SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs73040915 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | RFWD2 | GRCh38.p7 | 1:176064653 | ACGGTTTCTTTCCCC[G/T]TTTTCTTTCTTTTTT | 64326 |
rs73040918 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | RFWD2 | GRCh38.p7 | 1:176067298 | CCAGGCCTGTGCCCA[C/T]GGACTAAGGTGAGGA | 64326 |
rs73040923 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | RFWD2 | GRCh38.p7 | 1:176073444 | ACAAAATTCAAACTC[A/G]GAATTCAAAAGACAA | 64326 |
rs73040924 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | RFWD2 | GRCh38.p7 | 1:176073859 | TATGTCATGCAATTT[A/T]ACAGTAAGAATAATT | 64326 |
rs73040925 | snp | C/T | 0.160938 | 0.233598 | intron-variant | RFWD2 | GRCh38.p7 | 1:176074227 | CCACCTCACCTGGCC[C/T]CTTTATTCCTCTTTC | 64326 |
rs73040940 | snp | G/T | 0.177182 | 0.23916 | intron-variant | RFWD2 | GRCh38.p7 | 1:176094122 | AATAATCAGGAACAG[G/T]GCATATAAAACAAAT | 64326 |
rs73040946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176101841 | GACAGGCCTCTCAGG[A/G]AGATCTGACTGCCAT | 64326 |
rs73040951 | snp | A/G | 0.195837 | 0.244062 | intron-variant | RFWD2 | GRCh38.p7 | 1:176104663 | TTTCAAAGTCATTCT[A/G]TTAGAGGTGCTGTGG | 64326 |
rs73042718 | snp | A/C | 0.177182 | 0.23916 | intron-variant | RFWD2 | GRCh38.p7 | 1:176107974 | GTACCAATTTAGAGG[A/C]GATTAAAGAGACATG | 64326 |
rs73042723 | snp | C/G | 0.177182 | 0.23916 | intron-variant | RFWD2 | GRCh38.p7 | 1:176110570 | GGAAACTTCATTATA[C/G]CAAGGATTACTATCT | 64326 |
rs73042728 | snp | A/G | 0.177503 | 0.239258 | intron-variant | RFWD2 | GRCh38.p7 | 1:176114597 | TTTTTGCGGGGGGAG[A/G]GAGTGGGGGGGAAAG | 64326 |
rs73042736 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | RFWD2 | GRCh38.p7 | 1:176119906 | GGCACTGAGAGATTA[C/T]ATATGTGGCCCAAGA | 64326 |
rs73042741 | snp | A/G | 0.177182 | 0.23916 | intron-variant | RFWD2 | GRCh38.p7 | 1:176127709 | TGAATAATGGGACAA[A/G]GAAGATGGGACTTTT | 64326 |
rs73042743 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | RFWD2 | GRCh38.p7 | 1:176134847 | GGCATGAAATCCAAC[A/G]CATTAAGGAAACAGA | 64326 |
rs73042749 | snp | C/T | 0.177182 | 0.23916 | intron-variant | RFWD2 | GRCh38.p7 | 1:176141072 | TGACTTTCATTAGTG[C/T]CTTGATAAAGATATG | 64326 |
rs73042786 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176191384 | ATACTCAAATTTATA[C/T]ACAACTTCAAGAATG | 64326 |
rs73042795 | snp | C/T | 0.196771 | 0.244268 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207398 | CGAAGGGAGTCTGTC[C/T]GTCCCAAGCCGCTTT | 64326 |
rs74127150 | snp | C/T | 0.166832 | 0.235761 | intron-variant | RFWD2 | GRCh38.p7 | 1:175955808 | CACACACACGGCCTA[C/T]ATACTAAAAATTACC | 64326 |
rs74127154 | snp | A/T | 0.166832 | 0.235761 | intron-variant | RFWD2 | GRCh38.p7 | 1:175980952 | CACATAGGAACAAAT[A/T]TATTCATTTGTATAC | 64326 |
rs74127162 | snp | C/T | 0.105924 | 0.204309 | intron-variant | RFWD2 | GRCh38.p7 | 1:176029183 | TTAAGAATTTCATGA[C/T]TTTAAATTTTTATGT | 64326 |
rs74127164 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176033931 | CACAAAGGCAATATT[G/T]TATATGATCGCCAAA | 64326 |
rs74127167 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | RFWD2 | GRCh38.p7 | 1:176047157 | AGTTGAAATGAATCA[C/T]CACATACATTATTCC | 64326 |
rs74127169 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:176054722 | TCCTGTATCAATCAA[A/T]TTTTCCATCTATCCT | 64326 |
rs74127185 | snp | C/T | 0.173444 | 0.23926 | intron-variant | RFWD2 | GRCh38.p7 | 1:176135628 | CTTAGACTCTAATTT[C/T]TGATCAGTAATCCAG | 64326 |
rs74127188 | snp | A/G | 0.194902 | 0.243853 | intron-variant | RFWD2 | GRCh38.p7 | 1:176148495 | TAGTGTGAAATGACT[A/G]AGAAATTTTATAAAT | 64326 |
rs74127189 | snp | A/G | 0.194902 | 0.243853 | intron-variant | RFWD2 | GRCh38.p7 | 1:176148496 | AGTGTGAAATGACTG[A/G]GAAATTTTATAAATG | 64326 |
rs74127190 | snp | C/T | 0.160609 | 0.233472 | intron-variant | RFWD2 | GRCh38.p7 | 1:176149274 | TAAAACTAACTAAAA[C/T]TAAGAAACAGGTGTT | 64326 |
rs74127192 | snp | A/G | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176151326 | GAAAGAAAGAAGGAA[A/G]GAAAGAAAGAAGGAA | 64326 |
rs74127194 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176151910 | GTACAGTTCACTCTA[C/G]AACAGTTGTCTCAAG | 64326 |
rs74127200 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176183369 | ATGCCAACAGAATAG[A/C/G]TTTAAAAATAAGCAA | 64326 |
rs74263829 | in-del | -/AA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176148407 | TTAAAAAAAAAAAAA[-/AA]GTTTTCAAAGTTATT | 64326 |
rs74316015 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:176136802 | TTTGATTTTACAATA[A/G]AAGTATGAGATGAAT | 64326 |
rs74317402 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176076551 | TTAATGACCTTACAT[C/T]ACATGTAGAGGAACT | 64326 |
rs74337983 | snp | A/C | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176091346 | GCGAGACTCCGTCTC[A/C]AAAAAAAAAAAACAA | 64326 |
rs74341821 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176176465 | AAACCATCATCTTCA[C/G]GAGTCACAAAAAGCT | 64326 |
rs74387136 | snp | C/T | 0.084364 | 0.187256 | intron-variant | RFWD2 | GRCh38.p7 | 1:175959605 | GAGAGTTTAGCAAGA[C/T]GGTTGGATTAAAAAT | 64326 |
rs74410932 | snp | G/T | 0.0898077 | 0.191933 | intron-variant | RFWD2 | GRCh38.p7 | 1:176159915 | ACATACGCCAAAATC[G/T]TCACATTTATTAAAA | 64326 |
rs74413814 | snp | A/G | 0.0689305 | 0.172377 | intron-variant | RFWD2 | GRCh38.p7 | 1:176134157 | AGTGATAAGGTTTCC[A/G]AAGGTTATTATAATC | 64326 |
rs74417768 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176169089 | AGGCAAAGAAATGAG[A/T]CATGTTGCTGTAAAA | 64326 |
rs74421691 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175999333 | TTTCATTTTTAGATC[A/C]CACAAATAAGTGAGA | 64326 |
rs74439428 | snp | A/C | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176036517 | AAAAACAAAAAAAAA[A/C]AAAAAAAAAGCATGG | 64326 |
rs74456404 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | RFWD2 | GRCh38.p7 | 1:176017352 | GATGCTTGAGAGTTT[A/G]TAAAAGTCCTCAATG | 64326 |
rs74457605 | snp | C/T | 0.093417 | 0.194889 | intron-variant | RFWD2 | GRCh38.p7 | 1:176036819 | GGTTAGGCTAAGCTA[C/T]GATTAGAAGTATTAA | 64326 |
rs74511988 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176168682 | GAATCAGCCTTTCAG[A/G]ATCAGGAGAGGGAAA | 64326 |
rs74544018 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176015296 | ACAAGTAGAGAAGAG[C/T]TGAGTATTCAGGCAA | 64326 |
rs74545179 | snp | A/C | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992946 | TTGGGGTCAGCGACC[A/C]ACTTGAGGAGGCAGT | 64326 |
rs74554321 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176035325 | GAAGGAATCATGAGC[G/T]AGAAGACAGAACAAT | 64326 |
rs74557986 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:176156977 | CCAAGGCAGGCAGAT[C/T]ACCCAAGGCCAGGAG | 64326 |
rs74644786 | snp | A/C | 0.0333695 | 0.124785 | intron-variant | RFWD2 | GRCh38.p7 | 1:176001986 | TCTTAATGAGGATCC[A/C]TGGTACTTGCTGAGC | 64326 |
rs74659647 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | RFWD2 | GRCh38.p7 | 1:176077213 | TCATAAACACAGATA[C/T]AAAAATCCTCGACAA | 64326 |
rs74660627 | snp | G/T | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:175947387 | TTTTTTTTTTTTTTT[G/T]TGAGACGGAGTCTTG | 64326 |
rs74680409 | snp | C/T | 0.100944 | 0.200705 | intron-variant | RFWD2 | GRCh38.p7 | 1:176046856 | ACTGAATTATCATTA[C/T]TTTTCCCCAAATCCA | 64326 |
rs74686701 | snp | A/G | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176195118 | AAAGGAGAGGAGAGA[A/G]AGAGGGAGAGGAGAG | 64326 |
rs74693299 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | RFWD2 | GRCh38.p7 | 1:175972096 | CTTAACAAAACAAAA[A/G]GAGAGAATTATGTAA | 64326 |
rs74728598 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176106978 | TGGTGACAAAGCAAT[G/T]CCGGTGCAACCTAGC | 64326 |
rs74771610 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | RFWD2 | GRCh38.p7 | 1:176181929 | ATTATAATAAGGATC[A/T]AAGCCTAAATTGTTT | 64326 |
rs74782633 | snp | C/T | 0.021333 | 0.101051 | intron-variant | RFWD2 | GRCh38.p7 | 1:176182412 | CTCAAGGGAGGAAAA[C/T]TTTGTCCCCCAAGGG | 64326 |
rs74863020 | snp | C/T | 0.107694 | 0.205546 | intron-variant | RFWD2 | GRCh38.p7 | 1:176193475 | ATACACAAATGTTCA[C/T]GGGAACATTATTCAT | 64326 |
rs74893783 | snp | A/C | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176100394 | ACTTTGTCTCAAAAA[A/C]AAAAAAAAAAAAAAA | 64326 |
rs74911799 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176149457 | AATCACTTTCTCCAT[C/G]AGAAGTTCATTTGCA | 64326 |
rs74915680 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176056442 | ACACAGGGATTTTTT[A/T]ATATATAAAGATACT | 64326 |
rs74920227 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175982049 | GCAAGAATGTGGAGA[A/G]AAGAGAACTCTTGTA | 64326 |
rs74943188 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | RFWD2 | GRCh38.p7 | 1:176037105 | ATTCTACCAAACATT[C/T]AAGAACAAAAGAATA | 64326 |
rs74961189 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176048354 | CAATTTAAAAAAAAA[A/G]TTTATTCAGTTAAGT | 64326 |
rs74977377 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | RFWD2 | GRCh38.p7 | 1:176167721 | AGAGGCAGAACAGTA[C/T]AGTAAAAGCACAGAT | 64326 |
rs74985738 | snp | A/G | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176094687 | TTAAAAAAAAAAAAA[A/G]GTCCTCAAATAAATG | 64326 |
rs74986818 | snp | A/T | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176179874 | GACAAAAAAAAAAAA[A/T]ATGGGACATAGCTGG | 64326 |
rs75011270 | snp | A/G | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176095697 | AAAAAAAAAAAAAAA[A/G]AGATGTTCTTTGCAA | 64326 |
rs75015620 | snp | A/C | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176036518 | AAAACAAAAAAAAAA[A/C]AAAAAAAAGCATGGC | 64326 |
rs75023849 | snp | C/T | 0.0998734 | 0.199905 | intron-variant | RFWD2 | GRCh38.p7 | 1:175980580 | AATTTGGAAATCTGT[C/T]ATCCTGATCCCTGCC | 64326 |
rs75035453 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176094380 | AAATTATAAATAATA[A/T]TAATATAAAAAATAG | 64326 |
rs75078139 | snp | C/T | 0.0894459 | 0.191631 | intron-variant | RFWD2 | GRCh38.p7 | 1:176190253 | TTAAAATCCAAAATG[C/T]CCCAATAAGTATTTT | 64326 |
rs75084819 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | RFWD2 | GRCh38.p7 | 1:176119577 | AGGTATAATGCAGGC[C/T]ACAATAGAAAAATTT | 64326 |
rs75122522 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | RFWD2 | GRCh38.p7 | 1:176048389 | CTGACTAGGGCACAA[C/T]TCAGCAAATGTTCCC | 64326 |
rs75123029 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176082156 | TTTCAGCACTGTGTC[A/G]TTTGAACATATACTT | 64326 |
rs75124417 | snp | C/G/T | 0.00514594 | 0.0504634 | intron-variant, missense, utr-variant-5-prime | RFWD2 | GRCh38.p7 | 1:176136495 | TTCCTTACTTCCACT[C/G/T]TCTTAATATCCTCTT | 64326 |
rs75137212 | snp | A/T | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:175950229 | TAAAAAAAAAAAAAG[A/T]CAACATACGAATTGA | 64326 |
rs75137556 | snp | C/T | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992948 | GTCAGGGGTCAGGGA[C/T]CCACTTGAGGAGGCA | 64326 |
rs75139804 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:176182749 | GAAAAGGCCAAGACC[A/G]TACCTGTATCAGCCC | 64326 |
rs75154054 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176076926 | CAAACAATAAGAAAG[C/T]GAAAATCTGAACTGA | 64326 |
rs75161807 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | RFWD2 | GRCh38.p7 | 1:176000276 | GACTTGATTTTCATA[C/T]ATGGTGACAGACAGA | 64326 |
rs75162337 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176174092 | ACTCATATATAACTC[A/T]CTCTCACTATTTAGA | 64326 |
rs75172992 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | RFWD2 | GRCh38.p7 | 1:176110171 | CAACCAATTTTTCGA[A/T]ATTCTCCAAGGATTA | 64326 |
rs75220395 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | RFWD2 | GRCh38.p7 | 1:176187875 | GTTCTCCCAAATTTC[A/G]TATGTTGAAATCTTA | 64326 |
rs75223798 | snp | A/C | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176203337 | GCGAGACTCCGTCTC[A/C]AAAAAAAAGAAAAAA | 64326 |
rs75224169 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | RFWD2 | GRCh38.p7 | 1:176161744 | GGCAAACAGTAGATG[C/T]TAATAGTAAACTATG | 64326 |
rs75231100 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176159957 | TATTTCAGAGCCCCA[C/T]ATTATTTTCTGTACT | 64326 |
rs75248386 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176166565 | TAAATTCTACATTTA[A/C]CAAACGAAGTTTTTT | 64326 |
rs75261414 | snp | C/T | 0.0333238 | 0.124705 | intron-variant | RFWD2 | GRCh38.p7 | 1:176198759 | AAAGAACACTTACAA[C/T]GCAAGATGACATGCA | 64326 |
rs75265287 | snp | A/C | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:175949176 | TCCGTCTCAAAAAAA[A/C]AAAAAAAAAAAAAAA | 64326 |
rs75267413 | snp | C/G | 0.0704125 | 0.17392 | intron-variant | RFWD2 | GRCh38.p7 | 1:175999624 | TCTGTTGGGTATATA[C/G]CCAGCAGTGGGACTG | 64326 |
rs75280872 | snp | C/T | 0.0566069 | 0.158427 | intron-variant | RFWD2 | GRCh38.p7 | 1:175961172 | CTCCCTGGCATATCA[C/T]GGTATGTCTCACCCT | 64326 |
rs75285433 | snp | C/T | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176152462 | TAGATTTTTTTTTTT[C/T]CTTGAGACAGAGCCT | 64326 |
rs75288311 | snp | A/C | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176019861 | GGGAGAATCCTGTCT[A/C]AAAAAAAAAATCACT | 64326 |
rs75288399 | snp | C/T | 0.021333 | 0.101051 | intron-variant | RFWD2 | GRCh38.p7 | 1:176129401 | AGCACAGAAAATAGG[C/T]AATTCAGGATTCAAA | 64326 |
rs75293565 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | RFWD2 | GRCh38.p7 | 1:176045488 | TTGAAAATGTTCAAA[A/G]TTCTATACAAAGTTA | 64326 |
rs75319172 | snp | A/C | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:175963932 | ATTGCACAATATTTG[A/C]TGAACTAAAAACAAG | 64326 |
rs75356767 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | RFWD2 | GRCh38.p7 | 1:175977511 | CTGATGTCAACCCTG[A/G]TAGCTTTATTTGGGA | 64326 |
rs75388602 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | RFWD2 | GRCh38.p7 | 1:175945736 | GAAGCAAATGGCTAA[C/G]AAAGATCACGGAACA | 64326 |
rs75489782 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | RFWD2 | GRCh38.p7 | 1:176036596 | ATTTAAATAGCTCAA[C/T]TTATGATTTTTTGAC | 64326 |
rs75508062 | snp | A/T | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176122156 | AAAAAAAAAAAAAAA[A/T]ATCTGGGCTCAAAAA | 64326 |
rs75520133 | snp | A/C/T | 0.00676609 | 0.0577691 | intron-variant | RFWD2 | GRCh38.p7 | 1:175955375 | CCTATGAAAAACTTA[A/C/T]AACTAACATCATACT | 64326 |
rs75569726 | snp | A/C | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176062851 | TGGGCAGCAACATCA[A/C]TGAATCTCAAAAACA | 64326 |
rs75607477 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176132270 | ACTTTCCATCATAAT[C/T]AGTCTTTACTTGATT | 64326 |
rs75633268 | snp | A/G | 0.084364 | 0.187256 | intron-variant | RFWD2 | GRCh38.p7 | 1:176039749 | CAGAGAAAGACTAAA[A/G]ATAAACTCTTGCATA | 64326 |
rs75649913 | snp | A/C | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176088996 | GCAAAACTCAGTCTC[A/C]AAAAAAAAAAAAAAA | 64326 |
rs75670509 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176134955 | CCTAAAGGACTAGAC[A/C]ATATGCATACTTTGT | 64326 |
rs75697563 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | RFWD2 | GRCh38.p7 | 1:176098454 | AAAAGTTTAACAGAG[C/T]GAGACTCCATCTCAA | 64326 |
rs75721919 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | RFWD2 | GRCh38.p7 | 1:176125993 | CTTTATAAATAAGAA[C/T]ATATTTTTATTCTTT | 64326 |
rs75731074 | snp | A/C | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176142718 | ACAGAAATCCAGAAC[A/C]AAAAAAAAACAAAAT | 64326 |
rs75737216 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | RFWD2 | GRCh38.p7 | 1:176152735 | GTGAGCCACTGTGCC[C/T]AGCTTAAAATTCTAA | 64326 |
rs75741165 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RFWD2 | GRCh38.p7 | 1:175953485 | ACTTTAGGCTGGGCG[C/T]GGTGGCTCATGCCTG | 64326 |
rs75741442 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176014396 | CACAAGTTATGCTGC[C/T]TAGTTGCAACCTTTA | 64326 |
rs75748826 | snp | C/T | 0.040671 | 0.13668 | intron-variant | RFWD2 | GRCh38.p7 | 1:175965363 | TCTTAAATTTTTCTT[C/T]GTTCAACGCCTTGTT | 64326 |
rs75759749 | snp | A/G | 0.089084 | 0.191327 | intron-variant | RFWD2 | GRCh38.p7 | 1:176183484 | TGTGGAAAAATTGGA[A/G]CTCTTATGCACTGTT | 64326 |
rs75771887 | snp | A/G | 0.0123952 | 0.0777428 | intron-variant | RFWD2 | GRCh38.p7 | 1:176163025 | ACACAACAACTTCCT[A/G]TGAAGACTGTTTTAG | 64326 |
rs75802192 | snp | A/G | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176173327 | AAAAAACAAAATGAA[A/G]AAAAAAAAAAAAAAA | 64326 |
rs75803805 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176200348 | AATATCTAAAAGAAC[A/C/T]CCCAAAACAGTCGTA | 64326 |
rs75804516 | snp | A/C | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176149863 | AATAAGAGACAGTTT[A/C]TGAACAAACATCATT | 64326 |
rs75818964 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | RFWD2 | GRCh38.p7 | 1:176187921 | TTAAAACATGGGCCT[C/T]TGGGAGATTTTTAGG | 64326 |
rs75858053 | snp | G/T | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:175977966 | TATGAAAATTTGGTA[G/T]GGATTACCAAAAGAT | 64326 |
rs75860432 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | RFWD2 | GRCh38.p7 | 1:176114127 | TAGCTATAAATGCCA[A/G]GCCAGTTTCCAGATA | 64326 |
rs75865782 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | RFWD2 | GRCh38.p7 | 1:176010333 | ATTGATATAATATAC[A/G]ATGCATCCTATATTC | 64326 |
rs75867466 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176146685 | CTTAATTGCAGCTTG[G/T]TAAGAAACCCAGAGC | 64326 |
rs75880053 | snp | C/T | 0.0452528 | 0.143452 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176184989 | TTTTTAGTAGTACAA[C/T]GCAGTCACCAGAGCC | 64326 |
rs75880882 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176058853 | AACACGCCTCCTCAG[A/T]TCCCATATGTGAGTT | 64326 |
rs75880956 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:176189438 | GAGAAACAAAAATAC[A/T]TCTTTAAAATACTAA | 64326 |
rs75893458 | snp | A/C/T | 0.00954224 | 0.0684493 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176176960 | TAAGGTTTTTACATA[A/C/T]CCTTTTGAATATTTT | 64326 |
rs75911432 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | RFWD2 | GRCh38.p7 | 1:176065025 | TTAGAGAGACACAAA[C/T]CATATAACTAAGATT | 64326 |
rs75916161 | snp | C/G | 0.0356815 | 0.128715 | intron-variant | RFWD2 | GRCh38.p7 | 1:176136940 | TTTAAATAGAGATAG[C/G]TTTCACTATGTTGCC | 64326 |
rs75952752 | snp | C/T | 0.106278 | 0.204558 | intron-variant | RFWD2 | GRCh38.p7 | 1:176002570 | GTCCATGTGATCTCA[C/T]TGTTCAATTCCCACC | 64326 |
rs75979890 | snp | A/T | 0.250168 | 0.25 | intron-variant | RFWD2 | GRCh38.p7 | 1:176014592 | AAATACATGTTTTTT[A/T]AAAAATTAAAATCTA | 64326 |
rs75997117 | snp | G/T | 0.093777 | 0.195178 | intron-variant | RFWD2 | GRCh38.p7 | 1:176170587 | ACGATATTCAGTAAA[G/T]CACGCTGAAAAGAGA | 64326 |
rs76014509 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175973771 | CACTCTAATATTTTT[G/T]TGGCTACAAAACTCA | 64326 |
rs76105168 | snp | A/C | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176173637 | AGTGGGGCGCTGTCT[A/C]AAAAAAAAAAAAAAA | 64326 |
rs76105433 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175950770 | GACAACAGAAAAATT[A/C]GCAAGTCTTTTATAA | 64326 |
rs76108440 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176108391 | TTCCAGAATTTTTGC[A/G]CATATGATTAATACC | 64326 |
rs76127056 | snp | A/G | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176023739 | AAAAAAAAAAAAAAA[A/G]GAAAAGAAAAGAAAA | 64326 |
rs76201789 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | RFWD2 | GRCh38.p7 | 1:175954177 | ATTTGCAAATTTAAA[A/G]ATATACTCCCAAATA | 64326 |
rs76208718 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | RFWD2 | GRCh38.p7 | 1:175948378 | GTCATAGAGGTCAGG[C/T]CAGGTGGCAGAGAGA | 64326 |
rs76230206 | snp | G/T | 0.021333 | 0.101051 | intron-variant | RFWD2 | GRCh38.p7 | 1:176059471 | TGTAGTTAGGGAGTT[G/T]GCAAAATCTTTTTTC | 64326 |
rs76244594 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176164098 | ACAACTACTATTACT[A/G]TAGGAGAATTCTTCA | 64326 |
rs76252831 | snp | A/T | 0.108048 | 0.20579 | intron-variant | RFWD2 | GRCh38.p7 | 1:176166857 | TGGTAGGACTGCCTG[A/T]GCTCAGGAGTTCGAG | 64326 |
rs76258996 | snp | G/T | 0.0217236 | 0.101931 | intron-variant | RFWD2 | GRCh38.p7 | 1:176071604 | AGGATCACAGAAAGA[G/T]TTTCTAAATAAAATG | 64326 |
rs76266964 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176190785 | CTGTCCAACAAACTA[A/C]TATGTACATAGTTCA | 64326 |
rs76286821 | snp | C/G | 0.093777 | 0.195178 | intron-variant | RFWD2 | GRCh38.p7 | 1:176012663 | AAGTGCTCTATAAAG[C/G]TGTACCATTTTTTTT | 64326 |
rs76291782 | snp | C/T | 0.146985 | 0.227789 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176145725 | TTCAGCCGAAGAAGA[C/T]AGGAATAAAAGATTA | 64326 |
rs76302824 | snp | A/C | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176019862 | GGAGAATCCTGTCTC[A/C]AAAAAAAAATCACTA | 64326 |
rs76309149 | snp | A/C | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176091345 | AGCGAGACTCCGTCT[A/C]AAAAAAAAAAAAACA | 64326 |
rs76343768 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:176124664 | TTTTCTCAATTCATT[C/T]ATCTGTTGATGGACA | 64326 |
rs76409321 | snp | A/G | 0.0898077 | 0.191933 | intron-variant | RFWD2 | GRCh38.p7 | 1:176157306 | GCAAGTGGAATATTT[A/G]CAAAACAGATTATGC | 64326 |
rs76431299 | snp | A/G | 0.0170251 | 0.090679 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175969453 | CTTACCTGAGGAAAG[A/G]AATGCCCTTATCTCT | 64326 |
rs76438230 | snp | A/T | 0.0452528 | 0.143452 | intron-variant | RFWD2 | GRCh38.p7 | 1:176157415 | GTAAAAGGGACTAGA[A/T]TTACATTCCTGCCTT | 64326 |
rs76449118 | snp | A/G | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176120445 | AAAATAAAAAAAAAA[A/G]GCTTAATAAAGACAT | 64326 |
rs76453178 | snp | A/G | 0.093417 | 0.194889 | intron-variant | RFWD2 | GRCh38.p7 | 1:176053226 | CCCAGCTCTCCCCTG[A/G]ATATACTGCTTCCTC | 64326 |
rs76454857 | snp | A/T | 0.0425829 | 0.139564 | intron-variant | RFWD2 | GRCh38.p7 | 1:176193027 | ACACAAAATGCATTC[A/T]AACAGTGAAAATATG | 64326 |
rs76464973 | snp | A/G | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:175950227 | GTTAAAAAAAAAAAA[A/G]GTCAACATACGAATT | 64326 |
rs76593336 | snp | C/T | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176118349 | GTCTACACAGCAGTC[C/T]TTTTTTTTTAAGGCA | 64326 |
rs76600680 | snp | C/T | 0.093777 | 0.195178 | intron-variant | RFWD2 | GRCh38.p7 | 1:176180920 | CATGCTGGGAGATGA[C/T]GATGCTGAAGGACCC | 64326 |
rs76604110 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | RFWD2 | GRCh38.p7 | 1:175993059 | GTCCTGTTCTCTGAT[C/G]GTTCCTCTGGAAGTT | 64326 |
rs76612520 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176185776 | GTCTCCGCTGGACTT[C/G]ACATTACATGAGAAG | 64326 |
rs76620991 | snp | A/T | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176112237 | CCAAAAAAAAAAAAA[A/T]TTCTGATTGTTTTTC | 64326 |
rs76668392 | snp | C/T | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176070335 | GCCACTTGTGCTGCC[C/T]TTTTTTTTTTTTTTT | 64326 |
rs76674522 | snp | C/G | 0.093777 | 0.195178 | intron-variant | RFWD2 | GRCh38.p7 | 1:176013792 | AAAGCAGTGCTTGCA[C/G]AAAAAATTAAAATTC | 64326 |
rs76692030 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176112360 | GGTACATGTGCACAA[C/T]GTGCAGGTTTGTTAC | 64326 |
rs76712481 | snp | A/G | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992952 | GCTGCTCGGGGGTCA[A/G]GGACCCACTTGAGGA | 64326 |
rs76741448 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | RFWD2 | GRCh38.p7 | 1:175990782 | TCGACCTAAATATAG[C/T]CATTCTACCATTTTT | 64326 |
rs76745365 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | RFWD2 | GRCh38.p7 | 1:176156333 | AGATAAAATGAGATA[A/C]TGAAAACCCAATGAT | 64326 |
rs76746408 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | RFWD2 | GRCh38.p7 | 1:176104558 | CATATGAAAACATAG[C/T]CAATCTCATTTATAA | 64326 |
rs76769524 | snp | C/T | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176199958 | AAACAAAATCAGCCT[C/T]TAAATAAAGGCAAGG | 64326 |
rs76788918 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176043944 | AGTTCACAATCATTA[C/T]TCTGCCCACAACATA | 64326 |
rs76790459 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | RFWD2 | GRCh38.p7 | 1:176174215 | TATATATTTAACCAC[C/T]CCAAAAGAGTAAGTA | 64326 |
rs76807785 | snp | A/G | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176095683 | GACCCTGTCTCAGAA[A/G]AAAAAAAAAAAAAAA | 64326 |
rs76813070 | snp | G/T | 0.0197687 | 0.0974348 | intron-variant | RFWD2 | GRCh38.p7 | 1:176057283 | ATAAGAACTTAAGAG[G/T]GTATTCCCTCCCCAC | 64326 |
rs76847159 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176083067 | TCTCAGGAAATTCCA[A/C]GTATTATAAATAAAA | 64326 |
rs76860240 | snp | A/T | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176050122 | GTATACTTTTGAAAA[A/T]TCGTGTTTCTGGGGA | 64326 |
rs76872562 | snp | C/T | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992963 | GTCCCTGACCCCTGA[C/T]CCCTGAGCAGCCTAA | 64326 |
rs76918602 | snp | A/C | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176173344 | AAAAAAAAAAAAAAA[A/C]CCAGTAATTGGCCAG | 64326 |
rs76925198 | snp | A/C | 0.128288 | 0.218372 | intron-variant | RFWD2 | GRCh38.p7 | 1:176159509 | CCCTAATGCGAGCAC[A/C]AGGAGAAAGGTATAC | 64326 |
rs76935385 | snp | A/T | 0.0356815 | 0.128715 | intron-variant | RFWD2 | GRCh38.p7 | 1:176059391 | ATTTACAAATTAAAA[A/T]CATCTTATTTTCCTT | 64326 |
rs76961681 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:176147269 | TTCAATCTGTCTGCA[C/T]TAAAACATATTTTCT | 64326 |
rs76966776 | snp | G/T | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176063049 | AATTTTTGAAAATGT[G/T]TTTTTTTTTTTTTTT | 64326 |
rs76971890 | snp | A/C | 0.0569829 | 0.158885 | intron-variant | RFWD2 | GRCh38.p7 | 1:176182193 | AAAACCTCACTTCAC[A/C]ATCTATTTCGTATTT | 64326 |
rs76980716 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | RFWD2 | GRCh38.p7 | 1:176127025 | ATAACCATGAGAACA[A/G]GGTTCTAGGGTCTGT | 64326 |
rs76998404 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176095383 | CTATGTTCTTAAAAA[C/T]AGTAAGATGTTATTT | 64326 |
rs77012387 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | RFWD2 | GRCh38.p7 | 1:175976891 | TAACAAGTCTTCTTA[A/G]CAATTAAAAGAAAAA | 64326 |
rs77013499 | snp | A/T | 0.0689305 | 0.172377 | intron-variant | RFWD2 | GRCh38.p7 | 1:176015566 | GTGTGCCTCAAGGTT[A/T]TATCTTGATAACCAA | 64326 |
rs77033416 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | RFWD2 | GRCh38.p7 | 1:176181347 | TGACACAAGAGGCTA[C/T]GGTTAATGACTGAAG | 64326 |
rs77073543 | snp | A/T | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176132173 | AAGGGGTTGAGAGGG[A/T]CACATCTTCTCTGTC | 64326 |
rs77138527 | in-del | -/AA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176036525 | AAAAAAAAAAAAAAA[-/AA]GCATGGCTACAAACC | 64326 |
rs77141540 | snp | A/C | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176091361 | AAAAAAAAAAAAACA[A/C]AAAAAAAAACTTCTG | 64326 |
rs77156197 | snp | A/G | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176045584 | CTTGTTTAGAAGGAA[A/G]AAAAAAAAAAAAAAA | 64326 |
rs77178576 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | RFWD2 | GRCh38.p7 | 1:175958168 | TGTAGTTTATATTTA[C/T]GTAAATTATATTTCA | 64326 |
rs77183828 | snp | C/G | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992939 | CAGGGAAGCACTTGA[C/G]GAGGCTGTCTGCCCG | 64326 |
rs77223325 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | RFWD2 | GRCh38.p7 | 1:176134527 | AGAAGAATTAATAAT[A/C]AGTAGTTATAAGAAA | 64326 |
rs77244876 | snp | A/G | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:175985423 | GGATATTAGCAATCA[A/G]GGGTCACCTCAATTC | 64326 |
rs77326880 | snp | G/T | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176012828 | ATACTATATAGCTTA[G/T]GTATGCAGTAGGTTT | 64326 |
rs77354477 | snp | A/T | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176112239 | AAAAAAAAAAAAAAT[A/T]CTGATTGTTTTTCTT | 64326 |
rs77354627 | snp | C/T | 0.128288 | 0.218372 | intron-variant | RFWD2 | GRCh38.p7 | 1:176068236 | TTCTTCCTTCTCTCC[C/T]TGCCTGCTTTCTTCC | 64326 |
rs77357230 | snp | C/T | 0.093417 | 0.194889 | intron-variant | RFWD2 | GRCh38.p7 | 1:175950565 | TGTGGTCTGCTAGGG[C/T]CTACTATAAATAAGT | 64326 |
rs77361500 | snp | C/G | 0.0930568 | 0.194599 | intron-variant | RFWD2 | GRCh38.p7 | 1:175965188 | CATGTAGGAGGTCAT[C/G]GACTCTGTGTATAGT | 64326 |
rs77417493 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176015824 | ATGATGACAAGAACA[A/C]TTTTAAGTGGAATTA | 64326 |
rs77423753 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176192918 | TTAAGTTTTATTTCA[A/C]AACTACAGTGCTGAA | 64326 |
rs77462811 | snp | A/C | 0.166832 | 0.235761 | intron-variant | RFWD2 | GRCh38.p7 | 1:176041651 | AGCTACCACGCCCGG[A/C]CCCTGCTTGGATTTT | 64326 |
rs77467707 | snp | A/T | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:175961697 | TGAGACCCTGTCTCA[A/T]AAAAAAAAAAAAAAA | 64326 |
rs77469170 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176118055 | CCTCAAAGGTTAAAG[A/C]ATGGGAGGTACTCTA | 64326 |
rs77471071 | snp | A/G | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992909 | GTTCTCAGATCTCCA[A/G]CTGCGTGCTGGGAGA | 64326 |
rs77482080 | snp | C/T | 0.093777 | 0.195178 | intron-variant | RFWD2 | GRCh38.p7 | 1:176096144 | CTGGTTTTAGCTGAA[C/T]TAAGGAGAGAGTTCT | 64326 |
rs77494806 | snp | A/G | 0.0532157 | 0.154195 | intron-variant | RFWD2 | GRCh38.p7 | 1:175985446 | CTCAATTCAATTTCA[A/G]AGATTGATATGAAGT | 64326 |
rs77499776 | snp | C/T | 0.0836354 | 0.186609 | intron-variant | RFWD2 | GRCh38.p7 | 1:176066530 | GGAGATCAAATTTTT[C/T]AAAGTCCAAAACTTC | 64326 |
rs77620619 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | RFWD2 | GRCh38.p7 | 1:176119174 | ATTTTCAGTTTACTC[C/T]ATCCAGAGACTAAGA | 64326 |
rs77666401 | snp | C/T | 0.0894459 | 0.191631 | intron-variant | RFWD2 | GRCh38.p7 | 1:176086032 | ACTGTAATTCTGAGA[C/T]ATTTTCCAATTTATC | 64326 |
rs77666630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176113301 | CCCTGATGGTTAGTG[A/G]TAAGTATTTTTACAT | 64326 |
rs77699026 | snp | C/T | 0.0513262 | 0.151752 | intron-variant | RFWD2 | GRCh38.p7 | 1:176189526 | AGCAAATAAACTCAT[C/T]TTCAAACAAACACAA | 64326 |
rs77702123 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | RFWD2 | GRCh38.p7 | 1:176149731 | ACATTTTCTGAGTAG[C/T]AAAACATAAAAACAC | 64326 |
rs77744924 | in-del | -/AA | 0.105924 | 0.204309 | intron-variant | RFWD2 | GRCh38.p7 | 1:176000348 | CACTGGCATTTATTG[-/AA]AAGACTGTCTTTTCT | 64326 |
rs77750445 | snp | A/C | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176088995 | AGCAAAACTCAGTCT[A/C]CAAAAAAAAAAAAAA | 64326 |
rs77764551 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176195928 | AAAACTGCCTGTTGC[A/G]TACTATGTCCACTAC | 64326 |
rs77776350 | snp | G/T | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176095397 | ATAGTAAGATGTTAT[G/T]TGCAGCCTGGTGTGG | 64326 |
rs77781314 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | RFWD2 | GRCh38.p7 | 1:175962911 | AGTTAATGATTATAT[A/C]CGCAAACATAGTTCA | 64326 |
rs77784162 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:175979817 | TATTAGAAGTATCTC[C/T]CAACTCCACTTCAGC | 64326 |
rs77796178 | snp | A/T | 0.0232847 | 0.105357 | intron-variant | RFWD2 | GRCh38.p7 | 1:175963179 | CCACTGCTATGATAA[A/T]ACTCTCATGGGATTA | 64326 |
rs77798782 | snp | C/T | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:175980683 | CCCTAATGACCACTG[C/T]TTTTTTTTTTGCCTG | 64326 |
rs77827395 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | RFWD2 | GRCh38.p7 | 1:175950042 | TTAAAATATGTACAA[C/T]TACCACTCTAAACCC | 64326 |
rs77845472 | snp | C/G | 0.0448719 | 0.142907 | intron-variant | RFWD2 | GRCh38.p7 | 1:176009056 | CTGCAGTTTTTCCTG[C/G]ATATGCACACTACAC | 64326 |
rs77845902 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176130008 | CCTATTCAATTACAC[A/G]TAATAATAAACTAAA | 64326 |
rs77869095 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176098662 | TAATCTGCTCTTTAG[C/G]AAAATTTGTAAAGGG | 64326 |
rs77874973 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175965050 | GCCTTAAGCTCTTTT[C/T]CATACCAAGATTATA | 64326 |
rs77879395 | snp | C/T | 0.0941369 | 0.195465 | intron-variant | RFWD2 | GRCh38.p7 | 1:176159972 | TATTATTTTCTGTAC[C/T]TTTCTGTATGCTGGA | 64326 |
rs77883966 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | RFWD2 | GRCh38.p7 | 1:176094173 | GTTTTGTTTTACTTA[C/T]TTGGCTTCCAGTTTT | 64326 |
rs77903848 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | RFWD2 | GRCh38.p7 | 1:176052936 | TTGCACAGATTTACA[C/T]TGCCTGGATGTATCA | 64326 |
rs77919346 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176183168 | CACCTATCACTAAAG[A/C]ATCATGCTCCAGATG | 64326 |
rs77928756 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | RFWD2 | GRCh38.p7 | 1:176090212 | TCCCTGTTCCCACCC[C/G]CTGTCCCTGCCTGCT | 64326 |
rs77947052 | snp | C/T | 0.0581099 | 0.160244 | intron-variant | RFWD2 | GRCh38.p7 | 1:176045908 | TAGAGTCTCCAACAA[C/T]CATGTCCAACAAAGA | 64326 |
rs77977242 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176186366 | AATTAAAAAAAAAAA[A/C]ACAAAAACTAGCAAG | 64326 |
rs77987810 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:176191928 | GCAATCATTTTAGAC[A/T]GTAATTTAACAATAA | 64326 |
rs77992782 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:176182347 | ACCAGAAGTAGAATC[C/G]TGGTCTAACAATATC | 64326 |
rs77997584 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176119781 | CAGTAACAATATCAA[C/T]AGTACCATTTACTGA | 64326 |
rs78005864 | snp | C/G | 0.0271762 | 0.113356 | intron-variant | RFWD2 | GRCh38.p7 | 1:176123187 | TCTGAAATAACCTCA[C/G]AAGTACTCCAGAAAT | 64326 |
rs78081681 | snp | C/T | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176059885 | CCTTTGTATTTTTTT[C/T]CAACCTTTGCAAATG | 64326 |
rs78118911 | snp | A/C/T | 0.00789609 | 0.0623361 | intron-variant | RFWD2 | GRCh38.p7 | 1:176184619 | GATTATTTTACTCAA[A/C/T]AGAATTGTCTTACCA | 64326 |
rs78122558 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | RFWD2 | GRCh38.p7 | 1:176117117 | TGGACAATTAACTTA[C/T]AATCAATTACTCAAG | 64326 |
rs78129579 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176182569 | GAATTATCTGGTCTA[A/G]TATGTCAATAGTGAC | 64326 |
rs78244947 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:176112467 | GCATATCTGTGGGGG[A/G]TACATGTAATATTTT | 64326 |
rs78258869 | snp | A/C | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176136575 | TAGAGAGAGAAAGAC[A/C]AAAAAAAAAAAGCCT | 64326 |
rs78275727 | snp | A/G | 0.363359 | 0.222822 | intron-variant | RFWD2 | GRCh38.p7 | 1:176058064 | CTCCGCCCGGCAGCC[A/G]CCCCGGCCGGGAGGG | 64326 |
rs78315735 | snp | A/C | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176091362 | AAAAAAAAAAAACAA[A/C]AAAAAAAACTTCTGA | 64326 |
rs78337215 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | RFWD2 | GRCh38.p7 | 1:176132352 | AAAACAGAATCCTCT[C/T]GCAAAGCCCTACCAT | 64326 |
rs78353537 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176149783 | AAAATTCACAAGAAC[A/C]AGGAATTCCAGGTTA | 64326 |
rs78354875 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | RFWD2 | GRCh38.p7 | 1:176079467 | GGAACAACACATACC[A/G]GGGACAACTAGATGG | 64326 |
rs78401348 | snp | C/T | 0.0689305 | 0.172377 | intron-variant | RFWD2 | GRCh38.p7 | 1:175965962 | CTAGACATAAATCTA[C/T]GCTGCATTTTGAAAC | 64326 |
rs78411325 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176065168 | AGCCTTACTTACTGT[C/G]TTTCAGTCAGATGAG | 64326 |
rs78420545 | snp | A/G | 0.0741063 | 0.177655 | intron-variant | RFWD2 | GRCh38.p7 | 1:176159443 | CACAAATCCACAGAA[A/G]AGCAATCTGTCAATA | 64326 |
rs78424263 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175951884 | AATATATGAAAACGT[A/T]AAGACTAAAATGTTT | 64326 |
rs78439371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175970499 | GTAATAGTTTAGATA[C/T]GATAGTCTAAGTGCA | 64326 |
rs78442081 | snp | G/T | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176041366 | TTCTTTTTTTTTTTT[G/T]AGACAGAGTCTCGCT | 64326 |
rs78442869 | snp | A/C | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176100411 | AAAAAAAAAAAAAAG[A/C]CTGGAGAGAGATAAA | 64326 |
rs78444217 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | RFWD2 | GRCh38.p7 | 1:175953660 | CACGCAAACATTAAT[C/T]GTAAGAAAGCTGGAA | 64326 |
rs78450381 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176099278 | CAATACAGGAAAAAC[A/G]TGCAGGACTCATGAA | 64326 |
rs78475696 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | RFWD2 | GRCh38.p7 | 1:176111727 | GTTCATACTTTTGGG[C/T]TTTTTTCAGTTTTAC | 64326 |
rs78482766 | snp | A/T | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:175989232 | AAGATTAAAAAAAAA[A/T]TCTACTATTTAAGAA | 64326 |
rs78507371 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | RFWD2 | GRCh38.p7 | 1:175950356 | TTACAAAAAAAGTTA[C/T]TTAGAATTAAACTAT | 64326 |
rs78512512 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | RFWD2 | GRCh38.p7 | 1:176121753 | CAATACTAAACTCTT[C/T]TCATGGTATCTGAAT | 64326 |
rs78541901 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | RFWD2 | GRCh38.p7 | 1:176105323 | ATAGAAGTAAATGAA[C/T]CTAACTGTATTTCAA | 64326 |
rs78569232 | snp | C/T | 0.0930568 | 0.194599 | intron-variant | RFWD2 | GRCh38.p7 | 1:176134846 | TGGCATGAAATCCAA[C/T]GCATTAAGGAAACAG | 64326 |
rs78574243 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:176200075 | ACCACCATTATTAAC[C/T]GTGTAACTGAGACAA | 64326 |
rs78661762 | snp | C/T | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992924 | CTGGAGATCTGAGAA[C/T]GGGCAGACTGCCTCC | 64326 |
rs78700901 | snp | A/G | 0.093417 | 0.194889 | intron-variant | RFWD2 | GRCh38.p7 | 1:175964559 | CAGAAACTGCAGCTG[A/G]GATGGCTAGCAAAGT | 64326 |
rs78720232 | snp | A/C | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176025461 | TGTCTACATTTAGCA[A/C]AAAAAAAAAAAACCT | 64326 |
rs78749109 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176096289 | TTTTCAGGACAGTAA[C/T]AGCACCTATCTTTTC | 64326 |
rs78823553 | snp | C/T | 0.093777 | 0.195178 | intron-variant | RFWD2 | GRCh38.p7 | 1:176029960 | TATTATTAGTAGTAG[C/T]ATTTTTTGAGACAAG | 64326 |
rs78824562 | snp | A/T | 0.093777 | 0.195178 | intron-variant | RFWD2 | GRCh38.p7 | 1:176045613 | AAGCAGATTCTAGAA[A/T]TCTTCTGAGATTTTT | 64326 |
rs78845402 | snp | A/G | 0.084364 | 0.187256 | intron-variant | RFWD2 | GRCh38.p7 | 1:176067813 | CCAAAACAGCATTCT[A/G]TAACACATGCCCACT | 64326 |
rs78847486 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:176085010 | CTACTTCATAGATGA[C/G]CAAAGACACTGAGAA | 64326 |
rs78894185 | snp | C/T | 0.0718919 | 0.175435 | intron-variant | RFWD2 | GRCh38.p7 | 1:175973501 | CAAGTTGCTAAATGT[C/T]ACACATTTTAAAGTA | 64326 |
rs78897181 | snp | C/T | 4.95013e-05 | 0.00497475 | intron-variant | RFWD2 | GRCh38.p7 | 1:176081130 | TCTTACAAAAGAAAA[C/T]AGTAATTTGACCAAT | 64326 |
rs78965446 | snp | A/G | 0.402806 | 0.197864 | intron-variant | RFWD2 | GRCh38.p7 | 1:176004899 | attccctctttttct[A/G]ttgattggaatagtt | 64326 |
rs78969508 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | RFWD2 | GRCh38.p7 | 1:176141138 | TAATTTTGAATACAT[C/T]ACATATAATTGTTCC | 64326 |
rs78984037 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176193476 | TACACAAATGTTCAC[A/G]GGAACATTATTCATA | 64326 |
rs78986327 | in-del | -/GTTA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176029256 | TTCTAGAATTATTTA[-/GTTA]AATTGCAAAATTTTG | 64326 |
rs78999728 | snp | A/C | 0.0391387 | 0.134304 | intron-variant | RFWD2 | GRCh38.p7 | 1:176161680 | TTAGTTCACAAACAC[A/C]CACATACAGCAGAAC | 64326 |
rs79018789 | in-del | -/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176016732 | TTTTATGAATGACTC[-/T]TTTTTTTAAAAAAAA | 64326 |
rs79046857 | snp | C/T | 0.0901694 | 0.192235 | intron-variant | RFWD2 | GRCh38.p7 | 1:176069638 | CATCCCCAGAGGGTT[C/T]TCCCTCACTTACTTA | 64326 |
rs79048236 | snp | C/T | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176038336 | AAATTGATCTATAGA[C/T]TGAATACAATGGCAA | 64326 |
rs79049458 | in-del | -/CTCT | 0.406814 | 0.194704 | intron-variant | RFWD2 | GRCh38.p7 | 1:176174089 | CATACTCATATATAA[-/CTCT]CTCTCACTATTTAGA | 64326 |
rs79061072 | snp | G/T | 0.0448719 | 0.142907 | intron-variant | RFWD2 | GRCh38.p7 | 1:176195093 | CCCTGTCTCAAAGAA[G/T]AGAAGAGAAAAAGGA | 64326 |
rs79065544 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:176154121 | AGAATACTTAGGGAG[G/T]AGTGCCTCTTCCTCA | 64326 |
rs79066726 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | RFWD2 | GRCh38.p7 | 1:176169623 | TTAAAAAATACTTTA[C/T]TGCTAAAAAATGCTA | 64326 |
rs79129926 | snp | A/G | 0.146985 | 0.227789 | intron-variant | RFWD2 | GRCh38.p7 | 1:176143379 | AACTTAAAACTTCCC[A/G]CAAACAATCACAGGT | 64326 |
rs79136116 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:175999235 | GTAGCCATTAACCAC[C/G]TCTACTTCCCCCAAC | 64326 |
rs79160076 | snp | C/T | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:175980684 | CCTAATGACCACTGC[C/T]TTTTTTTTTGCCTGA | 64326 |
rs79178486 | in-del | -/ACATC | 0.408359 | 0.193449 | intron-variant | RFWD2 | GRCh38.p7 | 1:176076547 | CAAATTAATGACCTT[-/ACATC]ACATGTAGAGGAACT | 64326 |
rs79225739 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176086517 | AGGCATGAGCCACTG[C/T]GCCTGGCCTGATTTT | 64326 |
rs79226426 | in-del | -/TG | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176173323 | CTCAAAAAAACAAAA[-/TG]AAAAAAAAAAAAAAA | 64326 |
rs79244242 | in-del | -/AA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176039591 | TACAGAAAAAAAAAA[-/AA]TTACCTTAAAATTCA | 64326 |
rs79259986 | snp | A/G | 0.021333 | 0.101051 | intron-variant | RFWD2 | GRCh38.p7 | 1:176095161 | CAATAAGTAAACTTT[A/G]TAAGTTCAAGGAATA | 64326 |
rs79266682 | snp | A/G | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176025904 | AAAAACCAAAAAAAA[A/G]GAAAACCCAAACAAA | 64326 |
rs79319944 | snp | C/T | 0.0941369 | 0.195465 | intron-variant | RFWD2 | GRCh38.p7 | 1:176058899 | TGGACTTCAAACATA[C/T]ATAAACCTAAGAGCT | 64326 |
rs79339960 | in-del | -/TT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176164848 | AAACTGATTTTTTTT[-/TT]AAAAAGGGAAACTAC | 64326 |
rs79355946 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175962092 | AAAGTCAGTGACTGC[C/T]TTTATGCAAAAAATA | 64326 |
rs79356337 | snp | G/T | | | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176208572 | TTATTTGGGAATAAA[G/T]TGTGAAAATACTCAT | 64326 |
rs79381546 | snp | G/T | 0.0314385 | 0.121371 | intron-variant | RFWD2 | GRCh38.p7 | 1:176112048 | TTCTTCCATAAGTAT[G/T]TTCTCTTTTAATCAT | 64326 |
rs79386048 | snp | C/T | 0.0894459 | 0.191631 | intron-variant | RFWD2 | GRCh38.p7 | 1:176181262 | TTTAGTGGTAATAAT[C/T]TGGATGAGCTTTGAA | 64326 |
rs79391253 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | RFWD2 | GRCh38.p7 | 1:176200417 | AGAGCCAAATGCCCA[C/T]CTGTGAATTAATACT | 64326 |
rs79392102 | snp | A/C | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176142717 | AACAGAAATCCAGAA[A/C]AAAAAAAAAACAAAA | 64326 |
rs79393117 | snp | C/T | 0.0689305 | 0.172377 | intron-variant | RFWD2 | GRCh38.p7 | 1:175980669 | ACAGAAAATGTCCAC[C/T]CTAATGACCACTGCT | 64326 |
rs79401439 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | RFWD2 | GRCh38.p7 | 1:176186957 | ACAGCTCCATCATCC[A/G]TTAGTTTATTTAAAA | 64326 |
rs79421526 | snp | A/C | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176091347 | CGAGACTCCGTCTCA[A/C]AAAAAAAAAAACAAA | 64326 |
rs79433644 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | RFWD2 | GRCh38.p7 | 1:176114068 | TAGCCTTGTCTGATG[C/T]TGATGTTCTGTGAAA | 64326 |
rs79439360 | snp | A/T | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176070366 | AACTTTTTTTTTTAA[A/T]TTAAAAACTCTGCCA | 64326 |
rs79452454 | snp | G/T | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176177200 | TTGCTAGAGAACTGT[G/T]ATTACAGAAAATTTT | 64326 |
rs79478013 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176076750 | CAAAGGAAAAAAAAA[-/A]GATTCAAATAAGCAC | 64326 |
rs79480972 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176074792 | TGGCTTTCAGGAATG[-/A]AAAAAAAAAAAAAAG | 64326 |
rs79522613 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176040751 | ATAGACTGTGCTCCA[C/T]TATTTCATTTCTTTT | 64326 |
rs79545531 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175965946 | GTTTCTTTACTTTAT[C/T]CTAGACATAAATCTA | 64326 |
rs79559632 | snp | A/T | 0.188631 | 0.242351 | intron-variant | RFWD2 | GRCh38.p7 | 1:176036287 | ACCCAAAGCAAGAAG[A/T]AAAATGGGCAGAAAT | 64326 |
rs79567575 | snp | A/G | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176045583 | GCTTGTTTAGAAGGA[A/G]AAAAAAAAAAAAAAA | 64326 |
rs79580490 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176049891 | AAAAGTTAAACAGTG[A/C]CTAGTTAGGCTGAGA | 64326 |
rs79636111 | snp | A/T | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176174570 | CTTCATAAAAAAAAA[A/T]TTACAGTGAAGAGTA | 64326 |
rs79656503 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176101208 | GGGTGGCACCCTATC[A/G]TGGCTGGTGGGACTC | 64326 |
rs79731276 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176197468 | GAATCTGCCTACACA[C/T]TGTTTTGTACTTCTA | 64326 |
rs79774945 | snp | A/G | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176174007 | AAAAAAAAAAAAAAA[A/G]AGAGAATATATATAA | 64326 |
rs79806301 | snp | C/G | 0.0532157 | 0.154195 | intron-variant | RFWD2 | GRCh38.p7 | 1:176001239 | ATTAACATCAGAATT[C/G]TCTGAATCATCAGAA | 64326 |
rs79809121 | snp | A/C | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176100393 | GACTTTGTCTCAAAA[A/C]AAAAAAAAAAAAAAA | 64326 |
rs79891703 | in-del | -/AAA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176190541 | ATTTAAAAAAAAAAA[-/AAA]CAGTACAGAACAGAT | 64326 |
rs79897786 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | RFWD2 | GRCh38.p7 | 1:176171948 | TAAGTAACAAATCAC[C/T]ATGACATTTAGATTC | 64326 |
rs79908440 | snp | A/C | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176136574 | ATAGAGAGAGAAAGA[A/C]AAAAAAAAAAAAGCC | 64326 |
rs79912506 | snp | A/T | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176194937 | TTAAAAAAAAAAAAA[A/T]TCAACCAGATGTGGT | 64326 |
rs79923623 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176084861 | CAGACTTTTTTTTTT[C/T]CCCCTTGGTGGGGTT | 64326 |
rs79927435 | snp | C/T | 0.00716266 | 0.059414 | intron-variant, downstream-variant-500B, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175968253 | CCTATTTTCAAAACT[C/T]GTAAGATACCTCAAA | 64326 |
rs80000614 | snp | A/G | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:175977967 | ATGAAAATTTGGTAG[A/G]GATTACCAAAAGATA | 64326 |
rs80003117 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | RFWD2 | GRCh38.p7 | 1:176131327 | AGGCAGAAGCAGTAA[A/G]ATAGGATATGACAAT | 64326 |
rs80003603 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176109630 | CTTTTAAATTGGAAT[A/C]TAATTAAATTAGTAA | 64326 |
rs80009119 | snp | A/C | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176179862 | CACTATCTCTCAGAC[A/C]AAAAAAAAAAAAATG | 64326 |
rs80075272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176188187 | TATGGCATTTTGTTA[C/T]AGCAGCCTGCACAGA | 64326 |
rs80080200 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176117076 | GTTAACACACCCTGC[C/T]ATGCCATTAAAAAGC | 64326 |
rs80105875 | snp | G/T | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:175950228 | TTAAAAAAAAAAAAA[G/T]TCAACATACGAATTG | 64326 |
rs80111009 | snp | A/G | 0.0383715 | 0.133092 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175969504 | GAAGCTCAACAAACA[A/G]GTCTTGCTAAGTTGC | 64326 |
rs80137408 | snp | A/G | 0.39121 | 0.2063 | intron-variant | RFWD2 | GRCh38.p7 | 1:176007259 | tctaaatttttttca[A/G]tgttttcaacttctt | 64326 |
rs80156138 | snp | C/G | 0.146985 | 0.227789 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176145905 | AAAAAGGGTGGTCAG[C/G]GTGCTTCAGCCGTTC | 64326 |
rs80163761 | snp | A/C | 0.0360663 | 0.129354 | intron-variant | RFWD2 | GRCh38.p7 | 1:176127023 | ATATAACCATGAGAA[A/C]AGGGTTCTAGGGTCT | 64326 |
rs80178461 | in-del | -/TG | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:176068423 | TGGAGCCCATCAATC[-/TG]TGTTTCAACAAGATC | 64326 |
rs80179612 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176170649 | GCAGAGCACAGACAC[A/G]GTAGATTTAGCATAA | 64326 |
rs80191494 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175970385 | GGGAATAGTATGGGA[A/C]AATGAAGAAACTTTC | 64326 |
rs80224650 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176041360 | CTTTTTTTCTTTTTT[C/T]TTTTTGAGACAGAGT | 64326 |
rs80228080 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176186365 | AAATTAAAAAAAAAA[A/C]CACAAAAACTAGCAA | 64326 |
rs80236800 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | RFWD2 | GRCh38.p7 | 1:176099867 | TTGAGACGTTAAGAG[A/G]GCAGGATCACCCAAC | 64326 |
rs80260662 | snp | C/G | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176051084 | AATAAGGTAGCCTCA[C/G]CGGTTTTATAATTAG | 64326 |
rs80262161 | snp | A/C | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176122139 | AGCAAGACTGCATCT[A/C]AAAAAAAAAAAAAAA | 64326 |
rs80290633 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | RFWD2 | GRCh38.p7 | 1:176198301 | ACATATATACACCAA[C/T]GGGACAGAATAAAAA | 64326 |
rs80301588 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:175972339 | AGGGAAAACCAAGAC[A/G]TATTTTTCTGCTTTT | 64326 |
rs111257958 | snp | A/G | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176103957 | ATGAAAAAACAAACA[A/G]GAAGAAATATTCTCT | 64326 |
rs111290429 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | RFWD2 | GRCh38.p7 | 1:176042574 | TCTCAAAAAAAAAAA[A/C]AAAAAAACTAGCCAA | 64326 |
rs111293336 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175993285 | TAGATAAAACCACAA[A/T]GATGGGGAAAAAACA | 64326 |
rs111295553 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175986646 | CAGAATGCATATTTT[A/G]GAGGAATTTCCAGTC | 64326 |
rs111302868 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175989198 | ATACAGACCAGAAAC[C/T]ACACTACTTTAATTG | 64326 |
rs111312096 | snp | C/T | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176045662 | TAGAGTCTTAACATA[C/T]TGTTAGTGTTTAAGA | 64326 |
rs111352725 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:176081079 | TTTAATAATAATGGT[A/G]TAAGTGCTTCTCAAA | 64326 |
rs111355551 | snp | C/G | 0.196771 | 0.244268 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992588 | AATGGCGGACCAGGA[C/G]ATTATATCCCGCACC | 64326 |
rs111358951 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176043118 | TATTTGTATTTCTGC[C/T]GATGAAAGGAATTAC | 64326 |
rs111419314 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175965584 | TTTTTTTTTGTTTTG[G/T]TTTTGTTTGTTTGTT | 64326 |
rs111431242 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175991695 | CCTTTTTACATTTCC[C/T]TATAAGTTAAAAAAT | 64326 |
rs111466447 | in-del | -/A | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176012008 | CTCCTTCTATTAATT[-/A]AAAAAAAAAACTGTA | 64326 |
rs111473562 | snp | A/C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176053471 | AAAATTATTCCTTGC[A/C/T]TAATTGTTAATTATT | 64326 |
rs111474996 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | RFWD2 | GRCh38.p7 | 1:176083735 | TTTACAGATTCTCAT[C/T]TGAAAATATACAAAG | 64326 |
rs111487842 | snp | C/T | 0.0543475 | 0.155628 | intron-variant | RFWD2 | GRCh38.p7 | 1:175991990 | AATAATGGTAAAAAG[C/T]AAATAATAAACAAGT | 64326 |
rs111489352 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RFWD2 | GRCh38.p7 | 1:176034029 | TGAGACTTTTACTGC[C/T]AAGCTGAGAGAGTAA | 64326 |
rs111490456 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | RFWD2 | GRCh38.p7 | 1:176198448 | CTTACCAAACACAGT[A/G]TATAAAAACTAACTT | 64326 |
rs111491780 | snp | A/C | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176169252 | TGGGGAGAAGGATAC[A/C]ACACACCTTGGTAAA | 64326 |
rs111517305 | in-del | -/ACACAC | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:175966281 | AATTGTGTTTGCAAT[-/ACACAC]ACACACACACACACA | 64326 |
rs111531372 | snp | C/T | 0.00164289 | 0.0286138 | synonymous-codon | RFWD2 | GRCh38.p7 | 1:175989442 | TACCATGATTGGCTG[C/T]TTAGTGTTACGAAGA | 64326 |
rs111531764 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176163221 | AAATATAAAAGGTGC[A/C]TTTGAGACTATTCTA | 64326 |
rs111550688 | snp | C/G | 0.0410537 | 0.137264 | intron-variant | RFWD2 | GRCh38.p7 | 1:176083712 | AAATAAAAGAGAATA[C/G]AGATGGATTTACAGA | 64326 |
rs111579173 | snp | C/T | 0.021333 | 0.101051 | intron-variant | RFWD2 | GRCh38.p7 | 1:176173572 | CTGAACCAGGGAGAT[C/T]AAGGCTGCAGTGAGC | 64326 |
rs111615547 | snp | C/G | 0.0352966 | 0.128072 | intron-variant | RFWD2 | GRCh38.p7 | 1:176154595 | CGATGAGGACACATG[C/G]ACACATAGAGGGGAA | 64326 |
rs111625933 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176086124 | AAATAAGCTCTAAAG[C/G]ACAGTTTTACAAGAC | 64326 |
rs111628004 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175947669 | GCCACTGTGCCCAGT[C/T]GAAGAGACAATTTTA | 64326 |
rs111648695 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176184991 | TTTAGTAGTACAATG[C/T]AGTCACCAGAGCCCT | 64326 |
rs111671442 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | RFWD2 | GRCh38.p7 | 1:176160005 | GATTCAGGTTAAATA[A/G]TAATGAAAAGTAAAA | 64326 |
rs111702930 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176176083 | CACAAAATAATGACT[A/G]TTAGTCTTCTATTCC | 64326 |
rs111710743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176050124 | ATACTTTTGAAAAAT[C/T]GTGTTTCTGGGGACA | 64326 |
rs111724138 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | RFWD2 | GRCh38.p7 | 1:176052803 | TTTTCAATTAAACAT[A/T]TGAGATGACATCATA | 64326 |
rs111728322 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | RFWD2 | GRCh38.p7 | 1:176139120 | AAAATGGGCACAGAC[A/G]TAAACAGACAATTCC | 64326 |
rs111732929 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:175952588 | TTCAGGATGAAGGAA[G/T]ATTATACTACATGAA | 64326 |
rs111734323 | in-del | -/AGTT | 0.0130921 | 0.0798413 | intron-variant | RFWD2 | GRCh38.p7 | 1:176083703 | ATAGTTGGAAATAAA[-/AGTT]AGAGAATACAGATGG | 64326 |
rs111788931 | snp | A/T | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:175975272 | ATCCCCCACCCCAAA[A/T]CCTTCCCCACTCCCA | 64326 |
rs111801798 | snp | A/C | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176175547 | CTGAGAATCTAATGC[A/C]ACCCACTGATCTGAC | 64326 |
rs111810444 | snp | A/G/T | 0.00199529 | 0.0315338 | intron-variant | RFWD2 | GRCh38.p7 | 1:176032407 | CAGACCATGTATTAG[A/G/T]AGCTAGACGTTGTCA | 64326 |
rs111822734 | in-del | -/A | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176002603 | TGAGTGAGAATATGC[-/A]GTGTTTGGTTTTTTG | 64326 |
rs111827393 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176135259 | AAGCAAGGACATGTG[A/T]AAAGTTAAGAGACAA | 64326 |
rs111831637 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | RFWD2 | GRCh38.p7 | 1:175996301 | ATATCATACTGAATG[A/G]GCAAAAACTGGAAGC | 64326 |
rs111836936 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175996261 | CTCAAAATAATAAGA[A/G]CTATCTATGACCAAC | 64326 |
rs111852306 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176106570 | AGCTGGCAACACCCA[C/G]ATTGATTAACTGGCC | 64326 |
rs111859434 | snp | C/G | 0.198634 | 0.244666 | intron-variant | RFWD2 | GRCh38.p7 | 1:176049027 | AATACAAAAAATTAG[C/G]CAGGCGCGGTGGCGG | 64326 |
rs111885828 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176023734 | AAAAAAAAAAAAAAA[A/G]AAAAAGAAAAGAAAA | 64326 |
rs111901403 | snp | A/G | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176188886 | AAGCATCCCAGAGTT[A/G]TGACATATGTGAAAT | 64326 |
rs111932114 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | RFWD2 | GRCh38.p7 | 1:176026699 | AAAGTATAGTGACAT[A/G]GTTTAAATTATGCAT | 64326 |
rs111932433 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176046753 | TTCACAATATTAAAT[G/T]TTATTTTTAATAAAT | 64326 |
rs111948105 | snp | A/C | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176126774 | TCACTTTTTAAGTAT[A/C]AACTGAAATGATGAT | 64326 |
rs111984554 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176042910 | GGCACGTGGCTGTAA[C/T]TCCAGCTACTCGGGA | 64326 |
rs111986212 | snp | A/G | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176136233 | ACTCCAAGAAAACTG[A/G]GCGATTTTTTTTGTC | 64326 |
rs112023767 | snp | A/T | 0.040671 | 0.13668 | intron-variant | RFWD2 | GRCh38.p7 | 1:175999487 | TTTTGTATATGTACC[A/T]CATTTCCCTTATTCA | 64326 |
rs112044655 | snp | G/T | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176022981 | TGTTACAAGCACCAT[G/T]GTAGAGATGTGGGGG | 64326 |
rs112097869 | snp | C/T | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:175981515 | ACACCATATACAACA[C/T]TCAACTCAAAATGAT | 64326 |
rs112134749 | in-del | -/AAAAT | 0.116488 | 0.211364 | intron-variant | RFWD2 | GRCh38.p7 | 1:176077913 | ACAATAGCCACAAAG[-/AAAAT]GAAAATAACTAGGAA | 64326 |
rs112136586 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176064132 | ATGGGTCAAATTTGG[C/T]CCATGGTCCATAGTT | 64326 |
rs112140281 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176049188 | CGTCTCAAAAAAAAA[A/G]AAAAAAAAAAAAAAA | 64326 |
rs112154296 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | RFWD2 | GRCh38.p7 | 1:176071257 | CCCCTCCTTTAGCTA[C/T]GTGACTTGCCTGCTC | 64326 |
rs112172228 | snp | A/G | 0.389903 | 0.207189 | intron-variant | RFWD2 | GRCh38.p7 | 1:176057997 | ccgccccgtctgaga[A/G]gtgaggagcccctcc | 64326 |
rs112186374 | in-del | -/C | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176179652 | GAAGCAGGAGGATTG[-/C]CTTGAGCCCAGGAGA | 64326 |
rs112243330 | snp | A/G | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176013960 | AATCATTGATTAAGA[A/G]TTCATTCCAATAAGT | 64326 |
rs112275537 | snp | C/G | 0.0387552 | 0.1337 | intron-variant | RFWD2 | GRCh38.p7 | 1:176044239 | CAAATAAACTACAGT[C/G]AATTGGGTTTCTGTA | 64326 |
rs112300770 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176184926 | GAGCTTCAAAATGAA[C/G]TCAATGAGTAAATCA | 64326 |
rs112307589 | snp | C/T | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176125913 | TTCATCAGTGCTTTA[C/T]AGTTTTCATTATAGA | 64326 |
rs112318287 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176179290 | GTGAGACTCCGTCTC[A/C]AAAAAAAAAAAAATT | 64326 |
rs112343441 | snp | C/T | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176153002 | AAATAAGGGTACAGA[C/T]ATACCTGAGAATGCA | 64326 |
rs112381794 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | RFWD2 | GRCh38.p7 | 1:176077233 | ATCCTCGACAAAATA[C/T]TCTGTATTTGTTCAG | 64326 |
rs112387124 | snp | A/C | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176040944 | TAACATAGCTTTATA[A/C]ACTTAATGGTGAGAA | 64326 |
rs112419672 | snp | C/T | 0.0894459 | 0.191631 | intron-variant | RFWD2 | GRCh38.p7 | 1:175983313 | GGGGCAAGTCTTTCC[C/T]GAACTGTTCTCGTGA | 64326 |
rs112425301 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176162815 | TTTCTACGTCTTTTT[C/T]ATTGCAATAAAGTTC | 64326 |
rs112434112 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176188740 | TAGATGGCAAACCTC[A/G]CTGTGTTCTTACTCC | 64326 |
rs112449726 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | RFWD2 | GRCh38.p7 | 1:176035804 | AGAACACTCACCAAA[C/G]AGCATTTATAGTACA | 64326 |
rs112511964 | snp | A/C | 0.040671 | 0.13668 | intron-variant | RFWD2 | GRCh38.p7 | 1:176149302 | GTTCTAAATTACATC[A/C]CTTATCTAACATGCT | 64326 |
rs112515395 | snp | C/T | 0.401924 | 0.198543 | intron-variant | RFWD2 | GRCh38.p7 | 1:175983646 | cagaggttggaacag[C/T]ttagagggttcagaa | 64326 |
rs112525302 | snp | A/G | 0.0596104 | 0.162024 | intron-variant | RFWD2 | GRCh38.p7 | 1:176093392 | TAAGATTGTAATTCT[A/G]GATTTTAGCCTACAG | 64326 |
rs112572570 | snp | A/G | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176159982 | TGTACTTTTCTGTAT[A/G]CTGGAAAGATTCAGG | 64326 |
rs112596804 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176046635 | AGAAAGATTTAATGG[C/T]GTGAATCATTTGATA | 64326 |
rs112632438 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175958377 | TCTGTAACCATTCAG[A/G]TATAATATCAAAGCC | 64326 |
rs112655295 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176042968 | CGGGAGGCAGAGGTT[A/G]CACTGAGCCACAATT | 64326 |
rs112668376 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | RFWD2 | GRCh38.p7 | 1:176141465 | GAGATAGTGCCACTG[C/T]ACTCCAGCCTGGGCA | 64326 |
rs112680443 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | RFWD2 | GRCh38.p7 | 1:176094947 | AAAGACTAATGAAAT[C/T]AATGCTTGTATAATA | 64326 |
rs112686970 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176008181 | CTTCCCAAGTGAGGC[A/C]ATGCCTCGCCCTGCA | 64326 |
rs112708530 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175997069 | TAGATCAATGGAACA[G/T]AACACAGTCCTCAGA | 64326 |
rs112735159 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176024042 | GCAGGCAGATCACTT[A/G]AGGTCAGGAGTTCGA | 64326 |
rs112767731 | snp | A/G | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176023740 | AAAAAAAAAAAAAAA[A/G]AAAAGAAAAGAAAAG | 64326 |
rs112782508 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | RFWD2 | GRCh38.p7 | 1:176195327 | AAGCTTCAAAATACA[C/T]GAAGCAAAAGCTGAG | 64326 |
rs112783494 | snp | A/G | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176129438 | CATGTCTGCATGACA[A/G]TTTTTTAAAAAAAAT | 64326 |
rs112825791 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176127567 | AGTATTCTACTGTGT[G/T]TGTGTGTGTGTGTGT | 64326 |
rs112827369 | snp | A/T | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:175989313 | ACAAGCTGGTAGGTA[A/T]GTACAGAGCTCTGTA | 64326 |
rs112830682 | snp | G/T | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:175993269 | CATCAAAGACCAAAA[G/T]TAGATAAAACCACAA | 64326 |
rs112847513 | snp | C/T | 0.040671 | 0.13668 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176186457 | GAGGAAGAATGATCA[C/T]TTGAGCACAGCAGGC | 64326 |
rs112861612 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175988087 | AGGTGTTCAGGGTTT[C/G]TACACAATAAAAAAG | 64326 |
rs112904877 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176077913 | TACAATAGCCACAAA[G/T]AAAATAACTAGGAAC | 64326 |
rs112913001 | snp | C/T | 0.0667028 | 0.170006 | intron-variant | RFWD2 | GRCh38.p7 | 1:176019505 | TAATAATAATAATAA[C/T]AACCATCATCATCAT | 64326 |
rs112939827 | snp | A/C | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:175993257 | GTATATCACCACCAT[A/C]AAAGACCAAAAGTAG | 64326 |
rs112960896 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176081622 | GGAGAATGTGAGGAT[A/G]TTAAGAAGAGTACTG | 64326 |
rs112966719 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:176020064 | GGCATGGTGGCTCAC[A/G]TCTATAATCCCAGCA | 64326 |
rs112970168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176023500 | GAGGCGGGTGGATCA[C/T]CTGAGGTCAGGAGTT | 64326 |
rs112974214 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176148645 | ACATATGTTTTTACC[A/G]TAAGAAAAAAACTAT | 64326 |
rs112982009 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176090852 | GAGTTGATGGCTGAG[A/G]TTTTTCCAGAACTGA | 64326 |
rs112992766 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176175672 | AGTCCATGGCCCAGG[A/G]GTCCCTGATATACAC | 64326 |
rs112993608 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | RFWD2 | GRCh38.p7 | 1:176117627 | AGGCTAGGCACGGTC[A/G]CTCACGCCTGTAATC | 64326 |
rs113026512 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176199416 | TGGCAGAGAACTCAG[A/C]AATTCACTACTAGAT | 64326 |
rs113042603 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176185053 | CATGTACTCAAAAGC[A/G]TGTACCGAGACCTGC | 64326 |
rs113046806 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | RFWD2 | GRCh38.p7 | 1:176156090 | AGCCAAAATAACAAT[A/G]TTTTAAAAAAGAAAA | 64326 |
rs113092233 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176178352 | ACAAAAAAAAAAAAA[C/T]AATAATAATAAATGC | 64326 |
rs113097981 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176174653 | AACCATAGCTGAATA[C/T]GTTCAAATTCATAAT | 64326 |
rs113111362 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | RFWD2 | GRCh38.p7 | 1:176064903 | CTTAGGATTTTAAGC[A/G]TGAGCCACCATGCCT | 64326 |
rs113138284 | snp | A/C | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176079218 | AGCTATTCACAGTAA[A/C]GAAGACATGTAATCA | 64326 |
rs113139552 | snp | C/T | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176100127 | GGGTGCGGTGGCTCA[C/T]GCCTGTAATCCTAGC | 64326 |
rs113140584 | snp | C/T | 0.0349115 | 0.127424 | intron-variant, downstream-variant-500B, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175968165 | GTGAGCCACCATGCT[C/T]GGCAAGAGAAGAATA | 64326 |
rs113196459 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176006878 | TTCTCTGTATTTCCT[C/G]AATCTGAACGTTGGC | 64326 |
rs113197099 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176043544 | ATATGGTACCAAAAG[A/T]GGGAGACAGGAAAAA | 64326 |
rs113208109 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176185778 | CTCCGCTGGACTTCA[C/T]ATTACATGAGAAGGT | 64326 |
rs113228008 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175944831 | CTTTCCAAGCTCAAC[C/T]GTGGCTCAATAAACT | 64326 |
rs113270766 | snp | A/G | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176139275 | AAAAGTGAAAAAACA[A/G]AAACAAAAAAAACAA | 64326 |
rs113303187 | in-del | -/T | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176141735 | GCACTTTTTCTTTTC[-/T]TTTTTTTTTTTTTAA | 64326 |
rs113315470 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | RFWD2 | GRCh38.p7 | 1:176115672 | GAGAATCACTTGAAC[C/T]CAGGAGGAGGTTGCA | 64326 |
rs113348451 | snp | A/G | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176070604 | AAGGCAGAGGTTGCA[A/G]TGAGCCAAGACCGCA | 64326 |
rs113349669 | snp | C/T | 0.0603597 | 0.1629 | intron-variant | RFWD2 | GRCh38.p7 | 1:175990633 | TTAAATATCACAGAT[C/T]TTCTTTTCATATATC | 64326 |
rs113361536 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175989029 | CATTCTATTGCATCA[A/C]CTATGTTGTTTATCT | 64326 |
rs113364157 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175995952 | ACAACCAAAAAAGAG[A/G]ATTTTAGACCAATAT | 64326 |
rs113369765 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175996725 | CAAGGAGAACTACAA[A/C]CCACTGCTCAGTGAA | 64326 |
rs113371470 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | RFWD2 | GRCh38.p7 | 1:175993021 | ACTGACACCTCACAC[C/T]GCCGGGTACTCCTCT | 64326 |
rs113374888 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | RFWD2 | GRCh38.p7 | 1:175977695 | TTCCCCAGACAATCT[A/G]TATATTCTTAAATTA | 64326 |
rs113388406 | snp | A/C | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176073683 | TCACCAATTCCGTAC[A/C]TTGTCTATTGTTTAA | 64326 |
rs113409376 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | RFWD2 | GRCh38.p7 | 1:176083182 | TCCTATTACTGTGAG[A/T]TATTTAACATTCTAC | 64326 |
rs113413256 | snp | A/T | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:175950723 | AATAAAATACCCAAT[A/T]TTTTTTTCTGACTAT | 64326 |
rs113420292 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176062774 | TACAATTATTCAAAT[A/G]AATAAACTGTAGAAT | 64326 |
rs113439238 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175965585 | TTTTTTTTGTTTTGT[G/T]TTTGTTTGTTTGTTT | 64326 |
rs113461876 | snp | A/G | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:175981544 | ATTAGAGGCTTAAAC[A/G]TAAGACTGAAAACTG | 64326 |
rs113475608 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | RFWD2 | GRCh38.p7 | 1:176183059 | CATTGCTGTTATCAT[C/T]TTAATACTTTATTTT | 64326 |
rs113508237 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176016739 | GAATGACTCTTTTTT[A/T]AAAAAAAAAAATTAC | 64326 |
rs113514457 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176163096 | CATTACATAGATATC[A/G]AAAATATATTATAAT | 64326 |
rs113521953 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175995951 | CACAACCAAAAAAGA[A/G]AATTTTAGACCAATA | 64326 |
rs113554223 | snp | C/T | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:175979136 | TGATTGTTCATATAA[C/T]TTCCCAAGGAGACCT | 64326 |
rs113566316 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | RFWD2 | GRCh38.p7 | 1:176064268 | AAATTGCCAAAAAAT[C/T]TGTCATATTTCATTT | 64326 |
rs113573986 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175987218 | ATCTTTTATGGGCAA[A/C]TTTGAAAGGCTAGAT | 64326 |
rs113594367 | snp | C/T | 0.00162402 | 0.0284495 | intron-variant | RFWD2 | GRCh38.p7 | 1:176043299 | GACAGTAGCCTCAGA[C/T]AGAATACAGATCTCA | 64326 |
rs113595802 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175965648 | GGCTGGACTGCAGTG[A/G]TGCAGTCTCGGCTCA | 64326 |
rs113607551 | in-del | -/TTTTTTC | 0.046775 | 0.145601 | intron-variant | RFWD2 | GRCh38.p7 | 1:176041346 | TTGGATTTTTTTTCT[-/TTTTTTC]TTTTTTCTTTTTTTT | 64326 |
rs113611827 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992137 | GGAATATGAGATGTT[C/T]TGATACAGGCATGCA | 64326 |
rs113633478 | snp | A/G | 0.0941369 | 0.195465 | intron-variant | RFWD2 | GRCh38.p7 | 1:176093656 | CATCCTGGCTAACAC[A/G]GTGAAACCCCGTCTC | 64326 |
rs113687730 | snp | C/T | 0.00318978 | 0.0398085 | downstream-variant-500B | RFWD2 | GRCh38.p7 | 1:175944702 | GTTTACATTGATATG[C/T]GTAATTCCCAAAGAG | 64326 |
rs113700633 | in-del | -/A | 0.0170251 | 0.090679 | intron-variant | RFWD2 | GRCh38.p7 | 1:176119403 | TGATATTGATATCTC[-/A]GTGTATACAGTGATA | 64326 |
rs113711725 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176176096 | CTATTAGTCTTCTAT[C/T]CCTCATTTTCAACAT | 64326 |
rs113796736 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:176165657 | TGTCACTGCACTGCA[A/G]CCTAGGAGATAGAGC | 64326 |
rs113825365 | in-del | -/A | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176088997 | CAAAACTCAGTCTCC[-/A]AAAAAAAAAAAAAAA | 64326 |
rs113846209 | snp | A/G | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176013335 | TTAGCTAGGGGGAAA[A/G]ACACAAGATGATGAT | 64326 |
rs113897469 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176136355 | AATTCATCCTCAATT[A/G]AAATGAAAGTAACAG | 64326 |
rs113901196 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176114067 | GTAGCCTTGTCTGAT[A/G]TTGATGTTCTGTGAA | 64326 |
rs113906866 | snp | C/G | 0.0352966 | 0.128072 | intron-variant | RFWD2 | GRCh38.p7 | 1:176143107 | TTCCTGGCAAGAATT[C/G]ATCCAACAGAACAAG | 64326 |
rs113960895 | snp | C/G | 0.447809 | 0.152878 | intron-variant | RFWD2 | GRCh38.p7 | 1:176057882 | cgccatcccatctag[C/G]aagtgaggagcgtct | 64326 |
rs113961673 | snp | A/G | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:175988651 | CAGCCTGGCCAACAT[A/G]GCAAAACACCGTCTC | 64326 |
rs114018622 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | RFWD2 | GRCh38.p7 | 1:175950202 | GCAGAAACAGATAAA[C/T]ACTTTATGTGTTAAA | 64326 |
rs114055994 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | RFWD2 | GRCh38.p7 | 1:176080688 | ACAAATGTCTTAAAA[C/G]ACACAAACTAATTAT | 64326 |
rs114057101 | snp | G/T | 0.0267878 | 0.112589 | intron-variant | RFWD2 | GRCh38.p7 | 1:176067010 | CTTATTGGGCAAGAA[G/T]CTCTAGAAACTAAAT | 64326 |
rs114068014 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176021888 | CTGATTGAAAACAAC[A/G]TGGATTTCTCTAGCT | 64326 |
rs114090236 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | RFWD2 | GRCh38.p7 | 1:176038064 | TCTGAAAAAGTAATC[C/T]ATACCTACAGTGACT | 64326 |
rs114127790 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | RFWD2 | GRCh38.p7 | 1:176189369 | TTCATTGTTTCTAGG[A/G]ACAGTATTATGTTTC | 64326 |
rs114144932 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176133239 | ACGTACGTATATGTA[C/G/T]GTAGGTACACACATA | 64326 |
rs114157787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176122868 | AAAATTTCTAAAAGA[C/T]GGAACAGGTCTGAGT | 64326 |
rs114179676 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | RFWD2 | GRCh38.p7 | 1:176192391 | CCAGGCCTCAAACAC[A/G]GACACAGATCTTCAC | 64326 |
rs114239127 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | RFWD2 | GRCh38.p7 | 1:176118431 | TTGACAGAAGATTAC[A/G]GTGACTATAGTTAAC | 64326 |
rs114247969 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:176170123 | ATTCTAGCTCTCTGG[C/T]TACTTCCTCCACATA | 64326 |
rs114259471 | snp | G/T | 0.021333 | 0.101051 | intron-variant | RFWD2 | GRCh38.p7 | 1:176201504 | GAACATATCCACCTA[G/T]GTAATGTTGGCTCAT | 64326 |
rs114259741 | snp | A/G | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175968613 | AACTAACTGCATCAA[A/G]TTCTCATTTAAATAT | 64326 |
rs114266163 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176090099 | TCTTAACCCAGACAC[A/T]CCTTCCTATTAATCT | 64326 |
rs114305700 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | RFWD2 | GRCh38.p7 | 1:175959695 | AAATATGTTTATTGG[C/T]TAACTTGAATAGATA | 64326 |
rs114307516 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | RFWD2 | GRCh38.p7 | 1:176204000 | AAGGGAGTGGTGAGG[A/G]ATAAAACATTTATCT | 64326 |
rs114319140 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:176183430 | CATCAGGATGGCTAC[C/T]ATCAAAAACCAACAA | 64326 |
rs114324718 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | RFWD2 | GRCh38.p7 | 1:176106269 | CTTCTGACCTCAGGT[A/G]GTCCATCCACCTTGA | 64326 |
rs114361611 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | RFWD2 | GRCh38.p7 | 1:176098192 | ATAAGGAACTAACCA[C/T]GCCCTTAATTATGCT | 64326 |
rs114362071 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | RFWD2 | GRCh38.p7 | 1:176157777 | AAGAAACAAGCATGC[A/G]AAGAAGCAGAAAAAT | 64326 |
rs114364964 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176124922 | CTCCACATCTTCACT[A/C]GCATTTGTTACTGCC | 64326 |
rs114367889 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | RFWD2 | GRCh38.p7 | 1:176057341 | TCTCCCTCTCCCCAC[A/G]GATTCCCTCTCCCTC | 64326 |
rs114376530 | snp | A/C | 0.021333 | 0.101051 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176185052 | ACATGTACTCAAAAG[A/C]GTGTACCGAGACCTG | 64326 |
rs114381107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176167751 | TGCTTGAGCCAAATT[A/G]CCTAAGACCAAATTC | 64326 |
rs114392239 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | RFWD2 | GRCh38.p7 | 1:176105327 | AAGTAAATGAACCTA[A/G]CTGTATTTCAAAGAA | 64326 |
rs114402112 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | RFWD2 | GRCh38.p7 | 1:176036871 | GACTTATTGGGACTG[C/T]AATCCCATTGTAAGT | 64326 |
rs114405700 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | RFWD2 | GRCh38.p7 | 1:176075477 | TTTTTAGGGTTATTC[A/G]TTCTAAGAGATTTGA | 64326 |
rs114408259 | snp | A/T | 0.0217236 | 0.101931 | intron-variant | RFWD2 | GRCh38.p7 | 1:176172684 | GAACTGCAGGCATTA[A/T]GCAAATCATGCCGTC | 64326 |
rs114409469 | snp | C/T | 0.0689305 | 0.172377 | intron-variant | RFWD2 | GRCh38.p7 | 1:175975642 | TTGAAATCCTAGCCT[C/T]AAGTGATCCACCCAC | 64326 |
rs114446684 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | RFWD2 | GRCh38.p7 | 1:176107774 | CAGCACTGAGACAAA[C/T]AGATACCATATGCCT | 64326 |
rs114464023 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | RFWD2 | GRCh38.p7 | 1:175999770 | CATCCTCACCAGCAT[C/T]TGTTTACTGCCTAAC | 64326 |
rs114479992 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176177621 | TCAGGAAAAAAATGA[G/T]TTCTAAGAAATTACA | 64326 |
rs114516818 | snp | A/C | 0.0225045 | 0.103662 | intron-variant | RFWD2 | GRCh38.p7 | 1:176140981 | GTAAGTCTCAGAATC[A/C]CTTACGAAGATAATA | 64326 |
rs114550102 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | RFWD2 | GRCh38.p7 | 1:176069565 | AACTATCCAGTGCTA[G/T]AAGTACAAAGATGAA | 64326 |
rs114560531 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | RFWD2 | GRCh38.p7 | 1:176032249 | CTATTTCAACAAAAA[C/T]TACCATAAAACTCAG | 64326 |
rs114585536 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | RFWD2 | GRCh38.p7 | 1:175946401 | TCCACTTATGATGAG[C/T]CTAAGGAAGCTATGG | 64326 |
rs114600364 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | RFWD2 | GRCh38.p7 | 1:176180921 | ATGCTGGGAGATGAC[A/G]ATGCTGAAGGACCCC | 64326 |
rs114608697 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | RFWD2 | GRCh38.p7 | 1:176029181 | AATTAAGAATTTCAT[G/T]ATTTTAAATTTTTAT | 64326 |
rs114613655 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176185605 | AAAAGACATTTCCTT[C/T]TATCCTTCCCTTTTC | 64326 |
rs114615159 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | RFWD2 | GRCh38.p7 | 1:176062358 | ATAGACAATTCACAA[A/T]AGATATACAAATAGT | 64326 |
rs114646139 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | RFWD2 | GRCh38.p7 | 1:175972129 | CATAACAACAACAAC[A/G]ACAACAACAAATACA | 64326 |
rs114673964 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | RFWD2 | GRCh38.p7 | 1:176105017 | TCCTCATAAATTGTT[A/G]AATAAAGTACAGAAA | 64326 |
rs114675289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176056788 | AGTATTTGACCATCT[A/G]ATTTCTTTCTTTTGT | 64326 |
rs114677160 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | RFWD2 | GRCh38.p7 | 1:176102599 | TTTACAGCTTAAAAA[A/C]CATGAAAACAGCCCT | 64326 |
rs114678535 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant | RFWD2 | GRCh38.p7 | 1:176014469 | TAATTATCTGTTAGA[A/C]GTCATTACCCTCAAA | 64326 |
rs114684796 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | RFWD2 | GRCh38.p7 | 1:176184190 | CTGGCATGATATAAT[A/G]TAAAGTTAATATTGA | 64326 |
rs114685224 | snp | C/T | 0.021333 | 0.101051 | intron-variant | RFWD2 | GRCh38.p7 | 1:175962586 | ACTATTCCAACCCAC[C/T]CCTGGCAGCTGATTC | 64326 |
rs114756098 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176087751 | TCAGCCACCCCATTA[C/T]GGGTTATATACCCAA | 64326 |
rs114780201 | snp | G/T | 0.0193772 | 0.0965046 | intron-variant | RFWD2 | GRCh38.p7 | 1:176139509 | CCCCAAAGACAAGTG[G/T]ATTTGTATGTTCATC | 64326 |
rs114808691 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | RFWD2 | GRCh38.p7 | 1:176114522 | ATATACAAATAAATG[C/T]TCATTAAAAACACCT | 64326 |
rs114811189 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:175991200 | GTGAGCATACAGTGT[A/G]CTTTCACAAACCTAG | 64326 |
rs114817238 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207722 | GTAGGCAGGTGCTTC[C/T]GAATCGCGGAATGTA | 64326 |
rs114823654 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | RFWD2 | GRCh38.p7 | 1:176022344 | CAAACTATAATTGGT[A/G]GGTAGCTCATATACT | 64326 |
rs114887560 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | RFWD2 | GRCh38.p7 | 1:176084028 | ACCTTTACTATTCCA[C/T]ACCATATCTATGCTG | 64326 |
rs114894069 | snp | A/C | 0.0217236 | 0.101931 | intron-variant | RFWD2 | GRCh38.p7 | 1:176023400 | CCAATAAATTAGAAA[A/C]CTTAGAAAATATGAA | 64326 |
rs114895702 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:176156126 | GTTTGGTGAGACTTA[C/T]AACATGGTTTGAACC | 64326 |
rs114925982 | snp | A/C | 0.0456336 | 0.143994 | intron-variant, downstream-variant-500B | RFWD2 | GRCh38.p7 | 1:175967456 | ATGCCACTGCACTCC[A/C]ACCTGGGTGACACAG | 64326 |
rs114928530 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | RFWD2 | GRCh38.p7 | 1:176143626 | AACCAAACCATATAG[A/G]AGAGAATATACATAA | 64326 |
rs114938765 | snp | C/G | 0.0217236 | 0.101931 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176176293 | GCAATTTAGATAGTT[C/G]ATAACAACACCAGAA | 64326 |
rs114966784 | snp | C/T | 0.0170251 | 0.090679 | intron-variant, downstream-variant-500B | RFWD2 | GRCh38.p7 | 1:175967308 | TGAGCCACCGCGCCG[C/T]TGAAAGCTCATCTCT | 64326 |
rs114977892 | snp | A/G | 0.021333 | 0.101051 | intron-variant | RFWD2 | GRCh38.p7 | 1:176051108 | TAATTAGTAGAAGAG[A/G]TTACAGACAATATAT | 64326 |
rs115027443 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | RFWD2 | GRCh38.p7 | 1:175980864 | ATAGGGTATCTGCAG[C/T]CTCAAAAGAAGTTAC | 64326 |
rs115058686 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | RFWD2 | GRCh38.p7 | 1:176142278 | ATTCCGAAAAGAAAC[C/T]GTTCAAAAACCCATG | 64326 |
rs115066674 | snp | A/G | 0.466824 | 0.124448 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176176821 | TGAAAAAAAGAGAAA[A/G]AAAAGACAAAAGAAA | 64326 |
rs115085997 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:176167389 | GTCCCTGACGCATAG[C/T]AGGCGCCTGGTATTT | 64326 |
rs115109206 | snp | C/G | 0.0209421 | 0.100162 | intron-variant | RFWD2 | GRCh38.p7 | 1:176197101 | TAAAGAAATAATCAA[C/G]GTAAAATACAGTCAT | 64326 |
rs115150424 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | RFWD2 | GRCh38.p7 | 1:176131239 | GAAAGAAACATCATA[C/T]TTCTGGCAATAACAC | 64326 |
rs115202800 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176026472 | GTTAAAGAACTTGCT[C/G]AAGGTCACATTTCTA | 64326 |
rs115282862 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176066900 | CCTTGGAACAGTTGG[G/T]TACCAGCTGTTTTCC | 64326 |
rs115287115 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | RFWD2 | GRCh38.p7 | 1:176098460 | TTAACAGAGCGAGAC[C/T]CCATCTCAAAAAACA | 64326 |
rs115315579 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:176123466 | TAATAATTAAAGGGG[A/T]AAAGAGTTTCCTATG | 64326 |
rs115328639 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176125018 | TTTCTGATGATCAAT[C/G]ATGTTGAACACTTCC | 64326 |
rs115357892 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176124750 | ATGCAGATAACTCTT[C/T]CATGTATACGTTTCC | 64326 |
rs115371339 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant | RFWD2 | GRCh38.p7 | 1:176163360 | TAAGCCTTTAAAATT[A/G]AGAATCTTTCAAAGG | 64326 |
rs115380656 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | RFWD2 | GRCh38.p7 | 1:176053290 | TGGAAGTAAATTCAG[C/T]GTGCTTACTATACAT | 64326 |
rs115399571 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207661 | ATGCGTGCGAACGCA[C/T]CACATTCCGGAACGG | 64326 |
rs115405484 | snp | A/T | 0.021333 | 0.101051 | intron-variant | RFWD2 | GRCh38.p7 | 1:176061641 | CAAAATAAAAAAAAG[A/T]AAAAGAAAAAGAAAA | 64326 |
rs115434945 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | RFWD2 | GRCh38.p7 | 1:176085379 | TGCTTTCCCTGACTC[A/G]ATTTACAACACTCCT | 64326 |
rs115466880 | snp | A/C | 0.33456 | 0.235265 | utr-variant-5-prime, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176206983 | CTACCAGACATCGTG[A/C]CTCCCTCCCCTCCAG | 64326 |
rs115481769 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176057210 | TACCTGCTATGTAGC[A/T]CCGAAATGATTCTAA | 64326 |
rs115512099 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | RFWD2 | GRCh38.p7 | 1:176104200 | TAAACTCCAAATAGA[C/T]TGAGAATTTAAATGT | 64326 |
rs115515068 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | RFWD2 | GRCh38.p7 | 1:176101679 | GGTCTCGAGATTTTT[G/T]AGCTGTCCTCACACC | 64326 |
rs115518291 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176168861 | ATAGTGTAGTGCTTA[C/G]AGCAGGAAAGAAAGA | 64326 |
rs115525590 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176031658 | ATTAGGAAAATCATA[A/C]CATAATTAGGAGGTT | 64326 |
rs115545673 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | RFWD2 | GRCh38.p7 | 1:176103389 | ATAAAACTCTATAAA[A/G]CTCCTAAACAATAAG | 64326 |
rs115597576 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | RFWD2 | GRCh38.p7 | 1:176052464 | AATTTCCCTCTTCCA[A/G]TCGATTTTAAAGACT | 64326 |
rs115604846 | snp | C/G | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175969124 | AATACCATGTTAACA[C/G]AAAAAGCAATACATT | 64326 |
rs115605077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176196787 | GTTCATGCCTATAAT[C/T]CCAGCACTTTGAGAG | 64326 |
rs115614909 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176186742 | TGTAGAAATGGTTAC[A/G]GAAGCTATCATAATC | 64326 |
rs115622001 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176025220 | GAACACTAAAGCTCA[G/T]TCAACTAAATGAAAT | 64326 |
rs115628706 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | RFWD2 | GRCh38.p7 | 1:176181926 | TGTATTATAATAAGG[A/T]TCTAAGCCTAAATTG | 64326 |
rs115641684 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:176173352 | AAAAAAAACCAGTAA[G/T]TGGCCAGGCACAATG | 64326 |
rs115660917 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176015064 | AATAGGCTTCTTTGA[A/G]GAGATGATGTTTAAG | 64326 |
rs115675355 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | RFWD2 | GRCh38.p7 | 1:175976467 | ATTTTTAGTGTAGAC[A/G]GGGTTTCAACATGTT | 64326 |
rs115676941 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | RFWD2 | GRCh38.p7 | 1:176158949 | CCTGGCCTAAGGTTC[C/T]TGTAATACAGATGAA | 64326 |
rs115678452 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176060691 | CAGGAAACCTTAAAA[C/T]TATGATATAAAGAAA | 64326 |
rs115687589 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176175806 | GGTATACAGTAGAGA[C/G]AGACTTGCTTACCAC | 64326 |
rs115688905 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176184965 | CCAATATTTTAACTC[C/G]GCACATAATTTTTAG | 64326 |
rs115689125 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:175960373 | AGCTAACAGAACCAT[C/T]TTTATGATCAAACAG | 64326 |
rs115724265 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant | RFWD2 | GRCh38.p7 | 1:176151848 | TTTCACTATAAATGA[A/G]TAATTTGGTCCTTAC | 64326 |
rs115724623 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176040953 | TTTATACACTTAATG[A/G]TGAGAAGAACCAGAC | 64326 |
rs115733366 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | RFWD2 | GRCh38.p7 | 1:176080234 | GAACTATATTAAAAT[A/G]GAAAAGTATCACATC | 64326 |
rs115736627 | snp | A/G | 0.00082203 | 0.0202568 | intron-variant | RFWD2 | GRCh38.p7 | 1:176175884 | ATCGAAATATTTTTA[A/G]AATAAAAATCATTCC | 64326 |
rs115744884 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | RFWD2 | GRCh38.p7 | 1:176096977 | TCCTTTTTGGTTTGA[C/T]ACCTGTGCAACCTTT | 64326 |
rs115745742 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | RFWD2 | GRCh38.p7 | 1:176198746 | ATGCAGAATACATAA[A/G]GAACACTTACAACGC | 64326 |
rs115747659 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176024247 | CTGGGCTCTGACAGA[A/G]TGAGACTGTCTCTAA | 64326 |
rs115748431 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | RFWD2 | GRCh38.p7 | 1:176189175 | AATAAAGATAAAAAC[A/G]GAAACAGACTTCTCA | 64326 |
rs115756907 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176131931 | CTAACCCATTTAACT[C/G]TGCTAGAATCTAATT | 64326 |
rs115763204 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:175984192 | CAGGCCTGGAGACCC[C/T]AGAGGAAAAAGTTGT | 64326 |
rs115797609 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | RFWD2 | GRCh38.p7 | 1:176169340 | TATTTGTTTGATCAA[C/T]TGTATACTACTACTA | 64326 |
rs115810311 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | RFWD2 | GRCh38.p7 | 1:176184284 | TAGCCTGCTTCACTG[C/T]GTTCTCCAACCTATC | 64326 |
rs115816582 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | RFWD2 | GRCh38.p7 | 1:176068772 | GTAGTCTATATAATT[G/T]AATATATGTGAATAA | 64326 |
rs115845968 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | RFWD2 | GRCh38.p7 | 1:175989946 | ACTCCGATAAGATCA[C/T]TCATTTGGCATCCAC | 64326 |
rs115853259 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176143618 | TATAAGCAAACCAAA[C/G]CATATAGAAGAGAAT | 64326 |
rs115873982 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | RFWD2 | GRCh38.p7 | 1:176048510 | GGATTTTAATGCACC[A/G]TAACTATAATGATGA | 64326 |
rs115913519 | snp | G/T | 0.021333 | 0.101051 | intron-variant | RFWD2 | GRCh38.p7 | 1:176146471 | AAGTTACAAAGAACA[G/T]GTGACTTCTGTCTTC | 64326 |
rs115914269 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | RFWD2 | GRCh38.p7 | 1:176106659 | CCCTATTATTTCATC[G/T]CCTACCTAACCAATC | 64326 |
rs115932362 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:175946580 | ACTGCTTATCTCAGG[A/G]TTTATTTATCCAATG | 64326 |
rs115947821 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | RFWD2 | GRCh38.p7 | 1:176123699 | TGTAACTTTACAGAG[C/T]AGAGTAAAAGAATTA | 64326 |
rs115970875 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | RFWD2 | GRCh38.p7 | 1:176078057 | AATCGATATTGCTAA[A/C]ATGGCAATATTGTTC | 64326 |
rs115982618 | snp | C/G | 0.0217236 | 0.101931 | intron-variant | RFWD2 | GRCh38.p7 | 1:176023069 | GATTCCTGATTCCGT[C/G]ATTACAGTAATGGCA | 64326 |
rs116006038 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176129961 | AAGCTAATGGCTTCA[C/T]AGGCTTAATAATAAG | 64326 |
rs116051399 | snp | A/G | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176177068 | AAACAGAAGCAACCT[A/G]AACACTAAGAAATTG | 64326 |
rs116059589 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | RFWD2 | GRCh38.p7 | 1:176117750 | AAGTAAAAAAATTAG[C/T]TGGGTGTGATGGCAA | 64326 |
rs116060242 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | RFWD2 | GRCh38.p7 | 1:176107683 | GATACAATGATAGAT[G/T]CTCAAAGGGAAGAAA | 64326 |
rs116086880 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:176022060 | TTTAATTAATGTATT[C/T]TGAGGCAATGTTATT | 64326 |
rs116088794 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | RFWD2 | GRCh38.p7 | 1:175949232 | CTATTAGAATTAACT[C/T]TGGAATATTATGGGC | 64326 |
rs116125747 | snp | C/T | 0.084728 | 0.187577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176094662 | TATCTTATTTGGTCA[C/T]TGGAAAAAGTTAAAA | 64326 |
rs116177481 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | RFWD2 | GRCh38.p7 | 1:176092137 | GATAAATCTGCAAGT[C/T]AACTGAGTTATGCAA | 64326 |
rs116177844 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | RFWD2 | GRCh38.p7 | 1:176141987 | TGATCCTCCTACCTT[C/T]GCCAACGTGTTAGAA | 64326 |
rs116180036 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant | RFWD2 | GRCh38.p7 | 1:176026266 | TCCATAAATGATGGC[A/C]AGTATGTTTATAAAA | 64326 |
rs116194675 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175949594 | CATCCAGAAAAGCAG[C/T]TGAAAATCTCACTGA | 64326 |
rs116207890 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176133690 | CAATTTCATAAAATC[C/T]AACAATCAGTGAGAG | 64326 |
rs116223035 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | RFWD2 | GRCh38.p7 | 1:176137157 | TAAGGGTTTTAAAAA[C/T]ATATTTGAGTTAGTA | 64326 |
rs116264356 | snp | G/T | 0.0023933 | 0.0345097 | downstream-variant-500B | RFWD2 | GRCh38.p7 | 1:175944340 | ATCCGGCCCTTTACA[G/T]AAAAAGTTTGCTGAC | 64326 |
rs116279271 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | RFWD2 | GRCh38.p7 | 1:176099895 | AACTCACAGGCATTT[G/T]AGGATACAAACTGAT | 64326 |
rs116279290 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175973702 | TATACATAATTTCTA[A/C]AATGGAAAAAAGTAA | 64326 |
rs116284017 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:176205990 | TAAGTGGCCCATCCT[C/T]TGAAATGGAAGAAGA | 64326 |
rs116284833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175975115 | CCTATTCAGAGCCAA[C/T]AGTTTCATTCTTAGT | 64326 |
rs116288987 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | RFWD2 | GRCh38.p7 | 1:175965772 | TTTTGTATTTGGAGA[C/T]GGGGTTTCATCATGT | 64326 |
rs116313932 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | RFWD2 | GRCh38.p7 | 1:176197209 | ATGACACAACAACAA[A/G]TGGCCCAACCTAGGC | 64326 |
rs116329506 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | RFWD2 | GRCh38.p7 | 1:175978826 | AGCTTCTATGTTGTC[C/T]TCTCCGCACTCATTG | 64326 |
rs116334529 | snp | C/T | 0.040671 | 0.13668 | intron-variant | RFWD2 | GRCh38.p7 | 1:176122615 | AACTCCAGAAAAAAA[C/T]TTCCCCAGCACCTCT | 64326 |
rs116388435 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | RFWD2 | GRCh38.p7 | 1:176012311 | ACTAAGTTTTTGTGG[A/G]GCTGGGGGTTTCACC | 64326 |
rs116403583 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | RFWD2 | GRCh38.p7 | 1:176079963 | AGGAGTCTGAGGATC[A/G]CCTAGGCAGCATAAT | 64326 |
rs116404978 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | RFWD2 | GRCh38.p7 | 1:176091780 | AAAACAGAAGTATAA[G/T]AAGTAAAACAGAATG | 64326 |
rs116456087 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | RFWD2 | GRCh38.p7 | 1:175980076 | TTTAACATTATAACA[A/T]CCCTAGAAGATAAGT | 64326 |
rs116476151 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176204814 | CCTGTAATCCCAGCT[A/G]CTACTCGGGAGGCTG | 64326 |
rs116484573 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176021663 | AATGGTTGTCTACAT[A/T]AACAATGATAGGAAA | 64326 |
rs116485888 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176035014 | TCTTACAATATAATA[C/T]TCAAAATGGCTAAGA | 64326 |
rs116494851 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | RFWD2 | GRCh38.p7 | 1:175948695 | TGGCATACAAGAAAA[C/T]AATAATGTCTTCCAC | 64326 |
rs116511871 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176038832 | CAAAAAAAAAAAAAA[A/G]AAAAGAAAAAGATAG | 64326 |
rs116527210 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176125061 | TTGCCATGTTTGTCT[C/T]GAGAAATGTCTAATC | 64326 |
rs116585942 | snp | C/T | 0.0185938 | 0.0946107 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207935 | ATTTTATTAGTTCGA[C/T]CACGACTTCACTCCT | 64326 |
rs116592214 | snp | A/C | 0.0345262 | 0.126772 | intron-variant | RFWD2 | GRCh38.p7 | 1:176098032 | TTATTGGTAAAATAC[A/C]GATGTCATCAAAATG | 64326 |
rs116592593 | snp | C/T | 0.0228947 | 0.104514 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176144926 | AAATAAAGAACAGCA[C/T]AGAAAAATGTCTTCA | 64326 |
rs116593726 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | RFWD2 | GRCh38.p7 | 1:176152716 | AAAGTGCCGTAATTA[C/T]GGCGTGAGCCACTGT | 64326 |
rs116603231 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RFWD2 | GRCh38.p7 | 1:176179147 | AATACAAGAATTAGC[A/G]GGCATATTGGTGCAC | 64326 |
rs116605721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176052900 | CACATATGAGAGCAA[C/T]CTCATTTTTGTCTCC | 64326 |
rs116610063 | snp | C/G | 0.0217236 | 0.101931 | intron-variant | RFWD2 | GRCh38.p7 | 1:176129897 | GCTAACGTTCCTCAT[C/G]ACACCAGATTTACAG | 64326 |
rs116611013 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176021281 | AAATATAAAATCCAG[C/T]ATGCCCACACCAGAA | 64326 |
rs116618089 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | RFWD2 | GRCh38.p7 | 1:175984967 | TTTACAGACTCATAG[A/G]CAGAAGGGACTTGGC | 64326 |
rs116643409 | snp | C/T | 0.00482856 | 0.0488975 | intron-variant | RFWD2 | GRCh38.p7 | 1:176168743 | GGAGCAGACAGAGTA[C/T]GCACACTGGAGGGAA | 64326 |
rs116646124 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | RFWD2 | GRCh38.p7 | 1:175977563 | TTAAGAAATAATGGA[A/G]TAAGAGATAAAAAAG | 64326 |
rs116674042 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | RFWD2 | GRCh38.p7 | 1:176101268 | AACACCTCACTTTCC[C/T]TCCCTCAAATACTCC | 64326 |
rs116680519 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:175962519 | TAAATGGTATAAAAA[C/G]CTCCAAACCGAGCCT | 64326 |
rs116693477 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:175979771 | AATGGTAATTGATTA[A/T]TACCATTTAGTTTCA | 64326 |
rs116746072 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | RFWD2 | GRCh38.p7 | 1:176108758 | TGAATGTGTGAATTT[C/T]TGTCTTTTAAAAATA | 64326 |
rs116750954 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | RFWD2 | GRCh38.p7 | 1:176159517 | CGAGCACAAGGAGAA[A/G]GGTATACTAAATGTA | 64326 |
rs116767830 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176103862 | TTCTCCCTGAGATAA[C/T]TGGTAAGATAAAGGC | 64326 |
rs116772510 | snp | A/G | 0.0170251 | 0.090679 | intron-variant, downstream-variant-500B | RFWD2 | GRCh38.p7 | 1:175967307 | GTGAGCCACCGCGCC[A/G]TTGAAAGCTCATCTC | 64326 |
rs116773030 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | RFWD2 | GRCh38.p7 | 1:176042089 | TGTACTCCAGTCTGG[A/G]CAGCAGAGCGAGATT | 64326 |
rs116780520 | snp | A/T | 0.0248432 | 0.108648 | intron-variant | RFWD2 | GRCh38.p7 | 1:176159082 | GCATCTAAAATGGAA[A/T]CACCTAAAATCATGT | 64326 |
rs116801772 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176155520 | AACATTATAACAACA[C/T]ATGACTAGAAACCTA | 64326 |
rs116806464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176144985 | GTGACACAAAACACA[C/T]TAAGTATAACAGATA | 64326 |
rs116831883 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | RFWD2 | GRCh38.p7 | 1:176179562 | AATGTGGTGAAACCC[C/T]AACTCTAAAAAAATT | 64326 |
rs116836240 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | RFWD2 | GRCh38.p7 | 1:176119091 | TGTCATGAGTTTATT[C/T]TGATAAAATGTAACC | 64326 |
rs116838130 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant, utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175967596 | TCCCCACAACTTAAC[A/G]GCAAAACACACAACA | 64326 |
rs116985956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176052714 | CAATTGCCCTCTCTG[C/T]AGGCAACCAATAATT | 64326 |
rs117101883 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | RFWD2 | GRCh38.p7 | 1:176000161 | GCTTGTGGGATATTA[C/G]TAAAGAAATTTTTGC | 64326 |
rs117390399 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176072406 | CCTAGATGAATCTCT[C/T]AGCCTAAAACACAGC | 64326 |
rs117595976 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176200733 | TGAATATATTGTTTG[A/G]GAAAGTACCAACCTA | 64326 |
rs117608180 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176086090 | CATTCGCAGAATGAT[A/T]AAAACTAATAATGAC | 64326 |
rs117625501 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176077278 | GTAAGCTGAATCCAG[A/G]AGCACATCAAAAGTT | 64326 |
rs117805422 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | RFWD2 | GRCh38.p7 | 1:175983580 | CAGAAGTGGGGTGCT[A/G]CTGAAAAGATACCCC | 64326 |
rs117857217 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | RFWD2 | GRCh38.p7 | 1:176202313 | TCCCATCTCAGCTTC[C/T]TGAGTAGCTGGGACT | 64326 |
rs118028361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176020539 | AAAGATTAGCCAGGC[A/G]AGGTAGTGCATGCCT | 64326 |
rs118066530 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176012031 | AAACTGTAATACAAC[C/T]TCAGGAAGCTGGGCA | 64326 |
rs118084939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176139434 | TATTAAAAGAGAACT[A/G]CTATTTGACCGAGTA | 64326 |
rs118100939 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | RFWD2 | GRCh38.p7 | 1:176179788 | ATTATTCCAAAATCT[A/T]GTAGAAAATCCTCTT | 64326 |
rs118141430 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | RFWD2 | GRCh38.p7 | 1:175981081 | TCTCTAGATAAATCA[A/G]TGTTAATAAAAAAGA | 64326 |
rs137857237 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | RFWD2 | GRCh38.p7 | 1:176128904 | TAGGTAATAATCCAG[C/T]CAAAGACTCACTATG | 64326 |
rs137869412 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176065582 | TGAGCTGAGGACAAT[A/G]GAAAAAGAGTAAACA | 64326 |
rs137869965 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | RFWD2 | GRCh38.p7 | 1:176043046 | AAAACAAAACAAAAC[A/C]ACATGGGGAATAATA | 64326 |
rs137876804 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | RFWD2 | GRCh38.p7 | 1:176003653 | TTTGTCAGAGATCAG[A/G]TAGTTGTAGATACGT | 64326 |
rs137899056 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175985648 | CTCACAGGGGAAAAG[C/T]AGATTCAAAAGCCAG | 64326 |
rs137921574 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176169678 | TCATAATCTTTTTGC[C/T]GGTAGAGAGTCTTGC | 64326 |
rs137929206 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176040299 | CCTTCTCCCTCTCTG[C/T]ACCACCCCCTTTTCC | 64326 |
rs137929481 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176076129 | ACCAACTGGATACAC[A/G]TTGACACAGAGTACT | 64326 |
rs137931910 | in-del | -/TATAA | 0.00953873 | 0.0683987 | intron-variant | RFWD2 | GRCh38.p7 | 1:176162302 | AAGGTGTGTGTTGCT[-/TATAA]TATATCACACTCAAT | 64326 |
rs137933386 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:175982067 | GAGAACTCTTGTAAC[A/G]TTGGTGGGAATGTAA | 64326 |
rs137958168 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175957888 | CACAAGCATTTCAAA[A/G]TATCATGCTAAATAA | 64326 |
rs137971403 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176100739 | CAAATCTTAGCAGGC[A/G]TAACTATATCCACCA | 64326 |
rs137978301 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176015326 | AGAGGTTACTCCAGT[A/G]GTAAAGGTAATGTAA | 64326 |
rs137983700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176069251 | ACGTGGTTTTGGACA[C/T]AATGAAGCAATAAAA | 64326 |
rs138026194 | in-del | -/TG | 0.0689305 | 0.172377 | intron-variant | RFWD2 | GRCh38.p7 | 1:175980016 | ATGTATCGCTTTTGC[-/TG]TGTATCAGGAACTGT | 64326 |
rs138028795 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992048 | TATTGTGTAGTATAC[A/G]TAATCGTATGTGCTA | 64326 |
rs138043577 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176173417 | GAGGCAGGAGGATCA[C/T]TGGAGCCCAGGAGTT | 64326 |
rs138045186 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:176103952 | TTCCTATGAAAAAAC[A/C]AACAGGAAGAAATAT | 64326 |
rs138078582 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:176043648 | AAGGCACATGAAGTT[A/C]TAAAAGTTTTAACAA | 64326 |
rs138086992 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | RFWD2 | GRCh38.p7 | 1:175961100 | GACTCTGGGACTTGC[A/C]TCAATGGGCCCTCAA | 64326 |
rs138087933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176055003 | GTCAACTCCGAATTC[C/T]GACCTTCCTTAAATA | 64326 |
rs138094586 | snp | A/C | 0.197703 | 0.244469 | intron-variant | RFWD2 | GRCh38.p7 | 1:175994217 | TCTGTCACCACCAGG[A/C]CTGCCCTAAAAGAGC | 64326 |
rs138105928 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176142491 | CTAAAAGATAATGAG[A/C]CAGTAATAGGTATAA | 64326 |
rs138130402 | snp | C/G | 0.0275645 | 0.114116 | intron-variant | RFWD2 | GRCh38.p7 | 1:175993315 | AAAGCAGAAAAACTG[C/G]AAACTCTAAAAAGCA | 64326 |
rs138138273 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:175989801 | ATTTGTTTTAAAAAA[C/T]CATTATTTAGATATA | 64326 |
rs138153342 | snp | C/G | 0.0174175 | 0.0916809 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207677 | CACATTCCGGAACGG[C/G]AAGAAGGAGCTGTCT | 64326 |
rs138189989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176028600 | ATCAATATAGATAAA[C/T]GATAAATTTATACTC | 64326 |
rs138191062 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176079544 | TGTACCTATGCTCAC[C/T]GTCTGGGTGACGGAA | 64326 |
rs138195383 | snp | C/T | 0.167484 | 0.23599 | intron-variant | RFWD2 | GRCh38.p7 | 1:176019235 | TTTGGGAGGCCGAGG[C/T]GGGCGGATCACGAGG | 64326 |
rs138207847 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176016668 | ATTTCCATTCAAAAA[C/G]TATTTTGTATGGAAT | 64326 |
rs138225692 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176182168 | AGTTACAGGACACTC[A/G]AGAAAATTAAAAACC | 64326 |
rs138238549 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176076617 | GAAGAAAAAACTAAA[A/G]TCAGAGAAGAGCTGA | 64326 |
rs138239055 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176148186 | GAGAATAAGAAAAAT[A/C]TAGTCACAAACCACA | 64326 |
rs138240390 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176114173 | TCTCTCAAGTTCCTA[C/T]GGTATATTTCAATTT | 64326 |
rs138250665 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175969026 | CTCTGAGCATAGAAC[C/T]GTGCATATTTAAGAG | 64326 |
rs138255422 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176033074 | TAAAATCTACCAAGA[C/T]TTCACAGTTGTCACT | 64326 |
rs138270969 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | RFWD2 | GRCh38.p7 | 1:176184389 | CCTATTAACAATTAA[G/T]AAACGCAGAAGTTTT | 64326 |
rs138278471 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175947699 | AACATGTTTTTAACT[A/G]TATTTTAAACTTAAG | 64326 |
rs138280470 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176195785 | GGATTAACACAAAAA[C/G]AGAAAACCAAATACC | 64326 |
rs138316488 | snp | A/G/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176128077 | ATTTTAAAAATAGGG[A/G/T]TGTTTCATTGAGTAT | 64326 |
rs138360905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176119409 | TGATATCTCAGTGTA[C/T]ACAGTGATATAATTC | 64326 |
rs138372117 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | RFWD2 | GRCh38.p7 | 1:176115735 | TGGAGACAGTGAGAT[C/T]CTGTTTCAAAAAAAT | 64326 |
rs138374160 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176161349 | ATCCCAGCACCCTGG[G/T]AGGCTGAGGTGGGAG | 64326 |
rs138393250 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176133115 | CACATATGTACGTAT[A/G]TATACTATATATACC | 64326 |
rs138397733 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175977766 | CTAAGCAAAACATAC[A/T]TATTTTTGCTTAGTT | 64326 |
rs138406127 | snp | A/G/T | 0.000149986 | 0.00865856 | missense | RFWD2 | GRCh38.p7 | 1:176085785 | ATATACCTGAGATAC[A/G/T]AGACATCCTTGTAGA | 64326 |
rs138406243 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175976809 | AAAATATTTAGATAG[C/T]TCGTAATGAAATAAG | 64326 |
rs138427173 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176157831 | TCAATCTATATGGAG[A/C]AAAATTGAAGACAGC | 64326 |
rs138431599 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RFWD2 | GRCh38.p7 | 1:176068507 | GTAAGAACGACTAAC[A/G]TTTACGTAGTATTTA | 64326 |
rs138472118 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176018145 | GCACTAATGTTAGCT[A/G]TTATTATTTACCCTT | 64326 |
rs138498164 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:175972238 | CTATCCCAAGTAACT[A/C]ATAATTCTAAAGCAG | 64326 |
rs138528922 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:176065275 | AAATTAACTCAGACA[A/G]AGGGGAAAAAAACTG | 64326 |
rs138536494 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | RFWD2 | GRCh38.p7 | 1:176002418 | GTGCAGGTTAGTTAC[A/G]TATGTATACATGTGC | 64326 |
rs138540197 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | RFWD2 | GRCh38.p7 | 1:176009742 | TGATTTTATATATTG[C/T]ATTTATTAATAATTA | 64326 |
rs138544614 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176000753 | TTGTTATGTCATTTG[A/C]TCTTTTATGCCTCCA | 64326 |
rs138545182 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176173199 | ACCTATAATCCCAGC[A/T]ACTAGGGAGGCTGAG | 64326 |
rs138546730 | in-del | -/CAGTATATTAATTCATT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175980290 | AAATACAATACAAGA[-/CAGTATATTAATTCATT]CAGTATATTAATTCA | 64326 |
rs138582810 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | RFWD2 | GRCh38.p7 | 1:176007081 | CTAAACTTCCCATCT[C/T]GCTTCATTTCATTCA | 64326 |
rs138589561 | snp | A/C | 0.0217236 | 0.101931 | intron-variant | RFWD2 | GRCh38.p7 | 1:176168799 | GAGAAAATGCTGTGG[A/C]AGGTAGAGAAAGATG | 64326 |
rs138590545 | snp | A/T | 0.021333 | 0.101051 | intron-variant | RFWD2 | GRCh38.p7 | 1:175949801 | TGGGTCTAGTCACCT[A/T]TTAATATAGAGAAGG | 64326 |
rs138598520 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176061977 | AGGAATTCTCATCAC[C/T]AAACAAGAGAAAGAC | 64326 |
rs138598610 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176100129 | GTGCGGTGGCTCACG[C/T]CTGTAATCCTAGCAC | 64326 |
rs138607193 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176165443 | ATCAATATAGTCATC[C/T]CAGCACTTTGGGAGG | 64326 |
rs138607538 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176095292 | GAATAGTGGTTATCA[C/T]AGTGTGATCCCCAAA | 64326 |
rs138621101 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176103476 | ATGCATGCCCAGAGA[C/G]GGCATGGAAGCTCTG | 64326 |
rs138631703 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176141851 | TTCTCTCACCTCAGC[A/C]TCCCAAGTAGCGGGG | 64326 |
rs138639525 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176101199 | GACACCCATGGGTGG[C/T]ACCCTATCGTGGCTG | 64326 |
rs138650062 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | RFWD2 | GRCh38.p7 | 1:176023129 | GCTGAGAAATAACAG[C/T]TCTCCTGGCCTATCT | 64326 |
rs138664798 | snp | C/G | | | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207357 | TCAGACGCTCAGGGC[C/G]CGCCCTCGGGGTCGG | 64326 |
rs138668228 | snp | C/T | 4.9597e-05 | 0.00497956 | missense, synonymous-codon, intron-variant, utr-variant-5-prime | RFWD2 | GRCh38.p7 | 1:176175946 | GGTCAATATTGTCCA[C/T]AACATAGTTACACTT | 64326 |
rs138672050 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176108715 | GCTTTTATTTATTTG[C/T]AAAAATTGAGTATTA | 64326 |
rs138678133 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176202536 | GTGTTTTTCAGACTA[C/T]TAAAAATATCCTGGG | 64326 |
rs138688529 | in-del | -/CT | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:176127220 | AGAACATTTAAAATC[-/CT]CTCTTTTGCTATTCT | 64326 |
rs138691914 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | RFWD2 | GRCh38.p7 | 1:176057385 | TCCCTCTGATGCCGA[A/G]CGGAAGCTGAACTGT | 64326 |
rs138694975 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176138331 | GGGCAAAGGAAGAAG[C/T]AGCATTAACAATCAA | 64326 |
rs138742788 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175960280 | GCTCTAACGCTTCTA[A/G]ACTTTTCATTATGGG | 64326 |
rs138755500 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176196638 | AAATATATGAAGACC[C/T]AAAACTATGGCTTCA | 64326 |
rs138767936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175965239 | GATCCTACAGCCACA[A/G]AACAATTTCAAATAA | 64326 |
rs138817834 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175969196 | TCCTTTTAGACATTC[A/C]ATTTCTCCAAATATA | 64326 |
rs138840702 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | RFWD2 | GRCh38.p7 | 1:176112779 | GAGATCCACTTTTTT[A/T]TGGCTCCCATTTAAG | 64326 |
rs138861202 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175958232 | CACAAGAACAAATAC[A/G]TATTTTATAAGTTAA | 64326 |
rs138861754 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175994353 | AACGAGCAAAATAAC[A/C]AGTTAACATCATAAT | 64326 |
rs138875167 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176061543 | AGGCAGGAGAATCAC[C/T]TGAACCCCGGAGGCA | 64326 |
rs138889919 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | RFWD2 | GRCh38.p7 | 1:176153726 | GTTGGCTGTGGGTTT[C/G]TCACAGATGGCCCTT | 64326 |
rs138901622 | in-del | -/TCTATGTCTTCTTT | 0.405429 | 0.195811 | intron-variant | RFWD2 | GRCh38.p7 | 1:176128005 | GCCTCTTTTTCTATA[-/TCTATGTCTTCTTT]TCTATGTCTTCTTTT | 64326 |
rs138903942 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176165346 | TTCAGGTGAGAGAGA[C/G]AGAGAGATGTGTGTC | 64326 |
rs138909538 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175980481 | GAAAACAAAGGTGCA[C/T]AGTTATAACTGCATA | 64326 |
rs138913087 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | RFWD2 | GRCh38.p7 | 1:176052541 | CCCCATTTACTACTA[C/T]GTAAAATTCAGACTC | 64326 |
rs138914046 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | RFWD2 | GRCh38.p7 | 1:176087458 | AGGGTATGAACACAC[A/G]CTTCTCAAAAGAAGA | 64326 |
rs138923127 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992210 | AGCATTTATCCTTTG[C/T]GTTACAATCTAATTA | 64326 |
rs138928350 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176124725 | GAACAGTGCTGCAAC[A/G]AACATGGGAATGCAG | 64326 |
rs138937636 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175990157 | GTGTTTCCATTTTCA[A/T]TCAGTTTAAAATCCT | 64326 |
rs138949679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175972513 | CTGTGTTGCCAGAAT[A/G]GAGTGCAGTGGTGTG | 64326 |
rs138960406 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176191790 | AGATTAAACTTATTT[C/G]GTATTTTGTGAAGTG | 64326 |
rs138967522 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:176188777 | AACCTGCTATTTCCC[C/T]CCTCTCTTCCTCTCC | 64326 |
rs138974358 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176152497 | CTGTTTCCCAGGCTG[C/G]AGTACAGTAGCACGA | 64326 |
rs138976538 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176083507 | TGTTTGCGTGGTGTT[C/T]TATCATCAACATCCA | 64326 |
rs138986781 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176147660 | AAAAGTTCTACGGCA[C/T]GATTCATCCAGAAGT | 64326 |
rs138992757 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176079814 | TTATGTGAGGAATTA[G/T]TCCATTCTCTCCATT | 64326 |
rs139025867 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175948744 | GGAATCAGAATACTC[C/T]TTGGAATTAGTCAGC | 64326 |
rs139032433 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RFWD2 | GRCh38.p7 | 1:176158386 | CTGCACTAAAGAAAT[A/G]GTAAATGATGTCCTT | 64326 |
rs139053551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176182956 | TAACCTCTGAGGAGG[C/T]AGGTAAGAAAAACTA | 64326 |
rs139086855 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176180042 | CGTATCTTAGAGCAT[A/C]TACTACTTCACTACC | 64326 |
rs139088499 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176113271 | GATATCTCATTGTGG[A/T]TTTGACTTCCACTTC | 64326 |
rs139120336 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | RFWD2 | GRCh38.p7 | 1:175998685 | ATAGTTCATAATGTA[C/T]AATAGTCCAGAGATG | 64326 |
rs139123395 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176091705 | GAACAGGTAACAATC[A/G]AACCAGAAGAGGGAT | 64326 |
rs139125936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176034784 | ACCCAAGTCCTAAAC[C/T]AAGCTCTAACTGGCA | 64326 |
rs139139062 | snp | A/G | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176186169 | CACTGAATATGTCAG[A/G]AGCTATTTAATAGAA | 64326 |
rs139153881 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | RFWD2 | GRCh38.p7 | 1:176002105 | GGTTTATTGAGCTTT[C/T]TGGATGTGTGGATTG | 64326 |
rs139156446 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176130378 | ATTTTCTCATTATTT[C/G]ACACACACAACTATG | 64326 |
rs139161935 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:175950328 | ACATCCTCTCTCCCC[A/G]AAGGTAGTATGATTA | 64326 |
rs139169269 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176179425 | GACAAGAACAAGCTA[A/G]GCTGTTAAGTCAGAG | 64326 |
rs139207053 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:175978726 | AAGTGTTATAAACAA[G/T]CCAGTCAGAGGAAAG | 64326 |
rs139216998 | in-del | -/AAAAAAAACAAAA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176139280 | TGAAAAAACAAAAAC[-/AAAAAAAACAAAA]AAAAAAAACAAAAAA | 64326 |
rs139229940 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176038786 | TCATATCATTGCACT[A/C]CAGCCTGAGCAACAG | 64326 |
rs139258179 | snp | A/G | 0.000376648 | 0.0137179 | intron-variant, missense | RFWD2 | GRCh38.p7 | 1:176133850 | GTATGTACTTACATA[A/G]TAAGTATTCCATTGA | 64326 |
rs139264375 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176071266 | TAGCTATGTGACTTG[C/T]CTGCTCCCACTTCAC | 64326 |
rs139267336 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | RFWD2 | GRCh38.p7 | 1:175954856 | AAGATAATTCAGTCA[C/T]ATACAAAAAGAATAA | 64326 |
rs139270293 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176000402 | TTGTCAAAAATGAGT[G/T]CACTGTAGGTGTGCT | 64326 |
rs139290626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176174235 | AAGAGTAAGTAGTTT[C/T]CCAAAGTTATGACTA | 64326 |
rs139300663 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175990519 | TGACAATGTTATTCA[A/T]GTCTTCTAAAACTCT | 64326 |
rs139324654 | snp | C/G | 0.0217236 | 0.101931 | intron-variant | RFWD2 | GRCh38.p7 | 1:176093928 | CTCGGGAGGCTCAGG[C/G]AGGAGAACCACTTTA | 64326 |
rs139326571 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176080072 | AGCCTCAGTAATCAT[A/G]GGTCGAAGAGAAAAA | 64326 |
rs139328079 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176066026 | CCACCGCACCTGGCC[A/G]GGGGATAATGATTTT | 64326 |
rs139337315 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176036976 | GAACTGTCAAAAATT[A/T]CACTCAAGAAGAGAC | 64326 |
rs139351574 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176033628 | TATATTTCTCCAAAA[G/T]AACCTTTAAAATGAC | 64326 |
rs139373171 | snp | C/G | 0.00026575 | 0.0115241 | missense, intron-variant | RFWD2 | GRCh38.p7 | 1:176149051 | GAATTCCATAAGAAT[C/G]TGTAGTTGGGCTGCA | 64326 |
rs139389222 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | RFWD2 | GRCh38.p7 | 1:176132277 | ATCATAATTAGTCTT[C/T]ACTTGATTAATGTGT | 64326 |
rs139396063 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176177152 | ACAAATTATTGTAAT[C/T]TGTATGCCATAAAAA | 64326 |
rs139415140 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176030382 | GGTAATTCACAATAG[A/G]TAAGTATGGAGCACT | 64326 |
rs139425528 | snp | A/G | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175969671 | TTCTGTGTCACGTAA[A/G]ACTTCTATGTCATGT | 64326 |
rs139432280 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176085656 | TGATGATCTGGTAGA[C/G]TATGTCAAAAATACA | 64326 |
rs139436166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176025720 | CATGGCAAAACCTCA[C/T]CTCTACGAAAAATAC | 64326 |
rs139438407 | snp | A/C/T | 0.0107347 | 0.0725747 | intron-variant | RFWD2 | GRCh38.p7 | 1:176120294 | GCATCATGGCAAGTG[A/C/T]GTGTAATCCCAGATA | 64326 |
rs139440924 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176170475 | CTCCTTTGTACATCT[C/G]TATCAGAGCTCTTGG | 64326 |
rs139444880 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176101321 | GGAACCTGGGGCACC[A/G]TGCTCCTCTCTTTCT | 64326 |
rs139446794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176063891 | CCAAGTGACAGGTTA[C/T]TACTGTTAAGTAAGT | 64326 |
rs139447523 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175992782 | CCACAGCTCAAGGAG[A/G]CCTGCCTGCCTCTGT | 64326 |
rs139456548 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176189443 | ACAAAAATACTTCTT[C/T]AAAATACTAAGAGAA | 64326 |
rs139470112 | in-del | -/AATAA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176077916 | ATAGCCACAAAGAAA[-/AATAA]ATAACTAGGAACTCA | 64326 |
rs139471229 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176125163 | GGTTATTAATCCCTT[A/G]TCAGATGAGTAGTCT | 64326 |
rs139490334 | in-del | -/GA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176165338 | AAGAAAAATTCAGGT[-/GA]GAGAGAGAGAGAGAT | 64326 |
rs139504354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176167071 | TTTATTATTTTTGTA[C/T]TTCAAAAATTTAACA | 64326 |
rs139508019 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176203389 | CTTACTATCTACATG[C/G]AAACGTATACTTCTG | 64326 |
rs139512354 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | RFWD2 | GRCh38.p7 | 1:176097585 | AGCTTTTTTTATAGA[C/T]TGGCTGGGTGCAGCA | 64326 |
rs139517769 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175970214 | CTATAGGTTCATCAA[C/T]AGCTGTGAGAAACCA | 64326 |
rs139518615 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176200533 | AAACCACACAGATTA[A/G]GAAAGAAGGATGGAT | 64326 |
rs139533007 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176062493 | ATAACAATGCTAAGA[A/G]TTGCTGAGGATTTAG | 64326 |
rs139534629 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176026079 | TTACATGGAAAATTA[A/G]ATGAGAAAAATAACT | 64326 |
rs139540633 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | RFWD2 | GRCh38.p7 | 1:176031382 | AGGCGATCCTCAAAA[A/T]AAGGAGACAGTATAC | 64326 |
rs139544984 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, downstream-variant-500B | RFWD2 | GRCh38.p7 | 1:175967477 | GGTGACACAGTGAGA[C/T]TCAGTCTCAAAAAAC | 64326 |
rs139547674 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176062939 | GAAATTTTTAAATGG[C/T]TGAATTATTGTATAG | 64326 |
rs139555635 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175982722 | TATATAATGGAATAC[C/T]ATTCAGCTTTACATG | 64326 |
rs139565800 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176154733 | TACAATGAACCCCCA[C/T]GACACAAGTTTACCT | 64326 |
rs139566789 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176125342 | TGCCCCAAGTTTCCC[C/T]AATGTTTTCTTGTAG | 64326 |
rs139574206 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176166155 | TTATTGAGACAGGGT[A/G]TGACTCTGTCACGCA | 64326 |
rs139583090 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176197549 | TGTTGTATTTTGTTA[C/T]GGCAGCCCAAGCAAA | 64326 |
rs139596116 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | RFWD2 | GRCh38.p7 | 1:176120930 | CGATGAGCAAAAATA[A/G]AGCACACTGAGATCA | 64326 |
rs139598295 | snp | C/G/T | 0.00518141 | 0.0506816 | intron-variant | RFWD2 | GRCh38.p7 | 1:176059835 | TTCATTTATGAACAC[C/G/T]AGAATCTGAATTTTC | 64326 |
rs139614705 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176010987 | TACATTTTTAAGGCT[A/G]ATTTTTAATTGTGAG | 64326 |
rs139623288 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176020496 | CCAGCCTGGCCAACA[G/T]GGTGAAACCCCATCT | 64326 |
rs139629782 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175961822 | AGGTCACAAATGGAA[C/G]AATGGAAGAATAAAA | 64326 |
rs139652200 | in-del | -/A | 0.0663309 | 0.169604 | intron-variant | RFWD2 | GRCh38.p7 | 1:176084691 | CTTGGTCTTCAGAGG[-/A]AAAATGCTTTGTAAA | 64326 |
rs139660050 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176017365 | TTATAAAAGTCCTCA[A/T]TGCCCTAGCTTTTGG | 64326 |
rs139660113 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176055534 | CTTTGGTGATCTCAT[A/G]TAGTCTCATGACTTT | 64326 |
rs139663373 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176163307 | TCAATTTTGCATGTA[A/G]TAAGGTATTAAGCTC | 64326 |
rs139668989 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176066231 | AAGCCTAGCCATTTC[G/T]TTGGGGTTCTCCCTT | 64326 |
rs139673249 | snp | A/C/T | 0.0111196 | 0.0737302 | intron-variant | RFWD2 | GRCh38.p7 | 1:176004835 | GGTTGTGTCTCTGCC[A/C/T]GGCTTTGGTGTCAGC | 64326 |
rs139676046 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176159619 | AGATTACTATAAGAA[G/T]TTAAAATAAATAAAC | 64326 |
rs139698398 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176170853 | CTGTTAGGCAAGGCG[C/T]GATAGCTCACGCCTG | 64326 |
rs139699342 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176101797 | GCAACCGAAGCCTCA[G/T]ATGATGGCCCCTTTT | 64326 |
rs139711744 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176113001 | TCCAAATATTGGCTA[C/T]TGTGAATAGTGCTGC | 64326 |
rs139746655 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176053648 | CCTCCTTCACCTTAT[G/T]ACATAACACTTTCTG | 64326 |
rs139749254 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176203879 | CAACAGTTCTCAAGG[A/T]GGGGAGAAGGACAGG | 64326 |
rs139757278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176017196 | TATTAATGAGGCAAC[A/G]TTTTAAAATACAGAT | 64326 |
rs139760010 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175986119 | CTGCCTCGCGGGTTG[A/T]TGCCATTCTCCTGAC | 64326 |
rs139768760 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:175959028 | GGAAAAGATTATAGG[A/C]CAATGTTATTCATAA | 64326 |
rs139771546 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | RFWD2 | GRCh38.p7 | 1:175983314 | GGGCAAGTCTTTCCC[A/G]AACTGTTCTCGTGAC | 64326 |
rs139774134 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176154035 | GATGTGAATCAGTAA[C/T]ACTGGTCTTAAGTTT | 64326 |
rs139780006 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176051043 | CAGCCTGTGCAACAA[G/T]TTAAACACAAAGGGA | 64326 |
rs139807398 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176150602 | CTAGAGGACAAAGAC[A/C]ACATGTTTATTTAAA | 64326 |
rs139813573 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176185583 | AACAAAAATGCAAAA[C/T]CTTGTAAAAAGACAT | 64326 |
rs139824255 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | RFWD2 | GRCh38.p7 | 1:176053009 | TAAACAATGCTGGGG[A/G]AAAAAAAAACCCCTT | 64326 |
rs139826959 | snp | A/T | 0.0217236 | 0.101931 | intron-variant | RFWD2 | GRCh38.p7 | 1:176074752 | GCAATAATGAAACCA[A/T]CTCTTCCCCAAAATC | 64326 |
rs139835306 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176012535 | ACAAAGAACTATTAA[A/C]AAATAAATTTAGTAT | 64326 |
rs139866662 | snp | A/G | 0.0894459 | 0.191631 | intron-variant | RFWD2 | GRCh38.p7 | 1:176003920 | GATGGGGATGGCATT[A/G]AATCTGTAAATTACC | 64326 |
rs139895086 | in-del | -/A | 0.180064 | 0.240019 | intron-variant | RFWD2 | GRCh38.p7 | 1:175998484 | AAATTAAAAAAAGAG[-/A]AAAAAAAGAAAAAAA | 64326 |
rs139897208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176109192 | TTGCCCTAATTATGA[C/T]GCCTTTCTCAATTTG | 64326 |
rs139900138 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176105642 | AGCATGGATTGACCT[C/T]AGCTTGTATGGACTG | 64326 |
rs139900948 | snp | A/C | 0.0368353 | 0.130617 | intron-variant | RFWD2 | GRCh38.p7 | 1:176001647 | CTTTACAAAAAAATT[A/C]ATCTAAACTATCTTT | 64326 |
rs139905169 | snp | A/G | 3.31647e-05 | 0.00407201 | missense | RFWD2 | GRCh38.p7 | 1:175989426 | TACGGTGTCCTTTGA[A/G]TACCATGATTGGCTG | 64326 |
rs139930978 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176096762 | TAACTATGAAAAAGG[A/T]TTTATATTGGTCTTA | 64326 |
rs139953931 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176009108 | CTACAGCTAGGTACA[C/T]GTCAGAGCTTCTTGA | 64326 |
rs139977160 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175963324 | TCTCAATAAAGTCCC[C/T]ACTCCACCATCCTAC | 64326 |
rs139990064 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176133238 | TACGTACGTATATGT[A/G]CGTAGGTACACACAT | 64326 |
rs139990310 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | RFWD2 | GRCh38.p7 | 1:176092322 | GATAATATGTTTACA[A/G]TCTTGAGAAAGGGCA | 64326 |
rs139990429 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175994960 | TTTTTCAGCACCACA[C/T]AACACCTATTCCAAA | 64326 |
rs140015262 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176197146 | ATCCAATACAACCAG[G/T]ATTCTTCTAAGATAC | 64326 |
rs140016905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176105465 | ATATCTCTAGTTACA[C/T]TGGTTTTCTCAGCAA | 64326 |
rs140017543 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176144870 | CAAAAATAAATCTTC[A/G]AGTATAGATCTAAAT | 64326 |
rs140022848 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | RFWD2 | GRCh38.p7 | 1:176044657 | TTTAGGTAGACTTGA[C/G]TTCAAATTCCAGATC | 64326 |
rs140023190 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176130875 | GAATCAAAATAAGTA[A/G]AAATCTTTACAAAAC | 64326 |
rs140029946 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176056178 | AAATGTTAATTTTTA[C/T]TTTCTGTAATTTGAG | 64326 |
rs140058414 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:175957530 | ATGTTTGTGCAATGA[C/T]GAAATCAAATCACCT | 64326 |
rs140063874 | snp | A/T | 0.00358779 | 0.0422022 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176208668 | AAAATGAGAATTACA[A/T]AATTGTTTTTAAACC | 64326 |
rs140082993 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176144657 | TTCAAAGCTCTAGTA[C/T]TTAATACAAGGTGGT | 64326 |
rs140086149 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176100655 | ATAAACAGAATGCCC[A/G]TCACTCGGAGGTTTC | 64326 |
rs140089338 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176205339 | CAGATTAATTCTGAT[A/C]AAGAATAACGTACAA | 64326 |
rs140094679 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176140636 | TGTAAACATAACCCC[A/G]GGAAGGAGAACTTAG | 64326 |
rs140113658 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175991049 | AGTGCCAACATTTCA[A/T]TCAAAGCTCCAAATG | 64326 |
rs140115176 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176051321 | TACAGTTATGTGCTA[C/T]TTAAGGACATCTTAT | 64326 |
rs140162811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176151678 | TGATCAGAGCCTAAT[A/G]TAATTAAATATGTGA | 64326 |
rs140170825 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176020756 | CAAATAATTTAAAAT[G/T]TGGTGATTTACTATT | 64326 |
rs140171609 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175991796 | CAGGGTCAGGATAAT[C/T]AATATCACTGTTTTC | 64326 |
rs140183724 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175969429 | ACTCTCATTCCAGAG[G/T]TGCCTATCCTTACCT | 64326 |
rs140196232 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175966656 | AGAAAGAAGAAAGGT[A/G]TCTTGGGTGGTCACT | 64326 |
rs140200542 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | RFWD2 | GRCh38.p7 | 1:176115945 | TTCCATGGAAAAGCT[G/T]TTAAGTTTCAACGTA | 64326 |
rs140211835 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176014400 | AGTTATGCTGCCTAG[C/T]TGCAACCTTTATCTC | 64326 |
rs140218836 | snp | A/G | 1.65531e-05 | 0.00287686 | synonymous-codon | RFWD2 | GRCh38.p7 | 1:176046261 | AGTGTCATATTCATA[A/G]ACTTTAATCTTCTTT | 64326 |
rs140230954 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176082164 | CTGTGTCGTTTGAAC[A/G]TATACTTTCCTTTCT | 64326 |
rs140234231 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | RFWD2 | GRCh38.p7 | 1:176076042 | TAGGGGACTTCAATA[A/C]CCCACTCACACCATT | 64326 |
rs140236574 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176178021 | ATGTTCCAAAAACAG[C/T]ATCATCACCTCTTGC | 64326 |
rs140238539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176111181 | ATAATAATAACAGTA[C/T]TTATCTCACAGAGTA | 64326 |
rs140240406 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RFWD2 | GRCh38.p7 | 1:176073358 | ACAGTTTGAACAAAC[A/G]TAAGTAAAAATATTG | 64326 |
rs140258777 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RFWD2 | GRCh38.p7 | 1:176059576 | CAACCTCTGCCTCCT[A/G]GGTTCAAGTGATTCT | 64326 |
rs140271044 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | RFWD2 | GRCh38.p7 | 1:176175580 | GAGACAGAGCACAGG[C/T]AGTAGTGCTCGCTCA | 64326 |
rs140273151 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176107660 | TTAACAATTATTATT[A/G]TAAGTAAGATACAAT | 64326 |
rs140305433 | in-del | -/AAAC | 0.0217236 | 0.101931 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176177783 | ACAAAATACAAAATA[-/AAAC]AAACAAAAAAATAAA | 64326 |
rs140316286 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RFWD2 | GRCh38.p7 | 1:176091387 | TTCTGAAGTTGTGTA[C/T]TTGAATAATACAATG | 64326 |
rs140322049 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176056666 | ACTATAAAAATATTT[C/T]CTTATTGCCAGGAAG | 64326 |
rs140323280 | snp | C/G | 0.0260105 | 0.111035 | intron-variant | RFWD2 | GRCh38.p7 | 1:175994035 | AGCCCATCAGACTAA[C/G]AGGGGATCTCTGGGC | 64326 |
rs140358075 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176178594 | CAGTGGCTCACACCT[C/G]TAATTCCAGCACTAT | 64326 |
rs140363281 | snp | G/T | 0.0228947 | 0.104514 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207371 | CGCGCCCTCGGGGTC[G/T]GGGCTCCCTGGCGAA | 64326 |
rs140383016 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175994990 | AATTGACCACATAGT[G/T]GGAAGTAAAGCTCTC | 64326 |
rs140386767 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175970553 | GCAGTTAAGAAGTAG[A/T]TATAGGAACGACATT | 64326 |
rs140413911 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176027941 | ACTCACAGTTCCACA[C/T]GGCTGAGGAGGACTC | 64326 |
rs140428650 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175979765 | TTCTTAAATGGTAAT[A/T]GATTATTACCATTTA | 64326 |
rs140429326 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176158969 | ATACAGATGAAGTAG[C/T]ATAATATTACTTTAA | 64326 |
rs140435063 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | RFWD2 | GRCh38.p7 | 1:176088231 | CACATTGTGCACATG[C/T]ACCCTAGAACTTAAA | 64326 |
rs140440620 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176122581 | TCTTCAAACAACAGA[C/T]GCTATCACAGTGTTT | 64326 |
rs140453998 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176001977 | TAACATTAATCTTAA[G/T]GAGGATCCCTGGTAC | 64326 |
rs140454098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175968813 | CAAAGTCTTCTCGCC[A/G]ACTGGCCCTAAACAA | 64326 |
rs140460324 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176061107 | GTACTGGCCTAAGAG[C/G]AGACATACAGATCAA | 64326 |
rs140467032 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175999467 | AATGGCTGAATAGTA[C/G]TCCATTTTGTATATG | 64326 |
rs140497651 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:176194032 | CTACAAATGGAAATA[C/T]ACTATTGCAAAATTT | 64326 |
rs140511607 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176190836 | AAATGCTAACTCCAT[C/T]ATGCTTTCATAAAAT | 64326 |
rs140513081 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176164438 | CACCCCAACCCCATG[G/T]ATTACTTTGACTAAC | 64326 |
rs140526877 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176092871 | TCTAGGGAAACTCTT[C/G]CACCTGTGGATCTGG | 64326 |
rs140532089 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | RFWD2 | GRCh38.p7 | 1:175984555 | TCACACAGAGTCCCT[A/G]CTGGGGCACCACCTA | 64326 |
rs140539366 | in-del | -/ACTA | 0.00993419 | 0.0697739 | intron-variant | RFWD2 | GRCh38.p7 | 1:176135715 | CTTCCTTTTTTATGT[-/ACTA]ACTTTGATTAATGAA | 64326 |
rs140546396 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:176127504 | TCATCTAGGTTCATC[C/T]GTGTTGGTGCAAATG | 64326 |
rs140550751 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176065042 | ATATAACTAAGATTA[C/T]AGAAGTTGTACGTAA | 64326 |
rs140559719 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | RFWD2 | GRCh38.p7 | 1:176075771 | GTAGTTTGGGAGGCC[A/G]AGGCAGGTGGATCAA | 64326 |
rs140590774 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | RFWD2 | GRCh38.p7 | 1:176013679 | ACAGAATTTTAACTG[A/C]AGTATGAGAAAATGT | 64326 |
rs140597215 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175992814 | GGCTCCACCTCTGGG[A/G]GCAGGCACAGACAAA | 64326 |
rs140606695 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175954091 | GCTAAAATCATACAA[A/G]TATGTTCTCTGAAGA | 64326 |
rs140626423 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176090089 | CAACCCCTTATCTTA[A/G]CCCAGACACTCCTTC | 64326 |
rs140652009 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176195640 | ACAAAGTTGAATTAT[A/G]TCACAAATCAGACAT | 64326 |
rs140657612 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | RFWD2 | GRCh38.p7 | 1:176082962 | AGGGTCCACTTAGTT[A/G]TGCTTCCATTCTAAA | 64326 |
rs140672817 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | RFWD2 | GRCh38.p7 | 1:176044212 | GATCCAGTTGTGCCA[A/G]ATCATATAAGCCAAA | 64326 |
rs140685022 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175987589 | TTTCTCAGTATAGGA[A/G]TTATTCTATTAATGG | 64326 |
rs140705252 | in-del | -/G | | | intron-variant, downstream-variant-500B, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175968388 | GTATTTAGAGTGGCA[-/G]GTTTTAAAGGCTGTA | 64326 |
rs140709396 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:175956791 | TTAACAAAAAAAGTT[A/C]CTGTAAAATAGGCTC | 64326 |
rs140718222 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176103406 | TCCTAAACAATAAGA[C/T]TGAATGAGTTTCCAG | 64326 |
rs140719455 | in-del | -/TA | 0.0263992 | 0.111815 | intron-variant | RFWD2 | GRCh38.p7 | 1:176200605 | TCACCTACTGCATTC[-/TA]TGTTTCACTTTATAT | 64326 |
rs140727107 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176143903 | GGAGACTACTCAACC[C/T]CACTCAGAAATTTTT | 64326 |
rs140730163 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176018137 | TTAAAGATGCACTAA[C/T]GTTAGCTATTATTAT | 64326 |
rs140735391 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176077173 | AGAGACACAATGATA[A/C]AAGAAAACTTTGGGC | 64326 |
rs140747937 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176172799 | GATCGACATATCTCA[A/G]TGACATTACTCTGAG | 64326 |
rs140748199 | snp | C/T | 0.021333 | 0.101051 | intron-variant | RFWD2 | GRCh38.p7 | 1:175952234 | TGAGAGCAGCCTGGC[C/T]AACATGGTGAAACCC | 64326 |
rs140748641 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:176046432 | TAAATACCTTCAAAT[C/T]GTACTAGACCTCATA | 64326 |
rs140755121 | snp | A/G | 0.155634 | 0.231506 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176206774 | CGGCGGGCGCCACCA[A/G]CACAGGCCGCACCGG | 64326 |
rs140759939 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:175988896 | ACAGATAAATGACCA[C/T]GTCAGTGTAAAAGCC | 64326 |
rs140783121 | in-del | -/CTAT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176180762 | AGAAAAAAGAATAAA[-/CTAT]AACAAGAACAGCCAG | 64326 |
rs140791615 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RFWD2 | GRCh38.p7 | 1:176041540 | TTTTAGTAGAGACAG[A/G]GTTTCACCACATTGG | 64326 |
rs140793678 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176113652 | TTAAAAAAACACCTG[C/T]AGTTAAATAAATTTT | 64326 |
rs140802601 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176145270 | ACCTCATAAGTCATC[A/T]GGAAAATGCAAATTA | 64326 |
rs140814900 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176078191 | TGAATGGCCAAAGCA[C/G]TCCTAAGCAAAATGA | 64326 |
rs140843117 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176139574 | GCCCATCATTGCCCA[C/T]CAACGGTGGACTCAA | 64326 |
rs140859242 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176075288 | GTTAAACAGCTGACA[A/G]AATACAATAAAAGAT | 64326 |
rs140863803 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176147539 | AAGTATTTGGAACTA[A/G]TATGTTTCTTGGTTA | 64326 |
rs140866420 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | RFWD2 | GRCh38.p7 | 1:176180979 | CGAAATAGTAAATCA[A/G]GGCTTGGTAGACATA | 64326 |
rs140872196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175964796 | TTAAATATCCTTCCT[C/T]AAGTAAATATAAAGA | 64326 |
rs140876557 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176141686 | GTTCCTGAAATGGCA[A/G]ACCTGATTAAAAGAC | 64326 |
rs140883361 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175973843 | ACAAACAGAAGTGCA[G/T]GAAAGGGTATTTGGG | 64326 |
rs140883474 | snp | C/T | 1.64784e-05 | 0.00287035 | synonymous-codon | RFWD2 | GRCh38.p7 | 1:176081196 | ATCACTAGCATATGA[C/T]AATGTGGCTAAAGGT | 64326 |
rs140900335 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176057367 | CCCTCTCTTTCCACG[A/G]TCTCCCTCTGATGCC | 64326 |
rs140911635 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176176843 | CAAAAGAAAATAATG[A/T]CATAGTTAAAGAGTA | 64326 |
rs140915105 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175992824 | CTGGGGGCAGGCACA[A/G]ACAAAAAGACAGCAG | 64326 |
rs140920866 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176174547 | TATGTAATCCTCCAG[C/T]GATTTTCCTTCATAA | 64326 |
rs140931668 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176076130 | CCAACTGGATACACA[C/T]TGACACAGAGTACTA | 64326 |
rs140972145 | snp | A/C | 0.39009 | 0.207062 | intron-variant | RFWD2 | GRCh38.p7 | 1:176005013 | GGTAAGCTATTGATT[A/C]TTGCCACAATTTCAG | 64326 |
rs140993751 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176178225 | ACATGAAGAAATTTA[C/T]AGTCTGCTTAGGGAA | 64326 |
rs141010653 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175999671 | CTCTAGTTTTAATTT[C/T]TTAGGAATCTCCAAA | 64326 |
rs141022836 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176009434 | ACTAACGTATTCTCA[C/T]GTTAATACAAAAGGG | 64326 |
rs141026995 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175951814 | TCAGTGACCTATTGG[A/G]CAATATGCAACCTAA | 64326 |
rs141056672 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176045136 | CAGGTTATTTACCTT[C/T]CTGTGCTCAGCTTTC | 64326 |
rs141069591 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176198126 | CCTACATCCTTTTTT[A/G]TAGAAATTGGCACGC | 64326 |
rs141098732 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176169527 | TGAATTTTGGTTTCC[C/T]AATATACATAAAAGT | 64326 |
rs141142668 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | RFWD2 | GRCh38.p7 | 1:176125002 | GTAGTTGTGATTTGC[A/G]TTTCTGATGATCAAT | 64326 |
rs141149413 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176040149 | AGAACACTATAAAAA[A/C]ACTAAAATAAATATA | 64326 |
rs141157200 | snp | C/G | 0.0228947 | 0.104514 | intron-variant | RFWD2 | GRCh38.p7 | 1:175995286 | TAAATGCTCACAAGA[C/G]AAAGCAGGAAAGATC | 64326 |
rs141157504 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176035174 | TTTAAAGCAACTATT[A/G]TAATTATACTCCATG | 64326 |
rs141173354 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176032661 | TGGGCTTGTGACAAC[A/G]CAGATGTTTCTCCCA | 64326 |
rs141197532 | in-del | -/CTCC | 0.401747 | 0.198678 | intron-variant | RFWD2 | GRCh38.p7 | 1:175986553 | GTACCAATTCTTTTT[-/CTCC]CTCCCTATTAAAATA | 64326 |
rs141211507 | in-del | -/A | 0.00636936 | 0.0560724 | intron-variant | RFWD2 | GRCh38.p7 | 1:176171687 | AACTTTCAATTTGTT[-/A]AAAAAAAATGCAACT | 64326 |
rs141216757 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176089331 | ACAACAACAACAATC[A/T]ATTTAATACTGATTA | 64326 |
rs141226299 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | RFWD2 | GRCh38.p7 | 1:175950035 | GAGGAGTTTAAAATA[G/T]GTACAATTACCACTC | 64326 |
rs141230404 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | RFWD2 | GRCh38.p7 | 1:176126213 | GATGCTCTTTATTTC[C/T]TTCTCTTGTCTGACT | 64326 |
rs141245057 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176130064 | CATTTGTTAATCCAT[A/G]TAACGTCCACCCAGT | 64326 |
rs141250395 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:176065970 | TCCTGACCTCAAACA[C/T]CTGCCTCGGCCTCCC | 64326 |
rs141262611 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176076298 | CACAGTGAATAAACA[C/T]AGAAATCAATATCAA | 64326 |
rs141284208 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176123301 | TCGGTAGGAGAGATG[C/T]CATGAACAGCAGAAA | 64326 |
rs141284484 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176170256 | CTCCCATGAAACATG[A/T]GTGTTCTTAATGGCA | 64326 |
rs141287354 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176018625 | GATTCTGTTTATCAA[C/T]AGGGAAAAAATAATT | 64326 |
rs141287516 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176057105 | AGACAAACTACCCCT[A/G]CGTTTCCAATATTTG | 64326 |
rs141290680 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | RFWD2 | GRCh38.p7 | 1:176141935 | GACAAAGTCTCACTA[C/T]ATTGTCCAGGCTGGT | 64326 |
rs141293850 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175960465 | AATTGCTTCTGGCTT[A/T]GCAGTTCAAGGAAGG | 64326 |
rs141342495 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176165028 | CTGATACTTCCCAGT[A/G]TATCACAATGCAAGT | 64326 |
rs141352196 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | RFWD2 | GRCh38.p7 | 1:176054898 | CCTCTCCTCTCGTTC[C/T]CTTTAACTCACTGGA | 64326 |
rs141388534 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175990389 | TAAATTTATTGACTT[A/T]TTTTTAGTCTTAAAT | 64326 |
rs141406666 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | RFWD2 | GRCh38.p7 | 1:175988473 | CACGAAACTCATCAC[C/T]ACTAATTAGAGGCAA | 64326 |
rs141409649 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176155313 | CTCATCCTTGCTCCT[A/G]AAAACTAAAATAAAT | 64326 |
rs141417272 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | RFWD2 | GRCh38.p7 | 1:176079951 | CTGCATGAGCCTAGG[A/C]GTCTGAGGATCGCCT | 64326 |
rs141438109 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176173850 | AAAATTAGCCGGGTA[C/T]AGTGGCGCACGTCTG | 64326 |
rs141445267 | snp | A/G | 0.00398564 | 0.0444627 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176208104 | ATTTAATACCACCAG[A/G]AAATATACAATTTCT | 64326 |
rs141447618 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176183282 | CTTCAGCATAAAATT[A/G]CGGGCCTGATTTCAA | 64326 |
rs141473586 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:175984802 | AAAGGAGATCATTTT[A/G]GAACTTTAAGATTTG | 64326 |
rs141486618 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:175980931 | GTCCCTTTACACAGG[C/T]ATCATCACATAGGAA | 64326 |
rs141491498 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant, utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175971711 | GGCTGTAAACATCAG[A/T]ACACAGTACCTTTCA | 64326 |
rs141528326 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176025322 | GAAGAAATGCAATTA[C/T]TGCTTTGGGCAGATA | 64326 |
rs141531591 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176152708 | GGCCTCCCAAAGTGC[C/T]GTAATTACGGCGTGA | 64326 |
rs141550890 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176010054 | ATCCAGTCTGCAAAG[A/C]AGCTGAAAGAACAGC | 64326 |
rs141552523 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:175978295 | TCTATTACAGAAATA[A/T]AAAAATGATAATAAT | 64326 |
rs141558634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176119816 | TTACTATGCACTAAC[C/T]TAAATAATTTAAACT | 64326 |
rs141561647 | snp | C/T | 0.16618 | 0.23553 | intron-variant | RFWD2 | GRCh38.p7 | 1:176058418 | TTTCATTTTGCTCTG[C/T]ACTAAGAAAAATTCT | 64326 |
rs141597257 | snp | A/G | 0.00237212 | 0.0343574 | missense, intron-variant | RFWD2 | GRCh38.p7 | 1:176149043 | ACCTTGAGGAATTCC[A/G]TAAGAATCTGTAGTT | 64326 |
rs141603606 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | RFWD2 | GRCh38.p7 | 1:176006639 | ATATGAAATTCTGGG[C/T]TGAAAATTCTTTTCT | 64326 |
rs141607792 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176069058 | CCAGGCGTGGTGGCA[C/T]GTGCTTGTAGTCCTA | 64326 |
rs141617800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176162714 | AAGTTACAAAAAGGG[A/G]GAATCTAGCAGAAGT | 64326 |
rs141627688 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176068115 | TACTGTGAACCTAAA[A/C]CTGCTCCATAAAATA | 64326 |
rs141667133 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176062875 | AAAAACAAGCTGGGC[A/G]AAATAAGCTAGACAC | 64326 |
rs141692691 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176165825 | GCCAGATTGTGAAGG[G/T]CCTGAACTGCAGATA | 64326 |
rs141696579 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:175947649 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGTGCC | 64326 |
rs141702443 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RFWD2 | GRCh38.p7 | 1:176042195 | AGAATCACTTGAACC[C/T]GGGAGGTGGAGGTTG | 64326 |
rs141704560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176002273 | TTTCTTTTATTCTTT[C/T]TTCTTTGTATTCTTT | 64326 |
rs141713739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175953275 | GTAAAGGAGAAAAAA[C/T]ATTATAAAAATACTC | 64326 |
rs141725696 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | RFWD2 | GRCh38.p7 | 1:176103585 | CCAAAATGCTCCAAT[G/T]AGCATTTCTTTTGAG | 64326 |
rs141727637 | snp | A/C/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176095811 | AACAGCACCAAATCC[A/C/G]ACTGGTAGACACTGT | 64326 |
rs141734461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176010110 | TTCTAGACTCACCAA[C/T]TGTAAATGTTTCACC | 64326 |
rs141735455 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176108552 | TCAACTACCACTCTC[C/T]CTTCCTCCACCTACC | 64326 |
rs141749972 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176102472 | GCCACTGCAAAATTA[C/T]AGCTAAGACAGTGAA | 64326 |
rs141751545 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176199930 | CAAATTATAACTTAG[C/T]AAAGCTAATTTTAAA | 64326 |
rs141758186 | snp | A/T | 0.0189856 | 0.0955633 | intron-variant | RFWD2 | GRCh38.p7 | 1:176099488 | ACACTCCTGTGAAAA[A/T]AATTTGGAGCATATT | 64326 |
rs141768469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176039423 | AAGTTAAATCTAAAG[C/T]AAGCAGGGAAAAAAA | 64326 |
rs141806740 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176138711 | AATTAGTTTTCCACC[A/G]TAACATAAAAACCAC | 64326 |
rs141817315 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175958905 | AAGAAAGAAATAATT[C/T]CGTATTACACAAATT | 64326 |
rs141826235 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176135678 | CATTATATAAATTTT[A/C]TCTCTCACACTGACA | 64326 |
rs141843603 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176052863 | CTCATGCCATAGTAT[C/T]TTGACCATCATTTCA | 64326 |
rs141858031 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176203826 | AGTCAGGAGAGGCCA[A/G]TGTTTATTACTGAAA | 64326 |
rs141861077 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:176139392 | AGCCACTGTGGAGAC[C/T]GGAGTTGGGAGATTT | 64326 |
rs141866461 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176200244 | TTTGAGCACTTATTA[C/T]TATGAGTATTTGTCC | 64326 |
rs141875065 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176153635 | ATGTTGAATAAACAG[A/G]AGTAGTGAAAGAGGG | 64326 |
rs141880067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175969062 | TTCGCAAATTTCCTC[C/T]AGACTACTCTGGTAA | 64326 |
rs141915250 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:175965392 | TTAAGTGATACTATT[C/T]AATTGTCCAATTTCA | 64326 |
rs141929602 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175963552 | TTTTAAAGGAACTCA[A/G]GCATATATGCCTTAA | 64326 |
rs141939284 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | RFWD2 | GRCh38.p7 | 1:176198867 | AAATATGTTACATAA[A/C]AATGTGATAAAACTA | 64326 |
rs141942987 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176132550 | ATGAATATATACACA[C/T]ATATACACATATGTA | 64326 |
rs141949225 | in-del | -/T | 0.093777 | 0.195178 | intron-variant | RFWD2 | GRCh38.p7 | 1:176079685 | AAAAAATAAAAGTGG[-/T]TCAGGGAACATGGAA | 64326 |
rs141964397 | in-del | -/CAGGCT | 0.0693013 | 0.172766 | intron-variant | RFWD2 | GRCh38.p7 | 1:176096346 | CCACTTAAATGGCCA[-/CAGGCT]CAGGCTCAGGCTCAG | 64326 |
rs141980763 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | RFWD2 | GRCh38.p7 | 1:175995819 | ATTCTACCAGAGGTA[C/G]AAGGAGGAACTGGTA | 64326 |
rs141988457 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176087743 | CATTTGACTCAGCCA[A/C]CCCATTACGGGTTAT | 64326 |
rs142011965 | snp | C/T | 0.00953873 | 0.0683987 | downstream-variant-500B | RFWD2 | GRCh38.p7 | 1:175944328 | AACCGAAAATATATC[C/T]GGCCCTTTACAGAAA | 64326 |
rs142019415 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176192792 | CATTAGATAGTATCC[C/T]CATCCCATTATTCAG | 64326 |
rs142022299 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176029355 | GCAAAGCTGACTAAG[A/C]AAAATAGGTCTGATT | 64326 |
rs142046153 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:175960015 | TTTAAGTGGCAAGCC[A/G]AATTTGATATTCAAT | 64326 |
rs142057058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175991631 | TTTTGACTCTTGTAA[C/T]AACACTTAGCTTAAA | 64326 |
rs142064140 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176021839 | TATTGAAAAAGAGAA[A/G]CATAAAAAATCATTT | 64326 |
rs142067088 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176055266 | CGATGAAATCCAGCC[C/T]CTACCAAAAATACAA | 64326 |
rs142082939 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176098786 | TCAAGTGTTTTAAAC[C/T]TCTAACATATTTAAC | 64326 |
rs142086947 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176082052 | ATAGTATCAGTTTAC[A/G]AAGTACCTGAGAATA | 64326 |
rs142093138 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176117000 | AAGGTTTGGAGAACT[G/T]TAAGGAAAAGAAAAT | 64326 |
rs142100060 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176034651 | GAAAGTAATGGAGAA[A/G]GAGATTCTACAGTTC | 64326 |
rs142102569 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | RFWD2 | GRCh38.p7 | 1:176054458 | TGACCCACTGCACCC[A/G]GCCAAATTACTCTGT | 64326 |
rs142111001 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:175993474 | AAACTTAAACCAAAG[A/G]CAAAGAAGTTGAAAA | 64326 |
rs142111295 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176185723 | GAGGATACTGGTTCC[C/T]GGATGAAATCCTTGA | 64326 |
rs142127163 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992092 | TTTTTAATTTTTTTT[A/G]AGTATTATAGTTGGT | 64326 |
rs142130928 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | RFWD2 | GRCh38.p7 | 1:175972805 | CAGGAAGCTTTTTAG[C/T]TCATTGAGAATAACT | 64326 |
rs142130934 | snp | A/C | 0.000263957 | 0.0114852 | missense | RFWD2 | GRCh38.p7 | 1:176043810 | TGGTAACTACTCCAA[A/C]TGATACAGCTGAAAG | 64326 |
rs142132211 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176053288 | CCTGGAAGTAAATTC[A/G]GTGTGCTTACTATAC | 64326 |
rs142136175 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176087479 | CAAAAGAAGACATTT[A/C]TGCAGCCAACAGACA | 64326 |
rs142165867 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176086874 | TACTACAAGGCTACA[G/T]TAACCAAAACAGCAT | 64326 |
rs142185557 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176153782 | TACCTAGTTTATTGA[A/G]AGTTTTTAATATGAA | 64326 |
rs142188352 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176022898 | TAGATTCCATCAATC[A/G]GATGCACTTATTTAA | 64326 |
rs142193138 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176121823 | GACAATGGCTTTTTA[A/G]CAATATGTAGATTTT | 64326 |
rs142197782 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176189002 | TAAAATAACAAAATA[A/C]ATCAAACCACAGATC | 64326 |
rs142200350 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176060003 | TTAATAGCAACCTGC[C/T]AGATAATTGCTGACC | 64326 |
rs142226935 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176164178 | TTGCTGAGAGAGAAA[A/T]CCTCATTCACCATGT | 64326 |
rs142236048 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175979570 | AGAACATAATATAAA[C/T]GTAATAAAAATATTA | 64326 |
rs142237260 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176186779 | GAAACAGTGTTGAAA[C/T]GGACTAGGGTGGTAG | 64326 |
rs142243391 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176118954 | AGAAATAAAGTTAGA[C/T]GAGTGCCAAAAAATG | 64326 |
rs142263405 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176070862 | CTTGCTATGCTTCCC[A/G]GGCTGGTTTTGAACT | 64326 |
rs142269519 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | RFWD2 | GRCh38.p7 | 1:176008689 | ATGTGGCAACTGTGG[A/T]CTCGGTTCTTCCTCC | 64326 |
rs142299320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176105352 | AAAGAAATATCACAA[C/T]GAAAATTGAAGAAAA | 64326 |
rs142331098 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RFWD2 | GRCh38.p7 | 1:175946687 | CTATCAATTTTCAAC[C/T]GAACACTAAAATAAC | 64326 |
rs142337999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176114588 | TAATTCTTTTTTTTG[C/T]GGGGGGAGGGAGTGG | 64326 |
rs142355944 | in-del | -/TG | 0.0685596 | 0.171987 | intron-variant | RFWD2 | GRCh38.p7 | 1:175959947 | CCCTTTATCTTGTTT[-/TG]TGTTTCAGGTTTAAC | 64326 |
rs142361578 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | RFWD2 | GRCh38.p7 | 1:176099110 | ACTTTGTCAATTGTG[C/T]TTCTAACTGTAACTA | 64326 |
rs142378466 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:175985693 | TCTGGTAATTCTTTC[C/T]TGTCTTGTTTGCTTT | 64326 |
rs142378575 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | RFWD2 | GRCh38.p7 | 1:175944785 | ATGCTACTTCTTAAA[A/C]AGAGTTATCTCTTGC | 64326 |
rs142398548 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176013279 | TCATCCCAAAAATAT[A/T]TGATTATAGTAAGAA | 64326 |
rs142414026 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:175966209 | AAACTAAAATGTTAG[C/T]TAGCCTTCCCTGCAT | 64326 |
rs142419150 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176201148 | TTTCAGATTAAGGAT[A/G]CTAACCTGGTAAATA | 64326 |
rs142428186 | in-del | -/TC | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176010167 | ACACACCGCCTCTTG[-/TC]TCTCTCTCTCTCTGC | 64326 |
rs142429240 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | RFWD2 | GRCh38.p7 | 1:176110019 | GCGGTATTTTTTGAG[C/T]GCACTGATTTTTTAA | 64326 |
rs142436396 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176150432 | ACTGACTTTGACTGG[A/T]CCTTAGACCCATTCT | 64326 |
rs142476652 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176039164 | TTAAACTAGAAATCA[A/G]TAACAGAAAAATAGC | 64326 |
rs142484586 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175980174 | GGTCACACAGCTGAT[A/C]AGTGGGGAATCTGAG | 64326 |
rs142488015 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | RFWD2 | GRCh38.p7 | 1:176040639 | TCAAGGAAAAAAGGT[A/G]TTCCATTCTGTATAT | 64326 |
rs142488834 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176072310 | CAGCAGGTAAAACAA[A/G]TTTTCATTCATTCAT | 64326 |
rs142489034 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:176036778 | AATTGTAGGCCAATG[C/T]AAATATTCTGAGCAC | 64326 |
rs142494413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176206356 | TTACCTACCTCTTTA[C/T]TATCCCCACCCTGCC | 64326 |
rs142495867 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:175982168 | AGCAATTACACTTCT[A/G]AGCATTGAATCCCAC | 64326 |
rs142497295 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | RFWD2 | GRCh38.p7 | 1:175976811 | AATATTTAGATAGCT[C/T]GTAATGAAATAAGAC | 64326 |
rs142498181 | in-del | -/A | 0.108048 | 0.20579 | intron-variant | RFWD2 | GRCh38.p7 | 1:176154459 | ATGCTATGCAGCCAT[-/A]AAAAAAGGAGATCAC | 64326 |
rs142503155 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | RFWD2 | GRCh38.p7 | 1:176017629 | TCCTGGGTTCAAGCT[A/G]TTGTCATGCCTCAGC | 64326 |
rs142508386 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175959719 | ATAGATAATATACAC[A/C/T]TGTGGTAAAAATTCA | 64326 |
rs142519472 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175969734 | CCAACAGGTGAGAAA[A/T]ATCTTTTCTCCCTTA | 64326 |
rs142537640 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176154507 | AAATGAAGCCAGAAA[C/G]CATTATCCTTAGCAA | 64326 |
rs142540971 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176132207 | CACACAGGGATCCAA[A/G]TAAACATTTTAAAAT | 64326 |
rs142544251 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RFWD2 | GRCh38.p7 | 1:176137967 | CCAATAGTTGAAATA[C/T]CATAGCAAGCATTAT | 64326 |
rs142552159 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | RFWD2 | GRCh38.p7 | 1:176067572 | AGCGGCCCGACTCCA[C/G]GGGAAACCCACTTTC | 64326 |
rs142555068 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176074165 | CTCCTGGCCTCAAGT[A/G]ATCTGCCTGCCTCGG | 64326 |
rs142556651 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176037706 | ACTACATGATGATAC[A/G]TGCATAAAAAGTATT | 64326 |
rs142567932 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176069675 | AAGCTCTTTAAGGAC[C/T]CTTTGACACCTTGCC | 64326 |
rs142572830 | in-del | -/C | 0.116138 | 0.211142 | intron-variant | RFWD2 | GRCh38.p7 | 1:176143956 | GGTAAAAATTTACTA[-/C]CTTGAGTGATAAAAA | 64326 |
rs142578488 | snp | C/T | 0.021333 | 0.101051 | intron-variant | RFWD2 | GRCh38.p7 | 1:176001240 | TTAACATCAGAATTG[C/T]CTGAATCATCAGAAA | 64326 |
rs142600567 | snp | A/C/T | 0.00597694 | 0.0544006 | intron-variant | RFWD2 | GRCh38.p7 | 1:176171909 | TGAATAAAAAGCTTA[A/C/T]TTATATATTTTTAAA | 64326 |
rs142614895 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176175683 | CAGGGGTCCCTGATA[C/T]ACACAATAATCTAAA | 64326 |
rs142639388 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176057122 | GTTTCCAATATTTGC[G/T]GAACATTCCAAACTT | 64326 |
rs142645935 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176159882 | ATGAAAATAATTACT[A/T]CTTAAGTCAGATCTA | 64326 |
rs142685717 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176170555 | TTTTCTAAGCAGTAG[A/G]TCTCAACAGTGGTCT | 64326 |
rs142691375 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176062101 | GCCTTTCCAGGTTCA[A/C]GTCATTCTCCTGCCT | 64326 |
rs142697904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176000868 | TTTTTTCTGGGGATT[A/G]TAATTGGCATGTTAA | 64326 |
rs142701216 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | RFWD2 | GRCh38.p7 | 1:176095297 | GTGGTTATCATAGTG[C/T]GATCCCCAAAATGTG | 64326 |
rs142706759 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175945813 | CACTACAACACTCAC[C/T]AAGTAGCAAATATTT | 64326 |
rs142710089 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176194720 | ACAAGAAACCCACTT[C/T]AAATATTAAAACACG | 64326 |
rs142731221 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176163220 | CAAATATAAAAGGTG[C/T]CTTTGAGACTATTCT | 64326 |
rs142731377 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176199578 | TATATCCATATAATG[A/G]GATAATACTAAGCAA | 64326 |
rs142731930 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176091521 | TATGGGGCTTAAGAA[C/T]AAGACAAAAAATTAT | 64326 |
rs142750700 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175964425 | GAAAATTTTACTGGG[A/G]AAAAAAAGCCCAGAA | 64326 |
rs142764439 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:176196642 | ATATGAAGACCCAAA[A/C]CTATGGCTTCACCAG | 64326 |
rs142773082 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176101416 | TTTGGAAAAAAAAAG[C/G]CTTTCTTTTTCCTTT | 64326 |
rs142779909 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176028634 | TGTAACACAGACCCA[A/C]AACTAAGACATAAAA | 64326 |
rs142786755 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176041246 | TCTAAATGTCTCCAT[A/G]TGGAATGAATCTAAA | 64326 |
rs142865467 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | RFWD2 | GRCh38.p7 | 1:176112184 | CAAACCAAAAGTCTC[C/T]TTCACCACATAAAAG | 64326 |
rs142867398 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | RFWD2 | GRCh38.p7 | 1:175958439 | AAATAAGGCACTGAA[C/T]TATCAAAAAGAAAGG | 64326 |
rs142876048 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176197685 | CAAATAAATCCATTA[A/T]CGTACGTTCTTTAAA | 64326 |
rs142878506 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176131853 | TTCACATCACTTGTT[C/T]AGAGAAAATATCAAA | 64326 |
rs142883060 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | RFWD2 | GRCh38.p7 | 1:176024041 | GGCAGGCAGATCACT[G/T]GAGGTCAGGAGTTCG | 64326 |
rs142887536 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:175951207 | TGAGCCAAGATCATG[C/T]CACTGCACTACAGCC | 64326 |
rs142893950 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175965738 | GGATTACATGTGCGT[A/G]CCACCAAACCCAGCT | 64326 |
rs142916625 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176044824 | ATTTATTCCAATATA[C/T]CAGGAAGTATTGCAC | 64326 |
rs142920790 | snp | A/G | 0.0018643 | 0.0304742 | synonymous-codon | RFWD2 | GRCh38.p7 | 1:175988318 | CTCCATTGGAAGCCA[A/G]GCCTACAAAGTTTTT | 64326 |
rs142925110 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176052777 | TAAACACGCATACAC[A/G]TATTTGGTTTTTTTC | 64326 |
rs142925366 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:176011201 | TCCAGTACAGTAGTC[A/T]CTAGCCACATGTGGT | 64326 |
rs142933471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175954203 | AAATAACCCAGGGAT[A/G]GAAATGAGAAACCAT | 64326 |
rs142938634 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:176119700 | AGCACTGACAGGGCT[C/G]GGTCCCTCTTGACTC | 64326 |
rs142941928 | in-del | -/AAGGTCTCA | 0.309401 | 0.24284 | intron-variant | RFWD2 | GRCh38.p7 | 1:175976065 | AAGATGTAGAATTAG[-/AAGGTCTCA]AAGGTCTCAATCCTT | 64326 |
rs142942753 | in-del | -/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176096679 | TTTTACGTGAGAGGA[-/T]TTTTTTTTTCCTTTT | 64326 |
rs142946160 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176144678 | ACAAGGTGGTATTGC[A/G]AAAAAGACCAGTGAA | 64326 |
rs142948527 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176077786 | GGCTCCTGGAACTGA[C/T]AGACAAATTCAGCAA | 64326 |
rs142951234 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | RFWD2 | GRCh38.p7 | 1:176179763 | AAAATTTTTTGTCAA[A/T]ATACAAGAAATTATT | 64326 |
rs142966098 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | RFWD2 | GRCh38.p7 | 1:176055788 | CTCATGAATTGATTT[A/C]GTAATTGTTTTTTCA | 64326 |
rs143003575 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | RFWD2 | GRCh38.p7 | 1:176115764 | ATAAAATAAAATAAA[A/G]TATAAAAATAAAAAG | 64326 |
rs143003682 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:176161559 | GCTATGACTGTACCA[C/T]TGCACTCCAGACTGG | 64326 |
rs143017955 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176158179 | AAACTGGGAGAAACA[C/T]ATTTCATTAAGAAGA | 64326 |
rs143042078 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176175146 | TCCCAACTCAGCAAG[C/T]ATCACACCCAAGTTT | 64326 |
rs143056959 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | RFWD2 | GRCh38.p7 | 1:176148029 | ATTTATATTGCACCA[C/G]CAGACATTTAAACAA | 64326 |
rs143062644 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | RFWD2 | GRCh38.p7 | 1:175985748 | TTTTAAAAATACATA[C/T]ATTTGGTCCTTTTTT | 64326 |
rs143069314 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176144093 | TATTCATCATTGTAC[C/T]GGATGTCCTAGCCAG | 64326 |
rs143089393 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | RFWD2 | GRCh38.p7 | 1:176076144 | ATTGACACAGAGTAC[C/T]ACACCCAACAACCAC | 64326 |
rs143112989 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176202502 | CCTCACTTTTTAATA[A/G]TCTGAAAAACAGAGC | 64326 |
rs143120211 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | RFWD2 | GRCh38.p7 | 1:176015638 | GCCTGGTTACAGTAA[C/T]GGCTTGAACTAGAGA | 64326 |
rs143133160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176027292 | TGACCTTATGTTTGT[A/G]AATAAGTAATAAGCA | 64326 |
rs143137160 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175968281 | AAAAACCAGTTCAGA[C/T]GGATACAGAGGTAAC | 64326 |
rs143146276 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:176051085 | ATAAGGTAGCCTCAC[C/T]GGTTTTATAATTAGT | 64326 |
rs143147614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176178272 | CATTACCAGGAAATA[C/T]ACATACAAAATTTAA | 64326 |
rs143151511 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176111878 | GGCCTTCAGTGCAAT[C/G]TATCATGTCAGCTCC | 64326 |
