SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs4924 | snp | A/G | 0.496014 | 0.044466 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362574 | ACTCCTGCCTCATGC[A/G]TACGTCCCACAAATG | 267 |
rs13468 | snp | C/T | 0 | 0 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362192 | GTGTGCCCCATGGGT[C/T]CCCTCCCCTCTCAGC | 267 |
rs731118 | snp | C/G | 0.04543 | 0.143705 | intron-variant | AMFR | GRCh38.p7 | 16:56364207 | ACGGCTGTTCTGGAC[C/G]CAAAGAGAAGGCTGC | 267 |
rs731119 | snp | A/G | 0.367297 | 0.220775 | intron-variant | AMFR | GRCh38.p7 | 16:56364459 | TGAGTTTACATCCTG[A/G]GAATTTTCTGTTCAC | 267 |
rs899242 | snp | C/G | 0.476833 | 0.105105 | intron-variant | AMFR | GRCh38.p7 | 16:56364673 | CCCTGAGCCTGGGGA[C/G]GTTGAGGCTGTGGTG | 267 |
rs1050876 | snp | C/T | 0 | 0 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362214 | CTGGTGCTCCTGCAT[C/T]TCATGAGTGTGCCCC | 267 |
rs1050889 | snp | A/G | 0 | 0 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362056 | TTGGTCCTTGAACAA[A/G]ATGTGGGCCTTGCAA | 267 |
rs1382359 | snp | C/T | 0.409891 | 0.192184 | intron-variant | AMFR | GRCh38.p7 | 16:56365602 | TCCAGCGTGTGTGTG[C/T]GTGTGTGTGTATGTA | 267 |
rs1478478 | snp | G/T | 0.420415 | 0.182917 | intron-variant | AMFR | GRCh38.p7 | 16:56368619 | CTGTCTGAGGTGGTG[G/T]TTTTGATTTTTGAAA | 267 |
rs1593120 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | AMFR | GRCh38.p7 | 16:56377910 | taagttctatatgag[A/G]aaaattacaaaatct | 267 |
rs1804879 | snp | A/G | 0.000268678 | 0.0115874 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362163 | GCATTTCCTTGTCCC[A/G]TCTGGACCTGGGGAG | 267 |
rs1804880 | snp | C/T | | | synonymous-codon | AMFR | GRCh38.p7 | 16:56363011 | TGCGGCCTCAGAGAG[C/T]TTCCTCCCCTCGGAA | 267 |
rs2219776 | snp | C/G | 0.420255 | 0.183066 | intron-variant | AMFR | GRCh38.p7 | 16:56365377 | TAGGTTGGTTCCCTC[C/G]TGCAGGAGCCCTATC | 267 |
rs2241956 | snp | C/T | 0.420255 | 0.183066 | intron-variant | AMFR | GRCh38.p7 | 16:56366935 | CTCAAGAAAGCCATG[C/T]TTTCCCCCCAGCCCC | 267 |
rs2241957 | snp | C/T | 0.410061 | 0.192043 | intron-variant | AMFR | GRCh38.p7 | 16:56367382 | TGAGGAAGACCACTG[C/T]CGGGACCACATTCCC | 267 |
rs2432536 | snp | A/G | 0.470132 | 0.118498 | intron-variant | AMFR | GRCh38.p7 | 16:56391901 | ggaggcagtctgtcc[A/G]ttctcagatctcaaa | 267 |
rs2432537 | snp | C/T | 0.425277 | 0.178263 | intron-variant | AMFR | GRCh38.p7 | 16:56391419 | TTCCCTGACCCCTTG[C/T]GCTTCCCGGGTGAGG | 267 |
rs2432538 | snp | C/T | 0.420415 | 0.182917 | intron-variant | AMFR | GRCh38.p7 | 16:56387515 | TGCTATTCGCATCCC[C/T]GATTTGAGTTTCAAG | 267 |
rs2432539 | snp | C/T | 0.408017 | 0.193729 | intron-variant | AMFR | GRCh38.p7 | 16:56387075 | GGAGTCTTGCCCTGT[C/T]GCCAGGCTGGAGTGC | 267 |
rs2432540 | snp | C/T | 0.47666 | 0.105476 | intron-variant | AMFR | GRCh38.p7 | 16:56385716 | ATTTTATTTCTGTGG[C/T]GGATAATCTAACCTT | 267 |
rs2432541 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | AMFR | GRCh38.p7 | 16:56383621 | gaagctgccttgctg[A/G]gtttgaattaagcag | 267 |
rs2432542 | snp | A/T | 0.494057 | 0.0541878 | intron-variant | AMFR | GRCh38.p7 | 16:56403960 | ATCTTCTTTTTTTAA[A/T]TTTTTTTTCCTCATG | 267 |
rs2440466 | snp | A/G | 0.4231 | 0.180378 | intron-variant | AMFR | GRCh38.p7 | 16:56377253 | atcaaatccaacaac[A/G]cataaaaataattat | 267 |
rs2440467 | snp | C/T | 0.410061 | 0.192043 | intron-variant | AMFR | GRCh38.p7 | 16:56383135 | CATTTCAATCTACCA[C/T]AATCTACTGTCCAAC | 267 |
rs2440468 | snp | A/G | 0.481009 | 0.0955756 | intron-variant | AMFR | GRCh38.p7 | 16:56386682 | CTTCTGTTATTTCCC[A/G]AAGAAAACAGGAGCC | 267 |
rs2440469 | snp | G/T | 0.0221141 | 0.102801 | intron-variant | AMFR | GRCh38.p7 | 16:56387001 | acttgggaggctgag[G/T]caggagaatcacttg | 267 |
rs2440470 | snp | G/T | 0.403158 | 0.197592 | intron-variant | AMFR | GRCh38.p7 | 16:56387039 | GAATCAGCGGTTGCA[G/T]TGAGTTGAGATCACG | 267 |
rs2440471 | snp | A/T | 0.0221141 | 0.102801 | intron-variant | AMFR | GRCh38.p7 | 16:56388196 | ctacacacctaggct[A/T]tacgatatagtctat | 267 |
rs2440472 | snp | C/T | 0.473266 | 0.112482 | intron-variant | AMFR | GRCh38.p7 | 16:56402912 | GCAGATCCCAGAGTA[C/T]GTCAGAATGTATGTT | 267 |
rs2440473 | snp | C/T | 0.425277 | 0.178263 | intron-variant | AMFR | GRCh38.p7 | 16:56399622 | tcacctggcaaccac[C/T]gatccactttctgtc | 267 |
rs2440474 | snp | A/C | 0.42574 | 0.177808 | intron-variant | AMFR | GRCh38.p7 | 16:56398523 | GAAACATGTAGAGat[A/C]tatgtgtataggtgt | 267 |
rs2440475 | snp | C/T | 0.425277 | 0.178263 | intron-variant | AMFR | GRCh38.p7 | 16:56391507 | cccaccctaatactg[C/T]gcttttccaatggtc | 267 |
rs2440476 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | AMFR | GRCh38.p7 | 16:56391558 | agattatatcctgcg[C/T]gtggctcggagggtc | 267 |
rs2550303 | snp | A/G | 0.420415 | 0.182917 | | | GRCh38.p7 | 16:56361698 | TTTGCCAATAATTGT[A/G]GATAATACTGGATTC | 267 |
rs2550304 | snp | A/T | | | | | GRCh38.p7 | 16:56366182 | aggagatcgagacca[A/T]cctggctaacacagc | 267 |
rs2550305 | snp | A/G | 0.395635 | 0.2032 | | | GRCh38.p7 | 16:56366235 | TACAAAAAATTAGCC[A/G]GGCGTGGTGGTGGGC | 267 |
rs2550306 | snp | A/C | 0.0170251 | 0.090679 | | | GRCh38.p7 | 16:56378367 | atagagaaaagatag[A/C]cttttcaacaaatgg | 267 |
rs2550307 | snp | A/G | 0.410061 | 0.192043 | | | GRCh38.p7 | 16:56380219 | ctgaaggctgccaag[A/G]cttggggcttccacc | 267 |
rs2550308 | snp | C/G | 0.410061 | 0.192043 | | | GRCh38.p7 | 16:56382316 | tatatgaggtaccta[C/G]gtagttaaactcata | 267 |
rs2550309 | snp | A/G | 0.42574 | 0.177808 | | | GRCh38.p7 | 16:56400830 | ATGCCTGGTTCATTC[A/G]CTTTTGACTCCTCCA | 267 |
rs2550310 | snp | C/T | 0.473266 | 0.112482 | | | GRCh38.p7 | 16:56404198 | GCCACCGCGTCCAGC[C/T]GAGGCTCTTTTTTAA | 267 |
rs2587862 | snp | A/T | 0.00159617 | 0.0282053 | | | GRCh38.p7 | 16:56365699 | AGTGAAGAGGCGAGA[A/T]GTTAGAAAGAAAACA | 267 |
rs2587863 | snp | A/C | 0.0221141 | 0.102801 | | | GRCh38.p7 | 16:56367354 | GTGCCCTAAGCCTTG[A/C]AAGCTTCAGGACTGA | 267 |
rs2587864 | snp | G/T | 0.0221141 | 0.102801 | | | GRCh38.p7 | 16:56367822 | GCAGAGAACACTGAC[G/T]GAACACCTAACTTCG | 267 |
rs2587865 | snp | C/T | 0.0170251 | 0.090679 | | | GRCh38.p7 | 16:56368632 | AACCACCACCTCAGA[C/T]AGATGAACGGTAGCT | 267 |
rs2587866 | snp | C/T | 0.410399 | 0.191761 | | | GRCh38.p7 | 16:56369987 | gagtggaatgagaca[C/T]tgtactatgaaaggt | 267 |
rs2587867 | snp | C/T | 0.480775 | 0.0961398 | | | GRCh38.p7 | 16:56370099 | cagacttcaccactg[C/T]gcaatacctgcatgt | 267 |
rs2587868 | snp | G/T | 0.0023933 | 0.0345097 | | | GRCh38.p7 | 16:56371446 | CACCCTTGAAGTCTT[G/T]ACTTTTTAAAGGAGG | 267 |
rs2587869 | snp | A/G | 0.41023 | 0.191902 | | | GRCh38.p7 | 16:56373014 | aacaacaacaacaaa[A/G]AAAACCATGGaggaa | 267 |
rs2587870 | snp | C/T | 0.420255 | 0.183066 | | | GRCh38.p7 | 16:56376919 | TTATACAGATAACTT[C/T]TTATAATTAGAATTG | 267 |
rs2587871 | snp | C/T | 0.420892 | 0.182472 | | | GRCh38.p7 | 16:56378614 | ctggacttcattaaa[C/T]gtaaaaagttctgca | 267 |
rs2587872 | snp | C/T | 0.420096 | 0.183214 | | | GRCh38.p7 | 16:56378784 | aaaatgggtataaga[C/T]cttaatagatacttc | 267 |
rs2587873 | snp | C/G | 0.410061 | 0.192043 | | | GRCh38.p7 | 16:56378822 | atagatgtacagatg[C/G]caaataagaatataa | 267 |
rs2587874 | snp | A/G | 0.480775 | 0.0961398 | | | GRCh38.p7 | 16:56379852 | tccacccctgtggct[A/G]tgcagggtacagcct | 267 |
rs2617845 | snp | C/T | 0.0217236 | 0.101931 | downstream-variant-500B | AMFR | GRCh38.p7 | 16:56361025 | AATAAGCTCCTGCTC[C/T]AAACACTGTGATATG | 267 |
rs2617846 | snp | A/G | 0.476833 | 0.105105 | intron-variant | AMFR | GRCh38.p7 | 16:56363241 | TCTCTGCACCAGGGA[A/G]GAACCCTTCAGTGCT | 267 |
rs2617847 | snp | C/G | 0.410061 | 0.192043 | intron-variant | AMFR | GRCh38.p7 | 16:56363262 | CTTCAGTGCTGTTCC[C/G]TGCTGTCTCTTCCTG | 267 |
rs2617848 | snp | C/T | 0.420255 | 0.183066 | intron-variant | AMFR | GRCh38.p7 | 16:56365923 | AGGTTCCCTGTGAAA[C/T]ACATACTTTCCTCCA | 267 |
rs2617849 | snp | C/T | 0.410399 | 0.191761 | intron-variant | AMFR | GRCh38.p7 | 16:56370791 | ACATATGTAAATTAA[C/T]TCTATAAATGTTTAC | 267 |
rs2617850 | snp | A/G | 0.41023 | 0.191902 | intron-variant | AMFR | GRCh38.p7 | 16:56375887 | aacatgatgaaaccc[A/G]tctctactaaaaata | 267 |
rs2920704 | snp | C/T | 0.474554 | 0.109889 | intron-variant | AMFR | GRCh38.p7 | 16:56407950 | AGGTGAGATACTGGA[C/T]GCAGGACTTGCTCAG | 267 |
rs2920705 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | AMFR | GRCh38.p7 | 16:56407284 | AATTAGTATTATTAA[A/T]TAAAAAATGAGATAT | 267 |
rs2920706 | snp | C/T | 0.402982 | 0.197728 | intron-variant, upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56424575 | CTAACAATCCCATGC[C/T]TGACCAAGTGGGAAA | 267 |
rs2966204 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56424429 | AATCGAATACTAAGC[A/G]GCAAAAAAGTTGTGG | 267 |
rs2966205 | snp | C/T | 0.42574 | 0.177808 | intron-variant | AMFR | GRCh38.p7 | 16:56412700 | TTCCGTCTCTACAAA[C/T]ACCTAAACAATTAGC | 267 |
rs2966206 | snp | C/T | 0.404035 | 0.196909 | intron-variant | AMFR | GRCh38.p7 | 16:56407341 | AATGGCTATATTTGC[C/T]TTTTCTTCAGGCCAA | 267 |
rs3038885 | in-del | -/AAAAAAAAA | | | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56361775 | aaaaaaaaaaaaaaa[-/AAAAAAAAA]GTAATCCAATGGGGC | 267 |
rs3038887 | in-del | -/CA | | | intron-variant | AMFR | GRCh38.p7 | 16:56365544 | ACACACACACACACA[-/CA]GACACACGTAGTTGG | 267 |
rs3748401 | snp | A/C | 0.0382518 | 0.132901 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362518 | CACACTGTGCGCCTC[A/C]CCCACACTCTTCCCA | 267 |
rs3790117 | snp | C/G | 0.111576 | 0.20818 | intron-variant | AMFR | GRCh38.p7 | 16:56363655 | GCTTAGATCAGGTTA[C/G]CACACAAGTGCTCTC | 267 |
rs3996541 | in-del | -/A/AA/AAA | | | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56361534 | AATTAAAAAAAAAAA[-/A/AA/AAA]TCACAGAAATTTACT | 267 |
rs4238787 | snp | C/T | 0.489342 | 0.0722168 | intron-variant | AMFR | GRCh38.p7 | 16:56408154 | CTGCTCATTCTTCTT[C/T]ATGGAAGTGTTAAAC | 267 |
rs4462584 | snp | C/T | 0.414741 | 0.188044 | intron-variant | AMFR | GRCh38.p7 | 16:56409938 | TTTTGGAGGCTGAGG[C/T]GGGTAGACAGCTTGA | 267 |
rs4541073 | snp | C/T | 0.419776 | 0.18351 | intron-variant | AMFR | GRCh38.p7 | 16:56417988 | agcaacatggcaaaa[C/T]cccatctctactaaa | 267 |
rs4620948 | snp | A/G | 0.415563 | 0.18732 | intron-variant | AMFR | GRCh38.p7 | 16:56405864 | ATGGTGGCACGTGCC[A/G]GTAGTCCCAGCTACT | 267 |
rs4783938 | snp | A/G | 0.475525 | 0.107882 | intron-variant | AMFR | GRCh38.p7 | 16:56373111 | gggcactcaggcaga[A/G]gtggctcccctgtaa | 267 |
rs4783940 | snp | C/T | 0.419776 | 0.18351 | intron-variant | AMFR | GRCh38.p7 | 16:56417570 | agcaccaacatggcg[C/T]cacaagtggaaaatt | 267 |
rs4784664 | snp | C/T | 0.479904 | 0.0982045 | intron-variant | AMFR | GRCh38.p7 | 16:56413374 | TAAAAATATATAAAT[C/T]AGCTGTGGTGCACAC | 267 |
rs4784665 | snp | A/G | 0.472709 | 0.11358 | intron-variant | AMFR | GRCh38.p7 | 16:56413440 | CAAGTGCTTGAACCC[A/G]GGAGGCAGAGGTTGC | 267 |
rs4784666 | snp | C/T | 0.482831 | 0.0910472 | intron-variant | AMFR | GRCh38.p7 | 16:56413452 | CCCGGGAGGCAGAGG[C/T]TGCAGTGAGCTGAGA | 267 |
rs5817062 | in-del | -/A | 0.436265 | 0.166749 | intron-variant | AMFR | GRCh38.p7 | 16:56416897 | ACATGGCTAACCAGG[-/A]AAAAAAAAAAAAAAG | 267 |
rs6499834 | snp | C/T | 0.410399 | 0.191761 | intron-variant | AMFR | GRCh38.p7 | 16:56408822 | AACAAGGCCCTGGAG[C/T]GGGTTTAACTGAGGG | 267 |
rs6499835 | snp | A/G | 0 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56408850 | GGGGCAGCACTGTAG[A/G]TGCACATTTATCTGG | 267 |
rs6499836 | snp | C/G | 0.419616 | 0.183658 | intron-variant | AMFR | GRCh38.p7 | 16:56419624 | atggtgaaatcccgt[C/G]tctactaaaaataca | 267 |
rs6499837 | snp | C/T | 0.404559 | 0.196498 | intron-variant | AMFR | GRCh38.p7 | 16:56420069 | ATGGTTCTACTCTTC[C/T]ACTGGAGAAAACAGA | 267 |
rs7184479 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | AMFR | GRCh38.p7 | 16:56368898 | attatctgcctttta[A/T]agaaaaaaatgtggc | 267 |
rs7185879 | snp | C/T | 0.473359 | 0.112298 | intron-variant | AMFR | GRCh38.p7 | 16:56394096 | aaactgaacaacctg[C/T]tcctgaatgactact | 267 |
rs7187883 | snp | A/C | 0.419936 | 0.183362 | intron-variant | AMFR | GRCh38.p7 | 16:56412087 | CTAAGCACTTAAAAA[A/C]GCATCAAAAAGCTTC | 267 |
rs7198867 | snp | A/C | 0.371177 | 0.218669 | intron-variant | AMFR | GRCh38.p7 | 16:56419174 | gattacaggcacctg[A/C]caccatgcctggcta | 267 |
rs7200888 | snp | C/T | 0.381503 | 0.21262 | intron-variant | AMFR | GRCh38.p7 | 16:56422670 | CCAAGCTGGTTCAAA[C/T]ACCACCTTCCATGAA | 267 |
rs7203069 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | AMFR | GRCh38.p7 | 16:56371539 | GCCTGCCATGAGCCC[A/G]GCAGTAGCTGCACTG | 267 |
rs7203090 | snp | C/T | 0.420096 | 0.183214 | intron-variant | AMFR | GRCh38.p7 | 16:56410527 | AATATACCAATATAC[C/T]GTTTCAATGGCTAAA | 267 |
rs7203330 | snp | C/T | 0.476746 | 0.10529 | intron-variant | AMFR | GRCh38.p7 | 16:56410656 | GGTGGCCAGGGCAGG[C/T]GGATCACTTGAGCCC | 267 |
rs7205230 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | AMFR | GRCh38.p7 | 16:56368900 | tatctgccttttaaa[A/G]aaaaaaatgtggcca | 267 |
rs7205852 | snp | A/T | 0.287085 | 0.247234 | intron-variant | AMFR | GRCh38.p7 | 16:56375226 | agtgtattttatgtg[A/T]ggtccaagacaattc | 267 |
rs8043596 | snp | C/T | 0.428635 | 0.174898 | intron-variant | AMFR | GRCh38.p7 | 16:56385391 | ggaggccaaggcgga[C/T]ggatcactaaggcca | 267 |
rs8049318 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | AMFR | GRCh38.p7 | 16:56408582 | TTACCACTACTACAA[C/T]GTGATGTCAGCATTA | 267 |
rs8052353 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56403940 | ttaaatacaaaaaat[A/T]caagcatgaggaaaa | 267 |
rs8054153 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | AMFR | GRCh38.p7 | 16:56379588 | aggcaagtccctaac[A/G]tctatgagcctgtaa | 267 |
rs8055125 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | AMFR | GRCh38.p7 | 16:56379452 | catatcattccgccc[C/T]ggcccctcccaaatc | 267 |
rs8060071 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | AMFR | GRCh38.p7 | 16:56379357 | aaagacctgccccca[C/T]gattcaactacctcc | 267 |
rs9673277 | snp | A/C | 0.425277 | 0.178263 | intron-variant | AMFR | GRCh38.p7 | 16:56395309 | aaccaaatgcagcag[A/C]acatcaaaaacctta | 267 |
rs9673282 | snp | A/C | 0.289165 | 0.246913 | intron-variant | AMFR | GRCh38.p7 | 16:56395440 | aaaccacatgattat[A/C]tcaatagatgcagaa | 267 |
rs9673290 | snp | C/T | 0.473451 | 0.112115 | intron-variant | AMFR | GRCh38.p7 | 16:56395562 | tttatgacaaaccca[C/T]agccaacatcatact | 267 |
rs9708450 | snp | C/T | 0.473451 | 0.112115 | intron-variant | AMFR | GRCh38.p7 | 16:56396659 | caccaaaagcaatgg[C/T]aaccaaagccaaaat | 267 |
rs9745735 | snp | A/G | 0.370974 | 0.218781 | intron-variant | AMFR | GRCh38.p7 | 16:56397008 | accagttagaatggc[A/G]atcattaaaaaggaa | 267 |
rs9921942 | snp | C/G | 0.276534 | 0.248588 | intron-variant | AMFR | GRCh38.p7 | 16:56384424 | AACAGGTTCTCAGTT[C/G]AAATTTGTTCAATCA | 267 |
rs9922336 | snp | C/T | 0.410568 | 0.191619 | intron-variant | AMFR | GRCh38.p7 | 16:56385507 | AGCTACTCAGGAGGC[C/T]GAGGTAAGAGAATTG | 267 |
rs9922982 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | AMFR | GRCh38.p7 | 16:56373105 | attccagggcactca[A/G]gcagaggtggctccc | 267 |
rs9923627 | snp | C/G | 0.425432 | 0.178112 | intron-variant | AMFR | GRCh38.p7 | 16:56396021 | caaactaatgctcaa[C/G]aaaataaaagaggac | 267 |
rs9928602 | snp | C/G | 0.377582 | 0.214995 | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56427416 | CCATAACTTTTAAAC[C/G]ACTGACTGGCAATCT | 267 |
rs9933064 | snp | C/T | 0.175576 | 0.238665 | intron-variant | AMFR | GRCh38.p7 | 16:56371875 | AGGCTTTCTTGTCAT[C/T]ATTCCTAAACAATAC | 267 |
rs9933608 | snp | A/G | 0 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56402697 | AGCCTAATACTGAGC[A/G]CTATCTGCCCAGTAC | 267 |
rs9934081 | snp | A/G | 0.425432 | 0.178112 | intron-variant | AMFR | GRCh38.p7 | 16:56396022 | aaactaatgctcaac[A/G]aaataaaagaggaca | 267 |
rs9939175 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56374405 | ggacaaaggtaaaaa[A/C]aaaaaaaaaaaaaaa | 267 |
rs9939181 | snp | A/C | 0.444444 | 0.157135 | intron-variant | AMFR | GRCh38.p7 | 16:56374415 | aaaaaaaaaaaaaaa[A/C]aaaaaaaacactaca | 267 |
rs10556688 | in-del | -/TCT | | | intron-variant | AMFR | GRCh38.p7 | 16:56367919 | TGCTGTTACCGTCCT[-/TCT]AGCCAGTTTAAGATC | 267 |
rs10646853 | in-del | -/AC | | | intron-variant | AMFR | GRCh38.p7 | 16:56365543 | GTTGGCATAACATGT[-/AC]ACACACACACACACA | 267 |
rs10649127 | in-del | -/A/AA | 0 | 0 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56361523 | TCAGCAAAACAAATT[-/A/AA]AAAAAAAAAAATCAC | 267 |
rs10709501 | in-del | -/T | 0.414741 | 0.188044 | intron-variant | AMFR | GRCh38.p7 | 16:56372345 | TTATTTCATGTAGCA[-/T]TAATGTCCTCCAGGT | 267 |
rs11271968 | in-del | -/GGGGAGGGGAGTC | 0.471292 | 0.116318 | intron-variant | AMFR | GRCh38.p7 | 16:56370015 | GTGGAAAGGTAGGGA[-/GGGGAGGGGAGTC]GGGGAGGGCTGGAAA | 267 |
rs11385813 | in-del | -/A | 0.499977 | 0.00339449 | intron-variant | AMFR | GRCh38.p7 | 16:56412863 | AGAAAAAAAAAAAAA[-/A]GGCAGCATTTACAAC | 267 |
rs11644357 | snp | G/T | 0.473266 | 0.112482 | intron-variant | AMFR | GRCh38.p7 | 16:56411340 | CTCCTGCGCTCAAGC[G/T]ATCCTCCCACCTCAG | 267 |
rs11648595 | snp | A/C | 0 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56374295 | aaaagagaaacgaac[A/C]caagaaatatttgaa | 267 |
