| rs372383392 | snp | C/T | | | missense | ARMC4 | GRCh38.p7 | 10:27907692 | TGCATGGACAGAGTG[C/T]CCATGCTGCGCTGGC | 55130 |
| rs372389546 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27947152 | AATACCACCAATTTT[C/T]GTACAGTTGGTTTTA | 55130 |
| rs372434058 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27960696 | TAATTGTATATTTTT[A/G]TGGGGTACAATGTGA | 55130 |
| rs372462289 | snp | G/T | 1.64868e-05 | 0.00287109 | missense | ARMC4 | GRCh38.p7 | 10:27995013 | CCTCTTGAGGATGTT[G/T]ATAGATAAAACTCTC | 55130 |
| rs372467550 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27946199 | TTAAATATATTACAT[-/A]ATAATATATAAATAT | 55130 |
| rs372511093 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27869736 | GACAGGGTTTCACCA[C/T]GTTGGCCAGGCTGGT | 55130 |
| rs372522668 | snp | A/G | 1.6477e-05 | 0.00287024 | synonymous-codon, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27936746 | AACATTCTCTTTGCT[A/G]ATGGAACATTTCCAT | 55130 |
| rs372577934 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27847992 | GTGAAAATGGCCATA[C/T]TGCCCAAGGTAATTT | 55130 |
| rs372581754 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27855524 | ACATTAAGAGTTTTA[A/T]TTAACAGGAAATATA | 55130 |
| rs372587833 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27913179 | TGCAGGTTTGTTAAA[C/T]AGGTAAATTACGTGT | 55130 |
| rs372590283 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872937 | GAAGGAATGGTCCCC[A/G]CTCCTCCTTGTACTT | 55130 |
| rs372594164 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27996658 | TTTATTACACCCTGA[A/G]TTTTCCAGAATTGTA | 55130 |
| rs372616728 | snp | A/C | 8.31428e-05 | 0.00644705 | missense, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983859 | CCATTTAAAAATACT[A/C]CTCCTGCACTGCAAG | 55130 |
| rs372647560 | snp | A/C/G | 0.000100794 | 0.00709851 | intron-variant | ARMC4 | GRCh38.p7 | 10:27907655 | ACTGACTTGCAGTCC[A/C/G]TTCTTACCTTTGCAT | 55130 |
| rs372654341 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27839577 | TACTAATGTTATTTG[C/T]CATCTAGTGCACTTT | 55130 |
| rs372655795 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27871738 | TTTGGTACCAGTACC[A/G]TGCAGTTTTGGTTAC | 55130 |
| rs372670636 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27970513 | GTCCTGACTCACCAA[C/T]TATATAAAAGTGAAT | 55130 |
| rs372675156 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27950811 | GACAGTTATTGGAAT[G/T]TTCTAGTCATTGCAA | 55130 |
| rs372688188 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27843671 | TACTTGGGAGGCTGA[A/G]GCAGAAGAATTGCTT | 55130 |
| rs372690671 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27847745 | ATACAAAATCAATGT[A/G]CAGAAATCACAAGCA | 55130 |
| rs372760438 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27838991 | ATGCCAATCTAACGC[G/T]TTTGATATCCAAACC | 55130 |
| rs372760977 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27813414 | ATAATTGGCTTAATG[A/C]TTTCTGTCCTTCTTT | 55130 |
| rs372790086 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27955555 | AACAAGGATCAAACT[A/C]CCTGCCACTCCATAC | 55130 |
| rs372790241 | in-del | -/C/CAC | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27827391 | CACTATATATATATA[-/C/CAC]TATATATATATATAT | 55130 |
| rs372845773 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27968498 | AGTTGGCCTCATATT[C/T]AATTTTTAATTGTTT | 55130 |
| rs372852340 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27951307 | AAAAATCCAAAAAAT[A/G]AGTTTTAAAAATGTT | 55130 |
| rs372893821 | in-del | -/GG | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27882281 | ATTTACTGAACAGGG[-/GG]ATAGGATTCTGGAAT | 55130 |
| rs372904098 | snp | A/G | 3.46099e-05 | 0.00415978 | intron-variant | ARMC4 | GRCh38.p7 | 10:27971352 | TTTTTAATGATATCT[A/G]AATTATCTAGTGTTC | 55130 |
| rs372924711 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27862651 | AAAGTAAAGATGGTA[C/T]CAAAACTAAACCTAC | 55130 |
| rs372974968 | in-del | -/T | 0.00874735 | 0.0655527 | intron-variant | ARMC4 | GRCh38.p7 | 10:27884199 | AACAAGGGAACCTCA[-/T]TAAGCTCAACAGCTG | 55130 |
| rs372980205 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ARMC4 | GRCh38.p7 | 10:27837002 | AGGCTCTTGAGTTGC[C/T]TTTCCAGATCCTAAA | 55130 |
| rs372982606 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27872473 | TTTTTGCCCATTCAG[G/T]ATGATATTGGCTGTG | 55130 |
| rs373007049 | in-del | -/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27884978 | CTGAGAGAAGTGGCT[-/G]GTTTCTTTAAATGCC | 55130 |
| rs373018127 | snp | A/C/G | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27949160 | TGAGCTGCCTCAAAT[A/C/G]ACTTTTGTGTTATTT | 55130 |
| rs373020064 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27957798 | TGGACGAATAATAAG[C/T]TATAGTTCATTGACC | 55130 |
| rs373033907 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983285 | CCTCTTCCCGAGGTA[C/T]GAGCATTAACTGGGC | 55130 |
| rs373056103 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27885813 | ATATAAAATATATAT[A/T]ATATATAATATATAA | 55130 |
| rs373087345 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27973532 | CTATTGCTCCCCTTT[-/T]GTGTCCATGTGTTCT | 55130 |
| rs373099838 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27835423 | TATAACAACAACAAC[C/T]GCTGCAGCAACATTC | 55130 |
| rs373118809 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27878705 | TGAAAACTGAACGGG[A/C]AAATCTTGTCGTCAA | 55130 |
| rs373126942 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27862258 | TATAGTTTAAAATAC[A/G]CTTTCACATATATTA | 55130 |
| rs373134093 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27956076 | AAAGGTGAAATCCAC[A/G]CCAGTGTTTGATGAA | 55130 |
| rs373142035 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27840753 | TTGGAAAAAAGATGC[A/T]AAAGGCTTTGGAGCT | 55130 |
| rs373161274 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27950912 | ATAATTAATTAAAAA[A/C]TAGTTCAATAAAGTG | 55130 |
| rs373251394 | snp | C/T | 1.70345e-05 | 0.00291838 | intron-variant | ARMC4 | GRCh38.p7 | 10:27860867 | CAAGGGAAAATGAAA[C/T]GGGATCTGTGCATTG | 55130 |
| rs373259459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27954841 | ATTCTTTTGTGGGCA[A/G]TATAAGCATACAAGT | 55130 |
| rs373271128 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27835072 | ACTTGTAGACATCGC[A/G]TGGCCCTGCGTCCTG | 55130 |
| rs373274785 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27978159 | CATATCCATACAATG[C/G]AATAATACACATCCA | 55130 |
| rs373285703 | snp | A/C | 0.000124386 | 0.00788527 | splice-acceptor-variant | ARMC4 | GRCh38.p7 | 10:27985212 | TGGGGTCTCTGTTAG[A/C]TGCCAAAAAAAAAAA | 55130 |
| rs373314453 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27821684 | CTTTGTCATAATTAC[A/G]TAAAAGGAATAGTTT | 55130 |
| rs373347678 | snp | C/T | 1.64953e-05 | 0.00287182 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27944338 | GTGGAGAATCAAGTA[C/T]ATTCACCATAATTGG | 55130 |
| rs373362789 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27922169 | AAAAAAAAAAAAAAA[A/G]AAAGAAAACAAAAGA | 55130 |
| rs373401168 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27885648 | TATATATTATATATA[A/T]TATATATAATATATT | 55130 |
| rs373437940 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27926939 | TACTTACAAAACAAG[-/A]AACGAAAATTCAGCA | 55130 |
| rs373440854 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27824244 | AACATCAAATCCTGC[A/T]ATGGATTGAATTTTG | 55130 |
| rs373452280 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27920732 | CTGAAAGGTCACGAA[A/G]ACTTGTTCTGTGGCA | 55130 |
| rs373458110 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27955969 | AGAGTATTGACCACT[A/C]CTAAGCTGGGATCCA | 55130 |
| rs373464599 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27846280 | AAACTCACTCAAAAC[C/T]GCTCAACTACATGGA | 55130 |
| rs373472300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983471 | TCTTTCCCTTTGTCC[C/T]TCCAACTCTTAGGAT | 55130 |
| rs373505291 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27858844 | AGTCTCGCTCTATCA[-/C]CCAGGCTGGAGTGCA | 55130 |
| rs373542350 | snp | A/G | 4.9643e-05 | 0.00498187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27934979 | CTCCCTAACACTTAT[A/G]TAAAATCTTTCCATC | 55130 |
| rs373543082 | in-del | -/GT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27955696 | CTTTAACCAATTAAG[-/GT]GTGTGTGTGTGTGTG | 55130 |
| rs373545862 | snp | A/G | 4.63768e-05 | 0.00481521 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984985 | TGCAATCTTGGCTCA[A/G]TACAATAGAGGTTCC | 55130 |
| rs373549863 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999911 | GAGGTATAGATATTT[A/G]TCCTTTGTTTTGGGT | 55130 |
| rs373551633 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27919627 | TTCACCCTATTAGAA[A/T]GACTAAATTTTTTAA | 55130 |
| rs373551894 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27905897 | ACTTAAATGTAAGAC[C/G]TAAAACCATAAAAAC | 55130 |
| rs373572317 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27915246 | CTTAGTCCCTTCAGG[C/T]TGCAATAACAGAATG | 55130 |
| rs373625443 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27934914 | ATTTTTTCATCATTC[A/G]TGCACATCAATTCTA | 55130 |
| rs373630891 | snp | C/G | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27959233 | GGAGGGGAGGGGAGG[C/G]GAGGAGGGGAGGAAG | 55130 |
| rs373639410 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27901508 | GCCCCAATTAAAAGA[C/T]ATAGATTGGCAAATT | 55130 |
| rs373644365 | snp | C/T | | | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:28000742 | CCAAGTTGCTTAATC[C/T]GATGCCAAAATGTGA | 55130 |
| rs373661709 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27943457 | TCATGATTTTATACA[A/T]TATTAAATATTATAC | 55130 |
| rs373686832 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27929394 | TGAGATGACTTTGTT[C/T]TGATTTTTGTCAGTT | 55130 |
| rs373687631 | snp | C/T | | | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27857769 | GAGGAAATTGTCTAA[C/T]AAAGCAGCTAATCCT | 55130 |
| rs373693559 | in-del | -/AAAGAA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27924048 | AAGAAAGAAGGAAAG[-/AAAGAA]AGAAAGAAAGAAAGA | 55130 |
| rs373695337 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27952868 | TATGAAACTTTTTTT[-/T]ACATAAACCAAGTTT | 55130 |
| rs373745347 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27815797 | CTGAATTCAAATGGC[A/T]TTCATATGGAACCAT | 55130 |
| rs373759617 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27882602 | TCTATTCAAGAAAAA[-/A]TGCCTGAATCTCAGT | 55130 |
| rs373768857 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27830225 | CCGGAATGTCTTTCT[C/T]ACCACATAACACCTC | 55130 |
| rs373770980 | in-del | -/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27888118 | AATAGTGCTGTGATA[-/C]AACATACAAGTACAT | 55130 |
| rs373782535 | in-del | -/AAAAAAAAAA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27909833 | AAAAAAAAAAAAAAA[-/AAAAAAAAAA]GACTCAGAACACTAC | 55130 |
| rs373830583 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27942840 | CATCTATTCATCCAT[A/C]TATCCAGCCATAAGT | 55130 |
| rs373836522 | snp | C/T | | | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27959080 | AGAGGCTCATGCCTG[C/T]AATCCCAGCACTTTG | 55130 |
| rs373848149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27853776 | ATGGGTCATAGACTA[A/G]AAGTGAAAAACCAAA | 55130 |
| rs373850960 | snp | A/G | 2.8021e-05 | 0.00374296 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944198 | CTGGCACTAGATGAC[A/G]ATGACAACATCACGG | 55130 |
| rs373874899 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27910713 | AGTGAGCCCAGATTG[A/C]GCCACTGCACTCTAG | 55130 |
| rs373921442 | snp | C/G/T | 5.00265e-05 | 0.00500112 | synonymous-codon, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27961610 | TTGCCAATATTCTGA[C/G/T]GGCAAATCTGCACTT | 55130 |
| rs373957913 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27846507 | CCTAACATCACAATT[A/G]AAAGAACTAGAGAAG | 55130 |
| rs373966793 | in-del | -/AAATAAAC | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27971004 | AATAAATAAATAAAT[-/AAATAAAC]AAACAAACAAAATAA | 55130 |
| rs374012525 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27952868 | ATGAAACTTTTTTTT[-/T]ACATAAACCAAGTTT | 55130 |
| rs374041665 | in-del | -/AAATAAACAAAC | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27971004 | AATAAATAAATAAAT[-/AAATAAACAAAC]AAACAAAATAAAATA | 55130 |
| rs374053488 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27831487 | TACTGATTCATTTGA[A/G]GTTCTCAGCAAACCT | 55130 |
| rs374106100 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27838480 | AAAGAATATATTTCT[C/T]ACAAGTTTAAAGACT | 55130 |
| rs374153843 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27825899 | TTTCTAATATATGAA[A/T]AAAATCATAACTGAA | 55130 |
| rs374155065 | snp | A/G | 0.00051213 | 0.0159938 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944790 | TGGGAACAAGACTCC[A/G]CATCCAAGGTGACAG | 55130 |
| rs374157754 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27935717 | TAAAAAAAAAAAAGT[A/C]ACTCTCAGGTATCTT | 55130 |
| rs374166770 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27820941 | CATGCGCCACCACAC[C/T]GGCTAATTTTGCATT | 55130 |
| rs374188108 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27998508 | AGGGAAGCGGCGGGA[A/G]AAGTGGAGAGCGGAT | 55130 |
| rs374190626 | in-del | -/GACT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27928728 | CATACTATGCAATCT[-/GACT]TTCATTTTCTAGTTA | 55130 |
| rs374210349 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27850663 | GAAAATATCAAAAGA[A/C]AAGACTGCCTCATGT | 55130 |
| rs374256784 | snp | A/G | 0.000264725 | 0.0115019 | intron-variant | ARMC4 | GRCh38.p7 | 10:27860607 | CTTGGACTAAACCAC[A/G]AAGTCATTCAACTGT | 55130 |
| rs374271756 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27921836 | ATAGAGCAGTATTTT[-/A]TTTTTTTTTTTGTAA | 55130 |
| rs374280364 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27888122 | AGTGCTGTGATAAAC[-/A]TACAAGTACATGTAT | 55130 |
| rs374283436 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27868157 | GCCAGTGAGAATGAC[A/G]ATCATTAAAAAGTCA | 55130 |
| rs374293344 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27871337 | GGTAGTTTCTTTTGC[C/T]GTGCAGAAGCTCTTT | 55130 |
| rs374296211 | snp | C/T | 1.65222e-05 | 0.00287417 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27862563 | TTTGTTATCTGATTT[C/T]AGTAAATTGACAATA | 55130 |
| rs374297348 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27871709 | TGTTCTGTTCCATTG[A/G]TCTATATCTCTGTTT | 55130 |
| rs374317906 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27900916 | TCCAGCAGAACTTCC[C/G]CAACCTAGCAAGACA | 55130 |
| rs374334142 | in-del | -/ATAC/ATACATAC | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27973212 | CTCATGGTCAAAATA[-/ATAC/ATACATAC]ATACATACATACATA | 55130 |
| rs374352757 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | ARMC4 | GRCh38.p7 | 10:27971093 | ATCTGAAAACAAATG[C/T]AAATATCTACATACC | 55130 |
| rs374383954 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27928083 | TCATTTATTATACAA[A/T]AAGCATTTGTCAGGT | 55130 |
| rs374388468 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27854971 | GAAAATGAAAACTTA[C/T]CTATATTGACAGAAA | 55130 |
| rs374419822 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27994065 | AACTAATACATTCTT[A/G]TACAATTATATTTAA | 55130 |
| rs374422439 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27940819 | ACCTATAATAATAGA[A/T]AAATCCAATGTTCAT | 55130 |
| rs374518294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27967379 | CACTGACAAAGTAAC[A/G]AAGGACTCCCCCGTC | 55130 |
| rs374608689 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27898186 | GACCATTGACAGTTA[A/G]TCAGTATCTATAACA | 55130 |
| rs374668149 | in-del | -/AAAAAAAAAAAAAAA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27909828 | ATTTGAAAAAAAAAA[-/AAAAAAAAAAAAAAA]GACTCAGAACACTAC | 55130 |
| rs374705044 | snp | A/C/T | 0.000101213 | 0.0071131 | intron-variant | ARMC4 | GRCh38.p7 | 10:27907654 | GACTGACTTGCAGTC[A/C/T]GTTCTTACCTTTGCA | 55130 |
| rs374705540 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27839034 | GAGGAATCCTGGACT[C/G]TTCAATTTAGGCAAG | 55130 |
| rs374725668 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27991207 | TTGCAAATGATAATA[C/T]AAAGAGACCTATGAT | 55130 |
| rs374726795 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27866930 | ATCTCAATGATGTTA[C/T]AGATGTCAATAGTCT | 55130 |
| rs374767689 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27885531 | AAAAAAAAAAAAAAA[A/T]AAATATATATATATA | 55130 |
| rs374784803 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27951702 | TGGCTTCAGAAAAAA[-/A]CCTTCCTAGTTCTTA | 55130 |
| rs374790928 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27957889 | TACTTGGAAAATGGT[A/C]AATAGAAAGTCAGGT | 55130 |
| rs374795213 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27861140 | GAGATTACAGGTGCC[C/T]GCCACCACACCTGGC | 55130 |
| rs374818412 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27896404 | ATTGAAATTCAAAGA[C/T]ATCAATGGGTAGGCA | 55130 |
| rs374828564 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27876741 | AGAAAGGAAAATATC[C/T]GGGGTCAGCTACACT | 55130 |
| rs374835758 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27865130 | CCTTTCAAGGTGCAC[C/T]CCTGGTTTATCTCTC | 55130 |
| rs374836702 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27954968 | TTTAGCTGATGGAAT[C/T]TAAATATGTTATGAT | 55130 |
| rs374843052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27906306 | CAAATCAAAACCACA[A/G]TGAGACACCATCTCA | 55130 |
| rs374881931 | snp | A/G | 4.96397e-05 | 0.0049817 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27862578 | CAGTAAATTGACAAT[A/G]AGTTCCAAACCACCA | 55130 |
| rs374883463 | snp | C/G | 1.73438e-05 | 0.00294476 | intron-variant | ARMC4 | GRCh38.p7 | 10:27862639 | TAGACAAAAATAAAA[C/G]TAAAGATGGTATCAA | 55130 |
| rs374919225 | snp | C/T | 1.691e-05 | 0.0029077 | utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27995177 | CCTGAGCTTAGCACA[C/T]GCACTACATCAGAGC | 55130 |
| rs374921183 | snp | C/T | 3.29663e-05 | 0.00405981 | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27936688 | AGGTGTTTCAGAAGC[C/T]GTATCTTCATTTCAG | 55130 |
| rs375010189 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27838403 | ATAATGGATTTTTTT[-/T]CCTGTGATAAATTTC | 55130 |
| rs375022745 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27815883 | CCAACACTTCTTAGC[C/G]ATCTCCACTTGGAAG | 55130 |
| rs375053558 | in-del | -/A | 0.00438332 | 0.0466095 | intron-variant | ARMC4 | GRCh38.p7 | 10:27953015 | ACATATAATTGATAT[-/A]AAAAAATGCACATCT | 55130 |
| rs375053618 | snp | A/G | 0.000124912 | 0.00790192 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940045 | TTATGTGTTCAAGAC[A/G]TGAATATAAGTAACT | 55130 |
| rs375150244 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27874763 | TTGTGTGTAACCCGA[A/C]CTTTCTCTCTGGCTG | 55130 |
| rs375155067 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27817280 | TTTAACTCATGATCT[A/G]TGGTTCAGAATTTTT | 55130 |
| rs375173084 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27837657 | TCTGCCAGGATTAAA[A/G]TTTAAACGTGGGTCA | 55130 |
| rs375176243 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27829202 | GATTAATATAGAAAA[A/T]ATAAAGTACAGGGCT | 55130 |
| rs375196498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27934167 | TTCCACTATAATTAT[A/G]AGGCCTCCCAGCCAT | 55130 |
| rs375212616 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27818409 | AGTCCCTGTCTTGAC[A/T]CCATTGTTATACAAA | 55130 |
| rs375241498 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27821664 | GTGAGGGCAGTTTCT[A/G]ATCTCTTTGTCATAA | 55130 |
| rs375243071 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27857245 | TTTAATAAACAGTAA[A/T]TATATTTTCTCTTCC | 55130 |
| rs375244313 | in-del | -/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27850170 | AAAACATTTGCTGGG[-/C]GTGGCGGCTCACACC | 55130 |
| rs375296067 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27941203 | AAGCCACAAGACCTG[C/T]CCAGGAACACTGGCT | 55130 |
| rs375309142 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27949726 | GTCATTTATAAAAGA[C/T]CACTCTGGCTGCAGA | 55130 |
| rs375358302 | in-del | -/ATAT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27993960 | AACTGAGGCTGGCAA[-/ATAT]ATATATATATATGTG | 55130 |
| rs375376870 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27837046 | GGATTTCTGGGACTC[A/G]TAGGAGTGTAACTGA | 55130 |
| rs375424862 | snp | C/T | 0.000297025 | 0.0121829 | missense | ARMC4 | GRCh38.p7 | 10:27995100 | TTCCAGTTCCATGTC[C/T]GGCAGCAGTCCACTG | 55130 |
| rs375457304 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27969858 | CACCTGTAATCCCAG[C/T]ACTTTGGGAGGCAGA | 55130 |
| rs375494405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27988671 | ATTGCAATGTAGATA[C/T]ATAGATGTAAAATGT | 55130 |
| rs375508125 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27963012 | TTTTGCCCTGTGTAC[-/T]TTTTTTTTTTTTTTA | 55130 |
| rs375517220 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27885656 | ATATATATTATATAT[A/T]ATATATTATATATAA | 55130 |
| rs375534660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27975227 | CTTCAAACACAAACA[C/T]GACTAGATTAAATTA | 55130 |
| rs375534822 | snp | C/T | 0.000148381 | 0.00861212 | synonymous-codon, utr-variant-3-prime | ARMC4 | GRCh38.p7 | 10:27936827 | TAGACTGGCCAAGGG[C/T]TTAAGTCCTCCGTGC | 55130 |
| rs375535760 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27812637 | GAAGCTGTCACACAT[A/G]AGGAGGAGAAGAAGG | 55130 |
| rs375575536 | snp | G/T | 0.0205511 | 0.0992634 | intron-variant | ARMC4 | GRCh38.p7 | 10:27889791 | CGTGACCTCAGTTTT[G/T]TTGGCCAATTTGAGA | 55130 |
| rs375599673 | in-del | -/ATATAA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27885691 | TATATAATATATAAT[-/ATATAA]TATATATAAAATATA | 55130 |
| rs375602405 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27933133 | CATGGTGATATAGTC[C/G]CAGCTACTAAGGAAG | 55130 |
| rs375606060 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27865274 | AATGTGATTCATTAA[C/G]TCTGGGTGAGGTCCA | 55130 |
| rs375614529 | snp | C/G | 0.00223892 | 0.0333834 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944450 | TGTGAGAAAAAAAAA[C/G]ATGAGTGGCGAATAT | 55130 |
| rs375622560 | snp | A/C/T | 0.000115357 | 0.00759385 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27812552 | GCAAGAGCCAGCCTG[A/C/T]GGATATTGGATATAC | 55130 |
| rs375638502 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984293 | TAAACTTATTTCTCT[C/G]AAATAAATGTTTAAA | 55130 |
| rs375657695 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27860282 | CATGGCAAGACCCTG[C/T]CTGTATACAAAATTA | 55130 |
| rs375667470 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27825370 | ATGTAATAAAACCTT[C/T]CTTTCTCTTCAAGGG | 55130 |
| rs375702916 | snp | A/G | 0.000131857 | 0.00811855 | missense | ARMC4 | GRCh38.p7 | 10:27940681 | ATGGCTTCTTTATTC[A/G]TATGACTCTTACTGC | 55130 |
| rs375705563 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27915084 | TTAATCCATAGGTCC[A/G]AGAAGCTCAGCGAAC | 55130 |
| rs375749098 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27921507 | ACTCATGAAGATCCA[C/T]GAATTCCAGTAATTA | 55130 |
| rs375753291 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27881456 | GCAACATAGCAAGAC[C/T]TCTGCTTCTACAAAA | 55130 |
| rs375771471 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27949587 | TAGCACCTAAATAAG[C/G]CCAGAGCCCAGGGTG | 55130 |
| rs375807618 | snp | C/T | 1.67984e-05 | 0.00289809 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940834 | TAAATCCAATGTTCA[C/T]GGAAATCTTAAAAAG | 55130 |
| rs375831721 | snp | A/G | 4.21576e-05 | 0.00459097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27971364 | TCTGAATTATCTAGT[A/G]TTCTCTGAAGATTAA | 55130 |
| rs375842956 | snp | A/G | 3.599e-05 | 0.0042419 | intron-variant | ARMC4 | GRCh38.p7 | 10:27987586 | GCTTCATGCTACCTA[A/G]AGGTCAGTAGAAGTT | 55130 |
| rs375852126 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27839862 | AGGTTGACAGTATAA[C/T]AGTACACCTCCTATA | 55130 |
| rs375859898 | snp | A/T | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27907014 | ACTTAGAGTATAATT[A/T]AAAAAAAAATTCAAC | 55130 |
| rs375891032 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27949607 | AGCCCAGGGTGGGAG[C/T]GTGGTGCAAGATGAG | 55130 |
| rs375893905 | in-del | -/AA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27941491 | CCTGCCCCCCGAACC[-/AA]AAAAAAAAGAAAAAA | 55130 |
| rs375896497 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27964035 | GAGACCAGCCTAGCC[A/G]ATATGGTGAAACCCT | 55130 |
| rs375915196 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27970366 | TCTCTATGACAGTTT[C/T]GCTGATTAGCTCCAT | 55130 |
| rs375935575 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27823846 | ACATCTCTATGTTCA[A/T]AAAAATAGTTCAGGC | 55130 |
| rs375965478 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27824490 | GACCCTTGACAGATG[C/G]TGGTGCCATGCTCTT | 55130 |
| rs375976968 | snp | C/T | 1.65712e-05 | 0.00287843 | missense | ARMC4 | GRCh38.p7 | 10:27907673 | CTTACCTTTGCATTT[C/T]TGATGCATGGACAGA | 55130 |
| rs375997606 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27927949 | TATTATACACCCAAC[A/C]CATCCCTCTAATCTA | 55130 |
| rs376024133 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27979268 | TCAGGAATCAGACAA[A/G]GATGCCTGCTTTTAC | 55130 |
| rs376037873 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27888429 | TGATTGGTGATATTG[A/C]GCAGTTTTTCATATT | 55130 |
| rs376059835 | snp | A/C | 0.000153988 | 0.00877328 | intron-variant | ARMC4 | GRCh38.p7 | 10:27860894 | ATTGTAATGACCCTG[A/C]AAGATCATGTCTATA | 55130 |
| rs376061212 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27924013 | GAAAGAAAGAAAGAA[A/G]GAAAGAAAGAAGGAA | 55130 |
| rs376100600 | snp | C/G | 0.000330322 | 0.0128473 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983997 | GAAACCAATCATCAA[C/G]CAATTAACAGGAGTT | 55130 |
| rs376103330 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27995497 | CTCCAAGAGTGGAAA[A/G]AAAAGGAAGTGGAAG | 55130 |
| rs376138848 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27832436 | TGTCACATGCTGCTA[C/G]CTGACTACTTTCTCT | 55130 |
| rs376143899 | snp | C/T | 0.000183298 | 0.0095716 | missense | ARMC4 | GRCh38.p7 | 10:27862603 | CCACCAACAAAGGAA[C/T]GAACCATTTCCCCAG | 55130 |
| rs376150944 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27980053 | AATTGATTTTCAACA[A/G]GAATGCTGAGACCAT | 55130 |
| rs376166729 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27922173 | AAAAAAAAAAAGAAA[A/G]AAAACAAAAGAAAAA | 55130 |
| rs376176962 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27871319 | TTGCCTGTTCACTCT[C/G]ATGGTAGTTTCTTTT | 55130 |
| rs376192907 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ARMC4 | GRCh38.p7 | 10:27947137 | AAAGTTACCGCCACC[A/G]ATACCACCAATTTTC | 55130 |
| rs376200446 | snp | A/G | 4.37053e-05 | 0.00467448 | missense | ARMC4 | GRCh38.p7 | 10:27985196 | CCCAGGATTTTTACT[A/G]TGGGGTCTCTGTTAG | 55130 |
| rs376224971 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27816734 | TGTAGGTCAGTATAA[A/G]ATTGTTATGCAGTTT | 55130 |
| rs376235316 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27987774 | ATAACCAAGGAAGAA[-/T]TTTTTTTTTTTTTAG | 55130 |
| rs376262277 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27948247 | TCATAGGCTTGAGGG[A/T]TTTTTTTTTAGAACA | 55130 |
| rs376279413 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27910374 | TGCAATTCCAGAGCT[C/T]GGTATTTAAATTTTT | 55130 |
| rs376279567 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27922563 | TCCTATTGATTACCA[C/T]ACAGGCAATAGATGA | 55130 |
| rs376281682 | snp | C/T | 6.61026e-05 | 0.00574865 | missense | ARMC4 | GRCh38.p7 | 10:27907766 | CGAACTCCATCTAAG[C/T]GATCAATTATCCTAT | 55130 |
| rs376283563 | snp | G/T | 1.88642e-05 | 0.00307111 | splice-acceptor-variant, intron-variant | ARMC4 | GRCh38.p7 | 10:27971315 | CTGAAGCTAATTCCC[G/T]TTATTTAAAAAATGA | 55130 |
| rs376330136 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27990809 | AGCCATTGCTCTGGT[A/G]ACCTGACTTCCTGTC | 55130 |
| rs376330781 | snp | C/T | 3.33167e-05 | 0.00408133 | missense | ARMC4 | GRCh38.p7 | 10:27994928 | GCTTACCTGACAACA[C/T]AACCTGATTCAAATG | 55130 |
| rs376332620 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27894243 | ACTTACAAAATATTC[A/G]TTGAAAATGCTAAAT | 55130 |
| rs376342980 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27921970 | TCAGGGGTTCGAGAC[C/T]CACGTGGGCAACATG | 55130 |
| rs376352176 | snp | A/C | | | intron-variant, splice-acceptor-variant | ARMC4 | GRCh38.p7 | 10:27853364 | ATGGCGAGACTCTGT[A/C]TATAAATAAATAAAT | 55130 |
| rs376355576 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27902901 | CCATTCCTTCTGAAA[C/T]CATTCCAAGCAACAG | 55130 |
| rs376386391 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27856820 | AAGAAGACAAAAATT[A/G]GTCGGGCATCATGGC | 55130 |
| rs376412283 | snp | A/G | 0.00035946 | 0.0134015 | intron-variant, utr-variant-3-prime | ARMC4 | GRCh38.p7 | 10:27939871 | TGAGAAAGAACGCCA[A/G]CAACCGCTGGGAGAG | 55130 |
| rs376424270 | snp | A/G/T | 0.000282895 | 0.0118899 | missense, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27961636 | CACTTGCTTCCTGAC[A/G/T]ATGGTCAGGTGGTTC | 55130 |
| rs376439395 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27986251 | TTTACAAAAAGAGCA[A/G]GCAGATTCTGAGGAA | 55130 |
| rs376459541 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27947933 | ATTTTCGAGCTTATA[C/T]ACTCAGCACAATCTT | 55130 |
| rs376465792 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27913456 | GTTGTTGCAAAAACA[A/T]TTACAACAGAATAAA | 55130 |
| rs376469467 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27933935 | CCCTGATAGGATTTT[A/G]CTGTGTCCCCACCCA | 55130 |
| rs376478054 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27821617 | AATGAAAGTGCAGTT[C/T]GTGTTTTCAAATCAC | 55130 |
| rs376582288 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27850954 | AAGTCTGGGAGAACC[A/C]CAGCCACTAGAGTCT | 55130 |
| rs376589795 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27846519 | ATTGAAAGAACTAGA[A/G]AAGCAGGAGCAAACA | 55130 |
| rs376597129 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ARMC4 | GRCh38.p7 | 10:27841513 | CAATTCTCCTGCTTC[A/G]GCCTCCTGAGTAGCT | 55130 |
| rs376615534 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27938663 | GAAGTCCAGTGGCGC[A/G]ATCTTGGCTCACTGC | 55130 |
| rs376619697 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27919800 | CTAATCTATAGTAAT[A/G]GAAATAAAATTGGTT | 55130 |
| rs376631473 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27832107 | AGTATTTTGAAGTTC[A/G]GATGCTTGGCGTATT | 55130 |
| rs376635011 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27979445 | ACACACACACACCCA[C/T]ACACACACACACACA | 55130 |
| rs376659988 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27890737 | TTGTTTGGACCCCTT[A/C]TGTCCCCACTTGAAA | 55130 |
| rs376689440 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27973589 | GAACAGGGGGTAATA[C/T]GTTTTCTTCTTAAAA | 55130 |
| rs376703869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27957537 | AGTAAGGTAGCTGAA[A/G]AGGGGGTTCATTGCT | 55130 |
| rs376716545 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27864562 | GAGTGAGGTGAGAGC[A/G]GGGAGTGAGGTGAGA | 55130 |
| rs376752212 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27978051 | TCATACAAATCCTTG[C/T]ACAAAAATGTTCTTA | 55130 |
| rs376820055 | in-del | -/CAAA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27947546 | CACAAAAAGAAAGAA[-/CAAA]GAAAATAAGAAAAAC | 55130 |
| rs376828578 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27969965 | ACAAAAATTAGCCAG[C/T]CGTGGTGTCACACAC | 55130 |
| rs376841852 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27894340 | TCCAAGTACACATAA[A/C]CTCCACGGATATACA | 55130 |
| rs376858999 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999799 | TCTTTTCCGGATGCC[A/G]AAGAGGCAAATGTGG | 55130 |
| rs376860257 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27979290 | TGCTTTTACCACTCT[C/T]ATTCAACATAGTCCA | 55130 |
| rs376891755 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27825636 | TTAATGAGGAGGACA[C/G]GTAAAAAGGGTTGAG | 55130 |
| rs376908802 | snp | C/T | 1.64838e-05 | 0.00287083 | missense | ARMC4 | GRCh38.p7 | 10:27935145 | ATGACTCGGTTTTCA[C/T]GTTCTTGGCAGCATT | 55130 |
| rs376915930 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27884030 | TGAAAAAATAATGGC[C/T]AAAAGTTCTCCAAAT | 55130 |
| rs376967200 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ARMC4 | GRCh38.p7 | 10:27820270 | CCTTGACCTGATGCC[C/T]GTCAAAATCTAGCCT | 55130 |
| rs376997035 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27905925 | AACCCTGGAAGAAAA[C/T]GTAGGCAATACCATT | 55130 |
| rs377014266 | snp | A/G | 9.90377e-05 | 0.00703627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944995 | CAGAGAAAGGTTAAG[A/G]AACACCGCATTCCCA | 55130 |
| rs377050064 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27925176 | TAAGAAAAACAGTAC[A/G]CTATGACTAAGTGAG | 55130 |
| rs377115270 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27870986 | ACAGTGTGAAAGTGT[G/T]CCTATTTCTCTACAT | 55130 |
| rs377120154 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27870757 | TCCACTCTATCATTG[A/T]TGGACATTTGGGTTG | 55130 |
| rs377147729 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27893610 | TTAATAAGTCTAAAG[G/T]TACTTGCAAAAGCAT | 55130 |
| rs377171808 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27866980 | AAATCACAGAACTTC[-/T]TTTTTTTTTCTCAAG | 55130 |
| rs377183334 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27883479 | ATATTGCTTTTAACA[A/G]AAAATGTGATACATA | 55130 |
| rs377191029 | snp | C/G/T | 3.31687e-05 | 0.00407228 | intron-variant | ARMC4 | GRCh38.p7 | 10:27987380 | AGACTGGAGCATTAA[C/G/T]ATCACCTTCAACACA | 55130 |
| rs377199710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27893152 | CGACAGAGCCAGACT[C/T]CTTCTCAAAAAAAAA | 55130 |
| rs377200778 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27855450 | ATATCACCTAGTAAA[A/C]TCTTCTCGGCACTCC | 55130 |
| rs377205183 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27877025 | GGGATATAGGCTCAT[A/G]TCTATCACTCAGTGA | 55130 |
| rs377214159 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27951385 | GTAATTAAAACAGCA[C/T]GTAACTAGCATGGGA | 55130 |
| rs377223404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27988415 | TGATCTCGGGTCACT[A/G]CAACCTCTGCCTCCG | 55130 |
| rs377286178 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27840688 | GAGAGGAAGCCAACT[A/G]GCATAGAAAGAATAA | 55130 |
| rs377289499 | snp | A/T | 0.000153988 | 0.00877328 | missense, utr-variant-3-prime | ARMC4 | GRCh38.p7 | 10:27936843 | TTAAGTCCTCCGTGC[A/T]GCCTAACGAGGTCCC | 55130 |
| rs377335424 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27867965 | AAAGAAAAAAAAAAA[-/A]GCAGTATAAAAAAGA | 55130 |
| rs377342895 | in-del | -/GCAATTGACATTTGGCCATTGGA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27948804 | TTTTTTTTTTTTTTT[-/GCAATTGACATTTGGCCATTGGA]TTTTTTTTTTTTCAA | 55130 |
| rs377346277 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27966471 | CCCCAAAGAAAAGCT[G/T]TCTTTTTTTTTCCAA | 55130 |
| rs377365689 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27885821 | TATATATTATATATA[A/T]TATATAAATATATAT | 55130 |
| rs377390459 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARMC4 | GRCh38.p7 | 10:27978649 | AATACAAAATTAGCC[A/G]GGTGTGGTGGTGTGC | 55130 |
| rs377434173 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27891691 | ATAAAAACTTTTAAA[A/G]ACTCATTAATGAAAG | 55130 |
| rs377476849 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27972057 | CATTCTAACATATAA[C/T]TGACTATCTAAAGCA | 55130 |
| rs377478323 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27989844 | ACAGAGTGAGACCCC[A/C]TCTCAAAAAATAAAA | 55130 |
| rs377478647 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27908371 | TAAAGACACTGTAAT[C/G]AAAATAGCTTCATGA | 55130 |
| rs377482433 | in-del | -/TGAC | 0.00914312 | 0.0669923 | intron-variant | ARMC4 | GRCh38.p7 | 10:27841096 | ATGAGCTATTTATAT[-/TGAC]TATTTGCTAGTGTAA | 55130 |
| rs377482668 | in-del | -/AAAG | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27882174 | CCTTGTCATAAAAAA[-/AAAG]AAAGAAAGAAAGAAA | 55130 |
| rs377495121 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27952579 | CAGGCCCTGGTGTGT[A/G]TTGTTACCCTCCCTG | 55130 |
| rs377506117 | in-del | -/AA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27885646 | ATATATATTATATAT[-/AA]ATTATATATAATATA | 55130 |
| rs377518709 | snp | C/T | 6.83247e-05 | 0.00584446 | intron-variant | ARMC4 | GRCh38.p7 | 10:27961732 | TAAGAACAATAACAA[C/T]ACACATACACATGTA | 55130 |
| rs377520660 | snp | A/C | 0.000356201 | 0.0133407 | intron-variant | ARMC4 | GRCh38.p7 | 10:27936925 | GTCATCAAGGAATAT[A/C]AAGCTTTCAATGATG | 55130 |
| rs377537419 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27894890 | TTTTTGTTTCACTCA[A/G]CCTCACTGTTCCTTA | 55130 |
| rs377540384 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27963424 | AAGAGGAGAAAAAAA[-/A]TCATTCACTTTGAAG | 55130 |
| rs377541078 | in-del | -/TATAT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27885733 | ATATTATATATAAAA[-/TATAT]TATGTTATATATAAT | 55130 |
| rs377545802 | snp | C/G/T | 8.30884e-05 | 0.00644504 | intron-variant | ARMC4 | GRCh38.p7 | 10:27907790 | ATCCTATCGTGGAAC[C/G/T]CAAAATCATGATATA | 55130 |
| rs377565587 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27842666 | TAGAAGCCAAAAATA[A/T]TTCCCCACAGTAAAA | 55130 |
| rs377571665 | snp | C/T | 1.65608e-05 | 0.00287752 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27944281 | TTTTAAACTTGGCAA[C/T]ATTCGCGATAGTCTC | 55130 |
| rs377577808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27977428 | AAAAATTAGCCAGGC[A/G]CGGTGGCGGGCGCCT | 55130 |
| rs377579857 | snp | G/T | | | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999137 | CCTCCCGGGAAACAC[G/T]TTTATTCAACTTTGC | 55130 |
| rs377613170 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27990924 | CAATATTATAGCACA[C/T]TTGATTCAAAATCAT | 55130 |
| rs377629180 | in-del | -/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27852981 | AAAAAAAAAAAAAAA[-/G]AAAAGCTAACCGTGT | 55130 |
| rs377639755 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27817220 | CATGGCTTACATGTC[C/T]TTGTATAGCTATTCA | 55130 |
| rs377677413 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27890763 | TGAAAATCTGGTATA[C/T]ATATATTTAAAAAAA | 55130 |
| rs377679587 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27879768 | ATAAGAGTCTACTAA[C/G]TCATAATGAATGTAA | 55130 |
| rs386371018 | in-del | -/TT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27859057 | AATTTTATAGTTTCT[-/TT]TTTTTTTTTAAGACT | 55130 |
| rs386371019 | in-del | -/TT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27859065 | AGTTTCTTTTTTTTT[-/TT]TAAGACTGCATACTT | 55130 |
| rs386371020 | in-del | -/AAA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27895042 | TAGTCATCGGTACGA[-/AAA]AAAAAAAAAAAAACT | 55130 |
| rs386371021 | in-del | -/AAA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27895053 | ACGAAAAAAAAAAAA[-/AAA]AACTGTTAGCTCTTA | 55130 |
| rs386371022 | in-del | -/AA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27935703 | TGTGCTACTTGGATA[-/AA]AAAAAAAAAAAGTCA | 55130 |
| rs386371023 | in-del | -/AA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27935713 | GGATAAAAAAAAAAA[-/AA]AGTCACTCTCAGGTA | 55130 |
| rs386371024 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27941506 | AAAAAAAAGAAAAAA[-/A]AAAAAACCATGAGAT | 55130 |
| rs386371025 | in-del | -/TA | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27982173 | ACAGAATATATATAT[-/TA]ATAATGTATACACAC | 55130 |
| rs386371026 | in-del | -/GT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27993994 | GTGTGTGTGTGTGTG[-/GT]TGTGTGTGTGTGTGT | 55130 |
| rs386742293 | multinucleotide-polymorphism | AA/GG | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27836053 | AGCCTGAAGAGGAGG[AA/GG]GAGGAAGAGGGGTTG | 55130 |
| rs386742294 | in-del | AG/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27888127 | TGTGATAAACATACA[AG/C]TACATGTATCTTTTT | 55130 |
| rs386742295 | multinucleotide-polymorphism | CC/TT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27901543 | AAAGATCAAGACCCA[CC/TT]GGTGTGCTGTATTCA | 55130 |
| rs386742296 | multinucleotide-polymorphism | AAAAAACCAAACACCGCATGTTCTCAT/GAAAAACCAAACACCGCATGTTCTCAC | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27906765 | AACTAATACAGGAAC[lengthTooLong]TCATAAGCGGGAGTT | 55130 |
| rs386742297 | multinucleotide-polymorphism | ACG/GCA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27945002 | AGGTTAAGGAACACC[ACG/GCA]TTCCCATAGAAATGC | 55130 |
| rs386742298 | multinucleotide-polymorphism | CA/TG | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27957480 | GTAAGACAGACAACC[CA/TG]AACCATCAGGATAGC | 55130 |
| rs386742299 | multinucleotide-polymorphism | CAA/TAT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27961157 | ATATTAATTTTATTC[CAA/TAT]GGGTTGAGAAAATTA | 55130 |
| rs386742300 | in-del | AATAATAGACTAT/TTATATGAACTTGTTGCTAAGACC | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27963637 | GGCCTTATATGAACC[lengthTooLong]TTATGGTCTTAATTC | 55130 |
| rs386742301 | in-del | AT/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27976214 | GACCATTTCTATTCA[AT/C]TTTTTACTGGTGATT | 55130 |
| rs397695921 | in-del | -/T | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27869552 | TTTCTTTTTTTTTTT[-/T]GAGATGGAGTTTCAC | 55130 |
| rs397697192 | in-del | -/TTT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27941616 | TTTTTTTTTTTTTTT[-/TTT]GCAATAACTAAAGTC | 55130 |
| rs397699788 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27974703 | GTTTTTTTTTTTTTT[-/T]GCTTAGGATTGCCTT | 55130 |
| rs397716927 | in-del | -/A | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27923040 | CCACTAGAACAAAAA[-/A]TGCAAACCTTTCTAA | 55130 |
| rs397719025 | in-del | -/A | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27977417 | AAAAAAAAAAAAAAA[-/A]TTAGCCAGGCGCGGT | 55130 |
| rs397725134 | in-del | -/TT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27859066 | GTTTCTTTTTTTTTT[-/TT]AAGACTGCATACTTA | 55130 |
| rs397726027 | in-del | -/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27963815 | GTTTTTTAGACCCCC[-/C]ATGCATTTGGCCACA | 55130 |
| rs397737939 | in-del | -/AA | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27935714 | GATAAAAAAAAAAAA[-/AA]GTCACTCTCAGGTAT | 55130 |
| rs397738310 | in-del | -/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27903551 | ATATTTAGAAAACCC[-/C]ATCGTCTCAGCCGAA | 55130 |
| rs397739756 | in-del | -/GT | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27862802 | ATAAAGTGTGTGTGT[-/GT]ACATATGTATAAGTC | 55130 |
| rs397743829 | in-del | -/A | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27926024 | AAAAAAAAAAAAAAA[-/A]GTAACACTTTCTCTA | 55130 |
| rs397746063 | in-del | -/TA | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27982176 | GAATATATATATATA[-/TA]ATGTATACACACATC | 55130 |
| rs397755365 | in-del | -/T | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27862681 | CATTTAGGCATTTTT[-/T]AAGAGGCAGAAAGTA | 55130 |
| rs397762503 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27908768 | ACCAGGGGGGAAAAA[-/A]TGTATTATTCCAAAG | 55130 |
| rs397763673 | in-del | -/G | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27966133 | GGAAGTGCAAAAATT[-/G]GGGGCTCTCTGTGCC | 55130 |
| rs397781109 | in-del | -/A | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27922168 | AAAAAAAAAAAAAAA[-/A]GAAAGAAAACAAAAG | 55130 |
| rs397793645 | in-del | -/A | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27829944 | ATTAAAAAAAAAAAA[-/A]TGTAAGCAGTGGAAC | 55130 |
| rs397804418 | in-del | -/A | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27925003 | AAAAAAAAAAAAAAA[-/A]TCCCGATTCCTTTTG | 55130 |
| rs397826192 | in-del | -/T | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27948256 | GAGGGATTTTTTTTT[-/T]AGAACAGTTTTATAT | 55130 |
| rs397830309 | in-del | -/A | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27833387 | AAACTGAAAAAAAAA[-/A]TCAAGGAGGAAAATT | 55130 |
| rs397841531 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27907902 | AATTTTTTTTTTTTT[-/T]GCAAAACTTCATCAA | 55130 |
| rs397844025 | snp | C/T | 0.21875 | 0.248039 | intron-variant | ARMC4 | GRCh38.p7 | 10:27966795 | ATACTTTCGGCCCAA[C/T]ATCTGTTTCAGGAAA | 55130 |
| rs397844629 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27993243 | TTTTTAATTTGTTTT[-/T]ACGTAGGAGATCATA | 55130 |
| rs397844761 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27941338 | GAAAAAAAAAAAAAA[-/A]GCTGGATGTGGTGGT | 55130 |
| rs397846568 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27977416 | AAAAAAAAAAAAAAA[-/A]ATTAGCCAGGCGCGG | 55130 |
| rs397965573 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27838762 | ACTTTATTTTACCAT[-/T]ACTGTTTGTGTATTT | 55130 |
| rs397973161 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27907902 | ATTTTTTTTTTTTTT[-/T]GCAAAACTTCATCAA | 55130 |
| rs398013099 | in-del | -/TCATTCAT | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27954523 | CCCTTAAGCTTCAAC[-/TCATTCAT]TCATTCATTCATTCA | 55130 |
| rs398075032 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27833386 | CAAACTGAAAAAAAA[-/A]ATCAAGGAGGAAAAT | 55130 |
| rs398096858 | in-del | -/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27858655 | ACTGTGTGGGTGGGC[-/C]AAACACAGTTTGGTC | 55130 |
| rs398096859 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27907503 | CTGACCAGAAAAAAA[-/A]GCAATGCTCCGAAAT | 55130 |
| rs527240361 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27837680 | GTGGGTCATAAAGAA[C/T]GACAAAATAAACTTT | 55130 |
| rs527247466 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27953727 | ATAAATTATATATGT[A/C]TATAAACAGAGAAAC | 55130 |
| rs527249316 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27827494 | CCCCCCACAAGCAGA[C/T]TTCTTCTCTCCTCCT | 55130 |
| rs527250123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27946387 | AGGTCAAGTTTTTAA[C/T]TTTTAAAAATTTATA | 55130 |
| rs527276511 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ARMC4 | GRCh38.p7 | 10:27852790 | ACATGGCAAAACCCC[A/G]TCTCTGCTAAAAATA | 55130 |
| rs527287345 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27946950 | CAACAACTGTCCCGT[A/G]AAGATGTCACTGACA | 55130 |
| rs527298316 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27864831 | TCCCAACGGCGTATC[A/G]GGCATGGTACTACGC | 55130 |
| rs527300037 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27834789 | TAGTGATTCTCTCTT[C/T]TAATTCTCAGATGTC | 55130 |
| rs527313059 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27859602 | AGATGTAAATGCATC[G/T]GGTTGTCATAGGCTC | 55130 |
| rs527314159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27867681 | AGGGCTGGGTGCAGT[A/G]GCTCACGCCTGTAAT | 55130 |
| rs527327175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27906860 | ACACATCGGGGCCTG[C/T]CAGGGGGTGCGGGAC | 55130 |
| rs527335200 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27995916 | AGTTAATGTGAGAGA[A/T]GTAGGAATAAGTGAG | 55130 |
| rs527341699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27901034 | CAGCAAGATTGAAAT[A/G]GAGGAAAAAATCTTA | 55130 |
| rs527347361 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27867243 | AACCCCAAAGGGCCA[C/T]GAAGTTCTCACTGGA | 55130 |
| rs527360742 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27928622 | TTGCCATTTAAGGCC[C/G]CTTGTTTCAATTTAT | 55130 |
| rs527361052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27819328 | GAGTTTGAGGGGTTT[A/G]GAGTAGAAAGATTAT | 55130 |
| rs527361372 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27959773 | AATAATGAATGCCTA[C/T]AATAGTAGTGAATCA | 55130 |
| rs527386357 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27959511 | AGCTGGGCATGGTCA[C/G]CGTGCGTGCCAGTCT | 55130 |
| rs527395523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27995265 | GACTTTAAACTAGTA[C/T]TCCCCATCCCACATT | 55130 |
| rs527398229 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27826428 | CAACTTTCTCCACAG[C/G]AGCTATTTAAAACCG | 55130 |
| rs527410892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27960083 | TTTATAAAGTATCAC[A/G]CTTAAAATGAAATTT | 55130 |
| rs527424544 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27953123 | AATAAATATATCCAT[A/C]ACCTGAAAACATGTC | 55130 |
| rs527437316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27833149 | GCTATATGGCCATGA[C/T]ATATTTAGAGGTGAC | 55130 |
| rs527478338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872670 | CGTTTATTGATTTGC[A/G]TATGTTGAATCAGCC | 55130 |
| rs527484305 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27918153 | AAACAAAGAGAAAAA[A/G]TAATTTCTCAACTTG | 55130 |
| rs527540247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27933296 | TGTAACTCCAGACAA[C/T]TGATATTTGCAAGTA | 55130 |
| rs527553791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27925551 | TTTGTAGAGACAGGG[C/T]CTCATTACGTTTTCC | 55130 |
| rs527563441 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27878103 | ACTTAGGAGATTAGT[A/C]ATTTTAAAAAAAGAT | 55130 |
| rs527582030 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27832634 | GGCGGGCTCCTTTTG[G/T]TGTTACTGGTTAGCA | 55130 |
| rs527594706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27973228 | ATACATACATACATA[C/T]ATACATACATACATA | 55130 |
| rs527596889 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27965306 | CCATGCCCTGTGGTT[A/C]CACAGAGCCTAGGGA | 55130 |
| rs527597823 | in-del | -/TAT | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27887571 | CCAGGATAGACCATA[-/TAT]GAAGCCGCAAAACAA | 55130 |
| rs527648583 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ARMC4 | GRCh38.p7 | 10:27846007 | CTGTCAACATTAGAC[A/G]GACCAATGAGACAGA | 55130 |
| rs527664515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27939465 | TTATGCCTGTAATCC[C/T]AGCACTTTGGGAGGC | 55130 |
| rs527673348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27966002 | CCCAGTGGGTTCTCG[C/T]CCATAAAAGTCTTTT | 55130 |
| rs527709664 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27932594 | AGGTGGTTTCTCAGG[C/T]GAAGCCCAGTTCCAT | 55130 |
| rs527765135 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27877229 | AGTTGACCTCACAGC[A/G]ACTAATGACTTCCCA | 55130 |
| rs527767155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27905544 | ATGGAACCAAAAAAG[A/G]GCCTGTATAGCCAAG | 55130 |
| rs527767974 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27893979 | ACAGAGCAAGACCCT[A/G]TCTTGATCTGAAAAA | 55130 |
| rs527771521 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | ARMC4 | GRCh38.p7 | 10:27812111 | GACAGGACAGTTAGA[C/T]TGGTTTAACAGAAAG | 55130 |
| rs527826122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27850631 | GCCCTAACTTTCTAT[A/G]AATTTATTCTCTAAG | 55130 |
| rs527829337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27858752 | TAATTGCGAGTTGCA[C/T]ATACACCAGGCATTT | 55130 |
| rs527833475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27938711 | TTCAAGTGATTCTCC[C/T]GCCTCAGCCTCCTGA | 55130 |
| rs527863561 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ARMC4 | GRCh38.p7 | 10:27858087 | TGCATTACCTGGCTC[G/T]TGAAATCTTCCTCTT | 55130 |
| rs527875866 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999683 | ATTGAGGTGGGGGGG[G/T]ATGGGGAAGAATGCA | 55130 |
| rs527899122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27864854 | TACTACGCACTTCAC[A/G]TAAGTTATTTCAGTT | 55130 |
| rs527901074 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27905875 | ATTAACTCAAGATGG[A/T]TTAAAGACTTAAATG | 55130 |
| rs527944803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27917216 | TTAAACTAGAAATCA[A/G]TAACAACATGGGATC | 55130 |
| rs527950504 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27871284 | GAGTAGATTGCAAAA[A/T]TTGTCTCCCATTCTG | 55130 |
| rs527956643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27817628 | TCACTTAGGATAAGG[A/G]CCTCCAGTTCCATTT | 55130 |
| rs527977651 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27964390 | TGGGGATGATAATAG[A/C/T]AATTAGTATGTAAAA | 55130 |
| rs528003489 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27957972 | TAAATTAAAATGTCA[C/G]GTGTATTTATTTTGA | 55130 |
| rs528029761 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27831442 | GAGTGCTTACCATGT[A/T]TCAGGCACTACTCAA | 55130 |
| rs528086824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27870925 | GATCCTTGAGGAATC[A/G]CCACACTGTCTTCCA | 55130 |
| rs528100326 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27956754 | TTGAAATGGATTTCA[A/G]CGTGTTTTTGACCTT | 55130 |
| rs528102339 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27924430 | CTTTTATTATTTTTT[A/T]AAAAATTAAAATAAT | 55130 |
| rs528110090 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27916382 | AGATGGGGATGATTA[A/T]GAAAGCTTGGTTACA | 55130 |
| rs528110222 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27853135 | GCACTTTGGGAGGCC[A/G]AGGCCGGCAGATCAC | 55130 |
| rs528125448 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27876832 | ATGTTCCCTGATGAA[A/C]TTCTTGAGCTGCAGA | 55130 |
| rs528145488 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27884415 | AATTTCCTGGCACTT[A/T]TATTTGCACTTTCTC | 55130 |
| rs528160808 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27920869 | AAAACTGAAAAAAAA[-/G]AAACTATGTAAATGC | 55130 |
| rs528166714 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27837366 | GCAAAATGGAATGAA[C/T]GAAAATATCAGGTTG | 55130 |
| rs528198747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27883525 | GTATGCCTCAAAGTA[C/T]GCACCAGAGGAAAAA | 55130 |
| rs528219631 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27836898 | TCATAAACATCAAAC[A/C]TAAAGAGTATAGCTC | 55130 |
| rs528225360 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27899291 | CTGGCCCAGATACTA[C/T]ACTTTTCCCACGGTC | 55130 |
| rs528227005 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27844846 | GGAGGAAAATTTATT[C/T]GGCTAGCGATGGGGT | 55130 |
| rs528266025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27844297 | AAAAGAGAAATGGAG[C/T]CCTTGGGATGGATTT | 55130 |
| rs528266120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27850135 | TAGTTTCCTCGTCTG[C/T]GAACTGTGTGTTTAA | 55130 |
| rs528275976 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27937133 | AAGCCAGTTTTGAGA[G/T]AGCCTAGGCATCTCC | 55130 |
| rs528299194 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27937567 | TTGAAATAAATATTT[A/C]CTGCACAGATGGTCT | 55130 |
| rs528306704 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27844615 | TCTTTATGAAACTCA[A/G]TTTCTTTATCTGTAA | 55130 |
| rs528310690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27930890 | ATCTCTAAAAGTTTA[C/T]AGTTTCTTTTTGTGT | 55130 |
| rs528333588 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27977445 | GGTGGCGGGCGCCTG[C/T]AGTCCCAGCTACTTG | 55130 |
| rs528361377 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27817057 | GCCCGGCCTGTTATG[C/T]AGTTTTATACATACA | 55130 |
| rs528361881 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27987250 | TTTTCATGAAGTTGT[A/C]CATTTGACTTTTTAC | 55130 |
| rs528371527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27992386 | TCAGGAGGGAACACT[A/G]TGCATAAAGACTGCA | 55130 |
| rs528374258 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27983004 | TAGAATCAGCTAAAG[A/G]AAGACTGAAAGGCTG | 55130 |
| rs528395584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27816811 | TGGAGTGAAGTGGTG[C/T]CATCTTGGCTCACTG | 55130 |
| rs528422766 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27856535 | ACTCTCTGCCAAAAA[C/T]ATCTCATCCACCCTC | 55130 |
| rs528439175 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27956558 | TCCTGTAGTGACAGC[G/T]CTAGGAAATATCTTC | 55130 |
| rs528444242 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27943644 | ATATAAAAATTGGCC[A/G]GGCTTGATGGCGGGC | 55130 |
| rs528447089 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27815964 | TTCTATATAAACATG[A/T]ATCTCTTTCCAAGTA | 55130 |
| rs528456455 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997902 | AGTAAAGAAAGTAAG[A/T]TTAAAGATTAAAAGG | 55130 |
| rs528490352 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27870200 | CATGACATTCAGGCA[C/T]TTCCCGATCTGGCCC | 55130 |
| rs528509040 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27903341 | AACCCACAGCCAATA[C/T]CATACTGAATGGGCA | 55130 |
| rs528558149 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27841898 | TAGCTGGGACTACAG[A/G]TATGCACCACCATGC | 55130 |
| rs528579763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27976948 | CACAGACAAATGAAC[A/G]ACTAATTTTTGACAA | 55130 |
| rs528589584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27908907 | TCTTAAAAAGGACTT[C/T]TAATAAGAAAAAATA | 55130 |
| rs528605442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27963101 | CAACCTCCGCCTGCC[A/G]GGTTCATGTGATTCT | 55130 |
| rs528614137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27969386 | CCTGCACCTGGTTTT[C/T]CAGGTATTCGCAGGC | 55130 |
| rs528631772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27830167 | TGTTCATCTTCATAA[C/T]AGGAGTGGAGCCTAA | 55130 |
| rs528647548 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27835898 | ACCACTGCACTCCAG[C/G]CTGGGTGACAAGAGT | 55130 |
| rs528667442 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27829493 | GCTACCAATTTGAGG[A/C]ATGTTTTCCTTGTCT | 55130 |
| rs528667800 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27948116 | TTTTGAAGTATCTCT[A/G]GGTTAATTTGGAATG | 55130 |
| rs528687580 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27921657 | TTGTATAAATTATAT[G/T]TCAGGTTGACAAACA | 55130 |
| rs528693133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27835447 | AACATTCAGATACAC[C/T]CACTGTGAGGCAGGT | 55130 |
| rs528714679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27882253 | ATGAACTCTCTGATC[C/T]CATTCTCAATAAGAT | 55130 |
| rs528772565 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27969055 | TATTAGCTTTATTGC[C/T]TTATGCTAATTAATA | 55130 |
| rs528778449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27976609 | CTAAGACCTAAATAA[A/G]TGGAGAGACATACTA | 55130 |
| rs528789542 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27915302 | ACACACATTTATTTC[A/T]CACAGTTCTGGAGGC | 55130 |
| rs528791526 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27890315 | ATCACGACAGCATGC[A/G]TTGTTTGATGCTGGG | 55130 |
| rs528807965 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27950404 | ACACTGATGACTTAG[A/C/G]ACTCAAAAACCTAAG | 55130 |
| rs528811196 | in-del | -/AAAGAAAT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27882230 | AAGAAAGAAAGAAAG[-/AAAGAAAT]ATGAACTCTCTGATC | 55130 |
| rs528822545 | snp | A/G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27922675 | CTTTGGAAGGCCGAG[A/G/T]TGGGTGGATCATTTG | 55130 |
| rs528833549 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27824841 | TTTGGAAATAGATTT[A/C]TTGGGGAAAGGTTGT | 55130 |
| rs528838213 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27856174 | TCACAAATTTGTAAT[A/G]ATACAAATCCCTGGG | 55130 |
| rs528853359 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27889518 | AAATGGAGAGGGATT[C/T]CTGAATTCCACTGTC | 55130 |
| rs528856472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27917408 | ACCTTTAAAAAATTA[C/T]ATAAGACAAGAATTG | 55130 |
| rs528866205 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27964950 | ACTTCAGTCTAGGTT[A/T]AGATTTTGGAAGAAG | 55130 |
| rs528873666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872066 | CTCCTTGAAGAGTAC[C/T]TTCACATCCCTTGTA | 55130 |
| rs528894113 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27910904 | AAAGTGGGTTCCCGT[C/G]AGCCTCTAGTCAGAA | 55130 |
| rs528909671 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27874185 | ATTGCAACCCCTGCC[-/T]TTTTTTGTTTTCCAT | 55130 |
| rs528920040 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27918378 | CCTTCCAAAACAAAT[A/C]ATGGTGAGTCACTTT | 55130 |
| rs528939805 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27924658 | GAAGAAAGCCCACAT[C/T]ATACAAAAATTTAAA | 55130 |
| rs528975652 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27859283 | GCTTTGGCCAGATTT[C/T]TGCTTGAAGAAACTA | 55130 |
| rs528977960 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27829253 | TCTTCTTCGATGTCA[A/G]ATAAATAGCTTTCCC | 55130 |
| rs528990708 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27937055 | AGCTTTCTGACAGCA[C/T]GTCTCTCTCCTTATG | 55130 |
| rs529024372 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27838018 | CCTAAGAATCTAAGA[C/T]TTTTGTATTTTTTTA | 55130 |
| rs529032986 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27964488 | ATTCATTCACCAAAC[G/T]TGCATGGAGGGCCTG | 55130 |
| rs529042654 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27971023 | AAACAAACAAACAAA[A/C]TAAAATAAAATAAAG | 55130 |
| rs529062488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27837425 | GTGATCATCTAAGAA[A/G]AAATACCTTAGAAAC | 55130 |
| rs529081248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27938554 | CCTCCCTCACAACCT[A/G]ATACAATCCTCTACT | 55130 |
| rs529081726 | in-del | -/AG | 0.00835141 | 0.0640778 | intron-variant | ARMC4 | GRCh38.p7 | 10:27957215 | ACGGCAGGAAAAGGA[-/AG]AGAGAGAGGGATGCA | 55130 |
| rs529087744 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27964037 | GACCAGCCTAGCCAA[C/T]ATGGTGAAACCCTGT | 55130 |
| rs529094436 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27884533 | AGTTGCTTGCCATGT[A/T]TTGGCCTATCTGTGG | 55130 |
| rs529094657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27893726 | TAGGACAGGGGCAGT[A/G]ACGGGGAGAAAGAAA | 55130 |
| rs529097496 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27936240 | AAATCAAATGGTCAT[A/G]AAGGTTACAAATACT | 55130 |
| rs529100573 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27884500 | TTTCCTTCCTTCAGC[C/T]GGAAGGACCAAAGTG | 55130 |
| rs529123426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27931901 | ATGGGGTTATGTCCC[A/G]ATAAACCCATCATAA | 55130 |
| rs529131566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27893153 | GACAGAGCCAGACTC[C/T]TTCTCAAAAAAAAAG | 55130 |
| rs529137972 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27985671 | CCAAAATAGCATGCT[G/T]TCCTAAGCCTACAGA | 55130 |
| rs529170066 | in-del | -/CGCCGC | 0.302686 | 0.244385 | upstream-variant-2KB, intron-variant | ARMC4 | GRCh38.p7 | 10:27998930 | GTGCCCTCCCCCGGG[-/CGCCGC]CGCCGCCGCCGCCGC | 55130 |
| rs529188489 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27912324 | CTTTCAAGATCTTCA[G/T]TTTTATCTCAGAAAT | 55130 |
| rs529221403 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27850171 | AAACATTTGCTGGGC[C/G]TGGCGGCTCACACCT | 55130 |
| rs529248266 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27993722 | CAATAGAAGAATTAA[A/C]GAGCTTTTGAAATAC | 55130 |
| rs529249684 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27937650 | AGACTTGGCAATTAC[G/T]CCAAGCACACAGATG | 55130 |
| rs529260326 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27824385 | TGCTGTTACAGGGGG[A/G]TTGGGCTCCTAATAA | 55130 |
| rs529271658 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27864028 | ATTTTTATCAATTTT[A/T]TATCTTAGAAGATTT | 55130 |
| rs529273520 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27943830 | AAAAAAAAAAAAAAA[G/T]GCATCATAGATGTCA | 55130 |
| rs529285166 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27902898 | GGACCATTCCTTCTG[A/T]AACCATTCCAAGCAA | 55130 |
| rs529288662 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27850897 | GGAGGGAGAGCCCAG[A/G]CAAAGCCTGACAGTC | 55130 |
| rs529297149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27992561 | CAGGCATAGTAGTAT[A/G]TGCCTATAGTCCTAG | 55130 |
| rs529315469 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27904237 | CTAAAGCCTTCCAGA[C/T]TTTCTGTAAGAAGTG | 55130 |
| rs529320177 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27867880 | CTTGAACCTGGGAGG[C/T]AGAGATTACAGTGAG | 55130 |
| rs529323457 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27821021 | CTGATCTTAAGTGAT[C/T]TGCCCACCTCAGCCT | 55130 |
| rs529335573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27898934 | TCGCTTTTTAAAAAA[C/T]ATTATATTTAGGATG | 55130 |
| rs529360321 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27998557 | GAGGTAGTGCAGAGA[A/G]GGGCGCAGGGACTGA | 55130 |
| rs529362451 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27962375 | GCCTCGTGGTTACCA[C/T]ACTGGACAGCTCAGA | 55130 |
| rs529377857 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ARMC4 | GRCh38.p7 | 10:27957410 | CACACTAGCAAGATG[C/T]CCTGCGAGATACAGC | 55130 |
| rs529379464 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27999016 | TCGGGACCTCCGCGC[A/C]TCCAAGATTCCCGCG | 55130 |
| rs529381772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27823300 | TAAAAAAATCTATGT[A/G]GATAAGATTGTTTAG | 55130 |
| rs529404518 | snp | C/T | | | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999772 | TGGGGTGTTTAGGAA[C/T]TAAAACTGGATTCTT | 55130 |
| rs529418742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27963183 | TGGCTAATTTTTGTA[C/T]TTTTAGTAGTGACGG | 55130 |
| rs529419289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27830901 | ACTTCTGGCAAGATT[C/T]TTTAAATAATTGTTT | 55130 |
| rs529436529 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27870238 | ATCTTTTCTCTCCCA[A/G]TCTCAATCTTTTCTC | 55130 |
| rs529438975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27822667 | TCACATGACAGCTCA[C/T]CAAAGCCGGGGGCCT | 55130 |
| rs529467364 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27905061 | TGCTGAGGCTTGAGC[A/G]CTGAGCCCAGCTGCA | 55130 |
| rs529483083 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27917775 | TTAGCTCACAGATTA[-/T]TTTTTTAATGGACCA | 55130 |
| rs529492564 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27875901 | CCAGGAGATTATATC[A/G/T]CACGCCTGGCTCGGA | 55130 |
| rs529509979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27914951 | TGTCTGTGAAATATT[A/G]TTAAATGAAACAACA | 55130 |
| rs529539142 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27969472 | ATGCTTGAAAGAGTA[A/C]GAATATGGAAAAAGC | 55130 |
| rs529544323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27963830 | CATGCATTTGGCCAC[A/G]AGAGTTCCGGACAAC | 55130 |
| rs529549006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27922254 | AGGCTGTCCACTGAG[C/T]ATTTTTAGCAAGTTT | 55130 |
| rs529558434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27977293 | GACTCGGCCGGGCAC[A/G]GTGGCTCACACCTGT | 55130 |
| rs529587170 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27832675 | ATTACCAGAGCACAC[G/T]TGACCAGGAATGCTA | 55130 |
| rs529609727 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27960601 | ACGATCCACCCTCCT[A/C/T]GGCCTCCCAAAGTGC | 55130 |
| rs529666810 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27848829 | CTGGCCATCAGAGAA[A/T]TGCAAATCAAAACCA | 55130 |
| rs529710962 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27929955 | TTTTCTTCTGTTATA[A/T]CTTTACTTAAGATCA | 55130 |
| rs529732782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27866607 | ACAAGAAACATGGTG[C/T]CAGCATCTGCTTCTG | 55130 |
| rs529735309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27903205 | GACAAAAACCACATG[A/G]TTATCTCAATAGATG | 55130 |
| rs529737431 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27994683 | CCTGTTAAAAGAAAT[G/T]TACCCACAAAAATTA | 55130 |
| rs529739208 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983424 | CTTCATAGGGCACTG[A/T]CTCCTACCTTCTACA | 55130 |
| rs529783997 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27942940 | TTGGAAAATTTCTGA[A/C]CACATTTTTCAGTGT | 55130 |
| rs529785849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27935751 | TATTAACCACTAATA[C/T]ATTTTACCATCTCTC | 55130 |
| rs529795005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27890380 | TAATAGATGAAGTTA[C/T]TAATTTAATAAGTAA | 55130 |
| rs529796057 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27865416 | CAAACCTTTTCTGTC[G/T]GTCTTCCTGTTAGCT | 55130 |
| rs529852468 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27949428 | TAACTTGGAGCATCA[C/T]TCACAGGGAAAGAAC | 55130 |
| rs529864791 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27948359 | TATAAATCTTTCAGA[A/G]TGAATACCAGAGGAC | 55130 |
| rs529877031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27815016 | CTTCAATCTTCAGTT[C/T]TTCTTTTTAGCCCCC | 55130 |
| rs529907685 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27914219 | GCATTGAAACACATC[A/G]AGAGGCACAAAATAT | 55130 |
| rs529920060 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27862840 | CATATGTAGCACATA[C/T]AAAAATTCAGTTTCA | 55130 |
| rs529937139 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27861715 | ATCCTTCTTTGTATA[C/G]GTAATTGCCCTGTAA | 55130 |
| rs529939727 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27954883 | CCAGTAATCCAAATA[C/T]TTAAAGTGGATTCAC | 55130 |
| rs529943114 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27837969 | TGACATCTTACCCCA[C/T]GGCGATGGATTGGGA | 55130 |
| rs529946678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27902694 | AATAAACTAGAAAAT[C/T]GAGAAGAAATGGATA | 55130 |
| rs529956118 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | ARMC4 | GRCh38.p7 | 10:27820835 | TTGCCCAGGCTAGAG[G/T]GTAATGGTGTGATCT | 55130 |
| rs529962686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27990180 | AGAGACAAGATCTTG[C/T]TCTGTCACCCAGGCT | 55130 |
| rs529974072 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27868766 | TTAATAGGTGCAGCA[A/C/G]ACCACCATGGCACAC | 55130 |
| rs529975981 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27861119 | GCCTCAGCCTCCCAA[A/G]TAGCTGAGATTACAG | 55130 |
| rs530007352 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27908115 | TAGTAACATTTAAAT[A/G]CTTTCCAAAACAAAT | 55130 |
| rs530034106 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27955191 | TTCCGTTTTCGAAAT[A/T]CTCTTTTTAACAAGA | 55130 |
| rs530058866 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27828659 | TTAAAGCAATAAAAG[A/T]TATGCACCATTTATT | 55130 |
| rs530070438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27968901 | GGCTTTAGGGAACTC[A/G]TCTTGCTGACCAGAA | 55130 |
| rs530109026 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27943878 | AAGCTTTTGACGTTT[C/T]AAAGTTTTCAGCATT | 55130 |
| rs530171246 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27907254 | CAAAGCAACACAGAA[C/T]GTAGTGCTCTCTCAC | 55130 |
| rs530180077 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27880763 | TGATCTTGGACTTCC[A/C]AGCCTCCAGAATTGT | 55130 |
| rs530187850 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27974692 | CGGTCTGTTTTTGTT[G/T]TTTTTTTTTTTGCTT | 55130 |
| rs530196783 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27921903 | CGGGCGCCTTGGCTC[A/G]TGCCTGTAATCCCAG | 55130 |
| rs530203316 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27834676 | GGGAAGCCATGCTAG[C/T]GTTTTCAAAAGAGCA | 55130 |
| rs530215435 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27934254 | GTCTTTATCAGCAGC[A/C]TGAAAATGGACTAAT | 55130 |
| rs530233072 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27967681 | AGATCACTTGAGGTC[A/T]GGAGTTCAAGACCAG | 55130 |
| rs530245963 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27841709 | AGATCTGCTTCCAGT[C/G]TTTCTGATCCTGTCC | 55130 |
| rs530275193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27896632 | TCCTTTTGCTTGGTG[C/T]TCTAGAAATCTTTTA | 55130 |
| rs530310289 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27896093 | TCCCAATGCACTTTT[C/G]AAAAGCTGTGTATCT | 55130 |
| rs530316119 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27988909 | TCTGGGTATTTGGAG[A/G]AAGCCAAACATAATC | 55130 |
| rs530327693 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | ARMC4 | GRCh38.p7 | 10:27847309 | AGCATATAAACAGAA[C/T]CAAAGACAAAAACCA | 55130 |
| rs530328929 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27989402 | ATGACATGCATTGTT[C/T]ACAAAATGTATATTT | 55130 |
| rs530354058 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27897049 | TTCACTTTTCAAGGG[A/T]AATTGTCTTCTTAGG | 55130 |
| rs530357591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27982374 | GATATCTCCATGCTA[A/G]ATAAGTTATATGTAT | 55130 |
| rs530378194 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27827719 | TCATCTTCCAGCCCC[A/G]TTCCCATCCATTCTC | 55130 |
| rs530391768 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27970552 | TCTCTTCCCTTCACA[A/G]TGCTCCACACATAAA | 55130 |
| rs530397752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27836712 | TAATTTCTTTAGGAT[C/T]TCAAGGAATACGAAA | 55130 |
| rs530426690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27844237 | AATTAAGAATATATA[C/T]CAGCTGCAAGAGCAG | 55130 |
| rs530431839 | in-del | -/GT | 0.00279329 | 0.0372672 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940323 | AATGTCAGCATATAC[-/GT]GTGAGATTTATATAA | 55130 |
| rs530456908 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27886370 | GACAGTGAGATTACA[G/T]ATTTAAAATGATAAT | 55130 |
| rs530464372 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940919 | TCAAAAACAAGAATG[C/T]TTTAAAAAATCACTT | 55130 |
| rs530477528 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27937039 | TCATCTTTCTACTAG[C/T]AGCTTTCTGACAGCA | 55130 |
| rs530486715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27970139 | ATAAATAAATAAATA[A/G]ATAAATAAATCTCTA | 55130 |
| rs530507298 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27877702 | TTCCACCTTCTCACA[C/T]GTCTTAAAAACCTAG | 55130 |
| rs530507951 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27907977 | CAGTTTTAAATCCAT[C/G]ACACAGAAAACAAGC | 55130 |
| rs530508014 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27898848 | TCTTTTTAATTTTTT[G/T]GCTGTGATAACAAAT | 55130 |
| rs530523324 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27889545 | TGTCTCTTAGTCTTA[A/T]GATCTCATGGGTCTC | 55130 |
| rs530536443 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27932748 | AAGTAACCAACTCCC[A/C]CCCAGTCACTCTTTC | 55130 |
| rs530557173 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27923316 | GATCAAGATATATCA[A/C]GCAAATGGAAACAGT | 55130 |
| rs530565439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27935657 | ATTGTACCTATTTGG[A/G]TTTAATAGGTCTCTT | 55130 |
| rs530585714 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27852677 | CATTTAAAGCTAACC[A/G]TGGCCGGGCACAGTG | 55130 |
| rs530597415 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27882687 | CCAGCTCCACAGTAG[C/G]CTTGAAGATCAGCAA | 55130 |
| rs530605894 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27976847 | CAACTTCAAGACTTA[C/T]CATAAAGCTAGAGTA | 55130 |
| rs530642931 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27891369 | GTTTTCAAATTACTA[C/G]AGTTTTTTGTTTTTT | 55130 |
| rs530661127 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27991652 | CGGCAGAATTTCAGC[A/G]TAGATAAAACTTAAC | 55130 |
| rs530670090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27843733 | GATCACACCATTGCA[C/T]TCCTGCCTGGGTGAC | 55130 |
| rs530678234 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27905846 | TGGACCTCTTCCTTA[A/C]ACCTTATACAAAAAT | 55130 |
| rs530688519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27908809 | GGAGATCAGTTTTGC[A/G]TAACTTTATAAAATT | 55130 |
| rs530708381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27848894 | GATCATTAAAAAGTC[A/G]GGAAACAACACGTGC | 55130 |
| rs530727985 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27990812 | CATTGCTCTGGTGAC[C/T]TGACTTCCTGTCCCA | 55130 |
| rs530728793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27822225 | AATTTTTACATTTCC[A/G]TTTAACAGTTTATGA | 55130 |
| rs530736835 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27978068 | CAAAAATGTTCTTAG[A/T]AGTTTTATTTGTAAT | 55130 |
| rs530757875 | in-del | -/A | 0.0162398 | 0.0886349 | intron-variant | ARMC4 | GRCh38.p7 | 10:27926005 | AGTGAGACTCCAGCT[-/A]AAAAAAAAAAAAAAA | 55130 |
| rs530818534 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27981926 | GCATTATGACCTCAC[A/G]AGCCTTAGTTGATGA | 55130 |
| rs530841530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27991057 | AAGAATCAAAGTGCC[C/T]TGGTTCTATGTACCA | 55130 |
| rs530844320 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27914740 | TACACATACTTTATA[A/T]ATGTATATAAAATGG | 55130 |
| rs530884109 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27874821 | CTTTGGTGAATCTGA[A/C]AATTATGTGTCTTGG | 55130 |
| rs530900388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27955285 | GTCTAATATGGCCTT[C/T]CAAACATGAATACTG | 55130 |
| rs530900474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27962452 | CAAGGCCCTAAAGTG[A/G]AAGAGTCTCTTTTAC | 55130 |
| rs530952310 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872334 | CCTCTTTTCCTAATT[A/G]AATACCCTTTATTTC | 55130 |
| rs530960279 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27868954 | AGAAAGACATGCCTA[A/C]AAAACAGATGAAAAC | 55130 |
| rs530973984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27967741 | ACTAAAAATAAAAAA[A/G]TTAGCTGAGTGTGGT | 55130 |
| rs530986350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27842533 | ACTATTTTTCACAAA[C/T]AGTTATCAATCTTCT | 55130 |
| rs530998923 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27874957 | CAGAGTGTTTTCCAA[C/G]TTGGTTCCATTCTCC | 55130 |
| rs531033796 | snp | C/G | 0.00268546 | 0.0365447 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27968933 | CATACCGAAGTAATT[C/G]TGCTCTTCCGTGTGA | 55130 |
| rs531047529 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27880897 | CAGAATGTATTCATT[C/G]GTGGGTGGGAATGGA | 55130 |
| rs531049442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27890225 | TTAAGCAAGTGAACT[A/G]GAAGAAGAGGCCATC | 55130 |
| rs531057507 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27937286 | GTCAGCTCTTCAATG[A/G]CCCCTGAAATCTAGA | 55130 |
| rs531060983 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27828832 | ATTGTTTAATATAAG[A/C]AAAAAGCCAAACTGA | 55130 |
| rs531062846 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27835384 | CATCTCACACCTGTA[G/T]CCTGAACTTGACAAT | 55130 |
| rs531062950 | snp | A/G | 0.000234655 | 0.0108292 | synonymous-codon, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27961688 | GGAGCTATCGCTAAC[A/G]GTTTCCTCAATCTTT | 55130 |
| rs531084048 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27912735 | TTGCTTAAAAGAACA[C/T]GACGTTCTTAAACCA | 55130 |
| rs531090870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27975538 | CAACTTACACCAAAT[A/G]AACAAATTCCTTTAA | 55130 |
| rs531092262 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27982447 | CCCCCTCCAGAAGGT[A/C]AAAGAAAATCATTCC | 55130 |
| rs531101590 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27834855 | CACACCTAAGTCATA[C/G]AGTCTCCAAAGAAAT | 55130 |
| rs531129993 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27974804 | AATTTGATAGGAATA[G/T]CATTGAATCTATAAA | 55130 |
| rs531159057 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27896195 | ATTATACACGTCAAT[G/T]AAATTTTGTCCCTGC | 55130 |
| rs531159218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27929011 | AATGGTTCCAGAATC[C/T]ATATGTTTAGCCATT | 55130 |
| rs531183792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27854089 | ATGTGAACACTTTGC[C/T]CGAGGAGTTATACAG | 55130 |
| rs531184537 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27847428 | GGGACGTATCTCAAA[A/C]TAATAAGAGCTATTT | 55130 |
| rs531221842 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27853484 | AAAAGCTATAAAACT[G/T]TAGTATGCTAATATT | 55130 |
| rs531250333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27896714 | CTGTCTTTTTTTCTC[C/T]ATCTGTGCTTGTGTA | 55130 |
| rs531253231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27989583 | TACCAAGCTACTTAA[C/T]TAGAGAGAGTGAAAC | 55130 |
| rs531267069 | in-del | -/TATT | 0.0134861 | 0.0810011 | intron-variant | ARMC4 | GRCh38.p7 | 10:27885836 | ATATATAAATATATA[-/TATT]TGTTTGGATATATAT | 55130 |
| rs531274735 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27847879 | GGGATGTGAAGGTAC[A/T]CTTCAAGGAGAACTA | 55130 |
| rs531280201 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27927573 | AAAACACACGTGGGA[C/T]GCCTATGTTCACAGG | 55130 |
| rs531291933 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27861873 | CCAAGCATCCTTCCA[C/G]GGTTTGAATTTCTGC | 55130 |
| rs531319315 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27947858 | CTAACATTCTTAATC[A/G]CTCGTGCTGAGGACT | 55130 |
| rs531332900 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27878646 | ACATCACATACAAAC[-/T]TTTTTTAATCCTACA | 55130 |
| rs531355503 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27941606 | ATCCAGTTTTTTTTT[G/T]TTTTTTTTTTGCAAT | 55130 |
| rs531356120 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27859781 | GTTGGTTTGCAATGT[A/G]TAGGTAAGTTAGAGT | 55130 |
| rs531376252 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27814172 | AAGGGAAACAGGGAC[C/G]CTCCGCAAAGCCAGA | 55130 |
| rs531384720 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27902030 | ACCACATCACACTTA[A/T]TCTAAAATTGACCAC | 55130 |
| rs531410446 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27941963 | GGCTTGAGACAGGTG[A/G]ACACTCCTGGTCTAA | 55130 |
| rs531412663 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27933457 | CATTATCAGATATGC[A/C]GTTTAGGAAAGTAAA | 55130 |
| rs531413111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27813720 | TTACTCTATAGGTAA[C/T]AAAAAGAAGTTATTT | 55130 |
| rs531426925 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27867343 | AATGCCACAAAGTCT[A/G]ATGGTGCTGGGGTGT | 55130 |
| rs531443051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27996552 | TGCTGTAACCTCCAG[A/G]CATCTAGTAAGTGAA | 55130 |
| rs531443607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27907259 | CAACACAGAACGTAG[C/T]GCTCTCTCACTGCAG | 55130 |
| rs531474706 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872756 | TGCTGGATTCAGTTT[A/G]CCAGTATTTTATTGA | 55130 |
| rs531487224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27827509 | TTTCTTCTCTCCTCC[C/T]TAAATCCTGCTGTCC | 55130 |
| rs531491442 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27833966 | GAAAGGACAGCGGTG[A/G]AGGTTCCACATGGCG | 55130 |
| rs531496965 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27826697 | ATCCTCCTGCCTCCC[A/T]CTCCACATCCTCTGG | 55130 |
| rs531537381 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27912813 | GGCAATTCAGTAAAA[C/T]GGGAAACATAAATGT | 55130 |
| rs531553468 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27914974 | AAACAACATATGCAT[A/G]ATTGGAATACCAAGA | 55130 |
| rs531565559 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27873191 | GTATTTTTGTGGGAT[C/T]GGTGGTGATATCCCC | 55130 |
| rs531580187 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27933375 | GAATAGCAAGTTAAG[C/T]ACCTTAGTATTAAAA | 55130 |
| rs531592951 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27927024 | TTTAGATCTGGTGGT[G/T]GGGCATAAGGCATAA | 55130 |
| rs531600976 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27880446 | ACTTTATATTGGAAT[C/T]ACCTGGAGAGTTTTT | 55130 |
| rs531603689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27879674 | CAATTTATGAAGAGA[C/T]TGTTTTCCAAAAGTT | 55130 |
| rs531622640 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27889704 | AAGTCTCCCAGCCCT[A/G]TGTACTCAATGATGT | 55130 |
| rs531629938 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27926088 | AAGAGCTAGATATTA[G/T]TTTAGTCTTTAGTCT | 55130 |
| rs531632852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27973896 | CTAATTTACACCCAC[C/T]AACAGTGTGTACGTA | 55130 |
| rs531644123 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27828272 | ACTTCCCTGATATGA[C/T]GATTTCCCCAGTGGG | 55130 |
| rs531720708 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27964544 | CTATTGAAGAATGCT[G/T]TCTTTCGGTATCTTT | 55130 |
| rs531731373 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27846870 | CCTCCCAAGACTAAA[A/C]CAGGAAGAAGTTGAA | 55130 |
| rs531751078 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27851732 | CGTTTACAAGGACAG[C/T]AAAAAGAGAACAGGA | 55130 |
| rs531773419 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27868625 | TCATAAGTGGGAGCT[A/G]AACAATGAGAACACA | 55130 |
| rs531787668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27851535 | GAAACGTCGATAGTA[C/T]TGCAGATGTAAAACA | 55130 |
| rs531798595 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27939622 | AAACACCTGAAGTGC[C/T]GGCTACTTGGGAGGC | 55130 |
| rs531809496 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27895401 | TGGGTTCAAATGATT[A/C]TTGTGCCTCCCAAGT | 55130 |
| rs531816632 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27886997 | CAGAAAACAAAGCAC[A/C]AAACAGCAAAAATAA | 55130 |
| rs531820860 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27979735 | CAAATAAATGGAAAG[A/C]TATCTCCTGTTCATA | 55130 |
| rs531822757 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27988360 | TTTTTTTTTTTGAGA[C/G]AGAGTATCCCTCTGT | 55130 |
| rs531840796 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997188 | TATTCTAGCATTTTG[C/T]TTCTATTGCTAACCG | 55130 |
| rs531857585 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27900467 | AAGAATGAGTTTGAC[A/G]AATTGACAGAAGTAG | 55130 |
| rs531857944 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27894943 | AATGAATTATGATAT[A/T]TCCATACAATATAAT | 55130 |
| rs531858671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27911268 | ACGAAAAGTCAGAAT[A/G]TCACCTTTTTGGACC | 55130 |
| rs531860570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27818680 | GAGAATAGATTGCTA[A/G]CTACAGCAACTCCAC | 55130 |
| rs531864997 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:28000380 | AAGGGGCTTATGCTA[A/G]TAGGTATACAGAGAA | 55130 |
| rs531866271 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27980404 | TTATAAGGCAACCTG[C/T]AGAACAAGAGAAAAA | 55130 |
| rs531871739 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27852638 | AGCAGATGGGAAAAA[C/T]AGAAAACAAATAACA | 55130 |
| rs531890276 | in-del | -/G | 0.00557542 | 0.0525036 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999711 | GCACTATCTTGGGGT[-/G]GGGGGACACGGTGTT | 55130 |
| rs531892760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27905569 | GCCAAGACAATCTTA[A/G]GCAAAAAGAACAAGG | 55130 |
| rs531962974 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27848373 | TGGCTAGCCATATGT[A/C]GGAAGCTGAAACTGG | 55130 |
| rs531987159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27987615 | TTAAATTTAAGACAT[C/T]TAGACAGATTATTCC | 55130 |
| rs531995843 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, stop-gained | ARMC4 | GRCh38.p7 | 10:27858180 | CAAATATCAAATTAT[G/T]ATTCTACCAACACCC | 55130 |
| rs531997021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27854765 | TGTCACAAAACAAAA[C/T]TAAACAAAACAAAAA | 55130 |
| rs532005132 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27860498 | GCTTGAATGCAGCCA[C/T]GATGCAGCAGGCAGG | 55130 |
| rs532031052 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27897167 | ATCCCCTTCCCACCC[A/G]CCTGCCTTCTTTCTT | 55130 |
| rs532046989 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27956489 | TCCAACTGTGCTTGC[A/C]AATATAACCCTTGTT | 55130 |
| rs532085890 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27907902 | AATTTTTTTTTTTTT[G/T]GCAAAACTTCATCAA | 55130 |
| rs532091243 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27814856 | AACTGAGTCCTGCGG[A/G]AGGCATATGTCAACA | 55130 |
| rs532097630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27897334 | GATTCGTGTATTCAA[A/G]TGACTGGACATCTCT | 55130 |
| rs532105957 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27954611 | TGGTAGCATAGTGCT[A/G]GCTAGTGGTCGCATA | 55130 |
| rs532109274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27942135 | TGCTCAGAAAGCCCG[C/T]AGCATTTGTGACTGT | 55130 |
| rs532125632 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27948252 | GGCTTGAGGGATTTT[A/T]TTTTAGAACAGTTTT | 55130 |
| rs532125875 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27841596 | AGACGGGGTTTCACC[A/T]TGTTGGCCAGGCTGG | 55130 |
| rs532126143 | snp | A/C | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983634 | AGCCCATTTCTTATC[A/C]GATTGGCTTAATGAC | 55130 |
| rs532131832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27820744 | TGGTTGGTTAAATTT[C/T]AGCTTAACAATTAAA | 55130 |
| rs532176595 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27947871 | TCGCTCGTGCTGAGG[A/T]CTTGCTTGACTGCTA | 55130 |
| rs532224063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27902110 | TAACAAACAGTCTCT[C/T]GGACCACAGTGCAAT | 55130 |
| rs532239454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27990082 | GGGAGCTAAAAATTC[C/T]GTTTATACTCTAAAG | 55130 |
| rs532258809 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27902606 | CACAATAAAAAATGA[A/T]ACAGGGGAGATCACC | 55130 |
| rs532269705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27820214 | AGGCTCCACATGCCA[C/T]TGGCTGCTGCCACCC | 55130 |
| rs532298136 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27953983 | GAGAAAAATCTCAAA[A/G]GCCAATGGACCAAAA | 55130 |
| rs532354331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27966643 | TAAGAAATACTTCTC[C/T]ACCACAGAATTCTAT | 55130 |
| rs532358500 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27868299 | TCTAGAACCAGAAAT[A/G]AAATTTGACCTAGAA | 55130 |
| rs532374219 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27996582 | AAAACTTCAGATAAG[A/C]ACTACCTGAGCCTAG | 55130 |
| rs532406559 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27922135 | TTCCAACCTGGGTGA[C/T]AGAGTGAAACTCTGC | 55130 |
| rs532407788 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27874093 | CCTTGTTGAATTGAT[A/C]CCTTTACCATTATGT | 55130 |
| rs532424742 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27947022 | GCTGTCCTCCACATT[C/T]ATGATTAAGTTCAGA | 55130 |
| rs532427601 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27967552 | GCCTGGAGAAGCAAC[A/G]CATACCTCATCCTGC | 55130 |
| rs532447714 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27865800 | CTACTAAATGGTGAA[A/G]GCAGGACACGAGTCA | 55130 |
| rs532500096 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27978895 | GGCTCAATGGTGAAA[A/G]CCTAAAAGCTTTTCA | 55130 |
| rs532502824 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27974621 | GTACCATGTTGTTTC[C/G]GTTACTGTAGCCCTG | 55130 |
| rs532508468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27833980 | GAAGGTTCCACATGG[C/T]GCCACCTTACAGGGA | 55130 |
| rs532520311 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27901541 | ATAAAGATCAAGACC[C/T]ACCGGTGTGCTGTAT | 55130 |
| rs532542810 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27840300 | AAACAGCCTAAATAA[C/G]AGTGTGACAAAAGAT | 55130 |
| rs532549675 | snp | G/T | 0.0490535 | 0.14873 | intron-variant | ARMC4 | GRCh38.p7 | 10:27873519 | TTTCCCTCTACACAC[G/T]GCTTTAAATGTGTCC | 55130 |
| rs532572855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940209 | TATATATATATAGTG[C/T]ATAGATATATATGTC | 55130 |
| rs532612758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27888274 | ACTAATTTACATTCC[C/T]ACCAACAGTGTATAA | 55130 |
| rs532616694 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27898742 | AACATATTTGTGATA[G/T]GTATTGATATTGACG | 55130 |
| rs532630544 | snp | A/G | 0.000100179 | 0.00707667 | missense, utr-variant-5-prime, intron-variant | ARMC4 | GRCh38.p7 | 10:27981495 | TTTCTGAAAATTTTG[A/G]TGATTTTTCTCTTAA | 55130 |
| rs532632422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27973457 | AAGCCTAGTATCCAA[C/T]AGTTATTTTTTCTGA | 55130 |
| rs532643490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27895528 | CCCTGGCTTCCAGCT[A/G]TTCACCCGCCTCGGC | 55130 |
| rs532650423 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27896040 | TCTCTCATTTCAAGC[A/G]TTCACTAGACAAGTG | 55130 |
| rs532670428 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27974054 | TTGAGCTTTTTTCAC[A/T]TGCTTGTTGGCCACA | 55130 |
| rs532680327 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | ARMC4 | GRCh38.p7 | 10:27923992 | AGAAAGAAAGAAAGA[A/G]AGAAAGAAAGAAAGA | 55130 |
| rs532694960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27847273 | GCTTGTTCAACATAC[A/G]CAAATCAATAAACGT | 55130 |
| rs532697718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27988407 | CAGTGGCGTGATCTC[A/G]GGTCACTGCAACCTC | 55130 |
| rs532731258 | snp | A/G | 0.0167003 | 0.0898401 | intron-variant, stop-gained | ARMC4 | GRCh38.p7 | 10:27853282 | TGAGGCAGGAGAATC[A/G]CTTGAATCCGGGAGG | 55130 |
| rs532739259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27946918 | GAAAATTTCTTCCAT[A/G]CCTCTAGAAATGTCC | 55130 |
| rs532755252 | snp | A/G | 3.29832e-05 | 0.00406085 | missense | ARMC4 | GRCh38.p7 | 10:27940759 | GCCTCATACAGACTC[A/G]ATTGGGCAGGTTTTG | 55130 |
| rs532766677 | in-del | -/TG | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27910649 | CTAATCTCAGCTACT[-/TG]GGAGGCTGAGGTAGG | 55130 |
| rs532784803 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27988744 | CTTATTACTGACGAT[A/C]TCACTAGAATAAAAA | 55130 |
| rs532793300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27859404 | AACATCATATTCTTC[C/T]ACTGGAATAGATTTC | 55130 |
| rs532798471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27980535 | AGACATTTCTTCAAA[A/G]AAGATATACAGATAA | 55130 |
| rs532804210 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27905654 | AAACAGCATGGTACT[C/G]GTACCAAAACAGATA | 55130 |
| rs532817596 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27866490 | TCAACTTTTCCAAGG[A/T]TCATCTTGGTCCAAT | 55130 |
| rs532850455 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27918429 | ATCACCTTATTTATT[A/T]ATAGAACAAAAGAAA | 55130 |
| rs532863685 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27819258 | TGGGACAGAAAAGAG[A/C]AACAGAAATAGAAGG | 55130 |
| rs532864433 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27884852 | ACATACAGGCTCAGG[C/T]AGGATGAATGCTCAG | 55130 |
| rs532887092 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27945609 | ATCGCTACATGTAAA[A/G]AGTAGTAGTGAGATG | 55130 |
| rs532887188 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27975109 | TTTGTATCCTGAAAC[A/G]TTGCTGAAGTTGTTT | 55130 |
| rs532887883 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27911421 | ATGAATTCATCAATT[C/G]AGAATTTGCAAATAA | 55130 |
| rs532898489 | in-del | -/G | 0.00557542 | 0.0525036 | intron-variant | ARMC4 | GRCh38.p7 | 10:27864742 | TCTCTAAGGTTGTAT[-/G]GGGGTGAGTGTAATG | 55130 |
| rs532922917 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27911683 | CTTAAGGTCTACAAC[A/G]AAACCTCTTTCGCAA | 55130 |
| rs532931249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27952461 | TGTTACATAGGTAAA[C/T]GTGTGCCATGTGGTT | 55130 |
| rs532948281 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27908336 | GCAAGACTAACATTG[A/C]AGACTGTGTTATAAT | 55130 |
| rs532968472 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27953097 | TGTGCAATCATTACT[A/G]CGATGAAAGTAATAA | 55130 |
| rs532971960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27994908 | ATCCTAGAAGCAAGT[A/G]ACTGGCTTACCTGAC | 55130 |
| rs532991333 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ARMC4 | GRCh38.p7 | 10:27838101 | AGGGAATATTAATGC[A/G]AGCATATTTTTGGCA | 55130 |
| rs533036656 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27978874 | AAAATCCCACAGCTA[A/C]CATCAGGCTCAATGG | 55130 |
| rs533042624 | in-del | -/G | 0.00676609 | 0.0577691 | intron-variant | ARMC4 | GRCh38.p7 | 10:27942447 | ATCAGTTAGTCTATA[-/G]GAAAACTGGTTTTGT | 55130 |
| rs533047662 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27919075 | GCAATATATACCTCA[C/T]TAATGGATTGGCAGT | 55130 |
| rs533051267 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27911650 | AGCCATCTCCGTATT[C/T]TACATAGTAATCCAT | 55130 |
| rs533088804 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27893871 | ACCTTATTAGAAGGC[A/C]AGGTGTGGTGACTCA | 55130 |
| rs533096074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27832514 | ACTTTCCCCCCACCC[A/G]TGTTGTTCACACACA | 55130 |
| rs533117024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27845394 | TTTGTCACCACCAGG[C/T]CTGCCCTAAAAGAGC | 55130 |
| rs533122216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27838706 | ATTGAATTTGGCAAA[A/G]GTACCCAGTAGCAAT | 55130 |
| rs533135992 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27850543 | GACTGGGTGACAGAG[C/T]GAGACTCTGTCCCAA | 55130 |
| rs533148399 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27924842 | AAAAACATAAATAGA[A/C]CACTTTACATAGAAG | 55130 |
| rs533152079 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27852020 | GATAATAAAATGGAG[C/G]ACCATGTTTAAAGTT | 55130 |
| rs533152127 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27814213 | GTGCACTTCCTGACT[C/T]GCAGATTGAATCCCA | 55130 |
| rs533154048 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27845910 | CAATACAGGAGCACC[C/T]AGATTCATAAAGCAA | 55130 |
| rs533171697 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27850177 | TTGCTGGGCGTGGCG[G/T]CTCACACCTGTAATC | 55130 |
| rs533186517 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27938647 | CTCACTGTCTCAGGC[C/T]GAAGTCCAGTGGCGC | 55130 |
| rs533191804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27886742 | TGTGGCATTCATAAC[A/G]TAGTGTGTGGGTGGA | 55130 |
| rs533212662 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27818489 | TTATTACTTTATGAA[C/T]TTTGTTATTACAGCC | 55130 |
| rs533212807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27931960 | AATATACCTAACCTA[C/T]TGAACATCATAGCTT | 55130 |
| rs533213094 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27986906 | TATGGCTGAGAAAAG[G/T]GGAAAGGGAGACTAT | 55130 |
| rs533226074 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27936024 | TTAAGATAAAAGTTC[C/T]ATTAGCCGAGGTTAC | 55130 |
| rs533231294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27894766 | TAGAGGAGTCTCCCT[A/G]TGCTCCCCCAGCTGA | 55130 |
| rs533255120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27985965 | CTTGTTTAGAATGGA[A/G]AAATTTGAGAAAGAT | 55130 |
| rs533288456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27817519 | TTTCCCATCTTTTGG[A/G]GTCTCCAATGTCTAT | 55130 |
| rs533291451 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27933354 | GGCCATAAGACAAAA[A/T]GCTTTGAATAGCAAG | 55130 |
| rs533303017 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27964267 | CCATGGTTAGTGAAG[C/T]GGCTGTGCTAAAACA | 55130 |
| rs533315774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27899713 | GAAGTTCGAACTGGG[C/T]GGAGCCCACCACAGC | 55130 |
| rs533315888 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27849287 | AACCATCATTCTCAG[C/T]AAACTAACACAGGAA | 55130 |
| rs533317740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27817824 | TATGTTTTTGACACC[A/G]TGATTTCTTTCCCTT | 55130 |
| rs533321186 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27957479 | AGTAAGACAGACAAC[A/C]TGAACCATCAGGATA | 55130 |
| rs533324602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27823900 | AATCCCAGCACTTTG[A/G]GAGGCCGAGGCGGGC | 55130 |
| rs533359277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27950997 | AAATGTTTAACTTGA[A/G]AAAAGTTCCCATGTC | 55130 |
| rs533369575 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27845793 | TCTGATAAAACAGAC[-/T]TTTAAACCAACAAAT | 55130 |
| rs533418845 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27993266 | AGATCATATTTCAAA[C/G]CTTAGGAAAAAAGCT | 55130 |
| rs533433768 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999633 | CCAGCAAGAGCCCCA[A/G]CTGGAACACCAGTGA | 55130 |
| rs533459058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27916211 | CAGGAGATCAAAAGC[C/T]GAGCAGGGTGAGGAG | 55130 |
| rs533480013 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27830973 | GTCCTTTTTCCTTTG[C/T]TCTATCAGGTAGAGA | 55130 |
| rs533481939 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27837239 | ACTGGTCACTCAGAG[G/T]GAGACCTATCGTGGG | 55130 |
| rs533493045 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ARMC4 | GRCh38.p7 | 10:27963807 | TTGAAGTGAGTTTTT[C/T]AGACCCCCATGCATT | 55130 |
| rs533559222 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27932975 | AGGAATAAATAAGGA[G/T]CTGGGTGTGGTGGCT | 55130 |
| rs533596065 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999093 | CTGGGTTCCACCCGC[C/G]CCGGCCACCTGCTGC | 55130 |
| rs533603457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27863476 | GCATGTCCAAGAATG[A/G]CCATATTGAGTAGGG | 55130 |
| rs533612820 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27900148 | TTGCTGTTCTGCAGC[C/G]TCCGCTCATGATACC | 55130 |
| rs533641121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27915608 | GGGGAATTATGATAC[A/G]ATTAAATTCTGACTT | 55130 |
| rs533641290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27870402 | GGTACATGTGCTCAA[C/T]ATGCAGGTTTGTTAC | 55130 |
| rs533648596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27900605 | TAGAATAATCACTTT[A/G]GAGAAGAACAGAAAT | 55130 |
| rs533651734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27875147 | TCCAGTTGATTGAAT[C/T]GGCTACTAAAGCTTG | 55130 |
| rs533663222 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27987764 | CCAATAGGATATAAC[C/G]AAGGAAGAATTTTTT | 55130 |
| rs533665204 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | ARMC4 | GRCh38.p7 | 10:27811898 | CTTGTGATTTGCATG[A/G]TCTGGTACAGTGACA | 55130 |
| rs533668181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27909375 | CTTTAAAACAAGTTA[C/T]AGACAAAATTTCACA | 55130 |
| rs533670454 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ARMC4 | GRCh38.p7 | 10:27876008 | GGGGGAGGGGCACCC[A/G]CCATTGCTGAGGCTT | 55130 |
| rs533674152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27963254 | CCTCGTGATCCTCCC[A/G]TCTCGGCCTCCCAAA | 55130 |
| rs533737284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27866603 | CTTTACAAGAAACAT[A/G]GTGCCAGCATCTGCT | 55130 |
| rs533737830 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27922129 | ACTGCATTCCAACCT[C/G]GGTGACAGAGTGAAA | 55130 |
| rs533742848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27911005 | ATAGATTGTTGAATC[A/G]TGAATATTGGACTTA | 55130 |
| rs533745281 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27858383 | TAAGGTCTGCCTCTA[C/T]GTTATTGCAGAGTAA | 55130 |
| rs533750864 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27857370 | GATGTTTTTGGTCAA[C/T]AGTAGGCTATTAGTA | 55130 |
| rs533773658 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27865275 | ATGTGATTCATTAAG[G/T]CTGGGTGAGGTCCAC | 55130 |
| rs533775966 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27865737 | TTTGCAAACTCATAG[C/T]CTTAAAAGAAAGCTT | 55130 |
| rs533778251 | snp | C/T | 0.00119904 | 0.0244557 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940322 | AAATGTCAGCATATA[C/T]GTGTGAGATTTATAT | 55130 |
| rs533780805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27905067 | GGCTTGAGCGCTGAG[C/T]CCAGCTGCAGATCTA | 55130 |
| rs533806656 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27851775 | TGAAGAAATAATGGC[A/T]GAAAAATTTCTAAAT | 55130 |
| rs533844664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27871097 | GATTTGTACTTCTCT[A/G]ATGGCCACTGATGAT | 55130 |
| rs533845657 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27917204 | GACCTTGTGGTTTTA[A/C]ACTAGAAATCAATAA | 55130 |
| rs533847323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27859025 | GCTATATGTCAGACA[C/T]TTTTACCTGGCTACT | 55130 |
| rs533891218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27818782 | GTCATTGTTGCTTTT[C/T]AAATCTGGAAAGAAG | 55130 |
| rs533907538 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27945691 | GATCAGTAAACCAGA[A/C]CTGCCAGGAGATTAA | 55130 |
| rs533908527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27831631 | GCCCTAGATTCCATG[C/T]TCTTATCTGCCATAC | 55130 |