rs143155246 | in-del | -/ACAC | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176188849 | ACACACACACACACA[-/ACAC]CACACACACAGACAG | 64326 |
rs143203043 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176150780 | AATTAACTTGTAGAA[A/G]GAAGGAGAAAGTCCC | 64326 |
rs143233073 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176000484 | AACATGTGAGTAATG[C/T]CTGCACTATGAAGTT | 64326 |
rs143241436 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant, utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175971686 | AATCAGTCAATGTTT[A/T]ATGGAATTTGGCTGT | 64326 |
rs143252022 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176114965 | AAAGAAACATATGTG[G/T]GTACCTTACTCAAAC | 64326 |
rs143254498 | in-del | -/ATAG | 0.0372196 | 0.131242 | intron-variant | RFWD2 | GRCh38.p7 | 1:175962105 | GCCTTTATGCAAAAA[-/ATAG]ATAGGAGCAGTTTTT | 64326 |
rs143257919 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176055240 | GGACTTTGAGACCAG[C/T]CTGGCCAACACGATG | 64326 |
rs143264745 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176145712 | ATGAATCTTAACATT[C/T]AGCCGAAGAAGATAG | 64326 |
rs143269291 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176064843 | TGCCCAGACTGGTCT[C/T]GAGCTCCTGGGCTCA | 64326 |
rs143274090 | snp | A/C | 0.0711525 | 0.174681 | intron-variant | RFWD2 | GRCh38.p7 | 1:176002095 | ATCTACTTGGGGTTT[A/C]TTGAGCTTTTTGGAT | 64326 |
rs143280825 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176006363 | ATTTAAAGTTAATAT[A/T]GTTATGTGTGAATTT | 64326 |
rs143283667 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176156402 | AACAGGAGGGAGAAA[G/T]GGAAAACAAATACCA | 64326 |
rs143285872 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176094207 | AGTAAACTCATTTTC[G/T]CAATTATTTTCCTGT | 64326 |
rs143300534 | in-del | -/ACAATA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176189847 | TGGACTGAAAGAAAT[-/ACAATA]ACAATAATTAAAAAA | 64326 |
rs143381146 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:175948557 | CTTCAGCTAAGCTGA[G/T]TTAAACTTTAGTTTC | 64326 |
rs143383788 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176001821 | GTTTATCTGGGAATA[C/T]CTTAATTCCCCCTTC | 64326 |
rs143389697 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176162134 | AAATCCCTATCTCAT[A/G]TACTTGTAGTCTTCC | 64326 |
rs143391677 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176090936 | AAAAAGAAACCCACA[A/G]TTAGACACACTAAGG | 64326 |
rs143395839 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176196188 | AAAATCAATGATCTA[A/C]GCTTTCGTACTAAGA | 64326 |
rs143397452 | in-del | -/T | 0.00636936 | 0.0560724 | intron-variant | RFWD2 | GRCh38.p7 | 1:176055749 | TAGGTTGACTAACAA[-/T]TTTTCATCTTTTGTT | 64326 |
rs143405319 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176103282 | ACAAAGCCTTAGGAT[A/G]AGGCTGGTCAAAAGA | 64326 |
rs143414053 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176033726 | ATACTTGGAACTAAA[A/T]TATTTTAAAAATATA | 64326 |
rs143447702 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176097161 | GCTTAATTAAAAGTA[C/G]ATATCCAAGTTGTAG | 64326 |
rs143451628 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176038630 | CGAGACCAGCCTGAC[C/T]AATATGGTGAAATGC | 64326 |
rs143455677 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175999357 | AGTGAGAATCCGTGA[C/T]GTTTGTCTTTCTATG | 64326 |
rs143462745 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:176196355 | AAAATTAATAATCCT[A/C]TAGCTAAACCATTCA | 64326 |
rs143463836 | in-del | -/A | 0.498964 | 0.02274 | intron-variant | RFWD2 | GRCh38.p7 | 1:176088996 | CAAAACTCAGTCTCC[-/A]CAAAAAAAAAAAAAA | 64326 |
rs143466936 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176129095 | GCTATTATGCAGTAT[C/T]GTTTCTTAAATATCA | 64326 |
rs143474987 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176193158 | ATAAATGAATGGCCA[A/T]CAAGCTCTTGAAAAG | 64326 |
rs143475763 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:176107495 | CCAACTAGCCAAATA[C/G]AAGATGATTTGAGTT | 64326 |
rs143478937 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176125300 | CTTTGGTTGCCTGTG[A/G]TTGTGGGGTATTACT | 64326 |
rs143483277 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:175952822 | CTCCGGAGGCTGAAG[C/T]GGGAGGATCTCTTGA | 64326 |
rs143521254 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176199826 | TTCTGGAAATGTATC[A/G]TATCTTCATTAGGGT | 64326 |
rs143538451 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176048557 | CCAACTCAATTTATA[C/T]CCATAGTCTCATGTC | 64326 |
rs143547335 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175964523 | TACACTGAAATACTA[C/T]TTACATTTGTCCTCT | 64326 |
rs143549335 | in-del | -/AAC/AACAAC/AACAACAAC | 0.477684 | 0.103247 | intron-variant | RFWD2 | GRCh38.p7 | 1:176089299 | TCTGTCTAAAACAAT[-/AAC/AACAAC/AACAACAAC]AACAACAACAACAAC | 64326 |
rs143564414 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176147138 | CTGTATTTTACTTGA[A/G]TAAGTTCAAGTATAT | 64326 |
rs143565327 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176133243 | ACGTATATGTACGTA[G/T]GTACACACATACGTA | 64326 |
rs143571470 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176079317 | AAAATAATAAAACCA[C/T]GTCCTCTGCAGCAAC | 64326 |
rs143572752 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176035533 | ACAGGGATAGTGATA[C/T]TATATATTAACAAAT | 64326 |
rs143589977 | in-del | -/AAA | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:175981811 | ACAAATAACCCACTT[-/AAA]AAACAAGCAAAGAAC | 64326 |
rs143597516 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176181878 | AAACAAAAAAACACA[C/T]GTTCTCATCAGGGTA | 64326 |
rs143617220 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176197333 | GGAGGAGGATCCCTT[A/G]GGCCCAGAAGTTCGA | 64326 |
rs143633426 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176130939 | TTTCCCTGCCCCTAA[C/T]TTTTTAGGGAAATGG | 64326 |
rs143636485 | in-del | -/TAA | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:175946976 | AAACTGACCATCTAT[-/TAA]TCCATCCAGCATCCA | 64326 |
rs143650797 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175989936 | GTATTTCTGCACTCC[A/G/T]ATAAGATCACTCATT | 64326 |
rs143657447 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175999509 | CCTTATTCATTCATC[C/T]GTTGATGGATACAAA | 64326 |
rs143673533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176083988 | TTGTAAAGCTACACC[C/T]CCAAATATAAACTGA | 64326 |
rs143680715 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176023993 | CCGGGCATGGTAGCT[C/T]ATGCCTGTAATCCAA | 64326 |
rs143683297 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176195433 | ATACAGAAAATGAAT[A/G]GGAGTATACTGAACT | 64326 |
rs143689985 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176036044 | CAAGAGAAATCAAAC[A/G]GAATTTTAAACAGAA | 64326 |
rs143702230 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176079617 | TAACAAACCTGCTTA[C/T]GTACCCTTTAATCTA | 64326 |
rs143704693 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | RFWD2 | GRCh38.p7 | 1:176187924 | AAACATGGGCCTTTG[A/G]GAGATTTTTAGGTCA | 64326 |
rs143706404 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176119306 | TTGCATATTTAGAGG[C/T]CTATAGAACAGAACA | 64326 |
rs143734733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175959212 | TGAAAGAAAAATATT[A/G]TATCATGTTAAATAG | 64326 |
rs143741566 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176004740 | tttttgatgtgctgc[G/T]ggattcgttttgcca | 64326 |
rs143747043 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | RFWD2 | GRCh38.p7 | 1:176093823 | AGCCTAGGTGACAGA[C/G]CGAGAGACTCTGTCT | 64326 |
rs143797386 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | RFWD2 | GRCh38.p7 | 1:176039789 | ATAATTTTTGACAAG[G/T]GTGCCAGACCATTCA | 64326 |
rs143798898 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176050369 | CCGTCAATAAGCCCA[A/G]GCAGTGAATTTTGTC | 64326 |
rs143802717 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175980705 | TTTTGCCTGAGGATA[C/G]AGTGTACTTTTTGGG | 64326 |
rs143810723 | snp | C/G/T | 0.00796298 | 0.0626859 | intron-variant | RFWD2 | GRCh38.p7 | 1:175991096 | TTTCAGATTTTGGAT[C/G/T]TGAGATGCTGAACAG | 64326 |
rs143817353 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176124741 | AACATGGGAATGCAG[A/G]TAACTCTTTCATGTA | 64326 |
rs143817522 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176182884 | AAGAAAGTAAAATGA[C/T]TTAAAAAAATAGTAA | 64326 |
rs143821240 | in-del | -/TC | 0.093417 | 0.194889 | intron-variant | RFWD2 | GRCh38.p7 | 1:175952798 | CATGCATGCCTCTAG[-/TC]CCAGCTACTCCGGAG | 64326 |
rs143824955 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176076628 | TAAAATCAGAGAAGA[A/G]CTGAATGAAATTGAG | 64326 |
rs143827990 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176135815 | ACCTCAGCTCAATCA[C/T]ACAGTCAGGTAAGTG | 64326 |
rs143829339 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | RFWD2 | GRCh38.p7 | 1:176016985 | TGTAAATATTACAGA[A/G]TAATTTCTAGTACAA | 64326 |
rs143830759 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176072860 | GTCAAAAATTAGTAT[A/T]AAAAATATTCATTAT | 64326 |
rs143859035 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176116334 | TACAGCATTCCAGCC[G/T]GCGTGACAGAGTGTC | 64326 |
rs143874474 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176179166 | ATATTGGTGCACACC[C/T]ATAGTCCTAGCTACT | 64326 |
rs143887626 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176176478 | CACGAGTCACAAAAA[A/G]CTGATTTAAAATTAT | 64326 |
rs143889005 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176056534 | TGTGTGTGTAAGACA[A/G]AGAGAGATTGATCTA | 64326 |
rs143896487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176109287 | TTCTATTGCTGTTTA[A/G]ATTATTGTTTAGCTG | 64326 |
rs143907322 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175972626 | CCCACGGCCATGCCC[A/G]GCTAATTTTTGTATT | 64326 |
rs143913510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176065650 | GCAGAACATAAACTC[C/T]TTTTGGGAAAGTGTT | 64326 |
rs143924323 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176006351 | TAGTCTATTTATATT[C/T]AAAGTTAATATTGTT | 64326 |
rs143953372 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176170119 | TCTAATTCTAGCTCT[C/G]TGGCTACTTCCTCCA | 64326 |
rs143954131 | snp | C/T | 6.61157e-05 | 0.00574922 | missense, intron-variant, utr-variant-5-prime | RFWD2 | GRCh38.p7 | 1:176175951 | ATATTGTCCACAACA[C/T]AGTTACACTTGGGAC | 64326 |
rs143960906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176101031 | AAGCTTCCCATTGCA[C/T]AGATAAAGGTCACGC | 64326 |
rs143979333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176077992 | CTGCTGAAAGAAATC[A/G]AAGATGACACAAATA | 64326 |
rs143995872 | snp | A/G | 0.000153988 | 0.00877328 | missense | RFWD2 | GRCh38.p7 | 1:176046280 | TTAATCTTCTTTGTA[A/G]CTCCAGCAATCGCAA | 64326 |
rs144006392 | snp | A/T | 0.0402882 | 0.136092 | intron-variant | RFWD2 | GRCh38.p7 | 1:176033149 | AGGTGCGGTGGCTCA[A/T]GCCTGTAATCCCAGC | 64326 |
rs144008183 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:176180469 | GTGGGCATAACAAAG[A/G]GGTAAAAGGGACACA | 64326 |
rs144009208 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176113398 | ATTGGATTATTATTT[G/T]TTGCAATCAAACTGT | 64326 |
rs144041809 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176178035 | GTATCATCACCTCTT[A/G]CAACTCTGACAAGGC | 64326 |
rs144070090 | in-del | -/TAAA | 0.195526 | 0.243993 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176145760 | CTGCACAAGCACACT[-/TAAA]TAACGCTCAAAAACA | 64326 |
rs144071235 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175978794 | AGAGTTGAAGGAAGA[A/C]AGAAAGAAAGAGAAG | 64326 |
rs144083282 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175978890 | TGGAAAGTTAGTATA[C/T]TTTTAGGAGTAGCAT | 64326 |
rs144099125 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176034798 | CTAAGCTCTAACTGG[A/C]ATGGGCATTAGGCAG | 64326 |
rs144099421 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176008551 | TTAATTACCTTTTTT[G/T]AATATATTTGTAATA | 64326 |
rs144104315 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:175973686 | CCCATTAGAGATGTG[A/T]TATACATAATTTCTA | 64326 |
rs144116974 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | RFWD2 | GRCh38.p7 | 1:176163947 | TTTTTGTTAAATGTA[A/T]CATGTAATTCTTCGG | 64326 |
rs144123177 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176065545 | CACCCCAAAATATGT[C/T]ACTCTGCCATAAAAA | 64326 |
rs144129765 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176130510 | GTTTGATTAATTCTA[A/C]GGAAAGTCTGAAATG | 64326 |
rs144131804 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | RFWD2 | GRCh38.p7 | 1:176031972 | CAGATTCAGTTCCAG[A/T]GTGCAAGGTTTATGT | 64326 |
rs144131988 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176066077 | CAAAAAAGAATCTAC[A/G]TAAGTCTTTCAAGAC | 64326 |
rs144135109 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175969509 | TCAACAAACAGGTCT[G/T]GCTAAGTTGCCCCCA | 64326 |
rs144150100 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176104116 | AACTTTTTAAAATAG[A/G]GCTGGGGGCACATAG | 64326 |
rs144162893 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | RFWD2 | GRCh38.p7 | 1:176125975 | ATTTAATTTTATTTG[C/T]GGCTTTATAAATAAG | 64326 |
rs144183427 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176197039 | AAAGAAAATCCCTAT[A/G]TTCTAACTCCCAGTA | 64326 |
rs144191837 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176063918 | AAGTAATGATAAAAC[A/G]TAAAATAGCCACTCA | 64326 |
rs144202653 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175966921 | CTCTCCTTCCAATCT[C/T]CCACCCCCCATACAC | 64326 |
rs144203660 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176012009 | CTCCTTCTATTAATT[-/A]AAAAAAAAACTGTAA | 64326 |
rs144214009 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | RFWD2 | GRCh38.p7 | 1:175998416 | TGTATACATATGTAA[C/T]TAACCTGCACATTGT | 64326 |
rs144214243 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:175963730 | AAGCCCAGCTCAAAA[G/T]CCCCTATCTTCATAA | 64326 |
rs144215309 | snp | C/T | 0.00398564 | 0.0444627 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207825 | CCAACGACTCCTGCT[C/T]TACTGATGGTGATTC | 64326 |
rs144220970 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | RFWD2 | GRCh38.p7 | 1:176019576 | TCAAAACATCACTAA[C/T]AGGGCCTGGCACGGT | 64326 |
rs144226183 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175961209 | TCATGTGAGCTAATA[A/C]CCCAAATAAAAACCC | 64326 |
rs144262610 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176012695 | TAACCTTATATTGTA[C/T]TCTTACTGTAGCTTT | 64326 |
rs144273111 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176056860 | TCTAGTGACTACAAA[C/T]ACTTTATTAATTACT | 64326 |
rs144288723 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176164754 | TTTCCCGTGAATCGA[C/T]ACATTTTCCATAATG | 64326 |
rs144291074 | in-del | -/C | 0.0134861 | 0.0810011 | intron-variant | RFWD2 | GRCh38.p7 | 1:176002152 | TTGCAAAAATACTGG[-/C]CATCATTTCTACAAA | 64326 |
rs144292147 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176109289 | CTATTGCTGTTTAAA[C/T]TATTGTTTAGCTGAA | 64326 |
rs144295451 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | RFWD2 | GRCh38.p7 | 1:176050275 | CATTAGTCAAGTGAT[G/T]AAGCAGCAAGGCAAG | 64326 |
rs144300630 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176098787 | CAAGTGTTTTAAACC[G/T]CTAACATATTTAACA | 64326 |
rs144330556 | in-del | -/CAAC | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176110666 | AACAAAAAAACAAAA[-/CAAC]AAAAAAAGATGACAA | 64326 |
rs144332110 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176159014 | GTAATTGTATTAAAA[A/G]CTCTAAAGCAACCAC | 64326 |
rs144333952 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RFWD2 | GRCh38.p7 | 1:175995109 | CTAAAAACCGCTCAA[C/T]TACATGGAAAGTGAA | 64326 |
rs144362242 | snp | C/T | 0.166832 | 0.235761 | intron-variant | RFWD2 | GRCh38.p7 | 1:175996163 | ACATGGTTACCTCAA[C/T]AGATGCAGAAAAGGC | 64326 |
rs144409238 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | RFWD2 | GRCh38.p7 | 1:176017445 | AGGTTTTTCTTAGGC[A/G]GGAAATAAATTTTGA | 64326 |
rs144418289 | snp | A/C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175959458 | CTGGCCATCAAAATA[A/C/T]GGCAAATGAATAAAG | 64326 |
rs144423034 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | RFWD2 | GRCh38.p7 | 1:176154186 | GCTTTTCTTTGTATA[C/T]CTGGCAGGGCTACTT | 64326 |
rs144449558 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176194191 | ATGGAAATCTTAAAA[A/G]TATCCAATTAATCCC | 64326 |
rs144451569 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | RFWD2 | GRCh38.p7 | 1:176154765 | TATATAACAAACCTG[C/T]ACATGTACTCCTGAA | 64326 |
rs144453612 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176086912 | GTACCCAAACAGAGA[G/T]ACAGACCAATCGAAC | 64326 |
rs144457295 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176086080 | AAACCAAATTCATTC[A/G]CAGAATGATTAAAAC | 64326 |
rs144461120 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176113047 | GCAGGTATCTCTTCC[A/T]TTCTTTTGGATATAT | 64326 |
rs144465409 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176000995 | TTGAAACATTATGGC[A/C]ATACATATTACATCT | 64326 |
rs144470747 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176037499 | CTGATATCAAAGTCA[C/T]GAAAAATTACAAAAA | 64326 |
rs144476689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176014213 | TCAAGTGGGAAGCTG[C/T]GCTTACATTTGAAAG | 64326 |
rs144476760 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176054021 | TCACTATCCTTAAGG[G/T]ATAGTGATCCTTAAG | 64326 |
rs144484210 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176190003 | AGTAAATAAGCATAA[A/T]GAATAATGATTTCAG | 64326 |
rs144495625 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176095369 | CTGGGAGGACAAAGC[A/T]ATGTTCTTAAAAATA | 64326 |
rs144501650 | snp | A/G | 0.0810805 | 0.184299 | intron-variant | RFWD2 | GRCh38.p7 | 1:176133154 | TACGTATATACGTAC[A/G]TATATATACGTATGT | 64326 |
rs144514866 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | RFWD2 | GRCh38.p7 | 1:176191049 | TTTGATACCAAATGC[C/G]AAACACTAGCAAATA | 64326 |
rs144548878 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175945406 | TTGGAAGCCTTCAAG[A/G]TAAACTACATAAAAC | 64326 |
rs144556672 | in-del | -/AGTTTATA | 0.0966517 | 0.197444 | intron-variant | RFWD2 | GRCh38.p7 | 1:176106443 | AAGATCAGAAATTAT[-/AGTTTATA]AGTTTATAAGTTAGG | 64326 |
rs144575224 | snp | C/T | 0.021333 | 0.101051 | intron-variant | RFWD2 | GRCh38.p7 | 1:176041121 | GATTTTAGTATACAA[C/T]AGAAATTAAATACAA | 64326 |
rs144579867 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175983102 | TTTAATCATTCCATA[A/G]TGTACATGTATATGA | 64326 |
rs144590688 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176194369 | TGTTGGCTGGGCGCA[G/T]TGGCTCACACCTCTA | 64326 |
rs144596072 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176009628 | TTGGAGTACTCATAA[C/G]CAGTTTGGTATGTTG | 64326 |
rs144600682 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175952337 | TGAGGTGGGAGAATC[G/T]CTTGAACCTGCGAGG | 64326 |
rs144610830 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176139003 | ATAATTGCTTTAAAA[A/C]ATACATTTAAAAAGA | 64326 |
rs144622399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176044382 | CAAGTACTCCAGAAG[C/T]CTACAACATCTAAAA | 64326 |
rs144623004 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176107474 | AGAAGTCAGTATGAA[C/G]GAGCTCCAACTAGCC | 64326 |
rs144623512 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RFWD2 | GRCh38.p7 | 1:176074517 | ATGTAGCATGCAAGA[C/T]GGCCCAACCAGAGGT | 64326 |
rs144633889 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176103412 | ACAATAAGATTGAAT[A/G]AGTTTCCAGGTTGGT | 64326 |
rs144635986 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:176043121 | TTGTATTTCTGCCGA[G/T]GAAAGGAATTACAGT | 64326 |
rs144654361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175947292 | ATTTCCTGGAGAGCA[A/G]TCCAAGAGATAATTT | 64326 |
rs144659165 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176176193 | CTGGGTAAACACTAC[A/G]CAAAAGTTATTTCAA | 64326 |
rs144677485 | snp | C/T | 0.0678174 | 0.1712 | utr-variant-5-prime, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207223 | CGAGGCCGCCGCCGC[C/T]ACCGCGGTCCCTGTA | 64326 |
rs144687557 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176042085 | CCACTGTACTCCAGT[A/C]TGGGCAGCAGAGCGA | 64326 |
rs144690923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176141691 | TGAAATGGCAGACCT[A/G]ATTAAAAGACTTCAT | 64326 |
rs144732500 | in-del | -/G | 0.093777 | 0.195178 | intron-variant | RFWD2 | GRCh38.p7 | 1:176018021 | CCTGCTCTCAATTTA[-/G]TTGTCAGATCTTTGT | 64326 |
rs144738382 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176077455 | AAAATCCAACATCCC[A/G]TCATGATAACAACCC | 64326 |
rs144741725 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176139579 | TCATTGCCCATCAAC[A/G]GTGGACTCAATAAAG | 64326 |
rs144768801 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176179510 | GAGGGCGAGGCAGGA[C/G]GATTGCCTGAGCCCA | 64326 |
rs144770892 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | RFWD2 | GRCh38.p7 | 1:176112881 | CCATCCATGTTGCTG[C/T]AAATGACAGGATTTC | 64326 |
rs144801445 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176075336 | TTAGCTAATGGCTTA[A/C]ATTTTAAGATCTTCA | 64326 |
rs144808845 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176029288 | TGGTTTTGTATTTGA[A/G]TAAGTAGTCTAAGCC | 64326 |
rs144810190 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176138252 | ACTGCTTAACATCAA[A/T]AAGTATAGTCAGAAG | 64326 |
rs144811828 | snp | C/T | 1.66369e-05 | 0.00288412 | missense | RFWD2 | GRCh38.p7 | 1:175989461 | GTGTTACGAAGATCA[C/T]AGTAGTGGACACAGT | 64326 |
rs144812780 | snp | A/T | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175969308 | CTCCAAATAGTCACC[A/T]TGGTATTTGAAAAAA | 64326 |
rs144816176 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176061743 | AAGCTAAAGTTATTA[C/T]AATGATAGAAGAAAA | 64326 |
rs144854530 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176135453 | TCAGGTGATAATCTA[C/T]TGATAAATGTTAAGA | 64326 |
rs144856527 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176176866 | AAAGAGTATATGTGG[A/C]TATGAACAATCTCAA | 64326 |
rs144871599 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176072447 | ACTGCTTTAAAAGAC[A/T]GATCCCAGGCAAAAT | 64326 |
rs144880436 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | RFWD2 | GRCh38.p7 | 1:175963446 | AGCAGAAAGGGTGTA[C/T]GTTTTACAGCCAGCC | 64326 |
rs144920932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176174755 | AAAGTAGTCACCACA[C/T]CCTAACTCTGAGCAT | 64326 |
rs144949272 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176051555 | ATACATTTATCATTA[C/T]TTTAGTGTATATCTT | 64326 |
rs144959536 | snp | A/C | 0.00716266 | 0.059414 | intron-variant, utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175967774 | ATCTTCACGGAAGCT[A/C]TCTCTGATTAGCTCC | 64326 |
rs144971347 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | RFWD2 | GRCh38.p7 | 1:175995320 | AATTGACACCCTAAC[A/G]TCACAATTAAAAGAA | 64326 |
rs144971693 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176111648 | TTCCAATCCTTAATG[A/T]TACTAAGTTTTACTA | 64326 |
rs145015231 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176059983 | GCTGACCTTAAACTG[C/T]TTTTTTAATAGCAAC | 64326 |
rs145023952 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176089699 | TTTTCTTTCTTGCCC[A/G]AATTCCTATTTAAGG | 64326 |
rs145027916 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | RFWD2 | GRCh38.p7 | 1:176032668 | GTGACAACGCAGATG[C/T]TTCTCCCAAACCAAG | 64326 |
rs145031057 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176087455 | AGAAGGGTATGAACA[C/G]ACACTTCTCAAAAGA | 64326 |
rs145034438 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | RFWD2 | GRCh38.p7 | 1:176028836 | ATGCCTCACTTCAGG[C/T]AGCCTCTACCTCCTA | 64326 |
rs145037843 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176030427 | CCCCACTTATAATCA[A/C]TAAAAACCTTTACAA | 64326 |
rs145049885 | in-del | -/A | 0.16846 | 0.236329 | intron-variant | RFWD2 | GRCh38.p7 | 1:176112175 | GCACTATCTCAAACC[-/A]AAAGTCTCCTTCACC | 64326 |
rs145054797 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176191665 | CTGAACCAATCTTCA[A/C]AGGCAGCAGTTAAGT | 64326 |
rs145064741 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176123495 | TGTGACTCTAAATGA[C/T]TCTAACCTGAAAGGA | 64326 |
rs145067530 | in-del | -/AAAT | 0.180064 | 0.240019 | intron-variant | RFWD2 | GRCh38.p7 | 1:175957154 | AAAGAAAACATTTTA[-/AAAT]AAATTAGTGTAGCTT | 64326 |
rs145075663 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176087815 | GCACATGTATGTTTA[C/T]TGCAGCACTATTCAC | 64326 |
rs145083745 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | RFWD2 | GRCh38.p7 | 1:176092196 | TATATGGCCAAATAT[A/C]AAATTTGATATAATG | 64326 |
rs145088823 | snp | A/G/T | 0.0240944 | 0.107291 | intron-variant | RFWD2 | GRCh38.p7 | 1:176086330 | TCCCAGTTTCTCGAC[A/G/T]TTCTCCTGCCTCAGC | 64326 |
rs145099206 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176026339 | TAATTGAATACATAA[A/T]ATTAATAATAAAAAT | 64326 |
rs145102215 | in-del | -/AT | 0.089084 | 0.191327 | intron-variant | RFWD2 | GRCh38.p7 | 1:176072782 | AACTATCATAGAAAC[-/AT]AAAGTTTAATTTGAA | 64326 |
rs145125202 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176119738 | ATACTACTACTTAAC[A/T]CCTGACTCATCCACA | 64326 |
rs145146287 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176190689 | TTTGTCATTCCCTTT[C/T]ATATGCATTATTTCC | 64326 |
rs145148561 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | RFWD2 | GRCh38.p7 | 1:175988745 | GGCTGAGGCAGGAGA[A/G]TCACTTGAACCTGGG | 64326 |
rs145152506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176120988 | TGGAATTATGAATAA[A/G]AGAATCAAAGAGAGT | 64326 |
rs145155395 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RFWD2 | GRCh38.p7 | 1:176155966 | CAGCCAGATGGATGC[A/G]AGAAAAAATGAAGAG | 64326 |
rs145170928 | in-del | -/TGTGAGTCATGGCATTAC | 0.40157 | 0.198813 | intron-variant | RFWD2 | GRCh38.p7 | 1:175977035 | TCACAAAGATATGTT[-/TGTGAGTCATGGCATTAC]TGGTGAGTCATGGCA | 64326 |
rs145208299 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176191624 | TCAAACTCTTCTTTA[C/T]ACCTATACCGATAAC | 64326 |
rs145211583 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RFWD2 | GRCh38.p7 | 1:176002000 | CCTGGTACTTGCTGA[A/G]CAACTTTTTGATTGC | 64326 |
rs145227461 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175956027 | AAAAAGCAAAGACAT[C/T]ATAATAGTTAAAATA | 64326 |
rs145227839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175985330 | ATTGTGCCCTAGTTA[C/T]TGTAGTTACAAAACT | 64326 |
rs145238539 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176098910 | GGGTAAACAGAACAC[A/G]TTTACTTACATGAGA | 64326 |
rs145243195 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175981625 | TTTTTGGCTAAAACT[A/G]CAAAAGCAAAAACAG | 64326 |
rs145267307 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176117644 | TCACGCCTGTAATCC[C/T]AGCACTTTGGGAGGC | 64326 |
rs145283634 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176200962 | CTCCTGGAGCTGAGA[A/C]TACAAGCATGCACCA | 64326 |
rs145289665 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176134871 | AAACAGATGGGCCAT[A/G]TGAATATCATTTCTA | 64326 |
rs145297158 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | RFWD2 | GRCh38.p7 | 1:176111483 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT | 64326 |
rs145301436 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176073749 | ACCTTGTGGACTGAA[A/G]GGTATGGTCTTAACT | 64326 |
rs145309843 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176010057 | CAGTCTGCAAAGAAG[C/T]TGAAAGAACAGCACA | 64326 |
rs145348851 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175983368 | GATGGTTTTAAAAAG[C/G]GGAGATTCCCTGTAC | 64326 |
rs145351193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176075057 | GCCCTAAAATAAGAT[C/T]GTGAGCTCTCCTGAA | 64326 |
rs145354415 | in-del | -/TCTC | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176099506 | TTTGGAGCATATTTG[-/TCTC]TCTCTCTCTCTCTCT | 64326 |
rs145356037 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | RFWD2 | GRCh38.p7 | 1:176012537 | AAAGAACTATTAACA[A/C]ATAAATTTAGTATAG | 64326 |
rs145356083 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:175979933 | AAAATTATATATTAA[C/T]TATGCATTATGTACA | 64326 |
rs145357215 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | RFWD2 | GRCh38.p7 | 1:176175663 | ACTGGTACCAGTCCA[C/T]GGCCCAGGGGTCCCT | 64326 |
rs145361393 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176108103 | GTAAAAAATTAAAAA[G/T]TAAAAATTTTAGGTT | 64326 |
rs145379854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175984702 | GAGGGAAGCTGTACC[C/T]TGCAACGCCACAGTG | 64326 |
rs145387428 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176065704 | AGGAAGGGGATAATG[-/A]TTTTTTTTTTTTTTT | 64326 |
rs145409927 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176075918 | TGAGGCAGGAAAATC[A/G]CTTGAACCTGGGAGG | 64326 |
rs145412168 | snp | A/C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176072225 | TTCTTCAAAGGAATA[A/C/T]TTTTCAACAAGCAAA | 64326 |
rs145415808 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176054107 | GAAGTTAAATAATTT[C/T]TCTTACTCTTCACAA | 64326 |
rs145418886 | snp | A/T | 0.084728 | 0.187577 | intron-variant | RFWD2 | GRCh38.p7 | 1:175993300 | AGATGGGGAAAAAAC[A/T]AAGCAGAAAAACTGG | 64326 |
rs145420623 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176009258 | CAATACTGTGGGTAT[C/T]GACAGGTATTTTCCC | 64326 |
rs145423534 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | RFWD2 | GRCh38.p7 | 1:176173217 | TAGGGAGGCTGAGGC[A/G]GGAGAATCATGTGAG | 64326 |
rs145434602 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176141158 | ATAATTGTTCCAAAC[A/T]GAACAAAAGAATACA | 64326 |
rs145439396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176177688 | ACCTCTTTTATTACG[C/T]ATCCAAATTACTATA | 64326 |
rs145462837 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176174266 | CAGAAAAAGCATAGT[C/G]ATCTTTAGTGATCCT | 64326 |
rs145513516 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176079167 | AAAGTAAGTTGTTCT[A/T]CCATAAAGACACATG | 64326 |
rs145534287 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176105602 | AAAGGACAAATGCCA[G/T]AATGAACCCTAAACA | 64326 |
rs145539204 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176181390 | CACATGTTAGGAAAG[A/T]GTAAATAATTATAAA | 64326 |
rs145543740 | snp | C/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207393 | CCTGGCGAAGGGAGT[C/G]TGTCTGTCCCAAGCC | 64326 |
rs145548498 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176114032 | TCTTGCTTTTTGTTT[C/T]GCTTCATCAGTCACA | 64326 |
rs145549407 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176088545 | ATACATAAGATCTGC[A/G]CTTTTCTTTATATGT | 64326 |
rs145580526 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176031811 | GTTCGATTTTGAAAT[A/C]CTGAATCTTAAAAAA | 64326 |
rs145583834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176171801 | AGTCAGAATTTCAAG[C/T]ACGGAAATAGATTAT | 64326 |
rs145589074 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant, utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175971147 | TGGGGTTTTAGACTT[A/C]AATGACTTAGAAAGA | 64326 |
rs145596190 | in-del | -/TTAG | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176083702 | AATAGTTGGAAATAA[-/TTAG]AAGAGAATACAGATG | 64326 |
rs145601728 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | RFWD2 | GRCh38.p7 | 1:176102556 | TCATTCCTGGGCATA[A/G]ACTGAACTGACTTTG | 64326 |
rs145608769 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:176125629 | TTGGTTACTATAGCT[A/G]TATAGTATAATGTAA | 64326 |
rs145627602 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | RFWD2 | GRCh38.p7 | 1:176028422 | ATACAAAAGTTAGCT[A/G]GGCATGGTGGTGCAG | 64326 |
rs145632669 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175968926 | TGGATGATCTTCTGA[A/G]TAAAGCTTGAGAAAA | 64326 |
rs145660641 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176061153 | AGTTAAGTAGACTCA[C/T]ATATATACAGTCAAT | 64326 |
rs145661162 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176205534 | CTGTGCAAGCAGCCA[A/G]CTTCCTACATGCCTA | 64326 |
rs145719085 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | RFWD2 | GRCh38.p7 | 1:176160411 | CAACAAAAGCCAAAA[C/T]TGGCATATGGGATCT | 64326 |
rs145722934 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176035668 | AACAGAGAAATAAAA[C/T]CAGACTTTAACATTT | 64326 |
rs145728926 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:175974611 | TAAAACGTTTAAGAT[C/G]GAATAGGTAATTTCA | 64326 |
rs145738598 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:175987784 | TGTATCAGAGCATTT[A/G]AATAATATCAAATTT | 64326 |
rs145740811 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176199310 | CGACAGTATGAGACT[C/G]CCATCTCAAAAAAAG | 64326 |
rs145753899 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176131290 | ATTATTGCTAGATGA[A/G]GTGATGCTAAGGATC | 64326 |
rs145757932 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176066607 | GGCTGCTGACTTTTA[A/C]GTCAAGGTGAGATGG | 64326 |
rs145764298 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176157340 | GCTACAATGAAATCA[C/T]AATCAATTTCAAAGG | 64326 |
rs145766286 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176195784 | CGGATTAACACAAAA[A/C]CAGAAAACCAAATAC | 64326 |
rs145786624 | snp | A/G | 0.00159617 | 0.0282053 | | | GRCh38.p7 | 1:176171507 | GCCTTCTTATCATTC[A/G]TGTCTTCACTGGAGT | 64326 |
rs145860725 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176072480 | GGGAAGGAAATCCCT[C/T]CCTCTGCACTCCCAT | 64326 |
rs145867849 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176106885 | ACTAGCTCACAATTA[A/G]AGACTCCAACCAAAA | 64326 |
rs145875727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176021648 | CTCAAAAATCTGGGA[A/G]ATGGTTGTCTACATT | 64326 |
rs145881477 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176192471 | CCCGCTTACAATATA[C/T]AGCCCCTTCAGCACC | 64326 |
rs145886969 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176174801 | GCAGAATTGACCTTT[C/T]TGATATATAATCCCA | 64326 |
rs145895330 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175960139 | AACTGGTTTTCAGGA[A/G]GAAATGGACCAGAAT | 64326 |
rs145901151 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176181736 | ATCCCAGCTACTCGG[A/G]AGGCTGAGGCAGGAG | 64326 |
rs145911414 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175957277 | AGCAGCTTCTACTCC[A/G]CCAAGCTCCATTCAT | 64326 |
rs145923607 | snp | C/T | 0.021333 | 0.101051 | intron-variant | RFWD2 | GRCh38.p7 | 1:176054709 | TTTCCCTCCTCTCTC[C/T]TGTATCAATCAATTT | 64326 |
rs145926022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176185332 | TTAAAGTCACACAGC[C/T]AAGAAGTAACAAAGT | 64326 |
rs145941107 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:175949753 | GGACAATGAAAAATT[A/T]AAAGCCGAAAGCTCC | 64326 |
rs145975506 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176040650 | AGGTATTCCATTCTG[C/T]ATATAGTAGGAATAA | 64326 |
rs146010710 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176038032 | ACGTAATTGGCTATG[C/T]AGAAAATCCCAAGGA | 64326 |
rs146031945 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176130518 | AATTCTACGGAAAGT[C/T]TGAAATGGATGAAAG | 64326 |
rs146037418 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176052375 | AATGCAGGACTGTAT[C/T]TGAGAAATTCACAGA | 64326 |
rs146049924 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176170603 | CACGCTGAAAAGAGA[C/T]ATGCTGTCTTCAGGC | 64326 |
rs146067246 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176083457 | AAGTATAGTAATTGA[C/T]TTTAACTTATGAGGT | 64326 |
rs146098356 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176024459 | ATAACAAAAACTCTT[A/T]GCAAACTAGGAACAG | 64326 |
rs146098711 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:175991007 | TTGCACATCTGAAAT[A/C]AAAAAATCCCAAATC | 64326 |
rs146134250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176020708 | AAATTATATTGTGGG[C/T]TTTATCACTGGGAAA | 64326 |
rs146149995 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | RFWD2 | GRCh38.p7 | 1:176115937 | GGTCTTTATTCCATG[A/G]AAAAGCTGTTAAGTT | 64326 |
rs146153480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176113149 | TTCATAATGGCTGTA[C/T]GACTTTACATTCTCA | 64326 |
rs146153739 | snp | A/G | 0.021333 | 0.101051 | intron-variant | RFWD2 | GRCh38.p7 | 1:176152112 | CCTGGGCAACATGGC[A/G]ACACCCCATCTCTAC | 64326 |
rs146174482 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176147540 | AGTATTTGGAACTAG[C/T]ATGTTTCTTGGTTAA | 64326 |
rs146184432 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176186935 | TGACTACAGGTTTAC[C/T]TCGCACACAGCTCCA | 64326 |
rs146197634 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176079780 | CAAAATCTTAACCAC[C/T]GCTGAATGTGGGTGA | 64326 |
rs146202059 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175978639 | CCATGCTCAGAATCT[G/T]CTTTCATTCTACTCC | 64326 |
rs146218527 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | RFWD2 | GRCh38.p7 | 1:176069151 | GATTGCACGACTGCA[C/T]TCCAGCCTGAGCAAC | 64326 |
rs146235890 | snp | A/G | 0.0531913 | 0.155826 | intron-variant | RFWD2 | GRCh38.p7 | 1:176008043 | GCGGGATATAATCTC[A/G]TGGTGCGCCGTTTTT | 64326 |
rs146251131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176103870 | GAGATAATTGGTAAG[A/G]TAAAGGCAGTTCCAA | 64326 |
rs146251479 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | RFWD2 | GRCh38.p7 | 1:176065991 | TCGGCCTCCCAAAGT[G/T]CTGGGATTACAGGCA | 64326 |
rs146266303 | in-del | -/AAAT | 0.179168 | 0.239756 | intron-variant | RFWD2 | GRCh38.p7 | 1:176165687 | CTAGACTCCATCTCA[-/AAAT]AAATAAATAAATAAA | 64326 |
rs146267396 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176170267 | CATGAGTGTTCTTAA[C/T]GGCATCTAGAATGGT | 64326 |
rs146269841 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176101212 | GGCACCCTATCGTGG[C/T]TGGTGGGACTCGGGA | 64326 |
rs146282869 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175956495 | CATGTACAATAAAGG[-/A]AAAAAAAAACCCTGA | 64326 |
rs146286437 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176166627 | TGAAAAAATGGTTAT[C/T]TTTTTCTTCTTGAAA | 64326 |
rs146286598 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | RFWD2 | GRCh38.p7 | 1:176202707 | AACCAGTTATATTAA[C/T]AAGAATGGTCAACAG | 64326 |
rs146290543 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | RFWD2 | GRCh38.p7 | 1:176200382 | TTTACAAAGCCTACT[A/T]TGTCTCATTATCTCT | 64326 |
rs146302307 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175965466 | GTTGATTTCCTGACA[C/T]GCAGAATCATTCTTT | 64326 |
rs146313356 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176182765 | TACCTGTATCAGCCC[C/T]GAAGCAAGACCCACA | 64326 |
rs146313962 | in-del | -/G | 0.0930568 | 0.194599 | intron-variant | RFWD2 | GRCh38.p7 | 1:176083441 | TTTTTCAGTATCTGA[-/G]AAGTATAGTAATTGA | 64326 |
rs146322218 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | RFWD2 | GRCh38.p7 | 1:175961789 | TACTTGGAAAAGATA[A/T]GAAAGGCTTCACAGA | 64326 |
rs146358358 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175994472 | ATAAAGAGTCAAGAC[C/G]CATCAGTGTGCTGTA | 64326 |
rs146375045 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176087697 | TGGAAGACAATGTGG[C/T]GATTCCTCAAGAATC | 64326 |
rs146376941 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992971 | CCCCTGACCCCCAAG[C/T]AGCCTAACTAGGAGG | 64326 |
rs146389109 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176154031 | CATGGATGTGAATCA[A/G]TAACACTGGTCTTAA | 64326 |
rs146393422 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176085370 | TTTATCTGTTGCTTT[C/T]CCTGACTCGATTTAC | 64326 |
rs146406588 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176189305 | CAGTCCATTTTGAAA[C/T]ATTAGATTATAATTG | 64326 |
rs146413203 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176144958 | GACCACAGGTGGAAA[A/G]GACTTCTTTAAGTGA | 64326 |
rs146413748 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | RFWD2 | GRCh38.p7 | 1:176078112 | ATCCTTAAAATACCA[A/G]CGTCATTTTTCACAG | 64326 |
rs146437773 | snp | C/T | 4.96282e-05 | 0.00498113 | missense, utr-variant-5-prime, intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176175993 | TCCTCCAAACTCTGA[C/T]GAATACACTTGTAGC | 64326 |
rs146447727 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | RFWD2 | GRCh38.p7 | 1:176141484 | CCAGCCTGGGCAACA[C/G]AGCAAGACTCCATCT | 64326 |
rs146448197 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176180707 | TCTATGTAAACAAGG[A/T]TGAGTAGATATAAAC | 64326 |
rs146467302 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176178106 | GAAAATTTCCTACAT[A/G]GAAATTTCACTGAAG | 64326 |
rs146481142 | in-del | -/AT | 0.0955749 | 0.196603 | intron-variant | RFWD2 | GRCh38.p7 | 1:176193440 | CCAGAGACTAGAAAC[-/AT]GTGTTAAAACAAAAA | 64326 |
rs146503271 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175973769 | AACACTCTAATATTT[C/T]TGTGGCTACAAAACT | 64326 |
rs146516864 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176034982 | CATTTCCCACACAAT[G/T]TAAACAGGACCCAAC | 64326 |
rs146519911 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176032070 | TTACCAAAGAAAGAG[A/T]AAACAGGGACAGAAG | 64326 |
rs146520274 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176066125 | CCATCAGTTTCCCCA[C/T]ATATGTGTTGACCCT | 64326 |
rs146522126 | snp | C/T | 0.495095 | 0.0492773 | intron-variant | RFWD2 | GRCh38.p7 | 1:176005154 | tagaggtgtttgtag[C/T]attctctgatggtag | 64326 |
rs146523255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175971208 | AATATGTCAAAGTTG[A/G]AAGGGTATTTTGTAG | 64326 |
rs146537710 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176126041 | TGGCATATAAACATG[C/T]TACTGATTTTTTGTA | 64326 |
rs146570820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176167287 | AAAAGCAATGCTTAC[C/T]TATTAGCAGAAGACA | 64326 |
rs146571184 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176123154 | GATACAATCCATCAG[C/G]GTTTAAAAAAACAAT | 64326 |
rs146588966 | snp | A/G | 0.030665 | 0.119967 | intron-variant | RFWD2 | GRCh38.p7 | 1:176164857 | TTTTTTTTAAAAAGG[A/G]AAACTACCACTAGGC | 64326 |
rs146618166 | snp | A/G | 0.000329698 | 0.0128351 | intron-variant | RFWD2 | GRCh38.p7 | 1:175988461 | AAAATTTCTTGGCAC[A/G]AAACTCATCACTACT | 64326 |
rs146639873 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176014222 | AAGCTGCGCTTACAT[A/T]TGAAAGGCTGCTTTA | 64326 |
rs146642182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175957337 | TTACCTTTTATATTG[C/T]ATTTTTACTATAGCT | 64326 |
rs146673371 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176051219 | ATGAACCGTGAATAT[C/T]TTCAGCCATCAAATG | 64326 |
rs146706882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176145934 | TCTAGCAGTATTGCA[C/T]TGTGCTTACAATGGT | 64326 |
rs146735323 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176067227 | AAACTGATATGGGAG[-/A]GGGGCAGTGAAGTGC | 64326 |
rs146741614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176001943 | GTAATGATTTCTGAC[A/G]AGAAGTCATCAGAAA | 64326 |
rs146741733 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175968609 | AATTAACTAACTGCA[G/T]CAAATTCTCATTTAA | 64326 |
rs146742865 | in-del | -/TGTG | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176127561 | GGAATAGTATTCTAC[-/TGTG]TGTGTGTGTGTGTGT | 64326 |
rs146743776 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175980398 | TTCAATGTTTCAGAA[C/T]AGTATTTCATCATAT | 64326 |
rs146757004 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | RFWD2 | GRCh38.p7 | 1:176097237 | TTGTTGAAAAAAAAA[C/T]GACTGAATTATTTTT | 64326 |
rs146759289 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176061090 | GTAATCATGACAGTA[C/T]GGTACTGGCCTAAGA | 64326 |
rs146771902 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175977241 | ATGTGTAAAGACTTT[A/T]TCATTTAAACCAAAG | 64326 |
rs146774429 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176164342 | TAACTATCCAAAAAC[C/G]ATCCTACTCTTTTTC | 64326 |
rs146779053 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176092586 | GACAAAACATAAAGG[A/C]CAATAAATATAAGAA | 64326 |
rs146811678 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176089937 | GTATTAACATAACTA[C/T]ACCCTTCCCCTTCCA | 64326 |
rs146826140 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176195492 | TTGACATGTATAGAA[A/C]CTCAGCCTACACATG | 64326 |
rs146840689 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175959285 | AGAACTCTCAGCACA[C/T]TGAGAACTGAAGGAA | 64326 |
rs146842196 | in-del | -/ACACAAAGAAA | 0.0448719 | 0.142907 | intron-variant | RFWD2 | GRCh38.p7 | 1:176204120 | AAACTCTCTAATTGC[-/ACACAAAGAAA]ACACAAAGTTGAGAA | 64326 |
rs146860134 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175956641 | ATTTTAGGATGCTGG[C/G]AGGAGTGCAAAATAT | 64326 |
rs146863206 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176036858 | TCAATTTATGATGGA[C/T]TTATTGGGACTGTAA | 64326 |
rs146864329 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175991507 | GACGTTAACAGTATA[A/C]CTAGGCTACACTAAA | 64326 |
rs146864694 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175952131 | GCATCTTTAAGATGA[C/T]AAACAAGAGGCCAGG | 64326 |
rs146876912 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | RFWD2 | GRCh38.p7 | 1:176050650 | AAAAATACAAACACA[A/T]GTAAAGTAAATTAAG | 64326 |
rs146880802 | snp | C/G/T | 0.000100586 | 0.00709111 | intron-variant | RFWD2 | GRCh38.p7 | 1:176046144 | ATGCAAATTGTTACA[C/G/T]CTATACTGCATCATG | 64326 |
rs146881912 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176081976 | GGTACAGTATACAAA[A/T]ACCTTGGGTAAAGTC | 64326 |
rs146890389 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176067574 | CGGCCCGACTCCAGG[G/T]GAAACCCACTTTCCC | 64326 |
rs146901087 | in-del | -/AAAAT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176155632 | TCGCTGCCAAAAAAC[-/AAAAT]AAAATAAAGAACAGA | 64326 |
rs146906610 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176128823 | TTGAACCAATAATAA[A/C]TGCCAAAAAGTACTA | 64326 |
rs146909790 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176065552 | AAATATGTCACTCTG[C/T]CATAAAAATTCTTTT | 64326 |
rs146923134 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:176169551 | TAAAAGTTCTGTTTA[C/T]GCTATACCGTAGTTT | 64326 |
rs146979007 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176022088 | ATTACATACACAAAG[C/T]TCAGAAGACATATGT | 64326 |
rs146985122 | snp | A/G/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175960760 | TTTGACAGAGGCTTC[A/G/T]CCAGAAAGCTACTCC | 64326 |
rs146996533 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176018981 | GACGAGCCTGGCCAA[C/T]GTGGTGAAACTCTGT | 64326 |
rs147014424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176112355 | TTTAGGGTACATGTG[C/T]ACAACGTGCAGGTTT | 64326 |
rs147016260 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176052782 | ACGCATACACGTATT[C/T]GGTTTTTTTCAATTA | 64326 |
rs147043622 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176152709 | GCCTCCCAAAGTGCC[A/G]TAATTACGGCGTGAG | 64326 |
rs147055563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175975175 | AAAATACATAGGATA[C/T]ATAAAAGCTTCTAAG | 64326 |
rs147066114 | in-del | -/GAG | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176005752 | CTTTTACATTTGCTG[-/GAG]AGAGCTTTACTTCCA | 64326 |
rs147081931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176066895 | TCCGCCCTTGGAACA[A/G]TTGGTTACCAGCTGT | 64326 |
rs147084768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175971724 | AGAACACAGTACCTT[C/T]CAGGAGGCAGATCTT | 64326 |
rs147093767 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175955764 | AATCATTTAGAGACA[A/C]ACCACACACACACAC | 64326 |
rs147101081 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176002344 | ATTCTTTCTTTTTTA[A/G]TTTTTATTTATTTAT | 64326 |
rs147102750 | snp | A/C | 0.0189856 | 0.0955633 | intron-variant | RFWD2 | GRCh38.p7 | 1:176099752 | AGCCCCTTGGGAAAA[A/C]TGGCCTCATACCCTT | 64326 |
rs147113985 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | RFWD2 | GRCh38.p7 | 1:176168259 | TGACAGGATTTCACC[A/G]TGTTGGCCAGGCTGG | 64326 |
rs147117311 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176201901 | AAGTTCTTGACAGAT[A/G]TTACTATAATAATAT | 64326 |
rs147117538 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176094341 | GCAACACTTGGGTCA[A/T]CATCATATGCCAGTT | 64326 |
rs147153955 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:176030778 | CAAAACAGGTGTTAA[C/T]TGTGTTCCCCAAAAA | 64326 |
rs147162629 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176196441 | CACCATTAACAAATC[A/C]AAGACATTAAAAGAA | 64326 |
rs147163211 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176129337 | AAATCAAAAGTGTCA[C/T]ATAAAAGTCTTACCT | 64326 |
rs147163608 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | RFWD2 | GRCh38.p7 | 1:176088087 | GGAAGGGGAACATCA[C/T]ACACCAGGGTCTGTC | 64326 |
rs147167111 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176125333 | AAAATTTTTTGCCCC[A/G]AGTTTCCCCAATGTT | 64326 |
rs147178772 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176193972 | TTTAAACAAAAGGAA[C/T]AGAGAACTAACACTT | 64326 |
rs147193166 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175953733 | CCAGCGATAAAGACA[G/T]GTATTTCATAATTAA | 64326 |
rs147209765 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | RFWD2 | GRCh38.p7 | 1:175950617 | TTACTTGCTAAATAA[A/G]ATAAAAGTGTGAGTC | 64326 |
rs147209850 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175990103 | TACACAATTCTCTAT[A/C]AACACTGCTTTGGCT | 64326 |
rs147224399 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176044082 | GCCTAGAGCTATCAC[C/T]GGCCATCTTTGATAC | 64326 |
rs147254557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176077000 | AAAACAAAAAACTAC[C/T]AACCAAAAAGAGCCC | 64326 |
rs147271542 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176075063 | AAATAAGATTGTGAG[C/G]TCTCCTGAATCCAAG | 64326 |
rs147284784 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176176512 | CTAGATTTTACCAAT[C/T]AGGATGGAAAAATAA | 64326 |
rs147292355 | in-del | -/AAC | 0.166832 | 0.235761 | intron-variant | RFWD2 | GRCh38.p7 | 1:176189803 | AATATGACCAAAACA[-/AAC]AACAATCATAATCTA | 64326 |
rs147331039 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176030054 | ACTCCTGAATTCAAG[C/T]GATCCTCCCATGTCA | 64326 |
rs147344824 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176125139 | TTTTCTAAGCTCCTC[A/G]TATATTCTGGTTATT | 64326 |
rs147347180 | snp | A/G | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175969599 | TCATTTCTTCATCAA[A/G]CCTAAGCATAAACAT | 64326 |
rs147360851 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176062154 | TACAGGCGCCCGCCA[C/G]CACGCCTGGATAATT | 64326 |
rs147376515 | snp | A/C | 0.0189856 | 0.0955633 | intron-variant | RFWD2 | GRCh38.p7 | 1:176120598 | TGCTAAAAAAAGTAA[A/C]AACAATGCAGCTGTT | 64326 |
rs147421078 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176016066 | GGGTTTGCAAAAGAA[A/T]AATTGAGTTCTGGAT | 64326 |
rs147422991 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | RFWD2 | GRCh38.p7 | 1:175958482 | TCATTCCTCTCTCCC[C/T]GTTCAATATAGATGG | 64326 |
rs147437023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176011556 | AGTATGCTTATCATA[C/T]CATCTTAACAATCAA | 64326 |
rs147452522 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:175954343 | TGAACATTAATGATA[C/T]AGTAACTTGCACCTT | 64326 |
rs147466934 | snp | A/C/T | 0.0410537 | 0.137264 | intron-variant | RFWD2 | GRCh38.p7 | 1:176049165 | GCCTGGGCAACAGAG[A/C/T]GAGACTCCGTCTCAA | 64326 |
rs147481704 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176148162 | ATCACAACTAAATTA[A/G]CAACAGTTGAGAATA | 64326 |
rs147481794 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176105463 | AAATATCTCTAGTTA[C/G]ATTGGTTTTCTCAGC | 64326 |
rs147482700 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176044623 | AATTATCTGGAACAA[C/T]TAAGAGACACATTTT | 64326 |
rs147484791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176144239 | AAATTAGGATTAATG[A/G]GAGTTTAACCAGGTT | 64326 |
rs147496368 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176208409 | GAGGCTGTAGGGAGC[A/G]GAGATCCCTACACTC | 64326 |
rs147497327 | in-del | -/AGA | 0.093417 | 0.194889 | intron-variant | RFWD2 | GRCh38.p7 | 1:176027968 | ACTCACAACAATGGC[-/AGA]AGGTGAATGAGGAGC | 64326 |
rs147499353 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176204796 | CAGGTGTGGTGGCAG[A/G]TGCCTGTAATCCCAG | 64326 |
rs147526246 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | RFWD2 | GRCh38.p7 | 1:176000487 | ATGTGAGTAATGTCT[G/T]CACTATGAAGTTATA | 64326 |
rs147572336 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175994988 | AAAATTGACCACATA[C/G]TTGGAAGTAAAGCTC | 64326 |
rs147592036 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176026435 | TCTACCTCTATGTTA[A/C]AGATAAAAAACTTGG | 64326 |
rs147605484 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176121540 | ATGTTTTTAGAGGTA[C/T]GATCTCACTCTGTCA | 64326 |
rs147620437 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176186741 | GTGTAGAAATGGTTA[C/T]GGAAGCTATCATAAT | 64326 |
rs147621809 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:176022756 | CGAGGAAAATTAGCT[C/T]ATACCTAACCTCAAT | 64326 |
rs147678243 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:175983581 | AGAAGTGGGGTGCTG[A/C]TGAAAAGATACCCCA | 64326 |
rs147681332 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | RFWD2 | GRCh38.p7 | 1:175980086 | TAACAACCCTAGAAG[A/G]TAAGTGGCTATTATT | 64326 |
rs147695603 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176072228 | TTCAAAGGAATATTT[A/T]TCAACAAGCAAATAT | 64326 |
rs147697901 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:176009375 | TTTCATAAGATGAGA[A/G]TAATTTGGTATTATA | 64326 |
rs147708173 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176174471 | CATAAAACTTTAGCC[A/G]CTTAGAAGAATTTGT | 64326 |
rs147712551 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176105621 | GAACCCTAAACATGG[C/T]AGAATAGCATGGATT | 64326 |
rs147726841 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | RFWD2 | GRCh38.p7 | 1:176005329 | CCTTAATTTTTGTAG[A/G]GTTTTTTGTGTCTCT | 64326 |
rs147741703 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176102761 | CTTAAACTGTTCCTA[A/G]GATCAGTGCTTGAGA | 64326 |
rs147753452 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176205929 | GGTGGAGAAGTGAAA[A/C]ATCTGTTAACAGACT | 64326 |
rs147759856 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176202008 | AGCTCACAATGGTCT[A/C]AAAAGAAAAGTCACT | 64326 |
rs147780132 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176025910 | CAAAAAAAAAGAAAA[C/T]CCAAACAAATAAAAA | 64326 |
rs147782668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RFWD2 | GRCh38.p7 | 1:175967053 | TCCTTCCTTACAAAA[C/T]CTTAAAATCGTTCAT | 64326 |
rs147786305 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175963853 | GGGTTCATACTATAG[C/T]TATTTATGAATATTT | 64326 |
rs147797564 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176021884 | ATGTCTGATTGAAAA[C/G]AACGTGGATTTCTCT | 64326 |
rs147798779 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176117300 | TTTGTAACCCAAAAC[C/T]AATATACTAGTTTCC | 64326 |
rs147801131 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176056979 | TACTCATCATATTCA[C/T]TGTCTCACAATCTAC | 64326 |
rs147815868 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176159522 | ACAAGGAGAAAGGTA[C/T]ACTAAATGTAGTGCT | 64326 |
rs147817274 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176054829 | ATATCTATTTTAGCT[A/G]CTATCCTATTGCTTT | 64326 |
rs147845296 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | RFWD2 | GRCh38.p7 | 1:176155160 | ATTAAAATGTAAAAG[G/T]TTACTTCCACAGTAA | 64326 |
rs147861210 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176191054 | TACCAAATGCCAAAC[A/T]CTAGCAAATAACCAC | 64326 |
rs147884614 | in-del | -/C | 0.00597247 | 0.0543191 | intron-variant | RFWD2 | GRCh38.p7 | 1:175977001 | TTAGTATTTTTTTCT[-/C]CCAATCTCTGGAAAT | 64326 |
rs147886724 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176008793 | AATCTGTTCAGCCTG[A/T]AATTCCTACTGCATG | 64326 |
rs147888828 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175950848 | CTACACTAACTTATA[C/T]CAAAACATTTTTAGT | 64326 |
rs147898019 | in-del | -/GCA | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:175974881 | CAATGAGCCATGGCT[-/GCA]CTGCACTACAGCCTA | 64326 |
rs147901226 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | RFWD2 | GRCh38.p7 | 1:175947394 | TTTTTTTTTTGAGAC[A/G]GAGTCTTGCTCTGTT | 64326 |
rs147903183 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | RFWD2 | GRCh38.p7 | 1:176004888 | AGTTAGGGAGGATTC[C/T]CTCTTTTTCTATTGA | 64326 |
rs147903557 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176102463 | TCTGAAACTGCCACT[A/G]CAAAATTACAGCTAA | 64326 |
rs147906246 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | RFWD2 | GRCh38.p7 | 1:176042163 | ATAATCCCAGCTAAA[C/T]GGGAGGTGGAGGCAG | 64326 |
rs147914656 | in-del | -/G | 0.172351 | 0.237636 | intron-variant | RFWD2 | GRCh38.p7 | 1:176065755 | TCCGTTGCCTAGGTT[-/G]GGAGTGCAGTGGCGC | 64326 |
rs147920190 | snp | A/C | 0.0189856 | 0.0955633 | intron-variant | RFWD2 | GRCh38.p7 | 1:176099462 | TACAGTCTTTAATAA[A/C]TGAGTATGGCACACT | 64326 |
rs147920486 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176139791 | GGTTACAACAGACAC[A/T]GGGAACTACTGGGGT | 64326 |
rs147936506 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176201192 | CTAAAATTCGAAAAC[A/C]AAAACCAAAAAAACC | 64326 |
rs147937355 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176039342 | TCATAGCACTGAATA[A/C]ATATATTAGAAGATC | 64326 |
rs147950484 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176135672 | ATCAACCATTATATA[A/C]ATTTTCTCTCTCACA | 64326 |
rs147970523 | in-del | -/TTTCAA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176171676 | AGGGTTGCCACAAAC[-/TTTCAA]TTTGTTAAAAAAAAT | 64326 |
rs147972306 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176103349 | CAACCTCCAGGAAGC[A/G]GGTGAGGCCTGGAGA | 64326 |
rs147980718 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | RFWD2 | GRCh38.p7 | 1:176196239 | AACTCCAAGTTAGCA[A/G]AAGAAATTTATAAAG | 64326 |
rs147985707 | in-del | -/GT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176056512 | TCATTATAATGGGGC[-/GT]GTGTGTGTGTGTGTA | 64326 |
rs148009665 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176010091 | AATAACCTTGTACCA[C/T]TTGTTCTAGACTCAC | 64326 |
rs148011659 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175952841 | AGGATCTCTTGAGCC[C/T]AGGAGTTTGAGGCTG | 64326 |
rs148017269 | in-del | -/TG | 0.410737 | 0.191478 | intron-variant | RFWD2 | GRCh38.p7 | 1:176127602 | GTGTATGTGTATATA[-/TG]TGTGTGTGTGTATAT | 64326 |
rs148022515 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | RFWD2 | GRCh38.p7 | 1:176133180 | TATGTACACACATAC[A/G]TATATACGTACGTAT | 64326 |
rs148022687 | in-del | -/TC | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176192154 | TATGGCCAAGAAGTA[-/TC]TCTGCTGATTCCTCT | 64326 |
rs148022949 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176108424 | TATACAATCTTTACA[C/T]AGTACTTAGAATCAT | 64326 |
rs148026428 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176048707 | AAATACTTTTTCTCC[A/G]CCTACTCATATACAT | 64326 |
rs148030901 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176199894 | TCAACTACACACTTA[C/T]GACCAGTGACTTATT | 64326 |
rs148039245 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176147492 | TATTAATGACAGTAC[A/G]ATCACTGTACACTAG | 64326 |
rs148043617 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RFWD2 | GRCh38.p7 | 1:175964736 | TACAGTATCTGCAAA[C/T]ACAGCTCCCTGGAGG | 64326 |
rs148078541 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176052783 | CGCATACACGTATTT[A/G]GTTTTTTTCAATTAA | 64326 |
rs148088672 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176176466 | AACCATCATCTTCAC[A/G]AGTCACAAAAAGCTG | 64326 |
rs148092786 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176153595 | CTTTCTATGCTTGAC[C/T]GCTCCAGCCAAGACT | 64326 |
rs148112704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175999560 | TACTGCGAACAGTGC[C/T]GCAAAAAACATGGGA | 64326 |
rs148115425 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176036097 | ATGAAAATAATATAA[C/T]AGCAAATATAATAGT | 64326 |
rs148123410 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176188056 | CAGGCACTGCCTGTG[G/T]ATCAGGAATCTAGCC | 64326 |
rs148161158 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | RFWD2 | GRCh38.p7 | 1:176087698 | GGAAGACAATGTGGC[A/G]ATTCCTCAAGAATCT | 64326 |
rs148162255 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176029305 | AAGTAGTCTAAGCCA[C/G]TGATATATATTAAAA | 64326 |
rs148170563 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175980870 | TATCTGCAGCCTCAA[A/T]AGAAGTTACTATGGA | 64326 |
rs148174208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176192656 | CACAGGCCAATCAAC[C/T]GGGGAAGATACCAAG | 64326 |
rs148178282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176124969 | GTCATTTTAACTGAG[A/G]TGAGATGATATTTCA | 64326 |
rs148184760 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176073215 | AATATTTATGATGTT[A/G]TCTAAAAATGAGTAG | 64326 |
rs148222923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175985914 | TGGATTTTTAAATTA[C/T]ATATCAAGTCAGAAT | 64326 |
rs148223719 | in-del | -/GA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176172440 | TCAAAATTTTCATAT[-/GA]GTTATACAAGCAAAA | 64326 |
rs148228762 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176129340 | TCAAAAGTGTCATAT[A/G]AAAGTCTTACCTATA | 64326 |
rs148236878 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176076185 | AACTCCTCATCTGTA[A/C]ATGGAACATGTTTTA | 64326 |
rs148239998 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176015672 | CTCAATTCCTGCCTA[A/C]GCTGGATATGACTGC | 64326 |
rs148245659 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176170190 | AAAGTCATCCATGAC[A/G]GCTGGAATCAACTTC | 64326 |
rs148250133 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176178276 | ACCAGGAAATATACA[C/T]ACAAAATTTAACTCT | 64326 |
rs148267654 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176112165 | CTGTCTCAGTGCACT[A/C]TCTCAAACCAAAAGT | 64326 |
rs148290943 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176019909 | CATTTATTTCCAATA[A/T]GATCTATTTATATAT | 64326 |
rs148302012 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176208031 | AGACCCAGCTCAGTC[A/G]GAACCTAGGTTTATT | 64326 |
rs148306527 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175961226 | CCAAATAAAAACCCT[C/G]TCATAGATCTAACTA | 64326 |
rs148320301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176055263 | ACACGATGAAATCCA[A/G]CCTCTACCAAAAATA | 64326 |
rs148323080 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:176032763 | AGAGACATCTACTGG[C/T]CACATAAATGAAGCC | 64326 |
rs148324826 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175971694 | AATGTTTAATGGAAT[G/T]TGGCTGTAAACATCA | 64326 |
rs148333339 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | RFWD2 | GRCh38.p7 | 1:176156588 | ATGACAGAACTAAAG[C/T]ACAAGCATGAAGAAG | 64326 |
rs148371276 | snp | C/T | 0.16618 | 0.23553 | intron-variant | RFWD2 | GRCh38.p7 | 1:176058413 | AGACTTTTCATTTTG[C/T]TCTGTACTAAGAAAA | 64326 |
rs148376111 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | RFWD2 | GRCh38.p7 | 1:175977495 | ATTTTCCTGGAAATA[A/G]CTGATGTCAACCCTG | 64326 |
rs148377413 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176067919 | GTCTGTCCCCTCCCC[A/G]TAGGGTCACAACTCC | 64326 |
rs148385881 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176162344 | ACTTGCAATTTCACA[C/T]TTTACGTCTTTAACA | 64326 |
rs148386876 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | RFWD2 | GRCh38.p7 | 1:176091090 | AAAGGACATCAATAA[A/T]CTTAAAAAAGTTGAG | 64326 |
rs148390774 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176054123 | TCTTACTCTTCACAA[A/C]TTTCCCATACCTTCA | 64326 |
rs148404777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176154337 | TAAAGACATATGCAC[A/G]TGTATGTTCACTGCA | 64326 |
rs148421420 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176190050 | GGTTATTATAGGCAT[C/G]TGACTTTACAACTCC | 64326 |
rs148425100 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | RFWD2 | GRCh38.p7 | 1:176001222 | AGTTATTTCTAAAGA[A/G]AATTAACATCAGAAT | 64326 |
rs148440506 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:176095385 | ATGTTCTTAAAAATA[C/G]TAAGATGTTATTTGC | 64326 |
rs148442194 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176037660 | AGTTTTGAAAGTCAA[C/T]GACTATAATTCATAA | 64326 |
rs148470952 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175945705 | AAGTAAGTTGTGATA[C/T]TGCTAAAACTAAGAG | 64326 |
rs148474848 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | RFWD2 | GRCh38.p7 | 1:176194406 | GCACTTTGGGAGGCC[A/G]AGGCAGGCGGATCAC | 64326 |
rs148485025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175958885 | TACGAGTTCAGCCAA[C/T]ATTCAAGAAAGAAAT | 64326 |
rs148488693 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176125793 | TGATAGTGATTGCAA[C/T]GTATCTGTAGATTGC | 64326 |
rs148493970 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176041171 | TAAATATTTCCAGGA[A/T]AAAAAGGTTATTTGG | 64326 |
rs148548203 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176077761 | GAAAACCCTAAAGAC[C/T]CTGCCAAAAGGCTCC | 64326 |
rs148557947 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176171785 | GTACTACAGGCAGAT[C/T]AGTCAGAATTTCAAG | 64326 |
rs148558055 | in-del | -/CA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176082297 | ATACACACACACACA[-/CA]ACTTTTTCAAGGTAA | 64326 |
rs148562770 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176179669 | TTGAGCCCAGGAGAT[C/G]GAGGGTGCAGTGAGC | 64326 |
rs148600012 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176082040 | GGAATTTAAAACATA[A/G]TATCAGTTTACGAAG | 64326 |
rs148601804 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176021702 | AAGGCCTAGCTGGGA[C/T]CCTTTAACACTACTA | 64326 |
rs148616514 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176116963 | TAGATTTACTTGTTT[A/G]TATTTCATTTTCAGA | 64326 |
rs148633668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176034256 | AAACACTAAGTAAAA[C/T]TGTTGTGTTTATTAA | 64326 |
rs148650322 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176065661 | ACTCCTTTTGGGAAA[A/G]TGTTTCCCCCACTCC | 64326 |
rs148677242 | snp | A/G | 0.472896 | 0.113214 | intron-variant | RFWD2 | GRCh38.p7 | 1:175995874 | tcaacagaaaaagag[A/G]gaatcctccctaact | 64326 |
rs148687344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175979071 | TTTCTTGGTTAGGAT[A/G]TATAACAAACTTCTT | 64326 |
rs148702272 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176070096 | CGAACCCTGTTGCTA[C/T]TTGAACAAGCTCCTC | 64326 |
rs148703688 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176008615 | ATAATTTCTACTAAG[A/C]ATTTTTCTTGTTTGT | 64326 |
rs148704105 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | RFWD2 | GRCh38.p7 | 1:176104140 | CACATAGCTAGTCAT[C/T]TGGATGGATGAAATT | 64326 |
rs148745211 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175956206 | TCCATCCATAATCAA[C/T]TGAATTTCAAAACAA | 64326 |
rs148755887 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176013037 | TTTACAAAGTGACCA[C/T]AGTATATGCTTATAA | 64326 |
rs148757990 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176109663 | ATGGTTACTGGTCTA[A/T]CCCAATTGTCCTAAA | 64326 |
rs148758900 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176050295 | AGCAAGGCAAGAAAC[C/T]GCACAGGACAGCTGA | 64326 |
rs148766622 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176200976 | ACTACAAGCATGCAC[C/T]ATCATGCCCAACTTA | 64326 |
rs148777449 | snp | G/T | 0.0193772 | 0.0965046 | intron-variant | RFWD2 | GRCh38.p7 | 1:175966093 | TGACTTTTCTTTCAG[G/T]ATGTGGTCTTTCAGA | 64326 |
rs148817583 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176206039 | ATAGGTACTTACATT[A/T]TTATAAAAAGCATGT | 64326 |
rs148859282 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176048495 | TACTTGCTGCCATGT[G/T]GATTTTAATGCACCA | 64326 |
rs148861358 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175989310 | ATTACAAGCTGGTAG[A/G]TAAGTACAGAGCTCT | 64326 |
rs148872455 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176146684 | ACTTAATTGCAGCTT[G/T]GTAAGAAACCCAGAG | 64326 |
rs148875563 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176079182 | TCCATAAAGACACAT[A/G]CACTGGTATGTTCAC | 64326 |
rs148882772 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176031951 | ATTGCTTATCTATAA[C/T]AACATCAGATTCAGT | 64326 |
rs148888497 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176181569 | CATTCTTGGCTGGGC[A/G]CAGTGGCTCACGCTT | 64326 |
rs148926108 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | RFWD2 | GRCh38.p7 | 1:176083584 | GTTTGTAAAAGTGTA[C/T]TCAATGTCTCTTTTC | 64326 |
rs148929139 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | RFWD2 | GRCh38.p7 | 1:176119205 | GGACTGAAAGTGAGG[C/T]AATGCAATGCATTAA | 64326 |
rs148934273 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176035951 | GATTAAGTTATAAAT[C/G]AGCAACAGAATGATT | 64326 |
rs148937109 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:176115423 | CCACTGCACTCCAGC[C/G]TGGGCAGGAGCGGGA | 64326 |
rs148941311 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176187803 | AATACACCAAAAAGA[C/G]AAAATACGGGAAAAT | 64326 |
rs148950158 | snp | C/T | 0.000412436 | 0.0143544 | missense | RFWD2 | GRCh38.p7 | 1:176081278 | AACTGGCTTGCAGTT[C/T]GACTGTCATCTATAT | 64326 |
rs148962660 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176131304 | AGGTGATGCTAAGGA[A/T]CTAAACAAGGCAGAA | 64326 |
rs148963268 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176066608 | GCTGCTGACTTTTAC[A/G]TCAAGGTGAGATGGT | 64326 |
rs149001063 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175980581 | ATTTGGAAATCTGTT[A/T]TCCTGATCCCTGCCT | 64326 |
rs149001366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176006377 | TTGTTATGTGTGAAT[C/T]TGATCCTGTCATTAT | 64326 |
rs149014355 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176072659 | TTTTTAAGTATAAAT[G/T]TAAAGCTCACAAGCA | 64326 |
rs149017410 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176009583 | ATGACAGATGTTTCT[A/G]TAGATGTGACAACTT | 64326 |
rs149019265 | snp | C/G/T | 0.00994423 | 0.0699158 | intron-variant | RFWD2 | GRCh38.p7 | 1:175991618 | AATTTTTAAAGCTTT[C/G/T]TGACTCTTGTAATAA | 64326 |
rs149024348 | in-del | -/GAGAGAGA/GAGAGAGAGAGA | 0.493107 | 0.0583 | intron-variant | RFWD2 | GRCh38.p7 | 1:176143123 | TCCAACAGAACAAGC[-/GAGAGAGA/GAGAGAGAGAGA]GAGAGAGAGAGAGAG | 64326 |
rs149028679 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176175015 | AGGATTCCCTATTCA[C/T]GTCTCTCTTCTCTAG | 64326 |
rs149068681 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | RFWD2 | GRCh38.p7 | 1:176015390 | AGTCCAATTAACAAC[A/G]ACAAGGTCTGGTAGA | 64326 |
rs149074995 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176026663 | AGTAGCCCAGTGACA[C/T]AGTGAGTTGAATAAA | 64326 |
rs149076675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175967903 | GATGGAGTCTCGCAC[C/T]GTCACCTAGCCTAGA | 64326 |
rs149083978 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176111718 | GTCTATTTTGTTCAT[A/G]CTTTTGGGTTTTTTT | 64326 |
rs149084940 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176052267 | GCAAGAGGCTATACT[A/G]TATCACCTACATGTC | 64326 |
rs149086959 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176152106 | GACCAGCCTGGGCAA[C/T]ATGGCGACACCCCAT | 64326 |
rs149091286 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | RFWD2 | GRCh38.p7 | 1:176059992 | AAACTGTTTTTTTAA[G/T]AGCAACCTGCTAGAT | 64326 |
rs149141610 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | RFWD2 | GRCh38.p7 | 1:176087445 | AAAAAGTGGGAGAAG[A/G]GTATGAACACACACT | 64326 |
rs149156420 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176191633 | TCTTTACACCTATAC[C/T]GATAACACTAGATCC | 64326 |
rs149157620 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176167953 | GGACTTTTATATGCA[A/T]CAGCCATTTTTTTTT | 64326 |
rs149158391 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176002081 | TAGGTGTACATCTTA[C/T]CTACTTGGGGTTTAT | 64326 |
rs149171881 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | RFWD2 | GRCh38.p7 | 1:176099090 | ACCACAGAGATAATC[A/G]AACTACTTTGTCAAT | 64326 |
rs149173288 | in-del | -/C | 0.040671 | 0.13668 | intron-variant | RFWD2 | GRCh38.p7 | 1:175950889 | GGCTAGTGAAGAAAA[-/C]CTGCATCTACTAAAA | 64326 |
rs149207396 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176195837 | GGAGCTACACACTGG[A/G]TACACACAGACACAA | 64326 |
rs149208922 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176128199 | ACAGTGTTTTATACA[C/T]GCTGGCTCAAATACT | 64326 |
rs149218998 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175959660 | TAAGGACTACCTAGA[A/T]ACCTTTCTCTTATTT | 64326 |
rs149226541 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176102886 | TCAGTGCAAGAGGAC[A/G]GCTTCAATTCCCCAT | 64326 |
rs149253792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176189574 | GCCCACAGACCTGTA[C/T]TACAAGATATATTAA | 64326 |
rs149257323 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | RFWD2 | GRCh38.p7 | 1:176120510 | TAACTAAAACTGATA[C/T]AGGAGTAATACACTT | 64326 |
rs149262829 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:176133142 | TACCCATACACATAC[A/G]TATATACGTACATAT | 64326 |
rs149286712 | in-del | -/A/ACACA/CACACACACA/CACACACACACA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175955766 | CATTTAGAGACAAAC[lengthTooLong]CACACACACACACAC | 64326 |
rs149299376 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176040815 | TGATGCGAAATAAAG[C/T]TTCCAATGCTAGAGC | 64326 |
rs149302439 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175982959 | AGTTTTTGAGATGTA[C/T]TGCATAGCAGAGTGA | 64326 |
rs149315922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176074304 | GTTGAAGTAAATTTA[C/T]TATCAATGATGTGTT | 64326 |
rs149339354 | in-del | -/AG | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176151384 | GAAAGAAAGAAAGAA[-/AG]AAAGAAAGAAAGAAA | 64326 |
rs149341857 | in-del | -/TAAA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176062777 | ATTATTCAAATGAAT[-/TAAA]AAACTGTAGAATATT | 64326 |
rs149368174 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176077263 | GCTTACAAAATACTT[G/T]TAAGCTGAATCCAGG | 64326 |
rs149382724 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176179494 | AATCTCAGCAATTTG[C/T]GAGGGCGAGGCAGGA | 64326 |
rs149392340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175969208 | TTCAATTTCTCCAAA[C/T]ATAAAGCAGATACTC | 64326 |
rs149397976 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | RFWD2 | GRCh38.p7 | 1:176112869 | TGACCTCCAGTTCCA[A/T]CCATGTTGCTGCAAA | 64326 |
rs149403622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176029108 | ATATACATCATAAAT[A/G]TGAAAATGTACACAA | 64326 |
rs149404894 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | RFWD2 | GRCh38.p7 | 1:176124733 | CTGCAACAAACATGG[C/G]AATGCAGATAACTCT | 64326 |
rs149406975 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176061600 | CATTGAACTCCAGCC[G/T]GGGCAGCAAGAGTGA | 64326 |
rs149459843 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176065621 | GCTTTCTGTCCTCCC[C/T]TATTTGCCTGAAAGC | 64326 |
rs149468707 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176158785 | GCTGGGACTATAGGC[A/G]CACACCGCCATACCC | 64326 |
rs149476982 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | RFWD2 | GRCh38.p7 | 1:176100935 | CTAGGAAAGAAAACC[A/G]GATCTGATGGATCCA | 64326 |
rs149489103 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176202482 | GCGTGAACCAAGGTG[A/C]CCACCCTCACTTTTT | 64326 |
rs149495835 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:175957934 | AAAAATTACATACTG[C/T]ATCATTCCTGTTATA | 64326 |
rs149527031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176104113 | ATAAACTTTTTAAAA[C/T]AGGGCTGGGGGCACA | 64326 |
rs149542621 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207706 | CTCTCTCTTCTGAGG[A/G]GTAGGCAGGTGCTTC | 64326 |
rs149547586 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175961153 | ATTCTGCCATGCTAC[C/T]GGCCTCCCTGGCATA | 64326 |
rs149556086 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176143394 | GCAAACAATCACAGG[C/T]CTAGACTGCTTCTCC | 64326 |
rs149560991 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:176055099 | CTGACAACTCCATCA[C/T]AGTCTACTTTGGTCA | 64326 |
rs149609111 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176148342 | AGTAAAAAGTATCCT[A/C]ATTAGACAATTCTTA | 64326 |
rs149609993 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176080922 | TAGACAATGATAGTA[C/T]AAGAAAACAAGCTAC | 64326 |
rs149611252 | in-del | -/AGAA | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176154943 | TAGAAAATTTTAAAT[-/AGAA]AGATTATTAGACATA | 64326 |
rs149615325 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176090930 | ATAATTAAAAAGAAA[A/C]CCACAGTTAGACACA | 64326 |
rs149625802 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176184523 | CAAGAAAAAAAATAT[A/G]ACTGTAACATAATCA | 64326 |
rs149662671 | snp | A/G | 1.73984e-05 | 0.00294939 | intron-variant | RFWD2 | GRCh38.p7 | 1:176085749 | AAATGTAGATTTCAG[A/G]TAATTTGAGAAGGTC | 64326 |
rs149664663 | snp | A/C/T | 0.00874735 | 0.0655527 | intron-variant | RFWD2 | GRCh38.p7 | 1:176025894 | ATAAAAACAAAAAAA[A/C/T]CAAAAAAAAAGAAAA | 64326 |
rs149694709 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176181105 | TTGTATTTCAGTTAG[A/G]CTACAGATACAGGTA | 64326 |
rs149699009 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176113895 | ACTACAGGGAGGCTA[A/C]AGTTTTAACCAGTAA | 64326 |
rs149716384 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:176031540 | TTAAAAGAAAATATC[A/G]TCTTCTAGGTGAAGA | 64326 |
rs149717977 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:175945235 | AAAGGAATTTAATGA[C/T]TCTTTACTATATTTA | 64326 |
rs149718221 | snp | A/C/T | 0.0185938 | 0.0946107 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175970483 | ATTGAAAATCTTGAA[A/C/T]GTAATAGTTTAGATA | 64326 |
rs149729146 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:176125368 | TGTAGTAGTTTCACA[A/G]TTTGAGGCCTTTAAG | 64326 |
rs149732907 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | RFWD2 | GRCh38.p7 | 1:176166570 | TCTACATTTACCAAA[C/T]GAAGTTTTTTACTAC | 64326 |
rs149770135 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RFWD2 | GRCh38.p7 | 1:175973999 | GTAAGAGATTGAGCT[A/G]GAGAGGGAGGTGGGG | 64326 |
rs149775934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175987646 | GCCATCTATTAAAGA[C/T]AGAATAATTGTTCCA | 64326 |
rs149785051 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176066275 | CCCTCACCTCTTCAG[C/T]CCCCATGCCCCATGT | 64326 |
rs149786709 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176171471 | TACTAAACTTTCTCC[A/C]TATCAGCAATAAGCG | 64326 |
rs149786942 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176102165 | CGGGGAGGAGCCTGG[C/T]CTCTCTTGTCCCTGG | 64326 |
rs149803208 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176204185 | GTCCTTACCTGTCCA[A/T]CGACAAACAAAATTA | 64326 |
rs149805161 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:176017346 | TTCTCAGATGCTTGA[A/G]AGTTTATAAAAGTCC | 64326 |
rs149840975 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176105902 | CAAAATTATGACTAA[A/G]ACAGTGAAAGAGATC | 64326 |
rs149841951 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176045844 | GGGGAAAAATTCCTG[A/G]TGTTCAAATACTATT | 64326 |
rs149843047 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176120414 | GCTGGGTGACAGGGC[A/G]AGACTCTATCTCCAA | 64326 |
rs149844281 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | RFWD2 | GRCh38.p7 | 1:176021305 | ACCAGAAGTAAAAGC[A/G]TTAAAAAACACACTC | 64326 |
rs149857919 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176144952 | CTTCATGACCACAGG[C/T]GGAAAAGACTTCTTT | 64326 |
rs149860496 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:175963393 | ACTTTCCCTCATCTG[A/C]GCCTTTGTTTACACT | 64326 |
rs149872968 | snp | A/C | 0.0189856 | 0.0955633 | intron-variant | RFWD2 | GRCh38.p7 | 1:176115949 | ATGGAAAAGCTGTTA[A/C]GTTTCAACGTAATGA | 64326 |
rs149874424 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176056379 | ACTAAGATCTGATTT[A/G]ATTTAAAGTCTCATA | 64326 |
rs149908256 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176151849 | TTCACTATAAATGAG[A/T]AATTTGGTCCTTACA | 64326 |
rs149912477 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant, utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175967609 | ACAGCAAAACACACA[A/T]CAGGAAAAACCAAGA | 64326 |
rs149926508 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176059869 | TGTCACAAAGTATTA[C/T]CCTTTGTATTTTTTT | 64326 |
rs149928694 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:175998871 | AGTGCCTGTTAAGCA[A/G]TAATGGAATGGAACT | 64326 |
rs149936758 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175950433 | GCAACAGAAAAATAA[A/G]ACCAGATATTTTACT | 64326 |
rs149938496 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176186531 | GGTGACAGAGCAAGA[A/C]CCTATCTCAAAAAGA | 64326 |
rs149939672 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | RFWD2 | GRCh38.p7 | 1:176163487 | TGGCCTCCCAAAGTG[C/T]TGGGATTATAGGTGT | 64326 |
rs149944032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176091809 | TGAAATTATATCAGT[A/G]TTAGCAATAAATGTA | 64326 |
rs149955968 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:176196949 | ACCAGCAGGAGGGAG[G/T]GAGGGAGGGAAAGAA | 64326 |
rs149980931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176001985 | ATCTTAATGAGGATC[C/T]CTGGTACTTGCTGAG | 64326 |
rs149983548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176038847 | GAAAAGAAAAAGATA[A/G]ATACACAGATCAATG | 64326 |
rs149988297 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RFWD2 | GRCh38.p7 | 1:175955048 | AGTCCAGGAGTGTGA[A/G]ACCAGCCTGGGCAAT | 64326 |
rs149991220 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176191613 | AATAATAAACCTCAA[A/G]CTCTTCTTTACACCT | 64326 |
rs149993730 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176097608 | GTGCAGCAGCTCAAG[C/T]CTGTAATCCTAGCAC | 64326 |
rs149997065 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176134497 | CAAATATAACCCTAT[A/T]CTAATATCGCATATA | 64326 |
rs150002743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176049782 | TGCAGAAAGCTTTCT[A/G]GAACTAATACAAAAC | 64326 |
rs150008932 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176200711 | AAGAAAAACATGTTA[C/T]TCTCAGTGAATATAT | 64326 |
rs150017639 | snp | G/T | 0.0248432 | 0.108648 | intron-variant | RFWD2 | GRCh38.p7 | 1:175990929 | TTTTTTGTAAACCCA[G/T]TCTGCCAATCCCTGA | 64326 |
rs150020592 | in-del | -/A | 0.0850919 | 0.187897 | intron-variant | RFWD2 | GRCh38.p7 | 1:176192857 | GTTCCTTGTATCCCT[-/A]ACTTTGATTTTTAAG | 64326 |
rs150041404 | snp | C/T | 5.16551e-05 | 0.00508182 | intron-variant, splice-donor-variant | RFWD2 | GRCh38.p7 | 1:176163814 | AAGAGTTGAAACATA[C/T]GGTGCTACTCACTGA | 64326 |
rs150050090 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176141071 | CTGACTTTCATTAGT[C/G]CCTTGATAAAGATAT | 64326 |
rs150051508 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176075812 | GTTCGAGACCAGCCT[C/G]GCCAACATAATGAAA | 64326 |
rs150066171 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176177463 | TTAAAAAATCATATA[C/T]GTGTACATTTAAAAT | 64326 |
rs150066623 | in-del | -/AATA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176062774 | ACAATTATTCAAATG[-/AATA]AATAAACTGTAGAAT | 64326 |
rs150094850 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176133094 | TACTATATATACACA[C/T]ATATACACATATGTA | 64326 |
rs150097092 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176068242 | CTTCTCTCCCTGCCT[A/G]CTTTCTTCCTTTCTT | 64326 |
rs150103125 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | RFWD2 | GRCh38.p7 | 1:176078433 | TGGTGCTTGGATAAC[C/T]AGCTAGCCATGTGCA | 64326 |
rs150106048 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176018144 | TGCACTAATGTTAGC[C/T]ATTATTATTTACCCT | 64326 |
rs150112608 | in-del | -/CTC | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176016553 | GAGGAGCTCTTTCTT[-/CTC]CTTCTCTGTCTCTCT | 64326 |
rs150147152 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175997074 | CAATGGAACAGAACA[C/G]AGTCCTCAGAAATAA | 64326 |
rs150157823 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176022917 | GCACTTATTTAAGAT[C/T]TGAAAGGTGAACATT | 64326 |
rs150159896 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175964992 | GTTAATTTGCACTCA[G/T]ACAAAGATGATTTCA | 64326 |
rs150165529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176108563 | TCTCCCTTCCTCCAC[C/T]TACCCTTCCCCAATA | 64326 |
rs150171064 | snp | C/G | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176119111 | AAAATGTAACCATTA[C/G]TTGCCTTTCCTATAG | 64326 |
rs150187211 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176057383 | TCTCCCTCTGATGCC[A/G]AGCGGAAGCTGAACT | 64326 |
rs150199811 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:176160106 | AATAGGAAAGAATCT[C/G]TAATCTAATAAGACA | 64326 |
rs150211435 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175969178 | AATTTTGGTTCTGCT[G/T]AATCCTTTTAGACAT | 64326 |
rs150225247 | snp | C/T | 0.0718919 | 0.175435 | intron-variant | RFWD2 | GRCh38.p7 | 1:176061494 | CACTAGGCATGGTGG[C/T]GTGCGCCTGTAATCC | 64326 |
rs150240568 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176000385 | GTATGTTCTTGGCAA[C/G]TTTGTCAAAAATGAG | 64326 |
rs150245619 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176009498 | AAATTATGTCCTTGT[A/G]TACTGTACAAAAGTT | 64326 |
rs150248293 | snp | A/C/T | 0.00398635 | 0.0444788 | intron-variant | RFWD2 | GRCh38.p7 | 1:175951992 | GGCACACCACAGTTA[A/C/T]ACTGCTGAAGACAAG | 64326 |
rs150252681 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176165170 | ACAGTACTTGTAATA[C/T]AATGTGATAATCAGT | 64326 |
rs150268706 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176198241 | TTTCAAGATGTACTA[C/T]AATAATACCATAATC | 64326 |
rs150285286 | in-del | -/A | 0.0429648 | 0.14013 | intron-variant | RFWD2 | GRCh38.p7 | 1:176202855 | ATCTGTCATGACACT[-/A]AGAGAGGCAATGATA | 64326 |
rs150299439 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175957564 | GGCATTTCTCAAAAC[A/G]TATCCCCATTGTTAA | 64326 |
rs150301956 | in-del | -/AG | 0.0689305 | 0.172377 | intron-variant | RFWD2 | GRCh38.p7 | 1:176019792 | TTGAGCCTGGAAGGC[-/AG]AGAGGCTGCAGTGAG | 64326 |
rs150306783 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | RFWD2 | GRCh38.p7 | 1:176100699 | TAAGAACAAGGGAGC[C/T]AACCAAAGACAAGAA | 64326 |
rs150308471 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176040206 | ATTTAGAAATTCAAG[A/G]ACAATTTTTCTTTCT | 64326 |
rs150314271 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176051426 | TTGTGGAGAAGATGG[A/T]GTGAACAAACCTACC | 64326 |
rs150315826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175991976 | GAAGTACAGTCTATA[A/G]TAATGGTAAAAAGTA | 64326 |
rs150318719 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176202181 | TATGATACGTTCTAG[C/T]TCACTTTTTTTTTTT | 64326 |
rs150323556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176137027 | TGCTGGTATTACAGG[C/T]GTGAGCCACTGCACC | 64326 |
rs150344279 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176082296 | ACATACACACACACA[C/G]AACTTTTTCAAGGTA | 64326 |
rs150363583 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176076612 | TAGTAGAAGAAAAAA[C/T]TAAAATCAGAGAAGA | 64326 |
rs150367177 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176063071 | TTTTTTTTTTTTTTT[G/T]AGACGGAGTCTCGCT | 64326 |
rs150373671 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | RFWD2 | GRCh38.p7 | 1:176142320 | AGAAAAGCAACAATA[A/C]TAAAAAAAGAAATAT | 64326 |
rs150376318 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | RFWD2 | GRCh38.p7 | 1:176178659 | GAGTTCGAGACCAGC[C/T]TGCCCAACATGGCAA | 64326 |
rs150401542 | in-del | -/GT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175980751 | CTAAAGGAGTAATAA[-/GT]GTCCTTTACAAGTAC | 64326 |
rs150411288 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176123025 | CAGTTCATTACACAA[A/C]GTGGTTTATTTGACT | 64326 |
rs150419802 | snp | C/G | 0.040671 | 0.13668 | intron-variant | RFWD2 | GRCh38.p7 | 1:175995829 | AGGTACAAGGAGGAA[C/G]TGGTATCATTCCTTC | 64326 |
rs150430099 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176183404 | AATTAAAAATACACA[G/T]ATTACACATCCATCA | 64326 |
rs150458063 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175984574 | GGGCACCACCTATGG[A/G]GCTGTGAGAAGAGGG | 64326 |
rs150465684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176127531 | AATGACAGAACTTCC[C/T]GGGTCTTTTTAAGGT | 64326 |
rs150505403 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175977702 | GACAATCTGTATATT[C/T]TTAAATTAGTAAAAA | 64326 |
rs150519190 | in-del | -/AAAAT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176077914 | CAATAGCCACAAAGA[-/AAAAT]AAATAACTAGGAACT | 64326 |
rs150539836 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | RFWD2 | GRCh38.p7 | 1:176062920 | TGTATGGTTCCACTT[A/G]TAAGAAATTTTTAAA | 64326 |
rs150542083 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176001297 | TCGAATGAACCTCTA[A/G]GCATCAAGTATTTGA | 64326 |
rs150552423 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176165969 | CCATTTGAAGAAAAA[C/T]AGTGACTGTTAAATA | 64326 |
rs150557309 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175982646 | GAATCAAATTATACC[C/T]GAATTTTCAACTGAG | 64326 |
rs150570372 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176096028 | CAGGACTCTCTCTTG[C/G]TTTGCTGAGCGTTAT | 64326 |
rs150572379 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | RFWD2 | GRCh38.p7 | 1:176074174 | TCAAGTGATCTGCCT[C/G]CCTCGGCCCCGCAAA | 64326 |
rs150573826 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176010405 | TAAGTTTTTACTAGT[G/T]GGTCACTCATTGTAT | 64326 |
rs150582626 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176200069 | ACTGGTACCACCATT[A/G]TTAACCGTGTAACTG | 64326 |
rs150607135 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:176101417 | TTGGAAAAAAAAAGG[C/T]TTTCTTTTTCCTTTC | 64326 |
rs150622144 | in-del | -/TTAG | 0.105924 | 0.204309 | intron-variant | RFWD2 | GRCh38.p7 | 1:176029253 | ATATTCTAGAATTAT[-/TTAG]TTAAATTGCAAAATT | 64326 |
rs150625073 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176016992 | ATTACAGAATAATTT[C/T]TAGTACAACAAATAA | 64326 |
rs150627871 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175958966 | AATTTGCTTTATGAA[A/G]TTAATATACCCATGA | 64326 |
rs150628186 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176052892 | CATATCAGCACATAT[C/G]AGAGCAACCTCATTT | 64326 |
rs150635724 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176203849 | TACTGAAATTAGGTA[C/T]GTGACTATTTAAATC | 64326 |
rs150636215 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176139567 | CATCAATGCCCATCA[C/T]TGCCCATCAACGGTG | 64326 |
rs150639828 | in-del | -/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176036507 | AAAAAAACAAAAAAA[-/C]AAAAAAAAAAAAAAA | 64326 |
rs150640342 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176112612 | ATATACAATAAAGTA[A/G]TAACTATAATTTCCC | 64326 |
rs150643814 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176153663 | GGGCATCCTTGTCTT[A/G]TGTTGGTTTTCAAGG | 64326 |
rs150678912 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175963240 | CTACAGAAGAAGGTC[C/T]AAACTTTTTTTTTTT | 64326 |
rs150692243 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176056066 | TTTCCATTTTGATCC[C/T]AGCGTTGCCAAAAAA | 64326 |
rs150693438 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176158269 | AACATTTCTTTAAAA[C/G]CCAATCTGGAATTTT | 64326 |
rs150695235 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RFWD2 | GRCh38.p7 | 1:176087752 | CAGCCACCCCATTAC[A/G]GGTTATATACCCAAA | 64326 |
rs150705109 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176179898 | TAGCTGGAAGTAACT[C/G]TCCTCACTAACACTA | 64326 |
rs150708902 | snp | A/T | 0.00318978 | 0.0398085 | downstream-variant-500B | RFWD2 | GRCh38.p7 | 1:175944445 | GCTTATGGTATGTTT[A/T]TGTAACATTTCAAAG | 64326 |
rs150709772 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176192941 | GTGCTGAATTTAAAA[C/T]ATAGTACCAATTAAA | 64326 |
rs150748409 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176091614 | GTTCAGGAAGGTAAT[C/T]AAGATAATTAAGATA | 64326 |
rs150749659 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176034743 | GCAGCAAATGCTTTG[C/T]GCACTGAACTACAGT | 64326 |
rs150763392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176196813 | GAGAGGTCAAAGCAC[A/G]GGAAGATCACTTGAG | 64326 |
rs150764816 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176130068 | TGTTAATCCATATAA[C/T]GTCCACCCAGTTTAC | 64326 |
rs150767645 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | RFWD2 | GRCh38.p7 | 1:175950266 | GTTTGAATGGTCTTT[C/T]AGGACTGAAATTTAA | 64326 |
rs150782230 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176043566 | CAGGAAAAAAAAGCA[C/T]TTGGTATTGCATAGG | 64326 |
rs150817478 | snp | C/T | 0.000771307 | 0.0196229 | intron-variant | RFWD2 | GRCh38.p7 | 1:176133833 | ACAACTTTTTCTTCC[C/T]TGTATGTACTTACAT | 64326 |
rs150831506 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176071157 | ATCCCTCATGGCTTG[A/G]TGCTATCTTCATGAT | 64326 |
rs150836658 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:175990418 | ATATGGTGTCCCCTG[G/T]AGACTGTTACTAACA | 64326 |
rs150840295 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176020449 | TTTGGGAGGCCAAGG[A/C]AGGTGGATCACCTGA | 64326 |
rs150847560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176174048 | CACTTTCCAGCTTAA[A/G]TGGCAGTATATTTTT | 64326 |
rs150850833 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176080064 | CTAGTAACAGCCTCA[C/G]TAATCATGGGTCGAA | 64326 |
rs150853109 | snp | C/G/T | 0.0189856 | 0.0955633 | intron-variant | RFWD2 | GRCh38.p7 | 1:176115700 | GCAGTGAGCCGAGAT[C/G/T]GTACCACTGCACTCC | 64326 |
rs150892942 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176025429 | TACAAAACAAATATC[C/T]AAATATGAACAAGTT | 64326 |
rs150894742 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175966519 | ACACAGCTAAGAAAG[A/G]GCAAAGCCAGGAATC | 64326 |
rs150898659 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176176957 | CCTTAAGGTTTTTAC[A/G]TACCCTTTTGAATAT | 64326 |
rs150908012 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176119892 | AGTGAGAAAATTCAG[A/G]CACTGAGAGATTATA | 64326 |
rs150909457 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176059104 | TCACACAAAAGCACA[A/C]TTTAATGTTTAATTA | 64326 |
rs150918999 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176172013 | CTGAAGTAATCATTT[C/T]TATAATACTCTAGAA | 64326 |
rs150935097 | snp | A/C | 0.0219804 | 0.102504 | missense, utr-variant-5-prime, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176206683 | GAGCTGCTGCCTCCT[A/C]CGCCGGCGCTGGGCC | 64326 |
rs150938826 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176017800 | AAAGTGCTGGGATTA[C/G]AGGTGTGAGCCACTG | 64326 |
rs150941517 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175959877 | ATCAAATACATCTTC[A/G]GGGCTTTCTCAAAAT | 64326 |
rs150946895 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175970030 | TTTTATTCTCACTCA[A/G]TCTTTAACTCCTCTT | 64326 |
rs150954121 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176113647 | ACCAATTAAAAAAAC[A/T]CCTGTAGTTAAATAA | 64326 |
rs150955445 | snp | A/G | 0.021333 | 0.101051 | intron-variant | RFWD2 | GRCh38.p7 | 1:176054307 | GCTGGGATTACAGGC[A/G]TGCACCACCATGCCC | 64326 |
rs150970450 | snp | A/T | 0.0193772 | 0.0965046 | intron-variant | RFWD2 | GRCh38.p7 | 1:176154679 | ACGAAAAATAACTAA[A/T]GGATACTAGGCTTAA | 64326 |
rs151007136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176057213 | CTGCTATGTAGCTCC[A/G]AAATGATTCTAAACA | 64326 |
rs151009993 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | RFWD2 | GRCh38.p7 | 1:175995172 | ACGAAATGAAGGCAG[A/G]AATAAAGATGTTCTT | 64326 |
rs151015234 | snp | A/G | 0.021333 | 0.101051 | intron-variant | RFWD2 | GRCh38.p7 | 1:176004583 | TTGCATTTTGTTGAA[A/G]GCTTTTTCTGCATCT | 64326 |
rs151020387 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:176159905 | CAGATCTAAGACATA[C/T]GCCAAAATCTTCACA | 64326 |
rs151023463 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176194734 | TTAAATATTAAAACA[C/T]GTACATAATAGACAT | 64326 |
rs151026649 | in-del | -/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175962081 | ATGGATAACAAAAGT[-/C]CAGTGACTGCCTTTA | 64326 |
rs151029072 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175946020 | TTGTAGGTATGCTGG[C/T]AATCCCAATTGGTGT | 64326 |
rs151045263 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | RFWD2 | GRCh38.p7 | 1:176041482 | CCACCCTCAGTAGCT[A/C]GGACCACAGGCCTGC | 64326 |
rs151077170 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176197690 | AAATCCATTAACGTA[C/T]GTTCTTTAAATAGGG | 64326 |
rs151078581 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176132042 | GATCTGCTACTTTAT[C/T]TTACAATACAACCAC | 64326 |
rs151083185 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175951708 | AGATGAGACAAGTGA[A/G]GAATAAAACATCAAA | 64326 |
rs151098190 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | RFWD2 | GRCh38.p7 | 1:176044849 | TTGCACATTTTTACA[C/T]ATACAAATACAGAAC | 64326 |
rs151112372 | snp | A/G | 0.0170251 | 0.090679 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176144726 | GAAACAGACCCACAC[A/G]TACATGGACACATGA | 64326 |
rs151119113 | in-del | -/TGAGTCATGGCATTACTG | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175977020 | TCTCTGGAAATCATT[-/TGAGTCATGGCATTACTG]TCACAAAGATATGTT | 64326 |
rs151119881 | in-del | -/A | 0.0158469 | 0.0875917 | intron-variant | RFWD2 | GRCh38.p7 | 1:175962798 | ATCTCCTTTAATCCT[-/A]ATCTCTTAACAAAAC | 64326 |
rs151132970 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176135917 | CTTAAACATGTTCTA[C/T]GTATCAGCAAAAAAA | 64326 |
rs151149181 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176175407 | TCTTCCAGACTGAAG[A/G]GAGGTGGAAGGGATG | 64326 |
rs151152536 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175991665 | CATACATTGTACAGC[C/T]GGACAAAAGTATTTC | 64326 |
rs151157847 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | RFWD2 | GRCh38.p7 | 1:175998428 | TAACTAACCTGCACA[A/T]TGTGCACATGTACCC | 64326 |
rs151167132 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176082086 | CGAATCTATTCTCCA[A/G]TCTATTAATAGAAGC | 64326 |
rs151172381 | in-del | -/TG | 0.0383715 | 0.133092 | intron-variant | RFWD2 | GRCh38.p7 | 1:176127676 | GATAAATACTTAGGT[-/TG]TGTTTGCATGGCTAC | 64326 |
rs151225639 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176038687 | GCCACGTGTGGTGGC[A/G]TGCGCCTGTAATCCC | 64326 |
rs151228289 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175979697 | AGGGGCAAAATGGTA[A/T]TTTTGAAGTAATTAT | 64326 |
rs151228500 | snp | A/G | 0.00841325 | 0.0643105 | synonymous-codon, utr-variant-5-prime | RFWD2 | GRCh38.p7 | 1:176206628 | CCCGTTGCAGAGGGG[A/G]GCGAGGAGAGGTCGC | 64326 |
rs151263930 | snp | A/T | 0.0314385 | 0.121371 | intron-variant | RFWD2 | GRCh38.p7 | 1:175996231 | ctcaataaattaggt[A/T]ttgatgggatatatc | 64326 |
rs151279723 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | RFWD2 | GRCh38.p7 | 1:175983784 | ATGGAGATGAGGAAC[A/T]TGCTGGGAAATAGAG | 64326 |
rs151293159 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176075643 | TATACACACCCAACA[C/T]TGGAGCACCCAGATT | 64326 |
rs151309016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176013495 | GAGCAAACCTACTTG[A/G]TTCTCCTTCCTGCTA | 64326 |
rs151321930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176110430 | CACCTCAGGGATTAT[C/T]TACTTCTTGTTCTCT | 64326 |
rs180671849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176103142 | CATTAGGGTGTTACA[A/G]TTCCTCACACACAGT | 64326 |
rs180687754 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176084747 | TAATCGTGAGGCAAA[C/T]TTGTCTGTAGGATCT | 64326 |
rs180692218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176064994 | TACCTATTGCAATTA[C/T]TCTCCCCTTTATAAT | 64326 |
rs180698307 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176154183 | CCAGCTTTTCTTTGT[A/G]TATCTGGCAGGGCTA | 64326 |
rs180711341 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176134506 | CCCTATACTAATATC[A/G]CATATAGAAGAATTA | 64326 |
rs180712990 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176187771 | ATGCCTGGCACACAA[C/T]ATTCACTGAGTGGCA | 64326 |
rs180717980 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176120672 | GTATAACTATTTTCA[A/C]CTAGATTATTTTCCT | 64326 |
rs180718790 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176171516 | TCATTCGTGTCTTCA[C/T]TGGAGTAGCACTTTT | 64326 |
rs180721467 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176205509 | TCTGAATCAACTTCC[C/T]TCATAATGACTGTGC | 64326 |
rs180751823 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176196744 | TTCCATATCGTCTTT[C/T]AGAAGCCAGCACTGG | 64326 |
rs180762624 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176181638 | ACAAGGTCACGAGAT[C/T]GAGACCATCCTGGCT | 64326 |
rs180781009 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175969269 | AAACACAGTAGAGCA[C/T]TGTTAGGGACCAGAA | 64326 |
rs180790005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175959417 | GCCAGATACCATTAC[C/T]TTTATTTAACATTAC | 64326 |
rs180814338 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175989124 | AGATAAGGGGGGAGG[G/T]TATATAAAAAACTAG | 64326 |
rs180840572 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175944930 | ACCAAGAGCAGCAAT[A/G]TCCATGGAGTTACAT | 64326 |
rs180841944 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176035349 | GAACAATATAAATTA[A/C]CCAACCTGAAGAGAA | 64326 |
rs180844607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176008889 | AGGAGTTGTTCCTGG[A/G]TCAGCAACACTTAGC | 64326 |
rs180849157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176016623 | ATTTAAAATGCAGAC[A/G]GAACAGAGATGCCAG | 64326 |
rs180850637 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:176026277 | TGGCCAGTATGTTTA[C/T]AAAACAGAACATACA | 64326 |
rs180857049 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176001365 | TCTAAGGATCTGACA[C/T]TTTCAGCGATTGAGT | 64326 |
rs180867344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175979823 | AAGTATCTCCCAACT[C/T]CACTTCAGCATTTCT | 64326 |
rs180867842 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992709 | AGGGGCACCTGCCAT[G/T]GCCCAGGCTTGCTTA | 64326 |
rs180873548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176074769 | TCTTCCCCAAAATCA[A/G]GCTAAAATGGCTTTC | 64326 |
rs180873690 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175995059 | TCTCTCAGACCACAG[C/T]GCAATCAAACTAGAA | 64326 |
rs180875471 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176052536 | ATTCTCCCCATTTAC[A/T]ACTATGTAAAATTCA | 64326 |
rs180880046 | snp | A/G | 0.000182193 | 0.00954271 | intron-variant | RFWD2 | GRCh38.p7 | 1:176043673 | TAACAAACCAAATGT[A/G]TGATTCATATAACAT | 64326 |
rs180885273 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176048238 | GGGTCTCACTATGTC[A/G]CCTGGGCTGGTCTTG | 64326 |
rs180895672 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:175953229 | AGAAACCATTAAAAA[A/C]TACAAGAAACAGTAT | 64326 |
rs180896946 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176060191 | AAAAAATTTACTTTC[G/T]TATTCCCTCTGGCTA | 64326 |
rs180901821 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176011466 | CTTAAGATGGTTATG[G/T]TCACATTCACTAATT | 64326 |
rs180905294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175963572 | ATATGCCTTAAAAGA[C/T]TGATGATGATGATTT | 64326 |
rs180905672 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176040725 | CTCTTGTTTGTTTCC[A/C]TTTTTACAGAATAGA | 64326 |
rs180910265 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175984305 | TAAAAGGGGCCAACA[A/G]AGAACTCGAGCCATG | 64326 |
rs180914130 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176022372 | ACTAATTTTCTACCT[C/G]TCAAAACTCCAAAAG | 64326 |
rs180915061 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | RFWD2 | GRCh38.p7 | 1:175997585 | CATGAAAAAGTGGGC[A/G]AAGGGAATGAACAGA | 64326 |
rs180924039 | snp | C/T | 0.0011878 | 0.0243411 | intron-variant | RFWD2 | GRCh38.p7 | 1:176116598 | ATACTCATGGTATCA[C/T]TAAAGCAAACAAAGA | 64326 |
rs180931254 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176097432 | CTGTCTCTTAAAGGC[A/T]CCACCTGGAGACCAT | 64326 |
rs180931587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176079916 | TAGTCCCAGCTACTC[A/G]GGAAGCTGAGGCATG | 64326 |
rs180933287 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | RFWD2 | GRCh38.p7 | 1:176087487 | GACATTTATGCAGCC[A/G]ACAGACACATGAAAA | 64326 |
rs180940792 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176030805 | AAAAGACATGTTTCA[G/T]TCCTAACCCCAGGTA | 64326 |
rs180954365 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:175974966 | GAAAACCCCCCAAAA[C/T]TGCATAATTCAAATG | 64326 |
rs180954988 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176123566 | ATGGAATTAACAGGG[A/T]ATGGCTGGTATATAC | 64326 |
rs180969749 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176106173 | GTAGCTGGGATTACA[C/G]GCATACATCACCACA | 64326 |
rs180978076 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | RFWD2 | GRCh38.p7 | 1:176070184 | ACCAAAACCTTAGAA[A/G]TTATTTCCCTCTGCT | 64326 |
rs181079622 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175971362 | AACTTAATCAGATAA[A/T]ATTTATTCATTTAGC | 64326 |
rs181118019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176129634 | GGATCTTATAAAGCA[C/T]ACCCAGCTGAAGGAG | 64326 |
rs181128120 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176149397 | CAACTAAGAAAACAT[C/G]AAAACAAAATTTACA | 64326 |
rs181140270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175978868 | ATAAGAAACACCTTT[A/G]TAAGTGTGGAAAGTT | 64326 |
rs181148927 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | RFWD2 | GRCh38.p7 | 1:175994832 | TCAACATTAGACAGA[C/T]CAATGAGACAGAAAG | 64326 |
rs181169815 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176008176 | TTGCGCTTCCCAAGT[A/G]AGGCAATGCCTCGCC | 64326 |
rs181179412 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:175958711 | AACTGAAAAGACTTT[A/C]TGTTAATAAATTTTA | 64326 |
rs181220241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176167360 | GATCAGTGTCTGTCT[C/T]GTCCACCATCGTGGT | 64326 |
rs181220975 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176184820 | AAGTCTATAAACATT[C/T]TATCAATAAGAGATG | 64326 |
rs181246355 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176201949 | TCCAGTAACTGAACA[G/T]GCTTTTAACAGCTCT | 64326 |
rs181276382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176064227 | CCAATGTAAAGTTTG[A/G]AAACTTACAATTCCA | 64326 |
rs181278533 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176018302 | GTAATTTAAAATAAT[G/T]AAGACAATTTTTAAA | 64326 |
rs181285545 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176195954 | ACTACTTGGGTGACA[A/C]GATCACTAGCATCAC | 64326 |
rs181291930 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176042791 | GCACTTTGAGAGGCC[A/G]AGGCAGCAAGGCAGA | 64326 |
rs181300520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175990959 | AATGTTACAACATTC[A/G]ACATACTTACATTTA | 64326 |
rs181303283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176101802 | CGAAGCCTCAGATGA[C/T]GGCCCCTTTTGATGG | 64326 |
rs181303540 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176119478 | GTTGAAGATAAAACT[A/G]AGAATTAAAAATAGT | 64326 |
rs181306370 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176002312 | TAATCACAACTGACC[G/T]ATCTCCAAGTTTACT | 64326 |
rs181315803 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176084207 | ATGCAGGTATTGGGC[G/T]ACTTTCAACTTAACA | 64326 |
rs181317654 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176153751 | GCCCTTATTATTTTG[C/T]GGTATGTTCCTTCAA | 64326 |
rs181328482 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176133789 | AGACAATGGGAATGA[A/C]TCATTATTAGTGAAC | 64326 |
rs181399156 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176076276 | ACACCAAGCATAACT[C/G]TTGGACCACAGTGAA | 64326 |
rs181427546 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:176112281 | TTCAAGTTTTTTTTT[A/T]AAATCTTGATTCAAG | 64326 |
rs181428765 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176181528 | TATTCTACTAAAACC[C/T]GCTCTCCAGTGGGTA | 64326 |
rs181435285 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176170648 | TGCAGAGCACAGACA[C/T]GGTAGATTTAGCATA | 64326 |
rs181442233 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176071538 | TGATTTTGAAAAAAA[A/T]TAAGCATAAAAATAT | 64326 |
rs181444372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176088501 | TTGTGGGATCACATG[C/T]ATGTGTTTGTCAAAT | 64326 |
rs181458880 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176124546 | TCTGTTCCTAGCTTA[A/T]TTCACTTAACATAAT | 64326 |
rs181460197 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175952601 | AATATTATACTACAT[G/T]AAAACTCTGATCTAA | 64326 |
rs181463293 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176145063 | ACACCATTAAGATAA[C/T]GAAAAGAATGCAACC | 64326 |
rs181470242 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176108468 | TTTGTGTATAATTAC[A/C]AAATCAAACTATTTT | 64326 |
rs181471387 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175974021 | GAGGTGGGGGCCTGA[C/T]AAAGAAGGTTGTTAG | 64326 |
rs181478113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176129194 | TTAATGTTAAATACT[C/T]TTAGCCTCCATAAAA | 64326 |
rs181480874 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176097214 | TTTTTCTCTTCTAGG[A/T]CCTTGTTTTGTTGAA | 64326 |
rs181483648 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176200428 | CCCATCTGTGAATTA[A/G]TACTAAAGACAGAGG | 64326 |
rs181494620 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176192863 | TTGTATCCCTACTTT[A/G]ATTTTTAAGATTAAT | 64326 |
rs181497795 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176158505 | TTGCTAGAAATCTCC[A/G]TAATTTAACCACAAT | 64326 |
rs181503540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176022030 | CTGAAATTTGAATTA[C/T]CTTAGCATTTTCATT | 64326 |
rs181508483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176166254 | ATCTCAGCCTTCCCA[A/G]TAGCTAGGACTACAG | 64326 |
rs181514804 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176006035 | GTCTGGGTGCCCTTG[C/T]ATTGGGTGCATATAT | 64326 |
rs181520908 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176025120 | GGTACTTGATAAAAT[A/G]CTGTTTTGCTTCTAA | 64326 |
rs181542384 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176054299 | CCCAAGTAGCTGGGA[C/T]TACAGGCGTGCACCA | 64326 |
rs181543452 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992417 | GTGGGTGCAGCGCAC[C/T]GTGCGCGAGCCAAAG | 64326 |
rs181552096 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:176039710 | CCTTACAGTGTGGTA[C/T]TGACATATAAACCAA | 64326 |
rs181562609 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176126849 | AGAACCCAAGGATAT[C/T]TTATAGAAATCCTGA | 64326 |
rs181570906 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176092727 | CAAGAATGCTGAGAA[A/C]CTGGAACTCATACAC | 64326 |
rs181586861 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176186620 | TAAGTTGAGTAAAAC[A/G]GTAATTCACTGGTGG | 64326 |
rs181601578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176163541 | GAAAATATCTAACCA[C/T]TGTTTCACCACCCAA | 64326 |
rs181608062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176115958 | CTGTTAAGTTTCAAC[A/G]TAATGAAGCGTAATT | 64326 |
rs181620908 | snp | A/G | 0.021333 | 0.101051 | intron-variant | RFWD2 | GRCh38.p7 | 1:176049041 | GCCAGGCGCGGTGGC[A/G]GGCGCCTGTAGTCCC | 64326 |
rs181635144 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176184336 | CTTCATGGTTGGTCC[A/T]GATTGTCCAGCATCA | 64326 |
rs181638299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176148774 | TTTTTAGGTAAGTTA[C/T]TGCAGTCAATCTTAC | 64326 |
rs181647636 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176091778 | GAAAAACAGAAGTAT[A/C]ATAAGTAAAACAGAA | 64326 |
rs181663446 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176126620 | CGCCACCATGCCCAG[A/C]CTTCTGTATTTTTAG | 64326 |
rs181666198 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176085552 | TTTAACTTTATCTAG[C/G]TTGCCATATAAAGAT | 64326 |
rs181677895 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176111790 | ACTCGACTATCCACT[A/G]TTTCAATTGTTTTTG | 64326 |
rs181679344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176066586 | GTTATTTACTGGCAG[C/T]CCAGTGGCTGCTGAC | 64326 |
rs181680067 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175957643 | TCTTATAAGGCTAAA[C/G]TTACAACTACTCTAC | 64326 |
rs181708243 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176031947 | AGATATTGCTTATCT[A/G]TAATAACATCAGATT | 64326 |
rs181711713 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176059723 | CCTGACCTCGTGATC[C/T]ACCTGCCTCAGCCTC | 64326 |
rs181743831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175945582 | TAATGATCAAGGTTA[C/T]AGGACCTAAAGTCTT | 64326 |
rs181751350 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176016742 | TGACTCTTTTTTTAA[A/C]AAAAAAAATTACAGG | 64326 |
rs181761493 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | RFWD2 | GRCh38.p7 | 1:175989566 | TTGGTTTTTTCATTA[A/G]AAGTTTCACATATGA | 64326 |
rs181789769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176053605 | TGACCACACCCTAAA[C/T]ACTTTTTCATTACCA | 64326 |
rs181790475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175952032 | AAATCTGTAGAAATG[C/T]CAAAGAAACAAAGAC | 64326 |
rs181820596 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175984482 | TGCTGCAAGGGTGGG[C/G]CCCTCATGGAGAACC | 64326 |
rs181826142 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | RFWD2 | GRCh38.p7 | 1:175997712 | AGATACCATCTCACA[A/C]CAGTTAGAATGGCAA | 64326 |
rs181839495 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176079619 | ACAAACCTGCTTATG[G/T]ACCCTTTAATCTATA | 64326 |
rs181843878 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | RFWD2 | GRCh38.p7 | 1:176162463 | CTACTACTGCTACCA[A/G]TGGACACCTGCTGAA | 64326 |
rs181859767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176144340 | AAAGTTAGAGACACA[A/G]ACATCATTTACAATA | 64326 |
rs181863097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176180663 | CTACTATGTATATAC[C/T]TGCTAACAAATATAA | 64326 |
rs181865309 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176013316 | ATACGGTTCAGAAAT[G/T]TACTTAGCTAGGGGG | 64326 |
rs181876820 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176185055 | TGTACTCAAAAGCGT[G/T]TACCGAGACCTGCTA | 64326 |
rs181877866 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176194893 | TCAGCCTGAGCACCA[C/T]GGCGAGACCCTGTCT | 64326 |
rs181887956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176168217 | TGCGCACCACCACAC[C/T]TGGCTAATTTTTTGT | 64326 |
rs181895304 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176202856 | TCTGTCATGACACTA[A/G]GAGAGGCAATGATAC | 64326 |
rs181927581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176002045 | TCTTCCCGCCTTTCA[A/G]GAGTTTCAATATGAT | 64326 |
rs181966928 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176035739 | AAAAAAAAACGCAAG[A/C]ATACAGAAAATCAGA | 64326 |
rs181987527 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175973791 | TACAAAACTCAGCAT[C/T]GTGCAAAGTTCCAGT | 64326 |
rs181990575 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176005998 | AAGTCTCTTTGTAGG[C/T]CACTCAGGACTTGCT | 64326 |
rs181999848 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176048938 | AGCACTTTGGGAGGC[C/T]GAGGCGGGTGGATCA | 64326 |
rs182006776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176154506 | TAAATGAAGCCAGAA[A/G]CCATTATCCTTAGCA | 64326 |
rs182007547 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176031112 | GAGAGTGTGGCCCTG[A/C]CAACAATCTAATTTT | 64326 |
rs182012778 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175970175 | ATTCAAGATGAATGT[C/G]AACATCAGTTGGTAG | 64326 |
rs182013590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176012385 | CTCACCTTGACCTCC[C/T]AAAGTGCTGGGATTA | 64326 |
rs182018484 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176121711 | AATTAAAATGAAATC[C/T]TCTCTCATTGCCTGT | 64326 |
rs182020588 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176087873 | ATGTCCATCAATGAT[A/T]GACTGGATTAAGAAA | 64326 |
rs182023778 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176149769 | TATCATTTACTGTTA[A/C]AATTCACAAGAACCA | 64326 |
rs182033495 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | RFWD2 | GRCh38.p7 | 1:176070636 | CACTGCACTCCAGCC[C/T]GAGCAACAGAGCAAG | 64326 |
rs182035936 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176130054 | CTAAAATCCACATTT[A/G]TTAATCCATATAACG | 64326 |
rs182038080 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176075563 | GATACAGCCCTGTGG[A/T]TTAACAATGTCCATT | 64326 |
rs182041724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176188688 | CTTTGATGTTACTAC[C/T]GTAACTGTTTTGGGG | 64326 |
rs182047228 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176076811 | CAATACCACAGAAAT[A/T]CAAAAGATTCTCAGA | 64326 |
rs182052600 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176054570 | AGTATTTATACCAAC[A/G]TATTTTGATATATTC | 64326 |
rs182052733 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176010254 | AAACTTCAGCCTCTA[A/C/T]CTTCTACAAACAAAA | 64326 |
rs182057061 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176037009 | ATAAGTTTATTAGTT[C/T]GAAATCTACTAAGGA | 64326 |
rs182064463 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176103999 | AAAGAGAAGCTAAGA[C/T]AGGGGAAGAAGAGAA | 64326 |
rs182064621 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176113304 | TGATGGTTAGTGATA[A/C]GTATTTTTACATATA | 64326 |
rs182066703 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175996062 | CCATGATCAAGTGGG[C/T]TTCATCCCTGGGATG | 64326 |
rs182079236 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176092993 | TAGTAACACAATGGA[A/G]TATTATACGTCAGTG | 64326 |
rs182095327 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176127252 | AAAACATACAATTTA[C/T]TATTATTAATTATAA | 64326 |
rs182132966 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176209200 | CAGTGTTTTAAAAAA[C/T]ATATTAGTGACTACC | 64326 |
rs182171077 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176173279 | TCATGCCATTGCACT[A/C]CAGCCTGGGTGACAG | 64326 |
rs182172756 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176156223 | ATATTGTCCTTGAAG[C/T]AGCATACTATAAACT | 64326 |
rs182176819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175960692 | AAATGGTCAAGTTTG[C/T]ATTATAAAGGGCCTT | 64326 |
rs182180750 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175982011 | GGGGTGTGTTAAAAA[A/C]AGATGAAAGATAACA | 64326 |
rs182183599 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176019042 | ATGGTGGTACACACC[C/T]GTGGTCCCAGCTACT | 64326 |
rs182217729 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175966117 | TTTCAGAGTTGACTT[C/G]GTAAAAATATATATA | 64326 |
rs182220908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175986802 | TACCTAAAATGCCTA[C/T]TGTCTTTGGTGACAC | 64326 |
rs182240441 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175964769 | ACAGAACAGTGAGAA[A/C]CATGGCTGAATTTAA | 64326 |
rs182251848 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176013803 | TGCAGAAAAAATTAA[A/C]ATTCCAGACTTATTT | 64326 |
rs182268640 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175999830 | GATAATATCTCATTG[C/T]AGCCATGATTTGCAT | 64326 |
rs182272117 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176021450 | TGCTTCAATCCTCAT[G/T]GATTTGCTTTACATT | 64326 |
rs182283667 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992281 | GGCAAGATGGCCAAA[C/T]AGGAACAGCTCCAGT | 64326 |
rs182285116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176135378 | GATAAATGTAAATGT[A/G]AATATTTTAAATGAC | 64326 |
rs182289580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176137902 | AGGATCGAAAAACAA[C/T]TGTAGCCCTTACCCT | 64326 |
rs182304559 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176107878 | TTAAGCATAAGGAAA[A/C]ACAAGACAAATTCAA | 64326 |
rs182312904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176172260 | TTGCGCAGACTGGTC[A/G]CAAACTCATGGCCTC | 64326 |
rs182317585 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176176317 | ACCAGAAAAGCTAAT[G/T]CCTACAGCTCAGTTA | 64326 |
rs182343089 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176028104 | GTATGGGGGAAACCA[C/T]CTGCTATGATTCAAT | 64326 |
rs182354218 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176206382 | CTGCCTCGCTACTCC[A/C]ACATTCCTTCACCCC | 64326 |
rs182362506 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176042235 | GAGATTGCGCCACTG[C/T]ACTCCAGCCTGGGCG | 64326 |
rs182381848 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176067319 | AAGGTGAGGACAAGC[A/G]TTTCTGTTTTTGTGC | 64326 |
rs182387819 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176208013 | AACAGATTTTGCTCA[A/G]TCAGACCCAGCTCAG | 64326 |
rs182396779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176190168 | AGAAGTGTTTCAGAT[C/T]CGGATCTGTCTGCAT | 64326 |
rs182412942 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175946981 | GACCATCTATTAATC[C/T]ATCCAGCATCCATAC | 64326 |
rs182439760 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176164476 | AATCTAGTCATTCAT[A/G]CCCTTGCCAGTGGTT | 64326 |
rs182446333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176105324 | TAGAAGTAAATGAAC[C/T]TAACTGTATTTCAAA | 64326 |
rs182458524 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176136142 | ACTCCTAGAAATGCA[C/G]AGAGTAGGTATGTAA | 64326 |
rs182563745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176198891 | AAAACTACATATCCA[C/T]AAAAATGACTAATAT | 64326 |
rs182573723 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:175972292 | AAAATACTAATACAC[A/G]TGTTGAAACTATCTA | 64326 |
rs182575437 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176124118 | TTTTTAATTTTTTTA[A/G]ATTTTTAGTGTTTCT | 64326 |
rs182592796 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176158061 | CTACAGATCTAAAAA[A/C]TTCAAAGAACCCAAT | 64326 |
rs182594197 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176192278 | ACCAAGGGTTTACAG[G/T]TAACAGAAGATTTAA | 64326 |
rs182595045 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176081858 | TAAAAAACAAACAAA[A/G]AAAGTTTGAAATTGC | 64326 |
rs182596666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176062339 | TACTGGCCAAAAGAT[C/T]TGAATAGACAATTCA | 64326 |
rs182611494 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176131143 | ACAATAGGCTGGGGC[A/T]AGGCAATTACGGAGG | 64326 |
rs182622841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176099833 | TCACCTTCTACAGGC[C/T]CAGAGCTCCAAGTTT | 64326 |
rs182624211 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176177381 | AAAGAAAAAAATGTT[A/G]TTATACATACTGCTG | 64326 |
rs182629260 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176118068 | AGCATGGGAGGTACT[C/T]TAAGTAGTACACAGT | 64326 |
rs182631305 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176168695 | AGGATCAGGAGAGGG[A/C]AAGAGAGCATTCAAA | 64326 |
rs182639639 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176193440 | CCAGAGACTAGAAAC[A/G]TGTGTTAAAACAAAA | 64326 |
rs182641146 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176086601 | GTTACTTTTTCCAAC[A/G]AAATAAGAGGACACA | 64326 |
rs182649287 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | RFWD2 | GRCh38.p7 | 1:176045815 | TTCTAATATGTTGAG[A/C]TATGTGCAGGCTAGG | 64326 |
rs182650333 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | RFWD2 | GRCh38.p7 | 1:176150973 | TTATAAAAAAGAGAT[A/G]GTGGAAGAAAAGAGA | 64326 |
rs182655829 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:176023770 | GAAAAAGTAAACACA[C/T]TGAATTAGGAATTTA | 64326 |
rs182656258 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176049597 | CAAACCACCTTTTTT[A/G]GTGGAAGAACTTCCA | 64326 |
rs182659591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176122623 | AAAAAAACTTCCCCA[A/G]CACCTCTTGTCTTCT | 64326 |
rs182666811 | snp | A/C | 0.0263992 | 0.111815 | intron-variant | RFWD2 | GRCh38.p7 | 1:175993658 | AGTGATGGAAGATGA[A/C]ATGAATGAAATGAAG | 64326 |
rs182684434 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176145829 | AAGAAAGGCAAGAAA[A/G]TGACTGCCATAATTA | 64326 |
rs182693438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176155629 | TGTTCGCTGCCAAAA[A/G]ACAAAATAAAATAAA | 64326 |
rs182698121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176172747 | CATTTTTTAGTATAG[A/G]AAAAAACAAGTGATA | 64326 |
rs182762776 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RFWD2 | GRCh38.p7 | 1:176109068 | AGTGAGCTGAGATCA[C/T]GTCACTGCACTCCAG | 64326 |
rs182782151 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176159508 | ACCCTAATGCGAGCA[C/T]AAGGAGAAAGGTATA | 64326 |
rs182787552 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175991418 | CATACAGGGGACTTA[C/T]GATGAATGGAGTTTG | 64326 |
rs182790731 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176125524 | CAACTTTGTCAAAAA[C/T]GAGTTCACTGTAGGT | 64326 |
rs182794141 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176141454 | TGCAGTGAGGCGAGA[C/T]AGTGCCACTGCACTC | 64326 |
rs182817061 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176086382 | AGCCGCCCGCCACCA[C/T]GCCCAGCTAATTATA | 64326 |
rs182820091 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176066987 | CATGCAACCCACTCA[C/T]ATGACAACTTATTGG | 64326 |
rs182835202 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176135838 | GGTAAGTGACATAAA[C/T]GTGTAACAACTTAAG | 64326 |
rs182842284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175947757 | ATAAAAGAATAAAGT[C/T]AGAAGCAGAGTAGGA | 64326 |
rs182843298 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:176104265 | CAAGGGGTTTCTCTA[C/T]ATCCTGGTTGTAGGG | 64326 |
rs182848357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176122089 | GGCTTGAAGTAAGCC[A/G]AGATCGCGCCACTGC | 64326 |
rs182849548 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176056179 | AATGTTAATTTTTAT[C/T]TTCTGTAATTTGAGA | 64326 |
rs182854431 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176041687 | AAATAAACAGTAGGC[C/T]GGGCATGGTGGCTCA | 64326 |
rs182864237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176023358 | ACAATACAGGAATTA[C/T]AAAGGAATGTTATTA | 64326 |
rs182873158 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176007384 | TTGTTCCGTTGCTGG[G/T]GAGGAACTGCGTTCC | 64326 |
rs182882542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176124766 | CATGTATACGTTTCC[C/T]TTCTTTTGGATATAT | 64326 |
rs182894925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176061126 | CATACAGATCAATAC[A/G]ACAGAACAGACAGTT | 64326 |
rs182901458 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176089072 | CTTTGGGAGGCCGAG[A/G]TGTGTGGATCACGAG | 64326 |
rs182936166 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176072362 | ACAGACATAGGAATA[G/T]GCAAGAAATAAGACA | 64326 |
rs182937822 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176159187 | TATACAAAATACAAG[C/T]ACACACACATACACA | 64326 |
rs182963313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176185947 | ATAAACACTATCCCT[C/T]AGAATACAGGAATGT | 64326 |
rs182976317 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176179016 | AAAGACAAGGCCGGG[A/T]GCAGCGGCTCACGCC | 64326 |
rs182991686 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176194159 | ACAATCATTAATAAG[A/C]AAATAGTGGAAATAA | 64326 |
rs182995775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175955300 | ATGCACTTGAGAGCA[C/T]TCATCATCCCTTCAG | 64326 |
rs183002732 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175976244 | AATGCAAATACCCAT[A/G]TAAGTCTCTATATCA | 64326 |
rs183008528 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176147483 | ACCAAAATGTATTAA[C/T]GACAGTACAATCACT | 64326 |
rs183012269 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175993541 | AACCAATACAGAGAA[G/T]TGCTTAAAGGAGCTG | 64326 |
rs183019925 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176114863 | ATACTTTATCAATAT[A/T]AACTGCTTGAATTTT | 64326 |
rs183032301 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176182795 | ATGTCCAGAATGTCA[C/T]TGGCAATACAGAGCA | 64326 |
rs183039342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175959771 | AAAACTGAGTGTCTC[C/T]CATCTCCCTAGAGAG | 64326 |
rs183042037 | snp | C/T | 0.00478085 | 0.0486577 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207599 | CACCCAGGGTATCCG[C/T]CCCAAGCGGAGAATA | 64326 |
rs183047470 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175980063 | TGCATCACCACATTT[C/T]AACATTATAACAACC | 64326 |
rs183050375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175948592 | ACATATGCAAGTTGC[A/G]CTTTACAAACTCATA | 64326 |
rs183055299 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:175995096 | ATTAAGAAACTCACT[A/C]AAAACCGCTCAACTA | 64326 |
rs183077645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176044070 | AGATGGATGTGAGCC[C/T]AGAGCTATCACTGGC | 64326 |
rs183087358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176027330 | ATGCATATAAACACT[A/G]AGAAAAATGACAAAA | 64326 |
rs183094881 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176009259 | AATACTGTGGGTATC[A/G/T]ACAGGTATTTTCCCA | 64326 |
rs183098140 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175972715 | AGGTGATCTGCCCGC[C/G]TCGACCTCCCAAAAT | 64326 |
rs183142683 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176009542 | AAATTGCGTACTGCA[C/T]GAAGGTTTTTACAGT | 64326 |
rs183145768 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175980933 | CCCTTTACACAGGCA[A/T]CATCACATAGGAACA | 64326 |
rs183160346 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176114259 | TCTGGTATTTTCATG[A/T]CCGTTCAGAAACAGA | 64326 |
rs183176041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176146548 | GCTGCCATGTAGTGA[A/G]CTATCCTATGGAGAA | 64326 |
rs183184033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176164650 | TAGCCAGCCAAAAGA[C/T]CAAGGTATATGCTGG | 64326 |
rs183185529 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176127347 | CTGACCAACTTCTCC[A/C]CTCTCCCCATCCACC | 64326 |
rs183189228 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176108701 | TTATTCTATATTTTG[C/T]TTTTATTTATTTGCA | 64326 |
rs183195297 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176181983 | TAAGAAAGCAATGGG[A/G]CTTTCCAACAATGAC | 64326 |
rs183197800 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176044691 | TACTTATTAGCTGTG[A/G]CTCTGGCTAATTTAG | 64326 |
rs183207117 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176139906 | TTTAGCATCACACCA[C/T]ATATCTACGTAAGAA | 64326 |
rs183211380 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176197968 | GGTGAAAAACCTCAA[A/C]TGAAAAGCATAAACA | 64326 |
rs183217874 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:176077682 | GTAAGAAATAAATGG[C/T]ATCCAAATAGGAAAA | 64326 |
rs183255674 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176098736 | GGCAAAATAAATAAC[C/T]TACCTGGAATAATTT | 64326 |
rs183258111 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176203947 | CCACCCCAGCCTCCA[A/G]TTCAGGTACGTCTTC | 64326 |
rs183272392 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175954918 | ATTAAAATTGGTTTT[A/C]AACATTAAAAAATAT | 64326 |
rs183291513 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176188907 | TATGTGAAATGTTCT[A/C]ACATACATGTAATTG | 64326 |
rs183292050 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176130265 | AATACTCTAGAAGGG[C/T]AGATAGGATGTATAT | 64326 |
rs183295065 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176128071 | TTACTCATTTTAAAA[A/C]TAGGGGTGTTTCATT | 64326 |
rs183302665 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176164888 | TAGGAAGGCACTTTA[C/T]AGACAATATCTTACA | 64326 |
rs183314764 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176168647 | GTGGTAATGGAGGGT[C/T]GGACTTCCAGCCCTT | 64326 |
rs183322481 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | RFWD2 | GRCh38.p7 | 1:176203269 | GTGAACCCGGGAGGC[A/G]GAGCTTGCAGTGAGC | 64326 |
rs183379246 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175998560 | ATTATCTTCTGTGAA[C/T]GGAAATATATTTAAA | 64326 |
rs183386290 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176000317 | CATTCTTCTGCAAAC[A/G]GATATCCAGTTTTCC | 64326 |
rs183397962 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176014255 | GACTTCTGCTCCTGG[A/T]CCCCACCCAACCAAT | 64326 |
rs183402949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176027433 | TAATGATGGCATACT[A/G]TATACTTCTAATTTA | 64326 |
rs183404567 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175960275 | TCAAAGCTCTAACGC[C/T]TCTAGACTTTTCATT | 64326 |
rs183416090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175965178 | CTTCTCTCCTCATGT[A/G]GGAGGTCATGGACTC | 64326 |
rs183420028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176073371 | ACATAAGTAAAAATA[C/T]TGAAAAACTCTCTAG | 64326 |
rs183423020 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176050707 | ATCAATACTACTTGA[A/C]ACTTCCATAACATAC | 64326 |
rs183432263 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176033233 | CCTGACCAACATGGT[A/G]AAATCCCATCTCTAT | 64326 |
rs183438639 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176108974 | AAAATTAGCTGGGCG[C/T]GGTGGTGCGCACCTG | 64326 |
rs183439383 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:176095579 | CCCAGCTATTGGGGA[C/G]GCTGAGGTAAGAGGA | 64326 |
rs183443055 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176124988 | GATGATATTTCATTG[C/T]AGTTGTGATTTGCAT | 64326 |
rs183444659 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176089572 | AAGTAAAAAGTACTA[A/C]GGTACTGTAATGTAT | 64326 |
rs183500881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176081469 | TAATAAAAAATGTCT[C/T]GGTTCTTTGAAAGAT | 64326 |
rs183515773 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175975478 | GCAGTGCCACGATCT[C/T]GGCTCACTGCAATCT | 64326 |
rs183518319 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:176054883 | AAAAGTTTTCCATAA[A/C]CTCTCCTCTCGTTCT | 64326 |
rs183527482 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:175991670 | ATTGTACAGCTGGAC[A/G]AAAGTATTTCCTTTT | 64326 |
rs183533540 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:176019549 | ACCACCAAATCATAA[C/T]AAAAAAAAAAATCAA | 64326 |
rs183536809 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | RFWD2 | GRCh38.p7 | 1:176150089 | GGTTCCAGGAATTTT[C/T]GTTAAACAAGTGCCC | 64326 |
rs183569040 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176185415 | TGGTACTTTAAATAC[C/G]AATTGTAATCCTCTT | 64326 |
rs183660817 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176077890 | GAAATAAAAAACACA[A/C]TCTTATTTACAATAG | 64326 |
rs183660937 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176096231 | CAAAACCTCTCACTT[C/T]CGCTTCTGAGCCTTT | 64326 |
rs183667434 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176030948 | GGAGAGAGAGATTTA[A/G]AGACAAAGGCACAGT | 64326 |
rs183673172 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176057123 | TTTCCAATATTTGCT[A/G]AACATTCCAAACTTA | 64326 |
rs183675270 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176128421 | TCACAATCAAGATTC[C/T]TTAAGATTCTTCAAT | 64326 |
rs183675879 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175986403 | AACTCCACTTTATAA[A/G]ACCCAGTAGCATAAC | 64326 |
rs183683000 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176147824 | AAGGAATTCTCCATT[A/C]TCTCTCCAGAAATGC | 64326 |
rs183691641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176115235 | GGGTAGATCACCTGA[A/G]ATCAGGAGTTTGAGA | 64326 |
rs183739355 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176175526 | CACAATCAGGTTCAT[A/C]CTCCTCTGAGAATCT | 64326 |
rs183747010 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176209011 | TTGAACCCAGAAAGC[A/G]GAGGTTGGAGTGAGC | 64326 |
rs183748838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176191882 | TATGAATAAGGAGAC[A/G]AGAGGTAAGGAAGAA | 64326 |
rs183761719 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176037601 | AGAAATACAGAAAAA[G/T]AATAATACATTCATG | 64326 |
rs183764826 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176004816 | GTCTAAAATTCTCTT[G/T]TTTGGTTGTGTCTCT | 64326 |
rs183778825 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176094724 | AGTTAATAGGCATAC[C/T]ATGAAGATAAAAGAG | 64326 |
rs183807238 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176186690 | AACCAGATCATTCTA[C/T]CTGCTATGCTGAAAA | 64326 |
rs183816819 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176156441 | ACTCAAACCGAACTA[C/T]ATCAATAATTATATT | 64326 |
rs183842372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175968998 | GATTGCTGATTAATA[C/T]TGAGAAGAGCTCCTC | 64326 |
rs183844132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176190775 | TATCTTAGAACTGTC[C/T]AACAAACTAATATGT | 64326 |
rs183855364 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175988958 | CTACTACTATACTGC[A/C]AGTAGATAAAATACA | 64326 |
rs183860669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176000993 | CTTTGAAACATTATG[A/G]CCATACATATTACAT | 64326 |
rs183882696 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | RFWD2 | GRCh38.p7 | 1:175944578 | ACAACATGGTACTTG[C/T]TGATGATATAAATCT | 64326 |
rs183891546 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176178738 | GGCACCTGTAATTCC[A/G]GCTACTCGGGAGGCT | 64326 |
rs183907242 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176141310 | GTTCAAGACCAGTTT[A/G]GCCAATAAGGTGACA | 64326 |
rs183945678 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176102107 | ACCCATCTGCACACT[C/G]AGAGGATGGGGTGGG | 64326 |
rs183950317 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176119618 | ACCCATTAATTCTGC[C/T]TAATATATACATTAT | 64326 |
rs183953410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176084344 | GTTACTTTTTCCAAC[A/G]AAATAAGAGGACACA | 64326 |
rs183971089 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176153752 | CCCTTATTATTTTGC[A/G]GTATGTTCCTTCAAT | 64326 |
rs183979139 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176171068 | AGGTGGAGCTTGCAG[A/G]GAGCCGAGATCACAC | 64326 |
rs183983644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176194414 | GGAGGCCGAGGCAGG[C/T]GGATCACAAAGTCAG | 64326 |
rs183983667 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176134247 | AGATTCCATTAAATC[A/G]TTATCCTAAACAGAG | 64326 |
rs183988423 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176105957 | TCTAACCTCCAAGCT[A/G]TCCTTGTTCATTACT | 64326 |
rs183997435 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | RFWD2 | GRCh38.p7 | 1:176006622 | AAGCTTAGTTTGGCT[G/T]GATATGAAATTCTGG | 64326 |
rs183998972 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RFWD2 | GRCh38.p7 | 1:175987488 | GAATCTTAAATTACA[C/T]TTAGGAAGATTTCCA | 64326 |
rs184004481 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176087095 | CTTCCTTATACCTTA[C/T]ACAAAAATTAATTTA | 64326 |
rs184017786 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | RFWD2 | GRCh38.p7 | 1:176173938 | GCTGCAGTGAGCCGA[A/G]ATCGTGCCACTGCAC | 64326 |
rs184018268 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176157608 | AAAAACTGCTCTGCT[C/T]CTCCCTATCATACCT | 64326 |
rs184024555 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176123293 | ATGGGACTTCGGTAG[C/G]AGAGATGTCATGAAC | 64326 |
rs184031002 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176136999 | GCAATCTGCCCGCCT[A/C]AGCCTCCCAAAGTGC | 64326 |
rs184032253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176190940 | AATAATAATATTACT[A/G]AGATAATCAGAGCCA | 64326 |
rs184038385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176041146 | ATACAATGCAGCACA[C/T]AGAGATTTCTAAATA | 64326 |
rs184043068 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176174722 | CACCAAAGTACTAGC[A/T]GGTCAGAATCTAATA | 64326 |
rs184044523 | snp | C/T | | | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176208311 | AAAAAGTACAAAAAA[C/T]TAGCTGGGCATGGTG | 64326 |
rs184055609 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:176159466 | TGTCAATATCAAATA[C/T]TTAATAAGATTAAAA | 64326 |
rs184060869 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176117277 | GGTAAAATAACAATA[A/G]TCTTGTCTTTGTAAC | 64326 |
rs184066576 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176080812 | CTGGCAAATTCTACA[A/C]AATATTTAAGGAAGA | 64326 |
rs184080386 | snp | A/T | 0.0217592 | 0.102011 | intron-variant | RFWD2 | GRCh38.p7 | 1:176035265 | AAACTATTTTTTTTT[A/T]AAAAAGAATCAAATG | 64326 |
rs184082279 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176193786 | AAGTAAATTAGTGAT[C/T]GTAAGGGAAGAGGAA | 64326 |
rs184087670 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176016334 | AGAGGTGAAAAAAAA[A/C]CAGAGGGTGTTGTTT | 64326 |
rs184139357 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175973712 | TTCTACAATGGAAAA[A/G]AGTAAGTCTAGATCA | 64326 |
rs184147074 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | RFWD2 | GRCh38.p7 | 1:176005658 | TCCATGAAGTTGAGC[A/G]GTTTTGAGTGAGATT | 64326 |
rs184173180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175994506 | AGGAAACCCGTCTCA[C/T]GTGCAGAGACACACA | 64326 |
rs184179067 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | RFWD2 | GRCh38.p7 | 1:176060256 | TGATAGACTATATTC[C/T]GAAAAACTTTTGTGA | 64326 |
rs184186396 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175993339 | AAAAGCAGAGTGCCT[A/C]TCCTCCTCCAAAGGA | 64326 |
rs184190816 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176023130 | CTGAGAAATAACAGC[A/T]CTCCTGGCCTATCTG | 64326 |
rs184193942 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176106512 | TAAACTGCTCTTAAG[A/T]TCAGTGCTTGAGATA | 64326 |
rs184195003 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175966977 | ATTGGGATTTCTTCA[A/T]CACAAAGGAACACTT | 64326 |
rs184196066 | snp | A/C/G | 0.00279258 | 0.0372817 | intron-variant | RFWD2 | GRCh38.p7 | 1:176008025 | GGACCCTCGGAGCCA[A/C/G]GTGCGGGATATAATC | 64326 |
rs184199624 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:176098259 | TTAAAACAATTTACC[A/G]GGTTTTAAAGGTAAA | 64326 |
rs184208396 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175978679 | CAAAAGCTCATTCAG[A/G]TTGGCCCTCTTCCAG | 64326 |
rs184214006 | snp | A/T | 0.0588605 | 0.161139 | intron-variant | RFWD2 | GRCh38.p7 | 1:176070364 | TTAACTTTTTTTTTT[A/T]AATTAAAAACTCTGC | 64326 |
rs184216408 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176064047 | CATCCTTAGAGCCTA[A/T]ACAAATCTTTTTTAA | 64326 |
rs184220257 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176042654 | GAGAATTGCTTGAAC[A/G]CAGGAGGTGGAGGTT | 64326 |
rs184224997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176090157 | TTGAACCAAGAGTCA[A/G]TCTAAAAATCTCTGA | 64326 |
rs184227914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176024751 | TGTTAGAGATACAAG[A/G]GAGATATATAAAAAT | 64326 |
rs184245573 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176083259 | GTTATCCTATTCATT[C/T]CCATTTTGATATCAA | 64326 |
rs184245864 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176101177 | CAACATCAGTGAAAG[C/T]TGCTTTGACACCCAT | 64326 |
rs184273124 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175973262 | GTAAAAGAGTTAACT[C/T]TGCAAATGGAAATAC | 64326 |
rs184273960 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175951033 | GGCGGATCACCTGAG[A/C/G]TCGGGAGTTTGAGAC | 64326 |
rs184279838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175991806 | ATAATCAATATCACT[A/G]TTTTCACCTCCACGT | 64326 |
rs184282751 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176021269 | ATTGGTTTTTAGAAA[A/T]ATAAAATCCAGCATG | 64326 |
rs184289797 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175991968 | AAGTGTAAGAAGTAC[A/G]GTCTATAATAATGGT | 64326 |
rs184293056 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176048520 | GCACCATAACTATAA[C/T]GATGACAACTATTCA | 64326 |
rs184300851 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:175949655 | GACTCTGGTCTGCAA[C/G]AAAGCTACTGCCAAG | 64326 |
rs184313352 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176038364 | CAATCAAAATCTCAG[C/G]AGGATTTTATGTAGG | 64326 |
rs184320024 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176019691 | CATAGTGAAAATACG[G/T]TTTTCCAAAAAATAT | 64326 |
rs184331907 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176087529 | TCATTGGCCATCAGA[A/G]AAATGCAAATCAAAA | 64326 |
rs184387784 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:175996191 | GGCCTTTGACAAAAT[G/T]CAACAACCCTTTGTG | 64326 |
rs184390902 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | RFWD2 | GRCh38.p7 | 1:175952201 | CCATGGCAGGCGGAT[C/T]GCCTGAGGTCAGGAG | 64326 |
rs184395023 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:175973821 | TATAATGGCATTATC[A/G]TATGTAACAAACAGA | 64326 |
rs184407313 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176010930 | AAATTGTCTATATTA[A/C]CATTTCCTCAGTGGT | 64326 |
rs184423830 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175956732 | AATAAGATTATTGTA[C/G]TATACTTCTTAATCA | 64326 |
rs184448610 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176137483 | TAACGCCAGGATGCG[A/G]TTGTCTTACTCTAAC | 64326 |
rs184452788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176165219 | TTACAAAGTATACAC[A/G]CAGAGATCAATCAAA | 64326 |
rs184485702 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176199164 | CTACTAAAAATACAA[A/C]AAATTAGCTTGGCAT | 64326 |
rs184568731 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175976901 | TCTTAGCAATTAAAA[G/T]AAAAAATGATAAACT | 64326 |
rs184590674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176157714 | TAAAGGATTACAAAA[A/G]TATTCAGCACTGAAC | 64326 |
rs184595310 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176123856 | CATGTCAGTAACACA[C/G]ACTTATCACCAATTA | 64326 |
rs184600237 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176183949 | GGAAGGGGAAATGGG[G/T]AATTGTTGTTTAATG | 64326 |
rs184610559 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176067868 | TACCCCCAGACACTG[C/T]TGTGGGGTCAGAGCC | 64326 |
rs184626094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176046575 | TGTTCCAAGACACCT[A/G]ACATGCTTTTCATTC | 64326 |
rs184632255 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176029362 | TGACTAAGCAAAATA[C/G]GTCTGATTTGAAAGC | 64326 |
rs184634880 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992413 | GAGAGTGGGTGCAGC[A/G]CACCGTGCGCGAGCC | 64326 |
rs184638934 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:176105388 | CAAATCCAAATAACC[C/T]TTGAATATACTATAT | 64326 |
rs184649081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176086746 | ACTTTCTTCACAGAA[C/T]TGGCAAAACTACTTT | 64326 |
rs184652473 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176052139 | AAGTGCCCTATACAC[A/G]TGTACCAGTTTCTAT | 64326 |
rs184675215 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176090925 | GTGAGATAATTAAAA[A/T]GAAACCCACAGTTAG | 64326 |
rs184691220 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176195257 | ATATTATCAGGAATA[A/G]AGAGTGACATTTCAA | 64326 |
rs184705709 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176205340 | AGATTAATTCTGATA[A/C]AGAATAACGTACAAA | 64326 |
rs184721923 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176125864 | TCATTAACATGGCAT[A/G]CCTTTCCAGTTTTTT | 64326 |
rs184733248 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176199210 | TAATCCTAGCTACTC[A/C/G]GGAGGTTAAGGCAGG | 64326 |
rs184735437 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176200242 | TATTTGAGCACTTAT[C/T]ATTATGAGTATTTGT | 64326 |
rs184750053 | snp | A/G | 0.000597193 | 0.0172696 | intron-variant | RFWD2 | GRCh38.p7 | 1:176160303 | TAAGTTCTGGGACAC[A/G]AGTGCAGAATGTGTA | 64326 |
rs184797747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175957043 | AATGTGTTTGTGTTT[C/T]AAGCTAAAAGTTATT | 64326 |
rs184808391 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RFWD2 | GRCh38.p7 | 1:175978182 | CTTAAAAATTGGCAT[C/T]AATTCTATGCTTCAA | 64326 |
rs184820127 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176110089 | AGACTGCCTGTCTGT[C/G]TCTATCTGTTTATTT | 64326 |
rs184823855 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176074337 | AATATAAGAAAGTAA[C/G]AAAAGCAAAAAATCA | 64326 |
rs184838358 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176208679 | TACATAATTGTTTTT[A/C]AACCGTTATCCTTGG | 64326 |
rs184843084 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | RFWD2 | GRCh38.p7 | 1:176142670 | TATATTCAAAGAAAG[A/G]AAACACAACTTTCTG | 64326 |
rs184846611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176148881 | AAATCTTAAGGAAAC[C/T]TCCTAAAAATTCAAA | 64326 |
rs184857358 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175994061 | TGGGCAGAAACTCTA[A/C]AAGCCAGAAGAGAGT | 64326 |
rs184861702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176184393 | TTAACAATTAATAAA[C/T]GCAGAAGTTTTCAAA | 64326 |
rs184872716 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176128785 | TCCTGCATTAAAAAA[A/G]ATTTCCAAATAAAAT | 64326 |
rs184907482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176184186 | TAACCTGGCATGATA[C/T]AATGTAAAGTTAATA | 64326 |
rs184913245 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176166126 | GCCTGTATTTATTTA[A/T]TTTATTTATTTATTT | 64326 |
rs184925262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176091581 | GTGAAAAAAGTTGCA[C/T]TCTGGAGCTCTTGTA | 64326 |
rs184926085 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176011205 | GTACAGTAGTCACTA[C/G]CCACATGTGGTTATT | 64326 |
rs184931506 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176075118 | TATATGCCTAGTCTG[G/T]CCTAGCCTGCACTAC | 64326 |
rs184937730 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176053408 | TGCTCCTCTACCAAC[C/G]CACGAGTTCTTGGAA | 64326 |
rs184941678 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176126301 | TGTTGAGTTCCAGAT[C/T]TAAGAGGAAAGGTTT | 64326 |
rs184949327 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | RFWD2 | GRCh38.p7 | 1:176144018 | ACCTAATGGTGACAC[A/G]TTGAATGCTTTCACT | 64326 |
rs184951423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176111101 | AGGTTGCAGTAAGCT[A/G]AGATGGCGCCACTGC | 64326 |
rs184953129 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176166571 | CTACATTTACCAAAC[A/G]AAGTTTTTTACTACT | 64326 |
rs184953536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176186058 | TAAATACATAATAAT[A/G]AGAGGACACACCAGC | 64326 |
rs184953974 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175983800 | TGCTGGGAAATAGAG[C/T]AAAGAAGACTCTTGT | 64326 |
rs184957686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176151161 | CAAAACTTCCAAAAA[A/G]CATGTAATGATCATT | 64326 |
rs184958759 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176060238 | ACAAATAAATACACT[A/G]CCTGATAGACTATAT | 64326 |
rs184959361 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176169740 | TGGTAGTCACTGAAG[G/T]CTAGGCTGGCTGTGG | 64326 |
rs184962133 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | RFWD2 | GRCh38.p7 | 1:176047103 | AAACACAGTTGTTAC[A/T]TAACCAGCTGGAAAT | 64326 |
rs184963951 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176200447 | TAAAGACAGAGGATT[C/T]CAATGCACTAGACAC | 64326 |
rs184965072 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176204089 | CTAAATACATGTACT[C/T]GAACTTACAGATCTG | 64326 |
rs185003711 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:175962628 | TGAATATCAAATAAA[C/T]TTGTATGCCTTTTCT | 64326 |
rs185010829 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176034416 | CTCTGTGTATATAAA[A/G]AGGAGCATCTGTGAT | 64326 |
rs185015071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176000738 | ATGTTGCTTTTTTTT[C/T]TGTTATGTCATTTGC | 64326 |
rs185045327 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176073704 | TATTGTTTAATAGTC[G/T]AGATACTGTCAAAGT | 64326 |
rs185063602 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176069162 | TGCACTCCAGCCTGA[C/G]CAACAGGGTGAGACC | 64326 |
rs185075562 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176029632 | GTACTGTTGTTTTTT[A/C]AAAAAGCTCTCCAGG | 64326 |
rs185092835 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176035446 | ATAATTAAAATCCCA[G/T]AGGAGAGGAAAAAGA | 64326 |
rs185113728 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175988666 | AGCAAAACACCGTCT[C/T]TACTAAAAATACAAA | 64326 |
rs185117498 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176051582 | TCTTCTACTTATTTT[A/T]AAAAAAAACAAACAA | 64326 |
rs185120397 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175964247 | TACCCCAAGACAGAA[A/G]GTAATAAATGACACA | 64326 |
rs185124603 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:175984367 | AGCTTCCATGTGGTG[C/T]TGAGCCTGCGTGTGC | 64326 |
rs185125693 | snp | A/C/T | 0.00239393 | 0.0345281 | intron-variant | RFWD2 | GRCh38.p7 | 1:175957744 | TATGAATGTTTACAG[A/C/T]GGCTTTATTAAAAAT | 64326 |
rs185131909 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176015900 | AAAAGGAGCCAGAAA[A/G]AGGAAAATTCTTCTG | 64326 |
rs185133537 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175997641 | CAGCCAAAAAACACA[C/T]GAAAAAATGCTCATC | 64326 |
rs185141091 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175967898 | TTTGAGATGGAGTCT[C/T]GCACCGTCACCTAGC | 64326 |
rs185167619 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176119410 | GATATCTCAGTGTAT[A/C]CAGTGATATAATTCT | 64326 |
rs185177506 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | RFWD2 | GRCh38.p7 | 1:176097573 | TTTTTTTTATAGAGC[C/T]TTTTTTATAGACTGG | 64326 |
rs185184626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176011576 | TTAACAATCAAATCA[A/G]TCTTTCTAGACAATG | 64326 |
rs185185380 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:176116875 | AAGCAATTTACCACT[C/T]CAACCCACCACCTCA | 64326 |
rs185192413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176080339 | AGGTATCAACTAAAG[A/G]ACCTCAATTTTTATC | 64326 |
rs185195285 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176149556 | ACCTACTTATTCACA[A/G]ATGTGAGAATATATT | 64326 |
rs185210125 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176167443 | GAATGAATGAATGAA[A/T]GAAATCTTGATGACA | 64326 |
rs185212051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176129741 | ACTCACCATTCCAAA[A/G]TTCCTTAAAGACAAA | 64326 |
rs185258391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175961935 | ATGGTTTTGGAATGA[C/T]GACAAATTGTGTGGA | 64326 |
rs185283418 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176133200 | TACGTACGTATATGT[A/G]CGTATGTACACACAT | 64326 |
rs185287510 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176170491 | TATCAGAGCTCTTGG[A/G]TGACCAGGTGCATTG | 64326 |
rs185313950 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176204593 | TATTAAACCTCACCA[C/G]AAAAAGAAATAATTA | 64326 |
rs185336695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175982244 | ACACTCTTTTATTCA[C/T]TGCATTATTCACAAC | 64326 |
rs185368578 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175991127 | TAAGTACAATAATAC[A/T]TACTTAACAATGGAG | 64326 |
rs185379199 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176002422 | AGGTTAGTTACATAT[A/G]TATACATGTGCCATG | 64326 |
rs185396062 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176018563 | AGCCATCTTTTCCTA[C/T]TCTCAATCCTTGAGG | 64326 |
rs185396239 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176064864 | CCTGGGCTCAAGCAA[C/T]CTGCCTGCCTCAGCC | 64326 |
rs185400041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175947117 | CTCTAAGGCTCAGTA[C/T]AATGGTGTATTTCTA | 64326 |
rs185408552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176153154 | CAATTCTAGCCTCTT[C/T]CATCAAATTTTCTAT | 64326 |
rs185415841 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175971814 | CTTTTGCTACTGAGG[A/G]GACTGATGAGAACCC | 64326 |
rs185420392 | snp | C/T | 0.021333 | 0.101051 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176186342 | GAGACCTCATCTCTA[C/T]AAAAAAAAAATTAAA | 64326 |
rs185424616 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176076334 | TCTCTCAAAACTACA[C/T]AAAAACATTAAAATT | 64326 |
rs185429002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176054309 | TGGGATTACAGGCGT[A/G]CACCACCATGCCCAG | 64326 |
rs185441155 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176036891 | CCATTGTAAGTGGAG[A/G]AGCATTTTATGGACT | 64326 |
rs185463247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176021539 | AATGACTAATAAATA[C/T]GGGACATAATTTTTT | 64326 |
rs185475312 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176079789 | AACCACTGCTGAATG[A/T]GGGTGATGGTTATGT | 64326 |
rs185477542 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176059814 | CGTCAGTGGTTCCAA[A/C]AAAACTTCATTTATG | 64326 |
rs185485684 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176039798 | GACAAGGGTGCCAGA[A/C]CATTCAATAGGGAAA | 64326 |
rs185492154 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176193679 | TGAGCCTTAGAAACA[C/T]GTTAAGTGAAAGACA | 64326 |
rs185494686 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176122775 | AAAGCAAAAGAGCAG[C/T]TCATTTGAAAGTTTT | 64326 |
rs185501788 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176058804 | CAGATCCCATATATG[A/C]ACCTGAAACTTCTCC | 64326 |
rs185522391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176096860 | CTCCATCTTGTTTTA[C/T]GTCCTTCAGAGCCAG | 64326 |
rs185545086 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176189291 | GCATTTATTTCTTTC[A/C]GTCCATTTTGAAACA | 64326 |
rs185553407 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176172787 | CAGGAACACATGGAT[C/T]GACATATCTCAATGA | 64326 |
rs185559485 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207887 | GTCAGTGAAGTTTTC[A/T]GCGAATTGCAAACAT | 64326 |
rs185560573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176118642 | ACGCCTGGGGTTCCA[A/G]CTACTCAGGAGGGTG | 64326 |
rs185602946 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176006018 | CAGGACTTGCTTTAT[G/T]AGTCTGGGTGCCCTT | 64326 |
rs185612464 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176079156 | ACGCACAAAAGAAAG[A/T]AAGTTGTTCTTCCAT | 64326 |
rs185624637 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176180341 | CAGTATTTCTTACCC[C/T]AGTAACTCTAATTCA | 64326 |
rs185625412 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992512 | GAAAGGAGTGACAGA[C/T]GGCACCTGGAAAATT | 64326 |
rs185627669 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | RFWD2 | GRCh38.p7 | 1:175965651 | TGGACTGCAGTGGTG[A/C]AGTCTCGGCTCACTG | 64326 |
rs185636683 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176039233 | AAAAAAGGAATCTCA[A/G]GGGAAATTTAAAATA | 64326 |
rs185646183 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176022069 | TGTATTTTGAGGCAA[C/T]GTTATTACATACACA | 64326 |
rs185653089 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176136608 | GCCAAACCAAAATGG[A/C]ATCACCATGATCATA | 64326 |
rs185654862 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176006301 | TCTTGACTCTTTATC[A/C]AATTTGCCAGTCTGT | 64326 |
rs185659194 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176115597 | ACTAAAACTACAAAA[A/G]AATTAGCTGGGCGTG | 64326 |
rs185664671 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175974094 | AACACTAACAGATTT[G/T]AAACAGTGAGATAAA | 64326 |
rs185671069 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175945906 | GCTTTTGTCTTTATA[G/T]TAGGTAACTAGGCTA | 64326 |
rs185683618 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175970202 | GTAGACTGCATTCTA[C/T]AGGTTCATCAATAGC | 64326 |
rs185699869 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:176131754 | GTCTGATTTCAAATC[A/G]TAATCTTAAGGATCA | 64326 |
rs185700014 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | RFWD2 | GRCh38.p7 | 1:176100876 | CCCCACCCCCCAAGA[C/G]ACATTTTTGTCTCAA | 64326 |
rs185716177 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176007887 | CCAGTTCCAGCTTCC[C/T]GGCTGCTTTGTTTAC | 64326 |
rs185730956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176082315 | TTTTTCAAGGTAAAT[A/G]TTCATGATTTCCCTT | 64326 |
rs185745051 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175989200 | ACAGACCAGAAACCA[A/C]ACTACTTTAATTGGA | 64326 |
rs185750369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176194663 | ACAACAAAGGCAGAT[C/T]GTCATACTAAATAAA | 64326 |
rs185753527 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:176042542 | CACTCCAGCCTGGGC[A/T]GCAGAGCGAGAATCC | 64326 |
rs185754487 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176161123 | CATTCAGTTTCCTCA[C/G]ATCTACTTATCTGTT | 64326 |
rs185756771 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176124609 | ACAGAATCTTATTCA[C/T]TTTATGGCTGATAGT | 64326 |
rs185760815 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176139414 | GGGAGATTTCTCAAA[C/G]AGCTTATTAAAAGAG | 64326 |
rs185772121 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176108669 | TAACTATCAGATGAT[G/T]TCTTTGGTATCTAGT | 64326 |
rs185794088 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | RFWD2 | GRCh38.p7 | 1:176158565 | ACATTTAGAAGTAAA[A/C]TATATGACATAAAAT | 64326 |
rs185794254 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176177031 | GGTGTTTAATACAAG[A/G]TTATCTGTAAATAGC | 64326 |
rs185810046 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176006488 | GCAGTGGCTGGTATG[A/G]GTTGTTCCTTTTCAT | 64326 |
rs185831580 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175975153 | GTTGATGCAAATCTC[A/T]GTATCTAAAATACAT | 64326 |
rs185838110 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176001393 | AGTATAGTAATTCTC[A/T]GTCAAATTTTCTCGA | 64326 |
rs185842640 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176024372 | CATATTACTATAGTA[C/T]GGGACATCAACCTCA | 64326 |
rs185843887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176040804 | AAGGCATAACATGAT[A/G]CGAAATAAAGCTTCC | 64326 |
rs185863913 | snp | A/G/T | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176181702 | AAAAATTAGCCGGGC[A/G/T]TGGTGGCACACGCCT | 64326 |
rs185869739 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176062921 | GTATGGTTCCACTTA[A/T]AAGAAATTTTTAAAT | 64326 |
rs185901263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175953307 | AAAAAAAGAAAGGAA[A/G]TGAGGAACATAGGAA | 64326 |
rs185968975 | snp | C/G | 0.0221141 | 0.102801 | intron-variant | RFWD2 | GRCh38.p7 | 1:175993086 | GGACTTGCGGTTCAC[C/G]AAAAGCCGCTGTTCT | 64326 |
rs185975920 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176044265 | CTGTATTTACATCCC[A/G]AAAGTCTTGACTTGA | 64326 |
rs185982676 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:176022762 | AAATTAGCTCATACC[C/T]AACCTCAATGTGCCC | 64326 |
rs185983978 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176027376 | TCTACGTATTAAAGA[C/T]AAGTGACAGAATAGT | 64326 |
rs185990404 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176009501 | TTATGTCCTTGTGTA[C/G]TGTACAAAAGTTTTA | 64326 |
rs185993844 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:175995234 | CAGAATCTCTGGGAC[A/G]CATTCAAAGCAGTCT | 64326 |