rs11860803 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56394472 | ctgctggccgggcgc[A/G]gtggctcacgcctgt | 267 |
rs11860832 | snp | A/G | 0.415563 | 0.18732 | intron-variant | AMFR | GRCh38.p7 | 16:56394515 | ttgggaggccgaggc[A/G]ggtggatcatgaggt | 267 |
rs11862373 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | AMFR | GRCh38.p7 | 16:56392758 | gtacctgaaagtgac[A/G]gggagaatggaatca | 267 |
rs11862375 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | AMFR | GRCh38.p7 | 16:56392782 | ggaatcaagttggaa[A/G]acactctgcaggata | 267 |
rs11864417 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | AMFR | GRCh38.p7 | 16:56382219 | aaattctgacttgtg[C/G]tacaacgtggatgaa | 267 |
rs12102661 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56409671 | AACAAAAGCCGGCTT[C/T]TATGGAAGATATATT | 267 |
rs12103241 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56409724 | TGTCCTCaagaaaac[A/G]gaaaaaaaaaaaaaa | 267 |
rs12149221 | snp | A/T | 0 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56369611 | AGAATATTCCAGTTT[A/T]AAAAAGTGTTCATTT | 267 |
rs12325384 | snp | G/T | 0.210605 | 0.246877 | intron-variant | AMFR | GRCh38.p7 | 16:56420199 | TTGGCCACCAACAGG[G/T]GCTTATTTATGACCT | 267 |
rs12444041 | snp | A/G | 0.298905 | 0.24517 | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56426131 | TGACCATTTGACCCA[A/G]TAATTCCACTCCTCT | 267 |
rs12444088 | snp | C/T | 0.247905 | 0.249991 | intron-variant | AMFR | GRCh38.p7 | 16:56380430 | agatattttccccat[C/T]gtcttggggattaac | 267 |
rs12445699 | snp | A/G | 0.415563 | 0.18732 | intron-variant | AMFR | GRCh38.p7 | 16:56418672 | aaattatccgggcac[A/G]tggtgggcgcctgta | 267 |
rs12597607 | snp | A/G | 0.461037 | 0.134028 | intron-variant | AMFR | GRCh38.p7 | 16:56398284 | gtatcatttatatat[A/G]taaatgtatcattta | 267 |
rs12597683 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56405184 | AGGCCTCCATCACCT[C/T]CCTCCCCAATTTCAC | 267 |
rs12597761 | snp | A/C | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56398267 | catttatatatgtaa[A/C]tgtatcatttatata | 267 |
rs12599466 | snp | C/T | 0.444444 | 0.157135 | intron-variant | AMFR | GRCh38.p7 | 16:56391265 | taggaacagctccag[C/T]ctacagctcccagca | 267 |
rs12922835 | snp | C/G/T | 0.00358779 | 0.0422022 | intron-variant | AMFR | GRCh38.p7 | 16:56369411 | GTCTGGCAGGCTTTG[C/G/T]GCAGTGAATGTGGCA | 267 |
rs12925932 | snp | A/C | | | intron-variant, upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56425043 | CAGCGGAccccgccc[A/C]tgccccgcgggcccg | 267 |
rs12927560 | snp | G/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56420718 | CAGCTCTTAAttttg[G/T]tttgttttttttttt | 267 |
rs12928169 | snp | A/C | 0 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56383001 | TGACCTATTCAAAAA[A/C]CTTAAACAAACGAAA | 267 |
rs12928170 | snp | A/C/T | 0 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56383002 | GACCTATTCAAAAAC[A/C/T]TTAAACAAACGAAAA | 267 |
rs12928709 | snp | A/G | 0 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56383019 | TAAACAAACGAAAAC[A/G]CTTCCCTGGATGCTA | 267 |
rs12930191 | snp | A/G | 0 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56418952 | TTGCCATTTCTGGAA[A/G]AGAGAAGCAGGTAAC | 267 |
rs12931750 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | AMFR | GRCh38.p7 | 16:56404744 | TGGCACTGCCTTACA[C/T]CCAGTGGCAAAAAGA | 267 |
rs12932470 | snp | A/T | 0 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56383084 | TCCTTCTTCATAACA[A/T]ACTTCCTGGTATGGT | 267 |
rs12934488 | snp | A/T | 0 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56377276 | ataattataaactac[A/T]tccaagtggtattta | 267 |
rs13330457 | snp | A/T | 0.25634 | 0.24992 | intron-variant | AMFR | GRCh38.p7 | 16:56423421 | TCCTAAAAAGTAATC[A/T]TCATCACAGAAAAAT | 267 |
rs13331718 | snp | C/T | 0.248471 | 0.249995 | intron-variant, utr-variant-5-prime | AMFR | GRCh38.p7 | 16:56423792 | TAGATAAACAGGAAC[C/T]TCACCCTTCACTGCC | 267 |
rs13333817 | snp | G/T | 0.0356815 | 0.128715 | intron-variant | AMFR | GRCh38.p7 | 16:56385511 | actcaggaggctgag[G/T]taagagaattgcttg | 267 |
rs13338179 | snp | A/G | 0 | 0 | missense | AMFR | GRCh38.p7 | 16:56409584 | CAAAATTTGTCTTTG[A/G]GATGCTAAAAAAGAA | 267 |
rs17355357 | snp | C/T | 0.255782 | 0.249933 | intron-variant | AMFR | GRCh38.p7 | 16:56367064 | CGGCTCCCTGGAGAG[C/T]TTGCCCTAGGCCATC | 267 |
rs28362030 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56418520 | AAAAAAAACAAAAAA[A/C]AAAAAAACGCCAGGC | 267 |
rs28472677 | snp | G/T | 0.252421 | 0.249988 | intron-variant | AMFR | GRCh38.p7 | 16:56383390 | GGCAGAACCTAGAGC[G/T]CAGATGTCAGCCCTC | 267 |
rs28506013 | snp | A/T | 0.00676609 | 0.0577691 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56361467 | TAGAGTTTGCTTTTT[A/T]TTATTATTATTGTTT | 267 |
rs28635619 | snp | A/G | 0.257176 | 0.249897 | intron-variant | AMFR | GRCh38.p7 | 16:56422386 | GAGAAAGAAACCTTC[A/G]AGGGGGTTGCTCACC | 267 |
rs28793026 | snp | C/T | 0.185788 | 0.241613 | intron-variant | AMFR | GRCh38.p7 | 16:56381874 | TCTATCAAACATACC[C/T]TCTGCTGAGGGATGT | 267 |
rs28867774 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56396370 | ACAGAGCCCTCAGAA[A/G]CAATACCACACATCT | 267 |
rs28895877 | snp | G/T | 0.25634 | 0.24992 | intron-variant | AMFR | GRCh38.p7 | 16:56397426 | AGCAAACTATCACAA[G/T]GACAAAAAGACACAC | 267 |
rs34019018 | in-del | -/A | | | intron-variant | AMFR | GRCh38.p7 | 16:56374006 | AACCCTGTCTCTACT[-/A]AAAATACAAAAATTT | 267 |
rs34111267 | in-del | -/A | | | intron-variant | AMFR | GRCh38.p7 | 16:56414535 | AGGGATGAGGACCGG[-/A]AAAGAGAGGCACCAG | 267 |
rs34254898 | in-del | -/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56406918 | AACATAAGTATCATT[-/G]CTAACTTTGCAATAA | 267 |
rs34270592 | snp | A/C | 0.480302 | 0.0972668 | intron-variant | AMFR | GRCh38.p7 | 16:56397766 | ATTTATAATATATAA[A/C]TGTATCATTTATAAT | 267 |
rs34273259 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56397788 | ATTTATAATATATAA[A/C]TGTATCATTTATAAT | 267 |
rs34334917 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56406660 | TTAAATTCCCATTTG[A/T]AAGTGAAAAATATTT | 267 |
rs34530182 | in-del | -/T | 0.487995 | 0.0765403 | intron-variant | AMFR | GRCh38.p7 | 16:56411236 | TGATTCTAAGTATAC[-/T]TTTTTTTTTTTTTTT | 267 |
rs34624114 | in-del | -/A | 0.428182 | 0.17536 | intron-variant | AMFR | GRCh38.p7 | 16:56390896 | TATAGTTTTCTGTTT[-/A]AAAAAAAAAAAAAAT | 267 |
rs34642234 | in-del | -/T/TT | 0.491936 | 0.0629843 | intron-variant | AMFR | GRCh38.p7 | 16:56404037 | TTTTTTTTTTTTTTT[-/T/TT]GGGACGGAGTGTCAC | 267 |
rs34735121 | in-del | -/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56368516 | TTGGGGTAGATTATT[-/C]CCCTGGTCATACACA | 267 |
rs34765371 | in-del | -/A | 0 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56399083 | TTAAGAATTATTACT[-/A]AAAAAAAAAACAAAA | 267 |
rs34826033 | in-del | -/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56408679 | TAAAAAAAACAGTTT[-/G]GGGAGGTTAGAAGCT | 267 |
rs34850483 | in-del | -/AC/CG | 0.236724 | 0.249647 | intron-variant | AMFR | GRCh38.p7 | 16:56365591 | TACATACACACACAC[-/AC/CG]GCACACACACGCTGG | 267 |
rs34911031 | in-del | -/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56397131 | GGCGATTCCTCAGGG[-/T]ATCTAGAACTAGAAA | 267 |
rs34923802 | in-del | -/G | | | intron-variant, frameshift-variant | AMFR | GRCh38.p7 | 16:56388784 | CATCAGTATCACTGT[-/G]CGACCACCTCCACCT | 267 |
rs34939661 | in-del | -/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56365715 | TTAGAAAGAAAACAG[-/C]CCGCCCACCGCAACC | 267 |
rs34940165 | in-del | -/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56405535 | TGACCATCAATTCTA[-/T]TTTCACACAGCATTA | 267 |
rs34940309 | in-del | -/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56367555 | AGTACCAAAAACAGT[-/C]CCAGAGTCACACAGA | 267 |
rs34952840 | in-del | -/C | 0.275999 | 0.248644 | intron-variant | AMFR | GRCh38.p7 | 16:56380334 | GGACCCTGAGCATGA[-/C]CCACGAAACCATGTT | 267 |
rs34954005 | in-del | -/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56413179 | TAGAATAAAACACAA[-/T]TTTTGTTCTTATGTT | 267 |
rs35282564 | snp | C/T | | | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56361648 | TTACTTTTCAACATT[C/T]TAAAAACTTTCCGTT | 267 |
rs35308464 | in-del | -/A | 0.453087 | 0.145793 | intron-variant | AMFR | GRCh38.p7 | 16:56394750 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 267 |
rs35312859 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56375260 | TTCCAATGTGGCCCA[C/G]GGAAGCCAAAAGATT | 267 |
rs35506094 | in-del | -/A | | | intron-variant | AMFR | GRCh38.p7 | 16:56416931 | GAGTATACTGATACT[-/A]AAAAGGGAATTTATG | 267 |
rs35593906 | in-del | -/A | | | intron-variant | AMFR | GRCh38.p7 | 16:56409716 | CTAATACTTGTCCTC[-/A]AGAAAACAGAAAAAA | 267 |
rs35621896 | in-del | -/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56378193 | TGTCTAAAAGATTTA[-/T]TTACAAAGCAACAGT | 267 |
rs35626903 | snp | A/G | 0.478603 | 0.101197 | intron-variant | AMFR | GRCh38.p7 | 16:56397701 | ACATATATTTTATAT[A/G]TAATCATTTATAATA | 267 |
rs35630803 | snp | A/C | 0.480931 | 0.0957637 | intron-variant | AMFR | GRCh38.p7 | 16:56397744 | ATTTATAATATATAA[A/C]TGTATCATTTATAAT | 267 |
rs35765211 | in-del | -/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56387968 | TGCCCATATTGACAT[-/G]GGAATCAGGCAAAAT | 267 |
rs35866917 | in-del | -/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56416136 | GTTTTTACATGTAGT[-/C]CAGTCATATGAATTT | 267 |
rs36081467 | in-del | -/A | | | intron-variant | AMFR | GRCh38.p7 | 16:56382193 | ATATTACTCAGCCTT[-/A]AAAAGGAAGAAAATT | 267 |
rs36105447 | in-del | -/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56391429 | AAGCGCAAGGGGTCA[-/G]GGGAATTCCCCTTCA | 267 |
rs36110886 | in-del | -/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56371018 | GCTCTTGCTGGGGGT[-/G]GGAATGTTGGCAACA | 267 |
rs36113919 | in-del | -/AA | | | intron-variant | AMFR | GRCh38.p7 | 16:56382533 | AAAAAAAAAAAAAAA[-/AA]GGCAAAAAAATCTCA | 267 |
rs55677376 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56417773 | TATGTATATGCAAAT[A/T]TTCCAAAATCCAGGA | 267 |
rs55724939 | snp | A/G | 0.425432 | 0.178112 | intron-variant | AMFR | GRCh38.p7 | 16:56396207 | CATATGGAACCAAAA[A/G]AGAGCCTGCATTGCC | 267 |
rs55977160 | in-del | -/A/AA/AAA | | | intron-variant | AMFR | GRCh38.p7 | 16:56366401 | AAAAAAAAAAAAAAA[-/A/AA/AAA]CTGGAAATGTAGACA | 267 |
rs56173007 | in-del | -/AA | | | intron-variant | AMFR | GRCh38.p7 | 16:56387111 | AAAAAAAAAAAAAAA[-/AA]TCAAGTGGAATGGCT | 267 |
rs56179561 | snp | A/G | 0.291493 | 0.246533 | intron-variant | AMFR | GRCh38.p7 | 16:56383566 | TGCCTGTTCCTCCCG[A/G]GTCTTCGCATCTCAG | 267 |
rs56215299 | in-del | -/A | | | intron-variant | AMFR | GRCh38.p7 | 16:56402539 | CCAGCTTGGCAAAAA[-/A]GTGCCTCCTTCAATG | 267 |
rs57103530 | in-del | -/ACAC | | | intron-variant | AMFR | GRCh38.p7 | 16:56384734 | CACACACACACACAC[-/ACAC]TCAATTTTTGGAGGT | 267 |
rs58541339 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56419230 | GTTTCACCATGTTGG[C/T]CAGGCTGGTCTCAAT | 267 |
rs58601245 | in-del | -/C/CAAAACAAAACAA | | | intron-variant | AMFR | GRCh38.p7 | 16:56374413 | TAAAAAAAAAAAAAA[-/C/CAAAACAAAACAA]AAAAAAAAAACACTA | 267 |
rs59340731 | in-del | -/A | | | intron-variant | AMFR | GRCh38.p7 | 16:56418184 | AAAAAAAAAAAAAAA[-/A]CTGCTTAAAAAAAGT | 267 |
rs59418620 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56419245 | TCAGGCTGGTCTCAA[A/T]CTCCTGACCTCAGGT | 267 |
rs59948597 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56419144 | TTCTCCTGCCTCAGC[C/T]TCCCAAGTAGCTGAG | 267 |
rs59991090 | in-del | -/AAACAAAACAAAAC/C/CAAAACAAAAC | | | intron-variant | AMFR | GRCh38.p7 | 16:56374415 | AAAAAAAAAAAAAAA[-/AAACAAAACAAAAC/C/CAAAACAAAAC]AAAAAAAACACTACA | 267 |
rs60448984 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56370908 | CCTCCTGAGATATTA[A/G]CTCCTAGGGACACGT | 267 |
rs61143587 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56385274 | CCCAGCCTCATAAAA[A/T]TTTTAATAAAAGGCA | 267 |
rs61269975 | in-del | -/T | 0.484771 | 0.0859212 | intron-variant | AMFR | GRCh38.p7 | 16:56384805 | GTGAGCCTCATGCAA[-/T]TTTTTTTTTTTTTGA | 267 |
rs61405483 | snp | A/G | 0.289942 | 0.246789 | intron-variant | AMFR | GRCh38.p7 | 16:56386428 | CCAGCGCCCTCACAC[A/G]CTCAGCCTGGGAGAT | 267 |
rs61548096 | in-del | -/AAT | 0.423984 | 0.179526 | intron-variant | AMFR | GRCh38.p7 | 16:56402335 | AGACTCCATCTCCAA[-/AAT]AATAATAATAATAAT | 267 |
rs62035979 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56374053 | GCACACTTGTAATCC[C/T]AGCTACTGGGGAGGC | 267 |
rs62035980 | snp | G/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56374061 | GTAATCCCAGCTACT[G/T]GGGAGGCTGAGGCAG | 267 |
rs62035981 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | AMFR | GRCh38.p7 | 16:56377434 | AACACCCATTCATGA[G/T]AAAAACTCTCAGTAA | 267 |
rs62035982 | snp | A/C | | | missense | AMFR | GRCh38.p7 | 16:56389188 | AAACCAACTAACCAT[A/C]GAAATGGAAGAAGTG | 267 |
rs62035983 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56419038 | TTTTTTTTTTTTTTA[A/T]TTTTAGACAGAGTCT | 267 |
rs62035984 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56420869 | TACAGCACAGGCCAC[A/T]ACACTTAATTTGCAT | 267 |
rs62035985 | snp | G/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56421130 | TTTTTTTTTTTTTTG[G/T]TAGAGCAGGGGGTCT | 267 |
rs62035986 | snp | C/T | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56422583 | CTGTCCTCCCCACGC[C/T]AGACCGAGCTCCACA | 267 |
rs67179399 | snp | A/G | 0.479502 | 0.0991411 | intron-variant | AMFR | GRCh38.p7 | 16:56406289 | ATTACAGAAATTGAC[A/G]GCCAGGTACAGTGGC | 267 |
rs71387117 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | AMFR | GRCh38.p7 | 16:56406368 | TTGATCTCAGGAGTT[C/T]AAGACCAGCCTGGTA | 267 |
rs71863980 | in-del | -/AC | | | intron-variant | AMFR | GRCh38.p7 | 16:56384704 | CACACATGCATACAT[-/AC]ACACACACACACACA | 267 |
rs72814472 | snp | G/T | 0.247905 | 0.249991 | intron-variant | AMFR | GRCh38.p7 | 16:56382111 | CGATAGCTAAAATGT[G/T]GAAGCAATGTGAGTG | 267 |
rs72814474 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AMFR | GRCh38.p7 | 16:56383581 | AGTCTTCGCATCTCA[A/G]TACGTGGTACCACTG | 267 |
rs72814484 | snp | C/T | 0.21695 | 0.247806 | intron-variant | AMFR | GRCh38.p7 | 16:56423207 | ATATACACTGAGTGA[C/T]GAGACAAACAGTGAG | 267 |
rs73545935 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | AMFR | GRCh38.p7 | 16:56369728 | TATGTTTATTGCAGC[A/G]CTATTCACAGTAGCA | 267 |
rs73545993 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56403615 | TACATGATAAAAAAT[A/C]TGTAAAATGTGAAAT | 267 |
rs73546000 | snp | A/G/T | 0.000132114 | 0.00812657 | missense | AMFR | GRCh38.p7 | 16:56408001 | GTGTGCATTCCGTGG[A/G/T]TGTAGCCGGTGATGG | 267 |
rs73547619 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | AMFR | GRCh38.p7 | 16:56417813 | CAAATCCAAAACTTC[A/G]GGTCCCAAGCATTTT | 267 |
rs73547636 | snp | C/T | 0.021333 | 0.101051 | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56427263 | AGACTTGAATTCACT[C/T]TGGTTCTCTTCCCAC | 267 |
rs74020999 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56365559 | ACACACACACACACA[C/G]ACACACGTAGTTGGC | 267 |
rs74023807 | snp | C/G | 0.287606 | 0.247155 | intron-variant | AMFR | GRCh38.p7 | 16:56422198 | TGACATCACACTCTA[C/G]CCTCTTCCTAGGTCA | 267 |
rs74023808 | snp | C/T | 0.289424 | 0.246872 | intron-variant, upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56424725 | CCAGCCCGTTCCTCC[C/T]CACTGCCCCTTAACC | 267 |
rs74246244 | snp | G/T | 0.111224 | 0.207945 | intron-variant | AMFR | GRCh38.p7 | 16:56418983 | AGGGAGAGAGAGAGA[G/T]CTACTTTTCACTGCA | 267 |
rs74246245 | snp | C/T | 0.175576 | 0.238665 | intron-variant | AMFR | GRCh38.p7 | 16:56423358 | TAAGAAGTGATAAAC[C/T]TGCCAGAGGTAAGAC | 267 |
rs74569246 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | AMFR | GRCh38.p7 | 16:56390042 | CTCTTCTCTTTGCAC[A/G]CTGTTTTCCCAACAA | 267 |
rs74570121 | snp | A/G | 0 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56412863 | GACGCTGTCTCAAAA[A/G]AAAAAAAAAAAAAGG | 267 |
rs74751281 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | AMFR | GRCh38.p7 | 16:56377026 | AGCCCACATGAGTTC[A/G]CTAGTGAATTCTGCC | 267 |
rs74756805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56423129 | AACAATCTTAATCTG[C/T]CCCACCACTGGGGAA | 267 |
rs74777329 | snp | C/G | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56412040 | TTATACATAATATAT[C/G]TGAAATGGTTAGACA | 267 |
rs74785381 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56406261 | TAGGCTGGTCTTGAA[C/G]GGTATTTTTTTTATT | 267 |
rs74788372 | snp | A/G | 0 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56412864 | ACGCTGTCTCAAAAG[A/G]AAAAAAAAAAAAGGC | 267 |
rs74887261 | snp | C/T | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56394891 | TACCATCAGAGAATA[C/T]TATAAACACCTCTAT | 267 |
rs75036664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56402844 | TGGGGATTCACACCC[A/G]GGCAGTCTGACTCCA | 267 |
rs75165960 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | AMFR | GRCh38.p7 | 16:56401923 | TGATAGACTGCGCCT[A/G]TATCACAACACAGTT | 267 |
rs75166029 | snp | A/C | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56406554 | TGACACCTTGTCTCA[A/C]AAAAAAAAAAAAAAA | 267 |
