SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs141620630 | snp | C/T | 0.0581099 | 0.160244 | intron-variant | FBXO42 | GRCh38.p7 | 1:16285529 | TGCCTGCCTTGGCCT[C/T]CCAAAGTACTGGGAT | 54455 |
rs141662033 | in-del | -/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16281472 | TCTTTTTCTTTTTTT[-/G]TTTTTTTTTTTTTTT | 54455 |
rs141749221 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | FBXO42 | GRCh38.p7 | 1:16284830 | AAAATTAGCTGGGTG[A/T]GGTGGTACATGCCTG | 54455 |
rs141862662 | in-del | -/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16304131 | TTTTTTTTTTTTTTT[-/T]CTGAGATGGAGTTTC | 54455 |
rs141868297 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16340799 | AAGCAGGAGTAGATA[C/T]TATAGAACAACTGAA | 54455 |
rs141891238 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | FBXO42 | GRCh38.p7 | 1:16280644 | AAATAAAACACTATG[C/T]TAGCACCTGAAGTCC | 54455 |
rs141906074 | snp | A/T | 0.0486741 | 0.148216 | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16316623 | GCCTGTAATCCCAGC[A/T]ACTCAGGAGGCTGAG | 54455 |
rs141913303 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16312001 | ATGGGTAAACAAACT[A/G]TGGTGCATCTAGACA | 54455 |
rs141939025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16329539 | CAGTGAGCCAAGATC[A/G]CACCACTGCACTCCA | 54455 |
rs141947500 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | FBXO42 | GRCh38.p7 | 1:16262857 | TGGGACTACAGGCAC[A/G]TGCCACCACGGCAGG | 54455 |
rs141955332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16297080 | AGTAGGTGTAACTGG[A/G]ATTACAAGCACACAC | 54455 |
rs142031548 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16306746 | GCTCTGCTACCCAGG[A/C]TGCAGTGGCATGCAT | 54455 |
rs142090945 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | FBXO42 | GRCh38.p7 | 1:16315663 | TCTCTTCACTGAAAA[C/G]CAGAGTGGCAGCCAA | 54455 |
rs142160335 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16328159 | CATCAAAGAGTGAAA[C/T]TTAATACATGTAAAT | 54455 |
rs142167243 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FBXO42 | GRCh38.p7 | 1:16252634 | TTGTGCTTGTGACCC[A/G]TGAATCAACTGAGTG | 54455 |
rs142177471 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FBXO42 | GRCh38.p7 | 1:16264327 | GAATAGCTGATATTC[A/G]ATAGTTAAAAAGGCA | 54455 |
rs142197327 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | FBXO42 | GRCh38.p7 | 1:16308692 | TTGTTTGTTTGTTTC[A/G]TAGAGATGGAGGTTG | 54455 |
rs142264882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16260975 | ACCTCCCAAAGTGCT[A/G]GAATTACAGGCATGA | 54455 |
rs142445143 | snp | A/G | 4.94222e-05 | 0.00497078 | missense, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16305851 | GATAAGGATAGGTAC[A/G]GCTCTCCCACTGAAT | 54455 |
rs142541756 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | FBXO42 | GRCh38.p7 | 1:16275066 | AATTCATTATATGAG[A/G]TCTTTAAGAACCCAT | 54455 |
rs142587211 | snp | C/G | 0.0322114 | 0.122752 | intron-variant | FBXO42 | GRCh38.p7 | 1:16320339 | GCACTCTAGCCTGGG[C/G]AACAAGAGCAAACTC | 54455 |
rs142625537 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16317658 | GGCAGGCACAGTGGC[A/T]CATGCCTATAATCCC | 54455 |
rs142631767 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | FBXO42 | GRCh38.p7 | 1:16333009 | CCTTTCTCATTTCTA[C/G]TCTCTGCTCTTGCTG | 54455 |
rs142645975 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16344058 | GCTGGAGTGCAATGG[C/T]GCAATCTTGGCTCAC | 54455 |
rs142652447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16269486 | CCTCAGCTTCCTGAG[C/T]AGCTGAAATTATACA | 54455 |
rs142663265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16351342 | TTCTCAAAAAGGAAC[A/G]ACATAGTTTCAACGT | 54455 |
rs142668900 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16277204 | TGTCCTCTTGTTATA[C/T]TGTCTGATATTCAGC | 54455 |
rs142710621 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | FBXO42 | GRCh38.p7 | 1:16290634 | GAGGCAGAGGTTGCA[A/G]TGAACCAAGATCGCA | 54455 |
rs142730122 | snp | C/T | 0.021333 | 0.101051 | intron-variant | FBXO42 | GRCh38.p7 | 1:16286598 | GGACACAGGGCCAAA[C/T]TATATTACTAACTAA | 54455 |
rs142797369 | in-del | -/T | 0.0573587 | 0.15934 | intron-variant | FBXO42 | GRCh38.p7 | 1:16266011 | TTACACACTTCAGAC[-/T]TTTTGGGGAGAAACT | 54455 |
rs142801842 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FBXO42 | GRCh38.p7 | 1:16343571 | AAAATCAAAAAAATT[C/T]CCAGCACTTTGGGAG | 54455 |
rs142813414 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | FBXO42 | GRCh38.p7 | 1:16301484 | ACTGGGCAATAGGGC[A/G]AAACCCCGTCTCTAC | 54455 |
rs142858259 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16265392 | TACCGTGCCCGGCCT[-/A]AAAAATATTTTTATA | 54455 |
rs142977548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16339275 | TCTATACCATTACTT[A/G]TCGACACAATGTCAC | 54455 |
rs143017709 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | FBXO42 | GRCh38.p7 | 1:16336286 | GGTCTATTCCTCTCT[A/C]CTTCAGCCAAATGAT | 54455 |
rs143020340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16308013 | AACAAAGTCAGAAGA[C/T]TGATACCACCTGACT | 54455 |
rs143024150 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16256322 | CAAAGCTGAAGAGCT[A/C/T]GCTGTTCTTCAACTG | 54455 |
rs143069546 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FBXO42 | GRCh38.p7 | 1:16348615 | CTGAGGCAGGAGAAT[C/T]GCTGGAACCCGGGAG | 54455 |
rs143106113 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16258753 | ATTTATTTATTAATC[C/T]TGAGACAGGGTCTAG | 54455 |
rs143139722 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16274619 | TTTTTTTGAGACGAA[A/G]TCTTGCTCTGTTGCC | 54455 |
rs143161132 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | FBXO42 | GRCh38.p7 | 1:16349646 | CAGGTGGATCGCCTG[C/T]GGTCAGGAGTTCAAG | 54455 |
rs143212893 | in-del | -/T | 0.404384 | 0.196635 | intron-variant | FBXO42 | GRCh38.p7 | 1:16321694 | CTGAGCTCGCAAGGG[-/T]TTTTTTTTTTTTTTT | 54455 |
rs143216428 | in-del | -/AAATGA | 0.290201 | 0.246747 | intron-variant | FBXO42 | GRCh38.p7 | 1:16324128 | TCATTTTATCAACTC[-/AAATGA]AAAAGTTATAGAAAG | 54455 |
rs143311144 | snp | C/T | 6.62515e-05 | 0.00575512 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251173 | GGGCACCTGGGGAGA[C/T]GGCCCCTGCAAGGGC | 54455 |
rs143358826 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | FBXO42 | GRCh38.p7 | 1:16265702 | CTGAGTAATCAAGAA[A/G]TCCAACCTAAAGGGT | 54455 |
rs143382840 | snp | C/G | 0.00318978 | 0.0398085 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16249903 | AAATATGTTTTTTGG[C/G]AACTTGCCACCAAAT | 54455 |
rs143440560 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16325621 | AAAAATGGAAAAATA[A/G]AGTATTCCACAAACT | 54455 |
rs143462250 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16338775 | TAACAAGATGCTGTG[A/G]TGGAATGGAACATTT | 54455 |
rs143478766 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16321507 | AGAAGTCCTTCTCAC[C/T]CTTCACATTTGTGTT | 54455 |
rs143546967 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | FBXO42 | GRCh38.p7 | 1:16294042 | TAGTCCTAAGACTGA[C/G]TCCTAATACTAAAAA | 54455 |
rs143563049 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | FBXO42 | GRCh38.p7 | 1:16297335 | TCAGAAAACTGAGCA[A/C]GTTAAGAGGTAATGA | 54455 |
rs143604088 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16308279 | AGCCACTGTGTCCAG[C/G]CTTTACTGATCTTTG | 54455 |
rs143606912 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | FBXO42 | GRCh38.p7 | 1:16293240 | ATTCTCCTGCCTCAG[A/C]CTCCCAAGTAGGTGG | 54455 |
rs143692684 | snp | C/G | 0.0185938 | 0.0946107 | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16353507 | AAACTTTGGTGTCCA[C/G]AATCCCTTATCATAA | 54455 |
rs143696126 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | FBXO42 | GRCh38.p7 | 1:16278033 | GGTGATGGAGTGACA[A/C]CCTGTATCAAAAAAT | 54455 |
rs143730419 | snp | C/T | 0.000215333 | 0.010374 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251521 | TGAGGATAGGAGAGC[C/T]GTCTCCTCTGGCTGG | 54455 |
rs143780545 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | FBXO42 | GRCh38.p7 | 1:16306308 | AGGCATGAGCCACCG[C/T]GCCCAGCCTATAAGA | 54455 |
rs143798206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16272038 | TGCATGCCCATAGTC[C/T]CAGCTACTCGAGAGG | 54455 |
rs143818159 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16350744 | AGAGTGAGAAACTGC[-/A]AAAAAAAAAAAAAAA | 54455 |
rs143836259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16266955 | ACTGCTTACTCAAAA[C/T]TATTTTGATTTTACA | 54455 |
rs143848067 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16342908 | TCAGGCCATCCCCAA[C/T]GTTTCCCCTATTCAC | 54455 |
rs143852944 | in-del | -/TT | 0.374 | 0.217081 | intron-variant | FBXO42 | GRCh38.p7 | 1:16344324 | ATGGAATATATATAA[-/TT]TTTTTTTTTTTTTTT | 54455 |
rs143956176 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16296757 | ATTTGTAGGTCTAAT[C/T]CAGTTTAGCACACCA | 54455 |
rs143990231 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FBXO42 | GRCh38.p7 | 1:16325796 | ACGCCCAACTAATTT[C/T]TGTATTTTTAGTAAA | 54455 |
rs144008049 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16309166 | TCCAACTCCCAGATT[A/C]AAGCGATTCTCCTGC | 54455 |
rs144026578 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16350820 | ATAATAACCTAAACA[C/G]TTGTCATTTTAACAA | 54455 |
rs144046902 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16345978 | GCACTCCAAGACCAA[A/G]GGTGACATATCAGAA | 54455 |
rs144085406 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16308329 | GCAATGCAGAAAAGA[A/C]AGCCTTTTGCCAGGC | 54455 |
rs144128124 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FBXO42 | GRCh38.p7 | 1:16349380 | GTCTTAAATTAGTAC[C/T]TACTTCCCAAAACAC | 54455 |
rs144192275 | snp | C/T | 0.0100714 | 0.0702442 | intron-variant | FBXO42 | GRCh38.p7 | 1:16253193 | AAACCTACAAAGACA[C/T]AGGTTTCTGACTTTC | 54455 |
rs144212305 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16247632 | GTTGCTGTAAAACTC[A/G]AACATTAAAATCAAA | 54455 |
rs144299000 | in-del | -/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16313275 | TAAAAATAAAAAAAA[-/G]AAGAAAGAAAAGAAG | 54455 |
rs144331701 | snp | C/T | 1.64779e-05 | 0.00287031 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251310 | GAAGCGGGTTTCAGA[C/T]CCCAATTCAGATCTA | 54455 |
rs144354564 | in-del | -/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16269389 | CCACCGAACCCAGAC[-/T]TTTTTTTTTTTTTTA | 54455 |
rs144397459 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16259189 | TTACCTCCCCAAGGG[G/T]ATCTATCTCCTAGCC | 54455 |
rs144451540 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | FBXO42 | GRCh38.p7 | 1:16341472 | GGGAGTGGTGGTGCA[C/T]GCCTGTAATCCCAGC | 54455 |
rs144451587 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | FBXO42 | GRCh38.p7 | 1:16298118 | TAACTCCCAGCTACT[A/G]GGGAGGCTGAGGCAG | 54455 |
rs144486493 | snp | A/T | 0.02016 | 0.0983543 | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16318112 | GCTGAATACTCACGC[A/T]CTTCTCTAAAGTTTG | 54455 |
rs144489830 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | FBXO42 | GRCh38.p7 | 1:16338247 | GCCTGGACAACAGAG[C/T]GAGACTCCATCTCAA | 54455 |
rs144498505 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | FBXO42 | GRCh38.p7 | 1:16330911 | CCTGCCATTGCACTC[C/T]AGCCTGAGCAACAAG | 54455 |
rs144573420 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16268250 | CCTGAGAGTGAGCCA[A/G]ACTGAAATATGGTAA | 54455 |
rs144643739 | snp | C/T | 0.000307953 | 0.0124049 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250718 | TGTTTTTGGATAGTA[C/T]TTCACATTCTGTTTC | 54455 |
rs144647164 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | FBXO42 | GRCh38.p7 | 1:16341942 | CGTCATTGTACTCAA[G/T]CCTGGGCAACAAGAG | 54455 |
rs144698838 | in-del | -/TTTTCTTTTT/TTTTCTTTTTT/TTTTCTTTTTTTT/TTTTTTTTTTTT | 0.459914 | 0.13578 | intron-variant | FBXO42 | GRCh38.p7 | 1:16279854 | ATGGTTTTTTTTTTC[lengthTooLong]TTTTTTTTTTGAGAC | 54455 |
rs144701082 | snp | A/G | 0.0486741 | 0.148216 | intron-variant | FBXO42 | GRCh38.p7 | 1:16340022 | CTCTACTAAAAATAC[A/G]AAAAATTAGCCAGGC | 54455 |
rs144764415 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16330410 | CTACTTGGGGGCTGG[A/G]GTGGAAGGATGGCTT | 54455 |
rs144809854 | snp | A/G | 0.0486741 | 0.148216 | intron-variant | FBXO42 | GRCh38.p7 | 1:16336041 | CTCCTGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 54455 |
rs144852900 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | FBXO42 | GRCh38.p7 | 1:16326284 | TGGTCTCGAACTCCC[A/G]ACCTCAGGTGATCCA | 54455 |
rs144973784 | in-del | -/TT | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16338805 | TATTTCCATTTGTCT[-/TT]TTTTTTTTTTTTTTT | 54455 |
rs145026381 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16289408 | CAAGATTGTCTCTTT[-/A]TAAAAAAAAAAAAAA | 54455 |
rs145112212 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16302974 | GGGTGGGGACACAGA[A/G]CCAAACCATATCTGG | 54455 |
rs145124150 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | FBXO42 | GRCh38.p7 | 1:16342273 | TGGTGGCACATGCCT[A/G]TAATCCCAGCTACTC | 54455 |
rs145140958 | in-del | -/G | 0.0126979 | 0.078662 | intron-variant | FBXO42 | GRCh38.p7 | 1:16261233 | TCTCTACAAGGCTCT[-/G]GGACACACTCCACCT | 54455 |
rs145143660 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16339558 | CCTCATGATCAGCCC[A/G]CCTCAGCCATCCAAA | 54455 |
rs145209832 | snp | A/G | 0.021333 | 0.101051 | intron-variant | FBXO42 | GRCh38.p7 | 1:16260200 | CTACATCTATTATGT[A/G]CTATGCAGCTTTTTT | 54455 |
rs145250159 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | FBXO42 | GRCh38.p7 | 1:16304923 | GCGGTGAGCCAAGAT[G/T]GCACCACTGCAATCC | 54455 |
rs145263478 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FBXO42 | GRCh38.p7 | 1:16297896 | AAAAAGTCAAGTCCA[A/G]TGAATCCATGGCTCA | 54455 |
rs145318758 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16306091 | GCAGTGGCACGATCT[C/T]GGCCACTGCAACCTC | 54455 |
rs145395696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16322160 | ATATTTTATTGGTCA[A/G]AATTAATACAAATCT | 54455 |
rs145404548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16351198 | TCGCCTCAACAATTC[C/T]GCATAGCACAAGTTC | 54455 |
rs145436337 | snp | C/G | 0.00113662 | 0.0238121 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16315356 | CATTGTCCCTTCCAG[C/G]ACAGTTTCTTCCTGG | 54455 |
rs145460454 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16338995 | TCTGTATTTTTAGTA[A/G]AGATGGGGTTTCACC | 54455 |
rs145480899 | snp | A/C | 0.00263569 | 0.0362063 | intron-variant | FBXO42 | GRCh38.p7 | 1:16305935 | CTAAGACAGAAAGAG[A/C]AAACCCTTCAGTCCA | 54455 |
rs145526045 | snp | A/G | 3.30066e-05 | 0.00406229 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251402 | TCCTATTTTCAGGTC[A/G]TATCCTTCAGGAGCA | 54455 |
rs145552732 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | FBXO42 | GRCh38.p7 | 1:16282654 | GTTCAAGACCAACCT[A/G]GGCAACACAGTAAGA | 54455 |
rs145569918 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16276570 | TAGAAATGACTCAGG[C/G]ATAGTATCTTGCGTT | 54455 |
rs145592236 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | FBXO42 | GRCh38.p7 | 1:16321895 | ATCATTAGGCCAGGC[A/G]TGGTGGCTCACGCCT | 54455 |
rs145611244 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FBXO42 | GRCh38.p7 | 1:16319105 | CTAGCACTGATGAAA[A/G]GAAGAATAAGAAGGG | 54455 |
rs145616888 | in-del | -/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16281474 | TTTTCTTTTTTTGTT[-/G]TTTTTTTTTTTTTGA | 54455 |
rs145703255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16320093 | CGCCGAGCATGGTGG[C/T]TCACGCGTGTAATCC | 54455 |
rs145760062 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FBXO42 | GRCh38.p7 | 1:16319803 | GTAGTCCCAGCTACT[C/T]GGGAGGCTAAGGCAG | 54455 |
rs145772297 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | FBXO42 | GRCh38.p7 | 1:16331696 | GAGGCGGAGGTTTCA[A/G]TGAGCCGAGATCGCA | 54455 |
rs145788510 | snp | C/G | 0.0209421 | 0.100162 | intron-variant | FBXO42 | GRCh38.p7 | 1:16347345 | ACATGGTGAAACCCC[C/G]TGTCTACTAAAAATA | 54455 |
rs145789012 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16262683 | TCAGAGATTACGCGG[A/C]TCCATCAATTTTGGC | 54455 |
rs145804148 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250071 | CACAAATGTGGAATA[A/C]AATCCTTTGTTGGGT | 54455 |
rs145817333 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | FBXO42 | GRCh38.p7 | 1:16329678 | AAAAAGGCTGGGTGC[A/G]GTGGCTTATGCCTGT | 54455 |
rs145951997 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | FBXO42 | GRCh38.p7 | 1:16314745 | AAAAATCAGCCGGGC[A/G]TGGTGGCAGGCGCCT | 54455 |
rs146007677 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16279474 | GAGATATCTTGTCTA[C/T]ATCTTGTCTAGCATC | 54455 |
rs146020417 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16274144 | GCAGTACCCCATCTC[C/T]ACAAAAACTAAATTA | 54455 |
rs146032144 | snp | C/T | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16317694 | TTTAGTAAGCCAAAA[C/T]AGGAGGATCATTTGA | 54455 |
rs146073556 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | FBXO42 | GRCh38.p7 | 1:16331196 | AGGTGGGCGGATCAC[A/G]AGGTCAGGAGTTCAA | 54455 |
rs146081658 | snp | A/C | | | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251467 | TGTCCAAAGAAGAGC[A/C]ACCCACAGCTGCCGT | 54455 |
rs146096387 | snp | A/G | 6.81013e-05 | 0.0058349 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16253120 | ACCGCCACACCCTCC[A/G]AGGATTAAGATAGTT | 54455 |
rs146131268 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16300370 | ACACACAGAGCAAGC[A/C]AACAGTTCTTCACAG | 54455 |
rs146154101 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | FBXO42 | GRCh38.p7 | 1:16336641 | GGATTACAGGCATGA[A/G]CCACTGTCCCTAGCT | 54455 |
rs146170920 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | FBXO42 | GRCh38.p7 | 1:16350313 | TTACTGCATTAATTT[C/T]ATGACTCTTTATTAG | 54455 |
rs146184449 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FBXO42 | GRCh38.p7 | 1:16334029 | CTGTACCATTTCTAT[A/G]AAAATAAGTGATGAC | 54455 |
rs146246989 | in-del | -/AAAG | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16313325 | AAGAGAAAAGAAAAC[-/AAAG]AAAGAAAGAAAGAAA | 54455 |
rs146257065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16317470 | TTGGTGATGCATGTG[C/T]CTGTAATCCCAGTTA | 54455 |
rs146268566 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | FBXO42 | GRCh38.p7 | 1:16312898 | CTCCCAGGTTTGAAC[A/G]TTTCTCCTGCCTCAG | 54455 |
rs146316160 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | FBXO42 | GRCh38.p7 | 1:16297367 | AGCAGTATGTTTAGT[G/T]CCTTAAACCCCATAA | 54455 |
rs146352957 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | FBXO42 | GRCh38.p7 | 1:16277542 | CCAGCCTGGCCAACA[C/T]GGTGAAACCCTATCT | 54455 |
rs146373196 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FBXO42 | GRCh38.p7 | 1:16258275 | TTAGGGGAACAATAC[A/G]ATTTACTGAGAAGGC | 54455 |
rs146384436 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | FBXO42 | GRCh38.p7 | 1:16252678 | CCCATAATTTTATGT[G/T]TATGTATTGGGGATT | 54455 |
rs146394888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16301056 | GCGTGCGCCCACCAC[A/G]CCCAGCTAATTTTTG | 54455 |
rs146427119 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | FBXO42 | GRCh38.p7 | 1:16272071 | AAGGCAGGAGAATTG[C/T]ATGAATCTGGGAGGC | 54455 |
rs146432170 | in-del | -/A | 0.241627 | 0.24986 | intron-variant | FBXO42 | GRCh38.p7 | 1:16338260 | CATCTCAAAAAAAAA[-/A]GAGGGAGGATCGCTT | 54455 |
rs146437504 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FBXO42 | GRCh38.p7 | 1:16264881 | GATGGTGGTATAATT[A/G]CACGGCATTCTTGTT | 54455 |
rs146447869 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | FBXO42 | GRCh38.p7 | 1:16309214 | CTGGGATTACAGGCA[C/T]GCGCCACCATACCCA | 54455 |
rs146451989 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16348426 | GTAATTCGTCGGGAG[C/T]GGTGGCTGAAGCCTG | 54455 |
rs146458835 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16306185 | TGCCACCATGCCCAG[C/T]TAATTTTATTTTTAG | 54455 |
rs146518926 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | FBXO42 | GRCh38.p7 | 1:16269555 | TTTGAGACAGAGTTT[C/T]GCTCTTGTTGCCCAG | 54455 |
rs146558815 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16288998 | AGTTTCTTACTGATA[C/T]ATGCTCATCTGAGTC | 54455 |
rs146569975 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16327138 | ACACCTTAACAATAT[A/C]GGTACTTTTTTGATG | 54455 |
rs146643943 | snp | A/G/T | 0.000115574 | 0.00760099 | missense, synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251609 | TGTTCCCCAGCGGCC[A/G/T]TTAACACAAGGAGCT | 54455 |
rs146690244 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16270405 | TGGAGAAAACAATTT[A/G]ATTAGGCCTAACAAC | 54455 |
rs146700224 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | FBXO42 | GRCh38.p7 | 1:16342122 | ACTCTACAGGCCAGG[C/T]GCAGTGGCTCACGCC | 54455 |
rs146702060 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FBXO42 | GRCh38.p7 | 1:16265340 | AGGTGGTCCTCCCGT[C/T]TTGGCCCCCCAAAGT | 54455 |
rs146729250 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16270697 | AAAAAAAAAAAAAAA[A/G]AAAAGAAAAGAAAGA | 54455 |
rs146733670 | in-del | -/AGA | 0.0134861 | 0.0810011 | intron-variant | FBXO42 | GRCh38.p7 | 1:16328717 | GCATACCTAGCACCC[-/AGA]AGTTCTTTCTAATAC | 54455 |
rs146823154 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16289743 | TCCCCTAACAGCATG[A/G]GCAACATAGTGAGAC | 54455 |
rs146880094 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16247276 | CACCAGGCGTGGTTA[A/G]ATCCTCCCCACTGAC | 54455 |
rs146907760 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16351505 | TCGGGAGATTTAACA[C/G]ACAAAGCAATTGGTT | 54455 |
rs146927966 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FBXO42 | GRCh38.p7 | 1:16298790 | GCTGAGATTATAGGC[A/G]TGAGCCACCGCGCCC | 54455 |
rs146938864 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16296189 | CTTGCATTTGCCATC[C/T]TGGATTTCAGGAAGA | 54455 |
rs146986551 | snp | A/C/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251517 | CCATTGAGGATAGGA[A/C/G]AGCCGTCTCCTCTGG | 54455 |
rs146997432 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16249159 | TTCCACTGATGAGAA[A/C]TCACCAAAAATCCCT | 54455 |
rs147033446 | snp | A/C | 0.0482946 | 0.147699 | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16316648 | GCTGAGGCAGGAGAA[A/C]TGCTTGAACCTGGGA | 54455 |
rs147033745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16266387 | GCTACTCAGGAGACT[A/G]AGGCGGGAGGATGGC | 54455 |
rs147043337 | snp | C/G | 0.0322114 | 0.122752 | intron-variant | FBXO42 | GRCh38.p7 | 1:16311469 | CTCCAACATGGGTGA[C/G]AGAGCAAGATCTTGT | 54455 |
rs147075222 | snp | C/T | 9.90132e-05 | 0.00703539 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16252289 | AGCTCCCTGCTTACC[C/T]GGCAAGCTGGATGGC | 54455 |
rs147075657 | in-del | -/A | 0.0150606 | 0.0854603 | intron-variant | FBXO42 | GRCh38.p7 | 1:16332384 | TATCTATTATTCTCC[-/A]AAAAAAAATGCTTAT | 54455 |
rs147101916 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | FBXO42 | GRCh38.p7 | 1:16271824 | ATACCTGCATACCTA[G/T]CATAGTCATTGGATG | 54455 |
rs147117901 | in-del | -/AAAGAAAGAAAG | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16313325 | AAGAGAAAAGAAAAC[-/AAAGAAAGAAAG]AAAGAAAGAAAGAAA | 54455 |
rs147162419 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16325698 | GTCTGGCTTTGTCAC[A/C]TAGGCTGGAGTGCAG | 54455 |
rs147167146 | snp | A/C/T | 0.00597247 | 0.0543191 | intron-variant | FBXO42 | GRCh38.p7 | 1:16321544 | TCTCAGCTTCCCCAA[A/C/T]GTGACTGAATGAATG | 54455 |
rs147264144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16266967 | AAACTATTTTGATTT[C/T]ACAGGCAATACTTCG | 54455 |
rs147265452 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FBXO42 | GRCh38.p7 | 1:16324731 | TGAGGTGCGAGCATC[A/G]CTTGAGCCCAGGAGT | 54455 |
rs147267803 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16343335 | GATTGCTTGAAGACA[C/T]GAATTCCAGACCAGC | 54455 |
rs147278771 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16340807 | GTAGATATTATAGAA[A/C]AACTGAACCCTTATT | 54455 |
rs147333567 | in-del | -/T | | | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16353728 | TTTTTCCATTTTTTT[-/T]GTAGACACAGGGTTT | 54455 |
rs147370342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16290646 | GCAGTGAACCAAGAT[C/T]GCACCACTGCACTCC | 54455 |
rs147379584 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16286721 | TCTCAAACTCAATAC[A/G]TTTCAAGTGGAATTT | 54455 |
rs147416324 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FBXO42 | GRCh38.p7 | 1:16343605 | GAGGCAGGTACATCA[C/T]GAGGTCAGGAGTTCA | 54455 |
rs147473940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16308162 | ATTCATTTTTTTTTA[A/G]TAGAGGTGGGGTCTC | 54455 |
rs147483522 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant | FBXO42 | GRCh38.p7 | 1:16304798 | ACATGGCGAAACCCT[A/C]TCTCTACTAAAAATA | 54455 |
rs147604433 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | FBXO42 | GRCh38.p7 | 1:16337982 | GAGGGAGGATTGGCC[A/G]GGCGCGGTGGCTCAC | 54455 |
rs147627360 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16260769 | GGTGTGACTGATCAT[A/G]GCTCACTGCACTTCT | 54455 |
rs147637117 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FBXO42 | GRCh38.p7 | 1:16255592 | CACCCACCTTGGCCT[C/T]CCAAAATGCTGGGAT | 54455 |
rs147671445 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16269840 | TATTCTTTATGTTTT[C/G]TTTGTTTTTTCTGTT | 54455 |
rs147740007 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16276608 | CATTTAGAATTAGCC[C/T]CTTATAACTACATTT | 54455 |
rs147749504 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16319172 | GGTGGGGAAGGAAAC[A/G]AAGAGTAATCTCGAA | 54455 |
rs147835300 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16302450 | ATTTATGGTAGAAGG[C/G/T]AAAGGAGAATCAAGC | 54455 |
rs147844925 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | FBXO42 | GRCh38.p7 | 1:16298205 | CACCCCAGCCTGGGC[A/G]ATAGAGCAAGACTCT | 54455 |
rs147845267 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | FBXO42 | GRCh38.p7 | 1:16341545 | GTGGGGAGGCAGAGG[C/T]TGCAGTGAGCCAAGA | 54455 |
rs147855037 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FBXO42 | GRCh38.p7 | 1:16338693 | CCTATCAAATCTCTC[A/G]GGTGGCATATAAACC | 54455 |
rs147940550 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16318397 | CACTCCAGCCTGGGC[A/G]ACAGAGCAAGACTCC | 54455 |
rs147950465 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16316612 | TAGTGGCGCGTGCCT[A/G]TAATCCCAGCTACTC | 54455 |
rs147993310 | snp | A/G | 1.65111e-05 | 0.0028732 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16294901 | CATAGACTGATTAGC[A/G]TCATAATAGCATGCA | 54455 |
rs148064191 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FBXO42 | GRCh38.p7 | 1:16285342 | GCAATGGTGCAATCT[C/T]GGCTCACTGCAACCT | 54455 |
rs148118278 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FBXO42 | GRCh38.p7 | 1:16278756 | CTGGACAGTTATTTC[C/T]AGACAGTTATTTCTC | 54455 |
rs148123084 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16353940 | AAGTTTCCGGTCTTT[C/T]TGCACCGAACCAATG | 54455 |
rs148126998 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FBXO42 | GRCh38.p7 | 1:16297063 | TCTGCCTCAGTCTCC[C/T]GAGTAGGTGTAACTG | 54455 |
rs148166641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16306621 | GTGTTCAGTAAATAT[C/T]TATAGTTGGAAACTA | 54455 |
rs148183221 | in-del | -/CAAAAAA | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16337883 | AGCGAGACTCCGTCT[-/CAAAAAA]AAAAAAAAAAAAAAA | 54455 |
rs148204328 | snp | C/G | 0.0143289 | 0.0834213 | intron-variant | FBXO42 | GRCh38.p7 | 1:16256585 | TCTTCCAGATTTAAA[C/G]AGTTTATCTTTGTGA | 54455 |
rs148344180 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | FBXO42 | GRCh38.p7 | 1:16330992 | TGGGCATGGTGGCGC[A/G]TGCCTGTAGTCCCAA | 54455 |
rs148370456 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FBXO42 | GRCh38.p7 | 1:16266142 | ACCCTTTCTACCCCA[C/T]GGAAAATGGCTATTT | 54455 |
rs148374251 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | FBXO42 | GRCh38.p7 | 1:16342298 | CTACTCAGGAGGCTG[A/G]GGCAGGAGAATTGCT | 54455 |
rs148379808 | in-del | -/G/GAAAG | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16350749 | AGAAACTGCAAAAAA[-/G/GAAAG]AAAAAAAAAAAAGAA | 54455 |
rs148425971 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | FBXO42 | GRCh38.p7 | 1:16274714 | CTCCTGCCTCAGCCT[C/T]GCAAGTAGCTGGGAC | 54455 |
rs148436012 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16318247 | AGCATGGTGAAACCC[A/G]TCTCTACTAAAAACA | 54455 |
rs148458540 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16343937 | GAGCCATAATCACAC[C/T]ACACTTTAGCATGGC | 54455 |
rs148479435 | snp | A/C/G | 0.0178098 | 0.0926698 | intron-variant | FBXO42 | GRCh38.p7 | 1:16268882 | CCCAGCTACTCGGGA[A/C/G]GCTGAGACAGGAGAA | 54455 |
rs148500707 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16301370 | CAAGGTGTTGTGAAA[C/T]AGTACAAGAAGGCTG | 54455 |
rs148688138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16308423 | AGGAGTTCGAGGCTG[C/T]AGTGCACAATGATCC | 54455 |
rs148698232 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | FBXO42 | GRCh38.p7 | 1:16349495 | GCACTTTCACGAACA[C/T]TATCTTTTCTGATCC | 54455 |
rs148727866 | in-del | -/T | | | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16353552 | TCTATTGATAATAAC[-/T]TTTTTTTTTTTGAGA | 54455 |
rs148742568 | in-del | -/A | 0.407674 | 0.194008 | intron-variant | FBXO42 | GRCh38.p7 | 1:16316170 | GCAAACCTCCATCTC[-/A]AAAAAAAAAAAAAAA | 54455 |
rs148759078 | snp | A/G | 0.00238264 | 0.0344332 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251522 | GAGGATAGGAGAGCC[A/G]TCTCCTCTGGCTGGG | 54455 |
rs148810068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16322860 | ACTACTCTGAATTCA[C/T]TGGAGAAAATCCGTA | 54455 |
rs148820459 | snp | A/G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16338753 | CTGCAAAGAACATAA[A/G/T]ACATTTTAACAAGAT | 54455 |
rs148867533 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FBXO42 | GRCh38.p7 | 1:16332106 | CTGGTTATATCTCAT[C/T]AGCTTTAATAGTTAG | 54455 |
rs148930606 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | FBXO42 | GRCh38.p7 | 1:16277820 | ATGAGGCAGGAGGAT[C/T]ACTTGAGCCTAGAAG | 54455 |
rs148966283 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | FBXO42 | GRCh38.p7 | 1:16319872 | GCCGAGATTGCGCCA[C/T]TGCCCTCTAGCCTGG | 54455 |
rs148983398 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FBXO42 | GRCh38.p7 | 1:16271570 | ACATGCATGAGCCAC[C/T]GCACCTGGCCCCTAA | 54455 |
rs148986359 | snp | A/T | 0.0232847 | 0.105357 | intron-variant | FBXO42 | GRCh38.p7 | 1:16347395 | TGGTGTGCACCTGTA[A/T]TACCAGTTACTCAGG | 54455 |
rs149023515 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16303183 | AGTCAGGCTGAAAAG[C/G]CAAGCCAGGTCCTTG | 54455 |
rs149034442 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | FBXO42 | GRCh38.p7 | 1:16341917 | CGGAGGTCGCGATGA[C/G]CCAAGATCGCGTCAT | 54455 |
rs149076849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16297908 | CCAATGAATCCATGG[C/T]TCACATGTCAGATCT | 54455 |
rs149139126 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16316913 | AAATTGTGGTACATT[C/T]GCCATGAAATATAGA | 54455 |
rs149172445 | snp | A/C | 0.00914312 | 0.0669923 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16248182 | GGCCGAGACACGTGA[A/C]GTCCCACCGCACAGG | 54455 |
rs149181938 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16265605 | AGGTGAAGCTAATGC[A/G]TAATGCTTACACTGA | 54455 |
rs149233902 | snp | C/G | 0.000100249 | 0.00707915 | missense, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16255789 | TGGCCAGCCATGGGA[C/G]GTGGCCCATGGGTTG | 54455 |
rs149283009 | snp | C/T | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250882 | CTTTAATGTCCAGCA[C/T]GTACATCTGCATGGG | 54455 |
rs149292122 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FBXO42 | GRCh38.p7 | 1:16268232 | AGAAAAATCCTTGTC[A/G]GCCCTGAGAGTGAGC | 54455 |
rs149301823 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FBXO42 | GRCh38.p7 | 1:16312733 | CTCTGGTGGGGGATG[C/T]TGATAATGGGAGAGG | 54455 |
rs149334507 | snp | A/C | 0.0197687 | 0.0974348 | intron-variant | FBXO42 | GRCh38.p7 | 1:16324114 | ATATACCACGGTTAT[A/C]ATTTTATCAACTCAA | 54455 |
rs149345806 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16262883 | GCAGGCTAGTTTTTT[C/G]TAATTTTAGTAGAGA | 54455 |
rs149377707 | in-del | -/A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16345865 | AAAAAAAAAAAAAAA[-/A/G]GACACCAGGTCTTCT | 54455 |
rs149397201 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16335728 | AAACATTAGCTGGGC[A/G]TGGTCGTGGGCACCT | 54455 |
rs149494019 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | FBXO42 | GRCh38.p7 | 1:16296447 | ATGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 54455 |
rs149514707 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | FBXO42 | GRCh38.p7 | 1:16348843 | CCTATAATCAACATT[A/G]TAAGGAATAACAATT | 54455 |
rs149547426 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16290315 | ACGCCAAGGTGATGC[C/T]ATGGTGGAGATGAAG | 54455 |
rs149610541 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | FBXO42 | GRCh38.p7 | 1:16300291 | GTTTTCTGAAATGGG[C/T]TTAGTTTACGACACA | 54455 |
rs149655321 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16338831 | TTTTTTTTTTTTTGA[A/G]ACGGTGTTTCGCCCT | 54455 |
rs149665794 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16305498 | AAGGCAGGCCTATTG[C/T]TTGAGCTCAGTTCAA | 54455 |
rs149669874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16317970 | TATACGATTACAATT[A/G]TATCAAGTTCAAAAC | 54455 |
rs149733460 | in-del | -/CAACAAC | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16343967 | CAAAAAAAAAAAAAA[-/CAACAAC]AAAAAAAGAAAACTG | 54455 |
rs149734441 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16261643 | ATGAGGTGGCAGAGA[A/T]CAACATACAGCTTTT | 54455 |
rs149765327 | in-del | -/AAG | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16270709 | AAGAAAAGAAAAGAA[-/AAG]AGAAGAAAAGATAAA | 54455 |
rs149787956 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16254765 | TACCGCTGAATCAGA[C/G]AGTGATACAGATGGA | 54455 |
rs149830026 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | FBXO42 | GRCh38.p7 | 1:16288247 | CCATTCTGGCCAACA[C/T]GGTGAAACCCCATCT | 54455 |
rs149839834 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FBXO42 | GRCh38.p7 | 1:16326245 | TTTTTTCGCAAAGAC[A/G]GGGTTTCTCCATGTT | 54455 |
rs149876490 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | FBXO42 | GRCh38.p7 | 1:16341745 | GTAGGCCAAGGCGGG[C/T]GGATCACCTGAGGTC | 54455 |
rs149884070 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16281593 | TGTGCCTCGGACTCT[G/T]GAGTAGCTTGGACTA | 54455 |
rs149928768 | snp | C/G | 0.0391387 | 0.134304 | intron-variant | FBXO42 | GRCh38.p7 | 1:16337776 | GTAATTTCAGCTACT[C/G]GGGAGGCTGAGGCAG | 54455 |
rs150033832 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16309650 | CCTGTAATCCCAACA[A/C]TTTGGGAGGCCAAGG | 54455 |
rs150042551 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FBXO42 | GRCh38.p7 | 1:16351172 | ATTTTGGTGTGTCCA[A/G]GCAAAAGCAATCGCC | 54455 |
rs150050442 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16291912 | CCTGGCCTCAAGAGA[G/T]CCTCCTGTCTCAGCC | 54455 |
rs150153007 | snp | C/G | 0.0577344 | 0.159793 | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16354118 | TCAGCCTCCCGAGTA[C/G]CTGGGATTACAGGCG | 54455 |
rs150173770 | in-del | -/TCTC | 0.0581099 | 0.160244 | intron-variant | FBXO42 | GRCh38.p7 | 1:16287313 | GTTCTAATGTCGCCT[-/TCTC]TCTGATTCTCCTAGT | 54455 |
rs150220947 | in-del | -/TC | 0.0185938 | 0.0946107 | intron-variant | FBXO42 | GRCh38.p7 | 1:16326480 | CTTGAGTTCAGGAGT[-/TC]AAGACCAGCCTGGGC | 54455 |
rs150264690 | snp | C/T | 3.30055e-05 | 0.00406222 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251032 | GAGGGATGGGCACTG[C/T]TTCTCCACTGCTCAA | 54455 |
rs150310717 | snp | C/T | 0.021333 | 0.101051 | intron-variant | FBXO42 | GRCh38.p7 | 1:16257073 | TTGAGTATTAAATAG[C/T]ATATTCAAAGCACCT | 54455 |
rs150352056 | in-del | -/CT | 0.0352966 | 0.128072 | intron-variant | FBXO42 | GRCh38.p7 | 1:16278523 | TTGTTAGAATAGACT[-/CT]ACTGTCAGCTGCTTT | 54455 |
rs150358671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16290301 | ATGGTGAAGCCCTAA[C/T]GCCAAGGTGATGCTA | 54455 |
rs150412464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16283941 | TTGATTTAAAGTAAC[C/T]GAAAAAGGCAGTATG | 54455 |
rs150483528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16342637 | CTTTTGTTCCCCTGA[C/T]CCTTAATAGTTTCAC | 54455 |
rs150522421 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FBXO42 | GRCh38.p7 | 1:16285867 | ACACCATTCTCTTTT[C/T]TGTTTTTGTTGTTCT | 54455 |
rs150643323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16312116 | GTAATCCCAGCATTT[C/T]TGGAAGCTGAGGCAG | 54455 |
rs150651143 | in-del | -/T | 0.0558544 | 0.157504 | intron-variant | FBXO42 | GRCh38.p7 | 1:16325666 | TTCTTTTTTTTGTTG[-/T]TTTTGTTTTTGAGAG | 54455 |
rs150686021 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | FBXO42 | GRCh38.p7 | 1:16262867 | GGCACGTGCCACCAC[A/G]GCAGGCTAGTTTTTT | 54455 |
rs150730622 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FBXO42 | GRCh38.p7 | 1:16321282 | TCAGATGCAATTCCT[C/T]TGTAATTACATGCCC | 54455 |
rs150799797 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | FBXO42 | GRCh38.p7 | 1:16280731 | AGTGAGCCAACATCC[A/G]CCACTGCACTCCAGC | 54455 |
rs150826927 | in-del | -/ACAA | | | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16317613 | CAAGCAAACAAACAA[-/ACAA]ACAAACAAACAGAAG | 54455 |
rs150841569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16259993 | AGGACATTTCTATCA[C/T]TGCAGAAAGTTCTAT | 54455 |
rs150846993 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16336813 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAAAT | 54455 |
rs150854458 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FBXO42 | GRCh38.p7 | 1:16272728 | CAAGTAGGATACTTT[A/G]GGTAAAAGGACATGT | 54455 |
rs150889963 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16291661 | TGCCAGGATTGTAAG[C/T]GAGAGCCACCAAGCC | 54455 |
rs150901365 | snp | C/T | 0.0581099 | 0.160244 | intron-variant | FBXO42 | GRCh38.p7 | 1:16331026 | CTGGGGAGGCTGAGG[C/T]AGGAGAATCGCTTGA | 54455 |
rs150955955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16338789 | GATGGAATGGAACAT[C/T]TTATTTCCATTTGTC | 54455 |
rs150958158 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16275140 | TTCAATAGCAAGAAA[A/C]ATTCTGAGATTCAGC | 54455 |
rs150961313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16350960 | TACAATAGAAAAGAC[A/G]CCCAATCAGATTACA | 54455 |
rs150973622 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16295333 | TCCTCCAATTCTCCT[A/G]TTGTTTTTGTTTTCA | 54455 |
rs151049038 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FBXO42 | GRCh38.p7 | 1:16253539 | TTTCTTTGGCTTAGT[A/G]CATATTGGCATCTTA | 54455 |
rs151089732 | snp | A/G | 0.000345967 | 0.0131478 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250910 | GGGCTTGCAGTTCAT[A/G]CTCTGGTATAGGGGT | 54455 |
rs151174525 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16315882 | GGTTAAGAAATAACC[C/G]TTTTTCGACCAGGCA | 54455 |
rs151184574 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16328534 | ATGATCCTGTGATAA[A/T]GGATTAGAGTGGGAG | 54455 |
rs151206607 | snp | C/T | 0.0103295 | 0.0711199 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16249035 | CTGCAGCAGGCTTTG[C/T]GCCTGAGAAACGCTA | 54455 |
rs151218314 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | FBXO42 | GRCh38.p7 | 1:16264563 | CGACAGGACCAAATG[C/T]GCCCACATCAAGCGT | 54455 |
rs151227890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16308832 | GACTGCAACCTCCAC[C/T]TCCCAGGTTCAAATG | 54455 |
rs151321559 | in-del | -/T | | | downstream-variant-500B | FBXO42 | GRCh38.p7 | 1:16246385 | TGGGTAAATTTTTTT[-/T]TTTTTTAGAGATGGG | 54455 |
rs180775359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16260365 | AGGCGTATACTGCCA[C/T]GCCCGGCTAATTTTT | 54455 |
rs180785071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16281270 | CCCTGCCTCGGTTTC[C/T]TCATTTGTAACATGG | 54455 |
rs180905093 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16354309 | CACGGCGCCTGGCCT[C/T]TTTATGTATTTATTG | 54455 |
rs180941368 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16329359 | GAGACTGAGGCGGGT[A/G]GAGTGCCTGAACTCA | 54455 |
rs180942931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16300013 | TTATTTAAGACACCT[A/G]TAGATTGATCTGAGA | 54455 |
rs180951093 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16290444 | TGCCTGTAATCTCAG[A/C]ACTCTGGGAGGCTGA | 54455 |
rs180951764 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | FBXO42 | GRCh38.p7 | 1:16334787 | CTAAATAGAAAGTAC[A/C]TAAAGATGACTCATA | 54455 |
rs180959267 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16312263 | GCTATTCTGGTGGCT[A/G]AGGAGGGAAGATGAC | 54455 |
rs180960348 | snp | C/T | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16247664 | CAATCCACAGACAGC[C/T]GGGAGGAGAGTAAGC | 54455 |
rs180973149 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16346359 | ACGCTTGCCTTTATA[G/T]AAATTAAATGAACTA | 54455 |
rs180979588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16272508 | AAGTGATCCACCCGC[C/T]TTGGCCTCCCAAAGT | 54455 |
rs181046524 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16289040 | GATGGCCTTCTGTCT[A/C]GTCTGGTTTACTTTC | 54455 |
rs181059647 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | FBXO42 | GRCh38.p7 | 1:16270691 | AAAAAAAAAAAAAAA[A/G]AAAAAGAAAAGAAAA | 54455 |
rs181089791 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16300465 | TTTCCATGGTGTATG[C/G]AGCATTCAATAAATG | 54455 |
rs181095896 | snp | C/T | 0 | 0 | intron-variant | FBXO42 | GRCh38.p7 | 1:16320019 | CTCGCTAGAGGGAGG[C/T]CTTTCAAACAACAGA | 54455 |
rs181097057 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | FBXO42 | GRCh38.p7 | 1:16328366 | TAGTCTCTACTTGAC[A/G]AAGTTGTTTCTCACA | 54455 |
rs181111459 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16344786 | GTTGTAAATATCAAT[A/G]TAAAGTTCTGATTTC | 54455 |
rs181119130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16261356 | AGGATTATCTTAGGT[A/G]AGGGCTTTCCAAAAC | 54455 |
rs181132274 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16311045 | TAAAAAATGGGTCAA[C/T]GCCGGGCACGGTGGC | 54455 |
rs181269146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16336193 | CCTGCCTACCTCAGC[C/T]TCCCGAAGTGTTGGG | 54455 |
rs181378440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16340038 | AAAAATTAGCCAGGC[A/G]TGGTGGCAGGCGCCT | 54455 |
rs181382484 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16296066 | CAGAAGGGCTGTTAC[C/T]CAAAAACTACAAAGA | 54455 |
rs181403616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16277408 | TCCTCCCTGCCCCCA[C/T]TACTAATATATTATT | 54455 |
rs181407874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16323587 | GGATCTTTTGAGGTC[A/G]GGAGTTCGAGACCAG | 54455 |
rs181415887 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16331625 | CCCAGCCTGGTGGTG[A/G]GCACCTATAATCCCA | 54455 |
rs181416304 | snp | A/G | 1.9973e-05 | 0.00316008 | intron-variant | FBXO42 | GRCh38.p7 | 1:16255856 | GGAAGTCAAGAAGTC[A/G]GCACCACACACTTTA | 54455 |
rs181440135 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16304695 | AGCAGAGGGCTGGGC[A/G]CGGTGGCTCACACCT | 54455 |
rs181455426 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | FBXO42 | GRCh38.p7 | 1:16263760 | CCGAAAAACCAAAAA[A/C]CAAAACAAAACAAAA | 54455 |
rs181466896 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16293871 | TTATAGTTACATGGA[C/G]AATTGGTGACTATGC | 54455 |
rs181474802 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16276249 | GCCGGGCATGGTGGC[A/G]TGCACCTGTAGTCCC | 54455 |
rs181508835 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16351090 | TTCCCCCAAATTTTC[C/T]TTGCCTCTTTAAATC | 54455 |
rs181605416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16314837 | TGCAGTGAGCCGAGA[C/T]TGCGCCACTGCACTC | 54455 |
rs181608404 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | FBXO42 | GRCh38.p7 | 1:16264012 | GACGAGGTTTCACCA[A/T]GTTGGCCAGGCTGGT | 54455 |
rs181648207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16253508 | AAATAAATACCAGTA[A/G]AAAAGAATGATACAT | 54455 |
rs181730895 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FBXO42 | GRCh38.p7 | 1:16306063 | AGTCTCACTCTGTCG[C/T]CCAGGTTGGAGTGCA | 54455 |
rs181772132 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FBXO42 | GRCh38.p7 | 1:16324539 | AGACTAGGTAGAAGC[C/T]AAGTGTGGTGACTCA | 54455 |
rs181816379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16285077 | CTTGAACCTAGTTGG[C/T]GGAGGCTGCAGTGAG | 54455 |
rs181858870 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16325063 | AGCAACAAAGTGAGA[A/C]CCTGTCTCTATAAAA | 54455 |
rs181873606 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16341767 | CCTGAGGTCAGGAGT[A/T]CGAGACCAACCTGAC | 54455 |
rs181921079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16315103 | GAAAAAAACTAAATT[C/T]GGAGTCTAAAAATAA | 54455 |
rs181939280 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | FBXO42 | GRCh38.p7 | 1:16276934 | TTATTTTAGATGGTT[G/T]TAAGAAAGAATAGAA | 54455 |
rs181982244 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16328937 | TGGGAGGCTGAGGCG[G/T]GTGAATCACAAGGTC | 54455 |
rs181988358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16311318 | CCCATCTCTACAAAA[A/G]TAAATAAATAAATAC | 54455 |
rs181992662 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16345355 | TTGAACCCAGGAGGC[A/G]GAGGTTGCAGTGAGC | 54455 |
rs182003683 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16289709 | AAACAAACAAAAAGT[C/T]TCCTGTTTAAAGTAG | 54455 |
rs182015492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16272362 | CCTCCCGGGTTCAAG[C/T]GATTCTTCTGCCTCA | 54455 |
rs182028131 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16340737 | TTTACTGAGCAATAG[C/G]CTTAAAATACGGTTA | 54455 |
rs182070564 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16305248 | TAAAAATTAGCCAGG[C/T]GTGGTGGCATGCACC | 54455 |
rs182088927 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16350419 | AGACACTAAGAAAAT[C/T]GACAAATTTCTATGG | 54455 |
rs182105762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16332949 | TTTTTCCAACAGATT[C/T]CAATTCAGTCATCTG | 54455 |
rs182108285 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16317407 | GCAATAGAGTGAGAT[C/T]GTCTCAACAAACAAA | 54455 |
rs182208101 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FBXO42 | GRCh38.p7 | 1:16294257 | AAATAATCTAGTTTC[C/T]TTCTGCCAGATTTCT | 54455 |
rs182214259 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16331363 | GAGCTTGCAGTGAGC[C/T]GAGATCGTGCCACTG | 54455 |
rs182230219 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16321699 | CTCGCAAGGGTTTTT[A/T]TTTTTTTTTTAAAGA | 54455 |
rs182232651 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16254267 | TTAAAAAATAGTTAA[C/T]TGGTGACAGCAGGAA | 54455 |
rs182238250 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FBXO42 | GRCh38.p7 | 1:16337604 | AATAATAGGCCAGGC[C/T]AGGCACAGTGGCTCA | 54455 |
rs182245049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16282262 | ACAGAGTCTCACTCT[A/G]TCCCCCAGGCTGGAG | 54455 |
rs182257163 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16301632 | CGCGCCACTGCACTC[C/T]AGCCTGGGTGCTTGG | 54455 |
rs182258621 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16261889 | TTTTTTATTGTTGTA[G/T]TTTTAGTAGAGGCAG | 54455 |
rs182500254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16272916 | AATAATCCTGTTGAA[C/T]GGATGTAAAGTTCTT | 54455 |
rs182517144 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16248667 | TAGCCTTCTGGCCCA[A/G]CTTTCCCTTGTAAAT | 54455 |
rs182564349 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16247268 | TTCCTCACCACCAGG[A/C]GTGGTTAGATCCTCC | 54455 |
rs182632290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16341911 | GGGAGGCGGAGGTCG[C/T]GATGAGCCAAGATCG | 54455 |
rs182637701 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | FBXO42 | GRCh38.p7 | 1:16299313 | ACCGCACCCAGCCCA[C/T]ATTTTTCTTCTCTAT | 54455 |
rs182640293 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | FBXO42 | GRCh38.p7 | 1:16278316 | AGCCGGAGATCACGC[A/C]ATTGCACTCCAGCCT | 54455 |
rs182660517 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | FBXO42 | GRCh38.p7 | 1:16312416 | TGAAAGAAACCAATC[A/G]GAAAAGGCTGTATAC | 54455 |
rs182671408 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FBXO42 | GRCh38.p7 | 1:16291240 | CTTATAAACAACTAT[A/G]TTTTATTCAGAAGGA | 54455 |
rs182873911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16348422 | TAGTGTAATTCGTCG[A/G]GAGCGGTGGCTGAAG | 54455 |
rs182925323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16347906 | AGGCAGGAGAATGGC[A/G]TGAACCTGGGAGGTG | 54455 |
rs182939626 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16322278 | AGTATCTTTTTCTTC[C/T]GAAAAACTACTATAC | 54455 |
rs182954717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16347000 | TCCACCCACCTCAGC[C/T]TCCCACAGTGCTGGG | 54455 |
rs182977643 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | FBXO42 | GRCh38.p7 | 1:16282795 | AGACCACCCTGGCCA[A/G]CATGGTGAAACCCCG | 54455 |
rs183060078 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FBXO42 | GRCh38.p7 | 1:16351332 | ATAAAAGTTGTTCTC[A/G]AAAAGGAACAACATA | 54455 |
rs183063497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16285732 | CTCCTTTCCTGGAAA[C/T]GCTTTCCTCATATGC | 54455 |
rs183066734 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FBXO42 | GRCh38.p7 | 1:16332319 | TTCCAACAATGGGAG[A/G]CACATTGTTATTATT | 54455 |
rs183066989 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16287221 | CAACTCTGGGTCTTT[A/G]CACTGATTATTCTCT | 54455 |
rs183079709 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | FBXO42 | GRCh38.p7 | 1:16297599 | GGGCGTGGTGGCTCA[C/T]GCCAGTAATCCCAGC | 54455 |
rs183080382 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16265013 | CAGGACTACATAGAG[A/C]AGCTCAACTATTTGA | 54455 |
rs183082049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16267754 | TGGATCTCAGGATTC[A/G]GGGTATACATTATTA | 54455 |
rs183094815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16316227 | TTTTCTAAACTTTTA[C/T]GCAAGACGATTCACT | 54455 |
rs183115266 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16308415 | TTGAGCCCAGGAGTT[C/T]GAGGCTGTAGTGCAC | 54455 |
rs183236014 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FBXO42 | GRCh38.p7 | 1:16302753 | GACCTCAAGTGATCC[A/G]CCCTCCTCAGCCTCC | 54455 |
rs183270400 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16329602 | ATCAATCAATCAATC[A/C]ATCCCAAAGTACAAA | 54455 |
rs183272084 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16262435 | GATCACATGGGGTGT[G/T]GTGGCTCAAGCCTGT | 54455 |
rs183390867 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16325878 | TGATCTGCCCACCTC[A/G]GTCTCCTAGAGTGCT | 54455 |
rs183401198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16286762 | CTGCCCCTTGCCAAC[C/T]TTGATCACCCAGTCT | 54455 |
rs183424675 | snp | G/T | 0.0988009 | 0.199095 | intron-variant | FBXO42 | GRCh38.p7 | 1:16261716 | TCAATTTTTTTTTTT[G/T]GTTTTTGAGACGCGT | 54455 |
rs183482299 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | FBXO42 | GRCh38.p7 | 1:16326040 | TGTGTGTGTGTGTGT[C/G]TGTGTGTGTCTGTGT | 54455 |
rs183504940 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16330274 | GCCTGTAATCCCAGC[A/G]CTTTGAGACGCCAAG | 54455 |
rs183508090 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16291698 | ATTTTTTGAGACAGG[A/G]TCTCCCTCTTTCACT | 54455 |
rs183509325 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FBXO42 | GRCh38.p7 | 1:16312615 | ATACATTCATCCAAA[C/T]CCATAGAATGCACAA | 54455 |
rs183521344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16258096 | ACATTAACCTGACAG[C/T]AGTCGAGATGCTCCA | 54455 |
rs183688901 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16342277 | GGCACATGCCTGTAA[C/T]CCCAGCTACTCAGGA | 54455 |
rs183705811 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FBXO42 | GRCh38.p7 | 1:16309619 | AAGAAAGAATGGCCA[A/G]GCATGGTAGCTCACG | 54455 |
rs183735878 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FBXO42 | GRCh38.p7 | 1:16277657 | TTGAATCCAGGAGGC[A/G]GAGGTTGCAATGAGC | 54455 |
rs183776585 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16304247 | TCAGCCTCCCAAATA[C/G]CTGGGATTACTGGCA | 54455 |
rs183787454 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16284347 | CACTCACCAGCACCT[G/T]CAATCACATATTCCC | 54455 |
rs183826644 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | FBXO42 | GRCh38.p7 | 1:16263639 | GAGGCAGGAGAAACG[C/T]TTGAACCCGGGAGGC | 54455 |
rs183839811 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16352719 | TGTCTGGGGCAACTG[A/G]GTGGTTTTCCCGGTG | 54455 |
rs183851926 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16317109 | AACATGGTGAAACTC[C/T]GTCTCTACTAAAAAA | 54455 |
rs183866781 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16258513 | AGGCAAGCACCACCA[A/T]GCCCGACTAATTTTT | 54455 |
rs183870583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16278128 | TTGGGAGGCCGAGGC[A/G]GGCGGATCACCTGAG | 54455 |
rs183911044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16330801 | CAAAAAATTAGCTGG[A/G]CATGGTGGTGGGCAC | 54455 |
rs183920450 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | FBXO42 | GRCh38.p7 | 1:16313505 | CCATGTATTTCCACA[G/T]TGCAGGGAGCCAATC | 54455 |
rs183963058 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | FBXO42 | GRCh38.p7 | 1:16339619 | CCCAGCCATAGTTAT[A/G]TTCTTATGTAAATTT | 54455 |
rs183963543 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FBXO42 | GRCh38.p7 | 1:16293341 | GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAG | 54455 |
rs183963694 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16275670 | AGCCATAGTTCAAGA[A/G]TTCATCTCCTCAAGG | 54455 |
rs183976887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16252975 | GCTATACCCAAAAAG[C/T]ATTCCTTAAATTAAA | 54455 |
rs183999192 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | FBXO42 | GRCh38.p7 | 1:16336908 | GAGAATCACTTGAAC[C/G]CGGGAGGTGGAGGTT | 54455 |
rs184008721 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16332839 | AGCCACTGCGCCTGG[A/C]CTCGACTAATGAATA | 54455 |
rs184038568 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16273770 | TGTAGTCCCAGCTAC[C/T]TGGGAGGCTGAGGTG | 54455 |
rs184046391 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16301148 | AAGTGATCCACCTGC[C/T]TTGGCCTCCCAAAGT | 54455 |
rs184049567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16297996 | TTTGGGAGGCTGAGG[C/T]GGGTGGATCACTTGA | 54455 |
rs184095512 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16259335 | ATCATCAGTACTATG[A/G]AACAGTTAGAAAAAA | 54455 |
rs184160661 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FBXO42 | GRCh38.p7 | 1:16344074 | GCAATCTTGGCTCAC[C/T]GCAACCTCCACCTCC | 54455 |
rs184162280 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16321302 | ATTACATGCCCAACA[A/C]CAATTTGCATAGCCC | 54455 |
rs184173620 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16249652 | GCATCTTAGAATTCC[C/G]TACTGGCCCCCTAGT | 54455 |
rs184193080 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16281961 | GATCCTCGACTCCCA[A/G]AGTGCTGGGATTACA | 54455 |
rs184200954 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16269946 | CTGCAACCTCCGCCT[C/T]CCAGGCTCAAGTGAT | 54455 |
rs184206175 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16310481 | GTCTGCAGTGAGCCC[G/T]GATCACGCCACTAGA | 54455 |
rs184214709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16314841 | GTGAGCCGAGATTGC[A/G]CCACTGCACTCCAGC | 54455 |
rs184224735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16350263 | CAGTGCAACATATTA[C/T]GCCAAGAAGCATAAT | 54455 |
rs184227994 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | FBXO42 | GRCh38.p7 | 1:16331221 | GTTCAAGACCATCCT[A/G]GCTAACACGGTGAAA | 54455 |
rs184306169 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16327819 | CGATTCTCTCACCTC[A/T]GCCTCCCAAGTAGCT | 54455 |
rs184335310 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16289242 | TCTACAAAAAAAAAA[G/T]AAAGAAAAGAAAATG | 54455 |
rs184339397 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16318264 | CTCTACTAAAAACAC[A/G]AAAATTAGTTGGGTG | 54455 |
rs184349665 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16271025 | ATGCCTCACAGAGGG[A/G]GACATATGAATAAAG | 54455 |
rs184355019 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | FBXO42 | GRCh38.p7 | 1:16287808 | CAAACTCTCGGCCAG[A/G]CACAGTGGCTCATGC | 54455 |
rs184357048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16333557 | TTGCACCACTGCACT[C/T]CAGCCTGTGACAGTG | 54455 |
rs184358356 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16330680 | GGTGCGGTGGCTCAC[A/G]CCTGTAATCTCAGCA | 54455 |
rs184373882 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16292249 | CTTTGGGAATTTCAA[A/C]GCATAACCTTTTCTT | 54455 |
rs184407581 | snp | A/G | 8.24069e-05 | 0.00641846 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251702 | AGGAGTGGCACTGAT[A/G]GGTGATGGGCGAGAG | 54455 |
rs184493905 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16328449 | CGATTAAGTAAATAG[C/T]TGGCAGATGGCTAGA | 54455 |
rs184496432 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16353523 | AATCCCTTATCATAA[A/C]CCAGACATTCATTTC | 54455 |
rs184516717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16313033 | CTCTTGATCTCAGGC[A/G]ATCCGCCCACGTTGG | 54455 |
rs184516861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16274350 | AAGAAAAAAAGAACA[A/G]AACAAAGCCACAGTG | 54455 |
rs184686979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16323593 | TTTGAGGTCAGGAGT[C/T]CGAGACCAGCCTGGC | 54455 |
rs184694582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16349490 | ACAAAGCACTTTCAC[A/G]AACACTATCTTTTCT | 54455 |
rs184848379 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16343300 | TGCAATGCCAACACT[C/T]TAGGTCAAGGCAGGT | 54455 |
rs184883883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16287387 | TTCCATCCTCTAACA[C/T]ACTGTTATATATTTG | 54455 |
rs184889977 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | FBXO42 | GRCh38.p7 | 1:16259685 | GCACAAGAATTGCTT[A/G]AAACTAGGAGGTGGA | 54455 |
rs184890179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16310037 | CGTCTCTACTAAAAA[C/T]AGAAAAAATTAGCCG | 54455 |
rs184898794 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | FBXO42 | GRCh38.p7 | 1:16268866 | GGCACATGCCTGTAA[C/T]CCCAGCTACTCGGGA | 54455 |
rs185013838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16262772 | GTGCAGTGGCGTAAT[C/T]GATCTCAGCTCACTG | 54455 |
rs185022021 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16283505 | GCAAGTTTTTTTTTT[G/T]TTTTTTTTTTTTGAG | 54455 |
rs185049524 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16276514 | CATGGCACTACCAAG[A/T]GTCCTTGAAACCAAG | 54455 |
rs185053198 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16303919 | CCCGGGTAATTTTTT[A/G]TATATATATTTTTTT | 54455 |
rs185064204 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | FBXO42 | GRCh38.p7 | 1:16338877 | GTGCAGTGGCACAAT[C/T]GCGGCTCACTGCAAC | 54455 |
rs185141789 | snp | A/C | 0.00318978 | 0.0398085 | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16354485 | AATTTTTGTATTTTT[A/C]GTAAAGACGGGGTTT | 54455 |
rs185146388 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16335781 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCTGAGAG | 54455 |
rs185166306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16300121 | TCCAGTAGTAATTTC[C/T]CTTTTCACAAGTTCT | 54455 |
rs185173616 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16294110 | CTAGCAGAATACTTT[A/C]TACTCAGTGGACACT | 54455 |
rs185176574 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16281317 | ATCCTATTGAGTTGA[C/T]ATGAAGGTTAGATAA | 54455 |
rs185176747 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FBXO42 | GRCh38.p7 | 1:16253578 | CCTCCTCCCTCTCCC[A/G]TCCTAACTGAAAGAC | 54455 |
rs185182886 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16323088 | GCTGAACATTTAAAA[C/T]GCAATCAAACGTATT | 54455 |
rs185184760 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16319691 | GCTTAGGCAGGCGGA[A/T]CACGAGCTCGGGAGT | 54455 |
rs185197548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16260389 | AATTTTTTGTATTTT[A/G]GTAGAGACGGGGTTT | 54455 |
rs185208432 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FBXO42 | GRCh38.p7 | 1:16299769 | CCTGCCTCAGCCTCC[C/T]GAGTAGTTTGGACCA | 54455 |
rs185217745 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FBXO42 | GRCh38.p7 | 1:16259544 | CAAGGCAGGCAGATC[A/G]CTTAAGGTCAGGAGT | 54455 |
rs185218793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16325574 | TAGTGTGCTACCCAA[C/T]TAAGATTCCCTTAAT | 54455 |
rs185231893 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | FBXO42 | GRCh38.p7 | 1:16306906 | GGAAAGTTTGTTTTC[C/T]TTTTTTTTCTTTTTG | 54455 |
rs185242002 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | FBXO42 | GRCh38.p7 | 1:16341792 | CCTGACCAACATGGA[A/G]AAAACCCCGTCTCTA | 54455 |
rs185248913 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16285876 | TCTTTTTTGTTTTTG[C/T]TGTTCTTTTTGAGAT | 54455 |
rs185312582 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16278648 | TAAGCTTTTCCACTA[G/T]ACACATGACAGTAAG | 54455 |
rs185331229 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16254536 | GGTCACTTAAGGTCA[C/T]TGATTCACCCACAAA | 54455 |
rs185469506 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16354254 | AACTCGTGATCCACT[C/T]ACCTCGGCCTTCCAA | 54455 |
rs185486292 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FBXO42 | GRCh38.p7 | 1:16344929 | CCTGGTGAAACCCCA[C/T]CTCTACTAAAAATAC | 54455 |
rs185505118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16319226 | GATCTGAAATGTTCC[A/G]AAAAGTGACAGACCG | 54455 |
rs185513300 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16280849 | GAACACAAACTTTAG[A/G]GACAAAATCTTGGGT | 54455 |
rs185610826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16296150 | TCTCTATCCTTTGGA[A/G]ATGACGATCACATTC | 54455 |
rs185620038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16331805 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGCTGAGG | 54455 |
rs185621015 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16299987 | ACTGAACTTTACTTA[C/T]TGCCTATTTTTTATT | 54455 |
rs185626826 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16334496 | CTCCCTGGCACTTGG[A/T]GCAAAAGGCCAGTGA | 54455 |
rs185629974 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FBXO42 | GRCh38.p7 | 1:16315892 | TAACCGTTTTTCGAC[C/T]AGGCATGGTGGCTCA | 54455 |
rs185632045 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16256454 | TGAAACTGTTGGTAA[A/T]ATCTGTGAATATGTG | 54455 |
rs185640471 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FBXO42 | GRCh38.p7 | 1:16277458 | GGCTGGGCATGGTGG[C/T]TAATGCTTGTAATCC | 54455 |
rs185734136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16305646 | TGAGCCTGGGGAGGT[A/G]GAGGCTGTAGTAAGC | 54455 |
rs185736219 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FBXO42 | GRCh38.p7 | 1:16264232 | AGCACATAGGTTTAA[C/T]ACATTTTTATTAAAA | 54455 |
rs185742491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16285100 | GCAGTGAGCCGAGAT[C/T]GCACCCCTGTACTCC | 54455 |
rs185783213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16312303 | GGAGACGGAGGTTGC[A/G]GTGAGCCAAAATCGC | 54455 |
rs185805862 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FBXO42 | GRCh38.p7 | 1:16272510 | GTGATCCACCCGCCT[C/T]GGCCTCCCAAAGTGC | 54455 |
rs185904319 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16332372 | GGAAGATTAAATATA[A/T]CTATTATTCTCCAAA | 54455 |
rs185916914 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FBXO42 | GRCh38.p7 | 1:16351363 | GTTTCAACGTCGGGG[C/T]CAGCAACTGCCAGCA | 54455 |
rs185929855 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | FBXO42 | GRCh38.p7 | 1:16329450 | TTAGCCAGGCGTGGC[A/G]GTGTGCGCCTGTAGT | 54455 |
rs185946443 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16290992 | ACATCTGATGCAGCA[C/G]TATTCTCTATCAAGA | 54455 |
rs185956913 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16248027 | AAATATTTGCTTCAG[G/T]TGCTCCTGAGGGTTA | 54455 |
rs186089543 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16277139 | CAATGAGATCAATCA[C/T]TCGTTTTTAAGACAG | 54455 |
rs186139856 | snp | A/G | 0.00160504 | 0.0282833 | intron-variant | FBXO42 | GRCh38.p7 | 1:16294723 | AAAATGATCAGGTAG[A/G]GTTTCCATGCCAAGG | 54455 |
rs186144200 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | FBXO42 | GRCh38.p7 | 1:16331402 | CCTGGGCGACAGAGC[A/G]AGACTCTGTCTCAAA | 54455 |
rs186148041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16265514 | GTGCTACAAATTTTA[C/T]ATTTATTATCTAATT | 54455 |
rs186161082 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16329195 | AAAGAAAATTGATGG[A/G]ATTGTGTAAAAGGGG | 54455 |
rs186171086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16345616 | GCACTTTGGGAGGCC[A/G]AGGCAGGCGGATCAC | 54455 |
rs186173267 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FBXO42 | GRCh38.p7 | 1:16261841 | CCTGAGTAGCTGGGA[C/T]TACAGGCACCCCCCG | 54455 |
rs186190647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16289952 | TTCTATACTTCATTC[C/T]GTTTGTTTCCTTCAT | 54455 |
rs186242133 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | FBXO42 | GRCh38.p7 | 1:16350661 | CTGAGGCAGGAGAAT[C/T]GCTTAAACCCAGGGG | 54455 |
rs186302605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16284692 | AAAAAATTAGGCCAG[A/G]CGCAGGGACTCATGC | 54455 |
rs186458106 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16304836 | TAGCCAGGTGTGGTG[A/G]CACACACCAGTAGTC | 54455 |
rs186459484 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16321776 | TAGTTCACTGCAGCC[G/T]TGAACTCCTAGGCTC | 54455 |
rs186480186 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16337840 | AGTGAGTGGAGATCG[C/T]GCCACTGTACTCCAG | 54455 |
rs186480640 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | FBXO42 | GRCh38.p7 | 1:16282280 | CCCCAGGCTGGAGTG[C/G]AGTGGCGCGATCTCG | 54455 |
rs186487218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16263885 | GCACAATCTTGGCTC[A/G]CTGCAACTTCCACCT | 54455 |
rs186489547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16251961 | AGACATGGGAACAAT[C/T]GCTGCTTTGTGTGAC | 54455 |
rs186496232 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16301745 | CTGTCTATCTTCAAG[G/T]AGACGACAATCTTGT | 54455 |
rs186504713 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16262000 | TACAGGCGTGAGCCA[A/C]CGCGCCTGGCCCAGG | 54455 |
rs186582063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16316307 | CTGTGGTGTTTACCC[C/T]GAGATAACTTTGCCA | 54455 |
rs186585329 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16341133 | AAGAGGCTGAGCAGC[A/G]TATATAGTAGGAAAA | 54455 |
rs186764279 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16261638 | AACAAATGAGGTGGC[A/T]GAGATCAACATACAG | 54455 |
rs186792982 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | FBXO42 | GRCh38.p7 | 1:16297722 | AAAAAAAAAAATTAG[C/T]CGGGCGTGGTGGCAG | 54455 |
rs186803571 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16278249 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 54455 |
rs186810223 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16324743 | ATCGCTTGAGCCCAG[A/G]AGTTAGATGCTGCAG | 54455 |
rs186817183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16258800 | AGAGTGCAGTGATGC[A/G]ATCATGGCTCACTGC | 54455 |
rs186891225 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | FBXO42 | GRCh38.p7 | 1:16343778 | CAGTGAGCCCAGATC[A/G]TGCCATTGTACTTCA | 54455 |
rs186926234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16327542 | TTAGAAAGATAAATA[A/G]ATTCAGAGTTAAAGA | 54455 |
rs186931514 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16336211 | CCGAAGTGTTGGGAT[C/T]ACAGGCATGAGCCAC | 54455 |
rs186936055 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16310058 | AAATTAGCCGGGTGT[C/G]GTGGTGGATGCCTGT | 54455 |
rs186981224 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16300820 | CCCTACATCAATCTG[A/C]AAAGGACATTCTACA | 54455 |
rs187070054 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16317959 | AGAATATATACTATA[A/C]GATTACAATTATATC | 54455 |
rs187075755 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16353218 | AAACTCTGTAAGCCA[A/G]AAAAACAAAACAAAA | 54455 |
rs187078611 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | FBXO42 | GRCh38.p7 | 1:16333320 | CTTGCCTAATTAAAA[C/T]CCACATTAAGAGCCA | 54455 |
rs187094481 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16299364 | ACAGCGGGGCCCTGA[C/G]GTCCTTACCACATGT | 54455 |
rs187095937 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16259388 | CAGACTTCAGCAAAA[C/T]AGTAATGTAAACTCT | 54455 |
rs187099294 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16278409 | ATCCAGCTGTTTCAA[C/T]GTTAGCACCGACGTT | 54455 |
rs187132645 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16247361 | AGGATCACCACAAGG[A/G]CAAGGACAGACAGAC | 54455 |
rs187161087 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | FBXO42 | GRCh38.p7 | 1:16320218 | TACAAAAAACTAGCT[A/G]GGCGTGGTGGCACAT | 54455 |
rs187164755 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16281526 | CCAGGATGTAGTGCA[A/G]TGACAGAACATGGTT | 54455 |
rs187286385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16301474 | TTGAGACCAGACTGG[A/G]CAATAGGGCGAAACC | 54455 |
rs187303018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16321310 | CCCAACACCAATTTG[C/T]ATAGCCCTTCTTTTT | 54455 |
rs187337794 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16272449 | TTTTAAGTAGAGACC[A/G]GGTTTCACCATGTTA | 54455 |
rs187350505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16309799 | CCTGTAATCCGAGCA[C/T]TTTGGGAGGCCGAGG | 54455 |
rs187367651 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16287288 | CACTTCTTGTACCCA[A/T]CAAGTCCTTGTTCTA | 54455 |
rs187368597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16326134 | GATCTCGGCTCACTG[C/T]AACCTCCACCTCCTG | 54455 |
rs187377463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16267967 | AGACCACTTGATGAA[C/T]AGGGCAGCACTTATC | 54455 |
rs187443539 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16313313 | GAGAAAGAAAGAAAG[A/G]GAAAAGAAAACAAAG | 54455 |
rs187446463 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FBXO42 | GRCh38.p7 | 1:16274715 | TCCTGCCTCAGCCTC[A/G]CAAGTAGCTGGGACT | 54455 |
rs187504784 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FBXO42 | GRCh38.p7 | 1:16337138 | GGTACTCAGAGGAAA[C/T]CTCATTCAATATCTC | 54455 |
rs187591266 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16348439 | AGCGGTGGCTGAAGC[A/C]TGTAATCCCAGCACT | 54455 |
rs187627362 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FBXO42 | GRCh38.p7 | 1:16347344 | AACATGGTGAAACCC[C/T]GTGTCTACTAAAAAT | 54455 |
rs187659262 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FBXO42 | GRCh38.p7 | 1:16291365 | TAAATGAGAATCTCA[C/T]GGGACTTTTTTTTTT | 54455 |