rs186006204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176197550 | GTTGTATTTTGTTAC[A/G]GCAGCCCAAGCAAAC | 64326 |
rs186006521 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176193168 | GGCCAACAAGCTCTT[G/T]AAAAGATGGTTAACC | 64326 |
rs186027652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175959317 | CTTCTTTGTAAGGGT[A/G]TGTATCTACAAAACT | 64326 |
rs186066951 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176149779 | TGTTAAAATTCACAA[A/G]AACCAGGAATTCCAG | 64326 |
rs186088839 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176185089 | ACTCTTTTCTTCCTA[A/T]CCCAAATAAAGCTAA | 64326 |
rs186095108 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176168293 | AGAACTCCTGACCTC[A/G]TGATCCGCCCGTGTC | 64326 |
rs186099343 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176203051 | GATTAAAAGTCAACC[G/T]TCTCGGCCGGGCGCG | 64326 |
rs186119347 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176177780 | TTAACAAAATACAAA[A/G]TAAAACAAACAAAAA | 64326 |
rs186121211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176140131 | ATTAAACTCTAATGT[C/T]TTCTCTGAAAATAAT | 64326 |
rs186121421 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176202309 | ATCCTCCCATCTCAG[C/G]TTCTTGAGTAGCTGG | 64326 |
rs186174780 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176163580 | TTCAAATGTCAAGTA[C/T]TCAAAGACAAATGTT | 64326 |
rs186183331 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | RFWD2 | GRCh38.p7 | 1:176196344 | AAAGACTAAAAAAAA[A/T]TAATAATCCTCTAGC | 64326 |
rs186197264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176104162 | GATGAAATTAAATCC[A/G]CATTTCAAAACATAC | 64326 |
rs186199345 | snp | A/C | 0.0118329 | 0.0760029 | intron-variant | RFWD2 | GRCh38.p7 | 1:176085912 | TAATAAGAAAAGACA[A/C]AAAACTTAGAATAAA | 64326 |
rs186216843 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176162767 | CTGAGTAAAAATGAA[A/T]GGATTAGTGAAGCTA | 64326 |
rs186217597 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:176124783 | TCTTTTGGATATATA[C/T]CCAGCAGTGGGATTG | 64326 |
rs186231383 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176144825 | AGCTAGATATCCATA[A/T]GAAAATATCTCTATA | 64326 |
rs186233490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176180830 | AGGTGTAAAGAAAGA[C/T]CAAAAGTATGGTGCA | 64326 |
rs186234292 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176159250 | GGAAAATGGACACAA[A/T]ATATGAATAGGTAAT | 64326 |
rs186238319 | snp | A/T | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176184831 | CATTCTATCAATAAG[A/T]GATGAAATTTCTATT | 64326 |
rs186239690 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176121713 | TTAAAATGAAATCTT[A/C]TCTCATTGCCTGTTT | 64326 |
rs186290963 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176054610 | TCTTGTCATTCCGAA[C/T]GATGTGCTCCTAGAT | 64326 |
rs186293410 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:175994896 | TGCACCAAGCAGACT[C/T]AATGGACATCTACAG | 64326 |
rs186304649 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176025543 | TATATAGGAAAAAAA[A/T]TTGACCAGAAAAGTC | 64326 |
rs186311941 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176181560 | CTTAAAACACATTCT[C/T]GGCTGGGCGCAGTGG | 64326 |
rs186321353 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176145252 | TGTAGTACTAGGTGC[C/T]CAACCTCATAAGTCA | 64326 |
rs186327069 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | RFWD2 | GRCh38.p7 | 1:176113545 | GGATTTGCTAGAAAT[C/T]TCAAAGTAGTGTTAA | 64326 |
rs186335457 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176126878 | GAAATGCCTACTAAT[C/T]AATCATAATTACTAC | 64326 |
rs186337062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176076840 | GAGATTATTATGAAC[A/G]TCTCTATGCACAGAC | 64326 |
rs186337569 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | RFWD2 | GRCh38.p7 | 1:176092970 | GATTCAACTGAAAAA[C/T]TGTAGTATAGTAACA | 64326 |
rs186339295 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176093976 | TGTAGTAAGCTGAGA[C/T]TGTGCCACTGCACTC | 64326 |
rs186351395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176171646 | GTGGAAAAGTGGCAT[C/T]AAGAGACTTAATGCA | 64326 |
rs186355801 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176127272 | ATTAATTATAACCAC[C/T]TTGTTGCACAACAGA | 64326 |
rs186358865 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176013326 | GAAATTTACTTAGCT[A/G]GGGGGAAAAACACAA | 64326 |
rs186360545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176164545 | AGAGATGTGCTATCT[C/T]TCAGAAAGGAAAGGA | 64326 |
rs186362456 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176205545 | GCCAACTTCCTACAT[A/G]CCTAATATTTGATCA | 64326 |
rs186366393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176188118 | TGGAGGCTGAATTTC[C/T]CAGCCTCCACAAACA | 64326 |
rs186368434 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176145888 | GAAGATGACTGCAAT[A/C]CAAAAAGGGTGGTCA | 64326 |
rs186373872 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:176116057 | CTAAAGTATTTCCTT[C/T]CTCTCAGGTTCTGAA | 64326 |
rs186378532 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176088509 | TCACATGTATGTGTT[C/T]GTCAAATCTCACTCA | 64326 |
rs186380528 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176006709 | TGTAGGGTTTCTGCC[C/G]AGAGATCCGCTGTTA | 64326 |
rs186383996 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176031301 | TCGAAAGATAAAATA[G/T]TATAATCTTTTGGAG | 64326 |
rs186391279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176049295 | TTTTCTACATGTTAT[C/T]ATTTAGTGACATTAG | 64326 |
rs186392276 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176012958 | AGTCCCTAGGTATCC[G/T]CGGGGGAACTGGTTT | 64326 |
rs186399328 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176088128 | GGGATGGGTGAGGGA[C/G/T]AGCACTAGGAGAAAC | 64326 |
rs186414017 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176071357 | GCAAAGCCTGCAGAA[C/T]CGTAAACCAATTAAA | 64326 |
rs186417068 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | RFWD2 | GRCh38.p7 | 1:176048944 | TTGGGAGGCCGAGGC[A/G]GGTGGATCATGAGGT | 64326 |
rs186418045 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176008344 | AGACCGGAGCTGTTC[C/T]TATTCGGCCATCTTT | 64326 |
rs186433912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176108256 | CTGGCTTCACTTATA[C/T]TGTTAGCATTTTTTT | 64326 |
rs186434895 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176124306 | TTAAATGTACAATTA[A/T]ATTATTATTGACTAT | 64326 |
rs186438740 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175979159 | GGAGACCTGGGGAAC[C/T]TTTCAAAATACAGAT | 64326 |
rs186440218 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176043311 | AGATAGAATACAGAT[A/C]TCAAAATGAATAAAG | 64326 |
rs186455662 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176008913 | ACTTAGCAGTAACAA[G/T]ATTTCCTTAATGCTT | 64326 |
rs186516485 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175986606 | ATCAAGCTTATACTG[C/T]ACATAATCAATAAAG | 64326 |
rs186522451 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176112511 | AATGTGTAATAATCA[A/G]TTAGGGTAACTGGTA | 64326 |
rs186523612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175987147 | TAGAATAGAAAAACT[C/T]GGAATTAGGACATCA | 64326 |
rs186529616 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:175953001 | TTCTTGTTTTTAAGT[G/T]TTTTTAAAAGATAAT | 64326 |
rs186536620 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175999844 | GTAGCCATGATTTGC[A/C]TTTCTGATGATCAAT | 64326 |
rs186554002 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176032036 | CTATTTGCACCAAAG[G/T]ATCCTAAGAAAGAAT | 64326 |
rs186557760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176014065 | GTATTTGTATTTTAT[C/T]TTCATGTTTTTGGTG | 64326 |
rs186560292 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175979953 | CATTATGTACAAACA[C/T]GCTGTGTAATGCTAG | 64326 |
rs186562353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175966640 | ATTAAAGCAAAATGG[A/G]AGAAAGAAGAAAGGT | 64326 |
rs186568009 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175995060 | CTCTCAGACCACAGC[A/G]CAATCAAACTAGAAC | 64326 |
rs186588512 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175998875 | CCTGTTAAGCAATAA[C/T]GGAATGGAACTTCAT | 64326 |
rs186592784 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176036045 | AAGAGAAATCAAACA[G/T]AATTTTAAACAGAAT | 64326 |
rs186593247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176072072 | TGAATCATGTATGTT[C/T]TGAATTACCATAGAA | 64326 |
rs186595382 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175959434 | TTATTTAACATTACA[C/T]TAGATGTTCTGGCCA | 64326 |
rs186607836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176097271 | CATTTTTCCTTGCCA[C/T]TCTCAATGCACACAT | 64326 |
rs186621970 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:176129444 | TGCATGACAATTTTT[A/T]AAAAAAAATGAATTA | 64326 |
rs186633077 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176002110 | ATTGAGCTTTTTGGA[A/T]GTGTGGATTGATGTT | 64326 |
rs186634871 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176076051 | TCAATACCCCACTCA[C/T]ACCATTAGACAGATC | 64326 |
rs186639280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175980158 | TAAGGAAATTCAGCA[A/G]GGTCACACAGCTGAT | 64326 |
rs186668859 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176128369 | TTATTGCCATGGAAG[C/T]TTGCTTCCTGTGTTT | 64326 |
rs186723844 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176165865 | AGAAAAGTGATTATA[A/C]TCCAGATAAAGGAGA | 64326 |
rs186725456 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176208047 | GAACCTAGGTTTATT[A/G]TGGATCTGATATAAT | 64326 |
rs186732662 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176190280 | TTTTCTTTGCGTGTC[A/G]TGGTGGCACTCAAAA | 64326 |
rs186732918 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | RFWD2 | GRCh38.p7 | 1:176148292 | AGATAGCCCAGAACA[C/T]AGCACATAACAGACA | 64326 |
rs186740966 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176183982 | TGACGAGTTTCAGTT[C/T]TGCACAAAAAGTTCT | 64326 |
rs186756055 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176049741 | CAGATCATGAACTAA[C/T]TGAAATGAACACTGT | 64326 |
rs186763791 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176032415 | GTATTAGTAGCTAGA[C/T]GTTGTCATACAGCAA | 64326 |
rs186791168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175990019 | TTCTACTCTAACCTT[C/T]ATTATTTCCTTCCTT | 64326 |
rs186804220 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176203951 | CCCAGCCTCCAATTC[A/G]GGTACGTCTTCTTGG | 64326 |
rs186834766 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:176017584 | GGCTAAAGTGCAGTG[A/G]TGTGATCATGGCTCA | 64326 |
rs186848527 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175959919 | AAAGTTTTCTATTTG[C/G]TGGTTATATCCTCCC | 64326 |
rs186857373 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176053718 | AACAATCCTTCAAGG[C/T]CATTGTGATCTAAAA | 64326 |
rs186901347 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:176111832 | GTTAGGTCTAGCTAT[C/T]ATCTGGAGCACAGCT | 64326 |
rs186908679 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176135738 | TGATTAATGAAAAAA[G/T]AGCAAATTTTAAAAT | 64326 |
rs186925792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176081884 | ATTGCTCCTTTTTAT[C/T]TCAAAGTGCCTTCAT | 64326 |
rs186929793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176172269 | CTGGTCGCAAACTCA[C/T]GGCCTCGAATAAGCC | 64326 |
rs186946043 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176131221 | CTGAAAAATTTTAAG[C/G]AGGAAAGAAACATCA | 64326 |
rs186950162 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176100156 | GCACTTTGGGAGGCC[A/G]AGGCAGGTGTATCAC | 64326 |
rs186953747 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176118106 | TTACCCATAGAAGTG[A/C]ATAACCTGACTCTGG | 64326 |
rs186959691 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176169541 | CCAATATACATAAAA[A/G]TTCTGTTTACGCTAT | 64326 |
rs186961348 | snp | C/G | 3.45203e-05 | 0.00415439 | missense, utr-variant-5-prime | RFWD2 | GRCh38.p7 | 1:176206607 | GTCCTCGTAGGAGTT[C/G]ATGAGCCCGTTGCAG | 64326 |
rs186975009 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176151144 | ACATCTCTTACAATC[C/G]TCAAAACTTCCAAAA | 64326 |
rs186976521 | snp | C/T | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176185989 | GCAGACTCAAATATG[C/T]ATAGATGATATTACA | 64326 |
rs186985660 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RFWD2 | GRCh38.p7 | 1:176122118 | GCACTCCAGCTTGGG[C/T]GACAGAGCAAGACTG | 64326 |
rs186991584 | snp | A/C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176136013 | CTTCAAATCATAATA[A/C/T]CCTATAAGACTCCCA | 64326 |
rs186994640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176104413 | TCATAGGTAACAGAC[C/T]AGTATTCCTAATATA | 64326 |
rs186994989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176158206 | AAGACAAAAGATAAG[A/G]ATGACAGCAGACTTT | 64326 |
rs186996186 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176077699 | TCCAAATAGGAAAAG[A/G]TTAAGTCAAATTATC | 64326 |
rs186996903 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176192287 | TTACAGTTAACAGAA[G/T]ATTTAATTCGTCTTG | 64326 |
rs186997760 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176056892 | CAGAAAGAAATAAAG[G/T]ATTCAATGTATCTAC | 64326 |
rs187001829 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176130112 | TCAGAGATAATCAAA[A/C]CTGGTCTAAGTATGT | 64326 |
rs187023114 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | RFWD2 | GRCh38.p7 | 1:176155685 | CCCAAGAAGAATAAA[C/T]ATAAAAATAATAAAA | 64326 |
rs187093567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176092445 | ATTAAAAAGGTGAGA[C/T]AAGATACAAACTGTA | 64326 |
rs187117197 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176005394 | TTTGCCTTCTGCTAG[C/G]TTTTGAATGTGTTTG | 64326 |
rs187130411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175964853 | ACACAAAAAAACTCA[C/T]AATCTATACTATATC | 64326 |
rs187134528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176155014 | CTTAAAAGCATAAGA[C/T]GAATATTTACAAAAA | 64326 |
rs187138487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175973406 | TTTTAAACCAGCCCA[C/T]GAAAATAAAATACAT | 64326 |
rs187140616 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176038458 | TTTTCAAAAACAAGG[A/T]TGAAGGACTTACTAC | 64326 |
rs187144033 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:175997923 | CAAAGGACTATAAAT[A/C]ATGCTGCTATAAAGA | 64326 |
rs187145018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176019766 | CTTGGGAGGCTGAGG[C/T]GGGAGAGTCACTTGA | 64326 |
rs187146418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176188746 | GCAAACCTCACTGTG[C/T]TCTTACTCCTCCACC | 64326 |
rs187147309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176060311 | AAATGTCTTTCTCCT[C/T]AAAGCACTTAAAGAT | 64326 |
rs187156303 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176023131 | TGAGAAATAACAGCT[C/T]TCCTGGCCTATCTGA | 64326 |
rs187161804 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176098283 | AGGTAAAATTGCTAA[A/C/G]AGTTACCATTATAAT | 64326 |
rs187171011 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:175991950 | ATAGTAACTTAAAAA[A/G]ACAAGTGTAAGAAGT | 64326 |
rs187184792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175988943 | AAACCAAAAATAATT[C/T]TACTACTATACTGCA | 64326 |
rs187189582 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176043885 | GATAAAAATAATTTT[A/C]ATGTGTTCAGAAAGA | 64326 |
rs187198584 | snp | A/T | 0.0352966 | 0.128072 | intron-variant | RFWD2 | GRCh38.p7 | 1:176041814 | CTACTAAAAATTTTT[A/T]AAAAATTAACTGGGT | 64326 |
rs187204184 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176117531 | CAACAACTGAAAATC[A/G]CATGACATACATACC | 64326 |
rs187205845 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176023588 | CTGGGAGTGGTGGCA[C/T]ATGCCTGTAATCCCA | 64326 |
rs187209551 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | RFWD2 | GRCh38.p7 | 1:175993542 | ACCAATACAGAGAAG[G/T]GCTTAAAGGAGCTGA | 64326 |
rs187211197 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176007417 | TGGAGGAAGAGAGGC[A/G]CTCTGGTTTTTAGAG | 64326 |
rs187219124 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176084774 | ATCTAAGCAATATGT[A/G]GATTATAAATAATAT | 64326 |
rs187228173 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176081713 | TTGTTTAAAATCCCG[C/T]TTATAATAACATTTT | 64326 |
rs187230395 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176098844 | CAAAATTGTCTTTCC[A/T]GATGCCTAGCTTTTG | 64326 |
rs187237243 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176154194 | TTGTATATCTGGCAG[A/G]GCTACTTATTACTGA | 64326 |
rs187239994 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176061574 | GAGGTTGCAGTCAGC[C/T]GTGATCACGCCATTG | 64326 |
rs187270243 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176121403 | ACAAGTAGTCAAATA[C/T]ATCACCCAAAATCTA | 64326 |
rs187285459 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176141833 | CCTCCTAGGCTCAAG[A/C]AATTCTCTCACCTCA | 64326 |
rs187292973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176160006 | ATTCAGGTTAAATAA[C/T]AATGAAAAGTAAAAC | 64326 |
rs187297658 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176125635 | ACTATAGCTATATAG[A/T]ATAATGTAAAATCAG | 64326 |
rs187308628 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176179058 | ACTTTGGGAGGCCAC[A/G]GTGGGTGGATCACTT | 64326 |
rs187322715 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176194304 | AAACCAAGCACATCA[C/T]AATTATGTTAAAATG | 64326 |
rs187331975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175985192 | TTCATCTTGTAAGCA[C/T]AGCTACTTTCAAGCT | 64326 |
rs187343146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176041547 | AGAGACAGGGTTTCA[C/T]CACATTGGCCAGGCT | 64326 |
rs187372295 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176138485 | CTGCCGCCTTAAAAT[A/G]TGTCACACAATGCCA | 64326 |
rs187376893 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176080950 | TACAACCTTATGAGA[A/T]GGATACTATCAATTA | 64326 |
rs187396679 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175972993 | ATGCGCCACCACACC[C/T]GGGTAATTTTGTATT | 64326 |
rs187399481 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175945389 | CTATCTCCACAGTTA[A/G]CTTGGAAGCCTTCAA | 64326 |
rs187402806 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175991728 | AAATAGGAAAAAGCT[C/T]TTTAAACTTTTTTGT | 64326 |
rs187428336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176103207 | GCATCTTTTGTTATT[C/T]ACAGCAAGTTCCTTT | 64326 |
rs187428847 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | RFWD2 | GRCh38.p7 | 1:175948728 | TTCCAGAATTTTTAA[C/T]GGAATCAGAATACTC | 64326 |
rs187434670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176065350 | TACTAAGAAGTTTTA[A/G]ATGTCTAAAAATGTC | 64326 |
rs187481956 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176067976 | AAGCCACACCCCCAT[C/T]GCACACCCTGCAAGG | 64326 |
rs187486864 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176046828 | AAGGGGATGGAATAC[A/T]TATAACAGAACCACT | 64326 |
rs187490461 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:175977419 | AGCAATTATAACAGA[C/T]TGACTTTTCTTCAAT | 64326 |
rs187497751 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176105559 | GTGACAGCTAGGTTT[C/G]CATCAGAAAAGGAAA | 64326 |
rs187497959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176146949 | ACTCATTATCCAAAT[A/G]AGTTAAATGAATCTT | 64326 |
rs187499608 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176134629 | AATAAAATTTAACAA[G/T]TTAGGGGGAGAAGTC | 64326 |
rs187508476 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176122915 | TTTGGAAGTAAACTA[C/T]TTCGGTTGGTAGAAT | 64326 |
rs187513058 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176087085 | AACTGGATCCCTTCC[A/T]TATACCTTATACAAA | 64326 |
rs187524384 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176182406 | GTACTTCTCAAGGGA[A/G]GAAAATTTTGTCCCC | 64326 |
rs187529225 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176164694 | GAACAAGAGAAAGAA[A/C]CTGACAATACCACTG | 64326 |
rs187535306 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176198633 | ATACATTAGAAAAAA[G/T]AAAAAACTTTTGCAC | 64326 |
rs187536455 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176136858 | TAGCCAAAGAACTTT[C/T]ACATTACCTCATTTA | 64326 |
rs187537158 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176156234 | GAAGTAGCATACTAT[A/C]AACTGTGTGGGAGAA | 64326 |
rs187539606 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176109005 | CAGTCTCAGCTACTC[G/T]GGAGGCTGAGGCTGG | 64326 |
rs187556378 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176089738 | GTCATGCCCTACAAA[C/T]GATAAAATCTCATCA | 64326 |
rs187568897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176124992 | ATATTTCATTGTAGT[C/T]GTGATTTGCATTTCT | 64326 |
rs187572093 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176141426 | GAATCTCTTGAACCC[A/G]GGAGGTGCAGGTTGC | 64326 |
rs187665804 | snp | A/T | | | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175969462 | GGAAAGGAATGCCCT[A/T]ATCTCTGGAGACAGA | 64326 |
rs187680395 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176072881 | TATTCATTATTTTGA[A/C]CTCCTTATAGGAATA | 64326 |
rs187694919 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176007626 | TGTCAGTGTGCCCCT[C/G]CTGGGGGGTGTCTCC | 64326 |
rs187720997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176108834 | AAAAGATAAAATTGG[C/T]CTGGAGCGGTGGCTC | 64326 |
rs187721022 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176042258 | CCTGGGCGACACAGC[A/G]AAACTCTATCTCAAA | 64326 |
rs187737746 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:175956807 | CTGTAAAATAGGCTC[A/G]GGCAGGTCCTTCAGG | 64326 |
rs187743190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176073532 | GTGGACACTGAACAC[C/T]TAATAGAATAAAAAA | 64326 |
rs187744426 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176051080 | AAAGAATAAGGTAGC[A/C/T]TCACCGGTTTTATAA | 64326 |
rs187750272 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:176033382 | CAGTGAGCTGAGATC[A/G]TGCCATTGCACTCCA | 64326 |
rs187762223 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175996170 | TACCTCAATAGATGC[A/G]GAAAAGGCCTTTGAC | 64326 |
rs187765632 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176170255 | CCTCCCATGAAACAT[C/G]AGTGTTCTTAATGGC | 64326 |
rs187776845 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176204496 | GCCTTGCCTAATCCA[C/T]ATCATCCTACCCCAA | 64326 |
rs187780043 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | RFWD2 | GRCh38.p7 | 1:176136182 | ATAAAAAAAGCATTG[C/T]AGTGGTAATAATTGA | 64326 |
rs187781111 | snp | A/G | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176186061 | ATACATAATAATAAG[A/G]GGACACACCAGCTAC | 64326 |
rs187781631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176028222 | TGAATGACTGAATAA[C/T]AGAATAACATTAAAA | 64326 |
rs187785815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176173360 | CCAGTAATTGGCCAG[A/G]CACAATGGCTCACAT | 64326 |
rs187789462 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176010345 | TACAATGCATCCTAT[A/T]TTCAGATATCTCCCA | 64326 |
rs187798385 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175961035 | CTCCTGGAGCTGGGA[A/C]ACTCTTCTCCTGGCC | 64326 |
rs187798404 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176037285 | GGTGGCGGGTGCCCG[C/T]AGTCCCAGCTACTCG | 64326 |
rs187805115 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:175982140 | TACTAAATACAGAAT[A/G]GCAATATGACCTAGC | 64326 |
rs187805687 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | RFWD2 | GRCh38.p7 | 1:175975479 | CAGTGCCACGATCTC[A/G]GCTCACTGCAATCTC | 64326 |
rs187809727 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | RFWD2 | GRCh38.p7 | 1:175993475 | AACTTAAACCAAAGG[A/C]AAAGAAGTTGAAAAC | 64326 |
rs187818897 | snp | A/G | 1.67688e-05 | 0.00289554 | intron-variant | RFWD2 | GRCh38.p7 | 1:176046143 | TATGCAAATTGTTAC[A/G]TCTATACTGCATCAT | 64326 |
rs187829361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176199170 | AAAATACAAAAAATT[A/G]GCTTGGCATGGTGGC | 64326 |
rs187830882 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176128104 | GTATTTGTATATTTT[A/G]TTCCTTGTATATTTT | 64326 |
rs187840292 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175954931 | TTCAACATTAAAAAA[A/T]ATATATATATAATTC | 64326 |
rs187841013 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176164982 | GGTGACATATACAAT[A/G]AGACAATGCTGAGAA | 64326 |
rs187845450 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176199083 | AGCACTTTGGGAGGC[C/T]GAGGCGTGGGGACCA | 64326 |
rs187887951 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175960329 | TGAATCTCAGTCTCC[A/G]TAACTATAAAACAAT | 64326 |
rs187934719 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176027742 | GTAATACATTAGTAA[A/T]TGCTTCTGTAACTTG | 64326 |
rs187958625 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | RFWD2 | GRCh38.p7 | 1:175995625 | TACAAACACCTCTAC[A/G]CAAATAAACTTGAAA | 64326 |
rs187972543 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176067131 | ATTAGTCCAAACCCA[G/T]AGAATATACAATACT | 64326 |
rs187974003 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176024111 | AGAAATACAAAAAAT[C/T]AGCCAGATGTGGTGG | 64326 |
rs188007974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176062473 | ATGCCTGATATTTAA[A/G]AAAAATAACAATGCT | 64326 |
rs188010319 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175955783 | ACACACACACACACA[A/C]ACACACACACACACA | 64326 |
rs188032659 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176051587 | TACTTATTTTAAAAA[A/C]AAACAAACAAACTGT | 64326 |
rs188053715 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176016007 | ATACATGGCTTGGAC[A/C]ACTGCATCAACAGGA | 64326 |
rs188060659 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | RFWD2 | GRCh38.p7 | 1:176090256 | AGATCGAATCAATGT[A/G]AACTTCCTAAGTAAT | 64326 |
rs188068338 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176150505 | GCTCTGTCTCAACAA[C/T]GACGACAAAGCATCC | 64326 |
rs188069654 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176117665 | TTTGGGAGGCCAAGG[C/T]GGGCGGATCACCTGA | 64326 |
rs188096229 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176147531 | ATATCCAGAAGTATT[G/T]GGAACTAGTATGTTT | 64326 |
rs188102145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176115002 | GAAAAGAAATTATAC[A/G]CATATATAGGTAAAA | 64326 |
rs188139385 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176209198 | TTCAGTGTTTTAAAA[A/C]ATATATTAGTGACTA | 64326 |
rs188159995 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176154157 | TTGGAATAGTTTCAG[A/T]AGGAATGGTACCAGC | 64326 |
rs188171548 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176120573 | TCTTGCTGGTAACAG[A/T]GAGAAGCTTTGCTAA | 64326 |
rs188175449 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176134493 | ATGACAAATATAACC[C/T]TATACTAATATCGCA | 64326 |
rs188181074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176186956 | CACAGCTCCATCATC[C/T]GTTAGTTTATTTAAA | 64326 |
rs188181818 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:175981545 | TTAGAGGCTTAAACA[A/T]AAGACTGAAAACTGT | 64326 |
rs188184298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175950466 | TAGCATAGAGATGTG[A/G]AAGTGGTACGTACAA | 64326 |
rs188190666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176171189 | ATCTGTCATTTACTA[C/T]AGCCACCTTCAACAA | 64326 |
rs188191412 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176128456 | TTACTGACTTTGGCA[A/T]CAAGTTCAACTCCTT | 64326 |
rs188194866 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176205427 | CTAATCAATAACTTT[A/C]CTAACAGTTCCAACT | 64326 |
rs188201551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176070481 | AGCCTGGCCAACATG[A/G]CGAAACCCCGTCTCT | 64326 |
rs188214555 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176115342 | GTAGTCCCAGCCACT[C/T]GGGAGGCTGAGGCTG | 64326 |
rs188228901 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176009800 | GGAGACAGGGGCATA[C/T]GAAGATGGTCTACAC | 64326 |
rs188247134 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176005045 | GCCTGTTATTGGTCT[A/C]CTCAGAGATTCAATT | 64326 |
rs188249315 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176086518 | GGCATGAGCCACTGC[A/G]CCTGGCCTGATTTTG | 64326 |
rs188264075 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176044828 | ATTCCAATATATCAG[A/G]AAGTATTGCACATTT | 64326 |
rs188282102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176000816 | TCTAGTGTATCATTT[C/T]AGTTTGAGTATATTT | 64326 |
rs188297545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176185863 | AATCCAAATCCTTAC[A/G]GATGATACAATGACA | 64326 |
rs188298963 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:175976590 | GCCTCATTTATTCCT[C/T]CTTATTAGTTGCTAT | 64326 |
rs188326572 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176034451 | CGAATATGAAAAAGG[C/T]GAATCCCCATTATAT | 64326 |
rs188328109 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176102268 | ATTTTTCCCTTTTTC[C/T]TTTTCGCCCAATAAA | 64326 |
rs188336855 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176130692 | AACTGTGAAAATTAA[A/G]TGACATTCTAGGTTA | 64326 |
rs188348898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176109170 | TTGAAGCAATTAAGC[C/T]ATTTACTTGCCCTAA | 64326 |
rs188350300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176022315 | GGATCCACAGTGCCC[C/T]TGCAACAGGAAGTCA | 64326 |
rs188359616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176074000 | GCAGTGATCTCAGCT[C/T]ACTGCAACCTCTGCC | 64326 |
rs188387360 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176059966 | CTCGCAGGTATTAGT[C/T]TGCTGACCTTAAACT | 64326 |
rs188391641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176040112 | TGGACTTCTTCAAAA[C/T]GAAAACAATTTTGTG | 64326 |
rs188400218 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176208319 | CAAAAAATTAGCTGG[A/G]CATGGTGGCAGCAGG | 64326 |
rs188401899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176116164 | AGACAGATCGCTTGA[A/G]TCCAGGAGTTTGAGA | 64326 |
rs188406068 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176157674 | AGTAACTTAACTACA[G/T]GTCAGGACAAAGTTC | 64326 |
rs188413845 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176035340 | TAGAAGACAGAACAA[C/T]ATAAATTACCCAACC | 64326 |
rs188415613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175969133 | TTAACAGAAAAAGCA[A/G]TACATTCAAGGCATG | 64326 |
rs188418469 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176123480 | GAAAAGAGTTTCCTA[C/T]GTGACTCTAAATGAC | 64326 |
rs188418588 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176079836 | CTCTCCATTTTCCTG[A/T]ATAAATTTTCATTAA | 64326 |
rs188419222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175989027 | CTCATTCTATTGCAT[C/T]AACTATGTTGTTTAT | 64326 |
rs188420619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176097402 | AGGCCTTAGAAGCTG[A/G]ATGTTTTCCTAGCCC | 64326 |
rs188422560 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176137417 | TTAAAAATAAAATTA[C/T]TCAATCAAAAGAAAA | 64326 |
rs188423415 | snp | A/G | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176016485 | GAGAAGAATTTCTAT[A/G]TAAGGGTAGGAGCAG | 64326 |
rs188429297 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176001288 | CTGGATTCATCGAAT[A/G]AACCTCTAGGCATCA | 64326 |
rs188432550 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176174961 | TTCACAGTTGGTTCT[A/G]ACTAGTTATTATTTC | 64326 |
rs188436546 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176208740 | TCGGAAACTGGACAG[A/G]AAGTTGCTGGGCAGA | 64326 |
rs188443384 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176074563 | TATATTAGTCTAAAT[A/G]TTTTAATCTAACCAC | 64326 |
rs188446079 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176191155 | TATAGAATATTACTA[C/T]ATCCCAATTTATACA | 64326 |
rs188451259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176052350 | TCAGAATGTATTTCC[A/G]TCGTTAAGCAATGCA | 64326 |
rs188487547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176038174 | AAATACCATTTTCAT[C/T]AGCACCAAAAAATAA | 64326 |
rs188510100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176114261 | TGGTATTTTCATGAC[C/T]GTTCAGAAACAGATA | 64326 |
rs188514224 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176077547 | CACAGCCAACTTAAT[A/T]GTGAATGGGCAAAAG | 64326 |
rs188566702 | snp | A/G | 0.0020555 | 0.0319925 | intron-variant | RFWD2 | GRCh38.p7 | 1:176168680 | CTGAATCAGCCTTTC[A/G]GGATCAGGAGAGGGA | 64326 |
rs188576192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176203569 | GTCTAGTTAAATGAA[C/T]CGTAAGAAAATTTTG | 64326 |
rs188601431 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | RFWD2 | GRCh38.p7 | 1:176008050 | ATAATCTCGTGGTGC[A/G]CCGTTTTTTAAGCCG | 64326 |
rs188608118 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176159482 | TTAATAAGATTAAAA[A/T]GTGCACACATACCCT | 64326 |
rs188612415 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:176132036 | TTACGAGATCTGCTA[C/T]TTTATTTTACAATAC | 64326 |
rs188621832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176064215 | ATAAAAACAAACCCA[A/G]TGTAAAGTTTGAAAA | 64326 |
rs188626455 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176101109 | CAGCAGGGGACATAA[C/G]GTGTACATGGGTAAG | 64326 |
rs188628553 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176194046 | ACACTATTGCAAAAT[G/T]TTTATATTGTATATG | 64326 |
rs188635808 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176042764 | AAAAAGTGGCTCACA[A/T]CTGTAATCCCAGCAC | 64326 |
rs188643756 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176025053 | GCAAGGTTCATTCAA[C/G]AAAAATACAATTCAG | 64326 |
rs188664606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176190839 | TGCTAACTCCATTAT[A/G]CTTTCATAAAATGTG | 64326 |
rs188672257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175962758 | CATCTCTCACCGCAC[C/T]TCCCCCTCCCTGGGC | 64326 |
rs188682641 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175967991 | TCCTGTCTCAGCCTC[A/T]CAAGTAGCTGGGATT | 64326 |
rs188699879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175966982 | GATTTCTTCATCACA[A/G]AGGAACACTTTCAAA | 64326 |
rs188763278 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176055063 | TCTCTTCCACAATAG[A/T]GTGATTTTTCTCCTA | 64326 |
rs188764428 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176000637 | AATGTAAATATTTTT[A/T]AAAAAATGAAATCCA | 64326 |
rs188779657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176019679 | CACCCTGGGTAACAT[A/G]GTGAAAATACGTTTT | 64326 |
rs188786993 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176095420 | TGGTGTGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 64326 |
rs188806914 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175991501 | GCCTAAGACGTTAAC[A/C]GTATACCTAGGCTAC | 64326 |
rs188823942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176019063 | CCCAGCTACTTGGAA[A/G]GCTGAGGCACGAGAA | 64326 |
rs188827627 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176127355 | CTTCTCCCCTCTCCC[C/T]ATCCACCTCTAATCT | 64326 |
rs188835376 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176156751 | TCATCCAGAAGATAT[A/T]AAAATTCTAAACATG | 64326 |
rs188852414 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176119463 | AATACTCATCAGTTT[C/G]TTGAAGATAAAACTA | 64326 |
rs188853644 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176122713 | ACCTAATACTTATAC[C/T]GCCTTTTAAAATGTT | 64326 |
rs188861127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176101717 | CTTATTTTGTTTTGA[C/T]ACATGTTTTCTAATA | 64326 |
rs188863129 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176083666 | CCAAAGTAATAGTTC[C/T]TTAATATTCATCTTT | 64326 |
rs188868698 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176086610 | TCCAACGAAATAAGA[G/T]GACACAAACAAATGG | 64326 |
rs188918715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176178931 | AGTCATCCTAGCACT[C/T]TGGCAGGCCAAGGTG | 64326 |
rs188927134 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176151325 | AGAAAGAAAGAAGGA[A/G]AGAAAGAAAGAAGGA | 64326 |
rs188941628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175948051 | TGGGAAAAAGGACTA[C/T]CTTTCTTTTTAATTA | 64326 |
rs189007505 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176015006 | ACAATGAGACAGAGA[A/G]GAAAGGTAATGACTG | 64326 |
rs189022696 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176163071 | TTTACTTGCTACTTC[C/T]TAATATGCTCATTAC | 64326 |
rs189035268 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175987632 | ATTTTTATTTTTGAG[A/C]CATCTATTAAAGATA | 64326 |
rs189037811 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992416 | AGTGGGTGCAGCGCA[C/G]CGTGCGCGAGCCAAA | 64326 |
rs189039468 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176181462 | ATAGCAAGCCTGATG[A/T]TGGAATTGACAGCCT | 64326 |
rs189039692 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176144906 | AGATAAAAGAATAAA[A/G]CTTCAAATAAAGAAC | 64326 |
rs189039749 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176010948 | TTTCCTCAGTGGTGG[C/T]AGGAGCCTGAGGACA | 64326 |
rs189042557 | snp | C/T | 0.00716266 | 0.059414 | downstream-variant-500B | RFWD2 | GRCh38.p7 | 1:175944767 | TTACATTATAGTTCA[C/T]ATATGCTACTTCTTA | 64326 |
rs189055367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176195299 | GATCAATTCACCAAC[A/G]CTAAATCTGTGTAAG | 64326 |
rs189066496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175952516 | TTCAGATAAAATAAA[A/G]CTGAGATAATTTTTC | 64326 |
rs189072805 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176006030 | TATGAGTCTGGGTGC[C/T]CTTGTATTGGGTGCA | 64326 |
rs189074709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175973835 | CATATGTAACAAACA[A/G]AAGTGCAGGAAAGGG | 64326 |
rs189075358 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176087600 | CATTAAAAAGTCAGG[A/G]AACAACAGGTGCTGG | 64326 |
rs189077021 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176029411 | GCCATTTTACAAAGG[C/T]ACCAGAGCAACTATC | 64326 |
rs189079763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176139213 | ATAAATGTTAACAAA[A/G]ACCAAAATGAGATAC | 64326 |
rs189083141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176184285 | AGCCTGCTTCACTGC[A/G]TTCTCCAACCTATCC | 64326 |
rs189095521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176166153 | ATTTATTGAGACAGG[A/G]TGTGACTCTGTCACG | 64326 |
rs189096233 | snp | C/G | 0.021333 | 0.101051 | intron-variant | RFWD2 | GRCh38.p7 | 1:176004500 | GGTTTGTCATAGATA[C/G]TTCTTATTATTTTGA | 64326 |
rs189099784 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176199840 | CATATCTTCATTAGG[A/G]TGGTGACTGCACAGG | 64326 |
rs189113972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176067603 | CCACTCTATCCTCCT[C/T]CTGGCCTCTCCATCA | 64326 |
rs189114707 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176158446 | CAATCTAGACAAAAG[A/C]ATAAAGGACACCAGA | 64326 |
rs189121154 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176124079 | TGAACTTTTATCATC[A/G]TCATCAAGCAGTGAT | 64326 |
rs189135014 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176157983 | CAAAGTGGAAGAGGG[G/T]ACATAAAAATATTTG | 64326 |
rs189143111 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176192207 | TCTTCCTGGATTTTA[C/T]TCCATTCACACACTC | 64326 |
rs189154763 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176105329 | GTAAATGAACCTAAC[A/T]GTATTTCAAAGAAAT | 64326 |
rs189173347 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176179979 | AATCAAAGTATATCA[A/C]ATTACATACCACTGT | 64326 |
rs189231400 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175972381 | TAGTGAGAGGGAAGT[A/G]AGGAGGAAAGAATTT | 64326 |
rs189276254 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:175979228 | TGGGTCTAAAAATAG[A/T]ATTGTTTTGTTAATT | 64326 |
rs189278938 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | RFWD2 | GRCh38.p7 | 1:175994065 | CAGAAACTCTACAAG[A/C]CAGAAGAGAGTGGGG | 64326 |
rs189298564 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176008686 | ACTATGTGGCAACTG[A/T]GGACTCGGTTCTTCC | 64326 |
rs189301010 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176024402 | ACAATCAACCTCAAC[A/G]GAGGCAAAAAAAAAG | 64326 |
rs189301660 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176075331 | TTTCTTTAGCTAATG[A/G]CTTAAATTTTAAGAT | 64326 |
rs189303751 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | RFWD2 | GRCh38.p7 | 1:176091723 | CCAGAAGAGGGATGG[C/T]GGGGGAGGTAAAAAC | 64326 |
rs189307989 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:175957598 | ACCAATGAATGTAAT[A/G]CAACAACTATGGAAA | 64326 |
rs189311307 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176007967 | GCCTTGCAGTTTGAT[C/G]TCAGACTGCTCTGCT | 64326 |
rs189316716 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176053548 | TTGACTTCCTCTTCT[C/T]CAAAGATCTTTTATT | 64326 |
rs189319123 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176126398 | GTGTTCCTTCTATAA[C/T]CAGTTCATTGAAGGT | 64326 |
rs189319453 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | RFWD2 | GRCh38.p7 | 1:175978426 | AGAGGCTGTCCACAC[A/G]GTAGTGGACATTAAG | 64326 |
rs189330032 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176043423 | ATAAGATGTTGATAT[A/C]AAGTACTTCCAAAAC | 64326 |
rs189331262 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176144212 | ATAGAAAACATACAA[G/T]AATCTACAAATAAAT | 64326 |
rs189333329 | snp | A/G/T | 0.00279242 | 0.0372774 | intron-variant | RFWD2 | GRCh38.p7 | 1:176111779 | GCCAGGCTTATACTC[A/G/T]ACTATCCACTATTTC | 64326 |
rs189354127 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176142814 | GAAAATTAGAAATTA[C/T]TTTGAACAATAATAA | 64326 |
rs189362553 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | RFWD2 | GRCh38.p7 | 1:176084587 | AAGCACAATAAGGGG[C/T]TCCATTCCCAGGCAA | 64326 |
rs189363447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176110133 | ACACAATGCAGACGA[C/T]ACTATTTATCTTGTC | 64326 |
rs189364259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176161275 | GAGCAAGGTAACTGC[A/G]TATGTTCAATCTCTC | 64326 |
rs189365118 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176106883 | TGACTAGCTCACAAT[G/T]AGAGACTCCAACCAA | 64326 |
rs189385644 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176137798 | TAGTATCTTCTGTGG[C/T]AATACAGGCAAAGTT | 64326 |
rs189389970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176030109 | GATGCACACCACCAC[A/G]CCTGGCTAATATATT | 64326 |
rs189407729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176106006 | CTTTGGGAGGAACTT[A/G]GTTTACAGGTTTGTT | 64326 |
rs189411018 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176175628 | TCCTGCTGTGCAGCC[A/C]AGTTCCTAATAGGCC | 64326 |
rs189415986 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176069224 | AAAAGAAATTATATG[C/T]AATACAGTAATACGT | 64326 |
rs189439474 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176206136 | CTCCACCCCTCTGCA[C/T]CCGAGGAAGCTTAGT | 64326 |
rs189459152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176129559 | GTATTTTGTACTACA[C/T]TTATTTACTACCTTA | 64326 |
rs189464936 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176166721 | GCAGGCAAACAGCTT[C/G]AGCCAGGAGCTGGAG | 64326 |
rs189470441 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:176160319 | AGTGCAGAATGTGTA[G/T]GTTTGTTACCTAGGC | 64326 |
rs189472521 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:176194527 | CCTATAATCCCAGCT[A/G]CTAGGGAGGCTGAGG | 64326 |
rs189537312 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175997581 | ACCCCATGAAAAAGT[C/G]GGCGAAGGGAATGAA | 64326 |
rs189540283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175964286 | CCTCTACCCTTAGAT[A/G]TTTAAAAGCATAACC | 64326 |
rs189544042 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176048899 | AATTAAGGGCCGGGC[A/G]CGGTGGCTCACGCCT | 64326 |
rs189545902 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176096677 | TGAGAGGATTTTTTT[C/T]TTCCTTTTTAGAAAA | 64326 |
rs189548105 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176078922 | TCATCAGAGAAATAA[A/T]AATCAAAACCAGGAT | 64326 |
rs189548130 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176031069 | TTAGGAAGGAGACAA[G/T]AAATAATTTTTCCCC | 64326 |
rs189553825 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175984377 | TGGTGTTGAGCCTGC[A/G]TGTGCACAGAAATAA | 64326 |
rs189557992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176011614 | CAAATTGTCCAATTA[C/T]TCAAAATGTGAGCTT | 64326 |
rs189560135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175997662 | AATGCTCATCATCAC[C/T]GGCTATCAGAGAAAT | 64326 |
rs189571181 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175994989 | AAATTGACCACATAG[C/G/T]TGGAAGTAAAGCTCT | 64326 |
rs189585630 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175958097 | TAACTGAATTAAGGT[A/T]GTAGTTATACTGATG | 64326 |
rs189606172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176091187 | GAAGTTTATTACCAG[C/T]GAGCCATCTCTAAAA | 64326 |
rs189611329 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176064963 | AGCTACCACTTCTTG[C/T]TGTTGCCGTTTAACC | 64326 |
rs189622973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176014077 | TATCTTCATGTTTTT[A/G]GTGGAGAATAAAGGG | 64326 |
rs189623837 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176026215 | ATTCATATCTGGCAT[G/T]GGTACAAATTAATTA | 64326 |
rs189644190 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176073035 | CTAGAATTCAGGTAC[G/T]CCTGTATCCAAATCT | 64326 |
rs189645826 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176097801 | TTGAACATGGGAAGC[A/G]GAGGTTGCAGTGAGT | 64326 |
rs189648344 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176117133 | AATCAATTACTCAAG[C/T]TTCCTCATCTGTAAA | 64326 |
rs189651640 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176000316 | CCATTCTTCTGCAAA[C/T]GGATATCCAGTTTTC | 64326 |
rs189654467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176126144 | AGGTTTTTCCAAATA[C/T]AAGATCACATCATCT | 64326 |
rs189657646 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176050241 | GTAGGAAACTAGCTG[C/T]ATTCTTTGTCAAAAA | 64326 |
rs189660469 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RFWD2 | GRCh38.p7 | 1:176033166 | CCTGTAATCCCAGCA[C/T]CTTGGGAGGCCGAGG | 64326 |
rs189665183 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175994681 | AAAGAAATCAATTCA[A/T]CAAGAAGAGCTAACT | 64326 |
rs189665333 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176047299 | ATTTTGCATGTATTA[C/T]CTCATTTAGTCCTCA | 64326 |
rs189668539 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176149746 | CAAAACATAAAAACA[A/C]AAGTATGTATCATTT | 64326 |
rs189677963 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176011247 | AAATTAAACTAAAAC[G/T]TACTTTCTCAGTAGA | 64326 |
rs189680113 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | RFWD2 | GRCh38.p7 | 1:176168049 | TTAGAGAGGTAAGAA[A/C]ATTCAATTTACGATT | 64326 |
rs189687147 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176129855 | TGCAATGGCTTTGAC[A/G]AGAATTTAAAATCTA | 64326 |
rs189688029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176201487 | GTAACAGTTCTTAGA[C/T]GGAACATATCCACCT | 64326 |
rs189695085 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176087148 | TTAGACCTAAAACCA[C/T]AAAAACCTAGAAGAA | 64326 |
rs189695563 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176184845 | GAGATGAAATTTCTA[A/T]TGAACTAAACTTTAG | 64326 |
rs189712310 | snp | A/C | 0.0170251 | 0.090679 | intron-variant | RFWD2 | GRCh38.p7 | 1:176202674 | CCCTGTCTCAAAAAA[A/C]GGAAAAAAAAAATTG | 64326 |
rs189737568 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176092982 | AAATTGTAGTATAGT[A/C]ACACAATGGAATATT | 64326 |
rs189744025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176149093 | CAATAGAAAATTATA[A/G]TTTTTCTTTTAAAAA | 64326 |
rs189803717 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:175983904 | ATGAGTTAGGGTATC[G/T]GGTAGAATAAATTTC | 64326 |
rs189863871 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176018837 | AGATCACACCACTGC[A/C]CTCCAGCCTGGACCA | 64326 |
rs189877091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176122343 | CCATCAGTTTTATAC[A/G]ATACATGGCATATGT | 64326 |
rs189881226 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176136124 | CTCTTTTAATTAACC[G/T]TAACTCCTAGAAATG | 64326 |
rs189890004 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176076673 | ACAAAAGATAAATAA[G/T]ACCAAGAGTTGGTTC | 64326 |
rs189892027 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175991298 | TGTATCATGTTACTG[G/T]ACTGAATGCTGTAGG | 64326 |
rs189893657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176054408 | CTCAGGTGATCTGTC[C/T]GTCTCAGCCTCCCAA | 64326 |
rs189900479 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176002535 | CAACAGTCCCCAGAG[C/T]GTGATATTCCCCTTC | 64326 |
rs189908171 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176036980 | TGTCAAAAATTACAC[C/T]CAAGAAGAGACAGAT | 64326 |
rs189912589 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176189516 | TCAAAATGAAAGCAA[A/G]TAAACTCATTTTCAA | 64326 |
rs189913405 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176153678 | GTGTTGGTTTTCAAG[G/T]GCAATGCTTCCAGCC | 64326 |
rs189917018 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176156011 | AATATTTGGGTAAAT[A/C]AAAAAAGGGTCTGGT | 64326 |
rs189918676 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176172986 | CTGAAAGCTGCACTA[A/G]AGATCACCGTCAAGA | 64326 |
rs189919908 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant | RFWD2 | GRCh38.p7 | 1:176006406 | ATGATGTTAGCTGGT[G/T]ATTTTGCTCGTTAGT | 64326 |
rs189921530 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176126753 | CACTGCACCTGGCCA[A/T]CAACATCACTTTTTA | 64326 |
rs189922620 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175978839 | TCTTCTCCGCACTCA[A/C/T]TGAGGAATTTAAAAT | 64326 |
rs189923129 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207920 | TAGCAAGTGTTACCA[A/G]TTTTATTAGTTCGAC | 64326 |
rs189929860 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176092479 | AGATATTTGCAGTAT[C/T]CAAAAACAAATGATT | 64326 |
rs189941889 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992579 | GGCTTAAAAAATGGC[A/G]GACCAGGAGATTATA | 64326 |
rs189944481 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176186343 | AGACCTCATCTCTAC[A/C]AAAAAAAAATTAAAA | 64326 |
rs189951902 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:175965674 | GCTCACTGCAACCTC[C/T]GCTTCCCGGGTTCAA | 64326 |
rs189955856 | snp | A/G | 0.000237063 | 0.0108846 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176184744 | AAGTAGAGTGATTAC[A/G]AATTGGAAAAGACTA | 64326 |
rs189958343 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:175986775 | TGCTCTATTACTATG[C/T]ATTTCAATCACTACC | 64326 |
rs189996413 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | RFWD2 | GRCh38.p7 | 1:175959337 | TCTACAAAACTCTTA[C/G]AGCAGACATACTTAA | 64326 |
rs190038289 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176176483 | GTCACAAAAAGCTGA[C/T]TTAAAATTATATACT | 64326 |
rs190112817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175982689 | GCCTCTTGCCCCCAC[A/G]TTGTCAAGGTTAAAC | 64326 |
rs190115182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175962408 | ACCATTAGTTTCTTA[C/T]ATATTAATATTTGCC | 64326 |
rs190139467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176079484 | GGACAACTAGATGGG[A/G]AGGTGGGAGAGGGCA | 64326 |
rs190153903 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176076202 | TGGAACATGTTTTAA[A/G]ATAGACCACATGCTT | 64326 |
rs190156590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176039465 | AAAATAGATGAATGA[A/G]AACAAGAAACCACAT | 64326 |
rs190161278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176002159 | AATACTGGCCATCAT[C/T]TCTACAAATATTTTC | 64326 |
rs190166546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176115609 | AAAAAATTAGCTGGG[C/T]GTGGTGGCGCGTGCC | 64326 |
rs190183948 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176170573 | TCAACAGTGGTCTTA[C/T]GATATTCAGTAAATC | 64326 |
rs190185489 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176133404 | CTCTTTATGTGCTCT[A/C/G]TTATTTTCTTATGAG | 64326 |
rs190185653 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | RFWD2 | GRCh38.p7 | 1:176112002 | AGCACACATGTACCA[C/T]GCATACAGTGAATCA | 64326 |
rs190188347 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175945980 | GTCAGTGGGATCCTA[A/T]GAGAACCTATGTAGT | 64326 |
rs190192830 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | RFWD2 | GRCh38.p7 | 1:176035615 | ATAGTTTCAAAATAT[A/G]TCAGGTAAAAACACA | 64326 |
rs190192990 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | RFWD2 | GRCh38.p7 | 1:176063585 | CCACAAAATCACCTA[C/T]TGATGTGGATGGGGA | 64326 |
rs190196520 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175971267 | TTCTCCAAAAACTCA[A/C]TGCCTGATTTAAATT | 64326 |
rs190202284 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175990106 | ACAATTCTCTATCAA[C/G]ACTGCTTTGGCTGAT | 64326 |
rs190210387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176205183 | AAGACAACTAAATTA[C/T]GCACACCCCACTTTG | 64326 |
rs190215809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176001724 | TGGACTTACATTACA[A/G]TCTAGTATCCCTTTA | 64326 |
rs190276633 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176192550 | TTCCAATTCCTAAAA[C/T]ACAAAATATAATTGG | 64326 |
rs190277565 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176194781 | CCATGTAAACACTTA[C/T]GAAAAGAAAGCTAGG | 64326 |
rs190304240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176182489 | ATGGGCAGGGGTGGT[A/G]CTGGGTAGGGGTCAA | 64326 |
rs190319329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176198743 | TGTATGCAGAATACA[C/T]AAAGAACACTTACAA | 64326 |
rs190347500 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175969521 | TCTTGCTAAGTTGCC[C/G]CCAGTTTATTACCAT | 64326 |
rs190348735 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:176130877 | ATCAAAATAAGTAGA[A/G]ATCTTTACAAAACAA | 64326 |
rs190358994 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176139445 | AACTACTATTTGACC[A/G]AGTAATTCCATTATT | 64326 |
rs190363157 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176177348 | TATGAGAAAAAAATA[C/T]TAAAAAAAAAAAAGA | 64326 |
rs190365754 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176158913 | CCCAAAGTGCTAGGG[A/T]TACAGGCGTAAGCCA | 64326 |
rs190367462 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176117679 | GCGGGCGGATCACCT[A/G]AGGTCAGGAGTTCGA | 64326 |
rs190367984 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176021779 | GCTGTCAAAATCATT[G/T]AGAACCAAGTCTGAT | 64326 |
rs190374834 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:175996199 | ACAAAATTCAACAAC[C/G]CTTTGTGCTAAAAAC | 64326 |
rs190380016 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176193314 | GAACCCTTATACATT[G/T]CTAGTAGGAAAATAA | 64326 |
rs190386935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175951321 | TGAGAAATGAACAGT[C/T]ATTCACTCAGCAACT | 64326 |
rs190403900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176059639 | AGGTGCACACCACCA[C/T]ACCTGGCTTATTTTT | 64326 |
rs190408817 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175992076 | CTAGACTTTTTGAAC[A/C]TTTTTAATTTTTTTT | 64326 |
rs190421738 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176128861 | AAGCATTAACATGAA[A/G]CAGCAGACATTGACA | 64326 |
rs190425084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176097057 | TCTTTGAGCCTTTAG[C/T]AAAGTTTGAAAGCCA | 64326 |
rs190439427 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176082737 | TTGAACCCGGGAGGT[A/G]GAGGTTGCAGTGAGC | 64326 |
rs190447609 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176021358 | CCTCTAAATGGCCTA[C/G]TTTGCTAAGATTGTA | 64326 |
rs190448222 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | RFWD2 | GRCh38.p7 | 1:176016741 | ATGACTCTTTTTTTA[A/T]AAAAAAAAATTACAG | 64326 |
rs190456079 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176042550 | CCTGGGCAGCAGAGC[A/G]AGAATCCGTCTCAAA | 64326 |
rs190475546 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176057176 | ATCTTATTATCCATT[A/G]TATTGTCTAATGCAG | 64326 |
rs190531992 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176180502 | TCTCGGGTCCACCTG[A/C]GAAATTTTCAAGCTA | 64326 |
rs190545914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176027393 | AGTGACAGAATAGTG[C/T]AATTAAGGTACAGCA | 64326 |
rs190561595 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176203116 | GCAGAGGCGGGCGGA[C/T]CATGAGGTCAGGAGA | 64326 |
rs190572378 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176185343 | CAGCTAAGAAGTAAC[A/G]AAGTCAAAATTCAAA | 64326 |
rs190572939 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176086047 | TATTTTCCAATTTAT[A/C]TTTTAACATGAAAAT | 64326 |
rs190575792 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176066759 | CCTTCACCAAAAAAT[A/G]ATAACTAGAACAGCT | 64326 |
rs190583165 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176044427 | ACATATCTGCATCAC[A/G]CATATAGTAAAGGGA | 64326 |
rs190589898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176193718 | AAAAGACCATATATT[A/G]TATGATTGCATTTAT | 64326 |
rs190590610 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:175945526 | GTATCCTTGTTTAGG[A/T]TTTTAATCTGTTTTC | 64326 |
rs190593687 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176135803 | CTAGCTAATGCAACC[G/T]CAGCTCAATCATACA | 64326 |
rs190604863 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176104256 | TTTAAGAAACAAGGG[C/G]TTTCTCTACATCCTG | 64326 |
rs190606599 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | RFWD2 | GRCh38.p7 | 1:176122032 | GTAGTCCCAGCTACT[C/T]AGGAGGCTGAGGCAG | 64326 |
rs190650245 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176108407 | CATATGATTAATACC[A/G]GTATACAATCTTTAC | 64326 |
rs190650810 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:175973772 | ACTCTAATATTTTTG[C/T]GGCTACAAAACTCAG | 64326 |
rs190658419 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176124497 | ATTGATTTTTAGATC[A/C]CACAAATAAGTGAAA | 64326 |
rs190683852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176060252 | TACCTGATAGACTAT[A/G]TTCTGAAAAACTTTT | 64326 |
rs190701698 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176023103 | TGTTCTTGATTTCAA[C/T]AGTGCCACTAGCTGA | 64326 |
rs190704516 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176005756 | TTACATTTGCTGAGA[A/G]CTTTACTTCCAACTA | 64326 |
rs190745519 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176124854 | CCAAACCATTCTCCA[C/T]AGTGGTTGTACTAAA | 64326 |
rs190756557 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175955120 | GGTGTGGTGGCATGC[A/C]CCTGTAGTCCCAGCT | 64326 |
rs190759459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176188341 | ATGAAAAATCTCAGA[A/G]ACTACAGAAATGAAG | 64326 |
rs190759923 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176159325 | CTGTACTGGTTATTA[C/T]AGAAATGTATTTTTA | 64326 |
rs190781521 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | RFWD2 | GRCh38.p7 | 1:176113971 | TTTTTATAGTTTGCA[C/T]AGTGACCTTGTTTTT | 64326 |
rs190782635 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176113172 | CATTCTCATCAGTAT[A/G]GGGGCATTCACTCTT | 64326 |
rs190789413 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RFWD2 | GRCh38.p7 | 1:176094364 | TGCCAGTTTAATTAT[C/T]AAATTATAAATAATA | 64326 |
rs190790653 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176086578 | AATAATTATCAAATA[A/G]AAAATGAGTTACTTT | 64326 |
rs190791494 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176077288 | TCCAGGAGCACATCA[A/C]AAGTTAATTTGCCAC | 64326 |
rs190816973 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175976042 | CTCAAAAATCCAGTA[A/T]TATGTAAAAGATGTA | 64326 |
rs190818815 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176041678 | TTTTTAAAAAAATAA[A/T]CAGTAGGCCGGGCAT | 64326 |
rs190820988 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176088187 | CCAGCAAACCAACAC[A/G]GCACATGTATACATA | 64326 |
rs190826447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176145749 | AAGATTACATACTGC[A/G]CAAGCACACTTAAAT | 64326 |
rs190826874 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175993502 | AAACTTTGAAAAAAA[C/T]TTAGACGAATGTATA | 64326 |
rs190827169 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176023138 | TAACAGCTCTCCTGG[A/C]CTATCTGATGATGAG | 64326 |
rs190828862 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176071394 | CTCTTTATAAATTAC[C/T]CAGTCTCGGGTATTT | 64326 |
rs190840491 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176181632 | CGGATCACAAGGTCA[C/T]GAGATCGAGACCATC | 64326 |
rs190861685 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176043949 | ACAATCATTATTCTG[C/T]CCACAACATACCTGG | 64326 |
rs190863768 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:175959659 | TTAAGGACTACCTAG[A/G]TACCTTTCTCTTATT | 64326 |
rs190871463 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175979954 | ATTATGTACAAACAC[A/G]CTGTGTAATGCTAGG | 64326 |
rs190874169 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | RFWD2 | GRCh38.p7 | 1:176026765 | ATGGTGCTAACTTGT[A/T]TTTTTTTTTGTAAAA | 64326 |
rs190879979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175995071 | CAGCGCAATCAAACT[A/G]GAACTCAGGATTAAG | 64326 |
rs190882164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176008997 | GCCTTCACTTCCTGC[C/T]TACACAGAGCTCATG | 64326 |
rs190887288 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175947348 | CAATTCCTAAGACAA[C/T]TGAATCTAATATGAA | 64326 |
rs190942746 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176041118 | AGAGATTTTAGTATA[C/T]AATAGAAATTAAATA | 64326 |
rs190982704 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | RFWD2 | GRCh38.p7 | 1:176080798 | TTCTGGAAGCTTCAC[C/T]GGCAAATTCTACAAA | 64326 |
rs190983281 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175999736 | CCACCACCACTGTAC[A/G]AGGGTTCCCTTTTCT | 64326 |
rs190985098 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176108858 | GTGGCTCATGCCTCT[A/C]ATCCCAGCACTTTGG | 64326 |
rs190989560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176146056 | ATTCAATTCACTAAA[A/G]TTCCAAGTAAAACCA | 64326 |
rs191001914 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176164554 | CTATCTTTCAGAAAG[A/G]AAAGGATAGGAGAAA | 64326 |
rs191003992 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176127291 | TTGCACAACAGAACA[C/T]CAGAATTGATTCTTC | 64326 |
rs191007586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176032287 | GTGTATTGTTTTATA[C/T]CTCTATAAAAAGTAT | 64326 |
rs191018804 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176178614 | TCCAGCACTATGGGA[A/G]GCCAAGGCCGGCAGA | 64326 |
rs191020695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176140383 | CTATCCGTAAGAAAG[C/T]CTGACAAGGTATCAG | 64326 |
rs191034085 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176197608 | AAAAATTAAAAGAAA[A/T]TCACAGACCAGTATC | 64326 |
rs191035654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176067136 | TCCAAACCCATAGAA[C/T]ATACAATACTAAGAG | 64326 |
rs191039471 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176126955 | TCTATTTACACCAAA[A/C]TTTAAAGAGAATAAT | 64326 |
rs191042374 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176072083 | TGTTTTGAATTACCA[C/T]AGAAGTAGAAAACTC | 64326 |
rs191068085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176105209 | TAGCCGTTATTGATT[A/G]TAACTTTTTATACAG | 64326 |
rs191074333 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176164420 | TTCAGAGAGGTTAGA[G/T]TCCACCCCAACCCCA | 64326 |
rs191078570 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176196506 | GCAACACGGGTGTAA[G/T]GGAGAAACTCTTAAA | 64326 |
rs191079463 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176108672 | CTATCAGATGATTTC[G/T]TTGGTATCTAGTATT | 64326 |
rs191146369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175972241 | TCCCAAGTAACTAAT[A/G]ATTCTAAAGCAGGTG | 64326 |
rs191156555 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:175974569 | TAACAATGATTAATA[C/T]GGTTAAAGGGGTTGA | 64326 |
rs191207546 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175987293 | AAAGCTATACTTTAC[C/T]AATCTAAAGAAACAA | 64326 |
rs191218848 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175956977 | AATAAATAAATACAT[G/T]TAAAAATGGAAGAAA | 64326 |
rs191242251 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176185992 | GACTCAAATATGTAT[A/G]GATGATATTACAACA | 64326 |
rs191243106 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:175959951 | TTATCTTGTTTTGTG[C/T]TTCAGGTTTAACAAA | 64326 |
rs191244569 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176111089 | CCCGGGAGGCGGAGG[A/T]TGCAGTAAGCTGAGA | 64326 |
rs191246303 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176151152 | TACAATCGTCAAAAC[C/T]TCCAAAAAACATGTA | 64326 |
rs191250676 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176169674 | CAAGTCATAATCTTT[C/T]TGCTGGTAGAGAGTC | 64326 |
rs191259411 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RFWD2 | GRCh38.p7 | 1:176013632 | AATGTATTTCAACTC[A/G]CCATATAATATGTGA | 64326 |
rs191260071 | snp | G/T | 0.179425 | 0.239831 | intron-variant | RFWD2 | GRCh38.p7 | 1:175995462 | TGAATCCAGGAGCTG[G/T]TTTTTTGAAAGGATC | 64326 |
rs191260937 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176203953 | CAGCCTCCAATTCAG[A/G]TACGTCTTCTTGGGA | 64326 |
rs191266387 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176017667 | GTAGCTGGGACCACA[G/T]GCATGCGCCACCACA | 64326 |
rs191281692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176088562 | TTTTCTTTATATGTG[C/T]TTTACCTCCATTTCA | 64326 |
rs191290339 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176049464 | TGGGGGTAACAAGAT[A/C]CTTTTATACTGTAAA | 64326 |
rs191311594 | snp | G/T | 0.0451736 | 0.143339 | intron-variant | RFWD2 | GRCh38.p7 | 1:176168690 | CTTTCAGGATCAGGA[G/T]AGGGAAAGAGAGCAT | 64326 |
rs191341896 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176203850 | ACTGAAATTAGGTAC[G/T]TGACTATTTAAATCA | 64326 |
rs191364063 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176157700 | AGTTCAGGAATATAT[A/T]AAGGATTACAAAAAT | 64326 |
rs191391175 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175953053 | ATAACAGTGCTTTAA[A/G]GTGATTATAACACAA | 64326 |
rs191391783 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176164791 | CACTTTAAATTGGAT[A/C/T]TTTCTATTTTTCTAC | 64326 |
rs191409620 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176131570 | AGCCTGCTTAAAAGA[A/G]AGATCAAAACTTTTT | 64326 |
rs191413708 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176091300 | CTGAGATCGTGCCAC[C/T]GTGCCACTGTACTCA | 64326 |
rs191424235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176118489 | TAGAAGAGGCCAGGC[A/G]TGGTGGCTCATGCTT | 64326 |
rs191433379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176038471 | GGATGAAGGACTTAC[C/T]ACTTGATTTCAGACT | 64326 |
rs191441202 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176019805 | GGCAGAGGCTGCAGT[A/G]AGCCAAGACCACACC | 64326 |
rs191455682 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176005657 | TTCCATGAAGTTGAG[C/T]GGTTTTGAGTGAGAT | 64326 |
rs191459180 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176077845 | AACTTGGTAGCATTT[A/C]CATATACTAATAACA | 64326 |
rs191462229 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:175960543 | AGACTATTATGGAGG[C/G]TAAAAGAAGAGTTTA | 64326 |
rs191463200 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176096180 | ATTTTTGCTGCCCAA[A/C/T]GTGAGGCCAAAGGAA | 64326 |
rs191474569 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:175981616 | CTGAAAAATTTTTTG[A/G]CTAAAACTGCAAAAG | 64326 |
rs191477353 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176057012 | TATACCTCCAAAAAT[A/G]TTTATACTTCTCATC | 64326 |
rs191484144 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175980455 | AGAGAATAAAATTTA[A/T]TGATGTAACTGAAAA | 64326 |
rs191491873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176115105 | TAAAGGAATTCTTTT[C/T]AGTATTTTCGTAATT | 64326 |
rs191498255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176053883 | TTTTTTGTACTTTAC[C/T]TCCCTGGCAAAACTA | 64326 |
rs191560723 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176150534 | CCAAGCCTTCCACAT[G/T]GTTTGTGGGACTTCT | 64326 |
rs191568785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176185892 | CACTTAAAACTGTAA[C/T]TGAAAATACACTCAC | 64326 |
rs191570436 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176155566 | GAGCAAAGGGCTGAA[C/G/T]AAGTAATGGCTGACT | 64326 |
rs191570591 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176188894 | CAGAGTTGTGACATA[C/T]GTGAAATGTTCTAAC | 64326 |
rs191584856 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176175140 | ATTCACTCCCAACTC[A/G]GCAAGCATCACACCC | 64326 |
rs191595226 | snp | A/C/T | 8.66821e-05 | 0.0065829 | intron-variant | RFWD2 | GRCh38.p7 | 1:176081293 | CGACTGTCATCTATA[A/C/T]GAAAAAAAAAAAAAA | 64326 |
rs191595997 | snp | A/G | | | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176208807 | CTTTTGGCCAGGTGC[A/G]GTGGCTGAGGCCCAT | 64326 |
rs191602215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176191504 | CTTAATTTCTTAATT[C/T]TTCCTTTGCTTCCTT | 64326 |
rs191613333 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:176149878 | ATGAACAAACATCAT[C/T]CTAATTTTTTCTTAT | 64326 |
rs191623774 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176117559 | ACCAACCGTATAAAC[A/G]ATTATTTACTTTTTG | 64326 |
rs191632488 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | RFWD2 | GRCh38.p7 | 1:175944330 | CCGAAAATATATCCG[G/T]CCCTTTACAGAAAAA | 64326 |
rs191639696 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207323 | GGGGGATACAACTGG[A/G]GACGCAGCGGGGCTG | 64326 |
rs191654189 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176042106 | AGCAGAGCGAGATTA[C/T]GTCTCAAAAAAAAAA | 64326 |
rs191660830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176023757 | AAAGAAAAGAAAAGA[A/G]AAAGTAAACACATTG | 64326 |
rs191677374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175968194 | TAATATTTCCACATT[C/T]ATTCTACTTCCTGGT | 64326 |
rs191677401 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | RFWD2 | GRCh38.p7 | 1:176099707 | ATGCTTCCCTTTAAG[A/G]AGTCAAGCTCGACTT | 64326 |
rs191679001 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | RFWD2 | GRCh38.p7 | 1:176081826 | TAGAAAACTGCAATG[C/T]TATGAACTATTAATT | 64326 |
rs191680479 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175988956 | TTCTACTACTATACT[C/G]CAAGTAGATAAAATA | 64326 |
rs191683398 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176061947 | CTGACAAAGAACTTA[C/T]ATCCATAATATAAAA | 64326 |
rs191687999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176000949 | CAAAATTCTGCTGCA[A/G]TATAGCTCCATCTCC | 64326 |
rs191688213 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176016322 | ACTATAGATGGGAGA[C/G]GTGAAAAAAAACCAG | 64326 |
rs191706688 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175985983 | ATTTTAAAAATATGA[C/T]ACTAATAACTCATGT | 64326 |
rs191751781 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176013168 | CCAAAATTTATCTTA[A/T]TTTTTATTGTCATAT | 64326 |
rs191755353 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176009504 | TGTCCTTGTGTACTG[C/T]ACAAAAGTTTTACAG | 64326 |
rs191760152 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176036241 | GACATAAACTTCAAT[A/C]TTCAAAAAACTAGAA | 64326 |
rs191788323 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175972543 | GATCTCGGCTCACTG[C/T]AACTGCCACCTCCCG | 64326 |
rs191805012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176004739 | CTTTTTGATGTGCTG[C/T]GGGATTCGTTTTGCC | 64326 |
rs191814499 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176172391 | ACGAAAAAATTTTAA[C/T]GCAAACTTAAAAATA | 64326 |
rs191825891 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176160097 | TCAGAAAATAATAGG[A/G]AAGAATCTGTAATCT | 64326 |
rs191841263 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176179398 | AAAATAAATGATAGA[A/C]AATGTGCATATGACA | 64326 |
rs191843054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175948985 | CTGGCTAATATGGTG[C/T]AATCCTGTCTCTACT | 64326 |
rs191844559 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176103817 | TATAGGCAAAACCTA[G/T]AGTTAAAATCAGTAT | 64326 |
rs191847343 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176037584 | AACCTCAAGTCAAAT[C/T]TAGAAATACAGAAAA | 64326 |
rs191855289 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176065485 | GTTTTACATATAATG[A/G]CATCAGTTATTTGTA | 64326 |
rs191855641 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176194374 | GCTGGGCGCAGTGGC[C/T]CACACCTCTAATCCC | 64326 |
rs191859565 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176134815 | ACATTATAGTATTCT[A/G]CTCGCTAACTCTTCC | 64326 |
rs191879831 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176156975 | GGCCAAGGCAGGCAG[A/T]TCACCCAAGGCCAGG | 64326 |
rs191884734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176098546 | ATCTTCCAAAATAAA[C/T]TCTCTGTGTTAACAT | 64326 |
rs191891204 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | RFWD2 | GRCh38.p7 | 1:176060998 | AGGGACTTATACTAG[C/T]CAGTATAACTTTTGA | 64326 |
rs191899781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176136975 | CTGGTCTCCAACTTT[C/T]GAGCTCAAGCAATCT | 64326 |
rs191915604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176174447 | CCTAAGTTCCTTCTC[C/T]AAGTTTGCCATAAAA | 64326 |
rs191925420 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176130197 | AAAATGTTTTGCTTT[A/T]TTATTTAAATAAAGT | 64326 |
rs191934008 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176168531 | GGGAGGGAGGGGAAA[A/G]AAGCAAGCAAGCAAG | 64326 |
rs191991750 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | RFWD2 | GRCh38.p7 | 1:175964911 | AGAGCCTCTTGTCTT[A/G]TTTGGACAAAGGCAT | 64326 |
rs192013198 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | RFWD2 | GRCh38.p7 | 1:175993093 | CGGTTCACGAAAAGC[C/T]GCTGTTCTGCAGCCA | 64326 |
rs192042186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175953647 | AGATAAGATACACCA[C/T]GCAAACATTAATCGT | 64326 |
rs192043102 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176031541 | TAAAAGAAAATATCA[G/T]CTTCTAGGTGAAGAG | 64326 |
rs192044820 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176068458 | AGATGATTATGAGGC[A/G]CTGTCCTAAAAACAG | 64326 |
rs192048636 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176172218 | ACACGCCTGGCTAAT[A/T]TTTTATAGAGACAAG | 64326 |
rs192049495 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176046934 | TACACATTCCTCATA[A/T]CACAAAAGAGGTTAA | 64326 |
rs192062214 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175998324 | TGTGGGGTGGGGGGA[C/G]AGGGGAGGGATAGCT | 64326 |
rs192071694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176105743 | GGGAGTTGTTTTGGC[A/G]CAAAACACATCAGTT | 64326 |
rs192078499 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176123224 | AAGAAGCATTCCAAA[A/C]ACAATTAATTAAAAA | 64326 |
rs192086914 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175973161 | TAACACTTTTACAAG[G/T]CTAATTTTTAGTGAA | 64326 |
rs192091940 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | RFWD2 | GRCh38.p7 | 1:176087088 | TGGATCCCTTCCTTA[C/T]ACCTTATACAAAAAT | 64326 |
rs192096920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176024608 | CCACTTCTATTTAAC[A/G]TTGTACTTGATCTTC | 64326 |
rs192097500 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:175991664 | ACATACATTGTACAG[C/G]TGGACAAAAGTATTT | 64326 |
rs192098461 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:175991733 | GGAAAAAGCTTTTTA[A/T]ACTTTTTTGTTAAAA | 64326 |
rs192100557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176019689 | AACATAGTGAAAATA[C/T]GTTTTTCCAAAAAAT | 64326 |
rs192105401 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | RFWD2 | GRCh38.p7 | 1:176005094 | GGGAGGGTGTATGTG[A/T]CGAGGAATTTATCCT | 64326 |
rs192105783 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:176008007 | GGAGACTCCGTGGGC[A/G]TAGGACCCTCGGAGC | 64326 |
rs192122553 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176109066 | GCAGTGAGCTGAGAT[C/G]ACGTCACTGCACTCC | 64326 |
rs192123490 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175948256 | GGAAGAATGGAGACA[A/T]GCCTCCTGTAGGAAA | 64326 |
rs192126324 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:175994216 | ATCTGTCACCACCAG[A/G]CCTGCCCTAAAAGAG | 64326 |
rs192132475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176063704 | TAAGTTGCCTAAACA[C/T]AGGTTAGCTTTTGTC | 64326 |
rs192140730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176073646 | ACCATCTTCTACTTA[C/T]GAGAGTGAACTTCAC | 64326 |
rs192141915 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:176085192 | CTCGAATAGCCCATA[A/T]ACAACTCCTCTGAAA | 64326 |
rs192142586 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176090124 | TAATCTCAGGTCTTT[A/G]GATAGTAACTTAACT | 64326 |
rs192153342 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176159491 | TTAAAATGTGCACAC[A/C]TACCCTAATGCGAGC | 64326 |
rs192157875 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176126266 | CTACGTTGAGTAACA[C/T]TGGTGAAAGTGGGCA | 64326 |
rs192158562 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176019152 | GCTTGGGCAACAGAG[C/T]GAGAATAGACTTTTT | 64326 |
rs192160595 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176125068 | GTTTGTCTTGAGAAA[A/T]GTCTAATCTTTTACC | 64326 |
rs192171132 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | RFWD2 | GRCh38.p7 | 1:176154441 | GGTGTACATACACGA[C/T]AGAATGCTATGCAGC | 64326 |
rs192171389 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176141450 | AGGTTGCAGTGAGGC[A/G]AGATAGTGCCACTGC | 64326 |
rs192174653 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176160351 | ATATCATTCAGGACA[C/T]AGGAATGGGCAAAGA | 64326 |
rs192175166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176121639 | ATAAATGCAGTTCTC[C/T]TCTAGGACAGTATTT | 64326 |
rs192176224 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176194557 | GCAGGAGAATCACTC[A/G]AACCCAAGAGGAGGA | 64326 |
rs192180138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176179013 | AAAAAAGACAAGGCC[A/G]GGTGCAGCGGCTCAC | 64326 |
rs192247988 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176024304 | ATCCATTACTAACAC[A/C]GACACAAAAGTACTT | 64326 |
rs192271786 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:175978599 | GCACTGAGGAGGAGA[A/T]GGGAGTCTTTCTGGA | 64326 |
rs192281507 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176062735 | AACTAAAACCCAGAC[A/C]AGTTTATTCAAATAA | 64326 |
rs192304728 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176100475 | AAATTCTACATTCCT[G/T]TGTTATTTTTAAGTG | 64326 |
rs192310362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175961358 | TCGTTTCATTATACA[A/G]TAGTGACTTTGGCAT | 64326 |
rs192321596 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:175982212 | GAGTTAAAATTAGGT[C/T]ACAGAAAAAAACATG | 64326 |
rs192343791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176045432 | CAAACATACTATGTA[C/T]GCCATTCATTAAAGA | 64326 |
rs192347126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175975384 | ACCCACAACCATCCC[A/G]AAGTTATTACTCTTG | 64326 |
rs192354551 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176010515 | GCACATTGTTCCACA[A/C]ATCTGAATTTGTCTA | 64326 |
rs192377305 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176006561 | GGTGACAAAATCCCT[C/G]AGCATTTGCTGGTCT | 64326 |
rs192379874 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176147702 | AATATAAAAACACTA[C/G/T]GCCAAAGCTATAAAA | 64326 |
rs192380428 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175996181 | ATGCAGAAAAGGCCT[C/T]TGACAAAATTCAACA | 64326 |
rs192382693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176067837 | GCCCACTGGGGCTTC[A/G]GGAGCTGTAAACGTT | 64326 |
rs192390706 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176046391 | TTTCTAAAGTAATTC[C/G]GTCTACAAGGATAAA | 64326 |
rs192394577 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176028760 | CTTTTTATTATTATT[A/T]TTATTTTTGAGACAG | 64326 |
rs192420166 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176183447 | TCAAAAACCAACAAC[A/G]GAAAATAAGAGTTGG | 64326 |
rs192444063 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176204561 | AAATCAGATTCTCAT[A/T]AATTAATTCTTCTGA | 64326 |
rs192476098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175950919 | ATAGTTTTATCTTTA[C/T]TGACTTGCTTAAAAA | 64326 |
rs192494407 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175991957 | CTTAAAAAAACAAGT[G/T]TAAGAAGTACAGTCT | 64326 |
rs192510591 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176010035 | TTTTAGCTTTGAAAA[A/C]AATATCCAGTCTGCA | 64326 |
rs192524850 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176143260 | CAATAAATTTGAAAA[C/T]TGAGATGACATAAAC | 64326 |
rs192539633 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175976869 | TGAGGACTTTTTTTG[A/C]AAGTTGTAACAAGTC | 64326 |
rs192567915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175966963 | TTGAGATCTGGGGAA[C/T]TGGGATTTCTTCATC | 64326 |
rs192573906 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176180237 | CAAACTCAGTAAATG[C/T]TGAATGCATGAATGA | 64326 |
rs192606959 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RFWD2 | GRCh38.p7 | 1:176034785 | CCCAAGTCCTAAACT[A/G]AGCTCTAACTGGCAT | 64326 |
rs192620156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176128675 | CTTCAAGGTTTGAGA[A/G]AAAGTATTAAATTGT | 64326 |
rs192628677 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176096701 | TAGAAAATGTTTTAC[A/G]AGGCCAAGACCCCAA | 64326 |
rs192630198 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176115575 | AACATGGTGAAACCC[C/T]GTTTCTACTAAAACT | 64326 |
rs192635816 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176166023 | AATTTTACCACAAAA[C/T]CTTATATACCATTAT | 64326 |
rs192661461 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | RFWD2 | GRCh38.p7 | 1:176148393 | AGCCAGTTAGAAATT[A/T]AAAAAAAAAAAAAAA | 64326 |
rs192664439 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | RFWD2 | GRCh38.p7 | 1:176184153 | TTTAAAATTAAAAAA[A/T]TTTTTTGATGTATGA | 64326 |
rs192670963 | snp | A/C/G | 0.00874735 | 0.0655527 | intron-variant | RFWD2 | GRCh38.p7 | 1:175977661 | GACTGTACAAGTAAA[A/C/G]TACAAAAAAAAGTTT | 64326 |
rs192676962 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176082218 | ACTTTAGTTTCCTAG[A/C]CTGAAACTGAGACAA | 64326 |
rs192680617 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176199204 | CGCCTGTAATCCTAG[C/G]TACTCGGGAGGTTAA | 64326 |
rs192697252 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176042327 | GCACTTTCAGAGGCC[A/G]AGGCAGCAGGGCAGA | 64326 |
rs192741748 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176128326 | ATTTTAATGAGAAAT[C/T]ACAGGTGTATGAAGA | 64326 |
rs192754073 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176137482 | CTAACGCCAGGATGC[C/G]GTTGTCTTACTCTAA | 64326 |
rs192756117 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176165014 | ATAGACCCAACTGTC[C/T]GATACTTCCCAGTAT | 64326 |
rs192758402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176109429 | CCTTTATCACAGACT[A/G]TTAATTACTTTTTGG | 64326 |
rs192760234 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RFWD2 | GRCh38.p7 | 1:176199124 | GGATCGAGACCAACC[C/T]GGCCAACACAGTGAA | 64326 |
rs192766622 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176074268 | TAATTAAATTTCCTT[C/T]TTTGGGAGGAATTAG | 64326 |
rs192767863 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176142494 | AAAGATAATGAGACA[G/T]TAATAGGTATAACAA | 64326 |
rs192795826 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175973582 | AGATAACTTTGTAAG[A/C]CTTAAGAGTTTTTGA | 64326 |
rs192803811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176205293 | ATTTATAAATAACAA[C/T]CATATTACAGCCCAA | 64326 |
rs192805021 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176028006 | CATGTCTTACCTGGG[G/T]GCAGGCAAGAGAGCG | 64326 |
rs192815114 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175956579 | CTAAATCTTTTTCTT[A/T]AAGTGACAATATCAA | 64326 |
rs192816852 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176190870 | TCAACTGTCTTATAG[C/T]AGTACTGGTTCCAAC | 64326 |
rs192824669 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:175993645 | AAGAAAGGGTATCAG[C/T]GATGGAAGATGAAAT | 64326 |
rs192851650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176051665 | TCATAGGAGATGACA[A/G]CTCCATGTGTGTTAC | 64326 |
rs192860537 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | RFWD2 | GRCh38.p7 | 1:175996277 | CTATCTATGACCAAC[A/C]CGCAGCCAATATCAT | 64326 |
rs192867709 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176055436 | GTGAAACTCCATCTC[A/C]AAAAATAAACAAAAC | 64326 |
rs192877783 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175962529 | AAAAACCTCCAAACC[A/G]AGCCTTTTCATTGGG | 64326 |
rs192879617 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176095505 | CGCAGCATGGCAAAA[A/C]CCTGTTTCTATAAAA | 64326 |
rs192888781 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176029487 | AAAATAGATTTTCAG[A/T]ATATAAGTTGTCATC | 64326 |
rs192899822 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176127839 | TCTTCCAATGTAGCT[C/G]TACTATTTACAATAC | 64326 |
rs192909153 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:176051109 | AATTAGTAGAAGAGA[C/T]TACAGACAATATATG | 64326 |
rs192918522 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176082973 | AGTTGTGCTTCCATT[C/G]TAAAGACAGCAAAAG | 64326 |
rs192928816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176119300 | GTGTAGTTGCATATT[C/T]AGAGGCCTATAGAAC | 64326 |
rs192951490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176152954 | AAAACTTCTAAAGGA[C/T]ATTCACTTCTGCTTG | 64326 |
rs192964190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176090644 | ATTAAGCCCAGGGAC[C/T]GCAAGTAGGGAAACT | 64326 |
rs192981722 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175987852 | CAACAATAAAAGCCA[C/T]AGAATAACAGATCAA | 64326 |
rs192985335 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:176125847 | AATATTGATTCTTCC[A/G]ATCATTAACATGGCA | 64326 |
rs192990312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176015735 | AGAAATAGAGGAGTG[A/G]TCAATTATATTAAAT | 64326 |
rs193034190 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176208372 | AGGCTGACATGGGAG[A/G]ATTGCTTGAGCTGGG | 64326 |
rs193058526 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176186086 | AGCTACAAAGGGACC[A/C]ATAGTAAAGAAAACT | 64326 |
rs193062354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175983032 | GAGAATAAGATTTTA[A/G]ATGTTCCCACTACAA | 64326 |
rs193073325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176011115 | TCTCAAAGTTTTTGT[C/T]GGTGTGAAAAACAAA | 64326 |
rs193078352 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176038265 | CCCTACATATGGAGA[C/G]ATAAACCATGTTCAT | 64326 |
rs193093312 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176077600 | TTAAAACAAGACAAG[A/G]ATGCCCACTTTCACC | 64326 |
rs193127558 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176078960 | CATCTCATAGCAGAA[A/T]GGCAATTATTAAAAA | 64326 |
rs193129983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176105353 | AAGAAATATCACAAC[A/G]AAAATTGAAGAAAAT | 64326 |
rs193130830 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176038946 | AGCAATGAAACAGCT[A/G]AACTGAATGGTACCA | 64326 |
rs193132528 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176147276 | TGTCTGCACTAAAAC[A/G]TATTTTCTAGACTAA | 64326 |
rs193135951 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176173467 | ATAGTGAGACCTTGT[C/T]TCTACAAAAACAAAC | 64326 |
rs193136331 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176136258 | TTTGTCAGTCTAATC[A/G]AGAAAAATTATGGCA | 64326 |
rs193143762 | snp | C/T | 0.00279162 | 0.0372561 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176208150 | AATATTGAAAATTGA[C/T]TATAGGCGGGCGCGG | 64326 |
rs193152654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176114447 | AGAAGTGATATAATC[C/T]AAAAGGATTTATTGT | 64326 |
rs193172665 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176101153 | ACCCTGTAGCATGCC[C/T]CCCACCATCAACATC | 64326 |
rs193174035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176194074 | ATGAAATATTTGAAG[A/G]TAGAACACAAAAAGT | 64326 |
rs193177094 | snp | C/T | 0.0175006 | 0.0918915 | intron-variant | RFWD2 | GRCh38.p7 | 1:176132520 | ATGTGTGTGTGTATA[C/T]ACACACACACATATA | 64326 |
rs193178042 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176170489 | TGTATCAGAGCTCTT[G/T]GGTGACCAGGTGCAT | 64326 |
rs193195867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176000694 | GAAAAAGGGTTCTCA[A/G]CCTGTATATGGTAGA | 64326 |
rs193203050 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant, utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175967521 | AACAAACAAACAAAC[A/C]AACCCAGCTGTGGCT | 64326 |
rs193280788 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176122739 | ATGTTTATTACATAA[C/T]AATTCTGAAACTGAA | 64326 |
rs193281655 | snp | C/G | 0.179744 | 0.239925 | intron-variant | RFWD2 | GRCh38.p7 | 1:176057850 | AGTCTGGGAAGTAAG[C/G]AGCGCCTCTTCCCCG | 64326 |
rs193282291 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176086686 | ATGGCCATACTGCCC[A/G]AAGTAATTTATAAAT | 64326 |
rs193290375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176156434 | GGTGTAGACTCAAAC[C/T]GAACTATATCAATAA | 64326 |
rs193292276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176190281 | TTTCTTTGCGTGTCA[C/T]GGTGGCACTCAAAAA | 64326 |
rs199511428 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176151355 | AAGGAAAGAAAGAAA[A/G]AGAAAGAAAGAAAGA | 64326 |
rs199512898 | snp | C/G | 0.00199792 | 0.0315431 | intron-variant | RFWD2 | GRCh38.p7 | 1:175947164 | TAAAAATGGGCCTGA[C/G]TTTAAAATGGAGATA | 64326 |
rs199518398 | in-del | -/CAG | 0.00210263 | 0.0323558 | intron-variant, nc-transcript-variant, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175968526 | CCACATGGCTGGTTC[-/CAG]CAGCAGCTTCCATTT | 64326 |
rs199534494 | in-del | -/GT | | | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176208571 | TTATTTGGGAATAAA[-/GT]GTGTGAAAATACTCA | 64326 |
rs199541144 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176143151 | GAGCGAGAGAAAGAG[A/C]GAGAGAGAGAGAGGA | 64326 |
rs199549348 | in-del | -/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176084856 | ATACCAGACTTTTTT[-/C]TTTTCCCCCTTGGTG | 64326 |
rs199557106 | snp | A/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176208463 | TCTCAAAAAAAAAAA[A/T]TTTTTTCATTTGCCG | 64326 |
rs199576832 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-5-prime, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207094 | GCCCGCCGAGCCGGA[C/T]GTGGGGCTGAGGAAC | 64326 |
rs199577703 | snp | C/G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176016989 | AATATTACAGAATAA[C/G/T]TTCTAGTACAACAAA | 64326 |
rs199590653 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175998492 | AAAGAGAAAAAAAAG[-/A]AAAAAAAAATAGAAC | 64326 |
rs199602863 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175959390 | CCCTTTGGTGAGGAA[A/C]AAGTCAACGATGCCA | 64326 |
rs199616588 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176072889 | ATTTTGACCTCCTTA[C/T]AGGAATAGGGATACA | 64326 |
rs199623331 | in-del | -/GTGTGT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176187403 | CACATATAAATATAC[-/GTGTGT]GTGTGTGTGTGTGTG | 64326 |
rs199624244 | in-del | -/TATA | 0.0158469 | 0.0875917 | intron-variant | RFWD2 | GRCh38.p7 | 1:176133269 | ACGTATATACGTACG[-/TATA]TATATACGTATGTAC | 64326 |
rs199626894 | snp | G/T | 1.66101e-05 | 0.0028818 | missense | RFWD2 | GRCh38.p7 | 1:176085791 | CTGAGATACGAGACA[G/T]CCTTGTAGAAAAGTA | 64326 |
rs199626941 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176094021 | GTGAGACTCTGTCTC[-/A]AAAAAAAAAAGGAAA | 64326 |
rs199679719 | in-del | -/GTGT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176165362 | AGAGAGATGTGTGTC[-/GTGT]GTGTGTGTGTGTGTG | 64326 |
rs199702008 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176078618 | CTTCAAAAGCAATTG[A/C]AAAAAAAAAAACAAA | 64326 |
rs199724444 | in-del | -/TAAA | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176105016 | TTCCTCATAAATTGT[-/TAAA]TAAAGTACAGAAAAA | 64326 |
rs199725452 | in-del | -/TTTA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176002347 | CTTTCTTTTTTAGTT[-/TTTA]TTTATTTATTTATTT | 64326 |
rs199730279 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176130414 | ATAAAATGTAAACTA[C/T]GGTTTATACTGAGAA | 64326 |
rs199734681 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176032243 | AGAGTGCTATTTCAA[G/T]AAAAACTACCATAAA | 64326 |
rs199737653 | in-del | -/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176141730 | TTCATAGCACTTTTT[-/C]TTTTCTTTTTTTTTT | 64326 |
rs199739617 | snp | A/C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176157860 | GCAATAGAAACTATC[A/C/T]AAAATGCACTAGAAA | 64326 |
rs199744717 | in-del | -/AACT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175953951 | ATAAAAACCAAACTG[-/AACT]AACTGACATTTACAG | 64326 |
rs199751706 | in-del | -/GAC | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176126463 | CACTTCTTTTTTCTT[-/GAC]TTCTTTTTTTTTGAG | 64326 |
rs199758339 | in-del | -/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176127567 | AGTATTCTACTGTGT[-/G]TGTGTGTGTGTGTGT | 64326 |
rs199768963 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176119643 | CATTATACATTCATA[C/T]ACACACACACACACA | 64326 |
rs199770317 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176063125 | ACTGCAGTGGCGCAA[C/T]CTCGGCTCACTGCAA | 64326 |
rs199785652 | in-del | -/AAAAAAA/AAAAAAAA | 0.102726 | 0.202016 | intron-variant | RFWD2 | GRCh38.p7 | 1:176035711 | CAATAAAACGAGACC[-/AAAAAAA/AAAAAAAA]AAAAAAAAAAAAAAC | 64326 |
rs199793579 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175949168 | AGCAAGGCTCCGTCT[A/C]AAAAAAAAAAAAAAA | 64326 |
rs199823550 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176146309 | TAACTAACAAACGCT[A/G]TTAATAGGCAAGTTC | 64326 |
rs199826928 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176133224 | CACACATACGTATAT[A/G]CGTACGTATATGTAC | 64326 |
rs199833741 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175965046 | ACCTGCCTTAAGCTC[C/T]TTTTCATACCAAGAT | 64326 |
rs199850457 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175983144 | TGTACCCCATAAATA[A/C]TTACAATTATTATTT | 64326 |
rs199859842 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176147985 | GCTCACCACAAGCTC[C/T]GTAACAGGCAACTTT | 64326 |
rs199868483 | snp | C/T | 1.65957e-05 | 0.00288055 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176176012 | TACACTTGTAGCTAT[C/T]AGTAGGGGGGGAAAA | 64326 |
rs199875514 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176048344 | GTGCCCAGCCAATTT[-/A]AAAAAAAAAATTTAT | 64326 |
rs199889061 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176039581 | AAGAATGTTTTACAG[A/G]AAAAAAAAAAATTAC | 64326 |
rs199893490 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175998259 | AGGTGGGAATTGAAC[A/G]ATGAGAACACATGGA | 64326 |
rs199899061 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175952253 | ATGGTGAAACCCCAT[C/G]TCTACTAAAAATACA | 64326 |
rs199915441 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175958375 | TCTCTGTAACCATTC[-/A]GGTATAATATCAAAG | 64326 |
rs199939407 | snp | A/T | 0.00306446 | 0.0390236 | intron-variant, nc-transcript-variant, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175968482 | GTAGGATCGCTGCAA[A/T]CTGTAGACAAAAGGC | 64326 |
rs199947817 | in-del | -/GT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176127590 | TGTGTGTGTGTGTGT[-/GT]ATGTGTATATATGTG | 64326 |
rs199970155 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176135939 | GCAAAAAAAAATTAC[A/C]ATACATATAAATAAC | 64326 |
rs199988146 | in-del | -/AATAAA | 0.093777 | 0.195178 | intron-variant | RFWD2 | GRCh38.p7 | 1:176026346 | ATACATAATATTAAT[-/AATAAA]AATAACAACTATAAG | 64326 |
rs200005801 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176199397 | TTAAAACTAAACATA[C/T]ACTTGGCAGAGAACT | 64326 |
rs200038208 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176121511 | CATTTCTTTAAATGT[C/T]GTTTTTTATTTTTAT | 64326 |
rs200062225 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176190582 | AGAAAATTATTTCAC[A/G]TATCTAATATGCATT | 64326 |
rs200064428 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176081344 | AACTGCAAAGTAAGT[G/T]AAAGAGCCACATCCA | 64326 |
rs200066182 | in-del | -/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176117917 | AAACAAACAAACAAA[-/C]AAAAAACCAACAAAA | 64326 |
rs200091101 | in-del | -/AAAC | 0.180383 | 0.240111 | intron-variant | RFWD2 | GRCh38.p7 | 1:176117898 | AGACTCTGTCTCGAA[-/AAAC]AAACAAACAAACAAA | 64326 |
rs200091789 | snp | C/T | 0.00199806 | 0.0315443 | intron-variant | RFWD2 | GRCh38.p7 | 1:175988453 | ACTTACTTAAAATTT[C/T]TTGGCACGAAACTCA | 64326 |
rs200092076 | in-del | -/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176091183 | AATGAAGTTTATTAC[-/G]CAGTGAGCCATCTCT | 64326 |
rs200116976 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175953760 | TTAAATAAGGGTCAA[A/C]TTATAAAAAAAAAAA | 64326 |
rs200127542 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175996279 | ATCTATGACCAACCC[C/G]CAGCCAATATCATAC | 64326 |
rs200141050 | in-del | -/AC | 0.0142736 | 0.0832652 | intron-variant | RFWD2 | GRCh38.p7 | 1:176139124 | TGGGCACAGACATAA[-/AC]AGACAATTCCCAAAA | 64326 |
rs200159764 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176113961 | TTTTTTTTTTTTTTT[A/T]TAGTTTGCACAGTGA | 64326 |
rs200162912 | in-del | -/AC | 0.0205511 | 0.0992634 | intron-variant | RFWD2 | GRCh38.p7 | 1:176073960 | GCCTCTTTGTTTGAG[-/AC]AGAGTCTCATTCTGT | 64326 |
rs200184537 | in-del | -/A | 0.0448719 | 0.142907 | intron-variant | RFWD2 | GRCh38.p7 | 1:175996131 | CCAGCATATAAACAG[-/A]ACCAAAGACAAAATC | 64326 |
rs200187869 | in-del | -/AAAGAAAGAAAGAAAGAAAGAAAGAAAG | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176151354 | GAAGGAAAGAAAGAA[-/AAAGAAAGAAAGAAAGAAAGAAAGAAAG]AAAGAAAGAAAGAAA | 64326 |
rs200189247 | snp | A/C | 3.62122e-05 | 0.00425497 | intron-variant | RFWD2 | GRCh38.p7 | 1:176135106 | AAATAAAATTATTTG[A/C]ATTATAGTAGATATT | 64326 |
rs200195810 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176173318 | TTTGTCTCAAAAAAA[A/C]AAAATGAAAAAAAAA | 64326 |
rs200218769 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176025895 | AAAAACAAAAAAACC[-/A]AAAAAAAAAGAAAAC | 64326 |
rs200235905 | in-del | -/ATATAA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175951458 | TATATATATATATAT[-/ATATAA]AAACTTCCATTTTTG | 64326 |
rs200274554 | snp | C/T | 6.59152e-05 | 0.00574049 | synonymous-codon | RFWD2 | GRCh38.p7 | 1:176081214 | TGTGGCTAAAGGTCG[C/T]ACTGAATTATATCGA | 64326 |
rs200304738 | in-del | -/AT | 0.0581099 | 0.160244 | intron-variant | RFWD2 | GRCh38.p7 | 1:175954929 | TTTCAACATTAAAAA[-/AT]ATATATATATATAAT | 64326 |
rs200323555 | snp | C/T | | | synonymous-codon | RFWD2 | GRCh38.p7 | 1:175989409 | TGCATAAGAGACTGC[C/T]TTACGGTGTCCTTTG | 64326 |
rs200324839 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176188446 | AAAAACGTATCCATT[C/T]AGAACCATCCATTTA | 64326 |
rs200326765 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176151357 | GGAAAGAAAGAAAAA[A/G]AAAGAAAGAAAGAAA | 64326 |
rs200356934 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:175953047 | AAAATAATAACAGTG[C/T]TTTAAGGTGATTATA | 64326 |
rs200366580 | in-del | -/A | 0.106968 | 0.205041 | intron-variant | RFWD2 | GRCh38.p7 | 1:176035265 | AACTATTTTTTTTTT[-/A]AAAAAGAATCAAATG | 64326 |
rs200376988 | in-del | -/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176169544 | ATATACATAAAAGTT[-/C]TGTTTACGCTATACC | 64326 |
rs200380289 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176101247 | AGGACAGAGGAAAGA[A/G]AGAGGAACACCTCAC | 64326 |
rs200383519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176202723 | AAGAATGGTCAACAG[A/G]CTTCATTTTTAGTGC | 64326 |
rs200394860 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175957104 | AATTATAAAGTAAAA[A/T]GTTACAGTAAACTAT | 64326 |
rs200403081 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176068665 | ACATGAAACCTTGAA[G/T]GAATGAACTTTATTC | 64326 |
rs200414002 | in-del | -/A | 0.255503 | 0.249939 | intron-variant | RFWD2 | GRCh38.p7 | 1:176095681 | AAGACCCTGTCTCAG[-/A]AAAAAAAAAAAAAAA | 64326 |
rs200419927 | in-del | -/AGT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176089296 | GACTCTGTCTAAAAC[-/AGT]AATAACAACAACAAC | 64326 |
rs200423124 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176058773 | AAAAAAAAAAAAAAA[C/T]AATGTGACCTCTTAT | 64326 |
rs200429629 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175977038 | ACAAAGATATGTTTG[G/T]TGAGTCATGGCATTA | 64326 |
rs200452101 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175993190 | CTGAGGGTCCTGTCT[G/T]TTAGAAGGAAAACTA | 64326 |
rs200465038 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176079647 | TAATTAAAAAAAAAA[-/A]GGTTCAAGGTATTAA | 64326 |
rs200472979 | in-del | -/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:175962973 | ATCGTCAAATAAACA[-/T]TTTTTTTTAATATGT | 64326 |
rs200491746 | in-del | -/GCC | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176033383 | GTGAGCTGAGATCGT[-/GCC]GCCATTGCACTCCAG | 64326 |
rs200501279 | in-del | -/GGG | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176009878 | AAGTTTAGGTTACTT[-/GGG]GGGGGGGGGTCCGCA | 64326 |
rs200510116 | in-del | -/A | 0.0441095 | 0.141807 | intron-variant | RFWD2 | GRCh38.p7 | 1:176167653 | AACATTTCTTAGTAC[-/A]AAAAAAAAATGCATT | 64326 |
rs200528462 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176140231 | ACATAAGGTGAACCT[A/C]ATAAAACTGCCAATA | 64326 |
rs200563057 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176139288 | CAAAAACAAAAAAAA[A/C]AAAAAAAAAAAACAA | 64326 |
rs200568162 | in-del | -/ATAA | 0.0189856 | 0.0955633 | intron-variant | RFWD2 | GRCh38.p7 | 1:176109989 | AGAAATTTTTGATAA[-/ATAA]TGTTTCCACTAGCGG | 64326 |
rs200588441 | in-del | -/TTGT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176073951 | CTTGTTTAGGCCTCT[-/TTGT]TTGAGACAGAGTCTC | 64326 |
rs200602904 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175958376 | CTCTGTAACCATTCA[A/G]GTATAATATCAAAGC | 64326 |
rs200644304 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176139300 | AACAAAAAAAAAAAA[-/A]CAAAAAAAGAGATGC | 64326 |
rs200656420 | in-del | -/AAC | 0.00914312 | 0.0669923 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176208671 | TGAGAATTACATAAT[-/AAC]TGTTTTTAAACCGTT | 64326 |
rs200684887 | in-del | -/TTTG | 0.108755 | 0.206276 | intron-variant | RFWD2 | GRCh38.p7 | 1:176106038 | TGTTTTTTGTTTTGT[-/TTTG]TTTTTTTGAGACAGA | 64326 |
rs200689713 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175949765 | ATTTAAAGCCGAAAG[C/T]TCCATCTCCTTCTGC | 64326 |
rs200692518 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175995329 | CCTAACATCACAATT[A/T]AAAGAACTAGAAAAG | 64326 |
rs200750059 | snp | A/G | 0.00130463 | 0.0255071 | missense, utr-variant-5-prime, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176206857 | GCTGCCGCCGAAACC[A/G]CCACGGAAGGCGGCG | 64326 |
rs200753525 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176202676 | TGTCTCAAAAAAAGG[-/A]AAAAAAAAAATTGGA | 64326 |
rs200754825 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176099140 | ACCCTGGACATTTTG[G/T]TATTCACAGACAATT | 64326 |
rs200758746 | snp | C/T | 0.000267715 | 0.0115666 | intron-variant | RFWD2 | GRCh38.p7 | 1:176046151 | TTGTTACATCTATAC[C/T]GCATCATGTCAAGAA | 64326 |
rs200772272 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176037394 | CCTGGGCGACAGAGC[A/G]AGACTCCGTCTCAAA | 64326 |
rs200781209 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176121516 | CTTTAAATGTCGTTT[G/T]TTATTTTTATGTTTT | 64326 |
rs200782313 | in-del | -/AA | 0.0166325 | 0.0896639 | intron-variant | RFWD2 | GRCh38.p7 | 1:175957061 | GCTAAAAGTTATTAC[-/AA]AAGAGTCAAAAAGTG | 64326 |
rs200797485 | in-del | -/TC | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175986552 | TGTACCAATTCTTTT[-/TC]TCCCTCCCTATTAAA | 64326 |
rs200799929 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176119663 | ACACACACACACACA[C/T]ATATAGAAAAGAATA | 64326 |
rs200811678 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176011936 | ACAATATATGATAAA[A/C]AACTGTGTTACTGGC | 64326 |
rs200814695 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | RFWD2 | GRCh38.p7 | 1:176133226 | CACATACGTATATAC[A/G]TACGTATATGTACGT | 64326 |
rs200821265 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176112207 | CATAAAAGTAAGTGC[G/T]ACTCTAAAATATTTC | 64326 |
rs200826998 | snp | C/T | 0.00199792 | 0.0315431 | intron-variant, downstream-variant-500B, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175968362 | TACTGAATAAAATGG[C/T]AAGGAAACCAAGTAT | 64326 |
rs200830965 | in-del | -/TGTGTA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176127586 | GTGTGTGTGTGTGTG[-/TGTGTA]TGTGTATATATGTGT | 64326 |
rs200858337 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176141735 | AGCACTTTTTCTTTT[C/T]TTTTTTTTTTTTTAA | 64326 |
rs200876520 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176087048 | TTCTGGGAAAACTGG[C/T]TAGCCATATGTAGAA | 64326 |
rs200877780 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176202338 | GGGACTACAGGCACA[A/G]GCCACCACACAGGCT | 64326 |
rs200903696 | snp | C/T | 0.00199792 | 0.0315431 | intron-variant, nc-transcript-variant, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175968509 | AGGCATTTTTTCATT[C/T]GTCCACATGGCTGGT | 64326 |
rs200911615 | in-del | -/T | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176176888 | CAATCTCAACTACTG[-/T]TACAGAAAATGTTAA | 64326 |
rs200911979 | in-del | -/GAG | 0.430732 | 0.172731 | intron-variant | RFWD2 | GRCh38.p7 | 1:176005751 | TCTTTTACATTTGCT[-/GAG]GAGAGCTTTACTTCC | 64326 |
rs200919116 | in-del | -/T | 0.030665 | 0.119967 | intron-variant | RFWD2 | GRCh38.p7 | 1:176097558 | TCTATAAAAAAGCTC[-/T]TTTTTTTATAGAGCT | 64326 |
rs200929415 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176178447 | AGTGGGCAGAGATTG[A/C]ATCACTACACTCCAG | 64326 |
rs200952729 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175951882 | AAAATATATGAAAAC[C/G]TTAAGACTAAAATGT | 64326 |
rs200968143 | in-del | -/G | 0.0217236 | 0.101931 | intron-variant | RFWD2 | GRCh38.p7 | 1:176071310 | GATGAGGCCTCCCTA[-/G]AAACTGAGCAGATGC | 64326 |
rs201017348 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175983145 | GTACCCCATAAATAC[A/T]TACAATTATTATTTG | 64326 |
rs201035364 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175976073 | GAATTAGAAGGTCTC[A/G]AAGGTCTCAATCCTT | 64326 |
rs201048105 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176095136 | GCATGGAAAACTATC[A/G]TTATTTACACAATAA | 64326 |
rs201051472 | snp | A/C | 0.00199792 | 0.0315431 | missense | RFWD2 | GRCh38.p7 | 1:176085879 | GCTATTATACCAAGG[A/C]TGTTTCTTTGTCTAA | 64326 |
rs201071402 | snp | A/G | | | missense | RFWD2 | GRCh38.p7 | 1:175989402 | CAAACTTTGCATAAG[A/G]GACTGCTTTACGGTG | 64326 |
rs201075229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176106967 | GATTCTAAATCTGGT[A/G]ACAAAGCAATTCCGG | 64326 |
rs201078047 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176076549 | AATTAATGACCTTAC[A/C]TCACATGTAGAGGAA | 64326 |
rs201097782 | snp | C/T | 0.000167701 | 0.00915545 | intron-variant | RFWD2 | GRCh38.p7 | 1:176148982 | GTAAATAAAACATTA[C/T]GTAAAACACACAAAA | 64326 |
rs201133714 | snp | G/T | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176185615 | TAGTAAGGAAGAAAA[G/T]GGAAGGATAAAAGGA | 64326 |
rs201138357 | in-del | -/C | 0.0333695 | 0.124785 | intron-variant | RFWD2 | GRCh38.p7 | 1:176086651 | ATGCTCATGGATAGG[-/C]AAGAATCAATATTGT | 64326 |
rs201150541 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176190530 | TCACTTGGGACATTT[A/T]AAAAAAAAAAAAACA | 64326 |
rs201204985 | snp | C/T | 0.000149171 | 0.008635 | intron-variant | RFWD2 | GRCh38.p7 | 1:175989359 | GAGGAGAGTAATACT[C/T]ACGCAGAGACAATTT | 64326 |
rs201212494 | in-del | -/AAAGAAAGAAAGAAAGAAAG | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176151354 | GAAGGAAAGAAAGAA[-/AAAGAAAGAAAGAAAGAAAG]AAAGAAAGAAAGAAA | 64326 |
rs201251247 | snp | A/G | 0.00300525 | 0.0386471 | missense, utr-variant-5-prime, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176206789 | ACACAGGCCGCACCG[A/G]GCCCCCGAGGCCGCC | 64326 |
rs201260834 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175952423 | GCAAGACTTCATCTC[A/C]AAAAAAAAAAAAAAA | 64326 |
rs201282411 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176173323 | CTCAAAAAAACAAAA[A/T]GAAAAAAAAAAAAAA | 64326 |
rs201284440 | in-del | -/ATAC | 0.097727 | 0.198275 | intron-variant | RFWD2 | GRCh38.p7 | 1:176141505 | ACTCCATCTCAAAAA[-/ATAC]ATACATACATACATA | 64326 |
rs201307014 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176046490 | AATTAAAAGTTGTTG[A/G]GATTTGTGTAATATA | 64326 |
rs201353528 | in-del | -/AAAATCT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176142729 | GAACAAAAAAAAAAC[-/AAAATCT]CAATGTTCAAGTAAT | 64326 |
rs201358052 | in-del | -/TAA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176026342 | TTGAATACATAATAT[-/TAA]TAATAAAAATAACAA | 64326 |
rs201383226 | in-del | -/AG | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176133763 | TTGCTACTGTTAAAC[-/AG]AGAGGAAAAAGACAA | 64326 |
rs201411126 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176072377 | TGCAAGAAATAAGAC[-/A]GGTAAGGCCCCTGCC | 64326 |
rs201417535 | in-del | -/AA/AACA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176139287 | CAAAAACAAAAAAAA[-/AA/AACA]CAAAAAAAAAAAACA | 64326 |
rs201422094 | snp | G/T | 0.390277 | 0.206936 | intron-variant | RFWD2 | GRCh38.p7 | 1:176002636 | CTTGTGATAGTTTAC[G/T]GAGAATGATGATTTC | 64326 |
rs201428471 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175979499 | AAGTAGATATGCCTT[A/T]AAAAAAAAAAAAGAC | 64326 |
rs201448602 | in-del | -/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176174571 | TTCATAAAAAAAAAA[-/T]TACAGTGAAGAGTAA | 64326 |
rs201456649 | in-del | -/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176124428 | CCCAGCCCCGTACTA[-/C]CCCTTTCCCAGCTTC | 64326 |
rs201462640 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176133919 | AAAGATAACAATATA[C/T]ACAGACCAAGTCATT | 64326 |
rs201478881 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175994356 | GAGCAAAATAACCAG[C/T]TAACATCATAATGAC | 64326 |
rs201505666 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175977039 | CAAAGATATGTTTGG[G/T]GAGTCATGGCATTAC | 64326 |
rs201539205 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176158630 | ACTGTTTTTAAGGTT[C/T]TTTTTTTTTTTTTTT | 64326 |
rs201552818 | in-del | -/A | 0.0111196 | 0.0737302 | intron-variant | RFWD2 | GRCh38.p7 | 1:176015427 | GACACTTTATTAACC[-/A]AAAGTAAAGGGAAGG | 64326 |
rs201563818 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176119667 | ACACACACACACATA[G/T]AGAAAAGAATATTAG | 64326 |
rs201595041 | in-del | -/TAATA | 0.0452528 | 0.143452 | intron-variant | RFWD2 | GRCh38.p7 | 1:176084709 | AATGCTTTGTAAATC[-/TAATA]TATTTTTTCCTATAC | 64326 |
rs201597739 | snp | C/T | 0.000232442 | 0.0107781 | missense | RFWD2 | GRCh38.p7 | 1:176085890 | AAGGCTGTTTCTTTG[C/T]CTAAAATAATAAGAA | 64326 |
rs201644918 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176121519 | TAAATGTCGTTTTTT[A/T]TTTTTATGTTTTTAG | 64326 |
rs201685020 | snp | A/G | 0.00313004 | 0.0394363 | intron-variant | RFWD2 | GRCh38.p7 | 1:176043169 | AGGAGGTGCTGAGAA[A/G]GAGATTCAAACAGTA | 64326 |
rs201685352 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176008277 | GAACCCGGTACCTCA[A/G]ATGGAAATGCAGAAA | 64326 |
rs201701354 | in-del | -/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176095524 | TTTCTATAAAACACA[-/C]AAAAAAAATAAGCTG | 64326 |
rs201734386 | snp | C/T | 1.67851e-05 | 0.00289694 | intron-variant | RFWD2 | GRCh38.p7 | 1:176163026 | CACAACAACTTCCTA[C/T]GAAGACTGTTTTAGA | 64326 |
rs201736713 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176191092 | TTTGTGATTTTATAA[C/T]TTATAATGCCTTTTT | 64326 |
rs201738842 | snp | C/G | 0.129664 | 0.219133 | intron-variant | RFWD2 | GRCh38.p7 | 1:176003632 | CCATTGCTTGTTTTT[C/G]TCAGGTTTGTCAGAG | 64326 |
rs201738854 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175951883 | AAATATATGAAAACG[G/T]TAAGACTAAAATGTT | 64326 |
rs201757466 | in-del | -/C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176112772 | CTCCATGAGATCCAC[-/C/T]TTTTTTTTGGCTCCC | 64326 |
rs201770919 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176129813 | CACATCAATAAGATA[A/G]ATTCAGAAATTTAAA | 64326 |
rs201801126 | in-del | -/AGTT | 0.0236746 | 0.106192 | intron-variant | RFWD2 | GRCh38.p7 | 1:176007643 | TGGGGGGTGTCTCCC[-/AGTT]AGGCTGCTCAGGGGT | 64326 |
rs201803019 | snp | A/T | 0.000115589 | 0.00760138 | missense | RFWD2 | GRCh38.p7 | 1:176046238 | ATATCCACTGCATCC[A/T]GGATGACAGTGTCAT | 64326 |
rs201819264 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176063917 | TAAGTAATGATAAAA[A/C]ATAAAATAGCCACTC | 64326 |
rs201866513 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176058855 | CACGCCTCCTCAGAT[A/G]CCATATGTGAGTTAC | 64326 |
rs201885020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175973111 | TGCTGAGATTACAGG[C/T]GTGAACCACCCCATC | 64326 |
rs201896953 | in-del | -/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176173338 | GAAAAAAAAAAAAAA[-/C]AAAAAACCAGTAATT | 64326 |
rs201905141 | snp | A/C/T | 6.60975e-05 | 0.00574848 | missense | RFWD2 | GRCh38.p7 | 1:175988308 | GCTATATAATCTCCA[A/C/T]TGGAAGCCAGGCCTA | 64326 |
rs201936858 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176054864 | ATACCATAACTTTAC[A/T]AAAAAAAGTTTTCCA | 64326 |
rs201943014 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, missense, utr-variant-5-prime | RFWD2 | GRCh38.p7 | 1:176136506 | CACTCTCTTAATATC[C/G]TCTTCCAAAACACTT | 64326 |
rs201952794 | snp | A/C | 8.24565e-05 | 0.0064204 | intron-variant | RFWD2 | GRCh38.p7 | 1:176027552 | CATCAAAGGAAGACA[A/C]ATCTGCTTTCATTTC | 64326 |
rs201983877 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176127593 | TGTGTGTGTGTGTAT[A/G]TGTATATATGTGTGT | 64326 |
rs202000325 | snp | C/T | 0.000167563 | 0.00915169 | intron-variant | RFWD2 | GRCh38.p7 | 1:175989491 | TGATCTAAAACAAAA[C/T]AAAATTAGATAAATG | 64326 |
rs202035275 | in-del | -/A | 0.0271762 | 0.113356 | intron-variant | RFWD2 | GRCh38.p7 | 1:176087412 | AAAGAAATTTACGAG[-/A]AAAAAATCAACCCCA | 64326 |
rs202036061 | snp | A/G | | | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207641 | TTCGCACGCATGCGT[A/G]ACACGGCTACTCCGC | 64326 |
rs202039310 | in-del | -/AGAAGGAAGGAAAGAAAGAAAAAG | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176151334 | GAAGGAAAGAAAGAA[-/AGAAGGAAGGAAAGAAAGAAAAAG]AAAGAAAGAAAGAAA | 64326 |
rs202042026 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176199395 | TTTTAAAACTAAACA[C/T]ACACTTGGCAGAGAA | 64326 |
rs202046609 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176074807 | AAAAAAAAAAAAAAA[C/T]ATTATTACTCTTTGT | 64326 |
rs202052773 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176087029 | TTCCCTATTTAGTAA[A/G]TGGTTCTGGGAAAAC | 64326 |
rs202064802 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176173324 | TCAAAAAAACAAAAT[A/G]AAAAAAAAAAAAAAA | 64326 |
rs202076118 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175965583 | TTTTTTTTTTGTTTT[G/T]TTTTTGTTTGTTTGT | 64326 |
rs202115838 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176166398 | TCCCAAGTGCTGGAT[C/T]ACAGGCATGAGACAC | 64326 |
rs202135817 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176087172 | AGAAGAAAACCTAGG[C/T]AGTACCATTCAGGAC | 64326 |
rs202142866 | in-del | -/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176079677 | AAAATAATAAAAAAA[-/T]AAAAGTGGTCAGGGA | 64326 |
rs202153223 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175945107 | TCATTGTCAGCTGCA[A/G]ATGTATTTCAGCAGG | 64326 |
rs202185114 | snp | A/G | 0.000516973 | 0.0160692 | intron-variant | RFWD2 | GRCh38.p7 | 1:176163004 | CTAAAAATGAAGAAA[A/G]AAGAAACACAACAAC | 64326 |
rs202194931 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175984709 | GCTGTACCCTGCAAC[A/G]CCACAGTGGTGGAGG | 64326 |
rs207460659 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175946520 | AAAAACAGGTACTCT[C/T]AGAAACACGTACTCC | 64326 |
rs207460660 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176054453 | AGGAATGACCCACTG[C/T]ACCCGGCCAAATTAC | 64326 |
rs207460661 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176111722 | ATTTTGTTCATACTT[C/T]TGGGTTTTTTTCAGT | 64326 |
rs207460662 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176142100 | AAATAAATGATAGAG[A/T]AGTGAGGGGACAAAA | 64326 |
rs367546789 | in-del | -/CCCT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175986559 | ATTCTTTTTCTCCCT[-/CCCT]ATTAAAATACCAGCT | 64326 |
rs367550385 | snp | A/G | | | intron-variant, downstream-variant-500B, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175968288 | AGTTCAGACGGATAC[A/G]GAGGTAACTTTACTT | 64326 |
rs367551115 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176001942 | AGTAATGATTTCTGA[C/T]GAGAAGTCATCAGAA | 64326 |
rs367555493 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175945335 | CATTAATCCTTTTTG[A/G]CCTGCAGCTTAACAG | 64326 |
rs367565076 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175954570 | GGATATCACTAGATA[A/T]TCTATAGATATTAAA | 64326 |
rs367570564 | in-del | -/CGA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176165419 | GTGTAGGAGATACAA[-/CGA]TTTAAAATCAATATA | 64326 |
rs367588037 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175992220 | CTTTGTGTTACAATC[C/T]AATTATACATTTTCA | 64326 |
rs367592782 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176060564 | CTTAACTTTTGAAAC[G/T]GCAAAATAAAATACA | 64326 |
rs367595243 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176027878 | TGCTAATAAAAAGAT[A/G]CCTGAAACTGGGTAA | 64326 |
rs367596790 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176016313 | CAACTGAGAACTATA[C/G]ATGGGAGAGGTGAAA | 64326 |
rs367600121 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176038591 | TTGGGAGGCCAAGGC[A/G]GGCAGATCACAAGGT | 64326 |
rs367603262 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175983838 | TAGCAAAGAGACTGG[C/T]GGCATTTTGCCCCTG | 64326 |
rs367610657 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176005129 | TTCTAGATTTTCTAG[C/T]TTATTTGTGTAGAGG | 64326 |
rs367622905 | snp | A/G | 1.65086e-05 | 0.00287298 | synonymous-codon | RFWD2 | GRCh38.p7 | 1:175988328 | AGCCAGGCCTACAAA[A/G]TTTTTTTCATTGATA | 64326 |
rs367704967 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RFWD2 | GRCh38.p7 | 1:176057387 | CCTCTGATGCCGAGC[A/G]GAAGCTGAACTGTAC | 64326 |
rs367725447 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176064566 | CAGGGTGTATTAAAA[C/T]ATCTAAAACCATTTG | 64326 |
rs367734998 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176045099 | TCCTGGCTCCTCTAT[A/T]TAGCAGGTGTATAAT | 64326 |
rs367738161 | snp | A/G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176202874 | GAGGCAATGATACCA[A/G/T]GTTATGATATTATAA | 64326 |
rs367758396 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176129651 | CCCAGCTGAAGGAGA[C/T]AGAGAAGCTTCAACT | 64326 |
rs367761122 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176144732 | GACCCACACATACAT[A/G]GACACATGATATATG | 64326 |
rs367768907 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176174649 | GGAAAACCATAGCTG[A/G]ATACGTTCAAATTCA | 64326 |
rs367778615 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175985737 | ATAGGTTCTTTTTTT[A/T]AAAATACATACATTT | 64326 |
rs367796613 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176082805 | GCAAAACTCCATCTC[-/A]AAAAAAAAAAGAAAA | 64326 |
rs367801395 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176101116 | GGACATAAGGTGTAC[A/G]TGGGTAAGAGTGAAT | 64326 |
rs367808508 | in-del | -/AC | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176105748 | TTGTTTTGGCGCAAA[-/AC]ACATCAGTTGGTCAG | 64326 |
rs367831566 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175991832 | CACGTTTTGTCTCAC[G/T]GAAAAGTCTTCAAGG | 64326 |
rs367841064 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176177833 | GTTTCGCCCTTCTGG[-/T]TATCAACTACTTTCA | 64326 |
rs367860658 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175997687 | AGAAATGTAAATCAA[A/C]ACCACAATGAGATAC | 64326 |
rs367863130 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176125134 | TAGAATTTTCTAAGC[G/T]CCTCGTATATTCTGG | 64326 |
rs367867939 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:176041601 | TGATCCACCCGCCTC[A/C]ATCTCCCAAACAAAG | 64326 |
rs367873113 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176150792 | GAAAGAAGGAGAAAG[C/T]CCCCAAAATGTCAAT | 64326 |
rs367874107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176181698 | TACAAAAAATTAGCC[A/G]GGCGTGGTGGCACAC | 64326 |
rs367882426 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176077921 | CCACAAAGAAAATAA[A/C]TAGGAACTCATCTAA | 64326 |
rs367914554 | in-del | -/ATCT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176040324 | TTTCCCTCCTTCTCT[-/ATCT]TTCTTTTCTGAGATG | 64326 |
rs367927240 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175996497 | TGTATATCTAGAAAA[C/T]CCCATCGTCTCAGCC | 64326 |
rs367928475 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176083706 | AGTTGGAAATAAAAG[A/T]GAATACAGATGGATT | 64326 |
rs367934365 | snp | A/G | | | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207315 | GGCGTGGCGGGGGAT[A/G]CAACTGGGGACGCAG | 64326 |
rs367935767 | snp | C/T | 1.73033e-05 | 0.00294132 | intron-variant | RFWD2 | GRCh38.p7 | 1:176206556 | GGGACAAGGAGGGAG[C/T]GCTCTTCAAACCCAC | 64326 |
rs367949634 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176200121 | TGGGCCACATTTCCT[C/T]ATCTACAAAATGGGA | 64326 |
rs367964414 | in-del | -/A | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:176029445 | TCATTTTTCAACAAT[-/A]AAAACAGTAAGACAG | 64326 |
rs367965663 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176025864 | CACTGTACTCAACCT[A/G]GGTGACCCTGTCTCA | 64326 |
rs367972081 | in-del | -/G | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176027744 | AATACATTAGTAAAT[-/G]CTTCTGTAACTTGGG | 64326 |
rs367978902 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175993532 | AACTAGAATAACCAA[C/T]ACAGAGAAGTGCTTA | 64326 |
rs367986943 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175955217 | ACTGTACTCTCGCCT[C/G]GGTGACAGGAGTGAG | 64326 |
rs367998234 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176032920 | ATACTTAGTAAAGCT[G/T]TAACTTATAGGAAAG | 64326 |
rs367999772 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176093955 | TTTAACCCAGGAAGC[A/G]GAGGTTGTAGTAAGC | 64326 |
rs368005834 | in-del | -/ACA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176079458 | GTAAACATGGGAACA[-/ACA]CATACCGGGGACAAC | 64326 |
rs368007889 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176016866 | TAAACAGACAAAGAA[A/T]CTGCCAGTCTAGGAA | 64326 |
rs368038746 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176161104 | CTCCCTATTGCTGGT[A/G]TAGCATTCAGTTTCC | 64326 |
rs368056922 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176039249 | GGGAAATTTAAAATA[A/T]TCAGAACTAAGTGAA | 64326 |
rs368057576 | in-del | -/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176025895 | TAAAAACAAAAAAAC[-/C]AAAAAAAAAGAAAAC | 64326 |
rs368063057 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176012415 | ATAGATGTAAGCCAC[C/T]GCACCCAGCCAAGCT | 64326 |
rs368094131 | in-del | A/TT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176025617 | GAAAACAACCCAAAC[A/TT]ATAGCCAGGGCGCAG | 64326 |
rs368107140 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant | RFWD2 | GRCh38.p7 | 1:176136429 | CAACTTAATGGAAAG[A/G]TGACAATTTCATGAA | 64326 |
rs368107900 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176156019 | GGTAAATAAAAAAAG[A/G]GTCTGGTGGGTTTTT | 64326 |
rs368120390 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176101475 | AGTAATCGTGTCTTT[G/T]TACTATGGGACACTC | 64326 |
rs368135419 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176098436 | ATTAGATAAGATAAA[C/G]CTAAAAGTTTAACAG | 64326 |
rs368140696 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176203671 | CCTGTATTAGATTCT[C/G]CATCAATAAAACACT | 64326 |
rs368142041 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176130368 | CCAATCTCTAATTTT[A/C]TCATTATTTCACACA | 64326 |
rs368148128 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176143384 | AAAACTTCCCGCAAA[A/C]AATCACAGGTCTAGA | 64326 |
rs368161507 | snp | A/C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176116748 | AACAGAAAAAGTAAA[A/C/T]CTAAAGTATATCATA | 64326 |
rs368177478 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175982859 | GAATAGAATGGTAGT[C/T]ACCAGAGGTGGGGGA | 64326 |
rs368231272 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176053004 | ACTGTTAAACAATGC[C/T]GGGGAAAAAAAAAAC | 64326 |
rs368248342 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175998690 | TCATAATGTACAATA[G/T]TCCAGAGATGATTTT | 64326 |
rs368254247 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176021407 | AATTATCTAAAGATA[C/T]TACATATTTATTTTG | 64326 |
rs368259396 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175992302 | CAGCTCCAGTCTACA[G/T]CTCCCAGAGTGAGCG | 64326 |
rs368277289 | snp | C/T | 0.000134307 | 0.00819363 | intron-variant | RFWD2 | GRCh38.p7 | 1:176046130 | CATGATAATTACATA[C/T]GCAAATTGTTACATC | 64326 |
rs368355116 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176007817 | TGTGTGCCCTGTCCC[C/G]AGAGGTGGAGCCTAC | 64326 |
rs368366719 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176105199 | GCTGAAAGGGTAGCC[A/G]TTATTGATTATAACT | 64326 |
rs368379401 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176019182 | TAAAAAAATAAATCA[C/T]GGCCGGGTGTGGTGG | 64326 |
rs368392595 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176002913 | TATTTCTAGTTCTAG[A/G]TCCCTGAGGAATCGC | 64326 |
rs368392736 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176060318 | TTTCTCCTTAAAGCA[C/T]TTAAAGATGCCCTTT | 64326 |
rs368393533 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | RFWD2 | GRCh38.p7 | 1:176113311 | TAGTGATAAGTATTT[G/T]TACATATACCTATTG | 64326 |
rs368484018 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175997405 | TGACAAATGGGATCT[A/G]ATTAAACTAAAGAGC | 64326 |
rs368490690 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176006387 | TGAATTTGATCCTGT[C/G]ATTATGATGTTAGCT | 64326 |
rs368508535 | in-del | -/TC | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176070126 | CCTCCAGTATCCCCA[-/TC]TCTGTAAATGATACC | 64326 |
rs368524592 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176063719 | TAGGTTAGCTTTTGT[C/T]TTATTTCAGGGCATT | 64326 |
rs368527441 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176203758 | AAATGCAACCTAAAC[A/C]CCTAAAATGTTTATG | 64326 |
rs368535260 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176083701 | TTAATAGTTGGAAAT[A/G]AAAGAGAATACAGAT | 64326 |
rs368541800 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176063152 | GCAAGCTCCGCTTCC[C/T]GGGTTCACGCCATTC | 64326 |
rs368579580 | snp | A/C | 0.00022902 | 0.0106985 | intron-variant | RFWD2 | GRCh38.p7 | 1:175945205 | GATCCATTTAATAAA[A/C]TCATTTAAGATATAA | 64326 |
rs368580094 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176004501 | GTTTGTCATAGATAG[C/T]TCTTATTATTTTGAA | 64326 |
rs368583323 | in-del | -/C | 0.000577601 | 0.0169843 | intron-variant | RFWD2 | GRCh38.p7 | 1:175947251 | ACTCCTAGAAAAGAA[-/C]AAGAGCTTTTAAAGT | 64326 |
rs368588582 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176050837 | TAAGTAATTTGTCCA[C/T]GGATACACCAGATAA | 64326 |
rs368596555 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176127064 | CAAATATATCCCAGC[A/G]CCTAACAGTGTTTTT | 64326 |
rs368598379 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176106054 | TTGTTTTTTTGAGAC[A/G]GAGTCTCGCTCTGCT | 64326 |
rs368607299 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | RFWD2 | GRCh38.p7 | 1:175989327 | AAGTACAGAGCTCTG[C/T]ATTAAGCTCAACCTC | 64326 |
rs368608409 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175983526 | TTGAGTATATCTTTA[C/T]CAGCAGTGTGAAAAT | 64326 |
rs368612568 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176194217 | ATCCCAAAAGCAAGA[A/C]AGGAAGAAAAAAAGA | 64326 |
rs368625989 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176118365 | TTTTTTTTTAAGGCA[C/T]AGTTAATGGGTACAA | 64326 |
rs368629355 | in-del | -/AG | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176176382 | ACCCTTAATACTCAG[-/AG]TTCATTGAAATAAAA | 64326 |
rs368648300 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176075678 | AAACAAGTTATTCTC[A/G]GCTTACAAGAAGACT | 64326 |
rs368653098 | in-del | -/GT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175959950 | TTTATCTTGTTTTGT[-/GT]TTCAGGTTTAACAAA | 64326 |
rs368655103 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175993623 | AGGAGCCGATGAGAT[C/G]AACTGGAAGAAAGGG | 64326 |
rs368658119 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175956379 | AAAATTAATTCTAAA[C/T]AGATCTAAGACATAC | 64326 |
rs368658167 | in-del | -/ATA | 0.0158469 | 0.0875917 | intron-variant | RFWD2 | GRCh38.p7 | 1:176131720 | ATAGTATTATAAAAG[-/ATA]ATATTTGTCTCAGAA | 64326 |
rs368670457 | snp | C/T | 7.07164e-05 | 0.00594585 | intron-variant | RFWD2 | GRCh38.p7 | 1:175986905 | ACATAATGCATAATA[C/T]GAGATCCCAAGGTGA | 64326 |
rs368671990 | snp | C/T | 0.000148413 | 0.00861305 | intron-variant | RFWD2 | GRCh38.p7 | 1:176027554 | TCAAAGGAAGACAAA[C/T]CTGCTTTCATTTCTT | 64326 |
rs368693583 | in-del | -/AGTCT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175984718 | GCAACGCCACAGTGG[-/AGTCT]TGGAGGTCTCCAAGA | 64326 |
rs368705243 | snp | A/G | 0.000386658 | 0.0138989 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176206700 | GCCGGCGCTGGGCCT[A/G]GCCGCGCAGCTGTGC | 64326 |
rs368726984 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175978640 | CATGCTCAGAATCTG[C/G]TTTCATTCTACTCCC | 64326 |
rs368730232 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175956707 | TGGGTCACATATATG[A/G]TGGTGGTCCAATAAG | 64326 |
rs368747493 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176136933 | TTTTTTTTTTAAATA[C/G]AGATAGGTTTCACTA | 64326 |
rs368756427 | in-del | -/AAAAAAG | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176082810 | AACTCCATCTCAAAA[-/AAAAAAG]AAAAAAGAAAAAAGA | 64326 |
rs368762781 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176011662 | TATGGCTAGAGAGAA[A/T]TTAGAAATATAACAC | 64326 |
rs368769265 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176170966 | CCATCTCTACTAAAA[A/T]TACAAAAAATTAGCC | 64326 |
rs368799752 | snp | A/G | | | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207794 | TCCGAGCGGTTGCAG[A/G]CAGCACTGCATTGAG | 64326 |
rs368806572 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176100550 | ACAGTAGTTTCCAGC[G/T]GCAGCTCAGAAAAAA | 64326 |
rs368819580 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176089278 | AGCCTGGGTGACAGA[C/G]TGAGACTCTGTCTAA | 64326 |
rs368825871 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176004579 | GTTGTTGCATTTTGT[C/T]GAAGGCTTTTTCTGC | 64326 |
rs368839801 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176057162 | AAGTAGGTGTAAGAA[A/T]CTTATTATCCATTAT | 64326 |
rs368859421 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:176204453 | CAGCCAAACGGGGGG[A/G]AAAAAAAAGAAAAAA | 64326 |
rs368859772 | snp | C/T | 1.65548e-05 | 0.002877 | intron-variant | RFWD2 | GRCh38.p7 | 1:176134989 | ATGAATTCTAATCAA[C/T]TGCAAGTGTGAAGCT | 64326 |
rs368879009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175972760 | TGTAAGCCACTGCTC[C/T]CAGCCAAAAATGACA | 64326 |
rs368885914 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176083710 | GGAAATAAAAGAGAA[A/T]ACAGATGGATTTACA | 64326 |
rs368896791 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176007952 | CCCAGCCTCGCTGCC[A/G]CCTTGCAGTTTGATC | 64326 |
rs368899778 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175993736 | CCTCCAAGAAATATG[C/G]GACTATGTGAAAAGA | 64326 |
rs368903582 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176205063 | TGACAATGATCGATT[C/T]CTTATTCCTCACATC | 64326 |
rs368939652 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176105651 | TGACCTCAGCTTGTA[C/T]GGACTGACCACTGAC | 64326 |
rs368946187 | in-del | -/AAT | 0.0178098 | 0.0926698 | intron-variant | RFWD2 | GRCh38.p7 | 1:176157214 | AATAATAACAACAAC[-/AAT]AATATTAATATTAAC | 64326 |
rs368948132 | snp | C/T | 4.94531e-05 | 0.00497234 | intron-variant | RFWD2 | GRCh38.p7 | 1:176081149 | AATTTGACCAATACT[C/T]ACCTAGAGACTATAC | 64326 |
rs368957051 | snp | A/C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176195766 | GGAGTCCATTATCCT[A/C/G]AACGGATTAACACAA | 64326 |
rs368974044 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175962763 | CTCACCGCACCTCCC[A/C]CTCCCTGGGCACCTA | 64326 |
rs368981311 | in-del | -/AAGA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176188942 | CACAGATGACAGAGA[-/AAGA]GTTAGGAAAAAATAT | 64326 |
rs369013460 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175975128 | AACAGTTTCATTCTT[A/G]GTAACTCTGGTTGAT | 64326 |
rs369024093 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | RFWD2 | GRCh38.p7 | 1:175989715 | GTTTTAATGATGTCA[C/T]GAAAAAAATGTTAAT | 64326 |
rs369034652 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176003424 | ACATGAAGTCCTTGC[C/G]CATGCCTATGTCCTG | 64326 |
rs369057317 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176023817 | AATAATCCAAGCCCA[A/G]ACAGTTTCTCTAATG | 64326 |
rs369091129 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176062036 | ACGGCATCTCACTCT[A/G]TCGCCCAGGCTGGAG | 64326 |
rs369113012 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176131688 | CATACTATTGCTTAA[A/G]GAAAAATCAAATATG | 64326 |
rs369120226 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175957695 | GGTATTTATCCAAAA[G/T]AAATGATGGTATATA | 64326 |
rs369148015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176198758 | TAAAGAACACTTACA[A/G]CGCAAGATGACATGC | 64326 |
rs369159247 | in-del | -/TATAAGTT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176106455 | TATAGTTTATAAGTT[-/TATAAGTT]AGGCAGCTGGAGGCT | 64326 |
rs369162169 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176007272 | CAATGTTTTCAACTT[C/G]TTTGCCTTTGGTTTG | 64326 |
rs369179905 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176003493 | TTTTAGGTCTAACAT[G/T]TAAGTCTTTAATCCA | 64326 |
rs369196629 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175993802 | TGGGGAGAATGGAAC[C/G]AAGTTGGAAAACACT | 64326 |
rs369198515 | in-del | -/CTCAGG | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176096362 | AGGCTCAGGCTCAGG[-/CTCAGG]ATGGTTGGGCGAATG | 64326 |
rs369201844 | snp | C/T | | | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176209010 | CTTGAACCCAGAAAG[C/T]GGAGGTTGGAGTGAG | 64326 |
rs369207585 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176083405 | TTTCAACAGAAACCA[C/T]AAAGAAAACAATAAA | 64326 |
rs369210360 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176049002 | AAGGTGAAACCCCGT[C/T]TCTACTGAAAATACA | 64326 |
rs369244875 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175946493 | CTACCAAATCAGCAG[A/G]GAATATGTGGAAAAA | 64326 |
rs369251341 | snp | A/T | 0.000153988 | 0.00877328 | intron-variant | RFWD2 | GRCh38.p7 | 1:176162843 | TTCATCATTTAAAAT[A/T]TTTTTTAAGTTTAGC | 64326 |
rs369300606 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176049125 | TGCAGTGAGCCGAGA[C/T]TGCGCCATTGCAGTC | 64326 |
rs369311672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176101715 | CACTTATTTTGTTTT[A/G]ATACATGTTTTCTAA | 64326 |
rs369321918 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176184315 | CCCACAAGTGAGTAA[C/T]TAGTGCTTCATGGTT | 64326 |
rs369332609 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176036935 | ATCTTGTAACAAATA[A/T]AATGTATCGATTCCC | 64326 |
rs369385965 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176021102 | TCCCCCTGCTTCAAC[C/T]TCCCAAAGTGTTGGG | 64326 |
rs369392819 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176121143 | CTTTTTCCTTTCCAG[G/T]ACTCTACATATAGTT | 64326 |
rs369412609 | snp | A/C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176150588 | CTACGATTATTTGTC[A/C/T]AGAGGACAAAGACCA | 64326 |
rs369426390 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176203320 | CCAGCCTGGGCAGCA[A/G]AGCGAGACTCCGTCT | 64326 |
rs369426728 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176181668 | TAACATGGTGAACCC[C/G]GTCTCTACTAAAAGT | 64326 |
rs369463611 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175983148 | CCCCATAAATACTTA[C/G]AATTATTATTTGTCG | 64326 |
rs369471153 | snp | C/T | 6.60186e-05 | 0.00574499 | synonymous-codon | RFWD2 | GRCh38.p7 | 1:176085861 | TCGTCTTGATGCTAA[C/T]GTGCTATTATACCAA | 64326 |
rs369479442 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175995516 | AAGACTAATAAAGAA[A/G]AAAAGAGAGAAGAAT | 64326 |
rs369502312 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175964360 | CCAACAAAAATCAGA[A/G]ATGTTTTCTCCCCTA | 64326 |
rs369503346 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176077223 | AGATACAAAAATCCT[C/T]GACAAAATACTCTGT | 64326 |
rs369507225 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176086370 | AGCTGGGACTACAGC[C/T]GCCCGCCACCACGCC | 64326 |
rs369549398 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176005526 | ACACTGCTTTGAATG[C/T]GTCCCAGAGATTCTG | 64326 |
rs369567254 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176125750 | AGGATTTTTTTTTCT[A/G]TTTCTGTGAAGAATG | 64326 |
rs369577270 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176158840 | GAGACAGGGTTTTAC[C/T]ATGTTGCCCAGGCTG | 64326 |
rs369587337 | snp | A/G | 0.000364516 | 0.0134954 | intron-variant | RFWD2 | GRCh38.p7 | 1:176184583 | TGGCTACATTTACAG[A/G]TAAGTTTTAAAATGT | 64326 |
rs369613848 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176111148 | CAGAGCGAGACCTTG[A/T]CTCAAAAAATAAAAA | 64326 |
rs369639647 | snp | A/G | 9.44465e-05 | 0.00687127 | intron-variant | RFWD2 | GRCh38.p7 | 1:176163770 | AAACCAATAAAAACA[A/G]CAAAATGAAATTTAT | 64326 |
rs369642237 | in-del | -/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175973419 | CATGAAAATAAAATA[-/C]ATGAAGTCAGCATAA | 64326 |
rs369648015 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175947559 | ATTTTTAGTAGAGAC[A/G]GGGATTCTCCATGTT | 64326 |
rs369648715 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176194924 | CTACAAAATAAAATT[A/T]AAAAAAAAAAAAATC | 64326 |
rs369652067 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176053018 | CTGGGGAAAAAAAAA[-/A]CCCCTTCTATATGTG | 64326 |
rs369656749 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176061575 | AGGTTGCAGTCAGCC[A/G]TGATCACGCCATTGA | 64326 |
rs369664005 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176004668 | TTTATTGATTTGTGT[A/G]TATTGAACCAGCCTT | 64326 |
rs369666942 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176198028 | TAATTGGAGAAATAT[A/C/G]CTATGTTCATGATTC | 64326 |
rs369674298 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175983884 | GAACTCTGTCCTTGA[C/G]AGAGATGAGTTAGGG | 64326 |
rs369680816 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175999398 | TTCACTTTACATAAT[G/T]ATCTCCAGTTCCATC | 64326 |
rs369705740 | snp | A/G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176110564 | TAGATTGGAAACTTC[A/G/T]TTATAGCAAGGATTA | 64326 |
rs369711976 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | RFWD2 | GRCh38.p7 | 1:176003274 | CAGATGAGTAGGTTG[C/T]AAAAATTTTCTCCCA | 64326 |
rs369717617 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176131730 | AAAAGATAATATTTG[G/T]CTCAGAATGTCTGAT | 64326 |
rs369726649 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175980974 | TTTGTATACTTAAAA[C/T]ACTTCATATTTCATT | 64326 |
rs369745138 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176117712 | CCAGCCTGACCAACA[C/T]GGTGAAACCCTGTCT | 64326 |
rs369753586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176156735 | TAATAAAGGAGATGA[C/T]TCATCCAGAAGATAT | 64326 |
rs369757291 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176041775 | GTTCGAGACCAGCCT[A/G]GCCAGCACGGTGAAA | 64326 |
rs369788895 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176179644 | CAGGAGGCTGAAGCA[A/G]GAGGATTGCTTGAGC | 64326 |
rs369814625 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176089930 | TGCATCTGTATTAAC[A/G]TAACTACACCCTTCC | 64326 |
rs369822628 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176007217 | TTTAAGCACTTCTCT[A/G]TATTGGTTATTCTAG | 64326 |
rs369828775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176125554 | TGTGTGGATTTGTTT[C/T]GGGGTCCTCTATTCG | 64326 |
rs369829424 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175995573 | ACGGGATATCACCAC[C/T]GATCCCACAGAAATA | 64326 |
rs369850668 | in-del | -/TGA | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176185158 | GCTTGTAGGTAATGA[-/TGA]CAACAATCATAACAA | 64326 |
rs369854636 | in-del | -/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176038702 | GTGCGCCTGTAATCC[-/C]AGCTACTCAGGAGGC | 64326 |
rs369887649 | in-del | -/ATATAT/ATATATAT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176028696 | TGGTATATTTGTTTC[-/ATATAT/ATATATAT]ATATATATATATATA | 64326 |
rs369894015 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176089293 | CTGAGACTCTGTCTA[A/T]AACAATAACAACAAC | 64326 |
rs369931099 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176084933 | GCACCCAACATGTAC[C/T]AAGCATTGTATCTTA | 64326 |
rs369948695 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175996736 | ACAAACCACTGCTCA[A/G]TGAAATAAAAGAGGA | 64326 |
rs369949887 | snp | A/G | 2.09558e-05 | 0.00323689 | intron-variant | RFWD2 | GRCh38.p7 | 1:176046375 | AATTTGCTATTTTCT[A/G]TTTCTAAAGTAATTC | 64326 |
rs369955753 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176005649 | TGTTCAGTTTCCATG[A/T]AGTTGAGCGGTTTTG | 64326 |
rs369958055 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176145741 | AGGAATAAAAGATTA[A/C]ATACTGCACAAGCAC | 64326 |
rs369968894 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | RFWD2 | GRCh38.p7 | 1:176058086 | CCGGGAGGGAGGTGG[A/G]GAGGTCAGCCCCCGC | 64326 |
rs369983605 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176107605 | AATAAATGTGGAAGA[C/T]ATAAAAACTCAGAAA | 64326 |
rs369991055 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176124250 | CTCAAGCATTTATCC[C/T]TTGTGTTACAAACAA | 64326 |
rs370004147 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176023631 | GCTGAGGCAGGAGAA[C/T]TGCTTGAACCCAGGA | 64326 |
rs370008046 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176054247 | CTCACTGCAACCTCC[A/G]CCTCCCAGGTTCAAA | 64326 |
rs370017503 | snp | A/G | 2.03938e-05 | 0.00319319 | intron-variant | RFWD2 | GRCh38.p7 | 1:176149092 | ACAATAGAAAATTAT[A/G]ATTTTTCTTTTAAAA | 64326 |
rs370018116 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176172949 | AAATGTTATTTCCAC[A/G]GTTGACAACAATATA | 64326 |
rs370029601 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176175076 | TCCATGTATTCCTTC[C/T]CAAGTTCTTAATTTT | 64326 |
rs370032340 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176162696 | GTATTGAAATTGTTC[C/T]TTAAGTTACAAAAAG | 64326 |
rs370052661 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176188868 | ACACACAGACAGAGA[A/G]CAAAGCATCCCAGAG | 64326 |
rs370088886 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176006145 | GTTGGTTTAAAGTCT[G/T]TTTTATCAGAGACTA | 64326 |
rs370091759 | snp | A/C | 1.69235e-05 | 0.00290886 | missense, intron-variant, utr-variant-5-prime | RFWD2 | GRCh38.p7 | 1:176163858 | AACCTCTTTTCCTCA[A/C]ATCTTTGCTTCTGTT | 64326 |
rs370093591 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176103512 | CATCCTCTTCCCTAC[C/T]TTGGAATATTTGCAT | 64326 |
rs370147715 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176071224 | TGTGGTACCTCCCCC[C/T]TCACTCTCTCTCACT | 64326 |
rs370157085 | in-del | -/ATTA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176008454 | ACTTTCAACAACAGA[-/ATTA]TTTGTTTTTATTTCT | 64326 |
rs370168070 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175962913 | TTAATGATTATATCC[A/G]CAAACATAGTTCAAG | 64326 |
rs370208213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175984965 | ATTTTACAGACTCAT[A/G]GGCAGAAGGGACTTG | 64326 |
rs370215801 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175995863 | AACTATTCCAATCAA[C/T]AGAAAAAGAGAGAAT | 64326 |
rs370216084 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176134561 | CCAAGGAAATCTAAA[C/T]TAACAGATCTGTCTA | 64326 |
rs370223094 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175976967 | GAGAAATAAAAAACA[C/G]TTAAAGCAAAATCAA | 64326 |
rs370227305 | in-del | -/AATT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176204566 | AATCAGATTCTCATT[-/AATT]AATTCTTCTGAATAT | 64326 |
rs370229966 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176152886 | TATTACTATTTAGGT[A/T]ATAATTTTTCTCTAG | 64326 |
rs370266966 | in-del | -/TGTCAA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175980286 | ACACAAATACAATAC[-/TGTCAA]AAGACAGTATATTAA | 64326 |
rs370279659 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175950593 | AGTTCTAGCTCAACA[C/G]GTTATTTTTTACTTG | 64326 |
rs370286964 | snp | A/T | 0.000153988 | 0.00877327 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176184696 | AAGCAGATGGGGCTA[A/T]AAAGAAAAGAAAAAT | 64326 |
rs370287338 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207217 | CGCTGTCGAGGCCGC[C/T]GCCGCCACCGCGGTC | 64326 |
rs370290962 | snp | G/T | 6.24174e-05 | 0.00558613 | intron-variant | RFWD2 | GRCh38.p7 | 1:176135120 | GAATTATAGTAGATA[G/T]TTCAAATAGAAGATA | 64326 |
rs370303352 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RFWD2 | GRCh38.p7 | 1:176055673 | GCATAGTTAACCCGT[C/T]CAAAATTGAGTTTCT | 64326 |
rs370317710 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176074819 | AAAGATTATTACTCT[C/T]TGTATAGTCACATAA | 64326 |
rs370331393 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175985303 | CTCTTTTACTATGTC[C/T]GTTTATTTTTTATTG | 64326 |
rs370333684 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176004394 | CAACACTATGTTGAA[G/T]AGGAATGGTGAGAGA | 64326 |
rs370360485 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176041099 | TATATGATGAACTTC[C/G]TTAAGAGATTTTAGT | 64326 |
rs370392456 | snp | A/C | 3.42495e-05 | 0.00413807 | intron-variant | RFWD2 | GRCh38.p7 | 1:176085938 | ATAAACAATACTCTT[A/C]TTTTGCACAGAATAC | 64326 |
rs370410274 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176203624 | CCTCTGAATGTTGAA[A/G]ATGTATCCAATGTCA | 64326 |
rs370415438 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176203273 | ACCCGGGAGGCGGAG[C/G]TTGCAGTGAGCCGAG | 64326 |
rs370418947 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175994500 | GTATTCAGGAAACCC[A/G]TCTCACGTGCAGAGA | 64326 |
rs370442945 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175960394 | GATCAAACAGACACA[C/T]ACATAAGTGCCTGGC | 64326 |
rs370449971 | snp | C/T | 3.37872e-05 | 0.00411004 | utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175945129 | TTCAGCAGGATCAAG[C/T]ACAATTTGACTTGAG | 64326 |
rs370469018 | snp | C/T | 1.654e-05 | 0.00287571 | intron-variant | RFWD2 | GRCh38.p7 | 1:176116723 | ATTTCAGTATTTACA[C/T]TATTTTAACAACAGA | 64326 |
rs370471978 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176169781 | AAAGAACACAATGAC[A/G]AAGACTGCTGCATCA | 64326 |
rs370488224 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175960419 | CCTGGCATAAAGTAT[A/G]TATCTTATAAGTGAT | 64326 |
rs370493657 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175990324 | TTTGTATGTCTTCAA[G/T]CATTTTAAATTTATT | 64326 |
rs370535479 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176135498 | AGATAACTGGATCAT[C/G]AGGTTCAACTCTTGA | 64326 |
rs370585976 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176015216 | AGATCAAAGCAGGAA[A/C/T]GCAGGATAAATTTAT | 64326 |
rs370588278 | snp | A/G | 0.105924 | 0.204309 | intron-variant | RFWD2 | GRCh38.p7 | 1:175995998 | ATGCAAAAATCCTCA[A/G]TAAAATACTGGCAAA | 64326 |
rs370599718 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | RFWD2 | GRCh38.p7 | 1:175966646 | GCAAAATGGAAGAAA[A/G]AAGAAAGGTGTCTTG | 64326 |
rs370601607 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176048214 | TTTTTTTTTTTTTTT[A/T]CAGAGATGGGGTCTC | 64326 |
rs370607031 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176039592 | ACAGAAAAAAAAAAA[A/T]TTACCTTAAAATTCA | 64326 |
rs370607792 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176018255 | GAAGTAGCAATTACT[C/T]ATCTGCACATTAGAT | 64326 |
rs370613965 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176062415 | GATAAGGGAAAAGCA[C/T]AGAAAAACAATGAGA | 64326 |
rs370627066 | snp | A/G | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176186130 | CAGAGCAGGAGGAAC[A/G]GCAAAAGAACCAACC | 64326 |
rs370639924 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175949294 | CACTTCCATATTCGG[C/G]GTGGGGGGCTGGGGT | 64326 |
rs370651783 | in-del | -/ATAA | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176145763 | CACAAGCACACTTAA[-/ATAA]CGCTCAAAAACAGAG | 64326 |
rs370664619 | in-del | -/GACA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175977687 | AGTTTCTTTTCCCCA[-/GACA]ATCTGTATATTCTTA | 64326 |
rs370685220 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176117738 | TGTCTCTACTAAAAG[C/T]AAAAAAATTAGCTGG | 64326 |
rs370731534 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176143123 | ATCCAACAGAACAAG[A/C]GAGAGAGAGAGAGAG | 64326 |
rs370737079 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176166823 | ATGCCTGAATTCCCC[A/G]CTACTCAGGAGGCCT | 64326 |
rs370764534 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176007341 | AGCCTTCTTCTCTCA[A/G]CTCGTCAAAGTCATT | 64326 |
rs370776169 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176042351 | GGGCAGATCACTTGA[A/G]GTCAGTTTGATACCA | 64326 |
rs370798304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176086924 | AGATACAGACCAATC[A/G]AACAGAACAGATGCC | 64326 |
rs370819418 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176054353 | TTTTAGTAGAGACAG[A/G]GTTTCACCATGTTGG | 64326 |
rs370820990 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175960759 | CTTTGACAGAGGCTT[C/T]GCCAGAAAGCTACTC | 64326 |
rs370841032 | snp | C/T | 0.000197928 | 0.00994611 | synonymous-codon | RFWD2 | GRCh38.p7 | 1:175947237 | AATCAGCACATTGGA[C/T]TCCTAGAAAAGAACA | 64326 |
rs370843695 | in-del | -/A | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176121055 | TTTTACGTTTATAGC[-/A]AAAAAAAATCAATGA | 64326 |
rs370845246 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | RFWD2 | GRCh38.p7 | 1:176004961 | CCTCTGGTAGAATTC[A/G]GCTGTGAATCCATCT | 64326 |
rs370866173 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | RFWD2 | GRCh38.p7 | 1:175953734 | CAGCGATAAAGACAG[C/G]TATTTCATAATTAAA | 64326 |
rs370872747 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175985609 | TATAAGCACTTTCAC[C/T]CACCCCACCAGAACT | 64326 |
rs370876622 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176027936 | AATTGACTCACAGTT[C/T]CACACGGCTGAGGAG | 64326 |
rs370920340 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176073709 | TTTAATAGTCGAGAT[A/G]CTGTCAAAGTAAACA | 64326 |
rs370930578 | in-del | -/TCTCCC | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176057332 | CCCTCTCCCTCTCCC[-/TCTCCC]CACGGATTCCCTCTC | 64326 |
rs370980626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176007394 | GCTGGTGAGGAACTG[C/T]GTTCCTTTGGAGGAA | 64326 |
rs370982543 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175972681 | ATGTTGGCCAGGCTG[A/G]TCTCAAATCCCTGAC | 64326 |
rs370987275 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175985353 | ACAAAACTAAAAAAA[-/A]TAAAGCACTTAGATG | 64326 |
rs370990996 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176110969 | CCATCCTGGCCAACA[C/T]GGTGAAACCCCGTCT | 64326 |
rs370996928 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | RFWD2 | GRCh38.p7 | 1:176170609 | GAAAAGAGATATGCT[C/G]TCTTCAGGCTTTGTT | 64326 |
rs371021408 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176019146 | ACTCCAGCTTGGGCA[A/T]CAGAGCGAGAATAGA | 64326 |
rs371033790 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176006118 | TGGCCTTCTTTGTCT[C/G]TTTTGATCTTTGTTG | 64326 |
rs371036347 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175990940 | CCCATTCTGCCAATC[C/T]CTGAATGTTACAACA | 64326 |
rs371042637 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175997339 | GGACATAGGCATGGG[A/C]AAGGACTTCATGTCT | 64326 |
rs371044540 | snp | C/G | 1.72365e-05 | 0.00293563 | missense, utr-variant-5-prime | RFWD2 | GRCh38.p7 | 1:176206592 | GAAGTCGTTGCTTTT[C/G]TCCTCGTAGGAGTTG | 64326 |
rs371048258 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176088359 | TACAAAATTTCATTA[C/T]ATAAGGATTAAAAAC | 64326 |
rs371055708 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176111692 | TACATTTTATTTATA[C/T]GAAAAAAACTGTCTA | 64326 |
rs371113275 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175994098 | CAATATTCAACATTC[C/T]TAAAGAAAAGAATTT | 64326 |
rs371116201 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176086864 | CTTCAAACTATACTA[C/T]AAGGCTACAGTAACC | 64326 |
rs371124616 | in-del | -/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176204452 | ACAGCCAAACGGGGG[-/G]AAAAAAAAAGAAAAA | 64326 |
rs371130935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176024917 | TTACAAAACTATTGA[C/T]GATAAAAATGGCAAA | 64326 |
rs371131657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176173815 | CAACATGGTGAAACC[C/T]CGTCTCTACTAAAAA | 64326 |
rs371136578 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176005059 | TACTCAGAGATTCAA[C/T]TTCTTCCTGGTTTAG | 64326 |
rs371173662 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175997573 | AACAAACAACCCCAT[C/G]AAAAAGTGGGCGAAG | 64326 |
rs371184920 | snp | A/C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207947 | CGACCACGACTTCAC[A/C/T]CCTATATTTTGAAAA | 64326 |
rs371188008 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176009421 | CATATAATAATATAC[C/T]AACGTATTCTCATGT | 64326 |
rs371215731 | in-del | -/CAAG | 0.0154538 | 0.0865337 | intron-variant | RFWD2 | GRCh38.p7 | 1:176132204 | CTCCACACAGGGATC[-/CAAG]TAAACATTTTAAAAT | 64326 |
rs371221122 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175958213 | AAAAAGCTGGGAACA[A/C]ACACACAAGAACAAA | 64326 |
rs371221614 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176141425 | AGAATCTCTTGAACC[C/T]GGGAGGTGCAGGTTG | 64326 |
rs371234808 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175976075 | ATTAGAAGGTCTCAA[A/T]GGTCTCAATCCTTTA | 64326 |
rs371235730 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176120413 | TGCTGGGTGACAGGG[C/T]AAGACTCTATCTCCA | 64326 |
rs371239372 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176096127 | AGTTGTGTGACAAGA[G/T]CCTGGTTTTAGCTGA | 64326 |
rs371240219 | snp | A/G | 1.65132e-05 | 0.00287339 | synonymous-codon | RFWD2 | GRCh38.p7 | 1:176027624 | GCTGAATTTAACACA[A/G]CACACATTAGCCTTT | 64326 |
rs371273801 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176082729 | AGAATAGCTTGAACC[C/T]GGGAGGTGGAGGTTG | 64326 |
rs371281318 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176129453 | ATTTTTTAAAAAAAA[A/T]GAATTAAACTTTCAA | 64326 |
rs371281669 | snp | C/T | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176185476 | CAGAATACTCAAAAT[C/T]CCAGCCTTTTTTGTA | 64326 |
rs371289151 | in-del | -/TAAA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176165702 | AAATAAATAAATAAA[-/TAAA]CAAGTAAGTAAGTAA | 64326 |
rs371293010 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176162836 | AATAAAGTTCATCAT[C/T]TAAAATTTTTTTTAA | 64326 |
rs371295278 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176183529 | ATAGTGCAGCCCCTA[C/T]AGAAAACAGTATGGC | 64326 |
rs371308414 | in-del | -/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175965760 | ACCCAGCTAATTTTT[-/T]GTATTTGGAGACGGG | 64326 |
rs371317947 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176178984 | GAATTTTTTTTTTTT[A/T]GTTTTTTTTTTTAAA | 64326 |
rs371330853 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176029468 | TAAGACAGGATACAC[A/C]CATAAAATAGATTTT | 64326 |
rs371338772 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176073335 | ATGCTTGATACAACT[C/T]CATTCCAACAGTTTG | 64326 |
rs371339841 | snp | C/T | 0.000138872 | 0.00833167 | intron-variant | RFWD2 | GRCh38.p7 | 1:175988460 | TAAAATTTCTTGGCA[C/T]GAAACTCATCACTAC | 64326 |
rs371383311 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175985801 | GTTGGTCCAAATTAC[C/G]TAGTCTGTCAATTAG | 64326 |
rs371387972 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176149757 | AACACAAGTATGTAT[A/C]ATTTACTGTTAAAAT | 64326 |
rs371395122 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176087622 | AGGTGCTGGAGAGGA[C/T]GTGAAGAAACAGGAA | 64326 |
rs371397392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176149333 | GAAAAATCTTTTCAC[A/G]GATAATGGCAATTCT | 64326 |
rs371398318 | snp | C/T | 0.000256782 | 0.0113281 | intron-variant | RFWD2 | GRCh38.p7 | 1:175945218 | AAATCATTTAAGATA[C/T]AAAAGGAATTTAATG | 64326 |
rs371402519 | snp | C/T | 0.000153988 | 0.00877327 | intron-variant | RFWD2 | GRCh38.p7 | 1:176163936 | CATAATTTGTATTTT[C/T]GTTAAATGTATCATG | 64326 |
rs371403289 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176064096 | ACCATCTGTACCTGA[C/T]GGATCTTTCAAAACT | 64326 |
rs371404052 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176160503 | ACAGAATGGGGAAAA[-/A]TTTTTGCAATGTACC | 64326 |
rs371471550 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176001766 | AGAACTCTCTCTGGT[A/G]TTTCTTATGGGGTAG | 64326 |
rs371507725 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176202469 | GCTGGGATTACAGGC[A/G]TGAACCAAGGTGCCC | 64326 |
rs371510440 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176136302 | AAACAAATTTAGACT[A/G]TATTTTATCAAGTGT | 64326 |
rs371521509 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176196497 | ATAAATTCAGCAACA[C/T]GGGTGTAATGGAGAA | 64326 |
rs371532118 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176204447 | GACCCACAGCCAAAC[A/G]GGGGGAAAAAAAAAG | 64326 |
rs371534954 | in-del | -/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175965583 | TTTTTTTTTTGTTTT[-/G]TTTTTGTTTGTTTGT | 64326 |
rs371545851 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176008206 | CCTGCATCAGCTCGC[A/G]CACGGTGCACGCACC | 64326 |
rs371565463 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176003449 | GTCCTGAATGGTATT[G/T]CCTAGGTTTTCTTCT | 64326 |
rs371577511 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175993762 | AAAGACCAAATCTAC[A/G]TCTGATTGGTGTACC | 64326 |
rs371577630 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176060772 | AGAATATTTCATCAT[A/G]TATATTTAAAAATGT | 64326 |
rs371586906 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176004289 | ATATACAATCATGTC[A/G]TCTGCAAACAGGGAC | 64326 |
rs371587986 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176063398 | GTCATTAACACAACT[A/C]TCAAAATTCAAACTT | 64326 |
rs371590395 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175951357 | ATTTATTCATAGAGA[C/T]AGATGTAACTGATTT | 64326 |
rs371594704 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176070626 | AAGACCGCACCACTG[C/T]ACTCCAGCCTGAGCA | 64326 |
rs371594841 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175991511 | TTAACAGTATACCTA[C/G]GCTACACTAAATTTA | 64326 |
rs371622833 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176124880 | CTAAATTACATTCCC[A/T]CCAGCACCATACAAG | 64326 |
rs371627965 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176088595 | GAAGGCATAATAAAA[A/G]ATTATTTTATTATTA | 64326 |
rs371702745 | in-del | -/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176189389 | ATTATGTTTCTTTTT[-/T]CCGTTGGGAATTCTT | 64326 |
rs371716051 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176036932 | TAAATCTTGTAACAA[A/G]TAAAATGTATCGATT | 64326 |
rs371717613 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175977499 | TCCTGGAAATAGCTG[A/G]TGTCAACCCTGATAG | 64326 |
rs371725157 | in-del | -/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176204169 | CTGAGTTCTCATTTT[-/T]GTCCTTACCTGTCCA | 64326 |
rs371748359 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176051741 | AGTGATTCTGTTGAC[C/T]GTGACCGTATGTAGG | 64326 |
rs371749663 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176007984 | CAGACTGCTCTGCTA[A/G]CAATCAGGGAGACTC | 64326 |
rs371760056 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176007803 | TGTCTTTTTGTTTGT[C/G]TGTGCCCTGTCCCCA | 64326 |
rs371763332 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176138323 | AAAGAGATGGGCAAA[C/G]GAAGAAGCAGCATTA | 64326 |
rs371765725 | in-del | -/CA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176105751 | TTTTGGCGCAAAACA[-/CA]TCAGTTGGTCAGCAT | 64326 |
rs371770591 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176026209 | GATAATATTCATATC[C/T]GGCATTGGTACAAAT | 64326 |
rs371770718 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175970126 | TTGAAGCAAGGAATG[G/T]ACCTGGGGCAACACT | 64326 |
rs371773395 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176186847 | ATTCTGAAGGTAGGA[A/C]TATGGTTTGCTGATA | 64326 |
rs371791998 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176171168 | GCTGTTATATCTACA[C/T]TGAAAATCTGTCATT | 64326 |
rs371827387 | snp | A/G | 3.77665e-05 | 0.00434532 | intron-variant | RFWD2 | GRCh38.p7 | 1:176163797 | TTATTAAAAATAGTA[A/G]TAAGAGTTGAAACAT | 64326 |
rs371838669 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175996399 | GAAGTTCTGGCCAGG[A/G]CAATTAGGCAGGAGA | 64326 |
rs371839739 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175996503 | TCTAGAAAACCCCAT[C/T]GTCTCAGCCCAAAAT | 64326 |
rs371849503 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176083707 | GTTGGAAATAAAAGA[G/T]AATACAGATGGATTT | 64326 |
rs371854942 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176004580 | TTGTTGCATTTTGTT[A/G]AAGGCTTTTTCTGCA | 64326 |
rs371883151 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176021540 | ATGACTAATAAATAC[A/G]GGACATAATTTTTTA | 64326 |
rs371884487 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176120816 | AAGATAATAGGCATA[C/T]TGATTTTAGACTAGC | 64326 |
rs371893811 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176144767 | AGGTGAAACTTCAGA[G/T]TGATGAAGAAAGAAT | 64326 |
rs371902170 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176150440 | TGACTGGACCTTAGA[A/C]CCATTCTTCCCAAGT | 64326 |
rs371941501 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176020671 | ATCAGAGCAAGACTC[A/T]GTCCCAACAACAACA | 64326 |
rs371943582 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176119996 | CCACAAGAACGACCA[C/T]GCTATATAAACTACC | 64326 |
rs371943751 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176101457 | GTCCTCTCTTCACTG[A/G]TAAGTAATCGTGTCT | 64326 |
