| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs200517 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27872320 | tcaattaggaaaaga[C/G]gaagtcaaattgtcc | 55130 |
| rs200518 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27872033 | ctacaaaccactgct[C/T]aaggaaataaaagag | 55130 |
| rs394249 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27872822 | gcagagacacaacca[A/T]aaaagagaattttag | 55130 |
| rs880706 | snp | G/T | 0.462363 | 0.131916 | intron-variant | ARMC4 | GRCh38.p7 | 10:27904958 | CACAAACAATATTTA[G/T]GTTAAAGGACTTAAG | 55130 |
| rs880707 | snp | G/T | 0.463126 | 0.13068 | intron-variant | ARMC4 | GRCh38.p7 | 10:27904011 | AAATAAGGACTACCT[G/T]TTGCCAAAAAGGGTA | 55130 |
| rs880708 | snp | C/T | 0.463126 | 0.13068 | intron-variant | ARMC4 | GRCh38.p7 | 10:27904103 | ACTCCCCAAACTGTT[C/T]CCTCATACAGAATGA | 55130 |
| rs915174 | snp | C/T | 0.437542 | 0.165312 | intron-variant | ARMC4 | GRCh38.p7 | 10:27844600 | GGGCAAGTTATTTAA[C/T]CTTTATGAAACTCAA | 55130 |
| rs915175 | snp | C/T | 0.444 | 0.157683 | intron-variant | ARMC4 | GRCh38.p7 | 10:27844758 | AAAACGATATGACTT[C/T]CATTATTATCTAGCT | 55130 |
| rs933065 | snp | A/C | 0.452842 | 0.146134 | intron-variant | ARMC4 | GRCh38.p7 | 10:27949394 | GAGCTGTGGAAGCAC[A/C]TCACAGGGAACTTTG | 55130 |
| rs952403 | snp | A/G | 0.113685 | 0.209567 | intron-variant | ARMC4 | GRCh38.p7 | 10:27825215 | agtgatggtaatggg[A/G]agatgtcaggacaga | 55130 |
| rs952404 | snp | C/T | 0.154661 | 0.231107 | intron-variant | ARMC4 | GRCh38.p7 | 10:27825192 | aggacagattctggg[C/T]ttattttgaaggtaa | 55130 |
| rs983258 | snp | C/T | 0.166832 | 0.235761 | intron-variant | ARMC4 | GRCh38.p7 | 10:27939088 | ATCTACACTAACTTT[C/T]TGTGTATGATACATT | 55130 |
| rs1041661 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | ARMC4 | GRCh38.p7 | 10:27877435 | ATAAGCTTCCTAATG[A/G]CTCCTAATCTGTGGG | 55130 |
| rs1061577 | snp | A/G | 0.106278 | 0.204558 | utr-variant-3-prime, intron-variant | ARMC4 | GRCh38.p7 | 10:27812382 | AATGAAAACACACAA[A/G]TTGAAAATGCACAGA | 55130 |
| rs1090967 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27872779 | gatgaacatcaatgc[A/C]aaaatcctcaataaa | 55130 |
| rs1090968 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27872750 | aaatactggcaaacc[A/G]aatccagcagcacat | 55130 |
| rs1095911 | snp | C/T | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872504 | ccaaaataataagag[C/T]tatgtatgacaaacc | 55130 |
| rs1319351 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | ARMC4 | GRCh38.p7 | 10:27884194 | actcaaacaagggaa[C/T]ctcattaagctcaac | 55130 |
| rs1334719 | snp | A/C | 0.462144 | 0.132269 | intron-variant | ARMC4 | GRCh38.p7 | 10:27894494 | TGATAAAACAAATAT[A/C]TGGGGAGCTATGCTA | 55130 |
| rs1334720 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ARMC4 | GRCh38.p7 | 10:27894637 | GCTTGAGTGCAGTGG[C/T]GCAATCACGCCTCAC | 55130 |
| rs1334721 | snp | G/T | 0.0490535 | 0.14873 | intron-variant | ARMC4 | GRCh38.p7 | 10:27866708 | ggaagcaagagaggg[G/T]agggaggtgccagac | 55130 |
| rs1413772 | snp | C/T | 0.462582 | 0.131564 | intron-variant | ARMC4 | GRCh38.p7 | 10:27897177 | CACCCGCCTGCCTTC[C/T]TTCTTTACTTCActc | 55130 |
| rs1419366 | snp | A/G | 0.485731 | 0.0832509 | intron-variant | ARMC4 | GRCh38.p7 | 10:27931024 | TGAGGCATCAGAAGT[A/G]GAGCCTTGGGAAAAG | 55130 |
| rs1547327 | snp | C/G | 0.437542 | 0.165312 | intron-variant | ARMC4 | GRCh38.p7 | 10:27856511 | TAGATATTTCCCAGG[C/G]CTCTCTAAACTCTCT | 55130 |
| rs1556641 | snp | A/G | 0.49706 | 0.0382258 | intron-variant | ARMC4 | GRCh38.p7 | 10:27877047 | ACTCAGTGAACATTC[A/G]AAAATATTTGTTGAA | 55130 |
| rs1556642 | snp | A/G | 0.499853 | 0.008585 | intron-variant | ARMC4 | GRCh38.p7 | 10:27877568 | TTTTAAACATATGAC[A/G]TCTTGCCTCGCATAG | 55130 |
| rs1812592 | snp | C/T | 0.437542 | 0.165312 | intron-variant | ARMC4 | GRCh38.p7 | 10:27845260 | gaagagagtgggggc[C/T]gatattcaacattct | 55130 |
| rs1832003 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27949089 | AGCAAATGTTTATTT[C/T]TTCCTTATCAATGGT | 55130 |
| rs1832004 | snp | A/C | 0.462472 | 0.13174 | intron-variant | ARMC4 | GRCh38.p7 | 10:27900223 | cttctaacagtcagg[A/C]ctctctgctgcaggt | 55130 |
| rs1832005 | snp | C/T | 0.462472 | 0.13174 | intron-variant | ARMC4 | GRCh38.p7 | 10:27900438 | ttccagttttgttcc[C/T]ttgctggtgaggagt | 55130 |
| rs1832006 | snp | G/T | 0.217851 | 0.247924 | intron-variant | ARMC4 | GRCh38.p7 | 10:27900525 | TGGGTTAGAACATGC[G/T]CCTTTAGCTCAGACG | 55130 |
| rs1833058 | snp | C/G | 0.454784 | 0.1434 | intron-variant | ARMC4 | GRCh38.p7 | 10:27966397 | CAAGCTCCTGGAGTT[C/G]AGGGCAGAGTGAATT | 55130 |
| rs1857616 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27920271 | CATTATTCACTTTCC[C/T]TTATGTATAGTTTAC | 55130 |
| rs1857617 | snp | A/C | 0.497121 | 0.0378299 | intron-variant | ARMC4 | GRCh38.p7 | 10:27883064 | TCCTGGGAATCTAAA[A/C]GGCTACATACATGTG | 55130 |
| rs1889522 | snp | C/T | 0.437542 | 0.165312 | | | GRCh38.p7 | 10:27853909 | agcagaagtttttaa[C/T]gctggtgaagtccaa | 55130 |
| rs1889523 | snp | C/G | 0.49703 | 0.0384237 | | | GRCh38.p7 | 10:27844532 | TGGTGGTTCAGAGAG[C/G]AGCCTCTAAACCCAC | 55130 |
| rs1892115 | snp | A/G | 0 | 0 | | | GRCh38.p7 | 10:27965022 | GCTTGATGGACAGGA[A/G]GCAACAGTCAGTAAG | 55130 |
| rs1931888 | snp | C/T | 0.392511 | 0.205404 | intron-variant | ARMC4 | GRCh38.p7 | 10:27818128 | CAGCCTGGATGCCAA[C/T]GGATCCTGATATTCA | 55130 |
| rs1931889 | snp | C/T | 0.451856 | 0.147493 | intron-variant | ARMC4 | GRCh38.p7 | 10:27946744 | ATAAGAAGGAGGAGG[C/T]GTGTGGGAAGCTTGT | 55130 |
| rs1931890 | snp | A/C/G | 0.00676848 | 0.0578101 | intron-variant | ARMC4 | GRCh38.p7 | 10:27921046 | TGTTTACTTTACAAC[A/C/G]TGTGGAAGGAAAATA | 55130 |
| rs1931891 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27921252 | gtgacccctcatcat[C/G]ccactgtactttagc | 55130 |
| rs1962094 | snp | A/T | 0.451732 | 0.147663 | intron-variant | ARMC4 | GRCh38.p7 | 10:27963710 | ctacagaaatgctca[A/T]gtttttgattacagg | 55130 |
| rs1963750 | snp | C/G | 0.111224 | 0.207945 | intron-variant | ARMC4 | GRCh38.p7 | 10:27841445 | ctgtcacctaggctg[C/G]agtgcagtggtgcga | 55130 |
| rs1963751 | snp | A/C | 0.498774 | 0.02473 | intron-variant | ARMC4 | GRCh38.p7 | 10:27841474 | gatctcagctcactg[A/C]aacctccacctccca | 55130 |
| rs1964950 | snp | C/T | 0.499653 | 0.0131743 | intron-variant | ARMC4 | GRCh38.p7 | 10:27841437 | gtcttgctctgtcac[C/T]taggctggagtgcag | 55130 |
| rs1970631 | snp | C/T | 0.494358 | 0.0528145 | intron-variant | ARMC4 | GRCh38.p7 | 10:27942806 | AAATATGTAATAAAA[C/T]GAATGTGGCAGAATG | 55130 |
| rs1974220 | snp | G/T | 0.498794 | 0.0245311 | intron-variant | ARMC4 | GRCh38.p7 | 10:27845194 | GGGTTACACACAAAG[G/T]GAAGCCCATCAGACT | 55130 |
| rs1974221 | snp | G/T | 0.498794 | 0.0245311 | intron-variant | ARMC4 | GRCh38.p7 | 10:27845217 | ATCAGACTAACAGAG[G/T]ATCTCTTGGCAGAAA | 55130 |
| rs2003191 | snp | C/G | 0.311369 | 0.242351 | intron-variant | ARMC4 | GRCh38.p7 | 10:27904730 | ATGGAAAATAAACAT[C/G]TCGGAATAGCCAGGG | 55130 |
| rs2003192 | snp | C/T | 0.49999 | 0.00219646 | intron-variant | ARMC4 | GRCh38.p7 | 10:27903943 | ATCTCCTCTTCCTCC[C/T]CTCTGGGGTTCCCTT | 55130 |
| rs2065687 | snp | C/T | 0.497121 | 0.0378299 | intron-variant | ARMC4 | GRCh38.p7 | 10:27864586 | GGTGAGAATGGGGAG[C/T]GAGGTGAGAGTGGGG | 55130 |
| rs2065688 | snp | C/T | 0.497151 | 0.037632 | intron-variant | ARMC4 | GRCh38.p7 | 10:27864782 | TACTTGGCTCTATCA[C/T]TTTCTCAAATAATAA | 55130 |
| rs2065689 | snp | G/T | 0.309648 | 0.24278 | intron-variant | ARMC4 | GRCh38.p7 | 10:27821715 | TGTACCAAATTTGTA[G/T]TTCACTTTCCTGAGA | 55130 |
| rs2065690 | snp | A/G | 0.463989 | 0.129263 | intron-variant | ARMC4 | GRCh38.p7 | 10:27898823 | gtgtgaTTCCAGTAA[A/G]GATTTGAGATCTTTT | 55130 |
| rs2152016 | snp | C/T | 0.218151 | 0.247963 | intron-variant | ARMC4 | GRCh38.p7 | 10:27899714 | AGCTGTGGTGGGCTC[C/T]GCCCAGTTCGAACTT | 55130 |
| rs2152018 | snp | C/G | 0.449091 | 0.151204 | intron-variant | ARMC4 | GRCh38.p7 | 10:27867445 | GGATGATGCTATTCC[C/G]TGTAGTTTCTCTTCT | 55130 |
| rs2152019 | snp | A/G | 0.448836 | 0.15154 | intron-variant | ARMC4 | GRCh38.p7 | 10:27867356 | CAGGCCTAACAGAAC[A/G]CCCCAGCACCATCAG | 55130 |
| rs2184418 | snp | A/C | 0.463343 | 0.130326 | intron-variant | ARMC4 | GRCh38.p7 | 10:27899420 | GGGGTATGAAAAAAA[A/C]ACTCCTGCAGCTAGC | 55130 |
| rs2184419 | snp | A/C | 0.141934 | 0.225437 | intron-variant | ARMC4 | GRCh38.p7 | 10:27924951 | caaagcccaggtagt[A/C]ccattgctcaataaa | 55130 |
| rs2225713 | snp | A/G | 0.0973687 | 0.197999 | intron-variant | ARMC4 | GRCh38.p7 | 10:27844258 | GCAAGAGCAGCAAAG[A/G]AGGTTGGAAAATTGC | 55130 |
| rs2297646 | snp | A/C | 0.447291 | 0.153545 | intron-variant | ARMC4 | GRCh38.p7 | 10:27936968 | CTAGAAAGAAGTTTC[A/C]TAGCTACTAGAATGG | 55130 |
| rs2368265 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | ARMC4 | GRCh38.p7 | 10:27845345 | atctgtaaaggattt[C/T]atttctccttcactt | 55130 |
| rs2368266 | snp | A/G | 0.484561 | 0.0864924 | intron-variant | ARMC4 | GRCh38.p7 | 10:27855401 | TAGTATATATTCATC[A/G]ATACCAATTGGTTCT | 55130 |
| rs2368267 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | ARMC4 | GRCh38.p7 | 10:27860217 | aacactttgggaggc[C/T]gaagcaggaggatca | 55130 |
| rs2368268 | snp | A/C | 0.489142 | 0.0728777 | intron-variant | ARMC4 | GRCh38.p7 | 10:27951296 | gatctagaatgaaaa[A/C]tccaaaaaataagtt | 55130 |
| rs2368269 | snp | G/T | 0.442926 | 0.158996 | intron-variant | ARMC4 | GRCh38.p7 | 10:27889490 | AGTAAGAAAGCTGGG[G/T]GGCCAGGCTGGAAAA | 55130 |
| rs2368270 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | ARMC4 | GRCh38.p7 | 10:27901543 | aaagatcaagaccca[C/T]cggtgtgctgtattc | 55130 |
| rs2368271 | snp | C/G | 0.462691 | 0.131387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27901570 | attcaggagacccat[C/G]ttacgtgcaaagaca | 55130 |
| rs2368272 | snp | A/G | 0.493748 | 0.0555599 | intron-variant | ARMC4 | GRCh38.p7 | 10:27901649 | gaaagcaaaaaaagc[A/G]ggggttgcaatccta | 55130 |
| rs2368273 | snp | A/T | 0.493748 | 0.0555599 | intron-variant | ARMC4 | GRCh38.p7 | 10:27901816 | GATTCATAAAACAAT[A/T]CTTGGAGACCTACAA | 55130 |
| rs2368274 | snp | G/T | 0.312348 | 0.242101 | intron-variant | ARMC4 | GRCh38.p7 | 10:27904347 | GGCAGGAAGCAGAGC[G/T]GGAATCTTGGGCTGA | 55130 |
| rs2368286 | snp | G/T | 0.411242 | 0.191052 | intron-variant | ARMC4 | GRCh38.p7 | 10:27970647 | GAAAAATATTGAATA[G/T]ATATTTACATGTCCC | 55130 |
| rs2368288 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27963108 | AGGCAGGAGAATCAC[A/T]TGAACCCGGCAGGCG | 55130 |
| rs2554077 | snp | A/C | | | | | GRCh38.p7 | 10:27872581 | agaaaaggcctttga[A/C]aacattcaacagctc | 55130 |
| rs2815507 | snp | G/T | 0.404035 | 0.196909 | downstream-variant-500B, intron-variant | ARMC4 | GRCh38.p7 | 10:27811674 | GATAAAATGCTATTT[G/T]TTTTGTAGCCACTTT | 55130 |
| rs2887205 | snp | C/G | 0.49706 | 0.0382258 | intron-variant | ARMC4 | GRCh38.p7 | 10:27845526 | TGATGTTAGCTGGTT[C/G]TTTTGCTTGTTAGTT | 55130 |
| rs2887206 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | ARMC4 | GRCh38.p7 | 10:27864490 | tgcaaattagagagt[A/G]aggagtgaagtgaga | 55130 |
| rs2887210 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27972811 | gagagttttgaagtc[A/T]accaattatggattt | 55130 |
| rs2991935 | snp | A/G | 0.499683 | 0.0125759 | intron-variant | ARMC4 | GRCh38.p7 | 10:27828993 | TATTAGAAGAAATTC[A/G]AAACCAAAGACAAGC | 55130 |
| rs2991936 | snp | A/G | 0.10237 | 0.201756 | intron-variant | ARMC4 | GRCh38.p7 | 10:27867817 | ggattacaggttcac[A/G]ccaccatgcccagct | 55130 |
| rs2991937 | snp | A/G | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27849440 | TCATTTACATTAGGT[A/G]TATCTCCTAATGCTA | 55130 |
| rs2991938 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27875632 | agtgatgcagaagac[A/G]ggtgatttctgcatt | 55130 |
| rs2991939 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ARMC4 | GRCh38.p7 | 10:27875733 | caccgagcatgagcc[A/G]aagcagggcaaggca | 55130 |
| rs3004196 | snp | A/T | 0.0283406 | 0.115616 | intron-variant | ARMC4 | GRCh38.p7 | 10:27849616 | CTTTTTAAGTTTTCC[A/T]TGGGGAGCTCTAGGC | 55130 |
| rs3004197 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | ARMC4 | GRCh38.p7 | 10:27829029 | ATGAATTCTATATCC[A/C]ATCATGTATTTTAAA | 55130 |
| rs3060459 | in-del | -/CCTTC/TC | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27873252 | GATTCTTCTCTCTTC[-/CCTTC/TC]TTTATTAGTCTGGCT | 55130 |
| rs3221658 | microsatellite | (CA)19/21/22/23 | 0.480984 | 0.203874 | intron-variant | ARMC4 | GRCh38.p7 | 10:27979431 | naaaacctaaGAATA[(CA)19/21/22/23]AGAGNTAAATGAAAT | 55130 |
| rs3737184 | snp | A/C | 0.090938 | 0.192871 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27812526 | TTCAAGTGTATCTTG[A/C]CTTCTCTGTAGCAAG | 55130 |
| rs3802517 | snp | A/T | 0.475259 | 0.108435 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944540 | TTTTTTAAGAAATCA[A/T]TTCCATTCCCAGAGG | 55130 |
| rs3808909 | snp | A/G | 0.341506 | 0.232651 | intron-variant | ARMC4 | GRCh38.p7 | 10:27987344 | TTTCCCAGCAAGATT[A/G]TTTCTAAAAGTTCAA | 55130 |
| rs3824590 | snp | A/C | 0.482645 | 0.0917714 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944191 | GTGGCGGCTGGCACT[A/C]GATGACGATGACAAC | 55130 |
| rs3831254 | in-del | -/A | 0.143622 | 0.226238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27856272 | TAAATGTGTTAATCA[-/A]TCCCCTCCAATACAG | 55130 |
| rs3839908 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27907889 | ATATTTTGCTTAGAA[-/T]TTTTTTTTTTTTTGC | 55130 |
| rs3897931 | snp | A/G | 0.490727 | 0.0674567 | intron-variant | ARMC4 | GRCh38.p7 | 10:27885297 | tgggcagatcacgag[A/G]tcaagagatcgaaac | 55130 |
| rs3901839 | snp | C/T | 0.497121 | 0.0378299 | intron-variant | ARMC4 | GRCh38.p7 | 10:27869182 | GATTATCCATTATCT[C/T]TATTTGTTCTTGTGC | 55130 |
| rs3902895 | snp | A/G | 0.45762 | 0.139261 | intron-variant | ARMC4 | GRCh38.p7 | 10:27964783 | ACACTACAAGAAAAC[A/G]CAGAAATAAAAATTT | 55130 |
| rs3952837 | snp | C/T | 0.461259 | 0.133677 | intron-variant | ARMC4 | GRCh38.p7 | 10:27962768 | TCCGGCGGTGGGAGG[C/T]GGAGACAAGCTGGTG | 55130 |
| rs4237386 | snp | G/T | 0.492435 | 0.0610346 | intron-variant | ARMC4 | GRCh38.p7 | 10:27926811 | TATCAGAAAATTATG[G/T]TCCCCAAAACATAAA | 55130 |
| rs4237388 | snp | A/G | 0.454302 | 0.144085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27965422 | GGGTGAGGATATAAG[A/G]AAATTCATTTCCTTG | 55130 |
| rs4262624 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27971525 | AAACTCACACCTCTG[C/T]TGCAGCACAACAGAT | 55130 |
| rs4265508 | snp | A/T | 0.485324 | 0.0843964 | intron-variant | ARMC4 | GRCh38.p7 | 10:27917581 | aataaagtcaaaagt[A/T]ggttcttttaaaagg | 55130 |
| rs4303140 | snp | C/T | 0.494187 | 0.0535994 | intron-variant | ARMC4 | GRCh38.p7 | 10:27962740 | GGTCCCTCATGCACA[C/T]GCACACTCATCACAC | 55130 |
| rs4367844 | snp | C/T | 0.330249 | 0.23677 | intron-variant | ARMC4 | GRCh38.p7 | 10:27955150 | CTACTGGAGTTGATT[C/T]GAGTGGACGAACAGT | 55130 |
| rs4382805 | snp | A/G | 0.0577344 | 0.159793 | intron-variant | ARMC4 | GRCh38.p7 | 10:27847157 | gaggatttttgcatc[A/G]atgttcatcagggat | 55130 |
| rs4385792 | snp | C/T | 0.499683 | 0.0125759 | intron-variant | ARMC4 | GRCh38.p7 | 10:27995475 | GGCATAAAACCCAAA[C/T]AGAAAACTCCAAGAG | 55130 |
| rs4387252 | snp | A/C | 0.0926964 | 0.194308 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27996972 | ACACTATCAATATTT[A/C]AAACTATATTAAATA | 55130 |
| rs4405206 | snp | A/G | 0.157661 | 0.232322 | missense, intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27971222 | TTGTCTGAACCAGAA[A/G]TGTCTTTGCGGAGGG | 55130 |
| rs4411816 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27873046 | ttgaatctctgaata[A/G/T]accaataacaagctc | 55130 |
| rs4420169 | snp | C/T | 0.493748 | 0.0555599 | intron-variant | ARMC4 | GRCh38.p7 | 10:27899752 | gccactgtagacaga[C/T]tgcctctctagattc | 55130 |
| rs4469787 | snp | G/T | 0.444133 | 0.157519 | intron-variant | ARMC4 | GRCh38.p7 | 10:27847205 | gataagctttttgag[G/T]tgctgctggattcag | 55130 |
| rs4489649 | snp | A/G | 0.452597 | 0.146474 | intron-variant | ARMC4 | GRCh38.p7 | 10:27961346 | GCCCACTTCCCAGCC[A/G]GGAGAGAGGGTTGGT | 55130 |
| rs4494226 | snp | C/T | 0.4941 | 0.0539917 | intron-variant | ARMC4 | GRCh38.p7 | 10:27953563 | TTATCAATAAGGCAA[C/T]TGTTCAATAACTTAA | 55130 |
| rs4514313 | snp | A/C | 0.49706 | 0.0382258 | intron-variant | ARMC4 | GRCh38.p7 | 10:27847476 | tgcttcatttttgcc[A/C]attcaggatgatatt | 55130 |
| rs4579844 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARMC4 | GRCh38.p7 | 10:27988413 | cgtgatctcgggtca[C/T]tgcaacctctgcctc | 55130 |
| rs4590766 | snp | C/T | 0.485187 | 0.0847778 | intron-variant | ARMC4 | GRCh38.p7 | 10:27958762 | AATATTCTTAATAAT[C/T]CTAATATAAGAGAAC | 55130 |
| rs4600119 | snp | A/G | 0.494484 | 0.0522255 | intron-variant | ARMC4 | GRCh38.p7 | 10:27953972 | CACAGCCCTGCGAGA[A/G]AAATCTCAAAGGCCA | 55130 |
| rs4601670 | snp | C/G | 0.0926964 | 0.194308 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997058 | TATATGCTATAAAAA[C/G]CAAGTACTGGATCAG | 55130 |
| rs4628591 | snp | C/G | 0.485664 | 0.0834419 | intron-variant | ARMC4 | GRCh38.p7 | 10:27943004 | AGGTATTTATTAACC[C/G]TTCATACGGGTAAGG | 55130 |
| rs4694144 | snp | G/T | 0.444444 | 0.157135 | intron-variant | ARMC4 | GRCh38.p7 | 10:27873147 | TTTATTTGCATAGAG[G/T]TGTTTATACTATTCT | 55130 |
| rs4747606 | snp | A/C | 0.490997 | 0.0664859 | intron-variant | ARMC4 | GRCh38.p7 | 10:27875250 | ttattctagttagcc[A/C]ttcatctaatctttt | 55130 |
| rs4747607 | snp | A/G | 0.49706 | 0.0382258 | intron-variant | ARMC4 | GRCh38.p7 | 10:27875387 | gtccagctttgttcc[A/G]ttgctggagaggagc | 55130 |
| rs4747608 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27884310 | TAAATAAACAACTAC[A/T]GACTGACTCAATTTT | 55130 |
| rs4749261 | snp | C/T | 0.499722 | 0.0117779 | intron-variant | ARMC4 | GRCh38.p7 | 10:27824604 | aatggactaaaacCC[C/T]ACAGGTAAGCAAAGA | 55130 |
| rs4749262 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27829667 | CTCTGAAAAAGCCCC[C/G]TAATAATCCCCTAAC | 55130 |
