SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs190495847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132848914 | GTGATGGCGAGGAGT[C/T]GTATCCCTGAAAAAA | 55743 |
rs190534118 | snp | A/G/T | 0.00795532 | 0.062565 | intron-variant | CHFR | GRCh38.p7 | 12:132870075 | TTAGCCAGGCGTGCC[A/G/T]GGCGCGGTGGCTCAT | 55743 |
rs190690213 | snp | A/G | 0.167158 | 0.235875 | intron-variant | CHFR | GRCh38.p7 | 12:132844506 | AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTCGT | 55743 |
rs190908272 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CHFR | GRCh38.p7 | 12:132879242 | CCTCTTGATCCACCC[A/G]CCTCAGCCTCCCAAA | 55743 |
rs190910189 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, synonymous-codon | CHFR | GRCh38.p7 | 12:132862340 | GCTCACACCTGTAAT[C/G]ACAATACTTTGGGAG | 55743 |
rs190918008 | snp | A/G | 0.210301 | 0.246828 | intron-variant | CHFR | GRCh38.p7 | 12:132844486 | AGACTGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 55743 |
rs191042547 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | CHFR | GRCh38.p7 | 12:132882081 | AAATGTATGTCCCTA[C/G]AAAGACTGCACACTT | 55743 |
rs191056260 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132875515 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 55743 |
rs191062458 | snp | A/G | 3.30158e-05 | 0.00406286 | synonymous-codon | CHFR | GRCh38.p7 | 12:132857433 | GAGGTATGCTTCCAC[A/G]AGGTTGTTGAGGATG | 55743 |
rs191072646 | snp | C/T | 0.00398564 | 0.0444627 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132840540 | ACAAAAGATAAAAAA[C/T]TTTTTTTTCCAAAAA | 55743 |
rs191208449 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CHFR | GRCh38.p7 | 12:132863460 | CAGCGAACGAAGTTC[A/G]CGCCATTGCACTCCA | 55743 |
rs191398233 | snp | A/G | 0.00122017 | 0.0246698 | intron-variant | CHFR | GRCh38.p7 | 12:132872432 | TTTATTCTACTTAAA[A/G]TAACTTGGAGTTACA | 55743 |
rs191413650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132853378 | CGTCAGCACCGGGCA[C/T]AGCCACAAAGTGACT | 55743 |
rs191431354 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132879641 | TGATATGCCCGCCTC[A/G]GCTTCTCAAAGTGCT | 55743 |
rs191485801 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CHFR | GRCh38.p7 | 12:132875006 | AGGACCAGCACCCAG[C/T]GTGGAGAAGCCAGGC | 55743 |
rs191555164 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | CHFR | GRCh38.p7 | 12:132868581 | GCTACTCGGGAGGCT[A/G]AGGCAGGAGAATGGC | 55743 |
rs191561057 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132849597 | TGCACATATTCAGGT[A/G]GCTTTTTTTTTTTTT | 55743 |
rs191561526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132876935 | GAGTAGCTGGGATTA[C/T]AGGCGCATGCCACAA | 55743 |
rs191705887 | snp | A/T | 0.167158 | 0.235875 | intron-variant | CHFR | GRCh38.p7 | 12:132844515 | GGTCTCGATCTCCTG[A/T]CCTCGTGATCCACCC | 55743 |
rs191734535 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | CHFR, LOC101928530 | GRCh38.p7 | 12:132888462 | TAGGCATCCATTTGT[A/G]TAAAACAAACCATAT | 55743 |
rs191741891 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132855921 | TCAGACCCCGGTCTT[C/G]TGCATTAGGAAACCT | 55743 |
rs191846572 | snp | C/T | | | upstream-variant-2KB | CHFR | GRCh38.p7 | 12:132889546 | GCTAAGCCATCGCAT[C/T]CCCTGTGACCTGCAT | 55743 |
rs191849035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132853315 | AGGCCAGGGCCCAAA[A/G]GGGGCGAGCAGTGCA | 55743 |
rs191861587 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CHFR | GRCh38.p7 | 12:132873063 | GGTGTTGGTCAGGTG[A/G]CCAAGATCCAAGAGC | 55743 |
rs191998331 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886205 | TAGTCCCAGCTACTC[A/C]GAGGCTGAGGCGGGA | 55743 |
rs192003511 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132866966 | TTGAACCCGGGAGGC[A/G]GAGGTTGCAGTGAGC | 55743 |
rs192139476 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132871938 | CTCCAAAAGCAGAAC[C/T]ATCAATGGCCTCCAG | 55743 |
rs192226209 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | CHFR | GRCh38.p7 | 12:132880147 | AAGACTCATATTACT[G/T]AACTGACTTACCATC | 55743 |
rs192239061 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132864779 | AGGCGTAAGCCACCA[C/T]ACCCGGCCAGAAGAA | 55743 |
rs192247563 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132844954 | GGATATAAAATTTAA[A/T]TATTAAAACTCCCAA | 55743 |
rs192274031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132880518 | AAAAAATTAGCTGGG[C/T]GTGATGGCGGGCGCC | 55743 |
rs192283276 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CHFR | GRCh38.p7 | 12:132845808 | AACTGACCCCAGGAC[C/T]TCTGGATAGACAAGT | 55743 |
rs192336178 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132881725 | ACAAAAAAATTAGCC[A/G]GGCATGGTGGCACGT | 55743 |
rs192432877 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132885147 | GGGCGCGATAGCTCA[C/T]GCCTGTAATCCCAGC | 55743 |
rs192459248 | snp | A/G | 0.000429007 | 0.0146397 | intron-variant | CHFR | GRCh38.p7 | 12:132848080 | AGCCCGCAGCGAGTC[A/G]GTACCTTCAGGATGT | 55743 |
rs192495200 | snp | A/G | 3.83693e-05 | 0.00437986 | missense | CHFR | GRCh38.p7 | 12:132843048 | GAGTGCGGCAGTTAC[A/G]GCCCCAGTAGCAGTC | 55743 |
rs192574973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132858411 | CTACATGGCGAAACC[A/G]TCTCTACAAAAAACA | 55743 |
rs192590649 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | CHFR | GRCh38.p7 | 12:132878097 | GTGAGCCACCGCGCC[C/T]GGCCCATCCTGAACC | 55743 |
rs192592309 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | CHFR | GRCh38.p7 | 12:132860615 | CAGCAATGCTTCTAC[A/C]ATAACATTCCCAAAT | 55743 |
rs192688176 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132865145 | AACGCTGTGGGCCAC[A/G]CTGGAGCGGCCGGAA | 55743 |
rs192844482 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132841268 | AAAACTGCCCCTCTC[A/G]GCGGGACGGCCGCAT | 55743 |
rs192881942 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132877321 | ACACCATCTAGGTTT[C/G]TTTAAGTATACTCCA | 55743 |
rs192892496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132842376 | TCTTCCATGTGCTGT[C/T]TGTGCTCAAACACAA | 55743 |
rs192912972 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132854036 | TGTACTTCCAAAAAC[A/G]AGCAGATAAAAATGT | 55743 |
rs192962720 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132854382 | CCAGTCACACTCTGT[G/T]ACTCGACTGCTTCAC | 55743 |
rs193100032 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CHFR | GRCh38.p7 | 12:132868117 | AGGTAAGAGTCATGC[C/T]GTAAGGAACAGCATC | 55743 |
rs193118310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132859298 | CAGGTCAAGGTCCCC[A/G]TCCACAGGAGAAAGG | 55743 |
rs193183619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132874424 | GGACCAGCACCCAGC[A/G]CGGGGAAGCCAGGTC | 55743 |
rs193256644 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CHFR | GRCh38.p7 | 12:132849265 | CAGACCCACATCGTT[C/T]CTTAAACTGAACATT | 55743 |
rs193270151 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132868518 | AAACAAACAAACAAA[A/C]AACAAAAAAAAATTA | 55743 |
rs193277226 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132883865 | TGGCTGTAATCCCAA[A/C/T]GCTTTGGGAGGCCAA | 55743 |
rs199523285 | in-del | -/ATATATATATAT | | | intron-variant | CHFR | GRCh38.p7 | 12:132850965 | ACTGTATGTGTGTGC[-/ATATATATATAT]ATATATATATATATA | 55743 |
rs199541016 | in-del | -/TAT | | | intron-variant | CHFR | GRCh38.p7 | 12:132850266 | TGGAAATCCCTAAAA[-/TAT]AATGTTAGGTAAACC | 55743 |
rs199543220 | in-del | -/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132867969 | AAAATAAAAAAAAAA[-/T]AATATGTATAGCGCG | 55743 |
rs199698283 | in-del | -/A | | | intron-variant | CHFR | GRCh38.p7 | 12:132862278 | AAACTCCCTCTGGGG[-/A]AAAAAAAAATAAAAA | 55743 |
rs199736176 | in-del | -/A | | | intron-variant | CHFR | GRCh38.p7 | 12:132878474 | ACTCCAACTGGAAAT[-/A]AAAAAAAAAAAAAGC | 55743 |
rs199740623 | in-del | -/AAAC | | | intron-variant | CHFR | GRCh38.p7 | 12:132846884 | AGACTCCATCTCAAA[-/AAAC]AAACAAACAAACAAA | 55743 |
rs199754919 | snp | A/C | 1.70006e-05 | 0.00291548 | intron-variant | CHFR | GRCh38.p7 | 12:132857362 | TGGTGGTGGAGGGAC[A/C]GCCCTCACGTGCCCG | 55743 |
rs199758706 | snp | G/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132880195 | ACAGTATTGTGGCTG[G/T]GTAAGGATGGCCAGA | 55743 |
rs199761208 | snp | C/T | 8.23947e-05 | 0.00641799 | missense | CHFR | GRCh38.p7 | 12:132859165 | TGACGTCCTCGTGGA[C/T]GGTTTGGGCATTTCT | 55743 |
rs199790262 | snp | A/C/T | 0.00113074 | 0.0237557 | synonymous-codon, intron-variant | CHFR | GRCh38.p7 | 12:132869746 | CTGAGTGGCGGGCGA[A/C/T]GACGGAGGGACCCGG | 55743 |
rs199808935 | in-del | -/ACAG | 0.0501905 | 0.150254 | upstream-variant-2KB, downstream-variant-500B | CHFR, LOC101928530 | GRCh38.p7 | 12:132888720 | AGCGTCGACGTTAAA[-/ACAG]ACAACTTAAGGCTGA | 55743 |
rs199870613 | snp | A/G | 0.000127701 | 0.00798963 | intron-variant | CHFR | GRCh38.p7 | 12:132848199 | GTTTATAATGATGTC[A/G]CAGGAAAGCACTGTC | 55743 |
rs199908697 | snp | C/T | 8.89166e-05 | 0.00666711 | intron-variant | CHFR | GRCh38.p7 | 12:132851599 | GAACCCGCCTGCGTG[C/T]GGTGGCGCGGGCACT | 55743 |
rs199919075 | snp | C/G | 0.00460039 | 0.0477392 | intron-variant | CHFR | GRCh38.p7 | 12:132861644 | CAGACCCTGTGAGAG[C/G]AATCAAACAAGATAG | 55743 |
rs199978810 | in-del | -/C | 0.0810805 | 0.184299 | intron-variant | CHFR | GRCh38.p7 | 12:132877835 | TGAGACGGAGTCTCG[-/C]TCTGTCGCCCAGGCT | 55743 |
rs200049101 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132878768 | GAGCTTGCAGTGAGC[C/T]GATATGGCGCCACTG | 55743 |
rs200187965 | snp | A/T | 0.00199801 | 0.0315439 | missense | CHFR | GRCh38.p7 | 12:132847094 | GGCTCTCGGTCAACA[A/T]GTTTTTCCATGTCAA | 55743 |
rs200193965 | in-del | -/AGGTGATCCAA | | | intron-variant | CHFR | GRCh38.p7 | 12:132877029 | TGAGCTCCTGACCTC[-/AGGTGATCCAA]CTGCCTCAGCCTCCC | 55743 |
rs200213031 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon | CHFR | GRCh38.p7 | 12:132861528 | GGGTTCCAACGACGA[A/G]AAGGACGCAGTCTTT | 55743 |
rs200264810 | in-del | -/A | | | intron-variant | CHFR | GRCh38.p7 | 12:132868782 | CAGGGGCTGGGGGGA[-/A]GGGGACATGGGGAGT | 55743 |
rs200283117 | snp | C/G | 1.64914e-05 | 0.00287149 | synonymous-codon | CHFR | GRCh38.p7 | 12:132872391 | AATCACTGTTCCACT[C/G]GTGCTGTAAAAAAAC | 55743 |
rs200302708 | snp | A/G | 0.00557044 | 0.0524804 | intron-variant | CHFR | GRCh38.p7 | 12:132856662 | ACAGCGCCATTCACC[A/G]GCAGTGAGACATGGC | 55743 |
rs200436687 | snp | C/T | 0.00138368 | 0.0262664 | missense | CHFR | GRCh38.p7 | 12:132851633 | ACTGCTGAGGGGCGA[C/T]ACGCGGGTCCTGCTC | 55743 |
rs200438195 | snp | C/G | 0.00199792 | 0.0315431 | splice-acceptor-variant | CHFR | GRCh38.p7 | 12:132859228 | GGTCAAGGTCCCCAT[C/G]TACAGGAGAAAGGGA | 55743 |
rs200441646 | snp | A/C | 0.00199792 | 0.0315431 | missense | CHFR | GRCh38.p7 | 12:132841566 | TGCTTAGTTTTTGAA[A/C]CTTGTCTGTTCACAG | 55743 |
rs200445257 | snp | A/G | 1.64988e-05 | 0.00287213 | intron-variant | CHFR | GRCh38.p7 | 12:132841644 | GAGCATTGGAGAGGC[A/G]ATCAAATAAATTACA | 55743 |
rs200523839 | in-del | -/A | 0.245631 | 0.249962 | intron-variant | CHFR | GRCh38.p7 | 12:132868521 | AAACAAACAAAAAAC[-/A]AAAAAAAAATTAGCT | 55743 |
rs200569655 | in-del | -/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132866335 | TGTTACAACACACCA[-/G]AATGTTACAACACAC | 55743 |
rs200573883 | in-del | -/TC | | | intron-variant | CHFR | GRCh38.p7 | 12:132865652 | TGCTGGGATTACAGG[-/TC]TTTTTTTTTTTTTTT | 55743 |
rs200655603 | snp | C/T | 3.4046e-05 | 0.00412576 | intron-variant | CHFR | GRCh38.p7 | 12:132872424 | AAACACAATTTATTC[C/T]ACTTAAAATAACTTG | 55743 |
rs200727311 | in-del | -/A | | | intron-variant | CHFR | GRCh38.p7 | 12:132854216 | TTCATAAGGAAAAAA[-/A]TGTAAATGAAAATGA | 55743 |
rs200755284 | snp | A/G | 0.000140245 | 0.00837275 | intron-variant | CHFR | GRCh38.p7 | 12:132851608 | TGCGTGCGGTGGCGC[A/G]GGCACTCACACTGCT | 55743 |
rs200764395 | snp | A/G | 0.000148245 | 0.00860815 | missense | CHFR | GRCh38.p7 | 12:132856591 | GTGATTTTATTTCTG[A/G]CATCCATACTTTGCA | 55743 |
rs200833531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132871684 | GGCTGAGGCAGGAGA[A/G]TTGCTTGAACCCGGC | 55743 |
rs200838500 | snp | A/C | 0.00199808 | 0.0315444 | intron-variant | CHFR | GRCh38.p7 | 12:132851558 | GCCAACACCGCTTTG[A/C]AACCTGACCCCTGAA | 55743 |
rs200853567 | snp | G/T | 1.65002e-05 | 0.00287225 | missense | CHFR | GRCh38.p7 | 12:132848148 | ACACTTGTCACCCAG[G/T]TTGAGCTCTGCCGAG | 55743 |
rs200863145 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132879395 | TGGGATTTTTTTTTT[C/T]TTTTTTTTTTTTTGA | 55743 |
rs200914011 | in-del | -/GTTTTTGTTTG | | | intron-variant | CHFR | GRCh38.p7 | 12:132878999 | TTTGTTTTTTTTTTT[-/GTTTTTGTTTG]TTTTTTTTTTTTTGA | 55743 |
rs201026008 | in-del | -/AT | | | intron-variant | CHFR | GRCh38.p7 | 12:132850265 | ATGGAAATCCCTAAA[-/AT]ATAATGTTAGGTAAA | 55743 |
rs201040324 | in-del | -/CACCCACTT | | | intron-variant | CHFR | GRCh38.p7 | 12:132858921 | CCACTCCACCCACTC[-/CACCCACTT]ATCTGGGTGACAGAG | 55743 |
rs201058448 | snp | A/G | 3.29565e-05 | 0.00405921 | missense | CHFR | GRCh38.p7 | 12:132872288 | CCTCTCTCTTACTGT[A/G]TTCCGGTTCATTCTT | 55743 |
rs201082581 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132875322 | TACTGCTAGAAGACC[A/C]CCTGCCACTTGCAGC | 55743 |
rs201192149 | snp | C/T | 1.65067e-05 | 0.00287282 | missense | CHFR | GRCh38.p7 | 12:132861598 | CTTGCCACAGAGGGA[C/T]CACTTCCTTTAGGGG | 55743 |
rs201192402 | snp | A/G | 0.00132143 | 0.0256704 | intron-variant | CHFR | GRCh38.p7 | 12:132857596 | TGTCCAGACAGTCCC[A/G]CAGATGCAACCGCGA | 55743 |
rs201207249 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132860980 | CTGGTCTTGAACTCC[C/T]GACCTCAGATGATCC | 55743 |
rs201237898 | snp | G/T | 0.000399281 | 0.0141238 | missense | CHFR | GRCh38.p7 | 12:132848709 | AGGTGGCAGAAAGGC[G/T]GCAGGCAGACCGCAC | 55743 |
rs201350082 | snp | A/G | 0.000639665 | 0.0178724 | missense | CHFR | GRCh38.p7 | 12:132848721 | GGCTGCAGGCAGACC[A/G]CACCTGTGGAGAGAG | 55743 |
rs201381869 | snp | C/T | 0.000115453 | 0.00759693 | intron-variant | CHFR | GRCh38.p7 | 12:132841635 | TACACAAGAGAGCAT[C/T]GGAGAGGCAATCAAA | 55743 |
rs201415596 | in-del | -/TGA | | | intron-variant | CHFR | GRCh38.p7 | 12:132868804 | ATGGGGAGTGACTGC[-/TGA]TGGGGCCGAGGGGAA | 55743 |
rs201416333 | in-del | -/GACTTGGT | | | intron-variant | CHFR | GRCh38.p7 | 12:132845784 | CAAGTCCCCGAGGGT[-/GACTTGGT]CCCAGGACAACTGAC | 55743 |
rs201454195 | snp | C/T | 6.8285e-05 | 0.00584276 | missense | CHFR | GRCh38.p7 | 12:132851635 | TGCTGAGGGGCGACA[C/T]GCGGGTCCTGCTCGC | 55743 |
rs201463746 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132848599 | TTCACCAAGAGAACA[C/T]GCAAAGGTCAAAGCA | 55743 |
rs201486163 | in-del | -/GTTACAACACACCAGAAA | | | intron-variant | CHFR | GRCh38.p7 | 12:132866578 | ACAACACACCAGAAT[-/GTTACAACACACCAGAAA]GTTACAACACACCAG | 55743 |
rs201503848 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CHFR | GRCh38.p7 | 12:132880618 | AGCCAAGATGGTGCC[A/G]CTGCACTCCAGCCTG | 55743 |
rs201512224 | snp | A/G | 0.00057573 | 0.0169568 | intron-variant | CHFR | GRCh38.p7 | 12:132859255 | GGGATGTGTTCTGTC[A/G]TAACCAAGAAGGAAA | 55743 |
rs201537399 | snp | A/G | 0.00043774 | 0.0147878 | intron-variant | CHFR | GRCh38.p7 | 12:132851761 | CACGCACATTCAGCC[A/G]GAGCACGTGGGACCC | 55743 |
rs201625605 | snp | C/T | 0.000198522 | 0.009961 | intron-variant | CHFR | GRCh38.p7 | 12:132851570 | TTGAAACCTGACCCC[C/T]GAAGGACAGATAGGA | 55743 |
rs201692885 | in-del | -/CAA | 0.0138799 | 0.0821421 | intron-variant | CHFR | GRCh38.p7 | 12:132868679 | AGCGAGACTCCGTCT[-/CAA]CAACAACAAAAAAGA | 55743 |
rs201727566 | snp | G/T | 0.000399281 | 0.0141238 | missense | CHFR | GRCh38.p7 | 12:132861542 | AAAAGGACGCAGTCT[G/T]TCTGTCTGGGAGAGC | 55743 |
rs201794553 | in-del | -/CCTCTAT | | | intron-variant | CHFR | GRCh38.p7 | 12:132842067 | TCAGCTGAGATCACA[-/CCTCTAT]ACTCCAGCCTGGCAG | 55743 |
rs201828860 | snp | C/T | 0.000312935 | 0.0125048 | missense | CHFR | GRCh38.p7 | 12:132856546 | TCATCAGAAAAAGAC[C/T]GCCTGACTTTGGGCT | 55743 |
rs201884962 | snp | A/C | | | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886373 | AAGGGGTGAAATTAA[A/C]CAAAAAAAAAAAAAA | 55743 |
rs201932889 | in-del | -/A | | | intron-variant | CHFR | GRCh38.p7 | 12:132867958 | AATAGCTAAGAAAAT[-/A]TAAAAAAAAATAATA | 55743 |
rs202008784 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132863148 | TGATCCACCCACCTC[A/G]GCCTCCCAAAGTGCT | 55743 |
rs202105666 | snp | C/G/T | 3.29534e-05 | 0.00405904 | missense, intron-variant | CHFR | GRCh38.p7 | 12:132870745 | ATTCTTGTGTCATGC[C/G/T]TTGCTTTTCACTTAA | 55743 |
rs202138339 | snp | G/T | | | downstream-variant-500B | CHFR | GRCh38.p7 | 12:132840327 | GAAGTGAGGCAGCCC[G/T]AGACACGAGCCCAAC | 55743 |
rs202150771 | in-del | -/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132845469 | TCTCAAAAAAAAAAA[-/T]AAATAAATAAATAAA | 55743 |
rs367620504 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132841352 | GCTCACCAGGAGGGC[A/G]GGCTGCGGCCCCCGG | 55743 |
rs367672905 | snp | A/C | 0.000118623 | 0.00770048 | intron-variant | CHFR | GRCh38.p7 | 12:132857366 | GGTGGAGGGACCGCC[A/C]TCACGTGCCCGGGTG | 55743 |
rs367716640 | snp | C/T | 3.29766e-05 | 0.00406045 | intron-variant | CHFR | GRCh38.p7 | 12:132841611 | CCTGCAGGGAGAAAA[C/T]GGCCAAATTACACAA | 55743 |
rs367768726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132846816 | ACCCAGGAGGCCGAG[A/G]GGGCCTTGAGCTGAG | 55743 |
rs367930156 | snp | C/T | 0.000437904 | 0.0147905 | intron-variant | CHFR | GRCh38.p7 | 12:132870840 | TGCAAACTGAGAACT[C/T]ATTTTTCTCTTCTGT | 55743 |
rs367968934 | snp | C/T | 8.52115e-05 | 0.00652675 | missense | CHFR | GRCh38.p7 | 12:132853493 | GGGGCTCCTGGCTCG[C/T]CCTCGGGTGCTGGGC | 55743 |
rs368007757 | in-del | -/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132858522 | TGAAGTCAGGAGTTC[-/C]AAGACTAGCCTGGCC | 55743 |
rs368057398 | snp | A/G/T | 0.000108465 | 0.00736354 | intron-variant | CHFR | GRCh38.p7 | 12:132857562 | GCAGGGCTGCAAACT[A/G/T]AAAGTGCAAGAGGAA | 55743 |
rs368066324 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132860903 | GATTACAGGCATGCA[C/G]CACCACACCCAGCTA | 55743 |
rs368070354 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132882990 | TACAGGCATGAGCCA[C/T]CGTGCCTGGCCTGAA | 55743 |
rs368105143 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CHFR | GRCh38.p7 | 12:132855560 | TAGTCCCAGCTACTC[A/G]AGAGGCTGAGGCAGG | 55743 |
rs368132419 | in-del | -/A | | | intron-variant | CHFR | GRCh38.p7 | 12:132884704 | GGACACAGCAAGAAA[-/A]GTGGCCACCTGCAAG | 55743 |
rs368155095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132866990 | AGTGAGCCGAGATTG[C/T]GCCACTGCACTCCAG | 55743 |
rs368200517 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132846356 | CAAGCTCCGCCTCCC[A/G]GGTTCACGCCATTCT | 55743 |
rs368254163 | snp | A/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132866576 | TTACAACACACCAGA[A/T]TGTTACAACACACCA | 55743 |
rs368265220 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132844564 | GCTGGGATTACAGGC[C/G]TGAGCCACTGCGCCC | 55743 |
rs368334043 | in-del | -/TAGTAAACAATA | | | intron-variant | CHFR | GRCh38.p7 | 12:132880169 | CTTACCATCATGCTA[-/TAGTAAACAATA]CAGTATTGTGGCTGT | 55743 |
rs368405665 | snp | C/T | 1.67167e-05 | 0.00289103 | missense | CHFR | GRCh38.p7 | 12:132857521 | TCCATCCAGCCCGAG[C/T]AGCAAGCCGCGCAGA | 55743 |
rs368453010 | in-del | -/C | 0.00438332 | 0.0466095 | intron-variant | CHFR | GRCh38.p7 | 12:132857123 | TCACGTGCCCGGGTG[-/C]TGGTGGAGGGACAGC | 55743 |
rs368530178 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132883591 | AATTAGCCGGGCATG[A/G]TGGCGGGTGCCTGTA | 55743 |
rs368540619 | snp | A/G | 1.92591e-05 | 0.00310309 | intron-variant | CHFR | GRCh38.p7 | 12:132859017 | TGCCCCACACGGGAC[A/G]AAGAACCTGCAGTGC | 55743 |
rs368546468 | snp | A/C/G | 5.89528e-05 | 0.00542895 | intron-variant | CHFR | GRCh38.p7 | 12:132877681 | AGGGTGGGTCAACAC[A/C/G]GGATATGATCGTGGT | 55743 |
rs368559901 | snp | A/C/G | 0.0023933 | 0.0345097 | intron-variant | CHFR | GRCh38.p7 | 12:132851840 | GAGAGGTGCACCTGA[A/C/G]ACAGCCGGGGAAGAA | 55743 |
rs368570990 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132864213 | TGGCTTACAGCAGCT[A/G]AAAGAAAACAGAATA | 55743 |
rs368629483 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132864786 | AGCCACCACACCCGG[C/G]CAGAAGAATTTTTTT | 55743 |
rs368692761 | snp | A/G | 3.29647e-05 | 0.00405971 | synonymous-codon, intron-variant | CHFR | GRCh38.p7 | 12:132870782 | ATAGAGGTATGCCAC[A/G]TCTAAAAGAAAATCA | 55743 |
rs368712051 | snp | C/G | 0.000153988 | 0.00877327 | intron-variant | CHFR | GRCh38.p7 | 12:132848634 | GGGCCTGAAGAGCCA[C/G]TATTACCACAAAACG | 55743 |
rs368755833 | snp | A/C | 0.000118533 | 0.00769755 | synonymous-codon | CHFR | GRCh38.p7 | 12:132853558 | AGGACACTGCCGGCA[A/C]ACGACGTATGGCTGG | 55743 |
rs368788828 | snp | A/G | 0.000193367 | 0.00983089 | missense, intron-variant | CHFR | GRCh38.p7 | 12:132869682 | AGGCCGAGGCTGTGG[A/G]GAAGAGGTCTGACGT | 55743 |
rs368830800 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132855113 | TGGGTGTGGTGGCAT[A/G]TGCCCGTAATCCCAG | 55743 |
rs368869394 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | CHFR, LOC101928530 | GRCh38.p7 | 12:132888841 | TTTAACATAGTTTTA[C/T]GTAGCCCTGCAAAAC | 55743 |
rs368874309 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132876713 | CAAAGTGTCACTAAG[C/T]GTCCCATCCTGGAAA | 55743 |
rs368879553 | snp | A/G | 0.00022735 | 0.0106594 | intron-variant | CHFR | GRCh38.p7 | 12:132859060 | GCCAAGGGTGAACAC[A/G]GTCGCACCTCACGCA | 55743 |
rs368940560 | snp | A/G | 0.000643495 | 0.0179258 | intron-variant | CHFR | GRCh38.p7 | 12:132848075 | TCCCCAGCCCGCAGC[A/G]AGTCGGTACCTTCAG | 55743 |
rs368950869 | snp | C/T | 3.19565e-05 | 0.00399715 | intron-variant | CHFR | GRCh38.p7 | 12:132844167 | AGTTACCCAGCAACA[C/T]CATCTTCCCAACAGC | 55743 |
rs369053005 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132882040 | GTGGCCCAGCAATTC[C/T]ATTCATAGTTACTTA | 55743 |
rs369063253 | snp | A/G | 6.58892e-05 | 0.00573936 | synonymous-codon | CHFR | GRCh38.p7 | 12:132856590 | AGTGATTTTATTTCT[A/G]GCATCCATACTTTGC | 55743 |
rs369102381 | snp | C/T | 3.31049e-05 | 0.00406834 | intron-variant | CHFR | GRCh38.p7 | 12:132870823 | AAAAGTGGTGGCCCC[C/T]GTGCAAACTGAGAAC | 55743 |
rs369142435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132846293 | TTTGAGACGGAGTCT[C/T]GCTCTGTCCCCCAGG | 55743 |
rs369154068 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132884185 | GCACTTTGGGAAGCC[A/G]AGGCGGGTGGATCAC | 55743 |
rs369247980 | in-del | -/CCT | | | intron-variant | CHFR | GRCh38.p7 | 12:132854251 | AGATTACCTACTTCT[-/CCT]TCTAAACTGGCAAAA | 55743 |
rs369258242 | snp | A/G | 5.18103e-05 | 0.00508945 | intron-variant | CHFR | GRCh38.p7 | 12:132843979 | GGCAGAAGCCAAGAA[A/G]CCAACCCAGACAGAA | 55743 |
rs369264314 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132862623 | TGAGACGGACTCTTG[C/T]TCTGTTGCCCAGGCT | 55743 |
rs369276239 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132883803 | TATAAATGGCAGGCA[C/T]ATCATTGCTTTAAAA | 55743 |
rs369298584 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132884103 | CCAGCCTGGGTGACA[C/G]AGTAAGACTCCGTCT | 55743 |
rs369303345 | snp | A/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132870194 | CATCTCTACTAAAAA[A/T]ACAAAAAATTAGCTG | 55743 |
rs369319311 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132875880 | CCATAAAACACCGTA[A/C]GTGAAAAAAGCTGGC | 55743 |
rs369343431 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132857972 | TTGCAGAGTTCACGG[C/G]GTCACACACGACCCA | 55743 |
rs369464193 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132858929 | CCCACTCCACCCACT[C/T]ATCTGGGTGACAGAG | 55743 |
rs369521765 | snp | A/C/G | 8.25913e-05 | 0.0064257 | intron-variant | CHFR | GRCh38.p7 | 12:132872251 | CGTGCACCCCCGTGC[A/C/G]GGTCTGACCCCGGCA | 55743 |
rs369526598 | snp | A/T | 1.65029e-05 | 0.00287248 | synonymous-codon | CHFR | GRCh38.p7 | 12:132859190 | ATTTCTACGCGGTTG[A/T]GCGACCAACAACTGC | 55743 |
rs369617038 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | CHFR | GRCh38.p7 | 12:132844174 | CAGCAACACCATCTT[C/T]CCAACAGCAGCGCAC | 55743 |
rs369699755 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132858790 | CATTAAAAAAAAAAA[A/G]AAAGTCAGCCAGGCA | 55743 |
rs369745799 | in-del | -/GACA | | | intron-variant | CHFR | GRCh38.p7 | 12:132847902 | AATACGGAAAAAACA[-/GACA]AACACCAATGGCATG | 55743 |
rs369762153 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132872688 | CCTCCTAGTGGACCC[A/G]GAGGCCTCGTCTACA | 55743 |
rs369767393 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132856061 | CTATAGGACTTTATA[C/G]TCGCTAGATCAACTA | 55743 |
rs369783816 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132864458 | TATGCATACACTTAG[A/G]CATACAGATAGAAGA | 55743 |
rs369798831 | in-del | -/AG | | | intron-variant | CHFR | GRCh38.p7 | 12:132863299 | ATCATCTGAGGTCAG[-/AG]GAGTTCGAGACCAGC | 55743 |
rs369891917 | snp | C/G | | | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132840753 | CGTCCTGGGACCTGC[C/G]TCCAGCCCCAGGCTC | 55743 |
rs369899407 | snp | A/T | 0.00016647 | 0.00912179 | intron-variant | CHFR | GRCh38.p7 | 12:132844024 | AAGTCGGGGGCTCCT[A/T]ACCTGGCAACTCGGA | 55743 |
rs369908385 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132862151 | GTGGTGGCGAGTGCA[C/T]GTAGTCCCAGCTACT | 55743 |
rs369914434 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132847684 | TAAATCCTAGAAACC[A/G]AGGTAGCTTCCTAGA | 55743 |
rs369917506 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132881769 | GCTACTCAGGAGGCT[C/G]AGGCAAGAGAATGGC | 55743 |
rs369947250 | snp | A/C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132858519 | CACCTGAAGTCAGGA[A/C/G]TTCAAGACTAGCCTG | 55743 |
rs369961753 | snp | A/C/T | 0.000264434 | 0.0114957 | intron-variant | CHFR | GRCh38.p7 | 12:132872250 | ACGTGCACCCCCGTG[A/C/T]GGGTCTGACCCCGGC | 55743 |
rs370078954 | snp | A/G | 5.34516e-05 | 0.00516943 | intron-variant | CHFR | GRCh38.p7 | 12:132851596 | TAGGAACCCGCCTGC[A/G]TGCGGTGGCGCGGGC | 55743 |
rs370103218 | snp | A/C/G/T | 0.000362999 | 0.0134682 | intron-variant | CHFR | GRCh38.p7 | 12:132848079 | CAGCCCGCAGCGAGT[A/C/G/T]GGTACCTTCAGGATG | 55743 |
rs370142100 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132882468 | CCCCAAAAAAGGTGA[A/C]TTTTACTACAAGTAA | 55743 |
rs370149987 | snp | C/G | 1.65373e-05 | 0.00287548 | intron-variant | CHFR | GRCh38.p7 | 12:132856422 | GTCACGGTTGTGATG[C/G]TCCTCTGGCTCACAC | 55743 |
rs370209943 | snp | C/T | 0.00874735 | 0.0655527 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132841429 | TCACCCCAGAGCACC[C/T]GTCGGAGACCCTGCG | 55743 |
rs370250880 | snp | C/G | 0.000100883 | 0.00710149 | intron-variant | CHFR | GRCh38.p7 | 12:132869611 | GACCTCATGAGATGT[C/G]ACCTCACCACAACTG | 55743 |
rs370251257 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132878247 | AAGCTGAGGTGAATG[A/G]ATCACGAGGTCAGGA | 55743 |
rs370262359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132873738 | GCTGGCTACGGGGCT[A/G]GAGTGTGCACGGACT | 55743 |
rs370302404 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132878424 | CAGTGAGCTGAGATC[A/G]CGCCACTGCACTCCA | 55743 |
rs370314942 | snp | A/C | | | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132841326 | TGATGCCACCACGAG[A/C]CCTGCCCAGCGCTCA | 55743 |
rs370348872 | snp | A/G | 3.47186e-05 | 0.00416631 | missense | CHFR | GRCh38.p7 | 12:132877646 | TGCTGGGGAAGGAAA[A/G]GTCGCAACCTAAAAA | 55743 |
rs370358776 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132883028 | ATTCTAATCTGGAAC[C/G/T]GAGATGCTTTGTGCT | 55743 |
rs370386571 | snp | G/T | 4.96496e-05 | 0.0049822 | missense | CHFR | GRCh38.p7 | 12:132857410 | CCTCACTTGCCTGGA[G/T]GCTGGATGAGGTATG | 55743 |
rs370390497 | snp | A/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132878473 | GACTCCAACTGGAAA[A/T]AAAAAAAAAAAAAAG | 55743 |
rs370399252 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132866880 | TACTAAAAATACAAA[A/C]ATTTTCTGGGCGTGG | 55743 |
rs370402623 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | CHFR | GRCh38.p7 | 12:132889305 | AAAAATAACAAAATA[A/G]AAACTTTGTCTCCCT | 55743 |
rs370419863 | snp | C/T | | | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886180 | AGCCAGGCATGGTGG[C/T]GCACGCCTGTAGTCC | 55743 |
rs370425697 | snp | A/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132885423 | CTCAAAAAATATATA[A/T]ATAAATAAATAAATA | 55743 |
rs370438384 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132857045 | GAGGGACCACCCTCA[C/T]GTGCCCGGGTGCTGG | 55743 |
rs370462959 | snp | A/G | 3.30748e-05 | 0.00406649 | intron-variant | CHFR | GRCh38.p7 | 12:132847011 | TGGACACTCACATGC[A/G]CCTTAGAGCAGGAGG | 55743 |
rs370484626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132877820 | TTTTTTTTTTTTTCT[C/T]GAGACGGAGTCTCGC | 55743 |
rs370484647 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132860378 | CCAAGTAGTTTACTA[A/G]ATTAAGTTGTGTGAC | 55743 |
rs370517411 | snp | A/C | 6.73809e-05 | 0.00580396 | missense | CHFR | GRCh38.p7 | 12:132861629 | AGATGCCACCACCCC[A/C]AGACCCTGTGAGAGG | 55743 |
rs370622205 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132877921 | CATTCTCCTGCCTCA[A/G]CCTCCAGAGTAGCTG | 55743 |
rs370736443 | snp | G/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132863785 | TTTTTTTTGAGACAG[G/T]GTCTCACTCTTCACC | 55743 |
rs370740796 | in-del | -/GGAGGTTGCAGTGAGC | | | intron-variant | CHFR | GRCh38.p7 | 12:132881815 | GAGGTTGCAGTGAGC[-/GGAGGTTGCAGTGAGC]TGAGATTGCGCCACT | 55743 |
rs370773285 | snp | C/G | 1.67206e-05 | 0.00289137 | intron-variant | CHFR | GRCh38.p7 | 12:132861443 | ACACGAGAGGACTGA[C/G]GACACACACAACCAG | 55743 |
rs370879757 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132872018 | GAACCCAAACCATCC[C/G]CATCAGTTTCTCCTT | 55743 |
rs370903025 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132846054 | TCTTCTTCCCCATGT[C/T]GCCTTTCCTTAAAAG | 55743 |
rs370921824 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132863481 | TTGCACTCCAGCCTG[A/G]GCAGTAAGATCAAAA | 55743 |
rs370975355 | snp | C/T | 0.24449 | 0.249939 | intron-variant | CHFR | GRCh38.p7 | 12:132844539 | TCCACCCGCCTCGGC[C/T]TCCCAAAGTGCTGGG | 55743 |
rs371092913 | snp | A/G | 0.000101312 | 0.00711658 | missense | CHFR | GRCh38.p7 | 12:132848677 | CGTAGCAGCCGGTCC[A/G]GGTGCAGCCCCAGTA | 55743 |
rs371281524 | snp | A/G | 8.24124e-05 | 0.00641868 | intron-variant | CHFR | GRCh38.p7 | 12:132856675 | CCGGCAGTGAGACAT[A/G]GCAGGCAGACACAGC | 55743 |
rs371352835 | snp | C/G/T | 3.30274e-05 | 0.0040636 | intron-variant | CHFR | GRCh38.p7 | 12:132848064 | TGGCTCCCGGCTCCC[C/G/T]AGCCCGCAGCGAGTC | 55743 |
rs371373485 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132870196 | TCTCTACTAAAAATA[A/C]AAAAAATTAGCTGGG | 55743 |
rs371401118 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132857239 | GTGTGGATGCCCTCA[C/T]GTGCCCGGGTGCTGG | 55743 |
rs371434249 | snp | A/G | 4.94368e-05 | 0.00497152 | synonymous-codon | CHFR | GRCh38.p7 | 12:132859154 | AGCCGCTGCTCTGAC[A/G]TCCTCGTGGACGGTT | 55743 |
rs371470066 | snp | A/G | 0.000437904 | 0.0147905 | missense, intron-variant | CHFR | GRCh38.p7 | 12:132869744 | ACCTGAGTGGCGGGC[A/G]ACGACGGAGGGACCC | 55743 |
rs371521075 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CHFR | GRCh38.p7 | 12:132842365 | ACAACATGGTCTCTT[C/T]CATGTGCTGTTTGTG | 55743 |
rs371541325 | snp | A/G | 0.000114384 | 0.00756167 | missense | CHFR | GRCh38.p7 | 12:132853523 | CAGTGGGGAGGCTGC[A/G]CCGCCTGCCTTCTGT | 55743 |
rs371671641 | snp | C/T | 0.000144129 | 0.00848784 | intron-variant | CHFR | GRCh38.p7 | 12:132851581 | CCCCTGAAGGACAGA[C/T]AGGAACCCGCCTGCG | 55743 |
rs371728915 | in-del | -/GCAACACCA | | | intron-variant | CHFR | GRCh38.p7 | 12:132844161 | ACAGCCAGTTACCCA[-/GCAACACCA]TCTTCCCAACAGCAG | 55743 |
rs371746589 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886501 | GTTGACAGGACCAGC[C/G]CATTTCTCTCCCCAT | 55743 |
rs371841032 | snp | C/T | 2.23142e-05 | 0.00334015 | missense | CHFR | GRCh38.p7 | 12:132843015 | GCTGCACTCACATGG[C/T]GTGGTGAGCTTTCAC | 55743 |
rs371886985 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132870135 | AGGCGGGTAGATCAC[A/G]AGGTCAGGAGATCGA | 55743 |
rs371908101 | snp | C/T | 0.000182156 | 0.00954174 | intron-variant | CHFR | GRCh38.p7 | 12:132857567 | GCTGCAAACTGAAAG[C/T]GCAAGAGGAACAGTG | 55743 |
rs372002721 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132855349 | ATCGCTTGAACCCGG[G/T]AGGCGGAGGTTGCAA | 55743 |
rs372011347 | snp | C/T | 0.000161121 | 0.00897412 | intron-variant | CHFR | GRCh38.p7 | 12:132861657 | AGGAATCAAACAAGA[C/T]AGGTGCTGATCCATC | 55743 |
rs372012714 | snp | C/T | 5.80131e-05 | 0.00538546 | missense | CHFR | GRCh38.p7 | 12:132848722 | GCTGCAGGCAGACCG[C/T]ACCTGTGGAGAGAGG | 55743 |
rs372093401 | snp | A/G | 0.00039992 | 0.0141351 | missense, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132887298 | AGGGCTGCGGCGGCG[A/G]CGACTGCTTGCCTTC | 55743 |
rs372139703 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132869362 | AAATGTACACTTCGG[A/C]TGGATGACTTTTATG | 55743 |
rs372224351 | snp | A/T | 1.6953e-05 | 0.0029114 | intron-variant | CHFR | GRCh38.p7 | 12:132844003 | GACAGAACTAGAGCC[A/T]TGAGGAAGTCGGGGG | 55743 |
rs372270460 | snp | A/G | 0.00011971 | 0.00773568 | missense | CHFR | GRCh38.p7 | 12:132853566 | GCCGGCACACGACGT[A/G]TGGCTGGCTGCAAGG | 55743 |
rs372386886 | snp | C/G | 1.64931e-05 | 0.00287163 | intron-variant | CHFR | GRCh38.p7 | 12:132856455 | TCTGCTCTGAGCCAG[C/G]GGCATGATTTACCTA | 55743 |
rs372404283 | snp | A/G | 4.94588e-05 | 0.00497262 | synonymous-codon | CHFR | GRCh38.p7 | 12:132848127 | GTTGTTCAGCACGCC[A/G]TCCAGACACTTGTCA | 55743 |
rs372489905 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132882314 | CCTGTGTCACGACAC[A/G]CTGGAAGCAGCAGAA | 55743 |
rs372547607 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132853316 | GGCCAGGGCCCAAAG[C/G]GGGCGAGCAGTGCAG | 55743 |
rs372554759 | snp | C/T | 0.000387607 | 0.0139159 | intron-variant | CHFR | GRCh38.p7 | 12:132851767 | CATTCAGCCGGAGCA[C/T]GTGGGACCCAGGGCA | 55743 |
rs372647321 | snp | A/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132875190 | CATCAGTTCTTCCTA[A/T]TAAAACCTACTTCCT | 55743 |
rs372698171 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132858550 | GCCAACATGGTGAAA[A/C/T]CCTGTCTCTACTAAA | 55743 |
rs372703275 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132845271 | CCAGCCTAACCAAGA[C/T]GGTGAAACCTCACCT | 55743 |
rs372954969 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132873711 | ACTTTCTGTGTCCTC[C/T]TGCTCCACAGGGCTG | 55743 |
rs373015296 | snp | C/T | 3.3189e-05 | 0.0040735 | intron-variant | CHFR | GRCh38.p7 | 12:132847137 | CAGGTAATTCTGTGA[C/T]GCAAAAAAAGAGAGG | 55743 |
rs373065688 | snp | G/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132874160 | CCATATCGGACTCTG[G/T]ACCTCCATAACTATA | 55743 |
rs373137192 | snp | C/T | | | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132840801 | CACAAGGGAGCAGCA[C/T]GTCCTGGGACCTGCG | 55743 |
rs373179194 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132874653 | GGGGAAGCCAGGCCC[C/T]GGAACAGGCGGGACT | 55743 |
rs373319220 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132882224 | ACAGAAAGGAGCAAA[C/T]TGCTCATCCATGCAA | 55743 |
rs373360706 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132849521 | CACCTGCTCCACCAC[C/T]CTAACACGGCTTCGA | 55743 |
rs373367991 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132885496 | ATGTAGTATTTTGCT[A/G]TGGTAGTATGAACAA | 55743 |
rs373380601 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132868424 | GACCCAGGAGAATGG[C/T]GTGGGAGGCGGAGCT | 55743 |
rs373411620 | snp | A/G | 4.97797e-05 | 0.00498873 | synonymous-codon | CHFR | GRCh38.p7 | 12:132844037 | CTTACCTGGCAACTC[A/G]GAAGCAGGAATGTTC | 55743 |
rs373528706 | snp | A/G | | | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132840763 | CCTGCGTCCAGCCCC[A/G]GGCTCGGGGCCGCGG | 55743 |
rs373530982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132866176 | CAGGTGGAAACTACA[C/T]AGCACTCACTCTCCA | 55743 |
rs373534148 | snp | A/T | | | upstream-variant-2KB, downstream-variant-500B | CHFR, LOC101928530 | GRCh38.p7 | 12:132888880 | GGGGGAAATCTACTT[A/T]GTAGAGAATCTCCTT | 55743 |
rs373536896 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132876940 | GCTGGGATTACAGGC[A/G]CATGCCACAACGCCC | 55743 |
rs373634619 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CHFR | GRCh38.p7 | 12:132853957 | GAGCGCGGTGGGCAA[C/T]GTACTGGGAGCCACA | 55743 |
rs373669694 | in-del | -/T | 0.35809 | 0.225425 | intron-variant | CHFR | GRCh38.p7 | 12:132852148 | GCCACGCCTGGCTAA[-/T]TTTTTTTTTTTTTGT | 55743 |
rs373678045 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132844371 | CTCACTGCAAGCTCC[A/G]CCTCCCGGGTTCACG | 55743 |
rs373682287 | in-del | -/ATAA | | | intron-variant | CHFR | GRCh38.p7 | 12:132885419 | TGTCTCAAAAAATAT[-/ATAA]ATAAATAAATAAATA | 55743 |
rs373754363 | snp | C/T | | | missense | CHFR | GRCh38.p7 | 12:132861511 | AAATCCTCCTGATCC[C/T]GGGGTTCCAACGACG | 55743 |
rs373793123 | in-del | -/A | | | intron-variant | CHFR | GRCh38.p7 | 12:132863545 | ACAAACAAAAAAAAA[-/A]CAGAAGTCTGTGTAA | 55743 |
rs373907187 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132883363 | CCTGGGAGGCGGAGG[C/T]TGCAGTGAGCCGAGA | 55743 |
rs373924283 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132868541 | AAAAATTAGCTGGGC[A/G]TGGTTGCAGGCACCT | 55743 |
rs373980352 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132866942 | AGGAGGCTGAGGCAG[A/G]GGAATCACTTGAACC | 55743 |
rs374006779 | snp | A/G | 0.00060109 | 0.0173258 | synonymous-codon | CHFR | GRCh38.p7 | 12:132853492 | TGGGGCTCCTGGCTC[A/G]CCCTCGGGTGCTGGG | 55743 |
rs374093971 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132877674 | AAAAGAGAGGGTGGG[C/T]CAACACGGGATATGA | 55743 |
rs374104668 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132857901 | CGTTCATTCTATGCG[A/G]AATACACCTTCCCAG | 55743 |
rs374107669 | snp | C/T | 1.64855e-05 | 0.00287097 | missense | CHFR | GRCh38.p7 | 12:132861578 | CAAAGCTGGAGACTT[C/T]ATCACTTGCCACAGA | 55743 |
rs374113719 | snp | G/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132844696 | AGTGCAGTGGCGGGG[G/T]CTCAGCTCACTGCAA | 55743 |
rs374115787 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CHFR | GRCh38.p7 | 12:132846220 | CCTCCCCTACAAGGA[C/T]AGAAGCTGCTGGAAT | 55743 |
rs374133871 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132875060 | GGACCAGCACCCAGC[A/G]TGGGGAAGCCAGGCC | 55743 |
rs374145324 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132872174 | AGAAATGGGGTGTAG[C/G]CAGGAGGAACGTTCC | 55743 |
rs374186901 | snp | A/G | 1.651e-05 | 0.0028731 | intron-variant | CHFR | GRCh38.p7 | 12:132872257 | CCCCCGTGCGGGTCT[A/G]ACCCCGGCAAGCCTT | 55743 |
rs374229656 | snp | A/G | 0.000690608 | 0.0185695 | missense | CHFR | GRCh38.p7 | 12:132853526 | TGGGGAGGCTGCGCC[A/G]CCTGCCTTCTGTACT | 55743 |
rs374367997 | in-del | -/ATAT | | | intron-variant | CHFR | GRCh38.p7 | 12:132850965 | ACTGTATGTGTGTGC[-/ATAT]ATATATATATATATA | 55743 |
rs374375176 | snp | C/T | 1.69284e-05 | 0.00290928 | intron-variant | CHFR | GRCh38.p7 | 12:132859254 | AGGGATGTGTTCTGT[C/T]GTAACCAAGAAGGAA | 55743 |
rs374414666 | snp | A/G/T | 0.000103024 | 0.00717654 | intron-variant | CHFR | GRCh38.p7 | 12:132859276 | AAGAAGGAAATACAC[A/G/T]CAGGTTCAGGTCAAG | 55743 |
rs374502930 | snp | C/T | 3.29527e-05 | 0.00405898 | synonymous-codon, intron-variant | CHFR | GRCh38.p7 | 12:132870737 | ACCAAAGGATTCTTG[C/T]GTCATGCCTTGCTTT | 55743 |
rs374524420 | snp | A/G | 0.000346692 | 0.0131615 | intron-variant | CHFR | GRCh38.p7 | 12:132848070 | CCGGCTCCCCAGCCC[A/G]CAGCGAGTCGGTACC | 55743 |
rs374575464 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132866416 | ACCGGAACACCACAC[C/G]GGAATGTTACAACAC | 55743 |
rs374602539 | snp | A/G | 6.61244e-05 | 0.0057496 | intron-variant | CHFR | GRCh38.p7 | 12:132848161 | AGGTTGAGCTCTGCC[A/G]AGATGAAGGGGCAAT | 55743 |
rs374666765 | snp | G/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132881463 | TTATCAAAGAAGAGA[G/T]ATGGATGGCAAATTA | 55743 |
rs374668913 | snp | C/T | 0.000188573 | 0.00970828 | intron-variant | CHFR | GRCh38.p7 | 12:132853423 | GGCCTGAGGGCGGCG[C/T]GGCTCACCTGTCGTC | 55743 |
rs374674144 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132876433 | TTTGATTCAGACATG[C/G]TCAACTGGTAAGTAT | 55743 |
rs374679777 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | CHFR | GRCh38.p7 | 12:132880427 | TTTGGGAGGCCAAGG[C/G]GGGGGCGGATCACAA | 55743 |
rs374685119 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132875931 | TGTAATCCCAGCACT[C/T]TGGGAGGCTGAGGCA | 55743 |
rs374696622 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132864199 | AAAACACAAGAAACT[G/T]GCTTACAGCAGCTGA | 55743 |
rs374707891 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132855039 | TTGAGGTCAGGATTT[C/T]GAGACCAGTCTGGCC | 55743 |
rs374746962 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132882856 | GACTACCAATATGCA[A/C]CACCACGCTCAGCTA | 55743 |
rs374767368 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CHFR | GRCh38.p7 | 12:132843178 | AACGACAGACGCTGC[A/G]GTGGAAACGCACGGC | 55743 |
rs374771830 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132883317 | TGTAATCCCAGCTAC[C/T]CTGGATGCTGAGGAA | 55743 |
rs374800280 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132870341 | TGGGCGACAAAGCGC[A/G]ACTCCATCTCAAAAA | 55743 |
rs374806207 | in-del | -/T | 0.499992 | 0.00199679 | intron-variant | CHFR | GRCh38.p7 | 12:132879010 | TTTTGTTTTTGTTTG[-/T]TTTTTTTTTTTTGAG | 55743 |
rs374833796 | snp | G/T | | | upstream-variant-2KB, downstream-variant-500B | CHFR, LOC101928530 | GRCh38.p7 | 12:132888745 | TAAGGCTGACCAAAC[G/T]GTCTGTAGCATTAAG | 55743 |
rs374912879 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132879228 | TCTTGAACTCCTGAC[C/G]TCTTGATCCACCCGC | 55743 |
rs374915350 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132854530 | CCCAGCTTCATAAAA[A/G]TATTTGTTTCTCATG | 55743 |