rs371961550 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992422 | TGCAGCGCACCGTGC[A/G]CGAGCCAAAGCAGGG | 64326 |
rs371964246 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176099999 | CCTATGTAAAAATAA[C/T]TAATCTTGCTGCACT | 64326 |
rs371966942 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175997738 | GGCAATCATTAAAAA[C/G]TCAGGAAACAACAGG | 64326 |
rs371970215 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176109449 | TTACTTTTTGGTAGA[C/T]TTTAAATTTTTATTC | 64326 |
rs371973824 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176035191 | AATTATACTCCATGG[A/G]GTAAAAATAAACAAA | 64326 |
rs371974392 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175951902 | GACTAAAATGTTTCA[A/G]ATTTGTAAACTATAA | 64326 |
rs371984114 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176110226 | TGCAAAGTATATAGG[G/T]AGACAAGTACCTATT | 64326 |
rs371999989 | snp | A/T | 3.35751e-05 | 0.00409712 | intron-variant | RFWD2 | GRCh38.p7 | 1:176148978 | AATAGTAAATAAAAC[A/T]TTATGTAAAACACAC | 64326 |
rs372001282 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176065542 | TGCCACCCCAAAATA[C/T]GTCACTCTGCCATAA | 64326 |
rs372032611 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | RFWD2 | GRCh38.p7 | 1:176069297 | CAGCATCCTATCTTT[A/G]AAATCAAGCACAGAA | 64326 |
rs372059805 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176187002 | GCAGGGGTACAGTAC[A/G]TGTCATGTCACATAA | 64326 |
rs372060922 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175982958 | AAGTTTTTGAGATGT[A/G]TTGCATAGCAGAGTG | 64326 |
rs372078802 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175992053 | TGTAGTATACGTAAT[C/T]GTATGTGCTAGACTT | 64326 |
rs372094495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176125565 | GTTTCGGGGTCCTCT[A/G]TTCGGTTCCATTGGC | 64326 |
rs372104208 | snp | G/T | | | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207595 | GGGTCACCCAGGGTA[G/T]CCGCCCCAAGCGGAG | 64326 |
rs372119482 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176094482 | CTTCAAATAAAACAA[A/T]TTCAAGATAAGCTCT | 64326 |
rs372126228 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175954249 | AATAAAAATGCAACA[C/T]ATCAAAATTTGTGTA | 64326 |
rs372133832 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176053859 | TCTGTTACCATTTTC[A/G]TTCTCTTATTTTTTG | 64326 |
rs372145889 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176073120 | ATCTCAGTTTTTTTC[A/T]TCTGTAAAATGAGGT | 64326 |
rs372150925 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176007853 | CAGGCAGGCCTCCTT[C/G]AGCTGTGGTGGGCTC | 64326 |
rs372187029 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176029418 | TACAAAGGTACCAGA[G/T]CAACTATCATATCAT | 64326 |
rs372220393 | in-del | -/GT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176165362 | AGAGAGATGTGTGTC[-/GT]GTGTGTGTGTGTGTG | 64326 |
rs372243920 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176192166 | GTATCTCTGCTGATT[C/T]CTCTTACCCCAATAC | 64326 |
rs372272610 | in-del | -/TTCAA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176195591 | ACGAGTCTCTATAAA[-/TTCAA]AAGGACTAATATCAT | 64326 |
rs372284795 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176083702 | TAATAGTTGGAAATA[A/T]AAGAGAATACAGATG | 64326 |
rs372315811 | in-del | -/GCC | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176139997 | TCTGTAATATCAATA[-/GCC]AAAGACAGCCAATAT | 64326 |
rs372316536 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176039858 | AAAATGAAATATCCA[-/C]AGATAAAAGAATAAA | 64326 |
rs372322247 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176100155 | AGCACTTTGGGAGGC[A/C]GAGGCAGGTGTATCA | 64326 |
rs372346623 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176001989 | TAATGAGGATCCCTG[A/G]TACTTGCTGAGCAAC | 64326 |
rs372359216 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176017387 | AGCTTTTGGATACTG[C/T]GACAGGACTGGGGTG | 64326 |
rs372372343 | snp | A/T | 0.000153988 | 0.00877328 | intron-variant | RFWD2 | GRCh38.p7 | 1:175989338 | TCTGTATTAAGCTCA[A/T]CCTCTGAGGAGAGTA | 64326 |
rs372381333 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175996594 | TCACAAGCATTCTTA[C/T]ACACCAATAACAGAC | 64326 |
rs372389207 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176060236 | AAACAAATAAATACA[C/T]TACCTGATAGACTAT | 64326 |
rs372413357 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | RFWD2 | GRCh38.p7 | 1:176003275 | AGATGAGTAGGTTGC[A/G]AAAATTTTCTCCCAT | 64326 |
rs372425386 | snp | A/C/G | 4.96576e-05 | 0.00498265 | intron-variant | RFWD2 | GRCh38.p7 | 1:176134991 | GAATTCTAATCAATT[A/C/G]CAAGTGTGAAGCTTG | 64326 |
rs372443736 | snp | C/T | 3.36219e-05 | 0.00409998 | intron-variant | RFWD2 | GRCh38.p7 | 1:176046132 | TGATAATTACATATG[C/T]AAATTGTTACATCTA | 64326 |
rs372490136 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176165565 | CCTGACATGGTGGCA[C/G]GTGCCTGTAGTCTCA | 64326 |
rs372498777 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176147924 | TCTTTTTTTGGGACA[A/G]ATTCTCGCCCTGTTG | 64326 |
rs372499557 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176125708 | GCTTTGGCTCTTCTG[A/G]GTCTTTCGTGATTCC | 64326 |
rs372509987 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176041422 | GCGAGACCTGGAATC[A/G]CTACAACCTCTGCCT | 64326 |
rs372517280 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176085121 | TCCACATCTTTGCAT[A/G]TGTTATTTCCTCTAC | 64326 |
rs372520018 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175961240 | TGTCATAGATCTAAC[G/T]ATACATGTCCTATTA | 64326 |
rs372522551 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176062282 | GCTGGGATTACAGGC[A/G]TGAGCCACTGAGCCC | 64326 |
rs372536306 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176005704 | TAGTTTGATTGCACT[G/T]TGGTATGAGAGATAG | 64326 |
rs372565924 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176152315 | AGTAAATAAAAACAA[C/T]TAAAAATTGAAAAGA | 64326 |
rs372573979 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175948357 | GGTGGTAAACAGACT[C/T]AAAATGTCATAGAGG | 64326 |
rs372599867 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176157913 | GAACAAAACTATTCA[C/T]CAATGACCTAAAGAA | 64326 |
rs372600821 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175986254 | TTGATCTCCTGACCT[C/T]GTGATTTGCCCGCCT | 64326 |
rs372605130 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176179190 | AGCTACTCAGTAGGC[C/T]GAGGCAGGAAAATTG | 64326 |
rs372608244 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176122802 | TTTTTTTTGTAAGAG[G/T]AGTTTCCTTAGAAAC | 64326 |
rs372625833 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176079944 | ATGAGGACTGCATGA[A/G]CCTAGGAGTCTGAGG | 64326 |
rs372628748 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176003213 | GGGGTTGTTTTCTTG[A/T]AAATTTGTTTGAGTT | 64326 |
rs372632677 | in-del | -/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176188780 | CTGCTATTTCCCCCC[-/T]CTCTTCCTCTCCTCA | 64326 |
rs372633957 | snp | C/G | 0.00124859 | 0.0249547 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176206928 | GGAGGCCGCCGAGGA[C/G]CCGGGGCTTGTCCCA | 64326 |
rs372636068 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175977862 | TACATACACTTCAGC[A/G]TATTACACCAATTCA | 64326 |
rs372659400 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176077546 | CCACAGCCAACTTAA[C/T]AGTGAATGGGCAAAA | 64326 |
rs372692127 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176028118 | ACCTGCTATGATTCA[A/G]TTATCTCCACCTGGC | 64326 |
rs372694045 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176118330 | AAATAAATCATATGA[A/C]TCTGTCTACACAGCA | 64326 |
rs372709887 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176169002 | AAATGCCTGACTTGT[G/T]AATAGGGCATCTAAA | 64326 |
rs372727001 | in-del | -/GGTTTAAA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176047540 | GGCTAAAGGTTTAAA[-/GGTTTAAA]ATCTATGTGTATGAA | 64326 |
rs372756199 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176077924 | CAAAGAAAATAACTA[A/G]GAACTCATCTAAGCA | 64326 |
rs372764339 | snp | C/G | 0.00018146 | 0.0095235 | intron-variant | RFWD2 | GRCh38.p7 | 1:176027533 | TACCATGATATTTAA[C/G]CAACATCAAAGGAAG | 64326 |
rs372783961 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:176007288 | TTTGCCTTTGGTTTG[A/C]ATGTCCTCCCGTAGC | 64326 |
rs372803825 | snp | A/G | | | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207762 | AAGCTGGAGACCCAC[A/G]GAAAGAACCTAGAAG | 64326 |
rs372818735 | snp | A/G | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176075733 | CCTCAGGCTGGGTGC[A/G]GTGGCTCATGCCTGT | 64326 |
rs372834242 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176118413 | AGAAAGAAGTTCTAA[A/G]GTTTGACAGAAGATT | 64326 |
rs372866294 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176204119 | GAAACTCTCTAATTG[C/T]ACACAAAGAAAACAC | 64326 |
rs372877977 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176018380 | TCCCACAATTAAAAA[A/G]AAGTCTCAGTTAAGA | 64326 |
rs372893251 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175950972 | AAAAATCTGGATGGC[A/G]CTGTGGGTCACACCT | 64326 |
rs372898516 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176008948 | CGATTTGTGTGTATG[C/T]TGTGGAATGCTTTCA | 64326 |
rs372899325 | in-del | -/CC | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176040752 | AGACTGTGCTCCATT[-/CC]ATTTCATTTCTTTTA | 64326 |
rs372904962 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176033940 | AATATTTTATATGAT[A/C/G]GCCAAACAGACAAGA | 64326 |
rs372905477 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176199436 | CACTACTAGATATTT[A/T]TACCCTAAAAATGTG | 64326 |
rs372909396 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176058529 | AAGGGCGGTGCAAGA[A/T]GTGCTTTGTTAAACA | 64326 |
rs372913842 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176126549 | GCAACCTCTGCCTCC[C/T]GGGTTCAAGTGATTC | 64326 |
rs372919485 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176139884 | TGGGGTCAATCATAC[C/G]CCAAATTTTAGCATC | 64326 |
rs372926444 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175951163 | CTGAGACAGGAGAAT[C/T]GCCTGAACCCGGGAG | 64326 |
rs372946499 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176183397 | AAAAATAATTAAAAA[-/A]TACACAGATTACACA | 64326 |
rs372975968 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176188860 | ACACACACACACACA[C/G]ACAGAGAACAAAGCA | 64326 |
rs372976651 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176131293 | ATTGCTAGATGAGGT[A/G]ATGCTAAGGATCTAA | 64326 |
rs373003068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176186008 | GATGATATTACAACA[C/T]AATGTGAAAATATAT | 64326 |
rs373015607 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175996824 | AATGGCCATACTGCC[A/C]AAGGTAATTTATAGA | 64326 |
rs373020263 | in-del | -/TTTT | 0.00993419 | 0.0697739 | intron-variant | RFWD2 | GRCh38.p7 | 1:176056798 | CATCTGATTTCTTTC[-/TTTT]GTTTTCTGTGTTATT | 64326 |
rs373028395 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176158921 | GCTAGGGTTACAGGC[A/G]TAAGCCACTGTGCCT | 64326 |
rs373033236 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175972172 | TGGTCCTCACCTTCA[A/G]AAAGTCTAAATATAA | 64326 |
rs373048934 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176096419 | GGTTTGGGTGCATGG[C/T]CATGTCTGCCACATG | 64326 |
rs373062573 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176157710 | TATATAAAGGATTAC[-/A]AAAATATTCAGCACT | 64326 |
rs373068556 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176150674 | GTGACAGTTCATTTA[A/C]AAAGGAATTATACAA | 64326 |
rs373078663 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176025880 | GGTGACCCTGTCTCA[A/T]AAAAACAAAAAAACC | 64326 |
rs373083050 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176083711 | GAAATAAAAGAGAAT[A/G]CAGATGGATTTACAG | 64326 |
rs373086557 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176035789 | TGATCTGACACTTAC[A/G]GAACACTCACCAAAC | 64326 |
rs373105934 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175984121 | TAATCCCCAAGACCA[C/T]GGGGAAAATGTCTCC | 64326 |
rs373114048 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175973713 | TCTACAATGGAAAAA[-/A]GTAAGTCTAGATCAA | 64326 |
rs373115144 | in-del | -/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175976190 | TAATTGGGAAAGGTA[-/T]AACTATTTTATTCTG | 64326 |
rs373120762 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176086586 | TCAAATAGAAAATGA[C/G]TTACTTTTTCCAACG | 64326 |
rs373134757 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176017653 | CCTCAGCCACCCAAG[G/T]AGCTGGGACCACAGG | 64326 |
rs373168755 | in-del | -/AAT | 0.495634 | 0.0465208 | intron-variant | RFWD2 | GRCh38.p7 | 1:176019464 | CAAGACTCCATCTCA[-/AAT]AATAATAATAATAAT | 64326 |
rs373175064 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176111076 | AGAATCACCTGAACC[C/T]GGGAGGCGGAGGTTG | 64326 |
rs373187970 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176036508 | AAAAAACAAAAAAAC[-/A]AAAAAAAAAAAAAAA | 64326 |
rs373227197 | in-del | -/CAA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176189808 | GACCAAAACAAACAA[-/CAA]TCATAATCTAATATT | 64326 |
rs373230661 | in-del | -/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176014887 | ACATTGTGGGGGATA[-/C]AATAATGAACAAGAA | 64326 |
rs373249566 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176137663 | GGTAGGCTTATTGTT[C/T]CAGAATTCATGCTTT | 64326 |
rs373263025 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176069161 | CTGCACTCCAGCCTG[A/T]GCAACAGGGTGAGAC | 64326 |
rs373279693 | snp | A/G | | | synonymous-codon | RFWD2 | GRCh38.p7 | 1:175989424 | TTTACGGTGTCCTTT[A/G]AATACCATGATTGGC | 64326 |
rs373285924 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175996622 | GACAAACAGAGAGCC[A/G]AATCATGAGTGAACT | 64326 |
rs373289657 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175958460 | AAAAGAAAGGTAAAT[A/G]TTTTTGTCATTCCTC | 64326 |
rs373293626 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175972166 | GGTTCTTGGTCCTCA[C/T]CTTCAGAAAGTCTAA | 64326 |
rs373316108 | in-del | -/C | | | frameshift-variant, utr-variant-5-prime, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176206732 | GGACAGGCCCGTGGA[-/C]CACCGCCCCGCCGCC | 64326 |
rs373324066 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176040613 | CCATGCCTGGCTGAC[G/T]AGTTCTTAAATCAAG | 64326 |
rs373330844 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176136575 | TAGAGAGAGAAAGAC[-/A]AAAAAAAAAAAGCCT | 64326 |
rs373330929 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176055199 | ATCACTTCGGGAGGC[C/T]GAGACAGGTGGATAA | 64326 |
rs373342525 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175994047 | TAAGAGGGGATCTCT[G/T]GGCAGAAACTCTACA | 64326 |
rs373349935 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176005562 | TTGTGTCTTTGTTCT[C/T]GTTGTTTTCAAAGAA | 64326 |
rs373352549 | snp | C/G | 1.75477e-05 | 0.00296202 | intron-variant | RFWD2 | GRCh38.p7 | 1:176085741 | CAGATCTGAAATGTA[C/G]ATTTCAGATAATTTG | 64326 |
rs373353213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176042171 | AGCTAAATGGGAGGT[A/G]GAGGCAGGAGAATCA | 64326 |
rs373356966 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176042262 | GGCGACACAGCGAAA[C/T]TCTATCTCAAAAAAA | 64326 |
rs373360912 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176114629 | GTCTCACTCTGTCAC[C/G]CAGGCTGGAGTACAC | 64326 |
rs373372857 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176005825 | AAACATGCATATTCT[A/G]TTGATTTGGGGTGGA | 64326 |
rs373391688 | snp | A/G | | | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176209203 | TGTTTTAAAAAATAT[A/G]TTAGTGACTACCTCC | 64326 |
rs373398205 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176189999 | CAAGAGTAAATAAGC[A/G]TAATGAATAATGATT | 64326 |
rs373406932 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176086657 | CATGGATAGGAAGAA[C/T]CAATATTGTGAAAAT | 64326 |
rs373427286 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176115782 | TAAAAATAAAAAGTC[A/G]AAAAAAGCCTATTAG | 64326 |
rs373450993 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176138424 | TTAAAAGAGTGATTA[C/G]CATTTTCAAAAGCTT | 64326 |
rs373458775 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176013974 | AGTTCATTCCAATAA[A/G]TGCTCTTTTAATTTT | 64326 |
rs373481116 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175957929 | GTGCAAAAAATTACA[C/T]ACTGTATCATTCCTG | 64326 |
rs373495715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175953120 | AATAAAAGGGGAGAA[C/T]AGAAGTATAATGTTA | 64326 |
rs373510613 | snp | A/C/G | 3.49066e-05 | 0.0041776 | intron-variant | RFWD2 | GRCh38.p7 | 1:176175872 | ACAATTTTGGGGATC[A/C/G]AAATATTTTTAAAAT | 64326 |
rs373536136 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176006161 | TTTTATCAGAGACTA[A/G]GATTGCAACCCCTGC | 64326 |
rs373540738 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:175975050 | CTGTCAGTAAGAAAC[A/T]TGGCACCTAAAGGGC | 64326 |
rs373541603 | in-del | -/AAAC | 0.00755907 | 0.0610114 | intron-variant | RFWD2 | GRCh38.p7 | 1:176051588 | ACTTATTTTAAAAAA[-/AAAC]AAACAAACTGTAAAG | 64326 |
rs373544711 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176001204 | TATAAAACTCTTCTT[A/G]GGAGTTATTTCTAAA | 64326 |
rs373547704 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176020626 | AGGCTGCAGTGATCC[A/G]AGACTGTGCCACTGC | 64326 |
rs373556870 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175984590 | GCTGTGAGAAGAGGG[A/C]CACCATCCGCCAGAC | 64326 |
rs373557040 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175995601 | ATACAAACTACCATC[A/G]GAGAATACTACAAAC | 64326 |
rs373562003 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176084264 | ATGAGCCACTGCGCC[C/T]GGACTGATTTTGGGA | 64326 |
rs373562703 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175965538 | TCTTTTGTTTTTGGA[G/T]CTCAGAGAAATTCAT | 64326 |
rs373583303 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176013050 | CATAGTATATGCTTA[G/T]AACTTCCACACCTCC | 64326 |
rs373586253 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175995541 | AAGAATCAAATAGAT[A/G]CAATAAAAAATGATA | 64326 |
rs373597660 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992607 | ATATCCCGCACCTGG[C/T]TCGGAGGGTCCTACG | 64326 |
rs373612176 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | RFWD2 | GRCh38.p7 | 1:176085900 | CTTTGTCTAAAATAA[C/T]AAGAAAAGACACAAA | 64326 |
rs373631748 | in-del | -/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176139788 | GATGGTTACAACAGA[-/C]ACAGGGAACTACTGG | 64326 |
rs373632224 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175951022 | AGGCCAAGGCAGGCG[A/G]ATCACCTGAGGTCGG | 64326 |
rs373669256 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176006416 | CTGGTTATTTTGCTC[A/G]TTAGTTGATGCAGTT | 64326 |
rs373671741 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175964364 | CAAAAATCAGAAATG[C/T]TTTCTCCCCTAAAAC | 64326 |
rs373672925 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175982023 | AAAAAGATGAAAGAT[A/T]ACAAGCGTTGGCAAG | 64326 |
rs373673220 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175959499 | ATAAGTACTGGAAAA[A/G]CAGACACTAAACTTT | 64326 |
rs373677030 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176070514 | TAAAAATACAAAAAT[C/T]AGCTGGCTGTGGTGG | 64326 |
rs373732728 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175976270 | TATCAATTAGTCATT[C/T]TTTTTTTTTTTTTTT | 64326 |
rs373767946 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176093916 | TAGTCCCAGCTACTC[A/G]GGAGGCTCAGGCAGG | 64326 |
rs373775436 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176173768 | TGAGGCGGGAGGATC[A/G]CTTGAGTCCAGGAGT | 64326 |
rs373787922 | in-del | -/AT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175985979 | AGCTATTTTAAAAAT[-/AT]GATACTAATAACTCA | 64326 |
rs373790483 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176007610 | ACCCTGCCGTGTGAG[A/G]TGTCAGTGTGCCCCT | 64326 |
rs373790941 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176095281 | TACAGAATTTAGAAT[A/G]GTGGTTATCATAGTG | 64326 |
rs373796817 | in-del | -/TA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176072783 | ACTATCATAGAAACA[-/TA]AAGTTTAATTTGAAT | 64326 |
rs373802739 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176061624 | AGAGTGAAACTCCGT[C/T]TCAAAATAAAAAAAA | 64326 |
rs373812172 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176008321 | GCGTTGCTCATGCTG[C/G]GAGCTGTAGACCGGA | 64326 |
rs373816729 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176183272 | TCATATCCAACTTCA[C/G]CATAAAATTACGGGC | 64326 |
rs373823470 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176122680 | TAACAGTTACATAAT[A/G]CATACAGGGACTATG | 64326 |
rs373869937 | in-del | -/A | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:175965577 | AAACAAAAACAAAAC[-/A]AAAAAAAAAACCCAG | 64326 |
rs373879799 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176182871 | ATAAAAAGTATTCAA[C/G]AAAGTAAAATGACTT | 64326 |
rs373899859 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176100118 | GGACTGGCAGGGTGC[A/G]GTGGCTCACGCCTGT | 64326 |
rs373907202 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176036074 | ATGGAAAAGCAAATA[A/C/T]ACTAGTCATGAAAAT | 64326 |
rs373911733 | snp | A/C/T | 0.00915205 | 0.0671238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175993406 | GGAGAATGGCTTTGA[A/C/T]GAGTTGAGAGAAGAA | 64326 |
rs373927362 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176004910 | TTCTATTGATTGGAA[C/T]AGTTTCAGAAGGAAT | 64326 |
rs373928991 | snp | A/G | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176186556 | AAAAGAAAAGAGAAA[A/G]AAAAGGGCACCTCAA | 64326 |
rs373930147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175954838 | CTTAACAAAATACAA[A/G]TAAAGATAATTCAGT | 64326 |
rs373942040 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176121525 | TCGTTTTTTATTTTT[A/T]TGTTTTTAGAGGTAC | 64326 |
rs373990377 | in-del | -/ATT | 0.00795532 | 0.062565 | intron-variant | RFWD2 | GRCh38.p7 | 1:175999151 | AAAATGTACAATTAA[-/ATT]ATTATTGACTATAGT | 64326 |
rs374006815 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175982676 | GTGGAGGGTCAGTGC[C/T]TCTTGCCCCCACGTT | 64326 |
rs374029898 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176065978 | TCAAACACCTGCCTC[A/G]GCCTCCCAAAGTTCT | 64326 |
rs374040184 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176128471 | TCAAGTTCAACTCCT[C/T]GGCATGGTTTAGGGT | 64326 |
rs374052454 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176184077 | TAAAATTATAAATTC[C/T]TCCAAGACTAAAGAA | 64326 |
rs374053160 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176035741 | AAAAAAACGCAAGCA[C/T]ACAGAAAATCAGAAA | 64326 |
rs374068029 | in-del | -/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175999966 | TTATTAGATTTTTTT[-/T]CCCTACAAAATTGTC | 64326 |
rs374086825 | snp | G/T | 0.000318859 | 0.0126225 | intron-variant | RFWD2 | GRCh38.p7 | 1:176043870 | AATAAATAACAATGG[G/T]ATAAAAATAATTTTA | 64326 |
rs374099230 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176204841 | GCTGAGGCTGGAGAA[C/T]TGCTTGAACCCGGGA | 64326 |
rs374100166 | snp | C/T | 1.65225e-05 | 0.00287419 | intron-variant | RFWD2 | GRCh38.p7 | 1:176116578 | ATTTTATAACTCAGA[C/T]AATTATACTCATGGT | 64326 |
rs374102687 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175952233 | TTGAGAGCAGCCTGG[A/C]CAACATGGTGAAACC | 64326 |
rs374106628 | snp | C/T | 0.000347939 | 0.0131852 | intron-variant, nc-transcript-variant, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175968441 | GCCAGCTGTCCTAAG[C/T]CAGACAGAGACCTCC | 64326 |
rs374109713 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175975772 | AAAAGGAAACACAAG[C/T]ATGTAAAAACATGAA | 64326 |
rs374130301 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | RFWD2 | GRCh38.p7 | 1:175972557 | GCAACTGCCACCTCC[C/T]GGGTTCAAGCGATTC | 64326 |
rs374134292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176078275 | ATAACCAAAACAGTA[C/T]GGCACTGGTAGGTAC | 64326 |
rs374140336 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176007344 | CTTCTTCTCTCAGCT[C/T]GTCAAAGTCATTCTC | 64326 |
rs374164603 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176123626 | ATTTTTAACTTTTCC[A/G]GCCCTCTCAAGCCCA | 64326 |
rs374175087 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176072740 | TGCTGCAATTATAAA[C/T]TGAAACTTAGCAAAA | 64326 |
rs374192901 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | RFWD2 | GRCh38.p7 | 1:176161751 | AGTAGATGCTAATAG[C/T]AAACTATGGTTAAAA | 64326 |
rs374198931 | in-del | -/AA | 0.00914312 | 0.0669923 | intron-variant | RFWD2 | GRCh38.p7 | 1:175994634 | AAACCAACAAAGATC[-/AA]AACAGACAAAGAAGG | 64326 |
rs374212539 | snp | C/T | 7.33254e-05 | 0.00605453 | intron-variant | RFWD2 | GRCh38.p7 | 1:176135136 | TTCAAATAGAAGATA[C/T]ATAAATCAAAAAGAG | 64326 |
rs374217706 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176189235 | GAGCAGGCACTGTCT[A/C]ATTGAGAATTTTTTC | 64326 |
rs374221902 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | RFWD2 | GRCh38.p7 | 1:176141230 | AGCAAGGCTAGGTGC[A/G]GTGGCTCACGCCTGT | 64326 |
rs374224199 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175983557 | GGACTAATACAGAAA[-/A]TTGGTACCAGAAGTG | 64326 |
rs374231762 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176063047 | AAAATTTTTGAAAAT[G/T]TTTTTTTTTTTTTTT | 64326 |
rs374234996 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176074363 | AATCAACAGAGCTGT[A/G]AGAGTTTTTCACACC | 64326 |
rs374254423 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176007813 | TTTGTGTGTGCCCTG[C/T]CCCCAGAGGTGGAGC | 64326 |
rs374265802 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176026402 | TTTTCCATAATCCTC[A/G]TAACAGCCCCAAACA | 64326 |
rs374285195 | snp | A/G | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176177362 | ATTAAAAAAAAAAAA[A/G]AAAAAAGAAAAAAAT | 64326 |
rs374292631 | in-del | -/GTTAT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176048687 | AAGTGAACTAGTTAT[-/GTTAT]CACTAAATACTTTTT | 64326 |
rs374304505 | in-del | -/AAC | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176076085 | AGGCAGAACACTAAC[-/AAC]GAAATTCTGGACTTA | 64326 |
rs374305639 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176036510 | AAAACAAAAAAACAA[A/C]AAAAAAAAAAAAAAA | 64326 |
rs374310847 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175974540 | TTCAAATGTTAAAAC[G/T]GTATGAAATAAAATA | 64326 |
rs374315300 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176020289 | GCCCTCCAGCCTGGG[C/T]GACAAAGTGAGACTC | 64326 |
rs374325496 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175997679 | GCTATCAGAGAAATG[C/T]AAATCAAAACCACAA | 64326 |
rs374333379 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:175973149 | GCCTTATTTTTTTAA[A/C]ACTTTTACAAGTCTA | 64326 |
rs374342801 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175990853 | TACTTTAACCTATTT[G/T]TGTCTGTGAATCTAA | 64326 |
rs374344855 | snp | C/G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176037385 | TCACTCCAGCCTGGG[C/G/T]GACAGAGCAAGACTC | 64326 |
rs374345499 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176040756 | CTGTGCTCCATTATT[C/T]CATTTCTTTTATGTA | 64326 |
rs374362432 | snp | C/T | 0.000253115 | 0.0112469 | utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175945135 | AGGATCAAGTACAAT[C/T]TGACTTGAGTTAACC | 64326 |
rs374362996 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176056095 | AAGCTATTAAATTTC[C/T]GTGTGGTATATTTTT | 64326 |
rs374370495 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:176097890 | AAAAAAAAAAAAAGC[C/T]CTAATTAATTGGCCT | 64326 |
rs374406944 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176127850 | AGCTGTACTATTTAC[A/G]ATACCACCAACAGTT | 64326 |
rs374411905 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176099739 | CAGAGCCAATAAAAG[C/G]CCCTTGGGAAAAATG | 64326 |
rs374424197 | snp | C/T | 3.31411e-05 | 0.00407056 | intron-variant | RFWD2 | GRCh38.p7 | 1:176134959 | AAGGACTAGACCATA[C/T]GCATACTTTGTAATA | 64326 |
rs374427359 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176143653 | ATAACGGCCAAGTTT[C/G]GTTTATATAAGGGGT | 64326 |
rs374430179 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176120799 | AATGGTTCACTCTTG[C/G]AAAGATAATAGGCAT | 64326 |
rs374472529 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176025808 | GGTTGGAGGATCACT[G/T]GAGCCAGGGAGGACC | 64326 |
rs374518525 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176112909 | TTCATTCTTTTTTAC[A/G]GCTGAATAATATTCC | 64326 |
rs374547061 | snp | C/G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176203571 | CTAGTTAAATGAACC[C/G/T]TAAGAAAATTTTGCA | 64326 |
rs374574794 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175991275 | TGTGCTCCTATGCTA[A/C]AAACCTATGTATCAT | 64326 |
rs374612230 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176025088 | AGAAAAAGCATAAGC[A/G]CCAATTGGTGCTAAA | 64326 |
rs374614941 | snp | A/G | 1.69155e-05 | 0.00290817 | utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175945110 | TTGTCAGCTGCAGAT[A/G]TATTTCAGCAGGATC | 64326 |
rs374618417 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176001939 | GGCAGTAATGATTTC[C/T]GACGAGAAGTCATCA | 64326 |
rs374642143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176021922 | AGATTCCATCTTCTA[C/T]ATACATACTTGTTAA | 64326 |
rs374656418 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176166621 | GTTACTTGAAAAAAT[G/T]GTTATTTTTTTCTTC | 64326 |
rs374665646 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176130358 | TGCTTGCCTACCAAT[C/T]TCTAATTTTCTCATT | 64326 |
rs374670176 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176178129 | CACTGAAGGAAATAA[C/T]ATACTAAATCTTTAT | 64326 |
rs374670738 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176179271 | CTCCAGCCTGGGCGA[C/T]AAAGTGAGACTCCGT | 64326 |
rs374676555 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176204572 | TCATTAATTAATTCT[C/T]CTGAATATTAAACCT | 64326 |
rs374680107 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176110634 | CCTAGTAAATATGAG[G/T]TATGTTTAAAACAAA | 64326 |
rs374681072 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176155435 | AACACAGTTCAATAC[A/G]AATTATTTAAATTCA | 64326 |
rs374691370 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176132238 | CTAAATCAGATCCTG[C/T]TCAACACTATCCCAT | 64326 |
rs374693365 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176064270 | ATTGCCAAAAAATTT[C/G]TCATATTTCATTTAC | 64326 |
rs374700137 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176109233 | TTGTTTGTGGTGCTT[C/T]CTTATATGTAGGGTA | 64326 |
rs374743115 | snp | G/T | 0.00398564 | 0.0444627 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176208787 | TTTTTTGTGTAAGAT[G/T]GTGGCTTTTGGCCAG | 64326 |
rs374747203 | multinucleotide-polymorphism | AA/CC | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176205339 | CAGATTAATTCTGAT[AA/CC]AGAATAACGTACAAA | 64326 |
rs374790338 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176007260 | CTAAATTTTTTTCAA[A/T]GTTTTCAACTTCTTT | 64326 |
rs374792431 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175994659 | AAGAAGGCCATTACA[C/T]AATGGTAAAGAAATC | 64326 |
rs374810476 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176039807 | GCCAGACCATTCAAT[-/A]GGGAAAGGACAGTTT | 64326 |
rs374830292 | snp | C/T | 1.6517e-05 | 0.00287372 | missense | RFWD2 | GRCh38.p7 | 1:175987014 | CTTTTCGGTCTTTGT[C/T]GAGAACACTTTTGAC | 64326 |
rs374832890 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176088718 | AATATCTATTTGGCC[C/G]GGCGCAGTGGCTCGT | 64326 |
rs374871944 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176108856 | CGGTGGCTCATGCCT[C/G]TAATCCCAGCACTTT | 64326 |
rs374909267 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175952239 | GCAGCCTGGCCAACA[A/C/T]GGTGAAACCCCATCT | 64326 |
rs374914875 | in-del | AA/G | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176176820 | CTGAAAAAAAGAGAA[AA/G]AAAAGACAAAAGAAA | 64326 |
rs374923042 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176205242 | ATCGACTGTGTAGAA[C/G]TGCAAACACTTCTCA | 64326 |
rs374926984 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:176017549 | TATTTTTTTGAGACA[A/G]AGTCTTGCTCTGTCA | 64326 |
rs374934844 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175985978 | AAGCTATTTTAAAAA[A/T]ATGATACTAATAACT | 64326 |
rs374942511 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176002186 | TTTCTACCTCTTTCT[C/T]TCTCCTCATCTTTTG | 64326 |
rs374948295 | in-del | -/A | 0.0966517 | 0.197444 | intron-variant | RFWD2 | GRCh38.p7 | 1:175956233 | ACAACTTGGCAAGTT[-/A]AAAAAAAAATAGAGT | 64326 |
rs374949962 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176099964 | TTGTGGAAGAGTTCC[A/C/G]TCCAAGCCAATCTAA | 64326 |
rs374951000 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992290 | GCCAAATAGGAACAG[A/C]TCCAGTCTACAGCTC | 64326 |
rs374953663 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175997776 | GAGGATGTGGAGAAA[C/T]AGGAACACTTTTACA | 64326 |
rs374968100 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176078290 | TGGCACTGGTAGGTA[A/C]AAAAACAGACATAAG | 64326 |
rs374990612 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176125001 | TGTAGTTGTGATTTG[A/C]ATTTCTGATGATCAA | 64326 |
rs374991027 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176204446 | GACCCACAGCCAAAC[-/A]GGGGGGAAAAAAAAA | 64326 |
rs374994751 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176149998 | TGCCTGGCTATGCAA[C/G]AGAATTACCTGGGGC | 64326 |
rs375010287 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176158895 | ATCCACCCACCTCGG[C/G]CTCCCAAAGTGCTAG | 64326 |
rs375021097 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176104922 | GTGATTAAGTAAATT[A/C]CAGTACAACCACATG | 64326 |
rs375033166 | in-del | -/AA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175988842 | TGTGCCAAAAAAAAA[-/AA]GTTTTCTTTTCAACA | 64326 |
rs375046950 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175996473 | GTCCCTGTTTGCAGA[C/T]GACATGATTGTATAT | 64326 |
rs375065354 | snp | A/G | 1.73634e-05 | 0.00294642 | missense, utr-variant-5-prime | RFWD2 | GRCh38.p7 | 1:176206627 | GCCCGTTGCAGAGGG[A/G]GGCGAGGAGAGGTCG | 64326 |
rs375077477 | snp | G/T | 1.76135e-05 | 0.00296757 | intron-variant | RFWD2 | GRCh38.p7 | 1:176163806 | ATAGTAATAAGAGTT[G/T]AAACATACGGTGCTA | 64326 |
rs375091153 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176135496 | TAAGATAACTGGATC[A/G]TCAGGTTCAACTCTT | 64326 |
rs375101291 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176054376 | CATGTTGGCCAGACT[G/T]GTTTCAAACTCCTGA | 64326 |
rs375115733 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176119462 | AAATACTCATCAGTT[C/T]GTTGAAGATAAAACT | 64326 |
rs375128378 | in-del | -/AAAT | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176062745 | CAGACAAGTTTATTC[-/AAAT]AAATAAACTGTACAA | 64326 |
rs375145021 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175988642 | GTTCGAGACCAGCCT[A/G]GCCAACATAGCAAAA | 64326 |
rs375152465 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176175453 | TGTTCCACCTCAGAT[G/T]ATCAGGCATCAGATT | 64326 |
rs375154329 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175947366 | AATCTAATATGAAGA[C/T]ACAATTTTTTTTTTT | 64326 |
rs375157865 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant, missense, utr-variant-5-prime | RFWD2 | GRCh38.p7 | 1:176136490 | CTTGATTCCTTACTT[C/T]CACTCTCTTAATATC | 64326 |
rs375158270 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175993619 | CCTCAGGAGCCGATG[A/C]GATGAACTGGAAGAA | 64326 |
rs375171382 | in-del | -/GTGTGTGT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176165362 | AGAGAGATGTGTGTC[-/GTGTGTGT]GTGTGTGTGTGTGTG | 64326 |
rs375172601 | in-del | -/T | | | intron-variant, utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175967885 | TTTTTCTTTTTTTTT[-/T]GAGATGGAGTCTCGC | 64326 |
rs375173080 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176017368 | TAAAAGTCCTCAATG[C/T]CCTAGCTTTTGGATA | 64326 |
rs375203204 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176155678 | CATGAAACCCAAGAA[G/T]AATAAATATAAAAAT | 64326 |
rs375230382 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176022343 | TCAAACTATAATTGG[C/T]GGGTAGCTCATATAC | 64326 |
rs375233811 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176007215 | CCTTTAAGCACTTCT[C/G]TATATTGGTTATTCT | 64326 |
rs375240115 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176190624 | TCATCTCAGTTAATC[A/T]AGGGTCATATTGCAA | 64326 |
rs375251841 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176040121 | TCAAAATGAAAACAA[C/T]TTTGTGCATTAAAGA | 64326 |
rs375256995 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176028883 | CCCACTCAGCCTCCC[A/G]GGTAGCTAGGTGTGT | 64326 |
rs375266194 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176045918 | AACAACCATGTCCAA[C/G]AAAGACCTTTATTTG | 64326 |
rs375272502 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176066841 | TTTCTCTATTAATGT[C/T]CAGCACTAAGACAAG | 64326 |
rs375283072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176033703 | TTAACATGTAATTAC[A/G]TGCATATATACTTGG | 64326 |
rs375294623 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176077918 | AGCCACAAAGAAAAT[-/A]AACTAGGAACTCATC | 64326 |
rs375320560 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176021279 | AGAAATATAAAATCC[A/G]GCATGCCCACACCAG | 64326 |
rs375326892 | snp | C/G/T | 0.0364509 | 0.129988 | intron-variant | RFWD2 | GRCh38.p7 | 1:176004630 | GGTTTTTGTCTTTGG[C/G/T]TCTGTTTATATGCTG | 64326 |
rs375338059 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176086227 | ATTTTGGGAATCTTT[C/T]TTTTTTTTTTTTTTT | 64326 |
rs375344658 | in-del | -/CCGTTCTCCAACCTATC | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176184299 | GTTCTCCAACCTATC[-/CCGTTCTCCAACCTATC]CCCACAAGTGAGTAA | 64326 |
rs375364310 | snp | C/T | 0 | 0 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207636 | CAAGCGCGGAGTAGC[C/T]GTGTCACGCATGCGT | 64326 |
rs375378507 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176084655 | TTAATTTCAAACAAA[A/C]AAACAAATTTTGCCT | 64326 |
rs375381590 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176136886 | TTAGTTGTTAAACAG[A/G]AAAATTCAGCATGTC | 64326 |
rs375393543 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175972625 | GCCCACGGCCATGCC[C/T]GGCTAATTTTTGTAT | 64326 |
rs375396656 | in-del | -/GTTT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176106041 | TTTTTGTTTTGTTTT[-/GTTT]TTTTGAGACAGAGTC | 64326 |
rs375397207 | snp | G/T | 1.73652e-05 | 0.00294657 | intron-variant | RFWD2 | GRCh38.p7 | 1:176206534 | AGCGGCAGAAACTCA[G/T]AATTTAGGGACAAGG | 64326 |
rs375435561 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176040056 | TTCTTGGATATGACA[C/T]CAAAGGCACAGACAA | 64326 |
rs375435970 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175950350 | GTATGATTACAAAAA[A/G]AGTTATTTAGAATTA | 64326 |
rs375437426 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176005509 | TATAAATTTCCCTCT[A/G]CACACTGCTTTGAAT | 64326 |
rs375448657 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176014740 | CAAAAACCAATGTGT[G/T]TGTATGTATACATAC | 64326 |
rs375455030 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176163418 | TATAGACAAAGTCTC[A/G]CTATGTTGCCCAAGC | 64326 |
rs375468853 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175996649 | AACTCCCATTCACAA[C/T]TGCTTCAAAGAGAAT | 64326 |
rs375473758 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176170908 | AGACTGGTGGATCAC[A/G]AGGTCAGGAGATCAA | 64326 |
rs375475898 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176005640 | GGAGCAGGTTGTTCA[A/G]TTTCCATGAAGTTGA | 64326 |
rs375484608 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176093090 | GTTTTGGCTGTATTT[G/T]AACTTTATAAAAATA | 64326 |
rs375512733 | snp | G/T | 0.0729998 | 0.176553 | intron-variant | RFWD2 | GRCh38.p7 | 1:176168076 | GATTTTTTTTTTTTT[G/T]AAACAGAGTCTCGCC | 64326 |
rs375541033 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176007420 | AGGAAGAGAGGCACT[C/G]TGGTTTTTAGAGTTT | 64326 |
rs375542042 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176091574 | AAGAAAGTGAAAAAA[-/A]GTTGCATTCTGGAGC | 64326 |
rs375546130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175956264 | AATTTTTACAAATGC[C/T]GTTGAAACAACTGCA | 64326 |
rs375548109 | in-del | -/ACACACACAA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175966307 | CACACACACACACAC[-/ACACACACAA]ACACTTAAAAACCTG | 64326 |
rs375563412 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176111141 | TGGACAACAGAGCGA[A/G]ACCTTGTCTCAAAAA | 64326 |
rs375572314 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176014121 | TTCATTTGCAGAAAG[C/T]ATGCAGAATTTGATT | 64326 |
rs375579962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176124803 | CAGTGGGATTGCTGC[A/G]TAATATGCTATTATT | 64326 |
rs375586582 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176004850 | CGGCTTTGGTGTCAG[A/C]ATGATGCTGGCCTCA | 64326 |
rs375614998 | snp | A/C | 6.60709e-05 | 0.00574727 | intron-variant | RFWD2 | GRCh38.p7 | 1:175947251 | ACTCCTAGAAAAGAA[A/C]AAGAGCTTTTAAAGT | 64326 |
rs375642145 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176121858 | ATATAGTGTGGCCTT[-/A]AAAAAAAAAAGTTTG | 64326 |
rs375648170 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175954505 | TCAATAAAATTGATA[C/T]GCCTTAACAAAAAGA | 64326 |
rs375658171 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | RFWD2 | GRCh38.p7 | 1:176057589 | TGATCCGCCAGCCTC[A/G]GCCTCCCGAGGTGCC | 64326 |
rs375677421 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176102335 | TAATCTTTCCCATTC[A/G]TGTGACAAGAGCCCA | 64326 |
rs375677562 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176130996 | CACCCTAGGACCCTA[C/T]AGGTTTGGGGTCTTT | 64326 |
rs375680707 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176006932 | TCTACTGGATAATAT[C/G]CTGCAGAGTGTTTTC | 64326 |
rs375688154 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176135206 | CCCTGTTTGTCTCAA[C/T]ATCAAATTTCTGAAG | 64326 |
rs375694986 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176199102 | GCGTGGGGACCATGA[A/G]GTCCAGGGATCGAGA | 64326 |
rs375703570 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176173071 | TAATCCCAGTACTTC[A/G]GGAGGCCGAGGTGGG | 64326 |
rs375704906 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176100303 | GTGAGGCAGGAGAAT[C/T]GCTTGTACCTGGGAG | 64326 |
rs375706150 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176198437 | AGCCTTCAACCCTTA[C/G]CAAACACAGTGTATA | 64326 |
rs375712110 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176014474 | ATCTGTTAGAAGTCA[A/T]TACCCTCAAAACAGG | 64326 |
rs375718053 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176125781 | TCATTGGTGTTTTGA[C/T]AGTGATTGCAATGTA | 64326 |
rs375726554 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176041473 | GTGCTTCAGCCACCC[C/T]CAGTAGCTAGGACCA | 64326 |
rs375792890 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176107072 | CTGCTGGGCTGTTCT[A/G]TATATCCATTGCCTG | 64326 |
rs375796956 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | RFWD2 | GRCh38.p7 | 1:176063542 | AAGCACAGATCAAAG[C/T]ATCAAGTTTTATAAC | 64326 |
rs375799638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176032654 | CACCATGTGGGCTTG[C/T]GACAACGCAGATGTT | 64326 |
rs375799755 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176004358 | TTCCTTCTCCTGCCT[A/G]ATTGCCCTGGCCAGA | 64326 |
rs375799921 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176085974 | TGTTTGAGCATTTAC[C/G]CTCAGAAGTTCATCA | 64326 |
rs375801484 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176062324 | ACCTGAATTTTTAAA[C/T]ACTGGCCAAAAGATT | 64326 |
rs375809742 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175982116 | GAAAATAATATGGAG[A/G]TCCTCAAATACTAAA | 64326 |
rs375819823 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175975109 | TTCACACCTATTCAG[A/C]GCCAACAGTTTCATT | 64326 |
rs375830636 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176083709 | TGGAAATAAAAGAGA[A/G]TACAGATGGATTTAC | 64326 |
rs375845604 | in-del | -/AGT | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176175197 | TATTCAACAAACCTG[-/AGT]TCCCGAGACCCATGG | 64326 |
rs375854904 | in-del | -/G | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:176103944 | TACTAAAGTTCCTAT[-/G]AAAAAACAAACAGGA | 64326 |
rs375855972 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175978192 | GGCATCAATTCTATG[C/T]TTCAAGATTGGCATA | 64326 |
rs375870001 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176040761 | CTCCATTATTTCATT[C/T]CTTTTATGTATTAAA | 64326 |
rs375926607 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176077925 | AAAGAAAATAACTAG[A/C/G]AACTCATCTAAGCAA | 64326 |
rs375928198 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176003244 | CATTCTAGATTCTGG[A/C]TATTAGCCCTTTGTC | 64326 |
rs375941539 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176169318 | TCATAAAATTATGTG[C/T]AATATTTATTTGTTT | 64326 |
rs375953034 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175997383 | CAATGGCAACAAAAG[A/C]CAAAATTGACAAATG | 64326 |
rs375963866 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175951205 | GGTGAGCCAAGATCA[C/T]GCCACTGCACTACAG | 64326 |
rs375964937 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176006266 | TGAGATGGGTTTCCT[G/T]AATACAGCACACTGA | 64326 |
rs375966923 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176029490 | ATAGATTTTCAGTAT[A/G]TAAGTTGTCATCCTG | 64326 |
rs375968180 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176147609 | AAAAAAAATTAATCA[C/T]AAACATTAGCTTAGA | 64326 |
rs375979431 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175961374 | TAGTGACTTTGGCAT[A/G]AAGTTTATTAATTTC | 64326 |
rs375980448 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176181873 | AAATAAACAAAAAAA[-/A]CACACGTTCTCATCA | 64326 |
rs376011617 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | RFWD2 | GRCh38.p7 | 1:175945674 | TTTAGAATTAAAGTA[A/G]TATACTGTCATAAAA | 64326 |
rs376028176 | in-del | -/CA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176073961 | CCTCTTTGTTTGAGA[-/CA]GAGTCTCATTCTGTT | 64326 |
rs376052506 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176168035 | AAGAGGATTATTCAT[C/T]AGAGAGGTAAGAAAA | 64326 |
rs376060245 | snp | A/G/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176122445 | AAAAAAATTTTGGAA[A/G/T]CTTATATATCATACA | 64326 |
rs376076416 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176199329 | TCTCAAAAAAAGATA[A/T]AAAAGAAATGCAAAA | 64326 |
rs376081623 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176050398 | TCAGTGTTTCCAATG[C/T]CTCTCATATCTTTTT | 64326 |
rs376087323 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176079336 | CTCTGCAGCAACATG[A/C]GTGAAGCTAGAGGCC | 64326 |
rs376121806 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176005084 | GTTTAGTCTTGGGAG[A/G]GTGTATGTGTCGAGG | 64326 |
rs376132115 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175986377 | TAAAACATAAGTGAA[A/G]AGTTTGAGGCAACTC | 64326 |
rs376135908 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175996241 | TAGGTTTTGATGGGA[C/T]ATATCTCAAAATAAT | 64326 |
rs376141394 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176040744 | TTACAGAATAGACTG[G/T]GCTCCATTATTTCAT | 64326 |
rs376148872 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:176062126 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 64326 |
rs376188549 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176171112 | CCTGGGCAACAGAGC[A/G]AGACTCCATCTCAAA | 64326 |
rs376197350 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176071129 | ATGGGAGGTGACTGA[A/G]TCATGGAGATGAATC | 64326 |
rs376197974 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175995495 | CAAAATTGATAGACC[A/G]CTAGCAAGACTAATA | 64326 |
rs376201919 | snp | A/G | 1.64923e-05 | 0.00287156 | intron-variant | RFWD2 | GRCh38.p7 | 1:176027548 | CCAACATCAAAGGAA[A/G]ACAAATCTGCTTTCA | 64326 |
rs376207140 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176096794 | GCTGTAGCCAATCTG[G/T]TCTGCTTTACATAAC | 64326 |
rs376209430 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176006799 | TTTTCCTTCATTTCA[A/G]CTTTGGTGAATCTGA | 64326 |
rs376226213 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176016058 | AAAGTAATGGGTTTG[A/C]AAAAGAAAAATTGAG | 64326 |
rs376226242 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176112681 | TAACTGTATTTTTGT[A/T]CCCATTAAGCAAGTT | 64326 |
rs376226444 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176060430 | TATATTTTTGTCCCC[A/G]AAGTTACTACGACAT | 64326 |
rs376231618 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176038204 | AAATACCTGCGAAAC[C/T]TGCATGCTGAAAATG | 64326 |
rs376252109 | in-del | -/ACAC | 0.00962287 | 0.0686938 | intron-variant | RFWD2 | GRCh38.p7 | 1:176132521 | TGTGTGTGTGTATAT[-/ACAC]ACACACATATATGAA | 64326 |
rs376271335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176195389 | TAGCACTGGAGATGA[C/T]TGAAGAATATGTAAC | 64326 |
rs376277191 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | RFWD2 | GRCh38.p7 | 1:175944729 | AGAGGTTGGGAAATA[C/T]GAACTTTACAAATTA | 64326 |
rs376279687 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176015361 | ATGCAGGTCCGAATC[A/G]TTGCAGTTTGCAGAG | 64326 |
rs376328647 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176017721 | GTAGAGATGAAGTTT[C/T]GCCATGTTGGCCAGG | 64326 |
rs376333220 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175996998 | ACCTGACTTCAAACT[A/G]TACTACAAGGCTACA | 64326 |
rs376341551 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176185008 | GTCACCAGAGCCCTT[-/TT]AAGAAAGCTCTACCA | 64326 |
rs376360254 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176178121 | GGAAATTTCACTGAA[A/G]GAAATAACATACTAA | 64326 |
rs376365608 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176166632 | AAATGGTTATTTTTT[C/T]CTTCTTGAAAAACGA | 64326 |
rs376416328 | in-del | -/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176016157 | GTCTGGAGTTTTTTT[-/T]AGCTAAGAGTGGAAT | 64326 |
rs376456554 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176028696 | GTGGTATATTTGTTT[C/T]ATATATATATATATA | 64326 |
rs376463669 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176004934 | AAGGAATGGTACCAG[C/T]TCCTCCTTGTACCTC | 64326 |
rs376469424 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175996602 | ATTCTTATACACCAA[C/T]AACAGACAAACAGAG | 64326 |
rs376474310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175989583 | AGTTTCACATATGAT[A/G]TCTAATCTCTAACAG | 64326 |
rs376480344 | snp | A/C/T | 6.68118e-05 | 0.00577945 | synonymous-codon | RFWD2 | GRCh38.p7 | 1:176046291 | TGTAACTCCAGCAAT[A/C/T]GCAAAATAGTCACAA | 64326 |
rs376481123 | snp | A/G | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176176818 | GTCTGAAAAAAAGAG[A/G]AAAAAAAGACAAAAG | 64326 |
rs376482875 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176194897 | CCTGAGCACCATGGC[A/G]AGACCCTGTCTCTAC | 64326 |
rs376482966 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175984925 | ATATTCTCTTCATAT[C/T]TAGGAATTAACTGAT | 64326 |
rs376515108 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176203719 | TGATAATACCTTCAA[C/T]CTTTTGTGTAAAATA | 64326 |
rs376543162 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176037338 | CATGAACCTGGGAGG[C/T]GGAGCTTGCAGTGAG | 64326 |
rs376562463 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175962299 | CCCAGTTACTTCCTG[C/T]ACCAGGAAAGGGATA | 64326 |
rs376574483 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176009629 | TGGAGTACTCATAAC[C/T]AGTTTGGTATGTTGA | 64326 |
rs376595550 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176156199 | ATATATTCAAGATTG[C/T]CTGCAAACATATTGT | 64326 |
rs376598009 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176181658 | CCATCCTGGCTAACA[C/T]GGTGAACCCCGTCTC | 64326 |
rs376598043 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176091738 | TGGGGGAGGTAAAAA[C/T]GTAAGAAAAAAAATC | 64326 |
rs376607127 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176036252 | CAATCTTCAAAAAAC[C/T]AGAAAGGGGAGGAAA | 64326 |
rs376648314 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176003460 | TATTGCCTAGGTTTT[A/C]TTCTAGGGTTTTTAT | 64326 |
rs376658294 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175993787 | TGTACCTGAAAGTGA[C/T]GGGGAGAATGGAACC | 64326 |
rs376659167 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175994011 | AAGGTCGGGTTAACC[A/T]CAAAGGGAAGCCCAT | 64326 |
rs376665637 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175980437 | AGTTTTGTTAGAAAT[C/T]AGAGAGAATAAAATT | 64326 |
rs376672282 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176125602 | CTGTTTTTATGCCAG[C/T]ACCATGCTGTTTTGG | 64326 |
rs376673294 | snp | A/G | 1.658e-05 | 0.00287919 | intron-variant | RFWD2 | GRCh38.p7 | 1:176043298 | AGACAGTAGCCTCAG[A/G]TAGAATACAGATCTC | 64326 |
rs376678922 | in-del | -/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176015828 | TGACAAGAACACTTT[-/T]AAGTGGAATTATGGT | 64326 |
rs376679286 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176106062 | TTGAGACAGAGTCTC[A/G]CTCTGCTGCCCAGGC | 64326 |
rs376697344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176082481 | TAACTGTTTGCATGA[C/T]GAAATTTATGTAACA | 64326 |
rs376698076 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176090062 | TCATCTACATAAAAA[C/T]TTTGTTCTTCACAAC | 64326 |
rs376712049 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176003868 | TGAACTTGAAAGTAG[G/T]TTTTTCCAATTCTGT | 64326 |
rs376736964 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175956689 | TGACATTTTGGTCAA[C/T]GATGGGTCACATATA | 64326 |
rs376760952 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176054041 | TGATCCTTAAGGAGG[C/T]ACTTAACACTAACTT | 64326 |
rs376773554 | in-del | -/GATGAC | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176110677 | AAAACAACAAAAAAA[-/GATGAC]AACAACCACAAAACC | 64326 |
rs376780055 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176007918 | CTAAGCAAGCCTGGG[C/T]AATGGCGGGCGCCCC | 64326 |
rs376780864 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175953613 | ATAAAAAAAGGAAAC[A/C]CTTTAAACATAAAAA | 64326 |
rs376786787 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175993715 | AATAAAAAGAAATGA[A/G]CAAAGCCTCCAAGAA | 64326 |
rs376789401 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175958612 | TATAACCCTTCTTTA[A/C]AATTTATTTCTCCAA | 64326 |
rs376799670 | in-del | -/GGT | 0.168785 | 0.236441 | intron-variant | RFWD2 | GRCh38.p7 | 1:176058183 | CCCGCCCGGTAGGGA[-/GGT]GGGGGGGGGTCAGCC | 64326 |
rs376801100 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175995559 | ATAAAAAATGATAAA[C/G]GGGATATCACCACCG | 64326 |
rs376863945 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176202447 | TCCTGCCCTGGCCTA[A/C]CAAAGGGCTGGGATT | 64326 |
rs376882644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176057844 | CTGCCCAGTCTGGGA[A/G]GTAAGGAGCGCCTCT | 64326 |
rs376892325 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176071150 | GAGATGAATCCCTCA[C/T]GGCTTGGTGCTATCT | 64326 |
rs376900420 | snp | A/C | 1.66743e-05 | 0.00288736 | intron-variant | RFWD2 | GRCh38.p7 | 1:176163002 | TTCTAAAAATGAAGA[A/C]AGAAGAAACACAACA | 64326 |
rs376907995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176196628 | AAATCATACAAAATA[C/T]ATGAAGACCCAAAAC | 64326 |
rs376911029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176177687 | TACCTCTTTTATTAC[A/G]TATCCAAATTACTAT | 64326 |
rs376912125 | in-del | -/AAAT | 0.00755907 | 0.0610114 | intron-variant | RFWD2 | GRCh38.p7 | 1:176189645 | AACTAGGATGTACAC[-/AAAT]AAAGAGCTCTAAAAA | 64326 |
rs376924023 | in-del | -/CTTT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175965592 | GTTTTGTTTTTGTTT[-/CTTT]GTTTGTTTGTTTTTG | 64326 |
rs376924451 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176004168 | GTCTGTTGTTGGTGT[A/G]TAAGAATGCTTGTGA | 64326 |
rs376934504 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176154581 | AAGTGAGAACTAAAC[A/G]ATGAGGACACATGGA | 64326 |
rs376962529 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175947845 | AAAAGAAACAAAGAC[A/T]GAAATAAAATGAAAA | 64326 |
rs376979478 | in-del | -/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175947743 | AGTGTAAGTTTTAAT[-/T]AAAAGAATAAAGTTA | 64326 |
rs376983016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175972895 | TGGAGTGCAATGGCA[C/T]GATCTTGGCTCACCA | 64326 |
rs376988476 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176184022 | TTGTACAATAATATG[A/G]ACATACTTAACACTA | 64326 |
rs377000526 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176139982 | AAAAGAAAGTAAATA[C/T]CTGTAATATCAATAG | 64326 |
rs377017099 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176151742 | TGCTTTAGTATCCTT[C/T]GGTTATATGGCAAGT | 64326 |
rs377026050 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175962813 | TATCTCTTAACAAAA[C/G]TCTTCAATTCACATG | 64326 |
rs377029220 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176165889 | AAGGAGAGAGCATGA[A/C]ATAATTCAGTGGGAA | 64326 |
rs377084890 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | RFWD2 | GRCh38.p7 | 1:176005717 | CTGTGGTATGAGAGA[C/T]AGTTTGTTATAATCT | 64326 |
rs377085063 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176192680 | TACCAAGTTCACACA[C/G]AAGAAAAACAAATGC | 64326 |
rs377085472 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175952314 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGTGG | 64326 |
rs377136905 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176092270 | TCTGAAGCATGCATA[A/G]AACATTTACAAAAAC | 64326 |
rs377140685 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176083703 | AATAGTTGGAAATAA[A/T]AGAGAATACAGATGG | 64326 |
rs377151325 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175995927 | CCTGATACCAAAGCC[A/T]GGCAGAGACACAACC | 64326 |
rs377188051 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176188866 | ACACACACAGACAGA[C/G]AACAAAGCATCCCAG | 64326 |
rs377195108 | snp | G/T | 1.65608e-05 | 0.00287752 | intron-variant | RFWD2 | GRCh38.p7 | 1:176043675 | ACAAACCAAATGTAT[G/T]ATTCATATAACATGT | 64326 |
rs377203998 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175965990 | AACCAAGTGAGAGTC[C/T]ATACAAAGACATTCA | 64326 |
rs377220760 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176170605 | CGCTGAAAAGAGATA[C/T]GCTGTCTTCAGGCTT | 64326 |
rs377224201 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176025822 | TTGAGCCAGGGAGGA[A/C]CAGGCTGCAGTGAGC | 64326 |
rs377235936 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176013324 | CAGAAATTTACTTAG[C/T]TAGGGGGAAAAACAC | 64326 |
rs377293588 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176019128 | CTGAGATTGCACCAC[C/T]GCACTCCAGCTTGGG | 64326 |
rs377354843 | in-del | -/ATTT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175976195 | GGGAAAGGTATAACT[-/ATTT]TATTCTGTTCAGAAT | 64326 |
rs377355208 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176186662 | AGGAGTGATGGGATT[A/C/T]GACACAGTAATGAAC | 64326 |
rs377369789 | snp | C/T | 0.000152586 | 0.00873324 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176206721 | GCAGCTGTGCCGGGA[C/T]AGGCCCGTGGACACC | 64326 |
rs377382022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175954214 | GGATGGAAATGAGAA[A/G]CCATTTTGAACTAAA | 64326 |
rs377413111 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176004781 | GAGGATTTTTGCATC[A/G]ATGTTCATCAAGGAT | 64326 |
rs377441144 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176023878 | CCAATTCTTCACAAA[C/G]TCATTCAGAACGCAG | 64326 |
rs377455445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176196733 | GAAGGGGAACATTCC[A/G]TATCGTCTTTTAGAA | 64326 |
rs377455784 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176011628 | ACTCAAAATGTGAGC[C/T]TCAAAATAGTAACTG | 64326 |
rs377457784 | snp | C/G | 0.000115431 | 0.00759618 | intron-variant | RFWD2 | GRCh38.p7 | 1:176027555 | CAAAGGAAGACAAAT[C/G]TGCTTTCATTTCTTA | 64326 |
rs377480820 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176127915 | CACTTGTTTCATCTT[C/T]CTGATAATGGCCAAT | 64326 |
rs377492658 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176118711 | CAATGAGCTATGCAT[C/T]GCTGCATTCCAGCCT | 64326 |
rs377505437 | snp | C/T | 0.00011832 | 0.00769065 | intron-variant | RFWD2 | GRCh38.p7 | 1:176085771 | GAGAAGGTCTAAATA[C/T]ATACCTGAGATACGA | 64326 |
rs377510370 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176042046 | GAACCTGGGAGGCAG[A/C]GGTTGCAGTGAGCGG | 64326 |
rs377519521 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | RFWD2 | GRCh38.p7 | 1:175994057 | TCTCTGGGCAGAAAC[C/T]CTACAAGCCAGAAGA | 64326 |
rs377521096 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176162178 | TCTAATCTTCTCAAA[-/A]GTTTGGTGGTTCAAC | 64326 |
rs377538785 | in-del | -/AGAAAGAAAGAAGGAA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176151326 | GAAAGAAAGAAGGAA[-/AGAAAGAAAGAAGGAA]GGAAAGAAAGAAAAA | 64326 |
rs377545494 | in-del | -/GT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175980019 | TATCGCTTTTGCTGT[-/GT]ATCAGGAACTGTTCC | 64326 |
rs377551464 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176193303 | TGGAGAAATTAGAAC[C/G]CTTATACATTGCTAG | 64326 |
rs377574988 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176172952 | TGTTATTTCCACAGT[G/T]GACAACAATATAATC | 64326 |
rs377577775 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176000775 | ATGCCTCCATTATTA[C/T]CTTACTTTGTGTTAT | 64326 |
rs377579343 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176007291 | GCCTTTGGTTTGCAT[G/T]TCCTCCCGTAGCTCA | 64326 |
rs377584180 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176131508 | CATATAATAAAGATA[C/T]TCATTATAGAAAACT | 64326 |
rs377594893 | in-del | -/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175946737 | CTGAGGAAAAACCTA[-/C]TTCTTAGGGGACAGA | 64326 |
rs377610546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176008527 | TATTTTCCTTTAACT[C/T]TTTGTGGTTTAATTA | 64326 |
rs377610826 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176055035 | CAACAATAGCTGACA[C/T]TGATGATCACTCTCT | 64326 |
rs377610937 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RFWD2 | GRCh38.p7 | 1:175990777 | TCTGTTCGACCTAAA[C/T]ATAGCCATTCTACCA | 64326 |
rs377612029 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175997314 | AAGAAAACCTAGGCA[A/T]TACCATTCAGGACAT | 64326 |
rs377612465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175972661 | AGTAGAGACGGGGTT[C/T]CACCATGTTGGCCAG | 64326 |
rs377624352 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176074209 | TGGGATTACAGGTGT[G/T]AGCCACCTCACCTGG | 64326 |
rs377643118 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176160872 | CTTTCTTACCACCTC[C/T]GTTGGGGGTGGAGGG | 64326 |
rs377644005 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176170953 | ACACAGTGAAACCCC[A/G]TCTCTACTAAAAATA | 64326 |
rs377653185 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176093233 | TTGGTTAGGAACACA[A/T]GAGTAACCTGTATAC | 64326 |
rs377654833 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176070460 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 64326 |
rs377680340 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176007376 | ATCCAGCTTTGTTCC[A/G]TTGCTGGTGAGGAAC | 64326 |
rs377681067 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176077903 | CAATCTTATTTACAA[C/T]AGCCACAAAGAAAAT | 64326 |
rs377682944 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:176001764 | GCAGAACTCTCTCTG[C/G]TATTTCTTATGGGGT | 64326 |
rs377683493 | in-del | -/TACGTATATACG | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176133177 | ACGTATGTACACACA[-/TACGTATATACG]TACGTATATGTACGT | 64326 |
rs377700975 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176120434 | CTATCTCCAAAAAAT[-/A]AAAAAAAAAAAGCTT | 64326 |
rs377726867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176164943 | AAGAAGTATTAGCAC[A/G]GAGAGCATAAGTAAC | 64326 |
rs377729729 | snp | C/T | 6.59402e-05 | 0.00574158 | intron-variant | RFWD2 | GRCh38.p7 | 1:175947192 | ATATAGTAAATAGCT[C/T]ACCTTAATTGTACCC | 64326 |
rs377745220 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176190031 | AGATGGAAAAAAAAA[-/A]GATGGTTATTATAGG | 64326 |
rs377749203 | snp | A/C/T | | | utr-variant-5-prime, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207202 | AGTAGAAGGCACTAC[A/C/T]GCTGTCGAGGCCGCC | 64326 |
rs386354370 | in-del | -/AA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176181428 | TTTAAACAAAACTGC[-/AA]AAAAAAAAAAAATCA | 64326 |
rs386368797 | in-del | -/GTTT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175965601 | TTGTTTGTTTGTTTG[-/GTTT]TTTTTGAGATGGAGT | 64326 |
rs386636996 | in-del | GTT/TG | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175965583 | TTTTTTTTTTGTTTT[GTT/TG]TTTGTTTGTTTGTTT | 64326 |
rs386636997 | multinucleotide-polymorphism | CTC/TTT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175976809 | AAAATATTTAGATAG[CTC/TTT]GTAATGAAATAAGAC | 64326 |
rs386636998 | multinucleotide-polymorphism | CG/TA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176018144 | TGCACTAATGTTAGC[CG/TA]TTATTATTTACCCTT | 64326 |
rs386636999 | multinucleotide-polymorphism | AG/GA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176148495 | TAGTGTGAAATGACT[AG/GA]GAAATTTTATAAATG | 64326 |
rs386637000 | multinucleotide-polymorphism | CGACAGGG/TGACAGGA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176168244 | TTGTATCTTTAGTAG[CGACAGGG/TGACAGGA]TTTCACCATGTTGGC | 64326 |
rs386637001 | multinucleotide-polymorphism | GC/TT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176173757 | CTTTGGGAGGCTGAG[GC/TT]GGGAGGATCGCTTGA | 64326 |
rs386637002 | multinucleotide-polymorphism | AGG/GGA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176203951 | CCCAGCCTCCAATTC[AGG/GGA]TACGTCTTCTTGGGA | 64326 |
rs397688433 | in-del | -/TGT | 0 | 0 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176208575 | TTGGGAATAAAGTGT[-/TGT]GAAAATACTCATGAC | 64326 |
rs397706639 | in-del | -/A | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176194937 | TAAAAAAAAAAAAAA[-/A]TCAACCAGATGTGGT | 64326 |
rs397708682 | in-del | -/G/GT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176009889 | CTTGGGGGGGGGGGG[-/G/GT]TCCGCAATAATTTTC | 64326 |
rs397718692 | in-del | -/ACAC | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176187427 | GAGATCCTGTCTTAT[-/ACAC]ACACACACACACACA | 64326 |
rs397733609 | in-del | -/GTTT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176121515 | CTTTAAATGTCGTTT[-/GTTT]TTTATTTTTATGTTT | 64326 |
rs397748055 | in-del | -/T/TC | 0.00953873 | 0.0683987 | intron-variant | RFWD2 | GRCh38.p7 | 1:176084860 | CAGACTTTTTTTTTT[-/T/TC]CCCCCTTGGTGGGGT | 64326 |
rs397799297 | in-del | -/T | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:175964432 | AATCATCTTCTGGGC[-/T]TTTTTTTCCCCAGTA | 64326 |
rs397802760 | in-del | -/GT | 0.375 | 0.216506 | intron-variant | RFWD2 | GRCh38.p7 | 1:176199398 | TGAGTTCTCTGCCAA[-/GT]GTATGTTTAGTTTTA | 64326 |
rs397811775 | in-del | -/T | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176058854 | CACGCCTCCTCAGAT[-/T]CCCATATGTGAGTTA | 64326 |
rs397828319 | in-del | -/A | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176122157 | AAAAAAAAAAAAAAA[-/A]TCTGGGCTCAAAAAG | 64326 |
rs397830336 | in-del | -/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176056441 | ACACAGGGATTTTTT[-/T]AATATATAAAGATAC | 64326 |
rs397831058 | in-del | -/G | 0.5 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176022745 | TGCTTCAGACCGAGG[-/G]AAAATTAGCTCATAC | 64326 |
rs397954354 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176178351 | ACAAAAAAAAAAAAA[-/A]TAATAATAATAAATG | 64326 |
rs397957058 | in-del | -/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176167969 | AGCCATTTTTTTTTT[-/T]AAACAGGGATTTTAC | 64326 |
rs397965708 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176094687 | TAAAAAAAAAAAAAA[-/A]GTCCTCAAATAAATG | 64326 |
rs397982014 | in-del | -/T | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:175952439 | TTCTTGTTTATCATC[-/T]TTTTTTTTTTTTTTT | 64326 |
rs397982015 | in-del | -/C | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:175958377 | GGCTTTGATATTATA[-/C]CTGAATGGTTACAGA | 64326 |
rs397982016 | in-del | -/A | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:175965050 | TATAATCTTGGTATG[-/A]AAAAGAGCTTAAGGC | 64326 |
rs397982018 | in-del | -/T | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:175979511 | TTTCACAACTCAGTC[-/T]TTTTTTTTTTTTAAA | 64326 |
rs397982019 | in-del | -/T | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176027913 | AGTCAATTAAACCTC[-/T]TTTTTTTTTTTTTAA | 64326 |
rs397982020 | in-del | -/T | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176039592 | TGAATTTTAAGGTAA[-/T]TTTTTTTTTTTCTGT | 64326 |
rs397982021 | in-del | -/T | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176042288 | CAGACATGAGCCACC[-/T]TTTTTTTTTTTTTTT | 64326 |
rs397982023 | in-del | -/A | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176054177 | GTGAGGCACCATCTC[-/A]AAAAAAAAAAAAAAA | 64326 |
rs397982024 | in-del | -/A | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176086243 | GTGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 64326 |
rs397982025 | in-del | -/T | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176094045 | CGTTAAACAGATCAC[-/T]tttttttttttcctt | 64326 |
rs397982026 | in-del | -/A | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176099141 | CAATTGTCTGTGAAT[-/A]ACAAAATGTCCAGGG | 64326 |
rs397982028 | in-del | -/A | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176108046 | TAATGTCCTTTATAG[-/A]AAAAAAAAAAAATCT | 64326 |
rs397982029 | in-del | -/AA | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176113960 | CACTGTGCAAACTAT[-/AA]AAAAAAAAAAAAAAA | 64326 |
rs397982031 | in-del | -/ACAC | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176127583 | TATATACACATACAC[-/ACAC]ACACACACACACACA | 64326 |
rs397982032 | in-del | -/AC | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176127611 | TGTATATATATATAC[-/AC]ACACACACATATATA | 64326 |
rs397982033 | in-del | -/TTT | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176173344 | CTGGCCAATTACTGG[-/TTT]TTTTTTTTTTTTTTT | 64326 |
rs397982034 | in-del | -/T | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176174570 | TACTCTTCACTGTAA[-/T]TTTTTTTTTATGAAG | 64326 |
rs397982035 | in-del | -/T | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176190543 | ATCTGTTCTGTACTG[-/T]TTTTTTTTTTTTTAA | 64326 |
rs397982036 | in-del | -/A | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176202206 | TGAGACCCTGTCTCC[-/A]AAAAAAAAAAAAAAA | 64326 |
rs398053554 | in-del | -/AA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176000350 | CTGGCATTTATTGAA[-/AA]GACTGTCTTTTCTCC | 64326 |
rs398053556 | in-del | -/ATGCCT | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176145396 | GCTCATACAATGCCT[-/ATGCCT]GTAGGAAGAATAACT | 64326 |
rs398074433 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175979510 | CTTTAAAAAAAAAAA[-/A]AGACTGAGTTGTGAA | 64326 |
rs398074434 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176088263 | TATCATAAAAAAAAA[-/A]AGAATGAGCTGCTGA | 64326 |
rs398074435 | in-del | -/A | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176176824 | AAAAAAGAGAAAAAA[-/A]AGACAAAAGAAAATA | 64326 |
rs398089684 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176135940 | CAAAAAAAAATTACA[-/A]TACATATAAATAACT | 64326 |
rs398103389 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175953298 | AATACTCAAAAAAAA[-/A]GAAAGGAAATGAGGA | 64326 |
rs398103390 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176078629 | TTGCAAAAAAAAAAA[-/A]CAAAAATTGACAAGT | 64326 |
rs527238472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176057596 | CCAGCCTCGGCCTCC[C/T]GAGGTGCCGGGATTG | 64326 |
rs527273076 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176078991 | GTCAAAAAATAACAG[A/G]TACTGGCAAGGCTGT | 64326 |
rs527280097 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176148131 | ATAACAGATGTTTGT[C/T]AGTAGGAATATTAAA | 64326 |
rs527282638 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176140900 | TCAATAGCAAGCACT[C/G]TCTTAACACTGTGCC | 64326 |
rs527291133 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176140600 | AAGGATGTGGAAAGA[A/C]GAAATGGGCTAAATT | 64326 |
rs527291601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175969741 | GTGAGAAAAATCTTT[C/T]CTCCCTTACAGCATG | 64326 |
rs527291684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175962740 | GTGTTCTATTCCTTC[A/G]GCCATCTCTCACCGC | 64326 |
rs527319275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176141387 | GCACCTGTAATACCA[A/G]CTACTTGGGAGGGTG | 64326 |
rs527319566 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176004113 | ATTCTCTTTGAAGCA[A/G]TTGTGAATGGGAGTT | 64326 |
rs527322491 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176105768 | TCAGTTGGTCAGCAT[C/T]GTTTAGTAATAATAA | 64326 |
rs527339243 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176055062 | CTCTCTTCCACAATA[C/G]AGTGATTTTTCTCCT | 64326 |
rs527343606 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176202999 | TGAATGGTAGATCTA[C/T]TTAATGTAGATCCTA | 64326 |
rs527344203 | in-del | -/T | 0.215144 | 0.247558 | intron-variant | RFWD2 | GRCh38.p7 | 1:175990906 | AAAGCTGGATTCTAA[-/T]TTTTTTTTTTTTTGT | 64326 |
rs527349973 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176014749 | ATGTGTGTGTATGTA[A/T]ACATACATATATATG | 64326 |
rs527364563 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176183267 | CGATATCATATCCAA[C/G]TTCAGCATAAAATTA | 64326 |
rs527385489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176147652 | TCAAGCGAAAAAGTT[C/T]TACGGCATGATTCAT | 64326 |
rs527397065 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176057128 | AATATTTGCTGAACA[C/T]TCCAAACTTACTAAT | 64326 |
rs527401521 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176080991 | GAGACGAAGAAATTT[C/G]GCATATAGAAGCTCA | 64326 |
rs527401534 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176053055 | GACACATAAGCAAGA[A/G]TACTCTTAAATACAC | 64326 |
rs527401536 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176008049 | TATAATCTCGTGGTG[A/C]GCCGTTTTTTAAGCC | 64326 |
rs527406736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176099721 | GGAGTCAAGCTCGAC[C/T]TGCAGAGCCAATAAA | 64326 |
rs527426541 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175975558 | GGGATTATAAGCATG[C/T]GCCAATATGCCAGGC | 64326 |
rs527435669 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176126178 | AACAGGGATAATTTG[A/T]CTTCTTCCTTTCCAA | 64326 |
rs527438011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176134109 | CCTTTCTGTACATGA[C/T]GTACTGAACTAGATC | 64326 |
rs527445248 | snp | C/T | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176185437 | AATCCTCTTCTGCCC[C/T]CTTTCCCTATAAAGA | 64326 |
rs527465340 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:175993980 | AAGGAAAAAATGTTA[A/G]GGGCAGCCAGAGAGA | 64326 |
rs527474687 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176026082 | CATGGAAAATTAAAT[A/G]AGAAAAATAACTAAG | 64326 |
rs527479578 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175956083 | AGGGACTTACACAAC[A/T]TGATTTGAAGTTCTA | 64326 |
rs527493023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176169269 | CACACCTTGGTAAAC[A/G]GTACATTCACTATAG | 64326 |
rs527519472 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176120205 | GCAGGCGGATCACCT[C/G]AGGTCAGGAGTTCAA | 64326 |
rs527552486 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175963355 | TTAGACACTTTATTA[C/G]AAGTTTCTTAAACAT | 64326 |
rs527574343 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176004617 | GAGATAATCATGTGG[A/T]TTTTGTCTTTGGCTC | 64326 |
rs527574402 | in-del | -/TTTTTTCT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176041353 | TTTTTTCTTTTTTTC[-/TTTTTTCT]TTTTTTTTTTTTGAG | 64326 |
rs527576821 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175998808 | GTAATCCTAGGTAGG[A/C]TAAGGTAAAGCCTAG | 64326 |
rs527598650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176133280 | TACGTATATATATAC[A/G]TATGTACACATATAT | 64326 |
rs527609751 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176169987 | AGCATCTTCACTAGG[A/T]GTAGATTTCATCTCA | 64326 |
rs527613552 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175998621 | TCTGCAAATTATGAA[A/C]TCTTTCATCTAGTAC | 64326 |
rs527618274 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176028372 | AGTTAAGAGACTAGC[C/G]TGGGCAACATGGTGA | 64326 |
rs527625299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176086375 | GGACTACAGCCGCCC[A/G]CCACCACGCCCAGCT | 64326 |
rs527650353 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992840 | ACAAAAAGACAGCAG[A/T]AACCTCTGCAGACTT | 64326 |
rs527654709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176084289 | TTGGGAATCTTAATA[C/T]CCAGAAATTGTTAGA | 64326 |
rs527657526 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175997666 | CTCATCATCACTGGC[C/T]ATCAGAGAAATGTAA | 64326 |
rs527660767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175961364 | CATTATACAGTAGTG[A/G]CTTTGGCATGAAGTT | 64326 |
rs527674166 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176035410 | TCTATGAGACAGAAC[A/G]AAAGGGTCTAATACA | 64326 |
rs527696350 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176173757 | CTTTGGGAGGCTGAG[G/T]CGGGAGGATCGCTTG | 64326 |
rs527725084 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176124991 | GATATTTCATTGTAG[G/T]TGTGATTTGCATTTC | 64326 |
rs527728187 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:175954017 | TTTTCAAATGCATGC[A/G]TACTAGTCCCCAACA | 64326 |
rs527732678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176090349 | CTCTTGAGACTATGC[C/T]TCAGGCCAGGGTCAC | 64326 |
rs527759410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176041593 | GCCTCAAGTGATCCA[C/T]CCGCCTCAATCTCCC | 64326 |
rs527760195 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176049471 | AACAAGATCCTTTTA[A/T]ACTGTAAAAATAGAT | 64326 |
rs527782220 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175980003 | ACTAATAGCAAACAT[A/G]TATCGCTTTTGCTGT | 64326 |
rs527786396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176003226 | TGTAAATTTGTTTGA[A/G]TTCATTCTAGATTCT | 64326 |
rs527793996 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176139907 | TTAGCATCACACCAT[A/G]TATCTACGTAAGAAA | 64326 |
rs527794711 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176110760 | TGAAGCCATAATGTC[C/T]GGGTTAAAATCTCAG | 64326 |
rs527803369 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176131299 | AGATGAGGTGATGCT[A/T]AGGATCTAAACAAGG | 64326 |
rs527818146 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176083537 | ACACATATCTGCTGG[A/T]ATATCACCTCTCCTA | 64326 |
rs527830206 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176179893 | GGACATAGCTGGAAG[G/T]AACTGTCCTCACTAA | 64326 |
rs527843461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176111887 | TGCAATGTATCATGT[C/T]AGCTCCATCTCAACA | 64326 |
rs527843794 | snp | A/C | 0.000172013 | 0.00927238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175982398 | CTTCCTCTTCTACCA[A/C]TCCAGAGAAAGACCA | 64326 |
rs527849073 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176142998 | GCAGGATGGAAATAA[C/T]AAAGAACATAAATAA | 64326 |
rs527869151 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176071794 | AACACTGGTTTGTGA[A/C/T]AAACCTTCACAAGTC | 64326 |
rs527884061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176161771 | TATGGTTAAAACCGT[A/G]AGAGAAATTCCCATT | 64326 |
rs527889650 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | RFWD2 | GRCh38.p7 | 1:176119285 | AACACTAATAAAATT[A/G]TGTAGTTGCATATTT | 64326 |
rs527890774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176112386 | GTTACGTATATATAC[A/G]TGTGCCATGTTGGTG | 64326 |
rs527903483 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175983067 | AGCATGTGAGATGAC[C/T]GATATGCTCATTAGT | 64326 |
rs527910137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175975026 | CTCATTTTTAAAAAA[C/T]ATTGACAGCTGTCAG | 64326 |
rs527918223 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176200719 | CATGTTACTCTCAGT[A/G]AATATATTGTTTGAG | 64326 |
rs527920139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176014177 | AAACAGAAAGTAAGA[A/G]AATACATCTGACTAC | 64326 |
rs527943958 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176064109 | GACGGATCTTTCAAA[A/G]CTAGGTAATGGGTCA | 64326 |
rs527947560 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175945915 | TTTATATTAGGTAAC[A/T]AGGCTACTTAACATA | 64326 |
rs527947593 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176131331 | AGAAGCAGTAAAATA[C/G]GATATGACAATTACA | 64326 |
rs527950237 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176028818 | GAGTGCAGTGGCACA[A/C]TCATGCCTCACTTCA | 64326 |
rs527962476 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175993216 | AACTAACAAACAGAA[A/G]GGACATCCACACCAA | 64326 |
rs527964000 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176125533 | CAAAAACGAGTTCAC[C/T]GTAGGTGTGTGGATT | 64326 |
rs527994240 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176071077 | TGCCCAAATCTCATA[C/T]TGAACTTGTAATCCA | 64326 |
rs528009008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176168299 | CCTGACCTCGTGATC[C/T]GCCCGTGTCAGACTC | 64326 |
rs528026416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176161125 | TTCAGTTTCCTCAGA[C/T]CTACTTATCTGTTAC | 64326 |
rs528027604 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176194590 | TTGCAGTGAGCCAAG[A/G]TAACACCACTGCACT | 64326 |
rs528059808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175949583 | CCTGTAAACATCATC[C/T]AGAAAAGCAGTTGAA | 64326 |
rs528072492 | snp | A/C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176088731 | CCGGGCGCAGTGGCT[A/C/T]GTACCTGTAATCCCA | 64326 |
rs528076335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176031837 | AAAAATCCAACTACA[C/T]TACAGAATAAAGTAT | 64326 |
rs528112920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176122410 | AGGAATATGACTATA[C/T]TCTGACCCAAAAGAT | 64326 |
rs528135752 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176055317 | GCAGGCACCTGTAAT[C/T]CCAGCTACTCAGGAG | 64326 |
rs528138584 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176095944 | TGCATTAAATCCAGG[C/G]CTTTGCATGTATACC | 64326 |
rs528140840 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176176549 | GCCAGTAAGGCACAA[C/T]GGCTCATGCCTGTAA | 64326 |
rs528148489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175957990 | AACTTATGATAACAT[A/G]AAGTGGATTAGCAGT | 64326 |
rs528156708 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176000635 | ACAATGTAAATATTT[A/T]TAAAAAAATGAAATC | 64326 |
rs528157894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176183072 | ATTTTAATACTTTAT[C/T]TTATAAGAAAGAATA | 64326 |
rs528191191 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176170372 | TGAAATGTGTTTCTT[C/T]AATAATAAGACCTGA | 64326 |
rs528204254 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176007136 | TCCAGTTGATCGCAT[A/C]GGCTCCTGAGGCTTC | 64326 |
rs528216773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175994736 | ACAGGAGCACCCAGA[C/T]TCATAAAGCAAGTCC | 64326 |
rs528219183 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176080493 | TGGCTCTCTGGGAAG[A/T]TCAATAAAACTGATA | 64326 |
rs528231136 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:175986174 | ACAGTCACCCGCCAC[C/T]ACGCCTGGCTAATTT | 64326 |
rs528252770 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176115668 | GCAGGAGAATCACTT[C/G]AACCCAGGAGGAGGT | 64326 |
rs528263584 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176115477 | AAAATGGCTGAGCAC[A/G]CTGGCTCACGCCTGT | 64326 |
rs528266633 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176060276 | AACTTTTGTGAATAT[C/T]AAGTGTTTATTTTGT | 64326 |
rs528270959 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176147199 | CAATTATATTCATTT[C/T]GAAGATTAAACACGC | 64326 |
rs528273274 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176109427 | CACCTTTATCACAGA[C/G]TATTAATTACTTTTT | 64326 |
rs528280041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176067977 | AGCCACACCCCCATC[A/G]CACACCCTGCAAGGG | 64326 |
rs528294318 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175987606 | TATTCTATTAATGGT[C/T]TATGAACTGTATTTT | 64326 |
rs528320813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176019101 | AACCTGGGAGGCAGA[C/T]GCTGCAGTGAGCTGA | 64326 |
rs528356306 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176025330 | GCAATTACTGCTTTG[C/G]GCAGATATCAAGTAT | 64326 |
rs528361111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176203950 | CCCCAGCCTCCAATT[C/T]AGGTACGTCTTCTTG | 64326 |
rs528363823 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176122995 | ATTTGACTCCAACAA[A/C]ATAAGTTAAAGTTTC | 64326 |
rs528373641 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176075159 | ATTTTTTGTTAATTA[A/C]ATTATGTAATAAAAT | 64326 |
rs528387308 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176118122 | ATAACCTGACTCTGG[A/G]CAAGTGATTAATCTT | 64326 |
rs528395469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176018358 | CTCAGTTATATTATG[C/T]ACATTTTCCCACAAT | 64326 |
rs528439161 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176113590 | GTGGAAACCTTTTCT[G/T]GTTCCCCTATATAAA | 64326 |
rs528445763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176156152 | GAACCAAAAAAAGGG[A/G]AAGTTTAGTAAACTG | 64326 |
rs528452469 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176209127 | TTTTGTGATAGTTTT[G/T]GTCATCAGGTGTGCA | 64326 |
rs528453881 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176059532 | CTGTTGCCCAGGCTG[G/T]ACTGTGATGGTGTGA | 64326 |
rs528469431 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176066146 | TGTTGACCCTAGAAG[C/G]TCAAAGTCCCTTTCC | 64326 |
rs528481794 | snp | C/G | 0.0252325 | 0.109451 | intron-variant | RFWD2 | GRCh38.p7 | 1:176028852 | AGCCTCTACCTCCTA[C/G]GCTCAGGTGATTCTC | 64326 |
rs528494617 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176058358 | AAAGATTGAGAAATC[A/G]GATGGTTGCTGTGTC | 64326 |
rs528495556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176107971 | ACTGTACCAATTTAG[A/G]GGAGATTAAAGAGAC | 64326 |
rs528509500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176016811 | CAAAAAAATTTATCT[A/G]CTTAAATCAGCATTC | 64326 |
rs528516676 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176066671 | AAGACCAGCTCTGCA[C/G]GTCAATCACCAAGAT | 64326 |
rs528558645 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176079495 | TGGGGAGGTGGGAGA[A/C/G]GGCAGGGGTCGTGGG | 64326 |
rs528569951 | snp | C/G | 0.0517044 | 0.152246 | intron-variant | RFWD2 | GRCh38.p7 | 1:175994269 | TGGAAAGGAACAACC[C/G]ATACCAGCCACTGCA | 64326 |
rs528616111 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176052878 | TTTGACCATCATTTC[A/G]TATCAGCACATATGA | 64326 |
rs528617235 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175947585 | ATGTTGGTCAGGCTG[C/G]TCTCGAACTCCCAAC | 64326 |
rs528629450 | in-del | -/A | 0.00151363 | 0.0274686 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176176024 | TATTAGTAGGGGGGG[-/A]AAAAAAAGGCTTAAT | 64326 |
rs528644063 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175990533 | AAGTCTTCTAAAACT[A/C]TGCCAATTTTCTGTC | 64326 |
rs528664765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176182512 | GGGGTCAAGTATACT[A/G]CTAAACAATCTATAA | 64326 |
rs528667281 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RFWD2 | GRCh38.p7 | 1:176005516 | TTCCCTCTACACACT[A/G]CTTTGAATGTGTCCC | 64326 |
rs528685129 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, missense | RFWD2 | GRCh38.p7 | 1:175971960 | CACTCCTGTAAAGAA[A/C]GAATAGGTTTGCGGC | 64326 |
rs528697596 | in-del | -/AAAA | 0.00993419 | 0.0697739 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176186355 | TACAAAAAAAAAATT[-/AAAA]AAAAAAACACAAAAA | 64326 |
rs528704874 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176080667 | TCAACAGCCCTGATG[A/C]GACGGACAAATGTCT | 64326 |
rs528713836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176143761 | AGACACCCCTGGGCC[A/G]ATCAGGATGGTTGGT | 64326 |
rs528714294 | in-del | -/AC | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176107894 | ACAAGACAAATTCAA[-/AC]TGAGGGAAATCCTAT | 64326 |
rs528725446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176156722 | CATTTCATAATAATA[A/G]TAAAGGAGATGATTC | 64326 |
rs528752441 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175992834 | GCACAGACAAAAAGA[C/T]AGCAGTAACCTCTGC | 64326 |
rs528756346 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176150215 | CTATGCCTCTTGCAG[A/T]TCTTTGGATTTTAAA | 64326 |
rs528779085 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176017500 | TGGTTACTAATATTT[A/T]TCTCATACAGATATC | 64326 |
rs528781944 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176108532 | CTTCCTGGACGACTA[A/T]CAACTCAACTACCAC | 64326 |
rs528782482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176149701 | AACAGATAAATGAAA[A/G]TATAATAAGCCTTGA | 64326 |
rs528791910 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176008960 | ATGTTGTGGAATGCT[G/T]TCAGAGCTTAAATCT | 64326 |
rs528798738 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176013633 | ATGTATTTCAACTCA[C/T]CATATAATATGTGAA | 64326 |
rs528801997 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176005143 | GTTTATTTGTGTAGA[C/G]GTGTTTGTAGTATTC | 64326 |
rs528813730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175978506 | ACTAGGGTTGCCTCA[A/G]TTTTCTACCACCTTC | 64326 |
rs528813839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176015980 | ATGCTTCAATTTAAC[A/G]TGAAGAATGAGATAC | 64326 |
rs528815012 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175991349 | ATTTACGTATCTAAA[C/T]ATAGAAAAGCTACAG | 64326 |
rs528817324 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176192726 | TATAAAAACAGGAAT[C/T]TCTATTACAGTATAA | 64326 |
rs528831903 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176120667 | TGTCCGTATAACTAT[A/T]TTCACCTAGATTATT | 64326 |
rs528847046 | snp | G/T | 0.0693013 | 0.172766 | intron-variant | RFWD2 | GRCh38.p7 | 1:176199174 | TACAAAAAATTAGCT[G/T]GGCATGGTGGCGGGC | 64326 |
rs528847290 | snp | C/T | 0.000528262 | 0.0162435 | missense, utr-variant-5-prime, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176206935 | GCCGAGGACCCGGGG[C/T]TTGTCCCAGCGGAGC | 64326 |
rs528848431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176111138 | GCCTGGACAACAGAG[C/T]GAGACCTTGTCTCAA | 64326 |
rs528858199 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176152901 | AATAATTTTTCTCTA[A/G]AACACTACAGTATTT | 64326 |
rs528871706 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176029824 | TTACGTAAGAATTTA[A/G]TATGTGAAATCTCCA | 64326 |
rs528882167 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176195160 | GGGAGAAGAGAGGGA[A/G]AGAGGAAGGGAGGGA | 64326 |
rs528884555 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175974294 | GATACATACATACTG[C/G]TTTTGCATTTGTAAG | 64326 |
rs528889376 | in-del | -/A | 0.00795532 | 0.062565 | intron-variant | RFWD2 | GRCh38.p7 | 1:176022399 | AAAGCAATGTTTAAG[-/A]AAAGTACAGCCCATT | 64326 |
rs528894864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176192627 | TTTGCTCACATTTCA[A/G]AAGAGTACCCAATCA | 64326 |
rs528912746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176199775 | TGTTAGGTGTGAAGG[C/T]AGACACAGAGTATGA | 64326 |
rs528917566 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176019879 | AAAAAAAATCACTAA[C/T]GGCGTTACAGGAAAC | 64326 |
rs528919495 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176004563 | GTTTTTAGCATGAAG[C/G]GTTGTTGCATTTTGT | 64326 |
rs528934503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176167037 | CACTCAGCTTAAGTG[C/T]TTCCTCATCAAGGGG | 64326 |
rs528963596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176117437 | ATCTTTTACTTCCTC[C/T]ATCTTAGCATTTCTA | 64326 |
rs528979846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176020550 | AGGCGAGGTAGTGCA[C/T]GCCTGTAATCCCAGC | 64326 |
rs528980605 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176171471 | ACTAAACTTTCTCCA[-/T]TATCAGCAATAAGCG | 64326 |
rs528987862 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176206153 | CGAGGAAGCTTAGTC[C/G]TCTCCATTTGCAAAT | 64326 |
rs528993320 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176070228 | CAAATCAATCACGAA[C/G]TTCTGGCTACCCTAG | 64326 |
rs529010614 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176049580 | AAACAGGTCCCCCCC[A/C]TCAAACCACCTTTTT | 64326 |
rs529029142 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176015825 | TGATGACAAGAACAC[-/T]TTTAAGTGGAATTAT | 64326 |
rs529046689 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175955899 | AGACCAGAGACTCAA[C/T]AGTGTCACAATGCCA | 64326 |
rs529049721 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176140608 | GGAAAGAAGAAATGG[G/T]CTAAATTCACTCTGT | 64326 |
rs529054614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176180159 | TATTTGGTCATTAAA[C/T]GCAAGGATTTGTTTT | 64326 |
rs529074591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176139706 | AAGTGAATTAATGAA[A/G]TAAGAGAAAACCAAA | 64326 |
rs529075706 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175968291 | TCAGACGGATACAGA[C/G]GTAACTTTACTTGGT | 64326 |
rs529098354 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176067398 | CTGCACCTATAAAAA[C/T]TCCGACACCCTAGTG | 64326 |
rs529107929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176091274 | ACCCAGGAGGCAGAG[A/G]TTGCAGAGAGCTGAG | 64326 |
rs529152002 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175967746 | TTGGAGAAATCACTT[A/T]CTTAATGAGAAAATC | 64326 |
rs529166580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176193148 | TTAAAGAGTAATAAA[C/T]GAATGGCCAACAAGC | 64326 |
rs529167752 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176056471 | CTTACAATTAGACTT[A/C]AACTTCAGTGCAGAC | 64326 |
rs529169153 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176013936 | AAAGATTACTCAGCC[A/C]GATTTTATAATCATT | 64326 |
rs529169455 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176037259 | TACAAAAACAAAAAT[C/T]AGCCAGGCATGGTGG | 64326 |
rs529169929 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:175973139 | TCTGGCCAAGCCTTA[-/T]TTTTTTTAACACTTT | 64326 |
rs529188233 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176146728 | CTACTCTGAATCAAA[A/C]TTCTAGACTCAATAT | 64326 |
rs529194100 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175992150 | TTTTGATACAGGCAT[A/G]CAATGCATAATAATC | 64326 |
rs529207100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175974811 | GCTGAGGCAGGTGGA[C/T]CACCTGAGGTCAGGA | 64326 |
rs529226798 | in-del | -/TC | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176127201 | ACCTCAAATATTTCT[-/TC]TGAGAACATTTAAAA | 64326 |
rs529230997 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176186455 | CTGAGGAAGAATGAT[A/C]ACTTGAGCACAGCAG | 64326 |
rs529239431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176098646 | CGTACTCTTAAGGAA[C/T]TAATCTGCTCTTTAG | 64326 |
rs529262848 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176136703 | GGATAACCATCAACA[A/C]AATATAGCTAGAAGT | 64326 |
rs529278867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176145336 | TAAACTGGAAAAAAA[A/G]TCTACTGGTATCACA | 64326 |
rs529282624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175966837 | AGAGGAAAAGGCTTG[A/G]CCACAGAACCAAAGT | 64326 |
rs529295945 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176124890 | TTCCCACCAGCACCA[C/T]ACAAGGGTTCCCTTT | 64326 |
rs529299289 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176067504 | GGCAGGCCATCAACC[A/G]GCAGGAGGATGCAGA | 64326 |
rs529302557 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176157774 | ATTAAGAAACAAGCA[C/T]GCAAAGAAGCAGAAA | 64326 |
rs529312147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176097242 | GAAAAAAAAACGACT[A/G]AATTATTTTTCTCCA | 64326 |
rs529333151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176088717 | AAATATCTATTTGGC[C/T]GGGCGCAGTGGCTCG | 64326 |
rs529351031 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176066418 | TCCTCTCCTAAATAG[A/T]AAAGTGAACTCCTAC | 64326 |
rs529355719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176006579 | CATTTGCTGGTCTGT[A/G]AAGTATTTTATTTCT | 64326 |
rs529370223 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176198206 | ACTTTGAAATAAAGG[A/C]TAAAAATTACACTAC | 64326 |
rs529370818 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | RFWD2 | GRCh38.p7 | 1:176151330 | GAAAGAAGGAAAGAA[A/G]GAAAGAAGGAAGGAA | 64326 |
rs529373774 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176103892 | CAGTTCCAATAAAAA[A/T]TACCAAGAAGCTTTT | 64326 |
rs529402320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176096796 | TGTAGCCAATCTGGT[C/T]TGCTTTACATAACTT | 64326 |
rs529402435 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176124043 | TTTGGCTTCTTCACA[C/T]CTCAGATTTCAGAAT | 64326 |
rs529407146 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176064497 | CACTGAACACAGTAA[C/T]GTGAATAGCCCTATC | 64326 |
rs529408945 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176197250 | GACCCTCATCTCTAT[C/T]AAAAACTTATAAAAA | 64326 |
rs529410022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176152036 | ATTGTTGGCTGCAAA[A/G]TCCTAGCACTGCGGG | 64326 |
rs529429472 | in-del | -/AAC | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176060394 | TCTAGTAGAGAAAAT[-/AAC]AAGAGCTGAAAAAGA | 64326 |
rs529440299 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992461 | TGCCTCACTCGGGAA[-/G]CGCAAGGGGTCAGGG | 64326 |
rs529450603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176184300 | GTTCTCCAACCTATC[C/T]CCACAAGTGAGTAAT | 64326 |
rs529452651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176166347 | GCCCAGGCTGATCTT[A/G]AACTCTTGGCCTCGA | 64326 |
rs529482061 | snp | A/C | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992713 | GCACCTGCCATTGCC[A/C]AGGCTTGCTTAGGTA | 64326 |
rs529495657 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175952372 | GGTTGCAGTGAGCCA[A/C]GATGGCACCATTGCA | 64326 |
rs529495708 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176075985 | TCCAGCCTGGGTAAC[A/G]AGCGCAAAACTCCAT | 64326 |
rs529507077 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176035266 | AACTATTTTTTTTTT[A/T]AAAAGAATCAAATGA | 64326 |
rs529536479 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175985450 | ATTCAATTTCAGAGA[C/T]TGATATGAAGTTCAG | 64326 |
rs529553404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176089363 | CAGATTAAGAGGCAA[C/T]AATATACACATGCCA | 64326 |
rs529556805 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176130503 | GTCATTGGTTTGATT[A/C]ATTCTACGGAAAGTC | 64326 |
rs529571373 | in-del | -/CA | 0.0111196 | 0.0737302 | intron-variant | RFWD2 | GRCh38.p7 | 1:176054357 | GTAGAGACAGGGTTT[-/CA]CACCATGTTGGCCAG | 64326 |
rs529576731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176178693 | CCCGTCTCTACTAAA[C/T]ATACAAAAAATTAGC | 64326 |
rs529620072 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176141960 | GCTGGTCTTGAACTC[C/T]TGGCCCTCAAATGAT | 64326 |
rs529635047 | snp | A/C | 0.0547245 | 0.156101 | intron-variant | RFWD2 | GRCh38.p7 | 1:175996022 | TGGCAAAACGAATCC[A/C]GCAGCACATCAAAAA | 64326 |
rs529641780 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176179220 | GCTTGACCCTGGGGG[A/G]CAGAGGTTGCAGTGA | 64326 |
rs529650145 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176154124 | ATACTTAGGGAGGAG[C/T]GCCTCTTCCTCAATT | 64326 |
rs529653329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176133611 | ATCCAACACCTAGAA[C/T]AGTCCCTAGCACATC | 64326 |
rs529665760 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176005046 | CCTGTTATTGGTCTA[C/T]TCAGAGATTCAATTT | 64326 |
rs529667248 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176175189 | GCCCTCAATATTCAA[A/C]AAACCTGAGTTCCCG | 64326 |
rs529670524 | snp | C/T | 0.00160417 | 0.0282756 | intron-variant | RFWD2 | GRCh38.p7 | 1:176052189 | GATACACAAATACCA[C/T]TGTGTTAAAGCTACC | 64326 |
rs529674548 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175965675 | CTCACTGCAACCTCC[A/G]CTTCCCGGGTTCAAG | 64326 |
rs529698490 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176037253 | TAAAAATACAAAAAC[A/G]AAAATTAGCCAGGCA | 64326 |
rs529707320 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176143672 | TATATAAGGGGTGCA[A/G]GTAGGGGGACCAATT | 64326 |
rs529712570 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176086414 | TGAATTTTTAGTAGA[C/G]ACAGGGTTTCACCGT | 64326 |
rs529734082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175964056 | TTAGTACTTTCCATG[C/T]ATTTTCTAATTTTAT | 64326 |
rs529735833 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176100346 | GTGAGCCAAGATAGC[A/G]CCATTGCACTCCAGC | 64326 |
rs529738716 | in-del | -/T | | | intron-variant, utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175967875 | AATATTTCTTTTTTC[-/T]TTTTTTTTTTGAGAT | 64326 |
rs529749540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176004694 | GCCTTGCATCCCAGG[A/G]ATGAAGCCCACTTGA | 64326 |
rs529752912 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176008471 | TATTTGTTTTTATTT[C/T]TTTTTGTTAATATTC | 64326 |
rs529754820 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176122094 | GAAGTAAGCCGAGAT[C/T]GCGCCACTGCACTCC | 64326 |
rs529772184 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176187805 | TACACCAAAAAGAGA[A/C]AATACGGGAAAATAT | 64326 |
rs529773405 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176101136 | TAAGAGTGAATACTC[C/G]CACCCTGTAGCATGC | 64326 |
rs529789372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176188382 | AATGAAATACCATTA[A/G]TTCTTTCCAATTTTG | 64326 |
rs529791888 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176204165 | AAATCTGAGTTCTCA[-/T]TTTTGTCCTTACCTG | 64326 |
rs529798715 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176152733 | GCGTGAGCCACTGTG[C/T]CCAGCTTAAAATTCT | 64326 |
rs529810386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176120769 | ACCATAATGAAGAGG[C/T]AGCCAAGAGAAAACA | 64326 |
rs529831264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176093484 | GTGGCTGAGGTGGGC[A/G]GATTACAAGGTCAAG | 64326 |
rs529838493 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176148814 | TTCAGCACATCTCCA[C/G]AAAATGATTTTTTAA | 64326 |
rs529855750 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176014173 | AAGAAAACAGAAAGT[A/G]AGAGAATACATCTGA | 64326 |
rs529859979 | snp | A/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176208647 | AAGGTTTTTAAAATT[A/T]AAAAAAAAATGAGAA | 64326 |
rs529880815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176121602 | AGCTGGAATACTACT[C/T]TGACAGTTGCAACTT | 64326 |
rs529892849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175986113 | CAAGCTCTGCCTCGC[A/G]GGTTGATGCCATTCT | 64326 |
rs529904837 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176086798 | AAGAGCCCACATTGC[A/C]AAGACAATCCTAAGC | 64326 |
rs529907845 | in-del | -/CTAAA | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176066815 | CCTTTGTTCTGGTCT[-/CTAAA]CTAGAGTTTCTCTAT | 64326 |
rs529914886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176037999 | ATGAAAAAGTATTTA[C/T]GTTTCTATTTGCAGA | 64326 |
rs529920329 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176205115 | TTACACGGAGGCTAA[C/G]ATGTTTGTGTTCGTT | 64326 |
rs529922018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176126946 | ATCAAAAAGTCTATT[C/T]ACACCAAAATTTAAA | 64326 |
rs529923578 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176000089 | TTGACTGTTGCCTTC[A/G]CTGTGCAGAAGCTTT | 64326 |
rs529928716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175984431 | GCCTAGATTTCAGAG[A/G]ATGTATGGAAACGCC | 64326 |
rs529933174 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176172322 | GTTAGGATTATAGGT[C/T]TGAGCCACTGCACCT | 64326 |
rs529982547 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175975461 | GTCACCCAGGCTGGA[A/G]TGCAGTGCCACGATC | 64326 |
rs529983306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175994341 | ACTGCATCAACTAAC[A/G]AGCAAAATAACCAGT | 64326 |
rs529987391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176079585 | CCCAAGCCTCAGTGT[C/T]GTGCAATATACCCAT | 64326 |
rs529997423 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175993509 | GAAAAAAATTTAGAC[A/G]AATGTATAACTAGAA | 64326 |
rs530024131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176036766 | GTTATTTTGCTTAAT[C/T]GTAGGCCAATGTAAA | 64326 |
rs530029101 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175948675 | AATGTGCATCTTGTT[A/C]CTAATGGCATACAAG | 64326 |
rs530043657 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176176418 | AAACAGAAAACTCAA[C/T]GAAAGACAAAAATTA | 64326 |
rs530045986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176170011 | CATCTCAAGAAACCA[C/T]TTTCTTTGTTCATCC | 64326 |
rs530054440 | in-del | -/AT/T | 0.227424 | 0.250118 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176208462 | TCTCAAAAAAAAAAA[-/AT/T]TTTTTTTCATTTGCC | 64326 |
rs530058855 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175988627 | CACCTGAGGTCTGGA[C/G]TTCGAGACCAGCCTG | 64326 |
rs530070565 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176125555 | GTGTGGATTTGTTTC[A/G]GGGTCCTCTATTCGG | 64326 |
rs530094900 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175945999 | AACCTATGTAGTTTT[C/G]AGCTCTTGTAGGTAT | 64326 |
rs530096997 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176168372 | TACAAATTTTATATA[G/T]AGAGAGAAAGGTAGA | 64326 |
rs530099651 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176028880 | CTCCCCACTCAGCCT[C/G]CCGGGTAGCTAGGTG | 64326 |
rs530134233 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207499 | GGTATAGGTGGTGGG[A/G]TGGTTTGAAAGACGG | 64326 |
rs530142058 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176010228 | CAAACATCAGGATAT[C/T]TGACTTTTAAAAACT | 64326 |
rs530148781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176119396 | AAATGAATGATATTG[A/G]TATCTCAGTGTATAC | 64326 |
rs530150321 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176132566 | ATATACACATATGTA[C/T]GTATATATACTATAT | 64326 |
rs530159956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176174366 | GGTTTCCCTATTATC[C/T]AAACTAGGCCATCAA | 64326 |
rs530164001 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176077823 | AGAATACAAAATCGA[C/T]GTACAAAACTTGGTA | 64326 |
rs530175971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176002445 | GTGCCATGCTGGTGT[A/G]CTGCACCCACTAACT | 64326 |
rs530179751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176036080 | AAGCAAATATACTAG[C/T]CATGAAAATAATATA | 64326 |
rs530185571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176201595 | TAGTAATGAACTACT[A/G]TTGCACAAGTACCTT | 64326 |
rs530215987 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175968970 | GACAAGTATGAGGGG[A/G]AAAAAATGACTGGAT | 64326 |
rs530218415 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176180964 | TAACTTGTAATGAAG[C/T]GAAATAGTAAATCAG | 64326 |
rs530223194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175983563 | ATACAGAAAATTGGT[A/G]CCAGAAGTGGGGTGC | 64326 |
rs530223517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175975720 | GGCCAACCCTTTTCT[C/T]TATATTCCTAAAATA | 64326 |
rs530227860 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176065216 | TCTGTTTAGGTCAAG[G/T]GTTAGTATGTTATGG | 64326 |
rs530238270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176134195 | GTAGAACTGGACTTC[C/T]TGATAGTACACATTA | 64326 |
rs530240860 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176018486 | TAAAGAAGAGCTGCT[C/G]AGCTTAAAGCACAAG | 64326 |
rs530243398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176194738 | ATATTAAAACACGTA[C/T]ATAATAGACATGAAG | 64326 |
rs530257498 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176198416 | ATGATGTTATAATAT[G/T]AATGAAGCCTTCAAC | 64326 |
rs530262555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176057676 | CAGTGGCGTGATCTC[A/G]GCTCGCTACAACCTC | 64326 |
rs530263955 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175998681 | ACAGATAGTTCATAA[G/T]GTACAATAGTCCAGA | 64326 |
rs530280671 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176158944 | CTGTGCCTGGCCTAA[A/G]GTTCTTGTAATACAG | 64326 |
rs530299771 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176071862 | TTTGTGGATATGTGT[A/G]AAATTATTTCAGCTT | 64326 |
rs530317134 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175969282 | CATTGTTAGGGACCA[A/G]AACACACTACCTCCA | 64326 |
rs530318608 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207874 | AAGTTAAGATGAAGT[C/T]AGTGAAGTTTTCTGC | 64326 |
rs530325385 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175972290 | GAAAAATACTAATAC[A/G]CATGTTGAAACTATC | 64326 |
rs530340150 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175948298 | AAGGGCTCTGGAACT[C/T]GGATGTGTTGGAGTC | 64326 |
rs530353331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176008089 | AGCGCAGTATTTGGG[C/T]GGGAGTGACCCGATT | 64326 |
rs530355907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176148175 | TAGCAACAGTTGAGA[A/G]TAAGAAAAATCTAGT | 64326 |
rs530371756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176161989 | TTATCAAAAAACATA[C/T]ATATAAACCAAGAGT | 64326 |
rs530376351 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176022483 | AGTATGATTCTGTAT[A/C/T]GCTCTCAGTGGTAAA | 64326 |
rs530405097 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176025390 | CTACTAGACTTAATG[C/T]AAAAAATTTATAAGG | 64326 |
rs530422586 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176162175 | GGTTCTAATCTTCTC[-/A]AAAGTTTGGTGGTTC | 64326 |
rs530446882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176015016 | AGAGAGGAAAGGTAA[C/T]GACTGGGTGAGTCTC | 64326 |
rs530455392 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176196929 | AGAAAGAAAGAAAGA[A/G]TGAAACCAGCAGGAG | 64326 |
rs530460627 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176204645 | TGAAATACTCAGGAC[C/G]ACGGTGGCTCACACC | 64326 |
rs530473352 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175959259 | ATATACTTTAGCATT[A/C]ATTTATGGTAAGAAC | 64326 |
rs530475575 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175950370 | ATTTAGAATTAAACT[A/C]TCAGATAGCTAGATA | 64326 |
rs530478205 | snp | A/G | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992274 | AGGTGGAGGCAAGAT[A/G]GCCAAATAGGAACAG | 64326 |
rs530487652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176171158 | AAAAAAGTAGGCTGT[C/T]ATATCTACACTGAAA | 64326 |
rs530492320 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176032472 | ACAGCAAACATATAC[C/T]ATCTCACACAGTTTT | 64326 |
rs530504500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176033100 | TCACTTGTGCATTAA[C/T]TTATGCAACTAAGAA | 64326 |
rs530515777 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176008957 | TGTATGTTGTGGAAT[C/G]CTTTCAGAGCTTAAA | 64326 |
rs530525463 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176146720 | GCACCCAGCTACTCT[C/G]AATCAAAATTCTAGA | 64326 |
rs530525807 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175986112 | GCAAGCTCTGCCTCG[C/T]GGGTTGATGCCATTC | 64326 |
rs530540722 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175986260 | TCCTGACCTCGTGAT[C/T]TGCCCGCCTCGGCCT | 64326 |
rs530549909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176171721 | ATAAAGTGCAATAAA[A/G]CAAAGTACAATAAAA | 64326 |
rs530557142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176170548 | AATCTTTTTTTCTAA[A/G]CAGTAGGTCTCAACA | 64326 |
rs530569366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176025975 | CACAATAATGCCAAT[A/G]GTTCTAAAATCAGCA | 64326 |
rs530585171 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175985764 | ATTTGGTCCTTTTTT[C/T]CTAATTTTACTTGGA | 64326 |
rs530607209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175980816 | GTGAGTAGCTAAGTA[C/T]GTATGTTACGGTTCA | 64326 |
rs530612471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175973224 | CTGGAGTCTGAATTA[C/T]ACAAATGTCTCATGA | 64326 |
rs530614671 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176153743 | CACAGATGGCCCTTA[C/T]TATTTTGCGGTATGT | 64326 |
rs530616858 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176117826 | CTTGAACTTGTGAGA[C/T]GGAGGTTGCAGTGAG | 64326 |
rs530625031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175973736 | TAGATCAATCTAATG[A/G]TATTTATCTACCCAA | 64326 |
rs530627535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176089120 | AGCCTGGCCAAGATG[A/G]TGAAACCCCGTCTCT | 64326 |
rs530640472 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176191635 | TTTACACCTATACCG[A/G]TAACACTAGATCCTC | 64326 |
rs530662750 | in-del | -/AAAT | 0.00676609 | 0.0577691 | intron-variant | RFWD2 | GRCh38.p7 | 1:175951251 | AAAACTCCATCTCAA[-/AAAT]AAATAAATAAATAAA | 64326 |
rs530664010 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175995375 | TCAAAAGCTAGCAGA[A/G]GGCAAAAAATAATTA | 64326 |
rs530665016 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176050773 | ACCTTACATAAATTA[C/T]ACAAGCTTCAAATCT | 64326 |
rs530690470 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176068199 | ATTTCTTATTAGAAA[G/T]GTCTTCCTTCCTTCC | 64326 |
rs530700082 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176026107 | ACTAAGAAATGTATG[A/G]AAATGTATAATACTG | 64326 |
rs530703300 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176121696 | CAAAATCCAACTGAA[A/T]ATTAAAATGAAATCT | 64326 |
rs530710329 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176093892 | GCTGGGCATGGTGGC[A/G]CACACCTGTAGTCCC | 64326 |
rs530721913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176152161 | CTGGGCATAGTGGCA[C/T]GTGCCTACGGTCCCA | 64326 |
rs530724511 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176061130 | CAGATCAATACAACA[C/G]AACAGACAGTTAAGT | 64326 |
rs530725593 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176069163 | GCACTCCAGCCTGAG[C/T]AACAGGGTGAGACCT | 64326 |
rs530731516 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176061657 | AAAAGAAAAAGAAAA[A/T]ATGAAACTAAACCAT | 64326 |
rs530759184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176145382 | AGTGCAACAGAAATG[C/T]TCATACAATGCCTAT | 64326 |
rs530767555 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176118588 | GACAAAATAGTAAGA[C/T]TCCGTTTTCTACATA | 64326 |
rs530777743 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176019154 | TTGGGCAACAGAGCG[A/G]GAATAGACTTTTTAA | 64326 |
rs530778871 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175991605 | TATAAACTTAAAAAA[A/T]TTTTAAAGCTTTTTG | 64326 |
rs530787448 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176166140 | ATTTTATTTATTTAT[G/T]TATTGAGACAGGGTG | 64326 |
rs530806538 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176059607 | CCTGCCTCAGCCTCC[G/T]GAGTAGCTGAGATTA | 64326 |
rs530811790 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175972089 | TAGGATACTTAACAA[A/G]ACAAAAGGAGAGAAT | 64326 |
rs530821721 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176116324 | AGGTCAAGGCTACAG[A/C]ATTCCAGCCTGCGTG | 64326 |
rs530835809 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176151402 | AAGAAAGAAAGAAAG[A/G]AAGAAAGAAAGAAAG | 64326 |
rs530842449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176019737 | ATCGTAGCATGCTCC[C/T]GTAGTCTCAGCTACT | 64326 |
rs530845951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176009471 | TATGTGAAAGGCATA[C/T]AAGTAAAGGTTAAAT | 64326 |
rs530849699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176159258 | GACACAAAATATGAA[C/T]AGGTAATTCATCAAA | 64326 |
rs530856636 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176071710 | ACTGCTGACTACAAA[G/T]ATCTTCCTTATATTA | 64326 |
rs530865752 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176016944 | GTGTTGAAGCTAATC[A/T]AAAGTATGCACTAAC | 64326 |
rs530873584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176024556 | TGTGAAGGACTAAAC[A/G]CTCTTCACGTATGAT | 64326 |
rs530875297 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176016628 | AAATGCAGACGGAAC[A/G]GAGATGCCAGGTACA | 64326 |
rs530877944 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:176196083 | AAATGAGAAGTATTA[G/T]GAACTGATTGAAAAT | 64326 |
rs530877955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176203808 | AACTTACTTTCAAAT[A/G]TAAGTCAGGAGAGGC | 64326 |
rs530918754 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176156844 | ACAAAAGTAGACAAT[A/T]ATAATAATAACAGTA | 64326 |
rs530935716 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176013304 | TAAGAAAAGAAAATA[C/T]GGTTCAGAAATTTAC | 64326 |
rs530935870 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176101787 | AAATGGTCATGCAAC[C/T]GAAGCCTCAGATGAT | 64326 |
rs530949698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176189358 | TCTGGCTTGCTTTCA[C/T]TGTTTCTAGGGACAG | 64326 |
rs530969608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176060164 | AGATCTTGCTTTAAA[A/G]CAACTACTTTAAAAA | 64326 |
rs530975456 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175982441 | TCTCCTCCTTCTCAG[A/C]CTACTCCATGTGAAG | 64326 |
rs530976068 | snp | C/T | | | intron-variant, nc-transcript-variant, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175968515 | TTTTTCATTTGTCCA[C/T]ATGGCTGGTTCCAGC | 64326 |
rs530978064 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176153272 | CTTATACATGTCCCT[A/G]GGGTATAAAATTCTC | 64326 |
rs530995532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176073719 | GAGATACTGTCAAAG[C/T]AAACAAATGCTGCCA | 64326 |
rs531009024 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176066338 | GTGCCTTTTCTCCTG[C/T]CAATTTGTTGTCAAC | 64326 |
rs531012814 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176039404 | AAACTAGGAAAATAA[C/G]AGCAAGTTAAATCTA | 64326 |
rs531012956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176177176 | ATAAAAATAAACTAC[C/T]CATAGTTATTGCTAG | 64326 |
rs531034356 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176066797 | AGAAAAACAAAGATA[G/T]TTCCTTTGTTCTGGT | 64326 |
rs531055630 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176051272 | GGATACTAACATAGC[C/T]GCTGAAAAAACCAAG | 64326 |
rs531057184 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176128983 | TCCCTGTCCTCCATA[A/T]CCCTCCCAAGCATAT | 64326 |
rs531075539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175965261 | TTCAAATAAATTTGC[C/T]CTTCTTTTGATGCAT | 64326 |
rs531101437 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176001273 | TCTATTTCAAAAAAC[C/G]TGGATTCATCGAATG | 64326 |
rs531110319 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176005652 | TCAGTTTCCATGAAG[A/T]TGAGCGGTTTTGAGT | 64326 |
rs531116783 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176125093 | TTTACCCATTTTTAA[A/G]TGATTATTCGATTTT | 64326 |
rs531132225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176143896 | AAATTCTGGAGACTA[C/T]TCAACCCCACTCAGA | 64326 |
rs531135067 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176184094 | CCAAGACTAAAGAAC[C/G]AGAAAAAAATATATA | 64326 |
rs531141786 | in-del | -/A | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176122943 | ATGTCAAAAATAGAC[-/A]AAAAATAAGCTCAAA | 64326 |
rs531145528 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | RFWD2 | GRCh38.p7 | 1:175993869 | GCAAGGCAGGCCAAC[G/T]TTCAGATTCAGGAAA | 64326 |
rs531145750 | in-del | -/T | 0.0174175 | 0.0916809 | intron-variant | RFWD2 | GRCh38.p7 | 1:176189384 | ACAGTATTATGTTTC[-/T]TTTTTCCGTTGGGAA | 64326 |
rs531171227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176200622 | TGTTTCACTTTATAT[A/G]GAAACAGAGGCAAAA | 64326 |
rs531175333 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175958668 | GACTTCCCTCAGAAT[A/G]AGAATAAATAATGTT | 64326 |
rs531183253 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176136287 | CAATAAAACATTGTA[A/G]AACAAATTTAGACTA | 64326 |
rs531193234 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175972486 | TTTTTTTTTTTTTGA[C/G]ACAGAGTCTGGCTGT | 64326 |
rs531228192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176106415 | TGGCAACTAGACAAC[C/T]AACACTGGCCACAAG | 64326 |
rs531233456 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176014623 | AGGGTCCTAAATGAA[A/T]CTTCACCTTACTTAT | 64326 |
rs531239899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176147577 | TACTACAAGAAAATA[C/T]GGTCCAAGAGAAAAG | 64326 |
rs531242758 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176057107 | ACAAACTACCCCTGC[C/G]TTTCCAATATTTGCT | 64326 |
rs531248323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176006085 | TCCTGCTGAATTGAT[C/T]CCTTTACCATTATGT | 64326 |
rs531261119 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176049433 | GAACCTGTAGAGTAT[A/G]TTTTTAAAAATATTT | 64326 |
rs531264031 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176096026 | AGCAGGACTCTCTCT[C/T]GCTTTGCTGAGCGTT | 64326 |
rs531281211 | in-del | -/ACAC | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175966281 | AATTGTGTTTGCAAT[-/ACAC]ACACACACACACACA | 64326 |
rs531316834 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:175974111 | AACAGTGAGATAAAC[-/A]AGTCTAGAACTATTA | 64326 |
rs531321750 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176076847 | TTATGAACATCTCTA[C/T]GCACAGACTAGAAAA | 64326 |
rs531325030 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175974859 | CCAATATGGGTGGTC[A/G]AGGCTGCAATGAGCC | 64326 |
rs531332928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176064141 | ATTTGGCCCATGGTC[C/T]ATAGTTTGCTGATTT | 64326 |
rs531337453 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175975488 | GATCTCGGCTCACTG[A/C]AATCTCTGCCTCCTG | 64326 |
rs531339078 | snp | A/T | 0.00106385 | 0.0230389 | intron-variant, nc-transcript-variant, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175968472 | ATATATTTATGTAGG[A/T]TCGCTGCAATCTGTA | 64326 |
rs531351831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176098765 | TTGGAATTCTATTTC[A/G]TAACATCAAGTGTTT | 64326 |
rs531355989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176193923 | CAACTTTAAAACGGC[A/G]TATTTCAGGGTTGTG | 64326 |
rs531366151 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176007890 | GTTCCAGCTTCCTGG[C/T]TGCTTTGTTTACCTA | 64326 |
rs531384220 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175956269 | TTACAAATGCTGTTG[A/C]AACAACTGCAGGTAT | 64326 |
rs531392719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176160970 | ATCAGGGATTCCAAC[C/T]GCTTCTTAAACAGAT | 64326 |
rs531405275 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176034199 | TACCATTTTTCCCCC[-/T]CTCTTCTCCCTTGGC | 64326 |
rs531410413 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176174448 | CTAAGTTCCTTCTCC[A/C]AGTTTGCCATAAAAC | 64326 |
rs531453288 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176051059 | TAAACACAAAGGGAT[-/A]AAAAAAAAGAATAAG | 64326 |
rs531490234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176133081 | ATGTACGTATATATA[C/T]TATATATACACACAT | 64326 |
rs531496908 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175998759 | TCATTTCTCTTCCCT[C/T]ATACACATTTTTGGT | 64326 |
rs531506924 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176205441 | TCCTAACAGTTCCAA[A/C]TTCTAGCTCTATCTT | 64326 |
rs531507414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176003992 | CCATGAGCATGGAAT[A/G]TTCTTCCATTTGTTT | 64326 |
rs531512644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176085720 | TTCAGCACAAAAACC[C/T]AGAAACAGATCTGAA | 64326 |
rs531521533 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176140638 | TAAACATAACCCCGG[A/G]AAGGAGAACTTAGAA | 64326 |
rs531534719 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176054749 | TCCTGGATCTTTTCC[A/G]TAAGGCTTCCATGTT | 64326 |
rs531561926 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175996117 | TCAATAAATGTAATC[C/T]AGCATATAAACAGAA | 64326 |
rs531581638 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176002516 | CCCCTTCCCCCCCAC[C/T]CCACAACAGTCCCCA | 64326 |
rs531584414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176125634 | TACTATAGCTATATA[A/G]TATAATGTAAAATCA | 64326 |
rs531591275 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176099603 | TATGGCAATATAGTT[C/G]TTTACATCAGTGCAA | 64326 |
rs531593065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176091333 | CCTGGGCAACAGAGC[A/G]AGACTCCGTCTCAAA | 64326 |
rs531597413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176025762 | AGGTGTGGTGGTGCA[C/T]GCCTGTAGTCCCAGC | 64326 |
rs531616360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176090298 | TATGTCTCCTTAAAA[C/T]GTATACCAACCACCT | 64326 |
rs531622469 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176003520 | TCCATCTTGAATTGA[A/T]TTTTGTATAAGGTGT | 64326 |
rs531623587 | snp | C/T | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176185178 | AATCATAACAACTTA[C/T]TAGCTATTTAAATAA | 64326 |
rs531629912 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176082447 | TATGTTATCTGGAGA[C/G/T]ATTAGGTTATCTTGA | 64326 |
rs531664137 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176023223 | CAATAAGAACTACAA[A/C]AGCCTTTCCACACAC | 64326 |
rs531677275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176180800 | AATCAGAACCAGTCA[C/T]TACATCTAATAACCA | 64326 |
rs531684415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176187582 | ATCACAGTTCTACCC[C/T]ACAGCTTTCAAGAAA | 64326 |
rs531691617 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176138593 | ACTGCTCAATTGATA[A/G]AGTCTCTAAAGCCCC | 64326 |
rs531697582 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176161089 | TCAGTTCTTAGCTTT[A/C]TCCCTATTGCTGGTG | 64326 |
rs531710940 | snp | A/G | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:175959739 | GTAAAAATTCACACA[A/G]TACAAAAGAGTAGGG | 64326 |
rs531711717 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175974787 | CCTGTAATCTCAGCA[C/T]TTTGGAAGGCTGAGG | 64326 |
rs531732252 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:176137693 | TTAACTACTATTCTT[G/T]ACTACCTATTGAAAA | 64326 |
rs531737663 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RFWD2 | GRCh38.p7 | 1:175998176 | GGGACATGGATGAAA[C/T]TGGAAATCATCATTC | 64326 |
rs531758556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176117543 | ATCACATGACATACA[C/T]ACCAACCGTATAAAC | 64326 |
rs531758597 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175950716 | CTAAGCTAATAAAAT[A/G]CCCAATATTTTTTTC | 64326 |
rs531760173 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176124936 | TAGCATTTGTTACTG[C/T]CAAACTTTTGGATAA | 64326 |
rs531778978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175952464 | CAAGAAAGCCATCCA[C/T]TGAGATACACAAAAT | 64326 |
rs531798782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175966911 | CAAATTCCCACTCTC[C/T]TTCCAATCTTCCACC | 64326 |
rs531805447 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176067969 | AAGAAACAAGCCACA[A/C]CCCCATCGCACACCC | 64326 |
rs531821239 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176111277 | AAATGCTACCTAATT[A/C]TTTAATTTATTTTTA | 64326 |
rs531833457 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176002170 | TCATTTCTACAAATA[G/T]TTTCTACCTCTTTCT | 64326 |
rs531837568 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176133934 | CACAGACCAAGTCAT[C/T]CTCAAATGTTTCAAA | 64326 |
rs531851492 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176136245 | CTGAGCGATTTTTTT[G/T]GTCAGTCTAATCGAG | 64326 |
rs531860466 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:175996570 | GGATACAAAATCAAT[A/G]TACAAAAATCACAAG | 64326 |
rs531870750 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176146227 | AGACTGGCTTTTACA[C/T]GGAACCCAACACCCT | 64326 |
rs531873568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176185580 | GAGAACAAAAATGCA[A/G]AACCTTGTAAAAAGA | 64326 |
rs531878476 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176135355 | GAAGCCACCACATGC[-/A]AAAAAAAGATAAATG | 64326 |
rs531885655 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175987918 | CAGATAGGGGAAAAT[A/G]AATATCAAGCTTAAG | 64326 |
rs531917137 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176081502 | TGTCTCTTTCCACTG[C/T]GAATTCTCACTTTTT | 64326 |
rs531920397 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992775 | GAGCCCACCACAGCT[C/G]AAGGAGGCCTGCCTG | 64326 |
rs531935954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176167728 | GAACAGTACAGTAAA[A/G]GCACAGATGCTTGAG | 64326 |
rs531946176 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176158292 | GGAATTTTATACTTA[C/T]ATGGAGTACCTTTCA | 64326 |
rs531947717 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175981740 | GGAGAAAATATTTGC[A/C]AACTATTTATCAGTT | 64326 |
rs531959301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175965124 | TCAGGGTGGGCTGTT[A/G]CTATTTGTACTGCAA | 64326 |
rs531959393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176084173 | TATGAAAGGGTTAAC[A/G]TGAACTCTACCAGTC | 64326 |
rs531963026 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176087436 | AACCCCATCAAAAAG[C/T]GGGAGAAGGGTATGA | 64326 |
rs531968286 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207084 | TCCTGAGGACGCCCG[A/C]CGAGCCGGAGGTGGG | 64326 |
rs531985289 | in-del | -/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176108725 | TTTGCAAAAATTGAG[-/T]TATTATTTCATGTGA | 64326 |
rs531994211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175957253 | CCACTCACTCCCTGA[C/T]TCACCGAGAGCAGCT | 64326 |
rs531995794 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:175953161 | CCATTATAAAGTGGT[A/T]TCATATAATCTGAAG | 64326 |
rs531999691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176035327 | AGGAATCATGAGCTA[A/G]AAGACAGAACAATAT | 64326 |
rs532008948 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176173099 | GGGTGATCACGAGGT[C/G]AGGAGTTTGAGACCA | 64326 |
rs532032615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176094262 | TTATTCAAAACCCTA[A/G]AGTAAATCCTTTACT | 64326 |
rs532050326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176084698 | TTCAGAGGAAAAATG[C/T]TTTGTAAATCTAATA | 64326 |
rs532053367 | snp | G/T | 1.6857e-05 | 0.00290314 | utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175945146 | CAATTTGACTTGAGT[G/T]AACCCTTCATACCAA | 64326 |
rs532060056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176127770 | TTCCCAGTAATGGGA[C/T]TGCAGGATCGTATGG | 64326 |
rs532060511 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176051549 | TATACTATACATTTA[C/T]CATTACTTTAGTGTA | 64326 |
rs532061456 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176084063 | TGACTTAAAGATTAC[C/T]AATAATAGCCTACCC | 64326 |
rs532075698 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175964164 | TTTCCCAAAGTCTTA[C/G]AGCTAATACTTAATG | 64326 |
rs532078456 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176076378 | CTGAATAACTCTTGG[A/T]TGAACAAAGAAATTA | 64326 |
rs532089003 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176126843 | TTATCAAGAACCCAA[A/G]GATATTTTATAGAAA | 64326 |
rs532099090 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176005126 | TATTTCTAGATTTTC[A/T]AGTTTATTTGTGTAG | 64326 |
rs532104158 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176134835 | CTAACTCTTCCTGGC[A/C]TGAAATCCAACGCAT | 64326 |
rs532110663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176000116 | CTTTTTAACTTGATA[C/T]GATCCCATTTGTCCA | 64326 |
rs532117293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176095139 | TGGAAAACTATCATT[A/G]TTTACACAATAAGTA | 64326 |
rs532137857 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:175991689 | GTATTTCCTTTTTAC[A/G]TTTCCTTATAAGTTA | 64326 |
rs532156078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176182436 | CCAAGGGGTATCTGC[A/G]ATGTCTAGAGACATT | 64326 |
rs532177109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175957931 | GCAAAAAATTACATA[C/T]TGTATCATTCCTGTT | 64326 |
rs532184404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176024582 | ATGATAAAAAGTTTT[C/T]CATACTTTTACCACT | 64326 |
rs532185118 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176115256 | GAGTTTGAGACCAGC[A/C]TGGCCAACATGGTGA | 64326 |
rs532187515 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176101714 | CCACTTATTTTGTTT[G/T]GATACATGTTTTCTA | 64326 |
rs532198032 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176088156 | AACACCTAATGTAAA[C/T]GACGAGTTAACGGGT | 64326 |
rs532200503 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176174541 | TTCTGCTATGTAATC[C/T]TCCAGCGATTTTCCT | 64326 |
rs532221578 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:175981692 | TCCTCACAACAAAGG[A/C]AACAACAGAGTGAAA | 64326 |
rs532237433 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176005466 | CAATTTTGGATCTTT[C/T]CTGCTTTCTCTTGTG | 64326 |
rs532266705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176142911 | ACATTAGAAAAAATA[A/G]TCTGCATAATAATAT | 64326 |
rs532272870 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176080418 | AATAAAAATAATTAA[C/G]AGCAAAGATTAATGA | 64326 |
rs532278855 | snp | G/T | 1.71773e-05 | 0.00293059 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176176055 | TAAATCAATGAAAAA[G/T]TAATAAACTGGTCAC | 64326 |
rs532286678 | snp | G/T | | | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176208816 | AGGTGCGGTGGCTGA[G/T]GCCCATAATTCCAAC | 64326 |
rs532310039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176122347 | CAGTTTTATACGATA[C/T]ATGGCATATGTACTC | 64326 |
rs532315061 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175962574 | GAGATATCCCCCACT[A/G]TTCCAACCCACCCCT | 64326 |
rs532321503 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176032344 | TTTAATACTGTTTAC[C/G]AAATATAAATAAGCT | 64326 |
rs532324499 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176074378 | GAGAGTTTTTCACAC[C/T]TTCATTTCTTTGGCC | 64326 |
rs532333123 | in-del | -/T | 0.233373 | 0.249446 | intron-variant | RFWD2 | GRCh38.p7 | 1:176084851 | AATAAAATACCAGAC[-/T]TTTTTTTTTCCCCCT | 64326 |
rs532340400 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176164849 | AACTGATTTTTTTTT[A/T]AAAAAGGGAAACTAC | 64326 |
rs532352919 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176143974 | TGAGTGATAAAAAGT[A/G]CCTACAAAAAACCTA | 64326 |
rs532358698 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175985512 | TTCCCCTATAATATA[C/T]CCCTGTGGGGACTTA | 64326 |
rs532363108 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176072395 | TAAGGCCCCTGCCTA[C/G]ATGAATCTCTCAGCC | 64326 |
rs532364739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176169847 | CCTGCAATGTTACAT[A/G]ATAGCATCTTTCTCA | 64326 |
rs532364865 | snp | A/C | 8.46475e-05 | 0.00650512 | intron-variant | RFWD2 | GRCh38.p7 | 1:176162833 | TGCAATAAAGTTCAT[A/C]ATTTAAAATTTTTTT | 64326 |
rs532374038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176067541 | CTGGGACGGTTGGAA[A/G]AGAGCCTGGCCACTG | 64326 |
rs532375482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176025204 | GATATTCTAAACAGC[A/G]GAACACTAAAGCTCA | 64326 |
rs532378253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176030207 | AATAAGCATGATGTA[C/T]TATTTCAATCAAAAT | 64326 |
rs532385973 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176102279 | TTTCCTTTTCGCCCA[A/G]TAAATTACGTTTTCC | 64326 |
rs532405568 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176051864 | GGATATATTTTTGTA[G/T]AGTTGTTCAATGTGT | 64326 |
rs532405940 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176018614 | TGAAAAGAACTGATT[C/T]TGTTTATCAATAGGG | 64326 |
rs532410522 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175946572 | GAAAGTTCACTGCTT[A/T]TCTCAGGATTTATTT | 64326 |
rs532416868 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175983597 | TGAAAAGATACCCCA[A/T]AATGTGGAACTGACT | 64326 |
rs532433593 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:176037131 | GAATAGGCCAGGCGC[A/G]GTGGCTCAAGCCTGT | 64326 |
rs532439609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176168485 | AAGGGAGGAAGGCAG[A/G]AAGGGAGGGAAGAAG | 64326 |
rs532441456 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175946846 | ATATCTTGCATCTCC[C/T]GCTATATTTTGGGCT | 64326 |
rs532480522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176164437 | CCACCCCAACCCCAT[A/G]TATTACTTTGACTAA | 64326 |
rs532482432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176170997 | GGGCTTGGTGGTGGG[C/T]GCCTGTAATCCCAGC | 64326 |
rs532485921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175947618 | CAGGTGATCTGCCCA[C/T]CTCGGCCTCCCAAAG | 64326 |
rs532487041 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176126068 | TGTATGTTGACTTTG[C/T]ATCCTGCAACTTCAC | 64326 |
rs532503326 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176078628 | AATTGCAAAAAAAAA[A/C]ACAAAAATTGACAAG | 64326 |
rs532524193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176120102 | AGAAAAATGAAAAAC[A/G]GTAACCTATAAATAT | 64326 |
rs532529628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176195582 | GGACCATGAAACGAG[C/T]CTCTATAAAAAGGAC | 64326 |
rs532558258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176113108 | CAGTTCTATTTTTAG[C/T]TTTCTGAGGAACCTC | 64326 |
rs532571184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175971129 | ATGCAACAATAATGA[C/T]TCTGGGGTTTTAGAC | 64326 |
rs532573875 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176201739 | GCTGATGCCCCACCA[A/T]CTGATAGTCCACAGG | 64326 |
rs532589736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176195969 | AGATCACTAGCATCA[C/T]GCAATATACCCACGT | 64326 |
rs532591605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176188440 | TAAGGGAAAAACGTA[C/T]CCATTTAGAACCATC | 64326 |
rs532592314 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175955955 | CAATGCAATTCCAAT[A/T]AAAATCATACAAACT | 64326 |
rs532602524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176029738 | AGAAATACTGATACA[A/G]TAACCTGTAGACAGC | 64326 |
rs532613267 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176101179 | ACATCAGTGAAAGCT[C/G]CTTTGACACCCATGG | 64326 |
rs532614059 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176013269 | AGTATGTAACTCATC[C/G]CAAAAATATATGATT | 64326 |
rs532614446 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175972574 | GGTTCAAGCGATTCT[C/T]CTGCCTCAGCTTCCC | 64326 |
rs532652841 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175976135 | TATTGGTAATAAACA[A/G]GGACTCTTATTGAAC | 64326 |
rs532666208 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176194896 | GCCTGAGCACCATGG[C/T]GAGACCCTGTCTCTA | 64326 |
rs532687362 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175976574 | TGAGCCACTGTGCCC[A/G]GCCTCATTTATTCCT | 64326 |
rs532693359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176202392 | TGGGGTTTCGTCATG[C/T]TGCCCAGGATGGTCT | 64326 |
rs532694194 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175976814 | ATTTAGATAGCTCGT[A/T]ATGAAATAAGACATT | 64326 |
rs532730765 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176176980 | TTGAATATTTTACTT[C/T]TAGGAATTTATCCTA | 64326 |
rs532762238 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176159446 | AAATCCACAGAAGAG[C/G]AATCTGTCAATATCA | 64326 |
rs532762415 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176166893 | AGTGAACCATGGTCA[C/G]GCCACTGTACTCCAG | 64326 |
rs532765977 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176151231 | GAAAAAGAATAAAGA[A/G]AAATGTATTTAGAAA | 64326 |
rs532769132 | in-del | -/ACG | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176165418 | TGTGTAGGAGATACA[-/ACG]ATTTAAAATCAATAT | 64326 |
rs532787381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176141989 | ATCCTCCTACCTTCG[C/T]CAACGTGTTAGAATT | 64326 |
rs532787494 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176160873 | TTTCTTACCACCTCC[A/G]TTGGGGGTGGAGGGG | 64326 |
rs532797047 | snp | G/T | 0.00040008 | 0.0141379 | intron-variant | RFWD2 | GRCh38.p7 | 1:176023950 | TTGCTGTCAAAGACA[G/T]AAAATATCATCATAA | 64326 |
rs532809380 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176155238 | TGACTGAAACTAACT[C/T]AAGCAGCGATGAAGC | 64326 |
rs532821569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176198475 | ACTTGAAGTGGATCA[C/T]AACCATAAGAAAACT | 64326 |
rs532837013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176107096 | TTGCCTGTAATCACA[C/T]TGTTCCAGAAATATA | 64326 |
rs532851529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176057748 | TTGCAGCCTCTGCCC[A/G]GCTGCCACCCCATCT | 64326 |
rs532862243 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176148213 | CACATAAAAAATATT[G/T]AGCTATTCAACACTT | 64326 |
rs532871692 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175995854 | TCCTTCTGAAACTAT[A/T]CCAATCAACAGAAAA | 64326 |
rs532887656 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176057703 | CCTCCACCTCCCAGC[A/C]GCCTGCCTTGGCCTC | 64326 |
rs532913111 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176055354 | GCAGGAGAATCGCTT[A/C]AACCCGGGAAGAGGA | 64326 |
rs532917944 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176026702 | GTATAGTGACATGGT[A/T]TAAATTATGCATTTC | 64326 |
rs532918309 | snp | C/T | 2.15408e-05 | 0.00328176 | intron-variant | RFWD2 | GRCh38.p7 | 1:175987124 | AACAAATAATAATAA[C/T]AGTATTTTAGAATAG | 64326 |
rs532919188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176192376 | CAAGTAACAACAGTA[C/T]CAGGCCTCAAACACA | 64326 |
rs532929209 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176116358 | GAGTGTCTCAAAAAA[A/C]CAAAAACAAAAACAA | 64326 |
rs532929834 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176069238 | GTAATACAGTAATAC[A/C/G]TGGTTTTGGACATAA | 64326 |
rs532937130 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176124759 | ACTCTTTCATGTATA[C/T]GTTTCCTTTCTTTTG | 64326 |
rs532940537 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176190000 | AAGAGTAAATAAGCA[C/T]AATGAATAATGATTT | 64326 |
rs532970277 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176110452 | TTGTTCTCTGCCTAG[C/G]AAGTTTTCCCAGGGA | 64326 |
rs532977298 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175974214 | GGTTGGAAATAAGGA[C/T]GGATTCAATATATAT | 64326 |
rs532979832 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176185689 | CCATGAAGACAAAAA[A/C]CTTAAGCTAGGAAGA | 64326 |
rs532992606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176081060 | CTACTTCAGAACCCA[C/T]GCTTTTAATAATAAT | 64326 |
rs533010396 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176146577 | AAGCCCCTGTGACAA[A/T]AAAATTGTTATCTCT | 64326 |
rs533019729 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176059029 | AGCCTTGCTTTGTAA[C/T]ACCAGCACTGCCCTC | 64326 |
rs533025832 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176082290 | GCCCATACATACACA[C/G]ACACACAACTTTTTC | 64326 |
rs533031460 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176123902 | TTTTCTAAAGTAGCA[A/T]CTCTACCACTCCCAA | 64326 |
rs533032468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176020472 | TCACCTGAGGTCAGA[A/G]GTTCGAGTCCAGCCT | 64326 |
rs533045782 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992295 | ATAGGAACAGCTCCA[G/T]TCTACAGCTCCCAGA | 64326 |
rs533046027 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175991549 | AAAGTGTTCTCCCTT[C/T]AGAAATAAATCAACC | 64326 |
rs533052933 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176075890 | CACCTGTAATCCCAG[C/G]TACTGAAGAGGCTGA | 64326 |
rs533073501 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176062576 | TAAAAATCATTTTGG[A/C]AGCTTCTTAAAATGT | 64326 |
rs533083569 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175961354 | ACAGTCGTTTCATTA[C/T]ACAGTAGTGACTTTG | 64326 |
rs533108848 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176004140 | AGTTCACTCATGATT[C/T]GGCTCTCTGTTTGTC | 64326 |
rs533112779 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175981608 | ATAATGGTCTGAAAA[A/T]TTTTTTGGCTAAAAC | 64326 |
rs533115893 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175980492 | TGCACAGTTATAACT[G/T]CATAGAAAGTATTAC | 64326 |
rs533117696 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175955327 | TCAGCAAACTAAGAA[C/T]AGAAAGGAACTTCTT | 64326 |
rs533144983 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176145895 | ACTGCAATCCAAAAA[C/G]GGTGGTCAGGGTGCT | 64326 |
rs533166318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176097964 | ATAAAAGCTGTAGTG[C/T]CTTTCAGTTCACGTG | 64326 |
rs533184109 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176006167 | CAGAGACTAGGATTG[C/T]AACCCCTGCCTTTTT | 64326 |
rs533187417 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176140351 | TACAGACAGAATGCA[A/G]AACAAAATGATATAA | 64326 |
rs533191911 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176048950 | GGCCGAGGCGGGTGG[A/G]TCATGAGGTCAGGAG | 64326 |
rs533191965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176138854 | AACTCCAGCATCCAG[C/T]GATGCTGACCTCTAA | 64326 |
rs533192028 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175953661 | ACGCAAACATTAATC[A/G]TAAGAAAGCTGGAAT | 64326 |
rs533252051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176199125 | GATCGAGACCAACCC[A/G]GCCAACACAGTGAAA | 64326 |
rs533271438 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176031753 | GTTTTATTTCTTTAA[C/T]GTTAATGTGTAAAGT | 64326 |
rs533284909 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176109403 | CCTTTCACCACTGAT[A/C]TACATGACCACCTTT | 64326 |
rs533293714 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | RFWD2 | GRCh38.p7 | 1:176104861 | ACTCTCTACTGGCTG[G/T]AATTTCAAAATAATG | 64326 |
rs533294136 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176102746 | AAGATTCTGACCCTC[C/T]TTAAACTGTTCCTAA | 64326 |
rs533308983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176137437 | TCAAAAGAAAACTGC[C/T]TTCCAGAAACACTAT | 64326 |
rs533317217 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176197431 | TTGAAAAAAAGAAAG[A/G]AAACAGGCCTCAGAA | 64326 |
rs533317637 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176060890 | GAAGAAAAATATTTT[A/T]AAAAATGTGAGTTTT | 64326 |
rs533322213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176190183 | TCGGATCTGTCTGCA[C/T]TTTGAAATATTTGCA | 64326 |
rs533339452 | in-del | -/TATA | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176133082 | TGTACGTATATATAC[-/TATA]TATACACACATATAC | 64326 |
rs533339510 | in-del | -/ATA | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176037672 | CAATGACTATAATTC[-/ATA]ATATTAATAAAGAGA | 64326 |
rs533348592 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176064378 | ACTGCTCTAAGACAA[C/T]ATATGCTCAAAAATA | 64326 |
rs533353896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176151213 | GGATAAGGAAGCGTG[C/T]AAGAAAAAGAATAAA | 64326 |
rs533373179 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175965773 | TTTGTATTTGGAGAC[A/G]GGGTTTCATCATGTT | 64326 |
rs533374888 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175972994 | TGCGCCACCACACCC[A/G]GGTAATTTTGTATTT | 64326 |
rs533378619 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176103241 | TCATACCTGAATTTA[C/G]TGAAGTGACTTAGGG | 64326 |
rs533378877 | in-del | -/CGCCTGTAGTCCCAGCTACT | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176203208 | GGGCGGGGTGGCCGG[-/CGCCTGTAGTCCCAGCTACT]CGCCTGTAGTCCCAG | 64326 |
rs533408122 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176123162 | CCATCAGGGTTTAAA[A/C]AAACAATTATCTGAA | 64326 |
rs533421055 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176018284 | ATTAAACCACAATTG[G/T]CAGTAATTTAAAATA | 64326 |
rs533428444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175958795 | AGAAATAGAAAGCAA[A/G]AATCATCCTACAGGT | 64326 |
rs533438740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176006489 | CAGTGGCTGGTATGG[A/G]TTGTTCCTTTTCATG | 64326 |
rs533442254 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176115495 | GGCTCACGCCTGTAA[C/T]GCCAGCACTTGGAGA | 64326 |
rs533456281 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175955641 | CTTCAGCAAGATTGT[C/T]AGACACAAAGTCAAT | 64326 |
rs533486360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176158426 | GGAAAATAACAGATA[A/G]AAACCAATCTAGACA | 64326 |
rs533499383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176177866 | TCTCACATTTGTTAC[C/T]TTCAAGATAAGTAAA | 64326 |
rs533530236 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176091294 | AGAGAGCTGAGATCG[C/T]GCCACTGTGCCACTG | 64326 |
rs533532943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176132065 | ACAACCACTCTTACC[C/T]CTTCTATCAATAAAA | 64326 |
rs533540090 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176103815 | AATATAGGCAAAACC[C/T]AGAGTTAAAATCAGT | 64326 |
rs533542613 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175995429 | ATACAGACACAAAAA[A/C]CCCTTCAAAAAAATT | 64326 |
rs533545152 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176089205 | GGCTGGGGCAGGAGA[A/T]TCACTTGAACCAGGG | 64326 |
rs533547082 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176081664 | GTTAGTTTGAAGGAA[A/C/T]GTGTTTACTGGCACA | 64326 |
rs533550793 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175959306 | ACTGAAGGAAACTTC[A/T]TTGTAAGGGTATGTA | 64326 |
rs533563203 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175954327 | AGTAAAGCAGGAAGG[C/T]TGAACATTAATGATA | 64326 |
rs533597106 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176045928 | TCCAACAAAGACCTT[C/T]ATTTGATTAAGTGAA | 64326 |
rs533606408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176139385 | TTAGTTCAGCCACTG[C/T]GGAGACCGGAGTTGG | 64326 |
rs533615537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176147112 | AAGAAGCAATTTGCC[C/T]CCTGGTAAATCTGTA | 64326 |
rs533621708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176130343 | AAGTAAAAGAGACTA[C/T]GCTTGCCTACCAATC | 64326 |
rs533627107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176181956 | GTTTTGAGAGCAGGA[A/G]GTAAAGCTATTTAAG | 64326 |
rs533628639 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176038524 | CAACATGGTACAAGT[A/C]AAAGAAGAGATAGGG | 64326 |
rs533636391 | snp | C/G | 0.089084 | 0.191327 | intron-variant | RFWD2 | GRCh38.p7 | 1:176002976 | ACAGTCCCACCAACA[C/G]TGTAAAAGTGTTCCT | 64326 |
rs533637933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175966181 | AATCTATCAATAAAA[A/G]GTCTTGGTCTTTAAA | 64326 |
rs533638054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176007925 | AGCCTGGGTAATGGC[A/G]GGCGCCCCTCCCCCA | 64326 |
rs533642431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176140021 | AGCCAATATTACTTG[C/T]ATGATACATAATAAT | 64326 |
rs533648591 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176003595 | TTTCCCAGCACCATT[G/T]ATTAAATAGGGAATC | 64326 |
rs533680717 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176001778 | GGTATTTCTTATGGG[C/G]TAGGTCTCCTGACAA | 64326 |
rs533689169 | in-del | -/GAG | | | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207466 | TACAGTGAAAGAATT[-/GAG]GAGACTGGAATGAAT | 64326 |
rs533700252 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176159949 | GGAAGGAGTATTTCA[A/G]AGCCCCATATTATTT | 64326 |
rs533711954 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176088743 | GCTCGTACCTGTAAT[C/T]CCAGCATTTTGGGAG | 64326 |
rs533718974 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | RFWD2 | GRCh38.p7 | 1:176152668 | GGCCAGGCTGGTCTC[A/G]AACTCCTAAGTGATC | 64326 |
rs533725508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176029804 | ACCACTTCTATGAAA[C/T]GGGATTACGTAAGAA | 64326 |
rs533749373 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176162254 | ATAAATACTCCCTTT[A/T]TGTTTAACCTCAGGG | 64326 |
rs533761246 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176183834 | TGCTAAGTGAAATAA[A/G]CGAGTCACAAAAAGA | 64326 |
rs533761250 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176157533 | GAAAAACCAAGAAAT[A/G]TACATGCATCAGGCA | 64326 |
rs533785754 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176173871 | CGCACGTCTGTGATT[C/T]CAGCAACCAGAGAGA | 64326 |
rs533796437 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176022655 | TTAAAGGAATGTTTC[A/C]GTCAGTGAAAGGTAC | 64326 |
rs533798974 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175946208 | GATCAGTTAAAAAAC[C/G]TCGTTTTCATTTAAG | 64326 |
rs533807184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176029278 | TGCAAAATTTTGGTT[C/T]TGTATTTGAATAAGT | 64326 |
rs533826178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175993377 | TCCTCACCAGCAACG[A/G]AACAAAGCTGGATGG | 64326 |
rs533830628 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176174483 | GCCACTTAGAAGAAT[C/T]TGTCATTCTAGCAGA | 64326 |
rs533851677 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176186617 | TTTTAAGTTGAGTAA[A/C]ACGGTAATTCACTGG | 64326 |
rs533857316 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176125650 | TATAATGTAAAATCA[C/G]GTAATAACGATTCCT | 64326 |
rs533899837 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176205701 | AGACAATCAACACCA[A/C]CTTTCACTTCATATG | 64326 |
rs533911469 | snp | C/T | 5.51973e-05 | 0.00525315 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175968588 | TTAACCAGTCTTTTA[C/T]ATTCCAATTAACTAA | 64326 |
rs533924575 | in-del | -/CTATATTAAACTGTAAATTCC | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176136059 | ATTTCCTTAGGTAAA[-/CTATATTAAACTGTAAATTCC]CAGAATATTGGTAAT | 64326 |
rs533930344 | in-del | -/A | 0.267636 | 0.249377 | intron-variant | RFWD2 | GRCh38.p7 | 1:176045582 | AGCTTGTTTAGAAGG[-/A]AAAAAAAAAAAAAAA | 64326 |
rs533931084 | in-del | -/TT | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176012161 | GAATAGCCACTGTAC[-/TT]TTCAGCCTAAGCCAT | 64326 |
rs533940925 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207566 | GCAGGCGCGCGCCGG[A/G]CGCGGACGCTCACGG | 64326 |
rs533944695 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175975158 | TGCAAATCTCTGTAT[C/G]TAAAATACATAGGAT | 64326 |
rs533971429 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176110950 | TGAGATCAAGGGATC[A/G]AGACCATCCTGGCCA | 64326 |
rs533976289 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176022041 | ATTATCTTAGCATTT[G/T]CATTTTAATTAATGT | 64326 |
rs533980771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175946980 | TGACCATCTATTAAT[C/T]CATCCAGCATCCATA | 64326 |
rs533990903 | in-del | -/TAAC | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176057053 | TGAAAATCCTATAAT[-/TAAC]TGAGCATAGAAATGA | 64326 |
rs533998732 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176138558 | CTGAAACTCTTTCAA[A/G]TAACAGCTGCTCAAT | 64326 |
rs534007857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175952587 | CTTCAGGATGAAGGA[A/G]TATTATACTACATGA | 64326 |
rs534009273 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175949467 | CTCAGAAAACAGCAG[-/A]AAAGAGGCACTGTGT | 64326 |
rs534021992 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176201096 | CCAACATGACTATCA[C/G]AGGAAATGCTCACTG | 64326 |
rs534034802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992602 | AGATTATATCCCGCA[C/T]CTGGCTCGGAGGGTC | 64326 |
rs534124322 | in-del | -/A | 0.00755907 | 0.0610114 | intron-variant | RFWD2 | GRCh38.p7 | 1:176130135 | AGTATGTTTCAATAT[-/A]AAAAAAAAATCAGCA | 64326 |
rs534127136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176105763 | ACACATCAGTTGGTC[A/G]GCATTGTTTAGTAAT | 64326 |
rs534147561 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176116957 | TCTATATAGATTTAC[C/T]TGTTTATATTTCATT | 64326 |
rs534152558 | in-del | -/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176080252 | AAAGTATCACATCAG[-/T]TTTTTTTGTGATGTG | 64326 |
rs534155426 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176007602 | GTTGGAATACCCTGC[A/C]GTGTGAGATGTCAGT | 64326 |
rs534177191 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176069623 | CTTCTCCCTGACCAC[A/C]ATCCCCAGAGGGTTC | 64326 |
rs534185434 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176020898 | ATTTACAATGAGTTA[C/T]AAAATACTAAATAAG | 64326 |
rs534193865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176070451 | GTGGATCCCTGAGGT[C/T]AGGAGTTCGAGACCA | 64326 |
rs534196908 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176111313 | TTTTTGTGTGTGTGT[C/G]AGATGGAGTCTCGCT | 64326 |
rs534202619 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175988082 | ATTTGAGGTGTTCAG[C/G]GTTTCTACACAATAA | 64326 |
rs534205833 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176189084 | CTAACACGTACAATG[C/T]ACTTTAAACTGCTAA | 64326 |
rs534217583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176095928 | CACACAAATTAAATC[C/T]TGCATTAAATCCAGG | 64326 |
rs534232781 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176028017 | TGGGGGCAGGCAAGA[A/G]AGCGTGTGCAGGGGA | 64326 |
rs534244181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176020163 | TAAAAATACAAAAAT[C/T]AGCCAGGCATGGTGG | 64326 |
rs534246054 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176013526 | TAGTTTTTCTCCTTG[C/T]ATAATTTCTCATTTC | 64326 |
rs534261496 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176034834 | AAGTACCACAGCAAA[A/G]GCTCTGAGAAATGAA | 64326 |
rs534269741 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175981888 | GTATATGAAAAAATG[C/T]TCAATATCATTAATC | 64326 |
rs534274361 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175984522 | GCAGTACAGAAGGGA[A/T]ATGTGGGGTGGGAGC | 64326 |
rs534281813 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:175951174 | GAATCGCCTGAACCC[A/G]GGAGGTGGAGGCTAT | 64326 |
rs534286041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176202714 | TATATTAACAAGAAT[A/G]GTCAACAGGCTTCAT | 64326 |
rs534288033 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175954491 | TTCATTGAAAAAAAT[C/T]AATAAAATTGATACG | 64326 |
rs534314325 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176124393 | TTTTTATCCATTAAA[C/T]GTTCCCACCTCCCCT | 64326 |
rs534337903 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175977826 | TTTTATTCAATTTAG[A/G]AAATAATAATGTTTT | 64326 |
rs534339450 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176166598 | TACTGTATCAGATTT[G/T]TCATGGAGTTACTTG | 64326 |
rs534344286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176203395 | ATCTACATGCAAACG[C/T]ATACTTCTGCTGCAA | 64326 |
rs534356872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176108351 | ATTTCTGTAACTATT[C/T]TATTATGGCTGGGCA | 64326 |
rs534382496 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176055778 | TTTTTAAAAGCTCAT[G/T]AATTGATTTAGTAAT | 64326 |
rs534384794 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176026824 | TTCACCATTCAGAAG[A/C]CAAATTACAAGTATT | 64326 |
rs534395395 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175990313 | CAGAAAACTGTTTTG[C/T]ATGTCTTCAATCATT | 64326 |
rs534415588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176098302 | TACCATTATAATATG[C/T]AATTGAAACTATTGG | 64326 |
rs534433839 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | RFWD2 | GRCh38.p7 | 1:176049173 | AACAGAGCGAGACTC[C/T]GTCTCAAAAAAAAAA | 64326 |
rs534441340 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176056200 | TAATTTGAGATTTGG[C/T]ATATGATCTAGATTC | 64326 |
rs534468967 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176160150 | AATTCGAAGCCAAAA[A/C]GGAAACAAAGACTAA | 64326 |
rs534474884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176065331 | TTACAGTAATGTCCT[A/G]TCTTACTAAGAAGTT | 64326 |
rs534495585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176143401 | ATCACAGGTCTAGAC[C/T]GCTTCTCCAGTAAGA | 64326 |
rs534499559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176199295 | GCACTCCAGCTGGGG[C/T]GACAGTATGAGACTC | 64326 |
rs534501073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176063092 | GAGTCTCGCTCTGTC[A/G]CCCAGGCCGGACTGC | 64326 |
rs534517959 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176102779 | TCAGTGCTTGAGATA[C/T]TTTGCAGACCCTGCA | 64326 |
rs534527046 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175999733 | TTCCCACCACCACTG[G/T]ACAAGGGTTCCCTTT | 64326 |
rs534551389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176186954 | CACACAGCTCCATCA[C/T]CCGTTAGTTTATTTA | 64326 |
rs534552091 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176113689 | TGCTAGCAGCAATAA[A/T]TATGAATAAGTGAGA | 64326 |
rs534557152 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176139058 | AATATCCAGAATCTA[A/C]AAGGAACGTAAATAA | 64326 |
rs534558079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175973978 | TAAAATGTGCTTATG[C/T]AAGTGGTAAGAGATT | 64326 |
rs534570959 | snp | G/T | | | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176208314 | AAGTACAAAAAATTA[G/T]CTGGGCATGGTGGCA | 64326 |
rs534575844 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176009238 | CTGCATCTGATTATT[G/T]TCAACAATACTGTGG | 64326 |
rs534582722 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176074350 | AAGAAAAGCAAAAAA[C/T]CAACAGAGCTGTGAG | 64326 |
rs534583100 | snp | G/T | 0.0228947 | 0.104514 | intron-variant | RFWD2 | GRCh38.p7 | 1:176024131 | AGATGTGGTGGCTGG[G/T]GCCCGTAGTCCCAGC | 64326 |
rs534595073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176073925 | TTCAACATTATCTGC[C/T]TTCTCAAATACTTGT | 64326 |
rs534599030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176164474 | GCAATCTAGTCATTC[A/G]TGCCCTTGCCAGTGG | 64326 |
rs534611054 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176063107 | GCCCAGGCCGGACTG[C/T]GGACTGCAGTGGCGC | 64326 |
rs534688207 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175948884 | AATAGTAACATGGGG[A/G]CTGGGCGCAGTGGCT | 64326 |
rs534695099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175994453 | ACACAGACTGGCAAA[C/T]TGGATAAAGAGTCAA | 64326 |
rs534719555 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175963033 | GAATGTTACATGTGG[G/T]TGTTTTCTGTTATTC | 64326 |
rs534727567 | snp | A/T | 0.0349115 | 0.127424 | intron-variant | RFWD2 | GRCh38.p7 | 1:176051581 | ATCTTCTACTTATTT[A/T]AAAAAAAAACAAACA | 64326 |
rs534735217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176163969 | ATTCTTCGGTTTAGA[C/T]AGATTCTATTTTACC | 64326 |
rs534741001 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176035249 | CTCAGAGAATATATA[C/G]AAACTATTTTTTTTT | 64326 |
rs534743371 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176170595 | CAGTAAATCACGCTG[A/C]AAAGAGATATGCTGT | 64326 |
rs534755217 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176179372 | TGGGTTTTAGCAAAT[A/G]ACTTTTCTTTAAAAT | 64326 |
rs534764721 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176015356 | ACCAAATGCAGGTCC[A/G]AATCGTTGCAGTTTG | 64326 |
rs534766754 | in-del | -/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175986693 | ACAGACAATATGATA[-/T]ATGGTTATAACTGAG | 64326 |
rs534768981 | snp | C/T | 8.26276e-05 | 0.00642705 | missense, intron-variant, utr-variant-5-prime | RFWD2 | GRCh38.p7 | 1:176162936 | TTGGCCAAATCAAGG[C/T]TATCTTGGTCAGTTC | 64326 |