| rs533911027 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27823176 | GGTGTCATTTGGAAT[-/G]GCCTCAAGTTGCTCT | 55130 |
| rs533923854 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27909129 | TTAAAATATAACTAA[C/T]GCCAATCTCTGAGCC | 55130 |
| rs533930506 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27818304 | ATTGTATAACCCCTC[A/G]ATTATAGGATTTTAA | 55130 |
| rs533944409 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27958723 | ACTTTGTGCTAAGCA[C/T]TTTACATGTGTTGTA | 55130 |
| rs533945151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27837678 | ACGTGGGTCATAAAG[A/G]ACGACAAAATAAACT | 55130 |
| rs533973352 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27963964 | TGGTGGCTCACGCCT[A/G]TAATCCCAGCACTTT | 55130 |
| rs533973357 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27971826 | CTTTACTAAGAATAA[A/G]ACAAAAATCTTTCAA | 55130 |
| rs534001751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27978501 | GGTGCACCAAGAAAA[A/G]GAAAACTGGAGCCGG | 55130 |
| rs534024117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27911474 | GGACCATTGGGAAAC[C/T]ACAGTCTTGTGAGGG | 55130 |
| rs534033103 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:28000505 | CCTTCGGAAGGATCC[C/T]GGAGTAGTCCCAGTC | 55130 |
| rs534054728 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27913256 | ATGGTACCTGATAGG[C/T]AGTTTTTCGATCCTC | 55130 |
| rs534059255 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27832979 | AAAGCATCAGTGCAA[C/T]ATGGCTTTTCCAACT | 55130 |
| rs534074052 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27842662 | AAAGTAGAAGCCAAA[A/T]ATAATTCCCCACAGT | 55130 |
| rs534082205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27931703 | TGAGAATTTAAAGAC[C/T]CATTTCAAAAAGTAA | 55130 |
| rs534110721 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27850218 | GGGAGGCCAAGACGG[C/G/T]TGAATCACTTGAGGT | 55130 |
| rs534112058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27824473 | CCCTTCTGCCATGGA[A/G]TGACCCTTGACAGAT | 55130 |
| rs534124199 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27830955 | AGTTTGGCAGGTGGA[C/T]AGGTCCTTTTTCCTT | 55130 |
| rs534140403 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27937881 | TACAAATATATACAA[G/T]TCAGGGCTATATACG | 55130 |
| rs534147118 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27849709 | AATTCCTACTGAAGA[C/T]AATCTGATTTTGCAA | 55130 |
| rs534156698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27986108 | TGTGGTCATGGGATA[C/T]GCCAAGGCCTTAAGG | 55130 |
| rs534162220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27838211 | CAAGATATTTTCTGA[A/G]TGCCAAAAACTACTT | 55130 |
| rs534202965 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27819769 | TTGACTATGGTTTGA[C/T]AGTGATTTTTCTAGG | 55130 |
| rs534203493 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27916881 | GTCTCTAACCCCTGT[C/G]TTGTTCAAGGGACAG | 55130 |
| rs534207730 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27924900 | TTAAAAAACTGTAGG[A/T]CCATATAATTGCATA | 55130 |
| rs534207830 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27948624 | TTTTAGGAGCTGGAG[-/A]AAAATAGAGTAAAAT | 55130 |
| rs534212609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27950247 | ACCTGGTGCCCAGCA[C/T]AAAGATTGGCTTAGA | 55130 |
| rs534244124 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | ARMC4 | GRCh38.p7 | 10:27885879 | TAAAAATATATATTT[A/G]TTTGGATATATATAT | 55130 |
| rs534254595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27943968 | CCTAACAACGTACAA[C/T]AGGTGGTGACAGTTA | 55130 |
| rs534263374 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27825242 | CACTGGTCTGAGCCA[C/G]TACTATCTCTTGAAC | 55130 |
| rs534289770 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27858338 | GAGACAATCTCCAGG[C/T]TGCATATTTCTGCTG | 55130 |
| rs534303971 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27978964 | GCTGTAATCCCAGCA[C/G]TTTGGGAGGCCGAGG | 55130 |
| rs534306878 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27893279 | TCTTAACACATACAT[C/G]TGAAAATGTGTTCTA | 55130 |
| rs534313931 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27915931 | AATTAGCAGGTGAGC[A/C]AACAAGGTTGTTTTA | 55130 |
| rs534323007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27863555 | TGAATAATGTGGATC[A/G]ACTTTATATATTCTT | 55130 |
| rs534345703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27892805 | TGATTCTGCTACTTC[A/G]TTGCCTGGCTCAATC | 55130 |
| rs534355010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27909514 | TTGATCTCATTACTG[A/G]TGTCTTAAAAGAAGA | 55130 |
| rs534374438 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27937284 | TGGTCAGCTCTTCAA[C/T]GGCCCCTGAAATCTA | 55130 |
| rs534376025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27923351 | AAGCAGGGATAAATA[C/T]TCTGTTACCAAACAA | 55130 |
| rs534437609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27899427 | GCAGGAGTGTTTTTT[C/T]CATACCCCAGTGGTG | 55130 |
| rs534457314 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27900951 | AACATTCAAATTCAG[A/G]AAATACAGAGAACAC | 55130 |
| rs534469214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27992166 | CTTCAAGGCACTCTT[A/G]GTTTTCATCAGCGCC | 55130 |
| rs534486700 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27991064 | AAAGTGCCTTGGTTC[C/T]ATGTACCACAGATGG | 55130 |
| rs534502856 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27899108 | TTTCCAATTGAGGTA[C/T]CCATCTCATCTCATT | 55130 |
| rs534503786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27930316 | TTGGAAGTTTGAGGC[A/G]GGAGGACTGCTTGAG | 55130 |
| rs534523480 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27915819 | TGTGGCAGAACAAAG[C/T]AGTCATCCATGATAT | 55130 |
| rs534547288 | in-del | -/A | 0.00795532 | 0.062565 | intron-variant | ARMC4 | GRCh38.p7 | 10:27992914 | TAAATGCATTTTTAT[-/A]AAAAAAATATTAATT | 55130 |
| rs534561769 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27882798 | CTCCATTCTAAAAAC[G/T]GCCTGTATGGCAATT | 55130 |
| rs534564699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27816248 | ATCTAGAGTAATTGC[C/T]TAAATTGTGAAATTC | 55130 |
| rs534599907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27998189 | GGTTGGTAACATCCA[C/T]GGGGAGTCCGCGCAT | 55130 |
| rs534641792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27998668 | GAAGGGGGCGGGTCT[C/T]GGTCCCCGGGAGGGA | 55130 |
| rs534657719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27936591 | TCTAAGAATCCCTTC[A/G]TTGGGCTAACTTCAT | 55130 |
| rs534697400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27962836 | GATGTCTCAGGAACT[A/G]CTCATCCATCACTCA | 55130 |
| rs534699708 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27873008 | ATTTTGGTTGGTAGG[A/C]TATTAATTGTTGCCT | 55130 |
| rs534728246 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27855049 | ATGTAAGGGTACCAG[A/G]AAACTGTGGGTGATC | 55130 |
| rs534731046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27956440 | CTCAGGAATAAGACC[A/G]CCTGGATGAAGCATT | 55130 |
| rs534738904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27897715 | ATGCATACAAGAGAG[A/G]GCAGTTCCTGGTGAG | 55130 |
| rs534798451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27897127 | TTTCTTGGCTTTTTT[A/G]TAATCAAGTTCTCCT | 55130 |
| rs534818902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27843763 | CAGAGCAATACTCTG[C/T]CTCAAAAAAAAACAA | 55130 |
| rs534820216 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27835662 | TGTATATTATATACT[A/G]TATTCTTAAAATAAG | 55130 |
| rs534856233 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27969724 | GGAGAAGGTCCCTGT[A/G]TGATCAACCAGGAAT | 55130 |
| rs534879680 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27976267 | TAAAAAGAAATAAAA[A/C]AACTGTTGAGATTGG | 55130 |
| rs534888158 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27869043 | CCTAAATTAGAATTG[C/T]TGAAGTTGTAATTAG | 55130 |
| rs534899589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27882088 | GTGGGAGGATCACTT[A/G]AGCCCAGGAGACAGA | 55130 |
| rs534917477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27977072 | GATCCATAACTCATA[C/T]ACACAAACCAAATTA | 55130 |
| rs534918526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27868566 | AGCCATCATCCTCAG[C/T]GAACTAACACACGAA | 55130 |
| rs534921198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27969287 | GTGTGAATCCTGCAC[C/T]CGATGCCTTCTACTC | 55130 |
| rs534933544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27913190 | TAAATAGGTAAATTA[C/T]GTGTCGCGGGGGTTT | 55130 |
| rs534934838 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27916167 | CTGAAAAGTGTGAAA[G/T]AAAGTGCCAATATAG | 55130 |
| rs534935086 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27914511 | AATTTGTTACTTGAC[A/T]TTATTCTATGAAAAA | 55130 |
| rs534936922 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27891020 | ATGGCTAAATCAGAG[C/T]TTGTGTTTATAGCAA | 55130 |
| rs534949649 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27994637 | AAGCAGCAATGGATG[C/T]TGGCAGTGTAGTGAC | 55130 |
| rs534955652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27874388 | TATGTGTGATTTGAT[C/T]CTGTCATTGTGATGT | 55130 |
| rs534958549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27843263 | ATCTGCAACAAATCT[A/G]TGCATGAAAATCTTG | 55130 |
| rs534960491 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ARMC4 | GRCh38.p7 | 10:27953320 | CATAAAACTGCCTTA[A/G]CTATCACAGTTCATT | 55130 |
| rs534962833 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27848947 | GAACACTTTTACACT[A/G]TTAGTGGGACTGTAA | 55130 |
| rs534967657 | snp | A/G | 0.029116 | 0.117091 | intron-variant | ARMC4 | GRCh38.p7 | 10:27967764 | AGTGTGGTAGCGCAC[A/G]CCTGTAATTGCATCT | 55130 |
| rs534981297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27868001 | GTCAATTTCCATATA[C/T]AGTTATTATAAGAAA | 55130 |
| rs534989829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27942409 | GACCAGAAAAATGCC[A/G]TAGGAACTTAATTCT | 55130 |
| rs534992395 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27873869 | TGTAGGTGTCTATTA[C/G]GTCCACTTGGTGCAG | 55130 |
| rs535009300 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27844728 | ATGTCTGGCACACAG[G/T]AAGCTGAAAAAACAA | 55130 |
| rs535015320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27881029 | CATCACTATCAGCAA[C/T]GTGGCTTTCAGCAAA | 55130 |
| rs535022522 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27866665 | TGGTAGAAGGTGAAA[A/G]GAAGTAGGCATCACA | 55130 |
| rs535027140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27943127 | GGGTGAGACACAAGA[C/T]CTATTGATCCTTACT | 55130 |
| rs535037512 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27834909 | GGAAAGTTTTTCTGT[A/C]GTTGTGGATGGAAAC | 55130 |
| rs535045582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983615 | GTGGAATGGGTCACT[C/T]TGAAGCCCATTTCTT | 55130 |
| rs535076364 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27951212 | AATTTATAGATTCAT[G/T]TAAACCAACCAAAAT | 55130 |
| rs535077411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27854664 | GGGAGGCTGAGGCAT[A/G]AGAATTGCTTGAGCC | 55130 |
| rs535079807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27910351 | CGTTGCCTTCATGGT[A/G]TTAAACCTGCAATTC | 55130 |
| rs535099294 | snp | A/G | 0.00398564 | 0.0444627 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999290 | AGAAAACTTAAAATG[A/G]AGCAGAAAGGAAGCA | 55130 |
| rs535141535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27904383 | CAGGAGGCTGAGGCA[C/T]GAGAATTGCTTAAGC | 55130 |
| rs535149920 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27948900 | CCATTAGGTTTTAAA[A/C]GTGCAGAGATTGAAT | 55130 |
| rs535166902 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27817284 | ACTCATGATCTATGG[A/T]TCAGAATTTTTATTG | 55130 |
| rs535173538 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27837858 | TAAAGACAATAGTTG[C/T]TCTGACTGAAATCTG | 55130 |
| rs535211719 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27913809 | CATGAGTCGGAATGG[A/C]TATTATGAAAAAGTC | 55130 |
| rs535216080 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27861374 | CTGAATGTAGTCAGT[A/G]CACTCAAAGGTGACC | 55130 |
| rs535224310 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27823539 | TTTTTAATAGTACTT[C/T]CCTAATAAGATAGAT | 55130 |
| rs535250584 | snp | A/G | 0.000231195 | 0.0107491 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27907702 | GAGTGCCCATGCTGC[A/G]CTGGCCTTCACGTCT | 55130 |
| rs535277438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27923469 | TTATGCACCAAATAA[C/T]ACAGCACCTACTATA | 55130 |
| rs535289128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27916002 | AGAGAATCTCTCTAA[A/G]TGTAGGGGGAAACAG | 55130 |
| rs535369807 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27828183 | CATCTCTGAAGTTTC[C/T]AAGGCAAAAGTCAGA | 55130 |
| rs535373610 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27977525 | CGAGCCAAGATCGAT[A/C]ATGCCACTGCACTCC | 55130 |
| rs535431336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27857598 | ATTTCTGCTGGGCAG[C/T]GCTGCTTTACACCTA | 55130 |
| rs535468895 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27864525 | AGAGTGAGGTGAGAG[C/T]GGGGAGTGAGGTGAG | 55130 |
| rs535474840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27993035 | ATTCTCCTGCCTCAG[C/T]CTCCCTAGTAGCTGA | 55130 |
| rs535490632 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27998725 | GCGGGGCCAGAGAGC[C/T]GCCTCTGTTTCCCGA | 55130 |
| rs535495600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27849115 | CACGTATGTTTACTG[C/T]GTCACTGTTCACAAT | 55130 |
| rs535501394 | snp | C/T | | | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:28000182 | GTCTTGAACTCCTGA[C/T]CTCAAGTGATCCACC | 55130 |
| rs535505581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27863589 | CCATGATGTTGCCTA[C/T]AACTGGTGGGGAAGA | 55130 |
| rs535506270 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27985020 | TGAAAAAGACTCACA[A/G]TGAAATATGTTTTAG | 55130 |
| rs535526525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27991260 | TATTTGACCCCCAGC[C/T]CCCACCCCAAAATTA | 55130 |
| rs535552245 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27903382 | GCATTCCCTTTGAAA[A/T]CCAGCACAAGACAAG | 55130 |
| rs535562644 | in-del | -/TC | 0.00874735 | 0.0655527 | intron-variant | ARMC4 | GRCh38.p7 | 10:27931440 | AAATGTTTACTGCCT[-/TC]TCTCATCATCTACTT | 55130 |
| rs535578368 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27957547 | CTGAAAAGGGGGTTC[A/C]TTGCTTCCTTTAGAA | 55130 |
| rs535583781 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27992534 | TCTCTACAAAAAAAT[A/G]GAAAAATTGACCAGG | 55130 |
| rs535620795 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27909533 | TTAAAAGAAGACTCA[-/G]GGGGCGGGGCCCAGT | 55130 |
| rs535630866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27847865 | GATCCAACTTACAAG[A/G]GATGTGAAGGTACTC | 55130 |
| rs535649649 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27830607 | TGAAACAGTTCTATT[G/T]AGGAAGGTCTCCATT | 55130 |
| rs535653119 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27906870 | GCCTGTCAGGGGGTG[C/T]GGGACTAGGGGAGGA | 55130 |
| rs535686695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27990701 | TGTAACCTTAGAGAT[C/T]ATGTAAATTCAGCCT | 55130 |
| rs535694866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27922742 | GAAACCCTGTCTCTA[C/T]TAAAAATACAAAAAT | 55130 |
| rs535716401 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | ARMC4 | GRCh38.p7 | 10:27875768 | CTCACCCAGGAAGCA[A/C]AAGGGGTCAGGGAAT | 55130 |
| rs535726940 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27969910 | CAGGAGTTTGAGACT[A/C]GCCTGGCCAACATGG | 55130 |
| rs535729105 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27881433 | TGGGAGAATTGAGAC[A/C]AGCCTGGGCAACATA | 55130 |
| rs535746873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27868588 | ACACACGAACAGAAA[A/G]CCAAACAACACGTGT | 55130 |
| rs535762074 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27821752 | TATGAAATTGGTATA[A/C]ACTTTTTTGGTATCT | 55130 |
| rs535792868 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27878325 | CATTTGGTTAAAATT[A/C]AACTAATGGGAAAAA | 55130 |
| rs535794065 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27929953 | AGTTTTCTTCTGTTA[C/T]ATCTTTACTTAAGAT | 55130 |
| rs535794343 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27985311 | AAAGTCCATTCAGAC[A/G]TGTTTCTTTCATTAA | 55130 |
| rs535803134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27961403 | GATGAATCTTGCATC[C/T]TCAGGGTAATAAGAC | 55130 |
| rs535825653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27843960 | ATCCCAGCACTTTGG[A/G]AAGCTGAGGTCGGAG | 55130 |
| rs535836886 | in-del | -/A | 0.487995 | 0.0765403 | intron-variant | ARMC4 | GRCh38.p7 | 10:27824139 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 55130 |
| rs535853800 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27929133 | TGTACAGAAAAATAC[A/C]AAGCATTAACAAATG | 55130 |
| rs535858644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27930492 | GCACTCCAGCCTGGG[C/T]GATAGAGTGAGACCT | 55130 |
| rs535888081 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27977110 | TCATAGATATAGATT[A/G]GAAAGGTAAAATTGA | 55130 |
| rs535889713 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27921745 | CAGTCCAAAAAAAAA[A/G]AAATCAAGTAATTTA | 55130 |
| rs535917244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27897730 | GGCAGTTCCTGGTGA[A/G]AGATGTGATCAAGCA | 55130 |
| rs535962667 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27968587 | AGGCTCAGACAGATA[C/T]ATAACTTTGCCAGGA | 55130 |
| rs535975794 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27931735 | GCAATGATAACATTT[A/T]GAAGGAATTTCAAGG | 55130 |
| rs535985674 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944013 | CTGTCCTATTTCTTC[-/A]AAAAATGAGTTTGAA | 55130 |
| rs535987693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27975930 | ATTAAATCTGATAAT[A/G]TACATAAAAGATTCA | 55130 |
| rs535997175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27943219 | CAGGATTCTGGTATT[C/T]TTCTTTTGATGCCAG | 55130 |
| rs535997889 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27920383 | AGAAGCCCACTCACA[A/G]TAAATAGTACTGAGA | 55130 |
| rs536014884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27841585 | ATTTTTAGTAAAGAC[A/G]GGGTTTCACCATGTT | 55130 |
| rs536017875 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27949011 | TTTTTAATTACTTCA[A/T]ATAAAATATTTGAAA | 55130 |
| rs536045916 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27848043 | ATCAAGCTACCAATG[A/T]CTTTCTTCACAGAAC | 55130 |
| rs536066917 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27847508 | TCCCTTTGAAAACTG[G/T]CACAAGACAGGGATG | 55130 |
| rs536079968 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27833100 | ATACCACAAAATACA[C/T]AATGAAGGGTAGTTC | 55130 |
| rs536081899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27854342 | CCGTATGATCCAGCC[A/G]TTCACTCCTAGGTAT | 55130 |
| rs536107722 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27850932 | CGAGTTGAGGAGACA[C/G]AGCTGGAAGTCTGGG | 55130 |
| rs536154294 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27813868 | AGAGGTGACAGGATG[G/T]AATAAAAGGTAAGGA | 55130 |
| rs536165559 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27902166 | CTCTCTCAAAACCAC[A/T]CAACTAAATGGAAAC | 55130 |
| rs536177674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27955499 | GCAGCTCCCTTCTGT[A/G]TGGCCTGGAGCAAAG | 55130 |
| rs536182654 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27821229 | GGGTATGAATATTTG[A/G]GAAGTACCCCCAAGA | 55130 |
| rs536191404 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27813273 | TCTTTCAAAACAGAC[C/T]TAGCCAACTTTTCCA | 55130 |
| rs536241104 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27913200 | AATTACGTGTCGCGG[C/G]GGTTTGGTGTACAGA | 55130 |
| rs536248514 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27877834 | CAGGCTAAATTTTGC[A/C]ATTTATAAAGGACTT | 55130 |
| rs536287724 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27874457 | CCTAGCATCGATGGT[A/C]TTTACATTTTGGCAT | 55130 |
| rs536320835 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ARMC4 | GRCh38.p7 | 10:27873568 | GTGTCTTTGTTCTCA[C/T]TGTTTTCAAAGAACA | 55130 |
| rs536334358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27819752 | CCTCAAAACCCATAC[C/T]CTTGACTATGGTTTG | 55130 |
| rs536392232 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27928552 | TGCCTGTTCACTTAT[C/G]TATGACATGCCCTCA | 55130 |
| rs536469036 | in-del | -/C | 0.00795532 | 0.062565 | intron-variant | ARMC4 | GRCh38.p7 | 10:27994406 | GGTAATACGGAAGTA[-/C]CCCCATACATTTATA | 55130 |
| rs536478824 | snp | C/T | | | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27857853 | GCCTGTCAACATTCA[C/T]TCATTGGCAGCTGCA | 55130 |
| rs536541378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27896443 | ATTCAAGTACATAGA[C/T]TGATAGGTAATAGAT | 55130 |
| rs536559074 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27862033 | AAGTCTTCTAGCTCA[A/G]GAATGCCATCGACTG | 55130 |
| rs536559840 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27989738 | CTTTGGTCCCAGCTA[C/G]TTGGGAGGCTGAGGT | 55130 |
| rs536562196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27887085 | CAAAATGGATTTTAA[A/G]AAAACAATTCTACAA | 55130 |
| rs536566758 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27895587 | AGCCACCACACCTGA[A/C]CTAAACTTTAATTAA | 55130 |
| rs536574661 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27940391 | TATATGTGTATATAT[A/C]TCACAGGTACTGATT | 55130 |
| rs536588689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27925798 | AAGACAAAGAGGATC[C/T]CTATCTCCACTACTA | 55130 |
| rs536589804 | in-del | -/ACTTA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27963605 | TTTTCCCCCCACTGG[-/ACTTA]ACTTGTTGCTAAGGC | 55130 |
| rs536599932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27955648 | TTCCTACAACAAAAA[C/T]TCATACAACTTCCAA | 55130 |
| rs536604077 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27954170 | CAGCCTCTGTAACAG[A/G]CCATGAGTGTGTGTT | 55130 |
| rs536634995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27922352 | GCTCCAAACTAAGAC[C/T]ATAGAACTTAAGCTA | 55130 |
| rs536655475 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27829810 | AGTTTTAGAACAGAA[G/T]AATACTTCTTCCTCT | 55130 |
| rs536658114 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27903642 | AAGTCATAAGCATTC[C/T]TATACACCAATAATA | 55130 |
| rs536658757 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27874237 | ATACCTTTATTTTGA[G/T]CCTATGTGTGTCTCT | 55130 |
| rs536683302 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27907022 | TATAATTTAAAAAAA[A/C]ATTCAACAGGCAGAA | 55130 |
| rs536735763 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27848084 | TACTTTAAAGTTCAT[A/G]TGGAACCAAAAAAGA | 55130 |
| rs536747246 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872854 | AGGCTTTGGTATCAG[C/G]ATGATGCTGGCCTCA | 55130 |
| rs536794351 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27845705 | AGACACACATAGGAT[A/C]AAAATAAAGGTATGG | 55130 |
| rs536797127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27835608 | TCAGAAGCCTTAACA[A/G]TAACATAAACAGTCG | 55130 |
| rs536802021 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27857969 | TGCCAAAATACTGGA[C/T]AAAATTTACATGCAT | 55130 |
| rs536802653 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27966211 | TGGAAGAGGGAAAGC[C/G]TGAATTCAAGCATCT | 55130 |
| rs536827777 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27935911 | AGCATGCTACATAAA[G/T]GTAAATATTTGAAAA | 55130 |
| rs536840387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27840420 | GTGCCTTCCCAGCAC[A/G]TCATGAACGCCCTTG | 55130 |
| rs536860858 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27929344 | TGACTTTTTATGTGA[A/C]AGATGATAAAATTTG | 55130 |
| rs536937751 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27980616 | CAAATCAAAGCCCCA[A/G]TGGGATACCACTTCA | 55130 |
| rs536964995 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27812885 | CTAACTGCTATTTTT[-/G]GGTCTGCTTCTGAAA | 55130 |
| rs536974711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27973501 | CCCACCCTCCAATCT[C/T]AAGTAGGCCCCAGGG | 55130 |
| rs536985177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27839249 | CTATAGTAAACTTCT[A/G]AAGATATATAAGTAA | 55130 |
| rs536985892 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27942322 | TTAAATGTACGTATA[G/T]GTCACAGTCATTTCA | 55130 |
| rs536988483 | snp | C/G | 5.11496e-05 | 0.00505689 | intron-variant | ARMC4 | GRCh38.p7 | 10:27935301 | TTTGTATAAGGTTTG[C/G]TAAAAATTACTAAAT | 55130 |
| rs536997205 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27933560 | ATAGTCCAGGTAAAA[G/T]ATGACAGAGCCCAAC | 55130 |
| rs537020855 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27821801 | TTTCTTTCCAACTAT[A/T]AAGACATGTTTTAAT | 55130 |
| rs537043566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27914585 | TAAAGGCAGAATATA[C/T]GTTTAATCTGTTCCC | 55130 |
| rs537082129 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27875691 | TGAGTCTTGTTGGAC[A/C/G]GTGGCTGCAGGACAG | 55130 |
| rs537084299 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27844477 | AAGCATAGGAGTCCA[C/T]ACATATATGTGCATC | 55130 |
| rs537084414 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27869254 | ATAGTTAACAAAAAA[C/T]TCAAGGCAACAAATA | 55130 |
| rs537099891 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27815039 | TAGCCCCCATTTCCA[G/T]AAGATGACCAATAAG | 55130 |
| rs537100612 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27921776 | CAAAGGCAAAATAAT[A/T]AGACAAGCATCAGAC | 55130 |
| rs537105170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27996304 | TACAAAGATTAGACT[C/T]GGAGATTTTACATTC | 55130 |
| rs537105189 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27952583 | CCCTGGTGTGTGTTG[A/T]TACCCTCCCTGTGTC | 55130 |
| rs537112767 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27907093 | CCTATAGAAAAAATG[C/T]TAAGAGAAATAGGCT | 55130 |
| rs537117673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27868458 | TGATACACTGGATAA[A/G]GAAAATATGGTAGAT | 55130 |
| rs537127801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27969209 | CACAGCCCTATGTTT[C/T]ACATATTGAAGAAAC | 55130 |
| rs537128494 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27963306 | GCCACTGCACCCGGC[C/T]TGTCCCAGGCACTTT | 55130 |
| rs537147748 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27820961 | AATTTTGCATTTTTA[C/G]TAGAGACAGGGTTTT | 55130 |
| rs537164606 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27962164 | AATAATCATAATAAA[C/G]AAAACAGTGAGAAAT | 55130 |
| rs537184643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27947439 | TACCACTCTCCAGCA[C/T]GGGCAACAGAGTGAG | 55130 |
| rs537189840 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27923478 | AAATAATACAGCACC[C/T]ACTATAGAAGATGTA | 55130 |
| rs537257085 | in-del | -/A | 0.494388 | 0.0526741 | intron-variant | ARMC4 | GRCh38.p7 | 10:27890773 | GTATATATATATTTA[-/A]AAAAAAAAAAAACTT | 55130 |
| rs537258921 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27952074 | CTGAGATGCCAACTC[-/A]AAAAAAAAAAAAAAA | 55130 |
| rs537272466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27842166 | CTTTGTTTCCTTTAC[A/G]GCATTCAGCACACTT | 55130 |
| rs537273869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27913239 | TTACCCAGATAATAA[A/G]CATGGTACCTGATAG | 55130 |
| rs537305837 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27848141 | CCAAAAGAACAAAGC[C/T]GGAGGCATCACACTA | 55130 |
| rs537325890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27880167 | AATTATACAGGCCAG[A/G]ACTCCCCTGTCCTGC | 55130 |
| rs537329299 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27839874 | TAATAGTACACCTCC[C/T]ATAATCACAAAGTAT | 55130 |
| rs537346751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27975167 | GATCCCTTGTTTTAT[A/G]TGCTCCAAGTAAAAC | 55130 |
| rs537351687 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27878311 | TAAAACAGCAAATAC[A/G]TTTGGTTAAAATTCA | 55130 |
| rs537360625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27888492 | AATGTCTATTCATGT[C/T]CTTTGCCCTCTTTTT | 55130 |
| rs537399880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27887921 | ACAGTTGTACACCAA[C/T]AAGTTGGATAACCTA | 55130 |
| rs537445325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27996850 | CACAGTCATTCTGTG[C/T]AAGGCTGGACATCTG | 55130 |
| rs537455418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27941883 | TATAAGGGAATAATA[A/G]CCTAGGCTAGGTAGA | 55130 |
| rs537456902 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27830108 | TCTTGCTCCCCATAG[A/C]GATCCTTGAAGTACC | 55130 |
| rs537472546 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARMC4 | GRCh38.p7 | 10:27861182 | TTTTTAGTAGAGAAG[A/G]GGTTTCACCATGTTG | 55130 |
| rs537475744 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27842301 | TGGTGAATAGAAGGA[C/T]AGGTCCTGCCCATGT | 55130 |
| rs537489766 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27973645 | GGCTGTGTAGTATTC[C/T]ATGGCATATATGTAC | 55130 |
| rs537497770 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27846295 | CGCTCAACTACATGG[A/T]AACTGAACAACCTGC | 55130 |
| rs537541703 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27954301 | TAGGGGAAAAGCATA[C/T]TTTAAGGAACAAAAA | 55130 |
| rs537541854 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27961168 | ATTCTATGGGTTGAG[A/T]AAATTAGGGCTCAAA | 55130 |
| rs537556542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27980799 | AATACAGAATTACCA[C/T]ATGACCCAGAAATTC | 55130 |
| rs537557463 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27867968 | AGAAAAAAAAAAAGC[A/G]GTATAAAAAAGACTC | 55130 |
| rs537587981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27820412 | CCACTGCATAAACCA[A/G]TGGACTGTGAGTGTC | 55130 |
| rs537601320 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27960586 | AACTCCTGACCTCAG[A/G]CGATCCACCCTCCTC | 55130 |
| rs537638046 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27859773 | ATATTCTAGTTGGTT[G/T]GCAATGTGTAGGTAA | 55130 |
| rs537638168 | snp | A/G | 6.60131e-05 | 0.00574476 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27995101 | TCCAGTTCCATGTCC[A/G]GCAGCAGTCCACTGC | 55130 |
| rs537651721 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27834209 | AAATGTAGTGATTGA[A/T]ATAATCTAGGAGGTT | 55130 |
| rs537691284 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27873800 | CAATTTTGGAATAAG[G/T]GTGATGTGGTGCTGA | 55130 |
| rs537727701 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27869518 | AAAAAGACTAAGTCA[C/T]TTTTTTTTCTTTTTT | 55130 |
| rs537747146 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27958791 | ACTTTTATTTTTCCA[C/T]CTTCACCAATGAGGA | 55130 |
| rs537753530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27865455 | CCTACACATCTTCAG[C/T]TGCCAACTAAGGTAT | 55130 |
| rs537772166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27967153 | AAATGATCTATCTCA[A/G]TCAAGACCACACATA | 55130 |
| rs537789122 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27841460 | GAGTGCAGTGGTGCG[A/T]TCTCAGCTCACTGCA | 55130 |
| rs537808529 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27958317 | TACAAGGACTTATCC[G/T]AAATAGTTGAAAAAA | 55130 |
| rs537822556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27825106 | TGCTTGGGCTGAAAA[C/T]CTTGGTGTATCCTTG | 55130 |
| rs537823725 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27832674 | AATTACCAGAGCACA[C/T]GTGACCAGGAATGCT | 55130 |
| rs537825572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27840480 | AGTCTTGGAAGCCAT[C/T]TTGTAAAGTATCACA | 55130 |
| rs537840241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27962737 | AGAGGTCCCTCATGC[A/G]CACGCACACTCATCA | 55130 |
| rs537857384 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27934387 | ATATCTTTATAAAAT[A/G]TAAAGATATATGTCT | 55130 |
| rs537860728 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27832261 | ATTAATCACTCTTTT[G/T]CCTGGACACAATGTC | 55130 |
| rs537894959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27900152 | TGTTCTGCAGCCTCC[A/G]CTCATGATACCCAGG | 55130 |
| rs537899009 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27852891 | GCTTGAACCTGGGAG[A/G]TGGAAGTTGCAGTGA | 55130 |
| rs537907976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27924955 | GCCCAGGTAGTCCCA[C/T]TGCTCAATAAACTGT | 55130 |
| rs537918232 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27908608 | AAGGGCATCAAAATT[C/G]CTTTGATTTTTAATC | 55130 |
| rs537921276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27901129 | CTCTGCAAAAACTCT[A/G]CAAGCCAAAAGAGAG | 55130 |
| rs537940666 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27971886 | ATGAACAAAAACAGA[C/G]AATTCACTGCCAGAA | 55130 |
| rs537955908 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27965063 | GGGAGTGTGTAGGCC[A/G]AGATTTGGTACTGGT | 55130 |
| rs537973642 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27964742 | TTTTGTAGCTCAGTA[A/C]CTTGTCCACTTTGGT | 55130 |
| rs537982087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940430 | GTCCTATCAGTTGGA[C/T]CTTCTCTTTCTCATA | 55130 |
| rs537983937 | snp | C/T | | | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27936568 | ATTTCTATTCTTTTC[C/T]TTTCTATTCTAAGAA | 55130 |
| rs537998535 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27838383 | GTCAAATAGCTGCCA[A/G]TTAATATAATGGATT | 55130 |
| rs538027317 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27990028 | CTATCAAAAACTCCA[C/G]TGACCTGATGGAGAA | 55130 |
| rs538040864 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27882478 | GAAATGGTGGAATAG[A/T]GACCTCCAAAAATCT | 55130 |
| rs538048725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27946535 | GGTGGGAACTTTACA[A/G]TTCCTCCCTTCTAGC | 55130 |
| rs538100801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27979117 | CGGGAGCTTGAGGCA[C/T]GAGAATCACTTGAAC | 55130 |
| rs538118412 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27826770 | CTGCCTCTTTCACCC[C/T]CCTTCCTGCTCTTGC | 55130 |
| rs538129622 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27899464 | ATGCCAGCGAGACAG[A/G]ACTGTTCACACTCCT | 55130 |
| rs538139187 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27905926 | ACCCTGGAAGAAAAC[A/G]TAGGCAATACCATTC | 55130 |
| rs538142860 | snp | G/T | 0.0221141 | 0.102801 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872404 | TATGTTGAATAGCAG[G/T]GGTGAGAGAGGGCAT | 55130 |
| rs538183053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27887579 | GACCATATATGAAGC[C/T]GCAAAACAAGTCTTT | 55130 |
| rs538210058 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27979317 | TCCAGGAAGTCCTAG[A/C]CACAGTAATTAGTCA | 55130 |
| rs538225441 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27841890 | CTCCTGAGTAGCTGG[A/C/G]ACTACAGGTATGCAC | 55130 |
| rs538229280 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27934594 | CTTGTCTCTTCCCCT[C/T]ATCAGTTCACAGTTC | 55130 |
| rs538243644 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27923490 | ACCTACTATAGAAGA[C/T]GTAAGAAGATTTAGA | 55130 |
| rs538266717 | in-del | -/AACA | 0.0103295 | 0.0711199 | intron-variant | ARMC4 | GRCh38.p7 | 10:27947544 | TGCACAAAAAGAAAG[-/AACA]AAGAAAATAAGAAAA | 55130 |
| rs538270873 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27911086 | GATTTTTTTCCAAAA[C/G]GAACATCGCCGCCGT | 55130 |
| rs538276501 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27878351 | AAAAATATTGAGACA[C/T]TATTTACAGATTAAT | 55130 |
| rs538285631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27974945 | ATTCTCACTGTAGAG[A/G]TCTTTCACCTTTCTG | 55130 |
| rs538291712 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27967356 | CGAACTGTGATATCA[C/G]TAGAGCCCACTGACA | 55130 |
| rs538291919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27880268 | TTTAGATATAAATTT[C/T]ACCTTGTGAAACTTT | 55130 |
| rs538302455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27889623 | CATTTTGGTGTGCTG[C/T]CCCTCAGTCCCACTG | 55130 |
| rs538307749 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27878448 | CTTGCCTCCAGCGAA[A/C]AGCACTGGCAGTTTT | 55130 |
| rs538311646 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27831216 | TCTGATCTATCAGAA[A/C]AATTCCTTGTTCTTT | 55130 |
| rs538330145 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27815827 | TCTTCTAAATTTCTA[C/T]CTCCACCCCAGAAAC | 55130 |
| rs538335788 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27988463 | CCACCTCAGCCCCCA[A/G]GTAGCTGGGACTAGA | 55130 |
| rs538358661 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27886125 | TAAAGTAATAATGAC[C/G]AAAAATGTCCCAAAT | 55130 |
| rs538391767 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27884825 | TATATGGGGGAAAAA[A/C]ATTAAAAGCATACAT | 55130 |
| rs538391997 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27847459 | ATGACATACCCACAG[A/C]CAATATCATCCTGAA | 55130 |
| rs538393617 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27894088 | AGATTGACATTGCAG[A/T]GTGCAAATGTGCCAC | 55130 |
| rs538411071 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27845541 | GAACCAGCTAACATC[A/T]CAATGACAGGATCAA | 55130 |
| rs538413563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27895717 | CCTTTTCATCATCAC[A/G]CAAAGTGCTATTAAT | 55130 |
| rs538428870 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27853621 | TTACAGGCATGAGCC[A/C]CTCTGCCTGGTCCAG | 55130 |
| rs538428971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27847112 | AAAGCCTGGCAGAGA[C/T]ACAGAAAAAAAAGAG | 55130 |
| rs538459530 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27838760 | TATACTTTATTTTAC[C/T]ATACTGTTTGTGTAT | 55130 |
| rs538465162 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27840970 | CAGGGGTACAGTGAA[A/G]ATTAAATGAAATAAG | 55130 |
| rs538465665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27853018 | CACATTAAATGTAAA[C/T]AGTGTAACCACTTCC | 55130 |
| rs538471861 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27981226 | TTCGAGAGACGAAAA[A/T]GACTTGGAAATTGAC | 55130 |
| rs538527097 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27893444 | CTGAAGTAGCAACAG[C/T]TTGTCTAAAGGCGTA | 55130 |
| rs538539621 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27978520 | AACTGGAGCCGGGCA[C/T]GGTGGCTCACACCTG | 55130 |
| rs538541699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27899867 | AGAACACCTGGGGGA[A/G]GGGGTGGCAGTGGGC | 55130 |
| rs538544945 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27987024 | GAGAGAGTGGATTCA[C/G]AGGCCAGCCCTTGTC | 55130 |
| rs538596496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27834341 | TCCAAAGGCGCTATC[C/T]CTTGGCCTTCTGGAA | 55130 |
| rs538599282 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27884923 | TCCCAGGCTCAGAAA[C/T]TTGTTAATTAGTGAA | 55130 |
| rs538599598 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27952745 | GTTTATTTGCTCCAT[A/C]GTTTAACAGCTCTGG | 55130 |
| rs538620013 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27826864 | CAAGACCTCCTTTAC[C/G]TCCCCTTCCAGCTAG | 55130 |
| rs538624540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27927775 | TGATGCCTGTTTCTT[C/T]ACAGAGACTTTTTCT | 55130 |
| rs538627988 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27818932 | TCACAGCATCTTGGA[A/T]CTGTACTCTGACTCT | 55130 |
| rs538648129 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27861304 | GCTGAAGGAACTAGA[C/T]TTTTGGTGGGTCACC | 55130 |
| rs538650600 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ARMC4 | GRCh38.p7 | 10:27859274 | TTAAAAGATGCTTTG[A/G]CCAGATTTTTGCTTG | 55130 |
| rs538656397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27825975 | TCCTCCAAGCACCTC[A/G]CCTCTAACTTCAGAC | 55130 |
| rs538661272 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27920425 | TCATCTATTAATATG[C/T]GTGCATATCACAACT | 55130 |
| rs538711975 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27918824 | AATTGGAAAAAATAA[A/G]GTTAGCAAGTTTGCC | 55130 |
| rs538712290 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27888607 | ATTTTCTCTCATTCT[G/T]TAGGTTTGTCTATTT | 55130 |
| rs538723178 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27835567 | TTGACTGCCCCCAAT[C/T]TTAAGGACTGATAGC | 55130 |
| rs538772147 | snp | C/T | 0.000121751 | 0.00780132 | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27958996 | ATAAAGATAATGGAC[C/T]GGGACTCTTGGGAAA | 55130 |
| rs538824661 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27932877 | AGAATGTAATCCCCA[C/T]GACAGCAGGAGCTTT | 55130 |
| rs538826286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27925028 | CTTTTGTGAAGCAAG[C/T]ATAACATTGATAACT | 55130 |
| rs538830627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27832339 | ACTTGATTTTATCAC[A/G]CATGCCCTCTTTCAA | 55130 |
| rs538855361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27989114 | GGAATGCAACCCTGC[C/T]GATACCTTGATTTTA | 55130 |
| rs538862819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27925748 | CTTTTACTTCATAGA[A/G]AGACACTAGAGGCAT | 55130 |
| rs538882732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27859889 | TATCTATTGTTGTTA[C/T]GGTTTAGACTAACAA | 55130 |
| rs538889575 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27850078 | ATGATGTCACATCAT[A/C]TATTGATGGTGTAGG | 55130 |
| rs538893137 | in-del | -/ATGACTTG | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27823054 | TGCTAGAAATGGAGA[-/ATGACTTG]ATGACTGGCTGGGTC | 55130 |
| rs538907988 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27913449 | TATGCATGTTGTTGC[A/C]AAAACAATTACAACA | 55130 |
| rs538922149 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27813333 | AGGCCATTTATTCCT[C/T]ATCAGGCTGTCAGTA | 55130 |
| rs538956905 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27819630 | AGGTGTGGTCACGTG[C/T]GCCTGTAGTCTAGGT | 55130 |
| rs538986745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27932237 | CACCACGTCATTAGC[C/T]TATAGTTGGGCAAAA | 55130 |
| rs538994077 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27916273 | TGGGGAACTAGAGCC[C/T]GAATGGGGTGAAGAG | 55130 |
| rs539018185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27867358 | GATGGTGCTGGGGTG[C/T]TCTGTTAGGCCTGAG | 55130 |
| rs539050175 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27848665 | AATCTACCCATCTGA[C/T]GAAGGGCTAATATCC | 55130 |
| rs539052706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27912520 | GCTCGCCTGCCCATT[A/G]AGGCCATATATATGA | 55130 |
| rs539066046 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27906005 | TGGCAACAAAAGCCA[C/G]AATTGACAAATGGGA | 55130 |
| rs539071706 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27965838 | TTATAAAAAGACTTA[C/T]GAGAAAGTACACTTT | 55130 |
| rs539073800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27938875 | AAAGTGCTGGGAATA[C/T]GGGGACTGCAGGGCC | 55130 |
| rs539088220 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27987106 | TCCAGAAGCTGAGAA[G/T]GTTCTCTTTCAAACC | 55130 |
| rs539109478 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872491 | GATATTGGCTGTGGG[G/T]TTGTCATAAATAGCT | 55130 |
| rs539109789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27878948 | TCAATTATTACCCTT[A/G]TCCTTGTGAACCAAA | 55130 |
| rs539113185 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27904500 | AAAATATAAATAAAT[A/G]AATATAAAAAGTCCA | 55130 |
| rs539137061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27966163 | CAAAAGCCAATTTGT[A/G]TGTAAAACACTATGA | 55130 |
| rs539204683 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27838969 | CAACATGTGCCAGCA[C/T]CATCTTATGCCAATC | 55130 |
| rs539249568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27916642 | TATGAAGATTCACTT[C/T]CACTTAATGAATAGT | 55130 |
| rs539263481 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999346 | TTACATTTTTCCATA[A/G]GCTTCCAGACAAGTG | 55130 |
| rs539268559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27887021 | AAAATAAGTGCTTTC[C/T]TATACTTTAAATGTA | 55130 |
| rs539291253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27871071 | GTGAGATGGTATCTC[A/G]TTGTGGTTTTGATTT | 55130 |
| rs539311381 | in-del | -/C | 0.00636936 | 0.0560724 | intron-variant | ARMC4 | GRCh38.p7 | 10:27906764 | AAACTAATACAGGAA[-/C]AAAAAACCAAACACC | 55130 |
| rs539340602 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27972213 | TTTTAGAATTTTACT[C/T]AAAGGAGACGTGACA | 55130 |
| rs539346701 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27979792 | TGGCAATACTATGTA[A/C]AGCAATTCATAAATT | 55130 |
| rs539360393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27884733 | ACAGGCACAGAAGTA[C/T]AACTGAATGCCTAAG | 55130 |
| rs539360420 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27876314 | AGGGGCAGACTGACA[A/C]CCCACACTGCCGGGT | 55130 |
| rs539433327 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27837045 | AGGATTTCTGGGACT[C/T]GTAGGAGTGTAACTG | 55130 |
| rs539459319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27850301 | AACAAAAAAATTAGA[C/T]GGCCGTGGTGGCAGG | 55130 |
| rs539460955 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27858253 | GAGAAAGGAAACACA[C/G]GTTGTTATGCTTCCC | 55130 |
| rs539478121 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27865190 | TTCTCCAACCTCCCC[A/C]ACATATACCCTGAGC | 55130 |
| rs539491041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27978195 | GCAATAAATTAATGA[C/T]AGATGCAAAAGCATA | 55130 |
| rs539495813 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27883991 | AAAAGGAGAAAGAGA[A/T]GAGAAAGAGGCAGAA | 55130 |
| rs539515825 | snp | C/T | 2.30651e-05 | 0.00339588 | missense, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27985077 | ATTGCTTAAGCAGCA[C/T]AGCAATCTTCATCTT | 55130 |
| rs539537047 | snp | G/T | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27961028 | TATATGCTATCTGAC[G/T]TGAGAGAAATGAAAA | 55130 |
| rs539556380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944504 | AATTCCGAGTATACC[C/T]AAAATCCTTCCCCAG | 55130 |
| rs539565969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27951882 | GAGTTCGAGACCAGC[C/T]TGACCAATATGGTGA | 55130 |
| rs539566489 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27993694 | CTTCAAACAACTCAG[A/G]GAGAAGGCTGACCAA | 55130 |
| rs539571697 | snp | A/T | 0.00398564 | 0.0444627 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:28000404 | CAGAGAAGCCCTTTT[A/T]AAAATGGGTGGATTA | 55130 |
| rs539619289 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27950036 | GGACCAGAGGCCTCT[G/T]GTTCTGTCCCTACCC | 55130 |
| rs539637714 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27998607 | CTAGGGCCGAGGCAG[A/G]GTCTCGCGGGGAGGA | 55130 |
| rs539651653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27823703 | CTCATTTTCTCTGCT[A/G]CAGTTCCTGTTGGAC | 55130 |
| rs539673353 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27856110 | AACTTGGATATCTCT[A/T]AGACTTCTCATATTT | 55130 |
| rs539674836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27916078 | GTGGTGCAACCCAAC[A/G]CGGGAAGTCAGAACC | 55130 |
| rs539687853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27876061 | GGAAGCTCGAACTGC[A/G]TGGAGCCCACTGCAG | 55130 |
| rs539698008 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27963660 | ACTATTTATGGTCTT[A/T]ATTCCTCTCATTCAG | 55130 |
| rs539723200 | snp | A/G | | | downstream-variant-500B, intron-variant | ARMC4 | GRCh38.p7 | 10:27811924 | TGACAGTTATACGTT[A/G]TCCTTTCAGATGTTT | 55130 |
| rs539733790 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27974501 | TCTTTTCCCCATTGC[C/T]TGTTTTTGTCAGCTT | 55130 |
| rs539734205 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27939122 | AATAAGTAAACCAGT[A/G]AAAAGATAAAACAGG | 55130 |
| rs539742731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27956354 | GAAGCTGGCATCCCA[C/T]AGGGAGGAGGTACAT | 55130 |
| rs539765882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27837530 | GTCATTAGTGTGTAT[A/G]TTTTATGTTCTTATA | 55130 |
| rs539780883 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27949707 | CAATGTAATTTACAA[C/T]GATGTCATTTATAAA | 55130 |
| rs539783936 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27872765 | CAGTTTGCCAGTATT[G/T]TATTGAAGATTTTTG | 55130 |
| rs539820463 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27931060 | CAAAACTGGGTCTCT[G/T]ATGGCAAAGTCTTCA | 55130 |
| rs539856529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27923576 | TCAAGTTCACACAAA[A/G]TAATAAGATAGAAGA | 55130 |
| rs539919674 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27889484 | TTGCTCAGTAAGAAA[G/T]CTGGGTGGCCAGGCT | 55130 |
| rs539925607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27978732 | AGGAGGCAGAGGTTG[C/T]AGTGAGCCAAGATCA | 55130 |
| rs539932216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27894314 | AATACAACATGAGAC[C/T]TCAAAAAAATTCCAA | 55130 |
| rs539958762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27860085 | TTATGGAATGATTAT[C/T]TTACTAAGTACATTT | 55130 |
| rs539987737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27931836 | GCTTCGCAAGAGTAA[A/G]TTCTAATCTATAATA | 55130 |
| rs540015576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27991415 | AAAAGGACAGAAGGC[A/G]GTTGATGAAACATAA | 55130 |
| rs540036881 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27993268 | ATCATATTTCAAAGC[G/T]TAGGAAAAAAGCTGA | 55130 |
| rs540038241 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27998236 | ATGCAGAAGTTACTC[A/G]GTAAGACCGACAGAA | 55130 |
| rs540040384 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27870329 | GCCAGATTCCTGTAC[A/G]TCTTTGAATCTGTTA | 55130 |
| rs540065893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27898637 | TTTCCCTGTAAACAA[C/T]ATTATTTAAATTTGG | 55130 |
| rs540070814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27899608 | TCCAAAGTCGACCTG[A/G]CATGCTCAAGCTTGG | 55130 |
| rs540091458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27986716 | ATGATTAGGTACTTC[C/T]ACTCATAAGAAACAT | 55130 |
| rs540095267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27992517 | AACATGGTGAGATCC[C/T]GTCTCTACAAAAAAA | 55130 |
| rs540097174 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999439 | ATTTGAGGCTTACAT[A/G]TTTCTCTCCAAAAAA | 55130 |
| rs540102328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27909067 | CACAATGAAGGATTT[A/G]CTTTTCAAATTTAAA | 55130 |
| rs540115299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27904205 | GTGATAGGGCTCCTG[C/T]AATGTGGTGCACATT | 55130 |
| rs540139555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27863860 | CTGGAGCACAAAATA[A/G]GAAAGGCAGCATGGG | 55130 |
| rs540139988 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27903447 | ATTGGAAGTTCTGGC[A/C/T]GGGGCAATCAGGCAA | 55130 |
| rs540151233 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27950737 | TACTACAGGCATGCA[C/G]CACCATGCCTGACCC | 55130 |
| rs540179295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27886596 | TTTGGTAAAAATAAA[C/T]AGATGAACAAATAAA | 55130 |
| rs540197576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27932379 | TTTCTACTGACTGCG[C/T]ATTTTTGCACCATCA | 55130 |
| rs540221262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27957386 | CAGAGGTAGGGAGGC[A/G]AGCCTGTGCACACTA | 55130 |
| rs540228213 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27911695 | AACAAAACCTCTTTC[A/G]CAAATTCTCTGGCAT | 55130 |
| rs540231938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27941486 | CAAGATCCTGCCCCC[C/T]GAACCAAAAAAAAGA | 55130 |
| rs540232080 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27925137 | AAAATGCTAAATATT[A/C]GCTAACAGAGTCCTA | 55130 |
| rs540252884 | snp | G/T | 0.00517822 | 0.0506191 | utr-variant-5-prime, intron-variant | ARMC4 | GRCh38.p7 | 10:27998887 | GCGGCCGCGCACGCC[G/T]GCGCCCTTGTGGGAG | 55130 |
| rs540255312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27845741 | GACCTACCAAGCAAA[C/T]GGAAAACAAAAAAAG | 55130 |
| rs540271932 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27870670 | TAATCCATGTCCCTA[A/C]AAAGGACATGAACTC | 55130 |
| rs540275878 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27879125 | TTTCTGCTTCTCTAG[A/C]CTGATTTGACATAAT | 55130 |
| rs540276556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27964445 | AGAGAGTGTGAAATA[C/T]GTGTTTTAGTTCTGT | 55130 |
| rs540312658 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27970605 | GAATACAAAGAGGAG[A/C]AGAAAGGAATCAACC | 55130 |
| rs540337887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27971605 | AACCAAAACCCTCTA[C/T]TGACTAAAACACATC | 55130 |
| rs540361457 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27939096 | ATACACAAAAAGTTA[G/T]TGTAGATTACAATAA | 55130 |
| rs540386125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944524 | TCCTTCCCCAGTTAA[A/G]TTTTTTAAGAAATCA | 55130 |
| rs540412442 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27830717 | GGAGTGGATTGTATC[G/T]CTAAGCCTTTTCCAG | 55130 |
| rs540418366 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27904542 | GAGATTTGACTTGCC[A/C]CTTTTATCATATACT | 55130 |
| rs540420510 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27850377 | GTGAACCTGGGAGGC[A/C]GAGCTTGCAGTGAGC | 55130 |
| rs540425420 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27932228 | GATGTAAGCCACCAC[A/G]TCATTAGCCTATAGT | 55130 |
| rs540427101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27883316 | CCTCTGGAGTCATGC[A/G]TGACAAAAAATGCAT | 55130 |
| rs540434498 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27827137 | TGAAAATAACACTTT[C/T]CTGATTGTTTGTTAG | 55130 |
| rs540447805 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27836487 | TAAATTATACTAATA[G/T]GTAAACATATCTATA | 55130 |
| rs540456830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27857808 | TTACTTATGAATAGG[C/T]GACACGGTGACTCTG | 55130 |
| rs540458332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27850136 | AGTTTCCTCGTCTGC[A/G]AACTGTGTGTTTAAA | 55130 |
| rs540470940 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27970021 | TGAAGCAAGAGAATC[C/G]CTTGAACCTGGGAGG | 55130 |
| rs540481352 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27965285 | GGAGATTTCTGCCTA[C/T]GGTCCCCATGCCCTG | 55130 |
| rs540495121 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27938919 | TGTATCTTTTTGGCA[C/T]ACTCTCTTGATGCTG | 55130 |
| rs540500147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27957693 | AAGAATTTATACATA[C/T]ATAAAACTTGCAGGT | 55130 |
| rs540521760 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27943393 | TTTTTTTAAAGATGG[C/T]AGGTACATCTTTAAA | 55130 |
| rs540559682 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27919956 | CCCGTAATTTAGAAC[A/T]AAATGTCAGATAAAA | 55130 |
| rs540596406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27823764 | CATTGAAAATTAATA[C/T]ATTAACATAAGGTTC | 55130 |
| rs540618903 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27916152 | ATGTGGGGACAGAGA[C/T]TGAAAAGTGTGAAAG | 55130 |
| rs540626741 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27965679 | ATGTATCTGGGTCCC[C/T]AGTAATCCATAAAAG | 55130 |
| rs540634183 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27937095 | GAATGGATAGCAGTT[G/T]CTAAGTACTCAGCAA | 55130 |
| rs540671437 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27854923 | CAAAAAAACCAAGTA[C/T]TTACTGTAGGAACCC | 55130 |
| rs540689297 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27853487 | AGCTATAAAACTTTA[A/G]TATGCTAATATTAGT | 55130 |
| rs540705692 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27855387 | TATTACTCTATATGT[A/C]GTATATATTCATCGA | 55130 |
| rs540712680 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27823862 | AAAAATAGTTCAGGC[C/T]GGGCGCGGTGGCTCA | 55130 |
| rs540725452 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27908570 | GAAAGGTATATTAAA[C/G]TCAAAGCAGATGAAA | 55130 |
| rs540739073 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27884100 | TTTATGTAGAATATA[C/G]TCAAAGAGATCCCCA | 55130 |
| rs540740939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27956655 | AACCAACCATGTTCT[C/T]GGCATTATTCTAGTC | 55130 |
| rs540741901 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27862268 | AATACGCTTTCACAT[A/G]TATTAGTCTCAGAGA | 55130 |
| rs540749916 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27955788 | CTGAGCCCCACAAAT[G/T]CAGTCTTTAACAAAG | 55130 |
| rs540779327 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27915471 | CATTAATTTCATTTA[G/T]GAGGCCTCTACCCTC | 55130 |
| rs540794717 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27861141 | AGATTACAGGTGCCC[A/G]CCACCACACCTGGCT | 55130 |
| rs540828960 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27931162 | AGGTTGACTATGCTT[C/T]GAATGACCATGACAC | 55130 |
| rs540832204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27829246 | CAATTTTTCTTCTTC[A/G]ATGTCAAATAAATAG | 55130 |
| rs540836730 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27923077 | ACAAATTAAAGAGCA[A/T]GCAATAACAAAGAAC | 55130 |
| rs540846661 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27914684 | AATATGTATGTATGT[C/G]TGTGTATATATATAT | 55130 |
| rs540908496 | in-del | -/TATGTGTGTGTATATATA | 0.0437281 | 0.141251 | intron-variant | ARMC4 | GRCh38.p7 | 10:27914679 | TTATAAATATGTATG[-/TATGTGTGTGTATATATA]TATGTGTGTGTATAT | 55130 |
| rs540909448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27962353 | TCAAGTGCTCAATGG[C/T]CCACGTGCCTCGTGG | 55130 |
| rs540912682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27882260 | CTCTGATCTCATTCT[C/T]AATAAGATTTACTGA | 55130 |
| rs540915067 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27936376 | AAAAGAACAAAATCA[C/G]TTCCATCTCTAAAGA | 55130 |
| rs540949889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27891259 | ACCCAAGCATGTATC[C/T]CAACCTCACAGAAAT | 55130 |
| rs540964742 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27923668 | AATCCCAAGCACTGA[C/T]AGGGTACAGTGGCTC | 55130 |
| rs540966797 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27828623 | ATATGGTTATGTTCA[C/T]AATTTAACAAGGAAA | 55130 |
| rs540987126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27881481 | ACAAAAAAAAAAAAA[C/T]TAAAAATTAACTGGG | 55130 |
| rs541021251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27856183 | TGTAATGATACAAAT[C/T]CCTGGGCTGATACAT | 55130 |
| rs541023730 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27889819 | AGATTGGTGATCTCA[C/T]GTTGATAATAATGGT | 55130 |
| rs541024907 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27990854 | AATATATTTTTATCT[A/C]GATGCATATATATCA | 55130 |
| rs541027558 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27867841 | GTAATCCCAGCTATT[A/T]GGGAGGCTGAGGCAT | 55130 |
| rs541034256 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | ARMC4 | GRCh38.p7 | 10:27920805 | GTATACAAACAAGCA[G/T]AGCTTTACTTTTTTT | 55130 |
| rs541038566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27928816 | TAGCCTACATTTACA[C/T]ACAGCACTTATTATA | 55130 |
| rs541040117 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27935365 | AGATATTATTAAATC[C/G]CCATTACTGGATGGT | 55130 |
| rs541050307 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27970295 | ACTTTATATAGGTCC[A/C]TTCATATTTTTGAGA | 55130 |
| rs541053791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27903525 | GTCTTTGTTTGCAGA[C/T]GGCATGATTGTATAT | 55130 |
| rs541058085 | snp | C/T | 1.7187e-05 | 0.00293142 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983800 | TCTACAGCTAACAAT[C/T]AAAGTCCACTGGCTT | 55130 |
| rs541063854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27991589 | AATATAAATATATTG[C/T]CATCAATGTCCACAG | 55130 |
| rs541088260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997804 | GACCAGTTGCTCCCC[A/G]GTTTCTGCCCATTGC | 55130 |
| rs541088705 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27887958 | ATAGACAAATTTCTA[G/T]AAACAAACAACCTAC | 55130 |
| rs541094862 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27854818 | ATAATTTCATACAAC[A/G]GACTACCACTCAGAG | 55130 |
| rs541135386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27869366 | AGAATAAAAAAATCT[C/T]TCTCCTGAAATAAAT | 55130 |
| rs541138084 | in-del | -/AA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27975773 | TCTTCCAAAAAATTG[-/AA]GAGAAGATGAAACTT | 55130 |
| rs541158955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27896505 | AAGCAGGCCATGCGT[C/T]TGTTGCCTGGATAAA | 55130 |
| rs541166553 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27841128 | AATTATTAAGCCTAA[C/T]ATTCTAATATTGGAT | 55130 |
| rs541215568 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27938844 | ACCTGAAGTGATTCG[C/T]CCATCTCAGCCTCCC | 55130 |
| rs541218149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27813941 | AACTCTTCAATAAAT[A/G]GCCCCAGAACAACTG | 55130 |
| rs541264578 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27988809 | TTCACATCTGAATCC[C/T]CAAAACCTATGAACA | 55130 |
| rs541274345 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27868730 | ACTAAGGCATGCAGG[G/T]CTTAATACCTAGGTG | 55130 |
| rs541274687 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27858998 | AACTAACTGACAATT[C/G]TCTAAGCATATGCTA | 55130 |
| rs541293065 | in-del | -/TA | 0.0111196 | 0.0737302 | intron-variant | ARMC4 | GRCh38.p7 | 10:27885761 | ATATAATATATATTT[-/TA]TATATATTATATAAA | 55130 |
| rs541297854 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27968878 | TCAGTAGCCCACTGC[A/G]TGAGGGTGGCTTTAG | 55130 |
| rs541307928 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27851653 | AAAGAACAAAGTAAA[C/G]AAAGTCTCAGGGAGC | 55130 |
| rs541316098 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27874749 | TGATGGGCTTCCCTT[G/T]GTGTGTAACCCGAAC | 55130 |
| rs541322624 | snp | C/T | 1.69905e-05 | 0.00291461 | intron-variant | ARMC4 | GRCh38.p7 | 10:27961522 | ACATCTTTGGGAAAG[C/T]ATTTTAAATGAACAT | 55130 |
| rs541350855 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27848470 | CCTAGAGGAAAACCT[A/G]GGCAATACCATTCAG | 55130 |
| rs541351131 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27973256 | ATACATACATACATA[C/T]GCTGAGACAGCCAGA | 55130 |
| rs541352956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27874114 | ACCATTATGTAATGG[C/T]CTTCTTTGTCTCTTT | 55130 |
| rs541369709 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27832027 | TCGGGGCTTCCCCTG[A/G]AGGCTGGACCACATA | 55130 |
| rs541392139 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27936996 | TAGAGAGATCATTTT[C/T]GAAAGATGCCTCCAA | 55130 |
| rs541392778 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27834604 | GGGGGCAAGGAGTGA[C/G]ATAACGATGGAGAGG | 55130 |
| rs541431383 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27841681 | GATTACAGGTATGAG[C/T]CACCACCCCGGCAGA | 55130 |
| rs541458966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27848202 | GTAACCAAAACTGCA[C/T]GGTACTGGTACCAAA | 55130 |
| rs541472505 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27947416 | GCTGCAGTGAGCTAT[A/G]ATCACACTACCACTC | 55130 |
| rs541483692 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27967562 | GCAACACATACCTCA[A/T]CCTGCCAATATGGTG | 55130 |
| rs541487455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27849406 | GGGGCCTGTCGTGGG[A/G]TGGGAGGAGGGGGAG | 55130 |
| rs541488580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27982344 | TCATTTTTTTAAAAC[C/T]TAAAGGGATACTTAG | 55130 |
| rs541497885 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27847606 | GAAATAAAGGGTATT[C/T]AATTAGGAAAAGAGG | 55130 |
| rs541511290 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27941454 | CACACCACTGCACTC[C/T]AGCCTGGGCAACAAA | 55130 |
| rs541524048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27903563 | ACCCATCGTCTCAGC[C/T]GAAAATCTCCTTAAG | 55130 |
| rs541528059 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27856266 | ATCACACTGTATTGG[A/T]GGGGATTGATTAACA | 55130 |
| rs541535227 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27973796 | TTCTCTGGGTATATA[C/T]CCAGTAATGAAGTTG | 55130 |
| rs541547111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27974672 | TAGTGTGATACCTCC[A/G]GCTTCGGTCTGTTTT | 55130 |
| rs541547523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27934824 | CCAACTTAGCCCTCC[A/G]TCTCATATGAGGTAA | 55130 |
| rs541596358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27815710 | CCAAACAAAAATTGT[C/T]AGAGTTCATCAGAAC | 55130 |
| rs541614848 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27915256 | TCAGGCTGCAATAAC[A/C]GAATGCCATATGCTG | 55130 |
| rs541642460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27847285 | TACGCAAATCAATAA[A/G]CGTAATCCAGCATAT | 55130 |
| rs541646292 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27989393 | GACTTGCCAATGACA[G/T]GCATTGTTCACAAAA | 55130 |
| rs541649714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27909200 | AATAATGGCCTGCCC[C/T]ATCTTCTTGAAAATT | 55130 |
| rs541669008 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27822184 | GAAGGTGTGACAAAG[A/G]TAGCATGGGAATTGG | 55130 |
| rs541700427 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27813542 | ATAATCCTGGTAAAA[G/T]ATTTTTTAAAAGTAA | 55130 |
| rs541722648 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27867638 | CTTCTAAAAGACCAG[A/G]AAAACTCATTTCACT | 55130 |
| rs541737377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27820441 | TCAAGCATATGAGTC[A/G]TAATGTTTGGCATAC | 55130 |
| rs541755614 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27861455 | GTCTACTACACAACG[C/T]AAAATTACAGATCAG | 55130 |
| rs541762406 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27954440 | AGATGGGTATGTGTA[C/T]CATATCATGCTCTAG | 55130 |
| rs541769229 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27817091 | AGATGTATGCATGCA[C/T]GCATACACACTTTTA | 55130 |
| rs541775859 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944089 | ATTCTTAAGGGCAAG[A/C]GATACAGACAGAAGG | 55130 |
| rs541776223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27819920 | TGCATTTTTAGATCA[A/G]GACTGGACCAAGAGG | 55130 |
| rs541803658 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27848795 | AGCCAATAGACACAC[A/G]AGAAAATGCTCATCA | 55130 |
| rs541809283 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27892328 | TTTTATGACTAGTTC[A/C]CTTTAGTTTGACCTT | 55130 |
| rs541829541 | snp | G/T | | | missense | ARMC4 | GRCh38.p7 | 10:27994977 | TGTTCCATTCAAGTG[G/T]TTCCACAAAAACAAA | 55130 |
| rs541836427 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27929713 | ATGTGAAATTCTCAG[A/G]CAATATTTTTTCTCT | 55130 |
| rs541843427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27977336 | TTGAGAGGCCAAGGT[C/T]GGCAGATCACAAGGT | 55130 |
| rs541880578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27985419 | ACGAGATGCTCTAGT[C/T]TGTATTGTAACATCA | 55130 |
| rs541889895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983716 | GCAAGCATATATCAA[A/G]GGAATCTGCTTCTAT | 55130 |
| rs541891086 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27992858 | AGCACAAAATTTGTA[C/T]AAAGGCAAAACAATC | 55130 |
| rs541910307 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27891042 | TTATAGCAATATTCC[C/T]AGCATGAAACTAAAC | 55130 |
| rs541931050 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27932474 | TAATAGTCACAGAAA[A/G]ATTAAAAGATGATTT | 55130 |
| rs541952075 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27863182 | TATAGCTCATGCAAT[A/G]GAGCTTATTTAACAC | 55130 |
| rs541965136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27976431 | ATATAAAATCAGCAT[A/G]CAAAAATCAAGTGTA | 55130 |
| rs542005526 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27956483 | CAGATATCCAACTGT[G/T]CTTGCCAATATAACC | 55130 |
| rs542012654 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27990006 | TGGGAAGATCAGGAA[C/G]AATGAGCTATCAAAA | 55130 |
| rs542017334 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27846881 | TAAACCAGGAAGAAG[C/T]TGAATCCCTCAATAG | 55130 |
| rs542047011 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27848250 | TGAAAGAGAACAGAG[A/C]CCTCAGAAATAATAC | 55130 |
| rs542057043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27902485 | AGACAGGAAAAACTC[C/T]TCAAAAAATCAATGA | 55130 |
| rs542081802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27861454 | AGTCTACTACACAAC[A/G]CAAAATTACAGATCA | 55130 |
| rs542089225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27862373 | AAATGCATTGTTTTC[A/G]TCACTACACCATGAT | 55130 |
| rs542118211 | snp | A/G | 3.31499e-05 | 0.0040711 | intron-variant | ARMC4 | GRCh38.p7 | 10:27907783 | ATCAATTATCCTATC[A/G]TGGAACCCAAAATCA | 55130 |
| rs542121743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27869528 | AGTCACTTTTTTTTC[C/T]TTTTTCTTTTTCTTT | 55130 |
| rs542131370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27955936 | GATGTGAATGTCTTT[C/T]AGATGTCACTCTGGA | 55130 |
| rs542158043 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27874859 | CTTTTCGAGGAGTAT[A/C]TTTGTGGTGTTCTCT | 55130 |
| rs542168953 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27963030 | TTTTTTTTTTTTAGA[C/T]GAGATCTCGCTCTGT | 55130 |
| rs542173677 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27917533 | AAATAAAGGCAGATA[C/T]TAATGAAACAGGGAA | 55130 |
| rs542174763 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27951370 | TATACCAATGCTGTA[A/G]TAATTAAAACAGCAT | 55130 |
| rs542186721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27921576 | TTCCTGACAACTCAT[A/G]TATCTATATGCATAT | 55130 |
| rs542231801 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27835850 | AGAATCACTTGAACC[C/T]GGGAGGCAGGGGTGG | 55130 |
| rs542234328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27996487 | TTTAGTGTTGAGGAC[C/T]GACAATGTAAAATAT | 55130 |
| rs542259925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27828369 | AGAAGTGAGAGGGAA[C/T]AGTCAGTGTCAGAAC | 55130 |
| rs542268395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27843390 | GGTGTAGTGTACCAC[C/T]CAGCATAACTGGGTA | 55130 |
| rs542268459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27835211 | CTTCTTGGCCCTGAG[A/G]AGATGGGCTGCTGAA | 55130 |
| rs542279633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27975391 | ATCTATAGTCCTATA[A/G]GTGGATCAAAACAAA | 55130 |
| rs542289707 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27867699 | TCACGCCTGTAATCT[A/C]AGCACTTTGGAAGGC | 55130 |
| rs542295855 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27967392 | ACGAAGGACTCCCCC[G/T]TCACACTGTCCGGCT | 55130 |
| rs542297672 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27960190 | CATATTTTTCATTTT[G/T]CATTGATGTTGGTAA | 55130 |
| rs542300144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27881598 | GCTATAATCACACCA[C/T]TGCACTCCAACCTGG | 55130 |
| rs542305096 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27842399 | TTTTCTGGATAGACA[A/C]TAAGCATACATGATC | 55130 |
| rs542376143 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27880378 | CTTATGTCTAAAAAA[A/T]TTCCTTTGGGAGGCA | 55130 |
| rs542379071 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27901897 | TCAGTATTAGATCAA[C/T]GAGACAGAAAATTAA | 55130 |
| rs542435369 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27847851 | ATAAAATACCTAGGG[A/T]TCCAACTTACAAGGG | 55130 |
| rs542438620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27840849 | GTTATGAAGTAATTT[A/G]TTGATTTATAGCAGA | 55130 |
| rs542443356 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27983091 | CCCCAGCAACGGCCC[G/T]TCTTTCCACACAGTG | 55130 |
| rs542474069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27853995 | TTTGCAAATTACACA[C/T]ATGGTAAGCAACCAG | 55130 |
| rs542475542 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27839826 | TTAAAATGGTGAAGG[A/T]GCGTATCTTTTCTTA | 55130 |
| rs542507049 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27974524 | GTCAGCTTTGCTGTA[G/T]ATCAGATGGTTGTAG | 55130 |
| rs542561214 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27823874 | GGCCGGGCGCGGTGG[C/T]TCACGCCTGTAATCC | 55130 |
| rs542562151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27900289 | CAACAAAAAGGACGT[C/T]CACAAAAAATCCCCA | 55130 |
| rs542567930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27954539 | TGAATGAGTTGAAGC[C/T]TAAGGGAACTCCCCT | 55130 |
| rs542568550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27814067 | GTTCGACTAAAGACA[A/G]GGTCCTTGTCACAAG | 55130 |
| rs542570314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27941490 | ATCCTGCCCCCCGAA[C/T]CAAAAAAAAGAAAAA | 55130 |
| rs542600739 | snp | A/C | 0.100588 | 0.200439 | intron-variant | ARMC4 | GRCh38.p7 | 10:27846795 | AGAATACTATAAACA[A/C]CTCCACACAAATAAA | 55130 |
| rs542610381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27820534 | TCTCCTGTGTGTTCA[C/T]AAGACTTACGTTAGA | 55130 |
| rs542617133 | snp | A/G | 6.59294e-05 | 0.00574111 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27940608 | CACTGGAATTAGCAT[A/G]TTTTCATGAGAAGTC | 55130 |
| rs542635034 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27889675 | TTTCACACATGGACA[C/G]TCCCATGGACTTCAA | 55130 |
| rs542644702 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27853091 | AAGTAAGCCCTGGCC[G/T]GGCGCAGTGGCTCAC | 55130 |
| rs542659116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27933336 | AGCAAAGAAGTTAAA[C/T]GGGGCCATAAGACAA | 55130 |
| rs542665137 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27854121 | TGATATACAAGCACA[C/T]AGGATGTCCACATCA | 55130 |
| rs542704930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27812684 | CATTAATCTAAAGAC[A/G]TAAAGTTAGGCTAGG | 55130 |
| rs542717336 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27998478 | GGAGAAAGACGGGCT[C/G]GGGGAAGGAGAGGCA | 55130 |
| rs542718537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27861696 | ATTTTTTGATGCAGA[C/T]GATATCCTTCTTTGT | 55130 |
| rs542719892 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27873152 | TTGTGTGGAGGTGTT[C/T]ATAGTATTCTCTGAT | 55130 |
| rs542739498 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27818993 | TAACCCAACCTTCTC[A/T]TATGTGTAAAGGGAT | 55130 |
| rs542755130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27858794 | ACCATTACATGTACA[C/T]CTTAGTACATTTTTT | 55130 |
| rs542756354 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27827381 | ACACACACACACACT[A/C]TATATATATATATAT | 55130 |
| rs542758712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27879530 | GAAAAGTAATTCCCT[A/G]TTCAGGTTCAGACAG | 55130 |
| rs542785430 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27926958 | GAAAATTCAGCACAC[A/G]TAAATCTACTGTTTC | 55130 |
| rs542790354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27920477 | TGGAAAAATAAAACC[C/T]ACATAATCTTCAAAT | 55130 |
| rs542792264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27913117 | AAAATTATCATATAG[C/T]AAATATGTTTCTCCT | 55130 |
| rs542793457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27833890 | GCAAATCTGAAACCT[A/G]AAAGATGGTTATGAA | 55130 |
| rs542837753 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27911790 | TTGCCTTGTAGTCTT[C/G]TGTTGTGTGCTTCTT | 55130 |
| rs542850615 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27964258 | AACAAAACTCCATGG[C/T]TAGTGAAGTGGCTGT | 55130 |
| rs542877228 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27981263 | GATATTTGTACAACA[C/T]TGTGAATGTAATTAA | 55130 |
| rs542877554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27905545 | TGGAACCAAAAAAGA[A/G]CCTGTATAGCCAAGA | 55130 |
| rs542914081 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27973793 | TATTTCTCTGGGTAT[A/C]TACCCAGTAATGAAG | 55130 |
| rs542948355 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27879569 | AAACAGTGAGTTGTA[C/T]GGATTAGGCTAAGAA | 55130 |
| rs542962467 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27918291 | ATCAGCAACATGAAC[G/T]CAAGAATGCATGAAA | 55130 |
| rs542970191 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27887539 | CTCATTTTTCTCAAG[C/T]GTACAATAAACGTTC | 55130 |
| rs543009416 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27854704 | GAGGTTGCAGTGAGC[A/C]CAGATCGCGCCACTG | 55130 |
| rs543020571 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27963722 | TCATGTTTTTGATTA[C/T]AGGGTATTGGCTCAC | 55130 |
| rs543039691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27988065 | GAATTCCTTTCCCAC[C/T]CTAAACTTCTTTATT | 55130 |
| rs543039748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27995660 | TTACAGTGACAATAT[C/T]TGCATCATCACAATG | 55130 |
| rs543048088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27861576 | TCTCCACCCTAGGAA[C/T]ACATTGATATCAGTA | 55130 |
| rs543057415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27821330 | TACTCATTGCTTTGT[C/T]ATACACCCAGAGGGG | 55130 |
| rs543073376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27859327 | TACATGCCATAAAAA[C/T]AGATTTATAATGGAA | 55130 |
| rs543085188 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27860962 | GTCTAGAGAAAAGGG[A/C]TAGCTGGCTGACTAC | 55130 |
| rs543089299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27954687 | GCTTTTTCTCCACAC[A/G]TATTTATTTTTGACT | 55130 |
| rs543091181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27961451 | TAGATAAAACAACAG[A/G]AATGCTTACTACTCT | 55130 |
| rs543106656 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27914128 | AAATGTACATACAAA[A/C]CATGGAGTACTACAC | 55130 |
| rs543123261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27868674 | TAACACACATTGGGG[C/T]CTGCTGGGGCACGGA | 55130 |
| rs543138453 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27815465 | GCTGTCTGCCTTCAG[C/T]TCTCCTCTGAAATAA | 55130 |
| rs543161972 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27874654 | TCTGGGTTGAAAATT[A/C]TTTTCTTTAAGAATG | 55130 |
| rs543195300 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27828539 | GTTGAGGTATTTTCT[C/G]GCTTTTACTTCATTT | 55130 |
| rs543209210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27825267 | TTGAACTGAATTTAA[C/T]GATTAGGCCAAGTTC | 55130 |
| rs543211125 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:28000926 | TTTTTTCTTTTTTTT[C/T]TTTTTGAGACGAGGT | 55130 |
| rs543252935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27960853 | TCACAAATACTTCTG[A/G]ACGTCGGCTTTACAC | 55130 |
| rs543265298 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27994650 | TGTTGGCAGTGTAGT[C/G]ACCTGGATAACGGAT | 55130 |
| rs543265898 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27921323 | AAAGAAAAAAAAAAG[A/G]ACATGAAATTTAACT | 55130 |
| rs543278586 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27871215 | TTGTTTGTTTTTTTC[C/T]TCTAAATTTGTTTGA | 55130 |
| rs543282054 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27865838 | TGCAAGTGTGAGGGC[A/G]AAGCCACTTTCTCTC | 55130 |
| rs543285937 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872525 | ATTATTTTGAGATAC[A/G]TCCCATCAATACCTA | 55130 |
| rs543292640 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ARMC4 | GRCh38.p7 | 10:27968644 | GTTAAGAGCCCAGTG[C/T]TCCTAAACTTAGGTC | 55130 |
| rs543310831 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27841645 | AGGTGATCTGCCTGC[C/G]TCGGCCTCCCAAACT | 55130 |
| rs543316741 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27867979 | AAGCAGTATAAAAAA[G/T]ACTCCAGTCAATTTC | 55130 |
| rs543322980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27871993 | CTATCCAAGAGCATG[A/G]AATGTTCTTCCATTT | 55130 |
| rs543324946 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27964842 | ATTTCTGTCTTTTAT[A/C]CTGTCTCCCCTAGCA | 55130 |
| rs543338590 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27944110 | AGACAGAAGGCTCCT[A/G]GAACACGCTCTCATG | 55130 |
| rs543340084 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27868599 | GAAAACCAAACAACA[C/T]GTGTTCTCACTCATA | 55130 |
| rs543357386 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27948186 | ATCCTTATAGAAAAA[A/T]ATTCTGTAAATCATC | 55130 |
| rs543364938 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27965777 | CAGATGTTTAACTTG[C/G]ATTTACAAAAATTGA | 55130 |
| rs543406761 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27844171 | CTGTACTCCAACTTG[C/G]ACAACAGAGCAAGAC | 55130 |
| rs543416874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27814177 | AAACAGGGACCCTCC[A/G]CAAAGCCAGAGTCCC | 55130 |
| rs543420762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27990070 | AGAATCGTGGAAGGG[A/G]GCTAAAAATTCTGTT | 55130 |
| rs543452839 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27892231 | CTTAATAGGAAAAAA[G/T]AACTTTTCTTAGACA | 55130 |
| rs543482219 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27973900 | TTTACACCCACCAAC[A/C]GTGTGTACGTATTCC | 55130 |
| rs543485248 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27976201 | ATCAGGAACAAGAGA[A/C]CATTTCTATTCAATT | 55130 |
| rs543512311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27868207 | GTCTGTGGAGAAATA[A/G]GAATACTTGTACACT | 55130 |
| rs543549011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27820724 | TCATTCTATATCCCA[C/T]ATGCTGGTTGGTTAA | 55130 |
| rs543569986 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27921944 | GGCCAAGGAGGGTGG[A/T]TAGCTTCAGCTCAGG | 55130 |
| rs543579260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27812853 | TAGACTCCTTCCTCC[C/T]CACTTTCTCTGGGTA | 55130 |
| rs543599506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27912853 | TTAAAATGATCATCC[C/T]TGGGAAAAACAGATT | 55130 |
| rs543599622 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27906117 | TTGCAATCTATCAAT[A/C]TGACAAAGGGCTGAT | 55130 |
| rs543602813 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27946300 | CGTGGAAATTCCATA[C/T]CAGCTGCCAAACTCC | 55130 |
| rs543610176 | in-del | -/AGGG | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27998278 | AGACATGACATGAAC[-/AGGG]AGGGCCCTAAGTAAA | 55130 |
| rs543619718 | snp | A/T | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997640 | AGCAATGCACAAGTT[A/T]TATTCAAGAAGGTTG | 55130 |
| rs543628876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27819778 | GTTTGATAGTGATTT[C/T]TCTAGGAAGGAGTGA | 55130 |
| rs543636084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27906690 | ATGCAGCCATAAAAA[C/T]GAATGAGTTCATGTC | 55130 |
| rs543650577 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27874057 | GTATTGGGTGCATAT[A/C]TATTTAGGATAGTTA | 55130 |
| rs543665779 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27834373 | AGACATACAACCCGT[A/G]ACACCACAGGCATCC | 55130 |
| rs543670883 | in-del | -/AAAC | 0.0119091 | 0.0762411 | intron-variant | ARMC4 | GRCh38.p7 | 10:27859836 | CTGATGCACAGATTT[-/AAAC]AAACAAACAAACAAA | 55130 |
| rs543703437 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27967517 | CCTATGGGAAAACCT[C/G]CTATTTCAATTCCTC | 55130 |
| rs543760474 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27911120 | GCACTTAGGAACACT[A/G]GGCGGCACTTCAGCA | 55130 |
| rs543764641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27879696 | CCAAAAGTTTACTTG[C/T]TGGATCTGTTACATA | 55130 |
| rs543795855 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:28001037 | GCTCAAGTGATCCTC[C/T]AGCCATGGCCTCCGA | 55130 |
| rs543819619 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27978476 | ACTCAGGAGGGTCTA[C/T]AAAATGATGGGTGCA | 55130 |
| rs543819740 | in-del | -/T | 0.00762123 | 0.0612579 | intron-variant | ARMC4 | GRCh38.p7 | 10:27952861 | AGGAGCTATGAAACT[-/T]TTTTTTTACATAAAC | 55130 |
| rs543831402 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27981340 | GTTATGTTATGTTGT[A/T]AAAAAAAACCACTAA | 55130 |
| rs543843726 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27918391 | ATCATGGTGAGTCAC[C/T]TTATTAATAGAACAA | 55130 |
| rs543846803 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27825324 | ACTTTAAAGGTGCAG[A/C]CTAGCGAAAACAAAA | 55130 |
| rs543852784 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27923951 | CCTGTCTAATGAAAG[A/T]AAGAAAGAAAGAAAG | 55130 |
| rs543890466 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27887164 | TGAAAGTCAAACGTT[A/G]AAATAGGACATTCCA | 55130 |
| rs543896408 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27895978 | AAGAAGAAACAGCCT[G/T]GCAAATCAGGCCACT | 55130 |
| rs543905109 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27853158 | CAGATCACGAGGTCA[A/G]GAGATTGAGACCATC | 55130 |
| rs543918669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872073 | AAGAGTACCTTCACA[C/T]CCCTTGTAAGTTGGA | 55130 |
| rs543927517 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27911553 | GCGTGGAGTTTCACA[C/T]GAACACAGACAGAAG | 55130 |
| rs543937419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27972287 | TTTAGTAAGAAATAT[A/G]ACTAGTAAACCAATA | 55130 |
| rs543938594 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27852671 | ATGGTACATTTAAAG[C/G]TAACCGTGGCCGGGC | 55130 |
| rs543974201 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27965028 | TGGACAGGAGGCAAC[A/T]GTCAGTAAGACTGAA | 55130 |
| rs543995261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27953612 | AAATACTATGTAGTC[A/G]TTAAAAGGAGTGAGG | 55130 |
| rs544007380 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27819205 | TGGAGGAGCACAGGT[C/T]GGGGGAATTTACACT | 55130 |
| rs544070916 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27859361 | TTGACACATTCAAAC[A/G]TATATTGAGTTTAAT | 55130 |
| rs544074860 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27836067 | GAAGAGGAAGAGGGG[C/T]TGGTCTTGCTGTCTC | 55130 |
| rs544102783 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27838977 | GCCAGCATCATCTTA[C/T]GCCAATCTAACGCTT | 55130 |
| rs544105819 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27857829 | GGTGACTCTGGTCAT[A/T]GTTAAAGAGCCTGTC | 55130 |
| rs544106672 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27845339 | CTTCATAAGTGAAGG[A/G]GAAATAAAATCCTTT | 55130 |
| rs544110236 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872594 | TTGTCAAAGGCCTTT[C/T]CTGCATCCATTGAGA | 55130 |
| rs544142246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27899682 | TTTCCCCTCACAGTG[C/T]AAACAAAGCCTCCAG | 55130 |
| rs544144591 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27837027 | CCTAAACTGCCCACC[A/G]TGAGGATTTCTGGGA | 55130 |
| rs544144958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27850512 | TAGTGAGCTGATATC[A/G]TACTACTACACTCTA | 55130 |
| rs544149795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27959870 | CTGTAAAAAAACTTA[C/T]GTAATAAATGCATGA | 55130 |
| rs544151735 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27953026 | ATATAAAAAAATGCA[C/T]ATCTTTAATGTATAC | 55130 |
| rs544167624 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944643 | AGAAGAGCAAAAAAA[G/T]AAGAAAAGTAGAAAA | 55130 |
| rs544207866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27919002 | AATGGAAAATGTGCA[A/G]TGCTCTACATTGCAA | 55130 |
| rs544212470 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27832992 | AATATGGCTTTTCCA[A/C]CTTGGCAGGGGCAGG | 55130 |
| rs544219341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27823726 | TGTTGGACTGATCCA[A/G]ATAAGCAATTTTAAT | 55130 |
| rs544240084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27951520 | CAGATAGGCCAATAA[C/T]CTGTGTTGATACAAT | 55130 |
| rs544241629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27864754 | TATGGGGGTGAGTGT[A/G]ATGTCCACCAATTAC | 55130 |
| rs544243109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27965863 | CACTTTATTCCTCAT[C/T]GCTCTAGAAGTTTCT | 55130 |
| rs544246300 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27832499 | TTATCCACAAGCTCA[A/G]CTTTCCCCCCACCCA | 55130 |
| rs544260753 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999596 | CATTAAGATGGTTTT[G/T]ACCCCACCTCTAGAC | 55130 |
| rs544269082 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27904313 | GGATGCTGTGTATGC[A/G]CGGGGAACATGGCGT | 55130 |
| rs544284279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27838615 | AAAGCTAGATAAATA[C/T]AGAAACGAAATATAG | 55130 |
| rs544284941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27964091 | GCTGGGTATGGTGGC[A/G]TGTGCCTCTTGTCCC | 55130 |
| rs544298261 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27972988 | AAAAAATCACCAAAA[C/T]AGATCATATACTGGG | 55130 |
| rs544312712 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27908061 | ATTAGCTGTACACAG[A/G]CCTGTTACCTAAATG | 55130 |
| rs544346459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27831705 | CCTGGCCTCATTCTT[A/G]GATGCCTGGGGTTGG | 55130 |
| rs544385314 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27939161 | CACACACACACGCAT[G/T]CCTCTGGCTAGTCTT | 55130 |
| rs544393841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27870756 | ATCCACTCTATCATT[A/G]ATGGACATTTGGGTT | 55130 |
| rs544397550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27820235 | GCTGCCACCCTGTAC[A/G]GCTCTCTTGGAAAGG | 55130 |
| rs544414148 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983658 | TAATGACCTGCAGTG[A/G]AGAATAAGAGAGCTA | 55130 |
| rs544429193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27823867 | TAGTTCAGGCCGGGC[A/G]CGGTGGCTCACGCCT | 55130 |
| rs544451877 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27994506 | AGGCTGAGGCAGGAG[C/G]ATCACTTGAGGCCAG | 55130 |
| rs544459668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27923755 | GAGTTCAAGACCAGC[C/T]TGGACAACAGAGCAA | 55130 |
| rs544481259 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27905414 | CATGGATAGGAAGAA[A/T]CAATATCATGAAAAT | 55130 |
| rs544513884 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | ARMC4 | GRCh38.p7 | 10:27811946 | CAGATGTTTGCTAGT[A/G]TTTAGGAGAAATTTG | 55130 |
| rs544521707 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27945256 | GCTGACTGAGGAATG[A/C]AAGATGTACACAGAG | 55130 |
| rs544544742 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27938569 | AATACAATCCTCTAC[G/T]GAAATGACTCCCTTG | 55130 |
| rs544568378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27817917 | CAGATACAACTTTAT[A/G]AAATTTAGACGATTT | 55130 |
| rs544628489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27817465 | ATAGTGAACACTGCA[C/T]CCAATAGGTAATTTT | 55130 |
| rs544640421 | in-del | -/AAAC | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27910767 | TCTCAAAAAAACAAA[-/AAAC]AAACAAACAAACAAA | 55130 |
| rs544667423 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27909898 | ACATGATTGAAAAAC[A/G]TTTGCAACCATAGGA | 55130 |
| rs544667798 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27973700 | ACTGATGGCCATTTA[G/T]GTTGACTTGATGTTT | 55130 |
| rs544670632 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27871140 | GTGTGTCTATTGGCT[A/G]CATAAATGTCTTCCT | 55130 |
| rs544683477 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27849116 | ACGTATGTTTACTGC[A/G]TCACTGTTCACAATA | 55130 |
| rs544707606 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27877216 | TTTGCTCCTCTGGAG[A/T]TGACCTCACAGCGAC | 55130 |
| rs544725117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27878669 | ATCCTACACTAACAT[C/T]AGAATAGCATGTCAG | 55130 |
| rs544742882 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27876568 | AAACTCCCACTTAGC[C/G]CTGCAAACTCTAACT | 55130 |
| rs544747633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27824800 | CTGTCTGTATTCTGT[C/T]GTTAGATCCATTTTC | 55130 |
| rs544763604 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27916988 | GATAAAATAAAATTT[A/T]AAAAATGATAAAGAT | 55130 |
| rs544783994 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27959463 | CAGTAAAGATGCAGA[A/G]GCACTGTTGCAAGCG | 55130 |
| rs544831097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27973171 | ATAGTTTATACAATG[C/T]TCATAAAGAAATTTG | 55130 |
| rs544843364 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27942019 | GGATGGGGTATGGAG[A/G]CTTCCAGGTACTGAC | 55130 |
| rs544862018 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27845938 | CAAGTCCTTAGAGAC[C/T]TACAAAGAGACTTAG | 55130 |
| rs544907956 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27930019 | ACCAATTACGTTTAT[C/G]TTGGCTCTCCTTGGG | 55130 |
| rs544916316 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27947061 | AGCCTTAATTTTACT[A/G]TTTACTAATAAGTCA | 55130 |
| rs544947646 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27883370 | AGTTAATAACAAAAT[A/C]AACAATAGCAAAAGC | 55130 |
| rs544961562 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27945277 | GTACACAGAGCTAAG[A/T]GATGGTTCCCCCAGT | 55130 |
| rs544986635 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27827210 | CCCTTTCTTAACCCA[G/T]TATGATATGACTCAG | 55130 |
| rs544989200 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27918032 | TAATTTTAAAAACCA[A/G]TTAAAAAGGAATCCT | 55130 |
| rs544996490 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27851132 | GAAGGAATAATCTTC[C/T]AAACTCCTGCAAGGG | 55130 |
| rs545007376 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27894831 | TTGGCCTCTCAAGTT[C/T]TGGGGTCACAGGTGT | 55130 |
| rs545028793 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27826377 | TTCCATCGGCTCTCC[A/G]TGTTGCCCGGTCATC | 55130 |
| rs545049652 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27994625 | AGGCCAGGCATAAAG[C/G]AGCAATGGATGTTGG | 55130 |
| rs545087412 | snp | G/T | 3.30033e-05 | 0.00406209 | missense | ARMC4 | GRCh38.p7 | 10:27987425 | TCAACTTCCCAGTTT[G/T]GGCAATAAGTAACAA | 55130 |
| rs545092476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27966356 | AGTTCTTTGAGGAAA[A/G]CCTAAATTCACCTTC | 55130 |
| rs545138294 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27833401 | AATCAAGGAGGAAAA[C/T]TAAACTTCTCTAGCA | 55130 |
| rs545144333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27825213 | AATCTGTCCTGACAT[C/T]TTCCCATTACCATCA | 55130 |
| rs545145769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27887435 | AACTAGAGAGAACAT[A/G]AATAAGGAAATAGAA | 55130 |
| rs545164835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27824627 | AGCAAAGACATGAAT[C/T]AAATTATCTAGAACG | 55130 |
| rs545166659 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27839683 | GGTTTAAACATAAAG[C/T]TGGGAGCCAACAGCG | 55130 |
| rs545189500 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27884501 | TTCCTTCCTTCAGCC[A/G]GAAGGACCAAAGTGG | 55130 |
| rs545195245 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27859537 | ATATGACTAACTGGG[G/T]TTTTTAACTCTTTGC | 55130 |
| rs545239894 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27920970 | TATCCTTGTGTATGT[A/G]AAAGAGTCTTTCATT | 55130 |
| rs545323015 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27854866 | GCCACATAAGAATGT[C/G]AATTAATACGAAAAT | 55130 |
| rs545337198 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27831353 | CACCGTTATAGACCC[A/T]GGAAAGGCAGAGGGG | 55130 |
| rs545340570 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27879610 | AACCATAATTACAAG[A/G]AAAAAATCTAACTAT | 55130 |
| rs545359081 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | ARMC4 | GRCh38.p7 | 10:27812024 | TTCTATTTAATAACA[C/G]TTTGTGAAATCAGCA | 55130 |
| rs545365935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27931355 | TTGCTCTCTTTTTGT[A/G]GGTTTCATGCCATTA | 55130 |
| rs545383361 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27964344 | GGTAGTCTTTTAACT[A/T]ACGTGTGCCTCGGTT | 55130 |
| rs545394877 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27818587 | CCTATACTAAGAGCT[G/T]GATTTCCATACGCAA | 55130 |
| rs545398963 | snp | A/G | 3.30759e-05 | 0.00406655 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27995121 | CAGTCCACTGCGTCA[A/G]TTTCCTCAGAGCCAC | 55130 |
| rs545401261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27816373 | GGGAAACAGGGAAGT[C/T]TGGAGGGGCTCATGC | 55130 |
| rs545405584 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27931820 | CAGAATAGAAGTAGA[C/G]GCTTCGCAAGAGTAA | 55130 |
| rs545405735 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27923924 | ACTGCATTCCAGGTG[A/G]TAGAGAGAGACCCTG | 55130 |
| rs545406285 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27897689 | AAATGTTCGTGTTGC[C/T]GCAATGATAAATGCA | 55130 |
| rs545417361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27858680 | TTGGTCACTTTACAC[A/G]GTAGGATAATATTCA | 55130 |
| rs545461293 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27958370 | TAGGCTATTATGAGA[A/C]ACTCTCTTTGCCATG | 55130 |
| rs545476517 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27904729 | TCCCTGGCTATTCCG[A/T]CATGTTTATTTTCCA | 55130 |
| rs545502082 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27844802 | TAGCTTTTCTTTTTC[A/C]TTTCTTCTCACTTGT | 55130 |
| rs545529929 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27871948 | AAATTACCTTGGGCA[A/G]TATGGCCATTTTCAC | 55130 |
| rs545535509 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27818588 | CTATACTAAGAGCTT[C/G]ATTTCCATACGCAAA | 55130 |
| rs545556380 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:28000114 | GCGCCGCCATGCCCG[C/G]CTAATTTTTGTACTT | 55130 |
| rs545570252 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, intron-variant | ARMC4 | GRCh38.p7 | 10:27998817 | CCTGCAGCACCCTGC[C/T]CCCCGCAGTCGGCGC | 55130 |
| rs545616743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27937477 | CCAATCAAGTTTCTA[C/T]GCCCAGAGCAGTGAG | 55130 |
| rs545622138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27964784 | AATTTTTATTTCTGC[A/G]TTTTCTTGTAGTGTC | 55130 |
| rs545642191 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999643 | CCCCAACTGGAACAC[A/C]AGTGAGGGATAAAGG | 55130 |
| rs545649034 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27828398 | ACTTCCAGCTTCTGG[A/T]GAAGTCAAAATGAGA | 55130 |
| rs545654740 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | ARMC4 | GRCh38.p7 | 10:27928346 | ATAGGTCTTTATTTA[A/T]CCTATCGATTTCTCT | 55130 |
| rs545685151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27971460 | AAACAAGGACAACAT[C/T]AAGACTAAGGCTTCT | 55130 |
| rs545694366 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27992324 | GTAAATATGACAGAA[A/G]TATAAAAATCAAGGG | 55130 |
| rs545699306 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27877303 | TGGGGCCATACTGGG[A/G]AAAATGACAAAAGTG | 55130 |
| rs545705815 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27884992 | CTGTTTCTTTAAATG[C/T]CCAGTTTTCAACAGA | 55130 |
| rs545709984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27889223 | CCTAGAGAGATCAAG[C/T]TGGACCCAACCTTCT | 55130 |
| rs545728304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27837826 | CATAAGGATAAGCCA[C/T]TGTGGTCCATCACTC | 55130 |
| rs545731355 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27998281 | ACATGACATGAACAG[C/G]GCCCTAAGTAAAACC | 55130 |
| rs545749509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27863304 | AGTGAAATAACCAAC[A/G]AAAAGCACAAAAATC | 55130 |
| rs545755950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27957055 | GAGCCTAGAGACATT[A/G]ACAAACCATCTCCTT | 55130 |
| rs545765447 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27845113 | AAGACACATAATTGT[C/G]AGATTCACCAAAGTT | 55130 |
| rs545806949 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27874371 | TTTAAGGTTAATATT[A/G]TTATGTGTGATTTGA | 55130 |
| rs545844276 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27970860 | GCCTGTAATCCCAGC[C/T]ACTCAGGAGGCTGAG | 55130 |
| rs545860761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27977170 | TTCATCATTATACTG[A/G]GTTTGGAAAAGCGTT | 55130 |
| rs545870250 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27979572 | TGTATTTCTATACAC[C/T]AGCAGTGAATAATTG | 55130 |
| rs545879263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27875475 | TCTGTTTTTCCCCAT[C/T]TTTGTGGTTTTATCT | 55130 |
| rs545913546 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27963376 | CAGGCTCTATTATCC[A/C]CATTCTACAAGCAAG | 55130 |
| rs545950407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27817333 | CACTTTACTGTATAG[A/G]CAGTTAAAATTCTTT | 55130 |
| rs545954748 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27991655 | CAGAATTTCAGCGTA[C/G]ATAAAACTTAACTTG | 55130 |
| rs545980016 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983775 | GTCATTGGGACACAC[C/G]CTTGAGACATCTACA | 55130 |
| rs545981183 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27933016 | ATCTCAGTACTTTGG[C/G]AGGCTGAGGCAGAAG | 55130 |
| rs545982583 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27969932 | CCAACATGGCAAAAC[A/G]CCATCTCTACTAAAA | 55130 |
| rs546018787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27976561 | ATAAGACCTGTATAT[C/T]GAAAGCTACAAAACA | 55130 |
| rs546039333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983215 | TATCACTATCAGTCA[C/T]CCAGTGCTCCATTTT | 55130 |
| rs546039983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27891152 | AGGGTGATGTCAAAT[C/T]CCTGTCCTGTTTGAT | 55130 |
| rs546068677 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27975683 | GCCCAGATGGCTTTC[A/G]CCAAACATTTCTACC | 55130 |
| rs546111568 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27848683 | AGGGCTAATATCCAG[A/T]ATCTACAAAAAACTC | 55130 |
| rs546133416 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27949895 | ACTTGGTTCAGGAAA[G/T]GATGCTACAAGTGTA | 55130 |
| rs546134423 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27990761 | CAGAAAGGTATAAAT[G/T]GTGTGTGAATTGTGC | 55130 |
| rs546157292 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27914759 | TATATAAAATGGAAA[A/T]GCTATATTTGAAAAC | 55130 |
| rs546160476 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27916428 | CAAATAAGTAAGGAC[A/G]GAGGTCAGTTTCTCA | 55130 |
| rs546163255 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27822298 | TGAGTGATAACAGAT[C/T]TTCTTGTGGTTTGAC | 55130 |
| rs546166274 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27824109 | TTGCGCCACTGCACT[C/G]CAGCCTGGGCGACAG | 55130 |
| rs546196619 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27922810 | ACTATGGTGGCTGAG[A/G]CAGGAGAATCATTTG | 55130 |
| rs546200878 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27830676 | TATGTTATACTGACT[C/T]GTCTGAATATTCTCC | 55130 |
| rs546216973 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27923996 | AGAAAGAAAGAAAGA[A/G]AGAAAGAAAGAAAGA | 55130 |
| rs546228337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27869561 | TTTTTTTGAGATGGA[A/G]TTTCACTCTTTTGCC | 55130 |
| rs546242519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27969370 | CAACGTTGCAACAGG[A/G]CCTGCACCTGGTTTT | 55130 |
| rs546261308 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27825455 | CTTTAGAAATGGCCA[C/T]GAGTCTTTTTAAGAA | 55130 |
| rs546289143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27910246 | ATATTCATTCTGTTC[A/G]TGACACTAGCTAGCA | 55130 |
| rs546322912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27923944 | GAGAGACCCTGTCTA[A/G]TGAAAGAAAGAAAGA | 55130 |
| rs546335508 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27926335 | CGGGATATAGAATTA[C/T]CATACAGAATTCAAC | 55130 |
| rs546340076 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27831090 | GGCATGAGGAGGGAT[A/C]TGGAGGCCAACGGCC | 55130 |
| rs546355336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27893147 | CTGGGCGACAGAGCC[A/G]GACTCCTTCTCAAAA | 55130 |
| rs546360037 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27930540 | AACAGGCTGAGAGAA[C/T]GGCGTGAACCCGGGA | 55130 |
| rs546363704 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27949653 | GCTGCTGGGCCCAGA[A/G]TCTGGGCTGAGAATT | 55130 |
| rs546394167 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27923384 | TAGAAATCAAGCCAA[A/C]ACACATTAAACCTGA | 55130 |
| rs546395987 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27842563 | TACCATTTGAAAGAT[C/T]AATTTATTAAACAGA | 55130 |
| rs546421570 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27929798 | TACAGCCAATGGTTT[C/G]CTTCTTTTGCCTGGA | 55130 |
| rs546423551 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27840508 | ACATGCTTCATTGTC[C/T]ACCACTGATTGGACA | 55130 |
| rs546448691 | in-del | -/AAAG | 0.00360648 | 0.0423111 | intron-variant | ARMC4 | GRCh38.p7 | 10:27931128 | CTCTTAAAAAAAAAG[-/AAAG]AAAGAAAGAAAGAAA | 55130 |
| rs546471251 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27977465 | CCAGCTACTTGGGAA[C/G]CTGAGGCAGGAGAAC | 55130 |
