SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3685 | snp | A/G | 0.377187 | 0.215229 | intron-variant | CHFR | GRCh38.p7 | 12:132864844 | CGCTGCCCTTTTTAA[A/G]TAGAACATTATCAAA | 55743 |
rs8021 | snp | A/G | 0.383632 | 0.211288 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132840699 | CACGGCCCCAAGCCC[A/G]GGGCTGGAGGCAGGT | 55743 |
rs15638 | snp | C/T | 0.380333 | 0.213338 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132840776 | CCAGGCTCGGGGCCG[C/T]GGTCACTCACACAAG | 55743 |
rs1045979 | snp | A/G | 0.253824 | 0.249971 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132841483 | AAAATACAGAGACAA[A/G]CACGTCAAGGTGTTT | 55743 |
rs1046106 | snp | C/T | 0 | 0 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132840474 | ACTTTTTTGCTTCTT[C/T]TCAGGAATACAGTTT | 55743 |
rs1046130 | snp | C/T | 0.0117874 | 0.0758601 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132840378 | TCTCTTTTGCATATT[C/T]TAATAAATGAGCCGC | 55743 |
rs2062161 | snp | A/G | 0.300926 | 0.244758 | intron-variant | CHFR | GRCh38.p7 | 12:132851446 | ATGTTACTAGATGGT[A/G]GGAAAAGATAGATTA | 55743 |
rs2062162 | snp | C/T | 0.336702 | 0.234484 | intron-variant | CHFR | GRCh38.p7 | 12:132856158 | ATGCCACACCCATGA[C/T]GAGTCGAAGCAAAGG | 55743 |
rs2062163 | snp | C/T | 0.0184896 | 0.0943553 | synonymous-codon | CHFR | GRCh38.p7 | 12:132856587 | TTGAGTGATTTTATT[C/T]CTGGCATCCATACTT | 55743 |
rs2076920 | snp | A/G | 0.487746 | 0.0773096 | downstream-variant-500B | CHFR | GRCh38.p7 | 12:132839877 | GAGCAGGGAGGTCCC[A/G]AGTTAGTGCAGGGGC | 55743 |
rs2128609 | snp | C/T | 0.0577344 | 0.159793 | intron-variant | CHFR | GRCh38.p7 | 12:132857018 | ATGCCCTCACGTGCC[C/T]GGGTGCTGGTGGAGG | 55743 |
rs2279313 | snp | C/T | 0.244776 | 0.249945 | intron-variant | CHFR | GRCh38.p7 | 12:132853048 | AGCTTCTGGTGACAT[C/T]GCCACTGCTGGGGAG | 55743 |
rs2291253 | snp | C/G | 0.493293 | 0.0575177 | intron-variant | CHFR | GRCh38.p7 | 12:132871967 | AGACCCCTGGTCCTA[C/G]GTTTTATTCCCCATA | 55743 |
rs2291254 | snp | A/G | 0.233235 | 0.249437 | intron-variant | CHFR | GRCh38.p7 | 12:132872229 | GAACGTTCAGAGAGC[A/G]CCCTCACGTGCACCC | 55743 |
rs2291255 | snp | A/C | 0.309401 | 0.24284 | intron-variant | CHFR | GRCh38.p7 | 12:132872781 | TTGCAGCCATCACAA[A/C]CCCGGTGAACTCATG | 55743 |
rs2306536 | snp | C/T | 0.303508 | 0.244207 | missense | CHFR | GRCh38.p7 | 12:132847076 | CCCGCTGGAGAGCCA[C/T]GAGGCTCTCGGTCAA | 55743 |
rs2306537 | snp | A/G | 0.354072 | 0.227318 | synonymous-codon | CHFR | GRCh38.p7 | 12:132847109 | TGTTTTTCCATGTCA[A/G]ACCTCTGGTTGCCAG | 55743 |
rs2306538 | snp | A/G | 0.320335 | 0.239902 | intron-variant | CHFR | GRCh38.p7 | 12:132847298 | CACGGCCTGCAGCAC[A/G]AGAAGTCTTGTCCAA | 55743 |
rs2306539 | snp | A/G | 0.273587 | 0.248885 | intron-variant | CHFR | GRCh38.p7 | 12:132856406 | CAGTAGTGAGCTCTC[A/G]GTCACGGTTGTGATG | 55743 |
rs2306540 | snp | C/T | 0.24449 | 0.249939 | intron-variant | CHFR | GRCh38.p7 | 12:132851545 | AGGTTACCCTAAGGC[C/T]AACACCGCTTTGAAA | 55743 |
rs2306541 | snp | A/G | 0.403429 | 0.197382 | missense | CHFR | GRCh38.p7 | 12:132851656 | TCCTGCTCGCGCTCC[A/G]CTCTCCGGTCGGGCA | 55743 |
rs2306542 | snp | C/G | 0.377187 | 0.215229 | intron-variant | CHFR | GRCh38.p7 | 12:132861688 | CAGCTCAGGAGAGAA[C/G]CATGCCTGTAAGGTG | 55743 |
rs2306543 | snp | C/T | 0.320335 | 0.239902 | intron-variant | CHFR | GRCh38.p7 | 12:132861691 | CTCAGGAGAGAACCA[C/T]GCCTGTAAGGTGTCA | 55743 |
rs2306544 | snp | C/T | 0.239614 | 0.249784 | intron-variant | CHFR | GRCh38.p7 | 12:132842832 | ATGCAGTTTTATCTC[C/T]GTCTTCCACTTCTGT | 55743 |
rs2306545 | snp | C/T | 0.301177 | 0.244706 | intron-variant | CHFR | GRCh38.p7 | 12:132842710 | GCAGTCACTGAGGGC[C/T]TCAGGCCCCCCTCGC | 55743 |
rs3741489 | snp | C/T | 0.301177 | 0.244706 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132841216 | CTAAAAACAGACTTC[C/T]GCTTTAACTGTAGTT | 55743 |
rs3741490 | snp | C/T | 0.380919 | 0.21298 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132841322 | CTGCTGATGCCACCA[C/T]GAGCCCTGCCCAGCG | 55743 |
rs3741492 | snp | C/T | 0.320575 | 0.239832 | intron-variant | CHFR | GRCh38.p7 | 12:132843688 | GAAAAGAGTGCTGGC[C/T]GAGCGTGGTGGCTCA | 55743 |
rs3741493 | snp | C/T | 0.0633504 | 0.166319 | intron-variant | CHFR | GRCh38.p7 | 12:132843809 | AAAAAATTAGCCGGG[C/T]GTGGTGGCGGGTGCC | 55743 |
rs3741494 | snp | C/T | 0.194278 | 0.243711 | upstream-variant-2KB, nc-transcript-variant | CHFR, LOC101928530 | GRCh38.p7 | 12:132887914 | GGAGTAGAAGACGGT[C/T]CATCTTAGTTGTCAC | 55743 |
rs3782223 | snp | A/G | 0.269267 | 0.249256 | intron-variant | CHFR | GRCh38.p7 | 12:132872863 | ACTAAATGCTGGGCC[A/G]TCAGCTGCAGGACAT | 55743 |
rs3782224 | snp | A/C | 0.249603 | 0.25 | intron-variant | CHFR | GRCh38.p7 | 12:132873251 | CCATAAACAGAGGGT[A/C]AACAGTGTAGGTTTT | 55743 |
rs3816759 | snp | C/T | 0.277507 | 0.248482 | intron-variant | CHFR | GRCh38.p7 | 12:132856651 | ATTGAAAGGACACAG[C/T]GCCATTCACCGGCAG | 55743 |
rs3832803 | in-del | -/A | 0.382085 | 0.212258 | downstream-variant-500B | CHFR | GRCh38.p7 | 12:132840327 | AAGTGAGGCAGCCCC[-/A]AGACACGAGCCCAAC | 55743 |
rs3832804 | in-del | -/AA | 0.478104 | 0.102316 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132841396 | TCTCACTCAGAGGGT[-/AA]AAAGCTCCACAGAAG | 55743 |
rs4237797 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | CHFR | GRCh38.p7 | 12:132865101 | AAATACTAGTAACCC[C/T]GCGTCCTGTCTGTGC | 55743 |
rs4303268 | snp | G/T | 0.0652144 | 0.168387 | intron-variant | CHFR | GRCh38.p7 | 12:132864792 | CACACCCGGCCAGAA[G/T]AATTTTTTTTTTAAT | 55743 |
rs4758887 | snp | G/T | 0.28578 | 0.247426 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886557 | AACCAGATGGTCACT[G/T]GGGAGACTGGAGGCA | 55743 |
rs4758888 | snp | A/G | 0.331179 | 0.236453 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886923 | CCATTACAGTCAGAA[A/G]AGATACTCTGTACGG | 55743 |
rs4758909 | snp | A/G | 0.0573587 | 0.15934 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132841203 | CTTGAAACTTTTCCT[A/G]AAAACAGACTTCTGC | 55743 |
rs4758910 | snp | A/G | 0.319856 | 0.240042 | intron-variant | CHFR | GRCh38.p7 | 12:132857630 | TCGACCAAGGTCCGC[A/G]GCAGCCCCACCACGG | 55743 |
rs4758911 | snp | A/C | 0.319856 | 0.240042 | intron-variant | CHFR | GRCh38.p7 | 12:132857917 | AATACACCTTCCCAG[A/C]TAAGGAGCATTTAAA | 55743 |
rs4758912 | snp | C/T | 0.039522 | 0.134904 | intron-variant | CHFR | GRCh38.p7 | 12:132865497 | CCTGTCTCAGCTTCC[C/T]GAGTAGCTGGGACTA | 55743 |
rs4758913 | snp | A/G | 0.0711525 | 0.174681 | intron-variant | CHFR | GRCh38.p7 | 12:132871665 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 55743 |
rs4758914 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | CHFR | GRCh38.p7 | 12:132878583 | GGTCCGGTGGCTCAC[A/G]ccgaggcgggcagat | 55743 |
rs4758948 | snp | A/G | 0.300421 | 0.244863 | intron-variant | CHFR | GRCh38.p7 | 12:132841810 | TAAAAATTTTGAAAC[A/G]GAAGTGCAAACATCT | 55743 |
rs4758949 | snp | C/T | 0.319616 | 0.240112 | intron-variant | CHFR | GRCh38.p7 | 12:132841970 | AAAAAATTAGCCTGA[C/T]GTGGTGGCGAGCACC | 55743 |
rs4758950 | snp | A/G | 0.319856 | 0.240042 | intron-variant | CHFR | GRCh38.p7 | 12:132843222 | ATAACTAGTTTCCTC[A/G]GACCGTTCTGAGATT | 55743 |
rs4758951 | snp | A/G | 0.473081 | 0.112848 | intron-variant | CHFR | GRCh38.p7 | 12:132845629 | CACTCCAGCCTGGGC[A/G]ACAGAGCAAGAACCT | 55743 |
rs4758952 | snp | A/G | 0.029116 | 0.117091 | intron-variant | CHFR | GRCh38.p7 | 12:132854398 | ACTCGACTGCTTCAC[A/G]TCTAAACATTGACGT | 55743 |
rs4758953 | snp | C/G | 0.301177 | 0.244706 | intron-variant | CHFR | GRCh38.p7 | 12:132854409 | TCACGTCTAAACATT[C/G]ACGTCACTGCGCATG | 55743 |
rs4758954 | snp | C/T | 0.320096 | 0.239972 | intron-variant | CHFR | GRCh38.p7 | 12:132857967 | TCTGTTTGCAGAGTT[C/T]ACGGGGTCACACACG | 55743 |
rs4758955 | snp | C/T | 0.326035 | 0.238157 | intron-variant | CHFR | GRCh38.p7 | 12:132859009 | CCCAGCCCTGCCCCA[C/T]ACGGGACGAAGAACC | 55743 |
rs5801995 | in-del | -/AGA | 0.245631 | 0.249962 | intron-variant | CHFR | GRCh38.p7 | 12:132864468 | CTTAGGCATACAGAT[-/AGA]AGAATTTTTATTTTT | 55743 |
rs6560907 | snp | C/T | 0.319856 | 0.240042 | intron-variant | CHFR | GRCh38.p7 | 12:132850359 | CAATGCCTCTATATA[C/T]GAAGCATGCTCTGTG | 55743 |
rs6560908 | snp | A/G | 0.37778 | 0.214877 | intron-variant | CHFR | GRCh38.p7 | 12:132852763 | CTACAAGAAGCCACT[A/G]AGAATGCAGCACAAG | 55743 |
rs6560909 | snp | A/G | 0.0733688 | 0.176922 | intron-variant | CHFR | GRCh38.p7 | 12:132878595 | CACAccgaggcgggc[A/G]gatcacaaggtcagg | 55743 |
rs6560910 | snp | A/G | 0.0741063 | 0.177655 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886141 | ATATGGCGAAAGCTC[A/G]TCTCTACTAAAAATA | 55743 |
rs7133593 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | CHFR | GRCh38.p7 | 12:132883407 | ctccagcctgagaaa[C/T]aggagtgaaactccg | 55743 |
rs7134338 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132851880 | CCCTGCTAAACCACC[A/G]GGGACCTTCTGCCAC | 55743 |
rs7136785 | snp | A/C | 0.248755 | 0.249997 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886500 | TGTTGACAGGACCAG[A/C]GCATTTCTCTCCCCA | 55743 |
rs7297261 | snp | A/T | 0.377187 | 0.215229 | intron-variant | CHFR | GRCh38.p7 | 12:132856067 | GACTTTATAGTCGCT[A/T]GATCAACTACAAAGA | 55743 |
rs7297272 | snp | A/C | 0.370568 | 0.219005 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886173 | AAAAATTAGCCAGGC[A/C]TGGTGGCGCACGCCT | 55743 |
rs7300520 | snp | G/T | 0.332799 | 0.23589 | intron-variant | CHFR | GRCh38.p7 | 12:132866932 | CCAGCTACTCAGGAG[G/T]CTGAGGCAGGGGAAT | 55743 |
rs7300955 | snp | C/T | 0.370365 | 0.219117 | intron-variant | CHFR | GRCh38.p7 | 12:132881792 | agaatggcttgaacc[C/T]gggaggcggaggttg | 55743 |
rs7301483 | snp | C/G/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132868987 | ggggaaggggacatg[C/G/T]ggagtgactgctgct | 55743 |
rs7301492 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132869001 | gcggagtgactgctg[C/G]tgggGCTGAGGGGAA | 55743 |
rs7301501 | snp | C/G/T | 0 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132869026 | ggggaaggggacatg[C/G/T]ggagtgactgctgct | 55743 |
rs7301505 | snp | C/G | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132869040 | gcggagtgactgctg[C/G]tggggtcgaggGGAA | 55743 |
rs7301970 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132846444 | attttttgtattttt[C/T]tttttttagtagaga | 55743 |
rs7304156 | snp | G/T | 0.379354 | 0.213933 | intron-variant | CHFR | GRCh38.p7 | 12:132867289 | CCTGCACCCGATGCC[G/T]CTCCTTCCCCAAATC | 55743 |
rs7308940 | snp | A/C | 0.0704125 | 0.17392 | intron-variant | CHFR | GRCh38.p7 | 12:132864101 | ATAACCTATATCTTA[A/C]TAAAGACTTAGTTTA | 55743 |
rs7311425 | snp | C/T | 0 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132869046 | tgactgctgctgggg[C/T]cgaggGGAAGGGGAC | 55743 |
rs7312722 | snp | C/T | 0.377385 | 0.215112 | intron-variant | CHFR | GRCh38.p7 | 12:132864094 | GGTGTGAATAACCTA[C/T]ATCTTAATAAAGACT | 55743 |
rs7314999 | snp | A/G | 0.319856 | 0.240042 | intron-variant | CHFR | GRCh38.p7 | 12:132850563 | ACCGCCCAGATCACC[A/G]GGTGTGTCCCACGGC | 55743 |
rs7954583 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132873089 | AGAGCACAGCATACC[C/T]GACACACAAAACGGC | 55743 |
rs7954854 | snp | C/T | 0.370162 | 0.219229 | intron-variant | CHFR | GRCh38.p7 | 12:132883626 | cagctacttgggagg[C/T]tgaggcaggagaatg | 55743 |
rs7957697 | snp | C/G | 0.245916 | 0.249967 | intron-variant | CHFR | GRCh38.p7 | 12:132879297 | accgcacctggccTG[C/G]GATAGGCATTTGTAC | 55743 |
rs7958545 | snp | A/T | 0.116838 | 0.211584 | intron-variant | CHFR | GRCh38.p7 | 12:132854202 | CACAGTGAAAAGACA[A/T]TTTTTTCATAAGGAA | 55743 |
rs7961664 | snp | C/T | 0 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132880270 | aagacaggcaaaaat[C/T]ttagtgccgttgggt | 55743 |
rs7961946 | snp | C/T | 0.386694 | 0.20932 | intron-variant | CHFR | GRCh38.p7 | 12:132880526 | agctgggcgtgatgg[C/T]gggcgcctgtagtcc | 55743 |
rs7962983 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132879066 | ctggagtgcagtggc[A/G]ccatctcggctcacc | 55743 |
rs7963065 | snp | A/C | 0.390651 | 0.206682 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886347 | AAAAAAACCAGGTGC[A/C]AGCACATTATAAGGG | 55743 |
rs7963336 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | CHFR | GRCh38.p7 | 12:132875670 | TGAGTAACACTGACA[C/T]AGACttcccttccga | 55743 |
rs7963509 | snp | A/G | 0.0737376 | 0.17729 | intron-variant | CHFR | GRCh38.p7 | 12:132879460 | cagtggcacgatctc[A/G]gctcactgcaacctc | 55743 |
rs7966176 | snp | A/G | 0.319856 | 0.240042 | intron-variant | CHFR | GRCh38.p7 | 12:132853951 | AAAGCAGAGCGCGGT[A/G]GGCAACGTACTGGGA | 55743 |
rs7966344 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CHFR | GRCh38.p7 | 12:132878978 | CTGAGCCAACTGTGA[C/T]AGGCATTTGTTTTTt | 55743 |
rs7966694 | snp | G/T | 0.0630642 | 0.166377 | intron-variant | CHFR | GRCh38.p7 | 12:132879275 | gttgggattacaggc[G/T]tgagccaccgcacct | 55743 |
rs7969859 | snp | A/G | 0.376791 | 0.215463 | intron-variant | CHFR | GRCh38.p7 | 12:132860654 | ATAATCTTAACTTTG[A/G]CTTTCAAAGTGCAGA | 55743 |
rs7975454 | snp | C/T | 0.00447708 | 0.0471009 | synonymous-codon | CHFR | GRCh38.p7 | 12:132848720 | AGGCTGCAGGCAGAC[C/T]GCACCTGTGGAGAGA | 55743 |
rs7977432 | snp | C/T | 0.478932 | 0.10045 | intron-variant | CHFR | GRCh38.p7 | 12:132854010 | ATCACTTGTCTTTTC[C/T]ACACTTCCCTTGTAC | 55743 |
rs9630294 | snp | C/T | 0.23846 | 0.249734 | intron-variant | CHFR | GRCh38.p7 | 12:132879459 | GCAGTGGCACGATCT[C/T]AGCTCACTGCAACCT | 55743 |
rs9634239 | snp | C/T | 0.340784 | 0.232934 | intron-variant | CHFR | GRCh38.p7 | 12:132849526 | GCTCCACCACCCTAA[C/T]ACGGCTTCGATGGGC | 55743 |
rs9738468 | snp | C/T | 0.319856 | 0.240042 | intron-variant | CHFR | GRCh38.p7 | 12:132863594 | GAGGGATGCATAGCT[C/T]CCAACGGGTGGAGAT | 55743 |
rs9943702 | snp | A/G | 0.319616 | 0.240112 | intron-variant | CHFR | GRCh38.p7 | 12:132864830 | gtaatatataaataC[A/G]CTGCCCTTTTTAAGT | 55743 |
rs9943754 | snp | A/C | 0.319856 | 0.240042 | intron-variant | CHFR | GRCh38.p7 | 12:132864733 | ACCTCAGGCGATCCA[A/C]CCACCCGGCCTCCCA | 55743 |
rs9943856 | snp | A/G | 0.376197 | 0.215811 | intron-variant, missense | CHFR | GRCh38.p7 | 12:132862416 | tgggcaacacagcaa[A/G]gcaccatctctacaa | 55743 |
rs9943858 | snp | A/G | 0.0704125 | 0.17392 | intron-variant | CHFR | GRCh38.p7 | 12:132862529 | ggatcacttgagccc[A/G]ggagttcgaggctac | 55743 |
rs10573381 | in-del | -/TT | 0.352504 | 0.228019 | intron-variant | CHFR | GRCh38.p7 | 12:132846264 | TCTTTTTTTTTTTTT[-/TT]TTGAGACGGAGTCTC | 55743 |
rs10616057 | in-del | -/AA | 0 | 0 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886389 | CAAAAAAAAAAAAAA[-/AA]TTGCTTCCAAACAGC | 55743 |
rs10713171 | in-del | -/A | | | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886375 | GGGGTGAAATTAACC[-/A]AAAAAAAAAAAAAAA | 55743 |
rs10747087 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | CHFR | GRCh38.p7 | 12:132847280 | TGCAGAGGGCTGCAC[A/G]TTCACGGCCTGCAGC | 55743 |
rs10747088 | snp | A/T | 0.357238 | 0.225832 | intron-variant | CHFR | GRCh38.p7 | 12:132867959 | AATAGCTAAGAAAAT[A/T]AAAAAAAAATAATAT | 55743 |
rs10781657 | snp | A/T | 0.220544 | 0.248259 | intron-variant | CHFR | GRCh38.p7 | 12:132845469 | TCTCAAAAAAAAAAA[A/T]AAATAAATAAATAAA | 55743 |
rs10781658 | snp | A/T | 0.077417 | 0.180873 | intron-variant | CHFR | GRCh38.p7 | 12:132845477 | AAAAAAATAAATAAA[A/T]AAATAAAAATAAAAA | 55743 |
rs10781659 | snp | A/C | 0.245631 | 0.249962 | intron-variant | CHFR | GRCh38.p7 | 12:132854770 | AAGATCCAGCCACTG[A/C]ACTCCAGCCTGGGCA | 55743 |
rs10781660 | snp | A/C | 0.34101 | 0.232846 | intron-variant | CHFR | GRCh38.p7 | 12:132855233 | GGCAACAGAGCGAGA[A/C]TTTGTCTCGAAAAAA | 55743 |
rs10781661 | snp | A/G | 0.34101 | 0.232846 | intron-variant | CHFR | GRCh38.p7 | 12:132855393 | TGCCATTGGCAGGGC[A/G]CAGTGGCTCATGCCT | 55743 |
rs10781662 | snp | C/T | 0.479421 | 0.0993283 | intron-variant | CHFR | GRCh38.p7 | 12:132858220 | AAAAAATTAGCCAGA[C/T]GTGGTGACGCATGCC | 55743 |
rs10781663 | snp | A/G | 0.478768 | 0.100824 | intron-variant | CHFR | GRCh38.p7 | 12:132868266 | GGAGGCCGATCGGAC[A/G]GATCACGAGGTCAGG | 55743 |
rs10870525 | snp | C/T | 0.319616 | 0.240112 | intron-variant | CHFR | GRCh38.p7 | 12:132854982 | CGCGGTGGCTCACAC[C/T]TATAATCCCAGCACT | 55743 |
rs10870526 | snp | A/C | 0.237014 | 0.249662 | intron-variant | CHFR | GRCh38.p7 | 12:132867442 | CAACAGATCCATGGA[A/C]AGCAAAGGTCCCTTC | 55743 |
rs10870527 | snp | A/T | 0.245631 | 0.249962 | intron-variant | CHFR | GRCh38.p7 | 12:132867824 | AAGAGCTTAACAAAC[A/T]AGGAGAAACACCATT | 55743 |
rs10870528 | snp | C/T | 0.340333 | 0.233109 | intron-variant | CHFR | GRCh38.p7 | 12:132868270 | GCCGATCGGACAGAT[C/T]ACGAGGTCAGGAGAT | 55743 |
rs10870529 | snp | C/T | 0.379158 | 0.214052 | intron-variant | CHFR | GRCh38.p7 | 12:132868464 | CCGAGATCGCGCCAC[C/T]GCACTCCAGCCTGGG | 55743 |
rs10870530 | snp | C/T | 0.380919 | 0.21298 | intron-variant | CHFR | GRCh38.p7 | 12:132871269 | CCAGCCTGGCCAACA[C/T]GGCGAAACCCTGTCT | 55743 |
rs10870531 | snp | C/G | 0.479177 | 0.0998894 | intron-variant | CHFR | GRCh38.p7 | 12:132871428 | TTGCACTCCAGCCTC[C/G]GCAACAGAGCAGAGC | 55743 |
rs10870532 | snp | C/T | 0.235564 | 0.249583 | intron-variant | CHFR | GRCh38.p7 | 12:132874048 | TGCCAAGGAACGTGG[C/T]ACCTCTGGAACCTGG | 55743 |
rs10870533 | snp | A/G | 0.285519 | 0.247464 | intron-variant | CHFR | GRCh38.p7 | 12:132881035 | ACTTTGGGTGGCCAA[A/G]GCGGGCGGATCACTT | 55743 |
rs11147106 | snp | C/T | 0.319856 | 0.240042 | intron-variant | CHFR | GRCh38.p7 | 12:132844323 | GGAGTCTCGCTCTGT[C/T]GCCCTGGCTGGAGTG | 55743 |