rs534785151 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176150806 | GTCCCCAAAATGTCA[A/C]TGTAAAAGGAAAGTG | 64326 |
rs534786285 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175992167 | AATGCATAATAATCA[A/C]ATCATGGAGAATGGC | 64326 |
rs534806742 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175972161 | AAGGTGGTTCTTGGT[A/C]CTCACCTTCAGAAAG | 64326 |
rs534812167 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176112893 | CTGCAAATGACAGGA[C/T]TTCATTCTTTTTTAC | 64326 |
rs534819838 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175973476 | TTGAATTTTACTGCA[G/T]GCAGAGCTACAAGTT | 64326 |
rs534829093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176155512 | TAATATGAAACATTA[C/T]AACAACATATGACTA | 64326 |
rs534845209 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176053776 | TCACTCTGTTATGTA[A/T]TTACTTTCTTCTTTC | 64326 |
rs534874645 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | RFWD2 | GRCh38.p7 | 1:175994125 | ATTTTCAACCCAGAA[C/T]TTCATATCCAGCCAA | 64326 |
rs534889969 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176157008 | TTCGAGACCAGCCTG[G/T]TCAACATGGTGAGAC | 64326 |
rs534892143 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176176094 | GACTATTAGTCTTCT[A/G]TTCCTCATTTTCAAC | 64326 |
rs534928060 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176150110 | ACAAGTGCCCAGATG[A/T]TAAGAATAAGCCAAT | 64326 |
rs534928803 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176091055 | TGCTTTTCAAGAGCA[A/G]TAGAAAGAAGCTAGA | 64326 |
rs534938572 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176008996 | AGCCTTCACTTCCTG[C/T]TTACACAGAGCTCAT | 64326 |
rs534981635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176107468 | GGATACAGAAGTCAG[C/T]ATGAAGGAGCTCCAA | 64326 |
rs535019901 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175963598 | GATTTTAAATTAAGA[C/T]AGCACTTAGTATACT | 64326 |
rs535024200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176182137 | CTTTTTTAAAAAATG[C/T]CACAATGGATATGTA | 64326 |
rs535032200 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176203363 | AAAAAAGTCAACCTT[A/C]TCATAAAGAGCTTAC | 64326 |
rs535038653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176047569 | GTGTATGAATGTATC[C/T]TCAATATCTATGTAT | 64326 |
rs535039076 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176043940 | TATCAGTTCACAATC[A/G]TTATTCTGCCCACAA | 64326 |
rs535049242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176008647 | TATACCTTTTTTTAC[C/T]GAAAAGCAGACACTT | 64326 |
rs535053551 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176004508 | ATAGATAGTTCTTAT[A/T]ATTTTGAAATACGTC | 64326 |
rs535055347 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175977868 | CACTTCAGCATATTA[C/T]ACCAATTCAAATAGT | 64326 |
rs535078026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176096995 | CTGTGCAACCTTTGC[C/T]ATTTGTTGATTCTCT | 64326 |
rs535090753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176097953 | TTAAAAGGAAAATAA[A/G]AGCTGTAGTGCCTTT | 64326 |
rs535094894 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175973833 | ATCATATGTAACAAA[C/G]AGAAGTGCAGGAAAG | 64326 |
rs535098819 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176048542 | AACTATTCATCTATC[C/G]CAACTCAATTTATAC | 64326 |
rs535105638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175983232 | TTTGGGTGTGTCCCC[A/G]TCCAAATCTCAACTT | 64326 |
rs535107475 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:175966985 | TTCTTCATCACAAAG[A/G]AACACTTTCAAAATC | 64326 |
rs535138997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176016149 | ATAGAAATGTCTGGA[A/G]TTTTTTTTAGCTAAG | 64326 |
rs535139567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176007063 | CTTTTTATTCTTTTT[C/T]CTCTAAACTTCCCAT | 64326 |
rs535142315 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176008197 | ATGCCTCGCCCTGCA[G/T]CAGCTCGCGCACGGT | 64326 |
rs535152733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176151838 | TTTTTAAATATTTCA[C/T]TATAAATGAGTAATT | 64326 |
rs535183888 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176054650 | ATTTATACTTGTGCG[G/T]TAAGTCCCATCCTTG | 64326 |
rs535187449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176152534 | CTCACTGCAGCCTCC[A/G]CTCCCCAAGGTGAAG | 64326 |
rs535188668 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176191302 | TAAAAATATGCATCA[C/T]TGTGATTATGAAAAT | 64326 |
rs535195502 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176075769 | CAGTAGTTTGGGAGG[C/T]CGAGGCAGGTGGATC | 64326 |
rs535216268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176044674 | TCAAATTCCAGATCT[A/G]TTACTTATTAGCTGT | 64326 |
rs535219339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176134446 | ACTACTAAATGAAAC[C/T]AGGCTTTATTCTAAA | 64326 |
rs535223336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176126430 | TTTATCATGAAGGAA[C/T]ATTGAACTTCATCAA | 64326 |
rs535228360 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:175946639 | ATCAATTTTCTTTCC[-/T]TTTTTTTATGGCTAG | 64326 |
rs535238712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176030672 | ACTGTCTGAGCTACA[A/G]GGGTAACTAAGATTA | 64326 |
rs535284736 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176041668 | CCTGCTTGGATTTTT[A/T]AAAAAATAAACAGTA | 64326 |
rs535285912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176076142 | ACATTGACACAGAGT[A/G]CTACACCCAACAACC | 64326 |
rs535295797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176035431 | GTCTAATACACTAAC[A/G]TAATTAAAATCCCAG | 64326 |
rs535306228 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176188547 | TGCTGAGCGAGTCTG[C/T]TGGCAGCTCATTTTT | 64326 |
rs535315850 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176137933 | GAGTTCAGTCTAGGG[A/G]AGATGGCAAATAAGA | 64326 |
rs535327157 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176142191 | ACAAATACATGATGT[A/C]ACAGAGAGAGCAACC | 64326 |
rs535331842 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176004886 | TGAGTTAGGGAGGAT[A/T]CCCTCTTTTTCTATT | 64326 |
rs535334334 | in-del | -/AAAC | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176098471 | AGACTCCATCTCAAA[-/AAAC]AAACAAACAAAAAAA | 64326 |
rs535345816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175972829 | AATAACTGCACATAA[A/G]CCTTATTTATTTAAT | 64326 |
rs535362318 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176113320 | GTATTTTTACATATA[A/C]CTATTGACCACTTGT | 64326 |
rs535363165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176185739 | GGATGAAATCCTTGA[A/G]CAGCTGCATCAGCTT | 64326 |
rs535364181 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176085316 | TATTCTCATGATACT[-/C]CTGTAAACTTATTTA | 64326 |
rs535365162 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176094423 | TATGCAGAGATAAAT[G/T]TTTTGAAAATACATA | 64326 |
rs535380545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176191879 | CTCTATGAATAAGGA[A/G]ACGAGAGGTAAGGAA | 64326 |
rs535390721 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175960118 | TATATTCATGGAAAT[G/T]CCAGTAACTGGTTTT | 64326 |
rs535403457 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176189761 | AACATAATACTGTCC[C/T]TAGAAACAATGAAAG | 64326 |
rs535408188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176139115 | ATTAAAAAATGGGCA[C/T]AGACATAAACAGACA | 64326 |
rs535416299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176090427 | TTTGTCTCCAAATAA[A/G]CTTCTTTAAATATTT | 64326 |
rs535421107 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175966587 | GTATCATATTGACCC[A/C]GTAAGCTTATCACAT | 64326 |
rs535432214 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176145556 | TGGATACACATATAA[A/C]ATAGTAGTATTTTTT | 64326 |
rs535447628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176129150 | TACAAATTCACAAGG[C/T]ATTAGATCACTATCC | 64326 |
rs535452061 | in-del | -/AAAG | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176027483 | ACATTTAAACCTACA[-/AAAG]AGTTATTTGTTTTAA | 64326 |
rs535465647 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176032714 | AAAATGATGAAGATA[C/G]AGGCTACAGAGTCTT | 64326 |
rs535481362 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175949957 | AAATTGTAGTATATT[A/C]TCTTACAGTATGAAA | 64326 |
rs535481597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176171418 | TTCTGGATAAGACTT[C/T]GGCTTAAGGGAATGT | 64326 |
rs535483860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176129854 | CTGCAATGGCTTTGA[C/T]GAGAATTTAAAATCT | 64326 |
rs535494946 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176011551 | CAGAGAGTATGCTTA[A/T]CATACCATCTTAACA | 64326 |
rs535496093 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176087957 | CATGTCCTTTGTAGC[A/G]ACATGGATGAAGCTG | 64326 |
rs535550699 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176006256 | TCTCTGCACGTGAGA[C/T]GGGTTTCCTGAATAC | 64326 |
rs535563795 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:175973387 | CATCTTTCCATTCTC[A/G]TATTTTTAAACCAGC | 64326 |
rs535576853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176087644 | AAACAGGAACGCTTT[C/T]ACACTGTTGGTGGGA | 64326 |
rs535581195 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175994877 | CAGGAATTGAACTCA[C/G]CTCTGCACCAAGCAG | 64326 |
rs535594002 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176034659 | TGGAGAAGGAGATTC[C/T]ACAGTTCTGTGCATT | 64326 |
rs535604506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176124418 | TCCCCTGCCCCCCAG[C/T]CCCGTACTACCCCTT | 64326 |
rs535604641 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176131495 | TTCAGTGACCTGACA[A/T]ATAATAAAGATATTC | 64326 |
rs535610709 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:175997334 | ATTCAGGACATAGGC[A/G]TGGGCAAGGACTTCA | 64326 |
rs535615708 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176170989 | AATTAGCCGGGCTTG[G/T]TGGTGGGCGCCTGTA | 64326 |
rs535636415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176026177 | TAGGTTCCTATTTTC[C/T]AAGAAGGAGAAAATT | 64326 |
rs535642365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176159006 | ATGTGGTAGTAATTG[C/T]ATTAAAAACTCTAAA | 64326 |
rs535657309 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176018908 | AGGTGGTTCACGCCT[A/G]TAATCCCAGCACTTT | 64326 |
rs535677555 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175944842 | CAACTGTGGCTCAAT[A/G]AACTTTTATTGTTTT | 64326 |
rs535683141 | snp | A/T | 0.0267878 | 0.112589 | intron-variant | RFWD2 | GRCh38.p7 | 1:176000468 | CACTAGTATCACTGT[A/T]AACATGTGAGTAATG | 64326 |
rs535719361 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176025592 | TATTATGAAATCTCA[C/T]TGAAAGACAGAAAAC | 64326 |
rs535736717 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176089773 | GGTTTTACTTAACCC[C/T]ATATAATCTCTCTTA | 64326 |
rs535745247 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176002355 | TTTAGTTTTTATTTA[A/T]TTATTTATTTTTATT | 64326 |
rs535745769 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176033289 | TGTCGGGGCGAGGGT[G/T]GGGGGAACATGCCTG | 64326 |
rs535771139 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176041141 | ATTAAATACAATGCA[A/G]CACATAGAGATTTCT | 64326 |
rs535772317 | snp | C/T | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176144672 | TTTAATACAAGGTGG[C/T]ATTGCGAAAAAGACC | 64326 |
rs535774943 | in-del | -/TATT | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175976194 | TGGGAAAGGTATAAC[-/TATT]TTATTCTGTTCAGAA | 64326 |
rs535808312 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175995116 | CCGCTCAACTACATG[C/G]AAAGTGAACAACTTG | 64326 |
rs535814041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992329 | AGCGACGCAGAAGAC[A/G]GGTGATTTTGCATTT | 64326 |
rs535816286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176067863 | ACGTTTACCCCCAGA[C/T]ACTGCTGTGGGGTCA | 64326 |
rs535822785 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176030971 | GGCACAGTGAGAAGA[A/G]GGCCATGTGTGAAGA | 64326 |
rs535837489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176039742 | AGAAGAGCAGAGAAA[A/G]ACTAAAGATAAACTC | 64326 |
rs535854435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175950627 | AATAAAATAAAAGTG[C/T]GAGTCAGTAATTCTT | 64326 |
rs535874050 | snp | C/T | 1.64868e-05 | 0.00287109 | intron-variant | RFWD2 | GRCh38.p7 | 1:176081145 | TAGTAATTTGACCAA[C/T]ACTTACCTAGAGACT | 64326 |
rs535884233 | in-del | -/TA | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176059292 | ACCTAAGAAAAAAAT[-/TA]TCTTTGTATGGCAAT | 64326 |
rs535889456 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176126254 | GGACTTTTAGTACTA[C/T]GTTGAGTAACATTGG | 64326 |
rs535906659 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176144126 | GAGTAAGACAAGAAA[A/C]ATAAATAAAAGATAT | 64326 |
rs535916815 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176044465 | TTATGGAAGAAGTTA[C/T]TTAGAAGGCAGTTAA | 64326 |
rs535946448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176135918 | TTAAACATGTTCTAT[A/G]TATCAGCAAAAAAAA | 64326 |
rs535975809 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176046601 | CATTCAGTTCTAATA[A/C]CCATATTACAGCTTA | 64326 |
rs535987648 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176133162 | TACGTACATATATAT[A/G]CGTATGTACACACAT | 64326 |
rs535988957 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175965828 | ACCTCGTGACCCACC[C/T]GCCTCAGCCTCCTAA | 64326 |
rs535990748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175958329 | TCCCAACATAATATA[C/T]AAACCCCTTATCACT | 64326 |
rs535991093 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176177450 | AATCCCACTTCTCTT[A/T]AAAAATCATATATGT | 64326 |
rs536017205 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176023445 | GTAAACAGGCCAGGC[A/G]TGGTGGCTCACGCCT | 64326 |
rs536022126 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176030970 | AGGCACAGTGAGAAG[A/G]AGGCCATGTGTGAAG | 64326 |
rs536022938 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176204860 | TTGAACCCGGGAGGC[A/C/G]GGGGTGGCAGTGAGC | 64326 |
rs536030189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176113220 | ACATTTGTTACTTCT[A/G]TCTTCTTGATAATAC | 64326 |
rs536048162 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176007822 | GCCCTGTCCCCAGAG[G/T]TGGAGCCTACAGAGG | 64326 |
rs536063693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176107533 | TAGTAACAGAATATA[C/T]ATATTAATGACCCAG | 64326 |
rs536070760 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176152035 | AATTGTTGGCTGCAA[A/C]ATCCTAGCACTGCGG | 64326 |
rs536084269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176197731 | TAAAAGATGTAAAAG[C/T]ATATTCATATACAGA | 64326 |
rs536087160 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176109890 | AGCCTCTTGGATAAA[C/T]AATAAGTTCATTTAT | 64326 |
rs536095003 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176019314 | CTAAAAATACAAAAA[A/T]TAGCTGAGCATGGTG | 64326 |
rs536109335 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176171894 | TGAAATTTCTGGTAT[G/T]GAATAAAAAGCTTAC | 64326 |
rs536117328 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176081720 | AAATCCCGTTTATAA[A/T]AACATTTTAGATAAA | 64326 |
rs536122958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176169338 | TTTATTTGTTTGATC[A/G]ATTGTATACTACTAC | 64326 |
rs536134887 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175989554 | TTTAACTGGTTTTTG[G/T]TTTTTTCATTAAAAG | 64326 |
rs536167684 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176208030 | CAGACCCAGCTCAGT[C/G]GGAACCTAGGTTTAT | 64326 |
rs536171054 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175993671 | GAAATGAATGAAATG[-/A]AGCGAGAAGGGAAGT | 64326 |
rs536173568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176165843 | TGAACTGCAGATACC[C/T]TACACAAGAAAAGTG | 64326 |
rs536183452 | snp | G/T | 0.000167608 | 0.00915292 | intron-variant | RFWD2 | GRCh38.p7 | 1:176163024 | AACACAACAACTTCC[G/T]ATGAAGACTGTTTTA | 64326 |
rs536199445 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176075486 | TTATTCGTTCTAAGA[C/G]ATTTGAACACAAAGT | 64326 |
rs536207074 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176118682 | GATCACTTAATCTCA[A/C]ATGGTCAAGGCTGCA | 64326 |
rs536208311 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176199456 | CTAAAAATGTGAAGA[C/T]GTGTCTGCACAAAAA | 64326 |
rs536216287 | snp | A/C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175966990 | CATCACAAAGGAACA[A/C/G]TTTCAAAATCAGTTA | 64326 |
rs536241825 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176161244 | AATTTACTGTCATTT[A/T]CATCATTTCAAAAGG | 64326 |
rs536242750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175946367 | GCTAGGATTTGCTGC[C/T]TTGGCTGATGGATTA | 64326 |
rs536242907 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176109970 | ACAATTCTGACCACA[C/T]TCCAGAAATTTTTGA | 64326 |
rs536260091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176175244 | CTGCCGCAAAAGCAG[A/G]AACAGTAGGGATGTA | 64326 |
rs536274284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176078197 | GCCAAAGCAGTCCTA[A/G]GCAAAATGAACATAC | 64326 |
rs536288928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175947083 | TGTAAGGAGACACAG[A/G]CCCATGATTTGGGAT | 64326 |
rs536291178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176105436 | AGGCTAAAGACAAAC[A/G]GAATTTCAAAGAAAT | 64326 |
rs536309704 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176076788 | AATGACAAAGATGAC[A/G]TTACAACCAATACCA | 64326 |
rs536317423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175954391 | GCAAGTTACACATGA[C/T]GTAAGTACAAGAATG | 64326 |
rs536323250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175945487 | ATATGTTGGAATCTT[C/T]CCACATTCTTATGAA | 64326 |
rs536323873 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175987573 | ACATAATTTATTTCC[A/G]TTTCTCAGTATAGGA | 64326 |
rs536326923 | snp | A/T | 0.0193772 | 0.0965046 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992900 | AGCAGTGGTTCTCCC[A/T]GCATGCAGCTGGAGA | 64326 |
rs536345017 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176123451 | ATCAAAGTATATCTA[C/T]AATAATTAAAGGGGA | 64326 |
rs536346694 | snp | A/G | 4.05277e-05 | 0.00450135 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176206688 | GCTGCCTCCTACGCC[A/G]GCGCTGGGCCTGGCC | 64326 |
rs536375979 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176036502 | TAATGAAAAAAACAA[A/C]AAAACAAAAAAAAAA | 64326 |
rs536387685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175988103 | TACACAATAAAAAAG[A/G]GAAGGACTAATGCTC | 64326 |
rs536395911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176174630 | CTTTTAGAGCAGATA[A/G]AAAGGAAAACCATAG | 64326 |
rs536402509 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:175976186 | TTGTTAATTGGGAAA[A/G]GTATAACTATTTTAT | 64326 |
rs536404081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175983702 | AACTCCCTAGAGACT[C/T]GTTCAATGGCTTTGA | 64326 |
rs536417736 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176099074 | TGTTAAGTTATTGTA[A/T]ACCACAGAGATAATC | 64326 |
rs536424918 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176202088 | ACTTTAAAAAAAATT[G/T]TACCAGTGTACCCAG | 64326 |
rs536432485 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175968730 | AGGCTGTGAAGAACA[A/T]ACACAAGGGAAGAAG | 64326 |
rs536445482 | in-del | -/T | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176001097 | TTAGAAAAAAGGAAG[-/T]TGCAGCTCACTACCA | 64326 |
rs536446583 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176101044 | CATAGATAAAGGTCA[C/T]GCTACTATCCATGGC | 64326 |
rs536448929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175962123 | GATAGGAGCAGTTTT[C/T]CTTTGGTGTTGTAGA | 64326 |
rs536460574 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176187128 | AGAATCAAAGAAGGT[C/G]TCCATTCTTTTTTTG | 64326 |
rs536464045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175977116 | CTGAATCTTGAAGTC[A/G]GATTTACTTTCTACA | 64326 |
rs536469542 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176104590 | TAAAGAAACACAAAA[C/T]TATTCTGAGATATAT | 64326 |
rs536480901 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176140970 | GTAAAGAGTAAGTAA[C/G]TCTCAGAATCCCTTA | 64326 |
rs536486004 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | RFWD2 | GRCh38.p7 | 1:176003656 | GTCAGAGATCAGATA[C/G]TTGTAGATACGTGGC | 64326 |
rs536486537 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176195137 | GGGAGAGGAGAGAAA[A/G]AGGGAGAGGGAGAAG | 64326 |
rs536488403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176202570 | ACAGGTGGTGGCACC[C/T]GTCTCTAATCCCCGC | 64326 |
rs536508861 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176078870 | GAAGACATACAAGTC[A/G]CCAACAAGCATATGA | 64326 |
rs536514052 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176162350 | AATTTCACATTTTAC[A/G]TCTTTAACAGTTACG | 64326 |
rs536515529 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176063779 | TAAAAATACACAAAT[A/G]GGAAACTTTCTGCTA | 64326 |
rs536527177 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176203065 | CTTCTCGGCCGGGCG[C/T]GGTGGCTCACGCCTG | 64326 |
rs536528605 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | RFWD2 | GRCh38.p7 | 1:175965626 | TGGAGTCTCGCTCTG[C/T]CGCTCAGGCTGGACT | 64326 |
rs536553871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176056815 | TTGTTTTCTGTGTTA[C/T]TCTCCTAAATGGGAA | 64326 |
rs536554007 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176103373 | CTGGAGATTAAGCTC[C/T]ATAAAACTCTATAAA | 64326 |
rs536556843 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176075592 | TTTTAAGAGATGCAG[A/G]TAAGTTTCTGAGATT | 64326 |
rs536566371 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176007951 | CCCCAGCCTCGCTGC[C/T]GCCTTGCAGTTTGAT | 64326 |
rs536588324 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175990020 | TCTACTCTAACCTTT[A/C]TTATTTCCTTCCTTC | 64326 |
rs536589783 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176199433 | ATTCACTACTAGATA[G/T]TTTTACCCTAAAAAT | 64326 |
rs536598598 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176064946 | TTTTTCAAGCTTGTA[C/G]TAGCTACCACTTCTT | 64326 |
rs536599491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176072516 | TCATTTCTCAACCAA[C/T]CCCAGATGGTCAATA | 64326 |
rs536611611 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176178767 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCCGGGAG | 64326 |
rs536612969 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176108757 | CTGAATGTGTGAATT[G/T]TTGTCTTTTAAAAAT | 64326 |
rs536619196 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176193538 | CCATCAACTGAAATA[A/T]AAATTATATTAAAAT | 64326 |
rs536633043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176021186 | AATATGTGCTAATTA[C/T]TAGGCATATTTATGG | 64326 |
rs536633506 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176063204 | AGCTGGGACTACAGG[C/T]GCCCGCCACCGCGCC | 64326 |
rs536636421 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176067660 | ATACAAAAGCTTGCA[C/T]TCATTCTCCAAGCCC | 64326 |
rs536653624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176102174 | GCCTGGTCTCTCTTG[C/T]CCCTGGGTGGTGACC | 64326 |
rs536665000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175972263 | AAGCAGGTGATCAAC[A/G]GACCATACTTTGAAA | 64326 |
rs536668091 | snp | A/G | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176176698 | ATAGCATATGCAGCT[A/G]CTGGGAGGGTGAGGC | 64326 |
rs536685925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176197016 | AAATTGTATTTCCAT[C/T]CCTCGCAAAAGAAAA | 64326 |
rs536714690 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176028193 | TGGGTGGGGACACAG[A/C]CAAACCATATCACTG | 64326 |
rs536748274 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175957421 | AGTGTAGTAACATGC[C/T]GTACAAATTTGTAGC | 64326 |
rs536748471 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175956148 | AGTATTATTAGGATA[A/G]ACATATAAATCAAAG | 64326 |
rs536749987 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176195982 | CACGCAATATACCCA[C/T]GTAACAAACCTGTGC | 64326 |
rs536758338 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176203457 | TCATTTGAGATAGCT[A/G]GAAAAGCTAATACAA | 64326 |
rs536779673 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176086952 | GCCTCAGAAATAACA[-/C]CACACAGCTACAACC | 64326 |
rs536781237 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176160300 | CTTTAAGTTCTGGGA[C/T]ACGAGTGCAGAATGT | 64326 |
rs536822268 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176065977 | CTCAAACACCTGCCT[C/T]GGCCTCCCAAAGTTC | 64326 |
rs536835177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176050013 | CATTTCTGCCATCCA[C/T]TGTCAGCAGTAATAA | 64326 |
rs536847101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176136108 | ATGTATTCTTATATT[C/T]CTCTTTTAATTAACC | 64326 |
rs536853448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176140374 | TGATATAACCTATCC[A/G]TAAGAAAGTCTGACA | 64326 |
rs536859008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175966376 | TAGGTCAGTGACTTA[A/G]TTAAGAATTTTATAT | 64326 |
rs536859873 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176091492 | AATATTACTATTAAT[C/G/T]GTCATATCTAGTTTA | 64326 |
rs536871265 | in-del | -/G | 0.00755907 | 0.0610114 | intron-variant | RFWD2 | GRCh38.p7 | 1:176075245 | GAAAAATAAAGGAAT[-/G]TATGATTTTTGTCTT | 64326 |
rs536872091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176001486 | CTTTTGTTTCCAAAG[C/T]TGATATACTACAGTG | 64326 |
rs536896472 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176008115 | CGATTTTCCAGGTGC[A/G]TCCGTCACCCCTTTC | 64326 |
rs536901542 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:176005921 | TTGACTTTCTGTCTC[A/G]TTGATCTGTCTAATG | 64326 |
rs536912617 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176007618 | GTGTGAGATGTCAGT[G/T]TGCCCCTGCTGGGGG | 64326 |
rs536921705 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176056011 | TTTTAGCTATGTCCC[A/G]TAAGTTCTGATACAC | 64326 |
rs536954891 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176147222 | AAACACGCAAATAGA[A/C]TTACATGGAAGAAGA | 64326 |
rs536963860 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176037445 | AAAAAACACATAGCA[C/T]ATAGAAGAGGAAAAT | 64326 |
rs536973748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175965521 | CTTTTAAAATTCAAA[C/T]TTCTTTTGTTTTTGG | 64326 |
rs536978692 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175968146 | AAGTGCTGGGATTAC[A/G]GGTGTGAGCCACCAT | 64326 |
rs536980035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176096373 | TCAGGATGGTTGGGC[A/G]AATGGCAGCTCCCCA | 64326 |
rs536998124 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176188718 | GAGCCACAAATTGCA[A/C]CCATATTAGATGGCA | 64326 |
rs537000897 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176044010 | AAAAATAAAAATTAA[C/G]AAGTAATGACCCTAA | 64326 |
rs537020459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176017820 | GTGAGCCACTGTGCC[C/T]AGACTCATTATTAAT | 64326 |
rs537025021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176204048 | GCTGCTTCTCCTCCA[A/G]TCTGTGCCGTTTAAG | 64326 |
rs537026511 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176150272 | AATTTACAAGTCAAG[A/G]CAAATAAGGAGAGAG | 64326 |
rs537030568 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176022298 | GCCTCACTTCCCTGG[C/T]AGGATCCACAGTGCC | 64326 |
rs537043883 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175963658 | TTTATGGTCTTTTGT[A/C]CAGGTACCTTCCTTT | 64326 |
rs537050747 | snp | C/T | | | intron-variant, downstream-variant-500B, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175967940 | TGGCACAATCGCAGC[C/T]CACTGCAACCTTCGC | 64326 |
rs537057821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176109167 | ATTTTGAAGCAATTA[A/G]GCCATTTACTTGCCC | 64326 |
rs537066925 | in-del | -/A | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176177278 | GTGTGCCTCCCTATT[-/A]AAAAAAACACTCCTT | 64326 |
rs537076439 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175983391 | CCCTGTACAAGTTTT[A/C]TTCTCTTTTCTGCTG | 64326 |
rs537087060 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175964854 | CACAAAAAAACTCAC[A/G]ATCTATACTATATCT | 64326 |
rs537103146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176008663 | GAAAAGCAGACACTT[C/T]GGAAAATACTATGTG | 64326 |
rs537110167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176024817 | AAAAAATAAAATTTA[A/G]AAGCAATTCCATTCA | 64326 |
rs537118577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176148449 | ATCCAGAGCACAGGA[C/T]TTTGACTATTTAATT | 64326 |
rs537121477 | in-del | -/TCTC | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176099538 | CTCTCTCTCTCTCTC[-/TCTC]CCTGGCTTCTCCAGA | 64326 |
rs537123175 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176057903 | AGGAGCGTCTCTGCC[C/T]GGCCGCCCATCCTCT | 64326 |
rs537139434 | in-del | -/ACAG | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176148301 | AGAACATAGCACATA[-/ACAG]ACAATTTACACATTT | 64326 |
rs537154629 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176088861 | TTAGCCAGGCATCGT[A/G]GTGCATGCCTGTAAT | 64326 |
rs537157735 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176051590 | TTATTTTAAAAAAAA[A/C]CAAACAAACTGTAAA | 64326 |
rs537162385 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176004906 | CTTTTTCTATTGATT[C/G]GAATAGTTTCAGAAG | 64326 |
rs537173246 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176152348 | CCTTCTGGAAAATTG[A/G]TATCAGGGACTGGGA | 64326 |
rs537174310 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175989243 | AAAAATCTACTATTT[A/C]AGAAAAAGTACATAT | 64326 |
rs537180393 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175970293 | TGGGCTAAAAAATGA[C/T]GAGAACTTAGTTAAG | 64326 |
rs537191071 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175985081 | TGATCAGTTTTGAAA[A/T]GTGAGGACATGAAAT | 64326 |
rs537194134 | in-del | -/AT | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176155392 | AAGAGCAAAGCAGAC[-/AT]AGCAGAGGAAAGGAA | 64326 |
rs537212985 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175991000 | TAATAGGTTGCACAT[C/G]TGAAATCAAAAAATC | 64326 |
rs537216740 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176122798 | AAAGTTTTTTTTGTA[A/C]GAGGAGTTTCCTTAG | 64326 |
rs537238499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176144833 | ATCCATATGAAAATA[C/T]CTCTATACCTCACAT | 64326 |
rs537241669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176031355 | GAGAAGAAACTAAGC[C/T]AAATATAAATGAGGC | 64326 |
rs537245195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175965862 | GTTGGGATTACAAGC[A/G]TGAGCCACCGCACCC | 64326 |
rs537255423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175958997 | AATCAAAACCTGACA[C/T]GGACAATGCAAAAAA | 64326 |
rs537275397 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175973013 | AATTTTGTATTTTCA[A/G]TAGAGATGGGGTTTC | 64326 |
rs537285076 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176136804 | TGATTTTACAATAAA[A/T]GTATGAGATGAATGA | 64326 |
rs537286486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175949742 | AAATAATGACAGGAC[A/G]ATGAAAAATTTAAAG | 64326 |
rs537324518 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176060344 | CCTTTAAAATCAATA[C/T]ACTTAATATCAACTT | 64326 |
rs537328252 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176195961 | GGGTGACAAGATCAC[C/T]AGCATCACGCAATAT | 64326 |
rs537361616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176053916 | CCTAGTTAAATTTCT[C/T]TACTCACTCTACATT | 64326 |
rs537365261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176006303 | TTGACTCTTTATCCA[A/G]TTTGCCAGTCTGTGT | 64326 |
rs537367533 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176068532 | TATTTACAACATGCC[A/G]TATAAAACACAGAAA | 64326 |
rs537374085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176038368 | CAAAATCTCAGCAGG[A/G]TTTTATGTAGGTACT | 64326 |
rs537450210 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176132303 | TGTGTCAACTTAAAT[A/G]TCACCTCCTTGGAGA | 64326 |
rs537462387 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176041718 | CACCGGTAATTCCAG[C/T]ACTTTGGGAAGTCGA | 64326 |
rs537471085 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | RFWD2 | GRCh38.p7 | 1:176002835 | TGTGCATGTGTCTTT[A/C]TAGCAGCATGATTTA | 64326 |
rs537489951 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176005166 | TAGTATTCTCTGATG[A/G]TAGTTTGTATTTCTG | 64326 |
rs537490577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176099768 | TGGCCTCATACCCTT[A/G]TCTACACAGCTGCTG | 64326 |
rs537492640 | in-del | -/TAAA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175951461 | ATATATATATATATA[-/TAAA]AACTTCCATTTTTGG | 64326 |
rs537498663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176013333 | ACTTAGCTAGGGGGA[A/G]AAACACAAGATGATG | 64326 |
rs537524831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176156213 | GCCTGCAAACATATT[A/G]TCCTTGAAGTAGCAT | 64326 |
rs537533218 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | RFWD2 | GRCh38.p7 | 1:176108048 | ATTTTTTTTTTTTTC[C/T]ATAAAGGACATTAGT | 64326 |
rs537535578 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176100860 | GGAGTCCGTGCAACA[A/C]CCCCACCCCCCAAGA | 64326 |
rs537543018 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176185151 | TCGACAATGCTTGTA[A/G]GTAATGACAACAATC | 64326 |
rs537543382 | snp | C/T | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176176313 | CAACACCAGAAAAGC[C/T]AATGCCTACAGCTCA | 64326 |
rs537549603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176188023 | CTTCCCTCCATGAGA[C/T]CAGGCAGATCCAGAG | 64326 |
rs537553723 | in-del | -/CAAAA/CAAAACAAAA | 0.182334 | 0.243435 | intron-variant | RFWD2 | GRCh38.p7 | 1:176093838 | CGAGAGACTCTGTCT[-/CAAAA/CAAAACAAAA]CAAAACAAAACAAAA | 64326 |
rs537559204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176007567 | TCCTTCTAACAGACA[A/G]GACCCTCAGCTGCAG | 64326 |
rs537559688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176141762 | TTAAGACAGGGACTC[A/G]TTTTGTCACCCAGGC | 64326 |
rs537561486 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176058455 | GTTGATCTGTGACCT[A/T]ACCCCCAACCCTGTG | 64326 |
rs537575342 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176009044 | GACTGGGGCTCTCTG[A/C]AGTTTTTCCTGGATA | 64326 |
rs537599189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176121294 | GAGCAACCAAAATTG[C/T]TGTGGCCCCAATTTT | 64326 |
rs537605343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175994809 | TGGGAGACTTTAACA[C/T]GCCACTGTCAACATT | 64326 |
rs537617769 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175969705 | ACTTACAGAGGTCTC[C/T]GTCATGAATCAAGCC | 64326 |
rs537625746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176070711 | GACTGGAGTGTAGTA[A/G]TGCCATCATAGCTCA | 64326 |
rs537637814 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175990596 | TTTTTCAACAACTTC[A/C]GTCAAAATATCTGTT | 64326 |
rs537639641 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175947742 | AAGTGTAAGTTTTAA[-/T]TAAAAGAATAAAGTT | 64326 |
rs537645883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175945640 | TAGCCAATCATCTAG[C/T]GTCCAGATACTTTGT | 64326 |
rs537647760 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176024214 | CAGTGAGCCAATATC[A/G]TGCCACTGCACTCCA | 64326 |
rs537671766 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176080629 | AATAAGGCAATATTA[C/T]GAATAATTGTACGCC | 64326 |
rs537686208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176121787 | AAGGACACAAATTTT[A/G]TATAAATAAATGTCA | 64326 |
rs537712433 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175962748 | TTCCTTCAGCCATCT[C/T]TCACCGCACCTCCCC | 64326 |
rs537727235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176182620 | TAGATCACCTAATTT[C/T]CCAGAATAATCATAA | 64326 |
rs537731620 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-5-prime, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207137 | TTTTTTTTTAAGGCA[A/G]CCACACAACAGCGTC | 64326 |
rs537760468 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176127370 | CATCCACCTCTAATC[A/T]CTGTTAACCACCATA | 64326 |
rs537771125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176132015 | CTTCATGAAATCTAG[C/T]ATGTTTTACGAGATC | 64326 |
rs537772309 | snp | C/G/T | 6.62387e-05 | 0.00575462 | missense, intron-variant | RFWD2 | GRCh38.p7 | 1:176135070 | TCACTGACAGGAGAG[C/G/T]ATAAGCCACTCATTT | 64326 |
rs537773890 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176035507 | ACAAAGTAGTTTTCA[C/G]AGGAATATTGACAGG | 64326 |
rs537775889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176042224 | TGCAGTGAGCCGAGA[C/T]TGCGCCACTGCACTC | 64326 |
rs537782517 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176087525 | ATCATCATTGGCCAT[C/G]AGAGAAATGCAAATC | 64326 |
rs537810567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176123425 | GGTACCCCCATTTCT[A/G]ACCTCCTAGAATCAA | 64326 |
rs537812287 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175949287 | GAATCAACACTTCCA[C/T]ATTCGGGGTGGGGGG | 64326 |
rs537824741 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176075190 | GCACCCCATAATCTG[C/T]TGCATTTTCAAATTT | 64326 |
rs537831125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175967853 | CCAATGTGGCCCCTT[A/G]GAAGAATAATATTTC | 64326 |
rs537842071 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175960252 | TTTGGAGTCTGAAAG[A/T]TTTCAATTCAAAGCT | 64326 |
rs537849074 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176096776 | GATTTATATTGGTCT[G/T]AAGCTGTAGCCAATC | 64326 |
rs537857405 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176090807 | AGACTCAGAAGAAAA[G/T]ACCAAGAAACTAAAG | 64326 |
rs537863211 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176064779 | CTGCCTCAGCCTCCT[A/G]GGCCCAGCCAATTTT | 64326 |
rs537875851 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175996214 | CCTTTGTGCTAAAAA[A/C]TCTCAATAAATTAGG | 64326 |
rs537893389 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176124126 | TTTTTTAAATTTTTA[A/G]TGTTTCTGGGTATAC | 64326 |
rs537897547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176115968 | TCAACGTAATGAAGC[A/G]TAATTCAATGACAGA | 64326 |
rs537898199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176205059 | TGAATGACAATGATC[A/G]ATTCCTTATTCCTCA | 64326 |
rs537898900 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176007098 | CTTCATTTCATTCAT[A/C]TTCCATCGCTGATAC | 64326 |
rs537903457 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176088948 | TGAAGTGAGCTGAGG[C/T]CGCACCATTGCACTC | 64326 |
rs537910766 | in-del | -/T | 0.00597247 | 0.0543191 | intron-variant | RFWD2 | GRCh38.p7 | 1:175962079 | TTATGGATAACAAAA[-/T]GTCAGTGACTGCCTT | 64326 |
rs537920208 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175959366 | AATGATAACATCTTT[A/G]AAAGCTTTCCCTTTG | 64326 |
rs537921309 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176055181 | GCTCAAGCCTGTAAT[C/T]CCATCACTTCGGGAG | 64326 |
rs537923803 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176032327 | AATACAAAGATGTAA[A/C]CTTTAATACTGTTTA | 64326 |
rs537947268 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:175995148 | TCCTGAATGACTACC[A/G]GGTACATAACGAAAT | 64326 |
rs537961302 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175995574 | CGGGATATCACCACC[A/G]ATCCCACAGAAATAC | 64326 |
rs537962128 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176002415 | ATAGTGCAGGTTAGT[C/T]ACATATGTATACATG | 64326 |
rs537968081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175974401 | TTCATGTGATAGTAA[A/G]TCAATGCAATAGACT | 64326 |
rs537982982 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176048620 | GGACAGAGTTATTAT[A/C]AGAACTGAAATCCTG | 64326 |
rs538007645 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175981045 | TACAGAATATATATA[C/T]GTTCCCTTACCTAAC | 64326 |
rs538012654 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:175993356 | CCTCCTCCAAAGGAA[C/T]GCAGCTCCTCACCAG | 64326 |
rs538019626 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175988248 | AATTTCAATAACAAA[A/C]ACCTGTTAAAAAGTT | 64326 |
rs538025075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176019973 | GGAAGAAATATGTTG[C/T]CCTAATTCTTCCGTG | 64326 |
rs538026645 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176019203 | GGTGTGGTGGTTCAC[A/G]CCTGTAATCCCAGCA | 64326 |
rs538034146 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176028263 | TTAGTTTCAATGTCA[A/G]AAATCAATATAGATA | 64326 |
rs538047441 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176186355 | TACAAAAAAAAAATT[A/T]AAAAAAAAAACACAA | 64326 |
rs538081269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175972534 | CAGTGGTGTGATCTC[A/G]GCTCACTGCAACTGC | 64326 |
rs538088103 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176118907 | TACCCTCATAAACAT[G/T]TACAAAATATTACGT | 64326 |
rs538088858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176012584 | TGACCTAGGTCTTCA[C/T]ATTCACTCACCACTC | 64326 |
rs538089554 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207243 | CGGTCCCTGTAGCAG[C/G]CAACCCCGGCGCGCC | 64326 |
rs538103402 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175995721 | GAATCTCTGAATAGA[C/G]CAATAACAGGCTCTG | 64326 |
rs538108782 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176026612 | CATCTACTTGTTAGT[C/G]CATGTCCTCCTTAAA | 64326 |
rs538128802 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176154848 | GTATTGGAAAGAAAA[C/T]TGAAAAATCCATAAT | 64326 |
rs538134375 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176157354 | ACAATCAATTTCAAA[G/T]GACTAAACACATGCA | 64326 |
rs538135266 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:175997526 | CTAATATCCAGAATC[G/T]ACAATGAACTCAAAC | 64326 |
rs538141926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176110047 | TAACACACAGGTACT[C/T]AGAGGAGTCTTCATT | 64326 |
rs538149294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175997795 | AACACTTTTACACTG[C/T]TGGTGGGACTGTAAA | 64326 |
rs538195074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175987284 | TCTTGGACAAAAGCT[A/G]TACTTTACTAATCTA | 64326 |
rs538208121 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176120352 | TTGAACCCAGGAGGC[A/G]GAGGTTGCAGTGAGC | 64326 |
rs538212666 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992359 | TCCATCTGAGGTACC[A/G]GGTTCATCTCACTAG | 64326 |
rs538220392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175990141 | CAAATTGTGATATGA[C/T]GTGTTTCCATTTTCA | 64326 |
rs538231664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176072647 | TCTAGAGATGTCTTT[C/T]TAAGTATAAATTTAA | 64326 |
rs538245429 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176030634 | TATAATTTTCAATAT[A/G]TAAGATATTAGAATT | 64326 |
rs538257908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176023580 | AAAATTAGCTGGGAG[C/T]GGTGGCATATGCCTG | 64326 |
rs538264240 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176128371 | ATTGCCATGGAAGTT[C/T]GCTTCCTGTGTTTTG | 64326 |
rs538289922 | snp | G/T | 0.00914312 | 0.0669923 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176208672 | TGAGAATTACATAAT[G/T]GTTTTTAAACCGTTA | 64326 |
rs538294048 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176120916 | GAGAAATTTTTAATC[A/G]ATGAGCAAAAATAAA | 64326 |
rs538321606 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176178133 | GAAGGAAATAACATA[C/G]TAAATCTTTATTTTC | 64326 |
rs538337502 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176175439 | TTTCAGGATGAAACT[C/G]TTCCACCTCAGATTA | 64326 |
rs538343103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175993674 | ATGAATGAAATGAAG[C/T]GAGAAGGGAAGTTTA | 64326 |
rs538369017 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176040471 | ACCTGTGCGCACCAC[C/G]ACGCCCAGGTAATTT | 64326 |
rs538378154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176126372 | ATATATGGCTTTTAT[C/T]ATGTTGAAGTGTGTT | 64326 |
rs538401624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175973485 | ACTGCATGCAGAGCT[A/G]CAAGTTGCTAAATGT | 64326 |
rs538405051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176110660 | ACAAAAAACAAAAAA[A/G]CAAAACAACAAAAAA | 64326 |
rs538411430 | snp | A/C | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176177115 | AACATCAATCCAATG[A/C]AATGCTATACAGCCA | 64326 |
rs538416963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176152570 | CTTCTGCCTCGGCCT[C/T]CCAAGTAGCTGGGAT | 64326 |
rs538426529 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176062111 | GTTCACGTCATTCTC[C/T]TGCCTCAGCCTCCCG | 64326 |
rs538426730 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176017134 | ATCTTATTAAATGTT[A/C]AATGAATATTTCACT | 64326 |
rs538429855 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176108140 | GATACATCAATTTTT[A/T]AATTTTGCTAATTGT | 64326 |
rs538434017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176149142 | TTTTCTTTAACACCA[C/T]AGCATAAACAGTATG | 64326 |
rs538444495 | snp | A/C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176123212 | AGAAATACTTAGAAG[A/C/G]AGCATTCCAAAAACA | 64326 |
rs538456621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176101406 | CCAGGACTCCTTTGG[A/G]AAAAAAAAGGCTTTC | 64326 |
rs538456997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175973880 | GAGCAGCAAGATCTA[C/T]AGCACAAAGATGAAA | 64326 |
rs538475494 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176199227 | GAGGTTAAGGCAGGA[C/G]AATTGCTTGAACCCA | 64326 |
rs538476851 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176191953 | CAATAAAATATTTTT[A/T]AAATAAGGATTCTAA | 64326 |
rs538496128 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176094406 | AATAGAAATGTGCTA[C/T]GTATGCAGAGATAAA | 64326 |
rs538512000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176016383 | AGTTTTTCCAGAAGT[A/G]AGTGGTCAACAGTGT | 64326 |
rs538542591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175983790 | ATGAGGAACTTGCTG[A/G]GAAATAGAGCAAAGA | 64326 |
rs538547876 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176024483 | GGAACAGATAAAAAA[C/T]TACTCAAACTGATAA | 64326 |
rs538562092 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176159494 | AAATGTGCACACATA[A/C]CCTAATGCGAGCACA | 64326 |
rs538579053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992047 | GTATTGTGTAGTATA[C/T]GTAATCGTATGTGCT | 64326 |
rs538585856 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176069497 | ATTTATCCTCCAATC[C/G]AGTATTCCTCAGGTA | 64326 |
rs538586571 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176192722 | GAGCTATAAAAACAG[G/T]AATTTCTATTACAGT | 64326 |
rs538591143 | in-del | -/AA | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176068620 | TTAAGCTAGATAACT[-/AA]GAGATAAAAGCACAT | 64326 |
rs538597268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176156311 | AGAAGTACATGAAAA[A/G]TAGAGAAGATAAAAT | 64326 |
rs538598441 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176096449 | GAGTGCAGTGTCCAA[C/T]GACCACACAGGGCGG | 64326 |
rs538605331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175977189 | AGATCCTGAAGATAA[A/G]TAAAAGTATGACCAA | 64326 |
rs538617943 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176193519 | TGGAAACAGCCCAAA[C/T]TGTCCATCAACTGAA | 64326 |
rs538618717 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175947841 | AGCCAAAAGAAACAA[A/C]GACTGAAATAAAATG | 64326 |
rs538627954 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176200996 | TGCCCAACTTAAAAA[A/G]CATTTTATTTGGTAT | 64326 |
rs538636511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176154435 | AAATGTGGTGTACAT[A/G]CACGATAGAATGCTA | 64326 |
rs538637784 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176064758 | TCCCAGACTCAATCG[A/G]TGCCCCTGCCTCAGC | 64326 |
rs538660074 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176122583 | TTCAAACAACAGACG[C/T]TATCACAGTGTTTCA | 64326 |
rs538668173 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176049579 | CAAACAGGTCCCCCC[A/C]CTCAAACCACCTTTT | 64326 |
rs538670364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175968809 | TTTCCAAAGTCTTCT[C/T]GCCAACTGGCCCTAA | 64326 |
rs538670566 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175975978 | ATTTGTTTTGCTATC[A/G]ATGACATTTCATGCT | 64326 |
rs538673459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176202151 | AACTGTTACTGTCTT[C/T]ATTACGACAGATTCT | 64326 |
rs538678514 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176194318 | ATAATTATGTTAAAA[C/T]GTAAACAGTCCAGCT | 64326 |
rs538722141 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176021941 | CATACTTGTTAACTT[A/T]CGTGTTCACATCTTT | 64326 |
rs538749836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176063853 | TCGTTAAACCAATGA[C/T]GGATTGTCTACTATA | 64326 |
rs538749886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176071970 | AAGAAGAAAATTTTA[A/G]GGTAGAAGTTATGAG | 64326 |
rs538753857 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176100226 | GAAACCCCGTCTTTA[C/T]TAAAAATACAAAACT | 64326 |
rs538798224 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | RFWD2 | GRCh38.p7 | 1:176203315 | GCACTCCAGCCTGGG[C/T]AGCAGAGCGAGACTC | 64326 |
rs538805362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175982544 | ATAATATTTTCTTTT[A/G]TCTAGCTTATGTGGG | 64326 |
rs538806624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176156955 | GTAATTTCAGCACTT[C/T]TGGAGGCCAAGGCAG | 64326 |
rs538819241 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176045459 | AAGATAAAAAAGGTT[C/G]AAGGATGGCTATTTT | 64326 |
rs538827401 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176058662 | GAAAACCAGAGACCT[C/T]TGTTCACTTGTTTAT | 64326 |
rs538829692 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176141409 | GGGAGGGTGAGGCAG[C/G]AGAATCTCTTGAACC | 64326 |
rs538832670 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176072895 | ACCTCCTTATAGGAA[C/T]AGGGATACACAGTGT | 64326 |
rs538852952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175962987 | CATTTTTTTTAATAT[A/G]TGAGGGCAAACTTAA | 64326 |
rs538861630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176059696 | CCATGTTAGTCAGGC[C/T]GGTCTCGAACTCCTG | 64326 |
rs538867111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175955335 | CTAAGAATAGAAAGG[A/G]ACTTCTTCAAGGTGA | 64326 |
rs538880444 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176155631 | TTCGCTGCCAAAAAA[C/G]AAAATAAAATAAAGA | 64326 |
rs538880896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176181626 | GGCGGGCGGATCACA[A/G]GGTCACGAGATCGAG | 64326 |
rs538885626 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176042960 | CTTGAACCCGGGAGG[C/G]AGAGGTTGCACTGAG | 64326 |
rs538888922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176073121 | TCTCAGTTTTTTTCA[C/T]CTGTAAAATGAGGTT | 64326 |
rs538890346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176024086 | AAGATGGTGAAACCC[C/T]GTCTCTACTAGAAAT | 64326 |
rs538905813 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176163705 | ATCCTAAACAATCGC[A/C]TTTTAAGAAAAATCA | 64326 |
rs538906207 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176179212 | GGAAAATTGCTTGAC[C/G]CTGGGGGGCAGAGGT | 64326 |
rs538935159 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176066438 | TGAACTCCTACTAAA[C/T]TCCTTCCAGTGATAA | 64326 |
rs538941728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176187202 | TGATCATGACTCACT[A/G]CAACTTCGACCTCTT | 64326 |
rs538956285 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176050727 | CCATAACATACATAA[C/T]ACTTGAGATGTGTCA | 64326 |
rs538966986 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176206301 | TCCACCTCTTCCCTC[A/G]TCATTCGTTAAACTC | 64326 |
rs538973241 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175984480 | TTTGCTGCAAGGGTG[A/G]GCCCCTCATGGAGAA | 64326 |
rs538977482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176050883 | CTGGTTCCAGAGTCT[A/G]TGCTCTCAATCATCA | 64326 |
rs538985189 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175983179 | AAAAGAAAAGAAACT[C/G]ATGGCTTAAAGGAAT | 64326 |
rs538990621 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176157062 | AATTAGCCGAGGGGG[A/G]TGGTGTGTGCCAGTA | 64326 |
rs538995769 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176106055 | TGTTTTTTTGAGACA[C/G]AGTCTCGCTCTGCTG | 64326 |
rs538999601 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176022568 | GACAGGCTACATTTT[A/T]AAAAATGTTTCAATT | 64326 |
rs539009319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175972744 | ATGCTGAAACTACAG[A/G]TGTAAGCCACTGCTC | 64326 |
rs539014987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176014321 | CTCTCATCAATGCAA[A/G]TTCAGAGAAAGTGAT | 64326 |
rs539024977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175980459 | AATAAAATTTAATGA[C/T]GTAACTGAAAACAAA | 64326 |
rs539038858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176102898 | GACAGCTTCAATTCC[C/T]CATGATTTCATCTCT | 64326 |
rs539054072 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176153814 | GAGGGCTGAATTTTG[C/T]TGAAAGTCTTTTCTG | 64326 |
rs539066461 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175973284 | TGGAAATACATTGAG[A/C]ATTTAAAATAAAAGA | 64326 |
rs539070591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175965926 | TCCCCTTATTTGACC[A/G]GAGTGTTTCTTTACT | 64326 |
rs539074223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176054604 | GGTCTTTCTTGTCAT[C/T]CCGAACGATGTGCTC | 64326 |
rs539078903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176007988 | CTGCTCTGCTAGCAA[C/T]CAGGGAGACTCCGTG | 64326 |
rs539093620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176161350 | TCCCAGCACCCTGGG[A/G]GGCTGAGGTGGGAGG | 64326 |
rs539113385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176067797 | CCTACAGATGGCAAA[A/G]CCAAAACAGCATTCT | 64326 |
rs539117784 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176165832 | TGTGAAGGGCCTGAA[C/T]TGCAGATACCTTACA | 64326 |
rs539119281 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176112068 | CTTTTAATCATCTAT[A/C]AATTATTCTAAGTTG | 64326 |
rs539119612 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176158097 | AAAACACAAAGGGGG[A/G]AAAAAAAAACCTCTA | 64326 |
rs539132966 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176200188 | GATTAAACAAGTAAC[A/G]TAAAACCTTTAAAAT | 64326 |
rs539134292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176125897 | GTCTTCTTCAATTTC[C/T]TTCATCAGTGCTTTA | 64326 |
rs539150620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176060422 | AAAGAAAATATATTT[C/T]TGTCCCCAAAGTTAC | 64326 |
rs539152792 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176197072 | TCAGAATTTGCATTT[G/T]AAAATAAAGCCTTTA | 64326 |
rs539153488 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176172696 | TTATGCAAATCATGC[C/T]GTCTTAAGCTGAAGC | 64326 |
rs539154884 | snp | A/G | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176185767 | CTTTGGATTGTCTCC[A/G]CTGGACTTCACATTA | 64326 |
rs539160385 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176136282 | TATGGCAATAAAACA[C/T]TGTAAAACAAATTTA | 64326 |
rs539161102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176068401 | ACAGGATTAGAAACT[C/T]TGAGAGTGGAGCCCA | 64326 |
rs539178807 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:176102321 | CGTGCCTGCAAGCCT[A/G]ATCTTTCCCATTCGT | 64326 |
rs539196335 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176077963 | AAAAATCTCTACAAT[A/G]AGAACACAAAGCCCT | 64326 |
rs539199243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176151023 | GAGTATAACCAATTA[C/T]ACCAAAATGTCTAGC | 64326 |
rs539205904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176185024 | TAAGAAAGCTCTACC[A/G]TCGTTTTCCATCACA | 64326 |
rs539214236 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176134870 | GAAACAGATGGGCCA[C/T]ATGAATATCATTTCT | 64326 |
rs539214671 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176133188 | CACATACGTATATAC[A/G]TACGTATATGTACGT | 64326 |
rs539218419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176178252 | GGAAAAAGGAAATGA[A/G]TTAACATTACCAGGA | 64326 |
rs539227108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175963538 | AGCGTCAATTTCACT[C/T]TTAAAGGAACTCAAG | 64326 |
rs539248169 | snp | A/G | 1.6671e-05 | 0.00288708 | intron-variant | RFWD2 | GRCh38.p7 | 1:176043860 | TTTACATAAAAATAA[A/G]TAACAATGGGATAAA | 64326 |
rs539261467 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176089669 | GCTTCACTCTGAGAC[C/G]TAAACTCTGAGTTTT | 64326 |
rs539266120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176041052 | AAAAGGTCAATTAAA[C/T]TGGCAAAAAGTGATG | 64326 |
rs539277136 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176133125 | CGTATATATACTATA[C/T]ATACCCATACACATA | 64326 |
rs539285279 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176002293 | TTGTATTCTTTACAA[C/T]GGATAATCACAACTG | 64326 |
rs539306714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176147772 | GGCCACCACATCAAA[A/G]GCCAAATGAAGATCA | 64326 |
rs539312964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176000441 | ATTTAACTGGGAGCA[C/T]AGAATTGTTTACACT | 64326 |
rs539344774 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176141056 | ATCATTGGTACTCAA[C/G]TGACTTTCATTAGTG | 64326 |
rs539345925 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176191816 | AAGTGATTCCTCCCT[A/C]ATCTGTCTCCATCAA | 64326 |
rs539352161 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176108982 | CTGGGCGCGGTGGTG[C/T]GCACCTGCAGTCTCA | 64326 |
rs539352756 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176008446 | GTTATGATACTTTCA[A/G]CAACAGAATTATTTG | 64326 |
rs539355912 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176145484 | TACACATATCCTATG[A/C]CTCATCAATTCCACT | 64326 |
rs539359515 | in-del | -/TCTC | 0.00119737 | 0.0244387 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207690 | GGGAAGAAGGAGCTG[-/TCTC]TCTCTTCTGAGGGGT | 64326 |
rs539373788 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176184124 | AAAATATATAAATTC[A/G]GTATTATGTAAATTT | 64326 |
rs539374959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176089027 | ATCTATTTAGGCCGG[A/G]CGTGGTGGCTCACGC | 64326 |
rs539378193 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176097537 | ATATGTGTTGTGTGT[A/G]TGATGTCTATAAAAA | 64326 |
rs539380907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175966424 | CTGCATGGCAACCCA[A/G]TGAGGAAGGTACTAT | 64326 |
rs539388272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176197651 | AGGTCCAAAAAATCC[C/T]TTTAAACAATTACCC | 64326 |
rs539398167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176151616 | CTAAATTTTGTTGTA[C/T]TCTAAAAGAAAAAAT | 64326 |
rs539414612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176109827 | TCAATTTATGTTGTA[C/T]ATGGGCTTTTTTTTG | 64326 |
rs539423105 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176085094 | GTAATAAAAATATCA[C/T]ATGCTATCACATCCA | 64326 |
rs539430536 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176103478 | GCATGCCCAGAGAGG[G/T]CATGGAAGCTCTGCA | 64326 |
rs539440082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176135171 | GATATATTCCTTTCT[A/G]TTCCCAGGTTTTCAT | 64326 |
rs539440232 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176115610 | AAAAATTAGCTGGGC[A/G]TGGTGGCGCGTGCCT | 64326 |
rs539445915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175957593 | AAGTGACCAATGAAT[A/G]TAATACAACAACTAT | 64326 |
rs539460564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176038854 | AAAAGATAGATACAC[A/G]GATCAATGCAGAGTC | 64326 |
rs539473161 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176006324 | CAGTCTGTGTCTTTT[A/C]ATTGGAGCATTTAGT | 64326 |
rs539476455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176128143 | GCACCTAATCCAATA[C/T]ATGATTTACAAATAT | 64326 |
rs539479811 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176018749 | TCGTGGCACGCTCCT[C/G]TAGTCCCAGCTACTT | 64326 |
rs539481603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176011352 | TAGAAAATAACTAAA[C/T]CAATGAATAATCTAC | 64326 |
rs539502130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175985794 | AGGAAGGGTTGGTCC[A/G]AATTACCTAGTCTGT | 64326 |
rs539504918 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176005294 | TTTGTTGATCCTTTC[A/C]AAAAACCAGCTCCTG | 64326 |
rs539515824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176142392 | TATTAAATAAATGGC[C/T]TAAATACACAATTAA | 64326 |
rs539516632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176109193 | TGCCCTAATTATGAC[A/G]CCTTTCTCAATTTGG | 64326 |
rs539527609 | in-del | -/AAC | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176169363 | TACTACTAATTAAAT[-/AAC]AACATAGGAAACATA | 64326 |
rs539566994 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176000373 | CTTTTCTCCAGTGTA[A/T]GTTCTTGGCAAGTTT | 64326 |
rs539584684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176044885 | GACAGCACATTTAAA[C/T]TTTCTAATCCACGTT | 64326 |
rs539587457 | in-del | -/AGTA | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176177585 | TCAGGTTTCTATAAT[-/AGTA]AGTATTACTGGTAAC | 64326 |
rs539614146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175985228 | ATAATTTCAATATTT[A/G]GAGCTGCTGTGACTG | 64326 |
rs539616835 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175959403 | AACAAGTCAACGATG[C/T]CAGATACCATTACTT | 64326 |
rs539629494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176024926 | TATTGATGATAAAAA[C/T]GGCAAAGATAGTTAA | 64326 |
rs539642479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176178937 | CCTAGCACTTTGGCA[A/G]GCCAAGGTGGGCAGA | 64326 |
rs539675703 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176204177 | CTCATTTTGTCCTTA[C/T]CTGTCCAACGACAAA | 64326 |
rs539699411 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176006676 | ATGTTGAATATTGGC[A/C]CCCACTCTCTTCTGG | 64326 |
rs539706776 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175983558 | GACTAATACAGAAAA[C/T]TGGTACCAGAAGTGG | 64326 |
rs539730659 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176170762 | AGTCAGCCTGTCCTT[C/G]GAAGCTTTGAAGGCA | 64326 |
rs539737323 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176168205 | TGGGATTACCGGTGC[A/G]CACCACCACACTTGG | 64326 |
rs539748177 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175949824 | AGAGAAGGAATGCAG[A/G]GACCTGGTGAAGATG | 64326 |
rs539753875 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175986472 | TATAAATGTATTTTG[C/T]AGACAGCAATTCTAC | 64326 |
rs539755585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176047427 | TAAGTGGCTGAGGTG[A/G]GATTCAAACACAAGG | 64326 |
rs539760378 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176121997 | TACAAAAAATTAGCC[A/G]GGCATGGTGGCGGGC | 64326 |
rs539791018 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176164645 | AAGAATAGCCAGCCA[A/G]AAGACCAAGGTATAT | 64326 |
rs539797972 | in-del | -/TTTCT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176056794 | TGACCATCTGATTTC[-/TTTCT]TTTGTTTTCTGTGTT | 64326 |
rs539811508 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176196171 | ATTGAAAAGAGGGCC[-/A]AAAAATCAATGATCT | 64326 |
rs539826982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175958231 | ACACAAGAACAAATA[C/T]GTATTTTATAAGTTA | 64326 |
rs539837571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176070419 | TGTAATCCCAGCACT[C/T]TGGGAGGCCGAGGTG | 64326 |
rs539838922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175965390 | TGTTAAGTGATACTA[C/T]TCAATTGTCCAATTT | 64326 |
rs539848974 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | RFWD2 | GRCh38.p7 | 1:176167386 | GTGGTCCCTGACGCA[C/T]AGTAGGCGCCTGGTA | 64326 |
rs539849621 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176000740 | GTTGCTTTTTTTTTT[G/T]TTATGTCATTTGCTC | 64326 |
rs539850229 | snp | C/T | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176177660 | CTGTAAAAATCATTC[C/T]CACAGAGAAAGTACC | 64326 |
rs539850951 | snp | C/T | | | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207380 | GGGGTCGGGGCTCCC[C/T]GGCGAAGGGAGTCTG | 64326 |
rs539854641 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176087582 | ACCAGTTAGAATGGC[A/G]ATCATTAAAAAGTCA | 64326 |
rs539877631 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176118069 | GCATGGGAGGTACTC[C/T]AAGTAGTACACAGTT | 64326 |
rs539883310 | in-del | -/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175997949 | AAAGACACATGCACA[-/C]ATTATGTTTATTGCG | 64326 |
rs539904833 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176131136 | CACAAAAACAATAGG[C/G]TGGGGCTAGGCAATT | 64326 |
rs539920159 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176182239 | CATAAAAAGAGGAGG[A/C]ATTGAAGGAGTAAAA | 64326 |
rs539922739 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176155083 | AGCACTGGCATCACA[A/G]ACAACACTTTCACAG | 64326 |
rs539929045 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176094744 | AGATAAAAGAGCAAA[A/T]TAGATGATCATACAA | 64326 |
rs539932919 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176124605 | AATAACAGAATCTTA[C/T]TCATTTTATGGCTGA | 64326 |
rs539935118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176189378 | TCTAGGGACAGTATT[A/G]TGTTTCTTTTTCCGT | 64326 |
rs539935782 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176053019 | TGGGGAAAAAAAAAA[A/C]CCCTTCTATATGTGT | 64326 |
rs539940460 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176131640 | ATAAAGCTAATAATT[A/C]TGAAAGAAAAAAGAT | 64326 |
rs539943727 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:175996246 | TTTGATGGGATATAT[C/T]TCAAAATAATAAGAG | 64326 |
rs539972937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175972138 | AACAACAACAACAAC[A/G]AATACAAAAGGTGGT | 64326 |
rs539976462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176166982 | CCTACAACAAACAAT[A/G]GTTACCTATGGAAAA | 64326 |
rs539976655 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176166450 | AAGCCTGTAAAGGCC[A/G]CAAAATTAAATTACA | 64326 |
rs540006386 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175974781 | CTCAGGCCTGTAATC[C/T]CAGCACTTTGGAAGG | 64326 |
rs540009757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175991942 | GCTGTTGTATAGTAA[C/T]TTAAAAAAACAAGTG | 64326 |
rs540014676 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176129094 | AGCTATTATGCAGTA[C/T]TGTTTCTTAAATATC | 64326 |
rs540022876 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175946876 | TCTATCTACTGAAAG[A/C]CCTGTGGGAGAGTTG | 64326 |
rs540045601 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176189174 | GAATAAAGATAAAAA[C/T]GGAAACAGACTTCTC | 64326 |
rs540072388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176025530 | AAAAATGGTAACATA[C/T]ATAGGAAAAAAAATT | 64326 |
rs540077840 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176115519 | TTGGAGAGGTCAAGG[A/G]GGGAGGATCACGAGG | 64326 |
rs540086219 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176030609 | AAGTCACAACATTAA[C/T]CACCATGATTATAAT | 64326 |
rs540090070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176088036 | ATATGTTCTCACTCA[C/T]AGGTGGGAACTGAAC | 64326 |
rs540094995 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:175949799 | TTTGGGTCTAGTCAC[A/C]TTTTAATATAGAGAA | 64326 |
rs540115040 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176070845 | TTTTGTAGAAATGAG[G/T]TCTTGCTATGCTTCC | 64326 |
rs540125982 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176039956 | TAAAACTATAAAAAA[C/T]CTTTAAAAACAAAAA | 64326 |
rs540132215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175994822 | CACGCCACTGTCAAC[A/G]TTAGACAGATCAATG | 64326 |
rs540140852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176129046 | CATAGAATGACATGG[A/G]TAAACTAGAGGAATT | 64326 |
rs540146228 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175995074 | CGCAATCAAACTAGA[A/C]CTCAGGATTAAGAAA | 64326 |
rs540146246 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175991544 | GTAAAAAAGTGTTCT[A/C]CCTTCAGAAATAAAT | 64326 |
rs540149647 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | RFWD2 | GRCh38.p7 | 1:176104044 | AACATATCATAAAGC[A/G]TCTACAATAAAGGAA | 64326 |
rs540153189 | in-del | -/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176025894 | ATAAAAACAAAAAAA[-/C]CAAAAAAAAAGAAAA | 64326 |
rs540155610 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176104000 | AAGAGAAGCTAAGAT[-/A]GGGGAAGAAGAGAAG | 64326 |
rs540169676 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176101594 | CAGAAGCCCAACATG[A/C]CAGCAAAGGGTAAAA | 64326 |
rs540174966 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176171232 | AGATCTTCTGGATAA[A/T]TTGCTACAGCTTCTA | 64326 |
rs540182047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176063350 | CAGGCATGAGCCACC[A/G]CGCCTGGCCCGAAAA | 64326 |
rs540186031 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176161439 | ACAAAAAATAAAAAT[A/T]AAAATAAACTAGTTG | 64326 |
rs540211615 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176206057 | ATAAAAAGCATGTCT[G/T]TATAAGACATCCATG | 64326 |
rs540218484 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176034992 | ACAATTTAAACAGGA[A/C/T]CCAACATCTTACAAT | 64326 |
rs540235187 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175980675 | AATGTCCACCCTAAT[C/G]ACCACTGCTTTTTTT | 64326 |
rs540238360 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175945678 | GAATTAAAGTAGTAT[A/G]CTGTCATAAAAAAGT | 64326 |
rs540244386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176070145 | TGTAAATGATACCCA[C/T]ATTTTCCCTGCCCAG | 64326 |
rs540247321 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176019613 | CACCTGCAATCCCAG[G/T]ACCATGGGAAGCATA | 64326 |
rs540270701 | snp | A/C | 0.000798403 | 0.0199641 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176206871 | CGCCACGGAAGGCGG[A/C]GACGGGGAAGAGGAT | 64326 |
rs540274478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175970975 | GACATAAAGCTGTTA[A/G]AAGTAAATCGAGAGA | 64326 |
rs540301589 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176172923 | AAAACACAAATAGAT[A/G/T]TATCAGGATGAAATG | 64326 |
rs540309226 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176179660 | GAGGATTGCTTGAGC[A/C]CAGGAGATCGAGGGT | 64326 |
rs540323037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176075732 | ACCTCAGGCTGGGTG[C/T]GGTGGCTCATGCCTG | 64326 |
rs540324410 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176185128 | GTGATAAATTTATTA[-/T]TCTAGTTTCGACAAT | 64326 |
rs540327826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176083141 | GTGGTCTGGATATAA[C/T]AGTTAATGATTCTTT | 64326 |
rs540333115 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176205104 | TTTTAGTGTACTTAC[A/G]CGGAGGCTAACATGT | 64326 |
rs540336094 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992710 | GGGGCACCTGCCATT[A/G]CCCAGGCTTGCTTAG | 64326 |
rs540337168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175986721 | GAGATATGCACTAAA[C/T]GCTATGGGTCACAGA | 64326 |
rs540343576 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176026383 | ACTTTACACAAAGAA[A/T]CTTTTTTCCATAATC | 64326 |
rs540344942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176109404 | CTTTCACCACTGATC[C/T]ACATGACCACCTTTA | 64326 |
rs540358955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176076263 | AAAAATCATAATCAC[A/G]CCAAGCATAACTCTT | 64326 |
rs540374972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176197432 | TGAAAAAAAGAAAGG[A/G]AACAGGCCTCAGAAG | 64326 |
rs540377145 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175971228 | GTATTTTGTAGTAAC[-/T]TTTTTTTTGTTGTAC | 64326 |
rs540379592 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176102047 | AACCAGACTGCCCAT[A/C]CTGGATGAAGCCTGC | 64326 |
rs540383823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176105543 | TAAGTGTATTTTGAT[C/T]GTGACAGCTAGGTTT | 64326 |
rs540398106 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176151221 | AAGCGTGTAAGAAAA[A/C]GAATAAAGAGAAATG | 64326 |
rs540402938 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176138307 | AGAAAACACCAATGT[C/T]AAAGAGATGGGCAAA | 64326 |
rs540412610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176069117 | TTGAGCCTAGGAGGT[C/T]AAGGCTGTAGTAAAT | 64326 |
rs540430764 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176048718 | CTCCGCCTACTCATA[G/T]ACATAGCTAATCAAC | 64326 |
rs540442381 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176126489 | TTGAGATGGAGTCTC[A/G]CTCTGTCACCAGGCT | 64326 |
rs540466700 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175950394 | CTAGATATTGGCTTA[A/C]GATAAATTATTTTTT | 64326 |
rs540467395 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176098563 | CTCTGTGTTAACATA[C/T]TGACTAACTTCAAAA | 64326 |
rs540468573 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175978207 | CTTCAAGATTGGCAT[A/T]CACAGAACACTCTTT | 64326 |
rs540474182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176106212 | ATTTTTGTATTTTTT[A/G]TAGAGACGAGGTTTC | 64326 |
rs540480664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176007702 | GGCAGTCTGCCTGTT[C/T]TCAGATCTCCAGCTG | 64326 |
rs540484951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176006898 | TGAACGTTGGCCTGC[C/T]TTGCTAGATTGGGGA | 64326 |
rs540492174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176041385 | CAGAGTCTCGCTCTG[C/T]CATCCAGGCTGTAGT | 64326 |
rs540501580 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176104331 | AATTTTTAAAAATTG[A/G]TAATTTTAACTAAAA | 64326 |
rs540502609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176002440 | TACATGTGCCATGCT[A/G]GTGTACTGCACCCAC | 64326 |
rs540513088 | snp | A/G | 1.6517e-05 | 0.00287372 | synonymous-codon | RFWD2 | GRCh38.p7 | 1:175988313 | ATAATCTCCATTGGA[A/G]GCCAGGCCTACAAAG | 64326 |
rs540513275 | in-del | -/AC | 0.489052 | 0.0731729 | intron-variant | RFWD2 | GRCh38.p7 | 1:176119646 | TATACATTCATACAC[-/AC]ACACACACACACACA | 64326 |
rs540516866 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176024807 | CAAAACAATCAAAAA[A/C]TAAAATTTAAAAGCA | 64326 |
rs540521105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176152608 | TCGCACCACCATGTC[C/T]AGCTAATTTTTGTAT | 64326 |
rs540522561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176199687 | AAAGACTACCGACTA[A/G]AGGACTCCATTAATA | 64326 |
rs540528210 | in-del | -/AT | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176133153 | TACGTATATACGTAC[-/AT]ATATATATACGTATG | 64326 |
rs540533657 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176076487 | AGTGTAGAGAGGAAA[A/G]TTTATAGCACTAAAA | 64326 |
rs540537595 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207346 | CGGGGCTGCGCTCAG[A/T]CGCTCAGGGCGCGCC | 64326 |
rs540544277 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176007243 | TCTAGTTATACATTC[C/T]TCTAAATTTTTTTCA | 64326 |
rs540553020 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176088464 | TAAGGCAAGATGAAT[A/G]TTCCATATGTTCATC | 64326 |
rs540561778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176191984 | ATAACTATGTGCTAG[C/T]TTCAGGGTCAGAAGT | 64326 |
rs540564962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176137460 | AACACTATACCAATT[C/T]AAATTCCTAACGCCA | 64326 |
rs540579046 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176107745 | TTTAATCGAGTGATC[A/G]AAGTTAACATCACCA | 64326 |
rs540592571 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175973046 | CATGTTGGTCAGGCT[C/G]GTCTCAAACTCCCAA | 64326 |
rs540602612 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176051494 | AATGTACAGTACATA[C/T]ACTTGAAAATAAACA | 64326 |
rs540620725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175969935 | CTAGTAGTAATAATA[C/T]TAGTGTATTATTCTA | 64326 |
rs540628007 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176109514 | TTAATAGTTGATGAG[A/G]TAAATTCATCATTAA | 64326 |
rs540656861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176148784 | AGTTATTGCAGTCAA[C/T]CTTACTGATAACTTT | 64326 |
rs540661594 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176191597 | GTAAAAAGGAAAAAA[A/T]AATAATAAACCTCAA | 64326 |
rs540662380 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176103865 | TCCCTGAGATAATTG[G/T]TAAGATAAAGGCAGT | 64326 |
rs540679188 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176040806 | GGCATAACATGATGC[A/G]AAATAAAGCTTCCAA | 64326 |
rs540691077 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176019073 | TGGAAGGCTGAGGCA[C/G]GAGAATCGCTTGAAC | 64326 |
rs540695868 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176188325 | CCTTCCCAAGAAAGG[C/G]ATGAAAAATCTCAGA | 64326 |
rs540706711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175983508 | TTTGTAAATTACCCA[A/G]TCTTGAGTATATCTT | 64326 |
rs540718138 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176166043 | TATACCATTATATTT[G/T]ATTCTCAATAACAAT | 64326 |
rs540725560 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176065094 | CAATAAACTAATATG[A/C]GTTTTAGTCATTAAT | 64326 |
rs540729082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176021915 | AGCTGACAGATTCCA[C/T]CTTCTATATACATAC | 64326 |
rs540733784 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175952335 | GCTGAGGTGGGAGAA[C/T]CGCTTGAACCTGCGA | 64326 |
rs540741870 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176015823 | GATGATGACAAGAAC[A/G]CTTTTAAGTGGAATT | 64326 |
rs540765737 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176124760 | CTCTTTCATGTATAC[A/G]TTTCCTTTCTTTTGG | 64326 |
rs540768711 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175984064 | TGGGAAGAAATTCAA[C/G]CTGGCTGCAGAAATT | 64326 |
rs540779435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176159175 | GCAAAGTAGTAATAT[A/G]CAAAATACAAGCACA | 64326 |
rs540791751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175959609 | GTTTAGCAAGATGGT[C/T]GGATTAAAAATGGGG | 64326 |
rs540811162 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175976509 | TCTCAAACTCCTGGC[C/T]TCAAGTGATCCTCCC | 64326 |
rs540823616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176037871 | TTTCCCCCTAACATC[A/G]GGAACAAAGCAAGAA | 64326 |
rs540824045 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176134747 | ACAAGATATTTAAAG[C/G]TATCATTACTTTAAG | 64326 |
rs540836800 | snp | A/G | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176184772 | CTAGTAACAATACCA[A/G]TGAAATCATATTTCA | 64326 |
rs540837845 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176086750 | TCTTCACAGAACTGG[A/C]AAAACTACTTTAAAG | 64326 |
rs540845401 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175952263 | CCCATCTCTACTAAA[A/T]ATACAAAAATTAGCT | 64326 |
rs540872050 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176145260 | TAGGTGCTCAACCTC[A/C]TAAGTCATCTGGAAA | 64326 |
rs540895054 | snp | A/G | 0.0517044 | 0.152246 | intron-variant | RFWD2 | GRCh38.p7 | 1:175994270 | GGAAAGGAACAACCC[A/G]TACCAGCCACTGCAA | 64326 |
rs540904932 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176133513 | CTACTATGCTATACA[C/T]TGGCCCTTTTAGTGT | 64326 |
rs540911643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176101466 | TCACTGATAAGTAAT[C/T]GTGTCTTTGTACTAT | 64326 |
rs540932612 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176055217 | GACAGGTGGATAACC[G/T]GAGGTCAGGACTTTG | 64326 |
rs540938298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176134156 | AAGTGATAAGGTTTC[C/T]GAAGGTTATTATAAT | 64326 |
rs540940123 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176141928 | TTGTAGAGACAAAGT[A/C]TCACTATATTGTCCA | 64326 |
rs540950549 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175999893 | ATATACCAGTTTGCC[A/G]TTTATATGTCTTCTT | 64326 |
rs540950625 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176005343 | GGGTTTTTTGTGTCT[C/G]TATTTCCTTCAGTTC | 64326 |
rs540952192 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176094013 | GGAGGCAGAGTGAGA[C/T]TCTGTCTCAAAAAAA | 64326 |
rs540966114 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176047937 | ACAATTAGTGAGGCA[C/T]AGTGATGGGTTCTTG | 64326 |
rs540971669 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176160699 | ACTGATCATTAGATA[A/G]ATGCAAATCAAAACC | 64326 |
rs540973867 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175966731 | CATTACATTTCAAAT[C/G]TCATAAACCTAGGCT | 64326 |
rs540976240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175977349 | CCCACTAATCTGCAT[A/G]TCTAGTTAAAAAAAG | 64326 |
rs540981495 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176187258 | AGCCTCTCAAGTAGC[G/T]GGGACTACAGGTGCA | 64326 |
rs541010220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176057993 | CTGGCCGCCCCGTCT[A/G]AGAGGTGAGGAGCCC | 64326 |
rs541035646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175970534 | CATGAGATCAGGAAA[C/T]AGAGCAGTTAAGAAG | 64326 |
rs541040175 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176091704 | AGAACAGGTAACAAT[C/G]GAACCAGAAGAGGGA | 64326 |
rs541040543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176181117 | TAGGCTACAGATACA[A/G]GTAACAGTGGGTTCT | 64326 |
rs541041803 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176108108 | AAATTAAAAAGTAAA[A/C]ATTTTAGGTTTTCTG | 64326 |
rs541047988 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176195898 | AAATCGGGGACGGAG[G/T]GGGTTAGGAGCTGAA | 64326 |
rs541072062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176008739 | CTTTTTGCTATTGGC[A/G]GTGTTGCTGTTTGTG | 64326 |
rs541078657 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176072686 | AGCACTCTACAATAA[C/G]GAACATATTAAAAGT | 64326 |
rs541098188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176023668 | GGTTGCAGTGAGCTG[A/G]GATCGTGCCATTGCA | 64326 |
rs541115328 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176011043 | TTTCTTAATATTCCC[C/T]TTTAAACATGCTTTC | 64326 |
rs541115497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176003893 | TTCTGTGAAGAAAGG[C/T]GTTGGTAGCTTGATG | 64326 |
rs541120279 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176186868 | TTTGCTGATAGATGT[A/T]GGGTATGAGACAAAA | 64326 |
rs541132758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176050271 | ATGTCATTAGTCAAG[C/T]GATTAAGCAGCAAGG | 64326 |
rs541150715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176099345 | GTTAACTAAATGAAC[C/T]GAACTCACCAAAAAC | 64326 |
rs541153191 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175961439 | TAGGGTAGATATCAC[A/G]TGCCAGATAATTGTG | 64326 |
rs541164176 | in-del | -/AA | 0.0115144 | 0.0749975 | intron-variant | RFWD2 | GRCh38.p7 | 1:176005756 | TACATTTGCTGAGAG[-/AA]CTTTACTTCCAACTA | 64326 |
rs541164473 | snp | A/T | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176145492 | TCCTATGACTCATCA[A/T]TTCCACTTCTAAATA | 64326 |
rs541166558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176065773 | AGTGCAGTGGCGCAA[C/T]CTTGGCTCACTGCAA | 64326 |
rs541173883 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:176057616 | TGCCGGGATTGCAGA[C/T]GGAGTCTCGTTCACT | 64326 |
rs541176058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176155815 | TGGTAAAAATGACTA[C/T]TGATTTCATCAGAAA | 64326 |
rs541176457 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176045081 | AAACTACTTCAGTCT[C/G]AATCCTGGCTCCTCT | 64326 |
rs541192937 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176028479 | CTGAGGTGGAATAAT[C/T]ACTTGAGTCCAGGAG | 64326 |
rs541199780 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176196195 | ATGATCTAAGCTTTC[A/G]TACTAAGAAACCAGA | 64326 |
rs541203459 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207730 | GTGCTTCCGAATCGC[A/G]GAATGTAGGTGCTCA | 64326 |
rs541206154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176140551 | AGACATTTTAGTACT[A/G]GTAAATAGAAAAATG | 64326 |
rs541214971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175956808 | TGTAAAATAGGCTCA[A/G]GCAGGTCCTTCAGGA | 64326 |
rs541224270 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176089497 | GTGGTCCTAAATATG[C/T]ATGGTATTTACCTGC | 64326 |
rs541228555 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176087174 | AAGAAAACCTAGGCA[A/G]TACCATTCAGGACAT | 64326 |
rs541229058 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175957654 | TAAACTTACAACTAC[G/T]CTACAATCTCATAAT | 64326 |
rs541238768 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176038535 | AAGTAAAAGAAGAGA[C/T]AGGGCTGGGCATGGT | 64326 |
rs541245504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176176364 | ATATTATTGGCCTGC[A/G]AATACCCTTAATACT | 64326 |
rs541265426 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176201552 | AGATTTGTAAAAGGA[A/C]AAGATAACTGCTTAT | 64326 |
rs541267291 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176208206 | CTTGGGAGGCCTAGG[A/G]GGTCGGATCACCTGA | 64326 |
rs541285059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176072342 | CATTCATTTAACAAA[C/T]ATTTACAGACATAGG | 64326 |
rs541303629 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176051943 | TTTTTAAGTTATAAA[A/C]TAAAAAGGTTACAGT | 64326 |
rs541325352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176086147 | TACAAGACTAAAATG[A/G]GAAACATCTTCACTT | 64326 |
rs541326108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176181918 | AATGAAATTGTATTA[C/T]AATAAGGATCTAAGC | 64326 |
rs541328802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176142523 | AAGGAAAGGAAGACC[C/T]GGTATGAATGCAGGA | 64326 |
rs541338013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176174876 | TAGCTTATTATTCAT[C/T]CCCAAAACATTCAGA | 64326 |
rs541340358 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176052742 | ATTTCAACTTGTGCA[C/T]CTTACTAGTTTCCTA | 64326 |
rs541361498 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175955546 | AAAAAGAAAACTGTC[A/T]TCATTTGCAAAAGAG | 64326 |
rs541365102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175963964 | ACAGTTGTCCAGTTA[C/T]GTGGATTCGTATATA | 64326 |
rs541376119 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176136126 | CTTTTAATTAACCTT[-/A]ACTCCTAGAAATGCA | 64326 |
rs541378244 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176137773 | GGGTTTTTTATAGAC[C/T]TATTAGTATTAGTAT | 64326 |
rs541379805 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176177642 | AGAAATTACAAAGGT[G/T]ATCTGTAAAAATCAT | 64326 |
rs541384141 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176105024 | AAATTGTTAAATAAA[A/G]TACAGAAAAAAAATT | 64326 |
rs541394503 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176141078 | TCATTAGTGCCTTGA[C/T]AAAGATATGCTTAAG | 64326 |
rs541395028 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176202168 | TTACGACAGATTCTA[C/T]GATACGTTCTAGTTC | 64326 |
rs541395585 | in-del | -/A | 0.000726444 | 0.0190445 | intron-variant | RFWD2 | GRCh38.p7 | 1:176081101 | TTCTCAAATTCAATT[-/A]AGATTCTAGACATTC | 64326 |
rs541414222 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175955496 | GGTACAACCCAGTGC[A/G]ACAGTCAAGAAAAGG | 64326 |
rs541426812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175951164 | TGAGACAGGAGAATC[A/G]CCTGAACCCGGGAGG | 64326 |
rs541433121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176081512 | CACTGTGAATTCTCA[C/T]TTTTTTGGCAATAAT | 64326 |
rs541434178 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175950272 | ATGGTCTTTTAGGAC[C/T]GAAATTTAATGAAAG | 64326 |
rs541435645 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176108234 | ACTCTATAAAGTTCA[C/T]ACATTTCTGGCTTCA | 64326 |
rs541443157 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176178291 | TACAAAATTTAACTC[G/T]TTTTTTAAATCAGCA | 64326 |
rs541457125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176036628 | TTACAATGGTGAGAA[C/T]GCAATGTGCATTCAG | 64326 |
rs541458900 | in-del | -/TG | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176090958 | ACACTAAGGTGAAAC[-/TG]TGTTTTTGTCTATAC | 64326 |
rs541476944 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176171626 | TATGAAGTGAGCACA[C/T]GGTAGTGGAAAAGTG | 64326 |
rs541477741 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175958185 | TAAATTATATTTCAA[C/T]AATATCAATTTTAAA | 64326 |
rs541479104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176040559 | AAGCCATCCTCCTGC[C/T]TCAGCCTCCAAAATT | 64326 |
rs541484607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176049484 | TATACTGTAAAAATA[A/G]ATTTTAATAGAAATA | 64326 |
rs541485156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176094920 | CGGAGTACAAAAGCA[A/G]TGAGATCTTCAAAAG | 64326 |
rs541494575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176054208 | TCTGTCACCCAGGCT[A/G]GGGTGCAGTGGGCAT | 64326 |
rs541495776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176008017 | TGGGCGTAGGACCCT[C/T]GGAGCCAGGTGCGGG | 64326 |
rs541535436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175984275 | GTCCTGTGTCCCTGC[C/T]GCTCCAGCCATGACT | 64326 |
rs541551986 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175958633 | ATTTCTCCAAATGTT[A/T]AGCATTACGTTAAAT | 64326 |
rs541572642 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176117143 | TCAAGTTTCCTCATC[C/T]GTAAAAATGAGGTGA | 64326 |
rs541585523 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175965977 | CGCTGCATTTTGAAA[C/T]CAAGTGAGAGTCCAT | 64326 |
rs541588237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175986773 | ATTGCTCTATTACTA[C/T]GCATTTCAATCACTA | 64326 |
rs541589056 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175947395 | TTTTTTTTTGAGACG[C/G]AGTCTTGCTCTGTTG | 64326 |
rs541607310 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176000696 | AAAAGGGTTCTCAAC[C/G]TGTATATGGTAGAAT | 64326 |
rs541640602 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176030108 | AGATGCACACCACCA[C/T]GCCTGGCTAATATAT | 64326 |
rs541641935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176120463 | TTAATAAAGACATCA[A/G]AAAACGTCAAGGGAA | 64326 |
rs541646478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176162682 | AAATAAGTTATAATG[C/T]ATTGAAATTGTTCTT | 64326 |
rs541652797 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176023039 | GTTTCTAGCTTTGTG[C/G]GAGTTGTAGTGAAGG | 64326 |
rs541671624 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176205851 | TGTTATCCAGTATAG[C/T]ACAGTTACATCTGAC | 64326 |
rs541673494 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176018764 | GTAGTCCCAGCTACT[A/T]GGGAGGCTGAGGCGG | 64326 |
rs541711196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176125541 | AGTTCACTGTAGGTG[C/T]GTGGATTTGTTTCGG | 64326 |
rs541724343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175986176 | AGTCACCCGCCACCA[C/T]GCCTGGCTAATTTTT | 64326 |
rs541741322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176037063 | TCAAACAAAGAAAAC[C/T]ACACGCCCAGAAAGC | 64326 |
rs541743617 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176064188 | TTTCTCAATCAAAAT[G/T]ACCTTCCTTGCATAA | 64326 |
rs541744441 | in-del | -/ATA | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176159196 | TACAAGCACACACAC[-/ATA]CACAAATCAGTAAGA | 64326 |
rs541748153 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | RFWD2 | GRCh38.p7 | 1:175995716 | AAATTGAATCTCTGA[A/G]TAGACCAATAACAGG | 64326 |
rs541760673 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992423 | GCAGCGCACCGTGCG[C/T]GAGCCAAAGCAGGGT | 64326 |
rs541762426 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176057280 | ATAATAAGAACTTAA[C/G]AGTGTATTCCCTCCC | 64326 |
rs541815867 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176114262 | GGTATTTTCATGACC[A/G]TTCAGAAACAGATAC | 64326 |
rs541816493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176032167 | ATTCTTCCAGACTCG[C/T]TTCTAAACTACTGTC | 64326 |
rs541822706 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176187640 | TACAGCTTTGTGACT[C/T]TGAGCAAGTAGTTTA | 64326 |
rs541828911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176032965 | AGTTATAAATTATAA[C/T]AACTGTTATCATAAT | 64326 |
rs541830562 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176025079 | TTCAGTGTTAGAAAA[A/C]GCATAAGCACCAATT | 64326 |
rs541835463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175995307 | AGGAAAGATCCAAAA[C/T]TGACACCCTAACATC | 64326 |
rs541878810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176123003 | CCAACAAAATAAGTT[A/G]AAGTTTCAGTTCATT | 64326 |
rs541882021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176144496 | AATACTGTAAATACA[C/T]AGTCTCCCAGATTTA | 64326 |
rs541883088 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176066723 | ATTAATGAATTCAAT[C/G]TCAAATTTCACTATG | 64326 |
rs541909203 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176006400 | GTCATTATGATGTTA[A/G]CTGGTTATTTTGCTC | 64326 |
rs541916943 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:175947850 | AAACAAAGACTGAAA[-/T]AAAATGAAAAAAAGA | 64326 |
rs541921004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176136240 | GAAAACTGAGCGATT[C/T]TTTTTGTCAGTCTAA | 64326 |
rs541928563 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176180044 | TATCTTAGAGCATCT[A/G]CTACTTCACTACCAC | 64326 |
rs541943469 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176046879 | CAAATCCATACCTAA[C/T]CCCCCTCCCCAAATA | 64326 |
rs541949118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176031530 | AAAAGTAAATTTAAA[A/G]GAAAATATCATCTTC | 64326 |
rs541951371 | in-del | -/A | 0.300149 | 0.244919 | intron-variant | RFWD2 | GRCh38.p7 | 1:175950218 | ACTTTATGTGTTAAA[-/A]AAAAAAAAAGTCAAC | 64326 |
rs541953381 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176018636 | TCAATAGGGAAAAAA[-/T]AATTTCATTTATTTT | 64326 |
rs541970411 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176001712 | TTTACTACTTTGTGG[A/C]CTTACATTACAGTCT | 64326 |
rs541999658 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176164266 | AGTTAAGTACTAAAG[A/T]CTTGCATTTGTTCTT | 64326 |
rs542002574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176053482 | TTGCCTAATTGTTAA[C/T]TATTTTAATAACTAT | 64326 |
rs542004485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176151159 | GTCAAAACTTCCAAA[A/G]AACATGTAATGATCA | 64326 |
rs542042467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176060576 | AACTGCAAAATAAAA[C/T]ACATCTAATTTCTCA | 64326 |
rs542051807 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176110134 | CACAATGCAGACGAT[A/T]CTATTTATCTTGTCT | 64326 |
rs542074818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175954806 | ACCAACTACTTTTAT[A/G]AACAGATGTAAAAAA | 64326 |
rs542088680 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176172194 | AGCTAGGACAACAGC[G/T]GCATACCAACACGCC | 64326 |
rs542094968 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992229 | ACAATCTAATTATAC[A/T]TTTTCAGTTATTTAA | 64326 |
rs542103814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176095961 | TTTGCATGTATACCT[C/T]TTTACTATTCTGTGA | 64326 |
rs542105856 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176010702 | GGGAATCTGTCTCTC[G/T]TATTTCAGTTGTTAA | 64326 |
rs542115474 | in-del | -/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176035256 | AATATATAGAAACTA[-/T]TTTTTTTTTAAAAAG | 64326 |
rs542143098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176158147 | CAAAACACTTACACC[C/T]ATAAAAAGAGTATCT | 64326 |
rs542147944 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176166125 | AGCCTGTATTTATTT[A/T]TTTTATTTATTTATT | 64326 |
rs542163437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176150518 | AATGACGACAAAGCA[C/T]CCAAGCCTTCCACAT | 64326 |
rs542175110 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176025931 | CAAATAAAAAAGACA[A/C]CTAATGTAACTGTGG | 64326 |
rs542192650 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175949295 | ACTTCCATATTCGGG[A/G]TGGGGGGCTGGGGTG | 64326 |
rs542207972 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175984696 | AGCCAGGAGGGAAGC[C/T]GTACCCTGCAACGCC | 64326 |
rs542209209 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176164745 | AGAAATTCTTTTCCC[A/G]TGAATCGATACATTT | 64326 |
rs542216748 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176131647 | TAATAATTCTGAAAG[-/A]AAAAAGATTAGTAAA | 64326 |
rs542223810 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176000034 | AGATGAGTAGTTTGC[A/T]AATATTTTCTCCCAT | 64326 |
rs542243728 | snp | G/T | 0.00517822 | 0.0506191 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207369 | GGCGCGCCCTCGGGG[G/T]CGGGGCTCCCTGGCG | 64326 |
rs542281032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176203679 | AGATTCTCCATCAAT[A/G]AAACACTGTTAAAAT | 64326 |
rs542289006 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175981717 | GTGAAAAGACAACAT[A/G]TGGATTGGGAGAAAA | 64326 |
rs542300098 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175994594 | GGCAGGGGTTGCAAT[C/G]CTAGTCTCTGATAAA | 64326 |
rs542310555 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175991119 | CTGAACAGTAAGTAC[A/C]ATAATACATACTTAA | 64326 |
rs542317333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175945745 | GGCTAAGAAAGATCA[C/T]GGAACAGGAGGATAG | 64326 |
rs542319451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176176870 | AGTATATGTGGATAT[A/G]AACAATCTCAACTAC | 64326 |
rs542336248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176080104 | CAAAATGGAAATTAA[A/G]AGGTATTTTGATATA | 64326 |
rs542344474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176028532 | ATCATGCCACCAAAA[A/G]AAAAAAATGAAATGA | 64326 |
rs542349042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176170891 | AGCACTTTGGGAGGC[C/T]GAGACTGGTGGATCA | 64326 |
rs542356385 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176209177 | TCATGACCTCTGAAT[C/T]TATTTTTCAGTGTTT | 64326 |
rs542357480 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176164385 | TGACTTTTTTCCAAG[C/T]GTCAGACTGCCATAT | 64326 |
rs542360075 | snp | A/C | 8.41701e-05 | 0.00648675 | intron-variant | RFWD2 | GRCh38.p7 | 1:175988429 | TGAGGAAAAGTACAA[A/C]GAGTAAGAACTTACT | 64326 |
rs542379010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176080782 | GGTAGTTAAAATTCT[C/T]TTCTGGAAGCTTCAC | 64326 |
rs542379162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176073703 | CTATTGTTTAATAGT[C/T]GAGATACTGTCAAAG | 64326 |
rs542397839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176147948 | CCTGTTGCCCAGGCT[A/G]GAGTGCAGTGGCGCG | 64326 |
rs542405471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176197203 | AAAGCTATGACACAA[C/T]AACAAGTGGCCCAAC | 64326 |
rs542457232 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175962920 | TTATATCCGCAAACA[C/T]AGTTCAAGATTTATT | 64326 |
rs542465968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176067401 | CACCTATAAAAACTC[C/T]GACACCCTAGTGGGC | 64326 |
rs542471401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176154042 | ATCAGTAACACTGGT[C/T]TTAAGTTTCCTTTTT | 64326 |
rs542476322 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175962556 | TGGGGGTTTTCTTTC[G/T]ACGAGATATCCCCCA | 64326 |
rs542487116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176103081 | CTATTGCAATTCCAG[C/T]GTCTTGATAAATCAG | 64326 |
rs542492849 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | RFWD2 | GRCh38.p7 | 1:176187402 | ACACATATAAATATA[C/T]GTGTGTGTGTGTGTG | 64326 |
rs542508724 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175976410 | AGCCTCTTAAGCAGC[C/T]GGGATTACAGGTGTG | 64326 |
rs542515973 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175978533 | CTTCTTATTTCCTTC[C/G]TTTTCTACTTCCCCA | 64326 |
rs542521306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176014584 | TCATAATAAAATACA[C/T]GTTTTTTTAAAAATT | 64326 |
rs542541798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176204253 | ATTAAAAATAAGTTA[C/T]ATATAACATCACAGA | 64326 |
rs542542673 | snp | C/T | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176145745 | ATAAAAGATTACATA[C/T]TGCACAAGCACACTT | 64326 |
rs542559151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176154598 | TGAGGACACATGGAC[A/G]CATAGAGGGGAACAA | 64326 |
rs542574326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175988846 | CCAAAAAAAAAAAGT[C/T]TTCTTTTCAACATAT | 64326 |
rs542580943 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176104610 | CTGAGATATATTTCT[C/G]ACCTAATATATTGGC | 64326 |
rs542601270 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176029316 | GCCAGTGATATATAT[G/T]AAAATTTGTAATGAT | 64326 |
rs542602337 | in-del | -/ACTA | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176033046 | ATCAGCATGAGTTTC[-/ACTA]ACTGATTTCTAAAAT | 64326 |
rs542605627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176057102 | GAAAGACAAACTACC[C/T]CTGCGTTTCCAATAT | 64326 |
rs542607572 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176013937 | AAGATTACTCAGCCC[A/G]ATTTTATAATCATTG | 64326 |
rs542610413 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175982185 | GCATTGAATCCCACT[A/T]CAATTTCAAAAGAGT | 64326 |
rs542611862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175974070 | ATCTTATTCTGTAAC[C/T]ATTGGGGAAACACTA | 64326 |
rs542617311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176097838 | CATGCCACTGCACTC[C/T]AGCCTGGGCAACAGA | 64326 |
rs542629980 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176063380 | ATGTTTTATGTTTTG[A/C]CTGTCATTAACACAA | 64326 |
rs542632559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176012728 | TACATTTAGATACAC[A/G]AATACTTACCATTGT | 64326 |
rs542667627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176071585 | TGAATATATAACTGA[C/T]CTTAGGATCACAGAA | 64326 |
rs542673397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RFWD2 | GRCh38.p7 | 1:175967446 | AGCTGAGATTATGCC[A/G]CTGCACTCCAACCTG | 64326 |
rs542687229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176167599 | ACATTTGTTAATTAT[A/G]ATTCTACAGAGCCTT | 64326 |
rs542688703 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175980706 | TTTGCCTGAGGATAG[A/T]GTGTACTTTTTGGGG | 64326 |
rs542692250 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176200515 | GAAAAAATGTACCAC[C/G]CCAAACCACACAGAT | 64326 |
rs542693951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176007308 | CCTCCCGTAGCTCAG[A/G]GTAATTTGATCGTCT | 64326 |
rs542695106 | in-del | -/C | 0.00597247 | 0.0543191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176198640 | AGAAAAAAGAAAAAA[-/C]TTTTGCACTTTAAAA | 64326 |
rs542710564 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176193837 | ACAGAGTTTCTTTAG[C/G]GGCTGATAAAAATGT | 64326 |
rs542711212 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176095190 | TACATACAAAATAAT[A/G]AAACAAATTAACTAT | 64326 |
rs542718095 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176069706 | AGCAAATCTAAAAAA[C/G]TACCTGCCTCTGCAT | 64326 |
rs542722103 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176159759 | ACTTTATATGGTTGT[A/C]GATACTAACATACAT | 64326 |
rs542723457 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176198929 | ACTGAAAACACTGAG[C/T]ACTGGCAAGGATGTG | 64326 |
rs542726151 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176118325 | TTCAAAAATAAATCA[C/T]ATGAATCTGTCTACA | 64326 |
rs542741110 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176077127 | TAATTTATTCTATGA[A/T]TCCAGCATCATCCTG | 64326 |
rs542750080 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175981181 | TTTGCTGATTGAAAA[A/T]TTTTCAGGTTTATTT | 64326 |
rs542750507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176160832 | ATCTTTAAGTGTGCC[C/T]GTTATGAAGCAGTCC | 64326 |
rs542778151 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176070960 | GTGCAACCACTCCTG[C/G]TTCTGTCCAATTCTT | 64326 |
rs542787295 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176008288 | CTCAGATGGAAATGC[A/T]GAAATCACCCATCTT | 64326 |
rs542791345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176140635 | CTGTAAACATAACCC[C/T]GGGAAGGAGAACTTA | 64326 |
rs542793120 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176057448 | TGCCTGATTCTCCTG[A/C]CTCAGCCTGCCGAGT | 64326 |
rs542801934 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176130536 | AAATGGATGAAAGCT[G/T]AAAAGGTTAAAAAAT | 64326 |
rs542808033 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176041845 | GAAGCCAGGTGCAGT[C/G]GCTCACATCTGTAAT | 64326 |
rs542814445 | in-del | -/AA | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176061802 | ATTTCTACAGGATAG[-/AA]AAAAATTTTAAAAAT | 64326 |
rs542824333 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176090975 | TGTTTTTGTCTATAC[A/G]GCAAAAATATCTTAA | 64326 |
rs542825824 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175969629 | TATACAAGTTTACCC[A/G]TTCTTTGGGTCTTCA | 64326 |
rs542837949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175997597 | GGCGAAGGGAATGAA[C/T]AGACACTTCTCAAAA | 64326 |
rs542847306 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176196041 | TACTTCTGAATAATC[C/T]ATGTTTCAAATAAGA | 64326 |
rs542848317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176008267 | CTAGTGAGATGAACC[C/T]GGTACCTCAGATGGA | 64326 |
rs542851346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176131721 | TAGTATTATAAAAGA[C/T]AATATTTGTCTCAGA | 64326 |
rs542861184 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176084045 | CCATATCTATGCTGC[A/C]AGTGACTTAAAGATT | 64326 |
rs542864256 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176002511 | CCCTTCCCCTTCCCC[A/C]CCACCCCACAACAGT | 64326 |
rs542895189 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176098381 | TTATAAGAAGGTGTG[A/G]AAATGTAAATTTTTG | 64326 |
rs542920939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175982876 | CCAGAGGTGGGGGAT[A/G]GGAGTGGGAGGATGC | 64326 |
rs542921360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176131154 | GGGCTAGGCAATTAC[A/G]GAGGGTTATGCAAAG | 64326 |
rs542922924 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175974854 | TCTGACCAATATGGG[A/T]GGTCAAGGCTGCAAT | 64326 |
rs542938127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176002999 | GTGTTCCTATTTCTC[C/T]ACATCCTCTCCAGCA | 64326 |
rs542939757 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175996504 | CTAGAAAACCCCATC[A/G]TCTCAGCCCAAAATC | 64326 |
rs542955742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176201185 | AAATATTCTAAAATT[C/T]GAAAACAAAAACCAA | 64326 |
rs542955780 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176193741 | GCATTTATATGAAGT[C/G]TCTGGAATAGGTAAA | 64326 |
rs542959682 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176012551 | AAATAAATTTAGTAT[A/C]GCCTAAGTATACAGT | 64326 |
rs542964856 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175966873 | AGAGTGTTCCAAAGT[A/C]AACATACATGGCATT | 64326 |
rs542970993 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176121402 | CACAAGTAGTCAAAT[A/G]TATCACCCAAAATCT | 64326 |
rs542978195 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175982492 | ATTCACTTCATTTAA[-/T]TAAACAGTAAATATA | 64326 |
rs542980826 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176101635 | CTAGTCGGGCTTCTG[A/C]CCCCATCTCCCTGCA | 64326 |
rs542981237 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RFWD2 | GRCh38.p7 | 1:176192104 | CAATTTCTGGTATCC[A/G]TAACAGAAAAGCAAG | 64326 |
rs542981897 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176202227 | CAGGGTCTCACTTTG[C/T]CGTCCAGGCTGGAGT | 64326 |
rs542991494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176145799 | ACCTATGGATACTCA[A/G]GCAGCAAAACATTAA | 64326 |
rs543018820 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176086654 | GCTCATGGATAGGAA[G/T]AATCAATATTGTGAA | 64326 |
rs543019496 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176095109 | CTCAAACTAATTTCA[C/T]AAATTAACACTGCAT | 64326 |
rs543024077 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176127329 | ACTATAACTTTGTAC[G/T]CACTGACCAACTTCT | 64326 |
rs543024722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176189075 | AAAATATCCCTAACA[C/T]GTACAATGCACTTTA | 64326 |
rs543029333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176055251 | CCAGCCTGGCCAACA[C/T]GATGAAATCCAGCCT | 64326 |
rs543030443 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176148680 | TACCTAAGGCTTTAT[G/T]ATCTAAATTTTCCTA | 64326 |
rs543042699 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176185418 | TACTTTAAATACCAA[C/T]TGTAATCCTCTTCTG | 64326 |
rs543073310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176011876 | CACAAACCTACTGCA[C/T]TGACAATAAAATAAA | 64326 |
rs543088036 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176182382 | ACTTGTTCTTTTAGC[A/G]CTAGATGAGTACTTC | 64326 |
rs543109228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176020286 | ATTGCCCTCCAGCCT[A/G]GGCGACAAAGTGAGA | 64326 |
rs543114670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176058068 | GCCCGGCAGCCGCCC[C/T]GGCCGGGAGGGAGGT | 64326 |
rs543119244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176008806 | TGTAATTCCTACTGC[A/G]TGGAGCCACTGACAT | 64326 |
rs543134678 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176099653 | GCAACTGGATGCAAC[C/T]GGAGAAATGTTGTTT | 64326 |
rs543152630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176052208 | GTTAAAGCTACCTAC[A/G]GCATTCAGTACAGTA | 64326 |
rs543153878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175978064 | AGATTACAATAAAAG[C/T]TACTGTTAGGATAAT | 64326 |
rs543154461 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176059953 | AGTTGAAATTTGACT[C/T]GCAGGTATTAGTTTG | 64326 |
rs543158580 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176035284 | AAGAATCAAATGAAA[A/T]TTTTTGCAAAATGGA | 64326 |
rs543191344 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176004503 | TTGTCATAGATAGTT[A/C]TTATTATTTTGAAAT | 64326 |
rs543197863 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176179754 | AACAGAAAAAAAATT[G/T]TTTGTCAATATACAA | 64326 |
rs543198736 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175970834 | AGATAGAGGTACATG[A/C]AAATGCTGAATTTGA | 64326 |
rs543204931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176031596 | TACACTGTATTTATT[C/T]ACATATGGCCTCCTT | 64326 |
rs543221388 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175989144 | TAAAAAACTAGTATC[A/T]TCAGGATTTTACCCA | 64326 |
rs543229690 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176144422 | AATATAAAAATTTTA[A/G]GGCTATTTTAAAGAT | 64326 |
rs543232802 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175961270 | ACTTCTGTCCCTTTG[C/G]AGAACCCTGACTAAG | 64326 |
rs543234789 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175953115 | CAAATAATAAAAGGG[C/G]AGAATAGAAGTATAA | 64326 |
rs543242149 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992740 | GGTAAACAAAGCAGC[C/T]GGGAAGCTCGAACTG | 64326 |
rs543245525 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175958442 | TAAGGCACTGAATTA[G/T]CAAAAAGAAAGGTAA | 64326 |
rs543248548 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176122283 | GACATCATGTTTTAA[C/T]GCTGAAATATTAATG | 64326 |
rs543253158 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176033625 | AAATATATTTCTCCA[A/T]AAGAACCTTTAAAAT | 64326 |
rs543265232 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176000448 | TGGGAGCATAGAATT[C/G]TTTACACTAGTATCA | 64326 |
rs543272565 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176204293 | AGGATAAAATAAAAC[A/G]TGAAGCATAAGCATA | 64326 |
rs543274830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176138442 | TTTTCAAAAGCTTTC[A/G]ACTCATCTATCTACT | 64326 |
rs543297909 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176090250 | CTTTCCAGATCGAAT[A/C]AATGTAAACTTCCTA | 64326 |
rs543304662 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175984639 | CTGACAGCTTGCACC[A/G/T]TTCACCTGGAAAAGC | 64326 |
rs543316369 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176048887 | TGCTGTCAAAAGAAT[G/T]AAGGGCCGGGCGCGG | 64326 |
rs543316696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176146348 | CCTCCAAAGATCCCC[A/G]CCTCTTAGTATTCAA | 64326 |
rs543321784 | in-del | -/ATTA | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176204559 | TTAAATCAGATTCTC[-/ATTA]ATTAATTCTTCTGAA | 64326 |
rs543325809 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | RFWD2 | GRCh38.p7 | 1:176006444 | GTTTCTTCCTAGCCT[C/T]GATGGGCTTTACAAT | 64326 |
rs543327518 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176174404 | CCTGCAAGGTACCAT[A/G]CCACTCAATATTTCT | 64326 |
rs543345523 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:176087303 | AAGCAAAAGAAACTA[C/T]CATCAGAGTGAACAG | 64326 |
rs543362210 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176127718 | GGACAAAGAAGATGG[C/G]ACTTTTTTCATAGTG | 64326 |
rs543371005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176174970 | GGTTCTGACTAGTTA[C/T]TATTTCCGATCATTT | 64326 |
rs543382078 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176009322 | TATTCTAATATTTCA[A/C]AATTCAAAAACATTT | 64326 |
rs543422802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175965012 | AGATGATTTCATGTC[A/G]CTGAAAATAAAAGAC | 64326 |
rs543426364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176142787 | GCCACAGGCCTAAGA[A/G]AAAAATATAATGAAA | 64326 |
rs543431860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176168867 | TAGTGCTTACAGCAG[A/G]AAAGAAAGAAAATCA | 64326 |
rs543432271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175947571 | GACGGGGATTCTCCA[C/T]GTTGGTCAGGCTGGT | 64326 |
rs543442023 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176077859 | TCCATATACTAATAA[C/T]ATTCTAGCTGAGAAA | 64326 |
rs543459221 | snp | A/C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176149185 | GCACCCATTTAAGTT[A/C/T]GTCTATTATTTCTAT | 64326 |
rs543461044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175978945 | GACCGTATCTTACTT[C/T]TTTGGATTTGTTTCT | 64326 |
rs543461848 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176156585 | ACAATGACAGAACTA[A/C]AGTACAAGCATGAAG | 64326 |
rs543466153 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176030148 | AGTAGAGATGGAGTA[A/C]GATTTTTAAATAGCA | 64326 |
rs543468604 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176078513 | TCAATCAAAACTTAA[C/G]TCTAAGACCTCAAAC | 64326 |
rs543471581 | in-del | -/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176112271 | TCCTCCAGATTCAAG[-/T]TTTTTTTTTTAAATC | 64326 |
rs543483449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176051088 | AGGTAGCCTCACCGG[C/T]TTTATAATTAGTAGA | 64326 |
rs543487296 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176042853 | GGCTAACATGTTGAA[A/G]CCCCATCTCTACCAA | 64326 |
rs543488284 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | RFWD2 | GRCh38.p7 | 1:175993887 | CAGATTCAGGAAATA[C/T]AGAGAACGCCACAAA | 64326 |
rs543498906 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176148833 | ATGATTTTTTAAGTG[G/T]CAAGTTGTAAAGAGA | 64326 |
rs543516890 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176025460 | TTGTCTACATTTAGC[-/A]AAAAAAAAAAAAACC | 64326 |
rs543540546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175954874 | ACAAAAAGAATAATG[C/T]ATCATGTCTAAATGG | 64326 |
rs543547665 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176181180 | TGCTATATTGTCTCC[A/C]AATTGTTACTAGGAA | 64326 |
rs543553155 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176059046 | CCAGCACTGCCCTCT[A/T]ACTTCAAGGGACCTT | 64326 |
rs543559901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176133218 | TATGTACACACATAC[A/G]TATATACGTACGTAT | 64326 |
rs543564024 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175958546 | AGCATTTCCACCCTA[C/T]ATTTCTCCTCCTTTT | 64326 |
rs543573056 | in-del | -/AACT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176095098 | AATACTTTTTTCTCA[-/AACT]AATTTCATAAATTAA | 64326 |
rs543580507 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176086283 | CAGGCTGGAGTGCAG[C/T]GGCACCATCTCAGCT | 64326 |
rs543612996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176113453 | ATTAATCCCTTGTCG[A/G]ATAGATAATCTGCCA | 64326 |
rs543617179 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176013015 | ATCCACGGATGTTCA[C/T]GTTTCTTTTACAAAG | 64326 |
rs543618631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176032262 | AACTACCATAAAACT[C/T]AGGGGCAATGTGTAT | 64326 |
rs543621875 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176197117 | GTAAAATACAGTCAT[A/G]TTGGTGGACCCCAAT | 64326 |
rs543635460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175949398 | GTTCTGGATGTCCTT[C/T]AGGAATATAATAACT | 64326 |
rs543647583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175950000 | TATAAATAAGATAAT[C/T]TAGTTGGATTACCAC | 64326 |
rs543652721 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175978824 | GAAGCTTCTATGTTG[C/T]CTTCTCCGCACTCAT | 64326 |
rs543658705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176174281 | CATCTTTAGTGATCC[C/T]AGATTCCACAGGGCA | 64326 |
rs543660543 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176072378 | GCAAGAAATAAGACA[A/G]GTAAGGCCCCTGCCT | 64326 |
rs543681356 | snp | A/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176208461 | TGTCTCAAAAAAAAA[A/T]ATTTTTTTCATTTGC | 64326 |
rs543699463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176182987 | GATAAAGGTGGACAT[C/T]TGTATTTTATATTAC | 64326 |
rs543705039 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176107842 | CTATAGTATTCCTGA[C/T]GAAAATAGATAATCT | 64326 |
rs543716271 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176045202 | ATAGGTCTGCTAAAG[A/T]CCAAGCACTTAGGAT | 64326 |
rs543729595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175957844 | AAAATGGATTACTAA[C/T]AAGAAGGAACTACAG | 64326 |
rs543731395 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176087738 | AATACCATTTGACTC[A/C]GCCACCCCATTACGG | 64326 |
rs543759464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175989813 | AAACCATTATTTAGA[C/T]ATATTTTGCATATAA | 64326 |
rs543788653 | snp | C/T | | | synonymous-codon | RFWD2 | GRCh38.p7 | 1:175986958 | CCCATCTGGTAGTGC[C/T]CTCCAGCACACAGCA | 64326 |
rs543813019 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176037675 | TGACTATAATTCATA[A/C]TATTAATAAAGAGAA | 64326 |
rs543814630 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176172149 | AAAATCCTCAGGCTC[A/C]CATGATCCTCTCACC | 64326 |
rs543824245 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176172824 | TCTGAGCCAACAGGA[C/G]ACAGTCTCTACACAC | 64326 |
rs543826029 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176166145 | ATTTATTTATTTATT[C/G]AGACAGGGTGTGACT | 64326 |
rs543837365 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176126014 | TTTATTCTTTTTCAC[A/T]TCGTTCACTGCTGGC | 64326 |
rs543848603 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176004582 | GTTGCATTTTGTTGA[A/C]GGCTTTTTCTGCATC | 64326 |
rs543859920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176131050 | ATCCAGGAGAAGTTT[C/T]TAGGCAAAAGGAACA | 64326 |
rs543875419 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176119919 | TATATATGTGGCCCA[A/C]GATAACAACACTGGG | 64326 |
rs543878895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176035159 | TTAAATGAAACAGAT[C/T]TTAAAGCAACTATTG | 64326 |
rs543902694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176124487 | CACGAGTTCAATTGA[C/T]TTTTAGATCCCACAA | 64326 |
rs543918756 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | RFWD2 | GRCh38.p7 | 1:175965650 | CTGGACTGCAGTGGT[A/G]CAGTCTCGGCTCACT | 64326 |
rs543928055 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176093053 | ATCTCTGAAAAAACA[A/T]ATCTCAGAAATCTTA | 64326 |
rs543946855 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175999262 | CAACAGCCCAAGTAC[A/C]CTTCTCAGACTCTGG | 64326 |
rs543986092 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175969754 | TTTCTCCCTTACAGC[A/G]TGTAACCAAAGAGTA | 64326 |
rs544008950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175959601 | ATAAGAGAGTTTAGC[A/G]AGATGGTTGGATTAA | 64326 |
rs544013252 | snp | A/C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176175001 | ATCATTTATACTTAA[A/C/G]GATTCCCTATTCATG | 64326 |
rs544018319 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176023775 | AGTAAACACATTGAA[A/T]TAGGAATTTAAAATC | 64326 |
rs544036164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176016684 | TATTTTGTATGGAAT[C/T]TGTAATACACTTTTA | 64326 |
rs544047921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176079200 | CTGGTATGTTCACTG[C/T]AGAGCTATTCACAGT | 64326 |
rs544053298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176069186 | TGAGACCTCATCTCA[A/G]GAGAAAAAAAAAAGA | 64326 |
rs544096363 | in-del | -/TCT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176069728 | CCTCTGCATCCACTC[-/TCT]TCTTGTTTCCTTATA | 64326 |
rs544122071 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176199586 | TATAATGGGATAATA[A/C]TAAGCAATTAAAAGA | 64326 |
rs544125564 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176126488 | TTTGAGATGGAGTCT[C/T]GCTCTGTCACCAGGC | 64326 |
rs544137778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176070082 | TTAGATATCCCCCAC[A/G]AACCCTGTTGCTACT | 64326 |
rs544160262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176115613 | AATTAGCTGGGCGTG[A/G]TGGCGCGTGCCTGTA | 64326 |
rs544192809 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176018180 | TTGTGAATAATCTCT[C/T]CAACCCTTACCAATC | 64326 |
rs544194279 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176172193 | AAGCTAGGACAACAG[-/C]TGCATACCAACACGC | 64326 |
rs544204757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176018969 | TCAGGAGTTCAAGAC[A/G]AGCCTGGCCAACGTG | 64326 |
rs544204936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176010063 | GCAAAGAAGCTGAAA[A/G]AACAGCACAATGAAT | 64326 |
rs544207487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176027431 | AGTAATGATGGCATA[C/T]TGTATACTTCTAATT | 64326 |
rs544207834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176075823 | GCCTGGCCAACATAA[C/T]GAAACCTAGTCTCTA | 64326 |
rs544224617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176123829 | TGTCAGATTTAAGAA[C/T]TTATTCAAAAACATG | 64326 |
rs544255040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176060175 | TAAAACAACTACTTT[A/G]AAAAAATTTACTTTC | 64326 |
rs544258000 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992456 | GGCATTGCCTCACTC[A/G]GGAAGCGCAAGGGGT | 64326 |
rs544261586 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176137336 | ATTCTGGAACATATT[A/G]TTCTTTCAGATTTCA | 64326 |
rs544269216 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176025753 | AAATTAGCCAGGTGT[A/G]GTGGTGCACGCCTGT | 64326 |
rs544271628 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176177457 | CTTCTCTTAAAAAAT[C/T]ATATATGTGTACATT | 64326 |
rs544290416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176034678 | GTTCTGTGCATTCAC[C/T]GGCACAGTCACTTCT | 64326 |
rs544298297 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176130228 | CTGAGCTAAAAAGTT[A/T]AAAAATGTCTAAAAT | 64326 |
rs544323781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176122887 | ACAGGTCTGAGTCTA[C/T]TGCTTTATCACTTTT | 64326 |
rs544325626 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176115229 | CAAGGTGGGTAGATC[A/T]CCTGAGATCAGGAGT | 64326 |
rs544337869 | in-del | -/A | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:175966229 | TTCCCTGCATTCTAT[-/A]AAAAAATCCAAGGGG | 64326 |
rs544339701 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175990797 | CCATTCTACCATTTT[C/T]CTTGACTACTACTTA | 64326 |
rs544362878 | in-del | -/AG | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:176123469 | TAATTAAAGGGGAAA[-/AG]AGTTTCCTATGTGAC | 64326 |
rs544375313 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176123875 | TATCACCAATTACTT[A/C]ATCTTCCCATATTTT | 64326 |
rs544376599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176199099 | GAGGCGTGGGGACCA[C/T]GAGGTCCAGGGATCG | 64326 |
rs544378944 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175993876 | AGGCCAACTTTCAGA[G/T]TCAGGAAATATAGAG | 64326 |
rs544378999 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176021624 | TTGCAAATAAATAAA[C/T]TGATTTATCTCAAAA | 64326 |
rs544412461 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176020438 | CACACCAGCACTTTG[C/G]GAGGCCAAGGCAGGT | 64326 |
rs544422519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176012928 | ATCCTTGAGCAACAC[A/G]TGATTGCATTATGTA | 64326 |
rs544426560 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176040169 | AAATAAATATATCTA[C/T]TGTAACATGGTACTC | 64326 |
rs544428432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176047817 | CGGTGGCTCATGCCT[A/G]CAATCCCAGCACTCT | 64326 |
rs544444738 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176018190 | TCTCTCCAACCCTTA[C/T]CAATCCACAATAGAT | 64326 |
rs544458988 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176151203 | TCCCATTTTCGGATA[A/C]GGAAGCGTGTAAGAA | 64326 |
rs544468732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176111531 | ATCTCTTGACCTTGC[A/G]ATCCACCTGCCTTGG | 64326 |
rs544501859 | in-del | -/T | 0.000370081 | 0.0135979 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176184718 | AAGAAAAATAATTGA[-/T]TTTTTTTTAAAAGTA | 64326 |
rs544505347 | snp | C/T | | | intron-variant, utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175967806 | TCATATCTAAAGTAT[C/T]GACCTTCACTGGTAA | 64326 |
rs544507238 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175980825 | TAAGTACGTATGTTA[C/T]GGTTCAGAGCTGACA | 64326 |
rs544507970 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176126170 | CATCTGTAAACAGGG[A/G]TAATTTGACTTCTTC | 64326 |
rs544516124 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992676 | GATCAAACTGCAAGG[C/T]GGCAGCGAGGCTGGG | 64326 |
rs544520397 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175994901 | CAAGCAGACTTAATG[C/G]ACATCTACAGAACTC | 64326 |
rs544521082 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176006811 | TCAACTTTGGTGAAT[C/G]TGACAATTATGTGTC | 64326 |
rs544521157 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176051176 | AATTCAGGAGGCAAT[A/G]ATTATTGGGGCTCAT | 64326 |
rs544540502 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176117199 | CTAGAGTCCCTCCCA[C/G]CTTCAAAATATTATA | 64326 |
rs544544782 | snp | A/C/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176140624 | CTAAATTCACTCTGT[A/C/T]AACATAACCCCGGGA | 64326 |
rs544547190 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176144628 | CCAGACTTTAAAGAA[C/G]AACAGCAACTTAATT | 64326 |
rs544555410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176112908 | TTTCATTCTTTTTTA[C/T]GGCTGAATAATATTC | 64326 |
rs544562417 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176076161 | CACCCAACAACCACA[A/G]AATATACAAACTCCT | 64326 |
rs544576978 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176204350 | AGAAATTATCATTAT[A/T]TGAACTTGGGCTTCG | 64326 |
rs544591333 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175979256 | ATTGTTTTTGAAAGA[C/G]CCCCAGGGTTTTCTG | 64326 |
rs544595535 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176067886 | TGGGGTCAGAGCCCA[A/C]GCTCCCACGATCTGC | 64326 |
rs544621372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176151853 | CTATAAATGAGTAAT[C/T]TGGTCCTTACAGGTT | 64326 |
rs544632412 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176108522 | GCCAAATTATCTTCC[C/T]GGACGACTATCAACT | 64326 |
rs544642256 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176109349 | TAAATTTCCTTCAAA[G/T]AGTTTCCCATTTGTC | 64326 |
rs544642891 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176101405 | CCAGGACTCCTTTGG[-/A]AAAAAAAAAGGCTTT | 64326 |
rs544647524 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176201485 | CAGTAACAGTTCTTA[C/G]ATGGAACATATCCAC | 64326 |
rs544651232 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176015696 | TGACTGCAGGGAAAG[C/G]AACAAAGAGAAGAGA | 64326 |
rs544663296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176197293 | GGTGACACATGCCTG[C/T]AGAGCCAGCTACTAG | 64326 |
rs544668490 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175955068 | GCCTGGGCAATATGG[C/T]GAAACCCTCTCTATC | 64326 |
rs544692723 | in-del | -/CC | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176002189 | TACCTCTTTCTCTCT[-/CC]CCTCATCTTTTGGAA | 64326 |
rs544699133 | snp | A/G/T | 0.00597247 | 0.0543191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176047803 | TTTCAGGCTGGGTTC[A/G/T]GTGGCTCATGCCTGC | 64326 |
rs544701923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176171483 | TCCATATCAGCAATA[A/G]GCGATTTTGCCTTCT | 64326 |
rs544727642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176106860 | GGTGAATCCATTGAG[C/T]GGTTACATGACTAGC | 64326 |
rs544733791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176071675 | ACTGCCTCCTGAGGA[A/G]GGTTATTCTACCTCA | 64326 |
rs544745667 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176139818 | GGGTGGGGGAAGGAA[A/G]AAAGGGTTGAAGAAC | 64326 |
rs544755257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176067488 | GGCACCAGCAGACAC[C/T]GGCAGGCCATCAACC | 64326 |
rs544773872 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175988939 | TTTAAAACCAAAAAT[A/T]ATTCTACTACTATAC | 64326 |
rs544780712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176096546 | TGGCCAGACTACCAT[C/T]GGTCTGAGCCAGGGG | 64326 |
rs544781343 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175965345 | GATATAAGATATAGG[A/G]ATTCTTAAATTTTTC | 64326 |
rs544785266 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176141879 | GGGACTACAGGCACA[C/G/T]GCCCCTATGCTCCAC | 64326 |
rs544786728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176191469 | TCAAAACTTGAAATT[C/T]CTCTAGCTTCCTCTT | 64326 |
rs544789610 | in-del | -/TTTT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176008832 | GACATCTTTAATGAG[-/TTTT]TTATTTATTTTTGTT | 64326 |
rs544811093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175959284 | AAGAACTCTCAGCAC[A/G]TTGAGAACTGAAGGA | 64326 |
rs544827139 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176037140 | AGGCGCAGTGGCTCA[A/C]GCCTGTAATCCCAGC | 64326 |
rs544830351 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176180689 | TATAAATATCTTTTT[A/T]TATCTATGTAAACAA | 64326 |
rs544831627 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176001744 | GTATCCCTTTATTTC[A/G]GCCTGCAGAACTCTC | 64326 |
rs544836009 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175973531 | ATATTACTGTTTACA[A/G]AGTGGTGGAAAGAAG | 64326 |
rs544854001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176060815 | TCAGTTAACACAGCA[A/G]ACTTAAAAAATCAGA | 64326 |
rs544857123 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176004605 | TCTGCATCTATTGAG[A/G]TAATCATGTGGTTTT | 64326 |
rs544866644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176103187 | GAGTTTCCTGAGTGA[C/T]ATCAGCATCTTTTGT | 64326 |
rs544870189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176008314 | ATCTTCTGCGTTGCT[C/T]ATGCTGGGAGCTGTA | 64326 |
rs544874898 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176158457 | AAAGAATAAAGGACA[C/T]CAGAAATGGTAAATA | 64326 |
rs544895821 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175955965 | CCAATTAAAATCATA[A/C]AAACTTTTCTAGTAG | 64326 |
rs544906839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175979963 | AAACACGCTGTGTAA[C/T]GCTAGGGGTAATTAA | 64326 |
rs544919406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175999360 | GAGAATCCGTGACGT[C/T]TGTCTTTCTATGCCA | 64326 |
rs544938776 | in-del | -/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:175986327 | CTAGCCTAAGAATTA[-/T]TTTTTTCATATAACT | 64326 |
rs544940435 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176106433 | CACTGGCCACAAGAT[A/C]AGAAATTATAGTTTA | 64326 |
rs544944983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176141332 | AAGGTGACACCCTGT[C/T]TCTACTAAAAATATA | 64326 |
rs544950290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176100139 | TCACGCCTGTAATCC[C/T]AGCACTTTGGGAGGC | 64326 |
rs544959327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175968181 | GGCAAGAGAAGAATA[A/G]TATTTCCACATTCAT | 64326 |
rs544973418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176022882 | GCTTCTAGACATGAA[C/T]TAGATTCCATCAATC | 64326 |
rs544977109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176051117 | GAAGAGATTACAGAC[A/G]ATATATGCAAATGTC | 64326 |
rs544984697 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176201464 | TAAGGCTACAGTTAC[C/T]TTAATCAGTAACAGT | 64326 |
rs544992815 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176038167 | TTTTTAAAAATACCA[C/T]TTTCATTAGCACCAA | 64326 |
rs544994870 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175975512 | CCTCCTGGGTTCAAG[A/C]GATTCTCATGTCTCA | 64326 |
rs545057930 | in-del | -/ATG | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176066757 | TTCCTTCACCAAAAA[-/ATG]ATAACTAGAACAGCT | 64326 |
rs545063655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176049422 | TAAGGTATCAAGAAC[C/T]TGTAGAGTATGTTTT | 64326 |
rs545069702 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176194568 | ACTCGAACCCAAGAG[A/G]AGGAAGTTGCAGTGA | 64326 |
rs545070448 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176199907 | TATGACCAGTGACTT[A/T]TTTTATGCAAATTAT | 64326 |
rs545080732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175974164 | CTAAACTAAATGGCA[A/G]GAGCTTGAACTAAAG | 64326 |
rs545092464 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176200671 | TTGTGAAAAATGAAA[C/G]GACAACTAACATATT | 64326 |
rs545094840 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175961345 | TCAATCATCACAGTC[A/G]TTTCATTATACAGTA | 64326 |
rs545107671 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176192954 | AATATAGTACCAATT[A/C]AACTAGTCTTCTATT | 64326 |
rs545110255 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176168776 | AAGGGAGAAACAGAA[A/G]AGAATGAGAGAAAAT | 64326 |
rs545115003 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:176003139 | TTCATGTGTTTTTTG[A/G]CTGCATAAATGTCTT | 64326 |
rs545126959 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176153392 | GGTAGTTCCCAAGTC[A/T]TTGTACTGACAGAAA | 64326 |
rs545127691 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176173498 | AAACAAAAATAGCCA[A/G]GTATGGTGGCGCATG | 64326 |
rs545129426 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176049668 | AACATTTGCTCCCTA[-/T]CTCTGACATATTTAA | 64326 |
rs545131763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176072251 | GCAAATATGTGGACA[C/T]ATATGGACAAATGCT | 64326 |
rs545136838 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176040561 | GCCATCCTCCTGCCT[C/T]AGCCTCCAAAATTGC | 64326 |
rs545142612 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175974634 | TAATTTCAGTGAAGA[C/G]ATTATGAGAAAGAAT | 64326 |
rs545171043 | in-del | -/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176016149 | TAGAAATGTCTGGAG[-/T]TTTTTTTTAGCTAAG | 64326 |
rs545174359 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175990503 | GTCTGTTATGTCAGA[C/T]TGACAATGTTATTCA | 64326 |
rs545178656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176051715 | GTGAGACAAGATGTG[A/G]AAGAGATCACAGTGA | 64326 |
rs545193023 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176077109 | CAAGGAGGGGCTTCT[C/T]CCTAATTTATTCTAT | 64326 |
rs545211230 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176044208 | CCTGGATCCAGTTGT[A/G]CCAAATCATATAAGC | 64326 |
rs545224165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176119278 | TTTGTATAACACTAA[C/T]AAAATTGTGTAGTTG | 64326 |
rs545224882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176093969 | CGGAGGTTGTAGTAA[A/G]CTGAGATTGTGCCAC | 64326 |
rs545226636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176086366 | AAGTAGCTGGGACTA[C/T]AGCCGCCCGCCACCA | 64326 |
rs545230199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175993472 | GGAAACTTAAACCAA[A/G]GGCAAAGAAGTTGAA | 64326 |
rs545231653 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176004987 | CATCTGGTCCTGGAC[C/T]CTTTTTGGTTGGTAA | 64326 |
rs545243191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175963778 | CAAGTTAGAAGTAAC[A/G]TCTTCCCTCTAGGGT | 64326 |
rs545254809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175997655 | ATGAAAAAATGCTCA[C/T]CATCACTGGCTATCA | 64326 |
rs545261852 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176125481 | CATTTATTTAAGAGA[A/T]TATCTTTTCCCCAAT | 64326 |
rs545270447 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | RFWD2 | GRCh38.p7 | 1:175976429 | ATTACAGGTGTGCAA[C/G]ACCATGCCTGCCTAA | 64326 |
rs545280597 | snp | A/G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176204821 | TCCCAGCTACTACTC[A/G/T]GGAGGCTGAGGCTGG | 64326 |
rs545288156 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176057523 | TATTTTTTTGGTGGA[C/G]ACGGGGTTTCGCTGT | 64326 |
rs545307117 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176075965 | CCAAGATCATGCCAT[C/T]GCACTCCAGCCTGGG | 64326 |
rs545313555 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176121526 | CGTTTTTTATTTTTA[C/T]GTTTTTAGAGGTACG | 64326 |
rs545314870 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175993173 | CTACAACAGACCTGC[A/T]GCTGAGGGTCCTGTC | 64326 |
rs545315100 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176151794 | GAAAACACATTGGTC[A/G]TAACTATGTAAATAA | 64326 |
rs545323459 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176057921 | CCGCCCATCCTCTGA[C/G]ATGTGGGGAGCACCT | 64326 |
rs545331329 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176187623 | ATCCTAGCTATGCCA[G/T]CTACAGCTTTGTGAC | 64326 |
rs545338476 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176168079 | TTTTTTTTTTTTGAA[A/T]CAGAGTCTCGCCCTG | 64326 |
rs545352916 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176098090 | CAGATATTAGGTTTG[C/T]TAAATGTTTTAAGGT | 64326 |
rs545354678 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176194227 | CAAGAAAGGAAGAAA[A/C]AAAGAGAAAAGAAAT | 64326 |
rs545366208 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175969728 | ATCAAGCCAACAGGT[A/G]AGAAAAATCTTTTCT | 64326 |
rs545376474 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176131153 | GGGGCTAGGCAATTA[C/T]GGAGGGTTATGCAAA | 64326 |
rs545377231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176180478 | ACAAAGAGGTAAAAG[A/G]GACACATATCTCGGG | 64326 |
rs545401197 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176163319 | GTAGTAAGGTATTAA[A/G]CTCATTTGCCTCCAT | 64326 |
rs545410091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175953796 | TCCTATATACATATA[C/T]ATCTAAAACAAAGCC | 64326 |
rs545411809 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176155970 | CAGATGGATGCGAGA[A/C]AAAATGAAGAGCATC | 64326 |
rs545421408 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176179838 | TATTCCACATCAATA[C/G]GCTTACTACACTATC | 64326 |
rs545421831 | in-del | -/TCTTTTC | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176041358 | TCTTTTTTTCTTTTT[-/TCTTTTC]TTTTTTTGAGACAGA | 64326 |
rs545435918 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176133645 | GGCATTCAATAAATA[C/G]AGCAATTAAGTAAAT | 64326 |
rs545443656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176041969 | ATACAAAAATTAGCC[A/G]GACATGGTGGCACGT | 64326 |
rs545448030 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176123832 | CAGATTTAAGAATTT[A/G]TTCAAAAACATGTCA | 64326 |
rs545468138 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175994757 | AAGCAAGTCCTGAGT[C/G]ACCTACAAAGAGACT | 64326 |
rs545471291 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:175982066 | AGAGAACTCTTGTAA[C/T]GTTGGTGGGAATGTA | 64326 |
rs545472429 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176145863 | GAATATTGGTTACCT[A/T]ATGGGCAAGGAAGAT | 64326 |
rs545472486 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176141722 | TTAACCCTTTCATAG[A/C]ACTTTTTCTTTTCTT | 64326 |
rs545479195 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175971849 | TTATTATCTAATGTC[G/T]CCCTTGGATTTAGTC | 64326 |
rs545485502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176048941 | ACTTTGGGAGGCCGA[A/G]GCGGGTGGATCATGA | 64326 |
rs545488172 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176129769 | AAAGAATAAAGCAAT[C/T]ATGAGATAACTATTT | 64326 |
rs545503997 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176046801 | GAATTACTGAAGCAA[C/T]TGGGTGATGACAAGG | 64326 |
rs545543633 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175965162 | CTGAAAACTAAAATA[G/T]CTTCTCTCCTCATGT | 64326 |
rs545552358 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176117317 | ATATACTAGTTTCCT[C/T]TGCTCTGGTCAAACA | 64326 |
rs545560262 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176146534 | TTGAGAGGCAGCCAG[A/C]TGCCATGTAGTGAGC | 64326 |
rs545563329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175978976 | TCCTGAGGTAGGTGA[A/G]GGATCAGCAAAATCT | 64326 |
rs545597393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175945866 | TGCTCAGCTAAGGCT[C/T]GACTAATATATGTGC | 64326 |
rs545610967 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176086339 | CTCGACATTCTCCTG[C/G]CTCAGCCTCCCAAGT | 64326 |
rs545614295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175988477 | AAACTCATCACTACT[A/G]ATTAGAGGCAATGCA | 64326 |
rs545617568 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176036515 | AAAAAAACAAAAAAA[A/C]AAAAAAAAAAAGCAT | 64326 |
rs545619349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176115616 | TAGCTGGGCGTGGTG[A/G]CGCGTGCCTGTAGTC | 64326 |
rs545626400 | snp | A/G | 0.00755907 | 0.0610114 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207390 | CTCCCTGGCGAAGGG[A/G]GTCTGTCTGTCCCAA | 64326 |
rs545635895 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175946516 | TGGAAAAAACAGGTA[C/T]TCTCAGAAACACGTA | 64326 |
rs545636582 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | RFWD2 | GRCh38.p7 | 1:176003855 | TTTTGGTTCCATATG[A/T]ACTTGAAAGTAGTTT | 64326 |
rs545647637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176051457 | ATGCTGCCAGTTGTA[C/T]AAAAGTACAGCACAC | 64326 |
rs545650736 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176131838 | AATCCTTGAGTGATA[C/G/T]TCACATCACTTGTTC | 64326 |
rs545656081 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176133398 | TTAGGTCTCTTTATG[-/T]GCTCTATTATTTTCT | 64326 |
rs545659228 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176064816 | TTTGTAGAGATGGAG[-/T]TTTCACCATGTTGCC | 64326 |
rs545682375 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176088469 | CAAGATGAATGTTCC[A/G]TATGTTCATCTCGGT | 64326 |
rs545683087 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176140411 | CAGGCAAGAAATATT[A/C]AAAAGAAAAAAGTTT | 64326 |
rs545683459 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176173689 | TTCATTAGATACATA[C/T]ATTTGAGAATATCTA | 64326 |
rs545697073 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176142500 | AATGAGACAGTAATA[-/G]GTATAACAAGGAAAG | 64326 |
rs545716203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175962341 | ATTATTACCAAAGAT[A/G]AGATGGTACTGAGAA | 64326 |
rs545730555 | snp | A/G | | | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207605 | GGGTATCCGCCCCAA[A/G]CGGAGAATATCGGCG | 64326 |
rs545742864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176046004 | TCACAAGAAAAAAGC[A/G]ACCAATATCTGTAAG | 64326 |
rs545747557 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176128787 | CTGCATTAAAAAAAA[A/T]TTCCAAATAAAATAA | 64326 |
rs545752805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176035994 | AAGGAAATTTAAATA[C/T]ACTTTAAACAATCCA | 64326 |
rs545754082 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176169874 | CTCACAGTAGAATTT[C/G]TTTCAAAGTTAGTCA | 64326 |
rs545755855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176170998 | GGCTTGGTGGTGGGC[A/G]CCTGTAATCCCAGCT | 64326 |
rs545775150 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176117159 | GTAAAAATGAGGTGA[C/T]GTAGGCTAGCTATTT | 64326 |
rs545782938 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176083009 | ACCTAACAGGCAATA[C/T]CATAACGGTATTGAG | 64326 |
rs545788861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175948517 | AGAACAAAGAAAACT[C/T]TTGGCTTGTATGTTA | 64326 |
rs545791304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176135571 | TTTATATATATTCTT[C/T]ACAAATATTAAGATT | 64326 |
rs545793186 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176144420 | AAAATATAAAAATTT[G/T]AAGGCTATTTTAAAG | 64326 |
rs545806405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175958550 | TTTCCACCCTACATT[C/T]CTCCTCCTTTTATTA | 64326 |
rs545814777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175959138 | TGGGCTTATTCCAGC[A/G]AATGTAAAGTTGGTT | 64326 |
rs545816176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176001044 | TCAACAATTTTAGAA[C/T]TACTATTTTAGTCAA | 64326 |
rs545817770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176163426 | AAGTCTCGCTATGTT[A/G]CCCAAGCTAGTCTCA | 64326 |
rs545832903 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175993803 | GGGGAGAATGGAACC[A/T]AGTTGGAAAACACTC | 64326 |
rs545835617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176039193 | GCTGAAAAATTCCCA[A/G]ATAATTCTAAGTAAC | 64326 |
rs545860734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176133931 | ATACACAGACCAAGT[C/T]ATTCTCAAATGTTTC | 64326 |
rs545864578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176142918 | AAAAAATAATCTGCA[C/T]AATAATATGCATATC | 64326 |
rs545865911 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176120648 | ATTCTGCTATGCAAG[C/G/T]AGATGTCCGTATAAC | 64326 |
rs545886144 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176053456 | ACTGTCATTTTCTTA[A/C]AAATTATTCCTTGCC | 64326 |
rs545886277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175949084 | AGGGGAAGTGCTTGA[A/G]CCTGGGAGGCACAGG | 64326 |
rs545888723 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176023977 | ATAAGAAAACTACAG[A/G]CCGGGCATGGTAGCT | 64326 |
rs545894546 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176072870 | AGTATAAAAAATATT[C/T]ATTATTTTGACCTCC | 64326 |
rs545896353 | snp | C/G | | | intron-variant, utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175971570 | TGTTTCCAAGAGTCA[C/G]CAGCACAGACCTATT | 64326 |
rs545928245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176037801 | TTTAAATTGACACAG[A/G]TGCCTACTAAAAGCC | 64326 |
rs545944982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176171536 | GTAGCACTTTTAATT[C/T]CGTTCAAGAACTTTT | 64326 |
rs545947429 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176078715 | AAACAGACAGCCTAG[A/G]GAATGGGTGAAAGTA | 64326 |
rs545967106 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176122959 | AAAAATAAGCTCAAA[C/G]GAATAAGACCAACAA | 64326 |
rs545982595 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176126731 | TGCTGGGGTTACAGG[A/C]ATGAGCCACTGCACC | 64326 |
rs545995558 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176075120 | TATGCCTAGTCTGGC[C/G]TAGCCTGCACTACGT | 64326 |
rs546004450 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176111498 | CGGGGTTTCACCGTG[C/T]TGGCCAGGATGGTTT | 64326 |
rs546009927 | in-del | -/AGTAAACC | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176104529 | ACTAATAAGTATATT[-/AGTAAACC]AGTAAACATATGAAA | 64326 |
rs546019727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176032862 | CATGATGGATGCTGA[C/T]CAACATAAGTCTTTA | 64326 |
rs546044376 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176165469 | GGAGGCCAAGGTGGG[A/T]GGATCACCTGAGGTC | 64326 |
rs546073891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176164171 | TTGGCACTTGCTGAG[A/G]GAGAAATCCTCATTC | 64326 |
rs546075684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176177527 | GTATTTGTTTCTGGG[C/T]CATATAATTATGGGA | 64326 |
rs546095506 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176163703 | CAATCCTAAACAATC[A/G]CCTTTTAAGAAAAAT | 64326 |
rs546126169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176017925 | ACTGAAAGAAAGCTA[C/T]TCTTTGACAAAAGAG | 64326 |
rs546153861 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176039829 | GGACAGTTTTTTCAA[A/C]AAGTGATGATGGAAA | 64326 |
rs546167577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176127472 | TCTGTGCCTGTCTTA[C/T]TTCACTTAACATAAT | 64326 |
rs546205989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176156647 | TAAGATGCTGTGGCT[C/T]TATCAGTATCAGACA | 64326 |
rs546206368 | snp | A/G | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176121381 | CACATACCCTTTAAC[A/G]TTTGACACAAGTAGT | 64326 |
rs546209583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176061870 | TGTTCCTTGAAAGAC[A/G]CTATTAAGAAAATAC | 64326 |
rs546228265 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175976750 | ATTCTTGGCTGCTAC[A/G]AAAAAGAATTACATA | 64326 |
rs546251745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175990510 | ATGTCAGATTGACAA[C/T]GTTATTCAAGTCTTC | 64326 |
rs546251846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175994525 | CAGAGACACACATAG[A/G]CTCAAAATAAAAGGA | 64326 |
rs546260008 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176054613 | TGTCATTCCGAACGA[C/T]GTGCTCCTAGATGTA | 64326 |
rs546267436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176166246 | ATCCTCCCATCTCAG[C/T]CTTCCCAGTAGCTAG | 64326 |
rs546267456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176158955 | CTAAGGTTCTTGTAA[C/T]ACAGATGAAGTAGTA | 64326 |
rs546276379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175993905 | AGAACGCCACAAAGA[C/T]ACTCCTCGAGAAGAG | 64326 |
rs546276869 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176019820 | GAGCCAAGACCACAC[A/C]ACTGCATTGCAGCCT | 64326 |
rs546283915 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176192320 | TAGTTATAAGTTAGG[C/T]ACAGGTGAAACAATT | 64326 |
rs546287267 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176119808 | CTGACGGTTTACTAT[C/G]CACTAACCTAAATAA | 64326 |
rs546318276 | snp | A/G | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176185051 | CACATGTACTCAAAA[A/G]CGTGTACCGAGACCT | 64326 |
rs546322788 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176026703 | TATAGTGACATGGTT[A/C/T]AAATTATGCATTTCC | 64326 |
rs546322869 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176061240 | CTCACATATATACAG[G/T]CAATTCATTTTAAAC | 64326 |
rs546344507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176123961 | ATCTACCTCAAACCT[A/G]ATCAATCAGATTTTA | 64326 |
rs546345036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176203637 | AAAATGTATCCAATG[C/T]CAAGCTAAATACTAC | 64326 |
rs546348768 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:175978402 | ATCTAATGCAACAGA[C/T]GTTTTCCCAGAGGCT | 64326 |
rs546353389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176185691 | ATGAAGACAAAAACC[C/T]TAAGCTAGGAAGAAA | 64326 |
rs546359624 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176007679 | GGGGTCAGGGACCCA[C/T]TTGAGGAGGCAGTCT | 64326 |
rs546368583 | in-del | -/T | 0.0228947 | 0.104514 | intron-variant | RFWD2 | GRCh38.p7 | 1:176174559 | AGCGATTTTCCTTCA[-/T]TAAAAAAAAAATTAC | 64326 |
rs546387890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176157468 | CTATATGAAACAATG[C/T]TTTCCAGACAAAGGG | 64326 |
rs546402483 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175960996 | TAGACAAAAAGGGAG[C/G]AGAAAGGTGAATTTG | 64326 |
rs546416320 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175955050 | TCCAGGAGTGTGAGA[C/T]CAGCCTGGGCAATAT | 64326 |
rs546436280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176097976 | GTGCCTTTCAGTTCA[C/T]GTGACTTTAATCTTT | 64326 |
rs546447747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176062641 | AATTTCAGGTATTCA[C/T]CCAAAGAAATAAATA | 64326 |
rs546483635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175984618 | GACCCCAAAATGGTA[A/G]ATCCACTGACAGCTT | 64326 |
rs546490626 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176185026 | AGAAAGCTCTACCAT[C/T]GTTTTCCATCACATG | 64326 |
rs546497671 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176098737 | GCAAAATAAATAACT[C/T]ACCTGGAATAATTTG | 64326 |
rs546511635 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176110163 | CTTAGATTCAACCAA[A/T]TTTTCGAAATTCTCC | 64326 |
rs546524150 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176090374 | GGTCACTCATTTTGG[C/T]TTTTTCGGCTCCAAA | 64326 |
rs546533515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176055360 | GAATCGCTTAAACCC[A/G]GGAAGAGGAGGTTGC | 64326 |
rs546538662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176152802 | CTACTTGGGTTCAGA[C/T]TCCCTACCTATAAAA | 64326 |
rs546544349 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | RFWD2 | GRCh38.p7 | 1:176008599 | AAGCCCTATAGCTAG[A/G]ATAATTTCTACTAAG | 64326 |
rs546551176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176198539 | GTTTTCTAATTTCAT[A/G]TTAGATAACTTCTTA | 64326 |
rs546554762 | snp | A/C | 0.0322114 | 0.122752 | intron-variant | RFWD2 | GRCh38.p7 | 1:175973783 | TTTGTGGCTACAAAA[A/C]TCAGCATTGTGCAAA | 64326 |
rs546576057 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176006195 | TTTTTGTTTTCCATT[G/T]GCTTGGTAGATCTTC | 64326 |
rs546580321 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175969195 | ATCCTTTTAGACATT[C/T]AATTTCTCCAAATAT | 64326 |
rs546611639 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176110538 | ACTTTTGCTATAAAT[A/T]TCTTACCAACTAGAT | 64326 |
rs546614658 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176191832 | ATCTGTCTCCATCAA[A/G]ACCTGTGTTTAACAT | 64326 |
rs546650831 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176018496 | CTGCTCAGCTTAAAG[C/T]ACAAGTAGGAATCAG | 64326 |
rs546661964 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | RFWD2 | GRCh38.p7 | 1:176005709 | TGATTGCACTGTGGT[A/C]TGAGAGATAGTTTGT | 64326 |
rs546663924 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176010159 | CCCCAAACACACACC[A/G]CCTCTTGTCTCTCTC | 64326 |
rs546669924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176068429 | CCATCAATCTGTGTT[C/T]CAACAAGATCTCCAG | 64326 |
rs546672837 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175964179 | CAGCTAATACTTAAT[A/G]GTGATAGGAGGCAAA | 64326 |
rs546691706 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176144725 | AGAAACAGACCCACA[C/T]ATACATGGACACATG | 64326 |
rs546701319 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176096241 | CACTTTCGCTTCTGA[A/G]CCTTTTGGTCCTATG | 64326 |
rs546703791 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176061161 | AGACTCACATATATA[C/T]AGTCAATTCATTTTA | 64326 |
rs546710501 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176019261 | CGAGGTCAGGAGTTC[A/G]CGATAAGCCTGACAA | 64326 |
rs546711549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175986419 | ACCCAGTAGCATAAC[C/T]GTCTCATCAATATAC | 64326 |
rs546714610 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | RFWD2 | GRCh38.p7 | 1:175944411 | AGCAATGGACTAGTT[A/G]GTTTGGTATACATTT | 64326 |
rs546722143 | in-del | -/GA | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176107016 | GACAAAGAATATTGT[-/GA]GACTGAATTCTCTGG | 64326 |
rs546732018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176205387 | TAAAGACATCATTTT[C/T]CTGCAGGAACTAGAA | 64326 |
rs546756954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175979357 | AAGCAGACTGGAATA[C/T]AGTATTGCATGGCTT | 64326 |
rs546767871 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176130372 | TCTCTAATTTTCTCA[A/T]TATTTCACACACACA | 64326 |
rs546801302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176138952 | TTGAAATTTTTATTT[A/G]AACAAATGCTTTACT | 64326 |
rs546803287 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176002342 | TGATTCTTTCTTTTT[A/T]AGTTTTTATTTATTT | 64326 |
rs546804675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176165833 | GTGAAGGGCCTGAAC[C/T]GCAGATACCTTACAC | 64326 |
rs546832481 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176145507 | ATTCCACTTCTAAAT[A/T]CATTCCATATAAATA | 64326 |
rs546840944 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175951331 | ACAGTTATTCACTCA[C/G]CAACTGGTGGATTTA | 64326 |
rs546854636 | in-del | -/AG | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175952012 | CTGAAGACAAGAAAC[-/AG]AGAAAATCTGTAGAA | 64326 |
rs546861866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176129073 | AATTTCTTAATATAG[C/T]CCAGAAGCTATTATG | 64326 |
rs546864579 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176002585 | TTGTTCAATTCCCAC[C/T]TATGAGTGAGAATAT | 64326 |
rs546870081 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176039488 | AACCACATGAGAAAA[A/T]TCAATGAAACAAAAG | 64326 |
rs546874147 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176125104 | TTAAATGATTATTCG[-/A]TTTTTTTTTTCCTAT | 64326 |
rs546874161 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176077648 | TACTGAAGGTCCTAA[C/G]CAGAGCAATCTGTCA | 64326 |
rs546891235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176007048 | AGGCTTTGCTCATTT[C/T]TTTTTATTCTTTTTT | 64326 |
rs546891855 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176172315 | CCAAAGTGTTAGGAT[G/T]ATAGGTTTGAGCCAC | 64326 |
rs546893480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176097570 | CTCTTTTTTTTATAG[A/G]GCTTTTTTTATAGAC | 64326 |
rs546906688 | snp | A/T | | | utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175944928 | CCACCAAGAGCAGCA[A/T]TGTCCATGGAGTTAC | 64326 |
rs546912242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175974227 | GATGGATTCAATATA[C/T]ATTAAAGGAAAAACA | 64326 |
rs546929387 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176129724 | CACAGAAGAGACTAA[C/T]AACTCACCATTCCAA | 64326 |
rs546932197 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176104907 | TCATTATATAACAAA[C/G]TGATTAAGTAAATTA | 64326 |
rs546935478 | in-del | -/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176038700 | GCGTGCGCCTGTAAT[-/C]CCAGCTACTCAGGAG | 64326 |
rs546937089 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176001785 | CTTATGGGGTAGGTC[G/T]CCTGACAAAGAACTC | 64326 |
rs546945978 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176100251 | AAAACTTACCAGGTG[G/T]GGAGGCAGGCGCCGG | 64326 |
rs546949852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176080997 | AAGAAATTTGGCATA[C/T]AGAAGCTCAGGAACT | 64326 |
rs546959597 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176047118 | ATAACCAGCTGGAAA[G/T]CTAATTAGCCCAAAG | 64326 |
rs546962841 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176137893 | GAGAAGAACAGGATC[A/G]AAAAACAACTGTAGC | 64326 |
rs546968523 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175965787 | CGGGGTTTCATCATG[G/T]TGGTCAGGCTGGTCT | 64326 |
rs546974547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176004176 | TTGGTGTGTAAGAAT[A/G]CTTGTGATTTTTGTA | 64326 |
rs546983221 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176190873 | ACTGTCTTATAGTAG[C/T]ACTGGTTCCAACTAA | 64326 |
rs546985715 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:175958827 | TTAAATTCATAAATC[A/G]ACAGTCAAAAATATT | 64326 |
rs546994327 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175995452 | AAAAAATTAATGAAT[A/C]CAGGAGCTGGTTTTT | 64326 |
rs547019746 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176001311 | AGGCATCAAGTATTT[C/G]AGTACGATGTTAACA | 64326 |
rs547023052 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176040222 | ACAATTTTTCTTTCT[G/T]TACTTTCTTGCTCTT | 64326 |
rs547031834 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176029203 | AATTTTTATGTAGTA[A/G]TTCAGTTATACAACT | 64326 |
rs547033582 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176150787 | TTGTAGAAAGAAGGA[G/T]AAAGTCCCCAAAATG | 64326 |
rs547045373 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176043096 | GACTGACATGAGTTT[C/G]AGTAAATATTTGTAT | 64326 |
rs547053035 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176048424 | GTAAAGTATGATACT[A/G]TAGCAATGCAGTAGA | 64326 |
rs547085335 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176156627 | ATGGAAACATTAACT[A/G]TAAGTAAGATGCTGT | 64326 |
rs547093212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175972145 | ACAACAACAAATACA[A/G]AAGGTGGTTCTTGGT | 64326 |
rs547116132 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176190194 | TGCATTTTGAAATAT[G/T]TGCATTTATATTCTT | 64326 |
rs547119678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176144055 | TCAGCATCAAGACTA[A/G]GATGCCCCGCTATCA | 64326 |
rs547145238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176030391 | CAATAGATAAGTATG[A/G]AGCACTTACTGTGCC | 64326 |
rs547157562 | in-del | -/T | 0.00636936 | 0.0560724 | intron-variant | RFWD2 | GRCh38.p7 | 1:175991735 | AAAAGCTTTTTAAAC[-/T]TTTTTTGTTAAAAAC | 64326 |
rs547178798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176075420 | TAGCAATATTTGACA[C/T]GTTAAAACTTACCAA | 64326 |
rs547191331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176081712 | TTTGTTTAAAATCCC[A/G]TTTATAATAACATTT | 64326 |
rs547206288 | snp | C/T | 1.6528e-05 | 0.00287467 | missense, intron-variant, utr-variant-5-prime | RFWD2 | GRCh38.p7 | 1:176162942 | AAATCAAGGTTATCT[C/T]GGTCAGTTCCCAACC | 64326 |
rs547206402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176023421 | AAAATATGAATTCAC[C/T]TAGAAAAAGTAAACA | 64326 |
rs547209228 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175982831 | CTTAAAAAATTGAAC[C/T]CAGAGAAATAGAGAA | 64326 |
rs547223976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176140949 | TTAGAAACATTTAAC[A/G]TAAAGGTAAAGAGTA | 64326 |
rs547224018 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176159202 | CACACACACATACAC[A/C]AATCAGTAAGAGAAA | 64326 |
rs547229624 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176169286 | TACATTCACTATAGA[A/C]TTTTATGTCTAAGAC | 64326 |
rs547244746 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992309 | AGTCTACAGCTCCCA[C/G]AGTGAGCGACGCAGA | 64326 |
rs547260138 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176177874 | TTGTTACTTTCAAGA[C/T]AAGTAAAAAGGAGGA | 64326 |
rs547270857 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176164962 | AGCATAAGTAACTTA[C/T]GCATGGTGACATATA | 64326 |
rs547278601 | snp | C/T | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176185508 | TTAGGATTGGCTATA[C/T]GATATTATTCTGGCC | 64326 |
rs547286367 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176072488 | AATCCCTCCCTCTGC[A/C]CTCCCATTCATCTCA | 64326 |
rs547295937 | snp | A/G | 4.95381e-05 | 0.0049766 | intron-variant | RFWD2 | GRCh38.p7 | 1:176081110 | TTCAATTAGATTCTA[A/G]ACATTCTTACAAAAG | 64326 |
rs547297323 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176126208 | ATCTGGATGCTCTTT[A/C]TTTCTTTCTCTTGTC | 64326 |
rs547299511 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175966207 | TTAAACTAAAATGTT[A/G]GTTAGCCTTCCCTGC | 64326 |
rs547307735 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176113184 | TATAGGGGCATTCAC[A/T]CTTTCTCCACGTCCT | 64326 |
rs547326517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175993637 | TGAACTGGAAGAAAG[A/G]GTATCAGTGATGGAA | 64326 |
rs547330225 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176161524 | AATCACTTGAGCCCA[C/G]GGGGTAGAGGATGCA | 64326 |
rs547334912 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176187798 | GGCAGAATACACCAA[A/G]AAGAGAAAATACGGG | 64326 |
rs547353642 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176036921 | TTTGATGCCCATAAA[A/T]CTTGTAACAAATAAA | 64326 |
rs547356549 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176084343 | AGTTACTTTTTCCAA[C/T]GAAATAAGAGGACAC | 64326 |
rs547370228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175962754 | CAGCCATCTCTCACC[A/G]CACCTCCCCCTCCCT | 64326 |