| rs4749263 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARMC4 | GRCh38.p7 | 10:27829726 | GTCTTTTTGCTAAAA[C/T]GTTATAAAATGATGC | 55130 |
| rs4749264 | snp | C/T | 0.495596 | 0.0467178 | intron-variant | ARMC4 | GRCh38.p7 | 10:27837151 | AAGACACCAGCATCT[C/T]GGCTGCCTCTCTGGG | 55130 |
| rs4749266 | snp | C/T | 0.492188 | 0.0620098 | intron-variant | ARMC4 | GRCh38.p7 | 10:27863805 | AATCACCTTCTCTCT[C/T]GCTGTCAGATCTGTG | 55130 |
| rs4749267 | snp | C/G | 0.448708 | 0.151707 | intron-variant | ARMC4 | GRCh38.p7 | 10:27863801 | ACCTTCTCTCTCGCT[C/G]TCAGATCTGTGCAAC | 55130 |
| rs4749268 | snp | C/T | 0.49703 | 0.0384237 | intron-variant | ARMC4 | GRCh38.p7 | 10:27847433 | gtcataaatagctct[C/T]attattttgagatac | 55130 |
| rs4749269 | snp | C/G | 0.498813 | 0.0243321 | intron-variant | ARMC4 | GRCh38.p7 | 10:27847237 | atcccagtgatgaag[C/G]ccacttgatcatagt | 55130 |
| rs4749272 | snp | C/T | 0.49703 | 0.0384237 | intron-variant | ARMC4 | GRCh38.p7 | 10:27875304 | tgatggtttaaactt[C/T]ctcctttagcttgga | 55130 |
| rs4749273 | snp | C/T | 0.484491 | 0.0866827 | intron-variant | ARMC4 | GRCh38.p7 | 10:27890124 | GTGCAATGAGGGAAC[C/T]GAAGATAGCAAAAGG | 55130 |
| rs4749274 | snp | A/G | 0.493477 | 0.0567349 | intron-variant | ARMC4 | GRCh38.p7 | 10:27896189 | TCTGATATTATACAC[A/G]TCAATGAAATTTTGT | 55130 |
| rs4749275 | snp | A/G | 0.462472 | 0.13174 | intron-variant | ARMC4 | GRCh38.p7 | 10:27896434 | AATATTCAAATTCAA[A/G]TACatagattgatag | 55130 |
| rs4749276 | snp | C/T | 0.462472 | 0.13174 | intron-variant | ARMC4 | GRCh38.p7 | 10:27896667 | ACTCAGAGCAATGTG[C/T]TTATAGGATTAAGGA | 55130 |
| rs4749277 | snp | A/G | 0.462472 | 0.13174 | intron-variant | ARMC4 | GRCh38.p7 | 10:27896683 | TTATAGGATTAAGGA[A/G]CAGTGAGAGCCAGGC | 55130 |
| rs4749278 | snp | C/T | 0.463343 | 0.130326 | intron-variant | ARMC4 | GRCh38.p7 | 10:27899100 | TTTCTGCATTTCCAA[C/T]TGAGGTACCCATCTC | 55130 |
| rs4749279 | snp | A/G | 0.463126 | 0.13068 | intron-variant | ARMC4 | GRCh38.p7 | 10:27899181 | GAAGCAGACTGGGGC[A/G]TCACCTCACTTGGGA | 55130 |
| rs4749280 | snp | A/G | 0.463126 | 0.13068 | intron-variant | ARMC4 | GRCh38.p7 | 10:27899207 | tgggaagcacaaggg[A/G]tcagtgaaatccctc | 55130 |
| rs4749285 | snp | C/T | 0.485664 | 0.0834419 | intron-variant | ARMC4 | GRCh38.p7 | 10:27915436 | GGCAAAGGAGCTCTC[C/T]GGGGACTCTTTTAAA | 55130 |
| rs4749286 | snp | A/G | 0.493523 | 0.0565391 | intron-variant | ARMC4 | GRCh38.p7 | 10:27965558 | AGACAGGACTCATTC[A/G]AGTTTGCATTTAGAG | 55130 |
| rs4749287 | snp | A/T | 0.493477 | 0.0567349 | intron-variant | ARMC4 | GRCh38.p7 | 10:27965607 | GGAACCCAGGAATCC[A/T]GCCTGCCACCCCCTG | 55130 |
| rs4749288 | snp | C/T | 0.49889 | 0.0235361 | intron-variant | ARMC4 | GRCh38.p7 | 10:27966906 | ggtgactctgaaagg[C/T]agagaaaaagaagag | 55130 |
| rs4749289 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27970134 | AATAAATAAATAAAT[A/G]AATAAATAAATAAAT | 55130 |
| rs4749290 | snp | C/T | 0.274929 | 0.248754 | intron-variant | ARMC4 | GRCh38.p7 | 10:27970213 | ATTTTTGCTTTGACG[C/T]CTGTTTATAGAAGGT | 55130 |
| rs4749291 | snp | C/T | 0.257176 | 0.249897 | intron-variant | ARMC4 | GRCh38.p7 | 10:27977887 | catatcagttaatga[C/T]gagtatgtggaagaa | 55130 |
| rs5784030 | in-del | -/AAGGAAA | 0.49706 | 0.0382258 | intron-variant | ARMC4 | GRCh38.p7 | 10:27845135 | ACCAAAGTTGAAATG[-/AAGGAAA]AAGGAAAAAATGTTA | 55130 |
| rs5784031 | snp | A/G | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27869541 | TCTCAAAAAAAAAAA[A/G]GAAAAAGAAAAAAGA | 55130 |
| rs5784032 | in-del | -/A | 0.491157 | 0.065903 | intron-variant | ARMC4 | GRCh38.p7 | 10:27894730 | TAAAAAAAAAAAAAA[-/A]TTGTTGTAGAGGAGT | 55130 |
| rs5784033 | in-del | -/G | 0.494143 | 0.0537956 | intron-variant | ARMC4 | GRCh38.p7 | 10:27951429 | TAATGCAAAGAGAAA[-/G]ATCCAGAAACAAACT | 55130 |
| rs5784034 | in-del | -/C | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27963810 | AGTGAGTTTTTTAGA[-/C]CCCCCATGCATTTGG | 55130 |
| rs5784035 | in-del | -/TT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27988338 | AACACCTGATCTAGC[-/TT]TTTTTTTTTTTTTTT | 55130 |
| rs6481482 | snp | C/G | 0.399611 | 0.200291 | intron-variant | ARMC4 | GRCh38.p7 | 10:27814482 | tcagttccttggcct[C/G]ccattgtcactgatc | 55130 |
| rs6481483 | snp | C/T | 0.390277 | 0.206936 | intron-variant | ARMC4 | GRCh38.p7 | 10:27818485 | ATAATTATTACTTTA[C/T]GAATTTTGTTATTAC | 55130 |
| rs6481484 | snp | A/C | 0.436692 | 0.166271 | intron-variant | ARMC4 | GRCh38.p7 | 10:27834142 | GCCAAGACAAGTCCT[A/C]TGAATGCATTGATTT | 55130 |
| rs6481485 | snp | C/T | 0.441841 | 0.160303 | intron-variant | ARMC4 | GRCh38.p7 | 10:27834435 | CATCATTTCTCACTT[C/T]CCATTGGTGATAACC | 55130 |
| rs6481486 | snp | C/T | 0.483563 | 0.0891524 | intron-variant | ARMC4 | GRCh38.p7 | 10:27843682 | CTGAGGCAGAAGAAT[C/T]GCTTGAACCTGGGAG | 55130 |
| rs6481490 | snp | C/G | 0.482083 | 0.0929373 | intron-variant | ARMC4 | GRCh38.p7 | 10:27908512 | CAGCGGAGAAGAAGG[C/G]CAAACAAAACTTAAT | 55130 |
| rs6481491 | snp | A/G | 0.492533 | 0.0606443 | intron-variant | ARMC4 | GRCh38.p7 | 10:27908714 | TCCTTGAAAATTGAC[A/G]TAAAAACATCTAGAT | 55130 |
| rs6481492 | snp | C/T | 0.333491 | 0.235646 | intron-variant | ARMC4 | GRCh38.p7 | 10:27918464 | atctgatcatctcaa[C/T]agataaaaagcatcg | 55130 |
| rs6481493 | snp | C/T | 0.32885 | 0.23724 | intron-variant | ARMC4 | GRCh38.p7 | 10:27919333 | ACCTTAAAGGACAAC[C/T]GAAAAATTGACCTTC | 55130 |
| rs6481494 | snp | C/T | 0.33303 | 0.235809 | intron-variant | ARMC4 | GRCh38.p7 | 10:27927238 | ATGAATTCTACTCCA[C/T]AAAGTTAATAAAACT | 55130 |
| rs6481495 | snp | G/T | 0.139564 | 0.224285 | intron-variant | ARMC4 | GRCh38.p7 | 10:27946165 | tattctacattatgt[G/T]tatatataaatttaa | 55130 |
| rs6481496 | snp | A/C | 0.280785 | 0.248097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27946224 | AAATATAAAAAATAC[A/C]AATATAAAAATGTAT | 55130 |
| rs6481497 | snp | G/T | 0.499354 | 0.0179596 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27998082 | ATGAAACCCATTCGG[G/T]AATCACATCGTTAAC | 55130 |
| rs7068054 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | ARMC4 | GRCh38.p7 | 10:27969881 | gaggcagaagtgggc[A/G]gattacttgagctca | 55130 |
| rs7070860 | snp | C/G | 0.462472 | 0.13174 | intron-variant | ARMC4 | GRCh38.p7 | 10:27894987 | AGAAAATTAGACAGG[C/G]ATATGGAAAGACATA | 55130 |
| rs7071498 | snp | C/G | 0.0869089 | 0.189476 | intron-variant | ARMC4 | GRCh38.p7 | 10:27953168 | ttcttgtggtaagaa[C/G]acttaatctgagatt | 55130 |
| rs7071570 | snp | C/T | 0.291493 | 0.246533 | intron-variant | ARMC4 | GRCh38.p7 | 10:27925559 | gacagggcctcatta[C/T]gttttccaggctggt | 55130 |
| rs7071799 | snp | A/G | 0.0876345 | 0.190099 | intron-variant | ARMC4 | GRCh38.p7 | 10:27830516 | ATTTTAGAGAAGAGA[A/G]TTTTTCAGCCAAATC | 55130 |
| rs7072445 | snp | A/C | 0.0640965 | 0.167152 | intron-variant | ARMC4 | GRCh38.p7 | 10:27883018 | atcttagaagtgaga[A/C]gtgtgtacagagatt | 55130 |
| rs7072798 | snp | C/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27971011 | AAATAAATAAATAAA[C/T]AAACAAACAAAATAA | 55130 |
| rs7072799 | snp | C/T | 0.314787 | 0.241459 | intron-variant | ARMC4 | GRCh38.p7 | 10:27971015 | AAATAAATAAACAAA[C/T]AAACAAAATAAAATA | 55130 |
| rs7073702 | snp | C/T | 0.33303 | 0.235809 | intron-variant | ARMC4 | GRCh38.p7 | 10:27927599 | ACAGGTACAAAAGGA[C/T]TCACTAACCTCCTTG | 55130 |
| rs7074114 | snp | A/T | 0.0970103 | 0.197722 | intron-variant | ARMC4 | GRCh38.p7 | 10:27837594 | AAACTGAATGATGGT[A/T]TTCACTGCTGTAAAT | 55130 |
| rs7074562 | snp | C/T | 0.494187 | 0.0535994 | intron-variant | ARMC4 | GRCh38.p7 | 10:27949907 | AAAGGATGCTACAAG[C/T]GTAGATGAAACTCCA | 55130 |
| rs7076149 | snp | A/G | 0.34659 | 0.230587 | intron-variant | ARMC4 | GRCh38.p7 | 10:27858907 | CTCCCAGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 55130 |
| rs7076362 | snp | A/G | 0.030665 | 0.119967 | intron-variant | ARMC4 | GRCh38.p7 | 10:27919489 | acaatccaattaaaa[A/G]tgggcaaaagacttt | 55130 |
| rs7077304 | snp | A/G | 0.490508 | 0.0682328 | intron-variant | ARMC4 | GRCh38.p7 | 10:27876786 | CACACTTTCCAGTAC[A/G]CTTACTGTGTTACAA | 55130 |
| rs7077472 | snp | A/G | 0.465158 | 0.127307 | intron-variant | ARMC4 | GRCh38.p7 | 10:27907034 | aaaaaTTCAACAGGC[A/G]GAAATAACTTCAGCA | 55130 |
| rs7077784 | snp | C/T | 0.336017 | 0.234736 | intron-variant | ARMC4 | GRCh38.p7 | 10:27819301 | GGAAAGAGAACTTCA[C/T]CCTGTTTTGAAGAGT | 55130 |
| rs7077813 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | ARMC4 | GRCh38.p7 | 10:27906978 | gtaacaaacctgcac[G/T]ttctgcacatgtatc | 55130 |
| rs7077984 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27845159 | ggaaaaaatgttaag[G/T]gcagccagagagaaa | 55130 |
| rs7078174 | snp | G/T | 0.0193772 | 0.0965046 | intron-variant | ARMC4 | GRCh38.p7 | 10:27819390 | ACTATGAAAGATTAA[G/T]GACTTAAAGCTTAAT | 55130 |
| rs7078534 | snp | A/T | 0.441841 | 0.160303 | intron-variant | ARMC4 | GRCh38.p7 | 10:27834787 | CCTAGTGATTCTCTC[A/T]TTTAATTCTCAGATG | 55130 |
| rs7079452 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | ARMC4 | GRCh38.p7 | 10:27814250 | acccaggaagaggag[A/G]ggtcaggctcctgcc | 55130 |
| rs7081199 | snp | C/T | 0.0655868 | 0.168795 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999083 | TGCGCCCGCGCTGGG[C/T]TCCACCCGCCCCGGC | 55130 |
| rs7081236 | snp | A/C | 0.318896 | 0.240319 | intron-variant | ARMC4 | GRCh38.p7 | 10:27985433 | TTTGTATTGTAACAT[A/C]ATCTATATATCTCCC | 55130 |
| rs7081305 | snp | C/T | 0.499722 | 0.0117779 | intron-variant | ARMC4 | GRCh38.p7 | 10:27823476 | TAACTGTATGTGACC[C/T]GAGGTAACTCTCTCT | 55130 |
| rs7083832 | snp | C/T | 0.100944 | 0.200705 | intron-variant | ARMC4 | GRCh38.p7 | 10:27902992 | ctggcagagacacaa[C/T]aaaaaaaagaaaatg | 55130 |
| rs7084678 | snp | C/G | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27933735 | ATGAATAGCAAAGTG[C/G]GTTTCAAAAACATAA | 55130 |
| rs7085331 | snp | C/T | 0.448452 | 0.152042 | intron-variant | ARMC4 | GRCh38.p7 | 10:27833050 | AAGAGATTGGCTTTC[C/T]CCCTTGCCTGGCCGT | 55130 |
| rs7085555 | snp | A/G | 0.449345 | 0.150869 | intron-variant | ARMC4 | GRCh38.p7 | 10:27833064 | CCCCCTTGCCTGGCC[A/G]TGCTTTTTGAAGTTT | 55130 |
| rs7087095 | snp | A/C | 0.485799 | 0.0830599 | intron-variant | ARMC4 | GRCh38.p7 | 10:27943930 | TATCTCTTACCTCCC[A/C]TGCATGTATACTTGG | 55130 |
| rs7089040 | snp | A/C | 0.485664 | 0.0834419 | intron-variant | ARMC4 | GRCh38.p7 | 10:27962023 | GTAAACCTTTATTAC[A/C]TCATCACACCACTGC | 55130 |
| rs7090390 | snp | C/T | 0.461592 | 0.133149 | intron-variant | ARMC4 | GRCh38.p7 | 10:27891967 | AATTTAATATATGGA[C/T]TTTTACCAGATTCAG | 55130 |
| rs7090545 | snp | A/G/T | | | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:28000905 | ATTTATCATGACTTG[A/G/T]TTTTTTtttttcttt | 55130 |
| rs7091489 | snp | C/G | 0.138886 | 0.22395 | intron-variant | ARMC4 | GRCh38.p7 | 10:27950498 | CTTAAATAAATCAGA[C/G]TCAGGTTGTTGTATT | 55130 |
| rs7092221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27937773 | TGCCATGTTTATCTT[C/T]TGCACGTGATTTTCA | 55130 |
| rs7092735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27998195 | TAACATCCACGGGGA[A/G]TCCGCGCATACACTG | 55130 |
| rs7093199 | snp | A/T | 0.484209 | 0.0874434 | intron-variant | ARMC4 | GRCh38.p7 | 10:27850742 | taaaaatggaaaaaa[A/T]ctgtgaaacaacaac | 55130 |
| rs7093744 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | ARMC4 | GRCh38.p7 | 10:27985926 | AACCAATATGGTTGA[A/G]AATGAAGGAGAAAGT | 55130 |
| rs7093804 | snp | A/G | 0.0667028 | 0.170006 | intron-variant | ARMC4 | GRCh38.p7 | 10:27928223 | GTAAGTGGTACCAAT[A/G]TCCATATAGTTACCC | 55130 |
| rs7093861 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ARMC4 | GRCh38.p7 | 10:27935420 | gagctgacgtctaac[C/T]cagccatctgctcca | 55130 |
| rs7094089 | snp | A/T | 0.397994 | 0.201489 | intron-variant | ARMC4 | GRCh38.p7 | 10:27898336 | CAATTTCCAAAAAAA[A/T]CAGTTTTAAGCCTAT | 55130 |
| rs7094167 | snp | C/T | 0.463126 | 0.13068 | intron-variant | ARMC4 | GRCh38.p7 | 10:27898286 | CTTAGTATTCATCCT[C/T]TCTACTAAATTTGTG | 55130 |
| rs7094492 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27928729 | ATACTATGCAATCTG[A/C]CTTTCATTTTCTAGT | 55130 |
| rs7094524 | snp | C/T | 0.33693 | 0.2344 | intron-variant | ARMC4 | GRCh38.p7 | 10:27919533 | acaatatatacaaat[C/T]ggtaataaagatatg | 55130 |
| rs7094542 | snp | A/G | 0.463343 | 0.130326 | intron-variant | ARMC4 | GRCh38.p7 | 10:27898395 | CTTAGGTGTTTCTGA[A/G]AATATTAATTTTAAA | 55130 |
| rs7094669 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | ARMC4 | GRCh38.p7 | 10:27898446 | ATCTCTGTTTCTTCT[G/T]AAGTCAGTTCTGCTA | 55130 |
| rs7094709 | snp | C/T | 0.089084 | 0.191327 | intron-variant | ARMC4 | GRCh38.p7 | 10:27947261 | AAGCCAGTACTTCCA[C/T]TTCCTCTTTTAAAAA | 55130 |
| rs7095239 | snp | C/T | 0.465052 | 0.127485 | intron-variant | ARMC4 | GRCh38.p7 | 10:27906791 | caccgcatgttctca[C/T]tcataagcgggagtt | 55130 |
| rs7095395 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ARMC4 | GRCh38.p7 | 10:27906911 | gagaaatacctaatg[C/T]agatgacgggttgat | 55130 |
| rs7095692 | snp | C/T | 0.465158 | 0.127307 | intron-variant | ARMC4 | GRCh38.p7 | 10:27907082 | CAATCTCTAAACCTA[C/T]AGAAAAAATGTTAAG | 55130 |
| rs7096753 | snp | A/G | 0.0535932 | 0.154675 | intron-variant | ARMC4 | GRCh38.p7 | 10:27856639 | tctggcaaggaaacc[A/G]ctagccactagtgag | 55130 |
| rs7096964 | snp | C/G | 0.442385 | 0.15965 | intron-variant | ARMC4 | GRCh38.p7 | 10:27880915 | gggtgggaatggaag[C/G]cagcatcataaagat | 55130 |
| rs7097367 | snp | G/T | 0.388775 | 0.207946 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999128 | CGCTCGGCCCCTCCC[G/T]GGAAACACTTTTATT | 55130 |
| rs7097374 | snp | C/T | 0.0670745 | 0.170406 | intron-variant | ARMC4 | GRCh38.p7 | 10:27932392 | cgtatttttgcacca[C/T]caaatattaaaaatt | 55130 |
| rs7097725 | snp | A/C | 0.375 | 0.216506 | intron-variant | ARMC4 | GRCh38.p7 | 10:27969516 | TCACTTGCCAGTTAA[A/C]AAAGTTGCCCATGCA | 55130 |
| rs7097726 | snp | A/G | 0.375 | 0.216506 | intron-variant | ARMC4 | GRCh38.p7 | 10:27969518 | ACTTGCCAGTTAAAA[A/G]AGTTGCCCATGCATT | 55130 |
| rs7097949 | snp | A/G | 0.0399833 | 0.135621 | intron-variant | ARMC4 | GRCh38.p7 | 10:27928840 | tattatatgtcagtc[A/G]ctttacttacataaa | 55130 |
| rs7099233 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27964596 | GTGGTTTTGTTTTTG[A/G]AGATTTGATCTGTTT | 55130 |
| rs7099583 | snp | A/G | 0.462144 | 0.132269 | intron-variant | ARMC4 | GRCh38.p7 | 10:27893882 | AGGCCAGGTGTGGTG[A/G]CTCAGGCCTGTAATC | 55130 |
| rs7099871 | snp | A/C | 0.462034 | 0.132445 | intron-variant | ARMC4 | GRCh38.p7 | 10:27894133 | GGCCAAGAGTGAGAC[A/C]CCATCTCTAAAAAAT | 55130 |
| rs7099876 | snp | A/G | 0.462034 | 0.132445 | intron-variant | ARMC4 | GRCh38.p7 | 10:27894136 | CAAGAGTGAGACACC[A/G]TCTCTAAAAAATAAA | 55130 |
| rs7100494 | snp | A/G | 0.462144 | 0.132269 | intron-variant | ARMC4 | GRCh38.p7 | 10:27894277 | ATATAACCAAGTGGG[A/G]AAAGTTTTGGATAGT | 55130 |
| rs7100534 | snp | A/G | 0.0785177 | 0.181917 | intron-variant | ARMC4 | GRCh38.p7 | 10:27829548 | TCAAATGTGGTTGTT[A/G]TTTCTTTTTTATAAC | 55130 |
| rs7100957 | snp | C/T | 0.093777 | 0.195178 | intron-variant | ARMC4 | GRCh38.p7 | 10:27878397 | CTGGGTGTTTTGGCG[C/T]AAAGCAATTAAATTA | 55130 |
| rs7358162 | snp | A/G | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27890856 | ATGGGTGCATACTTA[A/G]AACTATTTGGTGACT | 55130 |
| rs7358164 | snp | A/C | 0.0644693 | 0.167566 | intron-variant | ARMC4 | GRCh38.p7 | 10:27891093 | CAAAGTTCTCATTGG[A/C]TCCCTGATTGGGCAT | 55130 |
| rs7475103 | snp | C/T | 0.484066 | 0.0878235 | intron-variant | ARMC4 | GRCh38.p7 | 10:27849509 | cacataggtaaaaaa[C/T]ctgcacattgtgcac | 55130 |
| rs7476055 | snp | C/T | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27842614 | GTCTTTAAGAACATT[C/T]TATAAAGCCATGGGC | 55130 |
| rs7476072 | snp | C/T | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27842683 | TCCCCACAGtaaaat[C/T]tttaaatttaaatat | 55130 |
| rs7476534 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27863779 | TTCTGGTTGGACAAA[C/T]CATCATGTTGCACAG | 55130 |
| rs7478433 | snp | A/T | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27863778 | ATTCTGGTTGGACAA[A/T]TCATCATGTTGCACA | 55130 |
| rs7893159 | snp | A/G | 0.0966517 | 0.197444 | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27857592 | tgtgacatttctgct[A/G]ggcagcgctgCTTTA | 55130 |
| rs7893462 | snp | A/G | 0.497357 | 0.0362559 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27939936 | CTCCTGCAGCTGCTC[A/G]TTCTCACTATTTAGG | 55130 |
| rs7893558 | snp | C/T | 0.0744748 | 0.178019 | intron-variant | ARMC4 | GRCh38.p7 | 10:27969966 | CAAAAATTAGCCAGC[C/T]GTGGTGTCACACACC | 55130 |
| rs7894399 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | ARMC4 | GRCh38.p7 | 10:27843586 | ggctgaccaacatga[C/T]gaaacaccacctata | 55130 |
| rs7895005 | snp | A/C/G | 0.0193772 | 0.0965046 | utr-variant-3-prime, intron-variant | ARMC4 | GRCh38.p7 | 10:27812435 | AACAACTGTTTCCCA[A/C/G]TTTAGGCTTTCTGGC | 55130 |
| rs7895017 | snp | A/G | 0.0829062 | 0.185956 | intron-variant | ARMC4 | GRCh38.p7 | 10:27900037 | gacacctcccagcag[A/G]ggtggacagacacct | 55130 |
| rs7896104 | snp | C/T | 0.496999 | 0.0386216 | intron-variant | ARMC4 | GRCh38.p7 | 10:27887825 | ATAAAAAAATTCAGA[C/T]TTTAAATTAGATTTT | 55130 |
| rs7896548 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ARMC4 | GRCh38.p7 | 10:27953098 | gtgcaatcattacta[C/T]gatgaaagtaataaa | 55130 |
| rs7896625 | snp | A/G | 0.329783 | 0.236927 | intron-variant | ARMC4 | GRCh38.p7 | 10:27952969 | TAGTGTGCATATATT[A/G]TTTTTCTCTTTGTTT | 55130 |
| rs7896951 | snp | A/G | 0.499575 | 0.0145705 | intron-variant | ARMC4 | GRCh38.p7 | 10:27953488 | CCAAACAATGTGTAA[A/G]AATATTAGCTGCAGT | 55130 |
| rs7897553 | snp | C/T | 0.485187 | 0.0847778 | intron-variant | ARMC4 | GRCh38.p7 | 10:27913037 | AAAGCAGGAGGATAG[C/T]CTATGCTTTCATAGT | 55130 |
| rs7897889 | snp | A/C | 0.465052 | 0.127485 | intron-variant | ARMC4 | GRCh38.p7 | 10:27906114 | tttttgcaatctatc[A/C]atctgacaaagggct | 55130 |
| rs7897948 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | ARMC4 | GRCh38.p7 | 10:27992041 | GTGGCTATGGGTTAC[A/T]GAACTTTCTTTGGTT | 55130 |