rs11147107 | snp | A/G | 0.386313 | 0.209568 | intron-variant | CHFR | GRCh38.p7 | 12:132844923 | CAGGCGTGAGCCTCC[A/G]CGCCCGGCCCCACAT | 55743 |
rs11147108 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | CHFR | GRCh38.p7 | 12:132850525 | GTGGCCAGCGCCTGC[C/T]GTGGATGACCCCCGA | 55743 |
rs11147109 | snp | C/G | 0.237303 | 0.249677 | intron-variant | CHFR | GRCh38.p7 | 12:132853831 | TCCCCAGGGTCACTA[C/G]GTCCCCACTGACGTG | 55743 |
rs11147110 | snp | C/T | 0.306804 | 0.243461 | intron-variant | CHFR | GRCh38.p7 | 12:132856654 | GAAAGGACACAGCGC[C/T]ATTCACCGGCAGTGA | 55743 |
rs11147111 | snp | C/T | 0.307296 | 0.243346 | intron-variant | CHFR | GRCh38.p7 | 12:132856714 | CTGGGAGCTCGCGTG[C/T]GCAGTGCTGCGGAAG | 55743 |
rs11147112 | snp | A/G | 0.0101123 | 0.0703837 | intron-variant | CHFR | GRCh38.p7 | 12:132859052 | TTCCGTGAGCCAAGG[A/G]TGAACACGGTCGCAC | 55743 |
rs11147113 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CHFR | GRCh38.p7 | 12:132861393 | AATGCCCCACAGCAC[A/G]GAGCATGGCAGCGGC | 55743 |
rs11147114 | snp | C/T | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132865653 | GCTGGGATTACAGGT[C/T]TTTTTTTTTTTTTTT | 55743 |
rs11147115 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CHFR | GRCh38.p7 | 12:132867730 | TATGGAATGTAAGAA[C/T]GCGAGAGCCAAGCAC | 55743 |
rs11147116 | snp | A/G | 0.319616 | 0.240112 | intron-variant | CHFR | GRCh38.p7 | 12:132867733 | GGAATGTAAGAACGC[A/G]AGAGCCAAGCACTCC | 55743 |
rs11147117 | snp | A/T | 0.283158 | 0.247791 | intron-variant | CHFR | GRCh38.p7 | 12:132867969 | AAAATTAAAAAAAAA[A/T]AATATGTATAGCGCG | 55743 |
rs11147118 | snp | C/T | 0.319616 | 0.240112 | intron-variant | CHFR | GRCh38.p7 | 12:132868021 | TGTACACATCCTCCA[C/T]GTGACAAACCCTAAA | 55743 |
rs11147119 | snp | C/T | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132868536 | CAAAAAAAAATTAGC[C/T]GGGCGTGGTTGCAGG | 55743 |
rs11147120 | snp | A/G | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132868573 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 55743 |
rs11147121 | snp | A/G | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132868656 | CTGCACTCCAGCCTG[A/G]GCGACAGAGCGAGAC | 55743 |
rs11147122 | snp | A/G | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132868675 | ACAGAGCGAGACTCC[A/G]TCTCAACAACAACAA | 55743 |
rs11147123 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132869118 | GGGGAGTGACTGCTG[A/G]TGGGGCCGAGGGGAA | 55743 |
rs11147124 | snp | C/T | 0.340559 | 0.233022 | intron-variant | CHFR | GRCh38.p7 | 12:132870236 | gactgcctgtagtcc[C/T]agctactcgggaggc | 55743 |
rs11147125 | snp | A/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132870552 | AAAAAAAAAAAAAAA[A/T]GGGAGACTGAAGCAG | 55743 |
rs11147126 | snp | C/T | 0.319376 | 0.240181 | intron-variant | CHFR | GRCh38.p7 | 12:132870638 | GCACTCCAGCCTGGG[C/T]AACAGAGCGAGACTC | 55743 |
rs11147127 | snp | C/T | 0.234982 | 0.249549 | intron-variant | CHFR | GRCh38.p7 | 12:132873744 | TACGGGGCTAGAGTG[C/T]GCACGGACTTGGGTG | 55743 |
rs11147128 | snp | A/G | 0.234982 | 0.249549 | intron-variant | CHFR | GRCh38.p7 | 12:132873745 | ACGGGGCTAGAGTGT[A/G]CACGGACTTGGGTGC | 55743 |
rs11147129 | snp | C/T | 0 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132874637 | GACCAGCACCCAGCG[C/T]GGGGAAGCCAGGCCC | 55743 |
rs11147130 | snp | A/G | 0.444444 | 0.157135 | intron-variant | CHFR | GRCh38.p7 | 12:132874641 | AGCACCCAGCGCGGG[A/G]AAGCCAGGCCCCGGA | 55743 |
rs11147131 | snp | A/G | 0.444444 | 0.157135 | intron-variant | CHFR | GRCh38.p7 | 12:132874654 | GGGAAGCCAGGCCCC[A/G]GAACAGGCGGGACTG | 55743 |
rs11147132 | snp | A/G | 0.250168 | 0.25 | intron-variant | CHFR | GRCh38.p7 | 12:132874954 | GGACCAGCACCCAGC[A/G]CGGGGAAGCCAGGCC | 55743 |
rs11147133 | snp | C/T | 0.24932 | 0.249999 | intron-variant | CHFR | GRCh38.p7 | 12:132874955 | GACCAGCACCCAGCA[C/T]GGGGAAGCCAGGCCC | 55743 |
rs11147134 | snp | G/T | 0.238749 | 0.249747 | intron-variant | CHFR | GRCh38.p7 | 12:132875382 | TGTGGGGGCTCACAC[G/T]TGCAATCCCAGCACT | 55743 |
rs11147135 | snp | A/G | 0.272511 | 0.248984 | intron-variant | CHFR | GRCh38.p7 | 12:132875489 | TGAGCTAGGCGTGGC[A/G]GCGGGCACCTGTAAT | 55743 |
rs11147136 | snp | A/G | 0.240765 | 0.249829 | intron-variant | CHFR | GRCh38.p7 | 12:132876952 | GGCGCATGCCACAAC[A/G]CCCGGCTAATTTTTA | 55743 |
rs11147137 | snp | C/T | 0.235564 | 0.249583 | intron-variant | CHFR | GRCh38.p7 | 12:132877708 | TGGTAACTGTGAACA[C/T]TACTGCACTTTGTTT | 55743 |
rs11147138 | snp | A/G | 0.27278 | 0.24896 | intron-variant | CHFR | GRCh38.p7 | 12:132880783 | CAGCCTGACCAACAT[A/G]GTGAAACCCAGTCTC | 55743 |
rs11147139 | snp | A/G | 0.25634 | 0.24992 | intron-variant | CHFR | GRCh38.p7 | 12:132881065 | TCAGACCAGGACTTC[A/G]AGACCAGCCTGGCCA | 55743 |
rs11147140 | snp | C/G | 0.235273 | 0.249566 | intron-variant | CHFR | GRCh38.p7 | 12:132881568 | ccaaataagaattgg[C/G]tgaaaatactgacca | 55743 |
rs11147141 | snp | C/T | 0.240765 | 0.249829 | intron-variant | CHFR | GRCh38.p7 | 12:132882653 | AACCAGTGCAAGTCA[C/T]GGTGTCGCCAGAGCC | 55743 |
rs11147142 | snp | C/T | 0.271702 | 0.249056 | intron-variant | CHFR | GRCh38.p7 | 12:132882684 | AGTTTGTAACAGAGG[C/T]GTCTCCATGCCAGAA | 55743 |
rs11147143 | snp | G/T | 0.272241 | 0.249009 | intron-variant | CHFR | GRCh38.p7 | 12:132882759 | TACCCCAGCTGTGGT[G/T]CAGTGGAGCAATCAC | 55743 |
rs11147144 | snp | A/C | 0.370568 | 0.219005 | intron-variant | CHFR | GRCh38.p7 | 12:132885743 | ATTAACTCCTCAGAG[A/C]AAATCTATGAAGTAG | 55743 |
rs11147145 | snp | A/T | 0.421842 | 0.181577 | upstream-variant-2KB, nc-transcript-variant | CHFR, LOC101928530 | GRCh38.p7 | 12:132888526 | TATATAGGTATAGGC[A/T]TAGTTATCTATACCT | 55743 |
rs11147146 | snp | C/G | 0.421684 | 0.181726 | upstream-variant-2KB, downstream-variant-500B | CHFR, LOC101928530 | GRCh38.p7 | 12:132888572 | AAATTGTAAGCCTCC[C/G]CAACCAACTGAATGA | 55743 |
rs11287044 | in-del | -/T | 0.491834 | 0.0633738 | intron-variant | CHFR | GRCh38.p7 | 12:132882707 | TGCCAGAACATCAGG[-/T]TTTTTTTTTTTTCTT | 55743 |
rs11376353 | in-del | -/A | | | intron-variant | CHFR | GRCh38.p7 | 12:132864177 | AGTGTTATTATTTGA[-/A]AAAAAAAAAACACAA | 55743 |
rs11432532 | in-del | -/G | 0.0711525 | 0.174681 | intron-variant | CHFR | GRCh38.p7 | 12:132852458 | ATCGATGTGGCAGCA[-/G]GAAGTCTGAGCCCAC | 55743 |
rs11542904 | snp | C/T | | | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132840428 | CAGATTGCTGCTTCT[C/T]AGTTTCTATCAAGAG | 55743 |
rs11608499 | snp | C/T | 0.245346 | 0.249957 | intron-variant | CHFR | GRCh38.p7 | 12:132883387 | gccgagatcacatca[C/T]tgcactccagcctga | 55743 |
rs11609361 | snp | C/G | 0.177503 | 0.239258 | intron-variant | CHFR | GRCh38.p7 | 12:132862680 | cgcctcctgggttga[C/G]gccattctcctgcct | 55743 |
rs11610826 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132858388 | caaaaacaaaaaacc[A/C]ccccgggctacatgg | 55743 |
rs11610829 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132858426 | gtctctacaaaaaac[A/C]caaaaatcagcaggg | 55743 |
rs11610954 | snp | C/T | 0.110167 | 0.207236 | intron-variant | CHFR | GRCh38.p7 | 12:132865194 | GGGGCTGTCCCTGCA[C/T]GGGGAGAGTCAGTGC | 55743 |
rs11611368 | snp | A/G | 0.323671 | 0.238899 | intron-variant | CHFR | GRCh38.p7 | 12:132849363 | TGATGCACTGCACCC[A/G]GCCTCAGACCCGTAT | 55743 |
rs11612050 | snp | G/T | 0.272511 | 0.248984 | intron-variant | CHFR | GRCh38.p7 | 12:132875081 | AAGCCAGGCCCTGAA[G/T]CAGGCGGGACAGCTA | 55743 |
rs11613325 | snp | A/G | 0.130008 | 0.219321 | intron-variant | CHFR | GRCh38.p7 | 12:132843252 | TTCAGGAAAGGAAAC[A/G]CATGTTTAACTAAAA | 55743 |
rs11614340 | snp | C/T | 0.245346 | 0.249957 | intron-variant | CHFR | GRCh38.p7 | 12:132849897 | CCAGCCTAGGTGGCC[C/T]TTTTCTACCTAGGTA | 55743 |
rs11615786 | snp | C/G | 0.319856 | 0.240042 | intron-variant | CHFR | GRCh38.p7 | 12:132862833 | gatccacctgcctca[C/G]cctcccaaagtgctg | 55743 |
rs11615963 | snp | C/T | 0.319856 | 0.240042 | intron-variant | CHFR | GRCh38.p7 | 12:132852692 | GCAAACCCAGGCTGG[C/T]GGATGGGCATCCATA | 55743 |
rs11836283 | snp | A/T | 0.325091 | 0.238456 | intron-variant | CHFR | GRCh38.p7 | 12:132845465 | TCCATCTCAAAAAAA[A/T]AAATAAATAAATAAA | 55743 |
rs12297152 | snp | C/T | 0.240765 | 0.249829 | intron-variant | CHFR | GRCh38.p7 | 12:132883830 | AAAATAATCAAGTTC[C/T]GTctgggcgaggtgg | 55743 |
rs12298063 | snp | C/T | | | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132885981 | TAAAATAAACTTTGA[C/T]TTGATACTGGAATGT | 55743 |
rs12298065 | snp | C/T | | | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132885988 | AACTTTGACTTGATA[C/T]TGGAATGTAAGACTA | 55743 |
rs12304978 | snp | A/G | 0.0707826 | 0.174302 | intron-variant | CHFR | GRCh38.p7 | 12:132858863 | GTCAGAGAACCGCTC[A/G]ATCCTGGGAGGGAGA | 55743 |
rs12305153 | snp | C/G | 0.286303 | 0.24735 | intron-variant | CHFR | GRCh38.p7 | 12:132873443 | GGAAGATGCGGTTTT[C/G]AGCTGTGCAGATGCA | 55743 |
rs12305506 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132865814 | acaggcatgcaccac[C/T]acacccggctaattt | 55743 |
rs12306797 | snp | C/T | 0.240478 | 0.249819 | intron-variant | CHFR | GRCh38.p7 | 12:132871628 | AATACAAAAATGAGC[C/T]GGGCGTGGTGGTGGG | 55743 |
rs12306980 | snp | C/G | 0 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132844149 | TCTGGAAGAAACACA[C/G]CCAGTTACCCAGCAA | 55743 |
rs12307101 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132874538 | ACCCAGCGCGGGGAA[A/G]CCAGGCCCCGGAACA | 55743 |
rs12314382 | snp | A/G | 0.24449 | 0.249939 | intron-variant | CHFR | GRCh38.p7 | 12:132849124 | GCTAATTTATTTTTT[A/G]TTTTTGTAGAGACAG | 55743 |
rs12314895 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132878833 | tcaaaaaaaaaaaaa[A/G]aaaaaaaaaaaCTCA | 55743 |
rs12315353 | snp | A/G | | | synonymous-codon | CHFR | GRCh38.p7 | 12:132859097 | CAGCAGGTCCTGGCA[A/G]ATGATGCATGTCAGC | 55743 |
rs12316858 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132874584 | GACCAGCACCCAGCG[C/T]GGGAAAGCCAGGCCC | 55743 |
rs12319441 | snp | C/T | 0.239614 | 0.249784 | intron-variant | CHFR | GRCh38.p7 | 12:132883446 | aaaaaaaaaaaaaGA[C/T]Tgggcgcagtggctc | 55743 |
rs12319552 | snp | C/G | 0.240765 | 0.249829 | intron-variant | CHFR | GRCh38.p7 | 12:132883649 | ggagaatggtgtgaa[C/G]ccaagaggcagagct | 55743 |
rs12321728 | snp | A/G | 0.245346 | 0.249957 | intron-variant | CHFR | GRCh38.p7 | 12:132857279 | CACCCTCACGTGCCC[A/G]GGTGCTGGTGGAGGG | 55743 |
rs12322443 | snp | A/C | 0.239614 | 0.249784 | intron-variant | CHFR | GRCh38.p7 | 12:132883917 | gaggccaggagttca[A/C]gaccagcctgaccaa | 55743 |
rs12368004 | snp | A/C | 0.478932 | 0.10045 | intron-variant | CHFR | GRCh38.p7 | 12:132864188 | TTTGAAAAAAAAAAA[A/C]ACAAGAAACTGGCTT | 55743 |
rs12369022 | snp | A/G | 0.319856 | 0.240042 | intron-variant | CHFR | GRCh38.p7 | 12:132844929 | tgagcctccacgccc[A/G]gccCCACATGGatat | 55743 |
rs12371351 | snp | A/G | 0.319856 | 0.240042 | intron-variant | CHFR | GRCh38.p7 | 12:132845050 | GGAAAGGATTTGTAC[A/G]TTTGGCTATCTACAA | 55743 |
rs12371596 | snp | C/T | 0.279713 | 0.250853 | intron-variant | CHFR | GRCh38.p7 | 12:132876955 | GCATGCCACAACGCC[C/T]GGCTAATTTTTATAT | 55743 |
rs12422323 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132855769 | AGCAAAATCTTAATG[C/T]TAAAGTGGTTTTGGT | 55743 |
rs12422391 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132858670 | gaggctgaggttgta[C/G]tgagccaagactgtg | 55743 |
rs12425387 | snp | C/T | 0.375 | 0.216506 | intron-variant | CHFR | GRCh38.p7 | 12:132874556 | AGGCCCCGGAACAGG[C/T]GGGACTGCCCAGGAC | 55743 |
rs12425404 | snp | C/T | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132874706 | GAGGAAGCCAGGCCC[C/T]GGAACAGGCAGGAAG | 55743 |
rs12425426 | snp | C/T | 0.239902 | 0.249796 | intron-variant | CHFR | GRCh38.p7 | 12:132844791 | GTGTGCCACCGTGCC[C/T]GGCTAATGTTTATAC | 55743 |
rs12425937 | snp | A/G | 0.375 | 0.216506 | intron-variant | CHFR | GRCh38.p7 | 12:132874620 | CAGGCGGGACTGCCC[A/G]GGACCAGCACCCAGC | 55743 |
rs12426236 | snp | G/T | 0.375 | 0.216506 | intron-variant | CHFR | GRCh38.p7 | 12:132874562 | CGGAACAGGCGGGAC[G/T]GCCCAGGACCAGCAC | 55743 |
rs12578891 | snp | A/C | 0.245061 | 0.249951 | intron-variant | CHFR | GRCh38.p7 | 12:132861395 | TGCCCCACAGCACGG[A/C]GCATGGCAGCGGCCC | 55743 |
rs12579117 | snp | A/G | 0.239614 | 0.249784 | intron-variant | CHFR | GRCh38.p7 | 12:132841878 | TTGGGAGGCCGAGGC[A/G]GGCGGATCACTTGAG | 55743 |
rs12579395 | snp | G/T | 0.239902 | 0.249796 | intron-variant | CHFR | GRCh38.p7 | 12:132842132 | AAAAAAAAAAAAGAA[G/T]TGCAAACATCTTAGA | 55743 |
rs12809384 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | CHFR | GRCh38.p7 | 12:132869266 | ggggacatgtggagt[C/G]actgctggtgggcac | 55743 |
rs12810281 | snp | A/T | 0.490563 | 0.0680388 | upstream-variant-2KB | CHFR | GRCh38.p7 | 12:132889100 | tcgcttgagcccagg[A/T]attcagaccatcctg | 55743 |
rs12811327 | snp | A/G | 0.358303 | 0.225323 | intron-variant | CHFR | GRCh38.p7 | 12:132872591 | CGCCCACTTCTCCCT[A/G]ACTGACAGCCTAACC | 55743 |
rs12811898 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132874847 | AGGACCAGCACCCAG[C/T]GCAGGGAACCCAGGC | 55743 |
rs12811926 | snp | A/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132874880 | TGGAACAGGCGGGAC[A/T]GCCCAGGACCAGCAC | 55743 |
rs12812091 | snp | A/T | 0.387263 | 0.208947 | intron-variant | CHFR | GRCh38.p7 | 12:132845464 | TTCCATCTCAAAAAA[A/T]AAAATAAATAAATAA | 55743 |
rs12812769 | snp | A/G | 0.377187 | 0.215229 | intron-variant | CHFR | GRCh38.p7 | 12:132858859 | TGAGGTCAGAGAACC[A/G]CTCAATCCTGGGAGG | 55743 |
rs12812907 | snp | A/G | 0.391769 | 0.205917 | intron-variant | CHFR | GRCh38.p7 | 12:132881800 | ttgaacccgggaggc[A/G]gaggttgcagtgagc | 55743 |
rs12814571 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132868346 | ATACAAAAAATTAGC[C/T]AGGCGTGGTGACGGG | 55743 |
rs12815689 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | CHFR | GRCh38.p7 | 12:132839862 | TCCCCTCTCAGCCTC[A/G]CCCCTGCACTAACTT | 55743 |
rs12816653 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132879073 | gcagtggcaccatct[C/G]ggctcaccacaacct | 55743 |
rs12816668 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132877895 | gcaagctccgcctcc[C/T]aggttcacaccattc | 55743 |
rs12816679 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132877903 | cgcctcccaggttca[C/T]accattctcctgcct | 55743 |
rs12817928 | snp | A/G | 0.382666 | 0.211895 | intron-variant | CHFR | GRCh38.p7 | 12:132873558 | GCTGGCTACGGGGCT[A/G]GAGTGCACACGGACT | 55743 |
rs12819660 | snp | A/G | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132868459 | gtgagccgagatcgc[A/G]ccaccgcactccagc | 55743 |
rs12820026 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132874743 | GACCAGCACCCAGCG[C/T]GGGGAAGCCAGGCCC | 55743 |
rs12820068 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132844722 | tgcaacctccacctc[A/C]tgcgttcaactgatt | 55743 |
rs12820237 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132874856 | ACCCAGTGCAGGGAA[C/G]CCAGGCCCTGGAACA | 55743 |
rs12820251 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132874879 | CTGGAACAGGCGGGA[A/C]TGCCCAGGACCAGCA | 55743 |
rs12821394 | snp | G/T | 0.409721 | 0.192325 | intron-variant | CHFR | GRCh38.p7 | 12:132879005 | TTTTTTTTTGTTTTT[G/T]TTTGTTTTTTTTTTT | 55743 |
rs12821502 | snp | A/G | 0.378372 | 0.214524 | intron-variant | CHFR | GRCh38.p7 | 12:132870609 | AGGCTGCAGTGAGCT[A/G]AGATCGCGCCACCGC | 55743 |
rs12822599 | snp | C/T | 0.377977 | 0.21476 | intron-variant | CHFR | GRCh38.p7 | 12:132871308 | AATACAAAAATTAGC[C/T]GGGTGTGGTGGTGTG | 55743 |
rs12822648 | snp | A/G | 0.386694 | 0.20932 | intron-variant | CHFR | GRCh38.p7 | 12:132879636 | CCTCGTGATATGCCC[A/G]CCTCGGCTTCTCAAA | 55743 |
rs12822949 | snp | A/G | 0.377385 | 0.215112 | intron-variant | CHFR | GRCh38.p7 | 12:132856905 | GGGTGCTGGTGGAGG[A/G]ACCGCCCTCACTTGT | 55743 |
rs12823860 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132868347 | TACAAAAAATTAGCC[A/G]GGCGTGGTGACGGGT | 55743 |
rs12824499 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | CHFR | GRCh38.p7 | 12:132869260 | ggggaaggggacatg[G/T]ggagtcactgctggt | 55743 |
rs12824670 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132874639 | CCAGCACCCAGCGCG[A/G]GGAAGCCAGGCCCCG | 55743 |
rs12824695 | snp | C/T | 0.046775 | 0.145601 | upstream-variant-2KB | CHFR | GRCh38.p7 | 12:132889165 | gatgacagcacatgc[C/T]tatagtcccagctat | 55743 |
rs12825101 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132874803 | ACCCAGCGTGGGGAA[C/G]CCAGGCCCTGGAACA | 55743 |
rs12825296 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132874901 | GGACCAGCACCCAGC[A/G]CGGGGAAGCCAGGCC | 55743 |
rs12825913 | snp | G/T | | | downstream-variant-500B | CHFR | GRCh38.p7 | 12:132839852 | ACTCGGGATCTCCCC[G/T]CTCAGCCTCGCCCCT | 55743 |
rs12825925 | snp | A/T | | | downstream-variant-500B | CHFR | GRCh38.p7 | 12:132839872 | GCCTCGCCCCTGCAC[A/T]AACTTGGGACCTCCC | 55743 |
rs12826056 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132877896 | caagctccgcctccc[A/G]ggttcacaccattct | 55743 |
rs12826066 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132877904 | gcctcccaggttcac[A/G]ccattctcctgcctc | 55743 |
rs12826076 | snp | A/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132877927 | cctgcctcagcctcc[A/T]gagtagctgggactg | 55743 |
rs12826511 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132877942 | agagtagctgggact[A/G]caggcgcccgccatc | 55743 |
rs12827323 | snp | A/G | 0.325799 | 0.238232 | intron-variant | CHFR | GRCh38.p7 | 12:132878384 | tgaggcaggagaatc[A/G]catgaacccaggagg | 55743 |
rs12827944 | snp | A/G | 0.386694 | 0.20932 | intron-variant | CHFR | GRCh38.p7 | 12:132878692 | ggcgtggtggcgggc[A/G]ccttgtaatcccagc | 55743 |