rs187660254 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | FBXO42 | GRCh38.p7 | 1:16329777 | ACATAGTGAAACCCC[A/G]TCTCTACTAAAAATA | 54455 |
rs187664668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16312467 | ACCTTCTAGAAAAGG[C/T]AAAACTATGGAGACA | 54455 |
rs187671220 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16273307 | CACATTACTTTAGGT[A/C]ATTAGCCCCTAATAA | 54455 |
rs187681244 | snp | C/T | 0.00993419 | 0.0697739 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16249217 | TTATTTTGACATCTC[C/T]TATGCCCAGGCCATG | 54455 |
rs187697671 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16292366 | CACTCTCGCCTAGGC[A/G]TCTGGGCTTATATCT | 54455 |
rs187703241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16332843 | ACTGCGCCTGGCCTC[A/G]ACTAATGAATATTTT | 54455 |
rs187741405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16269400 | AGACTTTTTTTTTTT[C/T]TTAAGAGAGTATCAC | 54455 |
rs187752855 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | FBXO42 | GRCh38.p7 | 1:16298012 | GGGTGGATCACTTGA[C/G]GTCAGGAGTTCGAGT | 54455 |
rs187845819 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16330713 | TTGGGAGACCGAGGA[C/G]GTGAATCACCTGAGG | 54455 |
rs187891699 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16287202 | ACTATATCAAGCACA[A/C]TCCCAACTCTGGGTC | 54455 |
rs187949276 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | FBXO42 | GRCh38.p7 | 1:16348100 | ACTTGTCTGTAAGTC[A/C]TATCCTTGTACATGT | 54455 |
rs187953999 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16330403 | GTGGCAGCTACTTGG[G/T]GGCTGGGGTGGAAGG | 54455 |
rs188009830 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16287630 | TGGGCTCTTGCTATG[G/T]TGCTCAGGCTGGTCT | 54455 |
rs188013744 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16352758 | CTAACATTTAGCCAG[C/G]AATTAACTCACTTCT | 54455 |
rs188030169 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16317164 | GGCTCACACCCGTAA[C/T]CCCAGCACTTTGGGA | 54455 |
rs188077910 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16325896 | CTCCTAGAGTGCTGG[A/G]ATTACAGGCGTGAGC | 54455 |
rs188167486 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FBXO42 | GRCh38.p7 | 1:16266758 | TGTCATCATGGTATT[A/G]TGTGAAGTGACTGAC | 54455 |
rs188247954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16339930 | TGCGCTCCAGCCTGG[A/G]TGATAAAGCAAGACC | 54455 |
rs188279333 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | FBXO42 | GRCh38.p7 | 1:16323520 | TAAGGGACAGGGCCG[A/G]GCGCAGTGGCTCACG | 54455 |
rs188284895 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16304354 | AAACTCCTGACCTCA[A/G]GTGATCAGCCAACTT | 54455 |
rs188344896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16309222 | ACAGGCACGCGCCAC[C/T]ATACCCAGCTAATTT | 54455 |
rs188353462 | snp | A/G/T | 0.00637056 | 0.0560935 | intron-variant | FBXO42 | GRCh38.p7 | 1:16341928 | ATGAGCCAAGATCGC[A/G/T]TCATTGTACTCAAGC | 54455 |
rs188388955 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16299993 | CTTTACTTATTGCCT[A/G]TTTTTTATTTAAGAC | 54455 |
rs188409487 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16260275 | GTGTAATGGCACGAT[A/C]TCGGCTCACTGCAAC | 54455 |
rs188415804 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16281088 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 54455 |
rs188510078 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16302894 | AACCGCCCCCATGAT[C/T]CAGTCTCCTCCCACC | 54455 |
rs188515979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16338720 | AACCTAGCTTCCCCA[C/T]TGATAAACAAAAATA | 54455 |
rs188521715 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16258308 | CAGTCCTGAAGAGTA[C/T]AGGGTGAGCATCTAA | 54455 |
rs188550311 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16262605 | CCAGGTTCAAGAATC[A/G]CTTGAACCTGGGAGG | 54455 |
rs188683061 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | FBXO42 | GRCh38.p7 | 1:16335786 | GCAGGAGAATCGCTT[A/G]AACCTGAGAGGCAGA | 54455 |
rs188704536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16300460 | CATCTTTTCCATGGT[A/G]TATGGAGCATTCAAT | 54455 |
rs188716954 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16281370 | ACCAGCACCTCATCC[C/T]TAACAACCTCTCAAG | 54455 |
rs188717276 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FBXO42 | GRCh38.p7 | 1:16320006 | TCAACATGACTGACT[C/T]GCTAGAGGGAGGCCT | 54455 |
rs188752680 | snp | A/G | 0.00199481 | 0.0315187 | downstream-variant-500B | FBXO42 | GRCh38.p7 | 1:16246687 | TTTTGTATTTTTAGT[A/G]GAGACAGGGTTTCAC | 54455 |
rs188785063 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16322306 | TACTAGGCCAGGCGT[C/G]ATGGCTCACACCTGT | 54455 |
rs188815744 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16283113 | AGGTGATCTGTTATC[C/T]AATTTTTATGAACAG | 54455 |
rs188871062 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FBXO42 | GRCh38.p7 | 1:16291750 | AATCATCACTCACTG[C/T]AGCCTTGAACTCCTG | 54455 |
rs188895032 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FBXO42 | GRCh38.p7 | 1:16328872 | CAAAACAAAAGAAAA[C/T]TGATGGGATTGGCCG | 54455 |
rs188896775 | snp | A/C | 0.0134861 | 0.0810011 | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16353624 | GTTCTTGGTTCGCTG[A/C]AACCTCTGTCTTTCA | 54455 |
rs188911298 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16345136 | AACATATATATATAT[G/T]TTCTGAGCCAGGCGC | 54455 |
rs188916871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16289283 | GGGGTGCAAACCTGT[A/G]GCTCCAGCTATGCAG | 54455 |
rs188933637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16271168 | GAATGCAGCAGGCAA[C/T]GAGGTCAGAGAGATG | 54455 |
rs189036090 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FBXO42 | GRCh38.p7 | 1:16331051 | GCTTGAACCAGGAGG[C/T]GGAGGTTGCAGTGAG | 54455 |
rs189045897 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16313772 | GCCTTGTTCCCCCAG[C/G]AAAGAACACATTGAG | 54455 |
rs189072803 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FBXO42 | GRCh38.p7 | 1:16253011 | ATGGAAATAGTCTTG[C/T]ATACTCCTAGAAAAG | 54455 |
rs189076994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16293643 | CACTCAGTAGGCTCC[C/T]CCTATATTTGCCTAA | 54455 |
rs189081544 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16276024 | GTGATATTTATAAGT[C/G]AATAAACGACCCATC | 54455 |
rs189088776 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FBXO42 | GRCh38.p7 | 1:16338880 | CAGTGGCACAATCGC[A/G]GCTCACTGCAACCTC | 54455 |
rs189110829 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16350870 | CGCAACATGCCTATG[C/G]ATCAATGTAGATTGA | 54455 |
rs189124774 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16315506 | TTCAGGCATGTACAT[A/C]CAAGCTCTTTGTAAT | 54455 |
rs189144741 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | FBXO42 | GRCh38.p7 | 1:16273999 | GTTCAAAGAAAGAAG[A/C]CAGACATAAAATACT | 54455 |
rs189150661 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16312767 | TACATGTGTCAGGGT[A/T]GGGGATATATGAGAA | 54455 |
rs189164635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16284539 | ATAAAATCTGTCATC[C/T]TAAAAAAACGAGCTG | 54455 |
rs189264890 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16263730 | CTCCGTCTCAAGGAA[A/G]AAAACAAAAAAAAAC | 54455 |
rs189290200 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16334566 | AAAATAACCCACAAC[A/T]AACAACATAATTTCA | 54455 |
rs189365798 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16350339 | ATTAGCAAATTGATA[A/T]GCAAAGTAGCTCTCC | 54455 |
rs189424606 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16331458 | TAATAATAATTTAAT[C/T]AAAAAGTAAAAACCG | 54455 |
rs189450929 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | FBXO42 | GRCh38.p7 | 1:16340400 | CTCGGCTCACTGCAG[C/T]CTCCGCCTCTCCCAG | 54455 |
rs189518545 | snp | A/T | 0.0225045 | 0.103662 | intron-variant | FBXO42 | GRCh38.p7 | 1:16303929 | TTTTTATATATATAT[A/T]TTTTTAAGAGACGGG | 54455 |
rs189533993 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | FBXO42 | GRCh38.p7 | 1:16323166 | GCTCACGCCTGTAAT[A/C]CCAGCACTTTGGGAG | 54455 |
rs189543850 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | FBXO42 | GRCh38.p7 | 1:16262957 | TTCAAGCAATCTGCC[C/T]GCCTCGGCCTCCCAA | 54455 |
rs189551779 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16283861 | GTTAATCTCTAAGCA[A/G]TTTTGAAAATCAGAA | 54455 |
rs189580679 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FBXO42 | GRCh38.p7 | 1:16319241 | AAAAAGTGACAGACC[A/G]GGGAGAGCAGAGAAC | 54455 |
rs189605069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16328298 | AACCTAAGTAACTTT[A/G]GAAATAAGGGGCATC | 54455 |
rs189635539 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16260505 | TGAGCCACCGCGCCT[C/G]GCCCAATTACTATGC | 54455 |
rs189643933 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16325729 | TGAACTCACTCGAGC[A/G]ATTCTCCTACCTCAG | 54455 |
rs189655742 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16341839 | AGCCAGGCATAGTGG[C/T]GTCTGCCTGTAATCC | 54455 |
rs189656764 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FBXO42 | GRCh38.p7 | 1:16288679 | TTAAGAAGTCTTGGC[C/T]GGGCGCAGTGGCTCA | 54455 |
rs189731823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16323896 | AGGAACCCACAGTCA[C/T]CCCACAGCATGAGGG | 54455 |
rs189796223 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FBXO42 | GRCh38.p7 | 1:16279110 | AGTTCTAGCACTGGT[C/T]GTGCTCCCTATCCAA | 54455 |
rs189807280 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16295613 | GGCCAGGCTAATCTC[A/G]AACTCCTGACCTCAG | 54455 |
rs189828679 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FBXO42 | GRCh38.p7 | 1:16277186 | ATATTTGAAAGGCAC[A/G]TGTGTCCTCTTGTTA | 54455 |
rs189846230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16255587 | TGATCCACCCACCTT[A/G]GCCTCCCAAAATGCT | 54455 |
rs189890660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16344676 | ATACATACATAGGAT[A/G]AAGCAAATAAATGTT | 54455 |
rs189907235 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16270156 | CCACCACGCCCAGCC[A/T]CTTTCTCTTCTTATA | 54455 |
rs189912508 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FBXO42 | GRCh38.p7 | 1:16310962 | CTGGGCAACAGAGCC[A/G]GACTCCATCTCAAAA | 54455 |
rs189963889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16318358 | AGGAGGCAGACGTTG[C/T]AGTGAGCTGAGGTCG | 54455 |
rs190063524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16259653 | CGCCTGTAATTCCAG[C/T]TACTCAGGAGGCTGA | 54455 |
rs190101696 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16351289 | ACAGAAACACAATCG[A/C]AGTCTCCCAATTAGC | 54455 |
rs190102354 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16263987 | GGCTAATTTTTGTAT[G/T]ATTAGTAGAGACGAG | 54455 |
rs190105987 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16331834 | GGCGCGCAGATCACC[C/T]GAGGTCAGGAGTTCG | 54455 |
rs190106432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16305022 | CTACAATATATTTAG[A/G]CTGACACTTTTCCCT | 54455 |
rs190124580 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | FBXO42 | GRCh38.p7 | 1:16297468 | TTTTAAAATTACCAA[A/G]GAAATTAGACAAAAC | 54455 |
rs190141000 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | FBXO42 | GRCh38.p7 | 1:16316031 | GAAAATTAGCTGGGC[A/G]TGGTGGCACATGCCT | 54455 |
rs190226681 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16299779 | CCTCCCGAGTAGTTT[C/G]GACCACAGGCACGCG | 54455 |
rs190236970 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16333904 | AGAAAACTAATTTCC[A/T]TCTCTGACCTTCTAT | 54455 |
rs190275977 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16272541 | TGGGATTACAGGCGT[G/T]AGCCACCGTGCCCGG | 54455 |
rs190288455 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16248468 | TGGAAGGAATCAACA[C/T]GTTAACAGCTGGCTT | 54455 |
rs190358537 | snp | A/G/T | 0.00358891 | 0.0422285 | intron-variant | FBXO42 | GRCh38.p7 | 1:16284694 | AAAATTAGGCCAGGC[A/G/T]CAGGGACTCATGCCT | 54455 |
rs190431903 | snp | C/T | 0.031825 | 0.122064 | intron-variant | FBXO42 | GRCh38.p7 | 1:16331269 | ATACAAAAAATTAGC[C/T]GGGCATGGTGGCGGG | 54455 |
rs190450081 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16294130 | CAGTGGACACTATTT[C/G]TCCATCACACCAACC | 54455 |
rs190454215 | snp | C/T | 0.000324086 | 0.0127255 | intron-variant | FBXO42 | GRCh38.p7 | 1:16253593 | GTCCTAACTGAAAGA[C/T]GCTACAGTGTTTGCT | 54455 |
rs190511185 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16354259 | GTGATCCACTCACCT[C/T]GGCCTTCCAAAGTTC | 54455 |
rs190538927 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16347597 | CTGTGGCTCACGCCT[A/G]TAATCCCAGCACTTT | 54455 |
rs190575602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16329949 | GCAAGATACCATCTC[A/G]GGGCGGGGGAAACAA | 54455 |
rs190579269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16291642 | TCACCTCAGCCTCTC[A/G]AAGTGCCAGGATTGT | 54455 |
rs190583374 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | FBXO42 | GRCh38.p7 | 1:16312611 | CATTATACATTCATC[A/C]AAACCCATAGAATGC | 54455 |
rs190589112 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16249231 | CCTATGCCCAGGCCA[C/T]GGTTGAGACTAGTAA | 54455 |
rs190598387 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16273532 | ATGTTGATGGCAGCT[A/G]TATTCAAAGTAGAAA | 54455 |
rs190667005 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16315070 | CTAGATTTTATAACC[A/T]TAATACATTTAAGGG | 54455 |
rs190688756 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16276645 | TAAAGTTAATCTATA[C/T]AGCATTGGAGATATA | 54455 |
rs190739363 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16286149 | GCTGATTTTACAGGC[A/G]TGAGCCACCATGCCT | 54455 |
rs190746399 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16277582 | ATACAAAAACTAGCC[A/G]GGCGTGGTGGTATGC | 54455 |
rs190751052 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16321697 | AGCTCGCAAGGGTTT[G/T]TTTTTTTTTTTTAAA | 54455 |
rs190783488 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FBXO42 | GRCh38.p7 | 1:16261847 | TAGCTGGGACTACAG[A/G]CACCCCCCGCCATGC | 54455 |
rs190787508 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16345648 | AGGTCAGGAGATCGA[C/G]ACCATCCTGGCTAAC | 54455 |
rs190787608 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16301524 | AAAAATTAGCTGCGC[A/G]TGGTGGCAGGCACCT | 54455 |
rs190793597 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16329317 | GGCCAGGTGCTGTGG[C/T]TCATGCCTGTAATCC | 54455 |
rs190793901 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16282148 | CATATTATACAGTAA[A/G]ACTGCAAGAAGATAT | 54455 |
rs190897242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16324943 | CCTTTGCCACTTACA[A/G]AATTACCTTTAGAGC | 54455 |
rs190901179 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16272476 | GTTAGTCAGGCTGGT[C/T]TCGAACTCCTGACCT | 54455 |
rs190910648 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16341668 | GGTGGTCCCTACTAT[C/T]TGATATTCTTAAAAG | 54455 |
rs190916981 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | FBXO42 | GRCh38.p7 | 1:16285359 | GCTCACTGCAACCTC[C/T]GCCTCCTGGGTTCAA | 54455 |
rs190928884 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16305705 | GGTGATAGAGTGAGA[A/C]CTTGTCTCAAAAACA | 54455 |
rs190929916 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16264919 | GCAAAGAAGCTGGTT[A/G]AACAGTGAAGCAGTT | 54455 |
rs190967578 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | FBXO42 | GRCh38.p7 | 1:16307225 | GATGAGAGGCCAGGC[A/G]CAGTGGCTCACACCT | 54455 |
rs191004047 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16265699 | GTTCTGAGTAATCAA[C/G]AAATCCAACCTAAAG | 54455 |
rs191036578 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16309528 | TAAAACTCCTCGAAG[A/G]TAACAGGAGAAAATC | 54455 |
rs191046716 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16342120 | TAACTCTACAGGCCA[A/G]GTGCAGTGGCTCACG | 54455 |
rs191137496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16290144 | GTCATCCCAACACTC[A/G]TCACCACTCTACCTC | 54455 |
rs191144413 | snp | A/C | 0.00398564 | 0.0444627 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16247362 | GGATCACCACAAGGA[A/C]AAGGACAGACAGACA | 54455 |
rs191193489 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16317376 | TGAGCAGAGATCACT[A/C]CGCACTCCAGCCTGG | 54455 |
rs191194356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16291189 | CCAATCTACCTACCT[C/T]GATGCACTAAAATGA | 54455 |
rs191207034 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16329528 | GGCAGAGGTTGCAGT[G/T]AGCCAAGATCGCACC | 54455 |
rs191222846 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16258977 | ACTCCTGGCCTCAAG[C/T]GATCCTCCCGCCTCA | 54455 |
rs191227036 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16298941 | ACAGATAACTTCTTG[A/G]CAGCTGCTTCCTTAG | 54455 |
rs191227334 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16278305 | AGGTTGCAGTGAGCC[A/G]GAGATCACGCCATTG | 54455 |
rs191294548 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16326038 | TGTGTGTGTGTGTGT[C/G]TGTGTGTGTGTCTGT | 54455 |
rs191310563 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16287205 | ATATCAAGCACACTC[C/G]CAACTCTGGGTCTTT | 54455 |
rs191423334 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16312369 | TCTGTCTCAAAAAAT[A/G]AGGAGGAAACTTAAA | 54455 |
rs191505736 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FBXO42 | GRCh38.p7 | 1:16343932 | GCATTGAGCCATAAT[C/T]ACACCACACTTTAGC | 54455 |
rs191507294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16318003 | GGCAAAATTTATGCT[A/G]TTACAAGTGAGGTAT | 54455 |
rs191519385 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16353512 | TTGGTGTCCACAATC[C/T]CTTATCATAACCCAG | 54455 |
rs191521123 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16333510 | GTAGTCCCAGCTATG[C/T]GGGAGGCTGAGGTGG | 54455 |
rs191542653 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FBXO42 | GRCh38.p7 | 1:16299707 | TGGAGTGCAGTGGCA[C/T]GATCTCGGCTCACTG | 54455 |
rs191545379 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16321230 | TTGCTAACTTGGCCC[C/T]AGCCACAGATGCCAA | 54455 |
rs191549553 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | FBXO42 | GRCh38.p7 | 1:16281750 | TAACCTCCACCTCCC[A/G]GGTTCAAGCGATTCT | 54455 |
rs191605166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16346970 | AGCTGGTCTTGAACT[C/T]CTGACCTCAAGTGAT | 54455 |
rs191672911 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16267740 | AGACAAAACTTGTCT[A/G]GATCTCAGGATTCAG | 54455 |
rs191692846 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16252945 | AAGCAGAAACAAAGG[C/T]CAGAAAATACAAAGG | 54455 |
rs191764029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16336228 | CAGGCATGAGCCACC[A/G]CGTCTGGCCTAATCT | 54455 |
rs191811767 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16301043 | AGCTGGATTACAGGC[A/G]TGCGCCCACCACGCC | 54455 |
rs191828123 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16261683 | GTTCAGCAACCAGAA[C/G]TCAAGGATACAGGTA | 54455 |
rs191855074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16337524 | CCAATCATAGGACTC[C/T]ATTTATTCTTTTTAA | 54455 |
rs191864104 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16322139 | ATGTTACTAGATGTT[A/G]TCAAAATATTTTATT | 54455 |
rs191865125 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16311624 | AGCGCATGAAAATAC[A/G]CTCCATATCATTTGT | 54455 |
rs191869441 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16302633 | TCCTGCCTCAGCCTC[A/C]CAAGTAGCTGGGACT | 54455 |
rs191874472 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16274891 | CACCATGCCCAGCTA[A/T]CAAATTATGTCTTAA | 54455 |
rs191876041 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16292876 | GGATGCTTAAGCTGA[C/G]AAGATCTTCTATATT | 54455 |
rs191877396 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | FBXO42 | GRCh38.p7 | 1:16337858 | CACTGTACTCCAGCC[A/T]GGGAGAAAGAGCGAG | 54455 |
rs191984534 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | FBXO42 | GRCh38.p7 | 1:16257998 | GAATACTTTTTTTTT[A/T]AAAATCTTTTTTTTT | 54455 |
rs191984641 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16297974 | CTCATGCCTGTAATC[C/T]CAGCACTTTGGGAGG | 54455 |
rs191989652 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FBXO42 | GRCh38.p7 | 1:16258508 | AATACAGGCAAGCAC[C/T]ACCATGCCCGACTAA | 54455 |
rs192117999 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16332782 | CCGACCTCAAGTCAT[A/C]TGCCTGCCTCGGCCT | 54455 |
rs192188229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16349587 | AATTCAGGGCCGGGC[A/G]CAGTGGCTCAAGCCT | 54455 |
rs192196861 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | FBXO42 | GRCh38.p7 | 1:16331053 | TTGAACCAGGAGGCG[A/G]AGGTTGCAGTGAGCC | 54455 |
rs192236565 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16352929 | TTACTAGCTCCACTT[C/T]TCAGATGAGGAAACT | 54455 |
rs192242285 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | FBXO42 | GRCh38.p7 | 1:16287807 | TCAAACTCTCGGCCA[A/G]GCACAGTGGCTCATG | 54455 |
rs192309381 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16278044 | GACACCCTGTATCAA[A/G]AAATAAATAATTTTT | 54455 |
rs192310792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16317018 | GGATGCAGTGGCTCA[C/T]GCCTGTAATCCCAAC | 54455 |
rs192353801 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16339407 | AACCTCCGCCACCTG[C/G]GTTCAAGTGATTCTC | 54455 |
rs192374184 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FBXO42 | GRCh38.p7 | 1:16304051 | CTCAGGTGATCCGCC[C/T]GCCTTGGCCTCCCAA | 54455 |
rs192376143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16348390 | CAACACCAATCCACA[C/T]AGATTCTATAAAAGT | 54455 |
rs192385002 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FBXO42 | GRCh38.p7 | 1:16284247 | TGGCCAGGATTTCCA[A/G]TGGTTTCTGTTCTAC | 54455 |
rs192391390 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16323404 | GCCCAGGTGACAGTG[C/T]GAGACTCCGTCTCAA | 54455 |
rs192397912 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16263387 | CGCCAAGCTTGCATT[C/G]AGCCAAGATCACGTC | 54455 |
rs192402801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16327725 | TTTTGTTTTTTAAGA[C/T]GGAGTCTCGCTCTGT | 54455 |
rs192459937 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16308129 | GAGCCAAGAAATAGA[A/C]CCATACAAATACAGT | 54455 |
rs192507203 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime | FBXO42 | GRCh38.p7 | 1:16352449 | GCCGCCGCCGCAGCT[A/G]CTGCTGCTCAGGCCG | 54455 |
rs192525607 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16268703 | GCACAGCAGCTCACG[A/C]CTGTAATCCCAGCAC | 54455 |
rs192571435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16278418 | TTTCAATGTTAGCAC[C/T]GACGTTTGGGACCTG | 54455 |
rs192637479 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16332933 | TGAGAAGAGTAGTGG[C/G]TTTTTCCAACAGATT | 54455 |
rs192652591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16310444 | GCTGAATTTGGAGGA[C/T]TGCTTGAGCCTGGGA | 54455 |
rs192658747 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | FBXO42 | GRCh38.p7 | 1:16343067 | ATATAATAAATTACT[G/T]AATCTCAGGTATTCT | 54455 |
rs192664855 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16269941 | TCTCACTGCAACCTC[C/T]GCCTCCCAGGCTCAA | 54455 |
rs192676070 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16309985 | CAGATCACAAGGTCA[A/G]GAGATCGAGACCATC | 54455 |
rs192692486 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16287308 | TCCTTGTTCTAATGT[C/T]GCCTTCTCTCTGATT | 54455 |
rs192695478 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16326399 | TTTAAAATTTCTTCT[G/T]GAGGCCAGGTGCAGT | 54455 |
rs192718439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16262375 | CCTTAATTCCCTCTC[A/G]ATGATCTTAAAGCAA | 54455 |
rs192782038 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16330750 | GTTTGAGACCAGCCC[A/G]GCCAACACTGTGAAA | 54455 |
rs192847392 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FBXO42 | GRCh38.p7 | 1:16259511 | GCTCACACCTGTAAT[C/T]CCAGCACTTTGGGAA | 54455 |
rs192864605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16322813 | CCCCACTTACTTCAG[A/G]AAGATTTTGTAAAGA | 54455 |
rs192870727 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16283357 | AACTGCAAAGAAAAA[G/T]AAAATCCTTGGGAAA | 54455 |
rs192914235 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16282294 | GCAGTGGCGCGATCT[C/T]GGCTCACTGCAACTT | 54455 |
rs192999022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16349342 | TCCCCAGCCATACTA[C/T]ATGCAACTTCAGACC | 54455 |
rs193005861 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16313493 | TGAGAAGTGAAACCA[A/T]GTATTTCCACATTGC | 54455 |
rs193034663 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16274040 | GACGTCCATTTACAC[C/G]AAGTTCAAGAACACA | 54455 |
rs193035804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16312830 | GACAGAATCTCTGTC[C/T]GTCATCCAGACTCGA | 54455 |
rs193063216 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16303014 | TGCTTGAGCTCAGGG[A/G]TTCGAGACCAGTCTG | 54455 |
rs193069094 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16338769 | ACATTTTAACAAGAT[C/G]CTGTGATGGAATGGA | 54455 |
rs193083547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16262645 | CAGTGAGCCCAGACC[A/G]TGCACCAGTACACAT | 54455 |
rs193140595 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | FBXO42 | GRCh38.p7 | 1:16299938 | GTGAGCCACCATGCC[C/G]GGCCACACTCAACTA | 54455 |
rs193141740 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16333971 | ACTGTATCAACTGTA[C/T]GGTAAAAATAATAAT | 54455 |
rs193161278 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16259666 | AGCTACTCAGGAGGC[C/T]GAGGCACAAGAATTG | 54455 |
rs193213373 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | FBXO42 | GRCh38.p7 | 1:16330440 | TGAGCCCAAGAGGTG[C/G]AGGCTGCAGGGAGCT | 54455 |
rs193222188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16292109 | CATTTTGTTAGAAAA[C/T]TACTTTAAACATTCA | 54455 |
rs193223563 | snp | C/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251620 | GGCCGTTAACACAAG[C/G]AGCTTCATCCATGCT | 54455 |
rs193287195 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16354074 | CTCACTGCAACTTCC[A/G]CCTCCTGGGTTCAAC | 54455 |
rs193291261 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | FBXO42 | GRCh38.p7 | 1:16318600 | CATTATACACAAAGT[C/G]TGAGGTAAAACCAGT | 54455 |
rs193298440 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FBXO42 | GRCh38.p7 | 1:16280678 | CTTCTTGGGGGCTGA[A/G]GAAAGAGGATCACCT | 54455 |
rs199507808 | snp | A/G | 4.94214e-05 | 0.00497074 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250724 | TGGATAGTACTTCAC[A/G]TTCTGTTTCTTGTCC | 54455 |
rs199549845 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16288446 | AAAAAATAAAAATAA[A/T]AATAAAAATAATAAT | 54455 |
rs199564411 | in-del | -/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16288958 | TGAGACTATGTCTCA[-/T]AAAAAAAAAAAAAAA | 54455 |
rs199564466 | snp | A/G | 6.59914e-05 | 0.00574381 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251015 | TTGGGCAGGCCCTGG[A/G]CGAGGGATGGGCACT | 54455 |
rs199568380 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16293219 | TCCACCTCCTGGGTT[C/G]ATGAGATTCTCCTGC | 54455 |
rs199618049 | in-del | -/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16342599 | AAAAAAAAAAAAAAA[-/G]TTATAGTAATACCAT | 54455 |
rs199646590 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16323310 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCCA | 54455 |
rs199647911 | snp | A/C/T | 1.69338e-05 | 0.00290974 | intron-variant | FBXO42 | GRCh38.p7 | 1:16315159 | TAAACCTTTCTCCTA[A/C/T]CCACAGTACCTTTGA | 54455 |
rs199656455 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16313328 | AGAAAAGAAAACAAA[C/G]AAAGAAAGAAAGAAA | 54455 |
rs199672270 | in-del | -/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16279859 | TTTTTTTTTCTTTTT[-/C]TTTTTGAGACAGAGT | 54455 |
rs199758833 | in-del | -/T | 0.0103295 | 0.0711199 | intron-variant | FBXO42 | GRCh38.p7 | 1:16266180 | GTTTTCAAAGTATAG[-/T]TTTTTTTTAAAAAAA | 54455 |
rs199788433 | snp | C/T | 0.00199792 | 0.0315431 | utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16315426 | CTGGCCATGACATTC[C/T]ACTCAACAGCTGTAA | 54455 |
rs199826620 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16350743 | CAGAGTGAGAAACTG[A/C]AAAAAAAAAAAAAAA | 54455 |
rs199863983 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16308569 | CAGTGGCACGATCCC[C/T]GTTCACCACAATCTC | 54455 |
rs199884583 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16281479 | CTTTTTTTGTTTTTT[G/T]TTTTTTTTGAGATGG | 54455 |
rs199897129 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16346666 | GCACTCCAGCCTGGG[A/C]GACAGAGCTAGACTC | 54455 |
rs199941117 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16326060 | TGTGTCTGTGTGTGT[C/G]TGTGTGTGTTTTGAG | 54455 |
rs199959930 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16279854 | AATGGTTTTTTTTTT[C/T]TTTTTTTTTTGAGAC | 54455 |
rs200024078 | snp | A/C | 0.000367858 | 0.0135571 | intron-variant | FBXO42 | GRCh38.p7 | 1:16255865 | GAAGTCAGCACCACA[A/C]ACTTTATGTAAAAAT | 54455 |
rs200039642 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16270707 | AAAAAGAAAAGAAAA[A/G]AAAGAAGAAAAGATA | 54455 |
rs200092981 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16253641 | CCTGAGCACCTGAGA[C/T]TGGCCACCTCGAGGA | 54455 |
rs200141706 | in-del | -/AC | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16348328 | CTACAGCACTAAGGT[-/AC]AAATAACTTGTACTG | 54455 |
rs200155262 | in-del | -/TTTTCTTTTTTTTTT | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16282216 | GAATCAACTGAGACA[-/TTTTCTTTTTTTTTT]TTTTCTTTTTTTTGA | 54455 |
rs200166365 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16343953 | ACACTTTAGCATGGC[-/A]AAAAAAAAAAAAACA | 54455 |
rs200182529 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16252786 | TCAACCTGCTTTTTT[A/G]TTCCACTGCCCTCTC | 54455 |
rs200191307 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16329160 | AGAGTGAGACTCTGT[C/G]TCAAAAAAAAAAAAA | 54455 |
rs200255191 | in-del | -/AAAGAAAGAAAGAAAG | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16313325 | AAGAGAAAAGAAAAC[-/AAAGAAAGAAAGAAAG]AAAGAAAGAAAGAAA | 54455 |
rs200267691 | in-del | -/AAT | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16331452 | AATAATAATAATAAT[-/AAT]TTAATTAAAAAGTAA | 54455 |
rs200270786 | snp | C/T | 3.30431e-05 | 0.00406454 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16253692 | GTTCGGCTTGGACCA[C/T]GCCCACTGCTCAAGG | 54455 |
rs200284191 | snp | C/T | 0.00128408 | 0.0253059 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250841 | ATTAAATACTTTCCA[C/T]TTGACCCGCCCCTTC | 54455 |
rs200308098 | in-del | -/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16341973 | GAAATTCCGTCTCCA[-/G]AAAAAAAAAAAAAAA | 54455 |
rs200336883 | snp | A/G | 0.000230757 | 0.0107389 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16305900 | CTTCATGAAACCATG[A/G]TAACACTGATGGGCT | 54455 |
rs200338156 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16293217 | CCTCCACCTCCTGGG[A/T]TCATGAGATTCTCCT | 54455 |
rs200366558 | in-del | -/GTCCAATG | 0.0178098 | 0.0926698 | intron-variant | FBXO42 | GRCh38.p7 | 1:16295762 | GTAACCACACATAAA[-/GTCCAATG]GTCCAATGTGATTGA | 54455 |
rs200383567 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16319578 | CATTCCCCAAAAGCA[A/G]AGAAGAGTATTATAA | 54455 |
rs200397205 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16283507 | AAGTTTTTTTTTTTT[G/T]TTTTTTTTTTGAGAC | 54455 |
rs200464601 | in-del | -/A | 0.0345262 | 0.126772 | intron-variant | FBXO42 | GRCh38.p7 | 1:16322071 | CTACCTGGGACATGT[-/A]AAAAAAAATTACATC | 54455 |
rs200466082 | in-del | -/GA | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16270747 | TCCCTTACTTACCAT[-/GA]GATACACACACACAC | 54455 |
rs200470502 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16311376 | ACTTGTAGTCCCAGC[C/T]ACTTGGGAGGCTGAG | 54455 |
rs200516839 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16333446 | GTGAGACCCCCCCCC[C/T]CCATTTCCAAGAAGA | 54455 |
rs200524530 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16263734 | GTCTCAAGGAAAAAA[A/C]CAAAAAAAAACCGAA | 54455 |
rs200580135 | in-del | -/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16281473 | TTTTTCTTTTTTTGT[-/G]TTTTTTTTTTTTTTG | 54455 |
rs200591476 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16252333 | GGCCCCATGCTCTTC[A/G]TTTTCTACCTTGAGT | 54455 |
rs200599044 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16293220 | CCACCTCCTGGGTTC[A/C]TGAGATTCTCCTGCC | 54455 |
rs200632091 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16270708 | AAAAGAAAAGAAAAG[A/G]AAGAAGAAAAGATAA | 54455 |
rs200632149 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16349672 | TCAAGACCAGCCTGG[C/G]CAACATAGTGAAACC | 54455 |
rs200644777 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16345734 | GCGCCTGTAGTCCCA[A/G]CTACTCGGGAGGCTG | 54455 |
rs200686024 | snp | C/T | | | missense, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16315372 | ACAGTTTCTTCCTGG[C/T]CCACAGCCATGAAAC | 54455 |
rs200691798 | in-del | -/T | 0.0581099 | 0.160244 | intron-variant | FBXO42 | GRCh38.p7 | 1:16306708 | TGTTTTGTTTATTTA[-/T]TTTTTTCTTTAGACA | 54455 |
rs200697954 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16350753 | AACTGCAAAAAAAAA[A/G]AAAAAAAGAAAGAAA | 54455 |
rs200714545 | snp | A/G | 0.00199792 | 0.0315431 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250967 | GTGGTGGCCCAGGCG[A/G]CGAGCAATGGGAGGT | 54455 |
rs200746459 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16338377 | AAAAAAAAAAAAAAA[A/G]AATAACAATGTTGCA | 54455 |
rs200896198 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16279720 | AGGAAAAGAAAGCAA[C/T]AGACTATAAAAAAGA | 54455 |
rs200914545 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16329183 | AAAAAAAAAAAAAAA[C/T]AAAATTGATGGGATT | 54455 |
rs200915131 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16324834 | AAATCAAAAAACAAC[A/C]ACAAAAATAAAGAAG | 54455 |
rs200961361 | snp | A/C/G/T | 0.00032942 | 0.0128301 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16305807 | TAAATACTTACTGTG[A/C/G/T]GAGAAGCGCTGAGTG | 54455 |
rs200974614 | in-del | -/TT | | | downstream-variant-500B | FBXO42 | GRCh38.p7 | 1:16246523 | CTTTTTTTTTTTTTT[-/TT]GAGACAGTCTAACTC | 54455 |
rs200980604 | in-del | -/ACACACACACACACACACACACACAC | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16270752 | TACTTACCATGAGAT[-/ACACACACACACACACACACACACAC]ACACACACACACACA | 54455 |
rs201046928 | snp | A/G | 8.24409e-05 | 0.00641979 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250697 | TCGTACAAAGTACAA[A/G]GCGTTTGTTTTTGGA | 54455 |
rs201081204 | in-del | -/AA | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16282538 | GCCATTTTCTCTTTT[-/AA]AAAAAAAAAAAATGC | 54455 |
rs201084614 | in-del | -/G | 0.0182019 | 0.0936463 | intron-variant | FBXO42 | GRCh38.p7 | 1:16287774 | ATTTAAGGGAAGTCA[-/G]GCCCTTTGTTTTCAG | 54455 |
rs201095369 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16350907 | TATTTATACTGGCTT[G/T]TCAAAAGCAAACAGT | 54455 |
rs201096764 | snp | C/T | 1.65029e-05 | 0.00287248 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251401 | GTCCTATTTTCAGGT[C/T]GTATCCTTCAGGAGC | 54455 |
rs201112591 | in-del | -/A | 0.0603597 | 0.1629 | intron-variant | FBXO42 | GRCh38.p7 | 1:16257486 | ACTGACCAAATTCTG[-/A]AAAAAAAACACTTTG | 54455 |
rs201129799 | snp | C/T | 6.58892e-05 | 0.00573936 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250848 | ACTTTCCATTTGACC[C/T]GCCCCTTCTCCTTGG | 54455 |
rs201151727 | in-del | -/ACACACAC | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16270752 | TACTTACCATGAGAT[-/ACACACAC]ACACACACACACACA | 54455 |
rs201209760 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16282235 | CTTTTTTTTTTTTTT[C/T]TTTTTTTTGAGACAG | 54455 |
rs201245585 | snp | C/T | 3.35926e-05 | 0.00409819 | missense, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16255798 | ATGGGAGGTGGCCCA[C/T]GGGTTGTCACAATGC | 54455 |
rs201268739 | in-del | -/AAT | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16331423 | CTGTCTCAAAAAGAA[-/AAT]AATAATAATAATAAT | 54455 |
rs201330433 | in-del | -/TA | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16303917 | GCCCGGGTAATTTTT[-/TA]TATATATATATTTTT | 54455 |
rs201457928 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16311087 | TCCCAACACTTTGGG[-/A]GAATGGCATGAACCC | 54455 |
rs201488530 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16265796 | AAAAAAAAAAAAAAA[C/T]ACATTTCAAGGCCTC | 54455 |
rs201506524 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | FBXO42 | GRCh38.p7 | 1:16301690 | AAAAAAAAACAACAA[A/C]AAAAAAAGAAACGGT | 54455 |
rs201523342 | snp | C/T | 0.00374888 | 0.0431322 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250852 | TCCATTTGACCCGCC[C/T]CTTCTCCTTGGTGTC | 54455 |
rs201529452 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | FBXO42 | GRCh38.p7 | 1:16299232 | TGGCCAGGCTGGTCT[C/T]GATCTCCTGACCTCG | 54455 |
rs201538698 | in-del | -/TTGTCTTG | 0.0138799 | 0.0821421 | intron-variant | FBXO42 | GRCh38.p7 | 1:16338399 | ATGTTGCATGACATC[-/TTGTCTTG]TTGTCTTGGATACAG | 54455 |
rs201555032 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16293218 | CTCCACCTCCTGGGT[G/T]CATGAGATTCTCCTG | 54455 |
rs201581586 | in-del | -/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16282534 | CCCGGCCATTTTCTC[-/T]TTTAAAAAAAAAAAA | 54455 |
rs201652491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16294741 | TTCCATGCCAAGGGA[A/G]TCACCTGGTAAGGAG | 54455 |
rs201658897 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16321460 | GTAAGCATACTAACT[C/T]AATGAATGTAATTTT | 54455 |
rs201669789 | snp | A/G | | | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251656 | CTGGAGACTGAGAGC[A/G]GTACTCTCGGGTTTC | 54455 |
rs201691034 | in-del | -/AT | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16318552 | AAAGAAAGCATACAC[-/AT]AGAGGCAGGCATCTC | 54455 |
rs201709602 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16288974 | AAAAAAAAAAAAAAA[-/A]GTTTTGTCAGTTTCT | 54455 |
rs201722675 | in-del | -/TTTTTTC | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16279848 | GTTGACAATGGTTTT[-/TTTTTTC]TTTTTTTTTTGAGAC | 54455 |
rs201738656 | snp | C/T | 0.000263971 | 0.0114855 | intron-variant | FBXO42 | GRCh38.p7 | 1:16255693 | CAGGCTCATATGGAG[C/T]AAACCAAATGTACTT | 54455 |
rs201791039 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16330761 | GCCCGGCCAACACTG[C/T]GAAACCCCGTCTCTA | 54455 |
rs201801002 | in-del | -/GTCTCT | 0.0577344 | 0.159793 | intron-variant | FBXO42 | GRCh38.p7 | 1:16269129 | TTTTTTTGTGACAGA[-/GTCTCT]GTCTCTGTCACCCAG | 54455 |
rs201843961 | in-del | -/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16348326 | CAACTACAGCACTAA[-/G]GTAAATAACTTGTAC | 54455 |
rs201865800 | in-del | -/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16312812 | CTTTTTTTTTTTTTT[-/T]GAGACAGAATCTCTG | 54455 |
rs201866845 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16280375 | ACAAAAAGCCTAAAT[A/G]TAATGTATCAAGGAT | 54455 |
rs201916377 | snp | C/T | 1.65575e-05 | 0.00287724 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251108 | TAGTGCTGCAGAGGC[C/T]GAGGGGCCTTTGGAG | 54455 |
rs201927676 | in-del | -/T | 0.0596104 | 0.162024 | intron-variant | FBXO42 | GRCh38.p7 | 1:16308151 | AATACAGTCCATTCA[-/T]TTTTTTTTTAATAGA | 54455 |
rs201966154 | in-del | -/T | 0.02016 | 0.0983543 | intron-variant | FBXO42 | GRCh38.p7 | 1:16263134 | ACATAACTTTATTCA[-/T]TTTTTTTTTAAGTTC | 54455 |
rs202012049 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16348010 | AAAAAAAAAAAAAAA[A/G]AAAAAAAGAAAAGAA | 54455 |
rs202042854 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16263735 | TCTCAAGGAAAAAAA[A/C]AAAAAAAAACCGAAA | 54455 |
rs202106738 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16307536 | AGCAAAAAAAAAAAA[C/T]ACGAACATATAACAA | 54455 |
rs202119251 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16323819 | AAAAAAAAAAAAAAA[C/T]AATAAGGGACAAGAA | 54455 |
rs202125859 | snp | A/G | 0.00199799 | 0.0315437 | intron-variant | FBXO42 | GRCh38.p7 | 1:16252231 | ACCTGACAAAGTAAT[A/G]TGGTTTTCCACAATT | 54455 |
rs202166367 | snp | C/T | 6.59163e-05 | 0.00574054 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16256725 | GTCCTTGTACACGAC[C/T]AGAGTTGCTCCAGCT | 54455 |
rs202191833 | in-del | -/TG | 0.0103295 | 0.0711199 | intron-variant | FBXO42 | GRCh38.p7 | 1:16282121 | TTACTGTAATAACAC[-/TG]AGAGAGCTCACATAT | 54455 |
rs202194004 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16339681 | ATACTTGCACAGCTG[A/G]ACAGATTATGAATTT | 54455 |
rs202197639 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16311505 | AAAAAAAAAAAAAAA[A/T]ATATATATATATATA | 54455 |
rs202213874 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16282286 | GCTGGAGTGCAGTGG[C/T]GCGATCTCGGCTCAC | 54455 |
rs202228189 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16325406 | GTCTATGTTTTGACC[-/A]AAAAAAAAGCCTAGA | 54455 |
rs267598147 | snp | A/G | 1.65803e-05 | 0.00287922 | FBXO42 | 1 | allele_origin=G(germline)/A(somatic) | 1:16251759 | CCCACTAGGAGCCTG[A/G]CTGAAGACCACCACA | 54455 |
rs367563942 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16281628 | TATGGATCACCATGC[C/T]TGGCTAATTTTCTTT | 54455 |
rs367642093 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16247066 | CACATGGGGTGTGCA[C/G]TGACATGAACCCTGG | 54455 |
rs367649113 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16296786 | CAATATTTTTAAGGT[C/G]TCTTCTGAACTCTGG | 54455 |
rs367651266 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16313212 | CAGTGACTTCTGCCA[C/G]AAAGATCGATCTAAG | 54455 |
rs367652157 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16268979 | ACACCCAGTTAATTT[C/T]TGTATTTTAGCAGAG | 54455 |
rs367656958 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FBXO42 | GRCh38.p7 | 1:16334289 | ATACAAAAAATTAGC[C/T]AGGTGTGGTGGCGGG | 54455 |
rs367659817 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16304643 | CGCTAAGCATAACAC[C/T]TTGACCACTCTGGAG | 54455 |
rs367665030 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16287278 | CCACATGGCTCACTT[A/C]TTGTACCCATCAAGT | 54455 |
rs367708220 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250741 | TCTGTTTCTTGTCCA[C/T]GAGTCCTCCAAATAT | 54455 |
rs367731516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16293368 | TCAGGTGATCCGCCC[A/G]CCTTGGCCTCCCAAA | 54455 |
rs367774106 | in-del | -/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16275151 | AAACATTCTGAGATT[-/T]CAGCAGTGGGATTTC | 54455 |
rs367840443 | in-del | -/AC | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16315095 | TAAGGGAGGAAAAAA[-/AC]TAAATTTGGAGTCTA | 54455 |
rs367870204 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16274175 | GTCAGGCATGGTGGT[A/G]TGCATCTGCAATCCC | 54455 |
rs367882080 | in-del | -/CT | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16260902 | GAGATGGGGGTCTCT[-/CT]GTGTTGCCCAGACTG | 54455 |
rs367895759 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16303994 | ATTTTTAGCAGAGAC[A/G]GGGTTGTACCATGTT | 54455 |
rs367900247 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16323738 | GAGATTGCAGTGAGC[C/T]GAGATCGTACCACTG | 54455 |
rs367905782 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16344992 | TAATCCTAGCTACTC[A/C]GGAGGCTGAGGCAGG | 54455 |
rs367942141 | in-del | -/AAG | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16328719 | ATACCTAGCACCCAG[-/AAG]TTCTTTCTAATACCG | 54455 |
rs367980693 | in-del | -/TACAGCACAA | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16348326 | AACTACAGCACTAAG[-/TACAGCACAA]GTAAATAACTTGTAC | 54455 |
rs368092012 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16334910 | AGGGTAAACAGTGAT[C/T]CTTAGTATCAGGAAG | 54455 |
rs368102155 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16310903 | TGCTTGAACCCAGAA[A/G]GTGGAGGTTGCAGTG | 54455 |
rs368108122 | snp | C/T | | | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16354396 | TGCAACCTCTGCCTC[C/T]CAGGTCCAAACGATT | 54455 |
rs368133759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16314500 | TAAAATGCAGGATCT[C/T]CTAGTCAGAGTTTGC | 54455 |
rs368139127 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16346460 | TTGGGAGTCCGAGGC[C/G/T]GGCGGATCATGAGGT | 54455 |
rs368158198 | snp | A/G | 1.70093e-05 | 0.00291622 | intron-variant | FBXO42 | GRCh38.p7 | 1:16253068 | CTTAGTAGCATGCAC[A/G]TGGGAATGCCACAGA | 54455 |
rs368198301 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16334358 | GAATGGCGTGAACCC[A/C/G]GGAGGCGGAGCTTGC | 54455 |
rs368202951 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FBXO42 | GRCh38.p7 | 1:16273601 | AAAAAAAAATGAGGG[C/T]CGGGCATGGTGGCTT | 54455 |
rs368244362 | snp | C/T | 8.49149e-05 | 0.00651538 | intron-variant | FBXO42 | GRCh38.p7 | 1:16253075 | GCATGCACATGGGAA[C/T]GCCACAGAAGCAATA | 54455 |
rs368251000 | snp | A/C | 0.000798403 | 0.0199641 | downstream-variant-500B | FBXO42 | GRCh38.p7 | 1:16246644 | AAGTAGTTGGGATTA[A/C]AGGTGCCTGCCACCA | 54455 |
rs368258945 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16276098 | TGAAAACTGGAAAAC[C/T]TGGCAGGGTGCGGTG | 54455 |
rs368347587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16274453 | GAGGTGAAGAAAGTT[C/T]TCGTATCTTGATCTA | 54455 |
rs368352281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16270421 | ATTAGGCCTAACAAC[C/T]GGACGCTGAAGTACT | 54455 |
rs368434839 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16336006 | GCGCAATCTCGGCTC[A/G]TTGCAACCTCACTGA | 54455 |
rs368539525 | in-del | -/TCTGTC | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16269138 | GACAGAGTCTCTGTC[-/TCTGTC]ACCCAGACTGGAGTG | 54455 |
rs368540783 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16292067 | TAATTGCAGATTAGG[A/G]TGAGGGAGTAACTAG | 54455 |
rs368543695 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FBXO42 | GRCh38.p7 | 1:16263483 | TTAAAAGCACACGGC[C/T]GGCCAGGCGTGGTGG | 54455 |
rs368613669 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16288216 | GCAGACGGATCACGA[C/G]GTCAAGAGATCGAGA | 54455 |
rs368636862 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16298373 | TGGTCCTCTTAGACA[C/T]ATCTTGACCTAGTAA | 54455 |
rs368638977 | snp | C/T | 1.64773e-05 | 0.00287026 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16256683 | ATAAGGGCTTGGCCG[C/T]GTCCAGCCACCAAAC | 54455 |
rs368646156 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16267726 | CATTCACTGGTATTA[A/G]ACAAAACTTGTCTGG | 54455 |
rs368679962 | in-del | -/AAG | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16323862 | AAAAATAAAAAGAAG[-/AAG]GGACTGGACTGAATG | 54455 |
rs368781850 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16315769 | CAAAGGGAAGAGCAA[C/T]TAGCCTCCTTGGCCA | 54455 |
rs368789337 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16258640 | AGGATTACAGGTGTA[A/C]GCCACTGTGCCTGTC | 54455 |
rs368798836 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16289069 | TCTTGCCTTCCTTCA[C/T]TTCCTAAATAGAAGC | 54455 |
rs368848015 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16338066 | AGATCAAGACCATCC[C/T]GGCTAACACAGTGAA | 54455 |
rs368932988 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16347365 | TACTAAAAATACAAA[-/A]TTAGCCAGGCATGGT | 54455 |
rs368957203 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16286322 | TTAATTGACTCACAG[C/T]TCCGCATTGCTGGGA | 54455 |
rs368982150 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16347290 | GGAGGCTGAGGCAGG[C/T]GGATCACTTGAAGAC | 54455 |
rs368982884 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16290008 | TTCTTGTTTCTTTCC[C/T]GTTACAATATAAGCT | 54455 |
rs368991453 | snp | C/T | 1.64814e-05 | 0.00287061 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251695 | GAGCTGGAGGAGTGG[C/T]ACTGATAGGTGATGG | 54455 |
rs368997762 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16253686 | AGAGATGTTCGGCTT[A/G]GACCACGCCCACTGC | 54455 |
rs369006634 | snp | A/G | 1.65312e-05 | 0.00287495 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251062 | AACTCTGGCTCCCAG[A/G]AGAGCCTGGAGAAGA | 54455 |
rs369068557 | in-del | A/CC | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16333445 | AGTGAGACCCCCCCC[A/CC]CCATTTCCAAGAAGA | 54455 |
rs369079656 | in-del | -/AC | 0.322721 | 0.23919 | intron-variant | FBXO42 | GRCh38.p7 | 1:16270752 | TACTTACCATGAGAT[-/AC]ACACACACACACACA | 54455 |
rs369096637 | in-del | -/GG | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16266165 | GCTATTTTCATGGCT[-/GG]GTTTTCAAAGTATAG | 54455 |
rs369102310 | in-del | -/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16296669 | AAAAAAAAAAAAAAA[-/C]AAAAACAAAAAACAC | 54455 |
rs369119134 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16280451 | AGAAAATCTGAATAG[C/T]GTATGCATTTTAGTT | 54455 |
rs369198261 | snp | A/C/G | | | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16352548 | GCGGCGGGATGGCGA[A/C/G]GGGCGGCCAGGGGGC | 54455 |
rs369198815 | in-del | -/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16323819 | AAAAAAAAAAAAAAA[-/G]AATAAGGGACAAGAA | 54455 |
rs369203819 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16299299 | TACAGGCACGAGCCA[A/C]CGCACCCAGCCCACA | 54455 |
rs369236314 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16277711 | GCCGGGTGACAGAGC[A/G]AGATTCTGTCTCAAA | 54455 |
rs369241703 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16263866 | CCCAGGCTGGAGTGC[A/G]ATGGCACAATCTTGG | 54455 |
rs369289501 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16342014 | AGGCGCAGTGGCTCA[C/T]GTCTGTAATCCCAGC | 54455 |
rs369393217 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16352153 | GTGGGATACGGGGCC[G/T]GCGTCAGACCCCGGG | 54455 |
rs369399731 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FBXO42 | GRCh38.p7 | 1:16299801 | AGGCACGCGCTACCA[C/T]GCCCAGCTAATATTT | 54455 |
rs369501342 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16266652 | GAGCCTCAAACTGGC[A/G]TGTGTATGGGGGGTG | 54455 |
rs369503132 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16309637 | ATGGTAGCTCACGCC[C/T]GTAATCCCAACACTT | 54455 |
rs369507814 | in-del | -/CA | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16281612 | AGCTTGGACTACAGG[-/CA]TATGGATCACCATGC | 54455 |
rs369515453 | snp | G/T | 1.83451e-05 | 0.00302857 | intron-variant | FBXO42 | GRCh38.p7 | 1:16255681 | AGTATTTACCTTCAG[G/T]CTCATATGGAGCAAA | 54455 |
rs369528808 | in-del | -/GA | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16279698 | CAAATGGGTAAAAGA[-/GA]ATAACAGGAAAAGAA | 54455 |
rs369539629 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16299758 | CAAGCGATTTTCCTG[A/C]CTCAGCCTCCCGAGT | 54455 |
rs369614438 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16305320 | CTGAGCCGAGGAGGT[C/T]GAGGCTGCAGTGACC | 54455 |
rs369628651 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16346561 | GGCGTGGTGGTGGGC[A/G]CATGTAGTCCCAGCT | 54455 |
rs369639248 | snp | C/T | 3.29533e-05 | 0.00405901 | intron-variant | FBXO42 | GRCh38.p7 | 1:16305759 | AAGTTTCTGGAAATA[C/T]GACCACAGGCAGGGT | 54455 |
rs369761788 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16302501 | GAGAAAGAGCACAGG[G/T]GAAACTGCCACCTTT | 54455 |
rs369771738 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16341734 | CCAGCGCTTTGGTAG[C/G]CCAAGGCGGGCGGAT | 54455 |
rs369815338 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16302050 | CTTTTTAGCATGCAG[C/T]CTCTCTCACACAGAT | 54455 |
rs369827056 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16256201 | GAAACGGCGGTTGCT[C/G]TCATTAAGAGATATA | 54455 |
rs369832187 | in-del | -/TAGT | 0.00597247 | 0.0543191 | intron-variant | FBXO42 | GRCh38.p7 | 1:16332115 | TCTCATTAGCTTTAA[-/TAGT]TAGTCACTTCTGATA | 54455 |
rs369862383 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16288092 | TGGAGTGAGCCGAGA[C/T]CATGCCATTGCACTC | 54455 |
rs369876482 | in-del | -/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16291118 | TATTACCTTCCTGTA[-/C]ATACTCTGTTAGAAG | 54455 |
rs369890728 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16326701 | AAAAAAAAAAAAAAA[A/G]AAAAAAATTATTCTT | 54455 |
rs369910695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16299312 | CACCGCACCCAGCCC[A/G]CATTTTTCTTCTCTA | 54455 |
rs369915198 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16309216 | GGGATTACAGGCACG[C/T]GCCACCATACCCAGC | 54455 |
rs369922494 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16278903 | CCTGCCTCAGCCTCC[C/G]GAGCAGCTGGGACTA | 54455 |
rs369923019 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16301675 | GACCCCATCTCAAAA[A/G]AAAAAAAACAACAAA | 54455 |
rs369961084 | snp | C/T | | | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16352552 | CGGGATGGCGAGGGG[C/T]GGCCAGGGGGCGGCG | 54455 |
rs369965037 | snp | A/G | 0.000724709 | 0.0190218 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16294859 | AGCAGCATTGCAGCT[A/G]CTCTGGGTACAGCCT | 54455 |
rs369992903 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16301001 | CCTCCCAGGTTCAAG[C/T]GATTCTCCTGCCTCA | 54455 |
rs370006116 | in-del | -/CTT | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16349287 | GGATTCAGTGCACTT[-/CTT]AACACTACATAGCAC | 54455 |
rs370013023 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16283618 | TTCCCTGCCTCAGCC[C/T]CCCGAGTAGCTGGGA | 54455 |
rs370018146 | in-del | -/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16311190 | TCAAAAAAAAAAAAA[-/G]GGGGGTCAAAGGCCT | 54455 |
rs370052562 | in-del | -/AA | 0.0182019 | 0.0936463 | intron-variant | FBXO42 | GRCh38.p7 | 1:16329508 | GAACTGCTAGAACCA[-/AA]GAGGCAGAGGTTGCA | 54455 |
rs370115804 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16262088 | AATTGGATACTTTTA[A/T]ATTATTGCTACTTTA | 54455 |
rs370119620 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | FBXO42 | GRCh38.p7 | 1:16325634 | TAAAGTATTCCACAA[A/C]CTACCCATCAATATA | 54455 |
rs370133377 | in-del | -/CATAC | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16261615 | TGGAAAAAAACTTAC[-/CATAC]AAGAACAAATGAGGT | 54455 |
rs370162132 | snp | C/G | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251783 | CACCACACACTGTCC[C/G]ACCTGGAAGACAAAG | 54455 |
rs370270945 | in-del | -/AC | 0.0123615 | 0.0776397 | intron-variant | FBXO42 | GRCh38.p7 | 1:16252456 | GATATGCGTTCCAAA[-/AC]ACACACACACAGAGT | 54455 |
rs370276425 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FBXO42 | GRCh38.p7 | 1:16334290 | TACAAAAAATTAGCC[A/G]GGTGTGGTGGCGGGT | 54455 |
rs370289414 | snp | C/T | 0.000181562 | 0.00952617 | intron-variant | FBXO42 | GRCh38.p7 | 1:16305964 | CAGACACTTAACTTA[C/T]CCATCAAATTATTAA | 54455 |
rs370306288 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16303660 | GCAACCTCCGCCTCC[C/T]GGGTTCAAGTGATTC | 54455 |
rs370330402 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16257749 | GCAATGATGCAATCT[C/T]GGCTCACTGCAACCT | 54455 |
rs370377403 | snp | A/C | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250717 | TTGTTTTTGGATAGT[A/C]CTTCACATTCTGTTT | 54455 |
rs370415316 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16256662 | TCTCTCTGGCTGGTG[C/T]AGGGGATAAGGGCTT | 54455 |
rs370432420 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16262436 | ATCACATGGGGTGTG[G/T]TGGCTCAAGCCTGTA | 54455 |
rs370479050 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16266992 | ACTTCGTAAGGGCAA[A/C]AACAAAAGCATGTTT | 54455 |
rs370490830 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16303274 | AAGAATGCAAGGCTA[C/G]TTGCATGTTTCAGAC | 54455 |
rs370516883 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16272408 | GGGATTACAGGCATG[C/T]ACCACCACGCCCAGC | 54455 |
rs370518431 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16270752 | TACTTACCATGAGAT[-/A]CACACACACACACAC | 54455 |
rs370538809 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16265381 | CAGGCATGAGCTACC[A/G]TGCCCGGCCTAAAAA | 54455 |
rs370546255 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16268512 | CCAGGTTGTTACAGG[A/G]CTGCAAAGGGCTACA | 54455 |
rs370562762 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16312785 | GGATATATGAGAAAT[A/C]GGTTTTGTTTTGCTT | 54455 |
rs370577502 | snp | A/G | 0.000307953 | 0.0124049 | intron-variant | FBXO42 | GRCh38.p7 | 1:16255852 | AGGAGGAAGTCAAGA[A/G]GTCAGCACCACACAC | 54455 |
rs370580104 | snp | C/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16353069 | CTTTACTTCCTACTA[C/G]CTAGGTTATAGGATC | 54455 |
rs370589026 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | FBXO42 | GRCh38.p7 | 1:16310023 | ACACAGTGAAACCCC[A/G]TCTCTACTAAAAATA | 54455 |
rs370603166 | snp | C/T | 6.58979e-05 | 0.00573974 | intron-variant | FBXO42 | GRCh38.p7 | 1:16305780 | CAGGCAGGGTGGAAT[C/T]TGCTTTCACAGTAAA | 54455 |
rs370792808 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16295645 | TGATCCACCCGCCTC[A/G]GCCTCTCAAAGTGCT | 54455 |
rs370803907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16296587 | CCCGGGAGGCGGAGG[C/T]TGCAGTGAGCCAAGA | 54455 |
rs370821328 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FBXO42 | GRCh38.p7 | 1:16333118 | CTTCTTGAGGTTCTA[C/T]CCCCTCCAGCCAATT | 54455 |
rs370845560 | snp | A/G | 3.31565e-05 | 0.0040715 | intron-variant | FBXO42 | GRCh38.p7 | 1:16252407 | CATCCTTGAATAGCT[A/G]TAAGAGAAAAAACCA | 54455 |
rs370895828 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16300646 | TTTGATAAGGTCTCT[A/T]ATTACGTAACTATGA | 54455 |
rs370917666 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16343995 | AGAAAACTGCAAAGG[G/T]ATCTTTTTTTTATTT | 54455 |
rs370922326 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16253474 | CCACTATAAATAATA[C/T]GACCCATTAGAAGTT | 54455 |
rs370960678 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16352643 | GGGAGCTAGGCCTCC[A/G]CACCCGCCTTCGCCG | 54455 |
rs371079903 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16308015 | CAAAGTCAGAAGATT[A/G]ATACCACCTGACTTC | 54455 |
rs371143450 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16326722 | AATTATTCTTGAGTT[A/C]ATTCTGATAGGTGAT | 54455 |
rs371151973 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16281613 | AGCTTGGACTACAGG[C/T]ATGGATCACCATGCC | 54455 |
rs371187887 | in-del | -/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16336366 | TTTTGTTTGTTTTTG[-/T]TTTTTTTTTTGAGAT | 54455 |
rs371285573 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16334460 | CTGATTCTACAGATA[A/C]GACTAATGACCTGAG | 54455 |
rs371294745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16279914 | GGCAGTGGTGCAATC[C/T]TGGCTCACTGCAACC | 54455 |
rs371298019 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250166 | GGTCCTCTGTGGTTT[C/T]AAGAGAAGGGGAAAA | 54455 |
rs371316313 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16306974 | GTGGCTCACTGCAAC[C/T]TCTGCCTCCCAGGTT | 54455 |
rs371333583 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16269247 | CACATGATATCATAC[C/T]CGCCTAATTTTCTAT | 54455 |
rs371355785 | in-del | -/ACACACACAT | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16270784 | CACACACACACACAC[-/ACACACACAT]ATAAAATTCCATTCT | 54455 |
rs371407035 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16307818 | TAGTCCATGTTCATG[A/G]ATAGGATAAGAAGAC | 54455 |
rs371407854 | snp | C/T | 0.000437904 | 0.0147905 | intron-variant | FBXO42 | GRCh38.p7 | 1:16253040 | AGAAGACAGGGGAAA[C/T]AGGTTTTGAACACTT | 54455 |
rs371420167 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16259160 | ATAGCCTTACTGTTC[C/G]TGGTCAAAAACATTT | 54455 |
rs371423952 | snp | A/G | 0.000131843 | 0.00811815 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16315203 | CTGTTTGCAGACAAG[A/G]GCCGCAGTTTTGTGT | 54455 |
rs371427308 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16277656 | CTTGAATCCAGGAGG[C/T]GGAGGTTGCAATGAG | 54455 |
rs371427927 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16350486 | GCACGGTGGCTCAAG[C/G]CTGGGGTGGGGCAGG | 54455 |
rs371467495 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16267042 | GAGGTAGGGATAAAA[A/G]GATAATTGAGAAAAA | 54455 |
rs371471319 | snp | C/T | 3.31345e-05 | 0.00407016 | intron-variant | FBXO42 | GRCh38.p7 | 1:16294775 | AAGATCAGCATTTCA[C/T]CTCTTACCTGAAGCC | 54455 |
rs371494892 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16318835 | AGCAAAGACGGCCAC[G/T]CAGGGGAATCTAGTA | 54455 |
rs371520499 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16261315 | TGAGGCCAGTGATAA[C/T]GATAAATCAATATAA | 54455 |
rs371539278 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16304661 | GACCACTCTGGAGTA[A/G]AGAAAAATCCAATGA | 54455 |
rs371545532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16339399 | CTCACTGCAACCTCC[A/G]CCACCTGGGTTCAAG | 54455 |
rs371548731 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16339793 | CTTTGCTTCACCTGA[A/T]CATAAAAATCACCTG | 54455 |
rs371558457 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16293698 | AAGTTTTAGGGAAGC[A/G]AAATGCAGCTTCTTC | 54455 |
rs371560837 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16327805 | CCTCCAGGTTCAAGC[A/G]ATTCTCTCACCTCTG | 54455 |
rs371567397 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16301162 | CCTTGGCCTCCCAAA[A/G]TGTTGGGATTACAGG | 54455 |
rs371584155 | in-del | -/TGAGT | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16279348 | GGCAGGATGACTGCT[-/TGAGT]CTAGGAGTTTGAGGC | 54455 |
rs371607652 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16335056 | ACACAGCAAAACCTC[A/G]TCTGTACAAAAAAAA | 54455 |
rs371646834 | snp | C/T | 8.43917e-05 | 0.00649529 | intron-variant | FBXO42 | GRCh38.p7 | 1:16315453 | GTAATAGGTAAAACA[C/T]AAATATCAGTATTCC | 54455 |
rs371653101 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16323744 | GCAGTGAGCCGAGAT[C/T]GTACCACTGCACTCC | 54455 |
rs371654922 | in-del | -/AC | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16301686 | AAAAAAAAAAAAACA[-/AC]AAAAAAAAAAGAAAC | 54455 |
rs371716625 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16351122 | ATGATGTCATCATTC[C/T]TAAGCAGAAGTAAAG | 54455 |
rs371793455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16345093 | GACAGAGTGAGACTC[C/T]GTCTCAAAAAAACGA | 54455 |
rs371813336 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16334968 | GCAGTGGTTCACACC[C/T]GTAATCCCAGCACTG | 54455 |
rs371816102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16299353 | AAACCCAGCCAACAG[C/T]GGGGCCCTGAGGTCC | 54455 |
rs371836077 | in-del | -/TGAAAA | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16324131 | TTTTATCAACTCAAA[-/TGAAAA]AGTTATAGAAAGTAG | 54455 |
rs371861165 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16285092 | CGGAGGCTGCAGTGA[A/G]CCGAGATCGCACCCC | 54455 |
rs371930743 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | FBXO42 | GRCh38.p7 | 1:16325056 | CAGCCAAAGCAACAA[A/C]GTGAGACCCTGTCTC | 54455 |
rs371945502 | in-del | -/CC | | | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16353263 | AGCCCCCACCCCCCC[-/CC]CCCAACACCAAACCA | 54455 |
rs371977812 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16323739 | AGATTGCAGTGAGCC[A/G]AGATCGTACCACTGC | 54455 |
rs371977912 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16278199 | CCATCTCAACTAAAA[A/G]TACAAAATTAGCTGG | 54455 |
rs371985596 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16345717 | GCTGGGCATGGTGGC[A/G]GGCGCCTGTAGTCCC | 54455 |
rs371993352 | snp | C/T | 1.65509e-05 | 0.00287666 | intron-variant | FBXO42 | GRCh38.p7 | 1:16256801 | TAGCATTCAGGATCT[C/T]ACAACAATCCGTAGT | 54455 |
rs371995474 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16346612 | AGAATGGTGTGAACC[C/T]GGGAAGCAGAGCTTG | 54455 |
rs372020388 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16351367 | CAACGTCGGGGCCAG[A/C]AACTGCCAGCAAGTA | 54455 |
rs372024789 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16345553 | ACTGGCATTCCCTGT[-/A]AAAAGACACTGAGTC | 54455 |
rs372121193 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16301496 | GGCGAAACCCCGTCT[C/T]TACTAAAACTACAAA | 54455 |
rs372128277 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16260013 | GAAAGTTCTATTTAA[C/T]AGCGGTATTTTAGAA | 54455 |
rs372132800 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16340404 | GCTCACTGCAGCCTC[C/T]GCCTCTCCCAGGTTC | 54455 |
rs372133300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16301390 | CAAGAAGGCTGGGTG[C/T]GGTGGCTCACACCTG | 54455 |
rs372157411 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16309582 | GACTTTTTATACACA[A/G]TACCAAAGGCATGAT | 54455 |
rs372157513 | in-del | -/CAAA | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16323435 | AAACAAACAAACAAA[-/CAAA]AAAAGTAATTAAGGG | 54455 |
rs372160770 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16288160 | AACAATAATAATAGG[C/T]CGGGTGCAGTGGCTC | 54455 |
rs372201490 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16338025 | AGCACTTTGGGAGGC[C/T]GAGGCAGGTGGATCA | 54455 |
rs372205048 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16350394 | TGGTTCAGATTTACA[C/T]CTTTAGCAAAGACAC | 54455 |
rs372284171 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16254079 | GCAAAGTGTTATGCT[A/C]CTACTTAGCACTTAG | 54455 |
rs372307252 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16314413 | GCCAGATCGCCTGAA[C/T]GTGAATCTTTAATCC | 54455 |
rs372324727 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16313308 | AGAGAGAGAAAGAAA[C/G]AAAGAGAAAAGAAAA | 54455 |
rs372326677 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16307316 | CCAGCCCGGGCAACA[C/G/T]AGCAAGACCCCATTT | 54455 |
rs372330593 | snp | C/G/T | 0.000247162 | 0.0111144 | missense, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16256721 | GCAAGTCCTTGTACA[C/G/T]GACCAGAGTTGCTCC | 54455 |
rs372341955 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | FBXO42 | GRCh38.p7 | 1:16246677 | CCCGGCTAATTTTTG[C/T]ATTTTTAGTAGAGAC | 54455 |
rs372352870 | in-del | -/C | 0.104504 | 0.2033 | intron-variant | FBXO42 | GRCh38.p7 | 1:16274570 | ATAAGTAATGTATAT[-/C]CCCCCCCCATACAAA | 54455 |
rs372405053 | snp | A/C/T | 0.000712298 | 0.0188587 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251154 | GCTTCCAGACTCCGA[A/C/T]GCAGGGCACCTGGGG | 54455 |
rs372573582 | in-del | -/GA | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16281617 | TGGACTACAGGTATG[-/GA]TCACCATGCCTGGCT | 54455 |
rs372587405 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | FBXO42 | GRCh38.p7 | 1:16333445 | AGTGAGACCCCCCCC[C/G]CCCATTTCCAAGAAG | 54455 |
rs372591339 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16295727 | GACACACAATGAAAT[G/T]ATTTTAATCAATACT | 54455 |
rs372605574 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16335063 | AAAACCTCGTCTGTA[A/C]AAAAAAAAAAAAAAA | 54455 |
rs372656341 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16350749 | GAGAAACTGCAAAAA[A/G]AAAAAAAAAAAGAAA | 54455 |
rs372712759 | in-del | -/C | | | intron-variant, utr-variant-5-prime | FBXO42 | GRCh38.p7 | 1:16261151 | TCTTCAATCTTAATC[-/C]GGTAAAGCCAAAGAC | 54455 |
rs372790277 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16299152 | GAGTAGCTGGGATTA[C/T]AGGCATGTGCCACCA | 54455 |
rs372791251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16280602 | ACTGGGTGTCAGATA[C/T]ATGGAAACTCTCTCT | 54455 |
rs372804620 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | FBXO42 | GRCh38.p7 | 1:16346793 | AGAGTCTCACTCTGT[C/T]GCCCAGGCTGGAGGG | 54455 |
rs372820411 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16289596 | GCTCCTCTAACATGT[C/T]CTTTTCTTTGCTGCA | 54455 |
rs372879342 | snp | G/T | 8.26276e-05 | 0.00642705 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16253654 | GATTGGCCACCTCGA[G/T]GATGAGGACTGGGGC | 54455 |
rs372917127 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16342112 | CAAAACCCTAACTCT[A/G]CAGGCCAGGTGCAGT | 54455 |
rs372973617 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16275837 | AACATGGCAAAACCC[C/T]GTCTCTACTAAAAAA | 54455 |
rs373008846 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16247951 | CAAAAGGCACACTTG[C/T]AGGAATGGAAGGGGT | 54455 |
rs373013007 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | FBXO42 | GRCh38.p7 | 1:16352295 | GGGTTCGCTCCGCTG[A/G]CGACGGTAATGAGGG | 54455 |
rs373034537 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16268421 | AACTTTCTAAATAAA[C/T]AAGAAGGATTTCTTC | 54455 |
rs373038834 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16346007 | AAGGACACACTACCA[A/T]CTTAAGGAGGCTTAT | 54455 |
rs373089293 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16327015 | CCATCTCTCTCTATG[A/G]CCCACTTCTAAATGT | 54455 |
rs373137109 | in-del | -/TT | 0.0103295 | 0.0711199 | intron-variant | FBXO42 | GRCh38.p7 | 1:16302850 | ATCTCATGAAAATTC[-/TT]TCACTATAACAAGAA | 54455 |
rs373177507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16294178 | CTCAAATTGCCCTGC[C/T]TCATGAGTGCAAAAA | 54455 |
rs373188289 | snp | A/G | 3.29701e-05 | 0.00406005 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251717 | AGGTGATGGGCGAGA[A/G]TTCAAACTGGGGCTG | 54455 |
rs373198483 | snp | A/G | | | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16353118 | CAAGGGAGCAACCTG[A/G]TGTGTAGGTGAGAAC | 54455 |
rs373211019 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16338278 | AAAAAAAGAGGGAGG[A/G]TCGCTTGAGCACTGA | 54455 |
rs373231902 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16345756 | GGGAGGCTGAGGCAG[A/G]AGAATGGCATGAACC | 54455 |
rs373235471 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16316095 | GAATCACTTGAACCT[A/G]GGAGGCAGAGTTGCA | 54455 |
rs373242383 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16258022 | GTCCTGCAGCTTTAA[A/C/T]CAAAAAGAAAAAAAA | 54455 |
rs373245780 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16301523 | CAAAAATTAGCTGCG[C/T]GTGGTGGCAGGCACC | 54455 |
rs373256407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16330356 | ACTAGGCCCTGTTTC[C/T]ACAAAAAAAATTTAA | 54455 |
rs373323721 | snp | A/C | | | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16318098 | AAAAAATTTACTGAG[A/C]TGAATACTCACGCAC | 54455 |
rs373330379 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16339470 | GGTGCGTGCCACCAC[A/G]CCCAGCTAATTTTTG | 54455 |
rs373367533 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16283630 | GCCTCCCGAGTAGCT[A/G]GGATTACAGGCACCC | 54455 |
rs373389348 | snp | A/G | 3.30666e-05 | 0.00406598 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251071 | TCCCAGGAGAGCCTG[A/G]AGAAGACCCAAGAGG | 54455 |
rs373398613 | snp | C/T | 1.66239e-05 | 0.00288299 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16253726 | AGGACCCAGACATCA[C/T]TGCTCCTGTGAATTA | 54455 |
rs373421398 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16275685 | GTTCATCTCCTCAAG[A/G]GGGAATGAGAAATAG | 54455 |
rs373458104 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16278579 | GTCCCAGACTCCCTT[C/G]TTTAGACATTTCCTG | 54455 |
rs373469667 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16248634 | AAGGTACAGCAATAG[C/T]GGTAACACCTGAATT | 54455 |
rs373498921 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16278746 | CAGTAATATTCTGGA[C/T]AGTTATTTCTAGACA | 54455 |
rs373513903 | snp | A/G/T | 1.64868e-05 | 0.00287109 | missense, synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16252324 | CAGTTCTGGGGCCCC[A/G/T]TGCTCTTCATTTTCT | 54455 |