rs75232704 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | AMFR | GRCh38.p7 | 16:56384049 | TTGCCAGGCCCCAAC[C/T]ATAATGACCTTTCTC | 267 |
rs75260348 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | AMFR | GRCh38.p7 | 16:56366747 | AGTGCTCTGACAATA[C/T]GGTAACTGAGGAAGC | 267 |
rs75271110 | in-del | -/A | 0.143284 | 0.226079 | intron-variant | AMFR | GRCh38.p7 | 16:56416201 | GCATGTGGGAAATCA[-/A]GAAAAATGAGGGAGC | 267 |
rs75309038 | snp | G/T | 0.142609 | 0.225759 | intron-variant | AMFR | GRCh38.p7 | 16:56365255 | CTTGAGAAATCTACA[G/T]AAAGAAACTGGCAGG | 267 |
rs75315203 | snp | C/T | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56372012 | GTATCCTTCCCCCAT[C/T]TTTTTTTTTTACCTT | 267 |
rs75326660 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | AMFR | GRCh38.p7 | 16:56416094 | CCCCAGCTTTATTAC[A/G]ACGCAATTTCTTAAA | 267 |
rs75413099 | snp | A/C/T | 0.00716266 | 0.059414 | intron-variant | AMFR | GRCh38.p7 | 16:56394855 | AGGGGATATCACCAC[A/C/T]GATCCCACAGAAATA | 267 |
rs75644838 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | AMFR | GRCh38.p7 | 16:56384452 | TCAATCAATAAAGAT[G/T]AACTAATTAACGAAT | 267 |
rs75674320 | snp | C/G | 0.00296893 | 0.0384142 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362186 | GGAAATGCTGAGAGG[C/G]GAGGGGACCCATGGG | 267 |
rs75698480 | snp | C/T | 0.111224 | 0.207945 | intron-variant | AMFR | GRCh38.p7 | 16:56414874 | CTAATAATATAAATA[C/T]ATATATACAGAGAGA | 267 |
rs75705058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56404649 | TAAAAGAATAATCTA[C/T]TGACTTGGTCAGCAG | 267 |
rs75717289 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | AMFR | GRCh38.p7 | 16:56379100 | GCATTTGTATTTGTC[A/G]TTTTCTCATTGCTGA | 267 |
rs75721446 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | AMFR | GRCh38.p7 | 16:56378060 | ATCCCAATTAATATC[C/G]CAGCAAGCTATTTTG | 267 |
rs75724857 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AMFR | GRCh38.p7 | 16:56364352 | CTCACACAGAATGTT[C/T]GGCATCAGAGGGTAA | 267 |
rs75872105 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | AMFR | GRCh38.p7 | 16:56418848 | ACACGTTTGTATAAT[A/G]TGTAGGTGTGAACTG | 267 |
rs75953341 | in-del | -/GAA | | | intron-variant | AMFR | GRCh38.p7 | 16:56374079 | GAGGCTGAGGCAGAA[-/GAA]CTGCTTGAACTCAGG | 267 |
rs76021325 | snp | C/T | 0.112983 | 0.209108 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56361585 | CTTTTGAAAGATTTA[C/T]TGAAATAAATTATCT | 267 |
rs76027966 | snp | A/G | 0.288646 | 0.246995 | intron-variant | AMFR | GRCh38.p7 | 16:56398605 | ACCTGTAAATATACA[A/G]ATATTAAAAAAAAAA | 267 |
rs76136915 | snp | A/G | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56394893 | CCATCAGAGAATATT[A/G]TAAACACCTCTATGC | 267 |
rs76240050 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | AMFR | GRCh38.p7 | 16:56372058 | AAAGTGTCCCACTTT[A/G]TATCAGAGACTTGAG | 267 |
rs76246930 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | AMFR | GRCh38.p7 | 16:56387962 | CCCACCCTGCCCATA[C/T]TGACATGGAATCAGG | 267 |
rs76252171 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | AMFR | GRCh38.p7 | 16:56371276 | ACCAGAAAATCCAGC[A/T]AGTTAATTATTAGAT | 267 |
rs76268641 | snp | G/T | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56420735 | TTGTTTTTTTTTTTT[G/T]AGACCAGAGTCTCAC | 267 |
rs76314645 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | AMFR | GRCh38.p7 | 16:56384044 | CCTACTTGCCAGGCC[C/T]CAACCATAATGACCT | 267 |
rs76424910 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | AMFR | GRCh38.p7 | 16:56421787 | CTGAGCAATGTAAAA[C/T]AGCCCAGAAATGAGT | 267 |
rs76478031 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | AMFR | GRCh38.p7 | 16:56411034 | TGTACATTCCCATGG[A/G]CAGTGTGTATGCATA | 267 |
rs76492685 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | AMFR | GRCh38.p7 | 16:56366963 | CCCACTCAGCTCAGG[C/T]GGTCTCAGTTTTGCA | 267 |
rs76492985 | snp | G/T | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56420734 | TTTGTTTTTTTTTTT[G/T]GAGACCAGAGTCTCA | 267 |
rs76599437 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56370386 | AGAAACTTGATAAGT[G/T]GTTGCCAGGGGCTGA | 267 |
rs76652504 | snp | A/T | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56374400 | AAGCAGGACAAAGGT[A/T]AAAAAAAAAAAAAAA | 267 |
rs76784490 | snp | C/T | 0.143622 | 0.226238 | intron-variant | AMFR | GRCh38.p7 | 16:56383402 | AGCTCAGATGTCAGC[C/T]CTCTTCTCTTTGACC | 267 |
rs76825441 | snp | A/G | 0.166832 | 0.235761 | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56427485 | AACCAAATTTGTCCC[A/G]TCACCCTTAGAAACA | 267 |
rs76870851 | snp | C/G | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56368345 | TTCTGGGGAAATCCA[C/G]AGCCAACAGCCAGGT | 267 |
rs76876546 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | AMFR | GRCh38.p7 | 16:56413673 | CACCCAAAACAAGAA[C/T]AAATCTCCTAATTTT | 267 |
rs76955156 | snp | A/C/G | 0.00862798 | 0.0651126 | missense, synonymous-codon | AMFR | GRCh38.p7 | 16:56363944 | TTGCTGGAGGAGTTC[A/C/G]TCCTTACGCTGCACC | 267 |
rs76986150 | snp | C/T | 0.143622 | 0.226238 | intron-variant | AMFR | GRCh38.p7 | 16:56374290 | GAAGGAAAAGAGAAA[C/T]GAACACAAGAAATAT | 267 |
rs77035154 | snp | A/T | 0 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56372346 | TATTTCATGTAGCAT[A/T]AATGTCCTCCAGGTT | 267 |
rs77056150 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | AMFR | GRCh38.p7 | 16:56384628 | AAAAATACAAAGAAA[C/T]TTGAAGTATTCAAAC | 267 |
rs77071411 | snp | A/G | 0.111224 | 0.207945 | intron-variant | AMFR | GRCh38.p7 | 16:56404378 | ATTCTCACCATTATT[A/G]GATCACTGAAGGGCC | 267 |
rs77092897 | snp | A/T | 0.0283406 | 0.115616 | intron-variant | AMFR | GRCh38.p7 | 16:56420138 | AAGAGAGGAAGGTGC[A/T]TTTATCACCATGTAA | 267 |
rs77129696 | snp | C/T | 0.0341408 | 0.126114 | intron-variant, utr-variant-5-prime | AMFR | GRCh38.p7 | 16:56423670 | TATCACTTTGTTTAC[C/T]TGCTAACTCAAATGC | 267 |
rs77132693 | snp | C/T | 0.0929792 | 0.194537 | intron-variant | AMFR | GRCh38.p7 | 16:56367440 | ACTAGAGTGCGGGTT[C/T]TACCTGAGCAGAAGT | 267 |
rs77265097 | snp | A/G | 0.0179353 | 0.0929837 | intron-variant | AMFR | GRCh38.p7 | 16:56403157 | ACACGGTAAAAGCGA[A/G]CGTGAACTTGCTAGT | 267 |
rs77274295 | snp | G/T | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56407399 | ATTTCTTTTTTTTTT[G/T]GAGATGGAGTCTCGC | 267 |
rs77319701 | snp | A/T | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56394788 | GACTGCTAGCAAGAC[A/T]AATAAAGAAGAAAAG | 267 |
rs77328631 | snp | G/T | 0.143622 | 0.226238 | intron-variant | AMFR | GRCh38.p7 | 16:56379958 | ATCTACCATTCTGGG[G/T]TCTGGAGGACAGTGG | 267 |
rs77377551 | snp | G/T | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56407400 | TTTCTTTTTTTTTTT[G/T]AGATGGAGTCTCGCT | 267 |
rs77472517 | snp | G/T | 0.0275645 | 0.114116 | intron-variant | AMFR | GRCh38.p7 | 16:56423451 | TCAACAGCTTTTATG[G/T]AATGTTTTCTGAAGA | 267 |
rs77666593 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | AMFR | GRCh38.p7 | 16:56365627 | GCTGGAGTCTCACTG[C/T]CCTATTCTATCCCTC | 267 |
rs77692353 | snp | C/T | 0.149999 | 0.229128 | intron-variant | AMFR | GRCh38.p7 | 16:56383893 | ATCCTGTCAGTCCCC[C/T]GGTGGTGGTGGTGGG | 267 |
rs77709644 | snp | A/T | 0.0379877 | 0.132479 | intron-variant | AMFR | GRCh38.p7 | 16:56420674 | TGAAATAGTCAACTC[A/T]TAAAGACTAAAACCT | 267 |
rs77804016 | snp | A/C | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56394751 | CGAGACTCCGTCTCA[A/C]AAAAAAAAAAAAAAA | 267 |
rs77862965 | snp | A/G/T | 0.0107246 | 0.0724382 | intron-variant | AMFR | GRCh38.p7 | 16:56370407 | CAGGGGCTGAGGATC[A/G/T]GGGAAGGAAGTGGTT | 267 |
rs77997648 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | AMFR | GRCh38.p7 | 16:56367081 | TGCCCTAGGCCATCC[C/T]CATCTGAGTTTAGAT | 267 |
rs78017686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56399756 | TGTGAACACATTAAC[A/G]GCAACTGAACTGTAC | 267 |
rs78022251 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | AMFR | GRCh38.p7 | 16:56405414 | AAAATATTTTTATGA[C/T]CTAGAAACCCAACTT | 267 |
rs78035822 | snp | A/T | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56400951 | AAAAAAAAAAAAAAA[A/T]CTGTCAACATATGTG | 267 |
rs78104464 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | AMFR | GRCh38.p7 | 16:56419375 | CTATTTTTTAAAATT[G/T]TTTTAAAGTTTAGAA | 267 |
rs78142674 | snp | A/C | 0.0908922 | 0.192833 | intron-variant | AMFR | GRCh38.p7 | 16:56367936 | TAGCCAGTTTAAGAT[A/C]TCACACAATGCTGCA | 267 |
rs78215681 | snp | A/C | 0.143284 | 0.226079 | intron-variant | AMFR | GRCh38.p7 | 16:56421968 | GCCACCTGGAGAGGC[A/C]CCCTTGGGAGGAGGA | 267 |
rs78241235 | snp | C/T | 0.142947 | 0.22592 | intron-variant | AMFR | GRCh38.p7 | 16:56387588 | AATTATAAACATGAA[C/T]TCACAGAATTTAGCA | 267 |
rs78320574 | snp | C/T | 0.021333 | 0.101051 | intron-variant | AMFR | GRCh38.p7 | 16:56385217 | GCCATCTGCCTGCCT[C/T]GGCCTCACAAAGCTC | 267 |
rs78385178 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | AMFR | GRCh38.p7 | 16:56407093 | TACAATATTATAATA[C/T]GATAATTAACATTAT | 267 |
rs78474559 | snp | G/T | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56374816 | AGAGCATCAAAGAAG[G/T]TATAAATAAATAAAA | 267 |
rs78542784 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56405904 | GAGGTGGAAGGATGG[A/T]TTGAACCTGGGAGGT | 267 |
rs78544874 | snp | C/T | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56394776 | AAAAAATTGATAGAC[C/T]GCTAGCAAGACTAAT | 267 |
rs78690084 | snp | C/T | 0.111224 | 0.207945 | intron-variant | AMFR | GRCh38.p7 | 16:56382343 | CATAGAGAAAGCAAG[C/T]AGCATAATGGTTGCC | 267 |
rs78717258 | snp | C/T | 0 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56394818 | GAGAGAAGAATCAAA[C/T]AGATGCAGTAAAAAA | 267 |
rs78751238 | snp | A/G | 0.142609 | 0.225759 | intron-variant | AMFR | GRCh38.p7 | 16:56366699 | AAAGGCCAAGGTGGG[A/G]TTGTCCAGTTTTTAT | 267 |
rs78778232 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | AMFR | GRCh38.p7 | 16:56417829 | GGTCCCAAGCATTTT[A/G]GATAAAGTATTCTCA | 267 |
rs78813591 | snp | G/T | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56416912 | AAAAAAAAAAAAAAA[G/T]TCTGAGTATACTGAT | 267 |
rs78820665 | snp | C/T | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56394852 | TAAAGGGGATATCAC[C/T]ACCGATCCCACAGAA | 267 |
rs78859797 | snp | A/G | 0.143284 | 0.226079 | intron-variant | AMFR | GRCh38.p7 | 16:56419859 | GCTATAGTGCTGTCA[A/G]AGCTTCAAGTCATTT | 267 |
rs78879666 | snp | A/T | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56419036 | TTTTTTTTTTTTTTT[A/T]AATTTTAGACAGAGT | 267 |
rs78919872 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | AMFR | GRCh38.p7 | 16:56363399 | TGGAACAAAACCCCC[C/T]CTATCCACAGGACAC | 267 |
rs78928449 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56377382 | AAAAGTAACATGACC[A/G]TATCAGTAGATGCAG | 267 |
rs78935730 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | AMFR | GRCh38.p7 | 16:56382781 | TAAAATAGAAAAATC[A/G]AAAAAAAAATTCACT | 267 |
rs79054127 | snp | C/T | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56372013 | TATCCTTCCCCCATC[C/T]TTTTTTTTTACCTTA | 267 |
rs79373953 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant, utr-variant-5-prime | AMFR | GRCh38.p7 | 16:56423796 | TAAACAGGAACTTCA[A/C]CCTTCACTGCCTTCT | 267 |
rs79405275 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | AMFR | GRCh38.p7 | 16:56406713 | AATGTAAGAAATGAT[A/T]TAGTTTAAAATATCA | 267 |
rs79418283 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56427340 | AAGGAAAGCTTTATT[C/T]TGAAAAACTATTGTA | 267 |
rs79432832 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | AMFR | GRCh38.p7 | 16:56384117 | TACTGTTTCCACGGC[C/T]TCCTTCCCCCTGATC | 267 |
rs79486090 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | AMFR | GRCh38.p7 | 16:56373806 | AGTGAAGAATTCCCG[G/T]GACAGGCTTATTAAT | 267 |
rs79496577 | snp | A/G | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56394826 | AATCAAACAGATGCA[A/G]TAAAAAATGATAAAG | 267 |
rs79497218 | snp | A/C | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56374410 | AAGGTAAAAAAAAAA[A/C]AAAAAAAAAAAAACA | 267 |
rs79592800 | snp | A/T | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56402337 | ACTCCATCTCCAAAA[A/T]AATAATAATAATAAT | 267 |
rs79613509 | snp | A/G | 0 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56416911 | GAAAAAAAAAAAAAA[A/G]GTCTGAGTATACTGA | 267 |
rs79675544 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56381606 | AGCCATCTAAAAAGG[C/T]TACATACTGCAGGAT | 267 |
rs79698649 | snp | C/G | 0.16911 | 0.236552 | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56426734 | GATCCTCCCACCTTG[C/G]CTTCACAAAGTGCAG | 267 |
rs79767215 | snp | G/T | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56421128 | TTTTTTTTTTTTTTT[G/T]GGTAGAGCAGGGGGT | 267 |
rs79884803 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | AMFR | GRCh38.p7 | 16:56402847 | GGATTCACACCCGGG[C/T]AGTCTGACTCCAGAG | 267 |
rs79969873 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | AMFR | GRCh38.p7 | 16:56401315 | ATCCACTTCTCTGGT[A/G]TGCTCTTAAGGCTTC | 267 |
rs79979160 | snp | A/G | 0.111224 | 0.207945 | intron-variant | AMFR | GRCh38.p7 | 16:56415203 | AAAATGGAAGAGTTG[A/G]CTGTCCCCAACCCAG | 267 |
rs79980251 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | AMFR | GRCh38.p7 | 16:56377499 | AAGAATATCTACAAA[A/G]ACCCTACCACTAACA | 267 |
rs80049466 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | AMFR | GRCh38.p7 | 16:56408544 | TAGGGCTAGCACAAT[C/T]GAAATGCAATCCAGG | 267 |
rs80068720 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | AMFR | GRCh38.p7 | 16:56370404 | TGCCAGGGGCTGAGG[A/G]TCAGGGAAGGAAGTG | 267 |
rs80129653 | snp | C/T | 0.143959 | 0.226396 | intron-variant | AMFR | GRCh38.p7 | 16:56400061 | TCACTTTCCCTCGGC[C/T]GGTCTGGCATCACAC | 267 |
rs80186711 | snp | C/T | 0 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56406205 | AGTCTCTCATGGCTT[C/T]TTTTTTTTTTTTTGT | 267 |
rs80207779 | snp | C/T | 0.142609 | 0.225759 | intron-variant | AMFR | GRCh38.p7 | 16:56413564 | CACTCAAATCCTCAG[C/T]GAACTGCCAATCTAT | 267 |
rs80212345 | in-del | -/T | 0.225893 | 0.248835 | intron-variant | AMFR | GRCh38.p7 | 16:56403960 | CATGAGGAAAAAAAA[-/T]TTAAAAAAAGAAGAT | 267 |
rs80222210 | snp | G/T | 0.111928 | 0.208413 | intron-variant | AMFR | GRCh38.p7 | 16:56371462 | ACTTTTTAAAGGAGG[G/T]CGGTGGGGTGGTCCA | 267 |
rs80256139 | snp | A/C | 0.0283406 | 0.115616 | intron-variant | AMFR | GRCh38.p7 | 16:56370459 | AAGGACATGACTACA[A/C]AAGGACCTAGTGGAG | 267 |
rs111209678 | snp | C/G | 0.43598 | 0.167067 | intron-variant | AMFR | GRCh38.p7 | 16:56398142 | TTATAATATATAACT[C/G]TATCATTTATAATAT | 267 |
rs111232939 | in-del | -/T | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56375063 | AGTTGCAAATGTATA[-/T]TACAAACTCTAGGGC | 267 |
rs111248624 | snp | A/G | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56370990 | GAAAAGGTCGGCACC[A/G]GGCTCTGCTTAGAGC | 267 |
rs111257017 | snp | A/G | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56403134 | CTTAGAGAGAAAGAG[A/G]ATAAAACACACGGTA | 267 |
rs111267272 | snp | A/T | 0.0236746 | 0.106192 | intron-variant | AMFR | GRCh38.p7 | 16:56410273 | AGATTCTTACACAAT[A/T]GAAAAGATTAGACTT | 267 |
rs111283203 | snp | C/G | 0.415399 | 0.187465 | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56425677 | CTCAGGCCGGGGGGC[C/G]GGCACCCAGCATCAT | 267 |
rs111313055 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56393628 | GGCCATTACATAATG[C/G]TAAAGGGATCAATTC | 267 |
rs111393792 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | AMFR | GRCh38.p7 | 16:56381538 | ACAAGAAATGAGCTA[C/T]CAATCCCTTAAAGAT | 267 |
rs111429026 | snp | C/T | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56395986 | AAGGGATGTGAAGGA[C/T]CTCTCTTCAAGGAGA | 267 |
rs111472591 | snp | C/T | 0.111224 | 0.207945 | intron-variant | AMFR | GRCh38.p7 | 16:56366149 | TTTGGGAGGCAGAGG[C/T]GGGCGGATCATGAGG | 267 |
rs111476262 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56409421 | GCTTGGCTAAAAACT[A/C]ACATATTCAAATCGA | 267 |
rs111484381 | snp | C/T | 0.444444 | 0.157135 | intron-variant | AMFR | GRCh38.p7 | 16:56403447 | TGTAAACTCATGTAA[C/T]GTAAAATTATATAGT | 267 |
rs111506090 | snp | G/T | 0.5 | 0 | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56426881 | GTTCTATCTCAATAT[G/T]CGAATTGTATCTCAA | 267 |
rs111531653 | snp | C/T | 0.111224 | 0.207945 | intron-variant | AMFR | GRCh38.p7 | 16:56404491 | AATTAAGTGTAAAGA[C/T]TTTTTTTAATTACAA | 267 |
rs111562297 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56406105 | GGGGAGAGGGGGAGA[A/G]GGGGGAGGGGAGGGG | 267 |
rs111593152 | snp | A/C/T | 0 | 0 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56361793 | AAAAAAAGTAATCCA[A/C/T]TGGGGCATAAAACTG | 267 |
rs111649099 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | AMFR | GRCh38.p7 | 16:56372802 | ACCATCCTTGCCAAC[A/G]TGGTGAAACCCCATC | 267 |
rs111661573 | snp | C/T | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56366936 | TCAAGAAAGCCATGT[C/T]TTCCCCCCAGCCCCA | 267 |
rs111723691 | snp | C/T | 0.111224 | 0.207945 | intron-variant | AMFR | GRCh38.p7 | 16:56382184 | TACAATGAAATATTA[C/T]TCAGCCTTAAAAAGG | 267 |
rs111744284 | snp | C/T | 0.5 | 0 | synonymous-codon | AMFR | GRCh38.p7 | 16:56403041 | CCGACGAATTCGACG[C/T]TGCACCTCATGAAAC | 267 |