rs547405521 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176137454 | TCCAGAAACACTATA[C/G]CAATTTAAATTCCTA | 64326 |
rs547414174 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176093443 | GCTGGGCATGGTGGC[G/T]CATGCCTGTACTCCC | 64326 |
rs547429542 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176110880 | ATTTATCAGCAGGGC[A/G]CAGTGGCTCATGCCT | 64326 |
rs547429713 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176173758 | TTTGGGAGGCTGAGG[C/T]GGGAGGATCGCTTGA | 64326 |
rs547430957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175955075 | CAATATGGCGAAACC[C/T]TCTCTATCAAAAACA | 64326 |
rs547436687 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176183884 | GAGGTATCTAGAATA[C/G]TTAAATTAATAGAAA | 64326 |
rs547444530 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175975594 | TTTGTATTTTTAGTA[C/G]AGACAGGGTGTTGCA | 64326 |
rs547468267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176083550 | GGTATATCACCTCTC[C/T]TATCCTAATTACAAA | 64326 |
rs547490674 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176168000 | ACGTTGCAAGCATAC[C/T]GTATTTTTTATTAGT | 64326 |
rs547506880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176118629 | TGTGTGGTGGTGGAC[A/G]CCTGGGGTTCCAGCT | 64326 |
rs547517864 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176148141 | TTTGTTAGTAGGAAT[A/T]TTAAAATCACAACTA | 64326 |
rs547518488 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176187074 | CTATCAAATCAGTTA[A/C]AGCCAATAGCTTTTA | 64326 |
rs547525902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175997226 | ACTGGATCCCTTCCT[C/T]ACACCTTATACAAAA | 64326 |
rs547548727 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176002223 | TACAAATGTTGGCAT[C/G]CTTGATGGTGTCTCC | 64326 |
rs547561498 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176050756 | CAAGCATTGTTTTAA[A/C]CACCTTACATAAATT | 64326 |
rs547565035 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176085005 | TGTCTCTACTTCATA[A/G]ATGAGCAAAGACACT | 64326 |
rs547571121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176175848 | TTCTGAATAAATTAG[C/T]GCTAGCACACAATTT | 64326 |
rs547577711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176112426 | CATTCAATTTCTTTT[C/T]AGAAAAGTTGCTATA | 64326 |
rs547578005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176105892 | ACCACCTTTGCAAAA[C/T]TATGACTAAGACAGT | 64326 |
rs547585535 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176078784 | AATCTACAAGAAACT[A/T]AAAAAAAAATCAACC | 64326 |
rs547586313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176169982 | TTCACAGCATCTTCA[C/T]TAGGAGTAGATTTCA | 64326 |
rs547596195 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176007929 | TGGGTAATGGCGGGC[A/G]CCCCTCCCCCAGCCT | 64326 |
rs547601705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175953264 | CTAATAAGCTAGTAA[A/G]GGAGAAAAAATATTA | 64326 |
rs547603527 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176120689 | TAGATTATTTTCCTT[A/C]AAAAGCAAAGACGTA | 64326 |
rs547614368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176106547 | GCAGACCCTGCACTT[A/G]ACAGATCAGCTGGCA | 64326 |
rs547632564 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175963777 | CCAAGTTAGAAGTAA[C/T]GTCTTCCCTCTAGGG | 64326 |
rs547638476 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:175990005 | TCTCTATCACTAATT[C/T]CTACTCTAACCTTTA | 64326 |
rs547647398 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207141 | TTTTTAAGGCAGCCA[A/C]ACAACAGCGTCCCAC | 64326 |
rs547649742 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176043658 | AAGTTCTAAAAGTTT[G/T]AACAAACCAAATGTA | 64326 |
rs547673007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175988602 | ATTTGGTAGGCCGAG[A/G]CAGGTGGACCACCTG | 64326 |
rs547680183 | in-del | -/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176000730 | TACATGCAATGTTGC[-/T]TTTTTTTTTGTTATG | 64326 |
rs547683969 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175993998 | GCAGCCAGAGAGAAA[C/G]GTCGGGTTAACCACA | 64326 |
rs547685709 | snp | G/T | 0.000172043 | 0.00927318 | intron-variant | RFWD2 | GRCh38.p7 | 1:175982399 | TTCCTCTTCTACCAC[G/T]CCAGAGAAAGACCAA | 64326 |
rs547697901 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207436 | GAAAACGTGCCAGAG[A/G]GCAGGCCGTCTTAAT | 64326 |
rs547704174 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176111936 | CAACAACCAGCCAGT[C/G]CTCTAACAGATGCTA | 64326 |
rs547724327 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176167146 | ATTCAAATGTCTATA[C/T]ATGTATATATGAAAG | 64326 |
rs547741803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175956122 | AAAAGCATTAGGAAT[C/T]AATACAGTGTAGTAT | 64326 |
rs547745366 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176191570 | ATTCAGGACTGAAAG[-/A]AAAAAAAATGAGTAA | 64326 |
rs547754832 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176080980 | ATTCCACTTTAGAGA[C/T]GAAGAAATTTGGCAT | 64326 |
rs547757366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175954025 | TGCATGCGTACTAGT[C/T]CCCAACAAAGATGTG | 64326 |
rs547768543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176036054 | CAAACAGAATTTTAA[A/G]CAGAATGGAAAAGCA | 64326 |
rs547773608 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176071084 | ATCTCATATTGAACT[G/T]GTAATCCATAATGCT | 64326 |
rs547795322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175945967 | AAATCTTAGATTTGT[C/T]AGTGGGATCCTATGA | 64326 |
rs547797505 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:175993239 | CACACCAAAAACCCA[C/T]CTGTATATCACCACC | 64326 |
rs547803143 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176021849 | GAGAAGCATAAAAAA[C/T]CATTTTAAGTAAATA | 64326 |
rs547809020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175984981 | GGCAGAAGGGACTTG[A/G]CTTATCTCAGATGAA | 64326 |
rs547812717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176063743 | GGGCATTTTTGGGGG[A/G]CTCTGTTTGATAAAT | 64326 |
rs547831086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176032452 | CTAAAGCTTAGCTAC[C/T]TAAAACAGCAAACAT | 64326 |
rs547851960 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176091124 | AAAAAATTTCAGCCT[A/C]AAATTCAGAACCCCA | 64326 |
rs547861800 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176112870 | GACCTCCAGTTCCAT[C/T]CATGTTGCTGCAAAT | 64326 |
rs547865074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176080589 | GAGGGAAAATCATCA[C/T]ACAATCCAAAGATAT | 64326 |
rs547878194 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176124728 | CAGTGCTGCAACAAA[C/T]ATGGGAATGCAGATA | 64326 |
rs547884622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175997671 | CATCACTGGCTATCA[A/G]AGAAATGTAAATCAA | 64326 |
rs547902555 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175991785 | CTAGGTCTACACAGG[C/G]TCAGGATAATCAATA | 64326 |
rs547921690 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176131885 | CACTCTTGAAGAAAA[A/T]ACTGTTTGCCTATTT | 64326 |
rs547925898 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175953642 | AATACAGATAAGATA[A/C]ACCACGCAAACATTA | 64326 |
rs547936394 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176102844 | AACTGGCTCATCTGA[A/T]CTTGTGGCCCTGGCC | 64326 |
rs547947362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176193346 | GTAATGCAGCTACTA[C/T]GGAAAACTGTTTGGC | 64326 |
rs547960613 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176087823 | ATGTTTATTGCAGCA[C/G]TATTCACAATAGCAA | 64326 |
rs547966694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176022392 | AACTCCAAAAGCAAT[A/G]TTTAAGAAAAGTACA | 64326 |
rs547967599 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176197533 | TTTAAGCCACCTAGT[C/G]TGTTGTATTTTGTTA | 64326 |
rs547970024 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176061485 | TACAAAATTCACTAG[A/G]CATGGTGGCGTGCGC | 64326 |
rs547983274 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176006299 | GGTCTTGACTCTTTA[A/T]CCAATTTGCCAGTCT | 64326 |
rs547992553 | in-del | -/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176087386 | CTAAAATCTAGAATC[-/T]ACAAAGAACACAAAG | 64326 |
rs548001863 | in-del | -/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176065706 | AAGGGGATAATGATT[-/G]TTTTTTTTTTTTTTT | 64326 |
rs548021130 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176039279 | AAATAAAAATACAAT[G/T]TATCAAAATTTGCAG | 64326 |
rs548030799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176056708 | TAAATTTATCAATCA[C/T]GTTTACTTTTGTATC | 64326 |
rs548032700 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176154222 | TGATTTAATTTTGGA[C/G]CTCTTTATTGGTCTG | 64326 |
rs548038659 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176058431 | TGTACTAAGAAAAAT[A/T]CTTATCCTGTTGATC | 64326 |
rs548040625 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176179861 | CACTATCTCTCAGAC[-/A]AAAAAAAAAAAAAAT | 64326 |
rs548047356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176168304 | CCTCGTGATCCGCCC[A/G]TGTCAGACTCTCAAA | 64326 |
rs548051020 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176023423 | AATATGAATTCACCT[A/G]GAAAAAGTAAACAGG | 64326 |
rs548053869 | snp | A/G | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176185290 | CTAGGCACAGTTTAT[A/G]GATGAGGGAACAGAA | 64326 |
rs548083609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176200027 | GTTAAGAACCTGACC[C/T]CTGAGCCAAATTGTC | 64326 |
rs548088764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176161213 | TTTTATTTATTTTTG[C/T]CTCTTTAAAATCCCT | 64326 |
rs548101681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176196991 | AGCAATAATACCTAT[A/G]TTACGGGTTAAATTG | 64326 |
rs548101887 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176071804 | TGTGACAAACCTTCA[C/T]AAGTCTACTAAAATT | 64326 |
rs548110139 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176061120 | AGGAGACATACAGAT[A/C]AATACAACAGAACAG | 64326 |
rs548112090 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176183677 | CAGCAGCATTATTCA[C/T]AGCAGCCAAAAGGTA | 64326 |
rs548137963 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176143396 | AACAATCACAGGTCT[-/A]AGACTGCTTCTCCAG | 64326 |
rs548143189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176153713 | CCCATTTAATGATGT[C/T]GGCTGTGGGTTTGTC | 64326 |
rs548146342 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176174824 | TAATCCCAAGAGTGC[C/T]CTACTTCATGCCTAC | 64326 |
rs548149243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176161806 | CGACCTCCCAAACAG[A/G]TATAACATGGGAGAC | 64326 |
rs548157508 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176102907 | AATTCCCCATGATTT[A/C]ATCTCTGACCCAACT | 64326 |
rs548164816 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176024685 | CAGATATGATTCTAC[G/T]TGTAGAAAACCCCAA | 64326 |
rs548168593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176165612 | AGGAAGGAGAATCAC[C/T]TGAACCCAGGAGGTA | 64326 |
rs548202199 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176115358 | GGGAGGCTGAGGCTG[C/G]AGAATCGCTTGAACC | 64326 |
rs548203369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176122439 | ATTTCCAAAAAAATT[C/T]TGGAAACTTATATAT | 64326 |
rs548218723 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175994751 | TTCATAAAGCAAGTC[A/C]TGAGTGACCTACAAA | 64326 |
rs548222357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176068043 | CTCTGGTGGGGAATG[C/T]TGGTAATGGGTGATG | 64326 |
rs548225982 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176025358 | TATAAACAGAAAACC[C/G]AAACACTACTAAAAA | 64326 |
rs548226168 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:175966627 | TCATCCTGAATTTAT[C/T]AAAGCAAAATGGAAG | 64326 |
rs548246785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176038742 | AGAATCGCTTGAACC[C/T]GGGAGGCGGAGGTTG | 64326 |
rs548270965 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175950892 | TAGTGAAGAAAACCT[C/G]CATCTACTAAAATAG | 64326 |
rs548275657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176195769 | GTCCATTATCCTAAA[C/T]GGATTAACACAAAAA | 64326 |
rs548276449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176127968 | CATTAATTTGCATTT[C/T]TCTGATGATTAGAGA | 64326 |
rs548303022 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176161095 | CTTAGCTTTCTCCCT[A/G]TTGCTGGTGTAGCAT | 64326 |
rs548305463 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176024015 | GTAATCCAAGCACTT[G/T]GGGAGGCCGAGGCAG | 64326 |
rs548307113 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175979733 | CATATGAATGGTTCA[C/T]GTCAGCAAAACTGCT | 64326 |
rs548312357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176128898 | TGGTCATAGGTAATA[A/G]TCCAGCCAAAGACTC | 64326 |
rs548313944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176121723 | ATCTTCTCTCATTGC[C/T]TGTTTAGAAACAGAC | 64326 |
rs548329611 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175957497 | TATACCATCCAGGTT[G/T]GGGAAGTACACTCTA | 64326 |
rs548340514 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176026157 | TAGCGGAAGCATTTT[C/T]AAAGTAGGTTCCTAT | 64326 |
rs548401232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176183143 | TTTTAAGTGACTAGC[A/G]GAGGGAATACACCTA | 64326 |
rs548403106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176176636 | CCAGCCTGGGGAACA[C/T]AGCAAGACTCCATTA | 64326 |
rs548412352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176190992 | GAAAAACAAGCAGTA[A/G]TTACACCTCACATAA | 64326 |
rs548416508 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175987678 | ATATTTGCTTTGGCA[C/G/T]TCTCATACATATGTG | 64326 |
rs548420885 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176016150 | TAGAAATGTCTGGAG[A/T]TTTTTTTAGCTAAGA | 64326 |
rs548424199 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176151350 | GAAGGAAGGAAAGAA[A/G]GAAAAAGAAAGAAAG | 64326 |
rs548488677 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176085562 | TCTAGCTTGCCATAT[A/G]AAGATTCAGAATTCA | 64326 |
rs548521062 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176011849 | TTCTAAGTTTTTGGT[C/T]ATTCTGGTGTACACA | 64326 |
rs548527165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175977572 | AATGGAATAAGAGAT[A/G]AAAAAGGTACAAATC | 64326 |
rs548530137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176018427 | TTAAAAAACCCAGTC[C/T]TCCCTCACCTAATTT | 64326 |
rs548536363 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176150836 | GGGTCCAACTACATA[A/C]ACCAGGAATTCACCA | 64326 |
rs548539982 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176001900 | TTTTCCTTTCAATAC[G/T]TTAAACATATCCTAC | 64326 |
rs548546467 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176158611 | AGAGAGAAAATGAAA[C/G]TATACTGTTTTTAAG | 64326 |
rs548552637 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176052479 | ATCGATTTTAAAGAC[C/T]GAATTAGGATAAATT | 64326 |
rs548556081 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176142218 | AACCACTAAAAAATG[A/G]TACAAAAAATTTACT | 64326 |
rs548565580 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176008979 | GAGCTTAAATCTGCC[G/T]TAGCCTTCACTTCCT | 64326 |
rs548581327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176094571 | GTTAATTTTACCTAG[C/T]TTGGTTCTAAAGAAA | 64326 |
rs548588319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176145947 | CATTGTGCTTACAAT[A/G]GTGGTTATACAAATG | 64326 |
rs548589289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176203173 | AAACCCCGCCTCTAC[C/T]AAAAATACAAAAAAT | 64326 |
rs548643643 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176163494 | CCAAAGTGTTGGGAT[C/G/T]ATAGGTGTGAGCCCA | 64326 |
rs548645203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon | RFWD2 | GRCh38.p7 | 1:175971973 | AAAGAATAGGTTTGC[A/G]GCAGCGACTGTTGGA | 64326 |
rs548652624 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176208480 | TTTTTCATTTGCCGC[A/G]TTCTAAGGGGTGGGA | 64326 |
rs548658563 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175974861 | AATATGGGTGGTCAA[C/G]GCTGCAATGAGCCAT | 64326 |
rs548682152 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176113591 | TGGAAACCTTTTCTT[G/T]TTCCCCTATATAAAG | 64326 |
rs548691375 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175990534 | AGTCTTCTAAAACTC[G/T]GCCAATTTTCTGTCC | 64326 |
rs548699419 | in-del | -/ATAA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175958676 | TCAGAATGAGAATAA[-/ATAA]TGTTATAGAAAAAAG | 64326 |
rs548701551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175984331 | CCATGGCTTCAGAGG[A/G]TGCAAGCCCAAAGCC | 64326 |
rs548703221 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176007461 | TGTTCTGTTTTTTTC[C/T]CATCTTTGTGGTTTT | 64326 |
rs548719562 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176056069 | CCATTTTGATCCCAG[C/T]GTTGCCAAAAAAGCT | 64326 |
rs548724354 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175953304 | TCAAAAAAAAGAAAG[G/T]AAATGAGGAACATAG | 64326 |
rs548725050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176202506 | ACTTTTTAATAGTCT[A/G]AAAAACAGAGCCACG | 64326 |
rs548726287 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176055446 | ATCTCAAAAAATAAA[C/T]AAAACAAAACAAAAG | 64326 |
rs548737048 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176029836 | TTAATATGTGAAATC[G/T]CCAAGTAGAAATTAA | 64326 |
rs548738092 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176180206 | ATGTTTAGCACAATA[C/T]CCTGTTAAAAGAATT | 64326 |
rs548775957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176000223 | GTTTTCTTGTAGTAG[C/T]TTTGTAGTTTGAAGT | 64326 |
rs548776090 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176005613 | TTTCGTTATGTACCC[A/G]GTAGTCATTCAGGAG | 64326 |
rs548796625 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176173805 | CCAGCCTATCCAACA[C/T]GGTGAAACCCCGTCT | 64326 |
rs548821341 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176146818 | ATAACTAATGCAAAT[A/G/T]CCTATTATGTGCCTT | 64326 |
rs548827353 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176049035 | AAATTAGCCAGGCGC[A/G]GTGGCGGGCGCCTGT | 64326 |
rs548845162 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176183762 | TATACAATGGAGTAT[C/T]ATTCAGCCTTACAAA | 64326 |
rs548847697 | in-del | -/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176088021 | GAAAACCAAACACCA[-/T]TATGTTCTCACTCAT | 64326 |
rs548864470 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176005146 | TATTTGTGTAGAGGT[G/T]TTTGTAGTATTCTCT | 64326 |
rs548871092 | in-del | -/AG | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176176380 | ATACCCTTAATACTC[-/AG]AGTTCATTGAAATAA | 64326 |
rs548880973 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176101719 | TATTTTGTTTTGATA[C/T]ATGTTTTCTAATAAC | 64326 |
rs548888193 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176131965 | TGACAGCTTTGCAAG[A/C]AATTTTAGCAATTCT | 64326 |
rs548909833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176143060 | CAAAGTCAAAAGTTA[A/G]TTATTAGAAAAAAAC | 64326 |
rs548914527 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176140902 | AATAGCAAGCACTCT[A/C]TTAACACTGTGCCAA | 64326 |
rs548923571 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176064524 | TATCAACATTAGTTA[C/G]CACACTCTAATACAC | 64326 |
rs548932299 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176195161 | GGAGAAGAGAGGGAA[A/G]GAGGAAGGGAGGGAG | 64326 |
rs548942222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176001849 | TTCATTTTTGATGAA[C/T]AGTTTTGCTGAATAT | 64326 |
rs548960055 | in-del | -/A | 0.145034 | 0.226897 | intron-variant | RFWD2 | GRCh38.p7 | 1:175961911 | ATGGAATAAATTTGA[-/A]AAAAAAAAATGGTTT | 64326 |
rs548964423 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175974360 | TAGGACTGTGCTTAA[A/C]ATTTTAGAAATTTAA | 64326 |
rs548984824 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176199793 | ACACAGAGTATGAAG[C/T]GCTGGCAAAAGTGAA | 64326 |
rs549005447 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | RFWD2 | GRCh38.p7 | 1:176002153 | TGCAAAAATACTGGC[C/G]ATCATTTCTACAAAT | 64326 |
rs549014235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176062023 | ATTGTTTTTGGAGAC[A/G]GCATCTCACTCTATC | 64326 |
rs549022039 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176195360 | AACTAAAAGGAGACA[C/T]AGCCAAATCTAGTTA | 64326 |
rs549022465 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176205060 | GAATGACAATGATCG[A/C]TTCCTTATTCCTCAC | 64326 |
rs549039944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176098135 | TTTGGTTTTTGAGAA[C/T]GATCTAACTTGATGG | 64326 |
rs549046484 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176096799 | AGCCAATCTGGTCTG[C/G]TTTACATAACTTTCT | 64326 |
rs549060040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176206341 | CCTCCTCAGCAACAC[C/T]TACCTACCTCTTTAT | 64326 |
rs549061585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175987829 | TTATTTAAATTTGTA[C/T]AAATTATCAACAATA | 64326 |
rs549070356 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176167890 | AGCCTGCCATAAGGA[C/T]TGACTTCATGTACAT | 64326 |
rs549081490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176184858 | TATTGAACTAAACTT[C/T]AGGGGATTGTTGGTA | 64326 |
rs549097063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176070240 | GAAGTTCTGGCTACC[C/T]TAGTTCTTATACATT | 64326 |
rs549116033 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176026980 | TAAATACAATGGTAC[A/T]AACGGTGTGAACTAG | 64326 |
rs549122820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176096536 | CATGGTTGACTGGCC[A/G]GACTACCATTGGTCT | 64326 |
rs549126180 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176008637 | TTGTTTGTGTATACC[-/T]TTTTTTTACTGAAAA | 64326 |
rs549133639 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176165751 | AACAAGGGTCAGAGT[A/G]ATCTTGTGAATGATT | 64326 |
rs549165097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176124624 | TTTTATGGCTGATAG[C/T]ACTCCATTGAGTATG | 64326 |
rs549171706 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176006605 | TTTCTCCTTTGCTTA[C/T]GAAGCTTAGTTTGGC | 64326 |
rs549183572 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176019898 | GTTACAGGAAACATT[G/T]ATTTCCAATATGATC | 64326 |
rs549184731 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175997384 | AATGGCAACAAAAGC[C/G]AAAATTGACAAATGG | 64326 |
rs549192698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176180718 | AAGGATGAGTAGATA[C/T]AAACAACTGTAAGTA | 64326 |
rs549218788 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176191629 | CTCTTCTTTACACCT[A/C]TACCGATAACACTAG | 64326 |
rs549221193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176056479 | TAGACTTAAACTTCA[A/G]TGCAGACTGAACTTT | 64326 |
rs549223281 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176007825 | CTGTCCCCAGAGGTG[C/G]AGCCTACAGAGGCAG | 64326 |
rs549236338 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176175394 | CATAGAGAACAATTC[C/T]TCCAGACTGAAGGGA | 64326 |
rs549253515 | snp | A/C | 0.084364 | 0.187256 | intron-variant | RFWD2 | GRCh38.p7 | 1:175966316 | ACACACACACACACA[A/C]ACACTTAAAAACCTG | 64326 |
rs549264553 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176002687 | CAAAGGACATGAACT[C/T]ATCATTTTTTATGGC | 64326 |
rs549294537 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | RFWD2 | GRCh38.p7 | 1:175944605 | ATCTGGTCAGAGAAT[G/T]AAGAAAGAATTTTAT | 64326 |
rs549325318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176088862 | TAGCCAGGCATCGTG[A/G]TGCATGCCTGTAATC | 64326 |
rs549326927 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175955963 | TTCCAATTAAAATCA[C/T]ACAAACTTTTCTAGT | 64326 |
rs549331150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176167050 | TGTTTCCTCATCAAG[A/G]GGTATTTTATTATTT | 64326 |
rs549347400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175987253 | GGACTAATTAGAAAT[C/T]ATGTAAGAAAAGGAT | 64326 |
rs549350754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175959338 | CTACAAAACTCTTAC[A/G]GCAGACATACTTAAT | 64326 |
rs549362390 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176081737 | ACATTTTAGATAAAA[C/T]AGTTTATAAATAAGA | 64326 |
rs549371987 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176119797 | AGTACCATTTACTGA[C/T]GGTTTACTATGCACT | 64326 |
rs549404524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176082351 | ATGCCATCTGAAGTA[C/T]AGTAAGCATAATAAA | 64326 |
rs549405880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176000093 | CTGTTGCCTTCGCTG[C/T]GCAGAAGCTTTTTAA | 64326 |
rs549433253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176178737 | AGGCACCTGTAATTC[C/T]GGCTACTCGGGAGGC | 64326 |
rs549435851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175965829 | CCTCGTGACCCACCC[A/G]CCTCAGCCTCCTAAA | 64326 |
rs549473512 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176037275 | AGCCAGGCATGGTGG[C/T]GGGTGCCCGTAGTCC | 64326 |
rs549499442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176136779 | GTTGTACTTCTTTAA[C/T]ACAACAGTTTGATTT | 64326 |
rs549500719 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176047165 | TGAATCATCACATAC[A/G]TTATTCCTCAATATG | 64326 |
rs549513340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176166440 | AAGGTAGATCAAGCC[C/T]GTAAAGGCCACAAAA | 64326 |
rs549525710 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176009493 | AGGTTAAATTATGTC[C/T]TTGTGTACTGTACAA | 64326 |
rs549534783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176030468 | TGTATCGTTGTTTAA[C/T]GTTAATTAAATATAA | 64326 |
rs549554210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176116747 | CAACAGAAAAAGTAA[A/G]TCTAAAGTATATCAT | 64326 |
rs549562943 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176121606 | GGAATACTACTTTGA[A/C]AGTTGCAACTTGGAC | 64326 |
rs549572950 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176159486 | TAAGATTAAAATGTG[C/G]ACACATACCCTAATG | 64326 |
rs549586038 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176188592 | TCACTTCATATCTCT[A/G]TGTCACATTTTGGTA | 64326 |
rs549592315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175962871 | AAAAGCAGAAAAAAA[A/G]TTAAGTTGTGTACTA | 64326 |
rs549601845 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176114477 | TTCACTTAGATAAAA[A/C]TAGGTGTACTATTTT | 64326 |
rs549605793 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176001497 | AAAGTTGATATACTA[C/T]AGTGATGTAAAAATA | 64326 |
rs549613379 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176069308 | CTTTAAAATCAAGCA[C/T]AGAAAGAATAATCTT | 64326 |
rs549613415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176076320 | CAATATCAAGAAGAT[C/T]TCTCAAAACTACACA | 64326 |
rs549615475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992350 | TTTTGCATTTCCATC[C/T]GAGGTACCAGGTTCA | 64326 |
rs549622872 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176181599 | TGTAATCCCAGCACT[C/T]TGGGAGGCCGAGGCG | 64326 |
rs549627943 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176033355 | CTGCTTGAACCCGGG[G/T]GGTGGAGGCTGCAGT | 64326 |
rs549640638 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176140427 | AAAAGAAAAAAGTTT[G/T]GAAGACTGAAAACTG | 64326 |
rs549640931 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176111084 | CTGAACCCGGGAGGC[A/G]GAGGTTGCAGTAAGC | 64326 |
rs549651431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176133666 | TTAAGTAAATGCACC[A/G]TACTGTCACAATTTC | 64326 |
rs549668065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176163599 | AAGACAAATGTTTCA[A/G]TATAATCCTACCAGA | 64326 |
rs549675254 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176120772 | ATAATGAAGAGGTAG[C/G]CAAGAGAAAACAATG | 64326 |
rs549694830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176172436 | CTTTTCAAAATTTTC[A/G]TATGAGTTATACAAG | 64326 |
rs549697468 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | RFWD2 | GRCh38.p7 | 1:176096480 | GAATGAGCCACAGCC[A/G]CTGTCCAGGCCCCAA | 64326 |
rs549704566 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176202575 | TGGTGGCACCCGTCT[C/G]TAATCCCCGCTGCTT | 64326 |
rs549707137 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175988770 | CCTGGGGGGCAGATG[C/T]TGCAGTGAGCGGAGA | 64326 |
rs549708709 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176113654 | AAAAAAACACCTGTA[C/G]TTAAATAAATTTTAT | 64326 |
rs549723202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176024565 | CTAAACGCTCTTCAC[A/G]TATGATAAAAAGTTT | 64326 |
rs549726924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175952400 | GCACTCCATCCTGGG[C/T]GACAAGAGCAAGACT | 64326 |
rs549727011 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176075988 | AGCCTGGGTAACAAG[C/T]GCAAAACTCCATCTC | 64326 |
rs549734236 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176134199 | AACTGGACTTCCTGA[G/T]AGTACACATTACCTA | 64326 |
rs549747189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175946690 | TCAATTTTCAACTGA[A/G]CACTAAAATAACTTT | 64326 |
rs549754792 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176086802 | GCCCACATTGCCAAG[A/T]CAATCCTAAGCAAAA | 64326 |
rs549766791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175990024 | CTCTAACCTTTATTA[C/T]TTCCTTCCTTCTGCT | 64326 |
rs549777519 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176175323 | TGTTAAACCTCACAT[A/C]CAGTCTGTCATCTAC | 64326 |
rs549778260 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176113120 | TAGTTTTCTGAGGAA[A/C]CTCCATACTCTTTTT | 64326 |
rs549798842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175982505 | TAATAAACAGTAAAT[A/G]TATTTTCTTTTATGA | 64326 |
rs549815804 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176004732 | GGATAAGCTTTTTGA[A/T]GTGCTGCGGGATTCG | 64326 |
rs549820852 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175947810 | TAAAAGGGAAAAAGA[C/T]TGTCAATGGAAGAAA | 64326 |
rs549832299 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175970117 | CTCTCCAAGTTGAAG[C/G]AAGGAATGTACCTGG | 64326 |
rs549857633 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | RFWD2 | GRCh38.p7 | 1:175961104 | CTGGGACTTGCATCA[A/C]TGGGCCCTCAAATTC | 64326 |
rs549859175 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176188394 | TTAATTCTTTCCAAT[G/T]TTGAAGAACAAGAAT | 64326 |
rs549859822 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176174398 | TATCATCCTGCAAGG[G/T]ACCATGCCACTCAAT | 64326 |
rs549864440 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176168409 | GACAGCTGGGTGGGT[C/G]GGGGGAGTACGGGGG | 64326 |
rs549865499 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176051337 | TTAAGGACATCTTAT[A/G]TTCCCACAAATTATA | 64326 |
rs549888721 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176071173 | TGCTATCTTCATGAT[A/C]GTGAATTCTCGCAAG | 64326 |
rs549892543 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176078017 | CAAATAAATGGAAAA[A/T]CCTTCCATAAGCATG | 64326 |
rs549893758 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175963505 | CCTTATTTAGCTGTG[A/T]AATCTTGGGCAAATC | 64326 |
rs549903248 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207513 | GGTGGTTTGAAAGAC[A/G]GGAACGTAGCGGGCG | 64326 |
rs549907039 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:175946013 | TGAGCTCTTGTAGGT[A/G]TGCTGGCAATCCCAA | 64326 |
rs549927693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176162067 | AGAAAATCAGAGCTG[C/T]CCCAATCAAACAGGC | 64326 |
rs549942217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176112489 | TAATATTTTGATAGA[C/T]GTATACAATGTGTAA | 64326 |
rs549947449 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176141964 | GTCTTGAACTCCTGG[A/C/G]CCTCAAATGATCCTC | 64326 |
rs549951633 | snp | C/T | 0.000313183 | 0.0125097 | missense | RFWD2 | GRCh38.p7 | 1:176043789 | CTGCTAGCTAACAGG[C/T]TCTTATGGTAACTAC | 64326 |
rs549961441 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176170527 | GAGCAGTAGTATTTT[C/G]AAAGGAATCTTTTTT | 64326 |
rs549969121 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176164359 | TCCTACTCTTTTTCT[G/T]GATAATAACATGACT | 64326 |
rs549981937 | snp | C/T | | | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207302 | GGCGGAAGAGGCGGG[C/T]GTGGCGGGGGATACA | 64326 |
rs549985980 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175984437 | ATTTCAGAGGATGTA[C/G/T]GGAAACGCCTGGCTA | 64326 |
rs549999272 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176061830 | AATGGATGAACTGGA[A/G]TTCATCAAAATTAAG | 64326 |
rs550002314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176100430 | GAGAGAGATAAATTA[C/T]ATTTCAAGACTTATC | 64326 |
rs550014265 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176066365 | CAACTTATTCCACAG[C/G]CCCAGCCACTGAACC | 64326 |
rs550014326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176073723 | TACTGTCAAAGTAAA[C/T]AAATGCTGCCACCTT | 64326 |
rs550031988 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:175988630 | CTGAGGTCTGGAGTT[C/T]GAGACCAGCCTGGCC | 64326 |
rs550042052 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176079586 | CCAAGCCTCAGTGTC[A/G]TGCAATATACCCATG | 64326 |
rs550064307 | in-del | -/AAA | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:175982934 | TTCAGCTAATTAGAC[-/AAA]AAGAGTAAGTTTTTG | 64326 |
rs550067250 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176186797 | ACTAGGGTGGTAGTA[A/G]TTGGGTTGATGAGAA | 64326 |
rs550080288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176194192 | TGGAAATCTTAAAAA[C/T]ATCCAATTAATCCCA | 64326 |
rs550082208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176201608 | CTATTGCACAAGTAC[C/T]TTCTTCTCAATTTAT | 64326 |
rs550086517 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176195114 | AGAAAAAGGAGAGGA[A/G]AGAAAGAGGGAGAGG | 64326 |
rs550088878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176031096 | CCCCAGAGCCTTCAC[A/G]GAGAGTGTGGCCCTG | 64326 |
rs550095475 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176170071 | TTTATCAGGATAGTA[C/T]AGGAAAATTCAGTCA | 64326 |
rs550099257 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176029683 | GGTTGGAAACCAGTA[C/T]TGGGAATGGAAGCAT | 64326 |
rs550104646 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176147491 | GTATTAATGACAGTA[C/G]AATCACTGTACACTA | 64326 |
rs550121193 | snp | A/C | 0.000886525 | 0.0210351 | intron-variant | RFWD2 | GRCh38.p7 | 1:176165686 | GCTAGACTCCATCTC[A/C]AAATAAATAAATAAA | 64326 |
rs550124260 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176073080 | ATTGGCATTAGGTTT[A/C]TCTTGGACAAGTTAC | 64326 |
rs550141600 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176123695 | AATGTGTAACTTTAC[A/T]GAGTAGAGTAAAAGA | 64326 |
rs550151367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176187811 | AAAAAGAGAAAATAC[A/G]GGAAAATATACATTA | 64326 |
rs550161287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176064702 | TCTGTCGCCCAGGCT[A/G]GGGTTCACTGGTGTG | 64326 |
rs550177137 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176136473 | TAAGGATGTGAGAAA[C/T]TCTTGATTCCTTACT | 64326 |
rs550219593 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176132586 | ATATACTATATATAC[A/G]CACATATACACATAT | 64326 |
rs550237964 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176089818 | TCTGAATAATGTCAC[A/G]ACAAATAAAGAAGGA | 64326 |
rs550242150 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176085662 | TCTGGTAGACTATGT[C/G]AAAAATACATACTTT | 64326 |
rs550244394 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176168063 | AAATTCAATTTACGA[A/T]TTTTTTTTTTTTGAA | 64326 |
rs550245373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176057216 | CTATGTAGCTCCGAA[A/G]TGATTCTAAACATTT | 64326 |
rs550260176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176171750 | AAGTATGCCTGTATA[C/T]ACAATTTTGTTACAG | 64326 |
rs550272823 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175993516 | ATTTAGACGAATGTA[A/T]AACTAGAATAACCAA | 64326 |
rs550292584 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176067676 | TCATTCTCCAAGCCC[A/T]TGTGAGATCCAATTT | 64326 |
rs550303813 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176026001 | CAGCAAATAAATACA[A/T]GAAAGTCTGATAAGA | 64326 |
rs550323204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176096934 | TTACATTTGTGGCCC[A/G]GGGTTCGATCCTGGC | 64326 |
rs550325124 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176057680 | GGCGTGATCTCGGCT[C/G]GCTACAACCTCCACC | 64326 |
rs550329710 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175973753 | ATTTATCTACCCAAT[C/G]AACACTCTAATATTT | 64326 |
rs550336947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175986374 | CTTTAAAACATAAGT[A/G]AAAAGTTTGAGGCAA | 64326 |
rs550346849 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175986320 | CACCGAACCTAGCCT[A/C]AGAATTATTTTTTCA | 64326 |
rs550363945 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176106219 | TATTTTTTGTAGAGA[C/T]GAGGTTTCTCCATGT | 64326 |
rs550371323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176129567 | TACTACATTTATTTA[C/T]TACCTTAGAAAAACA | 64326 |
rs550374816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176050815 | AGAAACTGAGGTATA[C/T]TAATGTTAAGTAATT | 64326 |
rs550380148 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176064413 | TTCAGTAAATTCTGG[A/G]ACCAACTTTTGAATC | 64326 |
rs550382137 | in-del | -/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175973608 | TTTGAAAAATATAAT[-/G]GTTGCCTTGTAAAGC | 64326 |
rs550391844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176081635 | ATATTAAGAAGAGTA[C/T]TGGATGAGTATTTGT | 64326 |
rs550406314 | in-del | -/TT | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176094159 | TAGTCAGCAACACTG[-/TT]TTGTTTTACTTATTT | 64326 |
rs550408664 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207885 | AAGTCAGTGAAGTTT[A/T]CTGCGAATTGCAAAC | 64326 |
rs550415687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176148179 | AACAGTTGAGAATAA[A/G]AAAAATCTAGTCACA | 64326 |
rs550461529 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176068545 | CCATATAAAACACAG[A/G]AAAATTTCAAAGGTC | 64326 |
rs550465420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176104043 | AAACATATCATAAAG[C/T]GTCTACAATAAAGGA | 64326 |
rs550472796 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176113079 | GCCAGCAGTGGGGTT[G/T]TTGGAACATATGACA | 64326 |
rs550473326 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:175973260 | TAGTAAAAGAGTTAA[C/G]TTTGCAAATGGAAAT | 64326 |
rs550481411 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176198334 | GCAGAAATAAACTCA[C/T]ATATATGGTTAATTT | 64326 |
rs550488400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176154366 | CAGCACTATTTACAA[C/T]AGCAAAGACATGGAA | 64326 |
rs550489254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176065253 | TTACTGTGAACAGTA[A/G]ATAGAGAAATTAACT | 64326 |
rs550498803 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176007587 | CTCAGCTGCAGGTCT[C/G]TTGGAATACCCTGCC | 64326 |
rs550506518 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176006970 | GTTCCATTCTCCCCA[A/T]CACTTTCAGGTATAC | 64326 |
rs550525370 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176147723 | AGCTATAAAATCAAA[C/G]TCAATATCACAGATG | 64326 |
rs550528428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176013476 | GATTTAAGTTTCATT[C/T]AATGAGCAAACCTAC | 64326 |
rs550529687 | in-del | -/CTGAGTTAGCACGTTCAT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175988528 | GGCTCTGGAGCCAGA[-/CTGAGTTAGCACGTTCAT]CTGTCGGCCAGGCGT | 64326 |
rs550531904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176204647 | AAATACTCAGGACCA[C/T]GGTGGCTCACACCTG | 64326 |
rs550557701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176205317 | AGCCCAAATGTTCAA[C/T]GAAAAACAGATTAAT | 64326 |
rs550562505 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176173158 | CTACTAAAAATACAA[A/T]AAATTAGCAGGGTGT | 64326 |
rs550579421 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176150636 | TAACAACTTTATACA[A/G]AAAGTAACTCCAAGT | 64326 |
rs550579532 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176143208 | TGAACCCTGGTGACA[A/T]TAAAAACTTAAGACT | 64326 |
rs550590889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176018572 | TTCCTACTCTCAATC[C/T]TTGAGGAACATAAAA | 64326 |
rs550591940 | in-del | -/CTT | 0.0193772 | 0.0965046 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176177291 | TTAAAAAAAACACTC[-/CTT]AAGTATTTTTCACCA | 64326 |
rs550594376 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175980414 | AGTATTTCATCATAT[A/G]ACAAAAAAGTTTTGT | 64326 |
rs550609608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175991861 | GGGTAATGATATGCA[C/T]AGAGATGTCATCTTC | 64326 |
rs550624962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176110218 | TCCTTTGATGCAAAG[C/T]ATATAGGGAGACAAG | 64326 |
rs550629258 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176152214 | GCAGTGAGCAGTGAT[C/T]GCACCATTGCAGTCC | 64326 |
rs550643755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176074712 | GTAAAAAATTCAACA[C/T]TACATTAAATCAAGC | 64326 |
rs550663819 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176180491 | AGGGACACATATCTC[A/G]GGTCCACCTGAGAAA | 64326 |
rs550667658 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176044218 | GTTGTGCCAAATCAT[A/G]TAAGCCAAATAAACT | 64326 |
rs550681169 | in-del | -/CAAA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176118748 | AGAGAGGCCCTGTCT[-/CAAA]CAAACAAACAAACAA | 64326 |
rs550695621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176115435 | AGCCTGGGCAGGAGC[A/G]GGACTCTGTCTCAAA | 64326 |
rs550699310 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176123129 | TTTTAAATTATCAGA[G/T]GATATAGTTGATACA | 64326 |
rs550722998 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176047343 | TATATGTATTATTAT[C/T]ATCTACATTTTACAG | 64326 |
rs550725213 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175966398 | ATTTTATATGGATTA[C/T]TTCACTTAATCTGCA | 64326 |
rs550744381 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176182702 | AGGTCAATTTATGGA[C/T]CAAAGAGAACACTAC | 64326 |
rs550747964 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176095736 | GTGCTTATGTTTGTA[C/T]TTGTGATACAAAAGC | 64326 |
rs550750580 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176058476 | CAACCCTGTGCTCTC[A/T]GAAACATGTGCTGTG | 64326 |
rs550753043 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176014302 | GTGTGTCAAGCACTG[C/T]CTACTCTCATCAATG | 64326 |
rs550795746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175984806 | GAGATCATTTTGGAA[C/T]TTTAAGATTTGACTG | 64326 |
rs550796589 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176001954 | TGACGAGAAGTCATC[A/C]GAAATATTAACATTA | 64326 |
rs550809504 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176121827 | ATGGCTTTTTAGCAA[C/T]ATGTAGATTTTTGGC | 64326 |
rs550811573 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176145390 | AGAAATGCTCATACA[A/G]TGCCTATGCCTGTAG | 64326 |
rs550818519 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176143950 | AAACTGGGTAAAAAT[G/T]TACTACCTTGAGTGA | 64326 |
rs550842175 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176151458 | ACTCTCAGTACTCTA[A/C]AATACAGCAAGTTTT | 64326 |
rs550847392 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176045530 | TTTCCTCATATAATT[A/C]TCTTTTAAAGCCAGT | 64326 |
rs550852718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175958698 | TATAGAAAAAAGAAA[C/T]TGAAAAGACTTTATG | 64326 |
rs550855537 | in-del | -/CAAA | 0.00517822 | 0.0506191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176189529 | AAATAAACTCATTTT[-/CAAA]CAAACACAAATTTAA | 64326 |
rs550864230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176011300 | AACAGCCAAATGTAG[C/T]TAGAACTAATACTGC | 64326 |
rs550879195 | snp | C/T | | | intron-variant, utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175971907 | CCATAGAGAGCCTCC[C/T]GATGTGGCACTCAGG | 64326 |
rs550885484 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176051282 | ATAGCTGCTGAAAAA[A/G]CCAAGATGTTAAAAA | 64326 |
rs550921255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176144851 | CTATACCTCACATTA[C/T]ACACAAAAATAAATC | 64326 |
rs550929797 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176052981 | GAACATTTCACTTCT[A/C]GTCTTTCACTGTTAA | 64326 |
rs550945532 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176007906 | TGCTTTGTTTACCTA[A/G]GCAAGCCTGGGTAAT | 64326 |
rs550950414 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175948266 | AGACATGCCTCCTGT[A/C]GGAAACTGGGCATCT | 64326 |
rs550956921 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176053564 | CAAAGATCTTTTATT[C/T]TGCCCACTTCCACTT | 64326 |
rs550959028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176006086 | CCTGCTGAATTGATC[C/T]CTTTACCATTATGTA | 64326 |
rs550984669 | in-del | -/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176203016 | TAATGTAGATCCTAA[-/C]TATTTTCTATCAAGC | 64326 |
rs551033133 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176014124 | ATTTGCAGAAAGCAT[G/T]CAGAATTTGATTTGA | 64326 |
rs551033382 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:176007582 | GGACCCTCAGCTGCA[A/G]GTCTGTTGGAATACC | 64326 |
rs551036844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175965762 | CCCAGCTAATTTTTG[C/T]ATTTGGAGACGGGGT | 64326 |
rs551039683 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176190176 | TTCAGATTCGGATCT[G/T]TCTGCATTTTGAAAT | 64326 |
rs551044726 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176156867 | TAACAGTAACACACT[C/T]GTCAGCAACTGACAG | 64326 |
rs551045887 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176089987 | AGATTAACTGAGAGT[C/T]CAGCCTAATTAGGAA | 64326 |
rs551051222 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176098784 | CATCAAGTGTTTTAA[A/T]CCTCTAACATATTTA | 64326 |
rs551077329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176108617 | TCATTGCAAGTAATA[A/G]TAATTCCATTTTGGA | 64326 |
rs551088533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176147068 | TACAAATGAAATCAC[A/G]AAGTTAATTTTCAAA | 64326 |
rs551101271 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175971614 | CCGCCACTCTCCAAT[A/C]CCTTGCCCTATGCAT | 64326 |
rs551113664 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176196108 | GAAAATTTGAAGATA[C/G]AGCTAAAGTAGGGAT | 64326 |
rs551117846 | in-del | -/AAAATAT | 0.00398643 | 0.0444671 | intron-variant | RFWD2 | GRCh38.p7 | 1:176023951 | TGCTGTCAAAGACAG[-/AAAATAT]CATCATAAGAAAACT | 64326 |
rs551125449 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175946097 | ACTTGACATGAGAGT[A/G]AGAGAGAGACTGAGA | 64326 |
rs551128285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176177185 | AACTACTCATAGTTA[C/T]TGCTAGAGAACTGTG | 64326 |
rs551130521 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176128994 | CATATCCCTCCCAAG[A/C]ATATATTCTTTCAAT | 64326 |
rs551133651 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176068649 | CATTTTTTTCCAAAC[C/T]ACATGAAACCTTGAA | 64326 |
rs551134755 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | RFWD2 | GRCh38.p7 | 1:176003532 | TGATTTTTGTATAAG[G/T]TGTAAGGAAGGGATC | 64326 |
rs551147085 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176151815 | ATGTAAATAACTAAT[A/G]TAACTGATTTTTAAA | 64326 |
rs551154934 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176081044 | ACTAATAATTGGCAG[G/T]CTACTTCAGAACCCA | 64326 |
rs551158397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176087955 | TTCATGTCCTTTGTA[A/G]CGACATGGATGAAGC | 64326 |
rs551164085 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175946866 | TATTTTGGGCTCTAT[C/G]TACTGAAAGCCCTGT | 64326 |
rs551177521 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175994810 | GGGAGACTTTAACAC[C/G]CCACTGTCAACATTA | 64326 |
rs551177628 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176032612 | AAGCTCACTCAACAT[G/T]ACTTTTGGCATAAGG | 64326 |
rs551178394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176153651 | AGTAGTGAAAGAGGG[C/T]ATCCTTGTCTTGTGT | 64326 |
rs551202205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176105683 | CTTGCCTATGCTATA[A/G]AATATATTAACTAAA | 64326 |
rs551213389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176140785 | CCTAGATCACATTTA[C/T]CTTAACACCATTACA | 64326 |
rs551228823 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176056536 | TGTGTGTAAGACAAA[C/G]AGAGATTGATCTAAT | 64326 |
rs551263144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176000701 | GGTTCTCAACCTGTA[C/T]ATGGTAGAATTTTTA | 64326 |
rs551277018 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175963462 | GTTTTACAGCCAGCC[C/T]GACCTGGGTTCTAAT | 64326 |
rs551296340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176078067 | GCTAAAATGGCAATA[C/T]TGTTCAAAGCAATTT | 64326 |
rs551303166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175958197 | CAATAATATCAATTT[C/T]AAAAAGCTGGGAACA | 64326 |
rs551306688 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176029752 | AGTAACCTGTAGACA[A/G]CAGTGAATAAAATAA | 64326 |
rs551307885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176036273 | GGGGAGGAAATTAAA[C/T]CCAAAGCAAGAAGAA | 64326 |
rs551309548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176042982 | TGCACTGAGCCACAA[C/T]TGTGCCACTGTACTC | 64326 |
rs551325805 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176090309 | AAAATGTATACCAAC[A/C]ACCTTGGGCACATGT | 64326 |
rs551327968 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176039429 | AATCTAAAGTAAGCA[A/C/G]GGAAAAAAAAAACTA | 64326 |
rs551341508 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | RFWD2 | GRCh38.p7 | 1:175997862 | CTCAGGGATCTAGAA[C/G]TAGAAATACCATTTG | 64326 |
rs551344251 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175996119 | AATAAATGTAATCCA[G/T]CATATAAACAGAACC | 64326 |
rs551363238 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176186569 | AAAAAAAGGGCACCT[C/G]AAAGAACTAAGGAAT | 64326 |
rs551364510 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176194714 | CTGGGTACAAGAAAC[A/C]CACTTTAAATATTAA | 64326 |
rs551370603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176147583 | AAGAAAATATGGTCC[A/G]AGAGAAAAGAAAAAA | 64326 |
rs551376835 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176178296 | AATTTAACTCTTTTT[G/T]TAAATCAGCAGCCTG | 64326 |
rs551384596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176180279 | CAGGAAAGCAACATA[C/T]GCCTGTCTGCTGCCT | 64326 |
rs551389256 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176068310 | CAATGGTTCTCAAAG[C/T]GTGGTTGCAGACCAG | 64326 |
rs551405477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176099619 | TTTACATCAGTGCAA[C/T]AAGAATCCATTTTCT | 64326 |
rs551405990 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175996621 | AGACAAACAGAGAGC[C/G]AAATCATGAGTGAAC | 64326 |
rs551407615 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992583 | TAAAAAATGGCGGAC[C/G]AGGAGATTATATCCC | 64326 |
rs551411573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176055671 | AGGCATAGTTAACCC[A/G]TCCAAAATTGAGTTT | 64326 |
rs551424608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176187001 | AGCAGGGGTACAGTA[C/T]GTGTCATGTCACATA | 64326 |
rs551430901 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176036418 | AAACAATAAATAAAC[A/G]AGAGGACACAAAATA | 64326 |
rs551435222 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175954216 | ATGGAAATGAGAAAC[C/G]ATTTTGAACTAAAAG | 64326 |
rs551445130 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176091340 | AACAGAGCGAGACTC[C/T]GTCTCAAAAAAAAAA | 64326 |
rs551445692 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175952485 | TACACAAAATTAAAG[A/T]CAAAATAAAGATATT | 64326 |
rs551451798 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176071397 | TTTATAAATTACCCA[C/G]TCTCGGGTATTTCTT | 64326 |
rs551459950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176179360 | AGGAGAACATTATGG[A/G]TTTTAGCAAATAACT | 64326 |
rs551502800 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176068112 | CTGTACTGTGAACCT[A/C]AAACTGCTCCATAAA | 64326 |
rs551505712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176193289 | GTGTTGACAAGATGT[A/G]GAGAAATTAGAACCC | 64326 |
rs551512145 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175974863 | TATGGGTGGTCAAGG[C/T]TGCAATGAGCCATGG | 64326 |
rs551513548 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175954943 | AAATATATATATATA[A/C]TTCACTATGTAAAGA | 64326 |
rs551549905 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176111299 | TTATTTTTATTTATT[G/T]TTTGTGTGTGTGTGA | 64326 |
rs551553280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176002191 | ACCTCTTTCTCTCTC[C/T]TCATCTTTTGGAAAT | 64326 |
rs551554905 | in-del | -/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176118348 | GTCTACACAGCAGTC[-/T]TTTTTTTTTTAAGGC | 64326 |
rs551569207 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176048442 | GCAATGCAGTAGATT[C/T]ATTTGTACAACCTCA | 64326 |
rs551588150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176175057 | CCTCTCTCAAAAGTT[C/T]TCCTCCATGTATTCC | 64326 |
rs551590088 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176193055 | ATGGATGACAACTTT[C/T]CCTTAACTTCCCTTT | 64326 |
rs551598724 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176012950 | CATTATGTAGTCCCT[A/G]GGTATCCTCGGGGGA | 64326 |
rs551610427 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176004006 | TGTTCTTCCATTTGT[G/T]TGTATCCTCTTTTAT | 64326 |
rs551614798 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992779 | CCACCACAGCTCAAG[A/G]AGGCCTGCCTGCCTC | 64326 |
rs551619123 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176199028 | TGCTGGTAGAAATGC[A/C]AAATGGTGGCCGGGT | 64326 |
rs551644619 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176093825 | CCTAGGTGACAGAGC[A/G]AGAGACTCTGTCTCA | 64326 |
rs551657840 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | RFWD2 | GRCh38.p7 | 1:176117607 | TTTCTACTATAAACA[C/T]GCTTAGGCTAGGCAC | 64326 |
rs551673865 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175998778 | CACATTTTTGGTGTA[C/T]TCAAAAAACATAAGG | 64326 |
rs551685492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176084649 | TTGTTGTTAATTTCA[A/G]ACAAACAAACAAATT | 64326 |
rs551687506 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176091954 | AGAATACTAACTAAA[A/G]GAGAAAAAATAGATT | 64326 |
rs551696147 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176150349 | ATAACTGAATTAATA[C/T]GTTTTACAACTGAAT | 64326 |
rs551705298 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176161040 | TACCTGATGGTCCCA[A/G]TCCCAGGGCCTCTGC | 64326 |
rs551719472 | in-del | -/A | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:175998212 | AACTATCACAAGAAC[-/A]AAAAAACCAAACACC | 64326 |
rs551727615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176124178 | GGTACAAGAGATATT[C/T]TGGTACAGGCATGCA | 64326 |
rs551750852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176124696 | ACAGGTTACTTCCAA[A/G]TCTTGGCTATTGTGA | 64326 |
rs551753240 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176099811 | GACCTGTGATAAGTA[A/G]AGAATGTCACCTTCT | 64326 |
rs551766090 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176080433 | GAGCAAAGATTAATG[A/G]TAACAGAAAACAAAA | 64326 |
rs551772326 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176124877 | GTACTAAATTACATT[A/C]CCACCAGCACCATAC | 64326 |
rs551772745 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175953204 | AAGTTAAACATATTA[C/T]AAACTTTAGAGAAAC | 64326 |
rs551777105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176076400 | AAGAAATTAAGGCAG[A/G]AATAACAAAATTCTT | 64326 |
rs551784637 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RFWD2 | GRCh38.p7 | 1:175994708 | AACTATGCTAAATAT[A/G]TATGCACCCAATACA | 64326 |
rs551808045 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175987962 | TCTCCAAAATTGGAA[A/C]TATTACTAACAGAAC | 64326 |
rs551824094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176028004 | GTCATGTCTTACCTG[A/G]GGGCAGGCAAGAGAG | 64326 |
rs551824523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176035342 | GAAGACAGAACAATA[C/T]AAATTACCCAACCTG | 64326 |
rs551828323 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176177984 | CGGATATGCAAATAT[C/G]TACTGAAAAATGACC | 64326 |
rs551834904 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176173156 | CTCTACTAAAAATAC[A/C]AAAAATTAGCAGGGT | 64326 |
rs551838207 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175959375 | ATCTTTAAAAGCTTT[A/C]CCTTTGGTGAGGAAC | 64326 |
rs551839838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175964173 | GTCTTACAGCTAATA[C/T]TTAATGGTGATAGGA | 64326 |
rs551843587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176086918 | AAACAGAGATACAGA[C/T]CAATCGAACAGAACA | 64326 |
rs551847736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176182474 | GTCACAACCCCAGAG[A/G]TGGGCAGGGGTGGTA | 64326 |
rs551855182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176137714 | CTATTGAAAACAGTA[C/T]CTTATTATTAACTCA | 64326 |
rs551862993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176178902 | ATGCCGGGCTGGGTA[C/T]ATCTGCTAATGCCAG | 64326 |
rs551871220 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175994418 | TTAAAGGTAAATGGA[A/C]TAAATGCTCCAATGA | 64326 |
rs551879418 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176072171 | TTCTGTCACATGTCA[C/T]TGGTAATTCACAAAC | 64326 |
rs551907319 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176024103 | TCTCTACTAGAAATA[A/C]AAAAAATTAGCCAGA | 64326 |
rs551909399 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175949477 | CAGCAGAAAGAGGCA[C/T]TGTGTGGTGCAATAT | 64326 |
rs551912216 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176160139 | TGTGTTTCTTCAATT[A/C]GAAGCCAAAAAGGAA | 64326 |
rs551930441 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176199271 | GCACCAAGCTGAGAT[C/G]GTGCCACTGCACTCC | 64326 |
rs551936255 | snp | A/G | | | intron-variant, downstream-variant-500B, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175968326 | CATTTAAAAAATAAT[A/G]CAGTACTCATAACCA | 64326 |
rs551951211 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176153073 | GGAAGTTGATTCCCT[A/C]ATTCTCCACCATCTA | 64326 |
rs551952205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176040823 | AATAAAGCTTCCAAT[A/G]CTAGAGCTATCCTTG | 64326 |
rs551961319 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176021711 | CTGGGACCCTTTAAC[A/T]CTACTACTGCTGCTT | 64326 |
rs551972766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175956488 | CAAAAAACATGTACA[A/G]TAAAGGAAAAAAAAA | 64326 |
rs551974868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176176075 | AAACTGGTCACAAAA[C/T]AATGACTATTAGTCT | 64326 |
rs551979022 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176102722 | AGGAGGCATGCAGCT[A/G]GAGGCCACAAGATTC | 64326 |
rs551991045 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175966251 | TCCAAGGGGGTTGAG[A/T]GAATTAGCTGTCTGA | 64326 |
rs552021442 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176071039 | TTCTAGATATTGACT[C/G]ACAGAGTTTGGATAT | 64326 |
rs552025543 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176094346 | ACTTGGGTCATCATC[A/G]TATGCCAGTTTAATT | 64326 |
rs552032087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176045310 | ACAGATTCTCAATGA[C/T]GAGTGCCACAAATGA | 64326 |
rs552045694 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175991351 | TTACGTATCTAAATA[A/T]AGAAAAGCTACAGTA | 64326 |
rs552059667 | in-del | -/T | 0.452283 | 0.146906 | intron-variant | RFWD2 | GRCh38.p7 | 1:176084851 | ATAAAATACCAGACT[-/T]TTTTTTTTTCCCCCT | 64326 |
rs552062244 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176071049 | TGACTGACAGAGTTT[A/G]GATATTTGTACCTGC | 64326 |
rs552064706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176196194 | AATGATCTAAGCTTT[C/T]GTACTAAGAAACCAG | 64326 |
rs552067715 | snp | C/G/T | 1.73162e-05 | 0.00294241 | intron-variant | RFWD2 | GRCh38.p7 | 1:176206551 | ATTTAGGGACAAGGA[C/G/T]GGAGTGCTCTTCAAA | 64326 |
rs552089813 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176208859 | CAAGGCGAGTGGATC[A/G]CCTGAGGTCAGGAGT | 64326 |
rs552094027 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176026192 | CAAGAAGGAGAAAAT[C/T]TGATAATATTCATAT | 64326 |
rs552103011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176167080 | TTTGTACTTCAAAAA[C/T]TTAACAGAAGAAAAT | 64326 |
rs552103331 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176006020 | GGACTTGCTTTATGA[G/T]TCTGGGTGCCCTTGT | 64326 |
rs552107909 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176067560 | GCCTGGCCACTGAGC[A/G]GCCCGACTCCAGGGG | 64326 |
rs552112813 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175948807 | ATAAAGACATGTGGG[C/G]ATGGGAATTGTTGAT | 64326 |
rs552113821 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176076567 | ACATGTAGAGGAACT[A/G]GAAGAAAAAGAACAA | 64326 |
rs552114725 | snp | A/T | 1.69e-05 | 0.00290684 | intron-variant | RFWD2 | GRCh38.p7 | 1:176162838 | TAAAGTTCATCATTT[A/T]AAATTTTTTTTAAGT | 64326 |
rs552120290 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | RFWD2 | GRCh38.p7 | 1:176101927 | TTATCCTTATGGCAG[G/T]TAGATATATACTTCT | 64326 |
rs552144313 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176096806 | CTGGTCTGCTTTACA[C/T]AACTTTCTGTATGGT | 64326 |
rs552160619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176038691 | CGTGTGGTGGCGTGC[A/G]CCTGTAATCCCAGCT | 64326 |
rs552160641 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176084714 | TTTGTAAATCTAATA[C/T]ATTTTTTCCTATACC | 64326 |
rs552160676 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176031122 | CCCTGCCAACAATCT[A/T]ATTTTGGGCTTCTGG | 64326 |
rs552188243 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176202908 | CACAGTTAAAAGCCA[C/T]TCTTCGAATTAAATC | 64326 |
rs552202580 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175949227 | ACTCACTATTAGAAT[A/T]AACTTTGGAATATTA | 64326 |
rs552207224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176000147 | TTTTTGCTTTGGCTG[C/T]TTGTGGGATATTACT | 64326 |
rs552222402 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176074490 | TTGGTGTAATTAATA[A/G]AAAAAAAACGAATGT | 64326 |
rs552228888 | snp | C/T | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176162224 | GTATGTGTTACTCAC[C/T]CACTTACTGTCTCAA | 64326 |
rs552231608 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176044655 | AATTTAGGTAGACTT[G/T]AGTTCAAATTCCAGA | 64326 |
rs552251563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176169137 | CAACTTAATTAATAT[A/G]AACAAGGTTTCTCAA | 64326 |
rs552254465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176134282 | GATTTAACAAATCAA[A/G]AACAAATGATTTCAT | 64326 |
rs552254982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175975980 | TTGTTTTGCTATCAA[C/T]GACATTTCATGCTTT | 64326 |
rs552269107 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176201742 | GATGCCCCACCATCT[G/T]ATAGTCCACAGGTCT | 64326 |
rs552286223 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176064766 | TCAATCGATGCCCCT[C/G]CCTCAGCCTCCTGGG | 64326 |
rs552316492 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176107124 | ATAAATGGTTTGATT[A/C]CTGGGAGTCCTTCAG | 64326 |
rs552320912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176188476 | AGAAAAACAATCCAT[C/T]CAGGACCTCTGTAAC | 64326 |
rs552326216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176203918 | ACCAGGGGAGCATAT[A/G]CAAATTACACCACCC | 64326 |
rs552345743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176038126 | TTAAATATCAACTGT[A/G]TTTCTATAAACTAGT | 64326 |
rs552348438 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176017610 | GCTCACTAAAACCTC[C/T]GCCTCCTGGGTTCAA | 64326 |
rs552380193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176182089 | TTCCACTTCACAACA[C/T]AGTGAAAAAAGGTCA | 64326 |
rs552386032 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176071983 | TAGGGTAGAAGTTAT[A/G]AGGGTGGGAATACAT | 64326 |
rs552394183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175983187 | AGAAACTGATGGCTT[A/G]AAGGAATGAAAAAGA | 64326 |
rs552401133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176157798 | GCAGAAAAATATATC[C/T]TACAATAAGGGAAAA | 64326 |
rs552408802 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176057753 | GCCTCTGCCCGGCTG[A/C]CACCCCATCTGGGAA | 64326 |
rs552411931 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176181319 | CCAGCCAGAATTTAC[A/G]TTACTAGAAAGTTGA | 64326 |
rs552420216 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176059705 | TCAGGCCGGTCTCGA[A/T]CTCCTGACCTCGTGA | 64326 |
rs552422531 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176022606 | AAGATGACTGAATAT[C/T]GGTCAGTTTTCTAGT | 64326 |
rs552430796 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176159474 | TCAAATATTTAATAA[C/G]ATTAAAATGTGCACA | 64326 |
rs552443370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176073788 | GCAAAGGAAGAAAAA[C/T]ACGTTTCTGGTTCGG | 64326 |
rs552448730 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175984958 | GCTGATGATTTTACA[G/T]ACTCATAGGCAGAAG | 64326 |
rs552453562 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176075510 | ACAAAGTAGCAATTT[G/T]ATTATACCAAGGAAT | 64326 |
rs552495105 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176058114 | CGCCCGGCCAGCCAC[C/G]CCGTCGGGAGGGAGG | 64326 |
rs552502408 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176018778 | TTGGGAGGCTGAGGC[A/G]GGAGAATCACTTGAG | 64326 |
rs552529879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176183815 | TACAACACTGAAGAC[A/G]TTATGCTAAGTGAAA | 64326 |
rs552541205 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176023274 | CTAGCAAATGTTTAG[C/T]TACACCTACCAAAAA | 64326 |
rs552541577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175999588 | GGAATGCAGATAGCT[C/T]TTTCATATAGAAGTT | 64326 |
rs552573980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175983629 | TGGAACTGGTTAACA[A/G]GCAGAGGTTGGAACA | 64326 |
rs552589360 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176184443 | CTAAATCTAAACATT[G/T]GACAGAAATTATGCG | 64326 |
rs552594211 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207549 | TCTCGAAAAGCGACT[A/G]CGCAGGCGCGCGCCG | 64326 |
rs552602612 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176126108 | ATCATTTCGTTCTAA[C/T]AGTTTTTTGGTGGAG | 64326 |
rs552611512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176016069 | TTTGCAAAAGAAAAA[C/T]TGAGTTCTGGATGTT | 64326 |
rs552616902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176100580 | AACAAAAGGGATGGG[C/T]AATGTAGAAATCTGG | 64326 |
rs552631938 | snp | A/C | 0.227369 | 0.248974 | intron-variant | RFWD2 | GRCh38.p7 | 1:176078630 | TTGCAAAAAAAAAAA[A/C]AAAAATTGACAAGTG | 64326 |
rs552640569 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176120129 | ATATAAGACAGAATC[A/T]TATATTTTTCAAATA | 64326 |
rs552646746 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176060426 | AAAATATATTTTTGT[C/T]CCCAAAGTTACTACG | 64326 |
rs552662847 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175972431 | CATACCATCTGAGGC[C/T]CAGAGAGCAGCAATA | 64326 |
rs552671928 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176075079 | TCTCCTGAATCCAAG[G/T]AACACGTCTGGCCTG | 64326 |
rs552671973 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176191114 | TGCCTTTTTACATGC[A/T]TTATATACTCTAAAC | 64326 |
rs552675324 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176030361 | CTCTAACAGCCTAGG[C/G]CCAAAGGTAATTCAC | 64326 |
rs552678780 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176130563 | AAATTCAACTGATAT[-/A]TTTTTTTAAAAAACA | 64326 |
rs552683883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176054203 | CTCACTCTGTCACCC[A/G]GGCTGGGGTGCAGTG | 64326 |
rs552717942 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176052289 | CTACATGTCTAAGTA[C/T]ACTCCATGATGTTTG | 64326 |
rs552718260 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176178986 | ATTTTTTTTTTTTAG[A/T]TTTTTTTTTTAAAAA | 64326 |
rs552721338 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207918 | TGTAGCAAGTGTTAC[A/C]AATTTTATTAGTTCG | 64326 |
rs552725437 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:175989937 | TATTTCTGCACTCCG[A/G]TAAGATCACTCATTT | 64326 |
rs552727070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176096974 | GAGTCCTTTTTGGTT[C/T]GATACCTGTGCAACC | 64326 |
rs552754399 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176108416 | AATACCAGTATACAA[A/T]CTTTACATAGTACTT | 64326 |
rs552778366 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176038018 | TCTATTTGCAGATGA[C/T]GTAATTGGCTATGTA | 64326 |
rs552783710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176005137 | TTTCTAGTTTATTTG[C/T]GTAGAGGTGTTTGTA | 64326 |
rs552793520 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176082624 | CCAGCCTGACTAACA[A/T]GGAGAAACCCTGTCT | 64326 |
rs552806728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176197680 | CCAATCAAATAAATC[C/T]ATTAACGTACGTTCT | 64326 |
rs552819658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176142060 | AGCTGAGAAGAAAAC[A/G]GAAAAAGCAAGAACA | 64326 |
rs552824545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176156122 | AAAAGTTTGGTGAGA[C/T]TTATAACATGGTTTG | 64326 |
rs552846813 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175990016 | AATTTCTACTCTAAC[C/T]TTTATTATTTCCTTC | 64326 |
rs552851817 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176023461 | TGGTGGCTCACGCCT[A/G]TAATCCCAGCACTTT | 64326 |
rs552859606 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176148920 | AAAATATTTAAAGAA[A/T]TTTTTTAGCCTGAAA | 64326 |
rs552863277 | snp | A/G | 1.67654e-05 | 0.00289524 | intron-variant | RFWD2 | GRCh38.p7 | 1:176043868 | AAAATAAATAACAAT[A/G]GGATAAAAATAATTT | 64326 |
rs552868237 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175995659 | TAGAACAAATGGATA[A/C]ATTCCTCGACACATA | 64326 |
rs552871558 | snp | A/G | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176185527 | ATTATTCTGGCCAGT[A/G]AAATATAGACATCAG | 64326 |
rs552897681 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175973325 | GGAAACTCAGGACTG[C/G]GTTGCTACCTAAACT | 64326 |
rs552914949 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176031464 | AAGAATTTCATTTAA[C/T]TTCCAAAATTTAAAT | 64326 |
rs552917982 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176107909 | ACTGAGGGAAATCCT[A/C]TAAATAACTTACACT | 64326 |
rs552918615 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:176018516 | TAGGAATCAGAACCC[-/T]TTTTTACTCTTTTTT | 64326 |
rs552923282 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176172707 | ATGCCGTCTTAAGCT[A/G]AAGCAATGAAAATAA | 64326 |
rs552928526 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176096462 | AACGACCACACAGGG[C/T]GGGAATGAGCCACAG | 64326 |
rs552931888 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176141514 | TCAAAAAATACATAC[A/G]TACATACATACAGCA | 64326 |
rs552966301 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176001984 | AATCTTAATGAGGAT[A/C]CCTGGTACTTGCTGA | 64326 |
rs552984519 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176047533 | GTGTAAAGGCTAAAG[G/T]TTTAAAGGTTTAAAA | 64326 |
rs552995176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176040516 | AGAGACAGGGTCTCA[C/T]GCAGGCTGGTCTCAA | 64326 |
rs552998094 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176043408 | ACAAATGAAAAGCAA[A/G]TAAGATGTTGATATA | 64326 |
rs553001603 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176011370 | ATGAATAATCTACAA[A/G]TATGTATGGTGTAGT | 64326 |
rs553010711 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176134706 | TTCTCAAATTTAGAT[G/T]TTTGAATGTCATCTG | 64326 |
rs553012998 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175965194 | GGAGGTCATGGACTC[C/T]GTGTATAGTCAAATC | 64326 |
rs553013422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176089034 | TAGGCCGGGCGTGGT[A/G]GCTCACGCCTGTAAT | 64326 |
rs553016062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176006696 | CTCTCTTCTGGCTTG[C/T]AGGGTTTCTGCCGAG | 64326 |
rs553023804 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176203066 | TTCTCGGCCGGGCGC[C/G]GTGGCTCACGCCTGT | 64326 |
rs553028161 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176136216 | TTTTAAGTTATGATG[C/G]CACTCCAAGAAAACT | 64326 |
rs553038928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176102971 | CCCACCAAATTATCC[C/T]AAAAATCTCTGATCC | 64326 |
rs553055879 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176038528 | ATGGTACAAGTAAAA[G/T]AAGAGATAGGGCTGG | 64326 |
rs553076462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RFWD2 | GRCh38.p7 | 1:175967303 | TGGCGTGAGCCACCG[C/T]GCCGTTGAAAGCTCA | 64326 |
rs553089631 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176069370 | ATTTCAAATGTGTCC[A/T]GGAAACTAGAAGCCA | 64326 |
rs553094156 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176011312 | TAGCTAGAACTAATA[C/T]TGCAGTTCTATTTGA | 64326 |
rs553102892 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176165201 | ACTATCATTAAAATA[G/T]ATTTACAAAGTATAC | 64326 |
rs553104667 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176075625 | CTTTAAAATACTTAA[C/G]CATATACACACCCAA | 64326 |
rs553104775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176157523 | AGCCAGAGTAGAAAA[A/G]CCAAGAAATATACAT | 64326 |
rs553113945 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176094816 | TACACATATAACTAC[G/T]TTAATTCCCAATAAA | 64326 |
rs553114676 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176123672 | GTATTTCAAAGACAT[C/T]ACAGAAGAATGTGTA | 64326 |
rs553128617 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176199611 | AAAAGAAAAAAAACA[A/G]TACACTCAACATCAT | 64326 |
rs553133196 | snp | C/T | | | utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175944977 | GCTGGGTATTCCCAA[C/T]GTCCCAAAGGTCATA | 64326 |
rs553138708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176010640 | TTGTTCCAATGGTGA[C/T]GCCAAATTTGATTAC | 64326 |
rs553150576 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176094533 | AATACGACACAAATC[A/G]AACAGAAATATTTAT | 64326 |
rs553155214 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176040447 | CCCAGTTTCCCAAGC[A/G]CTGAGACTACCTGTG | 64326 |
rs553163513 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176166112 | TAACTAAAGATCAAG[C/G]CTGTATTTATTTATT | 64326 |
rs553166005 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176074069 | GTAGCTGGGATTACA[A/G]GCATACGCCACCATG | 64326 |
rs553166216 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176158107 | GGGGGAAAAAAAAAA[A/C]CTCTACTGCAAGGCA | 64326 |
rs553168358 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175948613 | CAAACTCATACATTT[C/T]CATTTTTAAATTTTC | 64326 |
rs553170875 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176125537 | AACGAGTTCACTGTA[A/G]GTGTGTGGATTTGTT | 64326 |
rs553171489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176033902 | TTTAAAATATTCTCT[A/G]ACTATAAAGTTATCA | 64326 |
rs553190929 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176177727 | GAGCTTTGTAAACTG[-/A]AGTTGATTTTTATAT | 64326 |
rs553196167 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175995248 | CACATTCAAAGCAGT[C/G]TGTAGAGGGAAATTT | 64326 |
rs553208077 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175983810 | TAGAGCAAAGAAGAC[C/T]CTTGTTATGTTTTAG | 64326 |
rs553224797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176040025 | AAACCTTCATGACAC[C/T]GGATTTGGCAATGAT | 64326 |
rs553240016 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:175999476 | ATAGTACTCCATTTT[C/G]TATATGTACCACATT | 64326 |
rs553250395 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176025533 | AATGGTAACATATAT[A/T]GGAAAAAAAATTGAC | 64326 |
rs553260567 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176074810 | AAAAAAAAAAAAGAT[G/T]ATTACTCTTTGTATA | 64326 |
rs553267105 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176137107 | ATCCCCTCACCCAAA[A/G]GCAACCACAAGTCAG | 64326 |
rs553270952 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176115564 | CCTTCCTGGCTAACA[A/T]GGTGAAACCCCGTTT | 64326 |
rs553284049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175949121 | TGAGCAAAGATTGCA[C/T]CACTGCACTCCAGCC | 64326 |
rs553300532 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176176854 | AATGTCATAGTTAAA[C/G]AGTATATGTGGATAT | 64326 |
rs553307569 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176099845 | GGCCCAGAGCTCCAA[C/G]TTTATTTTGAGACGT | 64326 |
rs553314960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176128193 | TCTAACACAGTGTTT[C/T]ATACACGCTGGCTCA | 64326 |
rs553342055 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176179818 | TTTCTTTAGTATCCT[A/C]ATCTTATTCCACATC | 64326 |
rs553374617 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176050504 | ATAAAGTAAGAGCAG[C/T]TGTCAAAGGTCTCAT | 64326 |
rs553379694 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176171247 | TTTGCTACAGCTTCT[A/C]CATCAGCACTTGCTG | 64326 |
rs553409824 | in-del | -/AAGG | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:176151271 | AGAGAAAGAAAGAAA[-/AAGG]AAGGAAGGAAGGAAG | 64326 |
rs553411020 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176097821 | TTGCAGTGAGTCGAG[A/T]TCATGCCACTGCACT | 64326 |
rs553425089 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176045047 | GCAGGAAATGTTTAA[C/G]GGCACAGACTCTAGA | 64326 |
rs553434689 | in-del | -/AAGG | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175964392 | AACAACTTCATGACA[-/AAGG]AAGGTAAGTTCCTTG | 64326 |
rs553448501 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176080690 | AAATGTCTTAAAAGA[C/T]ACAAACTAATTATAA | 64326 |
rs553452440 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176035683 | TCAGACTTTAACATT[G/T]CTGTCTCATAATCAA | 64326 |
rs553455513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176173888 | AGCAACCAGAGAGAC[C/T]GCGGCAGGAGAATCC | 64326 |
rs553475681 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175993030 | TCACACCGCCGGGTA[C/T]TCCTCTGAGACAAAA | 64326 |
rs553478611 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176019575 | ATCAAAACATCACTA[A/C]CAGGGCCTGGCACGG | 64326 |
rs553479066 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176182136 | CCTTTTTTAAAAAAT[A/G]CCACAATGGATATGT | 64326 |
rs553481611 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175964789 | GCTGAATTTAAATAT[A/C]CTTCCTTAAGTAAAT | 64326 |
rs553484433 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176018125 | CTGAATAAAACCTTA[A/C]AGATGCACTAATGTT | 64326 |
rs553505557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176162283 | GGTAGTATTTGCTTA[C/T]GCTAAGGTGTGTGTT | 64326 |
rs553505643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176022723 | GATGCCTTGCTGATA[C/T]TATCCCCTGCTTCAG | 64326 |
rs553516890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176168216 | GTGCGCACCACCACA[C/T]TTGGCTAATTTTTTG | 64326 |
rs553517013 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175974405 | TGTGATAGTAAGTCA[A/G]TGCAATAGACTACAT | 64326 |
rs553522414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176087138 | GACTTAAATGTTAGA[C/T]CTAAAACCATAAAAA | 64326 |
rs553525912 | in-del | -/TA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176127593 | GTGTGTGTGTGTATG[-/TA]TGTATATATGTGTGT | 64326 |
rs553556230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175978991 | GGGATCAGCAAAATC[C/T]AACAGACATTAGGTA | 64326 |
rs553561504 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175997590 | AAAAGTGGGCGAAGG[A/G]AATGAACAGACACTT | 64326 |
rs553601078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176122009 | GCCGGGCATGGTGGC[A/G]GGCGCCTGTAGTCCC | 64326 |
rs553617275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176074181 | ATCTGCCTGCCTCGG[C/T]CCCGCAAAGTGCTGG | 64326 |
rs553619922 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176125772 | TGAAGAATGTCATTG[G/T]TGTTTTGATAGTGAT | 64326 |
rs553633587 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175985888 | ATTAAAGTGAAACTA[A/T]ACCTGAAACTTGGAT | 64326 |
rs553658670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176063938 | ATAGCCACTCATCAC[A/G]AATAGATCAGAAAAT | 64326 |
rs553694047 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176029812 | TATGAAACGGGATTA[C/T]GTAAGAATTTAATAT | 64326 |
rs553694771 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176036352 | CAACAAAACCAAAAG[C/T]TGAGCATTTGAAAAG | 64326 |
rs553716806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175997929 | ACTATAAATAATGCT[A/G]CTATAAAGACACATG | 64326 |
rs553739463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175946290 | AAAAAGGAGACTACC[A/G]TGTAAATTAGTGCAG | 64326 |
rs553744932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176110960 | GGATCGAGACCATCC[C/T]GGCCAACATGGTGAA | 64326 |
rs553749276 | snp | C/T | 5.31967e-05 | 0.00515708 | missense, utr-variant-5-prime, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176206657 | GCTTCCTGCTGCCGC[C/T]GCCTAGGCTGGAGCT | 64326 |
rs553762968 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176106771 | ATTTGAGTAACAGCA[A/C]AGCGGCTCTGCATGA | 64326 |
rs553768231 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175993399 | GCTGGATGGAGAATG[G/T]CTTTGACGAGTTGAG | 64326 |
rs553781984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176111344 | CTGTTGCCAGGCTGG[A/G]GTGCAATGGCATGAT | 64326 |
rs553802292 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992603 | GATTATATCCCGCAC[C/G]TGGCTCGGAGGGTCC | 64326 |
rs553802437 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175986739 | TATGGGTCACAGAGG[C/G]ACATTATGACACCAT | 64326 |
rs553832559 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176020268 | GTGAGCCAAGATCAC[A/G]CCATTGCCCTCCAGC | 64326 |
rs553851695 | in-del | -/ACA | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176197199 | TGACAAAGCTATGAC[-/ACA]ACAACAAGTGGCCCA | 64326 |
rs553861565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175987527 | GGTAAAAGAAAGTGG[C/T]AACACTTACACAGGC | 64326 |
rs553885960 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176205731 | GACTAACCTCTCTAT[A/C]CCAAATGTCATGACT | 64326 |
rs553895106 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176012680 | GTACCATTTTTTTTT[A/T]AACCTTATATTGTAT | 64326 |
rs553904861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175981105 | AAAAAGATAAGACTT[C/T]CATCTGGAATCTTTT | 64326 |
rs553907734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176180391 | CTTGACCATTACCAG[C/T]CTGCATACAAAGCTT | 64326 |
rs553935018 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176007603 | TTGGAATACCCTGCC[A/G]TGTGAGATGTCAGTG | 64326 |
rs553938607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176129250 | CCTACACTTTGATTC[A/G]TCTGGAACTTTGTCA | 64326 |
rs553945543 | snp | A/G | 0.089084 | 0.191327 | intron-variant | RFWD2 | GRCh38.p7 | 1:176002980 | TCCCACCAACAGTGT[A/G]AAAGTGTTCCTATTT | 64326 |
rs553946042 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176124394 | TTTTATCCATTAAAC[A/G]TTCCCACCTCCCCTG | 64326 |
rs553948078 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | RFWD2 | GRCh38.p7 | 1:176163422 | GACAAAGTCTCGCTA[A/T]GTTGCCCAAGCTAGT | 64326 |
rs553948441 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175961996 | GAAAATATGAGGTGG[G/T]GTAAGCATGTAAACT | 64326 |
rs553958239 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175999959 | AAATGGATTATTAGA[-/T]TTTTTTTCCCTACAA | 64326 |
rs553969341 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:175995388 | GAAGGCAAAAAATAA[C/T]TAAAATCAGAGCAGA | 64326 |
rs553979175 | in-del | -/CCTCTC | 0.00517822 | 0.0506191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176057312 | ACTTCAAGAATGTGA[-/CCTCTC]CCTCTCCCTCTCCCT | 64326 |
rs553997579 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175949611 | GAAAATCTCACTGAT[C/T]AACCTAGTTGCCATT | 64326 |
rs554005718 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176106220 | ATTTTTTGTAGAGAC[A/G]AGGTTTCTCCATGTC | 64326 |
rs554005959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176201119 | GCTCACTGGAGCATT[C/T]TGGATTTCAGATTTT | 64326 |
rs554030962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175981941 | CCACAATGAGGTATC[A/G]CCTCACAACTGCTAG | 64326 |
rs554036595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175983289 | CCAGTGGGAGGTAAA[C/T]GACTCATGGGGGCAA | 64326 |
rs554037675 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175999759 | CCTTTTCTCCACATC[C/T]TCACCAGCATTTGTT | 64326 |
rs554041450 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176119645 | TTATACATTCATACA[C/G]ACACACACACACACA | 64326 |
rs554060458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175988773 | GGGGGGCAGATGCTG[C/T]AGTGAGCGGAGATCA | 64326 |
rs554080925 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207347 | GGGGCTGCGCTCAGA[C/T]GCTCAGGGCGCGCCC | 64326 |
rs554088303 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176082071 | TACCTGAGAATACAA[C/T]GAATCTATTCTCCAG | 64326 |
rs554091267 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176078114 | CCTTAAAATACCAAC[A/G]TCATTTTTCACAGAA | 64326 |
rs554103076 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176130466 | AATTTAAAACAGATT[-/A]AAAAAGGTTCTAAGT | 64326 |
rs554115691 | in-del | -/A | 0.00597247 | 0.0543191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176045773 | GCAGAATATTCTTGT[-/A]AAAAAAATTCTTAAA | 64326 |
rs554123132 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176194630 | CGACAGAGCAAGACT[C/G]TGTCTCAAACAACAA | 64326 |
rs554124558 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176203897 | GGAGAAGGACAGGTC[C/T]CTATCACCAGGGGAG | 64326 |
rs554137372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176198888 | GATAAAACTACATAT[C/T]CACAAAAATGACTAA | 64326 |
rs554139591 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | RFWD2 | GRCh38.p7 | 1:175995128 | ATGGAAAGTGAACAA[C/T]TTGCTCCTGAATGAC | 64326 |
rs554141120 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176203401 | ATGCAAACGTATACT[G/T]CTGCTGCAAGAATGG | 64326 |
rs554151894 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176020939 | GGGCAAAAATTACTG[A/T]TATTACATTTTGCCT | 64326 |
rs554177847 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176108718 | TTTATTTATTTGCAA[A/T]AATTGAGTATTATTT | 64326 |
rs554178023 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175977929 | AATATCCAATATTCA[C/G]TTTCCTTCTTTCTAC | 64326 |
rs554191629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176192820 | CAGGGGTGAAAGAAA[C/T]CTCCAAAATGCATGG | 64326 |
rs554201888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176146250 | AACACCCTTTTGTTT[A/G]ATCTGACCATGAAGG | 64326 |
rs554204339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175984083 | GCTGCAGAAATTTGC[A/G]TAAGTAACATGGAGC | 64326 |
rs554208858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176116200 | CTGGACAACACGGTG[A/G]AATCCATCTAGATCT | 64326 |
rs554217606 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176152622 | CCAGCTAATTTTTGT[A/T]TTTTTAGTAGAAACT | 64326 |
rs554220051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176062176 | TGGATAATTTTTTTT[A/G]TGTTTTTAGTAGAGA | 64326 |
rs554224055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176160189 | TATGAGAAGGTAGGA[A/G]GAAGGTTACCAGTTC | 64326 |
rs554229725 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176024906 | TACACTGAAAATTAC[A/G]AAACTATTGATGATA | 64326 |
rs554243351 | in-del | -/AT | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176059853 | AATCTGAATTTTCAC[-/AT]GTCACAAAGTATTAT | 64326 |
rs554255536 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176073576 | ATTATTGCTGTGTGT[-/A]AAAAGAATGCAATTA | 64326 |
rs554263360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176114602 | GCGGGGGGAGGGAGT[A/G]GGGGGGAAAGGGTCT | 64326 |
rs554280529 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176019618 | GCAATCCCAGGACCA[A/T]GGGAAGCATAGGCAG | 64326 |
rs554281442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176017744 | TGGCCAGGCTGGGCT[C/T]GAACTCCTAACCTCA | 64326 |
rs554287142 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176034839 | CCACAGCAAAAGCTC[C/T]GAGAAATGAACTGAT | 64326 |
rs554289077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176026430 | ACAGCTCTACCTCTA[C/T]GTTACAGATAAAAAA | 64326 |
rs554289589 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176075421 | AGCAATATTTGACAC[A/G]TTAAAACTTACCAAA | 64326 |
rs554299544 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176193441 | CAGAGACTAGAAACA[A/T]GTGTTAAAACAAAAA | 64326 |
rs554333039 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176005723 | TATGAGAGATAGTTT[G/T]TTATAATCTCTGTTC | 64326 |
rs554339446 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176181910 | AACATAAAAATGAAA[C/T]TGTATTATAATAAGG | 64326 |
rs554348717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176027294 | ACCTTATGTTTGTGA[A/G]TAAGTAATAAGCATT | 64326 |
rs554371023 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176030181 | ATTTGATTTGTTCCA[C/T]GTTATTCTCCAATAA | 64326 |
rs554376589 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176098956 | TCAATCTTCTTTAGG[A/T]TATATTTTGGTGACT | 64326 |
rs554381380 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176097296 | ACACATGAGAAGGAA[A/G]AGACCTCTGTTTTCC | 64326 |
rs554384313 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176096277 | CCTCTTCTTTTTTTT[G/T]CAGGACAGTAACAGC | 64326 |
rs554391509 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176185997 | AAATATGTATAGATG[A/G]TATTACAACACAATG | 64326 |
rs554404589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176196255 | AAGAAATTTATAAAG[C/T]AAACTGAAAATTAGT | 64326 |
rs554405306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176191992 | GTGCTAGCTTCAGGG[C/T]CAGAAGTTCGAAAAG | 64326 |
rs554428479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176049228 | TGATGACCTAAATAT[A/G]TCTATTATTTCTTCT | 64326 |
rs554434828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175965467 | TTGATTTCCTGACAC[A/G]CAGAATCATTCTTTT | 64326 |
rs554443961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176145748 | AAAGATTACATACTG[C/T]ACAAGCACACTTAAA | 64326 |
rs554446249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176063142 | TCGGCTCACTGCAAG[C/T]TCCGCTTCCTGGGTT | 64326 |
rs554459758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176102140 | CTCAGGAAGTTTGTG[C/T]CATTTGCAGCGGGGA | 64326 |
rs554462537 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176048862 | GAGAAAACTGACACA[G/T]AAGTAAAAATGCTGT | 64326 |
rs554471142 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176166109 | TATTAACTAAAGATC[A/G]AGCCTGTATTTATTT | 64326 |
rs554472248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176005345 | GTTTTTTGTGTCTCT[A/G]TTTCCTTCAGTTCTG | 64326 |
rs554474937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176013616 | GTTTACAAAGACTAC[A/G]AATGTATTTCAACTC | 64326 |
rs554486269 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176144209 | TACATAGAAAACATA[C/G]AAGAATCTACAAATA | 64326 |
rs554502039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176153220 | GCAGCAAAGCAGGTA[A/G]GCTTGTCACTTATCT | 64326 |
rs554503709 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176055220 | AGGTGGATAACCTGA[C/G]GTCAGGACTTTGAGA | 64326 |
rs554505444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176017238 | CAGTCTAGACTGTGT[A/G]CCAAAAAGCAATAAG | 64326 |
rs554509056 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175963113 | TAAATTATTTAATAA[A/C]CTACCTGAGTAGACT | 64326 |
rs554511982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RFWD2 | GRCh38.p7 | 1:175967399 | GCTGAGGCATGAGAA[C/T]TGCTTGAACCCAGGA | 64326 |
rs554524910 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176188962 | TTAGGAAAAAATATG[C/T]AGAGACAGTAACTGA | 64326 |
rs554525503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176181137 | CAGTGGGTTCTCAAG[C/T]GGGAATAAATAAAGT | 64326 |
rs554537269 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176128529 | CTCACAAGAATAAAA[C/G]AATCAAATGGTTTTA | 64326 |
rs554568863 | snp | C/G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176043414 | GAAAAGCAAATAAGA[C/G/T]GTTGATATAAAGTAC | 64326 |
rs554573513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176156435 | GTGTAGACTCAAACC[A/G]AACTATATCAATAAT | 64326 |
rs554600506 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176157356 | AATCAATTTCAAAGG[A/C]CTAAACACATGCAAA | 64326 |
rs554612141 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176157204 | ATCTCAAAAAAATAA[C/T]AACAACAACAATAAT | 64326 |
rs554634637 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175970237 | AGAAACCAGAAACCA[A/G]GGAGATAAAATGGTT | 64326 |
rs554643975 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176196699 | AACACCAATTTCATA[A/C]AAACTCTTTCAGAAA | 64326 |
rs554644238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176164049 | TTTATTTTATTTCAA[A/G]TTAGAAAACAGTTTT | 64326 |
rs554657119 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176008657 | TTTACTGAAAAGCAG[A/G]CACTTTGGAAAATAC | 64326 |
rs554682106 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176031322 | TCTTTTGGAGGAAGC[A/G]TAGAAGAAATCAAGT | 64326 |
rs554691876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176043363 | ATCAATTTATTGTTA[C/T]GGGGAGAGGGAAAGA | 64326 |
rs554713476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176176110 | TTCCTCATTTTCAAC[A/G]TAACTAATCTAATAA | 64326 |
rs554720627 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175946200 | AAACACTGATCAGTT[-/A]AAAAAACCTCGTTTT | 64326 |
rs554728689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176194453 | GACCATCCTGGCCAA[C/T]ATGGTGAAACCCCAT | 64326 |
rs554743549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176024159 | AGCTTCTCAGGAGGG[C/T]GAGGCACGAGAATCA | 64326 |
rs554744354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176072693 | TACAATAAGGAACAT[A/G]TTAAAAGTTACCCTC | 64326 |
rs554746436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176154475 | AAAAAAGGAGATCAC[A/G]TCCTCTGCAGGAACA | 64326 |
rs554750462 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176208222 | GGTCGGATCACCTGA[G/T]CCTGGAGGTGAGGAT | 64326 |
rs554757655 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176081999 | GTAAAGTCCACTTCA[A/G]TAAACTATTGGAAGA | 64326 |
rs554759657 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176147925 | CTTTTTTTGGGACAG[A/G]TTCTCGCCCTGTTGC | 64326 |
rs554774158 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175994441 | TCCAATGAAAAGACA[C/T]AGACTGGCAAACTGG | 64326 |
rs554788009 | in-del | -/T | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176136904 | AATTCAGCATGTCAG[-/T]TGTTAATCACACTTT | 64326 |
rs554817382 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176050038 | TAATAATTAAAACAA[C/G]AGATTTATAAAAATT | 64326 |
rs554822020 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175955621 | CACTAGAATAAATAA[A/G]TTGTCTTCAGCAAGA | 64326 |
rs554823765 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175963623 | TATACTGCCTGGTTG[C/G]TACTTAATAGATGTG | 64326 |
rs554829109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176038332 | TCCCAAATTGATCTA[C/T]AGATTGAATACAATG | 64326 |
rs554829466 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176045847 | GAAAAATTCCTGATG[C/T]TCAAATACTATTCAT | 64326 |
rs554831066 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176087006 | AAAAACAAGAAATGG[A/G]GAAAGGATTCCCTAT | 64326 |
rs554833257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176169655 | TGACCATCTGAGCCT[C/T]TGGCAAGTCATAATC | 64326 |
rs554847976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176176894 | CAACTACTGTTACAG[A/G]AAATGTTAACCAGCA | 64326 |
rs554851608 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176120489 | GGGAAAAAAATTTCA[C/G]GGTAGTAACTAAAAC | 64326 |
rs554852226 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176182149 | ATGCCACAATGGATA[C/T]GTAAGTTACAGGACA | 64326 |
rs554852320 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176175564 | CCCACTGATCTGACA[A/G]GAGACAGAGCACAGG | 64326 |
rs554863093 | snp | A/T | | | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176208357 | TCCCAGCTACTCGGG[A/T]GGCTGACATGGGAGG | 64326 |
rs554873154 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176189508 | AATATCTTTCAAAAT[C/G]AAAGCAAATAAACTC | 64326 |
rs554877674 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175970226 | CAATAGCTGTGAGAA[A/G]CCAGAAACCAAGGAG | 64326 |
rs554879693 | in-del | -/AT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176126265 | ACTACGTTGAGTAAC[-/AT]TGGTGAAAGTGGGCA | 64326 |
rs554880229 | snp | A/G | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:175948915 | CACACCTGTAATCCC[A/G]GCACTTTGGGAGGCA | 64326 |
rs554881591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176143420 | TCTCCAGTAAGATCT[C/T]TAAACATTCAAAAAA | 64326 |
rs554884184 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176054246 | GCTCACTGCAACCTC[C/T]GCCTCCCAGGTTCAA | 64326 |
rs554898426 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176150121 | GATGATAAGAATAAG[C/T]CAATTAAAATCTGAA | 64326 |
rs554911365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175959459 | TGGCCATCAAAATAC[A/G]GCAAATGAATAAAGA | 64326 |
rs554914720 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175994462 | GGCAAACTGGATAAA[C/G]AGTCAAGACCCATCA | 64326 |
rs554933875 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176187941 | AGATTTTTAGGTCAT[A/G]AGGGCAGAACTCTCA | 64326 |
rs554940621 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176053320 | TAGCTTCTTCGTCAT[G/T]TTTCTCTCTTCTCCC | 64326 |
rs554957330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176100731 | TATGCACCCAAATCT[C/T]AGCAGGCATAACTAT | 64326 |
rs554969752 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176138254 | TGCTTAACATCAATA[A/C]GTATAGTCAGAAGAG | 64326 |
rs554977936 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175999625 | CTGTTGGGTATATAC[C/T]CAGCAGTGGGACTGC | 64326 |
rs554991010 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176093824 | GCCTAGGTGACAGAG[C/T]GAGAGACTCTGTCTC | 64326 |
rs554992712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176179022 | AAGGCCGGGTGCAGC[A/G]GCTCACGCCGTAATC | 64326 |
rs554994744 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176054673 | CATCCTTGCTTACCT[A/T]CTCAAGGATTGTTTC | 64326 |
rs555003953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175999165 | AATTATTATTGACTA[C/T]AGTCACCTCGTTATG | 64326 |
rs555009741 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176103739 | AAATTAAAAGTTTAA[C/T]TTCAAATTTTTAAAA | 64326 |
rs555023371 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176111047 | GCCCCAGCTACTTGG[A/G]AGGCTGAGGCAGGAG | 64326 |
rs555024085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176133202 | CGTACGTATATGTAC[A/G]TATGTACACACATAC | 64326 |
rs555032638 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176126056 | CTACTGATTTTTTGT[A/G]TGTTGACTTTGTATC | 64326 |
rs555037233 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175976104 | TACAAAACAAAAAAC[A/T]TTGAGAAAATAAGAA | 64326 |
rs555037999 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176152537 | ACTGCAGCCTCCGCT[A/C]CCCAAGGTGAAGCAA | 64326 |
rs555055254 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176047799 | AATATTTCAGGCTGG[G/T]TTCGGTGGCTCATGC | 64326 |
rs555059713 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175952092 | TCCCATCAGCAAGAA[C/T]GCAAGCCAGAAGACA | 64326 |
rs555068418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176195078 | GGTGACAGAGTGAGA[C/T]CCTGTCTCAAAGAAG | 64326 |
rs555070794 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176008250 | CCACTGTCTGGCACT[C/T]CCTAGTGAGATGAAC | 64326 |
rs555071848 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175977934 | CCAATATTCACTTTC[C/T]TTCTTTCTACTATTA | 64326 |
rs555073647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176145694 | TCATATACAACCATG[C/T]GGATGAATCTTAACA | 64326 |
rs555081558 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176080106 | AAATGGAAATTAAAA[G/T]GTATTTTGATATATA | 64326 |
rs555084590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176138239 | GGCAATAAATAAAAC[C/T]GCTTAACATCAATAA | 64326 |
rs555099375 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175948132 | GAGAATATATGTGGT[G/T]AAGTATTTTTCTATT | 64326 |
rs555108816 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176089785 | CCCTATATAATCTCT[C/G]TTAGTTTTCAACCTG | 64326 |
rs555130148 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175994134 | CCAGAATTTCATATC[A/C]AGCCAAACTAAGCTT | 64326 |
rs555147538 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176069735 | ATCCACTCTCTTCTT[A/G]TTTCCTTATATTACC | 64326 |
rs555149943 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176097789 | CGGGACAATCGCTTG[A/C]ACATGGGAAGCGGAG | 64326 |
rs555199140 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176006715 | GTTTCTGCCGAGAGA[G/T]CCGCTGTTAGTCTGA | 64326 |
rs555201584 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176160569 | GAACTTTGAACAAAT[A/T]TACAGGAAAAAAAAT | 64326 |
rs555205060 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176135392 | TAAATATTTTAAATG[A/C]CATGTACATTATACT | 64326 |
rs555224999 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175960244 | TAAATGTCTTTGGAG[A/T]CTGAAAGATTTCAAT | 64326 |
rs555229004 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176041142 | TTAAATACAATGCAG[C/T]ACATAGAGATTTCTA | 64326 |
rs555231174 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176155824 | TGACTACTGATTTCA[C/T]CAGAAACAAAAGAAT | 64326 |
rs555239873 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175944887 | TTCAAAAGAATTTGT[C/T]TCCCTATCACAAAAA | 64326 |
rs555240474 | in-del | -/AA | 0.0197687 | 0.0974348 | intron-variant | RFWD2 | GRCh38.p7 | 1:176097227 | GACCTTGTTTTGTTG[-/AA]AAAAAAAAACGACTG | 64326 |
rs555246404 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176037526 | AAAACAGAAAAAAAA[A/C]AACAAAAAAATTCAC | 64326 |
rs555254337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992610 | TCCCGCACCTGGCTC[A/G]GAGGGTCCTACGCCC | 64326 |
rs555257187 | snp | C/T | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176186088 | CTACAAAGGGACCCA[C/T]AGTAAAGAAAACTGA | 64326 |
rs555286359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175952642 | AGGTGGGCATGGTAG[C/T]TCACACCTGCAATGC | 64326 |
rs555295647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176089129 | AAGATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 64326 |
rs555317959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176040612 | ACCATGCCTGGCTGA[C/T]GAGTTCTTAAATCAA | 64326 |
rs555318857 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175987584 | TTCCATTTCTCAGTA[G/T]AGGAATTATTCTATT | 64326 |
rs555327444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176122847 | TATAAAAAGCAAGCA[C/T]GAGGGAAAATTTCTA | 64326 |
rs555334290 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176007064 | TTTTTATTCTTTTTT[C/T]TCTAAACTTCCCATC | 64326 |
rs555336061 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176189548 | CAAACACAAATTTAA[C/G]AGAATTTGCTGCCCA | 64326 |
rs555337512 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176139070 | CTACAAGGAACGTAA[A/G]TAAATGAAAAACAAA | 64326 |
rs555345245 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176134457 | AAACCAGGCTTTATT[C/T]TAAAATCTTGGGAAA | 64326 |
rs555397609 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176191345 | TATCAGCACATAGAA[C/G]ACCTTGGAAAAATTA | 64326 |
rs555401380 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176128404 | TTTGTTTTTGTTTTA[C/G]TTCACAATCAAGATT | 64326 |
rs555406281 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176002394 | AGTTTTAGGGTACAT[C/G]TGCACATAGTGCAGG | 64326 |
rs555410449 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | RFWD2 | GRCh38.p7 | 1:175995801 | AGATGGATTCACAGC[C/T]GAATTCTACCAGAGG | 64326 |
rs555412136 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176138055 | GGGTAAGAAGAGGAC[C/T]AGATAACTAAAATTT | 64326 |
rs555441550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176032757 | TTTAGAAGAGACATC[C/T]ACTGGTCACATAAAT | 64326 |
rs555466800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176137245 | GCAAACATTGTAACT[A/G]TTGAATAACACTTAA | 64326 |
rs555476874 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176055100 | TGACAACTCCATCAC[A/T]GTCTACTTTGGTCAT | 64326 |
rs555495720 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176019423 | AGCTGAGACCATGCC[A/C]CTGCACTCCAGCCTG | 64326 |
rs555501592 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176035436 | ATACACTAACATAAT[A/T]AAAATCCCAGAGGAG | 64326 |
rs555505639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176083663 | ACTCCAAAGTAATAG[C/T]TCTTTAATATTCATC | 64326 |
rs555515633 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176153490 | AAGAAGCTTGTCGGC[C/T]GAGACTATGGGATTT | 64326 |
rs555516562 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176096996 | TGTGCAACCTTTGCT[A/T]TTTGTTGATTCTCTT | 64326 |
rs555535212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176171089 | GAGATCACACCACTG[C/T]ACTCCAGCCTGGGCA | 64326 |
rs555537745 | in-del | -/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176096669 | TTTTACGTGAGAGGA[-/T]TTTTTTTTTTCCTTT | 64326 |
rs555544415 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176111572 | TGCTGGGATTACAGG[C/T]GTGAGCCACCACACC | 64326 |
rs555545568 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176151846 | TATTTCACTATAAAT[A/G]AGTAATTTGGTCCTT | 64326 |
rs555560133 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176088159 | ACCTAATGTAAATGA[C/T]GAGTTAACGGGTCCA | 64326 |
rs555576643 | in-del | -/G | 0.0244538 | 0.107838 | intron-variant | RFWD2 | GRCh38.p7 | 1:176113950 | CAGGGTAGGGTTTTT[-/G]TTTTTTTTTTATAGT | 64326 |
rs555585076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992920 | GCAGCTGGAGATCTG[A/G]GAACGGGCAGACTGC | 64326 |
rs555597478 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175960273 | ATTCAAAGCTCTAAC[A/G]CTTCTAGACTTTTCA | 64326 |
rs555614766 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176123304 | GTAGGAGAGATGTCA[C/T]GAACAGCAGAAATGG | 64326 |
rs555618689 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176025603 | CTCATTGAAAGACAG[A/T]AAACAACCCAAACAA | 64326 |
rs555622511 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176020323 | CTCGGAAAAAAAAAA[A/C]AAAAAAAACCTTCAT | 64326 |
rs555650569 | in-del | -/AA | 0.309648 | 0.24278 | intron-variant | RFWD2 | GRCh38.p7 | 1:176181427 | TTTAAACAAAACTGC[-/AA]AAAAAAAAAAAAAAT | 64326 |
rs555678956 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176110016 | CTAGCGGTATTTTTT[G/T]AGTGCACTGATTTTT | 64326 |
rs555679469 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176131504 | CTGACATATAATAAA[G/T]ATATTCATTATAGAA | 64326 |
rs555682737 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176018917 | ACGCCTGTAATCCCA[C/G]CACTTTGGGAGGCCG | 64326 |
rs555694241 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176035188 | TGTAATTATACTCCA[C/T]GGGGTAAAAATAAAC | 64326 |
rs555694795 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176061416 | CAGATCACCTGAGGT[C/G]AGGAGTTCGAGATCA | 64326 |
rs555717658 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176119774 | TAGATGGCAGTAACA[A/G]TATCAATAGTACCAT | 64326 |
rs555723566 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175993649 | AAGGGTATCAGTGAT[A/G]GAAGATGAAATGAAT | 64326 |
rs555738645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176124447 | TTTCCCAGCTTCTGG[C/T]AACCATCTTTCTATT | 64326 |
rs555756554 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176044636 | AATTAAGAGACACAT[A/T]TTGAATTTAGGTAGA | 64326 |
rs555766907 | snp | C/T | 0.00036245 | 0.0134571 | synonymous-codon | RFWD2 | GRCh38.p7 | 1:176081199 | ACTAGCATATGACAA[C/T]GTGGCTAAAGGTCGT | 64326 |
rs555767261 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176171453 | GCTGGTATATATCCA[A/G]ACTACTAAACTTTCT | 64326 |
rs555791190 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176125354 | CCCCAATGTTTTCTT[C/G]TAGTAGTTTCACAGT | 64326 |
rs555807388 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175999012 | TATGACTCTCTATTT[C/T]GTTTTATGTCTTTCC | 64326 |
rs555818960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176039068 | GAGGACACACCACAT[C/T]CTGGGGCCATAAAAC | 64326 |
rs555828839 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176005731 | ATAGTTTGTTATAAT[C/T]TCTGTTCTTTTACAT | 64326 |
rs555832426 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:176171901 | TCTGGTATTGAATAA[A/G]AAGCTTACTTATATA | 64326 |
rs555877591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175958398 | TATCAAAGCCATTTC[A/G]GCTATGAAGCTAAAT | 64326 |
rs555882301 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175975500 | CTGCAATCTCTGCCT[C/T]CTGGGTTCAAGCGAT | 64326 |
rs555882700 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176010718 | TATTTCAGTTGTTAA[C/G]CCAAATGATGCTATC | 64326 |
rs555885796 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176046602 | ATTCAGTTCTAATAA[A/C]CATATTACAGCTTAC | 64326 |
rs555886087 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176184151 | ATTTTAAAATTAAAA[A/G]ATTTTTTTGATGTAT | 64326 |
rs555940879 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175958963 | CTTAATTTGCTTTAT[G/T]AAGTTAATATACCCA | 64326 |
rs555947587 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176200617 | TTCTATGTTTCACTT[G/T]ATATAGAAACAGAGG | 64326 |
rs555950738 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176134926 | GGGGTTTCATACACT[C/G]CATGGAAAAGGCTCC | 64326 |
rs555962021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176077825 | AATACAAAATCGATG[C/T]ACAAAACTTGGTAGC | 64326 |
rs555987933 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175961520 | ACCATAGGCCAACAG[A/G]GGAAATGGACTTTTA | 64326 |
rs555993788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176197896 | TCGAAATTAAAAGAA[C/T]AACATTTAGAACACC | 64326 |
rs556001378 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176087179 | AACCTAGGCAGTACC[A/T]TTCAGGACATAGGCA | 64326 |
rs556003964 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176120330 | GAGGCTGAGGCAGGA[C/G]AATCTCTTGAACCCA | 64326 |
rs556021173 | in-del | -/TG | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176160124 | ATCTAATAAGACAAC[-/TG]TGTTTCTTCAATTCG | 64326 |
rs556031020 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176103619 | CATATCACAGCTCAA[A/G]AAGTTTCAAATCTTG | 64326 |
rs556031176 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175970061 | TCCTAGAAAACTAAG[C/T]AGCTCTTACTCTGGT | 64326 |
rs556032670 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175980568 | TCAGAGAGGGGAAAT[C/T]TGGAAATCTGTTATC | 64326 |
rs556053012 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176060742 | CTAACGTGGAGCAAA[A/C]ATTTACAGTTTAGAA | 64326 |
rs556058736 | snp | C/T | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176144677 | TACAAGGTGGTATTG[C/T]GAAAAAGACCAGTGA | 64326 |
rs556065657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176204273 | AACATCACAGAATTG[C/T]TCTAAGGATAAAATA | 64326 |
rs556072839 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176023446 | TAAACAGGCCAGGCG[G/T]GGTGGCTCACGCCTG | 64326 |
rs556080490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176008303 | AGAAATCACCCATCT[C/T]CTGCGTTGCTCATGC | 64326 |
rs556083688 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176029868 | CATTATCAAAAAATA[A/T]TGCTAATTTACAATC | 64326 |
rs556087637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176078220 | GAACATACCTGGAGG[C/T]ATCACACTACCCAAC | 64326 |
rs556118448 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175986515 | CTTAATTAGAGGACC[A/C]TATAGGCCACTATCC | 64326 |
rs556122924 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176068522 | ATTTACGTAGTATTT[A/C]CAACATGCCATATAA | 64326 |
rs556128872 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176204942 | CAAATACAAATTTTT[A/C]CTCTTTTAAAAAAAG | 64326 |
rs556152980 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175994787 | TTAGACTCCCACACA[A/G]TAATAATGGGAGACT | 64326 |
rs556161997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176154603 | ACACATGGACACATA[A/G]AGGGGAACAATACAC | 64326 |
rs556162274 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176082582 | GAGGCCGAGGCAGGC[A/C/G]GATCACCTGAGGTCG | 64326 |
rs556164543 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176098390 | GGTGTGGAAATGTAA[A/T]TTTTTGCCTAGGGTC | 64326 |
rs556166064 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176073633 | TTGCTAACCTAGGAC[A/C]ATCTTCTACTTATGA | 64326 |
rs556170793 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175974612 | AAAACGTTTAAGATC[A/G]AATAGGTAATTTCAG | 64326 |
rs556179316 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176133179 | GTATGTACACACATA[C/T]GTATATACGTACGTA | 64326 |
rs556186451 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176106821 | TCTGTCTTGATAAAT[G/T]GACTCTGTCTAGGCA | 64326 |
rs556195445 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175981231 | TTACCACTGTCTAGA[G/T]ATTTTCACTGGATGT | 64326 |
rs556200362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176072238 | TATTTTTCAACAAGC[A/G]AATATGTGGACATAT | 64326 |
rs556204832 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175983733 | CCAAAATGCTGATAA[C/T]GATGGACATGAAATC | 64326 |
rs556213434 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176057450 | CCTGATTCTCCTGCC[C/T]CAGCCTGCCGAGTGC | 64326 |
rs556227849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176070617 | CAGTGAGCCAAGACC[A/G]CACCACTGCACTCCA | 64326 |
rs556263000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175982029 | ATGAAAGATAACAAG[C/T]GTTGGCAAGAATGTG | 64326 |
rs556271154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176199547 | TTTAACTAGCAAATA[C/T]ATAAGCAGTTCATGT | 64326 |
rs556277575 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175954449 | AAAACCAGAAAAAGG[G/T]AAAAAAGTATTGAAA | 64326 |
rs556282813 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176105446 | CAAACGGAATTTCAA[A/G]GAAATATCTCTAGTT | 64326 |
rs556288531 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176155609 | TAAATCCTAGGCATT[G/T]AATTTGTTCGCTGCC | 64326 |
rs556299183 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176056953 | TATTTTTGCCCTTAC[A/T]CTTCCAATCCTACTC | 64326 |
rs556311090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176107603 | CTAATAAATGTGGAA[A/G]ATATAAAAACTCAGA | 64326 |
rs556328140 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176192433 | CATTAATGTGACTAA[C/T]ACTTTTCTGCTTCTC | 64326 |
rs556338953 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175955163 | GAGGTGGGAGAATCA[C/G]CTGAGCCTGGGAAGG | 64326 |
rs556339675 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176057907 | GCGTCTCTGCCCGGC[C/T]GCCCATCCTCTGAGA | 64326 |
rs556343704 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:176026574 | TAAATTCTATATGCT[-/A]AAAAAAAAGAGAATT | 64326 |
rs556344324 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175998253 | ACTCATAGGTGGGAA[C/T]TGAACAATGAGAACA | 64326 |
rs556382515 | in-del | -/CAGA | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:175977685 | AAAGTTTCTTTTCCC[-/CAGA]CAATCTGTATATTCT | 64326 |
rs556407671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176063208 | GGGACTACAGGCGCC[C/T]GCCACCGCGCCTGGC | 64326 |
rs556424406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175977143 | TACACAATCTATTCC[C/T]TAAAGCTTTCTACTT | 64326 |
rs556425098 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176113247 | ATACCATTCTAACTA[C/T]GGTGAGATGATATCT | 64326 |
rs556434025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175975168 | TGTATCTAAAATACA[C/T]AGGATATATAAAAGC | 64326 |
rs556465780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176180454 | AGTGCTCAACAACAG[A/G]TGGGCATAACAAAGA | 64326 |
rs556470722 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176003005 | CTATTTCTCCACATC[C/G]TCTCCAGCACCTGTT | 64326 |
rs556474035 | in-del | -/C | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:175955137 | CTGTAGTCCCAGCTA[-/C]CCAGAAGGTTGAGGT | 64326 |
rs556491492 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176064962 | TAGCTACCACTTCTT[G/T]CTGTTGCCGTTTAAC | 64326 |
rs556500107 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176158591 | AAAATACTACAATGG[A/C]CAGGAGAGAGAAAAT | 64326 |
rs556514438 | snp | C/T | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176202111 | GTACCCAGTGAGAAA[C/T]ACATTCCACATACAT | 64326 |
rs556520641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176085218 | TGAAATCCCTACACT[A/G]ATCATTCCCTTACAC | 64326 |
rs556521314 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176112041 | TCAGCTCTTCTTCCA[C/T]AAGTATTTTCTCTTT | 64326 |
rs556533714 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176063783 | AATACACAAATAGGA[A/C]ACTTTCTGCTATACA | 64326 |
rs556535828 | in-del | -/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176085259 | TCAATTCGGCCTGGA[-/T]TTTTTTTTTTACTAT | 64326 |
rs556556328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176106005 | ACTTTGGGAGGAACT[C/T]AGTTTACAGGTTTGT | 64326 |
rs556563222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176153304 | GGAATAACAAAATAA[A/G]GCAATAAAAAATACT | 64326 |
rs556574844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175972275 | AACAGACCATACTTT[A/G]AAAAATACTAATACA | 64326 |
rs556579227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176190643 | GTCATATTGCAATCC[A/G]GCCCAAGTAACATCG | 64326 |
rs556581690 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:176141511 | ATCTCAAAAAATACA[C/T]ACATACATACATACA | 64326 |
rs556582621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175988116 | AGGGAAGGACTAATG[C/T]TCTTCTAGTACAACA | 64326 |
rs556588159 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175961281 | TTTGGAGAACCCTGA[C/G]TAAGACATAAAGAAA | 64326 |
rs556597159 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176028201 | GACACAGCCAAACCA[C/T]ATCACTGAATGACTG | 64326 |
rs556608023 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176099239 | AAATACAGGTTTCTA[A/G]TAACTTTGGAGATTG | 64326 |
rs556610820 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175981068 | TACCTAACTCCAGTC[A/T]CTAGATAAATCAATG | 64326 |
rs556613019 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176139523 | GTATTTGTATGTTCA[G/T]CATAGCTCTATTCAT | 64326 |
rs556630942 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175998544 | AAAATGTTAAAAAAT[A/T]ATTATCTTCTGTGAA | 64326 |
rs556643258 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176079787 | TTAACCACTGCTGAA[C/T]GTGGGTGATGGTTAT | 64326 |
rs556650187 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207227 | GCCGCCGCCGCCACC[A/G]CGGTCCCTGTAGCAG | 64326 |
rs556667167 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176117692 | CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGACC | 64326 |
rs556670510 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176069424 | TAGTCTACTCCCACA[C/G]TATTTTATTGACTTG | 64326 |
rs556683611 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176167357 | AATGATCAGTGTCTG[C/T]CTTGTCCACCATCGT | 64326 |
rs556684072 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176150898 | TAAAGGAAGAATTTC[A/T]AGAAAAGAGATGAAT | 64326 |
rs556689087 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175962280 | AGAGAGGAATTCCCT[A/G]TACCCCAGTTACTTC | 64326 |
rs556698338 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176060388 | ACAACATCTAGTAGA[A/G]AAAATAACAAGAGCT | 64326 |
rs556700997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176187196 | CTGGCATGATCATGA[C/T]TCACTGCAACTTCGA | 64326 |
rs556711256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176003659 | AGAGATCAGATAGTT[A/G]TAGATACGTGGCGTT | 64326 |
rs556736380 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176021257 | CTTCCAAATTTTATT[C/G]GTTTTTAGAAATATA | 64326 |
rs556740908 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RFWD2 | GRCh38.p7 | 1:175985168 | CAGTTAAAATTTTCA[A/G]TCTTGTCTTTCATCT | 64326 |
rs556748714 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176034234 | TAAAGTCAGCACCTC[A/C]AGCAACAAACACTAA | 64326 |
rs556763045 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176005608 | CTTCATTTCGTTATG[C/T]ACCCAGTAGTCATTC | 64326 |
rs556766425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176180987 | TAAATCAGGGCTTGG[C/T]AGACATACGGTACAG | 64326 |
rs556767340 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176042482 | GCAGGAGAATCGCTT[C/G]AACCTGGGAGGCGGA | 64326 |
rs556780550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175995158 | CTACCGGGTACATAA[C/T]GAAATGAAGGCAGAA | 64326 |
rs556826295 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176002536 | AACAGTCCCCAGAGC[A/G]TGATATTCCCCTTCC | 64326 |
rs556831750 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176008118 | TTTTCCAGGTGCGTC[C/T]GTCACCCCTTTCTTT | 64326 |
rs556842897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176174083 | TCCTTCCATACTCAT[A/G]TATAACTCTCTCTCA | 64326 |
rs556848737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176049363 | GTTTTGATTTCATTG[C/T]TATTATTTTCTTACA | 64326 |
rs556859877 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176001517 | ATGTAAAAATAATAA[A/T]AAAAGCGAGATATTT | 64326 |
rs556862198 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176096425 | GGTGCATGGCCATGT[A/C]TGCCACATGAGTGCA | 64326 |
rs556901387 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175950176 | AGGGTTAACTCTTAA[C/T]ACTATTTCCTGCAGA | 64326 |
rs556909376 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176037705 | AACTACATGATGATA[C/T]GTGCATAAAAAGTAT | 64326 |
rs556922230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176005945 | TCTAATGTTGACAGT[A/G]GGGTGTTAAATCTCC | 64326 |
rs556932460 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176053411 | TCCTCTACCAACCCA[C/T]GAGTTCTTGGAAATT | 64326 |
rs556936591 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176050054 | AGATTTATAAAAATT[G/T]ACTGCATGACAAATT | 64326 |
rs556945467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176006304 | TGACTCTTTATCCAA[C/T]TTGCCAGTCTGTGTC | 64326 |
rs556961377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176150301 | AGAAAATATGAACTG[A/G]TAATCACAACAGGAT | 64326 |
rs556968354 | snp | A/G | 9.91064e-05 | 0.00703871 | synonymous-codon | RFWD2 | GRCh38.p7 | 1:175987015 | TTTTCGGTCTTTGTC[A/G]AGAACACTTTTGACT | 64326 |
rs556979175 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175983433 | ATGCCTTTCACCTTC[A/C]GCCATGATTGTGAAG | 64326 |
rs556986586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175965876 | CGTGAGCCACCGCAC[C/T]CAGCCACTTATCTGG | 64326 |
rs556989673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176009684 | TATACCAGTTAATCC[A/G]ATTATTGTTATTATT | 64326 |
rs557009438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176121110 | TAATAAATAAACCAA[A/G]TGGGGCTACAAATAA | 64326 |
rs557025331 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176086678 | TTGTGAAAATGGCCA[C/T]ACTGCCCAAAGTAAT | 64326 |
rs557043470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175964682 | AGTCCTTTAACAAGC[A/G]TTTGATTAAATGGAA | 64326 |
rs557048267 | in-del | -/TCTT | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176168962 | TATTTGGTTTCCAAC[-/TCTT]TCTTTTCATCAAAAT | 64326 |
rs557069883 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | RFWD2 | GRCh38.p7 | 1:176005197 | TGGGATCGGTGGTGA[C/T]ATCCCGTTTATCATT | 64326 |
rs557077464 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176091443 | AAAATAAAAAAAGAG[A/T]GCAAGGAAACGAGCA | 64326 |
rs557078132 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176037481 | TATGAGGCCAGCATT[A/G]CCCTGATATCAAAGT | 64326 |
rs557084450 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176177494 | AAACCACAAAAGACA[A/T]TCCCCACAATGTTAA | 64326 |
rs557126217 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176017855 | ATAGCAATACTTAAA[C/T]CATTTTTTACTTCCT | 64326 |
rs557133391 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176129289 | GAAATACAAATAAAA[C/G]GTATGTCTCAAAAAT | 64326 |
rs557137893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176074037 | GTTCAAGCTATTCTC[C/T]TGTCTCAGCATCCCA | 64326 |
rs557140622 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176115777 | AAATATAAAAATAAA[A/C]AGTCGAAAAAAGCCT | 64326 |
rs557140850 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176088920 | GAATCACTTGAACCC[A/G]GGAGGCAGAGGCTGA | 64326 |
rs557141656 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176066032 | CACCTGGCCGGGGGA[C/T]AATGATTTTATCACA | 64326 |
rs557147442 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176150585 | TATCTACGATTATTT[A/G]TCTAGAGGACAAAGA | 64326 |
rs557168088 | snp | A/G | 0.000943396 | 0.0216981 | intron-variant | RFWD2 | GRCh38.p7 | 1:176081295 | ACTGTCATCTATATG[A/G]AAAAAAAAAAAAAAA | 64326 |
rs557196452 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176181733 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 64326 |
rs557204686 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, synonymous-codon | RFWD2 | GRCh38.p7 | 1:176133870 | TATTCCATTGACAAA[G/T]ATCCTGTGCATATCA | 64326 |
rs557214831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176086079 | GAAACCAAATTCATT[C/T]GCAGAATGATTAAAA | 64326 |
rs557225605 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176183558 | GCAGTTTCTCAAAAA[A/T]TTACAAACAAAATTA | 64326 |
rs557237498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176080646 | AATAATTGTACGCCA[A/G]TAAGTTCAACAGCCC | 64326 |
rs557244224 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176170295 | GGTGAATCCTTTCCA[A/C]AAGGTTTTCCATTTA | 64326 |
rs557247303 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176164143 | CCTTACATGTTTCTC[A/C]ATGATGACGCTATTG | 64326 |
rs557249362 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176034585 | CCTTCTTGACAAAGT[A/G]TCAGTAAAAGGGGGC | 64326 |
rs557277250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175948991 | AATATGGTGTAATCC[C/T]GTCTCTACTAAAATA | 64326 |
rs557288118 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176045948 | GATTAAGTGAAAGAA[G/T]AACTTTAATTTGGCA | 64326 |
rs557296407 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176024905 | CTACACTGAAAATTA[C/T]AAAACTATTGATGAT | 64326 |
rs557296924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175956714 | CATATATGATGGTGG[C/T]CCAATAAGATTATTG | 64326 |
rs557299865 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176041750 | GTGGGTAGATCACTG[C/G]AGGTCAGGAGTTCGA | 64326 |
rs557301944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176046780 | AAATAAATTAGTATA[C/T]AATTTGAATTACTGA | 64326 |
rs557308827 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176182182 | CAAGAAAATTAAAAA[A/C]CTCACTTCACAATCT | 64326 |
rs557318921 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175965032 | AAATAAAAGACCATA[C/T]CTGCCTTAAGCTCTT | 64326 |
rs557329551 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175966759 | GCTCCTAAAAGCCTT[A/G]TTACATGGAAAATTT | 64326 |
rs557354196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175957543 | GATGAAATCAAATCA[C/T]CTAATGGCATTTCTC | 64326 |
rs557360293 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176175473 | GGCATCAGATTCTCA[C/T]AAGGAGCGTGCAACT | 64326 |
rs557372511 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176016733 | TTTTATGAATGACTC[-/T]TTTTTTAAAAAAAAA | 64326 |
rs557380111 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176051622 | CAGCCGCAGGCAGGT[A/C]CTTCAGGAGGTATTC | 64326 |
rs557397130 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | RFWD2 | GRCh38.p7 | 1:176004927 | GTTTCAGAAGGAATG[A/G]TACCAGTTCCTCCTT | 64326 |
rs557402818 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176209002 | GAGAATCGCTTGAAC[A/C]CAGAAAGCGGAGGTT | 64326 |
rs557418868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176146116 | ATATTACAGTAAATT[C/T]AATAGGTATCAAAAA | 64326 |
rs557422528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176138303 | TGGTAGAAAACACCA[A/G]TGTTAAAGAGATGGG | 64326 |
rs557433274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176179565 | GTGGTGAAACCCCAA[C/T]TCTAAAAAAATTTTA | 64326 |
rs557438358 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175963666 | CTTTTGTCCAGGTAC[A/C]TTCCTTTCCCTTTGT | 64326 |
rs557455312 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175954575 | TCACTAGATATTCTA[C/T]AGATATTAAAAGAAT | 64326 |
rs557457684 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176139295 | AAAAAAAACAAAAAA[A/C]AAAAACAAAAAAAGA | 64326 |
rs557464657 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176148469 | ACTATTTAATTTTCC[C/T]ATATTTTGTATAGTG | 64326 |
rs557480123 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176063145 | GCTCACTGCAAGCTC[C/T]GCTTCCTGGGTTCAC | 64326 |
rs557480207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176168143 | GCTCACCGCAACCTC[C/T]GCCTCCTGGGTTCAA | 64326 |
rs557482697 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176131592 | AAACTTTTTAGTGAG[A/G]AATAAGAACAAAAAC | 64326 |
rs557489842 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175970364 | TACGAGTTTAGAAGC[C/T]GGAATGGGAATAGTA | 64326 |
rs557496744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176173373 | AGGCACAATGGCTCA[C/T]ATCTGTAATCCCGAC | 64326 |
rs557516778 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176103192 | TCCTGAGTGATATCA[C/G]CATCTTTTGTTATTC | 64326 |
rs557539278 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176063312 | TGATCCACCCGCCTC[A/G]GCCTCCCAAAGTGCT | 64326 |
rs557543833 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176086164 | AAACATCTTCACTTC[C/T]ACAAATAAAATGAAG | 64326 |
rs557550904 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175963205 | GATTATCTTCACAGT[A/G]GGCTTTAGGCATTTA | 64326 |
rs557554457 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175954942 | AAATATATATATATA[-/T]ATTCACTATGTAAAG | 64326 |
rs557561964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176048654 | TTAATTTAGGAGGTT[C/T]TGGTATAGCTGAGAC | 64326 |
rs557578738 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175984599 | AGAGGGCCACCATCC[A/G]CCAGACCCCAAAATG | 64326 |
rs557580108 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175960265 | AGATTTCAATTCAAA[C/G]CTCTAACGCTTCTAG | 64326 |
rs557582849 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176127430 | TTTAGATTCCGCATG[C/T]AAGCAAGATCATACA | 64326 |
rs557601124 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176001917 | TAAACATATCCTACT[A/G]CCTGCTGGCAGTAAT | 64326 |
rs557618636 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175944931 | CCAAGAGCAGCAATG[C/T]CCATGGAGTTACATT | 64326 |
rs557618689 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176065731 | TTTTTTTTTTCAGAC[A/G]GAGTCTTGCTCCGTT | 64326 |
rs557624823 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176126511 | CACCAGGCTGGAGTG[C/T]GGTGGCGCAATCTCA | 64326 |
rs557625233 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176021306 | CCAGAAGTAAAAGCA[C/T]TAAAAAACACACTCA | 64326 |
rs557639375 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176070772 | TCCTTCCACCTCACC[C/G]TCCTCATTAGGACTA | 64326 |
rs557651446 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175960309 | GGCAAGTTACTTGAC[A/C]TCTCTGAATCTCAGT | 64326 |
rs557657287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175945652 | TAGCGTCCAGATACT[C/T]TGTATTTTTAGAATT | 64326 |
rs557657914 | snp | G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207283 | CGTGCGCGCGCGCGC[G/T]AGCGGCGGAAGAGGC | 64326 |
rs557711294 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175961105 | TGGGACTTGCATCAA[C/T]GGGCCCTCAAATTCT | 64326 |
rs557719499 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176002836 | GTGCATGTGTCTTTA[C/T]AGCAGCATGATTTAT | 64326 |
rs557726096 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176121301 | CAAAATTGTTGTGGC[C/T]CCAATTTTGCAGAGA | 64326 |
rs557729947 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176193302 | GTGGAGAAATTAGAA[C/T]CCTTATACATTGCTA | 64326 |
rs557765288 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175996216 | TTTGTGCTAAAAACT[C/G]TCAATAAATTAGGTT | 64326 |
rs557776399 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175997529 | ATATCCAGAATCTAC[A/T]ATGAACTCAAACAAA | 64326 |
rs557783032 | snp | C/T | 1.65507e-05 | 0.00287664 | missense | RFWD2 | GRCh38.p7 | 1:175988297 | ACTTACCACAAGCTA[C/T]ATAATCTCCATTGGA | 64326 |
rs557786133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175995608 | CTACCATCAGAGAAT[A/G]CTACAAACACCTCTA | 64326 |
rs557786183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176122898 | TCTATTGCTTTATCA[C/T]TTTTGGAAGTAAACT | 64326 |
rs557796726 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175980930 | TGTCCCTTTACACAG[A/G]CATCATCACATAGGA | 64326 |
rs557811709 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176028309 | GTGGCTCATGACTGT[A/T]ATCACAGCACTTTGG | 64326 |
rs557823944 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176026296 | ACAGAACATACACTC[A/C]AACTCAATAAACTAA | 64326 |
rs557826599 | in-del | -/T | 0.00279329 | 0.0372672 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176184718 | AGAAAAATAATTGAT[-/T]TTTTTTTTAAAAGTA | 64326 |
rs557828342 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992689 | GGCGGCAGCGAGGCT[G/T]GGGGAGGGGCACCTG | 64326 |
rs557838380 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176075690 | CTCGGCTTACAAGAA[C/G]ACTTAGCCACACAAT | 64326 |
rs557847484 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992395 | GCCAGACAGTGGGTG[A/C]AGGAGAGTGGGTGCA | 64326 |
rs557856350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176098272 | CCAGGTTTTAAAGGT[A/G]AAATTGCTAAGAGTT | 64326 |
rs557862011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176131067 | AGGCAAAAGGAACAG[C/T]GTAAGCAAAGATACC | 64326 |
rs557874167 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175990599 | TTCAACAACTTCAGT[A/C]AAAATATCTGTTTTT | 64326 |
rs557878670 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176129290 | AAATACAAATAAAAG[C/G]TATGTCTCAAAAATG | 64326 |
rs557893450 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176006021 | GACTTGCTTTATGAG[C/T]CTGGGTGCCCTTGTA | 64326 |
rs557907663 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176077635 | CTATTCAACATTATA[A/C]TGAAGGTCCTAACCA | 64326 |
rs557925922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176012636 | TCCAATTCTGCAAGC[A/G]CCATTCATGGTAAGT | 64326 |
rs557927151 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176141229 | GAGCAAGGCTAGGTG[C/T]GGTGGCTCACGCCTG | 64326 |
rs557931839 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176148077 | TTCTTCTTTCCTACC[A/G]CAAAAAAAAAACCTG | 64326 |
rs557935334 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176173759 | TTGGGAGGCTGAGGC[A/G]GGAGGATCGCTTGAG | 64326 |
rs557940406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176071284 | GCTCCCACTTCACCT[C/T]CCACCATGATGATGA | 64326 |
rs557952521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176021943 | TACTTGTTAACTTTC[A/G]TGTTCACATCTTTAT | 64326 |
rs557963871 | in-del | -/A | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176042111 | GCGAGATTACGTCTC[-/A]AAAAAAAAAATTAGC | 64326 |
rs557974090 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175977712 | TATTCTTAAATTAGT[-/A]AAAAAAACCTTTTTT | 64326 |
rs557993097 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176116878 | CAATTTACCACTTCA[A/C]CCCACCACCTCAAAC | 64326 |
rs558012978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175988717 | ACGTGCCTGTAGTCC[C/T]AGCTACTTGGGAGGC | 64326 |
rs558018774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175953568 | TTTGAGATCAGCTTG[A/G]GCAACAAAGTGAGAC | 64326 |
rs558022842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176173816 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAC | 64326 |
rs558031775 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176110856 | TTCTCAATAAAAAAT[A/T]GTAATAGAATTTATC | 64326 |
rs558032234 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176152583 | CTCCCAAGTAGCTGG[G/T]ATTACACATTCGCAC | 64326 |
rs558068508 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176120586 | GTGAGAAGCTTTGCT[-/A]AAAAAAAGTAACAAC | 64326 |
rs558098183 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176008065 | GCCGTTTTTTAAGCC[A/G]GTCGGAAAAGCGCAG | 64326 |
rs558104006 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176097697 | AGCATGGTGAAACCC[A/C]ATCTCTACTAAAAAT | 64326 |
rs558106185 | in-del | -/AT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175988983 | AATACACAGTAACAC[-/AT]GAGTTGACTTTAATA | 64326 |
rs558126538 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:175980599 | CTGATCCCTGCCTCC[C/T]CTAACCCTAAAGCTA | 64326 |
rs558127421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176117878 | CCAGCCTGGGCAACA[A/G]AGCAAGACTCTGTCT | 64326 |
rs558169813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176159120 | GTTCTCCAACTATAA[C/T]GGAATTCAACTAGAA | 64326 |
rs558180556 | in-del | -/ACC | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176010079 | ACAGCACAATGAATA[-/ACC]ACCTTGTACCACTTG | 64326 |
rs558183726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176198766 | ACTTACAACGCAAGA[C/T]GACATGCAATTTTAA | 64326 |
rs558185084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175989607 | CTAACAGCCAGAAAA[C/T]AAAGGAAAAGGAATC | 64326 |
rs558186865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176069049 | AAAAATTAGCCAGGC[A/G]TGGTGGCACGTGCTT | 64326 |
rs558192526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176186599 | TGTGTTAAAGACTTC[A/G]GCTTTTAAGTTGAGT | 64326 |
rs558214730 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176032789 | AAGCCTGGAACAAGG[C/T]AGGTGAAGGGGAACT | 64326 |
rs558215071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176075083 | CTGAATCCAAGTAAC[A/G]CGTCTGGCCTGTTCA | 64326 |
rs558233387 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175986709 | ATGGTTATAACTGAG[A/G]TATGCACTAAATGCT | 64326 |
rs558257715 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176171904 | GGTATTGAATAAAAA[A/G]CTTACTTATATATTT | 64326 |
rs558266602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176040492 | CAGGTAATTTTTAAA[A/G]TTTTTTGTAGAGACA | 64326 |
rs558268467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175950975 | AATCTGGATGGCGCT[A/G]TGGGTCACACCTGTA | 64326 |
rs558326992 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | RFWD2 | GRCh38.p7 | 1:176006868 | CTTTGTGGCGTTCTC[C/T]GTATTTCCTGAATCT | 64326 |
rs558330311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176009110 | ACAGCTAGGTACACG[C/T]CAGAGCTTCTTGACC | 64326 |
rs558330379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176005004 | TTTTTGGTTGGTAAG[C/T]TATTGATTCTTGCCA | 64326 |
rs558384845 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176197987 | AAAGCATAAACACTG[A/C]TAAGAGAAATTACAG | 64326 |
rs558395142 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176110074 | CATTTACTCTTTTCT[A/T]GACTGCCTGTCTGTC | 64326 |
rs558398252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176107722 | CAGTGAAATCTGGCA[A/G]CCACCATTTTAATCG | 64326 |
rs558416770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175947962 | ATTGATGTAAAACCT[A/G]CCAACATCCTTGGCA | 64326 |
rs558421046 | in-del | -/T | 0.270892 | 0.249126 | intron-variant | RFWD2 | GRCh38.p7 | 1:176070335 | GCCACTTGTGCTGCC[-/T]TTTTTTTTTTTTTTT | 64326 |
rs558424780 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175973922 | AAAAACCCAGCATTC[A/G]GTGTTTGAGGATCCT | 64326 |
rs558432859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176185207 | AAAACAAACTATACA[C/T]ATTAAACCCACAATA | 64326 |
rs558433098 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176192746 | TTACAGTATAAGAAA[A/C]TATGAACAGGGTACC | 64326 |
rs558446410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175981046 | ACAGAATATATATAC[A/G]TTCCCTTACCTAACT | 64326 |
rs558451616 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175961909 | ACATGGAATAAATTT[G/T]AAAAAAAAAAATGGT | 64326 |
rs558457965 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176008737 | AGCTTTTTGCTATTG[C/G]CGGTGTTGCTGTTTG | 64326 |
rs558460836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176020025 | CAAAGGTAAAGATCC[C/T]GTTTAAAACTTCATA | 64326 |
rs558486725 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176012590 | AGGTCTTCATATTCA[C/T]TCACCACTCATTAAC | 64326 |
rs558511485 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:175973492 | GCAGAGCTACAAGTT[A/G]CTAAATGTTACACAT | 64326 |
rs558524872 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176195340 | CACGAAGCAAAAGCT[C/G]AGAAAACTAAAAGGA | 64326 |
rs558533517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176040463 | CTGAGACTACCTGTG[C/T]GCACCACCACGCCCA | 64326 |
rs558546889 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176016428 | AGATCAAATGAAATA[A/C]GGGCTTGAATTTAGT | 64326 |
rs558562670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176091641 | GATACTCTGCTTAGA[C/T]GATAAGTGTGAATAA | 64326 |
rs558568088 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176010585 | CAAATACTATAAAGG[A/T]GATGGTCCTTTCTAT | 64326 |
rs558570630 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176187223 | TCGACCTCTTGGGCT[C/T]GGGACATCTCTCCTG | 64326 |
rs558573040 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176203405 | AAACGTATACTTCTG[C/T]TGCAAGAATGGCTGG | 64326 |
rs558584520 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175970437 | GTTAGAAAACAGAAA[C/T]AAAGTTAGATGGATA | 64326 |
rs558593401 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176065679 | TTTCCCCCACTCCAC[C/T]TCCTGTACCAGGAAG | 64326 |
rs558603408 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176179221 | CTTGACCCTGGGGGG[C/T]AGAGGTTGCAGTGAG | 64326 |
rs558611606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176051767 | GTAGGCCTAGGCTAA[C/T]ACATGTGTTTGTGTC | 64326 |
rs558616353 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175974644 | GAAGAGATTATGAGA[A/C]AGAATCAAAGAGAAA | 64326 |
rs558639244 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176175828 | GCTTACCACTAAGGT[A/G]GGTTTTCTGAATAAA | 64326 |
rs558640747 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176193573 | TTTTAAAATAACTTT[A/G]AATATTATGTTATTT | 64326 |
rs558659269 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176056975 | ATCCTACTCATCATA[C/T]TCACTGTCTCACAAT | 64326 |
rs558659901 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176120369 | AGGTTGCAGTGAGCC[A/G]AGATCACACCACTGC | 64326 |
rs558676888 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176099294 | TGCAGGACTCATGAA[G/T]AACTAAAATGTTGAT | 64326 |
rs558684355 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175992054 | GTAGTATACGTAATC[A/G]TATGTGCTAGACTTT | 64326 |
rs558690741 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:176003860 | GTTCCATATGAACTT[C/G]AAAGTAGTTTTTTCC | 64326 |
rs558700710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176050193 | CTGTTAAAAGAGTGA[C/T]TTATATCAACAGCTG | 64326 |
rs558704616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176177202 | GCTAGAGAACTGTGA[C/T]TACAGAAAATTTTCC | 64326 |
rs558714551 | snp | C/T | | | intron-variant, utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175967564 | AGAAGTTAGGGGAGG[C/T]AGGTGGGAGCAACCT | 64326 |
rs558732400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176030654 | ATATTAGAATTCAAT[A/G]TAACTGTCTGAGCTA | 64326 |
rs558741777 | snp | C/G | | | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175969478 | ATCTCTGGAGACAGA[C/G]ACACAGAGAAGAAGC | 64326 |
rs558749539 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176094783 | TTTATGGTCAGCCTG[G/T]AAATTATGAAAAATC | 64326 |
rs558750679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175971688 | TCAGTCAATGTTTAA[C/T]GGAATTTGGCTGTAA | 64326 |
rs558755157 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176077183 | TGATAAAAGAAAACT[G/T]TGGGCAAATATCCCT | 64326 |
rs558761139 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | RFWD2 | GRCh38.p7 | 1:176188864 | ACACACACACAGACA[C/G]AGAACAAAGCATCCC | 64326 |
rs558768496 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175993679 | TGAAATGAAGCGAGA[A/T]GGGAAGTTTAGAGAA | 64326 |
rs558774904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176086566 | AAATTGTTAGAAAAT[A/G]ATTATCAAATAGAAA | 64326 |
rs558786649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176106092 | CTGGACTGTGGTGGC[A/G]TGTGCTCAGCTCACT | 64326 |
rs558814920 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176020538 | GAAAGATTAGCCAGG[C/T]GAGGTAGTGCATGCC | 64326 |
rs558816391 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176014493 | CCTCAAAACAGGTGG[C/T]TACATTCTGTAATTA | 64326 |
rs558821151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176147371 | AATCAAAGTAGTAGA[C/T]AAACGTTTACAATTT | 64326 |
rs558824606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176189392 | TATGTTTCTTTTTCC[A/G]TTGGGAATTCTTTGT | 64326 |
rs558829931 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176195895 | CCAAAATCGGGGACG[A/G]AGGGGGTTAGGAGCT | 64326 |
rs558830432 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176182320 | CTTGACAAAGGTTAG[C/G]TAAGTTTCAGAACCA | 64326 |
rs558834741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175963023 | TGAAAAACATGAATG[C/T]TACATGTGGGTGTTT | 64326 |
rs558885685 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176066471 | TGGGCAAAGACTTTG[A/C]CCATTTTATCCTAAT | 64326 |
rs558887855 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176057970 | TGGGATATGAGGAGC[A/G]TCTCTGCCTGGCCGC | 64326 |
rs558889467 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175958594 | TATTAAACAAAATCA[A/G]AATATAACCCTTCTT | 64326 |
rs558902926 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176078054 | AAGAATCGATATTGC[C/T]AAAATGGCAATATTG | 64326 |
rs558918232 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176151877 | ACAGGTTTAGTTAGC[A/G]TAAGTTCATCTTCCC | 64326 |
rs558922662 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | RFWD2 | GRCh38.p7 | 1:176058678 | TGTTCACTTGTTTAT[C/T]TGCTGACCTTCCCTC | 64326 |
rs558933535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176147822 | GAAAGGAATTCTCCA[C/T]TATCTCTCCAGAAAT | 64326 |
rs558943676 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176099858 | AAGTTTATTTTGAGA[C/T]GTTAAGAGAGCAGGA | 64326 |
rs558963197 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175962345 | TTACCAAAGATGAGA[A/T]GGTACTGAGAAAAAA | 64326 |
rs558964960 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176080956 | CTTATGAGAAGGATA[C/T]TATCAATTATTCCAC | 64326 |
rs558984024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176189930 | AAGAAAGAATTATTT[C/T]AAAAGGGAGGTTAAA | 64326 |
rs558987350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176181066 | TCTCTACGTTATGTA[A/G]AAGTCAGATTTCTTA | 64326 |
rs558990678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176007997 | TAGCAATCAGGGAGA[C/T]TCCGTGGGCGTAGGA | 64326 |
rs559001334 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175982576 | TAATTGTTTATGTTA[C/T]TGGTAAGATTTTCAG | 64326 |
rs559011554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175975250 | CTTTAAACAATTTAC[C/T]AATATTATCCCCCAC | 64326 |
rs559015066 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176140413 | GGCAAGAAATATTAA[A/T]AAGAAAAAAGTTTGG | 64326 |
rs559020309 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:176053465 | TTCTTAAAAATTATT[C/T]CTTGCCTAATTGTTA | 64326 |
rs559024794 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176201007 | AAAAACATTTTATTT[C/G]GTATACAGGTTGAAT | 64326 |
rs559025584 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175954796 | AAATAAAATTACCAA[C/T]TACTTTTATAAACAG | 64326 |
rs559044260 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176183064 | CTGTTATCATTTTAA[C/T]ACTTTATTTTATAAG | 64326 |
rs559047951 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176100761 | TATCCACCAGTTATC[G/T]GGGGTGTCACAAGAT | 64326 |
rs559061149 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176112150 | GAAGATATTTACGTA[C/G]TGTCTCAGTGCACTA | 64326 |
rs559071344 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176103550 | ACCAACTGAGCACCC[C/G]TAATCTGAAAATCCA | 64326 |
rs559074684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176001066 | TTTAGTCAATTGTCT[C/T]TCAAACCCTTTCCAG | 64326 |
rs559084384 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175987604 | ATTATTCTATTAATG[C/G]TCTATGAACTGTATT | 64326 |
rs559092026 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175999075 | TTGTGGACAGTTTTC[A/C]ACCCATGATGGTATG | 64326 |
rs559107718 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175985551 | TAATCACCCATACAA[C/T]GTCAGGCACTGAGCT | 64326 |
rs559125596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176177554 | GGGAAATGTTTTCTT[C/T]GTAGATGTCTTTAAT | 64326 |
rs559130749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176014374 | TAATCATTTATTATT[C/T]CAACAGCACAAGTTA | 64326 |
rs559131160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176175482 | TTCTCATAAGGAGCG[C/T]GCAACTTAGATCCCT | 64326 |
rs559132128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176204454 | AGCCAAACGGGGGGA[A/G]AAAAAAAGAAAAAAA | 64326 |
rs559147666 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175985532 | GTGGGGACTTAAAAC[A/T]AAGTAATCACCCATA | 64326 |
rs559161261 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176050957 | ATGAACATATACACA[G/T]GCAAAATAAGAATAA | 64326 |
rs559162137 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175998949 | ACTCATGTTAATGAT[A/G]AAGATATGCTCCAGT | 64326 |
rs559164311 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:176037036 | AGGAAATTAAATTCT[C/T]AGTTAAAACCTTCAA | 64326 |
rs559179340 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176143723 | AATGCAGAACCTTCA[C/G]TGATATAACTAAGAT | 64326 |
rs559184980 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176142865 | AATTAGGTACAGATT[-/A]AAAAATAAGAAACTA | 64326 |
rs559185687 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | RFWD2 | GRCh38.p7 | 1:176011692 | CACATAGACATTTAT[C/T]ATAATGCACTTATAT | 64326 |
rs559195537 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175991719 | AAAAAATTAAAATAG[C/G]AAAAAGCTTTTTAAA | 64326 |
rs559199776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176046083 | TAGTGTTCACCATGA[A/G]TAAAAAGTGTCATGC | 64326 |
rs559210728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176133774 | AAACAGAGAGGAAAA[A/G]GACAATGGGAATGAA | 64326 |
rs559242585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176075134 | CCTAGCCTGCACTAC[A/G]TTATCAATGATTTTT | 64326 |
rs559244780 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176081487 | TTCTTTGAAAGATAC[C/T]GTCTCTTTCCACTGT | 64326 |
rs559261196 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175959409 | TCAACGATGCCAGAT[A/C]CCATTACTTTTATTT | 64326 |
rs559264962 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176115617 | AGCTGGGCGTGGTGG[C/T]GCGTGCCTGTAGTCC | 64326 |
rs559284875 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176177012 | GGAAATATATATTTA[A/G]AAGGGTGTTTAATAC | 64326 |
rs559301097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175994709 | ACTATGCTAAATATA[C/T]ATGCACCCAATACAG | 64326 |
rs559302218 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176151104 | CCACCACTAAAAATG[-/A]AAGTCCAAGAAGTCA | 64326 |
rs559320540 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176133189 | ACATACGTATATACG[G/T]ACGTATATGTACGTA | 64326 |
rs559332124 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176067962 | GGCACCAAAGAAACA[A/C]GCCACACCCCCATCG | 64326 |
rs559345646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176171051 | AATGGCATGATCCCA[A/G]CAGGTGGAGCTTGCA | 64326 |
rs559351954 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176045348 | AGCTCACCAATTATC[G/T]ATATAGTATTTTTAT | 64326 |
rs559356736 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176088567 | TTTATATGTGTTTTA[C/G]CTCCATTTCAAAGAA | 64326 |
rs559385584 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176007106 | CATTCATCTTCCATC[A/G]CTGATACCCTTTCTT | 64326 |
rs559402052 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175957938 | ATTACATACTGTATC[A/T]TTCCTGTTATATGAA | 64326 |
rs559412431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176037802 | TTAAATTGACACAGG[C/T]GCCTACTAAAAGCCT | 64326 |
rs559424534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176000587 | TATGTGGTCTCTCAC[C/T]GATTGAAATGTCATT | 64326 |
rs559431700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176122982 | ACCAACAAGACTGAT[C/T]TGACTCCAACAAAAT | 64326 |
rs559444350 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176170169 | TACTGAAGTCTTGAA[C/G]CCTTCAAAGTCATCC | 64326 |
rs559454069 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176170471 | TACTCTCCTTTGTAC[A/G]TCTGTATCAGAGCTC | 64326 |
rs559460042 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175949833 | ATGCAGAGACCTGGT[-/G]AAGATGAGGATTCAC | 64326 |
rs559462964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176018352 | GGAAGTCTCAGTTAT[A/G]TTATGTACATTTTCC | 64326 |
rs559487778 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175984444 | AGGATGTATGGAAAC[A/G]CCTGGCTATCCAGGC | 64326 |
rs559518657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176189283 | TTGTTACTGCATTTA[C/T]TTCTTTCAGTCCATT | 64326 |
rs559521954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176135622 | TAATGACTTAGACTC[C/T]AATTTTTGATCAGTA | 64326 |
rs559528554 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176146288 | ACATGTTCATTTAAA[C/T]ATATATAACTAACAA | 64326 |
rs559531313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176052874 | GTATTTTGACCATCA[C/T]TTCATATCAGCACAT | 64326 |
rs559539028 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175979565 | AAGGGAGAACATAAT[A/G]TAAATGTAATAAAAA | 64326 |
rs559552471 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | RFWD2 | GRCh38.p7 | 1:175994268 | ATGGAAAGGAACAAC[C/T]CATACCAGCCACTGC | 64326 |
rs559554153 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175947431 | GCTGGAGTGCAATGG[C/T]GCGATCTTGGCTCAC | 64326 |
rs559556257 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176165512 | CCAGCCTGGCCAACA[C/T]GGCAAAACCCTGCCT | 64326 |
rs559566029 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176117953 | TATATTCTTTCTACC[C/T]TATAAAATTTAAGCA | 64326 |
rs559577904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176017195 | TTATTAATGAGGCAA[C/T]GTTTTAAAATACAGA | 64326 |
rs559602560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176156714 | AACATATCCATTTCA[C/T]AATAATAATAAAGGA | 64326 |
rs559606574 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176058155 | GGGGGGTCAGCCCCC[A/G]CCCGGCCAGCCGCCC | 64326 |
rs559617962 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176158523 | ATTTAACCACAATTA[A/G]TAACAACGTATTGTG | 64326 |
rs559631087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175948545 | TTAGAAAAGTTACTT[C/T]AGCTAAGCTGAGTTA | 64326 |
rs559634334 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176175485 | TCATAAGGAGCGTGC[A/C]ACTTAGATCCCTTGC | 64326 |
rs559639071 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175951142 | TAATCCCAGCTACTT[A/G]GGAGGCTGAGACAGG | 64326 |
rs559667440 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176023979 | AAGAAAACTACAGGC[C/G]GGGCATGGTAGCTCA | 64326 |
rs559682941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176028430 | GTTAGCTGGGCATGG[C/T]GGTGCAGGCCTGTAG | 64326 |
rs559690806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176032898 | TCATTTAAATTCAGG[A/G]GAGAATATACTTAGT | 64326 |
rs559690814 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176164880 | CACTAGGCTAGGAAG[C/G]CACTTTATAGACAAT | 64326 |
rs559706165 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176152841 | TAACATTTCACAAAC[A/G]GGAGTCATCATCCCA | 64326 |
rs559727195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175971870 | GGATTTAGTCTCTAC[A/G]TCTTCCAAAGTGACC | 64326 |
rs559727430 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176102448 | GTCTCTGTCCAAAGT[A/T]CTGAAACTGCCACTG | 64326 |
rs559747881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176160607 | CCCATCGAAAAGTGG[A/G]CAAAGGATATGAACA | 64326 |
rs559760029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176152855 | CAGGAGTCATCATCC[C/T]ATACTTTAGATAGGA | 64326 |
rs559766960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176113563 | AAAGTAGTGTTAATA[C/T]AAATGGTAACTGTGG | 64326 |
rs559769580 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175945988 | GATCCTATGAGAACC[C/T]ATGTAGTTTTGAGCT | 64326 |
rs559775485 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175947661 | AGGCGTGAGCCACTG[C/T]GCCCAGTCGAAGAGA | 64326 |
rs559784277 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176015968 | AGTAGAACACACATG[C/T]TTCAATTTAACGTGA | 64326 |
rs559786029 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176209069 | GGGCAACAGAGCAAG[A/G]CTCCATCTCAAAAAA | 64326 |
rs559803046 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176169917 | CTCTTGCTGCTTTAT[C/G]AACTAAGTTTATGTA | 64326 |
rs559818125 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176204811 | GTGCCTGTAATCCCA[A/G]CTACTACTCGGGAGG | 64326 |
rs559833216 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176196247 | GTTAGCAGAAGAAAT[G/T]TATAAAGTAAACTGA | 64326 |
rs559869395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176149645 | AAGTGGACAGCTTGC[A/G]GGTAGGGAGTAACTC | 64326 |
rs559883554 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176202468 | GGCTGGGATTACAGG[C/G/T]GTGAACCAAGGTGCC | 64326 |
rs559889966 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176101716 | ACTTATTTTGTTTTG[A/T]TACATGTTTTCTAAT | 64326 |
rs559895080 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176062647 | AGGTATTCACCCAAA[G/T]AAATAAATATAAACA | 64326 |
rs559919718 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176182887 | AAAGTAAAATGACTT[A/T]AAAAAATAGTAAAAG | 64326 |
rs559926909 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176095170 | AACTTTATAAGTTCA[A/C]GGAATACATACAAAA | 64326 |
rs559927200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176057017 | CTCCAAAAATATTTA[C/T]ACTTCTCATCCTTAT | 64326 |
rs559928994 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176049578 | ACAAACAGGTCCCCC[C/G]CCTCAAACCACCTTT | 64326 |
rs559938614 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176009425 | TAATAATATACTAAC[A/G]TATTCTCATGTTAAT | 64326 |
rs559947346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175977523 | CTGATAGCTTTATTT[A/G]GGAAACTGGTGAATA | 64326 |
rs559950149 | in-del | -/ATG | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176185154 | CAATGCTTGTAGGTA[-/ATG]ATGACAACAATCATA | 64326 |
rs559954107 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176124552 | CCTAGCTTATTTCAC[C/T]TAACATAATAACCTC | 64326 |
rs559969757 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176203059 | GTCAACCTTCTCGGC[A/C]GGGCGCGGTGGCTCA | 64326 |
rs559971333 | in-del | -/A | 0.128288 | 0.218372 | intron-variant | RFWD2 | GRCh38.p7 | 1:176181841 | GCGAGACTCCATCTC[-/A]AAAAAAAAAAACCAA | 64326 |
rs559996100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176153487 | CTTAAGAAGCTTGTC[A/G]GCTGAGACTATGGGA | 64326 |
rs560001630 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176005510 | ATAAATTTCCCTCTA[A/C]ACACTGCTTTGAATG | 64326 |
rs560004258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176055367 | TTAAACCCGGGAAGA[A/G]GAGGTTGCAGTAAGC | 64326 |
rs560031473 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176196005 | ACCTGTGCATGTACA[A/G]GTAAAATAAATTAAA | 64326 |
rs560039196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176117423 | CAGAAGTGTAGACTA[C/T]CTTTTACTTCCTCTA | 64326 |
rs560042031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176056468 | ATACTTACAATTAGA[C/T]TTAAACTTCAGTGCA | 64326 |
rs560054469 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176070630 | CCGCACCACTGCACT[C/G]CAGCCTGAGCAACAG | 64326 |
rs560058901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176107937 | ACTCTTCAAGAATGT[C/T]GATGTCATAAACTGA | 64326 |
rs560068624 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176006573 | CCTCAGCATTTGCTG[C/G]TCTGTAAAGTATTTT | 64326 |
rs560081278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176098601 | ATATGGTTTTTCTGT[A/G]AACTAAGCATTGAAA | 64326 |
rs560084157 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176202521 | GAAAAACAGAGCCAC[G/T]TGTTTTTCAGACTAT | 64326 |
rs560097122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176108530 | ATCTTCCTGGACGAC[C/T]ATCAACTCAACTACC | 64326 |
rs560098231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176139625 | ACCGTGGAATACTGT[A/G]CAGCCATAAAAAGAA | 64326 |
rs560106045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175999113 | AAATGTAGCATCTAA[C/T]AGCAAATAAAAAATT | 64326 |
rs560126176 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176008933 | CCTTAATGCTTTGCA[C/T]GATTTGTGTGTATGT | 64326 |
rs560129338 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176001791 | GGGTAGGTCTCCTGA[A/C]AAAGAACTCACTCGG | 64326 |
rs560129659 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176006900 | AACGTTGGCCTGCCT[G/T]GCTAGATTGGGGAAG | 64326 |
rs560146894 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175974269 | GTGCTTAGACACATA[A/C]CACTGGTTAGATACA | 64326 |
rs560156071 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176098842 | TTCAAAATTGTCTTT[C/T]CTGATGCCTAGCTTT | 64326 |
rs560167404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176013270 | GTATGTAACTCATCC[C/T]AAAAATATATGATTA | 64326 |
rs560167871 | snp | C/T | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992711 | GGGCACCTGCCATTG[C/T]CCAGGCTTGCTTAGG | 64326 |
rs560176827 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175987774 | AGGCATTAGATGTAT[A/C]AGAGCATTTGAATAA | 64326 |
rs560176999 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176111108 | AGTAAGCTGAGATGG[C/T]GCCACTGCACTCCAG | 64326 |
rs560184888 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176109408 | CACCACTGATCTACA[G/T]GACCACCTTTATCAC | 64326 |
rs560189047 | snp | A/G | | | intron-variant, utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175971180 | GATAAAGCCAGAAGG[A/G]AATAAGGATGTTAAT | 64326 |
rs560198084 | in-del | -/AAC | 0.00636936 | 0.0560724 | intron-variant | RFWD2 | GRCh38.p7 | 1:175972116 | AATTATGTAACCCAT[-/AAC]AACAACAACAACAAC | 64326 |
rs560208685 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175967675 | AGCAGCTTTCCTCTG[A/C]AAATGGTTATTTCTG | 64326 |
rs560221227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176110130 | TTCACACAATGCAGA[C/T]GATACTATTTATCTT | 64326 |