rs373514773 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16336561 | GGGGTTTCACCATGT[G/T]GGCCAGGCTGGTCTT | 54455 |
rs373550522 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16311087 | ATCCCAACACTTTGG[A/G]GAATGGCATGAACCC | 54455 |
rs373562877 | snp | A/G | 8.23988e-05 | 0.00641815 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251682 | GTTTCAGGAACGAGA[A/G]CTGGAGGAGTGGCAC | 54455 |
rs373650147 | snp | A/G | 0.000153988 | 0.00877328 | stop-gained, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16305878 | GAATGTTTCCTTCCT[A/G]GACAGCCTTCATGAA | 54455 |
rs373665910 | in-del | -/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16314923 | TACAATTAACCAGAT[-/C]AACTCTAAGAATATG | 54455 |
rs373697746 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16328101 | TTTTCTATAAAACTG[C/G]TAAGACTCAAAGCTC | 54455 |
rs373700566 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16281619 | GACTACAGGTATGGA[C/T]CACCATGCCTGGCTA | 54455 |
rs373727083 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16309128 | GCTGGAGTGCTGTGG[C/T]GCGATCTTGGCTTAC | 54455 |
rs373739577 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16350878 | GCCTATGGATCAATG[C/T]AGATTGAATCATCTA | 54455 |
rs373745175 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16281209 | TCAGGTGATCCGCCC[A/G]CCTCGGCCTCCCAAA | 54455 |
rs373750107 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16301042 | TAGCTGGATTACAGG[C/T]GTGCGCCCACCACGC | 54455 |
rs373755378 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16253016 | AATAGTCTTGTATAC[G/T]CCTAGAAAAGAAGAC | 54455 |
rs373764165 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16339878 | AGGATCACTTAGCCT[G/T]GGAAATCCAGGCTGC | 54455 |
rs373832699 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16305657 | AGGTGGAGGCTGTAG[C/T]AAGCTGTGATTATGC | 54455 |
rs373852536 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | FBXO42 | GRCh38.p7 | 1:16302236 | TTTTAGAGAACAGGA[C/G]ACTTTCAGTCCATTA | 54455 |
rs373918193 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | FBXO42 | GRCh38.p7 | 1:16252423 | TAAGAGAAAAAACCA[A/G]TAACAAGACTCAGGT | 54455 |
rs373958017 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16263028 | TCTATATCAAAGAAT[A/G]ACATTCTCTTTAGCC | 54455 |
rs373988257 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16293062 | TGGTATAAAGGGCTA[A/G]AAAAGGTTATTCTCC | 54455 |
rs373996431 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16280481 | TAATAATAACGTACC[-/A]ATATTGGTTTATCAT | 54455 |
rs373998485 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16265196 | CCTCCCAGTTTCAAC[A/G]GATTCTCCTGCCTCA | 54455 |
rs374015900 | snp | C/T | 4.94279e-05 | 0.00497107 | missense, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16315301 | TATTATGTCTAGTCT[C/T]CTCAGCCTCCAATAC | 54455 |
rs374043388 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | FBXO42 | GRCh38.p7 | 1:16255867 | AGTCAGCACCACACA[C/G]TTTATGTAAAAATAG | 54455 |
rs374159217 | snp | A/T | 1.64863e-05 | 0.00287104 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251265 | CCCCCAACTGTCCTA[A/T]TGTCCATGCCATCCA | 54455 |
rs374170707 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16332646 | CCAGAGTTCAAGTGA[G/T]TCTCCTGCCTCAAGC | 54455 |
rs374256105 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16352659 | CACCCGCCTTCGCCG[A/C]GTCTCTAGCGTCGAC | 54455 |
rs374282393 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16276493 | AGCACGAGCCATGAA[C/T]TGGTCCATGGCACTA | 54455 |
rs374293259 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16312507 | TCAGTGATTGCCAGT[A/G]GTTGGTGGAAGGAAA | 54455 |
rs374358874 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16263390 | CAAGCTTGCATTGAG[C/T]CAAGATCACGTCACT | 54455 |
rs374372541 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16296367 | AAGAAATTCACAGAT[C/T]CAGGCCAGGTGCAGT | 54455 |
rs374395016 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16329382 | TGAACTCAGGAGTTC[A/G]AGATCAGCCTGGGCA | 54455 |
rs374411159 | snp | A/G | 3.33406e-05 | 0.00408279 | intron-variant | FBXO42 | GRCh38.p7 | 1:16294760 | CCTGGTAAGGAGGCA[A/G]AGATCAGCATTTCAT | 54455 |
rs374415851 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16312260 | CCAGCTATTCTGGTG[A/G]CTGAGGAGGGAAGAT | 54455 |
rs374422224 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16331686 | TTGAACTAGGGAGGC[A/G]GAGGTTTCAGTGAGC | 54455 |
rs374441805 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16302713 | CGGGGTTTCACCATG[C/T]TGGCCAGGCTGGTTT | 54455 |
rs374444390 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16313993 | GAGTCTTGCTCTGTC[A/G]CCCAGGCTGGAGTCC | 54455 |
rs374458441 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16306826 | ACCTCTGCCTCCTGG[A/G]TAGCAGGCACTACAG | 54455 |
rs374520951 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16277780 | GCGTGGTGGCTCAGG[C/T]CTGTAATCCCAGCAC | 54455 |
rs374526603 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16313627 | GCAGTTTCAATACAG[C/T]TGGTTCTTAGCCCTC | 54455 |
rs374533206 | snp | A/G | | | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16354344 | AGGGTCTCACTCTTC[A/G]CCCAGGCTGGAGTGC | 54455 |
rs374534043 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16334397 | GAGATCGAGCCTGGG[C/T]GACAGAGTGAGACTC | 54455 |
rs374542026 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16256040 | CGGTCTGGAGGGAGA[C/G]AGATGAGAAAACGAT | 54455 |
rs374570352 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16289231 | ACACCCTAGTTCTAC[-/A]AAAAAAAAAAGAAAG | 54455 |
rs374610909 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16310902 | TTGCTTGAACCCAGA[A/C]GGTGGAGGTTGCAGT | 54455 |
rs374646864 | snp | G/T | 1.64977e-05 | 0.00287203 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251008 | CATCTCCTTGGGCAG[G/T]CCCTGGGCGAGGGAT | 54455 |
rs374649779 | in-del | -/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16306032 | AGTTTCTTTTTTTTT[-/T]CTTTTTTTGAGATGG | 54455 |
rs374651148 | snp | A/C/G | 4.94233e-05 | 0.00497087 | missense, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16315282 | GGCAGCTCCGACATG[A/C/G]ACCTATTATGTCTAG | 54455 |
rs374682975 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16301362 | ACTATGAACAAGGTG[C/T]TGTGAAACAGTACAA | 54455 |
rs374686297 | snp | A/C/T | 4.95694e-05 | 0.00497822 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16253657 | TGGCCACCTCGAGGA[A/C/T]GAGGACTGGGGCCAG | 54455 |
rs374698144 | snp | C/T | 0.000231088 | 0.0107467 | intron-variant | FBXO42 | GRCh38.p7 | 1:16305966 | GACACTTAACTTATC[C/T]ATCAAATTATTAAAA | 54455 |
rs374700496 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16340208 | ATTAAAAAAATTAAA[A/G]ATCACCTAGCAGGTA | 54455 |
rs374709544 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16273191 | ACAACCGGTAACCAG[A/C]AAGTGACAGGGCTCA | 54455 |
rs374718478 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16280199 | CATTATATCTCCACG[C/G]TCTTCTTCCCAAAAG | 54455 |
rs374845013 | snp | C/T | 0.00597247 | 0.0543191 | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16352529 | CGCGCGCACTCACGT[C/T]AGCGCGGCGGGATGG | 54455 |
rs374855609 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16305419 | TAATTAAAAGTCGGA[A/T]AAAATACATGCCTTG | 54455 |
rs374873818 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16312926 | CAGCCTCCCGAGTAG[C/T]TAGGACTACAGGCAC | 54455 |
rs374936312 | in-del | -/CACT | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16339344 | TTTGAGATGAAGTCT[-/CACT]GTGTTGCCAGGCTGG | 54455 |
rs374988190 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16283537 | CAGTCTCGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 54455 |
rs375012254 | snp | A/G | 6.59131e-05 | 0.0057404 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16256722 | CAAGTCCTTGTACAC[A/G]ACCAGAGTTGCTCCA | 54455 |
rs375026127 | snp | G/T | 5.05438e-05 | 0.00502686 | intron-variant | FBXO42 | GRCh38.p7 | 1:16294738 | AGTTTCCATGCCAAG[G/T]GAGTCACCTGGTAAG | 54455 |
rs375094488 | in-del | -/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16345866 | AAAAAAAAAAAAAAA[-/G]ACACCAGGTCTTCTT | 54455 |
rs375175513 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16257400 | GCAGACCTTCAAGGA[C/T]TGGTGTGAAGGAATT | 54455 |
rs375186793 | in-del | -/CTCTTCCCCTAGAGCC | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16264616 | TCTTCCCCTAGAGCC[-/CTCTTCCCCTAGAGCC]AGGAGTCACCCTCAT | 54455 |
rs375189717 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16295930 | GCATGCTGGTTGGAG[C/T]CGACTAGAAAACAGA | 54455 |
rs375190218 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16335394 | CCTCCTGTATTGGCA[G/T]CCAAAAGTGCTGGAA | 54455 |
rs375192825 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16248232 | GAGACAATCACCTTC[A/G]CTGTGTTGAATCACT | 54455 |
rs375250571 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16314647 | TTAATCCATTTGGGA[C/T]GCTGAGGCGGGCGGA | 54455 |
rs375256449 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16255379 | TCGATCTGTTGCCCA[G/T]GCTGGAATGCAATGG | 54455 |
rs375362790 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16262743 | CACTCCGGTTGCCCA[A/G]GCTAGAGTCTGGAGT | 54455 |
rs375363332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16254800 | TCTGGCTCCTGACTA[C/T]GGCTTGAGCTGTCCA | 54455 |
rs375369904 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16323907 | GTCATCCCACAGCAT[A/G]AGGGCTTCTGAGGCT | 54455 |
rs375376506 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16345819 | AGCCACTGCACTCCC[A/G]CCTGGGCGACAGAGC | 54455 |
rs375382825 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FBXO42 | GRCh38.p7 | 1:16345748 | AGCTACTCGGGAGGC[C/T]GAGGCAGGAGAATGG | 54455 |
rs375384598 | snp | G/T | 1.65419e-05 | 0.00287588 | intron-variant | FBXO42 | GRCh38.p7 | 1:16294779 | TCAGCATTTCATCTC[G/T]TACCTGAAGCCAAAG | 54455 |
rs375476950 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16267674 | TATTTTACTCCTCAA[G/T]TGTAAAAAGGCCAGA | 54455 |
rs375488565 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16337783 | CAGCTACTCGGGAGG[C/T]TGAGGCAGAAGAATT | 54455 |
rs375519070 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16292405 | AAGCAATCCTCCTGT[C/T]TCACCCTCCCAAGTA | 54455 |
rs375519856 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16266529 | CAGGCAGTATACCAG[A/T]CCTTCACACACAAAA | 54455 |
rs375525796 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16309634 | GGCATGGTAGCTCAC[A/G]CCTGTAATCCCAACA | 54455 |
rs375528405 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16330670 | AAATTGGCCAGGTGC[A/G]GTGGCTCACGCCTGT | 54455 |
rs375536503 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16347771 | GAGGCGGGCAGATCA[C/T]GAGGTCTGGAAATCG | 54455 |
rs375540368 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16272219 | CTAACAGCATGAAGT[C/G]TGGCCAGATGTCCAC | 54455 |
rs375541740 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16335941 | TTTTTAAATTTTGTT[G/T]TGTTTTTGAGATGGA | 54455 |
rs375545544 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16291003 | AGCAGTATTCTCTAT[C/G]AAGACTCTCCACTCC | 54455 |
rs375577254 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16278014 | GCCACTGTACTCCAG[C/T]CTGGGTGATGGAGTG | 54455 |
rs375601927 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | FBXO42 | GRCh38.p7 | 1:16282075 | ATGATAGCTGAGGAA[A/T]CCAGTTTAGCACATC | 54455 |
rs375610725 | snp | A/G | | | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16317124 | CGTCTCTACTAAAAA[A/G]TACAAAAATTAGGCC | 54455 |
rs375615656 | snp | A/G | | | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16317777 | AAAAAATAATTAACC[A/G]GGTGTGCTGGCACAC | 54455 |
rs375625217 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FBXO42 | GRCh38.p7 | 1:16331477 | AAGTAAAAACCGGCT[C/T]GGTGCGGTGGCTCAT | 54455 |
rs375694111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16303993 | TATTTTTAGCAGAGA[C/T]GGGGTTGTACCATGT | 54455 |
rs375695139 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16327023 | CTCTATGACCCACTT[C/G]TAAATGTCATTTTAA | 54455 |
rs375696089 | in-del | -/CCTGTAATCCCAACACTTTGGGAG | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16296414 | CCAACACTTTGGGAG[-/CCTGTAATCCCAACACTTTGGGAG]GCTGAGGCAGGCGGA | 54455 |
rs375702269 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16323727 | CCCAGGAGGCGGAGA[C/T]TGCAGTGAGCCGAGA | 54455 |
rs375706226 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16314207 | CACCTGCCTTGGCCT[C/T]GCAAAGTGCTGGGAT | 54455 |
rs375793475 | snp | A/C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16346459 | TTTGGGAGTCCGAGG[A/C/T]GGGCGGATCATGAGG | 54455 |
rs375840250 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16284348 | ACTCACCAGCACCTG[C/G]AATCACATATTCCCT | 54455 |
rs375853950 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16322604 | AATTTTAAAAACTAA[A/G]AAAAAAACTATGCTA | 54455 |
rs375869250 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16338792 | GGAATGGAACATTTT[A/T]TTTCCATTTGTCTTT | 54455 |
rs375955972 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16266555 | CAAAACTGGCCTTGA[A/G]GGCAAAGTAATGCCA | 54455 |
rs375969379 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16312047 | ACTAACAAAAAAAAA[-/A]GCTAAGAAATCATGA | 54455 |
rs376029455 | snp | C/T | 3.29533e-05 | 0.00405901 | missense, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16256681 | GGATAAGGGCTTGGC[C/T]GCGTCCAGCCACCAA | 54455 |
rs376112020 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16265308 | GTTGGTCAGGCTGGT[A/C]TCGAACTCCCAACCT | 54455 |
rs376114387 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250783 | CCCTGCCTTGTACCA[C/T]GGTATGCAGGCTGGT | 54455 |
rs376128070 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16275424 | GGAGTGCAAGACCAG[C/T]CTGGGCATTACAGTG | 54455 |
rs376146288 | snp | C/T | 3.30038e-05 | 0.00406212 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16252359 | TGAGTGGCTGCCAGG[C/T]CCAAGGACCAGAATG | 54455 |
rs376204385 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16309553 | AAAATCTAGAAGACC[C/T]TGACTTTGGGGATGA | 54455 |
rs376207072 | snp | A/C | 1.65138e-05 | 0.00287343 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251744 | GCTGAGTGGGGCTCT[A/C]CCACTAGGAGCCTGG | 54455 |
rs376245266 | snp | A/C | 3.29603e-05 | 0.00405944 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251683 | TTTCAGGAACGAGAG[A/C]TGGAGGAGTGGCACT | 54455 |
rs376247320 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16347744 | CCTGTAATCCCCACA[A/C]TTTGGGAGGCCGAGG | 54455 |
rs376256317 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16315581 | AATACCACTTGTGAG[C/T]CACCTTAATTCGACA | 54455 |
rs376285760 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16292128 | TTTAAACATTCAGGA[C/G]TTTGTATGTTTTGTC | 54455 |
rs376311149 | in-del | -/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16338377 | AAAAAAAAAAAAAAA[-/G]AATAACAATGTTGCA | 54455 |
rs376335971 | in-del | -/AAAAAAAATAT | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16311497 | TGTCTCAAAAAAAAA[-/AAAAAAAATAT]ATATATATATATATA | 54455 |
rs376391284 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16270753 | ACTTACCATGAGATA[C/T]ACACACACACACACA | 54455 |
rs376393251 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16332725 | TTTGTATTTTTAGTA[A/G]AGATACAGTTTCACC | 54455 |
rs376419524 | in-del | -/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16281472 | CTTTTTCTTTTTTTG[-/T]TTTTTTTTTTTTTTT | 54455 |
rs376491444 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16330104 | TATTATCACACAATG[A/T]AGCTAGACACTAAGC | 54455 |
rs376491739 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16286209 | AGTCCCTTGGTAATC[C/T]CATGCAGTCTCATAG | 54455 |
rs376503139 | snp | A/G | 1.67158e-05 | 0.00289096 | intron-variant | FBXO42 | GRCh38.p7 | 1:16253734 | GACATCATTGCTCCT[A/G]TGAATTAAGGACAGA | 54455 |
rs376513483 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | FBXO42 | GRCh38.p7 | 1:16315089 | TACATTTAAGGGAGG[-/A]AAAAAACTAAATTTG | 54455 |
rs376513689 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16285214 | CCACTTAGCACCTCA[C/G]CTCCTTGCTCTCCTT | 54455 |
rs376557710 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16298767 | CGCTCGCCTCGGCCT[C/G]CCAAAGTGCTGAGAT | 54455 |
rs376610570 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16306143 | TCTCCTGCTTCAGCC[C/T]CCCGAGTAGCTGGGA | 54455 |
rs376611139 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16304696 | GCAGAGGGCTGGGCG[C/T]GGTGGCTCACACCTG | 54455 |
rs376616549 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16302159 | AGAGCTTAATATCTA[C/T]GGCGAGGAATCTGAG | 54455 |
rs376636575 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FBXO42 | GRCh38.p7 | 1:16341425 | ACCAACATGGTAAAA[C/T]ACCGTCTCTACTGAA | 54455 |
rs376680683 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16339359 | CACTGTGTTGCCAGG[C/T]TGGAATGCAGTGGCA | 54455 |
rs376694077 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16254213 | TGCCTAATGAGATTA[-/T]TTTTTTAACCATCTA | 54455 |
rs376716640 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16269628 | CCTCCCAGGTTCAAG[C/T]GATTTTCCTGCCTCA | 54455 |
rs376758502 | snp | C/T | 1.84817e-05 | 0.00303982 | intron-variant | FBXO42 | GRCh38.p7 | 1:16255836 | CCTAATGTAAAAAGA[C/T]AGGAGGAAGTCAAGA | 54455 |
rs376779272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16272448 | ATTTTAAGTAGAGAC[C/T]GGGTTTCACCATGTT | 54455 |
rs376854339 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | FBXO42 | GRCh38.p7 | 1:16261886 | ATTTTTTTTATTGTT[A/G]TATTTTTAGTAGAGG | 54455 |
rs376869025 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16290509 | CCAGCCTGGCCAACA[C/T]GGTGAAACTCCGTCT | 54455 |
rs376874391 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16327733 | TTTAAGACGGAGTCT[C/T]GCTCTGTTGCCCAGG | 54455 |
rs376909425 | in-del | -/C | | | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16353257 | AAAACTAAGCCCCCA[-/C]CCCCCCCCCAACACC | 54455 |
rs376912380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16260565 | TAATTTAATCCTTCT[A/G]AAATTCCTAGTTTTA | 54455 |
rs376919009 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16278245 | CCTGTAATCCCAGCT[A/G]CTCGGGAGGCTGAGG | 54455 |
rs376964053 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16344177 | TAATTTTGTATTTTT[A/G]GTAGAGATGGGGTTT | 54455 |
rs376967856 | snp | A/G | 1.6477e-05 | 0.00287024 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251334 | AGATCTATGGATCCT[A/G]ATCTCAGATCTTTCT | 54455 |
rs377054341 | in-del | -/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16304113 | CCAGCCAAATTTGTA[-/T]TTTTTTTTTTTTTTT | 54455 |
rs377071986 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16281083 | TTCTCCTGCCTCAGC[C/T]TCCCGAGTAGCTGGG | 54455 |
rs377108727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16276583 | GGGATAGTATCTTGC[A/G]TTCCTCTCCCATTTA | 54455 |
rs377117212 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16312696 | TTTCAGTATAGGTTC[A/G]TCAATTTTAACACAT | 54455 |
rs377147322 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16352807 | GCAGAGAGGGCTGTG[A/G]CGGATGTGAGTGCTC | 54455 |
rs377160714 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16320360 | GAGCAAACTCCATGT[A/C]AAAAAAAAAAAAAAA | 54455 |
rs377166307 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | FBXO42 | GRCh38.p7 | 1:16299879 | CAATCTCTTGATCTC[A/G]TGATTCACCTGCCTT | 54455 |
rs377237177 | snp | C/G | 0.000798403 | 0.0199641 | downstream-variant-500B | FBXO42 | GRCh38.p7 | 1:16246667 | TGCCACCATGCCCGG[C/G]TAATTTTTGTATTTT | 54455 |
rs377237385 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16289851 | AGGCAGGAGGTCGAG[A/G]CTACAGGGAGCTGTG | 54455 |
rs377286694 | snp | A/T | | | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16353976 | TTTATTTATTTATTT[A/T]CTTATTTTTATTTAT | 54455 |
rs377288826 | snp | C/T | 0.000285266 | 0.0119395 | intron-variant | FBXO42 | GRCh38.p7 | 1:16294953 | TAACTGCTGTGAAAA[C/T]TCTGAGGCCCTTCCA | 54455 |
rs377307476 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16288883 | GAATTGCTTGAACCC[A/G]GGAGGCAGAGGCTGT | 54455 |
rs377314532 | snp | A/G | 1.6554e-05 | 0.00287693 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16253713 | CTGCTCAAGGTCAAG[A/G]ACCCAGACATCATTG | 54455 |
rs377372153 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FBXO42 | GRCh38.p7 | 1:16262767 | CTGGAGTGCAGTGGC[A/G]TAATCGATCTCAGCT | 54455 |
rs377375923 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16300043 | AGGGGCAGGGGCAGG[C/G]AGGAAGACCCAACAA | 54455 |
rs377402068 | in-del | -/CAAAA | | | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16353239 | CAAAACAAAACAAAA[-/CAAAA]AACTAAGCCCCCACC | 54455 |
rs377429495 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | FBXO42 | GRCh38.p7 | 1:16275838 | ACATGGCAAAACCCC[A/G]TCTCTACTAAAAAAA | 54455 |
rs377495136 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16339557 | ACCTCATGATCAGCC[C/T]GCCTCAGCCATCCAA | 54455 |
rs377510855 | in-del | -/TAGCCT | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16257802 | TTCCTGCCTTAGCCT[-/TAGCCT]CCTGAGTAGCTGGGA | 54455 |
rs377554905 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16257051 | GTACCTATCTCATAA[A/G]GCTGTTTTGAGTATT | 54455 |
rs377600753 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16326146 | CTGCAACCTCCACCT[C/T]CTGAGTTCAAGCGAT | 54455 |
rs377606263 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16249576 | TTTGGAAGTAAAAAG[A/C]AGCCCATAGGGAAAA | 54455 |
rs377628469 | in-del | -/TTTAT | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16306488 | TCTAGTCCCTTTTAT[-/TTTAT]CTCATAAGGCAACAT | 54455 |
rs377630527 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16291024 | TCTCCACTCCCAACC[A/G]AAAGTGTTCCACTCC | 54455 |
rs377635127 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16347787 | GAGGTCTGGAAATCG[A/T]GACAATCCTGGCTAA | 54455 |
rs377735200 | in-del | -/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16344507 | TTTTTTTTTTTTTTT[-/G]TATTTTTTAGTAGAG | 54455 |
rs377749902 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16350410 | CTTTAGCAAAGACAC[C/T]AAGAAAATCGACAAA | 54455 |
rs377759556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16276109 | AAACTTGGCAGGGTG[C/T]GGTGGCTCACGCCTG | 54455 |
rs377761717 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | FBXO42 | GRCh38.p7 | 1:16312316 | GCAGTGAGCCAAAAT[C/T]GCACCAATGCACTCC | 54455 |
rs386366299 | in-del | -/GAA | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16270714 | AAGAAAAGAAAGAAG[-/GAA]AAAAGATAAATTCCA | 54455 |
rs386366300 | in-del | -/TTT | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16283495 | CTAACTGTGGCAAGT[-/TTT]TTTTTTTTTTTTTTT | 54455 |
rs386366301 | in-del | -/T | 0.5 | 0 | intron-variant | FBXO42 | GRCh38.p7 | 1:16289645 | ACTTCCCTCCACTAT[-/T]CATTCTTTAGGTCTC | 54455 |
rs386628908 | in-del | AGA/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16270706 | AAAAAAGAAAAGAAA[AGA/G]AAGAAGAAAAGATAA | 54455 |
rs386628909 | multinucleotide-polymorphism | CTC/TTT | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16277139 | CAATGAGATCAATCA[CTC/TTT]GTTTTTAAGACAGAA | 54455 |
rs386628910 | multinucleotide-polymorphism | AG/GC | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16298636 | TGCCTCAGCCTCCCA[AG/GC]TAGCTGGAATTACAG | 54455 |
rs386628911 | in-del | CA/TGCG | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16347153 | ATCTGTGTGTGTGTG[CA/TGCG]CATCAAAGCATCACA | 54455 |
rs386628912 | in-del | GT/TAC/TACAGCACAAGTAC | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16348327 | AACTACAGCACTAAG[GT/TAC/TACAGCACAAGTAC]AAATAACTTGTACTG | 54455 |
rs397702501 | in-del | -/A | 0.5 | 0 | intron-variant | FBXO42 | GRCh38.p7 | 1:16342598 | AAAAAAAAAAAAAAA[-/A]GTTATAGTAATACCA | 54455 |
rs397718869 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16343396 | AAAAACACAAAAAAA[-/A]TTAGCCTGGCATGGT | 54455 |
rs397815155 | in-del | -/C | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16247547 | TTTTCTTTCTTCCTC[-/C]TCCTCCTCCTCTTTT | 54455 |
rs397825151 | in-del | -/A | 0.375 | 0.216506 | intron-variant | FBXO42 | GRCh38.p7 | 1:16258376 | GCAAGACCCTGTCTC[-/A]AAAAAAAAAAAAGGA | 54455 |
rs397860543 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16326684 | ACCAAACCCTGTCTC[-/A]AAAAAAAAAAAAAAA | 54455 |
rs397949989 | in-del | -/T | | | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16318435 | TAAATAAATAAAGTT[-/T]GCCAAAATAAGCCAT | 54455 |
rs397979349 | in-del | -/T | 0 | 0 | intron-variant | FBXO42 | GRCh38.p7 | 1:16265795 | AGGCCTTGAAATGTC[-/T]TTTTTTTTTTTTTTA | 54455 |
rs397979350 | in-del | -/A | 0 | 0 | intron-variant | FBXO42 | GRCh38.p7 | 1:16282233 | GTCTCAAAAAAAAGA[-/A]AAAAAAAAAAAAGAA | 54455 |
rs397979352 | in-del | -/A | 0 | 0 | intron-variant | FBXO42 | GRCh38.p7 | 1:16312812 | CAGAGATTCTGTCTC[-/A]AAAAAAAAAAAAAGC | 54455 |
rs397979353 | in-del | -/T | 0 | 0 | intron-variant | FBXO42 | GRCh38.p7 | 1:16337916 | TTTGGCCTATTATTC[-/T]TTTTTTTTTTTTTTT | 54455 |
rs398049137 | in-del | -/T | 0.5 | 0 | intron-variant | FBXO42 | GRCh38.p7 | 1:16255352 | CTTTTTTTTTTTTTT[-/T]CCTTAAGAGTCTCGA | 54455 |
rs398049138 | in-del | -/A | 0.5 | 0 | intron-variant | FBXO42 | GRCh38.p7 | 1:16256542 | CTTGACACAAAAAAA[-/A]CAAAGAATCCACTGA | 54455 |
rs398102474 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16263744 | AAAAACAAAAAAAAA[-/A]CCGAAAAACCAAAAA | 54455 |
rs527251461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16322068 | CCAGCTACCTGGGAC[A/G]TGTAAAAAAAATTAC | 54455 |
rs527254701 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16329553 | CGCACCACTGCACTC[C/T]AGCCTGGGAGACAGA | 54455 |
rs527263176 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16332601 | GCTGGAGTGCAGTGG[C/T]ACAACCTCAGCTCAC | 54455 |
rs527333300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16329034 | TGGCCATGGTGGCGG[A/G]TGCCTGTAATCCCAG | 54455 |
rs527334983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16335771 | ACTAAGGAGGCTGAG[A/G]CAGGAGAATCGCTTG | 54455 |
rs527472537 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16301492 | ATAGGGCGAAACCCC[A/G]TCTCTACTAAAACTA | 54455 |
rs527475077 | in-del | -/ATAT | 0.0205511 | 0.0992634 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250474 | AGAGTTGGCTATATA[-/ATAT]ATATATATATATATA | 54455 |
rs527491305 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16257050 | AGTACCTATCTCATA[A/C]GGCTGTTTTGAGTAT | 54455 |
rs527511415 | in-del | -/C | 0.00279162 | 0.0372561 | intron-variant, utr-variant-5-prime | FBXO42 | GRCh38.p7 | 1:16261150 | TTCTTCAATCTTAAT[-/C]CGGTAAAGCCAAAGA | 54455 |
rs527519564 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16348657 | AGTGAGCAGAGATTG[A/C]GCCACTGCACTCCAG | 54455 |
rs527522673 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16301052 | ACAGGCGTGCGCCCA[A/C]CACGCCCAGCTAATT | 54455 |
rs527556143 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16286060 | AGCTAATTTTTTTTT[A/T]AATTTTTTGAGGAGA | 54455 |
rs527678016 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16296107 | AGTCTAGAAAAGATG[A/C]ATGAGTGCTAAGTTC | 54455 |
rs527685281 | snp | A/G | 4.94474e-05 | 0.00497205 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250700 | TACAAAGTACAAGGC[A/G]TTTGTTTTTGGATAG | 54455 |
rs527696154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16343877 | CTAGCTACTCGGGAG[A/G]CTGAGGCAGGAGGAT | 54455 |
rs527754112 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16288521 | AGATACTACTACTTA[A/C]ACATTTAATAGGAAC | 54455 |
rs527787944 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16296813 | CTGGCACTAGTTACC[C/T]GAGTTCAGAAAAAGG | 54455 |
rs527926538 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16316063 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 54455 |
rs527932939 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16350780 | GAAAGAAAGAAAGAA[A/G]GAAAGAAAGAAAGAA | 54455 |
rs527972873 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | FBXO42 | GRCh38.p7 | 1:16258686 | GAATACTTTCATAAA[A/T]AAAACCAACACTAAT | 54455 |
rs527988444 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16336681 | TTTAATTTGGACATA[G/T]TCATAGAAGAAGGAT | 54455 |
rs527997018 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16339543 | GTCTTGATGTCTTGA[C/T]CTCATGATCAGCCCG | 54455 |
rs527999009 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16308459 | GTGAACAGCCATTGA[A/C]TTTCAGCCTGGGAAA | 54455 |
rs528007730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16309729 | AAGGAGACCCTGTCT[C/T]GACAAAGTATTTTTT | 54455 |
rs528010091 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16258093 | ACTACATTAACCTGA[C/G]AGCAGTCGAGATGCT | 54455 |
rs528013020 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16265350 | CCCGTCTTGGCCCCC[C/G]AAAGTGCTGGGATTA | 54455 |
rs528094873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16267130 | TATTTGGAATGGTCT[C/T]CAAAATACTGCAGCC | 54455 |
rs528143177 | in-del | -/A | 0.424968 | 0.178567 | intron-variant | FBXO42 | GRCh38.p7 | 1:16342581 | TTGAGATCCTGTCTC[-/A]AAAAAAAAAAAAAAA | 54455 |
rs528144315 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16297750 | CAGGCGCCTGTAGTT[A/C]CAGTTACTCAGGAGG | 54455 |
rs528179945 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16304092 | TTAGAGGCGTGAGCC[A/C]CAGCACCCAGCCAAA | 54455 |
rs528193123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16252772 | AACTCTGACAGTTAT[C/T]AACCTGCTTTTTTGT | 54455 |
rs528212239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16260489 | GCTAGGATTACAGGT[A/G]TGAGCCACCGCGCCT | 54455 |
rs528305348 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16324147 | GAAAAAGTTATAGAA[A/C]GTAGAAAAAGGATAA | 54455 |
rs528326558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16274652 | GCTAGAGTGCAGTGG[C/T]GTGAACTTGGCTCAC | 54455 |
rs528333654 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | FBXO42 | GRCh38.p7 | 1:16347151 | TTATCTGTGTGTGTG[A/T]GTGCGCATCAAAGCA | 54455 |
rs528345356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16266362 | CAGTGGCATGTACCT[A/G]TAGTCCCCAGCTACT | 54455 |
rs528349902 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16349673 | CAAGACCAGCCTGGC[C/T]AACATAGTGAAACCT | 54455 |
rs528370357 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16326205 | GGATTACAGGCATGC[A/G]CCAGCATGCCCGGCT | 54455 |
rs528405158 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16321935 | GCAATTTGGGAGTCC[A/G]AGGTGGGTGGATCAC | 54455 |
rs528411874 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-5-prime | FBXO42 | GRCh38.p7 | 1:16352335 | CAGGGCCAGAGCAGA[A/G]GCGCTCTGCCTCAGG | 54455 |
rs528414197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16274061 | CAAGAACACAGAACT[A/G]TACTTTGGGAATCTG | 54455 |
rs528432007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16325976 | CAGCAAAATGCTTTA[C/T]TTGGTAGAAAGGTAA | 54455 |
rs528470331 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16283529 | TTTTGAGACAGTCTC[A/G]CTCTGTCGCCCAGGC | 54455 |
rs528477361 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16275563 | ATTTGAGGCTGCAGT[A/G]AGCTATGATGATGCC | 54455 |
rs528570694 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16263835 | TTTTTTTGGAGGCAG[A/T]GTTTCACTCTTTTCG | 54455 |
rs528601498 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16319701 | GCGGATCACGAGCTC[C/G]GGAGTTCGAGACCAG | 54455 |
rs528642457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16276052 | ATCACAGCTCTTACC[C/T]ACCTAGGAACAGCAC | 54455 |
rs528655091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16298244 | AAACAAAAACAAAAA[C/T]ACCAAAGAACTACAA | 54455 |
rs528693280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16338485 | TCCCCCTGCTTTGAT[A/G]CTGGGCATTGTCATC | 54455 |
rs528708026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16253543 | TTTGGCTTAGTGCAT[A/G]TTGGCATCTTACCTG | 54455 |
rs528746111 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16332334 | GCACATTGTTATTAT[C/T]ACCATTGCTATAGTT | 54455 |
rs528749636 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16282767 | GGGCAGATCACCTGA[A/G]GTCAGGAGTTCGAGA | 54455 |
rs528831667 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16279947 | TGCCTCCCTGGCTCA[A/G]CTGATTCTTGTGCCT | 54455 |
rs528852800 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16341380 | GCCGAGGCGGGCAGA[G/T]CATGAGGTCAGGAGT | 54455 |
rs528854010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16333570 | CTCCAGCCTGTGACA[A/G]TGCAAGACGATCTCT | 54455 |
rs528865551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16292105 | GAGACATTTTGTTAG[A/G]AAATTACTTTAAACA | 54455 |
rs528890326 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FBXO42 | GRCh38.p7 | 1:16340643 | CTGAGGGTTAGGGTT[C/T]TGCCATGCCAAGGTT | 54455 |
rs528983540 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16310120 | GAATGGCGTGAACCC[A/G]GGAGAGGAGCTTGCA | 54455 |
rs529053058 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16304439 | TTGAATTTTATAATC[A/G]ACACTTGTCACATTC | 54455 |
rs529055893 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16314035 | CTTGGCTCACTGCAA[C/T]CTCTGCCTCCTGGGT | 54455 |
rs529096150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16305695 | CTCCAGCTTGGGTGA[C/T]AGAGTGAGACCTTGT | 54455 |
rs529100886 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16262101 | TAAATTATTGCTACT[A/T]TAAGAATTGATATTG | 54455 |
rs529137930 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16334951 | TTTAATAATGGCCAC[A/G]CGCAGTGGTTCACAC | 54455 |
rs529144460 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16278132 | GAGGCCGAGGCGGGC[A/G]GATCACCTGAGGCTG | 54455 |
rs529167733 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16346669 | CTCCAGCCTGGGCGA[C/T]AGAGCTAGACTCCGT | 54455 |
rs529187826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16255234 | ATAGAGCAAATTTTT[C/T]AATTTATTGGTCTGT | 54455 |
rs529189486 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16332140 | CTTCTGATACAGCAT[A/G]TGTTTTGTTCATTCT | 54455 |
rs529212729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16306540 | TATTTACTCCAAAGC[A/G]AAGGTGTTGGGGGAT | 54455 |
rs529276488 | in-del | -/T | 0.396546 | 0.202545 | intron-variant | FBXO42 | GRCh38.p7 | 1:16346754 | GTACTGAACAGTACA[-/T]TTTTTTTTTTTTTTT | 54455 |
rs529277927 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16345949 | ATAGCTTGTTGTGAC[-/A]AAAAAATAAGGAAGC | 54455 |
rs529283206 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16308266 | AATTACAGGCGTGAG[A/C]CACTGTGTCCAGCCT | 54455 |
rs529306993 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16307529 | AAAAACAAGCAAAAA[A/T]AAAAAAGACGAACAT | 54455 |
rs529325975 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16351615 | ATCGTTTTCTCTTCG[C/T]TTACAAATTCGTTCC | 54455 |
rs529355546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16301603 | GGGAGGCAGAGGCTG[C/T]AGTGAGCCAAGACCG | 54455 |
rs529363291 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16342058 | GAGGTGGGTGGATCA[C/G]CTGAGCCCAGGGGTT | 54455 |
rs529403859 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16248664 | TGCTAGCCTTCTGGC[C/T]CAGCTTTCCCTTGTA | 54455 |
rs529423996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16257084 | ATAGTATATTCAAAG[C/T]ACCTAACATAATGCC | 54455 |
rs529424811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16348763 | CGGTCAGCTTCAATC[A/G]AAAAGGAATTAAGAT | 54455 |
rs529448442 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16308587 | TCACCACAATCTCTG[C/T]CTCCTGAGCACAAGG | 54455 |
rs529448583 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16341768 | CTGAGGTCAGGAGTT[C/T]GAGACCAACCTGACC | 54455 |
rs529461500 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16339358 | TCACTGTGTTGCCAG[A/G]CTGGAATGCAGTGGC | 54455 |
rs529465546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16321452 | TTTCACACGTAAGCA[C/T]ACTAACTCAATGAAT | 54455 |
rs529503182 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FBXO42 | GRCh38.p7 | 1:16271425 | AGCTGGGATTACAGG[C/T]GCCTGCCACCACACC | 54455 |
rs529552513 | snp | C/T | | | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16317286 | AGCTGGGCGTGGTAG[C/T]GTATGCCTGCAGTCC | 54455 |
rs529556127 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16328187 | AATTTTTAAAAAAAA[A/C]CACTTACTCAGGAGG | 54455 |
rs529566021 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16265661 | TGAAAACTAAAAAAG[-/A]AAAAAAAAAAGGCAA | 54455 |
rs529568411 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16287691 | CCTGGCCTCAAGCCA[C/T]CCTCCCACTCAGCCT | 54455 |
rs529584170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16314847 | CGAGATTGCGCCACT[A/G]CACTCCAGCCTGGGC | 54455 |
rs529675118 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16280187 | TGATGAGAATGGCAT[G/T]ATATCTCCACGGTCT | 54455 |
rs529687633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16322996 | TTTGGTTTCTATTCA[A/G]CTAGACATCTGACAA | 54455 |
rs529763180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16316707 | GCCACTGCACTCCAG[C/T]CTGGGACACAGAGAA | 54455 |
rs529805506 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16265537 | ATCTAATTTAATCAT[G/T]ATAACCTTAAAATGC | 54455 |
rs529843303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16273134 | AACTATGAAAGGTAG[A/G]TATTACCATCTCTAC | 54455 |
rs529856265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16335388 | AGTGATCCTCCTGTA[C/T]TGGCATCCAAAAGTG | 54455 |
rs529866659 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16335829 | CTGAGATCACGCCAT[C/T]GCATTCCAGCCTGGG | 54455 |
rs529922007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16329676 | AAAAAAAGGCTGGGT[A/G]CGGTGGCTTATGCCT | 54455 |
rs529953187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16279141 | TTTTTAAGGATATCC[C/T]GTGGTCTTCCTACTG | 54455 |
rs530002799 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16280798 | AAACAAAAGAAAAGA[A/G]GAACGAAAACTACTC | 54455 |
rs530006565 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16299420 | CAATTGGCATTTTCC[G/T]GCTTCTCTTGAGCAA | 54455 |
rs530011933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16337962 | CTACACTTTGGGAGG[C/T]CAAGGAGGGAGGATT | 54455 |
rs530046754 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | FBXO42 | GRCh38.p7 | 1:16286850 | AGAGTCATCTTGATT[C/G]CTTTCTTTCTCTTTC | 54455 |
rs530072077 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16331068 | GAGGTTGCAGTGAGC[A/C]AAGACAGCGCCACTG | 54455 |
rs530093725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16288756 | TGAGGTCAAGGGTTC[C/T]AGACCAGCCTGGGCA | 54455 |
rs530093763 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | FBXO42 | GRCh38.p7 | 1:16281723 | GAGTGCAGTGGCAAT[A/C]TTGGCTCACTGTAAC | 54455 |
rs530197465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16324033 | CTCTTGAAAATATAC[C/T]GTTGAATGAGAGATT | 54455 |
rs530203892 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16273628 | GCTTATGCCTGTAAT[C/T]GTAGCACTTTGGAGG | 54455 |
rs530206188 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16248711 | GATCGAACAGTCTTT[A/G]CCAAGCAAGGATTGG | 54455 |
rs530229986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16310269 | GGGAGGTGGAAGCAG[A/G]AGAATTCCTTGAACC | 54455 |
rs530253442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16281305 | AATTATAGTATCATC[C/T]TATTGAGTTGATATG | 54455 |
rs530263128 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16350882 | ATGGATCAATGTAGA[G/T]TGAATCATCTATTTA | 54455 |
rs530306404 | snp | A/G | 1.65655e-05 | 0.00287793 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251510 | ACTCCCACCATTGAG[A/G]ATAGGAGAGCCGTCT | 54455 |
rs530307883 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16321549 | GCTTCCCCAACGTGA[C/T]TGAATGAATGTACTG | 54455 |
rs530321973 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16344566 | GTGTCAAACTCCCAA[A/C]CTCAGGTGATCTGCC | 54455 |
rs530338549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16303319 | AACAGGAGCTCTTAT[C/T]ATTTGGGGCAGGATA | 54455 |
rs530343012 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16333148 | TAAGTATTCCTCTGA[A/C]CTTCTATTCATTTTG | 54455 |
rs530347388 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | FBXO42 | GRCh38.p7 | 1:16336065 | GCCTCAGCCTCCTAA[A/G]TTGCTGGGATTACAG | 54455 |
rs530357034 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16343901 | GGAGGATCGCTTGAG[C/G]CAGGAGATTGGGGCT | 54455 |
rs530370127 | in-del | -/GTGATGTTTTT | 0.00398564 | 0.0444627 | intron-variant | FBXO42 | GRCh38.p7 | 1:16326733 | AGTTAATTCTGATAG[-/GTGATGTTTTT]TCTAGGATTTATAAG | 54455 |
rs530389910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16297068 | CTCAGTCTCCCGAGT[A/G]GGTGTAACTGGGATT | 54455 |
rs530447348 | in-del | -/A | 0.0209421 | 0.100162 | intron-variant | FBXO42 | GRCh38.p7 | 1:16340960 | CCAAAATTTATTTAT[-/A]AAAAAATCAGCAGTA | 54455 |
rs530456992 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16353193 | GATACAGAGTCAAAG[C/G]CTTCAGTCTAAACTC | 54455 |
rs530532293 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16298503 | AGAAATTAGCAATGT[A/C]CTATGAGTTATTTAT | 54455 |
rs530557536 | in-del | -/A | 0.299452 | 0.248938 | intron-variant | FBXO42 | GRCh38.p7 | 1:16256535 | AGGGACTCTTGACAC[-/A]AAAAAAACAAAGAAT | 54455 |
rs530578804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16346410 | AGAAAATAAGAGAGC[A/G]AGGCGTAGTGGCTCA | 54455 |
rs530651610 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16346037 | TGCTGGCCAAATTTC[A/T]GGGTCAGAACGACTA | 54455 |
rs530766307 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16313078 | GGGATTACAGGCGTG[C/T]TCCACTGTGTCCGCT | 54455 |
rs530771737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16324799 | CTAGCCTGGGTGACA[C/T]AGCAAGACTCCGTTT | 54455 |
rs530831036 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16332466 | AGCAAATAAAGTTAT[A/C]CTCCTGGAGGTTGGA | 54455 |
rs530849684 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16346721 | ACAAGAGAAAATAAG[A/T]TACTAAGCTAAATTA | 54455 |
rs530898618 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16321399 | TTTTGAAACTCTGAG[C/T]TTTTCTTGTTTTCAT | 54455 |
rs530942256 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16269079 | CTTCCAAAGTACTGG[G/T]ATTACAGGCGTGAGC | 54455 |
rs531035727 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16323942 | GGACAAAGCAGCAAC[C/T]CTGAACAGATGTCAT | 54455 |
rs531052508 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16269867 | TGTTTTGTTTTGTTT[C/T]GTTTTGTTTTTGAGA | 54455 |
rs531061523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16276110 | AACTTGGCAGGGTGC[A/G]GTGGCTCACGCCTGT | 54455 |
rs531061809 | in-del | -/CGC | 0.00159617 | 0.0282053 | utr-variant-5-prime | FBXO42 | GRCh38.p7 | 1:16352429 | CTTCCTCCACTCAAA[-/CGC]CGCCGCCGCCGCCGC | 54455 |
rs531089947 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16326158 | CCTCCTGAGTTCAAG[C/T]GATTCTCCTGCCTCA | 54455 |
rs531149281 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16283567 | CAGTGGCACAATCTT[A/G]GCTCACTGCAACCTC | 54455 |
rs531212444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16334372 | CGGGAGGCGGAGCTT[A/G]CAGTGAGCGGAGATC | 54455 |
rs531357280 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16246897 | CATCAGGGGAAAACA[A/T]TAACAAAAAATGAAA | 54455 |
rs531372846 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | FBXO42 | GRCh38.p7 | 1:16246685 | ATTTTTGTATTTTTA[C/G]TAGAGACAGGGTTTC | 54455 |
rs531415669 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16328956 | AATCACAAGGTCAGG[A/G]GTTCGAGACAAGCCT | 54455 |
rs531472366 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16286011 | CCTGCATCAGCCTTC[C/T]GAGCAGCTGGGACTA | 54455 |
rs531480345 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16276748 | GGATACCTGAGAATA[A/G]GAGAAACAATGCTAG | 54455 |
rs531493460 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16341503 | TACTCAGGAGGCTGA[C/G]GCAGGAGAATCGCTT | 54455 |
rs531523163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16347988 | CAGACCCGAGACTCC[A/G]TCTCAAAAAAAAAAA | 54455 |
rs531543115 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16304697 | CAGAGGGCTGGGCGC[A/G]GTGGCTCACACCTGT | 54455 |
rs531611439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16293047 | GCACTAAGTGCAATA[C/T]GGTATAAAGGGCTAG | 54455 |
rs531612535 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16248699 | AGGACCCCACATGAT[C/T]GAACAGTCTTTGCCA | 54455 |
rs531674212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16295895 | CATTAAGTCCCAATA[C/T]GTATCCAAGAGCTAC | 54455 |
rs531731331 | snp | A/C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16269231 | TAGCTGGGACTACAG[A/C/G]CACATGATATCATAC | 54455 |
rs531758906 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16308900 | AGGCATGTGCCACCA[C/T]GCCTAGCTAATTTTG | 54455 |
rs531767089 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16349770 | AGGAAGCTGAGGCAG[C/G]AGAATCGCCTGAACC | 54455 |
rs531832804 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | FBXO42 | GRCh38.p7 | 1:16335886 | AAAAAAAAAAAAAAA[A/C]CTTTTGACTGTTTTA | 54455 |
rs531832839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16343684 | AAAAATTAGCCAGGC[A/G]TGGTGGTGGGTGCCT | 54455 |
rs531874932 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16257194 | AAGAATGTAGAGGAC[A/C]AGGGAGAAGTATACA | 54455 |
rs531885828 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16278802 | TTGAGACGGAGTTTC[A/G]CTCTTGTTGCCGAGG | 54455 |
rs531896398 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16314020 | GTCCAGTGGCGTGAT[C/G]TTGGCTCACTGCAAC | 54455 |
rs531904934 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16284573 | GTGGCAGCTCATGCC[C/T]ATAATCCCAGCACTT | 54455 |
rs531908718 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16263927 | GCGATTCTCCTGGCT[C/G]AGCCTCCCGAGTAGC | 54455 |
rs531911406 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16348840 | CCACCTATAATCAAC[A/T]TTGTAAGGAATAACA | 54455 |
rs531964912 | in-del | -/A | 0.131038 | 0.219882 | intron-variant | FBXO42 | GRCh38.p7 | 1:16297867 | GTGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 54455 |
rs531985018 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16321990 | CCTAGCCAACATGGC[A/G]AAACCCTGTCTCTAC | 54455 |
rs532031543 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16311432 | AGTCAAGGCCGCAAT[C/G]AGCTATGACCATGCC | 54455 |
rs532048008 | snp | C/T | | | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16352991 | GAGTCACACACCTAT[C/T]AGTGGAGGTGGGGCG | 54455 |
rs532054206 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16323728 | CCAGGAGGCGGAGAT[C/T]GCAGTGAGCCGAGAT | 54455 |
rs532055387 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16315830 | AGGAAAAACTAACTC[C/T]GGGTCTTGCAAAAAG | 54455 |
rs532057037 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16281406 | CGTACATCTCCTGGG[A/G]CAGTATGCCACTCAT | 54455 |
rs532059205 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16315962 | GATCACCTGAAGTTG[G/T]GAGTTTGAGACCAGC | 54455 |
rs532091359 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16319739 | AATATGGTGAAACTC[C/T]GTCTCTACTAAAAAT | 54455 |
rs532135575 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16266329 | CCATGCTAAAATAAG[C/T]TTGCTAACAGCTAGG | 54455 |
rs532154018 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16349649 | GTGGATCGCCTGCGG[A/T]CAGGAGTTCAAGACC | 54455 |
rs532207829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16329880 | CTTGAACCAAGGAGG[C/T]AGAGGTTGGAGTGAG | 54455 |
rs532233690 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16351888 | GGGCACCCGACCCCC[C/G]ACTCCTCTCTCGCAA | 54455 |
rs532273586 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16258911 | TCCAGCTAATTTTTA[A/T]AATTTTTTTGTTGTG | 54455 |
rs532297540 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | FBXO42 | GRCh38.p7 | 1:16330402 | GGTGGCAGCTACTTG[C/G]GGGCTGGGGTGGAAG | 54455 |
rs532349143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16336512 | ACAGGCAGACACCAT[C/T]ACGCCTGGCTAAGTT | 54455 |
rs532374875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16331583 | AACATGGTGAAACCC[C/T]GTCTCTGCTAAAAAT | 54455 |
rs532412154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16323412 | GACAGTGCGAGACTC[C/T]GTCTCAAAAACAAAC | 54455 |
rs532444708 | in-del | -/AG | 0.00279162 | 0.0372561 | intron-variant | FBXO42 | GRCh38.p7 | 1:16324311 | GCTTAGATCCCACAC[-/AG]GGTACAAAAAGAAGA | 54455 |
rs532459275 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16295862 | TCCCAAAGCAACAGA[A/T]TGAAAAAGCATGGAA | 54455 |
rs532459317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16327357 | TTTTTCTTCACTGAC[A/G]AATTAACTGAAATAA | 54455 |
rs532476722 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FBXO42 | GRCh38.p7 | 1:16325418 | ACCAAAAAAAAAGCC[C/T]AGAAATAGAATAATT | 54455 |
rs532485527 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16280261 | TCCAAGTTGAAGAGT[A/G]GTCTATAAGATACCT | 54455 |
rs532502274 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16324906 | TTAAACATTGTCAAA[A/T]TATTGTAACTTAAAC | 54455 |
rs532535106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16281953 | CCTCAAGTGATCCTC[A/G]ACTCCCAAAGTGCTG | 54455 |
rs532537527 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16290502 | TTCAAGACCAGCCTG[C/G]CCAACATGGTGAAAC | 54455 |
rs532618650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16318189 | TTTGGGAGGCCTAGG[C/T]GGGTGGATCACCTGA | 54455 |
rs532633005 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16352495 | GAGCGCGCATGCGCC[A/G]GGGCGGGCGCGGCGG | 54455 |
rs532655964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16338091 | AGTGAAACCCCGTCT[C/T]CACTAAAAATACAAA | 54455 |
rs532697403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16297713 | TAAACATACAAAAAA[A/G]AAAATTAGCCGGGCG | 54455 |
rs532720144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16345189 | AGCACTTTGGGAGAC[C/T]AAGGCAGGCGGATCA | 54455 |
rs532729785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16297164 | GGCCAAGCTGGTCTC[A/G]AACTCCTGACCTCAG | 54455 |
rs532744461 | snp | A/G/T | 6.61927e-05 | 0.00575262 | stop-gained, missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251562 | CCTTCCCGGGAACCT[A/G/T]AAGGAGTCTGCCTTT | 54455 |
rs532753341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16344640 | AGCACCCATCCAGTT[A/G]TTACATTTTTAAACC | 54455 |
rs532768493 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16303393 | CACATCCCTGCCCCT[C/T]GCCTACTTCATGTTT | 54455 |
rs532836516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16283784 | ACAGGTGTGAGCCAC[C/T]GTGCCTGGCCTGTGG | 54455 |
rs532894482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16291417 | AGACAGTCTCACTCC[A/G]CCACCCAGGCTGGGG | 54455 |
rs532906728 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | FBXO42 | GRCh38.p7 | 1:16273023 | GACAACTTACTCCTT[A/G]GCTAGTATCTCCGTA | 54455 |
rs532928307 | in-del | -/TTAATACAGTA | 0.00676609 | 0.0577691 | intron-variant | FBXO42 | GRCh38.p7 | 1:16283964 | CAGTATGACTTACGT[-/TTAATACAGTA]TGACTCTGTATTAAA | 54455 |
rs532931152 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16340007 | ACAGTGAAACCCTGT[C/G]TCTACTAAAAATACA | 54455 |
rs532971914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16298602 | GCAACCTCCGCCTCC[C/T]AGGTTCAAGTGATTC | 54455 |
rs532986792 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16305678 | GTGATTATGCCACTG[C/T]ACTCCAGCTTGGGTG | 54455 |
rs532995798 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16343737 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCCAGGAG | 54455 |
rs533004439 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FBXO42 | GRCh38.p7 | 1:16268105 | AATCTGATAATTTGT[C/T]AATTGCAGTTCTAAT | 54455 |
rs533009848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16292028 | TCAAAAAGCTCAGGT[C/T]TTCCTCCTTCTAAAA | 54455 |
rs533017082 | in-del | -/C | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16247687 | AGTAAGCCCAGTATG[-/C]CCCTAAAATGAAATT | 54455 |
rs533026944 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16281025 | GGAGTGCAATGACAC[A/G]ATTCTCAGCTCACCG | 54455 |
rs533053874 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16262011 | GCCACCGCGCCTGGC[A/C]CAGGTATATCAAATT | 54455 |
rs533111248 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16314811 | ATAACATGACCCCGG[C/G]AGGCAGAGCTTGCAG | 54455 |
rs533116598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16312297 | AGCCCGGGAGACGGA[A/G]GTTGCAGTGAGCCAA | 54455 |
rs533127576 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16320866 | CTAAATTCACCAAGG[A/C]AAAGAGCCCAAAGAA | 54455 |
rs533133464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16348421 | TTAGTGTAATTCGTC[A/G]GGAGCGGTGGCTGAA | 54455 |
rs533175675 | in-del | -/A | 0.0111196 | 0.0737302 | intron-variant | FBXO42 | GRCh38.p7 | 1:16278369 | CTCAAAAAAAAAAAC[-/A]AAAAAACAAAACAAA | 54455 |
rs533190882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16262773 | TGCAGTGGCGTAATC[A/G]ATCTCAGCTCACTGC | 54455 |
rs533195456 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16314024 | AGTGGCGTGATCTTG[C/G]CTCACTGCAACCTCT | 54455 |
rs533204112 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16346105 | AATCCATGTACAATA[C/T]AGTGATACAGAAAGT | 54455 |
rs533266346 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | FBXO42 | GRCh38.p7 | 1:16307476 | ATGCCATGCCACTGC[A/C]CTCCAGCCTGGGCAA | 54455 |
rs533282878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16305027 | ATATATTTAGGCTGA[C/T]ACTTTTCCCTAATTC | 54455 |
rs533291964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16268793 | ACATGGAGAAACCCC[A/G]TCTCTACTAAAAACG | 54455 |
rs533325413 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16288206 | GGAGGCCGAGGCAGA[C/T]GGATCACGAGGTCAA | 54455 |
rs533409826 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16331754 | CTCAAAATAAATAAA[C/T]AAATAAATAAATGCA | 54455 |
rs533436311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16320599 | ACCTCTGCCTCCCAG[A/G]TTCAAGTGATTCTCC | 54455 |
rs533494243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16276629 | AACTACATTTAGGAC[A/G]TAAAGTTAATCTATA | 54455 |
rs533497020 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16259770 | GACTCTGTCTCAAAA[A/G]AAAAAAAAAAGAAAG | 54455 |
rs533547281 | in-del | -/T | 0.0111196 | 0.0737302 | intron-variant | FBXO42 | GRCh38.p7 | 1:16274588 | CAAATTATGCCCCCG[-/T]TTTTTTTTTTTTTTT | 54455 |
rs533596927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16314552 | CAATAGTGCTTGACA[C/T]GTGATAAAAGCTATG | 54455 |
rs533604479 | snp | C/T | 1.648e-05 | 0.0028705 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16256731 | GTACACGACCAGAGT[C/T]GCTCCAGCTTTGGGG | 54455 |
rs533609095 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16264044 | TCGAACTCCTGGCCT[C/G]AGGTGATCCACCTGC | 54455 |
rs533639675 | in-del | -/AAAAC | 0.00318978 | 0.0398085 | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16353220 | ACTCTGTAAGCCAAA[-/AAAAC]AAAACAAAACAAAAC | 54455 |
rs533642791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16348473 | GGAGGCAAAGGTGGG[C/T]GGATCACATGGTCAG | 54455 |
rs533671669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16315593 | GAGCCACCTTAATTC[A/G]ACAGGTACAGCTCAA | 54455 |
rs533713365 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant | FBXO42 | GRCh38.p7 | 1:16334436 | AAAAAAAAAAAAAAA[A/C]AAAACAGACTGATTC | 54455 |
rs533740019 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16315030 | AACCAGGGTAAGAAA[C/G]AAAACCGGGTAGTAT | 54455 |
rs533747787 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16333952 | AGGAAAATTGATTTT[C/G]CATACTGTATCAACT | 54455 |
rs533749996 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16267808 | AAAACATCATTCTAT[C/G]GGTCATTTATGAAAT | 54455 |
rs533832117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16321585 | TGAACTCCCTGGAGG[C/T]AGGACCATTGGCCTA | 54455 |
rs533832272 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16321198 | AAACATCAAACCCCA[C/T]ACCTTTGAGGGCATG | 54455 |
rs533970959 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16284708 | CGCAGGGACTCATGC[A/C]TGTAATTCCAGCACT | 54455 |
rs533974277 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16304226 | GGTTCAAGCAGTTCT[C/G]CTGTCTCAGCCTCCC | 54455 |
rs534088154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16285457 | TTTTGTATTTTTAGT[A/G]GAGACGGGGTTTCAC | 54455 |
rs534144411 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | FBXO42 | GRCh38.p7 | 1:16282970 | TGGGTGACAGAGTGA[C/G]ACTCCGTCTCAAAAA | 54455 |
rs534149076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16257455 | CAAACACCATCTAGA[C/T]TGGACCTCTGGGCTA | 54455 |
rs534234798 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16259718 | TTGCAGTGAGCCGAG[A/G]TTGAGCCACTGCACT | 54455 |
rs534256817 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16248750 | CCAGAGCCTGAGTCG[C/T]GAAAGGGAAGTGTGG | 54455 |
rs534310928 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16331575 | GCCTGGCCAACATGG[A/T]GAAACCCTGTCTCTG | 54455 |
rs534350541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16303024 | CAGGGGTTCGAGACC[A/G]GTCTGGACAACATGG | 54455 |
rs534388242 | snp | A/C | 0.0248432 | 0.108648 | intron-variant | FBXO42 | GRCh38.p7 | 1:16301693 | AAAAAACAACAAAAA[A/C]AAAAGAAACGGTACA | 54455 |
rs534388789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16289043 | GGCCTTCTGTCTAGT[C/T]TGGTTTACTTTCTTG | 54455 |
rs534389391 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250215 | ACAGCACCTGAAGCA[C/T]GAGAGTCTAAAACCC | 54455 |
rs534416469 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FBXO42 | GRCh38.p7 | 1:16337662 | CCAAGGTGGGCGGAT[C/T]ACCTGAGGTCAGGAG | 54455 |
rs534419453 | in-del | -/G | 0.00358779 | 0.0422022 | intron-variant | FBXO42 | GRCh38.p7 | 1:16266088 | ACTTTCAAATAAAAT[-/G]AATCAAACAAGATAG | 54455 |
rs534426336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16297254 | CAGCCCCCCACCTTC[C/T]TTTATTTTCCCTTAA | 54455 |
rs534433786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16349084 | TGCAGAAGCCATAAC[C/T]GGGGCATACTGTGTG | 54455 |
rs534468444 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16309304 | GGATGGTCTCAATCT[C/T]TTGACCTCATGATCC | 54455 |
rs534469636 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16284211 | AGACTACAATGTACA[C/T]AATTATACATTCACA | 54455 |
rs534478269 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16258227 | TCAAGGTTGAGAAGG[C/T]AGAGCAGAGGACTGT | 54455 |
rs534488238 | in-del | -/T | 0.281841 | 0.247964 | intron-variant | FBXO42 | GRCh38.p7 | 1:16320661 | ACTATGCCCAGCTAA[-/T]TTTTTTTTTTTTTTG | 54455 |
rs534492454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16335574 | AATCTGGATCAAAAA[C/T]TTTTGACTGGGCCAG | 54455 |
rs534494172 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16273527 | AAACAATGTTGATGG[A/C]AGCTATATTCAAAGT | 54455 |
rs534535365 | in-del | -/AAT | 0.306377 | 0.24356 | intron-variant | FBXO42 | GRCh38.p7 | 1:16331426 | TCTCAAAAAGAAAAT[-/AAT]AATAATAATAATAAT | 54455 |
rs534542699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16342260 | AATTAGCCGGGTGTG[A/G]TGGCACATGCCTGTA | 54455 |
rs534573984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16258982 | TGGCCTCAAGCGATC[C/T]TCCCGCCTCAGCCTC | 54455 |
rs534608068 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | FBXO42 | GRCh38.p7 | 1:16296558 | AGGAGGCTGAGGCAG[C/G]AGAATCGCTTGAACC | 54455 |
rs534619751 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16289220 | GGCAACATAGTGACA[C/T]CCTAGTTCTACAAAA | 54455 |
rs534623223 | snp | A/G | 1.65553e-05 | 0.00287705 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251184 | GAGACGGCCCCTGCA[A/G]GGGCACTGGCCACGT | 54455 |
rs534671556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16311639 | GCTCCATATCATTTG[C/T]CATCAGGGAAATGCA | 54455 |
rs534727249 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16344524 | ATTTTTTAGTAGAGA[C/T]GGGGTTTCCCCATGT | 54455 |
rs534746714 | snp | A/G | 1.64819e-05 | 0.00287066 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251678 | TCGGGTTTCAGGAAC[A/G]AGAGCTGGAGGAGTG | 54455 |
rs534747618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16336879 | AATTCTAGCTACTTG[A/G]GAGGCTGAGGCAGGA | 54455 |
rs534782544 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16253195 | ACCTACAAAGACACA[C/G]GTTTCTGACTTTCTA | 54455 |
rs534787962 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16261375 | GCTTTCCAAAACGAC[A/G]TCTCAGATATCTTGA | 54455 |
rs534800172 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16352745 | CGGTGGTTTGAGACT[A/G]ACATTTAGCCAGGAA | 54455 |
rs534800649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16264978 | TTTCCCACAATTGTA[A/G]TGTCTATTTACACAG | 54455 |
rs534861773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | FBXO42 | GRCh38.p7 | 1:16316508 | TGGGATTCTGAGGCC[A/G]GCAGATCACCTTAGG | 54455 |
rs534894558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16331219 | GAGTTCAAGACCATC[C/T]TGGCTAACACGGTGA | 54455 |
rs534967937 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16324978 | TGCAGTGGCTCACAC[C/T]AGTAAACCCAACACT | 54455 |
rs534992890 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16338607 | GAATTTACTAAATGT[A/G]AGCAGACCAGTAGCA | 54455 |
rs535004785 | snp | C/T | | | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16354073 | GCTCACTGCAACTTC[C/T]GCCTCCTGGGTTCAA | 54455 |
rs535063465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16275898 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGGAG | 54455 |
rs535076838 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16261714 | TATCAATTTTTTTTT[G/T]TTGTTTTTGAGACGC | 54455 |
rs535134255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16269378 | ACAGGTATAAACCAC[C/T]GAACCCAGACTTTTT | 54455 |
rs535211309 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16281429 | CCACTCATGACTAAC[C/T]GGGTTTGTAAAAGGT | 54455 |
rs535215932 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16276316 | ACCCAGGAGGCAGAG[C/T]TTGCAGTAAGCCGAG | 54455 |
rs535289474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16253947 | TGAATCCCAGCTCTG[C/T]AGCCTGAACAAGTCA | 54455 |
rs535290312 | snp | C/G/T | 0.00199529 | 0.0315338 | intron-variant | FBXO42 | GRCh38.p7 | 1:16274899 | CCAGCTATCAAATTA[C/G/T]GTCTTAATAGAATAA | 54455 |
rs535297486 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16346174 | TCACCAATTCTTTAC[A/G]AAGAAATTTATAATG | 54455 |
rs535354398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16283039 | CCTGAGATTAGGTGA[A/G]TCTGCTATGGGGCCA | 54455 |
rs535373512 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16265124 | TTGAGACGGAGTTTC[A/G]CTCTTGTTGCCCAGG | 54455 |
rs535381358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16274322 | CAAAAAACACAAAAA[A/G]AAAAGAAAAGAAAAG | 54455 |
rs535383189 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16282076 | TGATAGCTGAGGAAT[A/C]CAGTTTAGCACATCA | 54455 |
rs535408037 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16283923 | TACTTGAAAACTTCT[A/T]TCTTGATTTAAAGTA | 54455 |
rs535413361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16326366 | CAGCCTCTTTATTGT[C/T]AATACAACTACTCGA | 54455 |
rs535422366 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16299731 | CTCACTGCAACCTCC[A/G]CCTCCTGGGTTCAAG | 54455 |
rs535425057 | in-del | -/A | | | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16317559 | AAGACTGGCCACTGC[-/A]ACTCCAGCCTAGACA | 54455 |
rs535438619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16333117 | TCTTCTTGAGGTTCT[A/G]TCCCCTCCAGCCAAT | 54455 |
rs535455672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16292617 | GCAGTCTTTAAACTT[A/G]ATGGTTTAAAAAAAA | 54455 |
rs535455743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16301074 | CAGCTAATTTTTGTA[C/T]GTTTAGTGGAGATAG | 54455 |
rs535513988 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16282163 | GACTGCAAGAAGATA[A/T]CATAGGGCTCCAGGA | 54455 |
rs535563310 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16293351 | GTCTCGAACTCCTGA[C/T]CTCAGGTGATCCGCC | 54455 |
rs535605179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16334005 | TCAGAAACTTCAAAA[A/G]GCTATATTCTGTACC | 54455 |
rs535617969 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | FBXO42 | GRCh38.p7 | 1:16337345 | CTAGATGAGAAAATG[C/G]AATCAACAGGTATTG | 54455 |
rs535641879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16298770 | TCGCCTCGGCCTCCC[A/G]AAGTGCTGAGATTAT | 54455 |
rs535654739 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16292308 | CTCTTTTCTTCCCTT[C/T]CTCTCTTTCTCTTTC | 54455 |
rs535680289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16305251 | AAATTAGCCAGGCGT[A/G]GTGGCATGCACCTGT | 54455 |
rs535682263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16298081 | AATACAAAAATTGGT[C/T]TGGCATGGTGGCATG | 54455 |
rs535707434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16291597 | ATGTTGGCCAGGCTC[A/G]TCTGGAACTCCTGGC | 54455 |
rs535722308 | snp | A/G | 0.089084 | 0.191327 | intron-variant | FBXO42 | GRCh38.p7 | 1:16313370 | AGAAAGAAAGAAAGA[A/G]AGAGAAAAGAAAGAA | 54455 |
rs535727004 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16253051 | GAAACAGGTTTTGAA[A/C]ACTTAGTAGCATGCA | 54455 |
rs535734889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16340035 | ACAAAAAATTAGCCA[A/G]GCGTGGTGGCAGGCG | 54455 |
rs535797887 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16254767 | CCGCTGAATCAGACA[A/G]TGATACAGATGGAAT | 54455 |
rs535850933 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16246959 | TTTCATTCCTACACT[C/G]TTATGTGCCCAAAAT | 54455 |
rs535882677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16348327 | AACTACAGCACTAAG[A/G]TAAATAACTTGTACT | 54455 |
rs535898541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16309022 | TGCTGGGATTACAGG[C/T]GTGAGCCACCATGCC | 54455 |
rs535908565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16285535 | CCTTGGCCTCCCAAA[A/G]TACTGGGATTACAGG | 54455 |
rs535938718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16350166 | AACTAAGGTAAGGAA[C/T]TGCAAAGGTCAAAAT | 54455 |
rs535953676 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16258102 | ACCTGACAGCAGTCG[A/C]GATGCTCCAATCTAG | 54455 |
rs535972527 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16278840 | CTGGAATGTAATGGC[A/G]CAATCTTGGCTCACC | 54455 |
rs535972904 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16343632 | TTCAAGACCAGCCTC[A/G]CCAAGATGGTGAAAC | 54455 |
rs535986361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16309170 | ACTCCCAGATTCAAG[C/T]GATTCTCCTGCCTCA | 54455 |
rs536029698 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16354287 | TTCTGGGATTACAGG[C/T]GTGAGCCACGGCGCC | 54455 |
rs536042521 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16328542 | GTGATAATGGATTAG[A/C]GTGGGAGACAGGATG | 54455 |
rs536100793 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16321025 | GTTTATTTACATTAC[G/T]ATTTTTCCCAATCAG | 54455 |
rs536136712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16255562 | CTGGTCACAAACTCC[C/T]GACCTCAGGTGATCC | 54455 |
rs536149820 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16248700 | GGACCCCACATGATC[A/G]AACAGTCTTTGCCAA | 54455 |
rs536164340 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16253549 | TTAGTGCATATTGGC[A/G]TCTTACCTGACTCCC | 54455 |
rs536171294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16306808 | GGCTCAAGCAATACT[C/T]CTACCTCTGCCTCCT | 54455 |
rs536173456 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16262833 | TCACACCTCAGCCTC[A/C]CAAGTAGCTGGGACT | 54455 |
rs536194838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16278433 | CGACGTTTGGGACCT[A/G]AGCCAAAGGATGGAC | 54455 |
rs536229631 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16280699 | AGGATCACCTGAACC[A/C]CGGAGGTCAAGGCTG | 54455 |
rs536253772 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16330596 | GGCAGATCACAAGGT[A/C]AACAGATTGAGACCA | 54455 |
rs536280773 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16296155 | ATCCTTTGGAAATGA[C/T]GATCACATTCCTTAC | 54455 |
rs536292016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16315706 | TCGTAAACCAGAAAA[C/T]TTGTTCTCCAACAAT | 54455 |
rs536297465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16265885 | GTTGGCTCTGAGTAC[A/G]GGTGTCTTAGGCAAT | 54455 |
rs536372068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16257495 | AATTCTGAAAAAAAA[C/T]ACTTTGGCTTATGCT | 54455 |
rs536378535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16301750 | TATCTTCAAGTAGAC[A/G]ACAATCTTGTGGGGG | 54455 |
rs536423311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16277997 | CAGTAAACCATGTTC[A/G]TGCCACTGTACTCCA | 54455 |
rs536446896 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250076 | ATGTGGAATAAAATC[A/C]TTTGTTGGGTAACTT | 54455 |
rs536505234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16271846 | CATTGGATGCTCAAT[A/G]GTCCTCTGTAGGCTG | 54455 |
rs536507055 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16263743 | AAAAAAACAAAAAAA[A/C]ACCGAAAAACCAAAA | 54455 |
rs536509595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16287960 | AAATAGCCTGGCCAA[C/T]GTGATGAAACCCTGT | 54455 |
rs536547595 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16264281 | TAGCACCTGAGTAAC[C/T]GGAAATCTTGAACAA | 54455 |
rs536559749 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16267546 | GGAGCTGAGATCAGG[G/T]TCGGCTCCAGCTACT | 54455 |
rs536587946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16270945 | AAGTGCCAAGGGGGG[A/G]AAAAAAAAACAAAAC | 54455 |
rs536615905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16323552 | CTGTAATCCCAGCAC[C/T]TTGGGAGGCTGAGGT | 54455 |
rs536634316 | in-del | -/AATC | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16329585 | GAGACTCCATCTATA[-/AATC]AATCAATCAATCAAT | 54455 |
rs536651677 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16323222 | AGGAGTTTGAGACCA[G/T]CCTGGCCAACATGGT | 54455 |
rs536720835 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16317110 | ACATGGTGAAACTCC[A/G]TCTCTACTAAAAAAT | 54455 |
rs536732253 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | FBXO42 | GRCh38.p7 | 1:16261743 | GCGTCTCACTCTGTC[G/T]CTCAGGCTGGAGTGC | 54455 |
rs536760211 | in-del | -/AA | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16342416 | AAAAAAAAAAAAAAA[-/AA]CCCTAACTCTACAGA | 54455 |
rs536798244 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16310546 | CTCCCCAAAATAACT[A/G]ATAAGCCAGAATTCA | 54455 |
rs536884032 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16294396 | AGCTGGCAACAACAA[A/C]AGATATTCAGAGACC | 54455 |
rs536884162 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | FBXO42 | GRCh38.p7 | 1:16302411 | CACAGTTCCACATGG[C/G]TGGAGAGGCCTCAGG | 54455 |
rs536904510 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16331358 | AGGCAGAGCTTGCAG[A/T]GAGCCGAGATCGTGC | 54455 |