| rs7898085 | snp | A/G | 0.454212 | 0.144213 | intron-variant, synonymous-codon | ARMC4 | GRCh38.p7 | 10:27853316 | aggttgcagtgagcc[A/G]agatcgttgtcactg | 55130 |
| rs7900709 | snp | A/C | 0.0588605 | 0.161139 | intron-variant | ARMC4 | GRCh38.p7 | 10:27918957 | tatcaatcacaaaac[A/C]acaaataagtagata | 55130 |
| rs7900724 | snp | A/C | 0.490119 | 0.0695896 | intron-variant | ARMC4 | GRCh38.p7 | 10:27858870 | GTGCAGTGGTGTGAT[A/C]TCAGCTCACTGCAAC | 55130 |
| rs7901785 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | ARMC4 | GRCh38.p7 | 10:27934767 | ATAAAGGTTTCCACA[C/T]GGGAAATTGATTACC | 55130 |
| rs7902721 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27875345 | cttctgaagccttct[C/T]ctctcaactcatcaa | 55130 |
| rs7902862 | snp | A/T | 0.0298908 | 0.118541 | intron-variant | ARMC4 | GRCh38.p7 | 10:27868189 | gaaacaacatgcttg[A/T]gagtctgtggagaaa | 55130 |
| rs7903751 | snp | A/G | 0.081446 | 0.184634 | intron-variant | ARMC4 | GRCh38.p7 | 10:27989773 | GGATCACTTGAGCCC[A/G]GGAGGCGGGAGGATG | 55130 |
| rs7907231 | snp | C/T | 0.332337 | 0.236052 | intron-variant | ARMC4 | GRCh38.p7 | 10:27915607 | TGGGGAATTATgata[C/T]gattaaattctgact | 55130 |
| rs7907415 | snp | G/T | 0.494143 | 0.0537956 | intron-variant | ARMC4 | GRCh38.p7 | 10:27957076 | CCATCTCCTTTAATC[G/T]CTGGAAGTGATCAAA | 55130 |
| rs7907500 | snp | C/G | 0.493658 | 0.0559517 | intron-variant | ARMC4 | GRCh38.p7 | 10:27908360 | TTATAATTACTTAAA[C/G]ACACTGTAATCAAAA | 55130 |
| rs7907935 | snp | C/T | 0.4941 | 0.0539917 | intron-variant | ARMC4 | GRCh38.p7 | 10:27957480 | GTAAGACAGACAACC[C/T]GAACCATCAGGATAG | 55130 |
| rs7908625 | snp | A/G | 0.021333 | 0.101051 | intron-variant | ARMC4 | GRCh38.p7 | 10:27836053 | agcctgaagaggagg[A/G]agaggaagaggggtt | 55130 |
| rs7908626 | snp | A/G | 0.436834 | 0.166111 | intron-variant | ARMC4 | GRCh38.p7 | 10:27836054 | gcctgaagaggagga[A/G]gaggaagaggggttg | 55130 |
| rs7908757 | snp | A/G | 0.331179 | 0.236453 | intron-variant | ARMC4 | GRCh38.p7 | 10:27933692 | GAAATACATGCAGCC[A/G]TTTCTGGCAAGTGTT | 55130 |
| rs7908864 | snp | A/T | 0.0486741 | 0.148216 | intron-variant | ARMC4 | GRCh38.p7 | 10:27843458 | TCCTGATTACCTGAG[A/T]GGTAACTGTAAAACT | 55130 |
| rs7913482 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ARMC4 | GRCh38.p7 | 10:27934668 | AGAAGGCTACTATGA[A/G]AATGTACCTGACACT | 55130 |
| rs7915784 | snp | A/G | 0.27893 | 0.24832 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997811 | TGCTCCCCGGTTTCT[A/G]CCCATTGCCAAGCTC | 55130 |
| rs7915894 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | ARMC4 | GRCh38.p7 | 10:27945098 | TGAATCAGGTAGAGC[C/G]GAAGCATGGAAAAGC | 55130 |
| rs7916427 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ARMC4 | GRCh38.p7 | 10:27880505 | ttgaatgtttatgtc[C/T]cctcaaaattcatgt | 55130 |
| rs7916958 | snp | C/T | 0.495291 | 0.0482933 | intron-variant | ARMC4 | GRCh38.p7 | 10:27938604 | TGTCTCttctttttt[C/T]ttttttttttctctt | 55130 |
| rs7917840 | snp | A/T | 0.499846 | 0.00878459 | intron-variant | ARMC4 | GRCh38.p7 | 10:27993574 | agaattgcttgaacc[A/T]gagaggtggaacttg | 55130 |
| rs7917842 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | ARMC4 | GRCh38.p7 | 10:27859184 | AGACAATGGCCTTTT[C/T]AGCATTCCTGAACAA | 55130 |
| rs7918234 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | ARMC4 | GRCh38.p7 | 10:27875710 | gctgcaggacagtgg[A/G]tgcagcccaccgagc | 55130 |
| rs7920186 | snp | C/T | 0.305389 | 0.243787 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27968923 | TGACCAGAAACATAC[C/T]GAAGTAATTGTGCTC | 55130 |
| rs7921228 | snp | C/G | 0.475702 | 0.107512 | intron-variant | ARMC4 | GRCh38.p7 | 10:27939621 | TAAACACCTGAAGTG[C/G]CGGCTACTTGGGAGG | 55130 |
| rs7921313 | snp | A/G | 0.101301 | 0.200969 | intron-variant | ARMC4 | GRCh38.p7 | 10:27969574 | AACAGAGCCACAAAA[A/G]TCAAACACCCCAAAA | 55130 |
| rs7921344 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27993974 | AATATATATATATAT[A/G]TGTGTGTGTGTGTGT | 55130 |
| rs7922435 | snp | C/T | 0.330249 | 0.23677 | intron-variant | ARMC4 | GRCh38.p7 | 10:27957415 | TAGCAAGATGCCCTG[C/T]GAGATACAGCAATAA | 55130 |
| rs7923373 | snp | A/G | 0.0744748 | 0.178019 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27982288 | ACCAGTGTGTTTTAA[A/G]CTTTGTTGTAATTAT | 55130 |
| rs7924172 | snp | C/T | 0.48546 | 0.0840147 | intron-variant | ARMC4 | GRCh38.p7 | 10:27952728 | GGGCATAAGGGTCTT[C/T]TGTTTATTTGCTCCA | 55130 |
| rs9299592 | in-del | -/T/TT | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27858821 | TTTTTTTTTTTTTTT[-/T/TT]GAGACAGAGTCTCGC | 55130 |
| rs9299593 | snp | A/T | 0.0185938 | 0.0946107 | intron-variant | ARMC4 | GRCh38.p7 | 10:27921836 | ATAGAGCAGTATTTT[A/T]TTTTTTTTTTTGTAA | 55130 |
| rs9299594 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | ARMC4 | GRCh38.p7 | 10:27947917 | GTTTTCTTTGGTAGC[A/G]ATTTTCGAGCTTATA | 55130 |
| rs9299595 | snp | A/G | 0.140919 | 0.224948 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997738 | TAAATAAATAAATAA[A/G]TGGTGTTCAAAAATG | 55130 |
| rs9334541 | snp | C/T | 0.0769736 | 0.180449 | intron-variant | ARMC4 | GRCh38.p7 | 10:27981683 | TATTATTTTCATCTC[C/T]GAAGGATCTATATGG | 55130 |
| rs9416762 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | ARMC4 | GRCh38.p7 | 10:27911100 | aggaacatcgccgcc[A/G]tcctgcacttaggaa | 55130 |
| rs9416763 | snp | A/G | 0.489024 | 0.0732638 | intron-variant | ARMC4 | GRCh38.p7 | 10:27988971 | GACAGAGGCAGCGAC[A/G]GGGATATGCTGATGG | 55130 |
| rs9417567 | snp | C/T | 0.101301 | 0.200969 | intron-variant | ARMC4 | GRCh38.p7 | 10:27923936 | gtgatagagagagac[C/T]ctgtctaatgaaaga | 55130 |
| rs9663255 | snp | A/G | 0.462472 | 0.13174 | intron-variant | ARMC4 | GRCh38.p7 | 10:27905590 | AAGAACAAGGCTGGA[A/G]GCATCACACTACCTG | 55130 |
| rs9671379 | snp | A/G | 0.459184 | 0.136902 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872947 | TACCAGCTCCTCCTT[A/G]TACCTCTGGTAGAAT | 55130 |
| rs9671844 | snp | A/C | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872757 | GCTGGATTCGGTTTG[A/C]CAGTATTTTATTGAG | 55130 |
| rs9733579 | snp | A/C | 0.0966517 | 0.197444 | intron-variant | ARMC4 | GRCh38.p7 | 10:27847206 | tgaatccagcagcaa[A/C]tcaaaaagcttatcc | 55130 |
| rs9733581 | snp | C/T | 0.081446 | 0.184634 | intron-variant | ARMC4 | GRCh38.p7 | 10:27847272 | ggcttgttcaacata[C/T]gcaaatcaataaacg | 55130 |
| rs9769304 | snp | A/G | 0.442113 | 0.159977 | intron-variant | ARMC4 | GRCh38.p7 | 10:27846010 | CTTTCTGTCTCATTG[A/G]TCTGTCTAATGTTGA | 55130 |
| rs9971114 | snp | C/T | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27852843 | gcatgagcctgtaat[C/T]tcagctactcaggag | 55130 |
| rs10047834 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27872742 | gctttttgatgtgct[A/G]ctggattcggtttgt | 55130 |
| rs10218312 | snp | A/G | 0.444444 | 0.157135 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872903 | ATTCCCTCTTTTTCT[A/G]TTGATTGGAACAGTT | 55130 |
| rs10256670 | snp | C/T | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872589 | gaattttgtcaaagg[C/T]cttttctgcatctgt | 55130 |
| rs10466056 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27924612 | gctaaattgattagg[A/G]ggaaaaaaaaaaaaa | 55130 |
| rs10508726 | snp | A/G | 0.495407 | 0.0477027 | intron-variant | ARMC4 | GRCh38.p7 | 10:27839667 | CTTTATGTTTAAACC[A/G]CAGCGTTTTTCTGGC | 55130 |
| rs10569745 | in-del | -/A | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27890772 | GGTATATATATATTT[-/A]AAAAAAAAAAAAACT | 55130 |
| rs10580710 | in-del | -/TATATATA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27827380 | TACACACACACACAC[-/TATATATA]TATATATATATATAT | 55130 |
| rs10588409 | in-del | -/A | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27890785 | TTAAAAAAAAAAAAA[-/A]CTTGTATTATCATTC | 55130 |
| rs10597575 | in-del | -/ATGA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27954527 | TGAATGAATGAATGA[-/ATGA]GTTGAAGCTTAAGGG | 55130 |
| rs10599433 | in-del | -/A | 0.122134 | 0.214826 | intron-variant | ARMC4 | GRCh38.p7 | 10:27985217 | TCTCTGTTAGCTGCC[-/A]AAAAAAAAAAAAAGG | 55130 |
| rs10658728 | in-del | -/CA/TA/TATA | 0.140919 | 0.224948 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940257 | ATATATAAATGTCAG[-/CA/TA/TATA]TATATGTGATATATA | 55130 |
| rs10658729 | in-del | -/TG | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940265 | ATGTCAGTATATGTG[-/TG]ATATATATATAAATG | 55130 |
| rs10677175 | in-del | -/TT | 0.578727 | 0.106884 | intron-variant | ARMC4 | GRCh38.p7 | 10:27859056 | GTTTCTTTTTTTTTT[-/TT]AAGACTGCATACTTA | 55130 |
| rs10684689 | in-del | -/TA | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27946022 | GTGTATATATATATA[-/TA]ATTATGTATACAAAT | 55130 |
| rs10708986 | in-del | -/A | 0.49681 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27941324 | TCCTGTTTCCACTGG[-/A]AAAAAAAAAAAAAAG | 55130 |
| rs10713871 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27850466 | AAAAAAAAAAAAAAA[-/A]GAATCACTTGAACGT | 55130 |
| rs10763622 | snp | A/C | 0.391954 | 0.205789 | intron-variant | ARMC4 | GRCh38.p7 | 10:27813746 | TATTTAAGCACTTTA[A/C]TCAGGGGAATGACAT | 55130 |
| rs10763623 | snp | A/T | 0.0209421 | 0.100162 | intron-variant | ARMC4 | GRCh38.p7 | 10:27819794 | TCTAGGAAGGAGTGA[A/T]CAGCACAATGCATCT | 55130 |
| rs10763626 | snp | C/T | 0.437683 | 0.165152 | intron-variant | ARMC4 | GRCh38.p7 | 10:27845728 | AGGTATGGAGGAAGA[C/T]CTACCAAGCAAATGG | 55130 |
| rs10763627 | snp | A/G | 0.496905 | 0.0392151 | intron-variant | ARMC4 | GRCh38.p7 | 10:27845762 | ACAAAAAAAGGCAGG[A/G]GTTGCAATCCTAGTC | 55130 |
| rs10763628 | snp | C/T | 0.49975 | 0.0111793 | intron-variant | ARMC4 | GRCh38.p7 | 10:27852725 | CAGCACTTTGGGAGG[C/T]GGAGGCGGGTGGATC | 55130 |
| rs10763629 | snp | C/T | 0.499776 | 0.0105807 | intron-variant | ARMC4 | GRCh38.p7 | 10:27854875 | GAATGTGAATTAATA[C/T]GAAAATAAGTAAGCT | 55130 |
| rs10826352 | snp | C/T | 0.496842 | 0.0396107 | intron-variant | ARMC4 | GRCh38.p7 | 10:27844079 | GACATGCACCTGCAG[C/T]CCCAGCTACTGGGGA | 55130 |
| rs10826354 | snp | A/G | 0.192088 | 0.2432 | intron-variant | ARMC4 | GRCh38.p7 | 10:27852516 | CTAAAGCAATCACTA[A/G]ATGACAACACGGAAT | 55130 |
| rs10826355 | snp | G/T | 0.49703 | 0.0384237 | intron-variant | ARMC4 | GRCh38.p7 | 10:27876076 | GTGGAGCCCACTGCA[G/T]CTCAAGGATGCCTGC | 55130 |
| rs10826356 | snp | C/T | 0.49706 | 0.0382258 | intron-variant | ARMC4 | GRCh38.p7 | 10:27883414 | AACAAATACAGGCCA[C/T]GGGAAGGGGAGAGTC | 55130 |
| rs10826357 | snp | A/G | 0.4628 | 0.13121 | intron-variant | ARMC4 | GRCh38.p7 | 10:27892378 | AGACTAAAAAAGACC[A/G]TGCGGCTTTCTAAGT | 55130 |
| rs10826358 | snp | C/T | 0.450609 | 0.149185 | intron-variant | ARMC4 | GRCh38.p7 | 10:27892492 | TTTCCTATCAGATAA[C/T]GAATGGACCGATAAT | 55130 |
| rs10826359 | snp | C/T | 0.464523 | 0.128375 | intron-variant | ARMC4 | GRCh38.p7 | 10:27892509 | AATGGACCGATAATT[C/T]TTAAGCTGGAAAAAC | 55130 |
| rs10826360 | snp | A/G | 0.462034 | 0.132445 | intron-variant | ARMC4 | GRCh38.p7 | 10:27892880 | ACGGCCGGGTGTGGT[A/G]ACTCACGCCTGTAAT | 55130 |
| rs10826362 | snp | C/T | 0.462363 | 0.131916 | intron-variant | ARMC4 | GRCh38.p7 | 10:27900676 | AAGCATACACAAGTA[C/T]CAATAGCTGAATCGA | 55130 |
| rs10826363 | snp | A/G | 0.462582 | 0.131564 | intron-variant | ARMC4 | GRCh38.p7 | 10:27902274 | GAGAACAATGACACA[A/G]CGTACCAGAATCTAT | 55130 |
| rs10826364 | snp | A/T | 0.464841 | 0.127841 | intron-variant | ARMC4 | GRCh38.p7 | 10:27906277 | GCTCATCATCACTGG[A/T]CATTAGAGACATGCA | 55130 |
| rs10826365 | snp | A/G | 0.465052 | 0.127485 | intron-variant | ARMC4 | GRCh38.p7 | 10:27906455 | GAAGACAGTGTGGCG[A/G]TTCCTCAAGGATCTA | 55130 |
| rs10826366 | snp | A/G | 0.00475057 | 0.0485048 | intron-variant | ARMC4 | GRCh38.p7 | 10:27924799 | TCCTAATAAAATGCA[A/G]ATTTCCAAAATTGAG | 55130 |
| rs10826367 | snp | C/G | 0.452965 | 0.145963 | intron-variant | ARMC4 | GRCh38.p7 | 10:27935975 | TAATAAATTTCAGCT[C/G]TATTTAAGTACCATG | 55130 |
| rs10826368 | snp | A/G | 0.277334 | 0.248501 | intron-variant | ARMC4 | GRCh38.p7 | 10:27937896 | GTCAGGGCTATATAC[A/G]ATTGTTATGGGCCAA | 55130 |
| rs10826370 | snp | C/G | 0.485799 | 0.0830599 | intron-variant | ARMC4 | GRCh38.p7 | 10:27942049 | CTGCAGGTGGGATAG[C/G]AACGTGGGAAAAATT | 55130 |
| rs10826373 | snp | C/T | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27948604 | CACGCATTTGCATTT[C/T]TGAGGTTTTAGGAGC | 55130 |
| rs10826374 | snp | C/T | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27948656 | TGATTTTACTAGCTT[C/T]TGAAGGGCTTTGAAA | 55130 |
| rs10826376 | snp | A/C | 0.0379877 | 0.132479 | intron-variant | ARMC4 | GRCh38.p7 | 10:27958407 | GGGAGGATATTATTG[A/C]GGCTGTTCACTCTCT | 55130 |
| rs10826377 | snp | C/T | 0.040671 | 0.13668 | intron-variant | ARMC4 | GRCh38.p7 | 10:27958428 | TTCACTCTCTCACTC[C/T]GTGCCTGCCCCATTA | 55130 |
| rs10826379 | snp | A/G | 0.499693 | 0.0123764 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984646 | TTTGAAAATAACAAG[A/G]CCACCTAATGTCTTC | 55130 |
| rs11006728 | snp | C/T | 0.141258 | 0.225111 | intron-variant | ARMC4 | GRCh38.p7 | 10:27819123 | TTGATCTTTCCCCTT[C/T]CTATTTTGTCTGATG | 55130 |
| rs11006729 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27820715 | CACAAGGCTTCATTC[G/T]ATATCCCATATGCTG | 55130 |
| rs11006730 | snp | A/C | 0.0836354 | 0.186609 | intron-variant | ARMC4 | GRCh38.p7 | 10:27821550 | AAACTAGCAAATACT[A/C]GCACAACAGAAAGTT | 55130 |
| rs11006731 | snp | G/T | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27821965 | AGCCCCCACGCTTTT[G/T]AAAACTTAACTGCAC | 55130 |
| rs11006732 | snp | A/G | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27821966 | GCCCCCACGCTTTTG[A/G]AAACTTAACTGCACA | 55130 |
| rs11006733 | snp | C/T | 0.154661 | 0.231107 | intron-variant | ARMC4 | GRCh38.p7 | 10:27825417 | GAAAAGACAACTTAG[C/T]GATCTGGGAGGATGG | 55130 |
| rs11006734 | snp | C/T | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27826318 | CAGGCTTCCGGATCA[C/T]GTACATCCATTGCAG | 55130 |
| rs11006736 | snp | A/C | 0.434543 | 0.168653 | intron-variant | ARMC4 | GRCh38.p7 | 10:27832208 | TCAGAATCCTTAAAA[A/C]ATATCCTTGAATAAT | 55130 |
| rs11006737 | snp | A/T | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27840215 | TTATTGATCTATTTG[A/T]ACATATTTACGTACA | 55130 |
| rs11006739 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | ARMC4 | GRCh38.p7 | 10:27846729 | AGACGCAATAAAAAA[A/T]GACAAAGGGGATATC | 55130 |
| rs11006741 | snp | C/T | 0.497121 | 0.0378299 | intron-variant | ARMC4 | GRCh38.p7 | 10:27847947 | AAATGGAAGAACATC[C/T]CATGCTCTTGGATAG | 55130 |
| rs11006742 | snp | C/T | 0.497121 | 0.0378299 | intron-variant | ARMC4 | GRCh38.p7 | 10:27849223 | AGTACTATGCAGCCA[C/T]GAAAAAGGATGAGTT | 55130 |
| rs11006744 | snp | A/C | 0.499732 | 0.0115784 | intron-variant | ARMC4 | GRCh38.p7 | 10:27852178 | TACCAGGAAAGTTAA[A/C]AGTCTTCTAGGCAGA | 55130 |
| rs11006745 | snp | C/T | 0.499741 | 0.0113788 | intron-variant | ARMC4 | GRCh38.p7 | 10:27857121 | TGGATTTTCTTCAGC[C/T]TCTGCCACTCCTGAG | 55130 |
| rs11006746 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27860457 | gaccttgtttaaaaa[A/G]aaaaaaaaaGTCATG | 55130 |
| rs11006747 | snp | A/C | 0.499928 | 0.00598999 | intron-variant | ARMC4 | GRCh38.p7 | 10:27862006 | TCTGGATAAACAATG[A/C]AATGATTGCCAAAGT | 55130 |
| rs11006748 | snp | A/G | 0.0501905 | 0.150254 | intron-variant | ARMC4 | GRCh38.p7 | 10:27863512 | CAAGTAAATTTGAGC[A/G]AGTAGGCAAATTCCC | 55130 |
| rs11006749 | snp | A/G | 0.497182 | 0.037434 | intron-variant | ARMC4 | GRCh38.p7 | 10:27868354 | AAAGGAATATAAATC[A/G]TTCTATTATAAAGAC | 55130 |
| rs11006750 | snp | C/T | 0.497271 | 0.0368399 | intron-variant | ARMC4 | GRCh38.p7 | 10:27868390 | CACACATATGTTTAT[C/T]GCAGCACTATTCACA | 55130 |
| rs11006751 | snp | A/C | 0.44333 | 0.158505 | intron-variant | ARMC4 | GRCh38.p7 | 10:27870656 | gatggtttccagctt[A/C]atccatgtccctaca | 55130 |
| rs11006752 | snp | C/T | 0.448963 | 0.151372 | intron-variant | ARMC4 | GRCh38.p7 | 10:27871907 | GAAAGTCATTGGTAG[C/T]TTCATGGAGATGGTA | 55130 |
| rs11006753 | snp | A/G | 0.446118 | 0.155041 | intron-variant | ARMC4 | GRCh38.p7 | 10:27873548 | CCCAGAGATTCTGGT[A/G]TGTTGTGTCTTTGTT | 55130 |
| rs11006755 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27882512 | CCTCCATAACAAAAA[A/G]AACACAGGCAAAAAG | 55130 |
| rs11006756 | snp | A/G | 0.442791 | 0.15916 | intron-variant | ARMC4 | GRCh38.p7 | 10:27886378 | gattacatatttaaa[A/G]tgataataaaactat | 55130 |
| rs11006758 | snp | A/G | 0.494057 | 0.0541878 | intron-variant | ARMC4 | GRCh38.p7 | 10:27892258 | GACATAACACAGAAA[A/G]GATCTTAAATGGTAA | 55130 |
| rs11006759 | snp | C/T | 0.4628 | 0.13121 | intron-variant | ARMC4 | GRCh38.p7 | 10:27892653 | ACAAAAAGGTCAATA[C/T]TTCTTATTACAAAAA | 55130 |
| rs11006760 | snp | C/T | 0.463126 | 0.13068 | intron-variant | ARMC4 | GRCh38.p7 | 10:27895118 | gatttttttaatttg[C/T]ttttctttagtttct | 55130 |
| rs11006761 | snp | C/T | 0.462363 | 0.131916 | intron-variant | ARMC4 | GRCh38.p7 | 10:27895142 | agtttctaaaactta[C/T]ataatgaacatgtaA | 55130 |
| rs11006762 | snp | C/T | 0.462582 | 0.131564 | intron-variant | ARMC4 | GRCh38.p7 | 10:27895513 | GGCTGGGTCTTGAAC[C/T]CCTGGCTTCCAGCTA | 55130 |
| rs11006764 | snp | A/G | 0.493613 | 0.0561475 | intron-variant | ARMC4 | GRCh38.p7 | 10:27898852 | TTTAATTTTTTGGCT[A/G]TGATAACAAATGATT | 55130 |
| rs11006765 | snp | A/G | 0.463234 | 0.130503 | intron-variant | ARMC4 | GRCh38.p7 | 10:27898921 | CACACATTACAATTC[A/G]CTTTTTAAAAAATAT | 55130 |
| rs11006766 | snp | A/G | 0.462363 | 0.131916 | intron-variant | ARMC4 | GRCh38.p7 | 10:27900698 | CTGAATCGATCAGGC[A/G]GAAGAAAGGTTATCA | 55130 |
| rs11006767 | snp | A/C | 0.463234 | 0.130503 | intron-variant | ARMC4 | GRCh38.p7 | 10:27900782 | AAGAATGAAAAGGAA[A/C]GAATGAAGCCTCCAA | 55130 |
| rs11006768 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ARMC4 | GRCh38.p7 | 10:27902069 | AAGTAAAACACTCCC[C/T]AGCAAATGCAAAAGA | 55130 |
| rs11006769 | snp | A/G | 0.493837 | 0.055168 | intron-variant | ARMC4 | GRCh38.p7 | 10:27903727 | GAATAAAATACCTAG[A/G]AATAGGGCCATCTGA | 55130 |