| rs546473435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27890238 | CTGGAAGAAGAGGCC[A/G]TCTGGGGTCCCAGTC | 55130 |
| rs546475729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27942091 | GGATTGAACACAGAT[A/G]CACAACAATAAATGA | 55130 |
| rs546477224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27836959 | AATCAGGATTTTCCC[C/T]GGCTTTGCAGGGAAT | 55130 |
| rs546480589 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27950168 | TTTTTTCCTTCAAAC[A/G]TGCCACTCAGAGAGC | 55130 |
| rs546487658 | in-del | -/ATAAGG | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27837812 | CCTGACTTGTCAACC[-/ATAAGG]ATAAGCCATTGTGGT | 55130 |
| rs546522283 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27959670 | AAGATTCAGGAATAT[A/G]CAATCAAAATTCCTA | 55130 |
| rs546575072 | in-del | -/GTT | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27955875 | AACCTGCCAGGGAGG[-/GTT]AGCTCTGGGAGTCCC | 55130 |
| rs546589850 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27831467 | ACTCAAAGTGCCTTA[A/T]AAGATACTGATTCAT | 55130 |
| rs546608064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27937136 | CCAGTTTTGAGATAG[C/T]CTAGGCATCTCCTGA | 55130 |
| rs546624941 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27837396 | GACGTTCTGGCAAGT[A/C]ATTTCCTAGGCAAGT | 55130 |
| rs546667791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27876836 | TCCCTGATGAACTTC[C/T]TGAGCTGCAGAATTG | 55130 |
| rs546704560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27884504 | CTTCCTTCAGCCGGA[A/G]GGACCAAAGTGGAAG | 55130 |
| rs546705800 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27870556 | TCCCCTTCCTGTGTC[C/T]AAGTGTTCTCATTGT | 55130 |
| rs546706620 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27885205 | TAAACAAAATGAGAA[C/T]ATAAACAAGGAGACA | 55130 |
| rs546736014 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997958 | ATAAACTGGGATGTT[A/T]ACATAAACTGGGAAT | 55130 |
| rs546745666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27875580 | TGGTTCCAAGATGGC[C/T]GAATAGGAACAGCTC | 55130 |
| rs546757598 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27887638 | AGTATCTCTTCTGAA[C/T]ACAATGGAATAAAAA | 55130 |
| rs546759472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27956093 | CAGTGTTTGATGAAT[C/T]TGATGATACAGAACA | 55130 |
| rs546760565 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27962349 | CATTTCAAGTGCTCA[A/T]TGGCCCACGTGCCTC | 55130 |
| rs546787603 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27993534 | GGATGCCTATATTCC[A/G]AGCTACTTAGGAGGC | 55130 |
| rs546805110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27844853 | AATTTATTTGGCTAG[C/T]GATGGGGTGGTGGCG | 55130 |
| rs546809934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27978028 | CTAGGCACATTGAAA[C/T]TATATGATCATACAA | 55130 |
| rs546828699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27908910 | TAAAAAGGACTTCTA[A/G]TAAGAAAAAATACAC | 55130 |
| rs546842104 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27844435 | GCAGAGTTTCTCAAC[C/G]AGGCTCAGTCCTTCA | 55130 |
| rs546854088 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27970301 | TATAGGTCCATTCAT[A/G]TTTTTGAGACTCTAG | 55130 |
| rs546859872 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27969098 | TGGCAATGTAGATAT[A/C]TACTCCGTTATTTCC | 55130 |
| rs546867018 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27936625 | GAATGTACATCTACA[A/G]CTAACATTAGAATTG | 55130 |
| rs546875232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27856558 | CCACCCTCATTAATG[A/G]CTTAATACCCCCTGC | 55130 |
| rs546896740 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27969426 | TCCTTGGCATTCTGT[A/G]TTCTCCCTTGAATAC | 55130 |
| rs546909819 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27919076 | CAATATATACCTCAT[C/T]AATGGATTGGCAGTC | 55130 |
| rs546924693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27962701 | GACTTCTGGAATCCA[A/G]TATATGCCCTACGTC | 55130 |
| rs546928912 | snp | A/C/G | 0.000527591 | 0.0162332 | synonymous-codon, missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27812578 | TATACAACCAGCTGC[A/C/G]GCTTCCTGGAGATCC | 55130 |
| rs546940230 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27936054 | CTTTTAATCTAGCCA[C/T]GACTTCACTACGCCT | 55130 |
| rs546972802 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27949948 | GCAACACGCTTGCAG[G/T]GTCATCATTTGAAGT | 55130 |
| rs546978229 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27842624 | ACATTCTATAAAGCC[A/G]TGGGCCATGTCCAGA | 55130 |
| rs546979126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27816834 | GCTCACTGCAACCTC[C/T]GTCCCCTGGGGTTCA | 55130 |
| rs546988826 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27974997 | TTTGTTCTTTTTGTG[A/C]TAATTGTGAATGGGA | 55130 |
| rs547011573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27863373 | TTGCTTACAGTATGA[A/G]AAATGAAACAAGAAG | 55130 |
| rs547015083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27841957 | AGATAGGGTCTCCCT[A/G]TGTTGCCCAGGCTAG | 55130 |
| rs547022204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27815971 | TAAACATGAATCTCT[C/T]TCCAAGTATTTTCCT | 55130 |
| rs547024380 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27849360 | TGAAAAATGAGAACA[C/G]TTGGACACAGGAAGG | 55130 |
| rs547027828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27848375 | GCTAGCCATATGTAG[A/G]AAGCTGAAACTGGAT | 55130 |
| rs547065128 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27847948 | AATGGAAGAACATCC[C/T]ATGCTCTTGGATAGG | 55130 |
| rs547080793 | snp | A/C/G | 9.97656e-05 | 0.00706207 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944212 | CGATGACAACATCAC[A/C/G]GCTACTCACCAGTTT | 55130 |
| rs547084825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27862001 | ACAGCTCTGGATAAA[C/T]AATGAAATGATTGCC | 55130 |
| rs547136299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27949604 | CAGAGCCCAGGGTGG[A/G]AGCGTGGTGCAAGAT | 55130 |
| rs547146216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27830198 | TCCTTGGTCTCCTCA[C/T]CTCCTGGTTTCCCGG | 55130 |
| rs547156949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27815310 | ATTATCATTTAAACA[C/T]GTCTTACACATTAAA | 55130 |
| rs547166429 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872817 | TTGGTCTAAAATTCT[C/T]TTTTTTTTCTGTGTC | 55130 |
| rs547185014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27835956 | AAAAGAAAATCATAA[A/G]GAAGAGAAAATACAT | 55130 |
| rs547187202 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27922078 | AGGCTGAGGTGGAAG[A/G]ATATCTTGAGCCCAG | 55130 |
| rs547189983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27820746 | GTTGGTTAAATTTTA[A/G]CTTAACAATTAAACC | 55130 |
| rs547193407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27821716 | CTCAGGAAAGTGAAC[C/T]ACAAATTTGGTACAA | 55130 |
| rs547226445 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27914911 | CCTGACCTTTTCTCT[C/T]TGAAGAAGAAGTGAC | 55130 |
| rs547228634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27853673 | AATTCAGTGAGAAAA[A/G]AGCAAACAGTTTTTT | 55130 |
| rs547238053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27814322 | ACATTCCTCCCAGTG[C/T]GCAGGCCATTTGAAG | 55130 |
| rs547274221 | snp | A/G | | | stop-gained | ARMC4 | GRCh38.p7 | 10:27860681 | CGTCTTCTGAGAGTT[A/G]GTACAAGGCCTGAGC | 55130 |
| rs547308466 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27947181 | TAAAATATGAATTTT[A/T]AAAATCCTCTCTTTA | 55130 |
| rs547325820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27820215 | GGCTCCACATGCCAC[C/T]GGCTGCTGCCACCCT | 55130 |
| rs547357278 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27834910 | GAAAGTTTTTCTGTA[G/T]TTGTGGATGGAAACC | 55130 |
| rs547357729 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27960942 | TTTTGGTGAGCCATT[C/G]CCCTTGCCCTCCTGC | 55130 |
| rs547358917 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27828676 | ATGCACCATTTATTA[A/G]AAAACAATTACCTTG | 55130 |
| rs547360749 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27920144 | TGGCACTGAGTGGGC[A/T]GTGAGGACGGGCAGC | 55130 |
| rs547399589 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27826890 | GCTAGCATCCTCACT[C/G]TCCAGCTACCACTTT | 55130 |
| rs547430718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27982620 | GAAAGATAACTATAG[A/G]TAATCAGAAAAGAGG | 55130 |
| rs547434035 | snp | C/T | | | missense | ARMC4 | GRCh38.p7 | 10:27939952 | TTCTCACTATTTAGG[C/T]TCTTGACAAGGTTTT | 55130 |
| rs547440241 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27906977 | TGTAACAAACCTGCA[C/T]GTTCTGCACATGTAT | 55130 |
| rs547442684 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27918164 | AAAAATAATTTCTCA[A/G]CTTGTCCTATAGGGC | 55130 |
| rs547477028 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27976335 | ATGATCTTTACTCAC[C/T]AACAATATCTACATA | 55130 |
| rs547501090 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27877298 | AGCACTGGGGCCATA[C/G]TGGGAAAAATGACAA | 55130 |
| rs547505307 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27915693 | AGAAGGAAAAGAACT[C/G]TCAACCTAGACTTCT | 55130 |
| rs547536345 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27890195 | CCTGATGGGGTCACA[A/G]TGCAATGGGAGTGCT | 55130 |
| rs547565070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27879858 | CCAAGCCAGCTGTCT[A/G]GTCTCCCTCATCCTT | 55130 |
| rs547570855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27934170 | CACTATAATTATGAG[A/G]CCTCCCAGCCATGTG | 55130 |
| rs547590091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27895535 | TTCCAGCTATTCACC[C/T]GCCTCGGCCTCCCAA | 55130 |
| rs547592643 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27989720 | CAGGCATGGTGGCAC[A/G]TGCTTTGGTCCCAGC | 55130 |
| rs547599255 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | ARMC4 | GRCh38.p7 | 10:27901723 | ACAAAAAAGGGCATT[G/T]CATAATGGTAAAGGG | 55130 |
| rs547634416 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27902150 | ACTCAGGATTAAGAA[A/T]CTCTCTCAAAACCAC | 55130 |
| rs547645034 | snp | A/G | | | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999761 | ACTTAGGATGATGGG[A/G]TGTTTAGGAATTAAA | 55130 |
| rs547652165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27954061 | AATGATGACAATAGA[C/T]CCATATAAAGATGTA | 55130 |
| rs547706098 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27862320 | CTCATACCTCATAAG[A/C]AATGGGTATTAAACT | 55130 |
| rs547729485 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27867818 | GCTGGGCATGGTGGC[A/G]TGAACCTGTAATCCC | 55130 |
| rs547753837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27939798 | AATAAAATGCAGATT[C/T]CTGAGTCCCATTCTC | 55130 |
| rs547766591 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27873527 | TACACACTGCTTTAA[A/G]TGTGTCCCAGAGATT | 55130 |
| rs547781143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27913196 | GGTAAATTACGTGTC[A/G]CGGGGGTTTGGTGTA | 55130 |
| rs547784836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27859534 | TAGATATGACTAACT[A/G]GGGTTTTTAACTCTT | 55130 |
| rs547801110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27812941 | TCCACCTCTCAGAAC[A/G]AGCCAACAGCATACC | 55130 |
| rs547810437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27843715 | ACAGATGCAATGAGC[C/T]GAGATCACACCATTG | 55130 |
| rs547815643 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27960428 | CTCGGCTCACTGCAA[A/C]CTCCGCCTCCTGGGT | 55130 |
| rs547817129 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27895040 | CACTAGTCATCGGTA[C/T]GAAAAAAAAAAAAAA | 55130 |
| rs547823395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27833451 | GGAAATAAAATGCAT[C/T]GTAGGAACTCAGCCC | 55130 |
| rs547840599 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27905504 | CATTCTTCACAGAAT[C/T]ACAAAAAACTACTTT | 55130 |
| rs547852572 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27842838 | ATAATTACTAAAGCT[A/G]ATTATACATATACCC | 55130 |
| rs547855437 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27930975 | AATGGCTGGAAGGCC[A/G]CTATAGACAAAACAA | 55130 |
| rs547867767 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27976727 | CCATCAGGCAATTTT[G/T]TAAGAAACTGACATG | 55130 |
| rs547877585 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27922304 | GAATTCTGCACCCCT[A/G]AGCCCTTTTTGAAGA | 55130 |
| rs547882907 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27966172 | ATTTGTGTGTAAAAC[A/T]CTATGATTATGCTCT | 55130 |
| rs547904419 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27969474 | GCTTGAAAGAGTAAG[A/T]ATATGGAAAAAGCAG | 55130 |
| rs547908170 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27936503 | AATCATGTCAGCAAG[C/G]CTCTTAGTGCCACTG | 55130 |
| rs547921617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27966715 | TCACTGAGTAATAGC[C/T]GTTGCTTGGATACAT | 55130 |
| rs547939048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27887673 | AATTTGCAGCAGAAG[A/G]AAAAGTGGAAAATTC | 55130 |
| rs547939667 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27878979 | GGAAAGGAAAATTAG[C/T]TTGGGTAAAAGAAAT | 55130 |
| rs547984228 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27848414 | TACACCTTATACAAA[A/C]ATTGATTCAAGATGG | 55130 |
| rs547989324 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27815086 | CGATCGAAGCCATTA[G/T]ACAGCAACAACTCTA | 55130 |
| rs547991405 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27813593 | TACCCAATAGCATTT[C/G]AGTGCAAATGTGGAT | 55130 |
| rs548029465 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27988408 | AGTGGCGTGATCTCG[G/T]GTCACTGCAACCTCT | 55130 |
| rs548034193 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27908129 | TACTTTCCAAAACAA[A/C]TATTTATGCCTCAAA | 55130 |
| rs548046352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27973478 | TTTTTTCTGATCTTC[C/T]CCCTCCTCCCACCCT | 55130 |
| rs548082914 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27846141 | CTCAGCACCACATCG[C/T]ACTTATTCCAAAATT | 55130 |
| rs548089738 | snp | G/T | 0.0260105 | 0.111035 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940271 | AGTATATGTGATATA[G/T]ATATAAATGCCAGTA | 55130 |
| rs548124017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27814373 | CCCGGCTGTCTCAAT[A/G]AGATTAAATAAGAAA | 55130 |
| rs548170876 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27882587 | CTTGCAACAAACAGC[A/T]TCTATTCAAGAAAAA | 55130 |
| rs548172799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27955215 | AACAAGAATAACTCT[A/G]TGCCATCACATTCTT | 55130 |
| rs548185558 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27990726 | CAGCCTTTCATGATA[A/T]CGATCACAAAGCTAA | 55130 |
| rs548190567 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27907566 | CACCAGATAAATCTG[A/T]CTTACAATAAGTCAA | 55130 |
| rs548210434 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27928766 | TTATCTTTTAAAATT[C/T]CTATTAATTGAACCT | 55130 |
| rs548230425 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997449 | TTTAAAGAAAAAATG[A/C]GAAATTAAATAGATT | 55130 |
| rs548235124 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27848858 | CACAATGAGATACCA[C/T]CTCACACCAGTTAGA | 55130 |
| rs548275912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27820875 | GCAACCTCTGACTCC[C/T]GGATTCAAGCCATTC | 55130 |
| rs548291985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27929178 | CCATACTGAAATAAC[A/G]ATCATTAGCTGCTTA | 55130 |
| rs548305954 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27891336 | CTTCTCAGTTTGGAG[C/G]AGAACTTTAGGTCAC | 55130 |
| rs548337709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27889432 | AATTCCTAAGCACAG[A/G]TATAATCATCGTAAG | 55130 |
| rs548342064 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27890670 | GATTTGAGCTATGGC[C/T]AGTGATTCTTTCGGC | 55130 |
| rs548373129 | snp | G/T | | | missense, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984274 | TCTTCACCGTCATGG[G/T]ACTTAAACTTATTTC | 55130 |
| rs548374705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27888388 | AAGATGATATCTCAC[C/T]GTGGTTTTTATTTGC | 55130 |
| rs548387053 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27990236 | CTCTGCAGCCTCGAA[C/T]TCCTGGGCTCAAGGG | 55130 |
| rs548401657 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27955127 | ATGGTACTCATTTGC[C/T]TTTCTAACTACTGGA | 55130 |
| rs548418232 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27902173 | AAAACCACACAACTA[A/C]ATGGAAACTGAACAA | 55130 |
| rs548422064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27990962 | TTCTACCAGAGAAGG[A/G]AAAAAAATCAGGTAA | 55130 |
| rs548431041 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27872210 | CACATTGATTTTGTA[C/T]CCTGAGACTTTGCTG | 55130 |
| rs548451134 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27947923 | TTTGGTAGCAATTTT[C/T]GAGCTTATACACTCA | 55130 |
| rs548469354 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27954890 | TCCAAATACTTAAAG[G/T]GGATTCACTTCTTAT | 55130 |
| rs548484912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27861718 | CTTCTTTGTATACGT[A/G]ATTGCCCTGTAATGG | 55130 |
| rs548494496 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27982389 | AATAAGTTATATGTA[C/T]GTAGATCAATAATAA | 55130 |
| rs548502964 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27928301 | ACTCATGTTCAGTCA[G/T]TCACTTGGTCCCATC | 55130 |
| rs548511587 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27821539 | TAGTTTCTTTAAAAC[A/T]AGCAAATACTCGCAC | 55130 |
| rs548516800 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27868852 | AAAATAAAATAAAAT[A/T]AAAATAAATAATAAA | 55130 |
| rs548533261 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27974716 | TTTGCTTAGGATTGC[C/T]TTGGCTATTCTTTTC | 55130 |
| rs548538704 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984088 | TAAGCTTTCCCCTTC[C/T]TAAACCTTCTCTTGT | 55130 |
| rs548544632 | in-del | -/TGTTTATTACTCTATATGTAGTA | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27855368 | AATCAGAAACAAGTC[-/TGTTTATTACTCTATATGTAGTA]TATATTCATCGATAC | 55130 |
| rs548559688 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27869377 | ATCTTTCTCCTGAAA[A/T]AAATAAAACCTGAGA | 55130 |
| rs548567651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27996731 | ATGGAATTTTACCAA[A/G]AGCTCAGCATTTTGG | 55130 |
| rs548588236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27988926 | AGCCAAACATAATCA[C/T]CAGGGTTCTTATAAG | 55130 |
| rs548603680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27853434 | TACTATTATCCACTT[C/T]AAGTGAAAAGACACA | 55130 |
| rs548606704 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27860290 | GACCCTGTCTGTATA[A/C/T]AAAATTAAAAGAATT | 55130 |
| rs548625411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27827935 | ACTTGTGCTACTTTA[A/G]AAGTTCTAGCAAGCG | 55130 |
| rs548662557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27834750 | GAGAAGGCTTGATTA[A/G]GGTAAATACAAGCTG | 55130 |
| rs548674991 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27967711 | GCCTGGCCAACATGG[C/T]AAAACCCCGTATCTA | 55130 |
| rs548688597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27906871 | CCTGTCAGGGGGTGC[A/G]GGACTAGGGGAGGAA | 55130 |
| rs548690461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27873637 | TCATTCAGGAGCAGG[C/T]TGTTCAGTTTCCATG | 55130 |
| rs548690659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27856267 | TCACACTGTATTGGA[A/G]GGGATTGATTAACAC | 55130 |
| rs548696890 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27903928 | AGAAAGACTTCCTGT[-/A]TCTCCTCTTCCTCCC | 55130 |
| rs548700380 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27842013 | TACCCTATGGCCGCT[A/G]AACAAACACTTTCCC | 55130 |
| rs548764247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27920282 | TTCCCTTATGTATAG[C/T]TTACAAATTAAAAAA | 55130 |
| rs548784681 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27922947 | AACAAACAAACAAAA[A/G]ACAAAAAAAACTAAA | 55130 |
| rs548790123 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27818983 | CTGAACCTCTTAACC[C/T]AACCTTCTCATATGT | 55130 |
| rs548809726 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27948398 | AAATATTCAACATAC[A/T]GAGCCACAAATGTTA | 55130 |
| rs548812998 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27959513 | CTGGGCATGGTCACC[A/G]TGCGTGCCAGTCTGG | 55130 |
| rs548826599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27953813 | AGTGTGCTATTTGTA[C/T]AATATTTAAAGATTT | 55130 |
| rs548834131 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27967020 | GGGTACTGGAAAAGC[C/T]GGCAAAGCAGAAACT | 55130 |
| rs548840722 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27830512 | ACAAATTTTAGAGAA[C/G]AGAGTTTTTCAGCCA | 55130 |
| rs548853860 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872359 | TATTTCTTTCTCCTG[A/C]CTGATTGCCCTGGCC | 55130 |
| rs548855378 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872705 | ATTCCAGGGATGAAG[C/G]CCACTTGATCATAGT | 55130 |
| rs548861733 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:28000666 | CCTTGGTTTGCAAAG[C/T]TGGAAAAAGCCAGAA | 55130 |
| rs548874505 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27958740 | TTACATGTGTTGTAT[G/T]TCATTTAATATTCTT | 55130 |
| rs548890237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27826445 | GCTATTTAAAACCGG[C/T]TCCACTCTCCTCAAA | 55130 |
| rs548890607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940937 | TAAAAAATCACTTTT[C/T]GTACTCCATAGCAGC | 55130 |
| rs548902948 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27846999 | TACCAGAAGTACAAG[G/T]AGGAGCGGGGACCAT | 55130 |
| rs548951068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27901111 | CAGACTAACAGTGGA[C/T]CTCTCTGCAAAAACT | 55130 |
| rs548962858 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ARMC4 | GRCh38.p7 | 10:27971836 | AATAAAACAAAAATC[C/T]TTCAAAAATGAAAGC | 55130 |
| rs548964630 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27838865 | TCTTTTATCAACAAA[A/G]AAAGCTGCGGGACAT | 55130 |
| rs548991452 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27846008 | TGTCAACATTAGACA[A/G]ACCAATGAGACAGAA | 55130 |
| rs548996134 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27878752 | TTAAATCCTTTAAAA[A/T]TTCTCAATACAGCCT | 55130 |
| rs549004195 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27852827 | GTAGTCAGGCATGGT[A/G]GCATGAGCCTGTAAT | 55130 |
| rs549042831 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27859677 | AGGCTATAGAAAAGA[A/G]CTAATATTTTAAATC | 55130 |
| rs549047073 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27953125 | TAAATATATCCATCA[C/T]CTGAAAACATGTCCT | 55130 |
| rs549049341 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27926009 | AGACTCCAGCTAAAA[A/T]AAAAAAAAAAAAAAA | 55130 |
| rs549056661 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | ARMC4 | GRCh38.p7 | 10:27938738 | CTGAGCAACTGGGAT[G/T]ACAGGCACATGCAAC | 55130 |
| rs549058578 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27945401 | AAGGAAAACGTGCAG[A/G]AAGCAGCACCGCAAT | 55130 |
| rs549075640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27924927 | CATAGGAGACTTCTA[C/T]CAAACCTTCAAAGCC | 55130 |
| rs549077946 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27946396 | TTTTAATTTTTAAAA[A/G]TTTATATATAATAGT | 55130 |
| rs549088516 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27859561 | TCTTTGCTAAACCAA[C/T]AAGTCCACTTTGGGC | 55130 |
| rs549090712 | snp | A/C | | | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:28000203 | GTGATCCACCCACCT[A/C]GGCCTCCCAAAGTGC | 55130 |
| rs549095701 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27939514 | TGAAGCCAGGGGTTT[C/G]AGACCAGCCTGGGCA | 55130 |
| rs549108450 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27886027 | GTGAACATGAACACA[A/G]GTCATTTGAAATTAT | 55130 |
| rs549146248 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27819349 | GAAAGATTATTTTAA[A/C]GGCAACTCTGGGGTG | 55130 |
| rs549163221 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27877268 | GTTGCTTCATCAGTA[A/G]AGACAATCAGCCACA | 55130 |
| rs549167421 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27978970 | ATCCCAGCACTTTGG[C/G]AGGCCGAGGCAAGCA | 55130 |
| rs549171735 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27851370 | AGATATCCTGTTCCC[C/T]CAAAAAATAAAAACC | 55130 |
| rs549172519 | in-del | -/TATACT | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27958094 | GAAATCATTTATAGA[-/TATACT]TTTCCTTTTATTGGC | 55130 |
| rs549176714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27919278 | CTTTCATGCCATACT[C/T]AAAAACTAGTTTGAT | 55130 |
| rs549184858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27818802 | CTGGAAAGAAGTGAA[A/G]TAAAGTCCTAGTCCA | 55130 |
| rs549281759 | snp | A/T | 1.7433e-05 | 0.00295232 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944474 | CGAATATGTAACCCG[A/T]GCTATGTTTTTAAAA | 55130 |
| rs549306189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27817638 | TAAGGGCCTCCAGTT[C/T]CATTTATGTTGCTGC | 55130 |
| rs549306235 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27824712 | AAATTGCCCTCTTGA[A/T]ATAAACTCTGAATAT | 55130 |
| rs549311584 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27882073 | ACTCAGGAGGCTGAG[A/G]TGGGAGGATCACTTG | 55130 |
| rs549315526 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27912554 | AATGTGAACAGTTTG[C/T]GCCCATACTGTGGGC | 55130 |
| rs549325301 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27932595 | GGTGGTTTCTCAGGC[A/G]AAGCCCAGTTCCATC | 55130 |
| rs549338023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27918512 | TATTTTTATTAAAAT[A/G]TAACTCTCACAGCAA | 55130 |
| rs549353944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27979603 | AAAATAAAATTTAGA[A/G]AACAATTTCATTTAC | 55130 |
| rs549378896 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27982475 | TCCTTCTTTTGTCCC[G/T]TTATTCCTAATTAGA | 55130 |
| rs549388297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27857547 | TTAAAGTGTGACTGC[C/T]AGAAAATTTAATATT | 55130 |
| rs549393469 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27976971 | TTTGACAAAGTTATA[A/G]AGGTAATTCAGTGAA | 55130 |
| rs549396289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27951144 | GAATGGTCATACCAT[A/G]TGCCTGAACTATTGG | 55130 |
| rs549397524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27854153 | TAATCATTAGAAAAA[C/T]TGAAATTGAAATCAT | 55130 |
| rs549448878 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27849447 | AGGAGATACACCTAA[G/T]GTAAATGACGAGTTA | 55130 |
| rs549455667 | snp | A/G | 3.34594e-05 | 0.00409006 | missense | ARMC4 | GRCh38.p7 | 10:27987517 | TGTCCATTTTTATCA[A/G]CTTCTTCTGATTTGA | 55130 |
| rs549460216 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27850656 | TCTAAGAGAAAATAT[A/C]AAAAGAAAAGACTGC | 55130 |
| rs549461297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27904329 | CGGGGAACATGGCGT[C/T]ATGGCAGGAAGCAGA | 55130 |
| rs549465186 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27951159 | GTGCCTGAACTATTG[A/G]AATTCAACATTATTA | 55130 |
| rs549471856 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27941643 | AGTCACTGAAGATCT[G/T]AAGGGAAAGGCAATT | 55130 |
| rs549489769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27989612 | ACTCCTGGTGAGAAG[C/T]CAAAGGGCACAGGTG | 55130 |
| rs549506375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27847907 | CTACAAACCACTGCT[C/T]AACAAAATAAAAGAG | 55130 |
| rs549508936 | in-del | -/A | 0.000608327 | 0.0174297 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944440 | ACCAATCTGTGTGAG[-/A]AAAAAAAAAGATGAG | 55130 |
| rs549537483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27894019 | GCATGGTGGCTCAGG[C/T]CTGGAGTCCTAACTA | 55130 |
| rs549542021 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27904832 | ATTTATAAATCAACT[C/T]GGAGGGAATGGGCAT | 55130 |
| rs549587416 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27827590 | TCCAAAATGTCACAA[A/T]CTCCTCTTGTTTTTA | 55130 |
| rs549591320 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ARMC4 | GRCh38.p7 | 10:27858121 | CTAGGCTGAAATCTG[G/T]AATCATTTTTTTTAC | 55130 |
| rs549592802 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ARMC4 | GRCh38.p7 | 10:27813395 | ATTTTTCCCTTTTCA[A/G]CAGATAATTGGCTTA | 55130 |
| rs549610023 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27859828 | TCCTGTCTACTGATG[A/C]ACAGATTTAAACAAA | 55130 |
| rs549619492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27987006 | TCCTTGGCAGTATGC[C/T]GAGAGAGAGTGGATT | 55130 |
| rs549649498 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27996564 | CAGGCATCTAGTAAG[C/T]GAAAAACTTCAGATA | 55130 |
| rs549665229 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27960316 | ATTTATTTATTTCAT[C/T]ATTATTATTATTATT | 55130 |
| rs549671082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27951772 | TTATTAATGTACAAA[A/G]GAGTAGACAAAAAGA | 55130 |
| rs549688407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27913125 | CATATAGTAAATATG[C/T]TTCTCCTTTTTTCAA | 55130 |
| rs549695384 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999741 | TTAAGGACCAATGCC[A/G]GAGCACTTAGGATGA | 55130 |
| rs549715538 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27871317 | GGTTGCCTGTTCACT[C/T]TGATGGTAGTTTCTT | 55130 |
| rs549730566 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27926338 | GATATAGAATTATCA[C/T]ACAGAATTCAACGGA | 55130 |
| rs549735158 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27834463 | ACCTAATCATCACAC[A/G]GCCACACCAAGACTC | 55130 |
| rs549741646 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27993013 | CTCCACCTCCCAGAT[G/T]CAAGCAATTCTCCTG | 55130 |
| rs549742436 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27841462 | GTGCAGTGGTGCGAT[C/G]TCAGCTCACTGCAAC | 55130 |
| rs549754357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27867713 | TCAGCACTTTGGAAG[A/G]CTGAGGCAGGCGGAT | 55130 |
| rs549759211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27912391 | GATGAATACATGTAC[A/G]TGCTTTTGGTTATTT | 55130 |
| rs549759506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27833392 | GAAAAAAAAAATCAA[A/G]GAGGAAAATTAAACT | 55130 |
| rs549780423 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27832745 | AAGGACTTAATGTTG[C/T]ATTTCAGCAGGATAC | 55130 |
| rs549793254 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | ARMC4 | GRCh38.p7 | 10:27873398 | CTTGCCTTCTGCTAG[C/T]TTTTGAATGTGTTTG | 55130 |
| rs549814834 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27895327 | CCTATTTGAGATGGA[C/G]TCTAGCTCTGTCACC | 55130 |
| rs549819082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27838906 | GAACAGATCCAAGGA[C/T]CTACAGGTCGTCAGG | 55130 |
| rs549848434 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27920046 | AGGGATGAATTCTCA[A/C]GTATAAAATTATGAA | 55130 |
| rs549857457 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27901679 | AGTCTCTGATAAAAC[A/G]GACTTTAAACCAACA | 55130 |
| rs549871181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27941041 | CAAGAAATGTAAGCC[C/T]ACCAAGATAGTATTT | 55130 |
| rs549885574 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27989058 | TAGGGGCCTCTAGAA[C/G]CTGGAAAAGCAAAGA | 55130 |
| rs549885644 | in-del | -/TAAAA | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27843231 | TGGAGTACAAAGTCT[-/TAAAA]TAAAAACAGCCTATC | 55130 |
| rs549894831 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27946375 | ATTCAACACAATAGG[C/T]CAAGTTTTTAATTTT | 55130 |
| rs549936964 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27903648 | TAAGCATTCCTATAC[A/C]CCAATAATAGACAAA | 55130 |
| rs549939990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27840106 | TAAAACCAGCCAAAG[C/T]TGTCAGCAAGAATTT | 55130 |
| rs549950568 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27916240 | AGGGCAGACATACTA[A/G]GGGAAGGTGGCCTAA | 55130 |
| rs549995505 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940082 | ATTTATTAATAAACA[C/T]GCTGAACAAACTTTC | 55130 |
| rs550007316 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27826735 | CTGCGCCATTAACCC[C/T]CCTCTTTCCGGTATT | 55130 |
| rs550074490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872783 | TTGAGGATTTTTTCA[C/T]CGACATTCATCGGGG | 55130 |
| rs550076650 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27838120 | ATATTTTTGGCACAT[C/T]AAAAACTCCAACGTA | 55130 |
| rs550090988 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27912468 | CTCAGGCTCTTGTTA[G/T]GTTAACATTTTCCAG | 55130 |
| rs550112692 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27902709 | CGAGAAGAAATGGAT[-/A]AATTCCTGGACACAT | 55130 |
| rs550160928 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27878857 | AACAAATCCAACAAC[G/T]TTAAAAAAAATTATT | 55130 |
| rs550161641 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27899923 | CTGTCTGCTGGCTCT[A/G]AAGAGAGCAGTGGAT | 55130 |
| rs550178122 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27904951 | GGTTTTTCTTAAGTC[A/C]TTTAACATAAATATT | 55130 |
| rs550194049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27945001 | AAGGTTAAGGAACAC[C/T]GCATTCCCATAGAAA | 55130 |
| rs550249413 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27957856 | TCTTTTTTTTTCCAA[C/T]AATCAGAGACATCAC | 55130 |
| rs550271863 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999890 | TCTGCAAACACGTAG[C/G]GATATGAGGTATAGA | 55130 |
| rs550295599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27887580 | ACCATATATGAAGCC[A/G]CAAAACAAGTCTTTA | 55130 |
| rs550310643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27939686 | GAAGTGACAGTGAGC[C/T]ATGATTGTGCCATTG | 55130 |
| rs550331968 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27887016 | CAGCAAAAATAAGTG[A/C]TTTCCTATACTTTAA | 55130 |
| rs550341189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27900510 | GAGTAATAACAAACT[C/T]GTCTGAGCTAAAGGA | 55130 |
| rs550343532 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ARMC4 | GRCh38.p7 | 10:27846014 | CATTAGACAGACCAA[C/T]GAGACAGAAAGTTAA | 55130 |
| rs550344664 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27951839 | CAGCACTTTGGGAGG[C/T]CAAGGCAGGTGGATC | 55130 |
| rs550382312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27851548 | TATTGCAGATGTAAA[A/G]CACACTAGATGGCAA | 55130 |
| rs550465327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27876906 | GCATCTGTAGCCTTT[C/T]GTTCTTCATATTGTA | 55130 |
| rs550466205 | snp | A/G/T | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27858929 | CTGCCTCAGCCTCCC[A/G/T]AGTAGCTGGGACTAC | 55130 |
| rs550470306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27952456 | AGGTTTGTTACATAG[A/G]TAAACGTGTGCCATG | 55130 |
| rs550474805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27945561 | AAATCCTGGCTGAAC[A/G]CAGAGTCTTGCAAAC | 55130 |
| rs550489243 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27994857 | GCCCCCAAACCTAGA[A/C]CCAATTGATAATACT | 55130 |
| rs550491826 | snp | A/G/T | 6.65783e-05 | 0.00576935 | intron-variant | ARMC4 | GRCh38.p7 | 10:27971064 | AATTAGGTGAGTATG[A/G/T]TTACTAATGCTGCAT | 55130 |
| rs550498937 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27970624 | AAGGAATCAACCTGC[A/G]CCTTGGAGGGACATG | 55130 |
| rs550501803 | in-del | -/AAAAAAAAAAAAAAAAA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27943813 | AAAAAAAAAAAAAAA[-/AAAAAAAAAAAAAAAAA]GGCATCATAGATGTC | 55130 |
| rs550532697 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27892594 | TTACATACTTGCTTT[C/T]TCCAAAATGAAGTTT | 55130 |
| rs550542420 | snp | C/G/T | 0.00128756 | 0.0253406 | synonymous-codon, missense, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27985060 | GAGGAGGTGCAGATC[C/G/T]AATTGCTTAAGCAGC | 55130 |
| rs550557357 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27978156 | TGGCATATCCATACA[A/G]TGGAATAATACACAT | 55130 |
| rs550572834 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:28000398 | GGTATACAGAGAAGC[A/C]CTTTTAAAAATGGGT | 55130 |
| rs550579503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27985843 | AAATACCAATTCATT[A/G]TCAAGGCTGATACAG | 55130 |
| rs550593066 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27903644 | GTCATAAGCATTCCT[A/T]TACACCAATAATAGA | 55130 |
| rs550609481 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ARMC4 | GRCh38.p7 | 10:27992957 | GAGTTTCTCTGTCAC[C/T]CAGGCTGGAGTTCTG | 55130 |
| rs550634225 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27958442 | CCGTGCCTGCCCCAT[A/T]AAATCCTAAGGGAGA | 55130 |
| rs550635740 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27871562 | GGGATCCAGTTTCAC[C/G]TTTCTACATATGGCT | 55130 |
| rs550640521 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27865083 | CCCCTGCCCTTAGGA[A/T]AAAATTCAAACTCCA | 55130 |
| rs550654731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27832013 | ACAGTCAAGCATATT[C/T]GGGGCTTCCCCTGAA | 55130 |
| rs550678371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27863459 | ATTTTTCACTTCTCT[A/G]TGCATGTCCAAGAAT | 55130 |
| rs550689773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27899001 | CCTTTATATAAAAAT[A/G]TTCAACAAGACCTAG | 55130 |
| rs550694260 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27917482 | AAAAAGAAGCAAAAG[G/T]TAAACACAAATAAGT | 55130 |
| rs550704178 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27992025 | TCATAGCAAACACTG[A/C]GTGGCTATGGGTTAC | 55130 |
| rs550750423 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27903783 | AGATACAGCTGAGGC[C/T]CCACCAATACATGCA | 55130 |
| rs550751839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27924740 | AGATTAGTTTGCAGG[C/T]CACTATTCAAATAAA | 55130 |
| rs550758196 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27931938 | AATATAAATCAAAAG[A/T]GCATTTAATATACCT | 55130 |
| rs550785173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27950026 | AGATTGATCAGGACC[A/G]GAGGCCTCTTGTTCT | 55130 |
| rs550791076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27838021 | AAGAATCTAAGATTT[C/T]TGTATTTTTTTAAAT | 55130 |
| rs550808445 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27862773 | TATTATATATTATTT[C/G]TACATGTATATGTAT | 55130 |
| rs550819320 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27963877 | GTCTCATTTTAATTC[A/T]CTCAACAATCTATGA | 55130 |
| rs550826768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27962725 | CTACGTCCCTGCAGA[A/G]GTCCCTCATGCACAC | 55130 |
| rs550854321 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27931270 | AGCATTTTGCAGGTG[C/T]GTTTTACATTTTAAA | 55130 |
| rs550863569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27956161 | CAGGGGCAAGGATGA[A/G]TGTGTAGGAATGGCC | 55130 |
| rs550873565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27963229 | GGCCAGGCTGGTCTC[A/G]AACTCTTGACCTCGT | 55130 |
| rs550882466 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27937716 | TGTCACCCATGGAGG[A/C]CACTAGAAGAAATCC | 55130 |
| rs550913926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27822674 | ACAGCTCACCAAAGC[C/T]GGGGGCCTCAAAACA | 55130 |
| rs550944092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27904252 | CTTTCTGTAAGAAGT[A/G]TGGCAAGCACCAACC | 55130 |
| rs550945486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27905798 | ATAAGTGGTGTTGGG[A/G]AAACTGGCTAGCTAT | 55130 |
| rs550945660 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27937173 | GGTCAGTGGAAAACC[A/T]ACAACTCCACTAGCA | 55130 |
| rs550977342 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27869707 | GTCCGGCTAATTTTT[G/T]TATTTTTAGTAGTGA | 55130 |
| rs550980873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27899341 | GAGATTCCCTCAGGC[A/G]CCCACACCACCAAAG | 55130 |
| rs550982366 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27900540 | AGCATGTTCTAACCC[A/C]AGGCAAGGAAGCAAA | 55130 |
| rs550982867 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27845183 | AGAGAAACAGTGGGT[C/T]ACACACAAAGGGAAG | 55130 |
| rs550984357 | snp | A/G | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27995258 | TTCTCAAGACTTTAA[A/G]CTAGTACTCCCCATC | 55130 |
| rs551021138 | in-del | -/AACATTGTTACTTAGTTTAAAAGATGCTTTGG | 0.0166325 | 0.0896639 | intron-variant | ARMC4 | GRCh38.p7 | 10:27859243 | TATAGTTTACTTTTA[lengthTooLong]CCAGATTTTTGCTTG | 55130 |
| rs551095650 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999055 | GCACCGTATGCCCGC[G/T]CCAGAGACGCTCTGC | 55130 |
| rs551107619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27870261 | CTTTTCTCTCCCAGT[C/T]TTCTCTTTGGCATAG | 55130 |
| rs551112398 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27906239 | AGAAGACATTTATGC[A/G]ACCAACAAACGTATG | 55130 |
| rs551120921 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27871737 | TTTTGGTACCAGTAC[C/T]ATGCAGTTTTGGTTA | 55130 |
| rs551127814 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27948715 | AAAATTAATGCAATT[C/G]TTTTGCTAGTTGTCT | 55130 |
| rs551175412 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27908978 | TTTTCAAACCTAAAA[C/G]TTTCATACCATGCTG | 55130 |
| rs551177951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27830942 | CATCTTTTGGATAAG[C/T]TTGGCAGGTGGACAG | 55130 |
| rs551194497 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27924233 | AAAAGTAAAATTCTC[C/T]GTGTAGTTAAAAAAA | 55130 |
| rs551210476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27865193 | TCCAACCTCCCCCAC[A/G]TATACCCTGAGCCAG | 55130 |
| rs551227607 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27970101 | GAGATTCTGTCTCAA[A/C]AAATAAATAAATAAA | 55130 |
| rs551239437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27860503 | AATGCAGCCATGATG[C/T]AGCAGGCAGGCACTT | 55130 |
| rs551250957 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27872385 | TGGCCAGAACTTCCA[A/T]CACTATGTTGAATAG | 55130 |
| rs551358774 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27978270 | AAAAATTATAGAACA[A/C]CAAGGAAGATCCTAA | 55130 |
| rs551362360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27818726 | CATGGCCACCCGCCT[C/T]GCTTCTGCTCCAGTC | 55130 |
| rs551397337 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27978886 | CTAACATCAGGCTCA[A/G]TGGTGAAAGCCTAAA | 55130 |
| rs551397446 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27850546 | TGGGTGACAGAGCGA[A/G]ACTCTGTCCCAATAA | 55130 |
| rs551434243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27850188 | GGCGGCTCACACCTG[C/T]AATCTCAACACTTTG | 55130 |
| rs551441876 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27866558 | TAATTTATAAAGAAG[A/T]TAAGTTTATTTGGCT | 55130 |
| rs551453963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27884776 | AGCTGGGGTGAGCCT[C/T]TTTGGAAAATTAAGG | 55130 |
| rs551463200 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27939731 | CAACAGAGCAAGACC[C/T]TATCTCTAAAAAAAT | 55130 |
| rs551471731 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27857512 | CTAAAATTAATTTCA[C/G]TGTTTCCTTTTATCT | 55130 |
| rs551476027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27837569 | AGGTATAAATACAGA[C/T]TAAGGCATCAAACTG | 55130 |
| rs551481802 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944760 | ACCTAGAGCTAAGAA[C/G]AGAGCCCAGGAAGGT | 55130 |
| rs551485004 | in-del | -/A | 0.143622 | 0.226238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27921521 | TGAATTCCAGTAATT[-/A]AAAAAAAAAAATCCT | 55130 |
| rs551490600 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27893257 | AAGCAATATTCACAT[A/C]TTATTTTCTTAACAC | 55130 |
| rs551519242 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27844982 | TAGGCACATTCAATT[G/T]TTCCCAAGTGCTCCT | 55130 |
| rs551532972 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27966277 | AGTAGATCAGGTCTA[C/T]TCAAGAAGTGACTTA | 55130 |
| rs551539403 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27841333 | CACCATTTCTCATGC[A/G]CTTACAGCTCACCAG | 55130 |
| rs551545061 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27986089 | GAAGGCATTAACATT[A/C]CCATGTGGTCATGGG | 55130 |
| rs551582835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27824973 | CCTACTTGACATCTC[C/T]ACTTGGATATAAAAA | 55130 |
| rs551604238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27937779 | GTTTATCTTCTGCAC[A/G]TGATTTTCAATTCTG | 55130 |
| rs551604586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27838132 | CATTAAAAACTCCAA[C/T]GTACTAATTCAAGCA | 55130 |
| rs551655334 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27859922 | TCCATCTAGTTATTG[C/T]TTCAGCCAGTTCCTT | 55130 |
| rs551661405 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27950056 | TGTCCCTACCCCACA[C/T]AGCTTCTCCATCTGC | 55130 |
| rs551711971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27992780 | GGAAATAGTGATAGA[C/T]TTGAGAGGTGTGTGT | 55130 |
| rs551716619 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27856947 | ACTCCAGCCTGGACG[A/G]CAAGACCGAAACTCC | 55130 |
| rs551729276 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27923322 | GATATATCAAGCAAA[C/T]GGAAACAGTAAGAAA | 55130 |
| rs551743359 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27954760 | AGATTCCCCTTTGGG[A/G]AAGACGGAGAGGAGC | 55130 |
| rs551750025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27845426 | CCTGAAGGAAGCACT[A/G]AACATGGAAAGGAAC | 55130 |
| rs551801393 | snp | A/C | | | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999362 | GCTTCCAGACAAGTG[A/C]GTTGTATGTACCTGA | 55130 |
| rs551804668 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27951682 | ATTATTTTTGTCCAT[C/T]TAGAATGGCTTCAGA | 55130 |
| rs551813627 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | ARMC4 | GRCh38.p7 | 10:27993662 | CTCCAGAAAAAAAAA[A/T]AAATAAATAAATATG | 55130 |
| rs551830719 | in-del | -/ATAT | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27961012 | ATGTAAAATATTCTC[-/ATAT]ATGCTATCTGACGTG | 55130 |
| rs551834297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27909432 | GTAAAATTAGATCTA[C/T]CATTTACCATTTTCA | 55130 |
| rs551854051 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27930038 | GCTCTCCTTGGGTTC[A/C]ATATTTATACATTTT | 55130 |
| rs551877053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27970168 | TAGGTATTTCTGACT[A/G]CCCCAGCATTTACGT | 55130 |
| rs551890116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27930855 | TTGAGCATTCAAACA[A/G]TCAATCTGGTTTACT | 55130 |
| rs551893249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27915674 | ATGGCATTTATAAAA[C/T]GCTAGAAGGAAAAGA | 55130 |
| rs551915479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27963277 | CTCCCAAAGTGCTGG[C/T]ATTACAAGCATGAGC | 55130 |
| rs551942929 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27875330 | TTGGAGAAGTTTGAT[A/C]TTCTGAAGCCTTCTT | 55130 |
| rs551945554 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27841598 | ACGGGGTTTCACCAT[G/T]TTGGCCAGGCTGGTC | 55130 |
| rs552023349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27904322 | GTATGCGCGGGGAAC[A/G]TGGCGTCATGGCAGG | 55130 |
| rs552032877 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27870860 | TTCATAATCCTTTGG[A/G]TATATACCCAGTAAT | 55130 |
| rs552083245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27843735 | TCACACCATTGCACT[C/T]CTGCCTGGGTGACAG | 55130 |
| rs552160678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27876016 | GGCACCCGCCATTGC[C/T]GAGGCTTGAGTAGGT | 55130 |
| rs552204831 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27969677 | GTTTGCTTCCAAAAC[A/C]CAATGACCCTGTGAT | 55130 |
| rs552206012 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27913819 | AATGGCTATTATGAA[A/G]AAGTCAAAAAATAAC | 55130 |
| rs552210142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27943102 | AACAATACAGTAAGA[C/T]AACAGCTCTGGGTGA | 55130 |
| rs552211692 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27955830 | TGAAAAATGTCCTTG[C/T]CAAGAATCCACCTCC | 55130 |
| rs552222981 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27838762 | TACTTTATTTTACCA[C/T]ACTGTTTGTGTATTT | 55130 |
| rs552246043 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27937078 | TCCTTATGTGGCTTT[G/T]GGAATGGATAGCAGT | 55130 |
| rs552273762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27875078 | CTTTTTTCTCTAAAC[C/T]TCTCTTCTCGCTTCA | 55130 |
| rs552280748 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27892423 | CCTGTCTTAAATTAT[G/T]TCGAGGTTTACAAAG | 55130 |
| rs552286304 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27865804 | TAAATGGTGAAGGCA[C/G]GACACGAGTCAGGTT | 55130 |
| rs552289726 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997887 | AGCACACACCTTTGA[A/C]GTAAAGAAAGTAAGT | 55130 |
| rs552293638 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27821677 | CTAATCTCTTTGTCA[G/T]AATTACATAAAAGGA | 55130 |
| rs552298789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27875700 | TTGGACAGTGGCTGC[A/G]GGACAGTGGGTGCAG | 55130 |
| rs552310762 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27874333 | GTCTGTGTCTTTTAA[C/T]TGGAGCATTTAGTCT | 55130 |
| rs552310860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27881632 | ACAGAGCAAAATCCC[A/G]TCTCAAAAAAACACT | 55130 |
| rs552333669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27882715 | CAACCTTGCAACCGC[A/G]GAATCTGGGGAAATC | 55130 |
| rs552338814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27861967 | TCATTGTCTCTCAAG[A/G]CTGCTTATTCTGTCT | 55130 |
| rs552403618 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27949448 | AGGGAAAGAACATCT[C/G]AACTGAGATCTGGAC | 55130 |
| rs552404837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27974821 | ATTGAATCTATAAAT[C/T]GCTTTGGGCAGTATG | 55130 |
| rs552406414 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27898743 | ACATATTTGTGATAT[A/G]TATTGATATTGACGA | 55130 |
| rs552415736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984622 | ATTTGTGTAATAGTC[C/T]TGAGAGCATTTGAAA | 55130 |
| rs552431961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27942384 | TTTAGAAGTCTGGTG[A/G]TATTTTTGTGACCAG | 55130 |
| rs552434465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27848905 | AGTCAGGAAACAACA[C/T]GTGCTGGAGAGGATG | 55130 |
| rs552469826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27855519 | CAGCGACATTAAGAG[C/T]TTTAATTAACAGGAA | 55130 |
| rs552471654 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27848494 | CATTCAGGACATAGG[C/T]ATGGGCAAGGACTTC | 55130 |
| rs552506781 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27921610 | AATGGATTTTTTTTT[A/T]AAAAAAGGAGGAATA | 55130 |
| rs552510581 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27854926 | AAAAACCAAGTACTT[A/C]CTGTAGGAACCCATT | 55130 |
| rs552527338 | snp | C/T | 0.00097292 | 0.0220344 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27968942 | GTAATTGTGCTCTTC[C/T]GTGTGAAACAGATGG | 55130 |
| rs552530516 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997508 | TATAGTAACTTCTTG[A/G]AGGACCCTTAACACA | 55130 |
| rs552536191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27817237 | TGTATAGCTATTCAC[A/G]CTTAAATCCCTTTCC | 55130 |
| rs552546395 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27818649 | TGCCCTATATTTGTT[A/G]TTTAGGTAATAGGAG | 55130 |
| rs552557682 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27889289 | ACTCGGGGTAGTTGC[-/T]TAAAGCAGGGGCTTG | 55130 |
| rs552572748 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27816254 | AGTAATTGCCTAAAT[A/T]GTGAAATTCACTAAT | 55130 |
| rs552572787 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27823508 | AACCTTAGTTTTCTT[A/C]TCAGTAAAATTAGGA | 55130 |
| rs552629028 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27889558 | TATGATCTCATGGGT[C/T]TCTACTGGTGGTGTT | 55130 |
| rs552664643 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27868466 | TGGATAAAGAAAATA[C/T]GGTAGATATATACAC | 55130 |
| rs552669931 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27994192 | AATTTTTTTTCATCT[C/G]AGATTTGAAAGGCTC | 55130 |
| rs552680994 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27820971 | TTTTAGTAGAGACAG[A/G]GTTTTACCATGTTGG | 55130 |
| rs552730267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27967760 | GCTGAGTGTGGTAGC[A/G]CACGCCTGTAATTGC | 55130 |
| rs552746214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27829406 | TTAACCTCATTCTCA[A/G]GGCCTCCTTGGCCTT | 55130 |
| rs552750778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27915217 | AAGCAACCAAAGAAA[A/G]AAAATGCATACGTCT | 55130 |
| rs552767666 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27961191 | GGCTCAAAACTGTAA[C/T]GTTTCAACAGCTACG | 55130 |
| rs552776896 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27929037 | CCATTATACACTATA[C/T]GTATGAACAAAATGG | 55130 |
| rs552783012 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27828907 | CACAGTATTCCTTAA[C/T]ATTAGAAAAAGTATA | 55130 |
| rs552784857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27835424 | ATAACAACAACAACC[A/G]CTGCAGCAACATTCA | 55130 |
| rs552786343 | snp | C/T | 1.76742e-05 | 0.00297268 | intron-variant | ARMC4 | GRCh38.p7 | 10:27994903 | ATCAAATCCTAGAAG[C/T]AAGTAACTGGCTTAC | 55130 |
| rs552789127 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27946013 | ATTATCTATTGTGTA[C/T]ATATATATAATTATG | 55130 |
| rs552809762 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27848760 | ATGAACAGACACTTC[C/T]CAAAAGAAGACATTT | 55130 |
| rs552823543 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27834866 | CATAGAGTCTCCAAA[G/T]AAATTGCCTGGAAGC | 55130 |
| rs552833354 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27909101 | AAAAGTCATACTGCC[A/T]TCCATATGCTACTTA | 55130 |
| rs552864413 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27922183 | AGAAAGAAAACAAAA[C/G]AAAAAAGAAAAAAAG | 55130 |
| rs552879836 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27921834 | CAATAGAGCAGTATT[A/T]TATTTTTTTTTTTGT | 55130 |
| rs552887846 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27991718 | CAAGGAGAGGCATCC[G/T]CCTTTACTTTAAAGT | 55130 |
| rs552910135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27909559 | CCAGTGACTCACACC[C/T]GTAATCCCAACACTT | 55130 |
| rs552925041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27891030 | CAGAGCTTGTGTTTA[C/T]AGCAATATTCCTAGC | 55130 |
| rs552935235 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27897725 | GAGAGGGCAGTTCCT[C/G]GTGAGAGATGTGATC | 55130 |
| rs552938392 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27928358 | TTAACCTATCGATTT[C/T]TCTATTTTTATTACA | 55130 |
| rs552960568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27863562 | TGTGGATCGACTTTA[C/T]ATATTCTTTTGCCAT | 55130 |
| rs552973083 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27998687 | CCCCGGGAGGGAAAG[C/G]GGAGCAGGCGAGAGC | 55130 |
| rs552973391 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27970940 | TGGCACCACTGCACT[A/C]CTGCCTGGGCAACAG | 55130 |
| rs552979821 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27950368 | CATTGCTTTCCTTCT[C/G]TTTATTTGCAAATCT | 55130 |
| rs552984986 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27929529 | AGGTTTCCACTGGTA[G/T]CTTTTAGCCATAGTT | 55130 |
| rs553009807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27992178 | CTTGGTTTTCATCAG[C/T]GCCAGGCAAGCATGG | 55130 |
| rs553017989 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27898790 | CATTGATTTTTCACT[A/G]CTGCAATGTATAACA | 55130 |
| rs553043152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27957075 | ACCATCTCCTTTAAT[C/T]TCTGGAAGTGATCAA | 55130 |
| rs553095781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27863132 | TTTCATATATATTGT[C/T]CATTCATTCATATTG | 55130 |
| rs553100656 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27897154 | TCCTGGTTTTCCCAT[A/C]CCCTTCCCACCCGCC | 55130 |
| rs553113361 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27976303 | AACAGTTAAATTAGG[A/C]AGGAAGAAATAAGAA | 55130 |
| rs553118858 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27874515 | TCCTTTCCATGTTTA[A/G]TGCTTCCTTCAGGAG | 55130 |
| rs553123873 | snp | C/T | | | missense | ARMC4 | GRCh38.p7 | 10:27985137 | TAATTTTGCCAAGAA[C/T]ATTTAATGCAATTGA | 55130 |
| rs553130300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27869862 | TCTAAGGGAAAGAAT[A/G]AGACATTATCATTAG | 55130 |
| rs553153993 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27883614 | CTTGAAAATCAGTTA[G/T]TATAAACATATTTGC | 55130 |
| rs553158064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27989888 | GAAAAATAAAAAACG[C/T]CAGCTATGGACAAGA | 55130 |
| rs553162062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27902326 | TTAGAGGGAAATTTA[C/T]AGCACTAAATGCCCA | 55130 |
| rs553167391 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27869467 | TATTCTGGTACAACT[A/T]CTGGACTTAAAAAAA | 55130 |
| rs553181819 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27901689 | AAAACAGACTTTAAA[A/C]CAACAAAGATCAAAA | 55130 |
| rs553189900 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27903762 | TCCAGTGCGGTACCT[C/T]CTATTAGATACAGCT | 55130 |
| rs553203837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27969800 | GCTGCAACTTGTAAA[C/T]TATTTGTTAAGCTTT | 55130 |
| rs553239676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27868567 | GCCATCATCCTCAGC[A/G]AACTAACACACGAAC | 55130 |
| rs553240797 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27962909 | GTTTCCCACATATTC[C/G]TCATCTCACAGGACA | 55130 |
| rs553249065 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27931498 | GTCTGTCTACCCAGC[C/T]CAATCAGGTCCTTCA | 55130 |
| rs553259903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27930450 | GCCCAAGCATTCAAG[A/G]CTGCAGTGAACAATG | 55130 |
| rs553264617 | snp | A/G | 6.60349e-05 | 0.0057457 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27907714 | TGCGCTGGCCTTCAC[A/G]TCTGGGTGAGGATTT | 55130 |
| rs553270650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27814535 | TCAGAGTTACATCTG[A/G]GCCCTGATTTTTCAT | 55130 |
| rs553280369 | snp | C/G/T | 0.00199529 | 0.0315338 | intron-variant | ARMC4 | GRCh38.p7 | 10:27849864 | GTCGCAAAAGCTACT[C/G/T]TAAAATAGGAGCTTG | 55130 |
| rs553282720 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27868131 | AAAATCACAATGAGG[C/T]ATCATCTCATGCCAG | 55130 |
| rs553314433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27843370 | TGAATGCAATTGTAG[C/T]GGATGGTGTAGTGTA | 55130 |
| rs553352046 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27967357 | GAACTGTGATATCAG[C/T]AGAGCCCACTGACAA | 55130 |
| rs553368492 | in-del | -/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27819020 | GGATCACATACCTCT[-/G]GGGGTCACTGCAAAG | 55130 |
| rs553375057 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27955623 | GTAATTGACTGCAAA[A/G]TACATCAAATTCCTA | 55130 |
| rs553382990 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27968102 | TAACAATATTTCAAC[A/C]AGCTATATGAACATG | 55130 |
| rs553383827 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27816215 | TCTTGTCCCTGTCTG[A/T]TGAACTATTCATACT | 55130 |
| rs553398289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27955031 | GTTGTCCTATTCGTT[C/T]GTCACTGACTTTTTA | 55130 |
| rs553406958 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27855095 | TAATAGTTTCATGTG[A/T]ATGTGTGGGTGTAGG | 55130 |
| rs553407561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27974481 | ACCATTTATCGAATA[A/G]GGAGTCTTTTCCCCA | 55130 |
| rs553438303 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27953106 | ATTACTACGATGAAA[C/G]TAATAAATATATCCA | 55130 |
| rs553449553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27935407 | TTGGTAAATAGTAGA[A/G]CTGACGTCTAACCCA | 55130 |
| rs553481586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27848229 | CAAAACAGAGATATA[A/G]ACAAATGAAAGAGAA | 55130 |
| rs553482229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27903016 | GAAAATGTCAAGCCA[A/G]TGTCCCTGATGAACA | 55130 |
| rs553487565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27948901 | CATTAGGTTTTAAAC[A/G]TGCAGAGATTGAATG | 55130 |
| rs553490054 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27880328 | AGTTGAGCTATCTGG[A/T]TGTCTTCTTGAAGTA | 55130 |
| rs553507349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27941249 | AACACTTTAGGAGCT[C/T]GAGGTGGGAGGATCA | 55130 |
| rs553524698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27834343 | CAAAGGCGCTATCCC[C/T]TGGCCTTCTGGAATA | 55130 |
| rs553552188 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27813997 | ATGGTAATCTCACAT[C/T]ATACATAAATAGCAA | 55130 |
| rs553578227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27934567 | TAAGGAGCAACACCA[C/T]TACTTAAAATTCTTG | 55130 |
| rs553590243 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27946451 | GATATTCTGATGCAT[A/G]TATAAAATGTGTAGT | 55130 |
| rs553603133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27954456 | CATATCATGCTCTAG[C/T]TGTGCTGGCTTATAG | 55130 |
| rs553623329 | snp | C/T | 3.29772e-05 | 0.00406048 | missense | ARMC4 | GRCh38.p7 | 10:27860803 | CCCCACATACAGCAA[C/T]GTGAAATAGCTTCTG | 55130 |
| rs553623648 | snp | C/G | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27982370 | CTTAGATATCTCCAT[C/G]CTAAATAAGTTATAT | 55130 |
| rs553626011 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27888628 | TTGTCTATTTATTCC[C/G]TTAATTATTACTTTG | 55130 |
| rs553630647 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27946743 | TACAAGCTTCCCACA[C/T]ACCTCCTCCTTCTTA | 55130 |
| rs553649968 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27948072 | CCATTTAATTGCAGC[A/G]GATGTCCCAAAGGTA | 55130 |
| rs553668959 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27989209 | AAGCCATTAGGTTTG[G/T]GGCAATGTGTTACAG | 55130 |
| rs553703952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27982017 | ACACTCTGTTCTTCT[A/G]TCTGTGGCATGGTTG | 55130 |
| rs553731413 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27913404 | TTTCTATCCCTGCAT[G/T]AATTTGCTTAGGATA | 55130 |
| rs553732923 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27913378 | ATAAGTGAGAACATG[C/T]GGTATTTGGTTTTCT | 55130 |
| rs553737845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27913838 | TCAAAAAATAACAGA[C/T]GCTGGCAAGGTTGTG | 55130 |
| rs553738773 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27992813 | CAGCCCACCTAACTA[A/G]GGGTCAGATGTGATC | 55130 |
| rs553744596 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27822022 | AAATAACTTTTTACA[A/G]CACTGGAGTGAACAA | 55130 |
| rs553763639 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27818947 | TCTGTACTCTGACTC[A/T]CCCAGTCACTGGGCA | 55130 |
| rs553798011 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27909538 | AAGAAGACTCAGGGG[C/T]GGGGCCCAGTGACTC | 55130 |
| rs553802290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27826009 | GACCTCCTCAACTCC[A/G]TTGATCTTCACTTCA | 55130 |
| rs553805034 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27833860 | GGTAAAGGTACACCT[C/T]CCTGAAGAACAAGAG | 55130 |
| rs553832539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27867359 | ATGGTGCTGGGGTGT[C/T]CTGTTAGGCCTGAGT | 55130 |
| rs553855077 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27912651 | ATGTTTTCTAAAAAC[G/T]TCACAGTATTTGGTG | 55130 |
| rs553862238 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27838157 | CAAGCACTGTTTACT[C/T]TTTGTATTTAACAGG | 55130 |
| rs553865098 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27883407 | AAACAGCAACAAATA[C/T]AGGCCACGGGAAGGG | 55130 |
| rs553870331 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27879487 | ATGTCTTTCCTGCTT[A/G]TACTCAGTAACCCAC | 55130 |
| rs553889092 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27906478 | AGGATCTAGAACCAC[A/G]AATACCATTTTACCT | 55130 |
| rs553906145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27925761 | GAGAGACACTAGAGG[C/T]ATCCCCACTAAAATT | 55130 |
| rs553910529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27888070 | CAACGAAGAAAAGGA[C/T]ACTTAAGGTGATTCT | 55130 |
| rs553914586 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27981231 | GAGACGAAAAAGACT[A/T]GGAAATTGACAATAG | 55130 |
| rs553928513 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27956937 | TTCCAAACAAAATAT[A/C]CTACATCCCTTCTCC | 55130 |
| rs553938287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27927777 | ATGCCTGTTTCTTTA[C/T]AGAGACTTTTTCTTC | 55130 |
| rs553987293 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27896390 | TTTCTCACTTCTGGA[C/T]TGAAATTCAAAGATA | 55130 |
| rs553997359 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27963258 | GTGATCCTCCCGTCT[C/T]GGCCTCCCAAAGTGC | 55130 |
| rs554007639 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27830975 | CCTTTTTCCTTTGTT[A/C]TATCAGGTAGAGATA | 55130 |
| rs554053230 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27936988 | CTTCTTTCTAGAGAG[A/C]TCATTTTCGAAAGAT | 55130 |
| rs554065558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27925059 | AGATTTTATAAAAAG[C/T]CAGAAAAAGAAAACA | 55130 |
| rs554067173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27964792 | TTTCTGCGTTTTCTT[A/G]TAGTGTCTTAGTAAG | 55130 |
| rs554082231 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27988608 | CTCCCAAAGTACTGG[A/G]ATTACAGGCGTGAGC | 55130 |
| rs554102235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27868613 | ACGTGTTCTCACTCA[C/T]AAGTGGGAGCTGAAC | 55130 |
| rs554110997 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27906008 | CAACAAAAGCCAGAA[C/T]TGACAAATGGGATTG | 55130 |
| rs554115182 | snp | C/G | 1.64917e-05 | 0.00287151 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27812580 | TACAACCAGCTGCAG[C/G]TTCCTGGAGATCCTG | 55130 |
| rs554120800 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27901004 | AACAACCCCAAGACA[C/T]ATAATCATCAGATTC | 55130 |
| rs554133622 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27844658 | AAGTTTCCAACTCAA[A/T]AGGTTATGGAGAAGA | 55130 |
| rs554156608 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27901291 | CACCACTAGGACTGC[C/T]TTATGAGAGCTCCTG | 55130 |
| rs554156683 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27965102 | TGGGGTTTCAGGTTT[C/T]TCAAGATGATGATGG | 55130 |
| rs554171699 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27962104 | AAAGGAACTGCATGA[A/G]GTGAATAAACCTGTC | 55130 |
| rs554183923 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27899483 | GTTCACACTCCTGGA[A/T]AGGAGGCTGAAGCCA | 55130 |
| rs554198676 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27857543 | TTTCTTAAAGTGTGA[A/C]TGCTAGAAAATTTAA | 55130 |
| rs554212856 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27835008 | AGGTCACCCAGGCCC[A/G]ACAGAACACACAACC | 55130 |
| rs554215986 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27995644 | TGTTATCCCGACTTT[C/G]TTACAGTGACAATAT | 55130 |
| rs554263132 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27821236 | AATATTTGAGAAGTA[A/C]CCCCAAGACCCTCTT | 55130 |
| rs554264213 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27888382 | TGGAGTAAGATGATA[G/T]CTCACTGTGGTTTTT | 55130 |
| rs554276491 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27911687 | AGGTCTACAACAAAA[C/T]CTCTTTCGCAAATTC | 55130 |
| rs554283727 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27950893 | AATGAGCTGAATAAT[A/T]ATGATAATTAATTAA | 55130 |
| rs554294331 | snp | A/G | 0.00066496 | 0.0182219 | intron-variant | ARMC4 | GRCh38.p7 | 10:27935272 | GTTCATCATAAGAAA[A/G]AGGAGAATTGGTTTT | 55130 |
| rs554310865 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27923696 | CTCACACCTGTAATC[C/T]CAGTGCTTTGAGAAG | 55130 |
| rs554318670 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | ARMC4 | GRCh38.p7 | 10:27968588 | GGCTCAGACAGATAC[A/G]TAACTTTGCCAGGAC | 55130 |
| rs554318675 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27845665 | CATTAGTGTGCTGTA[C/T]TCGGGAGACCCATCT | 55130 |
| rs554338258 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872509 | GTCATAAATAGCTCT[C/T]ATTATTTTGAGATAC | 55130 |
| rs554350407 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:28000891 | TCACTCCCTGAAGGA[C/T]TTATCATGACTTGTT | 55130 |
| rs554357492 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27928574 | ATGCCCTCAAACCTC[C/T]TTTACTGCAGGTGAG | 55130 |
| rs554357702 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27967432 | AGAGGCATAGGTGGA[A/G]CATGAACTCCCACTA | 55130 |
| rs554370501 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27832373 | CCTTTAGCTTCTTCA[A/G]TAAGATTATTCCTAG | 55130 |
| rs554375151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27878445 | TCTCTTGCCTCCAGC[A/G]AAAAGCACTGGCAGT | 55130 |
| rs554375262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27871963 | GTATGGCCATTTTCA[C/T]GATATTGATTCTTCC | 55130 |
| rs554376825 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997598 | TTTGAATCTATTCAA[A/G]TTGTATTTCCAAGTC | 55130 |
| rs554394143 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27921253 | TGACCCCTCATCATG[C/T]CACTGTACTTTAGCC | 55130 |
| rs554409183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27838506 | AGACTGACTGCACTC[C/T]AAGTAACCAAACAAT | 55130 |
| rs554419051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27941301 | CCAGCCTGAACAACA[C/T]AGCAAGATCCTGTTT | 55130 |
| rs554456027 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27934671 | AGGCTACTATGAGAA[G/T]GTACCTGACACTCTC | 55130 |
| rs554467158 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27979816 | ATAAATTCAATGAAA[A/T]CTCTATCAAAACCCA | 55130 |
| rs554491271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27886552 | GGATTCTACACAGTA[A/G]CTTGAAGCCATACAA | 55130 |
| rs554496276 | snp | A/G | | | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27981842 | ACCTCCTATATGCAT[A/G]TAAGGCACTCTGCTG | 55130 |
| rs554509511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27875174 | CTTGTGCATTCGTCA[C/T]GTAGTTCTTGTGCCA | 55130 |
| rs554513476 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27921763 | ATCAAGTAATTTACA[A/C]AGGCAAAATAATTAG | 55130 |
| rs554518111 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27845703 | AGAGACACACATAGG[A/C]TCAAAATAAAGGTAT | 55130 |
| rs554549226 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27847520 | CTGGCACAAGACAGG[G/T]ATGCCCTCTCTCACC | 55130 |
| rs554568404 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27820288 | CAAAATCTAGCCTGC[A/G]TTTCGCCCATCCTCC | 55130 |
| rs554574998 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27955112 | ATGTTTCTCAGGAAC[A/G]TGGTACTCATTTGCC | 55130 |
| rs554582469 | snp | A/G | 1.6483e-05 | 0.00287076 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27940614 | AATTAGCATGTTTTC[A/G]TGAGAAGTCTTCAGC | 55130 |
| rs554598280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27829385 | TTTTTTCAAACTCCC[A/G]TTGACTTAACCTCAT | 55130 |
| rs554610103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27914561 | TAGAGCTCAATTACA[A/G]TTTCTCCATAAAGGC | 55130 |
| rs554662870 | snp | A/G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27843991 | GATTGCTTGAGGCTG[A/G/T]GTTCAAGACTGACCT | 55130 |
| rs554665257 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27839756 | ATCCCCAAACCAACA[G/T]GGGAATGCTTCACAG | 55130 |
| rs554667794 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27920653 | AAATGTGAGAGGAAA[G/T]AAAAATGTTCTTGTT | 55130 |
| rs554687627 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27921778 | AAGGCAAAATAATTA[A/G]ACAAGCATCAGACTT | 55130 |
| rs554701895 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27927813 | CCTTAATGATTGAGT[A/T]CATTCTCCTTAAATG | 55130 |
| rs554709597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27911847 | ATGACAGCAGGAATT[C/T]TGTATTTCCCACCAC | 55130 |
| rs554714686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27947281 | TCTTTTAAAAAAACA[A/G]AAGTCAGATATTTTA | 55130 |
| rs554729143 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27888304 | AGTGTTCCCTTTTCT[C/T]CTCACCCTTGCCAAC | 55130 |
| rs554730192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27974557 | GTGCAGCCTTGTTTC[C/T]GGGCTCTCTATTCTG | 55130 |
| rs554738572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27896974 | CCAACTTAAACTCTC[A/G]CCTCTCAGTGGAAAT | 55130 |
| rs554775998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27954240 | ACTGGGAACCAGCCA[A/G]TACCACTACTCTTCT | 55130 |
| rs554778174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27889742 | CTGCAATTATGCATT[C/T]TCACAGTAGAACAGT | 55130 |
| rs554813202 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27888980 | AGAAAACATCCAAAG[A/C]ACAATGTAGCTGAAG | 55130 |
| rs554862683 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27996423 | GAGTATAGAAATATT[A/G]TAGAGATGTCTAGTT | 55130 |
| rs554879068 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27887847 | TTAGATTTTAAAAAA[C/G]TGGGAAGACCCAAAT | 55130 |
| rs554898823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27833601 | CATTTGAAGAGTATT[C/T]TGATATTAGGATATT | 55130 |
| rs554917844 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27887087 | AAATGGATTTTAAAA[A/G]AACAATTCTACAATA | 55130 |
| rs554925017 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27866704 | GAAAGGAAGCAAGAG[A/C]GGGGAGGGAGGTGCC | 55130 |
| rs554927357 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27901337 | TTGGAAAGGAAAAAC[A/C]GGGACCAGCCACTGC | 55130 |
| rs554943124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27989772 | AGGATCACTTGAGCC[C/T]GGGAGGCGGGAGGAT | 55130 |
| rs554946884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27982143 | TTTTCTTCCCTACCT[C/T]TATTGTTCTTCCATA | 55130 |
| rs554950942 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27896456 | GATTGATAGGTAATA[G/T]ATGGATGATTGATTG | 55130 |
| rs554954522 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27895101 | GTGCTAAAATTACAG[C/G]TGATTTTTTTAATTT | 55130 |
| rs554954689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27886680 | TAAAAGACAAATGCA[C/T]AAAAATTATGCATGT | 55130 |
| rs554957301 | snp | G/T | 1.64811e-05 | 0.00287059 | missense | ARMC4 | GRCh38.p7 | 10:27860689 | GAGAGTTGGTACAAG[G/T]CCTGAGCTGTCGCCC | 55130 |
| rs554969623 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27988647 | CTGGCCTGATCTAAC[A/G]TATTTTGAATTGCAA | 55130 |
| rs554989730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27926651 | TTGCAACTTTTCCAT[A/G]AGTCCAATGCTATTT | 55130 |
| rs555007591 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27989268 | TATGAGTCCGATTCT[G/T]CTGGGTGCAGATAGG | 55130 |
| rs555007807 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27916079 | TGGTGCAACCCAACG[C/T]GGGAAGTCAGAACCC | 55130 |
| rs555037627 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27978036 | ATTGAAACTATATGA[G/T]CATACAAATCCTTGT | 55130 |
| rs555084905 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27906600 | TCACAATAGCAAAGA[C/T]TTGGAACCAACCAAA | 55130 |
| rs555085973 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27987771 | GATATAACCAAGGAA[G/T]AATTTTTTTTTTTTT | 55130 |
| rs555092034 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27894346 | TACACATAACCTCCA[C/T]GGATATACATTTACA | 55130 |
| rs555108703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27994419 | GTACCCCATACATTT[A/G]TAGAAATAAAATTCA | 55130 |
| rs555149261 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27987297 | TCTTTTTCAAGAGAC[A/G/T]CTAACAAATGATCCT | 55130 |
| rs555159289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27866910 | GAGGGGAAAATATCC[A/G]AACTATCTCAATGAT | 55130 |
| rs555185822 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27893734 | GGGCAGTGACGGGGA[C/G]AAAGAAAGGGCTATA | 55130 |
| rs555188816 | snp | G/T | 0.0325976 | 0.123435 | intron-variant | ARMC4 | GRCh38.p7 | 10:27859060 | TTTTATAGTTTCTTT[G/T]TTTTTTAAGACTGCA | 55130 |
| rs555189766 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27959365 | GTTGGCAAAGTTCTC[C/T]ACTGCCAGTTCTTTT | 55130 |
| rs555228488 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27959823 | TGAATCATTTTTTGT[A/G]GTAGAGTTATGCTAA | 55130 |
| rs555242882 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27919946 | GTAAAAATAACCCGT[A/G]ATTTAGAACAAAATG | 55130 |
| rs555253214 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27965790 | TGGATTTACAAAAAT[A/T]GAATTAGTGGAATCA | 55130 |
| rs555269800 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27871837 | TTGTCTTGGCAATGC[A/T]GGGTCTTTTTTGGTT | 55130 |
| rs555270114 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27864645 | GAGTGAGGAGTGGGG[G/T]GATAGTGGGCTCTTT | 55130 |
| rs555278916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27878516 | ACATACAAGGCGAGC[A/G]TAACATGACTCAAGA | 55130 |
| rs555286561 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27905862 | ACCTTATACAAAAAT[G/T]AACTCAAGATGGATT | 55130 |
| rs555286973 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27974840 | TTGGGCAGTATGGCC[A/G]TTTGAGTGATATTTA | 55130 |
| rs555295249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27932977 | GAATAAATAAGGAGC[C/T]GGGTGTGGTGGCTCA | 55130 |
| rs555307246 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27871105 | CTTCTCTGATGGCCA[C/G]TGATGATGAGCATTT | 55130 |
| rs555310272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27839436 | CAAACAAAAGCAAAA[A/G]ATGAGGGGTGTTCAC | 55130 |
| rs555323389 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27932089 | ACAGGCGCACACCCT[C/T]ACATCCTTTAATTCT | 55130 |
| rs555325100 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27823540 | TTTTAATAGTACTTT[C/G]CTAATAAGATAGATA | 55130 |
| rs555330302 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27826627 | TCCTCCCATCTGTCA[C/T]GTGGAAGAGGTGTCT | 55130 |
| rs555335341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27825048 | TCAAACCTTATTTCC[C/T]ACAGCCTCCCCTACT | 55130 |
| rs555356799 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27972867 | AAAAACATCAGTAAT[G/T]ATATAGAAGATATGA | 55130 |
| rs555364198 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27857809 | TACTTATGAATAGGC[A/G]ACACGGTGACTCTGG | 55130 |
| rs555376681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27964665 | TTTTTGTCTTTACCT[C/T]GATGTTCAGCAAGAA | 55130 |
| rs555390303 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27850222 | GGCCAAGACGGGTGA[A/G]TCACTTGAGGTCAGG | 55130 |
| rs555401359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27971386 | GAAGATTAATGCCAG[C/T]GGTAAATTCAGGAAA | 55130 |
| rs555415070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27904554 | GCCACTTTTATCATA[C/T]ACTAAATTCCCATTT | 55130 |
| rs555441580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27877578 | ATGACGTCTTGCCTC[A/G]CATAGTTTCTATGGA | 55130 |
| rs555443411 | snp | A/T | 0.0260105 | 0.111035 | intron-variant | ARMC4 | GRCh38.p7 | 10:27846278 | AGAAACTCACTCAAA[A/T]CCGCTCAACTACATG | 55130 |
| rs555443987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27845039 | GCAAGGCAGGCCAAC[A/G]TTCAAATTCAGGAAA | 55130 |
| rs555447440 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27838570 | GCAAAAGGGCCAAGT[A/C]GGAAGGAAAAGACAT | 55130 |
| rs555458267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27850934 | AGTTGAGGAGACAGA[A/G]CTGGAAGTCTGGGAG | 55130 |
| rs555459847 | in-del | -/AAAC | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27971008 | AATAAATAAATAAAT[-/AAAC]AAACAAACAAAATAA | 55130 |
| rs555479763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27945846 | CAGCACTAAAGTAGC[A/G]CATCACACACAAAAG | 55130 |
| rs555491411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27858593 | TAATCTTTCTTATTG[C/T]CTTTCTTTTTCTAAT | 55130 |
| rs555491853 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27985394 | GCTTTTAGGAACTTT[A/C]TTCTACTTCACGAGA | 55130 |
| rs555507204 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27957858 | TTTTTTTTTCCAACA[A/G]TCAGAGACATCACTC | 55130 |
| rs555550625 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27939734 | CAGAGCAAGACCCTA[A/T]CTCTAAAAAAATAAA | 55130 |
| rs555552110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27831278 | GAGGCAACATTTATA[A/G]AATATTAAATCTGTA | 55130 |
| rs555552418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27900151 | CTGTTCTGCAGCCTC[C/T]GCTCATGATACCCAG | 55130 |
| rs555581987 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27844667 | ACTCAATAGGTTATG[C/G]AGAAGATTGAATAAA | 55130 |
| rs555587102 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27852918 | GTGAGCTGAGATCGC[A/G]CCGTTGCACTCCAGC | 55130 |
| rs555631810 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27931200 | GGGGGAAATCTTGAG[A/T]TCTGAAGAGGCATGT | 55130 |
| rs555638928 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27876326 | ACACCCCACACTGCC[A/G]GGTACCCCTCTGAGA | 55130 |
| rs555655613 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27937291 | CTCTTCAATGGCCCC[G/T]GAAATCTAGAGACAA | 55130 |
| rs555657754 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27849391 | GGAACATCACATACC[A/G]GGGCCTGTCGTGGGG | 55130 |
| rs555661527 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27817840 | TGATTTCTTTCCCTT[A/T]AGGTATATATCCAGT | 55130 |
| rs555663039 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:28000004 | CTCGGCTCACCGCAA[C/T]CTCTGCCTCCCATCT | 55130 |
| rs555723100 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27850224 | CCAAGACGGGTGAAT[A/C]ACTTGAGGTCAGGAG | 55130 |
| rs555730966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27824486 | GAATGACCCTTGACA[A/G]ATGCTGGTGCCATGC | 55130 |
| rs555742442 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27914143 | CCATGGAGTACTACA[A/C]AGCCATAAAAAAGAA | 55130 |
| rs555754334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27974392 | TTTTATCCCGCTTGA[A/G]TTGATTTTTGTATAT | 55130 |
| rs555761149 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27916900 | TTCAAGGGACAGCTC[C/T]AGGAAGAAAAAACTA | 55130 |
| rs555822982 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27931725 | AAAAAGTAATGCAAT[G/T]ATAACATTTAGAAGG | 55130 |
| rs555827663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27985340 | AAGCTTTTTCTAAAC[A/G]ACCCAATTAGAATTC | 55130 |
| rs555835563 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27934427 | TATGTATATGTATCT[C/T]TTAATATATGAATAT | 55130 |
| rs555841535 | in-del | -/AAAAAAAAAAAAAAA | 0.396909 | 0.202282 | intron-variant | ARMC4 | GRCh38.p7 | 10:27909818 | GTGAGTCTTCATTTG[-/AAAAAAAAAAAAAAA]AAAAAAAAAAGACTC | 55130 |
| rs555848614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27852919 | TGAGCTGAGATCGCG[C/T]CGTTGCACTCCAGCC | 55130 |
| rs555860327 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27924241 | AATTCTCTGTGTAGT[A/T]AAAAAAAATTTTAAA | 55130 |
| rs555868314 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27884811 | TAAGAACAGCCATGT[A/C]TATGGGGGAAAAAAA | 55130 |
| rs555880996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27980833 | TTTTAGGAAAAGACC[C/T]AAAAGAATTGAAAAT | 55130 |
| rs555891359 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27969998 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAAGCAA | 55130 |
| rs555892965 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27878349 | GGAAAAATATTGAGA[C/G]ATTATTTACAGATTA | 55130 |
| rs555915006 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27840571 | TCAGCTTCCCTTGTC[C/T]GAGATTTTTGAACTG | 55130 |
| rs555942391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27980032 | TAAACTCTTCCATCT[A/G]TGATCAATTGATTTT | 55130 |
| rs555955888 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | ARMC4 | GRCh38.p7 | 10:27847059 | AAAGAGGGAATCCTC[C/T]CTAACTCATTTTATG | 55130 |
| rs555970094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940444 | ATCTTCTCTTTCTCA[C/T]AGAATGCTGACTTCT | 55130 |
| rs555985425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27852107 | ACAAAGACAAAATAA[A/G]AAGTCTTTTTTAGAT | 55130 |
| rs555996341 | in-del | -/AA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27819846 | TTTAAAAAAAAAAAA[-/AA]GGAAAGAAAAAAATA | 55130 |
| rs555999422 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27879255 | TGTGAGGTACCATTG[A/T]GTAACCAGAGGCTTA | 55130 |
| rs556005144 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27849734 | TTGCAAACTTCTCTA[C/T]CATAGAGAAGCAAAG | 55130 |
| rs556005584 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27952720 | TGGTACCTGGGCATA[A/C]GGGTCTTCTGTTTAT | 55130 |
| rs556042155 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27856843 | ATCATGGCGGGTGCC[C/T]GTAATCCCAGCTACT | 55130 |
| rs556047739 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27995481 | AAACCCAAATAGAAA[A/T]CTCCAAGAGTGGAAA | 55130 |
| rs556058602 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27850945 | CAGAGCTGGAAGTCT[A/G]GGAGAACCACAGCCA | 55130 |
| rs556062642 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27858652 | CTAACTGTGTGGGTG[A/G]GCCAAACACAGTTTG | 55130 |
| rs556076172 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997634 | AACCGTAGCAATGCA[C/T]AAGTTTTATTCAAGA | 55130 |
| rs556089542 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27920728 | AACCCTGAAAGGTCA[C/T]GAAGACTTGTTCTGT | 55130 |
| rs556101804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27973678 | CATTTTCTTTATCCA[A/G]TCTCCCACTGATGGC | 55130 |
| rs556102784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27901193 | AATTTTCAACCCAGA[A/G]TTTCATATCCAGCCA | 55130 |
| rs556113774 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27890983 | CACCATGTCATACAG[A/C]GATATATTCGACAGC | 55130 |
| rs556140834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27966281 | GATCAGGTCTATTCA[A/G]GAAGTGACTTAAACT | 55130 |
| rs556143671 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27818908 | TAGTCAAGGGTATGG[C/G]TTTTGAGGTCACAGC | 55130 |
| rs556157367 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27926690 | AATTTAGCAGAAAAT[G/T]TTTTACAAAGAAAGT | 55130 |
| rs556166840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27952228 | TGGCTATTTGACATA[C/T]AAAAAAATTGTCAAC | 55130 |
| rs556181292 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27888879 | AAAGATTACATTTGA[A/C]TTCCTACCTTACACC | 55130 |
| rs556203133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27866697 | GGTAAAAGAAAGGAA[A/G]CAAGAGAGGGGAGGG | 55130 |
| rs556232645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27846394 | AACAAAGACACAACA[C/T]ACCAGAATCTCTGGG | 55130 |
| rs556241714 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872406 | TGTTGAATAGCAGGG[A/G]TGAGAGAGGGCATCC | 55130 |
| rs556252691 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27860992 | CCTAGGTGATGTTTT[C/G]AAGGAACTAGTCTTT | 55130 |
| rs556256119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27918753 | GGAAGTGAACTGTCA[C/T]TATTTGCAGATTATG | 55130 |
| rs556303580 | in-del | -/C | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27994476 | GGCTCATGCCTGTAA[-/C]CCTAGCATTGTAGAA | 55130 |
| rs556318470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27933916 | TACGTGGTTAGACGA[A/G]GCCCCCTGATAGGAT | 55130 |
| rs556332329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27838385 | CAAATAGCTGCCAAT[C/T]AATATAATGGATTTT | 55130 |
| rs556371991 | snp | C/G/T | 9.97119e-05 | 0.00706029 | missense | ARMC4 | GRCh38.p7 | 10:27939914 | GGTAAATGGCCATGG[C/G/T]GCAGTGCTCCTGCAG | 55130 |
| rs556399195 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27831346 | CCAAATCCACCGTTA[C/T]AGACCCAGGAAAGGC | 55130 |
| rs556416045 | snp | A/C | 0.000115355 | 0.00759368 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27812548 | TGTAGCAAGAGCCAG[A/C]CTGCGGATATTGGAT | 55130 |
| rs556427447 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ARMC4 | GRCh38.p7 | 10:27938141 | ATGGGGTTTCACCAC[A/G]TTGGCCAGGCTGGTC | 55130 |
| rs556431249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27946037 | AATTATGTATACAAA[C/T]AGATTATATATATAA | 55130 |
| rs556460780 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27931752 | AAGGAATTTCAAGGT[A/G]GCAACTAGATAACCT | 55130 |
| rs556482704 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27865467 | CAGCTGCCAACTAAG[G/T]TATGCTCTTCTTCAG | 55130 |
| rs556512568 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27845581 | TAGCAATATTAACTT[C/T]AAATGTAAATGGGCT | 55130 |
| rs556537841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27825159 | CCTTATCCAAGCCAT[A/G]AACAAAATTTGTTGG | 55130 |
| rs556538601 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | ARMC4 | GRCh38.p7 | 10:27811994 | TCTCTCTAAGTCCAG[C/T]TGCTTAACTCTAAAT | 55130 |
| rs556540636 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27905957 | AGGACATAGGAATGG[C/G]CTAAGATTTCATGAC | 55130 |
| rs556574738 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27964743 | TTTGTAGCTCAGTAC[C/G]TTGTCCACTTTGGTC | 55130 |
| rs556581144 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27874291 | TACAGCACACTGATG[C/G]GTCTTGACTCTTTAC | 55130 |
| rs556609832 | in-del | -/AA | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27877067 | ATTTGTTGAATTGTG[-/AA]AAAAAAAAAAGGCAG | 55130 |
| rs556614723 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27871912 | TCATTGGTAGTTTCA[G/T]GGAGATGGTATTAAA | 55130 |
| rs556655830 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27848568 | ACAAATGGGATCTAA[A/T]TAAACTAAAGAGCTC | 55130 |
| rs556680061 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27910356 | CCTTCATGGTATTAA[A/G]CCTGCAATTCCAGAG | 55130 |
| rs556680130 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27917084 | AACTACTGCAGAATA[C/T]ACAGTTTTCTCTCAG | 55130 |
| rs556702424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27817740 | TCCAATACTCTATGA[A/G]TGGGCACTTAGGTTG | 55130 |
| rs556735741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27972107 | GAGGGGTTTATGACA[C/T]GTAGAAATAAAATGT | 55130 |
| rs556736986 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27818414 | CTGTCTTGACTCCAT[A/T]GTTATACAAAATATA | 55130 |
| rs556741517 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27909643 | GCCAATGTGGCTAAA[C/T]CCTGTCTCTACTAAA | 55130 |
| rs556764954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27877245 | ACTAATGACTTCCCA[A/G]TTCTCCAGTTGCTTC | 55130 |
| rs556769652 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27998738 | GCCGCCTCTGTTTCC[C/T]GATCCACGCGGGCGG | 55130 |
| rs556786885 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27845083 | ACAAAGATACTCCTC[C/G]AAAAGAGCAACTCCA | 55130 |
| rs556790237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944096 | AGGGCAAGCGATACA[A/G]ACAGAAGGCTCCTGG | 55130 |
| rs556800427 | snp | A/G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27963897 | ACAATCTATGAGGTT[A/G/T]TCATTACTCTCATTA | 55130 |
| rs556804484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27992307 | CAAGGAAAAGTTGTA[C/T]AGTAAATATGACAGA | 55130 |
| rs556817521 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27913706 | TCAAAAGAAGACATA[C/T]ACGTGGCCAGCAAGC | 55130 |
| rs556822596 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27964866 | CCTAGCACAAGGAAG[A/G]CACTCAATAAATATT | 55130 |
| rs556823639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27850264 | AGCCTGGCCAACATG[A/G]TGAAACCCCCTCTCT | 55130 |
| rs556843325 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27928820 | CTACATTTACACACA[G/T]CACTTATTATATGTC | 55130 |
| rs556862492 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27893531 | TTTGCAGCATTACTG[G/T]CAGTGCCATTAATCC | 55130 |
| rs556872429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27883779 | AAGTACAATAACTGA[A/G]ATGAAAAATTCATTA | 55130 |
| rs556881174 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27993071 | CAGAACGTGCCACCA[C/T]GCCCGGCTAATTTCT | 55130 |
| rs556910635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27823021 | ATAGAGAGAGCCCTA[C/T]TGACTTTCTTCTAAA | 55130 |
| rs556934758 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27987044 | CAGCCCTTGTCATCT[C/G]TCTTCTCTATTGACA | 55130 |
| rs556934763 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27978560 | CACTTTGGGAGGCCG[C/T]GACAGGTGGATCACC | 55130 |
| rs556965983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27922743 | AAACCCTGTCTCTAC[C/T]AAAAATACAAAAATT | 55130 |
| rs556975237 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27924192 | ACTCTGATCAAAATG[C/T]AGTATGAGAAATATC | 55130 |
| rs557002869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27915260 | GCTGCAATAACAGAA[C/T]GCCATATGCTGGGTG | 55130 |
| rs557010910 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27875770 | CACCCAGGAAGCACA[A/G]GGGGTCAGGGAATTC | 55130 |
| rs557020785 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27951216 | TATAGATTCATGTAA[A/T]CCAACCAAAATGCCC | 55130 |
| rs557035720 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27850215 | TTTGGGAGGCCAAGA[C/T]GGGTGAATCACTTGA | 55130 |
| rs557040318 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27857599 | TTTCTGCTGGGCAGC[A/G]CTGCTTTACACCTAA | 55130 |
| rs557043988 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27855789 | TCCAATTGAACTGCT[C/T]TCCACTCACTCTGCC | 55130 |
| rs557058895 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27957551 | AAAGGGGGTTCATTG[C/T]TTCCTTTAGAATTAG | 55130 |
| rs557069662 | snp | G/T | | | downstream-variant-500B, intron-variant | ARMC4 | GRCh38.p7 | 10:27811704 | TTTAAAAAGTACTTT[G/T]TGTGCTGAAAACAAG | 55130 |
| rs557070945 | snp | A/G | 1.64939e-05 | 0.0028717 | missense, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984189 | AACATCAAACCTGAG[A/G]TATATTCAATAGATT | 55130 |
| rs557075187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27856954 | CCTGGACGACAAGAC[C/T]GAAACTCCGTCCCAA | 55130 |
| rs557075317 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27864528 | GTGAGGTGAGAGCGG[A/G]GAGTGAGGTGAGAGC | 55130 |
| rs557080375 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27870600 | ATGAGTGAGAATATG[C/T]GGTGTTTGGTTTTTT | 55130 |
| rs557086320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27916023 | GGGGAAACAGTCACA[A/G]GATATTAGAACCTAA | 55130 |
| rs557090190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27969916 | TTTGAGACTAGCCTG[A/G]CCAACATGGCAAAAC | 55130 |
| rs557093090 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27817438 | TGGGCTTTTAATGCA[C/T]CCACCACCCATATAG | 55130 |
| rs557102971 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27899688 | CTCACAGTGTAAACA[A/T]AGCCTCCAGGAAGTT | 55130 |
| rs557112258 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27863677 | AGACTACAAATCCAT[A/G]CAATGAGGAAACCTC | 55130 |
| rs557115377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27823551 | CTTTCCTAATAAGAT[A/G]GATATGGGATTAAAT | 55130 |
| rs557168239 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27926170 | CAAATGCAGCCAAAG[A/G]CAATATATAAATTAA | 55130 |
| rs557181431 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27963514 | TCAAAGTCACAAAGT[C/T]AATGACCATAATAGA | 55130 |
| rs557182212 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27848657 | ATTTTTGCAATCTAC[A/C]CATCTGACGAAGGGC | 55130 |
| rs557210696 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27888324 | CCCTTGCCAACATAC[A/G]TTGTTTTTGTTTGTT | 55130 |
| rs557219638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27876256 | TGCCTCCTCAAGTGG[A/G]TCCCTGACTCCCGAG | 55130 |
| rs557253279 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27952395 | ACTTTTTTTATTTTA[-/T]TTTTTTTTTTTACCT | 55130 |
| rs557261419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27837022 | CAGATCCTAAACTGC[C/T]CACCGTGAGGATTTC | 55130 |
| rs557288389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27897764 | ATCTTTTTCAGGAGG[C/T]TGTCTTTCCTTTAAG | 55130 |
| rs557297089 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27884191 | ATGACTCAAACAAGG[A/G]AACCTCATTAAGCTC | 55130 |
| rs557317607 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27855212 | AAAATTAAAAAAAAA[A/T]TGAAATAAGAAAAGC | 55130 |
| rs557325776 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27842744 | ATTAAAATTCTGAAC[A/C]AACAAAATATTTATC | 55130 |
| rs557333292 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27910991 | ACACCTTATTAAATA[C/T]AGATTGTTGAATCAT | 55130 |
| rs557365654 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27982069 | CTCTGTGTAACGATC[C/T]GTCCACACACCCATG | 55130 |
| rs557396860 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997660 | CAAGAAGGTTGGTGA[G/T]TTTAAGAAAACCTCA | 55130 |
| rs557413779 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27943225 | TCTGGTATTTTTCTT[C/T]TGATGCCAGCTATTG | 55130 |
| rs557459106 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27843391 | GTGTAGTGTACCACC[A/C]AGCATAACTGGGTAA | 55130 |
| rs557475908 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27904959 | TTAAGTCCTTTAACA[C/T]AAATATTGTTTGTGT | 55130 |
| rs557477369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27936116 | CGGGACGTGAATCTC[C/T]TGTTAAAGGAAATAA | 55130 |
| rs557477984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27899602 | TAGCAGTCCAAAGTC[A/G]ACCTGGCATGCTCAA | 55130 |
| rs557484398 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27893585 | GATGCCAAATCCTAT[C/G]ACTCATAAGTTAATA | 55130 |
| rs557495334 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27998099 | ATCACATCGTTAACA[A/C]TTAAACAGAAGCACA | 55130 |
| rs557539415 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999922 | ATTTGTCCTTTGTTT[G/T]GGGTTTTTTGGAGGG | 55130 |
| rs557542781 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27904512 | AATAAATATAAAAAG[C/T]CCATCACTGCCTCTG | 55130 |
| rs557546934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27903421 | CTCTCACCACTGCTA[C/T]TCAATATAGTATTGG | 55130 |
| rs557553591 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27858267 | AGGTTGTTATGCTTC[A/C]CCCATGACCCCACAA | 55130 |
| rs557576421 | snp | A/C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:28000963 | CTGTCACCCAGGCTG[A/C/G]AGTGCAGAGTGCAGT | 55130 |
| rs557586211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27938191 | TTATCCACACACCTC[A/G]GCCTCCCAAAATGCT | 55130 |
| rs557590787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27821767 | CACTTTTTTGGTATC[C/T]ATTTTTTTATCTATA | 55130 |
| rs557611971 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27815396 | AAATTTCTTTAAAGA[A/G]TTGTCTGGAATTCCT | 55130 |
| rs557612931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27986556 | TAAAAAGAGGTTGCC[A/G]TCCTGAGGTTAGCAT | 55130 |
| rs557617027 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27813877 | GGATGGAATAAAAGG[-/T]TAAGGATAGTGAGGA | 55130 |
| rs557622403 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27871083 | CTCATTGTGGTTTTG[A/T]TTTGTACTTCTCTGA | 55130 |
| rs557623486 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997256 | CTGATGTGTATGTGT[G/T]AGACTCTTGAATTTC | 55130 |
| rs557628300 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27864623 | GTGAGAGTGGGGAGT[G/T]AGGGGAGAGTGAGGA | 55130 |
| rs557648669 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27814653 | CATCATGATCTCTTG[A/T]CCATGGGCTCACATA | 55130 |
| rs557650198 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27840388 | CTGAGTTGTCACTTT[C/T]GTGCACATCTTTTGG | 55130 |
| rs557659394 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27870652 | GAATGATGGTTTCCA[G/T]CTTAATCCATGTCCC | 55130 |
| rs557714675 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27958684 | AGCAATAGAAATGAT[A/T]ATTATTGCCAACAGT | 55130 |
| rs557721723 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27987170 | GTGGTAAGGTAGCAG[G/T]CTTTTCATTTTAAAG | 55130 |
| rs557726571 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27970478 | TCCAAGTGTTTTATC[A/C]TCTTTTCTGCATATT | 55130 |
| rs557737922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27957366 | TCCCCTTCACACCAT[C/T]GGGGCAGAGGTAGGG | 55130 |
| rs557759090 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27965212 | GACAGAGGGTTACAC[C/T]AGCCTCATAGGAAAG | 55130 |
| rs557766555 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27916103 | AGAACCCTAGCAGAA[A/T]AAGGGGAATATCCCC | 55130 |
| rs557778090 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27934629 | CAGGTGCTCAAAATA[C/T]ATTTGCTGAATAGGT | 55130 |
| rs557780594 | in-del | -/AAAT | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997719 | ATCAATGTTATTAGA[-/AAAT]AAATAAATAAATAAA | 55130 |
| rs557790227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27977653 | ATGTATCTAACAGAA[C/T]ATATAAGCCAAGAAC | 55130 |
| rs557812004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27979159 | GGTGAAGGTTGCAGC[A/G]AGCCAAGATCATGCC | 55130 |
| rs557836512 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27850841 | GCCCTAAGATTGACC[C/G]AGACTAACTCCAGGG | 55130 |
| rs557839491 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27849698 | TGAGAATTCTTAATT[C/T]CTACTGAAGATAATC | 55130 |
| rs557848110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27857694 | TCCGTCACTGTCAGG[A/G]TAGAATAAACCTTAG | 55130 |
| rs557850519 | snp | C/T | | | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:28000701 | CCAAGATCTGAGCAA[C/T]TATGTCGTTGTTTGC | 55130 |
| rs557867440 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944510 | GAGTATACCTAAAAT[A/C]CTTCCCCAGTTAAGT | 55130 |
| rs557888893 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27861876 | AGCATCCTTCCAGGG[-/T]TTGAATTTCTGCTCT | 55130 |
| rs557893737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27945025 | ATAGAAATGCACTAA[A/G]TAGTTACGAATCCAT | 55130 |
| rs557907793 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27910446 | TAAACACTAAGTACT[A/G]GGCATACAGAAATAA | 55130 |
| rs557909824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27817784 | GCTATTGTGAATAGT[A/G]CCGCAATACACATAC | 55130 |
| rs557935170 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27836453 | ACTTGATCAATGAGA[C/G]AGTTTGGGGACATCT | 55130 |
| rs557978890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27849230 | TGCAGCCACGAAAAA[A/G]GATGAGTTCATGTCC | 55130 |
| rs557997277 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27949712 | TAATTTACAATGATG[A/T]CATTTATAAAAGATC | 55130 |
| rs557998009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27824454 | TACTTGCTTCCACCT[A/G]CTGCCCTTCTGCCAT | 55130 |
| rs558039224 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27957625 | TTGGTGAGTAAAAAT[C/G]TGATACATTCATTAA | 55130 |
| rs558039714 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27830179 | TAATAGGAGTGGAGC[C/T]TAATCCTTGGTCTCC | 55130 |
| rs558048550 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27892184 | CATCACTACAGAGGT[C/T]GAATCTTAGGATCTC | 55130 |
| rs558056790 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984380 | TATCAGGAGAAATAT[A/C]TTTTTTGTAATTAAA | 55130 |
| rs558069644 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27916749 | TATATAACAACAAAA[A/T]ATGTGCTAATTGTTT | 55130 |
| rs558078317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27924023 | AAGAAAGAAAGAAAG[A/G]AGGAAAGAGAAAGAA | 55130 |
| rs558111553 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27822777 | TTTATTGGTGTCTGT[A/C]CTCCTCAAGGTGATA | 55130 |
| rs558131299 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27939459 | GGTGGCTTATGCCTG[C/T]AATCCCAGCACTTTG | 55130 |
| rs558149878 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27912354 | TCAAACTGCCTGGCT[-/G]GCAAAATAACAGCTC | 55130 |
| rs558159655 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27837073 | CTGAAGACAAATTCT[C/G]ATGCAAGAAAGGTCA | 55130 |
| rs558160715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27949291 | AAGCTTATAATGTAG[C/T]GGAGGAAAAAGGTTT | 55130 |
| rs558174282 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27831140 | AAGTCCATCTGCCTT[G/T]TGCTTGGATGCATCC | 55130 |
| rs558175397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27943355 | AACTCCTGAGAGCAA[C/T]TTGTGTGTTTATTTC | 55130 |
| rs558204782 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27844618 | TTATGAAACTCAATT[A/T]CTTTATCTGTAAAAC | 55130 |
| rs558225862 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27866186 | CAACACTGTTTAATC[C/T]TAATTACCCTTTGAG | 55130 |
| rs558237045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27908541 | ATAACCTTTACAAAC[A/G]TGGCTTTGTTTCGGA | 55130 |
| rs558240047 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27850511 | GTAGTGAGCTGATAT[A/C]GTACTACTACACTCT | 55130 |