rs536916723 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16279525 | TTTAAAAGCAAATCA[A/T]GTTGATATCTAAAAA | 54455 |
rs536961087 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | FBXO42 | GRCh38.p7 | 1:16316542 | GGAGTTCGAGACCAG[C/T]GTGGGCAACATGGCG | 54455 |
rs536977507 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16259688 | CAAGAATTGCTTGAA[A/G]CTAGGAGGTGGAGGT | 54455 |
rs537059666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16345452 | ATAAAATAAAATAAA[A/G]TTTTCTAGTTGTGAC | 54455 |
rs537066214 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16337729 | CCTCTACAAAAAATA[C/G]AAAAATTAGCTGGGC | 54455 |
rs537087436 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16312453 | ATTCCAACTATATGA[A/C]CTTCTAGAAAAGGCA | 54455 |
rs537147103 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16288882 | AGAATTGCTTGAACC[C/T]GGGAGGCAGAGGCTG | 54455 |
rs537159713 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16257969 | TACAGGCGTGAGCCA[C/T]CATGCCTCGCTGAGA | 54455 |
rs537178083 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16330634 | CAACATGGTGAAACC[C/T]TGTCTCTACTAAAAA | 54455 |
rs537212492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16318368 | CGTTGCAGTGAGCTG[A/G]GGTCGCTCCACTGCA | 54455 |
rs537252948 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16325064 | GCAACAAAGTGAGAC[C/G]CTGTCTCTATAAAAA | 54455 |
rs537270245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16259064 | CTCTAGGAAGAGTTA[C/T]CACATCAATCTGAAG | 54455 |
rs537282778 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16317670 | GGCTCATGCCTATAA[A/T]CCCAACACTTTAGTA | 54455 |
rs537291328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16310051 | ATAGAAAAAATTAGC[C/T]GGGTGTGGTGGTGGA | 54455 |
rs537295181 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16344821 | AATATTTTCTGGGCC[A/G]GGCGTGGTGGCTCAC | 54455 |
rs537375015 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16321041 | ATTTTTCCCAATCAG[A/G]ATAAATTTGATTCAA | 54455 |
rs537381863 | snp | C/G | 1.64833e-05 | 0.00287078 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251275 | TCCTATTGTCCATGC[C/G]ATCCATGGGATTACT | 54455 |
rs537447737 | in-del | -/AAAC | 0.00517822 | 0.0506191 | intron-variant | FBXO42 | GRCh38.p7 | 1:16347514 | AGAGACTTCCTCTCA[-/AAAC]AAACAAACAAACAAA | 54455 |
rs537547178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16254455 | ATCAAGGACAGACTG[A/G]CATCTCTAACCCTCA | 54455 |
rs537556072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16298818 | CCCGGCCAATGTCCT[A/G]TGACTTCTGAAACCT | 54455 |
rs537620342 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16325653 | CCCATCAATATACTT[C/T]CTTTTTTTTGTTGTT | 54455 |
rs537725182 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16311891 | AGGAGCTGAAAACTT[A/T]TGTCCACAGAAACAC | 54455 |
rs537738603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16326730 | TTGAGTTAATTCTGA[C/T]AGGTGATGTTTTTTC | 54455 |
rs537795756 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16268436 | CAAGAAGGATTTCTT[A/C]CTTTTCTAAGGGAAC | 54455 |
rs537809678 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16321182 | GTTACACCCTCCACA[A/G]AAACATCAAACCCCA | 54455 |
rs537824760 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16277012 | TTTTCAACATGGAGG[A/G]GAAATAGCTAAGGAC | 54455 |
rs537841187 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16320148 | GCAGATCACCTGAGG[C/T]CAGGAGTTCAAGACC | 54455 |
rs537853839 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16327464 | AAAAAGTAAAACAAA[A/G]CAAAAATGCTAACTT | 54455 |
rs537876824 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16293407 | ATTACAGGCGTGAGC[C/G]AGTGGGCCTGGCTTG | 54455 |
rs537906528 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16282540 | CATTTTCTCTTTTAA[-/A]AAAAAAAAAAATGCT | 54455 |
rs537961203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16286241 | TTTAAATCCATCTGG[A/G]TTAGTCTATTCTCAC | 54455 |
rs537984953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16270147 | AGGTGTGAGCCACCA[C/T]GCCCAGCCACTTTCT | 54455 |
rs538030256 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16347725 | GCAGGCACAGTGGCT[C/T]ACGCCTGTAATCCCC | 54455 |
rs538064098 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16263496 | GCCGGCCAGGCGTGG[G/T]GGATCACCTGAGGTC | 54455 |
rs538073966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16291167 | GTGCCCTCCCCTCAG[C/T]CACCCTCCAATCTAC | 54455 |
rs538112538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16284693 | AAAAATTAGGCCAGG[C/T]GCAGGGACTCATGCC | 54455 |
rs538132547 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16333887 | TTAAAGGGATGGAAT[C/G]CAGAAAACTAATTTC | 54455 |
rs538149284 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16283951 | GTAACCGAAAAAGGC[A/C]GTATGACTTACGTTG | 54455 |
rs538177401 | snp | C/T | 1.66454e-05 | 0.00288486 | intron-variant | FBXO42 | GRCh38.p7 | 1:16256565 | TCCACTGATTTAAGG[C/T]CTTTTCTTCCAGATT | 54455 |
rs538256589 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16334770 | CCCAAATAGGAGAAA[C/T]GCTAAATAGAAAGTA | 54455 |
rs538256675 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16342145 | CTCACGCCTGTAATC[C/T]CAGCACTTTGGGAGG | 54455 |
rs538279189 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16275967 | GACCCCGTCTCAAAA[C/T]AAATAAACAAAAAAG | 54455 |
rs538288698 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16334219 | CGGGCAGATCATGAG[A/G]TCAGGAGATCGAGAC | 54455 |
rs538311526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16278694 | TGACAGCCCCATATG[C/T]AACCTTTTTAAGGTA | 54455 |
rs538369286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16335532 | ATCTATTCTTTATTT[C/T]GCTGTAGTATTAAAC | 54455 |
rs538369989 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16303012 | ACTGCTTGAGCTCAG[A/G]GGTTCGAGACCAGTC | 54455 |
rs538383807 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16343363 | AGCGTGGGCAACATG[A/G]CAAAACTCCATCTCT | 54455 |
rs538386919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16307670 | TGAAATTAAAACACA[C/T]AATTTGAAATTAAAA | 54455 |
rs538417879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16323122 | CACAAATTCAAAAGG[C/T]TAAAAAATGTAATTG | 54455 |
rs538419371 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | FBXO42 | GRCh38.p7 | 1:16280776 | AAACCCAGTCTCCAG[-/A]AAAAAAAAACAAAAG | 54455 |
rs538478799 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FBXO42 | GRCh38.p7 | 1:16314983 | ATGCAAATGGGATTA[A/G]ATACTTCAGTATTCA | 54455 |
rs538523194 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16247979 | GGTTAAAGCTTCAAG[C/T]AGAAACAAAATGAAT | 54455 |
rs538545993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16301156 | CACCTGCCTTGGCCT[C/T]CCAAAGTGTTGGGAT | 54455 |
rs538644303 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16274240 | GAGCCCAAGAGCTGG[A/G]GCTGCGGTGAGCTAT | 54455 |
rs538653671 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16350265 | GTGCAACATATTATG[A/C]CAAGAAGCATAATGA | 54455 |
rs538659496 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16258259 | TTTCTTGTGATCTCA[C/G]TTAGGGGAACAATAC | 54455 |
rs538663618 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16289847 | GCTAAGGCAGGAGGT[C/T]GAGGCTACAGGGAGC | 54455 |
rs538697138 | snp | G/T | | | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16354177 | ATTTTCAGTAGAAAA[G/T]ACAAAATTCAGTAGA | 54455 |
rs538742732 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FBXO42 | GRCh38.p7 | 1:16295459 | GCAGTGGCATGATCT[C/T]GGCTCACTGCAACAT | 54455 |
rs538783454 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FBXO42 | GRCh38.p7 | 1:16347018 | CCACAGTGCTGGGAT[C/T]ATAGGCATGAGCCAC | 54455 |
rs538805478 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16266459 | ACCACTCTGTGCAGA[C/G]TCGCTTTCTCAGAGT | 54455 |
rs538812451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16271907 | CCTCTGGGAGGCTGA[A/G]GCGGGTGGATCACCT | 54455 |
rs538828888 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16322196 | TTATGGAATTTTGTA[A/C]CTTTTAAGGTATATA | 54455 |
rs538860735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16336815 | ATGGTGAAACCCCGT[C/T]TCTACTAAAAAATAC | 54455 |
rs538893554 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16257642 | TCCTCAAGACCAAAG[C/T]AACTTGTCCCAATAT | 54455 |
rs538895437 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16264945 | CAGTTCCAAATCCTA[C/G]TTTGATTTCTATGCC | 54455 |
rs538923687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16292786 | AAATAAAGACAGTAA[C/T]AGTATTTTGTGACTG | 54455 |
rs538960335 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16329092 | TGCTTGAACCCAGGA[A/G]GCGGAGGTTGCAGTG | 54455 |
rs539000806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16317776 | AAAAAAATAATTAAC[C/T]GGGTGTGCTGGCACA | 54455 |
rs539009987 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16266052 | TTTTTATTTCCTTAA[A/G]AAAATGAAAGTGCTT | 54455 |
rs539043991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16282287 | CTGGAGTGCAGTGGC[A/G]CGATCTCGGCTCACT | 54455 |
rs539078613 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16290262 | AACTGGTATAGATGG[A/T]ATTGTGTCCTCCACC | 54455 |
rs539211759 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16304331 | ACCATGTTGGCCAGG[C/G]TGGTCTCAAACTCCT | 54455 |
rs539231929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16288156 | AACAAACAATAATAA[C/T]AGGCCGGGTGCAGTG | 54455 |
rs539269567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16260606 | ACAGATAAGAAACCT[A/G]AGGGCACAACTCTTT | 54455 |
rs539293930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16273650 | CTTTGGAGGCTGAGG[C/T]GGGCAGATCTCTTGA | 54455 |
rs539310135 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16323571 | GGAGGCTGAGGTGCG[C/T]GGATCTTTTGAGGTC | 54455 |
rs539350958 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16280759 | AGCTTGGGAGAGAGA[A/G]TGAAACCCAGTCTCC | 54455 |
rs539381135 | snp | A/G | 6.76933e-05 | 0.0058174 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16253108 | CACAGCATTGGGACC[A/G]CCACACCCTCCGAGG | 54455 |
rs539388329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16345590 | CGCGGTGGCTCACGC[C/T]TGTAATCCCAGCACT | 54455 |
rs539392276 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16325096 | TACACAAGTTAGCCA[C/G]GCATGGTAGTGCAAA | 54455 |
rs539401984 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16306731 | TTTAGACAGGGTCTC[A/G]CTCTGCTACCCAGGC | 54455 |
rs539414375 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16332532 | CAATGTTTCAACTAA[C/T]GAATTTCTTTTCCTT | 54455 |
rs539451187 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FBXO42 | GRCh38.p7 | 1:16331864 | GAGACCAGCCTGACC[A/G]ACATGGAGAAACCCT | 54455 |
rs539451480 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16339310 | TTTCATATTGTTATA[G/T]TTTTTTTGTTTTTGT | 54455 |
rs539526697 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16275014 | CAACTACTTTAGCCA[A/G]TAAGCAGAAATATCA | 54455 |
rs539533495 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16285330 | CCAGGCTGGAGTGCA[A/G]TGGTGCAATCTCGGC | 54455 |
rs539543589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16333254 | AGATAAATACTAGAG[A/G]TAGTTTCTACTTTTC | 54455 |
rs539568932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16291742 | AGTGGAGCAATCATC[A/G]CTCACTGTAGCCTTG | 54455 |
rs539574791 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16297418 | AAATCCAAATTATCT[C/G]ACCTCTGACACTGTG | 54455 |
rs539582866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16340108 | GTGAACCCGGGATGC[A/G]GAGCTTGCAATGAGC | 54455 |
rs539603041 | snp | A/G | 0 | 0 | intron-variant | FBXO42 | GRCh38.p7 | 1:16312535 | AAAGGATAAACAGGG[A/G]GAGTATACAGGATTT | 54455 |
rs539631452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16276188 | AGATCGAGACCATCC[C/T]GGCTAACACGGTGAA | 54455 |
rs539642620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16344935 | GAAACCCCATCTCTA[C/T]TAAAAATACAAATAT | 54455 |
rs539662548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16303846 | CACCCCCTGGATTCA[C/T]GCCATTCTCCTGCTT | 54455 |
rs539687169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16311596 | ACCAAAGAAGGTATG[C/T]GGGTAACACATAAGC | 54455 |
rs539728038 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16295639 | CTCAGGTGATCCACC[C/T]GCCTCGGCCTCTCAA | 54455 |
rs539815686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16347088 | CTATTGCCATATATA[A/G]TAACTATACATTTAT | 54455 |
rs539827358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16255006 | CATTTGGAGGGCCCA[C/T]CATTTCCACTTGTCC | 54455 |
rs539860952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16254655 | AAATATGAAGATGGA[A/G]ATGCCCTAAGGGAGG | 54455 |
rs539920123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16340958 | ATACCAAAATTTATT[C/T]ATAAAAAATCAGCAG | 54455 |
rs539936060 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16347587 | AGGCAGGGCACTGTG[C/G]CTCACGCCTGTAATC | 54455 |
rs539936694 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B | FBXO42 | GRCh38.p7 | 1:16246722 | TTGGCCAGGCTGGTA[A/T]CAAACTCCTGACCTT | 54455 |
rs539986433 | snp | A/G | 0.00018982 | 0.00974034 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16255815 | GGTTGTCACAATGCA[A/G]TTCCACCTAATGTAA | 54455 |
rs539988428 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | FBXO42 | GRCh38.p7 | 1:16246437 | TGGTCTCAAACTCCT[A/G]GTCTAAGTGATCCTC | 54455 |
rs539988942 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16319965 | TAGTTATGCCTCTTT[C/T]CATGCTCACGTGGGT | 54455 |
rs539992914 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16260750 | ACCCAGGCTGGAGTG[C/G]AGTGGTGTGACTGAT | 54455 |
rs539998348 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16340474 | TAAAGGCGCCCACCC[C/G]GCCCAGCTAATTTTT | 54455 |
rs540042303 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16334897 | ATGGAGTTCTAGAAG[A/G]GTAAACAGTGATCCT | 54455 |
rs540050329 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16268808 | GTCTCTACTAAAAAC[A/G]AACAAACAAACGAAC | 54455 |
rs540060459 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16319641 | TCCTAGGCCAGGTGT[G/T]GTGGCTCACGCCTGT | 54455 |
rs540100316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16254116 | TCTTTCTTCCCCTAC[C/T]TTCCCTAGAAGTCAT | 54455 |
rs540175155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16269276 | ATATTTTTAGTAGAG[A/G]TGAGGTTTTGTCATG | 54455 |
rs540233290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16322279 | GTATCTTTTTCTTCC[A/G]AAAAACTACTATACT | 54455 |
rs540281370 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16341368 | ACACTTTGGGAGGCC[A/G]AGGCGGGCAGATCAT | 54455 |
rs540321351 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16264530 | AGGGTGTCATTCCCA[C/T]TGAGTTCCCATCAAG | 54455 |
rs540328240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16347770 | CGAGGCGGGCAGATC[A/G]CGAGGTCTGGAAATC | 54455 |
rs540329269 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16298222 | TAGAGCAAGACTCTG[C/T]CTCAAAAAACAAAAA | 54455 |
rs540352491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16348658 | GTGAGCAGAGATTGC[A/G]CCACTGCACTCCAGC | 54455 |
rs540358420 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16315889 | AAATAACCGTTTTTC[C/G]ACCAGGCATGGTGGC | 54455 |
rs540369994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16272004 | AAGAAAACAATACAA[A/G]AATAGCTGGGCGTGG | 54455 |
rs540433964 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16326938 | GAACCATTTAATCTT[C/G]CTAATCCCAAAAGGT | 54455 |
rs540493352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16278127 | TTTGGGAGGCCGAGG[C/T]GGGCGGATCACCTGA | 54455 |
rs540515192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16313734 | TTTTGATCTAAAGAT[C/T]GTTCTCTGTTATATC | 54455 |
rs540530383 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16277434 | TTATTTTTAAAAATT[A/C]CATATCCAGGCTGGG | 54455 |
rs540530566 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16269712 | GTATTTTTAGTGGAG[A/G]CGGGGTTTCTCCATG | 54455 |
rs540537153 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16270461 | TCCAGAAAATAATTC[C/T]CAAGGGAAGATTGGG | 54455 |
rs540565836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16321381 | CCCAAGGATATAGAG[A/G]CATTTTGAAACTCTG | 54455 |
rs540575472 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16285805 | CTGGGTGCTCCTTTT[C/T]GAGTCCCCTGATTTC | 54455 |
rs540601192 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | FBXO42 | GRCh38.p7 | 1:16271260 | GCGTGTGTGTGTTGG[G/T]GTGTGTGTGTGTGTG | 54455 |
rs540627960 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16321900 | TAGGCCAGGCGTGGT[C/G]GCTCACGCCTGTAAT | 54455 |
rs540633070 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16269714 | ATTTTTAGTGGAGAC[A/G]GGGTTTCTCCATGTT | 54455 |
rs540650324 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16269321 | CTCAAACTCTTGACC[A/G]TGGGTGATCTGCCTG | 54455 |
rs540683919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16257070 | GTTTTGAGTATTAAA[C/T]AGTATATTCAAAGCA | 54455 |
rs540690268 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16329731 | GAGGCAGGCAGATCA[C/T]GAGGTCAGGAGTTTG | 54455 |
rs540723656 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16323321 | TACTCGGGAGGCTGA[A/G]GCCAGAGAATCGCTT | 54455 |
rs540723949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16330808 | TTAGCTGGGCATGGT[A/G]GTGGGCACCTGTAAT | 54455 |
rs540760659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16330278 | GTAATCCCAGCACTT[C/T]GAGACGCCAAGATGA | 54455 |
rs540790520 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | FBXO42 | GRCh38.p7 | 1:16315014 | GCTGTTCATTAAACT[-/A]AACCAGGGTAAGAAA | 54455 |
rs540851021 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FBXO42 | GRCh38.p7 | 1:16334261 | ACACGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 54455 |
rs540855403 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16292871 | CAATAGGATGCTTAA[C/G]CTGAGAAGATCTTCT | 54455 |
rs540948444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16302540 | TTTGAAACGGAGTCT[C/T]GCTCTGTTGCCCAGG | 54455 |
rs540959427 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16328160 | ATCAAAGAGTGAAAT[G/T]TAATACATGTAAATT | 54455 |
rs540994461 | snp | C/G/T | 0.00517822 | 0.0506191 | intron-variant | FBXO42 | GRCh38.p7 | 1:16303890 | AGCTGCGACTACAGG[C/G/T]GCCCGCCACCATGCC | 54455 |
rs540995836 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | FBXO42 | GRCh38.p7 | 1:16352393 | ACAGCTGGCGGGACC[C/T]CGAGCCGCCCGGAGC | 54455 |
rs541012052 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16345993 | AGGTGACATATCAGA[A/C]GGACACACTACCAAC | 54455 |
rs541020444 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16279138 | CAATTTTTAAGGATA[A/T]CCTGTGGTCTTCCTA | 54455 |
rs541075329 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16348655 | ACAGTGAGCAGAGAT[C/T]GCGCCACTGCACTCC | 54455 |
rs541078674 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16310829 | CAGGAGTTCAAGACC[A/C]GCCTGGCCAACACAG | 54455 |
rs541094157 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16280917 | TTAGGTAAATTACCA[G/T]GTGATTGTGAGCTTT | 54455 |
rs541154894 | snp | C/T | 0.000233209 | 0.0107958 | intron-variant | FBXO42 | GRCh38.p7 | 1:16252440 | AACAAGACTCAGGTG[C/T]GATATGCGTTCCAAA | 54455 |
rs541155135 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16323594 | TTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 54455 |
rs541227636 | snp | A/G | | | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16353107 | GTCCCCCTTCTCAAG[A/G]GAGCAACCTGGTGTG | 54455 |
rs541234828 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16280594 | TTAGGGAAACTGGGT[A/G]TCAGATATATGGAAA | 54455 |
rs541241696 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16248574 | TTAGATAGGAACTAC[C/T]GAGTTTGGAGGCACA | 54455 |
rs541266680 | in-del | -/ATCTT | 0.00993419 | 0.0697739 | intron-variant | FBXO42 | GRCh38.p7 | 1:16338397 | ACAATGTTGCATGAC[-/ATCTT]GTCTTGGATACAGAC | 54455 |
rs541293164 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16348631 | GCTGGAACCCGGGAG[G/T]TAGAGGTTACAGTGA | 54455 |
rs541308810 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16351645 | CCACCCTCCACCGTT[C/G]CCTTTGCACACACAA | 54455 |
rs541321633 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16320066 | CCAAATTCCTATCCT[-/A]AAACGTACAGTCGCC | 54455 |
rs541348681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16310218 | AAAAAAAAATTAGCC[A/G]GGCGTAGTAGCATGC | 54455 |
rs541360069 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16342555 | CCACTGCACTCCAGT[C/T]TGGGAGGCAGATTGA | 54455 |
rs541376768 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16291641 | CTCACCTCAGCCTCT[C/T]GAAGTGCCAGGATTG | 54455 |
rs541385553 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16249227 | ATCTCCTATGCCCAG[A/G]CCATGGTTGAGACTA | 54455 |
rs541393027 | in-del | -/A | 0.0752113 | 0.178743 | intron-variant | FBXO42 | GRCh38.p7 | 1:16348534 | AATCCCACCTCTACT[-/A]AAAAAAAAACTACAA | 54455 |
rs541397749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16296980 | GTCTTGCTGTGTGGC[C/T]GAGGCTGGAGTCCAG | 54455 |
rs541397757 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16303927 | ATTTTTTATATATAT[A/T]TTTTTTTAAGAGACG | 54455 |
rs541403267 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16266130 | GAAAAAGTCAGAACC[A/C]TTTCTACCCCACGGA | 54455 |
rs541403796 | in-del | -/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16276397 | AAAAAAAAAAAAAAA[-/G]AAAAGAAAAGAAAAG | 54455 |
rs541483885 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16303292 | GCATGTTTCAGACTT[G/T]CAGTATTTCCCAACA | 54455 |
rs541510705 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16304871 | CTACTCAGGAGGCTG[A/C]GGCAGGAGAATCATT | 54455 |
rs541511767 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16253544 | TTGGCTTAGTGCATA[C/T]TGGCATCTTACCTGA | 54455 |
rs541561756 | in-del | -/A | 0.152334 | 0.230133 | intron-variant | FBXO42 | GRCh38.p7 | 1:16347993 | CCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 54455 |
rs541566648 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16268614 | AATATAATAACTTAA[A/T]ATATTCCCTTAAATA | 54455 |
rs541585057 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16309756 | TTTTAAAACATTAGC[C/T]GGGTGTGGCCGGGTG | 54455 |
rs541597710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16261502 | ACAAAGTAGGAGCAT[C/T]TTAAATAGCTCAACT | 54455 |
rs541649021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16281670 | TTTTTCTTTCTTTTT[C/T]TTTTTTGAGACGGAG | 54455 |
rs541686825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16289339 | AACCCAGGGGTTTGA[A/G]GCTATAGTCAATTAA | 54455 |
rs541859902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16261883 | CTAATTTTTTTTATT[A/G]TTGTATTTTTAGTAG | 54455 |
rs541912439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16327977 | AAGTGCTGGGATTAC[A/G]TGTGTGACCCACTTT | 54455 |
rs541980078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16299174 | GTGCCACCATGCCTG[A/G]CTAATTTTTTGTATT | 54455 |
rs541992965 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16353030 | AAGAGGATTTAAACT[C/T]AGGCTTGTCTGGTTC | 54455 |
rs541998644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16290308 | AGCCCTAACGCCAAG[A/G]TGATGCTATGGTGGA | 54455 |
rs542064188 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | FBXO42 | GRCh38.p7 | 1:16332546 | ATGAATTTCTTTTCC[G/T]TTTTTTTTTTTTTGA | 54455 |
rs542067693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16305601 | CGCCTGTAGTCCTCA[C/T]ACTCAGGAGGCTGAG | 54455 |
rs542076916 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16273892 | TCTCAAACAAGAAAA[A/G]AAGTGGGATATTCAT | 54455 |
rs542106706 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16267189 | AGATACTAGTTTCTC[C/T]TCTGGTAATAAAAAT | 54455 |
rs542142138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16325255 | AACAACAACAACAAA[A/G]CAGAATTACCTTTAA | 54455 |
rs542173149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16324747 | CTTGAGCCCAGGAGT[C/T]AGATGCTGCAGTGAG | 54455 |
rs542177294 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16332081 | AAGAAAAAGTATATG[A/G]TATCAGTTGCTGGTT | 54455 |
rs542187826 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16348593 | GTACTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 54455 |
rs542200582 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16339858 | TACTTGTGAGTCTGA[A/G]GTAGAGGATCACTTA | 54455 |
rs542234908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16291829 | GGCACATGCCATCAT[A/G]CCCGGCTCATTTTTA | 54455 |
rs542271934 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16256845 | GATCACCTTTCCCTG[G/T]AAGAGCAACAAAAGG | 54455 |
rs542306782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16308006 | GGAGGAGAACAAAGT[C/T]AGAAGATTGATACCA | 54455 |
rs542307322 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16269788 | CCTCGGCCTCCCAAA[A/G]TGCTGGTATTACAGG | 54455 |
rs542336076 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16276148 | GCACTTTGGGAGGCC[A/G]AGGTGGGTGGATCAC | 54455 |
rs542340508 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16248261 | CTTTCCCATGGTACA[C/T]GCCCACAGTGCCCAG | 54455 |
rs542343952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16276504 | TGAATTGGTCCATGG[C/T]ACTACCAAGTGTCCT | 54455 |
rs542354989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16341912 | GGAGGCGGAGGTCGC[A/G]ATGAGCCAAGATCGC | 54455 |
rs542390671 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16274395 | AGGAGCTGACCTCTA[A/T]GGGGGTTGTACAGAC | 54455 |
rs542406080 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16307699 | AACACATATACATTC[A/G]CACCAAAAAATGAAA | 54455 |
rs542421043 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16254161 | TCTGCTCTTTCCACG[A/C]GGCCTCATCTGAGCC | 54455 |
rs542437807 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16262736 | AGGGTCTCACTCCGG[A/T]TGCCCAGGCTAGAGT | 54455 |
rs542459976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16313765 | TCTGGCTGCCTTGTT[C/T]CCCCAGGAAAGAACA | 54455 |
rs542463999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16340341 | TTTTTTTTTTGAGAC[A/G]GAGTTTCACTCTTGT | 54455 |
rs542595869 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16292990 | TCTCAAAAAACAATA[A/C]AAAACAAAACAGAAG | 54455 |
rs542606406 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16301428 | AGCACTTTGGGAGGC[A/T]GAGATGGGCAGATTT | 54455 |
rs542662420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16334958 | ATGGCCACGCGCAGT[A/G]GTTCACACCCGTAAT | 54455 |
rs542702547 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16291369 | TGAGAATCTCATGGG[A/C]CTTTTTTTTTTTTAA | 54455 |
rs542710245 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16258516 | CAAGCACCACCATGC[C/T]CGACTAATTTTTAAA | 54455 |
rs542751861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16265256 | GCACCACCAAGTGGC[C/T]AATTTTGTATTTTTA | 54455 |
rs542765754 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16259221 | AATTAGAAAGCCTAA[A/G]TAATATAATGGTCTA | 54455 |
rs542768050 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16293737 | AGGTTTAAGTCCCTG[C/G]CCTAGACATTCACAG | 54455 |
rs542769809 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FBXO42 | GRCh38.p7 | 1:16346047 | ATTTCAGGGTCAGAA[C/T]GACTAATGGTGAGAA | 54455 |
rs542772815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16314656 | TTGGGACGCTGAGGC[A/G]GGCGGATCACGAGGT | 54455 |
rs542819955 | in-del | -/AAAAG | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16274323 | AAAAAACACAAAAAA[-/AAAAG]AAAAGAAAAGAAAAA | 54455 |
rs542855716 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16324873 | TTTCAGAGAATAAAA[C/T]TGGGGAAGGTGAAGG | 54455 |
rs542862960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16255874 | ACCACACACTTTATG[C/T]AAAAATAGTAAGTAG | 54455 |
rs542869259 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16335664 | AGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 54455 |
rs542870370 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16266319 | AGGAAAAGAGCCATG[C/G]TAAAATAAGTTTGCT | 54455 |
rs542953154 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16278925 | CTGGGACTACAGGCA[G/T]GTGCCACCATGCCTG | 54455 |
rs542981366 | in-del | -/TCT | 0.00318978 | 0.0398085 | intron-variant | FBXO42 | GRCh38.p7 | 1:16311479 | GGTGACAGAGCAAGA[-/TCT]TGTCTCAAAAAAAAA | 54455 |
rs542987629 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16325906 | GCTGGGATTACAGGC[A/G]TGAGCCACCACACCT | 54455 |
rs543030746 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16338244 | CCAGCCTGGACAACA[G/T]AGCGAGACTCCATCT | 54455 |
rs543049396 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16281094 | CAGCCTCCCGAGTAG[C/G]TGGGATTACAGGCAT | 54455 |
rs543050561 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16288412 | TCCAGCCTGGTGACA[C/G]AGCGAGACTCCATCT | 54455 |
rs543050955 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16297775 | AGGAGGCTGAGGCAA[C/G]AGACTGGCATGAACC | 54455 |
rs543054719 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16309978 | AGGCAGGCAGATCAC[A/G]AGGTCAGGAGATCGA | 54455 |
rs543107512 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16324445 | CAAAACAAGAAGCCT[G/T]AACAGTTCAAGAAAG | 54455 |
rs543107627 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16317391 | CCGCACTCCAGCCTG[A/G]GCAATAGAGTGAGAT | 54455 |
rs543129105 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16350606 | AAAAAAAATTAGCGG[G/T]CGTGGTGGCGCACAC | 54455 |
rs543144524 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16309991 | ACAAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT | 54455 |
rs543149049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16257963 | TGGGATTACAGGCGT[A/G]AGCCACCATGCCTCG | 54455 |
rs543163821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16273915 | ATATTCATATTAAGA[A/G]GCACTCATGGTAATG | 54455 |
rs543192144 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16349699 | AACCTTGTCTCTACT[A/G]AAAATACAAAAAATT | 54455 |
rs543261303 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16328886 | ATTGATGGGATTGGC[C/G]GGGTGCGGTGGCTCA | 54455 |
rs543270312 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250384 | GCAAGGTAGAAAAAG[A/G]CAGCCCAGCCCCTGT | 54455 |
rs543290556 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16302658 | GGGACTATAGGCACC[C/T]GCCACCAGGCCCGGC | 54455 |
rs543336065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16287502 | GGCATATAGAACAAT[A/G]CCAGGGGGGCAATCC | 54455 |
rs543387379 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16345761 | GCTGAGGCAGGAGAA[A/T]GGCATGAACCGGGGA | 54455 |
rs543400346 | snp | A/G | | | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16353602 | CCAGGCTGGAGTCCA[A/G]TGATGAGTTCTTGGT | 54455 |
rs543410704 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16343247 | AAAAAATTCTAAGGA[C/T]TTAGAAGAACTGCAG | 54455 |
rs543469834 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16274410 | TGGGGGTTGTACAGA[C/G]AGGAAAGGGGCATGA | 54455 |
rs543471756 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16335587 | AACTTTTGACTGGGC[C/G]AGGCACAGTGGCTCA | 54455 |
rs543548524 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16338896 | GCTCACTGCAACCTC[C/T]GCCTCCCAAATTCAA | 54455 |
rs543619077 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16343606 | AGGCAGGTACATCAC[A/G]AGGTCAGGAGTTCAA | 54455 |
rs543622508 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16247297 | CCCCACTGACTTGTG[C/T]GCTGGTAAGAGACCA | 54455 |
rs543670888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16345139 | ATATATATATATTTT[C/T]TGAGCCAGGCGCGGC | 54455 |
rs543712963 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16252608 | TATTACCACTGGCTT[A/C]GCACATGGAATTGTG | 54455 |
rs543736006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16303977 | AAGATGGAATTGTTC[A/G]TATTTTTAGCAGAGA | 54455 |
rs543739959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16336453 | AACCTCCACCTCCTG[A/G]GTTAAAGCAGCTCTT | 54455 |
rs543789622 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16261939 | GGATGGTCTCGATCT[C/T]CTGACCTTGTGATCC | 54455 |
rs543791372 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16298133 | GGGGAGGCTGAGGCA[A/G]TAGAATCGCTCGAAC | 54455 |
rs543799041 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16289598 | TCCTCTAACATGTCC[A/T]TTTCTTTGCTGCACC | 54455 |
rs543825423 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16353696 | GACTACAGGCGGGCA[C/T]CACCATGCCTGGCTA | 54455 |
rs543827840 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16305648 | AGCCTGGGGAGGTGG[A/T]GGCTGTAGTAAGCTG | 54455 |
rs543833570 | in-del | -/TT/TTT | 0.375 | 0.216506 | downstream-variant-500B | FBXO42 | GRCh38.p7 | 1:16246509 | ACTGTGATTGACCTC[-/TT/TTT]TTTTTTTTTTTTTTG | 54455 |
rs543877789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16297675 | GACCATCCTGGCTAA[C/T]ACAGTGGAAACCCCA | 54455 |
rs543950009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16262568 | AAAAATTAGCCAGGT[A/G]TGGTGGCATGTGCCT | 54455 |
rs543951827 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16299263 | TGATCCGCCCGCCTC[A/G]GCCTCCCAAAGTGCT | 54455 |
rs543999557 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16310317 | AATGAGCTGAGACTG[C/T]GCCACTGAACTCCAG | 54455 |
rs544009113 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16331394 | CACTCCAGCCTGGGC[A/G]ACAGAGCGAGACTCT | 54455 |
rs544035773 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16319553 | CAGTGAGAAAGGAGC[-/A]AATTCCCTTCATTCC | 54455 |
rs544074164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16268704 | CACAGCAGCTCACGC[C/T]TGTAATCCCAGCACT | 54455 |
rs544074943 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16287593 | CTGTAGAGTCATTTA[C/T]TTTTTATTATTTTTG | 54455 |
rs544080519 | snp | G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16352783 | ACTTCTACCCCGAGG[G/T]CCCGATGAGCAGAGA | 54455 |
rs544091113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16325347 | TAATATTTTAAATTC[C/T]ACATTAACGAAGCAT | 54455 |
rs544113605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16282530 | TGTGCCCGGCCATTT[C/T]CTCTTTTAAAAAAAA | 54455 |
rs544169791 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16260277 | GTAATGGCACGATCT[C/T]GGCTCACTGCAACCT | 54455 |
rs544203824 | in-del | -/CTAGA | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16259404 | AGTAATGTAAACTCT[-/CTAGA]CTAGAATGTGGATTT | 54455 |
rs544216199 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16333639 | TTTTACTTCTCATTG[C/T]TATGGCTTCCAATAA | 54455 |
rs544232893 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16312633 | ATAGAATGCACAACA[C/G]CAAGCATGAACATTA | 54455 |
rs544233528 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16285022 | GTGGTGGCACGTGCC[C/T]GTAATCCCAGCTACT | 54455 |
rs544253444 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | FBXO42 | GRCh38.p7 | 1:16254838 | CAGAAGTGGACAGGA[C/G]AGGAGGTAGGGACAA | 54455 |
rs544275671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16306299 | TGAGATTACAGGCAT[A/G]AGCCACCGCGCCCAG | 54455 |
rs544279092 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16338925 | AAGCAATTCTCCTGC[C/T]TCAGCCTCCTGAGTA | 54455 |
rs544312842 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16347022 | AGTGCTGGGATTATA[C/G]GCATGAGCCACCGCA | 54455 |
rs544354733 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16271148 | TAAAATACAGTGAGG[G/T]ACAGGAATGCAGCAG | 54455 |
rs544369655 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16321833 | AAAGTGCTGGGAATA[C/G]AGGTATAAGTCACTG | 54455 |
rs544372289 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16330092 | AAGTTATTATATTAT[C/T]ATCACACAATGTAGC | 54455 |
rs544518695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16292774 | AGCTTGTTTACAAAA[C/T]AAAGACAGTAATAGT | 54455 |
rs544524747 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16284455 | GATATTGCTCTAACA[A/G]TTCTCCCCCTCTATC | 54455 |
rs544576258 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16327172 | ATCATAAAGTACCTT[A/C]CTGACGAGGGATGTT | 54455 |
rs544592846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16277343 | ATTAAAAAGCAGAAT[C/T]GAATAGTGACAAGCA | 54455 |
rs544626801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16335005 | GCCAAGGTGGGCGAA[C/T]AGCTTGAGCCCAAGA | 54455 |
rs544633289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16294472 | GACTCTGTGTTTCTG[C/T]TCTTACTTCAACCTC | 54455 |
rs544677388 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16270009 | CACAGACATGCAAAC[C/G]ACAGCTGGCTAATTT | 54455 |
rs544691823 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16263358 | GAGGCTGAGGCAGGA[C/G]AATGGCGTGAACCCG | 54455 |
rs544699125 | snp | A/T | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16249107 | GAAATTAGGATTTAA[A/T]TTTCAAAACAAAACA | 54455 |
rs544703571 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16270374 | TCTCTGCTAGATGGA[C/G]TTAGGCAGCAGTAAA | 54455 |
rs544740880 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16272794 | CTTTTCCTGATGTTA[C/T]AACTTCTAGCCTTTA | 54455 |
rs544741159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16335734 | TAGCTGGGCGTGGTC[A/G]TGGGCACCTGTAATC | 54455 |
rs544879884 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16307318 | AGCCCGGGCAACATA[C/G]CAAGACCCCATTTCT | 54455 |
rs544970539 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | FBXO42 | GRCh38.p7 | 1:16347211 | ACACTGGAAAAAATT[A/T]AAAACTCAGAAAAAA | 54455 |
rs545004416 | in-del | -/C | 0.00993419 | 0.0697739 | intron-variant | FBXO42 | GRCh38.p7 | 1:16290681 | TGGGTGACAGAGTGA[-/C]AAAAAAAAAAAAAGA | 54455 |
rs545057125 | snp | A/T | 3.29544e-05 | 0.00405908 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251330 | ATTCAGATCTATGGA[A/T]CCTAATCTCAGATCT | 54455 |
rs545085948 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16317052 | TTGGGAGGCTGAGGC[A/G]GGCGGATCACCTGAG | 54455 |
rs545142284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16259178 | GTCAAAAACATTTAC[C/T]TCCCCAAGGGGATCT | 54455 |
rs545151851 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16303256 | GCTGAAGCTTGCTGA[C/T]GGAAGAATGCAAGGC | 54455 |
rs545206042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16256025 | AGTTCTGAATGTAAA[C/T]GGTCTGGAGGGAGAG | 54455 |
rs545258679 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16294355 | TAACTAGCAGAGGCA[C/T]GTCCCATACACTCCC | 54455 |
rs545275012 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16258912 | CCAGCTAATTTTTAA[A/G]ATTTTTTTGTTGTGA | 54455 |
rs545346298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16265338 | TCAGGTGGTCCTCCC[A/G]TCTTGGCCCCCCAAA | 54455 |
rs545352910 | snp | A/G | 0 | 0 | intron-variant | FBXO42 | GRCh38.p7 | 1:16350689 | GGGATGGAGATTGCA[A/G]AGAGCCGAGACTGTG | 54455 |
rs545364997 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16351337 | AGTTGTTCTCAAAAA[A/G]GAACAACATAGTTTC | 54455 |
rs545366307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16257007 | CTCTCTCATGTTTAT[A/G]ATTTGCTCACCTAAA | 54455 |
rs545385417 | snp | C/T | 0 | 0 | intron-variant | FBXO42 | GRCh38.p7 | 1:16272858 | GGAATATTTCATTTT[C/T]ATGAAAGTATCAACC | 54455 |
rs545402028 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16263177 | GCCATTTAAAGAGTG[C/T]CTAAGCCAGGCGCGG | 54455 |
rs545426208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16281574 | CCCAGGTTCAAGCAA[C/T]TCTTGTGCCTCGGAC | 54455 |
rs545451717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16318049 | AGTTCTGTTTCCTGA[C/T]TGGGTACTGGTTACA | 54455 |
rs545465334 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16295999 | GCCTTCTTTGATTAG[A/G]TGATTGTATACACAT | 54455 |
rs545478301 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16274521 | AAAATCTCTGAGTTG[G/T]GCACTTAAGATTTGC | 54455 |
rs545493829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16324712 | GTCCCAGCTACAGGG[A/G]GTCTGAGGTGCGAGC | 54455 |
rs545577399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16272346 | CTCACCGCAACTCCC[A/G]CCTCCCGGGTTCAAG | 54455 |
rs545615304 | in-del | -/A | 0.114036 | 0.209795 | intron-variant | FBXO42 | GRCh38.p7 | 1:16340177 | CAAGACTCCAGTCTC[-/A]AAAAAAAAAAAGTAA | 54455 |
rs545620271 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16265713 | AGAAATCCAACCTAA[A/G]GGGTTATTTAATGAA | 54455 |
rs545650610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16279080 | CGCGCCCAGCCTAGA[C/T]GGTTATTTCTGAACA | 54455 |
rs545654105 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16307307 | AGTTTGAGACCAGCC[C/T]GGGCAACATAGCAAG | 54455 |
rs545711220 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16281193 | TCTCGAACTCCTGAC[C/G]TCAGGTGATCCGCCC | 54455 |
rs545813181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16332320 | TCCAACAATGGGAGG[C/T]ACATTGTTATTATTA | 54455 |
rs545863209 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16352521 | GGCGGACGCGCGCGC[A/T]CTCACGTCAGCGCGG | 54455 |
rs545926252 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16332796 | TATGCCTGCCTCGGC[A/C]TCCCAAAGTGCTGGG | 54455 |
rs545932469 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16266651 | GGAGCCTCAAACTGG[C/T]GTGTGTATGGGGGGT | 54455 |
rs546031276 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16304052 | TCAGGTGATCCGCCC[A/G]CCTTGGCCTCCCAAA | 54455 |
rs546044208 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16337130 | AATCATTAGGTACTC[A/G]GAGGAAATCTCATTC | 54455 |
rs546045558 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16338998 | GTATTTTTAGTAGAG[A/C]TGGGGTTTCACCATG | 54455 |
rs546119498 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16331348 | AACCCGGGGGAGGCA[C/G]AGCTTGCAGTGAGCC | 54455 |
rs546225586 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16345904 | CGACTAATTTCACTT[C/T]AATGACAGGTAGATA | 54455 |
rs546306373 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FBXO42 | GRCh38.p7 | 1:16283850 | AATGGGTTTGGGTTA[A/G]TCTCTAAGCAGTTTT | 54455 |
rs546319638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16290986 | AAAAAGACATCTGAT[A/G]CAGCAGTATTCTCTA | 54455 |
rs546347231 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16353236 | AAACAAAACAAAACA[A/C]AACAAAAAACTAAGC | 54455 |
rs546405293 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16261309 | GTAAGCTGAGGCCAG[A/T]GATAATGATAAATCA | 54455 |
rs546454462 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16292357 | ACACAGTCTCACTCT[C/T]GCCTAGGCGTCTGGG | 54455 |
rs546462056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16254279 | TAATTGGTGACAGCA[A/G]GAAATAGACACTGGT | 54455 |
rs546467447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16346381 | AATGAACTACTTCAA[A/G]TCTATTTATTACTAG | 54455 |
rs546528848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16291454 | GGCGCAATCTTGGCT[C/T]ACTGCAACCTCTGCC | 54455 |
rs546529339 | snp | A/T | 1.75665e-05 | 0.0029636 | intron-variant | FBXO42 | GRCh38.p7 | 1:16253771 | AAGGTAGTTAGGAGC[A/T]CCCAGGGACCATAAT | 54455 |
rs546546482 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16339324 | AGTTTTTTTGTTTTT[C/G]TTTTTTTGAGATGAA | 54455 |
rs546570439 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16253537 | ATTTTCTTTGGCTTA[A/G]TGCATATTGGCATCT | 54455 |
rs546629958 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16349776 | CTGAGGCAGGAGAAT[C/T]GCCTGAACCGGAGAG | 54455 |
rs546636366 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16347593 | GGCACTGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 54455 |
rs546674928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16333528 | GAGGCTGAGGTGGGA[A/G]GATCACCTGATGATT | 54455 |
rs546676827 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16326298 | CGACCTCAGGTGATC[C/T]ATCTGCCTGGGCCTC | 54455 |
rs546700459 | in-del | -/TTTA | 0.00199481 | 0.0315187 | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16353961 | CGAACCAATGTAGTT[-/TTTA]TTTATTTATTTACTT | 54455 |
rs546750781 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16261711 | GTATATCAATTTTTT[G/T]TTTTTGTTTTTGAGA | 54455 |
rs546754185 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16267737 | ATTAGACAAAACTTG[C/T]CTGGATCTCAGGATT | 54455 |
rs546762333 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16333026 | CTCTGCTCTTGCTGG[A/C]CATCCCCTCTTGCAG | 54455 |
rs546790771 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16305115 | AATGGCCAGGCACAG[G/T]GGCTCACACTTGTAA | 54455 |
rs546804964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16324233 | TATATGTAAAAATAC[C/T]GTGCTTATTGCAAGC | 54455 |
rs546819194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16284558 | AAAAACGAGCTGGGC[A/G]TGGCAGCTCATGCCC | 54455 |
rs546820924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16276235 | AATACAAAAAATTAG[C/T]CGGGCATGGTGGCAT | 54455 |
rs546871806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16269320 | TCTCAAACTCTTGAC[C/T]GTGGGTGATCTGCCT | 54455 |
rs546891195 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16322071 | GCTACCTGGGACATG[A/T]AAAAAAAATTACATC | 54455 |
rs546899365 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16305685 | TGCCACTGCACTCCA[C/G]CTTGGGTGATAGAGT | 54455 |
rs546900071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16319983 | TGCTCACGTGGGTAA[A/G]GTGTTTTTCAACATG | 54455 |
rs546991915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16255541 | GGCTTCGCCATGTTC[A/G]CCATGCTGGTCACAA | 54455 |
rs547068829 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16247789 | AAATGAAGGGTGGAA[A/G]TAGGAATGAAAACAC | 54455 |
rs547115603 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | FBXO42 | GRCh38.p7 | 1:16348323 | CAACAACTACAGCAC[A/T]AAGGTAAATAACTTG | 54455 |
rs547145426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16264784 | AGACACCCTATACAA[C/T]AGAACTAACATTCCC | 54455 |
rs547156663 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | FBXO42 | GRCh38.p7 | 1:16246754 | TGATCCGCCTGCCTC[A/G]GCCTCCCAAAGTGCT | 54455 |
rs547169653 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16334447 | AAAAAAAAACAGACT[G/T]ATTCTACAGATAAGA | 54455 |
rs547209653 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16322926 | GGGAATGAAACTGCT[A/G]TGCATTTAAAAGCCA | 54455 |
rs547235856 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | FBXO42 | GRCh38.p7 | 1:16293975 | GTAATCAAAGTAGTA[A/C]GGCAAGGCCTAAATA | 54455 |
rs547328120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16328526 | AAGATAGAATGATCC[C/T]GTGATAATGGATTAG | 54455 |
rs547329988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16335342 | AGGATTTCGCCACAT[C/T]GCCCAGGCTGGTCTC | 54455 |
rs547385563 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16322080 | GACATGTAAAAAAAA[G/T]TACATCATTAGTATA | 54455 |
rs547390718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16286102 | GTCTCAAACCCTTAG[A/G]CTGAAGCAATTCTGC | 54455 |
rs547404794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16271826 | ACCTGCATACCTAGC[A/G]TAGTCATTGGATGCT | 54455 |
rs547458253 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16343586 | CCCAGCACTTTGGGA[A/G]GCCGAGGCAGGTACA | 54455 |
rs547461160 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16316119 | AGTTGCAGTGAGCCG[A/C]GATCATGCCACTGCA | 54455 |
rs547469099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16264086 | AAAGTGCAGGGATTA[C/T]AGGCATGAGCCACCA | 54455 |
rs547485578 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16280054 | GGTTTCTCTATGTTG[A/G]CCAGGCTGGTCTTGA | 54455 |
rs547494309 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16283459 | TGAGCTTTAAATCTT[C/T]ACCTGGCATTTATAG | 54455 |
rs547497582 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16315639 | CCAAAGGCTTTTGAT[G/T]ACATTTTTTCTCTTC | 54455 |
rs547504391 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16308467 | CCATTGAATTTCAGC[C/G]TGGGAAACACAGTGA | 54455 |
rs547520609 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16272413 | TACAGGCATGCACCA[A/C]CACGCCCAGCTAATT | 54455 |
rs547522414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16285473 | GAGACGGGGTTTCAC[C/T]ATGTTGGTCAGGTTG | 54455 |
rs547665924 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16285869 | ACCATTCTCTTTTTT[A/G]TTTTTGTTGTTCTTT | 54455 |
rs547729919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16350855 | AAGCTTTTTAAGATA[C/T]GCAACATGCCTATGG | 54455 |
rs547741207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16343882 | TACTCGGGAGGCTGA[A/G]GCAGGAGGATCGCTT | 54455 |
rs547782473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16303664 | CCTCCGCCTCCCGGG[C/T]TCAAGTGATTCTCCT | 54455 |
rs547856807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16297805 | CCGGGAGGCGGAGCT[C/T]GCAGTGAGCCAAGAT | 54455 |
rs547864740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16331052 | CTTGAACCAGGAGGC[A/G]GAGGTTGCAGTGAGC | 54455 |
rs547866652 | snp | C/T | 0 | 0 | intron-variant | FBXO42 | GRCh38.p7 | 1:16323522 | AGGGACAGGGCCGGG[C/T]GCAGTGGCTCACGCC | 54455 |
rs547942304 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16338583 | TAGAGATTATTCTGC[A/T]GTCTCCAGGAATTTA | 54455 |
rs547954126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16330573 | CAGCACTTTGGGAGG[C/T]TGAGGCAGGCAGATC | 54455 |
rs547969494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16274066 | ACACAGAACTATACT[C/T]TGGGAATCTGAGGCA | 54455 |
rs547983692 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16302383 | TTTATAAAGGAAAGA[C/G]GTTTAACTGACTCAC | 54455 |
rs548037562 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16336095 | GGCGCCTGCCACCAT[G/T]CCCGGCTAATTTTTC | 54455 |
rs548043951 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16267192 | TACTAGTTTCTCTTC[A/T]GGTAATAAAAATATT | 54455 |
rs548057499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16295230 | GGGAAATTTCAGCAC[A/G]GCTACATAATTGATC | 54455 |
rs548063532 | in-del | -/AG | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16270706 | AAAAAAGAAAAGAAA[-/AG]AAAGAAGAAAAGATA | 54455 |
rs548072944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16343096 | CTTTACAGAAACACA[A/G]AATGGACTAAGACAC | 54455 |
rs548150264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16260493 | GGATTACAGGTGTGA[A/G]CCACCGCGCCTGGCC | 54455 |
rs548168946 | snp | C/T | 0.00398564 | 0.0444627 | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16352566 | GCGGCCAGGGGGCGG[C/T]GCAGTGTTGAGAAAG | 54455 |
rs548169779 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16311350 | AAAATTAGCTGGGTG[C/T]GGTGGTACACACTTG | 54455 |
rs548178617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16310484 | TGCAGTGAGCCCTGA[C/T]CACGCCACTAGACTC | 54455 |
rs548214274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16317633 | CAAACAAACAGAAGA[C/T]AGAAGAATGGGCAGG | 54455 |
rs548214466 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16299659 | TTATTATTATTATTT[C/T]TTTGAGATGGAGTCT | 54455 |
rs548231764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16352072 | TGGAAAGGAGCTGTC[C/T]TCCTCCTCGCCTCAC | 54455 |
rs548236328 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16292407 | GCAATCCTCCTGTCT[A/C]ACCCTCCCAAGTATC | 54455 |
rs548274148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16345986 | AGACCAAAGGTGACA[C/T]ATCAGAAGGACACAC | 54455 |
rs548305673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16319708 | ACGAGCTCGGGAGTT[C/T]GAGACCAGCCTGGCC | 54455 |
rs548308310 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16345391 | TCCTGCCACTGAACT[A/C]CAGCCTGGGTGATGG | 54455 |
rs548308610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16252827 | ATATGATAGCAGTAA[A/G]CTTTATAGCCTAAAA | 54455 |
rs548313617 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16353264 | AGCCCCCACCCCCCC[A/C]CCAACACCAAACCAT | 54455 |
rs548385449 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16323214 | ACAAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 54455 |
rs548420761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16312323 | GCCAAAATCGCACCA[A/G]TGCACTCCAGCCTGG | 54455 |
rs548456064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16282121 | TTACTGTAATAACAC[C/T]GAGAGAGCTCACATA | 54455 |
rs548458949 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16351563 | TCAAACGAACTCAGC[A/G]CTGAAGTTACTCTGC | 54455 |
rs548520872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16270137 | CTGGGATTACAGGTG[C/T]GAGCCACCACGCCCA | 54455 |
rs548549643 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16289906 | GATGACAGAGTAAGA[C/T]CTTGTCTCAAAAAAA | 54455 |
rs548631363 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16262225 | ATGGGGTCTTGCTAT[C/G]CTGCCCAGTCTGGTC | 54455 |
rs548651893 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16312946 | ACTACAGGCACCCAC[C/G]ACCATGCCTCACTAA | 54455 |
rs548728695 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | FBXO42 | GRCh38.p7 | 1:16346692 | GACTCCGTCTCGGGG[A/G]AAAAAAAAAAAAAAC | 54455 |
rs548743723 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16339157 | CAAAGGAATGCCTTC[C/T]TGCTTCTGCCTCCTA | 54455 |
rs548790286 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16354131 | TAGCTGGGATTACAG[A/G]CGCCCGCCACCGTGC | 54455 |
rs548828988 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16285311 | TCTTCCCATGCTCTG[C/T]TGCCCAGGCTGGAGT | 54455 |
rs548906133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16332341 | GTTATTATTACCATT[A/G]CTATAGTTGAATGAA | 54455 |
rs548924440 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | FBXO42 | GRCh38.p7 | 1:16284656 | CCAAGATAGTGAAAC[A/C]CCATCTCTACTAAAA | 54455 |
rs548966999 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16301128 | GGTCTCCAACTCCTG[G/T]CCTGAAGTGATCCAC | 54455 |
rs548975868 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16347038 | GCATGAGCCACCGCA[C/T]CCGGCCTGTCAGAAT | 54455 |
rs549044204 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16294081 | AATGTTTTGGGAAAA[G/T]CTTGCCAAAAAATCT | 54455 |
rs549083175 | in-del | -/TGA | 0.00398564 | 0.0444627 | intron-variant | FBXO42 | GRCh38.p7 | 1:16260941 | ACTCCTGGCCTCAAG[-/TGA]TTCTCCCACCTCTGC | 54455 |
rs549085909 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16257110 | ATGCCTGGCACATAG[A/G]AAGTGCTCAACAAAT | 54455 |
rs549139688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16254340 | AAAGAAGAGAAAAAA[C/T]GATTCAAAAGGCAGC | 54455 |
rs549163130 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16270589 | CACGCCTGTAATCCC[A/T]GCACTTTGTGAGGCT | 54455 |
rs549173209 | snp | A/G | | | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16353508 | AACTTTGGTGTCCAC[A/G]ATCCCTTATCATAAC | 54455 |
rs549245273 | in-del | -/GCCTGTAATCCCAACACTTTGGGA | 0.0209421 | 0.100162 | intron-variant | FBXO42 | GRCh38.p7 | 1:16296389 | GGTGCAGTGGCTCAT[-/GCCTGTAATCCCAACACTTTGGGA]GCCTGTAATCCCAAC | 54455 |
rs549274706 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16300122 | CCAGTAGTAATTTCC[C/T]TTTTCACAAGTTCTC | 54455 |
rs549294773 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | FBXO42 | GRCh38.p7 | 1:16252113 | TGAGTAGGGCCCCTG[-/T]TAAGTTTTCCCATTT | 54455 |
rs549297294 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | FBXO42 | GRCh38.p7 | 1:16278389 | AACAAAACAAAAAAA[A/C]CCACATCCAGCTGTT | 54455 |
rs549334291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16258100 | TAACCTGACAGCAGT[C/T]GAGATGCTCCAATCT | 54455 |
rs549337959 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16247954 | AAGGCACACTTGCAG[A/G]AATGGAAGGGGTTAA | 54455 |
rs549349077 | in-del | -/T | 0.297636 | 0.24542 | intron-variant | FBXO42 | GRCh38.p7 | 1:16274758 | ACCATGCCCAGCTAA[-/T]TTTTTTGTATTTCAG | 54455 |
rs549462128 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16342768 | TAGGAGGTGGGGCCT[A/C]CTGGGTGGTGTTTAG | 54455 |
rs549495601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16316836 | AGAAAATATGAATCA[C/T]TAAGAGATCCAGGCA | 54455 |
rs549498829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16342062 | TGGGTGGATCACCTG[A/G]GCCCAGGGGTTCAGG | 54455 |
rs549581943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16258821 | GGCTCACTGCAGCCT[C/T]GACTTCCTCAGGCTG | 54455 |
rs549603996 | snp | C/T | 1.64887e-05 | 0.00287125 | missense, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16294797 | CCTGAAGCCAAAGGT[C/T]GGATCCACTCTTTGC | 54455 |
rs549604422 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16309810 | AGCATTTTGGGAGGC[C/T]GAGGTGGGTGATCAC | 54455 |
rs549640408 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16307624 | GATTGCAGGATACAA[C/G]GTTAGCATACAACAA | 54455 |
rs549670005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16286858 | CTTGATTGCTTTCTT[C/T]CTCTTTCCTACTCTA | 54455 |
rs549681190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16314892 | CCGTCTGAAAAAAAA[A/G]AAAAGAAAAGAACAA | 54455 |
rs549686140 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16335856 | TGGGTGACAGTGCGA[C/G]ACTCCATCGCGCCAA | 54455 |
rs549725137 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16247975 | AAGGGGTTAAAGCTT[C/G]AAGTAGAAACAAAAT | 54455 |
rs549782108 | in-del | -/T | 0.0788843 | 0.182262 | intron-variant | FBXO42 | GRCh38.p7 | 1:16258004 | TTTTTTTTTAAAATC[-/T]TTTTTTTTTTCTTTT | 54455 |
rs549800114 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16273139 | TGAAAGGTAGGTATT[A/T]CCATCTCTACCCTAA | 54455 |
rs549829683 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16279168 | ACTGACATGTGATAT[G/T]ACCAATACTTTTTCC | 54455 |
rs549856767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16258138 | GAGCTTTGCTTCCTC[C/T]TTCAGTAGCACATTA | 54455 |
rs549877328 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | FBXO42 | GRCh38.p7 | 1:16275285 | TACAGAAAAGAGGAA[A/G]TTATCAGGGGCACAA | 54455 |
rs549899496 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16339704 | ATGAATTTATGAAAG[A/G]TAGATAATGTCTTGA | 54455 |
rs549912660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16265550 | ATTATAACCTTAAAA[C/T]GCAGGTATTACTAGC | 54455 |
rs549926309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16329177 | CAAAAAAAAAAAAAA[A/G]AAAAAGAAAATTGAT | 54455 |
rs549949802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16343920 | GAGATTGGGGCTGCA[C/T]TGAGCCATAATCACA | 54455 |
rs549958677 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16333955 | AAAATTGATTTTGCA[A/T]ACTGTATCAACTGTA | 54455 |
rs550022993 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16337594 | TCCTCAAAAGAATAA[C/T]AGGCCAGGCCAGGCA | 54455 |
rs550062660 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16254485 | AAGGGACCAACATGA[C/T]GAGGACAGACTCCTG | 54455 |
rs550089602 | snp | A/G | 0.000115316 | 0.00759243 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250883 | TTTAATGTCCAGCAC[A/G]TACATCTGCATGGGC | 54455 |
rs550110831 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16344595 | CCCACCTCAGCCTCC[A/C]AAAGTGCTGGGATTA | 54455 |
rs550164453 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16348626 | GAATCGCTGGAACCC[A/G]GGAGGTAGAGGTTAC | 54455 |
rs550217807 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16337075 | GTTTCAGCTAAGAGT[A/G]CACAGCAAAAACAAC | 54455 |
rs550243865 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16290881 | AAGCTACCCAGTCTA[C/T]GGTATTTTGTATGGC | 54455 |
rs550246577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16288814 | TATACAAAAATTAGC[C/T]TGGTGTGGTGGCACA | 54455 |
rs550312728 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16351781 | TAGGAAAGGCCTTTT[C/G]TGTTTTATTTAACGT | 54455 |
rs550338235 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16324047 | CTGTTGAATGAGAGA[C/T]TTAAAGAAGATCATA | 54455 |
rs550360220 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16267317 | GAAATAGGAAGTAAA[C/T]ACAAAGTTACAGAAC | 54455 |
rs550363016 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16296274 | AAAATAAAATAAAAT[G/T]AAGTAAACAAAAAAG | 54455 |
rs550363530 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16332384 | ATATCTATTATTCTC[A/C]AAAAAAAATGCTTAT | 54455 |
rs550364870 | in-del | -/A | 0.0111196 | 0.0737302 | intron-variant | FBXO42 | GRCh38.p7 | 1:16302513 | GGGGAAACTGCCACC[-/A]TTTTTTTCTTTTTTG | 54455 |
rs550397256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16266392 | TCAGGAGACTGAGGC[A/G]GGAGGATGGCTTAAC | 54455 |
rs550403546 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | FBXO42 | GRCh38.p7 | 1:16314306 | TTGCTGTTTAGAGAT[-/A]AAATCAAGTGACAAA | 54455 |
rs550432564 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16350308 | ATGTTTTACTGCATT[A/G]ATTTCATGACTCTTT | 54455 |
rs550440699 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16252833 | TAGCAGTAAACTTTA[C/T]AGCCTAAAAAGGAAA | 54455 |
rs550468952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16260539 | TTTTTAAGTGCTTTG[C/T]ATGTATTAATTAATT | 54455 |
rs550480208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16287999 | AAAATACAAAAAATT[A/G]GCTGGGTGTGGTGGT | 54455 |
rs550486057 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16264166 | AAGTAATGACTTTGA[A/G]GAACTGCCCGAATGT | 54455 |
rs550517552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16298518 | CCTATGAGTTATTTA[C/T]TTATTTTCTGAGATG | 54455 |
rs550544067 | in-del | -/G | | | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16353352 | GGTTCAGGCCATGAC[-/G]GGAAGCAGGACATGA | 54455 |
rs550556518 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16305003 | AAAATTCTTAACAAA[A/C]TGCCTACAATATATT | 54455 |
rs550571089 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16313117 | TTTGTTTCTCCTACT[C/T]AATTTTGCTGTGAAC | 54455 |
rs550571168 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16320406 | CTTTTATTACTGGAA[A/G]AAATATCACTTCCCA | 54455 |
rs550594179 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16304311 | TTTTTAGTGGACAGG[G/T]TTTCACCATGTTGGC | 54455 |
rs550599112 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16324313 | TTAGATCCCACACAG[A/G]GTACAAAAAGAAGAT | 54455 |
rs550690675 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16313858 | AATGGGCCCTTTCCA[A/C]TTAAGATGCAATGAA | 54455 |
rs550694013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16269909 | TCTGTCACCCAAGCT[A/G]GAGTGCAGTGGCTCA | 54455 |
rs550744151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16339277 | TATACCATTACTTAT[C/T]GACACAATGTCACAC | 54455 |
rs550798499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16267445 | CCAGTAAGACTACAC[C/T]ATCCTAGAAGACAGG | 54455 |
rs550808343 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16291382 | GGACTTTTTTTTTTT[A/T]AATTTATTATTTTAT | 54455 |
rs550811493 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16318159 | GTGCAGTGGCTCATG[C/G]TGTAATCCCAGAACT | 54455 |
rs550829760 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16353201 | GTCAAAGGCTTCAGT[C/G]TAAACTCTGTAAGCC | 54455 |
rs550852631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16275727 | TAAAAGGACAAAGGA[A/G]GCCAGGAGTGGTTGC | 54455 |
rs550860093 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16295923 | TACCAAGGCATGCTG[A/G]TTGGAGCCGACTAGA | 54455 |
rs550916297 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16325660 | ATATACTTTCTTTTT[G/T]TTGTTGTTTTGTTTT | 54455 |
rs550984963 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16269089 | ACTGGGATTACAGGC[C/G]TGAGCCACCGCACCT | 54455 |
rs551105501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16254473 | TCTCTAACCCTCAAG[A/G]GACCAACATGACGAG | 54455 |
rs551186003 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16322042 | AGGCGTGGTGGCAGG[C/T]GCCTGTAATCCCAGC | 54455 |
rs551210296 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16278309 | TGCAGTGAGCCGGAG[A/T]TCACGCCATTGCACT | 54455 |
rs551251568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16348059 | TAAGCTATATTATAA[A/G]CTTAATGCTGGACAA | 54455 |
rs551255585 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16300936 | CAGAGTGTTGTTCTG[C/T]CACCCAGGCTAGAGT | 54455 |
rs551276461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16276125 | GGTGGCTCACGCCTG[C/T]AATCCCAGCACTTTG | 54455 |
rs551289343 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16270926 | CAGTGTGACATATGG[G/T]GATAAGTGCCAAGGG | 54455 |
rs551380917 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16328434 | TATATTGGCATTGAA[C/T]GATTAAGTAAATAGT | 54455 |
rs551409895 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16291816 | AGCTAGGACTACAGG[A/C]ACATGCCATCATGCC | 54455 |
rs551431249 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16247618 | CATGGTTTTCAGCTG[C/T]TGCTGTAAAACTCGA | 54455 |
rs551441081 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16285428 | ATAGGCAGGCGCCAC[A/C]ATGCCCAGCTAATTT | 54455 |
rs551443617 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16295094 | TATTACCCTTTAAAA[C/G]AAGGTCCAGAGGAAA | 54455 |
rs551472018 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16249666 | CCTACTGGCCCCCTA[C/G]TGACACCAGGGAAAG | 54455 |
rs551478602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16252146 | TGAGAAATGCCAAAG[A/G]AGCTATGGCTAATGT | 54455 |
rs551495894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16314998 | GATACTTCAGTATTC[A/G]AGCTGTTCATTAAAC | 54455 |
rs551511503 | in-del | -/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16316188 | AAAAAAAAAAAAAAA[-/G]AAAGAAAGAAAAGAA | 54455 |
rs551529477 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16302270 | AGGGCAGGCCGGGTG[C/T]GGTAGCTCAACGCCT | 54455 |
rs551554184 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16263959 | GGGATTAGAGGTGTG[A/T]GCTACCACACTTGGC | 54455 |
rs551558102 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16300190 | CCACTAGAATGTGCT[A/G]TACAGTTACAGCTCA | 54455 |
rs551592709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16263519 | CTGAGGTCAGAAGTT[C/T]GAGACCAGCCTGACC | 54455 |
rs551686373 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16326615 | CTTGAGCCCAGGAGG[C/T]AGAGGTTGCAGTGAG | 54455 |
rs551719847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16271740 | CTCTTCATTTACCAC[A/G]TAAGTGTTTGGTTTT | 54455 |
rs551725021 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16310431 | AGCTATTTGGGAAGC[C/T]GAATTTGGAGGATTG | 54455 |
rs551743492 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16292130 | TAAACATTCAGGAGT[A/T]TGTATGTTTTGTCAA | 54455 |
rs551763844 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16309954 | TAATCCCAGCACTTT[C/G]GGAGGCCAAGGCAGG | 54455 |
rs551765198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16349785 | GAGAATCGCCTGAAC[C/T]GGAGAGGTGGAGGTT | 54455 |
rs551805041 | in-del | -/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16306022 | TTTTATACAAGTTTC[-/T]TTTTTTTTTTCTTTT | 54455 |
rs551809461 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16329884 | AACCAAGGAGGCAGA[C/G]GTTGGAGTGAGCCAA | 54455 |
rs551950035 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16336031 | CACTGAACACCTCCT[A/G]GGTTCAAGCGATTCT | 54455 |
rs551950523 | snp | A/G | | | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16354036 | TCTGTCGCCCAGACT[A/G]GAGTGCAGTGGCACC | 54455 |
rs551956436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16344657 | TACATTTTTAAACCT[C/T]CTTATACATACATAG | 54455 |
rs551969114 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16303401 | TGCCCCTTGCCTACT[G/T]CATGTTTATACTGCT | 54455 |
rs551976465 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16308398 | CAAGGCAGGAGGATC[A/G]CTTGAGCCCAGGAGT | 54455 |
rs551996715 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16287651 | AGGCTGGTCTTGAAC[G/T]CAAGCCATCCTGGCC | 54455 |
rs552003176 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16279036 | CTGGGTCGGCCTCCC[A/G]AAGTGCTGGGATTAC | 54455 |
rs552026424 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16248714 | CGAACAGTCTTTGCC[A/G]AGCAAGGATTGGCAA | 54455 |
rs552028278 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16352035 | GAGAGGGGGTGGGTT[A/C]GCTCCCAACCCAAGG | 54455 |
rs552032832 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16301688 | AAAAAAAAAAACAAC[A/C]AAAAAAAAAGAAACG | 54455 |
rs552047411 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16316951 | ACCACAGGTTATATA[C/T]ATATAAATAAATCTC | 54455 |
rs552072817 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16342153 | TGTAATCCCAGCACT[A/T]TGGGAGGCCAAGACG | 54455 |
rs552086838 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16308932 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 54455 |
rs552106993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16351072 | AATTCTAAATGATGG[C/T]ACTTCCCCCAAATTT | 54455 |
rs552157992 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16317454 | CAAAACTTAGCCAGG[C/T]TTGGTGATGCATGTG | 54455 |
rs552199316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16258969 | GGCCACGAACTCCTG[A/G]CCTCAAGCGATCCTC | 54455 |
rs552279693 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16274854 | CTCAGCCTCCCACAG[A/T]GCTGGGATTACAGGC | 54455 |
rs552308321 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16324923 | ATTGTAACTTAAACT[G/T]ATATCCTTTGCCACT | 54455 |
rs552311326 | snp | C/T | 8.27712e-05 | 0.00643263 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251126 | GGGGCCTTTGGAGGA[C/T]ATCGCTTTGATGGCT | 54455 |
rs552327405 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16277724 | CGAGATTCTGTCTCA[-/A]AAAAAAAAAAAAAAA | 54455 |
rs552335123 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16337625 | CAGTGGCTCACGCCT[C/G]TAATCCTAGCACTTT | 54455 |
rs552395837 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16267360 | GCTTCCTAAGACTTG[C/G]TTCTACCCAGGAGTG | 54455 |
rs552426827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16318237 | CAGCATGGCCAGCAT[A/G]GTGAAACCCGTCTCT | 54455 |
rs552489020 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16255251 | ATTTATTGGTCTGTG[A/T]TTAAGGGATTAAAGA | 54455 |
rs552503278 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16275029 | GTAAGCAGAAATATC[A/T]GCAATCCATTATTAG | 54455 |
rs552520483 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16326584 | AGCTACTCAGGAGGC[C/T]GAAGTGGGAGGATCA | 54455 |
rs552540360 | snp | C/T | 0 | 0 | intron-variant | FBXO42 | GRCh38.p7 | 1:16297230 | ATTATAGGTGAGAGC[C/T]AATGCGCCCAGCCCC | 54455 |
rs552589224 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16282289 | GGAGTGCAGTGGCGC[A/G]ATCTCGGCTCACTGC | 54455 |
rs552606430 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16268169 | TAGGGACTTTAAGAA[A/G]TGAAAACAATGTTAC | 54455 |
rs552607526 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16336772 | GTGAATCACCTAAGG[C/T]CAGGAGTTCAAGACC | 54455 |
rs552633888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16282005 | ATGCCTGGCCAAAGG[C/T]AGCTATTTCTACAAA | 54455 |
rs552640217 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16318837 | CAAAGACGGCCACTC[A/C]GGGGAATCTAGTACT | 54455 |
rs552671012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16325532 | ATAACAGATACCAGC[C/T]GCAGTTTTTAAAAAT | 54455 |