rs374924130 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132877928 | CTGCCTCAGCCTCCA[C/G]AGTAGCTGGGACTGC | 55743 |
rs375010018 | snp | C/G | | | upstream-variant-2KB, intron-variant | CHFR, LOC101928530 | GRCh38.p7 | 12:132888104 | CTGTTCTGAACGCGC[C/G]TAACTTTTGCCTCAG | 55743 |
rs375022775 | snp | A/C/G/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132880426 | CTTTGGGAGGCCAAG[A/C/G/T]GGGGGGCGGATCACA | 55743 |
rs375121053 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132870168 | CCAACCTGGCTAACA[C/T]GGTGAAACCCCATCT | 55743 |
rs375150375 | snp | C/T | 0.00018498 | 0.00961538 | intron-variant | CHFR | GRCh38.p7 | 12:132857609 | CCACAGATGCAACCG[C/T]GACCCTCGACCAAGG | 55743 |
rs375174098 | snp | C/T | 0.000131961 | 0.00812176 | missense | CHFR | GRCh38.p7 | 12:132859182 | GTTTGGGCATTTCTA[C/T]GCGGTTGTGCGACCA | 55743 |
rs375199215 | snp | A/G | 1.65029e-05 | 0.00287248 | synonymous-codon | CHFR | GRCh38.p7 | 12:132857445 | CACGAGGTTGTTGAG[A/G]ATGTGGTTTTTACAG | 55743 |
rs375322247 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CHFR | GRCh38.p7 | 12:132877960 | GGCGCCCGCCATCAC[A/G]CCTGGCTAATTTTTT | 55743 |
rs375336559 | snp | A/G | 0.000135842 | 0.0082403 | intron-variant | CHFR | GRCh38.p7 | 12:132853595 | GGAAGCACAGGGCCG[A/G]GCTGTGTGCAGGCCC | 55743 |
rs375400951 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132853025 | AGCCAACTCTGGTGA[C/T]GCAGGGCAGCTTCTG | 55743 |
rs375411000 | in-del | -/AA | | | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132841398 | TCACTCAGAGGGTAA[-/AA]AGCTCCACAGAAGAG | 55743 |
rs375414850 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132841885 | GCCGAGGCGGGCGGA[C/T]CACTTGAGGTCAGGA | 55743 |
rs375426809 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132879388 | GACACTTTGGGATTT[C/T]TTTTTTCTTTTTTTT | 55743 |
rs375465304 | in-del | -/TATACTC | | | intron-variant | CHFR | GRCh38.p7 | 12:132842071 | CTGAGATCACACCTC[-/TATACTC]CAGCCTGGCAGACAG | 55743 |
rs375476644 | snp | A/C | | | upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132887839 | CAGAAGGGACGGGGA[A/C]CTTCCGGATTGGAAG | 55743 |
rs375571065 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132857612 | CAGATGCAACCGCGA[C/T]CCTCGACCAAGGTCC | 55743 |
rs375656978 | snp | A/C/G | 0.000170192 | 0.00922344 | synonymous-codon | CHFR | GRCh38.p7 | 12:132848717 | GAAAGGCTGCAGGCA[A/C/G]ACCGCACCTGTGGAG | 55743 |
rs375659602 | snp | A/G | 2.032e-05 | 0.00318741 | intron-variant | CHFR | GRCh38.p7 | 12:132877688 | GTCAACACGGGATAT[A/G]ATCGTGGTAACTGTG | 55743 |
rs375664747 | snp | C/T | 0.000148298 | 0.00860971 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132841534 | TCCAGTGCTGAAAGC[C/T]GCTCAGGGCCTCTGG | 55743 |
rs375812260 | snp | C/T | 4.79191e-05 | 0.00489462 | intron-variant | CHFR | GRCh38.p7 | 12:132853421 | GAGGCCTGAGGGCGG[C/T]GCGGCTCACCTGTCG | 55743 |
rs375836961 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132864414 | TTTAGTAGCTGCTCA[A/G]TAAGCAGTAACTATA | 55743 |
rs375866802 | snp | C/T | 3.3065e-05 | 0.00406588 | intron-variant | CHFR | GRCh38.p7 | 12:132870816 | AAATCAGAAAAGTGG[C/T]GGCCCCTGTGCAAAC | 55743 |
rs375871219 | snp | A/G | 0.000405597 | 0.014235 | intron-variant | CHFR | GRCh38.p7 | 12:132869570 | AGGTAAAGAGTAGTG[A/G]ACAAAAACCATGCAA | 55743 |
rs375885289 | snp | C/T | 1.6537e-05 | 0.00287545 | intron-variant | CHFR | GRCh38.p7 | 12:132847008 | CCCTGGACACTCACA[C/T]GCGCCTTAGAGCAGG | 55743 |
rs376069713 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132885026 | CTGGAAGAGGGAAGT[C/T]GCAGTGAGCCGAGAT | 55743 |
rs376072720 | snp | C/T | 9.9941e-05 | 0.00706828 | intron-variant | CHFR | GRCh38.p7 | 12:132877685 | TGGGTCAACACGGGA[C/T]ATGATCGTGGTAACT | 55743 |
rs376073261 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132873786 | CTGGAGCCAATCCCC[A/C]CAGATGCCGAGGGGC | 55743 |
rs376095263 | snp | A/G | 0.000194463 | 0.00985868 | intron-variant | CHFR | GRCh38.p7 | 12:132844186 | CTTCCCAACAGCAGC[A/G]CACGGACTTCACAGC | 55743 |
rs376138583 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | CHFR, LOC101928530 | GRCh38.p7 | 12:132888343 | GACCGGGCGCAGTGA[C/T]TTACGCCTGTAATCT | 55743 |
rs376262240 | snp | A/G | | | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132840365 | CGGAGGAGCAAACGC[A/G]GCTCATTTATTAGAA | 55743 |
rs376296871 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132867397 | GGAGCAGTCTTCTGG[A/G]AGACATGGCTCTTGC | 55743 |
rs376297178 | snp | A/G | 0.000152759 | 0.00873819 | intron-variant | CHFR | GRCh38.p7 | 12:132857363 | GGTGGTGGAGGGACC[A/G]CCCTCACGTGCCCGG | 55743 |
rs376414001 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B | CHFR, LOC101928530 | GRCh38.p7 | 12:132888922 | TCTTTTCCTGATCCA[A/G]GAGAGAATGTAAGAC | 55743 |
rs376441897 | snp | A/C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132874423 | AGGACCAGCACCCAG[A/C/T]GCGGGGAAGCCAGGT | 55743 |
rs376516972 | in-del | -/A | | | intron-variant | CHFR | GRCh38.p7 | 12:132870532 | GCAAAACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 55743 |
rs376528866 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132877887 | GGCTCACTGCAAGCT[A/C]CGCCTCCCAGGTTCA | 55743 |
rs376544772 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132885595 | AAAAGATAAACTCAA[C/T]GACATATTTTCTCTC | 55743 |
rs376613134 | in-del | A/GG | | | intron-variant | CHFR | GRCh38.p7 | 12:132868383 | TAGTCCCAGCTACTC[A/GG]GAGGCTGAGGCAGGA | 55743 |
rs376637364 | in-del | -/CAGGAGAATGGCG | | | intron-variant | CHFR | GRCh38.p7 | 12:132868413 | AAAATGGCGTGGACC[-/CAGGAGAATGGCG]TGGGAGGCGGAGCTT | 55743 |
rs376676732 | in-del | -/AAT | | | intron-variant | CHFR | GRCh38.p7 | 12:132850269 | AAATCCCTAAAATAT[-/AAT]GTTAGGTAAACCCTC | 55743 |
rs376724917 | snp | A/C/G | 0.000584823 | 0.0170906 | intron-variant | CHFR | GRCh38.p7 | 12:132848057 | GAAAATGTGGCTCCC[A/C/G]GCTCCCCAGCCCGCA | 55743 |
rs376759624 | snp | A/G | 0.000153988 | 0.00877327 | intron-variant | CHFR | GRCh38.p7 | 12:132848760 | TTACACGCACTCAGC[A/G]CTGAGGGCTGTCTCC | 55743 |
rs376798546 | snp | A/G/T | 4.97305e-05 | 0.0049863 | missense | CHFR | GRCh38.p7 | 12:132844078 | GATAGGTCAGCTCAC[A/G/T]GAAGCTGCGCAGGCC | 55743 |
rs376798596 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132872604 | CTGACTGACAGCCTA[A/C]CCAGCCACTACACCT | 55743 |
rs376804846 | snp | C/T | 0.000205005 | 0.0101223 | intron-variant | CHFR | GRCh38.p7 | 12:132842986 | TCACTCTGTAGCTGA[C/T]GCCTGTGCCCCCAGC | 55743 |
rs376838234 | in-del | -/GGATTACAGGTGTGAATAA | | | intron-variant | CHFR | GRCh38.p7 | 12:132864071 | TACAGGTGTGAATAA[-/GGATTACAGGTGTGAATAA]CCTATATCTTAATAA | 55743 |
rs376917471 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132882304 | ACCCTGTGACCCTGT[A/G]TCACGACACGCTGGA | 55743 |
rs376925671 | snp | A/G | | | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132840769 | TCCAGCCCCAGGCTC[A/G]GGGCCGCGGTCACTC | 55743 |
rs376942538 | in-del | -/CTC | | | downstream-variant-500B | CHFR | GRCh38.p7 | 12:132839928 | TGGGACCTCCCCCTT[-/CTC]AGCCTCGCCCCTGCA | 55743 |
rs376948686 | snp | C/T | 8.37851e-05 | 0.0064719 | intron-variant | CHFR | GRCh38.p7 | 12:132851748 | GACTGCTGAAGCACA[C/T]GCACATTCAGCCGGA | 55743 |
rs376960803 | snp | C/T | 3.53139e-05 | 0.00420187 | intron-variant | CHFR | GRCh38.p7 | 12:132877540 | AACACCAAAAGAAGC[C/T]CAGAACATACTCACC | 55743 |
rs376980326 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132857201 | TGGTGGTGGAGGGAC[C/T]GCCCTCACGTGCCTG | 55743 |
rs376989159 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132848387 | CCTGGTCTTGGTATC[A/G]TAACAGCAGAACCCC | 55743 |
rs376995659 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132873602 | GGGCGCTGGAGCTGG[A/G]CTGACTTTCTGTGTC | 55743 |
rs377093117 | snp | A/G | 5.02854e-05 | 0.005014 | intron-variant | CHFR | GRCh38.p7 | 12:132844014 | AGCCATGAGGAAGTC[A/G]GGGGCTCCTTACCTG | 55743 |
rs377117671 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CHFR | GRCh38.p7 | 12:132852132 | GGGACTACAGGTGCC[C/T]GCCACGCCTGGCTAA | 55743 |
rs377169496 | in-del | -/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132845463 | TTCCATCTCAAAAAA[-/T]AAAAATAAATAAATA | 55743 |
rs377181821 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132866629 | GTTACAACACACCGC[A/G]TAACACCAAATGTTA | 55743 |
rs377203307 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132864764 | AAGTGCTGGGATTAC[A/C]GGCGTAAGCCACCAC | 55743 |
rs377225060 | snp | C/T | 1.6473e-05 | 0.00286988 | missense | CHFR | GRCh38.p7 | 12:132856598 | TATTTCTGGCATCCA[C/T]ACTTTGCACATCTTC | 55743 |
rs377284812 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132856789 | AGGGACTGCCCTCAC[A/G]TGCCCAGGTGCTGGT | 55743 |
rs377288948 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132879472 | CTCAGCTCACTGCAA[A/C]CTCTGCCTCCCGGGT | 55743 |
rs377307738 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132847647 | GCTCGGCAGGAGGGC[A/G]AATGCGCATGTTAAA | 55743 |
rs377318460 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon | CHFR | GRCh38.p7 | 12:132859208 | GACCAACAACTGCCC[A/G]TTCAGGTCAAGGTCC | 55743 |
rs377321183 | in-del | -/C | 0.237593 | 0.249692 | intron-variant | CHFR | GRCh38.p7 | 12:132846549 | TGCTGGGATTACAGG[-/C]GTGAGCCACCACACC | 55743 |
rs377469033 | snp | G/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132853939 | ACTCTCCCGTTAAAA[G/T]CAGAGCGCGGTGGGC | 55743 |
rs377537751 | snp | A/G | | | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132840795 | CACTCACACAAGGGA[A/G]CAGCATGTCCTGGGA | 55743 |
rs377621783 | snp | G/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132843330 | CTTTGGGAGGCAGAG[G/T]CAGGAGAATCGCTTG | 55743 |
rs377654552 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132877763 | GGATCCCCATTGTAC[A/G]TATGTAAAAAAAAAC | 55743 |
rs377655249 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132860101 | GCAGTCACCCTCCGT[C/T]TCAGCCGCTCCTCAC | 55743 |
rs377661913 | snp | A/G | 9.41176e-05 | 0.0068593 | intron-variant | CHFR | GRCh38.p7 | 12:132853422 | AGGCCTGAGGGCGGC[A/G]CGGCTCACCTGTCGT | 55743 |
rs377703818 | snp | A/C/G | 0.000148276 | 0.00860922 | missense | CHFR | GRCh38.p7 | 12:132872293 | CTCTTACTGTGTTCC[A/C/G]GTTCATTCTTCCTGT | 55743 |
rs386378317 | in-del | -/AA | | | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132841397 | CTCACTCAGAGGGTA[-/AA]AAGCTCCACAGAAGA | 55743 |
rs386768334 | multinucleotide-polymorphism | AAAATAAATAAAT/TAAAAAAATAAAA | | | intron-variant | CHFR | GRCh38.p7 | 12:132845465 | TCCATCTCAAAAAAA[AAAATAAATAAAT/TAAAAAAATAAAA]AAATAAAAATAAAAA | 55743 |
rs386768335 | multinucleotide-polymorphism | AT/TA | | | intron-variant | CHFR | GRCh38.p7 | 12:132845477 | AAAAAAATAAATAAA[AT/TA]AATAAAAATAAAAAA | 55743 |
rs397699952 | in-del | -/A | | | intron-variant | CHFR | GRCh38.p7 | 12:132881271 | CAAAAAAAAAAAAAA[-/A]GTAAAAATCTGTTCT | 55743 |
rs397710019 | in-del | -/G | 0 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132852459 | TCGATGTGGCAGCAG[-/G]AAGTCTGAGCCCACA | 55743 |
rs397724778 | in-del | -/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132852520 | ACAGGAAAGACCCTG[-/G]CGAGGTCAACATGCC | 55743 |
rs397826941 | in-del | -/A | 0 | 0 | downstream-variant-500B | CHFR | GRCh38.p7 | 12:132840328 | AGTGAGGCAGCCCCA[-/A]GACACGAGCCCAACA | 55743 |
rs397932561 | in-del | -/A | | | intron-variant | CHFR | GRCh38.p7 | 12:132855517 | AAAAATACAAAAAAA[-/A]TTAGCTGGGTGTGGT | 55743 |
rs397943123 | in-del | -/A | | | intron-variant | CHFR | GRCh38.p7 | 12:132876185 | CTCAAAAAAAAAAAA[-/A]GAAAGAAAGAAAAAA | 55743 |
rs398117032 | in-del | -/A | | | intron-variant | CHFR | GRCh38.p7 | 12:132884426 | TCTCAAAAAAAAAAA[-/A]TACATATATATATAT | 55743 |
rs527277947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132884702 | TGAGGACACAGCAAG[A/G]AAGTGGCCACCTGCA | 55743 |
rs527354484 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132883866 | GGCTGTAATCCCAAC[A/G]CTTTGGGAGGCCAAG | 55743 |
rs527369492 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132850906 | TCTGCAGGAATACAT[A/T]AAAACAGCCATGAAA | 55743 |
rs527434303 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132850393 | TTAGAGTGAAGAGTT[C/T]GGATTCCTGGGGAAA | 55743 |
rs527495567 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132855735 | ATTATGACACACGTA[A/T]GAATGGCTGGGTAGA | 55743 |
rs527509659 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132859645 | GTGAGCTACCGCGCC[C/T]CACCCTCTTCTGGTG | 55743 |
rs527512444 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | CHFR | GRCh38.p7 | 12:132862136 | AAAAATTAGACAGGC[G/T]TGGTGGCGAGTGCAT | 55743 |
rs527533791 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132877245 | GTACAGTAGCACGCT[A/G]TATAGGTTGATAGCC | 55743 |
rs527662045 | in-del | -/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132847827 | GGGAACAAGAGCTGC[-/G]GGGAAGCGGCTCCTA | 55743 |
rs527687528 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132866628 | AGTTACAACACACCG[A/C]GTAACACCAAATGTT | 55743 |
rs527745057 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132878081 | TGCTGAGATTACAGG[C/T]GTGAGCCACCGCGCC | 55743 |
rs527807607 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132877766 | TCCCCATTGTACATA[C/T]GTAAAAAAAAACACT | 55743 |
rs527905433 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132843907 | TGAGCCGAGATTGCA[C/G]CACTGCACTCCAGCC | 55743 |
rs527913981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132849789 | AAGATGGGGTCTCAC[C/T]GCGTTGGTCAGGCTG | 55743 |
rs527968667 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132855008 | GCACTTTGAGAGGCC[A/G]AGGCAGACGGATCAC | 55743 |
rs527987049 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | CHFR, LOC101928530 | GRCh38.p7 | 12:132888873 | GTCTCCTGGGGGAAA[C/T]CTACTTTGTAGAGAA | 55743 |
rs528028239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132854411 | ACGTCTAAACATTGA[C/T]GTCACTGCGCATGTG | 55743 |
rs528150645 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132859330 | ATGTGTTCTAACTGT[C/T]GTAACCGAGAAGGAA | 55743 |
rs528171380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132866097 | TAGTCTACAGGAGAC[A/G]GGCTAGTAGAAACTT | 55743 |
rs528230033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132871407 | CAGTGAGCTGAGATC[A/G]CGCCATTGCACTCCA | 55743 |
rs528352347 | in-del | -/AGG | 0.00398564 | 0.0444627 | intron-variant | CHFR | GRCh38.p7 | 12:132884325 | TCGGGAGGCTGAGGC[-/AGG]AGAATTGCTTGAACC | 55743 |
rs528362205 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132876660 | CTTATTTCTGAGACA[G/T]ACTTAATTTGAATAC | 55743 |
rs528398581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132843227 | TAGTTTCCTCGGACC[A/G]TTCTGAGATTTCAGG | 55743 |
rs528424126 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132875779 | TCAAAACAATAAATG[A/T]CCACCAATAAGGGAA | 55743 |
rs528442186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132881125 | TACAAAAAATTAGCC[A/G]GGCATGGTAGCATGC | 55743 |
rs528485306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132880882 | AGGCAGGAGAATGGT[A/G]GGAACCCAGGAAGCG | 55743 |
rs528531341 | snp | A/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132858195 | AACTCCCGTCTCTAC[A/T]AAAAATACAAAAAAA | 55743 |
rs528637661 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132852959 | CTTCCTGGATAGCAC[C/G]TGGAGCCCCTTGCTG | 55743 |
rs528650161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132858807 | AAGTCAGCCAGGCAT[A/G]GTGGTGTGCACCTGT | 55743 |
rs528701305 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132864716 | CTGGTCTTGAACTCC[C/T]GACCTCAGGCGATCC | 55743 |
rs528732651 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132868427 | CCAGGAGAATGGCGT[A/G]GGAGGCGGAGCTTGC | 55743 |
rs528759811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132864234 | AAACAGAATAGTTTT[A/G]GGGACAAACCACCTC | 55743 |
rs528767583 | snp | C/G | 0.00716266 | 0.059414 | upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132887761 | ATCTTTGATCCTGAC[C/G]AGGCGACTTCGTCGC | 55743 |
rs528820178 | snp | C/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | CHFR | GRCh38.p7 | 12:132889462 | CGGCTGGGCGCAGTG[C/G]CTCACGTCTGTAATC | 55743 |
rs528825047 | snp | C/T | 9.82849e-05 | 0.00700948 | synonymous-codon, intron-variant | CHFR | GRCh38.p7 | 12:132869671 | CTCCGTGGAAGAGGC[C/T]GAGGCTGTGGGGAAG | 55743 |
rs528837591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132855523 | TACAAAAAAATTAGC[C/T]GGGTGTGGTGGCATG | 55743 |
rs528899640 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132855149 | CGGGAGGCTAACACG[A/G]GAGAATCACTTGAAC | 55743 |
rs528938408 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CHFR | GRCh38.p7 | 12:132874574 | GACTGCCCAGGACCA[A/G]CACCCAGCGTGGGAA | 55743 |
rs528961539 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132860891 | CCAAGTAGCTGGGAT[C/T]ACAGGCATGCACCAC | 55743 |
rs528977296 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132854613 | AGTTCAAGACCATCC[C/T]GACTAACACGGTGAA | 55743 |
rs529039039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132866537 | ATGTTACAACACACC[A/G]GATGTTACAACACAC | 55743 |
rs529123840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132866229 | TCCCCAATTAGCACC[C/T]GAGAAGTCCTCCCAG | 55743 |
rs529251771 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132871217 | AGCACTCTGGGAGGC[C/T]GAGGCGGGCGGATTA | 55743 |
rs529253276 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CHFR | GRCh38.p7 | 12:132843777 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAACA | 55743 |
rs529282512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132876685 | GAATACATTCAAGAA[A/G]GGTCATAGACACCAA | 55743 |
rs529300705 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132843263 | AAACACATGTTTAAC[G/T]AAAAACCCAACTGAG | 55743 |
rs529301861 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132881823 | CAGTGAGCTGAGATT[C/G]CGCCACTGCAAATCC | 55743 |
rs529320977 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CHFR | GRCh38.p7 | 12:132881260 | GAGACTCCATCTCAA[A/G]AAAAAAAAAAAGTAA | 55743 |
rs529323260 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132872231 | ACGTTCAGAGAGCGC[C/T]CTCACGTGCACCCCC | 55743 |
rs529384430 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | CHFR, LOC101928530 | GRCh38.p7 | 12:132888063 | GACGCGGGGCCACGT[C/G]TTGGCCGGCGTTTTG | 55743 |
rs529458682 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CHFR | GRCh38.p7 | 12:132856064 | TAGGACTTTATAGTC[A/G]CTAGATCAACTACAA | 55743 |
rs529465232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132853888 | GGGCAAGGGCCAGCA[C/T]GTGCGCGCACGCCCC | 55743 |
rs529465307 | snp | C/T | 0.000755025 | 0.019415 | intron-variant | CHFR | GRCh38.p7 | 12:132848237 | CACTGAGGATAAACA[C/T]ATTTCTTTTCATTAC | 55743 |
rs529540046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132858820 | ATAGTGGTGTGCACC[C/T]GTAGTCCCAGCAACT | 55743 |
rs529541398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132850782 | GCGGCAGGAGCCAAC[C/T]GCGGTGCTCAACAGG | 55743 |
rs529547282 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132840433 | TGCTGCTTCTCAGTT[C/T]CTATCAAGAGCAAGA | 55743 |
rs529598415 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CHFR | GRCh38.p7 | 12:132864768 | GCTGGGATTACAGGC[A/G]TAAGCCACCACACCC | 55743 |
rs529643005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132870158 | GAGATCGAGGCCAAC[C/T]TGGCTAACACGGTGA | 55743 |
rs529705996 | snp | C/G | 9.40247e-05 | 0.00685591 | missense, intron-variant | CHFR | GRCh38.p7 | 12:132869784 | CCCCTCGCCCTGCAC[C/G]TGCACCTGAGGTATC | 55743 |
rs529733320 | in-del | -/AC | 0.00318978 | 0.0398085 | intron-variant | CHFR | GRCh38.p7 | 12:132879269 | CAAAGTGTTGGGATT[-/AC]AGGCTTGAGCCACCG | 55743 |
rs529824378 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | CHFR | GRCh38.p7 | 12:132864795 | ACCCGGCCAGAAGAA[-/T]TTTTTTTTTAATTAC | 55743 |
rs529824922 | in-del | -/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132877805 | AAAGACATAAAGAAA[-/T]TTTTTTTTTTTTCTT | 55743 |
rs529841762 | snp | A/G | | | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132885920 | CTCTTGTCTTAAAGG[A/G]ATAATTTTGATATGT | 55743 |
rs529921235 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886542 | CAGAGGAAATCAAAC[A/C]ACCAGATGGTCACTT | 55743 |
rs529928344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132841691 | AGGCATTCAAATAAA[C/T]GCATTCGGAAACCAT | 55743 |
rs529991788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132852069 | GCTCACTGCAAGCTC[C/T]GCCTCCCGGGTTCAC | 55743 |
rs530040541 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132885918 | TCCTCTTGTCTTAAA[C/G]GGATAATTTTGATAT | 55743 |
rs530063384 | snp | G/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132866556 | GTTACAACACACCGC[G/T]ATTGTTACAACACAC | 55743 |
rs530093842 | in-del | -/AG | | | intron-variant | CHFR | GRCh38.p7 | 12:132882060 | ATAGTTACTTAGCTA[-/AG]AGAAAAATGTATGTC | 55743 |
rs530114848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132857084 | CCACCCTCACGTGCC[C/T]GGGTGCTGGTGGAGG | 55743 |
rs530226230 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132883470 | GTGGCTCACGCCTCT[A/G]ATCCCAGCACTTTGG | 55743 |
rs530255889 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132868583 | TACTCGGGAGGCTGA[C/G]GCAGGAGAATGGCGT | 55743 |
rs530330334 | snp | G/T | 0.00636936 | 0.0560724 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132840914 | TTTGGACATTGGAAG[G/T]TTTCTTTTTTTAATA | 55743 |
rs530385569 | in-del | -/AT | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132883331 | TCTGGATGCTGAGGA[-/AT]AGGAGAATCACTTGA | 55743 |
rs530443967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132865423 | GCAGTGACGCGGTAT[C/T]GGCTCACTGCAACCT | 55743 |
rs530610656 | snp | A/G | 1.6504e-05 | 0.00287258 | intron-variant | CHFR | GRCh38.p7 | 12:132870693 | TATAGCTCCTAACAT[A/G]CACCCACTTCTTTGC | 55743 |
rs530627362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132875725 | TGAAGGCAGAGTTTG[A/G]GAAAGAGTCACTGCA | 55743 |
rs530675986 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132876594 | TTTGAGGGAAAGAAA[A/T]CAAACTTGAATAGGC | 55743 |
rs530735263 | in-del | -/G | 0.0162398 | 0.0886349 | intron-variant | CHFR | GRCh38.p7 | 12:132880425 | ACTTTGGGAGGCCAA[-/G]GGGGGGGCGGATCAC | 55743 |
rs530785070 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132847523 | CACACACGAGCTGTT[A/C/G]AGCTCCTTCTGTGGG | 55743 |
rs530841979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132852727 | CGCCAAGCACTGCTT[C/T]GTCCGTTCCGTCCAC | 55743 |
rs530852110 | in-del | -/A | | | intron-variant | CHFR | GRCh38.p7 | 12:132867970 | AAATTAAAAAAAAAT[-/A]ATATGTATAGCGCGA | 55743 |
rs530904066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132848402 | GTAACAGCAGAACCC[C/T]GCTGCAAGGATTCTG | 55743 |
rs530905027 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132866905 | GCGTGGTGGTGGTGC[A/G]CGCCTGTGACCCCAG | 55743 |
rs530906692 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886612 | TTCTCTCACCCGTTG[A/T]ATGACTTTGTTCAAG | 55743 |
rs531157221 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132874544 | CGCGGGGAAGCCAGG[A/C]CCCGGAACAGGCGGG | 55743 |
rs531161207 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132883675 | GAGCTTGCAGTGAGC[C/T]GAGATCGTGCCACTG | 55743 |
rs531259393 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132885759 | AAATCTATGAAGTAG[A/G]TACATAGGCGCAGAA | 55743 |
rs531300162 | snp | C/T | 1.64789e-05 | 0.0028704 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132841515 | AAAACACGCTCTCTT[C/T]ACCTCCAGTGCTGAA | 55743 |
rs531346228 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132884853 | GCACTTTGAGAGGCC[A/G]AGGCAGACAGATTGC | 55743 |
rs531499703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132862681 | GCCTCCTGGGTTGAC[A/G]CCATTCTCCTGCCTC | 55743 |
rs531555196 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132847397 | ACCTACACAGCCCAG[C/G]TGTGAATGAGACATG | 55743 |
rs531565509 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132863722 | AGAGTCATAACGACA[A/G]GAATGACCTTGGCAG | 55743 |
rs531629887 | in-del | -/A | | | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886390 | AAAAAAAAAAAAAAA[-/A]TTGCTTCCAAACAGC | 55743 |
rs531738863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132872668 | CTGGGTTCTCTCCCC[A/G]TTTGCCTCCTAGTGG | 55743 |
rs531761656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132878647 | ACACAGTGAAACCCC[A/G]TCTCTACTAAAAATA | 55743 |
rs531761855 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132872856 | GAAGCGGACTAAATG[C/T]TGGGCCGTCAGCTGC | 55743 |
rs531763057 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132879315 | TAGGCATTTGTACAC[A/G]TATAAGAAACTGCAT | 55743 |
rs531874913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132850326 | CCTTAAGTCTTATAA[C/T]GCCTACGACCACTTC | 55743 |
rs531943883 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132878196 | AATTTTACAGCCAGG[A/C]GCAGTGGCTCATACT | 55743 |
rs531943998 | in-del | -/AAAGA | 0.0142736 | 0.0832652 | intron-variant | CHFR | GRCh38.p7 | 12:132849496 | TGAGAGACACAAAAG[-/AAAGA]AATCTCACCTGCTCC | 55743 |
rs531984616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132883163 | CTGGGCGCGGTGGAT[C/T]ACACCTGTAATCCCA | 55743 |
rs531987562 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132875080 | GAAGCCAGGCCCTGA[A/C]GCAGGCGGGACAGCT | 55743 |
rs532140357 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132868775 | GCAGCTGCCAGGGGC[G/T]GGGGGGAGGGGACAT | 55743 |
rs532182592 | snp | A/C/T | 0.00636936 | 0.0560724 | intron-variant | CHFR | GRCh38.p7 | 12:132846516 | ACCTCATGATCCGCC[A/C/T]GCCTCAGCCTCCCAA | 55743 |
rs532199674 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132874612 | CCCCAGAACAGGCGG[G/T]ACTGCCCAGGACCAG | 55743 |
rs532242531 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CHFR | GRCh38.p7 | 12:132851938 | ACAATAACCAAAAAT[A/G]ATCTTTGATTTAGCA | 55743 |
rs532271996 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132857332 | CTGCTGGGTGGATGC[A/C]CTCACGTGCCTGGGT | 55743 |
rs532299302 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132845971 | TCCTTGCTCTTGTTA[C/T]CCAATAAATATGAAG | 55743 |
rs532332282 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132857039 | CTGGTGGAGGGACCA[A/C]CCTCACGTGCCCGGG | 55743 |
rs532405243 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132881821 | TGCAGTGAGCTGAGA[C/T]TGCGCCACTGCAAAT | 55743 |
rs532483070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132868252 | ATCCTAGCACTTTGG[A/G]AGGCCGATCGGACAG | 55743 |
rs532493761 | in-del | -/A | | | intron-variant | CHFR | GRCh38.p7 | 12:132880793 | AACATGGTGAAACCC[-/A]GTCTCTACTAAAAAT | 55743 |
rs532547167 | in-del | -/AA | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132850859 | AAATTAGGAAGTCAT[-/AA]AAAAAAAAGGCAAAG | 55743 |
rs532675767 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | CHFR | GRCh38.p7 | 12:132839972 | TCCCTGCTCAGCCTC[A/G]CCCCTGCACTAACTC | 55743 |
rs532675798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132845371 | GGCTGAGGCAGGACA[A/G]TTGTTGAACCTGGGA | 55743 |
rs532738902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132844834 | GATGGGGTTTCACCA[C/T]GTTGGCCAGGCTGGT | 55743 |
rs532744666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132873159 | TGCAGCTTCACTCCC[A/G]AGGCCCCAGCAGTGG | 55743 |
rs532886868 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132878337 | AGCTGGGCATGGTGG[C/T]GGTTGCCTATAATCC | 55743 |
rs532896158 | snp | A/T | 3.41233e-05 | 0.00413043 | intron-variant | CHFR | GRCh38.p7 | 12:132859269 | CGTAACCAAGAAGGA[A/T]ATACACGCAGGTTCA | 55743 |
rs532899532 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132883839 | AAGTTCTGTCTGGGC[A/G]AGGTGGCTCATGGCT | 55743 |
rs532980298 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132850333 | TCTTATAACGCCTAC[A/G]ACCACTTCACCAATG | 55743 |
rs533043622 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132857830 | CCAGAAGTTGGAAGG[C/T]TGTCACTCTTGAGTT | 55743 |
rs533118486 | snp | C/T | 1.64735e-05 | 0.00286993 | missense | CHFR | GRCh38.p7 | 12:132861536 | ACGACGAAAAGGACG[C/T]AGTCTTTCTGTCTGG | 55743 |
rs533181446 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132867092 | GCTCATCCAAAGGAG[A/C]CTCTGAAGAAGGAAG | 55743 |
rs533183283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132860996 | GACCTCAGATGATCC[A/G]TCCACCTTGGCCTCC | 55743 |
rs533209459 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132882502 | ATACTGCCATGAAAC[A/C/T]GGATATTAAAAATCT | 55743 |
rs533238568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132877303 | CTAGGTATGTAGTAG[A/G]CTACACCATCTAGGT | 55743 |
rs533249159 | snp | A/T | 0.031825 | 0.122064 | intron-variant | CHFR | GRCh38.p7 | 12:132866577 | TACAACACACCAGAA[A/T]GTTACAACACACCAG | 55743 |
rs533329369 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, downstream-variant-500B | CHFR, LOC101928530 | GRCh38.p7 | 12:132888747 | AGGCTGACCAAACGG[C/T]CTGTAGCATTAAGAT | 55743 |
rs533334808 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132855367 | GCGGAGGTTGCAATG[C/T]GCCAAGATTGTGCCA | 55743 |
rs533396646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132848786 | TCTCCAACACAATTC[A/G]TCAGCACCAGGCTCA | 55743 |
rs533411629 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132844307 | TTATTTTTATTGAGA[C/T]GGAGTCTCGCTCTGT | 55743 |
rs533416405 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | CHFR, LOC101928530 | GRCh38.p7 | 12:132888154 | CGGCGGCGTTCACGT[G/T]TGTGCTCCAGAGAAG | 55743 |
rs533441159 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132871974 | TGGTCCTAGGTTTTA[C/T]TCCCCATAACTCAAG | 55743 |
rs533445244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132859818 | AGGCTGAGGTGGGCA[A/G]ATCGCTTGAGCCCAG | 55743 |
rs533581400 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B | CHFR | GRCh38.p7 | 12:132840061 | ACCCCTGCACTAACA[C/T]GGGACCTCCCCTCTC | 55743 |
rs533686725 | in-del | -/GTT | | | intron-variant | CHFR | GRCh38.p7 | 12:132853184 | AGTATTAAGGTCAGG[-/GTT]GTTAATTCCCAGGAG | 55743 |
rs533823179 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132878446 | TGCACTCCAGCCTTG[C/G]CGACAGAGCTAGACT | 55743 |
rs533826266 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132849578 | CAACATGCTTGCCCC[A/C]AACTGCACATATTCA | 55743 |
rs533911569 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132877872 | CAGTGGCACCATCTC[A/G]GCTCACTGCAAGCTC | 55743 |
rs533963483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132882866 | ATGCACCACCACGCT[C/T]AGCTAATTTTTTAAG | 55743 |
rs534060095 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132865945 | TCCCAAAGTGCTGGG[A/T]TTACAGGCGTGAGCC | 55743 |
rs534061336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132855253 | TCTCGAAAAAAAAAA[A/G]AAAAGAAAAGAAAAA | 55743 |
rs534116903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132877379 | TGACACATTTCTCAG[A/G]CTGGATCCCTGTTGC | 55743 |
rs534189835 | in-del | -/ATAAATAAATAAATAAATAA | 0.00398564 | 0.0444627 | intron-variant | CHFR | GRCh38.p7 | 12:132885420 | TGTCTCAAAAAATAT[-/ATAAATAAATAAATAAATAA]ATAAATAAATAAATA | 55743 |
rs534200137 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132860494 | ACACCTTCCCCACAC[C/T]GATCAACCCCACGTG | 55743 |
rs534261361 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132866272 | ATCACATCAGAATGT[G/T]ACAACACACCAGAAT | 55743 |
rs534329329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132853946 | CGTTAAAAGCAGAGC[A/G]CGGTGGGCAACGTAC | 55743 |
rs534336743 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132873368 | TCCCCGTAAAACCTC[C/T]GAAACCAGGCAGTGG | 55743 |
rs534357480 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132887603 | GCTGTCAAGAGACAT[C/T]GCGGCTCCCTCAGCT | 55743 |
rs534368904 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132849665 | TAGTGGAGCAATCTC[A/G]GCTCACTGCAACCTC | 55743 |
rs534389499 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132853594 | AGGAAGCACAGGGCC[A/G]AGCTGTGTGCAGGCC | 55743 |
rs534497030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132843568 | CAAATAGACCCAGGG[C/T]CTAAAACAACCACAG | 55743 |
rs534515428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132858542 | CTAGCCTGGCCAACA[C/T]GGTGAAACCCTGTCT | 55743 |
rs534518887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132881578 | ATTGGCTGAAAATAC[C/T]GACCACGGGCCGGGC | 55743 |
rs534546612 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132869079 | GGGGAGTGACTGCTG[A/G]TGGGGCCGAGGGGAA | 55743 |
rs534562738 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132848907 | ATGGACTGTGATGGC[A/G]AGGAGTTGTATCCCT | 55743 |
rs534576173 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CHFR | GRCh38.p7 | 12:132864374 | TCTTACCACTTACAG[A/C]ATGTACCTGGCACAC | 55743 |
rs534638119 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132869888 | GCTCAAGCAGACACT[A/C]TAGGGATTGAAATGC | 55743 |
rs534721787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132842425 | CAAAATCCCTGTGAG[A/G]GAGGCGCCTTTCTCT | 55743 |
rs534792641 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132887529 | GCCCGCCGCAGCCCC[A/C]TCGCCAGCCGCGCTT | 55743 |
rs534885322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132870423 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 55743 |
rs535006652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132875459 | CCAGCCTGGCTAGCA[C/T]TGTGAAACCCCATCT | 55743 |
rs535014873 | snp | C/T | 0.00398564 | 0.0444627 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132840628 | AGGTGCCCCTCAGGC[C/T]CTGTAGGGTCTTGGA | 55743 |
rs535053119 | snp | A/G | 3.44839e-05 | 0.0041522 | intron-variant | CHFR | GRCh38.p7 | 12:132843978 | AGGCAGAAGCCAAGA[A/G]GCCAACCCAGACAGA | 55743 |
rs535072913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132880615 | GTGAGCCAAGATGGT[A/G]CCACTGCACTCCAGC | 55743 |
rs535073052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132874895 | TGCCCAGGACCAGCA[C/T]CCAGCGCGGGGAAGC | 55743 |
rs535106362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132847593 | GTGTGTCTGTGGCAA[A/G]CCTCAAGGCCCCACC | 55743 |
rs535128850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886723 | GCTATAAATTTCCCT[C/T]TGAGTACTGCCTTGG | 55743 |
rs535137488 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132843595 | ACAGCCCTGTATGGC[A/C]TGACGTCCTGCCGGC | 55743 |
rs535167933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132881605 | GGGCACGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 55743 |
rs535246412 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | CHFR | GRCh38.p7 | 12:132846424 | CCCGCCACCACGCCC[A/G]GCTAATTTTTTGTAT | 55743 |
rs535270687 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | CHFR | GRCh38.p7 | 12:132870079 | CCAGGCGTGCCGGGC[A/G]CGGTGGCTCATACCT | 55743 |
rs535298827 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132851830 | GCACAGCGAGGAGAG[A/G]TGCACCTGAGACAGC | 55743 |
rs535313174 | snp | G/T | 0.225597 | 0.248806 | missense | CHFR | GRCh38.p7 | 12:132857486 | CGGGACAGCGGCAGG[G/T]AGGACACAGGGACGA | 55743 |
rs535353587 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | CHFR | GRCh38.p7 | 12:132867033 | GCAAGACTCTGTCTC[-/A]AAAAAAACAGAAAAT | 55743 |
rs535381475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132863523 | AAAAACAAAGTAAAA[C/T]AAAACAAACAAACAA | 55743 |
rs535431002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132865133 | TGCTGCACTTGAAAC[A/G]CTGTGGGCCACGCTG | 55743 |
rs535509153 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | CHFR, LOC101928530 | GRCh38.p7 | 12:132889014 | CCTGGAGCGGCATCT[A/G]CATTAGAATGGCCAG | 55743 |
rs535546280 | in-del | -/A | 0.438246 | 0.16451 | intron-variant | CHFR | GRCh38.p7 | 12:132881257 | GCGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAG | 55743 |
rs535547829 | snp | A/C | 0.00358779 | 0.0422022 | upstream-variant-2KB, nc-transcript-variant | CHFR, LOC101928530 | GRCh38.p7 | 12:132888296 | TGCACTCATGAGGAG[A/C]CCCCAAGGGCGGTTT | 55743 |
rs535630556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132842453 | TCTGAGTCCACACAA[C/T]ATCTCGTCCTGAGGG | 55743 |
rs535660157 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | CHFR | GRCh38.p7 | 12:132859410 | GGCTGGAGTGCAGTG[C/G]CGCGATCTCGGCTCA | 55743 |
rs535733720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132865613 | CCTGACCTCAAGTGA[C/T]TCGCCTGTCTTGGCT | 55743 |
rs535761100 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132871167 | TTTAGGTATTTCAGG[A/G]GTGGCCAGGTGCAGT | 55743 |
rs535891608 | snp | A/C | 3.74616e-05 | 0.00432775 | intron-variant | CHFR | GRCh38.p7 | 12:132857579 | AAGTGCAAGAGGAAC[A/C]GTGTCCAGACAGTCC | 55743 |
rs535934253 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132882895 | AGTTTTTGTAGATAC[A/G]GGGTCTATGTTGCCC | 55743 |
rs535979777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132880921 | AGTGAGCCGAGATCA[C/T]GCCACTGCACTCCAG | 55743 |
rs536052892 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132874741 | GGGACCAGCACCCAG[C/T]GCGGGGAAGCCAGGC | 55743 |
rs536074141 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132847844 | GGAAGCGGCTCCTAC[A/G]AATTGGTGGCAGGAG | 55743 |
rs536115756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132874096 | TTCTCCCCTGGAGCC[C/T]CCAGAAGAAACCAGC | 55743 |
rs536151635 | snp | C/T | 0.000115638 | 0.00760302 | synonymous-codon | CHFR | GRCh38.p7 | 12:132847104 | CAACATGTTTTTCCA[C/T]GTCAAACCTCTGGTT | 55743 |
rs536174123 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132849288 | TGAACATTTACAGGC[A/G]TGATGCACTGCACCC | 55743 |
rs536186021 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CHFR | GRCh38.p7 | 12:132858154 | CTGAGTGCAGGAGTT[C/T]GAGACCAGCCTGGCT | 55743 |
rs536206980 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CHFR | GRCh38.p7 | 12:132846355 | GCAAGCTCCGCCTCC[C/T]GGGTTCACGCCATTC | 55743 |
rs536213481 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132852336 | AGAGAGGACAAGCCC[A/T]TAGAACCTATGATAT | 55743 |
rs536301533 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132863077 | AATTTTTTGTATTTT[C/T]AGTAGAGACAGGGTT | 55743 |
rs536305526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132841882 | GAGGCCGAGGCGGGC[A/G]GATCACTTGAGGTCA | 55743 |
rs536394655 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132863153 | CACCCACCTCGGCCT[C/T]CCAAAGTGCTGGGAT | 55743 |
rs536396076 | snp | C/T | 0.00301756 | 0.0387257 | synonymous-codon | CHFR | GRCh38.p7 | 12:132853435 | GCGCGGCTCACCTGT[C/T]GTCAGGCTGACGGAC | 55743 |
rs536424127 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132879562 | GGGCCAGTTAATTTT[C/T]GTATTTTTAGTAGAG | 55743 |
rs536448896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, missense | CHFR | GRCh38.p7 | 12:132862374 | AAGGTGGGAGGATCA[C/T]TTGATCCCAGGAGTT | 55743 |
rs536452144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132856051 | GCAATTTATACTATA[A/G]GACTTTATAGTCGCT | 55743 |
rs536644506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886854 | GAGTGTGGTGTTTCA[C/T]GTCCACATATCTGTG | 55743 |
rs536648644 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132879166 | TGCGCCACCATACCC[A/C]GCTAATTTTTTGTAT | 55743 |
rs536667604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132845583 | TGAGCCCAGGAGGTC[A/G]AGGCTGCAGTGAGCT | 55743 |
rs536672479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132853026 | GCCAACTCTGGTGAC[A/G]CAGGGCAGCTTCTGG | 55743 |
rs536715943 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132884146 | ATATCAGGCCGGGCA[C/T]AGTGGCTCACGCCTG | 55743 |
rs536797142 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132864338 | GCGCCCCGTGCTCAG[C/G]CAACGTGGAGAGGAG | 55743 |
rs536892691 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132880951 | GCCTGGGCGACAGAG[A/C]GAGACTCTGGCTCAA | 55743 |
rs536930794 | in-del | -/CTC | 0.00398564 | 0.0444627 | intron-variant | CHFR | GRCh38.p7 | 12:132876902 | CGGGTTCAAGTGATT[-/CTC]CTGTCTCAGCCTCCC | 55743 |
rs536978862 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132867325 | GGAATACACAGAGAG[A/C]CATAAAAACAAGGAG | 55743 |
rs536979458 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132874764 | AGCCAGGCCCTGGAA[C/G]AGGCGGGACTACCCA | 55743 |
rs537005682 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | CHFR | GRCh38.p7 | 12:132847945 | AGCTGGCTGCACCAG[G/T]GAGGAAACATGGCTC | 55743 |
rs537044284 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132880021 | TTCATACATTCAATG[A/C]AATTCCAGTCAAAAT | 55743 |
rs537062602 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132859781 | GTGCAATGGCTCACA[A/G]CTGTAATCCCAGCAC | 55743 |
rs537081193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132846839 | GAGCTGAGATCATGC[C/T]ACTGCACTCCAGTCT | 55743 |
rs537084515 | in-del | -/GA | | | intron-variant | CHFR | GRCh38.p7 | 12:132849482 | TCCCAGGAAAACAGT[-/GA]GAGACACAAAAGAAA | 55743 |
rs537209321 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132851787 | GACCCAGGGCAGAAA[C/G]ACAGCAGGTTAGAGA | 55743 |
rs537271543 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CHFR | GRCh38.p7 | 12:132857120 | CCCTCACGTGCCCGG[A/G]TGCTGGTGGAGGGAC | 55743 |
rs537275574 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132844288 | AGCCAATCTAGATAC[A/G]AATTTATTTTTATTG | 55743 |
rs537365941 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132863364 | AATACAAAATTGGCC[A/C/G]GGTGTGGTGGCACAT | 55743 |
rs537508825 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132879510 | ATTCTCCTGCCTCAG[A/C]CTCCTGAGTAGCTGG | 55743 |
rs537510682 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CHFR | GRCh38.p7 | 12:132862997 | TGCCTCCCTGGTTCA[A/C]GCCATTCTCCTGCCT | 55743 |
rs537545141 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132845018 | CTAAGTATGTCTTGA[A/G]AACCAAATTGCACAG | 55743 |
rs537547964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132885360 | AGCTTGCAGTGGGCC[A/G]AGATCGCGCCACTGC | 55743 |
rs537684016 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132864766 | GTGCTGGGATTACAG[C/G]CGTAAGCCACCACAC | 55743 |