rs111756042 | in-del | -/A | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56410881 | GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 267 |
rs111757666 | snp | A/G | 0.0524604 | 0.153226 | intron-variant | AMFR | GRCh38.p7 | 16:56418345 | CCCATCTCTACTAAA[A/G]ATACAAAAATTAGCC | 267 |
rs111765619 | in-del | -/T | 0.249603 | 0.25 | intron-variant | AMFR | GRCh38.p7 | 16:56420723 | CTTAATTTTGTTTTG[-/T]TTTTTTTTTTTGAGA | 267 |
rs111767053 | snp | C/G | 0.143284 | 0.226079 | intron-variant | AMFR | GRCh38.p7 | 16:56405895 | TGGGAGGCAGAGGTG[C/G]AAGGATGGATTGAAC | 267 |
rs111776031 | snp | C/G | 0 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56398227 | TTTATATATATAACT[C/G]TATCATTTATATATG | 267 |
rs111801732 | snp | C/T | 0.031825 | 0.122064 | intron-variant | AMFR | GRCh38.p7 | 16:56381627 | ACTGCAGGATTCCAC[C/T]TGTATGACATTCTGG | 267 |
rs111802505 | snp | C/T | 0.0279526 | 0.114869 | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56426196 | GTACACAAATGTTGA[C/T]TACATTCTAACAATC | 267 |
rs111812519 | in-del | -/C | 0.5 | 0 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362017 | ATTTCTTTAATAAAG[-/C]CCTTCAAGGTTTACT | 267 |
rs111828052 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56361904 | CCTCTCCAAGGCAGG[C/T]AGGTTCACACCTTAC | 267 |
rs111869365 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56398164 | TTATAATATATAACT[C/G]TATCATTTATATATA | 267 |
rs111877465 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | AMFR | GRCh38.p7 | 16:56385081 | TGCTGGGATTACAGG[C/T]ATGAGCCACCATGCC | 267 |
rs111921043 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | AMFR | GRCh38.p7 | 16:56412625 | AGCACTTTGGGAGGC[C/T]GAGGCGGGCGGACTG | 267 |
rs111921441 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56395262 | TATCCCTGATGAACA[C/T]CGATGCAAAAATCCT | 267 |
rs111969603 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | AMFR | GRCh38.p7 | 16:56377903 | ATACATATAAGTTCT[A/G]TATGAGGAAAATTAC | 267 |
rs112052035 | snp | A/G | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56375135 | TTTCAATGCAGCCCA[A/G]TACAAATTTATAAAC | 267 |
rs112075432 | snp | C/T | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56379783 | CCGCTGAATCCATGT[C/T]TCGCATCTGGGTCAC | 267 |
rs112136900 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56424462 | GACGGCCTCTCTCCA[A/G]CCGGAATGTCCAAAG | 267 |
rs112145524 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56398269 | TTTATATATGTAACT[C/G]TATCATTTATATATG | 267 |
rs112155232 | snp | C/T | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56399244 | ACAGCTGCTGCACCA[C/T]TTTGGCGTTTCCTCA | 267 |
rs112221607 | snp | A/G | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56401683 | ACACAAAGCACACAC[A/G]CGCCCTGGACAGAAC | 267 |
rs112233856 | snp | A/G | 0.0766824 | 0.180169 | intron-variant | AMFR | GRCh38.p7 | 16:56398305 | GTATCATTTATATAT[A/G]TAAATGTATCATTTA | 267 |
rs112235817 | snp | A/G | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56403205 | CAGCGGAAGCTCTTC[A/G]CTGTTGGTGATGGTG | 267 |
rs112242234 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56425448 | CGCTGCCGCCGCCGC[C/T]GCCGCGCCGGGCCGG | 267 |
rs112275445 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56392907 | AACTCCAAGACACAT[A/C]ATTGTCAGATTCACC | 267 |
rs112294160 | snp | C/T | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56410814 | TTGAACCTGGGAGGT[C/T]GAGGTTGCAGGGAGC | 267 |
rs112306099 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMFR | GRCh38.p7 | 16:56363368 | GGAACACAGTGCTGG[C/T]CCTGTCCTTAAGAGC | 267 |
rs112319312 | snp | C/G | 0 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56398206 | TTTATATATATAACT[C/G]TATCATTTATATATA | 267 |
rs112327476 | snp | A/G | 0.142947 | 0.22592 | intron-variant | AMFR | GRCh38.p7 | 16:56418368 | AATTAGCCAGGGGTG[A/G]TAGTGCTCTCCTGTA | 267 |
rs112393741 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | AMFR | GRCh38.p7 | 16:56379395 | TCCCTCCCACAAAAC[A/G]TGGGAATTCAAGATG | 267 |
rs112396226 | snp | C/T | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56391637 | GCTAGCACAGCAGTG[C/T]GTGATTGAACTGCAA | 267 |
rs112401464 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | AMFR | GRCh38.p7 | 16:56381691 | AGTGGTTGCTAGAGG[C/G]TAGGGGGAGGAAAGG | 267 |
rs112471458 | snp | A/G | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56418483 | CACTCCAGCCTAGGT[A/G]ACAGAGTGAGACTCC | 267 |
rs112477043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56415702 | CAACCAGGAACAAAC[A/G]CCCAAACTAGTTGCC | 267 |
rs112533927 | snp | C/T | | | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56425745 | ACAGAGGGCACCTGC[C/T]CCGGCCGCGGCGCAG | 267 |
rs112536938 | snp | A/G | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56414194 | ATCTGAAATCATAAT[A/G]CAAAGTTTAAAAAAA | 267 |
rs112554221 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AMFR | GRCh38.p7 | 16:56364704 | GATCCTCCCAACTTA[A/G]CCTCCCAAGTAGCTG | 267 |
rs112584794 | snp | A/G | 0.444267 | 0.157354 | intron-variant | AMFR | GRCh38.p7 | 16:56398179 | CTATCATTTATATAT[A/G]TAACTCTATCATTTA | 267 |
rs112642590 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56395934 | TCCCATTCACAATTG[C/T]TTCAAAGAGAATAAA | 267 |
rs112679538 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56398288 | CATTTATATATGTAA[A/C]TGTATCATTTATATA | 267 |
rs112697010 | snp | C/G/T | 0 | 0 | splice-acceptor-variant | AMFR | GRCh38.p7 | 16:56389376 | GAACGAAGACAGGAG[C/G/T]TACCAAAAAGTCCAA | 267 |
rs112726564 | snp | A/C | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56389763 | GTCCTTGAGTCCTCC[A/C]CTCTGACGCTCATGT | 267 |
rs112751572 | snp | C/G | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56388244 | CTGTACAGCATGTTA[C/G]TATACTGAATGCTGT | 267 |
rs112781249 | snp | C/T | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56410752 | CTGAGCATGGTGGCA[C/T]AAGCCTGTAATCCCA | 267 |
rs112787893 | snp | C/T | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56405288 | AAAATGTAGCATTGC[C/T]CAGGCCAAACTTTTT | 267 |
rs112801442 | snp | C/T | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56422764 | ATCCCCTATAAAATT[C/T]TGCCATATTACTGAG | 267 |
rs112881570 | snp | C/T | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56386222 | CTATTATCATTCTTA[C/T]AGTATCCTTCTCAAA | 267 |
rs112902024 | snp | C/T | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56399798 | GTTAAATGTATGTTA[C/T]CTGAATTTTGCCTCA | 267 |
rs112907642 | in-del | -/ACAC | 0.498392 | 0.028309 | intron-variant | AMFR | GRCh38.p7 | 16:56384704 | CACACATGCATACAT[-/ACAC]ACACACACACACACA | 267 |
rs112956946 | snp | C/T | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56375500 | AATGGCCTAAATGTG[C/T]CAAGTAAGAGAGGTT | 267 |
rs112958978 | snp | C/G | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56387592 | ATAAACATGAACTCA[C/G]AGAATTTAGCAGTAC | 267 |
rs112966884 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56393964 | ATAGTTGGAAGTAAA[C/G]CACTTCTCAGCAAAT | 267 |
rs113041120 | snp | A/G | 0.44252 | 0.159487 | intron-variant | AMFR | GRCh38.p7 | 16:56398221 | CTATCATTTATATAT[A/G]TAACTCTATCATTTA | 267 |
rs113045696 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56394868 | ACCGATCCCACAGAA[A/T]TACAAACTACCATCA | 267 |
rs113046916 | snp | C/G | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56397070 | AGGAAAACTTTTACA[C/G]TGTTGGTGGGACTGT | 267 |
rs113053769 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56392534 | AGGACCTGACGGAGC[C/T]GAAAACCATGGCACG | 267 |
rs113127022 | in-del | -/A | 0.5 | 0 | downstream-variant-500B | AMFR | GRCh38.p7 | 16:56361212 | CTACACACTTACCTG[-/A]AAAAAAAAAAGATAT | 267 |
rs113291129 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56425442 | CGCTGCCGCTGCCGC[C/T]GCCGCCGCCGCGCCG | 267 |
rs113303991 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | AMFR | GRCh38.p7 | 16:56406507 | AGGTGGAAGTTGCAG[C/T]AAGCAACTGCACTCC | 267 |
rs113313537 | snp | C/T | 0.5 | 0 | downstream-variant-500B | AMFR | GRCh38.p7 | 16:56361369 | CAAAATGGGGTTTAA[C/T]GTTGGCACCTCTGGA | 267 |
rs113341275 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | AMFR | GRCh38.p7 | 16:56363506 | GGCAGAGTGGTCAAC[A/G]GGGAGGACCTGGGAG | 267 |
rs113344940 | snp | A/G | 0.0024 | 0.0345578 | intron-variant | AMFR | GRCh38.p7 | 16:56379573 | ATCTCATCTGAGATA[A/G]GGCAAGTCCCTAACG | 267 |
rs113372897 | snp | C/T | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56399145 | CGAGAATGGCTATAA[C/T]AACAAAAATAGAAAA | 267 |
rs113393447 | snp | C/T | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56422950 | ATTACAATATGTTAA[C/T]ATCTAGCAGGACTTG | 267 |
rs113422309 | snp | C/T | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56365551 | TAACATGTACACACA[C/T]ACACACAGACACACG | 267 |
rs113425307 | snp | A/G | 0 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56398200 | CTATCATTTATATAT[A/G]TAACTCTATCATTTA | 267 |
rs113480443 | snp | A/G | 0.21695 | 0.247806 | intron-variant | AMFR | GRCh38.p7 | 16:56397496 | GAACAGCTGGACACA[A/G]GAAGGGGAACATCAC | 267 |
rs113534159 | snp | A/C | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56416811 | CCAAAAAAAGGTAAA[A/C]GTCTCTTATAATCCC | 267 |
rs113535310 | snp | C/G | 0.444444 | 0.157135 | intron-variant | AMFR | GRCh38.p7 | 16:56372661 | AGTGATCATTCCTAT[C/G]CACATACCAGATGTG | 267 |
rs113538998 | snp | A/G | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56387631 | TGAAAATCAACAGCA[A/G]CTTAATGTGAATTAA | 267 |
rs113674566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56402066 | TGCTAGGCCGAGCGC[A/G]GTGGCTTATACCTGT | 267 |
rs113730898 | snp | C/G | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56364401 | GAAAAACGTAAGCAC[C/G]TTCAAGCTGCACTCT | 267 |
rs113756701 | snp | A/C | 0.0718919 | 0.175435 | intron-variant | AMFR | GRCh38.p7 | 16:56397722 | ATTTATAATATATAA[A/C]TGTATCATTTATAAT | 267 |
rs113786292 | snp | C/T | 0.444444 | 0.157135 | intron-variant | AMFR | GRCh38.p7 | 16:56392380 | AATGACTTTGACAAG[C/T]TGAGAGAAGAAGGCT | 267 |
rs113912503 | snp | C/G | 0.415399 | 0.187465 | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56425815 | CCTCAGGGCGCGGGG[C/G]ACCCTGGCCACCAGG | 267 |
rs113922838 | snp | A/G | 0.444444 | 0.157135 | intron-variant | AMFR | GRCh38.p7 | 16:56372762 | AGGCCGAGGCAGGTG[A/G]ATCACTTGAGGTCAG | 267 |
rs113952048 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56394539 | ATGAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT | 267 |
rs113955041 | snp | C/G/T | 1.66294e-05 | 0.00288347 | splice-donor-variant | AMFR | GRCh38.p7 | 16:56409423 | TTGGCTAAAAACTCA[C/G/T]ATATTCAAATCGATC | 267 |
rs113963029 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56394396 | GAGACACAAAAAACC[C/G]TTCAAAAAAATCAGT | 267 |
rs113966472 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | AMFR | GRCh38.p7 | 16:56411282 | CACTCTGTCATCCTG[A/G]CTGGAGTGCAGTGGC | 267 |
rs113981346 | snp | A/T | 0.5 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56398341 | ATATAAATGTATCAT[A/T]TATATAATATATCAT | 267 |
rs114248966 | snp | C/G | 0.0379877 | 0.132479 | intron-variant | AMFR | GRCh38.p7 | 16:56421030 | AGAGCCTAAAATATT[C/G]ACCATCTGAGAGCAC | 267 |
rs114286060 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | AMFR | GRCh38.p7 | 16:56381893 | GCTGAGGGATGTTGA[C/T]AATGGGGAAGGCTGT | 267 |
rs114315880 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | AMFR | GRCh38.p7 | 16:56380323 | ACACAGCACAGGGAC[A/C]CTGAGCATGACCCAC | 267 |
rs114468837 | snp | A/C/G | 0.0154673 | 0.0866868 | intron-variant | AMFR | GRCh38.p7 | 16:56365639 | CTGTCCTATTCTATC[A/C/G]CTCTCCTCTAAGCCT | 267 |
rs114551141 | snp | C/T | 0.00242122 | 0.0347095 | intron-variant | AMFR | GRCh38.p7 | 16:56414233 | GTCACAAGAATCCAT[C/T]CTTTCAGTGTAGACT | 267 |
rs114621303 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | AMFR | GRCh38.p7 | 16:56386710 | GCCTAAGATACAACA[A/G]CACCAAGAATTGGCT | 267 |
rs114686065 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | AMFR | GRCh38.p7 | 16:56381566 | GATATAAAGGAAACA[C/T]ACATGCAAATAATTA | 267 |
rs114812128 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | AMFR | GRCh38.p7 | 16:56369592 | TCCCAAGAGAGGCTC[A/G]ACTAGAATATTCCAG | 267 |
rs115014703 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | AMFR | GRCh38.p7 | 16:56402060 | AATGGTTGCTAGGCC[A/G]AGCGCGGTGGCTTAT | 267 |
rs115349083 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | AMFR | GRCh38.p7 | 16:56418852 | GTTTGTATAATATGT[A/T]GGTGTGAACTGTCAA | 267 |
rs115429770 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | AMFR | GRCh38.p7 | 16:56406990 | ATTTTCTGTCAAGAC[G/T]AAATACGGTTGTATA | 267 |
rs115532716 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | AMFR | GRCh38.p7 | 16:56401419 | ACTCCCCGCTAATCC[C/T]TTCTTTTAAATCTTA | 267 |
rs115587935 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | AMFR | GRCh38.p7 | 16:56369738 | GCAGCGCTATTCACA[A/G]TAGCAAAAATATGGA | 267 |
rs115599630 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | AMFR | GRCh38.p7 | 16:56410490 | TTGTTAGAACCTTAA[C/T]AATGTCAATGAATAT | 267 |
rs115656962 | snp | C/G | 0.0170251 | 0.090679 | intron-variant | AMFR | GRCh38.p7 | 16:56403922 | ATACATAAAAAGAAG[C/G]AGTTAAATACAAAAA | 267 |
rs115787470 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | AMFR | GRCh38.p7 | 16:56363386 | TGTCCTTAAGAGCTG[A/G]AACAAAACCCCCTCT | 267 |
rs115791132 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | AMFR | GRCh38.p7 | 16:56368112 | TTACTCTGTGAACAC[A/C]CCAGTTCCTCATCTC | 267 |
rs115824911 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | AMFR | GRCh38.p7 | 16:56412148 | TCATTTTAGATATTC[A/G]ATGTCTTTGCCTCTA | 267 |
rs115927375 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | AMFR | GRCh38.p7 | 16:56375213 | TATCATTATTGTTAG[G/T]GTATTTTATGTGTGG | 267 |
rs115949894 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant, utr-variant-5-prime | AMFR | GRCh38.p7 | 16:56423996 | CCCCAAATGGGAACA[A/T]GCAAGGAGACAAGAT | 267 |
rs116168415 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | AMFR | GRCh38.p7 | 16:56412381 | CCTCTGGATCTAGTT[A/T]AAAAATCTCTAAAAT | 267 |
rs116253811 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | AMFR | GRCh38.p7 | 16:56390523 | TACTTCTTAATCACT[C/T]TGTGTCATAAGAGTG | 267 |
rs116343491 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | AMFR | GRCh38.p7 | 16:56410448 | AACACATTACTTTTT[A/G]TACAATGCTTTCTTT | 267 |
rs116516567 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | AMFR | GRCh38.p7 | 16:56414815 | ACAAATAGGAGGTAG[A/G]GGTAGGAGTGTGGAT | 267 |
rs116516858 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | AMFR | GRCh38.p7 | 16:56365313 | CTGTGACGGGAGCAC[A/G]TTCACCTTCCACTGA | 267 |
rs116655831 | snp | A/T | 0.030278 | 0.119257 | intron-variant | AMFR | GRCh38.p7 | 16:56376789 | GGAGTCAACAGAGAA[A/T]AATCAATGAAACCAA | 267 |
rs116748928 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AMFR | GRCh38.p7 | 16:56402810 | GAAGTAAATTGCCCC[A/G]AATCACACAGCACCT | 267 |
rs116753933 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | AMFR | GRCh38.p7 | 16:56382904 | GGCTGTTAAGGGGGC[A/G]TGGGAGCTGGGCACA | 267 |
rs116817692 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | AMFR | GRCh38.p7 | 16:56377319 | AAGGCTGGTTCAACA[C/T]TTGAAAATCAATTAA | 267 |
rs116828476 | snp | G/T | 0.0221141 | 0.102801 | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56426343 | GAACCTTAAACACGT[G/T]CTAAGTCAAAGAAGA | 267 |
rs116869519 | snp | A/T | 0.0298908 | 0.118541 | intron-variant | AMFR | GRCh38.p7 | 16:56377837 | AGTGGAATTTGAAAT[A/T]AAAAGCGCAGTATGC | 267 |
rs116870609 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | AMFR | GRCh38.p7 | 16:56409904 | CAGGCGCAGTGGCTC[A/G]TATCTGTAACCCCAG | 267 |
rs116895221 | snp | C/T | 0.00554273 | 0.0523511 | intron-variant | AMFR | GRCh38.p7 | 16:56401890 | TCAGTCAGTTCCACA[C/T]GCACACTAAACACCA | 267 |
rs116902295 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | AMFR | GRCh38.p7 | 16:56409243 | CTCCCCAGGAGACAA[C/T]GATTCTGCATCTCTT | 267 |
rs116904226 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56423379 | GAGGTAAGACCTCTA[C/T]TGAAAATGCTGGAAG | 267 |
rs116915855 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | AMFR | GRCh38.p7 | 16:56383395 | AACCTAGAGCTCAGA[G/T]GTCAGCCCTCTTCTC | 267 |
rs116941540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56402054 | CTAAATAATGGTTGC[C/T]AGGCCGAGCGCGGTG | 267 |
rs116976744 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | AMFR | GRCh38.p7 | 16:56387523 | TCAAATCAGGGATGC[A/G]AATAGCACTACTGCT | 267 |
rs117035805 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | AMFR | GRCh38.p7 | 16:56405102 | GAATTTGGTTTAACC[A/G]TGTTGTAATTTAGTC | 267 |
rs117062182 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | AMFR | GRCh38.p7 | 16:56388311 | TCTAAACATATCTAA[C/T]AGAAAACATACAGTA | 267 |
rs117067608 | snp | A/G | 0.0341408 | 0.126114 | intron-variant, upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56424682 | CCTCTGAGATCTTCT[A/G]GTTTCTCCCGAGGGT | 267 |
rs117157028 | snp | A/G | 0.0186114 | 0.0946537 | intron-variant | AMFR | GRCh38.p7 | 16:56369177 | CATTTATCATGCTTT[A/G]AAAGCCCAGTTTTAC | 267 |