rs552703402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16311611 | TGGGTAACACATAAG[C/T]GCATGAAAATACGCT | 54455 |
rs552709143 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16275536 | AAGCAGGAGGATCGC[C/T]TGAGCCCAGGAATTT | 54455 |
rs552720249 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16345198 | GGAGACCAAGGCAGG[A/C]GGATCACGAGGCCAG | 54455 |
rs552728510 | snp | C/G | 0.000142263 | 0.00843274 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16253147 | AGTTGCATCATCTAT[C/G]ACAATCTGAGGAGGG | 54455 |
rs552851455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16289777 | ATCTCTACAAAACAA[C/T]ACAAAAATTAGCCAG | 54455 |
rs552856184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16289304 | AGCTATGCAGGAGGC[C/T]GAGGTGGGAGGATCA | 54455 |
rs552920018 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16281391 | ACCTCTCAAGGTCCA[A/C]GTACATCTCCTGGGA | 54455 |
rs552921466 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16344989 | CTGTAATCCTAGCTA[C/T]TCCGGAGGCTGAGGC | 54455 |
rs552931478 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16261414 | AAAGGCAAAATCTTT[A/C]CCTCTACTTTTTATC | 54455 |
rs552963966 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16351141 | GCAGAAGTAAAGCCA[A/G]TTTGTTACAAAAGAT | 54455 |
rs553005513 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16319035 | CTCTTGCTCCACACA[C/T]TCTACCCAGACCATT | 54455 |
rs553015085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16333986 | CGGTAAAAATAATAA[C/T]CCATCAGAAACTTCA | 54455 |
rs553015360 | in-del | -/CAT | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16321195 | AAAAACATCAAACCC[-/CAT]CATACCTTTGAGGGC | 54455 |
rs553018806 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FBXO42 | GRCh38.p7 | 1:16327000 | ACCATCTCTCTCTCA[C/T]CATCTCTCTCTATGA | 54455 |
rs553053860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16333264 | TAGAGATAGTTTCTA[C/T]TTTTCACCACTTCAT | 54455 |
rs553093917 | in-del | -/AAT/AATAATAATAAT | 0.0740033 | 0.178063 | intron-variant | FBXO42 | GRCh38.p7 | 1:16331428 | CAAAAAGAAAATAAT[-/AAT/AATAATAATAAT]AATAATAATAATAAT | 54455 |
rs553124905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16345601 | ACGCCTGTAATCCCA[A/G]CACTTTGGGAGGCCG | 54455 |
rs553130255 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16344633 | GAGCCACAGCACCCA[C/T]CCAGTTGTTACATTT | 54455 |
rs553194491 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16289564 | CCTTAGGCTACATCC[A/G]CAAAGGTCTGCTTTA | 54455 |
rs553214194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16304344 | GGCTGGTCTCAAACT[C/T]CTGACCTCAGGTGAT | 54455 |
rs553271231 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16331922 | AGGCATGGTGATACA[A/C]GCCTGTAATCCCAGC | 54455 |
rs553288609 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16305586 | AGGTGTGATGGGGCA[A/C]GCCTGTAGTCCTCAT | 54455 |
rs553323204 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16340190 | TCAAAAAAAAAAAAG[C/T]AAATTAAAAAAATTA | 54455 |
rs553390030 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16299073 | GCTGGAGTGAAATGG[C/T]ACAATCTTGGCTCAC | 54455 |
rs553391881 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16262378 | TAATTCCCTCTCGAT[C/G]ATCTTAAAGCAAAAT | 54455 |
rs553424669 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16313344 | AAAGAAAGAAAGAAA[G/T]AAAGAAAGAAAGAAA | 54455 |
rs553477696 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16263682 | GAGCCAAGATCGCAC[C/T]GTTGCACTCCAGCCT | 54455 |
rs553485210 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16348492 | TCACATGGTCAGGAG[C/T]TCGAGACCAGCCTGG | 54455 |
rs553510942 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16302364 | ACTATCCAAGACTGG[G/T]TAATTTATAAAGGAA | 54455 |
rs553550244 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16337322 | TTAAAATGTAGCTGG[C/T]ATCAACACTAGATGA | 54455 |
rs553562043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16268537 | GCTACAGGAAACAAG[A/G]AAGAACCACCACCTC | 54455 |
rs553592247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16256813 | TCTCACAACAATCCG[C/T]AGTTAGGCTATCCAT | 54455 |
rs553687651 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16334777 | AGGAGAAATGCTAAA[C/T]AGAAAGTACATAAAG | 54455 |
rs553697373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16309357 | GCTGGGATTATAGGC[A/G]TGAGCCACCGCGCCT | 54455 |
rs553703353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16254119 | TTCTTCCCCTACTTT[C/T]CCTAGAAGTCATCCT | 54455 |
rs553710977 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16276367 | CCCGGGCGACAGACC[A/G]ACACTCTGTCTCAAA | 54455 |
rs553738288 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16321664 | ATTGACATGTCTACT[C/G]AGAACACCTTTGTGC | 54455 |
rs553756025 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16262997 | ATTACAGGCGTGAGC[A/C]ACAACTTTGGTAATT | 54455 |
rs553764605 | in-del | -/A | 0.247337 | 0.249986 | intron-variant | FBXO42 | GRCh38.p7 | 1:16282981 | GTGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 54455 |
rs553788223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16278865 | CTCACCACAACCTCC[A/G]CCTTCTGGGTTCAAC | 54455 |
rs553827991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16270901 | TATAGCTTGCTGAGG[A/G]GAAGAAAGACAGTGT | 54455 |
rs553863797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16272617 | CAAGAGTATGCACAA[A/G]GGTAGAGGTGGAGAG | 54455 |
rs553893024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16301386 | AGTACAAGAAGGCTG[A/G]GTGCGGTGGCTCACA | 54455 |
rs553928502 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | FBXO42 | GRCh38.p7 | 1:16316523 | GGCAGATCACCTTAG[G/T]TCAGGAGTTCGAGAC | 54455 |
rs553936265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16307925 | TTATTTTGTGAATAT[C/T]GACAAACTGTTTCCA | 54455 |
rs553939694 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16278877 | TCCGCCTTCTGGGTT[C/T]AACCGATTCTCCTGC | 54455 |
rs553985639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16314578 | CTATGTTCACATTGG[C/T]TATTACTATTATCCC | 54455 |
rs554020809 | in-del | -/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16333438 | GGCAAATAGTGAGAC[-/C]CCCCCCCCCCATTTC | 54455 |
rs554047987 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16294302 | GGGTAGGAATGTACC[C/T]ACTGTAGAATCTTCC | 54455 |
rs554144951 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16286324 | AATTGACTCACAGTT[C/G]CGCATTGCTGGGAGG | 54455 |
rs554145128 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16296565 | TGAGGCAGGAGAATC[A/G]CTTGAACCCGGGAGG | 54455 |
rs554173437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16335631 | ACCACTTTGGGAGGC[C/T]GAGGCGGGTGGATCA | 54455 |
rs554189216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16330003 | ATTTCCAAATAATTC[A/G]TGTATGTACGTTTTC | 54455 |
rs554189270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16322431 | AAATACAAAAATTAG[C/T]TGGGCGTGCAGGCGC | 54455 |
rs554194696 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FBXO42 | GRCh38.p7 | 1:16260501 | GGTGTGAGCCACCGC[A/G]CCTGGCCCAATTACT | 54455 |
rs554208481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16323644 | TAAAAACAAAAATTA[A/G]CCAGGCGTGGTGGTG | 54455 |
rs554240931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16288311 | GGCACATGCCTGTAA[C/T]CCCAGCTACTGGGGA | 54455 |
rs554243561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16330824 | GTGGGCACCTGTAAT[C/T]CCAGCTACTCAGGAG | 54455 |
rs554256150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16264543 | CATTGAGTTCCCATC[A/G]AGCACGACAGGACCA | 54455 |
rs554295827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16344033 | ACAGAGTTTCACTCA[C/T]GTTGCCAAGGCTGGA | 54455 |
rs554344082 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16293692 | GAACTTAAGTTTTAG[C/G]GAAGCAAAATGCAGC | 54455 |
rs554350435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16323201 | AGGCGGAGGAATCAC[A/G]AGGTCAGGAGTTTGA | 54455 |
rs554355173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16280926 | TTACCAGGTGATTGT[A/G]AGCTTTGGTTTCCTC | 54455 |
rs554372581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16341893 | GGAGAATCGCTTGAA[C/T]CTGGGAGGCGGAGGT | 54455 |
rs554387798 | in-del | -/TT | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16306557 | GGTGTTGGGGGATAA[-/TT]TTTAGCCTTATGAAA | 54455 |
rs554433429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16295596 | TGGAGTTTCACCATG[C/T]TGGCCAGGCTAATCT | 54455 |
rs554449142 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16288623 | AACCTGAAACATAAG[A/T]CACCCTTGATTGGCC | 54455 |
rs554473363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16329400 | ATCAGCCTGGGCAAC[A/G]GGGTGAAACCCCGTT | 54455 |
rs554505872 | in-del | -/T | 0.48692 | 0.0798058 | intron-variant | FBXO42 | GRCh38.p7 | 1:16304114 | CCAGCCAAATTTGTA[-/T]TTTTTTTTTTTTTTT | 54455 |
rs554556217 | snp | A/G | 0.00716266 | 0.059414 | utr-variant-5-prime | FBXO42 | GRCh38.p7 | 1:16352437 | CACTCAAACGCCGCC[A/G]CCGCCGCAGCTGCTG | 54455 |
rs554645667 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16264354 | GGCACATAACCACTA[A/T]GGTGACATATGATGA | 54455 |
rs554699991 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16260201 | TACATCTATTATGTA[C/T]TATGCAGCTTTTTTT | 54455 |
rs554717672 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16324278 | ATATTAAAAACACAA[A/C]AAGAAAAAATATATT | 54455 |
rs554719657 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16272328 | GCAATGGCACGATCT[C/T]GGCTCACCGCAACTC | 54455 |
rs554727561 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16323651 | AAAAATTAGCCAGGC[A/G]TGGTGGTGTGCACCT | 54455 |
rs554732663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16253971 | CAAGTCACTTAATTT[C/T]CTCTAACTCTGACTT | 54455 |
rs554807434 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16268925 | GGGATTCTCCGGTCT[C/T]AGCCTCCCGAGTAGC | 54455 |
rs554847695 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16320556 | TCACCCAGGCTGGAG[A/T]GAAGTGGCACGATCT | 54455 |
rs554853153 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16258987 | TCAAGCGATCCTCCC[A/G]CCTCAGCCTCCCAAA | 54455 |
rs554872474 | snp | A/T | 4.95381e-05 | 0.0049766 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251220 | GGGGTATGCACACCA[A/T]TTGTCTGTTCAGGAG | 54455 |
rs554904860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16268701 | GGGCACAGCAGCTCA[C/T]GCCTGTAATCCCAGC | 54455 |
rs554906268 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250333 | TGGGAAGTTACTGAT[A/G]TTAGTCTATTCTCTA | 54455 |
rs554939798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16260781 | CATGGCTCACTGCAC[C/T]TCTGACCTCCTGGGT | 54455 |
rs554948025 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16329456 | AGGCGTGGCGGTGTG[C/T]GCCTGTAGTCCCAGC | 54455 |
rs554962251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16311715 | TCCAACTACTACTAC[A/G]AATGCTGGTGAGAAT | 54455 |
rs554994267 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16275904 | CCAGCTACTCGGGAG[C/G]CTGAGGGAGGAGAAT | 54455 |
rs555022652 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16276343 | CGAGATCACACCACT[C/G]CACACCAGCCCGGGC | 54455 |
rs555122725 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16286417 | AGCAGGACGGAATGA[A/G]TGCAAGCAGGGGAAA | 54455 |
rs555128224 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16304498 | TTGTGTTTGCTGAAC[A/G]TGTATTATGTTAAAT | 54455 |
rs555167524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16346249 | GGAAACATTTGAAAG[C/T]GCGTTTACCCCCATA | 54455 |
rs555193273 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16281500 | TTTGAGATGGAGTCT[C/T]GCTCTGTCACCCAGG | 54455 |
rs555244119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16282445 | TGGCCAGGGTGGTCT[C/T]GAACTCCTGATCTCA | 54455 |
rs555248978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16273832 | TGCAGTGAGCCAAGA[C/T]TGTGCCACTGCACAC | 54455 |
rs555345861 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16292625 | TAAACTTGATGGTTT[A/T]AAAAAAAAAAGTCTT | 54455 |
rs555350879 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16344101 | CTCCCAGGTTTAAGC[A/G]ATTCTCCTGCCTCAG | 54455 |
rs555377717 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16326402 | AAAATTTCTTCTTGA[G/T]GCCAGGTGCAGTAGT | 54455 |
rs555381750 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16319474 | TGATAATCAGCAAAT[G/T]GGTGGCTACTTGGAA | 54455 |
rs555395787 | snp | A/G | 0.148326 | 0.228391 | intron-variant | FBXO42 | GRCh38.p7 | 1:16313374 | AGAAAGAAAGAAAGA[A/G]AAAAGAAAGAAAACC | 54455 |
rs555511597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16291014 | CTATCAAGACTCTCC[A/G]CTCCCAACCAAAAGT | 54455 |
rs555527792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16339460 | TGGGACTACAGGTGC[A/G]TGCCACCACGCCCAG | 54455 |
rs555540529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16320070 | ATTCCTATCCTAAAA[C/T]GTACAGTCGCCGAGC | 54455 |
rs555543805 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16328575 | CTCATGTTTAAATAG[A/T]TACAGATGGTTACAT | 54455 |
rs555563706 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | FBXO42 | GRCh38.p7 | 1:16337693 | TTCAAGACCAGCCTG[A/C]CCAACATGGTGAAAC | 54455 |
rs555580805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16334521 | CAGTGATATGGTCTA[C/T]GTTAAACAGTCCACT | 54455 |
rs555600387 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16298727 | GTTGGCCAGGCTGGT[C/G]TCGAATTCCTGACCT | 54455 |
rs555620109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16283073 | AACCCACAGTTTAGG[C/T]AAGCTTCTCAGGTGA | 54455 |
rs555665332 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FBXO42 | GRCh38.p7 | 1:16325783 | GGCATGCGTCACCAC[A/G]CCCAACTAATTTTTG | 54455 |
rs555678878 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16319585 | CAAAAGCAGAGAAGA[C/G]TATTATAATGGGTTT | 54455 |
rs555691143 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16349344 | CCCAGCCATACTATA[A/T]GCAACTTCAGACCAA | 54455 |
rs555700890 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16314272 | ATATTTTAAAAAGTA[A/T]AAGATGTATATAGGG | 54455 |
rs555753971 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16247137 | GCCAACACCTAAAGT[C/T]TGCTCTCATTTGACA | 54455 |
rs555792912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16255572 | ACTCCTGACCTCAGG[C/T]GATCCACCCACCTTG | 54455 |
rs555796780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16340363 | CACTCTTGTTGCCTA[A/G]GCTAGAGTGAAATAG | 54455 |
rs555809767 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16270960 | AAAAAAAAAACAAAA[C/G]AAGAGGAAAAGGAGT | 54455 |
rs555813695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16343306 | GCCAACACTTTAGGT[C/T]AAGGCAGGTGGAGGA | 54455 |
rs555816983 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16306895 | TACATAACTCAGGAA[A/G]GTTTGTTTTCTTTTT | 54455 |
rs555876715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16327996 | GTGACCCACTTTGCC[C/T]AGCCAGGACAGTCTG | 54455 |
rs555878925 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16350194 | AATCTGGAGAGCAAA[A/T]GATGTCATGGATGTC | 54455 |
rs555881959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16257507 | AAACACTTTGGCTTA[C/T]GCTGGAAAACTTTAG | 54455 |
rs555894394 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16289409 | AAGATTGTCTCTTTA[-/A]AAAAAAAAAAAAAAA | 54455 |
rs555902614 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16308563 | GGAGTGCAGTGGCAC[C/G]ATCCCCGTTCACCAC | 54455 |
rs555917939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16321716 | TTTTTTTTTAAAGAT[A/G]GGGTTCTGCTCTGTC | 54455 |
rs555937735 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16323154 | CCAGGCACAGTGGCT[C/T]ACGCCTGTAATCCCA | 54455 |
rs555940024 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16354288 | TCTGGGATTACAGGT[A/G]TGAGCCACGGCGCCT | 54455 |
rs555945946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16306219 | AGATGGGGTTTCACC[A/G]TCTTGGCCAGGCTGG | 54455 |
rs555987468 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16340973 | TATAAAAAATCAGCA[G/T]TAAAGCATTATTTAC | 54455 |
rs556090727 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16334451 | AAAAACAGACTGATT[A/C]TACAGATAAGACTAA | 54455 |
rs556095376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16265330 | TCCCAACCTCAGGTG[A/G]TCCTCCCGTCTTGGC | 54455 |
rs556133243 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16347683 | AACATGTTGAAACCC[C/T]ATCTTTACTAAAAAT | 54455 |
rs556133311 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16278026 | CAGCCTGGGTGATGG[A/C]GTGACACCCTGTATC | 54455 |
rs556155121 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16256954 | ACACGTCTTTTATTA[G/T]TAACAGAGAAATATG | 54455 |
rs556195951 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250116 | ATAAAAGGCAAGAGG[C/G]GGCCAGGCACTGGCA | 54455 |
rs556195989 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16335683 | CCAGCCTGGCCAGCA[A/T]GGTGAAACACCATCT | 54455 |
rs556214423 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16302418 | CCACATGGCTGGAGA[C/G]GCCTCAGGAAACTTA | 54455 |
rs556256913 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16265898 | ACAGGTGTCTTAGGC[A/T]ATAATAGCCAAATGT | 54455 |
rs556285879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16294457 | AACTACAGTTCTCAC[A/G]ACTCTGTGTTTCTGT | 54455 |
rs556320847 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16332215 | GTAATCCCCTCTTTG[A/C]CACCTTTGATAAATT | 54455 |
rs556325883 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16272793 | GCTTTTCCTGATGTT[A/C]TAACTTCTAGCCTTT | 54455 |
rs556378751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16310052 | TAGAAAAAATTAGCC[A/G]GGTGTGGTGGTGGAT | 54455 |
rs556457414 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16263778 | AAACAAAACAAAACA[A/G]AAACAAAAAACCCAC | 54455 |
rs556478597 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16273603 | AAAAAAATGAGGGCC[A/G]GGCATGGTGGCTTAT | 54455 |
rs556507781 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16290219 | AGGAACTAAAGACAA[G/T]ATTTCACTGGGAAAT | 54455 |
rs556522316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16271855 | CTCAATAGTCCTCTG[C/T]AGGCTGGGCGCAGTG | 54455 |
rs556563631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16279620 | CTAATGATAAACATA[A/G]TAGTCAAATAGCTTA | 54455 |
rs556579619 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16308800 | CCCAGGCTGGAGTGC[A/G]TGGTGCAATGTCAGC | 54455 |
rs556616926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16316575 | ATCCCATCTCTACTA[A/G]AATACAAAAATTAGC | 54455 |
rs556617167 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16323558 | TCCCAGCACTTTGGG[A/T]GGCTGAGGTGCGCGG | 54455 |
rs556638283 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16278657 | CCACTAGACACATGA[C/T]AGTAAGCTTCATTAA | 54455 |
rs556653412 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16281548 | AACATGGTTCACTGT[C/G]ACCTCTGCCTCCCAG | 54455 |
rs556656312 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16289022 | CTGAGTCTTGTCAAT[A/C]TTGATGGCCTTCTGT | 54455 |
rs556664875 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16306933 | TTTGAGACAGAGTCT[C/T]GCTCTGTTGCCTAGG | 54455 |
rs556669619 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | FBXO42 | GRCh38.p7 | 1:16331277 | AATTAGCCGGGCATG[A/G]TGGCGGGCGCCTGTA | 54455 |
rs556689889 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16259033 | GCATTACCCACCTCA[C/T]CCAGTCAGAAATCTT | 54455 |
rs556706962 | snp | A/C | 0.0741063 | 0.177655 | intron-variant | FBXO42 | GRCh38.p7 | 1:16296663 | TCAAAAAAAAAAAAA[A/C]AAAAACAAAAACAAA | 54455 |
rs556731463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16259715 | AGGTTGCAGTGAGCC[A/G]AGATTGAGCCACTGC | 54455 |
rs556765361 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16287298 | ACCCATCAAGTCCTT[C/G]TTCTAATGTCGCCTT | 54455 |
rs556774361 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16259070 | GAAGAGTTATCACAT[C/T]AATCTGAAGTGCTGA | 54455 |
rs556799922 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16295363 | AAATTAAACCTGAAG[A/C]ACAAATCAATAAATG | 54455 |
rs556802078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16286522 | CCAATTACCTCCACC[C/T]GGTCCTGCCCTTGAC | 54455 |
rs556831431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16297365 | AAAGCAGTATGTTTA[A/G]TGCCTTAAACCCCAT | 54455 |
rs556857065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16323236 | AGCCTGGCCAACATG[A/G]TGAAACCCCATCTCT | 54455 |
rs556884418 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16303190 | CTGAAAAGGCAAGCC[A/C]GGTCCTTGAAAGGCA | 54455 |
rs556925545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16269030 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCG | 54455 |
rs556981145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16338708 | GGGTGGCATATAAAC[C/T]TAGCTTCCCCACTGA | 54455 |
rs556987443 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16322916 | ATTTCAACATGGGAA[A/T]GAAACTGCTATGCAT | 54455 |
rs557007271 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16340069 | ATAGTCCCAGCTCTT[A/G]GGAGGCTGAGGCAGA | 54455 |
rs557043990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16339571 | CCGCCTCAGCCATCC[A/G]AAGTGCTGGGATTAC | 54455 |
rs557056673 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16343986 | AACAAAAAAAGAAAA[C/T]TGCAAAGGGATCTTT | 54455 |
rs557068092 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16331848 | CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGACC | 54455 |
rs557112350 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16253488 | ATGACCCATTAGAAG[C/T]TGAAAAATAAATACC | 54455 |
rs557119733 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16296859 | TTGACTCATCCAATG[A/C]CACTACTATAATCAC | 54455 |
rs557122489 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16319504 | AGGACTGGAGTGGCT[G/T]AAGTCCACCTGGTGG | 54455 |
rs557125927 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16300860 | GCTTGCATGATTAGC[C/T]ATGCACACATTCACC | 54455 |
rs557147181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16332690 | GGATTACAGACATGT[A/G]CCACCATGCCCAGCT | 54455 |
rs557152510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16318396 | GCACTCCAGCCTGGG[C/T]GACAGAGCAAGACTC | 54455 |
rs557192787 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16262235 | GCTATGCTGCCCAGT[C/T]TGGTCTTTAACTCCT | 54455 |
rs557214949 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16346733 | AAGTTACTAAGCTAA[A/C]TTACTGTACTGAACA | 54455 |
rs557229456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16251980 | GCTTTGTGTGACATA[C/T]GCTATCATTAGAGAT | 54455 |
rs557252215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16303811 | AGTGCAGTGGCGTGA[C/T]CTCGGCTCACTGCCA | 54455 |
rs557264812 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | FBXO42 | GRCh38.p7 | 1:16319159 | GGATTTGGCGGGGGG[G/T]GGGGAAGGAAACGAA | 54455 |
rs557267273 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16289343 | CAGGGGTTTGAGGCT[A/G]TAGTCAATTAATTAT | 54455 |
rs557293146 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16298919 | TTGTTACGTCTCCCA[G/T]TTCCTCACAGATAAC | 54455 |
rs557312285 | in-del | -/A | 0.0599851 | 0.162463 | intron-variant | FBXO42 | GRCh38.p7 | 1:16346692 | GACTCCGTCTCGGGG[-/A]AAAAAAAAAAAAAAC | 54455 |
rs557321971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16262629 | TGGGAGGTGGAGGTT[A/G]CAGTGAGCCCAGACC | 54455 |
rs557341366 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16353365 | ACGGGAAGCAGGACA[A/T]GAGACATGCCTCATT | 54455 |
rs557346723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16337813 | TGCTTGAACCCAGGA[A/G]GCAGAGGTTGCAGTG | 54455 |
rs557366780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16304629 | TCAGATGTTTAAAAC[A/G]CTAAGCATAACACCT | 54455 |
rs557447940 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16305653 | GGGGAGGTGGAGGCT[A/G]TAGTAAGCTGTGATT | 54455 |
rs557492844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16321183 | TTACACCCTCCACAA[A/G]AACATCAAACCCCAT | 54455 |
rs557498316 | in-del | -/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16340324 | AACCTTTGGTAGTAC[-/T]TTTTTTTTTTTGAGA | 54455 |
rs557513197 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16277087 | AAAGATCTGTGAGTA[A/G]AACTGGATTGTCTCA | 54455 |
rs557519148 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16334015 | CAAAAGGCTATATTC[C/T]GTACCATTTCTATGA | 54455 |
rs557548419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16267705 | AAAGTTACTGATTGA[C/T]ATCAACATTCACTGG | 54455 |
rs557659452 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16340845 | TGAGGAAAGTGAGGT[C/G]AGAAAACCTAAGTGG | 54455 |
rs557683856 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16278080 | TCCACATCCAGGCCA[G/T]GCGTGGTGGCTCATG | 54455 |
rs557685767 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16286249 | CATCTGGATTAGTCT[A/G]TTCTCACAGTGCTAT | 54455 |
rs557764013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16269651 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 54455 |
rs557771751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16285744 | AAACGCTTTCCTCAT[A/G]TGCTGGCTTCCCAGA | 54455 |
rs557881580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16306999 | CAGGTTCAAGTGATT[C/T]TCCTGCCTCAGCCTC | 54455 |
rs557918505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16314494 | CATCTATAAAATGCA[A/G]GATCTTCTAGTCAGA | 54455 |
rs557927673 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16256566 | CCACTGATTTAAGGC[A/C]TTTTCTTCCAGATTT | 54455 |
rs557929056 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16322260 | CTATTTATTTGGCCC[A/T]GTAGTATCTTTTTCT | 54455 |
rs558013777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16329277 | CCATAAAATAAATTG[A/G]TATTGGATCAAAACC | 54455 |
rs558024244 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16345074 | ATTGTACTCCAGCCT[A/G]AGAGACAGAGTGAGA | 54455 |
rs558027361 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16291699 | TTTTTTGAGACAGGG[A/T]CTCCCTCTTTCACTC | 54455 |
rs558040530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16301232 | CTTCACCTGACTTTT[C/T]TGTCCCAGACTTTTC | 54455 |
rs558041397 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16320152 | ATCACCTGAGGTCAG[C/G]AGTTCAAGACCAGCC | 54455 |
rs558049379 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16276392 | CTCAAAAAAAAAAAA[A/G]AAAAGAAAAGAAAAG | 54455 |
rs558116668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16328735 | AGTTCTTTCTAATAC[C/T]GTTCTCCAATAAAAG | 54455 |
rs558150835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16293553 | AGACTGGACCACCAC[C/T]CTCCTACCCTCCAAA | 54455 |
rs558166522 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16335542 | TATTTCGCTGTAGTA[C/T]TAAACTTCATGATGC | 54455 |
rs558195157 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16284142 | AGAATTAAGGTGTTA[C/T]CTTCAGACAATACTA | 54455 |
rs558199726 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16336857 | GGGTGTGGTGGCAAA[C/T]GCCCGTAATTCTAGC | 54455 |
rs558201440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16330162 | TCATTCCTGCATACC[C/T]TGGGCAAATAAAACT | 54455 |
rs558240669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16295516 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 54455 |
rs558276203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16321894 | CATCATTAGGCCAGG[C/T]GTGGTGGCTCACGCC | 54455 |
rs558277913 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16302512 | CAGGGGAAACTGCCA[C/T]CTTTTTTTCTTTTTT | 54455 |
rs558283325 | in-del | -/A | 0.309154 | 0.242901 | intron-variant | FBXO42 | GRCh38.p7 | 1:16310194 | GCAAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 54455 |
rs558287809 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16350291 | AATGATGAGCCACCA[C/G]GATGTTTTACTGCAT | 54455 |
rs558348325 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16347862 | GCTGTGGTAGTGGGC[A/G]CCTGTAGTCTCAGCT | 54455 |
rs558348341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16347732 | CAGTGGCTCACGCCT[A/G]TAATCCCCACACTTT | 54455 |
rs558354681 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16315848 | GTCTTGCAAAAAGTA[A/G]TAACATTCTGAGAAT | 54455 |
rs558378188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16341234 | GATAAACCAAAACCA[A/G]ATAAATATTAGAATG | 54455 |
rs558390567 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16307719 | AAAAAATGAAATACT[A/T]AGATATAACAAAATA | 54455 |
rs558427492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16309230 | GCGCCACCATACCCA[A/G]CTAATTTTTTTTTTC | 54455 |
rs558459961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16316443 | TCCACTTACAAAATA[C/T]AGTAGTTCTTGGTTG | 54455 |
rs558459998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16308584 | CGTTCACCACAATCT[C/T]TGCCTCCTGAGCACA | 54455 |
rs558463408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16264388 | AAATACTGCTCCTGC[A/G]AGAACACTTATAAAA | 54455 |
rs558470331 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16338763 | CATAATACATTTTAA[C/T]AAGATGCTGTGATGG | 54455 |
rs558495508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16341800 | ACATGGAGAAAACCC[C/T]GTCTCTACTAAAAAT | 54455 |
rs558499762 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16271925 | GGGTGGATCACCTGA[A/G]GTCAGGAGTTCGAGA | 54455 |
rs558594576 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16264686 | AAGGCCTCCTAAATC[A/G]CACAGCAGATATGAT | 54455 |
rs558658280 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16293159 | CTTTATTATTCCAAT[A/G]GTTTTTGTGGAGACT | 54455 |
rs558711107 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16266101 | AATAATCAAACAAGA[C/T]AGAACTTTTGAAAGA | 54455 |
rs558757419 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16315533 | TAATTTCGTTTCCAC[A/T]CTCAGTGTGAAATCT | 54455 |
rs558817724 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16264957 | CTAGTTTGATTTCTA[C/T]GCCACTTTCCCACAA | 54455 |
rs558920240 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16247598 | ACACAGTTCCTAGAA[C/T]AGTTCATGGTTTTCA | 54455 |
rs558920995 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16272419 | CATGCACCACCACGC[C/T]CAGCTAATTTTGTAT | 54455 |
rs558941435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16274246 | AAGAGCTGGAGCTGC[A/G]GTGAGCTATGATAAT | 54455 |
rs558946863 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16317239 | CCTGGCCAACACAGT[A/G]AAACTCCATCTCTAC | 54455 |
rs558953989 | in-del | -/AAACAAACAAAC | 0.00836305 | 0.0641217 | intron-variant | FBXO42 | GRCh38.p7 | 1:16347515 | AGAGACTTCCTCTCA[-/AAACAAACAAAC]AAACAAACAAACAAA | 54455 |
rs558960921 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16274598 | CCCCCGTTTTTTTTT[G/T]TTTTTTTTTTTTGAG | 54455 |
rs558964083 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16321254 | ATGCCAAGGAGAACA[C/T]ACATGGGTGAGCTCA | 54455 |
rs558973399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16304053 | CAGGTGATCCGCCCG[C/T]CTTGGCCTCCCAAAG | 54455 |
rs558975205 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16312081 | GAAATGGAGGAAGCC[A/G]GGCACGGTGGCTCAC | 54455 |
rs558982363 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16333605 | AAATTAATTAAAATA[C/T]GAAAAAATAAAATCC | 54455 |
rs559107004 | in-del | -/TTTG | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16336353 | TTCTTGCTGCCCTTT[-/TTTG]TTTGTTTTTGTTTTT | 54455 |
rs559128585 | snp | A/C | 0.105214 | 0.203807 | intron-variant | FBXO42 | GRCh38.p7 | 1:16310998 | AAACAAACAAACAAA[A/C]AAACTCAACATTAAT | 54455 |
rs559150211 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16280817 | CGAAAACTACTCACA[G/T]CATGGCTTAGTAGAA | 54455 |
rs559237154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16279833 | ACAGTGAAAAATCAT[A/G]TTGACAATGGTTTTT | 54455 |
rs559252313 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16266980 | TTTACAGGCAATACT[A/T]CGTAAGGGCAACAAC | 54455 |
rs559275405 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16348721 | AATAAAAAAGAAAAA[G/T]AAAGTTTAGTGTAAT | 54455 |
rs559278581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16318094 | TTGTAAAAAATTTAC[C/T]GAGCTGAATACTCAC | 54455 |
rs559309947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16325567 | AACTCATTAGTGTGC[C/T]ACCCAATTAAGATTC | 54455 |
rs559313951 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16332805 | CTCGGCCTCCCAAAG[G/T]GCTGGGATTACAAGT | 54455 |
rs559336696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16320188 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 54455 |
rs559348174 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16332333 | GGCACATTGTTATTA[C/T]TACCATTGCTATAGT | 54455 |
rs559392814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16323831 | AAAGAATAAGGGACA[A/G]GAAGGAGGAGCAGAG | 54455 |
rs559416382 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16260397 | GTATTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 54455 |
rs559500018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16288490 | AAATGTCAAACTCTC[A/G]TAACAATGAATTACT | 54455 |
rs559509366 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16288088 | GAGATGGAGTGAGCC[A/G]AGATCATGCCATTGC | 54455 |
rs559569048 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16347035 | TAGGCATGAGCCACC[A/G]CACCCGGCCTGTCAG | 54455 |
rs559582909 | in-del | -/AAAC | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16311014 | AAACTCAACATTAAT[-/AAAC]AAACAACCCAATTAA | 54455 |
rs559656182 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16325406 | GTCTATGTTTTGACC[A/G]AAAAAAAAGCCTAGA | 54455 |
rs559711866 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | FBXO42 | GRCh38.p7 | 1:16246449 | CCTGGTCTAAGTGAT[C/T]CTCCTGCCTCAGCCT | 54455 |
rs559735215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16345224 | GCCAGGAGTTCGAGA[C/T]CAGCCTGGCCAACAT | 54455 |
rs559748602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16283393 | TTCTGTGGGGAGAAT[A/G]TGGTGGGAAAATCAA | 54455 |
rs559756170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16275552 | TGAGCCCAGGAATTT[A/G]AGGCTGCAGTGAGCT | 54455 |
rs559803841 | in-del | -/AA | 0.178465 | 0.239547 | intron-variant | FBXO42 | GRCh38.p7 | 1:16326684 | ACCAAACCCTGTCTC[-/AA]AAAAAAAAAAAAAAA | 54455 |
rs559971807 | in-del | -/AAAGAAAG/AAG/AAGAAAGAAAGAAAG | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16350757 | CAAAAAAAAAAAAAA[-/AAAGAAAG/AAG/AAGAAAGAAAGAAAG]AAAGAAAGAAAGAAA | 54455 |
rs559997811 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16352967 | AGAAAACGATCACTT[A/C]TTTGCCCGGAGTCAC | 54455 |
rs560004957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16341373 | TTGGGAGGCCGAGGC[A/G]GGCAGATCATGAGGT | 54455 |
rs560020033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16252712 | GGAGAGGATAAATAA[C/T]ACATATCCACAACTT | 54455 |
rs560020971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16298210 | CAGCCTGGGCGATAG[A/G]GCAAGACTCTGTCTC | 54455 |
rs560029419 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16291673 | AAGCGAGAGCCACCA[A/C]GCCCAGGCTATTTTT | 54455 |
rs560033768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16254294 | GGAAATAGACACTGG[C/T]TAAGCTACAGTTTTC | 54455 |
rs560041320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16269776 | GTGATCCGCCTACCT[C/T]GGCCTCCCAAAGTGC | 54455 |
rs560045649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16340611 | GGCGTGAGCCACTGC[A/G]CCCGGCCAACCCTCT | 54455 |
rs560069386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16320221 | AAAAAACTAGCTGGG[C/T]GTGGTGGCACATGCC | 54455 |
rs560105827 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16347137 | ATATATAAATACACT[G/T]ATCTGTGTGTGTGTG | 54455 |
rs560162105 | snp | G/T | 0.0228947 | 0.104514 | intron-variant | FBXO42 | GRCh38.p7 | 1:16271265 | TGTGTGTTGGTGTGT[G/T]TGTGTGTGTGTGTGT | 54455 |
rs560190540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16284594 | CCCAGCACTTTGGGA[A/G]GCCAAGATGGGCAGA | 54455 |
rs560220389 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16292086 | GGGAGTAACTAGATT[C/G]TTTGAGACATTTTGT | 54455 |
rs560225856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16313749 | TGTTCTCTGTTATAT[C/T]TCTGGCTGCCTTGTT | 54455 |
rs560246711 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16262069 | ATTTGGCATATTTAT[G/T]GCAAATTGGATACTT | 54455 |
rs560271460 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16312866 | GTGGCTCGATCTTGG[C/T]ACACTGCAACCTCTG | 54455 |
rs560296020 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | FBXO42 | GRCh38.p7 | 1:16276394 | CAAAAAAAAAAAAAA[A/G]AAGAAAAGAAAAGAA | 54455 |
rs560439572 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16306313 | TGAGCCACCGCGCCC[A/T]GCCTATAAGACAAGT | 54455 |
rs560531728 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FBXO42 | GRCh38.p7 | 1:16285122 | CTGTACTCCAGCCCC[A/G]CGACACTGCAAGACT | 54455 |
rs560537263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16322927 | GGAATGAAACTGCTA[C/T]GCATTTAAAAGCCAT | 54455 |
rs560537332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16330283 | CCCAGCACTTTGAGA[C/T]GCCAAGATGAGAGGA | 54455 |
rs560576625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16329632 | AATGAATATCCACAA[A/G]TTCATATTGATATAA | 54455 |
rs560581761 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16263479 | TTCTTTAAAAGCACA[C/T]GGCCGGCCAGGCGTG | 54455 |
rs560585635 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | FBXO42 | GRCh38.p7 | 1:16308749 | ATCTCTGTTTTTTTT[G/T]TTTTTTTTTTTTTGA | 54455 |
rs560586732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16321934 | AGCAATTTGGGAGTC[C/T]GAGGTGGGTGGATCA | 54455 |
rs560621706 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16339278 | ATACCATTACTTATC[A/G]ACACAATGTCACACT | 54455 |
rs560652636 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16323347 | CGCTTGAACCTGGGA[A/G]GCAGAGGTTGCAGTA | 54455 |
rs560762688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16301967 | AATTTGTCATATCCA[C/T]TTTTCAGACAAAGAA | 54455 |
rs560877313 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16279139 | AATTTTTAAGGATAT[C/T]CTGTGGTCTTCCTAC | 54455 |
rs560945841 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16345095 | CAGAGTGAGACTCCG[C/T]CTCAAAAAAACGACA | 54455 |
rs560949181 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16287428 | TATCTGTCTTCCTTC[A/T]TTTGAATGTAGTCTC | 54455 |
rs560965340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16336355 | CTTGCTGCCCTTTTT[C/T]GTTTGTTTTTGTTTT | 54455 |
rs561023088 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16286841 | AAAACCTGAAGAGTC[A/C]TCTTGATTGCTTTCT | 54455 |
rs561026241 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FBXO42 | GRCh38.p7 | 1:16352236 | CCCTCTGCGGCCCGG[A/G]GAGGAGGAGAGGCCT | 54455 |
rs561124560 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16297824 | GTGAGCCAAGATCCC[A/G]CCACCGCACTCCAGC | 54455 |
rs561126288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16337432 | CATATTATCAATTCT[A/G]AGATGAGGATAAGAT | 54455 |
rs561152207 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16294022 | AATGGAAACCCAAAT[A/G]TCCTTAGTCCTAAGA | 54455 |
rs561174362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16342003 | AGTTCTGGGCCAGGC[A/G]CAGTGGCTCATGTCT | 54455 |
rs561205717 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16349586 | TAATTCAGGGCCGGG[C/T]GCAGTGGCTCAAGCC | 54455 |
rs561220736 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16281298 | TGGAGATAATTATAG[G/T]ATCATCCTATTGAGT | 54455 |
rs561255574 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16261393 | TCAGATATCTTGACC[-/T]TTTAGAAAGGCAAAA | 54455 |
rs561259203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16288720 | CCCAGCACTTTGGGA[A/G]GCCAAGGTGGGCGGA | 54455 |
rs561263281 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16325915 | ACAGGCGTGAGCCAC[C/T]ACACCTGGCCGAAAA | 54455 |
rs561302014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16309766 | TTAGCCGGGTGTGGC[C/T]GGGTGCAGTGGCTCA | 54455 |
rs561367398 | snp | A/G | 8.28782e-05 | 0.00643679 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251481 | CCACCCACAGCTGCC[A/G]TTCCTGGAGACAAAC | 54455 |
rs561372099 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16265534 | ATTATCTAATTTAAT[C/T]ATTATAACCTTAAAA | 54455 |
rs561396228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16267810 | AACATCATTCTATGG[A/G]TCATTTATGAAATAT | 54455 |
rs561397218 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16297600 | GGCGTGGTGGCTCAC[G/T]CCAGTAATCCCAGCA | 54455 |
rs561401087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16298404 | TCCTAAAAAATGGGG[C/T]AATTTTGAAATGAGC | 54455 |
rs561430594 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16289362 | TCAATTAATTATGAT[C/T]GTGCCACTGCACTCC | 54455 |
rs561458665 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16295116 | CAGAGGAAAGCTATG[A/T]AAATTTTATTTCTGA | 54455 |
rs561513225 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16317369 | GTTGCAGTGAGCAGA[A/G]ATCACTCCGCACTCC | 54455 |
rs561516228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16274678 | CTCACTGCAACCTCC[A/G]CCTCCTGGGTTCAAA | 54455 |
rs561519872 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16303293 | CATGTTTCAGACTTG[C/T]AGTATTTCCCAACAG | 54455 |
rs561576027 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16298310 | CAAAAGGACAATTAC[C/T]GGAGCCACATTTTAA | 54455 |
rs561584454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16305634 | GGGAGGATCACCTGA[A/G]CCTGGGGAGGTGGAG | 54455 |
rs561609683 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16302810 | CCACTGCGGCCAGCC[A/G]AAACCGCCACTTTTA | 54455 |
rs561615570 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16247231 | GAGAGGCTACATGGG[-/A]ACGCAGGCCTGGAAA | 54455 |
rs561635894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16267242 | GGCCAATAATAATTA[C/T]AAGTCATTGCATTTA | 54455 |
rs561669185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16310244 | CATGCACCTGTAATC[C/T]CAGCTACTTGGGAGG | 54455 |
rs561720435 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16310050 | AATAGAAAAAATTAG[C/T]CGGGTGTGGTGGTGG | 54455 |
rs561733014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16319727 | ACCAGCCTGGCCAAT[A/G]TGGTGAAACTCCGTC | 54455 |
rs561788837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16346027 | AGGAGGCTTATGCTG[A/G]CCAAATTTCAGGGTC | 54455 |
rs561840962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16253547 | GCTTAGTGCATATTG[A/G]CATCTTACCTGACTC | 54455 |
rs561849772 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16324771 | CAGTGAGCCAAGATC[A/G]CGCAACTACACTCTA | 54455 |
rs561893676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16320309 | GAAGTTGCAGTAAGC[C/T]GAGATCATGCCACCG | 54455 |
rs561927455 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16281715 | CCAGGCTGGAGTGCA[A/G]TGGCAATCTTGGCTC | 54455 |
rs561930761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16318738 | AACTTCTGGAAGAAG[C/T]GCAGAAGCAGCAGGA | 54455 |
rs561965324 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16290647 | CAGTGAACCAAGATC[A/G]CACCACTGCACTCCA | 54455 |
rs561966031 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16325279 | CCTTTAAGACAAAAC[A/T]AAACTAAACTAAAAA | 54455 |
rs561966155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16318120 | CTCACGCACTTCTCT[A/G]AAGTTTGTCAAAATA | 54455 |
rs561985576 | in-del | -/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16346687 | GCTAGACTCCGTCTC[-/G]GGGGAAAAAAAAAAA | 54455 |
rs562076269 | in-del | -/A/AA | 0.00318978 | 0.0398085 | intron-variant | FBXO42 | GRCh38.p7 | 1:16259765 | GCAAGACTCTGTCTC[-/A/AA]AAAAAAAAAAAAAAA | 54455 |
rs562090120 | snp | C/G/T | 0.00755907 | 0.0610114 | intron-variant | FBXO42 | GRCh38.p7 | 1:16267548 | AGCTGAGATCAGGGT[C/G/T]GGCTCCAGCTACTTA | 54455 |
rs562146542 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16269805 | GCTGGTATTACAGGC[A/C]TGAGCCACCATGCCT | 54455 |
rs562171834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16313783 | CCAGGAAAGAACACA[C/T]TGAGACAACCCTCGC | 54455 |
rs562175729 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16254186 | TGAGCCACGTCTGCG[A/G]CCAGACACTAGTGCC | 54455 |
rs562179506 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16339200 | GAGCAGAGGAGAGGA[C/G]CTCCTTCCATCACAA | 54455 |
rs562218629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16333377 | CAGCAACTCAGGAGA[C/T]TGCCACCAGAGGATC | 54455 |
rs562256360 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16287609 | TTTTTATTATTTTTG[C/T]AGAGATGGGCTCTTG | 54455 |
rs562280945 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16346408 | CTAGAAAATAAGAGA[G/T]CGAGGCGTAGTGGCT | 54455 |
rs562377339 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16247395 | CCAACCAGGAATACC[A/G]CTTTTAAGGGGGAAG | 54455 |
rs562390806 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16307720 | AAAAATGAAATACTT[A/C]GATATAACAAAATAC | 54455 |
rs562401577 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16283543 | CGCTCTGTCGCCCAG[C/G]CTGGAGTGCAGTGGC | 54455 |
rs562415526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16332919 | CATGAATTTAACAAT[A/G]AGAAGAGTAGTGGCT | 54455 |
rs562422690 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16259455 | GCTTAAAGAAATTAT[-/A]AATGCAGTATAAGAA | 54455 |
rs562436912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16285917 | TCGTCACCCAGACTG[C/T]AGTGCAGTAGCGCAA | 54455 |
rs562440336 | snp | C/T | | | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16317278 | CAAAAATTAGCTGGG[C/T]GTGGTAGCGTATGCC | 54455 |
rs562453243 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16334982 | CCGTAATCCCAGCAC[C/T]GTGGGAAGCCAAGGT | 54455 |
rs562466536 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16335219 | GACTGTTTGAGGCCA[A/G]GAGTCCAGCTGGGGC | 54455 |
rs562470578 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16347980 | CCTGGCGACAGACCC[A/G]AGACTCCGTCTCAAA | 54455 |
rs562485928 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16293029 | CCAAATATTAATCAA[G/T]TTGCACTAAGTGCAA | 54455 |
rs562503396 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16334365 | GTGAACCCGGGAGGC[A/G]GAGCTTGCAGTGAGC | 54455 |
rs562521011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16301434 | TTGGGAGGCTGAGAT[A/G]GGCAGATTTCTTGAG | 54455 |
rs562563274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16314711 | AACACAGTGAAACCC[C/T]GTCTCTAGTAAAAAT | 54455 |
rs562602222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16293756 | AGACATTCACAGTAG[C/T]GGTTATAGAAAGGGA | 54455 |
rs562637609 | snp | G/T | 1.64806e-05 | 0.00287054 | missense, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16294806 | AAAGGTCGGATCCAC[G/T]CTTTGCTGTTTAGGT | 54455 |
rs562663714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16255329 | TCAGGAATACTGACC[C/T]TAACTTACTTTTTTT | 54455 |
rs562664606 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16255929 | ATCACTTTCAGCAGA[C/G]ATTTGTTGGGATAAT | 54455 |
rs562666224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16258577 | GCCCAGACTGGTCTC[A/G]AACTCATGGGTTCAA | 54455 |
rs562669100 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16302111 | AATGGAGGAAGGTAT[G/T]AATAGTATATTAGGG | 54455 |
rs562715037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16271600 | ACTACCTTTCTAATA[C/T]CCACTTGTACCACTC | 54455 |
rs562761813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16308868 | CCTGCCTCAGGTTCC[C/T]AAGTAGCTGAGATTA | 54455 |
rs562766177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16300825 | CATCAATCTGAAAAG[A/G]ACATTCTACATTAAT | 54455 |
rs562803245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16300136 | CCTTTTCACAAGTTC[C/T]CAACCTAAATAGAAA | 54455 |
rs562825248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16263924 | CAAGCGATTCTCCTG[A/G]CTCAGCCTCCCGAGT | 54455 |
rs562873565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16302147 | GAGAGGAAGAAAAGA[A/G]CTTAATATCTACGGC | 54455 |
rs562932662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16316605 | CCAGGTGTAGTGGCG[C/T]GTGCCTGTAATCCCA | 54455 |
rs562947995 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16278304 | GAGGTTGCAGTGAGC[C/T]GGAGATCACGCCATT | 54455 |
rs562964320 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16335992 | GCTGGAGTACAATGG[C/T]GCAATCTCGGCTCAT | 54455 |
rs563002650 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16310342 | CTCCAGCCTGGGTGA[C/T]GGAGTGAGGTTCCAT | 54455 |
rs563068152 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16279066 | CAGGCATGAGCCACC[A/G]CGCCCAGCCTAGACG | 54455 |
rs563111722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16287565 | GAGAGAAGAATTTAA[C/T]TGAACAGAAGGACTG | 54455 |
rs563134011 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16315959 | GCAGATCACCTGAAG[G/T]TGGGAGTTTGAGACC | 54455 |
rs563165724 | snp | G/T | | | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16353818 | CTCCCAAAATGCTTG[G/T]ATTACAGGCGTGTGC | 54455 |
rs563178322 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16273193 | AACCGGTAACCAGCA[A/G]GTGACAGGGCTCAAA | 54455 |
rs563179896 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FBXO42 | GRCh38.p7 | 1:16272149 | GACAGAGCAAGACTC[C/T]GTCCCAAAAAAAAAA | 54455 |
rs563223134 | snp | A/T | 0.021333 | 0.101051 | intron-variant | FBXO42 | GRCh38.p7 | 1:16288449 | AAATAAAAATAAAAA[A/T]AAAAATAATAATAAT | 54455 |
rs563223742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16322686 | GAGGTATAAATTAAG[A/G]TTAAGATTTTGAGAC | 54455 |
rs563290171 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16256302 | ACTCCTGGAGTGTTA[A/G]CAGCCAAAGCTGAAG | 54455 |
rs563324197 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FBXO42 | GRCh38.p7 | 1:16276354 | CACTGCACACCAGCC[C/T]GGGCGACAGACCGAC | 54455 |
rs563338008 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16323906 | AGTCATCCCACAGCA[C/T]GAGGGCTTCTGAGGC | 54455 |
rs563338220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16338992 | ATTTCTGTATTTTTA[A/G]TAGAGATGGGGTTTC | 54455 |
rs563338970 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16281121 | GCATGCACCATCACA[A/C]CTGGCTAATTTTGTA | 54455 |
rs563356153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16266197 | TTTTTTTAAAAAAAA[C/T]AGAAACATCTCTTTC | 54455 |
rs563374903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16345824 | CTGCACTCCCGCCTG[A/G]GCGACAGAGCGAGAC | 54455 |
rs563404797 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16287310 | CTTGTTCTAATGTCG[C/T]CTTCTCTCTGATTCT | 54455 |
rs563405480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16323405 | CCCAGGTGACAGTGC[A/G]AGACTCCGTCTCAAA | 54455 |
rs563442083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16330396 | GGGTGTGGTGGCAGC[C/T]ACTTGGGGGCTGGGG | 54455 |
rs563509585 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16343639 | CCAGCCTCGCCAAGA[C/T]GGTGAAACCCCATCT | 54455 |
rs563529324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16331537 | AGGTGGGTGGATCAC[C/T]TGAGCTCAGGGGTTC | 54455 |
rs563535037 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250419 | ACACAGCAACAACTT[C/T]ATCTGAACCAGGATG | 54455 |
rs563541410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16298141 | TGAGGCAGTAGAATC[A/G]CTCGAACCCGGGAGG | 54455 |
rs563558535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16311135 | ATAAGCCGAGATCGC[A/G]CCCCTGCACTCCAGC | 54455 |
rs563569389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16330991 | CTGGGCATGGTGGCG[C/T]GTGCCTGTAGTCCCA | 54455 |
rs563583383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16336942 | GTAAGCAGAGATCAT[A/G]CCATTGCACTCTAGC | 54455 |
rs563640052 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16281808 | ATTACAGGCGCACAT[C/G]ACCACATTCAGCTGA | 54455 |
rs563641451 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16290471 | CTGAGGTGGGTGGAT[A/C]ACCTGAGGTCAGGAG | 54455 |
rs563658533 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16345187 | CCAGCACTTTGGGAG[A/C]CCAAGGCAGGCGGAT | 54455 |
rs563660459 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16352239 | TCTGCGGCCCGGGGA[-/G]GAGGAGAGGCCTCAC | 54455 |
rs563665629 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16351695 | TCCACAGTCACAGCA[C/T]GGATTGCTGTCTCAA | 54455 |
rs563728082 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16254223 | GATTATTTTTTTAAC[A/C]ATCTATTAACTGAAG | 54455 |
rs563751275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16303381 | TGCAGGATGCTGCAC[A/G]TCCCTGCCCCTTGCC | 54455 |
rs563776730 | in-del | -/C/CC | 0.00358779 | 0.0422022 | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16353256 | AAAACTAAGCCCCCA[-/C/CC]CCCCCCCCCCAACAC | 54455 |
rs563832827 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16260335 | TGTCTCAGCCTCCCA[A/G]GTAGCTGGGATTACA | 54455 |
rs563899964 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16352459 | CAGCTGCTGCTGCTC[A/C]GGCCGGGAGAAGACA | 54455 |
rs563919448 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16354312 | GGCGCCTGGCCTTTT[A/T]ATGTATTTATTGAGA | 54455 |
rs564004063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16297682 | CTGGCTAACACAGTG[A/G]AAACCCCATCTCTAC | 54455 |
rs564021891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16299965 | ACTATTTTAAGCACC[C/T]TAGCCTACTGAACTT | 54455 |
rs564103554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16346470 | GAGGCGGGCGGATCA[C/T]GAGGTCAGGAGATCG | 54455 |
rs564116025 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16353933 | CCACTTCAAGTTTCC[G/T]GTCTTTCTGCACCGA | 54455 |
rs564132154 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16305656 | GAGGTGGAGGCTGTA[G/T]TAAGCTGTGATTATG | 54455 |
rs564174549 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16272405 | GCTGGGATTACAGGC[A/G]TGCACCACCACGCCC | 54455 |
rs564200352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16307425 | AGGATCACCTGTGCC[C/T]AGGAGTTCAAGGCAG | 54455 |
rs564202346 | snp | A/G | 0.000164791 | 0.00907569 | missense, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16315324 | TCCAATACTGGGTGG[A/G]GCTCCTCATCTTGAT | 54455 |
rs564259879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16318829 | CTCGGGAGCAAAGAC[A/G]GCCACTCAGGGGAAT | 54455 |
rs564260935 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16267996 | TCAGCTAAAAATGAA[A/C]AATACAAAAGCCAGT | 54455 |
rs564289024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16314809 | GAATAACATGACCCC[A/G]GGAGGCAGAGCTTGC | 54455 |
rs564301928 | in-del | -/TG | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16279391 | ACTAGGACCTATGAC[-/TG]AGTCACTACACTCCA | 54455 |
rs564314304 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16246849 | AAACAGTTAAGACAA[G/T]TGTCCATTTTATTTG | 54455 |
rs564343289 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16339630 | TTATGTTCTTATGTA[A/G]ATTTTCTCAATAACC | 54455 |
rs564348604 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16291989 | GACTCTTTATTAAAC[A/C]ATTGTTTTTTATAAG | 54455 |
rs564365488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16277355 | AATCGAATAGTGACA[A/G]GCACATTAATACATC | 54455 |
rs564422068 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16312292 | ACTTGAGCCCGGGAG[A/T]CGGAGGTTGCAGTGA | 54455 |
rs564532583 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16335754 | CACCTGTAATCCCAG[A/C]TACTAAGGAGGCTGA | 54455 |
rs564533906 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16338951 | GAGTAGCTGGGATTA[C/T]AGGTGCACATCATCA | 54455 |
rs564569768 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16335196 | GACTCAGGAGTCTGA[A/C/G]GTGGGAGGACTGTTT | 54455 |
rs564588647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16263378 | GCGTGAACCCGCCAA[A/G]CTTGCATTGAGCCAA | 54455 |
rs564643097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16329546 | CCAAGATCGCACCAC[C/T]GCACTCCAGCCTGGG | 54455 |
rs564664753 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16333451 | ACCCCCCCCCCCCAT[A/T]TCCAAGAAGAAAAAA | 54455 |
rs564701485 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16340449 | CCTCAGCCTCCCGAG[G/T]AGCTGGAATTAAAGG | 54455 |
rs564773428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16320598 | AACCTCTGCCTCCCA[A/G]GTTCAAGTGATTCTC | 54455 |
rs564810196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16327244 | CAGTGTTGAAAGACT[C/T]CACTGAACCGTACTT | 54455 |
rs564814767 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | FBXO42 | GRCh38.p7 | 1:16275680 | CAAGAGTTCATCTCC[-/T]CAAGGGGGAATGAGA | 54455 |
rs564875451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16286040 | TATAGGTTCACACCA[C/T]GCCCAGCTAATTTTT | 54455 |
rs564888818 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FBXO42 | GRCh38.p7 | 1:16328980 | CAAGCCTGACCAACA[C/T]GGTGAAACCCCATCT | 54455 |
rs564907155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16294620 | ACAAAAAACAAAGAC[C/T]TACACAAGCATATTA | 54455 |
rs564926919 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16348644 | AGGTAGAGGTTACAG[A/T]GAGCAGAGATTGCGC | 54455 |
rs564964459 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16258647 | CAGGTGTAAGCCACT[C/G]TGCCTGTCCGTGTCA | 54455 |
rs565031614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16293914 | CTCATGTCCCCTCAC[C/T]CTTAGTCCAGTGCCC | 54455 |
rs565038782 | snp | C/G/T | 4.94877e-05 | 0.00497411 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251386 | GGGGGGCCAAAGAAA[C/G/T]TCCTATTTTCAGGTC | 54455 |
rs565076172 | snp | C/T | | | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16354425 | TTCTCGTGCCTCAAC[C/T]TCCTGAGTAGCTGGG | 54455 |
rs565087568 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16343855 | GTAGTGGTGCCCACC[A/T]GTAGTTCTAGCTACT | 54455 |
rs565105823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16263794 | AAACAAAAAACCCAC[A/G]GCCATACATTAACTT | 54455 |
rs565105964 | in-del | -/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16298423 | TTGAAATGAGCCAAC[-/T]TGGTACCAGGTTGGC | 54455 |
rs565131273 | in-del | -/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16269844 | TTTATGTTTTCTTTG[-/T]TTTTTTCTGTTTTGT | 54455 |
rs565143665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16350711 | GAGACTGTGCTACTG[C/T]ACTCCAGCCTGGATG | 54455 |
rs565187841 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16348282 | AGTTTTTGCAATATA[A/G]GCAACAACACGCTAA | 54455 |
rs565303907 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16302755 | CCTCAAGTGATCCGC[C/G]CTCCTCAGCCTCCCA | 54455 |
rs565315005 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16303018 | TGAGCTCAGGGGTTC[C/G]AGACCAGTCTGGACA | 54455 |
rs565369672 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16348461 | CCCAGCACTTTGGGA[A/G]GCAAAGGTGGGCGGA | 54455 |
rs565378814 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16296768 | TAATTCAGTTTAGCA[A/C]ACCAATATTTTTAAG | 54455 |
rs565395391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16344146 | GGAATTACAGGCATG[C/T]GCCACCACACCCAGC | 54455 |
rs565395842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16336609 | CAATCCACCTGCCTC[A/G]GCCTCCCAAAGTGCT | 54455 |
rs565455821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16316036 | TTAGCTGGGCATGGT[A/G]GCACATGCCTGTAAT | 54455 |
rs565460334 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16323300 | GTGGGCACCTGTAAT[C/G]CCAGCTACTCGGGAG | 54455 |
rs565477827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16303466 | TTTCTTACAGATTTC[C/T]GAATGTCAGAGGAGG | 54455 |
rs565503269 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16343976 | AAAAAACAACAACAA[A/C]AAAAGAAAACTGCAA | 54455 |
rs565538175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16309724 | AACACAAGGAGACCC[C/T]GTCTCGACAAAGTAT | 54455 |
rs565539565 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16280501 | TGGTTTATCATTATT[C/T]AATGGCAAAAACCGC | 54455 |
rs565563496 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16346140 | AGGAAACTTATTTGC[C/T]ACCACTGAGGTGACC | 54455 |
rs565571204 | in-del | -/TTT | 0.00318978 | 0.0398085 | intron-variant | FBXO42 | GRCh38.p7 | 1:16305998 | TGTGTCTATTACCTG[-/TTT]TTATCATTTTTATAC | 54455 |
rs565616301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16308949 | GGTTTCACCATGTTG[A/G]CCAAGCTGGTCTCAA | 54455 |
rs565632708 | snp | A/G | 3.31406e-05 | 0.00407053 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251155 | CTTCCAGACTCCGAC[A/G]CAGGGCACCTGGGGA | 54455 |
rs565667035 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16352037 | GAGGGGGTGGGTTCG[A/C]TCCCAACCCAAGGGC | 54455 |
rs565677798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16296483 | GGCAAAACCCCGTCT[C/T]TACTAAAAATAAAAA | 54455 |
rs565702590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16264973 | GCCACTTTCCCACAA[C/T]TGTAGTGTCTATTTA | 54455 |
rs565831510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16273524 | TACAAACAATGTTGA[C/T]GGCAGCTATATTCAA | 54455 |
rs565912588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16330420 | GCTGGGGTGGAAGGA[C/T]GGCTTGAGCCCAAGA | 54455 |
rs565942990 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16265678 | AAAAAAAAAGGCAAA[G/T]TCCATGTTCTGAGTA | 54455 |
rs565961183 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16338156 | CCCAGCTACTCGGGA[A/G]GCTGAGGCAGGAGAA | 54455 |
rs565973251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16337657 | GGAGGCCAAGGTGGG[C/T]GGATCACCTGAGGTC | 54455 |
rs565986077 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16282278 | TCCCCCAGGCTGGAG[C/T]GCAGTGGCGCGATCT | 54455 |
rs566023545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16285002 | AAAAATAAAGTTAGC[C/T]GGGCGTGGTGGCACG | 54455 |
rs566086549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16254060 | ACCTTTATAAAGATG[C/T]GCAGCAAAGTGTTAT | 54455 |
rs566146356 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16304440 | TGAATTTTATAATCG[A/T]CACTTGTCACATTCA | 54455 |
rs566148330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16260724 | TTTTTGAGATGAGGT[C/T]TCACTCTGGCACCCA | 54455 |
rs566153357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16283028 | TATCCCCAACTCCTG[A/G]GATTAGGTGAGTCTG | 54455 |
rs566280094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16289829 | TTCGCAGCTACTCAG[A/G]AGGCTAAGGCAGGAG | 54455 |
rs566284629 | snp | C/T | 1.76213e-05 | 0.00296822 | intron-variant | FBXO42 | GRCh38.p7 | 1:16253772 | AGGTAGTTAGGAGCT[C/T]CCAGGGACCATAATG | 54455 |
rs566368120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16291584 | ATGGGGTTTCGCTAT[A/G]TTGGCCAGGCTCGTC | 54455 |
rs566373099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16274290 | TGCTGCCTGGGTGAC[A/G]GAATGAAACTTTGTC | 54455 |
rs566378214 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16353262 | TAAGCCCCCACCCCC[C/G]CCCCAACACCAAACC | 54455 |
rs566382612 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16340032 | AATACAAAAAATTAG[C/G]CAGGCGTGGTGGCAG | 54455 |
rs566413631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16281392 | CCTCTCAAGGTCCAC[A/G]TACATCTCCTGGGAC | 54455 |
rs566426190 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FBXO42 | GRCh38.p7 | 1:16333084 | GACAAATTCCTACTC[C/T]GCCACGTAAGAGTTA | 54455 |
rs566486656 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16328774 | GCTCCTTGGTGAAAC[A/G]GCAGAATCTAGGAGG | 54455 |
rs566498111 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16267755 | GGATCTCAGGATTCA[A/G]GGTATACATTATTAT | 54455 |
rs566507292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16300300 | AATGGGCTTAGTTTA[C/T]GACACATACTAATCA | 54455 |
rs566509307 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16307517 | CCCTGTCTCTTAAAA[A/C]ACAAGCAAAAAAAAA | 54455 |
rs566539706 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16325164 | GATCTCTTGAGCCCG[A/C]GAGGTGGAGGCTGCA | 54455 |
rs566587164 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16326303 | TCAGGTGATCCATCT[A/G]CCTGGGCCTCCCAAA | 54455 |
rs566596324 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16261713 | ATATCAATTTTTTTT[G/T]TTTGTTTTTGAGACG | 54455 |
rs566629311 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16346644 | AGTGAGCCGAGATTG[A/C]GCCACTGCACTCCAG | 54455 |
rs566646066 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16346168 | ACCACTTCACCAATT[A/C]TTTACGAAGAAATTT | 54455 |
rs566648782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16305197 | GAAGACAAGCCTGGG[C/T]AATACAGTGAGACCC | 54455 |
rs566652857 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16267912 | ACTAAAGGAAATTCT[C/G]TATTGGCATTGTTTT | 54455 |
rs566673493 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16295931 | CATGCTGGTTGGAGC[C/T]GACTAGAAAACAGAA | 54455 |
rs566697421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16269984 | CATCAGCCTTCCAAG[C/T]AGATGGGACCACAGA | 54455 |
rs566735403 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16276677 | AAGGATAAGGCATCA[A/T]ATGAAATGAAATTTA | 54455 |
rs566792846 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16306805 | CCAGGCTCAAGCAAT[A/T]CTCCTACCTCTGCCT | 54455 |
rs566820440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16340983 | CAGCAGTAAAGCATT[A/G]TTTACTAATGTCCAT | 54455 |
rs566860724 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16348326 | CAACTACAGCACTAA[G/T]GTAAATAACTTGTAC | 54455 |
rs566876896 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16341735 | CAGCGCTTTGGTAGG[C/T]CAAGGCGGGCGGATC | 54455 |
rs566941200 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16321002 | ATGAATCAATGGAGG[A/C]TGCAAAAGTTTATTT | 54455 |
rs566996799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16292488 | TTTTGTAGAGATGGG[A/G]GTCTCACCATGTTGC | 54455 |
rs567037011 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16262816 | TCAAGCTCAGGTGAT[C/T]CTCACACCTCAGCCT | 54455 |
rs567046088 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | FBXO42 | GRCh38.p7 | 1:16313358 | AGAAAGAAAGAAAGA[A/G]AGAAAGAAAGAAAGA | 54455 |
rs567057260 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16314041 | TCACTGCAACCTCTG[A/C]CTCCTGGGTTCAAGC | 54455 |
rs567092032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16306576 | AGCCTTATGAAAGAG[C/T]ATGATAAAACAATGT | 54455 |
rs567097136 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16327356 | ATTTTTCTTCACTGA[C/T]GAATTAACTGAAATA | 54455 |
rs567126148 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16264133 | ATTTTTATATGGAGT[A/G]GCCGTAGATAAAATG | 54455 |
rs567231868 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16257494 | AAATTCTGAAAAAAA[A/C]CACTTTGGCTTATGC | 54455 |
rs567234757 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16344338 | ATTTTTTTTTTTTTT[C/T]TTGAGACAGAGACTC | 54455 |
rs567238327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16329095 | TTGAACCCAGGAGGC[A/G]GAGGTTGCAGTGAGC | 54455 |
rs567254371 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16308485 | GGAAACACAGTGAGA[C/T]CCATCTCTCTTTTTT | 54455 |
rs567282080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16271845 | TCATTGGATGCTCAA[C/T]AGTCCTCTGTAGGCT | 54455 |
rs567358791 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16316128 | GAGCCGAGATCATGC[C/G]ACTGCACTCCAGCCT | 54455 |
rs567384965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16334474 | AAGACTAATGACCTG[A/G]GAACACCTCCCTGGC | 54455 |
rs567405775 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16335380 | TGGGTTCAAGTGATC[A/C]TCCTGTATTGGCATC | 54455 |
rs567416727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16273533 | TGTTGATGGCAGCTA[C/T]ATTCAAAGTAGAAAC | 54455 |
rs567429531 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | FBXO42 | GRCh38.p7 | 1:16252509 | CTGGTCTTGAAAGGA[-/T]TGTGGACTCTTCAGA | 54455 |
rs567483922 | snp | A/C | | | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16353847 | GCCACCGCACCAGGC[A/C]TATTGATAATAACTA | 54455 |
rs567522499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16349952 | TGAGATAGCTTCTCC[C/T]TGGGACCTCAGTGTT | 54455 |
rs567543436 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16347111 | ACATTTATCAGATTT[A/G]TATAGTGTACATATA | 54455 |
rs567561594 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16270932 | GACATATGGTGATAA[A/G]TGCCAAGGGGGGAAA | 54455 |
rs567570321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16279500 | GCATCCTGCTCCTCA[C/T]CAAAAAAATTTTAAA | 54455 |
rs567586839 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16286109 | ACCCTTAGGCTGAAG[C/G]AATTCTGCCTCAGCC | 54455 |
rs567599688 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16277950 | GGGAGGCTGAGGCAG[C/G]AGGATCACTTGAGCC | 54455 |
rs567662067 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16330594 | CAGGCAGATCACAAG[G/T]TCAACAGATTGAGAC | 54455 |
rs567688381 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16336672 | GGGCCAAGGTTTAAT[G/T]TGGACATATTCATAG | 54455 |
rs567727687 | in-del | -/T | 0.0588605 | 0.161139 | intron-variant | FBXO42 | GRCh38.p7 | 1:16296948 | ACCCCCCGCTTTTTG[-/T]TTTTTTTTGAGACAG | 54455 |
rs567734436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16323967 | TGTCATTATGAACTC[A/G]TAAAGTGAACCACTT | 54455 |
rs567820735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16287254 | TTGAAACATTCGTTT[C/T]TCAGATACCCACATG | 54455 |
rs567841501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16302402 | TAACTGACTCACAGT[C/T]CCACATGGCTGGAGA | 54455 |
rs567922630 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16337696 | AAGACCAGCCTGCCC[A/G]ACATGGTGAAACCCC | 54455 |
rs567972868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16343892 | GCTGAGGCAGGAGGA[C/T]CGCTTGAGCCAGGAG | 54455 |
rs568002121 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16295314 | CTCTGTCCTCCCATT[C/G]CTTTCCTCCAATTCT | 54455 |
rs568014882 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16255610 | AAAATGCTGGGATTA[C/G]AGGTGTGAATTAGGC | 54455 |
rs568020179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16345412 | TGGGTGATGGAGCGA[A/G]ACTCTGTCTTAAAAA | 54455 |
rs568087147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16292668 | AGGGAGAAATAAGCA[C/T]AGTAGTTGGCAGAGG | 54455 |
rs568096626 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | FBXO42 | GRCh38.p7 | 1:16251951 | GCTAGAAGTCAGACA[G/T]GGGAACAATCGCTGC | 54455 |
rs568109269 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16344755 | AAGAAAAAATCCCAT[A/C]AATGTGTTAAATTCA | 54455 |
rs568135749 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16259038 | ACCCACCTCACCCAG[C/T]CAGAAATCTTCTCTA | 54455 |
rs568183025 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16346327 | TCTAAGGGAACATTA[A/C]CAGCTAAAACCAAAA | 54455 |
rs568387933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16310544 | CCCTCCCCAAAATAA[C/T]TGATAAGCCAGAATT | 54455 |
rs568404344 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16312075 | TGAAAAGAAATGGAG[A/G]AAGCCGGGCACGGTG | 54455 |
rs568416707 | snp | G/T | 0.135484 | 0.22223 | intron-variant | FBXO42 | GRCh38.p7 | 1:16261717 | CAATTTTTTTTTTTT[G/T]TTTTTGAGACGCGTC | 54455 |
