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 |