| rs11006770 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27916580 | CGCCTCTTCTTCCTC[C/T]TCCTCCTCAGCCTGT | 55130 |
| rs11006771 | snp | A/G | 0.00484259 | 0.0489678 | intron-variant | ARMC4 | GRCh38.p7 | 10:27924724 | TTTAAACACCATTAA[A/G]AGATTAGTTTGCAGG | 55130 |
| rs11006772 | snp | A/G | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27924919 | TATAATTGCATAGGA[A/G]ACTTCTACCAAACCT | 55130 |
| rs11006774 | snp | C/T | 0.452965 | 0.145963 | intron-variant | ARMC4 | GRCh38.p7 | 10:27930048 | GGTTCCatatttata[C/T]atttttctattaaca | 55130 |
| rs11006775 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27930859 | GCATTCAAACAGTCA[A/G]TCTGGTTTACTCTAA | 55130 |
| rs11006776 | snp | A/G | 0.291235 | 0.246576 | intron-variant | ARMC4 | GRCh38.p7 | 10:27935634 | TCAAATGCATCAAAC[A/G]TGGCTCTATTGTACC | 55130 |
| rs11006777 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27936524 | AGTGCCACTGAGGCA[C/G]AGAAAAAGTCATTGC | 55130 |
| rs11006778 | snp | A/G | 0.475789 | 0.107327 | intron-variant | ARMC4 | GRCh38.p7 | 10:27939108 | TTAGTGTAGATTACA[A/G]TAAGTAAACCAGTAA | 55130 |
| rs11006779 | snp | C/T | 0.49934 | 0.0181589 | intron-variant | ARMC4 | GRCh38.p7 | 10:27941657 | TTAAGGGAAAGGCAA[C/T]TTACTATAAGGATTA | 55130 |
| rs11006781 | snp | A/G | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27948908 | TTTTAAACGTGCAGA[A/G]ATTGAATGAAAGTCG | 55130 |
| rs11006782 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27952098 | aaaaaaaaaaGACAC[A/C]CTAACAGAAAATAAA | 55130 |
| rs11006783 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | ARMC4 | GRCh38.p7 | 10:27954342 | TGCAAATACATGGGG[C/T]AAGAAATTCCCCGAA | 55130 |
| rs11006784 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27955448 | ACAACCAGGCAATGT[G/T]CAATAAAGATAGAAG | 55130 |
| rs11006785 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | ARMC4 | GRCh38.p7 | 10:27958398 | ATGTTCACTGGGAGG[A/G]TATTATTGAGGCTGT | 55130 |
| rs11006786 | snp | A/C | 0.48546 | 0.0840147 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27960204 | TGCATTGATGTTGGT[A/C]AAATCATTAGGAGCC | 55130 |
| rs11006787 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | ARMC4 | GRCh38.p7 | 10:27961854 | AGGATTACTTAAGGC[C/G]AAGAGTTCAACACCA | 55130 |
| rs11006788 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27965345 | TCTGAAGGAGAACAG[C/G]TGCTGTCACTGAAAA | 55130 |
| rs11006789 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27969372 | ACGTTGCAACAGGGC[C/G]TGCACCTGGTTTTCC | 55130 |
| rs11006790 | snp | G/T | 0.499575 | 0.0145705 | intron-variant | ARMC4 | GRCh38.p7 | 10:27973406 | aactcatgtcacagg[G/T]gtttgctgtacagat | 55130 |
| rs11006791 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27981018 | AAATTCTGATACATG[C/T]TATAGCATGGATGAG | 55130 |
| rs11006793 | snp | G/T | 0.0539704 | 0.155153 | intron-variant | ARMC4 | GRCh38.p7 | 10:27986927 | GGGAGACTATTAAAG[G/T]CTGTCTCTGCTAAAG | 55130 |
| rs11006794 | snp | C/T | 0.0818113 | 0.184966 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997495 | AGTCAACATACCATA[C/T]AGTAACTTCTTGAAG | 55130 |
| rs11330909 | in-del | -/A | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27965459 | GAGGTGGGGGCAAGG[-/A]AAAAAATGTAGAAGA | 55130 |
| rs11335874 | in-del | -/A | 0.0562307 | 0.157967 | intron-variant | ARMC4 | GRCh38.p7 | 10:27822515 | GCACAACCCAGTAAC[-/A]AGAAATGCCTTTGGA | 55130 |
| rs11371318 | in-del | -/A/AA/AAA | 0.470715 | 0.117409 | intron-variant | ARMC4 | GRCh38.p7 | 10:27941500 | CGAACCAAAAAAAAG[-/A/AA/AAA]AAAAAAAAAAAACCA | 55130 |
| rs11376464 | in-del | -/A | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27908763 | AGTTTACCAGGGGGG[-/A]AAAAATGTATTATTC | 55130 |
| rs11417465 | in-del | -/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27966129 | GGCACAGAGAGCCCC[-/C]AATTTTTGCACTTCC | 55130 |
| rs11423112 | in-del | -/A/AA | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27941512 | AAGAAAAAAAAAAAA[-/A/AA]CCATGAGATCTCTTT | 55130 |
| rs11451204 | in-del | -/T/TT/TTT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27948779 | CTGTTGGCCTTTGGA[-/T/TT/TTT]TTTTTTTTTTTTTTT | 55130 |
| rs11492473 | snp | C/G | 0.453209 | 0.145623 | intron-variant | ARMC4 | GRCh38.p7 | 10:27901438 | AGCTAGCATCAAAAT[C/G]ACAGGATCAAATTCA | 55130 |
| rs11591727 | snp | C/T | 0.309154 | 0.242901 | intron-variant | ARMC4 | GRCh38.p7 | 10:27980641 | acttcacactgacta[C/T]gatgtttataattaa | 55130 |
| rs11592099 | snp | C/G | 0.45235 | 0.146814 | intron-variant | ARMC4 | GRCh38.p7 | 10:27956441 | TCAGGAATAAGACCG[C/G]CTGGATGAAGCATTT | 55130 |
| rs11592848 | snp | C/T | 0.453087 | 0.145793 | intron-variant | ARMC4 | GRCh38.p7 | 10:27942996 | TATCCAACAGGTATT[C/T]ATTAACCGTTCATAC | 55130 |
| rs11593370 | snp | A/C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27988589 | gggatccacacacct[A/C/T]gacctcccaaagtac | 55130 |
| rs11594652 | snp | A/C | 0.49962 | 0.0137727 | intron-variant | ARMC4 | GRCh38.p7 | 10:27832533 | TGTTCACACACACAC[A/C]CAGACACACACACAC | 55130 |
| rs11594736 | snp | A/G | 0.45235 | 0.146814 | intron-variant | ARMC4 | GRCh38.p7 | 10:27955509 | TCTGTGTGGCCTGGA[A/G]CAAAGAATTTCTCAG | 55130 |
| rs11595397 | snp | A/G | 0.494568 | 0.0518327 | intron-variant | ARMC4 | GRCh38.p7 | 10:27891741 | TAAGCACTATCTTGC[A/G]ATATTCACAAAACAA | 55130 |
| rs11595783 | snp | A/C | 0.46137 | 0.133501 | intron-variant | ARMC4 | GRCh38.p7 | 10:27891774 | AATATTAAAAATGCA[A/C]TGATATTTAAGAAAA | 55130 |
| rs11595811 | snp | A/G | 0.499642 | 0.0133738 | intron-variant | ARMC4 | GRCh38.p7 | 10:27979923 | agtactaaaaaacaa[A/G]aacaaagttggagga | 55130 |
| rs11595836 | snp | C/T | 0.483418 | 0.0895317 | intron-variant | ARMC4 | GRCh38.p7 | 10:27852885 | agaatcgcttgaacc[C/T]gggaggtggaagttg | 55130 |
| rs11596093 | snp | A/C | 0.496905 | 0.0392151 | intron-variant | ARMC4 | GRCh38.p7 | 10:27850290 | TCTCTATCAAAAACA[A/C]AAAAATTAGACGGCC | 55130 |
| rs11596317 | snp | A/G | 0.4941 | 0.0539917 | intron-variant | ARMC4 | GRCh38.p7 | 10:27956105 | AATTTGATGATACAG[A/G]ACAAACAAATTAGGC | 55130 |
| rs11596400 | snp | A/G | 0.452473 | 0.146644 | intron-variant | ARMC4 | GRCh38.p7 | 10:27956491 | CAACTGTGCTTGCCA[A/G]TATAACCCTTGTTGA | 55130 |
| rs11596448 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27885803 | tatataatatatata[A/T]aatatatattatata | 55130 |
| rs11596504 | snp | A/C | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27886111 | acaggaaaattattt[A/C]aagtaataatgacca | 55130 |
| rs11596934 | snp | A/G | 0.45235 | 0.146814 | intron-variant | ARMC4 | GRCh38.p7 | 10:27956961 | CTTCTCCTGTTTCAC[A/G]AAAGGGCTCTCCACC | 55130 |
| rs11596956 | snp | C/T | 0.225893 | 0.248835 | intron-variant | ARMC4 | GRCh38.p7 | 10:27994364 | CTACATCAGAGGTCA[C/T]GAAACCAATGGCTCC | 55130 |
| rs11597108 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27863754 | AAAAAGTTATCCAGC[A/G]TGAAAGGGATTCTGG | 55130 |
| rs11597452 | snp | C/T | 0.221439 | 0.248363 | intron-variant | ARMC4 | GRCh38.p7 | 10:27994754 | ACTGTGTTGGCCAAG[C/T]TGAATATCCTCAGAC | 55130 |
| rs11598344 | snp | A/G | 0.491316 | 0.0653198 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27959591 | GGGAAGTGCAGGAGC[A/G]TGTGGCCTGAATCTA | 55130 |
| rs11599060 | snp | A/G | 0.000308363 | 0.0124132 | missense, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27985023 | AAAAGACTCACAATG[A/G]AATATGTTTTAGAGA | 55130 |
| rs11599349 | snp | C/G | 0.453209 | 0.145623 | intron-variant | ARMC4 | GRCh38.p7 | 10:27943038 | TGGGCTAAGTGCTGT[C/G]AAAGACACTAGGATG | 55130 |
| rs11599390 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27885704 | atatataatatatat[A/T]AAatatatattatat | 55130 |
| rs11599391 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27885706 | atataatatatataa[A/T]atatatattatatat | 55130 |
| rs11812490 | snp | A/C | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27980235 | aggaaaaacacagtg[A/C]taaatttttcatgac | 55130 |
| rs11814132 | snp | A/G | 0.0659589 | 0.169201 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27982984 | AGGTTATTAGGCTCC[A/G]TCATTAGAATCAGCT | 55130 |
| rs11815104 | snp | A/G | 0.127944 | 0.218179 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27960678 | tttttaattgacaaa[A/G]aataattgtatattt | 55130 |
| rs11815183 | snp | C/T | 0.330482 | 0.236691 | intron-variant | ARMC4 | GRCh38.p7 | 10:27955339 | CTGTTGACTCTCACT[C/T]GAATGAAGAAATCCA | 55130 |
| rs11816595 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27928312 | GTCATTCACTTGGTC[C/T]CATCCATTCTCTTCC | 55130 |
| rs11816757 | snp | A/G | 0.4628 | 0.13121 | intron-variant | ARMC4 | GRCh38.p7 | 10:27893052 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 55130 |
| rs11817213 | snp | C/T | 0.0869089 | 0.189476 | intron-variant | ARMC4 | GRCh38.p7 | 10:27955328 | GCAAGGGTTCCCTGT[C/T]GACTCTCACTCGAAT | 55130 |
| rs11817707 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27930013 | AGGAATACCAATTAC[A/G]TTTATGTTGGCTCTC | 55130 |
| rs11818080 | snp | C/T | 0.0912534 | 0.193131 | intron-variant | ARMC4 | GRCh38.p7 | 10:27875840 | gaaaatcgggtcact[C/T]ccaccctaatactgc | 55130 |
| rs11818106 | snp | C/T | 0.100231 | 0.200173 | intron-variant | ARMC4 | GRCh38.p7 | 10:27992013 | CATCACTTGTTCTCA[C/T]AGCAAACACTGAGTG | 55130 |
| rs11818690 | snp | A/G | 0.140581 | 0.224783 | intron-variant | ARMC4 | GRCh38.p7 | 10:27942137 | ctcagaaagcccgta[A/G]catttgtgactgttt | 55130 |
| rs11819711 | snp | G/T | 0.190519 | 0.242821 | intron-variant | ARMC4 | GRCh38.p7 | 10:27964829 | AAAGGTAAGGACCAT[G/T]TCTGTCTTTTATACT | 55130 |
| rs11830620 | snp | C/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872751 | AAAATACTGGCAAAC[C/T]GAATCCAGCAGCACA | 55130 |
| rs11971972 | snp | G/T | 0.375 | 0.216506 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872938 | AAGGAATGGTACCAG[G/T]TCCTCCTTGTACCTC | 55130 |
| rs12098376 | snp | A/G | 0.0475351 | 0.146656 | intron-variant | ARMC4 | GRCh38.p7 | 10:27929898 | ATGTCAATATTACTA[A/G]GATCTTTTGGGGTCT | 55130 |
| rs12098615 | snp | C/T | 0.105924 | 0.204309 | intron-variant | ARMC4 | GRCh38.p7 | 10:27923182 | ccatgaatgtgaatg[C/T]gtttaactcattaaa | 55130 |
| rs12217881 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27864578 | gggagtgaggtgaga[A/G]tggggagtgaggtga | 55130 |
| rs12217989 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27912524 | GCCTGCCCATTGAGG[C/T]CATATATATGAACAA | 55130 |
| rs12218330 | snp | A/G | 0.355096 | 0.226837 | intron-variant | ARMC4 | GRCh38.p7 | 10:27971614 | CCTCTATTGACTAAA[A/G]CACATCGTATTTAAA | 55130 |
| rs12220060 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | ARMC4 | GRCh38.p7 | 10:27864561 | ggagtgaggtgagag[C/T]ggggagtgaggtgag | 55130 |
| rs12220076 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | ARMC4 | GRCh38.p7 | 10:27864560 | gggagtgaggtgaga[A/G]cggggagtgaggtga | 55130 |
| rs12221392 | snp | A/G | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27833320 | TAGCACCCGGCAATA[A/G]TCGTACTTCGCAATG | 55130 |
| rs12246884 | snp | C/T | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27933621 | GAACATCAGAGGTAG[C/T]TGGTGGCCAAGTAGA | 55130 |
| rs12248984 | snp | C/G | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27812821 | CTCATGCACTTCTTA[C/G]CTTTCTGGAGCTGAA | 55130 |
| rs12249609 | snp | A/G | 0.084728 | 0.187577 | intron-variant | ARMC4 | GRCh38.p7 | 10:27813622 | ATGATGCCAAAAAAC[A/G]AGGATGATTTGATAA | 55130 |
| rs12250045 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27831357 | GTTATAGACCCAGGA[A/G]AGGCAGAGGGGCTAG | 55130 |
| rs12253393 | snp | A/G/T | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27966415 | GGCAGAGTGAATTAC[A/G/T]TCTACCCAATCACTC | 55130 |
| rs12254183 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27866635 | ctggtgagggcctca[A/G]gaagcttccactcat | 55130 |
| rs12258035 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27868357 | ggaatataaatcgtt[C/T]tattataaagacaca | 55130 |
| rs12261771 | snp | A/G | 0 | 0 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27940604 | CCACCACTGGAATTA[A/G]CATGTTTTCATGAGA | 55130 |
| rs12261776 | snp | A/G | 0 | 0 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27940628 | CATGAGAAGTCTTCA[A/G]CAGCCGAGCCAACAG | 55130 |
| rs12262418 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27820804 | tttttttttttttga[A/T]ggagttttcctcctg | 55130 |
| rs12262964 | snp | C/T | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27946304 | GAAATTCCATACCAG[C/T]TGCCAAACTCCCTCC | 55130 |
| rs12263357 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27875805 | tcctagccaagggaa[G/T]ctgtgagagatggca | 55130 |
| rs12263449 | snp | C/T | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27941120 | CCTCAGCCCAAACAT[C/T]TCAGAAAACTAGCTT | 55130 |
| rs12263496 | snp | C/T | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27941157 | AACCATTAGCACTTT[C/T]TAAGGAGAACTGAAT | 55130 |
| rs12264704 | snp | G/T | 0.0836354 | 0.186609 | intron-variant | ARMC4 | GRCh38.p7 | 10:27822110 | TCTGGTGTAAAAGGC[G/T]TTGATCTTAAGGTTC | 55130 |
| rs12268314 | snp | G/T | 0.0622301 | 0.165053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27873002 | ggacttattttggtt[G/T]gtaggctattaattg | 55130 |
| rs12355297 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27910947 | ccaatcaatatataa[C/G]gttgtttcacgtgta | 55130 |
| rs12355412 | snp | C/T | 0.429987 | 0.173507 | intron-variant | ARMC4 | GRCh38.p7 | 10:27831789 | CTCTGTAGTCCCAGC[C/T]GTGTGTCTTTATGTT | 55130 |
| rs12355413 | snp | C/T | 0.430285 | 0.173197 | intron-variant | ARMC4 | GRCh38.p7 | 10:27831816 | TGTTTGCAGTTGTTC[C/T]ACTCAATGGAGCCTG | 55130 |
| rs12355681 | snp | C/T | 0.456214 | 0.141336 | intron-variant | ARMC4 | GRCh38.p7 | 10:27952554 | ATGCTTGCCCATCCC[C/T]TTTCCCTGACAGGCC | 55130 |
| rs12356262 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | ARMC4 | GRCh38.p7 | 10:27883629 | ttataaacatatttg[C/T]gaaactaaaggaaac | 55130 |
| rs12356786 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27885785 | tatataaaatatata[A/T]tatatataatatata | 55130 |
| rs12357093 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27935825 | gtgcatacatatata[C/T]acacacatatgtatg | 55130 |
| rs12357953 | snp | C/T | 0.499121 | 0.020948 | intron-variant | ARMC4 | GRCh38.p7 | 10:27813168 | TCTTCTCCAAGATCA[C/T]AACTTTCCCACTTCT | 55130 |
| rs12358191 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27885777 | atatatattatataa[A/T]atatatattatatat | 55130 |
| rs12358199 | snp | C/G | 0.462691 | 0.131387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27893016 | TAGCCAGGCATGGGG[C/G]TGCATGCTTGTCCAT | 55130 |
| rs12358283 | snp | A/G | 0.462144 | 0.132269 | intron-variant | ARMC4 | GRCh38.p7 | 10:27893568 | AGACGTTATTTCAAA[A/G]TGATGCCAAATCCTA | 55130 |
| rs12358416 | snp | C/T | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27939348 | AGCAGGTTTCTCTGA[C/T]TTATACAAGTTATCT | 55130 |
| rs12362870 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27873005 | CTTTTTTTGGTTGAT[A/G]AGCTATTAATTATTG | 55130 |
| rs12411354 | snp | C/T | 0.257176 | 0.249897 | intron-variant | ARMC4 | GRCh38.p7 | 10:27974677 | tgatacctccagctt[C/T]ggtctgtttttgttt | 55130 |
| rs12411379 | snp | A/G | 0.23846 | 0.249734 | intron-variant | ARMC4 | GRCh38.p7 | 10:27903755 | TGAGGCCTCCAGTGC[A/G]GTACCTCCTATTAGA | 55130 |
| rs12412406 | snp | C/T | 0.257176 | 0.249897 | intron-variant | ARMC4 | GRCh38.p7 | 10:27973409 | tcatgtcacaggtgt[C/T]tgctgtacagatgat | 55130 |
| rs12412504 | snp | C/T | 0.237593 | 0.249692 | intron-variant | ARMC4 | GRCh38.p7 | 10:27903284 | tcaataaactaatta[C/T]tgatggaatgtatct | 55130 |
| rs12414419 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | ARMC4 | GRCh38.p7 | 10:27813417 | ATTGGCTTAATGCTT[C/T]CTGTCCTTCTTTAGA | 55130 |
| rs12414611 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27922879 | ccactgcactccaac[C/T]tgggcaacaaagtga | 55130 |
| rs12414731 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | ARMC4 | GRCh38.p7 | 10:27822760 | GAGTCAAGGGGCTTG[C/T]CTTTATTGGTGTCTG | 55130 |
| rs12415087 | snp | A/G | 0.316485 | 0.240998 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27982354 | AAAACTTAAAGGGAT[A/G]CTTAGATATCTCCAT | 55130 |
| rs12415609 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | ARMC4 | GRCh38.p7 | 10:27845868 | aattcaacaagaaga[A/G]ctaactatcctaaat | 55130 |
| rs12415974 | snp | C/G | 0.183568 | 0.241012 | intron-variant | ARMC4 | GRCh38.p7 | 10:27906919 | CCTAATGTAGATGAC[C/G]GGTTGATGGGTGGAG | 55130 |
| rs12570208 | snp | A/C | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27894102 | gtgtgcaaatgtgcc[A/C]ctgtgatccagcctg | 55130 |
| rs12572961 | snp | A/C | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27853517 | taccctctcaaaaaa[A/C]ccaagggtgtctata | 55130 |
| rs12573177 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | ARMC4 | GRCh38.p7 | 10:27977337 | tgagaggccaaggtc[A/G]gcagatcacaaggtc | 55130 |
| rs12761287 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27958672 | ACAATAATAATAAGC[A/C]ATAGAAATGATTAtt | 55130 |
| rs12761300 | snp | A/C | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27958694 | ATGATTATTATTGCC[A/C]ACAGTTACTAACTAC | 55130 |
| rs12762554 | snp | A/G | 0.453209 | 0.145623 | intron-variant | ARMC4 | GRCh38.p7 | 10:27937377 | GACTCTTGCTCTGTC[A/G]CCCAAGGTGGAGTGC | 55130 |
| rs12763599 | snp | A/G | 0.325091 | 0.238456 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:28000823 | ATCTGAAGAAGTCCC[A/G]GTCGCCTCTTTCCAA | 55130 |
| rs12766119 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27962727 | ACGTCCCTGCAGAGG[G/T]CCCTCATGCACACGC | 55130 |
| rs12767652 | snp | C/T | 0.45235 | 0.146814 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27959384 | GCCAGTTCTTTTTTT[C/T]TTTCCCCCAGATGAC | 55130 |
| rs12767701 | snp | A/C | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27850033 | ACTAATCAAATGGAC[A/C]CAGCACTAAAGTGAA | 55130 |
| rs12767770 | snp | G/T | 0.097727 | 0.198275 | intron-variant | ARMC4 | GRCh38.p7 | 10:27989358 | atctggggaataaat[G/T]aatGAATAAAATATT | 55130 |