rs560221292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176193041 | CAAACAGTGAAAATA[C/T]GGATGACAACTTTCC | 64326 |
rs560226640 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175944986 | TCCCAATGTCCCAAA[G/T]GTCATAAAGGAGGGA | 64326 |
rs560227409 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176035004 | GGACCCAACATCTTA[A/C]AATATAATATTCAAA | 64326 |
rs560237737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175981617 | TGAAAAATTTTTTGG[C/T]TAAAACTGCAAAAGC | 64326 |
rs560240501 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176022254 | AAGATCTAAGCAAGA[C/T]AGACAGGGAAGCTTA | 64326 |
rs560256966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176151998 | AAGCAGAATGGCATA[C/T]GCAAGTTATTTAGAA | 64326 |
rs560261862 | snp | A/G | 2.64624e-05 | 0.00363737 | intron-variant | RFWD2 | GRCh38.p7 | 1:175987148 | AGAATAGAAAAACTC[A/G]GAATTAGGACATCAC | 64326 |
rs560313783 | in-del | -/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175950403 | GCTTAAGATAAATTA[-/T]TTTTTTTTTTGCATG | 64326 |
rs560334308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176131140 | AAAACAATAGGCTGG[A/G]GCTAGGCAATTACGG | 64326 |
rs560339144 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176034636 | GGAGAAACCTGGAAA[C/G]AAAGTAATGGAGAAG | 64326 |
rs560358647 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176019077 | AGGCTGAGGCACGAG[A/T]ATCGCTTGAACCTGG | 64326 |
rs560371096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176021462 | CATTGATTTGCTTTA[C/T]ATTAATCTCTTTTTT | 64326 |
rs560372710 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | RFWD2 | GRCh38.p7 | 1:175995006 | GGAAGTAAAGCTCTC[C/T]TCAGCAAATGCAAAA | 64326 |
rs560385393 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176063360 | CCACCGCGCCTGGCC[C/T]GAAAATGTTTTATGT | 64326 |
rs560386242 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175974066 | TTAGATCTTATTCTG[C/T]AACCATTGGGGAAAC | 64326 |
rs560402853 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176008021 | CGTAGGACCCTCGGA[C/G]CCAGGTGCGGGATAT | 64326 |
rs560404724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176003255 | CTGGATATTAGCCCT[C/T]TGTCAGATGAGTAGG | 64326 |
rs560410402 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176137472 | ATTTAAATTCCTAAC[G/T]CCAGGATGCGGTTGT | 64326 |
rs560415867 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176198178 | AATGCAAAGAACATA[A/C]ATAATCAAAACAACT | 64326 |
rs560417306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176099348 | AACTAAATGAACTGA[A/G]CTCACCAAAAACTGA | 64326 |
rs560418351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175974802 | CTTTGGAAGGCTGAG[A/G]CAGGTGGATCACCTG | 64326 |
rs560419968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176010998 | GGCTAATTTTTAATT[A/G]TGAGGAACAGTGAAA | 64326 |
rs560436952 | in-del | -/TG | 0.00994209 | 0.0698011 | intron-variant | RFWD2 | GRCh38.p7 | 1:176052190 | ATACACAAATACCAT[-/TG]TGTTAAAGCTACCTA | 64326 |
rs560439124 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175955495 | AGGTACAACCCAGTG[C/T]GACAGTCAAGAAAAG | 64326 |
rs560440700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176013816 | AAAATTCCAGACTTA[C/T]TTAAATACGTGCACA | 64326 |
rs560447463 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175948464 | GTAGGATAGGATCTA[C/T]CTAAATATCCTTCAG | 64326 |
rs560448081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175982144 | AAATACAGAATGGCA[A/G]TATGACCTAGCAATT | 64326 |
rs560448445 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175952348 | AATCGCTTGAACCTG[C/G]GAGGCAGAGGTTGCA | 64326 |
rs560448696 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176011806 | TCACCTAGAGACTTT[C/G]TGCCTATTAGTAACT | 64326 |
rs560449359 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175976545 | AGTTTCCCAAAGTGC[C/T]GGAATTACAGGCTTG | 64326 |
rs560458391 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176199713 | TAATATGAAATTCCA[C/G]AAAAGGCAAAATGAC | 64326 |
rs560458991 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176111726 | TGTTCATACTTTTGG[G/T]TTTTTTTCAGTTTTA | 64326 |
rs560459756 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176078493 | CCATATACAATAACT[C/G]AAGATCAATCAAAAC | 64326 |
rs560465402 | in-del | -/AGAA | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176031771 | AATGTGTAAAGTGTC[-/AGAA]TTCTAAGTGTCACCT | 64326 |
rs560468029 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176105546 | GTGTATTTTGATCGT[G/T]ACAGCTAGGTTTCCA | 64326 |
rs560475010 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176076492 | AGAGAGGAAAATTTA[C/T]AGCACTAAAAATGCC | 64326 |
rs560475937 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176007453 | AGTTTTTCTGTTCTG[C/T]TTTTTTCCCATCTTT | 64326 |
rs560484098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176061618 | GCAGCAAGAGTGAAA[C/T]TCCGTCTCAAAATAA | 64326 |
rs560484111 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176054315 | TACAGGCGTGCACCA[A/C]CATGCCCAGCTAATT | 64326 |
rs560493325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176054854 | TGCTTTCCTAATACC[A/G]TAACTTTACAAAAAA | 64326 |
rs560493626 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176051778 | CTAATACATGTGTTT[A/G]TGTCTCAGATTTTAA | 64326 |
rs560502877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176004685 | ATTGAACCAGCCTTG[C/T]ATCCCAGGGATGAAG | 64326 |
rs560517019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176118959 | TAAAGTTAGATGAGT[A/G]CCAAAAAATGCAGCA | 64326 |
rs560531923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992513 | AAAGGAGTGACAGAC[A/G]GCACCTGGAAAATTG | 64326 |
rs560537115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176101113 | AGGGGACATAAGGTG[C/T]ACATGGGTAAGAGTG | 64326 |
rs560561247 | snp | A/G | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176159182 | AGTAATATACAAAAT[A/G]CAAGCACACACACAT | 64326 |
rs560568940 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176172976 | TATAATCCCACTGAA[A/T]GCTGCACTAGAGATC | 64326 |
rs560572759 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176047127 | TGGAAATCTAATTAG[A/C]CCAAAGGTAGTAAAA | 64326 |
rs560575754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176048128 | AGACACACATTGATA[C/T]GCCCACTTTTCTTTA | 64326 |
rs560583731 | snp | C/G | | | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176208754 | GGAAGTTGCTGGGCA[C/G]ATGTTTTTGCGGAAG | 64326 |
rs560586920 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176108238 | TATAAAGTTCATACA[C/T]TTCTGGCTTCACTTA | 64326 |
rs560593515 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176201943 | GTTTATTCCAGTAAC[G/T]GAACATGCTTTTAAC | 64326 |
rs560608194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176197446 | GAAACAGGCCTCAGA[A/G]GAAACCGAATCTGCC | 64326 |
rs560616506 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176151315 | AAGAAAGGAGAGAAA[G/T]AAAGAAGGAAAGAAA | 64326 |
rs560623462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176082308 | ACACAACTTTTTCAA[A/G]GTAAATGTTCATGAT | 64326 |
rs560637153 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176127154 | TGATCCTTGCATACA[C/T]TGTGAAATGATCAGA | 64326 |
rs560645347 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | RFWD2 | GRCh38.p7 | 1:176142989 | CCAAAGAAAGCAGGA[C/T]GGAAATAATAAAGAA | 64326 |
rs560650549 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176006219 | GATCTTCCTCCATCC[-/T]TTTATTTTGAGCCTA | 64326 |
rs560651018 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175980677 | TGTCCACCCTAATGA[A/C]CACTGCTTTTTTTTT | 64326 |
rs560652270 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176179198 | AGTAGGCCGAGGCAG[A/G]AAAATTGCTTGACCC | 64326 |
rs560652549 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176100290 | GCTACTTGGGAGGGT[G/T]AGGCAGGAGAATCGC | 64326 |
rs560658146 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176130370 | AATCTCTAATTTTCT[C/T]ATTATTTCACACACA | 64326 |
rs560659006 | snp | A/C | 5.89675e-05 | 0.00542957 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176206736 | CAGGCCCGTGGACAC[A/C]GCCCCGCCGCCGCTA | 64326 |
rs560677023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176008785 | TGGGACTAAATCTGT[C/T]CAGCCTGTAATTCCT | 64326 |
rs560687171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176141449 | CAGGTTGCAGTGAGG[C/T]GAGATAGTGCCACTG | 64326 |
rs560708835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176083162 | ATGATTCTTTTTATA[C/T]GGAATCCTATTACTG | 64326 |
rs560709185 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176075934 | CTTGAACCTGGGAGG[C/T]GGAGGTTGCAGTGAG | 64326 |
rs560711676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176093467 | TACTCCCAGCAGTTT[C/T]GGTGGCTGAGGTGGG | 64326 |
rs560722409 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176031047 | AATGACCATCAATAA[A/C]CAGAAATTAGGAAGG | 64326 |
rs560723177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176183537 | GCCCCTATAGAAAAC[A/G]GTATGGCAGTTTCTC | 64326 |
rs560740539 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176000432 | TATACTTTTATTTAA[C/T]TGGGAGCATAGAATT | 64326 |
rs560758186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175966795 | TTTATATATCTCCCT[A/G]TAAGTATTATTTCAA | 64326 |
rs560760248 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175959330 | GTATGTATCTACAAA[A/T]CTCTTACAGCAGACA | 64326 |
rs560761260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176124029 | CATGAACACTGCAGT[C/T]TGGCTTCTTCACACC | 64326 |
rs560762647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176120701 | CTTCAAAAGCAAAGA[C/T]GTATTTCCTAACTAG | 64326 |
rs560764541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176127684 | ACTTAGGTTGTTTGC[A/G]TGGCTACTGTGAATA | 64326 |
rs560765268 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176041446 | TCTGCCTCCTAGGTT[C/T]GAACAATTCTTGTGC | 64326 |
rs560790592 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176185371 | AAATTCAGGTCTACG[G/T]TCTTAACCACTTGTC | 64326 |
rs560792737 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176133618 | ACCTAGAATAGTCCC[C/T]AGCACATCAGAGGCA | 64326 |
rs560811486 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176065798 | CTGCAACCTCCACCC[C/G]CTGGGTTCAAGCAAT | 64326 |
rs560836262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176148800 | CTTACTGATAACTTT[C/T]CAGCACATCTCCACA | 64326 |
rs560870597 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176087285 | AACTAAAGAGCTTCT[G/T]CAAAGCAAAAGAAAC | 64326 |
rs560876140 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176126893 | TAATCATAATTACTA[C/T]AGTTTTTGGAACAGT | 64326 |
rs560881244 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176052078 | TTACATTCATTCACC[A/T]CTCACTCACTGACTC | 64326 |
rs560893151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176038590 | TTTGGGAGGCCAAGG[C/T]GGGCAGATCACAAGG | 64326 |
rs560901202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175963403 | ATCTGCGCCTTTGTT[C/T]ACACTGTTCTCTAGC | 64326 |
rs560902421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176085596 | ATATAGAACAAAAAA[C/T]AGTCATTGGAAAGTA | 64326 |
rs560915091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175954847 | ATACAAGTAAAGATA[A/G]TTCAGTCATATACAA | 64326 |
rs560923415 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176124158 | GCAGGTGTATATACT[C/T]ATGAGGTACAAGAGA | 64326 |
rs560930744 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175954732 | CTAAGGAACATTTCC[A/G]AACTCAGCTTGTAAA | 64326 |
rs560934010 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175994635 | AACCAACAAAGATCA[A/G]AACAGACAAAGAAGG | 64326 |
rs560942958 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175965662 | GGTGCAGTCTCGGCT[C/T]ACTGCAACCTCCGCT | 64326 |
rs560946437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176155955 | AAAAGGGAAATCAGC[C/T]AGATGGATGCGAGAA | 64326 |
rs560952875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176057649 | GTGCTCAATGGTGCC[C/T]AGGCTGGAGTGCAGT | 64326 |
rs560965662 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176094121 | CAATAATCAGGAACA[C/G]GGCATATAAAACAAA | 64326 |
rs560978630 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176204853 | GAATTGCTTGAACCC[G/T]GGAGGCGGGGGTGGC | 64326 |
rs560981504 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176205075 | ATTCCTTATTCCTCA[C/T]ATCTTTTACTTTATT | 64326 |
rs560989261 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176077967 | ATCTCTACAATGAGA[A/G]CACAAAGCCCTGCTG | 64326 |
rs560990818 | in-del | -/TTC | | | intron-variant, cds-indel | RFWD2 | GRCh38.p7 | 1:175967873 | AATAATATTTCTTTT[-/TTC]TTTTTTTTTTGAGAT | 64326 |
rs560996376 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176122003 | AAATTAGCCGGGCAT[A/G]GTGGCGGGCGCCTGT | 64326 |
rs561000084 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175976580 | ACTGTGCCCGGCCTC[A/T]TTTATTCCTTCTTAT | 64326 |
rs561018698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176015933 | ATATGATTTTTTTAA[A/G]AAGAGGATGACATTT | 64326 |
rs561032761 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176112146 | ATGAGAAGATATTTA[C/T]GTACTGTCTCAGTGC | 64326 |
rs561039943 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:175961602 | TTGGGAGGCTGAGGC[A/G]GGAGGATCACCTGAG | 64326 |
rs561051152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176176386 | CTTAATACTCAGTTC[A/G]TTGAAATAAAAAAGA | 64326 |
rs561052378 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175962527 | ATAAAAACCTCCAAA[A/C/T]CGAGCCTTTTCATTG | 64326 |
rs561055089 | snp | G/T | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176134804 | GTGAATTCATAACAT[G/T]ATAGTATTCTACTCG | 64326 |
rs561059486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175969986 | ATGAAATTGATAAAA[A/G]TAGGCTCTCTGGGTT | 64326 |
rs561069977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176195477 | AACCAACTTTACTAT[C/T]TGACATGTATAGAAC | 64326 |
rs561081541 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176008456 | TTTCAACAACAGAAT[C/T]ATTTGTTTTTATTTC | 64326 |
rs561105333 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176080158 | ATAAACACAATTTTA[A/T]CTGTCAATTTTAAAA | 64326 |
rs561106473 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175994961 | TTTTCAGCACCACAC[A/C]ACACCTATTCCAAAA | 64326 |
rs561106893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175948634 | TTAAATTTTCCCTTT[C/T]ATTTCTAATAAAGCT | 64326 |
rs561110454 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176072359 | TTTACAGACATAGGA[A/C]TATGCAAGAAATAAG | 64326 |
rs561131029 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175989748 | AAACATTATGGGACA[G/T]CTGGATAAACATAAT | 64326 |
rs561133573 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175994304 | CATGCCAAATTGTAA[A/T]GCCCATCGAGGCTAG | 64326 |
rs561140211 | in-del | -/AAA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176074538 | AACCAGAGGTATCTT[-/AAA]AATTTCTTATATTAG | 64326 |
rs561145765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175990631 | CCTTAAATATCACAG[A/G]TTTTCTTTTCATATA | 64326 |
rs561155457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176201567 | AAAGATAACTGCTTA[C/T]CAACACATTCTTTAG | 64326 |
rs561161206 | in-del | -/ATTT | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176091007 | ACCAAAAGAAAGATA[-/ATTT]ATTTAGGAACAACAA | 64326 |
rs561162848 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175963977 | TATGTGGATTCGTAT[A/G]TAAAATGTTAAAGAT | 64326 |
rs561169244 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176086186 | AAAATGAAGACAGAA[A/T]TCATTATGCCATTCT | 64326 |
rs561171571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176168316 | CCCGTGTCAGACTCT[C/T]AAAGTGCTGGGATTA | 64326 |
rs561199789 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176098491 | AACAAACAAAAAAAG[C/T]TAAAAGTTCAAACAA | 64326 |
rs561210366 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176018398 | GTCTCAGTTAAGAAA[G/T]AGTAGCAGAAACATT | 64326 |
rs561219416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175988983 | AATACACAGTAACAC[A/G]TGAGTTGACTTTAAT | 64326 |
rs561227891 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207455 | GGCCGTCTTAATACA[A/G]TGAAAGAATTGAGGA | 64326 |
rs561249709 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176086751 | CTTCACAGAACTGGC[A/G]AAACTACTTTAAAGT | 64326 |
rs561259500 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:175997684 | CAGAGAAATGTAAAT[C/G]AAAACCACAATGAGA | 64326 |
rs561275467 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176047959 | GGGTTCTTGTCTCCA[A/G]AGACTTGGGAGGCTG | 64326 |
rs561286890 | snp | A/C | | | intron-variant, missense | RFWD2 | GRCh38.p7 | 1:175972004 | AACACTTTGGCACTT[A/C]TAAATTTCCACCGGT | 64326 |
rs561287990 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176064527 | CAACATTAGTTACCA[C/T]ACTCTAATACACCTC | 64326 |
rs561324859 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175998604 | TATAGCATTTCAGGA[C/G]TTCTGCAAATTATGA | 64326 |
rs561344519 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175993508 | TGAAAAAAATTTAGA[A/C]GAATGTATAACTAGA | 64326 |
rs561353759 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176145710 | GGATGAATCTTAACA[C/T]TCAGCCGAAGAAGAT | 64326 |
rs561356705 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175989278 | CAATATTATAGTTTA[C/T]ATACACCCTCAGTGA | 64326 |
rs561360838 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176036636 | GTGAGAATGCAATGT[A/G]CATTCAGTAGGAACC | 64326 |
rs561364606 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176131902 | CTGTTTGCCTATTTT[C/T]CCTTCTTGAACTGCT | 64326 |
rs561382583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176119372 | GAATTCTGTGACTGT[A/G]AGCCTAAAAAATGAA | 64326 |
rs561388354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176075205 | CTGCATTTTCAAATT[C/T]TACTCAGTCAAGTGC | 64326 |
rs561390589 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176130117 | GATAATCAAACCTGG[A/T]CTAAGTATGTTTCAA | 64326 |
rs561395106 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176003923 | GGGGATGGCATTGAA[A/T]CTGTAAATTACCCTG | 64326 |
rs561398913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176071845 | ACCTAATTAATGCTT[A/G]TTTTGTGGATATGTG | 64326 |
rs561411480 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176037067 | ACAAAGAAAACTACA[C/T]GCCCAGAAAGCTTCA | 64326 |
rs561418852 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176080981 | TTCCACTTTAGAGAC[A/G]AAGAAATTTGGCATA | 64326 |
rs561430318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176140590 | CAACCACTTCAAGGA[C/T]GTGGAAAGAAGAAAT | 64326 |
rs561444356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175958642 | AATGTTAAGCATTAC[A/G]TTAAATTGATGACTT | 64326 |
rs561446762 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176042687 | AGTGAGCCGAGACTG[A/C]GCCACTGCACTCCAG | 64326 |
rs561454491 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175959226 | TATATCATGTTAAAT[A/T]GGTACAAAAAAGCAG | 64326 |
rs561459384 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176182589 | TCAATAGTGACAAGG[A/T]TGAGAAAGCCTACTC | 64326 |
rs561475155 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176112463 | TTGTGCATATCTGTG[A/G]GGGGTACATGTAATA | 64326 |
rs561480348 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176078987 | AAAAGTCAAAAAATA[A/G]CAGATACTGGCAAGG | 64326 |
rs561503253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176162684 | ATAAGTTATAATGTA[C/T]TGAAATTGTTCTTTA | 64326 |
rs561507823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176154963 | GATTATTAGACATAA[A/G]GAACAAATCCTTGAA | 64326 |
rs561525482 | in-del | -/AAG | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176156295 | TAAAATTACAATAAA[-/AAG]AAGTACATGAAAAAT | 64326 |
rs561525750 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176172207 | GCTGCATACCAACAC[A/G]CCTGGCTAATTTTTT | 64326 |
rs561526158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176125983 | TTATTTGTGGCTTTA[C/T]AAATAAGAATATATT | 64326 |
rs561538341 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176198274 | AACAGTGTGGCACTT[A/G]TGTAGGGATAAACAT | 64326 |
rs561538685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992257 | TAAAAATGTACAATG[A/G]GAGGTGGAGGCAAGA | 64326 |
rs561554497 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176021842 | TGAAAAAGAGAAGCA[C/T]AAAAAATCATTTTAA | 64326 |
rs561556592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176029509 | GTTGTCATCCTGGAT[A/G]CACATTAGAATAAAT | 64326 |
rs561570860 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176022453 | AAATGATATTTATTA[A/G]TAAGCAACTTCATGA | 64326 |
rs561575336 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176161837 | AACTTATTTTGGCTG[C/G]CTCAACCTGACACAC | 64326 |
rs561586413 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:176183983 | GACGAGTTTCAGTTT[C/T]GCACAAAAAGTTCTA | 64326 |
rs561591535 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:175980765 | AGTGTCCTTTACAAG[C/T]ACTGCCTTTTACTAT | 64326 |
rs561592734 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175948049 | TTTGGGAAAAAGGAC[G/T]ATCTTTCTTTTTAAT | 64326 |
rs561620426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176136244 | ACTGAGCGATTTTTT[C/T]TGTCAGTCTAATCGA | 64326 |
rs561621125 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | RFWD2 | GRCh38.p7 | 1:175946654 | CTTTTTTTATGGCTA[A/G]GCTTCCTTGAATCAC | 64326 |
rs561629718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176075801 | AGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 64326 |
rs561635516 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176168857 | GGCTATAGTGTAGTG[C/T]TTACAGCAGGAAAGA | 64326 |
rs561641163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176088560 | GCTTTTCTTTATATG[C/T]GTTTTACCTCCATTT | 64326 |
rs561664214 | snp | A/G | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176185295 | CACAGTTTATAGATG[A/G]GGGAACAGAAGCAGA | 64326 |
rs561673140 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176119894 | TGAGAAAATTCAGGC[A/C]CTGAGAGATTATATA | 64326 |
rs561674067 | in-del | -/GG/TTGT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176165395 | TGTGTGTGTGTGTGT[-/GG/TTGT]GTGTGTGTGTGTAGG | 64326 |
rs561678070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176205237 | GCACTATCGACTGTG[C/T]AGAAGTGCAAACACT | 64326 |
rs561709508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176110161 | GTCTTAGATTCAACC[A/G]ATTTTTCGAAATTCT | 64326 |
rs561712766 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176017518 | TCATACAGATATCAT[G/T]ACTTTTATTTTTATT | 64326 |
rs561738019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176061643 | AAATAAAAAAAAGAA[A/G]AAGAAAAAGAAAAAA | 64326 |
rs561744309 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176054888 | TTTTCCATAACCTCT[C/T]CTCTCGTTCTCTTTA | 64326 |
rs561754387 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176011944 | TGATAAACAACTGTG[C/T]TACTGGCTTATGTAT | 64326 |
rs561765353 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176160499 | ACCTACAGAATGGGG[-/A]AAAATTTTTGCAATG | 64326 |
rs561771132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176165633 | CCAGGAGGTAGTGAG[C/T]CAAGATCGTGTCACT | 64326 |
rs561780088 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176157692 | CAGGACAAAGTTCAG[C/G]AATATATAAAGGATT | 64326 |
rs561795044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176001719 | CTTTGTGGACTTACA[C/T]TACAGTCTAGTATCC | 64326 |
rs561795129 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176129445 | GCATGACAATTTTTT[A/T]AAAAAAATGAATTAA | 64326 |
rs561798855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175995043 | AAATTATAACAAACT[A/G]TCTCTCAGACCACAG | 64326 |
rs561803532 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175986222 | GACAGGGTTTCACCG[C/T]GTTAGCCAGGATGGT | 64326 |
rs561816225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175966020 | AAACATAGGTTCCAA[C/T]ATCATCTTCAAAGGT | 64326 |
rs561873949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176116308 | ATTGCTTGAGCCTAG[A/G]AGGTCAAGGCTACAG | 64326 |
rs561895339 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176122105 | AGATCGCGCCACTGC[A/G]CTCCAGCTTGGGCGA | 64326 |
rs561904787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176164751 | TCTTTTCCCGTGAAT[C/T]GATACATTTTCCATA | 64326 |
rs561905365 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175955041 | TTGCTTGAGTCCAGG[A/G]GTGTGAGACCAGCCT | 64326 |
rs561913144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176205938 | GTGAAAAATCTGTTA[A/G]CAGACTTTGACTACA | 64326 |
rs561916701 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:176123720 | AAAAGAATTAAAAAT[A/C]TTTACCCCCACCCTG | 64326 |
rs561922040 | in-del | -/AGAA | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176188939 | AGTCACAGATGACAG[-/AGAA]AGAGTTAGGAAAAAA | 64326 |
rs561923417 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176088583 | CTCCATTTCAAAGAA[A/G]GCATAATAAAAAATT | 64326 |
rs561939252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176067447 | GGATGTGCAGAGGAA[C/T]ACATCGGTACAAGAG | 64326 |
rs561939521 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175953317 | AGGAAATGAGGAACA[C/T]AGGAACTTAGAGAAG | 64326 |
rs561948297 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176025935 | TAAAAAAGACACCTA[A/T]TGTAACTGTGGAAAG | 64326 |
rs561952873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176159836 | TGGTGGTCACACTGG[A/G]AGAAGGGAATGAGAT | 64326 |
rs561960017 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176054220 | GCTGGGGTGCAGTGG[A/G]CATGATCTCGGCTCA | 64326 |
rs561971084 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176115679 | ACTTGAACCCAGGAG[A/G]AGGTTGCAGTGAGCC | 64326 |
rs561988948 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992445 | AAGCAGGGTGAGGCA[C/T]TGCCTCACTCGGGAA | 64326 |
rs562003432 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176028247 | TTAAAACCAAGAGAG[C/T]TTAGTTTCAATGTCA | 64326 |
rs562007833 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176110686 | AAAAAAGATGACAAC[A/C]ACCACAAAACCCCAA | 64326 |
rs562008795 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176019153 | CTTGGGCAACAGAGC[G/T]AGAATAGACTTTTTA | 64326 |
rs562017609 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176105194 | GAAAAGCTGAAAGGG[C/T]AGCCGTTATTGATTA | 64326 |
rs562048011 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176170892 | GCACTTTGGGAGGCC[A/G]AGACTGGTGGATCAC | 64326 |
rs562062595 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176057313 | CTTCAAGAATGTGAC[C/T]TCTCCCTCTCCCTCT | 64326 |
rs562071699 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176053523 | TTAATATCCTGGTCT[A/G]TCAGTTTTCTTGACT | 64326 |
rs562097777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176006041 | GTGCCCTTGTATTGG[A/G]TGCATATATATTTAG | 64326 |
rs562104704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176022127 | TAATTTATTCCTTTG[A/G]TAACTATATTGGGAC | 64326 |
rs562113619 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175985389 | ATCTTTTTTCAGAGG[A/T]TTTAAGTTTGCATCC | 64326 |
rs562113835 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175978567 | CACTCTATTCTGGAT[A/G]CTGAGGGAAGAGTGA | 64326 |
rs562138859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176190783 | AACTGTCCAACAAAC[C/T]AATATGTACATAGTT | 64326 |
rs562143431 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176063295 | TCGATCTCCTGACCT[C/T]ATGATCCACCCGCCT | 64326 |
rs562144661 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175949331 | AAAGGAAGATGAATT[G/T]GGGATTTATTTACTC | 64326 |
rs562146822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176144503 | TAAATACACAGTCTC[C/T]CAGATTTATCTAGTC | 64326 |
rs562175762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175965720 | CAGCCTCCTGAGTAG[C/T]TGGGATTACATGTGC | 64326 |
rs562195085 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176118400 | AAAATTACACGAAAG[A/T]AAGAAGTTCTAAGGT | 64326 |
rs562207903 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176203267 | GCGTGAACCCGGGAG[A/G]CGGAGCTTGCAGTGA | 64326 |
rs562217447 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176104547 | AAACCAGTAAACATA[C/T]GAAAACATAGTCAAT | 64326 |
rs562218425 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176108892 | GCAGAGGCAGGCAGA[C/T]CACGAGGTCAAGAGA | 64326 |
rs562220855 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176164323 | CATGGAAGACACTTT[A/T]AGCTAACTATCCAAA | 64326 |
rs562254399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176096003 | GTATGCACTGTACTT[C/T]ATCTGCTAGCAGGAC | 64326 |
rs562256261 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176103129 | GGGAAGGGGAACCCA[C/T]TAGGGTGTTACAGTT | 64326 |
rs562277272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176143808 | TTGATTGACTCCCCA[A/G]TGCTAAACCAAAGTA | 64326 |
rs562294029 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176096490 | CAGCCACTGTCCAGG[A/C]CCCAAGGCGGCCTCA | 64326 |
rs562306115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176147963 | GGAGTGCAGTGGCGC[A/G]ATCTCGGCTCACCAC | 64326 |
rs562310692 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176063442 | ATATAAATTATACTT[A/C]AGTAAAGGTGATTTT | 64326 |
rs562311394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176112606 | TCTGAAATATACAAT[A/G]AAGTAATAACTATAA | 64326 |
rs562334192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176087863 | ACCAACTCAAATGTC[C/T]ATCAATGATAGACTG | 64326 |
rs562347550 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176060517 | TACAACAGAGACTCA[A/G]CAGAGAATCATATGA | 64326 |
rs562350779 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176056511 | ATCATTATAATGGGG[A/C]GTGTGTGTGTGTGTG | 64326 |
rs562364529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, missense | RFWD2 | GRCh38.p7 | 1:175972040 | CAAGATTGGATGTGA[C/T]AGAGATGGGATCTTT | 64326 |
rs562385299 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176009455 | TACAAAAGGGGTGTA[A/T]TATGTGAAAGGCATA | 64326 |
rs562410182 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176206992 | ATCGTGACTCCCTCC[A/C]CTCCAGCCGGGCGCT | 64326 |
rs562414189 | snp | C/T | | | intron-variant, utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175971589 | CACAGACCTATTCTG[C/T]GTACTCCACCCGCCA | 64326 |
rs562440053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176190116 | ATCATTCAAACTACT[A/G]CAGGGTGAATATCCA | 64326 |
rs562463947 | in-del | -/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175947605 | GAACTCCCAACCTCA[-/G]GTGATCTGCCCACCT | 64326 |
rs562473526 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176064097 | CCATCTGTACCTGAC[A/G]GATCTTTCAAAACTA | 64326 |
rs562477269 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176161563 | TGACTGTACCACTGC[A/T]CTCCAGACTGGGTGG | 64326 |
rs562480948 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176112313 | ATCTACATTTTTTTT[A/T]AATTTTATTATTATT | 64326 |
rs562484596 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176039765 | ATAAACTCTTGCATA[A/T]ATGGTCAAATAATTT | 64326 |
rs562494121 | in-del | -/A | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:175973708 | TAATTTCTACAATGG[-/A]AAAAAGTAAGTCTAG | 64326 |
rs562503760 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176158097 | AAAACACAAAGGGGG[-/A]AAAAAAAAACCTCTA | 64326 |
rs562512345 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175982914 | TTGGTCCAAGGCTAC[A/T]AAGTTTCAGCTAATT | 64326 |
rs562517272 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175974858 | ACCAATATGGGTGGT[C/G]AAGGCTGCAATGAGC | 64326 |
rs562520453 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176180784 | AAGAACAGCCAGGAC[A/C]AATCAGAACCAGTCA | 64326 |
rs562529071 | in-del | -/GTTAT | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176048682 | ACTTCAAGTGAACTA[-/GTTAT]GTTATCACTAAATAC | 64326 |
rs562531592 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176097878 | CATCTCAAAAAAAAA[A/G]AAAAAAAAAGCTCTA | 64326 |
rs562543960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176154092 | TTTTGGTATCAAGAT[A/G]ATGCTGGCCTCACAG | 64326 |
rs562550519 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176071018 | CAAAGCACTTAAAAC[A/T]CTTTATTCTAGATAT | 64326 |
rs562560446 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176002515 | TCCCCTTCCCCCCCA[A/C]CCCACAACAGTCCCC | 64326 |
rs562575838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176085714 | CATAAATTCAGCACA[A/G]AAACCTAGAAACAGA | 64326 |
rs562581127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176168245 | TGTATCTTTAGTAGT[A/G]ACAGGATTTCACCAT | 64326 |
rs562590738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176028542 | CAAAAAAAAAAAATG[A/G]AATGAAATGAAATAA | 64326 |
rs562601627 | snp | C/T | 1.77432e-05 | 0.00297847 | intron-variant, nc-transcript-variant, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175968431 | ATCAGACTTAGCCAG[C/T]TGTCCTAAGCCAGAC | 64326 |
rs562607149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176103976 | GAAATATTCTCTAAA[A/G]CAATGAAAAAGAGAA | 64326 |
rs562612981 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176199047 | TGGTGGCCGGGTGTG[A/G]TGGCTCACACCTGTA | 64326 |
rs562635198 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175973347 | ACCTAAACTTCTATA[C/G]TTTGCATGTACTAAT | 64326 |
rs562654100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176097341 | TAATTAAAAGCAAAT[A/G]GATCCCTCTCAAAAT | 64326 |
rs562655690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176104625 | CACCTAATATATTGG[C/T]AAAAATTAAAAACTA | 64326 |
rs562657956 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176187093 | CAATAGCTTTTAAGA[A/C]ATGTATTCTGAATAA | 64326 |
rs562661941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175974106 | TTTTAAACAGTGAGA[C/T]AAACAAGTCTAGAAC | 64326 |
rs562679616 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175998708 | CAGAGATGATTTTAC[C/G]TTTCTGGTGTAAGTT | 64326 |
rs562681783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176187541 | GGCATGAGCCACTTA[C/T]TCCTGGCTGAAATAC | 64326 |
rs562687069 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176052763 | TAGTTTCCTATGCAT[A/G]AACACGCATACACGT | 64326 |
rs562698166 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176003978 | TTGATTCTTCCAACC[C/T]ATGAGCATGGAATGT | 64326 |
rs562709879 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176093076 | AAATCTTACTATAAT[A/T]TTTTTATAAAGTTCA | 64326 |
rs562736233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176185513 | ATTGGCTATATGATA[C/T]TATTCTGGCCAGTGA | 64326 |
rs562744467 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176138527 | ACCCTGCTCACTCTT[A/G]AAGACACTGTCTGTC | 64326 |
rs562756205 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176124929 | TCTTCACTAGCATTT[A/G]TTACTGCCAAACTTT | 64326 |
rs562782678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176099598 | TAACTTATGGCAATA[C/T]AGTTGTTTACATCAG | 64326 |
rs562785084 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176054642 | TAACCAACATTTATA[C/T]TTGTGCGGTAAGTCC | 64326 |
rs562786992 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176194529 | TATAATCCCAGCTAC[G/T]AGGGAGGCTGAGGCA | 64326 |
rs562827729 | in-del | -/AAAC | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175997557 | AAATTTACAAGAAAA[-/AAAC]AAACAACCCCATGAA | 64326 |
rs562832691 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176054891 | TCCATAACCTCTCCT[C/G]TCGTTCTCTTTAACT | 64326 |
rs562836083 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176008029 | CCTCGGAGCCAGGTG[C/T]GGGATATAATCTCGT | 64326 |
rs562848390 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176080765 | CTTAAGCAAATTGAA[C/T]TGGTAGTTAAAATTC | 64326 |
rs562856100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176090980 | TTGTCTATACAGCAA[A/G]AATATCTTAAAACCA | 64326 |
rs562856585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176007321 | AGAGTAATTTGATCG[C/T]CTGAAGCCTTCTTCT | 64326 |
rs562863163 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176161070 | CTCCACAATATAAAT[A/T]GGGTCAGTTCTTAGC | 64326 |
rs562868942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176124631 | GCTGATAGTACTCCA[C/T]TGAGTATGTGTACCA | 64326 |
rs562873697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176006933 | CTACTGGATAATATC[C/T]TGCAGAGTGTTTTCC | 64326 |
rs562875021 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175996542 | GCTGATAAGCAACTT[C/G]AGCAAAGTCTCAGGA | 64326 |
rs562886332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176048895 | AAAGAATTAAGGGCC[A/G]GGCGCGGTGGCTCAC | 64326 |
rs562890005 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176025546 | ATAGGAAAAAAAATT[C/G]ACCAGAAAAGTCCAG | 64326 |
rs562915469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176027880 | CTAATAAAAAGATAC[C/T]TGAAACTGGGTAATT | 64326 |
rs562935855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992746 | CAAAGCAGCTGGGAA[A/G]CTCGAACTGGATGGA | 64326 |
rs562941076 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176112361 | GTACATGTGCACAAC[A/G]TGCAGGTTTGTTACG | 64326 |
rs562941454 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176000109 | GCAGAAGCTTTTTAA[A/C]TTGATATGATCCCAT | 64326 |
rs562947325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176145381 | CAGTGCAACAGAAAT[A/G]CTCATACAATGCCTA | 64326 |
rs562963618 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175999907 | CATTTATATGTCTTC[C/T]TTTGAGAAATGTCTA | 64326 |
rs562967035 | in-del | -/TG | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176095440 | GTAATCCCAGCTCTT[-/TG]GGAGGCCAAGGCAGG | 64326 |
rs562979680 | snp | A/G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176090645 | TTAAGCCCAGGGACC[A/G/T]CAAGTAGGGAAACTG | 64326 |
rs562992216 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176048355 | AATTTAAAAAAAAAA[A/T]TTATTCAGTTAAGTG | 64326 |
rs563000794 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176188437 | GGTTAAGGGAAAAAC[A/G]TATCCATTTAGAACC | 64326 |
rs563010007 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176084021 | TGTGATGACCTTTAC[G/T]ATTCCATACCATATC | 64326 |
rs563032256 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176012734 | TAGATACACGAATAC[G/T]TACCATTGTGCTATA | 64326 |
rs563042253 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175953782 | AAAAAAAAAAAAACT[C/G]CTATATACATATATA | 64326 |
rs563051919 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176084060 | CAGTGACTTAAAGAT[G/T]ACTAATAATAGCCTA | 64326 |
rs563057607 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176173508 | AGCCAGGTATGGTGG[C/T]GCATGTCTGTAGCCC | 64326 |
rs563063010 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176189109 | TGCTAAAACCAAAAA[G/T]AAAAAGAAAACCTTA | 64326 |
rs563070565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176035845 | AATGCATTTGAAATA[C/T]TTATCAAGGTAGTTC | 64326 |
rs563123391 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175994963 | TTCAGCACCACACAA[A/C]ACCTATTCCAAAATT | 64326 |
rs563133683 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | RFWD2 | GRCh38.p7 | 1:176048213 | TTTTTTTTTTTTTTT[C/T]ACAGAGATGGGGTCT | 64326 |
rs563134989 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | RFWD2 | GRCh38.p7 | 1:176005410 | TTTTGAATGTGTTTG[C/G]TCTTGCTTTTCTAGT | 64326 |
rs563136156 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176179268 | GCACTCCAGCCTGGG[C/T]GACAAAGTGAGACTC | 64326 |
rs563150512 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176112330 | ATTTTATTATTATTA[C/T]ACTTTAAGTTTTAGG | 64326 |
rs563172056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175965117 | TCTGTCTTCAGGGTG[A/G]GCTGTTACTATTTGT | 64326 |
rs563173108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176041492 | TAGCTAGGACCACAG[A/G]CCTGCACCACCACAC | 64326 |
rs563178308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176182993 | GGTGGACATTTGTAT[C/T]TTATATTACATCTTC | 64326 |
rs563184945 | in-del | -/A | 0.156319 | 0.231784 | intron-variant | RFWD2 | GRCh38.p7 | 1:176139289 | AAAAACAAAAAAAAC[-/A]AAAAAAAAAAACAAA | 64326 |
rs563187111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176041869 | CTGTAATCCTAGCAC[C/T]TTGGGAGGTTGAGGC | 64326 |
rs563206689 | in-del | -/TAGAAGTGCAA | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176205237 | GCACTATCGACTGTG[-/TAGAAGTGCAA]ACACTTCTCAGCCCC | 64326 |
rs563208925 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175994685 | AAATCAATTCAACAA[C/G]AAGAGCTAACTATGC | 64326 |
rs563213055 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176019533 | CATCATCACTACTAC[C/T]ACCACCAAATCATAA | 64326 |
rs563226730 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176131748 | CAGAATGTCTGATTT[C/T]AAATCGTAATCTTAA | 64326 |
rs563228868 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175952812 | GTCCCAGCTACTCCG[A/G]AGGCTGAAGCGGGAG | 64326 |
rs563248482 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176088139 | GGGATAGCACTAGGA[A/G]AAACACCTAATGTAA | 64326 |
rs563271826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176121612 | CTACTTTGACAGTTG[C/T]AACTTGGACATATAA | 64326 |
rs563295291 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175947590 | GGTCAGGCTGGTCTC[A/C/G]AACTCCCAACCTCAG | 64326 |
rs563304888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176045203 | TAGGTCTGCTAAAGA[C/T]CAAGCACTTAGGATA | 64326 |
rs563305642 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176168937 | CCAAGAAACCAAATC[C/T]ATCTTGAGTTATTTG | 64326 |
rs563332802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175957216 | TAATGTACAATAATG[C/T]CTGGGTCTTCACGTT | 64326 |
rs563336130 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176115142 | TAAGTCAAAACTTAT[C/T]TCAATACAAAGAGTT | 64326 |
rs563389614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176072387 | AAGACAGGTAAGGCC[C/T]CTGCCTAGATGAATC | 64326 |
rs563390100 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176052217 | ACCTACAGCATTCAG[G/T]ACAGTAACACGCTAT | 64326 |
rs563390857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176044481 | TTAGAAGGCAGTTAA[C/T]GTAGGTAACTTCTAA | 64326 |
rs563391565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176169757 | TAGGCTGGCTGTGGC[A/G]ATTTCTTAAAAGAAC | 64326 |
rs563399329 | snp | C/T | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176176687 | AGCCAGGCATGATAG[C/T]ATATGCAGCTACTGG | 64326 |
rs563420725 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175964143 | GGCACAGAAAGGTTA[A/C]ATAACTTTCCCAAAG | 64326 |
rs563423595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176135474 | AATGTTAAGATAAAT[A/G]TGACAGTAAGATAAC | 64326 |
rs563430933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176005096 | GAGGGTGTATGTGTC[A/G]AGGAATTTATCCTTT | 64326 |
rs563438748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176043462 | CATTTACCAAAATTA[C/T]TGCTTTTAGAAATTT | 64326 |
rs563443087 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176174977 | ACTAGTTATTATTTC[C/T]GATCATTTATCATTT | 64326 |
rs563450890 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176037125 | ACAAAAGAATAGGCC[A/G]GGCGCAGTGGCTCAA | 64326 |
rs563452994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175955844 | ATGCTTAGAGATGTT[A/G]AAGAATACCTAAATA | 64326 |
rs563455562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176073727 | GTCAAAGTAAACAAA[C/T]GCTGCCACCTTGTGG | 64326 |
rs563456971 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175946705 | ACACTAAAATAACTT[C/T]TTCTCCCCTTTGACA | 64326 |
rs563464461 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176128743 | TAAATAAGCATTAGT[A/T]CAATTTGATTATAAA | 64326 |
rs563469716 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176024568 | AACGCTCTTCACGTA[C/T]GATAAAAAGTTTTTC | 64326 |
rs563484194 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176205329 | CAATGAAAAACAGAT[C/T]AATTCTGATAAAGAA | 64326 |
rs563498287 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176164817 | TCTACAACCAACAAA[G/T]ATAAACTGACACAAA | 64326 |
rs563533631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176195544 | AGTGCATATGGACCA[C/T]TAGCGAAGATAAAGC | 64326 |
rs563535459 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207886 | AGTCAGTGAAGTTTT[C/T]TGCGAATTGCAAACA | 64326 |
rs563541164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175984871 | GTTTTGTTTTGGCCA[A/G]TTTCTCCCATTTTGA | 64326 |
rs563547195 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176174479 | TTTAGCCACTTAGAA[C/G]AATTTGTCATTCTAG | 64326 |
rs563557343 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176142805 | AAATATAATGAAAAT[C/T]AGAAATTATTTTGAA | 64326 |
rs563568939 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176038676 | TACAAAAATCAGCCA[A/C]GTGTGGTGGCGTGCG | 64326 |
rs563583536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176039163 | ATTAAACTAGAAATC[A/G]GTAACAGAAAAATAG | 64326 |
rs563586853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175977473 | GTTCAGCAGTAATAA[C/T]CTTTTTATTTTCCTG | 64326 |
rs563587268 | snp | C/T | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:175949404 | GATGTCCTTTAGGAA[C/T]ATAATAACTTACCCT | 64326 |
rs563591905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176127729 | ATGGGACTTTTTTCA[C/T]AGTGATTTTATTTCC | 64326 |
rs563608578 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176031608 | ATTTACATATGGCCT[C/G]CTTTGGCTCTCAGTA | 64326 |
rs563618184 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176072844 | AGGTGCAGAATTATA[C/T]GTCAAAAATTAGTAT | 64326 |
rs563625098 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176080382 | CAGATAAGAGCAAAT[G/T]AAACCCTCAAAAAGT | 64326 |
rs563626840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176036816 | GTAGGTTAGGCTAAG[C/T]TACGATTAGAAGTAT | 64326 |
rs563629545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175963233 | TTAATGCCTACAGAA[A/G]AAGGTCTAAACTTTT | 64326 |
rs563653994 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | RFWD2 | GRCh38.p7 | 1:175993895 | GGAAATATAGAGAAC[A/G]CCACAAAGATACTCC | 64326 |
rs563659753 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176078597 | GCAAATAATTTATGG[C/G]TAAGTCTTCAAAAGC | 64326 |
rs563663433 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175962890 | AGTTGTGTACTAGAA[A/G]GTAGAAGTTAATGAT | 64326 |
rs563671038 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176030184 | TGATTTGTTCCATGT[G/T]ATTCTCCAATAAGCA | 64326 |
rs563690557 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176120058 | GGAAAATCCTGGATT[A/C]GCCTCCACTTTGTAG | 64326 |
rs563721692 | in-del | -/TAAA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176046946 | TATCACAAAAGAGGT[-/TAAA]TAAATAAATAAATAA | 64326 |
rs563722913 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176202971 | AACACAAAATAGGCA[C/G]TCACATATTTACTGA | 64326 |
rs563757365 | in-del | -/CTA | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176093064 | ACAAATCTCAGAAAT[-/CTA]CTTACTATAATATTT | 64326 |
rs563762849 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176148394 | GCCAGTTAGAAATTT[-/A]AAAAAAAAAAAAAAG | 64326 |
rs563769644 | in-del | -/CTC | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175958551 | TTCCACCCTACATTT[-/CTC]CTCCTTTTATTAACC | 64326 |
rs563782932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176069219 | AGAAGAAAAGAAATT[A/G]TATGTAATACAGTAA | 64326 |
rs563798759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175990488 | AAGTGGTCTTTGGAT[A/G]TCTGTTATGTCAGAT | 64326 |
rs563814537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176030880 | AACAAAGTTAAAATT[A/G]CGTCAGACTAGATTA | 64326 |
rs563815935 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176013125 | TACAACATAAATGTT[G/T]TATGTAAATAATTGT | 64326 |
rs563819228 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176057579 | TAACCGCGAGTGATC[C/T]GCCAGCCTCGGCCTC | 64326 |
rs563832289 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175977623 | TAGGAGAGTGTCATG[A/C]GAACAACAGTGGTTA | 64326 |
rs563846238 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176034437 | CATCTGTGATATAAC[A/G]AATATGAAAAAGGCG | 64326 |
rs563870929 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176069746 | TCTTGTTTCCTTATA[C/T]TACCCAGAAGGCAGC | 64326 |
rs563875419 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176023850 | TTCTATCAAATATTT[A/C]AAGAAAATAATGCCA | 64326 |
rs563883367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176075866 | AAATTAGCCAGGCAT[A/G]GTGGTGGGCACCTGT | 64326 |
rs563883896 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176107848 | TATTCCTGACGAAAA[C/T]AGATAATCTGAATCT | 64326 |
rs563892508 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176008873 | TTAAGTCCAGCTGAG[G/T]AGGAGTTGTTCCTGG | 64326 |
rs563897848 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176026701 | AGTATAGTGACATGG[A/T]TTAAATTATGCATTT | 64326 |
rs563907977 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176062518 | ATTTAGAACTGGAAT[G/T]TTTTAAACTGCTGAT | 64326 |
rs563910955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176148838 | TTTTTAAGTGTCAAG[C/T]TGTAAAGAGAAAAGA | 64326 |
rs563912424 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | RFWD2 | GRCh38.p7 | 1:176058072 | GGCAGCCGCCCCGGC[C/T]GGGAGGGAGGTGGGG | 64326 |
rs563918717 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176067452 | TGCAGAGGAACACAT[C/T]GGTACAAGAGCACAC | 64326 |
rs563923215 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176120582 | TAACAGTGAGAAGCT[C/T]TGCTAAAAAAAGTAA | 64326 |
rs563957234 | in-del | -/CTCT | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176028786 | GACAGGTTCTCCTCA[-/CTCT]GTCATTCAGGCTGGA | 64326 |
rs563965751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175974179 | GGAGCTTGAACTAAA[A/G]GCAGGTGGTAGAGTC | 64326 |
rs563968652 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175986880 | TAAAATTTAATCAAA[A/C]CCTGTGTATACATAA | 64326 |
rs563975867 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176093039 | GGCATCAGCAATTAA[C/T]CTCTGAAAAAACAAA | 64326 |
rs564001311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175951218 | CATGCCACTGCACTA[C/T]AGCCTGGCCAACAAG | 64326 |
rs564010928 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176113471 | AGATAATCTGCCAAC[A/C]TTTTCTCACATTCTG | 64326 |
rs564014546 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176086342 | GACATTCTCCTGCCT[C/T]AGCCTCCCAAGTAGC | 64326 |
rs564016446 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176078032 | TCCTTCCATAAGCAT[A/G]ATTTGGAAGAATCGA | 64326 |
rs564020473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176163314 | TGCATGTAGTAAGGT[A/G]TTAAGCTCATTTGCC | 64326 |
rs564021105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176016065 | TGGGTTTGCAAAAGA[A/G]AAATTGAGTTCTGGA | 64326 |
rs564022640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176070093 | CCACGAACCCTGTTG[C/T]TACTTGAACAAGCTC | 64326 |
rs564022898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176061749 | AAGTTATTACAATGA[C/T]AGAAGAAAATATAGA | 64326 |
rs564038699 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176202364 | AGGCTAATTTTTGTA[G/T]TTTTTGTAGAGATGG | 64326 |
rs564049704 | in-del | -/A | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176173310 | GCGAGACTTTGTCTC[-/A]AAAAAAACAAAATGA | 64326 |
rs564050114 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992462 | GCCTCACTCGGGAAG[C/T]GCAAGGGGTCAGGGA | 64326 |
rs564051459 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176058582 | ATTAAGAGTCATCAC[C/G]ACTCCCTAATCTCAA | 64326 |
rs564057559 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175951871 | AGGAAGAGAAAAAAA[-/T]ATATGAAAACGTTAA | 64326 |
rs564059064 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176038740 | GGAGAATCGCTTGAA[C/T]CCGGGAGGCGGAGGT | 64326 |
rs564073311 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176172829 | GCCAACAGGAGACAG[A/T]CTCTACACACCTAGT | 64326 |
rs564088526 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176116335 | ACAGCATTCCAGCCT[A/G]CGTGACAGAGTGTCT | 64326 |
rs564102073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176187831 | AATATACATTAGTAA[C/T]AGGACTGGTGCTATG | 64326 |
rs564106250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176104673 | ATTCTGTTAGAGGTG[C/T]TGTGGGGAAAACAGA | 64326 |
rs564128994 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176140137 | CTCTAATGTCTTCTC[C/T]GAAAATAATGTTCCA | 64326 |
rs564129839 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176164849 | ACTGATTTTTTTTTT[-/A]AAAAAGGGAAACTAC | 64326 |
rs564157262 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175959546 | ATTAATTGTGTGCAT[-/A]AAAAAATCCAAGGAA | 64326 |
rs564181836 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175980861 | ATAATAGGGTATCTG[A/C]AGCCTCAAAAGAAGT | 64326 |
rs564206410 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176114777 | GTTTTTTGTAGAGGC[A/G]GGGTCTCACCATGTT | 64326 |
rs564209878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176019799 | CTGGAAGGCAGAGGC[C/T]GCAGTGAGCCAAGAC | 64326 |
rs564232639 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176062022 | TATTGTTTTTGGAGA[C/T]GGCATCTCACTCTAT | 64326 |
rs564233385 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176012940 | CACGTGATTGCATTA[C/T]GTAGTCCCTAGGTAT | 64326 |
rs564264773 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176122366 | GCATATGTACTCTGT[A/T]ACCTTTCCAAAATCG | 64326 |
rs564266505 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176142350 | TAAAACAAAAAATAA[A/T]ATGACAGGCTTATGC | 64326 |
rs564282793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176115614 | ATTAGCTGGGCGTGG[C/T]GGCGCGTGCCTGTAG | 64326 |
rs564288114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175984276 | TCCTGTGTCCCTGCC[A/G]CTCCAGCCATGACTA | 64326 |
rs564289295 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176018230 | ATTGTGATATTCTCC[A/T]AGAGTCAAAGAAGTA | 64326 |
rs564295883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176199644 | GTGTATTTCAAAACA[C/T]TATACCAAACGAAAG | 64326 |
rs564302232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176109351 | AATTTCCTTCAAATA[A/G]TTTCCCATTTGTCCC | 64326 |
rs564312469 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176169080 | TCAAAAGGAAGGCAA[A/C]GAAATGAGTCATGTT | 64326 |
rs564318046 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176153409 | TGTACTGACAGAAAT[C/G]AATACTAGTGATTTC | 64326 |
rs564328921 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175955234 | GTGACAGGAGTGAGA[A/C]CCTGCCTCAAAACAA | 64326 |
rs564335164 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176151210 | TTCGGATAAGGAAGC[A/G]TGTAAGAAAAAGAAT | 64326 |
rs564342244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176137434 | CAATCAAAAGAAAAC[C/T]GCTTTCCAGAAACAC | 64326 |
rs564370156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176040177 | ATATCTATTGTAACA[C/T]GGTACTCTCACTAAT | 64326 |
rs564378877 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175985456 | TTTCAGAGATTGATA[G/T]GAAGTTCAGATGCAA | 64326 |
rs564389377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176087409 | ACACAAAGAAATTTA[C/T]GAGAAAAAATCAACC | 64326 |
rs564406895 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176025198 | AAAGTAGATATTCTA[A/C]ACAGCAGAACACTAA | 64326 |
rs564421796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176012106 | GGAGGACTGCTTGAG[C/T]CCAAGAGTTTGAAGC | 64326 |
rs564422652 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175981551 | GCTTAAACATAAGAC[C/T]GAAAACTGTAAAACT | 64326 |
rs564439427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175979318 | AAATAAATTTTATTA[C/T]AGACATCTTTTATAC | 64326 |
rs564442969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176060183 | CTACTTTAAAAAAAT[C/T]TACTTTCTTATTCCC | 64326 |
rs564444774 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176067895 | AGCCCACGCTCCCAC[A/G]ATCTGCCTGTCTGTC | 64326 |
rs564451520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176204353 | AATTATCATTATTTG[A/G]ACTTGGGCTTCGTTT | 64326 |
rs564463329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176197369 | CAGTAAGCAGTGTGA[C/T]GGTGCCACTGTACTC | 64326 |
rs564478892 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176060842 | CAGAAACCCATTTTG[C/T]GTTTCTTATAAAAAT | 64326 |
rs564479656 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176150677 | ACAGTTCATTTACAA[A/C]GGAATTATACAAACT | 64326 |
rs564489732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176102687 | TAACAAATTAGCCAC[A/G]AGATTAGAAATTAAG | 64326 |
rs564492328 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176054861 | CTAATACCATAACTT[A/T]ACAAAAAAAAGTTTT | 64326 |
rs564502898 | snp | A/T | 8.40061e-05 | 0.00648043 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176184727 | AATTGATTTTTTTTT[A/T]AAAGTAGAGTGATTA | 64326 |
rs564514179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176053590 | CACTTCACACAACCA[C/T]GACCACACCCTAAAC | 64326 |
rs564520443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176106872 | GAGTGGTTACATGAC[C/T]AGCTCACAATTAGAG | 64326 |
rs564528101 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176006103 | TTTACCATTATGTAA[C/T]GGCCTTCTTTGTCTG | 64326 |
rs564531986 | snp | C/T | 0.00907127 | 0.0667334 | intron-variant | RFWD2 | GRCh38.p7 | 1:175982334 | GTATACAGCTGACCC[C/T]TGGAAAACACAGGTT | 64326 |
rs564533624 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RFWD2 | GRCh38.p7 | 1:175979966 | CACGCTGTGTAATGC[C/T]AGGGGTAATTAAAAA | 64326 |
rs564561716 | snp | G/T | 0.0314385 | 0.121371 | intron-variant | RFWD2 | GRCh38.p7 | 1:176165397 | GTGTGTGTGTGTGTG[G/T]GTGTGTGTGTAGGAG | 64326 |
rs564562950 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176178497 | CTCTGTCTCAAAAAA[A/C]CAAAAAATCAGCAAG | 64326 |
rs564593233 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176157754 | TTTATAATTTCTGGC[A/T]TCTAATTAAGAAACA | 64326 |
rs564600003 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207713 | TTCTGAGGGGTAGGC[A/T]GGTGCTTCCGAATCG | 64326 |
rs564605831 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175955514 | AGTCAAGAAAAGGAA[A/G]AAGCATATGGATCTG | 64326 |
rs564608361 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176112380 | AGGTTTGTTACGTAT[A/C]TATACATGTGCCATG | 64326 |
rs564644215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176047012 | CTCTCTTGCTGATCA[C/T]TTTTATATAAGCTCC | 64326 |
rs564665679 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176093124 | TAATATAGGGGTGTG[C/T]ATATATGTGGTAAAA | 64326 |
rs564666873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176097100 | ACTTGGGATGGCTAA[A/G]GTCAGGTAATAGGGG | 64326 |
rs564672821 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:175995417 | GAACTGAAGGAAATA[C/G]AGACACAAAAAACCC | 64326 |
rs564683948 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176177853 | AACTACTTTCACATC[C/T]CACATTTGTTACTTT | 64326 |
rs564705493 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176089178 | CAGTGGCAGGACCCC[A/C]GCTACTTGGGAGGCT | 64326 |
rs564710874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176002060 | AGAGTTTCAATATGA[C/T]GAGTTTAGGTGTACA | 64326 |
rs564733348 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176047828 | GCCTGCAATCCCAGC[A/G]CTCTGAGAGACCGAG | 64326 |
rs564734434 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176081641 | AGAAGAGTACTGGAT[A/G]AGTATTTGTTAGTTT | 64326 |
rs564737660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176050674 | AATTAAGAATTGATG[C/T]TACTCAACTTTCTTC | 64326 |
rs564741638 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176004086 | CTTGTAAGTTGGATT[A/C]CTAGGTATTTTATTC | 64326 |
rs564761821 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176134080 | AATTCTCCTTAACTA[C/G]AACATCCCTGCACCC | 64326 |
rs564767750 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176037204 | TCAGGAGATGGAGAC[A/C/T]GTCCTGGCTAACACA | 64326 |
rs564772774 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175966125 | TTGACTTGGTAAAAA[A/T]ATATATAAATATGTC | 64326 |
rs564778890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176096560 | TTGGTCTGAGCCAGG[A/G]GGAAAGGAACCCATT | 64326 |
rs564811954 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176064299 | ACATAAATAAGGATA[C/T]ATATTTTTAATATTA | 64326 |
rs564825977 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176049813 | AGATGACCTCTTATA[-/T]TAACAGTATGATATT | 64326 |
rs564836791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176106442 | CAAGATCAGAAATTA[C/T]AGTTTATAAGTTTAT | 64326 |
rs564850007 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176143378 | TAACTTAAAACTTCC[C/T]GCAAACAATCACAGG | 64326 |
rs564863793 | snp | C/G | | | intron-variant, downstream-variant-500B, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175968254 | CTATTTTCAAAACTC[C/G]TAAGATACCTCAAAA | 64326 |
rs564870563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176154701 | TAGGCTTAATAGCTG[A/G]GTGACAAAATAATCT | 64326 |
rs564872285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176141894 | CGCCCCTATGCTCCA[C/T]GAATTTTTTTTTAAT | 64326 |
rs564872348 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176133256 | TAGGTACACACATAC[C/G]TATATACGTACGTAT | 64326 |
rs564893368 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176038431 | CAAAGGAAATAGAAG[A/T]GTTAAAAATCATTTT | 64326 |
rs564910577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176175118 | CTAGTTCAGATTCTC[C/T]TCACCCATTCACTCC | 64326 |
rs564925316 | in-del | -/C | 0.0225045 | 0.103662 | intron-variant | RFWD2 | GRCh38.p7 | 1:176002506 | CTATCCCTTCCCCTT[-/C]CCCCCCCACCCCACA | 64326 |
rs564932631 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176091089 | AAAAGGACATCAATA[A/C]TCTTAAAAAAGTTGA | 64326 |
rs564935888 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176146184 | CAGAAGGGAATCATT[C/G]AAATGCTGGTACAAA | 64326 |
rs564939800 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176171934 | TTTAAATCAATATTT[A/C]AGTAACAAATCACTA | 64326 |
rs564943997 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175980343 | CAAGAATCAGAAGAA[A/G]CTTAGGTAAGCAAAA | 64326 |
rs564959814 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176064224 | AACCCAATGTAAAGT[A/T]TGAAAACTTACAATT | 64326 |
rs564963354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176162585 | AGACAGATAACCAAC[A/G]AAACTATTTCCTATG | 64326 |
rs564966344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176078690 | TAGCAGAAGAAATTG[C/T]CAACAGAGTAAACAG | 64326 |
rs564984003 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | RFWD2 | GRCh38.p7 | 1:175962559 | GGGTTTTCTTTCTAC[A/G]AGATATCCCCCACTA | 64326 |
rs564985372 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175987920 | GATAGGGGAAAATGA[A/G]TATCAAGCTTAAGAA | 64326 |
rs564988955 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176192994 | AAAACCTAAACACTG[C/T]ATATTGCATATACCA | 64326 |
rs564989365 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176185645 | AAAATTCTGATGCAG[C/T]GTTCAGAGATACAAC | 64326 |
rs565009719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175975521 | TTCAAGCGATTCTCA[C/T]GTCTCAGCCATCTCA | 64326 |
rs565015753 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176173041 | AATTGGGCCAGGGGC[A/G]GTGGCTCACACCTGT | 64326 |
rs565018116 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176044123 | GATGTCTATCAGTGA[A/C]GGTGATACTATCCAG | 64326 |
rs565026569 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175967547 | TGGCTGCTGTAAGTT[A/G]TAGAAGTTAGGGGAG | 64326 |
rs565044872 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176090347 | ACCTCTTGAGACTAT[A/G]CCTCAGGCCAGGGTC | 64326 |
rs565052217 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176181798 | CAGTGAGCGGAGATC[A/G]AGCCACTGCACTCCA | 64326 |
rs565052909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176186229 | GAGAAAGGGGTATTT[C/T]AGTGTTTGAGGATCC | 64326 |
rs565067726 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175965468 | TGATTTCCTGACACG[C/G]AGAATCATTCTTTTA | 64326 |
rs565074351 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175993907 | AACGCCACAAAGATA[C/T]TCCTCGAGAAGAGCA | 64326 |
rs565088423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175999377 | GTCTTTCTATGCCAG[A/G]CTTATTTCACTTTAC | 64326 |
rs565098575 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175953222 | ACTTTAGAGAAACCA[C/T]TAAAAAATACAAGAA | 64326 |
rs565111056 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:176086706 | AATTTATAAATTCAA[C/T]GCCATCCCCATCAAG | 64326 |
rs565113579 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175988550 | AGCACGTTCATCTGT[C/G/T]GGCCAGGCGTGGTGG | 64326 |
rs565114963 | snp | A/T | 0.0364509 | 0.129988 | intron-variant | RFWD2 | GRCh38.p7 | 1:176179876 | CAAAAAAAAAAAAAA[A/T]GGGACATAGCTGGAA | 64326 |
rs565124839 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | RFWD2 | GRCh38.p7 | 1:175997117 | ACAACTATCTGATCT[C/T]TGACAAACCTGACAA | 64326 |
rs565127855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176175721 | TGAATTTTTTAATAA[A/G]ACTTAAAAATAATAA | 64326 |
rs565137470 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176098290 | ATTGCTAAGAGTTAC[A/C]ATTATAATATGTAAT | 64326 |
rs565141020 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176123849 | TCAAAAACATGTCAG[C/T]AACACAGACTTATCA | 64326 |
rs565152776 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176047209 | TTCTAGAGGTTTAGC[G/T]ATAAGAATTCTCACT | 64326 |
rs565156304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176100141 | ACGCCTGTAATCCTA[A/G]CACTTTGGGAGGCCG | 64326 |
rs565158473 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176095546 | AATAAGCTGGGCATG[A/G]TGGCATACACCTGCA | 64326 |
rs565179321 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175963345 | ACCATCCTACTTAGA[A/C]ACTTTATTAGAAGTT | 64326 |
rs565181789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176051151 | TGATAGGACAAAATA[C/T]TGATAGAGGAATTCA | 64326 |
rs565192101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176093377 | ATTTTTTAATAATAC[C/T]AAGATTGTAATTCTA | 64326 |
rs565193369 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176188221 | CAATACTTAGGAAGA[G/T]TACTATCCACCCAAG | 64326 |
rs565203420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175993192 | GAGGGTCCTGTCTGT[C/T]AGAAGGAAAACTAAC | 64326 |
rs565209174 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176197229 | CCAACCTAGGCAAGA[C/T]GGCAAGACCCTCATC | 64326 |
rs565220653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176004609 | CATCTATTGAGATAA[C/T]CATGTGGTTTTTGTC | 64326 |
rs565237187 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175960800 | AGGTAACAGTGTGAT[A/G]GGTAATTTTAGGTTT | 64326 |
rs565257835 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176085479 | TATTTAATGTTAAAT[A/G]GGAGGCAACTGAATG | 64326 |
rs565271864 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176002560 | CCCTTCCTGTGTCCA[A/T]GTGATCTCATTGTTC | 64326 |
rs565279564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176003183 | TCTGTTCATGTCCTT[C/T]GCCCACTTTTTGATG | 64326 |
rs565284318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176118451 | CTATAGTTAACAACA[A/G]TGTATTTATATTTCA | 64326 |
rs565290842 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176208699 | GTTATCCTTGGCTAC[A/G]AAGATCAATAACAAG | 64326 |
rs565290904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176071623 | CTAAATAAAATGGCT[A/G]GAATTTGGTTTTAAA | 64326 |
rs565298153 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176071043 | AGATATTGACTGACA[C/G]AGTTTGGATATTTGT | 64326 |
rs565309947 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176042045 | TGAACCTGGGAGGCA[A/G]AGGTTGCAGTGAGCG | 64326 |
rs565310249 | in-del | -/C | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176064830 | AGTTTCACCATGTTG[-/C]CCAGACTGGTCTCGA | 64326 |
rs565320912 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176192203 | GATCTCTTCCTGGAT[C/T]TTATTCCATTCACAC | 64326 |
rs565337436 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175990859 | AACCTATTTGTGTCT[C/G]TGAATCTAAAGTCTA | 64326 |
rs565347641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175984513 | TCTGCCACGGCAGTA[C/T]AGAAGGGAAATGTGG | 64326 |
rs565347982 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175991407 | TGGTACACACCCATA[C/G]AGGGGACTTATGATG | 64326 |
rs565358279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176113979 | GTTTGCACAGTGACC[C/T]TGTTTTTTAAACGTG | 64326 |
rs565374704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176056169 | GTGATCAGAAAATGT[C/T]AATTTTTATTTTCTG | 64326 |
rs565377617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176138716 | GTTTTCCACCATAAC[A/G]TAAAAACCACTCTGT | 64326 |
rs565425869 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175983325 | TCCCGAACTGTTCTC[A/G]TGACAGTGAATAAGT | 64326 |
rs565430908 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175993860 | CCCAATCTAGCAAGG[C/G]AGGCCAACTTTCAGA | 64326 |
rs565433600 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175992868 | CTTAAATGTCCCTGT[A/C]TGACAGCTTTGAAGA | 64326 |
rs565443916 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176029439 | ATCATATCATTTTTC[A/C]ACAATAAAAACAGTA | 64326 |
rs565445391 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175961331 | AGAGAGAATAACTTT[C/T]AATCATCACAGTCGT | 64326 |
rs565453555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175946528 | GTACTCTCAGAAACA[C/T]GTACTCCACCAAAAG | 64326 |
rs565462151 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176177990 | TGCAAATATCTACTG[A/G]AAAATGACCTGCACA | 64326 |
rs565485216 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175964197 | GATAGGAGGCAAACC[C/T]GGCAACTTGGCTCCA | 64326 |
rs565487637 | in-del | -/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175980684 | CCTAATGACCACTGC[-/T]TTTTTTTTTGCCTGA | 64326 |
rs565491015 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176004577 | GGGTTGTTGCATTTT[G/T]TTGAAGGCTTTTTCT | 64326 |
rs565503309 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176051910 | TTATTGCAAAAAAAT[C/T]ACAAAGTCAAAAAAA | 64326 |
rs565518806 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176194435 | ACAAAGTCAGGAGAT[C/G]AAGACCATCCTGGCC | 64326 |
rs565522734 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176071727 | TCTTCCTTATATTAA[C/T]CTTAAAATGTGGCTT | 64326 |
rs565522944 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176109042 | GCTTGAACCCGGGAG[A/G]TGGAGGTTGCAGTGA | 64326 |
rs565538126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176132396 | TCCTAAGGTAGTGCA[A/G]TCATGCATCACTCAA | 64326 |
rs565549277 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175953849 | ATAAATTGACTCATG[A/T]TTGGAACTTTTAACA | 64326 |
rs565580957 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176167907 | GACTTCATGTACATA[A/C]AGGATTGAAAACAGT | 64326 |
rs565601834 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176131224 | AAAAATTTTAAGCAG[G/T]AAAGAAACATCATAT | 64326 |
rs565613184 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175956662 | TGCAAAATATAGTCA[C/T]GCACTGCACAATGAC | 64326 |
rs565622804 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176073180 | ATACAAGGATTAAAT[G/T]AATTAGGGAATTGAT | 64326 |
rs565629538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175957291 | CACCAAGCTCCATTC[A/G]TGGTAATGCCCTAGG | 64326 |
rs565643498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175948814 | CATGTGGGCATGGGA[A/G]TTGTTGATCTTTTCC | 64326 |
rs565653791 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176138176 | AAATAATAACATATG[C/T]GAAGGTACAAAAGCC | 64326 |
rs565661320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176163961 | ATCATGTAATTCTTC[A/G]GTTTAGATAGATTCT | 64326 |
rs565674050 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175994448 | AAAAGACACAGACTG[A/G]CAAACTGGATAAAGA | 64326 |
rs565696912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176065443 | TTGTCAAATATTTAT[A/G]TTATAAAACACTTGT | 64326 |
rs565709747 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176066497 | CTAATTGTAAAAAGC[A/G]TAAAAAAGAATAAAT | 64326 |
rs565722663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176164467 | ACCTAAGGCAATCTA[A/G]TCATTCATGCCCTTG | 64326 |
rs565726745 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176188930 | TGTAATTGAAGTCAC[A/C]GATGACAGAGAAAGA | 64326 |
rs565737033 | in-del | -/G | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176064805 | ATTTTTGCATTTTTT[-/G]TAGAGATGGAGTTTC | 64326 |
rs565759872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175948001 | TATGGATGGACATTT[A/G]GTATTAGGAAAACAA | 64326 |
rs565763336 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175965573 | CTTATCTGGGTTTTT[G/T]TTTTGTTTTGTTTTT | 64326 |
rs565783596 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:175972146 | CAACAACAAATACAA[A/G]AGGTGGTTCTTGGTC | 64326 |
rs565786451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176170139 | TACTTCCTCCACATA[C/T]GCAGTTACTCCCTCT | 64326 |
rs565793499 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176031167 | AGAGAACAAATTTCT[G/T]TTGTCTTAAGCCAGC | 64326 |
rs565796191 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176114589 | AATTCTTTTTTTTGC[A/C/G]GGGGGAGGGAGTGGG | 64326 |
rs565817838 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176127914 | ACACTTGTTTCATCT[C/T]TCTGATAATGGCCAA | 64326 |
rs565824493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176024667 | TCATAAATTGTTCAA[C/T]TGCAGATATGATTCT | 64326 |
rs565840207 | snp | A/T | 6.77438e-05 | 0.00581956 | intron-variant | RFWD2 | GRCh38.p7 | 1:176162842 | GTTCATCATTTAAAA[A/T]TTTTTTTAAGTTTAG | 64326 |
rs565842676 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176059713 | GTCTCGAACTCCTGA[C/G]CTCGTGATCCACCTG | 64326 |
rs565842790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176017611 | CTCACTAAAACCTCC[A/G]CCTCCTGGGTTCAAG | 64326 |
rs565845560 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176102105 | ATACCCATCTGCACA[A/C]TGAGAGGATGGGGTG | 64326 |
rs565848086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176157800 | AGAAAAATATATCCT[A/G]CAATAAGGGAAAAAG | 64326 |
rs565859090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176064806 | TTTTTGCATTTTTTG[C/T]AGAGATGGAGTTTCA | 64326 |
rs565898827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176016073 | CAAAAGAAAAATTGA[A/G]TTCTGGATGTTAAGT | 64326 |
rs565910281 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176112742 | CTCTGCCTACTACCT[C/G]CATTCCACTCTCTGC | 64326 |
rs565911364 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176173509 | GCCAGGTATGGTGGC[A/G]CATGTCTGTAGCCCC | 64326 |
rs565930059 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176182130 | GCAGGGCCTTTTTTA[A/C]AAAATGCCACAATGG | 64326 |
rs565937162 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175977784 | TTTTTGCTTAGTTAA[A/T]TCTGCTTTCAGTATT | 64326 |
rs565961168 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176086923 | GAGATACAGACCAAT[C/G]GAACAGAACAGATGC | 64326 |
rs565963368 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175964218 | CTTGGCTCCAGCACT[A/C]TCAATCAGAACATTA | 64326 |
rs565965545 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176049977 | AACAAACTTTAAGTC[C/T]TACTACTGCTATACA | 64326 |
rs565999908 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176199426 | CTCAGCAATTCACTA[C/T]TAGATATTTTTACCC | 64326 |
rs566011058 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176196226 | AAAGAAAACATGAAA[A/C]TCCAAGTTAGCAGAA | 64326 |
rs566015830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176039078 | CACATTCTGGGGCCA[C/T]AAAACACATCTTAAC | 64326 |
rs566023166 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176155456 | TTTAAATTCACAGGA[A/C]AAAAAGGAAAATAAG | 64326 |
rs566026494 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176201093 | GTGCCAACATGACTA[A/T]CAGAGGAAATGCTCA | 64326 |
rs566042541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176008189 | GTGAGGCAATGCCTC[A/G]CCCTGCATCAGCTCG | 64326 |
rs566043637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175976014 | TTAGTAAAGGGAAAA[C/T]CAGTTGTCAGATCTC | 64326 |
rs566045354 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176148009 | CAACTTTCATGCACA[C/T]TGCCATTTATATTGC | 64326 |
rs566063888 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176181639 | CAAGGTCACGAGATC[C/G]AGACCATCCTGGCTA | 64326 |
rs566076703 | snp | A/T | 0.0414363 | 0.137845 | intron-variant | RFWD2 | GRCh38.p7 | 1:176194938 | TAAAAAAAAAAAAAA[A/T]CAACCAGATGTGGTG | 64326 |
rs566086510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176152422 | AATAATGTTATGACA[C/T]TGTAAATTAGAAGTA | 64326 |
rs566089406 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175995436 | CACAAAAAACCCTTC[-/A]AAAAAATTAATGAAT | 64326 |
rs566096324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176054611 | CTTGTCATTCCGAAC[A/G]ATGTGCTCCTAGATG | 64326 |
rs566110180 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176142093 | ACCAAATAAATAAAT[G/T]ATAGAGTAGTGAGGG | 64326 |
rs566114344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176052316 | TTTGCACAACAAAAA[C/T]TGCCTAATGACACAT | 64326 |
rs566125247 | in-del | -/TTTT | 0.0166325 | 0.0896639 | intron-variant | RFWD2 | GRCh38.p7 | 1:176166126 | GCCTGTATTTATTTA[-/TTTT]ATTTATTTATTTATT | 64326 |
rs566129709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175983207 | AATGAAAAAGACTCC[C/T]CTGATATGGTTTGGG | 64326 |
rs566132662 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176055079 | GTGATTTTTCTCCTA[C/G]CTTACTGACAACTCC | 64326 |
rs566142017 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176008047 | GATATAATCTCGTGG[C/T]GCGCCGTTTTTTAAG | 64326 |
rs566155783 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176000154 | TTTGGCTGCTTGTGG[A/G]ATATTACTAAAGAAA | 64326 |
rs566157715 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176009648 | TTGGTATGTTGAGTG[C/G]TGACTTATTTTCAGC | 64326 |
rs566158331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176022621 | CGGTCAGTTTTCTAG[C/T]TGTAAAGTTTTTCTT | 64326 |
rs566191674 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176110949 | ATGAGATCAAGGGAT[C/T]GAGACCATCCTGGCC | 64326 |
rs566192330 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176197785 | TCCTATAGGTTCTAC[C/G]AAAAAATTATTAGAA | 64326 |
rs566203251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176037284 | TGGTGGCGGGTGCCC[A/G]TAGTCCCAGCTACTC | 64326 |
rs566214837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176195666 | GACATAGAATGATAC[C/T]CAGAAAATTCTCATT | 64326 |
rs566217396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175999596 | GATAGCTCTTTCATA[C/T]AGAAGTTGCCTTTCT | 64326 |
rs566224420 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176106628 | ATTGACCCAGTGCAA[A/G]AGGACAGCTTCAATT | 64326 |
rs566225471 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176148959 | CAAAATGGGAACAGT[A/T]AACAATAGTAAATAA | 64326 |
rs566230217 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175988886 | CCATGAAATCACAGA[C/T]AAATGACCATGTCAG | 64326 |
rs566239794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176043935 | GTCTCTATCAGTTCA[C/T]AATCATTATTCTGCC | 64326 |
rs566245443 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176151770 | AGTTAGATGTCTTTC[A/C]AACTGGGAGAAAACA | 64326 |
rs566248109 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176133780 | AGAGGAAAAAGACAA[A/T]GGGAATGAATCATTA | 64326 |
rs566248652 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176101207 | TGGGTGGCACCCTAT[C/G]GTGGCTGGTGGGACT | 64326 |
rs566262520 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176095846 | CATTACTATTCATAA[-/T]TTTTTTTAAAAAAAC | 64326 |
rs566283225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176134341 | AAGCATAAAAATTCA[A/G]AACTCAAGATTCAGA | 64326 |
rs566287106 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175964305 | AAAAGCATAACCTTG[C/T]TAAATAAGGATCTAA | 64326 |
rs566293790 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175956504 | TAAAGGAAAAAAAAA[A/C]CCCTGATAAATTGGA | 64326 |
rs566316071 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176119838 | ATTTAAACTTCACAG[C/T]TCTAATGTAGATAAT | 64326 |
rs566317486 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176082698 | GTAATCCTAGCTACT[C/T]GGGAGGCTAGGCAGG | 64326 |
rs566327049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175973344 | GCTACCTAAACTTCT[A/G]TAGTTTGCATGTACT | 64326 |
rs566329676 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176179441 | GCTGTTAAGTCAGAG[A/G]GGAGTTTGTTAGGCT | 64326 |
rs566332828 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176122483 | GTTTACTTAAGGAAT[A/G]CAAGGTTAGTTCAAT | 64326 |
rs566334770 | in-del | -/AGAAAGAAAGAAAGAG | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176151241 | AAGAGAAATGTATTT[-/AGAAAGAAAGAAAGAG]AGAAAGAAAGAAAGA | 64326 |
rs566351916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176191856 | TTAACATTGCCTTAA[A/G]TCACAGGCTCTATGA | 64326 |
rs566352423 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176008625 | CTAAGAATTTTTCTT[A/G/T]TTTGTGTATACCTTT | 64326 |
rs566355650 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176083581 | TTGGTTTGTAAAAGT[C/G]TATTCAATGTCTCTT | 64326 |
rs566360613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176141643 | TCCCATACTATCACT[C/T]CACAAACACTCACAT | 64326 |
rs566361717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175961029 | TCCTCTCTCCTGGAG[C/T]TGGGACACTCTTCTC | 64326 |
rs566367068 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176093762 | GGAGAATGCTGTGAA[C/G]CTGGGAGGCGGAGCC | 64326 |
rs566382438 | in-del | -/A | 0.0142736 | 0.0832652 | intron-variant | RFWD2 | GRCh38.p7 | 1:175952753 | GTTGCTACTAAAAAT[-/A]AAAAAAAACATTAAC | 64326 |
rs566388738 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176145555 | CTGGATACACATATA[A/C]CATAGTAGTATTTTT | 64326 |
rs566400889 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176125899 | CTTCTTCAATTTCTT[C/T]CATCAGTGCTTTATA | 64326 |
rs566422234 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176079994 | GAGACCCTGTCTCTT[-/A]AAAAAAAAAAATCAG | 64326 |
rs566423356 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176061366 | GGCATGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 64326 |
rs566435903 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176019291 | AATGTGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 64326 |
rs566444437 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | RFWD2 | GRCh38.p7 | 1:176006708 | TTGTAGGGTTTCTGC[C/T]GAGAGATCCGCTGTT | 64326 |
rs566448098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176011377 | ATCTACAAATATGTA[C/T]GGTGTAGTAAGTAGA | 64326 |
rs566450450 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175960054 | TCTTCATCACCTAAG[A/G]GAGGTCTGTAGGCTT | 64326 |
rs566460941 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176104137 | GGGCACATAGCTAGT[C/T]ATTTGGATGGATGAA | 64326 |
rs566465901 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176178996 | TTTAGTTTTTTTTTT[A/T]AAAAAAAGACAAGGC | 64326 |
rs566492964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176198558 | GATAACTTCTTAGCT[A/G]GAACACAAAAATTAA | 64326 |
rs566498645 | snp | A/C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176134440 | ATACCTACTACTAAA[A/C/T]GAAACCAGGCTTTAT | 64326 |
rs566514268 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176028020 | GGGCAGGCAAGAGAG[C/G/T]GTGTGCAGGGGAACT | 64326 |
rs566524511 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176116559 | TTTAGTAAACTAATC[C/G/T]ATGATTTTATAACTC | 64326 |
rs566534578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176109853 | TTTTGGTCTTTCTAT[A/G]TTTACCATCTAGTGA | 64326 |
rs566536879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176136649 | ACATTAGGAAAATAA[C/T]TTCTATCAAACTTGG | 64326 |
rs566539584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176069264 | CATAATGAAGCAATA[A/G]AAGTAAATATGTTAG | 64326 |
rs566540535 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176072775 | TCCTTGTAACTATCA[C/T]AGAAACATAAAGTTT | 64326 |
rs566546824 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175965940 | CGGAGTGTTTCTTTA[A/C]TTTATCCTAGACATA | 64326 |
rs566556771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176205419 | CCGTAAGTCTAATCA[A/G]TAACTTTCCTAACAG | 64326 |
rs566576175 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RFWD2 | GRCh38.p7 | 1:176152412 | AAATCTTGTTAATAA[C/T]GTTATGACATTGTAA | 64326 |
rs566582126 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175952596 | GAAGGAATATTATAC[C/T]ACATGAAAACTCTGA | 64326 |
rs566591841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176102773 | CTAAGATCAGTGCTT[A/G]AGATATTTTGCAGAC | 64326 |
rs566606022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176005711 | ATTGCACTGTGGTAT[A/G]AGAGATAGTTTGTTA | 64326 |
rs566616128 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176056247 | TTCCATGGACAATTT[A/G]AAAGAAGGTATATTC | 64326 |
rs566618578 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176110551 | ATATCTTACCAACTA[G/T]ATTGGAAACTTCATT | 64326 |
rs566623763 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176203194 | TACAAAAAATTAGCC[A/G]GGCGGGGTGGCCGGC | 64326 |
rs566627734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176139065 | AGAATCTACAAGGAA[C/T]GTAAATAAATGAAAA | 64326 |
rs566628326 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176059156 | CTGCTTCCATCCTAA[C/T]TGAGCAACCAGACTT | 64326 |
rs566638662 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176130899 | ACAAAACAAAACAAG[C/T]GGTTAATTCTATCTC | 64326 |
rs566649692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176090380 | TCATTTTGGTTTTTT[C/T]GGCTCCAAATAAACC | 64326 |
rs566655348 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176206224 | CAATTCATCAGAGAG[A/G]CAAAAATTTTAAGAC | 64326 |
rs566663308 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176006249 | ATGTGTGTCTCTGCA[C/T]GTGAGATGGGTTTCC | 64326 |
rs566670733 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175969223 | TATAAAGCAGATACT[C/T]TTAGGTAGAATCTGT | 64326 |
rs566680190 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175997269 | TGGATTAAAGACTTA[A/C]ATGTTAGACCTAAAA | 64326 |
rs566706006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176001325 | TGAGTACGATGTTAA[C/T]ATCATGCATAAGAAT | 64326 |
rs566739734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176145908 | AAGGGTGGTCAGGGT[A/G]CTTCAGCCGTTCTAG | 64326 |
rs566744989 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176088125 | GGGGGGATGGGTGAG[C/G]GATAGCACTAGGAGA | 64326 |
rs566750779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176007051 | CTTTGCTCATTTCTT[C/T]TTATTCTTTTTTCTC | 64326 |
rs566760223 | in-del | -/TGAG | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992091 | ATTTTTAATTTTTTT[-/TGAG]TATTATAGTTGGTAT | 64326 |
rs566768703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176158959 | GGTTCTTGTAATACA[A/G]ATGAAGTAGTATAAT | 64326 |
rs566797131 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175944962 | GATGGTGGAGAGTTG[A/G]CTGGGTATTCCCAAT | 64326 |
rs566799884 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176014413 | AGTTGCAACCTTTAT[C/G]TCTATTAAATGGAAG | 64326 |
rs566810557 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175994181 | ATAAAATACTTTACA[A/G]ACAAACAAATGCTGA | 64326 |
rs566815849 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176045054 | ATGTTTAAGGGCACA[A/C/G]ACTCTAGAACCAAAC | 64326 |
rs566818926 | in-del | -/A | 0.0410537 | 0.137264 | intron-variant | RFWD2 | GRCh38.p7 | 1:176190886 | GTACTGGTTCCAACT[-/A]AAAAAAAAAATCAAT | 64326 |
rs566838170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176033187 | GAGGCCGAGGTGGGT[A/G]GATCACTTAAGATCA | 64326 |
rs566839764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176025536 | GGTAACATATATAGG[A/G]AAAAAAATTGACCAG | 64326 |
rs566888583 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176088842 | CTGTACTAAAACTAC[A/T]AAATTAGCCAGGCAT | 64326 |
rs566898629 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176125385 | TGAGGCCTTTAAGTC[-/T]TTTAATCCACTTTGA | 64326 |
rs566910627 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175972549 | GGCTCACTGCAACTG[A/C]CACCTCCCGGGTTCA | 64326 |
rs566925139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176125791 | TTTGATAGTGATTGC[A/G]ATGTATCTGTAGATT | 64326 |
rs566927328 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176133458 | TCACTGACTGAAACG[A/T]CATTATGCAGTGCAT | 64326 |
rs566929879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175965401 | ACTATTCAATTGTCC[A/G]ATTTCATCACTCGTG | 64326 |
rs566933077 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176010170 | CACCGCCTCTTGTCT[C/G]TCTCTCTCTCTGCCC | 64326 |
rs566943048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176103400 | TAAAGCTCCTAAACA[A/G]TAAGATTGAATGAGT | 64326 |
rs566973952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176115940 | CTTTATTCCATGGAA[A/G]AGCTGTTAAGTTTCA | 64326 |
rs566987406 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175965803 | TGGTCAGGCTGGTCT[C/T]GAACTCCTGACCTCG | 64326 |
rs566991138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175958301 | TTATTCATGATTTAA[A/G]TATTTTCTGATTTCC | 64326 |
rs567016175 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176078530 | CTAAGACCTCAAACT[A/G]TAAAAATCCTAGAAG | 64326 |
rs567051947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992319 | TCCCAGAGTGAGCGA[C/T]GCAGAAGACGGGTGA | 64326 |
rs567065847 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175997964 | CATTATGTTTATTGC[A/G]GCACTACTTACAATA | 64326 |
rs567065911 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176004322 | TTTGACTTCCTCTTT[A/T]CCTAATTGAATACCC | 64326 |
rs567069080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175985890 | TAAAGTGAAACTATA[C/T]CTGAAACTTGGATTT | 64326 |
rs567071382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176171804 | CAGAATTTCAAGCAC[A/G]GAAATAGATTATAAG | 64326 |
rs567082502 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176094459 | TGCAGATAGTCTACA[A/C]GGCCAATCTTCAAAT | 64326 |
rs567092194 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176148351 | TATCCTAATTAGACA[A/G]TTCTTAACATAAACA | 64326 |
rs567095630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176023438 | AGAAAAAGTAAACAG[A/G]CCAGGCGTGGTGGCT | 64326 |
rs567104489 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176040276 | CTCACCTCCCTTCCT[C/G]TCTCTCTCCTTCTCC | 64326 |
rs567110898 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:176171374 | CACCTCTCTGAGCCT[C/T]CACAGAATTTAGGAG | 64326 |
rs567120945 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176079181 | TTCCATAAAGACACA[C/T]GCACTGGTATGTTCA | 64326 |
rs567127730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176178018 | ACAATGTTCCAAAAA[C/T]AGTATCATCACCTCT | 64326 |
rs567134220 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176147139 | TGTATTTTACTTGAA[C/T]AAGTTCAAGTATATA | 64326 |
rs567151326 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176155556 | AAAGGAAGGAGAGCA[A/T]AGGGCTGAACAAGTA | 64326 |
rs567151756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176122736 | AAAATGTTTATTACA[C/T]AATAATTCTGAAACT | 64326 |
rs567176641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176086398 | GCCCAGCTAATTATA[C/T]TGAATTTTTAGTAGA | 64326 |
rs567180437 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176106187 | GGCATACATCACCAC[-/A]ACCCTGCTAATTTTT | 64326 |
rs567185896 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176073561 | AATGCAAAATATGCT[A/G]TTATTGCTGTGTGTA | 64326 |
rs567188669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175995460 | AATGAATCCAGGAGC[C/T]GGTTTTTTGAAAGGA | 64326 |
rs567213535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176091389 | CTGAAGTTGTGTACT[C/T]GAATAATACAATGAC | 64326 |
rs567227995 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176008077 | GCCGGTCGGAAAAGC[A/G]CAGTATTTGGGTGGG | 64326 |
rs567232667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176030417 | GTGCCCATAACCCCA[C/T]TTATAATCACTAAAA | 64326 |
rs567243665 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176086001 | ATCACAGTAAAATGA[C/T]CACAAATAGTAAAAA | 64326 |
rs567267849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176174548 | ATGTAATCCTCCAGC[A/G]ATTTTCCTTCATAAA | 64326 |
rs567269684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176181568 | ACATTCTTGGCTGGG[C/T]GCAGTGGCTCACGCT | 64326 |
rs567274199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175993639 | AACTGGAAGAAAGGG[C/T]ATCAGTGATGGAAGA | 64326 |
rs567279251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176077405 | AAAACAAAAAACATA[C/T]GATCATCTCAACAGA | 64326 |
rs567288720 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176036928 | CCCATAAATCTTGTA[A/G]CAAATAAAATGTATC | 64326 |
rs567291105 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175963903 | TCACTTAAATGCAGA[G/T]AATATATTTTCATAT | 64326 |
rs567292255 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175988669 | AAAACACCGTCTCTA[A/C]TAAAAATACAAAAAT | 64326 |
rs567304282 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175955090 | CTCTCTATCAAAAAC[A/G]CAAAAAATTAGATGG | 64326 |
rs567316448 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175988101 | TCTACACAATAAAAA[A/T]GGGAAGGACTAATGC | 64326 |
rs567325773 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176187115 | TCTGAATAACAAGAG[A/C]ATCAAAGAAGGTCTC | 64326 |
rs567328429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175962054 | AAGATTAATTTATCT[A/G]TGAATTTTATTTATG | 64326 |
rs567333237 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175988603 | TTTGGTAGGCCGAGG[A/C]AGGTGGACCACCTGA | 64326 |
rs567335959 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176140968 | AGGTAAAGAGTAAGT[A/C]AGTCTCAGAATCCCT | 64326 |
rs567341355 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-5-prime, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207165 | GTCCCACGGGAGGGG[A/G]CGGAGGAAACTAAAA | 64326 |
rs567359159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176050764 | GTTTTAACCACCTTA[C/T]ATAAATTATACAAGC | 64326 |
rs567391646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175954370 | CCTTAAGAAGCTAGG[A/G]AAAGAGCAAGTTACA | 64326 |
rs567404329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176180925 | TGGGAGATGACGATG[C/T]TGAAGGACCCCATTA | 64326 |
rs567415042 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175953266 | AATAAGCTAGTAAAG[C/G]AGAAAAAATATTATA | 64326 |
rs567421375 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176042537 | CACTGCACTCCAGCC[C/T]GGGCAGCAGAGCGAG | 64326 |
rs567422484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176186044 | ATATACAATAATGAT[A/G]AATACATAATAATAA | 64326 |
rs567424331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176072499 | CTGCACTCCCATTCA[C/T]CTCATTTCTCAACCA | 64326 |
rs567448157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176037249 | CTACTAAAAATACAA[A/G]AACAAAAATTAGCCA | 64326 |
rs567452582 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176068594 | ATATGATTAATTGAG[C/G]CTATTTCCAGTTAAG | 64326 |
rs567462914 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176140927 | TGCCAAAGCCCAAAG[A/G]AAACTTTTAGAAACA | 64326 |
rs567465827 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175983294 | GGGAGGTAAATGACT[C/G]ATGGGGGCAAGTCTT | 64326 |
rs567466574 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176113185 | ATAGGGGCATTCACT[C/T]TTTCTCCACGTCCTT | 64326 |
rs567476075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175983683 | AAAATGTGGGAAAAT[C/T]TGGAACTCCCTAGAG | 64326 |
rs567481537 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175994023 | ACCACAAAGGGAAGC[C/T]CATCAGACTAAGAGG | 64326 |
rs567495982 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176099069 | TGTTATGTTAAGTTA[C/T]TGTAAACCACAGAGA | 64326 |
rs567497016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176065575 | ATTCTTTTGAGCTGA[A/G]GACAATGGAAAAAGA | 64326 |
rs567502783 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176154330 | TGCATTATAAAGACA[C/T]ATGCACATGTATGTT | 64326 |
rs567507564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176106557 | CACTTGACAGATCAG[C/T]TGGCAACACCCAGAT | 64326 |
rs567510709 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176073010 | AAATCCTTAAGTGAA[A/T]AGAAGAGCACTAGAA | 64326 |
rs567529346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176175205 | AAACCTGAGTTCCCG[A/G]GACCCATGGACTCTT | 64326 |
rs567532200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175947029 | TCATCTTCTCCACAG[A/G]TGCAAGCTACCTATT | 64326 |
rs567561378 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175956131 | AGGAATCAATACAGT[C/G]TAGTATTATTAGGAT | 64326 |
rs567564327 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:176111440 | CTGGGACTACAGGTG[C/T]GCACCACCATGCTCA | 64326 |
rs567573419 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176169293 | ACTATAGAATTTTAT[A/G]TCTAAGACTTCATAA | 64326 |
rs567579572 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176078828 | AAAATCCAATAAAAA[A/T]TGAGAAGACACAGAC | 64326 |
rs567584770 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176103164 | ACACACAGTTCCTAA[A/G]ATCCTTGGAGTTTCC | 64326 |
rs567594589 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:175982435 | CTTCTTTCTCCTCCT[C/T]CTCAGCCTACTCCAT | 64326 |
rs567596132 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | RFWD2 | GRCh38.p7 | 1:176063173 | CACGCCATTCTCCTG[C/T]CTCAGCCTCCCGAGT | 64326 |
rs567601875 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176072517 | CATTTCTCAACCAAC[A/C]CCAGATGGTCAATAA | 64326 |
rs567602712 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176200036 | CTGACCTCTGAGCCA[A/T]ATTGTCTGAATATAA | 64326 |
rs567615751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176173272 | GTCAAGATCATGCCA[C/T]TGCACTCCAGCCTGG | 64326 |
rs567635326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176021024 | TGTTTCCCAGGATGG[A/G]CTGCAGTGGCACAAT | 64326 |
rs567647451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176099804 | GGTTCCTGACCTGTG[A/G]TAAGTAAAGAATGTC | 64326 |
rs567649788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176160214 | CAGTTCTCACTTTCA[C/T]TATGTAATTATCTGC | 64326 |
rs567663482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176200855 | ATGCTTACAGAATTT[C/T]GTCCTACATACAACA | 64326 |
rs567677035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176167176 | GTCATTAGAGTCACA[C/T]ACTTAGTGGGAAAAC | 64326 |
rs567707834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176147171 | ACCATATTACAGGTC[C/T]TAAGACCTGTAACAA | 64326 |
rs567708389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176203036 | TTCTATCAAGCAGAT[A/G]ATTAAAAGTCAACCT | 64326 |
rs567710069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176161226 | TGCCTCTTTAAAATC[C/T]CTAATTTACTGTCAT | 64326 |
rs567713101 | in-del | -/TATTAACCAAAAGTAAAGGGAAGGGGTCAGATTCC | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176015418 | GAAAGACAGACACTT[lengthTooLong]TATTAACCAAAAGTA | 64326 |
rs567714494 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175985064 | AGACTGCTGGGAAGG[C/G]ATGATCAGTTTTGAA | 64326 |
rs567721237 | in-del | -/A | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176077394 | AATAGAATAAAAAAC[-/A]AAAAAACATATGATC | 64326 |
rs567726934 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175985685 | AATCCAAATCTGGTA[A/G]TTCTTTCCTGTCTTG | 64326 |
rs567727929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176195887 | TGAGGATTCCAAAAT[C/T]GGGGACGGAGGGGGT | 64326 |
rs567748029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176035424 | CGAAAGGGTCTAATA[C/T]ACTAACATAATTAAA | 64326 |
rs567759700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176067623 | CCTCTCCATCAACCT[C/T]CCTAACAGCTACCAC | 64326 |
rs567765169 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176150604 | AGAGGACAAAGACCA[C/T]ATGTTTATTTAAAAA | 64326 |
rs567772291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176186661 | GAGGAGTGATGGGAT[C/T]TGACACAGTAATGAA | 64326 |
rs567781063 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992877 | CCCTGTCTGACAGCT[C/T]TGAAGAGAGCAGTGG | 64326 |
rs567806126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176140205 | CTATTGTTACATATG[A/G]AGGCTTCTATACATA | 64326 |
rs567811469 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175949701 | ATGCTGCAGCCATCA[G/T]GAACTGCTCCCTTTG | 64326 |
rs567814059 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176007945 | CCCCTCCCCCAGCCT[A/C]GCTGCCGCCTTGCAG | 64326 |
rs567837847 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176171157 | AAAAAAAGTAGGCTG[C/T]TATATCTACACTGAA | 64326 |
rs567838833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175974601 | GGAAAAGATATAAAA[C/T]GTTTAAGATCGAATA | 64326 |
rs567847141 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176013629 | ACAAATGTATTTCAA[A/C]TCACCATATAATATG | 64326 |
rs567851442 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176103205 | CAGCATCTTTTGTTA[C/T]TCACAGCAAGTTCCT | 64326 |
rs567856190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176203424 | AAGAATGGCTGGGAC[C/T]TGCAGAGGTAGAAAA | 64326 |
rs567879119 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176100998 | GCATAGGTTAGTGTG[A/G]CTGATTCTTACTAAG | 64326 |
rs567889588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176147680 | CATCCAGAAGTTTAA[C/T]AACGGAAATATAAAA | 64326 |
rs567892639 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176183708 | GAAGAAGCAACCCCA[C/G]TGTATACTGATAGAT | 64326 |
rs567898907 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176096285 | TTTTTTTTCAGGACA[A/G]TAACAGCACCTATCT | 64326 |
rs567909737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176193421 | TACACTGTGAGTAAA[C/T]GCCCCAGAGACTAGA | 64326 |
rs567919061 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176097687 | CAGCCTGGCCAGCAT[A/G]GTGAAACCCCATCTC | 64326 |
rs567925631 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176063750 | TTTGGGGGGCTCTGT[C/T]TGATAAATAATTGTA | 64326 |
rs567935424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176001426 | TTTGTTTGTGTAAAT[A/G]GAAATACCACTACTA | 64326 |
rs567952451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176014214 | CAAGTGGGAAGCTGC[A/G]CTTACATTTGAAAGG | 64326 |
rs567952750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176068513 | ACGACTAACATTTAC[A/G]TAGTATTTACAACAT | 64326 |
rs567962303 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175973198 | TTGGTTAAAAGATAC[C/T]ATAATCAGTACTGGA | 64326 |
rs567966507 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176120596 | TTTGCTAAAAAAAGT[A/G]ACAACAATGCAGCTG | 64326 |
rs567978237 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176115365 | TGAGGCTGGAGAATC[A/G]CTTGAACCCAGAAGG | 64326 |
rs567978873 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176127444 | GTAAGCAAGATCATA[C/T]AATATCTGTCTTTCT | 64326 |
rs568012739 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176157941 | GAACAACTTCAACTA[C/G]CCTAAGAGATATGTA | 64326 |
rs568036565 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176025381 | ACTAAAAAGCTACTA[C/G]ACTTAATGTAAAAAA | 64326 |
rs568040092 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176019263 | AGGTCAGGAGTTCGC[A/G]ATAAGCCTGACAAAT | 64326 |
rs568051863 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176157210 | AAAAAATAATAACAA[A/C]AACAATAATATTAAT | 64326 |
rs568063759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176108747 | TTCATGTGAGCTGAA[C/T]GTGTGAATTTTTGTC | 64326 |
rs568101748 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176049921 | ACTAAATAAAAGGTA[A/C]ACTAATTAACTGAAA | 64326 |
rs568118423 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176052451 | CTCCTACTCCTGAAA[G/T]TTCCCTCTTCCAATC | 64326 |
rs568135593 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176181468 | AGCCTGATGTTGGAA[A/T]TGACAGCCTCCAGTT | 64326 |
rs568147986 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175972630 | CGGCCATGCCCGGCT[A/C]ATTTTTGTATTTTTT | 64326 |
rs568152437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176191009 | TACACCTCACATAAA[C/T]AGGACTGCAGAAACA | 64326 |
rs568159503 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176032453 | TAAAGCTTAGCTACT[C/T]AAAACAGCAAACATA | 64326 |
rs568171880 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176164534 | TTTGACCAAAGAGAG[A/T]TGTGCTATCTTTCAG | 64326 |
rs568175562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176114605 | GGGGGAGGGAGTGGG[A/G]GGGAAAGGGTCTCAC | 64326 |
rs568201213 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176024024 | GCACTTTGGGAGGCC[A/G]AGGCAGGCAGATCAC | 64326 |
rs568211465 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:175965857 | AAAGTGTTGGGATTA[C/G]AAGCGTGAGCCACCG | 64326 |
rs568212668 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RFWD2 | GRCh38.p7 | 1:176151363 | AAAGAAAAAGAAAGA[A/G]AGAAAGAAAGAAAGA | 64326 |
rs568215789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176109090 | GCACTCCAGCCTGGC[A/G]ACAGAGTGAGACTCT | 64326 |
rs568231191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176156174 | AGTAAACTGAGTTAT[A/G]TGGTATACCATATAT | 64326 |
rs568231239 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | RFWD2 | GRCh38.p7 | 1:176148394 | GCCAGTTAGAAATTT[A/T]AAAAAAAAAAAAAAG | 64326 |
rs568238164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176183490 | AAAATTGGAACTCTT[A/G]TGCACTGTTGGTGAG | 64326 |
rs568244931 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176060338 | AGATGCCCTTTAAAA[A/T]CAATATACTTAATAT | 64326 |
rs568250348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176054456 | AATGACCCACTGCAC[C/T]CGGCCAAATTACTCT | 64326 |
rs568256588 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176023424 | ATATGAATTCACCTA[C/G]AAAAAGTAAACAGGC | 64326 |
rs568264859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176006606 | TTCTCCTTTGCTTAC[A/G]AAGCTTAGTTTGGCT | 64326 |
rs568274013 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175975031 | TTTTAAAAAATATTG[A/T]CAGCTGTCAGTAAGA | 64326 |
rs568275657 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175994499 | TGTATTCAGGAAACC[C/T]GTCTCACGTGCAGAG | 64326 |
rs568285266 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176136017 | AAATCATAATACCCT[A/G]TAAGACTCCCAAGGA | 64326 |
rs568306606 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176046604 | TCAGTTCTAATAACC[A/G]TATTACAGCTTACTG | 64326 |
rs568335281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176088859 | AATTAGCCAGGCATC[A/G]TGGTGCATGCCTGTA | 64326 |
rs568345707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176018548 | CTCCCTGTCTGCTTG[A/G]GCCATCTTTTCCTAC | 64326 |
rs568350824 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175948976 | GAGACCATCCTGGCT[A/G]ATATGGTGTAATCCT | 64326 |
rs568355387 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176158766 | TACCTCTGCCTCCCA[A/C]GTAGCTGGGACTATA | 64326 |
rs568367023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176182156 | AATGGATATGTAAGT[C/T]ACAGGACACTCAAGA | 64326 |
rs568373092 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176044731 | ACAGTAGATGTGCTC[C/T]GAATCTATTTTAGGC | 64326 |
rs568374046 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176190408 | CTGTTTATTAAAATC[G/T]TGTTCTTCAAGCAAT | 64326 |
rs568377444 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176150877 | TCTTCTGCAGTTTAA[A/T]CTTTTTAAAGGAAGA | 64326 |
rs568382034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176109506 | AGTACATTTTAATAG[C/T]TGATGAGGTAAATTC | 64326 |
rs568412108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175971571 | GTTTCCAAGAGTCAC[C/T]AGCACAGACCTATTC | 64326 |
rs568413428 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175995300 | ACAAAGCAGGAAAGA[G/T]CCAAAATTGACACCC | 64326 |
rs568428412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176176120 | TCAACATAACTAATC[C/T]AATAAATTTATTTTT | 64326 |
rs568429036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175970275 | GGAAAGAGAAGCAGT[A/G]ATTGGGCTAAAAAAT | 64326 |
rs568433316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176188689 | TTTGATGTTACTACC[A/G]TAACTGTTTTGGGGA | 64326 |
rs568438843 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175949465 | GGCCTCAGAAAACAG[C/T]AGAAAGAGGCACTGT | 64326 |
rs568441189 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RFWD2 | GRCh38.p7 | 1:176066285 | TTCAGCCCCCATGCC[C/T]CATGTCATGTAAAAC | 64326 |
rs568452253 | snp | G/T | 0.0402882 | 0.136092 | intron-variant | RFWD2 | GRCh38.p7 | 1:176101216 | CCCTATCGTGGCTGG[G/T]GGGACTCGGGATCCA | 64326 |
rs568465222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176146033 | TTTTCATATAAAAAT[C/T]GTTTAAAATTCAATT | 64326 |
rs568479866 | snp | A/G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176030459 | CAAGCATTATGTATC[A/G/T]TTGTTTAACGTTAAT | 64326 |
rs568480864 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176142255 | CATTATAGATAAATC[A/T]AAATGGAATTCCGAA | 64326 |
rs568506463 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176150154 | ATCACTAAGATATAA[C/T]ACGTACTACAAATAA | 64326 |
rs568512490 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176099763 | AAAAATGGCCTCATA[C/G]CCTTGTCTACACAGC | 64326 |
rs568518587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176049038 | TTAGCCAGGCGCGGT[A/G]GCGGGCGCCTGTAGT | 64326 |
rs568519367 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176057885 | CATCCCATCTAGGAA[A/G]TGAGGAGCGTCTCTG | 64326 |
rs568525559 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176016235 | GATAAAATAACCCAT[A/G]GGGAATTTAGAGAGT | 64326 |
rs568529545 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176081608 | AAAAATCCATCAATG[G/T]AGAATGTGAGGATAT | 64326 |
rs568530173 | in-del | -/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175992083 | TTTGAACATTTTTAA[-/T]TTTTTTTTGAGTATT | 64326 |
rs568530187 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176134938 | ACTGCATGGAAAAGG[A/C]TCCTAAAGGACTAGA | 64326 |
rs568536207 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175976996 | AACTATTAGTATTTT[G/T]TTCTCCCAATCTCTG | 64326 |
rs568542268 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175977028 | AAATCATTTCACAAA[G/T]ATATGTTTGGTGAGT | 64326 |
rs568549496 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176123781 | GTTTGTGTTGAATAT[C/T]TGAACTTTCTCTTAT | 64326 |
rs568549517 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176146873 | TAAGGAGAATCAGTA[C/G]GAAAAAATAAAACTG | 64326 |
rs568557380 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176130063 | ACATTTGTTAATCCA[C/T]ATAACGTCCACCCAG | 64326 |
rs568586662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176008660 | ACTGAAAAGCAGACA[C/T]TTTGGAAAATACTAT | 64326 |
rs568594935 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175999687 | TTAGGAATCTCCAAA[C/T]CAATCTTCATAGTGG | 64326 |
rs568597199 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176038750 | TTGAACCCGGGAGGC[A/G]GAGGTTGTGGTGAGC | 64326 |
rs568598005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176012583 | ATGACCTAGGTCTTC[A/G]TATTCACTCACCACT | 64326 |
rs568598248 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176195770 | TCCATTATCCTAAAC[G/T]GATTAACACAAAAAC | 64326 |
rs568631405 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176189333 | TTGTCATTTGTTTTG[G/T]TCATATTTTTCTGGC | 64326 |
rs568633659 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176206259 | CCTCTCTGCCAACTT[A/T]GTTATCCAAAACCAT | 64326 |
rs568639838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176143070 | AGTTAGTTATTAGAA[A/G]AAAACCCATATAATT | 64326 |
rs568667320 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175990526 | GTTATTCAAGTCTTC[A/T]AAAACTCTGCCAATT | 64326 |
rs568670089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176031338 | TAGAAGAAATCAAGT[A/G]TGAGAAGAAACTAAG | 64326 |
rs568670908 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176056117 | TATATTTTTCCTGTT[C/T]TCTAAGTTTGTAATA | 64326 |
rs568670959 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176128021 | CTATGTCTTCTTTTC[C/T]ATGTCTTCTTTTGAG | 64326 |
rs568679882 | snp | A/C | | | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176208995 | GAGGCAGGAGAATCG[A/C]TTGAACCCAGAAAGC | 64326 |
rs568680095 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176035426 | AAAGGGTCTAATACA[C/T]TAACATAATTAAAAT | 64326 |
rs568686400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176173806 | CAGCCTATCCAACAT[A/G]GTGAAACCCCGTCTC | 64326 |
rs568693106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176182592 | ATAGTGACAAGGTTG[A/G]GAAAGCCTACTCTAG | 64326 |
rs568700845 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176026807 | TTAATAAAAAATAAG[A/C]CTTCACCATTCAGAA | 64326 |
rs568712289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176029853 | CAAGTAGAAATTAAT[C/T]ATTATCAAAAAATAT | 64326 |
rs568713639 | in-del | -/T | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176016150 | TAGAAATGTCTGGAG[-/T]TTTTTTTAGCTAAGA | 64326 |
rs568753340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176185785 | GGACTTCACATTACA[C/T]GAGAAGGTAAATCTT | 64326 |
rs568770694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176095330 | TGAGGACCACTGGGA[A/G]TTCTCTAAGATCTTT | 64326 |
rs568801337 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176000263 | TTTAATCCATTGTGA[C/G]TTGATTTTCATATAT | 64326 |
rs568803549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176055552 | GTCTCATGACTTTCA[A/G]TCTATATAGTACACT | 64326 |
rs568841137 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176055177 | AGTGGCTCAAGCCTG[C/T]AATCCCATCACTTCG | 64326 |
rs568856897 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RFWD2 | GRCh38.p7 | 1:176002806 | ATTGTGAATAATGCC[A/G]CAATAAACATACGTG | 64326 |
rs568864054 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176193162 | ATGAATGGCCAACAA[C/G]CTCTTGAAAAGATGG | 64326 |
rs568873905 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RFWD2 | GRCh38.p7 | 1:175967291 | TGATGGGACTACTGG[A/C]GTGAGCCACCGCGCC | 64326 |
rs568883331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175967810 | ATCTAAAGTATTGAC[C/T]TTCACTGGTAACCCT | 64326 |
rs568904792 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175995545 | ATCAAATAGATGCAA[A/T]AAAAAATGATAAACG | 64326 |
rs568917347 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175996116 | ATCAATAAATGTAAT[A/C]CAGCATATAAACAGA | 64326 |
rs568944392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175981722 | AAGACAACATGTGGA[C/T]TGGGAGAAAATATTT | 64326 |
rs568984350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176096844 | AAACTTTGCTGCAGG[C/T]CTCCATCTTGTTTTA | 64326 |
rs568987964 | in-del | -/A | 0.11269 | 0.208916 | intron-variant | RFWD2 | GRCh38.p7 | 1:175961911 | TGGAATAAATTTGAA[-/A]AAAAAAAAATGGTTT | 64326 |
rs568997168 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176131997 | CAACAATATTTTCAT[A/G/T]AACTTCATGAAATCT | 64326 |
rs569033527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176084472 | CCATCAAGCTACCAA[C/T]GACTTTCTTCACACA | 64326 |
rs569039974 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176049065 | TAGTCCCAGCTACTC[C/G]GGAGGCTGAGGCAGG | 64326 |
rs569064546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176036161 | TCAAAATTTGCTAAA[A/G]TAGTGCTTAATGGGA | 64326 |
rs569065718 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:175997792 | AGGAACACTTTTACA[C/T]TGTTGGTGGGACTGT | 64326 |
rs569088937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176186473 | TTGAGCACAGCAGGC[A/G]AAGCTGCAGTGAACA | 64326 |
rs569091204 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176003300 | TCCCATTCTGTAGGT[A/T]GCCTGTTCACTCTGA | 64326 |
rs569111338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176139801 | GACACAGGGAACTAC[C/T]GGGGTGGGGGAAGGA | 64326 |
rs569120230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176129873 | AATTTAAAATCTAAC[A/G]AATAGTATGCTAACG | 64326 |
rs569136285 | in-del | -/TCTA | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176040321 | CCTTTTCCCTCCTTC[-/TCTA]TCTTTCTTTTCTGAG | 64326 |
rs569145764 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176090799 | ATGGCCAGAGACTCA[A/C/G]AAGAAAAGACCAAGA | 64326 |
rs569145773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176098752 | TACCTGGAATAATTT[A/G]GAATTCTATTTCATA | 64326 |
rs569147941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176180210 | TTAGCACAATATCCT[A/G]TTAAAAGAATTCAAA | 64326 |
rs569157489 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176152544 | CCTCCGCTCCCCAAG[A/G]TGAAGCAATTCTTCT | 64326 |
rs569164827 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992354 | GCATTTCCATCTGAG[A/G]TACCAGGTTCATCTC | 64326 |
rs569182866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176091332 | GCCTGGGCAACAGAG[C/T]GAGACTCCGTCTCAA | 64326 |
rs569189166 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176033368 | GGTGGTGGAGGCTGC[A/G]GTGAGCTGAGATCGT | 64326 |
rs569197273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176137650 | GAATTCAAATTAAGG[C/T]AGGCTTATTGTTCCA | 64326 |
rs569203606 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:175997479 | CTACAAAATGGGAGA[A/G]AATTTTCACAACCTA | 64326 |
rs569220828 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176019028 | AAAATTAGCCAGACA[C/T]GGTGGTACACACCTG | 64326 |
rs569233598 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176089494 | TTTGTGGTCCTAAAT[A/T]TGTATGGTATTTACC | 64326 |
rs569235456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176130512 | TTGATTAATTCTACG[A/G]AAAGTCTGAAATGGA | 64326 |
rs569238785 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176116863 | CAGCAAATATTTAAG[C/T]AATTTACCACTTCAA | 64326 |
rs569239663 | in-del | -/TTGGAATA | 0.0174175 | 0.0916809 | intron-variant | RFWD2 | GRCh38.p7 | 1:175949231 | CTATTAGAATTAACT[-/TTGGAATA]TTGGAATATTATGGG | 64326 |
rs569256549 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176128214 | CGCTGGCTCAAATAC[C/T]GGCTGAATGACTGAA | 64326 |
rs569262918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176088905 | GAGGCTGAGGCAGGA[A/G]AATCACTTGAACCCA | 64326 |
rs569269791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176082418 | GCAGATAATATAATG[C/T]ACAGTAAAGAATTTA | 64326 |
rs569271880 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176165883 | CAGATAAAGGAGAGA[A/G]CATGAAATAATTCAG | 64326 |
rs569294647 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175995103 | AACTCACTAAAAACC[A/G]CTCAACTACATGGAA | 64326 |
rs569296497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175966329 | CAAACACTTAAAAAC[C/T]TGTTTCATTATCACA | 64326 |
rs569313173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176172483 | GTACTGCTGTAGAAA[C/T]TGTGTGGACCAGTCC | 64326 |
rs569313927 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176120332 | GGCTGAGGCAGGAGA[A/C]TCTCTTGAACCCAGG | 64326 |
rs569350160 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176079555 | TCACTGTCTGGGTGA[C/T]GGAAATGTTAGGACC | 64326 |
rs569382785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176093593 | ACCTGTAATCCCAGC[A/G]CTTTGGGAGGCCGAG | 64326 |
rs569394988 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176001540 | AGATATTTCGTGGCA[A/C]AGTTATCTCAGGGTA | 64326 |
rs569395469 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176062056 | CCAGGCTGGAGTGCA[C/G]TGGTGCAATCTGGGC | 64326 |
rs569396432 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176040464 | TGAGACTACCTGTGC[A/G]CACCACCACGCCCAG | 64326 |
rs569396682 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175959359 | CATACTTAATGATAA[C/T]ATCTTTAAAAGCTTT | 64326 |
rs569421838 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176014318 | CTACTCTCATCAATG[C/G]AAGTTCAGAGAAAGT | 64326 |
rs569433223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176069496 | TATTTATCCTCCAAT[C/T]GAGTATTCCTCAGGT | 64326 |
rs569450430 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176166446 | GATCAAGCCTGTAAA[C/G]GCCACAAAATTAAAT | 64326 |
rs569459931 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176152322 | AAAAACAATTAAAAA[A/T]TGAAAAGATTCCTTC | 64326 |
rs569469869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176069136 | GCTGTAGTAAATCAG[A/G]ATTGCACGACTGCAC | 64326 |
rs569486389 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176053705 | ATTCCTTGTCTCCAA[C/T]AATCCTTCAAGGCCA | 64326 |
rs569500953 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992560 | ATACTGCGCTTTACC[A/G]ACAGGCTTAAAAAAT | 64326 |
rs569503908 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176036938 | TTGTAACAAATAAAA[C/T]GTATCGATTCCCTGA | 64326 |
rs569513829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176070264 | ATACATTCTTAAATA[C/T]TTCTTCTGCCTTGCC | 64326 |
rs569515661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176134243 | GATAAGATTCCATTA[A/G]ATCGTTATCCTAAAC | 64326 |
rs569530405 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176123115 | TCACACAGTAGAAAT[G/T]TTAAATTATCAGATG | 64326 |
rs569533024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176114500 | ACTATTTTTTCAAAT[A/G]AAGTGAATATACAAA | 64326 |
rs569539858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176027016 | TCCCAGGCAAACACC[A/G]ACATATGGTCACCCT | 64326 |
rs569554305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176127002 | CTTATTTTTCCTCCT[A/G]AGAATATATAACCAT | 64326 |
rs569572101 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176081454 | TCAGTTTTTCAGTTT[C/T]AATAAAAAATGTCTT | 64326 |
rs569573597 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176085280 | TTTTTACTATCAGTT[C/G]TATTAGTGGATATTA | 64326 |
rs569587463 | snp | C/T | 0.00438332 | 0.0466095 | downstream-variant-500B | RFWD2 | GRCh38.p7 | 1:175944641 | AATCTTTCTATCTAC[C/T]GTAAACAGTAAATTC | 64326 |
rs569593689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176075997 | AACAAGCGCAAAACT[C/T]CATCTCAAAAAAAAA | 64326 |
rs569607011 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176120776 | TGAAGAGGTAGCCAA[A/G]AGAAAACAATGGTTC | 64326 |
rs569632657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175947836 | AGAAAAGCCAAAAGA[A/G]ACAAAGACTGAAATA | 64326 |
rs569635754 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176111254 | TCTATGAAAAGTAAC[A/T]GCAAAATAAATGCTA | 64326 |
rs569645648 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176113675 | TAAATTTTATTTATT[G/T]CTAGCAGCAATAAAT | 64326 |
rs569646400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176169476 | CTTGGAGAAATCGCA[A/G]GTTCGGTTCTAGGCC | 64326 |
rs569646885 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176049251 | TTTCTTCTGCTGGTA[C/T]CCTGTTATTCAAGAC | 64326 |
rs569652857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175956342 | AAAAAGTAAACTTCA[A/G]TCCTTCTATCATACC | 64326 |
rs569658998 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176162364 | CGTCTTTAACAGTTA[C/T]GTAAAATAAATGGAA | 64326 |
rs569665059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176181974 | AAAGCTATTTAAGAA[A/G]GCAATGGGGCTTTCC | 64326 |
rs569666055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176030533 | AAGTTAGAAGGGTGG[C/T]AGGTCTTTTGTAATT | 64326 |
rs569672941 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176071930 | AGGCAAGGGAAAATA[A/C]ACAGGAAAACCAAGT | 64326 |
rs569674808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176063797 | AAACTTTCTGCTATA[C/T]ATACCAGAACTTGTT | 64326 |
rs569690122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176181608 | AGCACTTTGGGAGGC[C/T]GAGGCGGGCGGATCA | 64326 |
rs569700927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176072606 | TAAAAATCATATCCA[C/T]TCCTTAGAAAACAAG | 64326 |
rs569708529 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176170118 | TTCTAATTCTAGCTC[C/T]CTGGCTACTTCCTCC | 64326 |
rs569723228 | snp | A/C | 0.000215455 | 0.0103769 | intron-variant | RFWD2 | GRCh38.p7 | 1:176043838 | AAGAAATACAGTTAA[A/C]AGTTACTTTACATAA | 64326 |
rs569740753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176086476 | CATGATCCACCCGCC[C/T]CGGCCTCCCAAAGTG | 64326 |
rs569751531 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176203285 | GAGCTTGCAGTGAGC[C/T]GAGATCGCACCACTG | 64326 |
rs569761011 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176064719 | GGTTCACTGGTGTGA[A/T]CATGGCTCACTGCAG | 64326 |
rs569772342 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176188713 | TTGGGGAGCCACAAA[C/T]TGCACCCATATTAGA | 64326 |
rs569784513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176037278 | CAGGCATGGTGGCGG[A/G]TGCCCGTAGTCCCAG | 64326 |
rs569792221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176156291 | ACACTAAAATTACAA[C/T]AAAAAGAAGTACATG | 64326 |
rs569799161 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176156944 | GGCTCACACCAGTAA[A/T]TTCAGCACTTTTGGA | 64326 |
rs569809421 | in-del | -/G | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176057764 | GCTGCCACCCCATCT[-/G]GGAAGTGAGGAGCGT | 64326 |
rs569814588 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176137718 | TGAAAACAGTACCTT[A/C]TTATTAACTCATTTC | 64326 |
rs569817558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175990768 | TAAGTATATTCTGTT[C/T]GACCTAAATATAGCC | 64326 |
rs569847742 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176031101 | GAGCCTTCACAGAGA[G/T]TGTGGCCCTGCCAAC | 64326 |
rs569849480 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176108126 | TTTAGGTTTTCTGAG[A/C]TACATCAATTTTTTA | 64326 |
rs569860211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176024075 | CCAGCCTGGCCAAGA[C/T]GGTGAAACCCTGTCT | 64326 |
rs569861813 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175989129 | AGGGGGGAGGGTATA[C/T]AAAAAACTAGTATCT | 64326 |
rs569870318 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176140607 | TGGAAAGAAGAAATG[C/G]GCTAAATTCACTCTG | 64326 |
rs569895988 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176195209 | GAAGCTGAAGAGGCT[A/C]TATTAACATCAAAGT | 64326 |
rs569911380 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176066883 | TGATTGATCCCCTCC[A/G]CCCTTGGAACAGTTG | 64326 |
rs569921004 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176091446 | ATAAAAAAAGAGAGC[-/A]AGGAAACGAGCAAAT | 64326 |
rs569931158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175989122 | TGAGATAAGGGGGGA[A/G]GGTATATAAAAAACT | 64326 |
rs569938567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175999029 | TTTTATGTCTTTCCA[C/T]TTTAAAACACATCAG | 64326 |
rs569960561 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176192620 | GCTATGCTTTGCTCA[C/T]ATTTCAGAAGAGTAC | 64326 |
rs569969002 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175975904 | GAATGTAAAGTCTAC[A/C]TGATAATTGGGCTTT | 64326 |
rs569973263 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:176202584 | CCGTCTCTAATCCCC[A/G]CTGCTTGAGAGGCTA | 64326 |
rs569991571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175983163 | CAATTATTATTTGTC[A/G]AAAAGAAAAGAAACT | 64326 |
rs570013317 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175982518 | ATATATTTTCTTTTA[C/T]GATTTTCTTAATAAT | 64326 |
rs570020904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176008333 | CTGGGAGCTGTAGAC[C/T]GGAGCTGTTCCTATT | 64326 |
rs570025181 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176064439 | GAATCCCTGAGTATA[A/G]TTTGTCAAATGTAAT | 64326 |
rs570028926 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207235 | CGCCACCGCGGTCCC[C/T]GTAGCAGCCAACCCC | 64326 |
rs570029523 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175967876 | AATATTTCTTTTTTC[C/T]TTTTTTTTTGAGATG | 64326 |
rs570039936 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176014276 | CCCAACCAATTCCTA[A/C]ACAATCATCAGTGTG | 64326 |
rs570047645 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176112490 | AATATTTTGATAGAC[A/G]TATACAATGTGTAAT | 64326 |
rs570058739 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176029734 | TTTTAGAAATACTGA[G/T]ACAGTAACCTGTAGA | 64326 |
rs570074984 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176078035 | TTCCATAAGCATGAT[G/T]TGGAAGAATCGATAT | 64326 |
rs570080965 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176154397 | TCAACCTAAATGCCC[A/T]TTAATGGTAGATTAG | 64326 |
rs570103734 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175988661 | AACATAGCAAAACAC[A/C/T]GTCTCTACTAAAAAT | 64326 |
rs570109875 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176033793 | TTTATTTAAGCAATG[-/A]AAAAAAATAGCTGTT | 64326 |
rs570120906 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | RFWD2 | GRCh38.p7 | 1:176057746 | GATTGCAGCCTCTGC[A/C]CGGCTGCCACCCCAT | 64326 |
rs570155520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175972712 | CTCAGGTGATCTGCC[C/T]GCCTCGACCTCCCAA | 64326 |
rs570201377 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176050838 | AAGTAATTTGTCCAC[A/G]GATACACCAGATAAT | 64326 |
rs570218257 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176201655 | TTAATAGTCTTCCTA[A/T]CCTGTTTCATGATCA | 64326 |
rs570235252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176140987 | CTCAGAATCCCTTAC[A/G]AAGATAATAGATAGA | 64326 |
rs570235814 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176067708 | TCTGGTACACCAAGA[A/C]AAGAACCCCAGGATA | 64326 |
rs570255692 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176024325 | AAAAGTACTTGAAAA[A/G]CTGGTTTAATATTAT | 64326 |
rs570257614 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175960557 | CTAAAAGAAGAGTTT[-/A]AAGAAAGAGAAGCAA | 64326 |
rs570272567 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176005646 | GGTTGTTCAGTTTCC[A/G]TGAAGTTGAGCGGTT | 64326 |
rs570277663 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176187198 | GGCATGATCATGACT[C/G]ACTGCAACTTCGACC | 64326 |
rs570284451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176106572 | CTGGCAACACCCAGA[C/T]TGATTAACTGGCCCA | 64326 |
rs570284744 | snp | A/G | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176144625 | ATCCCAGACTTTAAA[A/G]AAGAACAGCAACTTA | 64326 |
rs570294350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176107081 | TGTTCTGTATATCCA[C/T]TGCCTGTAATCACAC | 64326 |
rs570295099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176089025 | AAATCTATTTAGGCC[A/G]GGCGTGGTGGCTCAC | 64326 |
rs570303494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176185022 | TTTAAGAAAGCTCTA[C/T]CATCGTTTTCCATCA | 64326 |
rs570306075 | snp | A/G | 0.000363666 | 0.0134796 | intron-variant | RFWD2 | GRCh38.p7 | 1:176043277 | ATGCTCCTGGAAGCA[A/G]AAAGAAGACAGTAGC | 64326 |
rs570311151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176057238 | TAAACATTTATATAG[C/T]TTGCTACATGAGTGA | 64326 |
rs570325440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175995618 | AGAATACTACAAACA[C/T]CTCTACACAAATAAA | 64326 |
rs570328555 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175979813 | TAGATATTAGAAGTA[A/T]CTCCCAACTCCACTT | 64326 |
rs570338025 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RFWD2 | GRCh38.p7 | 1:175966959 | CAATTTGAGATCTGG[A/G]GAATTGGGATTTCTT | 64326 |
rs570346432 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176170851 | GTCTGTTAGGCAAGG[C/T]GTGATAGCTCACGCC | 64326 |
rs570349963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176015100 | ACTGAAGAGTGTGCA[C/T]TGGCTGTGGTAAGAG | 64326 |
rs570350246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176147758 | TGTGGGAGGCCATGG[A/G]CCACCACATCAAAGG | 64326 |
rs570353831 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176197622 | ATTCACAGACCAGTA[A/T]CACTCACTAATAAAG | 64326 |
rs570375410 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176137455 | CCAGAAACACTATAC[C/T]AATTTAAATTCCTAA | 64326 |
rs570377777 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176191080 | ACCACCTGATTCTTT[C/G]TGATTTTATAATTTA | 64326 |
rs570393395 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176019212 | GTTCACACCTGTAAT[C/G]CCAGCACTTTGGGAG | 64326 |
rs570400911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176151531 | GGAGCGTATCTGCTA[C/T]GTGACATGAAATATG | 64326 |
rs570403760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175986395 | TTTGAGGCAACTCCA[C/T]TTTATAAAACCCAGT | 64326 |
rs570427215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175966408 | GATTACTTCACTTAA[C/T]CTGCATGGCAACCCA | 64326 |
rs570434630 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175995445 | CCCTTCAAAAAAATT[A/T]ATGAATCCAGGAGCT | 64326 |
rs570441442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176184416 | TTTTCAAATCCATCA[A/G]TAAGGCCTATTCTAA | 64326 |
rs570444553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176109759 | TTTTATTAGTATGCA[C/T]CAACACTGTCTTAGT | 64326 |
rs570445048 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176025448 | TATGAACAAGTTTTG[A/T]CTACATTTAGCAAAA | 64326 |
rs570488344 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176143228 | AACTTAAGACTCTAT[C/T]AAGACCAATCTTACG | 64326 |
rs570500583 | in-del | -/G | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176177524 | ACAGTATTTGTTTCT[-/G]GGTCATATAATTATG | 64326 |
rs570502499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176204753 | ACATGGTGAAACCCC[A/G]TCTCCATTAAAAATA | 64326 |
rs570510962 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176028540 | ACCAAAAAAAAAAAA[A/T]GAAATGAAATGAAAT | 64326 |
rs570514831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176001958 | GAGAAGTCATCAGAA[A/G]TATTAACATTAATCT | 64326 |
rs570515455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176204159 | AACTGGGAAATCTGA[A/G]TTCTCATTTTGTCCT | 64326 |
rs570520047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176115471 | AAATAAAAAATGGCT[A/G]AGCACGCTGGCTCAC | 64326 |
rs570524607 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | RFWD2 | GRCh38.p7 | 1:176144011 | ACATCATACCTAATG[C/G]TGACACGTTGAATGC | 64326 |
rs570531281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176026028 | AAGAATCCCAAAAGA[A/G]TTTTTCTAGAATTGG | 64326 |
rs570531336 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176158065 | AGATCTAAAAAATTC[A/C]AAGAACCCAATAACA | 64326 |
rs570532085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176047359 | ATCTACATTTTACAG[A/G]TGAGAAAATGAAGAT | 64326 |
rs570547051 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175992138 | GAATATGAGATGTTT[C/T]GATACAGGCATGCAA | 64326 |
rs570553605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176045590 | TAGAAGGAAAAAAAA[A/G]AAAAAAAAAGCAGAT | 64326 |
rs570559789 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176115518 | CTTGGAGAGGTCAAG[C/G]GGGGAGGATCACGAG | 64326 |
rs570572553 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176118131 | CTCTGGGCAAGTGAT[C/T]AATCTTATTTGAGCT | 64326 |
rs570581022 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175959381 | AAAAGCTTTCCCTTT[C/G]GTGAGGAACAAGTCA | 64326 |
rs570596871 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176009071 | GATATGCACACTACA[A/C]CTGGCACATGTGCAT | 64326 |
rs570597857 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176054951 | TGAAAATGCTGTATG[A/C]AGGTCAATAATGACC | 64326 |
rs570616630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176108973 | AAAAATTAGCTGGGC[A/G]CGGTGGTGCGCACCT | 64326 |
rs570633582 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176145483 | ATACACATATCCTAT[C/G]ACTCATCAATTCCAC | 64326 |
rs570640152 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176054597 | ATTCTGTGGTCTTTC[C/T]TGTCATTCCGAACGA | 64326 |
rs570642852 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175998934 | GGCACACTCAATTCC[A/G]CTCATGTTAATGATA | 64326 |
rs570667342 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176048459 | TTTGTACAACCTCAA[C/T]TGAACTGCTGCCTCA | 64326 |
rs570674719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175950464 | TCTAGCATAGAGATG[C/T]GGAAGTGGTACGTAC | 64326 |
rs570700812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176096937 | CATTTGTGGCCCGGG[A/G]TTCGATCCTGGCTTA | 64326 |
rs570709841 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176152293 | ATACATAATAGAGAG[C/T]GTGTGCAGTAAATAA | 64326 |
rs570718971 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176005670 | AGCGGTTTTGAGTGA[G/T]ATTCTTAATCCTGAG | 64326 |
rs570745014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176011324 | ATACTGCAGTTCTAT[C/T]TGACAGTTTTGATAG | 64326 |
rs570752808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176165078 | ACAAACAGATACCAA[A/G]CTCATAAGGATCCAA | 64326 |
rs570754180 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176082145 | AAATCATTGCTTTTC[A/G]GCACTGTGTCGTTTG | 64326 |
rs570757203 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176022678 | AAAGGTACAATGAAA[A/G]GCAATGAATTAAGCA | 64326 |
rs570782349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175965370 | TTTTTCTTTGTTCAA[C/T]GCCTTGTTAAGTGAT | 64326 |
rs570808472 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176006658 | AAATTCTTTTCTTTA[A/G/T]GAATGTTGAATATTG | 64326 |
rs570811415 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175949764 | AATTTAAAGCCGAAA[C/G]CTCCATCTCCTTCTG | 64326 |
rs570812924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176108668 | ATAACTATCAGATGA[C/T]TTCTTTGGTATCTAG | 64326 |
rs570814062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176182718 | CAAAGAGAACACTAC[C/T]GCCGAACAATGGCCT | 64326 |
rs570847358 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176190178 | CAGATTCGGATCTGT[C/G]TGCATTTTGAAATAT | 64326 |
rs570868869 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176150897 | TTAAAGGAAGAATTT[C/T]AAGAAAAGAGATGAA | 64326 |
rs570880111 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176139946 | TGTACTCCCTGAATC[A/G]AAAAGTTGAAATTAT | 64326 |
rs570881222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176101378 | TGTAACCCTTTTGAA[C/T]GCATCCTGAATCCCA | 64326 |
rs570907542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176052537 | TTCTCCCCATTTACT[A/G]CTATGTAAAATTCAG | 64326 |
rs570910064 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175971645 | CTCTTCCCATGAGCT[A/C]TTTCTGAGTTGTATC | 64326 |
rs570918680 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176140816 | GAGTTTGGTGCCACT[G/T]AGAAAAATAAATAAA | 64326 |
rs570920499 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176196136 | GATTAGAAAGGGAAA[C/T]TGATAAGATTAAGTG | 64326 |
rs570923178 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176189151 | AGAAAGACACATTAC[A/C]TGCAGAGGAATAAAG | 64326 |
rs570928740 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176058578 | GCTCATTAAGAGTCA[A/T]CACCACTCCCTAATC | 64326 |
rs570974913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176005211 | ATATCCCGTTTATCA[C/T]TTTTTATTGCATCTA | 64326 |
rs570984450 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176007596 | AGGTCTGTTGGAATA[C/T]CCTGCCGTGTGAGAT | 64326 |
rs570986320 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176014133 | AAGCATGCAGAATTT[G/T]ATTTGAGGTGAAAAT | 64326 |
rs570998510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176072969 | TCAAAGGAAAAGTGT[C/T]TTCTGAAACTTTACA | 64326 |
rs571007405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176183283 | TTCAGCATAAAATTA[C/T]GGGCCTGATTTCAAT | 64326 |
rs571034155 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176175477 | TCAGATTCTCATAAG[A/G]AGCGTGCAACTTAGA | 64326 |
rs571045339 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175958230 | CACACAAGAACAAAT[A/G]CGTATTTTATAAGTT | 64326 |
rs571046986 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175995072 | AGCGCAATCAAACTA[C/G]AACTCAGGATTAAGA | 64326 |
rs571047187 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175991512 | TAACAGTATACCTAG[C/G]CTACACTAAATTTAC | 64326 |
rs571058914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175991896 | ATAACAGTACCTTTT[C/T]CTGGAATGTCTCCTG | 64326 |
rs571062250 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175999583 | ACATGGGAATGCAGA[C/T]AGCTCTTTCATATAG | 64326 |
rs571075260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176177186 | ACTACTCATAGTTAT[C/T]GCTAGAGAACTGTGA | 64326 |
rs571077164 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176024196 | TCGGGGAGGCAGAGG[-/T]TGCAGTGAGCCAATA | 64326 |
rs571079985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176046392 | TTCTAAAGTAATTCG[A/G]TCTACAAGGATAAAA | 64326 |
rs571081576 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176176826 | AAAAGAGAAAAAAAA[G/T]ACAAAAGAAAATAAT | 64326 |
rs571090250 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176168585 | AGCAAGCTTTGGCAG[G/T]AGTGGAGTACACCTG | 64326 |
rs571091598 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176129021 | CAATGACCAGAGATT[A/G]GTATAGTTGCATAGA | 64326 |
rs571100654 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176002462 | TGCACCCACTAACTC[A/G]TCACCTAGCATTAGG | 64326 |
rs571129595 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176087581 | CACCAGTTAGAATGG[C/T]AATCATTAAAAAGTC | 64326 |
rs571131425 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176080671 | CAGCCCTGATGAGAC[A/G]GACAAATGTCTTAAA | 64326 |
rs571131813 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176096090 | CTCATCCTTCTAGGT[G/T]TCCACAAGCCTAATC | 64326 |
rs571139063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176029793 | TTCCAATAAATACCA[C/T]TTCTATGAAACGGGA | 64326 |
rs571139650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176031975 | ATTCAGTTCCAGTGT[A/G]CAAGGTTTATGTTTC | 64326 |
rs571151898 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176162251 | TCAATAAATACTCCC[C/T]TTATGTTTAACCTCA | 64326 |
rs571158909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176001293 | TTCATCGAATGAACC[C/T]CTAGGCATCAAGTAT | 64326 |
rs571168243 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176088021 | AGAAAACCAAACACC[A/G]TATGTTCTCACTCAT | 64326 |
rs571175121 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RFWD2 | GRCh38.p7 | 1:176003568 | TCAGCTTTCTACATA[C/T]GGCTAGCCAGTTTTC | 64326 |
rs571179990 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176037421 | CAAAAAAAAAAAGTA[C/T]AAGAAAAAAAAAAAC | 64326 |
rs571189533 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175994818 | TTAACACGCCACTGT[A/C]AACATTAGACAGATC | 64326 |
rs571195192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176049802 | TAATACAAAACAGAT[A/G]ACCTCTTATATTAAC | 64326 |
rs571246229 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:175997877 | CTAGAAATACCATTT[C/G]ACCCAGCCATCCCAT | 64326 |
rs571260245 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176187010 | ACAGTACGTGTCATG[C/T]CACATAATGTGTTCT | 64326 |
rs571292713 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175961915 | AATAAATTTGAAAAA[A/C]AAAAATGGTTTTGGA | 64326 |
rs571293739 | snp | C/T | 0.0894459 | 0.191631 | intron-variant | RFWD2 | GRCh38.p7 | 1:176002955 | CCACAATGGTTGAAC[C/T]AGTTTACAGTCCCAC | 64326 |
rs571303224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176147093 | TTCAAAGTTTGAATG[C/T]CAAAAGAAGCAATTT | 64326 |
rs571309045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992804 | TGCCTCTGTAGGCTC[C/T]ACCTCTGGGGGCAGG | 64326 |
rs571312982 | in-del | -/AAGGACAAAATGAA | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175975745 | AAAATAATGATTTGG[-/AAGGACAAAATGAA]AAGGAAACACAAGTA | 64326 |
rs571314296 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175946872 | GGGCTCTATCTACTG[A/G]AAGCCCTGTGGGAGA | 64326 |
rs571326979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176116945 | ACAAGGCAGATGTCT[A/G]TATAGATTTACTTGT | 64326 |
rs571350216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176056568 | CTTTCTAGCCTGAAT[C/T]AAACCTTACTTTCAA | 64326 |
rs571376372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176089654 | ATATTTTAAAGCACT[A/G]CTTCACTCTGAGACC | 64326 |
rs571383076 | snp | A/T | 0.000727215 | 0.0190546 | intron-variant, nc-transcript-variant, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175968494 | CAATCTGTAGACAAA[A/T]GGCATTTTTTCATTT | 64326 |
rs571387395 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176143932 | TTTAAAAATTCTCTT[A/G]GCAAACTGGGTAAAA | 64326 |
rs571389593 | in-del | -/AGT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176114050 | TCATCAGTCACAGGG[-/AGT]AGTAGCCTTGTCTGA | 64326 |
rs571395358 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176169198 | AAAGGAAATGGAATC[C/G]TCGTCATAGTAATAT | 64326 |
rs571416672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176082482 | AACTGTTTGCATGAC[A/G]AAATTTATGTAACAA | 64326 |
rs571421740 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176068500 | TGAAAGGGTAAGAAC[A/G]ACTAACATTTACGTA | 64326 |
rs571453982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176072064 | CTTTATTTTGAATCA[C/T]GTATGTTTTGAATTA | 64326 |
rs571472329 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176180872 | TAGCCAAGAGTCTCA[A/C]AAGGCAATTTGACAC | 64326 |
rs571476697 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175998788 | GTGTATTCAAAAAAC[A/C]TAAGGTAATCCTAGG | 64326 |
rs571489453 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207565 | CGCAGGCGCGCGCCG[A/G]GCGCGGACGCTCACG | 64326 |
rs571491961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176150393 | ATAGAATCATGAAGA[C/T]TGAAATTTTTTCTTG | 64326 |
rs571504197 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176208629 | AGGAGGTAAAGGAAG[A/G]CAAAGGTTTTTAAAA | 64326 |
rs571509112 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175954244 | AAGATAATAAAAATG[C/G]AACATATCAAAATTT | 64326 |
rs571539616 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:175946126 | GAGAGTATAGAAAGC[C/T]ACTTAAATCAGATAT | 64326 |
rs571546489 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RFWD2 | GRCh38.p7 | 1:176076085 | GAGGCAGAACACTAA[C/T]GAAATTCTGGACTTA | 64326 |
rs571549305 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176125637 | TATAGCTATATAGTA[C/T]AATGTAAAATCAGGT | 64326 |
rs571554086 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176148298 | CCCAGAACATAGCAC[A/G]TAACAGACAATTTAC | 64326 |
rs571554290 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175987464 | AGTAGAACCAGAAAT[A/G]TATTATAAGAATCTT | 64326 |
rs571570563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175987965 | CCAAAATTGGAAATA[C/T]TACTAACAGAACTTA | 64326 |
rs571581597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176027251 | CAATATAGCTTAATA[A/G]TAGCTTAATTGTTTA | 64326 |
rs571582325 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176199113 | ATGAGGTCCAGGGAT[C/T]GAGACCAACCCGGCC | 64326 |
rs571589102 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:176191956 | TAAAATATTTTTTAA[A/G]TAAGGATTCTAAATA | 64326 |
rs571604146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175993364 | AAAGGAACGCAGCTC[C/T]TCACCAGCAACGGAA | 64326 |
rs571630859 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176122668 | GGTTACAAAAAGTAA[C/G]AGTTACATAATGCAT | 64326 |
rs571634405 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176124705 | TTCCAAATCTTGGCT[A/T]TTGTGAACAGTGCTG | 64326 |
rs571648375 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176076402 | GAAATTAAGGCAGGA[A/T]TAACAAAATTCTTTG | 64326 |
rs571648516 | in-del | -/TTATT | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176011979 | TGTACTTTTTAATCA[-/TTATT]TTAGAGTGTACTCCT | 64326 |
rs571649608 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176166595 | TACTACTGTATCAGA[G/T]TTTTCATGGAGTTAC | 64326 |
rs571649932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176130577 | TATTTTTTTAAAAAA[C/T]ATACCTCACCTCAAT | 64326 |
rs571652483 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176068189 | AAATATAAATATTTC[C/T]TATTAGAAATGTCTT | 64326 |
rs571666339 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176172628 | CTAAGAGGAAATCTG[A/C]AATCATTTTAAAAGG | 64326 |
rs571692004 | in-del | -/TTATCT | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176059291 | AACCTAAGAAAAAAA[-/TTATCT]TTGTATGGCAATAAA | 64326 |
rs571695650 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175989191 | GTGCACAATACAGAC[C/T]AGAAACCACACTACT | 64326 |
rs571709497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176167107 | AAATCTCTTAAAATG[C/T]AAGGTATATACACTG | 64326 |
rs571733158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176107736 | AGCCACCATTTTAAT[C/T]GAGTGATCAAAGTTA | 64326 |
rs571739750 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175996132 | CAGCATATAAACAGA[A/G]CCAAAGACAAAATCC | 64326 |
rs571748393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176131297 | CTAGATGAGGTGATG[C/T]TAAGGATCTAAACAA | 64326 |
rs571763777 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176083409 | AACAGAAACCATAAA[G/T]AAAACAATAAAACTA | 64326 |
rs571773542 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176202792 | ATGCATAGTCCATTA[C/G]AGTATTTAACATCTG | 64326 |
rs571788853 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175981829 | AAACAAGCAAAGAAC[C/G]TGAATAAACATTTCT | 64326 |
rs571794496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175978048 | ACTTTTTAGCATGGT[A/G]AGATTACAATAAAAG | 64326 |
rs571795448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176146189 | GGGAATCATTCAAAT[A/G]CTGGTACAAATTTGC | 64326 |
rs571803001 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176208167 | ATAGGCGGGCGCGGT[A/G]GCTCATGCCTGTCAT | 64326 |
rs571806954 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176112969 | CCTTTCATCTGCTGA[G/T]GGACACTTAGGTTGA | 64326 |
rs571812122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175981077 | CCAGTCTCTAGATAA[A/G]TCAATGTTAATAAAA | 64326 |
rs571823771 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176199924 | TTTATGCAAATTATA[A/G]CTTAGTAAAGCTAAT | 64326 |
rs571832760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176063076 | TTTTTTTTTTGAGAC[A/G]GAGTCTCGCTCTGTC | 64326 |
rs571844480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175990179 | TAAAATCCTTTTACA[C/T]TTCCTTTGTTATTTC | 64326 |
rs571846577 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175945261 | ATTTACCAATAGAAA[A/C]GCAAATTTAAAAAAC | 64326 |
rs571852072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175974503 | AAGCAATCATTAAAC[C/T]AGACTCAGGTACGAC | 64326 |
rs571879961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176192784 | ATACATTTCATTAGA[C/T]AGTATCCCCATCCCA | 64326 |
rs571889404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175966481 | ACATAGTCTTAGACT[C/T]AATAACTTGTCCAAA | 64326 |
rs571895507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176199285 | TCGTGCCACTGCACT[C/T]CAGCTGGGGCGACAG | 64326 |
rs571897239 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176065744 | ACGGAGTCTTGCTCC[C/G]TTGCCTAGGTTGGAG | 64326 |
rs571910994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176020890 | TCTAAAGTATTTACA[A/G]TGAGTTATAAAATAC | 64326 |
rs571918483 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176063692 | GTATGATATAGCTAA[G/T]TTGCCTAAACATAGG | 64326 |
rs571928785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176096963 | GCTTAGGGAATGAGT[C/T]CTTTTTGGTTTGATA | 64326 |
rs571931666 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176153121 | ACATGTCTGCTCACA[C/G]GACATCACTCCAGTT | 64326 |
rs571933397 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176070429 | GCACTTTGGGAGGCC[A/G]AGGTGGGTGGATCCC | 64326 |
rs571951675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176134713 | ATTTAGATTTTTGAA[C/T]GTCATCTGACTTTAA | 64326 |
rs571956266 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207101 | GAGCCGGAGGTGGGG[C/T]TGAGGAACAATAAAG | 64326 |
rs571970111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176108343 | GTAGCACTATTTCTG[C/T]AACTATTCTATTATG | 64326 |
rs571975082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176016484 | TGAGAAGAATTTCTA[C/T]GTAAGGGTAGGAGCA | 64326 |
rs571984938 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176135415 | ATTATACTATGTGAA[C/T]AGTGAACTAGCATAT | 64326 |
rs572014809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176009216 | AGAGTCTGACACAGC[C/T]GTGATACTGCATCTG | 64326 |
rs572014857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176005007 | TTGGTTGGTAAGCTA[C/T]TGATTCTTGCCACAA | 64326 |
rs572030466 | in-del | -/TTAGAA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175950357 | TACAAAAAAAGTTAT[-/TTAGAA]TTAAACTATCAGATA | 64326 |
rs572041458 | in-del | -/TA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176133180 | ATGTACACACATACG[-/TA]TATATACGTACGTAT | 64326 |
rs572044409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176120375 | CAGTGAGCCGAGATC[A/G]CACCACTGCACTCCA | 64326 |
rs572060854 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176023599 | GGCATATGCCTGTAA[C/T]CCCAGCTACTTGGGA | 64326 |
rs572083630 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176166866 | TGCCTGAGCTCAGGA[A/G]TTCGAGGCTGCAGTG | 64326 |
rs572091886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175968853 | CCTTGTCACACTGCA[C/T]TCAAATATTCTCTCT | 64326 |
rs572111098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176057984 | CGTCTCTGCCTGGCC[A/G]CCCCGTCTGAGAGGT | 64326 |
rs572119197 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176109443 | TATTAATTACTTTTT[A/G]GTAGATTTTAAATTT | 64326 |
rs572120177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176187257 | CAGCCTCTCAAGTAG[C/T]TGGGACTACAGGTGC | 64326 |
rs572121324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176015762 | AAATAGTAATGAAAA[A/G]GAACAGACTAGATCA | 64326 |
rs572124508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176030666 | AATATAACTGTCTGA[A/G]CTACAAGGGTAACTA | 64326 |
rs572130799 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176162621 | GAAACTTTACTTTCT[C/G]AAGATTTTGAACACT | 64326 |
rs572141652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175983471 | AGCCATGTGGAACTG[C/T]GAGTCCAATAAACCT | 64326 |
rs572153781 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175952187 | AGCACTTTGGGAGGC[C/T]ATGGCAGGCGGATCG | 64326 |
rs572158584 | in-del | -/A/GA | 0.00151363 | 0.0274686 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176176023 | TATTAGTAGGGGGGG[-/A/GA]AAAAAAAAGGCTTAA | 64326 |
rs572172439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175999881 | GAGCACTTTTACATA[C/T]ACCAGTTTGCCATTT | 64326 |
rs572179352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175968238 | AATAAGCAAATAACA[C/T]CTATTTTCAAAACTC | 64326 |
rs572192165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176163101 | CATAGATATCGAAAA[C/T]ATATTATAATGTTCC | 64326 |
rs572230184 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176195897 | AAAATCGGGGACGGA[A/G]GGGGTTAGGAGCTGA | 64326 |
rs572235157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176052724 | CTCTGTAGGCAACCA[A/G]TAATTTCAACTTGTG | 64326 |
rs572249564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176186785 | GTGTTGAAACGGACT[A/G]GGGTGGTAGTAGTTG | 64326 |
rs572255279 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176101085 | TCTAGGGAATTCAAA[G/T]GCTACTGACAGCAGG | 64326 |
rs572273212 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176030984 | GAAGGCCATGTGTGA[A/G]GAGAGCCAAGACCAG | 64326 |
rs572280846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176182340 | TTTCAGAACCAGAAG[C/T]AGAATCCTGGTCTAA | 64326 |
rs572295090 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176079352 | GTGAAGCTAGAGGCC[A/G]TTATCCTAAGTGAAT | 64326 |
rs572298547 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:176078378 | CTTTGACAAAATCAA[C/T]AAAAACAAGCAATGG | 64326 |
rs572313585 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176192876 | TTGATTTTTAAGATT[A/C]ATTTTTTTAAAAAGT | 64326 |
rs572327853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175989676 | AAGGGGTCAAAATAA[C/T]TGGAAACTTAAAAAT | 64326 |
rs572335408 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176079135 | AGCAATCCCATTAGT[A/C]GGTATACGCACAAAA | 64326 |
rs572343580 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176142097 | AATAAATAAATGATA[C/G]AGTAGTGAGGGGACA | 64326 |
rs572345021 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176093978 | TAGTAAGCTGAGATT[C/G]TGCCACTGCACTCCA | 64326 |
rs572346530 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176058745 | CGAGAAACACCCAAG[A/G]ATGATCAATAAAAAA | 64326 |
rs572348336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176051894 | TGTTTTTAGCCAAGG[A/G]TTATTGCAAAAAAAT | 64326 |
rs572354172 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176035224 | TAAAATTAATGGAAA[A/G]ATAGAAGTACTCAGA | 64326 |
rs572354578 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176188279 | AAATAGGTAGAATAG[A/C]ATAAAGAAAGAAGGG | 64326 |
rs572359233 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175963028 | AACATGAATGTTACA[G/T]GTGGGTGTTTTCTGT | 64326 |
rs572367481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176085519 | TTTGTTGGCTACATA[C/T]TCATAGCTGAATTTC | 64326 |
rs572368049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176050215 | CAACAGCTGAAATAC[A/G]TAATTCAGCTGTAGG | 64326 |
rs572385936 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176133726 | GTAACAAAGATCTGG[A/C]AACAATATATACAAA | 64326 |
rs572392360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176194665 | AACAAAGGCAGATTG[C/T]CATACTAAATAAAAA | 64326 |
rs572420984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175975259 | ATTTACTAATATTAT[C/T]CCCCACCCCAAAACC | 64326 |
rs572423932 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176140471 | TATTAAATTTGAGGT[G/T]TTTCCATTTTAAGAT | 64326 |
rs572429780 | in-del | -/AGAC | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176189619 | GCAGAAGGAATATGA[-/AGAC]AGACAGAAACTAGGA | 64326 |
rs572430125 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175982167 | TAGCAATTACACTTC[C/T]GAGCATTGAATCCCA | 64326 |
rs572482145 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176166696 | AATCCCATTATTTAG[G/T]GAGGCTGAGGCAGGC | 64326 |
rs572485376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176193656 | GCTGATACATGTCAC[A/G]ACATGGATGAGCCTT | 64326 |
rs572488999 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176005762 | TTGCTGAGAGCTTTA[C/G]TTCCAACTATGTGGT | 64326 |
rs572507417 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175993724 | AAATGAGCAAAGCCT[A/C]CAAGAAATATGCGAC | 64326 |
rs572513203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176184464 | AAATTATGCGCCAGC[C/T]ATTATGTTAACAGCC | 64326 |
rs572520312 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176147405 | ACCTAGCTCCTCAGA[A/C]TTTCTTGTGTAATTA | 64326 |
rs572542264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176175495 | CGTGCAACTTAGATC[C/T]CTTGCATGTGCAGTT | 64326 |
rs572542671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176099340 | TAAGAGTTAACTAAA[C/T]GAACTGAACTCACCA | 64326 |
rs572549821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175959205 | CAATATTTGAAAGAA[A/G]AATATTATATCATGT | 64326 |
rs572562768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176126402 | TCCTTCTATAACCAG[C/T]TCATTGAAGGTTTTT | 64326 |
rs572563696 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176007656 | CCAGTTAGGCTGCTC[A/G]GGGGTCAGGGGTCAG | 64326 |
rs572573185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176125923 | CTTTATAGTTTTCAT[C/T]ATAGATATCTTTCAC | 64326 |
rs572577528 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176114510 | CAAATAAAGTGAATA[C/T]ACAAATAAATGTTCA | 64326 |
rs572582362 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176054207 | CTCTGTCACCCAGGC[A/T]GGGGTGCAGTGGGCA | 64326 |
rs572603831 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176092168 | CTAGTGTTATGCAAG[C/T]AACACTAGTTTATAT | 64326 |
rs572626855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176072326 | TTTTCATTCATTCAT[A/G]CATTCATTTAACAAA | 64326 |
rs572653067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176037061 | CTTCAAACAAAGAAA[A/G]CTACACGCCCAGAAA | 64326 |
rs572677969 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175998474 | AATAATAATAAAATT[A/T]AAAAAAGAGAAAAAA | 64326 |
rs572689527 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175999082 | CAGTTTTCAACCCAT[C/G]ATGGTATGAGAAAGT | 64326 |
rs572704805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175946529 | TACTCTCAGAAACAC[A/G]TACTCCACCAAAAGG | 64326 |
rs572719663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175986772 | CATTGCTCTATTACT[A/G]TGCATTTCAATCACT | 64326 |
rs572731252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176174860 | CCTGAAAATTATTCT[C/T]TAGCTTATTATTCAT | 64326 |
rs572738512 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:176036621 | TTTGACTTTACAATG[G/T]TGAGAATGCAATGTG | 64326 |
rs572742442 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176089671 | TTCACTCTGAGACCT[-/A]AACTCTGAGTTTTTT | 64326 |
rs572765203 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176081497 | GATACTGTCTCTTTC[C/T]ACTGTGAATTCTCAC | 64326 |
rs572786459 | in-del | -/GG | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176009888 | TACTTGGGGGGGGGG[-/GG]TCCGCAATAATTTTC | 64326 |
rs572832193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176136236 | CCAAGAAAACTGAGC[A/G]ATTTTTTTTGTCAGT | 64326 |
rs572837294 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176123958 | AAGATCTACCTCAAA[C/G]CTAATCAATCAGATT | 64326 |
rs572843392 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176047553 | AAGGTTTAAAATCTA[C/T]GTGTATGAATGTATC | 64326 |
rs572844482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176001681 | TATACCGATATGATT[A/G]TCTTAACCAGTTCTC | 64326 |
rs572868220 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176144435 | TAAGGCTATTTTAAA[C/G]ATCTAAATATAGAGG | 64326 |
rs572884156 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176196069 | AGAAATCACAAGGGA[A/C]ATGAGAAGTATTATG | 64326 |
rs572886225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176010696 | TATAAAGGGAATCTG[C/T]CTCTCTTATTTCAGT | 64326 |
rs572890800 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176096469 | ACACAGGGCGGGAAT[C/G]AGCCACAGCCACTGT | 64326 |
rs572925584 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176103037 | CTCTGGGCTCAAGCA[G/T]AGCTGGCTCTGCATG | 64326 |
rs572929395 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176094905 | CTTAATATAAAATAG[C/T]GGAGTACAAAAGCAA | 64326 |