| rs558249556 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27816341 | TTCAAGAGAAAGGAA[A/G]ATTCTGTTCTGTATG | 55130 |
| rs558266619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27930543 | AGGCTGAGAGAATGG[C/T]GTGAACCCGGGAGGC | 55130 |
| rs558279601 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27922285 | TAACATATAAGAATT[G/T]AGGGAATTCTGCACC | 55130 |
| rs558322878 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27962213 | AATGTCCTAAGCCTG[C/T]GCTTTTCAATAAGAC | 55130 |
| rs558326621 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27870370 | TAATATTATTATTAT[C/T]ACACTTTAAGTTCTA | 55130 |
| rs558352320 | snp | C/G | 2.97446e-05 | 0.00385635 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27985129 | ATCTCTGGTAATTTT[C/G]CCAAGAATATTTAAT | 55130 |
| rs558356971 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27835069 | CGTACTTGTAGACAT[C/T]GCGTGGCCCTGCGTC | 55130 |
| rs558366328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27898720 | TCTGCAAGTTTTTAT[C/T]TTGTTCAACATATTT | 55130 |
| rs558375013 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27943934 | TCTTACCTCCCATGC[A/G]TGTATACTTGGATGC | 55130 |
| rs558404696 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27899099 | ATTTCTGCATTTCCA[A/G]TTGAGGTACCCATCT | 55130 |
| rs558435621 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27921406 | GATATTTTGAAGTAA[C/T]GGAAAATTTAGAGCA | 55130 |
| rs558438496 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27977512 | GTGGAGCTTGCAACG[A/C]GCCAAGATCGATCAT | 55130 |
| rs558439941 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27932123 | CATTTTTTATAGAGA[C/T]GGGGGTCTTGCTATG | 55130 |
| rs558447844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27863052 | AAGCCTCTGGCTACA[A/G]CATTTTCATCAGTTG | 55130 |
| rs558466954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27816208 | CACCCTGTCTTGTCC[C/T]TGTCTGATGAACTAT | 55130 |
| rs558486762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27869787 | TGATCCACCTGCCTC[A/G]GCCTCCCAAAGAGCT | 55130 |
| rs558493695 | in-del | -/TTTT | 0.00202552 | 0.0317594 | intron-variant | ARMC4 | GRCh38.p7 | 10:27937943 | ATTCATATATAGAGG[-/TTTT]TTGTTTTTTGTTTTT | 55130 |
| rs558510155 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27859971 | TATGGTTGCCTCTAT[A/C]CTTTATTATTTATGT | 55130 |
| rs558525265 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27834013 | TGCAGTGTGTGCAGC[A/T]CCAAGGTGCTGGCCA | 55130 |
| rs558529154 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27994186 | GAAGTAAATTTTTTT[G/T]CATCTCAGATTTGAA | 55130 |
| rs558530645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27909068 | ACAATGAAGGATTTG[C/T]TTTTCAAATTTAAAT | 55130 |
| rs558537314 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27842198 | GTAATTATTTTGTCC[A/C]TTTACATGTTTTTGA | 55130 |
| rs558555708 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27935343 | CCTTACAACAACCCA[A/G]TGATACAGATATTAT | 55130 |
| rs558576572 | snp | C/G | | | missense | ARMC4 | GRCh38.p7 | 10:27940799 | GTGCACAGTCTAGTA[C/G]AGCAACCTATAATAA | 55130 |
| rs558585552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27848146 | AGAACAAAGCCGGAG[A/G]CATCACACTACCTGA | 55130 |
| rs558593711 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27903116 | ACGATCAAGTCAGCT[A/T]CATCCCTGGGATGCA | 55130 |
| rs558597340 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27998151 | CGGAAAGGCAGCCAT[C/G]AGCTCTGAGATCTAT | 55130 |
| rs558633962 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27884886 | AGACCCAAGAAGACC[-/T]TCTGCTTTTACTCTG | 55130 |
| rs558643402 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27867805 | AATACAAAAATTAGC[C/T]GGGCATGGTGGCGTG | 55130 |
| rs558657445 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27835945 | AAAAAAAAAGGAAAA[C/G]AAAATCATAAGGAAG | 55130 |
| rs558694086 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27885183 | AATAAATAAGGAAAA[A/T]TATATATAAACAAAA | 55130 |
| rs558708526 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27835618 | TAACAATAACATAAA[C/G]AGTCGATCAACACCT | 55130 |
| rs558712776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27968698 | TTCTTTTCCCACAGT[C/T]AACTAATACTAGTAA | 55130 |
| rs558729157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27941913 | AGTCTTTCAATCCCA[A/G]TTCCAAGTTCCTGGG | 55130 |
| rs558733772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27907109 | TAAGAGAAATAGGCT[C/T]AAAAGTGATCTTCAA | 55130 |
| rs558745147 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27843190 | ATAGTTTATTTTTTT[A/T]AAAAATAAGCTGAAG | 55130 |
| rs558751149 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27973561 | CTCATCATTTAGCTC[C/T]CATTTATAAGTGGAA | 55130 |
| rs558755083 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27881974 | AGTTCGAGACCAGAC[G/T]CGACAACATGGTGAA | 55130 |
| rs558789819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27881336 | CAAACATTGTACTGT[A/G]TATTCAATGCCACTT | 55130 |
| rs558823478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27813927 | ATTTGGGATGAAATA[A/G]CTCTTCAATAAATGG | 55130 |
| rs558835929 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27935949 | TTTCTATACAGAACA[G/T]TTTCCCTTCCTAATA | 55130 |
| rs558854078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27880171 | ATACAGGCCAGGACT[C/T]CCCTGTCCTGCCCTT | 55130 |
| rs558854845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27913264 | TGATAGGTAGTTTTT[C/T]GATCCTCACCCTCCT | 55130 |
| rs558877074 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27848819 | CTCATCATCACTGGC[C/G]ATCAGAGAAATGCAA | 55130 |
| rs558878535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27960587 | ACTCCTGACCTCAGA[C/T]GATCCACCCTCCTCG | 55130 |
| rs558940936 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27967162 | ATCTCAATCAAGACC[A/G]CACATAACAGCGTGG | 55130 |
| rs558976728 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27947446 | CTCCAGCATGGGCAA[C/G]AGAGTGAGACCCTGT | 55130 |
| rs558981775 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27873832 | AAGAATGCATATTCT[C/G]TTGATTTGGGGTGGA | 55130 |
| rs558987967 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27942166 | TTTGGAATTGCATGG[G/T]GGTTAGCAGGTGCTC | 55130 |
| rs559018580 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27941368 | TGCATGTGTGTAGTC[C/T]CAGCTACTCAGGAGG | 55130 |
| rs559023558 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27920306 | TAAAAAAATTTTAAA[G/T]GCTTTTTATTTTATT | 55130 |
| rs559026045 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27942938 | TTTTGGAAAATTTCT[G/T]AACACATTTTTCAGT | 55130 |
| rs559040571 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27854518 | CCCAACACTTTGGGA[G/T]GATGAGGTGGGCAGA | 55130 |
| rs559061201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27954967 | TTTTAGCTGATGGAA[C/T]TTAAATATGTTATGA | 55130 |
| rs559091535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27976678 | CATTTTTCCTAAATT[C/T]GTCTATAAATTCAAG | 55130 |
| rs559094048 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27917087 | TACTGCAGAATACAC[A/C]GTTTTCTCTCAGTGC | 55130 |
| rs559117157 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27814950 | CAAAATTTGTGTCCC[A/T]CTCATTAGGTTACTT | 55130 |
| rs559118381 | snp | A/T | 3.29609e-05 | 0.00405948 | missense | ARMC4 | GRCh38.p7 | 10:27860717 | CCCGATGCACGTTGG[A/T]GTCATTTGATTTCAG | 55130 |
| rs559118582 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27996324 | ATTTTACATTCTGTA[A/C]TGTATTAAATCTTTG | 55130 |
| rs559125507 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27936407 | TTCCATGGGAAATCC[A/G]CCCACTCACCTTGAT | 55130 |
| rs559158644 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27821472 | ATATGTTTTCATTTT[C/T]CTACGAGCCTCACAA | 55130 |
| rs559158779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27948332 | TGTCACTGACCACAC[C/T]CCCAAAGGGATTATA | 55130 |
| rs559197222 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27820829 | CTCCTGTTGCCCAGG[A/C]TAGAGTGTAATGGTG | 55130 |
| rs559198850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27919767 | GACTCAGAAATTCCA[A/G]TGCAAGGATATGCAA | 55130 |
| rs559213781 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27854825 | CATACAACGGACTAC[C/G]ACTCAGAGATAAAAG | 55130 |
| rs559223145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27954325 | ACAAAAATAAGTGTT[A/G]TTGCAAATACATGGG | 55130 |
| rs559223833 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27891463 | GTTACAAGGCCAAAT[A/G]ATCTCATGGATATAT | 55130 |
| rs559232452 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27911645 | TTCCCAGCCATCTCC[A/G]TATTTTACATAGTAA | 55130 |
| rs559235729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872978 | TCGGCTATGAATCCC[C/T]CTGATCCTGGACTTA | 55130 |
| rs559243665 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27943575 | GCGGATTACCTGAGC[G/T]CAGGAGTTCAAGACC | 55130 |
| rs559244940 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ARMC4 | GRCh38.p7 | 10:27846140 | TCTCAGCACCACATC[A/G]TACTTATTCCAAAAT | 55130 |
| rs559249838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27834248 | TGGCGTAACATTATA[C/T]GTGCATGTGGTCTAG | 55130 |
| rs559279499 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27920856 | ATAAACCCAATGTAA[A/T]AACTGAAAAAAAAAA | 55130 |
| rs559283280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27955158 | GTTGATTCGAGTGGA[C/T]GAACAGTGAGCATTG | 55130 |
| rs559285549 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27902688 | TACACAAATAAACTA[G/T]AAAATCGAGAAGAAA | 55130 |
| rs559288714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27909100 | GAAAAGTCATACTGC[C/T]TTCCATATGCTACTT | 55130 |
| rs559341010 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27952727 | TGGGCATAAGGGTCT[C/T]CTGTTTATTTGCTCC | 55130 |
| rs559376963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27891280 | TCACAGAAATTAACT[C/T]CTCTTCTCTTTTGGG | 55130 |
| rs559393468 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27855390 | TACTCTATATGTAGT[A/C]TATATTCATCGATAC | 55130 |
| rs559398914 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27828633 | GTTCATAATTTAACA[A/C]GGAAATATTTTTAAA | 55130 |
| rs559436799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27903181 | ATCCATCACATAAAC[A/G]GAACCAGTGACAAAA | 55130 |
| rs559483116 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997806 | CCAGTTGCTCCCCGG[C/T]TTCTGCCCATTGCCA | 55130 |
| rs559502823 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27880714 | CATCTTGGAAGCAGA[C/G]AGCAGCCCTCACCAG | 55130 |
| rs559521708 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27990898 | GAGTGAGATTTAAAA[A/C]TAAAATATGGCAATA | 55130 |
| rs559534610 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27955862 | GAGAAGAAACCCAAA[A/T]CCTGCCAGGGAGGAG | 55130 |
| rs559535845 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27834633 | GGCAGGCAGGGGGCA[G/T]ATCGTGAAAGGGCTT | 55130 |
| rs559543946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997405 | AACATTTGTTTTGGT[A/G]ATCTTATAAAGATTG | 55130 |
| rs559545542 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27896054 | CGTTCACTAGACAAG[G/T]GTCTTCAACATTTTG | 55130 |
| rs559560035 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27888816 | AATGGGGAAAGTCTT[C/T]TCAAAAATGTTGTTG | 55130 |
| rs559576750 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983821 | CCACTGGCTTTAGTT[A/G]CGTTTTTAAAAATTT | 55130 |
| rs559577936 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27965897 | TCAACATTAAACTCA[C/T]GGGCAAGGACTAGTC | 55130 |
| rs559603498 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27899808 | AAAGAAAGGAAGCAG[C/T]TCCAGTCAGGAGCTT | 55130 |
| rs559609919 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27928252 | CCAAGCCAGCAAACC[A/G]AACATCATCTACGAC | 55130 |
| rs559612823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27995868 | TATATCCTGCCCAGA[C/T]GACATTTTACTGTAA | 55130 |
| rs559647883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27979878 | CCTAAAATTCATAAA[C/T]AGTGTCAAGGAATAC | 55130 |
| rs559650756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27996467 | GAAAGGGGGCATTAT[C/T]GGCCTTTAGTGTTGA | 55130 |
| rs559661744 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27989401 | AATGACATGCATTGT[G/T]CACAAAATGTATATT | 55130 |
| rs559675634 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27881508 | TGGGCATAGTGGCAC[A/G]CACCTGTAGTCCCAC | 55130 |
| rs559687124 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27867669 | TACAAATAAGCAAGG[C/G]CTGGGTGCAGTGGCT | 55130 |
| rs559720673 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27960959 | CCTTGCCCTCCTGCA[A/G]ATTCAAATACTTAAA | 55130 |
| rs559722361 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27867207 | AGGCAGAGGCATTTG[G/T]GAAGGTCTTGAGAGC | 55130 |
| rs559726112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27874795 | CCTTAACATTTTTTC[C/T]TTCATTTCAACTTTG | 55130 |
| rs559726225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27868335 | ATTACTTGGGTATAT[A/G]CCCAAAGGAATATAA | 55130 |
| rs559746044 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27982997 | CCGTCATTAGAATCA[C/G]CTAAAGGAAGACTGA | 55130 |
| rs559755359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27813556 | AGATTTTTTAAAAGT[A/G]AATTTGAATCACATA | 55130 |
| rs559768659 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARMC4 | GRCh38.p7 | 10:27967620 | TTTAGGCCAGGTGCA[A/G]TGGCTCACATCTGTA | 55130 |
| rs559776688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27966363 | TGAGGAAAGCCTAAA[C/T]TCACCTTCCTTAGTC | 55130 |
| rs559787605 | snp | A/C/T | 0.000548396 | 0.0165498 | intron-variant, missense | ARMC4 | GRCh38.p7 | 10:27853315 | GAGGTTGCAGTGAGC[A/C/T]AAGATCGTTGTCACT | 55130 |
| rs559807150 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27869202 | AATGGATAATCTTTG[C/T]CAATAGAAGATGTGA | 55130 |
| rs559809464 | snp | G/T | 0.0121911 | 0.0771164 | intron-variant | ARMC4 | GRCh38.p7 | 10:27968879 | CAGTAGCCCACTGCG[G/T]GAGGGTGGCTTTAGG | 55130 |
| rs559818896 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27924000 | AGAAAGAAAGAAAGA[A/G]AGAAAGAAAGAAAGA | 55130 |
| rs559832032 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27840142 | TTTCACAACTGAGGT[A/G]AAATATTCTACAAGT | 55130 |
| rs559856856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27885294 | AGGTGGGCAGATCAC[A/G]AGATCAAGAGATCGA | 55130 |
| rs559858662 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27913001 | TTGGGATAAGTATGT[C/G]AGAAATTCTTTAGCC | 55130 |
| rs559870415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27841691 | ATGAGCCACCACCCC[A/G]GCAGATCTGCTTCCA | 55130 |
| rs559893170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27906855 | ACATCACACATCGGG[A/G]CCTGTCAGGGGGTGC | 55130 |
| rs559898543 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27973173 | AGTTTATACAATGCT[C/G]ATAAAGAAATTTGCA | 55130 |
| rs559901527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27847634 | AGGAAGTCAAATTGT[C/T]CCTGTTTGCAGATGA | 55130 |
| rs559921613 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27941533 | AGATCTCTTTGGAGG[A/G]CATAGCCTGCCTCAT | 55130 |
| rs559933159 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27998296 | GGCCCTAAGTAAAAC[C/G]AAAGCTAAGCCTAGT | 55130 |
| rs559936708 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27934212 | GAATTAAACCTCTTT[A/C]CTTTATAATTACCCA | 55130 |
| rs559939614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27965898 | CAACATTAAACTCAC[A/G]GGCAAGGACTAGTCC | 55130 |
| rs559992085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27846750 | AGGGGATATCACCAC[C/T]GATCCCACAGAAATA | 55130 |
| rs560057884 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27906249 | TATGCGACCAACAAA[C/T]GTATGAAAAAAAGCT | 55130 |
| rs560061882 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27946943 | ATGTCCTCAACAACT[C/G]TCCCGTGAAGATGTC | 55130 |
| rs560084524 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27950331 | AGTGGTGTATAACCA[C/T]GTGAGTCAAAGCAGA | 55130 |
| rs560089681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27813073 | CTCAGTGCCAACTAA[C/T]TAGAGCTGATCTATT | 55130 |
| rs560091396 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940881 | TTCAATAGCTACAGT[A/G]TTCCTTACCAAGCTC | 55130 |
| rs560099198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27947720 | GAGAGTTATTTAGGC[A/G]GAGGCTTCAGACTTC | 55130 |
| rs560106735 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27962361 | TCAATGGCCCACGTG[C/T]CTCGTGGTTACCACA | 55130 |
| rs560137168 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27839716 | AGATATAACATATAA[A/G]GATGTATAATTTGCC | 55130 |
| rs560152252 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27959476 | GAGGCACTGTTGCAA[C/G]CGTGGCCTAAATGTC | 55130 |
| rs560203128 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27850575 | AAATAAATAAACATC[C/T]ACATAAATAAATAAA | 55130 |
| rs560206645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27933293 | GAATGTAACTCCAGA[C/T]AATTGATATTTGCAA | 55130 |
| rs560210819 | in-del | -/C | 0.00438332 | 0.0466095 | intron-variant | ARMC4 | GRCh38.p7 | 10:27998471 | GGCGGAGGAGAAAGA[-/C]CGGGCTGGGGGAAGG | 55130 |
| rs560216923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27945353 | TCCTACAGATGTGCA[C/T]AGAACAGTCCGGAAT | 55130 |
| rs560233310 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27980104 | TCTTCAACAAATTGT[A/G]CTGGGAAAACTGAAT | 55130 |
| rs560246700 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27963984 | CCCAGCACTTTGGGA[A/G]GCCGAGGTGAGTGGA | 55130 |
| rs560261842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27826385 | GCTCTCCGTGTTGCC[C/T]GGTCATCCACCCAGG | 55130 |
| rs560271206 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27920876 | GAAAAAAAAAAACTA[C/T]GTAAATGCAACATAA | 55130 |
| rs560278309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27919107 | TCAATATCATTAAGA[C/T]TTCCATTTTCCTTAA | 55130 |
| rs560281904 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27930867 | ACAGTCAATCTGGTT[C/T]ACTCTAAATCTCTAA | 55130 |
| rs560309489 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27951540 | GTTGATACAATTGAC[C/T]GTTCCTCTAGAGAAA | 55130 |
| rs560310418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27878097 | TTCACTACTTAGGAG[A/G]TTAGTAATTTTAAAA | 55130 |
| rs560323763 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27849373 | CACTTGGACACAGGA[A/C]GGGGAACATCACATA | 55130 |
| rs560342638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27832576 | TCAATTACTTTGGTA[C/T]AGAACTTTGTCAAAA | 55130 |
| rs560344848 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27886828 | TTGTTATAACTTTAG[A/T]ATGGTAGATGTAAGC | 55130 |
| rs560354919 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27955876 | ACCTGCCAGGGAGGA[-/G]GCTCTGGGAGTCCCT | 55130 |
| rs560372608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27858750 | AATAATTGCGAGTTG[C/T]ATATACACCAGGCAT | 55130 |
| rs560375530 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27932547 | AAGGGAGACAATGAT[A/T]AATTCTATATGGAAA | 55130 |
| rs560381022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27911123 | CTTAGGAACACTGGG[C/T]GGCACTTCAGCACTA | 55130 |
| rs560387916 | snp | A/C/G | 0.00239401 | 0.0345304 | intron-variant | ARMC4 | GRCh38.p7 | 10:27824073 | TGAACCCCAGGGGGC[A/C/G]GAGCCTGCAGTGAGC | 55130 |
| rs560404519 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27924429 | ACTTTTATTATTTTT[A/T]AAAAAATTAAAATAA | 55130 |
| rs560407579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27865750 | AGCCTTAAAAGAAAG[C/T]TTTCACTGTGGTTAC | 55130 |
| rs560417869 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27905510 | TCACAGAATTACAAA[A/C]AACTACTTTAAATTT | 55130 |
| rs560464000 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27938923 | TCTTTTTGGCATACT[C/T]TCTTGATGCTGCACA | 55130 |
| rs560469960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27925514 | AGGTGCACACTACCA[C/T]GCTCAACTAATTTTT | 55130 |
| rs560483828 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27900317 | CCATCTGAAGGTCAC[C/T]AACCTCAAAGACCAA | 55130 |
| rs560484337 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27820948 | CACCACACCGGCTAA[C/T]TTTGCATTTTTAGTA | 55130 |
| rs560508452 | in-del | -/TG | 0.00478085 | 0.0486577 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940183 | ACACATATGTGTGTT[-/TG]TGTGTGTGTGTATAT | 55130 |
| rs560532633 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27827598 | GTCACAAACTCCTCT[C/T]GTTTTTACTTGTCAA | 55130 |
| rs560545603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27979544 | ATTAGATCTGATTTG[A/G]TCACTCAAAAGCTGT | 55130 |
| rs560556615 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27958396 | CCATGTTCACTGGGA[C/G]GATATTATTGAGGCT | 55130 |
| rs560563245 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:28000150 | AGAGACGAAGTTTCA[A/C]CATGTTGGCCAGGTG | 55130 |
| rs560567838 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27890120 | ATGTGTGCAATGAGG[C/G]AACCGAAGATAGCAA | 55130 |
| rs560581822 | snp | C/G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27879407 | ATGTGTGTATATCTA[C/G/T]GCATATGTCTTTTAT | 55130 |
| rs560592674 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27823996 | ATACAAAAAATTAGC[C/T]GGGCGAGGTGGCGGG | 55130 |
| rs560600813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27994628 | CCAGGCATAAAGCAG[C/T]AATGGATGTTGGCAG | 55130 |
| rs560604922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27899723 | CTGGGCGGAGCCCAC[C/T]ACAGCTCCGCAAAGC | 55130 |
| rs560613445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27916282 | AGAGCCTGAATGGGG[C/T]GAAGAGAACATTTTG | 55130 |
| rs560624416 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27980230 | CTTAGAGGAAAAACA[C/G]AGTGCTAAATTTTTC | 55130 |
| rs560633591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27837830 | AGGATAAGCCATTGT[A/G]GTCCATCACTCCTAA | 55130 |
| rs560640176 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27864065 | ATTACAGGGTGCAGG[G/T]TTGGAGTGGGTGCAA | 55130 |
| rs560644668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27860320 | TAGCCAGGTATGGTG[A/G]CATGCACCTGTAGTC | 55130 |
| rs560646281 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27900305 | CACAAAAAATCCCCA[A/T]CTGAAGGTCACCAAC | 55130 |
| rs560661614 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27858016 | TAGCAGTCACACATG[C/T]AGTTGTGACACATTC | 55130 |
| rs560672904 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27996494 | TTGAGGACCGACAAT[A/G]TAAAATATCCTGTGC | 55130 |
| rs560678190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27899066 | AGCTCCCAGTGAGAT[C/T]GACACAGAAAGTGGG | 55130 |
| rs560726101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27902001 | AGATCAACAGAATAT[A/G]CATTCTTCTCAGCAC | 55130 |
| rs560727033 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27817950 | TCTAGATACATACTT[C/T]GCACCATTCACCATT | 55130 |
| rs560733013 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27957939 | CTAGCTTAAATCTAC[A/T]TTTAAGCCATAATTT | 55130 |
| rs560762526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27960191 | ATATTTTTCATTTTG[C/T]ATTGATGTTGGTAAA | 55130 |
| rs560793286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27833938 | TGGGGATTGGGAGAA[C/T]ATTCCAAGCCGAGAA | 55130 |
| rs560799474 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27964346 | TAGTCTTTTAACTTA[C/T]GTGTGCCTCGGTTTC | 55130 |
| rs560826814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27934007 | TGGGAGTTAATTGAA[C/T]CATGGGGGCAGGTCT | 55130 |
| rs560827655 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27827382 | CACACACACACACTA[A/T]ATATATATATATATA | 55130 |
| rs560831017 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27840895 | GTAGGACTTTGGATG[C/G]ATCAGACTGTCGAGC | 55130 |
| rs560849785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27898002 | GAATATGAAAATACT[A/G]AAAAATCTTTTAAGC | 55130 |
| rs560854584 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27865809 | GGTGAAGGCAGGACA[C/T]GAGTCAGGTTCTATG | 55130 |
| rs560855602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27839912 | AAAAGAGTCAACTGT[C/T]ATTCTGTTTAAATTT | 55130 |
| rs560864972 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27814168 | AAAAAAGGGAAACAG[G/T]GACCCTCCGCAAAGC | 55130 |
| rs560894831 | snp | C/T | 0.093417 | 0.194889 | intron-variant | ARMC4 | GRCh38.p7 | 10:27873170 | AGTATTCTCTGATGG[C/T]AGTTTGTATTTCTGT | 55130 |
| rs560899907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27853462 | ACAAATATGATTAAA[A/G]GATATTAAAAGCTAT | 55130 |
| rs560901381 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27813711 | GTGTGGCTTTTACTC[C/T]ATAGGTAATAAAAAG | 55130 |
| rs560909737 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27831989 | TTGCTCCTGCACAAC[A/T]TTGGACTCACAGTCA | 55130 |
| rs560916201 | snp | A/C | | | downstream-variant-500B, intron-variant | ARMC4 | GRCh38.p7 | 10:27812099 | CAAAGCCATAATGAC[A/C]GGACAGTTAGATTGG | 55130 |
| rs560929630 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27822912 | TTCCATGTTTCTTCA[C/T]GAACTTTCCACTAGA | 55130 |
| rs560956949 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27913121 | TTATCATATAGTAAA[C/T]ATGTTTCTCCTTTTT | 55130 |
| rs560977878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27837954 | AGACATTTCAGTAAG[C/T]GACATCTTACCCCAC | 55130 |
| rs560990171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27953845 | AAACACAGAAGGGAG[C/T]AAGGGAAACGGGAAG | 55130 |
| rs560995257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27933343 | AAGTTAAATGGGGCC[A/G]TAAGACAAAATGCTT | 55130 |
| rs561010304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27828424 | TGAGATCACCATTAC[A/G]GAGGATGGGAAAGGC | 55130 |
| rs561021713 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27939605 | TAGCCAGGCATGGTG[A/G]TAAACACCTGAAGTG | 55130 |
| rs561028665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27920527 | GTTTTAAAATGAGAA[A/G]ACCAAGATTCGGAAG | 55130 |
| rs561040807 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27926969 | ACACGTAAATCTACT[C/G/T]TTTCATAAACTTAAT | 55130 |
| rs561051811 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27995950 | CTTTCAGCCTTTTTA[A/T]CTAAATTAGTTATCA | 55130 |
| rs561074033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27873979 | TCTCCCATTATTATT[A/G]TGTGGGAGCCTAAGT | 55130 |
| rs561081939 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27974334 | TGGTATTGCCTAGGT[G/T]GTCTTCCAGGGTTTT | 55130 |
| rs561090984 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27887601 | CAAGTCTTTAAAAAT[-/A]AAAAATATTGAAGTC | 55130 |
| rs561121050 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27832073 | CTTCAGGGGCTAACA[C/G]AGAGGTAACTCAATA | 55130 |
| rs561128981 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27973769 | CATGTGTCTTTATGC[A/G]ATGATTTATATTTCT | 55130 |
| rs561145249 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, intron-variant | ARMC4 | GRCh38.p7 | 10:27812168 | CTATGAAACTGTGCA[C/T]TGGGAAGGCCATATC | 55130 |
| rs561166371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27826638 | GTCATGTGGAAGAGG[C/T]GTCTCCTCCTGCCCA | 55130 |
| rs561169398 | snp | A/G | 0.0486741 | 0.148216 | intron-variant | ARMC4 | GRCh38.p7 | 10:27846847 | GATAAATTCCTGGAC[A/G]CATACACCCTCCCAA | 55130 |
| rs561178307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27818670 | GTAATAGGAGGAGAA[C/T]AGATTGCTAGCTACA | 55130 |
| rs561190488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27943329 | GCAGAAAAATCAGTC[A/G]ATTCAGAGAAAACTC | 55130 |
| rs561200081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27946251 | GTATATTTCTATATA[C/T]AAATAGATAACATAT | 55130 |
| rs561208191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27852611 | GATAGAAAAAGATGA[A/G]TAAAGAGAAAAAGCA | 55130 |
| rs561218493 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27947438 | CTACCACTCTCCAGC[A/G]TGGGCAACAGAGTGA | 55130 |
| rs561221052 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27926081 | TTCTGTAAAGAGCTA[C/G]ATATTATTTTAGTCT | 55130 |
| rs561237364 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27865303 | CACTAAAATATTTGT[A/G]TTTTTAAAAACTCTC | 55130 |
| rs561237894 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27910848 | AGTCAGTGCAAACCT[G/T]TGATGAACAAATAGT | 55130 |
| rs561238097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27918370 | TGGCTCATCCTTCCA[A/G]AACAAATCATGGTGA | 55130 |
| rs561250537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27887557 | ACAATAAACGTTCTC[C/T]AGGATAGACCATATA | 55130 |
| rs561250813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27895905 | TTTGTTGTAGAAGGA[C/T]GCAAGGTGGGAGACA | 55130 |
| rs561257879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27919329 | ATGAACCTTAAAGGA[C/T]AACCGAAAAATTGAC | 55130 |
| rs561265707 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27900878 | GAATGGAACCAACTT[C/G]GAAAACACTCTGCAG | 55130 |
| rs561276813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27911230 | TGCCAAATGGACAAG[C/T]TGTTCACAGTGTGAG | 55130 |
| rs561280520 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27878787 | ATCCTCAAGCACAGA[C/G]AGTTTGTTTGTGTTC | 55130 |
| rs561302744 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27917245 | TCTGGAAAATAACCA[C/G]TTTTAGAAATTAAGC | 55130 |
| rs561324471 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27894942 | AAATGAATTATGATA[A/T]ATCCATACAATATAA | 55130 |
| rs561335097 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27973311 | CCAGCCTGGCCAACA[C/T]GGCAAAACCCCATCT | 55130 |
| rs561356364 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27828532 | CAGGAAGTTGAGGTA[-/T]TTTTCTGGCTTTTAC | 55130 |
| rs561356430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27987546 | GACTGTTGTTTCACT[A/G]AAAAATAAAAATAAA | 55130 |
| rs561358515 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27995204 | GAGCAGAAAGAGAAA[C/G]AGACAACAGCGTCCA | 55130 |
| rs561395203 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27988192 | GATTTTTTTCAGGTT[A/G]GCCTTTAAAAAATAT | 55130 |
| rs561395674 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27972942 | CACCTCTCATTAACA[C/G]CAGAATACAGTCTCC | 55130 |
| rs561400215 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27966357 | GTTCTTTGAGGAAAG[C/G]CTAAATTCACCTTCC | 55130 |
| rs561419557 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27994678 | GATGCCCTGTTAAAA[G/T]AAATTTACCCACAAA | 55130 |
| rs561437582 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27834151 | AGTCCTATGAATGCA[C/T]TGATTTGAGTCCAGG | 55130 |
| rs561448458 | in-del | -/A | 0.00835141 | 0.0640778 | intron-variant | ARMC4 | GRCh38.p7 | 10:27951696 | TTAGAATGGCTTCAG[-/A]AAAAAACCTTCCTAG | 55130 |
| rs561460287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27871994 | TATCCAAGAGCATGG[A/G]ATGTTCTTCCATTTG | 55130 |
| rs561479035 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27932504 | TGTGATATAGTCTAT[C/T]GAGTGATACAAAAAT | 55130 |
| rs561504471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27972262 | TAAGCCAGAGGGCAG[C/T]TAAGAAACTTTTAGT | 55130 |
| rs561516003 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27958426 | TGTTCACTCTCTCAC[C/T]CCGTGCCTGCCCCAT | 55130 |
| rs561530782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27893700 | AAAGCTGAGCCATTA[A/G]CTTACCTAAATAGGA | 55130 |
| rs561569922 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27859078 | TTTTAAGACTGCATA[C/T]TTAGGTTGTGCAAGT | 55130 |
| rs561599824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27865019 | TGATCATTAGAAACC[A/G]TAAATCTGATGATCC | 55130 |
| rs561640059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27992552 | AAAATTGACCAGGCA[C/T]AGTAGTATGTGCCTA | 55130 |
| rs561675787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27993327 | AAGTTACCACTGGCA[C/T]AGTTAGAAATAAAAT | 55130 |
| rs561677761 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27985646 | CTGGGTATTTATAAA[A/G]GCTTTCTTTCCAAAA | 55130 |
| rs561682803 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27964864 | CCCCTAGCACAAGGA[A/G]GGCACTCAATAAATA | 55130 |
| rs561682849 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27958014 | GACATTCAATTTTGC[A/T]TTTCACAGACTTTTA | 55130 |
| rs561700908 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27978050 | ATCATACAAATCCTT[C/G]TACAAAAATGTTCTT | 55130 |
| rs561709615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27899661 | ACTGAGGCTTGAGTA[A/G]GTGGTTTTCCCCTCA | 55130 |
| rs561711575 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27817313 | TGATCTCTTTGTTTA[C/T]ACCTCACTTTACTGT | 55130 |
| rs561717884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27884523 | CCAAAGTGGAAGTTG[C/T]TTGCCATGTTTTGGC | 55130 |
| rs561749828 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27838014 | AGATCCTAAGAATCT[A/C]AGATTTTTGTATTTT | 55130 |
| rs561773128 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27931455 | TTCTCATCATCTACT[G/T]TACTATTTTAAAATT | 55130 |
| rs561784604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27845238 | TTGGCAGAAACTATA[C/T]AAGCCAGAAGAGAGT | 55130 |
| rs561784873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27837401 | TCTGGCAAGTCATTT[C/T]CTAGGCAAGTGATCA | 55130 |
| rs561807156 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27963749 | TCACACTCCAATAGA[A/G]GTTATCATATAATAT | 55130 |
| rs561834977 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27924516 | CAGAAATTTATGTGG[C/T]AGAAAATAAAAGAAC | 55130 |
| rs561843787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27863423 | AGCCTCAGCTGAGAA[C/T]GTGTGCATTGGACGA | 55130 |
| rs561881357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27870236 | CAATCTTTTCTCTCC[C/T]AATCTCAATCTTTTC | 55130 |
| rs561892460 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27856567 | TTAATGGCTTAATAC[A/C/G]CCCTGCTGAATTTCT | 55130 |
| rs561898920 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27849012 | TTCCTCAAGGATCTA[C/G]AACTAGAAATACCAT | 55130 |
| rs561924185 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27970059 | TGCAGTGAGCCAAGT[G/T]TGTGCCACTGCAGCC | 55130 |
| rs561925132 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27978804 | CTCAAAAAAAGAAAA[A/G]AAAAGGAAAACTGAA | 55130 |
| rs561940414 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27992906 | CATCTGCTTTAAATG[C/T]ATTTTTATAAAAAAA | 55130 |
| rs561959869 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27963157 | GACTTACAGGCATGC[A/G]CCACCACATCTGGCT | 55130 |
| rs561964012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27937646 | GCAGAGACTTGGCAA[C/T]TACTCCAAGCACACA | 55130 |
| rs562009358 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27850159 | TGTTTAAAGTGAAAA[C/T]ATTTGCTGGGCGTGG | 55130 |
| rs562022996 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27844155 | AGCTATGATCGTGCC[A/T]CTGTACTCCAACTTG | 55130 |
| rs562031409 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27901898 | CAGTATTAGATCAAC[A/G]AGACAGAAAATTAAC | 55130 |
| rs562044945 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27857158 | AGACCAACTCAACTT[C/T]TTCCTCCTCCTCTTC | 55130 |
| rs562068690 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ARMC4 | GRCh38.p7 | 10:27998973 | GCCTCACCCGGCCGC[A/G]ACCGCAGCCCAGTCC | 55130 |
| rs562071299 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27909336 | AAAAGGAACATTCAA[A/T]CCTGGACAAAATTTC | 55130 |
| rs562084100 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27969463 | AGGAATCTCATGCTT[G/T]AAAGAGTAAGAATAT | 55130 |
| rs562097165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27816835 | CTCACTGCAACCTCC[A/G]TCCCCTGGGGTTCAA | 55130 |
| rs562101474 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27823790 | GGTTCATGGTGTCCC[A/G]TTAGATAGTCAAAAA | 55130 |
| rs562115444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27904212 | GGCTCCTGCAATGTG[A/G]TGCACATTCCTAAAG | 55130 |
| rs562134172 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27823223 | TTAAATATAAAGAAT[A/T]TTGGCACACATAGGG | 55130 |
| rs562139134 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27929916 | TCTTTTGGGGTCTTT[G/T]TGAGATAAAGACTCA | 55130 |
| rs562149542 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27950767 | CATATGCATTCTTTT[C/T]AATTTGCCATGGAAC | 55130 |
| rs562168970 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27874744 | TAGTCTGATGGGCTT[C/T]CCTTTGTGTGTAACC | 55130 |
| rs562214069 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27923099 | ACAAAGAACAAAGAC[A/T]GCAAATCTTATAGCA | 55130 |
| rs562219235 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27830768 | TGGAGATTCAATAAA[C/G]TCATTCCTTCAATAC | 55130 |
| rs562220493 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27929904 | ATATTACTAAGATCT[A/T]TTGGGGTCTTTTTGA | 55130 |
| rs562234119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27927566 | ATTTATAAAAACACA[C/T]GTGGGACGCCTATGT | 55130 |
| rs562285257 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27877856 | AAAGGACTTCCACAT[G/T]CATTATCTCATATGA | 55130 |
| rs562316711 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872597 | TCAAAGGCCTTTCCT[C/G]CATCCATTGAGATAA | 55130 |
| rs562322455 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27886741 | TTGTGGCATTCATAA[C/T]GTAGTGTGTGGGTGG | 55130 |
| rs562324755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27965867 | TTATTCCTCATCGCT[C/T]TAGAAGTTTCTAACT | 55130 |
| rs562326975 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ARMC4 | GRCh38.p7 | 10:27823997 | TACAAAAAATTAGCC[A/G]GGCGAGGTGGCGGGC | 55130 |
| rs562328740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27979435 | ACCTAAGAATACACA[C/T]ACACACCCATACACA | 55130 |
| rs562361447 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ARMC4 | GRCh38.p7 | 10:27885308 | CGAGATCAAGAGATC[A/G]AAACCATCCTGGCCA | 55130 |
| rs562371438 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27917831 | GGAGAGAGAGAAAAA[C/T]GAGAACTACTATCAT | 55130 |
| rs562378590 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27965533 | AAGATACGGAGGAGA[C/G]TCCAGGAGGAGACAG | 55130 |
| rs562382014 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27922079 | GGCTGAGGTGGAAGG[A/T]TATCTTGAGCCCAGA | 55130 |
| rs562419663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27930635 | CTGTCTCAAAAAAAA[A/G]AAAAAGAAAAAGAAA | 55130 |
| rs562427737 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27850966 | ACCACAGCCACTAGA[C/G]TCTTCAGGGCAGATA | 55130 |
| rs562433284 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27892288 | AATGTTCAAATAAAA[C/T]TTCTTTAAAAATATG | 55130 |
| rs562435129 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27859722 | CATGTGAGCTGTTCA[G/T]GTACTCTAAGTATTT | 55130 |
| rs562446232 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27977283 | AAAAATACAAGACTC[A/G]GCCGGGCACGGTGGC | 55130 |
| rs562463677 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27958572 | TCACTCTACTTCCCC[C/G]CTTTTATTGGTTGCT | 55130 |
| rs562466631 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27911389 | TTTGGGGGTTATAAA[C/T]AAAGTTTAGAGACTG | 55130 |
| rs562484449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27972997 | CCAAAATAGATCATA[C/T]ACTGGGCCATAAAAT | 55130 |
| rs562485706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27959437 | AGGTAATCACAGGAG[A/G]CCCTGTGGTTCAGTA | 55130 |
| rs562490937 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27978858 | CTAAAGGTCATATAA[G/T]AAAATCCCACAGCTA | 55130 |
| rs562493234 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27818703 | AACTCCACCTAATAT[C/G]TACCTCTCATGGCCA | 55130 |
| rs562505081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27857909 | ATAACAAGCATTTGA[C/T]GAGAAGTCGGCAGCA | 55130 |
| rs562507420 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872106 | CCTAGGTATTTTATT[A/C]TCTTTGAAGCAATTG | 55130 |
| rs562535593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27951522 | GATAGGCCAATAATC[C/T]GTGTTGATACAATTG | 55130 |
| rs562552332 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | ARMC4 | GRCh38.p7 | 10:27986843 | ATATTTGCCACAAAG[A/T]TGAATGACTGTAACT | 55130 |
| rs562552736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27925361 | TAATAAAAACACTTT[C/T]TAAAAAATGTTTTTG | 55130 |
| rs562561984 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27965165 | CAAAATTGTCAGTGA[C/T]AATGGATCCATAGAA | 55130 |
| rs562575096 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27861724 | TGTATACGTAATTGC[C/T]CTGTAATGGGCATAC | 55130 |
| rs562597140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27957877 | GAGACATCACTCTAC[C/T]TGGAAAATGGTAAAT | 55130 |
| rs562611636 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27945262 | TGAGGAATGCAAGAT[A/G]TACACAGAGCTAAGA | 55130 |
| rs562626986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27918413 | ATAGAACAAAAGAAA[A/G]ATCACCTTATTTATT | 55130 |
| rs562639632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27857322 | CTAATACATAATACA[C/T]ATAACATACGAAATA | 55130 |
| rs562648382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27939375 | ATCTGCCATTACCAC[A/G]GGACAATGGTTCTTA | 55130 |
| rs562675880 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27941960 | ACTGGCTTGAGACAG[A/G]TGGACACTCCTGGTC | 55130 |
| rs562678387 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27864187 | AAGATTGTGGATTTG[A/G]GAAGCTTGCTTGGAG | 55130 |
| rs562684824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27900252 | AGGAAAACTAACAAA[C/T]AGAAAGGAATAGCAT | 55130 |
| rs562692932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27957399 | GCGAGCCTGTGCACA[C/T]TAGCAAGATGCCCTG | 55130 |
| rs562712129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27838098 | AGGAGGGAATATTAA[C/T]GCGAGCATATTTTTG | 55130 |
| rs562724887 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27972320 | ATAAATAAAATGGAA[C/T]CATTTTAAAAAGCTC | 55130 |
| rs562750093 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27994535 | AGGAATTTGAGACCA[A/C]CCTGGGCAACATAGT | 55130 |
| rs562757246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27893805 | TGCAAGCTGGATGCC[C/T]CAGCATATTCAAAAA | 55130 |
| rs562762053 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27957473 | GTAGATAGTAAGACA[C/G]ACAACCTGAACCATC | 55130 |
| rs562769548 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27831312 | TTTTTCATCATCACC[G/T]AAAACGACATTCCCC | 55130 |
| rs562784211 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27824758 | CTTGGGTTCTCTCCC[A/G]TTGGCATGAGATTGA | 55130 |
| rs562795863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27824581 | TATATTCTGTTATAG[C/T]AGCAGAAAATGGACT | 55130 |
| rs562808714 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27830957 | TTTGGCAGGTGGACA[C/G]GTCCTTTTTCCTTTG | 55130 |
| rs562808737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27837222 | TGACCACATGGTCCC[A/G]TACTGGTCACTCAGA | 55130 |
| rs562811573 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27914969 | AAATGAAACAACATA[A/T]GCATGATTGGAATAC | 55130 |
| rs562836887 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27917148 | AGCTGAGTCATAAAG[C/G]CTAATATGAAAGAAC | 55130 |
| rs562840020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27904607 | TTCTATCCTATTCCA[C/T]TGGTCTGTCTGCCTG | 55130 |
| rs562846044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27836710 | CATAATTTCTTTAGG[A/G]TTTCAAGGAATACGA | 55130 |
| rs562862033 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27949386 | GGGGCATGGAGCTGT[A/G]GAAGCACATCACAGG | 55130 |
| rs562873798 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27871172 | TGAGAAGTGTCTGTT[A/C]ATATCCTTTGTTCAC | 55130 |
| rs562874849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27993572 | GGAGAATTGCTTGAA[C/T]CAGAGAGGTGGAACT | 55130 |
| rs562942496 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27854639 | TGCATGCCTGTAACC[A/C]CAGCTACTCGGGAGG | 55130 |
| rs562955042 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27817482 | CAATAGGTAATTTTT[A/T]AACCCTCATTCCCCC | 55130 |
| rs562965347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27910013 | AAATTTTACTTCACA[A/G]TGACTCAAGTATCTG | 55130 |
| rs563004617 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27910660 | TACTTGGGAGGCTGA[G/T]GTAGGAGGATGACTT | 55130 |
| rs563043024 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27986024 | GGAGAGGAAGGCCTA[C/T]GAGACTAATTCAGAA | 55130 |
| rs563046726 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27851488 | TCAACATGTCAAGTA[A/G]AGACACGAAAGATGT | 55130 |
| rs563054764 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27936997 | AGAGAGATCATTTTC[A/G]AAAGATGCCTCCAAG | 55130 |
| rs563056013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27916194 | ATAGTAGAGCAGCAT[A/G]ACAGGAGATCAAAAG | 55130 |
| rs563076199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27963791 | ATTTCATTACCCTTT[C/T]TTGAAGTGAGTTTTT | 55130 |
| rs563089982 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27823878 | GGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 55130 |
| rs563094634 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27920279 | ACTTTCCCTTATGTA[C/T]AGTTTACAAATTAAA | 55130 |
| rs563118861 | snp | A/G | | | utr-variant-3-prime, intron-variant | ARMC4 | GRCh38.p7 | 10:27812387 | GCATTTTCAATTTGT[A/G]TGTTTTCATTTAGAT | 55130 |
| rs563139696 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27816424 | CCTTTTCTCCAGCAT[C/T]GTTCAATATCCTAGG | 55130 |
| rs563141328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27970132 | TAAATAAATAAATAA[A/G]TAAATAAATAAATAA | 55130 |
| rs563181084 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27868272 | GAAGACAGTGTGGTG[A/G]TTCCTCAAGGATCTA | 55130 |
| rs563200413 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27844518 | GCAATACCTTCCAAT[C/G]GTGGTTCAGAGAGGA | 55130 |
| rs563220649 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27923791 | CATCTCTACAAAAAA[A/T]TTTTGAAATTAGCTG | 55130 |
| rs563238405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27970775 | TTGAGACCAGTCTGG[C/T]CAACATGGTATAACC | 55130 |
| rs563261974 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27848879 | ACCAGTTAGAATGGC[A/G]ATCATTAAAAAGTCA | 55130 |
| rs563263028 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27841556 | GCCCGCCACCATGCC[C/T]GGCTAATTTTTGTAT | 55130 |
| rs563263156 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27871416 | TTTGGTGTTTTAGAC[A/T]TGAAGTCCTTGCCCA | 55130 |
| rs563271261 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27885325 | AACCATCCTGGCCAA[C/T]GTGGTGAAACCCTGT | 55130 |
| rs563274876 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27977798 | CATGAAAAGATGCAT[A/T]CAAGAACTGCAAATT | 55130 |
| rs563276017 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27908748 | TTGATTATCTTAGAT[G/T]AGTTTACCAGGGGGG | 55130 |
| rs563307715 | in-del | -/TCTTAATAGGAAAAAAGAACTTT | 0.0107246 | 0.0724382 | intron-variant | ARMC4 | GRCh38.p7 | 10:27892215 | TGTCCTTTTTAGCAA[-/TCTTAATAGGAAAAAAGAACTTT]TCTTAGACATAACAC | 55130 |
| rs563313232 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27895630 | CTCAAAATTCAGTTA[C/T]TTGGCCCTACTAGTC | 55130 |
| rs563315496 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27843362 | ACAAAGCTTGAATGC[A/C]ATTGTAGCGGATGGT | 55130 |
| rs563330191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27949475 | GGACAGAAAATAGGC[A/G]ATTTCCCAGGCAGAG | 55130 |
| rs563352381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27840601 | GAAAATGGGGGTGGA[A/G]AAAATATGTGGCCTC | 55130 |
| rs563399135 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984559 | TTAGAAAATGAACAT[G/T]CTTTGGACTATACAA | 55130 |
| rs563438865 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27813279 | AAAACAGACCTAGCC[A/G]ACTTTTCCACGAAGC | 55130 |
| rs563441157 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27898843 | TGAGATCTTTTTAAT[A/T]TTTTGGCTGTGATAA | 55130 |
| rs563446613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27991005 | CATGTGATTCTGAGC[A/G]CTTATCCAATTTATA | 55130 |
| rs563447562 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27998245 | TTACTCAGTAAGACC[G/T]ACAGAAAATCGAACT | 55130 |
| rs563502808 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983163 | TTTGTTGATTTTTCA[C/T]GGTCCCAGAAACAGG | 55130 |
| rs563503366 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27868934 | TCTTACGATGAAAGC[A/G/T]CATTAGAAAGACATG | 55130 |
| rs563503978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27903564 | CCCATCGTCTCAGCC[A/G]AAAATCTCCTTAAGC | 55130 |
| rs563523650 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27890203 | GGTCACAGTGCAATG[C/G]GAGTGCTTAAGCAAG | 55130 |
| rs563525421 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27880816 | ATAAATTATCCAGTC[G/T]GTAGTATTTTGTTAT | 55130 |
| rs563615252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27928928 | GTATATGGTGACCAA[A/G]ACACTGAGTCATTTA | 55130 |
| rs563631070 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27869530 | TCACTTTTTTTTCTT[C/T]TTTCTTTTTCTTTTT | 55130 |
| rs563635521 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27978864 | GTCATATAAGAAAAT[A/C]CCACAGCTAACATCA | 55130 |
| rs563642568 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27923952 | CTGTCTAATGAAAGA[A/G]AGAAAGAAAGAAAGA | 55130 |
| rs563645696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27949952 | CACGCTTGCAGGGTC[A/G]TCATTTGAAGTTATT | 55130 |
| rs563646045 | in-del | -/AAAG | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27882177 | GTCATAAAAAAAAAG[-/AAAG]AAAGAAAGAAAGAAA | 55130 |
| rs563663185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27946824 | TTAAAATAAGAAACC[A/G]AAATAGGATTGATTA | 55130 |
| rs563666566 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27982422 | TTTGATAGAAATAAA[A/G]ACTCCCTGCCCCCCT | 55130 |
| rs563666725 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27990043 | GTGACCTGATGGAGA[A/C]ACTTTTAAACCAGAA | 55130 |
| rs563669445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27875418 | TGCGTTCCTTTGGAG[A/G]GGGAGAGGCACTCTG | 55130 |
| rs563688699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27955276 | AAGAGCACAGTCTAA[C/T]ATGGCCTTCCAAACA | 55130 |
| rs563691451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27923935 | GGTGATAGAGAGAGA[C/T]CCTGTCTAATGAAAG | 55130 |
| rs563707304 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27947930 | GCAATTTTCGAGCTT[A/G]TACACTCAGCACAAT | 55130 |
| rs563710832 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27837032 | ACTGCCCACCGTGAG[A/G]ATTTCTGGGACTCGT | 55130 |
| rs563731204 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27975411 | ATCAAAACAAAAAAA[A/C]CACAAATGACCAATA | 55130 |
| rs563741560 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27835349 | GTGAGATGTGAGAAA[C/G]AGCAACTTCGAAAGT | 55130 |
| rs563829002 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27929730 | AATATTTTTTCTCTC[C/T]CAGGATGTTTTAATC | 55130 |
| rs563843530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27976442 | GCATACAAAAATCAA[A/G]TGTATATTTATACAA | 55130 |
| rs563848667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27854061 | AAACAACCTAATTAA[A/G]AAGTGGTCAAAAATG | 55130 |
| rs563869778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27974760 | ATTTTAAAATAGTTT[C/T]TTCTAGTTCTGTGAA | 55130 |
| rs563909419 | in-del | -/TTTG | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27952886 | ATAAACCAAGTTTGT[-/TTTG]TTTATTACTCTTCAT | 55130 |
| rs563912070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27898856 | ATTTTTTGGCTGTGA[C/T]AACAAATGATTCCAT | 55130 |
| rs563921348 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27935526 | TTCCACTCTACTAGG[G/T]TTTTTTCCCCCTATC | 55130 |
| rs563949372 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27834395 | CAGGCATCCCTTACA[C/T]AGGGCAAGAAACACA | 55130 |
| rs563950552 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27899235 | CTCCCCTAGCCAAGG[C/G]AAGGGGGAGTGTGGG | 55130 |
| rs563952590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27848256 | AGAACAGAGCCCTCA[A/G]AAATAATACTACACA | 55130 |
| rs563982577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27942067 | CGTGGGAAAAATTCT[A/G]AGACCGTGGGATTGA | 55130 |
| rs564051010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27902501 | TCAAAAAATCAATGA[A/G]TCCAGGAGCTGGTTT | 55130 |
| rs564058146 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27970931 | GAGCTGAGATGGCAC[C/G]ACTGCACTCCTGCCT | 55130 |
| rs564073801 | snp | C/G | 0.00119737 | 0.0244387 | utr-variant-5-prime, intron-variant | ARMC4 | GRCh38.p7 | 10:27998821 | CAGCACCCTGCCCCC[C/G]GCAGTCGGCGCCCGC | 55130 |
| rs564123904 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27884348 | CTTTGAAAATCAGCT[A/C]AGATATCTAAAGAAA | 55130 |
| rs564147214 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27993192 | AACGTTGGGATTACA[A/G]GTGTGAGCCACCATG | 55130 |
| rs564169536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27937086 | TGGCTTTGGGAATGG[A/G]TAGCAGTTTCTAAGT | 55130 |
| rs564189074 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27937530 | TTTATTCAAATATGC[G/T]TATCCATGTTTGTGT | 55130 |
| rs564212605 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27977903 | GAGTATGTGGAAGAA[C/G]TGGGACTCTCATACA | 55130 |
| rs564224112 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27931391 | AAGTCAAGCCACTCA[C/T]AAAACTCCACAAACT | 55130 |
| rs564224981 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27849460 | AATGTAAATGACGAG[A/T]TAATGGGTGCAGCAC | 55130 |
| rs564283865 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27908900 | AAAACTGTCTTAAAA[A/C]GGACTTCTAATAAGA | 55130 |
| rs564312226 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27985494 | TTCTTTCTTTTTTAA[G/T]TGGCCGTGGGGCATT | 55130 |
| rs564314667 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27815911 | AAGTCTCACAGCCAC[C/T]TCAAGCTTAATAGAT | 55130 |
| rs564315328 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944144 | ATGGAATTTCCAGCG[A/T]GGCCAGAAAGGACAG | 55130 |
| rs564357208 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27816799 | TTTTGCCCAGGCTGG[A/T]GTGAAGTGGTGTCAT | 55130 |
| rs564376353 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27956488 | ATCCAACTGTGCTTG[C/T]CAATATAACCCTTGT | 55130 |
| rs564380028 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27950549 | TATCAGGAATGGGTA[A/C]GGACAATACAAGGAT | 55130 |
| rs564425688 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27848770 | ACTTCTCAAAAGAAG[A/T]CATTTATGAAGCCAA | 55130 |
| rs564457265 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27876648 | TGAGGTCTGAGATAA[C/T]GTCTCTGAGGAATCC | 55130 |
| rs564463373 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27823080 | ACTGGCTGGGTCAGG[C/G]AATTGTGGGACATTG | 55130 |
| rs564469081 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27956086 | TCCACGCCAGTGTTT[C/G]ATGAATTTGATGATA | 55130 |
| rs564473415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27870107 | GATCTCCAAAAAGTC[C/T]AGAAGGACATTAACA | 55130 |
| rs564497215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27830688 | ACTCGTCTGAATATT[C/T]TCCCTGGAGCACTGG | 55130 |
| rs564499108 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27822461 | CCCTTCTGACATTCT[A/C]CTGTTTACAAGGCAT | 55130 |
| rs564500545 | in-del | -/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27824062 | GGAGAATGGCGTGAA[-/C]CCCAGGGGGCGGAGC | 55130 |
| rs564537259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27830111 | TGCTCCCCATAGAGA[C/T]CCTTGAAGTACCTTC | 55130 |
| rs564538128 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27956544 | ATACGGGCATCTTAT[C/T]CTGTAGTGACAGCTC | 55130 |
| rs564544419 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27969381 | CAGGGCCTGCACCTG[C/G]TTTTCCAGGTATTCG | 55130 |
| rs564562978 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27835434 | CAACCGCTGCAGCAA[C/T]ATTCAGATACACCCA | 55130 |
| rs564629202 | in-del | -/GGAAAAA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27845144 | GAAATGAAGGAAAAA[-/GGAAAAA]ATGTTAAGTGCAGCC | 55130 |
| rs564645632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27948221 | TTTTTTCTGAAAATC[C/T]GGAAACATATTCATA | 55130 |
| rs564708878 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27918070 | AAAAAAACTCCAACT[C/T]AGATAATTCTGCTAA | 55130 |
| rs564712382 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27864798 | TTTCTCAAATAATAA[A/T]AATTCACATCTTTTG | 55130 |
| rs564733512 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27989645 | ATTTTTCATTGCTCC[C/T]ACCAGTTGAAGCCTG | 55130 |
| rs564738750 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27928153 | ATAATAATGAACATA[C/T]TGACTTTGTCTCTCC | 55130 |
| rs564763713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27828547 | ATTTTCTGGCTTTTA[C/T]TTCATTTTCTTAAAT | 55130 |
| rs564769674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27942771 | CCTCCCTACATCCAC[C/T]ACCTGGAGTCTCTAA | 55130 |
| rs564769982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944495 | GTTTTTAAAAATTCC[A/G]AGTATACCTAAAATC | 55130 |
| rs564778469 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27894608 | TTGAGACAGGGTCTT[G/T]CTTTGTTGCCCAGGC | 55130 |
| rs564778958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27929062 | AAATGGGATTGTACA[A/G]GGTGTTAAACAAGAA | 55130 |
| rs564794503 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27954669 | TATCATTGTCTTTAC[A/G]CTGCTTTTTCTCCAC | 55130 |
| rs564802756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27834462 | AACCTAATCATCACA[C/T]GGCCACACCAAGACT | 55130 |
| rs564819034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27928160 | TGAACATATTGACTT[C/T]GTCTCTCCTCTCATG | 55130 |
| rs564848396 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983785 | CACACCCTTGAGACA[A/T]CTACAGCTAACAATC | 55130 |
| rs564857505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27860974 | GGGCTAGCTGGCTGA[C/T]TACCTAGGTGATGTT | 55130 |
| rs564892057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27913598 | TGCATCTGACAAAAG[C/T]CTAATATCCACAATC | 55130 |
| rs564896091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27868252 | AAATTAGTTTAACCA[C/T]TGTGGAAGACAGTGT | 55130 |
| rs564907266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27990811 | CCATTGCTCTGGTGA[C/T]CTGACTTCCTGTCCC | 55130 |
| rs564914893 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27814853 | AATAACTGAGTCCTG[A/C]GGGAGGCATATGTCA | 55130 |
| rs564920660 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARMC4 | GRCh38.p7 | 10:27820732 | TATCCCATATGCTGG[C/T]TGGTTAAATTTTAGC | 55130 |
| rs564943887 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27862012 | TAAACAATGAAATGA[C/T]TGCCAAAGTCTTCTA | 55130 |
| rs564966166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27915488 | AGGCCTCTACCCTCA[C/T]GTCCTAATCACTTCC | 55130 |
| rs564984833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27927290 | ATCCTGATATGTGAC[C/T]CAAGTTTTTACCATA | 55130 |
| rs564991817 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27914135 | CATACAAACCATGGA[A/G]TACTACACAGCCATA | 55130 |
| rs564993999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27824899 | AAGCTGGATTTTACT[A/G]AGATTTCCCCAGAAT | 55130 |
| rs565053356 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27920601 | TCTCAGTTAAATCTA[C/T]GTGCTTTAAAAGTAT | 55130 |
| rs565078548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27874079 | GGATAGTTAGTTCTC[C/T]TTGTTGAATTGATAC | 55130 |
| rs565151772 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27888256 | GTTTTCTATAGAAGT[C/T]ACACTAATTTACATT | 55130 |
| rs565220026 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27873466 | GTGTCAATTTTAGAT[A/C]TTTCCTGCTTTCTCT | 55130 |
| rs565240469 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27965639 | AGTAGTGTATTCATT[C/G]TGGCTTCCCATTAAT | 55130 |
| rs565258129 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27828865 | ATTCTCTAAATTATA[C/T]CCATATTAAAAATGA | 55130 |
| rs565260501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27879710 | GTTGGATCTGTTACA[C/T]ACATTTTTCTGAAGC | 55130 |
| rs565263217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27889233 | TCAAGTTGGACCCAA[C/T]CTTCTGACCAGAAAC | 55130 |
| rs565264808 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27973980 | AACAGCCATTCTGAC[C/T]GGTGTAAGATGATAT | 55130 |
| rs565270361 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27906131 | TCTGACAAAGGGCTG[A/C/G]TATCCAGAATCTACA | 55130 |
| rs565274951 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27977258 | CTTTGAAAGACATTG[C/T]TTAGAGAATAAAAAT | 55130 |
| rs565299040 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27968198 | ATGGAAATTTTGGAA[C/G]TAAAAATTATAAGTG | 55130 |
| rs565301293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27966536 | TTTTCCTATTTGATA[C/T]GATTTCTTCCAATCC | 55130 |
| rs565302094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27974620 | AGTACCATGTTGTTT[C/T]GGTTACTGTAGCCCT | 55130 |
| rs565319000 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27918029 | TTGTAATTTTAAAAA[C/T]CAATTAAAAAGGAAT | 55130 |
| rs565337641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27969104 | TGTAGATATATACTC[C/T]GTTATTTCCATGTGC | 55130 |
| rs565347404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27988741 | TTACTTATTACTGAC[A/G]ATCTCACTAGAATAA | 55130 |
| rs565367943 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27946907 | ACTCCATTTAAGAAA[A/G/T]TTTCTTCCATGCCTC | 55130 |
| rs565394509 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27819206 | GGAGGAGCACAGGTC[A/G]GGGGAATTTACACTG | 55130 |
| rs565403903 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27853162 | TCACGAGGTCAGGAG[A/T]TTGAGACCATCCTGA | 55130 |
| rs565432076 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27841958 | GATAGGGTCTCCCTA[A/T]GTTGCCCAGGCTAGT | 55130 |
| rs565441032 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27930746 | AGGAAGTTACTTGAA[G/T]TTATCTGTTTGCTTT | 55130 |
| rs565441900 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ARMC4 | GRCh38.p7 | 10:27904774 | TCAACTTACCAACTC[C/T]ATGAAACAAAGCTTG | 55130 |
| rs565469303 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27847969 | CTTGGATAGGAAGAA[C/T]CAATATCGTGAAAAT | 55130 |
| rs565470523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27946307 | ATTCCATACCAGCTG[C/T]CAAACTCCCTCCTCC | 55130 |
| rs565495820 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27847494 | CAAAAATGAAGCATT[C/G]CCTTTGAAAACTGGC | 55130 |
| rs565497239 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27834930 | GGATGGAAACCTGAG[C/T]TATCCTATATTATGC | 55130 |
| rs565527542 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27874451 | TTTCTTCCTAGCATC[A/G]ATGGTCTTTACATTT | 55130 |
| rs565534072 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27953063 | ATGAGTTTGGGTATA[C/T]GCATATAAATCCAAC | 55130 |
| rs565537551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27941254 | TTTAGGAGCTCGAGG[C/T]GGGAGGATCACTTGA | 55130 |
| rs565558792 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27906918 | ACCTAATGTAGATGA[C/T]GGGTTGATGGGTGGA | 55130 |
| rs565563144 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27881119 | ACTCTTCAGGATTGT[G/T]AAAAGGATACATATT | 55130 |
| rs565564110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27941761 | CCTTGCAGGCTCACT[A/G]TCTCTATCTGGGGCT | 55130 |
| rs565576552 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27859387 | TTAATTTCAGAAAAA[A/T]TAACATCATATTCTT | 55130 |
| rs565606420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27995224 | AACAGCGTCCACCTT[C/T]TCCTTGGAACATTTT | 55130 |
| rs565638003 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27975881 | ACTAATAACTTTATG[A/C]ATATAGGTGCAAAAC | 55130 |
| rs565654651 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27881703 | TAGATAATAATTCTA[A/T]GTTTATATAACTAAA | 55130 |
| rs565667077 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27877847 | GCAATTTATAAAGGA[C/T]TTCCACATGCATTAT | 55130 |
| rs565667905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27975023 | TGGGATTGCATTCCT[A/G]ATTTGGCTCTTGGCT | 55130 |
| rs565689043 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27954765 | CCCCTTTGGGAAAGA[C/T]GGAGAGGAGCCTCTC | 55130 |
| rs565692714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27913198 | TAAATTACGTGTCGC[A/G]GGGGTTTGGTGTACA | 55130 |
| rs565711782 | in-del | -/T | 0.00716266 | 0.059414 | intron-variant | ARMC4 | GRCh38.p7 | 10:27918333 | ATATGATCAGAGTGA[-/T]TTTATCCAAGGAATA | 55130 |
| rs565742180 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27889672 | CAGTTTCACACATGG[A/G]CACTCCCATGGACTT | 55130 |
| rs565767900 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27935693 | GAGTAGTAGCTTGTG[C/T]TACTTGGATAAAAAA | 55130 |
| rs565780886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27827904 | GCTTCTCTTCTTTTT[C/T]CTGTGACTATATATT | 55130 |
| rs565798518 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983413 | CTGGGTCCCAGCTTC[A/G]TAGGGCACTGTCTCC | 55130 |
| rs565812298 | in-del | -/AATA | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27840085 | AAATAAAACAATAAT[-/AATA]AATAAAACCAGCCAA | 55130 |
| rs565824251 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27881013 | AGCACATCCTAGCAT[C/T]CATCACTATCAGCAA | 55130 |
| rs565828608 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27907021 | GTATAATTTAAAAAA[A/G]AATTCAACAGGCAGA | 55130 |
| rs565830972 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27853759 | TAAAAAAGTTTACTC[A/G]AATGGGTCATAGACT | 55130 |
| rs565831525 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27902151 | CTCAGGATTAAGAAA[A/C]TCTCTCAAAACCACA | 55130 |
| rs565834289 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27989724 | CATGGTGGCACGTGC[G/T]TTGGTCCCAGCTACT | 55130 |
| rs565835440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27854329 | AAAGGTACACATACC[A/G]TATGATCCAGCCATT | 55130 |
| rs565837669 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27839315 | GAAGGCAATGGCTTC[C/T]GGCTTCACTCAACTC | 55130 |
| rs565841491 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27914192 | ATTAAGTGAGAGCCA[A/G]TTATATCCCATGCAT | 55130 |
| rs565848508 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27949528 | TCCACCAGTCGGAGC[A/T]AACAGTATATGCAAA | 55130 |
| rs565863955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27901729 | AAGGGCATTGCATAA[C/T]GGTAAAGGGATCAAT | 55130 |
| rs565871641 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27977691 | AAGATCTGTTGCAAC[C/T]CAATAAAAAACTGAA | 55130 |
| rs565871655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27861082 | CTGCAAGCTCGGCCT[C/T]CTGGATTCAAGTGAT | 55130 |
| rs565883594 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27896815 | ACACACATGCCTCTT[C/T]CATGTTTATCACTTC | 55130 |
| rs565900531 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27866323 | CAGGATTTGATTCCA[A/G]ATCTGTCTGACCCCA | 55130 |
| rs565906992 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27836687 | AAATCATTAGTTTTA[C/T]GGTAGGACATAATTT | 55130 |
| rs565912929 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27960433 | CTCACTGCAACCTCC[A/G]CCTCCTGGGTTCAAG | 55130 |
| rs565990790 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27907526 | TCCGAAATTATTTTG[C/G]CATAAACATTGTGCA | 55130 |
| rs565994342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27989213 | CATTAGGTTTGGGGC[A/G]ATGTGTTACAGCAGC | 55130 |
| rs566063198 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27833454 | AATAAAATGCATCGT[A/G]GGAACTCAGCCCCTC | 55130 |
| rs566086433 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27995261 | TCAAGACTTTAAACT[A/C]GTACTCCCCATCCCA | 55130 |
| rs566096410 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27900576 | TTGAAAAACAGGTTA[C/G]AGAAATTGCTAACTA | 55130 |
| rs566127165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27879004 | AGAAATGATACAATC[A/G]TTATAGTCTAGACTT | 55130 |
| rs566128802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27895069 | AACTGTTAGCTCTTA[A/G]TATCAGTTATCCCCA | 55130 |
| rs566163184 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27994292 | CATCACCCCTCCCCG[A/C]CGCCTCCTGCTTCTA | 55130 |
| rs566180454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27926496 | TATGAAGAAACCTTT[A/G]AAACACTCTTCAAAG | 55130 |
| rs566182984 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27912766 | CAACATTAAAGGATG[C/T]GACTGTCATCTACAA | 55130 |
| rs566205147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27959746 | TAACATTTCATTTAC[A/G]TGTCTTTAAATAATA | 55130 |
| rs566224949 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:28000457 | ACCTGTGGCGGTAAT[A/G]CAGGTCACAACCTGG | 55130 |
| rs566226243 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872841 | CTGTGTCTCTGCCAG[C/G]CTTTGGTATCAGGAT | 55130 |
| rs566230965 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27826268 | ATCATTCTTCTCCTA[C/T]AGTGATATTACAAAT | 55130 |
| rs566244073 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27973492 | CTCCCTCCTCCCACC[C/T]TCCAATCTCAAGTAG | 55130 |
| rs566244492 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27933520 | AGGCGGAGACTAGAG[G/T]TGATGCCAAATAGGA | 55130 |
| rs566257369 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27931765 | GTGGCAACTAGATAA[A/C]CTGGCAATGACTTAC | 55130 |
| rs566271983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27980576 | TATGAAAATATGGTC[A/G]ACATTACTAATCATT | 55130 |
| rs566278846 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27966210 | CTGGAAGAGGGAAAG[A/C]CTGAATTCAAGCATC | 55130 |
| rs566280848 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27974065 | TCACATGCTTGTTGG[C/T]CACATGTATGTCTTC | 55130 |
| rs566313044 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27865626 | GTCCCAGGAGGGTGA[A/G]GACTCTTGCTGTCTC | 55130 |
| rs566328598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27932950 | CTCAATAAATATGTG[C/T]TTAATGTAAAGGAAT | 55130 |
| rs566342248 | snp | A/T | 0.0267878 | 0.112589 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940277 | TGTGATATATATATA[A/T]ATGCCAGTATATATG | 55130 |
| rs566345197 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27871788 | TTGAAGTCAGGTAGC[A/G]TGATGCCTGCAGCTG | 55130 |
| rs566355284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27979817 | TAAATTCAATGAAAT[C/T]TCTATCAAAACCCAA | 55130 |
| rs566368819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27846985 | TCACAGCCAAATTCT[A/G]CCAGAAGTACAAGGA | 55130 |
| rs566371661 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999986 | GGAGTGCAGTGGCAC[A/G]ATCTCGGCTCACCGC | 55130 |
| rs566372280 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27850027 | AAATCTACTAATCAA[A/G]TGGACACAGCACTAA | 55130 |
| rs566418670 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27987750 | AGCAAGCCTAGTGAC[A/C]AATAGGATATAACCA | 55130 |
| rs566481834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27845447 | GGAAAGGAACAGCTG[A/G]TACCAGCCACTGCAA | 55130 |
| rs566487037 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27866598 | GCAGGCTTTACAAGA[A/C]ACATGGTGCCAGCAT | 55130 |
| rs566527694 | in-del | -/AA | 0.494609 | 0.0516363 | intron-variant | ARMC4 | GRCh38.p7 | 10:27943795 | GTGAGGCTCTGTCTC[-/AA]AAAAAAAAAAAAAAA | 55130 |
| rs566536269 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997627 | TCTAGTGAACCGTAG[A/C]AATGCACAAGTTTTA | 55130 |
| rs566537061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27971824 | TTCTTTACTAAGAAT[A/G]AAACAAAAATCTTTC | 55130 |
| rs566575569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27928620 | ATTTGCCATTTAAGG[C/T]CCCTTGTTTCAATTT | 55130 |
| rs566618085 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27845016 | TATTTTAGAAGTCAG[C/G]TGAATCAGCAAGGCA | 55130 |
| rs566635803 | in-del | -/AGGGGGG | 0.492037 | 0.0625946 | intron-variant | ARMC4 | GRCh38.p7 | 10:27908756 | TTAGATGAGTTTACC[-/AGGGGGG]AGGGGGGAAAAATGT | 55130 |
| rs566637672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27865225 | GGCTCTCTATGTGAG[C/T]TAATAATAAGAACCC | 55130 |
| rs566643033 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27878235 | GCTTAAATAAGTAGG[A/G]AAAGGTATGAAGTTC | 55130 |
| rs566645792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27958260 | TATGTTTTCTTTAGC[C/T]GTACTGGGACAGAAA | 55130 |
| rs566652532 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27978441 | GAATCCTCAATTTTT[A/C]CCTCCCATGTGCATA | 55130 |
| rs566652601 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27850216 | TTGGGAGGCCAAGAC[G/T]GGTGAATCACTTGAG | 55130 |
| rs566675575 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27838142 | TCCAACGTACTAATT[A/C/T]AAGCACTGTTTACTT | 55130 |
| rs566721802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27824981 | ACATCTCCACTTGGA[C/T]ATAAAAATGACACCT | 55130 |
| rs566740856 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | ARMC4 | GRCh38.p7 | 10:27885877 | TATAAAAATATATAT[A/T]TGTTTGGATATATAT | 55130 |
| rs566754514 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27924886 | TATTAAATAATTTTT[A/T]AAAAAACTGTAGGTC | 55130 |
| rs566777601 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27893910 | ATCCCAGTGCTTTGG[G/T]AGGCCGAGGTGGGTG | 55130 |
| rs566784759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27950086 | CAATCAAGAAGCAGC[C/T]GGTGAGACTTGGAGA | 55130 |
| rs566855422 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27938678 | GATCTTGGCTCACTG[C/T]AACCTCCACCTCCCA | 55130 |
| rs566873728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27988962 | GACAGGAGGGACAGA[A/G]GCAGCGACAGGGATA | 55130 |
| rs566875588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27980705 | GATGTGAAGAAAGTG[A/G]AATCTTTGGATAATG | 55130 |
| rs566880504 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27918962 | ATCACAAAACCACAA[A/G]TAAGTAGATAACTAG | 55130 |
| rs566885162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27986920 | GTGGAAAGGGAGACT[A/G]TTAAAGGCTGTCTCT | 55130 |
| rs566910013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27924179 | AAAAAGTCAACACAC[C/T]CTGATCAAAATGTAG | 55130 |
| rs566917301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27887853 | TTTAAAAAAGTGGGA[A/G]GACCCAAATAACTAA | 55130 |
| rs566918796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27893274 | TATTTTCTTAACACA[C/T]ACATCTGAAAATGTG | 55130 |
| rs566920112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27857534 | CTTTTATCTTTTCTT[A/G]AAGTGTGACTGCTAG | 55130 |
| rs566922576 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27937875 | CATATATACAAATAT[A/T]TACAAGTCAGGGCTA | 55130 |
| rs566933162 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27959772 | TAATAATGAATGCCT[A/G]TAATAGTAGTGAATC | 55130 |
| rs566948711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27986090 | AAGGCATTAACATTC[C/T]CATGTGGTCATGGGA | 55130 |
| rs566957203 | snp | A/T | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27931688 | AAACAGTTATATTAA[A/T]GAGAATTTAAAGACT | 55130 |
| rs566957728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27864378 | AGTGGAACTATCTAG[A/G]ATGCAGATGAATGTA | 55130 |
| rs566969143 | snp | C/G/T | 4.94768e-05 | 0.00497352 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27944353 | TATTCACCATAATTG[C/G/T]TAAGCCCCCAAGGTC | 55130 |
| rs566971137 | in-del | -/GGT | 0.00478085 | 0.0486577 | intron-variant | ARMC4 | GRCh38.p7 | 10:27931315 | CCATTCCCCTGTTTG[-/GGT]GAATATAATTTTTTC | 55130 |
| rs566981359 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872964 | ACTTCTGGTAGCATT[A/C/T]GGCTATGAATCCCTC | 55130 |
| rs567009232 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27992864 | AAATTTGTACAAAGG[A/C]AAAACAATCATGATA | 55130 |
| rs567034272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27904326 | GCGCGGGGAACATGG[C/T]GTCATGGCAGGAAGC | 55130 |
| rs567036577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27988438 | TGCCTCCGGAGCTCA[A/G]GCAATCCTCCCACCT | 55130 |
| rs567059518 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27859679 | GCTATAGAAAAGAAC[G/T]AATATTTTAAATCAA | 55130 |
| rs567059908 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27976631 | GACATACTATGTTCA[C/T]GGATTAGAAAATTCA | 55130 |
| rs567060203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27856743 | AGGCCGAGGTGGGTG[A/G]ATCACCTGAGGTCAG | 55130 |
| rs567071021 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27899421 | CTAGCTGCAGGAGTG[C/T]TTTTTTCATACCCCA | 55130 |
| rs567071259 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27992123 | TACTTTCCATTATGA[C/T]CAAAATCTCAGCTGT | 55130 |
| rs567079519 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27910162 | ATCTTATAAATCCCA[G/T]CAAAATTAATTTTCC | 55130 |
| rs567085451 | snp | C/T | 0.000230943 | 0.0107433 | missense | ARMC4 | GRCh38.p7 | 10:27995096 | AGGATTCCAGTTCCA[C/T]GTCCGGCAGCAGTCC | 55130 |
| rs567103964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27959522 | GTCACCGTGCGTGCC[A/G]GTCTGGACCACTGTG | 55130 |
| rs567109951 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27847009 | ACAAGGAGGAGCGGG[A/G]ACCATTCCTTCTGAA | 55130 |
| rs567122414 | snp | G/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27981975 | GGTTAGAATTTAACC[G/T]TGGAAAAGCCTACAT | 55130 |
| rs567127060 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27817160 | TAATGTAAAAAATAA[C/T]GAGCAGGAAGAACAG | 55130 |
| rs567136677 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27866631 | GCTTCTGGTGAGGGC[A/C]TCAGGAAGCTTCCAC | 55130 |
| rs567141946 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27987638 | ATTATTCCTATATCT[C/T]ATTATAAAATACAGA | 55130 |
| rs567150801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27998653 | CTGGGAGAGAGAAGG[A/G]AAGGGGGCGGGTCTT | 55130 |
| rs567154679 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27892525 | TTAAGCTGGAAAAAC[A/C]TATCTGTTTCACCTA | 55130 |
| rs567159074 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27978435 | ACATCCGAATCCTCA[A/G]TTTTTCCCTCCCATG | 55130 |
| rs567161839 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | ARMC4 | GRCh38.p7 | 10:27812722 | TTTTCAATAGTAAAT[A/T]TTTTTAAAACCACCA | 55130 |
| rs567166696 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27849638 | CTTAAAAAGAGAGGG[A/G]AAAAAGTGGCTTTAA | 55130 |
| rs567209495 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27946521 | ACATCTTTTTTTGTG[A/G]TGGGAACTTTACAAT | 55130 |
| rs567255813 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27971944 | TTATTCAGTCAGGAG[C/T]AATACCATGCCAGCC | 55130 |
| rs567291468 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27964686 | TCAGCAAGAACAGAA[A/T]CAAATCTGTGGTCTA | 55130 |
| rs567293900 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ARMC4 | GRCh38.p7 | 10:27877560 | TTTAAAGATTTTAAA[C/T]ATATGACGTCTTGCC | 55130 |
| rs567317017 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27862778 | TATATTATTTCTACA[A/T]GTATATGTATAAAGT | 55130 |
| rs567322965 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27813220 | CCCTATCTAAAATGC[C/G]TTCCCATCCCCTTCT | 55130 |
| rs567328990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27965351 | GGAGAACAGCTGCTG[C/T]CACTGAAAAGTTTCA | 55130 |
| rs567337023 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27913587 | TATGCAAACTATGCA[C/T]CTGACAAAAGTCTAA | 55130 |
| rs567346032 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27945577 | CAGAGTCTTGCAAAC[C/T]AATGTCTTCTTGGTG | 55130 |
| rs567355714 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27844883 | GAAGGAGTTGGATTT[A/G]ACTTAGCAGAAGCAA | 55130 |
| rs567365575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27838883 | AGCTGCGGGACATAG[C/T]TACTGTTGAACAGAT | 55130 |
| rs567366142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27953135 | CATCACCTGAAAACA[C/T]GTCCTTTGTCTCTGC | 55130 |
| rs567391128 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27851851 | CCAAGCACAAGAAAC[A/C]TGAAGGAAACTACAC | 55130 |
| rs567395253 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27946653 | CTGTATTTTGTACCT[C/T]TTAACCAATTTATCT | 55130 |
| rs567415152 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27825524 | TGCTGCAATGTATAT[A/G]TCCTTCCATCACTTC | 55130 |
| rs567431014 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27907173 | AATCGATTTCAGAAA[C/T]TTCTGGTCTCCTGTT | 55130 |
| rs567432720 | in-del | -/A | 0.0123036 | 0.0774623 | intron-variant | ARMC4 | GRCh38.p7 | 10:27881665 | AAAGAATGAGCCGGC[-/A]AAAATACATCCTTGA | 55130 |
| rs567454291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27832668 | TTCATGAATTACCAG[A/G]GCACACGTGACCAGG | 55130 |
| rs567494182 | snp | C/G | 0.0221141 | 0.102801 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872401 | CACTATGTTGAATAG[C/G]AGGGGTGAGAGAGGG | 55130 |
| rs567496867 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27818826 | TAGTCCATAGCTCAA[A/C]TACCTGAGAAGGAAT | 55130 |
| rs567514074 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27949446 | ACAGGGAAAGAACAT[C/G]TGAACTGAGATCTGG | 55130 |
| rs567518358 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27938007 | GGAGTACAGTGGCAC[A/C]ATCTCAGATCACTGC | 55130 |
| rs567521428 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27972625 | GAAAGCAGGAATGGC[C/T]ATATTAAAATCAGAC | 55130 |
| rs567555226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27938788 | TATTTTTAGTAGAGA[C/T]GGGGTTGCACCATGT | 55130 |
| rs567574579 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27886633 | AGTATTACAGTAATT[G/T]TGTAACTCCACTTTT | 55130 |
| rs567587344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27911575 | AGACAGAAGACACCA[A/G]TTTACTCACAGGCCA | 55130 |
| rs567602188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27925569 | CATTACGTTTTCCAG[A/G]CTGGTCTCAAACTCC | 55130 |
| rs567627627 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27817658 | TATGTTGCTGCAAAA[C/G]ACATGATTCATTCTT | 55130 |
| rs567672559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27910264 | ACACTAGCTAGCACA[C/T]TTGATCAGCGCTTGT | 55130 |
| rs567681010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27979696 | CTGAAAACTTCTAAA[C/T]ATTGCTGAAAGCCAT | 55130 |
| rs567696185 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27832247 | ACACAATGAAACTTA[A/T]TAATCACTCTTTTGC | 55130 |
| rs567718191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27850692 | GTTAAGATGGAGTAA[C/T]GGGGACTGGATTTAC | 55130 |
| rs567723980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27932027 | GCAGCCTCAAACTCA[C/T]GGGCTCAAGCAATTC | 55130 |
| rs567726570 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27899861 | TGGGACAGAACACCT[G/T]GGGGAAGGGGTGGCA | 55130 |
| rs567738041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27978975 | AGCACTTTGGGAGGC[C/T]GAGGCAAGCAGATTA | 55130 |
| rs567761314 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27963299 | AGCATGAGCCACTGC[A/G]CCCGGCCTGTCCCAG | 55130 |
| rs567763622 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27817245 | TATTCACACTTAAAT[C/T]CCTTTCCTAGCTCAC | 55130 |
| rs567816280 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27951776 | TAATGTACAAAAGAG[G/T]AGACAAAAAGACATC | 55130 |
| rs567854041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27894076 | CTTGAGCCCAGGAGA[C/T]TGACATTGCAGTGTG | 55130 |
| rs567887431 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant, frameshift-variant | ARMC4 | GRCh38.p7 | 10:27858213 | TATGCCACACCCACA[-/T]TTTTTTCCTCCTTAA | 55130 |
| rs567891974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27893405 | ACTTAGGTTTCATGA[C/T]GCCTGACAGACGTGG | 55130 |
| rs567895314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27904921 | AGGGATGCTTCTTTG[C/T]TGCTATTATACATGG | 55130 |
| rs567899870 | in-del | -/T | 0.00478085 | 0.0486577 | intron-variant | ARMC4 | GRCh38.p7 | 10:27994179 | TGAGACAGAAGTAAA[-/T]TTTTTTTCATCTCAG | 55130 |
| rs567934724 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27993034 | AATTCTCCTGCCTCA[C/G]CCTCCCTAGTAGCTG | 55130 |
| rs567973353 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27993951 | TGCAAAATAAACTGA[A/G]GCTGGCAAATATATA | 55130 |
| rs567975334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27986160 | GGGAGAGGAGAGCAG[C/T]GAAAAGGAGACAAAG | 55130 |
| rs567979073 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27899456 | TGCCCGGAATGCCAG[C/T]GAGACAGAACTGTTC | 55130 |
| rs567989381 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27964820 | AAGTTCCATAAAGGT[A/G]AGGACCATTTCTGTC | 55130 |
| rs568008849 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27824235 | GTCTAGGAGAACATC[A/T]AATCCTGCTATGGAT | 55130 |
| rs568029165 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27864511 | TGAAGTGAGAGTGGA[C/G]AGTGAGGTGAGAGCG | 55130 |
| rs568040482 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27923960 | TGAAAGAAAGAAAGA[A/T]AGAAAGAAAGAAAGA | 55130 |
| rs568063742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27951206 | AAAAATAATTTATAG[A/G]TTCATGTAAACCAAC | 55130 |
| rs568065530 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27992002 | TCTCTGGTTGACATC[A/T]CTTGTTCTCATAGCA | 55130 |
| rs568089097 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27931480 | AAAATTATCACTTCA[C/T]TTGTCTGTCTACCCA | 55130 |
| rs568110175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27891796 | TTAAGAAAAAATGTT[C/T]CTTACAAATGTTGGC | 55130 |
| rs568116720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27898922 | ACACATTACAATTCG[C/T]TTTTTAAAAAATATT | 55130 |
| rs568131332 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27823531 | AATTAGGATTTTTAA[G/T]AGTACTTTCCTAATA | 55130 |
| rs568153089 | snp | A/C/T | 0.00557806 | 0.0525533 | intron-variant | ARMC4 | GRCh38.p7 | 10:27831101 | GGATCTGGAGGCCAA[A/C/T]GGCCCAGGAGACAGT | 55130 |
| rs568193120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27998030 | GATTGTTTTTCTTTC[C/T]AAAGGTCAATTTCAA | 55130 |
| rs568200680 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27963840 | GCCACAAGAGTTCCG[C/G]ACAACAGACTGTGGG | 55130 |
| rs568210627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27870596 | ACCTATGAGTGAGAA[C/T]ATGCGGTGTTTGGTT | 55130 |
| rs568222423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27882896 | CTTATCCCTAGAGTG[C/T]TTGTTATACAAAATC | 55130 |
| rs568228000 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27876199 | TTTGAAGAGAGTAGT[G/T]GTTCTCCCAGCACAG | 55130 |
| rs568228695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27988380 | TATCCCTCTGTCACC[A/G]GGATTGGAGTGCAGT | 55130 |
| rs568247937 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27862718 | CAGCTGTGAGGTACA[C/T]CTTTGGCATGAAAGA | 55130 |
| rs568252787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27977108 | GATCATAGATATAGA[C/T]TGGAAAGGTAAAATT | 55130 |
| rs568261138 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27928808 | AACAATACTAGCCTA[C/T]ATTTACACACAGCAC | 55130 |
| rs568266706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27883692 | AGGAAGTAGTGTGCA[C/T]CAATAAAGAGAATTA | 55130 |
| rs568267518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27963411 | TGTCAGAGAAATTAA[A/G]AGGAGAAAAAAAATC | 55130 |
| rs568283675 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27849562 | TAATAATAATAATAA[A/T]AAAGAAGTCAGCTGA | 55130 |
| rs568292032 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27955908 | CTGAAGCTGGCAGCC[C/T]GGTGGCATTTCTGAT | 55130 |
| rs568313828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984125 | GACATTGAAAGCATT[C/T]TGCAAATGTAATTAT | 55130 |
| rs568329996 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27842279 | CTCTCTTCCTGAATT[C/T]TGGGGATGGTGAATA | 55130 |
| rs568333674 | snp | A/C | 2.26216e-05 | 0.00336308 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27985011 | GTTCCTTTTTGAAAA[A/C]GACTCACAATGAAAT | 55130 |
| rs568343864 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27844472 | ACTGCAAGCATAGGA[G/T]TCCACACATATATGT | 55130 |
| rs568369741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27977497 | TTGTGAACCCAGGAG[A/G]TGGAGCTTGCAACGA | 55130 |
| rs568452723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27961940 | ACATGGTGGTGCATG[C/T]CTGTAATTTCAGCTA | 55130 |
| rs568453246 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27903022 | GTCAAGCCAATGTCC[C/T]TGATGAACATCGATG | 55130 |
| rs568464315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27943198 | AATGATGGCAAAGGT[A/G]GTAAGCAGGATTCTG | 55130 |
| rs568475036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27904957 | TCTTAAGTCCTTTAA[C/T]ATAAATATTGTTTGT | 55130 |
| rs568486810 | in-del | -/AAAA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27819598 | AAAAAAAAAAAAAAA[-/AAAA]GTTAACCAGACATAG | 55130 |
| rs568503785 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27833962 | CCGAGAAAGGACAGC[G/T]GTGAAGGTTCCACAT | 55130 |
| rs568534155 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27908925 | ATAAGAAAAAATACA[C/T]GTAAAAATTATTTTA | 55130 |
| rs568540271 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27815974 | ACATGAATCTCTTTC[C/T]AAGTATTTTCCTGTA | 55130 |
| rs568545568 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27844873 | GGGTGGTGGCGAAGG[A/T]GTTGGATTTGACTTA | 55130 |
| rs568598039 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27910361 | ATGGTATTAAACCTG[A/C]AATTCCAGAGCTCGG | 55130 |
| rs568634761 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27910942 | ATCAACCAATCAATA[C/T]ATAACGTTGTTTCAC | 55130 |
| rs568698704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27924310 | ACAGGGGAATACAAA[A/G]TGAAATTAAGACACT | 55130 |
| rs568700507 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27897942 | AGGCTGCTTGCATAC[A/G]AGACCAGCCAGATAT | 55130 |
| rs568716001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27821739 | TGGTACAAGTGATTA[C/T]GAAATTGGTATACAC | 55130 |
| rs568728499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27867116 | CAATATACACCATAG[C/T]AGGTGAACAAGATAC | 55130 |
| rs568754822 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27835518 | TGAGTTAGGGCACCA[C/T]GCCCTCATACAGTCA | 55130 |
| rs568767920 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27884630 | TAGATTTCAGCTAGC[A/C]GAAGCTATGAAAAGC | 55130 |
| rs568786887 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27914541 | AGAGCTTTTCTTTCA[C/T]TAACTAGAGCTCAAT | 55130 |
| rs568793540 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27994123 | TGTGTATATATATAT[A/T]TTAGCCATGTTTGAA | 55130 |
| rs568842952 | in-del | -/CTAA | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27858637 | TTTACAGAAACTTTC[-/CTAA]CTGTGTGGGTGGGCC | 55130 |
| rs568846990 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27917496 | GTTAAACACAAATAA[C/G]TACAATAAATAAAGT | 55130 |
| rs568884678 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27977562 | AGTGACAGAGGGAGA[A/C]TCTGTCTCAAAAGAA | 55130 |
| rs568889074 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27952458 | GTTTGTTACATAGGT[A/C]AACGTGTGCCATGTG | 55130 |
| rs568897250 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27952296 | TACATTTTGCCCCTG[C/T]GAGAATTGGCCAAAA | 55130 |
| rs568897505 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27817747 | CTCTATGAATGGGCA[C/T]TTAGGTTGATTCCAT | 55130 |
| rs568902878 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27883963 | CCAACATACACATAT[A/G]AGCATTCTAGAAAAA | 55130 |
| rs568930040 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27951278 | TCAACTCATTCTAAA[A/G]ATGATCTAGAATGAA | 55130 |
| rs568932288 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27912739 | TTAAAAGAACATGAC[A/G]TTCTTAAACCACAAC | 55130 |
| rs568935189 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27960461 | AAGCAATTCTCCTGC[C/T]TCAGCATCCCGAGTA | 55130 |
| rs568942576 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27971714 | ATAAGAATTTTAAAA[C/G]ACTTCTCATCAGAAA | 55130 |
| rs568975484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27832016 | GTCAAGCATATTCGG[A/G]GCTTCCCCTGAAGGC | 55130 |
| rs569001673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27924764 | AAATAAATTTGAAAG[C/T]TGAAAGGAAATTGAA | 55130 |
| rs569013260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27871056 | GACATTCTAACTGGT[A/G]TGAGATGGTATCTCA | 55130 |
| rs569028120 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27923529 | CATTAATAATAAGAG[A/C]ATTTCATACAGCAGT | 55130 |
| rs569045287 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27856684 | CTGGTGCAAACCGAG[A/T]CATACTAGAAAACAC | 55130 |
| rs569047328 | snp | C/G | 0.000310029 | 0.0124466 | missense, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27985065 | GGTGCAGATCCAATT[C/G]CTTAAGCAGCATAGC | 55130 |
| rs569081941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27863474 | GTGCATGTCCAAGAA[C/T]GACCATATTGAGTAG | 55130 |
| rs569089782 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27956851 | CAACATTTTACCCCA[C/T]TCTACTGAAGAATAC | 55130 |
| rs569118267 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27934449 | TATGAATATATATCT[G/T]TATATAGATATATTT | 55130 |
| rs569118554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27862894 | GGAGAGTCACTGTGT[C/T]AGCTACTGAGGATAT | 55130 |
| rs569119907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27850176 | TTTGCTGGGCGTGGC[A/G]GCTCACACCTGTAAT | 55130 |
| rs569140082 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARMC4 | GRCh38.p7 | 10:27924001 | GAAAGAAAGAAAGAA[A/G]GAAAGAAAGAAAGAA | 55130 |
| rs569141791 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27931509 | CAGCTCAATCAGGTC[C/G]TTCAGGCTTGTTGTT | 55130 |
| rs569149896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27837503 | GGTCTAGAGAAAATA[C/T]CAGCGTTTTCAGTCA | 55130 |
| rs569180650 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27852952 | GGTGACAGAACGAGA[C/T]ACAGTCTCAAAAAAA | 55130 |
| rs569180959 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27886411 | ACTGAACATTCGATA[C/T]TGATCAAAACTGTCT | 55130 |
| rs569188587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27837029 | TAAACTGCCCACCGT[A/G]AGGATTTCTGGGACT | 55130 |
| rs569191848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27994100 | TTCACATAATTTATG[C/T]GTATGTGTGTGTATA | 55130 |
| rs569210122 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27891778 | TTAAAAATGCACTGA[C/T]ATTTAAGAAAAAATG | 55130 |
| rs569248933 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27898517 | TAAATATATAGTGAT[A/C]TTTGTTTAAATTTAT | 55130 |
| rs569251887 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27963243 | CGAACTCTTGACCTC[A/G]TGATCCTCCCGTCTC | 55130 |
| rs569268913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27937196 | CACTAGCAAGGAATG[A/G]AGGATTTCTGCAGTG | 55130 |
| rs569298999 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27913806 | TCACATGAGTCGGAA[A/T]GGCTATTATGAAAAA | 55130 |
| rs569327654 | in-del | -/CT | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27947188 | TGAATTTTAAAAATC[-/CT]CTCTTTATAACTGTC | 55130 |
| rs569329391 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27918656 | AACATATATGTTTGC[A/T]CTCATTTGATTGTAA | 55130 |
| rs569329935 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27949165 | TGCCTCAAATCACTT[C/T]TGTGTTATTTCATTC | 55130 |
| rs569330300 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27980954 | GATGAATGCATAAAC[C/T]AAATGTGGTCTATAC | 55130 |
| rs569331278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27992032 | AAACACTGAGTGGCT[A/G]TGGGTTACTGAACTT | 55130 |
| rs569332857 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27949692 | TATTTCAAGATTGGC[C/G]AATGTAATTTACAAT | 55130 |
| rs569344031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27817045 | ATGAGCCACCGTGCC[C/T]GGCCTGTTATGCAGT | 55130 |
| rs569349127 | in-del | -/AGATTACAAAGATAA | 0.00597247 | 0.0543191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27921708 | CCTAGCAAAATTATT[-/AGATTACAAAGATAA]AAATCCCCAGTCCAA | 55130 |
| rs569367307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27899053 | AGCTCTGGTCTGCAG[C/T]TCCCAGTGAGATCGA | 55130 |
| rs569370526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27943300 | AAGACAAATTGGCAA[A/G]TGTAGAAATGCAGGC | 55130 |
| rs569380283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27823357 | AAAGTGTAGATGGCA[A/G]TTCTCTGGAAAAAAA | 55130 |
| rs569394473 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27998600 | CCCCAACCTAGGGCC[A/G]AGGCAGGGTCTCGCG | 55130 |
| rs569433164 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27903438 | CAATATAGTATTGGA[A/C]GTTCTGGCCGGGGCA | 55130 |
| rs569443366 | snp | A/G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27836930 | GCAGTTCACGACTAA[A/G/T]CCTCAAAGATATAAA | 55130 |
| rs569464802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27842035 | CACTTTCCCTCTGGC[C/T]GCAAATTCTTCTCCT | 55130 |
| rs569503650 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27814908 | TCAGTTCAACCTCAA[A/C]TGGATTCTCATTCAC | 55130 |
| rs569539379 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27821551 | AACTAGCAAATACTC[A/G]CACAACAGAAAGTTG | 55130 |
| rs569547518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27935823 | GTGTGCATACATATA[C/T]ACACACACATATGTA | 55130 |
| rs569561627 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27865782 | ACAAACCAAACTAAA[C/T]TCCTACTAAATGGTG | 55130 |
| rs569567540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27815109 | CAACTCTACCTAAAA[C/T]GGCAACCATGCCAGC | 55130 |
| rs569580668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27869714 | TAATTTTTGTATTTT[C/T]AGTAGTGACAGGGTT | 55130 |
| rs569590928 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27923210 | AAAACAAAAACTATG[C/T]TTAATTGACTCACAA | 55130 |
| rs569591669 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27908987 | CTAAAACTTTCATAC[A/C]ATGCTGAGAGAAAAC | 55130 |
| rs569599588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27914570 | ATTACAGTTTCTCCA[C/T]AAAGGCAGAATATAT | 55130 |
| rs569600249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27969505 | TATTTTAAAACTCAC[C/T]TGCCAGTTAAAAAAG | 55130 |
| rs569603147 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27884227 | CTGACTTTTCATCAG[A/G]AAGTGTAGAGATGTT | 55130 |
| rs569635965 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27843716 | CAGATGCAATGAGCC[A/G]AGATCACACCATTGC | 55130 |
| rs569641160 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27838862 | GGATCTTTTATCAAC[-/A]AAAAAAGCTGCGGGA | 55130 |
| rs569682410 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27922307 | TTCTGCACCCCTGAG[C/T]CCTTTTTGAAGATTC | 55130 |
| rs569686650 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27882660 | ACTTTCTCTATTCCA[A/G]TCTCCCTCTCTCCAG | 55130 |
| rs569697850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27969203 | TTTCAGCACAGCCCT[A/G]TGTTTTACATATTGA | 55130 |
| rs569723107 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27881946 | TGAAGTGGGCAGATT[C/G]CTTGAGCCCAGAAGT | 55130 |
| rs569733669 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27838673 | ATCTGCCAGATTCCT[C/T]GACTTTTTGGCACAC | 55130 |
| rs569740572 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27813906 | GAAGGAACAAATTCA[A/T]GCGATATTTGGGATG | 55130 |
| rs569760489 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27976095 | TAAAATCCAACATTC[A/T]TTCCTAATAAAAGTT | 55130 |
| rs569792015 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27848430 | ATTGATTCAAGATGG[A/G]TTAAAGACCTAAAAC | 55130 |
| rs569802190 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27897546 | CATCCACACTGCCAT[A/G]GTGTTAGGTCAAATT | 55130 |
| rs569822076 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27863424 | GCCTCAGCTGAGAAC[A/G]TGTGCATTGGACGAC | 55130 |
| rs569834549 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27913781 | ATCAAAACCACAAGA[A/C]GATACTATCTCACAT | 55130 |
| rs569849847 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27848123 | TGCCATGACAATCCT[A/C]AGCCAAAAGAACAAA | 55130 |
| rs569860327 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27890816 | GTTACTCTAATCTTT[G/T]AGGATTTTAGGATCT | 55130 |
| rs569884467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27896991 | CTCTCAGTGGAAATG[A/G]CTACAACCACGACCG | 55130 |
| rs569929415 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27942869 | GTCTATCTCATTTTT[G/T]AAACAAATACATTTA | 55130 |
| rs569931983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997492 | GGTAGTCAACATACC[A/G]TATAGTAACTTCTTG | 55130 |
| rs569936701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27880055 | ATGGTAGTTCTGCTG[A/G]TGTGGCAAACTCCAT | 55130 |
| rs569964091 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27854865 | AGCCACATAAGAATG[G/T]GAATTAATACGAAAA | 55130 |
| rs569965241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27902731 | TGGACACATACACCC[C/T]CCCAAGTCTAAACCA | 55130 |
| rs569967801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27947934 | TTTTCGAGCTTATAC[A/G]CTCAGCACAATCTTT | 55130 |
| rs569972484 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27888455 | ATATTCCTGTTGGCT[A/G]TTTGTACGTCTTCTT | 55130 |
| rs569976252 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27912837 | TAAATGTATGTCAGA[A/C]TTAAAATGATCATCC | 55130 |
| rs570000929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27854412 | TTGTACATGAATGTT[C/T]GTAGCAGCTTTATTT | 55130 |
| rs570003158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27861726 | TATACGTAATTGCCC[C/T]GTAATGGGCATACTA | 55130 |
| rs570020140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27820303 | GTTTCGCCCATCCTC[C/T]CTCAGACCTGGTCAT | 55130 |
| rs570043321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27868405 | CGCAGCACTATTCAC[A/G]ATAGCAAAGCCATGG | 55130 |
| rs570044173 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27954919 | ATACTACAATATCTA[A/T]GAAAGCATAAATGCA | 55130 |
| rs570062461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27820876 | CAACCTCTGACTCCC[A/G]GATTCAAGCCATTCT | 55130 |
| rs570097722 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27919375 | GGTTTCTGCTCAAAA[-/G]GAAGTCTTAATGCTT | 55130 |
| rs570117158 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27967062 | AGGCAAAAAAAGGAC[C/T]TAAGAAAGTCCTGCT | 55130 |
| rs570133366 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27873726 | GTCTGAGAGACAGTT[C/T]GTTATAATTTCTGTT | 55130 |
| rs570161603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27822854 | TTATTGGATCCAGTG[C/T]TCTTTCTGTGTGGAC | 55130 |
| rs570178679 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27874314 | CTCTTTACCCACTTT[G/T]CCAGTCTGTGTCTTT | 55130 |
| rs570192245 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27922357 | AAACTAAGACTATAG[A/C]ACTTAAGCTAATTGA | 55130 |
| rs570198069 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27830469 | TAGATAGCCTTGCTT[A/C]ATCTTCCCAGATTTA | 55130 |
| rs570206953 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27954243 | GGGAACCAGCCAGTA[C/T]CACTACTCTTCTCCA | 55130 |
| rs570211100 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27867867 | GGCATGAGAATCGCT[G/T]GAACCTGGGAGGCAG | 55130 |
| rs570235942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27967719 | AACATGGCAAAACCC[C/T]GTATCTACTAAAAAT | 55130 |
| rs570253066 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27945317 | GGGTATTGCATAATG[C/T]AAAGCACGTCTGAAA | 55130 |
| rs570281002 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27878287 | ATTGCACAAATAAGA[C/T]GAAAAATATAAAACA | 55130 |
| rs570289008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27879198 | ATGCCCTGGGTTGAT[C/T]CTGCTTTAGATGCAG | 55130 |