| rs12768418 | snp | A/T | 0.282895 | 0.247826 | intron-variant | ARMC4 | GRCh38.p7 | 10:27918992 | gaaaaagtataatgg[A/T]aaatgtgcaatgctc | 55130 |
| rs12769662 | snp | G/T | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27968657 | TGTTCCTAAACTTAG[G/T]TCACTGCTCTTTGCA | 55130 |
| rs12770419 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27872729 | AGCAGCACATCAAGA[A/G]GCTTATCCACCATGA | 55130 |
| rs12771117 | snp | A/T | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27838481 | AAGAATATATTTCTC[A/T]CAAGTTTAAAGACTG | 55130 |
| rs12771272 | snp | A/C | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27838458 | GGTGTTTCATAATTT[A/C]CAATGGAAAGAATAT | 55130 |
| rs12771348 | snp | C/T | 0.499354 | 0.0179596 | intron-variant | ARMC4 | GRCh38.p7 | 10:27835001 | TTTCACAAGGTCACC[C/T]AGGCCCGACAGAACA | 55130 |
| rs12771813 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27885784 | ttatataaaatatat[A/T]ttatatataatatat | 55130 |
| rs12771925 | snp | A/G | 0.44252 | 0.159487 | intron-variant | ARMC4 | GRCh38.p7 | 10:27835082 | ATCGCGTGGCCCTGC[A/G]TCCTGGCAGGGCAGG | 55130 |
| rs12772278 | snp | C/T | 0.4941 | 0.0539917 | intron-variant | ARMC4 | GRCh38.p7 | 10:27950930 | GTTCAATAAAGTGGA[C/T]ACAAGAGCAGCATTT | 55130 |
| rs12772470 | snp | A/G | 0.455977 | 0.141681 | intron-variant | ARMC4 | GRCh38.p7 | 10:27951091 | acatggaaaaaagct[A/G]ttaaatattactaaa | 55130 |
| rs12773472 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27885749 | atattatgttatata[A/T]aatatatatTTtata | 55130 |
| rs12773654 | snp | A/G | 0.483923 | 0.0882034 | intron-variant | ARMC4 | GRCh38.p7 | 10:27814503 | gtcactgatcttcac[A/G]cttcagccttccacc | 55130 |
| rs12773866 | snp | C/T | 0.257176 | 0.249897 | intron-variant | ARMC4 | GRCh38.p7 | 10:27972627 | aagcaggaatggcca[C/T]attaaaatcagacaa | 55130 |
| rs12773965 | snp | A/T | 0.49975 | 0.0111793 | intron-variant | ARMC4 | GRCh38.p7 | 10:27856700 | CATACTAGAAAACAC[A/T]CAAGAGATTTTGAAG | 55130 |
| rs12774824 | snp | C/G | 0 | 0 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27960391 | tgctcttacctccca[C/G]gctggagtgcaatgg | 55130 |
| rs12774825 | snp | C/G | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27960392 | gctcttacctcccag[C/G]ctggagtgcaatggc | 55130 |
| rs12775651 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27902514 | gaatccaggagctgg[G/T]tttttgaaaacatta | 55130 |
| rs12777329 | snp | A/G | 0.452597 | 0.146474 | intron-variant | ARMC4 | GRCh38.p7 | 10:27948560 | CCTAAGAACATAATT[A/G]TTTACCAATACTTAT | 55130 |
| rs12777433 | snp | C/T | 0.00268855 | 0.0365657 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27985204 | TTTTACTATGGGGTC[C/T]CTGTTAGCTGCCAAA | 55130 |
| rs12777559 | snp | C/T | 0.453697 | 0.14494 | intron-variant | ARMC4 | GRCh38.p7 | 10:27964313 | AGCTGTTCATCTTGG[C/T]TCCTAGATGAGCTGG | 55130 |
| rs12778301 | snp | A/G | 0.45235 | 0.146814 | intron-variant | ARMC4 | GRCh38.p7 | 10:27957509 | AGCAGAAGGCAGAAC[A/G]TAAGTGCTTATCAGT | 55130 |
| rs12778429 | snp | A/G | 0.452597 | 0.146474 | intron-variant | ARMC4 | GRCh38.p7 | 10:27957345 | CCACTAAGGAACCTC[A/G]CCCTCTCCCCTTCAC | 55130 |
| rs12778544 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27924008 | agaaagaaagaaaga[A/G]agaaagaaagaaaga | 55130 |
| rs12779067 | snp | A/G | 0.257176 | 0.249897 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27981980 | GAATTTAACCGTGGA[A/G]AAGCCTACATTTCTG | 55130 |
| rs12779352 | snp | C/G | 0.49423 | 0.0534032 | intron-variant | ARMC4 | GRCh38.p7 | 10:27943545 | TAATCCCAGCACTTT[C/G]GGAGGCCAAGGTGGG | 55130 |
| rs12779664 | snp | C/T | 0.454784 | 0.1434 | intron-variant | ARMC4 | GRCh38.p7 | 10:27964616 | TTGATCTGTTTTCAT[C/T]TTAGGGACCACATAA | 55130 |
| rs12779675 | snp | C/G | 0.458315 | 0.13822 | intron-variant | ARMC4 | GRCh38.p7 | 10:27908597 | GAAAAAAGATAAAGG[C/G]CATCAAAATTCCTTT | 55130 |
| rs12779879 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27935809 | atgtatatatgtatg[G/T]gtgcatacatatata | 55130 |
| rs12780619 | snp | A/T | 0.49703 | 0.0384237 | intron-variant | ARMC4 | GRCh38.p7 | 10:27878420 | TTAAATTAATGGGTA[A/T]GAAATTCCTTCTCTT | 55130 |
| rs12780829 | snp | C/T | 0.475877 | 0.107142 | intron-variant | ARMC4 | GRCh38.p7 | 10:27943496 | CCTTGCTATTAAATA[C/T]ACTTTTCAggctggg | 55130 |
| rs12988313 | snp | A/G | 0.42 | 0.183303 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872883 | CATAAAATGAGTTAC[A/G]GAGGATTCCCTCTTT | 55130 |
| rs13001407 | snp | G/T | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27873076 | ACACCCTCACAAGAC[G/T]AAACCAGGAAGAAGC | 55130 |
| rs13376891 | snp | G/T | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27914263 | tttcagcaatgctga[G/T]tttggtcctttaatt | 55130 |
| rs16927673 | snp | A/G | 0.100231 | 0.200173 | intron-variant | ARMC4 | GRCh38.p7 | 10:27991128 | TTACAGCAAATTTAA[A/G]TTTCATTCTGAGGTG | 55130 |
| rs16928307 | snp | A/T | 0.0287284 | 0.116357 | intron-variant | ARMC4 | GRCh38.p7 | 10:27813329 | CTAAAGGCCATTTAT[A/T]CCTCATCAGGCTGTC | 55130 |
| rs16928310 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | ARMC4 | GRCh38.p7 | 10:27817204 | TTTGGTTATCCTAAC[A/G]CATGGCTTACATGTC | 55130 |
| rs16928362 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | ARMC4 | GRCh38.p7 | 10:27842206 | TTTGTCCATTTACAT[A/G]TTTTTGACCCGTCTC | 55130 |
| rs16928371 | snp | A/G | 0.0143509 | 0.0834837 | intron-variant | ARMC4 | GRCh38.p7 | 10:27860596 | CATTTACCAAACTTG[A/G]ACTAAACCACAAAGT | 55130 |
| rs16928373 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | ARMC4 | GRCh38.p7 | 10:27869172 | ACTAGAAGGAGCACA[A/G]GAACAAATAAAGATA | 55130 |
| rs16928376 | snp | C/G | 0.0494327 | 0.149241 | intron-variant | ARMC4 | GRCh38.p7 | 10:27870204 | ACATTCAGGCATTTC[C/G]CGATCTGGCCCAACC | 55130 |
| rs16928380 | snp | A/C | 0.0494327 | 0.149241 | intron-variant | ARMC4 | GRCh38.p7 | 10:27870281 | CTTTGGCATAGTCTA[A/C]ACTCCAGCCTCCTGG | 55130 |
| rs16928382 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | ARMC4 | GRCh38.p7 | 10:27877429 | GGTCCCATAAGCTTC[C/T]TAATGACTCCTAATC | 55130 |
| rs16928385 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | ARMC4 | GRCh38.p7 | 10:27877474 | ACATTAGGCTCAAAA[C/T]CCTGCAGGTCCCTCT | 55130 |
| rs16928388 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | ARMC4 | GRCh38.p7 | 10:27877630 | GATGGAAAAAGTAAT[C/T]ATTCTGCCAAAACTG | 55130 |
| rs16928411 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | ARMC4 | GRCh38.p7 | 10:27897002 | AATGGCTACAACCAC[A/G]ACCGCCTAATTCCTG | 55130 |
| rs16928444 | snp | C/T | 0.144969 | 0.226867 | intron-variant | ARMC4 | GRCh38.p7 | 10:27988740 | ATTACTTATTACTGA[C/T]GATCTCACTAGAATA | 55130 |
| rs17533396 | snp | A/G | 0.102014 | 0.201495 | intron-variant | ARMC4 | GRCh38.p7 | 10:27938791 | TTTTAGTAGAGACGG[A/G]GTTGCACCATGTTGG | 55130 |
| rs17562079 | snp | A/C/G | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27967823 | CTGAACTCGGGAGGC[A/C/G]GAGGTTGCACTGAGC | 55130 |
| rs17683682 | snp | C/G | 0.282632 | 0.247861 | intron-variant | ARMC4 | GRCh38.p7 | 10:27884337 | TTTTATAAAAGCTTT[C/G]AAAATCAGCTCAGAT | 55130 |
| rs17683743 | snp | A/T | 0.18325 | 0.240924 | intron-variant | ARMC4 | GRCh38.p7 | 10:27892311 | AAAATATGCAGATTA[A/T]TTTTTATGACTAGTT | 55130 |
| rs17750856 | snp | C/T | 0.021333 | 0.101051 | intron-variant | ARMC4 | GRCh38.p7 | 10:27865734 | TTGTTTGCAAACTCA[C/T]AGCCTTAAAAGAAAG | 55130 |
| rs17751027 | snp | C/T | 0.137187 | 0.223099 | intron-variant | ARMC4 | GRCh38.p7 | 10:27892674 | ATTACAAAAATCCCA[C/T]ATTCCATTTGTTTTA | 55130 |
| rs17830306 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ARMC4 | GRCh38.p7 | 10:27827848 | GGTTCACAGGGTCTT[C/T]GGCAGGCTCCAGTGA | 55130 |
| rs28398887 | snp | A/T | 0.0966517 | 0.197444 | intron-variant | ARMC4 | GRCh38.p7 | 10:27849189 | TGGATTAAGAAAATG[A/T]GGCACATATACACCA | 55130 |
| rs28552759 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27993504 | AAATACAAAAAATTA[A/G]CCAGGCGTGGTGGCG | 55130 |
| rs28609962 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27949301 | TGTAGTGGAGGAAAA[A/G]GGTTTTTAACTTTTT | 55130 |
| rs28776270 | snp | C/G | 0.0966517 | 0.197444 | intron-variant | ARMC4 | GRCh38.p7 | 10:27848782 | AAGACATTTATGAAG[C/G]CAATAGACACACGAG | 55130 |
| rs33935473 | in-del | -/AT | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27982163 | TTCTTCCATAACAGA[-/AT]ATATATATATATAAT | 55130 |
| rs33962916 | in-del | -/T/TG/TT | 0.0418186 | 0.138422 | intron-variant | ARMC4 | GRCh38.p7 | 10:27948803 | TTTTTTTTTTTTTTT[-/T/TG/TT]GCAATTGACATTTGG | 55130 |
| rs33977457 | in-del | -/AT/ATAT/TG | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27993959 | TATATATATATATAT[-/AT/ATAT/TG]GTGTGTGTGTGTGTG | 55130 |
| rs33985354 | in-del | -/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27951430 | AATGCAAAGAGAAAA[-/G]TCCAGAAACAAACTC | 55130 |
| rs34021438 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27922153 | AAAAAAAAAAAAAAA[-/A]GAAAGAAAACAAAAG | 55130 |
| rs34024949 | in-del | -/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27876824 | TATATGCATGTTCCC[-/C]TGATGAACTTCTTGA | 55130 |
| rs34026625 | in-del | -/A | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27982528 | ATAAACCAAAGCAAA[-/A]TCTTATTTGTCTACT | 55130 |
| rs34032497 | in-del | -/T | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997016 | CTATGATATTGATTT[-/T]CAGGATAGCAAAGCA | 55130 |
| rs34047066 | in-del | -/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27972647 | AATCAGACAATATCG[-/G]ACTCCAAAGCAAATA | 55130 |
| rs34048210 | in-del | -/AAA | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27895055 | GAAAAAAAAAAAAAA[-/AAA]CTGTTAGCTCTTAAT | 55130 |
| rs34084011 | snp | A/G | 0.495872 | 0.0452455 | intron-variant | ARMC4 | GRCh38.p7 | 10:27945004 | GTTAAGGAACACCGC[A/G]TTCCCATAGAAATGC | 55130 |
| rs34102636 | in-del | -/AA/AAA | 0.488905 | 0.0736498 | intron-variant | ARMC4 | GRCh38.p7 | 10:27935702 | GATAAAAAAAAAAAA[-/AA/AAA]GTCACTCTCAGGTAT | 55130 |
| rs34129633 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27929157 | CAAATGACCCCAAAA[-/A]TCCTACCATACTGAA | 55130 |
| rs34181914 | in-del | -/T | 0.498813 | 0.0243321 | intron-variant | ARMC4 | GRCh38.p7 | 10:27862676 | ACCTACATTTAGGCA[-/T]TTTTTAAGAGGCAGA | 55130 |
| rs34240147 | in-del | -/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27872685 | ATCCCTGGGATGCAA[-/G]GGCTGGTTCAATATA | 55130 |
| rs34242294 | in-del | -/GT | 0.498852 | 0.0239341 | intron-variant | ARMC4 | GRCh38.p7 | 10:27862792 | ATGTATATGTATAAA[-/GT]GTGTGTGTGTACATA | 55130 |
| rs34257961 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27952995 | GTTTTAGACAGCTTT[-/T]ATTGACATATAATTG | 55130 |
| rs34258812 | in-del | -/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27869400 | CCTGAGAGTATACTG[-/G]AAAAGTTATATATTT | 55130 |
| rs34278673 | in-del | -/A | 0.452842 | 0.146134 | intron-variant | ARMC4 | GRCh38.p7 | 10:27923035 | CCACTAGAACAAAAA[-/A]TGCAAACCTTTCTAA | 55130 |
| rs34331050 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27935732 | ACTCTCAGGTATCTT[-/T]CTATATTAACCACTA | 55130 |
| rs34350686 | snp | A/C | 0.452719 | 0.146304 | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27959028 | ACTCAGGACTCTCTT[A/C]ATTCATCTTCTGAAA | 55130 |
| rs34366942 | in-del | -/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27826313 | CAACCAGGCTTCCGG[-/G]ATCATGTACATCCAT | 55130 |
| rs34368206 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27971916 | GACCTGTGCTAGAAA[-/A]TGTTAAATAAAATTA | 55130 |
| rs34381002 | in-del | -/A | 0.449091 | 0.151204 | intron-variant | ARMC4 | GRCh38.p7 | 10:27819834 | AGACCTTATCTCTTT[-/A]AAAAAAAAAAAAAGG | 55130 |
| rs34445453 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27924615 | AAATTGATTAGGAGG[A/G]AAAAAAAAAAAAAAA | 55130 |
| rs34448901 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27907353 | AATGCAGACAAATTT[-/T]CTTATCCCTCAAGAG | 55130 |
| rs34458096 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27868253 | ATTAGTTTAACCATT[-/T]GTGGAAGACAGTGTG | 55130 |
| rs34462779 | snp | C/G | 0.257176 | 0.249897 | intron-variant | ARMC4 | GRCh38.p7 | 10:27970716 | TGCCTGTAATCCCAG[C/G]ATTTTGGGAGGCTGA | 55130 |
| rs34549525 | in-del | -/A | 0.499974 | 0.00359416 | intron-variant | ARMC4 | GRCh38.p7 | 10:27833378 | CCAGGGTACAAACTG[-/A]AAAAAAAAATCAAGG | 55130 |
| rs34554516 | snp | A/G | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872713 | GATGAAGCCCACTTG[A/G]TCATGGTGGATAAGC | 55130 |
| rs34576885 | in-del | -/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27994146 | GTTTGAATGAGATAG[-/C]ATTGAGAGTTCACTG | 55130 |
| rs34603822 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27953200 | CTTCTTAAATGTTTT[-/T]AAGTGCACAATATAT | 55130 |
| rs34640377 | in-del | -/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27873181 | CCACCGATCCCACAG[-/G]AAATACAAACTACCA | 55130 |
| rs34648810 | snp | A/C | 0.444444 | 0.157135 | intron-variant | ARMC4 | GRCh38.p7 | 10:27976214 | GACCATTTCTATTCA[A/C]TTTTTTACTGGTGAT | 55130 |
| rs34649733 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27926005 | GTGAGACTCCAGCTA[-/A]AAAAAAAAAAAAAAA | 55130 |
| rs34651853 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27827820 | CCAATGTCAAATTTT[A/C]ATTCCCCAGAAAGGT | 55130 |
| rs34665104 | snp | C/T | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27854362 | CTCCTAGGTATTTAC[C/T]TAAGAGAAGAGGAAG | 55130 |
| rs34675645 | in-del | -/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27872893 | ATCAATAGAAAATGA[-/G]GGGAATCCTCCCTAA | 55130 |
| rs34717952 | snp | A/G | 0.499437 | 0.0167637 | intron-variant | ARMC4 | GRCh38.p7 | 10:27945002 | AGGTTAAGGAACACC[A/G]CATTCCCATAGAAAT | 55130 |
| rs34735410 | multinucleotide-polymorphism | AT/CA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27903773 | ACCTCCTATTAGATA[AT/CA]GCTGAGGCCCCACCA | 55130 |
| rs34782241 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27818137 | GCCAACGGATCCTGA[-/A]TATTCATATGTCTCT | 55130 |
| rs34787606 | in-del | -/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27917187 | ATATAATATCATCCC[-/C]TGACCTTGTGGTTTT | 55130 |
| rs34805318 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27897024 | AATTCCTGTACTTAA[-/A]TGTACTCTTTTCACT | 55130 |
| rs34859035 | in-del | -/C | 0.463234 | 0.130503 | intron-variant | ARMC4 | GRCh38.p7 | 10:27903548 | TGTATATTTAGAAAA[-/C]CCCATCGTCTCAGCC | 55130 |
| rs34860419 | in-del | -/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27990435 | CCATCTCCACCTTCC[-/C]AAAGTGCTGGGATTA | 55130 |
| rs34872520 | in-del | -/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27878144 | ACCAAGATCATTCCC[-/C]TAAGACAAACAAAAA | 55130 |
| rs34887332 | in-del | -/A | 0.482683 | 0.0914256 | intron-variant | ARMC4 | GRCh38.p7 | 10:27924988 | AAAAAAAAAAAAAAA[-/A]TCCCGATTCCTTTTG | 55130 |
| rs34894124 | in-del | -/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27813842 | GGAAGGGTACTGTAT[-/C]TACTTCATGTAGAGG | 55130 |
| rs34897951 | in-del | -/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27824638 | AATTAAATTATCTAG[-/C]AACGATCCATAGATC | 55130 |
| rs34912878 | in-del | -/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27872861 | CATTTTATGAGGCCA[-/G]GCATCATCCTGATAC | 55130 |
| rs34913381 | in-del | -/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27940836 | ATCCAATGTTCATGG[-/G]AAATCTTAAAAAGAA | 55130 |
| rs34942945 | snp | C/T | 0.257176 | 0.249897 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27981953 | ATGATGTCATAAAAG[C/T]CTTCAAGGTTAGAAT | 55130 |
| rs34944477 | snp | C/T | 0.316726 | 0.240931 | intron-variant | ARMC4 | GRCh38.p7 | 10:27979912 | ATAGCCAAAACAGTA[C/T]TAAAAAACAAAAACA | 55130 |
| rs34954820 | in-del | -/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27872695 | CAGCCTTGCATGGCA[-/G]GGGATGAAGCCCACT | 55130 |
| rs34993894 | in-del | -/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27946225 | ATATAAAAAATACCA[-/C]ATATAAAAATGTATA | 55130 |
| rs35024899 | in-del | -/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27906833 | CACATGGACACAGGG[-/G]AGGGGAACATCACAC | 55130 |
| rs35037793 | in-del | -/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27818594 | AAGAGCTTGATTTCC[-/C]ATACGCAAATGAGAT | 55130 |
| rs35072227 | in-del | -/A | 0.475965 | 0.106957 | intron-variant | ARMC4 | GRCh38.p7 | 10:27829932 | ATTCAGGCAGTAATT[-/A]AAAAAAAAAAAATGT | 55130 |
| rs35084302 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27869714 | AATTTTTGTATTTTT[-/T]AGTAGTGACAGGGTT | 55130 |
| rs35117720 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27955702 | TTTAACCAATTAAGG[-/T]GTGTGTGTGTGTGTG | 55130 |
| rs35166439 | snp | C/T | 0.375 | 0.216506 | intron-variant | ARMC4 | GRCh38.p7 | 10:27873182 | TGGTAGTTTGTATTT[C/T]TGTGGGATTGGTGGT | 55130 |
| rs35181927 | snp | A/C | 0.00465858 | 0.0480374 | missense | ARMC4 | GRCh38.p7 | 10:27860841 | CCTTGCACAGAATAA[A/C]AATAAATTGAGACAT | 55130 |
| rs35182843 | in-del | -/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27842466 | TTAGCAATACATATT[-/G]TTCCTCTGATTACAA | 55130 |
| rs35242712 | snp | C/T | 0.0980639 | 0.198533 | missense | ARMC4 | GRCh38.p7 | 10:27935146 | GAATGCTGCCAAGAA[C/T]GTGAAAACCGAGTCA | 55130 |
| rs35267408 | snp | A/G | 0.49998 | 0.00319482 | intron-variant | ARMC4 | GRCh38.p7 | 10:27814509 | GATCTTCACACTTCA[A/G]CCTTCCACCTTCAGA | 55130 |
| rs35280610 | snp | C/T | 1.64822e-05 | 0.00287068 | missense | ARMC4 | GRCh38.p7 | 10:27935125 | AACCGAGTCATTGTC[C/T]GGAAATGTGGTGGCA | 55130 |
| rs35297178 | in-del | -/C | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27982730 | GGACTTGGATCCTCC[-/C]TTGTAGAATTTTGTT | 55130 |
| rs35313855 | in-del | -/A/AA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27977401 | ACCCCATTTCTGCTA[-/A/AA]AAAAAAAAAAAAAAA | 55130 |
| rs35321010 | in-del | -/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27877302 | TGGGGCCATACTGGG[-/G]AAAAATGACAAAAGT | 55130 |
| rs35362800 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27864832 | CCCAACGGCGTATCA[G/T]GCATGGTACTACGCA | 55130 |