rs12828130 | snp | A/G | 0.386694 | 0.20932 | intron-variant | CHFR | GRCh38.p7 | 12:132878745 | gaatggcgagaaccc[A/G]ggaggaggagcttgc | 55743 |
rs12829047 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132874588 | AGCACCCAGCGTGGG[A/G]AAGCCAGGCCCCAGA | 55743 |
rs12829062 | snp | A/G | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132874601 | GGAAAGCCAGGCCCC[A/G]GAACAGGCGGGACTG | 55743 |
rs12829278 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132874692 | CCAGCACCCAGCGCG[A/G]GGAAGCCAGGCCCCG | 55743 |
rs12829473 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132874775 | GGAACAGGCGGGACT[A/G]CCCAGGACCAGCACC | 55743 |
rs12829653 | snp | C/G | 0.391769 | 0.205917 | intron-variant | CHFR | GRCh38.p7 | 12:132880709 | tggtggctcacacct[C/G]taatctcagcacgtt | 55743 |
rs12829662 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132874850 | ACCAGCACCCAGTGC[A/G]GGGAACCCAGGCCCT | 55743 |
rs12829790 | snp | A/G | 0.046775 | 0.145601 | upstream-variant-2KB | CHFR | GRCh38.p7 | 12:132889211 | gggcagattccttga[A/G]cccgggaggacaagg | 55743 |
rs12830072 | snp | C/T | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132868480 | gcactccagcctggg[C/T]gacagagcgagactc | 55743 |
rs12830114 | snp | A/G | 0.393065 | 0.205018 | intron-variant | CHFR | GRCh38.p7 | 12:132880922 | gtgagccgagatcac[A/G]ccactgcactccagc | 55743 |
rs12830230 | snp | C/G | 0.330482 | 0.236691 | upstream-variant-2KB | CHFR | GRCh38.p7 | 12:132889388 | aactctttcaaccaa[C/G]tgccaatcagaaaat | 55743 |
rs12830262 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132874981 | GGCCCTGATGTAGGC[A/G]GGAAAGCCCAGGACC | 55743 |
rs12831326 | snp | C/T | 0.377187 | 0.215229 | intron-variant | CHFR | GRCh38.p7 | 12:132858816 | AGGCATAGTGGTGTG[C/T]ACCTGTAGTCCCAGC | 55743 |
rs12831415 | snp | C/T | 0.391583 | 0.206044 | intron-variant | CHFR | GRCh38.p7 | 12:132881724 | tacaaaaaaattagc[C/T]gggcatggtggcacg | 55743 |
rs12831987 | snp | C/G | 0.391024 | 0.206427 | intron-variant | CHFR | GRCh38.p7 | 12:132884313 | aatcccagctactcg[C/G]gaggctgaggcagga | 55743 |
rs12832132 | snp | A/G | 0.387074 | 0.209071 | intron-variant | CHFR | GRCh38.p7 | 12:132875897 | tgaaaaaagctggcc[A/G]ggcgcgatggctcac | 55743 |
rs12832244 | snp | C/T | 0.377977 | 0.21476 | intron-variant | CHFR | GRCh38.p7 | 12:132870656 | CAGAGCGAGACTCCA[C/T]CTCAAAACACAAAAG | 55743 |
rs12832467 | snp | A/G | 0.0704125 | 0.17392 | intron-variant | CHFR | GRCh38.p7 | 12:132862860 | gctgggattaaaggc[A/G]tgagccactgtgcct | 55743 |
rs28372675 | snp | C/T | 0.399073 | 0.200692 | upstream-variant-2KB, intron-variant | CHFR, LOC101928530 | GRCh38.p7 | 12:132888083 | TTCAGAACAGGAAGA[C/T]CCCGCAAAACGCCGG | 55743 |
rs28441991 | snp | C/T | 0.319616 | 0.240112 | intron-variant | CHFR | GRCh38.p7 | 12:132866070 | GAGGCTCTGAGAAGC[C/T]GGGGTTGTGTTTAGT | 55743 |
rs28495242 | snp | A/G | 0.244205 | 0.249933 | intron-variant | CHFR | GRCh38.p7 | 12:132871218 | GCACTCTGGGAGGCC[A/G]AGGCGGGCGGATTAC | 55743 |
rs28531371 | snp | A/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132845473 | AAAAAAAAAAATAAA[A/T]AAATAAATAAAAATA | 55743 |
rs28563944 | snp | C/T | 0.243633 | 0.249919 | intron-variant | CHFR | GRCh38.p7 | 12:132857107 | GGTGGAGGGACAGCC[C/T]TCACGTGCCCGGGTG | 55743 |
rs28718649 | snp | A/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132845481 | AAATAAATAAATAAA[A/T]AAAAATAAAAAAACT | 55743 |
rs34009587 | in-del | -/A | | | intron-variant | CHFR | GRCh38.p7 | 12:132881258 | CAAAAAAAAAAAAAA[-/A]GTAAAAATCTGTTCT | 55743 |
rs34182770 | in-del | -/T | 0.243919 | 0.249926 | intron-variant | CHFR | GRCh38.p7 | 12:132860281 | GTCCTGAGACACCCC[-/T]GCCAACATTACATTA | 55743 |
rs34220055 | snp | C/T | 0.00292801 | 0.0381501 | missense | CHFR | GRCh38.p7 | 12:132861611 | GGTGGTGGCATCTCC[C/T]CTAAAGGAAGTGGTC | 55743 |
rs34287227 | snp | C/T | 0.109108 | 0.206518 | intron-variant | CHFR | GRCh38.p7 | 12:132881589 | ATACTGACCACGGGC[C/T]GGGCACGGTGGCTCA | 55743 |
rs34347780 | in-del | -/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132845787 | GTCCCCGAGGGTCCC[-/C]AGGACAACTGACCCC | 55743 |
rs34376583 | in-del | -/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132885271 | ATACCACTGCCAGGC[-/C]GTGGTGGTGGGCGCC | 55743 |
rs34378203 | snp | A/G | 0 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132858754 | AAAAAAAAAAAAAAA[A/G]GGAATAAAAAATATT | 55743 |
rs34394151 | in-del | -/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132846996 | CGCAGGCACAGCCCT[-/G]GGACACTCACATGCG | 55743 |
rs34409499 | in-del | -/C | | | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132840934 | TTTTTTAATAAACAG[-/C]AAGCATATGCTTATT | 55743 |
rs34435580 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | CHFR | GRCh38.p7 | 12:132855999 | GCCTGGTGATGGTGC[C/T]TCTTCTGTAATAACG | 55743 |
rs34442791 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132869143 | GGGGAAGGGGACATG[C/G]GGAGTGACTGCTGGT | 55743 |
rs34510243 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132869196 | GGGGAGTGACTGCTG[C/G]TGGGGCCGAGGGGAA | 55743 |
rs34582981 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | CHFR | GRCh38.p7 | 12:132889527 | GTCAGGCCTCTGAAC[C/T]TAAGCTAAGCCATCG | 55743 |
rs34600455 | snp | A/G | 0.322245 | 0.239334 | intron-variant | CHFR | GRCh38.p7 | 12:132873448 | ATGCGGTTTTGAGCT[A/G]TGCAGATGCACTTAT | 55743 |
rs34632423 | multinucleotide-polymorphism | CA/TG | | | intron-variant | CHFR | GRCh38.p7 | 12:132873744 | TACGGGGCTAGAGTG[CA/TG]CACGGACTTGGGTGC | 55743 |
rs34636431 | in-del | -/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132885036 | AAGTTGCAGTGAGCC[-/C]GAGATCATGCCACTG | 55743 |
rs34663244 | multinucleotide-polymorphism | AC/GT | | | intron-variant | CHFR | GRCh38.p7 | 12:132874954 | GGACCAGCACCCAGC[AC/GT]GGGGAAGCCAGGCCC | 55743 |
rs34686024 | in-del | -/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132845285 | TGGTGAAACCTCACC[-/C]TCTACTAAAAATACA | 55743 |
rs34739714 | snp | A/G | 0.377385 | 0.215112 | intron-variant | CHFR | GRCh38.p7 | 12:132871223 | CTGGGAGGCCGAGGC[A/G]GGCGGATTACCTGAG | 55743 |
rs34753654 | in-del | -/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132856811 | GTGCTGGTGTGGATG[-/C]CCCTCACGTGCCCGG | 55743 |
rs34780016 | in-del | -/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132871658 | CACCTATAATCCCAG[-/G]CTACTCGGGAGGCTG | 55743 |
rs34840041 | in-del | -/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132853125 | TCTGGCAAACCCACT[-/G]GGGGGACATCAGCTG | 55743 |
rs35011845 | snp | A/C | 0.353411 | 0.22761 | synonymous-codon | CHFR | GRCh38.p7 | 12:132859130 | AGCGGCTGGGAAGCC[A/C]GACAAGATGGAGGAG | 55743 |
rs35051613 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132868956 | GGACATGGGGAGTGA[C/T]TGCTGGTGGGGCCGA | 55743 |
rs35061960 | in-del | -/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132856288 | CTGCCACGCCTCTCA[-/G]GGGGAGGTGCTAATA | 55743 |
rs35080377 | in-del | -/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132843699 | GGCCGAGCGTGGTGG[-/G]CTCATGCCTGCAATC | 55743 |
rs35090182 | in-del | -/A | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132855243 | CGAGACTTTGTCTCG[-/A]AAAAAAAAAAAAAAG | 55743 |
rs35090417 | snp | C/G | 0.319616 | 0.240112 | intron-variant | CHFR | GRCh38.p7 | 12:132867872 | ACTGTCAATTCTCCC[C/G]AAATCAAAAATCTCA | 55743 |
rs35095156 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132869202 | TGACTGCTGGTGGGG[C/T]CGAGGGGAAGGGGAC | 55743 |
rs35167652 | in-del | -/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132853725 | CATTCCTGTCCAGCA[-/C]CCCCAGTGTTAGAGA | 55743 |
rs35177584 | in-del | -/AA | | | intron-variant | CHFR | GRCh38.p7 | 12:132842127 | AAAAAAAAAAAAAAA[-/AA]GAAGTGCAAACATCT | 55743 |
rs35206714 | snp | C/T | 0.027392 | 0.113779 | missense | CHFR | GRCh38.p7 | 12:132861554 | AGCTTTGCCTCAGCT[C/T]TCCCAGACAGAAAGA | 55743 |
rs35207999 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132869182 | GGGGAAGGGGACATG[C/G]GGAGTGACTGCTGGT | 55743 |
rs35241589 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132862059 | AAGTGGATCACCTGA[A/G]GTCAGGAGGTCGAGA | 55743 |
rs35245349 | in-del | -/TAAAA | 0.386313 | 0.209568 | intron-variant | CHFR | GRCh38.p7 | 12:132845081 | TTTAAACATCAAAAT[-/TAAAA]TAAATACAACAAAAG | 55743 |
rs35290169 | in-del | -/T | 0.244205 | 0.249933 | intron-variant | CHFR | GRCh38.p7 | 12:132855854 | TAAAAGTTTCAAGTG[-/T]TTTTTTTTGTCGTTC | 55743 |
rs35297020 | snp | A/G | 0.394316 | 0.206983 | intron-variant | CHFR | GRCh38.p7 | 12:132884981 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 55743 |
rs35363071 | in-del | -/GAA | | | intron-variant | CHFR | GRCh38.p7 | 12:132864472 | GGCATACAGATAGAA[-/GAA]TTTTTATTTTTTATT | 55743 |
rs35407274 | in-del | -/TG | | | intron-variant | CHFR | GRCh38.p7 | 12:132885273 | ACCACTGCCAGGCGT[-/TG]GGTGGTGGGCGCCTG | 55743 |
rs35426930 | in-del | -/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132843321 | TCCCAGCACTTTGGG[-/G]AGGCAGAGGCAGGAG | 55743 |
rs35631975 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | CHFR | GRCh38.p7 | 12:132846920 | CAACCTGAAAGCATC[A/G]GGATCTTTTTCCTCT | 55743 |
rs35689228 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132869164 | GACTGCTGGTGGGGC[C/T]GAGGGGAAGGGGACA | 55743 |
rs35855109 | in-del | -/T | 0.297382 | 0.245469 | intron-variant | CHFR | GRCh38.p7 | 12:132849599 | ACATATTCAGGTGGC[-/T]TTTTTTTTTTTTTTG | 55743 |
rs35932270 | in-del | -/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132879586 | AGTAGAGATGAGGTT[-/T]CACAATGTTGGCCAG | 55743 |
rs36039891 | in-del | -/T | | | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132841113 | CAGCAGCAGGATATT[-/T]GTGTACGTCCTGTAG | 55743 |
rs36052883 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132869157 | GCGGAGTGACTGCTG[C/G]TGGGGCCGAGGGGAA | 55743 |
rs55724178 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132868409 | CAGGAAAATGGCGTG[A/G]ACCCAGGAGAATGGC | 55743 |
rs55784049 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132868383 | TAGTCCCAGCTACTC[A/G]GAGGCTGAGGCAGGA | 55743 |
rs55826641 | in-del | -/ATATATATATATAT | | | intron-variant | CHFR | GRCh38.p7 | 12:132850985 | TATATATATATATAT[-/ATATATATATATAT]GTTTTGTTTTGAGAC | 55743 |
rs55852696 | snp | A/G | 0.245916 | 0.249967 | intron-variant | CHFR | GRCh38.p7 | 12:132876182 | CCATCTCAAAAAAAA[A/G]AAAGAAAGAAAGAAA | 55743 |
rs55939852 | snp | A/C | 0.24449 | 0.249939 | intron-variant | CHFR | GRCh38.p7 | 12:132868683 | AGACTCCGTCTCAAC[A/C]ACAACAAAAAAGAGC | 55743 |
rs55996389 | snp | A/C | 0.0023933 | 0.0345097 | downstream-variant-500B | CHFR | GRCh38.p7 | 12:132840333 | AGGCAGCCCCAGACA[A/C]GAGCCCAACACGAGA | 55743 |
rs56065768 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132868399 | GAGGCTGAGGCAGGA[A/G]AATGGCGTGGACCCA | 55743 |
rs56163129 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132863471 | GTTCGCGCCATTGCA[C/T]TCCAGCCTGGGCAGT | 55743 |
rs56197652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132863448 | GAGGCGGAGTTGCAG[C/T]GAACGAAGTTCGCGC | 55743 |
rs56214606 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132863466 | ACGAAGTTCGCGCCA[C/T]TGCACTCCAGCCTGG | 55743 |
rs56223638 | in-del | -/A | 0.245061 | 0.249951 | intron-variant | CHFR | GRCh38.p7 | 12:132855510 | AAAAATACAAAAAAA[-/A]TTAGCTGGGTGTGGT | 55743 |
rs56233531 | snp | A/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132845486 | AATAAATAAATAAAA[A/T]TAAAAAAACTAAGAT | 55743 |
rs56322519 | in-del | -/G | 0.24449 | 0.249939 | intron-variant | CHFR | GRCh38.p7 | 12:132852519 | CACAGGAAAGACCCT[-/G]GCGAGGTCAACATGC | 55743 |
rs56720942 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132868726 | ATGTCTGTGAAGTGT[C/T]TAGAACAGAAAAATC | 55743 |
rs56915730 | snp | C/T | 0.0652144 | 0.168387 | intron-variant | CHFR | GRCh38.p7 | 12:132844755 | CCTGTCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 55743 |
rs56957418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132863452 | CGGAGTTGCAGCGAA[C/T]GAAGTTCGCGCCATT | 55743 |
rs57008057 | snp | A/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132872611 | ACAGCCTAACCAGCC[A/T]CTACACCTCCTCACG | 55743 |
rs57027326 | in-del | -/AA | 0.341685 | 0.232581 | intron-variant | CHFR | GRCh38.p7 | 12:132881887 | AAAAAAAAAAAAAAA[-/AA]GACTGACCACCTACA | 55743 |
rs57154544 | in-del | -/CTTCTCAGCCTTGCCCCTGCACTAACTCGGGACCTCCC | 0 | 0 | downstream-variant-500B | CHFR | GRCh38.p7 | 12:132839960 | AACTCGGGACCTCCC[lengthTooLong]TGCTCAGCCTCGCCC | 55743 |
rs57325276 | snp | G/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132854634 | ACACGGTGAAACCCA[G/T]TCTCTACCAAAAATA | 55743 |
rs57466534 | snp | A/G | | | downstream-variant-500B | CHFR | GRCh38.p7 | 12:132840046 | TCCCCTCCCGGCCTC[A/G]CCCCTGCACTAACAC | 55743 |
rs57498792 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132869007 | TGACTGCTGCTGGGG[C/T]TGAGGGGAAGGGGAC | 55743 |
rs57560560 | in-del | -/T | 0 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132865677 | TTTTTTTTTTTTTTT[-/T]GAGATGGGCTCTGGC | 55743 |
rs57575342 | snp | G/T | 0.0505692 | 0.150756 | intron-variant | CHFR | GRCh38.p7 | 12:132849638 | TCTTGCTCTGTGGCC[G/T]AGGCTGGAGTATAGT | 55743 |
rs57628324 | in-del | -/ATATATATAT | | | intron-variant | CHFR | GRCh38.p7 | 12:132850989 | TATATATATATATAT[-/ATATATATAT]GTTTTGTTTTGAGAC | 55743 |
rs58162770 | in-del | -/A | | | intron-variant | CHFR | GRCh38.p7 | 12:132868530 | AAAAACAAAAAAAAA[-/A]TTAGCTGGGCGTGGT | 55743 |
rs58793699 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132868948 | GGGGAAGGGGACATG[C/G]GGAGTGATTGCTGGT | 55743 |
rs58886285 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132880665 | TCCGACTCAAAAAAA[A/G]AAAAAAAAAGTCAAT | 55743 |
rs58994121 | in-del | -/A | | | intron-variant | CHFR | GRCh38.p7 | 12:132842128 | AAAAAAAAAAAAAAA[-/A]GAAGTGCAAACATCT | 55743 |
rs59054763 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132868917 | GGACATGGGGAGTGA[C/T]TGCTGGTGGGGCCGA | 55743 |
rs59069839 | in-del | -/AA/AAAT | 0 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132885457 | AATAAATAAATAAAT[-/AA/AAAT]TTCTGTTGCTTAAGC | 55743 |
rs59320699 | snp | C/G | 0.00358779 | 0.0422022 | upstream-variant-2KB, nc-transcript-variant | CHFR, LOC101928530 | GRCh38.p7 | 12:132888327 | TAAGAGGGTGAAGCA[C/G]GACCGGGCGCAGTGA | 55743 |
rs59464890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132859762 | AGTATTTAGAAGAAG[C/T]CAGGTGCAATGGCTC | 55743 |
rs59590453 | in-del | -/CAAA | | | intron-variant | CHFR | GRCh38.p7 | 12:132868517 | AAACAAACAAACAAA[-/CAAA]AAACAAAAAAAAATT | 55743 |
rs59602577 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132868969 | GATTGCTGGTGGGGC[C/T]GAGGGGAAGGGGACA | 55743 |
rs59632089 | snp | C/T | 0.116838 | 0.211584 | intron-variant | CHFR | GRCh38.p7 | 12:132866564 | ACACCGCGATTGTTA[C/T]AACACACCAGAATGT | 55743 |
rs59775768 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132869008 | GACTGCTGCTGGGGC[C/T]GAGGGGAAGGGGACA | 55743 |
rs60054929 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132840839 | CCAGGCTCGGGGCCG[C/T]GGTCACTCACCGGTT | 55743 |
rs60105558 | snp | C/G | 0.24019 | 0.249807 | intron-variant | CHFR | GRCh38.p7 | 12:132868479 | CGCACTCCAGCCTGG[C/G]TGACAGAGCGAGACT | 55743 |
rs60137048 | in-del | -/A | 0.375 | 0.216506 | intron-variant | CHFR | GRCh38.p7 | 12:132858754 | AAAAAAAAAAAAAAA[-/A]GGAATAAAAAATATT | 55743 |
rs60162679 | in-del | -/T | 0.236724 | 0.249647 | intron-variant | CHFR | GRCh38.p7 | 12:132845467 | ATCTCAAAAAAAAAA[-/T]ATAAATAAATAAATA | 55743 |
rs60360004 | snp | A/T | | | downstream-variant-500B | CHFR | GRCh38.p7 | 12:132840019 | GCCTCGCCCCTACAC[A/T]AACTCGGGACCTCCC | 55743 |
rs60471631 | snp | G/T | 0.499631 | 0.0135733 | downstream-variant-500B | CHFR | GRCh38.p7 | 12:132839962 | ACTCGGGACCTCCCT[G/T]CTCAGCCTCGCCCCT | 55743 |
rs60517452 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132868962 | GGGGAGTGATTGCTG[C/G]TGGGGCCGAGGGGAA | 55743 |
rs60875034 | in-del | -/A | | | intron-variant | CHFR | GRCh38.p7 | 12:132864187 | TTTGAAAAAAAAAAA[-/A]CACAAGAAACTGGCT | 55743 |
rs60941050 | snp | A/G | | | downstream-variant-500B | CHFR | GRCh38.p7 | 12:132840015 | CTCAGCCTCGCCCCT[A/G]CACAAACTCGGGACC | 55743 |
rs61083084 | in-del | -/A | 0 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132876174 | CTCAAAAAAAAAAAA[-/A]GAAAGAAAGAAAAAA | 55743 |
rs61412200 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132853596 | GAAGCACAGGGCCGA[A/G]CTGTGTGCAGGCCCC | 55743 |
rs61466030 | snp | C/T | 0.5 | 0 | downstream-variant-500B | CHFR | GRCh38.p7 | 12:132839971 | CTCCCTGCTCAGCCT[C/T]GCCCCTGCACTAACT | 55743 |
rs61625489 | snp | A/C | 0.243919 | 0.249926 | intron-variant | CHFR | GRCh38.p7 | 12:132866419 | GGAACACCACACCGG[A/C]ATGTTACAACACACC | 55743 |
rs61951562 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | CHFR | GRCh38.p7 | 12:132889276 | AGCCTGGGCAACAGA[A/G]ACCCTGTCAAAAAAA | 55743 |
rs61952802 | snp | C/T | 0.243919 | 0.249926 | intron-variant | CHFR | GRCh38.p7 | 12:132846242 | TGCTGGAATATGTCA[C/T]ACAGGTTCATGCTTA | 55743 |
rs61952804 | snp | C/T | 0.23846 | 0.249734 | intron-variant | CHFR | GRCh38.p7 | 12:132859913 | AGCCAGCTATGGTAG[C/T]GTGCACCTGTGGTCT | 55743 |
rs61952805 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CHFR | GRCh38.p7 | 12:132863602 | CATAGCTTCCAACGG[A/G]TGGAGATGGTGCTGC | 55743 |
rs61952806 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132864190 | TGAAAAAAAAAAACA[A/C]AAGAAACTGGCTTAC | 55743 |
rs61952807 | snp | A/G | 0.228253 | 0.249052 | intron-variant | CHFR | GRCh38.p7 | 12:132866907 | GTGGTGGTGGTGCGC[A/G]CCTGTGACCCCAGCT | 55743 |