| rs570303214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27926656 | ACTTTTCCATAAGTC[C/T]AATGCTATTTCAAAG | 55130 |
| rs570319529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27973639 | TTTTATGGCTGTGTA[A/G]TATTCCATGGCATAT | 55130 |
| rs570328881 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27916248 | CATACTAGGGGAAGG[A/T]GGCCTAACATGGGGA | 55130 |
| rs570338067 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27934352 | TCACCCAGGTTCCTC[C/T]TTTGTTGGAGTAAAG | 55130 |
| rs570348654 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27847409 | CAATAAATTAGGTAT[C/T]GATGGGACGTATCTC | 55130 |
| rs570378393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27840468 | CCTCCAATGGCAAGT[C/T]TTGGAAGCCATCTTG | 55130 |
| rs570401856 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27877810 | TAATAACAATGATAG[A/T]AAAAATAACAGGCTA | 55130 |
| rs570404856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27883497 | AATGTGATACATACA[A/G]CAAAGGAGAAAAGTA | 55130 |
| rs570413594 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27903336 | TGACAAACCCACAGC[A/C]AATATCATACTGAAT | 55130 |
| rs570414013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27963302 | ATGAGCCACTGCACC[C/T]GGCCTGTCCCAGGCA | 55130 |
| rs570438510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27870452 | GTTGGTGTGCTGCAC[C/T]CATTAACTCGTCATT | 55130 |
| rs570440873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27836871 | ATGGTGTTGAAACAC[A/G]GAGGACTTATTTCAT | 55130 |
| rs570444975 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27993511 | AAAAATTAGCCAGGC[G/T]TGGTGGCGGATGCCT | 55130 |
| rs570453583 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27837487 | CAATCAGAAAATCAT[A/G]GGTCTAGAGAAAATA | 55130 |
| rs570475363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27876040 | AGTAGGTAAACAAAG[A/G]GGCCAGGAAGCTCGA | 55130 |
| rs570477198 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27869790 | TCCACCTGCCTCGGC[C/T]TCCCAAAGAGCTAGG | 55130 |
| rs570578117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27843745 | GCACTCCTGCCTGGG[C/T]GACAGAGCAATACTC | 55130 |
| rs570609609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27970198 | TAGCATTGGCCCTCA[A/G]TTTTTGCTTTGACGC | 55130 |
| rs570614059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27882746 | TGCAGCCTACAAACC[A/G]TAGGAGGGACAGAAT | 55130 |
| rs570618618 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27891019 | CATGGCTAAATCAGA[G/T]CTTGTGTTTATAGCA | 55130 |
| rs570631111 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997518 | TCTTGAAGGACCCTT[A/C]ACACAGAATTAAGAA | 55130 |
| rs570640684 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27868379 | AAAGACACATGCACA[C/T]ATATGTTTATCGCAG | 55130 |
| rs570650665 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983582 | CAGTGAAGTGATTAC[A/G]TTAAAGACATTTATA | 55130 |
| rs570652841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27891604 | TAAGGAAATGGTGAT[A/G]ATACATTAATATGAA | 55130 |
| rs570667778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27977439 | AGGCGCGGTGGCGGG[C/T]GCCTGTAGTCCCAGC | 55130 |
| rs570670018 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27969703 | GTGATTCCCAGAATC[C/G]CTGCAGGAGAAGGTC | 55130 |
| rs570693736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27943118 | AACAGCTCTGGGTGA[A/G]ACACAAGATCTATTG | 55130 |
| rs570714655 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27990534 | AACATAGAAAATAAG[G/T]CTATAGCTAAGAAAC | 55130 |
| rs570728324 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27936585 | TTCTATTCTAAGAAT[A/C]CCTTCATTGGGCTAA | 55130 |
| rs570749370 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27848942 | AATAGGAACACTTTT[A/C]CACTGTTAGTGGGAC | 55130 |
| rs570757745 | snp | C/T | 0.000132188 | 0.00812874 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984005 | TCATCAAGCAATTAA[C/T]AGGAGTTCCTTAACC | 55130 |
| rs570761123 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27880936 | TCATAAAGATTTCTA[C/T]GTGAACCCAATGTTT | 55130 |
| rs570785848 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27855598 | TAGGTGACCTTAGTA[C/T]CTAAAATCCGTTTAC | 55130 |
| rs570852958 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27815229 | TTCTTCTTAGGACAT[G/T]TTACTACCAAATACT | 55130 |
| rs570855663 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27948860 | ACATTCCTTCTGATG[A/T]CCAGGAGGCATTTCT | 55130 |
| rs570891769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27949560 | ACGCAGGGGAGTAGA[A/G]CATGGCATGCTTAGC | 55130 |
| rs570901136 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984435 | ATAATTTTATAACAG[C/T]ACTGTCAACACATCA | 55130 |
| rs570905719 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27988636 | AGCTACCACACCTGG[A/C]CTGATCTAACATATT | 55130 |
| rs570918567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27974938 | TTTTGTAATTCTCAC[C/T]GTAGAGATCTTTCAC | 55130 |
| rs570924184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27821696 | TACATAAAAGGAATA[A/G]TTTTCTCAGGAAAGT | 55130 |
| rs570937784 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27868524 | GAATGAGATCATGTT[C/T]TTTGCAGGGACATGG | 55130 |
| rs570944429 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27817679 | ATTCATTCTTTTTTA[C/T]GACTGAGTAGGCATT | 55130 |
| rs570948208 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27908472 | CCAGGAGCATAACCT[C/T]GCAGTAAGGTCCATT | 55130 |
| rs570994689 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27899286 | ATACTCTGGCCCAGA[C/T]ACTACACTTTTCCCA | 55130 |
| rs571005591 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27828992 | TTATTAGAAGAAATT[C/T]GAAACCAAAGACAAG | 55130 |
| rs571014825 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27979211 | TGGGTGACAGAGTGA[A/G]ATGGAGTGAGACTCC | 55130 |
| rs571030822 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27869670 | CTCCCAGGTAGCTGG[A/G]ATTACAGGTGCATGC | 55130 |
| rs571074364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27852955 | GACAGAACGAGACAC[A/G]GTCTCAAAAAAAAAA | 55130 |
| rs571078853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27955002 | AAACAAGCAATTAAA[A/G]AAAAGTCACAAAAGT | 55130 |
| rs571104712 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27921613 | GGATTTTTTTTTAAA[A/T]AAAGGAGGAATAAAT | 55130 |
| rs571106455 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27967763 | GAGTGTGGTAGCGCA[C/T]GCCTGTAATTGCATC | 55130 |
| rs571111808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27834875 | TCCAAAGAAATTGCC[C/T]GGAAGCTCCGATTTT | 55130 |
| rs571127445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27991397 | ATTAATAACGATCTG[C/T]ACAAAAGGACAGAAG | 55130 |
| rs571139853 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27928376 | TATTTTTATTACATT[A/T]TATTTTATAGGGTTA | 55130 |
| rs571167477 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | ARMC4 | GRCh38.p7 | 10:27953240 | TATAGGTATTATGTT[C/G]TACAGCAGATATCTG | 55130 |
| rs571172149 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27843371 | GAATGCAATTGTAGC[A/G]GATGGTGTAGTGTAC | 55130 |
| rs571211576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27889593 | CTCCACAACCTCAAA[A/G]TCTCTGCAGTCCCAC | 55130 |
| rs571219331 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27896239 | TCAATAAATGGAAAT[A/C]TCTTCCTTATTACCT | 55130 |
| rs571222736 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27941148 | CTTCCCTAAAACCAT[C/T]AGCACTTTCTAAGGA | 55130 |
| rs571243256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27847437 | CTCAAAATAATAAGA[A/G]CTATTTATGACATAC | 55130 |
| rs571248509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27896750 | ACTCTTTCTAGATAC[A/G]TAGATATATGTATAT | 55130 |
| rs571251429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27989095 | TCTCCTTAAGCCTCC[A/G]GAAGGAATGCAACCC | 55130 |
| rs571259883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27934477 | TTTATTTATATATGG[A/G]TATATCTCTCTATAT | 55130 |
| rs571264531 | snp | A/G | 4.95282e-05 | 0.00497611 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27935225 | TAGAAGTCCCACCAA[A/G]GTTTCAATGGCTTTG | 55130 |
| rs571312458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27996090 | TAACGTTAAATAAGA[A/G]CCAAGTTAGAAAGCA | 55130 |
| rs571326330 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27941654 | ATCTTAAGGGAAAGG[A/C]AATTTACTATAAGGA | 55130 |
| rs571343942 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27943588 | GCTCAGGAGTTCAAG[A/C]CCAGCCTGACCAATA | 55130 |
| rs571345384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27833420 | ACTTCTCTAGCAGCA[C/T]GGAAAATACAGCATT | 55130 |
| rs571347275 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27825935 | CACCTCATCCTCATA[A/G]AAAACAAACAAGACA | 55130 |
| rs571378387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27925737 | CTAAGGTTATTCTTT[C/T]ACTTCATAGAGAGAC | 55130 |
| rs571384246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27832813 | TATACTAAAGCTCTC[A/G]TGGGTTAGAACTAAA | 55130 |
| rs571384979 | snp | G/T | 1.67444e-05 | 0.00289343 | intron-variant | ARMC4 | GRCh38.p7 | 10:27860577 | TAAGTTTCTTTCCAG[G/T]CTACATTTACCAAAC | 55130 |
| rs571399483 | in-del | -/CT | 0.00795532 | 0.062565 | intron-variant | ARMC4 | GRCh38.p7 | 10:27875459 | TTTTCAGCTTTTCTG[-/CT]CTGTTTTTCCCCATC | 55130 |
| rs571412775 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27813759 | TACTCAGGGGAATGA[C/G]ATGATCATATTTGTA | 55130 |
| rs571415550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27819608 | AAAAAAAAAGTTAAC[C/T]AGACATAGGTGTGGT | 55130 |
| rs571416348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27926458 | TACTTACAAATTAAC[C/T]GGACAAAAATAAACA | 55130 |
| rs571426315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27906962 | GCATGTGTATACCTA[C/T]GTAACAAACCTGCAC | 55130 |
| rs571428336 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27901201 | ACCCAGAGTTTCATA[G/T]CCAGCCAAACTAAGC | 55130 |
| rs571435964 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27912476 | CTTGTTATGTTAACA[C/T]TTTCCAGGACTGCTA | 55130 |
| rs571441238 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27941325 | CCTGTTTCCACTGGA[-/A]AAAAAAAAAAAAAGC | 55130 |
| rs571478409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27960349 | TATTATTATTATTAT[C/T]ATTATTATTATTTTG | 55130 |
| rs571489157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27867357 | TGATGGTGCTGGGGT[A/G]TTCTGTTAGGCCTGA | 55130 |
| rs571492351 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27849928 | GCTGCTCTAATTGCA[A/G]TAGGTGAACCACCCA | 55130 |
| rs571492376 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27825375 | ATAAAACCTTTCTTT[C/G]TCTTCAAGGGGAGAC | 55130 |
| rs571503574 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27908990 | AAACTTTCATACCAT[C/G]CTGAGAGAAAACAGT | 55130 |
| rs571533933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27966091 | TTTGTAAGATTCCAT[A/G]ATTCTCTTAATTTCT | 55130 |
| rs571541114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27932827 | TTTTATTTGCTAACT[A/G]ATTGAATGTATAGTC | 55130 |
| rs571550544 | in-del | -/AA | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27962184 | CAGTGAGAAATAAAC[-/AA]GGGTATTCAGTGAAT | 55130 |
| rs571556213 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27852370 | TATAACACTTGTATG[A/T]TAAAAATAGCATAAA | 55130 |
| rs571571287 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27959610 | GGCCTGAATCTAGCC[C/T]GTGCTCCATGCTAGT | 55130 |
| rs571575009 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27859942 | GCCAGTTCCTTTGGT[A/G]TTTAGTTGGTGCCTA | 55130 |
| rs571576863 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27830929 | TTTTTCTCTAGTACA[C/T]CTTTTGGATAAGTTT | 55130 |
| rs571599370 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27919344 | CAACCGAAAAATTGA[C/T]CTTCCTCATATTAAA | 55130 |
| rs571668806 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27887610 | AAAAATAAAAAATAT[A/T]GAAGTCATATAAAGT | 55130 |
| rs571671064 | in-del | -/A | 0.00119737 | 0.0244387 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:28000989 | CAGTGACATAATCAT[-/A]AAGCATAGCTCACTG | 55130 |
| rs571691269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27840226 | TTTGTACATATTTAC[A/G]TACATCTTTAAAACA | 55130 |
| rs571700894 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27974225 | CTCCCATTCTGTAGA[A/T]TGTCTGTTTATTCTG | 55130 |
| rs571708340 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27961390 | GTTGCTCCATGAGGA[A/T]GAATCTTGCATCCTC | 55130 |
| rs571724043 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27918776 | AGATTATGTATTTCT[A/G]CATGTAGAAAACCCT | 55130 |
| rs571724340 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ARMC4 | GRCh38.p7 | 10:27842010 | TCCTACCCTATGGCC[A/G]CTGAACAAACACTTT | 55130 |
| rs571777074 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27895035 | AGACTCACTAGTCAT[C/T]GGTACGAAAAAAAAA | 55130 |
| rs571795545 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27875819 | AGCTGTGAGAGATGG[A/C]ACCTGGAAAATCGGG | 55130 |
| rs571804033 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27945566 | CTGGCTGAACGCAGA[A/C/G]TCTTGCAAACCAATG | 55130 |
| rs571817742 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27972674 | AATAATATTAACAGG[C/G]ACGAAGAGGAGCACA | 55130 |
| rs571840618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27841584 | TATTTTTAGTAAAGA[C/T]GGGGTTTCACCATGT | 55130 |
| rs571843444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27979787 | TAAGATGGCAATACT[A/G]TGTAAAGCAATTCAT | 55130 |
| rs571861496 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27887020 | AAAAATAAGTGCTTT[A/C]CTATACTTTAAATGT | 55130 |
| rs571881000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27900511 | AGTAATAACAAACTC[A/G]TCTGAGCTAAAGGAG | 55130 |
| rs571882208 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27980465 | AATATTGGGTATATA[A/C]AAAAACTACAACAAC | 55130 |
| rs571965264 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27987051 | TGTCATCTGTCTTCT[C/T]TATTGACACTGACCT | 55130 |
| rs571969297 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27851582 | AGGCAAATTAAACAT[G/T]GCAGAAAAAAAAGTG | 55130 |
| rs572002107 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27979139 | CACTTGAACCCGGGA[G/T]GGGAGGTGAAGGTTG | 55130 |
| rs572002813 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27847160 | CCTGATGAACATTGA[C/T]GCAAAAATCCTCAAT | 55130 |
| rs572025959 | snp | A/T | 0.14933 | 0.228835 | intron-variant | ARMC4 | GRCh38.p7 | 10:27827380 | TACACACACACACAC[A/T]ATATATATATATATA | 55130 |
| rs572041359 | snp | A/G | 0.0501905 | 0.150254 | intron-variant | ARMC4 | GRCh38.p7 | 10:27846751 | GGGGATATCACCACC[A/G]ATCCCACAGAAATAC | 55130 |
| rs572051587 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27949630 | AAGATGAGCTGAAAA[C/T]CAGCTGGGCTGCTGG | 55130 |
| rs572095571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27870462 | TGCACCCATTAACTC[A/G]TCATTTACATTAGGT | 55130 |
| rs572101603 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | ARMC4 | GRCh38.p7 | 10:27860011 | ACACTATAGCCAATA[C/G]AATTGTGAGTACTAC | 55130 |
| rs572132398 | snp | A/C | 1.70148e-05 | 0.00291669 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940020 | TTCCTAGGAATAAAA[A/C]CCTACATATTTATGT | 55130 |
| rs572145976 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27933959 | CCACCCAAATCTTAT[A/C]CTGAATTCCCACGTG | 55130 |
| rs572157723 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27982024 | GTTCTTCTGTCTGTG[C/G]CATGGTTGCTATAGG | 55130 |
| rs572173938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27920474 | ATGTGGAAAAATAAA[A/G]CCCACATAATCTTCA | 55130 |
| rs572179011 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27887220 | AGATTGTCCATACCA[A/G]TAACAGACAAAATAG | 55130 |
| rs572189760 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27818986 | AACCTCTTAACCCAA[A/C]CTTCTCATATGTGTA | 55130 |
| rs572231699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27934608 | TCATCAGTTCACAGT[C/T]CTTGCCAGGTGCTCA | 55130 |
| rs572265577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27825251 | GAGCCACTACTATCT[C/T]TTGAACTGAATTTAA | 55130 |
| rs572285605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27894860 | GTGAGCCACTTTGCC[C/T]GGCTTCAAATGAAAT | 55130 |
| rs572312642 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27963371 | CAAAGCAGGCTCTAT[C/T]ATCCCCATTCTACAA | 55130 |
| rs572316582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27813343 | TTCCTCATCAGGCTG[C/T]CAGTAGCAGTTTACT | 55130 |
| rs572319767 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27852229 | AAATCTGCATTTACA[C/G]AAAGGAATAAATAGC | 55130 |
| rs572342266 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27895816 | AATGTGCTTTCTTTC[C/G]TCTTGCCTTTCTGAG | 55130 |
| rs572359687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27906500 | ATTTTACCTGCCAAT[C/T]CCATTATTGGGTATA | 55130 |
| rs572361018 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27901313 | GAGCTCCTGAAGGAA[C/G]CACTAAATTTGGAAA | 55130 |
| rs572367720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27925127 | TATTATTACAAAAAT[A/G]CTAAATATTAGCTAA | 55130 |
| rs572377472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27860001 | TGTTAAGTAAACACT[A/G]TAGCCAATAGAATTG | 55130 |
| rs572398951 | snp | G/T | 1.70052e-05 | 0.00291587 | intron-variant | ARMC4 | GRCh38.p7 | 10:27812653 | AGGAGGAGAAGAAGG[G/T]ACACAAGAATAAAAA | 55130 |
| rs572423828 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27900725 | ATCAGATATTGAAGG[A/T]CATCTTAGTGAAATA | 55130 |
| rs572431858 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27973069 | CTTAATACATTGGAA[-/T]TGAACTAGAAATTAG | 55130 |
| rs572443696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27988028 | AAAAAAAAGCAAACT[A/G]AAGGCAAACTAGATC | 55130 |
| rs572463217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27906021 | AATTGACAAATGGGA[C/T]TGAATTAAACTAAAA | 55130 |
| rs572470779 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27823296 | GGATTAAAAAAATCT[A/G]TGTGGATAAGATTGT | 55130 |
| rs572485187 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27952857 | CTGTAAGGAGCTATG[A/C]AACTTTTTTTTACAT | 55130 |
| rs572499364 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27891500 | GATTTGGAAGACATA[C/T]TGAGTTTTCTTCCTA | 55130 |
| rs572559654 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27931084 | GTCTTCACTTCTTCC[A/T]AGACCCATTCAATTC | 55130 |
| rs572612463 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27877803 | CCCTTAATAATAACA[A/G]TGATAGTAAAAATAA | 55130 |
| rs572614691 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27889408 | GCATATCAAATTTGA[C/T]ATCAGAATAATTCCT | 55130 |
| rs572625140 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27878506 | ACTTTAAAGCACATA[A/C]AAGGCGAGCGTAACA | 55130 |
| rs572632018 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27900064 | ACCTTATATAGGAGA[G/T]CTCTGGCTGGCATTT | 55130 |
| rs572639878 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27911160 | GGGACCATATTAAAA[C/G]AGCAAAATCACCATC | 55130 |
| rs572642688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27965682 | TATCTGGGTCCCCAG[C/T]AATCCATAAAAGGGT | 55130 |
| rs572643571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27832389 | TAAGATTATTCCTAG[C/T]GCCAACCCTAGAAGC | 55130 |
| rs572643611 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27971794 | GAAAACACAAAAAAC[C/T]ATGTCAACCCAAAAT | 55130 |
| rs572659217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27865837 | ATGCAAGTGTGAGGG[C/T]GAAGCCACTTTCTCT | 55130 |
| rs572661537 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872522 | CTTATTATTTTGAGA[C/T]ACGTCCCATCAATAC | 55130 |
| rs572681927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27838535 | ATTACAAGAAGCTGC[C/T]GGTGTATTTCTGTGG | 55130 |
| rs572695933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27917170 | TGAAAGAACTGAAAT[C/T]ACATATAATATCATC | 55130 |
| rs572702125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27871985 | GATTCTTCCTATCCA[A/G]GAGCATGGAATGTTC | 55130 |
| rs572703901 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27979223 | TGAGATGGAGTGAGA[A/C]TCCATCTCAAAAAAA | 55130 |
| rs572738396 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27869279 | CAAATAGGCAGAGAA[A/G]ATCTAACACATGTAT | 55130 |
| rs572742214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27993245 | TTTTAATTTGTTTTA[C/T]GTAGGAGATCATATT | 55130 |
| rs572761495 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27992093 | CGGTCAAGACCTGGA[C/T]GTTAAAGCATCTGGT | 55130 |
| rs572766987 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | ARMC4 | GRCh38.p7 | 10:27998822 | AGCACCCTGCCCCCC[G/T]CAGTCGGCGCCCGCC | 55130 |
| rs572777796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27932359 | TAGAGGTACTTGAAG[C/T]ATAGTTTCTACTGAC | 55130 |
| rs572781576 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27989520 | GCTGGCCACCACACG[A/G]AGTGGATGGTGAGAG | 55130 |
| rs572786480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27931826 | AGAAGTAGAGGCTTC[A/G]CAAGAGTAAGTTCTA | 55130 |
| rs572804057 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999421 | TAGGGCTTCTCCTAG[C/G]ATATTTGAGGCTTAC | 55130 |
| rs572831163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27885048 | GGAAAGCATGGCTTA[C/T]GTAAGGGAACAAATC | 55130 |
| rs572847199 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27938275 | CAGAGTTTTTAAAGA[G/T]GTCATTAAGGCTAAA | 55130 |
| rs572848812 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27871091 | GGTTTTGATTTGTAC[C/T]TCTCTGATGGCCACT | 55130 |
| rs572900819 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27958626 | AGGCCACCTGCACGA[G/T]TCAGTTAAGTCTCCA | 55130 |
| rs572924819 | in-del | -/AT | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940238 | CAGCATATATGTGTG[-/AT]ATATATATATAAATG | 55130 |
| rs572925599 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27945040 | GTAGTTACGAATCCA[G/T]GAACTGGAAAACATG | 55130 |
| rs572932063 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27857780 | CTAACAAAGCAGCTA[A/C]TCCTAGGATCAATTA | 55130 |
| rs572947643 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27876250 | ACAGACTGCCTCCTC[A/T]AGTGGGTCCCTGACT | 55130 |
| rs572961438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27875841 | AAAATCGGGTCACTC[C/T]CACCCTAATACTGCA | 55130 |
| rs572971132 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27874662 | GAAAATTCTTTTCTT[C/T]AAGAATGTTGAATAT | 55130 |
| rs572980475 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27829396 | TCCCGTTGACTTAAC[C/T]TCATTCTCAAGGCCT | 55130 |
| rs572992940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27977670 | TATAAGCCAAGAACA[C/T]ATATAAAGATCTGTT | 55130 |
| rs573017088 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27850361 | GAGGCAGGAGAATGG[C/T]GTGAACCTGGGAGGC | 55130 |
| rs573029783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27844650 | AAGATAATAAGTTTC[C/T]AACTCAATAGGTTAT | 55130 |
| rs573071805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27910484 | ACTTGGGTCAGGCAC[A/G]GTGGCTCACGCCTGT | 55130 |
| rs573073071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27909765 | GGAGGTTGCAGTGAG[C/T]CGAGATTGCACCACT | 55130 |
| rs573085216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27848786 | CATTTATGAAGCCAA[C/T]AGACACACGAGAAAA | 55130 |
| rs573109859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27904169 | GCATAAATGACTTAG[A/G]AATTAACAATAGCTT | 55130 |
| rs573139029 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27818201 | CTTTCTGATCTTTAA[A/G]TTATTTCTTATATCA | 55130 |
| rs573155126 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27916751 | TATAACAACAAAATA[A/T]GTGCTAATTGTTTAT | 55130 |
| rs573156962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27824455 | ACTTGCTTCCACCTA[C/T]TGCCCTTCTGCCATG | 55130 |
| rs573191035 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27955763 | CAGTTTACATAAGAT[C/T]ATTAAGGAACTGAGC | 55130 |
| rs573212238 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27950645 | GGGCTGGAGTGCAAC[G/T]GTGTGATCTCGGCTC | 55130 |
| rs573252113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27837101 | TCATATTCATCCTGA[A/G]GGAAAATTTGTTGTC | 55130 |
| rs573310701 | snp | A/G | 0.00034082 | 0.0130497 | intron-variant | ARMC4 | GRCh38.p7 | 10:27985234 | AAAAAAAAAAAAGGA[A/G]ACAAATAAAAATTAT | 55130 |
| rs573318355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27916122 | GGGAATATCCCCACT[A/G]AGAATTAGCCTGGTA | 55130 |
| rs573334076 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27821467 | CAGGAATATGTTTTC[A/G]TTTTCCTACGAGCCT | 55130 |
| rs573355391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27892779 | ATCCTGTAATTCATT[A/G]CTGAAGTCTTTGATT | 55130 |
| rs573370401 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27895108 | AATTACAGGTGATTT[C/T]TTTAATTTGCTTTTC | 55130 |
| rs573371881 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27830706 | CCTGGAGCACTGGAG[G/T]GGATTGTATCTCTAA | 55130 |
| rs573385319 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27883303 | AGCTGAGTAGAAACC[G/T]CTGGAGTCATGCATG | 55130 |
| rs573400750 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27987784 | AAGAATTTTTTTTTT[G/T]TTTAGCAATTTCTTG | 55130 |
| rs573410010 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27930566 | CGGGAGGCGGAGTTT[G/T]CAGTGAGCCGAGATC | 55130 |
| rs573413375 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27929213 | AATTATTCTGGATAT[C/T]TCTGTATGTCTTTAG | 55130 |
| rs573440027 | snp | C/T | | | downstream-variant-500B, intron-variant | ARMC4 | GRCh38.p7 | 10:27812056 | ATCTCCTTGGAACTC[C/T]CCCGTGGGTTGCAAG | 55130 |
| rs573461150 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27991475 | GTTTCAGTATCAGAT[G/T]CTCATTAGCCTAATC | 55130 |
| rs573461898 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27987326 | CTCCCACCCTTTCCC[A/C]ACTTTCCCAGCAAGA | 55130 |
| rs573497265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984414 | GCAGTTAATTTTAGC[C/T]GTGCTATAATTTTAT | 55130 |
| rs573499714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27856177 | CAAATTTGTAATGAT[A/G]CAAATCCCTGGGCTG | 55130 |
| rs573505040 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27843706 | CTGGGAGGCACAGAT[A/G]CAATGAGCCGAGATC | 55130 |
| rs573521981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27980064 | AACAAGAATGCTGAG[A/G]CCATCCAAAAGAGAA | 55130 |
| rs573529289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27972897 | AGCAACACAATCAGA[C/T]AACTTGGCTTAATTG | 55130 |
| rs573548047 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27878550 | AAATTTTTAACCAGA[A/G]GAGCTATAAAAACAC | 55130 |
| rs573576675 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27925285 | AAATCATGATGAAAC[A/T]TATAGAGCACAGTCC | 55130 |
| rs573587557 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27925873 | AAATCAATTTAAAGA[A/C]TAAGAATTTTAAAGG | 55130 |
| rs573589345 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27822218 | TGCATTCAATTTTTA[A/C]ATTTCCATTTAACAG | 55130 |
| rs573622223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27994505 | AAGGCTGAGGCAGGA[A/G]GATCACTTGAGGCCA | 55130 |
| rs573645098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27857814 | ATGAATAGGCGACAC[A/G]GTGACTCTGGTCATT | 55130 |
| rs573647156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27865365 | TAGTCCTTCAGTTTT[C/T]ATGTCCTCAAATGTG | 55130 |
| rs573683688 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27864690 | GTGGGCCAAGGAAAA[G/T]AATTTGTCAGAAGAT | 55130 |
| rs573687085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27965793 | ATTTACAAAAATTGA[A/G]TTAGTGGAATCATGA | 55130 |
| rs573689393 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27979922 | CAGTACTAAAAAACA[A/C]AAACAAAGTTGGAGG | 55130 |
| rs573689509 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27845781 | GCAATCCTAGTCTCT[A/G]ATAAAACAGACTTTT | 55130 |
| rs573713149 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27972270 | AGGGCAGCTAAGAAA[C/T]TTTTAGTAAGAAATA | 55130 |
| rs573735934 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27932395 | ATTTTTGCACCATCA[A/C]ATATTAAAAATTTCT | 55130 |
| rs573738336 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27945179 | GCAGGCTGTCTCCTT[C/T]AAACAGCTTTAACAT | 55130 |
| rs573755545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27870752 | CTTAATCCACTCTAT[C/T]ATTGATGGACATTTG | 55130 |
| rs573769295 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27998423 | GGAAGGGACGGCGAA[A/C]ACCACGCTGGGAGCG | 55130 |
| rs573769649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27838613 | CTAAAGCTAGATAAA[C/T]ACAGAAACGAAATAT | 55130 |
| rs573787744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27963766 | TTATCATATAATATA[C/T]ATTGTATGAATTTCA | 55130 |
| rs573840177 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:28000064 | TCAAGAGATCCTCCC[C/G]CCTCAGCTTCCTGAG | 55130 |
| rs573850727 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27837188 | CAAGGATGCTCCCAC[C/T]CCTGTCTGTGCTGCC | 55130 |
| rs573864507 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27904570 | ACTAAATTCCCATTT[A/G]TACTTAGGTCTATTC | 55130 |
| rs573872199 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27905290 | GGTGAAAAAAAATAC[C/T]TAGGAATACAACTTA | 55130 |
| rs573894256 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | ARMC4 | GRCh38.p7 | 10:27952132 | CTGCAATTAGTATAA[A/C]AGCTAAAGGATTAAT | 55130 |
| rs573909039 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | ARMC4 | GRCh38.p7 | 10:27811921 | CAGTGACAGTTATAC[A/G]TTGTCCTTTCAGATG | 55130 |
| rs573933887 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27854103 | CCCGAGGAGTTATAC[A/G]GCTGATATACAAGCA | 55130 |
| rs573955350 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27937344 | TTTCTTTTTTCTTTT[A/T]TTTTTTTTTTTGAGA | 55130 |
| rs573966924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27911067 | GGCGTTTAGGGAATA[C/T]ACAGATTTTTTTCCA | 55130 |
| rs573973802 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27910061 | TATTTTAGCACCCAA[A/G]TCCCAGTCTTTACCA | 55130 |
| rs573975924 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27935400 | CTGAAGCTTGGTAAA[C/T]AGTAGAGCTGACGTC | 55130 |
| rs573984153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27951487 | GAAGGTGGTATCCCA[A/G]ATTATTGGAGGGAAA | 55130 |
| rs573988263 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27932349 | AGAATGGTTGTAGAG[A/G]TACTTGAAGTATAGT | 55130 |
| rs573991378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27844710 | AATGTGCTTTTAGAA[C/T]AAATGTCTGGCACAC | 55130 |
| rs574009041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27877158 | GTGTCTGATGGAATA[C/T]AAATTGATGAGATCA | 55130 |
| rs574023308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27924288 | ATTCTATTAAGCAAC[C/T]GGGCTAACAGGGGAA | 55130 |
| rs574027568 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999582 | CCTTTACCTTTGTCC[A/G]TTAAGATGGTTTTGA | 55130 |
| rs574030020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27844197 | AAGACCCTGTCTCAA[A/G]CCAAAAAAAAGAATA | 55130 |
| rs574036695 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27907408 | CTCTGATTTACCTGG[A/G]ATGCTTGCTTCCATT | 55130 |
| rs574041568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27971405 | AAATTCAGGAAAGGA[A/G]GTCTCGGATGCATTT | 55130 |
| rs574043562 | snp | C/T | | | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27857839 | GTCATTGTTAAAGAG[C/T]CTGTCAACATTCACT | 55130 |
| rs574060242 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27823866 | ATAGTTCAGGCCGGG[C/T]GCGGTGGCTCACGCC | 55130 |
| rs574065660 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27873942 | CGTTGATCCGTCTAA[A/T]GTTGACAGTGGGGTG | 55130 |
| rs574079679 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27943451 | ATCCTGTCATGATTT[G/T]ATACAATATTAAATA | 55130 |
| rs574095418 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27831284 | ACATTTATAAAATAT[G/T]AAATCTGTACATTTT | 55130 |
| rs574116743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944064 | TCACTAATATAAATA[C/T]GCAAAAATAATTCTT | 55130 |
| rs574125996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27910535 | CCAAGGTGGGTGGAT[C/T]GCATGAGCTCAAGAG | 55130 |
| rs574131089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27970701 | AGACGCAGTGACTCA[C/T]GCCTGTAATCCCAGC | 55130 |
| rs574166069 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983190 | CAGGCTCACCTCACC[C/T]CCTGGGAAATATCAC | 55130 |
| rs574173621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27876608 | ATAGCAGCCAATTAT[C/T]TGCTTAGGGCCCAAT | 55130 |
| rs574175899 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27931232 | TTAAAAGTCAGCATA[A/T]TACATATGGGTCAAT | 55130 |
| rs574178967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27909140 | CTAACGCCAATCTCT[A/G]AGCCTCTATTTTTTT | 55130 |
| rs574198962 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27822968 | CAGGAGACTCGCACA[A/C/T]TGGGTCTATAGTATT | 55130 |
| rs574213000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27923709 | TCTCAGTGCTTTGAG[A/G]AGCCAATGGGGGATA | 55130 |
| rs574231459 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27879434 | TTATATAGGAATATA[C/T]GTATATATTAAATAA | 55130 |
| rs574245683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27899153 | AGTGGGTACAGCCCA[C/T]GGAGGGCAAGCAGAA | 55130 |
| rs574290447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27977779 | TGTGAATGGCCAATA[A/G]GCACATGAAAAGATG | 55130 |
| rs574308063 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27903999 | TATGTTTTCTCCAAA[A/T]AAGGACTACCTGTTG | 55130 |
| rs574322461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27856920 | TGCAGTGAGCCGAGA[C/T]TGAGCTATTGCACTC | 55130 |
| rs574328875 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27950380 | TCTGTTTATTTGCAA[A/T]TCTATTTTACACTGA | 55130 |
| rs574364473 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27985406 | TTTCTTCTACTTCAC[A/G]AGATGCTCTAGTTTG | 55130 |
| rs574385051 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27856222 | GAAGTCTGTGCAAAA[C/T]CATAAAGAGAATAGG | 55130 |
| rs574400371 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27914706 | TATATATATGTGTGT[A/G]TATATAAATATGCAT | 55130 |
| rs574442437 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | ARMC4 | GRCh38.p7 | 10:27891928 | ACTTTCTGCAGCAGA[C/G]AGTTTTGCTTCTTAA | 55130 |
| rs574449198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27998702 | GGGAGCAGGCGAGAG[C/T]GGCAGCGGCGGGGCC | 55130 |
| rs574483398 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27845668 | TAGTGTGCTGTATTC[A/G]GGAGACCCATCTCAT | 55130 |
| rs574495762 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27903555 | TTTAGAAAACCCATC[A/G]TCTCAGCCGAAAATC | 55130 |
| rs574512687 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27955890 | GAGCTCTGGGAGTCC[A/C]TTCTGAAGCTGGCAG | 55130 |
| rs574516364 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27949786 | TGGATGCAGTCAGGT[C/T]ACTGCAGGGATCCAG | 55130 |
| rs574523864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27992188 | ATCAGCGCCAGGCAA[A/G]CATGGTTTCCTTCAA | 55130 |
| rs574570837 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27990655 | TGCAATAATTATTGT[C/G]TCATAAAACAATATT | 55130 |
| rs574575232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27923422 | CAGCACTTGAAATAT[C/T]AAAAGTCATAATTCA | 55130 |
| rs574579673 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27956474 | GAGTATGGGCAGATA[A/T]CCAACTGTGCTTGCC | 55130 |
| rs574592259 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27908691 | GCTTAAAATGCCATT[C/G]AAATTCTTCCTTGAA | 55130 |
| rs574634455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27863180 | ATTATAGCTCATGCA[A/G]TGGAGCTTATTTAAC | 55130 |
| rs574647983 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27996905 | TAGTGGTACTTGAGC[A/G]TTTACATGCCAATCT | 55130 |
| rs574652779 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27962979 | AATAATACCAACAGC[A/G]GCCACCAGTTTTGTC | 55130 |
| rs574655489 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27829988 | CCCCCAGACAAAACT[A/T]AATTCTTCTATGAAA | 55130 |
| rs574658866 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27840575 | TTCCCTTGTCTGAGA[-/T]TTTTTGAACTGAAAA | 55130 |
| rs574666992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27869876 | TAAGACATTATCATT[A/G]GACTTTCCAACAGTG | 55130 |
| rs574671143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27862356 | CCAGGTTTCTGGACT[A/G]CAAATGCATTGTTTT | 55130 |
| rs574694559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27835812 | CACTGGTAACCCCAG[C/T]TACCTCGGGAGGCTG | 55130 |
| rs574696262 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27835175 | CAAATCCTGCCACAG[A/G]CACAGGACCCATCTA | 55130 |
| rs574705402 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27975113 | TATCCTGAAACGTTG[C/T]TGAAGTTGTTTACCA | 55130 |
| rs574729494 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27989889 | AAAAATAAAAAACGC[A/C]AGCTATGGACAAGAT | 55130 |
| rs574740620 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27928866 | ATAAATTCACTTAAT[C/T]ATCTCAACAACCCAA | 55130 |
| rs574754552 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27996481 | TCGGCCTTTAGTGTT[C/G]AGGACCGACAATGTA | 55130 |
| rs574771410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27881547 | GAGGCTGAGGTGAGA[A/G]GATCACTTGAGCCCA | 55130 |
| rs574776573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27969315 | CTCTAGGTATGTATC[A/G]CCGCCAATTATAGTT | 55130 |
| rs574807908 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27839870 | AGTATAATAGTACAC[C/T]TCCTATAATCACAAA | 55130 |
| rs574837839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27868579 | AGCGAACTAACACAC[A/G]AACAGAAAACCAAAC | 55130 |
| rs574840616 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27843387 | GATGGTGTAGTGTAC[C/T]ACCCAGCATAACTGG | 55130 |
| rs574851325 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27975324 | AGCACCAAAGTAAAG[C/T]ATAAAAGATAAAAAT | 55130 |
| rs574889297 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983705 | GGATTTGCCCAGCAA[A/G]CATATATCAAAGGAA | 55130 |
| rs574925379 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27947517 | CATACTTAATTAAAG[A/G]AAATTAAATCATGCA | 55130 |
| rs574925812 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27931316 | CATTCCCCTGTTTGG[G/T]TGAATATAATTTTTT | 55130 |
| rs574931891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27902467 | CAGAACTGAAGGTGA[C/T]AGAGACAGGAAAAAC | 55130 |
| rs574945998 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27834335 | AGCTGCTCCAAAGGC[A/G]CTATCCCTTGGCCTT | 55130 |
| rs574947237 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27942464 | AAAACTGGTTTTGTT[A/C]CATGTTGTTTTGCTT | 55130 |
| rs574954080 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27948099 | GGTAAGAGTTTATAG[C/T]TTTTTGAAGTATCTC | 55130 |
| rs574964693 | in-del | -/T | 0.0163011 | 0.0887965 | intron-variant | ARMC4 | GRCh38.p7 | 10:27952861 | AAGGAGCTATGAAAC[-/T]TTTTTTTACATAAAC | 55130 |
| rs574978958 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27842391 | GAATGTCATTTTCTG[A/C/G]ATAGACACTAAGCAT | 55130 |
| rs574981728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27904053 | CAATCTGAGGTTTGG[A/G]GTTTTAAAAAACTCT | 55130 |
| rs575009523 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27861593 | CATTGATATCAGTAA[C/T]ACACCTTGGTTGCCT | 55130 |
| rs575012367 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARMC4 | GRCh38.p7 | 10:27907247 | ACCTTTTCAAAGCAA[C/T]ACAGAACGTAGTGCT | 55130 |
| rs575017512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27904483 | TCCATCTCAATAAAT[A/G]AAAAATATAAATAAA | 55130 |
| rs575024728 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27836633 | GGCAGCTTTAGGGCC[C/T]ATGAGCTTGCAGGGT | 55130 |
| rs575029675 | in-del | -/TTG | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997275 | CTCTTGAATTTCCCA[-/TTG]TTGTGTAAAATAAGT | 55130 |
| rs575034226 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27978135 | GGTGAGTGGATAAAC[A/C]AATTGTGGCATATCC | 55130 |
| rs575075615 | snp | A/C | 0.000132079 | 0.00812538 | missense | ARMC4 | GRCh38.p7 | 10:27860823 | AATAGCTTCTGCTAG[A/C]TGATGTCTCAATTTA | 55130 |
| rs575084743 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27898870 | ATAACAAATGATTCC[A/G]TTAATGGGTTTATAA | 55130 |
| rs575090308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27899543 | CCACTCCCACGGAGC[C/T]CAGCAAGCTAAGATC | 55130 |
| rs575118066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27955071 | CAACCCACATCAATG[C/T]AGCAACACATCTACT | 55130 |
| rs575121056 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27922860 | GCAGTGAGCCAACAT[C/T]GCACCACTGCACTCC | 55130 |
| rs575133630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27814557 | ATTTTTCATCACTTT[C/T]AACAGTCTGACCTCC | 55130 |
| rs575140872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27844785 | AGCTCTTTTACTATA[C/T]TTAGCTTTTCTTTTT | 55130 |
| rs575145143 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27903619 | CAGGATACAAAATCA[A/G]TGTGCAAAAGTCATA | 55130 |
| rs575145917 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27900286 | CATCAACAAAAAGGA[C/T]GTCCACAAAAAATCC | 55130 |
| rs575162671 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27938176 | ACTCCTGACCTCAGG[A/T]TATCCACACACCTCG | 55130 |
| rs575167475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27937420 | TCGACTCACTGCAAC[C/T]TCCACCTCCTGGGTT | 55130 |
| rs575183576 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27909218 | CTTCTTGAAAATTTC[G/T]CAGCAAATTTGGCAT | 55130 |
| rs575196249 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27826668 | AGGCTCATCTCCTTG[C/T]CCTCATGCTCTGCAT | 55130 |
| rs575226937 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27875815 | GGGAAGCTGTGAGAG[A/T]TGGCACCTGGAAAAT | 55130 |
| rs575231763 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27820492 | CTATTCCCGGAGTCA[A/C]CCAGATAAGGGTTGC | 55130 |
| rs575234560 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27892920 | TTGGGAGGCCGAGGC[A/G]AGCAGATCACTTGTG | 55130 |
| rs575247800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27947791 | CATACCTTGTTTAAG[C/T]CAAGAGCCTCCTCCT | 55130 |
| rs575254437 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944107 | TACAGACAGAAGGCT[A/C]CTGGAACACGCTCTC | 55130 |
| rs575265132 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27883152 | CTGACCTTGAGGTTC[C/T]ATACAAGCAGAAGTG | 55130 |
| rs575265836 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27993151 | AACTCCTGATCTCTG[A/G]TGATCTGCCCACCTC | 55130 |
| rs575268317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27986436 | ATGTCTACCAATTGA[A/G]TTGAATTGAATGAAT | 55130 |
| rs575270280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27977865 | TGTCTGTAGTTAAAA[A/G]ACTGACCATATCAGT | 55130 |
| rs575280563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27992316 | GTTGTATAGTAAATA[C/T]GACAGAAGTATAAAA | 55130 |
| rs575298944 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27882229 | AAAGAAAGAAAGAAA[G/T]AAAGAAATATGAACT | 55130 |
| rs575313567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27857644 | ATTCAAACTGAACAC[A/G]TTAGAAACTGAACTC | 55130 |
| rs575328341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27976444 | ATACAAAAATCAAGT[A/G]TATATTTATACAATA | 55130 |
| rs575332519 | snp | A/G | 3.29679e-05 | 0.00405991 | missense, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984238 | CTTTTCCTGAGAAAC[A/G]TTTGAGCAGTTCTAT | 55130 |
| rs575366505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27870602 | GAGTGAGAATATGCG[A/G]TGTTTGGTTTTTTGT | 55130 |
| rs575371910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27977125 | GGAAAGGTAAAATTG[A/G]AAAATCTCTAGAAGA | 55130 |
| rs575382851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27849102 | AAAGACACATGCACA[C/T]GTATGTTTACTGCGT | 55130 |
| rs575435048 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27855315 | CATGAACTTCTTTCT[A/C/T]ACTTTACAGGAGAAA | 55130 |
| rs575436393 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27816474 | ATTATAGGACTGTGA[A/T]TCATTTGAACAGCCA | 55130 |
| rs575440738 | snp | C/G | 0.0023933 | 0.0345097 | utr-variant-5-prime, intron-variant | ARMC4 | GRCh38.p7 | 10:27998816 | ACCTGCAGCACCCTG[C/G]CCCCCGCAGTCGGCG | 55130 |
| rs575447995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27856955 | CTGGACGACAAGACC[A/G]AAACTCCGTCCCAAA | 55130 |
| rs575455852 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27963717 | AATGCTCATGTTTTT[G/T]ATTACAGGGTATTGG | 55130 |
| rs575456422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27998268 | ATCGAACTTTTAGAC[A/G]TGACATGAACAGGGC | 55130 |
| rs575494355 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27949869 | AAGAAACGTTTGAAA[G/T]GTTTTTATCAACTTG | 55130 |
| rs575516101 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27990060 | CTTTTAAACCAGAAT[C/T]GTGGAAGGGAGCTAA | 55130 |
| rs575530745 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27950493 | ATATCCTTAAATAAA[G/T]CAGACTCAGGTTGTT | 55130 |
| rs575570525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27854703 | AGAGGTTGCAGTGAG[C/T]CCAGATCGCGCCACT | 55130 |
| rs575575949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27875429 | GGAGGGGGAGAGGCA[C/T]TCTGATTTTTAGAAT | 55130 |
| rs575581544 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27995303 | TTAATCTTGGAAGAT[C/T]CTTTTAACATTATCT | 55130 |
| rs575585685 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27831113 | CAACGGCCCAGGAGA[C/T]AGTGCTCCCAGAAGT | 55130 |
| rs575587450 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27888433 | TGGTGATATTGAGCA[C/G]TTTTTCATATTCCTG | 55130 |
| rs575601777 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27963063 | CCCAGGCTGTAGTGC[A/C]GTGGTGCAATCTTGG | 55130 |
| rs575602870 | in-del | -/TT | 0.00716266 | 0.059414 | intron-variant | ARMC4 | GRCh38.p7 | 10:27910070 | ACCCAAATCCCAGTC[-/TT]TACCATTTCATATCA | 55130 |
| rs575611073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27861566 | TGACTGGATTTCTCC[A/G]CCCTAGGAATACATT | 55130 |
| rs575613448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27955113 | TGTTTCTCAGGAACA[C/T]GGTACTCATTTGCCT | 55130 |
| rs575622718 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27830663 | AGAGCATAATTTTTA[G/T]GTTATACTGACTCGT | 55130 |
| rs575628176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27922790 | GCATGCCTGTAATCC[C/T]AGCTACTATGGTGGC | 55130 |
| rs575645299 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27906971 | TACCTATGTAACAAA[A/C]CTGCACGTTCTGCAC | 55130 |
| rs575661167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27836329 | GACTTGGCAGCAGAA[C/T]TCAGGGCCAGAATCC | 55130 |
| rs575686334 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27969358 | ATCTTCCCCACCCAA[C/T]GTTGCAACAGGGCCT | 55130 |
| rs575700355 | in-del | -/TAAAA | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27936219 | GATAGATTTGAAAAT[-/TAAAA]TAAATCAAATGGTCA | 55130 |
| rs575749992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27848259 | ACAGAGCCCTCAGAA[A/G]TAATACTACACATCT | 55130 |
| rs575754678 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27897791 | TAAGACAAGAAGAGG[A/G]CTGGAGGCAGGGAGT | 55130 |
| rs575757079 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27848662 | TGCAATCTACCCATC[G/T]GACGAAGGGCTAATA | 55130 |
| rs575778496 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27961438 | CCCTGCACAAACTTA[G/T]ATAAAACAACAGGAA | 55130 |
| rs575782662 | snp | A/G | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27834452 | CATTGGTGATAACCT[A/G]ATCATCACACGGCCA | 55130 |
| rs575784531 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27859082 | AAGACTGCATACTTA[C/G]GTTGTGCAAGTCCCT | 55130 |
| rs575787485 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27942714 | TTAATGAAAATTTTC[G/T]AACAGAAAAGCTTTA | 55130 |
| rs575807572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27835852 | AATCACTTGAACCCG[A/G]GAGGCAGGGGTGGCA | 55130 |
| rs575837857 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27960841 | TCAAATACTTTTTCA[A/C]AAATACTTCTGGACG | 55130 |
| rs575839189 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27815354 | AAAAAGACACCACTT[G/T]GACCCCATTTTCTTC | 55130 |
| rs575847861 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27824238 | TAGGAGAACATCAAA[A/T]CCTGCTATGGATTGA | 55130 |
| rs575864710 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27928599 | GGTGAGAGTTTAATG[C/T]GAATTATTTGCCATT | 55130 |
| rs575869948 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27979698 | GAAAACTTCTAAACA[G/T]TGCTGAAAGCCATTA | 55130 |
| rs575871306 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27897193 | TTCTTTACTTCACTC[C/T]GTCATTGGTGGTCTC | 55130 |
| rs575893810 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27956330 | ACTCTGATCAAAATC[C/T]CAGGTACAGAAGCTG | 55130 |
| rs575914334 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27990750 | AAGCTAAGGTCCAGA[A/G]AGGTATAAATTGTGT | 55130 |
| rs575995499 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27908519 | GAAGAAGGCCAAACA[A/T]AACTTAATAACCTTT | 55130 |
| rs575998086 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27861019 | CTTTTTTAGATGGAG[C/T]CTCACTCTGTTGCCC | 55130 |
| rs576000947 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997325 | AGTGTGAAATAAGTG[A/C]AAATAGCTTTATCTT | 55130 |
| rs576002735 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27868673 | ATAACACACATTGGG[G/T]CCTGCTGGGGCACGG | 55130 |
| rs576005529 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27868205 | GAGTCTGTGGAGAAA[A/T]AGGAATACTTGTACA | 55130 |
| rs576027168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27821265 | TTTGAGTTTTGCCGC[C/T]AACTAACTGTATTGT | 55130 |
| rs576041740 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27874484 | GCATGTTTTTGCAGT[A/G]GCTGGTACCAGCTGT | 55130 |
| rs576048870 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27934014 | TAATTGAATCATGGG[G/T]GCAGGTCTTTCCCAT | 55130 |
| rs576061009 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27858500 | CCCCCAAGAAACCCA[A/G]GGATAATCTGGGAAA | 55130 |
| rs576071699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27828495 | GACTGAAGGTAACTA[C/T]AGGTAAGTTTGTAGG | 55130 |
| rs576126488 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | ARMC4 | GRCh38.p7 | 10:27967478 | GAGGACTCCCTTGCC[G/T]GACCCCCCAGGCATC | 55130 |
| rs576150744 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | ARMC4 | GRCh38.p7 | 10:27874039 | ATGAATCTGGGTGCT[C/T]CTGTATTGGGTGCAT | 55130 |
| rs576159629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27975108 | TTTTGTATCCTGAAA[C/T]GTTGCTGAAGTTGTT | 55130 |
| rs576179049 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27913574 | ATGGGAGAAAATATA[C/T]GCAAACTATGCATCT | 55130 |
| rs576189985 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27920548 | GATTCGGAAGATTAA[A/G]TGATTCACATAATTA | 55130 |
| rs576194334 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27968624 | TGTTCAGAGGCAAGA[A/C]ATCAGTTAAGAGCCC | 55130 |
| rs576205095 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27864756 | TGGGGGTGAGTGTAA[C/T]GTCCACCAATTACTT | 55130 |
| rs576269620 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27918005 | GCCATATCTTTAAAT[A/C]AATTGAATTTGTAAT | 55130 |
| rs576276883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27906115 | TTTTGCAATCTATCA[A/G]TCTGACAAAGGGCTG | 55130 |
| rs576290027 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27896464 | GGTAATAGATGGATG[A/G]TTGATTGAAAGATAG | 55130 |
| rs576295121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27881221 | CAATAGTTTACATAA[C/T]TAAAATAATCAATCT | 55130 |
| rs576327407 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27889029 | TAGGTCCAGAAACAG[A/T]CAAAGCAGCATTTAG | 55130 |
| rs576336268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27880450 | TATATTGGAATTACC[C/T]GGAGAGTTTTTAAAA | 55130 |
| rs576359505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27853864 | TTTCTCAGATATGCA[A/G]CCAAAAACACAATTC | 55130 |
| rs576371156 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27889212 | GAAGCTGTGTGCCTA[C/G]AGAGATCAAGTTGGA | 55130 |
| rs576403502 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27982224 | TAAATACATATAACT[G/T]CAGTTTGTTATATAT | 55130 |
| rs576404532 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27848664 | CAATCTACCCATCTG[A/G]CGAAGGGCTAATATC | 55130 |
| rs576405198 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27939598 | CCTACATTAGCCAGG[A/C]ATGGTGGTAAACACC | 55130 |
| rs576407259 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27908450 | TTCTGTTTATATATC[A/C]ATCAGTCCAGGAGCA | 55130 |
| rs576409394 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27888182 | GGTAGATACCCAGTA[C/G]TGGTATTGCCAGATC | 55130 |
| rs576443834 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27995690 | GATGACTGAAGAACA[G/T]GATTCTGGTAGCTCT | 55130 |
| rs576465622 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27989297 | GGGACTGCCCCTATC[A/T]CCAGCACTTCAGATA | 55130 |
| rs576465882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27981312 | AATGATACTACATTT[A/G]CAGTATTTTTATGTT | 55130 |
| rs576468198 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27833302 | TCAGCAATTTGAAAA[C/T]ATTAGCACCCGGCAA | 55130 |
| rs576505312 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27996230 | AGAAGAATGGTTATA[C/T]GGTTAAATATAGAAT | 55130 |
| rs576517268 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27913780 | AATCAAAACCACAAG[A/G]AGATACTATCTCACA | 55130 |
| rs576518638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27821907 | AACACACCTAAAGAC[C/T]TTAAATTTATTGGGA | 55130 |
| rs576553324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27829862 | TCAGAGCCCATCTTA[C/T]ATGATTTTTGCCAAC | 55130 |
| rs576560878 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27953015 | ACATATAATTGATAT[A/T]AAAAAATGCACATCT | 55130 |
| rs576580777 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27940817 | CAACCTATAATAATA[A/G]ATAAATCCAATGTTC | 55130 |
| rs576590686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27829221 | AAGTACAGGGCTGGA[A/G]AGAAGAGCACAATTT | 55130 |
| rs576597100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27819169 | TGCAAACCCAAGTCT[A/G]CAGTGTGTGGGAGGG | 55130 |
| rs576597631 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872953 | CTCCTCCTTGTACTT[C/T]TGGTAGCATTCGGCT | 55130 |
| rs576601401 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27911350 | CGTGTCCAGGAATGA[C/G]AGCGCAAGTGATGTG | 55130 |
| rs576613377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872585 | TGTTGAATTTTGTCA[A/G]AGGCCTTTCCTGCAT | 55130 |
| rs576637472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27826149 | TGGAGGACGCAGAAT[A/G]GGATCAAGAACATCA | 55130 |
| rs576657941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27860047 | GTCCATATGCTGTAC[A/G]TTTTCTTTCATCAAA | 55130 |
| rs576669312 | snp | C/T | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27921822 | TATGAAGCAAGGCAA[C/T]AGAGCAGTATTTTAT | 55130 |
| rs576676430 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27959844 | GTTATGCTAAAAATT[G/T]CAGAGGTTTTCTGTA | 55130 |
| rs576680808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27919690 | TAGGAGTGTAAAATC[A/G]TACAATCACTTTTGT | 55130 |
| rs576686656 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARMC4 | GRCh38.p7 | 10:27859360 | GTTGACACATTCAAA[C/T]ATATATTGAGTTTAA | 55130 |
| rs576723986 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27964454 | GAAATATGTGTTTTA[A/G]TTCTGTATTATCAGG | 55130 |
| rs576724113 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27874315 | TCTTTACCCACTTTG[C/T]CAGTCTGTGTCTTTT | 55130 |
| rs576750668 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27956436 | AGTACTCAGGAATAA[C/G]ACCGCCTGGATGAAG | 55130 |
| rs576789314 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27862266 | AAAATACGCTTTCAC[A/G]TATATTAGTCTCAGA | 55130 |
| rs576798977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27926917 | GTATCAAATAGACAT[C/T]ACTTGATACTTACAA | 55130 |
| rs576801656 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27898578 | GACTGATTAAGATTA[C/T]CCTTCAAGGATTTGT | 55130 |
| rs576805026 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27990836 | TGTCCCAACTCCTAC[C/G]AGAATATATTTTTAT | 55130 |
| rs576817594 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27815660 | CCATTCATTCTCATC[A/T]TCTCAATCTTCATCC | 55130 |
| rs576824179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27832978 | GAAAGCATCAGTGCA[A/G]TATGGCTTTTCCAAC | 55130 |
| rs576836808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27966251 | TAATGAGCCACCTGA[A/G]TGAAGTTTCCAGTAG | 55130 |
| rs576840294 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27990855 | ATATATTTTTATCTC[A/G]ATGCATATATATCAC | 55130 |
| rs576847726 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27914636 | TATCTCCTCTGTAGG[C/T]AAAGGAGAAATATAG | 55130 |
| rs576852725 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27959379 | CCACTGCCAGTTCTT[C/T]TTTTCTTTCCCCCAG | 55130 |
| rs576860806 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27903162 | ATGCAAATCAATAAA[C/T]GTAATCCATCACATA | 55130 |
| rs576884838 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27908554 | ACATGGCTTTGTTTC[A/G]GAAAGGTATATTAAA | 55130 |
| rs576893833 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27986132 | CTTAAGGCTGAGAAA[A/G]GGACTTCACTGGGGG | 55130 |
| rs576907267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27996970 | GCACACTATCAATAT[C/T]TAAAACTATATTAAA | 55130 |
| rs576915476 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27901926 | AACAAGGATATTCGG[G/T]ACTTGAACTCAGCTC | 55130 |
| rs576919200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27955762 | TCAGTTTACATAAGA[C/T]CATTAAGGAACTGAG | 55130 |
| rs576936140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27961504 | AACTTGGAAGCAGCA[C/T]ATACATCTTTGGGAA | 55130 |
| rs576949820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27902289 | GCGTACCAGAATCTA[C/T]GGGAAATAGCTAAAG | 55130 |
| rs576954326 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27868720 | AGGATAAATAACTAA[G/T]GCATGCAGGGCTTAA | 55130 |
| rs576977459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27962214 | ATGTCCTAAGCCTGC[A/G]CTTTTCAATAAGACT | 55130 |
| rs576989874 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27928856 | CTTTACTTACATAAA[C/T]TCACTTAATCATCTC | 55130 |
| rs577001916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27914137 | TACAAACCATGGAGT[A/G]CTACACAGCCATAAA | 55130 |
| rs577074683 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27873844 | TCTGTTGATTTGGGG[C/T]GGAGAGTTCTGTAGG | 55130 |
| rs577083748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27969276 | TGCCACTGTTGGTGT[A/G]AATCCTGCACCCGAT | 55130 |
| rs577098166 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27968870 | TTGCATGCTCAGTAG[A/C]CCACTGCGTGAGGGT | 55130 |
| rs577101822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27875320 | CTCCTTTAGCTTGGA[A/G]AAGTTTGATCTTCTG | 55130 |
| rs577132160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27906778 | ACAAAAAACCAAACA[C/T]CGCATGTTCTCATTC | 55130 |
| rs577138050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27874743 | TTAGTCTGATGGGCT[C/T]CCCTTTGTGTGTAAC | 55130 |
| rs577158201 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27934810 | TCCTCCCAATATGAC[A/C]AACTTAGCCCTCCAT | 55130 |
| rs577158728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27941928 | ATTCCAAGTTCCTGG[A/G]AGAGAGATCCAGTGG | 55130 |
| rs577168747 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27889818 | GAGATTGGTGATCTC[A/C]TGTTGATAATAATGG | 55130 |
| rs577201358 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27975197 | CATTATTCACAACTG[A/G/T]ATTCCTCAAAATTTC | 55130 |
| rs577214880 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B, intron-variant | ARMC4 | GRCh38.p7 | 10:27811918 | GTACAGTGACAGTTA[C/T]ACGTTGTCCTTTCAG | 55130 |
| rs577220585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27941378 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGTGGG | 55130 |
| rs577241251 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27896502 | GATAAGCAGGCCATG[C/T]GTTTGTTGCCTGGAT | 55130 |
| rs577244761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27976225 | TTCAATTTTTTACTG[A/G]TGATTCCAGCTAGTG | 55130 |
| rs577251362 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27926323 | TCTGTAAAGTAGCGG[A/G]ATATAGAATTATCAT | 55130 |
| rs577260179 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27975446 | GAATGAGAGAGGTAA[A/C]AATGACTACAAATTC | 55130 |
| rs577276506 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27813935 | TGAAATAACTCTTCA[A/G]TAAATGGCCCCAGAA | 55130 |
| rs577283469 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27878653 | ATACAAACTTTTTTT[A/C]ATCCTACACTAACAT | 55130 |
| rs577286070 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27825339 | CCTAGCGAAAACAAA[A/T]ATGCTCAGATTCAGA | 55130 |
| rs577314276 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27847591 | ATCAGGCAGGAGAAA[G/T]AAATAAAGGGTATTC | 55130 |
| rs577315757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27980859 | AAAATAGGAACTCAA[C/T]AGATACCTGTACACC | 55130 |
| rs577350996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27973691 | CAGTCTCCCACTGAT[A/G]GCCATTTAGGTTGAC | 55130 |
| rs577376135 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27980057 | GATTTTCAACAAGAA[A/T]GCTGAGACCATCCAA | 55130 |
| rs577385801 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27860179 | CACACTGGCTGGGCA[C/T]TGTGACTCACTCCTG | 55130 |
| rs577390757 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983409 | AGGTCTGGGTCCCAG[C/T]TTCATAGGGCACTGT | 55130 |
| rs577406579 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27996332 | TTCTGTACTGTATTA[A/C]ATCTTTGAACTATCT | 55130 |
| rs577410434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27813495 | ACAAATGAATTAGAA[C/T]ATTTAAAATCTAGCA | 55130 |
| rs577418774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27867603 | AAGAAAGTAGCAGTG[C/T]CATCCTAGTCCACAT | 55130 |
| rs577432840 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27982339 | GTCTTTCATTTTTTT[A/T]AAACTTAAAGGGATA | 55130 |
| rs577442924 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27912948 | CCAAAGAGGCTATGG[C/G]ACAACAAATTTGGAG | 55130 |
| rs577445720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27920339 | GAACACACATATACA[C/T]GTATGCGCTCTCACA | 55130 |
| rs577453060 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27819807 | GATCAGCACAATGCA[A/T]CTAGATTTAAGAGAC | 55130 |
| rs577454699 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27853917 | CACCAGCGTTAAAAA[A/C]TTCTGCTCTTCAAAA | 55130 |
| rs577472152 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27995780 | TATAATTTTTTTTCT[A/G]AAAATTGATACAGGA | 55130 |
| rs577536611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27947477 | CTCTAAAATAATAAT[A/G]ATAAAGGAGAATCTA | 55130 |
| rs577548802 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27837086 | CTGATGCAAGAAAGG[C/T]CATATTCATCCTGAG | 55130 |
| rs577554660 | snp | A/G/T | 0.0123036 | 0.0774623 | intron-variant | ARMC4 | GRCh38.p7 | 10:27859273 | TTTAAAAGATGCTTT[A/G/T]GCCAGATTTTTGCTT | 55130 |
| rs577554824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27851052 | AATATTCGGCTCAGT[A/G]CTGCTTAGCACCTGT | 55130 |
| rs577576388 | in-del | -/C | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27998201 | CACGGGGAGTCCGCG[-/C]CATACACTGCTTTCT | 55130 |
| rs577581589 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27979008 | TGAGGCCAAGAGTTC[A/G]AGACCAGCCTAGTCA | 55130 |
| rs577597152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27828126 | ATGAAAACAGTCCCT[C/T]GGATTCTGACATTTG | 55130 |
| rs577611917 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27879309 | TAACCAATGATGTAT[C/T]TGGAAGAACTTTATA | 55130 |
| rs577631051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27887944 | ATAACCTAGATGAAA[C/T]AGACAAATTTCTAGA | 55130 |
| rs577668257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27895716 | ACCTTTTCATCATCA[C/T]GCAAAGTGCTATTAA | 55130 |
| rs577672518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27833715 | GGCACTGAACTAGTT[C/T]CTGGAAATGCAGGAG | 55130 |
| rs577694304 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27847110 | CCAAAGCCTGGCAGA[G/T]ACACAGAAAAAAAAG | 55130 |
| rs577702242 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27965886 | AAGTTTCTAACTCAA[A/C]ATTAAACTCACGGGC | 55130 |
| rs577723731 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27988527 | TTTTTAGTAGACAAC[A/G]GGGTTACACTATGTT | 55130 |
| rs577729041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27846402 | CACAACATACCAGAA[C/T]CTCTGGGACACATTT | 55130 |
| rs577738924 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27832338 | GACTTGATTTTATCA[C/T]GCATGCCCTCTTTCA | 55130 |
| rs577753361 | in-del | -/G | 0.0123036 | 0.0774623 | intron-variant | ARMC4 | GRCh38.p7 | 10:27868896 | GTAAACATAAAAAAA[-/G]AGAATAAGGAGCAAA | 55130 |
| rs577764150 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27958358 | TTATCCAGTAATTAG[A/G]CTATTATGAGAAACT | 55130 |
| rs577772314 | in-del | -/AAC | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27980656 | CGATGTTTATAATTA[-/AAC]AACAACCTAGAAAAT | 55130 |
| rs577778296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27831744 | GAGGCATAGCTGGTC[C/T]TCTCTGGCCCTTTGG | 55130 |
| rs577792452 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27914297 | CTGGTGACCACCAGA[A/C/T]CTTTCCATTTTAAAG | 55130 |
| rs577795968 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27916822 | GCTAAGTTTTGGGGA[A/G]GCCAAAAGTTATACA | 55130 |
| rs577796040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940449 | CTCTTTCTCATAGAA[C/T]GCTGACTTCTAGAAA | 55130 |
| rs577798924 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27895136 | TTCTTTAGTTTCTAA[A/G]ACTTATATAATGAAC | 55130 |
| rs577815035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27946119 | CATTATCTATTGTAT[A/G]ATTTTAAAATGTATT | 55130 |
| rs577822505 | snp | C/T | 0.0013181 | 0.0256381 | intron-variant | ARMC4 | GRCh38.p7 | 10:27939394 | CAATGGTTCTTAGAC[C/T]TGTCTATGAAAATCC | 55130 |
| rs577855772 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27941446 | GTTATGATCACACCA[C/T]TGCACTCCAGCCTGG | 55130 |
| rs577878821 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27987897 | ATTGGTTCTGCAAAA[C/T]CCTTCATGCTTTGGG | 55130 |
| rs577883034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27931782 | TGGCAATGACTTACA[C/T]AGAAATCATTAAAGC | 55130 |
| rs577895838 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27972020 | AAAATAAATATACAA[G/T]ACTTTGTGTATTATT | 55130 |
| rs577920742 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27924342 | CTAAAAATGATGATA[A/C]TGAAAGTACTATACA | 55130 |
| rs577920755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27932227 | AGATGTAAGCCACCA[C/T]GTCATTAGCCTATAG | 55130 |
| rs577933549 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27816997 | TCAGGTGATCCACCC[A/G]TCTCGGCCTCCAAAA | 55130 |
| rs577937416 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27823751 | TTTAATCTAGTTACA[C/T]TGAAAATTAATACAT | 55130 |
| rs577942789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27933235 | AGCCTGGGTGACAGC[C/T]TGAGTCCCTGTCTCT | 55130 |
| rs577967595 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27910499 | GGTGGCTCACGCCTG[C/T]AATCCTAACACTTTG | 55130 |
| rs577974609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27865635 | GGGTGAGGACTCTTG[C/T]TGTCTCATTCATTGT | 55130 |
| rs577988942 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27906004 | ATGGCAACAAAAGCC[A/C]GAATTGACAAATGGG | 55130 |
| rs577994775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27818572 | ATTAGAGGACCTAAT[C/T]CTATACTAAGAGCTT | 55130 |
| rs577997687 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27871947 | TAAATTACCTTGGGC[A/C]GTATGGCCATTTTCA | 55130 |
| rs578017643 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27918061 | CTTTTCATAAAAAAA[A/C]CTCCAACTTAGATAA | 55130 |
| rs578031373 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27883182 | GAAGTCTGAGAGTTG[A/T]AAACTGTAGTAATAT | 55130 |
| rs578031987 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27910671 | CTGAGGTAGGAGGAT[C/G]ACTTGAGCCCAGGAA | 55130 |
| rs578036117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27905491 | AAGCTACCACTGGCA[C/T]TCTTCACAGAATTAC | 55130 |
| rs578091507 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27972153 | CAAAGTATAGGGAGG[A/G]GTATTCAAGGTATAT | 55130 |
| rs578149326 | snp | A/G | 0.00398564 | 0.0444627 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:28000113 | TGCGCCGCCATGCCC[A/G]GCTAATTTTTGTACT | 55130 |
| rs578168191 | in-del | -/T | 0.0299202 | 0.118596 | intron-variant | ARMC4 | GRCh38.p7 | 10:27937946 | ATATATAGAGGTTTT[-/T]TTGTTTTTTGTTTTT | 55130 |
| rs578206410 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27845101 | AAGAGCAACTCCAAG[A/G]CACATAATTGTCAGA | 55130 |
| rs578223786 | in-del | -/TATTCTT | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27948423 | ATGTTAGCCAATTGC[-/TATTCTT]TAAATACCAGCTATG | 55130 |
| rs578241224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27884947 | TAGTGAAGGTCTTCC[A/G]AGCTGGTCTGCAAAA | 55130 |
| rs578248815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27978600 | GAGTTTGACACCAGC[C/T]TGGCCAACATGGGAA | 55130 |
| rs578259252 | in-del | -/CC | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27914296 | CTGGTGACCACCAGA[-/CC]CCTTTCCATTTTAAA | 55130 |
| rs587777047 | snp | A/C | | | missense | ARMC4 | GRCh38.p7 | 10:27862453 | TTTGCCAGTTTGGAC[A/C]ATAAAGGAACAACTC | 55130 |
| rs587777048 | in-del | -/G | | | frameshift-variant | ARMC4 | GRCh38.p7 | 10:27862521 | TGCTATGTTGGTAAT[-/G]GCAGCACATACACTT | 55130 |
| rs587777049 | snp | G/T | | | stop-gained | ARMC4 | GRCh38.p7 | 10:27862558 | ACTTCTTTGTTATCT[G/T]ATTTCAGTAAATTGA | 55130 |
| rs587777199 | snp | A/C | 3.29864e-05 | 0.00406105 | ARMC4 | 10 | allele_origin=A(germline)/C(germline) | 10:27940577 | CCTCTGATGCACACT[A/C]TTGCAATGTCCCCAC | 55130 |
| rs745321357 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27912347 | TCAGAAATCAAACTG[C/T]CTGGCTGGCAAAATA | 55130 |
| rs745322181 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27945099 | GAATCAGGTAGAGCC[A/G]AAGCATGGAAAAGCT | 55130 |
| rs745322546 | snp | C/T | 5.62003e-05 | 0.00530066 | intron-variant | ARMC4 | GRCh38.p7 | 10:27907615 | GGTGGCATTTTTCAG[C/T]ATAGTATTAGAGATT | 55130 |
| rs745359632 | in-del | -/A | 4.74507e-05 | 0.00487064 | intron-variant | ARMC4 | GRCh38.p7 | 10:27987559 | CTAAAAAATAAAAAT[-/A]AAAAATTGAAAGCTT | 55130 |
| rs745364784 | snp | A/G | | | missense, synonymous-codon, intron-variant | ARMC4 | GRCh38.p7 | 10:27812553 | CAAGAGCCAGCCTGC[A/G]GATATTGGATATACA | 55130 |
| rs745370054 | snp | A/G/T | 3.3283e-05 | 0.00407929 | intron-variant | ARMC4 | GRCh38.p7 | 10:27987371 | TCAAATCACAGACTG[A/G/T]AGCATTAAGATCACC | 55130 |
| rs745371936 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27958696 | GATTATTATTGCCAA[C/G]AGTTACTAACTACTT | 55130 |
| rs745382104 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27825234 | ATTACCATCACTGGT[C/G]TGAGCCACTACTATC | 55130 |
| rs745422042 | snp | A/G | | | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27958997 | TAAAGATAATGGACC[A/G]GGACTCTTGGGAAAA | 55130 |
| rs745437400 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27932857 | CAATGTTCCACACAT[A/G]TAATAGAATGTAATC | 55130 |
| rs745451850 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27872817 | TGGTCTAAAATTCTC[-/T]TTTTTTTTCTGTGTC | 55130 |
| rs745461070 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27985309 | TCAAAGTCCATTCAG[A/G]CGTGTTTCTTTCATT | 55130 |
| rs745483471 | snp | G/T | 1.65053e-05 | 0.0028727 | missense | ARMC4 | GRCh38.p7 | 10:27939974 | CAAGGTTTTCAATGA[G/T]CCTTTCTGCTTTGAT | 55130 |
| rs745490441 | in-del | -/AT | 1.69614e-05 | 0.00291211 | frameshift-variant, utr-variant-5-prime, intron-variant | ARMC4 | GRCh38.p7 | 10:27981476 | CTTACCAATTTAGAC[-/AT]ATTTTCTGAAAATTT | 55130 |
| rs745490492 | in-del | -/AGAA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27924049 | AAGAAAGAAGGAAAG[-/AGAA]AGAAAGAAAGAAAGA | 55130 |
| rs745510874 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27889003 | AGCTGAAGTTCTAAG[C/T]ATGTTGAGTTTAGGT | 55130 |
| rs745530568 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27896663 | CAGTACTCAGAGCAA[G/T]GTGTTTATAGGATTA | 55130 |
| rs745535759 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27986460 | AATGAATAATCCTTC[A/G]TCTATTAACTACCTC | 55130 |
| rs745554029 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27946948 | CTCAACAACTGTCCC[A/G]TGAAGATGTCACTGA | 55130 |
| rs745561773 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27900320 | TCTGAAGGTCACCAA[C/T]CTCAAAGACCAAAGG | 55130 |
| rs745562035 | snp | C/G | 3.75905e-05 | 0.00433518 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940059 | CGTGAATATAAGTAA[C/G]TGTTTACATTTATTA | 55130 |
| rs745581926 | snp | C/T | 1.65127e-05 | 0.00287334 | intron-variant | ARMC4 | GRCh38.p7 | 10:27860620 | ACAAAGTCATTCAAC[C/T]GTACCTTTACTGCAC | 55130 |
| rs745610618 | in-del | -/AA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27923995 | AAGAAAGAAAGAAAG[-/AA]AGAAAGAAAGAAAGA | 55130 |
| rs745673684 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27986643 | AATTCAAATACCTTG[C/T]GCCAGAAACCCATTG | 55130 |
| rs745691553 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27966461 | AAAAGCAGCGCCCCA[A/G]AGAAAAGCTGTCTTT | 55130 |
| rs745708685 | snp | C/G | | | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27857956 | ACAGCCAGGGTTTTG[C/G]CAAAATACTGGATAA | 55130 |
| rs745723561 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27870014 | ATATATATATAGTTG[C/G]AAGTATAAAATTTTA | 55130 |
| rs745737537 | in-del | -/TAT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27829614 | ATGAAACCTAAAACA[-/TAT]TATCGTAAAATTTCA | 55130 |
| rs745758676 | snp | A/T | 1.66263e-05 | 0.00288321 | utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27995146 | AGCCACACCCATGGG[A/T]TCCACCGTGCTCAGA | 55130 |
| rs745768522 | in-del | -/TATAT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27885732 | ATATTATATATAAAA[-/TATAT]TATATTATGTTATAT | 55130 |
| rs745771644 | in-del | -/A | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983708 | TTGCCCAGCAAGCAT[-/A]ATATCAAAGGAATCT | 55130 |
| rs745777302 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27895704 | TATCTGAACAATACC[A/T]TTTCATCATCACGCA | 55130 |
| rs745784537 | snp | C/T | 1.64827e-05 | 0.00287073 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27935105 | GAGGTTCACAAGTGG[C/T]TGAATGCCACCACAT | 55130 |
| rs745821792 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27879817 | CTGTAACTAATCTTA[A/G]TCTTTATGAATGCTC | 55130 |
| rs745824003 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27857452 | GGTCATGACCCCTAA[C/T]TCCTGCATTGTTCAA | 55130 |
| rs745825617 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27966043 | CCATTTTGGAGCATA[G/T]GAAGAGGATAGGCAA | 55130 |
| rs745856802 | in-del | -/TGTCTATGA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27939394 | AATGGTTCTTAGACC[-/TGTCTATGA]TGTCTATGAAAATCC | 55130 |
| rs745871418 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27954597 | TCGTTAAGTTGATGT[A/G]GTAGCATAGTGCTAG | 55130 |
| rs745897179 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27915880 | TGCCTACAATATGGA[C/T]ACAAACTGTTCACAT | 55130 |
| rs745907834 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27829621 | CTAAAACATATTATC[A/G]TAAAATTTCACAAAG | 55130 |
| rs745915403 | in-del | -/ATCA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27962844 | AGGAACTACTCATCC[-/ATCA]CTCACATGTGGAGAG | 55130 |
| rs745929683 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27815072 | CTCCTTCATAAACTC[A/G]ATCGAAGCCATTAGA | 55130 |
| rs745933373 | in-del | -/AGAT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27896474 | GGATGATTGATTGAA[-/AGAT]AGAGAGATAGATAAG | 55130 |
| rs745955758 | in-del | -/GTGTGTGTGTGT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27955699 | TTAACCAATTAAGGT[-/GTGTGTGTGTGT]GTGTGTGTGTGTGTG | 55130 |
| rs745985440 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27877941 | GCTTGAGGTTCATGT[A/T]TAGTTAGTGACAAAA | 55130 |
| rs746011673 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27865741 | CAAACTCATAGCCTT[A/G]AAAGAAAGCTTTCAC | 55130 |
| rs746023478 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27884580 | GTTTCTGTTTTATCT[A/G]ACTCAGAGCTCAGAC | 55130 |
| rs746027632 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27854088 | AATGTGAACACTTTG[A/C]CCGAGGAGTTATACA | 55130 |
| rs746054469 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27840024 | CATTAATAATTTACA[A/T]CGATTTAACTCACAA | 55130 |
| rs746083577 | snp | C/T | 1.73285e-05 | 0.00294346 | intron-variant | ARMC4 | GRCh38.p7 | 10:27860883 | GGGATCTGTGCATTG[C/T]AATGACCCTGCAAGA | 55130 |
| rs746104705 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27928225 | AAGTGGTACCAATAT[A/C]CATATAGTTACCCAA | 55130 |
| rs746122889 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27848698 | ATCTACAAAAAACTC[-/A]AAACATATTTACAAG | 55130 |
| rs746159645 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27964850 | CTTTTATACTGTCTC[C/T]CCTAGCACAAGGAAG | 55130 |
| rs746173842 | snp | A/G | 1.64895e-05 | 0.00287132 | missense | ARMC4 | GRCh38.p7 | 10:27860804 | CCCACATACAGCAAC[A/G]TGAAATAGCTTCTGC | 55130 |
| rs746175118 | snp | C/T | | | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27981843 | CCTCCTATATGCATG[C/T]AAGGCACTCTGCTGT | 55130 |
| rs746187558 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27925493 | CTCCTGAAAGGCTGG[A/T]ATTACAGGTGCACAC | 55130 |
| rs746202600 | snp | C/T | 0.000265278 | 0.0115139 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984312 | TAAATGTTTAAAATG[C/T]CAGCTTAAATACTTT | 55130 |
| rs746205825 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27938294 | ATTAAGGCTAAATGG[A/C]CTCTTCAAAATTACT | 55130 |
| rs746218140 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27836786 | AATAATTACTATCAA[A/T]TGATTGATTAATAAT | 55130 |
| rs746265664 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27990427 | GTGATCCTTCCATCT[C/G]CACCTTCCAAAGTGC | 55130 |
| rs746285604 | snp | A/G | 4.30191e-05 | 0.00463764 | missense, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27985050 | GAGAATGATTGAGGA[A/G]GTGCAGATCCAATTG | 55130 |
| rs746288840 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27892580 | GCTATCAATAACTAT[A/T]ACATACTTGCTTTCT | 55130 |
| rs746300769 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27891839 | AATAATCGTGTGATA[C/T]GACACAATTAAATTT | 55130 |
| rs746329994 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27825836 | AATGTTTCCTACACA[A/G]TAAGTGGAACAGTAG | 55130 |
| rs746344542 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27823096 | AATTGTGGGACATTG[C/T]TCAGCACCCTATATC | 55130 |
| rs746352431 | snp | A/G | 1.64833e-05 | 0.00287078 | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27936677 | AAATGACAAGAAGGT[A/G]TTTCAGAAGCCGTAT | 55130 |
| rs746359833 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27949189 | TTCATTCAACAAATG[C/T]GTTGCATGCTTCCTA | 55130 |
| rs746361822 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27928145 | TTGGAGGTATAATAA[C/T]GAACATATTGACTTT | 55130 |
| rs746365661 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27911290 | TTTTGGACCTCAGCA[C/G]AAAACATATGCACCA | 55130 |
| rs746366706 | in-del | -/CAGTATATGTGATATATATATAAATGC | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27940255 | TATATATATAAATGT[-/CAGTATATGTGATATATATATAAATGC]CAGTATATATGTGTG | 55130 |
| rs746373873 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27978929 | AAGATCAGGAGTCAG[A/G]CTAGGCATGGGGGCT | 55130 |
| rs746380952 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27893808 | AAGCTGGATGCCCCA[G/T]CATATTCAAAAAACA | 55130 |
| rs746392002 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27975075 | AATTCTGGTGATTTT[C/T]GTACGTTGATACATT | 55130 |
| rs746405520 | snp | C/T | 4.94401e-05 | 0.00497168 | missense, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27936786 | GTGACAGCAGCTAAC[C/T]GCTCTTTATTGTCAG | 55130 |
| rs746445850 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27985667 | CTTTCCAAAATAGCA[C/T]GCTTTCCTAAGCCTA | 55130 |
| rs746447265 | snp | C/T | 1.65337e-05 | 0.00287517 | utr-variant-3-prime, intron-variant | ARMC4 | GRCh38.p7 | 10:27812478 | ATGTCCTGTGTCATG[C/T]AGAATTTGATAGCTT | 55130 |
| rs746493497 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27869845 | TGGCCGACCAAGTCA[A/C]TTCTAAGGGAAAGAA | 55130 |
| rs746501231 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27813655 | AAAGAAATCTTACTA[A/C]GAAAAATATCGTGAG | 55130 |
| rs746534057 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27891530 | AACCCAACAACTGAC[C/T]TATTATACATTCAGA | 55130 |
| rs746549931 | in-del | -/AA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27924614 | AAATTGATTAGGAGG[-/AA]AAAAAAAAAAAAAAA | 55130 |
| rs746564548 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27850039 | CAAATGGACACAGCA[A/C]TAAAGTGAATATTAC | 55130 |
| rs746576267 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27889083 | ACAAAAGTGTTTCAG[A/G]CAAGGGTGCCAAATC | 55130 |
| rs746578210 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27901419 | ACTAATGGGCAAAAT[A/C]ACCAGCTAGCATCAA | 55130 |
| rs746581500 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27867923 | CACTGCACTCCAGCC[C/T]GGGTGACAGAGCAAA | 55130 |
| rs746585462 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27896075 | CAACATTTTGCTCAC[A/G]TATCCCAATGCACTT | 55130 |
| rs746605768 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27893728 | GGACAGGGGCAGTGA[C/T]GGGGAGAAAGAAAGG | 55130 |
| rs746609581 | snp | A/T | 1.85108e-05 | 0.00304221 | intron-variant | ARMC4 | GRCh38.p7 | 10:27907628 | AGTATAGTATTAGAG[A/T]TTCTAGAAGAGACTG | 55130 |
| rs746614686 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27917590 | AAAAGTAGGTTCTTT[C/T]AAAAGGTGAATAAAA | 55130 |
| rs746625018 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27818973 | GGGCACATCACTGAA[C/T]CTCTTAACCCAACCT | 55130 |
| rs746625384 | snp | A/T | 1.65105e-05 | 0.00287315 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27987480 | AATTTTAATTTGTGG[A/T]ACAGAGAGAAATAGC | 55130 |
| rs746652922 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27906880 | GGGTGCGGGACTAGG[A/G]GAGGAATAGCATTAG | 55130 |
| rs746685002 | in-del | -/AAAAAAAAAAAAAAA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27819575 | GAGACCCTGTCTCTT[-/AAAAAAAAAAAAAAA]AAAAAAAAAAAAGTT | 55130 |
| rs746690244 | snp | C/G | 3.30387e-05 | 0.00406427 | missense, intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27971258 | GCTTCTTCCTTCTTG[C/G]GGGCTTTGCCAAGCT | 55130 |
| rs746740821 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27908091 | GTAAAAATACGGGTT[A/T]CTTTCATATAGTAAC | 55130 |
| rs746767014 | snp | A/T | | | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27996245 | CGGTTAAATATAGAA[A/T]AAAATTGGCTTTTTA | 55130 |
| rs746772221 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27826541 | GAAAATAGAAATCAC[A/G]AAAAGGGAAGTGGCC | 55130 |
| rs746774246 | in-del | -/AA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27855133 | ATGTCAAAATCTATC[-/AA]AGTGTACACCTTAAA | 55130 |
| rs746792712 | in-del | -/GTGTGTGTGT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27955699 | TTAACCAATTAAGGT[-/GTGTGTGTGT]GTGTGTGTGTGTGTG | 55130 |
| rs746793265 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27972590 | TGGAGAAGAATAGTT[C/T]ATGCAAACAATAATC | 55130 |
| rs746829907 | snp | A/G | 4.94474e-05 | 0.00497205 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27940737 | GCGAGCCACTTCCAC[A/G]TCTCTGGCCTCATAC | 55130 |
| rs746832445 | in-del | -/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27873061 | TATTGAGGGATTCAA[-/C]CTTCTTCCTGGTTTA | 55130 |
| rs746836213 | snp | A/T | 3.34359e-05 | 0.00408862 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940519 | CTTTTGGACTAAAGA[A/T]AGTCAAGTTGAGAAG | 55130 |
| rs746892581 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27859139 | AATTAGAAATATCTT[C/T]CTTTTTGAAATGGGA | 55130 |
| rs746894085 | snp | A/G | 1.65244e-05 | 0.00287436 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984006 | CATCAAGCAATTAAC[A/G]GGAGTTCCTTAACCT | 55130 |
| rs746897925 | snp | G/T | 1.64792e-05 | 0.00287042 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27944867 | CAGCACTTCCAGGCC[G/T]CCAACATCTCTGATG | 55130 |
| rs746941462 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27898378 | AACAGTTTATGTGAA[C/T]CCTTAGGTGTTTCTG | 55130 |
| rs746942166 | snp | C/T | 1.64972e-05 | 0.00287199 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27860631 | CAACTGTACCTTTAC[C/T]GCACCATTCTCATGC | 55130 |
| rs746949257 | snp | A/G | 4.94645e-05 | 0.00497291 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944971 | TTCCTCCCTACAAAG[A/G]TGCAATGCCAGAGAA | 55130 |
| rs746979671 | in-del | -/TAAT | 0.0011804 | 0.0242654 | intron-variant | ARMC4 | GRCh38.p7 | 10:27969062 | TTTATTGCTTTATGC[-/TAAT]TAATAAAAAATAAAA | 55130 |
| rs746990495 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27942530 | GAATGAAGACTTACT[A/G]TACTAGGTTCCTGAA | 55130 |
| rs747025151 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27993575 | GAATTGCTTGAACCA[A/G]AGAGGTGGAACTTGC | 55130 |
| rs747033579 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27919701 | AATCGTACAATCACT[G/T]TTGTGTACTATTTGG | 55130 |
| rs747037206 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27951450 | GAAACAAACTCTCAC[A/G]TGTGAGACTGCAGAA | 55130 |
| rs747052558 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27903886 | AGACAAGGGTGTCCA[C/T]CAACCAGGGAGACCA | 55130 |
| rs747078043 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27817492 | TTTTTTAACCCTCAT[C/T]CCCCCTCCCCATTTC | 55130 |
| rs747096423 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27816486 | TGATTCATTTGAACA[A/G]CCATATGGTCTGTGC | 55130 |
| rs747117951 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27965075 | GCCAAGATTTGGTAC[C/T]GGTTTTCCTCTTGGG | 55130 |
| rs747118230 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27837150 | AAAGACACCAGCATC[C/T]CGGCTGCCTCTCTGG | 55130 |
| rs747129111 | snp | G/T | 1.65206e-05 | 0.00287403 | missense, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983902 | TCTCACCATCGTGAG[G/T]TTTCACCAGCACATA | 55130 |
| rs747132563 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27992588 | CTAGCTGCTTGAGGG[A/G]CTGAGGTGGGAGGAT | 55130 |
| rs747168408 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27863842 | TTTTCTAGTTCAGAA[C/T]GACTGGAGCACAAAA | 55130 |
| rs747171647 | in-del | -/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27915270 | AGAATGCCATATGCT[-/G]GGGTGGCTTGTAAAC | 55130 |
| rs747183308 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27868655 | ATAGATACAGGGAAG[A/G]GAATAACACACATTG | 55130 |
| rs747187493 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27926895 | TACCTCCAGATAAAT[G/T]TTATAAGTATCAAAT | 55130 |
| rs747193046 | in-del | -/GAAAGAAAGAAA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27923965 | AAAGAAAGAAAGAAA[-/GAAAGAAAGAAA]GAAAGAAAGAAAGAA | 55130 |
| rs747225248 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27924187 | AACACACTCTGATCA[A/G]AATGTAGTATGAGAA | 55130 |
| rs747226807 | snp | A/G | 5.32935e-05 | 0.00516178 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944205 | TAGATGACGATGACA[A/G]CATCACGGCTACTCA | 55130 |
| rs747234154 | snp | C/G | 1.71711e-05 | 0.00293006 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940852 | AAATCTTAAAAAGAA[C/G]ATTTAAGGCATTCTT | 55130 |
| rs747239488 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27948550 | TTAAATCTCCCCTAA[A/G]AACATAATTATTTAC | 55130 |
| rs747252160 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27855618 | AATCCGTTTACTTGA[C/T]TCACAAACATTAACA | 55130 |
| rs747260565 | snp | C/T | 1.64822e-05 | 0.00287068 | missense | ARMC4 | GRCh38.p7 | 10:27935124 | ATGCCACCACATTTC[C/T]GGACAATGACTCGGT | 55130 |
| rs747278355 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27952612 | TCCATGTGTTCTCAT[A/T]GTAGATGAACAGTTT | 55130 |
| rs747278455 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27938410 | AGGGAAAAGGCAGCC[A/G]TCTACAAGCTGAGGA | 55130 |
| rs747352518 | snp | A/T | | | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27958862 | TTGAGTAAGCGGCAG[A/T]ATTTCAACTCAACTG | 55130 |
| rs747365004 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27825413 | AAGAGAAAAGACAAC[G/T]TAGTGATCTGGGAGG | 55130 |
| rs747377242 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27861620 | GCCTTGGCTCCTGAG[A/G]GGGAGAAGAGAGTGC | 55130 |
| rs747390233 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27823330 | GAATTGCATTTTGCT[A/G]TTGGTTAGATCAAAG | 55130 |
| rs747394993 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27822432 | AAGTGCCCAGAGCTG[A/C]TTTGAACTGGGAACC | 55130 |
| rs747397097 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27977729 | ATGAAAAAAACAGAC[A/G]AAGAGTCCAAATAGA | 55130 |
| rs747418750 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27908083 | ACCTAAATGTAAAAA[C/T]ACGGGTTTCTTTCAT | 55130 |
| rs747430257 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27838747 | AAAAGGAGCAGCATA[C/T]ACTTTATTTTACCAT | 55130 |
| rs747433352 | snp | A/G | 2.16097e-05 | 0.003287 | missense, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27985055 | TGATTGAGGAGGTGC[A/G]GATCCAATTGCTTAA | 55130 |
| rs747439529 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27880452 | TATTGGAATTACCTG[A/G]AGAGTTTTTAAAACT | 55130 |
| rs747443395 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27971994 | AAAAATTAAAAGCTG[A/C]AGAAATGGTAAAAAT | 55130 |
| rs747464324 | snp | C/G | | | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:28000633 | CAGCCAGAGATCTTC[C/G]AAGTTCAGGACATTT | 55130 |
| rs747472547 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27864146 | GGTGATGGTTTGGGG[C/G]AGGGTGGTGGTCTAT | 55130 |
| rs747473192 | snp | A/G | 0.00110436 | 0.0234726 | intron-variant | ARMC4 | GRCh38.p7 | 10:27968897 | GGGTGGCTTTAGGGA[A/G]CTCGTCTTGCTGACC | 55130 |
| rs747488108 | snp | C/T | 1.67677e-05 | 0.00289544 | missense, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27961687 | AGGAGCTATCGCTAA[C/T]AGTTTCCTCAATCTT | 55130 |
| rs747499395 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27812922 | TTGCATCTTTTCTGT[C/T]TTTTCCACCTCTCAG | 55130 |
| rs747502734 | snp | C/T | 3.5049e-05 | 0.00418608 | intron-variant | ARMC4 | GRCh38.p7 | 10:27862401 | GATATCTCAGGACAA[C/T]ATGCATGTAAAACAA | 55130 |
| rs747517841 | snp | G/T | 1.65042e-05 | 0.0028726 | missense | ARMC4 | GRCh38.p7 | 10:27860818 | CGTGAAATAGCTTCT[G/T]CTAGATGATGTCTCA | 55130 |
| rs747525602 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27881455 | GGCAACATAGCAAGA[A/C]TTCTGCTTCTACAAA | 55130 |
| rs747546905 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27906451 | TGTGGAAGACAGTGT[A/G]GCGGTTCCTCAAGGA | 55130 |
| rs747572868 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27912602 | GTTTCTTTCTGGCAA[C/T]ATCAACATATCTATT | 55130 |
| rs747614472 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27979273 | AATCAGACAAGGATG[C/T]CTGCTTTTACCACTC | 55130 |
| rs747620256 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27945389 | GAACTCAGAGAAAAG[A/G]AAAACGTGCAGGAAG | 55130 |
| rs747627960 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27972876 | AGTAATGATATAGAA[G/T]ATATGAGCAACACAA | 55130 |
| rs747631889 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27835315 | TCAATGTACAGGAAC[A/G]GGACTTTAATTCAGG | 55130 |
| rs747675835 | in-del | -/AA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27924007 | AAGAAAGAAAGAAAG[-/AA]AGAAAGAAAGAAAGA | 55130 |
| rs747682443 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27988590 | GGATCCACACACCTC[A/G]ACCTCCCAAAGTACT | 55130 |
| rs747698616 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27914515 | TGTTACTTGACATTA[A/T]TCTATGAAAAAGAGC | 55130 |
| rs747707303 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27826109 | TCTCTGCCTCTCGTT[A/G]CTGTCTATCAGAAAT | 55130 |
| rs747716966 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27834333 | AAAGCTGCTCCAAAG[A/G]CGCTATCCCTTGGCC | 55130 |
| rs747722445 | snp | A/G | 0.000152912 | 0.00874257 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944460 | AAAAAGATGAGTGGC[A/G]AATATGTAACCCGTG | 55130 |
| rs747727153 | snp | A/C | 4.95274e-05 | 0.00497607 | utr-variant-3-prime, intron-variant | ARMC4 | GRCh38.p7 | 10:27812491 | TGTAGAATTTGATAG[A/C]TTGTAATGTCCATTT | 55130 |
| rs747751106 | snp | A/G | 1.77748e-05 | 0.00298112 | intron-variant | ARMC4 | GRCh38.p7 | 10:27981424 | AAGTTGTAGTTTAGT[A/G]ACATAATGCTATGAA | 55130 |
| rs747752366 | snp | C/T | 1.64798e-05 | 0.00287047 | synonymous-codon, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27936791 | AGCAGCTAACCGCTC[C/T]TTATTGTCAGTGTTA | 55130 |
| rs747755003 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27852626 | GTAAAGAGAAAAAGC[A/T]GATGGGAAAAATAGA | 55130 |
| rs747759687 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27938423 | CCGTCTACAAGCTGA[C/G]GAGAGAGGCCTCAGA | 55130 |
| rs747772379 | snp | A/T | 5.03571e-05 | 0.00501757 | intron-variant | ARMC4 | GRCh38.p7 | 10:27907816 | ATATAAACTGTCATT[A/T]GTATGTGAAGACAAA | 55130 |
| rs747784854 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27911094 | TCCAAAAGGAACATC[A/G]CCGCCGTCCTGCACT | 55130 |
| rs747798871 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27909314 | TGGCACAAATTTGCA[A/G]TTTAAAAAAAGGAAC | 55130 |
| rs747804167 | snp | C/T | 3.29826e-05 | 0.00406082 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27944374 | CCCCAAGGTCAACAA[C/T]ATTCTGTCTGATTTG | 55130 |
| rs747810276 | snp | C/T | 4.95364e-05 | 0.00497652 | intron-variant | ARMC4 | GRCh38.p7 | 10:27981605 | AAAAAACAAGTTTCA[C/T]TCTATGATTAACATA | 55130 |
| rs747821786 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27940145 | ATATCCCTACATCAA[C/T]AAGAGAATCAACTGA | 55130 |
| rs747861861 | snp | G/T | 1.64822e-05 | 0.00287068 | missense, synonymous-codon, intron-variant | ARMC4 | GRCh38.p7 | 10:27812565 | TGCGGATATTGGATA[G/T]ACAACCAGCTGCAGC | 55130 |
| rs747873854 | snp | A/C | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27982801 | TGTTGCAGAGGTGAA[A/C]GCTAAGCTCCTTCTA | 55130 |
| rs747895277 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27898702 | TTATATTATATATCT[A/T]TTTCTGCAAGTTTTT | 55130 |
| rs747907044 | in-del | -/CA | 0.000103631 | 0.00719754 | intron-variant | ARMC4 | GRCh38.p7 | 10:27945003 | GGTTAAGGAACACCG[-/CA]TTCCCATAGAAATGC | 55130 |
| rs747912550 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27877388 | GGAGCCAAAGTCCCC[A/G]TGAGATCATGGGCAC | 55130 |
| rs747916255 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27998438 | AACCACGCTGGGAGC[C/G]GGAGGCAGAGCTGCA | 55130 |
| rs747925714 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27828710 | ATATAAAGAAGCTTT[A/C]CATGAAATAATTTTG | 55130 |
| rs747934694 | in-del | -/AA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27970817 | AAAATTACAAAAAAT[-/AA]AAAGTTAGCCAGGCG | 55130 |
| rs747965765 | snp | A/C | 1.6797e-05 | 0.00289797 | stop-gained | ARMC4 | GRCh38.p7 | 10:27987521 | CATTTTTATCAACTT[A/C]TTCTGATTTGACTGT | 55130 |
| rs747966291 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997734 | AAAATAAATAAATAA[A/G]TAAATGGTGTTCAAA | 55130 |
| rs747978352 | snp | A/G | 1.65436e-05 | 0.00287602 | missense, intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27971271 | TGGGGGCTTTGCCAA[A/G]CTGATCCTTTTCCTT | 55130 |
| rs747995013 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27829905 | AGCTTCAGGACTGGC[C/T]CTAAGCAAGGTATTC | 55130 |
| rs748016173 | snp | C/G | 3.30196e-05 | 0.00406309 | missense | ARMC4 | GRCh38.p7 | 10:27907718 | CTGGCCTTCACGTCT[C/G]GGTGAGGATTTTTCA | 55130 |
| rs748039523 | in-del | -/AAAAAAAAAAAAA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27943797 | TGAGGCTCTGTCTCA[-/AAAAAAAAAAAAA]AAAAAAAAAAAAAAA | 55130 |
| rs748075641 | snp | C/T | 1.66613e-05 | 0.00288623 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940536 | GTCAAGTTGAGAAGG[C/T]AAGGGAAGCAGAACT | 55130 |
| rs748077762 | in-del | -/GCGCAGTGCT | 1.66322e-05 | 0.00288371 | frameshift-variant | ARMC4 | GRCh38.p7 | 10:27939913 | TGGTAAATGGCCATG[-/GCGCAGTGCT]CCTGCAGCTGCTCAT | 55130 |
| rs748090989 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27921833 | GCAATAGAGCAGTAT[-/T]TTATTTTTTTTTTTG | 55130 |
| rs748101941 | snp | A/G | 0.000148311 | 0.00861007 | missense | ARMC4 | GRCh38.p7 | 10:27940627 | TCATGAGAAGTCTTC[A/G]GCAGCCGAGCCAACA | 55130 |
| rs748149773 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27923541 | GAGAATTTCATACAG[A/C]AGTTACAGCATAAGA | 55130 |
| rs748168404 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27894423 | TCGTAAAATAAACTA[C/T]TATTTTATGTACCAC | 55130 |
| rs748170644 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27906281 | ATCATCACTGGTCAT[C/T]AGAGACATGCAAATC | 55130 |
| rs748172444 | snp | C/T | 1.64806e-05 | 0.00287054 | missense | ARMC4 | GRCh38.p7 | 10:27860707 | TGAGCTGTCGCCCGA[C/T]GCACGTTGGTGTCAT | 55130 |
| rs748222185 | in-del | -/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27921143 | AATCCTGGGCACTTA[-/C]AAAATATTAATAGAA | 55130 |
| rs748239210 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27838771 | TTACCATACTGTTTG[C/T]GTATTTTTGACCCTC | 55130 |
| rs748244504 | snp | A/C | 1.6498e-05 | 0.00287206 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944987 | TGCAATGCCAGAGAA[A/C]GGTTAAGGAACACCG | 55130 |
| rs748254755 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27887878 | AACTAAAATTAGAAA[C/T]AGAAAAGATTGTAAG | 55130 |
| rs748276257 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27952803 | AGGGTTGAAAACTAT[C/T]GGTATGTTACTGGTA | 55130 |
| rs748288183 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27948082 | GCAGCAGATGTCCCA[A/T]AGGTAAGAGTTTATA | 55130 |
| rs748290355 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27992936 | ATATTAATTTTTTTT[C/G]AGATGGAGTTTCTCT | 55130 |
| rs748298602 | snp | C/T | 4.948e-05 | 0.00497369 | missense, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984271 | CCTTCTTCACCGTCA[C/T]GGGACTTAAACTTAT | 55130 |
| rs748327180 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27857264 | ATTTTCTCTTCCTTA[C/T]GATTCTCATAACACT | 55130 |
| rs748332038 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27825496 | TAATACTGAACTCAG[A/T]AGTTGCTGGAATTGC | 55130 |
| rs748334350 | snp | A/G | 1.65666e-05 | 0.00287802 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984025 | GTTCCTTAACCTAGA[A/G]TTTGGTAAAAAGTGT | 55130 |
| rs748352808 | snp | C/T | 1.66618e-05 | 0.00288628 | intron-variant | ARMC4 | GRCh38.p7 | 10:27935280 | TAAGAAAGAGGAGAA[C/T]TGGTTTTTGTATAAG | 55130 |
| rs748367712 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27929291 | TGAATAGATGAGAGA[C/T]GATTGATAGATAAAA | 55130 |
| rs748381755 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27979677 | AAGGAGAAAAACTTG[C/T]ACACTGAAAACTTCT | 55130 |
| rs748401451 | snp | C/T | 1.64882e-05 | 0.00287121 | missense | ARMC4 | GRCh38.p7 | 10:27860642 | TTACTGCACCATTCT[C/T]ATGCATGGTGATGCA | 55130 |
| rs748455299 | in-del | -/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27846169 | ATTGACCACATAGTT[-/G]GAAGTAAAGCACTCC | 55130 |
| rs748466849 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27947266 | AGTACTTCCATTTCC[C/T]CTTTTAAAAAAACAA | 55130 |
| rs748466863 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27961417 | CCTCAGGGTAATAAG[A/G]CCTTGCCCTGCACAA | 55130 |
| rs748480458 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27914133 | TACATACAAACCATG[A/G]AGTACTACACAGCCA | 55130 |
| rs748520073 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27960432 | GCTCACTGCAACCTC[C/T]GCCTCCTGGGTTCAA | 55130 |
| rs748525292 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27940967 | CCACGGAAAGCAAAG[-/A]AACAAAACCCTACAA | 55130 |
| rs748530119 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27813050 | ATATCAGTCACTTAA[C/T]AGGGACTCTCAGTGC | 55130 |
| rs748556035 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27980987 | AAACAAAATATTATT[C/T]TACCATAAAAGAATG | 55130 |
| rs748558108 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27844867 | GCGATGGGGTGGTGG[C/T]GAAGGAGTTGGATTT | 55130 |
| rs748561638 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27842658 | ACTAAAAGTAGAAGC[C/T]AAAAATAATTCCCCA | 55130 |
| rs748565110 | snp | C/G | 1.67013e-05 | 0.0028897 | utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27995155 | CATGGGATCCACCGT[C/G]CTCAGACCTGAGCTT | 55130 |
| rs748573688 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27902226 | GTAAATAACGAAATT[A/C]AGGCAGAAATAAATA | 55130 |
| rs748577492 | snp | A/T | 1.65209e-05 | 0.00287405 | stop-gained | ARMC4 | GRCh38.p7 | 10:27862562 | CTTTGTTATCTGATT[A/T]CAGTAAATTGACAAT | 55130 |
| rs748592032 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27936077 | CTACGCCTTATTAAG[C/T]AAACTTATTTTGTGT | 55130 |
| rs748598759 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27986990 | TTGTCATTCAATCTA[C/T]TCCTTGGCAGTATGC | 55130 |
| rs748608265 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27956539 | GGACAATACGGGCAT[C/T]TTATCCTGTAGTGAC | 55130 |
| rs748615388 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27883071 | AATCTAAAAGGCTAC[A/G]TACATGTGTCAGGTT | 55130 |
| rs748623134 | snp | C/T | 3.38129e-05 | 0.00411161 | intron-variant | ARMC4 | GRCh38.p7 | 10:27987343 | CTTTCCCAGCAAGAT[C/T]GTTTCTAAAAGTTCA | 55130 |
| rs748678319 | snp | C/T | 1.65389e-05 | 0.00287562 | intron-variant | ARMC4 | GRCh38.p7 | 10:27971099 | AAACAAATGCAAATA[C/T]CTACATACCCTTTGT | 55130 |
| rs748684677 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27850173 | ACATTTGCTGGGCGT[A/G]GCGGCTCACACCTGT | 55130 |
| rs748687262 | in-del | -/GAA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27968043 | CAATATCAAGGTGAT[-/GAA]GAAGTATGAATTATC | 55130 |
| rs748703417 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27865278 | TGATTCATTAAGTCT[C/G]GGTGAGGTCCACTAA | 55130 |
| rs748711643 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27901510 | CCCAATTAAAAGACA[C/T]AGATTGGCAAATTGG | 55130 |
| rs748726615 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27926235 | TAAAAGTAAGATTTG[G/T]CCCATAAACCATAGT | 55130 |
| rs748782405 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27957560 | TCATTGCTTCCTTTA[G/T]AATTAGGGTACAGCA | 55130 |
| rs748814791 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27878321 | AATACATTTGGTTAA[A/G]ATTCAACTAATGGGA | 55130 |
| rs748825397 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27821839 | GGGGCTTACCTTTTT[G/T]AAGTCCTTGTTCCTT | 55130 |
| rs748836506 | in-del | -/TTT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27988338 | AACACCTGATCTAGC[-/TTT]TTTTTTTTTTTTTTT | 55130 |
| rs748854227 | snp | A/T | 3.38083e-05 | 0.00411133 | missense | ARMC4 | GRCh38.p7 | 10:27985159 | TGCAATTGAGTTTTC[A/T]TTCATTGTATTATAA | 55130 |