| rs35378756 | in-del | -/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27949436 | GCATCACTCACAGGG[-/G]AAAGAACATCTGAAC | 55130 |
| rs35386710 | in-del | -/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27814731 | GATTGCATAGTCCGT[-/G]CTTTTGAATCATTCT | 55130 |
| rs35399687 | in-del | -/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27872683 | CGTATATTGAACCAG[-/C]CCTTGCATCCCAGGG | 55130 |
| rs35426773 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27929355 | TGAAAGATGATAAAA[-/A]TTTGCATACTTACAC | 55130 |
| rs35446992 | in-del | -/A | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27982508 | TTCGTTTTTCTAAAA[-/A]TATCATAAACCAAAG | 55130 |
| rs35449629 | in-del | -/A | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27909842 | AAAAAAAAAAAAAAA[-/A]GACTCAGAACACTAC | 55130 |
| rs35470255 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ARMC4 | GRCh38.p7 | 10:27895688 | TGGCTAGTAGTTGCC[A/G]TATCTGAACAATACC | 55130 |
| rs35472668 | snp | A/G | 0.0995155 | 0.199813 | missense | ARMC4 | GRCh38.p7 | 10:27939997 | CCTAGGAAAACTACC[A/G]GGCTGCAATCAAAGC | 55130 |
| rs35487545 | in-del | -/G | | | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27857625 | CTAAAATTCAAACTG[-/G]ACTATTCAAACTGAA | 55130 |
| rs35502713 | snp | A/C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | ARMC4 | GRCh38.p7 | 10:27811824 | GTGAGAAATAAAACA[A/C/T]ACAATTGTTTATGCT | 55130 |
| rs35521919 | in-del | -/T | | | frameshift-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27936730 | CTTCTCTTACTTGGT[-/T]AACATTCTCTTTGCT | 55130 |
| rs35526986 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27976220 | TTCTATTCAATTTTT[-/T]ACTGGTGATTCCAGC | 55130 |
| rs35527160 | in-del | -/T | | | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27936718 | AATATTGAGAGCCTT[-/T]CTCTTACTTGGTAAC | 55130 |
| rs35535377 | snp | C/G | 0.257176 | 0.249897 | intron-variant | ARMC4 | GRCh38.p7 | 10:27979126 | GAGGCACGAGAATCA[C/G]TTGAACCCGGGAGGG | 55130 |
| rs35544223 | in-del | -/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27934027 | GGGCAGGTCTTTCCC[-/C]ATGCTGTTCTCATGA | 55130 |
| rs35583813 | in-del | -/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27917234 | CAACATGGGATCTGG[-/G]AAAATAACCAGTTTT | 55130 |
| rs35586768 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27877997 | TTGTTTAACATTTTT[-/T]CACTATACACTGTGC | 55130 |
| rs35594396 | in-del | -/T | 0.448066 | 0.152544 | intron-variant | ARMC4 | GRCh38.p7 | 10:27948247 | GAGGGATTTTTTTTT[-/T]AGAACAGTTTTATAT | 55130 |
| rs35635880 | in-del | -/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27854953 | ATTTTTCTTAAGTTC[-/C]TAGAAAATGAAAACT | 55130 |
| rs35697488 | in-del | -/AG/CA/CAAA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27979472 | ACACACACACACACA[-/AG/CA/CAAA]GAGTTAAATGAATTC | 55130 |
| rs35735652 | in-del | -/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27974690 | GTTTTTTTTTTTTTT[-/T]GCTTAGGATTGCCTT | 55130 |
| rs35741031 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27952970 | AGTGTGCATATATTG[G/T]TTTTCTCTTTGTTTT | 55130 |
| rs35752745 | in-del | -/T | | | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:28000931 | CTTTTTTTTTTTTTT[-/T]GAGACGAGGTCTCAT | 55130 |
| rs35782656 | in-del | -/T | 0.499598 | 0.0141716 | intron-variant | ARMC4 | GRCh38.p7 | 10:27869541 | TCTTTTTTCTTTTTC[-/T]TTTTTTTTTTTGAGA | 55130 |
| rs35844209 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27943768 | CCACTGCACTCCAGC[C/T]TGAGCCACAGAAGTG | 55130 |
| rs35865039 | snp | C/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27873225 | AAAGAATCAAATAGA[C/T]GCAATAAAAAATGAT | 55130 |
| rs35966490 | in-del | -/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27872722 | AGTTGATCATGGTGG[-/G]ATAAGCTTTTTGATG | 55130 |
| rs35969112 | snp | C/T | 0.256619 | 0.249912 | intron-variant | ARMC4 | GRCh38.p7 | 10:27975998 | ACTTGAAAAATTAAT[C/T]AAAGCAATTAATCAC | 55130 |
| rs35987811 | snp | A/G | 0.257176 | 0.249897 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27982907 | AAGCCCAGCCACCCA[A/G]CCTCTACTTTGTGCT | 55130 |
| rs36017283 | in-del | -/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27936258 | GTTACAAATACTTTA[-/G]AAATCGAATCTGATG | 55130 |
| rs36020867 | snp | A/C | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872855 | GGCTTTGGTATCAGG[A/C]TGATGCTGGCCTCAT | 55130 |
| rs36033174 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27910548 | TCGCATGAGCTCAAG[-/T]AGTTCAAGACTAGCC | 55130 |
| rs36040897 | in-del | -/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27823559 | TAAGATAGATATGGG[-/G]ATTAAATGGGAAACG | 55130 |
| rs36066472 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27820883 | GACTCCCGGATTCAA[-/A]GCCATTCTCCTGCCT | 55130 |
| rs36092482 | in-del | -/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27979791 | TGGCAATACTATGTA[-/G]AAGCAATTCATAAAT | 55130 |
| rs36111729 | in-del | -/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27985526 | TCAGAATGCACATTC[-/C]AATTAATACATTCAG | 55130 |
| rs36115174 | in-del | -/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27916082 | GCAACCCAACGCGGG[-/G]AAGTCAGAACCCTAG | 55130 |
| rs36126736 | in-del | -/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27853373 | TCTGTCTATAAATAA[-/C]ATAAATAAATAAATA | 55130 |
| rs36170986 | snp | A/T | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872929 | TAGTTTCAGAAGGAA[A/T]GGTACCAGTTCCTCC | 55130 |
| rs41283706 | snp | C/G | 0.148928 | 0.228658 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944803 | CCGCATCCAAGGTGA[C/G]AGAGCCACTCACCTT | 55130 |
| rs41283708 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27957689 | TGAAAAGAATTTATA[A/C]ATATATAAAACTTGC | 55130 |
| rs41283710 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27969127 | CCATGTGCTCAAATG[A/T]TGCGTGTTCCTGACA | 55130 |
| rs41283712 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27969179 | CACTCGGAGCTGTCT[C/T]TTTCACTCTTTCAGC | 55130 |
| rs41306318 | snp | C/G | 0.0832709 | 0.186283 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:28000163 | CACCATGTTGGCCAG[C/G]TGGGTCTTGAACTCC | 55130 |
| rs45576735 | snp | C/T | 0.0221141 | 0.102801 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997589 | AATGTAACATTTGAA[C/T]CTATTCAAATTGTAT | 55130 |
| rs45583137 | snp | A/G | 0.211212 | 0.246973 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997351 | ATCTTATACAGAAAG[A/G]CTTAGGTGAAAGTTC | 55130 |
| rs55671233 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27855672 | GCTTCAAAAACGATG[A/G]GTGTGTTTGCGTCTG | 55130 |
| rs55682903 | in-del | -/ATATATAT | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27827405 | TATATATATATATAT[-/ATATATAT]TCCATGTTTCTGCTT | 55130 |
| rs55716902 | snp | A/C | 0.030665 | 0.119967 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984433 | CTATAATTTTATAAC[A/C]GCACTGTCAACACAT | 55130 |
| rs55811996 | in-del | -/AT/TA | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27982164 | GAATATATATATATA[-/AT/TA]ATGTATACACACATC | 55130 |
| rs55829732 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27849778 | TGAAAAAATAGTTCC[C/T]AATGGGTTTCATAAA | 55130 |
| rs55905715 | in-del | -/TTAAT | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27891955 | TTAAGAACAAAGAAT[-/TTAAT]ATATGGATTTTTACC | 55130 |
| rs55937906 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27876573 | CCCACTTAGCCCTGC[A/G]AACTCTAACTCAACT | 55130 |
| rs55940325 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27828232 | CTAGGAGCAGCTGGG[A/G]CAAGGAGGCTCTTGA | 55130 |
| rs55974661 | snp | A/C | 0.0718919 | 0.175435 | intron-variant | ARMC4 | GRCh38.p7 | 10:27832509 | GCTCAACTTTCCCCC[A/C]ACCCATGTTGTTCAC | 55130 |
| rs55982266 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27944093 | TTAAGGGCAAGCGAT[A/G]CAGACAGAAGGCTCC | 55130 |
| rs56017872 | in-del | -/GT/GTGT | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27994009 | TGTGTGTGTGTGTGT[-/GT/GTGT]ATTTGTTAGCTTACT | 55130 |
| rs56031733 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27819601 | AAAAAAAAAAAAAAA[-/A]GTTAACCAGACATAG | 55130 |
| rs56034316 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27934565 | AATAAGGAGCAACAC[C/T]ATTACTTAAAATTCT | 55130 |
| rs56059926 | in-del | -/AAAAAAAAAAAA | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27943818 | AAAAAAAAAAAAAAA[-/AAAAAAAAAAAA]GGCATCATAGATGTC | 55130 |
| rs56086075 | snp | A/T | 0.0707826 | 0.174302 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997894 | ACCTTTGAAGTAAAG[A/T]AAGTAAGTTTAAAGA | 55130 |
| rs56121574 | snp | A/G | 0.162581 | 0.234218 | intron-variant | ARMC4 | GRCh38.p7 | 10:27915329 | AGGCTGGGAAGTCAA[A/G]GATAAAGGCAGGCAG | 55130 |
| rs56137930 | in-del | -/C | 0.469544 | 0.119585 | intron-variant | ARMC4 | GRCh38.p7 | 10:27858654 | AACTGTGTGGGTGGG[-/C]CAAACACAGTTTGGT | 55130 |
| rs56146565 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27907360 | GACAAATTTCTTATC[C/T]CTCAAGAGACAAGAA | 55130 |
| rs56197094 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27846995 | ATTCTACCAGAAGTA[C/T]AAGGAGGAGCGGGGA | 55130 |
| rs56222765 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27864944 | GGCTCAAAGAGGTTG[A/G]ACCTTATAAAATAGA | 55130 |
| rs56230953 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27837315 | TGATAAAGACAGTTA[A/G]TTCCCAAGGAGGTTT | 55130 |
| rs56239581 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27926718 | AGTAAAGATCCTGAG[A/G]TATGGAAAAATAAAT | 55130 |
| rs56240808 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27818709 | ACCTAATATCTACCT[C/T]TCATGGCCACCCGCC | 55130 |
| rs56253410 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27915776 | CTTAGCCCTAAAGCC[A/G]GTAAGTGGAGCACAC | 55130 |
| rs56265853 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27995391 | TTAAGAAATTTCCGG[G/T]ATTTGCCCTGAAATT | 55130 |
| rs56306940 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27888984 | AACATCCAAAGCACA[A/G]TGTAGCTGAAGTTCT | 55130 |
| rs56335062 | snp | A/T | 0.0704125 | 0.17392 | intron-variant | ARMC4 | GRCh38.p7 | 10:27975562 | CCTTTAAGACAATCT[A/T]ATCTACCAAAGCTCC | 55130 |
| rs56351836 | snp | G/T | 0.0433465 | 0.140692 | intron-variant | ARMC4 | GRCh38.p7 | 10:27849053 | CATCCCATTACTGGG[G/T]ATATACCCAAAGGAT | 55130 |
| rs56352562 | snp | A/G | 0.0640965 | 0.167152 | intron-variant | ARMC4 | GRCh38.p7 | 10:27869696 | CATGCCACCATGTCC[A/G]GCTAATTTTTGTATT | 55130 |
| rs56354437 | in-del | -/C | 0.496999 | 0.0386216 | intron-variant | ARMC4 | GRCh38.p7 | 10:27873062 | TATTGAGGGATTCAA[-/C]TTCTTCCTGGTTTAG | 55130 |
| rs56390356 | in-del | -/ATAC/ATACATACATAC | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27973256 | TACATACATACATAC[-/ATAC/ATACATACATAC]GCTGAGACAGCCAGA | 55130 |
| rs56394728 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27893736 | GCAGTGACGGGGAGA[A/G]AGAAAGGGCTATACT | 55130 |
| rs56731384 | in-del | -/GTGT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27955739 | TGTGTGTGTGTGTGT[-/GTGT]TTAATCAGTTTACAT | 55130 |
| rs56794932 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | ARMC4 | GRCh38.p7 | 10:27891035 | CTTGTGTTTATAGCA[A/G]TATTCCTAGCATGAA | 55130 |
| rs56922968 | in-del | -/A | 0.332106 | 0.236133 | intron-variant | ARMC4 | GRCh38.p7 | 10:27916515 | TGTGTGGGACCACTT[-/A]ACATGTGGGTTTCCT | 55130 |
| rs57009449 | in-del | -/TT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27963636 | GGCCTTATATGAACC[-/TT]AATAATAGACTATTT | 55130 |
| rs57067036 | snp | A/C/G | 0.226233 | 0.249795 | missense, intron-variant | ARMC4 | GRCh38.p7 | 10:27968924 | GACCAGAAACATACC[A/C/G]AAGTAATTGTGCTCT | 55130 |
| rs57133419 | snp | G/T | 0.0832709 | 0.186283 | intron-variant | ARMC4 | GRCh38.p7 | 10:27995445 | AGGGCCTAAGAGAGA[G/T]GATTCAAACAGATAG | 55130 |
| rs57190054 | snp | C/T | 0.0659589 | 0.169201 | intron-variant | ARMC4 | GRCh38.p7 | 10:27930957 | ACTCCGAAATGTCTA[C/T]GAAATGGCTGGAAGG | 55130 |
| rs57244050 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ARMC4 | GRCh38.p7 | 10:27896199 | TACACGTCAATGAAA[C/T]TTTGTCCCTGCATAT | 55130 |
| rs57246433 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | ARMC4 | GRCh38.p7 | 10:27961260 | CCAGCTTTAAAAATC[C/T]ATGTTATTTCTTCCA | 55130 |
| rs57248296 | snp | A/C | 0.0174175 | 0.0916809 | intron-variant | ARMC4 | GRCh38.p7 | 10:27890072 | TGCATAATCAAAAAA[A/C]TGGAGCAAGTACAAT | 55130 |
| rs57290701 | in-del | -/AA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27963637 | GGCCTTATATGAACC[-/AA]TAATAGACTATTTAT | 55130 |
| rs57375404 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27937355 | TTTTTTTTTTTTTTT[-/T]GAGAGAGACTCTTGC | 55130 |
| rs57460326 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27925699 | AGATAATTTTAATAT[G/T]ATAAAATACATACAC | 55130 |
| rs57483828 | snp | C/T | 0.332799 | 0.23589 | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27936330 | TTAGTTGACATTTAG[C/T]TGATTCATCTTGTTT | 55130 |
| rs57643587 | snp | A/C | 0.0667028 | 0.170006 | intron-variant | ARMC4 | GRCh38.p7 | 10:27950975 | ATACACTAACAATAA[A/C]AAATCAAAATGTTTA | 55130 |
| rs57657796 | snp | A/G | 0.143284 | 0.226079 | intron-variant | ARMC4 | GRCh38.p7 | 10:27843986 | CGGAGGATTGCTTGA[A/G]GCTGAGTTCAAGACT | 55130 |
| rs57657838 | in-del | -/GT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27955741 | TGTGTGTGTGTGTGT[-/GT]TTAATCAGTTTACAT | 55130 |
| rs57804974 | in-del | -/AAAT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27970149 | AATAAATAAATAAAT[-/AAAT]CTCTAGGTATTTCTG | 55130 |
| rs57807028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27852189 | TTAAAAGTCTTCTAG[A/G]CAGAAGGAAAATGAT | 55130 |
| rs57814665 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | ARMC4 | GRCh38.p7 | 10:27963899 | AATCTATGAGGTTGT[C/T]ATTACTCTCATTATA | 55130 |
| rs57864525 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27963645 | ATGAACCAATAATAG[A/T]CTATTTATGGTCTTA | 55130 |
| rs57899363 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27925721 | TACATACACTTTAAA[A/C]CTAAGGTTATTCTTT | 55130 |
| rs57951932 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARMC4 | GRCh38.p7 | 10:27860096 | TTATTTTACTAAGTA[C/T]ATTTCTATGCTTTAA | 55130 |
| rs58107550 | snp | C/G | 0.5 | 0 | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27981839 | AGTACCTCCTATATG[C/G]ATGTAAGGCACTCTG | 55130 |
| rs58108383 | in-del | -/ATGT/TATG | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940262 | TAAATGTCAGTATAT[-/ATGT/TATG]GTGATATATATATAA | 55130 |
| rs58190321 | snp | C/T | 0.0766824 | 0.180169 | intron-variant | ARMC4 | GRCh38.p7 | 10:27914280 | TTGGTCCTTTAATTA[C/T]GCTGGTGACCACCAG | 55130 |
| rs58422051 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944710 | AGCAATAATAGCAGA[C/T]AAAGACAAGAACCAG | 55130 |
| rs58502831 | snp | C/T | 0.0905309 | 0.192535 | intron-variant | ARMC4 | GRCh38.p7 | 10:27937154 | AGGCATCTCCTGAGG[C/T]GAAGGTCAGTGGAAA | 55130 |
| rs58628171 | snp | C/T | 0.0667028 | 0.170006 | intron-variant | ARMC4 | GRCh38.p7 | 10:27937238 | AGTCTTGGGAAAACA[C/T]AGTAGAGAAGACAGA | 55130 |
| rs58638553 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | ARMC4 | GRCh38.p7 | 10:27881636 | AGCAAAATCCCGTCT[C/T]AAAAAAACACTGAAA | 55130 |
| rs58716372 | snp | C/T | 0.33303 | 0.235809 | intron-variant | ARMC4 | GRCh38.p7 | 10:27930835 | GAACACGTTGTCATT[C/T]AGTTTTGAGCATTCA | 55130 |
| rs58720058 | snp | C/T | 0.0955749 | 0.196603 | intron-variant | ARMC4 | GRCh38.p7 | 10:27861054 | TGAAGTGCAGTGGTG[C/T]CATCTCAGCTCACTG | 55130 |
| rs58751538 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ARMC4 | GRCh38.p7 | 10:27896039 | CTCTCTCATTTCAAG[C/T]GTTCACTAGACAAGT | 55130 |
| rs58833490 | in-del | -/ATTT | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27893563 | ACAAAGACGTTATTT[-/ATTT]CAAAGTGATGCCAAA | 55130 |
| rs58893031 | in-del | -/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27963639 | CTTATATGAACCAAT[-/G]AATAGACTATTTATG | 55130 |
| rs59088367 | snp | A/G | 0.218151 | 0.247963 | intron-variant | ARMC4 | GRCh38.p7 | 10:27899359 | CACACCACCAAAGCC[A/G]TGGGTTTCAAGCACA | 55130 |
| rs59125275 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27882213 | AAAGAAAGAAAGAAA[A/G]AAAGAAAGAAAGAAA | 55130 |
| rs59235047 | snp | A/C | 0.0640965 | 0.167152 | intron-variant | ARMC4 | GRCh38.p7 | 10:27869982 | ATTGAGTCAAAATGA[A/C]CTTCAAAGTAAAATA | 55130 |
| rs59247264 | snp | C/T | 0.333722 | 0.235565 | intron-variant | ARMC4 | GRCh38.p7 | 10:27914736 | TGTATACACATACTT[C/T]ATATATGTATATAAA | 55130 |
| rs59271137 | snp | A/T | 0.0707826 | 0.174302 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997679 | AAGAAAACCTCAGGG[A/T]GGCCTATGACAATCC | 55130 |
| rs59329138 | snp | A/C | 0.33303 | 0.235809 | intron-variant | ARMC4 | GRCh38.p7 | 10:27930808 | AACAACCTGCAATCC[A/C]TTTCACACTGAGAAC | 55130 |
| rs59540473 | snp | C/T | 0.0955749 | 0.196603 | intron-variant | ARMC4 | GRCh38.p7 | 10:27861079 | TCACTGCAAGCTCGG[C/T]CTCCTGGATTCAAGT | 55130 |
| rs59575242 | in-del | -/AA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27819834 | AGACCTTATCTCTTT[-/AA]AAAAAAAAAAAAGGA | 55130 |
| rs59610152 | snp | C/T | 0.309401 | 0.24284 | intron-variant | ARMC4 | GRCh38.p7 | 10:27899302 | ACTACACTTTTCCCA[C/T]GGTCTTTGCAACCCG | 55130 |
| rs59727990 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | ARMC4 | GRCh38.p7 | 10:27845963 | ACTTAGGCTCCCACA[C/T]AATAATAATGGGAGA | 55130 |
| rs59741264 | snp | A/G | 0.093417 | 0.194889 | intron-variant | ARMC4 | GRCh38.p7 | 10:27873936 | CTGTCTCGTTGATCC[A/G]TCTAATGTTGACAGT | 55130 |
| rs59779726 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | ARMC4 | GRCh38.p7 | 10:27839559 | ACTTGGAAATATTAT[C/T]GTTACTAATGTTATT | 55130 |
| rs59829710 | snp | A/C | 0.134119 | 0.221521 | intron-variant | ARMC4 | GRCh38.p7 | 10:27874224 | TAGATCTTCCTCCAT[A/C]CCTTTATTTTGAGCC | 55130 |
| rs59977029 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27909809 | GGCGACAAAGTGAGT[C/T]TTCATTTGAAAAAAA | 55130 |