rs537715809 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132883477 | ACGCCTCTAATCCCA[C/G]CACTTTGGGAGGCCG | 55743 |
rs537721825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132862972 | CGTGATCTTGGCTCA[C/T]TGCAAGCTCTGCCTC | 55743 |
rs537737331 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132856765 | CCTCACGTGCCCGGG[G/T]GCTGGTGGAGGGACT | 55743 |
rs537762517 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132882503 | TACTGCCATGAAACC[A/G]GATATTAAAAATCTT | 55743 |
rs537785299 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132852121 | CCGAGTAGCTGGGAC[-/T]TACAGGTGCCTGCCA | 55743 |
rs537786958 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132868308 | ATCCTGGCTAACACG[G/T]TGAAACTCCGTCTCT | 55743 |
rs537885478 | snp | G/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132858633 | CTCAGGAAGCTGAGG[G/T]AGGAGAATCGTCTGA | 55743 |
rs537978939 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132872849 | CTGGGCAGAAGCGGA[A/C]TAAATGCTGGGCCGT | 55743 |
rs537998604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132866697 | AGGAATGTTACAACA[C/T]ACCAGAATGTTACAA | 55743 |
rs538056072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132866403 | AATGTTACAACAGAC[C/T]GGAACACCACACCGG | 55743 |
rs538059968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132872211 | AAGGGATGTAGCCAG[A/G]AGGAACGTTCAGAGA | 55743 |
rs538134942 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132844556 | CCCAAAGTGCTGGGA[C/T]TACAGGCGTGAGCCA | 55743 |
rs538136772 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132860263 | AAGGTAGAGAAAAAC[C/T]CTGTCCTGAGACACC | 55743 |
rs538257993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132855304 | GTGCATGCCTGTAAT[C/T]CCAGCTATTTGGGAG | 55743 |
rs538323273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132868392 | CTACTCAGAGGCTGA[A/G]GCAGGAAAATGGCGT | 55743 |
rs538323737 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132861159 | AGTGTTAGGATTACG[G/T]ATATGAACTACTGCA | 55743 |
rs538384274 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CHFR | GRCh38.p7 | 12:132873959 | CGCTCCGACCACACA[A/G]CCCTGCTTATGCTCA | 55743 |
rs538499840 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132879104 | CCACCTCCCAGGTTC[A/C]AGCCATTCTCCTGCC | 55743 |
rs538555507 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132884107 | CCTGGGTGACAGAGT[A/C]AGACTCCGTCTCAAA | 55743 |
rs538564215 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132877461 | AAAGACAGCATTTCT[C/T]CTCCTCCTCAGCCGT | 55743 |
rs538617274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132851239 | CAGAAGATCCACCTA[C/T]CTTGGCCTCCCAAAG | 55743 |
rs538645880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132883587 | AAAAAATTAGCCGGG[C/T]ATGGTGGCGGGTGCC | 55743 |
rs538708822 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132879401 | TTTTTTTTTCTTTTT[C/T]TTTTTTTGAGACGGA | 55743 |
rs538725203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132855995 | CTTGGCCTGGTGATG[A/G]TGCCTCTTCTGTAAT | 55743 |
rs538772766 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132860685 | CTTCTCCCTAAATCA[C/T]CTTCAATGTGAAGAT | 55743 |
rs538873969 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132840712 | CCTGGGCTTGGGGCC[A/G]TGGTCACTCACACAA | 55743 |
rs538884451 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132878222 | ATACTTGTAAACCCA[C/G]CACTTTGAGAAGCTG | 55743 |
rs538932607 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132872767 | CACAGTTCTGTTCCT[G/T]GCAGCCATCACAACC | 55743 |
rs538975143 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132844974 | AAAACTCCCAAAAAA[C/G]AAGAAGAAAATGAGA | 55743 |
rs538986821 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132883077 | TTTGCTGCGCTTGAC[C/G]CTTGGTGGGTTAAAT | 55743 |
rs539157069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132849995 | GTCTTGCTCTGTCAC[C/T]CAGGCTGGAGTGCAC | 55743 |
rs539169091 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CHFR | GRCh38.p7 | 12:132889542 | CTAAGCTAAGCCATC[A/G]CATCCCCTGTGACCT | 55743 |
rs539351007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132872228 | GGAACGTTCAGAGAG[C/T]GCCCTCACGTGCACC | 55743 |
rs539433109 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132877834 | TTGAGACGGAGTCTC[A/G]CTCTGTCGCCCAGGC | 55743 |
rs539510794 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132882701 | TCTCCATGCCAGAAC[A/G]TCAGGTTTTTTTTTT | 55743 |
rs539548289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132882175 | GTAAACTAACAAGCC[A/G]TGGTGCATCCAAACC | 55743 |
rs539580069 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132849486 | AGGAAAACAGTGAGA[C/G]ACACAAAAGAAAGAA | 55743 |
rs539625713 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132881470 | AGAAGAGATATGGAT[A/G]GCAAATTAAGCACAT | 55743 |
rs539637783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132876109 | GGAACCTGGGAGTCG[A/G]AGGTCGCAGTGAGCC | 55743 |
rs539642686 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132854675 | GCCGGGCATGGTATC[A/G]GGAGCCTGTAGTCCC | 55743 |
rs539660104 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | CHFR | GRCh38.p7 | 12:132845194 | GGCACGGTGGCTCGC[A/G]CCTGTAATCCCAGCA | 55743 |
rs539699827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132880930 | AGATCACGCCACTGC[A/G]CTCCAGCCTGGGCGA | 55743 |
rs539790786 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | CHFR | GRCh38.p7 | 12:132859463 | TCATGCCATTCTCCT[A/T]CCTCAGCCTCCTGAG | 55743 |
rs539853053 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132875941 | GCACTTTGGGAGGCT[A/G]AGGCAGGCAGATCAC | 55743 |
rs540011822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132843340 | CAGAGGCAGGAGAAT[C/T]GCTTGAACCTGGGAG | 55743 |
rs540035306 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132879067 | TGGAGTGCAGTGGCA[C/T]CATCTCGGCTCACCA | 55743 |
rs540234135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132860855 | CCTGCCGGGTTCAAG[C/T]AATTCTCCTGCCTCA | 55743 |
rs540365836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132871859 | CCACAAAACAAAAAC[A/G]GGACTTCTGGAGCTG | 55743 |
rs540426488 | snp | C/T | 1.68119e-05 | 0.00289926 | missense | CHFR | GRCh38.p7 | 12:132877628 | CTCCAGAGACCAGTT[C/T]ATTGCTGGGGAAGGA | 55743 |
rs540522996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132864717 | TGGTCTTGAACTCCC[A/G]ACCTCAGGCGATCCA | 55743 |
rs540538401 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132876207 | AAGAAAAAAGCTGAC[A/G]CTACAACAGTATGTG | 55743 |
rs540583915 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132870132 | CTGAGGCGGGTAGAT[C/G]ACGAGGTCAGGAGAT | 55743 |
rs540605749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132853070 | GCTGGGGAGAAGCCC[A/G]CCTCTTACTTGAGGG | 55743 |
rs540624001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132875650 | AAAAAGGAATAGGCA[C/T]ATTCTGAGTAACACT | 55743 |
rs540633771 | in-del | -/ATAAA | | | intron-variant | CHFR | GRCh38.p7 | 12:132845085 | AACATCAAAATTAAA[-/ATAAA]TACAACAAAAGTGAA | 55743 |
rs540698247 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CHFR | GRCh38.p7 | 12:132859579 | ATGGTCTCAATCTCC[C/T]GACCTCGTGATCCAC | 55743 |
rs540750625 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132880428 | TTGGGAGGCCAAGGG[C/G]GGGGCGGATCACAAG | 55743 |
rs540759128 | snp | A/G | 1.64985e-05 | 0.0028721 | missense | CHFR | GRCh38.p7 | 12:132859186 | GGGCATTTCTACGCG[A/G]TTGTGCGACCAACAA | 55743 |
rs540812591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132865294 | GGAAGATACGATGAA[A/G]GGTACACAGCCCAAG | 55743 |
rs540832390 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132852520 | CACAGGAAAGACCCT[C/G]CGAGGTCAACATGCC | 55743 |
rs540867084 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132847574 | CTGAGCGGGCGCCTG[C/T]CAGGTGTGTCTGTGG | 55743 |
rs540931944 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132885191 | GAGGCAGGCAGATCA[C/T]GAGGTCAGGAGATTG | 55743 |
rs540956889 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132857337 | GGGTGGATGCCCTCA[C/G]GTGCCTGGGTGGTGG | 55743 |
rs541037549 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CHFR | GRCh38.p7 | 12:132842580 | GGGCAATGCAGATGG[C/T]GCTGTGAACCTCCTT | 55743 |
rs541056471 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132863437 | CTTGAACCCAGGAGG[C/T]GGAGTTGCAGCGAAC | 55743 |
rs541100767 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CHFR | GRCh38.p7 | 12:132847954 | CACCAGTGAGGAAAC[A/G]TGGCTCCCGGCTCCC | 55743 |
rs541119748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132868560 | TTGCAGGCACCTGTA[A/G]TCCCAGCTACTCGGG | 55743 |
rs541179525 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132841365 | GCGGGCTGCGGCCCC[C/T]GGGGCTCTGGGGAGG | 55743 |
rs541187851 | in-del | -/A | 0.00358779 | 0.0422022 | intron-variant | CHFR | GRCh38.p7 | 12:132854215 | ATTTTTTTCATAAGG[-/A]AAAAAATGTAAATGA | 55743 |
rs541241838 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132840882 | CTAACTTGGCGGCCA[C/T]GTCGAGGGTTAGCAG | 55743 |
rs541303770 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132861228 | TTCAGAATGCACTAT[C/T]TCCAGACCAAGAGAA | 55743 |
rs541315009 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | CHFR | GRCh38.p7 | 12:132856101 | ATGTGCTCATGTGGG[-/A]AAAAAATAACATGGA | 55743 |
rs541339986 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132845922 | AACAGTATGAACCTG[C/T]GATCAATTTAGCAGC | 55743 |
rs541345009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132864061 | GAATAAGGATTACAG[A/G]TGTGAATAAGGATTA | 55743 |
rs541385187 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CHFR | GRCh38.p7 | 12:132884482 | TTCTACAACTGTTAG[A/G]AACTGAATGTTTGTA | 55743 |
rs541404735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132869309 | CGTGTCAATGAGTGG[C/T]GATGGTCCCACACCT | 55743 |
rs541551043 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | CHFR | GRCh38.p7 | 12:132874366 | GCCCAGGACCAGCAT[G/T]CAGCGCAAGGAAGCC | 55743 |
rs541618077 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132842666 | TGCCTGCTCACGGGA[C/T]GGACGAGAACCCAGC | 55743 |
rs541641258 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132880781 | ACCAGCCTGACCAAC[A/G]TGGTGAAACCCAGTC | 55743 |
rs541643632 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CHFR | GRCh38.p7 | 12:132848009 | CAGATAAACACCAAT[A/G]GAATGCAGAGAACCA | 55743 |
rs541702051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132853284 | GCAACCAACTGTGAG[C/T]GCAGGGAGACCAATG | 55743 |
rs541715629 | snp | A/G | | | missense, intron-variant | CHFR | GRCh38.p7 | 12:132869660 | GCAGGAGAAGGCTCC[A/G]TGGAAGAGGCCGAGG | 55743 |
rs541767109 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132852645 | GGAAGGAGCTTGTCC[A/C]GTGACCCAGACAGAG | 55743 |
rs541902910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132843207 | GCCTCTGGTCCCTCC[A/G]TAACTAGTTTCCTCG | 55743 |
rs541915007 | in-del | -/AAAC | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132885421 | TCTCAAAAAATATAT[-/AAAC]AAATAAATAAATAAA | 55743 |
rs541929266 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132881041 | GGTGGCCAAGGCGGG[A/C]GGATCACTTCAGACC | 55743 |
rs542153503 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132841436 | AGAGCACCTGTCGGA[C/G]ACCCTGCGTCCCTTC | 55743 |
rs542180166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132879678 | ACAGGCGTGAGCCAC[C/T]AGCGCCCGGCCCTGA | 55743 |
rs542188772 | snp | A/G/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132885782 | GCGCAGAAAGATGTC[A/G/T]TTAGCCCAGAGTAAT | 55743 |
rs542220281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132864392 | GTACCTGGCACACTG[C/T]CTCACATTTAGTAGC | 55743 |
rs542403204 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132856920 | GACCGCCCTCACTTG[C/T]CTGGGTGCTGGTGGA | 55743 |
rs542436315 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CHFR | GRCh38.p7 | 12:132868604 | AGAATGGCGTGAACC[C/T]GGGAGGCGGAGCTTG | 55743 |
rs542441258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132841933 | CCAACATGGTAAAAC[C/T]CCATCTCTACTAAAA | 55743 |
rs542467983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132880244 | CTAAAACTATGAAAC[C/T]TCCAGTGGAAAAGAC | 55743 |
rs542468260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132862677 | CTCCGCCTCCTGGGT[C/T]GACGCCATTCTCCTG | 55743 |
rs542547306 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132873569 | GGCTGGAGTGCACAC[A/G]GACTTGGGTGCATGC | 55743 |
rs542602264 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132846450 | TGTATTTTTCTTTTT[C/T]TAGTAGAGACAGGGT | 55743 |
rs542627650 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132846091 | TTGTCTTTTTGTTTT[C/T]ATTTCTACGTTTGTC | 55743 |
rs542665576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132851846 | TGCACCTGAGACAGC[C/T]GGGGAAGAAGCAGAC | 55743 |
rs542673371 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | CHFR | GRCh38.p7 | 12:132840334 | GGCAGCCCCAGACAC[A/G]AGCCCAACACGAGAG | 55743 |
rs542688277 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132845389 | GTTGAACCTGGGAGG[C/T]GGAGCTTGCAGGGAG | 55743 |
rs542691026 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CHFR | GRCh38.p7 | 12:132857278 | CCACCCTCACGTGCC[C/T]GGGTGCTGGTGGAGG | 55743 |
rs542702171 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132863674 | CAGCACAGTGACTTG[C/T]AGGGAGAGCGCTATC | 55743 |
rs542716211 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | CHFR | GRCh38.p7 | 12:132878605 | CGGGCAGATCACAAG[C/G]TCAGGAGATCGAGAC | 55743 |
rs542754125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132850589 | ACGGCCATGTGTCCC[A/G]ACGCTGCAGGCTAGG | 55743 |
rs542792789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132858962 | ACCTCAGCAGATGCC[A/G]GGCCAAACAGGACCT | 55743 |
rs542817381 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132850283 | TAATGTTAGGTAAAC[A/C]CTCGCTAAAATTCTC | 55743 |
rs542836961 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132881794 | AATGGCTTGAACCCG[A/G]GAGGCGGAGGTTGCA | 55743 |
rs542881364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132862141 | TTAGACAGGCGTGGT[A/G]GCGAGTGCATGTAGT | 55743 |
rs542882636 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | CHFR | GRCh38.p7 | 12:132857145 | AGGGACAGCCCTCAC[A/G]TGCCCGGGTGCTGCT | 55743 |
rs542944789 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132867700 | CTCTTCTGTTCATAG[G/T]AATCTGCAGACTGCT | 55743 |
rs542960582 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132855040 | TGAGGTCAGGATTTC[A/G]AGACCAGTCTGGCCA | 55743 |
rs543048125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886391 | AAAAAAAAAAAAAAA[C/T]TGCTTCCAAACAGCA | 55743 |
rs543054656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132879777 | AATATCTCATCATTA[A/G]TCATTACTGCCTATA | 55743 |
rs543199843 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132883276 | CTACAAAATACAAAA[A/G]TTAGCCAAGCATGGT | 55743 |
rs543239273 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132863856 | CTCTGCCTCCTGGGC[C/T]AAAGCGATCCTTCCA | 55743 |
rs543261903 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CHFR | GRCh38.p7 | 12:132857296 | GTGCTGGTGGAGGGA[C/T]AGCCCTCACGTGCCC | 55743 |
rs543277570 | in-del | -/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132844452 | CCACACCGGGCTAAT[-/G]TTTTTGTATTTTTAG | 55743 |
rs543287060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132881797 | GGCTTGAACCCGGGA[A/G]GCGGAGGTTGCAGTG | 55743 |
rs543340281 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132862682 | CCTCCTGGGTTGACG[C/T]CATTCTCCTGCCTCA | 55743 |
rs543404161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132842019 | GGAGGCTGAGGCAAA[A/G]GAATTGCTTGAACCT | 55743 |
rs543489645 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132852446 | GTGCACAAGACCAAT[C/T]GATGTGGCAGCAGAA | 55743 |
rs543506724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132873731 | CCACAGGGCTGGCTA[C/T]GGGGCTAGAGTGTGC | 55743 |
rs543507917 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132840837 | CCCCAGGCTCGGGGC[C/T]GCGGTCACTCACCGG | 55743 |
rs543547155 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CHFR | GRCh38.p7 | 12:132876763 | ATACCTTGGGAGCCT[A/G]ATTAACTACAGTCAT | 55743 |
rs543551307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132857651 | CCCACCACGGAAGGG[C/T]CTACAGGGGCCCAGC | 55743 |
rs543570180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132879256 | CGCCTCAGCCTCCCA[A/G]AGTGTTGGGATTACA | 55743 |
rs543659613 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | CHFR | GRCh38.p7 | 12:132855273 | GAAAAGAAAAAAAAA[A/T]TAGCCAAGTTTGGTG | 55743 |
rs543667123 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132856989 | CACCCTCACGTGCCC[A/G]GGTGCTGGTGTGGAT | 55743 |
rs543752956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132850327 | CTTAAGTCTTATAAC[A/G]CCTACGACCACTTCA | 55743 |
rs543810326 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132856130 | GAATGATGTCCCTCT[G/T]TCACAGCCAGAGATG | 55743 |
rs543915355 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132873109 | CACAAAACGGCAACC[A/G]GGCAAAACGACTGAA | 55743 |
rs543975799 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132878686 | TAGCCGGGCGTGGTG[C/G]CGGGCGCCTTGTAAT | 55743 |
rs544062680 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132883829 | TAAAATAATCAAGTT[A/C]TGTCTGGGCGAGGTG | 55743 |
rs544205773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132855537 | CTGGGTGTGGTGGCA[C/T]GCGCCTGTAGTCCCA | 55743 |
rs544229388 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CHFR | GRCh38.p7 | 12:132889203 | GCTGAGGTGGGCAGA[G/T]TCCTTGAGCCCGGGA | 55743 |
rs544311918 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CHFR | GRCh38.p7 | 12:132881825 | GTGAGCTGAGATTGC[A/G]CCACTGCAAATCCAG | 55743 |
rs544357554 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132867015 | CTCCAGCCTGGGCAA[C/G]AGAGCAAGACTCTGT | 55743 |
rs544361669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132854846 | TTTGTTTCTCACGCC[C/T]ATAATCCCAGCACTT | 55743 |
rs544414978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132866553 | GATGTTACAACACAC[C/T]GCGATTGTTACAACA | 55743 |
rs544473558 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132866001 | CATCTTGAAGTGTTA[G/T]TTTCTTTCACTCATA | 55743 |
rs544515173 | snp | A/C/G | 0.000339542 | 0.0130259 | intron-variant | CHFR | GRCh38.p7 | 12:132877692 | ACACGGGATATGATC[A/C/G]TGGTAACTGTGAACA | 55743 |
rs544575403 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132844242 | AAATGGGGTGAAGAC[A/C]ACGGGCGACACATTA | 55743 |
rs544587148 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132882432 | CTGGTGAGTACATTT[C/T]CCAAAACTCATGGAA | 55743 |
rs544598672 | in-del | -/TGTAGCCAGGAGGAACGTTCCTATGGGAAGGGA | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132872169 | GAGCAAGAAATGGGG[lengthTooLong]TGTAGCCAGGAGGAA | 55743 |
rs544640419 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132843805 | ACACAAAAAATTAGC[C/T]GGGCGTGGTGGCGGG | 55743 |
rs544693001 | in-del | -/AA | | | intron-variant | CHFR | GRCh38.p7 | 12:132875029 | GCCAGGCCCTGATGT[-/AA]AGGCAGGAAAGCCCA | 55743 |
rs544703917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132849128 | ATTTATTTTTTATTT[C/T]TGTAGAGACAGGGTC | 55743 |
rs544721895 | in-del | -/CT | 0.244776 | 0.249945 | intron-variant | CHFR | GRCh38.p7 | 12:132844460 | GGCTAATTTTTTGTA[-/CT]TTTTTAGTAGAGACT | 55743 |
rs544740314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132854316 | TAGGTGCACCCTTTC[C/T]GATCGGTGTCTGGAT | 55743 |
rs544797090 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132859796 | ACTGTAATCCCAGCA[A/C]TTTGGGAGGCTGAGG | 55743 |
rs544837794 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132853003 | GACGGGGAAACATTT[C/T]GCATTAAGCCAACTC | 55743 |
rs544865208 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132867531 | CCACTGTGAAACCTC[C/G]AGGCAAAAACCTGAG | 55743 |
rs544877540 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132857733 | TCAGAGGCCACACGG[A/C]CTCTGTGTTTTCAGG | 55743 |
rs544993812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132850826 | TCACCTAACACTTTC[A/G]CATATAAGAAGCTCT | 55743 |
rs544996948 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132862194 | GCAGAAAAATTGCTT[A/G]AACCCGGGAGGCGGA | 55743 |
rs545089854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132880411 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGCCAAGG | 55743 |
rs545093760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132856267 | CCGCTAAGTGTTCAC[C/T]CAGTCCCTGCCACGC | 55743 |
rs545149319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132862000 | GCTTTGGGCCGGGTG[C/T]GGTGGCTCACACCCG | 55743 |
rs545149620 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132850144 | AATTTTAGTAGAGAT[A/G]GGATTTCACCATGTT | 55743 |
rs545238202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132867112 | GAAGAAGGAAGGAGC[A/G]GATGCAACAAGGCCT | 55743 |
rs545256249 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132855186 | GATGAATGTTGCAGT[A/G]GGCGAAGGTCATGCC | 55743 |
rs545264857 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132860716 | TTAAGCTACATTTTT[A/G]GAAATTATTGTCCTA | 55743 |
rs545292237 | snp | C/T | | | upstream-variant-2KB, intron-variant | CHFR, LOC101928530 | GRCh38.p7 | 12:132888105 | TGTTCTGAACGCGCG[C/T]AACTTTTGCCTCAGT | 55743 |
rs545303448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132872516 | TACTCATAGGAACAG[C/T]GTAAATACGTAACGA | 55743 |
rs545310763 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | CHFR | GRCh38.p7 | 12:132840273 | AGCAGTGAGGCACTC[A/G]GAGCTCACTCTGCAT | 55743 |
rs545324804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132859822 | TGAGGTGGGCAGATC[A/G]CTTGAGCCCAGGAGT | 55743 |
rs545324835 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132866420 | GAACACCACACCGGA[A/T]TGTTACAACACACCC | 55743 |
rs545381751 | in-del | -/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132862598 | CAGAGCAAGACCTCA[-/T]TTTTTTTTTTGAGAC | 55743 |
rs545421960 | in-del | -/TT | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132885908 | TTCAAATACTTCCTC[-/TT]GTCTTAAAGGGATAA | 55743 |
rs545432113 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CHFR | GRCh38.p7 | 12:132844618 | GCAAAACAATCCCAC[A/G]TGGATATAACATTTA | 55743 |
rs545473860 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132871744 | GCCATTACACTTCAG[C/T]CTGGGCAACAAGAGC | 55743 |
rs545522054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132849699 | CTCCTGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 55743 |
rs545523118 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132862075 | GTCAGGAGGTCGAGA[C/T]CAGCCTGGCCAACAT | 55743 |
rs545585269 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132854964 | ACAAAATTAGCGGCC[A/G]GGCGCGGTGGCTCAC | 55743 |
rs545702707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132848949 | AGGCTCACATTTTCT[A/G]GTTTGTTATTTTTTA | 55743 |
rs545741374 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132852038 | GCTCAGGCTGGACTG[C/T]AGTGGCGTGATCTCG | 55743 |
rs545837095 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132871351 | CAGCTACCTGGAAGG[C/T]TGAGGCAGGAGAATC | 55743 |
rs545900025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132877078 | GGGATTACAGGTGTG[A/G]GCCACCGCGCCCGGG | 55743 |
rs546055046 | snp | A/G | 0.000101204 | 0.0071128 | synonymous-codon | CHFR | GRCh38.p7 | 12:132848681 | GCAGCCGGTCCGGGT[A/G]CAGCCCCAGTACAGG | 55743 |
rs546118391 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132853746 | GTGTTAGAGAGGGAC[C/T]AGAACGAGTCGAAGG | 55743 |
rs546136386 | snp | C/G | 0.000798403 | 0.0199641 | missense, intron-variant | CHFR | GRCh38.p7 | 12:132869663 | GGAGAAGGCTCCGTG[C/G]AAGAGGCCGAGGCTG | 55743 |
rs546197054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132854484 | CAATTCAAACGCTGG[A/G]GACATTACCGAGCTG | 55743 |
rs546206649 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132870006 | CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGACC | 55743 |
rs546228427 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132850422 | AAAGCTGGGCCGAGC[C/T]GCCATCTGCTGACCA | 55743 |
rs546349675 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132864540 | GTCACCCAGGCTGGA[C/G]TGCAGTGGCAGGATA | 55743 |
rs546357534 | in-del | -/A | 0.273049 | 0.248935 | intron-variant | CHFR | GRCh38.p7 | 12:132878833 | CAAAAAAAAAAAAAG[-/A]AAAAAAAAAAACTCA | 55743 |
rs546413580 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132866135 | ATGGGTTTGGTCTCC[A/G]CTGTTCCTCTTATCT | 55743 |
rs546432695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132875559 | ACCCGGGTGGCGGAG[A/G]TTGCAGTGAGCCGAG | 55743 |
rs546447426 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132875662 | GCACATTCTGAGTAA[A/C]ACTGACACAGACTTC | 55743 |
rs546510676 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132873507 | GAATCCCACACATAT[A/G]CTGGACTGACTTTCT | 55743 |
rs546528841 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, downstream-variant-500B | CHFR, LOC101928530 | GRCh38.p7 | 12:132888987 | ACCATCTATTCTCTC[C/T]GAAGCCTGCTGCCTG | 55743 |
rs546532214 | in-del | -/CAAAAAAACAAA | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886310 | GCAAGACTCTTATCT[-/CAAAAAAACAAA]CAAAAAAACAAAAAA | 55743 |
rs546708406 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132859360 | AATACATGCAGTCTT[A/T]TTTTTTTCGAGACAG | 55743 |
rs546832718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886761 | CTAAATACCTTTTGG[C/T]GTATTCTATTTTTGT | 55743 |
rs546878701 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132871128 | TAAGACATATTTGCC[C/G]CATTCTCCCTCACCA | 55743 |
rs546938165 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132876663 | ATTTCTGAGACATAC[A/T]TAATTTGAATACATT | 55743 |
rs546940103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132870450 | GCAGGAGAATCTCTC[A/G]AACCCGGCAGGAGGA | 55743 |
rs546979299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132842856 | ACTGCATGAAACGAA[A/G]GGATAAAGGAAGAGC | 55743 |
rs547002043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132875877 | GCTCCATAAAACACC[A/G]TAAGTGAAAAAAGCT | 55743 |
rs547083252 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132850749 | CAGGGCTCAGTGCAC[A/C]GAGCAACACCGGTGT | 55743 |
rs547086677 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132887284 | CAGGAGCCGTCCCCA[A/G]GGCTGCGGCGGCGGC | 55743 |
rs547175696 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132879840 | GACAAAAAAGCGAAG[C/G]GTTTGGTCAGGAGAC | 55743 |
rs547207924 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132868431 | GAGAATGGCGTGGGA[A/G]GCGGAGCTTGCAGTG | 55743 |
rs547224191 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132852991 | AAAAAGGCACCTGAC[A/G]GGGAAACATTTCGCA | 55743 |
rs547257437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132851951 | ATGATCTTTGATTTA[A/G]CAGCTGGAGCAAGAT | 55743 |
rs547285650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132858019 | GGGGTCTACAGCCTC[C/T]GGCTCTGGGTTCCAG | 55743 |
rs547342987 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | CHFR | GRCh38.p7 | 12:132846301 | GGAGTCTCGCTCTGT[C/G]CCCCAGGCTGGAGTG | 55743 |
rs547347915 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132866983 | AGGTTGCAGTGAGCC[A/G]AGATTGCGCCACTGC | 55743 |
rs547367271 | snp | C/G | 0.000745742 | 0.0192967 | synonymous-codon, intron-variant | CHFR | GRCh38.p7 | 12:132869761 | CGACGGAGGGACCCG[C/G]GGATCGGCCCCTCGC | 55743 |
rs547377537 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132884236 | CCAGCCTGACGAACA[C/T]GGAGAAACCCCGTCT | 55743 |
rs547378868 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132881850 | ATCCAGCCTGGCGAC[A/G]GGGCAAGACGCTGTC | 55743 |
rs547438484 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CHFR | GRCh38.p7 | 12:132862805 | CAGGATGGTCTCGAT[C/T]TCCTGACCTCATGAT | 55743 |
rs547594947 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132885830 | ACCCACATAATTTGT[C/T]TCTAGGGCCTCTGCT | 55743 |
rs547619077 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132841267 | CAAAACTGCCCCTCT[C/T]GGCGGGACGGCCGCA | 55743 |
rs547640410 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132844813 | TGTTTATACTTTTTT[A/G]GTAGAGATGGGGTTT | 55743 |
rs547701046 | in-del | -/CTCCACCCA | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132858900 | AGTGGGCTGAGAAAG[-/CTCCACCCA]CTCCACCCACTCCAC | 55743 |
rs547712957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132873190 | ACAGAACTCACATCC[A/G]AGTGACCACCACGGT | 55743 |
rs547873870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132858187 | TATGGTGAAACTCCC[A/G]TCTCTACTAAAAATA | 55743 |
rs547884588 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | CHFR | GRCh38.p7 | 12:132868262 | TTTGGGAGGCCGATC[C/G]GACAGATCACGAGGT | 55743 |
rs547902011 | snp | A/G | 0.000192623 | 0.00981194 | synonymous-codon, intron-variant | CHFR | GRCh38.p7 | 12:132869809 | GGTATCTTTGGTCCC[A/G]TGGAACACATTTTCC | 55743 |
rs547935291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132864327 | CATCATCTCCAGCGC[C/T]CCGTGCTCAGCCAAC | 55743 |
rs548023995 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132874742 | GGACCAGCACCCAGC[A/G]CGGGGAAGCCAGGCC | 55743 |
rs548109082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132845419 | GCTGAGATTGTGCCA[C/T]TGCACTCCAGCCTGG | 55743 |
rs548126333 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132846795 | TGATGCAGGAGAATC[A/G]CTTGAACCCAGGAGG | 55743 |
rs548167667 | snp | A/G | | | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886861 | GTGTTTCATGTCCAC[A/G]TATCTGTGAATTTTC | 55743 |
rs548193657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132879891 | TTCCTAAACGTTCCA[C/T]ACAGAAAGACACCCT | 55743 |
rs548246175 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886047 | TCAGACACAGTGGTT[C/T]ACACCTGTAATCCCA | 55743 |
rs548271006 | snp | A/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132866613 | TACAACACACCAGAA[A/T]GTTACAACACACCGC | 55743 |
rs548347593 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132875283 | CAAAAAAAATCCTGC[A/T]GTGAGAACAGCACAC | 55743 |
rs548385992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132842342 | CAACAGTGAAATCTC[C/T]TTTTGTAACAACATG | 55743 |
rs548491570 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132862895 | AAGACCTCATTTCTT[C/T]TGTTTTCTTTTTCTT | 55743 |
rs548637911 | snp | A/G | 0.000267268 | 0.0115569 | intron-variant | CHFR | GRCh38.p7 | 12:132857387 | TGCCCGGGTGCTGGT[A/G]TGGATGCCCTCACTT | 55743 |
rs548921231 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132873802 | CAGATGCCGAGGGGC[A/G]ACTGCAGCCATCACT | 55743 |
rs548922117 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132840961 | TATTCTTTCAAATAC[C/T]ATACTATACCCAATT | 55743 |
rs548946821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132879332 | ATAAGAAACTGCATC[C/T]TATATACAGGGATGC | 55743 |
rs548980628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132873369 | CCCCGTAAAACCTCC[A/G]AAACCAGGCAGTGGC | 55743 |
rs549027841 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132872616 | CTAACCAGCCACTAC[A/G]CCTCCTCACGTGCTT | 55743 |
rs549054300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132842921 | ATGCAACCTGAGAGA[A/G]GCATAATGACCATAT | 55743 |
rs549085505 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CHFR | GRCh38.p7 | 12:132872192 | GGAGGAACGTTCCTA[C/T]GGGAAGGGATGTAGC | 55743 |
rs549106804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132844924 | AGGCGTGAGCCTCCA[C/T]GCCCGGCCCCACATG | 55743 |
rs549120489 | snp | A/G | | | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132840507 | TCAGTTTACAAACAA[A/G]GATAACAGGTGATTT | 55743 |
rs549150480 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | CHFR | GRCh38.p7 | 12:132877769 | CCATTGTACATATGT[A/T]AAAAAAAACACTTGA | 55743 |
rs549207239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132850411 | ATTCCTGGGGAAAAG[C/T]TGGGCCGAGCTGCCA | 55743 |
rs549211800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132877431 | GTTATAAAAATGAGC[C/T]GCTGTTATCACACTA | 55743 |
rs549268530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132855788 | AGTGGTTTTGGTTTC[C/T]TTCTTTTTGCTTAAC | 55743 |
rs549268961 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132858576 | CTAAAAAATACAAAA[A/C]AATTAGCCGGGCATG | 55743 |
rs549415294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132866654 | ATGTTACAACACACC[A/G]GAATGTTACAACACA | 55743 |
rs549524419 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132884859 | TGAGAGGCCGAGGCA[A/G]ACAGATTGCTGGAGC | 55743 |
rs549612143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132884083 | GAAGATCGCACCACT[A/G]CACTCCAGCCTGGGT | 55743 |
rs549614443 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132879380 | GTAATTCTGACACTT[G/T]GGGATTTTTTTTTTC | 55743 |
rs549634294 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132843937 | CTGGGCAAAAACAGC[A/G]AAACTGTCTCAAAAA | 55743 |
rs549697602 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132856242 | CTCTGCTGGCTACCC[C/T]CTGGCTACCCCGCTA | 55743 |
rs549730075 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | CHFR | GRCh38.p7 | 12:132874552 | AGCCAGGCCCCGGAA[C/T]AGGCGGGACTGCCCA | 55743 |
rs549748047 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132844656 | TATTTTTTGAGACCA[A/G]GTCTTGCTCTGTCGC | 55743 |
rs549757086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132862250 | ACTGCACTCCAGCCT[A/G]GGCAACAAGAGCGAA | 55743 |
rs549772492 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132851029 | AGGATTTCCCTCTGT[C/T]GCCAAGGCTGGAGTA | 55743 |
rs549782692 | snp | A/G | 1.64798e-05 | 0.00287047 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132841507 | GTATTTTAAAAACAC[A/G]CTCTCTTCACCTCCA | 55743 |
rs549816985 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132867745 | CGCGAGAGCCAAGCA[C/T]TCCAGGACTAAGAAT | 55743 |
rs549817234 | snp | A/T | 1.83883e-05 | 0.00303213 | intron-variant | CHFR | GRCh38.p7 | 12:132861667 | CAAGATAGGTGCTGA[A/T]CCATCCAGCTCAGGA | 55743 |
rs549826875 | snp | C/T | 0.000164821 | 0.00907652 | missense | CHFR | GRCh38.p7 | 12:132841588 | TGTTCACAGATATGA[C/T]TGAATTTCCTGCAGG | 55743 |
rs549878515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132867235 | AAACAGGCCCAGAGA[A/G]CGTGAGAGGTTTCTG | 55743 |
rs549889950 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132841165 | CTCCTGAAACAATGT[G/T]TTTGATAAACTTGCC | 55743 |
rs550096237 | snp | C/T | | | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132885954 | GATGATATCTAAATA[C/T]TTTCAAAGTTGTAAA | 55743 |
rs550149258 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132878269 | AGGTCAGGAGTTCGA[G/T]ACCAGCCTGGCCAAC | 55743 |
rs550171968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132849884 | CGTGAGCCCATGCCC[A/G]GCCTAGGTGGCCTTT | 55743 |
rs550235353 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CHFR | GRCh38.p7 | 12:132849375 | CCCGGCCTCAGACCC[A/G]TATCGTTTCTTAAAC | 55743 |
rs550437033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132860946 | TTAGTAGAGACGGAG[C/T]TTCACCATGTTGGCC | 55743 |
rs550535563 | in-del | -/A | 0.366266 | 0.221319 | intron-variant | CHFR | GRCh38.p7 | 12:132864176 | AAGTGTTATTATTTG[-/A]AAAAAAAAAAACACA | 55743 |
rs550623249 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132876652 | TTTTAAGTCTTATTT[-/C]TGAGACATACTTAAT | 55743 |
rs550642115 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CHFR | GRCh38.p7 | 12:132889465 | CTGGGCGCAGTGGCT[C/T]ACGTCTGTAATCCCA | 55743 |
rs550679181 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, downstream-variant-500B | CHFR, LOC101928530 | GRCh38.p7 | 12:132889064 | GTAATCCTAGCACTT[C/T]GGGAGGCCGAGGTGG | 55743 |
rs550686189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132854624 | ATCCTGACTAACACG[A/G]TGAAACCCAGTCTCT | 55743 |
rs550718527 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CHFR, LOC101928530 | GRCh38.p7 | 12:132888082 | GCCGGCGTTTTGCGG[A/G]GTCTTCCTGTTCTGA | 55743 |
rs550741643 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132860108 | CCCTCCGTCTCAGCC[C/G]CTCCTCACCCAATTT | 55743 |
rs550749724 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132872954 | AGAGGCCAATGCAGA[C/T]GCTGCTGACCCAGGG | 55743 |
rs550787402 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CHFR | GRCh38.p7 | 12:132863718 | AGCCAGAGTCATAAC[A/G]ACAGGAATGACCTTG | 55743 |
rs550808340 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132887408 | CTCGGCGCCCGCCCC[A/C]CCCCGCGGGCCCCGG | 55743 |
rs550906057 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132853892 | AAGGGCCAGCACGTG[C/T]GCGCACGCCCCGTGC | 55743 |
rs550909225 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132865697 | TGGGCTCTGGCTTTG[C/T]TGCCAAGGCTGGAGT | 55743 |
rs550911213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132871429 | TGCACTCCAGCCTCC[A/G]CAACAGAGCAGAGCG | 55743 |
rs550995416 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132876705 | ATAGACACCAAAGTG[G/T]CACTAAGTGTCCCAT | 55743 |
rs551080759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132843287 | AACTGAGGGTCAGGT[A/G]CAGTGGTTCATGCCT | 55743 |
rs551208143 | snp | A/T | 6.52891e-05 | 0.00571317 | intron-variant | CHFR | GRCh38.p7 | 12:132848272 | TCTAGAAAGAATAAG[A/T]AGTTCAATGATAAAA | 55743 |
rs551269244 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132849296 | TACAGGCGTGATGCA[C/T]TGCACCCGGCCTCAG | 55743 |
rs551357445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132883848 | CTGGGCGAGGTGGCT[C/T]ATGGCTGTAATCCCA | 55743 |
rs551389693 | snp | G/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132882373 | GGAGCCGGGACTCAG[G/T]GGGACCTTTCAGGGT | 55743 |
rs551399785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132877712 | AACTGTGAACACTAC[C/T]GCACTTTGTTTACCA | 55743 |
rs551417145 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132852288 | CCACCGTGCCCGGCC[A/G]ATCTGTTGAAGGTTT | 55743 |
rs551485017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132850014 | GCTGGAGTGCACTGG[C/T]GCCATCTCGGCTCAC | 55743 |
rs551505173 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CHFR | GRCh38.p7 | 12:132889582 | TATATGCCTAGATGG[C/T]CTGAAGTAACTGAAG | 55743 |
rs551520825 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132881932 | GAAGTGGAAAACCTG[C/G]AACTCTCGTACTGTG | 55743 |
rs551653216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132861008 | TCCGTCCACCTTGGC[C/T]TCCCAAAGTGCTGAG | 55743 |
rs551684854 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132849239 | CAGGCATGATGCACT[A/G]CGCCCGGCCTCAGAC | 55743 |
rs551738192 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | CHFR, LOC101928530 | GRCh38.p7 | 12:132888780 | ATCACATGACAAATA[G/T]CAGGCCCTGGAAGAA | 55743 |
rs551745420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132870622 | CTGAGATCGCGCCAC[C/T]GCACTCCAGCCTGGG | 55743 |
rs551750514 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CHFR | GRCh38.p7 | 12:132854407 | CTTCACGTCTAAACA[C/T]TGACGTCACTGCGCA | 55743 |
rs551752478 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132853214 | GAGTGTTCAGGAGGG[A/G]CTACGAATGAACAGT | 55743 |
rs551767356 | snp | G/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132858327 | ATCACACCACTACAC[G/T]CCAGCCTGGGTGACA | 55743 |
rs551790942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132871562 | GGATCACCTGAGGTC[A/G]GGAGTTTGAGACCAG | 55743 |
rs551806768 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132865472 | TGATCCTCCTCTCTC[A/C]GGTGAAACTCCTGTC | 55743 |
rs551812725 | in-del | -/G | 0.00358779 | 0.0422022 | upstream-variant-2KB, nc-transcript-variant | CHFR, LOC101928530 | GRCh38.p7 | 12:132888295 | CTGCACTCATGAGGA[-/G]CCCCCAAGGGCGGTT | 55743 |
rs551933863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132843190 | TGCGGTGGAAACGCA[C/T]GGCCTCTGGTCCCTC | 55743 |
rs551943872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132843842 | TAATCCCAGCTACTC[A/G]GGAGGCTAAGGCAGA | 55743 |
rs552029297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132842743 | CCTTCGACTTAGAAA[C/T]GGCTAAGCCTGAAAT | 55743 |
rs552037051 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, nc-transcript-variant | CHFR, LOC101928530 | GRCh38.p7 | 12:132888190 | CAGAGGGTATTCCCT[C/G]AAAGTGAAAGGTCGG | 55743 |
rs552077610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132853931 | ACCCGCCTACTCTCC[C/T]GTTAAAAGCAGAGCG | 55743 |
rs552124453 | snp | A/C | 0.000333946 | 0.0129175 | intron-variant | CHFR | GRCh38.p7 | 12:132869866 | GCAGAAGCAGCACAC[A/C]ACCAGGGCTCAAGCA | 55743 |
rs552153370 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132847564 | GAGTGTGGGGCTGAG[C/T]GGGCGCCTGCCAGGT | 55743 |
rs552218636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132846844 | GAGATCATGCCACTG[C/T]ACTCCAGTCTGGGCA | 55743 |
rs552265060 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132848498 | ACCTCTGCAGTCCAG[A/C]CAGGAATAGGTATCA | 55743 |
rs552324223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132870261 | GGAGGCTGAGGCAGG[A/G]GAATGGCATGAACCC | 55743 |
rs552387500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132875726 | GAAGGCAGAGTTTGG[A/G]AAAGAGTCACTGCAG | 55743 |
rs552406705 | snp | G/T | | | upstream-variant-2KB | CHFR | GRCh38.p7 | 12:132889379 | GATAATAACAACTCT[G/T]TCAACCAAGTGCCAA | 55743 |
rs552416302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132852230 | CTTGACCTTGTGATC[C/T]GCCCGCCTCGGCCTC | 55743 |
rs552502376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132880837 | AGGCATGGTGGCGGG[C/T]GCCTATAATCCCAGC | 55743 |
rs552519920 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132876251 | TTTATGCAAAATATA[C/T]ATACCAACATATGCA | 55743 |
rs552558543 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132848913 | TGTGATGGCGAGGAG[A/T]TGTATCCCTGAAAAA | 55743 |
rs552565335 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132887041 | ATCATGCGCAAGAAT[A/C]GGTGGGCAGAACACC | 55743 |
rs552569241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132880548 | CTGTAGTCCCAGCTA[C/T]TCAGGAGGCTGAGGC | 55743 |