rs61952810 | snp | A/T | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132877802 | AAGAAAGACATAAAG[A/T]AATTTTTTTTTTTTT | 55743 |
rs61952811 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | CHFR | GRCh38.p7 | 12:132879353 | ACAGGGATGCATCTA[C/T]AGCTGAATACAGTAA | 55743 |
rs61952827 | snp | G/T | 0.239902 | 0.249796 | intron-variant | CHFR | GRCh38.p7 | 12:132881196 | CATGGGAGGTGGAGG[G/T]TGCAGTGAGCTGAGA | 55743 |
rs61952828 | snp | C/T | 0.391024 | 0.206427 | intron-variant | CHFR | GRCh38.p7 | 12:132882929 | CTGGTCTCAAACTCA[C/T]AGGGTCAAGAGATCC | 55743 |
rs66746091 | snp | A/C | 0.239614 | 0.249784 | intron-variant | CHFR | GRCh38.p7 | 12:132842507 | GAACTCCTTGGGCCA[A/C]AGGAGTGATTTACGT | 55743 |
rs66881773 | in-del | -/C | 0.499631 | 0.0135733 | downstream-variant-500B | CHFR | GRCh38.p7 | 12:132839957 | ACTAACTCGGGACCT[-/C]TCCCTGCTCAGCCTC | 55743 |
rs67221706 | in-del | -/TATAGAG | 0.381113 | 0.21286 | intron-variant | CHFR | GRCh38.p7 | 12:132842068 | TCTGCCAGGCTGGAG[-/TATAGAG]GTGTGATCTCAGCTG | 55743 |
rs67642206 | snp | A/G | 0.47934 | 0.0995154 | intron-variant | CHFR | GRCh38.p7 | 12:132846380 | CCATTCTCCTTCCTC[A/G]GCCTCCCGAGTAGCT | 55743 |
rs67843035 | in-del | -/AA | 0.368529 | 0.220116 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886375 | GGGGTGAAATTAACC[-/AA]AAAAAAAAAAAAAAT | 55743 |
rs68159019 | snp | C/G | 0.379746 | 0.213696 | intron-variant | CHFR | GRCh38.p7 | 12:132846302 | GAGTCTCGCTCTGTC[C/G]CCCAGGCTGGAGTGC | 55743 |
rs71079144 | in-del | -/ATAT | 0 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132850995 | GTCTCAAAACAAAAC[-/ATAT]ATATATATATATATA | 55743 |
rs71079147 | in-del | -/CATGTCCCCTTCCCCTCGGCCCCACCAGCAGTCACTCCC | 0 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132869259 | CCAGCAGTGACTCCA[lengthTooLong]CATGTCCCCTTCCCC | 55743 |
rs71079148 | in-del | -/A | 0 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132879022 | GCGAGACTCCATCTC[-/A]AAAAAAAAAAAACAA | 55743 |
rs71452541 | snp | C/T | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132858724 | AGAGCGAGACTCCAT[C/T]TAAAAAAAAAAAAAA | 55743 |
rs71452542 | snp | A/G | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132858838 | AGTCCCAGCAACTCA[A/G]AAGGCTGAGGTCAGA | 55743 |
rs71452543 | snp | C/T | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132866910 | GTGGTGGTGCGCGCC[C/T]GTGACCCCAGCTACT | 55743 |
rs71452544 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | CHFR | GRCh38.p7 | 12:132873612 | GCTGGACTGACTTTC[C/T]GTGTCCTCCTGCTCC | 55743 |
rs71994478 | in-del | -/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132867958 | GAATAGCTAAGAAAA[-/T]TAAAAAAAAATAATA | 55743 |
rs72624275 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | CHFR | GRCh38.p7 | 12:132861910 | TTAGCCCTCGAGCAC[C/T]GAGTCTAACGCAGGG | 55743 |
rs73157075 | snp | A/T | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132866595 | TACAACACACCAGAA[A/T]GTTACAACACACCAG | 55743 |
rs73489148 | snp | A/C/G | 0.004783 | 0.0487016 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132840671 | GCAGCATGAGGGAGC[A/C/G]GCGCGTCCTGGGACC | 55743 |
rs73489155 | snp | C/T | 0.386313 | 0.209568 | intron-variant | CHFR | GRCh38.p7 | 12:132846476 | AGGGTTTTACCGTGT[C/T]AGCCAGGATGGTCTC | 55743 |
rs73489162 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CHFR | GRCh38.p7 | 12:132852815 | CAGGCCAGTGGCCTC[A/G]TGATGTGCTCAGCCC | 55743 |
rs74543332 | snp | A/G | 0.00180294 | 0.0299703 | intron-variant | CHFR | GRCh38.p7 | 12:132851770 | TCAGCCGGAGCACGT[A/G]GGACCCAGGGCAGAA | 55743 |
rs74544670 | snp | C/G | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132862092 | AGCCTGGCCAACATG[C/G]TGAAACCCCATCTCT | 55743 |
rs74613650 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CHFR | GRCh38.p7 | 12:132842894 | CTAAATGAAGATACC[A/G]GTTCCTAAAGGATGC | 55743 |
rs74828084 | snp | C/T | 0.0130937 | 0.0798461 | intron-variant | CHFR | GRCh38.p7 | 12:132848761 | TACACGCACTCAGCG[C/T]TGAGGGCTGTCTCCA | 55743 |
rs74923714 | in-del | -/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132864188 | TTTGAAAAAAAAAAA[-/C]ACAAGAAACTGGCTT | 55743 |
rs74997048 | snp | C/T | 0.5 | 0 | downstream-variant-500B | CHFR | GRCh38.p7 | 12:132839928 | TTGGGACCTCCCCCT[C/T]AGCCTCGCCCCTGCA | 55743 |
rs75067639 | snp | A/C | 0.0722614 | 0.17581 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886339 | AAAAAACAAAAAAAA[A/C]CAGGTGCAAGCACAT | 55743 |
rs75167846 | snp | C/G | | | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132840725 | CCGTGGTCACTCACA[C/G]AAGGGAGCAGCACGT | 55743 |
rs75233493 | snp | C/T | 0.479583 | 0.0989539 | intron-variant | CHFR | GRCh38.p7 | 12:132846419 | AGGCGCCCGCCACCA[C/T]GCCCGGCTAATTTTT | 55743 |
rs75237791 | snp | A/G | 0.00914312 | 0.0669923 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132841280 | CTCGGCGGGACGGCC[A/G]CATGTTACAGAAAGG | 55743 |
rs75265771 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | CHFR | GRCh38.p7 | 12:132867848 | CACCATTTTCCTGGG[C/T]TCTGTAAAACTGTCA | 55743 |
rs75340219 | snp | A/G | 0.0644693 | 0.167566 | intron-variant | CHFR | GRCh38.p7 | 12:132841713 | GGAAACCATACACAG[A/G]AAGAGCTACCTGAGA | 55743 |
rs75391939 | snp | C/T | 0.0228546 | 0.104427 | synonymous-codon, intron-variant | CHFR | GRCh38.p7 | 12:132869659 | TGCAGGAGAAGGCTC[C/T]GTGGAAGAGGCCGAG | 55743 |
rs75449706 | snp | C/T | 0.115848 | 0.210958 | intron-variant | CHFR | GRCh38.p7 | 12:132859275 | CAAGAAGGAAATACA[C/T]GCAGGTTCAGGTCAA | 55743 |
rs75488281 | snp | A/G | 0.00438332 | 0.0466095 | upstream-variant-2KB, nc-transcript-variant | CHFR, LOC101928530 | GRCh38.p7 | 12:132887851 | GGAACTTCCGGATTG[A/G]AAGCCCCAAGGATTC | 55743 |
rs75550405 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132844310 | TTTTTATTGAGACGG[A/C]GTCTCGCTCTGTCGC | 55743 |
rs75731301 | snp | A/T | | | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886872 | CCACATATCTGTGAA[A/T]TTTCCACTTTTCCTT | 55743 |
rs75830925 | snp | C/T | 0.248755 | 0.249997 | intron-variant | CHFR | GRCh38.p7 | 12:132875483 | CCCATCTGAGCTAGG[C/T]GTGGCGGCGGGCACC | 55743 |
rs75921355 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132844298 | GATACGAATTTATTT[C/T]TATTGAGACGGAGTC | 55743 |
rs75992503 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | CHFR | GRCh38.p7 | 12:132882070 | AGCTAAGAGAAAAAT[C/G]TATGTCCCTACAAAG | 55743 |
rs76060528 | snp | A/G | 0.133777 | 0.221342 | intron-variant | CHFR | GRCh38.p7 | 12:132842454 | CTGAGTCCACACAAC[A/G]TCTCGTCCTGAGGGC | 55743 |
rs76224039 | snp | A/G | 1.66228e-05 | 0.0028829 | missense | CHFR | GRCh38.p7 | 12:132844030 | GGGGCTCCTTACCTG[A/G]CAACTCGGAAGCAGG | 55743 |
rs76242920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132848429 | TCTGTCCTGGGAGTA[C/T]CTCCCCTAATAATTC | 55743 |
rs76408131 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132885767 | GAAGTAGGTACATAG[A/G]CGCAGAAAGATGTCG | 55743 |
rs76562896 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132883070 | CACAGCATTTGCTGC[A/G]CTTGACGCTTGGTGG | 55743 |
rs76708933 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132844409 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 55743 |
rs76732780 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | CHFR | GRCh38.p7 | 12:132850759 | TGCACAGAGCAACAC[C/T]GGTGTGTGCGGCAGG | 55743 |
rs76751330 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | CHFR | GRCh38.p7 | 12:132863449 | AGGCGGAGTTGCAGC[A/G]AACGAAGTTCGCGCC | 55743 |
rs76832928 | snp | C/T | 0.0141495 | 0.0829129 | intron-variant | CHFR | GRCh38.p7 | 12:132841634 | TTACACAAGAGAGCA[C/T]TGGAGAGGCAATCAA | 55743 |
rs76946232 | snp | C/T | 0.0593499 | 0.161718 | intron-variant | CHFR | GRCh38.p7 | 12:132851595 | ATAGGAACCCGCCTG[C/T]GTGCGGTGGCGCGGG | 55743 |
rs77052806 | snp | C/T | | | missense | CHFR | GRCh38.p7 | 12:132877631 | CAGAGACCAGTTTAT[C/T]GCTGGGGAAGGAAAG | 55743 |
rs77149327 | snp | C/T | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132869085 | TGACTGCTGCTGGGG[C/T]CGAGGGGAAGGGGAC | 55743 |
rs77350630 | snp | C/T | 0.479583 | 0.0989539 | intron-variant | CHFR | GRCh38.p7 | 12:132846414 | ACTACAGGCGCCCGC[C/T]ACCACGCCCGGCTAA | 55743 |
rs77439977 | snp | C/T | 0.0670745 | 0.170406 | intron-variant | CHFR | GRCh38.p7 | 12:132882609 | TCCATTGAGCGTTAA[C/T]TGCCAGGACAGTCTC | 55743 |
rs77700489 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132860281 | GTCCTGAGACACCCC[C/T]GCCAACATTACATTA | 55743 |
rs77719222 | snp | A/G | 0.24449 | 0.249939 | intron-variant | CHFR | GRCh38.p7 | 12:132845571 | GAGATGATCTCTTGA[A/G]CCCAGGAGGTCGAGG | 55743 |
rs77770402 | snp | A/G | 0.482384 | 0.0921818 | intron-variant | CHFR | GRCh38.p7 | 12:132846412 | GGACTACAGGCGCCC[A/G]CCACCACGCCCGGCT | 55743 |
rs77850473 | snp | A/C | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132871772 | AGCGAAACTCTATCT[A/C]AAAAAAAAAAAAGTA | 55743 |
rs77912561 | snp | C/G | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132884039 | GCATGAGAATCGCTT[C/G]AACTCTAAAGGCGGA | 55743 |
rs77936594 | snp | A/G | 0.243633 | 0.249919 | intron-variant | CHFR | GRCh38.p7 | 12:132871805 | TCAGGGGTGACCTTC[A/G]AAGGACTCCCATAAC | 55743 |
rs78083828 | snp | C/T | 0.110167 | 0.207236 | intron-variant | CHFR | GRCh38.p7 | 12:132858948 | TGGGTGACAGAGTAA[C/T]CTCAGCAGATGCCAG | 55743 |
rs78109984 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132844300 | TACGAATTTATTTTT[A/C]TTGAGACGGAGTCTC | 55743 |
rs78156200 | snp | A/C | | | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886871 | TCCACATATCTGTGA[A/C]TTTTCCACTTTTCCT | 55743 |
rs78308059 | snp | A/G | 0.234109 | 0.249494 | intron-variant | CHFR | GRCh38.p7 | 12:132879892 | TCCTAAACGTTCCAC[A/G]CAGAAAGACACCCTG | 55743 |
rs78404449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132852574 | CACCCAGGTTCACTG[A/G]GCACCCACTGAGGGA | 55743 |
rs78410518 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | CHFR | GRCh38.p7 | 12:132841814 | AATTTTGAAACAGAA[A/G]TGCAAACATCTGGCC | 55743 |
rs78485138 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132869065 | GGGGAAGGGGACATG[C/G]GGAGTGACTGCTGCT | 55743 |
rs78550059 | snp | A/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132845085 | AACATCAAAATTAAA[A/T]TAAATACAACAAAAG | 55743 |
rs78593341 | snp | C/G | 0 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132884017 | CCCAGCTACTCGGGA[C/G]GCTGAGGCAGGAAAA | 55743 |
rs78615146 | snp | A/G | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132872566 | CTCACCATTCTCTCA[A/G]GAAATGGCTCGCCCA | 55743 |
rs78683606 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CHFR | GRCh38.p7 | 12:132867466 | TCCCTTCTCCGGAGG[C/T]TTCCTGGTGCCTGCC | 55743 |
rs78686884 | snp | A/T | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132845309 | AAATACAAAAAAAAA[A/T]TTAGCTGGGCATGTT | 55743 |
rs78901493 | snp | A/G | 0.245346 | 0.249957 | intron-variant | CHFR | GRCh38.p7 | 12:132885596 | AAAGATAAACTCAAC[A/G]ACATATTTTCTCTCC | 55743 |
rs78929140 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | CHFR | GRCh38.p7 | 12:132863701 | TATCTCCACGAGCAA[A/G]AAGCCAGAGTCATAA | 55743 |
rs79136624 | snp | G/T | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132878998 | ATTTGTTTTTTTTTT[G/T]GTTTTTGTTTGTTTT | 55743 |
rs79216723 | snp | A/C | 0.245061 | 0.249951 | intron-variant | CHFR | GRCh38.p7 | 12:132844627 | TCCCACGTGGATATA[A/C]CATTTATTTTATTTA | 55743 |
rs79242673 | snp | G/T | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132846277 | TCTTTTTTTTTTTTT[G/T]TTTGAGACGGAGTCT | 55743 |
rs79486443 | snp | G/T | 0.093417 | 0.194889 | intron-variant | CHFR | GRCh38.p7 | 12:132864115 | AATAAAGACTTAGTT[G/T]ATCATATTACAGCAT | 55743 |
rs79489794 | snp | C/T | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132859367 | GCAGTCTTTTTTTTT[C/T]CGAGACAGAGTCTCG | 55743 |
rs79504747 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CHFR | GRCh38.p7 | 12:132851551 | CCCTAAGGCCAACAC[C/T]GCTTTGAAACCTGAC | 55743 |
rs79546833 | snp | C/G/T | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132859368 | CAGTCTTTTTTTTTT[C/G/T]GAGACAGAGTCTCGC | 55743 |
rs79596794 | snp | A/G | 0 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132846281 | TTTTTTTTTTTTTTT[A/G]AGACGGAGTCTCGCT | 55743 |
rs79627296 | snp | A/T | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132877806 | AAGACATAAAGAAAT[A/T]TTTTTTTTTTTCTTG | 55743 |
rs79786051 | snp | C/T | 0.5 | 0 | downstream-variant-500B | CHFR | GRCh38.p7 | 12:132839934 | CCTCCCCCTTAGCCT[C/T]GCCCCTGCACTAACT | 55743 |
rs79793085 | snp | A/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886390 | AAAAAAAAAAAAAAA[A/T]TTGCTTCCAAACAGC | 55743 |
rs79942025 | snp | A/T | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132845311 | ATACAAAAAAAAAAT[A/T]AGCTGGGCATGTTGG | 55743 |
rs80032242 | snp | A/G | 0.128632 | 0.218563 | intron-variant | CHFR | GRCh38.p7 | 12:132874691 | ACCAGCACCCAGCGC[A/G]AGGAAGCCAGGCCCC | 55743 |
rs80126514 | snp | C/T | 1.68182e-05 | 0.00289979 | intron-variant | CHFR | GRCh38.p7 | 12:132861431 | TGCCCCAGGAGCACA[C/T]GAGAGGACTGAGGAC | 55743 |
rs80312391 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | CHFR | GRCh38.p7 | 12:132872226 | GAGGAACGTTCAGAG[A/G]GCGCCCTCACGTGCA | 55743 |
rs80327949 | snp | A/G | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132846282 | TTTTTTTTTTTTTTG[A/G]GACGGAGTCTCGCTC | 55743 |
rs111254085 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132849681 | GCTCACTGCAACCTC[C/T]GCCTCCTGGGTTCAA | 55743 |
rs111281460 | snp | A/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132883439 | CTCAAAAAAAAAAAA[A/T]AAAAGACTGGGCGCA | 55743 |
rs111338463 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132840705 | CTCCAGCCCTGGGCT[C/T]GGGGCCGTGGTCACT | 55743 |
rs111364734 | snp | A/G | 0.319856 | 0.240042 | intron-variant | CHFR | GRCh38.p7 | 12:132844816 | TTATACTTTTTTAGT[A/G]GAGATGGGGTTTCAC | 55743 |
rs111384368 | snp | A/G | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132857246 | TGCCCTCACGTGCCC[A/G]GGTGCTGGTGGAGGG | 55743 |
rs111391889 | snp | C/T | 0.5 | 0 | downstream-variant-500B | CHFR | GRCh38.p7 | 12:132839914 | ACCCCTGCACAAACT[C/T]GGGACCTCCCCCTTA | 55743 |
rs111393180 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | CHFR | GRCh38.p7 | 12:132850054 | TGCCTCCCGGGTTCA[C/T]GCCATTCTCCTGCCT | 55743 |
rs111472686 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132883536 | CAAGACCATCCTGGC[C/T]AACATGGTGAAACCC | 55743 |
rs111479711 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132862683 | CTCCTGGGTTGACGC[C/G]ATTCTCCTGCCTCAG | 55743 |
rs111633819 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132883161 | GGCTGGGCGCGGTGG[A/C]TCACACCTGTAATCC | 55743 |
rs111747038 | snp | C/T | 0.244776 | 0.249945 | intron-variant | CHFR | GRCh38.p7 | 12:132870257 | CTCGGGAGGCTGAGG[C/T]AGGAGAATGGCATGA | 55743 |
rs111769193 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132857301 | GGTGGAGGGACAGCC[C/T]TCACGTGCCCGGGTG | 55743 |
rs111772956 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | CHFR | GRCh38.p7 | 12:132863010 | CACGCCATTCTCCTG[C/T]CTCAGCCTCCTGAGT | 55743 |
rs111786421 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132840738 | CACAAGGGAGCAGCA[C/T]GTCCTGGGACCTGCG | 55743 |
rs111790907 | snp | C/T | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132868334 | TCTCTACTAAAAATA[C/T]AAAAAATTAGCCAGG | 55743 |
rs111792039 | snp | A/G | 0.320096 | 0.239972 | intron-variant | CHFR | GRCh38.p7 | 12:132846408 | GCTGGGACTACAGGC[A/G]CCCGCCACCACGCCC | 55743 |
rs111799372 | snp | A/G | | | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132840775 | CCCAGGCTCGGGGCC[A/G]CGGTCACTCACACAA | 55743 |
rs111820152 | snp | A/G | 0.5 | 0 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132841395 | GGTCTCACTCAGAGG[A/G]TAAAGCTCCACAGAA | 55743 |
rs111825998 | snp | A/G | 0 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132852235 | CCTTGTGATCCGCCC[A/G]CCTCGGCCTCCCAAA | 55743 |
rs111839026 | snp | A/G | 0.241053 | 0.24984 | intron-variant | CHFR | GRCh38.p7 | 12:132883422 | TAGGAGTGAAACTCC[A/G]TCTCAAAAAAAAAAA | 55743 |
rs111895859 | snp | C/T | 0.319376 | 0.240181 | intron-variant | CHFR | GRCh38.p7 | 12:132870276 | AGAATGGCATGAACC[C/T]GGGAGGTGGAGGTTG | 55743 |
rs111976343 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132880749 | AGGCGGGCGGATCAC[A/G]AGGTCAGGAGTTCAA | 55743 |
rs111999312 | snp | C/T | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132857215 | CCGCCCTCACGTGCC[C/T]GGGTGCTGGTGTGGA | 55743 |
rs112009161 | snp | G/T | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132859444 | CAAGCTCCGCCTCCC[G/T]GGTTCATGCCATTCT | 55743 |
rs112051151 | snp | C/T | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132847003 | CACAGCCCTGGACAC[C/T]CACATGCGCCTTAGA | 55743 |
rs112055726 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132860845 | GCAACCTCCACCTGC[C/T]GGGTTCAAGCAATTC | 55743 |
rs112080749 | snp | A/C | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132868510 | CCATCTCAAAACAAA[A/C]AAACAAAAAACAAAA | 55743 |
rs112083933 | snp | A/G | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132875171 | ATTAGACTAGGAAAC[A/G]GAGCATCAGTTCTTC | 55743 |
rs112088188 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132871102 | CTGGTTAAGTTTATG[C/T]TGAAGATGCCTAAGA | 55743 |
rs112112016 | snp | A/G | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132854793 | CCTGGGCAACAGAGC[A/G]AAACTCCATCTCAAA | 55743 |
rs112114186 | snp | A/G | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132860049 | GATCCTGTCTCTTAA[A/G]AAAATGTATACATAA | 55743 |
rs112132590 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CHFR | GRCh38.p7 | 12:132865195 | GGGCTGTCCCTGCAC[A/G]GGGAGAGTCAGTGCA | 55743 |