| rs748857448 | snp | C/T | 3.30028e-05 | 0.00406205 | missense | ARMC4 | GRCh38.p7 | 10:27939955 | TCACTATTTAGGTTC[C/T]TGACAAGGTTTTCAA | 55130 |
| rs748869503 | snp | C/T | | | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999094 | TGGGTTCCACCCGCC[C/T]CGGCCACCTGCTGCT | 55130 |
| rs748876959 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27908408 | GAAAAATGAATTATC[A/G]TCAGAGCCATCTCTC | 55130 |
| rs748889786 | snp | A/C | 5.16587e-05 | 0.00508199 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944470 | GTGGCGAATATGTAA[A/C]CCGTGCTATGTTTTT | 55130 |
| rs748891400 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27849821 | AGGGCAGCATGGCCA[A/G]GTGCAGTAATTTTCA | 55130 |
| rs748903465 | in-del | -/TTC | | | intron-variant, upstream-variant-2KB, cds-indel | ARMC4 | GRCh38.p7 | 10:27982010 | GTTTGTCACACTCTG[-/TTC]TTCTGTCTGTGGCAT | 55130 |
| rs748917272 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27873047 | GAGCAACAATTGGTC[A/T]ATTGAGGGATTCAAC | 55130 |
| rs748930634 | in-del | -/AA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27924003 | AAGAAAGAAAGAAAG[-/AA]AGAAAGAAAGAAAGA | 55130 |
| rs748941013 | snp | A/G | 1.64825e-05 | 0.00287071 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27944825 | ACTCACCTTACATTT[A/G]ACTTCATCGGTTTCA | 55130 |
| rs748942824 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27899360 | ACACCACCAAAGCCA[C/T]GGGTTTCAAGCACAA | 55130 |
| rs748946300 | snp | A/G | 1.71755e-05 | 0.00293044 | intron-variant | ARMC4 | GRCh38.p7 | 10:27812662 | AGAAGGGACACAAGA[A/G]TAAAAACATTAATCT | 55130 |
| rs748953101 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27861420 | GTCATTAGCTCAAGG[C/T]TAGATTTTCTTTAGA | 55130 |
| rs748958486 | snp | C/G | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27959128 | GACTGCTTGAGGCCA[C/G]GAGTTCAAGATCAGC | 55130 |
| rs748990000 | in-del | -/TCT | 1.64898e-05 | 0.00287135 | cds-indel | ARMC4 | GRCh38.p7 | 10:27995000 | AAAACAAATTTTGCC[-/TCT]TGAGGATGTTTATAG | 55130 |
| rs749013446 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27958566 | ATTAACTCACTCTAC[C/T]TCCCCCCTTTTATTG | 55130 |
| rs749017415 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27965230 | CCTCATAGGAAAGGA[G/T]GTCTAATCTGAAGAG | 55130 |
| rs749019198 | snp | A/G | 3.29679e-05 | 0.00405991 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27995071 | CGCTTCATTTAGAGG[A/G]GTGATTTCGAGGATT | 55130 |
| rs749034282 | snp | C/G | 1.64917e-05 | 0.00287151 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27812579 | ATACAACCAGCTGCA[C/G]CTTCCTGGAGATCCT | 55130 |
| rs749046419 | in-del | -/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27956965 | TCCTGTTTCACAAAA[-/G]GGCTCTCCACCTACC | 55130 |
| rs749047461 | snp | A/C | 2.23316e-05 | 0.00334146 | synonymous-codon, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27985069 | CAGATCCAATTGCTT[A/C]AGCAGCATAGCAATC | 55130 |
| rs749077832 | snp | C/T | 3.30426e-05 | 0.0040645 | intron-variant | ARMC4 | GRCh38.p7 | 10:27981628 | TTAACATAAGAACAA[C/T]TGTAAGAAGCTGATC | 55130 |
| rs749094816 | snp | A/G | 1.76905e-05 | 0.00297404 | intron-variant | ARMC4 | GRCh38.p7 | 10:27981440 | ACATAATGCTATGAA[A/G]GCTCAAAAGAAACCA | 55130 |
| rs749098637 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27944767 | GCTAAGAAGAGAGCC[C/T]AGGAAGGTGGGAACA | 55130 |
| rs749099095 | in-del | -/ATAA | 0.0026455 | 0.0362733 | intron-variant | ARMC4 | GRCh38.p7 | 10:27853366 | GGCGAGACTCTGTCT[-/ATAA]ATAAATAAATAAATA | 55130 |
| rs749119566 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27932261 | GGCAAAATCATCTAA[C/T]ACAAAGCCTATCTTA | 55130 |
| rs749134925 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27817692 | TATGACTGAGTAGGC[A/G]TTCTATGGCATATAT | 55130 |
| rs749140530 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27844547 | GAGCCTCTAAACCCA[C/T]GCTCCTTGAGTCCTT | 55130 |
| rs749153819 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27887700 | ATTCACAAATATGTG[G/T]AAATTAAACAACACA | 55130 |
| rs749194113 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27861132 | AAGTAGCTGAGATTA[C/T]AGGTGCCCGCCACCA | 55130 |
| rs749209882 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27920557 | GATTAAATGATTCAC[A/G]TAATTACTCTCCATT | 55130 |
| rs749218788 | snp | A/G | 3.30273e-05 | 0.00406356 | missense | ARMC4 | GRCh38.p7 | 10:27907752 | GGGACCACAACAAAC[A/G]AACTCCATCTAAGCG | 55130 |
| rs749228046 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27918303 | AACGCAAGAATGCAT[A/G]AAAAAGGTAATGCAA | 55130 |
| rs749239718 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27986553 | GCATAAAAAGAGGTT[A/G]CCATCCTGAGGTTAG | 55130 |
| rs749241584 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27921209 | CGAAATTTGGAGGAT[C/T]GCTTGAGCCCAGGAG | 55130 |
| rs749242913 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27868745 | GCTTAATACCTAGGT[A/G]ATGGGTTAATAGGTG | 55130 |
| rs749249602 | in-del | -/AT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27945432 | CATACTGGAACCTAG[-/AT]AGTAGGTGGTTTGAG | 55130 |
| rs749252511 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27951837 | TCCAGCACTTTGGGA[A/G]GCCAAGGCAGGTGGA | 55130 |
| rs749274616 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27943751 | AGTGAGCCAAGATCG[C/T]GCCACTGCACTCCAG | 55130 |
| rs749286883 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27942297 | TCTTAGTTGTTTTGA[G/T]GAATCTTTCTTAAAT | 55130 |
| rs749317856 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27858822 | TTTTTTTTTTTTTTG[-/T]AGACAGAGTCTCGCT | 55130 |
| rs749319028 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27966300 | GTGACTTAAACTTAA[C/T]TCAAAGATTCCAGAT | 55130 |
| rs749344652 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27929656 | AATCCTGTATGCTTA[C/T]GAATATGATATTGCC | 55130 |
| rs749360313 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27858328 | GAGGTCGAGAGAGAC[A/C]ATCTCCAGGTTGCAT | 55130 |
| rs749398179 | snp | C/T | 1.64789e-05 | 0.0028704 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27940641 | CAGCAGCCGAGCCAA[C/T]AGAGGAATGCCCCCA | 55130 |
| rs749399768 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27941687 | AAGCAGTATGTCAGG[A/T]TGCCCCATGGAGGAA | 55130 |
| rs749413387 | snp | C/T | | | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27995857 | TTCCCTGCCTGTATA[C/T]CCTGCCCAGATGACA | 55130 |
| rs749421035 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27865383 | GTCCTCAAATGTGCA[C/T]GTCTCCACAAGTCTG | 55130 |
| rs749424172 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27897159 | GTTTTCCCATCCCCT[A/T]CCCACCCGCCTGCCT | 55130 |
| rs749426111 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27881711 | AATTCTATGTTTATA[C/T]AACTAAAACCACTTT | 55130 |
| rs749432215 | snp | C/T | 1.66574e-05 | 0.0028859 | missense, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27961654 | GGTCAGGTGGTTCTT[C/T]ATCTTCCTCACTTTC | 55130 |
| rs749436999 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27966176 | GTGTGTAAAACACTA[C/T]GATTATGCTCTCTGG | 55130 |
| rs749438430 | in-del | -/GT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27969616 | CAATCAGAGGAGCCA[-/GT]GTCTCCCCTCTCCAC | 55130 |
| rs749461006 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27815188 | TATCCAAGGCCCACC[-/A]ATCCACTTGTATTCT | 55130 |
| rs749464912 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27814101 | ATGAAAAATTAGGCT[C/T]ACAGACAATTTGAAG | 55130 |
| rs749467088 | snp | C/T | 1.65075e-05 | 0.00287289 | missense, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984282 | GTCATGGGACTTAAA[C/T]TTATTTCTCTGAAAT | 55130 |
| rs749486825 | snp | C/T | 1.64773e-05 | 0.00287026 | missense, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27936769 | ATTTCCATATAGCCC[C/T]TGTGACAGCAGCTAA | 55130 |
| rs749514705 | in-del | -/T | 6.59071e-05 | 0.00574014 | frameshift-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27936755 | TTTGCTGATGGAACA[-/T]TTCCATATAGCCCCT | 55130 |
| rs749527160 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27961882 | CCAGCCTGGACAACA[C/T]AGCAAGACTCTGTCT | 55130 |
| rs749572910 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27914218 | TGCATTGAAACACAT[C/T]GAGAGGCACAAAATA | 55130 |
| rs749605741 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27936217 | GAGATAGATTTGAAA[A/G]TTAAAATAAATCAAA | 55130 |
| rs749613425 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27950104 | TGAGACTTGGAGAAT[C/T]GGCACCACTATCACA | 55130 |
| rs749615817 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27949203 | GTGTTGCATGCTTCC[C/T]ATTTGCCATGCTGGA | 55130 |
| rs749616521 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27902444 | ACAAGAAATAACTAA[G/T]ATCAGAGCAGAACTG | 55130 |
| rs749619634 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27814984 | CTTTCCAATGCCTAT[C/T]TTAAATCTTCCTTCT | 55130 |
| rs749634808 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997680 | AGAAAACCTCAGGGT[A/G]GCCTATGACAATCCA | 55130 |
| rs749649212 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27834442 | TCTCACTTCCCATTG[C/G]TGATAACCTAATCAT | 55130 |
| rs749682576 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27852019 | TGATAATAAAATGGA[A/G]CACCATGTTTAAAGT | 55130 |
| rs749701407 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27867267 | CACTGGAAAGTTCCA[C/G]AACAGCAGCAGAAGC | 55130 |
| rs749701787 | snp | C/G | 1.65282e-05 | 0.00287469 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984155 | TGAAAATGTAAATAA[C/G]ATAAAATGAGCCTGA | 55130 |
| rs749707046 | snp | A/C | 1.65091e-05 | 0.00287303 | missense, intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27971244 | TGCGGAGGGCAGCTG[A/C]TTCTTCCTTCTTGGG | 55130 |
| rs749709863 | in-del | -/AAAG | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27930644 | AAAAAAAAAAAAGAA[-/AAAG]AAAAAGGCAAACAAA | 55130 |
| rs749731316 | snp | C/T | 1.67792e-05 | 0.00289643 | intron-variant | ARMC4 | GRCh38.p7 | 10:27935292 | GAATTGGTTTTTGTA[C/T]AAGGTTTGCTAAAAA | 55130 |
| rs749759910 | snp | C/T | 4.45484e-05 | 0.00471934 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944219 | AACATCACGGCTACT[C/T]ACCAGTTTGGTGATA | 55130 |
| rs749773887 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27835824 | CAGCTACCTCGGGAG[C/G]CTGAGGCAGGAGAAT | 55130 |
| rs749814633 | snp | A/G/T | 6.61785e-05 | 0.005752 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27944286 | AACTTGGCAACATTC[A/G/T]CGATAGTCTCGGCTG | 55130 |
| rs749831255 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27893625 | TTACTTGCAAAAGCA[C/T]TGTAGTTGAAAACAA | 55130 |
| rs749833861 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27937004 | TCATTTTCGAAAGAT[A/G]CCTCCAAGTAAAATA | 55130 |
| rs749836151 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27891215 | ACTGGCCTCATCCAT[A/T]CTCAGTCCTCAACAT | 55130 |
| rs749841237 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27903702 | CTCTCATTCACAATT[A/G]CTACAAAGAGAATAA | 55130 |
| rs749842787 | snp | A/T | 1.65121e-05 | 0.00287329 | missense | ARMC4 | GRCh38.p7 | 10:27940564 | ACTGGCATGAGTACC[A/T]CTGATGCACACTCTT | 55130 |
| rs749868716 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27973328 | GCAAAACCCCATCTG[C/T]ACCAAAAATAAAATA | 55130 |
| rs749931933 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27863789 | ACAAATCATCATGTT[A/G]CACAGATCTGACAGC | 55130 |
| rs749944281 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27826395 | TTGCCCGGTCATCCA[C/G]CCAGGTGTCTCTCTC | 55130 |
| rs749946940 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27995296 | CTGCTTATTAATCTT[C/G]GAAGATTCTTTTAAC | 55130 |
| rs749958564 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27839463 | TCACCTGTTGCTATG[A/G]AGTTTTTGAGTGCAA | 55130 |
| rs749990747 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27881269 | AATTTATTTGATTCC[A/G]CATGTCATTAACCCT | 55130 |
| rs749998513 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27862970 | TGTTCTATAAAGTAA[C/T]TGCAAACACTGAATC | 55130 |
| rs750013814 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27890820 | TCTAATCTTTTAGGA[-/T]TTTTAGGATCTGGGG | 55130 |
| rs750046470 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27833829 | CGTGCAAGTCCTGGG[C/T]GACTACAGACAGCAA | 55130 |
| rs750052754 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27901321 | GAAGGAAGCACTAAA[C/T]TTGGAAAGGAAAAAC | 55130 |
| rs750067564 | in-del | -/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27843625 | AGAAAAAAATTAGCT[-/G]GGTGTGGTGGCATGT | 55130 |
| rs750072681 | snp | A/G | 6.59207e-05 | 0.00574073 | missense, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27944949 | GCAATCACTGTAGCT[A/G]TTTGATTTCCTCCCT | 55130 |
| rs750081562 | snp | G/T | 3.29647e-05 | 0.00405971 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27860745 | CAGATAACGCACTAG[G/T]GGAGCCACTGCTTTG | 55130 |
| rs750082472 | snp | C/T | 1.64841e-05 | 0.00287085 | missense, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984228 | GTTTGGTTTCCTTTT[C/T]CTGAGAAACGTTTGA | 55130 |
| rs750087922 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27827680 | TTGCAACCACCATTC[C/T]CTCTCCCTGGACGAC | 55130 |
| rs750102716 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27947262 | AGCCAGTACTTCCAT[C/T]TCCTCTTTTAAAAAA | 55130 |
| rs750104712 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27913775 | CTGCAAATCAAAACC[A/G]CAAGAAGATACTATC | 55130 |
| rs750117236 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27882605 | TATTCAAGAAAAATG[A/C]CTGAATCTCAGTAAG | 55130 |
| rs750148083 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27813610 | GTGCAAATGTGGATG[A/G]TGCCAAAAAACGAGG | 55130 |
| rs750166796 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27949757 | GGCCGCTGGCTGGAG[C/G]GGGCAAGCGTGGATG | 55130 |
| rs750178697 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27935531 | CTCTACTAGGGTTTT[C/T]TCCCCCTATCTTCCA | 55130 |
| rs750186207 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27833961 | GCCGAGAAAGGACAG[C/T]GGTGAAGGTTCCACA | 55130 |
| rs750299934 | in-del | -/A | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27998168 | GCTCTGAGATCTATG[-/A]AATGTGGTTGGTAAC | 55130 |
| rs750317578 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27883065 | CCTGGGAATCTAAAA[A/G]GCTACATACATGTGT | 55130 |
| rs750331607 | snp | A/T | 2.83074e-05 | 0.00376203 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944196 | GGCTGGCACTAGATG[A/T]CGATGACAACATCAC | 55130 |
| rs750332533 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27876472 | AACTCCAGCAGACCT[A/G]CAGCTGAGGGTCCTG | 55130 |
| rs750349451 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27933913 | AGATACGTGGTTAGA[C/T]GAAGCCCCCTGATAG | 55130 |
| rs750386349 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27989205 | TGTTAAGCCATTAGG[C/T]TTGGGGCAATGTGTT | 55130 |
| rs750387542 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27890573 | ATCCCTTTGTAGACT[A/G]GCAGCCTCTATTGCA | 55130 |
| rs750407685 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27905727 | ACACATCTACAACCA[C/T]CTGATCTTTGACAAA | 55130 |
| rs750411885 | snp | G/T | | | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27936652 | ATTGACTCCTTACTA[G/T]AATGGCATTAAATGA | 55130 |
| rs750439475 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983609 | TATAAAGTGGAATGG[A/G]TCACTTTGAAGCCCA | 55130 |
| rs750518822 | in-del | -/G | 1.64838e-05 | 0.00287083 | frameshift-variant | ARMC4 | GRCh38.p7 | 10:27935065 | TTGTAACATTCACAA[-/G]AAGAGCTTGGTTTAT | 55130 |
| rs750520389 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27861892 | TTGAATTTCTGCTCT[A/G]TGACTTTTCTGCCAA | 55130 |
| rs750563454 | snp | C/G | 2.77327e-05 | 0.00372365 | missense | ARMC4 | GRCh38.p7 | 10:27985116 | TTTCAGGATCATCAT[C/G]TCTGGTAATTTTGCC | 55130 |
| rs750579435 | in-del | -/G | | | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27857877 | AGCTGCAGCAGGAAT[-/G]TTTGTACAACTGGAA | 55130 |
| rs750585602 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27843244 | CTTAAAATAAAAACA[A/G]CCTATCTGCAACAAA | 55130 |
| rs750587404 | in-del | -/AAG | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27929764 | GGCTTGTGTCATTAA[-/AAG]AAGATGCAGAGAAGT | 55130 |
| rs750589427 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27911600 | AGGCCACAGAGCTTC[A/T]CCCCGTTATGCACTT | 55130 |
| rs750607142 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27869180 | GAGCACAAGAACAAA[C/T]AAAGATAATGGATAA | 55130 |
| rs750608944 | in-del | -/G | | | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999675 | TGGGAATATTGAGGT[-/G]GGGGGGGGATGGGGA | 55130 |
| rs750614997 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27933736 | TGAATAGCAAAGTGC[A/G]TTTCAAAAACATAAA | 55130 |
| rs750615426 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27897387 | CATCTTTTCCTCAGA[C/T]GATGTTATTCCCATG | 55130 |
| rs750620847 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27887328 | ATACATGCACCAAAC[A/C]TGAAAGTTCTGAAAT | 55130 |
| rs750662322 | snp | A/G | 1.81926e-05 | 0.00301595 | intron-variant | ARMC4 | GRCh38.p7 | 10:27985219 | TCTGTTAGCTGCCAA[A/G]AAAAAAAAAAAGGAG | 55130 |
| rs750695430 | snp | C/G | 1.65132e-05 | 0.00287339 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944794 | AACAAGACTCCGCAT[C/G]CAAGGTGACAGAGCC | 55130 |
| rs750706164 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27923951 | CCTGTCTAATGAAAG[-/A]AAGAAAGAAAGAAAG | 55130 |
| rs750715208 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984556 | ATATTAGAAAATGAA[C/T]ATGCTTTGGACTATA | 55130 |
| rs750722314 | snp | A/G | 4.94882e-05 | 0.0049741 | missense | ARMC4 | GRCh38.p7 | 10:27862516 | TCTTTTGCTATGTTG[A/G]TAATGGCAGCACATA | 55130 |
| rs750736227 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27831222 | CTATCAGAACAATTC[C/T]TTGTTCTTTTTTGAT | 55130 |
| rs750757328 | snp | A/T | 1.65329e-05 | 0.0028751 | missense, utr-variant-3-prime | ARMC4 | GRCh38.p7 | 10:27936870 | TCCCGGGTTTCCTTA[A/T]CTTCAGCACACTGCA | 55130 |
| rs750779558 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27952517 | AGATTTTCAGCCCCA[C/T]ATGCACTGGCTATTT | 55130 |
| rs750799868 | in-del | -/TTT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27938598 | GTATCTGTCTCTTCT[-/TTT]TTTTTCTTTTTTTTT | 55130 |
| rs750800986 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27817381 | ATTTCGAGGGTACAA[A/G]TGCAAATTTCTTACA | 55130 |
| rs750803109 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27828187 | TCTGAAGTTTCTAAG[G/T]CAAAAGTCAGAAGAC | 55130 |
| rs750811843 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27920602 | CTCAGTTAAATCTAC[A/G]TGCTTTAAAAGTATG | 55130 |
| rs750815975 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27916270 | ACATGGGGAACTAGA[C/G]CCTGAATGGGGTGAA | 55130 |
| rs750820541 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27832295 | GGGTCTCTCTGGTTT[C/G]ATGTTTCTCACACCT | 55130 |
| rs750880820 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27914314 | TTTCCATTTTAAAGA[C/T]GCCATTTTTTCTTTT | 55130 |
| rs750902239 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27942122 | TGCAGTATGGAAGTG[C/T]TCAGAAAGCCCGTAG | 55130 |
| rs750940039 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27940399 | TATATATATCACAGG[C/T]ACTGATTTAATTAAC | 55130 |
| rs750945009 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27939169 | CACGCATTCCTCTGG[A/C]TAGTCTTGGTAGGAG | 55130 |
| rs750961900 | snp | C/T | 1.68267e-05 | 0.00290053 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983834 | TTACGTTTTTAAAAA[C/T]TTACTTACACCATTT | 55130 |
| rs750965893 | snp | A/C | 6.65347e-05 | 0.0057674 | intron-variant | ARMC4 | GRCh38.p7 | 10:27907792 | CCTATCGTGGAACCC[A/C]AAATCATGATATAAA | 55130 |
| rs750972953 | snp | A/G | 1.68533e-05 | 0.00290282 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944453 | GAGAAAAAAAAAGAT[A/G]AGTGGCGAATATGTA | 55130 |
| rs750988855 | snp | A/C | 1.66665e-05 | 0.00288669 | intron-variant | ARMC4 | GRCh38.p7 | 10:27812631 | CCAGTAGAAGCTGTC[A/C]CACATAAGGAGGAGA | 55130 |
| rs751000239 | in-del | -/TG | 1.65833e-05 | 0.00287948 | splice-acceptor-variant, intron-variant | ARMC4 | GRCh38.p7 | 10:27944433 | TTTAATGAACCAATC[-/TG]TGTGAGAAAAAAAAA | 55130 |
| rs751066578 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27833067 | CCTTGCCTGGCCGTG[C/T]TTTTTGAAGTTTTTC | 55130 |
| rs751070849 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27981974 | AGGTTAGAATTTAAC[C/T]GTGGAAAAGCCTACA | 55130 |
| rs751071292 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27814647 | TGTTCTCATCATGAT[C/G]TCTTGTCCATGGGCT | 55130 |
| rs751075237 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27827801 | AAAATATTTTAATGG[C/T]TCCCCAATGTCAAAT | 55130 |
| rs751085100 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27831647 | TCTTATCTGCCATAC[A/T]GATGGCCTCCCTTGG | 55130 |
| rs751085155 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27961119 | TGTTTTATTAAACTT[C/T]ATAATAGTCCTGTAG | 55130 |
| rs751103161 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27866853 | ACTCCTCCCATTAGA[C/T]CCCACTCCAACACTG | 55130 |
| rs751131195 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27886545 | AATAAAAGGATTCTA[C/T]ACAGTAACTTGAAGC | 55130 |
| rs751140455 | snp | C/T | 0.00021435 | 0.0103503 | missense | ARMC4 | GRCh38.p7 | 10:27995000 | AAAACAAATTTTGCC[C/T]CTTGAGGATGTTTAT | 55130 |
| rs751158162 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27864987 | TGAAGGTAGGCACCA[C/T]GTGTTACTCAACTGA | 55130 |
| rs751168097 | snp | A/G | | | synonymous-codon, utr-variant-3-prime | ARMC4 | GRCh38.p7 | 10:27936854 | GTGCAGCCTAACGAG[A/G]TCCCGGGTTTCCTTA | 55130 |
| rs751193375 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27890847 | GGGGGCCAGATGGGT[A/G]CATACTTAGAACTAT | 55130 |
| rs751194510 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27911769 | GCCCCTCATACCACA[-/T]TTACTTTGCCTTGTA | 55130 |
| rs751222731 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27950571 | TACAAGGATGCTACA[C/T]ACATTCTTCTAATTG | 55130 |
| rs751223362 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27949846 | AGGGTGACTCATCAC[A/G]AACCATAAAGAAACG | 55130 |
| rs751228046 | snp | A/G | 1.7939e-05 | 0.00299486 | intron-variant | ARMC4 | GRCh38.p7 | 10:27994900 | GATATCAAATCCTAG[A/G]AGCAAGTAACTGGCT | 55130 |
| rs751289620 | snp | C/T | 1.64808e-05 | 0.00287057 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27860751 | ACGCACTAGTGGAGC[C/T]ACTGCTTTGTGCTCA | 55130 |
| rs751327078 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27974289 | AATTAGATCCCACTT[A/G]TCAATTTTTGCTTTT | 55130 |
| rs751344100 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27923891 | GAGTCCAAGGCTGCA[C/G]TAAGCTATGATTACA | 55130 |
| rs751363822 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27836193 | ATATACACAGTTGAA[A/T]ACATATGCATGTATA | 55130 |
| rs751406313 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27965934 | AGCCTTCATGCTTAT[A/G]TCAATTCATTCTCAT | 55130 |
| rs751412469 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27907888 | ATATTTTGCTTAGAA[-/T]TTTTTTTTTTTTTTG | 55130 |
| rs751415515 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27878728 | GTCGTCAAAAGTATA[C/T]TTAATGAATTAAATC | 55130 |
| rs751431302 | snp | A/G | 2.31506e-05 | 0.00340217 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984993 | TGGCTCAATACAATA[A/G]AGGTTCCTTTTTGAA | 55130 |
| rs751441822 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27958214 | TTATTGATGAATAAC[C/T]TGTGCAAATTTAAGT | 55130 |
| rs751458672 | snp | C/T | 1.69821e-05 | 0.00291389 | intron-variant | ARMC4 | GRCh38.p7 | 10:27961526 | CTTTGGGAAAGTATT[C/T]TAAATGAACATTGCA | 55130 |
| rs751477980 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27861271 | TGCTGAGATTACAGG[C/T]GTGAGCCACTGCACC | 55130 |
| rs751520156 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27910823 | CATCAGGGGAAGTTA[C/T]GTTCTATCAAGTCAG | 55130 |
| rs751533290 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27877656 | AACTGTCTTTCACCA[A/G]TGCTGAACGACTGGG | 55130 |
| rs751547513 | in-del | -/AAAAAAAAAAAAAA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27943796 | GTGAGGCTCTGTCTC[-/AAAAAAAAAAAAAA]AAAAAAAAAAAAAAA | 55130 |
| rs751570102 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27933853 | ACACTGGAGACTAAG[A/G]TTCCAATAACCAAAT | 55130 |
| rs751573487 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27929537 | ACTGGTATCTTTTAG[C/T]CATAGTTTTACTATT | 55130 |
| rs751601634 | snp | G/T | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984969 | GGCTGGAGTTCAGTG[G/T]TGCAATCTTGGCTCA | 55130 |
| rs751613630 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27986278 | GGAATGGCATAAACC[C/T]GACTACCAAATTGCC | 55130 |
| rs751670890 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27831342 | CTGCCCAAATCCACC[A/G]TTATAGACCCAGGAA | 55130 |
| rs751718086 | snp | A/G | 5.06359e-05 | 0.00503144 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27944257 | GCTGCCTCACCACCC[A/G]CCGTGCTCTTTTAAA | 55130 |
| rs751721941 | in-del | -/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27919381 | TGCTCAAAAGGAAGT[-/C]TTAATGCTTACTGGG | 55130 |
| rs751736986 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27978608 | CACCAGCTTGGCCAA[C/T]ATGGGAAAACCCCAT | 55130 |
| rs751745036 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27869778 | GACCTTAAGTGATCC[A/G]CCTGCCTCGGCCTCC | 55130 |
| rs751755800 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27888462 | TGTTGGCTATTTGTA[C/G]GTCTTCTTTTGAAAA | 55130 |
| rs751804600 | in-del | -/AGAA | | | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27996098 | AATAAGAGCCAAGTT[-/AGAA]AGCACGTTCTGACTT | 55130 |
| rs751809920 | snp | C/T | 3.29891e-05 | 0.00406122 | missense, intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27971223 | TGTCTGAACCAGAAA[C/T]GTCTTTGCGGAGGGC | 55130 |
| rs751814479 | snp | C/T | 3.44513e-05 | 0.00415024 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940027 | GAATAAAAACCTACA[C/T]ATTTATGTGTTCAAG | 55130 |
| rs751819652 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27981169 | CAGGAAGTCAGGGAA[G/T]AAGGAATGGGGAATT | 55130 |
| rs751839031 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27859742 | TCTAAGTATTTTTAT[A/T]CTTATTGCCAGCAAA | 55130 |
| rs751845596 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27889401 | GGACACAGCATATCA[A/G]ATTTGACATCAGAAT | 55130 |
| rs751858711 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27833506 | AATAAACAATTTAAA[C/T]TCTGTGGCTTATGTG | 55130 |
| rs751861023 | snp | C/T | 1.67156e-05 | 0.00289093 | intron-variant | ARMC4 | GRCh38.p7 | 10:27907658 | GACTTGCAGTCCGTT[C/T]TTACCTTTGCATTTT | 55130 |
| rs751874534 | in-del | -/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27882172 | ACCTTGTCATAAAAA[-/G]AAAAGAAAGAAAGAA | 55130 |
| rs751881899 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27818515 | CAGCCAGGTCATCAC[A/G]ATGAATAATGCCAGT | 55130 |
| rs751906807 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27939510 | CACTTGAAGCCAGGG[G/T]TTTGAGACCAGCCTG | 55130 |
| rs751908192 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27940876 | CATTCTTCAATAGCT[A/T]CAGTGTTCCTTACCA | 55130 |
| rs751908696 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27955390 | ATACAACAGCAAGTT[A/C]TGCAGGCCTCCTGGG | 55130 |
| rs751933337 | in-del | -/TC | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27962118 | AGGTGAATAAACCTG[-/TC]TCTATTGCAGGTGCA | 55130 |
| rs751989972 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27851862 | AAACATGAAGGAAAC[C/T]ACACAAGGCCCATCA | 55130 |
| rs752008403 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27819374 | GGGGTGAGAGAGATA[A/T]ACTATGAAAGATTAA | 55130 |
| rs752011146 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27826699 | CCTCCTGCCTCCCTC[G/T]CCACATCCTCTGGAA | 55130 |
| rs752029987 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27909777 | GAGTCGAGATTGCAC[A/C]ACTGCACTCCAGCTT | 55130 |
| rs752041055 | snp | A/C | 0.000102072 | 0.00714322 | intron-variant | ARMC4 | GRCh38.p7 | 10:27987337 | TCCCCACTTTCCCAG[A/C]AAGATTGTTTCTAAA | 55130 |
| rs752067812 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27882766 | AGGGACAGAATAGGT[G/T]TGGAGCCCCACAAAA | 55130 |
| rs752072117 | snp | A/G | | | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27987413 | CTTGGGCTTCCTTCA[A/G]CTTCCCAGTTTTGGC | 55130 |
| rs752081268 | in-del | -/TGATGCCTAAGTTTCTTTCCAGGCTACATTTACCAAACTTGGACT | 1.66263e-05 | 0.00288321 | cds-indel | ARMC4 | GRCh38.p7 | 10:27862597 | CCAAACCACCAACAA[lengthTooLong]AGGAACGAACCATTT | 55130 |
| rs752089999 | snp | C/T | 1.64789e-05 | 0.0028704 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27944900 | CAACTGGCAGGTTTC[C/T]TGAGCTAAGCTGAAA | 55130 |
| rs752116622 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27980752 | TGGTGTGGCCCCCGT[A/G]GAAAACAGGTTGGCA | 55130 |
| rs752137249 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27942095 | TGAACACAGATGCAC[A/G]ACAATAAATGATGCA | 55130 |
| rs752140248 | snp | C/T | 0.000132461 | 0.00813714 | missense | ARMC4 | GRCh38.p7 | 10:27939923 | CCATGGCGCAGTGCT[C/T]CTGCAGCTGCTCATT | 55130 |
| rs752147402 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27961112 | TCAAGTGTGTTTTAT[C/T]AAACTTTATAATAGT | 55130 |
| rs752161140 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27950818 | ATTGGAATGTTCTAG[G/T]CATTGCAATGCAGAA | 55130 |
| rs752214409 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27949962 | GGGTCATCATTTGAA[A/G]TTATTATCAGAGCCC | 55130 |
| rs752216366 | in-del | -/AAG | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27854858 | TTGATTGAGCCACAT[-/AAG]AATGTGAATTAATAC | 55130 |
| rs752218614 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27882117 | GAGGTTGCATTGAGC[C/T]ACAATTCCCCATAGC | 55130 |
| rs752247912 | in-del | -/A | | | downstream-variant-500B, intron-variant | ARMC4 | GRCh38.p7 | 10:27811860 | GTCAAAGTGTAAAAC[-/A]AAAAAAACTCATTGC | 55130 |
| rs752301264 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27904180 | TTAGAAATTAACAAT[A/G]GCTTTCCACGTGATA | 55130 |
| rs752304416 | in-del | -/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27878832 | GATCCTTGTTCTGTT[-/C]CCAGTTGTTAACAAA | 55130 |
| rs752312221 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27903481 | AAAGCAATAAAGAGT[A/T]TTCAAATAGGAAGAG | 55130 |
| rs752348839 | snp | A/C | 1.64836e-05 | 0.0028708 | stop-gained | ARMC4 | GRCh38.p7 | 10:27995046 | CAAACACAATAATTT[A/C]TTTCAATATCGCTTC | 55130 |
| rs752349771 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27836289 | CATAGAACTGATAAG[A/G]ACACAGAGACCAGTG | 55130 |
| rs752364240 | snp | A/G | 1.66443e-05 | 0.00288477 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940810 | AGTAGAGCAACCTAT[A/G]ATAATAGATAAATCC | 55130 |
| rs752394610 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27937908 | TACGATTGTTATGGG[A/C]CAAATTGTGTCCCCT | 55130 |
| rs752423499 | snp | A/T | 1.64841e-05 | 0.00287085 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27935069 | AACATTCACAAGAAG[A/T]GCTTGGTTTATTCCA | 55130 |
| rs752431336 | snp | A/C | | | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27996194 | TAGCACTTATTGATA[A/C]AATCTTTCTTCCAGA | 55130 |
| rs752449983 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27814419 | ATTTAGAAGGTTGTA[A/T]ATGAGAATATCTTGT | 55130 |
| rs752474303 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27880906 | TTCATTGGTGGGTGG[C/G]AATGGAAGGCAGCAT | 55130 |
| rs752476207 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27862087 | CATTTGATTTCTAAC[A/G]TTGGCATGAAGAACC | 55130 |
| rs752477723 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27927531 | TCAAAGTTAAAATAC[C/T]GTTTTCTGAAACTTA | 55130 |
| rs752503685 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27901653 | GCAAAAAAAGCAGGG[A/G]TTGCAATCCTAGTCT | 55130 |
| rs752505169 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27978601 | AGTTTGACACCAGCT[G/T]GGCCAACATGGGAAA | 55130 |
| rs752524292 | snp | C/T | 2.28564e-05 | 0.00338048 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27985005 | ATAGAGGTTCCTTTT[C/T]GAAAAAGACTCACAA | 55130 |
| rs752529553 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27879257 | TGAGGTACCATTGTG[C/T]AACCAGAGGCTTACA | 55130 |
| rs752544107 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27838874 | AACAAAAAAAGCTGC[A/G]GGACATAGCTACTGT | 55130 |
| rs752546092 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27837615 | TGCTGTAAATGGAAC[A/G]TTAGGGTGCTTTTCT | 55130 |
| rs752561154 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27946602 | ATTTCTTGACTGTAC[C/T]ACAATAGGGAACTTG | 55130 |
| rs752577298 | snp | C/T | 1.64988e-05 | 0.00287213 | synonymous-codon, utr-variant-3-prime | ARMC4 | GRCh38.p7 | 10:27936845 | AAGTCCTCCGTGCAG[C/T]CTAACGAGGTCCCGG | 55130 |
| rs752581329 | snp | C/T | 3.3305e-05 | 0.00408061 | missense, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27961650 | CGATGGTCAGGTGGT[C/T]CTTCATCTTCCTCAC | 55130 |
| rs752595437 | snp | C/T | 8.2411e-05 | 0.00641862 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27940734 | ACAGCGAGCCACTTC[C/T]ACGTCTCTGGCCTCA | 55130 |
| rs752596897 | in-del | -/TA | 0.000182063 | 0.00953932 | intron-variant | ARMC4 | GRCh38.p7 | 10:27934976 | GTTCTCCCTAACACT[-/TA]TATAAAATCTTTCCA | 55130 |
| rs752627647 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27932904 | CTTTGTTTGGTTACC[A/G]TTATAAATCCAGTGG | 55130 |
| rs752631264 | snp | A/C | 1.64819e-05 | 0.00287066 | missense | ARMC4 | GRCh38.p7 | 10:27860768 | CTGCTTTGTGCTCAC[A/C]GAAGGCCACTCTATT | 55130 |
| rs752639302 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27844430 | ATAAAGCAGAGTTTC[C/T]CAACCAGGCTCAGTC | 55130 |
| rs752659064 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27922229 | CAATAAAAGAACTTT[A/G]TATCTAGCAAGGCTG | 55130 |
| rs752659072 | in-del | -/AA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27995201 | TCAGAGCAGAAAGAG[-/AA]AGAGACAACAGCGTC | 55130 |
| rs752667106 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27954574 | TTTTTAACATTGTCA[C/T]GTTTCAGTCGTTAAG | 55130 |
| rs752682843 | snp | A/G | 1.68695e-05 | 0.00290422 | intron-variant | ARMC4 | GRCh38.p7 | 10:27860858 | TATTCTGTGCAAGGG[A/G]AAATGAAATGGGATC | 55130 |
| rs752697932 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27858411 | TAATTTACAAAAAAG[C/T]ACCCTGTTCTTTACA | 55130 |
| rs752722722 | snp | A/G | | | utr-variant-3-prime, intron-variant | ARMC4 | GRCh38.p7 | 10:27812345 | AACAAAAGTCTCCAT[A/G]CAATTTTCAGATGAA | 55130 |
| rs752728393 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27833728 | TTCCTGGAAATGCAG[A/G]AGTAGACAAGAAAGG | 55130 |
| rs752737561 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27972168 | GGTATTCAAGGTATA[C/T]TGTTGTAAGTTTCTT | 55130 |
| rs752759930 | in-del | -/GT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27913666 | CCCCATTGAAAAGTG[-/GT]CAAAGCACATGAACA | 55130 |
| rs752762752 | snp | C/G | 1.65573e-05 | 0.00287721 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27944428 | GTATTTTTAATGAAC[C/G]AATCTGTGTGAGAAA | 55130 |
| rs752767697 | snp | A/G | | | missense, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27936754 | CTTTGCTGATGGAAC[A/G]TTTCCATATAGCCCC | 55130 |
| rs752791062 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27970832 | AAAAAGTTAGCCAGG[C/T]GTGGTGGCATGTGCC | 55130 |
| rs752833928 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27913201 | ATTACGTGTCGCGGG[C/G]GTTTGGTGTACAGAT | 55130 |
| rs752850426 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27909254 | ATATTTAACTGTATA[C/T]TGCTGGACAGAAATA | 55130 |
| rs752875026 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27977892 | CAGTTAATGATGAGT[A/C]TGTGGAAGAACTGGG | 55130 |
| rs752882309 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27890240 | GGAAGAAGAGGCCAT[C/T]TGGGGTCCCAGTCAG | 55130 |
| rs752884686 | in-del | -/CT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27981388 | AAATAGGCAAAATTA[-/CT]GTTTTTCTTGTACCA | 55130 |
| rs752897216 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27897001 | AAATGGCTACAACCA[C/T]GACCGCCTAATTCCT | 55130 |
| rs752940728 | snp | C/T | 2.57443e-05 | 0.00358769 | intron-variant | ARMC4 | GRCh38.p7 | 10:27971337 | AAAAAATGAGAATAA[C/T]TTTTAATGATATCTG | 55130 |
| rs752942421 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27937123 | CAATTCTCCCAAGCC[A/G]GTTTTGAGATAGCCT | 55130 |
| rs752989295 | snp | C/T | 1.65531e-05 | 0.00287686 | missense | ARMC4 | GRCh38.p7 | 10:27907677 | CCTTTGCATTTTTGA[C/T]GCATGGACAGAGTGC | 55130 |
| rs752990927 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27923438 | AAAAGTCATAATTCA[C/T]AACCATTAGAAACAT | 55130 |
| rs753001008 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27955878 | CCTGCCAGGGAGGAG[C/T]TCTGGGAGTCCCTTC | 55130 |
| rs753002528 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27842435 | TGACCAAACTTTTCA[A/C]GAGATTGTGCCTCCA | 55130 |
| rs753002909 | snp | C/T | 1.64819e-05 | 0.00287066 | missense, synonymous-codon, intron-variant | ARMC4 | GRCh38.p7 | 10:27812535 | ATCTTGCCTTCTCTG[C/T]AGCAAGAGCCAGCCT | 55130 |
| rs753005082 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27821065 | GATTATAGGCGTGAG[A/C]CACCGTGCCCAGCCA | 55130 |
| rs753027491 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27995546 | TTTGTTCACAGCTCT[G/T]TTGGGAGCCAGCAGT | 55130 |
| rs753043076 | snp | A/C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27930552 | GAATGGCGTGAACCC[A/C/G]GGAGGCGGAGTTTGC | 55130 |
| rs753060546 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27828104 | GGGAGGTTAAATTCC[A/G]TGAAAGATGAAAACA | 55130 |
| rs753101612 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27934967 | CTCCCAAGTGTTCTC[C/T]CTAACACTTATATAA | 55130 |
| rs753113912 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27845837 | AGAAGGCCATTACAT[-/A]GATGGTAAAGGGATC | 55130 |
| rs753122640 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997412 | GTTTTGGTAATCTTA[C/T]AAAGATTGCTTCTTG | 55130 |
| rs753124728 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27875261 | GCCCTTCATCTAATC[-/T]TTTTTTTGAAGGTTT | 55130 |
| rs753177934 | snp | A/G | 5.4736e-05 | 0.00523116 | intron-variant | ARMC4 | GRCh38.p7 | 10:27987568 | AAAAATAAAAAATTG[A/G]AAGCTTCATGCTACC | 55130 |
| rs753179587 | snp | A/G | 0.000148509 | 0.00861582 | missense, intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27971232 | CAGAAATGTCTTTGC[A/G]GAGGGCAGCTGCTTC | 55130 |
| rs753207222 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27886649 | TGTAACTCCACTTTT[G/T]ATTTTCTACAGGATT | 55130 |
| rs753216418 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27957835 | GTATTAATGAGCTCG[-/T]TTAAATCTTTTTTTT | 55130 |
| rs753220366 | snp | A/G/T | 3.3076e-05 | 0.00406659 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940555 | GGAAGCAGAACTGGC[A/G/T]TGAGTACCTCTGATG | 55130 |
| rs753236178 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27958667 | TTGCTACAATAATAA[C/T]AAGCAATAGAAATGA | 55130 |
| rs753238409 | in-del | -/CA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27835925 | GAGTGAAAATCCCAT[-/CA]AAAAAAAAAAAAGGA | 55130 |
| rs753254063 | in-del | -/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27835925 | GAGTGAAAATCCCAT[-/C]AAAAAAAAAAAAAGG | 55130 |
| rs753254983 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27814864 | CCTGCGGGAGGCATA[C/T]GTCAACAACAAGGCA | 55130 |
| rs753260008 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27993376 | GATTTCAGGCCGGGC[A/G]TGGTGGTTCACACCT | 55130 |
| rs753265688 | snp | A/G | 3.29987e-05 | 0.0040618 | missense | ARMC4 | GRCh38.p7 | 10:27987443 | CAATAAGTAACAAGC[A/G]TGACAGCTGCCCAAA | 55130 |
| rs753272733 | snp | C/G | 1.95242e-05 | 0.00312437 | intron-variant | ARMC4 | GRCh38.p7 | 10:27862657 | AAGATGGTATCAAAA[C/G]TAAACCTACATTTAG | 55130 |
| rs753277037 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27988472 | CCCCCAAGTAGCTGG[G/T]ACTAGAGGCACATGC | 55130 |
| rs753319235 | in-del | -/G | | | downstream-variant-500B, intron-variant | ARMC4 | GRCh38.p7 | 10:27811697 | GCCACTTTTTAAAAA[-/G]TACTTTGTGTGCTGA | 55130 |
| rs753341990 | snp | A/G | 1.64784e-05 | 0.00287035 | synonymous-codon, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27944932 | CCCTCATTGAACACA[A/G]CGCAATCACTGTAGC | 55130 |
| rs753387087 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27837814 | TGACTTGTCAACCAT[A/G]AGGATAAGCCATTGT | 55130 |
| rs753392647 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27881053 | CAGCAAACTACTTAA[C/G]TTCTCTAAGCTTCAA | 55130 |
| rs753404923 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27995638 | GAATACTGTTATCCC[A/G]ACTTTCTTACAGTGA | 55130 |
| rs753413760 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27991944 | CAATGAATGAGGTCA[C/T]GGGGACTGTTTTGAT | 55130 |
| rs753433896 | snp | A/C | 1.65007e-05 | 0.00287229 | stop-gained, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983962 | GTGGGGCTCGACATC[A/C]ATTTGAAAATTCATA | 55130 |
| rs753452463 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27893453 | CAACAGCTTGTCTAA[A/G]GGCGTAGCTGGTGCT | 55130 |
| rs753459570 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27926004 | AGTGAGACTCCAGCT[-/A]AAAAAAAAAAAAAAA | 55130 |
| rs753461796 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27928831 | CACAGCACTTATTAT[A/G]TGTCAGTCACTTTAC | 55130 |
| rs753477183 | snp | A/T | 1.65592e-05 | 0.00287738 | synonymous-codon, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983873 | TCCTCCTGCACTGCA[A/T]GTAATGCACAGAGTC | 55130 |
| rs753480648 | snp | C/T | 1.6552e-05 | 0.00287676 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27935252 | TTTGTATTCCCGAAA[C/T]CTAAGTTCATCATAA | 55130 |
| rs753492082 | snp | A/G | 1.71572e-05 | 0.00292888 | intron-variant | ARMC4 | GRCh38.p7 | 10:27995190 | CACGCACTACATCAG[A/G]GCAGAAAGAGAAAGA | 55130 |
| rs753494979 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27978848 | CCTCAACATGCTAAA[G/T]GTCATATAAGAAAAT | 55130 |
| rs753521915 | snp | C/T | 1.64833e-05 | 0.00287078 | missense | ARMC4 | GRCh38.p7 | 10:27935083 | GAGCTTGGTTTATTC[C/T]AACAAGGAGGTTCAC | 55130 |
| rs753548579 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27926168 | CACAAATGCAGCCAA[A/G]GGCAATATATAAATT | 55130 |
| rs753554135 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27992072 | TGGGGAGTAGACCAA[C/G]GGGCACGGTCAAGAC | 55130 |
| rs753595606 | snp | C/G | | | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999904 | GGGATATGAGGTATA[C/G]ATATTTGTCCTTTGT | 55130 |
| rs753602333 | in-del | -/T | 1.65743e-05 | 0.00287869 | frameshift-variant | ARMC4 | GRCh38.p7 | 10:27860839 | TGATGTCTCAATTTA[-/T]TGTTATTCTGTGCAA | 55130 |
| rs753603176 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27849494 | AGCATGGCACATGTA[C/T]ACATAGGTAAAAAAT | 55130 |
| rs753623632 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27864750 | GTTGTATGGGGGTGA[A/G]TGTAATGTCCACCAA | 55130 |
| rs753636750 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27900173 | GATACCCAGGCAAAC[A/T]GGATCTGGAGTGGGA | 55130 |
| rs753644971 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27960708 | TTTATGGGGTACAAT[A/G]TGATATTTTGATAAA | 55130 |
| rs753646198 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27946766 | CCTTCTTATGACACA[C/T]GTACACATATGCAAA | 55130 |
| rs753678922 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27866118 | ACTTCTATGCATTAG[C/G]ATGCTCTCAAATCAA | 55130 |
| rs753689063 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27826253 | GACTCTCTGTTCTCT[A/C]TCATTCTTCTCCTAT | 55130 |
| rs753697246 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27959603 | AGCATGTGGCCTGAA[C/T]CTAGCCCGTGCTCCA | 55130 |
| rs753706272 | snp | A/C | 1.65562e-05 | 0.00287712 | missense | ARMC4 | GRCh38.p7 | 10:27995129 | TGCGTCAATTTCCTC[A/C]GAGCCACACCCATGG | 55130 |
| rs753721594 | in-del | -/TT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27973761 | ATGTGTGCATGTGTC[-/TT]TTTATGCGATGATTT | 55130 |
| rs753749782 | snp | C/T | 8.55234e-05 | 0.00653869 | intron-variant | ARMC4 | GRCh38.p7 | 10:27961742 | AACAACACACATACA[C/T]ATGTAAGCTATAGTG | 55130 |
| rs753755558 | snp | G/T | 7.67902e-05 | 0.0061959 | missense | ARMC4 | GRCh38.p7 | 10:27985207 | TACTATGGGGTCTCT[G/T]TTAGCTGCCAAAAAA | 55130 |
| rs753777381 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27889442 | CACAGATATAATCAT[C/T]GTAAGTGATTCTCTC | 55130 |
| rs753807004 | snp | A/G | 0.000298552 | 0.0122142 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27968972 | GTCTTGGTTTTTCAA[A/G]TTTTCCTGTGTGTTT | 55130 |
| rs753858595 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27933914 | GATACGTGGTTAGAC[A/G]AAGCCCCCTGATAGG | 55130 |
| rs753869291 | in-del | -/A/AA | 0.000343525 | 0.0131013 | intron-variant | ARMC4 | GRCh38.p7 | 10:27985215 | GTCTCTGTTAGCTGC[-/A/AA]CAAAAAAAAAAAAAA | 55130 |
| rs753874273 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27957223 | GAAAAGGAAGAGAGA[A/G]GGATGCAAGAAAAGT | 55130 |
| rs753884985 | snp | C/T | 1.71985e-05 | 0.0029324 | intron-variant | ARMC4 | GRCh38.p7 | 10:27860878 | GAAATGGGATCTGTG[C/T]ATTGTAATGACCCTG | 55130 |
| rs753896886 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27820955 | CCGGCTAATTTTGCA[C/T]TTTTAGTAGAGACAG | 55130 |
| rs753919190 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27821214 | TTTTCTGTGTGCTCC[A/G]GGTATGAATATTTGA | 55130 |
| rs753919383 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27973887 | ATGATTGAACTAATT[C/T]ACACCCACCAACAGT | 55130 |
| rs753936142 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27887582 | CATATATGAAGCCGC[A/T]AAACAAGTCTTTAAA | 55130 |
| rs753955237 | in-del | -/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27848964 | TAGTGGGACTGTAAA[-/C]TAGTTCAACCATTGT | 55130 |
| rs753957696 | in-del | -/AT | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27982165 | CTTCCATAACAGAAT[-/AT]ATATATATATAATGT | 55130 |
| rs753958229 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27861025 | TAGATGGAGTCTCAC[C/T]CTGTTGCCCAGGCTG | 55130 |
| rs753960548 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27988905 | CTATTCTGGGTATTT[A/G]GAGGAAGCCAAACAT | 55130 |
| rs753983228 | snp | A/C/T | 4.84945e-05 | 0.00492396 | missense, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27985089 | GCATAGCAATCTTCA[A/C/T]CTTAATTTCACTTTC | 55130 |
| rs754032181 | in-del | -/AAAAAAAAAAAA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27943796 | GTGAGGCTCTGTCTC[-/AAAAAAAAAAAA]AAAAAAAAAAAAAAA | 55130 |
| rs754032308 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27860560 | GAAATCTTAGTGATG[C/T]CTAAGTTTCTTTCCA | 55130 |
| rs754043604 | in-del | -/TA | 3.50557e-05 | 0.00418648 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944477 | ATATGTAACCCGTGC[-/TA]TGTTTTTAAAAATTC | 55130 |
| rs754071683 | snp | A/G | 2.1883e-05 | 0.00330772 | missense, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27985029 | CTCACAATGAAATAT[A/G]TTTTAGAGAATGATT | 55130 |
| rs754085138 | snp | A/G | 1.67195e-05 | 0.00289127 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944446 | TCTGTGTGAGAAAAA[A/G]AAAGATGAGTGGCGA | 55130 |
| rs754092688 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27910643 | ACGACTCTAATCTCA[C/G]CTACTTGGGAGGCTG | 55130 |
| rs754142424 | in-del | -/T | | | frameshift-variant | ARMC4 | GRCh38.p7 | 10:27860734 | TCATTTGATTTCAGA[-/T]AACGCACTAGTGGAG | 55130 |
| rs754157507 | snp | A/G | 1.64798e-05 | 0.00287047 | synonymous-codon, missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27812542 | CTTCTCTGTAGCAAG[A/G]GCCAGCCTGCGGATA | 55130 |
| rs754183341 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27982385 | GCTAAATAAGTTATA[C/T]GTATGTAGATCAATA | 55130 |
| rs754213558 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27987857 | TTTCTAAAATGTGTT[A/G]ATTTCTGGCATCTTT | 55130 |
| rs754214367 | snp | A/G | 1.65192e-05 | 0.00287391 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27812603 | AGATCCTGGTCAGGG[A/G]ACCCAACCATATCCA | 55130 |
| rs754215845 | snp | G/T | 1.65315e-05 | 0.00287498 | stop-gained, utr-variant-5-prime, intron-variant | ARMC4 | GRCh38.p7 | 10:27981536 | AGGTTTTTATAAATT[G/T]AACCTTTTCTCTCAT | 55130 |
| rs754225187 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27816023 | ACTTAGTTGTTCAAG[A/G]CGGAAATCTGCGTGC | 55130 |
| rs754237024 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27886903 | AAAGGATATCAAAAT[A/G]TGTCACTATAAAAAG | 55130 |
| rs754237369 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27829358 | GAAAGATTCTTTTGG[C/T]CCAGTAATTGCTTTT | 55130 |
| rs754257435 | in-del | -/TT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27911804 | TGTGTTGTGTGCTTC[-/TT]ATCTCCCCAATTACC | 55130 |
| rs754269401 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983428 | ATAGGGCACTGTCTC[C/T]TACCTTCTACATTTA | 55130 |
| rs754307598 | snp | A/G | 1.64991e-05 | 0.00287215 | missense | ARMC4 | GRCh38.p7 | 10:27994968 | CCAAACTTGTGTTCC[A/G]TTCAAGTGGTTCCAC | 55130 |
| rs754312546 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27903564 | CCATCGTCTCAGCCG[-/A]AAAATCTCCTTAAGC | 55130 |
| rs754318548 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27857331 | AATACATATAACATA[C/G]GAAATATGTATTAAT | 55130 |
| rs754323497 | snp | C/T | 5.88957e-05 | 0.00542627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27994881 | TAATACTATGTACAA[C/T]GAAGATATCAAATCC | 55130 |
| rs754326827 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27938146 | GTTTCACCACGTTGG[C/T]CAGGCTGGTCTCGAA | 55130 |
| rs754339970 | in-del | -/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27985272 | CTTCTAGTACAACAA[-/G]ACATTAAGACTAATA | 55130 |
| rs754342225 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27950931 | TTCAATAAAGTGGAC[A/G]CAAGAGCAGCATTTT | 55130 |
| rs754354270 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27952437 | ATACATGTGCAGAAC[A/G]TGCAGGTTTGTTACA | 55130 |
| rs754364124 | snp | A/C | 1.64827e-05 | 0.00287073 | missense | ARMC4 | GRCh38.p7 | 10:27940699 | TGACTCTTACTGCAG[A/C]TCCACAGGGCCAGTG | 55130 |
| rs754371287 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27904243 | CCTTCCAGACTTTCT[A/G]TAAGAAGTGTGGCAA | 55130 |
| rs754376700 | snp | C/T | 3.33734e-05 | 0.0040848 | intron-variant | ARMC4 | GRCh38.p7 | 10:27971358 | ATGATATCTGAATTA[C/T]CTAGTGTTCTCTGAA | 55130 |
| rs754422430 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27917160 | AAGCCTAATATGAAA[G/T]AACTGAAATCACATA | 55130 |
| rs754430919 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27919148 | AAATAGACCCATTCA[C/T]TTACAATCAGTTGAA | 55130 |
| rs754453943 | snp | A/G | 1.64882e-05 | 0.00287121 | intron-variant | ARMC4 | GRCh38.p7 | 10:27981416 | ACCATAGAAAGTTGT[A/G]GTTTAGTAACATAAT | 55130 |
| rs754457750 | snp | A/G | 1.64879e-05 | 0.00287118 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27995008 | TTTTGCCTCTTGAGG[A/G]TGTTTATAGATAAAA | 55130 |
| rs754472947 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27948676 | GGGCTTTGAAAAATG[C/T]TTCCAATAAGTGTTT | 55130 |
| rs754487896 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27851524 | GAGATCCAAATGAAA[C/T]GTCGATAGTATTGCA | 55130 |
| rs754489256 | snp | G/T | 1.64841e-05 | 0.00287085 | missense | ARMC4 | GRCh38.p7 | 10:27935046 | GCACAAGCACCAACT[G/T]CTTTTGTAACATTCA | 55130 |
| rs754499260 | snp | A/G | 3.33868e-05 | 0.00408562 | intron-variant | ARMC4 | GRCh38.p7 | 10:27907800 | GGAACCCAAAATCAT[A/G]ATATAAACTGTCATT | 55130 |
| rs754506887 | snp | A/G | 0.000132068 | 0.00812505 | synonymous-codon, utr-variant-5-prime, intron-variant | ARMC4 | GRCh38.p7 | 10:27981559 | TCTCTCATAATTAAC[A/G]TCCCCTTCATCATCT | 55130 |
| rs754510767 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27963621 | CTTAACTTGTTGCTA[A/C]GGCCTTATATGAACC | 55130 |
| rs754515966 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27814679 | ACATACTTTTCCTTT[A/T]ACCATCTTCCGTCTT | 55130 |
| rs754527947 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27878773 | AATACAGCCTATATA[C/T]CCTCAAGCACAGAGA | 55130 |
| rs754541539 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27944467 | TGAGTGGCGAATATG[C/T]AACCCGTGCTATGTT | 55130 |
| rs754562177 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27852513 | ACTCTAAAGCAATCA[C/T]TAAATGACAACACGG | 55130 |
| rs754588720 | snp | C/T | | | downstream-variant-500B, intron-variant | ARMC4 | GRCh38.p7 | 10:27811949 | ATGTTTGCTAGTATT[C/T]AGGAGAAATTTGGGA | 55130 |
| rs754609145 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27972601 | AGTTTATGCAAACAA[C/T]AATCAAAAGAAAGCA | 55130 |
| rs754610842 | snp | G/T | 1.64825e-05 | 0.00287071 | missense | ARMC4 | GRCh38.p7 | 10:27940726 | AGTGCCCCACAGCGA[G/T]CCACTTCCACGTCTC | 55130 |
| rs754615918 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27877051 | AGTGAACATTCAAAA[A/G]TATTTGTTGAATTGT | 55130 |
| rs754666804 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27890853 | CAGATGGGTGCATAC[G/T]TAGAACTATTTGGTG | 55130 |
| rs754695884 | snp | C/G | 2.31062e-05 | 0.0033989 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984995 | GCTCAATACAATAGA[C/G]GTTCCTTTTTGAAAA | 55130 |
| rs754705513 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27877678 | ACGACTGGGCAAATT[A/C]ACCACATTTTCCACC | 55130 |
| rs754726550 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27957400 | CGAGCCTGTGCACAC[C/T]AGCAAGATGCCCTGC | 55130 |
| rs754816998 | snp | C/T | 1.69838e-05 | 0.00291404 | intron-variant | ARMC4 | GRCh38.p7 | 10:27961527 | TTTGGGAAAGTATTT[C/T]AAATGAACATTGCAA | 55130 |
| rs754825267 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27923907 | TAAGCTATGATTACA[C/T]CACTGCATTCCAGGT | 55130 |
| rs754840032 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27821523 | CTTTAAACTAAGGCA[C/T]TAGTTTCTTTAAAAC | 55130 |
| rs754841451 | snp | A/G | 1.64743e-05 | 0.00287 | missense, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27961639 | TTGCTTCCTGACGAT[A/G]GTCAGGTGGTTCTTC | 55130 |
| rs754855981 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27836395 | TCCCTGCATCCTGTC[-/T]TTTTTTACGTCATTA | 55130 |
| rs754871301 | snp | C/T | 1.64768e-05 | 0.00287021 | missense, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27936748 | CATTCTCTTTGCTGA[C/T]GGAACATTTCCATAT | 55130 |
| rs754888898 | snp | C/T | 1.64887e-05 | 0.00287125 | missense, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984261 | AGTTCTATATCCTTC[C/T]TCACCGTCATGGGAC | 55130 |
| rs754896331 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27861272 | GCTGAGATTACAGGC[A/G]TGAGCCACTGCACCC | 55130 |
| rs754896400 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27822718 | CTGGCTGGAGCAAAA[C/T]CTTTGGTTCTATTTG | 55130 |
| rs754917958 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27923303 | CTAAAAAAGTGTAGA[A/T]CAAGATATATCAAGC | 55130 |
| rs754923153 | snp | G/T | 1.64817e-05 | 0.00287064 | missense | ARMC4 | GRCh38.p7 | 10:27860760 | TGGAGCCACTGCTTT[G/T]TGCTCACCGAAGGCC | 55130 |
| rs754949069 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27834383 | CCCGTGACACCACAG[A/G]CATCCCTTACATAGG | 55130 |
| rs754950817 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27863405 | CAGAGAATCGCCTTC[C/T]TCAGCCTCAGCTGAG | 55130 |
| rs754956645 | in-del | -/AAAAAAAAAAAA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27943798 | GAGGCTCTGTCTCAA[-/AAAAAAAAAAAA]AAAAAAAAAAAAAAA | 55130 |
| rs755007652 | snp | C/T | 5.04096e-05 | 0.00502018 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27944259 | TGCCTCACCACCCGC[C/T]GTGCTCTTTTAAACT | 55130 |
| rs755020971 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27869811 | AAGAGCTAGGATTAC[A/G]GGCATGAGCCACCAT | 55130 |
| rs755027513 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27920976 | TGTGTATGTGAAAGA[A/G]TCTTTCATTACACGA | 55130 |
| rs755032901 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27910850 | TCAGTGCAAACCTTT[C/G]ATGAACAAATAGTGA | 55130 |
| rs755044554 | snp | C/G | 1.65277e-05 | 0.00287464 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984007 | ATCAAGCAATTAACA[C/G]GAGTTCCTTAACCTA | 55130 |
| rs755049286 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27973909 | ACCAACAGTGTGTAC[A/G]TATTCCCTTTTTTTC | 55130 |
| rs755087063 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27986399 | ATGGATAAGTATTCA[A/G]CTATATAGAAATCTA | 55130 |
| rs755095707 | snp | G/T | 1.64974e-05 | 0.00287201 | missense, intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27971229 | AACCAGAAATGTCTT[G/T]GCGGAGGGCAGCTGC | 55130 |
| rs755099287 | snp | A/G | 1.66394e-05 | 0.00288434 | intron-variant | ARMC4 | GRCh38.p7 | 10:27935275 | CATCATAAGAAAGAG[A/G]AGAATTGGTTTTTGT | 55130 |
| rs755101661 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27954355 | GGCAAGAAATTCCCC[A/G]AAAAGATCTACTACA | 55130 |
| rs755114085 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27994618 | GGTGGAAAGGCCAGG[A/C]ATAAAGCAGCAATGG | 55130 |
| rs755116769 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27933889 | AGGAGGTGTTAGTAC[C/T]TGTGTATAAGATACG | 55130 |
| rs755127066 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27832762 | TTTCAGCAGGATACA[A/C]TCACAATGGGTATCC | 55130 |
| rs755170204 | snp | C/G | 2.61032e-05 | 0.0036126 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944209 | TGACGATGACAACAT[C/G]ACGGCTACTCACCAG | 55130 |
| rs755187743 | in-del | -/TGTTGTGTTCAACACAAATCA | 1.64806e-05 | 0.00287054 | cds-indel, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27944946 | ACGCAATCACTGTAG[-/TGTTGTGTTCAACACAAATCA]CTGTTTGATTTCCTC | 55130 |
| rs755213829 | in-del | -/AAAT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27970101 | AGATTCTGTCTCAAA[-/AAAT]AAATAAATAAATAAA | 55130 |
| rs755263004 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27881529 | GTAGTCCCACTTACT[C/T]GGGAGGCTGAGGTGA | 55130 |
| rs755266870 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27932079 | AGCTAGGACTACAGG[C/T]GCACACCCTCACATC | 55130 |
| rs755277921 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27818574 | TAGAGGACCTAATCC[C/T]ATACTAAGAGCTTGA | 55130 |
| rs755282563 | in-del | -/CACTTCT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27906212 | AAAGATATGAAAAGA[-/CACTTCT]CACTTCTCAAAAGAA | 55130 |
| rs755285563 | snp | A/C/T | 1.65111e-05 | 0.0028732 | missense, stop-gained | ARMC4 | GRCh38.p7 | 10:27862547 | CACTTGCCAGAACTT[A/C/T]TTTGTTATCTGATTT | 55130 |
| rs755324201 | snp | C/T | 1.72991e-05 | 0.00294096 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940031 | AAAAACCTACATATT[C/T]ATGTGTTCAAGACGT | 55130 |
| rs755328209 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27980973 | TGTGGTCTATACATA[A/C]ACAAAATATTATTCT | 55130 |
| rs755333740 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27896847 | TAAACCTGAGCTATC[A/T]TCTGGATTTCATACT | 55130 |
| rs755352502 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27907278 | CTCTCACTGCAGGCT[A/G]TAAGGACAATAGAAG | 55130 |
| rs755356845 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27956481 | GGCAGATATCCAACT[A/G]TGCTTGCCAATATAA | 55130 |
| rs755359952 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27942121 | ATGCAGTATGGAAGT[A/G]CTCAGAAAGCCCGTA | 55130 |
| rs755365932 | snp | C/G | 1.69637e-05 | 0.00291231 | intron-variant | ARMC4 | GRCh38.p7 | 10:27987340 | CCACTTTCCCAGCAA[C/G]ATTGTTTCTAAAAGT | 55130 |
| rs755383082 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27979538 | TCAAAAATTAGATCT[C/G]ATTTGATCACTCAAA | 55130 |
| rs755413599 | snp | A/G | 1.71758e-05 | 0.00293046 | intron-variant | ARMC4 | GRCh38.p7 | 10:27862631 | CAGCATCCTAGACAA[A/G]AATAAAAGTAAAGAT | 55130 |
| rs755427212 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27941076 | AACATGGCTCTAATA[C/T]TTACATCAATCATAT | 55130 |
| rs755452097 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27813666 | ACTAAGAAAAATATC[A/G]TGAGATGTCTTACAT | 55130 |
| rs755504651 | in-del | -/TAATT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27985274 | TCTAGTACAACAAAC[-/TAATT]ATTAAGACTAATAAA | 55130 |
| rs755507630 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27826744 | TAACCCCCCTCTTTC[C/T]GGTATTTTCACTGCC | 55130 |
| rs755511655 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27841352 | ACAGCTCACCAGCCT[C/T]GTAGACAGATCAGCT | 55130 |
| rs755525961 | in-del | -/AC | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27903646 | CATAAGCATTCCTAT[-/AC]ACCAATAATAGACAA | 55130 |
| rs755540377 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27865132 | TTTCAAGGTGCACCC[C/T]TGGTTTATCTCTCCA | 55130 |
| rs755541892 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27892382 | TAAAAAAGACCGTGC[A/G]GCTTTCTAAGTGAAG | 55130 |
| rs755559344 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27882931 | GCAATTATTTAACAA[A/C]AAAAAAAGCTGCTTG | 55130 |
| rs755589164 | snp | C/T | 3.31972e-05 | 0.004074 | synonymous-codon, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983864 | TAAAAATACTCCTCC[C/T]GCACTGCAAGTAATG | 55130 |
| rs755589354 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27938025 | CTCAGATCACTGCAA[A/C]CTCTACCTCGTGGGT | 55130 |
| rs755590966 | snp | A/G/T | 0.00011972 | 0.00773614 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944466 | ATGAGTGGCGAATAT[A/G/T]TAACCCGTGCTATGT | 55130 |
| rs755596933 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27903624 | TACAAAATCAATGTG[C/T]AAAAGTCATAAGCAT | 55130 |
| rs755619175 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27961503 | AAACTTGGAAGCAGC[A/T]TATACATCTTTGGGA | 55130 |
| rs755625187 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27989719 | CCAGGCATGGTGGCA[C/T]GTGCTTTGGTCCCAG | 55130 |
| rs755640068 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27950928 | TAGTTCAATAAAGTG[A/G]ACACAAGAGCAGCAT | 55130 |
| rs755642842 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27991558 | TGTGCAACATCAAAT[A/G]AGAACTAAAGCCACA | 55130 |
| rs755707180 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27994888 | ATGTACAACGAAGAT[A/T]TCAAATCCTAGAAGC | 55130 |
| rs755711506 | snp | C/T | | | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27959004 | AATGGACCGGGACTC[C/T]TGGGAAAAACTCAGG | 55130 |
| rs755722732 | in-del | -/AG | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27945466 | CGTGGGATTGGGAAA[-/AG]AGAGGCAATTCCAGC | 55130 |
| rs755735828 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27854920 | AAACAAAAAAACCAA[A/G]TACTTACTGTAGGAA | 55130 |
| rs755735993 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27835565 | TTTTGACTGCCCCCA[A/G]TCTTAAGGACTGATA | 55130 |
| rs755755936 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27833888 | GAGCAAATCTGAAAC[C/T]TGAAAGATGGTTATG | 55130 |
| rs755758660 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27879282 | CTTACAGAGTTAATT[A/G]CATGACATTCTTAAC | 55130 |
| rs755760697 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27861355 | TGAGTTTTCTTCTTA[C/T]GAACTGAATGTAGTC | 55130 |
| rs755772185 | in-del | -/TA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27940383 | ATATACATATATGTG[-/TA]TATATATATCACAGG | 55130 |
| rs755782937 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27976780 | CATGCAAAAGATCTA[C/G]AATAGCCAAAAAACT | 55130 |
| rs755790914 | snp | A/T | 1.64838e-05 | 0.00287083 | missense | ARMC4 | GRCh38.p7 | 10:27935072 | ATTCACAAGAAGAGC[A/T]TGGTTTATTCCAACA | 55130 |
| rs755800797 | in-del | -/AA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27977400 | AACCCCATTTCTGCT[-/AA]AAAAAAAAAAAAAAA | 55130 |
| rs755819240 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27911723 | CATCTTCCTCCTTTA[A/C]GCTTCTTTTTAATTT | 55130 |
| rs755820365 | snp | C/T | 1.65135e-05 | 0.00287341 | intron-variant | ARMC4 | GRCh38.p7 | 10:27981610 | ACAAGTTTCATTCTA[C/T]GATTAACATAAGAAC | 55130 |
| rs755843584 | snp | A/C | | | utr-variant-3-prime, intron-variant | ARMC4 | GRCh38.p7 | 10:27812368 | CAGATGAAAAACATT[A/C]TGTGCATTTTCAATT | 55130 |
| rs755845738 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27862119 | TCGAGAATCATAACC[A/G]TGATGGTGGCGGTGA | 55130 |
| rs755846295 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27993658 | CTGTCTCCAGAAAAA[A/T]AAATAAATAAATAAA | 55130 |
| rs755848005 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27893137 | GCCCTCCAACCTGGG[C/T]GACAGAGCCAGACTC | 55130 |
| rs755850184 | snp | C/T | 1.65332e-05 | 0.00287512 | missense | ARMC4 | GRCh38.p7 | 10:27995118 | CAGCAGTCCACTGCG[C/T]CAATTTCCTCAGAGC | 55130 |
| rs755852380 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27925941 | AGCCCGGGATGCAAG[G/T]GTTGCAGTGAGCCAA | 55130 |
| rs755853670 | snp | A/C | 1.70682e-05 | 0.00292127 | intron-variant | ARMC4 | GRCh38.p7 | 10:27961733 | AAGAACAATAACAAC[A/C]CACATACACATGTAA | 55130 |
| rs755862193 | snp | A/G | 9.88973e-05 | 0.00703128 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27995052 | CAATAATTTCTTTCA[A/G]TATCGCTTCATTTAG | 55130 |
| rs755863141 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27836403 | ATCCTGTCTTTTTTA[C/T]GTCATTAAATAAAAA | 55130 |
| rs755909325 | snp | C/T | 5.01802e-05 | 0.00500875 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940824 | TAATAATAGATAAAT[C/T]CAATGTTCATGGAAA | 55130 |
| rs755924541 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27899340 | GGAGATTCCCTCAGG[C/T]GCCCACACCACCAAA | 55130 |
| rs755961509 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27998613 | CCGAGGCAGGGTCTC[G/T]CGGGGAGGAAGGAGT | 55130 |
| rs756011557 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27844446 | CAACCAGGCTCAGTC[C/T]TTCAGAAAAAACTGC | 55130 |
| rs756018516 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27958453 | CCATTAAATCCTAAG[A/G]GAGAAAATTCTTTCT | 55130 |
| rs756019274 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27946607 | TTGACTGTACTACAA[C/T]AGGGAACTTGAACTT | 55130 |
| rs756021262 | snp | A/T | 0.00390522 | 0.0440154 | missense, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27961652 | ATGGTCAGGTGGTTC[A/T]TCATCTTCCTCACTT | 55130 |
| rs756027516 | snp | A/G | 1.69663e-05 | 0.00291253 | intron-variant | ARMC4 | GRCh38.p7 | 10:27860863 | TGTGCAAGGGAAAAT[A/G]AAATGGGATCTGTGC | 55130 |
| rs756040812 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27824991 | TTGGATATAAAAATG[A/G]CACCTCAAAAGGGAC | 55130 |
| rs756045699 | snp | A/G | | | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999742 | TAAGGACCAATGCCG[A/G]AGCACTTAGGATGAT | 55130 |
| rs756087698 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27907207 | AGTGACAGATAAGAA[A/T]AGTGAGAGTCATTGA | 55130 |
| rs756093940 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27966112 | TTAATTTCTTACAGG[-/T]TTTTTTGGCACAGAG | 55130 |
| rs756104153 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27905746 | ATCTTTGACAAACCT[A/G]ACAAAAACAAGCAAT | 55130 |
| rs756107542 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27888486 | TTGAAAAATGTCTAT[G/T]CATGTTCTTTGCCCT | 55130 |
| rs756131767 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27883203 | GTAGTAATATTAATG[C/T]ACACAGAACCCTTAT | 55130 |
| rs756149148 | snp | C/T | | | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999325 | ATATTCCTTAGAAAC[C/T]CCTTTTTACATTTTT | 55130 |
| rs756163906 | snp | A/G | 1.64939e-05 | 0.0028717 | synonymous-codon, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984272 | CTTCTTCACCGTCAT[A/G]GGACTTAAACTTATT | 55130 |
| rs756164610 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27900098 | AGGTGCCCCTCTAGG[A/C]CAAAGCTTCCAGAGG | 55130 |
| rs756210234 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27941324 | TCCTGTTTCCACTGG[A/G]AAAAAAAAAAAAAAG | 55130 |
| rs756218312 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27922242 | TTATATCTAGCAAGG[C/G]TGTCCACTGAGTATT | 55130 |
| rs756227566 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27814730 | TAGATTGCATAGTCC[A/G]TCTTTTGAATCATTC | 55130 |
| rs756229290 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27972192 | GTTTCTTAAACTATT[C/T]GTGAATTTTAGAATT | 55130 |
| rs756233009 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27942176 | CATGGTGGTTAGCAG[G/T]TGCTCCTCACAATCT | 55130 |
| rs756249650 | in-del | -/TGTTTCA | 1.64827e-05 | 0.00287073 | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27936676 | TAAATGACAAGAAGG[-/TGTTTCA]GAAGCCGTATCTTCA | 55130 |
| rs756265006 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27954583 | TTGTCATGTTTCAGT[C/T]GTTAAGTTGATGTGG | 55130 |
| rs756274935 | in-del | -/AAAC | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27859837 | CTGATGCACAGATTT[-/AAAC]AAACAAACAAACAAA | 55130 |
| rs756295807 | snp | C/T | 1.66815e-05 | 0.00288799 | intron-variant | ARMC4 | GRCh38.p7 | 10:27935284 | AAAGAGGAGAATTGG[C/T]TTTTGTATAAGGTTT | 55130 |
| rs756334233 | snp | C/G/T | 3.29855e-05 | 0.00406102 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27944352 | ATATTCACCATAATT[C/G/T]GTAAGCCCCCAAGGT | 55130 |
| rs756363569 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27840269 | ACCTCATAATAAAAG[A/C]ATATATTTGACTCTA | 55130 |
| rs756377346 | in-del | -/AAAAAA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27852963 | AGACACAGTCTCAAA[-/AAAAAA]AAAAAAAAAAAAAAA | 55130 |
| rs756401498 | in-del | -/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27858265 | CAGGTTGTTATGCTT[-/C]CCCCCATGACCCCAC | 55130 |
| rs756407657 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27995598 | CAGCCAGGACACACA[C/T]TGTTTAGAATTACAC | 55130 |
| rs756423734 | in-del | -/C | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984999 | AATACAATAGAGGTT[-/C]CTTTTTGAAAAAGAC | 55130 |
| rs756449029 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27895251 | TGCATATCTCAGACC[A/T]GGGCACCAAAACGAT | 55130 |
| rs756478760 | snp | A/G | | | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27981861 | GGCACTCTGCTGTTC[A/G]GCAGAGAAGTGAGAG | 55130 |
| rs756544311 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27949969 | CATTTGAAGTTATTA[C/T]CAGAGCCCCACATGA | 55130 |
| rs756545712 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27868054 | CTCAAAAGAAGACAT[C/T]TATGCGGCCAACAAA | 55130 |
| rs756548463 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27815912 | AGTCTCACAGCCACC[C/T]CAAGCTTAATAGATT | 55130 |
| rs756567170 | snp | A/T | 2.86299e-05 | 0.0037834 | intron-variant | ARMC4 | GRCh38.p7 | 10:27971344 | GAGAATAATTTTTAA[A/T]GATATCTGAATTATC | 55130 |
| rs756576898 | snp | A/T | 2.0418e-05 | 0.00319508 | intron-variant | ARMC4 | GRCh38.p7 | 10:27862658 | AGATGGTATCAAAAC[A/T]AAACCTACATTTAGG | 55130 |
| rs756606835 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27854601 | TCTCTACCAAAAATA[C/T]AAAAATTAGCCCGGT | 55130 |
| rs756624052 | snp | A/G | 6.61759e-05 | 0.00575183 | missense | ARMC4 | GRCh38.p7 | 10:27907680 | TTGCATTTTTGATGC[A/G]TGGACAGAGTGCCCA | 55130 |
| rs756637693 | snp | C/T | 1.65015e-05 | 0.00287237 | missense | ARMC4 | GRCh38.p7 | 10:27987454 | AAGCGTGACAGCTGC[C/T]CAAAGCTCCTAATTT | 55130 |
| rs756655378 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27880182 | GACTCCCCTGTCCTG[A/C]CCTTACAGGATTTCT | 55130 |
| rs756663024 | in-del | -/TAGA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27969090 | TAAAAGATGGCAATG[-/TAGA]TAGATATATACTCCG | 55130 |
| rs756674450 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27825882 | GAGCTACTGAATCTG[C/T]TTTTCTAATATATGA | 55130 |
| rs756713541 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27902256 | AAGTTCTTTGAAATC[A/G]ATGAGAACAATGACA | 55130 |
| rs756734006 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27927914 | ATATATCCATGACAT[A/C]AGTTACCAAATATTC | 55130 |
| rs756738910 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27914318 | CATTTTAAAGATGCC[A/G]TTTTTTCTTTTCATT | 55130 |
| rs756742569 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27898184 | ATGACCATTGACAGT[C/T]AATCAGTATCTATAA | 55130 |
| rs756749089 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27917393 | TAAAGAAAAATGTAT[A/G]CCTTTAAAAAATTAT | 55130 |
| rs756768231 | snp | C/G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27977006 | CAATAGATTTACTTT[C/G/T]GACAAATGATGCTGG | 55130 |
| rs756783412 | snp | A/G | 4.9436e-05 | 0.00497148 | missense, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27944934 | CTCATTGAACACAAC[A/G]CAATCACTGTAGCTG | 55130 |
| rs756789429 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27978926 | ATTAAGATCAGGAGT[C/T]AGGCTAGGCATGGGG | 55130 |
| rs756801205 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27833318 | ATTAGCACCCGGCAA[C/T]AGTCGTACTTCGCAA | 55130 |
| rs756813598 | snp | C/T | 3.54183e-05 | 0.00420807 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940044 | TTTATGTGTTCAAGA[C/T]GTGAATATAAGTAAC | 55130 |
| rs756830869 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27985769 | GGAAAGCACATCTAG[A/C]CATATACATAATATA | 55130 |
| rs756833107 | in-del | -/ATAA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27940247 | ATGTGTGATATATAT[-/ATAA]ATGTCAGTATATGTG | 55130 |
| rs756880463 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27862157 | AGTTAACACTTACAT[A/G]ATAGCACTTGTATTT | 55130 |
| rs756900041 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27863706 | TCAACTAATATAAAG[C/G]TTCAAGGGCTGACTC | 55130 |
| rs756952164 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27883027 | GTGAGAAGTGTGTAC[A/G]GAGATTTGAAAAACA | 55130 |
| rs756953105 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27881150 | AAGCATACAGCAAGA[C/T]GTCTGGTATATGATA | 55130 |
| rs756966675 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27912006 | ACTTGCAAAATACAC[A/G]TTCAAATTCTAAATC | 55130 |
| rs756994484 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27825211 | AGAATCTGTCCTGAC[A/G]TCTTCCCATTACCAT | 55130 |
| rs757029838 | snp | A/T | 1.6549e-05 | 0.0028765 | missense, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983878 | CTGCACTGCAAGTAA[A/T]GCACAGAGTCTCACC | 55130 |
| rs757039976 | snp | A/C | 1.64912e-05 | 0.00287147 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27935183 | GGCCCCAACCACATT[A/C]ACAAGTACTTCTTCA | 55130 |
| rs757057849 | snp | A/G | 9.8894e-05 | 0.00703116 | missense | ARMC4 | GRCh38.p7 | 10:27935097 | CCAACAAGGAGGTTC[A/G]CAAGTGGTTGAATGC | 55130 |
| rs757068936 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27965966 | TTCTTTGTTTCTCTC[C/T]CTCCTCTGCTCTCTT | 55130 |
| rs757084845 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27818599 | GCTTGATTTCCATAC[A/G]CAAATGAGATTTAGA | 55130 |
| rs757096123 | snp | A/C | 8.28219e-05 | 0.0064346 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27995131 | CGTCAATTTCCTCAG[A/C]GCCACACCCATGGGA | 55130 |
| rs757132234 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27833848 | TACAGACAGCAAGGT[A/G]AAGGTACACCTCCCT | 55130 |
| rs757155470 | snp | A/G | 3.50625e-05 | 0.00418689 | intron-variant | ARMC4 | GRCh38.p7 | 10:27812673 | AAGAATAAAAACATT[A/G]ATCTAAAGACATAAA | 55130 |
| rs757155884 | snp | A/C/G | 5.0649e-05 | 0.00503213 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940841 | AATGTTCATGGAAAT[A/C/G]TTAAAAAGAACATTT | 55130 |
| rs757185842 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27813475 | ATCTAATGCATAGAA[C/G]ACAAACAAATGAATT | 55130 |
| rs757193603 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27986514 | AGACTTGATACCCTC[A/G]CCTAATAAGGAGTAA | 55130 |
| rs757194566 | in-del | -/T/TTTT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27974689 | TTCGGTCTGTTTTTG[-/T/TTTT]TTTTTTTTTTTTTTG | 55130 |
| rs757228302 | in-del | -/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27874178 | AGACTAGGATTGCAA[-/C]CCCTGCCTTTTTTGT | 55130 |
| rs757288457 | in-del | -/AAA | 0.0121187 | 0.0768928 | intron-variant | ARMC4 | GRCh38.p7 | 10:27985217 | TCTCTGTTAGCTGCC[-/AAA]AAAAAAAAAAAGGAG | 55130 |
| rs757297999 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27943581 | TACCTGAGCTCAGGA[A/G]TTCAAGACCAGCCTG | 55130 |
| rs757319222 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27856387 | TTTAAACACAAACCC[-/T]TTTGAAACTTGCTCT | 55130 |
| rs757325706 | in-del | -/AGG | 1.675e-05 | 0.00289391 | intron-variant | ARMC4 | GRCh38.p7 | 10:27812638 | AAGCTGTCACACATA[-/AGG]AGGAGAAGAAGGGAC | 55130 |
| rs757349452 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27942351 | CAATTTTTAATGTTG[A/G]AAGTGTTGGGGTCTT | 55130 |
| rs757351053 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27957268 | CAGCAGAAGGAAAGA[C/T]AGGCTCAGAGGCAGG | 55130 |
| rs757352783 | snp | C/T | 3.41986e-05 | 0.00413499 | intron-variant | ARMC4 | GRCh38.p7 | 10:27961744 | CAACACACATACACA[C/T]GTAAGCTATAGTGTG | 55130 |
| rs757368578 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27909010 | GAGAAAACAGTTTTA[C/T]TTCTCAATTAATGGA | 55130 |
| rs757379285 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27869113 | AAAGATATCTATAAA[G/T]AATTAGATATAAAAT | 55130 |
| rs757380104 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27963839 | GGCCACAAGAGTTCC[A/G]GACAACAGACTGTGG | 55130 |
| rs757402636 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27952847 | TATTTGCTTTCTGTA[A/G]GGAGCTATGAAACTT | 55130 |
| rs757404823 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27829464 | GTGTATCTTCAGAGT[C/G]TGTCTTGTCATTTGC | 55130 |
| rs757456095 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27981612 | AAGTTTCATTCTATG[A/G]TTAACATAAGAACAA | 55130 |
| rs757462822 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27886973 | AGGAATAAAAGGCTA[C/T]AAAACATACAGAAAA | 55130 |
| rs757463063 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27867289 | AGCAGAAGCAGCTGC[A/G]AATGGACTTTTCAGG | 55130 |
| rs757468929 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27867155 | GACCCCAAAGCACAA[A/G]CAGACTTGGAGGGAC | 55130 |
| rs757470055 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27899103 | CTGCATTTCCAATTG[A/G]GGTACCCATCTCATC | 55130 |
| rs757473859 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997576 | AAATTTTGACAGAAA[C/T]GTAACATTTGAATCT | 55130 |
| rs757477884 | snp | C/T | 1.64942e-05 | 0.00287173 | missense | ARMC4 | GRCh38.p7 | 10:27862501 | GCTAAATTTTCTTGA[C/T]CTTTTGCTATGTTGG | 55130 |
| rs757483308 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27892866 | AGAAAAGATGTACTA[C/T]GGCCGGGTGTGGTAA | 55130 |
| rs757508310 | snp | A/C | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983565 | GAAGCTGTGTAATGA[A/C]TCAGTGAAGTGATTA | 55130 |
| rs757516095 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27884433 | TTTGCACTTTCTCCA[C/G]CCCTTCTCTGGCACA | 55130 |
| rs757531185 | snp | C/T | 2.17697e-05 | 0.00329914 | synonymous-codon, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27985033 | CAATGAAATATGTTT[C/T]AGAGAATGATTGAGG | 55130 |
| rs757531631 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27927450 | AGATGCAGTAGGTCC[C/T]ATAAATCTAGCAATA | 55130 |
| rs757532556 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27828423 | ATGAGATCACCATTA[C/T]GGAGGATGGGAAAGG | 55130 |
| rs757553950 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27843071 | TAAAGAATGTCTGTG[A/G]TTACATTTAAGGCCA | 55130 |
| rs757559849 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27982453 | CCAGAAGGTCAAAGA[A/G]AATCATTCCTTCTTT | 55130 |
| rs757589032 | in-del | -/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27966687 | ATGTGACACAGAGAA[-/C]CTTTCATTTTTATCA | 55130 |
| rs757601344 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27816035 | AAGACGGAAATCTGC[A/G]TGCCTCACACTCACT | 55130 |
| rs757601882 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27913884 | TTGTACACTGCTGGT[A/C]GGAATGCAAATTAGT | 55130 |
| rs757625420 | in-del | -/ATA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27849548 | AGAACTTAAAATATA[-/ATA]ATAATAATAATAATA | 55130 |
| rs757643701 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27903726 | AGAATAAAATACCTA[G/T]GAATAGGGCCATCTG | 55130 |
| rs757649139 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27932635 | CCATGTTGGCTACTC[A/C]TGTCTGATATGTTCA | 55130 |
| rs757650419 | snp | C/G | 4.02649e-05 | 0.00448674 | intron-variant | ARMC4 | GRCh38.p7 | 10:27971359 | TGATATCTGAATTAT[C/G]TAGTGTTCTCTGAAG | 55130 |
| rs757669080 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27991979 | AATTCTTTGGGTAAT[C/T]GAGAATATCTCTGGT | 55130 |
| rs757695157 | snp | A/G | 1.64917e-05 | 0.00287151 | synonymous-codon, intron-variant | ARMC4 | GRCh38.p7 | 10:27944356 | TCACCATAATTGGTA[A/G]GCCCCCAAGGTCAAC | 55130 |
| rs757695598 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27856547 | AAACATCTCATCCAC[A/C]CTCATTAATGGCTTA | 55130 |
| rs757700593 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27938161 | CCAGGCTGGTCTCGA[A/G]CTCCTGACCTCAGGT | 55130 |
| rs757724229 | in-del | -/T | 1.66374e-05 | 0.00288417 | frameshift-variant | ARMC4 | GRCh38.p7 | 10:27907664 | CAGTCCGTTCTTACC[-/T]TTGCATTTTTGATGC | 55130 |
| rs757741852 | snp | C/T | 4.94319e-05 | 0.00497127 | synonymous-codon, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27936770 | TTTCCATATAGCCCC[C/T]GTGACAGCAGCTAAC | 55130 |
| rs757762137 | snp | G/T | 1.64798e-05 | 0.00287047 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27812543 | TTCTCTGTAGCAAGA[G/T]CCAGCCTGCGGATAT | 55130 |
| rs757829962 | in-del | -/GAACAAACATAAGCAT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27851956 | ACATGACATACAGAG[-/GAACAAACATAAGCAT]GATAACAGATTTCCT | 55130 |
| rs757844319 | in-del | -/AAAG | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27849651 | GAAAAAAGTGGCTTT[-/AAAG]AAAGAGTCATCCTCT | 55130 |
| rs757852757 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27929084 | AAACAAGAAATTCGA[C/T]TGTGTAAAGGTGACA | 55130 |
| rs757876931 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27904295 | ACAGGACAAGAAAGG[C/T]AAGGATGCTGTGTAT | 55130 |
| rs757883413 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27826502 | TCACTCTCAAGCATA[C/T]GTCTTTGCCTCCTAC | 55130 |
| rs757902217 | snp | A/T | 1.65034e-05 | 0.00287253 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27987465 | CTGCCCAAAGCTCCT[A/T]ATTTTAATTTGTGGT | 55130 |
| rs757917694 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27882680 | CCTCTCTCCAGCTCC[A/T]CAGTAGCCTTGAAGA | 55130 |
| rs757918472 | snp | A/T | 0.000117101 | 0.00765093 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940513 | AAACAACTTTTGGAC[A/T]AAAGAAAGTCAAGTT | 55130 |
| rs757922791 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27961017 | AAATATTCTCATATA[C/T]GCTATCTGACGTGAG | 55130 |
| rs757943737 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27857283 | TCTCATAACACTTTT[C/T]TTCCTCTAGCTAATT | 55130 |
| rs757961959 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27828973 | GTCTTCCAAAATGGG[C/T]ACATTATTAGAAGAA | 55130 |
| rs757989799 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27878839 | GTTCTGTTCCCAGTT[A/G]TTAACAAATCCAACA | 55130 |
| rs758012872 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27948428 | AGCCAATTGCTATTC[C/T]TTAAATACCAGCTAT | 55130 |
| rs758020238 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27812792 | AAACAGTGTTTAATC[G/T]GATACAGGAATTCCT | 55130 |
| rs758029310 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27986656 | TGTGCCAGAAACCCA[C/T]TGGTCACATAATTCC | 55130 |
| rs758032007 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27901923 | ATTAACAAGGATATT[C/T]GGGACTTGAACTCAG | 55130 |
| rs758051770 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27889586 | GTTGAAGCTCCACAA[C/T]CTCAAAGTCTCTGCA | 55130 |
| rs758055274 | in-del | -/AT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27940173 | TGAATTAATATACAC[-/AT]ATGTGTGTTTGTGTG | 55130 |
| rs758058871 | snp | C/T | 0.000121974 | 0.00780845 | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27959003 | TAATGGACCGGGACT[C/T]TTGGGAAAAACTCAG | 55130 |
| rs758061239 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27890642 | GAGATAGGGAGGAGA[A/C]AGGAAAGTGATAGAT | 55130 |
| rs758086768 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27901346 | AAAAACCGGGACCAG[A/C]CACTGCAAAAACATA | 55130 |
| rs758124688 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27972444 | TATTAGTAGTTACAT[C/T]AAATGAAAGTGTTTA | 55130 |
| rs758128152 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27845273 | GCTGATATTCAACAT[C/T]CTTAAAGAAAAGAAT | 55130 |
| rs758140131 | snp | C/G | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27998156 | AGGCAGCCATCAGCT[C/G]TGAGATCTATGAAAT | 55130 |
| rs758143537 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27875517 | TTCATGATGGTGATG[G/T]ACAGATGGGGTTTTG | 55130 |
| rs758151554 | snp | C/T | 1.64841e-05 | 0.00287085 | missense, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27944958 | GTAGCTGTTTGATTT[C/T]CTCCCTACAAAGATG | 55130 |
| rs758178045 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27988210 | CTTTAAAAAATATTA[A/C]GATGTTTTCATGGAA | 55130 |
| rs758192226 | snp | A/G | 9.88777e-05 | 0.00703058 | missense | ARMC4 | GRCh38.p7 | 10:27860701 | AAGGCCTGAGCTGTC[A/G]CCCGATGCACGTTGG | 55130 |
| rs758195057 | snp | C/G | | | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27996339 | CTGTATTAAATCTTT[C/G]AACTATCTATTAAAT | 55130 |
| rs758232551 | in-del | -/AA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27985217 | TCTCTGTTAGCTGCC[-/AA]AAAAAAAAAAAAGGA | 55130 |
| rs758240549 | snp | C/T | 1.65236e-05 | 0.00287429 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984001 | CCAATCATCAAGCAA[C/T]TAACAGGAGTTCCTT | 55130 |
| rs758248772 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27922474 | TAATGTTTGAATGTT[A/G]TATATAACAAAACAG | 55130 |
| rs758249171 | snp | C/T | 1.648e-05 | 0.0028705 | synonymous-codon, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27936788 | GACAGCAGCTAACCG[C/T]TCTTTATTGTCAGTG | 55130 |
| rs758264763 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27956118 | AGAACAAACAAATTA[A/G]GCTACCCCTCACCAA | 55130 |
| rs758268007 | in-del | -/AGA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27864699 | GGAAAAGAATTTGTC[-/AGA]AGATCTTGGAGTCAG | 55130 |
| rs758273051 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27821275 | GCCGCTAACTAACTG[A/T]ATTGTTTTTCCCGAG | 55130 |
| rs758289540 | snp | A/G | 6.59957e-05 | 0.005744 | missense | ARMC4 | GRCh38.p7 | 10:27935211 | TCAGGCTGATCTGTT[A/G]GAAGTCCCACCAAGG | 55130 |
| rs758296836 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27839129 | ATTCCTAATTTTGGT[A/G]ACATGATGATGTTAA | 55130 |
| rs758298756 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27974130 | TTTTTAGTGGGGTTG[C/T]TTGTTTTTCTCTTGA | 55130 |
| rs758299633 | in-del | -/TGAA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27954500 | ATAAACACGAGTGAA[-/TGAA]TGAATGAATGAATGA | 55130 |
| rs758326375 | in-del | -/AT | 3.38989e-05 | 0.00411683 | intron-variant | ARMC4 | GRCh38.p7 | 10:27961545 | ATGAACATTGCAAAC[-/AT]ACTACCATAGACCTT | 55130 |
| rs758354376 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27877590 | CTCGCATAGTTTCTA[C/T]GGAAAGGGAGGCAGT | 55130 |
| rs758358922 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27835022 | CGACAGAACACACAA[C/T]CGAAGGCGCAGGGGT | 55130 |
| rs758391459 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27867019 | GAGGAATTCTGGACA[C/G]ATGATAGTGGCAAAG | 55130 |
| rs758405153 | snp | A/G | 1.66477e-05 | 0.00288506 | intron-variant | ARMC4 | GRCh38.p7 | 10:27971057 | TGTGAAAAATTAGGT[A/G]AGTATGGTTACTAAT | 55130 |
| rs758409088 | snp | A/C/T | 1.67069e-05 | 0.00289019 | intron-variant | ARMC4 | GRCh38.p7 | 10:27860583 | TCTTTCCAGGCTACA[A/C/T]TTACCAAACTTGGAC | 55130 |
| rs758451243 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27932737 | TGCTTGAGCTAAAGT[A/G]ACCAACTCCCACCCA | 55130 |
| rs758467082 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27887386 | AGGGAAAAATAGGCA[A/G]CTTCAATATCCCATT | 55130 |
| rs758480223 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27923593 | AATAAGATAGAAGAC[A/C]TAAGTAATATAAAGT | 55130 |
| rs758480324 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27890336 | TGATGCTGGGCACTC[C/T]TGGCTGAGGTGAATA | 55130 |
| rs758495408 | snp | A/G | 0.000335984 | 0.0129568 | intron-variant | ARMC4 | GRCh38.p7 | 10:27985225 | AGCTGCCAAAAAAAA[A/G]AAAAAGGAGACAAAT | 55130 |
| rs758520161 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27899275 | TGAGGAACAGTATAC[G/T]CTGGCCCAGATACTA | 55130 |
| rs758522726 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27892596 | ACATACTTGCTTTCT[C/T]CAAAATGAAGTTTTA | 55130 |
| rs758529119 | in-del | -/AAAT | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997723 | ATGTTATTAGAAAAT[-/AAAT]AAATAAATAAATAAA | 55130 |
| rs758546531 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27869622 | TCACTGCAACTTCCG[C/T]CCCCTAGGTTCAAAT | 55130 |
| rs758552927 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27844377 | CATGAAGCAAGCAAA[C/T]TCTCTGCCAAGTCCC | 55130 |
| rs758553200 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983619 | AATGGGTCACTTTGA[A/G]GCCCATTTCTTATCA | 55130 |
| rs758575388 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27948204 | CTGTAAATCATCAGC[-/T]TTTTTTTCTGAAAAT | 55130 |
| rs758600991 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27888319 | CCTCACCCTTGCCAA[A/C]ATACATTGTTTTTGT | 55130 |
| rs758617146 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27919490 | CAATCCAATTAAAAA[C/T]GGGCAAAAGACTTTA | 55130 |
| rs758628518 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27966000 | CTCCCAGTGGGTTCT[C/T]GTCCATAAAAGTCTT | 55130 |
| rs758672832 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27868486 | GATATATACACCATG[A/G]AGTATTATGCAGCCA | 55130 |
| rs758676572 | snp | A/G | 1.65608e-05 | 0.00287752 | missense, utr-variant-3-prime | ARMC4 | GRCh38.p7 | 10:27936876 | GTTTCCTTATCTTCA[A/G]CACACTGCACGAAAA | 55130 |
| rs758700863 | in-del | -/CTCCA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27976053 | AAAACACATGATTCT[-/CTCCA]CAGTACACAAAGAAA | 55130 |
| rs758701214 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27904405 | TGCTTAAGCCCAGCA[A/G]GTGGAGGTTACAGTG | 55130 |
| rs758709954 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27856910 | AGGCGGGGGTTGCAG[C/T]GAGCCGAGATTGAGC | 55130 |
| rs758724561 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27831181 | AGATAATGCTACCTC[A/G]GCCTGCAACACTGAT | 55130 |
| rs758752129 | in-del | -/GGAGTGCAGTGGTG | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27858852 | TCTATCACCCAGGCT[-/GGAGTGCAGTGGTG]TGATATCAGCTCACT | 55130 |
| rs758762130 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27939180 | CTGGCTAGTCTTGGT[A/G]GGAGATAAATGCCCC | 55130 |
| rs758764784 | snp | G/T | 1.69332e-05 | 0.0029097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944458 | AAAAAAAGATGAGTG[G/T]CGAATATGTAACCCG | 55130 |
| rs758778095 | snp | A/C | 1.65061e-05 | 0.00287277 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944796 | CAAGACTCCGCATCC[A/C]AGGTGACAGAGCCAC | 55130 |
| rs758783044 | snp | C/T | 0.000367242 | 0.0135457 | intron-variant | ARMC4 | GRCh38.p7 | 10:27812634 | GTAGAAGCTGTCACA[C/T]ATAAGGAGGAGAAGA | 55130 |
| rs758822303 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27992458 | ATTCAGGGGGCCAAG[G/T]TAGAAGGATCTCTTG | 55130 |
| rs758823185 | snp | C/T | 2.90736e-05 | 0.0038126 | missense | ARMC4 | GRCh38.p7 | 10:27985125 | CATCATCTCTGGTAA[C/T]TTTGCCAAGAATATT | 55130 |
| rs758857278 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27952542 | CTATTTGTCCTAATG[C/T]TTGCCCATCCCCTTT | 55130 |
| rs758871961 | snp | C/T | 0.000193827 | 0.00984257 | intron-variant | ARMC4 | GRCh38.p7 | 10:27860891 | TGCATTGTAATGACC[C/T]TGCAAGATCATGTCT | 55130 |
| rs758887185 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27940466 | CTGACTTCTAGAAAA[A/C]GAATGTCCTTGAGCC | 55130 |
| rs758896883 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27818419 | TTGACTCCATTGTTA[C/T]ACAAAATATAGCAGA | 55130 |
| rs758902576 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27965511 | TTCATTTGGGCTATT[A/G]CAGAGCAAGATACGG | 55130 |
| rs758930945 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27825284 | ATTAGGCCAAGTTCT[C/T]AATACGCAAAAAGAT | 55130 |
| rs758943621 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27838303 | TAACTTCTTATACGA[A/G]AACACTATTTTGGGT | 55130 |
| rs758962070 | in-del | -/AA/AG | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27924049 | AGAAAGAAGGAAAGA[-/AA/AG]GAAAGAAAGAAAGAA | 55130 |
| rs759020460 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27964513 | GGCCTGCTGGCTGCC[A/G]GGTATCAAGTGAATG | 55130 |
| rs759021852 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27895279 | GATAGCCGCTAACTA[C/T]ATGTAACTATTTATA | 55130 |
| rs759028816 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27830353 | CCCCAAACCACTGCA[C/T]CATAGTCCCTGAAGC | 55130 |
| rs759039864 | snp | A/G | 0.000855371 | 0.0206629 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27985171 | TTCTTTCATTGTATT[A/G]TAATCAGAGCCCAGG | 55130 |
| rs759047564 | snp | C/T | | | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:28000706 | ATCTGAGCAACTATG[C/T]CGTTGTTTGCCAAAT | 55130 |
| rs759061144 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27955235 | TCACATTCTTTTCCA[-/T]TTTTTTTTTTAAGTA | 55130 |
| rs759066273 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27815784 | CATCTTTCACTACCT[A/G]AATTCAAATGGCATT | 55130 |
| rs759071828 | snp | C/T | 1.65187e-05 | 0.00287386 | missense | ARMC4 | GRCh38.p7 | 10:27995114 | CCGGCAGCAGTCCAC[C/T]GCGTCAATTTCCTCA | 55130 |
| rs759072435 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27817055 | GTGCCCGGCCTGTTA[C/T]GCAGTTTTATACATA | 55130 |
| rs759081412 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27901747 | TAAAGGGATCAATGC[-/A]ACAAGAAGAGCTAAC | 55130 |
| rs759100145 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27904455 | CACTCCAACCTGGGC[A/G]ACAGAGCGAGACTCC | 55130 |
| rs759102004 | snp | C/T | 1.65974e-05 | 0.0028807 | missense | ARMC4 | GRCh38.p7 | 10:27940805 | AGTCTAGTAGAGCAA[C/T]CTATAATAATAGATA | 55130 |
| rs759111530 | in-del | -/AATTT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27891951 | TTCTTAAGAACAAAG[-/AATTT]AATTTAATATATGGA | 55130 |
| rs759113174 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983191 | AGGCTCACCTCACCC[C/T]CTGGGAAATATCACT | 55130 |
| rs759116650 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27843909 | AACCACTACTAGCAA[A/C]AATGTTTAATTCTGC | 55130 |
| rs759122014 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27931440 | TAAATGTTTACTGCC[G/T]TCTCATCATCTACTT | 55130 |
| rs759122067 | snp | G/T | 4.95135e-05 | 0.00497537 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27944314 | CTGCCAAACATTTTA[G/T]ACTCTTGTGTGGAGA | 55130 |
| rs759132626 | in-del | -/AAC | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27972081 | TAAAGCAAAAATAGT[-/AAC]AACGTTTTGAGGGGT | 55130 |
| rs759141907 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27887978 | AAACAACCTACCAAG[A/G]CTGAATCATGAAGAA | 55130 |
| rs759158343 | in-del | -/C | 1.70339e-05 | 0.00291833 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940852 | AAATCTTAAAAAGAA[-/C]ATTTAAGGCATTCTT | 55130 |
| rs759169541 | snp | C/T | 1.71572e-05 | 0.00292888 | intron-variant | ARMC4 | GRCh38.p7 | 10:27862426 | AAACAAAAAGATGTG[C/T]TACTTACTGTATTTG | 55130 |
| rs759196673 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27840987 | TTAAATGAAATAAGG[A/G]ATAAAGCACATAGGC | 55130 |
| rs759246958 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27950626 | GAGTCTTGCTCTGTC[A/G]TGCGGGCTGGAGTGC | 55130 |
| rs759249115 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27854711 | CAGTGAGCCCAGATC[A/G]CGCCACTGAACTCCA | 55130 |
| rs759284687 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27838779 | CTGTTTGTGTATTTT[C/T]GACCCTCCAAAACTC | 55130 |
| rs759291788 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27836214 | TGCATGTATATGTGT[G/T]TGTATATAGAAAGGT | 55130 |
| rs759326402 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27838846 | TGCAATTATTTGAAA[C/T]GGATCTTTTATCAAC | 55130 |
| rs759349007 | snp | A/G | 1.65048e-05 | 0.00287265 | synonymous-codon, intron-variant | ARMC4 | GRCh38.p7 | 10:27944402 | TTGAGGATTATGACT[A/G]ATTTCCTTCAGTATT | 55130 |
| rs759352547 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27938703 | CTCCCAGGTTCAAGT[A/G]ATTCTCCTGCCTCAG | 55130 |
| rs759355578 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27952216 | GACATAATACAATGG[C/T]TATTTGACATATAAA | 55130 |
| rs759357387 | snp | A/G | 1.64972e-05 | 0.00287199 | missense, synonymous-codon, intron-variant | ARMC4 | GRCh38.p7 | 10:27812589 | CTGCAGCTTCCTGGA[A/G]ATCCTGGTCAGGGGA | 55130 |
| rs759359035 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27976472 | ATAGCAACAAATGAC[C/T]AAAAATAGAAAATTT | 55130 |
| rs759395361 | snp | C/G | 2.26134e-05 | 0.00336247 | synonymous-codon, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27985072 | ATCCAATTGCTTAAG[C/G]AGCATAGCAATCTTC | 55130 |
| rs759396635 | snp | A/T | 1.66504e-05 | 0.0028853 | missense | ARMC4 | GRCh38.p7 | 10:27860844 | TCTCAATTTATTGTT[A/T]TTCTGTGCAAGGGAA | 55130 |
| rs759408434 | snp | C/G | 1.64923e-05 | 0.00287156 | missense, utr-variant-3-prime | ARMC4 | GRCh38.p7 | 10:27936837 | AAGGGCTTAAGTCCT[C/G]CGTGCAGCCTAACGA | 55130 |
| rs759439808 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27880615 | AGTGAGTGGAATTAA[C/T]GCCTTTATAAAAGAG | 55130 |
| rs759440273 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27991155 | GGTGTTTTAGGAAGA[C/G]TATTAATTTCATCCT | 55130 |
| rs759442363 | in-del | -/TCA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27866779 | TAGACCAAGAAGAAC[-/TCA]TCACTCATTACAAAG | 55130 |
| rs759454797 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27823769 | AAAATTAATACATTA[A/C]CATAAGGTTCATGGT | 55130 |
| rs759476732 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27978454 | TTCCCTCCCATGTGC[A/G]TATTTTACTCAGGAG | 55130 |
| rs759542614 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27837465 | CAGAAATTTGATCAG[A/G]TTTCCACAATCAGAA | 55130 |
| rs759576110 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27850665 | AAATATCAAAAGAAA[A/C]GACTGCCTCATGTTA | 55130 |
| rs759585554 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27927383 | ATTATGGAAGATTTA[A/C]ATAGGAGAGAGGGAT | 55130 |
| rs759611236 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27987577 | AAATTGAAAGCTTCA[C/T]GCTACCTAGAGGTCA | 55130 |
| rs759613843 | in-del | -/AA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27977729 | ATGAAAAAAACAGAC[-/AA]AGAGTCCAAATAGAC | 55130 |
| rs759616361 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27909130 | TAAAATATAACTAAC[A/G]CCAATCTCTGAGCCT | 55130 |
| rs759619849 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27901639 | CAAGCAAATGGAAAG[C/T]AAAAAAAGCAGGGGT | 55130 |
| rs759638864 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27949523 | AAATGTCCACCAGTC[A/G]GAGCAAACAGTATAT | 55130 |
| rs759657003 | snp | C/T | 1.93295e-05 | 0.00310875 | intron-variant | ARMC4 | GRCh38.p7 | 10:27971317 | GAAGCTAATTCCCTT[C/T]ATTTAAAAAATGAGA | 55130 |
| rs759699202 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27988875 | AATTAAGTCAAGGAT[C/T]CTGAGATGGGGAGAC | 55130 |
| rs759708377 | snp | A/G | 1.65018e-05 | 0.00287239 | synonymous-codon, intron-variant | ARMC4 | GRCh38.p7 | 10:27944321 | ACATTTTAGACTCTT[A/G]TGTGGAGAATCAAGT | 55130 |
| rs759740542 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27834469 | TCATCACACGGCCAC[A/G]CCAAGACTCAAGGGA | 55130 |
| rs759750625 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27972007 | TGCAGAAATGGTAAA[A/C]ATAAATATACAAGAC | 55130 |
| rs759769961 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27819500 | TCCCAGTGCATTGGG[A/G]GGCCAAGGCAGGAGG | 55130 |
| rs759770375 | snp | A/G | 2.30041e-05 | 0.00339139 | intron-variant | ARMC4 | GRCh38.p7 | 10:27987554 | TTTCACTAAAAAATA[A/G]AAATAAAAAATTGAA | 55130 |
| rs759777891 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27990783 | GAATTGTGCATTCTT[A/G]AGGGGAAGACAGCCA | 55130 |
| rs759812116 | snp | A/G | 1.6534e-05 | 0.00287519 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27907771 | TCCATCTAAGCGATC[A/G]ATTATCCTATCGTGG | 55130 |
| rs759865443 | snp | A/T | | | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27936299 | TGAAAATGACCACTC[A/T]TTAAAGAGTAACTGG | 55130 |
| rs759868403 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27924589 | TTCAAAATAGAGAAA[C/T]CATACTAGCTAAATT | 55130 |
| rs759878920 | snp | C/T | 0.000129626 | 0.00804961 | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27958838 | GGTTAGTCAACTCAC[C/T]CAAGGCCATTGAGTA | 55130 |
| rs759905436 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27923247 | ACCCCATTTATATAC[G/T]GCATGCAAGGGCACA | 55130 |
| rs759930191 | snp | C/T | 3.33907e-05 | 0.00408586 | missense, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27961602 | TTCTGAATTTGCCAA[C/T]ATTCTGATGGCAAAT | 55130 |
| rs759938128 | snp | G/T | 1.65504e-05 | 0.00287662 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940553 | AGGGAAGCAGAACTG[G/T]CATGAGTACCTCTGA | 55130 |
| rs759959063 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27988208 | GCCTTTAAAAAATAT[C/T]AAGATGTTTTCATGG | 55130 |
| rs759962622 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27834857 | CACCTAAGTCATAGA[A/G]TCTCCAAAGAAATTG | 55130 |
| rs759966765 | snp | C/G | 1.64776e-05 | 0.00287028 | stop-gained, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27944925 | CTGAAATCCCTCATT[C/G]AACACAACGCAATCA | 55130 |
| rs759981023 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27842320 | TCCTGCCCATGTGGA[A/G]AATCTCTACACTGTA | 55130 |
| rs760004086 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27820930 | AAGATTACAGGCATG[C/T]GCCACCACACCGGCT | 55130 |
| rs760018378 | snp | C/T | 1.64996e-05 | 0.0028722 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984178 | GAGCCTGAGAAAACA[C/T]CAAACCTGAGGTATA | 55130 |
| rs760028538 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997872 | TCCATGTAAATACAC[A/G]GCACACACCTTTGAA | 55130 |
| rs760067313 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27860098 | ATTTTACTAAGTACA[C/T]TTCTATGCTTTAATT | 55130 |
| rs760068715 | snp | C/T | 1.70165e-05 | 0.00291684 | intron-variant | ARMC4 | GRCh38.p7 | 10:27995184 | TTAGCACACGCACTA[C/T]ATCAGAGCAGAAAGA | 55130 |
| rs760121653 | snp | A/G | 3.30017e-05 | 0.00406199 | missense, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983947 | GAATTTGTCTCCACG[A/G]TGGGGCTCGACATCC | 55130 |
| rs760126316 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27928692 | ATCAAGAGGCAAAAT[A/C]ATCTTATACAGATGA | 55130 |
| rs760166764 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27838571 | CAAAAGGGCCAAGTC[A/G]GAAGGAAAAGACATT | 55130 |
| rs760191231 | snp | C/T | | | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27857664 | AAACTGAACTCATTA[C/T]ATTTCAGACCCTGCT | 55130 |
| rs760199310 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27993315 | AACTTCTGGAGAAAG[G/T]TACCACTGGCACAGT | 55130 |
| rs760207733 | snp | G/T | 1.64906e-05 | 0.00287142 | synonymous-codon, intron-variant | ARMC4 | GRCh38.p7 | 10:27971158 | TGGTTCCCATCTCTT[G/T]GTCATTTGATTCCTC | 55130 |
| rs760211744 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27951992 | AGACAGGAGAATTGC[C/T]TGAACTGGGGAGGCA | 55130 |