rs117230138 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | AMFR | GRCh38.p7 | 16:56420316 | CCACTCCCCTGCGCC[C/T]CCTACCATTTGGTGG | 267 |
rs117262820 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | AMFR | GRCh38.p7 | 16:56403708 | CAGCTATCTGATGAT[A/G]TTTTTATCCTGAAAG | 267 |
rs117372390 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | AMFR | GRCh38.p7 | 16:56402413 | AAATCAGAGGAGTAA[A/G]GCCCCCAGAGATCCA | 267 |
rs117422530 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | AMFR | GRCh38.p7 | 16:56412679 | AACCTGGGCAGCATG[A/G]TGAAATTCCGTCTCT | 267 |
rs117434276 | snp | A/C | 0.0295035 | 0.117819 | intron-variant | AMFR | GRCh38.p7 | 16:56373488 | CCCGACACCTACATC[A/C]CGACAGGCCTGTTCA | 267 |
rs117456520 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56391164 | TTGTTCACTCAACCC[A/G]AGGCAGATAAGTGTT | 267 |
rs117538569 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56398970 | GGTGATGAAGGCTGT[A/C/G]CAACAATGTGATTGT | 267 |
rs117547856 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | AMFR | GRCh38.p7 | 16:56417444 | AATATTGTGTCATAC[A/G]TATAACTTCTCAACT | 267 |
rs117568276 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | AMFR | GRCh38.p7 | 16:56421951 | CAATGTCATGCCTGA[A/G]GGCCACCTGGAGAGG | 267 |
rs117590507 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | AMFR | GRCh38.p7 | 16:56365773 | TAATACCAGCCTGAG[C/T]GGGGCAGGGCAGAGA | 267 |
rs117598649 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | AMFR | GRCh38.p7 | 16:56377731 | GAACTGATAAAAACA[C/T]TCTTGGAACTAATAA | 267 |
rs117639894 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | AMFR | GRCh38.p7 | 16:56390389 | CTTTTAAATATCTAC[A/G]AACATGTGTAGATAT | 267 |
rs117766610 | snp | A/C | 0.0327778 | 0.123752 | intron-variant | AMFR | GRCh38.p7 | 16:56375546 | GAAAACCAAGACCTA[A/C]CTGAATGTTGTTTAC | 267 |
rs117779408 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | AMFR | GRCh38.p7 | 16:56379798 | CTCGCATCTGGGTCA[C/T]GCTGATGCAAGAGAC | 267 |
rs117877004 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56408429 | GTATACAACTCTCTC[A/C]TCTCACCTTCAACAG | 267 |
rs117881378 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | AMFR | GRCh38.p7 | 16:56399234 | ATCAAGTGGTACAGC[C/T]GCTGCACCACTTTGG | 267 |
rs117914597 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | AMFR | GRCh38.p7 | 16:56370207 | ATCTTGGGTATAAAA[A/T]TGTGTTTTCCTTAAA | 267 |
rs117943434 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | AMFR | GRCh38.p7 | 16:56363133 | CAGAAGGTTGATTTC[A/G]CATCTCCCCATGTCC | 267 |
rs117979090 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | AMFR | GRCh38.p7 | 16:56416260 | AGAATCTACAAGAGA[C/T]AGAGCATGGTAAGCA | 267 |
rs118005810 | snp | A/T | 0.0387552 | 0.1337 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56361535 | AATTAAAAAAAAAAA[A/T]CACAGAAATTTACTA | 267 |
rs118006268 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | AMFR | GRCh38.p7 | 16:56402440 | TCCAATCTGTGTCCC[C/T]GGCCACAAAGAAGAG | 267 |
rs118085126 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | AMFR | GRCh38.p7 | 16:56376810 | ATGAAACCAAAAGCC[A/G]GTCCTTTGAAATGAT | 267 |
rs137888419 | snp | A/G | 0.110872 | 0.20771 | intron-variant | AMFR | GRCh38.p7 | 16:56398316 | ATATATAAATGTATC[A/G]TTTATATATATATAA | 267 |
rs137951767 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | AMFR | GRCh38.p7 | 16:56364827 | CTGGACTCAAGCAAT[C/T]TACCCACCTCAGCCT | 267 |
rs138015419 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | AMFR | GRCh38.p7 | 16:56382226 | GACTTGTGCTACAAC[A/G]TGGATGAACCATGAT | 267 |
rs138050993 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56393808 | AGATCAACGAGACAG[A/C]AAGTTAACAAGGATA | 267 |
rs138094163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56408658 | TCCTGAGGTCACAGG[C/T]GGAGATTAAAAAAAA | 267 |
rs138111740 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56372654 | GCCCCTCAGTGATCA[C/T]TCCTATGCACATACC | 267 |
rs138148922 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | AMFR | GRCh38.p7 | 16:56391990 | GACTGACACTTCACA[C/T]GGCGGGGTACCCCTC | 267 |
rs138195916 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56422856 | AGGTTTTAAATTGTG[A/T]TTGTTCATGAAAAAC | 267 |
rs138221964 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56418976 | AGGTAACAGGGAGAG[A/C]GAGAGATCTACTTTT | 267 |
rs138247111 | snp | A/C | 9.97738e-05 | 0.00706236 | missense | AMFR | GRCh38.p7 | 16:56364039 | CCTCACTGGGCTCCA[A/C]TTCCACCTCGCCGAA | 267 |
rs138279117 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56397232 | CACATGCACACGTTA[A/T]GTTTATTGTGGCACT | 267 |
rs138329983 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56409701 | TCTGCACTTGGCTTT[C/T]TAATACTTGTCCTCA | 267 |
rs138438994 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56410118 | GGTCAAGGCTACAGT[C/G]AGCCATCATCATGCC | 267 |
rs138515706 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56372230 | AACTATATCTAAGGG[A/G]CAACACTCCTATTTC | 267 |
rs138669379 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | AMFR | GRCh38.p7 | 16:56403514 | TACTATTATATTTGT[A/G]TATATAACAGTTCTG | 267 |
rs138682084 | snp | A/G | 1.67775e-05 | 0.00289629 | missense | AMFR | GRCh38.p7 | 16:56362991 | ACGGGGTCAGAGGAC[A/G]CACCTTCCGAGGGGA | 267 |
rs138700051 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56414492 | TAAGGAATATCTGAA[A/G]AGGCACACTGTTCTG | 267 |
rs138787475 | in-del | -/TAGA | 0.216349 | 0.247725 | intron-variant | AMFR | GRCh38.p7 | 16:56390877 | GTGAGTACAACTAGT[-/TAGA]TATAGTTTTCTGTTT | 267 |
rs138818558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56383592 | CTCAGTACGTGGTAC[C/T]ACTGTCAACTCAGCT | 267 |
rs138846860 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMFR | GRCh38.p7 | 16:56377025 | CAGCCCACATGAGTT[C/T]GCTAGTGAATTCTGC | 267 |
rs138857665 | snp | A/C/T | 4.94224e-05 | 0.00497083 | synonymous-codon | AMFR | GRCh38.p7 | 16:56367504 | CACAGGACTGTTCAA[A/C/T]GCAGGTCTGATGCTA | 267 |
rs138964886 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | AMFR | GRCh38.p7 | 16:56378852 | ACAAGTTGCTCCACA[C/T]CATATGTCATTAGAT | 267 |
rs139030301 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | AMFR | GRCh38.p7 | 16:56417188 | GCCAAGGTGGGGGGA[C/T]TGCTTGAACTCAGGA | 267 |
rs139163917 | in-del | -/CTAA | 0.0185938 | 0.0946107 | intron-variant | AMFR | GRCh38.p7 | 16:56399927 | CAAGCTCCTTAGGGG[-/CTAA]CTAATTTTGAGAAAT | 267 |
rs139222832 | snp | C/G/T | 0.00122035 | 0.0246718 | synonymous-codon | AMFR | GRCh38.p7 | 16:56405002 | CCCCTTTCCTTCCCA[C/G/T]GTCCCTTCGTGGTTG | 267 |
rs139347713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56384537 | CTAATCCAAGCAGGA[C/T]TAAGGTGGTTTGCAC | 267 |
rs139382901 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | AMFR | GRCh38.p7 | 16:56396800 | CTGACAAAAGGCTAA[C/T]ATCCAGAATCTACAA | 267 |
rs139429385 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMFR | GRCh38.p7 | 16:56389770 | AGTCCTCCACTCTGA[C/T]GCTCATGTCTTTCAC | 267 |
rs139432334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56373453 | CTAATCCCAGGACTA[C/T]AGCATGCTTCTTTCC | 267 |
rs139471216 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56385342 | TGGCTAAAGGCTGTA[C/T]GCAGTGGCTCACGCC | 267 |
rs139471961 | snp | G/T | 0.0221141 | 0.102801 | intron-variant | AMFR | GRCh38.p7 | 16:56394463 | ATTGATAGACTGCTG[G/T]CCGGGCGCAGTGGCT | 267 |
rs139530029 | snp | A/G | 1.69651e-05 | 0.00291243 | missense | AMFR | GRCh38.p7 | 16:56385950 | GAGTTGCTGGCCTGC[A/G]TAATGCCAAGAATGT | 267 |
rs139577078 | snp | A/C | 0.426813 | 0.17674 | intron-variant | AMFR | GRCh38.p7 | 16:56398118 | ATTTATAATATATAA[A/C]TGTATCATTTATAAT | 267 |
rs139676755 | snp | C/T | 0.030278 | 0.119257 | intron-variant | AMFR | GRCh38.p7 | 16:56411423 | TTTTATATTTATATT[C/T]TGCAGAGATGGGGCC | 267 |
rs139683928 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AMFR | GRCh38.p7 | 16:56404246 | TTTCTTTAAAAAGTA[C/T]GTTTTCAAAGTTTCT | 267 |
rs139783017 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56414698 | GTCCTTCCCAAGTAC[C/T]TCATTTCCGACATTA | 267 |
rs139829394 | in-del | -/CTC | 0.0248432 | 0.108648 | intron-variant | AMFR | GRCh38.p7 | 16:56422470 | TCCTTCACCCCCGGT[-/CTC]CTCTTCACCTTCTCA | 267 |
rs139858630 | snp | C/T | 0.000285525 | 0.0119449 | intron-variant | AMFR | GRCh38.p7 | 16:56404889 | TGCCCTCTGTTAGAG[C/T]TCCTTCTGAGGAAAC | 267 |
rs139867819 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56419127 | CTCCCAGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 267 |
rs139897048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56400166 | TTTAGATGGAGTTTC[A/G]TTCTTGTTGCCCAGG | 267 |
rs139897271 | in-del | -/G | 0.0154538 | 0.0865337 | downstream-variant-500B | AMFR | GRCh38.p7 | 16:56361211 | GCTACACACTTACCT[-/G]AAAAAAAAAAAGATA | 267 |
rs139938446 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56405688 | AGCAGAAAAAAGAAC[A/G]AAAGCAATCAAAAGC | 267 |
rs140020747 | snp | C/G | 0.000627249 | 0.0176983 | intron-variant | AMFR | GRCh38.p7 | 16:56367569 | GTCCAGAGTCACACA[C/G]AAATCAAATCACAGA | 267 |
rs140123120 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56377884 | CAAAACAAAATAGGA[C/T]AAAATACATATAAGT | 267 |
rs140149893 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56378223 | TAATCAAGACAATGC[A/G]GTATTGGCAAAAGAA | 267 |
rs140206887 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | AMFR | GRCh38.p7 | 16:56380425 | CCTGGAGATATTTTC[C/T]CCATTGTCTTGGGGA | 267 |
rs140265076 | in-del | -/T | 0.0349115 | 0.127424 | intron-variant | AMFR | GRCh38.p7 | 16:56410061 | ACCTGTAGTCCCACC[-/T]TACTCAGGAGGCTAA | 267 |
rs140266974 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56402040 | CACAGGAACTTTGTC[C/T]AAATAATGGTTGCTA | 267 |
rs140279056 | snp | A/G | 0.371177 | 0.218669 | intron-variant, upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56424996 | CGGAGGGGCCCCTAG[A/G]CCCACCACGCCCCCG | 267 |
rs140286780 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | AMFR | GRCh38.p7 | 16:56421471 | ACGAGTTTGCCAATC[A/C]CTGTTCTAAATGGTC | 267 |
rs140320244 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56419695 | GCTACTTGGGTGGCT[A/G]AGGCAGGAGAATTGC | 267 |
rs140367993 | snp | A/T | 0.000115131 | 0.00758632 | intron-variant | AMFR | GRCh38.p7 | 16:56408162 | TCTTCTTCATGGAAG[A/T]GTTAAACTTCACTGA | 267 |
rs140559057 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56364424 | TGCACTCTTAGAATA[C/T]GCTACCAACACGACA | 267 |
rs140571155 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56421889 | TCAGGTCAAACCCAC[A/G]TATTTGTTAGTGTAA | 267 |
rs140735267 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AMFR | GRCh38.p7 | 16:56368597 | CATCAAAGTAGAGAT[C/T]TGAGCTTTTCAAAAA | 267 |
rs140788470 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56406875 | GATAATATTATATTA[G/T]TTGAAAGTTAGAGAA | 267 |
rs140819075 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AMFR | GRCh38.p7 | 16:56386075 | CTGACTCTTTCCCCC[A/G]TCATCTGCTCTCACG | 267 |
rs140852229 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMFR | GRCh38.p7 | 16:56412114 | CTTCCTTGCTCTAAA[C/T]CTCCACTTAACATTT | 267 |
rs140864416 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56371891 | ATTCCTAAACAATAC[A/C]GTGTATAACAACCAT | 267 |
rs140928889 | snp | C/T | 0.00124733 | 0.0249421 | intron-variant | AMFR | GRCh38.p7 | 16:56389135 | AAAATAGTATCTGCT[C/T]AAGGGAGAACACCCC | 267 |
rs141019833 | in-del | -/CTT | 0.0174175 | 0.0916809 | intron-variant | AMFR | GRCh38.p7 | 16:56367917 | GCTGCTGTTACCGTC[-/CTT]CTAGCCAGTTTAAGA | 267 |
rs141031312 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56426305 | CATAAAAATGAACTA[A/C]TGATACATGCTACAA | 267 |
rs141059889 | snp | A/G | 0.140242 | 0.224618 | intron-variant | AMFR | GRCh38.p7 | 16:56398274 | ATATGTAACTGTATC[A/G]TTTATATATGTAAAT | 267 |
rs141131646 | snp | A/G | 0.000445056 | 0.0149107 | synonymous-codon | AMFR | GRCh38.p7 | 16:56409478 | CAGAAAGACAAGTCC[A/G]GCAAACCAGAGGCAC | 267 |
rs141167084 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | AMFR | GRCh38.p7 | 16:56372424 | AGTACTATTCTACTG[C/T]ACAGGTTTGCCATAT | 267 |
rs141276463 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | AMFR | GRCh38.p7 | 16:56398982 | TGTACAACAATGTGA[C/T]TGTACTTCATGCCAC | 267 |
rs141277998 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56386762 | GCTACACATTTAAGG[C/T]TGCTTTTCATTCCTT | 267 |
rs141362648 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56374192 | GAAAAGCAAACAGAA[A/T]AAAAACTGAAAATAA | 267 |
rs141387453 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | AMFR | GRCh38.p7 | 16:56382103 | ATTATTCACGATAGC[C/T]AAAATGTGGAAGCAA | 267 |
rs141411462 | snp | A/C | 0.0283406 | 0.115616 | intron-variant | AMFR | GRCh38.p7 | 16:56418353 | TACTAAAAATACAAA[A/C]ATTAGCCAGGGGTGG | 267 |
rs141446296 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMFR | GRCh38.p7 | 16:56379813 | CGCTGATGCAAGAGA[C/T]GGGTTTCCGTGGTCT | 267 |
rs141520381 | snp | A/C | 5.38692e-05 | 0.00518957 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362224 | CATGAGATGCAGGAG[A/C]ACCAGAGTTCACGGA | 267 |
rs141527672 | snp | A/G | 0.140919 | 0.224948 | intron-variant | AMFR | GRCh38.p7 | 16:56398295 | ATATGTAAATGTATC[A/G]TTTATATATATAAAT | 267 |
rs141577852 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant, utr-variant-5-prime | AMFR | GRCh38.p7 | 16:56424151 | GATCTGATCAGTCTG[A/C]AATTATCTGTTCTAA | 267 |
rs141685699 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMFR | GRCh38.p7 | 16:56393919 | ACATTCTTCTCACCA[C/T]CACACCACACCTATT | 267 |
rs141758161 | in-del | -/TG | | | intron-variant | AMFR | GRCh38.p7 | 16:56381906 | GATAATGGGGAAGGC[-/TG]TGTGTGTGTGGGCAC | 267 |
rs141766081 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56375543 | AAAGAAAACCAAGAC[A/C]TAACTGAATGTTGTT | 267 |
rs141817821 | snp | A/G | 0.139564 | 0.224285 | intron-variant | AMFR | GRCh38.p7 | 16:56398253 | ATATGTAACTGTATC[A/G]TTTATATATGTAACT | 267 |
rs141822024 | snp | C/G | 1.75799e-05 | 0.00296474 | missense | AMFR | GRCh38.p7 | 16:56363039 | GCATCATCTTCAGAA[C/G]TTTTGTTCAAGAAAC | 267 |
rs141829089 | in-del | -/ACACAC | | | intron-variant | AMFR | GRCh38.p7 | 16:56384704 | CACACATGCATACAT[-/ACACAC]ACACACACACACACA | 267 |
rs141875066 | snp | G/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56413901 | TGGCTACACTGAATA[G/T]GGACTGTGGATTAGA | 267 |
rs141943682 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMFR | GRCh38.p7 | 16:56388020 | TCTATCTCTATCCAT[C/T]CATCCATCCATCCCA | 267 |
rs141944702 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | AMFR | GRCh38.p7 | 16:56381473 | CTTAAGTAGGTGAAC[A/G]AATTAACAAATTGTG | 267 |
rs142068800 | snp | C/T | 1.64746e-05 | 0.00287002 | synonymous-codon | AMFR | GRCh38.p7 | 16:56369247 | ATTGTCTGTTGTTAT[C/T]TCAACTGAGCGTGTC | 267 |
rs142104040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56415789 | CATGGTGGCTCACAC[C/T]TGTAATCCTGGCACT | 267 |
rs142197069 | snp | C/T | 5.20323e-05 | 0.00510034 | synonymous-codon | AMFR | GRCh38.p7 | 16:56385988 | GTGCATCACTTCAAC[C/T]GAAAAACTCGGCAGC | 267 |
rs142213102 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56383630 | TCAAACTCAGCAAGG[A/C]AGCTTCCATTCAGCC | 267 |
rs142226634 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | AMFR | GRCh38.p7 | 16:56390755 | ATGTAAGATCCTTGC[C/G]TTCCAATAATGCTAC | 267 |
rs142231581 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56417744 | ATTTGGGTCCCATCC[C/T]CAAAATATTTCATTA | 267 |
rs142288216 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56373329 | AAAGCTGCACCGACC[A/G]GAGGGAACTCCAGTC | 267 |
rs142350016 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | AMFR | GRCh38.p7 | 16:56365278 | CTGGCAGGAGCCAAT[A/G]AAATACAGGGCCAGG | 267 |
rs142368069 | in-del | -/T | 0.0232847 | 0.105357 | intron-variant | AMFR | GRCh38.p7 | 16:56384545 | GCAGGACTAAGGTGG[-/T]TTTGCACTGGATTTC | 267 |
rs142380616 | snp | A/G | 0.000120947 | 0.00777554 | intron-variant | AMFR | GRCh38.p7 | 16:56403155 | ACACACGGTAAAAGC[A/G]AACGTGAACTTGCTA | 267 |
rs142548887 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | AMFR | GRCh38.p7 | 16:56381350 | AGTCAAACCATATCA[A/G]CATTTAACCAAGGAA | 267 |
rs142596359 | snp | G/T | 0.000791619 | 0.0198792 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362835 | TTTTCCATGGAGCGG[G/T]CAGAATTGGGACAGG | 267 |
rs142629388 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56398366 | TATCATTATATGATA[C/T]ACTATGCTGCACTCC | 267 |
rs142642975 | in-del | -/A | 0.275464 | 0.2487 | intron-variant | AMFR | GRCh38.p7 | 16:56399035 | CTAATGGTAAATTTT[-/A]TGTTATATTTTACCA | 267 |
rs142698336 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56426219 | TAACAATCAAAAGAT[G/T]GGAACAACGCTAATG | 267 |
rs142732254 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56389631 | CATCTACCAAGCTCC[A/T]CGTTGTGACCCCTCT | 267 |
rs142764660 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56383009 | TCAAAAACCTTAAAC[A/G]AACGAAAACACTTCC | 267 |
rs142789897 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | AMFR | GRCh38.p7 | 16:56380021 | TAGCAGGCATTCTGC[A/G]TAGGGGCTCTGATCC | 267 |
rs142820061 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | AMFR | GRCh38.p7 | 16:56376461 | AACAGTAAGAAAACC[A/G]GAAAATCCCAAAATA | 267 |