rs568423133 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16353322 | CAGTCTAAAATGTAA[A/C]CAACCTGAGAGACTG | 54455 |
rs568428569 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16354157 | CGTGCCCAGCTAATT[C/T]TTGTATTTTCAGTAG | 54455 |
rs568438797 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16337178 | CAATGCTTCTCAAAT[C/T]TTAATGTGAATCTAG | 54455 |
rs568458206 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16259137 | TTAAAGAGGCTGTTG[A/T]CTTTCATATAGCCTT | 54455 |
rs568472285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16268259 | GAGCCAAACTGAAAT[A/G]TGGTAAAATCTTACT | 54455 |
rs568499587 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16308994 | GTGATCCGCCCACCT[C/T]GGCCTCCCAAAATGC | 54455 |
rs568525133 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16298793 | GAGATTATAGGCGTG[A/C]GCCACCGCGCCCGGC | 54455 |
rs568527621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16253998 | ACTTTATCTCTAAAA[C/T]GAAAATACTGTTACT | 54455 |
rs568586668 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16305360 | ACCACCATATCACAG[A/C]CTGGGTGACAGAGTG | 54455 |
rs568656171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16275652 | GGAAGAATAAAAATA[A/G]AAAGCCATAGTTCAA | 54455 |
rs568658628 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16252866 | GGAATGGGAAGAATA[C/T]AGATATGAATATTCA | 54455 |
rs568674012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16331830 | CTGAGGCGCGCAGAT[C/T]ACCTGAGGTCAGGAG | 54455 |
rs568715072 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16346720 | AACAAGAGAAAATAA[A/G]TTACTAAGCTAAATT | 54455 |
rs568727567 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16276953 | GAAAGAATAGAAAAG[A/T]CTCATGAGTTTGACC | 54455 |
rs568755251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16327437 | TACTGTCAGAAGCCT[A/G]GCTGAAAAACCAAAA | 54455 |
rs568793899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16333653 | GCTATGGCTTCCAAT[A/G]AAGTCAAGACAAGGC | 54455 |
rs568803390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16274917 | CTTAATAGAATAATA[C/T]TGTTTTTAAAAAAAG | 54455 |
rs568833399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16340748 | ATAGGCTTAAAATAC[A/G]GTTAATAAAACTTGC | 54455 |
rs568979714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16321138 | TACTGCTGTAATAGC[C/T]AATGTCAAGCAATTT | 54455 |
rs568982465 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16322992 | TGCCTTTGGTTTCTA[C/T]TCAACTAGACATCTG | 54455 |
rs569002328 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16286235 | CATAGCTTTAAATCC[A/G]TCTGGATTAGTCTAT | 54455 |
rs569005851 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16254428 | ACAATGACTAATGAA[A/C]GCTGCAGTTTTATCA | 54455 |
rs569071317 | in-del | -/C | 0.00318978 | 0.0398085 | intron-variant | FBXO42 | GRCh38.p7 | 1:16303652 | GACTCACTGCAACCT[-/C]CGCCTCCCGGGTTCA | 54455 |
rs569081497 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16263491 | ACACGGCCGGCCAGG[C/T]GTGGTGGATCACCTG | 54455 |
rs569092519 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16299658 | ATTATTATTATTATT[A/T]TTTTGAGATGGAGTC | 54455 |
rs569130895 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FBXO42 | GRCh38.p7 | 1:16306301 | AGATTACAGGCATGA[A/G]CCACCGCGCCCAGCC | 54455 |
rs569192113 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16248698 | AAGGACCCCACATGA[C/T]CGAACAGTCTTTGCC | 54455 |
rs569255599 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16301618 | CAGTGAGCCAAGACC[A/G]CGCCACTGCACTCCA | 54455 |
rs569271336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16335446 | CCCCCGGCTCATATC[A/G]CTTCCTAACTAATCT | 54455 |
rs569280326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16348826 | GACAGTACTAATAAC[C/T]ACCTATAATCAACAT | 54455 |
rs569282148 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16257134 | AACAAATGAGCACCC[A/C]TTCCCATCCCTTTAA | 54455 |
rs569317404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16341769 | TGAGGTCAGGAGTTC[A/G]AGACCAACCTGACCA | 54455 |
rs569394381 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16333121 | CTTGAGGTTCTATCC[C/T]CTCCAGCCAATTAAG | 54455 |
rs569413503 | in-del | -/AAG | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16317934 | GAAGAAAAAAAAAAA[-/AAG]AAGAAGAAGAATATA | 54455 |
rs569455788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16314961 | TAAAAACAATCCTCA[C/T]TTTAAAATGCAAATG | 54455 |
rs569471251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | FBXO42 | GRCh38.p7 | 1:16316507 | TTGGGATTCTGAGGC[C/T]GGCAGATCACCTTAG | 54455 |
rs569494658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16307643 | AGCATACAACAATGA[A/G]CAAGTAGAATTTGAA | 54455 |
rs569520658 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FBXO42 | GRCh38.p7 | 1:16286928 | CCACCCAGTTCTTAC[C/T]TTTTGTGAATACTTT | 54455 |
rs569622390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16258250 | AGGACTGTCTTTCTT[A/G]TGATCTCACTTAGGG | 54455 |
rs569624457 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16265582 | TCATTTTACAGATGA[A/C]TAATGGTAGGTGAAG | 54455 |
rs569625377 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16315751 | GATCTGACTGACCGA[C/T]AGCAAAGGGAAGAGC | 54455 |
rs569694410 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16302991 | CAAACCATATCTGGC[A/G]GGCACACTGCTTGAG | 54455 |
rs569711112 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16346637 | AGCTTGCAGTGAGCC[A/G]AGATTGCGCCACTGC | 54455 |
rs569719503 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16271892 | ACTTGTAATCTCAGC[C/T]CTCTGGGAGGCTGAG | 54455 |
rs569782553 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16258909 | TATCCAGCTAATTTT[A/T]AAAATTTTTTTGTTG | 54455 |
rs569784731 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FBXO42 | GRCh38.p7 | 1:16329179 | AAAAAAAAAAAAAAA[A/G]AAAGAAAATTGATGG | 54455 |
rs569785599 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16351016 | ATTTAACACAGCATC[A/G]CTAATGGCCATAAGA | 54455 |
rs569795725 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16266457 | TAACCACTCTGTGCA[A/G]ACTCGCTTTCTCAGA | 54455 |
rs569802009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16279253 | GGAAGATATTGTTCT[C/T]TTAGAGAATAGCCCT | 54455 |
rs569824235 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16334205 | TTGGGAGGCCAAGGC[A/G]GGCAGATCATGAGGT | 54455 |
rs569844083 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16288680 | TAAGAAGTCTTGGCC[A/G]GGCGCAGTGGCTCAT | 54455 |
rs569865791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16335864 | AGTGCGAGACTCCAT[C/T]GCGCCAAAAAAAAAA | 54455 |
rs569871370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16344607 | TCCCAAAGTGCTGGG[A/G]TTACAGGCGTGAGCC | 54455 |
rs569906811 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16252145 | GTGAGAAATGCCAAA[A/G]GAGCTATGGCTAATG | 54455 |
rs569911103 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16272478 | TAGTCAGGCTGGTTT[C/T]GAACTCCTGACCTCA | 54455 |
rs569911953 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16289941 | CTCTCCCCTTATTCT[A/G]TACTTCATTCCGTTT | 54455 |
rs569979517 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | FBXO42 | GRCh38.p7 | 1:16343964 | TGGCAAAAAAAAAAA[A/C]AACAACAACAAAAAA | 54455 |
rs569979834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16323570 | GGGAGGCTGAGGTGC[A/G]CGGATCTTTTGAGGT | 54455 |
rs570001930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16274219 | GCTGAGGCAGGAGGA[C/T]TGCTTGAGCCCAAGA | 54455 |
rs570023621 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16257741 | GCTGGAGTGCAATGA[C/T]GCAATCTCGGCTCAC | 54455 |
rs570029628 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16324057 | AGAGATTTAAAGAAG[A/T]TCATAAAGTGATTCA | 54455 |
rs570033002 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16274812 | GGCCAGGATTCTCTC[A/G]ATCTCCTGATCTCGT | 54455 |
rs570127599 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16290234 | GATTTCACTGGGAAA[G/T]TACATTAATTCCAAC | 54455 |
rs570138792 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FBXO42 | GRCh38.p7 | 1:16310925 | GTTGCAGTGAGCCAA[C/T]ATTGTGCCACTGCAC | 54455 |
rs570138800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16318177 | TAATCCCAGAACTTT[A/G]GGAGGCCTAGGCGGG | 54455 |
rs570172453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16317722 | TGAGGTCAGGAATTT[A/G]AGACCAGCCTGGGCA | 54455 |
rs570185860 | in-del | -/AATAAT | 0.00304413 | 0.0388947 | intron-variant | FBXO42 | GRCh38.p7 | 1:16331423 | CTGTCTCAAAAAGAA[-/AATAAT]AATAATAATAATAAT | 54455 |
rs570202594 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16282917 | ACCCAGGAGGCAGAG[G/T]ATGCAGTGAGCTGAG | 54455 |
rs570222968 | in-del | -/AAAAAAAAAAA | 0.434543 | 0.168653 | intron-variant | FBXO42 | GRCh38.p7 | 1:16341610 | GAGACTGCGTCTTTT[-/AAAAAAAAAAA]AAAAAAAAAAAAAAG | 54455 |
rs570239776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16290917 | GAGCTGACTAAGACA[C/T]CAACCAATAGGAGAA | 54455 |
rs570242735 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16280740 | ACATCCGCCACTGCA[A/C]TCCAGCTTGGGAGAG | 54455 |
rs570255704 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16302756 | CTCAAGTGATCCGCC[A/C]TCCTCAGCCTCCCAA | 54455 |
rs570269459 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16330708 | GCACTTTGGGAGACC[A/G]AGGAGGTGAATCACC | 54455 |
rs570285959 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | FBXO42 | GRCh38.p7 | 1:16296426 | GGAGGCTGAGGCAGG[C/G]GGATCATGAGGTCAG | 54455 |
rs570376162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16298533 | TTTATTTTCTGAGAT[A/G]GAGTCTCACTCTGTC | 54455 |
rs570390490 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16288032 | GCGCCTGTAATCTCA[C/G]CTACTTGGGAGGCTG | 54455 |
rs570418519 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16339294 | ACACAATGTCACACT[A/C]TTTCATATTGTTATA | 54455 |
rs570496906 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | FBXO42 | GRCh38.p7 | 1:16313871 | CACTTAAGATGCAAT[A/G]AAGCCACTAACTGCT | 54455 |
rs570522255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16264768 | AACTGAATAATCAGA[C/T]AGACACCCTATACAA | 54455 |
rs570545080 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16269034 | CAGGCTGGTCTCGAA[C/T]TCCTGACCTCGTGAT | 54455 |
rs570577615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16332425 | AAAAGATTTAATAAA[C/T]GACATTGCTATATTG | 54455 |
rs570583432 | in-del | -/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16277959 | AGGCAGGAGGATCAC[-/T]TGAGCCCAAGAGGTC | 54455 |
rs570598250 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16267332 | TACAAAGTTACAGAA[A/C]CTCTAAACTCCTGCT | 54455 |
rs570602321 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | FBXO42 | GRCh38.p7 | 1:16352273 | GCCCAGCCCGCTCCA[C/T]GCTCTCGGGTTCGCT | 54455 |
rs570608338 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16352639 | TCGGGGGAGCTAGGC[C/G]TCCGCACCCGCCTTC | 54455 |
rs570624784 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16353217 | TAAACTCTGTAAGCC[A/G]AAAAAACAAAACAAA | 54455 |
rs570645813 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16311554 | TATAAAATAAAAAAT[C/G]GGTCAAAGACCTGAA | 54455 |
rs570687678 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16297963 | GGGCACAGTGGCTCA[A/T]GCCTGTAATCCCAGC | 54455 |
rs570705500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16345513 | CTGTAGCAATGAGCA[C/T]CCCTAGCACACAGAT | 54455 |
rs570717732 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16326086 | TTGAGATGGAATTTC[A/G]CTCTTGTTGCCCAGG | 54455 |
rs570774751 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16313132 | CAATTTTGCTGTGAA[A/C]CTAAAAGTGCTCTTT | 54455 |
rs570775053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16304325 | GGTTTCACCATGTTG[A/G]CCAGGCTGGTCTCAA | 54455 |
rs570781491 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16336878 | TAATTCTAGCTACTT[C/G]GGAGGCTGAGGCAGG | 54455 |
rs570809863 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16346740 | TAAGCTAAATTACTG[G/T]ACTGAACAGTACATT | 54455 |
rs570814696 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16254641 | CCATAACTGTTTTAA[A/T]ATATGAAGATGGAAA | 54455 |
rs570818900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16300224 | TACAGTATGAATACT[A/G]GGCTAACAAATAATA | 54455 |
rs570850642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16285078 | TTGAACCTAGTTGGC[A/G]GAGGCTGCAGTGAGC | 54455 |
rs570879371 | in-del | -/TTTGTTTG | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16308676 | GCTAATTTCTGTTTT[-/TTTGTTTG]TTTGTTTCATAGAGA | 54455 |
rs570921240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16276136 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGCCGAGG | 54455 |
rs570971460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16255495 | GTGTGCCACCATGCC[C/T]GGCTAATTTTTGTAT | 54455 |
rs570989220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16268387 | AAAAGCATGTATTCT[A/G]GAAAAATCCCAGGGT | 54455 |
rs571014079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16319163 | TTGGCGGGGGGTGGG[A/G]AAGGAAACGAAGAGT | 54455 |
rs571025997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16275819 | TTGGAGACCAGCCTG[A/G]CCAACATGGCAAAAC | 54455 |
rs571148698 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16321576 | ACTGGAATCTGAACT[C/G]CCTGGAGGCAGGACC | 54455 |
rs571149752 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16340814 | TTATAGAACAACTGA[A/C]CCCTTATTTCACAAA | 54455 |
rs571186346 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16328468 | CAGATGGCTAGACCA[A/C]ATTTTCTTATTGGAG | 54455 |
rs571193679 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | FBXO42 | GRCh38.p7 | 1:16311249 | AGCAGGCCCAGGTGG[-/T]TAAGATTGCTTGAGC | 54455 |
rs571224177 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16334429 | GCCTCAAAAAAAAAA[A/C]AAAAAAAAAAACAGA | 54455 |
rs571231052 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16263580 | TACAAAAAATTAGCC[A/C]GGCATGGTGGTGCAC | 54455 |
rs571263996 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16277908 | TTAGCTGGGCTTGGT[A/G]GCATATGTCTATAGT | 54455 |
rs571310010 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16295858 | CTAGTCCCAAAGCAA[A/C]AGATTGAAAAAGCAT | 54455 |
rs571322631 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16322054 | AGGCGCCTGTAATCC[C/T]AGCTACCTGGGACAT | 54455 |
rs571329614 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16315567 | CTTCAGCACTTTCCA[A/C]TACCACTTGTGAGCC | 54455 |
rs571329893 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16307881 | TTGATCAACAGATTC[A/C]ATGCAATCCTAGTCA | 54455 |
rs571331359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16286271 | CAGTGCTATGAAGAA[A/G]TACCCAAGACTGAGT | 54455 |
rs571337320 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16249725 | TGATTTCTGTAGGCA[C/T]CTGAGCTTTGTAAAA | 54455 |
rs571370875 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16347471 | GTGAGCCAAGATGGC[A/G]CCACTGCCCTCCAGC | 54455 |
rs571373706 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16263905 | AACTTCCACCTCCCA[A/G]GTTCAAGCGATTCTC | 54455 |
rs571379756 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | FBXO42 | GRCh38.p7 | 1:16246709 | GGGTTTCACTATGTT[G/T]GCCAGGCTGGTATCA | 54455 |
rs571406287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16279326 | AGCTTGAAAGAAGGG[A/G]GGCTGAGGCAGGATG | 54455 |
rs571465535 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16328983 | GCCTGACCAACATGG[C/T]GAAACCCCATCTCTA | 54455 |
rs571537391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16327703 | TTTTAAGATGGGAAA[A/G]TTTTTGTTTTGTTTT | 54455 |
rs571546649 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16322086 | TAAAAAAAATTACAT[C/T]ATTAGTATATCCAGA | 54455 |
rs571554864 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16285440 | CACCATGCCCAGCTA[A/C]TTTTTGTATTTTTAG | 54455 |
rs571561807 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16292402 | CTCAAGCAATCCTCC[C/T]GTCTCACCCTCCCAA | 54455 |
rs571610929 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16324306 | ATTATGCTTAGATCC[C/T]ACACAGGGTACAAAA | 54455 |
rs571626315 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16248720 | GTCTTTGCCAAGCAA[A/G]GATTGGCAACAGCAC | 54455 |
rs571628109 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16295097 | TACCCTTTAAAACAA[C/G]GTCCAGAGGAAAGCT | 54455 |
rs571654799 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16343027 | TAGCCTGTAGAACCA[G/T]GAGCTAAATAAACCT | 54455 |
rs571661108 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16269430 | CTCTGTTCCCCAGGC[C/T]GGAGTGCAGTGGCAC | 54455 |
rs571709094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16335551 | GTAGTATTAAACTTC[A/G]TGATGCAAATCTGGA | 54455 |
rs571734217 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | FBXO42 | GRCh38.p7 | 1:16349071 | GGATTTTTGAGAATG[A/C]AGAAGCCATAACTGG | 54455 |
rs571782585 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | FBXO42 | GRCh38.p7 | 1:16336871 | ACGCCCGTAATTCTA[C/G]CTACTTGGGAGGCTG | 54455 |
rs571783673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16329947 | GAGCAAGATACCATC[C/T]CAGGGCGGGGGAAAC | 54455 |
rs571786089 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16282414 | TATTTTTAGCAGAGA[C/T]GGGGTTTTGCCACGT | 54455 |
rs571799527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16294205 | AAAACCATTGTTTTT[A/G]TTTTTTCCCCCAGGA | 54455 |
rs571861868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16302292 | TCAACGCCTGTAATC[C/T]AGGCACTTAGCAAGA | 54455 |
rs571882508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16349870 | CTCAAAAAACAAACA[A/G]AAAGAGTTAATTCAT | 54455 |
rs571902511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16308604 | TCCTGAGCACAAGGG[A/G]TCCTTCCACCTCAGC | 54455 |
rs571915056 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16310022 | AACACAGTGAAACCC[C/T]GTCTCTACTAAAAAT | 54455 |
rs571937358 | in-del | -/CG | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16333446 | TGAGACCCCCCCCCC[-/CG]CCATTTCCAAGAAGA | 54455 |
rs571943198 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16280547 | AACCTAATAATTGTC[A/C]CAGTGTGCTATACTA | 54455 |
rs571974131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16302519 | AACTGCCACCTTTTT[C/T]TCTTTTTTGAAACGG | 54455 |
rs571984916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16295541 | GATTACAGGTGTGCA[C/T]CACCACACCCAGCTA | 54455 |
rs572000809 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | FBXO42 | GRCh38.p7 | 1:16334820 | GGCAAACAGGTATGC[-/A]AAAACATTCAAAGTT | 54455 |
rs572007004 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16288213 | GAGGCAGACGGATCA[C/T]GAGGTCAAGAGATCG | 54455 |
rs572007741 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16343444 | CCAGCTACTCAGGAG[C/G]CTGAGATGGGACAGT | 54455 |
rs572010708 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16309269 | TTTTTAGTAGAGATG[G/T]GGTTTCACCACGTTG | 54455 |
rs572012906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16301955 | TGGCACAAACAGAAT[C/T]TGTCATATCCATTTT | 54455 |
rs572013355 | in-del | -/GT | 0.307423 | 0.243316 | intron-variant | FBXO42 | GRCh38.p7 | 1:16271259 | TGCGTGTGTGTGTTG[-/GT]GTGTGTGTGTGTGTG | 54455 |
rs572084023 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | FBXO42 | GRCh38.p7 | 1:16352369 | CGACAGCCGTGCTCG[C/G]GGCTCCTCACAGCTG | 54455 |
rs572113156 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250218 | GCACCTGAAGCATGA[C/G]AGTCTAAAACCCTCC | 54455 |
rs572131097 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16279880 | GAGACAGAGTCTTGC[G/T]TTGTTGCCCAGGCTG | 54455 |
rs572146885 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16351542 | AATCTTAACAAACCG[A/T]AGGTTTCAAACGAAC | 54455 |
rs572191716 | snp | C/T | 0.000149605 | 0.00864754 | intron-variant | FBXO42 | GRCh38.p7 | 1:16252427 | AGAAAAAACCAATAA[C/T]AAGACTCAGGTGTGA | 54455 |
rs572215325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16264461 | AAAATAACAAAGCCA[C/T]TGGGCTTCTAAATTC | 54455 |
rs572234021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16342532 | ATGCTGGAGTAAACC[A/G]TGATCGCCCACTGCA | 54455 |
rs572237478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16315881 | GGGTTAAGAAATAAC[C/T]GTTTTTCGACCAGGC | 54455 |
rs572241590 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16257730 | TTGTCACCCAGGCTG[A/G]AGTGCAATGATGCAA | 54455 |
rs572320069 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16260062 | AACAGTGTGCCTATG[C/G]TTGGGGATTACGGGA | 54455 |
rs572348825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16258499 | ATAGCTAGGAATACA[A/G]GCAAGCACCACCATG | 54455 |
rs572360168 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16266688 | GATGGATTTTGCTGA[A/T]AAAACCAAAGCTGGG | 54455 |
rs572411827 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16259204 | GATCTATCTCCTAGC[C/G]CAATTAGAAAGCCTA | 54455 |
rs572420862 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | FBXO42 | GRCh38.p7 | 1:16301681 | ATCTCAAAAAAAAAA[A/C]AACAACAAAAAAAAA | 54455 |
rs572430083 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16248906 | CCTACGAAGACCACA[C/T]CATAAAAGCTAATGG | 54455 |
rs572464295 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16303285 | GCTAGTTGCATGTTT[C/T]AGACTTGCAGTATTT | 54455 |
rs572483700 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16279027 | GTGATCTGCCTGGGT[C/T]GGCCTCCCAAAGTGC | 54455 |
rs572502211 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16310142 | GAGCTTGCAGTGAGC[C/T]GAGATCACACCACTG | 54455 |
rs572638228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16275855 | CTCTACTAAAAAAAT[C/T]AGCCAGGCGTGGTGG | 54455 |
rs572696769 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16266120 | ACTTTTGAAAGAAAA[A/C]GTCAGAACCCTTTCT | 54455 |
rs572793952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16318557 | AAGCATACACATAGA[A/G]GCAGGCATCTCATTT | 54455 |
rs572835774 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16293638 | GTATCCACTCAGTAG[C/G]CTCCTCCTATATTTG | 54455 |
rs572848661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16281603 | ACTCTTGAGTAGCTT[A/G]GACTACAGGTATGGA | 54455 |
rs572851813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16268574 | AAGGTTAACCAGGAA[C/T]AGGTCCATGGGTCAG | 54455 |
rs572861196 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16333291 | TCATAAGTTACAATT[G/T]TGCTTATTAACCACT | 54455 |
rs572894247 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16261501 | CACAAAGTAGGAGCA[A/T]CTTAAATAGCTCAAC | 54455 |
rs572902618 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16312098 | GCACGGTGGCTCACA[C/G]CTGTAATCCCAGCAT | 54455 |
rs572911476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16325213 | ACTGCACTCCAGCTT[A/G]GGCAACAGAGCAAGA | 54455 |
rs573003959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16345607 | GTAATCCCAGCACTT[C/T]GGGAGGCCGAGGCAG | 54455 |
rs573023002 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16262425 | TTTATGGTGAGATCA[C/T]ATGGGGTGTGGTGGC | 54455 |
rs573025546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16327018 | TCTCTCTCTATGACC[C/T]ACTTCTAAATGTCAT | 54455 |
rs573042619 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FBXO42 | GRCh38.p7 | 1:16337839 | CAGTGAGTGGAGATC[A/G]CGCCACTGTACTCCA | 54455 |
rs573094949 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16305587 | GGTGTGATGGGGCAC[G/T]CCTGTAGTCCTCATA | 54455 |
rs573122558 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16301807 | ACAGCTTAAAATATA[C/T]ACATATATTTTAATT | 54455 |
rs573133020 | in-del | -/GCCTTA | 0.0209421 | 0.100162 | intron-variant | FBXO42 | GRCh38.p7 | 1:16257792 | TCAAGTGATTTTCCT[-/GCCTTA]GCCTTAGCCTCCTGA | 54455 |
rs573197867 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16331998 | AGGTTGTGTTGAGCC[A/G]AGATCGTGCCATTGC | 54455 |
rs573204519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16306136 | AAGTGATTCTCCTGC[C/T]TCAGCCTCCCGAGTA | 54455 |
rs573206713 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16299094 | CTTGGCTCACTGCAA[C/T]CTCTGCCTCCTAGGT | 54455 |
rs573271887 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16269689 | AGCCACCATGTCCAG[C/G]TAATTTTGTATTTTT | 54455 |
rs573311848 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16333988 | GTAAAAATAATAATC[C/G]ATCAGAAACTTCAAA | 54455 |
rs573343853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16347897 | GGGAGGCTGAGGCAG[A/G]AGAATGGCGTGAACC | 54455 |
rs573444402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16254139 | GAAGTCATCCTGAGA[C/T]CCTCCCTCTGCTCTT | 54455 |
rs573452862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16291260 | ATTCAGAAGGACTAA[C/T]TGACATTTCAGTTAG | 54455 |
rs573461220 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16303873 | GCTTCAGCCTCCCCA[C/G]TAGCTGCGACTACAG | 54455 |
rs573467170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16339818 | CACCTGGCCAAGCAC[A/G]GTGGCTCACACCTGT | 54455 |
rs573544880 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16314844 | AGCCGAGATTGCGCC[A/T]CTGCACTCCAGCCTG | 54455 |
rs573555634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16256837 | TATCCATAGATCACC[C/T]TTCCCTGGAAGAGCA | 54455 |
rs573564419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16307969 | GAAGCACAAGACCCA[A/G]AATAGCCAAGAAAAC | 54455 |
rs573583870 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16283736 | TCCTGACCTAGTGAT[A/C]CACCTGCCTTGGCCT | 54455 |
rs573646798 | in-del | -/G | | | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250368 | TTGGTCTAGTTACCA[-/G]GCAAGGTAGAAAAAG | 54455 |
rs573660453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16300810 | TCAGGAGACCCCCTA[C/T]ATCAATCTGAAAAGG | 54455 |
rs573682403 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16341700 | TCTGGGCCGGGTGCG[A/G]TGGCTCATGCCTGTA | 54455 |
rs573735763 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16293731 | ATAAACAGGTTTAAG[A/T]CCCTGGCCTAGACAT | 54455 |
rs573791633 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16265190 | CCTCTGCCTCCCAGT[G/T]TCAACGGATTCTCCT | 54455 |
rs573798378 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16345667 | ATCCTGGCTAACAAG[A/G]TGAAACCCTGTCTCT | 54455 |
rs573815294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16320268 | CGGGAGGCTGAGGCA[A/G]GAGAATCACTTGAAC | 54455 |
rs573829938 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16316670 | AACCTGGGAGACAGA[G/T]GTTGCAGTGAGTCGA | 54455 |
rs573830373 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16272727 | GCAAGTAGGATACTT[C/T]GGGTAAAAGGACATG | 54455 |
rs573847888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16263017 | CTTTGGTAATTTCTA[C/T]ATCAAAGAATAACAT | 54455 |
rs573946309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16315936 | AGCACTTTGGGAGAC[C/T]GAGGCGGGCAGATCA | 54455 |
rs573954656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16307238 | GCGCAGTGGCTCACA[C/T]CTGTAATCCCAGTGC | 54455 |
rs574014644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16270273 | AGACCCCACCTCTCA[A/G]TACTGCTACACTGGG | 54455 |
rs574047881 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | FBXO42 | GRCh38.p7 | 1:16257897 | TGTTGGCCAGGCTGG[C/T]CTCAAACTCCTGACC | 54455 |
rs574048252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16309366 | ATAGGCATGAGCCAC[C/T]GCGCCTGGCCAACCC | 54455 |
rs574081524 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16323203 | GCGGAGGAATCACAA[C/G]GTCAGGAGTTTGAGA | 54455 |
rs574086887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | FBXO42 | GRCh38.p7 | 1:16316547 | TCGAGACCAGCGTGG[A/G]CAACATGGCGAAATC | 54455 |
rs574119677 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16322567 | GGCAACAGAGCGAGA[A/C]TCTGTCTCAAAATAC | 54455 |
rs574137311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16335637 | TTGGGAGGCCGAGGC[A/G]GGTGGATCACCAGAG | 54455 |
rs574149325 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16291573 | TTTTAGTAGAGATGG[A/G]GTTTCGCTATGTTGG | 54455 |
rs574197845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16334953 | TAATAATGGCCACGC[A/G]CAGTGGTTCACACCC | 54455 |
rs574212150 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16323650 | CAAAAATTAGCCAGG[C/T]GTGGTGGTGTGCACC | 54455 |
rs574232945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16278919 | GAGCAGCTGGGACTA[C/T]AGGCATGTGCCACCA | 54455 |
rs574266112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16294320 | TGTAGAATCTTCCCA[C/T]ACCCCTGGGTTGTTA | 54455 |
rs574278346 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16319768 | ATACAAAAATTAGCC[A/G]GGCATGGTGCCGTGC | 54455 |
rs574331434 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16330843 | GCTACTCAGGAGGCT[A/G]AGGCAGGAGAATCAC | 54455 |
rs574349310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16296580 | GCTTGAACCCGGGAG[A/G]CGGAGGTTGCAGTGA | 54455 |
rs574409852 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16329413 | ACAGGGTGAAACCCC[A/G]TTTCTACTAAAATAC | 54455 |
rs574437673 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16295701 | CCCGGCCAATAAATG[A/C]ATCTTTATATGACAC | 54455 |
rs574467804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16331239 | TAACACGGTGAAACC[C/T]CGTCTCTACTAAAAA | 54455 |
rs574498785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16345107 | CCGTCTCAAAAAAAC[A/G]ACAACAACAAAAAAA | 54455 |
rs574510774 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16305281 | TGGGCCCAGCTACTC[A/G]GGAGGCTGAGGCAGA | 54455 |
rs574535776 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16352777 | TAACTCACTTCTACC[C/G]CGAGGGCCCGATGAG | 54455 |
rs574538722 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16334454 | AACAGACTGATTCTA[C/T]AGATAAGACTAATGA | 54455 |
rs574576957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16273867 | GCCTAGGCAACAGAA[C/T]GAGACTCTGTCTCAA | 54455 |
rs574600514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16287434 | TCTTCCTTCATTTGA[A/G]TGTAGTCTCATTAGG | 54455 |
rs574629092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16336444 | GCTCATTGCAACCTC[C/T]ACCTCCTGGGTTAAA | 54455 |
rs574631359 | snp | G/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251237 | TGTCTGTTCAGGAGG[G/T]TGTCTCATACTTCCC | 54455 |
rs574723255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16324389 | GACACATAAATTAAT[A/G]ATACCAACACAGAAC | 54455 |
rs574724456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16304583 | AAATACCCTCATGTA[C/T]AGCTTTCCTTTGTTT | 54455 |
rs574747566 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | FBXO42 | GRCh38.p7 | 1:16352443 | AACGCCGCCGCCGCC[A/G]CAGCTGCTGCTGCTC | 54455 |
rs574750783 | snp | C/T | 0 | 0 | intron-variant | FBXO42 | GRCh38.p7 | 1:16260907 | GGGGGTCTCTCTGTG[C/T]TGCCCAGACTGGTCT | 54455 |
rs574768155 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16344039 | TTTCACTCATGTTGC[C/T]AAGGCTGGAGTGCAA | 54455 |
rs574786185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16252577 | ATGCATCCACTTACG[C/T]TTTCATTCATTCATA | 54455 |
rs574869526 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16297611 | TCACGCCAGTAATCC[C/G/T]AGCACTTTGGGAGGC | 54455 |
rs574940784 | snp | A/G/T | 0.00755907 | 0.0610114 | intron-variant | FBXO42 | GRCh38.p7 | 1:16290385 | TAGCCCTCATAAGAT[A/G/T]AATCCCCTTATAAGA | 54455 |
rs574971685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16262500 | TCACTTGAGGCCAGG[C/T]GTTTGAAACCAGCCT | 54455 |
rs575002262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16311850 | TATGATCCAGCAATT[A/G]TGCATCTTGGTATTT | 54455 |
rs575034148 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16298123 | CCCAGCTACTGGGGA[G/T]GCTGAGGCAGTAGAA | 54455 |
rs575088758 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16311053 | GGGTCAACGCCGGGC[A/G]CGGTGGCTCACGCCT | 54455 |
rs575130265 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16259086 | AATCTGAAGTGCTGA[A/G]GTATTCTCTACCCTC | 54455 |
rs575196633 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16312624 | TCCAAACCCATAGAA[G/T]GCACAACACCAAGCA | 54455 |
rs575205741 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16354301 | GTGTGAGCCACGGCG[C/T]CTGGCCTTTTTATGT | 54455 |
rs575254947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16313403 | CCAAAATAAGACTGC[C/T]AAAGAAAACCTAAGG | 54455 |
rs575276572 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16254197 | TGCGGCCAGACACTA[A/G]TGCCTAATGAGATTA | 54455 |
rs575327674 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16262326 | AAATGCCTGGCTCAT[A/C]TTTCATACTTTGAAT | 54455 |
rs575384553 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16268775 | TCAAGATCAGCCTGA[A/C]CAACATGGAGAAACC | 54455 |
rs575393280 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16339533 | GGCCAGGATGGTCTT[C/G]ATGTCTTGACCTCAT | 54455 |
rs575412016 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FBXO42 | GRCh38.p7 | 1:16282466 | CCTGATCTCAGGTGA[C/T]CCACCCGCCTCGGCC | 54455 |
rs575467958 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16325312 | ACATTTTTTACCCAA[C/T]TGTTTTTAAGTACAC | 54455 |
rs575477158 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16283122 | GTTATCCAATTTTTA[C/T]GAACAGTAATTTTGT | 54455 |
rs575508508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16328001 | CCACTTTGCCCAGCC[A/G]GGACAGTCTGAAACA | 54455 |
rs575526634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16291155 | TCACAACTGACAGTG[C/T]CCTCCCCTCAGTCAC | 54455 |
rs575565877 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16285016 | CCGGGCGTGGTGGCA[C/T]GTGCCTGTAATCCCA | 54455 |
rs575600851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16342372 | TTGCACTCCAGCCTG[A/G]GCAAGAAGAGCGAAA | 54455 |
rs575637642 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16341926 | CGATGAGCCAAGATC[A/G]CGTCATTGTACTCAA | 54455 |
rs575660014 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16354202 | AGTAGAAAATACGGG[A/G]TTTCACCATCTTGGA | 54455 |
rs575678344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16277261 | ATTGCCACAAGATTT[A/G]GCATTCTCCTAACAC | 54455 |
rs575801417 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16270363 | CACTTCCAGTGTCTC[G/T]GCTAGATGGAGTTAG | 54455 |
rs575831293 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16315117 | TTGGAGTCTAAAAAT[A/C]AATCAGTGAAATTTG | 54455 |
rs575876418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16340375 | CTAGGCTAGAGTGAA[A/G]TAGTGCCATCTCGGC | 54455 |
rs575888721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16347718 | AAATTAGGCAGGCAC[A/G]GTGGCTCACGCCTGT | 54455 |
rs575908136 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16247181 | GAGGGAGCCACTTAC[C/T]GGTAACCATGCAGAA | 54455 |
rs575916698 | in-del | -/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16309970 | GGAGGCCAAGGCAGG[-/C]AGATCACAAGGTCAG | 54455 |
rs575946428 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16249099 | GATGTTTTGAAATTA[A/G]GATTTAAATTTCAAA | 54455 |
rs575976669 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16301843 | TAGAGATGTTGCCCA[A/G]ATTGGTCTCAAACAC | 54455 |
rs575996250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16266002 | TACTCTAGTCTTACA[C/T]ACTTCAGACTTTTGG | 54455 |
rs576028431 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16265337 | CTCAGGTGGTCCTCC[C/T]GTCTTGGCCCCCCAA | 54455 |
rs576065774 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16335533 | TCTATTCTTTATTTC[A/G]CTGTAGTATTAAACT | 54455 |
rs576104276 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16259082 | CATCAATCTGAAGTG[A/C]TGAGGTATTCTCTAC | 54455 |
rs576141083 | in-del | -/A/AA | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16342398 | GAAACTCTGTCTCAA[-/A/AA]AAAAAAAAAAAAAAA | 54455 |
rs576192216 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16271082 | TCACAAGGACATGCA[A/G]GAAGAGTGTTCCAGG | 54455 |
rs576253436 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16294471 | CGACTCTGTGTTTCT[G/T]TTCTTACTTCAACCT | 54455 |
rs576259149 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16308566 | GTGCAGTGGCACGAT[A/C]CCCGTTCACCACAAT | 54455 |
rs576272163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16263746 | AAAACAAAAAAAAAC[C/T]GAAAAACCAAAAAAC | 54455 |
rs576272531 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FBXO42 | GRCh38.p7 | 1:16336226 | TACAGGCATGAGCCA[C/T]CGCGTCTGGCCTAAT | 54455 |
rs576309523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16263338 | TTGTAGTCCCAGCTA[C/T]TCAGGAGGCTGAGGC | 54455 |
rs576360444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16273621 | CATGGTGGCTTATGC[C/T]TGTAATCGTAGCACT | 54455 |
rs576439691 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250594 | AATTTTGTTTTCCCA[A/G]TTCTCAGTCCAAATG | 54455 |
rs576443192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16281572 | CTCCCAGGTTCAAGC[A/G]ATTCTTGTGCCTCGG | 54455 |
rs576456362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16303240 | CATGCAGCACACTAA[C/T]GCTGAAGCTTGCTGA | 54455 |
rs576461908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16302736 | GCTGGTTTCAAACTC[C/T]TGACCTCAAGTGATC | 54455 |
rs576482491 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16350680 | TAAACCCAGGGGATG[C/G]AGATTGCAGAGAGCC | 54455 |
rs576490494 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16255362 | TTTTTTCCTTAAGAG[A/T]CTCGATCTGTTGCCC | 54455 |
rs576501025 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16348172 | ACTTTTCCATCAGCC[A/G]CAACTTTAGATCACT | 54455 |
rs576504618 | in-del | -/AAG | 0.00279162 | 0.0372561 | intron-variant | FBXO42 | GRCh38.p7 | 1:16323856 | GCAGAGAAAAATAAA[-/AAG]AAGAAGGGACTGGAC | 54455 |
rs576515329 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16322776 | GAGTAAGAAACAAAA[A/C]CCTCCCTAAGTAATG | 54455 |
rs576534265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16330108 | ATCACACAATGTAGC[C/T]AGACACTAAGCTAGT | 54455 |
rs576607957 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FBXO42 | GRCh38.p7 | 1:16265629 | ACACTGAGCTAGACA[C/T]TGTTCTAGGTACCTC | 54455 |
rs576662597 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16272812 | CTTCTAGCCTTTACA[A/C]GAACAATGGCTAGCA | 54455 |
rs576662712 | in-del | -/A | 0.498277 | 0.0293024 | intron-variant | FBXO42 | GRCh38.p7 | 1:16320360 | AGCAAACTCCATGTC[-/A]AAAAAAAAAAAAAAA | 54455 |
rs576677332 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | FBXO42 | GRCh38.p7 | 1:16281191 | GGTCTCGAACTCCTG[A/C]CCTCAGGTGATCCGC | 54455 |
rs576677429 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16289251 | AAAAAAGAAAGAAAA[G/T]AAAATGTCCCGATGT | 54455 |
rs576689214 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16323246 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 54455 |
rs576690008 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16272222 | ACAGCATGAAGTCTG[C/G]CCAGATGTCCACAGA | 54455 |
rs576716783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16331849 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGACCA | 54455 |
rs576727867 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16324606 | GCAGAAAACTTGAGT[A/C]CAGGAATTTGAGACC | 54455 |
rs576815642 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FBXO42 | GRCh38.p7 | 1:16331281 | AGCCGGGCATGGTGG[C/T]GGGCGCCTGTAGTCC | 54455 |
rs576853042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16274956 | ATGTAAAAGCTGGCA[A/G]TAAACTGTAAACCAT | 54455 |
rs576860419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16266960 | TTACTCAAAACTATT[C/T]TGATTTTACAGGCAA | 54455 |
rs576881656 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16325087 | TATAAAAAATACACA[A/C]GTTAGCCAGGCATGG | 54455 |
rs576898578 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16274456 | GTGAAGAAAGTTTTC[C/G]TATCTTGATCTAGGT | 54455 |
rs576902419 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16267951 | AACAAAACCATATGA[A/G]AGACCACTTGATGAA | 54455 |
rs576905300 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16340079 | CTCTTGGGAGGCTGA[C/G]GCAGAAGAATGGCGT | 54455 |
rs576950189 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16303815 | CAGTGGCGTGATCTC[C/G]GCTCACTGCCAGCTC | 54455 |
rs577079320 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16337035 | TGTCTTTCCAAACAC[A/C]AGTGCACATATTTTA | 54455 |
rs577083432 | in-del | -/TAT | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16330086 | TAGGTGAAGTTATTA[-/TAT]TATTATCACACAATG | 54455 |
rs577115561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16344084 | CTCACCGCAACCTCC[A/G]CCTCCCAGGTTTAAG | 54455 |
rs577117531 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16272549 | CAGGCGTGAGCCACC[A/G]TGCCCGGTGGGTCAC | 54455 |
rs577143309 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16256193 | CATTACAAGAAACGG[C/T]GGTTGCTGTCATTAA | 54455 |
rs577143826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16299001 | TTCAAAAAGGTAACA[A/G]ACATTTTTCCTTTTT | 54455 |
rs577160274 | in-del | -/AAACAAAC | 0.00280336 | 0.0373339 | intron-variant | FBXO42 | GRCh38.p7 | 1:16347519 | ACTTCCTCTCAAAAC[-/AAACAAAC]AAACAAACAAACAAA | 54455 |
rs577184668 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16275958 | ACAGAGTGAGACCCC[A/G]TCTCAAAATAAATAA | 54455 |
rs577185535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16254978 | CTTTACATGTGGCTC[A/G]ACCAACCTATCACAT | 54455 |
rs577216177 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16346368 | TTTATAGAAATTAAA[C/T]GAACTACTTCAAATC | 54455 |
rs577267599 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16306859 | AAACACCACCATGCC[C/T]GGCTAAAATGGATTA | 54455 |
rs577280169 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16260749 | CACCCAGGCTGGAGT[A/G]CAGTGGTGTGACTGA | 54455 |
rs577353648 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16254103 | CACTTAGGCTGTATC[C/T]TTCTTCCCCTACTTT | 54455 |
rs577367121 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16267720 | CATCAACATTCACTG[C/G]TATTAGACAAAACTT | 54455 |
rs577399452 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16331732 | GGGCAACAGAGCAAG[A/C]CTCAGTCTCAAAATA | 54455 |
rs577401246 | in-del | -/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16302067 | CTCTCACACAGATAA[-/T]TAATGGCAAAAGACA | 54455 |
rs577426519 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16353437 | TGGTAAGAAACATTT[A/G]CAATCTGTTCTCTCT | 54455 |
rs577430075 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16298165 | CGGGAGGTGGAGGTT[G/T]CAGCGAGCTGAGATT | 54455 |
rs577462878 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16291186 | CCTCCAATCTACCTA[C/T]CTCGATGCACTAAAA | 54455 |
rs577481002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16261276 | CATTTACTTATTCTC[C/T]GAACTCTCCAAGGAA | 54455 |
rs577488843 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16352826 | ATGTGAGTGCTCTTG[A/G]ATATCGCCAAGGGGA | 54455 |
rs577564571 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | FBXO42 | GRCh38.p7 | 1:16341572 | AAGATTGCACCCCTG[C/T]ACTCCAGCCTGGGCA | 54455 |
rs577569875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16270207 | CAGTCTAACCCATTA[A/G]TCCAGGAACGAATTA | 54455 |
rs577593447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16261767 | GGAGTGCAGTGGCGC[A/G]ATCTCGGCTCACTGC | 54455 |
rs577596709 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16321197 | AAAACATCAAACCCC[A/T]TACCTTTGAGGGCAT | 54455 |
rs577602593 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXO42 | GRCh38.p7 | 1:16306307 | CAGGCATGAGCCACC[A/G]CGCCCAGCCTATAAG | 54455 |
rs577630297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16300611 | CTGTCATGTGTCTCA[C/T]ACCTACAAGCCAGAA | 54455 |
rs577640769 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16278082 | CACATCCAGGCCAGG[C/T]GTGGTGGCTCATGCC | 54455 |
rs577674344 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16334088 | AGCTTATAATATGAA[A/T]TTCAGCTACCAGACA | 54455 |
rs577733313 | snp | G/T | 0.000399281 | 0.0141238 | missense, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16315325 | CCAATACTGGGTGGG[G/T]CTCCTCATCTTGATC | 54455 |
rs577751903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16278776 | AGTTATTTCTCTTTT[C/T]TTCTTTTTTTTTGAG | 54455 |
rs577772192 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16248071 | CTCATTTTTCTCAGT[C/G]AATTTTAAGACAAAA | 54455 |
rs577850110 | snp | A/C | 0 | 0 | intron-variant | FBXO42 | GRCh38.p7 | 1:16269671 | GCTGGGATTACAGGC[A/C]TGAGCCACCATGTCC | 54455 |
rs577877279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16285745 | AACGCTTTCCTCATA[C/T]GCTGGCTTCCCAGAT | 54455 |
rs577900156 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16323524 | GGACAGGGCCGGGCG[C/T]AGTGGCTCACGCCTG | 54455 |
rs577925311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16284005 | AATCAGTCTGAGTTT[A/G]AATAAAGGGTAATTT | 54455 |
rs577938605 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16341552 | GGCAGAGGTTGCAGT[A/G]AGCCAAGATTGCACC | 54455 |
rs577961928 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXO42 | GRCh38.p7 | 1:16325768 | GTAGCTGGGATTATA[A/G]GCATGCGTCACCACG | 54455 |
rs578032485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16263801 | AAACCCACGGCCATA[C/T]ATTAACTTTTTTTTT | 54455 |
rs578062356 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16271243 | ATCCCTAACTACTGT[G/T]TGCGTGTGTGTGTTG | 54455 |
rs578090358 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | FBXO42 | GRCh38.p7 | 1:16262993 | TAGGATTACAGGCGT[C/G]AGCCACAACTTTGGT | 54455 |
rs578105730 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXO42 | GRCh38.p7 | 1:16301254 | AGACTTTTCCATAGG[A/G]AAGATACTATACTGT | 54455 |
rs578141873 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16247271 | CTCACCACCAGGCGT[A/G]GTTAGATCCTCCCCA | 54455 |
rs578190027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16334232 | AGGTCAGGAGATCGA[A/G]ACCATCCTGGTTAAC | 54455 |
rs578244564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXO42 | GRCh38.p7 | 1:16334874 | TCCTTAAAGCAAATA[C/T]AAATTAAATGGAGTT | 54455 |
rs745377335 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16290719 | GAGATGCCAGAGCTC[A/T]CTCTCTGCTACATGA | 54455 |
rs745399404 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16341973 | AGAAATTCCGTCTCC[-/A]AAAAAAAAAAAAAAA | 54455 |
rs745427602 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16302916 | CCTCCCACCAGGTCA[C/T]TCCCTTGACACATGG | 54455 |
rs745432372 | snp | A/T | 1.73234e-05 | 0.00294302 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250647 | ATTAAAAGCCACAGA[A/T]AAGGAAAGGGGTTTA | 54455 |
rs745510639 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16294502 | CCTACCAAATGATGT[-/A]TCACACCTGTATGAG | 54455 |
rs745517660 | snp | C/T | 4.94173e-05 | 0.00497053 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250827 | ACCACAGAACTGCTA[C/T]TAAATACTTTCCATT | 54455 |
rs745523281 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16328192 | TTAAAAAAAACCACT[C/T]ACTCAGGAGGCTGGG | 54455 |
rs745555557 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16284248 | GGCCAGGATTTCCAA[G/T]GGTTTCTGTTCTACC | 54455 |
rs745643875 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16313073 | GTGCTGGGATTACAG[A/G]CGTGTTCCACTGTGT | 54455 |
rs745673268 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16247918 | TGACCAGTGAAGTCA[C/G]TAGGCCATGGGAGCT | 54455 |
rs745696818 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16280724 | AGGCTGCAGTGAGCC[A/G]ACATCCGCCACTGCA | 54455 |
rs745717475 | snp | A/G | 1.64852e-05 | 0.00287094 | missense, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16256745 | TTGCTCCAGCTTTGG[A/G]GGAAGGATAGGACCC | 54455 |
rs745719525 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16326848 | CATGGAGATGAGCTA[C/T]ATAAATGTCATCTAA | 54455 |
rs745736245 | snp | C/T | 1.6596e-05 | 0.00288058 | intron-variant | FBXO42 | GRCh38.p7 | 1:16294770 | AGGCAAAGATCAGCA[C/T]TTCATCTCTTACCTG | 54455 |
rs745749681 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16296650 | GCAAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 54455 |
rs745880705 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16261486 | TGGCCTATTTTATGT[C/T]ACAAAGTAGGAGCAT | 54455 |
rs745932620 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16307310 | TTGAGACCAGCCCGG[A/G]CAACATAGCAAGACC | 54455 |
rs745934070 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16274961 | AAAGCTGGCAGTAAA[A/C]TGTAAACCATGTTCA | 54455 |
rs745973777 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16288355 | GAATCACTTGAACCC[G/T]GGAGGTGGAGGTTGC | 54455 |
rs745999271 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16319865 | GCAGTGAGCCGAGAT[C/T]GCGCCACTGCCCTCT | 54455 |
rs746007367 | in-del | -/GTG | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16260752 | CCAGGCTGGAGTGCA[-/GTG]GTGTGACTGATCATG | 54455 |
rs746020818 | snp | C/G | 1.7653e-05 | 0.00297089 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16253143 | AGATAGTTGCATCAT[C/G]TATGACAATCTGAGG | 54455 |
rs746026413 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16287498 | CCCTGGCATATAGAA[A/C]AATACCAGGGGGGCA | 54455 |
rs746041307 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16332840 | GCCACTGCGCCTGGC[C/G]TCGACTAATGAATAT | 54455 |
rs746113374 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16254029 | ACTGTCTGAGGAGCT[A/G]ATATAAAATGAAGGG | 54455 |
rs746117922 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16331708 | TCAGTGAGCCGAGAT[C/G]GCACTACTGGGCAAC | 54455 |
rs746120201 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16292585 | TATAGGCGTGAGCCA[C/T]TTCGCCTAGCCACAA | 54455 |
rs746229485 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16300448 | TTCCAGTAGTTTCAT[A/C]TTTTCCATGGTGTAT | 54455 |
rs746239113 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16265940 | AAGCAGGTATATAAT[A/C]CTACCATTTTCTCAA | 54455 |
rs746282911 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16299322 | AGCCCACATTTTTCT[C/T]CTCTATTTGGACTGA | 54455 |
rs746306411 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16305680 | GATTATGCCACTGCA[C/T]TCCAGCTTGGGTGAT | 54455 |
rs746319102 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16312288 | GATGACTTGAGCCCG[C/G]GAGACGGAGGTTGCA | 54455 |
rs746367988 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16323569 | TGGGAGGCTGAGGTG[C/T]GCGGATCTTTTGAGG | 54455 |
rs746376998 | snp | C/T | 3.31279e-05 | 0.00406975 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251149 | TGATGGCTTCCAGAC[C/T]CCGACGCAGGGCACC | 54455 |
rs746380699 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16271235 | ATACTTTGATCCCTA[A/C]CTACTGTGTGCGTGT | 54455 |
rs746478399 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16268340 | TTTTCCCACTCTTCT[C/G]TTTAGCAGGAGGTAA | 54455 |
rs746490480 | snp | A/T | 1.64751e-05 | 0.00287007 | intron-variant | FBXO42 | GRCh38.p7 | 1:16305777 | CCACAGGCAGGGTGG[A/T]ATCTGCTTTCACAGT | 54455 |
rs746506235 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16254380 | GTCCAGGAGTTAAAA[G/T]CTTTATCGATTCTGG | 54455 |
rs746507976 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16282256 | TTTGAGACAGAGTCT[C/T]ACTCTGTCCCCCAGG | 54455 |
rs746548644 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16282371 | ACTGGGATTACAGGC[A/G]CCCACCACCATGCCC | 54455 |
rs746579780 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16342399 | GAAACTCTGTCTCAA[-/A]AAAAAAAAAAAAAAA | 54455 |
rs746580367 | snp | C/T | 1.74735e-05 | 0.00295575 | intron-variant | FBXO42 | GRCh38.p7 | 1:16315130 | ATAAATCAGTGAAAT[C/T]TGAAATCAATAAATA | 54455 |
rs746600482 | snp | C/T | 1.67281e-05 | 0.00289202 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251773 | GGCTGAAGACCACCA[C/T]ACACTGTCCCACCTG | 54455 |
rs746601464 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16280527 | ACCGCAATTACTTTT[A/G]CACCAACCTAATAAT | 54455 |
rs746620725 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16326627 | AGGTAGAGGTTGCAG[C/T]GAGCCAAGATCACAC | 54455 |
rs746627198 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16313914 | AAAATACAGCATGTC[C/T]AGCACCTAAACATTT | 54455 |
rs746636562 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16345847 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 54455 |
rs746644243 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16325294 | AAAACTAAACTAAAA[A/G]ACACATTTTTTACCC | 54455 |
rs746674766 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16276272 | GTAGTCCCAGCTATT[C/T]GGGAGGCTGAGGCAG | 54455 |
rs746706610 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16312483 | AAAACTATGGAGACA[A/G]TAAAAAAATCAGTGA | 54455 |
rs746708876 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16247843 | TGTGAAATAAGAGAA[C/T]AGGAAGCTCTGTCCA | 54455 |
rs746733928 | snp | C/T | | | downstream-variant-500B | FBXO42 | GRCh38.p7 | 1:16246408 | GAGATGGGGTCTCAC[C/T]ATATTGCCCAGGCTG | 54455 |
rs746793864 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16294544 | AAACCATGCAAATGA[A/G]TTCACACAGCAGTAC | 54455 |
rs746796003 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16339339 | GTTTTTTTGAGATGA[A/C]GTCTCACTGTGTTGC | 54455 |
rs746865822 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250772 | GATGAGTTCACCCCT[A/G]CCTTGTACCACGGTA | 54455 |
rs746876941 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16319520 | AAGTCCACCTGGTGG[A/T]ATGGGGGAAAGGCAC | 54455 |
rs746902510 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16306184 | CTGCCACCATGCCCA[A/G]CTAATTTTATTTTTA | 54455 |
rs746908435 | snp | G/T | | | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16354273 | TCGGCCTTCCAAAGT[G/T]CTGGGATTACAGGTG | 54455 |
rs746952518 | snp | A/C/G/T | 8.2416e-05 | 0.00641893 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16256743 | AGTTGCTCCAGCTTT[A/C/G/T]GGGGAAGGATAGGAC | 54455 |
rs747021465 | in-del | -/AAAC | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16347515 | AGAGACTTCCTCTCA[-/AAAC]AAACAAACAAACAAA | 54455 |
rs747023893 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16273499 | ATGAGTGCATATATC[C/T]ACTGAAAAGTACAAA | 54455 |
rs747078718 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16322232 | GCCTGAGAGTCTGCT[A/G]CCAGAGAGGAAACTA | 54455 |
rs747103633 | snp | C/T | | | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16318549 | TACAAAGAAAGCATA[C/T]ACATAGAGGCAGGCA | 54455 |
rs747142015 | snp | A/T | 6.59903e-05 | 0.00574376 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251393 | CAAAGAAAGTCCTAT[A/T]TTCAGGTCGTATCCT | 54455 |
rs747210971 | in-del | -/G | 1.64947e-05 | 0.00287177 | frameshift-variant, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251370 | GTAGTGATCCTCGTC[-/G]GGGGGGCCAAAGAAA | 54455 |
rs747265360 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16265768 | GAAGTTTAGGTTCAG[A/G]TAAGTCCCTATTAAA | 54455 |
rs747361954 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16312256 | GGTCCCAGCTATTCT[A/G]GTGGCTGAGGAGGGA | 54455 |
rs747403247 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16277276 | GGCATTCTCCTAACA[C/T]ATTTGCATATTATAA | 54455 |
rs747404514 | snp | C/T | 3.29701e-05 | 0.00406005 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250965 | GGGTGGTGGCCCAGG[C/T]GGCGAGCAATGGGAG | 54455 |
rs747431385 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16310570 | GAATTCATTAAAACT[A/G]AAAGTTTCTGCTCTG | 54455 |
rs747435768 | snp | C/T | 1.69149e-05 | 0.00290812 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16253107 | TCACAGCATTGGGAC[C/T]GCCACACCCTCCGAG | 54455 |
rs747452132 | snp | A/C | 5.07318e-05 | 0.0050362 | intron-variant | FBXO42 | GRCh38.p7 | 1:16253607 | ACGCTACAGTGTTTG[A/C]TGAATAGTTATTTTA | 54455 |
rs747453998 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16291537 | AGGCACATGCCACCA[G/T]GCCCTGCTAATTTTT | 54455 |
rs747466157 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16322615 | CTAAAAAAAAAACTA[C/T]GCTACATATAACTAA | 54455 |
rs747472038 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16336302 | CTTCAGCCAAATGAT[C/T]GTAATATTCTCTCTT | 54455 |
rs747476220 | in-del | -/AAAAAAAAAAAAAAAAAAACA | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16301687 | AAAAAAAAAAACAAC[-/AAAAAAAAAAAAAAAAAAACA]AAAAAAAAAAGAAAC | 54455 |
rs747500911 | in-del | -/GGCT | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16303173 | TGCAGCAGTGAGTCA[-/GGCT]GAAAAGGCAAGCCAG | 54455 |
rs747571092 | snp | C/T | 4.95462e-05 | 0.00497701 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251045 | TGTTTCTCCACTGCT[C/T]AAACTCTGGCTCCCA | 54455 |
rs747594196 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16322291 | CCGAAAAACTACTAT[-/A]ACTAGGCCAGGCGTG | 54455 |
rs747598609 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16313745 | AGATTGTTCTCTGTT[A/G]TATCTCTGGCTGCCT | 54455 |
rs747696294 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16336649 | GGCATGAGCCACTGT[C/T]CCTAGCTGGGCCAAG | 54455 |
rs747696596 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16294214 | GTTTTTATTTTTTCC[A/C]CCAGGAGAGGTTAGG | 54455 |
rs747704183 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16325211 | CCACTGCACTCCAGC[C/T]TGGGCAACAGAGCAA | 54455 |
rs747758391 | snp | A/G | 1.64866e-05 | 0.00287106 | stop-gained, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16294798 | CTGAAGCCAAAGGTC[A/G]GATCCACTCTTTGCT | 54455 |
rs747774802 | snp | C/G/T | 8.27594e-05 | 0.00643224 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251543 | TCTGGCTGGGGAAAG[C/G/T]CTCCCTTCCCGGGAA | 54455 |
rs747795180 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16338891 | TCGCGGCTCACTGCA[A/G]CCTCCGCCTCCCAAA | 54455 |
rs747814327 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16337149 | GAAATCTCATTCAAT[A/G]TCTCCTAAGGTTCCA | 54455 |
rs747877016 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16338954 | TAGCTGGGATTACAG[A/G]TGCACATCATCACCC | 54455 |
rs747941788 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16271810 | TGTTACTTAGTACTA[C/T]ACCTGCATACCTAGC | 54455 |
rs747956694 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16291833 | CATGCCATCATGCCC[A/G]GCTCATTTTTAATTG | 54455 |
rs748005794 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16304987 | AGAAAAAGCAGAATA[C/T]AAAATTCTTAACAAA | 54455 |
rs748011292 | in-del | -/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16269107 | AGCCACCGCACCTGG[-/C]TTTTTTTTTTTTTGT | 54455 |
rs748018466 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16254726 | TCCACTTCAGAGCAC[-/A]GGGGGAATGACCACA | 54455 |
rs748022743 | snp | C/G | 1.64977e-05 | 0.00287203 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251738 | ACTGGGGCTGAGTGG[C/G]GCTCTCCCACTAGGA | 54455 |
rs748023826 | in-del | -/TACTGTTAC | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16254004 | TCTCTAAAATGAAAA[-/TACTGTTAC]TACTGTCTGAGGAGC | 54455 |
rs748035926 | in-del | -/TG | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16282120 | TTACTGTAATAACAC[-/TG]TGAGAGAGCTCACAT | 54455 |
rs748049114 | in-del | -/CG | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16350545 | CAGCCTGGGCAACAT[-/CG]GTGAAACCCCGTCTC | 54455 |
rs748056648 | in-del | -/AAA | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16313361 | AAGAAAGAAAGAAAG[-/AAA]GAAAGAAAGAGAAAA | 54455 |
rs748118919 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16330002 | GATTTCCAAATAATT[C/T]GTGTATGTACGTTTT | 54455 |
rs748143826 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16286259 | AGTCTATTCTCACAG[G/T]GCTATGAAGAAATAC | 54455 |
rs748168388 | in-del | -/TCC | | | cds-indel, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16247542 | GTTGGTTTTCTTTCT[-/TCC]TCCTCCTCCTCCTCT | 54455 |
rs748175037 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16315930 | AATCCCAGCACTTTG[A/G]GAGACCGAGGCGGGC | 54455 |
rs748192955 | snp | C/T | 1.85472e-05 | 0.0030452 | intron-variant | FBXO42 | GRCh38.p7 | 1:16255676 | CCAGGAGTATTTACC[C/T]TCAGGCTCATATGGA | 54455 |
rs748196905 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16284797 | ACATGGAGAAACCCT[A/G]TCTCTACTAAAAAAT | 54455 |
rs748223701 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16348625 | AGAATCGCTGGAACC[C/T]GGGAGGTAGAGGTTA | 54455 |
rs748231247 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16298800 | TAGGCGTGAGCCACC[A/G]CGCCCGGCCAATGTC | 54455 |
rs748243228 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16264548 | AGTTCCCATCAAGCA[A/C]GACAGGACCAAATGT | 54455 |
rs748270711 | in-del | -/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16308494 | TGAGACCCATCTCTC[-/T]TTTTTTTTTTTTTTT | 54455 |
rs748281060 | snp | A/G | 3.31235e-05 | 0.00406948 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251169 | CGCAGGGCACCTGGG[A/G]AGACGGCCCCTGCAA | 54455 |
rs748282671 | snp | C/T | 4.66494e-05 | 0.00482934 | intron-variant | FBXO42 | GRCh38.p7 | 1:16255872 | GCACCACACACTTTA[C/T]GTAAAAATAGTAAGT | 54455 |
rs748299072 | snp | A/G | 1.64931e-05 | 0.00287163 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251246 | AGGAGGGTGTCTCAT[A/G]CTTCCCCCAACTGTC | 54455 |
rs748336164 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16342725 | CACCAAAACTCATGT[A/G]GAAATTTGATCCCCA | 54455 |
rs748375583 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16277212 | TGTTATACTGTCTGA[C/T]ATTCAGCAGTTAATC | 54455 |
rs748406392 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16267870 | TGAGAAACTTTTAGA[C/T]CTTATCTAACTATGC | 54455 |
rs748496588 | snp | C/T | 3.34778e-05 | 0.00409119 | intron-variant | FBXO42 | GRCh38.p7 | 1:16315166 | TTCTCCTATCCACAG[C/T]ACCTTTGATAAGTCG | 54455 |
rs748514730 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16300081 | TGAACCTTTTAGGAA[A/G]AAGAATTTGAGCAAC | 54455 |
rs748516763 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16322569 | CAACAGAGCGAGACT[C/G]TGTCTCAAAATACAA | 54455 |
rs748533808 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16309314 | AATCTCTTGACCTCA[C/T]GATCCACCCACCTTG | 54455 |
rs748537635 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16332399 | CAAAAAAAATGCTTA[C/T]GGAATTGATTAAAAG | 54455 |
rs748543088 | snp | C/T | 3.30191e-05 | 0.00406306 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16252368 | GCCAGGCCCAAGGAC[C/T]AGAATGCATGTGCAA | 54455 |
rs748546907 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16288642 | CCTTGATTGGCCTTC[C/T]CATGCTCCTAAATCT | 54455 |
rs748570308 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16321545 | CTCAGCTTCCCCAAC[A/G]TGACTGAATGAATGT | 54455 |
rs748570490 | in-del | -/AAAGG | 1.73421e-05 | 0.00294462 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250647 | ATTAAAAGCCACAGA[-/AAAGG]AAAGGGGTTTAGAAC | 54455 |
rs748599671 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16302881 | ACAGCATGGAGGAAA[C/T]CGCCCCCATGATCCA | 54455 |
rs748604831 | snp | C/T | 3.29625e-05 | 0.00405958 | missense, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16315376 | TTTCTTCCTGGTCCA[C/T]AGCCATGAAACTGTC | 54455 |
rs748612579 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16349522 | ATCCACATTAACAAT[C/T]GTGGGAAGGGCTTTA | 54455 |
rs748761342 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16277500 | GGGGCCGAGGCAAGC[A/G]GATCACTTGAGCTCA | 54455 |
rs748817529 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16258282 | AACAATACGATTTAC[C/T]GAGAAGGCATCAGTC | 54455 |
rs748855165 | in-del | -/GTAAT | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16351389 | CAGCAAGTAAAACTG[-/GTAAT]GTGTCAGAATCTTCA | 54455 |
rs748875861 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16270703 | AAAAAAAAAGAAAAG[-/A]AAAGAAAGAAGAAAA | 54455 |
rs748877277 | snp | C/G | 6.59163e-05 | 0.00574054 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250929 | TGGTATAGGGGTTTG[C/G]CAACATTTAGGGACT | 54455 |
rs748895242 | snp | A/G | 4.95471e-05 | 0.00497705 | intron-variant | FBXO42 | GRCh38.p7 | 1:16256781 | AAAGTCAGTAACACC[A/G]TGGTTAGCATTCAGG | 54455 |
rs748908490 | snp | A/G | | | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16352570 | CCAGGGGGCGGCGCA[A/G]TGTTGAGAAAGGCCG | 54455 |
rs748912431 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16336419 | GCTGGGGAGCAGTGG[C/T]GTGATCTTGGCTCAT | 54455 |
rs748922994 | in-del | -/AC | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16270753 | CTTACCATGAGATAC[-/AC]ACACACACACACACA | 54455 |
rs748929089 | snp | C/G | 1.65512e-05 | 0.00287669 | intron-variant | FBXO42 | GRCh38.p7 | 1:16294778 | ATCAGCATTTCATCT[C/G]TTACCTGAAGCCAAA | 54455 |
rs749023219 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16303288 | AGTTGCATGTTTCAG[A/T]CTTGCAGTATTTCCC | 54455 |
rs749066886 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16284647 | CCAGCCTGGCCAAGA[C/T]AGTGAAACCCCATCT | 54455 |
rs749080259 | snp | A/G | | | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16317140 | TACAAAAATTAGGCC[A/G]GGCGCAGTGGCTCAC | 54455 |
rs749084845 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16261686 | CAGCAACCAGAAGTC[-/A]AGGATACAGGTATAT | 54455 |
rs749133365 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16316344 | ATCTCTTTTGTTACT[A/G]TTTTCACATCGCTCT | 54455 |
rs749145312 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16329819 | CTGGGCATGGTGGTG[C/T]GCACCTGTAAGCCCA | 54455 |
rs749154129 | in-del | -/CAGA | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16313369 | AGAAAGAAAGAAAGA[-/CAGA]AAGAGAAAAGAAAGA | 54455 |
rs749155900 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16248178 | CCTTGGCCGAGACAC[A/G]TGAAGTCCCACCGCA | 54455 |
rs749157822 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16287875 | GATCGCCTGAGGTCA[A/G]GATTAACCTCAGGTG | 54455 |
rs749167525 | snp | A/G | 0.000132251 | 0.00813069 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251593 | GAGCCCTGGGTCTCA[A/G]TGTTCCCCAGCGGCC | 54455 |
rs749252197 | in-del | -/AAC | | | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16316864 | GCAGTAAAAAACTAG[-/AAC]AACATGAATGTCTAT | 54455 |
rs749319926 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16342864 | TCTCCGAAACTAGAT[C/T]AGTTCCTGGGAGAGT | 54455 |
rs749366584 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16310102 | CGGGAGGCTGAGGCA[A/G]GAGAATGGCGTGAAC | 54455 |
rs749390223 | snp | A/G | 4.95471e-05 | 0.00497705 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16253681 | GGGCCAGAGATGTTC[A/G]GCTTGGACCACGCCC | 54455 |
rs749398595 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16340563 | ACCTCAAGTGATCCA[C/T]CCACCTTGGCCTCCC | 54455 |
rs749463542 | snp | C/T | 7.24559e-05 | 0.00601853 | intron-variant | FBXO42 | GRCh38.p7 | 1:16253783 | AGCTCCCAGGGACCA[C/T]AATGGTGGCTGGGGA | 54455 |
rs749530837 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16320082 | AAACGTACAGTCGCC[A/G]AGCATGGTGGCTCAC | 54455 |
rs749613001 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16255480 | ACTGGGACTACAGGT[A/G]TGTGCCACCATGCCC | 54455 |
rs749637398 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16288511 | ATGAATTACTAGATA[C/T]TACTACTTAAACATT | 54455 |
rs749653497 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16326786 | CGTAAGCCAGAATCA[A/G]CTACACCTTTCATTA | 54455 |
rs749676066 | in-del | -/AAA | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16342397 | GCGAAACTCTGTCTC[-/AAA]AAAAAAAAAAAAAAA | 54455 |
rs749696167 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16287635 | TCTTGCTATGTTGCT[C/T]AGGCTGGTCTTGAAC | 54455 |
rs749703006 | snp | G/T | 3.44465e-05 | 0.00414995 | intron-variant | FBXO42 | GRCh38.p7 | 1:16315150 | ATCAATAAATAAACC[G/T]TTCTCCTATCCACAG | 54455 |
rs749727898 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16247051 | CCAGCTTCGCCAGGG[C/T]ACATGGGGTGTGCAC | 54455 |
rs749730997 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16349310 | TACATAGCACTTAAC[A/G]GGTTTCCTTGTCTGG | 54455 |
rs749765783 | in-del | -/CTT | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16340927 | TCTTTCAGCCCAGCA[-/CTT]CTTCTATTGTACCAT | 54455 |
rs749828751 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16267144 | TCCAAAATACTGCAG[C/T]CCAAGGACCAAGGGG | 54455 |
rs749829689 | snp | A/G | 1.70775e-05 | 0.00292207 | intron-variant | FBXO42 | GRCh38.p7 | 1:16251803 | GGAAGACAAAGGACC[A/G]GTGCTCACACTCTTC | 54455 |
rs749839478 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16346213 | AAAAGTAAACACCCT[A/G]CCTTATTAGAGATCA | 54455 |
rs749903125 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16286985 | TAGATTATGCTACCA[A/C]CTTTTAACTGGTCTC | 54455 |
rs749908542 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16285855 | GACTCAATCCTTACA[A/C]CATTCTCTTTTTTGT | 54455 |
rs749947429 | snp | A/G | | | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16316914 | AATTGTGGTACATTC[A/G]CCATGAAATATAGAG | 54455 |
rs749955149 | snp | C/T | 1.64811e-05 | 0.00287059 | missense, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16315346 | CATCTTGATCCATTG[C/T]CCCTTCCAGCACAGT | 54455 |
rs749964611 | in-del | -/T | 1.65231e-05 | 0.00287424 | intron-variant | FBXO42 | GRCh38.p7 | 1:16256790 | ACACCATGGTTAGCA[-/T]TTCAGGATCTCACAA | 54455 |
rs750051864 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16345240 | CAGCCTGGCCAACAT[A/G]GTGATACCCCATCTC | 54455 |
rs750121055 | snp | A/G | 1.64849e-05 | 0.00287092 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250969 | GGTGGCCCAGGCGGC[A/G]AGCAATGGGAGGTAA | 54455 |
rs750123310 | snp | A/G | | | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16317783 | TAATTAACCGGGTGT[A/G]CTGGCACACATCTGT | 54455 |
rs750173320 | in-del | -/TAGC | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16339871 | AGGTAGAGGATCACT[-/TAGC]TAGCCTGGGAAATCC | 54455 |
rs750189650 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16264225 | CAGTTATAGCACATA[C/G]GTTTAATACATTTTT | 54455 |
rs750195923 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16262430 | GGTGAGATCACATGG[A/G]GTGTGGTGGCTCAAG | 54455 |
rs750199854 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16297559 | TGGTATCCCCAGAAC[A/T]CTACTAAGAAGTCAA | 54455 |
rs750257769 | snp | A/G | 1.64993e-05 | 0.00287218 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251021 | AGGCCCTGGGCGAGG[A/G]ATGGGCACTGTTTCT | 54455 |
rs750263901 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16269559 | AGACAGAGTTTCGCT[C/T]TTGTTGCCCAGGCTG | 54455 |
rs750339116 | in-del | -/AATA | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16302089 | CAAAAGACAGATGGT[-/AATA]AATAATGGAGGAAGG | 54455 |
rs750411954 | snp | A/G | 4.98343e-05 | 0.00499146 | intron-variant | FBXO42 | GRCh38.p7 | 1:16294922 | ATAGCATGCACCTAG[A/G]AAGAAAATACACAAA | 54455 |
rs750456676 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16291016 | ATCAAGACTCTCCAC[A/T]CCCAACCAAAAGTGT | 54455 |
rs750467208 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16335540 | TTTATTTCGCTGTAG[C/T]ATTAAACTTCATGAT | 54455 |
rs750493663 | in-del | AAAATTTT/GAGCGAAACTCTGTC | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16342380 | CAGCCTGGGCAAGAA[AAAATTTT/GAGCGAAACTCTGTC]TCAAAAAAAAAAAAA | 54455 |