| rs760236931 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27817121 | ATATTCTCATTCTCC[C/G]TCTCTCACTGTAGGA | 55130 |
| rs760247893 | in-del | -/CCCCCA | 1.64795e-05 | 0.00287045 | cds-indel | ARMC4 | GRCh38.p7 | 10:27940651 | GCCAACAGAGGAATG[-/CCCCCA]GCTTTGCGGATGGCT | 55130 |
| rs760262894 | snp | C/T | 3.9185e-05 | 0.00442617 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27944230 | TACTCACCAGTTTGG[C/T]GATACCCCCGTGCTG | 55130 |
| rs760296710 | in-del | -/AA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27885792 | ATATATATTATATAT[-/AA]AATATATATAAAATA | 55130 |
| rs760325470 | snp | C/T | 0.000198459 | 0.00995941 | missense | ARMC4 | GRCh38.p7 | 10:27935247 | ATGGCTTTGTATTCC[C/T]GAAACCTAAGTTCAT | 55130 |
| rs760331289 | snp | A/C | 5.02719e-05 | 0.00501332 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944183 | TGTGTGCAGTGGCGG[A/C]TGGCACTAGATGACG | 55130 |
| rs760341958 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27865778 | TACAACAAACCAAAC[C/T]AAACTCCTACTAAAT | 55130 |
| rs760343073 | in-del | -/AC | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27832538 | CACACACACACAGAC[-/AC]ACACACACACACACA | 55130 |
| rs760350019 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27837664 | GGATTAAAATTTAAA[C/T]GTGGGTCATAAAGAA | 55130 |
| rs760377894 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27953236 | TAACTATAGGTATTA[C/T]GTTGTACAGCAGATA | 55130 |
| rs760409087 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27856397 | AACCCTTTTGAAACT[A/T]GCTCTTCCTTTGGCT | 55130 |
| rs760438280 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27862987 | GCAAACACTGAATCA[A/G]CCAATACTAAACTTT | 55130 |
| rs760457381 | snp | G/T | 4.77293e-05 | 0.00488491 | missense | ARMC4 | GRCh38.p7 | 10:27985200 | GGATTTTTACTATGG[G/T]GTCTCTGTTAGCTGC | 55130 |
| rs760457835 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27895957 | CCCTGAAAAATAGGA[A/C]CTTTTAAGAAGAAAC | 55130 |
| rs760463853 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27940088 | TAATAAACATGCTGA[A/G]CAAACTTTCTTAGGA | 55130 |
| rs760466034 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27928791 | GAACCTATTTCTACC[A/G]CAACAATACTAGCCT | 55130 |
| rs760516852 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27823351 | TAGATCAAAGTGTAG[A/G]TGGCAATTCTCTGGA | 55130 |
| rs760522414 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27908942 | TAAAAATTATTTTAA[A/G]GCAAAGCTTAAGTAA | 55130 |
| rs760530771 | snp | G/T | 1.66524e-05 | 0.00288547 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27862449 | TGTATTTGCCAGTTT[G/T]GACAATAAAGGAACA | 55130 |
| rs760536322 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27980010 | AATAGAATTAAAAGT[A/C]CCCAAGTAAACTCTT | 55130 |
| rs760540781 | snp | C/T | | | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27936576 | TCTTTTCTTTTCTAT[C/T]CTAAGAATCCCTTCA | 55130 |
| rs760547441 | snp | A/G/T | 4.82186e-05 | 0.00490993 | missense, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27985088 | AGCATAGCAATCTTC[A/G/T]TCTTAATTTCACTTT | 55130 |
| rs760567171 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27929754 | TTTAATCAATGGCTT[A/G]TGTCATTAAAAGAAG | 55130 |
| rs760570225 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27912562 | CAGTTTGTGCCCATA[A/C]TGTGGGCACAGGCAA | 55130 |
| rs760572595 | snp | A/G | 1.66407e-05 | 0.00288446 | missense | ARMC4 | GRCh38.p7 | 10:27862600 | AAACCACCAACAAAG[A/G]AACGAACCATTTCCC | 55130 |
| rs760612542 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27891686 | TCTTAATAAAAACTT[C/T]TAAAAACTCATTAAT | 55130 |
| rs760615997 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27839080 | CTGTCGTTTTCTTCT[A/G]TTTGTGATCAGAAAA | 55130 |
| rs760621538 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27813375 | AAATGTCTGTTGCTA[C/T]ACGTATTTTTCCCTT | 55130 |
| rs760626579 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27923451 | CATAACCATTAGAAA[C/T]ATTTATGCACCAAAT | 55130 |
| rs760630017 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27960649 | GCCACTGCACCCTGC[C/T]AAAATATTATTTATT | 55130 |
| rs760637098 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27863478 | ATGTCCAAGAATGAC[C/G]ATATTGAGTAGGGGG | 55130 |
| rs760664232 | snp | C/T | 1.65203e-05 | 0.002874 | missense | ARMC4 | GRCh38.p7 | 10:27939989 | TCCTTTCTGCTTTGA[C/T]TGCAGCCCGGTAGTT | 55130 |
| rs760679148 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27900718 | AAAGGTTATCAGATA[C/T]TGAAGGTCATCTTAG | 55130 |
| rs760680193 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27888125 | GCTGTGATAAACATA[C/T]AAGTACATGTATCTT | 55130 |
| rs760711698 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27913416 | CATTAATTTGCTTAG[G/T]ATAATGTTCTCCAGC | 55130 |
| rs760744991 | in-del | -/TCCT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27900223 | ACCTGCAGCAGAGAG[-/TCCT]GACTGTTAGAAGGAA | 55130 |
| rs760780467 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27854318 | TTTAAAAAGTTAAAG[A/G]TACACATACCGTATG | 55130 |
| rs760784496 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27989053 | GAACATAGGGGCCTC[C/T]AGAAGCTGGAAAAGC | 55130 |
| rs760790967 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27871787 | TTTGAAGTCAGGTAG[C/T]GTGATGCCTGCAGCT | 55130 |
| rs760791598 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27937470 | AATTTCTCCAATCAA[A/G]TTTCTATGCCCAGAG | 55130 |
| rs760820385 | snp | A/G | 0.000100115 | 0.00707443 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944443 | CAATCTGTGTGAGAA[A/G]AAAAAAGATGAGTGG | 55130 |
| rs760821261 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27975741 | TAATAAACAAACAAT[A/C]TTAATTCTATACAAA | 55130 |
| rs760828046 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27821177 | CAGTCTCAATCAAGG[A/G]TGTAGAATTGGAAGT | 55130 |
| rs760828247 | snp | C/T | 1.70151e-05 | 0.00291672 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983819 | GTCCACTGGCTTTAG[C/T]TACGTTTTTAAAAAT | 55130 |
| rs760845528 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27874348 | TTGGAGCATTTAGTC[C/T]ATTTACATTTAAGGT | 55130 |
| rs760862255 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27957571 | TTTAGAATTAGGGTA[C/T]AGCATCATCACCTAT | 55130 |
| rs760864014 | snp | A/G | 1.6516e-05 | 0.00287362 | intron-variant | ARMC4 | GRCh38.p7 | 10:27934992 | ATATAAAATCTTTCC[A/G]TCTCCAGGGCCACTT | 55130 |
| rs760874530 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27990339 | CGTTGGTCTGTTTAT[C/T]TATTTATTATTTATT | 55130 |
| rs760879162 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27911446 | AAATAATGAGGACTG[A/C]CTGTATTTTAATGGA | 55130 |
| rs760884127 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27822486 | AGGCATTGCAGTGAC[A/G]TTGTAGCACTCATGC | 55130 |
| rs760892247 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27957162 | ATATCCATATAAAGT[C/T]AGCAAATACAGCAAT | 55130 |
| rs760910355 | snp | C/T | 1.65883e-05 | 0.00287991 | synonymous-codon, utr-variant-5-prime, intron-variant | ARMC4 | GRCh38.p7 | 10:27981514 | TTTTTCTCTTAAAAA[C/T]GTGACAAGGTTTTTA | 55130 |
| rs760923906 | snp | A/G | 3.47633e-05 | 0.00416898 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944473 | GCGAATATGTAACCC[A/G]TGCTATGTTTTTAAA | 55130 |
| rs760935246 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27910274 | GCACATTTGATCAGC[A/G]CTTGTTAAACGATTC | 55130 |
| rs760954998 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27860986 | TGACTACCTAGGTGA[C/T]GTTTTGAAGGAACTA | 55130 |
| rs760968744 | snp | C/T | 3.30447e-05 | 0.00406464 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27994951 | TTCAAATGCTGAGGG[C/T]GCCAAACTTGTGTTC | 55130 |
| rs760977946 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27957787 | GCTCATAGCTCTGGA[C/T]GAATAATAAGCTATA | 55130 |
| rs760987566 | snp | G/T | 1.65078e-05 | 0.00287291 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27812596 | TTCCTGGAGATCCTG[G/T]TCAGGGGACCCAACC | 55130 |
| rs760999814 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27925713 | TGATAAAATACATAC[A/G]CTTTAAACCTAAGGT | 55130 |
| rs761010336 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27859178 | ATATTGAGACAATGG[C/T]CTTTTTAGCATTCCT | 55130 |
| rs761022832 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27830987 | GTTCTATCAGGTAGA[G/T]ATACTGCTGATCAGC | 55130 |
| rs761074459 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27918595 | ACCACTAACATCACA[A/C]TTAATGGTGAAAAAT | 55130 |
| rs761097127 | snp | C/G | 1.64925e-05 | 0.00287158 | missense | ARMC4 | GRCh38.p7 | 10:27940766 | ACAGACTCGATTGGG[C/G]AGGTTTTGTGGAATC | 55130 |
| rs761135975 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27888049 | AAACAATAATAAAAA[G/T]CCTCCCAACGAAGAA | 55130 |
| rs761174302 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27998091 | ATTCGGTAATCACAT[C/T]GTTAACACTTAAACA | 55130 |
| rs761181016 | snp | A/T | 4.94442e-05 | 0.00497188 | missense | ARMC4 | GRCh38.p7 | 10:27940683 | GGCTTCTTTATTCGT[A/T]TGACTCTTACTGCAG | 55130 |
| rs761191394 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27886673 | CAGGATTTAAAAGAC[A/G]AATGCATAAAAATTA | 55130 |
| rs761193360 | in-del | -/GGATGTA | 1.65004e-05 | 0.00287227 | frameshift-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983972 | CATCCATTTGAAAAT[-/GGATGTA]TCATAATCTGAAACC | 55130 |
| rs761227155 | snp | A/T | 1.64893e-05 | 0.0028713 | missense, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984202 | AGGTATATTCAATAG[A/T]TTCCAAGACTGTTTG | 55130 |
| rs761272238 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27862775 | TTATATATTATTTCT[A/T]CATGTATATGTATAA | 55130 |
| rs761302342 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27966674 | CCACTTAGGCAAGAT[G/T]TGACACAGAGAACCT | 55130 |
| rs761310758 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27840942 | TTAAAATGGGAGAGT[A/C]ATGCCTGCACCACAG | 55130 |
| rs761314852 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27980378 | TGCATCAAAGGACAC[C/T]ATCAAGAAAGTTATA | 55130 |
| rs761355968 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27889242 | ACCCAACCTTCTGAC[C/T]AGAAACTGAGCAAGG | 55130 |
| rs761374291 | snp | C/T | 1.64817e-05 | 0.00287064 | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27936690 | GTGTTTCAGAAGCCG[C/T]ATCTTCATTTCAGAA | 55130 |
| rs761400699 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27859369 | TTCAAACATATATTG[A/G]GTTTAATTTCAGAAA | 55130 |
| rs761407359 | snp | A/C/G/T | 6.61011e-05 | 0.00574867 | synonymous-codon, intron-variant | ARMC4 | GRCh38.p7 | 10:27944297 | ATTCGCGATAGTCTC[A/C/G/T]GCTGCCAAACATTTT | 55130 |
| rs761418844 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27953355 | TAAAAAATCTTATAA[A/C]TATCTTGGCACTTGT | 55130 |
| rs761439006 | snp | A/G | 1.6651e-05 | 0.00288535 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984332 | TTAAATACTTTAAAC[A/G]GAATCTAGGAAACAC | 55130 |
| rs761475632 | snp | A/G | 1.65891e-05 | 0.00287998 | intron-variant | ARMC4 | GRCh38.p7 | 10:27935261 | CCGAAACCTAAGTTC[A/G]TCATAAGAAAGAGGA | 55130 |
| rs761509351 | in-del | -/TATATA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27827384 | CACACACACACTATA[-/TATATA]TATATATATATATAT | 55130 |
| rs761516242 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27972694 | AGAGGAGCACACATA[C/T]TAATAGAGGATCAAT | 55130 |
| rs761524581 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27928850 | CAGTCACTTTACTTA[C/T]ATAAATTCACTTAAT | 55130 |
| rs761529193 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27886960 | AATGAAGAAAATGAG[G/T]AATAAAAGGCTATAA | 55130 |
| rs761535514 | snp | A/C | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27960754 | ATGATTAAATCAAGC[A/C]AAGCCACTGGCAAAT | 55130 |
| rs761555626 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27839331 | GGCTTCACTCAACTC[A/G]GGAAAGAGAGGCTCA | 55130 |
| rs761558479 | snp | A/G | 1.64811e-05 | 0.00287059 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27860694 | TTGGTACAAGGCCTG[A/G]GCTGTCGCCCGATGC | 55130 |
| rs761559091 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27914890 | ACAGAAAAACAAAGA[A/G]AAAAGCCTGACCTTT | 55130 |
| rs761585897 | snp | C/T | 3.29783e-05 | 0.00406055 | missense, intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27971186 | CTCCAAAAATTAATT[C/T]GGTTCTTCTCCAGTG | 55130 |
| rs761601278 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27844029 | ACAGCAAGTTCCCAT[C/T]TCTACAAACAATAAA | 55130 |
| rs761647807 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27820033 | ACGCTCATGGTGATT[A/C]TTTTGCCAGTTCAGA | 55130 |
| rs761650817 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27877488 | CCCTGCAGGTCCCTC[-/T]TGAAGTTTATTTGTT | 55130 |
| rs761673868 | snp | C/T | 7.63466e-05 | 0.00617798 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27968987 | GTTTTCCTGTGTGTT[C/T]GTCCTCTTGGATTTC | 55130 |
| rs761685745 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27874055 | CTGTATTGGGTGCAT[A/G]TATATTTAGGATAGT | 55130 |
| rs761700557 | snp | C/T | | | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27981881 | AGAAGTGAGAGCTTC[C/T]TTCTCTCCGCTCTCC | 55130 |
| rs761707365 | in-del | -/AT/ATAAAT | 0.000402495 | 0.0141805 | intron-variant | ARMC4 | GRCh38.p7 | 10:27853393 | TAAATAAATAAATAA[-/AT/ATAAAT]AAGTAAGCCCTAACT | 55130 |
| rs761710990 | snp | A/G | 1.7856e-05 | 0.00298792 | synonymous-codon, intron-variant | ARMC4 | GRCh38.p7 | 10:27944240 | TTTGGTGATACCCCC[A/G]TGCTGCCTCACCACC | 55130 |
| rs761718691 | snp | G/T | 0.000231035 | 0.0107454 | missense | ARMC4 | GRCh38.p7 | 10:27995102 | CCAGTTCCATGTCCG[G/T]CAGCAGTCCACTGCG | 55130 |
| rs761723190 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27883764 | CTTCAGTTTAGTTGA[A/G]AGTACAATAACTGAA | 55130 |
| rs761762475 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27986897 | ACAGTGGAATATGGC[-/T]GAGAAAAGTGGAAAG | 55130 |
| rs761767013 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27827572 | TCTTCCCCAGGCATC[A/C]CATCCAAAATGTCAC | 55130 |
| rs761773632 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27871477 | TTTCCTCTAGGGCTT[C/G]TATGGTTTTAGGTCT | 55130 |
| rs761798726 | in-del | -/CTC | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27954119 | GATGCCTCTTATTCA[-/CTC]CTCAACTCATATATT | 55130 |
| rs761799709 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27815288 | CCTCTTCCTTTCTAA[C/T]GATTCCATTATCATT | 55130 |
| rs761805095 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27890424 | ACCAACTGTGCTTTC[A/G]AAATTAAGTGGTTAA | 55130 |
| rs761810993 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27866000 | GCTTATTTGGAAAAA[C/T]AGTTAATTGCCATTC | 55130 |
| rs761829864 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27976208 | ACAAGAGACCATTTC[C/T]ATTCAATTTTTTACT | 55130 |
| rs761848732 | snp | C/T | 1.75739e-05 | 0.00296423 | intron-variant | ARMC4 | GRCh38.p7 | 10:27907642 | GATTCTAGAAGAGAC[C/T]GACTTGCAGTCCGTT | 55130 |
| rs761855617 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27823522 | TATCAGTAAAATTAG[A/G]ATTTTTAATAGTACT | 55130 |
| rs761856113 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27901785 | AATATATATGCACCC[A/G]GTACAGGAGCACCCA | 55130 |
| rs761864532 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27837214 | CTGCCCTGTGACCAC[A/G]TGGTCCCGTACTGGT | 55130 |
| rs761882522 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27955805 | AGTCTTTAACAAAGG[G/T]TTTCAAGTCTGAAAA | 55130 |
| rs761904767 | snp | C/T | 8.11655e-05 | 0.00636994 | missense | ARMC4 | GRCh38.p7 | 10:27985209 | CTATGGGGTCTCTGT[C/T]AGCTGCCAAAAAAAA | 55130 |
| rs761929411 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27977917 | ACTGGGACTCTCATA[C/T]ATTGCCTACATCAAT | 55130 |
| rs761943686 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27822545 | ACTGTGTCCGCCTAT[A/G]GAATGGCTTCCCAAC | 55130 |
| rs761998344 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27938445 | GGCCTCAGAAGAAAC[C/T]AACTTTGGTCTGAAA | 55130 |
| rs762000086 | snp | A/C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27925888 | ATAAGAATTTTAAAG[A/C/G]AGTAACATTTGGGAG | 55130 |
| rs762002566 | snp | A/G | 0.000838574 | 0.0204593 | intron-variant | ARMC4 | GRCh38.p7 | 10:27853396 | AATAAATAAATAAAA[A/G]TAAGCCCTAACTATA | 55130 |
| rs762030460 | in-del | -/AG | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27957216 | ACGGCAGGAAAAGGA[-/AG]AGAGAGGGATGCAAG | 55130 |
| rs762038993 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27832773 | TACACTCACAATGGG[C/T]ATCCTATTTATCATG | 55130 |
| rs762040375 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27941852 | AGATACTGCCCGTAA[C/T]CACCAATCTCAAATT | 55130 |
| rs762048112 | snp | A/C | | | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999335 | GAAACCCCTTTTTAC[A/C]TTTTTCCATAGGCTT | 55130 |
| rs762051082 | snp | A/G | 1.65839e-05 | 0.00287953 | missense | ARMC4 | GRCh38.p7 | 10:27939998 | CTTTGATTGCAGCCC[A/G]GTAGTTTTCCTAGGA | 55130 |
| rs762056383 | snp | A/T | 3.3024e-05 | 0.00406336 | missense, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983917 | GTTTCACCAGCACAT[A/T]ACAAATTTCCCCACG | 55130 |
| rs762080611 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27944494 | TGTTTTTAAAAATTC[C/T]GAGTATACCTAAAAT | 55130 |
| rs762088705 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27899680 | GTTTTCCCCTCACAG[C/T]GTAAACAAAGCCTCC | 55130 |
| rs762109038 | snp | C/T | 1.64798e-05 | 0.00287047 | missense | ARMC4 | GRCh38.p7 | 10:27944884 | CAACATCTCTGATGG[C/T]CAACTGGCAGGTTTC | 55130 |
| rs762110753 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27844153 | TGAGCTATGATCGTG[C/G]CACTGTACTCCAACT | 55130 |
| rs762128628 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27880692 | TGAGGACACAGCAAC[C/T]AAGTGCCATCTTGGA | 55130 |
| rs762143743 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27911489 | TACAGTCTTGTGAGG[G/T]TGATAAACAGACCAT | 55130 |
| rs762152739 | snp | G/T | 1.64811e-05 | 0.00287059 | missense | ARMC4 | GRCh38.p7 | 10:27935142 | ACAATGACTCGGTTT[G/T]CACGTTCTTGGCAGC | 55130 |
| rs762153634 | in-del | -/T | | | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27857804 | TCAATTACTTATGAA[-/T]AGGCGACACGGTGAC | 55130 |
| rs762156937 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27818363 | ATTTTCTCACTCCTT[C/G]TCCCAAGTAGATGAT | 55130 |
| rs762164690 | in-del | -/T | 1.65269e-05 | 0.00287457 | intron-variant | ARMC4 | GRCh38.p7 | 10:27981630 | ACATAAGAACAATTG[-/T]TAAGAAGCTGATCAA | 55130 |
| rs762164748 | snp | A/C | 1.65111e-05 | 0.0028732 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27995107 | TCCATGTCCGGCAGC[A/C]GTCCACTGCGTCAAT | 55130 |
| rs762221801 | snp | A/C | 1.6571e-05 | 0.0028784 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27812618 | GACCCAACCATATCC[A/C]GTAGAAGCTGTCACA | 55130 |
| rs762250505 | snp | C/T | 1.64988e-05 | 0.00287213 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27994969 | CAAACTTGTGTTCCA[C/T]TCAAGTGGTTCCACA | 55130 |
| rs762269366 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27920556 | AGATTAAATGATTCA[C/T]ATAATTACTCTCCAT | 55130 |
| rs762280818 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27854047 | ACCCAATGATAAGAA[A/G]ACAACCTAATTAAAA | 55130 |
| rs762281097 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27871125 | GATGAGCATTTTTTC[A/G]TGTGTCTATTGGCTA | 55130 |
| rs762304963 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27847467 | CCCACAGCCAATATC[A/G]TCCTGAATGGGCAAA | 55130 |
| rs762307637 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27921831 | GGCAATAGAGCAGTA[-/T]TTTTATTTTTTTTTT | 55130 |
| rs762327505 | in-del | -/TTTA | 1.65094e-05 | 0.00287305 | frameshift-variant, intron-variant | ARMC4 | GRCh38.p7 | 10:27944309 | TCGGCTGCCAAACAT[-/TTTA]TTTAGACTCTTGTGT | 55130 |
| rs762333658 | snp | C/G | 1.65285e-05 | 0.00287471 | missense | ARMC4 | GRCh38.p7 | 10:27940791 | GGAATCATGTGCACA[C/G]TCTAGTAGAGCAACC | 55130 |
| rs762353585 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27970083 | TGCAGCCTGGGTGAC[A/G]GCGAGATTCTGTCTC | 55130 |
| rs762385193 | snp | C/T | 1.64906e-05 | 0.00287142 | missense | ARMC4 | GRCh38.p7 | 10:27935014 | GGGCCACTTACATCA[C/T]ACTTTCAGGTTCTAC | 55130 |
| rs762408624 | snp | C/T | 1.64928e-05 | 0.00287161 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27940716 | CCACAGGGCCAGTGC[C/T]CCACAGCGAGCCACT | 55130 |
| rs762410535 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27886127 | AAGTAATAATGACCA[A/G]AAATGTCCCAAATTT | 55130 |
| rs762412175 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27972464 | GAAAGTGTTTACACA[C/T]ATCAATTAAATGAGA | 55130 |
| rs762423616 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27934356 | CCAGGTTCCTCCTTT[A/G]TTGGAGTAAAGATAT | 55130 |
| rs762458518 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27897602 | TAATAGCCCAATTTG[C/T]CACCCATTCTTACAT | 55130 |
| rs762489572 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27996873 | GACATCTGACTACTT[C/T]CCTATATATTCTAGT | 55130 |
| rs762489765 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27841286 | TTAATTCTTCCTGTT[C/G]CCTTAATCTCTCATC | 55130 |
| rs762492482 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27969194 | CTTTCACTCTTTCAG[A/C]ACAGCCCTATGTTTT | 55130 |
| rs762500609 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27906627 | CAAAACACCCATCAA[C/T]GATAGACTGGATAAA | 55130 |
| rs762518629 | snp | G/T | 1.6531e-05 | 0.00287493 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27860831 | CTGCTAGATGATGTC[G/T]CAATTTATTGTTATT | 55130 |
| rs762522503 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27982980 | GGCTAGGTTATTAGG[C/T]TCCGTCATTAGAATC | 55130 |
| rs762541691 | snp | C/T | 8.32244e-05 | 0.00645022 | missense, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27961635 | GCACTTGCTTCCTGA[C/T]GATGGTCAGGTGGTT | 55130 |
| rs762544821 | snp | C/T | 1.64855e-05 | 0.00287097 | missense, utr-variant-3-prime | ARMC4 | GRCh38.p7 | 10:27936816 | GTGTTATTGAGTAGA[C/T]TGGCCAAGGGCTTAA | 55130 |
| rs762560421 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27956532 | GGTGCCTGGACAATA[C/T]GGGCATCTTATCCTG | 55130 |
| rs762580843 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27916221 | AAAGCTGAGCAGGGT[A/G]AGGAGGGCAGACATA | 55130 |
| rs762604830 | in-del | -/AC | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27979447 | CACACACACCCATAC[-/AC]ACACACACACACACA | 55130 |
| rs762615436 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27841986 | AGTCCTCAGAAATTT[A/T]AGGCACATTCCTACC | 55130 |
| rs762619940 | snp | A/G | 1.64825e-05 | 0.00287071 | missense | ARMC4 | GRCh38.p7 | 10:27860747 | GATAACGCACTAGTG[A/G]AGCCACTGCTTTGTG | 55130 |
| rs762654747 | in-del | -/AG | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27882150 | TCCAGCCTGGGTGAC[-/AG]AGTGAGACCTTGTCA | 55130 |
| rs762654939 | in-del | -/AACA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27902096 | AAGAACAGAAATGAT[-/AACA]AACAGTCTCTCGGAC | 55130 |
| rs762663948 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27885020 | AGAAGATCTGAAGAC[A/T]TACGAAGAAACAGGA | 55130 |
| rs762667809 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27866651 | GAAGCTTCCACTCAT[G/T]GTAGAAGGTGAAAGG | 55130 |
| rs762668569 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27903120 | TCAAGTCAGCTTCAT[C/T]CCTGGGATGCAAGGC | 55130 |
| rs762685579 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27827715 | TAACTCATCTTCCAG[C/T]CCCGTTCCCATCCAT | 55130 |
| rs762700984 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27933284 | AACAAATAAGAATGT[-/A]ACTCCAGACAATTGA | 55130 |
| rs762710621 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27815450 | CACTGACTCCAGGCT[A/G]CTGTCTGCCTTCAGC | 55130 |
| rs762721066 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27883970 | ACACATATGAGCATT[C/G]TAGAAAAAAGGAGAA | 55130 |
| rs762723536 | snp | A/G | 1.65211e-05 | 0.00287407 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27944301 | GCGATAGTCTCGGCT[A/G]CCAAACATTTTAGAC | 55130 |
| rs762739207 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27991056 | AAAGAATCAAAGTGC[C/T]TTGGTTCTATGTACC | 55130 |
| rs762776809 | snp | C/T | 1.64925e-05 | 0.00287158 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27944382 | TCAACAATATTCTGT[C/T]TGATTTGAGGATTAT | 55130 |
| rs762781312 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27816842 | CAACCTCCGTCCCCT[A/G]GGGTTCAAGTGATTC | 55130 |
| rs762786225 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27868442 | CCCAAATGCCCATCA[A/G]TGATACACTGGATAA | 55130 |
| rs762790704 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27931427 | TGTGCATTACTAATA[A/C]ATGTTTACTGCCTTC | 55130 |
| rs762796360 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27892804 | TTGATTCTGCTACTT[C/T]GTTGCCTGGCTCAAT | 55130 |
| rs762803227 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27989262 | GGACTTTATGAGTCC[A/G]ATTCTGCTGGGTGCA | 55130 |
| rs762841130 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27964321 | ATCTTGGCTCCTAGA[G/T]GAGCTGGGGTAGTCT | 55130 |
| rs762843920 | snp | A/G | | | synonymous-codon, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983879 | TGCACTGCAAGTAAT[A/G]CACAGAGTCTCACCA | 55130 |
| rs762890151 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27836123 | CTGCATAAAATTGGA[C/T]CCATGCACTTCAAAC | 55130 |
| rs762910121 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27906039 | ATTAAACTAAAAAGC[-/T]TCTGCACAGCAAAAG | 55130 |
| rs762943979 | in-del | -/T | | | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:28000904 | ATTTATCATGACTTG[-/T]TTTTTTTTTTTTCTT | 55130 |
| rs762954275 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27928605 | AGTTTAATGCGAATT[A/G]TTTGCCATTTAAGGC | 55130 |
| rs762954879 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27955167 | AGTGGACGAACAGTG[A/G]GCATTGTTTTCCGTT | 55130 |
| rs762995394 | snp | A/C | 1.96019e-05 | 0.00313058 | stop-gained | ARMC4 | GRCh38.p7 | 10:27987542 | ATTTGACTGTTGTTT[A/C]ACTAAAAAATAAAAA | 55130 |
| rs762998733 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27891831 | GGCATGAAAATAATC[A/G]TGTGATACGACACAA | 55130 |
| rs763005588 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27825779 | AATCCTTTACAAATT[A/G]GACTTTGCCTAGGGC | 55130 |
| rs763015694 | snp | C/T | 1.64874e-05 | 0.00287113 | missense, synonymous-codon, intron-variant | ARMC4 | GRCh38.p7 | 10:27812517 | CATTTAAATTTCAAG[C/T]GTATCTTGCCTTCTC | 55130 |
| rs763052085 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27937713 | ATGTGTCACCCATGG[A/G]GGCCACTAGAAGAAA | 55130 |
| rs763089047 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27913086 | TAGAAAGACTCTAGA[A/C]ATCTTTTTTGTCAGA | 55130 |
| rs763099852 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27939118 | TTACAATAAGTAAAC[C/G]AGTAAAAAGATAAAA | 55130 |
| rs763115959 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27848597 | TCCTGCACAGCAAAA[C/G]AAACTACCATCAGAG | 55130 |
| rs763145085 | snp | A/T | 3.29788e-05 | 0.00406058 | missense, intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27971207 | TTCTCCAGTGACCTT[A/T]TGTCTGAACCAGAAA | 55130 |
| rs763159743 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27827633 | CTCTTGAATCCACCC[A/G]TTTCTCTTCATCTCC | 55130 |
| rs763171170 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27889966 | AAGAAAGAGAGTATA[C/T]GGACTTGAGGGTATT | 55130 |
| rs763176131 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27986175 | CGAAAAGGAGACAAA[A/G]GAATCAACCATTTAT | 55130 |
| rs763178072 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27850271 | CCAACATGGTGAAAC[C/T]CCCTCTCTATCAAAA | 55130 |
| rs763192563 | snp | A/G | 6.60371e-05 | 0.0057458 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944996 | AGAGAAAGGTTAAGG[A/G]ACACCGCATTCCCAT | 55130 |
| rs763200521 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27941664 | AAAGGCAATTTACTA[C/T]AAGGATTAAGCAGTA | 55130 |
| rs763211692 | in-del | -/GC | | | intron-variant, frameshift-variant | ARMC4 | GRCh38.p7 | 10:27853339 | TGTCACTGCACTCTA[-/GC]CTGGCGACATGGCGA | 55130 |
| rs763228791 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27933789 | AGTCCAGCCAGTATG[C/T]TTCCCTTAAAGTAAT | 55130 |
| rs763235646 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27930626 | GCCAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAG | 55130 |
| rs763241692 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27864513 | AAGTGAGAGTGGAGA[A/G]TGAGGTGAGAGCGGG | 55130 |
| rs763254576 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27987197 | AAAGCAGAAATTTGA[C/T]AGGAGCATAATATTG | 55130 |
| rs763275340 | snp | C/G/T | 3.29572e-05 | 0.00405928 | missense | ARMC4 | GRCh38.p7 | 10:27944895 | ATGGCCAACTGGCAG[C/G/T]TTTCTTGAGCTAAGC | 55130 |
| rs763290979 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27947859 | TAACATTCTTAATCG[C/T]TCGTGCTGAGGACTT | 55130 |
| rs763298147 | snp | A/G | 1.65048e-05 | 0.00287265 | missense, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983932 | AACAAATTTCCCCAC[A/G]AATTTGTCTCCACGG | 55130 |
| rs763310105 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27934783 | GGGAAATTGATTACC[A/G]TGTATTGTAAATCCT | 55130 |
| rs763316349 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27987265 | ACATTTGACTTTTTA[C/T]CTTGTAGATTGTAGA | 55130 |
| rs763367784 | in-del | -/AAC | 1.65611e-05 | 0.00287755 | cds-indel | ARMC4 | GRCh38.p7 | 10:27862461 | TTTGGACAATAAAGG[-/AAC]AACTCCATGATCTGT | 55130 |
| rs763411079 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27907194 | GTCTCCTGTTTTTAG[C/T]GACAGATAAGAAAAG | 55130 |
| rs763419640 | in-del | -/AAAAAAAG | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27882170 | GAGACCTTGTCATAA[-/AAAAAAAG]AAAGAAAGAAAGAAA | 55130 |
| rs763436066 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27859617 | TGGTTGTCATAGGCT[A/C]CAAATGAAGGTAATA | 55130 |
| rs763440573 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27970221 | TTTGACGCCTGTTTA[C/T]AGAAGGTCCTAAATG | 55130 |
| rs763449639 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27856499 | AAAGTGAAAATGTAG[A/G]TATTTCCCAGGGCTC | 55130 |
| rs763461184 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27876467 | CAGCAAACTCCAGCA[C/G]ACCTGCAGCTGAGGG | 55130 |
| rs763471776 | snp | C/T | 1.64822e-05 | 0.00287068 | missense | ARMC4 | GRCh38.p7 | 10:27935151 | CGGTTTTCACGTTCT[C/T]GGCAGCATTCTCCCA | 55130 |
| rs763477207 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27835099 | CCTGGCAGGGCAGGG[C/T]AGAGAACAAAACCAC | 55130 |
| rs763489219 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27923048 | AACAAAAATGCAAAC[A/C]TTTCTAAAGAACAAC | 55130 |
| rs763504572 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27993472 | CTGGGCAACATGGGG[-/A]AACCCCGTCTCTACT | 55130 |
| rs763518342 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27820685 | TTTATTTTGCCTTAA[G/T]TTTCTCACATTAACC | 55130 |
| rs763523325 | snp | A/G | 3.29935e-05 | 0.00406149 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984181 | CCTGAGAAAACATCA[A/G]ACCTGAGGTATATTC | 55130 |
| rs763528082 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27860333 | TGGCATGCACCTGTA[G/T]TCCTGGCTACTTGGG | 55130 |
| rs763528943 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27925067 | TAAAAAGCCAGAAAA[A/G]GAAAACAGAAAAAAG | 55130 |
| rs763561367 | snp | A/G | 3.3036e-05 | 0.0040641 | missense | ARMC4 | GRCh38.p7 | 10:27935235 | ACCAAGGTTTCAATG[A/G]CTTTGTATTCCCGAA | 55130 |
| rs763605201 | snp | A/G | 1.64784e-05 | 0.00287035 | missense, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27944931 | TCCCTCATTGAACAC[A/G]ACGCAATCACTGTAG | 55130 |
| rs763616785 | snp | C/T | 3.30033e-05 | 0.00406209 | missense, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983955 | CTCCACGGTGGGGCT[C/T]GACATCCATTTGAAA | 55130 |
| rs763662864 | snp | A/G | 4.96315e-05 | 0.00498129 | missense | ARMC4 | GRCh38.p7 | 10:27935248 | TGGCTTTGTATTCCC[A/G]AAACCTAAGTTCATC | 55130 |
| rs763663184 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27905519 | TACAAAAAACTACTT[C/T]AAATTTCATATGGAA | 55130 |
| rs763664814 | snp | A/C | 6.67401e-05 | 0.00577629 | intron-variant | ARMC4 | GRCh38.p7 | 10:27860588 | CCAGGCTACATTTAC[A/C]AAACTTGGACTAAAC | 55130 |
| rs763690883 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27969590 | TCAAACACCCCAAAA[C/T]TGATGAGAATCAATC | 55130 |
| rs763713463 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27857363 | AACTGTTGATGTTTT[C/T]GGTCAACAGTAGGCT | 55130 |
| rs763716076 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27904218 | TGCAATGTGGTGCAC[A/T]TTCCTAAAGCCTTCC | 55130 |
| rs763720856 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27882819 | TATGGCAATTCCTAG[A/G]AAAAGCACCAATCAC | 55130 |
| rs763728147 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27833286 | GTGTCCCTAAAAATC[-/A]TCAGCAATTTGAAAA | 55130 |
| rs763740936 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27905221 | GGTTATTTTCAGTTC[-/A]AAAAAAAAGAAATGT | 55130 |
| rs763745054 | snp | C/T | 4.30617e-05 | 0.00463993 | synonymous-codon, intron-variant | ARMC4 | GRCh38.p7 | 10:27968961 | TGAAACAGATGGTCT[C/T]GGTTTTTCAAGTTTT | 55130 |
| rs763745513 | in-del | -/ATAA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27911384 | ACTGATTTGGGGGTT[-/ATAA]ATAAAGTTTAGAGAC | 55130 |
| rs763746279 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27939066 | TCTGTTTTCTGGTAT[A/C]CTATGAAATGTATCA | 55130 |
| rs763796430 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27913436 | TGTTCTCCAGCTCTA[A/T]GCATGTTGTTGCAAA | 55130 |
| rs763806311 | snp | C/G | 3.3264e-05 | 0.0040781 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944186 | GTGCAGTGGCGGCTG[C/G]CACTAGATGACGATG | 55130 |
| rs763810586 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27839145 | ACATGATGATGTTAA[A/G]AAAAGGAATAACTCT | 55130 |
| rs763818488 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27953250 | ATGTTGTACAGCAGA[C/T]ATCTGGAACTTATTC | 55130 |
| rs763818965 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27978761 | CACACCACTGCACTT[A/C]AGCCTGAGTGACAGA | 55130 |
| rs763848213 | in-del | -/AATCAGTGGC | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27882908 | GTGTTTGTTATACAA[-/AATCAGTGGC]AATTATTTAACAAAA | 55130 |
| rs763853411 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27817357 | ATTCTTTTCAAAAAT[G/T]TTGGATATATTTCGA | 55130 |
| rs763855258 | snp | A/G | 1.70336e-05 | 0.00291831 | intron-variant | ARMC4 | GRCh38.p7 | 10:27995185 | TAGCACACGCACTAC[A/G]TCAGAGCAGAAAGAG | 55130 |
| rs763861323 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27894997 | ACAGGCATATGGAAA[G/T]ACATACAGAGAGAAT | 55130 |
| rs763864121 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27980089 | AGAGAAAGGACAATC[C/T]CTTCAACAAATTGTG | 55130 |
| rs763869311 | snp | A/C | 1.87362e-05 | 0.00306068 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27944235 | ACCAGTTTGGTGATA[A/C]CCCCGTGCTGCCTCA | 55130 |
| rs763894304 | snp | A/G | 1.64857e-05 | 0.00287099 | missense | ARMC4 | GRCh38.p7 | 10:27935166 | TGGCAGCATTCTCCC[A/G]AGGCCCCAACCACAT | 55130 |
| rs763900795 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27837786 | TGTAAATGAACACAG[C/T]ATCCGCAAGCCCTGA | 55130 |
| rs763935113 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27826158 | CAGAATGGGATCAAG[A/T]ACATCAAGAGGCACT | 55130 |
| rs763943999 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27813412 | AGATAATTGGCTTAA[C/T]GCTTTCTGTCCTTCT | 55130 |
| rs763955023 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27880969 | AAACTACCAGCTTAA[G/T]AGTAAGTCCCATAGT | 55130 |
| rs763993623 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27986450 | AGTTGAATTGAATGA[A/G]TAATCCTTCATCTAT | 55130 |
| rs764030733 | snp | C/T | 1.65888e-05 | 0.00287996 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27862455 | TGCCAGTTTGGACAA[C/T]AAAGGAACAACTCCA | 55130 |
| rs764074122 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27947989 | TTTTTCTCTTCTAGA[C/T]AACTTCCACATCTTT | 55130 |
| rs764079113 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27925775 | GCATCCCCACTAAAA[C/T]TATGAACAAGACAAA | 55130 |
| rs764088128 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27814377 | GCTGTCTCAATGAGA[A/T]TAAATAAGAAAGGAA | 55130 |
| rs764101220 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27980723 | TCTTTGGATAATGCT[G/T]GTGAGAATGAAAATG | 55130 |
| rs764114698 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27836073 | GAAGAGGGGTTGGTC[C/T]TGCTGTCTCAGGGGT | 55130 |
| rs764129979 | snp | C/T | 1.70822e-05 | 0.00292247 | intron-variant | ARMC4 | GRCh38.p7 | 10:27961738 | CAATAACAACACACA[C/T]ACACATGTAAGCTAT | 55130 |
| rs764136103 | in-del | -/CTGT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27835752 | CAACATGGCGAAACA[-/CTGT]CTGTACTAAAAATAC | 55130 |
| rs764160700 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27868600 | AAAACCAAACAACAC[A/G]TGTTCTCACTCATAA | 55130 |
| rs764163028 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27910375 | GCAATTCCAGAGCTC[A/G]GTATTTAAATTTTTT | 55130 |
| rs764180422 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27929356 | TGAAAGATGATAAAA[C/T]TTGCATACTTACACA | 55130 |
| rs764188316 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27915489 | GGCCTCTACCCTCAC[A/G]TCCTAATCACTTCCC | 55130 |
| rs764219226 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27877497 | GTCCCTCTGAAGTTT[A/G]TTTGTTTTGAAGGTG | 55130 |
| rs764226948 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27973827 | CTGGATTAAATGGTA[C/G]TTCTGTTTTTAGCTC | 55130 |
| rs764233304 | snp | C/T | 1.651e-05 | 0.0028731 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27812597 | TCCTGGAGATCCTGG[C/T]CAGGGGACCCAACCA | 55130 |
| rs764249970 | snp | A/T | 1.65318e-05 | 0.002875 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944785 | GAAGGTGGGAACAAG[A/T]CTCCGCATCCAAGGT | 55130 |
| rs764268313 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27952561 | CCCATCCCCTTTCCC[C/T]GACAGGCCCTGGTGT | 55130 |
| rs764269594 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27941829 | TGTCCCTGAAGGTCA[A/T]CTTCCACAGATACTG | 55130 |
| rs764287465 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27923544 | AATTTCATACAGCAG[C/T]TACAGCATAAGACAG | 55130 |
| rs764297273 | snp | A/G/T | 8.76902e-05 | 0.00662109 | intron-variant, utr-variant-3-prime | ARMC4 | GRCh38.p7 | 10:27939877 | AGAACGCCAACAACC[A/G/T]CTGGGAGAGTTCACT | 55130 |
| rs764313201 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27822487 | GGCATTGCAGTGACG[C/T]TGTAGCACTCATGCA | 55130 |
| rs764321789 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27937504 | TGAGTGATATCAATA[G/T]TACCTGACATTTTAT | 55130 |
| rs764326909 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27885549 | ATATATATATATATA[A/T]ATATATAAATATAAA | 55130 |
| rs764328796 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27829284 | TGCTCCTACTAAATC[A/G]GAACTAAACTCATAA | 55130 |
| rs764373840 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27937588 | CAGATGGTCTCAACT[A/G]ATCATTCTTCCCGGG | 55130 |
| rs764374725 | in-del | -/AAG | | | intron-variant, cds-indel | ARMC4 | GRCh38.p7 | 10:27996044 | GAAATTAGTCTGTAA[-/AAG]AAGATCTTTTAAAAA | 55130 |
| rs764380957 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27827692 | TTCTCTCTCCCTGGA[C/T]GACTGCCTAACTCAT | 55130 |
| rs764390216 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27876689 | CTCCTACTTATAGGC[A/T]GGAGTCATCACAGGT | 55130 |
| rs764401607 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27998126 | CACAACCGAATTCTT[C/T]AGGGGGCTACGGAAA | 55130 |
| rs764402372 | in-del | -/T | 0.000115455 | 0.007597 | frameshift-variant | ARMC4 | GRCh38.p7 | 10:27862492 | GTGATAACAGCTAAA[-/T]TTTCTTGATCTTTTG | 55130 |
| rs764404279 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27931606 | AATATGAAAAGAATA[C/T]AGCTGTTTTCTCTGG | 55130 |
| rs764407154 | snp | A/G | 1.65833e-05 | 0.00287948 | intron-variant | ARMC4 | GRCh38.p7 | 10:27907785 | CAATTATCCTATCGT[A/G]GAACCCAAAATCATG | 55130 |
| rs764419268 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27899641 | GGGGAGGGGAGTCTG[C/T]CATTACTGAGGCTTG | 55130 |
| rs764448983 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27844098 | AGCTACTGGGGAGGC[C/T]GAGGCAGACAGACCA | 55130 |
| rs764460220 | snp | A/G | 6.59196e-05 | 0.00574068 | missense, synonymous-codon, intron-variant | ARMC4 | GRCh38.p7 | 10:27812541 | CCTTCTCTGTAGCAA[A/G]AGCCAGCCTGCGGAT | 55130 |
| rs764462367 | snp | C/G | 1.6498e-05 | 0.00287206 | intron-variant | ARMC4 | GRCh38.p7 | 10:27935001 | CTTTCCATCTCCAGG[C/G]CCACTTACATCATAC | 55130 |
| rs764463680 | snp | A/T | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27960909 | ATATCTGACGTCAGA[A/T]ATGAATATTAAGCTG | 55130 |
| rs764467270 | in-del | -/CCGTGCTGCCTCACCACCCG | 1.83488e-05 | 0.00302887 | frameshift-variant, intron-variant | ARMC4 | GRCh38.p7 | 10:27944237 | AGTTTGGTGATACCC[-/CCGTGCTGCCTCACCACCCG]CCGTGCTGCCTCACC | 55130 |
| rs764472845 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27853751 | TAGTATCATAAAAAA[G/T]TTTACTCGAATGGGT | 55130 |
| rs764481133 | snp | A/T | 1.67066e-05 | 0.00289016 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944445 | ATCTGTGTGAGAAAA[A/T]AAAAGATGAGTGGCG | 55130 |
| rs764481366 | snp | C/T | 1.65064e-05 | 0.00287279 | missense | ARMC4 | GRCh38.p7 | 10:27994959 | CTGAGGGCGCCAAAC[C/T]TGTGTTCCATTCAAG | 55130 |
| rs764484363 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27965475 | AAAAAATGTAGAAGA[C/G]AGAGCAAAGTGGAAG | 55130 |
| rs764487158 | snp | A/C | | | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999305 | GAGCAGAAAGGAAGC[A/C]GAAAATATTCCTTAG | 55130 |
| rs764487195 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27851680 | GAGCTGTGGGAAAAC[A/G]TTTACCTATATTTTC | 55130 |
| rs764489423 | snp | A/C | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983369 | CTGTGGGGACCAGCA[A/C]AGCCTGGAAGTGGAC | 55130 |
| rs764492395 | in-del | -/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27848543 | ACAATGGTAACAAAA[-/G]CCAAAATTGACAAAT | 55130 |
| rs764509987 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27932556 | AATGATAAATTCTAT[A/T]TGGAAAATATTTGAA | 55130 |
| rs764513213 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27944083 | AAAATAATTCTTAAG[A/G]GCAAGCGATACAGAC | 55130 |
| rs764528411 | in-del | -/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27963794 | TCATTACCCTTTTTT[-/G]AAGTGAGTTTTTTAG | 55130 |
| rs764552185 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27817206 | TGGTTATCCTAACAC[A/G]TGGCTTACATGTCTT | 55130 |
| rs764555755 | snp | A/T | 7.86519e-05 | 0.00627055 | intron-variant | ARMC4 | GRCh38.p7 | 10:27994877 | TTGATAATACTATGT[A/T]CAACGAAGATATCAA | 55130 |
| rs764565658 | snp | G/T | 1.64825e-05 | 0.00287071 | missense | ARMC4 | GRCh38.p7 | 10:27940694 | TCGTATGACTCTTAC[G/T]GCAGCTCCACAGGGC | 55130 |
| rs764580278 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27839357 | GCTCACACCTGATAA[A/G]CTTTTTACGTAACTC | 55130 |
| rs764627123 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27881182 | TACTGTTTTTTATTA[C/T]TATTTTTAGAAAGTA | 55130 |
| rs764634312 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27995273 | ACTAGTACTCCCCAT[C/T]CCACATTCTGCTTAT | 55130 |
| rs764639336 | in-del | -/AAAA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27882168 | GTGAGACCTTGTCAT[-/AAAA]AAAAAGAAAGAAAGA | 55130 |
| rs764648303 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27888059 | AAAAAGCCTCCCAAC[A/G]AAGAAAAGGACACTT | 55130 |
| rs764649778 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27966675 | CACTTAGGCAAGATG[A/T]GACACAGAGAACCTT | 55130 |
| rs764661844 | snp | A/G | 1.6664e-05 | 0.00288647 | synonymous-codon, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27961615 | AATATTCTGATGGCA[A/G]ATCTGCACTTGCTTC | 55130 |
| rs764662616 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27995259 | TCTCAAGACTTTAAA[C/T]TAGTACTCCCCATCC | 55130 |
| rs764698031 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27940372 | TGAGATATATATATA[C/T]ACATATATGTGTATA | 55130 |
| rs764727831 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27868059 | AAGAAGACATTTATG[C/T]GGCCAACAAACATGA | 55130 |
| rs764745920 | snp | A/G/T | | | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27858066 | CCCTGATGTGCCAAA[A/G/T]TTTTTTGCATTACCT | 55130 |
| rs764745966 | in-del | -/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27878829 | TAAGATCCTTGTTCT[-/G]TTCCCAGTTGTTAAC | 55130 |
| rs764760402 | snp | C/T | 0.000121205 | 0.00778381 | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27958959 | TTTCTGCCATTTTGA[C/T]TTGTTTCCTTTTGCT | 55130 |
| rs764790751 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27941947 | GAGATCCAGTGGGAC[C/T]GGCTTGAGACAGGTG | 55130 |
| rs764795725 | snp | A/G | 1.66646e-05 | 0.00288652 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984335 | AATACTTTAAACAGA[A/G]TCTAGGAAACACATG | 55130 |
| rs764798721 | snp | C/T | 1.64825e-05 | 0.00287071 | missense | ARMC4 | GRCh38.p7 | 10:27860741 | ATTTCAGATAACGCA[C/T]TAGTGGAGCCACTGC | 55130 |
| rs764803759 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27929944 | TCACAGCAAAGTTTT[A/C]TTCTGTTATATCTTT | 55130 |
| rs764805058 | snp | A/T | 1.65356e-05 | 0.00287533 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940556 | GAAGCAGAACTGGCA[A/T]GAGTACCTCTGATGC | 55130 |
| rs764817165 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27965544 | GAGAGTCCAGGAGGA[A/G]ACAGGACTCATTCAA | 55130 |
| rs764871289 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27895216 | TAGCAGATGGCTTAC[A/G]AAAACAACTCTGTCT | 55130 |
| rs764878556 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27998129 | AACCGAATTCTTTAG[A/G]GGGCTACGGAAAGGC | 55130 |
| rs764886603 | snp | C/T | 1.64789e-05 | 0.0028704 | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27936708 | CTTCATTTCAGAATA[C/T]TGAGAGCCTTCTCTT | 55130 |
| rs764896532 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27866233 | GATGGAGCTTTAGTA[G/T]TTGCATGTCATAGAT | 55130 |
| rs764907463 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27827604 | AACTCCTCTTGTTTT[C/T]ACTTGTCAATTATCT | 55130 |
| rs764919777 | snp | A/T | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27960762 | ATCAAGCAAAGCCAC[A/T]GGCAAATGCCCTTGG | 55130 |
| rs764931318 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27929017 | TCCAGAATCCATATG[C/T]TTAGCCATTATACAC | 55130 |
| rs764950964 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27813586 | ATTTTTTTACCCAAT[A/T]GCATTTGAGTGCAAA | 55130 |
| rs764966447 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27980403 | GTTATAAGGCAACCT[C/G]CAGAACAAGAGAAAA | 55130 |
| rs764974307 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27814135 | GAGAAAAATGGAATT[C/T]ATTGGGCAAAATGGG | 55130 |
| rs764991835 | in-del | -/TCTC | | | downstream-variant-500B, intron-variant | ARMC4 | GRCh38.p7 | 10:27811979 | ATGACCTTGGGATGA[-/TCTC]TCTAAGTCCAGCTGC | 55130 |
| rs764996710 | snp | C/T | 1.74543e-05 | 0.00295412 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27944244 | GTGATACCCCCGTGC[C/T]GCCTCACCACCCGCC | 55130 |
| rs765003882 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27882585 | GGCTTGCAACAAACA[A/G]CATCTATTCAAGAAA | 55130 |
| rs765009287 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27962589 | AGGACCAAAGAGTTA[A/G]CCACCAACTCTGAGA | 55130 |
| rs765025001 | snp | A/G | 1.64871e-05 | 0.00287111 | synonymous-codon, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984209 | TTCAATAGATTCCAA[A/G]ACTGTTTGGTTTCCT | 55130 |
| rs765119649 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27987753 | AAGCCTAGTGACCAA[C/T]AGGATATAACCAAGG | 55130 |
| rs765131065 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27883835 | AGGCAGAAGAGACAC[C/T]CAGTGAGCATGATAG | 55130 |
| rs765133742 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27834803 | TTTAATTCTCAGATG[C/T]CCTTGTTTACCAACA | 55130 |
| rs765139592 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27972342 | AAAAAGCTCAATTCA[A/G]AAGGGGCAGAGGAAG | 55130 |
| rs765142074 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27890484 | CACAATTCTATATAT[C/T]CCTGTTTAGAATAGG | 55130 |
| rs765150424 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27852526 | CACTAAATGACAACA[C/T]GGAATAATAACTAAT | 55130 |
| rs765175960 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27952452 | GTGCAGGTTTGTTAC[A/T]TAGGTAAACGTGTGC | 55130 |
| rs765190139 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27948055 | ACATAAATTCATAAC[A/G]GCCATTTAATTGCAG | 55130 |
| rs765193490 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27824362 | CTCTGCCCTTATGAA[C/T]GGATTAATGCTGTTA | 55130 |
| rs765196629 | in-del | -/TGTT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27831830 | CTACTCAATGGAGCC[-/TGTT]TGTTTCTGCAAACCC | 55130 |
| rs765219478 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27833948 | GAGAACATTCCAAGC[C/T]GAGAAAGGACAGCGG | 55130 |
| rs765225796 | snp | G/T | 1.64898e-05 | 0.00287135 | missense, intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27971188 | CCAAAAATTAATTTG[G/T]TTCTTCTCCAGTGAC | 55130 |
| rs765227802 | snp | A/G | 2.88563e-05 | 0.00379833 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944192 | TGGCGGCTGGCACTA[A/G]ATGACGATGACAACA | 55130 |
| rs765240413 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27861143 | ATTACAGGTGCCCGC[C/T]ACCACACCTGGCTAA | 55130 |
| rs765275522 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27902724 | AAATTCCTGGACACA[C/T]ACACCCTCCCAAGTC | 55130 |
| rs765276317 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27935445 | GCTCCAGACCTGCAC[C/T]CTTAATCACCATGCA | 55130 |
| rs765304288 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27998175 | GATCTATGAAATGTG[A/G]TTGGTAACATCCACG | 55130 |
| rs765314452 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27861887 | AGGGTTTGAATTTCT[A/G]CTCTATGACTTTTCT | 55130 |
| rs765319386 | snp | C/T | 8.01828e-05 | 0.00633127 | intron-variant | ARMC4 | GRCh38.p7 | 10:27969021 | TGCTGAGCCTTTGCT[C/T]TAAAAAAATATACAA | 55130 |
| rs765340611 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27932636 | CATGTTGGCTACTCC[G/T]GTCTGATATGTTCAT | 55130 |
| rs765367670 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27878716 | CGGGCAAATCTTGTC[A/G]TCAAAAGTATACTTA | 55130 |
| rs765368834 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27958167 | TCCAAGCAATTTACT[C/G]TCTGGCCAAGAGTAT | 55130 |
| rs765375928 | snp | A/C | 1.65165e-05 | 0.00287367 | missense | ARMC4 | GRCh38.p7 | 10:27987404 | CAACACATGCTTGGG[A/C]TTCCTTCAACTTCCC | 55130 |
| rs765376402 | snp | A/G | 1.64963e-05 | 0.00287192 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27862512 | TTGATCTTTTGCTAT[A/G]TTGGTAATGGCAGCA | 55130 |
| rs765376459 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27911580 | GAAGACACCAGTTTA[C/T]TCACAGGCCACAGAG | 55130 |
| rs765376476 | snp | C/T | 1.67167e-05 | 0.00289103 | missense | ARMC4 | GRCh38.p7 | 10:27940007 | CAGCCCGGTAGTTTT[C/T]CTAGGAATAAAAACC | 55130 |
| rs765407832 | snp | C/T | | | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999344 | TTTTACATTTTTCCA[C/T]AGGCTTCCAGACAAG | 55130 |
| rs765417086 | in-del | -/TT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27988339 | ACACCTGATCTAGCT[-/TT]TTTTTTTTTTTTTTT | 55130 |
| rs765428794 | snp | C/T | 3.36973e-05 | 0.00410457 | missense | ARMC4 | GRCh38.p7 | 10:27862616 | AACGAACCATTTCCC[C/T]AGCATCCTAGACAAA | 55130 |
| rs765431008 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27927301 | TGACCCAAGTTTTTA[C/T]CATAGCCACAGCCAA | 55130 |
| rs765435884 | snp | C/T | 3.29576e-05 | 0.00405928 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27944888 | ATCTCTGATGGCCAA[C/T]TGGCAGGTTTCTTGA | 55130 |
| rs765458644 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27944497 | TTTTAAAAATTCCGA[A/G]TATACCTAAAATCCT | 55130 |
| rs765472215 | snp | A/G | 1.68403e-05 | 0.0029017 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944451 | GTGAGAAAAAAAAAG[A/G]TGAGTGGCGAATATG | 55130 |
| rs765478393 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27817330 | CCTCACTTTACTGTA[C/T]AGACAGTTAAAATTC | 55130 |
| rs765532440 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984463 | TCAAGTAATTAGTGA[C/T]TTATGTTTAATGCAA | 55130 |
| rs765554199 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27888207 | CAGATCAAATGGTAG[C/T]TCTATTTTTAGTTCT | 55130 |
| rs765557199 | snp | A/C | 3.32989e-05 | 0.00408024 | intron-variant | ARMC4 | GRCh38.p7 | 10:27812630 | TCCAGTAGAAGCTGT[A/C]ACACATAAGGAGGAG | 55130 |
| rs765557827 | in-del | -/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27870707 | TTTTATGGCTGCATA[-/G]TATTACATGATGTAT | 55130 |
| rs765572557 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27919454 | GTTCAAAATATGTAA[C/T]AGACTTCAACAAAAG | 55130 |
| rs765588641 | snp | G/T | 1.69347e-05 | 0.00290982 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983824 | CTGGCTTTAGTTACG[G/T]TTTTAAAAATTTACT | 55130 |
| rs765595294 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27988301 | TACAGGAGGCTATAT[C/T]TGATGAAACTCCTGA | 55130 |
| rs765611160 | snp | C/T | 1.66693e-05 | 0.00288693 | missense | ARMC4 | GRCh38.p7 | 10:27939908 | GCACCTGGTAAATGG[C/T]CATGGCGCAGTGCTC | 55130 |
| rs765612657 | snp | A/C | 0.00246406 | 0.0350137 | intron-variant | ARMC4 | GRCh38.p7 | 10:27853407 | AAAAGTAAGCCCTAA[A/C]TATATGCTGCCTACT | 55130 |
| rs765615630 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27889231 | GATCAAGTTGGACCC[A/G]ACCTTCTGACCAGAA | 55130 |
| rs765619120 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27844189 | AACAGAGCAAGACCC[C/T]GTCTCAAACCAAAAA | 55130 |
| rs765631471 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27900689 | TACCAATAGCTGAAT[C/T]GATCAGGCGGAAGAA | 55130 |
| rs765640205 | snp | C/T | 1.65192e-05 | 0.00287391 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944791 | GGGAACAAGACTCCG[C/T]ATCCAAGGTGACAGA | 55130 |
| rs765654379 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27991024 | ATCCAATTTATAAAT[C/T]TCCCAAGCTACATTA | 55130 |
| rs765656045 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27832228 | CCTTGAATAATTCTC[C/T]GGTACACAATGAAAC | 55130 |
| rs765679963 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27918740 | AAGGATTGTGGGGGG[-/A]AGTGAACTGTCATTA | 55130 |
| rs765707922 | snp | C/T | 1.65157e-05 | 0.0028736 | missense, utr-variant-5-prime, intron-variant | ARMC4 | GRCh38.p7 | 10:27981548 | ATTGAACCTTTTCTC[C/T]CATAATTAACGTCCC | 55130 |
| rs765720743 | snp | C/T | 1.64939e-05 | 0.0028717 | missense | ARMC4 | GRCh38.p7 | 10:27994980 | TCCATTCAAGTGGTT[C/T]CACAAAAACAAATTT | 55130 |
| rs765722458 | snp | A/C | 3.29728e-05 | 0.00406021 | stop-gained | ARMC4 | GRCh38.p7 | 10:27935026 | TCATACTTTCAGGTT[A/C]TACTGCACAAGCACC | 55130 |
| rs765735015 | in-del | -/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27912713 | AGTGGCTCAAACTAA[-/G]TGTGGTTTGCTTAAA | 55130 |
| rs765755812 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27965653 | TCTGGCTTCCCATTA[A/G]TCTTTACAAAATGTA | 55130 |
| rs765762038 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27985992 | AGATGAAAATATGTA[C/T]GCATTGAGATGGGGG | 55130 |
| rs765777908 | snp | A/T | 1.65121e-05 | 0.00287329 | missense | ARMC4 | GRCh38.p7 | 10:27995109 | CATGTCCGGCAGCAG[A/T]CCACTGCGTCAATTT | 55130 |
| rs765803814 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27915058 | ATCTTCCCCCAAATT[A/G]ATGGCAGACATTAAT | 55130 |
| rs765811989 | snp | C/T | 1.65329e-05 | 0.0028751 | missense | ARMC4 | GRCh38.p7 | 10:27940793 | AATCATGTGCACAGT[C/T]TAGTAGAGCAACCTA | 55130 |
| rs765814597 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27902884 | ACAAAGAGGAGCTGG[C/G]ACCATTCCTTCTGAA | 55130 |
| rs765838753 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27897666 | CACTTTCTTGTTGAC[A/G]ATTCTTCAAATGTTC | 55130 |
| rs765857367 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27930073 | TTAACATTTTATATA[C/T]TTTTATTTTTTATTT | 55130 |
| rs765903108 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27928790 | TGAACCTATTTCTAC[A/C]GCAACAATACTAGCC | 55130 |
| rs765937444 | snp | C/G/T | 1.70403e-05 | 0.00291888 | synonymous-codon, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27961715 | CTTTTCAGCACTCTT[C/G/T]CTAAGAACAATAACA | 55130 |
| rs765957006 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27814528 | TCCACCTTCAGAGTT[A/G]CATCTGGGCCCTGAT | 55130 |
| rs765958428 | snp | G/T | 1.66161e-05 | 0.00288232 | missense | ARMC4 | GRCh38.p7 | 10:27860840 | GATGTCTCAATTTAT[G/T]GTTATTCTGTGCAAG | 55130 |
| rs765961959 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27964515 | CTGCTGGCTGCCAGG[-/T]TATCAAGTGAATGCT | 55130 |
| rs765989947 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27916342 | GAACAAGCACAGGGT[A/G]AAGAGAGCATCTGCA | 55130 |
| rs766001945 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27836086 | TCTTGCTGTCTCAGG[C/G]GTGGCAGAGTCAGAA | 55130 |
| rs766018899 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27989307 | CTATCACCAGCACTT[C/T]AGATAGGAACTGCAC | 55130 |
| rs766021060 | in-del | -/TTTA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27838750 | AGGAGCAGCATATAC[-/TTTA]TTTTACCATACTGTT | 55130 |
| rs766022265 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27882714 | GCAACCTTGCAACCG[C/T]GGAATCTGGGGAAAT | 55130 |
| rs766066471 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27926154 | CTTTGCAGTTGTAGC[A/C]CAAATGCAGCCAAAG | 55130 |
| rs766070495 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27828985 | GGGCACATTATTAGA[A/G]GAAATTCGAAACCAA | 55130 |
| rs766073096 | in-del | -/TAAG | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27854881 | GAATTAATACGAAAA[-/TAAG]TAAGCTGAGTGAAGG | 55130 |
| rs766089550 | in-del | -/GCCC | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27955904 | CTTCTGAAGCTGGCA[-/GCCC]GCCCGGTGGCATTTC | 55130 |
| rs766131259 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27950530 | CAAGCTGCTAAGAAT[C/G]TTTTATCAGGAATGG | 55130 |
| rs766131481 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27835024 | ACAGAACACACAACC[A/G]AAGGCGCAGGGGTTG | 55130 |
| rs766132314 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27892018 | CTTCATAATACTGAA[C/T]ACCTGTTCAACTACC | 55130 |
| rs766142892 | in-del | -/AAT | 0.00241643 | 0.0346753 | intron-variant | ARMC4 | GRCh38.p7 | 10:27853395 | AATAAATAAATAAAA[-/AAT]GTAAGCCCTAACTAT | 55130 |
| rs766183879 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27903253 | AAAATTCAACACTCA[C/T]TCATGCTAAAAACTC | 55130 |
| rs766209589 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27947774 | GACATGGAACAGTGT[A/G]TCATACCTTGTTTAA | 55130 |
| rs766213333 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27892291 | GTTCAAATAAAACTT[C/T]TTTAAAAATATGCAG | 55130 |
| rs766217891 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27852646 | GGAAAAATAGAAAAC[A/G]AATAACAAGATGGTA | 55130 |
| rs766237759 | snp | C/G | 1.64846e-05 | 0.0028709 | missense, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984247 | AGAAACGTTTGAGCA[C/G]TTCTATATCCTTCTT | 55130 |
| rs766245314 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27839856 | AAACTCAGGTTGACA[A/G]TATAATAGTACACCT | 55130 |
| rs766249560 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27974230 | ATTCTGTAGATTGTC[C/T]GTTTATTCTGTTGAC | 55130 |
| rs766284471 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27836161 | GTTCAAGGGTCAACT[A/G]TATATATATTCAGTA | 55130 |
| rs766288309 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27877655 | AAACTGTCTTTCACC[A/G]ATGCTGAACGACTGG | 55130 |
| rs766293226 | snp | C/T | 4.6277e-05 | 0.00481003 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984986 | GCAATCTTGGCTCAA[C/T]ACAATAGAGGTTCCT | 55130 |
| rs766307918 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27976355 | ATATCTACATAGAAA[A/C]CCCTCTGGAATGTAT | 55130 |
| rs766325415 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27848959 | ACTGTTAGTGGGACT[A/G]TAAACTAGTTCAACC | 55130 |
| rs766361375 | snp | A/G | 3.32392e-05 | 0.00407658 | intron-variant | ARMC4 | GRCh38.p7 | 10:27935271 | AGTTCATCATAAGAA[A/G]GAGGAGAATTGGTTT | 55130 |
| rs766362872 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27991108 | TGGTGTCATTTGTTC[C/T]TAGTTTACAGCAAAT | 55130 |
| rs766372369 | snp | C/G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27934115 | TCTCTTCTCTATTCC[C/G/T]TGCCACCATGTAAGA | 55130 |
| rs766383476 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27908969 | GTAAGTAGGTTTTCA[A/G]ACCTAAAACTTTCAT | 55130 |
| rs766408346 | in-del | -/AGGAGAA | 1.65012e-05 | 0.00287234 | frameshift-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983974 | TCCATTTGAAAATTC[-/AGGAGAA]ATAATCTGAAACCAA | 55130 |
| rs766451732 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27960246 | TCTCCAAGTTGAGCA[C/T]TAGGGCTTGTTTCGT | 55130 |
| rs766455172 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27888330 | CCAACATACATTGTT[C/T]TTGTTTGTTTTACTT | 55130 |
| rs766485421 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27874372 | TTAAGGTTAATATTG[C/T]TATGTGTGATTTGAT | 55130 |
| rs766491818 | snp | A/T | 1.82533e-05 | 0.00302098 | synonymous-codon, intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27971311 | TTCACTGAAGCTAAT[A/T]CCCTTTATTTAAAAA | 55130 |
| rs766494093 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27863437 | ACGTGTGCATTGGAC[A/G]ACTCAAATTTTTCAC | 55130 |
| rs766495166 | in-del | -/A | 0.000608327 | 0.0174297 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944441 | ACCAATCTGTGTGAG[-/A]AAAAAAAAGATGAGT | 55130 |
| rs766509534 | in-del | -/AC | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27939140 | AGATAAAACAGGAAC[-/AC]ACACACACACACACA | 55130 |
| rs766528273 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27986190 | GGAATCAACCATTTA[C/T]TGAGCATCTCAACTT | 55130 |
| rs766533179 | in-del | -/TAG | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27867113 | GGACAATATACACCA[-/TAG]TAGGTGAACAAGATA | 55130 |
| rs766548033 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27920765 | AGACATATCTGGGCA[A/G]CCACAGAGAGATTAA | 55130 |
| rs766552554 | snp | A/G | 1.65031e-05 | 0.00287251 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27987420 | TTCCTTCAACTTCCC[A/G]GTTTTGGCAATAAGT | 55130 |
| rs766568853 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27889351 | ACAGTCTGCCTGAAA[C/G]AAGATGAAAGAAGAG | 55130 |
| rs766590684 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27913153 | CAACTTTTTAGTTTT[A/G]GGGGTACATGTGCAG | 55130 |
| rs766599376 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27933831 | CTTGTATTCCTTAGT[A/G]TCTGAAACACTGGAG | 55130 |
| rs766628611 | in-del | -/TGTC | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27930827 | ACACTGAGAACACGT[-/TGTC]TGTCATTTAGTTTTG | 55130 |
| rs766670823 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27858303 | GGGGCTCAGAACAGA[A/G]TAGGAAGAAGAGGTC | 55130 |
| rs766678622 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27833163 | ACATATTTAGAGGTG[A/C]CTCTGGGATGCATTC | 55130 |
| rs766681902 | snp | A/G | 1.69556e-05 | 0.00291162 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27862620 | AACCATTTCCCCAGC[A/G]TCCTAGACAAAAATA | 55130 |
| rs766707493 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27911774 | CTCATACCACATTAC[-/T]TTGCCTTGTAGTCTT | 55130 |
| rs766742672 | snp | A/C/T | 3.3501e-05 | 0.00409262 | intron-variant | ARMC4 | GRCh38.p7 | 10:27860578 | AAGTTTCTTTCCAGG[A/C/T]TACATTTACCAAACT | 55130 |
| rs766765094 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27831329 | AAACGACATTCCCCT[C/G]CCCAAATCCACCGTT | 55130 |
| rs766773472 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27996951 | TTCTTTCATTTTACA[A/G]TTAGCACACTATCAA | 55130 |
| rs766779793 | snp | A/G | 3.3849e-05 | 0.0041138 | utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27995178 | CTGAGCTTAGCACAC[A/G]CACTACATCAGAGCA | 55130 |
| rs766781029 | in-del | -/GGATTTAT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27985269 | TGTCTTCTAGTACAA[-/GGATTTAT]CAAACATTAAGACTA | 55130 |
| rs766803159 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27819364 | AGGCAACTCTGGGGT[A/G]AGAGAGATATACTAT | 55130 |
| rs766846723 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27980642 | CTTCACACTGACTAC[A/G]ATGTTTATAATTAAA | 55130 |
| rs766848306 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27841306 | AATCTCTCATCCAAT[A/C]TGTAACTAAGCCACC | 55130 |
| rs766851765 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27896701 | GTGAGAGCCAGGCCT[A/G]TCTTTTTTTCTCCAT | 55130 |
| rs766883310 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27974145 | TTTGTTTTTCTCTTG[-/A]AAATCCATTCTTTAT | 55130 |
| rs766901849 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27995457 | AGAGGATTCAAACAG[A/T]TAGGCATAAAACCCA | 55130 |
| rs766938350 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27859647 | AAGCAGTAAAATTAT[A/G]TTGTACAAGGAAACA | 55130 |
| rs766939772 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27886582 | AAAATATAAAGTTCT[C/T]TGGTAAAAATAAATA | 55130 |
| rs766968993 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27815803 | TCAAATGGCATTCAT[A/T]TGGAACCATCTTCTA | 55130 |
| rs766969083 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27830797 | ACTGATCTTACTTTA[A/G]TATCAGTTTGGATCT | 55130 |
| rs767014342 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27949691 | TTATTTCAAGATTGG[C/T]CAATGTAATTTACAA | 55130 |
| rs767047592 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27918615 | TGGTGAAAAATTGAA[C/T]GCTTTCTCCCCAAGA | 55130 |
| rs767057835 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27922737 | ATGTTGAAACCCTGT[C/T]TCTACTAAAAATACA | 55130 |
| rs767067508 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27964523 | CTGCCAGGTATCAAG[G/T]GAATGCTATTGAAGA | 55130 |
| rs767086472 | snp | A/G/T | 3.39284e-05 | 0.00411865 | intron-variant | ARMC4 | GRCh38.p7 | 10:27812651 | TAAGGAGGAGAAGAA[A/G/T]GGACACAAGAATAAA | 55130 |
| rs767105944 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27947226 | ATAAACCCCCATATT[C/T]GGGTGCAGGAGGCTC | 55130 |
| rs767110877 | snp | A/G/T | 5.16009e-05 | 0.00507915 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944182 | CTGTGTGCAGTGGCG[A/G/T]CTGGCACTAGATGAC | 55130 |
| rs767114873 | snp | C/T | 1.64838e-05 | 0.00287083 | missense | ARMC4 | GRCh38.p7 | 10:27935062 | CTTTTGTAACATTCA[C/T]AAGAAGAGCTTGGTT | 55130 |
| rs767127150 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27991278 | CACCCCAAAATTAAA[C/T]GTGGAAAGATGATGA | 55130 |
| rs767141368 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27867035 | ATGATAGTGGCAAAG[C/T]GTTTGAATCTCATTC | 55130 |
| rs767144194 | in-del | -/GTAT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27833547 | AGAAAAATATTGTAA[-/GTAT]GTATCTCTCCTCAAA | 55130 |
| rs767159063 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27950655 | GCAACGGTGTGATCT[C/T]GGCTCACTGCAACCT | 55130 |
| rs767169905 | snp | A/C/T | 0.00016483 | 0.00907688 | missense | ARMC4 | GRCh38.p7 | 10:27935158 | CACGTTCTTGGCAGC[A/C/T]TTCTCCCAAGGCCCC | 55130 |
| rs767173014 | snp | A/G | 9.06639e-05 | 0.00673229 | missense, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27985073 | TCCAATTGCTTAAGC[A/G]GCATAGCAATCTTCA | 55130 |
| rs767201591 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27927467 | TAAATCTAGCAATAA[A/T]AGCCATGCCTGAAAC | 55130 |
| rs767220064 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27992250 | AACATCAAAGATATC[A/C]ATAACGGTCAGACAC | 55130 |
| rs767254967 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27938753 | TACAGGCACATGCAA[C/G]CACACCCAGCTATTT | 55130 |
| rs767258037 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27836253 | TTTCCTATAACTCTT[C/T]GAGGAAAATATTATC | 55130 |
| rs767271748 | snp | C/T | 1.66504e-05 | 0.0028853 | missense | ARMC4 | GRCh38.p7 | 10:27860845 | CTCAATTTATTGTTA[C/T]TCTGTGCAAGGGAAA | 55130 |
| rs767279846 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27879232 | TCCATTTATGAGGAG[G/T]TCTAAATTGTGAGGT | 55130 |
| rs767279948 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27894672 | GCCTCAACCTCCCAG[G/T]CTCAAGCAATCCTCC | 55130 |
| rs767301278 | snp | G/T | 1.66488e-05 | 0.00288515 | missense, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27961648 | GACGATGGTCAGGTG[G/T]TTCTTCATCTTCCTC | 55130 |
| rs767311449 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27884102 | ATGTAGAATATACTC[-/A]AAAGAGATCCCCAGT | 55130 |
| rs767324976 | snp | A/G | 1.6896e-05 | 0.0029065 | missense | ARMC4 | GRCh38.p7 | 10:27862435 | GATGTGTTACTTACT[A/G]TATTTGCCAGTTTGG | 55130 |
| rs767343695 | snp | A/G | 1.66443e-05 | 0.00288477 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940808 | CTAGTAGAGCAACCT[A/G]TAATAATAGATAAAT | 55130 |
| rs767354789 | snp | C/T | | | utr-variant-3-prime, intron-variant | ARMC4 | GRCh38.p7 | 10:27812261 | ATATTCTCATATTCT[C/T]AGAAACTTATCACAG | 55130 |
| rs767360204 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27887517 | CCCACCTAACAACAG[C/T]AGAATACTCATTTTT | 55130 |
| rs767385199 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27925930 | AGAATTGCTTGAGCC[C/T]GGGATGCAAGGGTTG | 55130 |
| rs767422303 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27862047 | AAGAATGCCATCGAC[G/T]GAAGCTTGCTAAACT | 55130 |
| rs767428927 | snp | C/T | | | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999543 | TGAAATGAAAACATG[C/T]CCCCCATCTCTTTTT | 55130 |
| rs767444245 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27959347 | CACCTCAGAGAGAGT[A/G]GTGTTGGCAAAGTTC | 55130 |
| rs767489618 | snp | C/G | 1.64817e-05 | 0.00287064 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27812534 | TATCTTGCCTTCTCT[C/G]TAGCAAGAGCCAGCC | 55130 |
| rs767497058 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27911616 | CCCCGTTATGCACTT[C/T]CAACTATTGCTGTTT | 55130 |
| rs767502160 | snp | A/G | 4.94311e-05 | 0.00497123 | synonymous-codon, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27936749 | ATTCTCTTTGCTGAT[A/G]GAACATTTCCATATA | 55130 |
| rs767512330 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27897373 | GAAGGCAACTCCATC[A/G]TCTTTTCCTCAGACG | 55130 |
| rs767521263 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27871632 | TTTCCCCATTTCCTA[A/T]TTTTGTCAGGTTTGT | 55130 |
| rs767536392 | snp | C/T | 2.30747e-05 | 0.00339659 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984997 | TCAATACAATAGAGG[C/T]TCCTTTTTGAAAAAG | 55130 |
| rs767552721 | snp | A/G | 4.94833e-05 | 0.00497385 | synonymous-codon, utr-variant-3-prime | ARMC4 | GRCh38.p7 | 10:27936839 | GGGCTTAAGTCCTCC[A/G]TGCAGCCTAACGAGG | 55130 |
| rs767565321 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27923319 | CAAGATATATCAAGC[A/G]AATGGAAACAGTAAG | 55130 |
| rs767572435 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27978490 | ACAAAATGATGGGTG[C/T]ACCAAGAAAAGGAAA | 55130 |
| rs767611586 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27905716 | GAAATAATGCCACAC[A/G]TCTACAACCATCTGA | 55130 |
| rs767636563 | snp | C/T | 3.30393e-05 | 0.0040643 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27944414 | ACTGATTTCCTTCAG[C/T]ATTTTTAATGAACCA | 55130 |
| rs767649423 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27834610 | AAGGAGTGAGATAAC[G/T]ATGGAGAGGCAGGCA | 55130 |
| rs767652411 | snp | C/T | 6.67434e-05 | 0.00577644 | synonymous-codon, utr-variant-5-prime, intron-variant | ARMC4 | GRCh38.p7 | 10:27981496 | TTCTGAAAATTTTGG[C/T]GATTTTTCTCTTAAA | 55130 |
| rs767669816 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27918552 | AGAAGGAAACTTTTT[C/T]AATCTGATAAAACAT | 55130 |
| rs767674897 | in-del | -/AAT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27928796 | TATTTCTACCGCAAC[-/AAT]ACTAGCCTACATTTA | 55130 |
| rs767738420 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27889435 | TCCTAAGCACAGATA[C/T]AATCATCGTAAGTGA | 55130 |
| rs767751007 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27973733 | GCTACTGCGAATAGT[C/G]CTGCAATGAACATAT | 55130 |
| rs767795688 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27819518 | CCAAGGCAGGAGGAT[A/G]GCTTGAAGCCAGAAG | 55130 |
| rs767799478 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27923290 | TGATTCAGAAAGACT[-/A]AAAAAGTGTAGATCA | 55130 |
| rs767834916 | snp | A/C | 2.32523e-05 | 0.00340963 | intron-variant | ARMC4 | GRCh38.p7 | 10:27987557 | CACTAAAAAATAAAA[A/C]TAAAAAATTGAAAGC | 55130 |
| rs767838580 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27897795 | ACAAGAAGAGGGCTG[C/G]AGGCAGGGAGTATTC | 55130 |
| rs767850536 | snp | A/C | 1.65471e-05 | 0.00287633 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940554 | GGGAAGCAGAACTGG[A/C]ATGAGTACCTCTGAT | 55130 |
| rs767876141 | in-del | -/AAAG | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27931124 | TGCTCTCTTAAAAAA[-/AAAG]AAAGAAAGAAAGAAA | 55130 |
| rs767891186 | snp | C/G | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983216 | ATCACTATCAGTCAT[C/G]CAGTGCTCCATTTTC | 55130 |
| rs767895359 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27908553 | AACATGGCTTTGTTT[C/T]GGAAAGGTATATTAA | 55130 |
| rs767913800 | in-del | -/T | 0.000188052 | 0.00969487 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983814 | TCAAAGTCCACTGGC[-/T]TTAGTTACGTTTTTA | 55130 |
| rs767918417 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27876083 | CCACTGCAGCTCAAG[A/G]ATGCCTGCCTGTCAC | 55130 |
| rs767943881 | snp | C/G | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997917 | TTTAAAGATTAAAAG[C/G]AAAAAAGTTTTGGTT | 55130 |
| rs767949599 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27887321 | TACAAACATACATGC[A/C]CCAAACATGAAAGTT | 55130 |
| rs767951327 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27828049 | CAGTGAAAGGCAACA[C/T]TTTAAGGAAATGGGG | 55130 |
| rs767952112 | in-del | -/A | | | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27958936 | TCTGCTTCCTGATCC[-/A]TCTTTTGTTTCTGCC | 55130 |
| rs767959794 | snp | G/T | 0.000198738 | 0.00996642 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27907675 | TACCTTTGCATTTTT[G/T]ATGCATGGACAGAGT | 55130 |
| rs768002030 | in-del | -/T | 1.65222e-05 | 0.00287417 | frameshift-variant, intron-variant | ARMC4 | GRCh38.p7 | 10:27944415 | TGATTTCCTTCAGTA[-/T]TTTTTAATGAACCAA | 55130 |
| rs768019654 | in-del | -/AT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27917985 | GAATTGAAAATCTAC[-/AT]AGTGCCATATCTTTA | 55130 |
| rs768057630 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27942134 | GTGCTCAGAAAGCCC[A/G]TAGCATTTGTGACTG | 55130 |
| rs768067364 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27898915 | TCCAAACACACATTA[C/T]AATTCGCTTTTTAAA | 55130 |
| rs768086264 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27965321 | ACACAGAGCCTAGGG[-/A]AAAGAAGATCTGAAG | 55130 |
| rs768086858 | snp | G/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27982022 | CTGTTCTTCTGTCTG[G/T]GGCATGGTTGCTATA | 55130 |
| rs768101717 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27822766 | AGGGGCTTGCCTTTA[C/T]TGGTGTCTGTCCTCC | 55130 |
| rs768127677 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27859481 | TAAGAGTACTATTCC[-/T]CCTAAGATGTTTCAT | 55130 |
| rs768129501 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27884133 | TAGGCACATCACAGT[A/G]AAACTATTGAAAGAC | 55130 |
| rs768145133 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27975246 | TAGATTAAATTAAAC[A/G]TATTGTAACATTTTT | 55130 |
| rs768154690 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27954869 | AGTAACACACATTAC[C/T]AGTAATCCAAATACT | 55130 |
| rs768165449 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27889194 | TGTGGCTGCTTCTTA[C/T]ATGAAGCTGTGTGCC | 55130 |
| rs768168417 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27870743 | CCACATTTTCTTAAT[A/C]CACTCTATCATTGAT | 55130 |
| rs768176922 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27820202 | CACCAATGGCCCAGG[C/G]TCCACATGCCACTGG | 55130 |
| rs768182225 | in-del | -/AT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27935843 | CACATATGTATGCAT[-/AT]ATATATATATACACA | 55130 |
| rs768203949 | snp | A/G | 4.95749e-05 | 0.00497845 | utr-variant-3-prime, intron-variant | ARMC4 | GRCh38.p7 | 10:27812481 | TCCTGTGTCATGTAG[A/G]ATTTGATAGCTTGTA | 55130 |
| rs768238195 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27934232 | ATAATTACCCAGTTT[C/T]GGGTATGTCTTTATC | 55130 |
| rs768251998 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27921591 | ATATCTATATGCATA[C/T]ATAAATGGATTTTTT | 55130 |
| rs768278806 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27970026 | CAAGAGAATCGCTTG[A/C]ACCTGGGAGGCAGAG | 55130 |
| rs768350560 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27819426 | ATGATTGTACTCTCT[A/G]TCTTCGAGAGAGTAA | 55130 |
| rs768358624 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27818995 | ACCCAACCTTCTCAT[A/G]TGTGTAAAGGGATCA | 55130 |
| rs768359599 | snp | C/G/T | 3.30449e-05 | 0.00406467 | synonymous-codon, intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27971260 | TTCTTCCTTCTTGGG[C/G/T]GCTTTGCCAAGCTGA | 55130 |
| rs768408768 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27953703 | AATAGTAGGATTTCA[-/T]TTATGTATATAAATT | 55130 |
| rs768424462 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27986554 | CATAAAAAGAGGTTG[C/G]CATCCTGAGGTTAGC | 55130 |
| rs768437106 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27942676 | ATGATAATCATAGTA[A/G]TAATTAAATTTTCTG | 55130 |
| rs768438930 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27982751 | GAATTTTGTTTCTGA[A/G]TTCCAAATTTATGTT | 55130 |
| rs768439048 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27929865 | TTATCAGGATATGTG[A/T]TGCTGTTGGTCTTTT | 55130 |
| rs768445383 | snp | C/T | 1.66527e-05 | 0.00288549 | missense | ARMC4 | GRCh38.p7 | 10:27987512 | AAGGCTGTCCATTTT[C/T]ATCAACTTCTTCTGA | 55130 |
| rs768447289 | snp | C/T | 1.64887e-05 | 0.00287125 | stop-gained, intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27971174 | GTCATTTGATTCCTC[C/T]AAAAATTAATTTGGT | 55130 |
| rs768448549 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27897250 | ACCTACACTCAGACC[G/T]CCACTACCTCCTAAA | 55130 |
| rs768457416 | in-del | -/TTT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27820779 | GAAGCCCAGCAACTT[-/TTT]TTTTTTTTTTTTTTT | 55130 |
| rs768460091 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27936026 | AAGATAAAAGTTCCA[C/T]TAGCCGAGGTTACTT | 55130 |
| rs768463119 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27884657 | AAGCAAGGGTAGATA[C/T]TGTGGCCTAGGAAAA | 55130 |
| rs768476917 | in-del | -/C | 1.64844e-05 | 0.00287087 | frameshift-variant, utr-variant-3-prime | ARMC4 | GRCh38.p7 | 10:27936816 | GTGTTATTGAGTAGA[-/C]TGGCCAAGGGCTTAA | 55130 |
| rs768481022 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27959323 | CCAATGGCCCTGTCT[A/G]GAGCTGCCCACCTCA | 55130 |
| rs768490426 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27941848 | CCACAGATACTGCCC[A/G]TAACCACCAATCTCA | 55130 |
| rs768546750 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27956200 | TACCAATGTAACCCC[A/T]TTGTCACTGTTTTCT | 55130 |
| rs768564584 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27865775 | GGTTACAACAAACCA[A/G]ACTAAACTCCTACTA | 55130 |
| rs768565973 | snp | C/T | 3.34275e-05 | 0.00408811 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940522 | TTGGACTAAAGAAAG[C/T]CAAGTTGAGAAGGCA | 55130 |
| rs768567593 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27892694 | CATTTGTTTTATGCA[C/T]TTAATAACAAAATAA | 55130 |
| rs768574335 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27908197 | TTGACTTACCTTACC[A/G]TATGACATATTTTAA | 55130 |
| rs768575978 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27855644 | TAACAGTATTTTTTT[G/T]TCCCTGTGCTAGGCT | 55130 |
| rs768646396 | in-del | -/AAAC | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27922930 | AACAAAATAAAACAA[-/AAAC]AAACAAACAAACAAA | 55130 |
| rs768653075 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27981698 | CGAAGGATCTATATG[A/G]TAGTTTTAATACAGG | 55130 |
| rs768658226 | snp | C/T | 3.29739e-05 | 0.00406028 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944972 | TCCTCCCTACAAAGA[C/T]GCAATGCCAGAGAAA | 55130 |
| rs768675248 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27883423 | AGGCCACGGGAAGGG[C/G]AGAGTCTGACTTCTA | 55130 |
| rs768686259 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27990730 | CTTTCATGATATCGA[C/T]CACAAAGCTAAGGTC | 55130 |
| rs768701372 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27904727 | TTTCCCTGGCTATTC[C/T]GACATGTTTATTTTC | 55130 |
| rs768707558 | snp | A/G | 0.00050226 | 0.0158391 | intron-variant, missense | ARMC4 | GRCh38.p7 | 10:27853317 | GGTTGCAGTGAGCCA[A/G]GATCGTTGTCACTGC | 55130 |
| rs768709172 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27828663 | AGCAATAAAAGATAT[A/G]CACCATTTATTAGAA | 55130 |
| rs768717218 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27832449 | TAGCTGACTACTTTC[C/T]CTCTTGTCCCTTGTA | 55130 |
| rs768719701 | snp | C/T | 0.000115543 | 0.00759988 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27935222 | TGTTAGAAGTCCCAC[C/T]AAGGTTTCAATGGCT | 55130 |
| rs768725675 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27827276 | TCTATACACCCTCCA[A/G]AGGAAATGTCATTCA | 55130 |
| rs768754330 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27894870 | TTGCCCGGCTTCAAA[-/T]GAAATTTTTGTTTCA | 55130 |
| rs768774922 | snp | C/T | 3.29886e-05 | 0.00406118 | missense | ARMC4 | GRCh38.p7 | 10:27860635 | TGTACCTTTACTGCA[C/T]CATTCTCATGCATGG | 55130 |
| rs768809229 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27830718 | GAGTGGATTGTATCT[C/T]TAAGCCTTTTCCAGG | 55130 |
| rs768852245 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27938419 | GCAGCCGTCTACAAG[C/T]TGAGGAGAGAGGCCT | 55130 |
| rs768873917 | snp | C/T | 0.000504414 | 0.015873 | intron-variant | ARMC4 | GRCh38.p7 | 10:27968911 | AACTCGTCTTGCTGA[C/T]CAGAAACATACCGAA | 55130 |
| rs768879426 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27975782 | AAATTGAAGAGAAGA[C/T]GAAACTTTCTAAATC | 55130 |
| rs768889152 | snp | C/T | 1.64792e-05 | 0.00287042 | missense | ARMC4 | GRCh38.p7 | 10:27944874 | TCCAGGCCTCCAACA[C/T]CTCTGATGGCCAACT | 55130 |
| rs768895834 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27815197 | GCCCACCATCCACTT[G/T]TATTCTTCATTCATT | 55130 |
| rs768909502 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27951677 | TAGAAATTATTTTTG[C/T]CCATTTAGAATGGCT | 55130 |
| rs768925246 | snp | A/C | 5.14275e-05 | 0.00507061 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940853 | AATCTTAAAAAGAAC[A/C]TTTAAGGCATTCTTC | 55130 |
| rs768933445 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27928402 | GGTTAGTTTAAGCCA[C/T]CTTCACCTCTCACCT | 55130 |
| rs768934760 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27992833 | CAGATGTGATCACGT[C/T]TGTGCTTGGAGCACA | 55130 |
| rs768942297 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27939671 | TCAGCCCAGGAGATT[G/T]AAGTGACAGTGAGCT | 55130 |
| rs768972871 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27855779 | ATTCAGCAGTTCCAA[C/T]TGAACTGCTCTCCAC | 55130 |
| rs768980450 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27933598 | AGAGAGGAGGAAATG[A/C]ATTCAAAGAACATCA | 55130 |
| rs769035182 | snp | C/T | 6.6024e-05 | 0.00574523 | missense | ARMC4 | GRCh38.p7 | 10:27940783 | GGTTTTGTGGAATCA[C/T]GTGCACAGTCTAGTA | 55130 |
| rs769049061 | snp | A/T | 0.000122003 | 0.0078094 | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27958890 | CTGGTCTTTCCAACG[A/T]CAAAGATCATGCTTC | 55130 |
| rs769055222 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27813506 | AGAACATTTAAAATC[A/T]AGCAATTATGATTCT | 55130 |
| rs769070494 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27812938 | TTTTCCACCTCTCAG[A/G]ACAAGCCAACAGCAT | 55130 |
| rs769094408 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27911465 | TATTTTAATGGACCA[C/T]TGGGAAACTACAGTC | 55130 |
| rs769105694 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27863012 | AACTTTTTCTCTTAG[A/G]AGAAACATAGGACTA | 55130 |
| rs769133632 | in-del | -/AAA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27970996 | AATAAATAAATAAAT[-/AAA]TAAATAAATAAACAA | 55130 |
| rs769141195 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27947088 | GTCATGTTCTTACAG[A/C]TTTTAGTATCTTTTC | 55130 |
| rs769141612 | snp | C/T | 1.74686e-05 | 0.00295534 | intron-variant | ARMC4 | GRCh38.p7 | 10:27862407 | TCAGGACAATATGCA[C/T]GTAAAACAAAAAGAT | 55130 |
| rs769150970 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983569 | CTGTGTAATGAATCA[A/G]TGAAGTGATTACGTT | 55130 |
| rs769154441 | in-del | -/ATA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27849546 | CCTAGAACTTAAAAT[-/ATA]ATAATAATAATAATA | 55130 |
| rs769160167 | in-del | -/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27977716 | ACTGAATAGCCCAAT[-/G]AAAAAAACAGACAAA | 55130 |
| rs769187771 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27928643 | TTCAATTTATGGCAA[A/G]TTAAATAACATGTCT | 55130 |
| rs769224754 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27859487 | TACTATTCCTCCTAA[C/G]ATGTTTCATATCTAG | 55130 |
| rs769251005 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27850073 | AATTTATGATGTCAC[A/C]TCATATATTGATGGT | 55130 |
| rs769255131 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27877019 | TCCCTTGGGATATAG[A/G]CTCATGTCTATCACT | 55130 |
| rs769284744 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27921300 | ACCCCACCTCCAACG[-/A]AAAAAAAAAAGAAAA | 55130 |
| rs769299244 | snp | A/C | | | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27981913 | CTACTCTGAAAATGC[A/C]TTATGACCTCACGAG | 55130 |
| rs769301360 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27872874 | TGCTGGCCTCATAAA[A/T]TGAGTTAGAGAGGAT | 55130 |
| rs769338548 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27864236 | TTGAGATGATTCCCA[C/T]GTCTCTGGCTCAACT | 55130 |
| rs769346541 | in-del | -/TC | 0.000165202 | 0.009087 | frameshift-variant, utr-variant-5-prime, intron-variant | ARMC4 | GRCh38.p7 | 10:27981544 | ATAAATTGAACCTTT[-/TC]TCTCATAATTAACGT | 55130 |
| rs769348690 | snp | C/T | 3.17254e-05 | 0.00398267 | missense | ARMC4 | GRCh38.p7 | 10:27985146 | CAAGAATATTTAATG[C/T]AATTGAGTTTTCTTT | 55130 |
| rs769364134 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27891039 | TGTTTATAGCAATAT[G/T]CCTAGCATGAAACTA | 55130 |
| rs769368267 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27923001 | AGGATGAGGACACTG[C/G]AAAAATTTATAGGTA | 55130 |
| rs769370187 | snp | A/G | 1.68496e-05 | 0.0029025 | intron-variant | ARMC4 | GRCh38.p7 | 10:27936913 | CAGAGGCTGTCAGTC[A/G]TCAAGGAATATCAAG | 55130 |
| rs769379926 | snp | G/T | 1.64923e-05 | 0.00287156 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27944379 | AGGTCAACAATATTC[G/T]GTCTGATTTGAGGAT | 55130 |
| rs769381334 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27845566 | GATCAAATTCACACA[C/T]AGCAATATTAACTTT | 55130 |
| rs769381751 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27817063 | CCTGTTATGCAGTTT[G/T]ATACATACACACAGA | 55130 |
| rs769397851 | in-del | -/A/AA/AAA | 0.535734 | 0.123907 | intron-variant | ARMC4 | GRCh38.p7 | 10:27985216 | TCTCTGTTAGCTGCC[-/A/AA/AAA]AAAAAAAAAAAAAAG | 55130 |
| rs769417157 | in-del | -/AGT | 3.78136e-05 | 0.00434803 | intron-variant | ARMC4 | GRCh38.p7 | 10:27987592 | TGCTACCTAGAGGTC[-/AGT]AGAAGTTAAATTTAA | 55130 |
| rs769418256 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27956465 | AGCATTTCAGAGTAT[A/G]GGCAGATATCCAACT | 55130 |
| rs769457495 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27996752 | AGCATTTTGGAAAAT[A/G]ACACCATTGATGGCA | 55130 |
| rs769475522 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27973050 | ACTAAAATCATATAA[A/G]CATCTTAATACATTG | 55130 |
| rs769530979 | snp | C/T | 3.29669e-05 | 0.00405984 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27812567 | CGGATATTGGATATA[C/T]AACCAGCTGCAGCTT | 55130 |
| rs769535957 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27865630 | CAGGAGGGTGAGGAC[-/T]CTTGCTGTCTCATTC | 55130 |
| rs769544116 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27870983 | CCAACAGTGTGAAAG[C/T]GTTCCTATTTCTCTA | 55130 |
| rs769547371 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27916077 | AGTGGTGCAACCCAA[C/T]GCGGGAAGTCAGAAC | 55130 |
| rs769554961 | snp | A/C | 3.30923e-05 | 0.00406756 | missense, intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27971272 | GGGGGCTTTGCCAAG[A/C]TGATCCTTTTCCTTT | 55130 |
| rs769581668 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27965091 | GGTTTTCCTCTTGGG[C/G]TTTCAGGTTTTTCAA | 55130 |
| rs769582792 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27843503 | GGGCATGGTGGCTCA[C/T]GCCTGTAATTCCAGC | 55130 |
| rs769601424 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27932080 | GCTAGGACTACAGGC[A/G]CACACCCTCACATCC | 55130 |
| rs769606517 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27868664 | GGGAAGGGAATAACA[C/T]ACATTGGGGCCTGCT | 55130 |
| rs769611765 | snp | C/G | 1.70237e-05 | 0.00291746 | intron-variant | ARMC4 | GRCh38.p7 | 10:27994913 | AGAAGCAAGTAACTG[C/G]CTTACCTGACAACAT | 55130 |
| rs769613080 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27956880 | ACCCATTTGCATGAA[A/T]TTATAACATATAGTA | 55130 |
| rs769683129 | snp | A/T | 1.64993e-05 | 0.00287218 | utr-variant-3-prime, intron-variant | ARMC4 | GRCh38.p7 | 10:27812498 | TTTGATAGCTTGTAA[A/T]GTCCATTTAAATTTC | 55130 |
| rs769686728 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27986462 | TGAATAATCCTTCAT[C/G]TATTAACTACCTCCT | 55130 |
| rs769690437 | snp | A/G | 1.69746e-05 | 0.00291325 | missense | ARMC4 | GRCh38.p7 | 10:27987526 | TTATCAACTTCTTCT[A/G]ATTTGACTGTTGTTT | 55130 |
| rs769708918 | snp | C/T | 8.25512e-05 | 0.00642408 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27907747 | CAGCAGGGACCACAA[C/T]AAACGAACTCCATCT | 55130 |
| rs769714252 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27880595 | AGTCATGAGGATGGA[A/G]CTCTAGTGAGTGGAA | 55130 |
| rs769732564 | in-del | -/ATTG | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27836785 | TAATAATTACTATCA[-/ATTG]ATTGATTAATAATGT | 55130 |
| rs769745511 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27854456 | CCGGAAATAAATATT[C/T]ATTAACAAATGAAAG | 55130 |
| rs769781324 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27918176 | TCAACTTGTCCTATA[C/G]GGCCTGCATAAACCT | 55130 |
| rs769786133 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27964153 | CTTGAACCTGGAAGG[C/T]AGAGGTTGCAATGAG | 55130 |
| rs769812824 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27867556 | AATGCACCCTGCATC[A/C]CTGTGAAGATGACAA | 55130 |
| rs769814452 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27950461 | GAGAATACTGTTTCC[C/T]GAAGAAAAATATACA | 55130 |
| rs769819591 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27977931 | ACATTGCCTACATCA[A/G]TGTAAAATATTGCAA | 55130 |
| rs769820053 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27895686 | TGTGGCTAGTAGTTG[C/T]CGTATCTGAACAATA | 55130 |
| rs769838786 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27816676 | GATTTTACAGATGAA[C/G]TTCCTTTGAGTATTG | 55130 |
| rs769841821 | snp | A/G | 1.64879e-05 | 0.00287118 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27860643 | TACTGCACCATTCTC[A/G]TGCATGGTGATGCAG | 55130 |
| rs769869237 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27906353 | AATCACTAAAAAGTC[A/T]GGAAACAACAGATGC | 55130 |
| rs769871141 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27894429 | AATAAACTATTATTT[C/T]ATGTACCACCAAGAA | 55130 |
| rs769894665 | snp | A/G | 1.65048e-05 | 0.00287265 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944993 | GCCAGAGAAAGGTTA[A/G]GGAACACCGCATTCC | 55130 |
| rs769925622 | snp | C/T | | | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27959058 | AGACTATGTCTTGGA[C/T]GGGCTTAGAGGCTCA | 55130 |
| rs769950300 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27952394 | AACTTTTTTTATTTT[-/A]TTTTTTTTTTTTACC | 55130 |
| rs769995150 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27813067 | GGGACTCTCAGTGCC[A/T]ACTAACTAGAGCTGA | 55130 |
| rs770011677 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27840025 | ATTAATAATTTACAT[C/G]GATTTAACTCACAAA | 55130 |
| rs770025038 | snp | A/G | 1.65861e-05 | 0.00287972 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940546 | GAAGGCAAGGGAAGC[A/G]GAACTGGCATGAGTA | 55130 |
| rs770032805 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27901521 | GACATAGATTGGCAA[A/C]TTGGATAAAGATCAA | 55130 |
| rs770056330 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27979711 | CATTGCTGAAAGCCA[G/T]TAAATATACAAATAA | 55130 |
| rs770059788 | snp | A/C/T | 9.90318e-05 | 0.00703613 | missense, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983931 | TAACAAATTTCCCCA[A/C/T]GAATTTGTCTCCACG | 55130 |
| rs770081308 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27929508 | TTAATATTTAAATGA[A/G]TTCAAAGGTTTCCAC | 55130 |
| rs770085054 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27912998 | GTCTTGGGATAAGTA[C/T]GTCAGAAATTCTTTA | 55130 |
| rs770095069 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27881674 | GCCGGCAAAAATACA[C/T]CCTTGACTATTATTA | 55130 |
| rs770097987 | snp | C/G | 1.67253e-05 | 0.00289178 | utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27995158 | GGGATCCACCGTGCT[C/G]AGACCTGAGCTTAGC | 55130 |
| rs770099876 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27837730 | TTGCTCATGGGTAAA[A/C]AAAGACGTAGAGAAT | 55130 |
| rs770118021 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27903899 | CACCAACCAGGGAGA[C/T]CACTGTCCCAACCAG | 55130 |
| rs770119302 | snp | C/T | 1.65693e-05 | 0.00287826 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984028 | CCTTAACCTAGAGTT[C/T]GGTAAAAAGTGTTGG | 55130 |
| rs770119903 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27878010 | TTTCACTATACACTG[G/T]GCACTTAAGACTTGA | 55130 |
| rs770196114 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27947303 | GATATTTTATAAGCC[A/G]TAAAGAAGAATCTAG | 55130 |
| rs770219489 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27924664 | AGCCCACATTATACA[A/C]AAATTTAAAATGACA | 55130 |
| rs770242768 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27850217 | TGGGAGGCCAAGACG[A/G]GTGAATCACTTGAGG | 55130 |
| rs770250660 | snp | A/G | 0.000116761 | 0.00763982 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944216 | GACAACATCACGGCT[A/G]CTCACCAGTTTGGTG | 55130 |
| rs770294804 | snp | C/T | 0.000169408 | 0.00920193 | missense | ARMC4 | GRCh38.p7 | 10:27985161 | CAATTGAGTTTTCTT[C/T]CATTGTATTATAATC | 55130 |
| rs770296963 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27840843 | GTTTGAGTTATGAAG[A/T]AATTTATTGATTTAT | 55130 |
| rs770297812 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27926401 | TGATGGCAGAGGCGG[-/A]AAAAAAAAAAAACTT | 55130 |
| rs770301470 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27828745 | GGTTTATAACTTTAC[C/T]CTAGGAAATGCTAAG | 55130 |
| rs770307316 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27864824 | TTTTGCATCCCAACG[C/G]CGTATCAGGCATGGT | 55130 |
| rs770329274 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27911124 | TTAGGAACACTGGGC[A/G]GCACTTCAGCACTAT | 55130 |
| rs770330978 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27979074 | AATTCGCAGAGCATG[G/T]TGGCAGATGCCTGTG | 55130 |
| rs770345382 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27862220 | AGCTTCTATTTTACA[A/C]GGATCTTGTAATACT | 55130 |
| rs770383472 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27971621 | TGACTAAAACACATC[A/G]TATTTAAATGGCTTG | 55130 |
| rs770389143 | in-del | -/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27845792 | CTCTGATAAAACAGA[-/C]TTTTAAACCAACAAA | 55130 |
| rs770427078 | snp | G/T | 1.72731e-05 | 0.00293875 | intron-variant | ARMC4 | GRCh38.p7 | 10:27862420 | CATGTAAAACAAAAA[G/T]ATGTGTTACTTACTG | 55130 |
| rs770427120 | snp | G/T | 1.65018e-05 | 0.00287239 | missense | ARMC4 | GRCh38.p7 | 10:27939956 | CACTATTTAGGTTCT[G/T]GACAAGGTTTTCAAT | 55130 |
| rs770436833 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27987009 | TTGGCAGTATGCCGA[A/G]AGAGAGTGGATTCAG | 55130 |
| rs770479946 | snp | G/T | 3.30028e-05 | 0.00406205 | synonymous-codon, intron-variant | ARMC4 | GRCh38.p7 | 10:27971125 | TTTGTAATTAACAGT[G/T]GTCTTCCAGTTTAAG | 55130 |
| rs770507019 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27858823 | TTTTTTTTTTTTTTG[-/A]GACAGAGTCTCGCTC | 55130 |
| rs770509619 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27909461 | CACCCCAAACCTTAG[G/T]CAATTCATCAGCTAC | 55130 |
| rs770514657 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27870276 | CTTCTCTTTGGCATA[A/G]TCTACACTCCAGCCT | 55130 |
| rs770527140 | snp | A/T | | | missense, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983887 | AAGTAATGCACAGAG[A/T]CTCACCATCGTGAGG | 55130 |
| rs770539111 | in-del | -/G | 1.65179e-05 | 0.00287379 | frameshift-variant, intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27971256 | TGCTTCTTCCTTCTT[-/G]GGGGGCTTTGCCAAG | 55130 |
| rs770545877 | in-del | -/AG | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27924030 | AAGAAAGAAGGAAAG[-/AG]AGAAAGAAAGAAGGA | 55130 |
| rs770551894 | in-del | -/CGAGATTGCACCA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27835874 | GGGGTGGCAGTGAGC[-/CGAGATTGCACCA]CTGCACTCCAGCCTG | 55130 |
| rs770558529 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27899386 | CACAAAACTGGGGGG[C/T]CATTTCAGCAGACAC | 55130 |
| rs770602131 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27957566 | CTTCCTTTAGAATTA[A/G]GGTACAGCATCATCA | 55130 |
| rs770607602 | snp | A/C/G | 3.29991e-05 | 0.00406185 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27944398 | TGATTTGAGGATTAT[A/C/G]ACTGATTTCCTTCAG | 55130 |
| rs770628809 | in-del | -/CTT | 1.64795e-05 | 0.00287045 | cds-indel | ARMC4 | GRCh38.p7 | 10:27940657 | GAGGAATGCCCCCAG[-/CTT]CTTTGCGGATGGCTT | 55130 |
| rs770652602 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27918479 | TAGATAAAAAGCATC[A/G]TATAAAATTCAAAAA | 55130 |
| rs770673788 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27868306 | CCAGAAATAAAATTT[G/T]ACCTAGAAATCCCAT | 55130 |
| rs770684381 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27904023 | CCTGTTGCCAAAAAG[C/G]GTATATGCAGACAAC | 55130 |
| rs770685107 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27816939 | ATTTTTAGTAGAGAC[A/G]GGGTTTTGCCATGTT | 55130 |
| rs770711530 | snp | A/C | 1.65759e-05 | 0.00287883 | intron-variant | ARMC4 | GRCh38.p7 | 10:27934964 | GACCTCCCAAGTGTT[A/C]TCCCTAACACTTATA | 55130 |
| rs770730346 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27952817 | TTGGTATGTTACTGG[G/T]AGAGTGTAAATTGAT | 55130 |
| rs770742605 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27857297 | TCTTCCTCTAGCTAA[G/T]TTTATTGTACTAATA | 55130 |
| rs770774299 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27885207 | AACAAAATGAGAATA[C/T]AAACAAGGAGACAGA | 55130 |
| rs770781726 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27933302 | TCCAGACAATTGATA[C/T]TTGCAAGTAAAAGAT | 55130 |
| rs770787892 | snp | C/T | 6.93313e-05 | 0.00588735 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944472 | GGCGAATATGTAACC[C/T]GTGCTATGTTTTTAA | 55130 |
| rs770815840 | in-del | -/CGGGGACTGCAGGGC | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27938875 | AAAGTGCTGGGAATA[-/CGGGGACTGCAGGGC]CGGGTACAGCCCCTT | 55130 |
| rs770840870 | in-del | -/AC | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27900666 | AACTTCGTGAAGCAT[-/AC]ACACAAGTACCAATA | 55130 |
| rs770897275 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27964551 | AGAATGCTGTCTTTC[A/G]GTATCTTTGTTAAAC | 55130 |
| rs770914477 | in-del | -/CTGT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27850712 | ACTGGATTTACCTTC[-/CTGT]CTAAAATAATTTAAA | 55130 |
| rs770915773 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27904857 | GGGCATCTTGATGAT[A/G]AGCTGTGATAGCCAA | 55130 |
| rs770926116 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27897166 | CATCCCCTTCCCACC[C/G]GCCTGCCTTCTTTCT | 55130 |
| rs770927145 | snp | A/G | 1.64868e-05 | 0.00287109 | synonymous-codon, missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27812518 | ATTTAAATTTCAAGT[A/G]TATCTTGCCTTCTCT | 55130 |
| rs770934383 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27929727 | GGCAATATTTTTTCT[A/C]TCTCAGGATGTTTTA | 55130 |
| rs770934456 | snp | A/G | 1.64893e-05 | 0.0028713 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27940754 | CTCTGGCCTCATACA[A/G]ACTCGATTGGGCAGG | 55130 |
| rs770935247 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27817714 | GGCATATATGTACCA[C/T]ATTTTAAAAATCCAA | 55130 |
| rs770937518 | in-del | -/AAG | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27976314 | TAGGAAGGAAGAAAT[-/AAG]AAAATGATCTTTACT | 55130 |
| rs770956645 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27864526 | GAGTGAGGTGAGAGC[A/G]GGGAGTGAGGTGAGA | 55130 |
| rs770957763 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27992969 | CACCCAGGCTGGAGT[C/T]CTGTGGTGCAATCTC | 55130 |
| rs770958408 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27883338 | AAAATGCATATTTTA[C/T]AGAATTAGCCCAAGA | 55130 |
| rs770959498 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27856083 | GCTACAGTTTTGTTA[A/T]AATTAGCAAATAACT | 55130 |
| rs770965382 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27827031 | ATGCATCCAGGGGAC[A/G]CTTTTGGTTCTTGTC | 55130 |
| rs771000580 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27876091 | GCTCAAGGATGCCTG[C/T]CTGTCACTGTAGACT | 55130 |
| rs771003553 | in-del | -/AAAAAAAAAAAA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27943811 | CAAAAAAAAAAAAAA[-/AAAAAAAAAAAA]AAAAAAAAGGCATCA | 55130 |
| rs771009714 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27881923 | CACCTGTAATCCTTT[C/T]GGGAGGTTGAAGTGG | 55130 |
| rs771014848 | snp | C/T | 1.64798e-05 | 0.00287047 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27940653 | CAACAGAGGAATGCC[C/T]CCAGCTTTGCGGATG | 55130 |
| rs771055913 | snp | A/G | 8.24314e-05 | 0.00641942 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27995080 | TAGAGGGGTGATTTC[A/G]AGGATTCCAGTTCCA | 55130 |
| rs771083423 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27990472 | TGGGCCACTGCACCC[A/G]GCCCCATTTAGTGTC | 55130 |
| rs771089875 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27814102 | TGAAAAATTAGGCTC[A/G]CAGACAATTTGAAGG | 55130 |
| rs771128953 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27815054 | GAAGATGACCAATAA[A/G]GTCTCCTTCATAAAC | 55130 |
| rs771141514 | snp | C/G | 1.64825e-05 | 0.00287071 | missense | ARMC4 | GRCh38.p7 | 10:27860785 | AAGGCCACTCTATTC[C/G]TGCCCCACATACAGC | 55130 |
| rs771144051 | snp | C/T | 1.66106e-05 | 0.00288184 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27994933 | CCTGACAACATAACC[C/T]GATTCAAATGCTGAG | 55130 |
| rs771154993 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27864011 | TGAAGTGTGGGGGAA[A/G]GATTTTTATCAATTT | 55130 |
| rs771155775 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27852025 | TAAAATGGAGCACCA[C/T]GTTTAAAGTTGGGAA | 55130 |
| rs771176376 | in-del | -/TTAA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27836759 | ATTAGTGGTTTTGAC[-/TTAA]TTAATTATAATAATT | 55130 |