rs112286961 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132862781 | GAGACAGGGTTTCAC[C/T]GTGTTAGCCAGGATG | 55743 |
rs112336814 | snp | A/G | 0.245346 | 0.249957 | intron-variant | CHFR | GRCh38.p7 | 12:132862754 | CCAGCTAATTTTTTT[A/G]TATTTTTAGTAGAGA | 55743 |
rs112365212 | snp | C/G | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132882044 | CCCAGCAATTCCATT[C/G]ATAGTTACTTAGCTA | 55743 |
rs112381475 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132868634 | GCAGTGAGCCGAGAT[C/T]GCACCACTGCACTCC | 55743 |
rs112414883 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132842258 | CCTGTGGCCACCTTC[C/T]CTCTCCACAGACTGT | 55743 |
rs112509379 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | CHFR | GRCh38.p7 | 12:132877090 | GTGAGCCACCGCGCC[C/T]GGGCTGATAATAATG | 55743 |
rs112516147 | snp | A/C | 0 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132878146 | CTCAAAGACACCCAT[A/C]AATACCTCCAGTTAC | 55743 |
rs112570077 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | CHFR | GRCh38.p7 | 12:132862998 | GCCTCCCTGGTTCAC[A/G]CCATTCTCCTGCCTC | 55743 |
rs112581844 | snp | C/G | 0.0228947 | 0.104514 | upstream-variant-2KB | CHFR | GRCh38.p7 | 12:132889201 | AGGCTGAGGTGGGCA[C/G]ATTCCTTGAGCCCGG | 55743 |
rs112619536 | snp | A/G | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132856956 | CACCCTCGCTTGCCC[A/G]GGTGCTGGTGGAGGG | 55743 |
rs112627798 | snp | A/C/G | 0.0126979 | 0.078662 | intron-variant | CHFR | GRCh38.p7 | 12:132866627 | AAGTTACAACACACC[A/C/G]CGTAACACCAAATGT | 55743 |
rs112628569 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132857272 | GAGGGACCACCCTCA[C/T]GTGCCCGGGTGCTGG | 55743 |
rs112640341 | snp | A/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132870156 | AGGAGATCGAGGCCA[A/T]CCTGGCTAACACGGT | 55743 |
rs112673186 | snp | C/T | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132873702 | GCTGGACTGACTTTC[C/T]GTGTCCTCCTGCTCC | 55743 |
rs112837313 | snp | G/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132862990 | CAAGCTCTGCCTCCC[G/T]GGTTCACGCCATTCT | 55743 |
rs112863721 | snp | G/T | 0.0372196 | 0.131242 | intron-variant | CHFR | GRCh38.p7 | 12:132870570 | GAGACTGAAGCAGGG[G/T]AATTGCTTGAACCCA | 55743 |
rs112870346 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132841177 | TGTTTTTGATAAACT[C/T]GCCCTTCTCCCTTGA | 55743 |
rs112898402 | snp | G/T | 0.245346 | 0.249957 | intron-variant | CHFR | GRCh38.p7 | 12:132877981 | CTAATTTTTTGTGTT[G/T]TTAGTAGAGACGGGG | 55743 |
rs112903909 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | CHFR | GRCh38.p7 | 12:132877362 | AAGATGATCAAATTG[C/T]CTGACACATTTCTCA | 55743 |
rs112917792 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132852460 | TCGATGTGGCAGCAG[A/G]AGTCTGAGCCCACAC | 55743 |
rs112952410 | snp | A/G | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132870424 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 55743 |
rs112960453 | snp | A/G | 0.116838 | 0.211584 | intron-variant | CHFR | GRCh38.p7 | 12:132863054 | GGTGCCCGCCACCAC[A/G]CCCGGCTAATTTTTT | 55743 |
rs112971324 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | CHFR | GRCh38.p7 | 12:132868406 | AGGCAGGAAAATGGC[A/G]TGGACCCAGGAGAAT | 55743 |
rs112974471 | snp | A/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132864591 | CCTCCTGGGTTCAAG[A/T]GATTCTCATGCCTCA | 55743 |
rs113102875 | in-del | -/A | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132862279 | AAACTCCCTCTGGGG[-/A]AAAAAAAATAAAAAT | 55743 |
rs113109257 | snp | C/T | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132874902 | GACCAGCACCCAGCG[C/T]GGGGAAGCCAGGCCC | 55743 |
rs113157158 | snp | C/T | 0 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132868317 | AACACGGTGAAACTC[C/T]GTCTCTACTAAAAAT | 55743 |
rs113187907 | snp | A/G | 0.244205 | 0.249933 | intron-variant | CHFR | GRCh38.p7 | 12:132846294 | TTGAGACGGAGTCTC[A/G]CTCTGTCCCCCAGGC | 55743 |
rs113225866 | snp | A/G | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132856795 | TGCCCTCACGTGCCC[A/G]GGTGCTGGTGTGGAT | 55743 |
rs113262120 | snp | A/G | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132873648 | GCTGGCTACGGGGCT[A/G]GAGTGCACACGGACT | 55743 |
rs113272987 | snp | C/T | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132842773 | TGATGGGGTGTGCCC[C/T]GGATGCCTCAGACAA | 55743 |
rs113277971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132868701 | AACAAAAAAGAGCAC[A/G]CATGATTCCATGTCT | 55743 |
rs113284424 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132879133 | CCTCAGCCTCCTGAG[C/T]AGCTGGGACTACAGG | 55743 |
rs113311106 | snp | A/G | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132846868 | CTGGGCAACAAGAGC[A/G]AGACTCCATCTCAAA | 55743 |
rs113316546 | snp | A/G | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132849304 | TGATGCACTGCACCC[A/G]GCCTCAGACCCGTAT | 55743 |
rs113421205 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, nc-transcript-variant | CHFR, LOC101928530 | GRCh38.p7 | 12:132888140 | CACTTCTTGGAATCC[A/G]GCGGCGTTCACGTGT | 55743 |
rs113473501 | snp | C/T | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132856253 | ACCCCCTGGCTACCC[C/T]GCTAAGTGTTCACCC | 55743 |
rs113480277 | snp | A/G | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132875034 | GGCCCTGATGTAGGC[A/G]GGAAAGCCCAGGACC | 55743 |
rs113492159 | snp | A/G | 0.273049 | 0.248935 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132887383 | AGACTCCCGACCCCA[A/G]AGGCCGAGACTCGGC | 55743 |
rs113495299 | snp | C/T | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132862913 | TTTTCTTTTTCTTTT[C/T]TGAGACAGAGTCTCA | 55743 |
rs113511206 | snp | A/G | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132876986 | TTTTAAGAGAGACAG[A/G]GTTTCTCCATGTTGG | 55743 |
rs113549134 | in-del | -/G | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132872746 | CTGAGCTGGACTTGT[-/G]CTATCCACAGTTCTG | 55743 |
rs113596819 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132867213 | AAAACCACATCAACA[A/G]AAGTGGAAACAGGCC | 55743 |
rs113705017 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | CHFR | GRCh38.p7 | 12:132882976 | CAAACTGCTGGGATT[A/G]CAGGCATGAGCCACC | 55743 |
rs113796069 | snp | C/T | 0.245346 | 0.249957 | intron-variant | CHFR | GRCh38.p7 | 12:132858600 | GGGCATGGTGGCACA[C/T]GCCTGCAGTCCCAGC | 55743 |
rs113799585 | snp | A/G | 0.24449 | 0.249939 | intron-variant | CHFR | GRCh38.p7 | 12:132844547 | CCTCGGCCTCCCAAA[A/G]TGCTGGGATTACAGG | 55743 |
rs113800546 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132841511 | TTTAAAAACACGCTC[C/T]CTTCACCTCCAGTGC | 55743 |
rs113820033 | snp | A/G | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132875011 | CAGCACCCAGCGTGG[A/G]GAAGCCAGGCCCTGA | 55743 |
rs113924002 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CHFR | GRCh38.p7 | 12:132850015 | CTGGAGTGCACTGGC[A/G]CCATCTCGGCTCACT | 55743 |
rs113941471 | snp | A/C | 0.0390383 | 0.134146 | intron-variant, missense | CHFR | GRCh38.p7 | 12:132862399 | GGAGTTTTAGACCAG[A/C]CTGGGCAACACAGCA | 55743 |
rs113964739 | in-del | -/AC | 0.5 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132873748 | GGCTAGAGTGTGCAC[-/AC]GGACTTGGGTGCATG | 55743 |
rs114117795 | snp | A/G | 1.70566e-05 | 0.00292027 | missense | CHFR | GRCh38.p7 | 12:132851636 | GCTGAGGGGCGACAC[A/G]CGGGTCCTGCTCGCG | 55743 |
rs114252669 | snp | A/G | 0.0693013 | 0.172766 | intron-variant | CHFR | GRCh38.p7 | 12:132873795 | ATCCCCCCAGATGCC[A/G]AGGGGCGACTGCAGC | 55743 |
rs114294325 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132857776 | GAGTAGATTATGACT[G/T]CAGGAACACAAACAA | 55743 |
rs114464009 | snp | C/T | 0.00119028 | 0.0243665 | intron-variant | CHFR | GRCh38.p7 | 12:132869852 | GTAACCCAAAAGGAG[C/T]AGAAGCAGCACACAA | 55743 |
rs114480187 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CHFR | GRCh38.p7 | 12:132864297 | GGCCGGCCCCCAGCC[A/G]GCACCCACTCACGCC | 55743 |
rs114483951 | snp | C/T | 1.65551e-05 | 0.00287702 | missense | CHFR | GRCh38.p7 | 12:132844062 | ATGTTCTGCCGATAC[C/T]GATAGGTCAGCTCAC | 55743 |
rs114523680 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CHFR | GRCh38.p7 | 12:132866071 | AGGCTCTGAGAAGCC[A/G]GGGTTGTGTTTAGTC | 55743 |
rs114563396 | snp | C/G | 0.00755907 | 0.0610114 | upstream-variant-2KB | CHFR | GRCh38.p7 | 12:132889182 | ATAGTCCCAGCTATT[C/G]AGGAGGCTGAGGTGG | 55743 |
rs114959815 | snp | C/G | 0.0360663 | 0.129354 | intron-variant | CHFR | GRCh38.p7 | 12:132867120 | AAGGAGCGGATGCAA[C/G]AAGGCCTCAAGAACA | 55743 |
rs115004038 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | CHFR | GRCh38.p7 | 12:132863456 | GTTGCAGCGAACGAA[C/G]TTCGCGCCATTGCAC | 55743 |
rs115029653 | snp | A/G | 0.000429284 | 0.0146444 | synonymous-codon | CHFR | GRCh38.p7 | 12:132857472 | ACAGATCCGCTCCAC[A/G]GGACAGCGGCAGGTA | 55743 |
rs115096950 | snp | C/T | 0.0086777 | 0.0652958 | missense | CHFR | GRCh38.p7 | 12:132859207 | CGACCAACAACTGCC[C/T]GTTCAGGTCAAGGTC | 55743 |
rs115234810 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | CHFR | GRCh38.p7 | 12:132873459 | AGCTGTGCAGATGCA[C/T]TTATACACGGGTTTT | 55743 |
rs115351605 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | CHFR | GRCh38.p7 | 12:132850519 | TCAGCAGTGGCCAGC[A/G]CCTGCCGTGGATGAC | 55743 |
rs115354268 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | CHFR | GRCh38.p7 | 12:132874689 | GGACCAGCACCCAGC[A/G]CGAGGAAGCCAGGCC | 55743 |
rs115422003 | snp | C/G | 0.0528381 | 0.153711 | intron-variant | CHFR | GRCh38.p7 | 12:132868961 | TGGGGAGTGATTGCT[C/G]GTGGGGCCGAGGGGA | 55743 |
rs115431373 | snp | A/G | 0.000346606 | 0.0131599 | synonymous-codon | CHFR | GRCh38.p7 | 12:132859193 | TCTACGCGGTTGTGC[A/G]ACCAACAACTGCCCG | 55743 |
rs115442831 | snp | A/C | 0.0640965 | 0.167152 | intron-variant | CHFR | GRCh38.p7 | 12:132856976 | CTGGTGGAGGGACCA[A/C]CCTCACGTGCCCGGG | 55743 |
rs115551350 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | CHFR | GRCh38.p7 | 12:132851562 | ACACCGCTTTGAAAC[A/C]TGACCCCTGAAGGAC | 55743 |
rs115566777 | snp | A/G | 8.46532e-05 | 0.00650534 | synonymous-codon | CHFR | GRCh38.p7 | 12:132844112 | GCAGTAACACAGAAC[A/G]GTGTCTCCCGTGACT | 55743 |
rs115645765 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132872139 | ACAGACACTATTCAC[A/G]GCAGGAACCCATGTG | 55743 |
rs115684143 | snp | A/G | 0.00015512 | 0.00880546 | missense | CHFR | GRCh38.p7 | 12:132844122 | AGAACGGTGTCTCCC[A/G]TGACTCTGTAATCTG | 55743 |
rs115711908 | snp | C/T | 0.000151087 | 0.00869025 | synonymous-codon | CHFR | GRCh38.p7 | 12:132877569 | CCTGGTATCTTCCAG[C/T]GTCACCTGACCTGAT | 55743 |
rs115746430 | snp | C/T | 0.0711525 | 0.174681 | intron-variant | CHFR | GRCh38.p7 | 12:132866300 | AATGTGACAACACAC[C/T]GGAATGTTAACACAC | 55743 |
rs115769697 | snp | A/C/G | 0.0588605 | 0.161139 | intron-variant | CHFR | GRCh38.p7 | 12:132875098 | AGGCGGGACAGCTAG[A/C/G]GACCAGCACCCTGCC | 55743 |
rs115799873 | snp | A/G | 0.0111196 | 0.0737302 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132840883 | TAACTTGGCGGCCAC[A/G]TCGAGGGTTAGCAGT | 55743 |
rs115801822 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CHFR | GRCh38.p7 | 12:132867182 | TGAAGACAGAGCAAC[A/G]GCATACAACGGAGTA | 55743 |
rs115806118 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | CHFR | GRCh38.p7 | 12:132884719 | AGTGGCCACCTGCAA[C/G]CCAAGAGAGCCCTCA | 55743 |
rs115923354 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | CHFR | GRCh38.p7 | 12:132861778 | GTGGCTTACGAGGAG[C/T]GTGTGCTCACTCAAC | 55743 |
rs115972571 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CHFR | GRCh38.p7 | 12:132876677 | CTTAATTTGAATACA[C/T]TCAAGAAGGGTCATA | 55743 |
rs116138868 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CHFR | GRCh38.p7 | 12:132866437 | GTTACAACACACCCT[A/G]GAACGTTACAACACA | 55743 |
rs116286061 | snp | C/T | 0.00158116 | 0.0280727 | synonymous-codon | CHFR | GRCh38.p7 | 12:132851694 | GAAGCAGCAGGTGCA[C/T]AGGGCGTGGCTTCCT | 55743 |
rs116330402 | snp | C/G | 0.368618 | 0.220068 | downstream-variant-500B | CHFR | GRCh38.p7 | 12:132839951 | CCCCTGCACTAACTC[C/G]GGACCTCCCTGCTCA | 55743 |
rs116585015 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | CHFR | GRCh38.p7 | 12:132853919 | GTGCTCCTCAGGACC[C/T]GCCTACTCTCCCGTT | 55743 |
rs116613429 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | CHFR | GRCh38.p7 | 12:132873358 | CACAGCCGTCTCCCC[A/G]TAAAACCTCCGAAAC | 55743 |
rs116913585 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | CHFR | GRCh38.p7 | 12:132863453 | GGAGTTGCAGCGAAC[A/G]AAGTTCGCGCCATTG | 55743 |
rs116939478 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | CHFR | GRCh38.p7 | 12:132843600 | CCTGTATGGCCTGAC[A/G]TCCTGCCGGCTCCTG | 55743 |
rs117183760 | snp | A/G | | | downstream-variant-500B | CHFR | GRCh38.p7 | 12:132839990 | CCTGCACTAACTCAG[A/G]ACCTCCCTGCTCAGC | 55743 |
rs117246365 | snp | C/T | 0.0142736 | 0.0832652 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132840711 | CCCTGGGCTTGGGGC[C/T]GTGGTCACTCACACA | 55743 |
rs117295646 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132866673 | TGTTACAACACACCA[C/G]AATGTTACAGGAATG | 55743 |
rs117363206 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132853358 | GCAGAGCGCGGCCAC[A/G]TGCACGTCAGCACCG | 55743 |
rs117389842 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | CHFR | GRCh38.p7 | 12:132860288 | GACACCCCTGCCAAC[A/G]TTACATTAACAGATT | 55743 |
rs117485838 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | CHFR | GRCh38.p7 | 12:132874857 | CCCAGTGCAGGGAAC[C/G]CAGGCCCTGGAACAG | 55743 |
rs117630891 | snp | A/G | 0.0501905 | 0.150254 | downstream-variant-500B | CHFR | GRCh38.p7 | 12:132840132 | CTTCTTCTGGTGCTC[A/G]GCTGAAGACAAAGCC | 55743 |
rs117696161 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CHFR | GRCh38.p7 | 12:132853706 | TGAGGGGAAGGGCCG[A/G]GCCCCATTCCTGTCC | 55743 |
rs117783146 | snp | A/G | | | downstream-variant-500B | CHFR | GRCh38.p7 | 12:132839988 | CCCCTGCACTAACTC[A/G]GAACCTCCCTGCTCA | 55743 |
rs117802940 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | CHFR | GRCh38.p7 | 12:132884929 | CCATCTCTACTAAAA[C/T]AGAAAAAAATAAGCC | 55743 |
rs117877326 | snp | C/G | 0.0501905 | 0.150254 | intron-variant | CHFR | GRCh38.p7 | 12:132880246 | AAAACTATGAAACTT[C/G]CAGTGGAAAAGACAG | 55743 |
rs117926102 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132882806 | GAACTCCCAGGCTCA[A/C/T]GTGATCCTCCCACTT | 55743 |
rs118158105 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | CHFR | GRCh38.p7 | 12:132866237 | TAGCACCTGAGAAGT[C/T]CTCCCAGGTGAGTCC | 55743 |
rs137860747 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132840838 | CCCAGGCTCGGGGCC[A/G]CGGTCACTCACCGGT | 55743 |
rs137935176 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | CHFR | GRCh38.p7 | 12:132871935 | GGTCTCCAAAAGCAG[A/G]ACCATCAATGGCCTC | 55743 |
rs137976420 | snp | A/T | 0.0275645 | 0.114116 | intron-variant | CHFR | GRCh38.p7 | 12:132851908 | CACCCAAACTCGGGG[A/T]GTCAAAACAGATTAA | 55743 |
rs138207644 | snp | A/G | 0.000157899 | 0.00888395 | missense | CHFR | GRCh38.p7 | 12:132853460 | ACGGACGTGGAGGGT[A/G]CATCCCCCAGGGCCT | 55743 |
rs138280939 | snp | A/G | 6.76053e-05 | 0.00581361 | synonymous-codon | CHFR | GRCh38.p7 | 12:132857532 | CGAGTAGCAAGCCGC[A/G]CAGAACGTGTGCATG | 55743 |
rs138313072 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132860100 | GGCAGTCACCCTCCG[A/T]CTCAGCCGCTCCTCA | 55743 |
rs138320999 | snp | C/T | 0.000642467 | 0.0179115 | synonymous-codon | CHFR | GRCh38.p7 | 12:132872382 | CAGCTTGTTAATCAC[C/T]GTTCCACTGGTGCTG | 55743 |
rs138326778 | snp | A/C/G | 4.99139e-05 | 0.00499544 | intron-variant | CHFR | GRCh38.p7 | 12:132856735 | GCTGCGGAAGGAGGG[A/C/G]TCTGGGCGGACCGCC | 55743 |
rs138360531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132847369 | ACCAGAGTCTCTCAA[A/G]AGTTCTGCCAAGACC | 55743 |
rs138363744 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | CHFR | GRCh38.p7 | 12:132870081 | AGGCGTGCCGGGCGC[A/G]GTGGCTCATACCTGT | 55743 |
rs138447671 | snp | A/G | 0.235854 | 0.249599 | intron-variant | CHFR | GRCh38.p7 | 12:132878616 | CAAGGTCAGGAGATC[A/G]AGACCATCCTGGCTA | 55743 |
rs138637226 | snp | C/T | 6.64496e-05 | 0.00576371 | missense | CHFR | GRCh38.p7 | 12:132861617 | TTCCTTTAGGGGAGA[C/T]GCCACCACCCCCAGA | 55743 |
rs138774984 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132871630 | TACAAAAATGAGCCG[G/T]GCGTGGTGGTGGGCA | 55743 |
rs138793246 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | CHFR | GRCh38.p7 | 12:132867280 | CACTGAGTCCCTGCA[A/C]CCGATGCCGCTCCTT | 55743 |
rs138832251 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | CHFR | GRCh38.p7 | 12:132864866 | ATTATCAAAAAATTA[C/T]GCAAACCGTATTACC | 55743 |
rs138833456 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132863610 | CCAACGGGTGGAGAT[A/G]GTGCTGCGTGTGAAC | 55743 |
rs138943152 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | CHFR | GRCh38.p7 | 12:132881025 | TAATCCCATCACTTT[G/T]GGTGGCCAAGGCGGG | 55743 |
rs139032849 | snp | G/T | 0.00075918 | 0.0194683 | intron-variant | CHFR | GRCh38.p7 | 12:132859251 | GAAAGGGATGTGTTC[G/T]GTCGTAACCAAGAAG | 55743 |
rs139045656 | snp | C/T | 0.00226693 | 0.0335906 | intron-variant, missense | CHFR | GRCh38.p7 | 12:132862408 | GACCAGCCTGGGCAA[C/T]ACAGCAAGGCACCAT | 55743 |
rs139147691 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CHFR | GRCh38.p7 | 12:132857864 | GCGGAAAAGCAAGGA[A/G]GCCCTTCCTCAGCGG | 55743 |
rs139235273 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | CHFR | GRCh38.p7 | 12:132849832 | TGACCTCAGGTCATC[C/T]GCCTGCCTTGGCCTC | 55743 |