rs750511819 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16290016 | TCTTTCCCGTTACAA[C/T]ATAAGCTCCATGAGG | 54455 |
rs750560190 | snp | C/T | 1.65436e-05 | 0.00287602 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251577 | GAAGGAGTCTGCCTT[C/T]GAGCCCTGGGTCTCA | 54455 |
rs750564873 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16302434 | GCCTCAGGAAACTTA[A/C]ATTTATGGTAGAAGG | 54455 |
rs750566523 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16333972 | CTGTATCAACTGTAC[A/G]GTAAAAATAATAATC | 54455 |
rs750606331 | in-del | -/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16350544 | CAGCCTGGGCAACAT[-/C]CGGTGAAACCCCGTC | 54455 |
rs750621958 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16349208 | GGCAGACTCTGCAGA[A/G]TAATAGGAAAGGTTG | 54455 |
rs750623166 | in-del | GTTTTTTCTG/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16269844 | CTTTATGTTTTCTTT[GTTTTTTCTG/T]TTTTGTTTTGTTTTG | 54455 |
rs750643686 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16255383 | TCTGTTGCCCAGGCT[A/G]GAATGCAATGGGGTG | 54455 |
rs750686100 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16267923 | TTCTCTATTGGCATT[C/G]TTTTCACTTCTTAAC | 54455 |
rs750707786 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16281580 | TTCAAGCAATTCTTG[C/T]GCCTCGGACTCTTGA | 54455 |
rs750748603 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16314992 | GGATTAGATACTTCA[A/G]TATTCAAGCTGTTCA | 54455 |
rs750751658 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16311261 | GTGGTAAGATTGCTT[A/G]AGCCCAAGAGTTCAG | 54455 |
rs750762144 | in-del | -/TT | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16304115 | CAGCCAAATTTGTAT[-/TT]TTTTTTTTTTTTTTT | 54455 |
rs750786657 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16327722 | TTGTTTTGTTTTTTA[A/G]GACGGAGTCTCGCTC | 54455 |
rs750793659 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16325877 | GTGATCTGCCCACCT[C/T]GGTCTCCTAGAGTGC | 54455 |
rs750855921 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16314140 | TATTTTTAGTAGAGA[C/G]AGGGTTTCACCATGT | 54455 |
rs750861928 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16338174 | TGAGGCAGGAGAATG[C/G]TGTGAACCTGGGAGG | 54455 |
rs750938673 | snp | A/G | 1.83643e-05 | 0.00303015 | intron-variant | FBXO42 | GRCh38.p7 | 1:16255834 | CACCTAATGTAAAAA[A/G]ACAGGAGGAAGTCAA | 54455 |
rs750983267 | snp | A/G | 1.65433e-05 | 0.002876 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251200 | GGGCACTGGCCACGT[A/G]AGGTGGGGTATGCAC | 54455 |
rs750986766 | snp | A/C | | | intron-variant, utr-variant-5-prime | FBXO42 | GRCh38.p7 | 1:16261034 | AAAGTCAGAATATAT[A/C]ATGCTGCACTTCATG | 54455 |
rs750988189 | in-del | -/AAAAGAAAGAAAG | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16350757 | GCAAAAAAAAAAAAA[-/AAAAGAAAGAAAG]AAAGAAAGAAAGAAA | 54455 |
rs751076545 | snp | A/C | 1.64781e-05 | 0.00287033 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251323 | GATCCCAATTCAGAT[A/C]TATGGATCCTAATCT | 54455 |
rs751088789 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16347155 | CTGTGTGTGTGTGTG[C/T]GCATCAAAGCATCAC | 54455 |
rs751111013 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16309855 | TTGAGACCAGCCTGG[A/T]CAACATGGTAAAACC | 54455 |
rs751120942 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16341344 | CCGTGGCTCATGCCT[A/G]TAATCCCAACACTTT | 54455 |
rs751146684 | snp | A/C/T | 3.2948e-05 | 0.00405871 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16315269 | CAAAACCTCTTCTGG[A/C/T]AGCTCCGACATGGAC | 54455 |
rs751234655 | snp | C/T | 1.64909e-05 | 0.00287144 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16252338 | CATGCTCTTCATTTT[C/T]TACCTTGAGTGGCTG | 54455 |
rs751275208 | in-del | -/G | 9.74573e-05 | 0.00697991 | intron-variant | FBXO42 | GRCh38.p7 | 1:16255853 | GGAGGAAGTCAAGAA[-/G]TCAGCACCACACACT | 54455 |
rs751309965 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16261406 | CCTTTTAGAAAGGCA[A/C]AATCTTTCCCTCTAC | 54455 |
rs751314837 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16275543 | AGGATCGCTTGAGCC[C/T]AGGAATTTGAGGCTG | 54455 |
rs751322427 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16298546 | ATGGAGTCTCACTCT[A/G]TCACCCAGGCTGGAG | 54455 |
rs751344769 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16322060 | CTGTAATCCCAGCTA[C/T]CTGGGACATGTAAAA | 54455 |
rs751371639 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16289508 | AATAAGCTTGCTCCT[A/G]TCTTTATCTCAACTC | 54455 |
rs751399888 | snp | A/C | 1.6736e-05 | 0.0028927 | intron-variant | FBXO42 | GRCh38.p7 | 1:16252454 | GTGATATGCGTTCCA[A/C]AACACACACACACAG | 54455 |
rs751414851 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16321109 | ACAATAGCAAGCCAA[C/G]ATAAAGAGACTCATA | 54455 |
rs751427290 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16262908 | TAGAGACAGCATTTC[A/C]CCATGTTGTGTAGGC | 54455 |
rs751439699 | snp | A/T | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250888 | TGTCCAGCACGTACA[A/T]CTGCATGGGCTTGCA | 54455 |
rs751451272 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16333710 | AAAATGCACAGCCAC[A/G]AGTTTGCTTTAAGGA | 54455 |
rs751496952 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16255128 | TGGCCTTCTGCAGGC[A/G]CAGCACAGCAGGCAA | 54455 |
rs751505270 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16288161 | ACAATAATAATAGGC[C/T]GGGTGCAGTGGCTCA | 54455 |
rs751516721 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16329449 | ATTAGCCAGGCGTGG[C/T]GGTGTGCGCCTGTAG | 54455 |
rs751556500 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16267733 | TGGTATTAGACAAAA[C/T]TTGTCTGGATCTCAG | 54455 |
rs751621831 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16253787 | CCCAGGGACCATAAT[C/G]GTGGCTGGGGAGTTC | 54455 |
rs751647237 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16278719 | AAGGTATCATTTACA[A/C]TGTAAAAGAAACAGT | 54455 |
rs751648422 | snp | A/G | | | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16354244 | CAAACTCCTGAACTC[A/G]TGATCCACTCACCTC | 54455 |
rs751657696 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16301176 | AGTGTTGGGATTACA[C/G]GGGTGAGCCTCTGCA | 54455 |
rs751706756 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16300207 | ACAGTTACAGCTCAC[A/G]GTACAGTATGAATAC | 54455 |
rs751709879 | snp | C/T | 1.67981e-05 | 0.00289806 | intron-variant | FBXO42 | GRCh38.p7 | 1:16294746 | TGCCAAGGGAGTCAC[C/T]TGGTAAGGAGGCAAA | 54455 |
rs751728323 | snp | C/T | 1.64874e-05 | 0.00287113 | missense, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16294886 | GCCTCCAAACACATA[C/T]ATAGACTGATTAGCA | 54455 |
rs751803662 | snp | C/T | 4.97352e-05 | 0.00498649 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251480 | GCCACCCACAGCTGC[C/T]GTTCCTGGAGACAAA | 54455 |
rs751819976 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16311049 | AAATGGGTCAACGCC[A/G]GGCACGGTGGCTCAC | 54455 |
rs751826001 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16247127 | GTACAATGGAGCCAA[C/T]ACCTAAAGTTTGCTC | 54455 |
rs751834678 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16258587 | GTCTCGAACTCATGG[A/G]TTCAAGCAATCCTGC | 54455 |
rs751895131 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16278421 | CAATGTTAGCACCGA[C/T]GTTTGGGACCTGAGC | 54455 |
rs751952140 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16292606 | CTAGCCACAAAGCAG[C/T]CTTTAAACTTGATGG | 54455 |
rs751983204 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16340093 | AGGCAGAAGAATGGC[C/G]TGAACCCGGGATGCG | 54455 |
rs752075578 | snp | C/G | | | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16352524 | GGACGCGCGCGCACT[C/G]ACGTCAGCGCGGCGG | 54455 |
rs752096489 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16259214 | CTAGCCCAATTAGAA[A/G]GCCTAAGTAATATAA | 54455 |
rs752130585 | in-del | -/TT | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16346754 | GTACTGAACAGTACA[-/TT]TTTTTTTTTTTTTTT | 54455 |
rs752135309 | snp | C/T | 1.71968e-05 | 0.00293225 | intron-variant | FBXO42 | GRCh38.p7 | 1:16253760 | ACAGAAGGATAAAGG[C/T]AGTTAGGAGCTCCCA | 54455 |
rs752149387 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16258204 | TTAATGGTGTCACTT[A/T]CAAAGTCTCAAGGTT | 54455 |
rs752155549 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16272539 | GCTGGGATTACAGGC[A/G]TGAGCCACCGTGCCC | 54455 |
rs752162530 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16261306 | AAGGTAAGCTGAGGC[A/C]AGTGATAATGATAAA | 54455 |
rs752191014 | snp | A/G | 1.65581e-05 | 0.00287728 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251130 | CCTTTGGAGGACATC[A/G]CTTTGATGGCTTCCA | 54455 |
rs752197132 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16340036 | CAAAAAATTAGCCAG[A/G]CGTGGTGGCAGGCGC | 54455 |
rs752221631 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16320909 | ACTTTGGCTGCATGG[C/T]TGACATTTAAATTAA | 54455 |
rs752246907 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16341087 | TGTTCCAATATGGAA[C/T]GATCTCCAAAATATA | 54455 |
rs752297056 | snp | C/T | 1.67981e-05 | 0.00289806 | missense, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16255796 | CCATGGGAGGTGGCC[C/T]ATGGGTTGTCACAAT | 54455 |
rs752384831 | snp | C/T | 1.65507e-05 | 0.00287664 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251191 | CCCCTGCAAGGGCAC[C/T]GGCCACGTGAGGTGG | 54455 |
rs752412953 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16274794 | ACAGGGTTTCATCAC[A/G]TTGGCCAGGATTCTC | 54455 |
rs752439324 | in-del | -/TAATCACACCACACTT | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16343928 | GGCTGCATTGAGCCA[-/TAATCACACCACACTT]TAGCATGGCAAAAAA | 54455 |
rs752465859 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16288019 | GGTGTGGTGGTGGGC[A/G]CCTGTAATCTCAGCT | 54455 |
rs752466076 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16273066 | TCAACTTCATCATCA[C/G]TTCCCAGAAACCCTC | 54455 |
rs752483379 | snp | A/G | 1.64757e-05 | 0.00287012 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16315209 | GCAGACAAGGGCCGC[A/G]GTTTTGTGTTCCTGA | 54455 |
rs752518927 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16287225 | TCTGGGTCTTTGCAC[C/T]GATTATTCTCTGTTT | 54455 |
rs752558081 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16329088 | GAATTGCTTGAACCC[A/G]GGAGGCGGAGGTTGC | 54455 |
rs752565685 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16301023 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGATTAC | 54455 |
rs752571195 | snp | A/C | 1.64969e-05 | 0.00287196 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16252294 | CCTGCTTACCCGGCA[A/C]GCTGGATGGCACCAC | 54455 |
rs752666234 | in-del | -/T | | | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16354099 | TTCAACCGATTCTCC[-/T]GCCTCAGCCTCCCGA | 54455 |
rs752667283 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16279381 | GCTGCAGTGAACTAG[A/G]ACCTATGACTGAGTC | 54455 |
rs752670963 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16253522 | AAAAAAGAATGATAC[A/G]TTTTCTTTGGCTTAG | 54455 |
rs752694573 | snp | C/T | 1.64732e-05 | 0.0028699 | intron-variant | FBXO42 | GRCh38.p7 | 1:16252447 | CTCAGGTGTGATATG[C/T]GTTCCAAAACACACA | 54455 |
rs752719836 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16266462 | ACTCTGTGCAGACTC[A/G]CTTTCTCAGAGTGGG | 54455 |
rs752722120 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16252645 | ACCCATGAATCAACT[C/G]AGTGGTTTTGACACT | 54455 |
rs752738719 | in-del | -/CC | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16333437 | GGGCAAATAGTGAGA[-/CC]CCCCCCCCCCATTTC | 54455 |
rs752777134 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16265615 | AATGCATAATGCTTA[C/T]ACTGAGCTAGACACT | 54455 |
rs752825127 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16278184 | CAACATGGAGAAACT[C/G]CATCTCAACTAAAAA | 54455 |
rs752847793 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16312182 | TAGGTAACAGCAAGA[G/T]CCTGTCTCTATAAAC | 54455 |
rs752852612 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16324811 | ACACAGCAAGACTCC[A/G]TTTCAAAAAATCAAA | 54455 |
rs752857638 | in-del | -/AGAAAGAG | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16313367 | GAAAGAAAGAAAGAA[-/AGAAAGAG]AAAAGAAAGAAAACC | 54455 |
rs752860020 | in-del | -/CC | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16333438 | GCAAATAGTGAGACC[-/CC]CCCCCCCCCCATTTC | 54455 |
rs752883237 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16274643 | TGTTGCCAGGCTAGA[A/G]TGCAGTGGCGTGAAC | 54455 |
rs752906166 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16323453 | AAAAAGTAATTAAGG[A/G]AACTTCTTACCGATA | 54455 |
rs752938314 | snp | C/T | 1.68912e-05 | 0.00290608 | intron-variant | FBXO42 | GRCh38.p7 | 1:16294734 | GTAGAGTTTCCATGC[C/T]AAGGGAGTCACCTGG | 54455 |
rs753011506 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16249825 | AGAAGAAAAAAGCAG[C/G]CTGTAAGTGAATGGA | 54455 |
rs753026187 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16305479 | CCCAGCACTCTGGGA[A/G]GCCAAGGCAGGCCTA | 54455 |
rs753080936 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16304499 | TGTGTTTGCTGAACA[C/T]GTATTATGTTAAATA | 54455 |
rs753095371 | snp | A/G | | | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16317750 | GCAACAAAGTGAGAC[A/G]CCATCTCTACAAAAA | 54455 |
rs753099414 | in-del | -/GAG | | | cds-indel, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16248214 | GGCTTCAGGAGGCCT[-/GAG]GAGACAATCACCTTC | 54455 |
rs753122519 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16270577 | GGTGCAGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 54455 |
rs753132174 | snp | C/T | | | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16316844 | TGAATCATTAAGAGA[C/T]CCAGGCAGTAAAAAA | 54455 |
rs753207487 | snp | C/G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16350545 | CAGCCTGGGCAACAT[C/G/T]GGTGAAACCCCGTCT | 54455 |
rs753222867 | in-del | -/A | 1.68083e-05 | 0.00289894 | intron-variant | FBXO42 | GRCh38.p7 | 1:16315163 | CTTTCTCCTATCCAC[-/A]AGTACCTTTGATAAG | 54455 |
rs753245827 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16259490 | TACCTCTTGCCAGGC[A/G]CAGTGGCTCACACCT | 54455 |
rs753311800 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16269768 | AATCTCAGGTGATCC[A/G]CCTACCTCGGCCTCC | 54455 |
rs753337516 | snp | C/G/T | 3.39976e-05 | 0.00412284 | intron-variant | FBXO42 | GRCh38.p7 | 1:16253598 | AACTGAAAGACGCTA[C/G/T]AGTGTTTGCTGAATA | 54455 |
rs753358906 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16306803 | TCCCAGGCTCAAGCA[A/G]TACTCCTACCTCTGC | 54455 |
rs753371516 | in-del | -/TACTT | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16294104 | AAAAATCTAGCAGAA[-/TACTT]TATACTCAGTGGACA | 54455 |
rs753371609 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16255842 | GTAAAAAGACAGGAG[A/G]AAGTCAAGAAGTCAG | 54455 |
rs753372302 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16332145 | GATACAGCATATGTT[G/T]TGTTCATTCTGGGAT | 54455 |
rs753408701 | snp | C/T | | | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16354139 | ATTACAGGCGCCCGC[C/T]ACCGTGCCCAGCTAA | 54455 |
rs753423716 | snp | C/G | 1.65075e-05 | 0.00287289 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251035 | GGATGGGCACTGTTT[C/G]TCCACTGCTCAAACT | 54455 |
rs753443107 | in-del | -/AAAC | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16310975 | CCGGACTCCATCTCA[-/AAAC]AAACAAACAAACAAA | 54455 |
rs753611657 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16286054 | ACGCCCAGCTAATTT[C/T]TTTTTTAATTTTTTG | 54455 |
rs753629631 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16252446 | ACTCAGGTGTGATAT[A/G]CGTTCCAAAACACAC | 54455 |
rs753631317 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16273994 | AACGTGTTCAAAGAA[A/C]GAAGCCAGACATAAA | 54455 |
rs753634945 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16320494 | ATTTATTAACTTTCA[C/T]ATATATTTTTTGTTT | 54455 |
rs753649747 | snp | C/G | 1.64866e-05 | 0.00287106 | missense, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16305906 | GAAACCATGATAACA[C/G]TGATGGGCTACACCT | 54455 |
rs753662079 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16311657 | TCAGGGAAATGCAAA[G/T]TAAAATGAGATACCA | 54455 |
rs753663973 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16298698 | TATTTTTAGTAGATA[C/T]GGGGTTCCACTATGT | 54455 |
rs753703217 | snp | G/T | 1.6557e-05 | 0.00287719 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251114 | TGCAGAGGCCGAGGG[G/T]CCTTTGGAGGACATC | 54455 |
rs753711284 | in-del | -/AAAAAAAAAAA | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16341611 | AGACTGCGTCTTTTA[-/AAAAAAAAAAA]AAAAAAAAAAAAAGT | 54455 |
rs753718353 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16345507 | AAGACCCTGTAGCAA[C/T]GAGCATCCCTAGCAC | 54455 |
rs753720665 | snp | A/C | 1.67214e-05 | 0.00289144 | intron-variant | FBXO42 | GRCh38.p7 | 1:16294941 | AAAATACACAAATAA[A/C]TGCTGTGAAAATTCT | 54455 |
rs753748240 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16348112 | GTCATATCCTTGTAC[A/G]TGTAGCAAGCTGTCA | 54455 |
rs753817506 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16311758 | GAACTCTCATTCACT[A/G]CTAGTGGGAGTACAA | 54455 |
rs753831788 | in-del | -/AAAC | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16347523 | CCTCTCAAAACAAAC[-/AAAC]AAACAAACAAACAAA | 54455 |
rs753867649 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16277996 | GCAGTAAACCATGTT[C/T]GTGCCACTGTACTCC | 54455 |
rs753901393 | in-del | CCATACATTAAC/GTCTGCCAATTTCTGTTTTTTTTTTT | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16263796 | ACAAAAAACCCACGG[lengthTooLong]TTTTTTTTTTTTTTT | 54455 |
rs753931172 | in-del | -/AGC | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16260826 | TACCTCAGCCTCCTA[-/AGC]AGCTAGGACTACAGT | 54455 |
rs753934193 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16302544 | AAACGGAGTCTCGCT[C/T]TGTTGCCCAGGCTGT | 54455 |
rs753936609 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16303862 | GCCATTCTCCTGCTT[C/T]AGCCTCCCCAGTAGC | 54455 |
rs753945815 | in-del | -/GTT | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16334694 | AAAGATAATACCAAG[-/GTT]GTTATGAGTTATCTA | 54455 |
rs753990568 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16322235 | TGAGAGTCTGCTGCC[A/G]GAGAGGAAACTATTT | 54455 |
rs754048849 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16257791 | GTTCAAGTGATTTTC[C/T]TGCCTTAGCCTCCTG | 54455 |
rs754071513 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16248934 | TGGCTAAGGGAAAGG[A/G]TTCAGCATGATGTAA | 54455 |
rs754090461 | in-del | -/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16292147 | GTATGTTTTGTCAAA[-/G]GGAATATTCCAAATG | 54455 |
rs754100220 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16256343 | TCTTCAACTGGCTCA[C/T]TCATTTTTCTTGAAA | 54455 |
rs754102965 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16269468 | GTTCAAGCCATTCTC[A/G]TGCCTCAGCTTCCTG | 54455 |
rs754156394 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16283697 | ACACGGGATTTCACT[A/G]TCTTGACCAGGCTGG | 54455 |
rs754173671 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16283345 | TGAAAGGGAGGAAAC[C/T]GCAAAGAAAAAGAAA | 54455 |
rs754221535 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16246929 | TGACAGATTTAAATA[C/T]CAATGAAATCCATGT | 54455 |
rs754243679 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16268229 | AACAGAAAAATCCTT[C/G]TCAGCCCTGAGAGTG | 54455 |
rs754280178 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16311840 | GCTCTTACCATATGA[C/T]CCAGCAATTGTGCAT | 54455 |
rs754284117 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16327934 | TCAAACTCCTGACCT[C/T]AAGTGATCCGCCCAC | 54455 |
rs754309828 | snp | A/T | 4.96463e-05 | 0.00498203 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251435 | TGGAGTACTTGGAGA[A/T]ATGGCCTGTACAGGA | 54455 |
rs754395148 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16314574 | AAAGCTATGTTCACA[C/T]TGGCTATTACTATTA | 54455 |
rs754414084 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16261193 | GAAGTAAATTAAACA[C/G]AAGGCTATTCTTAGA | 54455 |
rs754437639 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16281973 | CCAAAGTGCTGGGAT[C/T]ACAGGTGTGAGCCAC | 54455 |
rs754451289 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16297242 | AGCCAATGCGCCCAG[C/G]CCCCCACCTTCTTTT | 54455 |
rs754517135 | snp | A/G | 1.65097e-05 | 0.00287308 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251039 | GGGCACTGTTTCTCC[A/G]CTGCTCAAACTCTGG | 54455 |
rs754521316 | in-del | -/AGAAAGAAA | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16350760 | AAAAAAAAAAAAAAA[-/AGAAAGAAA]GAAAGAAAGAAAGAA | 54455 |
rs754539255 | snp | C/T | 1.6715e-05 | 0.00289089 | intron-variant | FBXO42 | GRCh38.p7 | 1:16253735 | ACATCATTGCTCCTG[C/T]GAATTAAGGACAGAA | 54455 |
rs754550859 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16291760 | CACTGTAGCCTTGAA[A/C]TCCTGGGCTCAAGCA | 54455 |
rs754584549 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16292896 | TCTTCTATATTTTAG[A/G]ATCCATAACTCAGCT | 54455 |
rs754645215 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16319177 | GGAAGGAAACGAAGA[A/G]TAATCTCGAAATATA | 54455 |
rs754695096 | in-del | -/TGTGTA/TGTGTGTC | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16326048 | GTGTGTGTGTGTGTG[-/TGTGTA/TGTGTGTC]TCTGTGTGTGTCTGT | 54455 |
rs754711294 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16294292 | TAGTGGGACTGGGTA[A/G]GAATGTACCTACTGT | 54455 |
rs754718347 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16271777 | CTAGATGGAGAACCT[C/T]TTAGGATTAGGAACT | 54455 |
rs754753250 | snp | A/G | 3.34012e-05 | 0.0040865 | intron-variant | FBXO42 | GRCh38.p7 | 1:16252448 | TCAGGTGTGATATGC[A/G]TTCCAAAACACACAC | 54455 |
rs754808026 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16286072 | TTTTAATTTTTTGAG[A/G]AGATGGCCAGGCTGG | 54455 |
rs754811871 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16299843 | AGAGATGGAGTTTCA[A/C]CATGTTGGCCAGGAT | 54455 |
rs754813560 | snp | A/G | 1.64887e-05 | 0.00287125 | missense, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16305911 | CATGATAACACTGAT[A/G]GGCTACACCTAAGAC | 54455 |
rs754855340 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16345510 | ACCCTGTAGCAATGA[A/G]CATCCCTAGCACACA | 54455 |
rs754865102 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16298725 | ATGTTGGCCAGGCTG[C/G]TCTCGAATTCCTGAC | 54455 |
rs754872834 | in-del | -/AAATGA | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16324127 | TCATTTTATCAACTC[-/AAATGA]AAATGAAAAAGTTAT | 54455 |
rs754885171 | snp | A/G | 4.96611e-05 | 0.00498278 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251186 | GACGGCCCCTGCAAG[A/G]GCACTGGCCACGTGA | 54455 |
rs754926225 | snp | A/C | 1.64868e-05 | 0.00287109 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251721 | GATGGGCGAGAGTTC[A/C]AACTGGGGCTGAGTG | 54455 |
rs754930947 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16329852 | TACTCGGGAGGCTGA[G/T]GCAGGAGAATTACTT | 54455 |
rs754954162 | in-del | -/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16340104 | GGCGTGAACCCGGGA[-/T]TGCGGAGCTTGCAAT | 54455 |
rs755029570 | in-del | -/AC | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16252457 | TATGCGTTCCAAAAC[-/AC]ACACACACACAGAGT | 54455 |
rs755048090 | in-del | -/AGAA | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16313299 | AAAGAAGAAAGAGAG[-/AGAA]AGAAAGAAAGAGAAA | 54455 |
rs755054324 | in-del | -/AAAC | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16310978 | ACTCCATCTCAAAAC[-/AAAC]AAACAAACAAACAAA | 54455 |
rs755104158 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16264424 | GTTTTATACTCATTA[A/G]GACATTTCCTGGCCT | 54455 |
rs755132236 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16322303 | CTATACTAGGCCAGG[A/C]GTGATGGCTCACACC | 54455 |
rs755171335 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16303953 | AGACGGGGTTTCACC[A/G]TGTTAGCCAAGATGG | 54455 |
rs755171781 | snp | A/G | 1.64757e-05 | 0.00287012 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250715 | GTTTGTTTTTGGATA[A/G]TACTTCACATTCTGT | 54455 |
rs755228851 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16336790 | GGAGTTCAAGACCAG[C/T]CTGGCAAACATGGTG | 54455 |
rs755229696 | snp | C/G | 2.04853e-05 | 0.00320035 | intron-variant | FBXO42 | GRCh38.p7 | 1:16255860 | GTCAAGAAGTCAGCA[C/G]CACACACTTTATGTA | 54455 |
rs755241786 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16290366 | TTAGATGAGGTCATG[A/C]GGGTAGCCCTCATAA | 54455 |
rs755298032 | snp | C/G | 1.64768e-05 | 0.00287021 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251339 | TATGGATCCTAATCT[C/G]AGATCTTTCTGATCT | 54455 |
rs755312949 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16302562 | TTGCCCAGGCTGTAG[G/T]GCAGTGGTGCAATCT | 54455 |
rs755335307 | snp | A/C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16334388 | CAGTGAGCGGAGATC[A/C/G]AGCCTGGGCGACAGA | 54455 |
rs755352780 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16280234 | AACTCCAGTCTAACC[-/A]TAAGATAAACATCCA | 54455 |
rs755353895 | snp | C/G | 1.65086e-05 | 0.00287298 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251227 | GCACACCATTTGTCT[C/G]TTCAGGAGGGTGTCT | 54455 |
rs755458818 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16316000 | ACATGGAGAAACCCC[A/G]TCTCTACTAAAAATT | 54455 |
rs755495527 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16327974 | CCAAAGTGCTGGGAT[G/T]ACGTGTGTGACCCAC | 54455 |
rs755500292 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16283897 | CAGTTTTAATTTAAA[C/T]GTAAAATTTCTACTT | 54455 |
rs755514606 | in-del | -/A | 5.26477e-05 | 0.00513041 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250630 | ACACTGGAAAATTCC[-/A]AATTAAAAGCCACAG | 54455 |
rs755529733 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16283412 | TGGGAAAATCAACTG[C/T]GCTCCAGTACCAGTT | 54455 |
rs755531655 | in-del | -/AGC | 1.65359e-05 | 0.00287536 | intron-variant | FBXO42 | GRCh38.p7 | 1:16256798 | GTTAGCATTCAGGAT[-/AGC]CTCACAACAATCCGT | 54455 |
rs755534554 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16349340 | GCTCCCCAGCCATAC[C/T]ATATGCAACTTCAGA | 54455 |
rs755574710 | snp | A/G | | | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16352554 | GGATGGCGAGGGGCG[A/G]CCAGGGGGCGGCGCA | 54455 |
rs755640931 | snp | G/T | 8.24029e-05 | 0.00641831 | missense, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16315350 | TTGATCCATTGTCCC[G/T]TCCAGCACAGTTTCT | 54455 |
rs755661026 | snp | A/G | 1.70038e-05 | 0.00291575 | intron-variant | FBXO42 | GRCh38.p7 | 1:16253070 | TAGTAGCATGCACAT[A/G]GGAATGCCACAGAAG | 54455 |
rs755676713 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16258231 | GGTTGAGAAGGTAGA[A/G]CAGAGGACTGTCTTT | 54455 |
rs755678090 | snp | A/G | 1.70554e-05 | 0.00292017 | intron-variant | FBXO42 | GRCh38.p7 | 1:16253594 | TCCTAACTGAAAGAC[A/G]CTACAGTGTTTGCTG | 54455 |
rs755708006 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16304651 | ATAACACCTTGACCA[C/G]TCTGGAGTAGAGAAA | 54455 |
rs755721940 | snp | C/T | 1.64776e-05 | 0.00287028 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250914 | TTGCAGTTCATACTC[C/T]GGTATAGGGGTTTGC | 54455 |
rs755731485 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16284339 | CATCTACCCACTCAC[C/T]AGCACCTGCAATCAC | 54455 |
rs755777475 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16298666 | AGGCGCCCACCACCA[C/T]GCCCAGCTAGTTTTT | 54455 |
rs755809161 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16330681 | GTGCGGTGGCTCACG[C/T]CTGTAATCTCAGCAC | 54455 |
rs755833426 | snp | A/C/T | 6.59863e-05 | 0.00574364 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251009 | ATCTCCTTGGGCAGG[A/C/T]CCTGGGCGAGGGATG | 54455 |
rs755863230 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16329686 | TGGGTGCGGTGGCTT[A/G]TGCCTGTAAACCCAG | 54455 |
rs755877255 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16287289 | ACTTCTTGTACCCAT[C/T]AAGTCCTTGTTCTAA | 54455 |
rs755927847 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16297573 | CTCTACTAAGAAGTC[A/C]AGTCCAGGCCGGGCG | 54455 |
rs755955920 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16249391 | TGAGGTCAGCCATGC[A/G]TCAAGAAGTCAAGTA | 54455 |
rs755989623 | snp | C/G | 1.65814e-05 | 0.00287931 | intron-variant | FBXO42 | GRCh38.p7 | 1:16294773 | CAAAGATCAGCATTT[C/G]ATCTCTTACCTGAAG | 54455 |
rs756009419 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16262613 | AAGAATCGCTTGAAC[C/T]TGGGAGGTGGAGGTT | 54455 |
rs756037639 | in-del | -/GAA | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16313365 | AGAAAGAAAGAAAGA[-/GAA]AAGAAAGAGAAAAGA | 54455 |
rs756082689 | snp | C/T | 3.33084e-05 | 0.00408082 | intron-variant | FBXO42 | GRCh38.p7 | 1:16294930 | CACCTAGAAAGAAAA[C/T]ACACAAATAACTGCT | 54455 |
rs756119777 | snp | A/C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16341801 | CATGGAGAAAACCCC[A/C/G]TCTCTACTAAAAATA | 54455 |
rs756122802 | in-del | -/AAAA | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16338355 | ATGGCCCTATCTCCA[-/AAAA]AAAAAAAAAAAAAAA | 54455 |
rs756138652 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16345481 | ACTACTGAAAGGACC[C/T]AGAAACAATGAAGAC | 54455 |
rs756222101 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16331676 | GGATTTTCACTTGAA[A/C]TAGGGAGGCGGAGGT | 54455 |
rs756242427 | snp | A/G | 1.65427e-05 | 0.00287595 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251579 | AGGAGTCTGCCTTTG[A/G]GCCCTGGGTCTCAGT | 54455 |
rs756252425 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16275876 | GGCGTGGTGGTGGTA[C/T]GTGCTTGTAATCCCA | 54455 |
rs756270105 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16255418 | TGGCTCACTGCAATC[A/G]CCACTTCCCAGGTTC | 54455 |
rs756277917 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16333989 | TAAAAATAATAATCC[A/G]TCAGAAACTTCAAAA | 54455 |
rs756288039 | in-del | -/AAAAAAAAAAAAAAAA | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16259766 | CAAGACTCTGTCTCA[-/AAAAAAAAAAAAAAAA]AAAAAAAAAAAAAAG | 54455 |
rs756305685 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16290034 | AAGCTCCATGAGGGC[A/G]GGGGCCACAAAAGCA | 54455 |
rs756335461 | snp | C/T | | | downstream-variant-500B | FBXO42 | GRCh38.p7 | 1:16246781 | TGCTGGGATTACAAG[C/T]GTGAGCCACTGCGCC | 54455 |
rs756358594 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16288385 | CAATGAGCCCAGATC[A/G]CACCACTGCACTCCA | 54455 |
rs756367017 | in-del | -/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16253287 | TAACCTCTCCATTCT[-/C]CTAAAAACATATCAA | 54455 |
rs756468478 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16268124 | TGCAGTTCTAATGGG[A/G]GTGGGGGGCATAGGG | 54455 |
rs756510348 | in-del | -/CTC | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16281069 | CAGATTCAAGCAATT[-/CTC]CTCCTGCCTCAGCCT | 54455 |
rs756521900 | snp | A/C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16267071 | AACACTTCAAAATTC[A/C/T]TGAGTATAAAGTCTG | 54455 |
rs756541836 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16280197 | GGCATTATATCTCCA[C/T]GGTCTTCTTCCCAAA | 54455 |
rs756555214 | snp | C/T | 8.28645e-05 | 0.00643625 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251151 | ATGGCTTCCAGACTC[C/T]GACGCAGGGCACCTG | 54455 |
rs756559718 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16315003 | TTCAGTATTCAAGCT[A/G]TTCATTAAACTAACC | 54455 |
rs756592886 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16294153 | CACCAACCCCTCCAA[C/T]CTATGCCTCCTCAAA | 54455 |
rs756642583 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16339992 | ACCATCCTGGCTAAC[A/G]CAGTGAAACCCTGTC | 54455 |
rs756642922 | snp | A/G | 1.65425e-05 | 0.00287593 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251203 | CACTGGCCACGTGAG[A/G]TGGGGTATGCACACC | 54455 |
rs756710574 | in-del | -/GGGTGG/GT | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16326015 | TCAGTGCCCAAATTT[-/GGGTGG/GT]GTGTGTGTGTGTGTG | 54455 |
rs756830908 | snp | C/T | | | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16316944 | GCAAAGAACCACAGG[C/T]TATATACATATAAAT | 54455 |
rs756842334 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16266898 | CATATAACTTTGAAG[C/G]AAACAGATTCCTTAA | 54455 |
rs756863773 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16284132 | AATCTGATTAAGAAT[C/T]AAGGTGTTACCTTCA | 54455 |
rs756864521 | snp | A/G | 3.29935e-05 | 0.00406149 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16252349 | TTTTCTACCTTGAGT[A/G]GCTGCCAGGCCCAAG | 54455 |
rs756875163 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16325596 | CCCTTAATAAAACAG[-/A]AAAAAATTTAAAAAT | 54455 |
rs756905875 | in-del | -/TCTTT | | | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16247557 | TCCTCCTCCTCCTCC[-/TCTTT]TCTTTATTTTAAAGA | 54455 |
rs756908142 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16328131 | CACAACCCACATTTG[A/T]CAAAACCCACAGCAT | 54455 |
rs756915198 | in-del | -/GAAA | | | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16247449 | CCAGAATGACAAGGT[-/GAAA]GAAAGGAAAGGGAAA | 54455 |
rs756980644 | snp | A/G | 4.94173e-05 | 0.00497053 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250784 | CCTGCCTTGTACCAC[A/G]GTATGCAGGCTGGTT | 54455 |
rs756998648 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16341448 | CTACTGAAAATGCAA[A/C]AATTATTTGGGAGTG | 54455 |
rs757028074 | snp | C/G | 1.7063e-05 | 0.00292082 | intron-variant | FBXO42 | GRCh38.p7 | 1:16253060 | TTTGAACACTTAGTA[C/G]CATGCACATGGGAAT | 54455 |
rs757044515 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16247849 | ATAAGAGAACAGGAA[A/G]CTCTGTCCAAGAGGG | 54455 |
rs757056183 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16308418 | AGCCCAGGAGTTCGA[A/G]GCTGTAGTGCACAAT | 54455 |
rs757057332 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16340125 | AGCTTGCAATGAGCC[A/G]TGATCGTGCCACTGC | 54455 |
rs757143131 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16342104 | CAACATGGCAAAACC[C/T]TAACTCTACAGGCCA | 54455 |
rs757143697 | snp | G/T | 1.64754e-05 | 0.00287009 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250894 | GCACGTACATCTGCA[G/T]GGGCTTGCAGTTCAT | 54455 |
rs757144903 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16296006 | TTGATTAGATGATTG[C/T]ATACACATCACCAGG | 54455 |
rs757222100 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16333828 | AGATGGGTAGTGTTA[C/T]GGCTGAAAACTGTTA | 54455 |
rs757273012 | snp | G/T | 1.67094e-05 | 0.0028904 | intron-variant | FBXO42 | GRCh38.p7 | 1:16294756 | GTCACCTGGTAAGGA[G/T]GCAAAGATCAGCATT | 54455 |
rs757294665 | in-del | -/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16346771 | TTTTTTTTTTTTTTT[-/C]TGAGACAGAGTCTCA | 54455 |
rs757303378 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16253855 | TTCACTTTCACAGAC[C/T]GTGTGGGCTGGAGCA | 54455 |
rs757305045 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16348847 | TAATCAACATTGTAA[A/G]GAATAACAATTAAAT | 54455 |
rs757343662 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16287384 | ACTTTCCATCCTCTA[A/G]CATACTGTTATATAT | 54455 |
rs757359573 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16266854 | ATCATAATCAGAAAA[C/T]CTAGAGGGCACTGGA | 54455 |
rs757456312 | snp | A/C | 1.65463e-05 | 0.00287626 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251570 | GGAACCTGAAGGAGT[A/C]TGCCTTTGAGCCCTG | 54455 |
rs757472071 | in-del | -/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16337783 | CAGCTACTCGGGAGG[-/C]TGAGGCAGAAGAATT | 54455 |
rs757478023 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16301340 | ATACCAAATTTATTA[C/G]ATATCAACTATGAAC | 54455 |
rs757527281 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16300216 | GCTCACAGTACAGTA[C/T]GAATACTGGGCTAAC | 54455 |
rs757577643 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16325017 | CCAAAACAGGCAGAT[G/T]GCTTGAGCCCAGGAG | 54455 |
rs757582364 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16313460 | CAGTCCCTTACCTGT[A/G]GTTTTCCTCCCTTTA | 54455 |
rs757608496 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16279665 | ATTCAATGGAACATC[A/G]AGAACCAAGGGCAAT | 54455 |
rs757632514 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16265871 | CTGCATACTACACAG[G/T]TGGCTCTGAGTACAG | 54455 |
rs757644814 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16308263 | TGGAATTACAGGCGT[C/G]AGCCACTGTGTCCAG | 54455 |
rs757655763 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16278485 | AGACTACTGTCTTTT[C/T]TATTTTTATTTTGTT | 54455 |
rs757658037 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16334418 | GTGAGACTCCGCCTC[-/A]AAAAAAAAAAAAAAA | 54455 |
rs757671118 | in-del | -/TCTC | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16254509 | ACTCCTGGATGGCAG[-/TCTC]TCTTTCATGGTCACT | 54455 |
rs757710920 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16292661 | ATATTACAGGGAGAA[A/G]TAAGCACAGTAGTTG | 54455 |
rs757727294 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16335495 | TAGCTGGTTTCCCAC[C/T]TCCTTCCTTCTTCCT | 54455 |
rs757746794 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16336893 | GGGAGGCTGAGGCAG[C/G]AGAATCACTTGAACC | 54455 |
rs757788425 | in-del | -/TGAGA | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16348973 | CACCACTTAGTAATC[-/TGAGA]TATTTTAATTGCAGC | 54455 |
rs757799210 | snp | C/T | 1.72832e-05 | 0.00293961 | intron-variant | FBXO42 | GRCh38.p7 | 1:16253764 | AAGGATAAAGGTAGT[C/T]AGGAGCTCCCAGGGA | 54455 |
rs757815046 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16338161 | CTACTCGGGAGGCTG[A/G]GGCAGGAGAATGGTG | 54455 |
rs757835469 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16326591 | CAGGAGGCCGAAGTG[A/G]GAGGATCACTTGAGC | 54455 |
rs757863245 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16343784 | GCCCAGATCGTGCCA[C/T]TGTACTTCAGCCTGG | 54455 |
rs757949448 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16247834 | TGTATAACCTGTGAA[A/G]TAAGAGAACAGGAAG | 54455 |
rs757960749 | snp | C/T | 3.31066e-05 | 0.00406844 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251134 | TGGAGGACATCGCTT[C/T]GATGGCTTCCAGACT | 54455 |
rs757980621 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16261371 | AAGGGCTTTCCAAAA[C/T]GACGTCTCAGATATC | 54455 |
rs758024274 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16295704 | GGCCAATAAATGAAT[C/T]TTTATATGACACACA | 54455 |
rs758048712 | snp | A/G | 1.65501e-05 | 0.00287659 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251193 | CCTGCAAGGGCACTG[A/G]CCACGTGAGGTGGGG | 54455 |
rs758079088 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16294382 | TCCCCAAATATCTGA[A/G]CTGGCAACAACAACA | 54455 |
rs758117159 | in-del | -/AGAGAGAAAGAA | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16313294 | AAGAAAAGAAGAAAG[-/AGAGAGAAAGAA]AGAGAGAAAGAAAGA | 54455 |
rs758134944 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16295689 | TGAGCCACCATGCCC[A/G]GCCAATAAATGAATC | 54455 |
rs758176756 | snp | G/T | 1.64749e-05 | 0.00287005 | missense, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16315215 | AAGGGCCGCAGTTTT[G/T]TGTTCCTGATACGGT | 54455 |
rs758190288 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16319244 | AAGTGACAGACCGGG[A/G]AGAGCAGAGAACAGA | 54455 |
rs758219133 | snp | A/G | 1.6486e-05 | 0.00287102 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16252318 | GCACCACAGTTCTGG[A/G]GCCCCATGCTCTTCA | 54455 |
rs758229928 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16273439 | GGAGAGCTCTCTGGG[A/G]TGCTTGCTATGTCTA | 54455 |
rs758247035 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16350748 | TGAGAAACTGCAAAA[-/A]AAAAAAAAAAAAGAA | 54455 |
rs758301421 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16322131 | ACCTTTATATGTTAC[C/T]AGATGTTGTCAAAAT | 54455 |
rs758355341 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16253566 | CTTACCTGACTCCCT[A/C]CTCCCTCTCCCGTCC | 54455 |
rs758414693 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16345964 | CAAAAAATAAGGAAG[C/T]ACTCCAAGACCAAAG | 54455 |
rs758421477 | snp | A/G | 1.64795e-05 | 0.00287045 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16256727 | CCTTGTACACGACCA[A/G]AGTTGCTCCAGCTTT | 54455 |
rs758458589 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16265689 | CAAATTCCATGTTCT[A/G]AGTAATCAAGAAATC | 54455 |
rs758476823 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16298847 | CTTAACTAGTGTCCA[C/T]TATAACATTGCTTAA | 54455 |
rs758604250 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16312967 | GCCTCACTAATTTTT[C/G]TATTTTTAGTAGAGA | 54455 |
rs758655346 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16304273 | TGGCATGTGCCACCA[C/T]GGCTGGTTAATTTTT | 54455 |
rs758675685 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16312190 | AGCAAGATCCTGTCT[C/T]TATAAACATTTTTTT | 54455 |
rs758719231 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16336859 | GTGTGGTGGCAAACG[C/T]CCGTAATTCTAGCTA | 54455 |
rs758741092 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16308042 | CTTCAAGACTTACTA[C/T]AAAAGCTACAGTAAT | 54455 |
rs758766797 | snp | A/G | | | missense, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16256667 | CTGGCTGGTGTAGGG[A/G]ATAAGGGCTTGGCCG | 54455 |
rs758782831 | in-del | -/TTGCT | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16286848 | GAAGAGTCATCTTGA[-/TTGCT]TTCTTTCTCTTTCCT | 54455 |
rs758807015 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16335305 | CCATCAAGACCAGCT[A/G]ATTTTTTTATTTTGT | 54455 |
rs758866480 | snp | A/G | 3.3972e-05 | 0.00412127 | intron-variant | FBXO42 | GRCh38.p7 | 1:16253076 | CATGCACATGGGAAT[A/G]CCACAGAAGCAATAC | 54455 |
rs758877715 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16304559 | ACTACTCCCTAAGCA[A/G]AATCTTAGAAATACC | 54455 |
rs758882125 | in-del | -/CCTCCAATA | 1.6477e-05 | 0.00287024 | cds-indel, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16315306 | GTCTAGTCTCCTCAG[-/CCTCCAATA]CCTCCAATACTGGGT | 54455 |
rs758898435 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16332531 | ACAATGTTTCAACTA[A/C]TGAATTTCTTTTCCT | 54455 |
rs758923872 | snp | C/T | | | utr-variant-5-prime | FBXO42 | GRCh38.p7 | 1:16352436 | CCACTCAAACGCCGC[C/T]GCCGCCGCAGCTGCT | 54455 |
rs758956530 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16336167 | GATCTTGAACTCCTG[A/T]CCTCAGGTGACCTGC | 54455 |
rs758966253 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16297628 | GCACTTTGGGAGGCC[A/G]AGGCAGGCAGATCAT | 54455 |
rs758991004 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16274474 | TCTTGATCTAGGTAA[C/T]GATCACATGACTGTA | 54455 |
rs759082244 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16275355 | AGGTGCGATGGCTCA[C/T]GTCTGTAATCTCGGT | 54455 |
rs759145391 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16302093 | AGACAGATGGTAATA[A/T]ATAATGGAGGAAGGT | 54455 |
rs759162675 | in-del | -/AAAAA | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16350744 | AGAGTGAGAAACTGC[-/AAAAA]AAAAAAAAAAAAGAA | 54455 |
rs759171531 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16320777 | ATGTTAGCCAGGCTG[G/T]TCTCAAACTCCCGAC | 54455 |
rs759217140 | snp | A/G | 1.70942e-05 | 0.00292349 | intron-variant | FBXO42 | GRCh38.p7 | 1:16255703 | TGGAGCAAACCAAAT[A/G]TACTTACATTTGCCG | 54455 |
rs759323491 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16254623 | AGCTCCTATAATCTC[C/T]CTCCATAACTGTTTT | 54455 |
rs759339601 | snp | A/G | | | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16353855 | ACCAGGCCTATTGAT[A/G]ATAACTATTTCAACT | 54455 |
rs759346511 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16253433 | CACAGCAAAGTAAAT[A/G]CTTTGGGGAGGAGCA | 54455 |
rs759346551 | snp | C/T | 3.31055e-05 | 0.00406837 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251188 | CGGCCCCTGCAAGGG[C/T]ACTGGCCACGTGAGG | 54455 |
rs759374568 | snp | A/G | 1.65405e-05 | 0.00287576 | intron-variant | FBXO42 | GRCh38.p7 | 1:16256587 | TTCCAGATTTAAAGA[A/G]TTTATCTTTGTGACT | 54455 |
rs759402433 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16324544 | AGGTAGAAGCCAAGT[A/G]TGGTGACTCATGCCT | 54455 |
rs759425178 | in-del | -/TAC | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16341100 | ATGATCTCCAAAATA[-/TAC]TACTAGGTGAAAAGA | 54455 |
rs759429592 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16335063 | AAACCTCGTCTGTAC[-/A]AAAAAAAAAAAAAAA | 54455 |
rs759463754 | in-del | -/AAAACC | 1.65985e-05 | 0.00288079 | intron-variant | FBXO42 | GRCh38.p7 | 1:16252416 | ATAGCTGTAAGAGAA[-/AAAACC]AATAACAAGACTCAG | 54455 |
rs759511474 | in-del | -/GTGTGTGTGT | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16271259 | TGCGTGTGTGTGTTG[-/GTGTGTGTGT]GTGTGTGTGTGTGTG | 54455 |
rs759530857 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16320299 | TGGAGAGGTGGAAGT[C/T]GCAGTAAGCCGAGAT | 54455 |
rs759539554 | snp | C/T | | | downstream-variant-500B | FBXO42 | GRCh38.p7 | 1:16246657 | TACAGGTGCCTGCCA[C/T]CATGCCCGGCTAATT | 54455 |
rs759589233 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16310320 | GAGCTGAGACTGCGC[C/T]ACTGAACTCCAGCCT | 54455 |
rs759620917 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16257968 | TTACAGGCGTGAGCC[A/C]CCATGCCTCGCTGAG | 54455 |
rs759638815 | snp | A/G | 1.64781e-05 | 0.00287033 | missense, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16315315 | TCCTCAGCCTCCAAT[A/G]CTGGGTGGGGCTCCT | 54455 |
rs759666723 | snp | A/C/G | 4.95032e-05 | 0.00497489 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16252290 | GCTCCCTGCTTACCC[A/C/G]GCAAGCTGGATGGCA | 54455 |
rs759695860 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16258926 | AAATTTTTTTGTTGT[A/G]ATCAGGTCTTGCTAT | 54455 |
rs759697448 | in-del | -/TGA | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16337250 | ACTGTATTCTCACCT[-/TGA]TGATGCCAGCACTGC | 54455 |
rs759772081 | snp | C/T | 1.64743e-05 | 0.00287 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250873 | CCTTGGTGTCTTTAA[C/T]GTCCAGCACGTACAT | 54455 |
rs759776844 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16253924 | GAACCAGAAAGAGAC[C/T]ATGTTGCTGAATCCC | 54455 |
rs759809225 | snp | A/G | | | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16353620 | ATGAGTTCTTGGTTC[A/G]CTGCAACCTCTGTCT | 54455 |
rs759812765 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16270472 | ATTCCCAAGGGAAGA[C/T]TGGGGATGAATTCAT | 54455 |
rs759865601 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16352121 | AGTCACCCTGCCCAA[C/G]CAGGACCGACCCCCG | 54455 |
rs759871884 | snp | C/T | 1.64882e-05 | 0.00287121 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250989 | ATGGGAGGTAAGGAA[C/T]GTCCATCTCCTTGGG | 54455 |
rs759872444 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16330150 | CAGAAAGTAATTTCA[C/T]TCCTGCATACCTTGG | 54455 |
rs759891103 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16286489 | ATGAGAACAGCATGG[A/G]CGAACCACCCCCATG | 54455 |
rs759970141 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16286670 | CTCCCCTGAACTCCA[A/T]ATACATATATCTCCA | 54455 |
rs759987264 | snp | A/G | 1.64792e-05 | 0.00287042 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16294814 | GATCCACTCTTTGCT[A/G]TTTAGGTCAAGTCTC | 54455 |
rs760039067 | snp | C/T | 1.65507e-05 | 0.00287664 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251437 | GAGTACTTGGAGATA[C/T]GGCCTGTACAGGACT | 54455 |
rs760070779 | snp | C/T | 3.31186e-05 | 0.00406918 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251553 | GAAAGGCTCCCTTCC[C/T]GGGAACCTGAAGGAG | 54455 |
rs760076460 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16298190 | GAGATTGCGCCACTG[C/T]ACCCCAGCCTGGGCG | 54455 |
rs760100172 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16310685 | TATATAGAATATCCA[A/G]AGAACTCTTAAAACT | 54455 |
rs760101539 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16272555 | TGAGCCACCGTGCCC[A/G]GTGGGTCACTGCAAC | 54455 |
rs760108299 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16343259 | GGATTTAGAAGAACT[A/G]CAGGCTAGGCGCAGT | 54455 |
rs760139275 | snp | A/G | | | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16316665 | GCTTGAACCTGGGAG[A/G]CAGAGGTTGCAGTGA | 54455 |
rs760149441 | snp | A/G | | | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250714 | CGTTTGTTTTTGGAT[A/G]GTACTTCACATTCTG | 54455 |
rs760156280 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16287101 | AGAAAGCCACACATA[C/T]GTGATACATCCCTTT | 54455 |
rs760228929 | snp | A/C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16287802 | CAGTGTCAAACTCTC[A/C/G]GCCAGGCACAGTGGC | 54455 |
rs760230710 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16300647 | TTGATAAGGTCTCTA[A/G]TTACGTAACTATGAA | 54455 |
rs760265441 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16273735 | AATACAAAAATTAAC[C/T]GGGTGTGGTGATGCA | 54455 |
rs760281526 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16299730 | GCTCACTGCAACCTC[C/T]GCCTCCTGGGTTCAA | 54455 |
rs760303561 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16266324 | AAGAGCCATGCTAAA[A/G]TAAGTTTGCTAACAG | 54455 |
rs760329669 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16332119 | ATTAGCTTTAATAGT[C/T]AGTCACTTCTGATAC | 54455 |
rs760334919 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16312541 | TAAACAGGGAGAGTA[C/T]ACAGGATTTTTAGGG | 54455 |
rs760376893 | in-del | -/CC | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16287516 | TACCAGGGGGGCAAT[-/CC]ATGAATATTTGTTAC | 54455 |
rs760438245 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16345410 | CCTGGGTGATGGAGC[A/G]AGACTCTGTCTTAAA | 54455 |
rs760492886 | snp | C/T | 1.66067e-05 | 0.00288151 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16253723 | TCAAGGACCCAGACA[C/T]CATTGCTCCTGTGAA | 54455 |
rs760498031 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16323279 | AAAAATTAGCTGGGC[A/G]TGGTGGTGGGCACCT | 54455 |
rs760503409 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16291311 | CATGATAGCATACAG[-/A]AAACATTGTCTTAGG | 54455 |
rs760530903 | snp | A/G | 1.65578e-05 | 0.00287726 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251109 | AGTGCTGCAGAGGCC[A/G]AGGGGCCTTTGGAGG | 54455 |
rs760547423 | snp | A/G | 1.65616e-05 | 0.00287759 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251174 | GGCACCTGGGGAGAC[A/G]GCCCCTGCAAGGGCA | 54455 |
rs760570925 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16277936 | AGTCCCAGCTACTAG[C/G]GAGGCTGAGGCAGGA | 54455 |
rs760574486 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16324414 | CAGAACATTATATAA[C/T]AAATGACCTATGAGA | 54455 |
rs760624004 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16292172 | CAAATGCTCTATTTT[C/T]AAAAATTCATATTCC | 54455 |
rs760629582 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16337256 | TTCTCACCTTGATGA[C/T]GCCAGCACTGCCAGT | 54455 |
rs760731427 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16288799 | TCCACCTCTACTAAA[C/T]ATACAAAAATTAGCC | 54455 |
rs760766107 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16270425 | GGCCTAACAACTGGA[C/T]GCTGAAGTACTTAGG | 54455 |
rs760767174 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16352042 | GGTGGGTTCGCTCCC[A/T]ACCCAAGGGCTGGCT | 54455 |
rs760820261 | snp | A/G | 6.58957e-05 | 0.00573964 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16305852 | ATAAGGATAGGTACG[A/G]CTCTCCCACTGAATG | 54455 |
rs760828497 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16291124 | CTTCCTGTACATACT[C/G]TGTTAGAAGACAACC | 54455 |
rs760838748 | snp | C/T | 1.6528e-05 | 0.00287467 | stop-gained, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16315185 | TTTGATAAGTCGATA[C/T]CACTGTTTGCAGACA | 54455 |
rs760871939 | in-del | -/TG | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16347142 | AAATACACTTATCTG[-/TG]TGTGTGTGTGTGCGC | 54455 |
rs760915887 | snp | A/G | 1.65061e-05 | 0.00287277 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250688 | TCTCTTTGCTCGTAC[A/G]AAGTACAAGGCGTTT | 54455 |
rs760926611 | snp | C/T | 1.65141e-05 | 0.00287346 | intron-variant | FBXO42 | GRCh38.p7 | 1:16252280 | TAGCCTGTCAGCTCC[C/T]TGCTTACCCGGCAAG | 54455 |
rs760946264 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16283605 | CGGGTTCAAGCAATT[A/C]CCTGCCTCAGCCTCC | 54455 |
rs760969409 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16350251 | GATTTAGCATAACAG[C/T]GCAACATATTATGCC | 54455 |
rs760978351 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16263318 | TGGGTGTGGTGGCAG[A/G]TGCCTTGTAGTCCCA | 54455 |
rs761035823 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16314185 | TCGAACTTGACCTCA[A/G]GTGACCCACCTGCCT | 54455 |
rs761039915 | in-del | -/AC | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16333436 | TGGGCAAATAGTGAG[-/AC]CCCCCCCCCCCATTT | 54455 |
rs761057076 | in-del | -/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16326701 | AAAAAAAAAAAAAAA[-/G]AAAAAAATTATTCTT | 54455 |
rs761088705 | snp | C/T | 4.9675e-05 | 0.00498348 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16252397 | AACAACCAAGCATCC[C/T]TGAATAGCTGTAAGA | 54455 |
rs761093387 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16342933 | ATTCACATGTCAACT[A/T]CCCCTTTGACCTTTC | 54455 |
rs761146519 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16340872 | GTGGCTTTAAGGTCA[C/T]ACAGCCAATGAGTAG | 54455 |
rs761187686 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16262001 | ACAGGCGTGAGCCAC[C/T]GCGCCTGGCCCAGGT | 54455 |
rs761199756 | snp | A/G | 4.94287e-05 | 0.00497111 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16256695 | CCGCGTCCAGCCACC[A/G]AACAGCACTAGCAAG | 54455 |
rs761202514 | snp | A/C | 1.65416e-05 | 0.00287586 | intron-variant | FBXO42 | GRCh38.p7 | 1:16256799 | GTTAGCATTCAGGAT[A/C]TCACAACAATCCGTA | 54455 |
rs761257671 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16265037 | TATTTGATAACAAGA[C/T]AAAACAATCACCTGT | 54455 |
rs761266242 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16321651 | GAGTGTAAGGTTTAT[C/T]GACATGTCTACTCAG | 54455 |
rs761267950 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16298459 | AAAAGCACATTCTTC[A/T]CCTCTTGATATTCCA | 54455 |
rs761294337 | snp | C/G | 3.30748e-05 | 0.00406649 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251427 | GGAGCAGATGGAGTA[C/G]TTGGAGATATGGCCT | 54455 |
rs761296984 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16264900 | GGCATTCTTGTTTAC[A/G]TTTGCAAAGAAGCTG | 54455 |
rs761316851 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16277800 | AATCCCAGCACTTTC[A/G]GAGGATGAGGCAGGA | 54455 |
rs761321193 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16310818 | TCACTTGACATCAGG[A/C]GTTCAAGACCAGCCT | 54455 |
rs761340222 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16344834 | CCGGGCGTGGTGGCT[C/G]ACACCTGTTATCCCA | 54455 |
rs761393513 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16303653 | ACTCACTGCAACCTC[A/C]GCCTCCCGGGTTCAA | 54455 |
rs761393673 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16264168 | GTAATGACTTTGAAG[A/C]ACTGCCCGAATGTGC | 54455 |
rs761450488 | in-del | -/GTGA | 1.64836e-05 | 0.0028708 | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16256619 | ACCAATTTTTAGAGG[-/GTGA]GTAAGTGTGTATTTC | 54455 |
rs761546617 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16343470 | ACAGTAACTTGAGCC[C/T]GGGAGGGAGAGGTTG | 54455 |
rs761599198 | snp | C/T | 3.30006e-05 | 0.00406192 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251016 | TGGGCAGGCCCTGGG[C/T]GAGGGATGGGCACTG | 54455 |
rs761613292 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16289735 | AGTAGGTCTCCCCTA[A/G]CAGCATGGGCAACAT | 54455 |
rs761649890 | snp | A/G | 1.6884e-05 | 0.00290547 | intron-variant | FBXO42 | GRCh38.p7 | 1:16315456 | ATAGGTAAAACATAA[A/G]TATCAGTATTCCACT | 54455 |
rs761663487 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16336525 | ATCACGCCTGGCTAA[C/G]TTTTGTATTTTTAGG | 54455 |
rs761667959 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16276796 | CTCCATGGGGGAACC[C/T]AAGAGTAAACAAAAA | 54455 |
rs761701231 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16331483 | AAACCGGCTTGGTGC[A/G]GTGGCTCATGCCTGT | 54455 |
rs761711450 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16256214 | CTGTCATTAAGAGAT[A/G]TATGTTTGAAAAACA | 54455 |
rs761719192 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16290980 | ACATGTAAAAAGACA[A/T]CTGATGCAGCAGTAT | 54455 |
rs761770422 | in-del | -/TG | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16304484 | AGTCCATTTAAATTT[-/TG]TGTTTGCTGAACATG | 54455 |
rs761853370 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16269223 | CTCCTAAGTAGCTGG[G/T]ACTACAGGCACATGA | 54455 |
rs761860986 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16248513 | ACTAAGGGAAAGACT[G/T]TAAGGTTGAGATTCT | 54455 |
rs761895309 | snp | G/T | 1.64732e-05 | 0.0028699 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16305825 | GAAGCGCTGAGTGAT[G/T]GGGGTTCCAGGATAA | 54455 |
rs761960269 | snp | A/T | 1.64942e-05 | 0.00287173 | missense, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16294893 | AACACATACATAGAC[A/T]GATTAGCATCATAAT | 54455 |
rs762051071 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16315709 | TAAACCAGAAAACTT[A/G]TTCTCCAACAATTCT | 54455 |
rs762064643 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16327602 | TCAATTCTTTAAAGC[A/G]TTTTAAAATCCAAGT | 54455 |
rs762071424 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16295468 | TGATCTCGGCTCACT[A/G]CAACATCTGCCTCCC | 54455 |
rs762119109 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16340640 | CTACTGAGGGTTAGG[A/G]TTTTGCCATGCCAAG | 54455 |
rs762124476 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16308005 | AGGAGGAGAACAAAG[A/T]CAGAAGATTGATACC | 54455 |
rs762170608 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16340215 | AAATTAAAAATCACC[C/T]AGCAGGTAGATTTCC | 54455 |
rs762190420 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16248465 | AAGTGGAAGGAATCA[A/G]CACGTTAACAGCTGG | 54455 |
rs762225778 | in-del | -/TC | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16327003 | ATCTCTCTCTCACCA[-/TC]TCTCTCTATGACCCA | 54455 |
rs762245478 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16261824 | TTCTCCTGCCTCAAC[A/C]TCCTGAGTAGCTGGG | 54455 |
rs762261229 | in-del | -/CAAA | | | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16317605 | TCTCAAACAAGCAAA[-/CAAA]CAAACAAACAAACAA | 54455 |
rs762298377 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16260747 | GGCACCCAGGCTGGA[A/G]TGCAGTGGTGTGACT | 54455 |
rs762299136 | snp | C/T | 1.65655e-05 | 0.00287793 | intron-variant | FBXO42 | GRCh38.p7 | 1:16252239 | AAGTAATGTGGTTTT[C/T]CACAATTTAGGACCT | 54455 |
rs762325471 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16274192 | GCATCTGCAATCCCA[A/G]CTACTTGGGAGGCTG | 54455 |
rs762327499 | in-del | -/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16304116 | AGCCAAATTTGTATT[-/T]TTTTTTTTTTTTTTT | 54455 |
rs762333802 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16306686 | ATAATTAGTTTACAA[C/T]TGATTATGTTTTGTT | 54455 |
rs762349510 | in-del | -/CTTT | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16293929 | TCTTAGTCCAGTGCC[-/CTTT]CTAATATACAATGAT | 54455 |
rs762363970 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16327626 | TCCAAGTAACACAGA[A/C]AAGTGACCATCCTAA | 54455 |
rs762369925 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16320515 | TTTTTTGTTTTATTA[C/T]TTTTTTGAGATAGGG | 54455 |
rs762436643 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16303467 | TTCTTACAGATTTCC[A/G]AATGTCAGAGGAGGA | 54455 |
rs762443124 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16290880 | TAAGCTACCCAGTCT[A/G]TGGTATTTTGTATGG | 54455 |
rs762466352 | in-del | -/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16286616 | TATTACTAACTAATA[-/G]GCTAATGAGCCCTAC | 54455 |
rs762469480 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16276670 | GATATACAAGGATAA[A/G]GCATCATATGAAATG | 54455 |
rs762472064 | in-del | -/AAA | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16313365 | AAGAAAGAAAGAAAG[-/AAA]GAAAGAGAAAAGAAA | 54455 |
rs762486019 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16321986 | CCAGCCTAGCCAACA[C/T]GGCGAAACCCTGTCT | 54455 |
rs762538143 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16315027 | ACTAACCAGGGTAAG[-/A]AAGAAAACCGGGTAG | 54455 |
rs762540949 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16331370 | CAGTGAGCCGAGATC[A/G]TGCCACTGCACTCCA | 54455 |
rs762551598 | in-del | -/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16301684 | TCAAAAAAAAAAAAA[-/C]AACAAAAAAAAAAGA | 54455 |
rs762641326 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16296269 | AAAATAAAATAAAAT[A/T]AAATTAAGTAAACAA | 54455 |
rs762677064 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16320949 | CCCTTGCACAACATT[C/T]TGACAGACTATAAGC | 54455 |
rs762737107 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16267708 | GTTACTGATTGACAT[A/C]AACATTCACTGGTAT | 54455 |
rs762744159 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16329124 | GCTGAGATTGTGCCA[A/C]TGCACTCCAGCCTGG | 54455 |
rs762779149 | in-del | -/AC | 1.70043e-05 | 0.0029158 | intron-variant | FBXO42 | GRCh38.p7 | 1:16253597 | TAACTGAAAGACGCT[-/AC]AGTGTTTGCTGAATA | 54455 |
rs762791662 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16289197 | GCTAGGAGTTGAAGA[C/T]CAGCCCAGGCAACAT | 54455 |
rs762830105 | snp | C/T | 1.67699e-05 | 0.00289563 | intron-variant | FBXO42 | GRCh38.p7 | 1:16315442 | ACTCAACAGCTGTAA[C/T]AGGTAAAACATAAAT | 54455 |
rs762843304 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16302271 | GGGCAGGCCGGGTGC[A/G]GTAGCTCAACGCCTG | 54455 |
rs762852667 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16348761 | AGCGGTCAGCTTCAA[C/T]CAAAAAGGAATTAAG | 54455 |
rs762876803 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16254934 | ATTTGTTTTTTTCTT[G/T]TCTTTCCTTCTTTCT | 54455 |
rs762935698 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16281040 | GATTCTCAGCTCACC[A/G]CAACCTCTGCCTCCC | 54455 |
rs763001187 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16327011 | CTCACCATCTCTCTC[C/T]ATGACCCACTTCTAA | 54455 |
rs763020046 | snp | A/G | 1.65425e-05 | 0.00287593 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251088 | GAAGACCCAAGAGGA[A/G]GACTTAGTGCTGCAG | 54455 |
rs763058120 | snp | C/G | 2.15613e-05 | 0.00328332 | intron-variant, splice-acceptor-variant | FBXO42 | GRCh38.p7 | 1:16253182 | ACATTGAAAATAAAC[C/G]TACAAAGACACAGGT | 54455 |
rs763063776 | in-del | -/TTT | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16283494 | TCTAACTGTGGCAAG[-/TTT]TTTTTTTTTTTTTTT | 54455 |
rs763080564 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16266629 | TTGTTTTGTTTTGTG[A/G]TAGTGAGGAGCCTCA | 54455 |
rs763082399 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16310723 | ATTAGGGCCAGGCGC[A/G]GTGGCTCACGTCTGT | 54455 |
rs763171361 | snp | A/G | | | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16353691 | ACTGGGACTACAGGC[A/G]GGCACCACCATGCCT | 54455 |
rs763205946 | snp | C/T | 1.64765e-05 | 0.00287019 | missense, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16294857 | AAAGCAGCATTGCAG[C/T]TGCTCTGGGTACAGC | 54455 |
rs763270634 | snp | A/C | | | intron-variant, utr-variant-5-prime | FBXO42 | GRCh38.p7 | 1:16261102 | AAGTCTGATGCCTTA[A/C]AAGGTCTAGTGTTTC | 54455 |
rs763282596 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16339943 | GGGTGATAAAGCAAG[A/C]CCCTGTCTCAAGAAA | 54455 |
rs763339261 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16331779 | AATGCAGCCAGGCGC[A/G]GTGGCTCATGCCTGT | 54455 |
rs763371397 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16305485 | ACTCTGGGAGGCCAA[G/T]GCAGGCCTATTGCTT | 54455 |
rs763382921 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16274016 | AGACATAAAATACTA[C/G]CTATCACAGACGTCC | 54455 |
rs763393594 | snp | C/T | 9.89022e-05 | 0.00703145 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251655 | ACTGGAGACTGAGAG[C/T]GGTACTCTCGGGTTT | 54455 |
rs763483821 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16286886 | CTACATCCAAAATAT[G/T]AGCAAATCCCTTTGG | 54455 |
rs763488264 | snp | A/T | | | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16317768 | ATCTCTACAAAAAAA[A/T]AATTAACCGGGTGTG | 54455 |
rs763504059 | snp | A/G/T | | | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16352865 | GTGCTTGAGGTGTGC[A/G/T]GGAGAAGTCTTCCCT | 54455 |
rs763517716 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16253276 | TCTAGTTACCATAAC[A/C]TCTCCATTCTCCTAA | 54455 |
rs763519740 | in-del | -/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16348010 | AAAAAAAAAAAAAAA[-/G]AAAAAAAGAAAAGAA | 54455 |
rs763541579 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16330284 | CCAGCACTTTGAGAC[A/G]CCAAGATGAGAGGAT | 54455 |
rs763594734 | snp | A/G | 3.29538e-05 | 0.00405904 | missense, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16256682 | GATAAGGGCTTGGCC[A/G]CGTCCAGCCACCAAA | 54455 |
rs763626388 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16297360 | TAATGAAAGCAGTAT[A/G]TTTAGTGCCTTAAAC | 54455 |
rs763670156 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16341318 | CTATAAAAGTGGTAG[G/T]AGGCTGGAAGCCGTG | 54455 |
rs763690223 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16308366 | GTGTATGCCTGTGGT[C/T]CTAGCTACATGAGAA | 54455 |
rs763709610 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16276706 | TATTGTGGTAATAAA[A/T]CATGAAGTACTGTTA | 54455 |
rs763717509 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16262308 | GACTACAGGAGTATA[C/T]CAAAATGCCTGGCTC | 54455 |
rs763722354 | snp | C/T | 1.64781e-05 | 0.00287033 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251322 | AGATCCCAATTCAGA[C/T]CTATGGATCCTAATC | 54455 |
rs763731314 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16249058 | AAACGCTAATAATAA[A/T]AAGAGGAGTGTCAGG | 54455 |
rs763733544 | in-del | -/CA | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16273826 | GAGGCTGCAGTGAGC[-/CA]CAAGATTGTGCCACT | 54455 |
rs763761537 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16321108 | TACAATAGCAAGCCA[A/C]CATAAAGAGACTCAT | 54455 |
rs763764834 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16275501 | GTTCATGCCTGTAGT[A/C]CTTGCTACTTGGGAG | 54455 |
rs763803507 | snp | C/G | 3.29478e-05 | 0.00405867 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16315233 | TTCCTGATACGGTGA[C/G]AGAAAGGACAGGATA | 54455 |
rs763820093 | snp | A/C/G/T | 6.59213e-05 | 0.00574085 | synonymous-codon, missense, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16315329 | TACTGGGTGGGGCTC[A/C/G/T]TCATCTTGATCCATT | 54455 |
rs763840092 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16335365 | CTGGTCTCAAACTCC[A/T]GGGTTCAAGTGATCC | 54455 |
rs763858540 | in-del | -/A | 1.79942e-05 | 0.00299946 | intron-variant | FBXO42 | GRCh38.p7 | 1:16255829 | AGTTCCACCTAATGT[-/A]AAAAGACAGGAGGAA | 54455 |
rs763873257 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16266348 | CTAACAGCTAGGCAC[-/A]GTGGCATGTACCTGT | 54455 |
rs763905895 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16298246 | ACAAAAACAAAAACA[A/C]CAAAGAACTACAAAT | 54455 |
rs763942405 | in-del | -/TAATCA | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16300309 | GTTTACGACACATAC[-/TAATCA]TAATCATCCCTATTA | 54455 |
rs763981751 | snp | C/T | 1.67184e-05 | 0.00289118 | intron-variant | FBXO42 | GRCh38.p7 | 1:16252451 | GGTGTGATATGCGTT[C/T]CAAAACACACACACA | 54455 |
rs764040868 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16255004 | CACATTTGGAGGGCC[C/T]ACCATTTCCACTTGT | 54455 |
rs764087511 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16348769 | GCTTCAATCAAAAAG[G/T]AATTAAGATCTTCTC | 54455 |
rs764088056 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16288078 | TTGAACCCAGGAGAT[A/G]GAGTGAGCCGAGATC | 54455 |
rs764088721 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16282695 | ATTTTTAAAAATGCT[G/T]ATCGGCTGAGTGCAG | 54455 |
rs764134572 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16266662 | CTGGCGTGTGTATGG[C/G]GGGTGGGAAGGATGG | 54455 |
rs764135682 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16253591 | CCGTCCTAACTGAAA[A/G]ACGCTACAGTGTTTG | 54455 |
rs764174405 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16315648 | TTTGATTACATTTTT[C/T]CTCTTCACTGAAAAC | 54455 |
rs764177660 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16247072 | GGGTGTGCACTGACA[C/T]GAACCCTGGTTGGAG | 54455 |
rs764321240 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16293808 | CCCATTTAAAAATAG[C/T]CATTTAGTACTACTC | 54455 |
rs764472890 | snp | A/G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16325000 | CCCAACACTTTGAGA[A/G/T]GCCAAAACAGGCAGA | 54455 |
rs764483981 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16291193 | TCTACCTACCTCGAT[A/G]CACTAAAATGAGTGA | 54455 |
rs764543177 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16286954 | ACTTTACTCCAAGTG[C/T]CTATCATTTTCAGCC | 54455 |
rs764557096 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16337821 | CCCAGGAGGCAGAGG[A/T]TGCAGTGAGTGGAGA | 54455 |
rs764570421 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16305500 | GGCAGGCCTATTGCT[A/T]GAGCTCAGTTCAAGA | 54455 |
rs764615930 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16259144 | GGCTGTTGTCTTTCA[C/T]ATAGCCTTACTGTTC | 54455 |
rs764659425 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16319055 | CCCAGACCATTTACT[A/G]TGCCACCCCACTTTA | 54455 |
rs764724513 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16270864 | ACTAAAACAGACAAA[A/T]AGCCCTCAGCCCCAG | 54455 |
rs764740038 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16298001 | GAGGCTGAGGCGGGT[C/G]GATCACTTGAGGTCA | 54455 |
rs764775550 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16308247 | CAGCCTCTCAAAGTG[C/T]TGGAATTACAGGCGT | 54455 |
rs764781543 | snp | A/G | 3.39963e-05 | 0.00412274 | intron-variant | FBXO42 | GRCh38.p7 | 1:16253751 | GAATTAAGGACAGAA[A/G]GATAAAGGTAGTTAG | 54455 |
rs764782795 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16275367 | TCATGTCTGTAATCT[C/T]GGTACTTCGAGAGGC | 54455 |
rs764831757 | snp | A/G | 1.65537e-05 | 0.0028769 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251127 | GGGCCTTTGGAGGAC[A/G]TCGCTTTGATGGCTT | 54455 |
rs764847727 | snp | C/T | 4.96553e-05 | 0.00498249 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251190 | GCCCCTGCAAGGGCA[C/T]TGGCCACGTGAGGTG | 54455 |
rs764860277 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16261236 | CTACAAGGCTCTGGG[A/C]CACACTCCACCTCTA | 54455 |
rs764871818 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16300835 | AAAAGGACATTCTAC[A/G]TTAATTAAAGCTTGC | 54455 |
rs764889498 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16288018 | GGGTGTGGTGGTGGG[C/T]GCCTGTAATCTCAGC | 54455 |
rs764900478 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16332252 | CATACACTGAGAGCT[C/T]TGCTTGCACTTAAAA | 54455 |