rs552651960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886661 | TATTAAATAAATAAA[C/T]ATTCTAGGGGCTGGG | 55743 |
rs552703883 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132870690 | TGCTATAGCTCCTAA[C/T]ATGCACCCACTTCTT | 55743 |
rs552744484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132853131 | CAAACCCACTGGGGG[A/G]CATCAGCTGCCCTGA | 55743 |
rs552790168 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132856309 | GGTGCTAATACTATC[C/T]AATATCAGAAAACAA | 55743 |
rs553012411 | snp | C/T | 0.00914312 | 0.0669923 | utr-variant-5-prime, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132887608 | CAAGAGACATTGCGG[C/T]TCCCTCAGCTGATCC | 55743 |
rs553023700 | snp | C/G | | | upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132887799 | TCACGGAAGTGGCTG[C/G]GGTCGGCGCCATGTT | 55743 |
rs553174646 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132842431 | CCCTGTGAGGGAGGC[C/G]CCTTTCTCTGAGTCC | 55743 |
rs553251533 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132864381 | ACTTACAGAATGTAC[C/G]TGGCACACTGCCTCA | 55743 |
rs553314715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132869913 | AAATGCTCTTAAGAA[C/T]GCAACAGCCCCAAGG | 55743 |
rs553369631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132885638 | TGTAATGTCCTACCA[C/T]GTAATAACATGTATA | 55743 |
rs553476481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132841886 | CCGAGGCGGGCGGAT[C/T]ACTTGAGGTCAGGAG | 55743 |
rs553513889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132880616 | TGAGCCAAGATGGTG[C/T]CACTGCACTCCAGCC | 55743 |
rs553536043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132873989 | AGGGGCCCCTACACA[C/T]GTGGTTCCTTCTGCC | 55743 |
rs553572563 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886244 | TGAACCGGGAGGCAG[A/C]GGGTGCAGTGAGCTG | 55743 |
rs553575364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132880173 | CCATCATGCTATAGT[A/G]AACAATACAGTATTG | 55743 |
rs553597628 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CHFR | GRCh38.p7 | 12:132873544 | TCCTGCTCCACAGGG[C/T]TGGCTACGGGGCTGG | 55743 |
rs553674588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132852284 | TGAGCCACCGTGCCC[A/G]GCCGATCTGTTGAAG | 55743 |
rs553722649 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CHFR | GRCh38.p7 | 12:132878591 | GGCTCACACCGAGGC[A/G]GGCAGATCACAAGGT | 55743 |
rs553735979 | snp | C/T | 1.66084e-05 | 0.00288165 | missense | CHFR | GRCh38.p7 | 12:132857508 | CAGGGACGAGCGCTC[C/T]ATCCAGCCCGAGTAG | 55743 |
rs553797443 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132857147 | GGACAGCCCTCACGT[A/G]CCCGGGTGCTGCTGG | 55743 |
rs553903871 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132878260 | TGGATCACGAGGTCA[A/G]GAGTTCGAGACCAGC | 55743 |
rs554064164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132845560 | GAGGCTGAGGTGAGA[C/T]GATCTCTTGAGCCCA | 55743 |
rs554088569 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132884112 | GTGACAGAGTAAGAC[G/T]CCGTCTCAAAAAATA | 55743 |
rs554131476 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132841832 | CAAACATCTGGCCAC[A/G]CACAGTGGCTAATGT | 55743 |
rs554139960 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | CHFR | GRCh38.p7 | 12:132840293 | TCACTCTGCATGGGG[C/T]CTGCCTCCCTCGCAT | 55743 |
rs554326921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132869014 | TGCTGGGGCTGAGGG[A/G]AAGGGGACATGCGGA | 55743 |
rs554369333 | in-del | -/ATTACAGGTGTGAATAAGG | 0.00318978 | 0.0398085 | intron-variant | CHFR | GRCh38.p7 | 12:132864035 | TCCCCAAGTGCTGGA[-/ATTACAGGTGTGAATAAGG]ATTACAGGTGTGAAT | 55743 |
rs554402332 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132884455 | ATAAAATAAATAAAT[A/G]AAATAATCAAGTTCT | 55743 |
rs554447832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132874103 | CTGGAGCCTCCAGAA[A/G]AAACCAGCCCTGTTC | 55743 |
rs554602217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132852382 | GTGTGTTCAATTTCC[A/G]CTCAGGTGAGAGAAC | 55743 |
rs554671088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132863683 | GACTTGTAGGGAGAG[C/T]GCTATCTCCACGAGC | 55743 |
rs554677515 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132840798 | TCACACAAGGGAGCA[A/G]CATGTCCTGGGACCT | 55743 |
rs554687253 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132865753 | TAACCTCTGCCTCCC[A/G]GGCTCAGGCAATCCT | 55743 |
rs554695971 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132879217 | CACCATGCTGGTCTT[C/G]AACTCCTGACCTCTT | 55743 |
rs554740089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132850715 | AGAACCAGTGCTGTG[A/G]TCCTGTGTGCTGCTC | 55743 |
rs554745913 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132841917 | TTCGAGACCAGCCTG[A/G]CCAACATGGTAAAAC | 55743 |
rs554747431 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132884205 | GGGTGGATCACCTGA[A/G]GTCAGGAGTTCAAGA | 55743 |
rs554895850 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132841297 | ATGTTACAGAAAGGC[C/T]TCGTCTCTGCTGCTG | 55743 |
rs554917419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132879484 | CAACCTCTGCCTCCC[A/G]GGTTCAAGCGATTCT | 55743 |
rs554983928 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132861799 | CTCACTCAACTCACA[A/T]CTTAACTCTATTTGT | 55743 |
rs554993068 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CHFR | GRCh38.p7 | 12:132885174 | CAGCACTTTGGGAGG[C/G]TGAGGCAGGCAGATC | 55743 |
rs555092855 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CHFR | GRCh38.p7 | 12:132878479 | AACTGGAAATAAAAA[A/G]AAAAAAAAGCAATTT | 55743 |
rs555240013 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | CHFR | GRCh38.p7 | 12:132877924 | TCTCCTGCCTCAGCC[G/T]CCAGAGTAGCTGGGA | 55743 |
rs555351800 | in-del | -/AATT | 0.0142736 | 0.0832652 | intron-variant | CHFR | GRCh38.p7 | 12:132846341 | ATTTTGGCTCACTGC[-/AATT]AAGCTCCGCCTCCCG | 55743 |
rs555370115 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CHFR | GRCh38.p7 | 12:132848488 | AATTTGACACACCTC[C/T]GCAGTCCAGCCAGGA | 55743 |
rs555424343 | snp | A/G | 0.00159617 | 0.0282053 | downstream-variant-500B | CHFR | GRCh38.p7 | 12:132840100 | CCTTGCACAAACTCA[A/G]GGTCTCTGCATTGTG | 55743 |
rs555446789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132878448 | CACTCCAGCCTTGGC[A/G]ACAGAGCTAGACTCC | 55743 |
rs555447030 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132872845 | GGCTCTGGGCAGAAG[C/T]GGACTAAATGCTGGG | 55743 |
rs555447418 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132866991 | GTGAGCCGAGATTGC[A/G]CCACTGCACTCCAGC | 55743 |
rs555535681 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132860549 | GGGGACCCCTCCTAG[A/C]ACCTTCCTGTCACAG | 55743 |
rs555609623 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132844189 | CCCAACAGCAGCGCA[C/T]GGACTTCACAGCAGT | 55743 |
rs555617824 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132882330 | CTGGAAGCAGCAGAA[C/G]GCAAAGAAACCAGAT | 55743 |
rs555647601 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132876951 | AGGCGCATGCCACAA[C/G]GCCCGGCTAATTTTT | 55743 |
rs555650656 | in-del | -/TAGG | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132849907 | TGGCCTTTTTCTACC[-/TAGG]TATTTTTCCATGTTG | 55743 |
rs555665085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132870486 | CAGTGAGCCGAGATC[A/G]CGCCACTGCACTCCA | 55743 |
rs555795630 | snp | C/T | 0.00199601 | 0.0315281 | intron-variant | CHFR | GRCh38.p7 | 12:132855118 | GTGGTGGCATATGCC[C/T]GTAATCCCAGCCCCT | 55743 |
rs555797881 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132854792 | GCCTGGGCAACAGAG[C/T]GAAACTCCATCTCAA | 55743 |
rs555832893 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132843576 | CCCAGGGCCTAAAAC[A/C]ACCACAGCCCTGTAT | 55743 |
rs555911029 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132865947 | CCAAAGTGCTGGGAT[A/T]ACAGGCGTGAGCCAC | 55743 |
rs556026038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132883563 | ACCCTGTCTCTACTA[A/G]AAATACAAAAAAAAT | 55743 |
rs556112941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132878530 | AGCTAACCTGATGAG[C/T]ATTATTAGAACTTTA | 55743 |
rs556125300 | in-del | -/TTAT | 0.00557542 | 0.0525036 | intron-variant | CHFR | GRCh38.p7 | 12:132849945 | TTGGCTTTGTAGACG[-/TTAT]TTATTTATTTATTTA | 55743 |
rs556147286 | in-del | -/TCT | | | intron-variant | CHFR | GRCh38.p7 | 12:132880269 | AAAGACAGGCAAAAA[-/TCT]TAGTGCCGTTGGGTC | 55743 |
rs556171602 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132862471 | TAACTAGGCGTGACA[A/G]TACGAGCATATGGTC | 55743 |
rs556233254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132861940 | GCAAACCCACATACC[C/T]GTGGTCATATGATAC | 55743 |
rs556233412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132867999 | GATCCAATTTAGAGA[A/G]TCCATATGTACACAT | 55743 |
rs556276289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132845523 | GGCATGGTAGCACAC[A/G]CTTGTGGTCCCAGCT | 55743 |
rs556293907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132867460 | CAAAGGTCCCTTCTC[C/T]GGAGGCTTCCTGGTG | 55743 |
rs556381926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132866404 | ATGTTACAACAGACC[A/G]GAACACCACACCGGA | 55743 |
rs556395444 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | CHFR | GRCh38.p7 | 12:132840183 | TGTGGCTTCCCAGCA[C/T]TGGCAGAATGAAGAG | 55743 |
rs556409226 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132856896 | CACTTGCCTGGGTGC[C/T]GGTGGAGGGACCGCC | 55743 |
rs556411110 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132877966 | CGCCATCACGCCTGG[C/G]TAATTTTTTGTGTTT | 55743 |
rs556524631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132844577 | GCGTGAGCCACTGCG[C/T]CCGGCCACCAATTTA | 55743 |
rs556550560 | snp | A/G | 1.71405e-05 | 0.00292745 | intron-variant | CHFR | GRCh38.p7 | 12:132843992 | AAGCCAACCCAGACA[A/G]AACTAGAGCCATGAG | 55743 |
rs556584103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132871696 | AGAATTGCTTGAACC[C/T]GGCAGGTGGAGATTG | 55743 |
rs556631590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132854871 | GCACTTTGGGAGGCC[A/G]AGGCGGGCTAATCAC | 55743 |
rs556688453 | in-del | -/AA | 0.276267 | 0.248616 | intron-variant | CHFR | GRCh38.p7 | 12:132842109 | GCGAGACTCCATCTC[-/AA]AAAAAAAAAAAAAAA | 55743 |
rs556865760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132851847 | GCACCTGAGACAGCC[A/G]GGGAAGAAGCAGACC | 55743 |
rs556929071 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132859426 | CGCGATCTCGGCTCA[A/C]TGCAAGCTCCGCCTC | 55743 |
rs557000710 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132871175 | TTTCAGGGGTGGCCA[A/G]GTGCAGTGGCTCTTG | 55743 |
rs557203968 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132887836 | GGGCAGAAGGGACGG[A/G]GAACTTCCGGATTGG | 55743 |
rs557215580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886840 | ACCGGTTGCTTTAAG[A/G]GTGTGGTGTTTCATG | 55743 |
rs557287128 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132873847 | TTCCAAACAAAAATC[G/T]GATTATTTCACTCCT | 55743 |
rs557337430 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132869920 | CTTAAGAATGCAACA[C/G]CCCCAAGGCCAGGCA | 55743 |
rs557345127 | snp | G/T | | | upstream-variant-2KB, nc-transcript-variant | CHFR, LOC101928530 | GRCh38.p7 | 12:132888160 | CGTTCACGTGTGTGC[G/T]CCAGAGAAGGGCGCC | 55743 |
rs557346100 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CHFR | GRCh38.p7 | 12:132841951 | ATCTCTACTAAAAAT[A/G]TTTAAAAAATTAGCC | 55743 |
rs557434381 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132864488 | AATTTTTATTTTTTA[C/T]TATTTTTATTTTCTT | 55743 |
rs557461509 | snp | C/T | 1.66051e-05 | 0.00288137 | missense | CHFR | GRCh38.p7 | 12:132844086 | AGCTCACGGAAGCTG[C/T]GCAGGCCACAGCAGT | 55743 |
rs557523087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132843692 | AGAGTGCTGGCCGAG[C/T]GTGGTGGCTCATGCC | 55743 |
rs557562025 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CHFR | GRCh38.p7 | 12:132880692 | CAATTCTGGGCCAGG[C/T]GTGGTGGCTCACACC | 55743 |
rs557662715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132847899 | TGGAATACGGAAAAA[A/G]CAGACAAACACCAAT | 55743 |
rs557708769 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | CHFR | GRCh38.p7 | 12:132889145 | ACCCCGTCTTAGCTG[A/G]ACATGATGACAGCAC | 55743 |
rs557722006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132853021 | ATTAAGCCAACTCTG[A/G]TGACGCAGGGCAGCT | 55743 |
rs557780660 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132871759 | CCTGGGCAACAAGAG[C/T]GAAACTCTATCTCAA | 55743 |
rs557834827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132877841 | GGAGTCTCGCTCTGT[C/T]GCCCAGGCTGGAGTG | 55743 |
rs557936838 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132882178 | AACTAACAAGCCATG[C/G]TGCATCCAAACCACA | 55743 |
rs557987436 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132849009 | TGGAGTACAGGGGAA[C/T]AATCACAGCTCACTG | 55743 |
rs558037750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132854687 | ATCGGGAGCCTGTAG[C/T]CCCAGCTACTCGGGA | 55743 |
rs558042110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132880979 | CAACAACAACAAAAA[A/G]AGTAAGGCTGGGGGC | 55743 |
rs558080896 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132887565 | CGCCCCGCGCCGAAC[A/C]CGGAACCGGCTGCGC | 55743 |
rs558098789 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132860421 | TCATGTTTGCTAGAA[G/T]TAAAATTTCCTCATT | 55743 |
rs558103643 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132880711 | GTGGCTCACACCTGT[A/C]ATCTCAGCACGTTGG | 55743 |
rs558156375 | snp | C/T | 3.30366e-05 | 0.00406413 | missense | CHFR | GRCh38.p7 | 12:132847063 | AGCAGAAACACTCCC[C/T]GCTGGAGAGCCACGA | 55743 |
rs558162279 | snp | C/T | 0 | 0 | intron-variant | CHFR | GRCh38.p7 | 12:132859511 | GCCCACCACCACGCC[C/T]GGCTAATTTTGTGTA | 55743 |
rs558168942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886882 | GTGAATTTTCCACTT[C/T]TCCTTCTATTATTTT | 55743 |
rs558179651 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CHFR | GRCh38.p7 | 12:132875595 | ACCAACAGCACTTCA[A/G]CCTGAGCCACAGAGC | 55743 |
rs558196044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132848361 | GATCAGCTCTCCGAG[C/T]CTCCCCAGCACCTGG | 55743 |
rs558248529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132858228 | AGCCAGATGTGGTGA[C/T]GCATGCCTGTAGTCC | 55743 |
rs558306010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132864343 | CCGTGCTCAGCCAAC[A/G]TGGAGAGGAGCACCA | 55743 |
rs558309903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132857709 | TCAGTCTTGGTTAAT[A/G]AAAAGAAATCAGAGG | 55743 |
rs558316909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132870612 | CTGCAGTGAGCTGAG[A/G]TCGCGCCACCGCACT | 55743 |
rs558346825 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132867775 | TGAGCCCAGACGACA[C/T]GAAGAAAGCCGTGAG | 55743 |
rs558346895 | snp | A/G | 0.000778513 | 0.0197142 | synonymous-codon, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132887232 | ACTCCCGCTTCCTCA[A/G]GAGGACGTGCGGCTC | 55743 |
rs558378924 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132876170 | CACAGTGAAACTCCA[C/T]CTCAAAAAAAAAAAA | 55743 |
rs558456083 | snp | A/G | 2.65671e-05 | 0.00364457 | intron-variant | CHFR | GRCh38.p7 | 12:132843127 | TGAGATGTATTGCAC[A/G]CACCCACTCAGCTAC | 55743 |
rs558516677 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CHFR | GRCh38.p7 | 12:132847949 | GGCTGCACCAGTGAG[A/G]AAACATGGCTCCCGG | 55743 |
rs558653207 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132846411 | GGGACTACAGGCGCC[C/T]GCCACCACGCCCGGC | 55743 |
rs558707066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132874291 | ATGCCCTGAAGCAGG[C/T]GGGACGGCCCAGGAC | 55743 |
rs558874089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132874769 | GGCCCTGGAACAGGC[A/G]GGACTACCCAGGACC | 55743 |
rs559005678 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132856770 | CGTGCCCGGGTGCTG[C/G]TGGAGGGACTGCCCT | 55743 |
rs559081200 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132879603 | ACAATGTTGGCCAGG[A/G]TGGTCTCGATCTCTT | 55743 |
rs559117503 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132847602 | TGGCAAGCCTCAAGG[A/C]CCCACCATTGTGTGT | 55743 |
rs559155204 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | CHFR | GRCh38.p7 | 12:132857135 | GTGCTGGTGGAGGGA[C/T]AGCCCTCACGTGCCC | 55743 |
rs559168585 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132885549 | TTTTGCTGGCAACAT[G/T]ATTTATAAATTCACT | 55743 |
rs559183212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132852534 | TGCGAGGTCAACATG[C/T]CGGCCATAAGGACGG | 55743 |
rs559215834 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132847962 | AGGAAACATGGCTCC[C/T]GGCTCCCCAACCCGC | 55743 |
rs559233136 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CHFR | GRCh38.p7 | 12:132884366 | TGGAGGTTGAGCCAA[A/G]AAGGCACCACTGCAC | 55743 |
rs559246989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132857840 | GAAGGTTGTCACTCT[C/T]GAGTTCCCGCGGAAA | 55743 |
rs559247151 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132851986 | AAGATCTGTTGCAAG[G/T]TCTCTTTTTTTTTTT | 55743 |
rs559250795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886958 | GAACGTGACAATATT[A/G]CATTCTGGAGAGTAT | 55743 |
rs559344166 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | CHFR | GRCh38.p7 | 12:132866493 | TGTTACAACACAGCA[G/T]GTAACACCAAATGTT | 55743 |
rs559434476 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132842166 | TTTTTTTAGAGAAGA[C/G]AATAAAAGCTGCACC | 55743 |
rs559497873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132847299 | ACGGCCTGCAGCACG[A/G]GAAGTCTTGTCCAAG | 55743 |
rs559662191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132868265 | GGGAGGCCGATCGGA[C/T]AGATCACGAGGTCAG | 55743 |
rs559705268 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132841422 | AGAAGAGTCACCCCA[G/T]AGCACCTGTCGGAGA | 55743 |
rs559742338 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CHFR | GRCh38.p7 | 12:132863442 | ACCCAGGAGGCGGAG[C/T]TGCAGCGAACGAAGT | 55743 |
rs559846731 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132881984 | AAGCACATGGGAAAC[A/C]ATGCGGCAGTTTCTC | 55743 |
rs559888766 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132845430 | GCCATTGCACTCCAG[C/G]CTGGGTGACACAGCA | 55743 |
rs559950143 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132850875 | AAAAAAAAGGCAAAG[A/G]ACATAGACAGACATT | 55743 |
rs560029291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132845982 | GTTACCCAATAAATA[C/T]GAAGGGCTGTAGAAG | 55743 |
rs560061557 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132884605 | GTTAAATGAGGTCAC[G/T]AGGTGGGAATCAGAT | 55743 |
rs560066373 | snp | A/G | 0.000821825 | 0.0202543 | synonymous-codon | CHFR | GRCh38.p7 | 12:132857559 | CATGCAGGGCTGCAA[A/G]CTGAAAGTGCAAGAG | 55743 |
rs560082639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132879298 | CCGCACCTGGCCTGC[A/G]ATAGGCATTTGTACA | 55743 |
rs560105630 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132883586 | AAAAAAATTAGCCGG[A/G]CATGGTGGCGGGTGC | 55743 |
rs560209247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132877757 | AACTCAGGATCCCCA[C/T]TGTACATATGTAAAA | 55743 |
rs560248012 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132856892 | CCCTCACTTGCCTGG[G/T]TGCTGGTGGAGGGAC | 55743 |
rs560258739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132872534 | AAATACGTAACGATG[C/T]ACACATCCACGCACC | 55743 |
rs560281132 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132882598 | GCTCTTCCCATTCCA[A/T]TGAGCGTTAACTGCC | 55743 |
rs560323066 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132862280 | AACTCCCTCTGGGGA[A/G]AAAAAAATAAAAATA | 55743 |
rs560347761 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132878769 | AGCTTGCAGTGAGCC[A/G]ATATGGCGCCACTGC | 55743 |
rs560376333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132855733 | CGATTATGACACACG[C/T]ATGAATGGCTGGGTA | 55743 |
rs560376442 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132862067 | CACCTGAGGTCAGGA[A/G]GTCGAGACCAGCCTG | 55743 |
rs560410993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132880432 | GAGGCCAAGGGGGGG[A/G]CGGATCACAAGGTCA | 55743 |
rs560413643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132844451 | CACCACACCGGGCTA[A/G]TTTTTTGTATTTTTA | 55743 |
rs560433355 | snp | C/T | 0.000399281 | 0.0141238 | missense | CHFR | GRCh38.p7 | 12:132861547 | GACGCAGTCTTTCTG[C/T]CTGGGAGAGCTGAGG | 55743 |
rs560437092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132860797 | TGTTCTTGTTGCCCC[A/G]GCTGCAGTGCAATGG | 55743 |
rs560445376 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132855430 | CCAGCACTTTGGGAG[G/T]TCGAGGCCGGCGGAT | 55743 |
rs560516934 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132849731 | CTCCCCAGTAGCTGG[G/T]ATTACAGATGCCCAC | 55743 |
rs560568555 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132872149 | TTCACGGCAGGAACC[C/G]ATGTGAGCAAGAAAT | 55743 |
rs560669545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132850146 | TTTTAGTAGAGATGG[A/G]ATTTCACCATGTTAG | 55743 |
rs560709767 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132840970 | AAATACCATACTATA[C/T]CCAATTTTAGTCAAT | 55743 |
rs560715119 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132842456 | GAGTCCACACAACAT[C/G]TCGTCCTGAGGGCAC | 55743 |
rs560844559 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132858493 | ACTTTAGGAGGCAAA[C/T]GTGGGCAGATCACCT | 55743 |
rs560851725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132868186 | ACTCTGAAAACACCA[C/T]GCTAAGTGAAAGAGC | 55743 |
rs560870647 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132881741 | GGCATGGTGGCACGT[C/G]CCTGTAGTCCCAGCT | 55743 |
rs560915939 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132846159 | ACAGCAGTAACTGCT[A/G]TAGTGAGGGTCTCAA | 55743 |
rs560964381 | snp | A/G | 8.23649e-05 | 0.00641683 | intron-variant | CHFR | GRCh38.p7 | 12:132856636 | CGACTCTTGTCTAGA[A/G]TTGAAAGGACACAGC | 55743 |
rs560981225 | snp | A/G | 8.86454e-05 | 0.00665694 | intron-variant | CHFR | GRCh38.p7 | 12:132851600 | AACCCGCCTGCGTGC[A/G]GTGGCGCGGGCACTC | 55743 |
rs560991371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132844580 | TGAGCCACTGCGCCC[A/G]GCCACCAATTTATTT | 55743 |
rs561038235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132872625 | CACTACACCTCCTCA[C/T]GTGCTTGGCAGCTCT | 55743 |
rs561077202 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132875268 | TGATCTTTACCAAAC[-/A]AAAAAAAATCCTGCA | 55743 |
rs561087370 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132862638 | CTCTGTTGCCCAGGC[A/T]GGAGTGCAGTGGCTC | 55743 |
rs561090729 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132843216 | CCCTCCATAACTAGT[C/T]TCCTCGGACCGTTCT | 55743 |
rs561113348 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132856939 | GGTGCTGGTGGAGGG[A/T]CCACCCTCGCTTGCC | 55743 |
rs561277934 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CHFR | GRCh38.p7 | 12:132878113 | GGCCCATCCTGAACC[C/T]TTCTGAATCCCCACC | 55743 |
rs561332010 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CHFR | GRCh38.p7 | 12:132883160 | TGGCTGGGCGCGGTG[A/G]ATCACACCTGTAATC | 55743 |
rs561407931 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132840362 | GAGCGGAGGAGCAAA[C/T]GCGGCTCATTTATTA | 55743 |
rs561570419 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | CHFR | GRCh38.p7 | 12:132860875 | CTCCTGCCTCAGCCT[A/T]CCAAGTAGCTGGGAT | 55743 |
rs561632913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132866519 | ATGTTACAACACACT[A/G]GAATGTTACAACACA | 55743 |
rs561680616 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132874551 | AAGCCAGGCCCCGGA[A/G]CAGGCGGGACTGCCC | 55743 |
rs561687607 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132876032 | ACACAAAAAAATAGC[C/T]GGGCTTGGTAGTGTG | 55743 |
rs561869854 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CHFR | GRCh38.p7 | 12:132843766 | CCAGCCTGGCCAACA[C/T]GGTGAAACCCCGTCT | 55743 |
rs561944694 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | CHFR, LOC101928530 | GRCh38.p7 | 12:132888517 | ACATTTGTATATATA[C/G]GTATAGGCATAGTTA | 55743 |
rs561956309 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132877091 | TGAGCCACCGCGCCC[A/G]GGCTGATAATAATGT | 55743 |
rs562061055 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CHFR | GRCh38.p7 | 12:132849050 | CTCCTGGGTTCAAGG[A/G]ATCCACCCACCTCAG | 55743 |
rs562126111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132848753 | ACACTCGTTACACGC[A/G]CTCAGCGCTGAGGGC | 55743 |
rs562185483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132853861 | GTGCTCCCAGGAGAC[A/G]ACGCCAGAGCAGGGC | 55743 |
rs562189938 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132865357 | ATTCAAATCTGGCAT[C/G]TTTTCTTTTCTTTTT | 55743 |
rs562208638 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CHFR, LOC101928530 | GRCh38.p7 | 12:132888014 | GGCACAGGGCGCGGT[A/C]CGCGAGTGGGAGCGG | 55743 |
rs562431306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132883339 | GCTGAGGAAGGAGAA[C/T]CACTTGAACCTGGGA | 55743 |
rs562486246 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132857815 | GCAAGTGTTTCTGGC[A/C]CAGAAGTTGGAAGGT | 55743 |
rs562641831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132881831 | TGAGATTGCGCCACT[A/G]CAAATCCAGCCTGGC | 55743 |
rs562690973 | snp | C/T | 2.37747e-05 | 0.00344772 | intron-variant | CHFR | GRCh38.p7 | 12:132877706 | CGTGGTAACTGTGAA[C/T]ACTACTGCACTTTGT | 55743 |
rs562728877 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132872453 | TGGAGTTACAAGATT[C/T]TTTTTCTAGCACCAT | 55743 |
rs562859801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132844249 | GTGAAGACAACGGGC[A/G]ACACATTAGGAAAAT | 55743 |
rs562914058 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132877302 | CCTAGGTATGTAGTA[A/G]GCTACACCATCTAGG | 55743 |
rs562922725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132843806 | CACAAAAAATTAGCC[A/G]GGCGTGGTGGCGGGT | 55743 |
rs562970261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132870683 | AAAGGAATGCTATAG[C/T]TCCTAACATGCACCC | 55743 |
rs562978661 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | CHFR | GRCh38.p7 | 12:132859809 | CACTTTGGGAGGCTG[A/C]GGTGGGCAGATCGCT | 55743 |
rs563031244 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132870256 | ACTCGGGAGGCTGAG[G/T]CAGGAGAATGGCATG | 55743 |
rs563069451 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132843215 | TCCCTCCATAACTAG[G/T]TTCCTCGGACCGTTC | 55743 |
rs563112193 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132855354 | TTGAACCCGGGAGGC[A/G]GAGGTTGCAATGCGC | 55743 |
rs563131888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132842671 | GCTCACGGGACGGAC[A/G]AGAACCCAGCTGTGC | 55743 |
rs563140611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132853904 | GTGCGCGCACGCCCC[A/G]TGCTCCTCAGGACCC | 55743 |
rs563195209 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | CHFR | GRCh38.p7 | 12:132848011 | GATAAACACCAATAG[A/C]ATGCAGAGAACCAGC | 55743 |
rs563202190 | snp | C/T | 6.66945e-05 | 0.00577432 | missense | CHFR | GRCh38.p7 | 12:132859222 | CGTTCAGGTCAAGGT[C/T]CCCATCTACAGGAGA | 55743 |
rs563228075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132876585 | ATTTTTTGATTTGAG[A/G]GAAAGAAATCAAACT | 55743 |
rs563236854 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132880702 | CCAGGCGTGGTGGCT[A/C]ACACCTGTAATCTCA | 55743 |
rs563257184 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132847445 | CACACAGCCCAGCAA[C/T]GAGCCCAGGCTGTTG | 55743 |
rs563291101 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132881055 | GCGGATCACTTCAGA[A/C]CAGGACTTCGAGACC | 55743 |
rs563447706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132875684 | ACAGACTTCCCTTCC[A/G]AGAAATCATCCCAAG | 55743 |
rs563484946 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132868096 | TCTTCCCAATGACCA[C/T]GGAAGAGGTAAGAGT | 55743 |
rs563511087 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132858653 | GAATCGTCTGAACCC[A/G]GGAGGCTGAGGTTGT | 55743 |
rs563545784 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132848376 | TCTCCCCAGCACCTG[C/G]TCTTGGTATCGTAAC | 55743 |
rs563610210 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886568 | CACTTGGGAGACTGG[A/T]GGCAGTGAATGTGGA | 55743 |
rs563625466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132850287 | GTTAGGTAAACCCTC[A/G]CTAAAATTCTCACAG | 55743 |
rs563725767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132859873 | ATAATGAAACCCCAT[C/T]TCTAAAAAAATGGGA | 55743 |
rs563740531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132857878 | AGGCCCTTCCTCAGC[A/G]GCTCCTACGTTCATT | 55743 |
rs563758543 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132874292 | TGCCCTGAAGCAGGC[A/G]GGACGGCCCAGGACC | 55743 |
rs563840755 | snp | C/T | 0.000100346 | 0.00708259 | synonymous-codon, intron-variant | CHFR | GRCh38.p7 | 12:132869641 | GGAGGAACGCTCTCG[C/T]CCTGCAGGAGAAGGC | 55743 |
rs563852229 | snp | C/T | 0.0217685 | 0.102031 | synonymous-codon | CHFR | GRCh38.p7 | 12:132853522 | GCAGTGGGGAGGCTG[C/T]GCCGCCTGCCTTCTG | 55743 |
rs563867715 | snp | G/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132855337 | TGAGGCAGGAGAATC[G/T]CTTGAACCCGGGAGG | 55743 |
rs564048878 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | CHFR | GRCh38.p7 | 12:132875877 | CTCCATAAAACACCG[-/T]TAAGTGAAAAAAGCT | 55743 |
rs564247535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132877085 | CAGGTGTGAGCCACC[A/G]CGCCCGGGCTGATAA | 55743 |
rs564288102 | snp | A/G | 0.00557542 | 0.0525036 | upstream-variant-2KB, nc-transcript-variant | CHFR, LOC101928530 | GRCh38.p7 | 12:132887912 | TAGGAGTAGAAGACG[A/G]TCCATCTTAGTTGTC | 55743 |
rs564308919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132876627 | GCAAGAACCAAAAAT[C/T]ACCAGCATCTTTTAA | 55743 |
rs564369744 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132881111 | ATCTCGACTAAAAAT[A/G]CAAAAAATTAGCCGG | 55743 |
rs564432661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132880872 | CGGGAGGCTAAGGCA[A/G]GAGAATGGTGGGAAC | 55743 |
rs564508500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132887045 | TGCGCAAGAATCGGT[A/G]GGCAGAACACCGAAT | 55743 |
rs564562551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132853357 | GGCAGAGCGCGGCCA[C/T]GTGCACGTCAGCACC | 55743 |
rs564614770 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886436 | TCGCTCCTTTTTAGA[A/G]TATAATGTCGGAGCT | 55743 |
rs564636817 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132879827 | AAAGATACTAGAAGA[A/C]AAAAAAGCGAAGGGT | 55743 |
rs564638646 | in-del | -/A | 0.349671 | 0.229272 | intron-variant | CHFR | GRCh38.p7 | 12:132876173 | GTGAAACTCCATCTC[-/A]AAAAAAAAAAAAGAA | 55743 |
rs564653010 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132857965 | CATCTGTTTGCAGAG[G/T]TCACGGGGTCACACA | 55743 |
rs564654474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132864613 | CATGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 55743 |
rs564702921 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132885776 | ACATAGGCGCAGAAA[G/T]ATGTCGTTAGCCCAG | 55743 |
rs564780111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132857311 | CAGCCCTCACGTGCC[C/T]GGGTGCTGCTGGGTG | 55743 |
rs564784653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132847272 | GTGGCATTTGCAGAG[A/G]GCTGCACGTTCACGG | 55743 |
rs564810555 | snp | C/T | 9.83816e-05 | 0.00701293 | missense, intron-variant | CHFR | GRCh38.p7 | 12:132869670 | GCTCCGTGGAAGAGG[C/T]CGAGGCTGTGGGGAA | 55743 |
rs564865184 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132842026 | GAGGCAAAAGAATTG[C/G]TTGAACCTGGGAGGC | 55743 |
rs564900871 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CHFR | GRCh38.p7 | 12:132862689 | GGTTGACGCCATTCT[C/T]CTGCCTCAGCCTCCC | 55743 |
rs564910193 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132882416 | CTACATCTTGACTGC[A/C]CTGGTGAGTACATTT | 55743 |
rs564953807 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | CHFR | GRCh38.p7 | 12:132845817 | CAGGACCTCTGGATA[C/G]ACAAGTGGTAGAGAC | 55743 |
rs565048496 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132844680 | CTGTCGCCCAGGCTA[C/G]AGTGCAGTGGCGGGG | 55743 |
rs565128269 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132840492 | GAAGCAAAAAAGTTA[C/T]CAGTTTACAAACAAG | 55743 |
rs565193031 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132845354 | ATCCCAGCTACTCAG[A/G]AGGCTGAGGCAGGAC | 55743 |
rs565226297 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132863974 | TTGCCATTTTACCCA[A/G]GCTGGTCTCAAACTC | 55743 |
rs565242720 | in-del | -/C | 0.00518751 | 0.0506641 | intron-variant | CHFR | GRCh38.p7 | 12:132866625 | GAAAGTTACAACACA[-/C]CGCGTAACACCAAAT | 55743 |
rs565310626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132873133 | GACTGAAACCACACA[A/G]GCCTCAGCTCTGCAG | 55743 |
rs565366267 | snp | A/G | 9.3314e-05 | 0.00682996 | missense, intron-variant | CHFR | GRCh38.p7 | 12:132869763 | ACGGAGGGACCCGGG[A/G]ATCGGCCCCTCGCCC | 55743 |
rs565375944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132878687 | AGCCGGGCGTGGTGG[C/T]GGGCGCCTTGTAATC | 55743 |
rs565391074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132873732 | CACAGGGCTGGCTAC[A/G]GGGCTAGAGTGTGCA | 55743 |
rs565505496 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132864273 | ACAGAAGGAAAGAGA[C/G]AGCCTGTGGGCCGGC | 55743 |
rs565513389 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132884244 | ACGAACATGGAGAAA[C/T]CCCGTCTCTACTAAA | 55743 |
rs565555974 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132879861 | GTCAGGAGACAGTGG[A/C]ATGCAAACATACTTT | 55743 |
rs565644778 | snp | C/G | 3.50551e-05 | 0.00418645 | synonymous-codon | CHFR | GRCh38.p7 | 12:132857550 | GAACGTGTGCATGCA[C/G]GGCTGCAAACTGAAA | 55743 |
rs565690439 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CHFR | GRCh38.p7 | 12:132868415 | AATGGCGTGGACCCA[A/G]GAGAATGGCGTGGGA | 55743 |
rs565734748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132841677 | ACAGAGCATCAGAAA[A/G]GCATTCAAATAAACG | 55743 |
rs565759655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132868980 | GGGCCGAGGGGAAGG[A/G]GACATGCGGAGTGAC | 55743 |
rs565784543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132851400 | CCAAGCCGAGCCCCC[A/G]GTGGATGGAGATGTA | 55743 |
rs565784649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132857078 | GAGGGACCACCCTCA[C/T]GTGCCCGGGTGCTGG | 55743 |
rs565796064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132846603 | AACAACCTGAAGGCC[A/G]GGCATAGTGGCTCAC | 55743 |
rs565844477 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132864324 | CGCCATCATCTCCAG[C/T]GCCCCGTGCTCAGCC | 55743 |
rs565883032 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | CHFR | GRCh38.p7 | 12:132863057 | GCCCGCCACCACGCC[A/C]GGCTAATTTTTTGTA | 55743 |
rs565960630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132884142 | AAATATATCAGGCCG[A/G]GCACAGTGGCTCACG | 55743 |
rs565998705 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132885136 | AATTTCTGGCCGGGC[A/G]CGATAGCTCACGCCT | 55743 |
rs566065778 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132840578 | TTCAAGTATTATTCC[A/C]GATGACATGGCAAAG | 55743 |
rs566094636 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132873511 | CCCACACATATGCTG[C/G]ACTGACTTTCTGTGT | 55743 |
rs566122046 | snp | C/T | 0.00557542 | 0.0525036 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132840533 | GATTTCAACAAAAGA[C/T]AAAAAACTTTTTTTT | 55743 |
rs566128545 | snp | C/T | 0.00318978 | 0.0398085 | downstream-variant-500B | CHFR | GRCh38.p7 | 12:132840039 | CGGGACCTCCCCTCC[C/T]GGCCTCACCCCTGCA | 55743 |
rs566176218 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132861771 | ATGACAAGTGGCTTA[A/C]GAGGAGTGTGTGCTC | 55743 |
rs566431208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132875664 | ACATTCTGAGTAACA[C/T]TGACACAGACTTCCC | 55743 |
rs566522917 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132844912 | TGCTGGGATTACAGG[C/T]GTGAGCCTCCACGCC | 55743 |
rs566554610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132877842 | GAGTCTCGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 55743 |
rs566586293 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132850390 | AAATTAGAGTGAAGA[A/G]TTTGGATTCCTGGGG | 55743 |
rs566728902 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132881958 | CTGTGCTGTGGGACT[G/T]CAAAATGGACAAGCA | 55743 |
rs566741579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132876875 | TCTCAGCTCACCACA[A/G]TCTCCGACTCCCGGG | 55743 |
rs566779320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132861033 | GCTGAGATTATAGGC[A/G]GGAGCCACGGTGTCA | 55743 |
rs566785086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132854722 | GAGGCAGGAAAATGG[C/T]GTGAACTCGGGAGGC | 55743 |
rs566786385 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132866270 | AAATCACATCAGAAT[C/G]TTACAACACACCAGA | 55743 |
rs566818059 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132877077 | TGGGATTACAGGTGT[A/G]AGCCACCGCGCCCGG | 55743 |
rs566820097 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132856190 | AAGGGTGTCAGCCGA[A/G]GGTGCAAATGTCTAC | 55743 |
rs566842569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132860434 | AATTAAAATTTCCTC[A/G]TTCCTGTGCTTATTT | 55743 |
rs566845743 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132871600 | AGCATGGCAAAACCC[C/T]GTCTCTACTAAAAAT | 55743 |
rs567012686 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132843432 | CTCTGTCTCAAAAAT[A/C]AATAAATAAATAAAA | 55743 |
rs567050128 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132843903 | GCAGTGAGCCGAGAT[C/T]GCACCACTGCACTCC | 55743 |
rs567073359 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CHFR | GRCh38.p7 | 12:132848857 | TCATGGAAATCGGGG[C/T]GGGGCCACATCCAGC | 55743 |
rs567127826 | in-del | -/AAAT | 0.0142736 | 0.0832652 | intron-variant | CHFR | GRCh38.p7 | 12:132843428 | CAGACTCTGTCTCAA[-/AAAT]AAATAAATAAATAAA | 55743 |
rs567222807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132873816 | CGACTGCAGCCATCA[C/T]TCATCCTCCTGTTCT | 55743 |
rs567264574 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | CHFR | GRCh38.p7 | 12:132840101 | CTTGCACAAACTCAG[G/T]GTCTCTGCATTGTGG | 55743 |
rs567286088 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132873399 | CTGTGTGTGTCTGAG[A/T]TCTGCTGTTACAACA | 55743 |
rs567289002 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132878466 | AGAGCTAGACTCCAA[C/G/T]TGGAAATAAAAAAAA | 55743 |
rs567351744 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132867192 | GCAACGGCATACAAC[C/G]GAGTAAAAACCACAT | 55743 |
rs567371193 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132853309 | CCAATGAGGCCAGGG[C/T]CCAAAGGGGGCGAGC | 55743 |
rs567381796 | snp | A/T | 0.0221141 | 0.102801 | intron-variant | CHFR | GRCh38.p7 | 12:132845467 | CATCTCAAAAAAAAA[A/T]ATAAATAAATAAATA | 55743 |
rs567391191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132884000 | TGGCACACGCCTGAA[A/G]TCTCAGCTAGTCTGG | 55743 |
rs567430632 | snp | A/G | | | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132841444 | TGTCGGAGACCCTGC[A/G]TCCCTTCCCTCAGGG | 55743 |
rs567446897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132844928 | GTGAGCCTCCACGCC[C/T]GGCCCCACATGGATA | 55743 |
rs567446909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132851023 | TGAGACAGGATTTCC[C/T]TCTGTCGCCAAGGCT | 55743 |
rs567475609 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CHFR | GRCh38.p7 | 12:132872201 | TTCCTATGGGAAGGG[A/G]TGTAGCCAGGAGGAA | 55743 |
rs567488046 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132859975 | GTCTGAGCCCAGGAG[A/G]TGGAGGCTGCAGTGA | 55743 |
rs567506407 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132850440 | CATCTGCTGACCACC[A/G]CGTGTGTGAGACATG | 55743 |
rs567515619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132855286 | AATTAGCCAAGTTTG[A/G]TGGTGCATGCCTGTA | 55743 |
rs567584082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132861151 | GGCCTCCCAGTGTTA[A/G]GATTACGGATATGAA | 55743 |
rs567695091 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132849347 | TGAACATTTACAGGC[A/G]TGATGCACTGCACCC | 55743 |
rs567757633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132854546 | TATTTGTTTCTCATG[C/T]CTGTAATCCCAGCAC | 55743 |
rs567841166 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132877444 | GCCGCTGTTATCACA[C/G/T]TAAAGACAGCATTTC | 55743 |
rs567864945 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132877776 | ACATATGTAAAAAAA[A/C]ACACTTGACCAAGAA | 55743 |
rs567876866 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132843949 | AGCGAAACTGTCTCA[A/G]AAAAAAAAAAGAGAG | 55743 |
rs567899386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132882071 | GCTAAGAGAAAAATG[C/T]ATGTCCCTACAAAGA | 55743 |
rs567899829 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | CHFR | GRCh38.p7 | 12:132844468 | TTTTTGTATTTTTAG[G/T]AGAGACTGGGTTTCA | 55743 |
rs567946206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132882638 | TCCTTCAAGCCCCAA[A/G]ACCAGTGCAAGTCAC | 55743 |
rs568086692 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | CHFR, LOC101928530 | GRCh38.p7 | 12:132888997 | CTCTCTGAAGCCTGC[C/T]GCCTGGAGCGGCATC | 55743 |
rs568126351 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CHFR | GRCh38.p7 | 12:132859382 | TCGAGACAGAGTCTC[A/G]CTCTGTCGCCCAGGC | 55743 |
rs568151313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132860099 | AGGCAGTCACCCTCC[A/G]TCTCAGCCGCTCCTC | 55743 |
rs568419665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132870485 | GCAGTGAGCCGAGAT[C/T]GCGCCACTGCACTCC | 55743 |
rs568422735 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | CHFR | GRCh38.p7 | 12:132842864 | AAACGAAGGGATAAA[G/T]GAAGAGCAGGATTTC | 55743 |
rs568440952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132880894 | GGTGGGAACCCAGGA[A/G]GCGGAGGTTACAGTG | 55743 |
rs568495599 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132887373 | ACGCCCATGGAGACT[C/G]CCGACCCCAGAGGCC | 55743 |