rs139274813 | in-del | -/AC | 0.0103295 | 0.0711199 | intron-variant | CHFR | GRCh38.p7 | 12:132843250 | ATTTCAGGAAAGGAA[-/AC]ACATGTTTAACTAAA | 55743 |
rs139281535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132879879 | GCAAACATACTTTTC[C/T]TAAACGTTCCACACA | 55743 |
rs139341825 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CHFR | GRCh38.p7 | 12:132845707 | ACTCCACAAAGCATC[A/G]TGTGCCCCCCTGGAG | 55743 |
rs139343436 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CHFR | GRCh38.p7 | 12:132849515 | AAATCTCACCTGCTC[C/T]ACCACCCTAACACGG | 55743 |
rs139569750 | in-del | -/AATA | | | intron-variant | CHFR | GRCh38.p7 | 12:132885427 | AAAATATATAAATAA[-/AATA]ATAAATAAATAAATA | 55743 |
rs139572963 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CHFR | GRCh38.p7 | 12:132882593 | GTCAAGCTCTTCCCA[C/T]TCCATTGAGCGTTAA | 55743 |
rs139666428 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CHFR | GRCh38.p7 | 12:132868351 | AAAAATTAGCCAGGC[A/G]TGGTGACGGGTGCCT | 55743 |
rs139830167 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132845078 | CAATTTAAACATCAA[A/C]ATTAAAATAAATACA | 55743 |
rs139851613 | snp | G/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132872627 | CTACACCTCCTCACG[G/T]GCTTGGCAGCTCTGC | 55743 |
rs139904993 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | CHFR | GRCh38.p7 | 12:132853762 | AGAACGAGTCGAAGG[A/G]CAAGGACACGCCACT | 55743 |
rs140026593 | snp | C/T | 0.0041221 | 0.0452113 | intron-variant | CHFR | GRCh38.p7 | 12:132853619 | CAGGCCCCAAGCCTC[C/T]CAGGTAGGGCCGGTG | 55743 |
rs140029976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132868434 | AATGGCGTGGGAGGC[A/G]GAGCTTGCAGTGAGC | 55743 |
rs140117476 | in-del | -/A | 0.246769 | 0.249979 | upstream-variant-2KB | CHFR | GRCh38.p7 | 12:132889284 | CTGTCAAAAAAAAAA[-/A]TAACAAAATAGAAAC | 55743 |
rs140233697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132873104 | CGACACACAAAACGG[C/T]AACCGGGCAAAACGA | 55743 |
rs140306643 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132887001 | AACTTATACAGTTGT[A/C]ACGAAGGCTAAATGA | 55743 |
rs140355424 | snp | A/G | 0.207253 | 0.246318 | intron-variant | CHFR | GRCh38.p7 | 12:132844458 | CCGGGCTAATTTTTT[A/G]TATTTTTAGTAGAGA | 55743 |
rs140443838 | snp | G/T | 0.244776 | 0.249945 | intron-variant | CHFR | GRCh38.p7 | 12:132844454 | CACACCGGGCTAATT[G/T]TTTGTATTTTTAGTA | 55743 |
rs140668278 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132865607 | CAAGCTCCTGACCTC[A/C]AGTGATTCGCCTGTC | 55743 |
rs140742448 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | CHFR | GRCh38.p7 | 12:132862958 | CTGGAGTGCAGTGGC[A/G]TGATCTTGGCTCACT | 55743 |
rs140818151 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CHFR | GRCh38.p7 | 12:132874220 | CCATTAAGCTTGTGG[C/T]AAATTACAATAGCCA | 55743 |
rs140943466 | snp | A/G | 0.319856 | 0.240042 | intron-variant | CHFR | GRCh38.p7 | 12:132863188 | GGCGTGAGCCACCGC[A/G]CCCGGCCTGACCTCA | 55743 |
rs141021277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132851419 | GATGGAGATGTAGCC[C/T]GTGAAGGGGCAATGT | 55743 |
rs141044759 | in-del | -/AGT | 0.0501905 | 0.150254 | intron-variant | CHFR | GRCh38.p7 | 12:132860366 | TTCACTGCTGAGCCA[-/AGT]AGTTTACTAGATTAA | 55743 |
rs141053335 | snp | C/T | 0.000298972 | 0.0122228 | intron-variant | CHFR | GRCh38.p7 | 12:132859059 | AGCCAAGGGTGAACA[C/T]GGTCGCACCTCACGC | 55743 |
rs141163483 | snp | A/C/G/T | 0.000496331 | 0.0157468 | intron-variant | CHFR | GRCh38.p7 | 12:132846993 | GACACGCAGGCACAG[A/C/G/T]CCTGGACACTCACAT | 55743 |
rs141179419 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | CHFR | GRCh38.p7 | 12:132845614 | GTGATCATGCCCCTG[C/T]ACTCCAGCCTGGGCG | 55743 |
rs141183005 | snp | A/G | 0.000263544 | 0.0114762 | missense | CHFR | GRCh38.p7 | 12:132861523 | TCCTGGGGTTCCAAC[A/G]ACGAAAAGGACGCAG | 55743 |
rs141275031 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132885861 | CTTCACCAAACCTCC[A/C/T]AGTCTATCAAGTAAA | 55743 |
rs141279129 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132858837 | TAGTCCCAGCAACTC[A/T]GAAGGCTGAGGTCAG | 55743 |
rs141315477 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | CHFR | GRCh38.p7 | 12:132868988 | GGGAAGGGGACATGC[A/G]GAGTGACTGCTGCTG | 55743 |
rs141349945 | snp | A/G | 4.99821e-05 | 0.00499885 | synonymous-codon | CHFR | GRCh38.p7 | 12:132851724 | TTGCAGAGGGCACAC[A/G]TAATCCTGGACTGCT | 55743 |
rs141404869 | snp | C/G | 4.95193e-05 | 0.00497566 | missense | CHFR | GRCh38.p7 | 12:132857458 | AGGATGTGGTTTTTA[C/G]AGATCCGCTCCACGG | 55743 |
rs141410401 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | CHFR | GRCh38.p7 | 12:132879370 | GCTGAATACAGTAAT[C/T]CTGACACTTTGGGAT | 55743 |
rs141515753 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | CHFR | GRCh38.p7 | 12:132875906 | CTGGCCGGGCGCGAT[G/T]GCTCACGCCTGTAAT | 55743 |
rs141555038 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | CHFR | GRCh38.p7 | 12:132870099 | GGCTCATACCTGTAA[G/T]CCCAGCACTTTGGGA | 55743 |
rs141613946 | in-del | -/A | 0.495891 | 0.0451408 | intron-variant | CHFR | GRCh38.p7 | 12:132884415 | TCTCAAAAAAAAAAA[-/A]TACATATATATATAT | 55743 |
rs141728111 | in-del | -/T | 0.00438332 | 0.0466095 | intron-variant | CHFR | GRCh38.p7 | 12:132850234 | AATTATTTTTAATTG[-/T]CTGATATTCTATACA | 55743 |
rs141735852 | in-del | -/ATAA | | | intron-variant | CHFR | GRCh38.p7 | 12:132885420 | TGTCTCAAAAAATAT[-/ATAA]ATAAATAAATAAATA | 55743 |
rs141763844 | snp | C/G | 0.00302541 | 0.0387756 | missense, intron-variant | CHFR | GRCh38.p7 | 12:132869827 | GAACACATTTTCCTT[C/G]TTAGCTTCTGTAACC | 55743 |
rs141835819 | snp | C/T | 0.00130969 | 0.0255564 | missense | CHFR | GRCh38.p7 | 12:132853446 | CTGTCGTCAGGCTGA[C/T]GGACGTGGAGGGTGC | 55743 |
rs141942403 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | CHFR | GRCh38.p7 | 12:132859541 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCGTGTT | 55743 |
rs141967795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132855491 | CCAATGTGGTAAAAC[C/T]CCATCTCTACTAAAA | 55743 |
rs142112731 | snp | A/G | 0.0700422 | 0.173537 | intron-variant | CHFR | GRCh38.p7 | 12:132852268 | GCTGGGATTACAGGC[A/G]TGAGCCACCGTGCCC | 55743 |
rs142165233 | snp | A/G/T | 0.000143465 | 0.0084684 | intron-variant | CHFR | GRCh38.p7 | 12:132877657 | GAAAGGTCGCAACCT[A/G/T]AAAAAGAGAGGGTGG | 55743 |
rs142337474 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | CHFR | GRCh38.p7 | 12:132844957 | TATAAAATTTAAATA[C/T]TAAAACTCCCAAAAA | 55743 |
rs142376269 | snp | A/C | 0.0023933 | 0.0345097 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132841118 | AGCAGGATATTGTGT[A/C]CGTCCTGTAGGCTGT | 55743 |
rs142414536 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CHFR | GRCh38.p7 | 12:132872217 | TGTAGCCAGGAGGAA[C/T]GTTCAGAGAGCGCCC | 55743 |
rs142480647 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CHFR | GRCh38.p7 | 12:132871288 | GAAACCCTGTCTGTA[C/T]TAAAAATACAAAAAT | 55743 |
rs142511371 | snp | C/T | 0.000153386 | 0.00875611 | synonymous-codon | CHFR | GRCh38.p7 | 12:132851637 | CTGAGGGGCGACACG[C/T]GGGTCCTGCTCGCGC | 55743 |
rs142526117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132865416 | CTGGAGTGCAGTGAC[A/G]CGGTATCGGCTCACT | 55743 |
rs142721238 | in-del | -/A | | | intron-variant | CHFR | GRCh38.p7 | 12:132874201 | AAATTTGTGTTTTTT[-/A]AATCCATTAAGCTTG | 55743 |
rs142792187 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CHFR | GRCh38.p7 | 12:132881596 | CCACGGGCCGGGCAC[A/G]GTGGCTCACGCCTGT | 55743 |
rs142807294 | in-del | -/ATTG | 0.00676609 | 0.0577691 | intron-variant | CHFR | GRCh38.p7 | 12:132856312 | CTAATACTATCCAAT[-/ATTG]ATCAGAAAACAAGCT | 55743 |
rs142824452 | snp | A/G | 4.99305e-05 | 0.00499628 | missense | CHFR | GRCh38.p7 | 12:132877597 | GATTTTTCATCCACT[A/G]CAATTCTACAGTGAT | 55743 |
rs142851103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132864900 | ACTACACACTGTGCT[A/G]TGCACATTGGTGGAT | 55743 |
rs142944026 | snp | C/T | 0.00398564 | 0.0444627 | upstream-variant-2KB, nc-transcript-variant | CHFR, LOC101928530 | GRCh38.p7 | 12:132888491 | ATATACACACATATA[C/T]ACATATATAAACATT | 55743 |
rs142955557 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | CHFR | GRCh38.p7 | 12:132843409 | TCAGCCTGGGCGACA[A/G]AGTCAGACTCTGTCT | 55743 |
rs142975525 | snp | C/T | 3.41682e-05 | 0.00413315 | synonymous-codon | CHFR | GRCh38.p7 | 12:132857538 | GCAAGCCGCGCAGAA[C/T]GTGTGCATGCAGGGC | 55743 |
rs143067060 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | CHFR | GRCh38.p7 | 12:132875033 | AGGCCCTGATGTAGG[A/C]AGGAAAGCCCAGGAC | 55743 |
rs143077874 | snp | G/T | 0.244205 | 0.249933 | intron-variant | CHFR | GRCh38.p7 | 12:132844475 | ATTTTTAGTAGAGAC[G/T]GGGTTTCACCGTGTT | 55743 |
rs143181439 | snp | A/G | 1.65217e-05 | 0.00287412 | synonymous-codon | CHFR | GRCh38.p7 | 12:132857418 | GCCTGGATGCTGGAT[A/G]AGGTATGCTTCCACG | 55743 |
rs143228809 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132853017 | TCGCATTAAGCCAAC[C/T]CTGGTGACGCAGGGC | 55743 |
rs143229713 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | CHFR | GRCh38.p7 | 12:132868220 | GTCACGGCTGGGCGC[A/G]GCAGCTCACGCCTGT | 55743 |
rs143267510 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | CHFR | GRCh38.p7 | 12:132849651 | CCTAGGCTGGAGTAT[A/C]GTGGAGCAATCTCGG | 55743 |
rs143327405 | in-del | -/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132856239 | ACGCTCTGCTGGCTA[-/C]CCCCTGGCTACCCCG | 55743 |
rs143399245 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | CHFR | GRCh38.p7 | 12:132856877 | GCTGGTGTGTGGATG[C/T]CCTCACTTGCCTGGG | 55743 |
rs143410797 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CHFR | GRCh38.p7 | 12:132853945 | CCGTTAAAAGCAGAG[C/T]GCGGTGGGCAACGTA | 55743 |
rs143440255 | in-del | -/CCAGCAACA | 0.319419 | 0.240169 | intron-variant | CHFR | GRCh38.p7 | 12:132844158 | AACACAGCCAGTTAC[-/CCAGCAACA]CCATCTTCCCAACAG | 55743 |
rs143449794 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132851476 | ATTCAATATGGTGAC[A/G]TGGGGAAAACTGATC | 55743 |
rs143484509 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132848924 | GGAGTTGTATCCCTG[A/C]AAAAAGGCGAGGCTC | 55743 |
rs143499905 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CHFR | GRCh38.p7 | 12:132858926 | CCACCCACTCCACCC[A/G]CTTATCTGGGTGACA | 55743 |
rs143653967 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132853672 | CAGCTCAGCTCCACC[A/G]TCGCTCAGCTGCTTG | 55743 |
rs143791143 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | CHFR | GRCh38.p7 | 12:132865498 | CTGTCTCAGCTTCCT[A/G]AGTAGCTGGGACTAC | 55743 |
rs143802556 | in-del | -/ATA | 0.24449 | 0.249939 | intron-variant | CHFR | GRCh38.p7 | 12:132850267 | GGAAATCCCTAAAAT[-/ATA]ATGTTAGGTAAACCC | 55743 |
rs143823887 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132881466 | TCAAAGAAGAGATAT[A/G]GATGGCAAATTAAGC | 55743 |
rs143909745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132867797 | AGCCGTGAGACTTCA[C/T]TGAAGAACAGGAAGA | 55743 |
rs143973086 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | CHFR | GRCh38.p7 | 12:132849228 | CGCTAGGATTACAGG[A/C]ATGATGCACTGCGCC | 55743 |
rs144056023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132876605 | GAAATCAAACTTGAA[C/T]AGGCTTGCAAGAACC | 55743 |
rs144096020 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | CHFR | GRCh38.p7 | 12:132850496 | CACCTGCCCTCCCAC[A/G]TGCAGCATCAGCAGT | 55743 |
rs144115179 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132880069 | CACTGACAAGCTGAT[G/T]CTAAAGTTCACAGAA | 55743 |
rs144198914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132861745 | GCAGCCTGAGATGTC[A/G]TAGTTTAGGAATGAC | 55743 |
rs144230604 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CHFR | GRCh38.p7 | 12:132858643 | TGAGGTAGGAGAATC[A/G]TCTGAACCCGGGAGG | 55743 |
rs144278060 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CHFR | GRCh38.p7 | 12:132850046 | GCAACCTCTGCCTCC[C/T]GGGTTCACGCCATTC | 55743 |
rs144290290 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CHFR | GRCh38.p7 | 12:132860981 | TGGTCTTGAACTCCT[A/G]ACCTCAGATGATCCG | 55743 |
rs144432167 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132868367 | TGGTGACGGGTGCCT[A/G]TAGTCCCAGCTACTC | 55743 |
rs144469046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132865747 | ACATTGTAACCTCTG[C/T]CTCCCAGGCTCAGGC | 55743 |
rs144627058 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | CHFR | GRCh38.p7 | 12:132845252 | CAAGGTCAGGAGTTC[A/G]AGACCAGCCTAACCA | 55743 |
rs144644143 | snp | C/T | 1.65586e-05 | 0.00287733 | missense | CHFR | GRCh38.p7 | 12:132844056 | GCAGGAATGTTCTGC[C/T]GATACTGATAGGTCA | 55743 |
rs144740160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132885750 | CCTCAGAGCAAATCT[A/G]TGAAGTAGGTACATA | 55743 |
rs144757764 | in-del | -/CTC | 0.0528381 | 0.153711 | intron-variant | CHFR | GRCh38.p7 | 12:132854249 | TGAGATTACCTACTT[-/CTC]CTTCTAAACTGGCAA | 55743 |
rs144812156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132842620 | CGGGAAAGACACCAC[A/G]TGAGGGTGACGATGT | 55743 |
rs144824959 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132853020 | CATTAAGCCAACTCT[G/T]GTGACGCAGGGCAGC | 55743 |
rs144830406 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132872826 | TGATCCCTCCCAAGA[C/G]ACTGGCTCTGGGCAG | 55743 |
rs144838296 | snp | C/T | 8.23906e-05 | 0.00641783 | missense | CHFR | GRCh38.p7 | 12:132859159 | CTGCTCTGACGTCCT[C/T]GTGGACGGTTTGGGC | 55743 |
rs144888932 | snp | A/C/G | 6.71709e-05 | 0.00579496 | intron-variant | CHFR | GRCh38.p7 | 12:132847167 | GAATAAGAAATACTC[A/C/G]TTTAGAGGAAGAAAC | 55743 |
rs144980907 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | CHFR | GRCh38.p7 | 12:132871415 | TGAGATCACGCCATT[C/G]CACTCCAGCCTCCGC | 55743 |
rs145025916 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | CHFR | GRCh38.p7 | 12:132883738 | AACAAGGTTGTTGCA[C/G]CCCTTCCTACACGTT | 55743 |
rs145065421 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132883066 | TATTCACAGCATTTG[C/T]TGCGCTTGACGCTTG | 55743 |
rs145166244 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CHFR | GRCh38.p7 | 12:132889415 | AAATCTTTGAATCCA[C/T]CTATGAACTTTCTCC | 55743 |
rs145246258 | snp | A/C/T | 0.000592885 | 0.0172077 | synonymous-codon | CHFR | GRCh38.p7 | 12:132861525 | CTGGGGTTCCAACGA[A/C/T]GAAAAGGACGCAGTC | 55743 |
rs145288754 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | CHFR | GRCh38.p7 | 12:132871860 | CACAAAACAAAAACG[C/G]GACTTCTGGAGCTGA | 55743 |
rs145418785 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | CHFR | GRCh38.p7 | 12:132866253 | CTCCCAGGTGAGTCC[C/G]GAAATCACATCAGAA | 55743 |
rs145476163 | snp | C/T | 0.199564 | 0.24486 | intron-variant | CHFR | GRCh38.p7 | 12:132844474 | TATTTTTAGTAGAGA[C/T]TGGGTTTCACCGTGT | 55743 |
rs145490779 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | CHFR | GRCh38.p7 | 12:132846618 | GGGCATAGTGGCTCA[C/T]GCCTGTAATTCCAGC | 55743 |
rs145527630 | snp | C/T | 0.0983112 | 0.198722 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132887189 | GGCCCCGGCCTCAGC[C/T]CCGCACCTCGTCTCC | 55743 |
rs145559451 | in-del | -/ATATATATATATAT | | | intron-variant | CHFR | GRCh38.p7 | 12:132850965 | ACTGTATGTGTGTGC[-/ATATATATATATAT]ATATATATATATATA | 55743 |
rs145603023 | in-del | -/AG | 0.367091 | 0.220884 | intron-variant | CHFR | GRCh38.p7 | 12:132880664 | CTCCGACTCAAAAAA[-/AG]AAAAAAAAAGTCAAT | 55743 |
rs145622325 | snp | C/T | 0.000263548 | 0.0114763 | missense | CHFR | GRCh38.p7 | 12:132872350 | TGTAAAGGGCATGTC[C/T]GCTTCTTAACAACCT | 55743 |
rs145650461 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CHFR | GRCh38.p7 | 12:132882660 | GCAAGTCACGGTGTC[A/G]CCAGAGCCAGTTTGT | 55743 |
rs145658744 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132859938 | TGGTCTCAGCTACTC[A/G]GAAGGCTGAGGTGGG | 55743 |
rs145962987 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | CHFR | GRCh38.p7 | 12:132842095 | GCCTGGCAGACAGAG[C/T]GAGACTCCATCTCAA | 55743 |
rs146060398 | in-del | -/GA | | | intron-variant | CHFR | GRCh38.p7 | 12:132880665 | TCCGACTCAAAAAAA[-/GA]AAAAAAAAGTCAATT | 55743 |
rs146088609 | snp | A/T | 5.07816e-05 | 0.00503867 | missense | CHFR | GRCh38.p7 | 12:132877634 | AGACCAGTTTATTGC[A/T]GGGGAAGGAAAGGTC | 55743 |
rs146098239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132879757 | CAAAAGAACAAAGGC[A/G]TTTTAATATCTCATC | 55743 |
rs146107503 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon | CHFR | GRCh38.p7 | 12:132859094 | GTGCAGCAGGTCCTG[A/G]CAGATGATGCATGTC | 55743 |
rs146156998 | snp | C/T | 0.000102135 | 0.00714541 | missense | CHFR | GRCh38.p7 | 12:132848676 | CCGTAGCAGCCGGTC[C/T]GGGTGCAGCCCCAGT | 55743 |
rs146218621 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | CHFR | GRCh38.p7 | 12:132868306 | CCATCCTGGCTAACA[C/T]GGTGAAACTCCGTCT | 55743 |
rs146332668 | snp | A/G | 0.000175929 | 0.00937728 | synonymous-codon | CHFR | GRCh38.p7 | 12:132843016 | CTGCACTCACATGGC[A/G]TGGTGAGCTTTCACC | 55743 |
rs146337818 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132853751 | AGAGAGGGACCAGAA[C/T]GAGTCGAAGGGCAAG | 55743 |
rs146343801 | snp | C/T | 1.65222e-05 | 0.00287417 | missense | CHFR | GRCh38.p7 | 12:132857479 | CGCTCCACGGGACAG[C/T]GGCAGGTAGGACACA | 55743 |
rs146400366 | in-del | -/GGTGACTT | 0.243633 | 0.249919 | intron-variant | CHFR | GRCh38.p7 | 12:132845781 | CACCAAGTCCCCGAG[-/GGTGACTT]GGTCCCAGGACAACT | 55743 |
rs146473032 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CHFR | GRCh38.p7 | 12:132850769 | AACACCGGTGTGTGC[A/G]GCAGGAGCCAACCGC | 55743 |
rs146514119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132880107 | GTAGAAAAACCAAAG[C/T]AATTTTGAAAAAGAA | 55743 |