rs142836436 | snp | A/G | 6.60153e-05 | 0.00574485 | missense | AMFR | GRCh38.p7 | 16:56405003 | CCCTTTCCTTCCCAC[A/G]TCCCTTCGTGGTTGA | 267 |
rs143023320 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | AMFR | GRCh38.p7 | 16:56419082 | GGGCTGGACTGCAGC[A/G]GCGCATTCTTGGCTC | 267 |
rs143050632 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56406951 | CTAAAGCAAATAAGT[C/T]AGTGTAAATGGATTT | 267 |
rs143083640 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56404419 | GCAGATCTACGACAC[C/T]GTAACGTCTAACATA | 267 |
rs143239220 | snp | A/C | 0.122758 | 0.215196 | intron-variant | AMFR | GRCh38.p7 | 16:56392863 | CAGGAAATACAGAGA[A/C]TGCCACAAAGATACT | 267 |
rs143281427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56418343 | ACCCCATCTCTACTA[A/G]AAATACAAAAATTAG | 267 |
rs143293678 | in-del | -/AAAAAAACC | | | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56426358 | CTAAGTCAAAGAAGA[-/AAAAAAACC]CAGCCACAAAGGTCC | 267 |
rs143366684 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56401505 | ACCATACCCAGAAAC[C/T]AAGATGGCAAACTAT | 267 |
rs143395010 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | AMFR | GRCh38.p7 | 16:56363109 | AGATGGGGAGCTGTG[C/G]AACACAGCCAGAAGG | 267 |
rs143453797 | in-del | -/ATTCTCCTGTATC | | | intron-variant | AMFR | GRCh38.p7 | 16:56416550 | TTCCAGGTTCAAGCT[-/ATTCTCCTGTATC]AGCCTCCCAAGTAGC | 267 |
rs143466317 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | AMFR | GRCh38.p7 | 16:56375341 | GGAGAAAAATGGAAT[G/T]CTATAAAATGTTCAG | 267 |
rs143471333 | snp | C/T | 0.000153988 | 0.00877328 | missense | AMFR | GRCh38.p7 | 16:56409533 | TGGACATTCAGCACA[C/T]CAAAGATGAAAATGA | 267 |
rs143493289 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56424978 | GCCCTCGGGGGTCCC[A/T]GGCGGAGGGGCCCCT | 267 |
rs143596271 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56413338 | ACCAGCCCGGCCAAC[A/G]TGGCGAAATCCTGTC | 267 |
rs143666356 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | AMFR | GRCh38.p7 | 16:56409126 | AGACCAGATTTTATT[A/G]TTTATGTATCAAGGT | 267 |
rs143696871 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | AMFR | GRCh38.p7 | 16:56382288 | AAAATGACAAATATT[A/G]TAGAATTCTACTTAT | 267 |
rs143790405 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | AMFR | GRCh38.p7 | 16:56369724 | CTCATATGTTTATTG[A/C]AGCGCTATTCACAGT | 267 |
rs143810379 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMFR | GRCh38.p7 | 16:56387941 | TTTACTCCTCCACCC[C/T]CCTGCCCCACCCTGC | 267 |
rs143845406 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56377942 | GATAAATGATATCAA[C/T]GAAGAATGAAATAAA | 267 |
rs143898784 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56372957 | CGCCACTGCACTCCA[A/G]CCTGGCGACAGAGCA | 267 |
rs143965156 | snp | C/T | 0.287867 | 0.247116 | intron-variant | AMFR | GRCh38.p7 | 16:56397282 | TGGAACCAACCCACA[C/T]GTCCAACAATGACAG | 267 |
rs144029757 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | AMFR | GRCh38.p7 | 16:56406446 | ATGGTGGTTCATGCC[G/T]GTGGTCCCAGCTACT | 267 |
rs144165132 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | AMFR | GRCh38.p7 | 16:56398805 | AAAATAGCAAACTAA[A/C]CCCAAAGCCAACAGA | 267 |
rs144208703 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56410554 | TAAAGATGGACACTG[A/C]AACTGTTTTAAAATT | 267 |
rs144259328 | in-del | -/C | | | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56425844 | GCCGTCGGCCACTTG[-/C]CCCCCCCCCCACCCC | 267 |
rs144278657 | snp | A/C | 0.00755907 | 0.0610114 | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56427078 | TGCCTAATATTCTAA[A/C]AGTCTATTAACTAGA | 267 |
rs144323704 | snp | C/T | 0.000338599 | 0.0130071 | missense | AMFR | GRCh38.p7 | 16:56408076 | AACAGGGACAGGACT[C/T]GACCGTGGCTGCTCA | 267 |
rs144358339 | snp | C/T | 0.000646294 | 0.0179647 | missense | AMFR | GRCh38.p7 | 16:56364098 | AGGTCCAGTGGCACA[C/T]GCTCGGTCTGGACAC | 267 |
rs144396200 | in-del | -/GGTTTTTT | | | downstream-variant-500B | AMFR | GRCh38.p7 | 16:56361044 | ACTGTGATATGGCTG[-/GGTTTTTT]TTTTGTAATGTGTCA | 267 |
rs144509201 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | AMFR | GRCh38.p7 | 16:56415027 | GAAGGAAAAGAAAAC[C/T]GGCGAGAGGGGCCAA | 267 |
rs144519988 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | AMFR | GRCh38.p7 | 16:56373475 | CTTCTTTCCCTCCCC[C/T]GACACCTACATCACG | 267 |
rs144521662 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | AMFR | GRCh38.p7 | 16:56404243 | TACTTTCTTTAAAAA[C/G]TATGTTTTCAAAGTT | 267 |
rs144635686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56366106 | ACTGGAGGCCGGGCG[C/T]GGTGGCTCACGCCTG | 267 |
rs144641410 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | AMFR | GRCh38.p7 | 16:56374461 | TCAAATTATAGAGAA[C/T]CAAAGATTAAGAAAA | 267 |
rs144679769 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | AMFR | GRCh38.p7 | 16:56371978 | TATATGGAAGATGTG[C/T]GCAGGTTATATACAA | 267 |
rs144765742 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | AMFR | GRCh38.p7 | 16:56380535 | CTATCGCATTGTCAA[A/G]CTGCAAATTTTCCAA | 267 |
rs144875386 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | AMFR | GRCh38.p7 | 16:56378535 | ATAAATAACCTAGGG[C/T]ATGGCAATGACTTTT | 267 |
rs145000724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56421547 | GAGTTCTATTTAAAT[A/G]ATATTATTTGCATAA | 267 |
rs145006018 | in-del | -/ATA | | | intron-variant | AMFR | GRCh38.p7 | 16:56402345 | TCCAAAATAATAATA[-/ATA]ATAATAATAATGGCT | 267 |
rs145063914 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | AMFR | GRCh38.p7 | 16:56386899 | GTCAGGAGATCAAGA[C/T]CATCTTAGCCAAAAT | 267 |
rs145076618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56417236 | CCAACATAGTGAAAC[C/T]CCATCTCCACAAAAG | 267 |
rs145090014 | in-del | -/CT | 0.111224 | 0.207945 | intron-variant | AMFR | GRCh38.p7 | 16:56387995 | AAATGCCTGGAACCC[-/CT]CTGTTTGTTCTATCT | 267 |
rs145091841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56390279 | AAGAATGAAATGGCT[A/G]GATGAATTAATCTCC | 267 |
rs145158969 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56423199 | GAAACTACATATACA[C/T]TGAGTGATGAGACAA | 267 |
rs145353118 | in-del | -/A | | | intron-variant, upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56424372 | AGCAGAAAAGGAAGC[-/A]CAGTTTGGTGTTTGT | 267 |
rs145363453 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56402113 | GAGGCCGAGGTAGGG[A/G]GATCATGAGGTCAGG | 267 |
rs145391865 | snp | C/T | 0.0157543 | 0.0873438 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362489 | GATGTTACCCCACGA[C/T]GTGGGGGCGGGCTCA | 267 |
rs145426287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56400436 | CCGCTGCAGCCATTA[C/T]TAACCAATCCCCCTG | 267 |
rs145447404 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56412584 | AAGCATTTAAGCCAG[C/T]AGAAGTGGCTCACAC | 267 |
rs145457790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56368238 | ATTACTGGCCACCCT[C/T]CCTTCCCCAGCTCAC | 267 |
rs145612255 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | AMFR | GRCh38.p7 | 16:56418580 | TTTGGGAGGCCGAGG[C/T]GGGCGGATCACGAGG | 267 |
rs145641153 | snp | A/T | 0.0283406 | 0.115616 | intron-variant | AMFR | GRCh38.p7 | 16:56400262 | TACCTCAGCCTCCCA[A/T]GTACCTGGGATTACA | 267 |
rs145705407 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | AMFR | GRCh38.p7 | 16:56422334 | TTTACAAGTACCCCA[C/G]ATGACCACATACCAG | 267 |
rs145747194 | snp | A/G | 3.40049e-05 | 0.00412326 | missense | AMFR | GRCh38.p7 | 16:56362938 | GCTTCTGAAGCCTCC[A/G]TTCCGCGGCGGCAGC | 267 |
rs145795496 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56406278 | GTATTTTTTTTATTA[C/T]AGAAATTGACGGCCA | 267 |
rs145884033 | snp | C/T | 1.65143e-05 | 0.00287348 | synonymous-codon | AMFR | GRCh38.p7 | 16:56369196 | GCCCAGTTTTACCTG[C/T]GTAGGAAAAGGTACT | 267 |
rs145909782 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | AMFR | GRCh38.p7 | 16:56413565 | ACTCAAATCCTCAGC[A/G]AACTGCCAATCTATA | 267 |
rs145910599 | in-del | -/C | 0.0283406 | 0.115616 | intron-variant | AMFR | GRCh38.p7 | 16:56378753 | TTAACAATAAAAAAA[-/C]AAACAACCTGATCAA | 267 |
rs145952056 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | AMFR | GRCh38.p7 | 16:56365312 | GCTGTGACGGGAGCA[C/T]GTTCACCTTCCACTG | 267 |
rs146109122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56415099 | CCTTCTTCAACAGTC[C/T]ATGAGAAAACTTGAA | 267 |
rs146110950 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | AMFR | GRCh38.p7 | 16:56378701 | GACACATCTGATAAA[A/G]GACTGCTATCCAAAA | 267 |
rs146151347 | snp | A/T | 0.0228947 | 0.104514 | intron-variant | AMFR | GRCh38.p7 | 16:56380140 | CCATACATCTTCTGA[A/T]ATCTAGGCGGAGGTT | 267 |
rs146158681 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | AMFR | GRCh38.p7 | 16:56377844 | TTTGAAATTAAAAGC[A/G]CAGTATGCTTTATAT | 267 |
rs146162168 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | AMFR | GRCh38.p7 | 16:56419085 | CTGGACTGCAGCGGC[A/G]CATTCTTGGCTCACT | 267 |
rs146197707 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56375835 | AGGTCGAGAAGGGCA[G/T]ATCACTTGAGGTCAA | 267 |
rs146197782 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | AMFR | GRCh38.p7 | 16:56417997 | GCAAAACCCCATCTC[C/T]ACTAAAAACACAACA | 267 |
rs146293237 | snp | C/T | 3.39593e-05 | 0.0041205 | synonymous-codon | AMFR | GRCh38.p7 | 16:56385949 | GGAGTTGCTGGCCTG[C/T]GTAATGCCAAGAATG | 267 |
rs146390289 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | AMFR | GRCh38.p7 | 16:56414697 | GGTCCTTCCCAAGTA[C/T]CTCATTTCCGACATT | 267 |
rs146401111 | snp | A/C | 0.030665 | 0.119967 | intron-variant | AMFR | GRCh38.p7 | 16:56410743 | AAAAATTAGCTGAGC[A/C]TGGTGGCACAAGCCT | 267 |
rs146451278 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | AMFR | GRCh38.p7 | 16:56371097 | TGTTTATGTAAACAT[A/G]AGTTGATCATTATTT | 267 |
rs146452555 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | AMFR | GRCh38.p7 | 16:56411597 | CTACAAATTAACAAC[A/G]TGACTCCTTAAAGAT | 267 |
rs146463784 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56406801 | GTATATACTATAGTA[C/T]GAGCTGACGGGCCTA | 267 |
rs146593750 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | AMFR | GRCh38.p7 | 16:56373926 | TAATCCCAGCACTTC[A/G]GGAGGTCAAGGCAGG | 267 |
rs146702495 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56374682 | ACAAAGACTGCCTCC[A/C/G]ACAAACCAAAGTTGG | 267 |
rs146727253 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56386268 | CCCTTGGTCTTTGGT[C/G]TCTGAGGCACTTAGA | 267 |
rs146760876 | in-del | -/CT | 0.256619 | 0.249912 | intron-variant | AMFR | GRCh38.p7 | 16:56419056 | TTAGACAGAGTCTCA[-/CT]CTGTCGCCCGGGCTG | 267 |
rs146826823 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | AMFR | GRCh38.p7 | 16:56391614 | ATGCCCACGGAGCCT[C/T]GCTCGTTGCTAGCAC | 267 |
rs146897753 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | AMFR | GRCh38.p7 | 16:56396771 | ATGGGAGAAAATTTT[C/T]GCAATCTACTCATCT | 267 |
rs146995844 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | AMFR | GRCh38.p7 | 16:56379439 | GACACAGTCAAACCA[C/T]ATCATTCCGCCCCGG | 267 |
rs147076844 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | AMFR | GRCh38.p7 | 16:56397119 | TGGAAGACAATGTGG[C/T]GATTCCTCAGGGATC | 267 |
rs147118948 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56398263 | GTATCATTTATATAT[A/G]TAACTGTATCATTTA | 267 |
rs147150330 | in-del | -/TT | | | intron-variant | AMFR | GRCh38.p7 | 16:56379910 | TTGAGTGTCTGTGGC[-/TT]TTTTCCAGGCACACA | 267 |
rs147173570 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56424983 | CGGGGGTCCCTGGCG[G/T]AGGGGCCCCTAGGCC | 267 |
rs147181762 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | AMFR | GRCh38.p7 | 16:56372780 | CACTTGAGGTCAGGA[A/G]TTAGAGACCATCCTT | 267 |
rs147268298 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | AMFR | GRCh38.p7 | 16:56376847 | AATAGATAAGCCTCT[A/T]AGCCAAGCTAACTAC | 267 |
rs147276641 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56373037 | TGGAGGAAAACCTGA[C/G]TTATAACTGACAAAT | 267 |
rs147373854 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | AMFR | GRCh38.p7 | 16:56393578 | TCTCTGACAAAACAG[A/C]CTTTAAACCAACAAT | 267 |
rs147383661 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMFR | GRCh38.p7 | 16:56389735 | TGAATCATCCAACAC[C/T]CTGGCCTCTCATGTC | 267 |
rs147481249 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | AMFR | GRCh38.p7 | 16:56409236 | AAGAAAGCTCCCCAG[A/G]AGACAACGATTCTGC | 267 |
rs147482147 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56366940 | GAAAGCCATGTTTTC[C/G]CCCCAGCCCCACTCA | 267 |
rs147563238 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | AMFR | GRCh38.p7 | 16:56417722 | AACAGAGGAATTTCA[C/T]GTTTACATTTGGGTC | 267 |
rs147623294 | snp | A/G | 0.000115579 | 0.00760107 | synonymous-codon | AMFR | GRCh38.p7 | 16:56407997 | CAAGGTGTGCATTCC[A/G]TGGGTGTAGCCGGTG | 267 |
rs147655118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56368385 | GAGAACTGGGAACCA[C/T]ATCTAATATCTCAGC | 267 |
rs147742512 | snp | C/T | 0.000141962 | 0.00842383 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362684 | AAGAGATCATACCTA[C/T]AGTTAAAATTTGCAG | 267 |
rs147760524 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | AMFR | GRCh38.p7 | 16:56385306 | ATCATTCACTCCAGC[C/T]GATAATTCCCCAACA | 267 |
rs147760918 | snp | A/G | 7.29195e-05 | 0.00603775 | missense | AMFR | GRCh38.p7 | 16:56408106 | ATCGGCGTGGTGGGC[A/G]AGAAGGAAAGCTGAA | 267 |
rs147816556 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56418066 | GCTACTTGGGAGGCT[A/G]AGGTGGGAGAATCAC | 267 |
rs147868368 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | AMFR | GRCh38.p7 | 16:56400063 | ACTTTCCCTCGGCCG[G/T]TCTGGCATCACACCC | 267 |
rs147939986 | in-del | -/GT | | | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56361785 | AAAAAAAAAAAAAAA[-/GT]AATCCAATGGGGCAT | 267 |
rs147982664 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | AMFR | GRCh38.p7 | 16:56375513 | TGCCAAGTAAGAGAG[C/G]TTGTCAGAGTAAATA | 267 |
rs148034591 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56379587 | AAGGCAAGTCCCTAA[C/T]GTCTATGAGCCTGTA | 267 |
rs148125206 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56382451 | CCTGGGCCACACTGG[A/G]AGAAGAATTGTCTTG | 267 |
rs148164236 | snp | A/G | 1.65061e-05 | 0.00287277 | missense | AMFR | GRCh38.p7 | 16:56414283 | CGAAGAGGGCCAAAC[A/G]CAATACACTGGATGA | 267 |
rs148177825 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | AMFR | GRCh38.p7 | 16:56387947 | CCTCCACCCTCCTGC[C/G]CCACCCTGCCCATAT | 267 |
rs148188171 | snp | C/T | 0.029116 | 0.117091 | intron-variant | AMFR | GRCh38.p7 | 16:56397374 | TGAGTTCATGTCCTT[C/T]GTAGGGACATGGATG | 267 |
rs148220554 | in-del | -/T | 0.0150606 | 0.0854603 | intron-variant | AMFR | GRCh38.p7 | 16:56388920 | CTGCTTTACAGTAAA[-/T]TTTTTTTTGTATGTA | 267 |
rs148343613 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AMFR | GRCh38.p7 | 16:56363450 | ACCATGGGTGTGTGA[C/T]GCACAGATGCGCTGA | 267 |
rs148417005 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | AMFR | GRCh38.p7 | 16:56419373 | ATCTATTTTTTAAAA[A/T]TTTTTTAAAGTTTAG | 267 |
rs148468859 | snp | C/T | | | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56426203 | AATGTTGATTACATT[C/T]TAACAATCAAAAGAT | 267 |
rs148522129 | in-del | -/AAG | | | intron-variant | AMFR | GRCh38.p7 | 16:56374810 | AAAGGAAGAGCATCA[-/AAG]AAGGTATAAATAAAT | 267 |
rs148564295 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56381070 | AGAAAGAGGTTTAAT[A/G]GACTTACAGTTCCAC | 267 |
rs148658139 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | AMFR | GRCh38.p7 | 16:56398939 | TTCATAAGACAAAAA[A/T]GTTCTGGAGATAGAT | 267 |
rs148721236 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | AMFR | GRCh38.p7 | 16:56410575 | TTTTAAAATTTTCAC[C/T]ACGCAAAAAAAACAT | 267 |
rs148776965 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | AMFR | GRCh38.p7 | 16:56415697 | TCAAACAACCAGGAA[C/G]AAACGCCCAAACTAG | 267 |
rs148822453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56374987 | TTAGGATTGTTTTGT[C/T]ATCAAAAGGTACTCA | 267 |
rs148883836 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56418189 | AAAAAAAAAAACTGC[A/T]TAAAAAAAGTAAACT | 267 |
rs148942872 | snp | A/C | 0.0356815 | 0.128715 | intron-variant | AMFR | GRCh38.p7 | 16:56395495 | CCCTTCATTCTAAAA[A/C]CTCTCAATAAATTAG | 267 |
rs148975651 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56369639 | TTTTAACTACCATTC[A/G]AACCAGCAATCCCAC | 267 |
rs149039018 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | AMFR | GRCh38.p7 | 16:56378599 | AAAATAATTGATAAG[C/T]TGGACTTCATTAAAT | 267 |
rs149090863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56382262 | TATGCTAAGTGAAAT[A/G]AGCCAGTCACAAAAT | 267 |
rs149133755 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56398185 | TTTATATATATAACT[C/G]TATCATTTATATATA | 267 |
rs149175278 | in-del | -/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56420555 | AAGACATTCCTTTTA[-/T]TTTTTAATTTATCTA | 267 |
rs149189412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56400976 | TATGTGTTGAGTTAC[C/T]GAGACTCTAGCTCCC | 267 |
rs149207259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56392162 | GAGGGTCCTGACTGT[C/T]AGGAGGAAAACTAAC | 267 |
rs149296126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56403591 | ATATAACTATCTTTA[C/T]CAAACTAATACATGA | 267 |