rs568564354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132842441 | GAGGCGCCTTTCTCT[A/G]AGTCCACACAACATC | 55743 |
rs568625063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132847827 | CGGGAACAAGAGCTG[C/T]GGGAAGCGGCTCCTA | 55743 |
rs568653694 | in-del | -/TGAGGCAGGAAA | 0.0119091 | 0.0762411 | intron-variant | CHFR | GRCh38.p7 | 12:132868388 | CAGCTACTCAGAGGC[-/TGAGGCAGGAAA]TGAGGCAGGAAAATG | 55743 |
rs568659596 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886803 | CAAAACAAGGTCCCC[A/G]TTGTAAAGACTTATT | 55743 |
rs568719593 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132877833 | CTTGAGACGGAGTCT[C/T]GCTCTGTCGCCCAGG | 55743 |
rs568722392 | snp | A/G | | | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886546 | GGAAATCAAACAACC[A/G]GATGGTCACTTGGGA | 55743 |
rs568772747 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132858066 | TGCCACGAGTAGAAT[C/G]AAAGTGGTAGCCATG | 55743 |
rs568801667 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132879635 | ACCTCGTGATATGCC[C/T]GCCTCGGCTTCTCAA | 55743 |
rs568863641 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CHFR | GRCh38.p7 | 12:132849376 | CCGGCCTCAGACCCG[C/T]ATCGTTTCTTAAACT | 55743 |
rs568913851 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132856024 | ATAACGTCCTGACAA[A/G]TGATAAACATTGCAA | 55743 |
rs568924507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132854644 | ACCCAGTCTCTACCA[A/G]AAATACAAAAAATTA | 55743 |
rs568926466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132854217 | TTTTTTTCATAAGGA[A/G]AAAATGTAAATGAAA | 55743 |
rs568963318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132882150 | CAGTATAAATGTCCA[C/T]CCACTGGTTGTAAAC | 55743 |
rs568963398 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | CHFR | GRCh38.p7 | 12:132889512 | AGGCAGGTGGATCAT[A/G]TCAGGCCTCTGAACC | 55743 |
rs569000044 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CHFR | GRCh38.p7 | 12:132889080 | GGGAGGCCGAGGTGG[C/G]TGGATCGCTTGAGCC | 55743 |
rs569041020 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132874635 | AGGACCAGCACCCAG[A/C]GCGGGGAAGCCAGGC | 55743 |
rs569062926 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132873020 | GTGCCTCCTGGGGAC[C/T]TCTGAGCAGAGACCT | 55743 |
rs569100596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132860142 | TCCTCGGAGGAAAAC[C/T]ATTTTCATGTCTTTG | 55743 |
rs569162141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132866241 | ACCTGAGAAGTCCTC[C/T]CAGGTGAGTCCCGAA | 55743 |
rs569193107 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132871222 | TCTGGGAGGCCGAGG[C/T]GGGCGGATTACCTGA | 55743 |
rs569195851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132887426 | CCGCGGGCCCCGGCC[C/T]GGCCGCCCGCGCCCA | 55743 |
rs569248113 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132865722 | TGGAGTGCAGTGGTG[C/T]AATCTCAGCACATTG | 55743 |
rs569252728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132876749 | AAATACATCTTCTAA[C/T]ACCTTGGGAGCCTAA | 55743 |
rs569389463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132843303 | CAGTGGTTCATGCCT[A/G]TAATCCCAGCACTTT | 55743 |
rs569395973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132875924 | TCACGCCTGTAATCC[C/T]AGCACTTTGGGAGGC | 55743 |
rs569405311 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132884701 | TGAGGACACAGCAAG[-/A]AAAGTGGCCACCTGC | 55743 |
rs569453586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132848782 | GCTGTCTCCAACACA[A/G]TTCGTCAGCACCAGG | 55743 |
rs569457576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132880925 | AGCCGAGATCACGCC[A/G]CTGCACTCCAGCCTG | 55743 |
rs569529060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132869043 | GAGTGACTGCTGCTG[A/G]GGTCGAGGGGAAGGG | 55743 |
rs569754513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132852118 | CCTCCCGAGTAGCTG[A/G]GACTACAGGTGCCTG | 55743 |
rs569756753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132846403 | GAGTAGCTGGGACTA[C/T]AGGCGCCCGCCACCA | 55743 |
rs569764731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132875286 | AAAAAATCCTGCAGT[A/G]AGAACAGCACACTCT | 55743 |
rs569803165 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132842348 | TGAAATCTCTTTTTG[G/T]AACAACATGGTCTCT | 55743 |
rs569878095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132868244 | CGCCTGTAATCCTAG[C/T]ACTTTGGGAGGCCGA | 55743 |
rs569909007 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132874750 | ACCCAGCGCGGGGAA[C/G]CCAGGCCCTGGAACA | 55743 |
rs570114988 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132882363 | GTGGCTGCCAGGAGC[C/T]GGGACTCAGGGGGAC | 55743 |
rs570133740 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132853250 | ATCTGATTTCCCAAC[C/T]CAAAATCAGTCACGA | 55743 |
rs570152755 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132885274 | ACCACTGCCAGGCGT[C/G]GTGGTGGGCGCCTGT | 55743 |
rs570201098 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | CHFR | GRCh38.p7 | 12:132857118 | AGCCCTCACGTGCCC[G/T]GGTGCTGGTGGAGGG | 55743 |
rs570224912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132858933 | CTCCACCCACTTATC[C/T]GGGTGACAGAGTAAC | 55743 |
rs570333217 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132881056 | CGGATCACTTCAGAC[C/G]AGGACTTCGAGACCA | 55743 |
rs570346762 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132864353 | CCAACGTGGAGAGGA[A/G]CACCATCTTACCACT | 55743 |
rs570446374 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132887602 | CGCTGTCAAGAGACA[C/T]TGCGGCTCCCTCAGC | 55743 |
rs570508724 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132842410 | AAGGTTTTTATTCCA[C/T]AAAATCCCTGTGAGG | 55743 |
rs570523789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132864892 | TTACCCAGACTACAC[A/G]CTGTGCTATGCACAT | 55743 |
rs570719939 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132869876 | CACACAACCAGGGCT[C/G]AAGCAGACACTCTAG | 55743 |
rs570755288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132875763 | TTATAGTAAGAAAAA[A/G]TCAAAACAATAAATG | 55743 |
rs570785198 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132875385 | GGGGGCTCACACTTG[C/G]AATCCCAGCACTTGG | 55743 |
rs570814826 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132847583 | CGCCTGCCAGGTGTG[A/T]CTGTGGCAAGCCTCA | 55743 |
rs570849679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886696 | GAGATCTTTTTTAAT[A/G]TAAGCACTACAGCTA | 55743 |
rs570879513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132880595 | CCCAGGAGGTGGAGC[C/T]TGCAGTGAGCCAAGA | 55743 |
rs570946321 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CHFR | GRCh38.p7 | 12:132846908 | AACAAACAAAAACAA[C/T]CTGAAAGCATCAGGA | 55743 |
rs570979262 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132845031 | GAAAACCAAATTGCA[C/T]AGAGGAAAGGATTTG | 55743 |
rs571007991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132852263 | AAAGTGCTGGGATTA[C/T]AGGCATGAGCCACCG | 55743 |
rs571101753 | snp | A/G | 4.95487e-05 | 0.00497714 | missense | CHFR | GRCh38.p7 | 12:132857474 | AGATCCGCTCCACGG[A/G]ACAGCGGCAGGTAGG | 55743 |
rs571130425 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132868735 | AAGTGTCTAGAACAG[A/C]AAAATCCAGAGGCCG | 55743 |
rs571172452 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132863513 | TCCGTCTCAAAAAAA[C/T]AAAGTAAAACAAAAC | 55743 |
rs571206161 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132864816 | TTTTAATTACATAAG[C/T]AATATATAAATACGC | 55743 |
rs571208094 | snp | G/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132883847 | TCTGGGCGAGGTGGC[G/T]CATGGCTGTAATCCC | 55743 |
rs571312422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132873456 | TTGAGCTGTGCAGAT[A/G]CACTTATACACGGGT | 55743 |
rs571318680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132873957 | CACGCTCCGACCACA[C/T]AGCCCTGCTTATGCT | 55743 |
rs571355551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132862260 | AGCCTGGGCAACAAG[A/G]GCGAAACTCCCTCTG | 55743 |
rs571390332 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132877992 | TGTTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 55743 |
rs571452651 | in-del | -/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132879385 | TCTGACACTTTGGGA[-/T]TTTTTTTTTCTTTTT | 55743 |
rs571479896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132867236 | AACAGGCCCAGAGAG[C/T]GTGAGAGGTTTCTGG | 55743 |
rs571500723 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132841730 | AGAGCTACCTGAGAA[A/G]GAGTGTGTGTGCTTC | 55743 |
rs571524664 | snp | A/T | 0.0535932 | 0.154675 | intron-variant | CHFR | GRCh38.p7 | 12:132845478 | AAAAAATAAATAAAT[A/T]AATAAAAATAAAAAA | 55743 |
rs571524838 | in-del | -/G | 0.00119856 | 0.0244508 | intron-variant | CHFR | GRCh38.p7 | 12:132855119 | TGGTGGCATATGCCC[-/G]TAATCCCAGCCCCTC | 55743 |
rs571537852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132851232 | CTGGACACAGAAGAT[C/T]CACCTACCTTGGCCT | 55743 |
rs571545118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132866906 | CGTGGTGGTGGTGCG[C/T]GCCTGTGACCCCAGC | 55743 |
rs571562352 | snp | C/T | 0.00159617 | 0.0282053 | downstream-variant-500B | CHFR | GRCh38.p7 | 12:132839968 | GACCTCCCTGCTCAG[C/T]CTCGCCCCTGCACTA | 55743 |
rs571597771 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132855983 | GGCTGGGATTGTCTT[G/T]GCCTGGTGATGGTGC | 55743 |
rs571600151 | snp | C/T | 0.000263613 | 0.0114777 | intron-variant | CHFR | GRCh38.p7 | 12:132856661 | CACAGCGCCATTCAC[C/T]GGCAGTGAGACATGG | 55743 |
rs571733515 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132849860 | CTCCCAAAGTGCTGG[C/G]ATTACAGGCGTGAGC | 55743 |
rs571755085 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CHFR | GRCh38.p7 | 12:132843228 | AGTTTCCTCGGACCG[C/T]TCTGAGATTTCAGGA | 55743 |
rs571771619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132862200 | AAATTGCTTGAACCC[A/G]GGAGGCGGAGGTTGC | 55743 |
rs571830719 | snp | G/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132877208 | ACTCTTACCATTGTG[G/T]TACAACTGCCTATAG | 55743 |
rs571847789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132872696 | TGGACCCGGAGGCCT[C/T]GTCTACAGTGTGGTG | 55743 |
rs571908866 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132878299 | CACAGTGAAACCCCA[A/T]ATCTACTAAAAATAC | 55743 |
rs571973931 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132871249 | CTGAGGTCCCAAGTT[C/G/T]GAGACCAGCCTGGCC | 55743 |
rs572034367 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132881606 | GGCACGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 55743 |
rs572034599 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132865175 | ACGCCACCTCTATTC[C/T]TCTGGGGCTGTCCCT | 55743 |
rs572036778 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132851845 | GTGCACCTGAGACAG[C/G]CGGGGAAGAAGCAGA | 55743 |
rs572049720 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132873035 | TTCTGAGCAGAGACC[A/T]GACAGCAAATCAGGT | 55743 |
rs572049876 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CHFR | GRCh38.p7 | 12:132879154 | GGACTACAGGCATGC[A/G]CCACCATACCCAGCT | 55743 |
rs572098477 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132857172 | TGCTGGGTGGATGCC[C/T]TCACGTGCCCAGGTG | 55743 |
rs572171722 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132863617 | GTGGAGATGGTGCTG[C/T]GTGTGAACTATTTTA | 55743 |
rs572197658 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CHFR | GRCh38.p7 | 12:132881239 | ACTCCAGCCTGGCAA[C/G]AGAGCGAGACTCCAT | 55743 |
rs572218300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132850565 | CGCCCAGATCACCGG[A/G]TGTGTCCCACGGCCA | 55743 |
rs572226108 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132867588 | AAGGCCCTGGTGACC[G/T]CAGGAGTAGCTGAGC | 55743 |
rs572231313 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132880474 | CCATCCTGGCTAACA[C/T]GGTGAAACCACGTCT | 55743 |
rs572274927 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132840774 | CCCCAGGCTCGGGGC[C/T]GCGGTCACTCACACA | 55743 |
rs572278107 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132856049 | TTGCAATTTATACTA[C/T]AGGACTTTATAGTCG | 55743 |
rs572296769 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132861122 | CGCCTGACCTCAAGT[A/G]ATTCTCCTGCCTTGG | 55743 |
rs572333214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132855439 | TGGGAGGTCGAGGCC[A/G]GCGGATCACGAGGTC | 55743 |
rs572416648 | snp | A/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132878381 | GGCTGAGGCAGGAGA[A/T]TCGCATGAACCCAGG | 55743 |
rs572448885 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132844637 | ATATAACATTTATTT[A/T]ATTTATTTTTTGAGA | 55743 |
rs572494989 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132883092 | GCTTGGTGGGTTAAA[C/T]CTTTCAAGCAGTTGA | 55743 |
rs572690372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132861408 | GGAGCATGGCAGCGG[C/T]CCCCGCATGCCCCAG | 55743 |
rs572753556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132866958 | GGAATCACTTGAACC[C/T]GGGAGGCGGAGGTTG | 55743 |
rs572757038 | in-del | -/T | 0.244776 | 0.249945 | intron-variant | CHFR | GRCh38.p7 | 12:132844452 | ACCACACCGGGCTAA[-/T]TTTTTGTATTTTTAG | 55743 |
rs572765702 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132866475 | TGTTACAACACACCA[C/G]AATGTTACAACACAG | 55743 |
rs573002270 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132843745 | GCCGAGGTCAAGAGT[G/T]CGAGACCAGCCTGGC | 55743 |
rs573017098 | snp | C/T | 3.33868e-05 | 0.00408562 | missense | CHFR | GRCh38.p7 | 12:132877615 | ATTCTACAGTGATCT[C/T]CAGAGACCAGTTTAT | 55743 |
rs573050522 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CHFR | GRCh38.p7 | 12:132889148 | CCGTCTTAGCTGGAC[A/G]TGATGACAGCACATG | 55743 |
rs573065760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132849018 | GGGGAACAATCACAG[C/T]TCACTGCAACCTCCG | 55743 |
rs573078497 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132877087 | GGTGTGAGCCACCGC[A/G]CCCGGGCTGATAATA | 55743 |
rs573159272 | snp | A/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132854796 | GGGCAACAGAGCGAA[A/T]CTCCATCTCAAAAAA | 55743 |
rs573243437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132875607 | TCAGCCTGAGCCACA[A/G]AGCGAGACTCCGTCT | 55743 |
rs573246819 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132873441 | CTGGAAGATGCGGTT[C/T]TGAGCTGTGCAGATG | 55743 |
rs573248769 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CHFR | GRCh38.p7 | 12:132852489 | ACAGCCAAGTTCCCT[A/G]GACACTCGCCACCCA | 55743 |
rs573283149 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132865880 | GGTTTCACCATGTTG[C/G]CCAAACTGGTCTTGA | 55743 |
rs573377759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132870615 | CAGTGAGCTGAGATC[A/G]CGCCACCGCACTCCA | 55743 |
rs573392224 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | CHFR, LOC101928530 | GRCh38.p7 | 12:132888560 | AAACCAAAAATAAAA[C/T]TGTAAGCCTCCCCAA | 55743 |
rs573532558 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132861821 | TCTATTTGTGCCTAT[C/G]TCTACGTGGGGTGGA | 55743 |
rs573550529 | in-del | -/A | | | intron-variant | CHFR | GRCh38.p7 | 12:132855244 | GAGACTTTGTCTCGA[-/A]AAAAAAAAAAAAAGA | 55743 |
rs573600991 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132843160 | GAATCCCAGCAGAGA[A/C]CCAACGACAGACGCT | 55743 |
rs573756745 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CHFR | GRCh38.p7 | 12:132866998 | GAGATTGCGCCACTG[C/T]ACTCCAGCCTGGGCA | 55743 |
rs573841653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132882968 | TGGCCTCCCAAACTG[C/T]TGGGATTACAGGCAT | 55743 |
rs573985639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132850059 | CCCGGGTTCACGCCA[C/T]TCTCCTGCCTCAGCC | 55743 |
rs574038401 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132875064 | CAGCACCCAGCATGG[G/T]GAAGCCAGGCCCTGA | 55743 |
rs574066776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132860589 | GGCTGGCTGCTCTCT[A/G]GACTGCTATACAGCA | 55743 |
rs574096035 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132876275 | ATATGCATTTTTAAC[G/T]TATGAATAGGATTTT | 55743 |
rs574165139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132865988 | GCTGAGATGCTTTCA[C/T]CTTGAAGTGTTATTT | 55743 |
rs574206362 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132880857 | ATAATCCCAGCTACA[C/T]GGGAGGCTAAGGCAG | 55743 |
rs574253332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132865394 | GAGACCTGGTCTGTC[A/G]CCCAGGCTGGAGTGC | 55743 |
rs574255301 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132853602 | CAGGGCCGAGCTGTG[G/T]GCAGGCCCCAAGCCT | 55743 |
rs574257230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132847981 | TCCCCAACCCGCAGC[A/G]GGTCAGGTAAAACAG | 55743 |
rs574262218 | in-del | -/A | | | intron-variant | CHFR | GRCh38.p7 | 12:132842186 | AAGCTGCACCTCCTC[-/A]AGGCATCCCCGTGGC | 55743 |
rs574268102 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132878377 | GGGAGGCTGAGGCAG[A/G]AGAATCGCATGAACC | 55743 |
rs574318146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132853165 | AGTGGCTGGGGAGAG[A/G]CCAAGTATTAAGGTC | 55743 |
rs574351058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132843588 | AACAACCACAGCCCT[A/G]TATGGCCTGACGTCC | 55743 |
rs574380779 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132842459 | TCCACACAACATCTC[A/G]TCCTGAGGGCACTGT | 55743 |
rs574388717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132843191 | GCGGTGGAAACGCAC[A/G]GCCTCTGGTCCCTCC | 55743 |
rs574477582 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132842631 | CCACGTGAGGGTGAC[G/T]ATGTGACAGCAATCA | 55743 |
rs574496395 | snp | A/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132887689 | CTCACCAAGAGCGGC[A/T]GCTAAAGCGGAGCCG | 55743 |
rs574501707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132880756 | CGGATCACAAGGTCA[A/G]GAGTTCAAGACCAGC | 55743 |
rs574563095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886961 | CGTGACAATATTGCA[C/T]TCTGGAGAGTATATG | 55743 |
rs574698387 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132864391 | TGTACCTGGCACACT[C/G]CCTCACATTTAGTAG | 55743 |
rs574731102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132857848 | TCACTCTTGAGTTCC[C/T]GCGGAAAAGCAAGGA | 55743 |
rs574789986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132864099 | GAATAACCTATATCT[C/T]AATAAAGACTTAGTT | 55743 |
rs574904028 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132869934 | AGCCCCAAGGCCAGG[A/C]ACGGTGGTGCAGGCC | 55743 |
rs574910668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132841904 | TTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 55743 |
rs574965534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132875484 | CCATCTGAGCTAGGC[A/G]TGGCGGCGGGCACCT | 55743 |
rs575041669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132879671 | TGGGATTACAGGCGT[A/G]AGCCACCAGCGCCCG | 55743 |
rs575079133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132848933 | TCCCTGAAAAAAGGC[A/G]AGGCTCACATTTTCT | 55743 |
rs575089142 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132874436 | AGCGCGGGGAAGCCA[G/T]GTCCTGATGTAGGCG | 55743 |
rs575126193 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132885673 | GTTACAATAACAATG[A/G]CTAATGCTAAGTGCT | 55743 |
rs575136765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132871729 | GTGAGCTGAGATTGC[A/G]CCATTACACTTCAGC | 55743 |
rs575154606 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132871343 | TGTAATCCCAGCTAC[A/C]TGGAAGGCTGAGGCA | 55743 |
rs575213003 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132852332 | ATAAAGAGAGGACAA[C/G]CCCATAGAACCTATG | 55743 |
rs575218134 | snp | A/C | 1.78541e-05 | 0.00298776 | intron-variant | CHFR | GRCh38.p7 | 12:132877536 | AAGAAACACCAAAAG[A/C]AGCTCAGAACATACT | 55743 |
rs575228523 | snp | G/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132841743 | AAAGAGTGTGTGTGC[G/T]TCTCACAATATCAAA | 55743 |
rs575234288 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132877046 | GTGATCCAACTGCCT[A/C]AGCCTCCCAAAGTGC | 55743 |
rs575439567 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132881709 | CGTCTCTACTAAAGA[C/T]ACAAAAAAATTAGCC | 55743 |
rs575442441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132854017 | GTCTTTTCCACACTT[C/T]CCTTGTACTTCCAAA | 55743 |
rs575456726 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132853727 | ATTCCTGTCCAGCAC[C/G]CCAGTGTTAGAGAGG | 55743 |
rs575487349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132871194 | CAGTGGCTCTTGCCT[A/G]TAATCCCAGCACTCT | 55743 |
rs575518921 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132881064 | TTCAGACCAGGACTT[C/T]GAGACCAGCCTGGCC | 55743 |
rs575519453 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132869937 | CCCAAGGCCAGGCAC[C/G]GTGGTGCAGGCCTGT | 55743 |
rs575526494 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | CHFR, LOC101928530 | GRCh38.p7 | 12:132888363 | GCCTGTAATCTAAGT[C/G]CTTTGGAAGGCCTAG | 55743 |
rs575560080 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886852 | AAGAGTGTGGTGTTT[C/G]ATGTCCACATATCTG | 55743 |
rs575628014 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132858687 | GAGCCAAGACTGTGC[C/G]ACTGCACTCCAGCCT | 55743 |
rs575648025 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886360 | GCAAGCACATTATAA[A/G]GGGTGAAATTAACCA | 55743 |
rs575665546 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132881264 | TCCATCTCAAAAAAA[-/G]AAAAAAAGTAAAAAT | 55743 |
rs575744673 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132865156 | CCACGCTGGAGCGGC[C/T]GGAACGCCACCTCTA | 55743 |
rs575772137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132875548 | GAATCGCTTGAACCC[A/G]GGTGGCGGAGGTTGC | 55743 |
rs575805602 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132870593 | TGAACCCAGGAGGCG[C/G]AGGCTGCAGTGAGCT | 55743 |
rs575805728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132864489 | ATTTTTATTTTTTAT[C/T]ATTTTTATTTTCTTT | 55743 |
rs575815945 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | CHFR, LOC101928530 | GRCh38.p7 | 12:132888166 | CGTGTGTGCTCCAGA[A/G]AAGGGCGCCAGAGGG | 55743 |
rs575834500 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132880693 | AATTCTGGGCCAGGC[G/T]TGGTGGCTCACACCT | 55743 |
rs575862366 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CHFR | GRCh38.p7 | 12:132883155 | GCTCTTGGCTGGGCG[C/T]GGTGGATCACACCTG | 55743 |
rs575866981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132863233 | AAAAAAAATGCCAGG[C/T]GCGGTGGCTCATGCC | 55743 |
rs575952982 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CHFR | GRCh38.p7 | 12:132842487 | TGTCTCCATCACTTT[A/C]ATCTGAACTCCTTGG | 55743 |
rs576014166 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CHFR | GRCh38.p7 | 12:132847942 | ACCAGCTGGCTGCAC[C/T]AGTGAGGAAACATGG | 55743 |
rs576049145 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132865800 | AAGTAGCTGGGATTA[C/G]AGGCATGCACCACCA | 55743 |
rs576074865 | snp | A/C | 1.65463e-05 | 0.00287626 | missense | CHFR | GRCh38.p7 | 12:132847114 | TTCCATGTCAAACCT[A/C]TGGTTGCCAGGTAAT | 55743 |
rs576112639 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132844215 | GCAGTGGGAGACTAA[C/T]GCACTGACCATAAAT | 55743 |
rs576157654 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132857286 | ACGTGCCCGGGTGCT[C/G]GTGGAGGGACAGCCC | 55743 |
rs576197652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132851455 | GATGGTGGGAAAAGA[C/T]AGATTATTCAATATG | 55743 |
rs576197670 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132845229 | GGGAGGCCGAGGCAG[A/G]CGGATCACAAGGTCA | 55743 |
rs576258086 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132850719 | CCAGTGCTGTGGTCC[A/T]GTGTGCTGCTCACAC | 55743 |
rs576267049 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132846663 | AGGTGGGCAGATCAC[C/G]TGAAGTCAGAAGTTC | 55743 |
rs576320121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132874209 | GTTTTTTAAATCCAT[C/T]AAGCTTGTGGTAAAT | 55743 |
rs576324050 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | CHFR, LOC101928530 | GRCh38.p7 | 12:132887962 | GACCCTTTCGGGTAC[A/G]GTTGCACACAGTGGA | 55743 |
rs576384308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132879494 | CTCCCGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 55743 |
rs576391103 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132884805 | TGAAAATAAATTTCT[C/G]GCCAGGCACAGTGGC | 55743 |
rs576408069 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CHFR | GRCh38.p7 | 12:132873634 | TCCTGCTCCACAGGG[C/T]TGGCTACGGGGCTGG | 55743 |
rs576425597 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132840832 | TCCAGCCCCAGGCTC[A/G]GGGCCGCGGTCACTC | 55743 |
rs576589946 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132856761 | CCGCCCTCACGTGCC[C/G]GGGTGCTGGTGGAGG | 55743 |
rs576636067 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132884312 | TAATCCCAGCTACTC[G/T]GGAGGCTGAGGCAGG | 55743 |
rs576655379 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132879797 | TACTGCCTATAATAA[C/T]CTATAAGGATACATA | 55743 |
rs576667508 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132861452 | GACTGAGGACACACA[C/T]AACCAGACACTAACC | 55743 |
rs576721982 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132863891 | TGCCTCCTGAGTATC[C/T]GGGACTACAGGTGTG | 55743 |
rs576725100 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132883796 | AATGCCTTATAAATG[G/T]CAGGCACATCATTGC | 55743 |
rs576736782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132866254 | TCCCAGGTGAGTCCC[A/G]AAATCACATCAGAAT | 55743 |
rs576738395 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132885158 | CTCACGCCTGTAATC[C/T]CAGCACTTTGGGAGG | 55743 |
rs576783769 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132863396 | CCTGTAACCCAGCTA[C/T]TTGGGAGGCTGAGGC | 55743 |
rs576811337 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CHFR | GRCh38.p7 | 12:132847953 | GCACCAGTGAGGAAA[C/T]ATGGCTCCCGGCTCC | 55743 |
rs576821114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886885 | AATTTTCCACTTTTC[C/T]TTCTATTATTTTTAA | 55743 |
rs576848687 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132847399 | CTACACAGCCCAGGT[A/G]TGAATGAGACATGAA | 55743 |
rs576877338 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHFR | GRCh38.p7 | 12:132853049 | GCTTCTGGTGACATC[A/G]CCACTGCTGGGGAGA | 55743 |
rs576891601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132842520 | CACAGGAGTGATTTA[C/T]GTGATCACCTAACCT | 55743 |
rs576943420 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132852510 | TCGCCACCCACACAG[C/G]AAAGACCCTGCGAGG | 55743 |
rs576945941 | snp | A/C | 0.00318978 | 0.0398085 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132841361 | GAGGGCGGGCTGCGG[A/C]CCCCGGGGCTCTGGG | 55743 |
rs577007021 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132840840 | CAGGCTCGGGGCCGC[A/G]GTCACTCACCGGTTA | 55743 |
rs577119809 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132869282 | ACTGCTGGTGGGCAC[C/T]GGTTTCCTTTTCGTG | 55743 |
rs577188916 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132868529 | CAAAAAACAAAAAAA[A/T]ATTAGCTGGGCGTGG | 55743 |
rs577250398 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132874322 | CAGCACCCAGCGTGG[C/G]GAAGCCAGGCCCTGG | 55743 |
rs577261608 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132860007 | CCAAGACTGCACCAC[A/G]GCGCTCTGGCCTAGG | 55743 |
rs577293374 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132854152 | CAGGGGCCAATAAGG[C/G]CAACAGGTAAGACCC | 55743 |
rs577330208 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132875956 | GAGGCAGGCAGATCA[C/T]CTGAGATCAGGAGTT | 55743 |
rs577509473 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132844444 | TGCCCGCCACCACAC[C/T]GGGCTAATTTTTTGT | 55743 |
rs577530692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132885577 | ACTAAAATCGTTCCT[A/G]TTAAAAGATAAACTC | 55743 |
rs577595590 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132863501 | TAAGATCAAAATTCC[A/G]TCTCAAAAAAACAAA | 55743 |
rs577604136 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132856186 | AGGGAAGGGTGTCAG[A/C]CGAGGGTGCAAATGT | 55743 |
rs577659045 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CHFR | GRCh38.p7 | 12:132868003 | CAATTTAGAGAATCC[A/G]TATGTACACATCCTC | 55743 |
rs577681001 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132856771 | GTGCCCGGGTGCTGG[C/T]GGAGGGACTGCCCTC | 55743 |
rs577683095 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132881424 | TAGAAAGTAAATAAT[A/C/G]CAACTTAAAACAATT | 55743 |
rs577788841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132861344 | TGTTACAGGCATCAA[C/T]CTGAGGCAGGGTCCA | 55743 |
rs577789503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132872952 | GGAGAGGCCAATGCA[A/G]ATGCTGCTGACCCAG | 55743 |
rs577820910 | in-del | -/AATAAT | | | intron-variant | CHFR | GRCh38.p7 | 12:132880334 | CACAAACCAGGAAAA[-/AATAAT]AATAATAAGCTGAGG | 55743 |
rs577843987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132872483 | TTAGCAAGCAGCTCG[A/G]TATGACCACTCTGGA | 55743 |
rs577852758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132860677 | AGTGCAGACTTCTCC[C/T]TAAATCATCTTCAAT | 55743 |
rs577967891 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | CHFR | GRCh38.p7 | 12:132840219 | AGCAGGTTTCACAGG[A/C]GTCACTGAGGGACAG | 55743 |
rs578006282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132850103 | GAACTACAGGCGCCC[A/G]CCACCATACACGGCT | 55743 |
rs578039265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132849682 | CTCACTGCAACCTCC[A/G]CCTCCTGGGTTCAAG | 55743 |
rs578055121 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | CHFR | GRCh38.p7 | 12:132855368 | CGGAGGTTGCAATGC[A/G/T]CCAAGATTGTGCCAT | 55743 |
rs578088365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHFR | GRCh38.p7 | 12:132854955 | ACTAAAAATACAAAA[C/T]TAGCGGCCGGGCGCG | 55743 |
rs745321936 | snp | A/G | | | stop-gained, intron-variant | CHFR | GRCh38.p7 | 12:132869640 | TGGAGGAACGCTCTC[A/G]CCCTGCAGGAGAAGG | 55743 |
rs745374934 | snp | G/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132881310 | ATTGTTTAAAAAGAT[G/T]AAAAGACAAGCTATG | 55743 |
rs745429725 | snp | A/G | 1.74592e-05 | 0.00295454 | intron-variant | CHFR | GRCh38.p7 | 12:132851610 | CGTGCGGTGGCGCGG[A/G]CACTCACACTGCTGA | 55743 |
rs745444684 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132853958 | AGCGCGGTGGGCAAC[A/G]TACTGGGAGCCACAC | 55743 |
rs745444738 | snp | C/T | | | downstream-variant-500B | CHFR | GRCh38.p7 | 12:132840263 | GACCATCACTAGCAG[C/T]GAGGCACTCGGAGCT | 55743 |
rs745476803 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132872530 | GTGTAAATACGTAAC[A/G]ATGCACACATCCACG | 55743 |
rs745511558 | in-del | -/A | | | intron-variant | CHFR | GRCh38.p7 | 12:132845468 | TCTCAAAAAAAAAAA[-/A]TAAATAAATAAATAA | 55743 |
rs745529097 | snp | C/G | 1.6566e-05 | 0.00287797 | synonymous-codon | CHFR | GRCh38.p7 | 12:132857496 | GCAGGTAGGACACAG[C/G]GACGAGCGCTCCATC | 55743 |
rs745530337 | snp | A/C | 1.64901e-05 | 0.00287137 | intron-variant | CHFR | GRCh38.p7 | 12:132870703 | AACATGCACCCACTT[A/C]TTTGCTACACTCTTA | 55743 |
rs745544421 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132842374 | TCTCTTCCATGTGCT[A/G]TTTGTGCTCAAACAC | 55743 |
rs745575260 | in-del | -/A | | | intron-variant | CHFR | GRCh38.p7 | 12:132843559 | AGTAACTGCAAATAG[-/A]ACCCAGGGCCTAAAA | 55743 |
rs745584051 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132882094 | TACAAAGACTGCACA[C/T]TTATGTTTATATTAG | 55743 |
rs745612571 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132848078 | CCAGCCCGCAGCGAG[C/T]CGGTACCTTCAGGAT | 55743 |
rs745615761 | snp | A/C | 1.64727e-05 | 0.00286986 | synonymous-codon | CHFR | GRCh38.p7 | 12:132856542 | TTCTTCATCAGAAAA[A/C]GACCGCCTGACTTTG | 55743 |
rs745735958 | snp | C/T | 1.96292e-05 | 0.00313276 | missense | CHFR | GRCh38.p7 | 12:132843038 | GCTTTCACCTGAGTG[C/T]GGCAGTTACGGCCCC | 55743 |
rs745763828 | snp | C/G | 6.60371e-05 | 0.0057458 | missense | CHFR | GRCh38.p7 | 12:132861470 | CCAGACACTAACCTC[C/G]TCTCATTTTCTTCTT | 55743 |
rs745782659 | snp | A/G | 0.000445534 | 0.0149187 | utr-variant-5-prime, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132887330 | TCGGGCCGCTCCATC[A/G]GGATTCACATCTGCG | 55743 |
rs745800820 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132849245 | TGATGCACTGCGCCC[A/G]GCCTCAGACCCACAT | 55743 |
rs745811402 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132876881 | CTCACCACAATCTCC[A/G]ACTCCCGGGTTCAAG | 55743 |
rs745853838 | snp | C/T | 6.23228e-05 | 0.00558189 | intron-variant | CHFR | GRCh38.p7 | 12:132877691 | AACACGGGATATGAT[C/T]GTGGTAACTGTGAAC | 55743 |
rs745889598 | snp | A/G | 1.64846e-05 | 0.0028709 | missense | CHFR | GRCh38.p7 | 12:132859173 | TCGTGGACGGTTTGG[A/G]CATTTCTACGCGGTT | 55743 |
rs745974025 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132865865 | TTTTTGTAAAGATAC[A/G]GTTTCACCATGTTGC | 55743 |
rs746076985 | in-del | -/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132867968 | AAAATTAAAAAAAAA[-/T]TAATATGTATAGCGC | 55743 |
rs746118089 | snp | A/G | 0.00013132 | 0.00810201 | intron-variant | CHFR | GRCh38.p7 | 12:132848630 | ACTGGGGCCTGAAGA[A/G]CCAGTATTACCACAA | 55743 |
rs746172062 | snp | C/G/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132844617 | AGCAAAACAATCCCA[C/G/T]GTGGATATAACATTT | 55743 |
rs746181525 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132872862 | GACTAAATGCTGGGC[C/T]GTCAGCTGCAGGACA | 55743 |
rs746187833 | snp | A/G | 9.44599e-05 | 0.00687176 | missense, intron-variant | CHFR | GRCh38.p7 | 12:132869760 | ACGACGGAGGGACCC[A/G]GGGATCGGCCCCTCG | 55743 |
rs746343089 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132861994 | AACAGAGCTTTGGGC[C/T]GGGTGCGGTGGCTCA | 55743 |
rs746360566 | snp | A/C | 0.000118085 | 0.00768299 | missense | CHFR | GRCh38.p7 | 12:132853553 | TACTCAGGACACTGC[A/C]GGCACACGACGTATG | 55743 |
rs746371244 | snp | A/C | 3.08152e-05 | 0.00392513 | intron-variant | CHFR | GRCh38.p7 | 12:132844159 | ACACAGCCAGTTACC[A/C]AGCAACACCATCTTC | 55743 |
rs746380972 | snp | C/T | 1.67175e-05 | 0.0028911 | synonymous-codon | CHFR | GRCh38.p7 | 12:132853450 | CGTCAGGCTGACGGA[C/T]GTGGAGGGTGCATCC | 55743 |
rs746414469 | snp | C/T | 3.29647e-05 | 0.00405971 | synonymous-codon | CHFR | GRCh38.p7 | 12:132859142 | GTCTGGCTTCCCAGC[C/T]GCTGCTCTGACGTCC | 55743 |
rs746460075 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132852908 | AGCAGGGCAGAGAAG[C/T]GAAGCCTCCATACCC | 55743 |
rs746470663 | snp | A/G | 1.65455e-05 | 0.00287619 | missense | CHFR | GRCh38.p7 | 12:132857411 | CTCACTTGCCTGGAT[A/G]CTGGATGAGGTATGC | 55743 |
rs746554223 | snp | C/T | 5.14955e-05 | 0.00507396 | missense | CHFR | GRCh38.p7 | 12:132851630 | CACACTGCTGAGGGG[C/T]GACACGCGGGTCCTG | 55743 |
rs746590937 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132878438 | CGCGCCACTGCACTC[A/C]AGCCTTGGCGACAGA | 55743 |
rs746652873 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132881080 | GAGACCAGCCTGGCC[A/G]ACAGGATGAGACCCC | 55743 |
rs746739997 | in-del | -/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132870531 | AGCAAAACTCCGTCT[-/C]AAAAAAAAAAAAAAA | 55743 |
rs746741984 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132858373 | TCCAAAAAACAAAAA[C/T]AAAAACAAAAAACCA | 55743 |
rs746754478 | in-del | -/A | 1.65265e-05 | 0.00287454 | intron-variant | CHFR | GRCh38.p7 | 12:132872399 | TTCCACTGGTGCTGT[-/A]AAAAAACAAAAACAC | 55743 |
rs746777781 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132870330 | GCACTCCAGCCTGGG[C/T]GACAAAGCGCGACTC | 55743 |
rs746789487 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132869355 | TCCACTGAAATGTAC[A/G]CTTCGGCTGGATGAC | 55743 |
rs746850522 | snp | C/T | | | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132841279 | TCTCGGCGGGACGGC[C/T]GCATGTTACAGAAAG | 55743 |
rs746869999 | snp | A/G | 6.59152e-05 | 0.00574049 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132841539 | TGCTGAAAGCTGCTC[A/G]GGGCCTCTGGATGCT | 55743 |
rs746923680 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132847206 | AACGAGAGAAAACAT[C/T]TCATAAAAGGCCCCT | 55743 |
rs746925087 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132865910 | AACTCCTGGGCTCAA[C/G]GGATCTGCCCACCTT | 55743 |
rs746930809 | snp | A/G | 8.8032e-05 | 0.00663387 | intron-variant | CHFR | GRCh38.p7 | 12:132851606 | CCTGCGTGCGGTGGC[A/G]CGGGCACTCACACTG | 55743 |
rs746949286 | snp | C/T | 0.000158053 | 0.00888827 | intron-variant | CHFR | GRCh38.p7 | 12:132848754 | CACTCGTTACACGCA[C/T]TCAGCGCTGAGGGCT | 55743 |
rs747008143 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132876849 | TCCCAGGCTGGAGTG[A/C]AGTGGTGCCATCTCA | 55743 |
rs747067060 | snp | A/G | | | upstream-variant-2KB | CHFR | GRCh38.p7 | 12:132889231 | GGAGGACAAGGCTGC[A/G]GTAAACCACAGTCTG | 55743 |
rs747113652 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132875666 | ATTCTGAGTAACACT[A/G]ACACAGACTTCCCTT | 55743 |
rs747129595 | snp | G/T | 6.05199e-05 | 0.00550057 | intron-variant | CHFR | GRCh38.p7 | 12:132848268 | AGATTCTAGAAAGAA[G/T]AAGAAGTTCAATGAT | 55743 |
rs747154221 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132847963 | GGAAACATGGCTCCC[A/G]GCTCCCCAACCCGCA | 55743 |
rs747198621 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132865818 | GCATGCACCACCACA[C/G]CCGGCTAATTTTTGT | 55743 |
rs747214956 | snp | A/G | 1.6531e-05 | 0.00287493 | intron-variant | CHFR | GRCh38.p7 | 12:132872239 | AGAGCGCCCTCACGT[A/G]CACCCCCGTGCGGGT | 55743 |
rs747235725 | snp | A/T | 3.29468e-05 | 0.00405861 | intron-variant | CHFR | GRCh38.p7 | 12:132856635 | GCGACTCTTGTCTAG[A/T]ATTGAAAGGACACAG | 55743 |
rs747306800 | snp | A/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132856009 | GGTGCCTCTTCTGTA[A/T]TAACGTCCTGACAAA | 55743 |
rs747349751 | in-del | -/CT | | | intron-variant | CHFR | GRCh38.p7 | 12:132866828 | TATGCTTTTAGAACA[-/CT]CTGCTCCTGGTGACC | 55743 |
rs747380214 | snp | C/G | 1.66952e-05 | 0.00288917 | missense | CHFR | GRCh38.p7 | 12:132853442 | TCACCTGTCGTCAGG[C/G]TGACGGACGTGGAGG | 55743 |
rs747517165 | snp | A/G | 3.29598e-05 | 0.00405941 | synonymous-codon | CHFR | GRCh38.p7 | 12:132859166 | GACGTCCTCGTGGAC[A/G]GTTTGGGCATTTCTA | 55743 |
rs747548627 | snp | A/C | 1.68917e-05 | 0.00290613 | intron-variant | CHFR | GRCh38.p7 | 12:132851776 | GGAGCACGTGGGACC[A/C]AGGGCAGAAAGACAG | 55743 |
rs747559390 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132883076 | ATTTGCTGCGCTTGA[C/T]GCTTGGTGGGTTAAA | 55743 |
rs747568800 | snp | A/G | 3.46099e-05 | 0.00415978 | intron-variant | CHFR | GRCh38.p7 | 12:132859064 | AGGGTGAACACGGTC[A/G]CACCTCACGCAGTCG | 55743 |
rs747621911 | snp | A/G | 0.000285551 | 0.0119455 | intron-variant, synonymous-codon | CHFR | GRCh38.p7 | 12:132862412 | AGCCTGGGCAACACA[A/G]CAAGGCACCATCTCT | 55743 |
rs747650904 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132861875 | CAGAGAAACAAATGC[A/G]GAGATGTCTGTGACC | 55743 |
rs747697880 | snp | A/G | 1.68168e-05 | 0.00289967 | synonymous-codon | CHFR | GRCh38.p7 | 12:132844108 | CACAGCAGTAACACA[A/G]AACGGTGTCTCCCGT | 55743 |
rs747787830 | snp | A/C/T | 3.36068e-05 | 0.00409908 | intron-variant | CHFR | GRCh38.p7 | 12:132844013 | GAGCCATGAGGAAGT[A/C/T]GGGGGCTCCTTACCT | 55743 |
rs747879114 | snp | A/G | 1.66349e-05 | 0.00288395 | intron-variant | CHFR | GRCh38.p7 | 12:132856734 | TGCTGCGGAAGGAGG[A/G]GTCTGGGCGGACCGC | 55743 |
rs747932956 | snp | C/T | 1.85561e-05 | 0.00304594 | intron-variant | CHFR | GRCh38.p7 | 12:132877517 | AGGCTTCTTAAGCTA[C/T]AAGAAGAAACACCAA | 55743 |
rs747960278 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132852743 | GTCCGTTCCGTCCAC[A/G]GGTTCTACAAGAAGC | 55743 |
rs748026869 | snp | C/T | 1.71211e-05 | 0.00292579 | intron-variant | CHFR | GRCh38.p7 | 12:132848750 | AGGACACTCGTTACA[C/T]GCACTCAGCGCTGAG | 55743 |
rs748084235 | snp | G/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132868389 | CAGCTACTCAGAGGC[G/T]GAGGCAGGAAAATGG | 55743 |
rs748096866 | snp | C/T | 1.66427e-05 | 0.00288462 | intron-variant | CHFR | GRCh38.p7 | 12:132857395 | TGCTGGTGTGGATGC[C/T]CTCACTTGCCTGGAT | 55743 |
rs748099881 | in-del | -/T | 2.13081e-05 | 0.00326399 | intron-variant | CHFR | GRCh38.p7 | 12:132877695 | GGGATATGATCGTGG[-/T]TAACTGTGAACACTA | 55743 |
rs748110156 | snp | C/G | 9.39364e-05 | 0.00685269 | missense, intron-variant | CHFR | GRCh38.p7 | 12:132869733 | CCTCAAAGCACACCT[C/G]AGTGGCGGGCGACGA | 55743 |
rs748112188 | snp | A/G | 4.97591e-05 | 0.00498769 | intron-variant | CHFR | GRCh38.p7 | 12:132856725 | CGTGCGCAGTGCTGC[A/G]GAAGGAGGGGTCTGG | 55743 |
rs748158399 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132846957 | GGGTGGGTGAAGGTC[A/G]GAGTTGTCACTGGGA | 55743 |
rs748195198 | in-del | -/AT | 2.92154e-05 | 0.00382189 | intron-variant | CHFR | GRCh38.p7 | 12:132848236 | ACACTGAGGATAAAC[-/AT]ATTTCTTTTCATTAC | 55743 |
rs748253107 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132865356 | TATTCAAATCTGGCA[C/T]GTTTTCTTTTCTTTT | 55743 |
rs748257912 | in-del | -/CA | | | intron-variant | CHFR | GRCh38.p7 | 12:132870531 | AGCAAAACTCCGTCT[-/CA]AAAAAAAAAAAAAAA | 55743 |
rs748276125 | in-del | -/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132844474 | TATTTTTAGTAGAGA[-/C]TGGGTTTCACCGTGT | 55743 |
rs748283036 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132858071 | CGAGTAGAATGAAAG[C/T]GGTAGCCATGCGGGG | 55743 |
rs748309050 | snp | G/T | 3.29457e-05 | 0.00405854 | missense | CHFR | GRCh38.p7 | 12:132856594 | ATTTTATTTCTGGCA[G/T]CCATACTTTGCACAT | 55743 |
rs748314312 | snp | C/T | 1.64735e-05 | 0.00286993 | synonymous-codon | CHFR | GRCh38.p7 | 12:132856503 | GTCAACGTCTGACAG[C/T]TCCAGCAGGTCCTCT | 55743 |
rs748380162 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132875571 | GAGGTTGCAGTGAGC[C/T]GAGATCGCACCAACA | 55743 |
rs748387119 | snp | A/T | 1.66774e-05 | 0.00288763 | intron-variant | CHFR | GRCh38.p7 | 12:132861447 | GAGAGGACTGAGGAC[A/T]CACACAACCAGACAC | 55743 |
rs748419509 | snp | G/T | 2.40382e-05 | 0.00346677 | synonymous-codon | CHFR | GRCh38.p7 | 12:132853567 | CCGGCACACGACGTA[G/T]GGCTGGCTGCAAGGA | 55743 |