| rs60016736 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | ARMC4 | GRCh38.p7 | 10:27965295 | GCCTACGGTCCCCAT[A/G]CCCTGTGGTTACACA | 55130 |
| rs60111960 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27963643 | ATATGAACCAATAAT[A/T]GACTATTTATGGTCT | 55130 |
| rs60226782 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27924640 | AAAAAAAAAAAAAAA[-/A]CAGAAGAAAGCCCAC | 55130 |
| rs60249097 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | ARMC4 | GRCh38.p7 | 10:27998595 | ACGGTCCCCAACCTA[A/G]GGCCGAGGCAGGGTC | 55130 |
| rs60344337 | in-del | -/AA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27930640 | CAAAAAAAAAAAAAA[-/AA]GAAAAAGAAAAAGGC | 55130 |
| rs60559154 | snp | C/G | 0.0414363 | 0.137845 | intron-variant | ARMC4 | GRCh38.p7 | 10:27915063 | CCCCCAAATTGATGG[C/G]AGACATTAATCCATA | 55130 |
| rs60648256 | snp | C/T | 0.141596 | 0.225274 | intron-variant | ARMC4 | GRCh38.p7 | 10:27933654 | TGGGTAGACAAAAAA[C/T]AAAGAGGAACCAAAG | 55130 |
| rs60666079 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27963649 | ACCAATAATAGACTA[A/T]TTATGGTCTTAATTC | 55130 |
| rs60695014 | snp | C/T | 0.331874 | 0.236213 | intron-variant | ARMC4 | GRCh38.p7 | 10:27930702 | CTTATTAAGAAACAA[C/T]ATACTGTTTTAACAG | 55130 |
| rs60695807 | snp | C/T | 0.33303 | 0.235809 | intron-variant | ARMC4 | GRCh38.p7 | 10:27929081 | GTTAAACAAGAAATT[C/T]GATTGTGTAAAGGTG | 55130 |
| rs60775313 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | ARMC4 | GRCh38.p7 | 10:27909360 | AAATTTCACAATTAA[C/T]TTTAAAACAAGTTAT | 55130 |
| rs60814150 | snp | C/T | 0.0659589 | 0.169201 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27982243 | TTTGTTATATATAAC[C/T]GTATACACAAAAACA | 55130 |
| rs60815059 | snp | G/T | 0.179744 | 0.239925 | intron-variant | ARMC4 | GRCh38.p7 | 10:27965286 | GAGATTTCTGCCTAC[G/T]GTCCCCATGCCCTGT | 55130 |
| rs60839420 | snp | A/T | 0.0193772 | 0.0965046 | intron-variant | ARMC4 | GRCh38.p7 | 10:27869533 | CTTTTTTTTCTTTTT[A/T]CTTTTTCTTTTTTTT | 55130 |
| rs60857634 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940181 | TATACACATATGTGT[A/G]TTTGTGTGTGTGTAT | 55130 |
| rs60972647 | snp | G/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27873034 | TAGACCAATAACAGG[G/T]TCTGAAATTGTGCCA | 55130 |
| rs60989035 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | ARMC4 | GRCh38.p7 | 10:27974255 | GTTGACAGTTTGCTG[A/T]GCAGAAGCTCTGAGG | 55130 |
| rs61049661 | snp | C/T | 0.33303 | 0.235809 | intron-variant | ARMC4 | GRCh38.p7 | 10:27933182 | TTGAGCCCATGAGTT[C/T]GAAGTTGCAGCAAGC | 55130 |
| rs61097928 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | ARMC4 | GRCh38.p7 | 10:27822009 | ACATCATTCAAACAA[A/G]TAACTTTTTACAACA | 55130 |
| rs61124727 | in-del | -/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27907889 | ATTTTTTTTTTTTTT[-/T]GCAAAACTTCATCAA | 55130 |
| rs61160388 | snp | A/T | 0.180064 | 0.240019 | intron-variant | ARMC4 | GRCh38.p7 | 10:27965274 | AGCAATAAAGAGGAG[A/T]TTTCTGCCTACGGTC | 55130 |
| rs61209171 | in-del | -/GACC | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27963649 | CCAATAATAGACTAT[-/GACC]TTATGGTCTTAATTC | 55130 |
| rs61266143 | snp | A/G | | | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27936329 | GTTAGTTGACATTTA[A/G]TTGATTCATCTTGTT | 55130 |
| rs61282722 | in-del | -/C | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872787 | ATATCCTTGATGAAC[-/C]ATTGATGCAAAAATC | 55130 |
| rs61292688 | snp | A/T | 0.292266 | 0.246401 | intron-variant | ARMC4 | GRCh38.p7 | 10:27991607 | TCAATGTCCACAGAG[A/T]CCAACAAAAAAGGGG | 55130 |
| rs61344519 | snp | C/T | 0.0707826 | 0.174302 | intron-variant | ARMC4 | GRCh38.p7 | 10:27972778 | GAAGGAAACACAGAG[C/T]TAAAAGGAAAAGTAG | 55130 |
| rs61380331 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27851901 | TTTCTCCAAACCAGT[A/G]AAAATGATGAAATCT | 55130 |
| rs61394514 | snp | C/T | 0.128976 | 0.218754 | intron-variant | ARMC4 | GRCh38.p7 | 10:27952006 | CTTGAACTGGGGAGG[C/T]AGAGGTTGCAGTGAG | 55130 |
| rs61456649 | snp | A/G | 0.333722 | 0.235565 | intron-variant | ARMC4 | GRCh38.p7 | 10:27914899 | CAAAGAGAAAAGCCT[A/G]ACCTTTTCTCTTTGA | 55130 |
| rs61476792 | snp | A/T | 0.0966517 | 0.197444 | intron-variant | ARMC4 | GRCh38.p7 | 10:27841125 | TGTAATTATTAAGCC[A/T]AATATTCTAATATTG | 55130 |
| rs61534150 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | ARMC4 | GRCh38.p7 | 10:27819274 | AACAGAAATAGAAGG[A/G]ATGAAAAAGGGGGAA | 55130 |
| rs61729351 | snp | C/G | 0.00147389 | 0.0271067 | missense | ARMC4 | GRCh38.p7 | 10:27994938 | CAACATAACCTGATT[C/G]AAATGCTGAGGGCGC | 55130 |
| rs61729354 | snp | A/T | 0.00366971 | 0.0426777 | missense, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27984254 | TTTGAGCAGTTCTAT[A/T]TCCTTCTTCACCGTC | 55130 |
| rs61752511 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27818038 | CTTTGTTATCCTGGA[C/G]TATGGAGTGCCAACT | 55130 |
| rs61842684 | snp | C/T | 0.0524604 | 0.153226 | intron-variant | ARMC4 | GRCh38.p7 | 10:27845488 | AAATGTAAAGACCAT[C/T]GATGCTAGGAAGAAA | 55130 |
| rs61842685 | snp | A/C | | | missense | ARMC4 | GRCh38.p7 | 10:27860791 | ACTCTATTCCTGCCC[A/C]ACATACAGCAACGTG | 55130 |
| rs61842686 | snp | A/C/G | 0.00171066 | 0.0291959 | intron-variant | ARMC4 | GRCh38.p7 | 10:27860882 | TGGGATCTGTGCATT[A/C/G]TAATGACCCTGCAAG | 55130 |
| rs61842705 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ARMC4 | GRCh38.p7 | 10:27903050 | ATGCGAAAATCCTCA[A/G]TAAAATACTGGCAAA | 55130 |
| rs61842706 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27908498 | CCATTGGGTACTCAC[A/G]GCGGAGAAGAAGGCC | 55130 |
| rs61842724 | snp | A/C/T | 0.0744748 | 0.178019 | intron-variant | ARMC4 | GRCh38.p7 | 10:27921734 | ATAAAAATCCCCAGT[A/C/T]CAAAAAAAAAAAAAT | 55130 |
| rs61842725 | snp | A/C | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27922150 | CAGAGTGAAACTCTG[A/C]CTCAAAAAAAAAAAA | 55130 |
| rs61842727 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARMC4 | GRCh38.p7 | 10:27946823 | TTTAAAATAAGAAAC[C/T]GAAATAGGATTGATT | 55130 |
| rs61842728 | snp | A/G | 0.0555428 | 0.157119 | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27958931 | GGTATTCTGCTTCCT[A/G]ATCCATCTTTTGTTT | 55130 |
| rs61842755 | snp | A/G | 0.453939 | 0.144598 | intron-variant | ARMC4 | GRCh38.p7 | 10:27967541 | ATTCCTCACCAGCCT[A/G]GAGAAGCAACACATA | 55130 |
| rs61842758 | snp | C/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27976553 | AGAGATGTATAAGAC[C/T]TGTATATTGAAAGCT | 55130 |
| rs61843168 | snp | C/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27812754 | AAAAGCATAAGAAAT[C/T]CCATTTAAGCAAATA | 55130 |
| rs61843170 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | ARMC4 | GRCh38.p7 | 10:27831068 | GGAGTGGATGGGGGA[A/G]GGAAGAGGCATGAGG | 55130 |
| rs61843171 | snp | C/T | 0.116838 | 0.211584 | intron-variant | ARMC4 | GRCh38.p7 | 10:27832094 | TAACTCAATAAACAG[C/T]ATTTTGAAGTTCAGA | 55130 |
| rs61843211 | snp | A/G | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27834578 | GGGACTGTGCTACGA[A/G]GAAGGATGGTGGGGG | 55130 |
| rs61845064 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | ARMC4 | GRCh38.p7 | 10:27987190 | TCATTTTAAAGCAGA[A/C]ATTTGATAGGAGCAT | 55130 |
| rs61845065 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27993972 | CAAATATATATATAT[A/G]TATGTGTGTGTGTGT | 55130 |
| rs62517407 | snp | C/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27873007 | GGCAATAACCAATAG[C/T]TTACCAACCAAAAAG | 55130 |
| rs66777965 | snp | A/G | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27961240 | GCCTGGAGTTTAACC[A/G]AAGTCCAGCTTTAAA | 55130 |
| rs66841430 | in-del | -/T/TT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27948802 | TGTTGGCCTTTGGAT[-/T/TT]TTTTTTTTTTTTTTT | 55130 |
| rs67555855 | in-del | -/TTAT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27893558 | TCCAAACAAAGACGT[-/TTAT]TATTTCAAAGTGATG | 55130 |
| rs67654019 | snp | A/C | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27924640 | AAAAAAAAAAAAAAA[A/C]CAGAAGAAAGCCCAC | 55130 |
| rs71046383 | in-del | -/TGAAATGAG | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872869 | ATGATGCTGGCCTCA[-/TGAAATGAG]TGAAATGAGTTAGGG | 55130 |
| rs71275378 | snp | C/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27873154 | GCGTAGAGGTGTTTA[C/T]AGTATTCTCTGATGG | 55130 |
| rs71275379 | snp | C/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27873173 | ATTCTCTGATGGTAG[C/T]TTGTATTTCTGTGGG | 55130 |
| rs71388933 | in-del | -/C | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27819784 | TGCTGTTCACTCCTT[-/C]CCTAGAAAAATCACT | 55130 |
| rs71388934 | in-del | -/T | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27824167 | GAACTTATTGAACTA[-/T]TTTTTTTTTTTTTTT | 55130 |
| rs71388937 | in-del | -/A/TTTATTTA | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27853394 | TAGTTAGGGCTTACT[-/A/TTTATTTA]TTTATTTATTTATTT | 55130 |
| rs71388938 | in-del | -/TTTCTTTC/TTTCTTTCTTTCTTTC | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27882236 | ATCAGAGAGTTCATA[-/TTTCTTTC/TTTCTTTCTTTCTTTC]TTTCTTTCTTTCTTT | 55130 |
| rs71388939 | in-del | -/ATTTTATATATAATATATAATATATATTTTATATATAATATATAT | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27885681 | ATATATATTATATAT[lengthTooLong]TATATATATTTTATA | 55130 |
| rs71388941 | in-del | -/TTTATATAT | 0.476574 | 0.105661 | intron-variant | ARMC4 | GRCh38.p7 | 10:27885795 | ATATATTTTATATAT[-/TTTATATAT]ATTATATATAATATA | 55130 |
| rs71388942 | in-del | -/TCTC/TT | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27924011 | CCTTCTTTCTTTCTT[-/TCTC/TT]TCTTTCTTTCTTTCT | 55130 |
| rs71388944 | in-del | -/TTTTTTTTTTTTTT | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27952092 | TTCTGTTAGTGTGTC[-/TTTTTTTTTTTTTT]TTTTTTTTTTTTTTT | 55130 |
| rs71391006 | in-del | -/ATTC | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27970137 | GAGATTTATTTATTT[-/ATTC]ATTTATTTATTTATT | 55130 |
| rs71391007 | in-del | -/GGCGGC | 0 | 0 | upstream-variant-2KB, intron-variant | ARMC4 | GRCh38.p7 | 10:27998946 | AGGCTGGGAGCGGAA[-/GGCGGC]GGCGGCGGCGGCGGC | 55130 |
| rs71487900 | snp | G/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27896102 | ACTTTTGAAAAGCTG[G/T]GTATCTTCTTCATCT | 55130 |
| rs71487902 | snp | A/G | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27924645 | AAAAAAAAAACCAGA[A/G]GAAAGCCCACATTAT | 55130 |
| rs71489603 | snp | A/G | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27924649 | AAAAAACCAGAAGAA[A/G]GCCCACATTATACAA | 55130 |
| rs71489604 | snp | A/G | 0.444444 | 0.157135 | intron-variant | ARMC4 | GRCh38.p7 | 10:27969105 | GTAGATATATACTCC[A/G]TTATTTCCATGTGCT | 55130 |
| rs71489605 | snp | C/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27973477 | ATTTTTTCTGATCTT[C/T]TCCCTCCTCCCACCC | 55130 |
| rs71489606 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | ARMC4 | GRCh38.p7 | 10:27998642 | GTGAGATGGGGCTGG[G/T]AGAGAGAAGGGAAGG | 55130 |
| rs71522871 | in-del | -/G | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872927 | ATAGTTTCAGAAGGA[-/G]ATGGTACCAGTTCCT | 55130 |
| rs71523589 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | ARMC4 | GRCh38.p7 | 10:27827718 | CTCATCTTCCAGCCC[C/T]GTTCCCATCCATTCT | 55130 |
| rs71523590 | in-del | -/A | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27861227 | AACTCCTGGCCTCAA[-/A]GTGATCCACTCACTT | 55130 |
| rs71523591 | in-del | -/TGAA | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27954496 | ATGAATAAACACGAG[-/TGAA]TGAATGAATGAATGA | 55130 |
| rs71523592 | in-del | -/GT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27955697 | CTTTAACCAATTAAG[-/GT]GTGTGTGTGTGTGTG | 55130 |
| rs71523593 | in-del | -/AC | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27979469 | CACACACACACACAC[-/AC]ACAGAGTTAAATGAA | 55130 |
| rs71978932 | in-del | -/TGAA | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27954496 | ATGAATAAACACGAG[-/TGAA]TGAATGAATGAATGA | 55130 |
| rs72020123 | in-del | -/ATTATT | | | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27960314 | TTATTTATTTATTTC[-/ATTATT]ATTATTATTATTATT | 55130 |
| rs72095120 | in-del | -/T/TT | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27820778 | TGAAGCCCAGCAACT[-/T/TT]TTTTTTTTTTTTTTT | 55130 |
| rs72241269 | in-del | -/A | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27819575 | GAGACCCTGTCTCTT[-/A]AAAAAAAAAAAAAAA | 55130 |
| rs72631844 | snp | A/G | 0.149665 | 0.228982 | intron-variant | ARMC4 | GRCh38.p7 | 10:27828958 | CCTTTATATGTATCT[A/G]TCTTCCAAAATGGGC | 55130 |
| rs72631845 | snp | G/T | 0.138546 | 0.223781 | intron-variant | ARMC4 | GRCh38.p7 | 10:27829176 | TGATTTTGGTTCAGC[G/T]TTCAAAAGCAGATTA | 55130 |
| rs72631846 | snp | C/T | 0.110519 | 0.207473 | intron-variant | ARMC4 | GRCh38.p7 | 10:27831549 | GAGATGAGGAAACCA[C/T]GGCATAGAAAGATTA | 55130 |
| rs72799636 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | ARMC4 | GRCh38.p7 | 10:27814924 | TGGATTCTCATTCAC[C/T]GCCCAGCAATCAAAA | 55130 |
| rs72799641 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27834079 | CAGCTTGGACATCCC[C/G]GTGTGTCACTGACAA | 55130 |
| rs72799642 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | ARMC4 | GRCh38.p7 | 10:27835070 | GTACTTGTAGACATC[A/G]CGTGGCCCTGCGTCC | 55130 |
| rs72799643 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ARMC4 | GRCh38.p7 | 10:27837220 | TGTGACCACATGGTC[C/T]CGTACTGGTCACTCA | 55130 |
| rs72799649 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27863455 | TCAAATTTTTCACTT[A/C]TCTGTGCATGTCCAA | 55130 |
| rs72799676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27940871 | TAAGGCATTCTTCAA[C/T]AGCTACAGTGTTCCT | 55130 |
| rs72799680 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27949031 | AATATTTGAAATAAG[C/G]AAGTATTACCCTGTT | 55130 |
| rs72799682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27949965 | TCATCATTTGAAGTT[A/G]TTATCAGAGCCCCAC | 55130 |
| rs72799693 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27965510 | ATTCATTTGGGCTAT[C/T]GCAGAGCAAGATACG | 55130 |
| rs72799695 | snp | A/C | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27965524 | TTGCAGAGCAAGATA[A/C]GGAGGAGAGTCCAGG | 55130 |
| rs72801808 | snp | C/T | 0.484771 | 0.0859212 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:28000917 | TTGTTTTTTTTTTTT[C/T]TTTTTTTTTTTTTTG | 55130 |
| rs73604078 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ARMC4 | GRCh38.p7 | 10:27821881 | TCTTTTTAATCCTCC[A/G]CCTCCCCTAAAACAC | 55130 |
| rs73604079 | snp | A/G | 0.0663309 | 0.169604 | intron-variant | ARMC4 | GRCh38.p7 | 10:27826901 | CACTCTCCAGCTACC[A/G]CTTTCCAGCTAACAT | 55130 |
| rs73604080 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | ARMC4 | GRCh38.p7 | 10:27830415 | GATACTTGGAAGAAC[A/G]CAGTTTAAACACATG | 55130 |
| rs73604081 | snp | A/G | 0.101301 | 0.200969 | intron-variant | ARMC4 | GRCh38.p7 | 10:27832884 | GCTACTGAGAAAATT[A/G]TCCGACTTATCATGA | 55130 |
| rs73604082 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | ARMC4 | GRCh38.p7 | 10:27833527 | GGCTTATGTGGCTAC[A/G]TAGAAGAAAAATATT | 55130 |
| rs73604083 | snp | C/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27834844 | TGCATGCAGAACACA[C/T]CTAAGTCATAGAGTC | 55130 |
| rs73604084 | snp | A/G | 0.030665 | 0.119967 | intron-variant | ARMC4 | GRCh38.p7 | 10:27842844 | ACTAAAGCTAATTAT[A/G]CATATACCCTTTGAT | 55130 |
| rs73604085 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27843863 | TTTTTCAAAAAATCA[C/T]AAAGAATCTGGTTTA | 55130 |
| rs73604086 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | ARMC4 | GRCh38.p7 | 10:27862106 | GCATGAAGAACCATC[A/G]AGAATCATAACCATG | 55130 |
| rs73604087 | snp | C/T | 0.030278 | 0.119257 | intron-variant | ARMC4 | GRCh38.p7 | 10:27865867 | TCTGTAACACGTTGC[C/T]TTACCTGATTGCTGA | 55130 |
| rs73604088 | snp | A/G/T | 0.0494327 | 0.149241 | intron-variant | ARMC4 | GRCh38.p7 | 10:27869334 | AAATCTCTACAATAG[A/G/T]GCACATTTTAAAATC | 55130 |
| rs73604089 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | ARMC4 | GRCh38.p7 | 10:27869648 | CAAATGATTCTCCTG[A/G]CTTAGCCTCCCAGGT | 55130 |
| rs73604090 | snp | A/C | 0.0498117 | 0.149749 | intron-variant | ARMC4 | GRCh38.p7 | 10:27869834 | GCCACCATGCCTGGC[A/C]GACCAAGTCACTTCT | 55130 |
| rs73604091 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | ARMC4 | GRCh38.p7 | 10:27877768 | ATGCACAATTCAAAT[A/G]TTCATCTGTAATGGC | 55130 |
| rs73604092 | snp | A/T | 0.0295035 | 0.117819 | intron-variant | ARMC4 | GRCh38.p7 | 10:27881475 | GCTTCTACAAAAAAA[A/T]AAAAATTAAAAATTA | 55130 |
| rs73604093 | snp | A/G | 0.030278 | 0.119257 | intron-variant | ARMC4 | GRCh38.p7 | 10:27884821 | CATGTATATGGGGGA[A/G]AAAAATTAAAAGCAT | 55130 |
| rs73604094 | snp | C/G | 0.0298908 | 0.118541 | intron-variant | ARMC4 | GRCh38.p7 | 10:27888128 | GTGATAAACATACAA[C/G]TACATGTATCTTTTT | 55130 |
| rs73604095 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | ARMC4 | GRCh38.p7 | 10:27888371 | GCCATCCTGAATGGA[A/G]TAAGATGATATCTCA | 55130 |
| rs73604096 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27889387 | AGCCACACTTTGATG[C/G]ACACAGCATATCAAA | 55130 |
| rs73604097 | snp | A/C | 0.218151 | 0.247963 | intron-variant | ARMC4 | GRCh38.p7 | 10:27900715 | AAGAAAGGTTATCAG[A/C]TATTGAAGGTCATCT | 55130 |
| rs73604100 | snp | C/T | 0.040671 | 0.13668 | intron-variant | ARMC4 | GRCh38.p7 | 10:27921415 | AAGTAATGGAAAATT[C/T]AGAGCATTAGACTTT | 55130 |
| rs73604101 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27921431 | AGAGCATTAGACTTT[C/T]AGTATGTTTTGAATC | 55130 |
| rs73604102 | snp | A/G | 0.332799 | 0.23589 | intron-variant | ARMC4 | GRCh38.p7 | 10:27921584 | AACTCATATATCTAT[A/G]TGCATATATAAATGG | 55130 |
| rs73606003 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27927655 | CTTATCTTACCAGGC[C/T]TTGCTATAGAATTTA | 55130 |
| rs73606004 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27928264 | ACCGAACATCATCTA[C/T]GACTCCTCCCTATTC | 55130 |
| rs73606005 | snp | A/T | 0.33303 | 0.235809 | intron-variant | ARMC4 | GRCh38.p7 | 10:27931446 | TTTACTGCCTTCTCA[A/T]CATCTACTTTACTAT | 55130 |