rs149312321 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | AMFR | GRCh38.p7 | 16:56366100 | TCAAAAACTGGAGGC[C/T]GGGCGCGGTGGCTCA | 267 |
rs149359659 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | AMFR | GRCh38.p7 | 16:56414534 | TTAGGGATGAGGACC[A/G]GAAAGAGAGGCACCA | 267 |
rs149475445 | snp | G/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56397240 | CACGTTATGTTTATT[G/T]TGGCACTACTCACAA | 267 |
rs149507254 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | AMFR | GRCh38.p7 | 16:56372723 | TGACACAGTGGCTCA[C/T]GCCTGTAATCCCAGC | 267 |
rs149589472 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | AMFR | GRCh38.p7 | 16:56410485 | TTGTATTGTTAGAAC[A/C]TTAACAATGTCAATG | 267 |
rs149614022 | snp | C/T | 3.33728e-05 | 0.00408476 | missense | AMFR | GRCh38.p7 | 16:56364048 | GCTCCACTTCCACCT[C/T]GCCGAAGTCCAGCGT | 267 |
rs149623671 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56384780 | GATGGGGAACAAAAA[A/C]ACACATTTGGTGAGC | 267 |
rs149694548 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | AMFR | GRCh38.p7 | 16:56412311 | CAGGGAAGATGCGAT[C/T]GATGCTGAAAAAAAT | 267 |
rs149788614 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | AMFR | GRCh38.p7 | 16:56361195 | AGTAAAATAATCTTT[C/T]GCTACACACTTACCT | 267 |
rs149842588 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | AMFR | GRCh38.p7 | 16:56368801 | AGTCTTGCTTATTTA[C/T]TTAAATACTATCCAT | 267 |
rs149854485 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | AMFR | GRCh38.p7 | 16:56405943 | CAGTAAGCAGAGATC[A/G]CACCACAGCACTCCA | 267 |
rs149886732 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56389959 | CAGCCGTACAGGTCC[A/T]TACCTCCCTGTTCCC | 267 |
rs149907603 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | AMFR | GRCh38.p7 | 16:56378419 | TGCAAAACAATAATC[C/T]AGACACAGCCCTTAT | 267 |
rs149927445 | snp | C/T | 0.000742372 | 0.0192519 | missense | AMFR | GRCh38.p7 | 16:56405010 | CTTCCCACGTCCCTT[C/T]GTGGTTGAGGTCCCA | 267 |
rs150153744 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | AMFR | GRCh38.p7 | 16:56386258 | AGCACTAGTACCCTT[A/G]GTCTTTGGTCTCTGA | 267 |
rs150162342 | snp | A/T | 0.00122284 | 0.0246966 | intron-variant | AMFR | GRCh38.p7 | 16:56403163 | TAAAAGCGAACGTGA[A/T]CTTGCTAGTGATGAA | 267 |
rs150244606 | in-del | -/C | 0.0107246 | 0.0724382 | intron-variant | AMFR | GRCh38.p7 | 16:56369921 | ACAGAAACTCAAATA[-/C]CGTATGTTCTTATAA | 267 |
rs150319609 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | AMFR | GRCh38.p7 | 16:56364733 | TGTGACCACAGGCTC[A/G]TGCCACCACATCTGG | 267 |
rs150361693 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | AMFR | GRCh38.p7 | 16:56421510 | TTTATCCACTTTTGT[A/T]TGTGGTCATTTTTCC | 267 |
rs150382887 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | AMFR | GRCh38.p7 | 16:56408305 | GATATTTAGAGATCC[A/G]TGTCATTTAATTTAC | 267 |
rs150415040 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56391970 | GGCACCCCCCAGTAA[A/G]GGCAGACTGACACTT | 267 |
rs150499616 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | AMFR | GRCh38.p7 | 16:56394216 | TTTAAGGCAGTGTGT[A/G]GAGGGAAATTTATAG | 267 |
rs150646468 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | AMFR | GRCh38.p7 | 16:56414486 | GCAAGATAAGGAATA[C/T]CTGAAAAGGCACACT | 267 |
rs150654710 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | AMFR | GRCh38.p7 | 16:56388479 | TTATAAACACTGTAC[A/G]CTTAGGCTACACTAA | 267 |
rs150768397 | in-del | -/TAAT | 0.0178098 | 0.0926698 | intron-variant | AMFR | GRCh38.p7 | 16:56399441 | GATGAATGGATAAAC[-/TAAT]TGTTTAATTTATAAA | 267 |
rs150798359 | snp | C/T | 1.64958e-05 | 0.00287187 | missense | AMFR | GRCh38.p7 | 16:56401760 | TGTCCACAGGGCAGT[C/T]TCCGCGCAGCCTGCA | 267 |
rs150867127 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, utr-variant-5-prime | AMFR | GRCh38.p7 | 16:56424171 | ATCTGTTCTAATGAA[C/T]GAAACCAGCATGTGT | 267 |
rs150894119 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56409687 | TATGGAAGATATATT[C/T]TGCACTTGGCTTTCT | 267 |
rs150911013 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | AMFR | GRCh38.p7 | 16:56384372 | TCTACCTTAATGACA[C/T]TGCAGGTGCTATGCT | 267 |
rs150974469 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56426252 | CGTCAAGCGATGAGT[C/G]GATAAATGTGATACA | 267 |
rs151027201 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | AMFR | GRCh38.p7 | 16:56396658 | ACACCAAAAGCAATG[G/T]CAACCAAAGCCAAAA | 267 |
rs151116051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56405601 | GTAACTCCAAGTATA[A/G]TTCAGGTACTGCTAT | 267 |
rs151169131 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56377966 | AAATAAACGAAGAGA[C/T]AGTCCATGTTCATGG | 267 |
rs151179213 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | AMFR | GRCh38.p7 | 16:56416389 | TCACACACATCTTAA[C/G]TTATCAAATAAAAAA | 267 |
rs151230665 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | AMFR | GRCh38.p7 | 16:56420485 | ATAGACGAGAGTCCG[C/G]ACGCAAAGCATACCT | 267 |
rs151301190 | snp | C/G/T | 3.30062e-05 | 0.00406229 | missense | AMFR | GRCh38.p7 | 16:56401780 | CGCAGCCTGCATGGA[C/G/T]TCCCAACAGATGGCA | 267 |
rs151325604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56373415 | TCACAGTCCAGAGCA[C/T]GGGCTCACTAAAAGA | 267 |
rs180778962 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56411835 | CTGTTTCCAGACCTG[A/G]TGCAGGGAAAGTACA | 267 |
rs180782429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56395688 | TGGCCAGGGCAATCA[A/G]GCAGGAGAAAGAAAT | 267 |
rs180792693 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56367026 | TGACAAGTGAGGTGT[C/G]GGGGAGGGCATCTCA | 267 |
rs180795943 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | AMFR | GRCh38.p7 | 16:56384930 | CCTCAGCCTCCCAAG[C/T]AGCTGGGATTACAGG | 267 |
rs180818964 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56374742 | GAAATGTTAAAAATA[C/T]TAAGTCGTTTAAAGA | 267 |
rs180950974 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | AMFR | GRCh38.p7 | 16:56423706 | CAGATTTGAAATTAA[C/G]CAAGAGATGTGAGTT | 267 |
rs180985490 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56402165 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATG | 267 |
rs181094007 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | AMFR | GRCh38.p7 | 16:56366175 | TGAGGTCAGGAGATC[A/G]AGACCATCCTGGCTA | 267 |
rs181120527 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AMFR | GRCh38.p7 | 16:56396007 | TTCAAGGAGAACTAC[A/G]AACTAATGCTCAACA | 267 |
rs181123059 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | AMFR | GRCh38.p7 | 16:56413331 | GTTTGAGACCAGCCC[A/G]GCCAACGTGGCGAAA | 267 |
rs181152281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56375647 | ACCAAAAGAAACCAG[A/G]AGCAGCTATATTACT | 267 |
rs181155946 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56422183 | AAGGTCAAGGTTACA[C/T]GACATCACACTCTAG | 267 |
rs181159810 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | AMFR | GRCh38.p7 | 16:56399919 | CTAGCCTCCAAGCTC[C/T]TTAGGGGCTAACTAA | 267 |
rs181294366 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | AMFR | GRCh38.p7 | 16:56361173 | AAGTATAATGTAATT[C/T]GAGGACAGTAAAATA | 267 |
rs181386094 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56378209 | TTACAAAGCAACAGT[A/G]ATCAAGACAATGCGG | 267 |
rs181391948 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | AMFR | GRCh38.p7 | 16:56408484 | TCTGTTTCTTTCTCA[A/G]TCTTGCTCTAGTCCT | 267 |
rs181430267 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | AMFR | GRCh38.p7 | 16:56391559 | GATTATATCCTGCGT[A/G]TGGCTCGGAGGGTCC | 267 |
rs181434992 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56416733 | AGGCATGAGCCACTG[C/T]GCCCAGCCTAAATAA | 267 |
rs181436385 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56370822 | ATTCAAGGTTTTATT[C/T]TTGGAAAAGTTCTAA | 267 |
rs181443013 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | AMFR | GRCh38.p7 | 16:56398098 | TTATAATATATAAAT[C/G]TATCATTTATAATAT | 267 |
rs181481492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56369783 | CCTTCAACACAGGAT[C/T]TGATAAAGAAAATGA | 267 |
rs181490715 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362086 | AACCCACAGGCTTTA[A/G]CACTGCCTAATTTAC | 267 |
rs181646244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56378801 | TTAATAGATACTTCA[C/T]CAAAGATAGATGTAC | 267 |
rs181653421 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AMFR | GRCh38.p7 | 16:56416839 | CCCATCACCCATAGA[A/G]CAACCACTTCCTATT | 267 |
rs181727470 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56417162 | CACCTATAATCCCAG[A/C]ACTTTCGGAGGCCAA | 267 |
rs181739858 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56379267 | GCAAAGAGAGAGAGC[G/T]TGTGCAGGTGAACTC | 267 |
rs181753291 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56398140 | ATTTATAATATATAA[A/C]TCTATCATTTATAAT | 267 |
rs181942823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56408185 | TTCACTGAGAAATTC[A/G]AGGTCAATCTTGGCT | 267 |
rs181957733 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMFR | GRCh38.p7 | 16:56370287 | AATTCAAATACATCA[C/T]GTTAGGTGAAAGAGG | 267 |
rs182001894 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56422936 | GATAAGTTTTGGGAA[A/T]TACAATATGTTAATA | 267 |
rs182023862 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56384398 | ATGCTCACTACAGTG[A/C]CTGTCTCAGGAACAG | 267 |
rs182029799 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56366246 | AGCCAGGCGTGGTGG[C/T]GGGCGCCTGTAGTCC | 267 |
rs182031104 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56401345 | CTTTTGGGCATGTAC[A/C]AAATGCAAAATTATA | 267 |
rs182255818 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56391163 | TTTGTTCACTCAACC[C/T]GAGGCAGATAAGTGT | 267 |
rs182266269 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56376895 | CCTAAATTACTAATA[C/T]AAGAAATATTATACA | 267 |
rs182276000 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56413870 | AACAGCTATAAAAAA[C/T]AATATTGGGACAACT | 267 |
rs182277427 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | AMFR | GRCh38.p7 | 16:56397166 | ATTTGACCCAGCCAT[C/T]CCATTACTGGGTATA | 267 |
rs182503958 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | AMFR | GRCh38.p7 | 16:56402803 | TAGAGGTGAAGTAAA[C/T]TGCCCCAAATCACAC | 267 |
rs182520966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56367801 | ACAACAAAAACAATG[A/G]TAACAGCAGAGAACA | 267 |
rs182529055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56385847 | CAAGGTCATATACCC[A/G]GCACACACGCTCTAG | 267 |
rs182638740 | snp | C/T | 0.0248432 | 0.108648 | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56425722 | ACGGCTTGGCTGGGC[C/T]CGCAGACACAGAGGG | 267 |
rs182648273 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | AMFR | GRCh38.p7 | 16:56372942 | AGTGAGCCAAGATCT[C/T]GCCACTGCACTCCAG | 267 |
rs182655329 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56410335 | CACAACACAACCACT[G/T]GCCAGCCCATAATAA | 267 |
rs182658689 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56394307 | TAAAAGAACTAGAGA[A/T]GCAAGAGCAAACACA | 267 |
rs182775972 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | AMFR | GRCh38.p7 | 16:56377467 | TAGGAATAGAGGGAA[A/T]CTTTGTCACTGTGAT | 267 |
rs182924182 | snp | C/T | 0.000280887 | 0.0118476 | synonymous-codon | AMFR | GRCh38.p7 | 16:56404936 | ATGGTGCATGAGGTC[C/T]AGGGACAGGAGAGTG | 267 |
rs182984194 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56414836 | GAGTGTGGATGGTCA[C/T]AAAAAAGTCTCATCA | 267 |
rs183076390 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | AMFR | GRCh38.p7 | 16:56397612 | CAGCACACCAACATG[G/T]CACATGTATACATAT | 267 |
rs183080576 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, utr-variant-5-prime | AMFR | GRCh38.p7 | 16:56424131 | TCTCTAGCCAAAATA[C/T]CGTTGATCTGATCAG | 267 |
rs183092650 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362626 | GGCGACTGCTCACTT[A/C]CTCCTGATCGTCCCC | 267 |
rs183098171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56364514 | AACCAGTCTTATCCA[A/G]TCTTCTGCACAAATT | 267 |
rs183103772 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | AMFR | GRCh38.p7 | 16:56409180 | GTCTGCATAGGTGAA[C/G]TGACCCCATGTTAGC | 267 |
rs183108874 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56393429 | TGGCAAATTGGATAG[G/T]CAAGACCCATCAGTG | 267 |
rs183112456 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56380022 | AGCAGGCATTCTGCG[C/T]AGGGGCTCTGATCCC | 267 |
rs183170470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56363339 | AGGGTCTGCCAGGGC[C/T]CAAACCCACTTGAGG | 267 |
rs183194248 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56398211 | ATATATAACTCTATC[A/G]TTTATATATATAACT | 267 |
rs183393667 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | AMFR | GRCh38.p7 | 16:56417999 | AAAACCCCATCTCTA[C/T]TAAAAACACAACAAA | 267 |
rs183491358 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56418815 | TCCGTCTCAAAAAAA[A/T]AAAGGAAATATGTGC | 267 |
rs183515502 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56403557 | GGGAAGATAGTACTA[A/G]ATAAATGAAAAAAGC | 267 |
rs183518450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56388288 | ACACAGTGCTAAGTA[C/T]TTGTGTATCTAAACA | 267 |
rs183521639 | snp | A/C | | | intron-variant, upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56424570 | ATCCGCTAACAATCC[A/C]ATGCCTGACCAAGTG | 267 |
rs183582445 | snp | C/T | 0 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56371557 | AGTAGCTGCACTGGG[C/T]GACCACACTCCCAGG | 267 |
rs183657792 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | AMFR | GRCh38.p7 | 16:56410084 | GAGGCTAAGGTGGGA[A/G]GATTGCTTGAGCCCA | 267 |
rs183676590 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AMFR | GRCh38.p7 | 16:56372098 | ATTTTGGTATCTGAA[A/G]GAGGGGGTCCTAGAA | 267 |
rs183826921 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56398084 | TATAAATGTATCATT[A/T]ATAATATATAAATGT | 267 |
rs183835179 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56416516 | AATGGTGCAATCTCC[A/G]CTCACTGCAACCTCG | 267 |
rs183857178 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56377959 | AAGAATGAAATAAAC[A/G]AAGAGATAGTCCATG | 267 |
rs183859371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56393925 | TTCTCACCACCACAC[C/T]ACACCTATTCCAAAA | 267 |
rs183943797 | snp | A/C | 0.00438332 | 0.0466095 | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56426919 | TTACCAAAGGAAAAA[A/C]ATGTTACCTTGGGAG | 267 |
rs183973097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56390276 | CTAAAGAATGAAATG[A/G]CTGGATGAATTAATC | 267 |
rs183979271 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56405375 | TTTACCCATTATTTT[A/C]TTTTCTCTGCTTCAA | 267 |
rs184053374 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56396285 | TGACTTCAAACTATA[A/C]TACAAGGCTACAGTA | 267 |
rs184209963 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | AMFR | GRCh38.p7 | 16:56376011 | TGCAGTGAGCCGAGA[C/T]CGGGCCACTGCACTC | 267 |
rs184210907 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56413667 | CAATCTCACCCAAAA[C/T]AAGAACAAATCTCCT | 267 |
rs184359098 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56383012 | AAAACCTTAAACAAA[C/T]GAAAACACTTCCCTG | 267 |
rs184365579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56410770 | GCCTGTAATCCCAGC[C/T]ACTTGGGAGGCTGAG | 267 |
rs184377576 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56401120 | AAAGATACCTCAAGG[G/T]CCATCAACATCAAAA | 267 |
rs184392550 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | AMFR | GRCh38.p7 | 16:56366239 | AAAAATTAGCCAGGC[A/G]TGGTGGTGGGCGCCT | 267 |
rs184407968 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | AMFR | GRCh38.p7 | 16:56388699 | AAGTTTTAATTTTAC[C/T]TTTTAAATTTTTTTG | 267 |
rs184568725 | snp | C/T | 9.8894e-05 | 0.00703116 | synonymous-codon | AMFR | GRCh38.p7 | 16:56369217 | AAAAGGTACTTGAAT[C/T]CGTCCTTCTAAAATA | 267 |
rs184728827 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | AMFR | GRCh38.p7 | 16:56416734 | GGCATGAGCCACTGC[A/G]CCCAGCCTAAATAAG | 267 |
rs184742244 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56364728 | GTAGCTGTGACCACA[C/G]GCTCGTGCCACCACA | 267 |
rs184805333 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56407547 | CCACCACGCCCAACT[A/G]ATTTTTTTTTTGTAT | 267 |
rs184844099 | snp | A/G | 0.139225 | 0.224118 | intron-variant | AMFR | GRCh38.p7 | 16:56398103 | ATATATAAATGTATC[A/G]TTTATAATATATAAA | 267 |
rs184881046 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56399603 | GAATAGGTTAATCCA[C/T]AGAGACAGAAAGTGG | 267 |
rs184892050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56399130 | AACACTTCACACCCA[C/T]GAGAATGGCTATAAT | 267 |
rs184911251 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56420048 | CAGGAAAATGTCCCT[A/T]CCAGAATGGTTCTAC | 267 |
rs184915913 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | AMFR | GRCh38.p7 | 16:56365588 | GCACAACATGTAGGT[A/T]CATACACACACACGC | 267 |
rs184996904 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56382019 | ACAAACAAAAAAGAC[A/T]CATGAGTATTCAAAA | 267 |
rs184999016 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | AMFR | GRCh38.p7 | 16:56421369 | CTCTGCAACTTCCTT[A/G]ATTTATTTAATTTGT | 267 |
rs185056408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56377847 | GAAATTAAAAGCGCA[A/G]TATGCTTTATATTAG | 267 |