rs748507238 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132854145 | CCAAGGCCAGGGGCC[A/G]ATAAGGCCAACAGGT | 55743 |
rs748561227 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132876445 | ATGCTCAACTGGTAA[C/G]TATAATGAAAATATT | 55743 |
rs748573732 | snp | C/G | 1.64846e-05 | 0.0028709 | intron-variant | CHFR | GRCh38.p7 | 12:132872276 | CCGGCAAGCCTTCCT[C/G]TCTCTTACTGTGTTC | 55743 |
rs748583625 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132854970 | TTAGCGGCCGGGCGC[A/G]GTGGCTCACACCTAT | 55743 |
rs748587949 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132882308 | TGTGACCCTGTGTCA[C/T]GACACGCTGGAAGCA | 55743 |
rs748671960 | in-del | -/CCT | | | intron-variant | CHFR | GRCh38.p7 | 12:132845951 | GCTGCCCAGTTGTTA[-/CCT]CCTCCTTGCTCTTGT | 55743 |
rs748721756 | snp | C/T | 1.64947e-05 | 0.00287177 | synonymous-codon | CHFR | GRCh38.p7 | 12:132848145 | CAGACACTTGTCACC[C/T]AGGTTGAGCTCTGCC | 55743 |
rs748750259 | snp | C/G | 0.000216153 | 0.0103937 | intron-variant | CHFR | GRCh38.p7 | 12:132870835 | CCCTGTGCAAACTGA[C/G]AACTCATTTTTCTCT | 55743 |
rs748758310 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132859639 | ACAGGTGTGAGCTAC[C/T]GCGCCCCACCCTCTT | 55743 |
rs748764333 | snp | A/G | 1.93714e-05 | 0.00311213 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132887345 | GGGATTCACATCTGC[A/G]GAGACCCCGGAAACG | 55743 |
rs748832380 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132883029 | TTCTAATCTGGAACC[A/G]AGATGCTTTGTGCTA | 55743 |
rs748952886 | snp | A/G | 1.66651e-05 | 0.00288657 | synonymous-codon | CHFR | GRCh38.p7 | 12:132851688 | GGGCTGGAAGCAGCA[A/G]GTGCACAGGGCGTGG | 55743 |
rs749026084 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132851346 | TAACAGTGACACATT[A/G]TAAAGCAACCACAGT | 55743 |
rs749026459 | snp | A/G | | | downstream-variant-500B | CHFR | GRCh38.p7 | 12:132840128 | GTGGCTTCTTCTGGT[A/G]CTCAGCTGAAGACAA | 55743 |
rs749127983 | snp | C/T | 1.67047e-05 | 0.00288999 | intron-variant | CHFR | GRCh38.p7 | 12:132848176 | GAGATGAAGGGGCAA[C/T]GTTACCTGTTTATAA | 55743 |
rs749186808 | snp | C/T | | | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132841479 | GTGAAAACACCTTGA[C/T]GTGCTTGTCTCTGTA | 55743 |
rs749192848 | snp | A/C | 1.64855e-05 | 0.00287097 | missense | CHFR | GRCh38.p7 | 12:132861582 | GCTGGAGACTTCATC[A/C]CTTGCCACAGAGGGA | 55743 |
rs749209980 | in-del | -/A | | | intron-variant | CHFR | GRCh38.p7 | 12:132863210 | CTGACCTCATTTCTT[-/A]AAAAAAAAAAAAAAA | 55743 |
rs749219400 | snp | C/T | 1.6937e-05 | 0.00291002 | intron-variant | CHFR | GRCh38.p7 | 12:132844004 | ACAGAACTAGAGCCA[C/T]GAGGAAGTCGGGGGC | 55743 |
rs749219860 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132866957 | GGGAATCACTTGAAC[C/T]CGGGAGGCGGAGGTT | 55743 |
rs749221911 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132880231 | ACAAATGTAAAATCT[A/G]AAACTATGAAACTTC | 55743 |
rs749243668 | snp | A/G | 0.000282686 | 0.0118854 | intron-variant, missense | CHFR | GRCh38.p7 | 12:132862387 | CACTTGATCCCAGGA[A/G]TTTTAGACCAGCCTG | 55743 |
rs749373830 | snp | A/G | 0.00023753 | 0.0108953 | synonymous-codon | CHFR | GRCh38.p7 | 12:132853561 | ACACTGCCGGCACAC[A/G]ACGTATGGCTGGCTG | 55743 |
rs749382720 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132849078 | CAGCCTCCTGAGTAG[C/G]TAGGACTACAGGTGC | 55743 |
rs749387187 | snp | A/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132867701 | TCTTCTGTTCATAGG[A/T]ATCTGCAGACTGCTA | 55743 |
rs749391173 | in-del | -/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132877834 | TGAGACGGAGTCTCG[-/C]CTCTGTCGCCCAGGC | 55743 |
rs749403779 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132856213 | ATGTCTACAGCAGTC[A/G]CCTGCGGCTGACGCT | 55743 |
rs749465714 | snp | C/G | 1.67683e-05 | 0.00289549 | intron-variant | CHFR | GRCh38.p7 | 12:132859236 | TCCCCATCTACAGGA[C/G]AAAGGGATGTGTTCT | 55743 |
rs749471534 | in-del | -/AAC | 1.64738e-05 | 0.00286995 | cds-indel | CHFR | GRCh38.p7 | 12:132872358 | GCATGTCTGCTTCTT[-/AAC]AACCTTCAGCTTGTT | 55743 |
rs749507220 | snp | A/G | | | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886829 | TTATTTGACCCACCG[A/G]TTGCTTTAAGAGTGT | 55743 |
rs749514804 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132865501 | TCTCAGCTTCCTGAG[C/T]AGCTGGGACTACAGG | 55743 |
rs749534217 | in-del | -/CAC | | | intron-variant | CHFR | GRCh38.p7 | 12:132864188 | TTTGAAAAAAAAAAA[-/CAC]AAGAAACTGGCTTAC | 55743 |
rs749537035 | snp | A/C/G | 3.29915e-05 | 0.00406138 | missense | CHFR | GRCh38.p7 | 12:132859183 | TTTGGGCATTTCTAC[A/C/G]CGGTTGTGCGACCAA | 55743 |
rs749543398 | in-del | -/G | 1.64792e-05 | 0.00287042 | intron-variant | CHFR | GRCh38.p7 | 12:132856666 | CGCCATTCACCGGCA[-/G]TGAGACATGGCAGGC | 55743 |
rs749601873 | snp | A/G | 1.65952e-05 | 0.00288051 | missense | CHFR | GRCh38.p7 | 12:132857504 | GACACAGGGACGAGC[A/G]CTCCATCCAGCCCGA | 55743 |
rs749603865 | snp | A/G | 3.31098e-05 | 0.00406864 | intron-variant | CHFR | GRCh38.p7 | 12:132870824 | AAAGTGGTGGCCCCT[A/G]TGCAAACTGAGAACT | 55743 |
rs749617163 | snp | A/C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132863306 | TGAGGTCAGGAGTTC[A/C/G]AGACCAGCCTGACCA | 55743 |
rs749668647 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132873774 | GCATGCAGGGGGCTG[C/G]AGCCAATCCCCCCAG | 55743 |
rs749767207 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132853047 | CAGCTTCTGGTGACA[C/T]CGCCACTGCTGGGGA | 55743 |
rs749809573 | snp | G/T | 1.64855e-05 | 0.00287097 | intron-variant | CHFR | GRCh38.p7 | 12:132856461 | CTGAGCCAGGGGCAT[G/T]ATTTACCTAATGTCT | 55743 |
rs749821203 | snp | A/G | 0.000115633 | 0.00760283 | synonymous-codon | CHFR | GRCh38.p7 | 12:132847086 | AGCCACGAGGCTCTC[A/G]GTCAACATGTTTTTC | 55743 |
rs749838905 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132866500 | ACACAGCATGTAACA[C/T]CAAATGTTACAACAC | 55743 |
rs749973618 | snp | A/G | 1.64904e-05 | 0.00287139 | synonymous-codon | CHFR | GRCh38.p7 | 12:132848103 | CAGGATGTCTGACTC[A/G]TAGCTGTTGTTGTTC | 55743 |
rs750011459 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132864909 | TGTGCTATGCACATT[A/G]GTGGATAGGAACAGG | 55743 |
rs750039103 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132882828 | CTCCCACTTCAGCCT[C/T]CTGAGTAGCTGAGAC | 55743 |
rs750067972 | snp | C/G/T | 3.30864e-05 | 0.00406723 | intron-variant | CHFR | GRCh38.p7 | 12:132870821 | AGAAAAGTGGTGGCC[C/G/T]CTGTGCAAACTGAGA | 55743 |
rs750100419 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132855751 | GAATGGCTGGGTAGA[A/G]GCAGCAAAATCTTAA | 55743 |
rs750109543 | snp | C/T | 1.65029e-05 | 0.00287248 | intron-variant | CHFR | GRCh38.p7 | 12:132848036 | ACCAGCTGGCTGCAC[C/T]AGGGAGAAAATGTGG | 55743 |
rs750119581 | snp | G/T | 3.29451e-05 | 0.00405851 | synonymous-codon | CHFR | GRCh38.p7 | 12:132856578 | CAGCATGTCTTGAGT[G/T]ATTTTATTTCTGGCA | 55743 |
rs750158136 | in-del | -/A | 1.72615e-05 | 0.00293776 | intron-variant | CHFR | GRCh38.p7 | 12:132843982 | AGAAGCCAAGAAGCC[-/A]ACCCAGACAGAACTA | 55743 |
rs750205050 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132872144 | CACTATTCACGGCAG[A/G]AACCCATGTGAGCAA | 55743 |
rs750256598 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132871353 | GCTACCTGGAAGGCT[C/G]AGGCAGGAGAATCGC | 55743 |
rs750260902 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132858167 | TTCGAGACCAGCCTG[A/G]CTAATATGGTGAAAC | 55743 |
rs750304472 | snp | A/T | | | splice-acceptor-variant | CHFR | GRCh38.p7 | 12:132856632 | ACTGCGACTCTTGTC[A/T]AGAATTGAAAGGACA | 55743 |
rs750312312 | snp | A/G | 3.35289e-05 | 0.0040943 | intron-variant | CHFR | GRCh38.p7 | 12:132851749 | ACTGCTGAAGCACAC[A/G]CACATTCAGCCGGAG | 55743 |
rs750405934 | snp | C/T | 3.78029e-05 | 0.00434742 | intron-variant | CHFR | GRCh38.p7 | 12:132859032 | GAAGAACCTGCAGTG[C/T]CATGTTCCGTGAGCC | 55743 |
rs750466757 | snp | A/G | 1.66407e-05 | 0.00288446 | missense | CHFR | GRCh38.p7 | 12:132877600 | TTTTCATCCACTACA[A/G]TTCTACAGTGATCTC | 55743 |
rs750545709 | snp | A/G | 3.58957e-05 | 0.00423634 | intron-variant | CHFR | GRCh38.p7 | 12:132851590 | GACAGATAGGAACCC[A/G]CCTGCGTGCGGTGGC | 55743 |
rs750582504 | snp | A/G | 6.27254e-05 | 0.00559989 | intron-variant | CHFR | GRCh38.p7 | 12:132848736 | GCACCTGTGGAGAGA[A/G]GACACTCGTTACACG | 55743 |
rs750629677 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132867656 | CTTTCCTGTCAGATC[A/G]AAACACAGCCTAATC | 55743 |
rs750639185 | snp | A/G | 3.36576e-05 | 0.00410215 | intron-variant | CHFR | GRCh38.p7 | 12:132857377 | CGCCCTCACGTGCCC[A/G]GGTGCTGGTGTGGAT | 55743 |
rs750811776 | snp | G/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132868104 | ATGACCATGGAAGAG[G/T]TAAGAGTCATGCCGT | 55743 |
rs750855275 | snp | A/G | 1.65015e-05 | 0.00287237 | intron-variant | CHFR | GRCh38.p7 | 12:132856448 | CACACACTCTGCTCT[A/G]AGCCAGGGGCATGAT | 55743 |
rs750874709 | in-del | -/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132882539 | TGCAAACATTCTGTA[-/C]TATTGGAAGTACTGT | 55743 |
rs750893196 | snp | G/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132883343 | AGGAAGGAGAATCAC[G/T]TGAACCTGGGAGGCG | 55743 |
rs750897572 | snp | G/T | 3.74272e-05 | 0.00432576 | intron-variant | CHFR | GRCh38.p7 | 12:132877669 | CCTAAAAAAGAGAGG[G/T]TGGGTCAACACGGGA | 55743 |
rs750955936 | snp | C/T | 1.64781e-05 | 0.00287033 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132841517 | AACACGCTCTCTTCA[C/T]CTCCAGTGCTGAAAG | 55743 |
rs750993967 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132875973 | TGAGATCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 55743 |
rs751083450 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132879669 | GCTGGGATTACAGGC[A/G]TGAGCCACCAGCGCC | 55743 |
rs751187101 | in-del | -/ACAG | | | upstream-variant-2KB, downstream-variant-500B | CHFR, LOC101928530 | GRCh38.p7 | 12:132888719 | AGCGTCGACGTTAAA[-/ACAG]ACAGACAACTTAAGG | 55743 |
rs751193384 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132864824 | ACATAAGTAATATAT[A/G]AATACGCTGCCCTTT | 55743 |
rs751231369 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132847343 | TCCCAAAAGGTTCCA[A/G]TGTAACAGTTACCAG | 55743 |
rs751314685 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132842207 | TCCCCGTGGCATCTG[C/T]TGACAGGGCTGAGGC | 55743 |
rs751415679 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132882069 | TAGCTAAGAGAAAAA[C/T]GTATGTCCCTACAAA | 55743 |
rs751426380 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132854713 | CGGGAGGCTGAGGCA[A/G]GAAAATGGCGTGAAC | 55743 |
rs751429614 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132871284 | CGGCGAAACCCTGTC[C/T]GTACTAAAAATACAA | 55743 |
rs751440176 | snp | A/C | 8.37177e-05 | 0.0064693 | missense | CHFR | GRCh38.p7 | 12:132851659 | TGCTCGCGCTCCGCT[A/C]TCCGGTCGGGCATGG | 55743 |
rs751498855 | snp | A/G | 1.70886e-05 | 0.00292301 | missense | CHFR | GRCh38.p7 | 12:132857539 | CAAGCCGCGCAGAAC[A/G]TGTGCATGCAGGGCT | 55743 |
rs751516879 | snp | A/G | 1.65367e-05 | 0.00287543 | intron-variant | CHFR | GRCh38.p7 | 12:132870818 | ATCAGAAAAGTGGTG[A/G]CCCCTGTGCAAACTG | 55743 |
rs751524285 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132860315 | GATTACATTAGTTCA[C/T]GATACTGTATTTGTA | 55743 |
rs751592981 | snp | A/G | | | missense | CHFR | GRCh38.p7 | 12:132861515 | CCTCCTGATCCTGGG[A/G]TTCCAACGACGAAAA | 55743 |
rs751655100 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132860519 | CACGTGTCAGATAAC[A/C]TAATTTCTTTCCCTG | 55743 |
rs751674449 | snp | A/G | 1.68875e-05 | 0.00290576 | intron-variant | CHFR | GRCh38.p7 | 12:132857373 | GGACCGCCCTCACGT[A/G]CCCGGGTGCTGGTGT | 55743 |
rs751789347 | snp | A/G | 9.87216e-05 | 0.00702503 | synonymous-codon, intron-variant | CHFR | GRCh38.p7 | 12:132869665 | AGAAGGCTCCGTGGA[A/G]GAGGCCGAGGCTGTG | 55743 |
rs751878497 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132867251 | CGTGAGAGGTTTCTG[A/G]TTTCAAGAAGGCACA | 55743 |
rs751887961 | in-del | -/CATATATA | | | intron-variant | CHFR | GRCh38.p7 | 12:132850964 | AACTGTATGTGTGTG[-/CATATATA]TATATATATATATAT | 55743 |
rs751902652 | in-del | -/A | 0.00737247 | 0.0602651 | intron-variant | CHFR | GRCh38.p7 | 12:132862445 | AAAAATACAAAAAAG[-/A]AAAAAAAAATTAACT | 55743 |
rs751925400 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132879686 | GAGCCACCAGCGCCC[A/G]GCCCTGAATACAAAA | 55743 |
rs751995061 | snp | C/G | 1.80481e-05 | 0.00300395 | intron-variant | CHFR | GRCh38.p7 | 12:132851577 | CTGACCCCTGAAGGA[C/G]AGATAGGAACCCGCC | 55743 |
rs752016583 | snp | C/T | 1.65784e-05 | 0.00287905 | missense | CHFR | GRCh38.p7 | 12:132859209 | ACCAACAACTGCCCG[C/T]TCAGGTCAAGGTCCC | 55743 |
rs752027164 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132866770 | TACAACACATCTGGA[C/T]GTTACTCTTCAGATG | 55743 |
rs752032125 | snp | A/C | 1.64784e-05 | 0.00287035 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132841508 | TATTTTAAAAACACG[A/C]TCTCTTCACCTCCAG | 55743 |
rs752048632 | in-del | -/A | 3.12358e-05 | 0.00395183 | intron-variant | CHFR | GRCh38.p7 | 12:132844162 | AGCCAGTTACCCAGC[-/A]AACACCATCTTCCCA | 55743 |
rs752063969 | snp | C/G | | | upstream-variant-2KB | CHFR | GRCh38.p7 | 12:132889087 | CGAGGTGGGTGGATC[C/G]CTTGAGCCCAGGAAT | 55743 |
rs752104453 | snp | A/G | 0.000299506 | 0.0122337 | missense | CHFR | GRCh38.p7 | 12:132877594 | CCTGATTTTTCATCC[A/G]CTACAATTCTACAGT | 55743 |
rs752129222 | snp | C/T | 1.69269e-05 | 0.00290915 | intron-variant | CHFR | GRCh38.p7 | 12:132872421 | CAAAAACACAATTTA[C/T]TCTACTTAAAATAAC | 55743 |
rs752131350 | snp | A/G | 6.61124e-05 | 0.00574907 | intron-variant | CHFR | GRCh38.p7 | 12:132856711 | CTGCTGGGAGCTCGC[A/G]TGCGCAGTGCTGCGG | 55743 |
rs752233501 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132884698 | CATGTGAGGACACAG[A/C]AAGAAAGTGGCCACC | 55743 |
rs752245469 | in-del | -/A | | | intron-variant | CHFR | GRCh38.p7 | 12:132854948 | GTCTCTACTAAAAAT[-/A]ACAAAATTAGCGGCC | 55743 |
rs752281100 | snp | C/T | 1.65179e-05 | 0.00287379 | missense | CHFR | GRCh38.p7 | 12:132859195 | TACGCGGTTGTGCGA[C/T]CAACAACTGCCCGTT | 55743 |
rs752333209 | snp | A/C/G | 0.000232732 | 0.0107853 | missense | CHFR | GRCh38.p7 | 12:132853436 | CGCGGCTCACCTGTC[A/C/G]TCAGGCTGACGGACG | 55743 |
rs752336193 | snp | A/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132879952 | TCACTGACCTATGGG[A/T]GTGTGAATCAGAAGA | 55743 |
rs752473859 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132853638 | GTAGGGCCGGTGCAA[C/G]GCGGGTCCGCAGCCA | 55743 |
rs752483839 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132881037 | TTTGGGTGGCCAAGG[C/T]GGGCGGATCACTTCA | 55743 |
rs752504914 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132872177 | AATGGGGTGTAGCCA[A/G]GAGGAACGTTCCTAT | 55743 |
rs752548854 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132881904 | GACTGACCACCTACA[A/G]GTGGCCAAAAGGGAA | 55743 |
rs752563941 | snp | G/T | 3.32989e-05 | 0.00408024 | intron-variant | CHFR | GRCh38.p7 | 12:132847147 | TGTGACGCAAAAAAA[G/T]AGAGGAATAAGAAAT | 55743 |
rs752604065 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132854511 | GCTGTACATGCAGCC[A/G]AATCCCAGCTTCATA | 55743 |
rs752604410 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132863894 | CTCCTGAGTATCTGG[A/G]ACTACAGGTGTGCAC | 55743 |
rs752636689 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132862537 | TGAGCCCGGGAGTTC[A/G]AGGCTACAGTGAGCC | 55743 |
rs752654129 | snp | C/T | 1.65364e-05 | 0.0028754 | intron-variant | CHFR | GRCh38.p7 | 12:132847015 | CACTCACATGCGCCT[C/T]AGAGCAGGAGGCAAC | 55743 |
rs752825922 | snp | C/G | 1.72639e-05 | 0.00293796 | intron-variant | CHFR | GRCh38.p7 | 12:132861641 | CCCCAGACCCTGTGA[C/G]AGGAATCAAACAAGA | 55743 |
rs752894210 | snp | C/T | 2.27803e-05 | 0.00337486 | missense | CHFR | GRCh38.p7 | 12:132843012 | CCAGCTGCACTCACA[C/T]GGCGTGGTGAGCTTT | 55743 |
rs752932212 | snp | A/G | 0.000282207 | 0.0118753 | missense, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132887300 | GGCTGCGGCGGCGGC[A/G]ACTGCTTGCCTTCCT | 55743 |
rs752934181 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132860335 | CTGTATTTGTATTAT[C/T]ATGCTTATGCAAGTA | 55743 |
rs752938242 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132847765 | GTCTTGCTAAAGGGC[A/G]GCACCTTCAAGAAGC | 55743 |
rs752938756 | in-del | -/A | | | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886377 | GGTGAAATTAACCAA[-/A]AAAAAAAAAAAAATT | 55743 |
rs752973043 | in-del | -/AA | | | intron-variant | CHFR | GRCh38.p7 | 12:132865307 | AAGGGTACACAGCCC[-/AA]GAGAGCTGGTAAAAC | 55743 |
rs753060082 | snp | A/C | 1.65512e-05 | 0.00287669 | intron-variant | CHFR | GRCh38.p7 | 12:132872399 | TTCCACTGGTGCTGT[A/C]AAAAAACAAAAACAC | 55743 |
rs753088383 | snp | A/C | 3.45214e-05 | 0.00415446 | intron-variant | CHFR | GRCh38.p7 | 12:132848242 | AGGATAAACATATTT[A/C]TTTTCATTACAGATT | 55743 |
rs753097471 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132848852 | GGGTCTCATGGAAAT[C/T]GGGGCGGGGCCACAT | 55743 |
rs753130507 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132876579 | AAAATGATTTTTTGA[C/T]TTGAGGGAAAGAAAT | 55743 |
rs753178130 | snp | C/T | 6.6072e-05 | 0.00574732 | intron-variant | CHFR | GRCh38.p7 | 12:132856708 | ACACTGCTGGGAGCT[C/T]GCGTGCGCAGTGCTG | 55743 |
rs753235007 | snp | C/T | | | synonymous-codon, intron-variant | CHFR | GRCh38.p7 | 12:132869701 | GAGGTCTGACGTCGA[C/T]GTTGATGGCTGTGGT | 55743 |
rs753235293 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132884581 | AATGGGGCCTGTGAG[C/T]TGATAAATGTTAAAT | 55743 |
rs753244627 | in-del | -/AAA | | | intron-variant | CHFR | GRCh38.p7 | 12:132842109 | GCGAGACTCCATCTC[-/AAA]AAAAAAAAAAAAAAA | 55743 |
rs753265127 | in-del | -/C | 1.6528e-05 | 0.00287467 | intron-variant | CHFR | GRCh38.p7 | 12:132872241 | GCGCCCTCACGTGCA[-/C]CCCCCGTGCGGGTCT | 55743 |
rs753426670 | in-del | -/AA | 0.000181406 | 0.00952208 | intron-variant | CHFR | GRCh38.p7 | 12:132841625 | ATGGCCAAATTACAC[-/AA]GAGAGCATTGGAGAG | 55743 |
rs753427887 | snp | G/T | 1.64738e-05 | 0.00286995 | missense | CHFR | GRCh38.p7 | 12:132872354 | AAGGGCATGTCTGCT[G/T]CTTAACAACCTTCAG | 55743 |
rs753454497 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132855922 | CAGACCCCGGTCTTG[C/T]GCATTAGGAAACCTC | 55743 |
rs753486546 | snp | A/G | 1.82677e-05 | 0.00302217 | intron-variant | CHFR | GRCh38.p7 | 12:132859045 | TGCCATGTTCCGTGA[A/G]CCAAGGGTGAACACG | 55743 |
rs753569472 | snp | A/G | 5.31986e-05 | 0.00515718 | intron-variant | CHFR | GRCh38.p7 | 12:132848229 | CTGCCCGACACTGAG[A/G]ATAAACATATTTCTT | 55743 |
rs753572378 | in-del | -/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132848839 | ATTGTTCAGGAGGGG[-/T]TCTCATGGAAATCGG | 55743 |
rs753670498 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132875207 | AAAACCTACTTCCTA[C/G]TCTTCTATCCCTGAA | 55743 |
rs753721064 | snp | C/T | 1.7483e-05 | 0.00295655 | missense | CHFR | GRCh38.p7 | 12:132853497 | CTCCTGGCTCGCCCT[C/T]GGGTGCTGGGCAGTG | 55743 |
rs753726528 | snp | A/G | | | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132840451 | ATCAAGAGCAAGACA[A/G]CAGTTGAAAACTGTA | 55743 |
rs753746683 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132861730 | AGCCCAGTGCAGCTG[A/G]CAGCCTGAGATGTCG | 55743 |
rs753830316 | snp | A/G | 2.52963e-05 | 0.00355633 | intron-variant | CHFR | GRCh38.p7 | 12:132843123 | TCTATGAGATGTATT[A/G]CACGCACCCACTCAG | 55743 |
rs753847308 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132852535 | GCGAGGTCAACATGC[C/T]GGCCATAAGGACGGC | 55743 |
rs753867941 | snp | C/G | 2.59037e-05 | 0.00359878 | synonymous-codon, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132887257 | CGGCTCGCCCTCCTC[C/G]GCGCCCAGACGCAGG | 55743 |
rs753907430 | snp | A/C | 8.36281e-05 | 0.00646584 | intron-variant | CHFR | GRCh38.p7 | 12:132861442 | CACACGAGAGGACTG[A/C]GGACACACACAACCA | 55743 |
rs753996875 | snp | C/G | | | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132840864 | CCGGTTAGCAAGGAG[C/G]GACTAACTTGGCGGC | 55743 |
rs754006620 | snp | A/G | 5.49209e-05 | 0.00523998 | intron-variant | CHFR | GRCh38.p7 | 12:132842993 | GTAGCTGACGCCTGT[A/G]CCCCCAGCTGCACTC | 55743 |
rs754035414 | snp | A/G | 6.7603e-05 | 0.00581351 | missense | CHFR | GRCh38.p7 | 12:132851651 | GCGGGTCCTGCTCGC[A/G]CTCCGCTCTCCGGTC | 55743 |
rs754094845 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132847662 | GAATGCGCATGTTAA[A/C]CATATGTAAATCCTA | 55743 |
rs754144763 | snp | C/T | 1.68843e-05 | 0.00290549 | missense | CHFR | GRCh38.p7 | 12:132857531 | CCGAGTAGCAAGCCG[C/T]GCAGAACGTGTGCAT | 55743 |
rs754203777 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B | CHFR, LOC101928530 | GRCh38.p7 | 12:132889056 | TCAAGCCTGTAATCC[C/T]AGCACTTTGGGAGGC | 55743 |
rs754257096 | snp | A/G | | | upstream-variant-2KB, intron-variant | CHFR, LOC101928530 | GRCh38.p7 | 12:132888026 | GGTCCGCGAGTGGGA[A/G]CGGCTGCTTGTGGGC | 55743 |
rs754297675 | snp | C/T | 1.64863e-05 | 0.00287104 | missense | CHFR | GRCh38.p7 | 12:132848125 | TTGTTGTTCAGCACG[C/T]CGTCCAGACACTTGT | 55743 |
rs754307363 | snp | A/G | 6.58924e-05 | 0.0057395 | missense | CHFR | GRCh38.p7 | 12:132861526 | TGGGGTTCCAACGAC[A/G]AAAAGGACGCAGTCT | 55743 |
rs754363509 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132852475 | AAGTCTGAGCCCACA[A/C]AGCCAAGTTCCCTGG | 55743 |
rs754422976 | snp | A/G | 0.000279916 | 0.0118271 | intron-variant | CHFR | GRCh38.p7 | 12:132853424 | GCCTGAGGGCGGCGC[A/G]GCTCACCTGTCGTCA | 55743 |
rs754453099 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132851371 | CACAGTGCTGGCAGG[A/G]GATAGACACAGATCC | 55743 |
rs754506935 | snp | C/T | 1.64798e-05 | 0.00287047 | missense | CHFR | GRCh38.p7 | 12:132859150 | TCCCAGCCGCTGCTC[C/T]GACGTCCTCGTGGAC | 55743 |
rs754510547 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132858701 | CCACTGCACTCCAGC[C/G]TGGTGACAGAGCGAG | 55743 |
rs754603143 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132861787 | GAGGAGTGTGTGCTC[A/G]CTCAACTCACATCTT | 55743 |
rs754605513 | snp | C/T | | | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132841166 | TCCTGAAACAATGTT[C/T]TTGATAAACTTGCCC | 55743 |
rs754666879 | snp | A/G | 1.79451e-05 | 0.00299537 | intron-variant | CHFR | GRCh38.p7 | 12:132859051 | GTTCCGTGAGCCAAG[A/G]GTGAACACGGTCGCA | 55743 |
rs754729891 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132872539 | CGTAACGATGCACAC[A/G]TCCACGCACCCCTCA | 55743 |
rs754747845 | snp | C/T | 1.67172e-05 | 0.00289108 | intron-variant | CHFR | GRCh38.p7 | 12:132857386 | GTGCCCGGGTGCTGG[C/T]GTGGATGCCCTCACT | 55743 |
rs754853631 | snp | C/T | 9.53243e-05 | 0.00690312 | synonymous-codon, intron-variant | CHFR | GRCh38.p7 | 12:132869695 | GGGGAAGAGGTCTGA[C/T]GTCGATGTTGATGGC | 55743 |
rs754931883 | snp | C/G | 6.67501e-05 | 0.00577673 | missense | CHFR | GRCh38.p7 | 12:132844098 | CTGCGCAGGCCACAG[C/G]AGTAACACAGAACGG | 55743 |
rs754958760 | snp | A/C | 3.29636e-05 | 0.00405964 | missense | CHFR | GRCh38.p7 | 12:132856470 | GGGCATGATTTACCT[A/C]ATGTCTGAGGACTCA | 55743 |
rs754967879 | snp | G/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132860410 | TACACAATTTTTCAT[G/T]TTTGCTAGAATTAAA | 55743 |
rs754968939 | in-del | -/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132864399 | GCACACTGCCTCACA[-/T]TTAGTAGCTGCTCAA | 55743 |
rs755012453 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132852667 | CAGACAGAGCTGCTG[A/G]GTGGCGGAAGCAAAC | 55743 |
rs755027328 | snp | C/T | 4.94197e-05 | 0.00497066 | synonymous-codon | CHFR | GRCh38.p7 | 12:132861534 | CAACGACGAAAAGGA[C/T]GCAGTCTTTCTGTCT | 55743 |
rs755120503 | snp | C/T | | | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132841076 | TATTAAAATAAAAAA[C/T]AGATAAAATGCTGTG | 55743 |
rs755132431 | snp | C/G | 2.53694e-05 | 0.00356147 | intron-variant | CHFR | GRCh38.p7 | 12:132843001 | CGCCTGTGCCCCCAG[C/G]TGCACTCACATGGCG | 55743 |
rs755177767 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132883451 | AAAAAAAAGACTGGG[C/T]GCAGTGGCTCACGCC | 55743 |
rs755215873 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132855108 | TTAGCTGGGTGTGGT[A/G]GCATATGCCCGTAAT | 55743 |
rs755235847 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132857970 | GTTTGCAGAGTTCAC[A/G]GGGTCACACACGACC | 55743 |
rs755239520 | in-del | -/AAAC | | | intron-variant | CHFR | GRCh38.p7 | 12:132870355 | CGACTCCATCTCAAA[-/AAAC]AAACAAACAAACAAA | 55743 |
rs755285481 | snp | A/G | 4.95103e-05 | 0.00497521 | intron-variant | CHFR | GRCh38.p7 | 12:132872263 | TGCGGGTCTGACCCC[A/G]GCAAGCCTTCCTCTC | 55743 |
rs755292850 | snp | A/T | 1.64789e-05 | 0.0028704 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132841537 | AGTGCTGAAAGCTGC[A/T]CAGGGCCTCTGGATG | 55743 |
rs755310429 | snp | C/T | 1.68741e-05 | 0.00290461 | synonymous-codon | CHFR | GRCh38.p7 | 12:132851655 | GTCCTGCTCGCGCTC[C/T]GCTCTCCGGTCGGGC | 55743 |
rs755355779 | snp | A/C | 2.85923e-05 | 0.00378091 | intron-variant | CHFR | GRCh38.p7 | 12:132848234 | CGACACTGAGGATAA[A/C]CATATTTCTTTTCAT | 55743 |
rs755374387 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132847701 | GGTAGCTTCCTAGAC[A/G]TGGGAAGGCAAATGG | 55743 |
rs755399278 | snp | A/C/T | 3.32128e-05 | 0.00407499 | intron-variant | CHFR | GRCh38.p7 | 12:132870832 | GGCCCCTGTGCAAAC[A/C/T]GAGAACTCATTTTTC | 55743 |
rs755411376 | in-del | -/C | 6.59935e-05 | 0.0057439 | intron-variant | CHFR | GRCh38.p7 | 12:132870696 | AGCTCCTAACATGCA[-/C]CCACTTCTTTGCTAC | 55743 |
rs755463602 | in-del | -/A | | | intron-variant | CHFR | GRCh38.p7 | 12:132847140 | GTAATTCTGTGACGC[-/A]AAAAAAGAGAGGAAT | 55743 |
rs755522022 | snp | C/T | 1.64855e-05 | 0.00287097 | missense | CHFR | GRCh38.p7 | 12:132848126 | TGTTGTTCAGCACGC[C/T]GTCCAGACACTTGTC | 55743 |
rs755554224 | snp | C/T | 1.86308e-05 | 0.00305206 | intron-variant | CHFR | GRCh38.p7 | 12:132859038 | CCTGCAGTGCCATGT[C/T]CCGTGAGCCAAGGGT | 55743 |
rs755612656 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132876247 | TGCATTTATGCAAAA[C/T]ATATATACCAACATA | 55743 |
rs755735109 | in-del | -/ACCTT | | | intron-variant | CHFR | GRCh38.p7 | 12:132843267 | CATGTTTAACTAAAA[-/ACCTT]ACCCAACTGAGGGTC | 55743 |
rs755760659 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132842881 | AAGAGCAGGATTTCT[A/C]AATGAAGATACCGGT | 55743 |
rs755841252 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132855803 | CTTCTTTTTGCTTAA[C/T]AGTCACATGCTAAAC | 55743 |
rs755891788 | snp | A/G | 1.64876e-05 | 0.00287116 | synonymous-codon | CHFR | GRCh38.p7 | 12:132848109 | GTCTGACTCGTAGCT[A/G]TTGTTGTTCAGCACG | 55743 |
rs755970802 | snp | A/G | 1.70664e-05 | 0.00292112 | intron-variant | CHFR | GRCh38.p7 | 12:132843998 | ACCCAGACAGAACTA[A/G]AGCCATGAGGAAGTC | 55743 |
rs756006478 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132878708 | CCTTGTAATCCCAGC[C/T]ACTCAGGAGGATGAG | 55743 |
rs756050840 | snp | C/G/T | 0.000459876 | 0.0151567 | utr-variant-5-prime, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132887332 | GGGCCGCTCCATCGG[C/G/T]ATTCACATCTGCGGA | 55743 |
rs756061068 | snp | A/C/T | 0.000100933 | 0.00710338 | intron-variant | CHFR | GRCh38.p7 | 12:132851760 | ACACGCACATTCAGC[A/C/T]GGAGCACGTGGGACC | 55743 |
rs756088633 | snp | A/C | 1.6708e-05 | 0.00289028 | missense | CHFR | GRCh38.p7 | 12:132859226 | CAGGTCAAGGTCCCC[A/C]TCTACAGGAGAAAGG | 55743 |
rs756135373 | snp | A/G | 1.64784e-05 | 0.00287035 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132841523 | CTCTCTTCACCTCCA[A/G]TGCTGAAAGCTGCTC | 55743 |
rs756160978 | snp | C/T | 1.95421e-05 | 0.00312581 | intron-variant | CHFR | GRCh38.p7 | 12:132877680 | GAGGGTGGGTCAACA[C/T]GGGATATGATCGTGG | 55743 |
rs756165933 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132879921 | TGAATCTGCTTTAGC[C/T]TGAGCCTTGCTCCCA | 55743 |
rs756177652 | snp | C/G | 3.33556e-05 | 0.00408371 | missense | CHFR | GRCh38.p7 | 12:132877610 | CTACAATTCTACAGT[C/G]ATCTCCAGAGACCAG | 55743 |
rs756186305 | in-del | -/CT | 4.94588e-05 | 0.00497262 | intron-variant | CHFR | GRCh38.p7 | 12:132872274 | CCCCGGCAAGCCTTC[-/CT]CTCTCTTACTGTGTT | 55743 |
rs756236953 | snp | A/C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132857103 | TGCTGGTGGAGGGAC[A/C/T]GCCCTCACGTGCCCG | 55743 |
rs756302238 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132868187 | CTCTGAAAACACCAC[A/G]CTAAGTGAAAGAGCC | 55743 |
rs756357861 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132867698 | GGCTCTTCTGTTCAT[A/G]GGAATCTGCAGACTG | 55743 |
rs756361707 | snp | C/T | 1.65083e-05 | 0.00287296 | missense | CHFR | GRCh38.p7 | 12:132857464 | TGGTTTTTACAGATC[C/T]GCTCCACGGGACAGC | 55743 |
rs756428896 | snp | C/T | 6.8313e-05 | 0.00584396 | intron-variant | CHFR | GRCh38.p7 | 12:132848743 | TGGAGAGAGGACACT[C/T]GTTACACGCACTCAG | 55743 |
rs756479695 | snp | A/G | | | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886608 | AACTTTCTCTCACCC[A/G]TTGTATGACTTTGTT | 55743 |
rs756502043 | snp | A/C | 1.64985e-05 | 0.0028721 | intron-variant | CHFR | GRCh38.p7 | 12:132848043 | GGCTGCACTAGGGAG[A/C]AAATGTGGCTCCCGG | 55743 |
rs756512965 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132875332 | AGACCACCTGCCACT[C/T]GCAGCAGATTTAAAA | 55743 |
rs756537119 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132857915 | GAAATACACCTTCCC[A/G]GATAAGGAGCATTTA | 55743 |
rs756631729 | multinucleotide-polymorphism | ACT/GCC | | | intron-variant | CHFR | GRCh38.p7 | 12:132846412 | GGACTACAGGCGCCC[ACT/GCC]ACCACGCCCGGCTAA | 55743 |
rs756661742 | snp | C/G/T | 3.3082e-05 | 0.00406696 | intron-variant | CHFR | GRCh38.p7 | 12:132870820 | CAGAAAAGTGGTGGC[C/G/T]CCTGTGCAAACTGAG | 55743 |
rs756678383 | in-del | -/ATATATAT | | | intron-variant | CHFR | GRCh38.p7 | 12:132850971 | TGTGTGTGCATATAT[-/ATATATAT]ATATATATATATATA | 55743 |
rs756686034 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132847613 | AAGGCCCCACCATTG[C/T]GTGTGCTGTCAGCAA | 55743 |
rs756709185 | snp | A/G | 0.000235097 | 0.0108394 | intron-variant | CHFR | GRCh38.p7 | 12:132861432 | GCCCCAGGAGCACAC[A/G]AGAGGACTGAGGACA | 55743 |
rs756710137 | snp | C/T | | | missense, intron-variant | CHFR | GRCh38.p7 | 12:132869711 | GTCGATGTTGATGGC[C/T]GTGGTTCCTCAAAGC | 55743 |
rs756712256 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132848358 | AAAGATCAGCTCTCC[A/G]AGTCTCCCCAGCACC | 55743 |
rs756736276 | snp | C/G | 3.3054e-05 | 0.00406521 | missense | CHFR | GRCh38.p7 | 12:132857485 | ACGGGACAGCGGCAG[C/G]TAGGACACAGGGACG | 55743 |
rs756778423 | in-del | -/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132867959 | AATAGCTAAGAAAAT[-/T]AAAAAAAAATAATAT | 55743 |
rs756783000 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132864016 | CAATCCACCCACCTC[A/G]GCCTCCCCAAGTGCT | 55743 |
rs756893243 | snp | A/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132854749 | AGGCGGAGCTTGCAA[A/T]GAGCCAAGATCCAGC | 55743 |
rs756917083 | snp | A/G | 1.65149e-05 | 0.00287353 | synonymous-codon | CHFR | GRCh38.p7 | 12:132847071 | CACTCCCCGCTGGAG[A/G]GCCACGAGGCTCTCG | 55743 |
rs756987993 | snp | C/G | 1.65315e-05 | 0.00287498 | intron-variant | CHFR | GRCh38.p7 | 12:132856424 | CACGGTTGTGATGCT[C/G]CTCTGGCTCACACAC | 55743 |
rs757009365 | snp | A/C/G | 8.14289e-05 | 0.00638034 | intron-variant | CHFR | GRCh38.p7 | 12:132877689 | TCAACACGGGATATG[A/C/G]TCGTGGTAACTGTGA | 55743 |
rs757065782 | snp | C/T | 1.97607e-05 | 0.00314324 | missense, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132887321 | TTGCCTTCCTCGGGC[C/T]GCTCCATCGGGATTC | 55743 |
rs757077660 | snp | G/T | 1.67036e-05 | 0.0028899 | synonymous-codon, splice-acceptor-variant | CHFR | GRCh38.p7 | 12:132851736 | CACGTAATCCTGGAC[G/T]GCTGAAGCACACGCA | 55743 |
rs757140926 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132882694 | AGAGGCGTCTCCATG[A/C]CAGAACATCAGGTTT | 55743 |
rs757161863 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132855241 | AGCGAGACTTTGTCT[C/T]GAAAAAAAAAAAAAA | 55743 |
rs757162241 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132860652 | TAATAATCTTAACTT[C/T]GGCTTTCAAAGTGCA | 55743 |
rs757239007 | snp | C/T | 3.34403e-05 | 0.00408889 | missense | CHFR | GRCh38.p7 | 12:132851666 | GCTCCGCTCTCCGGT[C/T]GGGCATGGGCTGGAA | 55743 |
rs757442130 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132879708 | AATACAAAAGCAAGA[A/G]GGAAAATCCTCAATA | 55743 |
rs757444754 | snp | A/C | 1.68872e-05 | 0.00290574 | intron-variant | CHFR | GRCh38.p7 | 12:132857374 | GACCGCCCTCACGTG[A/C]CCGGGTGCTGGTGTG | 55743 |
rs757449626 | in-del | -/TGT | 1.65085e-05 | 0.00287297 | splice-acceptor-variant | CHFR | GRCh38.p7 | 12:132872396 | CTGTTCCACTGGTGC[-/TGT]AAAAAAACAAAAACA | 55743 |
rs757496295 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132866860 | AGCCTGGCCAACAAC[A/G]TCTCTACTAAAAATA | 55743 |
rs757496767 | snp | G/T | 1.97627e-05 | 0.0031434 | missense | CHFR | GRCh38.p7 | 12:132853541 | GCCTGCCTTCTGTAC[G/T]CAGGACACTGCCGGC | 55743 |
rs757695645 | snp | A/C | 4.94344e-05 | 0.00497139 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132841512 | TTAAAAACACGCTCT[A/C]TTCACCTCCAGTGCT | 55743 |
rs757712188 | in-del | -/CCCGGCCCCGGCC | | | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132887170 | TGCCCGGCCCCGGCC[-/CCCGGCCCCGGCC]CCCGGCCCCGGCCTC | 55743 |
rs757715316 | snp | C/T | 1.65957e-05 | 0.00288055 | synonymous-codon | CHFR | GRCh38.p7 | 12:132859211 | CAACAACTGCCCGTT[C/T]AGGTCAAGGTCCCCA | 55743 |
rs757723701 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132856063 | ATAGGACTTTATAGT[C/T]GCTAGATCAACTACA | 55743 |
rs757831785 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132844254 | GACAACGGGCGACAC[A/G]TTAGGAAAATAAGAA | 55743 |
rs757864134 | snp | A/C | 3.30688e-05 | 0.00406612 | intron-variant | CHFR | GRCh38.p7 | 12:132847021 | CATGCGCCTTAGAGC[A/C]GGAGGCAACAGAAGA | 55743 |
rs757876886 | snp | C/T | 6.59174e-05 | 0.00574059 | synonymous-codon | CHFR | GRCh38.p7 | 12:132859169 | GTCCTCGTGGACGGT[C/T]TGGGCATTTCTACGC | 55743 |
rs757969077 | snp | G/T | 9.39629e-05 | 0.00685366 | missense, intron-variant | CHFR | GRCh38.p7 | 12:132869735 | TCAAAGCACACCTGA[G/T]TGGCGGGCGACGACG | 55743 |
rs757973448 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132863907 | GGGACTACAGGTGTG[C/T]ACCACCATGCCCAGC | 55743 |
rs757991138 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132845702 | ATCATACTCCACAAA[A/G]CATCGTGTGCCCCCC | 55743 |
rs758025460 | snp | C/T | 5.07696e-05 | 0.00503808 | missense | CHFR | GRCh38.p7 | 12:132844111 | AGCAGTAACACAGAA[C/T]GGTGTCTCCCGTGAC | 55743 |
rs758029603 | in-del | -/AG | | | intron-variant | CHFR | GRCh38.p7 | 12:132876976 | ATTTTTATATTTTTA[-/AG]AGAGACAGGGTTTCT | 55743 |
rs758084965 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132875035 | GCCCTGATGTAGGCA[A/G]GAAAGCCCAGGACCA | 55743 |
rs758130662 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132853646 | GGTGCAACGCGGGTC[C/T]GCAGCCATCACAGCT | 55743 |
rs758139441 | snp | A/C | 4.96184e-05 | 0.00498063 | missense | CHFR | GRCh38.p7 | 12:132859202 | TTGTGCGACCAACAA[A/C]TGCCCGTTCAGGTCA | 55743 |
rs758214417 | snp | A/G | | | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132841271 | ACTGCCCCTCTCGGC[A/G]GGACGGCCGCATGTT | 55743 |
rs758404229 | snp | A/G | 3.30409e-05 | 0.0040644 | intron-variant | CHFR | GRCh38.p7 | 12:132856709 | CACTGCTGGGAGCTC[A/G]CGTGCGCAGTGCTGC | 55743 |
rs758427205 | in-del | -/CATATATATATATA | | | intron-variant | CHFR | GRCh38.p7 | 12:132850964 | AACTGTATGTGTGTG[-/CATATATATATATA]TATATATATATATAT | 55743 |
rs758453894 | snp | A/C | 0.00011487 | 0.00757771 | intron-variant | CHFR | GRCh38.p7 | 12:132869874 | AGCACACAACCAGGG[A/C]TCAAGCAGACACTCT | 55743 |
rs758454020 | snp | G/T | 1.65814e-05 | 0.00287931 | splice-donor-variant | CHFR | GRCh38.p7 | 12:132857403 | TGGATGCCCTCACTT[G/T]CCTGGATGCTGGATG | 55743 |
rs758622551 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132876753 | ACATCTTCTAATACC[C/T]TGGGAGCCTAATTAA | 55743 |
rs758662673 | snp | A/G | 0.000131781 | 0.00811621 | synonymous-codon | CHFR | GRCh38.p7 | 12:132861537 | CGACGAAAAGGACGC[A/G]GTCTTTCTGTCTGGG | 55743 |
rs758667133 | snp | A/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132847838 | GCTGCGGGAAGCGGC[A/T]CCTACGAATTGGTGG | 55743 |
rs758668795 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132860502 | CCCACACCGATCAAC[C/T]CCACGTGTCAGATAA | 55743 |
rs758776802 | in-del | -/TAAAA | | | intron-variant | CHFR | GRCh38.p7 | 12:132845080 | TTTAAACATCAAAAT[-/TAAAA]TAAAATAAATACAAC | 55743 |
rs758784518 | in-del | -/AC | 1.64762e-05 | 0.00287016 | intron-variant | CHFR | GRCh38.p7 | 12:132844144 | TGTAATCTGGAAGAA[-/AC]ACAGCCAGTTACCCA | 55743 |
rs758817679 | snp | A/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132855926 | CCCCGGTCTTGTGCA[A/T]TAGGAAACCTCAACA | 55743 |
rs758853327 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132865562 | ATTTTCAGTAGAGAC[A/G]GGGTTTCACCATGTT | 55743 |
rs758859251 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132883044 | GAGATGCTTTGTGCT[A/C]AAGTTCTATTCACAG | 55743 |
rs758867711 | snp | A/T | 1.65707e-05 | 0.00287838 | intron-variant | CHFR | GRCh38.p7 | 12:132872404 | CTGGTGCTGTAAAAA[A/T]ACAAAAACACAATTT | 55743 |
rs758918645 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132857756 | TTTTCAGGAAAGACA[C/G]AGGCGAGTAGATTAT | 55743 |
rs758993113 | snp | C/T | 1.72627e-05 | 0.00293786 | intron-variant | CHFR | GRCh38.p7 | 12:132877550 | GAAGCTCAGAACATA[C/T]TCACCTGGTATCTTC | 55743 |
rs758996497 | snp | C/T | 3.29603e-05 | 0.00405944 | missense | CHFR | GRCh38.p7 | 12:132872285 | CTTCCTCTCTCTTAC[C/T]GTGTTCCGGTTCATT | 55743 |
rs759000734 | snp | A/G | 3.90724e-05 | 0.00441981 | intron-variant | CHFR | GRCh38.p7 | 12:132848248 | AACATATTTCTTTTC[A/G]TTACAGATTCTAGAA | 55743 |
rs759076958 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132845173 | AATTAACAAAGATAT[C/T]GGCCAGGCACGGTGG | 55743 |
rs759134793 | snp | G/T | | | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132887095 | ACATTTCACTCCACG[G/T]AAAAATCTGGAGCGC | 55743 |
rs759242088 | snp | A/G | 5.11915e-05 | 0.00505896 | synonymous-codon | CHFR | GRCh38.p7 | 12:132848690 | CCGGGTGCAGCCCCA[A/G]TACAGGTGGCAGAAA | 55743 |
rs759386073 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132864701 | GCCATGTTGGCCAGG[C/T]TGGTCTTGAACTCCC | 55743 |
rs759439729 | snp | C/T | 6.72382e-05 | 0.00579781 | intron-variant | CHFR | GRCh38.p7 | 12:132853600 | CACAGGGCCGAGCTG[C/T]GTGCAGGCCCCAAGC | 55743 |
rs759506585 | in-del | -/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132845694 | GATAAATTATCATAC[-/T]CCACAAAGCATCGTG | 55743 |
rs759529335 | snp | A/G | 0.000269699 | 0.0116093 | synonymous-codon | CHFR | GRCh38.p7 | 12:132853498 | TCCTGGCTCGCCCTC[A/G]GGTGCTGGGCAGTGG | 55743 |
rs759531492 | snp | C/T | 1.69836e-05 | 0.00291402 | intron-variant | CHFR | GRCh38.p7 | 12:132859260 | GTGTTCTGTCGTAAC[C/T]AAGAAGGAAATACAC | 55743 |
rs759599200 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132857774 | GCGAGTAGATTATGA[C/G]TTCAGGAACACAAAC | 55743 |
rs759769869 | snp | A/G | 7.05642e-05 | 0.00593945 | intron-variant | CHFR | GRCh38.p7 | 12:132848621 | GTCAAAGCAACTGGG[A/G]CCTGAAGAGCCAGTA | 55743 |
rs759779899 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132846100 | TGTTTTCATTTCTAC[A/G]TTTGTCCCTTTGTTC | 55743 |
rs759798633 | snp | A/C | 1.672e-05 | 0.00289132 | missense | CHFR | GRCh38.p7 | 12:132859083 | CTCACGCAGTCGTGC[A/C]GCAGGTCCTGGCAGA | 55743 |
rs759805140 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132842675 | ACGGGACGGACGAGA[A/G]CCCAGCTGTGCAGCG | 55743 |
rs759827900 | snp | G/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132877457 | CACTAAAGACAGCAT[G/T]TCTTCTCCTCCTCAG | 55743 |
rs759861639 | in-del | -/ATAA | | | intron-variant | CHFR | GRCh38.p7 | 12:132885423 | TCAAAAAATATATAA[-/ATAA]ATAAATAAATAAATA | 55743 |
rs760055565 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132850214 | CACCTCAGCCTCCCA[A/C]AGGAAATTATTTTTA | 55743 |
rs760238279 | snp | A/G | 3.29451e-05 | 0.00405851 | missense | CHFR | GRCh38.p7 | 12:132856576 | TGCAGCATGTCTTGA[A/G]TGATTTTATTTCTGG | 55743 |
rs760288927 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132879614 | CAGGATGGTCTCGAT[C/G]TCTTGACCTCGTGAT | 55743 |
rs760376738 | snp | C/T | 3.34409e-05 | 0.00408893 | intron-variant | CHFR | GRCh38.p7 | 12:132856742 | AAGGAGGGGTCTGGG[C/T]GGACCGCCCTCACGT | 55743 |
rs760442296 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132854112 | CTCTCCATTTGAAAG[A/G]CTTTTCTGCGCCTCA | 55743 |
rs760466476 | snp | C/T | 3.29554e-05 | 0.00405914 | intron-variant | CHFR | GRCh38.p7 | 12:132856660 | ACACAGCGCCATTCA[C/T]CGGCAGTGAGACATG | 55743 |
rs760476002 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132843693 | GAGTGCTGGCCGAGC[A/G]TGGTGGCTCATGCCT | 55743 |
rs760531565 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132857614 | GATGCAACCGCGACC[A/C]TCGACCAAGGTCCGC | 55743 |
rs760565395 | snp | A/G | | | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886960 | ACGTGACAATATTGC[A/G]TTCTGGAGAGTATAT | 55743 |
rs760584451 | snp | A/G | 4.94931e-05 | 0.00497434 | missense | CHFR | GRCh38.p7 | 12:132859185 | TGGGCATTTCTACGC[A/G]GTTGTGCGACCAACA | 55743 |
rs760617571 | in-del | -/CA | 1.91287e-05 | 0.00309257 | intron-variant | CHFR | GRCh38.p7 | 12:132857585 | AAGAGGAACAGTGTC[-/CA]GACAGTCCCACAGAT | 55743 |
rs760632569 | snp | C/T | 6.00534e-05 | 0.00547934 | intron-variant | CHFR | GRCh38.p7 | 12:132857597 | GTCCAGACAGTCCCA[C/T]AGATGCAACCGCGAC | 55743 |
rs760672251 | snp | C/T | 1.77369e-05 | 0.00297795 | intron-variant | CHFR | GRCh38.p7 | 12:132877539 | AAACACCAAAAGAAG[C/T]TCAGAACATACTCAC | 55743 |
rs760738606 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132873203 | CCGAGTGACCACCAC[A/G]GTTTGCTGAGGGATG | 55743 |
rs760789709 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132853372 | CGTGCACGTCAGCAC[C/T]GGGCACAGCCACAAA | 55743 |
rs760871912 | in-del | -/CCCGGCCCCGGCC | | | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132887158 | AACCCGGTGGCTCTG[-/CCCGGCCCCGGCC]CCCGGCCCCGGCCTC | 55743 |