rs572936672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176024400 | TCACAATCAACCTCA[A/G]CAGAGGCAAAAAAAA | 64326 |
rs572936899 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176032130 | AATGAGGATGTGCAA[A/C]TATGAGTAAGTTTCA | 64326 |
rs572944521 | in-del | -/AG | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176170598 | TAAATCACGCTGAAA[-/AG]AGATATGCTGTCTTC | 64326 |
rs572950367 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176166118 | AAGATCAAGCCTGTA[C/T]TTATTTATTTTATTT | 64326 |
rs572956436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176116217 | ATCCATCTAGATCTA[C/T]AGTAAGTACAAAAAT | 64326 |
rs572956575 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176011558 | TATGCTTATCATACC[A/G]TCTTAACAATCAAAT | 64326 |
rs572967143 | in-del | -/C/CC/CT | 0.0150797 | 0.0856793 | intron-variant | RFWD2 | GRCh38.p7 | 1:176112771 | CCTCCATGAGATCCA[-/C/CC/CT]CTTTTTTTTGGCTCC | 64326 |
rs572979368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176135276 | AAGTTAAGAGACAAG[C/T]CTTTTCCATGGTACA | 64326 |
rs572979732 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176199847 | TCATTAGGGTGGTGA[C/T]TGCACAGGTGTATTC | 64326 |
rs572983871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176069143 | TAAATCAGGATTGCA[C/T]GACTGCACTCCAGCC | 64326 |
rs573004455 | in-del | -/TATT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176069454 | GCCACAAGCATTTAC[-/TATT]TATTTTCTACCTTGA | 64326 |
rs573023492 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176031508 | GACGAAAATTCCCTT[C/T]GAAAGAAAAAGTAAA | 64326 |
rs573032111 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176103689 | AATCTGTATTTCTTA[C/T]AACTGCATGTAAATC | 64326 |
rs573034844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176086448 | AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTCAT | 64326 |
rs573049437 | in-del | -/TTCCT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176174438 | TGTTCTTTTCCTAAG[-/TTCCT]TCTCCAAGTTTGCCA | 64326 |
rs573071290 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175992037 | TCTTTATCAAGTATT[A/G]TGTAGTATACGTAAT | 64326 |
rs573085024 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176158143 | TAATCAAAACACTTA[C/T]ACCCATAAAAAGAGT | 64326 |
rs573113344 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175952069 | CATAAAGAGAAAGAT[C/G/T]GCCAATTTCCCATCA | 64326 |
rs573121885 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176158914 | CAAAGTGCTAGGGTT[-/A]ACAGGCGTAAGCCAC | 64326 |
rs573136191 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:175995694 | CTCCCAAGACTAAAC[C/G]AGGAAGAAATTGAAT | 64326 |
rs573150318 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175994861 | AGTCAACAAGGATAT[A/C]CAGGAATTGAACTCA | 64326 |
rs573153576 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176170882 | TGTAATCCCAGCACT[C/T]TGGGAGGCCGAGACT | 64326 |
rs573168687 | in-del | -/AAAA | 0.00244319 | 0.0348658 | intron-variant | RFWD2 | GRCh38.p7 | 1:175950215 | AATACTTTATGTGTT[-/AAAA]AAAAAAAAAGTCAAC | 64326 |
rs573183227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176073648 | CATCTTCTACTTATG[A/G]GAGTGAACTTCACTG | 64326 |
rs573194644 | in-del | -/G | 0.00121237 | 0.0245909 | intron-variant | RFWD2 | GRCh38.p7 | 1:175956483 | GGATGCAAAAAACAT[-/G]TACAATAAAGGAAAA | 64326 |
rs573198352 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176025078 | ATTCAGTGTTAGAAA[A/G]AGCATAAGCACCAAT | 64326 |
rs573218632 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176051011 | TACATTATATATAGT[A/G]ATAATAACACATAAT | 64326 |
rs573219224 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176038531 | GTACAAGTAAAAGAA[G/T]AGATAGGGCTGGGCA | 64326 |
rs573220042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175949929 | CTGACTTCTGATGGG[A/G]GCAAAACTAGGAAAA | 64326 |
rs573232815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175991118 | GCTGAACAGTAAGTA[C/T]AATAATACATACTTA | 64326 |
rs573235765 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176000389 | GTTCTTGGCAAGTTT[C/G]TCAAAAATGAGTTCA | 64326 |
rs573242160 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176099917 | CAAACTGATGGCTGG[A/G]CTTGGCTTTAAAAGG | 64326 |
rs573262806 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176176363 | CATATTATTGGCCTG[C/T]GAATACCCTTAATAC | 64326 |
rs573263144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176080708 | AAACTAATTATAATG[C/T]TAAATCAAGAAGAAA | 64326 |
rs573276048 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175949160 | GAGACTCCAGCAAGG[C/G]TCCGTCTCAAAAAAA | 64326 |
rs573278217 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176097915 | GGCCTAAAGGAAGAT[-/A]AAACACTTTGATCAA | 64326 |
rs573278304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175981760 | ATTTATCAGTTAGGG[A/G]GTTATAAGGAACTCC | 64326 |
rs573289443 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176023466 | GCTCACGCCTGTAAT[C/T]CCAGCACTTTGGGAG | 64326 |
rs573294057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175984673 | AGACAATGCCAGCTC[A/G]TTAAAGCAGCCAGGA | 64326 |
rs573302523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175994586 | CAAAAAAAGGCAGGG[A/G]TTGCAATCCTAGTCT | 64326 |
rs573324339 | in-del | -/AGAA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176151293 | GAAGGAAGGAAGGAG[-/AGAA]AGAAAGAAAGGAGAG | 64326 |
rs573351180 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RFWD2 | GRCh38.p7 | 1:175979061 | ACCATTTAGGTTTCT[C/T]GGTTAGGATGTATAA | 64326 |
rs573376085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176087638 | GTGAAGAAACAGGAA[C/T]GCTTTTACACTGTTG | 64326 |
rs573376097 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176080076 | TCAGTAATCATGGGT[C/T]GAAGAGAAAAATCAA | 64326 |
rs573376945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176124900 | CACCATACAAGGGTT[C/T]CCTTTTCTCCACATC | 64326 |
rs573382385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176132248 | TCCTGCTCAACACTA[C/T]CCCATAACTTTCCAT | 64326 |
rs573386099 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176009880 | GTTTAGGTTACTTGG[C/G]GGGGGGGGGTCCGCA | 64326 |
rs573397446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175979906 | GCTTGAAGTGTTGTA[C/T]CGTTCATTACAAAAA | 64326 |
rs573413814 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176018890 | TTAATTCCAGGCCAG[A/T]CAAGGTGGTTCACGC | 64326 |
rs573424977 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176017620 | ACCTCCGCCTCCTGG[A/G]TTCAAGCTATTGTCA | 64326 |
rs573431792 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176204206 | AACAAAATTACTTCT[C/G]TGTGCCTCAATGAGA | 64326 |
rs573449049 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207538 | CGGGCGGAAACTCTC[A/G]AAAAGCGACTGCGCA | 64326 |
rs573467627 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176018132 | AAACCTTAAAGATGC[A/T]CTAATGTTAGCTATT | 64326 |
rs573475939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176067377 | CTGGCCCACCGCGCC[C/T]CCATCCTGCACCTAT | 64326 |
rs573488858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176102455 | TCCAAAGTTCTGAAA[C/T]TGCCACTGCAAAATT | 64326 |
rs573502710 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176109244 | GCTTTCTTATATGTA[G/T]GGTAGACTTCTTTCT | 64326 |
rs573521173 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176118108 | ACCCATAGAAGTGAA[G/T]AACCTGACTCTGGGC | 64326 |
rs573527170 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176147941 | TTCTCGCCCTGTTGC[C/T]CAGGCTGGAGTGCAG | 64326 |
rs573547918 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176070952 | GCTCCCATGTGCAAC[C/G]ACTCCTGCTTCTGTC | 64326 |
rs573549960 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176121061 | GATTTTTTTTGCTAT[-/A]AACGTAAAAGAGAGA | 64326 |
rs573573650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175987255 | ACTAATTAGAAATCA[C/T]GTAAGAAAAGGATTC | 64326 |
rs573576218 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:175988780 | AGATGCTGCAGTGAG[C/T]GGAGATCACACCACT | 64326 |
rs573596082 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175946338 | TGCTCATTTCACCTC[G/T]GTAGAATGTTTAGGC | 64326 |
rs573611405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175985333 | GTGCCCTAGTTATTG[C/T]AGTTACAAAACTAAA | 64326 |
rs573637805 | snp | C/T | 1.6522e-05 | 0.00287414 | missense | RFWD2 | GRCh38.p7 | 1:175988384 | ATGGTTTCCCTACAT[C/T]CCACAGTTTTAGCTG | 64326 |
rs573645584 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176035481 | ACTAGCAGTAGTTTG[A/G]TAAGTATGTGACAAA | 64326 |
rs573656665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176085127 | TCTTTGCATATGTTA[C/T]TTCCTCTACTTTGAA | 64326 |
rs573661833 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175997591 | AAAGTGGGCGAAGGG[A/C]ATGAACAGACACTTC | 64326 |
rs573670317 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176077780 | CCAAAAGGCTCCTGG[A/G]ACTGATAGACAAATT | 64326 |
rs573670654 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176089085 | AGGTGTGTGGATCAC[A/G]AGATCAGAAGTTCAA | 64326 |
rs573677154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176036417 | TAAACAATAAATAAA[C/T]GAGAGGACACAAAAT | 64326 |
rs573679353 | in-del | -/A | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:176198581 | AAAATTAAAAATAAT[-/A]AAAATCAATTTGGAC | 64326 |
rs573684718 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176032779 | ACATAAATGAAGCCT[-/G]GGAACAAGGTAGGTG | 64326 |
rs573692199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175981148 | AAGCATATCCTCTAA[A/G]GTTTTCTTTAGTGTA | 64326 |
rs573706882 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176063352 | GGCATGAGCCACCGC[A/G]CCTGGCCCGAAAATG | 64326 |
rs573724241 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176015468 | CTATCCAAAATAACC[A/C]CTTCAATTTTTGAGG | 64326 |
rs573725120 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175993032 | ACACCGCCGGGTACT[A/C]CTCTGAGACAAAACT | 64326 |
rs573752120 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176180424 | GATACTAAGAGAAGG[A/G]TAAGTATCTAGATTA | 64326 |
rs573752251 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176173491 | AACAAACAAACAAAA[A/G]TAGCCAGGTATGGTG | 64326 |
rs573777169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176205772 | CTGTATCATTCAAGA[C/T]GCCAACTATGACGAC | 64326 |
rs573778166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175975472 | TGGAGTGCAGTGCCA[C/T]GATCTCGGCTCACTG | 64326 |
rs573782595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176194518 | TGGCATGAGCCTATA[A/G]TCCCAGCTACTAGGG | 64326 |
rs573783733 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176077061 | TAGAGGTACAAAGAA[C/T]TGATACCAATCCTGC | 64326 |
rs573828342 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:175987539 | TGGCAACACTTACAC[A/T]GGCAGATTTTCATAG | 64326 |
rs573841527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176161553 | CAGTGAGCTATGACT[A/G]TACCACTGCACTCCA | 64326 |
rs573853063 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176002995 | AAAAGTGTTCCTATT[C/T]CTCCACATCCTCTCC | 64326 |
rs573887094 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176014526 | ATTTCTTTAAGGCTA[A/T]ATGGACATTTAAAAA | 64326 |
rs573888821 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175976165 | CTCTGAAGTTGCAAG[C/G]CTAATTTGTTAATTG | 64326 |
rs573894581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176193724 | CCATATATTATATGA[C/T]TGCATTTATATGAAG | 64326 |
rs573894987 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176106782 | AGCACAGCGGCTCTG[A/C]ATGAATTACTTTATC | 64326 |
rs573895400 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176064008 | TCTGAAAATATGACA[G/T]AAGTTTAATCAAGTG | 64326 |
rs573902528 | in-del | -/GGCC | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176061388 | TCCCAGCACTTGGGA[-/GGCC]GGCCGAGGTGGGCAG | 64326 |
rs573908372 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176107357 | GTTTCTTGGATACAA[C/G]ACTATTCCAGGACTG | 64326 |
rs573933768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176062233 | GGTCTCGATCTCCTG[A/G]CCTTGTGATCTGCCC | 64326 |
rs573939410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176131700 | TAAAGAAAAATCAAA[C/T]ATGAATAGTATTATA | 64326 |
rs573945108 | in-del | -/TAAAGGTT | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176047528 | TCAAAGTGTAAAGGC[-/TAAAGGTT]TAAAGGTTTAAAATC | 64326 |
rs573950480 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175973609 | TTGAAAAATATAATG[C/G]TTGCCTTGTAAAGCA | 64326 |
rs573956466 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176192013 | GTTCGAAAAGGATGA[C/G]ACCACAATGGAGTAG | 64326 |
rs574004447 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176139444 | GAACTACTATTTGAC[C/T]GAGTAATTCCATTAT | 64326 |
rs574016519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175982746 | TTACATGAACTTGGA[A/G]GACATTATGCTAAGT | 64326 |
rs574021289 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176127328 | AACTATAACTTTGTA[A/C]TCACTGACCAACTTC | 64326 |
rs574038914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176002509 | ATCCCTTCCCCTTCC[C/T]CCCCACCCCACAACA | 64326 |
rs574044854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176098372 | AATAAAAGATTATAA[A/G]AAGGTGTGGAAATGT | 64326 |
rs574068065 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176121331 | ACCTCCAGAGATATT[A/G]GAAATCATTCTTCAT | 64326 |
rs574068814 | in-del | -/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176097868 | AGTGAAACTCCATCT[-/C]AAAAAAAAAAAAAAA | 64326 |
rs574073211 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176152649 | AACTGGGTTTCACCA[C/T]GTTGGCCAGGCTGGT | 64326 |
rs574081244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176191083 | ACCTGATTCTTTGTG[A/G]TTTTATAATTTATAA | 64326 |
rs574087175 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176020270 | GAGCCAAGATCACGC[A/C]ATTGCCCTCCAGCCT | 64326 |
rs574098391 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176196316 | ATCAATAATATGAAA[A/G]TTGATCATTTGAAAA | 64326 |
rs574105199 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176110996 | GTCTCTACTAAAAAT[A/C]CAAAAATTAGCTGGG | 64326 |
rs574109671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176153265 | AGTTTACCTTATACA[C/T]GTCCCTGGGGTATAA | 64326 |
rs574116796 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176101609 | CCAGCAAAGGGTAAA[A/C]GTTTGTTTTACTAGT | 64326 |
rs574128950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176139393 | GCCACTGTGGAGACC[A/G]GAGTTGGGAGATTTC | 64326 |
rs574138660 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175968071 | CAGGATTTCACTATG[C/T]TGGTGCCAGGCTGGT | 64326 |
rs574160321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175977403 | TAAATGGCTTCTTTA[C/T]AGCAATTATAACAGA | 64326 |
rs574174741 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176202751 | TGCTAAAATGTAATT[A/C]ATAGGTAATGGCTAT | 64326 |
rs574181488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176030372 | TAGGCCCAAAGGTAA[C/T]TCACAATAGATAAGT | 64326 |
rs574212839 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176097831 | TCGAGATCATGCCAC[G/T]GCACTCCAGCCTGGG | 64326 |
rs574220944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176041842 | GGTGAAGCCAGGTGC[A/G]GTGGCTCACATCTGT | 64326 |
rs574249367 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant, downstream-variant-500B | RFWD2 | GRCh38.p7 | 1:175967407 | ATGAGAATTGCTTGA[A/T]CCCAGGAGGCAGGGG | 64326 |
rs574251094 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176000971 | TCCATCTCCTTTCCT[C/T]CCCAACCTTTGAAAC | 64326 |
rs574265048 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176138381 | AGAAAACCAGGGGAA[A/G]TGACAGTACCATTGG | 64326 |
rs574290264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176146314 | AACAAACGCTGTTAA[C/T]AGGCAAGTTCTAAGA | 64326 |
rs574294802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176179700 | CATGTTTGCACCACT[A/G]CACTCCAGCCTGGTG | 64326 |
rs574296422 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175991078 | TGCTTCTTCATTGGA[G/T]CATTTCAGATTTTGG | 64326 |
rs574301977 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176090238 | CTGCTGTCCTGCCTT[G/T]CCAGATCGAATCAAT | 64326 |
rs574322413 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176009274 | GACAGGTATTTTCCC[A/C]TGGAGATTTTGAGTT | 64326 |
rs574352546 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175970665 | TTGTACTTTTTCCTA[G/T]AATTTTCTTAAGGAT | 64326 |
rs574358587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176048886 | ATGCTGTCAAAAGAA[C/T]TAAGGGCCGGGCGCG | 64326 |
rs574359349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175971767 | TAATGTTCCAATTAA[C/T]AATGAGCACTACCAG | 64326 |
rs574411106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176164088 | TGCTACTACTACAAC[C/T]ACTATTACTATAGGA | 64326 |
rs574415491 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176075313 | AAAGATCTCCTCCAA[C/T]AGTTTCTTTAGCTAA | 64326 |
rs574439527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176095604 | AGAGGATGGCTTGAG[C/T]CCAGGAGGTAGTTGC | 64326 |
rs574465271 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176107778 | ACTGAGACAAATAGA[A/T]ACCATATGCCTCCAG | 64326 |
rs574465505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176066559 | TCCCTCTCAATCCTA[C/T]AAAATGTTTGTGTTA | 64326 |
rs574469698 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176045759 | TCCTTCAGTGAAAAG[C/T]AGAATATTCTTGTAA | 64326 |
rs574473018 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176149429 | TGAAAGTAACATAGC[A/T]TATAGACACTAAAAT | 64326 |
rs574475801 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176108396 | GAATTTTTGCACATA[C/T]GATTAATACCAGTAT | 64326 |
rs574498584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176135426 | TGAATAGTGAACTAG[C/T]ATATCATTAATTCAG | 64326 |
rs574500432 | in-del | -/CAAA | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176033943 | ATTTTATATGATCGC[-/CAAA]CAGACAAGAGTAATA | 64326 |
rs574511612 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176150217 | ATGCCTCTTGCAGAT[A/C]TTTGGATTTTAAAAA | 64326 |
rs574514008 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176017448 | TTTTTCTTAGGCGGG[A/T]AATAAATTTTGACCA | 64326 |
rs574539882 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175955623 | CTAGAATAAATAAAT[A/T]GTCTTCAGCAAGATT | 64326 |
rs574557182 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176038622 | CAAGAGTTCGAGACC[A/C]GCCTGACCAATATGG | 64326 |
rs574559405 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175965486 | AATCATTCTTTTATT[G/T]AAAGCACTTTCTAGT | 64326 |
rs574560836 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175993534 | CTAGAATAACCAATA[A/C/T]AGAGAAGTGCTTAAA | 64326 |
rs574572792 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176051087 | AAGGTAGCCTCACCG[A/G]TTTTATAATTAGTAG | 64326 |
rs574579069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176024185 | AATCACTTGAGTCGG[A/G]GAGGCAGAGGTTGCA | 64326 |
rs574585135 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176156558 | ACTGTTAAGGACACA[A/C]ACTTTATAAGGACAA | 64326 |
rs574619373 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176181149 | AAGTGGGAATAAATA[A/C]AGTGAAAGAAGTTCC | 64326 |
rs574628958 | snp | C/G | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176005361 | TTTCCTTCAGTTCTG[C/G]TCTGATTTTAGTTAT | 64326 |
rs574638772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176182375 | ATCAAGAACTTGTTC[C/T]TTTAGCGCTAGATGA | 64326 |
rs574667061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176045887 | TAATCCTCATTCAGT[A/G]CTCCATAGAGTCTCC | 64326 |
rs574688889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176072719 | CCCTCAATCTGGATC[C/T]ACATTTGCTGCAATT | 64326 |
rs574690435 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176128982 | ATCCCTGTCCTCCAT[A/C]TCCCTCCCAAGCATA | 64326 |
rs574690726 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176134806 | GAATTCATAACATTA[A/T]AGTATTCTACTCGCT | 64326 |
rs574697120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175984118 | TGTTAATCCCCAAGA[C/T]CACGGGGAAAATGTC | 64326 |
rs574703076 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176171562 | CTTTTCCTTTGCATT[C/G]ACACCTTGGCTAAAA | 64326 |
rs574707185 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176202322 | AGCTTCTTGAGTAGC[G/T]GGGACTACAGGCACA | 64326 |
rs574716547 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176012701 | TATATTGTATTCTTA[C/T]TGTAGCTTTTCTACA | 64326 |
rs574724678 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176087288 | TAAAGAGCTTCTGCA[A/C]AGCAAAAGAAACTAT | 64326 |
rs574725358 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176073339 | TTGATACAACTCCAT[G/T]CCAACAGTTTGAACA | 64326 |
rs574728424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176093876 | AAACAAAAACAAGTT[A/G]GCTGGGCATGGTGGC | 64326 |
rs574728487 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175963164 | TACAATGCACTATAC[C/G]CACTGCTATGATAAT | 64326 |
rs574752110 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175956656 | CAGGAGTGCAAAATA[C/T]AGTCATGCACTGCAC | 64326 |
rs574761439 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | RFWD2 | GRCh38.p7 | 1:176086231 | TGGGAATCTTTCTTT[C/T]TTTTTTTTTTTTGAG | 64326 |
rs574766374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176078443 | ATAACTAGCTAGCCA[C/T]GTGCAGAAGAATAAA | 64326 |
rs574770392 | snp | A/C | | | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175970489 | AATCTTGAATGTAAT[A/C]GTTTAGATACGATAG | 64326 |
rs574803903 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176021907 | ATTTCTCTAGCTGAC[A/G]GATTCCATCTTCTAT | 64326 |
rs574819293 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176008251 | CACTGTCTGGCACTT[C/G]CTAGTGAGATGAACC | 64326 |
rs574823674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176037097 | ACTGACAAATTCTAC[C/T]AAACATTTAAGAACA | 64326 |
rs574825830 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175963635 | TTGGTACTTAATAGA[A/T]GTGTTTGTTTATGGT | 64326 |
rs574834782 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175972718 | TGATCTGCCCGCCTC[A/G]ACCTCCCAAAATGCT | 64326 |
rs574842376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176187352 | TATACACACATATAT[A/G]TACACATATATACAC | 64326 |
rs574861788 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176051292 | AAAAACCAAGATGTT[-/A]AAAAAAAACACATTA | 64326 |
rs574863976 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176201530 | CTCATTATCAGAAAA[-/G]GTATAAAGATTTGTA | 64326 |
rs574865740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176188017 | TCCCCTCTTCCCTCC[A/G]TGAGATCAGGCAGAT | 64326 |
rs574874646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176048609 | TATCTGGTAAAGGAC[A/G]GAGTTATTATCAGAA | 64326 |
rs574879651 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176078295 | CTGGTAGGTACAAAA[A/G]CAGACATAAGACCAA | 64326 |
rs574886573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176172249 | GTCTCGCTATATTGC[A/G]CAGACTGGTCGCAAA | 64326 |
rs574905613 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176138128 | AATTCTGCCAAGTGG[-/A]AAAACAGTGAGGCAT | 64326 |
rs574906121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175999723 | CCAATTTACATTCCC[A/G]CCACCACTGTACAAG | 64326 |
rs574925676 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:176093015 | ACGTCAGTGACAACT[A/C]CAGCCACAGGCATCA | 64326 |
rs574927185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175990401 | CTTATTTTTAGTCTT[A/G]AATATGGTGTCCCCT | 64326 |
rs574929450 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176208276 | CCAGCCTGGGCAAGA[C/T]AGCGAAACCCCGTCT | 64326 |
rs574947212 | snp | A/C/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176099963 | CTTGTGGAAGAGTTC[A/C/T]GTCCAAGCCAATCTA | 64326 |
rs574955703 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176208846 | CACTTTGGGAGGCCA[A/G]GGCGAGTGGATCACC | 64326 |
rs574970869 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176003972 | AGGATATTGATTCTT[C/T]CAACCCATGAGCATG | 64326 |
rs574975904 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175974568 | ATAACAATGATTAAT[A/C]TGGTTAAAGGGGTTG | 64326 |
rs574978804 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176024754 | TAGAGATACAAGAGA[G/T]ATATATAAAAATCAA | 64326 |
rs574980763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176113424 | ACTGTTTGAGTCCAT[C/T]ATATATTCTGGTTAT | 64326 |
rs574982565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175990990 | ATATAATTATTAATA[A/G]GTTGCACATCTGAAA | 64326 |
rs575006071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176086656 | TCATGGATAGGAAGA[A/G]TCAATATTGTGAAAA | 64326 |
rs575011228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176065832 | CCTGCCTGAGCCTCC[C/T]GAGTAGCTGGGATTA | 64326 |
rs575011947 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176080143 | AACACGCTGTATGCA[A/C]TAAACACAATTTTAT | 64326 |
rs575019525 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176099634 | TAAGAATCCATTTTC[C/T]TTTGCAACTGGATGC | 64326 |
rs575033521 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176030130 | CTAATATATTTTTTT[A/T]AAAGTAGAGATGGAG | 64326 |
rs575051235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176030790 | TAATTGTGTTCCCCA[A/G]AAAGACATGTTTCAG | 64326 |
rs575056064 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175948528 | AACTCTTGGCTTGTA[C/T]GTTAGAAAAGTTACT | 64326 |
rs575056279 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176086265 | GAGTCTCACTCTGTC[A/G]CCCAGGCTGGAGTGC | 64326 |
rs575061542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175994185 | AATACTTTACAGACA[A/G]ACAAATGCTGAGAGA | 64326 |
rs575089682 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176069824 | AATCCCATCTGTAAG[A/T]TCTCATGATCTAATC | 64326 |
rs575091267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176121253 | TTTAATATTTAATTT[C/T]AAATTAATAGTAAAT | 64326 |
rs575102771 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175981503 | GTTGAGTATCTCACA[A/C]CATATACAACACTCA | 64326 |
rs575103480 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176130220 | AATAAAGTCTGAGCT[A/G]AAAAGTTAAAAAATG | 64326 |
rs575110898 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176199089 | TTGGGAGGCCGAGGC[A/G]TGGGGACCATGAGGT | 64326 |
rs575123235 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | RFWD2 | GRCh38.p7 | 1:176155963 | AATCAGCCAGATGGA[G/T]GCGAGAAAAAATGAA | 64326 |
rs575146207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992455 | AGGCATTGCCTCACT[C/T]GGGAAGCGCAAGGGG | 64326 |
rs575147348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176172791 | AACACATGGATCGAC[A/G]TATCTCAATGACATT | 64326 |
rs575165230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176179032 | GCAGCGGCTCACGCC[A/G]TAATCCCAGCACTTT | 64326 |
rs575166425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176126604 | TGGGAATGCAGGTAC[A/G]CGCCACCATGCCCAG | 64326 |
rs575180933 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175944920 | AGATAACACCACCAA[C/G]AGCAGCAATGTCCAT | 64326 |
rs575184158 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176173354 | AAAAAACCAGTAATT[C/G]GCCAGGCACAATGGC | 64326 |
rs575184630 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176166819 | GTACATGCCTGAATT[C/G]CCCGCTACTCAGGAG | 64326 |
rs575199219 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175960251 | CTTTGGAGTCTGAAA[C/G/T]ATTTCAATTCAAAGC | 64326 |
rs575214647 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:175965755 | ACCAAACCCAGCTAA[-/T]TTTTTGTATTTGGAG | 64326 |
rs575221568 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176186744 | TAGAAATGGTTACGG[A/G]AGCTATCATAATCCA | 64326 |
rs575234381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176137264 | AATAACACTTAATAT[A/G]TTGAACCATTCCCTT | 64326 |
rs575236536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176131017 | TGGGGTCTTTGGGGA[C/T]AGTTACTTAACAGCT | 64326 |
rs575264211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175995816 | CGAATTCTACCAGAG[A/G]TACAAGGAGGAACTG | 64326 |
rs575265756 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176069518 | TCCTCAGGTATATCA[A/G]GTAAACAGGAATACC | 64326 |
rs575270392 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176002405 | ACATGTGCACATAGT[C/G]CAGGTTAGTTACATA | 64326 |
rs575271127 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:175990762 | CTACTCTAAGTATAT[A/T]CTGTTCGACCTAAAT | 64326 |
rs575284602 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176006795 | CATTTTTTCCTTCAT[A/T]TCAACTTTGGTGAAT | 64326 |
rs575296019 | snp | A/C | 0.030665 | 0.119967 | intron-variant | RFWD2 | GRCh38.p7 | 1:176205963 | ACTACAGTCGTCTCA[A/C]CAGCCGATTCCTAAG | 64326 |
rs575302896 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176174927 | CTTAGGGTAGTTAAC[A/G]TGCAGAATTTTTCTG | 64326 |
rs575309498 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176040654 | ATTCCATTCTGTATA[C/T]AGTAGGAATAAACAA | 64326 |
rs575310966 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175959563 | AAAAATCCAAGGAAC[A/G]TAGAAATGAATAATT | 64326 |
rs575311699 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176129249 | CCCTACACTTTGATT[A/C/T]GTCTGGAACTTTGTC | 64326 |
rs575321615 | in-del | -/A | 0.00597247 | 0.0543191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176171708 | AAATGCAACTTCTAT[-/A]AAGTGCAATAAAGCA | 64326 |
rs575327714 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175996204 | ATTCAACAACCCTTT[C/G]TGCTAAAAACTCTCA | 64326 |
rs575345004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176076802 | CGTTACAACCAATAC[C/T]ACAGAAATACAAAAG | 64326 |
rs575354063 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176019043 | GGTGGTACACACCTG[-/T]TGGTCCCAGCTACTT | 64326 |
rs575354247 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176111051 | CAGCTACTTGGGAGG[C/T]TGAGGCAGGAGAATC | 64326 |
rs575354354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175988173 | TCATGTCTATTATAC[C/T]ATCTTCTGAGTGCAC | 64326 |
rs575369667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176097051 | TTACTTTCTTTGAGC[C/T]TTTAGTAAAGTTTGA | 64326 |
rs575380846 | in-del | -/A | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176177350 | TGAGAAAAAAATATT[-/A]AAAAAAAAAAAGAAA | 64326 |
rs575391403 | snp | A/G | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176186386 | AAACTAGCAAGCATA[A/G]GGGCACACACCTGCA | 64326 |
rs575396453 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176144561 | AGTTTACCATGGAAA[C/T]GTACTAGCTGATTCT | 64326 |
rs575399607 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176117176 | AGGCTAGCTATTTAT[-/A]ATATCATCTAGAGTC | 64326 |
rs575432987 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176018165 | TATTTACCCTTTACT[C/T]TGTGAATAATCTCTC | 64326 |
rs575438931 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176046967 | AAATAAATAAATAAA[A/T]AATCTCCTTTCCTTC | 64326 |
rs575443730 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176043109 | TTGAGTAAATATTTG[C/T]ATTTCTGCCGATGAA | 64326 |
rs575453129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176035140 | GATGTTGGATCCCAA[A/G]ACATTAAATGAAACA | 64326 |
rs575458003 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176002040 | GATTCTCTTCCCGCC[G/T]TTCAAGAGTTTCAAT | 64326 |
rs575458169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176097609 | TGCAGCAGCTCAAGC[C/T]TGTAATCCTAGCACT | 64326 |
rs575477828 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176117187 | TTTATATATCATCTA[A/G]AGTCCCTCCCAGCTT | 64326 |
rs575482434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176144972 | AAGACTTCTTTAAGT[A/G]ACACAAAACACACTA | 64326 |
rs575505675 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176024469 | CTCTTAGCAAACTAG[A/G]AACAGATAAAAAATT | 64326 |
rs575505781 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175994837 | ATTAGACAGATCAAT[A/G]AGACAGAAAGTCAAC | 64326 |
rs575523940 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992645 | AGTCTCGCTGACTGC[A/G]AGCACAGCAGTCTGA | 64326 |
rs575525589 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176165383 | GTGTGTGTGTGTGTG[G/T]GTGTGTGTGTGTGTG | 64326 |
rs575531574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176018920 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGCCGAGG | 64326 |
rs575540266 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175993413 | GGCTTTGACGAGTTG[A/T]GAGAAGAAGGTTTCA | 64326 |
rs575544869 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176020325 | CGGAAAAAAAAAAAA[A/C]AAAAAACCTTCATAC | 64326 |
rs575553397 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176115612 | AAATTAGCTGGGCGT[C/G]GTGGCGCGTGCCTGT | 64326 |
rs575556258 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176151197 | CAATTCTCCCATTTT[C/T]GGATAAGGAAGCGTG | 64326 |
rs575562819 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176115175 | AAAACGTGGCCGGGA[A/G]TGGTGGCTCACGCCT | 64326 |
rs575568245 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176020740 | GTAGGAAAATATGTA[C/T]CAAATAATTTAAAAT | 64326 |
rs575588013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176124474 | TATTCTCTATCTTCA[C/T]GAGTTCAATTGATTT | 64326 |
rs575597660 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175986014 | TTATATAAATCAAGA[G/T]AGTAACAAGAATTAT | 64326 |
rs575641965 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175995505 | AGACCACTAGCAAGA[C/T]TAATAAAGAAGAAAA | 64326 |
rs575650685 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176039755 | AAGACTAAAGATAAA[C/G]TCTTGCATATATGGT | 64326 |
rs575680321 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176182933 | CCTAATCATTCCTTT[C/T]CCTCTGATAACCTCT | 64326 |
rs575685474 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176107684 | ATACAATGATAGATG[C/G]TCAAAGGGAAGAAAC | 64326 |
rs575704067 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176067453 | GCAGAGGAACACATC[A/G]GTACAAGAGCACACT | 64326 |
rs575706790 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176054282 | TTCTCCTGCCTCAGC[C/T]TCCCAAGTAGCTGGG | 64326 |
rs575724125 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176204305 | AACGTGAAGCATAAG[A/C]ATATCTTTAAAATGT | 64326 |
rs575728828 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176119266 | AATCCCTTAGTGTTT[C/G]TATAACACTAATAAA | 64326 |
rs575742587 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176067881 | TGCTGTGGGGTCAGA[C/G]CCCACGCTCCCACGA | 64326 |
rs575749180 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176022148 | ATATTGGGACTTGTA[A/G]AGTCTTTTATATGTA | 64326 |
rs575758591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176170907 | GAGACTGGTGGATCA[C/T]GAGGTCAGGAGATCA | 64326 |
rs575770575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175949987 | AAATTAGCCCCAATA[C/T]AAATAAGATAATCTA | 64326 |
rs575815646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176074290 | AGGAATTAGAAGGCG[C/T]TGAAGTAAATTTATT | 64326 |
rs575827907 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176103601 | AGCATTTCTTTTGAG[C/T]ACCATATCACAGCTC | 64326 |
rs575839080 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176054706 | AAATTTCCCTCCTCT[C/G]TCCTGTATCAATCAA | 64326 |
rs575853075 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176182500 | TGGTACTGGGTAGGG[C/G]TCAAGTATACTGCTA | 64326 |
rs575859321 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176010737 | AATGATGCTATCTCC[A/G]CAGCCATTAAGAAGA | 64326 |
rs575867276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176060789 | ATATTTAAAAATGTG[C/T]CCCCAAAATATCAGT | 64326 |
rs575872043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176205006 | CACTGAACTTCATAT[A/G]GTGCCTGGCCGACAG | 64326 |
rs575881164 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176141857 | CACCTCAGCCTCCCA[A/C]GTAGCGGGGACTACA | 64326 |
rs575884593 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175972855 | TTAATTTTTTGAGAC[A/G]GAGTTTCGCTCTTGT | 64326 |
rs575894573 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176159047 | AAAAGACAAAAAATT[A/C]TAAGTGATGAACCAA | 64326 |
rs575903707 | in-del | -/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176151953 | CCATTTTGAGGGCAT[-/T]TTTTTTTTTTTTTTT | 64326 |
rs575926565 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176103642 | AAATCTTGGAACATT[A/G]CAAATTCTGGATTTT | 64326 |
rs575933237 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176008308 | TCACCCATCTTCTGC[A/G]TTGCTCATGCTGGGA | 64326 |
rs575937778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175989571 | TTTTTCATTAAAAGT[C/T]TCACATATGATGTCT | 64326 |
rs575941879 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176016338 | GTGAAAAAAAACCAG[A/C]GGGTGTTGTTTTAGA | 64326 |
rs575949318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175973459 | AATTAATTCAGAAAA[C/T]GTTGAATTTTACTGC | 64326 |
rs575954678 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207695 | GAAGGAGCTGTCTCT[C/G]TCTTCTGAGGGGTAG | 64326 |
rs575970962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176162474 | ACCAATGGACACCTG[C/T]TGAAAGAACTGTATG | 64326 |
rs575981833 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176022778 | AACCTCAATGTGCCC[G/T]CAGCATCCATTTCCA | 64326 |
rs575986268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176197223 | AGTGGCCCAACCTAG[A/G]CAAGATGGCAAGACC | 64326 |
rs575998978 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176158201 | TTAAGAAGACAAAAG[A/G]TAAGAATGACAGCAG | 64326 |
rs576000021 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RFWD2 | GRCh38.p7 | 1:176187313 | ATATACATACACACA[C/T]ATATACACACACATA | 64326 |
rs576004346 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175974624 | ATCGAATAGGTAATT[G/T]CAGTGAAGAGATTAT | 64326 |
rs576011123 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176201261 | ATAGAGGATACTCAC[C/T]CTGTAATACAAATTT | 64326 |
rs576029723 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176068535 | TTACAACATGCCATA[A/T]AAAACACAGAAAAAT | 64326 |
rs576031940 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176008529 | TTTTCCTTTAACTCT[C/T]TGTGGTTTAATTACC | 64326 |
rs576035238 | in-del | -/CCCGGCTGCCA | 0.0123036 | 0.0774623 | intron-variant | RFWD2 | GRCh38.p7 | 1:176057745 | AGATTGCAGCCTCTG[-/CCCGGCTGCCA]CCCCATCTGGGAAGT | 64326 |
rs576041578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176029394 | GAAGCAGAAAATGAG[C/T]TGCCATTTTACAAAG | 64326 |
rs576046333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176197953 | AAATTTTAAAAATAT[A/G]GTGAAAAACCTCAAC | 64326 |
rs576048665 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176098417 | GGTCTAAGGATTGTT[A/C]TGAATTAGATAAGAT | 64326 |
rs576054082 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176171876 | ACAAAAAAAGGTAAT[C/G]AATGAAATTTCTGGT | 64326 |
rs576055348 | snp | C/G | 0.00358779 | 0.0422022 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207377 | CTCGGGGTCGGGGCT[C/G]CCTGGCGAAGGGAGT | 64326 |
rs576057953 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176077827 | TACAAAATCGATGTA[C/T]AAAACTTGGTAGCAT | 64326 |
rs576070503 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175978381 | TTATAATATTCACCA[C/T]AAAGTATCTAATGCA | 64326 |
rs576073632 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176029950 | TAGGAATCATTATTA[G/T]TAGTAGTAGTATTTT | 64326 |
rs576092030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175974152 | GCAGGACATAAACTA[A/G]ACTAAATGGCAGGAG | 64326 |
rs576096115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175982047 | TGGCAAGAATGTGGA[A/G]AAAAGAGAACTCTTG | 64326 |
rs576107368 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176072246 | AACAAGCAAATATGT[A/G]GACATATATGGACAA | 64326 |
rs576113018 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175988919 | TAAAAGCCAACCAAG[A/T]AATATTTAAAACCAA | 64326 |
rs576114384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176057908 | CGTCTCTGCCCGGCC[A/G]CCCATCCTCTGAGAT | 64326 |
rs576147440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176063306 | ACCTCATGATCCACC[C/T]GCCTCGGCCTCCCAA | 64326 |
rs576150018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176004597 | AGGCTTTTTCTGCAT[C/T]TATTGAGATAATCAT | 64326 |
rs576150307 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176184299 | CGTTCTCCAACCTAT[C/T]CCCACAAGTGAGTAA | 64326 |
rs576162433 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176174746 | TCTAATACAAAAGTA[C/G]TCACCACACCCTAAC | 64326 |
rs576168542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176200140 | TACAAAATGGGAACT[A/G]TAAGAGTATCTACAG | 64326 |
rs576173719 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176105198 | AGCTGAAAGGGTAGC[C/T]GTTATTGATTATAAC | 64326 |
rs576177259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176100934 | CCTAGGAAAGAAAAC[C/T]GGATCTGATGGATCC | 64326 |
rs576186596 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176196731 | TAGAAGGGGAACATT[C/T]CATATCGTCTTTTAG | 64326 |
rs576191035 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175946500 | ATCAGCAGAGAATAT[G/T]TGGAAAAAACAGGTA | 64326 |
rs576203845 | snp | C/T | | | missense, intron-variant | RFWD2 | GRCh38.p7 | 1:176135077 | CAGGAGAGTATAAGC[C/T]ACTCATTTCCTGAAA | 64326 |
rs576233990 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176202134 | ACATACATTGCTGCA[C/G]AAACTGTTACTGTCT | 64326 |
rs576243927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175993447 | GATCAAACTACTCTG[A/G]GCTACAGGAGGAAAC | 64326 |
rs576247106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176057041 | TCCTTATGCAAATGA[A/G]AATCCTATAATTAAC | 64326 |
rs576272685 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176173941 | GCAGTGAGCCGAGAT[C/T]GTGCCACTGCACTCT | 64326 |
rs576280968 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175968788 | TCATCATTCCTTTCT[C/T]AATGCTTTCCAAAGT | 64326 |
rs576284465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175969706 | CTTACAGAGGTCTCC[A/G]TCATGAATCAAGCCA | 64326 |
rs576285023 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176091011 | AAAGAAAGATAATTT[A/C]TTTAGGAACAACAAT | 64326 |
rs576286091 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175977173 | TTTATCAGAGAGCAA[A/C]AGATCCTGAAGATAA | 64326 |
rs576342610 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175970377 | GCCGGAATGGGAATA[G/T]TATGGGACAATGAAG | 64326 |
rs576345096 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176056063 | TGATTTCCATTTTGA[A/T]CCCAGCGTTGCCAAA | 64326 |
rs576352355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176196025 | AATAAATTAAACAAC[A/G]TACTTCTGAATAATC | 64326 |
rs576352984 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176107645 | TGGACAACTAACACA[C/T]TAACAATTATTATTA | 64326 |
rs576359508 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176007628 | TCAGTGTGCCCCTGC[G/T]GGGGGGTGTCTCCCA | 64326 |
rs576362853 | in-del | -/TT | 0.00279162 | 0.0372561 | intron-variant | RFWD2 | GRCh38.p7 | 1:176002184 | TTTTCTACCTCTTTC[-/TT]TCTCTCCTCATCTTT | 64326 |
rs576367295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175976387 | GGTTCAAGTGATTCT[C/T]CTGCCTCAGCCTCTT | 64326 |
rs576367908 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175997643 | GCCAAAAAACACATG[A/G]AAAAATGCTCATCAT | 64326 |
rs576402992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176056872 | AAACACTTTATTAAT[C/T]ACTACAGAAAGAAAT | 64326 |
rs576410677 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176095852 | TATTCATAATTTTTT[A/T]TAAAAAAACATATAA | 64326 |
rs576441168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176190651 | GCAATCCGGCCCAAG[C/T]AACATCGTTAATCAG | 64326 |
rs576452134 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176104649 | AAAACTATGAAACTT[C/T]TCAAAGTCATTCTGT | 64326 |
rs576465674 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176146501 | CAATATCCTCTCTTG[C/T]TTTCTTACTTGTTCC | 64326 |
rs576473350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175965628 | GAGTCTCGCTCTGTC[A/G]CTCAGGCTGGACTGC | 64326 |
rs576474950 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176111514 | TGGCCAGGATGGTTT[C/T]GATCTCTTGACCTTG | 64326 |
rs576503742 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176153343 | GAAAAGTGGATGACT[C/G]TAAAGACTAGATAAC | 64326 |
rs576511592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176105451 | GGAATTTCAAAGAAA[C/T]ATCTCTAGTTACATT | 64326 |
rs576531899 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175955247 | ACCCTGCCTCAAAAC[-/A]AAAAAAAAGAAAAAG | 64326 |
rs576538894 | snp | A/C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176157819 | TAAGGGAAAAAGTCA[A/C/G]TCTATATGGAGCAAA | 64326 |
rs576551489 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176049409 | GTTTTTAATATATTA[A/C]GGTATCAAGAACCTG | 64326 |
rs576552856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176059939 | AAAGTCAAGCAATGA[A/G]TTGAAATTTGACTCG | 64326 |
rs576554143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176180995 | GGCTTGGTAGACATA[C/T]GGTACAGGGCACAAG | 64326 |
rs576577515 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176189789 | AAGCAAGCCAGAAAA[A/C]TATGACCAAAACAAA | 64326 |
rs576610064 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176012909 | TTTCTCAGAATGCAT[A/C]CCCATCCTTGAGCAA | 64326 |
rs576612922 | in-del | -/GTAT | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176132499 | CAAACCAAGATGGGG[-/GTAT]GTATGTGTGTGTGTA | 64326 |
rs576618939 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176166697 | ATCCCATTATTTAGG[A/G]AGGCTGAGGCAGGCA | 64326 |
rs576619553 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176013725 | TACAAAAGGACCTTT[C/T]ATAGCTGGTATACTT | 64326 |
rs576629255 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175961321 | ATTGATTCACAGAGA[A/G]AATAACTTTCAATCA | 64326 |
rs576634329 | in-del | -/ATA | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:176156712 | AAACATATCCATTTC[-/ATA]ATAATAATAATAAAG | 64326 |
rs576638141 | in-del | -/TA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176021049 | ACAATCACAGCTCAC[-/TA]TATAACCTTGAACTC | 64326 |
rs576645423 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176050058 | TTATAAAAATTTACT[G/T]CATGACAAATTCAAT | 64326 |
rs576648065 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175999977 | TTTTTCCCTACAAAA[C/T]TGTCTGAGCTCCTTA | 64326 |
rs576650913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992072 | TGTGCTAGACTTTTT[A/G]AACATTTTTAATTTT | 64326 |
rs576652236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176007983 | TCAGACTGCTCTGCT[A/G]GCAATCAGGGAGACT | 64326 |
rs576660480 | snp | C/G | 0.0991586 | 0.199366 | intron-variant | RFWD2 | GRCh38.p7 | 1:176003030 | CCTGTTGTTTCCTGA[C/G]TTTTTAATGATTGCC | 64326 |
rs576675960 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:175962293 | CTGTACCCCAGTTAC[A/T]TCCTGTACCAGGAAA | 64326 |
rs576681503 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175965904 | TGGGTTTGATTCATC[A/G]TAAGAATCCCCTTAT | 64326 |
rs576682019 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176141522 | TACATACATACATAC[A/G]TACAGCAGCAAAACT | 64326 |
rs576689159 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175963851 | TTGGGTTCATACTAT[A/C]GTTATTTATGAATAT | 64326 |
rs576693745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176096427 | TGCATGGCCATGTCT[A/G]CCACATGAGTGCAGT | 64326 |
rs576699586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176183560 | AGTTTCTCAAAAAAT[C/T]ACAAACAAAATTACC | 64326 |
rs576702923 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176174185 | CACCAAAATCTTCAG[A/T]ACATCACATTCCTTT | 64326 |
rs576724711 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176053442 | CTAACTTTCAGCTCA[A/C]TGTCATTTTCTTAAA | 64326 |
rs576726887 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176005969 | AATCTCCCATTATTA[A/T]TGTGTGGGAGTCTAA | 64326 |
rs576730483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176088378 | AGGATTAAAAACAGG[C/T]GAATTATGAGTTTCT | 64326 |
rs576746029 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176182192 | AAAAACCTCACTTCA[C/T]AATCTATTTCGTATT | 64326 |
rs576753888 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176036512 | AACAAAAAAACAAAA[A/C]AAAAAAAAAAAAAAG | 64326 |
rs576754234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176102887 | CAGTGCAAGAGGACA[A/G]CTTCAATTCCCCATG | 64326 |
rs576764019 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176114163 | ACTGCTATTCTCTCT[C/T]AAGTTCCTACGGTAT | 64326 |
rs576765187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176045967 | TTTAATTTGGCAACC[A/G]GAAAAAAAAAAAAGG | 64326 |
rs576776536 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176041910 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 64326 |
rs576778871 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176019604 | GGTGGCTCACACCTG[C/T]AATCCCAGGACCATG | 64326 |
rs576794270 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176140409 | ATCAGGCAAGAAATA[A/T]TAAAAAGAAAAAAGT | 64326 |
rs576798787 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176180056 | TCTACTACTTCACTA[C/T]CACCCCAAAAGAGAC | 64326 |
rs576812694 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176113091 | GTTGTTGGAACATAT[C/G]ACAGTTCTATTTTTA | 64326 |
rs576822594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175953787 | AAAAAAAACTCCTAT[A/G]TACATATATATCTAA | 64326 |
rs576826524 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176112375 | CGTGCAGGTTTGTTA[C/T]GTATATATACATGTG | 64326 |
rs576853723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175948436 | GAAACAGATAAAGTG[A/G]TCTAATTTGAATGTA | 64326 |
rs576856498 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:175983652 | TTGGAACAGTTTAGA[A/G]GGTTCAGAAGACAGG | 64326 |
rs576860618 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176040536 | GCTGGTCTCAAACTT[C/T]TGACCTCAAGCCATC | 64326 |
rs576864683 | snp | C/T | | | intron-variant, utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175971467 | AATCCCAAAGGGAGT[C/T]TGTTGAAAATGGAGG | 64326 |
rs576895145 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176169043 | TGACAATAAATCAGT[-/A]AGTGCTTCTTTAGCA | 64326 |
rs576908139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176102310 | TCACCCTTGTACGTG[C/T]CTGCAAGCCTAATCT | 64326 |
rs576920243 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176197071 | CTCAGAATTTGCATT[G/T]GAAAATAAAGCCTTT | 64326 |
rs576939841 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant, utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175971785 | TGAGCACTACCAGAA[G/T]GTTCTAGCCTTTGCT | 64326 |
rs576950124 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176104275 | CTCTACATCCTGGTT[A/G]TAGGGAGAAGCTTTT | 64326 |
rs576952614 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176010960 | TGGTAGGAGCCTGAG[A/G]ACAGATTAAAGTACA | 64326 |
rs576954402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176081451 | TGGTCAGTTTTTCAG[C/T]TTTAATAAAAAATGT | 64326 |
rs576958795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176135479 | TAAGATAAATATGAC[A/G]GTAAGATAACTGGAT | 64326 |
rs577002600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176164587 | AACCATGCCTTCATA[A/G]GGGGATGATATCTGG | 64326 |
rs577017935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175958541 | TGATAAGCATTTCCA[C/T]CCTACATTTCTCCTC | 64326 |
rs577021009 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176066598 | CAGCCCAGTGGCTGC[G/T]GACTTTTACGTCAAG | 64326 |
rs577031544 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176143034 | AAAACAAACAAAACA[C/G]AGAGGAAAAACAAAG | 64326 |
rs577032831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176046800 | TGAATTACTGAAGCA[A/G]TTGGGTGATGACAAG | 64326 |
rs577040293 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175952751 | TTGTTGCTACTAAAA[A/C]TAAAAAAAAACATTA | 64326 |
rs577043177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176006317 | AATTTGCCAGTCTGT[A/G]TCTTTTCATTGGAGC | 64326 |
rs577060475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176059225 | ATTCATCTATCAAGT[A/G]TATTCTGTATGAAAC | 64326 |
rs577078847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176170357 | CTATGGCAGTTATTA[C/T]GAAATGTGTTTCTTC | 64326 |
rs577084145 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175959137 | TTGGGCTTATTCCAG[C/G]GAATGTAAAGTTGGT | 64326 |
rs577084313 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176078641 | AAAACAAAAATTGAC[A/C]AGTGGGACCTAATTA | 64326 |
rs577096396 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176177523 | AACAGTATTTGTTTC[A/T]GGGTCATATAATTAT | 64326 |
rs577105562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176001539 | GAGATATTTCGTGGC[A/G]AAGTTATCTCAGGGT | 64326 |
rs577110671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175949066 | TAGGCAGGAGGCTGA[A/G]GCAGGGGAAGTGCTT | 64326 |
rs577137499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176164152 | TTTCTCAATGATGAC[A/G]CTATTGGCACTTGCT | 64326 |
rs577137730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176170743 | CATCAACCCCTATCA[A/G]GAGAGTCAGCCTGTC | 64326 |
rs577147554 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176032793 | CTGGAACAAGGTAGG[G/T]GAAGGGGAACTACAC | 64326 |
rs577152686 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176079357 | GCTAGAGGCCATTAT[A/C]CTAAGTGAATTAATG | 64326 |
rs577160045 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176176234 | AACATCAAGGACACT[C/G]TATACAAATTTAACA | 64326 |
rs577175935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176127449 | CAAGATCATACAATA[C/T]CTGTCTTTCTGTGCC | 64326 |
rs577187754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176131594 | ACTTTTTAGTGAGGA[A/G]TAAGAACAAAAACTG | 64326 |
rs577191373 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175946997 | ATCCAGCATCCATAC[A/C]ACCTCAATAAGCACT | 64326 |
rs577195943 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176035176 | TAAAGCAACTATTGT[A/C]ATTATACTCCATGGG | 64326 |
rs577211108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176030924 | ATCCATTGACTGGTG[C/T]CTTCATAAGGAGAGA | 64326 |
rs577233261 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RFWD2 | GRCh38.p7 | 1:176181734 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 64326 |
rs577254904 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176133914 | GGCTTAAAGATAACA[A/C]TATACACAGACCAAG | 64326 |
rs577257080 | snp | A/G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175949664 | CTGCAAGAAAGCTAC[A/G/T]GCCAAGAGCCACCAC | 64326 |
rs577264169 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175944945 | GTCCATGGAGTTACA[C/T]TGATGGTGGAGAGTT | 64326 |
rs577281398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176041329 | AGAAATCAATTTCTC[C/T]ACTTGGATTTTTTTT | 64326 |
rs577301685 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176131098 | CTAACATTCTGCTTT[A/G]AGAGTTACATACAAT | 64326 |
rs577323679 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175978814 | AGAAAGAGAAGAAGC[G/T]TCTATGTTGTCTTCT | 64326 |
rs577324554 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175994521 | CGTGCAGAGACACAC[A/G]TAGGCTCAAAATAAA | 64326 |
rs577356711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175984615 | CCAGACCCCAAAATG[A/G]TAGATCCACTGACAG | 64326 |
rs577364338 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176156599 | AAAGTACAAGCATGA[A/T]GAAGACTATACCATG | 64326 |
rs577369469 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176093937 | CTCAGGCAGGAGAAC[C/T]ACTTTAACCCAGGAA | 64326 |
rs577396219 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176187039 | CTACTTATACTAAAA[C/G]TTACAGTACCTAAAA | 64326 |
rs577397475 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176161407 | TACTGTAGGCCAATA[C/T]AGTGAGACCTGTATC | 64326 |
rs577411358 | snp | C/G/T | 0.0023933 | 0.0345097 | intron-variant | RFWD2 | GRCh38.p7 | 1:176031708 | TAGTTGGCCATAAAT[C/G/T]TGTTACTTAACACTA | 64326 |
rs577422267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176031417 | TAATAAGAACACCTT[C/T]ACTGTTACTTTTTCC | 64326 |
rs577424420 | in-del | -/AAAAAAAAAA | 0.153665 | 0.230694 | intron-variant | RFWD2 | GRCh38.p7 | 1:175949168 | GCAAGGCTCCGTCTC[-/AAAAAAAAAA]AAAAAAAAAAAAAAA | 64326 |
rs577443601 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | RFWD2 | GRCh38.p7 | 1:176200930 | AGTTTCACTACATTG[A/C]CCAGGATGGACTCAA | 64326 |
rs577446537 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176056564 | AATGCTTTCTAGCCT[C/G]AATTAAACCTTACTT | 64326 |
rs577455331 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176063912 | TTAAGTAAGTAATGA[A/T]AAAACATAAAATAGC | 64326 |
rs577455952 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176209005 | AATCGCTTGAACCCA[A/G]AAAGCGGAGGTTGGA | 64326 |
rs577471847 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176167383 | ATCGTGGTCCCTGAC[A/G]CATAGTAGGCGCCTG | 64326 |
rs577477578 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176166168 | GTGTGACTCTGTCAC[A/G]CAGGATGGAGTGCAG | 64326 |
rs577485490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176024281 | AATGTATAAAACTAC[A/G]GATGAATATCCATTA | 64326 |
rs577488584 | in-del | -/C | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175954943 | AATATATATATATAA[-/C]TTCACTATGTAAAGA | 64326 |
rs577532666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176114798 | TCACCATGTTGCCCA[A/G]GCTATATTAGGGTAA | 64326 |
rs577536190 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176168204 | CTGGGATTACCGGTG[C/T]GCACCACCACACTTG | 64326 |
rs577536231 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176160466 | AGCAAAAGAAACTAT[C/T]ATCACAGTGAACAGG | 64326 |
rs577539597 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176124518 | ATAAGTGAAAACATG[C/T]GTTGTTTATCTTTCT | 64326 |
rs577543771 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176041766 | AGGTCAGGAGTTCGA[C/G]ACCAGCCTGGCCAGC | 64326 |
rs577558258 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176076244 | AAGTCTCAATAAATT[A/T]AAAAAAAATCATAAT | 64326 |
rs577562041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176173385 | TCACATCTGTAATCC[C/T]GACACTTTAAGAAGC | 64326 |
rs577578017 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176124849 | AACCTCCAAACCATT[C/T]TCCATAGTGGTTGTA | 64326 |
rs577596421 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176076920 | AAGATTCAAACAATA[A/C]GAAAGTGAAAATCTG | 64326 |
rs577606204 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176027460 | TTTAGAGCCTAATAA[C/T]AAAAACAACATTTAA | 64326 |
rs577607022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176121326 | CAGAGACCTCCAGAG[A/G]TATTAGAAATCATTC | 64326 |
rs577619792 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176135775 | AAAGATGCATAATCA[A/G]GTAAAATTATTTCTA | 64326 |
rs577621937 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176008104 | TGGGAGTGACCCGAT[C/T]TTCCAGGTGCGTCCG | 64326 |
rs577623335 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176059671 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 64326 |
rs577634409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176179163 | GGCATATTGGTGCAC[A/G]CCTATAGTCCTAGCT | 64326 |
rs577643761 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176002420 | GCAGGTTAGTTACAT[A/C]TGTATACATGTGCCA | 64326 |
rs577646009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176121947 | AGATGGAGACCATCC[C/T]GGCTAACACAGTGAA | 64326 |
rs577646065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176114176 | CTCAAGTTCCTACGG[C/T]ATATTTCAATTTAAG | 64326 |
rs577687817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176081942 | TGCTGAAATATGAAA[A/G]ACAATAATTCCATCC | 64326 |
rs577691994 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175990628 | TTCCCTTAAATATCA[C/T]AGATTTTCTTTTCAT | 64326 |
rs577695807 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176172918 | GCAGAAAAACACAAA[A/T]AGATGTATCAGGATG | 64326 |
rs577703299 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176083863 | AGAGTAGCTAGCTAA[C/T]GTAAGATTCCTGAAA | 64326 |
rs577707646 | in-del | -/TT | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176185006 | CAGTCACCAGAGCCC[-/TT]TTAAGAAAGCTCTAC | 64326 |
rs577714876 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176115615 | TTAGCTGGGCGTGGT[C/G]GCGCGTGCCTGTAGT | 64326 |
rs577716269 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176071319 | TCCCTAGAAACTGAG[C/G]AGATGCCAGCACCAT | 64326 |
rs577720222 | in-del | -/AATTC | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:176195589 | AAACGAGTCTCTATA[-/AATTC]AAAAGGACTAATATC | 64326 |
rs577722953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176199682 | ACACAAAAGACTACC[A/G]ACTAAAGGACTCCAT | 64326 |
rs577724109 | in-del | -/GTTTGTCTTTCA | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176112815 | CAATATGTGATGTTT[-/GTTTGTCTTTCA]GTTCCTGGCTCATTT | 64326 |
rs577737746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175992986 | CAGCCTAACTAGGAG[A/G]CACCACCCAGTAGGG | 64326 |
rs577747301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176116104 | AAAAAACTGCCAGGG[A/G]TAGTGATTTTCACCT | 64326 |
rs577754499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176153466 | TTTGCTGAACTTGTT[C/T]GTCAGCTTAAGAAGC | 64326 |
rs577756667 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176063207 | TGGGACTACAGGCGC[A/C]CGCCACCGCGCCTGG | 64326 |
rs577760984 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176139258 | CAGAATGGCAATTAT[C/T]GAAAAGTGAAAAAAC | 64326 |
rs577765347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175982088 | GGGAATGTAAATCAG[C/T]ACAGCTTTTATGGAA | 64326 |
rs577777249 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RFWD2 | GRCh38.p7 | 1:175974747 | GTTAAGGAAAGAATA[C/T]GTGGGCCAGGCATGG | 64326 |
rs577780671 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176007195 | GGTTTTCAGCTCCAT[C/G]AGCTCCTTTAAGCAC | 64326 |
rs577789531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176200284 | TGTCAGTACAACACA[C/T]TCCATCTTCACTTGA | 64326 |
rs577799769 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176153804 | TAATATGAAGGAGGG[C/G]TGAATTTTGTTGAAA | 64326 |
rs577808869 | in-del | -/TTGA | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175970899 | GGTAACAAGCAATGT[-/TTGA]TTGATTATCTCTGTA | 64326 |
rs577818714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176083124 | CCCAACTGTACTGCA[A/G]AGTGGTCTGGATATA | 64326 |
rs577837079 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175998969 | TATGCTCCAGTACTT[G/T]CAAAGCAGAGCACAA | 64326 |
rs577862773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176138304 | GGTAGAAAACACCAA[C/T]GTTAAAGAGATGGGC | 64326 |
rs577875226 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176110879 | AATTTATCAGCAGGG[C/T]GCAGTGGCTCATGCC | 64326 |
rs577883472 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176021386 | GTACAAACTCAGCAG[G/T]TGCCAAATTATCTAA | 64326 |
rs577883681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176070793 | ATTAGGACTACAGGT[A/G]CACACCACAGGCCTG | 64326 |
rs577918669 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176006887 | TTTCCTGAATCTGAA[C/T]GTTGGCCTGCCTTGC | 64326 |
rs577919243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176205097 | TACTTTATTTTAGTG[C/T]ACTTACACGGAGGCT | 64326 |
rs577923925 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175958388 | TCAGGTATAATATCA[A/T]AGCCATTTCAGCTAT | 64326 |
rs577935264 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176112156 | ATTTACGTACTGTCT[C/T]AGTGCACTATCTCAA | 64326 |
rs577935301 | snp | C/T | 0 | 0 | intron-variant | RFWD2 | GRCh38.p7 | 1:176105532 | ATGCAAATAAGTAAG[C/T]GTATTTTGATCGTGA | 64326 |
rs577956164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175979990 | TTAAAAATATAATAC[C/T]AATAGCAAACATGTA | 64326 |
rs577964781 | snp | A/G | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176186607 | AGACTTCGGCTTTTA[A/G]GTTGAGTAAAACGGT | 64326 |
rs577980161 | in-del | -/ACACAC | 0.0830669 | 0.1861 | intron-variant | RFWD2 | GRCh38.p7 | 1:176119642 | ACATTATACATTCAT[-/ACACAC]ACACACACACACACA | 64326 |
rs577983858 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | RFWD2 | GRCh38.p7 | 1:176151952 | TGCCATTTTGAGGGC[A/T]TTTTTTTTTTTTTTT | 64326 |
rs577995321 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176206802 | CGGGCCCCCGAGGCC[A/G]CCCGAGCCGGCGGCC | 64326 |
rs577995418 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176169251 | TTGGGGAGAAGGATA[C/T]CACACACCTTGGTAA | 64326 |
rs577997723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176025856 | GATCGTGCCACTGTA[C/T]TCAACCTGGGTGACC | 64326 |
rs578012328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176171950 | AGTAACAAATCACTA[C/T]GACATTTAGATTCCA | 64326 |
rs578016929 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:175978797 | GTTGAAGGAAGACAG[-/A]AAGAAAGAGAAGAAG | 64326 |
rs578025587 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RFWD2 | GRCh38.p7 | 1:176111693 | ACATTTTATTTATAC[A/G]AAAAAAACTGTCTAT | 64326 |
rs578041837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176161384 | GCTTGAAGCCAAGAG[C/T]TTGAGACTACTGTAG | 64326 |
rs578056813 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176075701 | AGAAGACTTAGCCAC[A/C]CAATAATAGTGGGGG | 64326 |
rs578057222 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RFWD2 | GRCh38.p7 | 1:176159166 | ATATACTTGGCAAAG[C/T]AGTAATATACAAAAT | 64326 |
rs578063647 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | RFWD2 | GRCh38.p7 | 1:175986106 | CTCACTGCAAGCTCT[G/T]CCTCGCGGGTTGATG | 64326 |
rs578090577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176145738 | GATAGGAATAAAAGA[C/T]TACATACTGCACAAG | 64326 |
rs578101988 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176047868 | TCCCTTGAGTCCAGG[A/G]GTTTGAGACCAGCCT | 64326 |
rs578104886 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176141523 | ACATACATACATACA[C/T]ACAGCAGCAAAACTT | 64326 |
rs578108576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176097783 | CTGAGGCGGGACAAT[C/T]GCTTGAACATGGGAA | 64326 |
rs578110345 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176093126 | ATATAGGGGTGTGTA[C/T]ATATGTGGTAAAACT | 64326 |
rs578155037 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RFWD2 | GRCh38.p7 | 1:176067909 | CGATCTGCCTGTCTG[C/T]CCCCTCCCCATAGGG | 64326 |
rs578188661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176055192 | TAATCCCATCACTTC[A/G]GGAGGCCGAGACAGG | 64326 |
rs578202284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175973968 | TGCTGGAGTGTAAAA[C/T]GTGCTTATGCAAGTG | 64326 |
rs578205100 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176054817 | TCTTATATTCCTATA[C/T]CTATTTTAGCTACTA | 64326 |
rs578214880 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RFWD2 | GRCh38.p7 | 1:176067083 | AAGAAATTATAAAAA[A/G]TATGATATTATAATG | 64326 |
rs578228716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176104328 | TGTAATTTTTAAAAA[C/T]TGATAATTTTAACTA | 64326 |
rs578241515 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:175973499 | TACAAGTTGCTAAAT[C/G]TTACACATTTTAAAG | 64326 |
rs578246620 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176191532 | CTTCAAAAGCAGCAT[C/G]CAAATTCAACTGGCC | 64326 |
rs578262245 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RFWD2 | GRCh38.p7 | 1:176191977 | ATTCTAAATAACTAT[G/T]TGCTAGCTTCAGGGT | 64326 |
rs745319215 | in-del | -/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176154022 | GGATTTTTGCATGGA[-/T]GTGAATCAGTAACAC | 64326 |
rs745325441 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176124865 | TCCATAGTGGTTGTA[A/C]TAAATTACATTCCCA | 64326 |
rs745325722 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176201009 | AAACATTTTATTTGG[G/T]ATACAGGTTGAATAT | 64326 |
rs745327508 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176059437 | ATTAGAATTAAGACA[C/G]TATAATTTTTTAAAA | 64326 |
rs745330122 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175965414 | CCAATTTCATCACTC[G/T]TGCTGACATTTTGTT | 64326 |
rs745333539 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175947958 | AGTAATTGATGTAAA[A/G]CCTGCCAACATCCTT | 64326 |
rs745349445 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176020511 | TGGTGAAACCCCATC[C/T]CTGCAAAACTAGAAA | 64326 |
rs745365361 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176169473 | TACCTTGGAGAAATC[A/G]CAGGTTCGGTTCTAG | 64326 |
rs745376343 | snp | A/G | 2.12118e-05 | 0.0032566 | intron-variant | RFWD2 | GRCh38.p7 | 1:176027721 | TAAAAACAAAAAGAG[A/G]AACAAGTAATACATT | 64326 |
rs745386734 | in-del | -/TCTC | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176099518 | TTGTCTCTCTCTCTC[-/TCTC]TCTCTCTCTCTCTCT | 64326 |
rs745397807 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176120586 | AGTGAGAAGCTTTGC[C/T]AAAAAAAGTAACAAC | 64326 |
rs745410336 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175949617 | CTCACTGATCAACCT[A/C]GTTGCCATTCAAGGA | 64326 |
rs745421820 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176030556 | TTGTAATTTCATGGT[A/C]ATTTTCTCAATGCAG | 64326 |
rs745425567 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175986101 | CTTGGCTCACTGCAA[C/G]CTCTGCCTCGCGGGT | 64326 |
rs745434058 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175984232 | CAGGTCCAGGGTTGG[C/T]ATGCTGCGTGCAGCC | 64326 |
rs745435487 | snp | C/G | 1.6486e-05 | 0.00287102 | intron-variant | RFWD2 | GRCh38.p7 | 1:175947190 | AGATATAGTAAATAG[C/G]TTACCTTAATTGTAC | 64326 |
rs745440390 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176001898 | TCTTTTCCTTTCAAT[A/G]CTTTAAACATATCCT | 64326 |
rs745465581 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176182572 | TTATCTGGTCTAATA[C/T]GTCAATAGTGACAAG | 64326 |
rs745477831 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175988678 | TCTCTACTAAAAATA[C/T]AAAAATTAGTCGGGC | 64326 |
rs745479899 | snp | A/T | 1.73586e-05 | 0.00294601 | intron-variant | RFWD2 | GRCh38.p7 | 1:176206540 | AGAAACTCATAATTT[A/T]GGGACAAGGAGGGAG | 64326 |
rs745481639 | snp | G/T | 1.6486e-05 | 0.00287102 | missense | RFWD2 | GRCh38.p7 | 1:176116667 | TGGCTGTATTCTGTG[G/T]AATCAATAATACTAC | 64326 |
rs745491927 | in-del | -/TGTG/TGTGTG | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176127565 | TAGTATTCTACTGTG[-/TGTG/TGTGTG]TGTGTGTGTGTGTGT | 64326 |
rs745494965 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176084896 | TTAAGCAGATGCCTC[A/C]TTAATGACCTGAATT | 64326 |
rs745496397 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176135540 | CAAAAAACACCCAGA[A/G]TATGTCAGTCTCTGC | 64326 |
rs745518364 | snp | A/G | 1.64874e-05 | 0.00287113 | synonymous-codon | RFWD2 | GRCh38.p7 | 1:176027585 | ACCTGCACAGCCGAA[A/G]GCCAAATGGTATCTG | 64326 |
rs745518485 | in-del | -/TTTTTCC | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176041354 | TTTTTCTTTTTTTCT[-/TTTTTCC]TTTTTTTTTTTGAGA | 64326 |
rs745525798 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176050381 | CCAAGCAGTGAATTT[G/T]GTCAGTGTTTCCAAT | 64326 |
rs745529919 | snp | C/T | 1.65573e-05 | 0.00287721 | intron-variant | RFWD2 | GRCh38.p7 | 1:176134985 | TAATATGAATTCTAA[C/T]CAATTGCAAGTGTGA | 64326 |
rs745583024 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176152568 | TTCTTCTGCCTCGGC[A/C]TCCCAAGTAGCTGGG | 64326 |
rs745598286 | in-del | -/TTTG | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176106037 | TGTTTTTTGTTTTGT[-/TTTG]TTTGTTTTTTTGAGA | 64326 |
rs745641818 | snp | C/T | 1.70598e-05 | 0.00292055 | synonymous-codon | RFWD2 | GRCh38.p7 | 1:175986955 | TACCCCATCTGGTAG[C/T]GCCCTCCAGCACACA | 64326 |
rs745662630 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176128964 | TCTACTATATAAAGA[A/G]TCATCCCTGTCCTCC | 64326 |
rs745666694 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176143762 | GACACCCCTGGGCCA[A/G]TCAGGATGGTTGGTC | 64326 |
rs745698802 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176095795 | TAGCACAAATAAAGG[C/T]AACAGCACCAAATCC | 64326 |
rs745715069 | in-del | -/TTAG | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176029252 | ATATTCTAGAATTAT[-/TTAG]TTAGTTAAATTGCAA | 64326 |
rs745727210 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176061377 | TCACGCCTGTAATCC[C/T]AGCACTTGGGAGGCC | 64326 |
rs745731481 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176189131 | AAAACCTTAAAGGCA[G/T]CCCTAGAAAGACACA | 64326 |
rs745737408 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175990592 | AGTATTTTTCAACAA[C/T]TTCAGTCAAAATATC | 64326 |
rs745748433 | snp | G/T | 1.66724e-05 | 0.0028872 | intron-variant | RFWD2 | GRCh38.p7 | 1:176046160 | CTATACTGCATCATG[G/T]CAAGAAAATAATGTA | 64326 |
rs745761605 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176190884 | GTAGTACTGGTTCCA[A/G]CTAAAAAAAAAATCA | 64326 |
rs745762852 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176002134 | TGATGTTTTCCATCC[A/C]ATTTGCAAAAATACT | 64326 |
rs745773575 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176108928 | ACCATCCTGTCCAAC[A/G]TGGTGAAACCCCTTC | 64326 |
rs745792162 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176059954 | GTTGAAATTTGACTC[A/G]CAGGTATTAGTTTGC | 64326 |
rs745801732 | snp | A/G | 1.86757e-05 | 0.00305573 | intron-variant | RFWD2 | GRCh38.p7 | 1:176046351 | AAGTATGTAATGACA[A/G]CATTTCAGAATTTGC | 64326 |
rs745807673 | snp | G/T | 0.000171954 | 0.00927079 | intron-variant | RFWD2 | GRCh38.p7 | 1:175982390 | CAAATTTTCTTCCTC[G/T]TCTACCACTCCAGAG | 64326 |
rs745835198 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176157179 | AGCCTGAGTGACAAA[A/G]AGAGACTCCATCTCA | 64326 |
rs745861513 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176122284 | ACATCATGTTTTAAC[A/G]CTGAAATATTAATGT | 64326 |
rs745872204 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176076512 | CTAAAAATGCCTTCA[C/T]CAAGAGGTTAGGAAG | 64326 |
rs745919315 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175982893 | GAGTGGGAGGATGCC[A/G]AGATGTTGGTCCAAG | 64326 |
rs745927140 | in-del | -/TT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176050180 | GAAACATTTCAACTG[-/TT]TTAAAAGAGTGATTT | 64326 |
rs745929717 | snp | C/T | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176186477 | GCACAGCAGGCGAAG[C/T]TGCAGTGAACAGAGA | 64326 |
rs745938228 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176095545 | AAATAAGCTGGGCAT[G/T]GTGGCATACACCTGC | 64326 |
rs745951357 | in-del | -/TAAAT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176196012 | CATGTACAGGTAAAA[-/TAAAT]TAAACAACATACTTC | 64326 |
rs745953751 | in-del | -/TAG | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176076596 | ATCTAATCCCAAAGC[-/TAG]TAGTAGAAGAAAAAA | 64326 |
rs746032953 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176154110 | GCTGGCCTCACAGAA[C/T]ACTTAGGGAGGAGTG | 64326 |
rs746044202 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176138359 | CAAGAAGGGCAAAGT[C/T]GCAGCCAGAAAACCA | 64326 |
rs746050326 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176025707 | ACAGCCTGAGCAACA[C/T]GGCAAAACCTCATCT | 64326 |
rs746103176 | in-del | -/AAAC | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176139286 | ACAAAAACAAAAAAA[-/AAAC]ACAAAAAAAAAAAAC | 64326 |
rs746123394 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176121968 | ACACAGTGAAACCCC[A/G]TCTCTACTAAAAATA | 64326 |
rs746128120 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175987883 | TGCTATGCAAACAGA[C/T]TACTTCATGAAGAGA | 64326 |
rs746158808 | snp | C/T | 1.66095e-05 | 0.00288175 | synonymous-codon, intron-variant, missense | RFWD2 | GRCh38.p7 | 1:176149030 | ATTTCTTCTTGCAAC[C/T]TTGAGGAATTCCATA | 64326 |
rs746183763 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176047768 | ATGATGGTAAGTAAG[A/G]AAAAGACACATTAAG | 64326 |
rs746183852 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176066691 | ATCACCAAGATGAAA[C/T]ATCAGTTATTTTAAA | 64326 |
rs746206446 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176193522 | AAACAGCCCAAATTG[C/T]CCATCAACTGAAATA | 64326 |
rs746210737 | snp | A/G | 6.88978e-05 | 0.00586891 | intron-variant | RFWD2 | GRCh38.p7 | 1:175988456 | TACTTAAAATTTCTT[A/G]GCACGAAACTCATCA | 64326 |
rs746217043 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176147538 | GAAGTATTTGGAACT[A/G]GTATGTTTCTTGGTT | 64326 |
rs746220451 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176111165 | TCAAAAAATAAAAAT[-/A]ATAATAATAACAGTA | 64326 |
rs746234797 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176113332 | ATACCTATTGACCAC[C/T]TGTATATCTTCTTTT | 64326 |
rs746236381 | snp | C/T | 1.65181e-05 | 0.00287381 | missense | RFWD2 | GRCh38.p7 | 1:176085871 | GCTAACGTGCTATTA[C/T]ACCAAGGCTGTTTCT | 64326 |
rs746249530 | in-del | -/T | 0.000195561 | 0.00988646 | intron-variant | RFWD2 | GRCh38.p7 | 1:176133823 | TTGTGATGTGACAAC[-/T]TTTTCTTCCCTGTAT | 64326 |
rs746255942 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175961430 | TCCGTCCATTAGGGT[A/G]GATATCACATGCCAG | 64326 |
rs746271740 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176065454 | TTATGTTATAAAACA[C/T]TTGTCACCAGATTAA | 64326 |
rs746281451 | snp | A/G | | | downstream-variant-500B | RFWD2 | GRCh38.p7 | 1:175944383 | ACATTACTCAGCCTA[A/G]GATGGTACTAAAAGC | 64326 |
rs746296028 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176192750 | AGTATAAGAAAATAT[A/G]AACAGGGTACCATGT | 64326 |
rs746301363 | in-del | -/GGG | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176168512 | GAAGGAAGGGAGGGA[-/GGG]AGGGAGGGAGGGGAA | 64326 |
rs746313275 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176072088 | TGAATTACCATAGAA[G/T]TAGAAAACTCACCAA | 64326 |
rs746321962 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176037889 | AACAAAGCAAGAAAG[G/T]TTCACTGTTGTCATT | 64326 |
rs746324265 | in-del | -/AAC | 7.08173e-05 | 0.0059501 | intron-variant | RFWD2 | GRCh38.p7 | 1:176163766 | TATTAAACCAATAAA[-/AAC]AACAAAATGAAATTT | 64326 |
rs746327878 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176038211 | TGCGAAACTTGCATG[C/T]TGAAAATGACAAAAC | 64326 |
rs746336083 | snp | A/C | 1.69697e-05 | 0.00291283 | missense, intron-variant, utr-variant-5-prime | RFWD2 | GRCh38.p7 | 1:176163861 | CTCTTTTCCTCAAAT[A/C]TTTGCTTCTGTTTAA | 64326 |
rs746356536 | in-del | -/AA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175961697 | TGAGACCCTGTCTCA[-/AA]AAAAAAAAAAAAAAA | 64326 |
rs746372195 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175981817 | AACCCACTTAAAAAA[C/T]AAGCAAAGAACCTGA | 64326 |
rs746372310 | snp | A/T | 1.75718e-05 | 0.00296405 | intron-variant | RFWD2 | GRCh38.p7 | 1:176085737 | GAAACAGATCTGAAA[A/T]GTAGATTTCAGATAA | 64326 |
rs746377327 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176078234 | GCATCACACTACCCA[A/G]CTTCAATTTATACTA | 64326 |
rs746389898 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175998884 | CAATAATGGAATGGA[A/G]CTTCATTGAGTGGTA | 64326 |
rs746395782 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176205699 | CAAGACAATCAACAC[A/C]ACCTTTCACTTCATA | 64326 |
rs746399646 | in-del | -/TT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176054162 | CTCAGCAAATTATTC[-/TT]TTTTTTTTTTTTTTG | 64326 |
rs746399792 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176200854 | AATGCTTACAGAATT[C/T]TGTCCTACATACAAC | 64326 |
rs746405959 | in-del | -/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176106733 | CCTTAAAAATTCTTA[-/T]CCCCAAATGCTCGGG | 64326 |
rs746407292 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175945628 | TTCATCCATTTCTAG[C/T]CAATCATCTAGCGTC | 64326 |
rs746415934 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176039624 | ATAGAATTTCAAGAG[A/T]TCCCAAATAACTGAA | 64326 |
rs746443977 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176084773 | GATCTAAGCAATATG[C/T]AGATTATAAATAATA | 64326 |
rs746446872 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176125248 | TTTGGTGTGCAGAAG[C/G]TTTTTAACTTGATAT | 64326 |
rs746479978 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176194037 | AATGGAAATACACTA[C/T]TGCAAAATTTTTATA | 64326 |
rs746491858 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175962497 | CCTTTAAATTTGTCT[G/T]CTTGTCTAAATGGTA | 64326 |
rs746501529 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176033327 | AGCTACTTGGGAGGC[C/T]GAGGCAGGAGAACTG | 64326 |
rs746503630 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176017786 | CACCTCGGCCTCCCA[A/G]AGTGCTGGGATTAGA | 64326 |
rs746514995 | in-del | -/TCTCTCTCTCTCTCTC | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176099506 | TTTGGAGCATATTTG[-/TCTCTCTCTCTCTCTC]TCTCTCTCTCTCTCT | 64326 |
rs746518653 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176032526 | GTAAGCTGGGTAGTT[G/T]TGGCTCAGTCTCAAC | 64326 |
rs746526584 | snp | A/G | 1.64844e-05 | 0.00287087 | missense | RFWD2 | GRCh38.p7 | 1:176116649 | CCACTGAAACCTGGA[A/G]GTTGGCTGTATTCTG | 64326 |
rs746548485 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176099728 | AGCTCGACTTGCAGA[A/G]CCAATAAAAGCCCCT | 64326 |
rs746558593 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176008204 | GCCCTGCATCAGCTC[A/G]CGCACGGTGCACGCA | 64326 |
rs746582354 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176193470 | AACTCATACACAAAT[A/G]TTCACGGGAACATTA | 64326 |
rs746593241 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175965351 | AGATATAGGGATTCT[C/T]AAATTTTTCTTTGTT | 64326 |
rs746605436 | snp | A/C | 4.96422e-05 | 0.00498183 | missense, intron-variant, utr-variant-5-prime | RFWD2 | GRCh38.p7 | 1:176175936 | GGATACAGATGGTCA[A/C]TATTGTCCACAACAT | 64326 |
rs746639435 | in-del | -/AA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176042732 | TGAAACTCTATCTCA[-/AA]AAAAAAAAAAAAAAA | 64326 |
rs746656137 | snp | A/C | 1.68627e-05 | 0.00290363 | intron-variant | RFWD2 | GRCh38.p7 | 1:176085923 | GACACAAAACTTAGA[A/C]TAAACAATACTCTTC | 64326 |
rs746656874 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175947652 | TGGGATTACAGGCGT[C/G]AGCCACTGTGCCCAG | 64326 |
rs746671778 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176065257 | TGTGAACAGTAGATA[A/G]AGAAATTAACTCAGA | 64326 |
rs746674027 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176192724 | GCTATAAAAACAGGA[A/G]TTTCTATTACAGTAT | 64326 |
rs746694013 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176000354 | CATTTATTGAAAAGA[C/T]TGTCTTTTCTCCAGT | 64326 |
rs746722902 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176160899 | AGGGGTTAAAAATTA[C/T]AGTTTTCTCCTAAAG | 64326 |
rs746726443 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176111676 | CTACTTTTGGAAAGT[A/G]TACATTTTATTTATA | 64326 |
rs746749004 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175969197 | CCTTTTAGACATTCA[A/G]TTTCTCCAAATATAA | 64326 |
rs746803056 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176047587 | AATATCTATGTATGT[A/G]TGTTTCTTCTCTCAA | 64326 |
rs746818665 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176080209 | AAAAAGAAAGCTAAA[A/G]TAGTACTTTGAACTA | 64326 |
rs746830170 | snp | G/T | 0.000171866 | 0.0092684 | intron-variant | RFWD2 | GRCh38.p7 | 1:175982347 | CCTTGGAAAACACAG[G/T]TTTGAACTGTGAGGA | 64326 |
rs746838949 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175954087 | AAGGGCTAAAATCAT[A/G]CAAGTATGTTCTCTG | 64326 |
rs746852108 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176059041 | TAACACCAGCACTGC[C/G]CTCTAACTTCAAGGG | 64326 |
rs746853651 | in-del | -/AGAAC | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176119311 | TATTTAGAGGCCTAT[-/AGAAC]AGAACATTTCCAGCT | 64326 |
rs746858441 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176050896 | CTATGCTCTCAATCA[C/T]CATGCAAACTTGCAA | 64326 |
rs746858455 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176022749 | TTCAGACCGAGGAAA[A/G]TTAGCTCATACCTAA | 64326 |
rs746870408 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175987720 | CTTTGCTGAACAAAG[C/G]CCAAGTCATTTAAAA | 64326 |
rs746885726 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176155539 | ACTAGAAACCTACAG[A/G]GAAAGGAAGGAGAGC | 64326 |
rs746893341 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176106379 | AACAGCCCTTTCCCC[A/G]AAACAAACCTCCTTC | 64326 |
rs746900385 | snp | A/C | 1.66696e-05 | 0.00288696 | splice-donor-variant, intron-variant | RFWD2 | GRCh38.p7 | 1:176149005 | ACACAAAATAATATA[A/C]CTCTCTCTTATTTCT | 64326 |
rs746912803 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176047465 | GTTTCAGAGCTGGTG[C/T]TAATAATTACTATGC | 64326 |
rs746921634 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176120469 | AAGACATCAAAAAAC[A/G]TCAAGGGAAAAAAAT | 64326 |
rs746942741 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176168197 | CGAGTAGCTGGGATT[A/G]CCGGTGCGCACCACC | 64326 |
rs746947303 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175983194 | GATGGCTTAAAGGAA[A/T]GAAAAAGACTCCTCT | 64326 |
rs746952364 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176065393 | TATATGGGGAAGTTA[C/T]CATACCTAGGACAAA | 64326 |
rs746978933 | snp | A/G | 1.6516e-05 | 0.00287362 | intron-variant | RFWD2 | GRCh38.p7 | 1:176043822 | CAACTGATACAGCTG[A/G]AAGAAATACAGTTAA | 64326 |
rs746979613 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176032279 | GGGGCAATGTGTATT[C/G]TTTTATACCTCTATA | 64326 |
rs747006930 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176135333 | ACTAAATATTGTTCA[A/T]CATTAATGAAGCCAC | 64326 |
rs747023152 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176089883 | CATATTTTGAAATGA[A/T]CCTGCAAAGCAGTCT | 64326 |
rs747024948 | in-del | -/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176164839 | GACACAAAAAACTGA[-/T]TTTTTTTTTTAAAAA | 64326 |
rs747039318 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176053860 | CTGTTACCATTTTCA[A/T]TCTCTTATTTTTTGT | 64326 |
rs747055575 | snp | C/T | 1.70988e-05 | 0.00292389 | intron-variant, synonymous-codon, utr-variant-5-prime | RFWD2 | GRCh38.p7 | 1:176136491 | TTGATTCCTTACTTC[C/T]ACTCTCTTAATATCC | 64326 |
rs747059700 | snp | C/G | 0.000107544 | 0.00733216 | missense, utr-variant-5-prime, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176206738 | GGCCCGTGGACACCG[C/G]CCCGCCGCCGCTACC | 64326 |
rs747088912 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176152719 | GTGCCGTAATTACGG[C/T]GTGAGCCACTGTGCC | 64326 |
rs747093265 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176197982 | ACTGAAAAGCATAAA[C/T]ACTGCTAAGAGAAAT | 64326 |
rs747128783 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176196293 | AAAATGAACAAACTA[C/T]ATAGAAAATCAATAA | 64326 |
rs747129186 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176052837 | ACTGATTTGCACTTG[C/T]TTTTCTCCCCCTCAT | 64326 |
rs747130859 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176069222 | AGAAAAGAAATTATA[G/T]GTAATACAGTAATAC | 64326 |
rs747136010 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176116799 | TTTCTAAGCCAAGAA[A/G]ATATTTATTGCCAAT | 64326 |
rs747145588 | snp | A/G | | | intron-variant, downstream-variant-500B | RFWD2 | GRCh38.p7 | 1:175966997 | AAGGAACACTTTCAA[A/G]ATCAGTTAATCCCAA | 64326 |
rs747155706 | in-del | -/ACTT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176143214 | CTGGTGACATTAAAA[-/ACTT]AAGACTCTATTAAGA | 64326 |
rs747169817 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176039344 | ATAGCACTGAATACA[C/T]ATATTAGAAGATCTA | 64326 |
rs747191106 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175999569 | CAGTGCCGCAAAAAA[A/C]ATGGGAATGCAGATA | 64326 |
rs747191533 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176022613 | CTGAATATCGGTCAG[C/T]TTTCTAGTTGTAAAG | 64326 |
rs747205483 | snp | A/T | 6.81037e-05 | 0.005835 | intron-variant | RFWD2 | GRCh38.p7 | 1:176081303 | CTATATGAAAAAAAA[A/T]AAAAAAAGACAAAAC | 64326 |
rs747216711 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176187576 | TTTTAATCACAGTTC[-/A]TACCCCACAGCTTTC | 64326 |
rs747226683 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176024197 | CGGGGAGGCAGAGGT[C/T]GCAGTGAGCCAATAT | 64326 |
rs747246162 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175975559 | GGATTATAAGCATGC[A/G]CCAATATGCCAGGCT | 64326 |
rs747254052 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176164199 | TTCACCATGTGAGAC[C/T]ATCACATGCCCCATA | 64326 |
rs747281966 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176064085 | AAAGTATAAAAACCA[C/T]CTGTACCTGACGGAT | 64326 |
rs747294383 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176130297 | CTCATAATCACCCTC[C/T]CATACAAAAGAACCA | 64326 |
rs747294868 | snp | A/G | 5.4254e-05 | 0.00520807 | missense, utr-variant-5-prime, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176206668 | CCGCTGCCTAGGCTG[A/G]AGCTGCTGCCTCCTA | 64326 |
rs747297398 | in-del | -/AG | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176091954 | AGAATACTAACTAAA[-/AG]AGAAAAAATAGATTC | 64326 |
rs747315852 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176114414 | TCATCCAAGTTTGGA[C/G]ACAAGAAAAAGAAAA | 64326 |
rs747316205 | in-del | -/T | 1.76858e-05 | 0.00297365 | intron-variant | RFWD2 | GRCh38.p7 | 1:175986904 | ACATAATGCATAATA[-/T]TGAGATCCCAAGGTG | 64326 |
rs747327843 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176205590 | AAGGAAAGTACGAAA[C/T]ACTACCACTTCTTAA | 64326 |
rs747340341 | snp | C/T | 1.64836e-05 | 0.0028708 | missense | RFWD2 | GRCh38.p7 | 1:176081251 | TTGGACAAGCATTCC[C/T]GAAATTCATCCAACT | 64326 |
rs747347385 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176124998 | CATTGTAGTTGTGAT[C/T]TGCATTTCTGATGAT | 64326 |
rs747372100 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176173440 | CAGGAGTTTGAGACC[A/G]GCCTGGAAAACATAG | 64326 |
rs747394556 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176110160 | TGTCTTAGATTCAAC[C/T]AATTTTTCGAAATTC | 64326 |
rs747396862 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176154589 | ACTAAACGATGAGGA[C/T]ACATGGACACATAGA | 64326 |
rs747415879 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176204556 | GTTTTAAATCAGATT[C/T]TCATTAATTAATTCT | 64326 |
rs747446336 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176014842 | AAATACATGTATTTA[C/T]TGAAAATCTATTATG | 64326 |
rs747446948 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175958979 | AAGTTAATATACCCA[C/T]GAAATCAAAACCTGA | 64326 |
rs747463588 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175960162 | ACCAGAATTTATATA[C/T]GACAATCTGTATTCC | 64326 |
rs747482432 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176043924 | ATTTTAAAATGGTCT[C/T]TATCAGTTCACAATC | 64326 |
rs747498078 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176075446 | ACCAAATTCCCGATA[C/T]GCCTCAAAAAACATC | 64326 |
rs747500109 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176091051 | AAAATGCTTTTCAAG[A/G]GCAGTAGAAAGAAGC | 64326 |
rs747513935 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176123901 | ATTTTCTAAAGTAGC[A/G]TCTCTACCACTCCCA | 64326 |
rs747530209 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175949370 | ACCTGAATGTAGAAA[A/G]TGGTTGGAGTAGGTT | 64326 |
rs747534655 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176016418 | TACTACTGAGAGATC[A/T]AATGAAATAAGGGCT | 64326 |
rs747541659 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176098267 | ATTTACCAGGTTTTA[A/G]AGGTAAAATTGCTAA | 64326 |
rs747547719 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176199144 | AACACAGTGAAACCC[C/T]ATCTCTACTAAAAAT | 64326 |
rs747550223 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176171408 | TAGGGTCTTGTTCTG[C/G]ATAAGACTTTGGCTT | 64326 |
rs747552246 | snp | C/G | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176185291 | TAGGCACAGTTTATA[C/G]ATGAGGGAACAGAAG | 64326 |
rs747564934 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175988916 | GTGTAAAAGCCAACC[A/T]AGTAATATTTAAAAC | 64326 |
rs747578371 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175987469 | AACCAGAAATATATT[A/G]TAAGAATCTTAAATT | 64326 |
rs747579208 | in-del | -/ATAGGT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176128888 | GACAATGCATTGGTC[-/ATAGGT]AATAATCCAGCCAAA | 64326 |
rs747590286 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176192467 | ACTACCCGCTTACAA[C/T]ATACAGCCCCTTCAG | 64326 |
rs747599895 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176138153 | AGGCATGACAGAATA[A/C]GCAGAGTAAATAATA | 64326 |
rs747624447 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176170729 | AAAGTCACCAGCTGC[A/G]TCAACCCCTATCAAG | 64326 |
rs747651198 | snp | G/T | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176145572 | ATAGTAGTATTTTTT[G/T]GCCAACAGCCCCAAA | 64326 |
rs747652233 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176030663 | TTCAATATAACTGTC[C/T]GAGCTACAAGGGTAA | 64326 |
rs747664869 | snp | A/G | 3.38186e-05 | 0.00411195 | intron-variant | RFWD2 | GRCh38.p7 | 1:176175892 | ATTTTTAAAATAAAA[A/G]TCATTCCAAAGACTC | 64326 |
rs747672046 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175974753 | GAAAGAATACGTGGG[C/T]CAGGCATGGTGGCTC | 64326 |
rs747675959 | snp | A/G | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176145917 | CAGGGTGCTTCAGCC[A/G]TTCTAGCAGTATTGC | 64326 |
rs747680708 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176205379 | AAGGTGAATAAAGAC[A/T]TCATTTTTCTGCAGG | 64326 |
rs747689088 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176002276 | CTTTTATTCTTTTTT[A/C]TTTGTATTCTTTACA | 64326 |
rs747711793 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176097159 | CAGCTTAATTAAAAG[C/T]AGATATCCAAGTTGT | 64326 |
rs747715922 | in-del | -/AC | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175963949 | GAACTAAAAACAAGT[-/AC]AGTTGTCCAGTTATG | 64326 |
rs747732430 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176113569 | GTGTTAATATAAATG[G/T]TAACTGTGGAAACCT | 64326 |
rs747734434 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176159911 | TAAGACATACGCCAA[A/G]ATCTTCACATTTATT | 64326 |
rs747736858 | snp | C/G | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176144259 | TTAACCAGGTTGCTG[C/G]ATATTTTTAAAAATC | 64326 |
rs747739582 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176031991 | CAAGGTTTATGTTTC[C/T]GAGTTTCTCTGACAG | 64326 |
rs747749658 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176061718 | AAATAGATTATAAGC[C/T]TGTAAGTAAAAGCTA | 64326 |
rs747762593 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176191001 | GCAGTAGTTACACCT[C/T]ACATAAACAGGACTG | 64326 |
rs747817945 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175972370 | GGTCAGGTGGCTAGT[A/G]AGAGGGAAGTGAGGA | 64326 |
rs747826759 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176158784 | AGCTGGGACTATAGG[C/T]GCACACCGCCATACC | 64326 |
rs747850647 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176204220 | TCTGTGCCTCAATGA[A/G]AAAATAATTAGTATT | 64326 |
rs747857962 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175966973 | GGGAATTGGGATTTC[C/T]TCATCACAAAGGAAC | 64326 |
rs747858405 | in-del | -/A | 3.82241e-05 | 0.00437157 | intron-variant | RFWD2 | GRCh38.p7 | 1:176163910 | AAACAGAAACAAAAT[-/A]AAAAAGCACACATAA | 64326 |
rs747858988 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176172239 | TAGAGACAAGGTCTC[A/G]CTATATTGCGCAGAC | 64326 |
rs747868531 | snp | A/G | 1.82091e-05 | 0.00301732 | intron-variant | RFWD2 | GRCh38.p7 | 1:176163894 | ATGAGTTCATTCACT[A/G]AAAACAGAAACAAAA | 64326 |
rs747884349 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176025874 | AACCTGGGTGACCCT[C/G]TCTCATAAAAACAAA | 64326 |
rs747892307 | snp | A/G | 1.67393e-05 | 0.00289299 | intron-variant | RFWD2 | GRCh38.p7 | 1:176148988 | AAAACATTATGTAAA[A/G]CACACAAAATAATAT | 64326 |
rs747914717 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176199549 | TAACTAGCAAATATA[C/T]AAGCAGTTCATGTTA | 64326 |
rs747937545 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176124117 | CTTTTTAATTTTTTT[A/T]AATTTTTAGTGTTTC | 64326 |
rs747959330 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176154250 | CTGTTCAGGGATTCA[A/G]TTTCTTCCTGGCTCA | 64326 |
rs747967724 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176053851 | CTTTGCACTCTGTTA[C/T]CATTTTCATTCTCTT | 64326 |
rs747973277 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176104682 | GAGGTGCTGTGGGGA[A/G]AACAGACATATTTAC | 64326 |
rs747973787 | snp | C/G/T | 4.96934e-05 | 0.00498444 | intron-variant | RFWD2 | GRCh38.p7 | 1:176043289 | GCAGAAAGAAGACAG[C/G/T]AGCCTCAGATAGAAT | 64326 |
rs747984426 | snp | C/G | 1.80713e-05 | 0.00300588 | intron-variant, downstream-variant-500B, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175968361 | ATACTGAATAAAATG[C/G]CAAGGAAACCAAGTA | 64326 |
rs747985015 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175985550 | GTAATCACCCATACA[A/G]CGTCAGGCACTGAGC | 64326 |
rs748001071 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176198213 | AATAAAGGATAAAAA[G/T]TACACTACCTGATTT | 64326 |
rs748010962 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176008934 | CTTAATGCTTTGCAC[A/G]ATTTGTGTGTATGTT | 64326 |
rs748026413 | in-del | -/TG | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176127604 | GTATGTGTATATATG[-/TG]TGTGTGTGTATATAT | 64326 |
rs748026453 | in-del | -/ATC | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176160688 | AACTCAACATCACTG[-/ATC]ATTAGATAAATGCAA | 64326 |
rs748028739 | snp | A/G | | | intron-variant, utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175967857 | TGTGGCCCCTTAGAA[A/G]AATAATATTTCTTTT | 64326 |
rs748077785 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176133560 | ACACACATCCCAAAA[C/T]GTAAGCTCCAAAGGG | 64326 |
rs748104913 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176009767 | TAATTAGAATTTGTT[C/T]TGAGTTATAGTTACT | 64326 |
rs748112877 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175952711 | CTCAGGAGTTTGAGA[C/T]CAGTCTGGGCAACAG | 64326 |
rs748123420 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176149332 | TGAAAAATCTTTTCA[C/T]GGATAATGGCAATTC | 64326 |
rs748139011 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176045282 | ATCCTCTTCACTTAG[A/G]ACATAAACTATAACA | 64326 |
rs748147751 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176113908 | TAAAGTTTTAACCAG[C/T]AAAGAAGCAGCAACC | 64326 |
rs748160868 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176113715 | TGAGAGATGGCTCAG[C/T]AAGACAGTGTTAGAA | 64326 |
rs748164640 | snp | A/G | 1.67697e-05 | 0.00289561 | intron-variant | RFWD2 | GRCh38.p7 | 1:175988273 | AAAGTTCCTGGAAAC[A/G]ATGGTTTCACTTACC | 64326 |
rs748168916 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176044232 | TATAAGCCAAATAAA[C/G]TACAGTGAATTGGGT | 64326 |
rs748188959 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176206361 | TACCTCTTTATTATC[C/T]CCACCCTGCCTCGCT | 64326 |
rs748216622 | snp | C/T | 1.72436e-05 | 0.00293624 | missense, utr-variant-5-prime | RFWD2 | GRCh38.p7 | 1:176206584 | CACCATACGAAGTCG[C/T]TGCTTTTGTCCTCGT | 64326 |
rs748235552 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176014671 | AAGCTTACAACCTGA[A/G]ATCAAAACTCTATGT | 64326 |
rs748255805 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176163922 | AAATAAAAAGCACAC[A/G]TAATTTGTATTTTTG | 64326 |
rs748260346 | in-del | -/CA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175956849 | AGAAAGCATTGTTAC[-/CA]CATAGGAGATGACAG | 64326 |
rs748262504 | in-del | -/TAATAG | 2.04432e-05 | 0.00319706 | intron-variant | RFWD2 | GRCh38.p7 | 1:175987121 | GAAAACAAATAATAA[-/TAATAG]TATTTTAGAATAGAA | 64326 |
rs748262897 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176162531 | TCCAAATCTCACATA[C/T]GAAGAGGGGACAATA | 64326 |
rs748277782 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176080666 | TTCAACAGCCCTGAT[A/G]AGACGGACAAATGTC | 64326 |
rs748279710 | snp | A/G | | | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176208845 | ACACTTTGGGAGGCC[A/G]AGGCGAGTGGATCAC | 64326 |
rs748304222 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175991633 | TTGACTCTTGTAATA[A/T]CACTTAGCTTAAAAC | 64326 |
rs748308778 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176046664 | TATACTAAAAGTATG[C/T]CAAAAGACAATTATC | 64326 |
rs748311637 | in-del | -/T | 1.82201e-05 | 0.00301823 | intron-variant | RFWD2 | GRCh38.p7 | 1:176081338 | AATTGAACTGCAAAG[-/T]TAAGTCAAAGAGCCA | 64326 |
rs748317543 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175978056 | GCATGGTGAGATTAC[A/C]ATAAAAGTTACTGTT | 64326 |
rs748321659 | snp | A/T | 2.01717e-05 | 0.00317576 | intron-variant | RFWD2 | GRCh38.p7 | 1:176046368 | ATTTCAGAATTTGCT[A/T]TTTTCTATTTCTAAA | 64326 |
rs748347981 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176036729 | CCTGTATTATTCAAC[A/G]TTGTATTGTAAAAGT | 64326 |
rs748353016 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176188880 | AGAACAAAGCATCCC[A/G]GAGTTGTGACATATG | 64326 |
rs748374921 | in-del | -/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176018020 | CCTGCTCTCAATTTA[-/G]GTTGTCAGATCTTTG | 64326 |
rs748376806 | snp | C/T | 1.64819e-05 | 0.00287066 | synonymous-codon | RFWD2 | GRCh38.p7 | 1:176081235 | ATTATATCGAGTAAA[C/T]TTGGACAAGCATTCC | 64326 |
rs748403521 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176020709 | AATTATATTGTGGGC[C/T]TTATCACTGGGAAAT | 64326 |
rs748403791 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176075195 | CCATAATCTGCTGCA[A/T]TTTCAAATTTTACTC | 64326 |
rs748408939 | snp | A/G | 1.65299e-05 | 0.00287483 | synonymous-codon | RFWD2 | GRCh38.p7 | 1:175987027 | GTCGAGAACACTTTT[A/G]ACTGTATCAAACTTA | 64326 |
rs748465109 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176138080 | AAATTTGATTGAAAA[C/T]TAAATCAGAGGCTGA | 64326 |
rs748477215 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176061997 | AAGAGAAAGACCTGA[C/T]TATTATTATTATTGT | 64326 |
rs748484901 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175949384 | AGTGGTTGGAGTAGG[C/T]TCTGGATGTCCTTTA | 64326 |
rs748485274 | snp | G/T | 1.6832e-05 | 0.00290099 | intron-variant | RFWD2 | GRCh38.p7 | 1:176162845 | CATCATTTAAAATTT[G/T]TTTTAAGTTTAGCTA | 64326 |
rs748510844 | snp | C/T | 3.29815e-05 | 0.00406075 | intron-variant | RFWD2 | GRCh38.p7 | 1:175947180 | TTTAAAATGGAGATA[C/T]AGTAAATAGCTTACC | 64326 |
rs748511503 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175984182 | CCTCCCATCACAGGC[C/T]TGGAGACCCCAGAGG | 64326 |
rs748514622 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176053658 | CTTATGACATAACAC[C/T]TTCTGACAACTACTT | 64326 |
rs748516409 | snp | C/G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175984843 | TGGATTTTGGACTTA[C/G/T]ATGGGGCCTGTAGTT | 64326 |
rs748532229 | in-del | -/ATG | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176032702 | CTGCGAAGAGAGAAA[-/ATG]ATGAAGATAGAGGCT | 64326 |
rs748535799 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176026217 | TCATATCTGGCATTG[C/G]TACAAATTAATTAAA | 64326 |
rs748543083 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176027275 | TTGTTTAAATGTTAT[A/T]ATGACCTTATGTTTG | 64326 |
rs748553406 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176152594 | CTGGGATTACACATT[C/T]GCACCACCATGTCCA | 64326 |
rs748573156 | snp | C/T | | | intron-variant, utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175971049 | ACGAAAACAAAGATA[C/T]ATAGAAGACATTTCA | 64326 |
rs748574755 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176159578 | CTAAATGCCCATCAA[C/T]AGAATAATAGATATA | 64326 |
rs748621279 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176022282 | TTACAATTAGCATGA[A/T]GCCTCACTTCCCTGG | 64326 |
rs748670023 | snp | A/G | 1.68241e-05 | 0.00290031 | synonymous-codon | RFWD2 | GRCh38.p7 | 1:176027672 | TGAGTTGTCTAGATT[A/G]GTAGACCACAGCTTC | 64326 |
rs748679874 | snp | A/C | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176176625 | AGAGTTCAAGACCAG[A/C]CTGGGGAACATAGCA | 64326 |
rs748716459 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176101626 | TTTGTTTTACTAGTC[A/G]GGCTTCTGCCCCCAT | 64326 |
rs748724733 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176204014 | GGATAAAACATTTAT[C/G]TCATATGATTATGAA | 64326 |
rs748729808 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176150634 | AGTAACAACTTTATA[C/G]AAAAAGTAACTCCAA | 64326 |
rs748731651 | in-del | -/CTACTGCCT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176001912 | TACTTTAAACATATC[-/CTACTGCCT]GCTGGCAGTAATGAT | 64326 |
rs748742343 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176091507 | CGTCATATCTAGTTT[A/C]TGGGGCTTAAGAATA | 64326 |
rs748749168 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175950872 | TTTTAGTAGCACACG[C/T]AGGCTAGTGAAGAAA | 64326 |
rs748752682 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176155008 | CACATGCTTAAAAGC[A/G]TAAGACGAATATTTA | 64326 |
rs748753445 | in-del | -/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176165361 | GAGAGAGATGTGTGT[-/C]GTGTGTGTGTGTGTG | 64326 |
rs748771935 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176152247 | TCTGGGTGAAAAAGC[A/G]AGACCTTCTCTCTCC | 64326 |
rs748778586 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175985299 | TCTTCTCTTTTACTA[C/T]GTCTGTTTATTTTTT | 64326 |
rs748780753 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176189363 | CTTGCTTTCATTGTT[C/T]CTAGGGACAGTATTA | 64326 |
rs748784809 | snp | C/T | 5.0497e-05 | 0.00502453 | intron-variant | RFWD2 | GRCh38.p7 | 1:176163033 | ACTTCCTATGAAGAC[C/T]GTTTTAGAGACTAAA | 64326 |
rs748814009 | snp | C/T | 1.81109e-05 | 0.00300917 | intron-variant, downstream-variant-500B, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175968349 | CATAACCAGCAGATA[C/T]TGAATAAAATGGCAA | 64326 |
rs748825814 | in-del | -/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176054200 | TGCCTCACTCTGTCA[-/C]CCAGGCTGGGGTGCA | 64326 |
rs748835426 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176029607 | AGGACATTATCCAGA[A/G]AGGGTCCAGGTACTG | 64326 |
rs748866541 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175985936 | AGTCAGAATTTTTTT[G/T]GTCAAAAACCCAACT | 64326 |
rs748870690 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176202592 | AATCCCCGCTGCTTG[A/G]GAGGCTAAGACATGA | 64326 |
rs748897908 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176013721 | TTTATACAAAAGGAC[A/C]TTTTATAGCTGGTAT | 64326 |
rs748900930 | snp | A/G | 3.29669e-05 | 0.00405984 | synonymous-codon | RFWD2 | GRCh38.p7 | 1:175947213 | AATTGTACCCTGACT[A/G]TTAGCAGCAATCAGC | 64326 |
rs748927563 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176199600 | CTAAGCAATTAAAAG[-/A]AAAAAAAACAGTACA | 64326 |
rs748947259 | snp | A/G | 3.30611e-05 | 0.00406565 | intron-variant | RFWD2 | GRCh38.p7 | 1:176043273 | TCTCATGCTCCTGGA[A/G]GCAGAAAGAAGACAG | 64326 |
rs748950432 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175973354 | CTTCTATAGTTTGCA[G/T]GTACTAATCTTTTCT | 64326 |
rs748957517 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176169561 | GTTTACGCTATACCG[C/T]AGTTTAAGTATTATG | 64326 |
rs748993216 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176136836 | AGTGGCTTAAAAAAA[C/T]ACAAGATAGCCAAAG | 64326 |
rs748994949 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175978532 | CCTTCTTATTTCCTT[A/C]CTTTTCTACTTCCCC | 64326 |
rs749003826 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176184007 | AGTTCTAGAGATCAA[C/T]TGTACAATAATATGA | 64326 |
rs749004577 | in-del | -/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176005753 | TTTTACATTTGCTGA[-/G]GAGCTTTACTTCCAA | 64326 |
rs749005618 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176202694 | AAAAAAAATTGGAAA[A/C]CAGTTATATTAACAA | 64326 |
rs749006916 | snp | A/G | 3.48171e-05 | 0.00417221 | missense, utr-variant-5-prime | RFWD2 | GRCh38.p7 | 1:176206632 | TTGCAGAGGGGGGCG[A/G]GGAGAGGTCGCTTCC | 64326 |
rs749073774 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176126517 | GCTGGAGTGCGGTGG[C/T]GCAATCTCAGCTCAC | 64326 |
rs749102821 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176165168 | ATACAGTACTTGTAA[C/T]ATAATGTGATAATCA | 64326 |
rs749103192 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175961963 | GGAGAAAGCAGCTTA[G/T]GTATTAGTTAACGAG | 64326 |
rs749108327 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176028081 | ACTTATTCATTACCA[C/G]GAGAACAGTATGGGG | 64326 |
rs749109390 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176132010 | ATAAACTTCATGAAA[C/T]CTAGTATGTTTTACG | 64326 |
rs749112422 | snp | A/G | 6.61879e-05 | 0.00575235 | intron-variant | RFWD2 | GRCh38.p7 | 1:176184621 | TTATTTTACTCAATA[A/G]AATTGTCTTACCAAA | 64326 |
rs749115984 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176082082 | ACAACGAATCTATTC[G/T]CCAGTCTATTAATAG | 64326 |
rs749143915 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176002054 | CTTTCAAGAGTTTCA[A/G]TATGATGAGTTTAGG | 64326 |
rs749155206 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175962388 | TCACTAACTAGCCCT[C/T]ATCTACCATTAGTTT | 64326 |
rs749169283 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176057085 | GAAATCCATTTTACA[C/T]AGAAAGACAAACTAC | 64326 |
rs749182396 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176020606 | TCGCTCTACCTGTGC[A/G]GTGGAGGCTGCAGTG | 64326 |
rs749185328 | in-del | -/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176033510 | ACAGTCTAAATTCTT[-/C]AAACTCACATTTAAA | 64326 |
rs749205682 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176080846 | AATACCAATTCTATA[C/T]AAACTTACAGAAAAT | 64326 |
rs749215477 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176118359 | CAGTCTTTTTTTTTT[-/A]AGGCATAGTTAATGG | 64326 |
rs749215957 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175949863 | CTTGGGGATAAGCAG[A/G]GAGTCTACTTCTGGC | 64326 |
rs749221357 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176143902 | TGGAGACTACTCAAC[C/G]CCACTCAGAAATTTT | 64326 |
rs749248110 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176109841 | ATATGGGCTTTTTTT[C/T]GGTCTTTCTATATTT | 64326 |
rs749254027 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175966776 | TACATGGAAAATTTG[A/G]TCTTTTATATATCTC | 64326 |
rs749266845 | in-del | -/TTGT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176124520 | AAGTGAAAACATGTG[-/TTGT]TTATCTTTCTGTTCC | 64326 |
rs749269515 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176190817 | TACATGCATATTTTA[C/G]TACAAATGCTAACTC | 64326 |
rs749270608 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176065921 | TCATGCTGGCCAGGC[A/C]GATCTCAAAACTCCT | 64326 |
rs749282195 | snp | A/G | 1.69421e-05 | 0.00291046 | intron-variant | RFWD2 | GRCh38.p7 | 1:175988258 | ACAAACACCTGTTAA[A/G]AAGTTCCTGGAAACG | 64326 |
rs749295219 | in-del | -/T | 0.444444 | 0.157135 | intron-variant | RFWD2 | GRCh38.p7 | 1:176162842 | GTTCATCATTTAAAA[-/T]TTTTTTTAAGTTTAG | 64326 |
rs749299682 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176182202 | CTTCACAATCTATTT[C/G]GTATTTCAACACTTT | 64326 |
rs749299844 | in-del | -/AAAACAA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176110641 | ATATGAGGTATGTTT[-/AAAACAA]AAAACAAAAAACAAA | 64326 |
rs749313346 | snp | A/C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176022607 | AGATGACTGAATATC[A/C/G]GTCAGTTTTCTAGTT | 64326 |
rs749317608 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176091584 | AAAAAAGTTGCATTC[G/T]GGAGCTCTTGTATTG | 64326 |
rs749325955 | snp | C/T | 1.93913e-05 | 0.00311372 | intron-variant | RFWD2 | GRCh38.p7 | 1:176046362 | GACAACATTTCAGAA[C/T]TTGCTATTTTCTATT | 64326 |
rs749328367 | snp | C/T | | | intron-variant, utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175970914 | TTGATTGATTATCTC[C/T]GTATAAAGATGAATA | 64326 |
rs749329301 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176079306 | CATAGCCTTAAAAAA[G/T]AATAAAACCATGTCC | 64326 |
rs749330862 | snp | C/T | | | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207544 | GAAACTCTCGAAAAG[C/T]GACTGCGCAGGCGCG | 64326 |
rs749355550 | in-del | -/TTT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175952992 | ATATTTGATTTCTTG[-/TTT]TTAAGTTTTTTTAAA | 64326 |
rs749359081 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176175381 | CAGGGACTGGTTTCA[C/T]AGAGAACAATTCTTC | 64326 |
rs749366348 | in-del | -/GT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176118346 | TCTGTCTACACAGCA[-/GT]CTTTTTTTTTTAAGG | 64326 |
rs749370756 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176126819 | TCATTCTGTTGATGA[A/T]TTTAGTTCTTATCAA | 64326 |
rs749406939 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176094536 | ACGACACAAATCAAA[C/G]AGAAATATTTATCAA | 64326 |
rs749410454 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176174066 | GCAGTATATTTTTAT[A/G]TTCCTTCCATACTCA | 64326 |
rs749421032 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176140898 | AATCAATAGCAAGCA[C/T]TCTCTTAACACTGTG | 64326 |
rs749428546 | in-del | -/TTGGTGCTAAAAGGTAC | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176025093 | AAGCATAAGCACCAA[-/TTGGTGCTAAAAGGTAC]TTGATAAAATACTGT | 64326 |
rs749429889 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176187649 | GTGACTTTGAGCAAG[C/T]AGTTTAATCTTTCTA | 64326 |
rs749431618 | snp | C/T | 1.65222e-05 | 0.00287417 | missense | RFWD2 | GRCh38.p7 | 1:175987004 | GTATCATCTTCTTTT[C/T]GGTCTTTGTCGAGAA | 64326 |
rs749433339 | in-del | -/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176142329 | ACAATAATAAAAAAA[-/G]AAATATAAAACAAAA | 64326 |
rs749436915 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175955966 | CAATTAAAATCATAC[A/C]AACTTTTCTAGTAGA | 64326 |
rs749447868 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176013005 | CCATACCAAAATCCA[C/T]GGATGTTCATGTTTC | 64326 |
rs749453236 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175989238 | AAAAAAAAAATCTAC[C/T]ATTTAAGAAAAAGTA | 64326 |
rs749486447 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176162841 | AGTTCATCATTTAAA[A/T]TTTTTTTTAAGTTTA | 64326 |
rs749488062 | snp | C/T | 1.69456e-05 | 0.00291075 | intron-variant | RFWD2 | GRCh38.p7 | 1:176149120 | AAAAATATAACTGAG[C/T]TGAAAGTTTTCTTTA | 64326 |
rs749501963 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175952326 | ACTCGGGAGGCTGAG[A/G]TGGGAGAATCGCTTG | 64326 |
rs749503090 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176092911 | CAAAGATGCCCTTAA[C/T]AGCAAGAACAACAAA | 64326 |
rs749535678 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175990674 | TTGTTTTGAGGTGTG[C/T]TGATAATTGATGTAT | 64326 |
rs749542797 | snp | A/G | 1.65067e-05 | 0.00287282 | missense | RFWD2 | GRCh38.p7 | 1:176046232 | TAATGAATATCCACT[A/G]CATCCTGGATGACAG | 64326 |
rs749552648 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176034237 | AGTCAGCACCTCAAG[C/G]AACAAACACTAAGTA | 64326 |
rs749582289 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176183002 | TTGTATTTTATATTA[C/T]ATCTTCCTGTACAAT | 64326 |
rs749584820 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176106236 | AGGTTTCTCCATGTC[A/G]GCCAGGCTGGTCTTG | 64326 |
rs749594178 | in-del | -/AAT | | | intron-variant, downstream-variant-500B, cds-indel | RFWD2, SCARNA3 | GRCh38.p7 | 1:175968177 | GCTCGGCAAGAGAAG[-/AAT]AATATTTCCACATTC | 64326 |
rs749611111 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176069176 | AGCAACAGGGTGAGA[C/T]CTCATCTCAAGAGAA | 64326 |
rs749611667 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176052355 | ATGTATTTCCATCGT[C/T]AAGCAATGCAGGACT | 64326 |
rs749630170 | snp | C/G | 9.4594e-05 | 0.00687663 | utr-variant-5-prime, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207022 | TCGGAGGAGAGGGAC[C/G]GCGACCTCGACCCTC | 64326 |
rs749631095 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176197352 | CCAGAAGTTCGAGGA[C/T]GCAGTAAGCAGTGTG | 64326 |
rs749640353 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176101349 | TCTAGATAAGCAGCC[A/G]TTCATCTTCACTCTG | 64326 |
rs749670851 | in-del | -/AAT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176019467 | GACTCCATCTCAAAT[-/AAT]AATAATAATAATAAT | 64326 |
rs749692604 | in-del | -/AGGA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176023623 | TTGGGAGGCTGAGGC[-/AGGA]AGGAGAATTGCTTGA | 64326 |
rs749697838 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176011191 | AATAGTGCTGTCCAG[G/T]ACAGTAGTCACTAGC | 64326 |
rs749701411 | snp | C/T | 3.38221e-05 | 0.00411216 | utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175945109 | ATTGTCAGCTGCAGA[C/T]GTATTTCAGCAGGAT | 64326 |
rs749701740 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176050538 | CATTCATTACCATGA[C/T]AGTGTGCCTCAAGAG | 64326 |
rs749744377 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176066463 | TGATAAAATGGGCAA[A/C]GACTTTGCCCATTTT | 64326 |
rs749751314 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176149559 | TACTTATTCACAGAT[A/G]TGAGAATATATTTCT | 64326 |
rs749766740 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176101541 | TTTCCCAAACCTTAA[A/G]TTGGTTGGCTTAGGA | 64326 |
rs749767953 | snp | A/G | 1.67318e-05 | 0.00289234 | intron-variant | RFWD2 | GRCh38.p7 | 1:176085904 | GTCTAAAATAATAAG[A/G]AAAGACACAAAACTT | 64326 |
rs749773599 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176183683 | CATTATTCATAGCAG[C/T]CAAAAGGTAGAAGAA | 64326 |
rs749795597 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176066827 | TCTCTAAACTAGAGT[C/T]TCTCTATTAATGTTC | 64326 |
rs749799856 | snp | A/C | | | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175969490 | AGAGACACAGAGAAG[A/C]AGCTCAACAAACAGG | 64326 |
rs749805712 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176193817 | AAGGAGAGTGCTTAA[C/T]GGGTACAGAGTTTCT | 64326 |
rs749808357 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175984062 | TCTGGGAAGAAATTC[A/T]AGCTGGCTGCAGAAA | 64326 |
rs749814650 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175972803 | CTCAGGAAGCTTTTT[A/C]GCTCATTGAGAATAA | 64326 |
rs749817532 | in-del | -/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176112400 | CATGTGCCATGTTGG[-/T]GTGCTGCACCCATTC | 64326 |
rs749820946 | snp | A/C | 3.31868e-05 | 0.00407336 | missense | RFWD2 | GRCh38.p7 | 1:175989434 | CCTTTGAATACCATG[A/C]TTGGCTGTTTAGTGT | 64326 |
rs749827963 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176162232 | TACTCACTCACTTAC[C/T]GTCTCAATAAATACT | 64326 |
rs749866479 | in-del | -/AA | 1.65059e-05 | 0.00287275 | intron-variant | RFWD2 | GRCh38.p7 | 1:176116600 | ACTCATGGTATCATT[-/AA]AGCAAACAAAGATAT | 64326 |
rs749866672 | in-del | -/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176021670 | GTCTACATTAACAAT[-/G]ATAGGAAAGAACTGA | 64326 |
rs749881580 | in-del | -/AAAAAAAAAAA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176049179 | GCGAGACTCCGTCTC[-/AAAAAAAAAAA]AAAAAAAAAAAAAAG | 64326 |
rs749885355 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175979784 | TATTACCATTTAGTT[A/T]CAAGTGAGCCTATTA | 64326 |
rs749895301 | in-del | -/CAACC | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176198428 | TATTAATGAAGCCTT[-/CAACC]CTTACCAAACACAGT | 64326 |
rs749903708 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176053269 | CATTCCATGTTCAAA[C/T]AGGCCTGGAAGTAAA | 64326 |
rs749904062 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176136785 | CTTCTTTAATACAAC[A/G]GTTTGATTTTACAAT | 64326 |
rs749926406 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176183745 | ACAAAATGTAGTATA[C/T]ATATACAATGGAGTA | 64326 |
rs749927664 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176037691 | TATTAATAAAGAGAA[A/T]CTACATGATGATACG | 64326 |
rs749935145 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176102512 | ACCTAAACAAACCAT[C/T]TTGCTTCTAACCTCC | 64326 |
rs749944220 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176197009 | ACGGGTTAAATTGTA[C/T]TTCCATCCCTCGCAA | 64326 |
rs749947391 | snp | C/T | 1.64871e-05 | 0.00287111 | missense | RFWD2 | GRCh38.p7 | 1:176043226 | CAAGAGTTTAGGATC[C/T]ATCAAATTAAAGTCA | 64326 |
rs749953147 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176061378 | CACGCCTGTAATCCC[A/G]GCACTTGGGAGGCCG | 64326 |
rs749953814 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176151538 | ATCTGCTATGTGACA[G/T]GAAATATGCTTCGAG | 64326 |
rs749981566 | snp | C/T | 1.91382e-05 | 0.00309334 | intron-variant | RFWD2 | GRCh38.p7 | 1:176136588 | ACAAAAAAAAAAAAG[C/T]CTAAGCCAAACCAAA | 64326 |
rs749986742 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176156510 | GCACTTATTAGACTG[C/T]GTTTTTAAAAAGAAC | 64326 |
rs749991511 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176068634 | TAAGAGATAAAAGCA[C/T]ATTTTTTTCCAAACC | 64326 |
rs749991841 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175968865 | GCACTCAAATATTCT[C/T]TCTAAACACTTTCAA | 64326 |
rs749993542 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176052229 | CAGTACAGTAACACG[C/T]TATGTAGGTTTGCAG | 64326 |
rs749993627 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175992463 | CCTCACTCGGGAAGC[A/G]CAAGGGGTCAGGGAG | 64326 |
rs750005074 | in-del | -/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176152376 | GGAGTAATGGAACTA[-/G]GAACTGTTGCTATTT | 64326 |
rs750017782 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176021785 | AAAATCATTTAGAAC[C/T]AAGTCTGATATATTG | 64326 |
rs750024454 | in-del | -/A | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176144678 | CAAGGTGGTATTGCG[-/A]AAAAAGACCAGTGAA | 64326 |
rs750043775 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176150447 | ACCTTAGACCCATTC[C/T]TCCCAAGTGAGTTAA | 64326 |
rs750049495 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176020475 | CCTGAGGTCAGAAGT[A/T]CGAGTCCAGCCTGGC | 64326 |
rs750049974 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176045831 | TATGTGCAGGCTAGG[A/G]GAAAAATTCCTGATG | 64326 |
rs750057598 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176023060 | GTAGTGAAGGATTCC[C/T]GATTCCGTGATTACA | 64326 |
rs750064816 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176205856 | TCCAGTATAGTACAG[C/T]TACATCTGACACAGG | 64326 |
rs750125741 | snp | C/T | 1.65029e-05 | 0.00287248 | missense | RFWD2 | GRCh38.p7 | 1:175988359 | TGACCCTTGAAGGAA[C/T]GTAGGCAGTATGGTT | 64326 |
rs750139136 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176129653 | CAGCTGAAGGAGATA[C/G]AGAAGCTTCAACTAA | 64326 |
rs750145093 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176062508 | ATTGCTGAGGATTTA[C/G]AACTGGAATTTTTTA | 64326 |
rs750149306 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176190501 | ACCTTAAGCTTGCCA[A/G]AAGATAATGTATGTC | 64326 |
rs750153736 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176096510 | AGGCGGCCTCAGGGG[C/T]CTGGGCCCTGCATGG | 64326 |
rs750173287 | snp | A/C | | | intron-variant, utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175971917 | CCTCCTGATGTGGCA[A/C]TCAGGAGGGTTTGAG | 64326 |
rs750194262 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176159502 | ACACATACCCTAATG[A/C]GAGCACAAGGAGAAA | 64326 |
rs750205884 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176012941 | ACGTGATTGCATTAT[A/G]TAGTCCCTAGGTATC | 64326 |
rs750206553 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176124621 | TCATTTTATGGCTGA[C/T]AGTACTCCATTGAGT | 64326 |
rs750209386 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176205002 | AGTGCACTGAACTTC[A/G]TATGGTGCCTGGCCG | 64326 |
rs750233772 | snp | C/T | 1.64781e-05 | 0.00287033 | synonymous-codon | RFWD2 | GRCh38.p7 | 1:176081193 | GAGATCACTAGCATA[C/T]GACAATGTGGCTAAA | 64326 |
rs750237634 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176198734 | GACAAAAGATGTATG[A/C]AGAATACATAAAGAA | 64326 |
rs750239376 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176109572 | ACTTTACAATGTTAA[C/T]TGGCCACATTCTACA | 64326 |
rs750272665 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175957698 | ATTTATCCAAAAGAA[A/G]TGATGGTATATAGTC | 64326 |
rs750285231 | snp | A/G | 1.65045e-05 | 0.00287263 | stop-gained | RFWD2 | GRCh38.p7 | 1:176081279 | ACTGGCTTGCAGTTC[A/G]ACTGTCATCTATATG | 64326 |
rs750287270 | snp | G/T | 7.96866e-05 | 0.00631165 | intron-variant | RFWD2 | GRCh38.p7 | 1:175987149 | GAATAGAAAAACTCG[G/T]AATTAGGACATCACA | 64326 |
rs750289893 | in-del | -/ATTATT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176107651 | ACTAACACATTAACA[-/ATTATT]ATTATAAGTAAGATA | 64326 |
rs750299132 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176203877 | ATCAACAGTTCTCAA[A/G]GAGGGGAGAAGGACA | 64326 |
rs750313656 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176036764 | GTGTTATTTTGCTTA[A/C]TTGTAGGCCAATGTA | 64326 |
rs750324408 | snp | A/G | 3.38667e-05 | 0.00411488 | intron-variant | RFWD2 | GRCh38.p7 | 1:176162831 | ATTGCAATAAAGTTC[A/G]TCATTTAAAATTTTT | 64326 |
rs750328606 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176158304 | TTATATGGAGTACCT[C/T]TCAAACACAAAAGTA | 64326 |
rs750332011 | in-del | -/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176014529 | TCTTTAAGGCTATAT[-/G]GACATTTAAAAAATA | 64326 |
rs750333946 | in-del | -/T | 0.000124216 | 0.00787988 | intron-variant, nc-transcript-variant, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175968498 | TGTAGACAAAAGGCA[-/T]TTTTTTCATTTGTCC | 64326 |
rs750384681 | in-del | -/AAAAAAAAAA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176049182 | GAGACTCCGTCTCAA[-/AAAAAAAAAA]AAAAAAAAAAAAAGA | 64326 |
rs750384952 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176090523 | GACAAACAGGAAGGT[A/G]AACTCAGAGATGTAA | 64326 |
rs750387333 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176081295 | ACTGTCATCTATATG[-/A]AAAAAAAAAAAAAAA | 64326 |
rs750407369 | snp | C/T | 1.6554e-05 | 0.00287693 | intron-variant | RFWD2 | GRCh38.p7 | 1:176184615 | AAAAGATTATTTTAC[C/T]CAATAGAATTGTCTT | 64326 |
rs750429184 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176073472 | CAACCATCACTACTA[A/G]GTATATTAAGTTTAA | 64326 |
rs750430496 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176137726 | GTACCTTATTATTAA[C/G]TCATTTCTTTAATAA | 64326 |
rs750437919 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176048794 | TTAGTTTTAACATAT[A/G]TAATACGTTTAAACA | 64326 |
rs750442755 | in-del | -/TTAA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176053478 | TTCCTTGCCTAATTG[-/TTAA]TTATTTTAATAACTA | 64326 |
rs750456523 | in-del | -/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176012668 | CTCTATAAAGGTGTA[-/C]CATTTTTTTTTTAAC | 64326 |
rs750459532 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176168885 | AGAAAGAAAATCATA[C/T]TATCTATCTCAATGA | 64326 |
rs750461544 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175947449 | GATCTTGGCTCACCA[C/T]AACCTCCACTTCCTG | 64326 |
rs750463079 | snp | C/G/T | 3.3105e-05 | 0.00406837 | missense | RFWD2 | GRCh38.p7 | 1:176027641 | ACACATTAGCCTTTG[C/G/T]CTCAATGCTTGCCAC | 64326 |
rs750469792 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176200526 | CCACCCCAAACCACA[C/G]AGATTAGGAAAGAAG | 64326 |
rs750473139 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175964880 | TATCTGTTAATTCCT[C/T]AATATTCTCTCCATA | 64326 |
rs750504252 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175948668 | CTTCAGAAATGTGCA[C/T]CTTGTTACTAATGGC | 64326 |
rs750509122 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176155015 | TTAAAAGCATAAGAC[A/G]AATATTTACAAAAAG | 64326 |
rs750518197 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176040715 | GGGCAGTCCACTCTT[C/G]TTTGTTTCCCTTTTT | 64326 |
rs750548766 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176120060 | AAAATCCTGGATTAG[C/G]CTCCACTTTGTAGAC | 64326 |
rs750554153 | in-del | -/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176079538 | TTGTTGTGTACCTAT[-/G]CTCACTGTCTGGGTG | 64326 |
rs750562662 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176072300 | GATCCTCTCCCAGCA[A/G]GTAAAACAAATTTTC | 64326 |
rs750566068 | snp | A/C | 1.73812e-05 | 0.00294793 | intron-variant | RFWD2 | GRCh38.p7 | 1:175945199 | AAAAAGGATCCATTT[A/C]ATAAAATCATTTAAG | 64326 |
rs750588850 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176086556 | TAATATCCAGAAATT[C/G]TTAGAAAATAATTAT | 64326 |
rs750604290 | snp | C/T | | | intron-variant, utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175970717 | ATATAATTTTAAAAT[C/T]AGATACAGATATCTG | 64326 |
rs750627667 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176134851 | TGAAATCCAACGCAT[C/T]AAGGAAACAGATGGG | 64326 |
rs750632075 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176015430 | ACTTTATTAACCAAA[-/A]GTAAAGGGAAGGGGT | 64326 |
rs750637349 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176084378 | AAATGGAAGAACATT[C/T]CATGCCCATGGATAG | 64326 |
rs750639697 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175984664 | AAAAGCCACAGACAA[C/T]GCCAGCTCGTTAAAG | 64326 |
rs750646229 | snp | A/T | 1.70609e-05 | 0.00292065 | intron-variant | RFWD2 | GRCh38.p7 | 1:175989530 | GCAGAAATGGAAAGC[A/T]AAGTTAATTTTAACT | 64326 |
rs750650744 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175986884 | ATTTAATCAAACCCT[A/G]TGTATACATAATGCA | 64326 |
rs750669702 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176042136 | ATTAGCCGAGTGTGG[C/T]GGTGCACACCTATAA | 64326 |
rs750692801 | snp | A/C | 3.31466e-05 | 0.0040709 | intron-variant | RFWD2 | GRCh38.p7 | 1:176116732 | TTTACATTATTTTAA[A/C]AACAGAAAAAGTAAA | 64326 |
rs750693743 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176049685 | TCTGACATATTTAAT[C/T]ATATATATTCTCAAA | 64326 |
rs750696071 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176026983 | ATACAATGGTACAAA[C/T]GGTGTGAACTAGGAC | 64326 |
rs750698130 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176180996 | GCTTGGTAGACATAC[A/G]GTACAGGGCACAAGC | 64326 |
rs750699765 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176043166 | AGAAGGAGGTGCTGA[A/G]AAAGAGATTCAAACA | 64326 |
rs750713346 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176148540 | TGCTCGCTATAAAAC[C/T]GTTGATACAAAATTG | 64326 |
rs750732207 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176031735 | ACTAAGTGTTCTATA[A/C]AAGTTTTATTTCTTT | 64326 |
rs750770142 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176137891 | CTGAGAAGAACAGGA[C/T]CGAAAAACAACTGTA | 64326 |
rs750774750 | snp | A/G | | | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176208605 | CTTAGTAAACTACGT[A/G]CGTATTCAAGGAGGT | 64326 |
rs750782413 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176137061 | CTTTAATCATACTTT[-/A]ATAAACAAAGATTAG | 64326 |
rs750782599 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176166739 | CCAGGAGCTGGAGAC[C/T]AGCTTGGGTAACATA | 64326 |
rs750784549 | snp | C/G | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176176891 | TCTCAACTACTGTTA[C/G]AGAAAATGTTAACCA | 64326 |
rs750788368 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176141988 | GATCCTCCTACCTTC[A/G]CCAACGTGTTAGAAT | 64326 |
rs750806343 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176074180 | GATCTGCCTGCCTCG[G/T]CCCCGCAAAGTGCTG | 64326 |
rs750814603 | snp | A/G | 1.66518e-05 | 0.00288542 | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176176018 | TGTAGCTATTAGTAG[A/G]GGGGGAAAAAAAAGG | 64326 |
rs750872854 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176188385 | GAAATACCATTAATT[A/C]TTTCCAATTTTGAAG | 64326 |
rs750883481 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176094295 | AAAACTCTACAAGCA[A/T]CTAGGTTGCCTTATA | 64326 |
rs750886265 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176141490 | TGGGCAACAGAGCAA[C/G]ACTCCATCTCAAAAA | 64326 |
rs750908928 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176001446 | TACCACTACTAAAAA[C/G]AGAATGCTATGGACA | 64326 |
rs750912427 | in-del | -/TAGT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176083141 | GTGGTCTGGATATAA[-/TAGT]TAATGATTCTTTTTA | 64326 |
rs750916836 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176101086 | CTAGGGAATTCAAAG[G/T]CTACTGACAGCAGGG | 64326 |
rs750917028 | in-del | -/TACGTATATACG | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176133214 | ACGTATGTACACACA[-/TACGTATATACG]TACGTATATACGTAC | 64326 |
rs750947951 | snp | C/T | 3.58198e-05 | 0.00423186 | intron-variant, nc-transcript-variant, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175968539 | TTCCAGCAGCTTCCA[C/T]TTCTGGTGTGCTTCA | 64326 |
rs750949813 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176201721 | TCTCCTGCTACCATT[A/G]ATGCTGATGCCCCAC | 64326 |
rs750957513 | in-del | -/AGG | 1.72444e-05 | 0.0029363 | cds-indel | RFWD2 | GRCh38.p7 | 1:176206600 | TGCTTTTGTCCTCGT[-/AGG]AGTTGATGAGCCCGT | 64326 |
rs750958567 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176075018 | CTGTTTCATAAACTA[C/T]TCTTTTATTTCTTAT | 64326 |
rs750971405 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176078504 | AACTCAAGATCAATC[-/A]AAACTTAAGTCTAAG | 64326 |
rs750975623 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176140745 | TAAAGGAAAATCAAT[C/T]ACAAATTAGGAATGA | 64326 |
rs750982628 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176192315 | TTGTGTAGTTATAAG[G/T]TAGGTACAGGTGAAA | 64326 |
rs750995923 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176050148 | GGGGACATAAATTGC[A/G]TTTTTCTTTCACATT | 64326 |
rs750999740 | snp | C/T | 1.7367e-05 | 0.00294673 | intron-variant | RFWD2 | GRCh38.p7 | 1:176206530 | CCTAAGCGGCAGAAA[C/T]TCATAATTTAGGGAC | 64326 |
rs751035952 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176194615 | TGCACTCCAGCCTGG[C/T]GACAGAGCAAGACTC | 64326 |
rs751037309 | snp | A/C | 0.000266809 | 0.011547 | intron-variant | RFWD2 | GRCh38.p7 | 1:176149108 | ATTTTTCTTTTAAAA[A/C]ATATAACTGAGTTGA | 64326 |
rs751047773 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176100953 | TCTGATGGATCCAGA[A/G]GCAGATGATAACAGA | 64326 |
rs751060599 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176065080 | GCCCTGAAATAACCC[A/T]ATAAACTAATATGAG | 64326 |
rs751080736 | in-del | -/TT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176066757 | TCCTTCACCAAAAAA[-/TT]TGATAACTAGAACAG | 64326 |
rs751083621 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176161069 | GCTCCACAATATAAA[C/T]AGGGTCAGTTCTTAG | 64326 |
rs751091835 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176163359 | CTAAGCCTTTAAAAT[C/T]GAGAATCTTTCAAAG | 64326 |
rs751114043 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175977979 | TAGGGATTACCAAAA[A/G]ATAAACATTAGAAAC | 64326 |
rs751119320 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176132153 | TCTCCCCAGCTTCCA[A/G]TGTCAAGGGGTTGAG | 64326 |
rs751122265 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175991217 | TTTCACAAACCTAGA[C/T]GGTATAGACTACTAC | 64326 |
rs751133370 | in-del | -/AAAAAAAAAAAC | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176091348 | GAGACTCCGTCTCAA[-/AAAAAAAAAAAC]AAAAAAAAAAACTTC | 64326 |
rs751135882 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176113561 | TCAAAGTAGTGTTAA[C/T]ATAAATGGTAACTGT | 64326 |
rs751151643 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176127777 | TAATGGGATTGCAGG[A/G]TCGTATGGTAGTTCT | 64326 |
rs751169150 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176092688 | GTGACAATCATTTTA[A/C]AGTCCAACAATACTA | 64326 |
rs751174270 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175994670 | TACATAATGGTAAAG[A/G]AATCAATTCAACAAG | 64326 |
rs751192752 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176037474 | ATCATTTTATGAGGC[C/T]AGCATTACCCTGATA | 64326 |
rs751205637 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175979595 | ATATTAAGCCAATAA[A/T]AAACGCCTACTTTCT | 64326 |
rs751208744 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176183253 | GATATAAATCTGCCC[G/T]ATATCATATCCAACT | 64326 |
rs751209764 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176078899 | GAAAAAACACTCAGC[A/G]TCACTAATCATCAGA | 64326 |
rs751213480 | snp | C/T | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176176761 | TACAGTGAGCCATGA[C/T]TATGCCAGTGCACTC | 64326 |
rs751220341 | snp | C/T | | | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176207383 | GTCGGGGCTCCCTGG[C/T]GAAGGGAGTCTGTCT | 64326 |
rs751247735 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176108694 | TCTAGTATTATTCTA[C/T]ATTTTGCTTTTATTT | 64326 |
rs751253552 | snp | C/G | 1.72036e-05 | 0.00293283 | missense | RFWD2 | GRCh38.p7 | 1:175986948 | GAAAACTTACCCCAT[C/G]TGGTAGTGCCCTCCA | 64326 |
rs751284800 | snp | A/C | 1.64811e-05 | 0.00287059 | missense | RFWD2 | GRCh38.p7 | 1:176081163 | TTACCTAGAGACTAT[A/C]CTGGAACCATTATAG | 64326 |
rs751285390 | snp | A/G | 0.00011985 | 0.00774019 | intron-variant | RFWD2 | GRCh38.p7 | 1:175945183 | CACCTAATTGGGGGG[A/G]AAAAAGGATCCATTT | 64326 |
rs751291464 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176123245 | TAATTAAAAATTCAA[A/T]GGTTCAGGGATGTGG | 64326 |
rs751292581 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176202099 | AATTTTACCAGTGTA[C/T]CCAGTGAGAAATACA | 64326 |
rs751296759 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176170057 | TCATCTGTTTAAGTT[A/T]TATCAGGATAGTACA | 64326 |
rs751299871 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176202174 | CAGATTCTATGATAC[A/G]TTCTAGTTCACTTTT | 64326 |
rs751363973 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176082981 | TTCCATTCTAAAGAC[A/G]GCAAAAGGAATTACC | 64326 |
rs751376615 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176015181 | AAATAATGTAGGATG[A/T]ATCTAGAGAAGTTTG | 64326 |
rs751377105 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176041649 | TGAGCTACCACGCCC[A/G]GCCCCTGCTTGGATT | 64326 |
rs751377692 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176121750 | AGACAATACTAAACT[C/G]TTCTCATGGTATCTG | 64326 |
rs751381502 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176137508 | TCTAACCTGGAAATA[C/T]TGAACACATTTATAA | 64326 |
rs751391351 | snp | C/T | 0.00019757 | 0.0099371 | intron-variant | RFWD2 | GRCh38.p7 | 1:176160306 | GTTCTGGGACACGAG[C/T]GCAGAATGTGTAGGT | 64326 |
rs751446292 | in-del | -/GT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176056511 | TCATTATAATGGGGC[-/GT]GTGTGTGTGTGTGTG | 64326 |
rs751447289 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176169370 | AATTAAATAACAACA[C/T]AGGAAACATATTTAA | 64326 |
rs751448453 | snp | A/G | 1.80605e-05 | 0.00300498 | intron-variant | RFWD2 | GRCh38.p7 | 1:176046338 | TACTAAGGGGAAAAA[A/G]TATGTAATGACAACA | 64326 |
rs751468379 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176012727 | CTACATTTAGATACA[C/T]GAATACTTACCATTG | 64326 |
rs751469802 | in-del | -/A/AA | 0.0570611 | 0.159104 | intron-variant | RFWD2 | GRCh38.p7 | 1:176136574 | TAGAGAGAGAAAGAC[-/A/AA]AAAAAAAAAAAAGCC | 64326 |
rs751471490 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176136647 | TTACATTAGGAAAAT[A/G]ATTTCTATCAAACTT | 64326 |
rs751486334 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175974206 | AGTCACAGGGTTGGA[A/C]ATAAGGATGGATTCA | 64326 |
rs751493331 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176134339 | TCAAGCATAAAAATT[A/C]AAAACTCAAGATTCA | 64326 |
rs751499796 | snp | A/T | 0.00117994 | 0.0242606 | missense, utr-variant-5-prime, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176206948 | GGCTTGTCCCAGCGG[A/T]GCCCGACCCGGCCTG | 64326 |
rs751518357 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176195813 | ACCACATGTTCTCAC[C/T]TTTAAGTGGGAGCTA | 64326 |
rs751527261 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176012927 | CATCCTTGAGCAACA[C/T]GTGATTGCATTATGT | 64326 |
rs751531152 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176051892 | TGTGTTTTTAGCCAA[A/G]GGTTATTGCAAAAAA | 64326 |
rs751535455 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176182548 | AGTGCAGTCACCTAC[A/G]ACAAAGAATTATCTG | 64326 |
rs751537741 | in-del | -/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176182930 | ATACCTAATCATTCC[-/T]TTTCCTCTGATAACC | 64326 |
rs751548328 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176084202 | TCAGAATGCAGGTAT[C/T]GGGCTACTTTCAACT | 64326 |
rs751559060 | in-del | -/AGTGC | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176113028 | TGCAATTAACATGGG[-/AGTGC]AGTGCAGGTATCTCT | 64326 |
rs751567267 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176199064 | GGCTCACACCTGTAA[C/T]CCCAGCACTTTGGGA | 64326 |
rs751568367 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176061518 | TAATCCCAGCTACTC[-/A]AGGTGGCTGAGGCAG | 64326 |
rs751575071 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176180965 | AACTTGTAATGAAGC[A/G]AAATAGTAAATCAGG | 64326 |
rs751623144 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176166046 | ACCATTATATTTGAT[G/T]CTCAATAACAATACT | 64326 |
rs751623215 | snp | A/G | 1.65564e-05 | 0.00287714 | synonymous-codon | RFWD2 | GRCh38.p7 | 1:175989403 | AAACTTTGCATAAGA[A/G]ACTGCTTTACGGTGT | 64326 |
rs751642355 | snp | G/T | 0.00544955 | 0.0519141 | intron-variant | RFWD2 | GRCh38.p7 | 1:176100282 | TAATCCCAGCTACTT[G/T]GGAGGGTGAGGCAGG | 64326 |
rs751674525 | snp | C/T | 3.37149e-05 | 0.00410564 | intron-variant | RFWD2 | GRCh38.p7 | 1:175989514 | GATAAATGTAGTAAA[C/T]GCAGAAATGGAAAGC | 64326 |
rs751683472 | snp | A/G | 0.000140176 | 0.00837069 | intron-variant | RFWD2 | GRCh38.p7 | 1:176175859 | TTAGCGCTAGCACAC[A/G]ATTTTGGGGATCGAA | 64326 |
rs751687851 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176030047 | GCCTTGGACTCCTGA[A/G]TTCAAGTGATCCTCC | 64326 |
rs751700364 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176133215 | ACGTATGTACACACA[C/T]ACGTATATACGTACG | 64326 |
rs751701127 | in-del | -/GCTGGTGAGGAACTGCGTTCCTTTGGA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176007379 | CAGCTTTGTTCCGTT[-/GCTGGTGAGGAACTGCGTTCCTTTGGA]GGAAGAGAGGCACTC | 64326 |
rs751705363 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176082851 | AGAAAAATAAATAAC[A/G]TTACTTGAGGAAACT | 64326 |
rs751760960 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176146092 | AAACCAAGACTCATC[A/G]GAACGATTATATTAC | 64326 |
rs751762657 | in-del | -/ACG | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176060439 | GTCCCCAAAGTTACT[-/ACG]ACATTTTGTCCTCTT | 64326 |
rs751768567 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176097760 | TGTAATTCCAGCTAC[A/G]AGGGAGGCTGAGGCG | 64326 |
rs751802017 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175952091 | TTCCCATCAGCAAGA[A/G]TGCAAGCCAGAAGAC | 64326 |
rs751810067 | snp | C/T | 1.65762e-05 | 0.00287886 | missense, utr-variant-5-prime, intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176176005 | TGATGAATACACTTG[C/T]AGCTATTAGTAGGGG | 64326 |
rs751871722 | in-del | -/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176054163 | TCAGCAAATTATTCT[-/T]TTTTTTTTTTTTTTG | 64326 |
rs751884278 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176178340 | ACTCTGTCTCTACAA[-/A]AAAAAAAAAAATAAT | 64326 |
rs751895670 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176093931 | GGGAGGCTCAGGCAG[A/G]AGAACCACTTTAACC | 64326 |
rs751931558 | snp | C/G | 1.77817e-05 | 0.0029817 | intron-variant, nc-transcript-variant, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175968518 | TTCATTTGTCCACAT[C/G]GCTGGTTCCAGCAGC | 64326 |
rs751941450 | in-del | -/AATA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176076290 | TCTTGGACCACAGTG[-/AATA]AACATAGAAATCAAT | 64326 |
rs751942756 | in-del | -/AATAC | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175949204 | AAAATGAACATGGGT[-/AATAC]AATACTCACTATTAG | 64326 |
rs751946911 | snp | A/G | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176144895 | CTAAATATGAAAGAT[A/G]AAAGAATAAAGCTTC | 64326 |
rs751952446 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176092443 | TCATTAAAAAGGTGA[A/G]ACAAGATACAAACTG | 64326 |
rs751957414 | in-del | -/TAAAA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176046104 | AGTGTCATGCAAAGG[-/TAAAA]TAATCTCATGATAAT | 64326 |
rs751963863 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176187168 | CTCACTCTGTCACCC[A/G]GGCTGGAGTGCACTG | 64326 |
rs751969374 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176140541 | CATCAGTGCAAGACA[C/T]TTTAGTACTAGTAAA | 64326 |
rs751973155 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176181603 | ATCCCAGCACTTTGG[A/G]AGGCCGAGGCGGGCG | 64326 |
rs751983566 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176106794 | CTGCATGAATTACTT[C/T]ATCGCAATTCCTCTG | 64326 |
rs751987656 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175953588 | CAAAGTGAGACCCTG[C/T]CTTAAAAAAATAAAA | 64326 |
rs752008561 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176049233 | ACCTAAATATGTCTA[C/T]TATTTCTTCTGCTGG | 64326 |
rs752010220 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176021958 | GTGTTCACATCTTTA[C/T]TATCTTTTAATTTTT | 64326 |
rs752013652 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176071952 | AAACCAAGTCGAGAT[G/T]AGAAGAAGAAAATTT | 64326 |
rs752022672 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175986875 | TATTTTAAAATTTAA[A/T]CAAACCCTGTGTATA | 64326 |
rs752044401 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176200286 | TCAGTACAACACATT[C/T]CATCTTCACTTGAGT | 64326 |
rs752051648 | snp | A/C/T | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176186472 | CTTGAGCACAGCAGG[A/C/T]GAAGCTGCAGTGAAC | 64326 |
rs752070641 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176118098 | TTTGAATTTTACCCA[C/T]AGAAGTGAATAACCT | 64326 |
rs752090313 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176119945 | CTGGGAAATAGCAGA[C/G]TTATTATTCAAACCC | 64326 |
rs752091112 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175953831 | CTGACAAAACTAAAT[A/T]GAATAAATTGACTCA | 64326 |
rs752101428 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175974441 | GAATTTCTATAGCAA[C/G]TCCAAAAATTACAGG | 64326 |
rs752104996 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176065054 | TTATAGAAGTTGTAC[A/G]TAAGTCAATAGCCCT | 64326 |
rs752133865 | snp | C/G | 1.69723e-05 | 0.00291305 | synonymous-codon | RFWD2 | GRCh38.p7 | 1:176046309 | AAAATAGTCACAATC[C/G]CGGTCAAATTCAATA | 64326 |
rs752134478 | snp | A/G | 1.65211e-05 | 0.00287407 | intron-variant | RFWD2 | GRCh38.p7 | 1:176043689 | TGATTCATATAACAT[A/G]TAACTAGTACCCTTA | 64326 |
rs752137741 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176134573 | AAACTAACAGATCTG[C/T]CTACTGCCCTCATTT | 64326 |
rs752144895 | snp | A/C | 3.62601e-05 | 0.00425779 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175968567 | TCATTATTAAGAAGA[A/C]TTTTGTTAACCAGTC | 64326 |
rs752171471 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176011555 | GAGTATGCTTATCAT[A/G]CCATCTTAACAATCA | 64326 |
rs752187933 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176070747 | ACCTTGAGCTCCTGG[A/G]CTCAAGAGATCCTTC | 64326 |
rs752190221 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176160630 | TATGAACAGACACTT[A/C]TCAAAAGAAGACATT | 64326 |
rs752190697 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176112651 | TATCAAATGCTACAA[C/T]TCATTCACCTAATCT | 64326 |
rs752192737 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175976505 | CTGGTCTCAAACTCC[G/T]GGCCTCAAGTGATCC | 64326 |
rs752211048 | in-del | -/CG | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176187402 | ACACATATAAATATA[-/CG]TGTGTGTGTGTGTGT | 64326 |
rs752229314 | in-del | -/AA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176089354 | ACTGATTATCAGATT[-/AA]GAGGCAATAATATAC | 64326 |
rs752238517 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176163405 | GTTTTTGTTTGAATA[C/T]AGACAAAGTCTCGCT | 64326 |
rs752240425 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176174872 | TCTTTAGCTTATTAT[G/T]CATTCCCAAAACATT | 64326 |
rs752244980 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176039187 | AAAATAGCTGAAAAA[A/T]TCCCAAATAATTCTA | 64326 |
rs752254152 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176096939 | TTTGTGGCCCGGGGT[C/T]CGATCCTGGCTTAGG | 64326 |
rs752257593 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176012471 | AGCTTAAGTTTTAAA[A/G]TTAATGAAGTAAAAA | 64326 |
rs752262366 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176140467 | CACATATTAAATTTG[A/T]GGTGTTTCCATTTTA | 64326 |
rs752269707 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176100442 | TTATATTTCAAGACT[C/T]ATCATATATTTGTCA | 64326 |
rs752276089 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176068412 | AACTCTGAGAGTGGA[A/G]CCCATCAATCTGTGT | 64326 |
rs752295040 | snp | C/T | 0.00187491 | 0.0305605 | intron-variant | RFWD2 | GRCh38.p7 | 1:176160285 | TTTTTTTTTTTTTTA[C/T]TTTAAGTTCTGGGAC | 64326 |
rs752295047 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175989725 | TGTCATGAAAAAAAT[A/G]TTAATATAAACATTA | 64326 |
rs752305281 | in-del | -/AGA | | | cds-indel, intron-variant | RFWD2 | GRCh38.p7 | 1:176135021 | GTACCTGTGTGATGG[-/AGA]AGGAGCTTCAAATTG | 64326 |
rs752317850 | snp | A/C | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176186160 | CAATCAATTCACTGA[A/C]TATGTCAGGAGCTAT | 64326 |
rs752352313 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176154580 | CAAGTGAGAACTAAA[C/T]GATGAGGACACATGG | 64326 |
rs752370212 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176124934 | ACTAGCATTTGTTAC[C/T]GCCAAACTTTTGGAT | 64326 |
rs752385340 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176086571 | GTTAGAAAATAATTA[C/T]CAAATAGAAAATGAG | 64326 |
rs752400080 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175945218 | AATCATTTAAGATAT[-/A]AAAAGGAATTTAATG | 64326 |
rs752400137 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175975944 | TAAGAACAGTGAGAT[C/T]TCCATAAGGGATCTT | 64326 |
rs752424140 | in-del | -/TAC | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176089368 | TAAGAGGCAATAATA[-/TAC]ACATGCCAAAGAGTT | 64326 |
rs752450592 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176134885 | TATGAATATCATTTC[C/T]AGATCATGACCAAAG | 64326 |
rs752469867 | in-del | -/T | 1.65597e-05 | 0.00287743 | intron-variant | RFWD2 | GRCh38.p7 | 1:176184606 | TAAAATGTTAAAAGA[-/T]TATTTTACTCAATAG | 64326 |
rs752472140 | in-del | -/CTCTCTCTCTCTCTC | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176099519 | TGTCTCTCTCTCTCT[-/CTCTCTCTCTCTCTC]TCTCTCTCCCTGGCT | 64326 |
rs752473287 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176100749 | CAGGCATAACTATAT[C/G]CACCAGTTATCTGGG | 64326 |
rs752476020 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176151784 | CCAACTGGGAGAAAA[C/T]ACATTGGTCATAACT | 64326 |
rs752477506 | snp | C/T | 1.68221e-05 | 0.00290014 | intron-variant | RFWD2 | GRCh38.p7 | 1:175989501 | CAAAACAAAATTAGA[C/T]AAATGTAGTAAATGC | 64326 |
rs752481335 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176055882 | TTTCTCTAATTTCTT[C/T]GCTTGGTTGTTTAAT | 64326 |
rs752503235 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175981320 | GCTTCCACTATTTCA[C/T]TGAGAAGTTGGCTGT | 64326 |
rs752511027 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175947039 | CACAGATGCAAGCTA[C/T]CTATTCTTTTCCCTT | 64326 |
rs752523984 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176194415 | GAGGCCGAGGCAGGC[A/G]GATCACAAAGTCAGG | 64326 |
rs752536161 | snp | C/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176182455 | TCTAGAGACATTTTT[C/G]GTTGTCACAACCCCA | 64326 |
rs752538197 | snp | A/G | 0.000239894 | 0.0109494 | missense, utr-variant-5-prime, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176206911 | GAGGCGGAAGTCACC[A/G]AGGAGGCCGCCGAGG | 64326 |
rs752559391 | in-del | -/AA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175974924 | CAAGACCCTGTCTCA[-/AA]AAAAAAAAAAAAAAA | 64326 |
rs752561771 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176024112 | GAAATACAAAAAATT[A/G]GCCAGATGTGGTGGC | 64326 |
rs752573628 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176084538 | AAAAAAGAGCCCACA[C/T]TGCCAAGAGAATCCT | 64326 |
rs752588035 | snp | A/G | 1.87208e-05 | 0.00305942 | intron-variant | RFWD2 | GRCh38.p7 | 1:176149086 | ATTCCTACAATAGAA[A/G]ATTATAATTTTTCTT | 64326 |
rs752591366 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175982450 | TCTCAGCCTACTCCA[C/T]GTGAAGATGAGGATG | 64326 |
rs752592554 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176148878 | AACAAATCTTAAGGA[A/G]ACCTCCTAAAAATTC | 64326 |
rs752599512 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176089541 | CCAACAACTGTACCA[C/T]AATGCCAAATGCATA | 64326 |
rs752599552 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175962062 | TTTATCTGTGAATTT[C/T]ATTTATGGATAACAA | 64326 |
rs752601452 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176049995 | CTACTGCTATACAAC[A/G]TTCATTTCTGCCATC | 64326 |
rs752610141 | snp | A/G | | | upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176208040 | TCAGTCGGAACCTAG[A/G]TTTATTGTGGATCTG | 64326 |
rs752616410 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176204174 | GTTCTCATTTTGTCC[C/T]TACCTGTCCAACGAC | 64326 |
rs752627013 | in-del | -/ATG | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176015920 | AAATTCTTCTGTAAT[-/ATG]ATTTTTTTAAAAAGA | 64326 |
rs752627968 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176181118 | AGGCTACAGATACAG[A/G]TAACAGTGGGTTCTC | 64326 |
rs752663217 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176097540 | TGTGTTGTGTGTGTG[A/G]TGTCTATAAAAAAGC | 64326 |
rs752663821 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176099330 | TCAAGCAAAATAAGA[A/G]TTAACTAAATGAACT | 64326 |
rs752670599 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176113528 | CTGGTTTCTAGCTCA[C/T]AGGATTTGCTAGAAA | 64326 |
rs752673836 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175947828 | TCAATGGAAGAAAAG[A/C]CAAAAGAAACAAAGA | 64326 |
rs752688141 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176066424 | CCTAAATAGTAAAGT[A/G]AACTCCTACTAAACT | 64326 |
rs752696054 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176030017 | AGTGCACTGGTATGA[C/T]CATAGCTCACTGCAG | 64326 |
rs752699432 | snp | A/G | 1.85696e-05 | 0.00304704 | missense, utr-variant-5-prime, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176206731 | CGGGACAGGCCCGTG[A/G]ACACCGCCCCGCCGC | 64326 |
rs752712211 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176191492 | TTCCTCTTTTCCCTT[A/C]ATTTCTTAATTCTTC | 64326 |
rs752720770 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176161663 | ATACCTGCTTTACTG[A/T]TTTAGTTCACAAACA | 64326 |
rs752755415 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175974072 | CTTATTCTGTAACCA[C/T]TGGGGAAACACTAAC | 64326 |
rs752766418 | snp | A/G | 0.000103751 | 0.0072017 | intron-variant | RFWD2 | GRCh38.p7 | 1:176168720 | TTCAAAACCAAGGGA[A/G]GCAGAGAGGAGCAGA | 64326 |
rs752772331 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176178573 | AAGATAAGAGATGGC[C/T]GGGAGCAGTGGCTCA | 64326 |
rs752835819 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176062249 | CCTTGTGATCTGCCC[A/G]CCTCAGTCTCCCAAT | 64326 |
rs752838546 | snp | A/G | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176144991 | CAAAACACACTAAGT[A/G]TAACAGATAAGATAA | 64326 |
rs752856887 | snp | C/T | | | intron-variant, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176145251 | ATGTAGTACTAGGTG[C/T]TCAACCTCATAAGTC | 64326 |
rs752870248 | snp | A/G | 1.66112e-05 | 0.00288189 | synonymous-codon | RFWD2 | GRCh38.p7 | 1:175988403 | CAGTTTTAGCTGACT[A/G]TCTGTTGAGCTGAGG | 64326 |
rs752873696 | in-del | -/TC | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176017437 | TCCCTGCTAGGTTTT[-/TC]TTAGGCGGGAAATAA | 64326 |
rs752884277 | in-del | -/TAA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175982527 | CTTTTATGATTTTCT[-/TAA]TAATATTTTCTTTTG | 64326 |
rs752916937 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176131371 | AGTAGGTAGAATATA[A/T]AGTTCTGTGGGGGGC | 64326 |
rs752920334 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176033462 | TATTAAGGAAATCTG[A/G]AATGAAGAAGAACCT | 64326 |
rs752923728 | snp | C/T | 1.76914e-05 | 0.00297412 | intron-variant | RFWD2 | GRCh38.p7 | 1:176163805 | AATAGTAATAAGAGT[C/T]GAAACATACGGTGCT | 64326 |
rs752928258 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176143685 | CAAGTAGGGGGACCA[A/G]TTGTCCTGGTGGGGT | 64326 |
rs752943112 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175966194 | AAGGTCTTGGTCTTT[A/C]AACTAAAATGTTAGT | 64326 |
rs752945811 | in-del | -/ACACATACGTATATACGTACATATATATACGTATGTAC | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176133134 | ACTATATATACCCAT[lengthTooLong]ACACATACGTATATA | 64326 |
rs752972143 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176009533 | AGTAGCTAAAAATTG[A/C]GTACTGCACGAAGGT | 64326 |
rs752985120 | in-del | -/TATCTGC | 0.000203355 | 0.0100815 | intron-variant | RFWD2 | GRCh38.p7 | 1:176160223 | CTTTCACTATGTAAT[-/TATCTGC]TTTTGGTATGGTAGC | 64326 |
rs752999054 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176203641 | TGTATCCAATGTCAA[A/G]CTAAATACTACTGTC | 64326 |
rs753018427 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176158127 | ACTGCAAGGCACATC[A/T]TAATCAAAACACTTA | 64326 |
rs753033380 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175950606 | CAGGTTATTTTTTAC[C/T]TGCTAAATAAAATAA | 64326 |
rs753070213 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176054887 | GTTTTCCATAACCTC[G/T]CCTCTCGTTCTCTTT | 64326 |
rs753079472 | snp | A/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176021557 | GACATAATTTTTTAA[A/T]CATTAAAAATACATT | 64326 |
rs753083990 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176199027 | TTGCTGGTAGAAATG[C/T]AAAATGGTGGCCGGG | 64326 |
rs753089499 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176103943 | ATACTAAAGTTCCTA[C/T]GAAAAAACAAACAGG | 64326 |
rs753096068 | snp | C/T | 1.6483e-05 | 0.00287076 | synonymous-codon | RFWD2 | GRCh38.p7 | 1:176043190 | TCAAACAGTACCTTT[C/T]GCATCATCAGAACCT | 64326 |
rs753102697 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176050214 | TCAACAGCTGAAATA[C/T]GTAATTCAGCTGTAG | 64326 |
rs753116959 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175983878 | TCTGTGGAACTCTGT[A/C]CTTGAGAGAGATGAG | 64326 |
rs753123266 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176116438 | TTTAAGTTCTTATCA[C/T]TGAAAAAGCAAATAT | 64326 |
rs753137653 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176117970 | ATAAAATTTAAGCAA[C/T]TGAGATTACTAATTA | 64326 |
rs753153355 | snp | A/T | 3.3054e-05 | 0.00406521 | intron-variant | RFWD2 | GRCh38.p7 | 1:175947266 | CAAGAGCTTTTAAAG[A/T]ATAGAGAAGGATTTC | 64326 |
rs753157856 | in-del | -/CAA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176117516 | TACATAAAAAACTAT[-/CAA]CAACTGAAAATCACA | 64326 |
rs753162838 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176165782 | CACAGGGATTAAGAA[A/C]TAAGCCTGGAAATGT | 64326 |
rs753195174 | snp | A/C/G/T | 0.000156163 | 0.00883533 | synonymous-codon, utr-variant-5-prime | RFWD2 | GRCh38.p7 | 1:176206625 | GAGCCCGTTGCAGAG[A/C/G/T]GGGGCGAGGAGAGGT | 64326 |
rs753197621 | in-del | -/A | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176151359 | AAGAAAGAAAAAGAA[-/A]AGAAAGAAAGAAAGA | 64326 |
rs753232363 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176044280 | AAAAGTCTTGACTTG[A/C]CTAATTATAACTTAT | 64326 |
rs753239748 | snp | A/C | | | intron-variant, utr-variant-3-prime | RFWD2 | GRCh38.p7 | 1:175967608 | AACAGCAAAACACAC[A/C]ACAGGAAAAACCAAG | 64326 |
rs753248337 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175985698 | TAATTCTTTCCTGTC[C/T]TGTTTGCTTTCCAAT | 64326 |
rs753250651 | snp | A/C | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176179389 | CTTTTCTTTAAAATA[A/C]ATGATAGAAAATGTG | 64326 |
rs753252247 | snp | A/G | 3.38238e-05 | 0.00411227 | intron-variant | RFWD2 | GRCh38.p7 | 1:176135092 | CACTCATTTCCTGAA[A/G]ATAAAATTATTTGAA | 64326 |
rs753257650 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176069099 | CTGAGGTGGGAGGAT[C/T]ACTTGAGCCTAGGAG | 64326 |
rs753260417 | in-del | -/AA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176053226 | CCCAGCTCTCCCCTG[-/AA]TATACTGCTTCCTCA | 64326 |
rs753274731 | snp | C/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176028596 | AAAAATCAATATAGA[C/T]AAACGATAAATTTAT | 64326 |
rs753278498 | snp | C/T | 3.49638e-05 | 0.00418099 | intron-variant | RFWD2 | GRCh38.p7 | 1:176149081 | ATGTGATTCCTACAA[C/T]AGAAAATTATAATTT | 64326 |
rs753296915 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176123702 | AACTTTACAGAGTAG[A/G]GTAAAAGAATTAAAA | 64326 |
rs753318692 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176023362 | TACAGGAATTATAAA[G/T]GAATGTTATTAACAA | 64326 |
rs753328068 | in-del | -/AGGGA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176168511 | AGAAGGAAGGGAGGG[-/AGGGA]GGGAGGGAGGGGAAA | 64326 |
rs753335208 | snp | C/T | 3.29609e-05 | 0.00405948 | synonymous-codon | RFWD2 | GRCh38.p7 | 1:176043749 | TGTGAATCCATCCCA[C/T]AAAATAACAGTGCCT | 64326 |
rs753336400 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176091951 | GAAAGAATACTAACT[A/G]AAAGAGAAAAAATAG | 64326 |
rs753345347 | in-del | -/AA | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176141695 | ATGGCAGACCTGATT[-/AA]AAGACTTCATTTAAC | 64326 |
rs753348880 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176076152 | AGAGTACTACACCCA[A/G]CAACCACAGAATATA | 64326 |
rs753375414 | in-del | -/A | 1.65222e-05 | 0.00287417 | intron-variant | RFWD2 | GRCh38.p7 | 1:175947261 | AGAACAAGAGCTTTT[-/A]AAAGTATAGAGAAGG | 64326 |
rs753390202 | snp | C/T | 0.000100691 | 0.00709476 | intron-variant | RFWD2 | GRCh38.p7 | 1:176046136 | AATTACATATGCAAA[C/T]TGTTACATCTATACT | 64326 |
rs753390281 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175952283 | AAAAATTAGCTGGGC[A/G]TGGTGGCAGGAGCCT | 64326 |
rs753403666 | snp | G/T | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176114360 | ACAGGATGATGTACA[G/T]AGTAGTCACATAAAC | 64326 |
rs753412192 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175953587 | ACAAAGTGAGACCCT[A/G]TCTTAAAAAAATAAA | 64326 |
rs753417545 | in-del | -/TTTTTTTT | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175972462 | TACAAAATACAAGAA[-/TTTTTTTT]TTTTTTTTTTTTTTG | 64326 |
rs753428402 | snp | A/C | | | intron-variant, upstream-variant-2KB, utr-variant-3-prime | RFWD2, SCARNA3 | GRCh38.p7 | 1:175968735 | GTGAAGAACATACAC[A/C]AGGGAAGAAGGATTT | 64326 |
rs753438002 | snp | C/T | 0.00134741 | 0.0259208 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176206856 | CGCTGCCGCCGAAAC[C/T]GCCACGGAAGGCGGC | 64326 |
rs753448415 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:176009543 | AATTGCGTACTGCAC[A/G]AAGGTTTTTACAGTG | 64326 |
rs753480291 | snp | A/G | | | intron-variant | RFWD2 | GRCh38.p7 | 1:175953648 | GATAAGATACACCAC[A/G]CAAACATTAATCGTA | 64326 |
rs753481346 | snp | A/G | 2.83837e-05 | 0.0037671 | missense, utr-variant-5-prime, upstream-variant-2KB | RFWD2 | GRCh38.p7 | 1:176206717 | CCGCGCAGCTGTGCC[A/G]GGACAGGCCCGTGGA | 64326 |
rs753496715 | snp | C/T | 1.6836e-05 | 0.00290133 | intron-variant | RFWD2 | GRCh38.p7 | 1:176148965 | GGGAACAGTTAACAA[C/T]AGTAAATAAAACATT | 64326 |