| rs73606006 | snp | A/C | 0.141596 | 0.225274 | intron-variant | ARMC4 | GRCh38.p7 | 10:27931508 | CCAGCTCAATCAGGT[A/C]CTTCAGGCTTGTTGT | 55130 |
| rs73606007 | snp | C/T | 0.323671 | 0.238899 | intron-variant | ARMC4 | GRCh38.p7 | 10:27931825 | TAGAAGTAGAGGCTT[C/T]GCAAGAGTAAGTTCT | 55130 |
| rs73606008 | snp | C/G | 0.333261 | 0.235728 | intron-variant | ARMC4 | GRCh38.p7 | 10:27932000 | CACCTTAAATACACT[C/G]AGAACATTACTGCAG | 55130 |
| rs73606009 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27935665 | TATTTGGGTTTAATA[C/G]GTCTCTTGAAATGAG | 55130 |
| rs73606010 | snp | C/G | 0.0283406 | 0.115616 | intron-variant | ARMC4 | GRCh38.p7 | 10:27935683 | CTCTTGAAATGAGTA[C/G]TAGCTTGTGCTACTT | 55130 |
| rs73606011 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27939790 | AATAAATAAATAAAA[C/T]GCAGATTCCTGAGTC | 55130 |
| rs73606012 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27942747 | AATTGTACAATGATT[A/G]CACACAAACCTCCCT | 55130 |
| rs73606013 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27950917 | TAATTAAAAAATAGT[C/T]CAATAAAGTGGACAC | 55130 |
| rs73606015 | snp | A/T | 0.192088 | 0.2432 | intron-variant | ARMC4 | GRCh38.p7 | 10:27952399 | TTTTTATTTTATTTT[A/T]TTTTTTTACCTTAAG | 55130 |
| rs73606016 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27953684 | AGCAAAATGTAGAAT[A/G]AGAAATAGTAGGATT | 55130 |
| rs73606017 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27954622 | TGCTAGCTAGTGGTC[A/G]CATAAACTGTTATGA | 55130 |
| rs73606018 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | ARMC4 | GRCh38.p7 | 10:27954766 | CCCTTTGGGAAAGAC[A/G]GAGAGGAGCCTCTCC | 55130 |
| rs73606019 | snp | A/C | 0.127944 | 0.218179 | intron-variant | ARMC4 | GRCh38.p7 | 10:27956134 | GCTACCCCTCACCAA[A/C]CCATCATGGGTCAGG | 55130 |
| rs73606020 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27957143 | TTGGCCAGAGGAAAA[A/G]ATAATATCCATATAA | 55130 |
| rs73606022 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27958064 | TATAAAATATTTATC[G/T]GTGTCAAAAACCTTG | 55130 |
| rs73606023 | snp | C/T | 0.286564 | 0.247312 | intron-variant | ARMC4 | GRCh38.p7 | 10:27971760 | GAAAAGAGAGTAATA[C/T]CTTTAAAGCACTAAA | 55130 |
| rs73606024 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARMC4 | GRCh38.p7 | 10:27977182 | CTGGGTTTGGAAAAG[C/G]GTTATAAAACACTAT | 55130 |
| rs73606025 | snp | A/C | 0.287606 | 0.247155 | intron-variant | ARMC4 | GRCh38.p7 | 10:27981289 | ATTAATGCCATTGAA[A/C]CCTGAACAATGATAC | 55130 |
| rs73606026 | snp | A/T | 0.418653 | 0.184544 | intron-variant, utr-variant-5-prime | ARMC4 | GRCh38.p7 | 10:27996172 | CTTGTTTCTTTTCTC[A/T]TTTGTATAGCACTTA | 55130 |
| rs73606027 | snp | A/G | 0.081446 | 0.184634 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999566 | CTCTTTTTTTAAATG[A/G]CCTTTACCTTTGTCC | 55130 |
| rs73606028 | snp | A/C | 0.0850919 | 0.187897 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:28000782 | ACCGGATATTTTCCA[A/C]GCAAAAATAACTTAA | 55130 |
| rs73606029 | snp | A/C | 0.0818113 | 0.184966 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:28000879 | ACCTGGGCCCAGTCA[A/C]TCCCTGAAGGATTTA | 55130 |
| rs74127110 | snp | G/T | 0.0166325 | 0.0896639 | intron-variant | ARMC4 | GRCh38.p7 | 10:27825290 | CCAAGTTCTCAATAC[G/T]CAAAAAGATCTGGAG | 55130 |
| rs74127112 | snp | A/C | 0.0763149 | 0.179815 | intron-variant | ARMC4 | GRCh38.p7 | 10:27829461 | CAAGTGTATCTTCAG[A/C]GTCTGTCTTGTCATT | 55130 |
| rs74127119 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | ARMC4 | GRCh38.p7 | 10:27833969 | AGGACAGCGGTGAAG[A/G]TTCCACATGGCGCCA | 55130 |
| rs74127120 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ARMC4 | GRCh38.p7 | 10:27834052 | GTGACATCCAGGCCC[C/T]GCTCTGCTCTCCAGC | 55130 |
| rs74127123 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ARMC4 | GRCh38.p7 | 10:27838889 | GGGACATAGCTACTG[C/T]TGAACAGATCCAAGG | 55130 |
| rs74127131 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | ARMC4 | GRCh38.p7 | 10:27851619 | AAGACAAAGAAAAAA[A/T]TCCTAATTTAAAACA | 55130 |
| rs74127132 | snp | G/T | 0.0433465 | 0.140692 | intron-variant | ARMC4 | GRCh38.p7 | 10:27852124 | AGTCTTTTTTAGATA[G/T]ATAAGACCTGAACGA | 55130 |
| rs74127133 | snp | A/C | 0.121717 | 0.214577 | intron-variant | ARMC4 | GRCh38.p7 | 10:27867000 | TTTTTCTCAAGAAAA[A/C]CGGGAGGAATTCTGG | 55130 |
| rs74127134 | snp | G/T | 0.0640965 | 0.167152 | intron-variant | ARMC4 | GRCh38.p7 | 10:27867404 | AAACTACAAACTGAA[G/T]CCTTTTCTGGGACAA | 55130 |
| rs74127135 | snp | A/C | 0.0640965 | 0.167152 | intron-variant | ARMC4 | GRCh38.p7 | 10:27869027 | AGCAATGAATGAAAA[A/C]CCTAAATTAGAATTG | 55130 |
| rs74127138 | snp | C/T | 0.0916144 | 0.193427 | intron-variant | ARMC4 | GRCh38.p7 | 10:27884002 | GAGAAGAGAAAGAGG[C/T]AGAAAGGATATTTGA | 55130 |
| rs74127139 | snp | A/G | 0.0640965 | 0.167152 | intron-variant | ARMC4 | GRCh38.p7 | 10:27888853 | CAAATGGTGTTGGAT[A/G]TTCACATGCAAAAGA | 55130 |
| rs74127142 | snp | G/T | 0.0726307 | 0.176182 | intron-variant | ARMC4 | GRCh38.p7 | 10:27891385 | AGTTTTTTGTTTTTT[G/T]TTTTTCCTTCAAGAT | 55130 |
| rs74127147 | snp | C/T | 0.0919752 | 0.193722 | intron-variant | ARMC4 | GRCh38.p7 | 10:27907540 | GGCATAAACATTGTG[C/T]AACCCTCTCCCACCA | 55130 |
| rs74127149 | snp | A/C | 0.0962929 | 0.197165 | intron-variant | ARMC4 | GRCh38.p7 | 10:27912869 | TGGGAAAAACAGATT[A/C]GAAGAGAATTTTACC | 55130 |
| rs74127151 | snp | A/C | 0.140919 | 0.224948 | intron-variant | ARMC4 | GRCh38.p7 | 10:27920286 | CTTATGTATAGTTTA[A/C]AAATTAAAAAAATTT | 55130 |
| rs74127152 | snp | A/T | 0.067446 | 0.170804 | intron-variant | ARMC4 | GRCh38.p7 | 10:27920983 | GTGAAAGAGTCTTTC[A/T]TTACACGATCACATA | 55130 |
| rs74127157 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | ARMC4 | GRCh38.p7 | 10:27936101 | TTTGTGTTAAATGGT[C/T]GGGACGTGAATCTCT | 55130 |
| rs74127158 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | ARMC4 | GRCh38.p7 | 10:27936506 | CATGTCAGCAAGCCT[C/T]TTAGTGCCACTGAGG | 55130 |
| rs74127161 | snp | C/T | 0.00489057 | 0.0492074 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944211 | ACGATGACAACATCA[C/T]GGCTACTCACCAGTT | 55130 |
| rs74127163 | snp | G/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27948804 | TTTTTTTTTTTTTTT[G/T]CAATTGACATTTGGC | 55130 |
| rs74127165 | snp | G/T | 0.0659589 | 0.169201 | intron-variant | ARMC4 | GRCh38.p7 | 10:27956089 | ACGCCAGTGTTTGAT[G/T]AATTTGATGATACAG | 55130 |
| rs74127168 | snp | A/G | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27961481 | TTATTTGAAAGAAAC[A/G]TAAAGTAAACTTGGA | 55130 |
| rs74127170 | snp | G/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27961498 | AAAGTAAACTTGGAA[G/T]CAGCATATACATCTT | 55130 |
| rs74127173 | snp | A/G | 0.0685596 | 0.171987 | intron-variant | ARMC4 | GRCh38.p7 | 10:27988892 | TGAGATGGGGAGACT[A/G]TTCTGGGTATTTGGA | 55130 |
| rs74127175 | snp | C/T | 0.0711525 | 0.174681 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27997333 | ATAAGTGCAAATAGC[C/T]TTATCTTATACAGAA | 55130 |
| rs74347601 | snp | G/T | 0.0429648 | 0.14013 | intron-variant | ARMC4 | GRCh38.p7 | 10:27882237 | AAAGAAAGAAAGAAA[G/T]ATGAACTCTCTGATC | 55130 |
| rs74366229 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27961157 | ATATTAATTTTATTC[C/T]ATGGGTTGAGAAAAT | 55130 |
| rs74367968 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | ARMC4 | GRCh38.p7 | 10:27931867 | AATACAATTCAGTGC[A/C]GACACTCTTCAACTC | 55130 |
| rs74372380 | snp | G/T | 0.0659589 | 0.169201 | intron-variant | ARMC4 | GRCh38.p7 | 10:27937214 | GATTTCTGCAGTGAT[G/T]CAACTCAGAGTCTTG | 55130 |
| rs74399544 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | ARMC4 | GRCh38.p7 | 10:27931463 | ATCTACTTTACTATT[C/T]TAAAATTATCACTTC | 55130 |
| rs74421042 | snp | A/G | 0.0584853 | 0.160693 | intron-variant | ARMC4 | GRCh38.p7 | 10:27920862 | CCAATGTAAAAACTG[A/G]AAAAAAAAAACTATG | 55130 |
| rs74493657 | snp | A/G | 0.143622 | 0.226238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27850732 | TAAAATAATTTAAAA[A/G]TGGAAAAAAACTGTG | 55130 |
| rs74511112 | snp | A/C | 0.0256215 | 0.110247 | intron-variant | ARMC4 | GRCh38.p7 | 10:27842591 | AGAAAATTCAAAAAC[A/C]TATAAATGTCTTTAA | 55130 |
| rs74555138 | snp | A/G | 0.00868129 | 0.0653091 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27860667 | GATGCAGTTATCGGC[A/G]TCTTCTGAGAGTTGG | 55130 |
| rs74615463 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27898836 | AAGGATTTGAGATCT[G/T]TTTAATTTTTTGGCT | 55130 |
| rs74615946 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ARMC4 | GRCh38.p7 | 10:27861453 | GAGTCTACTACACAA[C/T]GCAAAATTACAGATC | 55130 |
| rs74640132 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | ARMC4 | GRCh38.p7 | 10:27831616 | AGGATTTGAACCCAA[A/G]CCCTAGATTCCATGC | 55130 |
| rs74643427 | snp | C/T | 0.0667028 | 0.170006 | intron-variant | ARMC4 | GRCh38.p7 | 10:27924852 | ATAGACCACTTTACA[C/T]AGAAGAACTAGAGAA | 55130 |
| rs74658441 | snp | A/G | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27886278 | AAAGTGAAAAAAAAA[A/G]GCAACATGTCATGTA | 55130 |
| rs74666081 | snp | C/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27895056 | GAAAAAAAAAAAAAA[C/T]TGTTAGCTCTTAATA | 55130 |
| rs74761103 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | ARMC4 | GRCh38.p7 | 10:27877914 | TGAAATTTTTGTTCT[A/G]TAGACACAAAGGCTT | 55130 |
| rs74781348 | snp | C/G | 0.0659589 | 0.169201 | intron-variant | ARMC4 | GRCh38.p7 | 10:27925791 | TATGAACAAGACAAA[C/G]AGGATCCCTATCTCC | 55130 |
| rs74785929 | snp | A/C | 0.0170251 | 0.090679 | intron-variant | ARMC4 | GRCh38.p7 | 10:27867054 | TGAATCTCATTCTCC[A/C]TATGAAAACAGTGCA | 55130 |
| rs74801222 | snp | C/T | 0.0592355 | 0.161582 | intron-variant | ARMC4 | GRCh38.p7 | 10:27914520 | CTTGACATTATTCTA[C/T]GAAAAAGAGCTTTTC | 55130 |
| rs74831843 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | ARMC4 | GRCh38.p7 | 10:27919999 | TCATTCAGATACACT[A/C]CAAACAGAAACAAAA | 55130 |
| rs74840990 | snp | A/T | 0.0333695 | 0.124785 | intron-variant | ARMC4 | GRCh38.p7 | 10:27890346 | CACTCTTGGCTGAGG[A/T]GAATATAATGACATA | 55130 |
| rs74889727 | snp | C/T | 0.021333 | 0.101051 | intron-variant | ARMC4 | GRCh38.p7 | 10:27914932 | AAGAAGTGACAGAGT[C/T]CAATGTCTGTGAAAT | 55130 |
| rs74900046 | snp | C/G | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27902318 | AGCAGTGCATAGAGG[C/G]AAATTTATAGCACTA | 55130 |
| rs74937547 | snp | C/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27940281 | ATATATATATAAATG[C/T]CAGTATATATGTGTG | 55130 |
| rs74943085 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARMC4 | GRCh38.p7 | 10:27977198 | GTTATAAAACACTAT[A/G]AGGAAAAAATAAGTT | 55130 |
| rs74946539 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARMC4 | GRCh38.p7 | 10:27817582 | TAATAAGTGAGAACA[C/T]GCAGTTTTGACTTTC | 55130 |
| rs75072627 | snp | A/G | 0.0659589 | 0.169201 | intron-variant | ARMC4 | GRCh38.p7 | 10:27925900 | AAGGAGTAACATTTG[A/G]GAGGCTGAGACAGGA | 55130 |
| rs75143603 | snp | A/C | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872924 | TGGAATAGTTTCAGA[A/C]GGAATGGTACCCGTT | 55130 |
| rs75154112 | snp | C/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27922152 | GAGTGAAACTCTGCC[C/T]CAAAAAAAAAAAAAA | 55130 |
| rs75175828 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27879162 | AAATATCACAGATAA[C/G]TGTGATTTTTCCATT | 55130 |
| rs75189290 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | ARMC4 | GRCh38.p7 | 10:27923699 | ACACCTGTAATCTCA[A/G]TGCTTTGAGAAGCCA | 55130 |
| rs75205738 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | ARMC4 | GRCh38.p7 | 10:27840919 | GTCGAGCTAAAGCTT[C/T]CCAGTCTTTAAAATG | 55130 |
| rs75211000 | snp | A/C | 0.0325976 | 0.123435 | intron-variant | ARMC4 | GRCh38.p7 | 10:27879324 | TTGGAAGAACTTTAT[A/C]ACAAGTATAAGGTGC | 55130 |
| rs75323201 | snp | A/G | 0.116138 | 0.211142 | intron-variant | ARMC4 | GRCh38.p7 | 10:27880480 | ACTTCCTAAGTTCAA[A/G]TGCTATGGTTTGAAT | 55130 |
| rs75357022 | snp | G/T | 0.0165278 | 0.0893908 | intron-variant | ARMC4 | GRCh38.p7 | 10:27908438 | CCACCATCTGTCTTC[G/T]GTTTATATATCAATC | 55130 |
| rs75359486 | snp | C/T | 0.138207 | 0.223612 | intron-variant | ARMC4 | GRCh38.p7 | 10:27928673 | TTGATATAAGAGAAA[C/T]ACAATCAAGAGGCAA | 55130 |
| rs75361717 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | ARMC4 | GRCh38.p7 | 10:27861645 | GAGTGCAGCAAATCC[A/G]AAGACACATTTTGGG | 55130 |
| rs75394736 | snp | A/G | 0.167158 | 0.235875 | intron-variant | ARMC4 | GRCh38.p7 | 10:27923004 | ATGAGGACACTGGAA[A/G]AATTTATAGGTACAA | 55130 |
| rs75470219 | snp | G/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27923185 | TGAATGTGAATGCGT[G/T]TAACTCATTAAAACA | 55130 |
| rs75562851 | snp | C/T | 0.0659589 | 0.169201 | intron-variant | ARMC4 | GRCh38.p7 | 10:27939842 | ACATGGTTAGAAAAC[C/T]ACCTTAAACTATGTG | 55130 |
| rs75593214 | snp | A/G | 0.233235 | 0.249437 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27959595 | AGTGCAGGAGCATGT[A/G]GCCTGAATCTAGCCC | 55130 |
| rs75619684 | snp | A/G | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27902263 | TTGAAACCAATGAGA[A/G]CAAAGACACAGCGTA | 55130 |
| rs75676308 | snp | A/G/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27872991 | TTACCAACCAAAAAG[A/G/T]GTCCAGGACCAGATG | 55130 |
| rs75685482 | snp | A/G | 0.143622 | 0.226238 | intron-variant | ARMC4 | GRCh38.p7 | 10:27849707 | TTAATTCCTACTGAA[A/G]ATAATCTGATTTTGC | 55130 |
| rs75700219 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARMC4 | GRCh38.p7 | 10:27829384 | CTTTTTTCAAACTCC[C/T]GTTGACTTAACCTCA | 55130 |
| rs75715008 | snp | A/C | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27881468 | GACTTCTGCTTCTAC[A/C]AAAAAAAAAAAATTA | 55130 |
| rs75729500 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | ARMC4 | GRCh38.p7 | 10:27934271 | GAAAATGGACTAATA[C/T]GCTTACCTCCCCACA | 55130 |
| rs75758420 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | ARMC4 | GRCh38.p7 | 10:27861654 | AAATCCGAAGACACA[A/T]TTTGGGTCTTCCATT | 55130 |
| rs75763988 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | ARMC4 | GRCh38.p7 | 10:27927484 | GCCATGCCTGAAACA[C/T]AATGCAAAGAGTAAT | 55130 |
| rs75772038 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARMC4 | GRCh38.p7 | 10:27851943 | AACGCAAAAAGATAC[A/G]TGACATACAGAGGAA | 55130 |
| rs75800332 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | ARMC4 | GRCh38.p7 | 10:27897682 | ATTCTTCAAATGTTC[A/G]TGTTGCCGCAATGAT | 55130 |
| rs75849770 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARMC4 | GRCh38.p7 | 10:27925799 | AGACAAAGAGGATCC[C/T]TATCTCCACTACTAT | 55130 |
| rs75851537 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27951734 | GAAACAAAACCTATA[A/T]GCCATGAAGAAATAG | 55130 |
| rs75852285 | snp | G/T | 0.0667028 | 0.170006 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27960062 | ATGCCACAAAAATAT[G/T]TAATATTTATAAAGT | 55130 |
| rs75858925 | snp | A/G | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27850465 | AAAAAAAAAAAAAAA[A/G]AGAATCACTTGAACG | 55130 |
| rs75886239 | snp | A/T | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27961159 | ATTAATTTTATTCTA[A/T]GGGTTGAGAAAATTA | 55130 |
| rs75986449 | snp | G/T | 0.0295035 | 0.117819 | intron-variant | ARMC4 | GRCh38.p7 | 10:27824495 | TTGACAGATGCTGGT[G/T]CCATGCTCTTGAACT | 55130 |
| rs76030084 | snp | C/T | 0.0157012 | 0.0872013 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944459 | AAAAAAGATGAGTGG[C/T]GAATATGTAACCCGT | 55130 |
| rs76116992 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | ARMC4 | GRCh38.p7 | 10:27897156 | CTGGTTTTCCCATCC[A/C]CTTCCCACCCGCCTG | 55130 |
| rs76142618 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | ARMC4 | GRCh38.p7 | 10:27945395 | AGAGAAAAGGAAAAC[A/G]TGCAGGAAGCAGCAC | 55130 |
| rs76179850 | snp | C/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27938613 | TTTTTTCTTTTTTTT[C/T]TCTCTTCTGAGACAG | 55130 |
| rs76200471 | snp | A/G | 0.067446 | 0.170804 | intron-variant | ARMC4 | GRCh38.p7 | 10:27944143 | TATGGAATTTCCAGC[A/G]TGGCCAGAAAGGACA | 55130 |
| rs76266519 | snp | C/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27999118 | TGCTGCTTTCCGCTC[C/G]GCCCCTCCCGGGAAA | 55130 |
| rs76320448 | snp | C/T | 1.65091e-05 | 0.00287303 | synonymous-codon | ARMC4 | GRCh38.p7 | 10:27862545 | TACACTTGCCAGAAC[C/T]TCTTTGTTATCTGAT | 55130 |
| rs76330689 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | ARMC4 | GRCh38.p7 | 10:27824898 | CAAGCTGGATTTTAC[C/T]GAGATTTCCCCAGAA | 55130 |
| rs76352417 | snp | C/T | 0.127944 | 0.218179 | intron-variant | ARMC4 | GRCh38.p7 | 10:27897398 | CAGACGATGTTATTC[C/T]CATGTTTGGTAAAAA | 55130 |
| rs76359107 | snp | C/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27858654 | AACTGTGTGGGTGGG[C/G]CAAACACAGTTTGGT | 55130 |
| rs76360187 | snp | G/T | 0.0410537 | 0.137264 | intron-variant | ARMC4 | GRCh38.p7 | 10:27815815 | CATATGGAACCATCT[G/T]CTAAATTTCTATCTC | 55130 |
| rs76407162 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant, upstream-variant-2KB | ARMC4 | GRCh38.p7 | 10:27983791 | CTTGAGACATCTACA[A/G]CTAACAATCAAAGTC | 55130 |
| rs76429354 | snp | G/T | 0.0322114 | 0.122752 | intron-variant | ARMC4 | GRCh38.p7 | 10:27861508 | ATTTATAGAATATTA[G/T]ATATCCTTAAAGGGA | 55130 |
| rs76452377 | snp | C/T | 0.5 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27969685 | CCAAAACACAATGAC[C/T]CTGTGATTCCCAGAA | 55130 |
| rs76494807 | snp | A/T | 0.0283406 | 0.115616 | intron-variant | ARMC4 | GRCh38.p7 | 10:27954828 | TAAAACACGACAAAT[A/T]CTTTTGTGGGCAATA | 55130 |
| rs76496077 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | ARMC4 | GRCh38.p7 | 10:27898164 | CATTTAAATATAGAT[A/T]TTCAATGACCATTGA | 55130 |
| rs76502818 | snp | A/T | 0.0648419 | 0.167978 | intron-variant | ARMC4 | GRCh38.p7 | 10:27922404 | TTATATAAGTAAATA[A/T]ATATGTAACTGTTGA | 55130 |
| rs76563345 | snp | C/G | 0 | 0 | intron-variant | ARMC4 | GRCh38.p7 | 10:27900791 | AAGAAATGAACAAAG[C/G]CTCCAAGAAATATGG | 55130 |
| rs76576156 | snp | A/G | | | intron-variant | ARMC4 | GRCh38.p7 | 10:27951429 | TTAATGCAAAGAGAA[A/G]ATCCAGAAACAAACT | 55130 |