rs185084222 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | AMFR | GRCh38.p7 | 16:56379315 | ATATCTCGTGAGACT[C/T]ATTCACTATCACGAG | 267 |
rs185092260 | snp | A/G | 0.139564 | 0.224285 | intron-variant | AMFR | GRCh38.p7 | 16:56398190 | ATATATAACTCTATC[A/G]TTTATATATATAACT | 267 |
rs185175358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56422331 | CATTTTACAAGTACC[C/T]CAGATGACCACATAC | 267 |
rs185195718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56412418 | AGGTTATACTTTCTA[C/T]AAATTTCAACCTGAT | 267 |
rs185197934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56395864 | AATGTGCAAAAATCA[C/T]AAACATTCTTATACA | 267 |
rs185240897 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | AMFR | GRCh38.p7 | 16:56395090 | TTCACAGCCGAATTC[C/T]ACCAGAGGTACAAGG | 267 |
rs185254860 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56417199 | GGGATTGCTTGAACT[A/C]AGGAGTTCAAGACCA | 267 |
rs185339026 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56373629 | CACAGAGCAGAGATG[C/G]TGAAATTAACAGACT | 267 |
rs185508234 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | AMFR | GRCh38.p7 | 16:56411148 | GGTCTAGTTCCCCCA[A/C]ATGTTAAAATAGACT | 267 |
rs185552671 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56374199 | AAACAGAATAAAAAC[G/T]GAAAATAACAGAGCA | 267 |
rs185632233 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56408543 | TTAGGGCTAGCACAA[A/T]TGAAATGCAATCCAG | 267 |
rs185640193 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | AMFR | GRCh38.p7 | 16:56392443 | GAAGTTTGAACCCAT[C/T]GCAAAGAAGTTAAAA | 267 |
rs185655804 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | AMFR | GRCh38.p7 | 16:56370127 | TGTAAGAAACCTGCA[C/T]TTGTAACCTGTAAAC | 267 |
rs185661597 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56398059 | ATATATAAATGTATC[A/G]TTTATAATATATAAA | 267 |
rs185674725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56370941 | TTCTGACTATAGAAG[A/G]AGCAGGGAGTATGTC | 267 |
rs185680897 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56395554 | AAGAGCTATTTATGA[A/C]AAACCCACAGCCAAC | 267 |
rs185753267 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | AMFR | GRCh38.p7 | 16:56378862 | CCACATCATATGTCA[C/T]TAGATAAATGCAAAT | 267 |
rs185763340 | snp | A/G | 0.139225 | 0.224118 | intron-variant | AMFR | GRCh38.p7 | 16:56398147 | ATATATAACTCTATC[A/G]TTTATAATATATAAC | 267 |
rs185788671 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56416178 | GCAACACATTTAGCA[A/C]TTGTTCGAGGCATGT | 267 |
rs185804957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56390742 | AGATTATAAAAATAT[A/G]TAAGATCCTTGCCTT | 267 |
rs185813925 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | AMFR | GRCh38.p7 | 16:56375042 | TTATCTGAAAATAAA[C/T]GAATTAGTTGCAAAT | 267 |
rs185814350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56402353 | AATAATAATAATAAT[A/G]ATAATGGCTGCTGTT | 267 |
rs185835415 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56367031 | AGTGAGGTGTGGGGG[A/T]GGGCATCTCAATGGC | 267 |
rs185942502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | AMFR | GRCh38.p7 | 16:56423818 | CTGCCTTCTACTAAA[C/T]TCTCCATCAGAAGGA | 267 |
rs185966550 | snp | A/G | 3.35734e-05 | 0.00409702 | synonymous-codon | AMFR | GRCh38.p7 | 16:56362978 | TCGACGCAGGGTCAC[A/G]GGGTCAGAGGACGCA | 267 |
rs185980756 | snp | C/G | 0.0330031 | 0.124146 | intron-variant | AMFR | GRCh38.p7 | 16:56385407 | GGATCACTAAGGCCA[C/G]GAGTTCGAGACCAGA | 267 |
rs185993030 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMFR | GRCh38.p7 | 16:56391197 | AAAATTAAATCCTAA[C/T]TCTTAAGCAACCACT | 267 |
rs186094725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56408196 | ATTCAAGGTCAATCT[C/T]GGCTTCTCTGCTTAG | 267 |
rs186111730 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | AMFR | GRCh38.p7 | 16:56370465 | ATGACTACAAAAGGA[C/T]CTAGTGGAGTTCTGG | 267 |
rs186184512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56423023 | TGGCAGGCAGTGTTC[A/G]TGAAAAAGTTGAATC | 267 |
rs186190676 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AMFR | GRCh38.p7 | 16:56376434 | ATGTCTGCTCTTAAA[A/G]CAGAAATCATTAACA | 267 |
rs186224843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56401517 | AACTAAGATGGCAAA[C/T]TATGGGTGGGAAACA | 267 |
rs186228488 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | AMFR | GRCh38.p7 | 16:56384444 | TTGTTCAATCAATCA[A/G]TAAAGATTAACTAAT | 267 |
rs186279738 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56424374 | CAGAAAAGGAAGCAC[A/G]GTTTGGTGTTTGTTT | 267 |
rs186315211 | snp | A/C/G | 0.00597247 | 0.0543191 | intron-variant | AMFR | GRCh38.p7 | 16:56378615 | TGGACTTCATTAAAT[A/C/G]TAAAAAGTTCTGCAA | 267 |
rs186384256 | snp | A/G | 0.00186619 | 0.0304896 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362201 | GGAGGGGACCCATGG[A/G]GCACACTCATGAGAT | 267 |
rs186489725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56414456 | GTGACTGAGCCTTTC[C/T]GGTTCTCTCCCAATG | 267 |
rs186528044 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56376899 | AATTACTAATACAAG[A/G]AATATTATACAGATA | 267 |
rs186552753 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AMFR | GRCh38.p7 | 16:56397220 | CTGCTATAAAGACAC[A/G]TGCACACGTTATGTT | 267 |
rs186608013 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | AMFR | GRCh38.p7 | 16:56409929 | CCCCAGCACTTTTGG[A/T]GGCTGAGGTGGGTAG | 267 |
rs186641052 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | AMFR | GRCh38.p7 | 16:56371781 | CTGATTCAGCCAGCC[C/T]TGGAGCAAGTGTTAC | 267 |
rs186817271 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56372370 | CCAGGTTCATTCATG[A/C]TGCAGCATGCAACAG | 267 |
rs186834569 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | AMFR | GRCh38.p7 | 16:56393626 | AAGGCCATTACATAA[C/T]GGTAAAGGGATCAAT | 267 |
rs186860393 | snp | C/G/T | 0.0023933 | 0.0345097 | intron-variant | AMFR | GRCh38.p7 | 16:56417068 | TTATTAATAACTATT[C/G/T]CATGTCTATTTATAG | 267 |
rs186921039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56373067 | TTGGTACAGACTCAG[C/T]GTAACAACTCTGAGA | 267 |
rs186931043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56410505 | CAATGTCAATGAATA[C/T]TCTCTGAATATACCA | 267 |
rs186931223 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | AMFR | GRCh38.p7 | 16:56394481 | GGGCGCAGTGGCTCA[C/T]GCCTGTAATCCCAGC | 267 |
rs186940112 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56399324 | ATATACCCAAAAGAA[C/G]TGAGAACAAGTCCTC | 267 |
rs186957867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56420864 | AGGACTACAGCACAG[A/G]CCACTACACTTAATT | 267 |
rs186990724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56413413 | CCAGCTACTTGGGAG[A/G]TTGAAGCAGGACAAG | 267 |
rs187010224 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56375716 | GATAAAGAACAGCAT[A/T]ACAAAATGATCATGG | 267 |
rs187133892 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56413805 | GATCATTCAAAATAA[A/G]ACAAATCTAGGCTTC | 267 |
rs187293389 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56396382 | GAAACAATACCACAC[A/C]TCTACAGCCATCTGA | 267 |
rs187343186 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56366524 | AAGAAGGCCTAGTAG[C/T]GTTTACTGTTTCCTC | 267 |
rs187380900 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | AMFR | GRCh38.p7 | 16:56398469 | ATATAGATATATATA[G/T]CCCTTGAAATGTAGA | 267 |
rs187389298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56418826 | AAAAAAAAGGAAATA[C/T]GTGCACACACGTTTG | 267 |
rs187394415 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56364644 | GGCTGGAGTGCAGTG[A/G]CACAATCTCTGCTCA | 267 |
rs187402844 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56380252 | CTGAAGCCCAATGGC[C/G]CCTTTCAGCCATGGC | 267 |
rs187472781 | snp | C/T | 1.65029e-05 | 0.00287248 | missense | AMFR | GRCh38.p7 | 16:56404995 | CATACGTCCCCTTTC[C/T]TTCCCACGTCCCTTC | 267 |
rs187528539 | snp | C/G | 0.000291163 | 0.0120622 | intron-variant | AMFR | GRCh38.p7 | 16:56385889 | CTCCTAATTCCCAGT[C/G]ATCTTCTTAAAGCAG | 267 |
rs187533318 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56368271 | CCCCACCCACAACCT[G/T]TGATTCCTGGGACCA | 267 |
rs187666294 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | AMFR | GRCh38.p7 | 16:56403341 | GAAACTCATCAGAAA[C/T]GGAAAAGCTTTATGC | 267 |
rs187702687 | snp | A/G | 8.2373e-05 | 0.00641714 | missense | AMFR | GRCh38.p7 | 16:56389296 | GTTCTTCCCTGACAC[A/G]ATTATTGTCGGCAAT | 267 |
rs187723758 | snp | C/G | 0.0154538 | 0.0865337 | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56425850 | CGGCCACTTGCCCCC[C/G]CCCCACCCCATTAAC | 267 |
rs187764153 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | AMFR | GRCh38.p7 | 16:56393952 | AAAATTGACCACATA[C/G]TTGGAAGTAAAGCAC | 267 |
rs187778425 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56364758 | ATCTGGCTAATTTTT[C/G]TATTTTTTGTAGAGA | 267 |
rs187801825 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56403746 | ATGGCTTAGAAGAAC[G/T]GATGTTAGCACAGGA | 267 |
rs187884665 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | AMFR | GRCh38.p7 | 16:56418018 | AAACACAACAAATGT[A/G]GCCAGGCATGGTGGT | 267 |
rs187924198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56379732 | CAAGTCCAAAATAAG[A/G]TAGGGCAGTCAAATC | 267 |
rs187974992 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56398074 | ATTTATAATATATAA[A/C]TGTATCATTTATAAT | 267 |
rs188024374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56381797 | TCCAATCCTATAGAG[A/G]GAACACAAATGTAAA | 267 |
rs188063832 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56410272 | CAGATTCTTACACAA[C/T]AGAAAAGATTAGACT | 267 |
rs188091154 | snp | A/C | 0.439224 | 0.163383 | intron-variant | AMFR | GRCh38.p7 | 16:56398096 | ATTTATAATATATAA[A/C]TGTATCATTTATAAT | 267 |
rs188111509 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56416684 | TGGGCTCAAGTGATC[C/T]GTCTGCCTCGGCCTC | 267 |
rs188127528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56378016 | TCAAGATGTCCATTC[C/T]TCCCAACTTGATGTA | 267 |
rs188449251 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56374323 | GAAACAATAATGGCT[A/G]AGAACTTGTCCAAAT | 267 |
rs188568070 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | AMFR | GRCh38.p7 | 16:56397720 | TCATTTATAATATAT[A/G]AATGTATCATTTATA | 267 |
rs188683089 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56388638 | ACCCTGTACAGCTGT[C/T]GAAAATATTTTCTTT | 267 |
rs188737648 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56395987 | AGGGATGTGAAGGAC[C/T]TCTCTTCAAGGAGAA | 267 |
rs188745443 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56413072 | GGGTTGAAAAGGGTA[C/G]GTAAGGAGAGAATGG | 267 |
rs188746885 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56383156 | ACTGTCCAACCCCTC[C/G]GGCAATGGAAAATGC | 267 |
rs188752568 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | AMFR | GRCh38.p7 | 16:56366241 | AAATTAGCCAGGCGT[A/G]GTGGTGGGCGCCTGT | 267 |
rs188765828 | snp | G/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56401264 | CAGACACAGCTCTTC[G/T]GTGCTGTTTAGCGGT | 267 |
rs188768093 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56375608 | AAGAAAATGGATTAA[C/G]AAAAATATACCACAC | 267 |
rs188819443 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMFR | GRCh38.p7 | 16:56415422 | AAAAGCAAATGATAA[C/T]TTTAAAGAAGAAAGA | 267 |
rs188854147 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56377483 | CTTTGTCACTGTGAT[A/G]AAGAATATCTACAAA | 267 |
rs188856214 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56416185 | ATTTAGCACTTGTTC[A/G]AGGCATGTGGGAAAT | 267 |
rs188916948 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56422421 | CCTCTCACAGCAGAG[A/C]CACCTGCCCCACCTC | 267 |
rs188995993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56369107 | AAATGATATTCAGCT[A/G]TTAAGTAACTAAAAC | 267 |
rs189060515 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56427107 | GAAAACAAAAGATCT[C/T]TCAAGCTTACAATTC | 267 |
rs189087689 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | AMFR | GRCh38.p7 | 16:56390565 | TGTTCCAAAATAATG[A/T]CATCTGTCTGTATGT | 267 |
rs189091645 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56369765 | TGGAATCAACCTAAG[C/T]GTCCTTCAACACAGG | 267 |
rs189099198 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56406773 | GAATAAACAGTAACA[A/T]GCTAAAATAAAAGTA | 267 |
rs189158139 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | AMFR | GRCh38.p7 | 16:56408324 | CATTTAATTTACTGA[C/G]TATAACAATATGCAT | 267 |
rs189277374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56391280 | TCTACAGCTCCCAGC[A/G]TGAGTGACGCAGAAG | 267 |
rs189308209 | snp | C/T | 0.00676609 | 0.0577691 | downstream-variant-500B | AMFR | GRCh38.p7 | 16:56361122 | AAACCTGTGAACATG[C/T]GGAATTAGTGGCACC | 267 |
rs189389097 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | AMFR | GRCh38.p7 | 16:56377856 | AGCGCAGTATGCTTT[A/G]TATTAGCGCCCACAA | 267 |
rs189582922 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56411398 | CATGACATCATGCCC[A/G]GCTAATGTTTTTTAT | 267 |
rs189667186 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56382202 | AGCCTTAAAAAGGAA[C/G]AAAATTCTGACTTGT | 267 |
rs189672362 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AMFR | GRCh38.p7 | 16:56370546 | TGTGTTGAACTGGAT[A/G]TTAAAAAGGGTAAAT | 267 |
rs189673261 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56422142 | TCTCACTCCACAAAA[C/T]ACTGTCCACACTTGG | 267 |
rs189678503 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56417636 | ATGCAGACTTACAAC[A/T]GTTTACTCAGTGTCC | 267 |
rs189802218 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | AMFR | GRCh38.p7 | 16:56410822 | GGGAGGTCGAGGTTG[C/T]AGGGAGCCATGATCA | 267 |
rs189816960 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56373693 | CACTAATGGATAAAG[A/T]GGACAGCATGCAGGA | 267 |
rs189819491 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | AMFR | GRCh38.p7 | 16:56376889 | AGAGGACCTAAATTA[C/G]TAATACAAGAAATAT | 267 |
rs189823308 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56423666 | TCCATATCACTTTGT[C/T]TACCTGCTAACTCAA | 267 |
rs189827960 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | AMFR | GRCh38.p7 | 16:56413809 | ATTCAAAATAAAACA[A/C]ATCTAGGCTTCTTTA | 267 |
rs189833917 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56396383 | AAACAATACCACACA[G/T]CTACAGCCATCTGAT | 267 |
rs189939369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56399776 | CTGAACTGTACACTT[C/T]AAAATAGTTAAATGT | 267 |
rs190084289 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AMFR | GRCh38.p7 | 16:56395353 | AGCTGGCTTCATTCC[C/T]GGGATGCAATGCTGG | 267 |
rs190113843 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56414817 | AAATAGGAGGTAGGG[G/T]TAGGAGTGTGGATGG | 267 |
rs190116506 | snp | A/G | 0.139225 | 0.224118 | intron-variant | AMFR | GRCh38.p7 | 16:56398125 | ATATATAAATGTATC[A/G]TTTATAATATATAAC | 267 |
rs190154623 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56361707 | AATTGTGGATAATAC[C/T]GGATTCTTCCCAAAA | 267 |
rs190294541 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | AMFR | GRCh38.p7 | 16:56367230 | CATGAGGGCAATCCC[A/C]AGGGAATGACTGCCA | 267 |
rs190374760 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56378657 | AAAAATAAGATGACA[A/G]GCCAGATTGGGAGAA | 267 |
rs190376664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56416763 | AGTCTTTGAATTCAA[A/G]TAAGGTATAAAAAAT | 267 |
rs190483804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56390818 | TTTATTTCACAGAGT[A/G]CAAAATCCTCCCACA | 267 |
rs190589342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56403497 | ACTATATAACTACAT[A/G]TTACTATTATATTTG | 267 |
rs190600808 | snp | A/C | | | intron-variant, upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56424531 | GAATTCTCCCCTCTG[A/C]CCTCTCCTCTTCGTC | 267 |
rs190627778 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | AMFR | GRCh38.p7 | 16:56387074 | CGCACTCCAGCCTGG[C/T]AACAGGGCAAGACTC | 267 |
rs190691260 | snp | A/T | 1.64974e-05 | 0.00287201 | intron-variant | AMFR | GRCh38.p7 | 16:56407957 | AGTCCTGCATCCAGT[A/T]TCTCACCTCTGCAGC | 267 |
rs190716490 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56370259 | AAACTTCTGATACAC[A/G]TAGCATGGATAAAAT | 267 |
rs190738895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56408972 | TAAAATGATTCACTT[C/T]GCAAACAAGGAAGCT | 267 |
rs190741299 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | AMFR | GRCh38.p7 | 16:56393259 | GCCACTGCAAAAACA[C/T]CCCAAATTGTAAAGA | 267 |
rs190760198 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | AMFR | GRCh38.p7 | 16:56379457 | CATTCCGCCCCGGCC[C/G]CTCCCAAATCTCATG | 267 |
rs190912369 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | AMFR | GRCh38.p7 | 16:56366821 | GTAGGGCAGAGGGCA[C/T]GGGCAGGGGGTGGGG | 267 |
rs190922000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56402064 | GTTGCTAGGCCGAGC[A/G]CGGTGGCTTATACCT | 267 |
rs190922921 | snp | C/T | 0 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56417081 | TTCCATGTCTATTTA[C/T]AGAAAAATACCTTAA | 267 |
rs190941204 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56379095 | GTTTAGCATTTGTAT[C/T]TGTCGTTTTCTCATT | 267 |
rs190965119 | snp | A/G | 0.139564 | 0.224285 | intron-variant | AMFR | GRCh38.p7 | 16:56398169 | ATATATAACTCTATC[A/G]TTTATATATATAACT | 267 |