rs146529068 | in-del | -/TT | | | downstream-variant-500B | CHFR | GRCh38.p7 | 12:132839925 | ACTTGGGACCTCCCC[-/TT]CCTTAGCCTCGCCCC | 55743 |
rs146711897 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CHFR | GRCh38.p7 | 12:132877804 | GAAAGACATAAAGAA[A/G]TTTTTTTTTTTTTCT | 55743 |
rs146832553 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | CHFR | GRCh38.p7 | 12:132865518 | GCTGGGACTACAGGC[A/G]CCTGCCACCATGCCT | 55743 |
rs146856316 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | CHFR | GRCh38.p7 | 12:132880992 | AAAAGTAAGGCTGGG[C/G]GCGGTGGTTCACGCC | 55743 |
rs146862603 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | CHFR | GRCh38.p7 | 12:132871379 | ATCGCTTGAAACCAG[G/T]AGGTGGAGGTTGCAG | 55743 |
rs146941862 | in-del | -/A | | | intron-variant | CHFR | GRCh38.p7 | 12:132854065 | GTCAACTGTAAAAAA[-/A]GAACCTGTAGGAAAA | 55743 |
rs146950693 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | CHFR | GRCh38.p7 | 12:132880834 | GCCAGGCATGGTGGC[A/G]GGCGCCTATAATCCC | 55743 |
rs146976267 | snp | A/G | 0.00519434 | 0.050697 | synonymous-codon | CHFR | GRCh38.p7 | 12:132851733 | GCACACGTAATCCTG[A/G]ACTGCTGAAGCACAC | 55743 |
rs146982142 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132853147 | CATCAGCTGCCCTGA[A/G]GCAGTGGCTGGGGAG | 55743 |
rs147128291 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886965 | ACAATATTGCATTCT[A/G]GAGAGTATATGAACA | 55743 |
rs147204982 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132864329 | TCATCTCCAGCGCCC[C/T]GTGCTCAGCCAACGT | 55743 |
rs147213046 | snp | A/G | 1.67719e-05 | 0.0028958 | intron-variant | CHFR | GRCh38.p7 | 12:132861436 | CAGGAGCACACGAGA[A/G]GACTGAGGACACACA | 55743 |
rs147320591 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CHFR | GRCh38.p7 | 12:132879138 | GCCTCCTGAGCAGCT[A/G]GGACTACAGGCATGC | 55743 |
rs147425936 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132867534 | CTGTGAAACCTCGAG[C/G]CAAAAACCTGAGCAA | 55743 |
rs147435711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132865183 | TCTATTCCTCTGGGG[C/T]TGTCCCTGCACGGGG | 55743 |
rs147521868 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132876367 | GAAATCCAAAACTTT[C/T]TGAGCACCAACAAGA | 55743 |
rs147538398 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CHFR | GRCh38.p7 | 12:132849792 | ATGGGGTCTCACCGC[A/G]TTGGTCAGGCTGGTC | 55743 |
rs147588269 | in-del | -/AAAC | | | intron-variant | CHFR | GRCh38.p7 | 12:132868502 | CGAGACTCCATCTCA[-/AAAC]AAACAAACAAACAAA | 55743 |
rs147596604 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | CHFR | GRCh38.p7 | 12:132880892 | ATGGTGGGAACCCAG[G/T]AAGCGGAGGTTACAG | 55743 |
rs147700426 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | CHFR | GRCh38.p7 | 12:132868663 | CCAGCCTGAGCGACA[C/G]AGCGAGACTCCGTCT | 55743 |
rs147735159 | in-del | -/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132855524 | CAAAAAAATTAGCTG[-/G]GGTGTGGTGGCATGC | 55743 |
rs147750032 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132843733 | GCACTTTGGGAGGCC[A/G]AGGTCAAGAGTTCGA | 55743 |
rs147759415 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CHFR | GRCh38.p7 | 12:132861995 | ACAGAGCTTTGGGCC[A/G]GGTGCGGTGGCTCAC | 55743 |
rs147791929 | snp | A/G | 0.00133072 | 0.0257602 | synonymous-codon | CHFR | GRCh38.p7 | 12:132851700 | GCAGGTGCACAGGGC[A/G]TGGCTTCCTTGCAGA | 55743 |
rs147795442 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | CHFR | GRCh38.p7 | 12:132858718 | GGTGACAGAGCGAGA[C/T]TCCATCTAAAAAAAA | 55743 |
rs147803503 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | CHFR | GRCh38.p7 | 12:132855622 | CAGTGAGCTGAGATC[A/G]TGTCACTGCACTCCA | 55743 |
rs147803776 | snp | C/G | 0.000153988 | 0.00877328 | missense | CHFR | GRCh38.p7 | 12:132861509 | CCAAATCCTCCTGAT[C/G]CTGGGGTTCCAACGA | 55743 |
rs147898853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132844190 | CCAACAGCAGCGCAC[A/G]GACTTCACAGCAGTG | 55743 |
rs148014487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132849032 | GCTCACTGCAACCTC[C/T]GCCTCCTGGGTTCAA | 55743 |
rs148058789 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132869516 | CTACTGAGAACCTCA[G/T]GCCAGTCCTCAGTCG | 55743 |
rs148079332 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132881522 | AATCTTCAGAGAAAT[G/T]CAAATTAAAACCATG | 55743 |
rs148176220 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132853323 | GCCCAAAGGGGGCGA[A/G]CAGTGCAGACAGGAG | 55743 |
rs148228769 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | CHFR | GRCh38.p7 | 12:132875305 | ACAGCACACTCTCAA[A/C]ATACTGCTAGAAGAC | 55743 |
rs148239859 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132885778 | ATAGGCGCAGAAAGA[C/T]GTCGTTAGCCCAGAG | 55743 |
rs148270257 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132840430 | GATTGCTGCTTCTCA[A/G]TTTCTATCAAGAGCA | 55743 |
rs148311652 | snp | A/G | 0.000181676 | 0.00952915 | synonymous-codon | CHFR | GRCh38.p7 | 12:132857421 | TGGATGCTGGATGAG[A/G]TATGCTTCCACGAGG | 55743 |
rs148446051 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132861104 | GCCCAGGCTGGTCTC[C/G]AACGCCTGACCTCAA | 55743 |
rs148544894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132877475 | TTCTCCTCCTCAGCC[A/G]TGGCACACAGCACAG | 55743 |
rs148561248 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132842756 | AACGGCTAAGCCTGA[A/T]ATGATGGGGTGTGCC | 55743 |
rs148613276 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CHFR | GRCh38.p7 | 12:132868118 | GGTAAGAGTCATGCC[A/G]TAAGGAACAGCATCT | 55743 |
rs148618944 | snp | C/T | 0.0004291 | 0.0146412 | missense | CHFR | GRCh38.p7 | 12:132859192 | TTCTACGCGGTTGTG[C/T]GACCAACAACTGCCC | 55743 |
rs148658321 | in-del | -/A | | | intron-variant | CHFR | GRCh38.p7 | 12:132882435 | GTGAGTACATTTCCC[-/A]AAACTCATGGAACTG | 55743 |
rs148702719 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CHFR | GRCh38.p7 | 12:132880279 | AAAAATCTTAGTGCC[A/G]TTGGGTCTTGCATGG | 55743 |
rs148912880 | snp | C/T | 0.046775 | 0.145601 | intron-variant | CHFR | GRCh38.p7 | 12:132854812 | CTCCATCTCAAAAAA[C/T]AAACAAACAAAAAAT | 55743 |
rs148932455 | snp | C/T | 6.83037e-05 | 0.00584356 | splice-acceptor-variant | CHFR | GRCh38.p7 | 12:132861636 | ACCACCCCCAGACCC[C/T]GTGAGAGGAATCAAA | 55743 |
rs148977023 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | CHFR, LOC101928530 | GRCh38.p7 | 12:132887868 | AGCCCCAAGGATTCT[A/G]AGAGCCCCGCTAATC | 55743 |
rs149049647 | in-del | -/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132870552 | AAAAAAAAAAAAAAA[-/T]GGGAGACTGAAGCAG | 55743 |
rs149090452 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132871416 | GAGATCACGCCATTG[C/T]ACTCCAGCCTCCGCA | 55743 |
rs149132408 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132866317 | GAATGTTAACACACC[A/G]GAATGTTACAACACA | 55743 |
rs149249950 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132848576 | CCCCACCATCCCCTG[C/T]CCTCAAGTTCACCAA | 55743 |
rs149411171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132872803 | GAACTCATGCCTCCA[A/G]TGAGTACTGATCCCT | 55743 |
rs149423120 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CHFR | GRCh38.p7 | 12:132855518 | AAAAATACAAAAAAA[C/T]TAGCTGGGTGTGGTG | 55743 |
rs149454438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132867770 | AAGAATGAGCCCAGA[C/T]GACACGAAGAAAGCC | 55743 |
rs149505984 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CHFR | GRCh38.p7 | 12:132864244 | GTTTTGGGGACAAAC[C/T]ACCTCATATACGAAC | 55743 |
rs149619653 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | CHFR | GRCh38.p7 | 12:132845986 | CCCAATAAATATGAA[C/G]GGCTGTAGAAGCTCA | 55743 |
rs149628732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132856756 | GCGGACCGCCCTCAC[A/G]TGCCCGGGTGCTGGT | 55743 |
rs149683803 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132887020 | AAGGCTAAATGATGT[C/G]CGTGAATCATGCGCA | 55743 |
rs149728568 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132874547 | GGGGAAGCCAGGCCC[C/T]GGAACAGGCGGGACT | 55743 |
rs149735645 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | CHFR | GRCh38.p7 | 12:132882603 | TCCCATTCCATTGAG[C/G]GTTAACTGCCAGGAC | 55743 |
rs149820641 | in-del | -/A | 0.272511 | 0.248984 | intron-variant | CHFR | GRCh38.p7 | 12:132877769 | CCATTGTACATATGT[-/A]AAAAAAAACACTTGA | 55743 |
rs149862277 | snp | C/T | 0.00166314 | 0.0287889 | missense | CHFR | GRCh38.p7 | 12:132859149 | TTCCCAGCCGCTGCT[C/T]TGACGTCCTCGTGGA | 55743 |
rs149946482 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132857900 | ACGTTCATTCTATGC[A/G]AAATACACCTTCCCA | 55743 |
rs149990882 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132849833 | GACCTCAGGTCATCC[A/G]CCTGCCTTGGCCTCC | 55743 |
rs150035482 | in-del | -/AAAC | 0.311123 | 0.242413 | intron-variant | CHFR | GRCh38.p7 | 12:132870354 | CGACTCCATCTCAAA[-/AAAC]AAACAAACAAACAAA | 55743 |
rs150076004 | in-del | -/CATATATATA | | | intron-variant | CHFR | GRCh38.p7 | 12:132850964 | AACTGTATGTGTGTG[-/CATATATATA]TATATATATATATAT | 55743 |
rs150100592 | in-del | -/AG | 0.300926 | 0.244758 | intron-variant | CHFR | GRCh38.p7 | 12:132852007 | TTTTTTTTTTGAGAC[-/AG]AGTCTCACTCTGTCG | 55743 |
rs150170106 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132869873 | CAGCACACAACCAGG[A/G]CTCAAGCAGACACTC | 55743 |
rs150305533 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132851827 | GAAGCACAGCGAGGA[C/G]AGGTGCACCTGAGAC | 55743 |
rs150423813 | in-del | -/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132865653 | GCTGGGATTACAGGT[-/C]TTTTTTTTTTTTTTT | 55743 |
rs150467142 | snp | C/T | 1.64727e-05 | 0.00286986 | missense | CHFR | GRCh38.p7 | 12:132856568 | CTTTGGGCTGCAGCA[C/T]GTCTTGAGTGATTTT | 55743 |
rs150476934 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | CHFR | GRCh38.p7 | 12:132883595 | AGCCGGGCATGGTGG[C/T]GGGTGCCTGTAGTCC | 55743 |
rs150532689 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | CHFR | GRCh38.p7 | 12:132865418 | GGAGTGCAGTGACGC[C/G]GTATCGGCTCACTGC | 55743 |
rs150540137 | snp | A/G | 0.023684 | 0.106212 | intron-variant | CHFR | GRCh38.p7 | 12:132872237 | AGAGAGCGCCCTCAC[A/G]TGCACCCCCGTGCGG | 55743 |
rs150549422 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CHFR | GRCh38.p7 | 12:132882101 | ACTGCACACTTATGT[C/T]TATATTAGCTTTATT | 55743 |
rs150585952 | in-del | -/AAAAAAAAAAAAAAAC | | | intron-variant | CHFR | GRCh38.p7 | 12:132850910 | AGGAATACATTAAAA[-/AAAAAAAAAAAAAAAC]CAGCCATGAAATAAA | 55743 |
rs150627547 | snp | C/T | 0.0008317 | 0.0203754 | missense | CHFR | GRCh38.p7 | 12:132853560 | GACACTGCCGGCACA[C/T]GACGTATGGCTGGCT | 55743 |
rs150643970 | in-del | -/A | 0.408017 | 0.193729 | intron-variant | CHFR | GRCh38.p7 | 12:132843948 | CAGCGAAACTGTCTC[-/A]AAAAAAAAAAAGAGA | 55743 |
rs150742899 | in-del | -/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132884844 | GTAATCCTAGCACTT[-/T]GAGAGGCCGAGGCAG | 55743 |
rs150783439 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132857807 | CAGAGACAGCAAGTG[C/T]TTCTGGCCCAGAAGT | 55743 |
rs150837405 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | CHFR | GRCh38.p7 | 12:132879431 | AGTCTCTTTCTGTGG[C/T]CCAGGCTGGAGTGCA | 55743 |
rs150920425 | snp | C/T | 0.000118559 | 0.00769839 | missense | CHFR | GRCh38.p7 | 12:132851648 | CACGCGGGTCCTGCT[C/T]GCGCTCCGCTCTCCG | 55743 |
rs150995074 | snp | A/G | 8.23649e-05 | 0.00641683 | missense | CHFR | GRCh38.p7 | 12:132861535 | AACGACGAAAAGGAC[A/G]CAGTCTTTCTGTCTG | 55743 |
rs150996147 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132846160 | CAGCAGTAACTGCTG[C/T]AGTGAGGGTCTCAAG | 55743 |
rs151079292 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | CHFR | GRCh38.p7 | 12:132859012 | AGCCCTGCCCCACAC[A/G]GGACGAAGAACCTGC | 55743 |
rs151204644 | in-del | -/CATATATATATA | | | intron-variant | CHFR | GRCh38.p7 | 12:132850964 | AACTGTATGTGTGTG[-/CATATATATATA]TATATATATATATAT | 55743 |
rs151280652 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CHFR | GRCh38.p7 | 12:132873949 | GCTCACCACACGCTC[C/T]GACCACACAGCCCTG | 55743 |
rs151331438 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | CHFR | GRCh38.p7 | 12:132870652 | GTAACAGAGCGAGAC[C/T]CCATCTCAAAACACA | 55743 |
rs180679788 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132881739 | CGGGCATGGTGGCAC[C/G]TGCCTGTAGTCCCAG | 55743 |
rs180699073 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132867051 | AAAAACAGAAAATAA[A/G]GAGCACTCTGCTGCT | 55743 |
rs180700307 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CHFR | GRCh38.p7 | 12:132874531 | GACCAGCACCCAGCG[C/T]GGGGAAGCCAGGCCC | 55743 |
rs180708838 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CHFR | GRCh38.p7 | 12:132848317 | GAGGACAAGCAGAAA[C/T]GATTTCCATTCCACT | 55743 |
rs180709851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132855228 | GCCTGGGCAACAGAG[C/T]GAGACTTTGTCTCGA | 55743 |
rs180981527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132861324 | CTGAATGAAAATGCC[A/G]GAGGTGTTACAGGCA | 55743 |
rs181001509 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CHFR | GRCh38.p7 | 12:132878711 | TGTAATCCCAGCTAC[C/T]CAGGAGGATGAGGCA | 55743 |
rs181010161 | snp | C/G | 0.0174175 | 0.0916809 | upstream-variant-2KB, nc-transcript-variant | CHFR, LOC101928530 | GRCh38.p7 | 12:132888233 | AAAGACGGCGAGACG[C/G]GTCCACGCAGGGGGA | 55743 |
rs181013981 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | CHFR | GRCh38.p7 | 12:132871276 | GGCCAACACGGCGAA[A/C]CCCTGTCTGTACTAA | 55743 |
rs181025214 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132851513 | ATGGAAAAAAAGAAA[A/C/T]GGCATCCTTACTTCA | 55743 |
rs181323330 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132874903 | ACCAGCACCCAGCGC[A/G]GGGAAGCCAGGCCCT | 55743 |
rs181338231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132866047 | TGTTAAAACAAAGGT[A/G]AATCAAAGAGGCTCT | 55743 |
rs181349929 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | CHFR | GRCh38.p7 | 12:132846512 | CTTGACCTCATGATC[C/T]GCCCGCCTCAGCCTC | 55743 |
rs181455609 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132855852 | GATAAAAGTTTCAAG[C/T]GTTTTTTTTTGTCGT | 55743 |
rs181461646 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132880732 | AGCACGTTGGGAGGC[C/T]GAGGCGGGCGGATCA | 55743 |
rs181488501 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | CHFR | GRCh38.p7 | 12:132879070 | AGTGCAGTGGCACCA[A/T]CTCGGCTCACCACAA | 55743 |
rs181555253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132850156 | GATGGGATTTCACCA[C/T]GTTAGCCAGGATGGT | 55743 |
rs181632183 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132862173 | CCAGCTACTCAAGAG[C/G]CTGAGGCAGAAAAAT | 55743 |
rs181685454 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132847411 | GGTGTGAATGAGACA[A/T]GAAAGCCAGGCCACA | 55743 |
rs181756096 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132881330 | GACAAGCTATGGACT[A/G]GTGGAAATATTTGTA | 55743 |
rs181760612 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132866730 | CATTGGAATGTTACA[C/G]GAATGTTACAACACA | 55743 |
rs181881227 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132879306 | GGCCTGCGATAGGCA[C/T]TTGTACACGTATAAG | 55743 |
rs181964126 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132862536 | TTGAGCCCGGGAGTT[C/G]GAGGCTACAGTGAGC | 55743 |
rs182092641 | snp | A/G | 1.65089e-05 | 0.00287301 | missense | CHFR | GRCh38.p7 | 12:132857465 | GGTTTTTACAGATCC[A/G]CTCCACGGGACAGCG | 55743 |
rs182104463 | snp | A/G | 0 | 0 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132840603 | GCAAAGCTAGCACAG[A/G]CGGAAGCCAAGGTGC | 55743 |
rs182174483 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132875879 | TCCATAAAACACCGT[A/T]AGTGAAAAAAGCTGG | 55743 |
rs182186155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132870095 | CGGTGGCTCATACCT[A/G]TAATCCCAGCACTTT | 55743 |
rs182337163 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CHFR | GRCh38.p7 | 12:132889448 | AAAAGGTGTAAAACC[A/G]GCTGGGCGCAGTGGC | 55743 |
rs182337416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132872846 | GCTCTGGGCAGAAGC[A/G]GACTAAATGCTGGGC | 55743 |
rs182447560 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886504 | GACAGGACCAGCGCA[C/T]TTCTCTCCCCATACA | 55743 |
rs182450521 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132853977 | TGGGAGCCACACCAG[G/T]CGCCTGCAAAGCCCC | 55743 |
rs182464502 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CHFR | GRCh38.p7 | 12:132850929 | CCATGAAATAAAGGA[C/T]AAGCTCCATTTTTAA | 55743 |
rs182465400 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132882204 | CCACAGAACACTACC[C/T]GGTAACAGAAAGGAG | 55743 |
rs182480047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132867241 | GCCCAGAGAGCGTGA[A/G]AGGTTTCTGGTTTCA | 55743 |
rs182483420 | snp | A/G | 0.000352827 | 0.0132774 | intron-variant | CHFR | GRCh38.p7 | 12:132848765 | CGCACTCAGCGCTGA[A/G]GGCTGTCTCCAACAC | 55743 |
rs182713534 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132844527 | CTGACCTCGTGATCC[A/G]CCCGCCTCGGCCTCC | 55743 |
rs182783233 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132879739 | CTTGCCCTCTCCTTA[A/C]ATCAAAAGAACAAAG | 55743 |
rs182786381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132863726 | TCATAACGACAGGAA[C/T]GACCTTGGCAGAAAA | 55743 |
rs182791160 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | CHFR, LOC101928530 | GRCh38.p7 | 12:132888282 | AACGCGCCAATGTCT[C/G]CACTCATGAGGAGCC | 55743 |
rs182899775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132877120 | GTTTTTTTCAACAGA[C/T]GCATATACGATAGGA | 55743 |
rs182916402 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132841323 | TGCTGATGCCACCAC[A/G]AGCCCTGCCCAGCGC | 55743 |
rs183016641 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132879468 | CGATCTCAGCTCACT[A/G]CAACCTCTGCCTCCC | 55743 |