rs760892631 | snp | C/T | 3.30136e-05 | 0.00406273 | intron-variant | CHFR | GRCh38.p7 | 12:132848074 | CTCCCCAGCCCGCAG[C/T]GAGTCGGTACCTTCA | 55743 |
rs760933260 | snp | A/C | 5.05506e-05 | 0.0050272 | missense | CHFR | GRCh38.p7 | 12:132857528 | AGCCCGAGTAGCAAG[A/C]CGCGCAGAACGTGTG | 55743 |
rs761023052 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132880653 | ACAGAGCAAGACTCC[A/G]ACTCAAAAAAAGAAA | 55743 |
rs761034338 | snp | C/T | 1.66657e-05 | 0.00288662 | missense | CHFR | GRCh38.p7 | 12:132861620 | CTTTAGGGGAGATGC[C/T]ACCACCCCCAGACCC | 55743 |
rs761045629 | snp | C/T | 1.64811e-05 | 0.00287059 | synonymous-codon, intron-variant | CHFR | GRCh38.p7 | 12:132870776 | AGATTCATAGAGGTA[C/T]GCCACGTCTAAAAGA | 55743 |
rs761056185 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132882343 | AAGGCAAAGAAACCA[C/G]ATCAGTGGCTGCCAG | 55743 |
rs761102171 | snp | A/C | 1.6643e-05 | 0.00288465 | synonymous-codon | CHFR | GRCh38.p7 | 12:132851712 | GGCGTGGCTTCCTTG[A/C]AGAGGGCACACGTAA | 55743 |
rs761107024 | snp | A/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132852445 | GGTGCACAAGACCAA[A/T]CGATGTGGCAGCAGA | 55743 |
rs761126986 | snp | A/G | 2.73984e-05 | 0.00370114 | synonymous-codon, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132887236 | CCGCTTCCTCAGGAG[A/G]ACGTGCGGCTCGCCC | 55743 |
rs761156319 | snp | C/T | 2.2034e-05 | 0.00331911 | intron-variant | CHFR | GRCh38.p7 | 12:132843104 | AAAAGAGAAGGGGTA[C/T]GCATCTATGAGATGT | 55743 |
rs761172886 | snp | A/G | 2.8843e-05 | 0.00379745 | intron-variant | CHFR | GRCh38.p7 | 12:132842987 | CACTCTGTAGCTGAC[A/G]CCTGTGCCCCCAGCT | 55743 |
rs761175494 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B | CHFR, LOC101928530 | GRCh38.p7 | 12:132888786 | TGACAAATAGCAGGC[C/T]CTGGAAGAAAACGAA | 55743 |
rs761176081 | snp | C/G | 1.64955e-05 | 0.00287184 | missense | CHFR | GRCh38.p7 | 12:132848090 | GAGTCGGTACCTTCA[C/G]GATGTCTGACTCGTA | 55743 |
rs761182595 | in-del | -/CTTT | | | intron-variant | CHFR | GRCh38.p7 | 12:132860745 | TACCAGGACAGAGGG[-/CTTT]CTTTTTGATTTTCTT | 55743 |
rs761288589 | in-del | -/TA | | | intron-variant | CHFR | GRCh38.p7 | 12:132867959 | AATAGCTAAGAAAAT[-/TA]AAAAAAAATAATATG | 55743 |
rs761297928 | snp | A/G | | | stop-gained, intron-variant | CHFR | GRCh38.p7 | 12:132870736 | TACCAAAGGATTCTT[A/G]TGTCATGCCTTGCTT | 55743 |
rs761337268 | snp | C/G | 1.64727e-05 | 0.00286986 | missense | CHFR | GRCh38.p7 | 12:132856574 | GCTGCAGCATGTCTT[C/G]AGTGATTTTATTTCT | 55743 |
rs761341813 | snp | A/C | | | missense, intron-variant | CHFR | GRCh38.p7 | 12:132869774 | CGGGGATCGGCCCCT[A/C]GCCCTGCACCTGCAC | 55743 |
rs761356222 | snp | A/G | 1.64768e-05 | 0.00287021 | intron-variant | CHFR | GRCh38.p7 | 12:132856652 | TTGAAAGGACACAGC[A/G]CCATTCACCGGCAGT | 55743 |
rs761393257 | in-del | -/CTAA | 3.37211e-05 | 0.00410602 | intron-variant | CHFR | GRCh38.p7 | 12:132859249 | AGAAAGGGATGTGTT[-/CTAA]CTGTCGTAACCAAGA | 55743 |
rs761410378 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132876138 | CCGAGATCGTACCAC[C/T]GCACTTCAGCCTGCA | 55743 |
rs761414901 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132877198 | TTAGATAAATACTCT[C/T]ACCATTGTGTTACAA | 55743 |
rs761444812 | in-del | -/AAAT | 1.64996e-05 | 0.0028722 | intron-variant | CHFR | GRCh38.p7 | 12:132841648 | ATTGGAGAGGCAATC[-/AAAT]AAATTACACAACAGA | 55743 |
rs761464761 | snp | C/T | 9.93295e-05 | 0.00704662 | missense | CHFR | GRCh38.p7 | 12:132843078 | CAGGACGGGATGTTA[C/T]GGCCACTGGAAAAAG | 55743 |
rs761474515 | snp | A/G | 1.65203e-05 | 0.002874 | missense | CHFR | GRCh38.p7 | 12:132859113 | ATGATGCATGTCAGC[A/G]TCTCCTCCATCTTGT | 55743 |
rs761525824 | snp | C/G | 4.96808e-05 | 0.00498377 | missense | CHFR | GRCh38.p7 | 12:132861610 | GGACCACTTCCTTTA[C/G]GGGAGATGCCACCAC | 55743 |
rs761548741 | snp | G/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132856414 | AGCTCTCGGTCACGG[G/T]TGTGATGCTCCTCTG | 55743 |
rs761601993 | snp | G/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132855524 | ACAAAAAAATTAGCT[G/T]GGTGTGGTGGCATGC | 55743 |
rs761606013 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132867096 | ATCCAAAGGAGCCTC[C/T]GAAGAAGGAAGGAGC | 55743 |
rs761615752 | snp | A/C | 1.64735e-05 | 0.00286993 | missense | CHFR | GRCh38.p7 | 12:132861510 | CAAATCCTCCTGATC[A/C]TGGGGTTCCAACGAC | 55743 |
rs761621204 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132842838 | GTGGAAGACGGAGAT[A/C]AAACTGCATGAAACG | 55743 |
rs761633567 | snp | C/G | 1.64738e-05 | 0.00286995 | missense | CHFR | GRCh38.p7 | 12:132872313 | ATTCTTCCTGTACAC[C/G]AAGTAGATGACATCC | 55743 |
rs761685860 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132849664 | ATAGTGGAGCAATCT[C/T]GGCTCACTGCAACCT | 55743 |
rs761783455 | snp | G/T | | | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132885957 | GATATCTAAATACTT[G/T]CAAAGTTGTAAAATA | 55743 |
rs761784455 | snp | C/G | 1.91027e-05 | 0.00309047 | intron-variant | CHFR | GRCh38.p7 | 12:132859023 | ACACGGGACGAAGAA[C/G]CTGCAGTGCCATGTT | 55743 |
rs761785423 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132872039 | GTTTCTCCTTGGCTG[C/T]CATTTTGGGATTGGC | 55743 |
rs761908114 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132883955 | AAACCTCATCTCTAC[C/T]AAAAATACCAAAAAA | 55743 |
rs762075096 | in-del | -/CTT | | | intron-variant | CHFR | GRCh38.p7 | 12:132855788 | AGTGGTTTTGGTTTC[-/CTT]CTTTTTGCTTAACAG | 55743 |
rs762099651 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132853153 | CTGCCCTGAGGCAGT[A/G]GCTGGGGAGAGGCCA | 55743 |
rs762107788 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132880573 | TGAGGCAGAAGAATG[A/G]CGTGAACCCAGGAGG | 55743 |
rs762113571 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132876378 | CTTTTTGAGCACCAA[A/C]AAGACACTCAAAAAA | 55743 |
rs762200320 | snp | A/G | 0.000487567 | 0.015606 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132887187 | CCGGCCCCGGCCTCA[A/G]CCCCGCACCTCGTCT | 55743 |
rs762267676 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132868056 | AACAGAAAACATTCC[C/T]GTCACGCTGCACCCA | 55743 |
rs762287710 | snp | A/G | 6.66867e-05 | 0.00577398 | missense | CHFR | GRCh38.p7 | 12:132857518 | CGCTCCATCCAGCCC[A/G]AGTAGCAAGCCGCGC | 55743 |
rs762328534 | snp | A/C | 0.00243902 | 0.0348362 | intron-variant | CHFR | GRCh38.p7 | 12:132853611 | GCTGTGTGCAGGCCC[A/C]AAGCCTCTCAGGTAG | 55743 |
rs762370690 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132869909 | ATTGAAATGCTCTTA[A/G]GAATGCAACAGCCCC | 55743 |
rs762481129 | snp | A/G | 1.64787e-05 | 0.00287038 | missense | CHFR | GRCh38.p7 | 12:132861490 | ATTTTCTTCTTCACG[A/G]GCTCCAAATCCTCCT | 55743 |
rs762512468 | snp | A/C | 1.64931e-05 | 0.00287163 | intron-variant | CHFR | GRCh38.p7 | 12:132841630 | CAAATTACACAAGAG[A/C]GCATTGGAGAGGCAA | 55743 |
rs762524769 | in-del | -/G | 1.64735e-05 | 0.00286993 | frameshift-variant | CHFR | GRCh38.p7 | 12:132861512 | AATCCTCCTGATCCT[-/G]GGGTTCCAACGACGA | 55743 |
rs762533647 | in-del | -/A | | | intron-variant | CHFR | GRCh38.p7 | 12:132863411 | TTGGGAGGCTGAGGC[-/A]AGGAGAACTGCTTGA | 55743 |
rs762553767 | snp | C/G | | | upstream-variant-2KB, nc-transcript-variant | CHFR, LOC101928530 | GRCh38.p7 | 12:132888534 | TATAGGCATAGTTAT[C/G]TATACCTTGTAAACC | 55743 |
rs762580704 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132875912 | GGGCGCGATGGCTCA[C/T]GCCTGTAATCCCAGC | 55743 |
rs762628104 | in-del | -/CCCCGGC | 0.000439464 | 0.0148168 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132887162 | GGTGGCTCTGCCCGG[-/CCCCGGC]CCCCGGCCCCCGGCC | 55743 |
rs762683133 | snp | C/T | 1.64787e-05 | 0.00287038 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132841506 | TGTATTTTAAAAACA[C/T]GCTCTCTTCACCTCC | 55743 |
rs762743160 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132882654 | ACCAGTGCAAGTCAC[A/G]GTGTCGCCAGAGCCA | 55743 |
rs762757157 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132854648 | AGTCTCTACCAAAAA[C/T]ACAAAAAATTAGCCG | 55743 |
rs762757910 | snp | A/C | 1.76201e-05 | 0.00296812 | missense | CHFR | GRCh38.p7 | 12:132877651 | GGGAAGGAAAGGTCG[A/C]AACCTAAAAAAGAGA | 55743 |
rs762824545 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132860209 | GTTATCATGGTACAT[C/T]TGATTTATCAATTTT | 55743 |
rs762831160 | snp | C/T | 0.00036354 | 0.0134773 | intron-variant | CHFR | GRCh38.p7 | 12:132870813 | ATCAAATCAGAAAAG[C/T]GGTGGCCCCTGTGCA | 55743 |
rs762889948 | snp | A/G | 1.66821e-05 | 0.00288804 | intron-variant | CHFR | GRCh38.p7 | 12:132847152 | CGCAAAAAAAGAGAG[A/G]AATAAGAAATACTCG | 55743 |
rs762941953 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132854960 | AAATACAAAATTAGC[A/G]GCCGGGCGCGGTGGC | 55743 |
rs762960295 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132842811 | AGCTACTCCAGCCAG[A/G]AAGACACAGAAGTGG | 55743 |
rs762961678 | snp | C/T | 1.64727e-05 | 0.00286986 | missense | CHFR | GRCh38.p7 | 12:132856549 | TCAGAAAAAGACCGC[C/T]TGACTTTGGGCTGCA | 55743 |
rs763051669 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132843490 | AATAAAATTACCCCA[C/G]TTGACTATTGGATGT | 55743 |
rs763156029 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132861412 | CATGGCAGCGGCCCC[C/T]GCATGCCCCAGGAGC | 55743 |
rs763257394 | snp | A/T | | | missense | CHFR | GRCh38.p7 | 12:132851687 | TGGGCTGGAAGCAGC[A/T]GGTGCACAGGGCGTG | 55743 |
rs763278073 | snp | C/T | 0.000194373 | 0.0098564 | intron-variant | CHFR | GRCh38.p7 | 12:132853418 | GCTGAGGCCTGAGGG[C/T]GGCGCGGCTCACCTG | 55743 |
rs763284864 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132871811 | GTGACCTTCGAAGGA[C/T]TCCCATAACTTTCCT | 55743 |
rs763318128 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132850381 | TGCTCTGTGAAATTA[A/G]AGTGAAGAGTTTGGA | 55743 |
rs763326795 | snp | C/G | 0.000234596 | 0.0108279 | intron-variant | CHFR | GRCh38.p7 | 12:132851569 | TTTGAAACCTGACCC[C/G]TGAAGGACAGATAGG | 55743 |
rs763356188 | snp | C/T | 1.6701e-05 | 0.00288968 | missense | CHFR | GRCh38.p7 | 12:132877576 | TCTTCCAGTGTCACC[C/T]GACCTGATTTTTCAT | 55743 |
rs763483345 | in-del | -/TCT | | | intron-variant | CHFR | GRCh38.p7 | 12:132846262 | GTTCATGCTTAACTG[-/TCT]TTTTTTTTTTTTTTT | 55743 |
rs763498728 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon | CHFR | GRCh38.p7 | 12:132856560 | CCGCCTGACTTTGGG[C/T]TGCAGCATGTCTTGA | 55743 |
rs763509451 | snp | C/T | 1.69306e-05 | 0.00290947 | intron-variant | CHFR | GRCh38.p7 | 12:132857370 | GAGGGACCGCCCTCA[C/T]GTGCCCGGGTGCTGG | 55743 |
rs763536897 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132867392 | CAGAGGGAGCAGTCT[C/T]CTGGGAGACATGGCT | 55743 |
rs763538909 | snp | A/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132880453 | CACAAGGTCAGGAGA[A/T]CGAGACCATCCTGGC | 55743 |
rs763544252 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132864310 | CCGGCACCCACTCAC[A/G]CCATCATCTCCAGCG | 55743 |
rs763562338 | snp | G/T | | | upstream-variant-2KB, nc-transcript-variant | CHFR, LOC101928530 | GRCh38.p7 | 12:132887854 | ACTTCCGGATTGGAA[G/T]CCCCAAGGATTCTGA | 55743 |
rs763567811 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132856078 | CGCTAGATCAACTAC[A/G]AAGAATACATGTGCT | 55743 |
rs763578887 | snp | C/T | 3.3583e-05 | 0.0040976 | intron-variant | CHFR | GRCh38.p7 | 12:132847166 | GGAATAAGAAATACT[C/T]GTTTAGAGGAAGAAA | 55743 |
rs763591670 | snp | G/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132879652 | CCTCGGCTTCTCAAA[G/T]TGCTGGGATTACAGG | 55743 |
rs763682576 | in-del | -/AG | | | intron-variant | CHFR | GRCh38.p7 | 12:132863707 | CACGAGCAAGAAGCC[-/AG]AGTCATAACGACAGG | 55743 |
rs763689050 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132864811 | TTTTTTTTTAATTAC[A/G]TAAGTAATATATAAA | 55743 |
rs763748376 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132863926 | ACCATGCCCAGCTAA[A/G]TTGTTTTTTGTATTT | 55743 |
rs763759331 | snp | A/G/T | 1.98695e-05 | 0.00315188 | intron-variant | CHFR | GRCh38.p7 | 12:132877684 | GTGGGTCAACACGGG[A/G/T]TATGATCGTGGTAAC | 55743 |
rs763767876 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132854662 | ATACAAAAAATTAGC[C/T]GGGCATGGTATCGGG | 55743 |
rs763886708 | in-del | -/TT/TTT | | | intron-variant | CHFR | GRCh38.p7 | 12:132846265 | ATGCTTAACTGTCTT[-/TT/TTT]TTTTTTTTTTTTTTT | 55743 |
rs763959401 | snp | A/G | 1.65236e-05 | 0.00287429 | intron-variant | CHFR | GRCh38.p7 | 12:132872247 | CTCACGTGCACCCCC[A/G]TGCGGGTCTGACCCC | 55743 |
rs764048451 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132871837 | TTCCTTGTCCTATAC[C/T]GTTCTTCCACAAAAC | 55743 |
rs764155374 | snp | A/G | 8.45459e-05 | 0.00650121 | intron-variant | CHFR | GRCh38.p7 | 12:132857371 | AGGGACCGCCCTCAC[A/G]TGCCCGGGTGCTGGT | 55743 |
rs764189832 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132875913 | GGCGCGATGGCTCAC[A/G]CCTGTAATCCCAGCA | 55743 |
rs764201655 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132860515 | ACCCCACGTGTCAGA[C/T]AACCTAATTTCTTTC | 55743 |
rs764257940 | snp | A/C | 1.77303e-05 | 0.00297739 | intron-variant | CHFR | GRCh38.p7 | 12:132861653 | TGAGAGGAATCAAAC[A/C]AGATAGGTGCTGATC | 55743 |
rs764279540 | snp | C/T | 6.59228e-05 | 0.00574083 | synonymous-codon | CHFR | GRCh38.p7 | 12:132861486 | TCTCATTTTCTTCTT[C/T]ACGGGCTCCAAATCC | 55743 |
rs764304023 | snp | C/T | | | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132840586 | TTATTCCAGATGACA[C/T]GGCAAAGCTAGCACA | 55743 |
rs764423128 | snp | C/G | | | missense | CHFR | GRCh38.p7 | 12:132851717 | GGCTTCCTTGCAGAG[C/G]GCACACGTAATCCTG | 55743 |
rs764448295 | snp | A/G | 3.3123e-05 | 0.00406945 | missense | CHFR | GRCh38.p7 | 12:132844068 | TGCCGATACTGATAG[A/G]TCAGCTCACGGAAGC | 55743 |
rs764464430 | in-del | -/TG | | | intron-variant | CHFR | GRCh38.p7 | 12:132842316 | ATTTCTACTGAAAAC[-/TG]TCTGCCAGTCAACAG | 55743 |
rs764510225 | in-del | -/AA | | | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886376 | GGGTGAAATTAACCA[-/AA]AAAAAAAAAAAAATT | 55743 |
rs764514074 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132879677 | TACAGGCGTGAGCCA[C/G]CAGCGCCCGGCCCTG | 55743 |
rs764607751 | snp | C/T | 1.66732e-05 | 0.00288727 | missense | CHFR | GRCh38.p7 | 12:132877580 | CCAGTGTCACCTGAC[C/T]TGATTTTTCATCCAC | 55743 |
rs764629991 | snp | C/T | 1.65051e-05 | 0.00287267 | missense | CHFR | GRCh38.p7 | 12:132857437 | TATGCTTCCACGAGG[C/T]TGTTGAGGATGTGGT | 55743 |
rs764651869 | snp | A/G | 1.70464e-05 | 0.0029194 | intron-variant | CHFR | GRCh38.p7 | 12:132859266 | TGTCGTAACCAAGAA[A/G]GAAATACACGCAGGT | 55743 |
rs764710128 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132851321 | AGCATCAACATTCAT[A/G]TAAGAGGTTTAACAG | 55743 |
rs764717212 | snp | A/G | | | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886221 | GAGGCTGAGGCGGGA[A/G]AATCACTTGAACCGG | 55743 |
rs764723102 | snp | A/G | 1.79741e-05 | 0.00299779 | synonymous-codon | CHFR | GRCh38.p7 | 12:132853510 | CTCGGGTGCTGGGCA[A/G]TGGGGAGGCTGCGCC | 55743 |
rs764757412 | snp | C/T | 6.59207e-05 | 0.00574073 | missense | CHFR | GRCh38.p7 | 12:132859153 | CAGCCGCTGCTCTGA[C/T]GTCCTCGTGGACGGT | 55743 |
rs764779443 | in-del | -/A | | | intron-variant | CHFR | GRCh38.p7 | 12:132854331 | GATCGGTGTCTGGAT[-/A]AACAAACTTATCAAA | 55743 |
rs764814472 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132857778 | GTAGATTATGACTTC[A/G]GGAACACAAACAACA | 55743 |
rs764877035 | snp | A/T | | | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132887096 | CATTTCACTCCACGG[A/T]AAAATCTGGAGCGCA | 55743 |
rs764890493 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132858083 | AAGTGGTAGCCATGC[A/G]GGGTGGCTCACGTCT | 55743 |
rs764905392 | snp | C/G | 5.10495e-05 | 0.00505194 | synonymous-codon | CHFR | GRCh38.p7 | 12:132877557 | AGAACATACTCACCT[C/G]GTATCTTCCAGTGTC | 55743 |
rs764906226 | in-del | -/T | 1.69427e-05 | 0.00291051 | intron-variant | CHFR | GRCh38.p7 | 12:132859255 | GGATGTGTTCTGTCG[-/T]TAACCAAGAAGGAAA | 55743 |
rs764906572 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132863728 | ATAACGACAGGAATG[A/C]CCTTGGCAGAAAAAC | 55743 |
rs764944213 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132873386 | AACCAGGCAGTGGCT[A/G]TGTGTGTCTGAGTTC | 55743 |
rs764961378 | in-del | -/G | 3.00386e-05 | 0.00387536 | intron-variant | CHFR | GRCh38.p7 | 12:132842980 | ATTCATCACTCTGTA[-/G]GCTGACGCCTGTGCC | 55743 |
rs764979750 | in-del | -/TTTC | | | intron-variant | CHFR | GRCh38.p7 | 12:132860758 | GGCTTTCTTTTTGAT[-/TTTC]TTTTTTTTGAGATGG | 55743 |
rs765047882 | snp | A/G | 6.64011e-05 | 0.00576161 | intron-variant | CHFR | GRCh38.p7 | 12:132847138 | AGGTAATTCTGTGAC[A/G]CAAAAAAAGAGAGGA | 55743 |
rs765096474 | snp | C/T | 4.94474e-05 | 0.00497205 | missense, intron-variant | CHFR | GRCh38.p7 | 12:132870781 | CATAGAGGTATGCCA[C/T]GTCTAAAAGAAAATC | 55743 |
rs765151194 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132854435 | GCATGTGCACAAATA[C/T]GGATGGAAGAAATGC | 55743 |
rs765179199 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132873156 | CTCTGCAGCTTCACT[C/G]CCGAGGCCCCAGCAG | 55743 |
rs765182247 | snp | A/G | 0.00010836 | 0.00735991 | intron-variant | CHFR | GRCh38.p7 | 12:132869854 | AACCCAAAAGGAGCA[A/G]AAGCAGCACACAACC | 55743 |
rs765209251 | snp | C/T | 1.65375e-05 | 0.0028755 | intron-variant | CHFR | GRCh38.p7 | 12:132847012 | GGACACTCACATGCG[C/T]CTTAGAGCAGGAGGC | 55743 |
rs765209279 | snp | C/G | 7.00599e-05 | 0.0059182 | intron-variant | CHFR | GRCh38.p7 | 12:132853607 | CCGAGCTGTGTGCAG[C/G]CCCCAAGCCTCTCAG | 55743 |
rs765230312 | snp | G/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132882615 | GAGCGTTAACTGCCA[G/T]GACAGTCTCCTTCAA | 55743 |
rs765254956 | snp | C/T | 5.45777e-05 | 0.00522359 | intron-variant | CHFR | GRCh38.p7 | 12:132843131 | ATGTATTGCACGCAC[C/T]CACTCAGCTACCTGA | 55743 |
rs765292975 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132870110 | GTAATCCCAGCACTT[C/T]GGGAGGCTGAGGCGG | 55743 |
rs765399506 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132860302 | CATTACATTAACAGA[C/T]TACATTAGTTCATGA | 55743 |
rs765505226 | snp | A/G | 0.000707772 | 0.0187985 | missense | CHFR | GRCh38.p7 | 12:132848707 | ACAGGTGGCAGAAAG[A/G]CTGCAGGCAGACCGC | 55743 |
rs765605647 | snp | C/T | 1.66813e-05 | 0.00288797 | missense | CHFR | GRCh38.p7 | 12:132851731 | GGGCACACGTAATCC[C/T]GGACTGCTGAAGCAC | 55743 |
rs765611625 | snp | A/G | 5.61372e-05 | 0.00529768 | synonymous-codon | CHFR | GRCh38.p7 | 12:132848663 | CGGGGCCAGGCAGCC[A/G]TAGCAGCCGGTCCGG | 55743 |
rs765687815 | snp | C/T | 5.31561e-05 | 0.00515512 | missense, intron-variant | CHFR | GRCh38.p7 | 12:132869633 | CCACAACTGGAGGAA[C/T]GCTCTCGCCCTGCAG | 55743 |
rs765727915 | snp | A/G | 9.89723e-05 | 0.00703394 | intron-variant | CHFR | GRCh38.p7 | 12:132856695 | GCAGACACAGCTCAC[A/G]CTGCTGGGAGCTCGC | 55743 |
rs765839818 | snp | C/G | | | missense | CHFR | GRCh38.p7 | 12:132877637 | CCAGTTTATTGCTGG[C/G]GAAGGAAAGGTCGCA | 55743 |
rs765845584 | snp | C/T | 1.64808e-05 | 0.00287057 | synonymous-codon | CHFR | GRCh38.p7 | 12:132859145 | TGGCTTCCCAGCCGC[C/T]GCTCTGACGTCCTCG | 55743 |
rs765917829 | in-del | -/GCG | 2.24595e-05 | 0.00335101 | cds-indel, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132887288 | GCCGTCCCCAGGGCT[-/GCG]GCGGCGGCGGCGACT | 55743 |
rs765931951 | snp | A/G | 1.64738e-05 | 0.00286995 | stop-gained | CHFR | GRCh38.p7 | 12:132872351 | GTAAAGGGCATGTCT[A/G]CTTCTTAACAACCTT | 55743 |
rs765947992 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132843787 | AACCCCGTCTCTACT[A/G]AAACACAAAAAATTA | 55743 |
rs765974987 | snp | A/C/T | 3.30198e-05 | 0.00406313 | intron-variant | CHFR | GRCh38.p7 | 12:132872259 | CCCGTGCGGGTCTGA[A/C/T]CCCGGCAAGCCTTCC | 55743 |
rs765980391 | in-del | -/CTCTATA | | | intron-variant | CHFR | GRCh38.p7 | 12:132842067 | CAGCTGAGATCACAC[-/CTCTATA]CTCTATACTCCAGCC | 55743 |
rs766020195 | snp | A/G | 5.04096e-05 | 0.00502018 | missense | CHFR | GRCh38.p7 | 12:132848679 | TAGCAGCCGGTCCGG[A/G]TGCAGCCCCAGTACA | 55743 |
rs766084372 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132884525 | TACCCCCCTAAAATT[C/T]ATATATTTAAGTCCT | 55743 |
rs766086284 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132873231 | ATGGGAGTGGCAAAC[A/G]ATTTCCATAAACAGA | 55743 |
rs766096241 | snp | C/T | 1.65971e-05 | 0.00288067 | missense | CHFR | GRCh38.p7 | 12:132844083 | GTCAGCTCACGGAAG[C/T]TGCGCAGGCCACAGC | 55743 |
rs766185512 | snp | C/T | 1.65395e-05 | 0.00287567 | intron-variant | CHFR | GRCh38.p7 | 12:132847002 | GCACAGCCCTGGACA[C/T]TCACATGCGCCTTAG | 55743 |
rs766186786 | snp | A/G | 0.000117202 | 0.00765422 | intron-variant | CHFR | GRCh38.p7 | 12:132848220 | AAGCACTGTCTGCCC[A/G]ACACTGAGGATAAAC | 55743 |
rs766363905 | snp | C/T | 0.000113411 | 0.00752945 | intron-variant | CHFR | GRCh38.p7 | 12:132842989 | CTCTGTAGCTGACGC[C/T]TGTGCCCCCAGCTGC | 55743 |
rs766376169 | snp | A/G | 3.38593e-05 | 0.00411443 | synonymous-codon | CHFR | GRCh38.p7 | 12:132851649 | ACGCGGGTCCTGCTC[A/G]CGCTCCGCTCTCCGG | 55743 |
rs766380871 | snp | A/C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132852441 | CCACGGTGCACAAGA[A/C/T]CAATCGATGTGGCAG | 55743 |
rs766434355 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132862464 | AAAAAATTAACTAGG[A/C]GTGACAGTACGAGCA | 55743 |
rs766435334 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132880858 | TAATCCCAGCTACAC[A/G]GGAGGCTAAGGCAGG | 55743 |
rs766461060 | snp | C/G | 0.000594943 | 0.0172371 | missense, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132887244 | TCAGGAGGACGTGCG[C/G]CTCGCCCTCCTCCGC | 55743 |
rs766469365 | snp | A/G | 1.66449e-05 | 0.00288482 | synonymous-codon | CHFR | GRCh38.p7 | 12:132851714 | CGTGGCTTCCTTGCA[A/G]AGGGCACACGTAATC | 55743 |
rs766543527 | snp | C/G/T | 5.01065e-05 | 0.00500507 | intron-variant | CHFR | GRCh38.p7 | 12:132853396 | CCACAAAGTGACTCA[C/G/T]GCGAAGGCTGAGGCC | 55743 |
rs766575351 | snp | A/G | | | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132840851 | CCGCGGTCACTCACC[A/G]GTTAGCAAGGAGCGA | 55743 |
rs766576148 | snp | G/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132863278 | TTCAGGAGGCCAAGG[G/T]GGGTGGATCATCTGA | 55743 |
rs766589059 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132881738 | CCGGGCATGGTGGCA[C/T]GTGCCTGTAGTCCCA | 55743 |
rs766660009 | snp | C/T | 5.05966e-05 | 0.00502949 | synonymous-codon | CHFR | GRCh38.p7 | 12:132857529 | GCCCGAGTAGCAAGC[C/T]GCGCAGAACGTGTGC | 55743 |
rs766667278 | snp | C/G | 1.6717e-05 | 0.00289106 | missense | CHFR | GRCh38.p7 | 12:132861623 | TAGGGGAGATGCCAC[C/G]ACCCCCAGACCCTGT | 55743 |
rs766718829 | in-del | -/A | 1.64732e-05 | 0.0028699 | frameshift-variant | CHFR | GRCh38.p7 | 12:132861520 | TGATCCTGGGGTTCC[-/A]ACGACGAAAAGGACG | 55743 |
rs766728386 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132848464 | AAGGCTTGATTTTGA[A/G]CTAACACGAATTTGA | 55743 |
rs766728846 | snp | A/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132867030 | CAGAGCAAGACTCTG[A/T]CTCAAAAAAACAGAA | 55743 |
rs766865645 | snp | C/G | 1.64727e-05 | 0.00286986 | missense | CHFR | GRCh38.p7 | 12:132856588 | TGAGTGATTTTATTT[C/G]TGGCATCCATACTTT | 55743 |
rs766901024 | snp | G/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132860411 | ACACAATTTTTCATG[G/T]TTGCTAGAATTAAAA | 55743 |
rs766927581 | snp | C/T | 6.02476e-05 | 0.00548819 | intron-variant | CHFR | GRCh38.p7 | 12:132848211 | GTCGCAGGAAAGCAC[C/T]GTCTGCCCGACACTG | 55743 |
rs766957926 | snp | A/G | 4.45742e-05 | 0.00472071 | intron-variant | CHFR | GRCh38.p7 | 12:132843105 | AAAGAGAAGGGGTAC[A/G]CATCTATGAGATGTA | 55743 |
rs767022889 | snp | C/G | | | upstream-variant-2KB, downstream-variant-500B | CHFR, LOC101928530 | GRCh38.p7 | 12:132888851 | TTTTACGTAGCCCTG[C/G]AAAACTGTCTCCTGG | 55743 |
rs767051971 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132877252 | AGCACGCTGTATAGG[C/T]TGATAGCCTAGGAGC | 55743 |
rs767082498 | snp | C/T | 1.64917e-05 | 0.00287151 | synonymous-codon | CHFR | GRCh38.p7 | 12:132848100 | CTTCAGGATGTCTGA[C/T]TCGTAGCTGTTGTTG | 55743 |
rs767140702 | snp | C/T | | | missense | CHFR | GRCh38.p7 | 12:132848664 | GGGGCCAGGCAGCCG[C/T]AGCAGCCGGTCCGGG | 55743 |
rs767254938 | in-del | -/GCCCCTGCACTAACTCGGGACCTCCCCTTCTCAGCCTT | | | downstream-variant-500B | CHFR | GRCh38.p7 | 12:132839934 | CTCCCCCTTAGCCTC[lengthTooLong]GCCCCTGCACTAACT | 55743 |
rs767279680 | snp | C/T | 1.65241e-05 | 0.00287433 | intron-variant | CHFR | GRCh38.p7 | 12:132856426 | CGGTTGTGATGCTCC[C/T]CTGGCTCACACACTC | 55743 |
rs767308125 | snp | C/G | 5.71772e-05 | 0.00534652 | intron-variant | CHFR | GRCh38.p7 | 12:132859024 | CACGGGACGAAGAAC[C/G]TGCAGTGCCATGTTC | 55743 |
rs767325947 | snp | A/C/G | 0.000191118 | 0.00977391 | intron-variant | CHFR | GRCh38.p7 | 12:132853419 | CTGAGGCCTGAGGGC[A/C/G]GCGCGGCTCACCTGT | 55743 |
rs767348322 | snp | A/T | 1.65031e-05 | 0.00287251 | missense | CHFR | GRCh38.p7 | 12:132859123 | TCAGCGTCTCCTCCA[A/T]CTTGTCTGGCTTCCC | 55743 |
rs767392115 | snp | A/C | 1.64738e-05 | 0.00286995 | missense | CHFR | GRCh38.p7 | 12:132872315 | TCTTCCTGTACACCA[A/C]GTAGATGACATCCCC | 55743 |
rs767476620 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132842825 | GGAAGACACAGAAGT[A/G]GAAGACGGAGATAAA | 55743 |
rs767493226 | snp | A/G | | | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886089 | GGCCGAAGCAGGTGA[A/G]TCACTTTAGTTCAGT | 55743 |
rs767497782 | snp | C/T | 4.95103e-05 | 0.00497521 | missense | CHFR | GRCh38.p7 | 12:132857455 | TTGAGGATGTGGTTT[C/T]TACAGATCCGCTCCA | 55743 |
rs767510795 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132843672 | ACAGGGTGTCTGTAA[A/C]GAAAAGAGTGCTGGC | 55743 |
rs767524437 | in-del | -/AAAA | | | intron-variant | CHFR | GRCh38.p7 | 12:132881868 | GCAAGACGCTGTCTC[-/AAAA]AAAAAAAAAAAAAAA | 55743 |
rs767567997 | snp | C/T | 1.79845e-05 | 0.00299865 | intron-variant | CHFR | GRCh38.p7 | 12:132851589 | GGACAGATAGGAACC[C/T]GCCTGCGTGCGGTGG | 55743 |
rs767568711 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132872060 | TGGGATTGGCTGCTC[A/G]TGGCCACAGTGGTAT | 55743 |
rs767575276 | in-del | -/AAA | | | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886375 | GGGGTGAAATTAACC[-/AAA]AAAAAAAAAAAAATT | 55743 |
rs767585723 | snp | C/T | 9.84397e-05 | 0.007015 | missense, intron-variant | CHFR | GRCh38.p7 | 12:132869822 | CCATGGAACACATTT[C/T]CCTTGTTAGCTTCTG | 55743 |
rs767607801 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132850704 | CCATTCCAGACAGAA[C/G]CAGTGCTGTGGTCCT | 55743 |
rs767634272 | snp | A/G | 1.6715e-05 | 0.00289089 | synonymous-codon | CHFR | GRCh38.p7 | 12:132857520 | CTCCATCCAGCCCGA[A/G]TAGCAAGCCGCGCAG | 55743 |
rs767637232 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132879719 | AAGAGGGAAAATCCT[C/G]AATACTTGCCCTCTC | 55743 |
rs767887460 | snp | C/T | 3.05031e-05 | 0.00390521 | intron-variant | CHFR | GRCh38.p7 | 12:132842974 | TTAACTCATTCATCA[C/T]TCTGTAGCTGACGCC | 55743 |
rs767923691 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132869936 | CCCCAAGGCCAGGCA[C/T]GGTGGTGCAGGCCTG | 55743 |
rs767988129 | snp | C/T | 1.64732e-05 | 0.0028699 | synonymous-codon | CHFR | GRCh38.p7 | 12:132861522 | ATCCTGGGGTTCCAA[C/T]GACGAAAAGGACGCA | 55743 |
rs767989797 | in-del | -/AATC | 1.64966e-05 | 0.00287194 | intron-variant | CHFR | GRCh38.p7 | 12:132870793 | CCACGTCTAAAAGAA[-/AATC]AATCAAATCAGAAAA | 55743 |
rs768006499 | snp | A/C | 1.6865e-05 | 0.00290383 | intron-variant | CHFR | GRCh38.p7 | 12:132861418 | AGCGGCCCCCGCATG[A/C]CCCAGGAGCACACGA | 55743 |
rs768008453 | in-del | -/ATATATATAT | | | intron-variant | CHFR | GRCh38.p7 | 12:132850969 | TATGTGTGTGCATAT[-/ATATATATAT]ATATATATATATATA | 55743 |
rs768027408 | snp | A/G | 1.86614e-05 | 0.00305456 | intron-variant | CHFR | GRCh38.p7 | 12:132877668 | ACCTAAAAAAGAGAG[A/G]GTGGGTCAACACGGG | 55743 |
rs768052255 | snp | C/T | 1.64784e-05 | 0.00287035 | synonymous-codon | CHFR | GRCh38.p7 | 12:132861492 | TTTCTTCTTCACGGG[C/T]TCCAAATCCTCCTGA | 55743 |
rs768065335 | snp | A/G | 1.70197e-05 | 0.00291711 | missense | CHFR | GRCh38.p7 | 12:132851638 | TGAGGGGCGACACGC[A/G]GGTCCTGCTCGCGCT | 55743 |
rs768078789 | snp | A/G | 3.82066e-05 | 0.00437056 | synonymous-codon | CHFR | GRCh38.p7 | 12:132843055 | GCAGTTACGGCCCCA[A/G]TAGCAGTCAGGACGG | 55743 |
rs768101973 | snp | A/G | | | upstream-variant-2KB, intron-variant | CHFR, LOC101928530 | GRCh38.p7 | 12:132887997 | ACAGATCCGAAGTCT[A/G]AGGCACAGGGCGCGG | 55743 |
rs768149842 | snp | A/G | 1.68755e-05 | 0.00290473 | intron-variant | CHFR | GRCh38.p7 | 12:132844008 | AACTAGAGCCATGAG[A/G]AAGTCGGGGGCTCCT | 55743 |
rs768155485 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132857854 | TTGAGTTCCCGCGGA[A/G]AAGCAAGGAGGCCCT | 55743 |
rs768249308 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132877099 | CGCGCCCGGGCTGAT[A/G]ATAATGTTTTTTTCA | 55743 |
rs768263118 | snp | G/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132860931 | CTAATTTTTGCATTT[G/T]TAGTAGAGACGGAGT | 55743 |
rs768263846 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132859640 | CAGGTGTGAGCTACC[A/G]CGCCCCACCCTCTTC | 55743 |
rs768264977 | snp | A/C | 6.41622e-05 | 0.00566365 | intron-variant | CHFR | GRCh38.p7 | 12:132848633 | GGGGCCTGAAGAGCC[A/C]GTATTACCACAAAAC | 55743 |
rs768284336 | snp | A/C | 0.000942951 | 0.021693 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132887353 | CATCTGCGGAGACCC[A/C]GGAAACGCCCATGGA | 55743 |
rs768330210 | snp | A/G | 1.64741e-05 | 0.00286998 | synonymous-codon | CHFR | GRCh38.p7 | 12:132872307 | CGGTTCATTCTTCCT[A/G]TACACCAAGTAGATG | 55743 |
rs768361418 | snp | G/T | 3.33195e-05 | 0.0040815 | stop-gained | CHFR | GRCh38.p7 | 12:132851691 | CTGGAAGCAGCAGGT[G/T]CACAGGGCGTGGCTT | 55743 |
rs768368136 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132849439 | CCTCAGACCCACATC[C/G]TTTCTTAAACTGAAC | 55743 |
rs768372108 | snp | A/G | 0.000402172 | 0.0141748 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132887168 | CTCTGCCCGGCCCCG[A/G]CCCCCGGCCCCGGCC | 55743 |
rs768391783 | in-del | -/ATCACC | | | intron-variant | CHFR | GRCh38.p7 | 12:132846658 | AGCTGAGGTGGGCAG[-/ATCACC]TGAAGTCAGAAGTTC | 55743 |
rs768414494 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132856292 | CCACGCCTCTCAGGG[A/G]AGGTGCTAATACTAT | 55743 |
rs768497237 | in-del | -/TCCT | | | upstream-variant-2KB, downstream-variant-500B | CHFR, LOC101928530 | GRCh38.p7 | 12:132888891 | ACTTTGTAGAGAATC[-/TCCT]TCCTTTTCCACATCT | 55743 |
rs768516001 | snp | A/G | 1.77562e-05 | 0.00297956 | intron-variant | CHFR | GRCh38.p7 | 12:132848193 | TTACCTGTTTATAAT[A/G]ATGTCGCAGGAAAGC | 55743 |
rs768517593 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132867731 | ATGGAATGTAAGAAC[A/G]CGAGAGCCAAGCACT | 55743 |
rs768629582 | in-del | -/G | 3.49412e-05 | 0.00417964 | intron-variant | CHFR | GRCh38.p7 | 12:132872438 | TACTTAAAATAACTT[-/G]GGAGTTACAAGATTT | 55743 |
rs768643312 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132843498 | TACCCCAGTTGACTA[C/T]TGGATGTCTTTACAA | 55743 |
rs768675401 | snp | C/G | 1.64746e-05 | 0.00287002 | intron-variant | CHFR | GRCh38.p7 | 12:132856650 | AATTGAAAGGACACA[C/G]CGCCATTCACCGGCA | 55743 |
rs768680290 | in-del | -/A | 1.64795e-05 | 0.00287045 | frameshift-variant | CHFR | GRCh38.p7 | 12:132859152 | CCAGCCGCTGCTCTG[-/A]CGTCCTCGTGGACGG | 55743 |
rs768775618 | snp | C/T | 9.41044e-05 | 0.00685881 | missense, intron-variant | CHFR | GRCh38.p7 | 12:132869766 | GAGGGACCCGGGGAT[C/T]GGCCCCTCGCCCTGC | 55743 |
rs768798394 | snp | A/C | 3.41262e-05 | 0.00413061 | missense | CHFR | GRCh38.p7 | 12:132853482 | CCAGGGCCTGTGGGG[A/C]TCCTGGCTCGCCCTC | 55743 |
rs768814594 | snp | C/T | 4.62599e-05 | 0.00480914 | missense | CHFR | GRCh38.p7 | 12:132853563 | ACTGCCGGCACACGA[C/T]GTATGGCTGGCTGCA | 55743 |
rs768876353 | in-del | -/TGCA | | | intron-variant | CHFR | GRCh38.p7 | 12:132876149 | CACTGCACTTCAGCC[-/TGCA]TGCAACACAGTGAAA | 55743 |
rs768884089 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132862029 | CGTAATCCCAGCACG[C/T]TGGGAGGCCGAAGCA | 55743 |
rs768937103 | snp | A/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132873039 | GAGCAGAGACCTGAC[A/T]GCAAATCAGGTGTTG | 55743 |
rs768948847 | snp | A/G | 1.83613e-05 | 0.0030299 | intron-variant | CHFR | GRCh38.p7 | 12:132857570 | GCAAACTGAAAGTGC[A/G]AGAGGAACAGTGTCC | 55743 |
rs768973864 | snp | C/G | 1.67888e-05 | 0.00289726 | intron-variant | CHFR | GRCh38.p7 | 12:132859240 | CATCTACAGGAGAAA[C/G]GGATGTGTTCTGTCG | 55743 |
rs768997337 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132843164 | CCCAGCAGAGACCCA[A/G]CGACAGACGCTGCGG | 55743 |
rs769011614 | snp | G/T | | | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886830 | TATTTGACCCACCGG[G/T]TGCTTTAAGAGTGTG | 55743 |
rs769092725 | snp | C/T | 1.64768e-05 | 0.00287021 | missense, intron-variant | CHFR | GRCh38.p7 | 12:132870744 | GATTCTTGTGTCATG[C/T]CTTGCTTTTCACTTA | 55743 |
rs769094044 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132853979 | GGAGCCACACCAGGC[A/G]CCTGCAAAGCCCCGA | 55743 |
rs769154353 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132882131 | TTCTTACAAAAACAG[A/G]AAGCAGTATAAATGT | 55743 |
rs769166050 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132881380 | ATCTTGTATCCAGAA[C/T]GTATAGAGAACTCTG | 55743 |
rs769207559 | snp | C/T | 1.72889e-05 | 0.0029401 | synonymous-codon | CHFR | GRCh38.p7 | 12:132851619 | GCGCGGGCACTCACA[C/T]TGCTGAGGGGCGACA | 55743 |
rs769231220 | in-del | -/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132846548 | TGCTGGGATTACAGG[-/C]CGTGAGCCACCACAC | 55743 |
rs769326943 | snp | A/G | | | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132841359 | AGGAGGGCGGGCTGC[A/G]GCCCCCGGGGCTCTG | 55743 |
rs769369347 | in-del | -/TG | 2.21442e-05 | 0.0033274 | intron-variant | CHFR | GRCh38.p7 | 12:132877700 | TATGATCGTGGTAAC[-/TG]TGAACACTACTGCAC | 55743 |
rs769371058 | snp | C/T | 4.97228e-05 | 0.00498587 | synonymous-codon | CHFR | GRCh38.p7 | 12:132857499 | GGTAGGACACAGGGA[C/T]GAGCGCTCCATCCAG | 55743 |
rs769390192 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | CHFR, LOC101928530 | GRCh38.p7 | 12:132888478 | TAAAACAAACCATAT[A/G]TACACACATATATAC | 55743 |
rs769505625 | snp | C/T | 1.64825e-05 | 0.00287071 | synonymous-codon | CHFR | GRCh38.p7 | 12:132861576 | GGCAAAGCTGGAGAC[C/T]TCATCACTTGCCACA | 55743 |
rs769506110 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132859596 | ACCTCGTGATCCACC[C/T]GCCTCGGCCTCCCAA | 55743 |
rs769545659 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132875907 | TGGCCGGGCGCGATG[A/G]CTCACGCCTGTAATC | 55743 |
rs769549244 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132865890 | TGTTGCCCAAACTGG[C/T]CTTGAACTCCTGGGC | 55743 |
rs769607729 | snp | C/G | 1.64727e-05 | 0.00286986 | missense | CHFR | GRCh38.p7 | 12:132856543 | TCTTCATCAGAAAAA[C/G]ACCGCCTGACTTTGG | 55743 |
rs769631225 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132858585 | ACAAAAAAATTAGCC[A/G]GGCATGGTGGCACAC | 55743 |
rs769734908 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132874017 | GCCTGAGCACCCCTC[C/T]CCTCCAGCCCACCTC | 55743 |
rs769826363 | in-del | -/AAAG | | | intron-variant | CHFR | GRCh38.p7 | 12:132852319 | TCTATTATTTCCTAT[-/AAAG]AGAGGACAAGCCCAT | 55743 |
rs769878915 | snp | C/T | | | synonymous-codon | CHFR | GRCh38.p7 | 12:132859187 | GGCATTTCTACGCGG[C/T]TGTGCGACCAACAAC | 55743 |
rs769914277 | in-del | -/GACA | 5.41267e-05 | 0.00520196 | intron-variant | CHFR | GRCh38.p7 | 12:132851575 | ACCTGACCCCTGAAG[-/GACA]GATAGGAACCCGCCT | 55743 |
rs769922499 | snp | A/G | 3.90541e-05 | 0.00441877 | missense | CHFR | GRCh38.p7 | 12:132843039 | CTTTCACCTGAGTGC[A/G]GCAGTTACGGCCCCA | 55743 |
rs769933100 | snp | A/G | 9.93641e-05 | 0.00704785 | missense | CHFR | GRCh38.p7 | 12:132853451 | GTCAGGCTGACGGAC[A/G]TGGAGGGTGCATCCC | 55743 |
rs770017155 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132871717 | GTGGAGATTGCGGTG[A/G]GCTGAGATTGCGCCA | 55743 |
rs770017902 | in-del | -/CTCACGTG | | | intron-variant | CHFR | GRCh38.p7 | 12:132857301 | GGTGGAGGGACAGCC[-/CTCACGTG]CCCGGGTGCTGCTGG | 55743 |
rs770024875 | snp | C/G | 9.84397e-05 | 0.007015 | intron-variant | CHFR | GRCh38.p7 | 12:132853403 | GTGACTCACGCGAAG[C/G]CTGAGGCCTGAGGGC | 55743 |
rs770024903 | snp | C/T | 1.64904e-05 | 0.00287139 | missense | CHFR | GRCh38.p7 | 12:132859180 | CGGTTTGGGCATTTC[C/T]ACGCGGTTGTGCGAC | 55743 |
rs770034782 | snp | A/G | 4.95642e-05 | 0.00497792 | missense | CHFR | GRCh38.p7 | 12:132857480 | GCTCCACGGGACAGC[A/G]GCAGGTAGGACACAG | 55743 |
rs770056767 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132865395 | AGACCTGGTCTGTCG[C/G]CCAGGCTGGAGTGCA | 55743 |
rs770058786 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132844563 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGCGCC | 55743 |
rs770087246 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132843341 | AGAGGCAGGAGAATC[A/G]CTTGAACCTGGGAGA | 55743 |
rs770100999 | snp | C/T | 3.48602e-05 | 0.00417479 | intron-variant | CHFR | GRCh38.p7 | 12:132872437 | TCTACTTAAAATAAC[C/T]TGGAGTTACAAGATT | 55743 |
rs770123459 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132856164 | CACCCATGACGAGTC[A/G]AAGCAAAGGGAAGGG | 55743 |
rs770126644 | snp | C/T | 3.29745e-05 | 0.00406031 | intron-variant | CHFR | GRCh38.p7 | 12:132870708 | GCACCCACTTCTTTG[C/T]TACACTCTTACTTAC | 55743 |
rs770185579 | snp | A/G | 1.65658e-05 | 0.00287795 | synonymous-codon | CHFR | GRCh38.p7 | 12:132859100 | CAGGTCCTGGCAGAT[A/G]ATGCATGTCAGCGTC | 55743 |
rs770268372 | snp | A/G | 3.13229e-05 | 0.00395733 | intron-variant | CHFR | GRCh38.p7 | 12:132844163 | AGCCAGTTACCCAGC[A/G]ACACCATCTTCCCAA | 55743 |
rs770351568 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132862015 | CGGTGGCTCACACCC[A/G]TAATCCCAGCACGTT | 55743 |
rs770380694 | snp | A/C/G | 3.30591e-05 | 0.00406554 | missense, synonymous-codon | CHFR | GRCh38.p7 | 12:132857415 | CTTGCCTGGATGCTG[A/C/G]ATGAGGTATGCTTCC | 55743 |
rs770399858 | snp | A/G | 1.65154e-05 | 0.00287358 | missense | CHFR | GRCh38.p7 | 12:132847079 | GCTGGAGAGCCACGA[A/G]GCTCTCGGTCAACAT | 55743 |
rs770446660 | in-del | -/AA | | | intron-variant | CHFR | GRCh38.p7 | 12:132842110 | CGAGACTCCATCTCA[-/AA]AAAAAAAAAAAAAAA | 55743 |
rs770455897 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132852966 | GATAGCACCTGGAGC[C/T]CCTTGCTGGAAAAAG | 55743 |
rs770480077 | in-del | -/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132878473 | GACTCCAACTGGAAA[-/T]AAAAAAAAAAAAAAG | 55743 |
rs770508223 | snp | C/T | 8.40301e-05 | 0.00648136 | intron-variant | CHFR | GRCh38.p7 | 12:132848759 | GTTACACGCACTCAG[C/T]GCTGAGGGCTGTCTC | 55743 |
rs770621972 | snp | C/T | 0.000122587 | 0.00782804 | intron-variant | CHFR | GRCh38.p7 | 12:132853577 | ACGTATGGCTGGCTG[C/T]AAGGAAGCACAGGGC | 55743 |
rs770703042 | snp | C/G | 1.66134e-05 | 0.00288208 | intron-variant | CHFR | GRCh38.p7 | 12:132861455 | TGAGGACACACACAA[C/G]CAGACACTAACCTCC | 55743 |
rs770730321 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132875678 | ACTGACACAGACTTC[C/T]CTTCCGAGAAATCAT | 55743 |
rs770759398 | snp | C/T | | | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132887064 | AGAACACCGAATAAA[C/T]ACCAGTTCTTACATG | 55743 |
rs770763697 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132881176 | GAGAGGCTGAGGTGG[A/G]AGAACATGGGAGGTG | 55743 |
rs770777793 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132858392 | AACAAAAAACCACCC[C/T]GGGCTACATGGCGAA | 55743 |
rs770791324 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | CHFR, LOC101928530 | GRCh38.p7 | 12:132888308 | GAGCCCCCAAGGGCG[A/G]TTTTAAGAGGGTGAA | 55743 |
rs770802724 | snp | A/T | | | intron-variant, missense | CHFR | GRCh38.p7 | 12:132862401 | AGTTTTAGACCAGCC[A/T]GGGCAACACAGCAAG | 55743 |
rs770803986 | in-del | -/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132851399 | CCAAGCCGAGCCCCC[-/G]GGTGGATGGAGATGT | 55743 |
rs770805740 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132853856 | GACGTGTGCTCCCAG[A/G]AGACGACGCCAGAGC | 55743 |
rs770812049 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132859337 | CTAACTGTCGTAACC[A/G]AGAAGGAAATACATG | 55743 |
rs770855105 | snp | G/T | 5.10591e-05 | 0.00505242 | missense | CHFR | GRCh38.p7 | 12:132877636 | ACCAGTTTATTGCTG[G/T]GGAAGGAAAGGTCGC | 55743 |
rs770961851 | snp | A/T | 1.64789e-05 | 0.0028704 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132841545 | AAGCTGCTCAGGGCC[A/T]CTGGATGCTTAGTTT | 55743 |
rs771018747 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132876850 | CCCAGGCTGGAGTGC[A/G]GTGGTGCCATCTCAG | 55743 |
rs771058147 | snp | C/T | 1.75869e-05 | 0.00296532 | intron-variant | CHFR | GRCh38.p7 | 12:132851607 | CTGCGTGCGGTGGCG[C/T]GGGCACTCACACTGC | 55743 |
rs771109077 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132864359 | TGGAGAGGAGCACCA[C/T]CTTACCACTTACAGA | 55743 |
rs771123706 | snp | C/T | 3.39864e-05 | 0.00412214 | missense | CHFR | GRCh38.p7 | 12:132859072 | CACGGTCGCACCTCA[C/T]GCAGTCGTGCAGCAG | 55743 |
rs771139880 | in-del | -/AAA | | | intron-variant | CHFR | GRCh38.p7 | 12:132881869 | CAAGACGCTGTCTCA[-/AAA]AAAAAAAAAAAAAAA | 55743 |
rs771143796 | snp | C/T | 1.6476e-05 | 0.00287014 | synonymous-codon | CHFR | GRCh38.p7 | 12:132872292 | TCTCTTACTGTGTTC[C/T]GGTTCATTCTTCCTG | 55743 |
rs771207980 | snp | C/G | 1.65529e-05 | 0.00287683 | intron-variant | CHFR | GRCh38.p7 | 12:132848166 | GAGCTCTGCCGAGAT[C/G]AAGGGGCAATGTTAC | 55743 |
rs771215712 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132855347 | GAATCGCTTGAACCC[A/G]GGAGGCGGAGGTTGC | 55743 |
rs771231844 | snp | C/T | 1.6534e-05 | 0.00287519 | intron-variant | CHFR | GRCh38.p7 | 12:132872242 | GCGCCCTCACGTGCA[C/T]CCCCGTGCGGGTCTG | 55743 |
rs771259995 | snp | A/G | 1.97908e-05 | 0.00314563 | intron-variant | CHFR | GRCh38.p7 | 12:132844146 | TAATCTGGAAGAAAC[A/G]CAGCCAGTTACCCAG | 55743 |