| rs771191335 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27865556 | TCCTGTATGACAGCA[C/T]CTATCACTGCACATA | 55130 |
| rs771197791 | snp | A/G | 3.35587e-05 | 0.00409613 | synonymous-codon, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27961574 | CTTTCTTACCTTTAA[A/G]TATTTCACCAGCTTC | 55130 |
| rs771233084 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27974744 | TTCTGGTTCCATATG[A/C]ATTTTAAAATAGTTT | 55130 |
| rs771236273 | in-del | -/TTTG | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27861707 | CAGACGATATCCTTC[-/TTTG]TATACGTAATTGCCC | 55130 |
| rs771236503 | snp | A/G | 1.65135e-05 | 0.00287341 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984163 | TAAATAACATAAAAT[A/G]AGCCTGAGAAAACAT | 55130 |
| rs771255354 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27988799 | CAGAATAATGTTCAC[A/G]TCTGAATCCCCAAAA | 55130 |
| rs771272872 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27988429 | TGCAACCTCTGCCTC[C/T]GGAGCTCAAGCAATC | 55130 |
| rs771277158 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27937026 | AGTAAAATATAATTC[A/G]TCTTTCTACTAGTAG | 55130 |
| rs771279442 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27923149 | TACGACATTGTTGAA[A/C]CTAAACATTATTCAT | 55130 |
| rs771367246 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27925103 | CTACAGACCAATATC[A/T]CTCATGAATATTATT | 55130 |
| rs771380289 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27877366 | AGGTGCATGGTATGA[A/G]ATACCAGGAGCCAAA | 55130 |
| rs771413885 | snp | A/G | 1.68001e-05 | 0.00289823 | intron-variant | ARMC4 | GRCh38.p7 | 10:27935296 | TGGTTTTTGTATAAG[A/G]TTTGCTAAAAATTAC | 55130 |
| rs771454081 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27878395 | AACTGGGTGTTTTGG[C/T]GTAAAGCAATTAAAT | 55130 |
| rs771457896 | snp | C/G | 1.64923e-05 | 0.00287156 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27971145 | TCCAGTTTAAGCTTG[C/G]TTCCCATCTCTTGGT | 55130 |
| rs771487703 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27885217 | GAATATAAACAAGGA[A/G]ACAGAAAAAATAGGC | 55130 |
| rs771512100 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27956667 | TCTCGGCATTATTCT[A/T]GTCTTCTCAATGTTT | 55130 |
| rs771550996 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27821867 | CTTTCAAACTTTTCT[A/C]TTTTTAATCCTCCGC | 55130 |
| rs771553322 | snp | A/G | 1.85951e-05 | 0.00304913 | intron-variant | ARMC4 | GRCh38.p7 | 10:27907625 | TTCAGTATAGTATTA[A/G]AGATTCTAGAAGAGA | 55130 |
| rs771553632 | snp | A/G | | | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:28000330 | CCTAAAGGAGATACT[A/G]CCTGCAGAGAAGCTT | 55130 |
| rs771560616 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27887995 | TGAATCATGAAGAAA[A/C]AGAAAATCTGAACAG | 55130 |
| rs771566473 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27844627 | TCAATTTCTTTATCT[A/G]TAAAACTAAGATAAT | 55130 |
| rs771573181 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27819129 | TTTCCCCTTCCTATT[C/T]TGTCTGATGATTCCC | 55130 |
| rs771573217 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27820864 | CTCAGCTCACTGCAA[C/T]CTCTGACTCCCGGAT | 55130 |
| rs771598537 | in-del | -/AGAG | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27924047 | GAAAGAAAGAAGGAA[-/AGAG]AAAGAAAGAAAGAAA | 55130 |
| rs771610894 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27826154 | GACGCAGAATGGGAT[A/C]AAGAACATCAAGAGG | 55130 |
| rs771620286 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27881048 | CTTTCAGCAAACTAC[-/T]TTAACTTCTCTAAGC | 55130 |
| rs771639674 | snp | A/C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27985310 | CAAAGTCCATTCAGA[A/C/T]GTGTTTCTTTCATTA | 55130 |
| rs771640361 | snp | A/C | 3.30202e-05 | 0.00406313 | stop-gained, intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27971247 | GGAGGGCAGCTGCTT[A/C]TTCCTTCTTGGGGGC | 55130 |
| rs771643379 | snp | A/G | 1.66161e-05 | 0.00288232 | missense | ARMC4 | GRCh38.p7 | 10:27862594 | AGTTCCAAACCACCA[A/G]CAAAGGAACGAACCA | 55130 |
| rs771651575 | in-del | -/TT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27921832 | GGCAATAGAGCAGTA[-/TT]TTATTTTTTTTTTTG | 55130 |
| rs771660573 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27945211 | AGGTGGTATTCATCT[A/G]TTAAAGAGTCATGGG | 55130 |
| rs771662244 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27889054 | ATTTAGTTTAGATTT[C/T]ACAGGACAATAAAAC | 55130 |
| rs771681283 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984114 | CTTGTAATGTAGACA[C/T]TGAAAGCATTTTGCA | 55130 |
| rs771701933 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27933396 | AGTATTAAAATGGAT[C/T]TTAGCATTGAGAAGT | 55130 |
| rs771703533 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27976439 | TCAGCATACAAAAAT[C/T]AAGTGTATATTTATA | 55130 |
| rs771704817 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27832913 | GAAAAGAATAAGTAA[C/T]AGGAATAATTTTTTT | 55130 |
| rs771713007 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27852653 | TAGAAAACAAATAAC[-/A]AGATGGTACATTTAA | 55130 |
| rs771734880 | snp | A/C/G | 4.13285e-05 | 0.00454564 | missense, synonymous-codon, intron-variant | ARMC4 | GRCh38.p7 | 10:27944224 | CACGGCTACTCACCA[A/C/G]TTTGGTGATACCCCC | 55130 |
| rs771774254 | in-del | -/AT | | | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999342 | TTTTTACATTTTTCC[-/AT]ATAGGCTTCCAGACA | 55130 |
| rs771789712 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27920020 | AGAAACAAAACTAAG[C/T]TATAGTTTATAGGGA | 55130 |
| rs771797281 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27904966 | CTTTAACATAAATAT[C/T]GTTTGTGTTTATCAA | 55130 |
| rs771800841 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27850528 | TACTACTACACTCTA[G/T]ACTGGGTGACAGAGC | 55130 |
| rs771837765 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27941730 | CTCCCTAGAGCTGCA[A/T]TTGGCTGTCAGCCTT | 55130 |
| rs771873183 | snp | C/T | 1.64787e-05 | 0.00287038 | missense | ARMC4 | GRCh38.p7 | 10:27944859 | AAATTTATCAGCACT[C/T]CCAGGCCTCCAACAT | 55130 |
| rs771890705 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27953059 | TTTGATGAGTTTGGG[C/T]ATATGCATATAAATC | 55130 |
| rs771902781 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27818752 | CAGTCCTTGGCCTCC[C/G]CGCTCATAGTTCTGG | 55130 |
| rs771914028 | snp | C/T | 1.68525e-05 | 0.00290275 | missense | ARMC4 | GRCh38.p7 | 10:27985195 | GCCCAGGATTTTTAC[C/T]ATGGGGTCTCTGTTA | 55130 |
| rs771920114 | snp | A/C | 1.65091e-05 | 0.00287303 | stop-gained | ARMC4 | GRCh38.p7 | 10:27939980 | TTTCAATGATCCTTT[A/C]TGCTTTGATTGCAGC | 55130 |
| rs771932492 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27962275 | ACAGGTATTTGAACT[C/T]ATTTATTTAACTAAA | 55130 |
| rs771955374 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27857498 | GGTTAAATATATTAC[C/T]AAAATTAATTTCACT | 55130 |
| rs771958359 | snp | A/C | 1.65803e-05 | 0.00287922 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944765 | GAGCTAAGAAGAGAG[A/C]CCAGGAAGGTGGGAA | 55130 |
| rs771984634 | snp | C/T | | | missense, intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27971262 | CTTCCTTCTTGGGGG[C/T]TTTGCCAAGCTGATC | 55130 |
| rs772019960 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27902608 | CAATAAAAAATGATA[C/G]AGGGGAGATCACCAC | 55130 |
| rs772028860 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27921459 | ATCATGTATGCCAGG[G/T]AGTTTGTATAAAAGA | 55130 |
| rs772042716 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27825788 | CAAATTAGACTTTGC[C/T]TAGGGCATGGAAAGC | 55130 |
| rs772056135 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27993372 | ATAAGATTTCAGGCC[A/G]GGCGTGGTGGTTCAC | 55130 |
| rs772070248 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27867379 | TAGGCCTGAGTTCCA[C/T]GAATTGGTAAAACTA | 55130 |
| rs772108733 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27979881 | AAAATTCATAAACAG[C/T]GTCAAGGAATACCGA | 55130 |
| rs772112361 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27895781 | GTGTAAATAATGAGA[C/T]GCTATTATTAAACAG | 55130 |
| rs772128860 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27852631 | GAGAAAAAGCAGATG[A/G]GAAAAATAGAAAACA | 55130 |
| rs772137537 | in-del | -/T | 3.67404e-05 | 0.00428589 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940055 | AGACGTGAATATAAG[-/T]TAACTGTTTACATTT | 55130 |
| rs772137722 | snp | A/G | 1.70078e-05 | 0.0029161 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940847 | CATGGAAATCTTAAA[A/G]AGAACATTTAAGGCA | 55130 |
| rs772151957 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27839006 | TTTTGATATCCAAAC[C/T]TATTTAAATTTGGAG | 55130 |
| rs772159007 | snp | A/C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27908241 | TAATCTAGCATTAGG[A/C/G]ATTAAAATCATTACA | 55130 |
| rs772172116 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27877068 | ATTTGTTGAATTGTG[-/A]AAAAAAAAAGGCAGT | 55130 |
| rs772185029 | snp | A/C | 1.6483e-05 | 0.00287076 | missense | ARMC4 | GRCh38.p7 | 10:27935115 | AGTGGTTGAATGCCA[A/C]CACATTTCCGGACAA | 55130 |
| rs772193752 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27858830 | TTTTTTTGAGACAGA[A/G]TCTCGCTCTATCACC | 55130 |
| rs772227784 | snp | C/T | 1.64914e-05 | 0.00287149 | missense | ARMC4 | GRCh38.p7 | 10:27940762 | TCATACAGACTCGAT[C/T]GGGCAGGTTTTGTGG | 55130 |
| rs772239137 | snp | C/T | 1.64982e-05 | 0.00287208 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27812591 | GCAGCTTCCTGGAGA[C/T]CCTGGTCAGGGGACC | 55130 |
| rs772252306 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27990465 | ACTGGCATGGGCCAC[C/T]GCACCCGGCCCCATT | 55130 |
| rs772264092 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27950369 | ATTGCTTTCCTTCTG[C/T]TTATTTGCAAATCTA | 55130 |
| rs772267642 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27907084 | TCTCTAAACCTATAG[-/A]AAAAAATGTTAAGAG | 55130 |
| rs772273452 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27836841 | ATTGAATAATTATCA[C/G]AGCAAAAACTTGAAA | 55130 |
| rs772280483 | snp | G/T | 1.71519e-05 | 0.00292842 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983805 | AGCTAACAATCAAAG[G/T]CCACTGGCTTTAGTT | 55130 |
| rs772287643 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27884396 | ACCCACACTTGAAAC[A/G]TAAAATTTCCTGGCA | 55130 |
| rs772303854 | snp | A/G | 0.000236985 | 0.0108828 | missense, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27985053 | AATGATTGAGGAGGT[A/G]CAGATCCAATTGCTT | 55130 |
| rs772332965 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27861524 | ATATCCTTAAAGGGA[C/T]ACTGCACTTAACTGG | 55130 |
| rs772337187 | snp | C/T | | | intron-variant, missense | ARMC4 | GRCh38.p7 | 10:27835982 | TACATTTACTATACA[C/T]TAAGTGGAAGTGGAT | 55130 |
| rs772348836 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27938329 | TAGGCCCTGCTCCAA[C/T]AGGACTGCTGTCCAA | 55130 |
| rs772361042 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27818961 | CTCCCAGTCACTGGG[A/C]ACATCACTGAACCTC | 55130 |
| rs772380101 | in-del | -/C | 1.65201e-05 | 0.00287398 | frameshift-variant | ARMC4 | GRCh38.p7 | 10:27995115 | GGCAGCAGTCCACTG[-/C]CGTCAATTTCCTCAG | 55130 |
| rs772442251 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27992350 | AAGGGGTAATTGTTT[A/C]AAAATGTCAAAATGC | 55130 |
| rs772451192 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27816356 | GATTCTGTTCTGTAT[A/G]AGGGAAACAGGGAAG | 55130 |
| rs772460736 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27823194 | CTCAAGTTGCTCTTG[A/G]ATTTTTATTCCTATT | 55130 |
| rs772461494 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27946208 | ATTACATATAATATA[C/T]AAATATAAAAAATAC | 55130 |
| rs772469122 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27957707 | ATATAAAACTTGCAG[A/G]TTGAAATTAACATAT | 55130 |
| rs772486185 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27975668 | TAAAGAATATTCCAG[A/G]CCCAGATGGCTTTCA | 55130 |
| rs772501402 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27861571 | GGATTTCTCCACCCT[A/G]GGAATACATTGATAT | 55130 |
| rs772504393 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27925520 | ACACTACCATGCTCA[A/G]CTAATTTTTAAAGTT | 55130 |
| rs772537229 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27822133 | TAAGGTTCATGCCCT[C/T]GGCATGCAGCTGTGA | 55130 |
| rs772542366 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27942001 | TGGCCCCAGGAAAGA[C/T]GGGGATGGGGTATGG | 55130 |
| rs772552604 | snp | A/G | 1.64917e-05 | 0.00287151 | missense | ARMC4 | GRCh38.p7 | 10:27860807 | ACATACAGCAACGTG[A/G]AATAGCTTCTGCTAG | 55130 |
| rs772563349 | snp | A/G | 3.29598e-05 | 0.00405941 | missense, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27936787 | TGACAGCAGCTAACC[A/G]CTCTTTATTGTCAGT | 55130 |
| rs772574065 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27977104 | AGTGGATCATAGATA[C/T]AGATTGGAAAGGTAA | 55130 |
| rs772577528 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27892607 | TTCTCCAAAATGAAG[A/T]TTTAAACTTAACTGA | 55130 |
| rs772590376 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27958749 | TTGTATTTCATTTAA[C/T]ATTCTTAATAATTCT | 55130 |
| rs772611516 | snp | A/G | 1.74336e-05 | 0.00295237 | intron-variant | ARMC4 | GRCh38.p7 | 10:27862410 | GGACAATATGCATGT[A/G]AAACAAAAAGATGTG | 55130 |
| rs772612777 | snp | A/G | | | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999256 | TCGTGAGCAGTTGCG[A/G]GGTCGGCGGCAAGTT | 55130 |
| rs772614819 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27815627 | TCTTCTACCGTACTC[C/G]CCTGCTTTTCCTCGT | 55130 |
| rs772621472 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27911349 | ACGTGTCCAGGAATG[A/G]CAGCGCAAGTGATGT | 55130 |
| rs772624926 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27862816 | TGTACATATGTATAA[A/G]TCTATATACATATGT | 55130 |
| rs772635867 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27904346 | TGGCAGGAAGCAGAG[C/T]GGGAATCTTGGGCTG | 55130 |
| rs772636599 | snp | C/T | 1.64827e-05 | 0.00287073 | missense | ARMC4 | GRCh38.p7 | 10:27860737 | TTTGATTTCAGATAA[C/T]GCACTAGTGGAGCCA | 55130 |
| rs772648868 | in-del | -/TCTC | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27865848 | AGGGCGAAGCCACTT[-/TCTC]TCTGTAACACGTTGC | 55130 |
| rs772668140 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27996756 | TTTTGGAAAATGACA[C/T]CATTGATGGCAATGT | 55130 |
| rs772704772 | snp | A/T | 3.32127e-05 | 0.00407495 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984317 | GTTTAAAATGTCAGC[A/T]TAAATACTTTAAACA | 55130 |
| rs772721222 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27859509 | CATATCTAGCATATC[C/T]AGATTTGACTAGATA | 55130 |
| rs772722812 | snp | A/G | 1.6656e-05 | 0.00288578 | missense, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27961620 | TCTGATGGCAAATCT[A/G]CACTTGCTTCCTGAC | 55130 |
| rs772725937 | snp | A/G | 1.64773e-05 | 0.00287026 | missense, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27936729 | GCCTTCTCTTACTTG[A/G]TAACATTCTCTTTGC | 55130 |
| rs772739389 | snp | C/T | 1.65203e-05 | 0.002874 | missense | ARMC4 | GRCh38.p7 | 10:27860827 | GCTTCTGCTAGATGA[C/T]GTCTCAATTTATTGT | 55130 |
| rs772753004 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27880388 | AAAAAATTCCTTTGG[A/G]AGGCAGAAAATGTAG | 55130 |
| rs772763679 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27837982 | CACGGCGATGGATTG[C/G]GAAACACAGAGAACA | 55130 |
| rs772771474 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27938598 | TGTATCTGTCTCTTC[-/T]TTTTTCTTTTTTTTT | 55130 |
| rs772789970 | in-del | -/A | 1.64792e-05 | 0.00287042 | frameshift-variant | ARMC4 | GRCh38.p7 | 10:27940647 | CCGAGCCAACAGAGG[-/A]ATGCCCCCAGCTTTG | 55130 |
| rs772793266 | in-del | -/TATATATA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27827382 | CACACACACACACTA[-/TATATATA]TATATATATATATAT | 55130 |
| rs772823968 | snp | C/T | 1.77137e-05 | 0.00297599 | intron-variant | ARMC4 | GRCh38.p7 | 10:27981436 | AGTAACATAATGCTA[C/T]GAAAGCTCAAAAGAA | 55130 |
| rs772846348 | snp | A/G | 1.6492e-05 | 0.00287154 | stop-gained, intron-variant | ARMC4 | GRCh38.p7 | 10:27944380 | GGTCAACAATATTCT[A/G]TCTGATTTGAGGATT | 55130 |
| rs772879659 | in-del | -/AGTAAGCCC | 0.00405103 | 0.044823 | intron-variant | ARMC4 | GRCh38.p7 | 10:27853395 | AAATAAATAAATAAA[-/AGTAAGCCC]TAACTATATGCTGCC | 55130 |
| rs772900783 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27931066 | TGGGTCTCTGATGGC[A/G]AAGTCTTCACTTCTT | 55130 |
| rs772901115 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997751 | AAATGGTGTTCAAAA[A/G]TGGTCGGCATAACTC | 55130 |
| rs772901123 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27981925 | TGCATTATGACCTCA[C/T]GAGCCTTAGTTGATG | 55130 |
| rs772901515 | snp | C/T | 3.29663e-05 | 0.00405981 | synonymous-codon, utr-variant-3-prime | ARMC4 | GRCh38.p7 | 10:27936812 | GTCAGTGTTATTGAG[C/T]AGACTGGCCAAGGGC | 55130 |
| rs772927846 | in-del | -/TG | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27884965 | CTGGTCTGCAAAAAC[-/TG]AGAGAAGTGGCTGTT | 55130 |
| rs772960205 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27898752 | TGATATGTATTGATA[G/T]TGACGAATACATTGC | 55130 |
| rs772962219 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27883843 | GAGACACTCAGTGAG[C/G]ATGATAGATGGGTCA | 55130 |
| rs773013480 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27897586 | TTCATCTGAACTACT[C/G]TAATAGCCCAATTTG | 55130 |
| rs773018767 | in-del | -/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27850544 | ACTGGGTGACAGAGC[-/G]AGACTCTGTCCCAAT | 55130 |
| rs773021114 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27923951 | CTGTCTAATGAAAGA[-/A]AAGAAAGAAAGAAAG | 55130 |
| rs773046497 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27950469 | TGTTTCCCGAAGAAA[A/G]ATATACATATATCCT | 55130 |
| rs773087870 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27828956 | TGCCTTTATATGTAT[A/C]TGTCTTCCAAAATGG | 55130 |
| rs773103656 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27979783 | TGGTTAAGATGGCAA[C/T]ACTATGTAAAGCAAT | 55130 |
| rs773104115 | in-del | -/AAATAAATAAATAAACAAAC | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27970996 | AATAAATAAATAAAT[-/AAATAAATAAATAAACAAAC]AAACAAAATAAAATA | 55130 |
| rs773133050 | snp | A/T | | | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27936531 | CTGAGGCACAGAAAA[A/T]GTCATTGCCAGGTGG | 55130 |
| rs773137657 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27918399 | GAGTCACTTTATTAA[C/T]AGAACAAAAGAAAAA | 55130 |
| rs773173704 | snp | C/G | 1.76278e-05 | 0.00296877 | missense | ARMC4 | GRCh38.p7 | 10:27987533 | CTTCTTCTGATTTGA[C/G]TGTTGTTTCACTAAA | 55130 |
| rs773180298 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27848325 | AAGCAATGGGGGAAG[A/G]ATTCCCTATTTAATA | 55130 |
| rs773183295 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27899085 | ACAGAAAGTGGGTGA[C/T]TTCTGCATTTCCAAT | 55130 |
| rs773187282 | in-del | -/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27834625 | ATGGAGAGGCAGGCA[-/G]GGGGGCAGATCGTGA | 55130 |
| rs773189950 | snp | A/C | 1.648e-05 | 0.0028705 | missense | ARMC4 | GRCh38.p7 | 10:27940637 | TCTTCAGCAGCCGAG[A/C]CAACAGAGGAATGCC | 55130 |
| rs773224852 | snp | A/T | 6.61934e-05 | 0.00575259 | missense, intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27971273 | GGGGCTTTGCCAAGC[A/T]GATCCTTTTCCTTTT | 55130 |
| rs773226329 | snp | A/T | 1.65042e-05 | 0.0028726 | missense | ARMC4 | GRCh38.p7 | 10:27987415 | TGGGCTTCCTTCAAC[A/T]TCCCAGTTTTGGCAA | 55130 |
| rs773256681 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27937665 | TCCAAGCACACAGAT[A/G]TTTTCTGATGCCATG | 55130 |
| rs773276594 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27881708 | AATAATTCTATGTTT[A/G]TATAACTAAAACCAC | 55130 |
| rs773278930 | snp | C/G | | | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27959075 | GGCTTAGAGGCTCAT[C/G]CCTGTAATCCCAGCA | 55130 |
| rs773289116 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27825725 | TCCATAGCCTGGATA[A/G]GGTTATCAGAAGCTG | 55130 |
| rs773324248 | snp | C/T | 1.65121e-05 | 0.00287329 | missense | ARMC4 | GRCh38.p7 | 10:27907751 | AGGGACCACAACAAA[C/T]GAACTCCATCTAAGC | 55130 |
| rs773348552 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27990296 | GGGACTACAGCCGCA[C/T]GCCACCACACCTGGC | 55130 |
| rs773372607 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27838802 | CAAAACTCTCTTTTT[C/T]AGAAGGCAATTATTT | 55130 |
| rs773387106 | in-del | -/ACTG | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27829787 | ATTTCAGTGAAAGAA[-/ACTG]AATGAGTTTTAGAAC | 55130 |
| rs773390746 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27880605 | ATGGAGCTCTAGTGA[A/G]TGGAATTAATGCCTT | 55130 |
| rs773391257 | snp | C/T | 1.65351e-05 | 0.00287528 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984148 | GTAATTATGAAAATG[C/T]AAATAACATAAAATG | 55130 |
| rs773403756 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27813973 | TTATCCAAATAGAAG[A/G]AAATAAAAATGGTAA | 55130 |
| rs773408899 | snp | A/T | 0.00148258 | 0.0271862 | intron-variant | ARMC4 | GRCh38.p7 | 10:27853410 | AGTAAGCCCTAACTA[A/T]ATGCTGCCTACTATT | 55130 |
| rs773448807 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27945580 | AGTCTTGCAAACCAA[C/T]GTCTTCTTGGTGAAT | 55130 |
| rs773452157 | snp | A/T | 0.000708361 | 0.0188063 | missense | ARMC4 | GRCh38.p7 | 10:27944889 | TCTCTGATGGCCAAC[A/T]GGCAGGTTTCTTGAG | 55130 |
| rs773453599 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27986005 | TATGCATTGAGATGG[G/T]GGTGGAGAGGAAGGC | 55130 |
| rs773493458 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27813160 | CTTTCTCCTCTTCTC[C/T]AAGATCATAACTTTC | 55130 |
| rs773501522 | in-del | -/ACAG | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27979470 | CACACACACACACAC[-/ACAG]AGTTAAATGAATTCA | 55130 |
| rs773516719 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27848273 | AATAATACTACACAT[A/C]TACAACCATCTGATC | 55130 |
| rs773523307 | in-del | -/AGAA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27994731 | AAAAATTTAAAACTT[-/AGAA]AGATACTGTGTTGGC | 55130 |
| rs773533635 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27966496 | TTCCAATTGATGAAT[C/T]CTTTGATAGCTAACT | 55130 |
| rs773573331 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27884436 | GCACTTTCTCCACCC[C/G]TTCTCTGGCACAGCA | 55130 |
| rs773596927 | snp | A/G | | | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:28000643 | TCTTCCAAGTTCAGG[A/G]CATTTCACCTTGGTT | 55130 |
| rs773613573 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27889811 | CCAATTTGAGATTGG[G/T]GATCTCATGTTGATA | 55130 |
| rs773626331 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27934774 | TTTCCACATGGGAAA[C/T]TGATTACCGTGTATT | 55130 |
| rs773634929 | in-del | -/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27822930 | ACTTTCCACTAGAGA[-/G]CTTTAATGCCCAAAC | 55130 |
| rs773687588 | in-del | -/AC | 1.67719e-05 | 0.0028958 | splice-donor-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983841 | TTTAAAAATTTACTT[-/AC]ACCATTTAAAAATAC | 55130 |
| rs773689799 | snp | A/C | 1.65124e-05 | 0.00287331 | missense | ARMC4 | GRCh38.p7 | 10:27995110 | ATGTCCGGCAGCAGT[A/C]CACTGCGTCAATTTC | 55130 |
| rs773696573 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27833089 | AAGTTTTTCATATAC[A/C]ACAAAATACATAATG | 55130 |
| rs773727708 | in-del | -/TAAT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27921772 | TTTACAAAGGCAAAA[-/TAAT]TAGACAAGCATCAGA | 55130 |
| rs773738744 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27936106 | GTTAAATGGTCGGGA[C/T]GTGAATCTCTTGTTA | 55130 |
| rs773742953 | snp | A/G | 5.0577e-05 | 0.00502851 | utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27995176 | ACCTGAGCTTAGCAC[A/G]CGCACTACATCAGAG | 55130 |
| rs773749633 | in-del | -/GTC | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27878713 | GAACGGGCAAATCTT[-/GTC]GTCAAAAGTATACTT | 55130 |
| rs773771083 | in-del | -/AAAA/AGAAGGAAAG | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27924012 | GAAAGAAAGAAAGAA[-/AAAA/AGAAGGAAAG]AGAAAGAAAGAAGGA | 55130 |
| rs773805947 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27819285 | AAGGAATGAAAAAGG[A/G]GGAAAGAGAACTTCA | 55130 |
| rs773824838 | in-del | -/GG | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27924005 | AAAGAAAGAAAGAAA[-/GG]GAAAGAAAGAAAGAA | 55130 |
| rs773839132 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27843888 | GGTTTAAACTTGATA[G/T]ACTATAACCACTACT | 55130 |
| rs773839349 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27973267 | CATACGCTGAGACAG[C/T]CAGATCACTTGAAGC | 55130 |
| rs773849825 | snp | A/G/T | 0.000103655 | 0.00719853 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944181 | GCTGTGTGCAGTGGC[A/G/T]GCTGGCACTAGATGA | 55130 |
| rs773853999 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27955219 | AGAATAACTCTGTGC[C/T]ATCACATTCTTTTCC | 55130 |
| rs773855572 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27842216 | TACATGTTTTTGACC[C/T]GTCTCTTCTTAAATG | 55130 |
| rs773876382 | in-del | -/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27866989 | ACTTCTTTTTTTTTT[-/C]CTCAAGAAAACCGGG | 55130 |
| rs773901838 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27899403 | ATTTCAGCAGACACC[C/T]AGCTAGCTGCAGGAG | 55130 |
| rs773902753 | snp | A/C | 0.00224356 | 0.0334178 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944217 | ACAACATCACGGCTA[A/C]TCACCAGTTTGGTGA | 55130 |
| rs773909815 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27862774 | ATTATATATTATTTC[A/T]ACATGTATATGTATA | 55130 |
| rs773920662 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27946910 | CCATTTAAGAAAATT[A/T]CTTCCATGCCTCTAG | 55130 |
| rs773924194 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27889224 | CTAGAGAGATCAAGT[C/T]GGACCCAACCTTCTG | 55130 |
| rs773925519 | in-del | -/AA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27979470 | ACACACACACACACA[-/AA]CAGAGTTAAATGAAT | 55130 |
| rs773935799 | snp | C/T | 8.27041e-05 | 0.00643002 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27944287 | ACTTGGCAACATTCG[C/T]GATAGTCTCGGCTGC | 55130 |
| rs773939155 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27972673 | AAATAATATTAACAG[A/G]GACGAAGAGGAGCAC | 55130 |
| rs773939856 | snp | C/T | 2.31876e-05 | 0.00340489 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27968932 | ACATACCGAAGTAAT[C/T]GTGCTCTTCCGTGTG | 55130 |
| rs773989630 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27887855 | TAAAAAAGTGGGAAG[A/T]CCCAAATAACTAAAA | 55130 |
| rs774028749 | snp | A/C/T | 1.65261e-05 | 0.0028745 | missense, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983895 | CACAGAGTCTCACCA[A/C/T]CGTGAGGTTTCACCA | 55130 |
| rs774032838 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27830231 | TGTCTTTCTCACCAC[A/G]TAACACCTCCCCTTG | 55130 |
| rs774036248 | snp | A/G | 1.71796e-05 | 0.00293079 | intron-variant | ARMC4 | GRCh38.p7 | 10:27862425 | AAAACAAAAAGATGT[A/G]TTACTTACTGTATTT | 55130 |
| rs774043027 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27964467 | TAGTTCTGTATTATC[A/C]GGCATATTCATTCAC | 55130 |
| rs774069311 | snp | A/C | 6.59544e-05 | 0.0057422 | missense, utr-variant-3-prime | ARMC4 | GRCh38.p7 | 10:27936831 | CTGGCCAAGGGCTTA[A/C]GTCCTCCGTGCAGCC | 55130 |
| rs774077317 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27959398 | TCTTTCCCCCAGATG[A/G]CATGCTTTCTAGGAG | 55130 |
| rs774079038 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27919973 | AATGTCAGATAAAAC[A/G]CTCTATGCTTTCATT | 55130 |
| rs774080742 | snp | A/G | 3.52144e-05 | 0.00419594 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27985168 | GTTTTCTTTCATTGT[A/G]TTATAATCAGAGCCC | 55130 |
| rs774082977 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27932322 | TTGAATACTGTACTG[A/C]AATTGAAGAAAAGAA | 55130 |
| rs774096860 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27850306 | AAAAATTAGACGGCC[A/G]TGGTGGCAGGCGCCT | 55130 |
| rs774140910 | in-del | -/GCAG | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27873632 | AGTAGTCATTCAGGA[-/GCAG]GTTGTTCAGTTTCCA | 55130 |
| rs774171095 | in-del | -/AAA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27852961 | ACGAGACACAGTCTC[-/AAA]AAAAAAAAAAAAAAA | 55130 |
| rs774176375 | snp | A/G | 3.40896e-05 | 0.00412839 | intron-variant | ARMC4 | GRCh38.p7 | 10:27961720 | CAGCACTCTTCCTAA[A/G]AACAATAACAACACA | 55130 |
| rs774200174 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27904026 | GTTGCCAAAAAGGGT[A/T]TATGCAGACAACAAT | 55130 |
| rs774225569 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27871102 | GTACTTCTCTGATGG[C/T]CACTGATGATGAGCA | 55130 |
| rs774235207 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27894465 | CCACTGATTAACCTA[C/T]GATATAAAGTTACTG | 55130 |
| rs774248087 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27991110 | GTGTCATTTGTTCTT[A/G]GTTTACAGCAAATTT | 55130 |
| rs774282736 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27957348 | CTAAGGAACCTCGCC[A/C]TCTCCCCTTCACACC | 55130 |
| rs774283333 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27856103 | AGCAAATAACTTGGA[C/T]ATCTCTTAGACTTCT | 55130 |
| rs774313354 | snp | C/T | 1.69152e-05 | 0.00290814 | missense, utr-variant-5-prime, intron-variant | ARMC4 | GRCh38.p7 | 10:27981477 | TTACCAATTTAGACA[C/T]ATTTTCTGAAAATTT | 55130 |
| rs774313479 | in-del | -/TAAATAAC | 0.000179453 | 0.0094707 | intron-variant | ARMC4 | GRCh38.p7 | 10:27853390 | AAATAAATAAATAAA[-/TAAATAAC]TAAAAGTAAGCCCTA | 55130 |
| rs774348881 | in-del | -/ATAGAACAAAAGAAAAATCACCTTATTTATTT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27918398 | TGAGTCACTTTATTA[lengthTooLong]ATAGAACAAAAGAAA | 55130 |
| rs774352367 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27933424 | AGTCACTGAAGGTTT[A/T]GTGGGCCAAGAAAAC | 55130 |
| rs774399473 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27927364 | ACAAGTTCCTAACCC[A/G]TGAATTATGGAAGAT | 55130 |
| rs774402002 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27936266 | ATACTTTAAAATCGA[A/T]TCTGATGAAATCATG | 55130 |
| rs774435557 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27883369 | TAGTTAATAACAAAA[C/T]AAACAATAGCAAAAG | 55130 |
| rs774475189 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27992993 | CAATCTCGGCTCACT[A/G]CAACCTCCACCTCCC | 55130 |
| rs774479547 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27857324 | AATACATAATACATA[C/T]AACATACGAAATATG | 55130 |
| rs774488987 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27852114 | CAAAATAAAAAGTCT[C/T]TTTTAGATATATAAG | 55130 |
| rs774495532 | snp | C/T | 1.64958e-05 | 0.00287187 | synonymous-codon, missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27812584 | ACCAGCTGCAGCTTC[C/T]TGGAGATCCTGGTCA | 55130 |
| rs774498883 | snp | C/T | 4.96545e-05 | 0.00498245 | intron-variant | ARMC4 | GRCh38.p7 | 10:27934978 | TCTCCCTAACACTTA[C/T]ATAAAATCTTTCCAT | 55130 |
| rs774587003 | in-del | -/CA | 1.7277e-05 | 0.00293908 | frameshift-variant, intron-variant | ARMC4 | GRCh38.p7 | 10:27944249 | ACCCCCGTGCTGCCT[-/CA]CCACCCGCCGTGCTC | 55130 |
| rs774587750 | snp | A/C | 1.64727e-05 | 0.00286986 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27812522 | AAATTTCAAGTGTAT[A/C]TTGCCTTCTCTGTAG | 55130 |
| rs774637248 | snp | C/T | 0.000115989 | 0.00761453 | intron-variant | ARMC4 | GRCh38.p7 | 10:27945009 | GGAACACCGCATTCC[C/T]ATAGAAATGCACTAA | 55130 |
| rs774651879 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27941833 | CCTGAAGGTCAACTT[A/C]CACAGATACTGCCCG | 55130 |
| rs774671464 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27902469 | GAACTGAAGGTGATA[C/G]AGACAGGAAAAACTC | 55130 |
| rs774677439 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27890090 | GAGCAAGTACAATGA[C/T]AGATCATGGAACAAA | 55130 |
| rs774706520 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27988815 | TCTGAATCCCCAAAA[C/T]CTATGAACATGTCAC | 55130 |
| rs774713884 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27957589 | CATCATCACCTATGG[C/G]GGAGAAAAGAAGCTG | 55130 |
| rs774716452 | snp | A/G | 2.24338e-05 | 0.00334909 | intron-variant | ARMC4 | GRCh38.p7 | 10:27987551 | TTGTTTCACTAAAAA[A/G]TAAAAATAAAAAATT | 55130 |
| rs774730727 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27901624 | TAGAGGAATCTTTAC[C/T]AAGCAAATGGAAAGC | 55130 |
| rs774734615 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27966286 | GGTCTATTCAAGAAG[C/T]GACTTAAACTTAACT | 55130 |
| rs774748015 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27885909 | TTTATATATAAAAAT[A/T]TATATATATTTTTAT | 55130 |
| rs774756809 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27840532 | TTGGACAAGGGGGTG[G/T]GTACTTTTCTTAAAC | 55130 |
| rs774767397 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27856108 | ATAACTTGGATATCT[C/G]TTAGACTTCTCATAT | 55130 |
| rs774772387 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27877368 | GTGCATGGTATGAGA[C/T]ACCAGGAGCCAAAGT | 55130 |
| rs774789035 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27904189 | AACAATAGCTTTCCA[C/T]GTGATAGGGCTCCTG | 55130 |
| rs774794629 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27909482 | CATCAGCTACTTAGC[C/T]ATAATGAGTGAGGAT | 55130 |
| rs774820185 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27965417 | GCATAGGGTGAGGAT[A/T]TAAGAAAATTCATTT | 55130 |
| rs774898195 | in-del | -/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27938127 | ATTTTTAGTAGAGAT[-/G]GGGGTTTCACCACGT | 55130 |
| rs774902458 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27891312 | AATCATTCTCAAATT[A/C]CTGACTGGCTTCTCA | 55130 |
| rs774971206 | snp | A/G | 0.000318319 | 0.0126118 | synonymous-codon, intron-variant | ARMC4 | GRCh38.p7 | 10:27968943 | TAATTGTGCTCTTCC[A/G]TGTGAAACAGATGGT | 55130 |
| rs774979481 | in-del | -/TT | 3.30131e-05 | 0.00406269 | frameshift-variant | ARMC4 | GRCh38.p7 | 10:27994959 | CTGAGGGCGCCAAAC[-/TT]GTGTTCCATTCAAGT | 55130 |
| rs775055451 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27843597 | ATGATGAAACACCAC[C/T]TATACTAAAAATAGA | 55130 |
| rs775056814 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27889057 | TAGTTTAGATTTTAC[A/G]GGACAATAAAACAAA | 55130 |
| rs775065845 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27821959 | AAAACTAGCCCCCAC[A/G]CTTTTGAAAACTTAA | 55130 |
| rs775090920 | snp | A/C | 1.65932e-05 | 0.00288034 | intron-variant | ARMC4 | GRCh38.p7 | 10:27987379 | CAGACTGGAGCATTA[A/C]GATCACCTTCAACAC | 55130 |
| rs775097676 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27845849 | ACATGATGGTAAAGG[G/T]ATCAATTCAACAAGA | 55130 |
| rs775104383 | snp | C/T | 1.65121e-05 | 0.00287329 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27939981 | TTCAATGATCCTTTC[C/T]GCTTTGATTGCAGCC | 55130 |
| rs775110392 | snp | G/T | | | missense | ARMC4 | GRCh38.p7 | 10:27994976 | GTGTTCCATTCAAGT[G/T]GTTCCACAAAAACAA | 55130 |
| rs775119426 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27953094 | ACCTGTGCAATCATT[A/G]CTACGATGAAAGTAA | 55130 |
| rs775128362 | snp | C/T | 1.69169e-05 | 0.00290829 | utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27995179 | TGAGCTTAGCACACG[C/T]ACTACATCAGAGCAG | 55130 |
| rs775157474 | snp | C/T | 1.66239e-05 | 0.00288299 | missense | ARMC4 | GRCh38.p7 | 10:27862595 | GTTCCAAACCACCAA[C/T]AAAGGAACGAACCAT | 55130 |
| rs775176066 | in-del | -/CATACACACAGATGTATGCATGCATG | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27817067 | TTATGCAGTTTTATA[-/CATACACACAGATGTATGCATGCATG]CATACACACTTTTAT | 55130 |
| rs775194677 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27918892 | ATTCAAAAATTAATT[A/T]TGTATCCATTACTTG | 55130 |
| rs775194756 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27933478 | GGAAAGTAAATTTCA[A/G]TGTTTTCAGGAACAA | 55130 |
| rs775203384 | in-del | -/TTA/TTTTTG | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27941601 | CAGCATCCAGTTTTT[-/TTA/TTTTTG]TTTTTTTTTTTTTTT | 55130 |
| rs775228185 | snp | C/G | 3.29837e-05 | 0.00406088 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27971148 | AGTTTAAGCTTGGTT[C/G]CCATCTCTTGGTCAT | 55130 |
| rs775237399 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27856359 | GGAAATCCTTGTTGA[A/C]CTCTTACCAGTATTT | 55130 |
| rs775237784 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27921478 | TTGTATAAAAGAACA[A/G]TAGAGACTAAATAAC | 55130 |
| rs775255177 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27969986 | TGTCACACACCTGTA[A/T]TCCCAGCTACTCGGG | 55130 |
| rs775273884 | in-del | -/A | 1.65111e-05 | 0.0028732 | intron-variant | ARMC4 | GRCh38.p7 | 10:27981589 | GTTTTGCCCTTTGGG[-/A]AAAAAACAAGTTTCA | 55130 |
| rs775283863 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27818883 | TCCTAGAAAAATCAC[C/T]ATCAAACCATAGTCA | 55130 |
| rs775312616 | snp | C/T | 3.35362e-05 | 0.00409475 | missense | ARMC4 | GRCh38.p7 | 10:27862442 | TACTTACTGTATTTG[C/T]CAGTTTGGACAATAA | 55130 |
| rs775338898 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27881942 | AGGTTGAAGTGGGCA[A/G]ATTGCTTGAGCCCAG | 55130 |
| rs775365330 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27918190 | AGGGCCTGCATAAAC[A/C]TGATACTAACACTTG | 55130 |
| rs775369949 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27868414 | ATTCACAATAGCAAA[A/G]CCATGGAATCAACCC | 55130 |
| rs775371985 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27993246 | TTTAATTTGTTTTAC[A/G]TAGGAGATCATATTT | 55130 |
| rs775378809 | snp | C/G | 1.65012e-05 | 0.00287234 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27812593 | AGCTTCCTGGAGATC[C/G]TGGTCAGGGGACCCA | 55130 |
| rs775416000 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27839033 | GGAGGAATCCTGGAC[C/T]GTTCAATTTAGGCAA | 55130 |
| rs775417493 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27903867 | GAGTTCTATGGTCAC[A/C]CCAAGACAAGGGTGT | 55130 |
| rs775436779 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27941798 | CCATCATCTATGCAC[A/G]TCTACTCCATTCTTC | 55130 |
| rs775462815 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27986526 | CTCGCCTAATAAGGA[A/G]TAATAGGCAAGGCAT | 55130 |
| rs775516338 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983457 | TAGATAAGCCCCTCT[C/T]TTTCCCTTTGTCCCT | 55130 |
| rs775518677 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27915476 | ATTTCATTTATGAGG[C/T]CTCTACCCTCACGTC | 55130 |
| rs775528150 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27838197 | TTCAAGGGAAAAAAC[-/A]AGATATTTTCTGAGT | 55130 |
| rs775537008 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27834706 | AGTGACAGATTTATG[A/G]GTATCTGCTTGCAGA | 55130 |
| rs775537767 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27829906 | GCTTCAGGACTGGCC[C/T]TAAGCAAGGTATTCA | 55130 |
| rs775539105 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27854186 | GATACCATGACATAC[A/C]TGTTAGAATGTCTAA | 55130 |
| rs775541922 | snp | C/G | 5.32231e-05 | 0.00515836 | intron-variant, utr-variant-3-prime | ARMC4 | GRCh38.p7 | 10:27939875 | AAAGAACGCCAACAA[C/G]CGCTGGGAGAGTTCA | 55130 |
| rs775552764 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27960632 | TGGGATTATAGGTGT[A/G]AGCCACTGCACCCTG | 55130 |
| rs775555420 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27852186 | AAGTTAAAAGTCTTC[G/T]AGGCAGAAGGAAAAT | 55130 |
| rs775567146 | snp | G/T | 3.30532e-05 | 0.00406516 | intron-variant | ARMC4 | GRCh38.p7 | 10:27981630 | AACATAAGAACAATT[G/T]TAAGAAGCTGATCAA | 55130 |
| rs775567373 | snp | A/G | 1.65488e-05 | 0.00287647 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944773 | AAGAGAGCCCAGGAA[A/G]GTGGGAACAAGACTC | 55130 |
| rs775571319 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27980467 | TATTGGGTATATACA[A/G]AAACTACAACAACAA | 55130 |
| rs775580292 | snp | C/T | | | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27936406 | ATTCCATGGGAAATC[C/T]GCCCACTCACCTTGA | 55130 |
| rs775581654 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27916650 | TTCACTTCCACTTAA[-/T]GAATAGTAATTATAT | 55130 |
| rs775654977 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27950446 | CCCTGAGGAGAAAGA[A/G]AGAATACTGTTTCCC | 55130 |
| rs775656956 | snp | A/G | 6.8472e-05 | 0.00585076 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983808 | TAACAATCAAAGTCC[A/G]CTGGCTTTAGTTACG | 55130 |
| rs775666126 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27867438 | CATGCACAGAAGAGA[A/C]ACTACACGGAATAGC | 55130 |
| rs775676502 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27902613 | AAAAATGATACAGGG[G/T]AGATCACCACTGATC | 55130 |
| rs775678325 | snp | C/G | 1.64925e-05 | 0.00287158 | missense | ARMC4 | GRCh38.p7 | 10:27940763 | CATACAGACTCGATT[C/G]GGCAGGTTTTGTGGA | 55130 |
| rs775686414 | snp | A/C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27975714 | AAACATTTAATAAAC[A/C/T]GACCAAACATTTAAT | 55130 |
| rs775715120 | in-del | -/TAT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27953382 | TTGTATAGAACTCCC[-/TAT]TACTGCTATCAAAAA | 55130 |
| rs775717890 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27925273 | GGAATAAGAAAAAAA[-/T]CATGATGAAACATAT | 55130 |
| rs775735297 | snp | G/T | | | intron-variant, missense | ARMC4 | GRCh38.p7 | 10:27835994 | ACATTAAGTGGAAGT[G/T]GATCATCATAAAGGT | 55130 |
| rs775736625 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27860945 | CATTAAGACACCAAT[A/G]AGTCTAGAGAAAAGG | 55130 |
| rs775746829 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27822198 | GGTAGCATGGGAATT[C/G]GGTCTGCATTCAATT | 55130 |
| rs775756526 | snp | C/G | 1.65296e-05 | 0.00287481 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27994948 | TGATTCAAATGCTGA[C/G]GGCGCCAAACTTGTG | 55130 |
| rs775828192 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27945246 | GCCTTGAGAGGCTGA[A/C]TGAGGAATGCAAGAT | 55130 |
| rs775832474 | snp | G/T | 0.000265688 | 0.0115227 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984318 | TTTAAAATGTCAGCT[G/T]AAATACTTTAAACAG | 55130 |
| rs775854627 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27957786 | AGCTCATAGCTCTGG[A/G]CGAATAATAAGCTAT | 55130 |
| rs775860790 | snp | C/T | 8.37332e-05 | 0.0064699 | missense, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27961684 | CTGAGGAGCTATCGC[C/T]AACAGTTTCCTCAAT | 55130 |
| rs775867986 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27837756 | AGAATCAAGTGTTTA[C/T]TCCCACAAGTGTATT | 55130 |
| rs775883845 | snp | A/T | 1.66189e-05 | 0.00288256 | stop-gained, utr-variant-5-prime, intron-variant | ARMC4 | GRCh38.p7 | 10:27981509 | GGTGATTTTTCTCTT[A/T]AAAATGTGACAAGGT | 55130 |
| rs775889258 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27861578 | TCCACCCTAGGAATA[C/T]ATTGATATCAGTAAT | 55130 |
| rs775896641 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27910199 | CACTTTTAGAATTTC[C/T]GCAATAGCTCCTTGA | 55130 |
| rs775931645 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27899503 | GGCTGAAGCCAGGGA[A/G]CCAAGTGGTCTAGCT | 55130 |
| rs775976859 | in-del | -/AAAC | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27922931 | AACAAAATAAAACAA[-/AAAC]AAACAAACAAAAAAC | 55130 |
| rs775993229 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27926820 | ATTATGGTCCCCAAA[A/G]CATAAATGTTAATGG | 55130 |
| rs776024531 | in-del | -/A | 3.55783e-05 | 0.00421757 | intron-variant | ARMC4 | GRCh38.p7 | 10:27981416 | ACCATAGAAAGTTGT[-/A]GTTTAGTAACATAAT | 55130 |
| rs776077817 | in-del | -/AAAT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27970105 | TCTGTCTCAAAAAAT[-/AAAT]AAATAAATAAATAAA | 55130 |
| rs776083738 | in-del | -/TTCCC | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27928809 | CAATACTAGCCTACA[-/TTCCC]TTTACACACAGCACT | 55130 |
| rs776092153 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27884952 | AAGGTCTTCCGAGCT[A/G]GTCTGCAAAAACTGA | 55130 |
| rs776106849 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27932486 | AAAGATTAAAAGATG[A/T]TTTGTGATATAGTCT | 55130 |
| rs776117818 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27875722 | TGGGTGCAGCCCACC[A/G]AGCATGAGCCAAAGC | 55130 |
| rs776118157 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27844028 | CACAGCAAGTTCCCA[C/T]CTCTACAAACAATAA | 55130 |
| rs776147159 | snp | C/T | 5.42972e-05 | 0.00521015 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27944239 | GTTTGGTGATACCCC[C/T]GTGCTGCCTCACCAC | 55130 |
| rs776165169 | snp | A/G | 0.000214247 | 0.0103478 | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27936689 | GGTGTTTCAGAAGCC[A/G]TATCTTCATTTCAGA | 55130 |
| rs776171739 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27952220 | TAATACAATGGCTAT[C/T]TGACATATAAAAAAA | 55130 |
| rs776193229 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27862941 | CAGTTGATTCTTACT[A/G]TTTGTGGTAGCTTTG | 55130 |
| rs776201269 | snp | G/T | | | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999276 | GGCGGCAAGTTAGCA[G/T]AAAACTTAAAATGGA | 55130 |
| rs776203658 | snp | C/T | 1.64961e-05 | 0.00287189 | missense | ARMC4 | GRCh38.p7 | 10:27860810 | TACAGCAACGTGAAA[C/T]AGCTTCTGCTAGATG | 55130 |
| rs776211645 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27971944 | TTATTCAGTCAGGAG[-/T]AATACCATGCCAGCC | 55130 |
| rs776234837 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27818283 | ACTTGATCCTTTGAT[G/T]ACATAATTGTATAAC | 55130 |
| rs776237848 | snp | C/G | 1.84252e-05 | 0.00303517 | intron-variant | ARMC4 | GRCh38.p7 | 10:27907631 | ATAGTATTAGAGATT[C/G]TAGAAGAGACTGACT | 55130 |
| rs776257665 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27884046 | AAAAGTTCTCCAAAT[C/T]TGATGAGAAACTTTA | 55130 |
| rs776279454 | in-del | -/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27909683 | TTAGTCAGGCTTGGT[-/G]GGCACGCGCCTGTAG | 55130 |
| rs776288575 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27893937 | GGTGGATCACCTGGA[C/G]CCTGGAGTTTGAGAT | 55130 |
| rs776290212 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27940285 | ATATATAAATGCCAG[C/T]ATATATGTGTGATAT | 55130 |
| rs776293552 | snp | A/G/T | 6.59277e-05 | 0.00574111 | missense | ARMC4 | GRCh38.p7 | 10:27860738 | TTGATTTCAGATAAC[A/G/T]CACTAGTGGAGCCAC | 55130 |
| rs776295149 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27996468 | AAAGGGGGCATTATC[A/G]GCCTTTAGTGTTGAG | 55130 |
| rs776309340 | in-del | -/GG | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27924013 | AAAGAAAGAAAGAAA[-/GG]GAAAGAAAGAAGGAA | 55130 |
| rs776311648 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27870397 | TCTAGGGTACATGTG[A/C]TCAACATGCAGGTTT | 55130 |
| rs776356271 | snp | C/T | 1.64885e-05 | 0.00287123 | missense, intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27971180 | TGATTCCTCCAAAAA[C/T]TAATTTGGTTCTTCT | 55130 |
| rs776382210 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27896126 | TTCATCTCTTTTGAA[C/T]TGACATCTAAAAATG | 55130 |
| rs776388220 | in-del | -/GCTCCACAGGGCCAGT | 1.64841e-05 | 0.00287085 | frameshift-variant | ARMC4 | GRCh38.p7 | 10:27940698 | ATGACTCTTACTGCA[-/GCTCCACAGGGCCAGT]GCCCCACAGCGAGCC | 55130 |
| rs776491745 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27980207 | TTAAGAGCTAAAACT[A/G]TACAATCCTTAGAGG | 55130 |
| rs776514150 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27940910 | TCACCTCCGTCAAAA[A/C]CAAGAATGCTTTAAA | 55130 |
| rs776534831 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27882106 | CCCAGGAGACAGAGG[C/T]TGCATTGAGCCACAA | 55130 |
| rs776553738 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27827299 | GTCATTCACTCTCAT[C/T]ATTTCATGAACTACT | 55130 |
| rs776565189 | in-del | -/AG | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27881111 | AAGATTTTACTCTTC[-/AG]GATTGTTAAAAGGAT | 55130 |
| rs776577350 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27876316 | GGGCAGACTGACACC[C/T]CACACTGCCGGGTAC | 55130 |
| rs776582852 | snp | A/C | 1.65556e-05 | 0.00287707 | missense | ARMC4 | GRCh38.p7 | 10:27987386 | GAGCATTAAGATCAC[A/C]TTCAACACATGCTTG | 55130 |
| rs776584346 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27915951 | AGGTTGTTTTAATGG[C/T]CCACCATGGAGTGTT | 55130 |
| rs776611443 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27907989 | CATGACACAGAAAAC[-/A]AGCTGCTTGATGATT | 55130 |
| rs776615259 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27897315 | AATTCTCTCCTGACA[C/T]CCAGATTCGTGTATT | 55130 |
| rs776635565 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27979953 | ACTCACACTTCCTTA[C/T]GTCAAAACTATTATA | 55130 |
| rs776644400 | snp | C/T | 1.64879e-05 | 0.00287118 | missense | ARMC4 | GRCh38.p7 | 10:27860641 | TTTACTGCACCATTC[C/T]CATGCATGGTGATGC | 55130 |
| rs776670080 | snp | A/G | 1.66643e-05 | 0.0028865 | missense | ARMC4 | GRCh38.p7 | 10:27862604 | CACCAACAAAGGAAC[A/G]AACCATTTCCCCAGC | 55130 |
| rs776675146 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27822539 | CTTTGGACTGTGTCC[A/G]CCTATGGAATGGCTT | 55130 |
| rs776693300 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27836087 | CTTGCTGTCTCAGGG[A/G]TGGCAGAGTCAGAAG | 55130 |
| rs776735420 | in-del | -/AA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27976962 | CGACTAATTTTTGAC[-/AA]AGTTATAAAGGTAAT | 55130 |
| rs776741018 | snp | A/G | 1.65143e-05 | 0.00287348 | missense, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983910 | TCGTGAGGTTTCACC[A/G]GCACATAACAAATTT | 55130 |
| rs776747678 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27814448 | GTTCAAATTGGGTCA[C/T]TGAAGGATGTCTGCC | 55130 |
| rs776749664 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27828689 | TAGAAAACAATTACC[G/T]TGATTATATAAAGAA | 55130 |
| rs776762356 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27878682 | ATTAGAATAGCATGT[C/T]AGAGAAGTGAAAACT | 55130 |
| rs776776552 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27991004 | CCATGTGATTCTGAG[C/T]GCTTATCCAATTTAT | 55130 |
| rs776777065 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27960370 | TATTATTTTGAGATG[A/G]AGTTTTGCTCTTACC | 55130 |
| rs776786720 | snp | A/G | 1.648e-05 | 0.0028705 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27944879 | GCCTCCAACATCTCT[A/G]ATGGCCAACTGGCAG | 55130 |
| rs776813652 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27892781 | CCTGTAATTCATTAC[C/T]GAAGTCTTTGATTCT | 55130 |
| rs776868732 | in-del | -/AC | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27832536 | CACACACACACACAG[-/AC]ACACACACACACACA | 55130 |
| rs776874083 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27823519 | TCTTATCAGTAAAAT[C/T]AGGATTTTTAATAGT | 55130 |
| rs776878651 | snp | C/T | | | downstream-variant-500B, intron-variant | ARMC4 | GRCh38.p7 | 10:27812043 | GTGAAATCAGCACAT[C/T]TCCTTGGAACTCTCC | 55130 |
| rs776879805 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27837158 | CAGCATCTCGGCTGC[C/T]TCTCTGGGTCACAGC | 55130 |
| rs776880220 | snp | A/G | 0.000714796 | 0.0188915 | intron-variant | ARMC4 | GRCh38.p7 | 10:27853392 | AATAAATAAATAAAT[A/G]AAAGTAAGCCCTAAC | 55130 |
| rs776888125 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27957834 | GGGTATTAATGAGCT[C/T]GTTAAATCTTTTTTT | 55130 |
| rs776909582 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27938425 | GTCTACAAGCTGAGG[A/G]GAGAGGCCTCAGAAG | 55130 |
| rs776923141 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27945526 | GACGAAGAAGAAAGC[A/G]AGCTTCACTGTGGTG | 55130 |
| rs776941133 | snp | A/G | 1.64936e-05 | 0.00287168 | intron-variant | ARMC4 | GRCh38.p7 | 10:27935004 | TCCATCTCCAGGGCC[A/G]CTTACATCATACTTT | 55130 |
| rs776982675 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27934239 | CCCAGTTTCGGGTAT[A/G]TCTTTATCAGCAGCA | 55130 |
| rs776983778 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27813028 | CTGATCATGTCACAA[C/T]CTCATTATATCAGTC | 55130 |
| rs776990779 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27970061 | CAGTGAGCCAAGTTT[A/G]TGCCACTGCAGCCTG | 55130 |
| rs776992489 | snp | C/T | 1.64825e-05 | 0.00287071 | missense | ARMC4 | GRCh38.p7 | 10:27935136 | TTCCGGACAATGACT[C/T]GGTTTTCACGTTCTT | 55130 |
| rs776999613 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27927116 | CAATAGAGTTTTACA[A/G]AATCATTGGTTTCAC | 55130 |
| rs777000468 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27825478 | TTTAAGAACTGACAT[A/G]CCTAATACTGAACTC | 55130 |
| rs777001301 | snp | A/C | 1.6836e-05 | 0.00290133 | missense, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27961700 | AACAGTTTCCTCAAT[A/C]TTTTCAGCACTCTTC | 55130 |
| rs777014458 | snp | C/T | 1.71384e-05 | 0.00292727 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940854 | ATCTTAAAAAGAACA[C/T]TTAAGGCATTCTTCA | 55130 |
| rs777018110 | snp | C/T | 1.65302e-05 | 0.00287486 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944787 | AGGTGGGAACAAGAC[C/T]CCGCATCCAAGGTGA | 55130 |
| rs777033435 | in-del | -/TG/TGTG | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27993972 | AAATATATATATATA[-/TG/TGTG]TATGTGTGTGTGTGT | 55130 |
| rs777039068 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27900483 | AATTGACAGAAGTAG[G/T]CTTCAGAAGGTGAGT | 55130 |
| rs777054337 | snp | C/T | 4.95577e-05 | 0.00497759 | missense | ARMC4 | GRCh38.p7 | 10:27940789 | GTGGAATCATGTGCA[C/T]AGTCTAGTAGAGCAA | 55130 |
| rs777112518 | snp | A/G | 1.65056e-05 | 0.00287272 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27995104 | AGTTCCATGTCCGGC[A/G]GCAGTCCACTGCGTC | 55130 |
| rs777116368 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27949017 | ATTACTTCAAATAAA[A/G]TATTTGAAATAAGCA | 55130 |
| rs777147493 | in-del | -/AAATAAAC | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27971003 | AATAAATAAATAAAT[-/AAATAAAC]AAATAAACAAACAAA | 55130 |
| rs777157993 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27947196 | AAAAATCCTCTCTTT[A/G]TAACTGTCAGGTTCA | 55130 |
| rs777223399 | snp | C/T | 1.64838e-05 | 0.00287083 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27944816 | GACAGAGCCACTCAC[C/T]TTACATTTGACTTCA | 55130 |
| rs777230870 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27933606 | GGAAATGCATTCAAA[A/G]AACATCAGAGGTAGT | 55130 |
| rs777241068 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27832137 | TTCAGCTGCAGCAAC[A/G]AATGAGGCTGAGAAG | 55130 |
| rs777241972 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27953914 | CATCAGCAGCCACAA[C/G]CAGACAGCCACACCC | 55130 |
| rs777271075 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27944032 | AATGAGTTTGAAGAT[G/T]TTTTTGTTTTGGACA | 55130 |
| rs777280534 | snp | C/T | 1.65002e-05 | 0.00287225 | missense | ARMC4 | GRCh38.p7 | 10:27939941 | GCAGCTGCTCATTCT[C/T]ACTATTTAGGTTCTT | 55130 |
| rs777306900 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27878286 | GATTGCACAAATAAG[A/G]TGAAAAATATAAAAC | 55130 |
| rs777324730 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27850076 | TTATGATGTCACATC[A/C]TATATTGATGGTGTA | 55130 |
| rs777338601 | snp | G/T | 3.3145e-05 | 0.0040708 | stop-gained, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983870 | TACTCCTCCTGCACT[G/T]CAAGTAATGCACAGA | 55130 |
| rs777349148 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27974799 | TTGGTAATTTGATAG[G/T]AATAGCATTGAATCT | 55130 |
| rs777355839 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27821808 | CCAACTATAAAGACA[A/T]GTTTTAATATTCTAA | 55130 |
| rs777367600 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27892473 | TCTCATTTCACACTC[C/T]GATTTTCCTATCAGA | 55130 |
| rs777429523 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27893721 | CTAAATAGGACAGGG[A/G]CAGTGACGGGGAGAA | 55130 |
| rs777447373 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27835690 | AAGAGAAGTTTAACA[A/G]AGAATAAAATGTTAT | 55130 |
| rs777467911 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27855018 | CCCAGGCAGAGTGGG[A/G]CAGGAGACAGGGATT | 55130 |
| rs777477268 | snp | A/G | 1.6519e-05 | 0.00287388 | intron-variant | ARMC4 | GRCh38.p7 | 10:27981624 | ATGATTAACATAAGA[A/G]CAATTGTAAGAAGCT | 55130 |
| rs777495854 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27909356 | GACAAAATTTCACAA[C/T]TAACTTTAAAACAAG | 55130 |
| rs777515000 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27965927 | CCATTTAAGCCTTCA[C/T]GCTTATATCAATTCA | 55130 |
| rs777532806 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27958526 | TGTTTTTATTTTAAG[A/T]CGTTGAGAGACTTTC | 55130 |
| rs777550207 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27832821 | AGCTCTCGTGGGTTA[C/G]AACTAAACATCTCTT | 55130 |
| rs777554533 | snp | C/T | 4.99671e-05 | 0.00499811 | missense, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27961653 | TGGTCAGGTGGTTCT[C/T]CATCTTCCTCACTTT | 55130 |
| rs777565268 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27879128 | CTGCTTCTCTAGCCT[C/G]ATTTGACATAATTTT | 55130 |
| rs777571534 | snp | A/C | 0.000151125 | 0.00869134 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940833 | ATAAATCCAATGTTC[A/C]TGGAAATCTTAAAAA | 55130 |
| rs777594102 | in-del | -/TGTG | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27940176 | ATTAATATACACATA[-/TGTG]TGTTTGTGTGTGTGT | 55130 |
| rs777599580 | snp | C/T | 1.67309e-05 | 0.00289226 | missense | ARMC4 | GRCh38.p7 | 10:27994923 | AACTGGCTTACCTGA[C/T]AACATAACCTGATTC | 55130 |
| rs777602760 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27976930 | AGTGTTCAGAAATAC[A/G]TTCACAGACAAATGA | 55130 |
| rs777609514 | snp | C/T | 4.94605e-05 | 0.0049727 | missense | ARMC4 | GRCh38.p7 | 10:27940748 | CCACGTCTCTGGCCT[C/T]ATACAGACTCGATTG | 55130 |
| rs777621887 | in-del | -/AAG | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27901750 | AGGGATCAATGCAAC[-/AAG]AAGAGCTAACTGACC | 55130 |
| rs777629169 | snp | C/T | 1.70953e-05 | 0.00292359 | intron-variant | ARMC4 | GRCh38.p7 | 10:27812657 | GGAGAAGAAGGGACA[C/T]AAGAATAAAAACATT | 55130 |
| rs777637867 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27919841 | ATGAGTAAACTTTCC[G/T]GGATGAAGGACATGT | 55130 |
| rs777640473 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27839142 | GTAACATGATGATGT[C/T]AAGAAAAGGAATAAC | 55130 |
| rs777658517 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27840291 | TTGACTCTAAAACAG[C/G]CTAAATAACAGTGTG | 55130 |
| rs777666039 | snp | C/G | 1.69579e-05 | 0.00291182 | intron-variant | ARMC4 | GRCh38.p7 | 10:27907826 | TCATTAGTATGTGAA[C/G]ACAAACATTTTAATG | 55130 |
| rs777675790 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27911964 | AAAATCTCTCCCAAC[A/G]CAAGTACACTCCTCC | 55130 |
| rs777719165 | snp | A/T | 1.64841e-05 | 0.00287085 | missense | ARMC4 | GRCh38.p7 | 10:27935079 | AGAAGAGCTTGGTTT[A/T]TTCCAACAAGGAGGT | 55130 |
| rs777760843 | snp | C/T | 1.651e-05 | 0.0028731 | missense | ARMC4 | GRCh38.p7 | 10:27907710 | ATGCTGCGCTGGCCT[C/T]CACGTCTGGGTGAGG | 55130 |
| rs777769533 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27933251 | TGAGTCCCTGTCTCT[A/G]AAAAACAAACTAAAC | 55130 |
| rs777791989 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27965220 | GTTACACTAGCCTCA[A/T]AGGAAAGGAGGTCTA | 55130 |
| rs777796660 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27888496 | TCTATTCATGTTCTT[C/T]GCCCTCTTTTTAATG | 55130 |
| rs777823712 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27897005 | GGCTACAACCACGAC[C/T]GCCTAATTCCTGTAC | 55130 |
| rs777834950 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27831543 | AATGTAGAGATGAGG[A/G]AACCATGGCATAGAA | 55130 |
| rs777840986 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27837102 | CATATTCATCCTGAG[G/T]GAAAATTTGTTGTCC | 55130 |
| rs777848030 | in-del | -/G | 1.66435e-05 | 0.0028847 | frameshift-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27961639 | TTGCTTCCTGACGAT[-/G]GTCAGGTGGTTCTTC | 55130 |
| rs777912382 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27883213 | TAATGCACACAGAAC[C/G]CTTATCACAGGGTGG | 55130 |
| rs777944135 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27860370 | AGGCAGGAGGATCAC[G/T]TGAGCCCAGGAGTTC | 55130 |
| rs777976048 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27867186 | AAACTAGCAACCACA[A/G]TGGGAAGGCAGAGGC | 55130 |
| rs777992152 | snp | A/C | 1.64988e-05 | 0.00287213 | missense, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984275 | CTTCACCGTCATGGG[A/C]CTTAAACTTATTTCT | 55130 |
| rs777995780 | in-del | -/AAAAAAAAAAAAAAAAAAAAAAAAATATAA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27824140 | GAGACTCCGTCTCAA[lengthTooLong]AAAAAAAAAAAAAAA | 55130 |
| rs778014326 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27950758 | TGCCTGACCCATATG[C/T]ATTCTTTTTAATTTG | 55130 |
| rs778017230 | snp | C/T | 1.67181e-05 | 0.00289115 | intron-variant | ARMC4 | GRCh38.p7 | 10:27935290 | GAGAATTGGTTTTTG[C/T]ATAAGGTTTGCTAAA | 55130 |
| rs778018058 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27978559 | GCACTTTGGGAGGCC[A/G]CGACAGGTGGATCAC | 55130 |
| rs778060750 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27942193 | GCTCCTCACAATCTT[C/T]GCCTTGCAAAAATTT | 55130 |
| rs778074057 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27814979 | TTTCCCTTTCCAATG[A/C]CTATTTTAAATCTTC | 55130 |
| rs778098880 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27888055 | TAATAAAAAGCCTCC[C/T]AACGAAGAAAAGGAC | 55130 |
| rs778099942 | snp | C/T | 1.77439e-05 | 0.00297853 | intron-variant | ARMC4 | GRCh38.p7 | 10:27981431 | AGTTTAGTAACATAA[C/T]GCTATGAAAGCTCAA | 55130 |
| rs778115249 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27907909 | TTTTTTTTTGCAAAA[C/T]TTCATCAACAGTAGG | 55130 |
| rs778141558 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27884286 | ACCCTCATTCTCCTA[C/T]GGAAACATTAAATAA | 55130 |
| rs778145100 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27929612 | TCAAGTAGTTTTTTC[A/G]GGGAGAGCTAGAGAG | 55130 |
| rs778151579 | in-del | -/G | | | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27981862 | GCACTCTGCTGTTCA[-/G]CAGAGAAGTGAGAGC | 55130 |
| rs778179026 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27988726 | TCTGACCAACCGAGA[C/T]TACTTATTACTGACG | 55130 |
| rs778187627 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27851956 | ACATGACATACAGAG[A/G]AACAAACATAAGCAT | 55130 |
| rs778217939 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27825893 | TCTGTTTTTCTAATA[C/T]ATGAATAAAATCATA | 55130 |
| rs778224510 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27818987 | ACCTCTTAACCCAAC[C/T]TTCTCATATGTGTAA | 55130 |
| rs778228068 | snp | G/T | 1.66527e-05 | 0.00288549 | intron-variant | ARMC4 | GRCh38.p7 | 10:27987369 | GTTCAAATCACAGAC[G/T]GGAGCATTAAGATCA | 55130 |
| rs778230640 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27865378 | TTCATGTCCTCAAAT[A/G]TGCATGTCTCCACAA | 55130 |
| rs778265731 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27917442 | TATAATACCAATGAA[C/T]ACAGCTTTTACCTTA | 55130 |
| rs778268232 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27815949 | GAAATTTTTTATTTT[G/T]TCTATATAAACATGA | 55130 |
| rs778326716 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27989741 | TGGTCCCAGCTACTT[G/T]GGAGGCTGAGGTGGG | 55130 |
| rs778338789 | snp | C/G/T | 3.30056e-05 | 0.00406226 | missense | ARMC4 | GRCh38.p7 | 10:27987455 | AGCGTGACAGCTGCC[C/G/T]AAAGCTCCTAATTTT | 55130 |
| rs778348315 | snp | A/G | 1.65362e-05 | 0.00287538 | missense | ARMC4 | GRCh38.p7 | 10:27862573 | GATTTCAGTAAATTG[A/G]CAATAAGTTCCAAAC | 55130 |
| rs778378519 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27912041 | CAGTAAAGTTTTCAT[C/T]TGAAGTTGTCTCTAA | 55130 |
| rs778389473 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27964008 | GAGTGGATTGCTTGA[A/G]GTTGGGAGTTTGAGA | 55130 |
| rs778396983 | snp | C/T | 0.000168569 | 0.0091791 | intron-variant | ARMC4 | GRCh38.p7 | 10:27862666 | TCAAAACTAAACCTA[C/T]ATTTAGGCATTTTTT | 55130 |
| rs778438129 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27928013 | GTTGACATCACCACT[G/T]GGGTGTCCCATAGGA | 55130 |
| rs778438179 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27911199 | CAGACTGTGAAAAAC[A/G]TGGCACTAAACAGAT | 55130 |
| rs778442295 | in-del | -/C | | | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999315 | GAAGCAGAAAATATT[-/C]CTTAGAAACCCCTTT | 55130 |
| rs778461659 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27862334 | GCAATGGGTATTAAA[C/T]TTGAATCCAGGTTTC | 55130 |
| rs778469971 | snp | A/G | 1.6507e-05 | 0.00287284 | missense, intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27971243 | TTGCGGAGGGCAGCT[A/G]CTTCTTCCTTCTTGG | 55130 |
| rs778473407 | snp | A/T | 1.64798e-05 | 0.00287047 | synonymous-codon, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27944945 | CAACGCAATCACTGT[A/T]GCTGTTTGATTTCCT | 55130 |
| rs778504521 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27837973 | ATCTTACCCCACGGC[A/G]ATGGATTGGGAAACA | 55130 |
| rs778512787 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27880231 | TAATCAAGTTGAACA[A/T]TTTTCCTACAAAAGA | 55130 |
| rs778536293 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27985280 | TACAACAAACATTAA[C/G]ACTAATAAATCCTTC | 55130 |
| rs778546942 | snp | G/T | 0.00272851 | 0.0368349 | intron-variant, missense | ARMC4 | GRCh38.p7 | 10:27853277 | GAGGCTGAGGCAGGA[G/T]AATCGCTTGAATCCG | 55130 |
| rs778560005 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27914421 | GTTTTAGCATTCATT[A/G]ATTATCCTTGCCTAA | 55130 |
| rs778572920 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27877261 | TTCTCCAGTTGCTTC[A/T]TCAGTAGAGACAATC | 55130 |
| rs778581107 | snp | A/G | 1.65021e-05 | 0.00287241 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27939960 | ATTTAGGTTCTTGAC[A/G]AGGTTTTCAATGATC | 55130 |
| rs778597841 | in-del | -/A | 3.34969e-05 | 0.00409235 | frameshift-variant | ARMC4 | GRCh38.p7 | 10:27939902 | TTCACTGCACCTGGT[-/A]AATGGCCATGGCGCA | 55130 |
| rs778615773 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27832866 | TTTACTGTGACCTAA[A/G]CAGCTACTGAGAAAA | 55130 |
| rs778651164 | in-del | -/AAAC | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27859840 | TGCACAGATTTAAAC[-/AAAC]AAACAAACAAACAAA | 55130 |
| rs778663550 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27923309 | AAGTGTAGATCAAGA[C/T]ATATCAAGCAAATGG | 55130 |
| rs778668492 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27938238 | GCCACCCAGTACCTC[A/C]GAATGTGACTGTATT | 55130 |
| rs778670888 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27875832 | GGCACCTGGAAAATC[A/G]GGTCACTCCCACCCT | 55130 |
| rs778671524 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27933923 | TTAGACGAAGCCCCC[-/T]GATAGGATTTTGCTG | 55130 |
| rs778671641 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27922344 | AGGGATGAGCTCCAA[A/C]CTAAGACTATAGAAC | 55130 |
| rs778681143 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27899770 | CCTCTCTAGATTCCT[C/T]CTCTCTGGGCAGGGC | 55130 |
| rs778682808 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27933311 | TTGATATTTGCAAGT[A/C]AAAGATGAAAGCAAA | 55130 |
| rs778692040 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27819969 | GTTATGCATTTGAAT[C/T]GCATAGTCCAGTGCC | 55130 |
| rs778697231 | snp | C/T | 3.30322e-05 | 0.00406387 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983994 | TCTGAAACCAATCAT[C/T]AAGCAATTAACAGGA | 55130 |
| rs778698875 | snp | A/G | 1.6525e-05 | 0.00287441 | synonymous-codon, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983894 | GCACAGAGTCTCACC[A/G]TCGTGAGGTTTCACC | 55130 |
| rs778700742 | in-del | -/TA | 4.95733e-05 | 0.00497837 | intron-variant | ARMC4 | GRCh38.p7 | 10:27945000 | AAGGTTAAGGAACAC[-/TA]CGCATTCCCATAGAA | 55130 |
| rs778705973 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27831785 | CATACTCTGTAGTCC[C/T]AGCTGTGTGTCTTTA | 55130 |
| rs778734931 | snp | A/G | 5.15008e-05 | 0.00507422 | | | GRCh38.p7 | 10:27983798 | CATCTACAGCTAACA[A/G]TCAAAGTCCACTGGC | 55130 |
| rs778739875 | snp | A/G | | | | | GRCh38.p7 | 10:27945046 | ACGAATCCATGAACT[A/G]GAAAACATGTCTCTG | 55130 |
| rs778743746 | snp | A/C/T | 1.64923e-05 | 0.00287156 | | | GRCh38.p7 | 10:27935189 | AACCACATTCACAAG[A/C/T]ACTTCTTCAGGCTGA | 55130 |
| rs778776314 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27926560 | TGAAATGTACTATGA[C/T]TATGTAAGATGTTAA | 55130 |
| rs778777989 | snp | C/T | 1.64838e-05 | 0.00287083 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27935102 | AAGGAGGTTCACAAG[C/T]GGTTGAATGCCACCA | 55130 |
| rs778786743 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27901000 | GAAGAACAACCCCAA[A/G]ACACATAATCATCAG | 55130 |
| rs778787706 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27954586 | TCATGTTTCAGTCGT[C/T]AAGTTGATGTGGTAG | 55130 |
| rs778798446 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27828501 | AGGTAACTACAGGTA[A/C]GTTTGTAGGTGTGGG | 55130 |
| rs778819700 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27869979 | AATATTGAGTCAAAA[G/T]GACCTTCAAAGTAAA | 55130 |
| rs778915890 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27933989 | GTTGTGGGAGAGACC[C/T]GGTGGGAGTTAATTG | 55130 |
| rs778919610 | in-del | -/AG | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27924029 | GAAAGAAAGAAGGAA[-/AG]AGAAAGAAAGAAGGA | 55130 |
| rs778926636 | snp | A/G | 3.4437e-05 | 0.00414938 | intron-variant | ARMC4 | GRCh38.p7 | 10:27961752 | ATACACATGTAAGCT[A/G]TAGTGTGGAGATCTA | 55130 |
| rs778930392 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27884566 | TACTTGAGGGACTGG[C/T]TTCTGTTTTATCTGA | 55130 |
| rs778962675 | snp | A/G | 1.64879e-05 | 0.00287118 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27995083 | AGGGGTGATTTCGAG[A/G]ATTCCAGTTCCATGT | 55130 |
| rs778987122 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27994790 | CTGTGTGTCTCTGGT[C/T]TTCATTCCCTGGTTT | 55130 |
| rs778996559 | snp | C/T | 2.15413e-05 | 0.00328179 | missense, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27985043 | TGTTTTAGAGAATGA[C/T]TGAGGAGGTGCAGAT | 55130 |
| rs779013960 | snp | C/T | 1.65726e-05 | 0.00287855 | missense | ARMC4 | GRCh38.p7 | 10:27995133 | TCAATTTCCTCAGAG[C/T]CACACCCATGGGATC | 55130 |
| rs779015420 | snp | C/T | 9.89462e-05 | 0.00703302 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27940758 | GGCCTCATACAGACT[C/T]GATTGGGCAGGTTTT | 55130 |
| rs779015644 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27920989 | GAGTCTTTCATTACA[C/T]GATCACATAACACTG | 55130 |
| rs779058059 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27818677 | GAGGAGAATAGATTG[A/C]TAGCTACAGCAACTC | 55130 |
| rs779070211 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27815055 | AAGATGACCAATAAG[C/G]TCTCCTTCATAAACT | 55130 |
| rs779073319 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27843094 | TAAGGCCACATGTTA[C/T]ATATTCCCTAGAATA | 55130 |
| rs779079545 | snp | G/T | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27982531 | AACCAAAGCAAAATC[G/T]TATTTGTCTACTGCC | 55130 |
| rs779144204 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27906215 | AGATATGAAAAGACA[C/T]TTCTCAAAAGAAGAC | 55130 |
| rs779159478 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27917784 | AGATTATTTTTTTAA[C/T]GGACCATGGTCCTCC | 55130 |
| rs779161864 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27887013 | AAACAGCAAAAATAA[A/G]TGCTTTCCTATACTT | 55130 |
| rs779163824 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27950320 | TGCTCACAGTGAGTG[A/G]TGTATAACCACGTGA | 55130 |
| rs779245508 | snp | C/T | 2.68619e-05 | 0.00366472 | missense | ARMC4 | GRCh38.p7 | 10:27985110 | TTTCACTTTCAGGAT[C/T]ATCATCTCTGGTAAT | 55130 |
| rs779289514 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27938187 | CAGGTTATCCACACA[C/T]CTCGGCCTCCCAAAA | 55130 |
| rs779298278 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27963851 | TCCGGACAACAGACT[C/G]TGGGTTAAATGTCTC | 55130 |
| rs779310146 | snp | G/T | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983575 | AATGAATCAGTGAAG[G/T]GATTACGTTAAAGAC | 55130 |
| rs779339962 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27926345 | AATTATCATACAGAA[C/T]TCAACGGAGCTCATT | 55130 |
| rs779341171 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27829533 | TTTGGAAGGCATATG[C/T]CAAATGTGGTTGTTA | 55130 |
| rs779369492 | snp | A/G | 1.64781e-05 | 0.00287033 | synonymous-codon, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27936776 | TATAGCCCCTGTGAC[A/G]GCAGCTAACCGCTCT | 55130 |
| rs779369913 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27853968 | AGACTAGCTACAGAC[A/G]GGGAGAAAATATTTG | 55130 |
| rs779399253 | in-del | -/TATATATATA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27827380 | TACACACACACACAC[-/TATATATATA]TATATATATATATAT | 55130 |
| rs779423547 | snp | G/T | 8.26235e-05 | 0.00642689 | missense, utr-variant-3-prime | ARMC4 | GRCh38.p7 | 10:27936867 | AGGTCCCGGGTTTCC[G/T]TATCTTCAGCACACT | 55130 |
| rs779426903 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27987128 | TTTCAAACCACATGC[-/T]AAAATCAGAAACCTA | 55130 |
| rs779439789 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27992256 | AAAGATATCAATAAC[A/G]GTCAGACACAAAAAG | 55130 |
| rs779465353 | snp | C/T | 6.6749e-05 | 0.00577668 | intron-variant | ARMC4 | GRCh38.p7 | 10:27971363 | ATCTGAATTATCTAG[C/T]GTTCTCTGAAGATTA | 55130 |
| rs779472528 | snp | C/T | 1.91753e-05 | 0.00309633 | intron-variant | ARMC4 | GRCh38.p7 | 10:27994887 | TATGTACAACGAAGA[C/T]ATCAAATCCTAGAAG | 55130 |
| rs779512417 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27889638 | TCCCTCAGTCCCACT[A/G]TCCCACATTCTGATC | 55130 |
| rs779516952 | in-del | -/AAAGAAAGAA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27923999 | AAGAAAGAAAGAAAG[-/AAAGAAAGAA]AGAAAGAAAGAAAGA | 55130 |
| rs779518134 | snp | A/G | 1.64923e-05 | 0.00287156 | synonymous-codon, intron-variant | ARMC4 | GRCh38.p7 | 10:27944357 | CACCATAATTGGTAA[A/G]CCCCCAAGGTCAACA | 55130 |
| rs779542392 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27823088 | GGTCAGGGAATTGTG[C/G]GACATTGCTCAGCAC | 55130 |
| rs779573645 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27813649 | ATAAGCAAAGAAATC[G/T]TACTAAGAAAAATAT | 55130 |
| rs779586970 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27900426 | CAAAGGATCATAACT[C/T]CTCACCAGCAAAGGA | 55130 |
| rs779610761 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27851339 | GATTCTTAGAACAAA[C/G]CTCGGGAATATTTAT | 55130 |
| rs779614963 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27986684 | TCCAATAAAGCAGGA[C/T]GCATACATTATCACC | 55130 |
| rs779637564 | snp | C/T | 0.000115377 | 0.00759443 | missense | ARMC4 | GRCh38.p7 | 10:27940601 | TCCCCACCACTGGAA[C/T]TAGCATGTTTTCATG | 55130 |
| rs779662113 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27913824 | CTATTATGAAAAAGT[A/C]AAAAAATAACAGATG | 55130 |
| rs779674180 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27947045 | AGTTCAGAATGACAA[G/T]AGCCTTAATTTTACT | 55130 |
| rs779677574 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27937793 | CGTGATTTTCAATTC[C/T]GGATTACAGGCACCT | 55130 |
| rs779699429 | in-del | -/AG | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27923957 | TAATGAAAGAAAGAA[-/AG]AAAGAAAGAAAGAAA | 55130 |
| rs779705785 | snp | C/T | 1.65064e-05 | 0.00287279 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27987474 | GCTCCTAATTTTAAT[C/T]TGTGGTACAGAGAGA | 55130 |
| rs779716336 | snp | C/G | | | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:28000618 | GTCCAATGTGGATGC[C/G]AGCCAGAGATCTTCC | 55130 |
| rs779763756 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27961345 | TGCCCACTTCCCAGC[C/T]GGGAGAGAGGGTTGG | 55130 |
| rs779766954 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27954673 | ATTGTCTTTACGCTG[C/G]TTTTTCTCCACACAT | 55130 |
| rs779786996 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27909104 | AGTCATACTGCCTTC[C/T]ATATGCTACTTAAAA | 55130 |
| rs779792803 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27832959 | AAGTCGAAGGATATA[C/T]GAGGAAAGCATCAGT | 55130 |
| rs779807117 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27872904 | TTCCCTCTTTTTCTA[C/T]TGATTGGAATAGTTT | 55130 |
| rs779816706 | snp | A/G | | | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27959045 | TTCATCTTCTGAAAG[A/G]CTATGTCTTGGACGG | 55130 |
| rs779818237 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27898582 | GATTAAGATTATCCT[C/T]CAAGGATTTGTATCA | 55130 |
| rs779819331 | snp | G/T | 1.85537e-05 | 0.00304574 | intron-variant | ARMC4 | GRCh38.p7 | 10:27907627 | CAGTATAGTATTAGA[G/T]ATTCTAGAAGAGACT | 55130 |
| rs779831641 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27972549 | ATTTTATATATAAAG[A/T]TACAAATACATCAGA | 55130 |
| rs779853144 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27890746 | CCCCTTATGTCCCCA[C/T]TTGAAAATCTGGTAT | 55130 |
| rs779859624 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27934085 | AGTTTTAAAAAGAAG[G/T]TTCCCTGCACAAGCT | 55130 |
| rs779865743 | in-del | -/GTCTT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27945566 | CTGGCTGAACGCAGA[-/GTCTT]GCAAACCAATGTCTT | 55130 |
| rs779874199 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27876713 | CACAGGTCACACCAA[A/G]GAATGGCAAAATAGA | 55130 |
| rs779882420 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27989103 | AGCCTCCGGAAGGAA[A/T]GCAACCCTGCCGATA | 55130 |
| rs779882822 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27907799 | TGGAACCCAAAATCA[C/T]GATATAAACTGTCAT | 55130 |
| rs779909405 | snp | G/T | 1.67248e-05 | 0.00289173 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940517 | AACTTTTGGACTAAA[G/T]AAAGTCAAGTTGAGA | 55130 |
| rs779911895 | snp | C/T | 1.6504e-05 | 0.00287258 | missense | ARMC4 | GRCh38.p7 | 10:27860626 | TCATTCAACTGTACC[C/T]TTACTGCACCATTCT | 55130 |
| rs779947025 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27942427 | GGAACTTAATTCTTG[C/T]TTATATCAGTTAGTC | 55130 |
| rs779957902 | snp | A/G | 1.64871e-05 | 0.00287111 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944970 | TTTCCTCCCTACAAA[A/G]ATGCAATGCCAGAGA | 55130 |
| rs779972286 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27849153 | ACTTGGAACCAACCT[-/A]AATATTCATCAATGA | 55130 |
| rs779986232 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27858951 | TGGGACTACAGGTGC[A/C]TGCCTATACATTTTT | 55130 |
| rs780003125 | in-del | -/AAAAAAAAAAG | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27921301 | CCCCACCTCCAACGA[-/AAAAAAAAAAG]AAAAAAAAAAGAACA | 55130 |
| rs780020023 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27844388 | CAAACTCTCTGCCAA[C/G]TCCCCTTCCTTTTTG | 55130 |
| rs780020756 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27821329 | TTACTCATTGCTTTG[G/T]TATACACCCAGAGGG | 55130 |
| rs780037655 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27922672 | GCACTTTGGAAGGCC[A/G]AGGTGGGTGGATCAT | 55130 |
| rs780057616 | snp | C/T | 1.64819e-05 | 0.00287066 | missense | ARMC4 | GRCh38.p7 | 10:27935116 | GTGGTTGAATGCCAC[C/T]ACATTTCCGGACAAT | 55130 |
| rs780112130 | snp | C/T | 3.30126e-05 | 0.00406266 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27935219 | ATCTGTTAGAAGTCC[C/T]ACCAAGGTTTCAATG | 55130 |
| rs780148642 | in-del | -/ACT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27963605 | TTTTCCCCCCACTGG[-/ACT]TAACTTGTTGCTAAG | 55130 |
| rs780150735 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27932845 | TGAATGTATAGTCAA[C/T]GTTCCACACATATAA | 55130 |
| rs780176932 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27887572 | CAGGATAGACCATAT[A/T]TGAAGCCGCAAAACA | 55130 |
| rs780182278 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27906085 | TGAACAGGCAACCTA[C/T]AGAATGGGAAAAATT | 55130 |
| rs780183115 | snp | C/T | | | intron-variant, missense | ARMC4 | GRCh38.p7 | 10:27858207 | ACCCAGTATGCCACA[C/T]CCACATTTTTTTCCT | 55130 |
| rs780220531 | snp | C/T | 2.92129e-05 | 0.00382172 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27985126 | ATCATCTCTGGTAAT[C/T]TTGCCAAGAATATTT | 55130 |
| rs780251974 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27992533 | GTCTCTACAAAAAAA[C/T]AGAAAAATTGACCAG | 55130 |
| rs780254116 | in-del | -/T | 1.64795e-05 | 0.00287045 | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27936708 | CTTCATTTCAGAATA[-/T]TGAGAGCCTTCTCTT | 55130 |
| rs780296977 | snp | A/C | 3.4013e-05 | 0.00412376 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940848 | ATGGAAATCTTAAAA[A/C]GAACATTTAAGGCAT | 55130 |
| rs780304619 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27938393 | AGACGGTGGGAGGAC[A/G]CAGGGAAAAGGCAGC | 55130 |
| rs780332725 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27906178 | TTATAAGAAAAAACA[A/T]CTCCATCAAAAAGTG | 55130 |
| rs780341777 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27840194 | TCTGTACATTTTTTT[A/C]TATTTTTATTGATCT | 55130 |
| rs780364348 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27956433 | GCAAGTACTCAGGAA[A/T]AAGACCGCCTGGATG | 55130 |
| rs780365978 | snp | C/T | 4.99388e-05 | 0.00499669 | intron-variant | ARMC4 | GRCh38.p7 | 10:27971060 | GAAAAATTAGGTGAG[C/T]ATGGTTACTAATGCT | 55130 |
| rs780384503 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27869639 | CCCTAGGTTCAAATG[A/T]TTCTCCTGGCTTAGC | 55130 |
| rs780400239 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27812865 | TCCCCACTTTCTCTG[C/G]GTATCTAACTGCTAT | 55130 |
| rs780425658 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27856952 | AGCCTGGACGACAAG[A/C]CCGAAACTCCGTCCC | 55130 |
| rs780443914 | in-del | -/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27819848 | TAAAAAAAAAAAAAA[-/G]GAAAGAAAAAAATAC | 55130 |
| rs780452229 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27953512 | CTGCAGTATTGTTTG[C/T]AGTAACAAAAACTGA | 55130 |
| rs780454920 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27951449 | AGAAACAAACTCTCA[C/T]GTGTGAGACTGCAGA | 55130 |
| rs780479394 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27817485 | TAGGTAATTTTTTAA[A/C]CCTCATTCCCCCTCC | 55130 |
| rs780488257 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27825365 | TCAGAATGTAATAAA[A/C]CCTTTCTTTCTCTTC | 55130 |
| rs780488418 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27894056 | AGGCTGAGGCAGCAG[G/T]ATTGCTTGAGCCCAG | 55130 |
| rs780489486 | in-del | -/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27973923 | GTATTCCCTTTTTTT[-/C]CTGCAACTTCACCAG | 55130 |
| rs780497229 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27912444 | AAGATGCAGCTGTTT[A/G]CTACGTTTCTCAGGC | 55130 |
| rs780532511 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27880418 | GTTTTCAAGACAGTG[G/T]TTCTCAAATTTTACT | 55130 |
| rs780537276 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27932658 | TATGTTCATGCAAGC[C/T]GCCTCCTTCTCAGTT | 55130 |
| rs780542761 | snp | C/G | 1.75946e-05 | 0.00296598 | intron-variant | ARMC4 | GRCh38.p7 | 10:27862391 | ACTACACCATGATAT[C/G]TCAGGACAATATGCA | 55130 |
| rs780571698 | snp | G/T | 3.30104e-05 | 0.00406252 | missense | ARMC4 | GRCh38.p7 | 10:27862537 | GCAGCACATACACTT[G/T]CCAGAACTTCTTTGT | 55130 |
| rs780572433 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27929102 | TGTAAAGGTGACATA[C/T]ATTAATCATGTAGAC | 55130 |
| rs780580645 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27959953 | GTAAAAACAATGTGC[A/G]CCTGATATAGAAATT | 55130 |
| rs780584844 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27826683 | CCCTCATGCTCTGCA[A/T]CCTCCTGCCTCCCTC | 55130 |
| rs780627015 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27956769 | ACGTGTTTTTGACCT[G/T]GGATCCACAAATTCT | 55130 |
| rs780633899 | snp | C/T | 2.15785e-05 | 0.00328463 | synonymous-codon, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27985054 | ATGATTGAGGAGGTG[C/T]AGATCCAATTGCTTA | 55130 |
| rs780653169 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27881340 | CATTGTACTGTATAT[C/T]CAATGCCACTTTAAA | 55130 |
| rs780668501 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27828853 | GCCAAACTGAGAATT[A/C]TCTAAATTATACCCA | 55130 |
| rs780676975 | snp | C/T | 1.65647e-05 | 0.00287786 | missense, utr-variant-3-prime | ARMC4 | GRCh38.p7 | 10:27936877 | TTTCCTTATCTTCAG[C/T]ACACTGCACGAAAAG | 55130 |
| rs780677138 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27890886 | TGAAAATGACAACTG[A/T]CCCCAAACAGGGAGG | 55130 |
| rs780693270 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27834292 | GCTCTGCCACTTTCA[C/T]TGTGTTGGCCAATCT | 55130 |
| rs780697353 | in-del | -/T | 1.64996e-05 | 0.0028722 | frameshift-variant | ARMC4 | GRCh38.p7 | 10:27987443 | AATAAGTAACAAGCG[-/T]TGACAGCTGCCCAAA | 55130 |
| rs780772377 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27835147 | TCCCACCAGCAGGCC[C/G]TTGGAGGAGCGTCAA | 55130 |
| rs780786845 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27843766 | GCAATACTCTGTCTC[-/A]AAAAAAAAACAAAAC | 55130 |
| rs780805514 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27902111 | AACAAACAGTCTCTC[A/G]GACCACAGTGCAATC | 55130 |
| rs780821955 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27936070 | GACTTCACTACGCCT[C/T]ATTAAGTAAACTTAT | 55130 |
| rs780822363 | snp | A/T | 1.71953e-05 | 0.00293212 | intron-variant | ARMC4 | GRCh38.p7 | 10:27994909 | TCCTAGAAGCAAGTA[A/T]CTGGCTTACCTGACA | 55130 |
| rs780837000 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27872736 | GGATAAGCTTTTTGA[G/T]GTGCTGCTGGATTCA | 55130 |
| rs780871590 | snp | A/T | 1.77833e-05 | 0.00298183 | intron-variant | ARMC4 | GRCh38.p7 | 10:27981423 | AAAGTTGTAGTTTAG[A/T]AACATAATGCTATGA | 55130 |
| rs780878255 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27851559 | TAAAACACACTAGAT[A/G]GCAATAAAGGCAAAT | 55130 |
| rs780882563 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27855400 | GTAGTATATATTCAT[C/T]GATACCAATTGGTTC | 55130 |
| rs780896390 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27988662 | ATATTTTGAATTGCA[A/G]TGTAGATACATAGAT | 55130 |
| rs780911721 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27922912 | CTCTGTCTCAAAAAA[C/T]AAAAACAAAATAAAA | 55130 |
| rs780911890 | in-del | -/AT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27935842 | CACACATATGTATGC[-/AT]ATATATATATACACA | 55130 |
| rs780945863 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27944546 | AAGAAATCATTTCCA[C/T]TCCCAGAGGTTACAC | 55130 |
| rs780949745 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27986151 | CTTCACTGGGGGAGA[A/G]GAGAGCAGCGAAAAG | 55130 |
| rs780962751 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27820382 | CCCAAACTCTTGATC[C/T]AGTTACATAATTTCC | 55130 |
| rs780963538 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27944804 | CGCATCCAAGGTGAC[A/G]GAGCCACTCACCTTA | 55130 |
| rs780967136 | snp | A/G | 1.65113e-05 | 0.00287322 | utr-variant-3-prime, intron-variant | ARMC4 | GRCh38.p7 | 10:27812490 | ATGTAGAATTTGATA[A/G]CTTGTAATGTCCATT | 55130 |
| rs780978575 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983704 | TGGATTTGCCCAGCA[A/G]GCATATATCAAAGGA | 55130 |
| rs780980740 | snp | A/G | 4.94735e-05 | 0.00497336 | missense, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984267 | ATATCCTTCTTCACC[A/G]TCATGGGACTTAAAC | 55130 |
| rs780985159 | snp | A/G | | | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27857885 | CAGGAATGTTTGTAC[A/G]ACTGGAAAATAACAA | 55130 |
| rs780989521 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997641 | GCAATGCACAAGTTT[C/T]ATTCAAGAAGGTTGG | 55130 |
| rs780996336 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27877719 | TCTTAAAAACCTAGT[C/T]GTTGCCAGTTTCACC | 55130 |
| rs781009850 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27977985 | GTTGCTTAAACATAC[A/G]ACTACCATATGATCT | 55130 |
| rs781019118 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27989582 | ATACCAAGCTACTTA[A/C]CTAGAGAGAGTGAAA | 55130 |
| rs781020264 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27861286 | CGTGAGCCACTGCAC[A/C]CAGCTGAAGGAACTA | 55130 |
| rs781039930 | snp | A/G | 1.69625e-05 | 0.00291221 | intron-variant | ARMC4 | GRCh38.p7 | 10:27961536 | GTATTTTAAATGAAC[A/G]TTGCAAACATACTAC | 55130 |
| rs781041842 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27879536 | TAATTCCCTGTTCAG[A/G]TTCAGACAGATGCTT | 55130 |
| rs781050141 | in-del | -/CT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27814576 | AGTCTGACCTCCAAA[-/CT]CTCTGACCACAATGT | 55130 |
| rs781058039 | snp | A/T | 5.01626e-05 | 0.00500787 | intron-variant | ARMC4 | GRCh38.p7 | 10:27907807 | AAAATCATGATATAA[A/T]CTGTCATTAGTATGT | 55130 |
| rs781094685 | snp | C/T | 3.2962e-05 | 0.00405954 | missense | ARMC4 | GRCh38.p7 | 10:27940624 | TTTTCATGAGAAGTC[C/T]TCAGCAGCCGAGCCA | 55130 |
| rs781095447 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27818582 | CTAATCCTATACTAA[C/G]AGCTTGATTTCCATA | 55130 |
| rs781117876 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27857186 | TTCAGCCTACTCTAC[A/G]TGAAGATGACAAGGA | 55130 |
| rs781120231 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27884693 | GGGAGACTGCAGACT[C/G]ACAGACACCTGGGGG | 55130 |
| rs781121421 | in-del | -/AAAT | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997720 | ATCAATGTTATTAGA[-/AAAT]AAATAAATAAATAAA | 55130 |
| rs781123116 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27910896 | GTATATATAAAGTGG[A/G]TTCCCGTGAGCCTCT | 55130 |
| rs781123560 | in-del | -/TTAAGTT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27915540 | TTCTCACAATGGGGA[-/TTAAGTT]TCAACATCTAAATGT | 55130 |
| rs781149711 | snp | A/C | 1.64825e-05 | 0.00287071 | stop-gained | ARMC4 | GRCh38.p7 | 10:27940733 | CACAGCGAGCCACTT[A/C]CACGTCTCTGGCCTC | 55130 |
| rs781161766 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27869821 | ATTACAGGCATGAGC[A/C]ACCATGCCTGGCCGA | 55130 |
| rs781176912 | in-del | -/TAAT | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27982483 | TTGTCCCTTTATTCC[-/TAAT]TAGAGATTTCGTTTT | 55130 |
| rs781181211 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27909252 | TGATATTTAACTGTA[C/T]ATTGCTGGACAGAAA | 55130 |
| rs781186466 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27841487 | TGCAACCTCCACCTC[C/T]CAGGTTCAAGCAATT | 55130 |
| rs781189804 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27952790 | AGGTTGAAGGTCCAG[A/G]GTTGAAAACTATTGG | 55130 |
| rs781190850 | in-del | -/TTTTTTTTTTTTTTTTTTTTTTTTATTTTTTTTTTGTCGTTTGTTT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27948782 | TTGGCCTTTGGATTT[lengthTooLong]TTTTTTTTTTTTTTT | 55130 |
| rs781198362 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27943899 | TTTCAGCATTCCACC[A/G]AGCAGCAGGTCTCAC | 55130 |
| rs781228941 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27843425 | AGCAACTGGCTGATG[C/T]AGAGTGGCTCTACAT | 55130 |
| rs781229178 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27982772 | AATTTATGTTGAAGA[C/T]ACTGAGGGCAGGATG | 55130 |
| rs781262758 | snp | A/G | 6.59881e-05 | 0.00574367 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944986 | ATGCAATGCCAGAGA[A/G]AGGTTAAGGAACACC | 55130 |
| rs781267876 | snp | A/G | 1.6563e-05 | 0.00287771 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984023 | GAGTTCCTTAACCTA[A/G]AGTTTGGTAAAAAGT | 55130 |
| rs781273325 | in-del | -/AATT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27836784 | ATAATAATTACTATC[-/AATT]GATTGATTAATAATG | 55130 |
| rs781286186 | snp | C/G | 4.99463e-05 | 0.00499707 | intron-variant | ARMC4 | GRCh38.p7 | 10:27935277 | TCATAAGAAAGAGGA[C/G]AATTGGTTTTTGTAT | 55130 |
| rs781294210 | in-del | -/AGA | 0.000185293 | 0.00962352 | intron-variant | ARMC4 | GRCh38.p7 | 10:27812644 | TCACACATAAGGAGG[-/AGA]AGAAGGGACACAAGA | 55130 |
| rs781326915 | in-del | -/AAAAAAAAAAAAA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27885510 | GTGAGACTCCATCTC[-/AAAAAAAAAAAAA]AAAAAAAAAAAATAT | 55130 |
| rs781343344 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27980982 | TACATAAACAAAATA[A/T]TATTCTACCATAAAA | 55130 |
| rs781424449 | in-del | -/GC | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27848543 | ACAATGGTAACAAAA[-/GC]CAAAATTGACAAATG | 55130 |
| rs781430977 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27838763 | ACTTTATTTTACCAT[A/T]CTGTTTGTGTATTTT | 55130 |
| rs781435721 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27896908 | GAAAAAACTATGAAT[C/T]CTTTTTTCCTCTATT | 55130 |
| rs781461205 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27979550 | TCTGATTTGATCACT[C/G]AAAAGCTGTATTTCT | 55130 |
| rs781472150 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27978830 | CTGAATAGAAGGCAA[C/T]TTCCTCAACATGCTA | 55130 |
| rs781481807 | snp | C/G | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27960227 | TAGGAGCCTGCCAAA[C/G]AGATCTCCAAGTTGA | 55130 |
| rs781516128 | snp | A/G | 0.000117303 | 0.00765753 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27944260 | GCCTCACCACCCGCC[A/G]TGCTCTTTTAAACTT | 55130 |
| rs781540426 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27941145 | TAGCTTCCCTAAAAC[C/G]ATTAGCACTTTCTAA | 55130 |
| rs781568192 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27962134 | CTCTATTGCAGGTGC[-/A]ATTGCTCTGGGTGCA | 55130 |
| rs781570988 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27939714 | TTGCCCTCCAGCCTG[C/G]GCAACAGAGCAAGAC | 55130 |
| rs781571021 | in-del | -/AACAT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27919818 | AATAAAATTGGTTGA[-/AACAT]AACATGAGTAAACTT | 55130 |
| rs781601948 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27892490 | ATTTTCCTATCAGAT[-/A]ATGAATGGACCGATA | 55130 |
| rs781621808 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27891687 | CTTAATAAAAACTTT[C/T]AAAAACTCATTAATG | 55130 |
| rs781633507 | snp | A/C | 1.65913e-05 | 0.00288017 | intron-variant | ARMC4 | GRCh38.p7 | 10:27971083 | CTAATGCTGCATCTG[A/C]AAACAAATGCAAATA | 55130 |
| rs781639928 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27881658 | ACACTGAAAAGAATG[A/G]GCCGGCAAAAATACA | 55130 |
| rs781643559 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27814736 | GCATAGTCCGTCTTT[C/T]GAATCATTCTCTTAT | 55130 |
| rs781651341 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27949020 | ACTTCAAATAAAATA[G/T]TTGAAATAAGCAAGT | 55130 |
| rs781687456 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27910783 | AACAAACAAACAAAC[-/A]AAAAAAACAGATACA | 55130 |
| rs781694882 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27915181 | AATGGCTGAAACCCA[A/C]AGGTAAAAAGCCAAT | 55130 |
| rs781697726 | in-del | -/AA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27852962 | CGAGACACAGTCTCA[-/AA]AAAAAAAAAAAAAAA | 55130 |
| rs781732280 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27929222 | GGATATCTCTGTATG[A/T]CTTTAGGTAGATAGA | 55130 |
| rs781757781 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27852004 | CTAAAACAATGCAGG[C/T]GATAATAAAATGGAG | 55130 |
| rs781759392 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27825810 | ATGGAAAGCAGAAAG[A/T]GACTTGAGCCAATGT | 55130 |
| rs781763033 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27986975 | TTTAAAGGAAATAGA[C/T]TGTCATTCAATCTAT | 55130 |
| rs781767977 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27930538 | AAAACAGGCTGAGAG[A/C]ATGGCGTGAACCCGG | 55130 |
| rs781779525 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27865210 | ATACCCTGAGCCAGT[A/G]GCTCTCTATGTGAGC | 55130 |
| rs781781620 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27822749 | GTCAGTGAAGGGAGT[C/T]AAGGGGCTTGCCTTT | 55130 |
| rs781782128 | snp | C/T | 3.30316e-05 | 0.00406383 | missense | ARMC4 | GRCh38.p7 | 10:27862552 | GCCAGAACTTCTTTG[C/T]TATCTGATTTCAGTA | 55130 |
| rs796067514 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27863197 | GGAGCTTATTTAACA[C/T]AGATATTTTCTCTTT | 55130 |
| rs796083803 | multinucleotide-polymorphism | AA/GG | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27924007 | AGAAAGAAAGAAAGA[AA/GG]GAAAGAAAGAAAGAA | 55130 |
| rs796088776 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27906367 | CAGGAAACAACAGAT[A/G]CTGGAGAGGATGTGG | 55130 |
| rs796100591 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27819590 | AAAAAAAAAAAAAAA[A/T]AAAAAAAAAAAGTTA | 55130 |
| rs796107496 | in-del | -/AT | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27982164 | TTCTTCCATAACAGA[-/AT]ATATATATATAATGT | 55130 |
| rs796125080 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27964141 | GTAGGAGAAGCACTT[A/G]AACCTGGAAGGCAGA | 55130 |
| rs796127523 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27943657 | CCGGGCTTGATGGCG[A/G]GCACCTGTAGTCTCA | 55130 |
| rs796129388 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27969787 | ATATCACCTACAGGC[C/T]GCAACTTGTAAACTA | 55130 |
| rs796150802 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27834297 | GCCACTTTCATTGTG[C/T]TGGCCAATCTCAATG | 55130 |
| rs796161934 | in-del | -/TT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27820778 | ATGAAGCCCAGCAAC[-/TT]TTTTTTTTTTTTTTT | 55130 |
| rs796181950 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27987936 | ATGTTATTTTATTTA[C/T]AAAATTTTTACACCA | 55130 |
| rs796184171 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27818019 | CCACATCCACCATGG[C/T]AACCTTTGTTATCCT | 55130 |
| rs796190885 | in-del | -/TGAATGAATGAATGAA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27954496 | ATGAATAAACACGAG[-/TGAATGAATGAATGAA]TGAATGAATGAATGA | 55130 |
| rs796194806 | in-del | -/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27928064 | CCATAACTGAACTCA[-/C]CATTCATTTATTATA | 55130 |
| rs796218912 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27852662 | AATAACAAGATGGTA[C/T]ATTTAAAGCTAACCG | 55130 |
| rs796230981 | snp | C/T | | | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999615 | CCACCTCTAGACACC[C/T]TACCAGCAAGAGCCC | 55130 |
| rs796243799 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27965712 | TTATTGACACCCTAC[A/G]CAGTGCAAACCTGGA | 55130 |
| rs796289397 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27890199 | ATGGGGTCACAGTGC[-/A]ATGGGAGTGCTTAAG | 55130 |
| rs796313360 | snp | C/T | | | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27857917 | CATTTGACGAGAAGT[C/T]GGCAGCAGGAATTAG | 55130 |
| rs796321141 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27835938 | ATCAAAAAAAAAAAA[-/A]GGAAAAGAAAATCAT | 55130 |
| rs796323318 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27954999 | TTCAAACAAGCAATT[-/A]AAAAAAAGTCACAAA | 55130 |
| rs796326232 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27934133 | CCACCATGTAAGATG[C/T]GACTTGCTCCTCCTT | 55130 |
| rs796420434 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27894861 | TGAGCCACTTTGCCC[A/G]GCTTCAAATGAAATT | 55130 |
| rs796429089 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27941282 | TGAGGCCAGGAATTA[A/G]AGACCAGCCTGAACA | 55130 |
| rs796429186 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27827390 | CACACTATATATATA[C/T]ATATATATATATATA | 55130 |
| rs796433394 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27969826 | GCTTTAAAAAGTGGG[C/T]TGGGTGCAGTGGCTC | 55130 |
| rs796439556 | in-del | -/TTTC | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27893560 | CAAACAAAGACGTTA[-/TTTC]TTTCAAAGTGATGCC | 55130 |
| rs796461531 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27870460 | GCTGCACCCATTAAC[G/T]CGTCATTTACATTAG | 55130 |
| rs796464361 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27937339 | TTTCTTTCTTTTTTC[-/T]TTTTTTTTTTTTTTT | 55130 |
| rs796470409 | in-del | -/AA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27852979 | AAAAAAAAAAAAAAA[-/AA]GAAAAGCTAACCGTG | 55130 |
| rs796480079 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27925913 | TGGGAGGCTGAGACA[C/G]GAGAATTGCTTGAGC | 55130 |
| rs796486035 | in-del | -/AG | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27979472 | CACACACACACACAC[-/AG]AGTTAAATGAATTCA | 55130 |
| rs796516555 | in-del | -/AAACA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27854767 | TCACAAAACAAAACT[-/AAACA]AAACAAAAAAAGAAA | 55130 |
| rs796520253 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27817528 | TTTTGGGGTCTCCAA[C/T]GTCTATTATTCCATG | 55130 |
| rs796529233 | in-del | -/AG | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27924049 | AAGAAAGAAGGAAAG[-/AG]AAAGAAAGAAAGAAA | 55130 |
| rs796535585 | multinucleotide-polymorphism | AGG/GGT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27889488 | CAGTAAGAAAGCTGG[AGG/GGT]GCCAGGCTGGAAAAT | 55130 |
| rs796551242 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27901802 | TACAGGAGCACCCAG[A/T]TTCATAAAACAATTC | 55130 |
| rs796627547 | in-del | -/AA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27890784 | TTTAAAAAAAAAAAA[-/AA]CTTGTATTATCATTC | 55130 |
| rs796632517 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27957933 | TCTCTGCTAGCTTAA[A/G]TCTACATTTAAGCCA | 55130 |
| rs796647500 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27931169 | CTATGCTTCGAATGA[C/G]CATGACACTTATTTG | 55130 |
| rs796661245 | multinucleotide-polymorphism | CA/TG | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27946743 | ACAAGCTTCCCACAC[CA/TG]CTCCTCCTTCTTATG | 55130 |
| rs796702144 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27881976 | TTCGAGACCAGACTC[A/G]ACAACATGGTGAAAC | 55130 |
| rs796736885 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27970823 | ACAAAAAATAAAAAG[C/T]TAGCCAGGCGTGGTG | 55130 |
| rs796768276 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27850041 | AATGGACACAGCACT[A/G]AAGTGAATATTACAA | 55130 |
| rs796783925 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27852112 | ACAAAATAAAAAGTC[-/T]TTTTTTAGATATATA | 55130 |
| rs796802479 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27963962 | CATGGTGGCTCACGC[C/T]TGTAATCCCAGCACT | 55130 |
| rs796837290 | in-del | -/TAAA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27971007 | AAATAAATAAATAAA[-/TAAA]CAAACAAACAAAATA | 55130 |
| rs796858979 | in-del | -/AAAAAAAAAA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27909818 | GTGAGTCTTCATTTG[-/AAAAAAAAAA]AAAAAAAAAAAAAAA | 55130 |
| rs796882490 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27821621 | AAAGTGCAGTTCGTG[C/T]TTTCAAATCACTAAC | 55130 |
| rs796888641 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27817356 | AATTCTTTTCAAAAA[G/T]TTTGGATATATTTCG | 55130 |
| rs796896824 | multinucleotide-polymorphism | AT/GC | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27969811 | AAACTATTTGTTAAG[AT/GC]TTAAAAAGTGGGCTG | 55130 |
| rs796941708 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27844199 | ACCCTGTCTCAAACC[-/A]AAAAAAAAGAATAAT | 55130 |
| rs796942952 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27948461 | CAAAGGATTTTTGAA[C/T]GTTTGTTCCACTTTG | 55130 |
| rs796946401 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27989180 | AACTGTAAGATAATA[C/T]ATTTGTGTGTGTTAA | 55130 |
| rs796952928 | multinucleotide-polymorphism | AAA/CAG | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27969516 | CACTTGCCAGTTAAA[AAA/CAG]GTTGCCCATGCATTT | 55130 |
| rs796953243 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27903404 | CAAGACAAGGATGCC[C/T]TCTCTCACCACTGCT | 55130 |
| rs796988824 | multinucleotide-polymorphism | AA/GC | | | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:28000449 | GCATCACACCTGTGG[AA/GC]GTAATGCAGGTCACA | 55130 |
| rs796994904 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27966874 | AAATCTGGATATTGT[A/G]TATAAAACAAACATA | 55130 |
| rs796996467 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27972276 | GCTAAGAAACTTTTA[A/G]TAAGAAATATAACTA | 55130 |
| rs796999198 | multinucleotide-polymorphism | AC/TA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27827380 | ACACACACACACACT[AC/TA]ATATATATATATATA | 55130 |
| rs797000248 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27916516 | GTGTGGGACCACTTA[-/A]CATGTGGGTTTCCTT | 55130 |