rs183017419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132883027 | CATTCTAATCTGGAA[C/T]CGAGATGCTTTGTGC | 55743 |
rs183023680 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132867893 | AAAAATCTCAAAAAG[A/G]TTTTTCTATTAAACT | 55743 |
rs183025987 | snp | A/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132844508 | CCAGGATGGTCTCGA[A/T]CTCCTGACCTCGTGA | 55743 |
rs183190682 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CHFR | GRCh38.p7 | 12:132858809 | GTCAGCCAGGCATAG[C/T]GGTGTGCACCTGTAG | 55743 |
rs183198904 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | CHFR | GRCh38.p7 | 12:132839979 | TCAGCCTCGCCCCTG[C/T]ACTAACTCAGAACCT | 55743 |
rs183240079 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132852102 | CATTCTCCTGCTTTA[A/G]CCTCCCGAGTAGCTG | 55743 |
rs183445120 | snp | A/G | 0.199564 | 0.24486 | intron-variant | CHFR | GRCh38.p7 | 12:132844491 | GGGTTTCACCGTGTT[A/G]GCCAGGATGGTCTCG | 55743 |
rs183473929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132871481 | TAAAAAATTAAATAA[A/G]TAAGTATTGGCCAGG | 55743 |
rs183497077 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CHFR | GRCh38.p7 | 12:132878338 | GCTGGGCATGGTGGC[A/G]GTTGCCTATAATCCC | 55743 |
rs183514686 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | CHFR | GRCh38.p7 | 12:132843223 | TAACTAGTTTCCTCG[C/G]ACCGTTCTGAGATTT | 55743 |
rs183626521 | snp | A/G | 0.00011707 | 0.00764991 | intron-variant | CHFR | GRCh38.p7 | 12:132856743 | AGGAGGGGTCTGGGC[A/G]GACCGCCCTCACGTG | 55743 |
rs183800755 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132872138 | AACAGACACTATTCA[C/T]GGCAGGAACCCATGT | 55743 |
rs183823752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132848932 | ATCCCTGAAAAAAGG[C/T]GAGGCTCACATTTTC | 55743 |
rs183840138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132875158 | TAATCTGATATCTAT[C/T]AGACTAGGAAACGGA | 55743 |
rs183981990 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | CHFR, LOC101928530 | GRCh38.p7 | 12:132888482 | ACAAACCATATATAC[A/G]CACATATATACATAT | 55743 |
rs183988735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132853321 | GGGCCCAAAGGGGGC[A/G]AGCAGTGCAGACAGG | 55743 |
rs184081725 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CHFR | GRCh38.p7 | 12:132850066 | TCACGCCATTCTCCT[A/G]CCTCAGCCTCCCAAG | 55743 |
rs184158541 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CHFR | GRCh38.p7 | 12:132885148 | GGCGCGATAGCTCAC[A/G]CCTGTAATCCCAGCA | 55743 |
rs184176169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132884075 | TAGTGAGTGAAGATC[A/G]CACCACTGCACTCCA | 55743 |
rs184200761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132849285 | AACTGAACATTTACA[A/G]GCGTGATGCACTGCA | 55743 |
rs184305709 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132880739 | TGGGAGGCCGAGGCG[A/G]GCGGATCACAAGGTC | 55743 |
rs184328661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132868230 | GGCGCGGCAGCTCAC[A/G]CCTGTAATCCTAGCA | 55743 |
rs184378969 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132859437 | CTCACTGCAAGCTCC[A/G]CCTCCCGGGTTCATG | 55743 |
rs184393013 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132866554 | ATGTTACAACACACC[A/G]CGATTGTTACAACAC | 55743 |
rs184400529 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | CHFR | GRCh38.p7 | 12:132846600 | AAAAACAACCTGAAG[G/T]CCGGGCATAGTGGCT | 55743 |
rs184471258 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132842492 | CCATCACTTTAATCT[C/G]AACTCCTTGGGCCAC | 55743 |
rs184496603 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132880652 | AACAGAGCAAGACTC[C/T]GACTCAAAAAAAGAA | 55743 |
rs184518193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132846472 | AGACAGGGTTTTACC[A/G]TGTTAGCCAGGATGG | 55743 |
rs184540886 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886206 | AGTCCCAGCTACTCC[C/G]AGGCTGAGGCGGGAG | 55743 |
rs184613283 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132880182 | TATAGTAAACAATAC[A/C]GTATTGTGGCTGTGT | 55743 |
rs184619249 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132864781 | GCGTAAGCCACCACA[A/C]CCGGCCAGAAGAATT | 55743 |
rs184628119 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CHFR | GRCh38.p7 | 12:132845021 | AGTATGTCTTGAAAA[C/T]CAAATTGCACAGAGG | 55743 |
rs184702348 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CHFR | GRCh38.p7 | 12:132855189 | GAATGTTGCAGTGGG[C/T]GAAGGTCATGCCACT | 55743 |
rs184741050 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CHFR | GRCh38.p7 | 12:132878884 | GTATCTTAATTTAGT[C/T]CTTAATTTCTTTTCT | 55743 |
rs185052974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132854087 | GTAGGAAAAAATACA[C/T]GAGGCTCTCCTCTCC | 55743 |
rs185091976 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | CHFR | GRCh38.p7 | 12:132855229 | CCTGGGCAACAGAGC[A/G]AGACTTTGTCTCGAA | 55743 |
rs185146508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132873101 | ACCCGACACACAAAA[C/T]GGCAACCGGGCAAAA | 55743 |
rs185196528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132869356 | CCACTGAAATGTACA[C/T]TTCGGCTGGATGACT | 55743 |
rs185310827 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132850332 | GTCTTATAACGCCTA[C/T]GACCACTTCACCAAT | 55743 |
rs185318326 | snp | A/G | 3.72322e-05 | 0.00431447 | intron-variant | CHFR | GRCh38.p7 | 12:132877667 | AACCTAAAAAAGAGA[A/G]GGTGGGTCAACACGG | 55743 |
rs185426568 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, nc-transcript-variant | CHFR, LOC101928530 | GRCh38.p7 | 12:132888245 | ACGCGTCCACGCAGG[A/G]GGAGTCTGTGCGGTT | 55743 |
rs185430843 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132871307 | AAATACAAAAATTAG[C/G]CGGGTGTGGTGGTGT | 55743 |
rs185444868 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132851810 | GTTAGAGAGGCCGCC[A/G]GGAAGCACAGCGAGG | 55743 |
rs185548279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132874511 | GAACAGGTGGGAAGG[C/T]CCAGGACCAGCACCC | 55743 |
rs186043486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132867155 | CGAACAGGAGAGGTG[C/T]GGCTGCCCGTGTGAA | 55743 |
rs186085029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132848356 | AAAAAGATCAGCTCT[C/T]CGAGTCTCCCCAGCA | 55743 |
rs186095846 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | CHFR | GRCh38.p7 | 12:132862262 | CCTGGGCAACAAGAG[C/T]GAAACTCCCTCTGGG | 55743 |
rs186108492 | snp | C/T | 0.0156354 | 0.0870243 | intron-variant | CHFR | GRCh38.p7 | 12:132844185 | TCTTCCCAACAGCAG[C/T]GCACGGACTTCACAG | 55743 |
rs186170072 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132881973 | GCAAAATGGACAAGC[A/G]CATGGGAAACAATGC | 55743 |
rs186188885 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CHFR | GRCh38.p7 | 12:132879074 | CAGTGGCACCATCTC[A/G]GCTCACCACAACCTC | 55743 |
rs186309849 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132875482 | CCCCATCTGAGCTAG[A/G]CGTGGCGGCGGGCAC | 55743 |
rs186340199 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132843686 | AAGAAAAGAGTGCTG[C/G]CCGAGCGTGGTGGCT | 55743 |
rs186407885 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | CHFR | GRCh38.p7 | 12:132857144 | GAGGGACAGCCCTCA[C/T]GTGCCCGGGTGCTGC | 55743 |
rs186414040 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CHFR | GRCh38.p7 | 12:132881639 | TTGGGAGGCCGAGGC[A/G]GGCGGATCACATGGT | 55743 |
rs186414211 | snp | A/G | | | downstream-variant-500B | CHFR | GRCh38.p7 | 12:132840009 | TCCCTGCTCAGCCTC[A/G]CCCCTACACAAACTC | 55743 |
rs186492863 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132855914 | CCAACATTCAGACCC[C/T]GGTCTTGTGCATTAG | 55743 |
rs186527358 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132879325 | TACACGTATAAGAAA[C/T]TGCATCTTATATACA | 55743 |
rs186699691 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CHFR | GRCh38.p7 | 12:132874980 | AGGCCCTGATGTAGG[C/T]GGGAAAGCCCAGGAC | 55743 |
rs186710929 | snp | C/G | 0.00597247 | 0.0543191 | downstream-variant-500B | CHFR | GRCh38.p7 | 12:132839902 | CTGCTCAGCCTCACC[C/G]CTGCACAAACTTGGG | 55743 |
rs186843086 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CHFR | GRCh38.p7 | 12:132871559 | GGTGGATCACCTGAG[G/T]TCGGGAGTTTGAGAC | 55743 |
rs186850436 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | CHFR | GRCh38.p7 | 12:132849316 | CCCGGCCTCAGACCC[A/G]TATCGTTTCTTAAAC | 55743 |
rs186864702 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132876856 | CTGGAGTGCAGTGGT[A/G]CCATCTCAGCTCACC | 55743 |
rs186871527 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132858215 | ATACAAAAAAATTAG[C/T]CAGATGTGGTGACGC | 55743 |
rs186997492 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | CHFR | GRCh38.p7 | 12:132889456 | TAAAACCGGCTGGGC[A/G]CAGTGGCTCACGTCT | 55743 |
rs187000584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132873024 | CTCCTGGGGACTTCT[A/G]AGCAGAGACCTGACA | 55743 |
rs187003485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132854035 | TTGTACTTCCAAAAA[C/T]GAGCAGATAAAAATG | 55743 |
rs187037560 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | CHFR, LOC101928530 | GRCh38.p7 | 12:132888405 | TCGAGCCCAGGAGTT[C/G]GAGATTAGCCTGAGA | 55743 |
rs187057600 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CHFR | GRCh38.p7 | 12:132852430 | ACAAAGGACAGCCAC[C/G]GTGCACAAGACCAAT | 55743 |
rs187103175 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | CHFR | GRCh38.p7 | 12:132882326 | CACGCTGGAAGCAGC[A/C]GAAGGCAAAGAAACC | 55743 |
rs187115991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132867329 | TACACAGAGAGACAT[A/G]AAAACAAGGAGTGTC | 55743 |
rs187139452 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132848853 | GGTCTCATGGAAATC[A/G]GGGCGGGGCCACATC | 55743 |
rs187168951 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132848015 | AACACCAATAGAATG[C/T]AGAGAACCAGCTGGC | 55743 |
rs187354846 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886823 | AAAGACTTATTTGAC[A/C]CACCGGTTGCTTTAA | 55743 |
rs187360088 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132866961 | ATCACTTGAACCCGG[A/G]AGGCGGAGGTTGCAG | 55743 |
rs187362294 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132851025 | AGACAGGATTTCCCT[C/T]TGTCGCCAAGGCTGG | 55743 |
rs187432269 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132879835 | TAGAAGACAAAAAAG[C/T]GAAGGGTTTGGTCAG | 55743 |
rs187435653 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132864160 | TTACAGTATTCAAAT[A/G]TAAGTGTTATTATTT | 55743 |
rs187438733 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | CHFR | GRCh38.p7 | 12:132844875 | TGTCCTCAGATGATC[C/T]GCCCGCCTCGGCTTC | 55743 |
rs187609210 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132844498 | ACCGTGTTAGCCAGG[A/C]TGGTCTCGATCTCCT | 55743 |
rs187614517 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CHFR | GRCh38.p7 | 12:132870123 | TTTGGGAGGCTGAGG[C/T]GGGTAGATCACGAGG | 55743 |
rs187637749 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CHFR | GRCh38.p7 | 12:132868425 | ACCCAGGAGAATGGC[A/G]TGGGAGGCGGAGCTT | 55743 |
rs187667016 | snp | A/C | 0.00199481 | 0.0315187 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132840741 | AAGGGAGCAGCACGT[A/C]CTGGGACCTGCGTCC | 55743 |
rs187816091 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | CHFR | GRCh38.p7 | 12:132879627 | ATCTCTTGACCTCGT[A/G]ATATGCCCGCCTCGG | 55743 |
rs187817084 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132884443 | ACATATATATATATA[A/T]AATAAATAAATAAAA | 55743 |
rs187933172 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | CHFR | GRCh38.p7 | 12:132880431 | GGAGGCCAAGGGGGG[G/T]GCGGATCACAAGGTC | 55743 |
rs187936610 | snp | C/T | 0.167158 | 0.235875 | intron-variant | CHFR | GRCh38.p7 | 12:132844512 | GATGGTCTCGATCTC[C/T]TGACCTCGTGATCCA | 55743 |
rs187999239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132853371 | ACGTGCACGTCAGCA[C/T]CGGGCACAGCCACAA | 55743 |
rs188070626 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132871273 | CCTGGCCAACACGGC[A/G]AAACCCTGTCTGTAC | 55743 |
rs188083214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132878572 | GGGGTTGGCTAGGTC[C/T]GGTGGCTCACACCGA | 55743 |
rs188113510 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | CHFR | GRCh38.p7 | 12:132863305 | CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGACC | 55743 |
rs188170704 | snp | C/T | 0.000399281 | 0.0141238 | missense | CHFR | GRCh38.p7 | 12:132859174 | CGTGGACGGTTTGGG[C/T]ATTTCTACGCGGTTG | 55743 |
rs188370749 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132842246 | CAAGCTGGATGGCCT[A/G]TGGCCACCTTCCCTC | 55743 |
rs188442512 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132855544 | TGGTGGCATGCGCCT[C/G]TAGTCCCAGCTACTC | 55743 |
rs188455393 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132877128 | CAACAGACGCATATA[A/C]GATAGGAGTCCCACA | 55743 |
rs188596077 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CHFR | GRCh38.p7 | 12:132883330 | ACTCTGGATGCTGAG[A/G]AAGGAGAATCACTTG | 55743 |
rs188618682 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132849187 | CTCCTGGCTTCAAGG[C/G]ATCCTCCCACCTCAG | 55743 |
rs188840466 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886182 | CCAGGCATGGTGGCG[C/T]ACGCCTGTAGTCCCA | 55743 |
rs188859103 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | CHFR | GRCh38.p7 | 12:132850067 | CACGCCATTCTCCTG[A/C]CTCAGCCTCCCAAGT | 55743 |
rs188891986 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132867989 | TGTATAGCGCGATCC[A/C]ATTTAGAGAATCCAT | 55743 |
rs188955426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132864938 | GGAAACAATTTTACT[A/G]GTGAAGTTTGTTTTC | 55743 |
rs188963320 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | CHFR, LOC101928530 | GRCh38.p7 | 12:132888604 | CTGAGTCTCTCAACG[C/G]CAAAGTTAATCTGAA | 55743 |
rs188988732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132881030 | CCATCACTTTGGGTG[A/G]CCAAGGCGGGCGGAT | 55743 |
rs189002458 | snp | A/C | 0.00359711 | 0.0422566 | intron-variant | CHFR | GRCh38.p7 | 12:132866624 | AGAAAGTTACAACAC[A/C]CCGCGTAACACCAAA | 55743 |
rs189010161 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132846760 | TGGCACATGCCTGTA[A/G]TCCCAGCTACTCAGG | 55743 |
rs189121495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132843226 | CTAGTTTCCTCGGAC[C/T]GTTCTGAGATTTCAG | 55743 |
rs189143543 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | CHFR | GRCh38.p7 | 12:132878068 | TGGCCTCCCAAAGTG[C/T]TGAGATTACAGGCGT | 55743 |
rs189147856 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | CHFR | GRCh38.p7 | 12:132859638 | AACAGGTGTGAGCTA[A/C]CGCGCCCCACCCTCT | 55743 |
rs189157601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132842874 | ATAAAGGAAGAGCAG[A/G]ATTTCTAAATGAAGA | 55743 |
rs189161221 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CHFR | GRCh38.p7 | 12:132872147 | TATTCACGGCAGGAA[A/C]CCATGTGAGCAAGAA | 55743 |
rs189254612 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132845222 | GCACTTTGGGAGGCC[A/G]AGGCAGGCGGATCAC | 55743 |
rs189356957 | snp | A/G | | | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886968 | ATATTGCATTCTGGA[A/G]AGTATATGAACACAA | 55743 |
rs189385898 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132846482 | TTACCGTGTTAGCCA[G/T]GATGGTCTCAATCTC | 55743 |
rs189397497 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | CHFR | GRCh38.p7 | 12:132861133 | AAGTGATTCTCCTGC[C/T]TTGGCCTCCCAGTGT | 55743 |
rs189467243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132880722 | CTGTAATCTCAGCAC[A/G]TTGGGAGGCCGAGGC | 55743 |
rs189477910 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132874530 | GGACCAGCACCCAGC[A/G]CGGGGAAGCCAGGCC | 55743 |
rs189494389 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | CHFR | GRCh38.p7 | 12:132855215 | CCACTGCACTCCAGC[C/T]TGGGCAACAGAGCGA | 55743 |
rs189635956 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132851388 | ATAGACACAGATCCA[A/C]GCCGAGCCCCCGGTG | 55743 |
rs189658271 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132866025 | ACTCATAAATTTAAG[A/G]TTATGATGTTAAAAC | 55743 |
rs189755163 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132861892 | AGATGTCTGTGACCA[A/G]GCTTAGCCCTCGAGC | 55743 |
rs189888906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132878902 | TAATTTCTTTTCTGT[A/G]TAAACTTAGGTTTCA | 55743 |
rs189927815 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132873787 | TGGAGCCAATCCCCC[C/G]AGATGCCGAGGGGCG | 55743 |
rs189987561 | snp | A/G | 0.00011724 | 0.00765548 | synonymous-codon | CHFR | GRCh38.p7 | 12:132848657 | ACAAAACGGGGCCAG[A/G]CAGCCGTAGCAGCCG | 55743 |
rs190012213 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132843746 | CCGAGGTCAAGAGTT[C/T]GAGACCAGCCTGGCC | 55743 |
rs190134545 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB, nc-transcript-variant | CHFR, LOC101928530 | GRCh38.p7 | 12:132888272 | GGTTTGGAGGAACGC[A/G]CCAATGTCTGCACTC | 55743 |
rs190142905 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CHFR | GRCh38.p7 | 12:132851904 | CTGCCACCCAAACTC[A/G]GGGAGTCAAAACAGA | 55743 |
rs190192756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132850480 | GTTCTCTGTGGCTTC[C/T]CACCTGCCCTCCCAC | 55743 |
rs190271333 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886282 | ACCACTGCACCCCAG[C/T]CTGGGCCACAGAGCA | 55743 |
rs190292857 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CHFR | GRCh38.p7 | 12:132854159 | CAATAAGGCCAACAG[A/G]TAAGACCCAACCAGG | 55743 |
rs190479001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132882474 | AAAAGGTGAATTTTA[C/T]TACAAGTAAATGATA | 55743 |
rs190484921 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132867403 | GTCTTCTGGGAGACA[C/T]GGCTCTTGCTGCTGC | 55743 |