rs771325511 | snp | C/T | 0.000100954 | 0.007104 | intron-variant | CHFR | GRCh38.p7 | 12:132869603 | AGCACCAAGACCTCA[C/T]GAGATGTGACCTCAC | 55743 |
rs771342279 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132865830 | ACACCCGGCTAATTT[C/T]TGTATTTTTTATATT | 55743 |
rs771345344 | in-del | -/ACC | | | intron-variant | CHFR | GRCh38.p7 | 12:132850334 | CTTATAACGCCTACG[-/ACC]ACTTCACCAATGCCT | 55743 |
rs771346118 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132854387 | CACACTCTGTGACTC[A/G]ACTGCTTCACGTCTA | 55743 |
rs771383169 | in-del | -/GC | | | intron-variant | CHFR | GRCh38.p7 | 12:132873148 | GGCCTCAGCTCTGCA[-/GC]TTCACTCCCGAGGCC | 55743 |
rs771383944 | snp | A/G | 1.68952e-05 | 0.00290642 | intron-variant | CHFR | GRCh38.p7 | 12:132851779 | GCACGTGGGACCCAG[A/G]GCAGAAAGACAGCAG | 55743 |
rs771434751 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132857643 | GCAGCAGCCCCACCA[C/T]GGAAGGGCCTACAGG | 55743 |
rs771481759 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132871629 | ATACAAAAATGAGCC[A/G]GGCGTGGTGGTGGGC | 55743 |
rs771500835 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132861911 | TAGCCCTCGAGCACC[A/G]AGTCTAACGCAGGGC | 55743 |
rs771651552 | in-del | -/AAAC | | | intron-variant | CHFR | GRCh38.p7 | 12:132870358 | TCCATCTCAAAAAAC[-/AAAC]AAACAAACAAACAAA | 55743 |
rs771711633 | snp | G/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132880351 | TAATAATAATAAGCT[G/T]AGGTTTGTCAAAAGT | 55743 |
rs771714333 | snp | A/C | 0.00162206 | 0.0284323 | intron-variant, missense | CHFR | GRCh38.p7 | 12:132862413 | GCCTGGGCAACACAG[A/C]AAGGCACCATCTCTA | 55743 |
rs771765496 | snp | G/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132853962 | CGGTGGGCAACGTAC[G/T]GGGAGCCACACCAGG | 55743 |
rs771788815 | snp | A/G | 7.77333e-05 | 0.00623383 | intron-variant | CHFR | GRCh38.p7 | 12:132848751 | GGACACTCGTTACAC[A/G]CACTCAGCGCTGAGG | 55743 |
rs771836352 | in-del | -/GGAGCTCGCGTGC | 1.6507e-05 | 0.00287284 | intron-variant | CHFR | GRCh38.p7 | 12:132856701 | CAGCTCACACTGCTG[-/GGAGCTCGCGTGC]GGAGCTCGCGTGCGC | 55743 |
rs771849929 | snp | C/T | 1.67677e-05 | 0.00289544 | synonymous-codon | CHFR | GRCh38.p7 | 12:132877623 | GTGATCTCCAGAGAC[C/T]AGTTTATTGCTGGGG | 55743 |
rs771852344 | snp | C/T | | | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886930 | AGTCAGAAAAGATAC[C/T]CTGTACGGCAACGAA | 55743 |
rs771858129 | snp | A/C | 1.84728e-05 | 0.00303909 | intron-variant | CHFR | GRCh38.p7 | 12:132877519 | GCTTCTTAAGCTACA[A/C]GAAGAAACACCAAAA | 55743 |
rs771875309 | snp | A/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132867798 | GCCGTGAGACTTCAC[A/T]GAAGAACAGGAAGAG | 55743 |
rs772040473 | snp | C/T | 9.92605e-05 | 0.00704418 | intron-variant | CHFR | GRCh38.p7 | 12:132872236 | CAGAGAGCGCCCTCA[C/T]GTGCACCCCCGTGCG | 55743 |
rs772089817 | snp | A/G | 5.12597e-05 | 0.00506233 | synonymous-codon | CHFR | GRCh38.p7 | 12:132848672 | GCAGCCGTAGCAGCC[A/G]GTCCGGGTGCAGCCC | 55743 |
rs772109721 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132880561 | TACTCAGGAGGCTGA[A/G]GCAGAAGAATGGCGT | 55743 |
rs772208422 | snp | C/T | 1.64787e-05 | 0.00287038 | missense, intron-variant | CHFR | GRCh38.p7 | 12:132870768 | TCACTTAAAGATTCA[C/T]AGAGGTATGCCACGT | 55743 |
rs772249892 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132874151 | CCATCAGACCCATAT[C/T]GGACTCTGGACCTCC | 55743 |
rs772321674 | snp | C/G | 1.64727e-05 | 0.00286986 | missense | CHFR | GRCh38.p7 | 12:132856525 | AGGTCCTCTGAACTC[C/G]CTTCTTCATCAGAAA | 55743 |
rs772346912 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132854165 | GGCCAACAGGTAAGA[C/T]CCAACCAGGTAAAAA | 55743 |
rs772354359 | snp | A/G | 3.98565e-05 | 0.00446393 | synonymous-codon | CHFR | GRCh38.p7 | 12:132843079 | AGGACGGGATGTTAC[A/G]GCCACTGGAAAAAGA | 55743 |
rs772460210 | snp | A/G | 1.66418e-05 | 0.00288455 | missense | CHFR | GRCh38.p7 | 12:132851702 | AGGTGCACAGGGCGT[A/G]GCTTCCTTGCAGAGG | 55743 |
rs772485314 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132875578 | CAGTGAGCCGAGATC[A/G]CACCAACAGCACTTC | 55743 |
rs772496941 | snp | A/G | | | synonymous-codon | CHFR | GRCh38.p7 | 12:132841584 | TGTCTGTTCACAGAT[A/G]TGATTGAATTTCCTG | 55743 |
rs772507556 | snp | A/G | 0.00022531 | 0.0106115 | intron-variant | CHFR | GRCh38.p7 | 12:132857580 | AGTGCAAGAGGAACA[A/G]TGTCCAGACAGTCCC | 55743 |
rs772578551 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132882313 | CCCTGTGTCACGACA[C/T]GCTGGAAGCAGCAGA | 55743 |
rs772594296 | snp | C/T | 1.65078e-05 | 0.00287291 | intron-variant | CHFR | GRCh38.p7 | 12:132870687 | GAATGCTATAGCTCC[C/T]AACATGCACCCACTT | 55743 |
rs772616630 | in-del | -/AC | | | intron-variant | CHFR | GRCh38.p7 | 12:132864849 | CCCTTTTTAAGTAGA[-/AC]ATTATCAAAAAATTA | 55743 |
rs772618862 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132842510 | CTCCTTGGGCCACAG[A/G]AGTGATTTACGTGAT | 55743 |
rs772621871 | in-del | -/CCCGGCCCCGGCC | 6.51105e-05 | 0.00570535 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132887157 | AACCCGGTGGCTCTG[-/CCCGGCCCCGGCC]CCCGGCCCCGGCCCC | 55743 |
rs772716713 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132879536 | GCTGGGATTACAGGC[A/G]CACACCACCAGGGCC | 55743 |
rs772758623 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132880361 | AAGCTGAGGTTTGTC[A/G]AAAGTAAAATGTGGG | 55743 |
rs772840510 | snp | C/T | | | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886114 | TTCAGTTGTTCAAGA[C/T]CAGCCTGGGCAATAT | 55743 |
rs772849776 | snp | C/G/T | 6.78761e-05 | 0.00582531 | intron-variant | CHFR | GRCh38.p7 | 12:132848219 | AAAGCACTGTCTGCC[C/G/T]GACACTGAGGATAAA | 55743 |
rs772931516 | in-del | -/CCT | 1.65329e-05 | 0.0028751 | splice-donor-variant | CHFR | GRCh38.p7 | 12:132861466 | ACAACCAGACACTAA[-/CCT]CCTCTCATTTTCTTC | 55743 |
rs772942836 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132867141 | CTCAAGAACATCAAC[A/G]AACAGGAGAGGTGTG | 55743 |
rs772945632 | snp | C/T | 1.64776e-05 | 0.00287028 | intron-variant | CHFR | GRCh38.p7 | 12:132856656 | AAGGACACAGCGCCA[C/T]TCACCGGCAGTGAGA | 55743 |
rs772976116 | snp | A/G | 6.92913e-05 | 0.00588565 | intron-variant | CHFR | GRCh38.p7 | 12:132857610 | CACAGATGCAACCGC[A/G]ACCCTCGACCAAGGT | 55743 |
rs773033475 | in-del | -/ATATATATATATAT | | | intron-variant | CHFR | GRCh38.p7 | 12:132850967 | TGTATGTGTGTGCAT[-/ATATATATATATAT]ATATATATATATATA | 55743 |
rs773080457 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132860107 | ACCCTCCGTCTCAGC[C/T]GCTCCTCACCCAATT | 55743 |
rs773102049 | snp | C/T | 3.29924e-05 | 0.00406142 | synonymous-codon | CHFR | GRCh38.p7 | 12:132859184 | TTGGGCATTTCTACG[C/T]GGTTGTGCGACCAAC | 55743 |
rs773146658 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132856343 | CAAGCCATTTAAGAG[C/T]TTGGCTGCTCAGGGC | 55743 |
rs773164146 | snp | A/T | 1.64732e-05 | 0.0028699 | missense | CHFR | GRCh38.p7 | 12:132872335 | ATGACATCCCCAGTC[A/T]GTAAAGGGCATGTCT | 55743 |
rs773175700 | snp | A/T | | | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886953 | GCAACGAACGTGACA[A/T]TATTGCATTCTGGAG | 55743 |
rs773496315 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132874370 | AGGACCAGCATTCAG[C/T]GCAAGGAAGCCAGGC | 55743 |
rs773507011 | snp | A/G | 3.37302e-05 | 0.00410658 | intron-variant | CHFR | GRCh38.p7 | 12:132851772 | AGCCGGAGCACGTGG[A/G]ACCCAGGGCAGAAAG | 55743 |
rs773555344 | snp | C/G | 1.64811e-05 | 0.00287059 | missense, intron-variant | CHFR | GRCh38.p7 | 12:132870772 | TTAAAGATTCATAGA[C/G]GTATGCCACGTCTAA | 55743 |
rs773562554 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132869988 | TCGAGGCAGGTGTAT[A/C]TCCTGAGGTCAGGAG | 55743 |
rs773596387 | snp | G/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132864319 | ACTCACGCCATCATC[G/T]CCAGCGCCCCGTGCT | 55743 |
rs773617183 | snp | A/T | 1.69729e-05 | 0.0029131 | missense | CHFR | GRCh38.p7 | 12:132851644 | GCGACACGCGGGTCC[A/T]GCTCGCGCTCCGCTC | 55743 |
rs773617187 | snp | C/T | | | synonymous-codon, intron-variant | CHFR | GRCh38.p7 | 12:132870731 | TTACTTACCAAAGGA[C/T]TCTTGTGTCATGCCT | 55743 |
rs773622366 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132881694 | AACATGGTGAAACCC[C/G]GTCTCTACTAAAGAT | 55743 |
rs773650672 | snp | C/T | 0.000157741 | 0.00887951 | intron-variant | CHFR | GRCh38.p7 | 12:132857607 | TCCCACAGATGCAAC[C/T]GCGACCCTCGACCAA | 55743 |
rs773673137 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132854195 | AACAAGGCACAGTGA[A/C]AAGACATTTTTTTCA | 55743 |
rs773703522 | snp | A/G | 1.66402e-05 | 0.00288441 | synonymous-codon | CHFR | GRCh38.p7 | 12:132851703 | GGTGCACAGGGCGTG[A/G]CTTCCTTGCAGAGGG | 55743 |
rs773747877 | snp | A/T | | | upstream-variant-2KB, downstream-variant-500B | CHFR, LOC101928530 | GRCh38.p7 | 12:132888601 | GAACTGAGTCTCTCA[A/T]CGCCAAAGTTAATCT | 55743 |
rs773758153 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132851924 | GTCAAAACAGATTAA[C/T]AATAACCAAAAATGA | 55743 |
rs773901786 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132860958 | GAGTTTCACCATGTT[A/G]GCCAGGCTGGTCTTG | 55743 |
rs773913714 | in-del | -/AAGTGTCACT | | | intron-variant | CHFR | GRCh38.p7 | 12:132876700 | GGGTCATAGACACCA[-/AAGTGTCACT]AAGTGTCCCATCCTG | 55743 |
rs774002945 | snp | A/G | 1.92077e-05 | 0.00309895 | synonymous-codon | CHFR | GRCh38.p7 | 12:132843064 | GCCCCAGTAGCAGTC[A/G]GGACGGGATGTTACG | 55743 |
rs774033823 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132877194 | GTGTTTAGATAAATA[A/C]TCTTACCATTGTGTT | 55743 |
rs774050380 | snp | G/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132883709 | TCCAGACTGGATAAA[G/T]AGCTCTTTGGGAAAA | 55743 |
rs774070010 | snp | A/C | 1.65141e-05 | 0.00287346 | missense | CHFR | GRCh38.p7 | 12:132861601 | GCCACAGAGGGACCA[A/C]TTCCTTTAGGGGAGA | 55743 |
rs774077780 | snp | G/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132867026 | GCAACAGAGCAAGAC[G/T]CTGTCTCAAAAAAAC | 55743 |
rs774088247 | snp | A/G | 2.00487e-05 | 0.00316606 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132887366 | CCCGGAAACGCCCAT[A/G]GAGACTCCCGACCCC | 55743 |
rs774088595 | snp | A/C | 1.64751e-05 | 0.00287007 | missense | CHFR | GRCh38.p7 | 12:132861501 | CACGGGCTCCAAATC[A/C]TCCTGATCCTGGGGT | 55743 |
rs774111922 | snp | C/T | 1.81266e-05 | 0.00301048 | intron-variant | CHFR | GRCh38.p7 | 12:132848198 | TGTTTATAATGATGT[C/T]GCAGGAAAGCACTGT | 55743 |
rs774176417 | snp | A/G | 3.1272e-05 | 0.00395411 | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132887180 | CCGGCCCCCGGCCCC[A/G]GCCTCAGCCCCGCAC | 55743 |
rs774239471 | snp | C/T | 1.64738e-05 | 0.00286995 | missense | CHFR | GRCh38.p7 | 12:132872312 | CATTCTTCCTGTACA[C/T]CAAGTAGATGACATC | 55743 |
rs774459483 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132862039 | GCACGTTGGGAGGCC[A/G]AAGCAAGTGGATCAC | 55743 |
rs774506010 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132873051 | GACAGCAAATCAGGT[A/G]TTGGTCAGGTGACCA | 55743 |
rs774523092 | in-del | -/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132879005 | TTTTTTTTTGTTTTT[-/G]TTTGTTTTTTTTTTT | 55743 |
rs774539804 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132843557 | ATGAGTAACTGCAAA[C/T]AGACCCAGGGCCTAA | 55743 |
rs774580014 | snp | A/G | 1.68108e-05 | 0.00289916 | intron-variant | CHFR | GRCh38.p7 | 12:132859242 | TCTACAGGAGAAAGG[A/G]ATGTGTTCTGTCGTA | 55743 |
rs774658371 | snp | C/T | 1.73444e-05 | 0.00294481 | missense | CHFR | GRCh38.p7 | 12:132853491 | GTGGGGCTCCTGGCT[C/T]GCCCTCGGGTGCTGG | 55743 |
rs774699430 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132881416 | TCAATAAATAGAAAG[C/T]AAATAATGCAACTTA | 55743 |
rs774738670 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132873945 | TGCCGCTCACCACAC[A/G]CTCCGACCACACAGC | 55743 |
rs774755493 | in-del | -/A | | | intron-variant | CHFR | GRCh38.p7 | 12:132880844 | GTGGCGGGCGCCTAT[-/A]ATCCCAGCTACACGG | 55743 |
rs774768503 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132853095 | TGAGGGACAGATATG[C/T]GATCATCACTTTGGG | 55743 |
rs774770261 | snp | A/C | 3.3295e-05 | 0.00408 | missense | CHFR | GRCh38.p7 | 12:132857515 | GAGCGCTCCATCCAG[A/C]CCGAGTAGCAAGCCG | 55743 |
rs774819581 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132863384 | TGGTGGCACATGCCT[A/G]TAACCCAGCTACTTG | 55743 |
rs774858017 | snp | C/T | 3.30082e-05 | 0.00406239 | missense | CHFR | GRCh38.p7 | 12:132857440 | GCTTCCACGAGGTTG[C/T]TGAGGATGTGGTTTT | 55743 |
rs775072924 | snp | A/G | 1.64944e-05 | 0.00287175 | intron-variant | CHFR | GRCh38.p7 | 12:132841625 | ATGGCCAAATTACAC[A/G]AGAGAGCATTGGAGA | 55743 |
rs775108018 | snp | G/T | 1.64746e-05 | 0.00287002 | intron-variant | CHFR | GRCh38.p7 | 12:132859267 | GTCGTAACCAAGAAG[G/T]AAATACACGCAGGTT | 55743 |
rs775167699 | in-del | -/CCGCCCTCACGTGCCCGGGTGCTGGTGTGGATG | 1.69867e-05 | 0.00291429 | intron-variant | CHFR | GRCh38.p7 | 12:132857361 | GTGGTGGTGGAGGGA[lengthTooLong]CCCTCACTTGCCTGG | 55743 |
rs775195359 | in-del | -/CT | | | intron-variant | CHFR | GRCh38.p7 | 12:132846263 | TTCATGCTTAACTGT[-/CT]TTTTTTTTTTTTTTT | 55743 |
rs775199616 | snp | A/G | 7.03037e-05 | 0.00592848 | synonymous-codon | CHFR | GRCh38.p7 | 12:132877650 | GGGGAAGGAAAGGTC[A/G]CAACCTAAAAAAGAG | 55743 |
rs775202274 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132848236 | ACACTGAGGATAAAC[A/G]TATTTCTTTTCATTA | 55743 |
rs775208965 | snp | C/T | | | missense, intron-variant | CHFR | GRCh38.p7 | 12:132869730 | GTTCCTCAAAGCACA[C/T]CTGAGTGGCGGGCGA | 55743 |
rs775232160 | snp | A/G | 1.66244e-05 | 0.00288304 | intron-variant | CHFR | GRCh38.p7 | 12:132848172 | TGCCGAGATGAAGGG[A/G]CAATGTTACCTGTTT | 55743 |
rs775237770 | in-del | -/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132867927 | AAAGCTAATTCAAAA[-/C]ATAATCTAGAATAGA | 55743 |
rs775242919 | snp | A/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132847503 | TGTTCTCTGTGCCCT[A/T]CAAACACACACGAGC | 55743 |
rs775309126 | snp | C/T | 1.64803e-05 | 0.00287052 | missense | CHFR | GRCh38.p7 | 12:132861488 | TCATTTTCTTCTTCA[C/T]GGGCTCCAAATCCTC | 55743 |
rs775313907 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132859620 | CTCCCAAAGTACTAG[A/G]GTAACAGGTGTGAGC | 55743 |
rs775330479 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132875910 | CCGGGCGCGATGGCT[C/T]ACGCCTGTAATCCCA | 55743 |
rs775371729 | snp | C/G | | | upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132887804 | GAAGTGGCTGCGGTC[C/G]GCGCCATGTTATGTT | 55743 |
rs775426850 | snp | C/T | 0.000287522 | 0.0119866 | intron-variant | CHFR | GRCh38.p7 | 12:132853608 | CGAGCTGTGTGCAGG[C/T]CCCAAGCCTCTCAGG | 55743 |
rs775693436 | snp | C/T | 3.61213e-05 | 0.00424963 | intron-variant | CHFR | GRCh38.p7 | 12:132851567 | GCTTTGAAACCTGAC[C/T]CCTGAAGGACAGATA | 55743 |
rs775693581 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132869590 | AAACCATGCAACCAG[C/T]ACCAAGACCTCATGA | 55743 |
rs775702171 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132842774 | GATGGGGTGTGCCCC[A/G]GATGCCTCAGACAAC | 55743 |
rs775767314 | snp | A/G | 5.01467e-05 | 0.00500708 | missense | CHFR | GRCh38.p7 | 12:132853455 | GGCTGACGGACGTGG[A/G]GGGTGCATCCCCCAG | 55743 |
rs775769340 | snp | A/G | 3.31148e-05 | 0.00406894 | missense | CHFR | GRCh38.p7 | 12:132844057 | CAGGAATGTTCTGCC[A/G]ATACTGATAGGTCAG | 55743 |
rs775787800 | snp | A/G | 4.88245e-05 | 0.00494064 | intron-variant | CHFR | GRCh38.p7 | 12:132853407 | CTCACGCGAAGGCTG[A/G]GGCCTGAGGGCGGCG | 55743 |
rs775799321 | snp | C/T | 3.30469e-05 | 0.00406477 | synonymous-codon | CHFR | GRCh38.p7 | 12:132859112 | GATGATGCATGTCAG[C/T]GTCTCCTCCATCTTG | 55743 |
rs775805064 | snp | C/T | 3.31719e-05 | 0.00407245 | missense | CHFR | GRCh38.p7 | 12:132857503 | GGACACAGGGACGAG[C/T]GCTCCATCCAGCCCG | 55743 |
rs775805219 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132885769 | AGTAGGTACATAGGC[A/G]CAGAAAGATGTCGTT | 55743 |
rs775817107 | snp | A/G/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132862028 | CCGTAATCCCAGCAC[A/G/T]TTGGGAGGCCGAAGC | 55743 |
rs775863635 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132843394 | TCACACCACTGCACT[C/T]CAGCCTGGGCGACAG | 55743 |
rs775872286 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132861406 | ACGGAGCATGGCAGC[A/G]GCCCCCGCATGCCCC | 55743 |
rs775898959 | snp | C/T | 1.65075e-05 | 0.00287289 | missense | CHFR | GRCh38.p7 | 12:132857432 | TGAGGTATGCTTCCA[C/T]GAGGTTGTTGAGGAT | 55743 |
rs775962862 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132872891 | CATGGCCCTGCACTC[A/C]GAGCTTGTGGTCTGG | 55743 |
rs775978433 | snp | A/C | 0.000100103 | 0.00707402 | missense | CHFR | GRCh38.p7 | 12:132851676 | CCGGTCGGGCATGGG[A/C]TGGAAGCAGCAGGTG | 55743 |
rs776005190 | snp | C/T | 0.000100477 | 0.00708721 | missense, intron-variant | CHFR | GRCh38.p7 | 12:132869639 | CTGGAGGAACGCTCT[C/T]GCCCTGCAGGAGAAG | 55743 |
rs776170766 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132853012 | ACATTTCGCATTAAG[C/G]CAACTCTGGTGACGC | 55743 |
rs776171609 | snp | C/G | 1.70072e-05 | 0.00291605 | intron-variant | CHFR | GRCh38.p7 | 12:132857352 | CGTGCCTGGGTGGTG[C/G]TGGAGGGACCGCCCT | 55743 |
rs776204190 | snp | A/T | | | downstream-variant-500B | CHFR | GRCh38.p7 | 12:132840159 | AGCCTCCACACTGGA[A/T]GAACAGGTTGTGGCT | 55743 |
rs776221948 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132867896 | AATCTCAAAAAGATT[C/T]TTCTATTAAACTGGA | 55743 |
rs776255075 | snp | A/G | 1.7528e-05 | 0.00296036 | intron-variant | CHFR | GRCh38.p7 | 12:132877543 | ACCAAAAGAAGCTCA[A/G]AACATACTCACCTGG | 55743 |
rs776280817 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132847286 | GGGCTGCACGTTCAC[A/G]GCCTGCAGCACGAGA | 55743 |
rs776346024 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | CHFR, LOC101928530 | GRCh38.p7 | 12:132888392 | AGGCAGGAGGATCTC[A/G]AGCCCAGGAGTTCGA | 55743 |
rs776373151 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132857702 | CTTTAAGTCAGTCTT[A/G]GTTAATGAAAAGAAA | 55743 |
rs776390811 | snp | A/T | 3.29451e-05 | 0.00405851 | missense | CHFR | GRCh38.p7 | 12:132856539 | CCCTTCTTCATCAGA[A/T]AAAGACCGCCTGACT | 55743 |
rs776454052 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132869384 | ACTTTTATGGTATGC[A/G]AATTATAGTCTCAAT | 55743 |
rs776466473 | snp | C/T | 1.65504e-05 | 0.00287662 | missense | CHFR | GRCh38.p7 | 12:132847118 | ATGTCAAACCTCTGG[C/T]TGCCAGGTAATTCTG | 55743 |
rs776467669 | snp | A/G/T | 5.14084e-05 | 0.00506972 | missense | CHFR | GRCh38.p7 | 12:132877640 | GTTTATTGCTGGGGA[A/G/T]GGAAAGGTCGCAACC | 55743 |
rs776471313 | snp | G/T | | | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132887085 | TTCTTACATGACATT[G/T]CACTCCACGGAAAAA | 55743 |
rs776480867 | in-del | -/AA | | | intron-variant | CHFR | GRCh38.p7 | 12:132881870 | AAGACGCTGTCTCAA[-/AA]AAAAAAAAAAAAAAA | 55743 |
rs776559124 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132865864 | TTTTTTGTAAAGATA[C/T]GGTTTCACCATGTTG | 55743 |
rs776642806 | snp | C/T | 1.66568e-05 | 0.00288585 | missense | CHFR | GRCh38.p7 | 12:132851723 | CTTGCAGAGGGCACA[C/T]GTAATCCTGGACTGC | 55743 |
rs776670620 | snp | C/T | 1.64789e-05 | 0.0028704 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132841546 | AGCTGCTCAGGGCCT[C/T]TGGATGCTTAGTTTT | 55743 |
rs776704688 | in-del | -/AG | 0.000218035 | 0.0104389 | intron-variant | CHFR | GRCh38.p7 | 12:132877662 | GTCGCAACCTAAAAA[-/AG]AGAGGGTGGGTCAAC | 55743 |
rs776748296 | snp | A/G | 4.95282e-05 | 0.00497611 | intron-variant | CHFR | GRCh38.p7 | 12:132853380 | TCAGCACCGGGCACA[A/G]CCACAAAGTGACTCA | 55743 |
rs776753889 | in-del | -/A | 1.65419e-05 | 0.00287588 | frameshift-variant | CHFR | GRCh38.p7 | 12:132859203 | GTGCGACCAACAACT[-/A]GCCCGTTCAGGTCAA | 55743 |
rs776799231 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132842478 | TGAGGGCACTGTCTC[C/G]ATCACTTTAATCTGA | 55743 |
rs776809342 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132864627 | CCGAGTAGCTGGGAT[C/T]ACAGGCGCCCGCAAC | 55743 |
rs776872240 | snp | C/G | 2.17252e-05 | 0.00329577 | intron-variant | CHFR | GRCh38.p7 | 12:132844153 | GAAGAAACACAGCCA[C/G]TTACCCAGCAACACC | 55743 |
rs776904899 | snp | C/G | 0.000100974 | 0.00710472 | intron-variant | CHFR | GRCh38.p7 | 12:132869604 | GCACCAAGACCTCAT[C/G]AGATGTGACCTCACC | 55743 |
rs776915637 | snp | A/G | 3.39023e-05 | 0.00411704 | synonymous-codon | CHFR | GRCh38.p7 | 12:132859073 | ACGGTCGCACCTCAC[A/G]CAGTCGTGCAGCAGG | 55743 |
rs776920849 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132871633 | AAAAATGAGCCGGGC[A/G]TGGTGGTGGGCACCT | 55743 |
rs776937997 | snp | A/G | 2.24914e-05 | 0.00335338 | intron-variant | CHFR | GRCh38.p7 | 12:132857608 | CCCACAGATGCAACC[A/G]CGACCCTCGACCAAG | 55743 |
rs776942224 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132842667 | GCCTGCTCACGGGAC[A/G]GACGAGAACCCAGCT | 55743 |
rs776981925 | in-del | -/AT | | | intron-variant | CHFR | GRCh38.p7 | 12:132845650 | GCAAGAACCTGTCTC[-/AT]ATATATATTTCTACA | 55743 |
rs776983762 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132855540 | GGTGTGGTGGCATGC[A/G]CCTGTAGTCCCAGCT | 55743 |
rs776993899 | snp | G/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132860215 | ATGGTACATTTGATT[G/T]ATCAATTTTAGACAT | 55743 |
rs777028366 | snp | C/G/T | 6.61108e-05 | 0.00574907 | intron-variant | CHFR | GRCh38.p7 | 12:132872246 | CCTCACGTGCACCCC[C/G/T]GTGCGGGTCTGACCC | 55743 |
rs777043526 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132870951 | AGTAATCTAAAACAT[C/T]TCTACCAACACAAAA | 55743 |
rs777073610 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132876168 | AACACAGTGAAACTC[A/C]ATCTCAAAAAAAAAA | 55743 |
rs777150024 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132861163 | TTAGGATTACGGATA[C/T]GAACTACTGCACCTG | 55743 |
rs777155485 | snp | C/G | 1.65985e-05 | 0.00288079 | missense | CHFR | GRCh38.p7 | 12:132844036 | CCTTACCTGGCAACT[C/G]GGAAGCAGGAATGTT | 55743 |
rs777186106 | snp | A/C | 5.02508e-05 | 0.00501227 | missense | CHFR | GRCh38.p7 | 12:132861625 | GGGGAGATGCCACCA[A/C]CCCCAGACCCTGTGA | 55743 |
rs777219646 | snp | C/G | 0.000304553 | 0.0123363 | synonymous-codon, intron-variant | CHFR | GRCh38.p7 | 12:132869743 | CACCTGAGTGGCGGG[C/G]GACGACGGAGGGACC | 55743 |
rs777240371 | snp | C/T | 5.6722e-05 | 0.0053252 | synonymous-codon | CHFR | GRCh38.p7 | 12:132853525 | GTGGGGAGGCTGCGC[C/T]GCCTGCCTTCTGTAC | 55743 |
rs777268583 | snp | A/G | 1.65334e-05 | 0.00287514 | intron-variant | CHFR | GRCh38.p7 | 12:132847023 | TGCGCCTTAGAGCAG[A/G]AGGCAACAGAAGAAC | 55743 |
rs777309303 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132861936 | CAGGGCAAACCCACA[C/T]ACCCGTGGTCATATG | 55743 |
rs777311364 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132873467 | AGATGCACTTATACA[C/T]GGGTTTTTTTCAATG | 55743 |
rs777319138 | snp | A/G | 0.000459929 | 0.0151576 | intron-variant | CHFR | GRCh38.p7 | 12:132869878 | CACAACCAGGGCTCA[A/G]GCAGACACTCTAGGG | 55743 |
rs777384785 | in-del | -/A | | | intron-variant | CHFR | GRCh38.p7 | 12:132884232 | AAGACCAGCCTGACG[-/A]ACATGGAGAAACCCC | 55743 |
rs777416500 | snp | C/G | 1.64795e-05 | 0.00287045 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132841538 | GTGCTGAAAGCTGCT[C/G]AGGGCCTCTGGATGC | 55743 |
rs777568602 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132872216 | ATGTAGCCAGGAGGA[A/G]CGTTCAGAGAGCGCC | 55743 |
rs777595033 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132853373 | GTGCACGTCAGCACC[A/G]GGCACAGCCACAAAG | 55743 |
rs777597930 | snp | A/G | | | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132841276 | CCCTCTCGGCGGGAC[A/G]GCCGCATGTTACAGA | 55743 |
rs777709924 | snp | A/G | 1.69694e-05 | 0.0029128 | intron-variant | CHFR | GRCh38.p7 | 12:132848267 | CAGATTCTAGAAAGA[A/G]TAAGAAGTTCAATGA | 55743 |
rs777725012 | snp | G/T | 1.7673e-05 | 0.00297257 | intron-variant | CHFR | GRCh38.p7 | 12:132851603 | CCGCCTGCGTGCGGT[G/T]GCGCGGGCACTCACA | 55743 |
rs777769771 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132858243 | CGCATGCCTGTAGTC[C/T]CAGCTACTTGGGAGG | 55743 |
rs777795345 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132847863 | TGGTGGCAGGAGGCA[C/G]AAAAACGAAATACCT | 55743 |
rs777838067 | in-del | -/TCT | 1.64863e-05 | 0.00287104 | intron-variant | CHFR | GRCh38.p7 | 12:132872275 | CCCGGCAAGCCTTCC[-/TCT]CTCTTACTGTGTTCC | 55743 |
rs777842243 | snp | A/C/T | 6.60997e-05 | 0.00574857 | intron-variant | CHFR | GRCh38.p7 | 12:132856710 | ACTGCTGGGAGCTCG[A/C/T]GTGCGCAGTGCTGCG | 55743 |
rs777921940 | snp | C/T | 1.65089e-05 | 0.00287301 | synonymous-codon | CHFR | GRCh38.p7 | 12:132848154 | GTCACCCAGGTTGAG[C/T]TCTGCCGAGATGAAG | 55743 |
rs777930523 | snp | C/T | 1.6473e-05 | 0.00286988 | missense | CHFR | GRCh38.p7 | 12:132856603 | CTGGCATCCATACTT[C/T]GCACATCTTCTTCAC | 55743 |
rs777937873 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132875619 | ACAGAGCGAGACTCC[A/G]TCTCAAAAAAGAGAA | 55743 |
rs777961507 | in-del | -/TT | 1.64735e-05 | 0.00286993 | frameshift-variant | CHFR | GRCh38.p7 | 12:132856627 | TCTTCACTGCGACTC[-/TT]GTCTAGAATTGAAAG | 55743 |
rs777994408 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132854989 | GCTCACACCTATAAT[C/T]CCAGCACTTTGAGAG | 55743 |
rs778046021 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132878179 | ACAGCCTCTTAAATG[A/G]CAATTTTACAGCCAG | 55743 |
rs778049215 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132846193 | GCAGTAGTGGCAGTC[A/G]GCCACACCCACCCTC | 55743 |
rs778078807 | snp | C/T | 5.2149e-05 | 0.00510605 | intron-variant | CHFR | GRCh38.p7 | 12:132859063 | AAGGGTGAACACGGT[C/T]GCACCTCACGCAGTC | 55743 |
rs778154444 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132842545 | TAACCTAAGAGATGC[C/G]TCCTGACCTACGCCT | 55743 |
rs778169456 | snp | A/C | 4.72066e-05 | 0.00485809 | missense | CHFR | GRCh38.p7 | 12:132853439 | GGCTCACCTGTCGTC[A/C]GGCTGACGGACGTGG | 55743 |
rs778270700 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132872667 | GCTGGGTTCTCTCCC[C/T]GTTTGCCTCCTAGTG | 55743 |
rs778274217 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132866744 | AGGAATGTTACAACA[C/T]ACTGGAATGTTACAA | 55743 |
rs778301903 | snp | A/G | 2.14117e-05 | 0.00327191 | intron-variant | CHFR | GRCh38.p7 | 12:132843098 | ACTGGAAAAAGAGAA[A/G]GGGTACGCATCTATG | 55743 |
rs778303479 | snp | A/G | 1.68403e-05 | 0.0029017 | intron-variant | CHFR | GRCh38.p7 | 12:132844010 | CTAGAGCCATGAGGA[A/G]GTCGGGGGCTCCTTA | 55743 |
rs778361905 | snp | A/C | 3.36564e-05 | 0.00410208 | intron-variant | CHFR | GRCh38.p7 | 12:132872415 | AAAAAACAAAAACAC[A/C]ATTTATTCTACTTAA | 55743 |
rs778392987 | snp | A/T | 1.66955e-05 | 0.0028892 | missense | CHFR | GRCh38.p7 | 12:132844099 | TGCGCAGGCCACAGC[A/T]GTAACACAGAACGGT | 55743 |
rs778406726 | in-del | -/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132872509 | CTGGAAATACTCATA[-/G]GAACAGTGTAAATAC | 55743 |
rs778449705 | snp | C/T | 4.9436e-05 | 0.00497148 | missense | CHFR | GRCh38.p7 | 12:132872287 | TCCTCTCTCTTACTG[C/T]GTTCCGGTTCATTCT | 55743 |
rs778501443 | snp | A/C/G | 8.42828e-05 | 0.00649116 | intron-variant | CHFR | GRCh38.p7 | 12:132851768 | ATTCAGCCGGAGCAC[A/C/G]TGGGACCCAGGGCAG | 55743 |
rs778529060 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132871589 | CCAGCCTGTCCAGCA[C/T]GGCAAAACCCCGTCT | 55743 |
rs778546638 | snp | A/G | 0.000137931 | 0.0083034 | intron-variant | CHFR | GRCh38.p7 | 12:132848744 | GGAGAGAGGACACTC[A/G]TTACACGCACTCAGC | 55743 |
rs778715024 | snp | C/T | | | | | GRCh38.p7 | 12:132880278 | CAAAAATCTTAGTGC[C/T]GTTGGGTCTTGCATG | 55743 |
rs778828908 | snp | A/C | 1.6473e-05 | 0.00286988 | missense | CHFR | GRCh38.p7 | 12:132856593 | GATTTTATTTCTGGC[A/C]TCCATACTTTGCACA | 55743 |
rs778929950 | snp | A/G | 9.48632e-05 | 0.00688641 | missense, intron-variant | CHFR | GRCh38.p7 | 12:132869699 | AAGAGGTCTGACGTC[A/G]ATGTTGATGGCTGTG | 55743 |
rs778961458 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132858056 | TCCTTGTTGGTGCCA[C/T]GAGTAGAATGAAAGT | 55743 |
rs778962027 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132847731 | GCCAGAAGAGACAGG[A/G]ACCAGAGAAAAGGCC | 55743 |
rs778968979 | in-del | -/A | | | intron-variant | CHFR | GRCh38.p7 | 12:132844770 | CGAGTAGCTGGGACT[-/A]CAGGTGTGTGCCACC | 55743 |
rs779016496 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132868307 | CATCCTGGCTAACAC[A/G]GTGAAACTCCGTCTC | 55743 |
rs779021805 | snp | A/C | 1.65143e-05 | 0.00287348 | intron-variant | CHFR | GRCh38.p7 | 12:132848061 | ATGTGGCTCCCGGCT[A/C]CCCAGCCCGCAGCGA | 55743 |
rs779040932 | snp | A/G | 3.34191e-05 | 0.0040876 | intron-variant | CHFR | GRCh38.p7 | 12:132861444 | CACGAGAGGACTGAG[A/G]ACACACACAACCAGA | 55743 |
rs779062860 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132851609 | GCGTGCGGTGGCGCG[A/G]GCACTCACACTGCTG | 55743 |
rs779111370 | snp | A/T | 3.29565e-05 | 0.00405921 | missense | CHFR | GRCh38.p7 | 12:132856483 | CTAATGTCTGAGGAC[A/T]CACTGTCAACGTCTG | 55743 |
rs779135921 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132864106 | CTATATCTTAATAAA[A/G]ACTTAGTTTATCATA | 55743 |
rs779181880 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132849159 | TCACCATGTTGCCCA[C/G]GATGGTTTCAAACTC | 55743 |
rs779200937 | in-del | -/TCTATAC | | | intron-variant | CHFR | GRCh38.p7 | 12:132842069 | AGCTGAGATCACACC[-/TCTATAC]TCCAGCCTGGCAGAC | 55743 |
rs779232926 | in-del | -/TG | | | splice-acceptor-variant | CHFR | GRCh38.p7 | 12:132872396 | CTGTTCCACTGGTGC[-/TG]TAAAAAAACAAAAAC | 55743 |
rs779235326 | snp | A/G | 2.29634e-05 | 0.00338839 | missense | CHFR | GRCh38.p7 | 12:132843011 | CCCAGCTGCACTCAC[A/G]TGGCGTGGTGAGCTT | 55743 |
rs779297834 | snp | C/G | | | upstream-variant-2KB, intron-variant | CHFR, LOC101928530 | GRCh38.p7 | 12:132888094 | CGGGGTCTTCCTGTT[C/G]TGAACGCGCGTAACT | 55743 |
rs779319552 | snp | A/G | 1.85235e-05 | 0.00304326 | intron-variant | CHFR | GRCh38.p7 | 12:132857574 | ACTGAAAGTGCAAGA[A/G]GAACAGTGTCCAGAC | 55743 |
rs779371232 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132882992 | CAGGCATGAGCCACC[A/G]TGCCTGGCCTGAATA | 55743 |
rs779402953 | snp | A/G | 1.64947e-05 | 0.00287177 | intron-variant | CHFR | GRCh38.p7 | 12:132872268 | GTCTGACCCCGGCAA[A/G]CCTTCCTCTCTCTTA | 55743 |
rs779410592 | snp | A/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132876560 | GAGAATTTATTAGTT[A/T]TAAAAAATGATTTTT | 55743 |
rs779420556 | snp | A/C | 1.92081e-05 | 0.00309898 | missense | CHFR | GRCh38.p7 | 12:132843047 | TGAGTGCGGCAGTTA[A/C]GGCCCCAGTAGCAGT | 55743 |
rs779428332 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132854968 | AATTAGCGGCCGGGC[A/G]CGGTGGCTCACACCT | 55743 |
rs779441212 | snp | C/T | 1.66804e-05 | 0.00288789 | missense | CHFR | GRCh38.p7 | 12:132851677 | CGGTCGGGCATGGGC[C/T]GGAAGCAGCAGGTGC | 55743 |
rs779469230 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132881638 | TTTGGGAGGCCGAGG[A/C]GGGCGGATCACATGG | 55743 |
rs779551849 | snp | C/G | 1.84937e-05 | 0.00304081 | intron-variant | CHFR | GRCh38.p7 | 12:132859041 | GCAGTGCCATGTTCC[C/G]TGAGCCAAGGGTGAA | 55743 |
rs779606885 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132871413 | GCTGAGATCACGCCA[C/T]TGCACTCCAGCCTCC | 55743 |
rs779678693 | snp | G/T | 1.65367e-05 | 0.00287543 | intron-variant | CHFR | GRCh38.p7 | 12:132856713 | GCTGGGAGCTCGCGT[G/T]CGCAGTGCTGCGGAA | 55743 |
rs779738580 | snp | G/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132842888 | GGATTTCTAAATGAA[G/T]ATACCGGTTCCTAAA | 55743 |
rs779770632 | snp | A/G | 1.95884e-05 | 0.00312951 | intron-variant | CHFR | GRCh38.p7 | 12:132861681 | ATCCATCCAGCTCAG[A/G]AGAGAACCATGCCTG | 55743 |
rs779847570 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132875491 | AGCTAGGCGTGGCGG[C/G]GGGCACCTGTAATCC | 55743 |
rs779956437 | snp | A/C/G | 8.23654e-05 | 0.00641691 | intron-variant | CHFR | GRCh38.p7 | 12:132856639 | CTCTTGTCTAGAATT[A/C/G]AAAGGACACAGCGCC | 55743 |
rs780047785 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132860866 | CAAGCAATTCTCCTG[C/T]CTCAGCCTTCCAAGT | 55743 |
rs780095590 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132867699 | GCTCTTCTGTTCATA[A/G]GAATCTGCAGACTGC | 55743 |
rs780118329 | snp | A/G | 4.94385e-05 | 0.0049716 | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132841528 | TTCACCTCCAGTGCT[A/G]AAAGCTGCTCAGGGC | 55743 |
rs780149008 | snp | A/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132880077 | AGCTGATTCTAAAGT[A/T]CACAGAAAAAACGTG | 55743 |
rs780154354 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132850785 | GCAGGAGCCAACCGC[A/G]GTGCTCAACAGGGCT | 55743 |
rs780160238 | snp | C/T | 1.86066e-05 | 0.00305007 | intron-variant | CHFR | GRCh38.p7 | 12:132877507 | GCACGAAGTCAGGCT[C/T]CTTAAGCTACAAGAA | 55743 |
rs780237239 | snp | C/T | 1.67494e-05 | 0.00289386 | intron-variant | CHFR | GRCh38.p7 | 12:132859231 | CAAGGTCCCCATCTA[C/T]AGGAGAAAGGGATGT | 55743 |
rs780255609 | snp | G/T | 1.66854e-05 | 0.00288833 | synonymous-codon | CHFR | GRCh38.p7 | 12:132877614 | AATTCTACAGTGATC[G/T]CCAGAGACCAGTTTA | 55743 |
rs780319682 | in-del | -/A | | | intron-variant | CHFR | GRCh38.p7 | 12:132858418 | CGAAACCGTCTCTAC[-/A]AAAAAACACAAAAAT | 55743 |
rs780349155 | snp | C/T | | | intron-variant, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132886765 | ATACCTTTTGGTGTA[C/T]TCTATTTTTGTTTCA | 55743 |
rs780460479 | snp | C/T | 1.6477e-05 | 0.00287024 | missense, intron-variant | CHFR | GRCh38.p7 | 12:132870733 | ACTTACCAAAGGATT[C/T]TTGTGTCATGCCTTG | 55743 |
rs780565079 | snp | G/T | 4.94572e-05 | 0.00497254 | missense | CHFR | GRCh38.p7 | 12:132848114 | ACTCGTAGCTGTTGT[G/T]GTTCAGCACGCCGTC | 55743 |
rs780583670 | snp | A/C | 1.65263e-05 | 0.00287452 | intron-variant | CHFR | GRCh38.p7 | 12:132848056 | AGAAAATGTGGCTCC[A/C]GGCTCCCCAGCCCGC | 55743 |
rs780594986 | snp | G/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132863018 | TCTCCTGCCTCAGCC[G/T]CCTGAGTAGCTGGGA | 55743 |
rs780623191 | snp | A/C | 1.65474e-05 | 0.00287636 | missense | CHFR | GRCh38.p7 | 12:132857490 | ACAGCGGCAGGTAGG[A/C]CACAGGGACGAGCGC | 55743 |
rs780639485 | snp | C/T | 1.65048e-05 | 0.00287265 | intron-variant | CHFR | GRCh38.p7 | 12:132870694 | ATAGCTCCTAACATG[C/T]ACCCACTTCTTTGCT | 55743 |
rs780642173 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132875364 | ACGCACATTCTGGCC[A/G]GGTGTGGGGGCTCAC | 55743 |
rs780655269 | snp | C/T | 1.65176e-05 | 0.00287376 | missense | CHFR | GRCh38.p7 | 12:132847085 | GAGCCACGAGGCTCT[C/T]GGTCAACATGTTTTT | 55743 |
rs780669678 | snp | C/G | 1.64901e-05 | 0.00287137 | intron-variant | CHFR | GRCh38.p7 | 12:132856458 | GCTCTGAGCCAGGGG[C/G]ATGATTTACCTAATG | 55743 |
rs780706994 | snp | C/G/T | 0.000116059 | 0.00761691 | intron-variant | CHFR | GRCh38.p7 | 12:132856724 | GCGTGCGCAGTGCTG[C/G/T]GGAAGGAGGGGTCTG | 55743 |
rs780721649 | snp | A/G | 1.75696e-05 | 0.00296386 | missense | CHFR | GRCh38.p7 | 12:132857551 | AACGTGTGCATGCAG[A/G]GCTGCAAACTGAAAG | 55743 |
rs780730358 | snp | A/C | | | intron-variant | CHFR | GRCh38.p7 | 12:132864089 | TTACAGGTGTGAATA[A/C]CCTATATCTTAATAA | 55743 |
rs780753816 | snp | A/G | 1.68812e-05 | 0.00290522 | intron-variant | CHFR | GRCh38.p7 | 12:132847175 | AATACTCGTTTAGAG[A/G]AAGAAACACTGAAAT | 55743 |
rs780851344 | in-del | -/CCAGCAACA | | | intron-variant | CHFR | GRCh38.p7 | 12:132844157 | AACACAGCCAGTTAC[-/CCAGCAACA]CCAGCAACACCATCT | 55743 |
rs780860591 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132842320 | CTACTGAAAACTGTC[C/T]GCCAGTCAACAGTGA | 55743 |
rs780919643 | snp | G/T | 3.91535e-05 | 0.00442439 | missense, upstream-variant-2KB | CHFR, LOC101928530 | GRCh38.p7 | 12:132887324 | CCTTCCTCGGGCCGC[G/T]CCATCGGGATTCACA | 55743 |
rs780923793 | snp | C/T | 9.3314e-05 | 0.00682996 | missense, intron-variant | CHFR | GRCh38.p7 | 12:132869759 | GACGACGGAGGGACC[C/T]GGGGATCGGCCCCTC | 55743 |
rs780945230 | snp | A/C/G | 4.94395e-05 | 0.00497169 | missense | CHFR | GRCh38.p7 | 12:132861571 | GCTGAGGCAAAGCTG[A/C/G]AGACTTCATCACTTG | 55743 |
rs780945785 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132849230 | CTAGGATTACAGGCA[C/T]GATGCACTGCGCCCG | 55743 |
rs781010571 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132870339 | CCTGGGCGACAAAGC[A/G]CGACTCCATCTCAAA | 55743 |
rs781023292 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132882093 | CTACAAAGACTGCAC[A/G]CTTATGTTTATATTA | 55743 |
rs781034479 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132859483 | AGCCTCCTGAGTAGC[C/T]GGGACTACAGGTGCC | 55743 |
rs781035012 | snp | A/G | 1.6588e-05 | 0.00287988 | intron-variant | CHFR | GRCh38.p7 | 12:132861457 | AGGACACACACAACC[A/G]GACACTAACCTCCTC | 55743 |
rs781107351 | snp | C/G | 1.66396e-05 | 0.00288436 | missense | CHFR | GRCh38.p7 | 12:132877598 | ATTTTTCATCCACTA[C/G]AATTCTACAGTGATC | 55743 |
rs781121506 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132871313 | AAAAATTAGCCGGGT[A/G]TGGTGGTGTGCACCT | 55743 |
rs781133343 | snp | A/C | 1.72104e-05 | 0.00293341 | intron-variant | CHFR | GRCh38.p7 | 12:132843986 | GCCAAGAAGCCAACC[A/C]AGACAGAACTAGAGC | 55743 |
rs781181121 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132870455 | AGAATCTCTCGAACC[C/T]GGCAGGAGGAGGCTG | 55743 |
rs781209351 | in-del | -/AAA | 1.66102e-05 | 0.00288181 | intron-variant | CHFR | GRCh38.p7 | 12:132847140 | GTAATTCTGTGACGC[-/AAA]AAAAGAGAGGAATAA | 55743 |
rs781220656 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132867566 | AACAGCAGCGTGGAG[C/T]GCACAGAAGGCCCTG | 55743 |
rs781224248 | snp | A/C/G | 0.000100275 | 0.00708014 | synonymous-codon | CHFR | GRCh38.p7 | 12:132851667 | CTCCGCTCTCCGGTC[A/C/G]GGCATGGGCTGGAAG | 55743 |
rs781249933 | snp | A/G | 1.66994e-05 | 0.00288953 | intron-variant | CHFR | GRCh38.p7 | 12:132848730 | CAGACCGCACCTGTG[A/G]AGAGAGGACACTCGT | 55743 |
rs781356013 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132885614 | ATATTTTCTCTCCTT[C/G]TCTTAACATGTAATG | 55743 |
rs781395404 | snp | G/T | 1.64811e-05 | 0.00287059 | missense | CHFR | GRCh38.p7 | 12:132859171 | CCTCGTGGACGGTTT[G/T]GGCATTTCTACGCGG | 55743 |
rs781395671 | snp | A/T | 1.71962e-05 | 0.0029322 | intron-variant | CHFR | GRCh38.p7 | 12:132872431 | ATTTATTCTACTTAA[A/T]ATAACTTGGAGTTAC | 55743 |
rs781424137 | snp | C/T | 6.74536e-05 | 0.00580709 | intron-variant | CHFR | GRCh38.p7 | 12:132857376 | CCGCCCTCACGTGCC[C/T]GGGTGCTGGTGTGGA | 55743 |
rs781451957 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132848214 | GCAGGAAAGCACTGT[C/G]TGCCCGACACTGAGG | 55743 |
rs781479536 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132866869 | AACAACGTCTCTACT[A/G]AAAATACAAAAATTT | 55743 |
rs781511228 | snp | A/G | 9.94827e-05 | 0.00705205 | synonymous-codon | CHFR | GRCh38.p7 | 12:132853447 | TGTCGTCAGGCTGAC[A/G]GACGTGGAGGGTGCA | 55743 |
rs781543889 | snp | A/G | | | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132841234 | TTTAACTGTAGTTTC[A/G]GAAAATGTACAAAAG | 55743 |
rs781614371 | snp | A/G | 1.65146e-05 | 0.0028735 | missense | CHFR | GRCh38.p7 | 12:132847072 | ACTCCCCGCTGGAGA[A/G]CCACGAGGCTCTCGG | 55743 |
rs781699438 | snp | A/G | 4.0744e-05 | 0.00451335 | missense | CHFR | GRCh38.p7 | 12:132853544 | TGCCTTCTGTACTCA[A/G]GACACTGCCGGCACA | 55743 |
rs781748631 | snp | G/T | 1.66101e-05 | 0.0028818 | missense | CHFR | GRCh38.p7 | 12:132859214 | CAACTGCCCGTTCAG[G/T]TCAAGGTCCCCATCT | 55743 |
rs796139459 | snp | C/G | | | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132840788 | CCGCGGTCACTCACA[C/G]AAGGGAGCAGCATGT | 55743 |
rs796185244 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132882269 | GGGAAAGAAGCCAGG[C/T]GCAGAAGATGATGGC | 55743 |
rs796201985 | snp | A/T | | | synonymous-codon | CHFR | GRCh38.p7 | 12:132861591 | TTCATCACTTGCCAC[A/T]GAGGGACCACTTCCT | 55743 |
rs796217445 | in-del | -/AC | | | intron-variant | CHFR | GRCh38.p7 | 12:132864187 | ATTTGAAAAAAAAAA[-/AC]ACAAGAAACTGGCTT | 55743 |
rs796230830 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132880815 | ACTAAAAATACAAAA[C/T]TTAGCCAGGCATGGT | 55743 |
rs796281205 | snp | C/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132862512 | AGGAGGCTGAGGTGA[C/G]TGGATCACTTGAGCC | 55743 |
rs796378602 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132849650 | GCCTAGGCTGGAGTA[C/T]AGTGGAGCAATCTCG | 55743 |
rs796475139 | in-del | -/TT | | | intron-variant | CHFR | GRCh38.p7 | 12:132867958 | GAATAGCTAAGAAAA[-/TT]AAAAAAAAATAATAT | 55743 |
rs796479790 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132879414 | TTTTTTTTTTGAGAC[A/G]GAGTCTCTTTCTGTG | 55743 |
rs796480955 | in-del | -/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132852147 | GCCACGCCTGGCTAA[-/T]TTTTTTTTTTTTTTG | 55743 |
rs796532119 | in-del | -/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132882719 | AGGTTTTTTTTTTTT[-/T]CTTTGAGACAAGGCC | 55743 |
rs796574941 | multinucleotide-polymorphism | GG/TC | | | utr-variant-3-prime | CHFR | GRCh38.p7 | 12:132841339 | GCCCTGCCCAGCGCT[GG/TC]CCAGGAGGGCGGGCT | 55743 |
rs796667828 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132884335 | GAGGCAGGAGAATTG[C/T]TTGAACCCGGGAGGT | 55743 |
rs796672357 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132876070 | AATGCCAGCTACTCG[A/G]GAGGCTGGGGCAGGA | 55743 |
rs796775262 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132855895 | TAAATATCATGGCCT[C/T]GACCCAACATTCAGA | 55743 |
rs796789788 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132851218 | CTGGTCTGAAACTCC[C/T]GGACACAGAAGATCC | 55743 |
rs796876633 | in-del | -/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132855862 | TCAAGTGTTTTTTTT[-/T]GTCGTTCATTGTCTT | 55743 |
rs796892663 | snp | A/G | | | intron-variant | CHFR | GRCh38.p7 | 12:132876077 | GCTACTCGGGAGGCT[A/G]GGGCAGGAGAATGGC | 55743 |
rs796896883 | snp | C/T | | | intron-variant | CHFR | GRCh38.p7 | 12:132857764 | AAAGACAGAGGCGAG[C/T]AGATTATGACTTCAG | 55743 |
rs796999989 | in-del | -/TAAA | | | intron-variant | CHFR | GRCh38.p7 | 12:132867959 | AATAGCTAAGAAAAT[-/TAAA]AAAAAATAATATGTA | 55743 |