rs764935727 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16320873 | CACCAAGGAAAAGAG[C/T]CCAAAGAAATGGATT | 54455 |
rs764956704 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16287224 | CTCTGGGTCTTTGCA[C/T]TGATTATTCTCTGTT | 54455 |
rs764976183 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16348669 | TTGCGCCACTGCACT[C/T]CAGCCTAGGCGATAG | 54455 |
rs764998079 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16254740 | CAGGGGGAATGACCA[C/T]AACTGCTGCTACCGC | 54455 |
rs765025330 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16346563 | CGTGGTGGTGGGCGC[A/G]TGTAGTCCCAGCTAC | 54455 |
rs765028964 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16319191 | AGTAATCTCGAAATA[C/T]ACTTTGGGGCTTTGA | 54455 |
rs765146240 | snp | C/T | 1.64784e-05 | 0.00287035 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16315317 | CTCAGCCTCCAATAC[C/T]GGGTGGGGCTCCTCA | 54455 |
rs765189676 | snp | A/G | 1.64779e-05 | 0.00287031 | missense, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16315207 | TTGCAGACAAGGGCC[A/G]CAGTTTTGTGTTCCT | 54455 |
rs765241672 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16266411 | GGATGGCTTAACCTC[C/T]TGCCTTAAGATAGGT | 54455 |
rs765271717 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16312777 | AGGGTAGGGGATATA[C/T]GAGAAATCGGTTTTG | 54455 |
rs765298469 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16265591 | AGATGAATAATGGTA[A/G]GTGAAGCTAATGCAT | 54455 |
rs765299964 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16293420 | GCCAGTGGGCCTGGC[C/T]TGTAGGTTTGTTTTT | 54455 |
rs765337715 | snp | C/T | 1.64743e-05 | 0.00287 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250719 | GTTTTTGGATAGTAC[C/T]TCACATTCTGTTTCT | 54455 |
rs765351689 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16304158 | TTTCACTCTTGTTGC[C/T]CAGGCTGGAGTGCAA | 54455 |
rs765355755 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16324717 | AGCTACAGGGGGTCT[C/G]AGGTGCGAGCATCGC | 54455 |
rs765409092 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16323439 | AAACAAACAAACAAA[A/C]AAAGTAATTAAGGGA | 54455 |
rs765409158 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16337620 | AGGCACAGTGGCTCA[C/T]GCCTGTAATCCTAGC | 54455 |
rs765433001 | snp | A/C/T | 3.29491e-05 | 0.00405877 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250876 | TGGTGTCTTTAATGT[A/C/T]CAGCACGTACATCTG | 54455 |
rs765433660 | snp | C/G | | | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16353630 | GGTTCGCTGCAACCT[C/G]TGTCTTTCAGGCTCA | 54455 |
rs765469000 | in-del | -/AAAC | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16346203 | GAAAAGCAAAAAAGT[-/AAAC]AAACACCCTACCTTA | 54455 |
rs765505330 | in-del | -/AAAAAAAATAT | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16311496 | TGTCTCAAAAAAAAA[-/AAAAAAAATAT]AAAAAAAATATATAT | 54455 |
rs765526508 | snp | C/T | 1.69143e-05 | 0.00290807 | intron-variant | FBXO42 | GRCh38.p7 | 1:16294725 | AATGATCAGGTAGAG[C/T]TTCCATGCCAAGGGA | 54455 |
rs765540888 | snp | A/G | | | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16317656 | TGGGCAGGCACAGTG[A/G]CTCATGCCTATAATC | 54455 |
rs765556674 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16334989 | CCCAGCACTGTGGGA[A/T]GCCAAGGTGGGCGAA | 54455 |
rs765620567 | snp | C/T | 1.6476e-05 | 0.00287014 | missense, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16294839 | AGTCTCCAGAGGTCA[C/T]TGAAAGCAGCATTGC | 54455 |
rs765620616 | snp | C/G | 1.65534e-05 | 0.00287688 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251439 | GTACTTGGAGATATG[C/G]CCTGTACAGGACTGT | 54455 |
rs765620692 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16249781 | GGACTTCACCACATA[C/T]GAAAAAAAAAAAAGA | 54455 |
rs765630162 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16269726 | GACGGGGTTTCTCCA[C/T]GTTGGTCAGGCTGGT | 54455 |
rs765642023 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16330217 | TCATAATGGGGAAAT[G/T]AAGATTAAAAAATTT | 54455 |
rs765656237 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16290521 | ACATGGTGAAACTCC[A/G]TCTCTACTAAAAATA | 54455 |
rs765724686 | snp | C/T | | | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16316820 | AGGCAGTATTTACAA[C/T]AGAAAATATGAATCA | 54455 |
rs765860089 | in-del | -/AAGGGCC | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16324364 | ACAGATGGACCCACT[-/AAGGGCC]AAGGACACATAAATT | 54455 |
rs765884817 | in-del | GCGAGACTCCGTCTCAA/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16337869 | AGCCTGGGAGAAAGA[GCGAGACTCCGTCTCAA/T]AAAAAAAAAAAAAAA | 54455 |
rs765932105 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16321307 | ATGCCCAACACCAAT[A/T]TGCATAGCCCTTCTT | 54455 |
rs765973678 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16272679 | CACTTTGATCCCTAA[C/T]TACCTTTCCTATCCC | 54455 |
rs765992592 | snp | C/T | | | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16317948 | AAAGAAGAAGAAGAA[C/T]ATATACTATACGATT | 54455 |
rs766008457 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16253390 | TGAATGTCAACCACA[G/T]AAAATGCAGGATTCT | 54455 |
rs766018431 | snp | A/G | 0.000198649 | 0.00996419 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251111 | TGCTGCAGAGGCCGA[A/G]GGGCCTTTGGAGGAC | 54455 |
rs766019404 | snp | C/T | 8.51013e-05 | 0.00652253 | intron-variant | FBXO42 | GRCh38.p7 | 1:16253595 | CCTAACTGAAAGACG[C/T]TACAGTGTTTGCTGA | 54455 |
rs766048462 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251612 | TCCCCAGCGGCCGTT[-/A]ACACAAGGAGCTTCA | 54455 |
rs766051928 | snp | C/T | | | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16353580 | AGACAGGGTCTAACT[C/T]TGTTGCCCAGGCTGG | 54455 |
rs766055798 | in-del | -/AATT | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16348855 | ATTGTAAGGAATAAC[-/AATT]AAATATTTACTGTAT | 54455 |
rs766097467 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16312556 | TACAGGATTTTTAGG[A/G]CAGTGAAGCTATTAT | 54455 |
rs766111200 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16346464 | GAGTCCGAGGCGGGC[A/G]GATCATGAGGTCAGG | 54455 |
rs766153559 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16265310 | TGGTCAGGCTGGTCT[C/T]GAACTCCCAACCTCA | 54455 |
rs766221070 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16324484 | GGCTTCTAACTAGTA[C/T]AAGGAAGGTTCACAG | 54455 |
rs766316191 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16264349 | AAAAAGGCACATAAC[A/C]ACTATGGTGACATAT | 54455 |
rs766328602 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16303798 | TCACCGAGGCTAGAG[G/T]GCAGTGGCGTGATCT | 54455 |
rs766380720 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16336003 | ATGGCGCAATCTCGG[C/T]TCATTGCAACCTCAC | 54455 |
rs766387741 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16323333 | TGAGGCCAGAGAATC[A/G]CTTGAACCTGGGAGG | 54455 |
rs766390274 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16334419 | GTGAGACTCCGCCTC[-/A]AAAAAAAAAAAAAAA | 54455 |
rs766397343 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16277974 | TTGAGCCCAAGAGGT[C/T]GAGGCTGCAGTAAAC | 54455 |
rs766450246 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16322267 | TTTGGCCCAGTAGTA[A/T]CTTTTTCTTCCGAAA | 54455 |
rs766506643 | snp | C/T | 1.6513e-05 | 0.00287336 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16315188 | GATAAGTCGATACCA[C/T]TGTTTGCAGACAAGG | 54455 |
rs766513176 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16257787 | CTGGGTTCAAGTGAT[C/T]TTCCTGCCTTAGCCT | 54455 |
rs766515532 | in-del | -/TGTGTC/TGTGTGTGTGTC | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16326040 | GTGTGTGTGTGTGTG[-/TGTGTC/TGTGTGTGTGTC]TGTGTGTGTCTGTGT | 54455 |
rs766532786 | in-del | A/GAAAGAAGAAAAGAT | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16270707 | AAAAAGAAAAGAAAA[A/GAAAGAAGAAAAGAT]AAATTCCAAATCCCT | 54455 |
rs766540876 | in-del | -/AAAAAAAAAAA | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16341612 | AGACTGCGTCTTTTA[-/AAAAAAAAAAA]AAAAAAAAAAAAAGT | 54455 |
rs766594413 | snp | C/T | 3.30251e-05 | 0.00406343 | intron-variant | FBXO42 | GRCh38.p7 | 1:16252281 | AGCCTGTCAGCTCCC[C/T]GCTTACCCGGCAAGC | 54455 |
rs766608692 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16334515 | AAAGGCCAGTGATAT[G/T]GTCTATGTTAAACAG | 54455 |
rs766628169 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16342396 | GCGAAACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 54455 |
rs766638043 | in-del | -/TT | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16308496 | AGACCCATCTCTCTT[-/TT]TTTTTTTTTTTTTTT | 54455 |
rs766676617 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16314245 | GTGAGCCACCACACC[C/T]GGCCAAGAAACATAT | 54455 |
rs766678692 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16328892 | GGGATTGGCCGGGTG[C/T]GGTGGCTCACGCCTG | 54455 |
rs766726043 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16333436 | TGGGCAAATAGTGAG[-/A]CCCCCCCCCCCCATT | 54455 |
rs766727103 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16315937 | GCACTTTGGGAGACC[A/G]AGGCGGGCAGATCAC | 54455 |
rs766730059 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16342968 | CACACTGTGATACAG[A/C]TGGAAAGCCCTGCCA | 54455 |
rs766732216 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16327887 | TCGTATTTTAGTAGA[C/G]ACTGGGTTTCACCAT | 54455 |
rs766746982 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16248675 | TGGCCCAGCTTTCCC[G/T]TGTAAATAAGGACCC | 54455 |
rs766761082 | snp | C/T | 1.6477e-05 | 0.00287024 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16256704 | GCCACCAAACAGCAC[C/T]AGCAAGTCCTTGTAC | 54455 |
rs766767231 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16281956 | CAAGTGATCCTCGAC[C/T]CCCAAAGTGCTGGGA | 54455 |
rs766791919 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16343631 | GTTCAAGACCAGCCT[C/T]GCCAAGATGGTGAAA | 54455 |
rs766802120 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16262184 | TTCATATATATGTGT[A/G]TGTGTATATGTATAT | 54455 |
rs766826969 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16283686 | ATTTTTAGTAGACAC[A/G]GGATTTCACTATCTT | 54455 |
rs766842836 | snp | A/G | 4.94173e-05 | 0.00497053 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250849 | CTTTCCATTTGACCC[A/G]CCCCTTCTCCTTGGT | 54455 |
rs766916789 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16247706 | TAAAATGAAATTTAA[C/G]CTTGTTTCAACACCA | 54455 |
rs766961668 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16265178 | GGCTCACCGCAGCCT[C/T]TGCCTCCCAGTTTCA | 54455 |
rs766982363 | snp | C/T | 0.00011577 | 0.00760735 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251429 | AGCAGATGGAGTACT[C/T]GGAGATATGGCCTGT | 54455 |
rs767011648 | in-del | -/TC | 1.65061e-05 | 0.00287277 | intron-variant | FBXO42 | GRCh38.p7 | 1:16256774 | CTAGGGAAAGTCAGT[-/TC]AACACCATGGTTAGC | 54455 |
rs767018847 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16295688 | ATGAGCCACCATGCC[C/T]GGCCAATAAATGAAT | 54455 |
rs767050871 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16251991 | CATATGCTATCATTA[C/G]AGATATGTATACAGA | 54455 |
rs767103955 | snp | C/T | | | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250944 | CCAACATTTAGGGAC[C/T]GTGGAGGGTGGTGGC | 54455 |
rs767122291 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16269556 | TTGAGACAGAGTTTC[A/G]CTCTTGTTGCCCAGG | 54455 |
rs767127044 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16290683 | GGTGACAGAGTGACA[-/A]AAAAAAAAAAAGAAG | 54455 |
rs767146129 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16265070 | TAATTGGGGATGCCT[A/G]TATTTTATGCACGAT | 54455 |
rs767149463 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16345088 | TGAGAGACAGAGTGA[G/T]ACTCCGTCTCAAAAA | 54455 |
rs767167688 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16319611 | GGTTTCCTGAAAACT[C/G]TATTAGAAAAAGGAT | 54455 |
rs767170544 | snp | A/G | 6.59207e-05 | 0.00574073 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16315332 | TGGGTGGGGCTCCTC[A/G]TCTTGATCCATTGTC | 54455 |
rs767192799 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16298494 | TCCAGAAAAAGAAAT[C/T]AGCAATGTCCTATGA | 54455 |
rs767206288 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16310856 | ACAGTGAAACCCTGT[C/G]TCTGCTAAAAATACA | 54455 |
rs767222290 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16336639 | TGGGATTACAGGCAT[A/G]AGCCACTGTCCCTAG | 54455 |
rs767238972 | snp | C/G | 1.70956e-05 | 0.00292361 | intron-variant | FBXO42 | GRCh38.p7 | 1:16253585 | CCTCTCCCGTCCTAA[C/G]TGAAAGACGCTACAG | 54455 |
rs767277427 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16276823 | AAAACTGTCCAGATG[G/T]TAGGCAGACAGGATC | 54455 |
rs767287880 | in-del | -/CT | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16269107 | AGCCACCGCACCTGG[-/CT]TTTTTTTTTTTTGTG | 54455 |
rs767320463 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16303654 | CTCACTGCAACCTCC[A/G]CCTCCCGGGTTCAAG | 54455 |
rs767328940 | snp | C/T | 3.3129e-05 | 0.00406982 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16253715 | GCTCAAGGTCAAGGA[C/T]CCAGACATCATTGCT | 54455 |
rs767328992 | snp | A/G | 1.64996e-05 | 0.0028722 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251017 | GGGCAGGCCCTGGGC[A/G]AGGGATGGGCACTGT | 54455 |
rs767349649 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16343541 | ACAGAGCCAGACCCT[A/G]TGTCTAAAAAAATAA | 54455 |
rs767462596 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16275630 | TCTCTTACCCAAAAA[C/T]AGAAAAGGAAGAATA | 54455 |
rs767476901 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16331553 | TGAGCTCAGGGGTTC[A/G]AGACCAGCCTGGCCA | 54455 |
rs767490476 | snp | A/C | 1.65556e-05 | 0.00287707 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251107 | TTAGTGCTGCAGAGG[A/C]CGAGGGGCCTTTGGA | 54455 |
rs767501800 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16256215 | TGTCATTAAGAGATA[C/T]ATGTTTGAAAAACAA | 54455 |
rs767528735 | snp | C/T | 1.65479e-05 | 0.0028764 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251574 | CCTGAAGGAGTCTGC[C/T]TTTGAGCCCTGGGTC | 54455 |
rs767548696 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16335488 | AGAGAATTAGCTGGT[C/T]TCCCACTTCCTTCCT | 54455 |
rs767557343 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16255317 | TTAGAGCCATGCTCA[C/G]GAATACTGACCCTAA | 54455 |
rs767587012 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16303569 | AAGGCAAGAAGATAA[A/T]TTTTTTTTTTTTTTT | 54455 |
rs767587088 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16289955 | TATACTTCATTCCGT[C/T]TGTTTCCTTCATAAT | 54455 |
rs767702726 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16313797 | ATTGAGACAACCCTC[A/G]CTTGATAAAAAATGA | 54455 |
rs767707020 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16267898 | TGCCACAGGCATGAA[C/T]TAAAGGAAATTCTCT | 54455 |
rs767740267 | snp | G/T | 1.64735e-05 | 0.00286993 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16305831 | CTGAGTGATTGGGGT[G/T]CCAGGATAAGGATAG | 54455 |
rs767772661 | in-del | -/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16346755 | TACTGAACAGTACAT[-/T]TTTTTTTTTTTTTTT | 54455 |
rs767792609 | snp | C/T | 0.000115801 | 0.00760836 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250683 | CATTATCTCTTTGCT[C/T]GTACAAAGTACAAGG | 54455 |
rs767820468 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16314832 | GAGCTTGCAGTGAGC[C/T]GAGATTGCGCCACTG | 54455 |
rs767856491 | in-del | -/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16256377 | AATAAATCTCTTCTA[-/T]TTTTTTCTCTTTAGA | 54455 |
rs767865954 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16295547 | AGGTGTGCACCACCA[C/T]ACCCAGCTAATTTTT | 54455 |
rs767899446 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16343499 | TGTAGTAAGCAGAGA[C/T]TGCACCACTGCACTC | 54455 |
rs767907343 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16294049 | AAGACTGAGTCCTAA[C/T]ACTAAAAAGCCAAAT | 54455 |
rs767951869 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16311259 | AGGTGGTAAGATTGC[C/T]TGAGCCCAAGAGTTC | 54455 |
rs767958533 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16306761 | CTGCAGTGGCATGCA[C/T]GACTTTAGCTCACTG | 54455 |
rs768038091 | snp | A/G | 1.64817e-05 | 0.00287064 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250951 | TTAGGGACTGTGGAG[A/G]GTGGTGGCCCAGGCG | 54455 |
rs768062563 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16268959 | GACTACAGACACGCA[A/T]CACCACACCCAGTTA | 54455 |
rs768076976 | snp | A/G | 1.65217e-05 | 0.00287412 | intron-variant | FBXO42 | GRCh38.p7 | 1:16256788 | GTAACACCATGGTTA[A/G]CATTCAGGATCTCAC | 54455 |
rs768086377 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16260938 | TAAACTCCTGGCCTC[A/G]AGTGATTCTCCCACC | 54455 |
rs768102581 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16258899 | TGTAATACCATATCC[A/G]GCTAATTTTTAAAAT | 54455 |
rs768121826 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16277502 | GGCCGAGGCAAGCGG[A/G]TCACTTGAGCTCAGA | 54455 |
rs768172012 | in-del | -/AGAG | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16291907 | AAATTCCTGGCCTCA[-/AGAG]ATCCTCCTGTCTCAG | 54455 |
rs768173275 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16291820 | AGGACTACAGGCACA[A/T]GCCATCATGCCCGGC | 54455 |
rs768194272 | in-del | -/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16261846 | GTAGCTGGGACTACA[-/G]GCACCCCCCGCCATG | 54455 |
rs768271641 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16333356 | GGTGGCTTATGCCTA[C/T]AATCACAGCAACTCA | 54455 |
rs768293947 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16337034 | CTGTCTTTCCAAACA[C/G]AAGTGCACATATTTT | 54455 |
rs768305678 | in-del | -/TGTGTC/TGTGTGTA | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16326046 | GTGTGTGTGTGTGTG[-/TGTGTC/TGTGTGTA]TGTCTGTGTGTGTCT | 54455 |
rs768349560 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16336434 | CGTGATCTTGGCTCA[C/T]TGCAACCTCCACCTC | 54455 |
rs768371458 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16256162 | ACAGCTAACAAGCGC[C/T]ACGTACTAAGTCTTC | 54455 |
rs768456015 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16304936 | ATTGCACCACTGCAA[G/T]CCACCCTGGGCAACA | 54455 |
rs768466327 | snp | A/G | 1.65285e-05 | 0.00287471 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251418 | TATCCTTCAGGAGCA[A/G]ATGGAGTACTTGGAG | 54455 |
rs768473935 | snp | A/G | 0.00078918 | 0.0198486 | intron-variant | FBXO42 | GRCh38.p7 | 1:16315445 | CAACAGCTGTAATAG[A/G]TAAAACATAAATATC | 54455 |
rs768481206 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16257342 | CCAGGCCCCTAGCTA[C/T]GGGCTTCACATAACC | 54455 |
rs768492533 | in-del | -/AA | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16310193 | GCAAGACTCCATCTC[-/AA]AAAAAAAAAAAAAAA | 54455 |
rs768516362 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16328652 | ACATGTGTTAGTATA[C/T]ACTCATCTACCACCT | 54455 |
rs768538460 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16270183 | TATAAAGCCACCAGT[A/C]CCCACTCCCAGTCTA | 54455 |
rs768563937 | snp | C/T | 1.65581e-05 | 0.00287728 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251523 | AGGATAGGAGAGCCG[C/T]CTCCTCTGGCTGGGG | 54455 |
rs768588625 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16248191 | ACGTGAAGTCCCACC[A/G]CACAGGTGGCTTCAG | 54455 |
rs768614394 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16249557 | ATGAGTGTGCTCAAT[A/G]TGCTTTGGAAGTAAA | 54455 |
rs768720065 | snp | C/T | 1.65149e-05 | 0.00287353 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16253684 | CCAGAGATGTTCGGC[C/T]TGGACCACGCCCACT | 54455 |
rs768742297 | snp | A/G | 1.88149e-05 | 0.0030671 | intron-variant | FBXO42 | GRCh38.p7 | 1:16255665 | ACCTGTTATTCCCAG[A/G]AGTATTTACCTTCAG | 54455 |
rs768768294 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16284707 | GCGCAGGGACTCATG[A/C]CTGTAATTCCAGCAC | 54455 |
rs768796073 | snp | A/G | 1.65512e-05 | 0.00287669 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251097 | AGAGGAGGACTTAGT[A/G]CTGCAGAGGCCGAGG | 54455 |
rs768799876 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16313653 | CCCTCTAGGTGGACT[C/T]TGGGAGTTGACAAGG | 54455 |
rs768809280 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16327453 | GCTGAAAAACCAAAA[A/C]GTAAAACAAAACAAA | 54455 |
rs768832485 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16295416 | CTTTTTTTGAGATGG[A/C]GTCTCCCTCTGTCAG | 54455 |
rs768892100 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16309215 | TGGGATTACAGGCAC[A/G]CGCCACCATACCCAG | 54455 |
rs768972399 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16288557 | ACTAACCTCTCCCAA[A/G]TATTTATTTTCCACT | 54455 |
rs768972544 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16299937 | CGTGAGCCACCATGC[C/T]CGGCCACACTCAACT | 54455 |
rs768984176 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16264031 | GGCCAGGCTGGTCTC[A/G]AACTCCTGGCCTCAG | 54455 |
rs769015457 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16275136 | TAAATTCAATAGCAA[G/T]AAACATTCTGAGATT | 54455 |
rs769176769 | snp | A/G | 1.65037e-05 | 0.00287256 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16252363 | TGGCTGCCAGGCCCA[A/G]GGACCAGAATGCATG | 54455 |
rs769188288 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16287732 | TAGGATTACAGGTGT[A/G]AGCCACTGTGCCTGG | 54455 |
rs769237431 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16300587 | TATCCCATGCTTAAA[C/G]AGACTATGCTGTCAT | 54455 |
rs769249864 | snp | C/T | 1.71587e-05 | 0.002929 | intron-variant | FBXO42 | GRCh38.p7 | 1:16251808 | ACAAAGGACCAGTGC[C/T]CACACTCTTCTATGA | 54455 |
rs769281804 | snp | A/G | 3.38289e-05 | 0.00411258 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250663 | AAGGAAAGGGGTTTA[A/G]AACACATTATCTCTT | 54455 |
rs769300254 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16350894 | AGATTGAATCATCTA[C/T]TTATACTGGCTTGTC | 54455 |
rs769300320 | snp | A/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250829 | CACAGAACTGCTATT[A/T]AATACTTTCCATTTG | 54455 |
rs769336456 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16331784 | AGCCAGGCGCGGTGG[C/T]TCATGCCTGTAATCC | 54455 |
rs769338733 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16347774 | GCGGGCAGATCACGA[C/G]GTCTGGAAATCGAGA | 54455 |
rs769351496 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16290721 | GATGCCAGAGCTCAC[C/T]CTCTGCTACATGAAA | 54455 |
rs769473739 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16257139 | ATGAGCACCCCTTCC[C/T]ATCCCTTTAACAAAC | 54455 |
rs769489274 | in-del | -/TGTTT | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16269856 | TTGTTTTTTCTGTTT[-/TGTTT]TGTTTTGTTTTGTTT | 54455 |
rs769493715 | snp | C/T | 1.65029e-05 | 0.00287248 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251403 | CCTATTTTCAGGTCG[C/T]ATCCTTCAGGAGCAG | 54455 |
rs769507109 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16302126 | GAATAGTATATTAGG[A/G]AAGCAGAGAGGAAGA | 54455 |
rs769530631 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16284334 | CACTGCATCTACCCA[C/T]TCACCAGCACCTGCA | 54455 |
rs769534980 | snp | A/C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16256026 | GTTCTGAATGTAAAC[A/C/G]GTCTGGAGGGAGAGA | 54455 |
rs769580385 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16268783 | AGCCTGACCAACATG[C/G]AGAAACCCCGTCTCT | 54455 |
rs769592292 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16280801 | CAAAAGAAAAGAAGA[A/T]CGAAAACTACTCACA | 54455 |
rs769621255 | snp | G/T | 1.65031e-05 | 0.00287251 | intron-variant | FBXO42 | GRCh38.p7 | 1:16256602 | GTTTATCTTTGTGAC[G/T]TACCAATTTTTAGAG | 54455 |
rs769695192 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16282684 | ACCCCATTTCCATTT[A/T]TAAAAATGCTGATCG | 54455 |
rs769706951 | in-del | -/GTTTCACT | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16280987 | TGTTTTTGAGACAGA[-/GTTTCACT]GTTGTTGCCCAGGCT | 54455 |
rs769711077 | snp | A/G | 1.64849e-05 | 0.00287092 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16256746 | TGCTCCAGCTTTGGG[A/G]GAAGGATAGGACCCT | 54455 |
rs769724319 | snp | A/G | | | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16315313 | TCTCCTCAGCCTCCA[A/G]TACTGGGTGGGGCTC | 54455 |
rs769724525 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16282477 | GTGATCCACCCGCCT[C/T]GGCCTCCCAAAGTGC | 54455 |
rs769805824 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16307314 | GACCAGCCCGGGCAA[C/T]ATAGCAAGACCCCAT | 54455 |
rs769854608 | snp | A/G | | | downstream-variant-500B | FBXO42 | GRCh38.p7 | 1:16246767 | TCGGCCTCCCAAAGT[A/G]CTGGGATTACAAGCG | 54455 |
rs769855069 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16326849 | ATGGAGATGAGCTAC[A/C]TAAATGTCATCTAAG | 54455 |
rs769889781 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16325442 | AATAATTTGGCATAA[C/T]CATTGTTGCTATTAG | 54455 |
rs769918403 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16313091 | TGTTCCACTGTGTCC[A/G]CTCAGAGGAATTTGT | 54455 |
rs769950759 | snp | A/G | 8.26071e-05 | 0.00642625 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16253658 | GGCCACCTCGAGGAT[A/G]AGGACTGGGGCCAGA | 54455 |
rs769961856 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16260445 | AACTCCTGAGCTCAG[A/G]CAATCCACTGGCCTC | 54455 |
rs769988825 | in-del | -/TTT | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16304114 | CCAGCCAAATTTGTA[-/TTT]TTTTTTTTTTTTTTT | 54455 |
rs770027269 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16326772 | AGTCATCTAAAACAC[A/G]TAAGCCAGAATCAAC | 54455 |
rs770037325 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16275025 | GCCAGTAAGCAGAAA[C/T]ATCAGCAATCCATTA | 54455 |
rs770038031 | in-del | -/TGTGTA/TGTGTGTA | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16326032 | GTGTGTGTGTGTGTG[-/TGTGTA/TGTGTGTA]TGTGTGTGTGTGTGT | 54455 |
rs770045877 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16318845 | GCCACTCAGGGGAAT[C/G]TAGTACTGGGCAGAA | 54455 |
rs770059714 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16346157 | CCACTGAGGTGACCA[C/T]TTCACCAATTCTTTA | 54455 |
rs770069609 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16257531 | ACTTTAGAGATAACA[A/C]ATGTCTTACAGGAGC | 54455 |
rs770076018 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16323299 | GGTGGGCACCTGTAA[G/T]CCCAGCTACTCGGGA | 54455 |
rs770095185 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16332890 | ATTATCAGGCAATAG[A/T]GACCAAAGCATGTCA | 54455 |
rs770168198 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16313626 | AGCAGTTTCAATACA[A/G]CTGGTTCTTAGCCCT | 54455 |
rs770170311 | in-del | -/AACC | | | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16317627 | ACAAACAAACAAACA[-/AACC]GAAGACAGAAGAATG | 54455 |
rs770185155 | snp | G/T | 1.64936e-05 | 0.00287168 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251002 | AATGTCCATCTCCTT[G/T]GGCAGGCCCTGGGCG | 54455 |
rs770188173 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16253231 | CACTGGTATATGAGA[A/C]TAGCCTACCTAGCTC | 54455 |
rs770252743 | in-del | -/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16337344 | ACTAGATGAGAAAAT[-/G]GAATCAACAGGTATT | 54455 |
rs770273430 | snp | A/G | 1.65312e-05 | 0.00287495 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251065 | TCTGGCTCCCAGGAG[A/G]GCCTGGAGAAGACCC | 54455 |
rs770294357 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16264804 | CTAACATTCCCTAAA[A/T]CTGCTAATAGGTTCA | 54455 |
rs770350268 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16278682 | CATTAACGGGACTGA[C/G]AGCCCCATATGTAAC | 54455 |
rs770354625 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16312294 | TTGAGCCCGGGAGAC[A/G]GAGGTTGCAGTGAGC | 54455 |
rs770382628 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16327944 | GACCTCAAGTGATCC[A/G]CCCACCTTGGTCTCC | 54455 |
rs770390622 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16254471 | CATCTCTAACCCTCA[A/C]GGGACCAACATGACG | 54455 |
rs770393748 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16299375 | CTGAGGTCCTTACCA[C/T]ATGTATTTTAATCCC | 54455 |
rs770422021 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16349523 | TCCACATTAACAATC[A/G]TGGGAAGGGCTTTAT | 54455 |
rs770424967 | snp | A/G | 0.000148342 | 0.00861099 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251651 | TCTTACTGGAGACTG[A/G]GAGCGGTACTCTCGG | 54455 |
rs770425025 | snp | A/C | 0.000278024 | 0.0117871 | intron-variant | FBXO42 | GRCh38.p7 | 1:16315142 | AATTTGAAATCAATA[A/C]ATAAACCTTTCTCCT | 54455 |
rs770441496 | snp | C/T | 1.67335e-05 | 0.00289248 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251775 | CTGAAGACCACCACA[C/T]ACTGTCCCACCTGGA | 54455 |
rs770455329 | in-del | -/AAAAAATATAT | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16311499 | TCTCAAAAAAAAAAA[-/AAAAAATATAT]ATATATATATATATA | 54455 |
rs770460393 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16312576 | GAAGCTATTATGATA[C/T]TATAACAGTGGATAT | 54455 |
rs770488444 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16302023 | CTTGCTTCCCACATC[C/T]AAAGGCCTTTCCTTT | 54455 |
rs770535315 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16270690 | AAAAAAAAAAAAAAA[A/G]AAAAAAGAAAAGAAA | 54455 |
rs770559555 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16326702 | AAAAAAAAAAAAAAG[-/A]AAAAAATTATTCTTG | 54455 |
rs770581411 | snp | A/G | 1.75505e-05 | 0.00296225 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250625 | CTTACACACTGGAAA[A/G]TTCCAAATTAAAAGC | 54455 |
rs770596541 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16314239 | ACTGGTGTGAGCCAC[C/T]ACACCCGGCCAAGAA | 54455 |
rs770596908 | in-del | -/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16284654 | GCCAAGATAGTGAAA[-/C]CCCCATCTCTACTAA | 54455 |
rs770652643 | snp | C/T | 1.65718e-05 | 0.00287848 | intron-variant | FBXO42 | GRCh38.p7 | 1:16256581 | CTTTTCTTCCAGATT[C/T]AAAGAGTTTATCTTT | 54455 |
rs770693632 | snp | C/T | 1.7303e-05 | 0.00294129 | intron-variant | FBXO42 | GRCh38.p7 | 1:16255698 | TCATATGGAGCAAAC[C/T]AAATGTACTTACATT | 54455 |
rs770698131 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16325330 | TTTTTAAGTACACAG[C/T]TTAATATTTTAAATT | 54455 |
rs770710454 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16280639 | TTCTAAAATAAAACA[C/G]TATGTTAGCACCTGA | 54455 |
rs770766183 | snp | C/G | | | downstream-variant-500B | FBXO42 | GRCh38.p7 | 1:16246616 | TGGAGCAATTCTCCT[C/G]CCTCAGCCTCCCAAG | 54455 |
rs770783449 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16273620 | GCATGGTGGCTTATG[C/G]CTGTAATCGTAGCAC | 54455 |
rs770814420 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16294663 | ACATGGCACATTAAA[C/T]TTAAGGACCTGAGTC | 54455 |
rs770817622 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16259995 | GACATTTCTATCATT[A/G]CAGAAAGTTCTATTT | 54455 |
rs770882458 | in-del | -/TTTC | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16269836 | GCCTATTCTTTATGT[-/TTTC]TTTCTTTGTTTTTTC | 54455 |
rs770892272 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16339108 | AGCCACCCTGCCCAG[C/T]GGTCATTTATCTTTT | 54455 |
rs770906810 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16279004 | TGGTCTCGAACTCCC[A/G]ACCTCAGGTGATCTG | 54455 |
rs770916100 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16248636 | GTACAGCAATAGCGG[-/T]TAACACCTGAATTGC | 54455 |
rs770926057 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16318632 | AAATGAAGGAAATAG[C/G]GTGTTTTATGTAAGA | 54455 |
rs771031066 | snp | A/G | 1.64999e-05 | 0.00287222 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251398 | AAAGTCCTATTTTCA[A/G]GTCGTATCCTTCAGG | 54455 |
rs771087830 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16285119 | CCCCTGTACTCCAGC[A/C]CCGCGACACTGCAAG | 54455 |
rs771106372 | snp | C/G | 3.29663e-05 | 0.00405981 | missense, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16315389 | CACAGCCATGAAACT[C/G]TCATCTTCACTGTCC | 54455 |
rs771120933 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16252897 | AGAGACAAATATCTA[C/T]GATTAAAAGGATCCC | 54455 |
rs771121806 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16318820 | AACAGAGAGCTCGGG[A/G]GCAAAGACGGCCACT | 54455 |
rs771135172 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16247735 | CAAATTTGTGCTCCC[-/A]AAGTGTAGGGTAGGG | 54455 |
rs771151104 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16344644 | CCCATCCAGTTGTTA[C/T]ATTTTTAAACCTTCT | 54455 |
rs771165851 | snp | A/G | | | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16352497 | GCGCGCATGCGCCGG[A/G]GCGGGCGCGGCGGAC | 54455 |
rs771179059 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16330122 | CTAGACACTAAGCTA[A/G]TTTTACAATGGACAG | 54455 |
rs771188959 | in-del | -/TTCTATGA | 1.72779e-05 | 0.00293916 | intron-variant | FBXO42 | GRCh38.p7 | 1:16251815 | CCAGTGCTCACACTC[-/TTCTATGA]TTCTATGATTCTGAT | 54455 |
rs771190219 | snp | A/G | 1.65638e-05 | 0.00287778 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251448 | GATATGGCCTGTACA[A/G]GACTGTCCAAAGAAG | 54455 |
rs771235040 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16349212 | GACTCTGCAGAATAA[C/T]AGGAAAGGTTGGGGA | 54455 |
rs771305547 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16299159 | TGGGATTACAGGCAT[A/G]TGCCACCATGCCTGG | 54455 |
rs771327863 | snp | C/G | 1.6571e-05 | 0.0028784 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16252404 | AAGCATCCTTGAATA[C/G]CTGTAAGAGAAAAAA | 54455 |
rs771360783 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16312272 | GTGGCTGAGGAGGGA[A/G]GATGACTTGAGCCCG | 54455 |
rs771362471 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16298144 | GGCAGTAGAATCGCT[C/T]GAACCCGGGAGGTGG | 54455 |
rs771407256 | in-del | -/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16307987 | TAGCCAAGAAAACAT[-/G]GAAGGAGGAGAACAA | 54455 |
rs771415030 | snp | C/T | 0.000263674 | 0.011479 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16294805 | CAAAGGTCGGATCCA[C/T]TCTTTGCTGTTTAGG | 54455 |
rs771432391 | snp | A/G | 9.89136e-05 | 0.00703186 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250966 | GGTGGTGGCCCAGGC[A/G]GCGAGCAATGGGAGG | 54455 |
rs771436040 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16303213 | GAAAGGCAGGCAGAA[C/T]GAAAACTCCTACATG | 54455 |
rs771505549 | in-del | -/CTC | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16261937 | CAGGATGGTCTCGAT[-/CTC]CTGACCTTGTGATCC | 54455 |
rs771513406 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16322885 | TCCGTAACCTAGAAA[C/G]AATCAACTCAAAAGA | 54455 |
rs771523348 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16266207 | AAAAATAGAAACATC[G/T]CTTTCATACATATAT | 54455 |
rs771526496 | snp | A/C | 1.65228e-05 | 0.00287422 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251055 | CTGCTCAAACTCTGG[A/C]TCCCAGGAGAGCCTG | 54455 |
rs771555370 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16253296 | CATTCTCCTAAAAAC[A/G]TATCAATTCTGATCC | 54455 |
rs771556899 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16310651 | GTATTTGCAAAAGAC[A/G]TATCTGATAAAAGAC | 54455 |
rs771591957 | snp | C/G | 3.3972e-05 | 0.00412127 | intron-variant | FBXO42 | GRCh38.p7 | 1:16294966 | AATTCTGAGGCCCTT[C/G]CAACATTTTAACCAT | 54455 |
rs771602967 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16338965 | ACAGGTGCACATCAT[C/T]ACCCCCGGCTAATTT | 54455 |
rs771647635 | in-del | -/A | | | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16316731 | CAGAGAAAGACTCTC[-/A]AAAAAAAAAAAAAAA | 54455 |
rs771671619 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16346313 | TAAATAGAAAATATT[C/G]TAAGGGAACATTACC | 54455 |
rs771698666 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16325248 | GTCCCAAAACAACAA[C/T]AACAAAACAGAATTA | 54455 |
rs771703857 | in-del | -/CAAT | | | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16249942 | TGTCAGAAATTTCCA[-/CAAT]CAATCAGACACAAAA | 54455 |
rs771708635 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16312390 | GAAACTTAAATGCAA[A/C]TATTACTAAGTGAAA | 54455 |
rs771724702 | in-del | -/AACAAACA | | | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16317420 | TCGTCTCAACAAACA[-/AACAAACA]AACAAACAAACAAAA | 54455 |
rs771738787 | snp | C/G | | | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16352964 | CACAGAAAACGATCA[C/G]TTATTTGCCCGGAGT | 54455 |
rs771747264 | in-del | -/AACAAACA | | | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16317413 | GAGTGAGATCGTCTC[-/AACAAACA]AACAAACAAACAAAA | 54455 |
rs771751580 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16324291 | AAAAAGAAAAAATAT[A/G]TTATGCTTAGATCCC | 54455 |
rs771763054 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16277883 | CTGTCTCAACAAAAA[A/G]TTTAAAAAATTAGCT | 54455 |
rs771848900 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16337183 | CTTCTCAAATTTTAA[C/T]GTGAATCTAGTTTAT | 54455 |
rs771864379 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16257596 | AATTGCTATTTTTCC[C/T]CATCCCTCACTCTAC | 54455 |
rs771912052 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16256316 | AGCAGCCAAAGCTGA[A/G]GAGCTCGCTGTTCTT | 54455 |
rs771950860 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16258603 | TTCAAGCAATCCTGC[C/T]GCCTTGGCCTTTCGA | 54455 |
rs771957961 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16271822 | CTATACCTGCATACC[A/T]AGCATAGTCATTGGA | 54455 |
rs771964478 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16351656 | CGTTCCCTTTGCACA[C/T]ACAATTCTCGCCAAG | 54455 |
rs771986027 | in-del | -/TAACT | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16330056 | TTTCCCCTACCTTCC[-/TAACT]TGTCTCCACCTAGGT | 54455 |
rs772011414 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16286321 | TTTAATTGACTCACA[A/G]TTCCGCATTGCTGGG | 54455 |
rs772022359 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16342644 | TCCCCTGACCCTTAA[C/T]AGTTTCACCCTACAG | 54455 |
rs772043881 | snp | A/G | 1.84317e-05 | 0.0030357 | intron-variant | FBXO42 | GRCh38.p7 | 1:16255679 | GGAGTATTTACCTTC[A/G]GGCTCATATGGAGCA | 54455 |
rs772053576 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16306105 | TCGGCCACTGCAACC[A/T]CTGCCTCCTGGGTTC | 54455 |
rs772072670 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16348680 | CACTCCAGCCTAGGC[A/G]ATAGAGCAAGACTTG | 54455 |
rs772104705 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16305007 | TTCTTAACAAACTGC[C/G]TACAATATATTTAGG | 54455 |
rs772124571 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | FBXO42 | GRCh38.p7 | 1:16316543 | GAGTTCGAGACCAGC[A/G]TGGGCAACATGGCGA | 54455 |
rs772129973 | snp | A/G | 1.65619e-05 | 0.00287762 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251171 | CAGGGCACCTGGGGA[A/G]ACGGCCCCTGCAAGG | 54455 |
rs772209221 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16284806 | AACCCTGTCTCTACT[A/G]AAAAATACAAAATTA | 54455 |
rs772218277 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16296747 | CATCTAGCATATTTG[C/T]AGGTCTAATTCAGTT | 54455 |
rs772255020 | snp | C/T | 1.65381e-05 | 0.00287555 | intron-variant | FBXO42 | GRCh38.p7 | 1:16252265 | GACCTGTCCTCCTGC[C/T]AGCCTGTCAGCTCCC | 54455 |
rs772269444 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16309419 | TTTCCAAAAATGATG[C/T]TGAAATAAATTAAAA | 54455 |
rs772270574 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16346127 | ACAGAAAGTAGCAAG[A/G]AAACTTATTTGCTAC | 54455 |
rs772273056 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16344034 | CAGAGTTTCACTCAT[A/G]TTGCCAAGGCTGGAG | 54455 |
rs772327584 | snp | A/G | 8.23934e-05 | 0.00641794 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251300 | ATTACTACTGGAAGC[A/G]GGTTTCAGATCCCAA | 54455 |
rs772384260 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16276263 | CATGCACCTGTAGTC[C/G]CAGCTATTCGGGAGG | 54455 |
rs772386093 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16268172 | GGACTTTAAGAAGTG[A/G]AAACAATGTTACCAG | 54455 |
rs772386199 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16249730 | TCTGTAGGCACCTGA[A/G]CTTTGTAAAAGAAAC | 54455 |
rs772477058 | snp | C/G | 3.3264e-05 | 0.0040781 | missense, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16315173 | ATCCACAGTACCTTT[C/G]ATAAGTCGATACCAC | 54455 |
rs772495405 | snp | A/G | 1.64746e-05 | 0.00287002 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16315287 | CTCCGACATGGACCT[A/G]TTATGTCTAGTCTCC | 54455 |
rs772495508 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16322603 | AAATTTTAAAAACTA[A/C]AAAAAAAACTATGCT | 54455 |
rs772504331 | snp | A/T | 1.65184e-05 | 0.00287384 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16252376 | CAAGGACCAGAATGC[A/T]TGTGCAACAACCAAG | 54455 |
rs772524056 | in-del | -/GAG | 3.3077e-05 | 0.00406662 | cds-indel, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251083 | CTGGAGAAGACCCAA[-/GAG]GAGGACTTAGTGCTG | 54455 |
rs772543744 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16290418 | CACAAGAAGCTGGGC[A/T]CAGTGGCTCATGCCT | 54455 |
rs772548437 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16300613 | GTCATGTGTCTCACA[C/G]CTACAAGCCAGAACA | 54455 |
rs772583771 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16275203 | GAGAAGACAAAAAAG[A/G]GACACAACATAAAAG | 54455 |
rs772610418 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16330890 | GAGGTTGCAGTGAGC[C/T]GAGATCCTGCCATTG | 54455 |
rs772613523 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16311177 | GTGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAGG | 54455 |
rs772639202 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16288684 | AAGTCTTGGCCGGGC[A/G]CAGTGGCTCATGCCT | 54455 |
rs772650946 | in-del | -/TT | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16295058 | TCTATTACCAGCCTC[-/TT]GTCTCCAAGTGGATC | 54455 |
rs772674017 | snp | C/T | 0.000131776 | 0.00811608 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250846 | ATACTTTCCATTTGA[C/T]CCGCCCCTTCTCCTT | 54455 |
rs772715779 | snp | A/G | 1.64917e-05 | 0.00287151 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251631 | CAAGGAGCTTCATCC[A/G]TGCTTCTTACTGGAG | 54455 |
rs772737366 | snp | C/T | 1.6549e-05 | 0.0028765 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251551 | GGGAAAGGCTCCCTT[C/T]CCGGGAACCTGAAGG | 54455 |
rs772745108 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16334907 | AGAAGGGTAAACAGT[A/G]ATCCTTAGTATCAGG | 54455 |
rs772787381 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16265123 | TTTGAGACGGAGTTT[C/T]GCTCTTGTTGCCCAG | 54455 |
rs772878861 | in-del | -/TTTTTTTTTTTTTTTTTTTT | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16309058 | GGGAGACCCCATCTC[-/TTTTTTTTTTTTTTTTTTTT]TTTTTTTTGAGACAG | 54455 |
rs772908789 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16312444 | TACTGTATGATTCCA[A/G]CTATATGACCTTCTA | 54455 |
rs772914192 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16266312 | GAATTTGAGGAAAAG[A/G]GCCATGCTAAAATAA | 54455 |
rs772914384 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16325271 | CAGAATTACCTTTAA[C/G]ACAAAACAAAACTAA | 54455 |
rs772917474 | snp | C/G | 1.65886e-05 | 0.00287993 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16253719 | AAGGTCAAGGACCCA[C/G]ACATCATTGCTCCTG | 54455 |
rs772962488 | snp | A/C | | | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16352776 | TTAACTCACTTCTAC[A/C]CCGAGGGCCCGATGA | 54455 |
rs772969602 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16324304 | ATATTATGCTTAGAT[C/T]CCACACAGGGTACAA | 54455 |
rs773128279 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16285641 | CCCCACAAGCTTTCT[A/T]TACTAAATTTAAGGG | 54455 |
rs773131067 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16258616 | GCCGCCTTGGCCTTT[C/T]GAAGTGTTAGGATTA | 54455 |
rs773212745 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16334168 | GCCGGGCCCGGTGGC[A/T]CACGCCTGTAATCCC | 54455 |
rs773227213 | snp | C/T | 1.64841e-05 | 0.00287085 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251272 | CTGTCCTATTGTCCA[C/T]GCCATCCATGGGATT | 54455 |
rs773404153 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16303718 | GATTACAGGTGCCTG[C/T]CACCATACCTGGCTA | 54455 |
rs773411747 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16269254 | TATCATACCCGCCTA[A/C]TTTTCTATATTTTTA | 54455 |
rs773494900 | snp | C/T | 1.65162e-05 | 0.00287365 | intron-variant | FBXO42 | GRCh38.p7 | 1:16252279 | CTAGCCTGTCAGCTC[C/T]CTGCTTACCCGGCAA | 54455 |
rs773550055 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16299961 | CTCAACTATTTTAAG[C/G]ACCCTAGCCTACTGA | 54455 |
rs773551052 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16342854 | GAGTTCTGGCTCTCC[C/G]AAACTAGATTAGTTC | 54455 |
rs773570260 | snp | C/G | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250847 | TACTTTCCATTTGAC[C/G]CGCCCCTTCTCCTTG | 54455 |
rs773572192 | in-del | -/AAT | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16331425 | TCTCAAAAAGAAAAT[-/AAT]AATAATAATAATAAT | 54455 |
rs773578149 | snp | C/T | 1.64773e-05 | 0.00287026 | missense, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16315298 | ACCTATTATGTCTAG[C/T]CTCCTCAGCCTCCAA | 54455 |
rs773580228 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16261856 | CTACAGGCACCCCCC[A/G]CCATGCTCAAGCTAA | 54455 |
rs773584944 | snp | A/G | 1.6534e-05 | 0.00287519 | stop-gained, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250684 | ATTATCTCTTTGCTC[A/G]TACAAAGTACAAGGC | 54455 |
rs773590421 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16249737 | GCACCTGAGCTTTGT[A/C]AAAGAAACAGAAAGT | 54455 |
rs773605769 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16340721 | ACAATGCTTTATACA[A/C]TTTACTGAGCAATAG | 54455 |
rs773606752 | in-del | -/TCTCATACT | 9.89723e-05 | 0.00703394 | cds-indel, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251240 | CTGTTCAGGAGGGTG[-/TCTCATACT]TCCCCCAACTGTCCT | 54455 |
rs773631586 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16275256 | CACAACCCATCATCA[C/T]TTCTAGAGAGAACTA | 54455 |
rs773667927 | snp | C/T | 3.30371e-05 | 0.00406417 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16252377 | AAGGACCAGAATGCA[C/T]GTGCAACAACCAAGC | 54455 |
rs773679686 | in-del | -/ATC | | | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16353516 | TGTCCACAATCCCTT[-/ATC]ATAACCCAGACATTC | 54455 |
rs773718980 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16309523 | AAACATAAAACTCCT[C/T]GAAGATAACAGGAGA | 54455 |
rs773836404 | in-del | -/TT | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16344325 | TGGAATATATATAAT[-/TT]TTTTTTTTTTTTTTG | 54455 |
rs773859172 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16269187 | TCAGCTCCTGGGTTC[-/A]AGCGATTCTCCTGCC | 54455 |
rs773887946 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16271954 | GACCAGCCTAGCCAA[C/T]ATGGTGAAACCCCGT | 54455 |
rs773911706 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16276723 | ATGAAGTACTGTTAG[A/G]AGATTACATGGATAC | 54455 |
rs773915137 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16308155 | ACAGTCCATTCATTT[C/T]TTTTTAATAGAGGTG | 54455 |
rs773921092 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16321558 | ACGTGACTGAATGAA[C/T]GTACTGGAATCTGAA | 54455 |
rs773928900 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16323141 | AAAATGTAATTGGCC[A/G]GGCACAGTGGCTCAC | 54455 |
rs773948768 | snp | C/G | 1.6534e-05 | 0.00287519 | intron-variant | FBXO42 | GRCh38.p7 | 1:16256796 | ATGGTTAGCATTCAG[C/G]ATCTCACAACAATCC | 54455 |
rs773993785 | in-del | -/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16303654 | CTCACTGCAACCTCC[-/G]CCTCCCGGGTTCAAG | 54455 |
rs774036333 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16270708 | AAAAGAAAAGAAAAG[-/A]AAGAAGAAAAGATAA | 54455 |
rs774058677 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16351285 | CATGACAGAAACACA[A/G]TCGAAGTCTCCCAAT | 54455 |
rs774069887 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16349764 | TTACTCAGGAAGCTG[A/G]GGCAGGAGAATCGCC | 54455 |
rs774096837 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16291832 | ACATGCCATCATGCC[C/T]GGCTCATTTTTAATT | 54455 |
rs774121276 | in-del | -/GTGTGT | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16271263 | TGTGTGTGTTGGTGT[-/GTGTGT]GTGTGTGTGTGTGTG | 54455 |
rs774131386 | snp | C/T | 1.6534e-05 | 0.00287519 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251420 | TCCTTCAGGAGCAGA[C/T]GGAGTACTTGGAGAT | 54455 |
rs774147621 | snp | C/T | 1.65548e-05 | 0.002877 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251530 | GAGAGCCGTCTCCTC[C/T]GGCTGGGGAAAGGCT | 54455 |
rs774219130 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16261826 | CTCCTGCCTCAACCT[C/T]CTGAGTAGCTGGGAC | 54455 |
rs774225818 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16248424 | TCTAAGACAATCAAC[A/G]TATCTGTTGCCTGCC | 54455 |
rs774248796 | snp | C/T | 1.65537e-05 | 0.0028769 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251098 | GAGGAGGACTTAGTG[C/T]TGCAGAGGCCGAGGG | 54455 |
rs774252708 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16313700 | CTTGATGCAAGGAAA[A/T]CATTTTAAAACTGAT | 54455 |
rs774263525 | snp | A/G/T | 8.45638e-05 | 0.006502 | intron-variant | FBXO42 | GRCh38.p7 | 1:16253210 | GGTTTCTGACTTTCT[A/G/T]TGCTTCACTGGTATA | 54455 |
rs774291316 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16303449 | AGCAATGACTTTACA[C/G]ATTTCTTACAGATTT | 54455 |
rs774296906 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16349806 | GGTGGAGGTTGCAGT[A/G]AGCCGAGATCATTGC | 54455 |
rs774332311 | snp | C/T | 3.29669e-05 | 0.00405984 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251664 | TGAGAGCGGTACTCT[C/T]GGGTTTCAGGAACGA | 54455 |
rs774340876 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16282705 | ATGCTGATCGGCTGA[C/G]TGCAGTGGCTCATGC | 54455 |
rs774378236 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16282902 | AGGAGAACTGCTTGA[A/T]CCCAGGAGGCAGAGG | 54455 |
rs774379649 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16340615 | TGAGCCACTGCGCCC[A/G]GCCAACCCTCTACTG | 54455 |
rs774399103 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16269055 | ACCTCGTGATCCACC[C/T]ACCTCGGCCTTCCAA | 54455 |
rs774429075 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16296380 | ATTCAGGCCAGGTGC[A/G]GTGGCTCATGCCTGT | 54455 |
rs774431151 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16281308 | TATAGTATCATCCTA[C/T]TGAGTTGATATGAAG | 54455 |
rs774468484 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16328653 | CATGTGTTAGTATAC[A/G]CTCATCTACCACCTT | 54455 |
rs774487605 | snp | A/G | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16316445 | CACTTACAAAATATA[A/G]TAGTTCTTGGTTGGG | 54455 |
rs774505454 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16309298 | TGGCCAGGATGGTCT[C/G]AATCTCTTGACCTCA | 54455 |
rs774523083 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16342707 | TTAGATAAGGTTTGT[C/T]GCCACCAAAACTCAT | 54455 |
rs774544026 | snp | A/G | 3.35115e-05 | 0.00409324 | intron-variant | FBXO42 | GRCh38.p7 | 1:16315165 | TTTCTCCTATCCACA[A/G]TACCTTTGATAAGTC | 54455 |
rs774607164 | snp | A/G | 1.65677e-05 | 0.00287812 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251157 | TCCAGACTCCGACGC[A/G]GGGCACCTGGGGAGA | 54455 |
rs774630314 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16249563 | GTGCTCAATGTGCTT[C/T]GGAAGTAAAAAGAAG | 54455 |
rs774654712 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16319087 | AAATTTCCAGCATTC[C/T]CTCTAGCACTGATGA | 54455 |
rs774701441 | snp | C/T | 1.743e-05 | 0.00295206 | intron-variant | FBXO42 | GRCh38.p7 | 1:16251821 | GCTCACACTCTTCTA[C/T]GATTCTGATTGTTCA | 54455 |
rs774764935 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16287773 | CATTTAAGGGAAGTC[A/G]GGCCCTTTGTTTTCA | 54455 |
rs774787805 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16260694 | TTATTCTGGATTTTA[A/G]TTTTTAATTTTATTT | 54455 |
rs774791997 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16275142 | CAATAGCAAGAAACA[C/T]TCTGAGATTCAGCAG | 54455 |
rs774906930 | snp | A/C/T | 5.03135e-05 | 0.00501544 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250668 | AAGGGGTTTAGAACA[A/C/T]ATTATCTCTTTGCTC | 54455 |
rs774909364 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16288576 | TTATTTTCCACTTCA[C/G]CAAATGGCCCCACCA | 54455 |
rs774931296 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250831 | CAGAACTGCTATTAA[A/G]TACTTTCCATTTGAC | 54455 |
rs774937777 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16333116 | CTCTTCTTGAGGTTC[C/T]ATCCCCTCCAGCCAA | 54455 |
rs775075185 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16290841 | TCCAGCCTCTAGAAC[C/T]GTGAGAAATACATTT | 54455 |
rs775075805 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16268815 | CTAAAAACGAACAAA[C/T]AAACGAACAAAAAAA | 54455 |
rs775104969 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16309654 | TAATCCCAACACTTT[C/G]GGAGGCCAAGGTGGG | 54455 |
rs775120872 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16302231 | ATGACTTTTAGAGAA[A/C]AGGACACTTTCAGTC | 54455 |
rs775138521 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16335270 | TCAACTTCCCAAGAA[G/T]CTGGGACTCCAGGTG | 54455 |
rs775176008 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16315424 | AGCTGGCCATGACAT[C/T]CCACTCAACAGCTGT | 54455 |
rs775190912 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16289163 | ACTTTGGGAGGCCAA[C/G]GCAGGAGGATCATTT | 54455 |
rs775250433 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16349723 | AAAAATTAGCTGGGC[A/C]TGATGGCAGGCACCT | 54455 |
rs775253468 | in-del | -/AC | 0.0123615 | 0.0776397 | intron-variant | FBXO42 | GRCh38.p7 | 1:16252455 | GATATGCGTTCCAAA[-/AC]ACACACACACACAGA | 54455 |
rs775269054 | snp | A/G | 1.64808e-05 | 0.00287057 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16256623 | ATTTTTAGAGGGTGA[A/G]TAAGTGTGTATTTCA | 54455 |
rs775274176 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16282699 | TTAAAAATGCTGATC[A/G]GCTGAGTGCAGTGGC | 54455 |
rs775278172 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16303280 | GCAAGGCTAGTTGCA[C/T]GTTTCAGACTTGCAG | 54455 |
rs775289100 | snp | C/G | 3.30278e-05 | 0.0040636 | intron-variant | FBXO42 | GRCh38.p7 | 1:16256779 | GGAAAGTCAGTAACA[C/G]CATGGTTAGCATTCA | 54455 |
rs775291125 | snp | C/G | 4.94368e-05 | 0.00497152 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251302 | TACTACTGGAAGCGG[C/G]TTTCAGATCCCAATT | 54455 |
rs775302171 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16348682 | CTCCAGCCTAGGCGA[C/T]AGAGCAAGACTTGGT | 54455 |
rs775374928 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16282537 | GGCCATTTTCTCTTT[A/T]AAAAAAAAAAAAAAT | 54455 |
rs775392941 | snp | A/T | 1.80078e-05 | 0.0030006 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16253152 | CATCATCTATGACAA[A/T]CTGAGGAGGGGAAGA | 54455 |
rs775420738 | snp | A/G | 1.65247e-05 | 0.00287438 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16315407 | ATCTTCACTGTCCGA[A/G]GAGCTGGCCATGACA | 54455 |
rs775437238 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16314571 | ATAAAAGCTATGTTC[A/C]CATTGGCTATTACTA | 54455 |
rs775479577 | in-del | -/TA | | | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16247888 | ACTAAAATTCTTAAG[-/TA]TAAGATGGACAAGGT | 54455 |
rs775484079 | snp | G/T | | | intron-variant, utr-variant-5-prime | FBXO42 | GRCh38.p7 | 1:16261073 | TACATTCCTTCTGAA[G/T]AGTTGCCACAAACAA | 54455 |
rs775494552 | snp | A/G | 1.64806e-05 | 0.00287054 | missense, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16315322 | CCTCCAATACTGGGT[A/G]GGGCTCCTCATCTTG | 54455 |
rs775504044 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16326953 | CCTAATCCCAAAAGG[G/T]GTCAACCAGGAAGCC | 54455 |
rs775549577 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16307363 | AAAATTAGCCAGGCA[C/T]GGTGGTCTGCACTTG | 54455 |
rs775551520 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16293546 | CATCTGCAGACTGGA[A/C]CACCACCCTCCTACC | 54455 |
rs775566661 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16260477 | GCCTCCCAAAGTGCT[A/G]GGATTACAGGTGTGA | 54455 |
rs775642496 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16320081 | AAAACGTACAGTCGC[C/T]GAGCATGGTGGCTCA | 54455 |
rs775657334 | in-del | -/AGAG | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16335471 | TAATCTGCCACAATT[-/AGAG]AGAATTAGCTGGTTT | 54455 |
rs775692987 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16342774 | GTGGGGCCTACTGGG[C/T]GGTGTTTAGGTAATG | 54455 |
rs775702326 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16325695 | AGAGTCTGGCTTTGT[C/G]ACCTAGGCTGGAGTG | 54455 |
rs775743618 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16306536 | ATATTATTTACTCCA[A/G]AGCAAAGGTGTTGGG | 54455 |
rs775755161 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16339626 | ATAGTTATGTTCTTA[A/T]GTAAATTTTCTCAAT | 54455 |
rs775762526 | snp | C/T | 3.30311e-05 | 0.0040638 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16253680 | GGGGCCAGAGATGTT[C/T]GGCTTGGACCACGCC | 54455 |
rs775769573 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16310699 | AAAGAACTCTTAAAA[C/G]TCAACAATATTAGGG | 54455 |
rs775873339 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16319306 | ATTCATGCACTAATT[A/G]TGTGTAACATCTTTT | 54455 |
rs775874122 | snp | C/T | 9.88484e-05 | 0.00702954 | missense, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16294851 | TCATTGAAAGCAGCA[C/T]TGCAGCTGCTCTGGG | 54455 |
rs775903563 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16318969 | CTCCTTACAGATGGA[C/T]AGTAAGTCCTTTTGA | 54455 |
rs775917731 | snp | G/T | | | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16353673 | ACCTTAGCCTCCTGA[G/T]TAACTGGGACTACAG | 54455 |
rs775941658 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16253244 | GAATAGCCTACCTAG[C/T]TCCCAAATGGGAATA | 54455 |
rs775953606 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16272443 | TTTGTATTTTAAGTA[A/G]AGACCGGGTTTCACC | 54455 |
rs775958504 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16331777 | TAAATGCAGCCAGGC[A/G]CGGTGGCTCATGCCT | 54455 |
rs775959672 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16287633 | GCTCTTGCTATGTTG[C/T]TCAGGCTGGTCTTGA | 54455 |
rs775964146 | snp | A/G | 1.64735e-05 | 0.00286993 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16305804 | CAGTAAATACTTACT[A/G]TGCGAGAAGCGCTGA | 54455 |
rs775964452 | snp | A/G/T | 6.61949e-05 | 0.00575271 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251561 | CCCTTCCCGGGAACC[A/G/T]GAAGGAGTCTGCCTT | 54455 |
rs775982723 | snp | C/G | 3.29669e-05 | 0.00405984 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251652 | CTTACTGGAGACTGA[C/G]AGCGGTACTCTCGGG | 54455 |
rs775996991 | snp | C/T | 0.000131952 | 0.0081215 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251735 | CAAACTGGGGCTGAG[C/T]GGGGCTCTCCCACTA | 54455 |
rs776006894 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16286835 | AGGATAAAAACCTGA[A/G]GAGTCATCTTGATTG | 54455 |
rs776082478 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16346173 | TTCACCAATTCTTTA[C/T]GAAGAAATTTATAAT | 54455 |
rs776083619 | snp | C/T | | | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16353773 | CTCTCATCTCAAACT[C/T]CTGAGCTCAAGTAAT | 54455 |
rs776149939 | snp | C/T | | | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16352653 | CCTCCGCACCCGCCT[C/T]CGCCGCGTCTCTAGC | 54455 |
rs776161397 | snp | A/G | 1.71552e-05 | 0.0029287 | intron-variant | FBXO42 | GRCh38.p7 | 1:16255701 | TATGGAGCAAACCAA[A/G]TGTACTTACATTTGC | 54455 |
rs776172681 | in-del | -/CAGA | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16254761 | CTGCTACCGCTGAAT[-/CAGA]CAGTGATACAGATGG | 54455 |
rs776196585 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16253420 | TCTTGAGAAATGACA[C/T]AGCAAAGTAAATGCT | 54455 |
rs776234764 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16333196 | CTCAAAGTTATATAA[A/G]TATTTGTTGAGAGAG | 54455 |
rs776239192 | snp | C/G | 1.75582e-05 | 0.0029629 | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250628 | ACACACTGGAAAATT[C/G]CAAATTAAAAGCCAC | 54455 |
rs776256773 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16320752 | TTTTTGGTAGAAACA[A/G]GGTTTCACCATGTTA | 54455 |
rs776272241 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16314338 | GTTTTCAAGAAAGCA[A/G]TTGCTAAAAGTAGCT | 54455 |
rs776282635 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16346515 | AACACAGTGAAACCC[C/T]GTCTCCACCAAAAAT | 54455 |
rs776285556 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16348493 | CACATGGTCAGGAGT[G/T]CGAGACCAGCCTGGC | 54455 |
rs776307511 | in-del | -/TC | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16326989 | ACTTACACAGCACCA[-/TC]TCTCTCTCACCATCT | 54455 |
rs776335270 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16300724 | GCATGATGAGCATTG[G/T]GTATGAAACTACCTG | 54455 |
rs776342907 | in-del | -/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16282289 | GGAGTGCAGTGGCGC[-/G]ATCTCGGCTCACTGC | 54455 |
rs776344257 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16254598 | TCCTAAACTCTCTCA[C/T]TGGGAGAGTAGCTCC | 54455 |
rs776446272 | in-del | -/CCTC | | | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16247546 | GTTTTCTTTCTTCCT[-/CCTC]CTCCTCCTCTTTTCT | 54455 |
rs776522030 | snp | C/T | | | downstream-variant-500B | FBXO42 | GRCh38.p7 | 1:16246654 | GATTACAGGTGCCTG[C/T]CACCATGCCCGGCTA | 54455 |
rs776526378 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16292214 | AAATGATTGAAGCAG[C/T]TATTTCTCCAATATT | 54455 |
rs776575033 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16260369 | GTATACTGCCACGCC[C/T]GGCTAATTTTTTGTA | 54455 |
rs776578650 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16279065 | ACAGGCATGAGCCAC[C/T]GCGCCCAGCCTAGAC | 54455 |
rs776581476 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16305377 | TGGGTGACAGAGTGA[C/G]ACTCCATTTCAAAAT | 54455 |
rs776610773 | snp | A/G | 1.64811e-05 | 0.00287059 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251291 | ATCCATGGGATTACT[A/G]CTGGAAGCGGGTTTC | 54455 |
rs776614094 | snp | C/T | 3.29538e-05 | 0.00405904 | missense, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16315304 | TATGTCTAGTCTCCT[C/T]AGCCTCCAATACTGG | 54455 |
rs776626700 | in-del | -/ACTGA | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16299972 | TAAGCACCCTAGCCT[-/ACTGA]ACTTTACTTATTGCC | 54455 |
rs776642368 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16292439 | GGGACTATGGAGGCA[C/T]GCCACCATGCCTGGC | 54455 |
rs776645321 | in-del | -/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16306905 | GGAAAGTTTGTTTTC[-/T]TTTTTTTTTCTTTTT | 54455 |
rs776651386 | snp | C/T | 3.30175e-05 | 0.00406296 | missense, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16315189 | ATAAGTCGATACCAC[C/T]GTTTGCAGACAAGGG | 54455 |
rs776652420 | in-del | -/GGT | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16253920 | TCTGAACCAGAAAGA[-/GGT]GACCATGTTGCTGAA | 54455 |
rs776695030 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16293292 | TGCCCAGCTAATTTT[C/T]GTATTTTTAGGAGAG | 54455 |
rs776700851 | in-del | -/AAAGAAAGAAA | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16313361 | AAGAAAGAAAGAAAG[-/AAAGAAAGAAA]GAGAAAAGAAAGAAA | 54455 |
rs776764421 | in-del | -/A | 3.31851e-05 | 0.00407326 | intron-variant | FBXO42 | GRCh38.p7 | 1:16252413 | GAATAGCTGTAAGAG[-/A]AAAAAACCAATAACA | 54455 |
rs776834923 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16337528 | TCATAGGACTCCATT[C/T]ATTCTTTTTAAGAGA | 54455 |
rs776836779 | snp | C/T | | | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16354343 | CAGGGTCTCACTCTT[C/T]GCCCAGGCTGGAGTG | 54455 |
rs776843216 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16289523 | GTCTTTATCTCAACT[C/T]CCCCTGTGCCACTCT | 54455 |
rs776862300 | in-del | -/AC | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16301685 | AAAAAAAAAAAAACA[-/AC]ACAAAAAAAAAAGAA | 54455 |
rs776880087 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16346691 | GACTCCGTCTCGGGG[-/A]AAAAAAAAAAAAAAA | 54455 |
rs777026418 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16349365 | TTCAGACCAAAAGCT[G/T]TCTTAAATTAGTACC | 54455 |
rs777083858 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16344673 | CTTATACATACATAG[A/G]ATAAAGCAAATAAAT | 54455 |
rs777115195 | snp | C/T | 3.32353e-05 | 0.00407634 | intron-variant | FBXO42 | GRCh38.p7 | 1:16256811 | GATCTCACAACAATC[C/T]GTAGTTAGGCTATCC | 54455 |
rs777136685 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16298153 | ATCGCTCGAACCCGG[G/T]AGGTGGAGGTTGCAG | 54455 |
rs777272949 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16247840 | ACCTGTGAAATAAGA[A/G]AACAGGAAGCTCTGT | 54455 |
rs777294565 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16328027 | AAACAATCAAAATGA[C/T]AGACATATCCAAGTC | 54455 |
rs777307073 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16281872 | ATGCTGGCCAGGCTG[C/T]TCTCAAACTCTTGAC | 54455 |
rs777330939 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16310674 | TAAAAGACAGTTATA[C/T]AGAATATCCAAAGAA | 54455 |
rs777350734 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16282299 | GGCGCGATCTCGGCT[C/G]ACTGCAACTTCTGCC | 54455 |
rs777363085 | in-del | -/TT | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16256529 | TTCTCAAAGGGACTC[-/TT]GACACAAAAAAACAA | 54455 |
rs777380141 | in-del | -/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16315996 | ACAAACATGGAGAAA[-/C]CCCGTCTCTACTAAA | 54455 |
rs777383786 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16314928 | TTAACCAGATCAACT[C/T]TAAGAATATGAAGCT | 54455 |
rs777385776 | in-del | -/AAAAAAAAAAAA | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16341610 | GAGACTGCGTCTTTT[-/AAAAAAAAAAAA]AAAAAAAAAAAAAGT | 54455 |
rs777414054 | in-del | -/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16329451 | AGCCAGGCGTGGCGG[-/T]TGTGCGCCTGTAGTC | 54455 |
rs777436178 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16261376 | CTTTCCAAAACGACG[A/T]CTCAGATATCTTGAC | 54455 |
rs777445926 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16306170 | GGGATTACAGGTACC[C/T]GCCACCATGCCCAGC | 54455 |
rs777464488 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250759 | GTCCTCCAAATATGA[C/T]GAGTTCACCCCTGCC | 54455 |
rs777484644 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16274834 | TGATCTCGTAATCTG[C/T]CCGCCTCAGCCTCCC | 54455 |
rs777488439 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16259708 | GAGGTGGAGGTTGCA[A/G]TGAGCCGAGATTGAG | 54455 |
rs777512303 | snp | G/T | | | downstream-variant-500B | FBXO42 | GRCh38.p7 | 1:16246401 | TTTTTTAGAGATGGG[G/T]TCTCACTATATTGCC | 54455 |
rs777563963 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16280514 | TTCAATGGCAAAAAC[C/T]GCAATTACTTTTGCA | 54455 |
rs777568896 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16292210 | ATGTAAATGATTGAA[A/G]CAGTTATTTCTCCAA | 54455 |
rs777587846 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16307134 | CCACCTCAGGCGATC[C/T]ACCCGCCTAAGCCTC | 54455 |
rs777601779 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16338974 | CATCATCACCCCCGG[C/T]TAATTTCTGTATTTT | 54455 |
rs777620780 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16294439 | CAATAGCTTCTGTCA[A/G]TCAACTACAGTTCTC | 54455 |
rs777624579 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16319378 | TCATAAAATTGCTTC[C/T]CAGATAATTTATCTA | 54455 |
rs777626136 | snp | C/T | | | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16318504 | TTTAAAAATGTCTTG[C/T]TTCTGCTTATCTGTA | 54455 |
rs777645121 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16260073 | TATGCTTGGGGATTA[C/T]GGGAAAGTAGCAGGG | 54455 |
rs777679382 | in-del | -/TGTG | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16280948 | GGTTTCCTCACTTGT[-/TGTG]TGTGTGTTTGTTTTT | 54455 |
rs777680885 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16273490 | AAGTAGGAAATGAGT[G/T]CATATATCCACTGAA | 54455 |
rs777737641 | snp | C/G | | | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16354271 | CCTCGGCCTTCCAAA[C/G]TTCTGGGATTACAGG | 54455 |
rs777867880 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16286409 | CCCAGGGCAGCAGGA[C/T]GGAATGAGTGCAAGC | 54455 |
rs777881772 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16264570 | ACCAAATGTGCCCAC[A/G]TCAAGCGTAGATGAA | 54455 |
rs777919829 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16298889 | CATGATTTCATAACT[A/G]AAAGAGTCAAGGGTT | 54455 |
rs777931288 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16277236 | GTTAATCATCATCCA[C/T]TTCTTCCCCATTGCC | 54455 |
rs777933449 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16274797 | GGGTTTCATCACGTT[A/G]GCCAGGATTCTCTCG | 54455 |
rs777938725 | snp | A/G | 1.64969e-05 | 0.00287196 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251391 | GCCAAAGAAAGTCCT[A/G]TTTTCAGGTCGTATC | 54455 |
rs777953633 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16335344 | GATTTCGCCACATCG[C/T]CCAGGCTGGTCTCAA | 54455 |
rs777985659 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16348816 | GGAAAAAGGAGACAG[C/T]ACTAATAACCACCTA | 54455 |
rs778009520 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16313061 | TGGCCTCCCAAAGTG[C/T]TGGGATTACAGGCGT | 54455 |
rs778028163 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16265735 | TTTAATGAAAGAAGA[C/G]TTAATCCCTTGTCCT | 54455 |
rs778061329 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16252674 | CTTGCCCATAATTTT[A/G]TGTGTATGTATTGGG | 54455 |
rs778075400 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16278402 | AAACCACATCCAGCT[A/G]TTTCAATGTTAGCAC | 54455 |
rs778152868 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16302898 | GCCCCCATGATCCAG[C/T]CTCCTCCCACCAGGT | 54455 |
rs778209479 | snp | A/G | | | utr-variant-5-prime | FBXO42 | GRCh38.p7 | 1:16352446 | GCCGCCGCCGCCGCA[A/G]CTGCTGCTGCTCAGG | 54455 |
rs778223820 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16278718 | TAAGGTATCATTTAC[A/C]CTGTAAAAGAAACAG | 54455 |
rs778225817 | snp | C/G | 1.65124e-05 | 0.00287331 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251042 | CACTGTTTCTCCACT[C/G]CTCAAACTCTGGCTC | 54455 |
rs778235987 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16338570 | TGCCTCATCAATCTA[A/G]AGATTATTCTGCAGT | 54455 |
rs778239679 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16291442 | CTGGGGTGCTGTGGC[A/G]CAATCTTGGCTCACT | 54455 |
rs778241299 | snp | C/T | 1.64817e-05 | 0.00287064 | missense, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16315379 | CTTCCTGGTCCACAG[C/T]CATGAAACTGTCATC | 54455 |
rs778255647 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16323487 | AATAAAATAAAGGAC[G/T]GAGACCTAACTAAAG | 54455 |
rs778288761 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16304615 | CCTCTTAGATAATGT[C/G]AGATGTTTAAAACGC | 54455 |
rs778364339 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16325189 | GCTGCAGTGAGCCAA[C/T]ATCATGCCACTGCAC | 54455 |
rs778366858 | snp | A/G | | | upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16354199 | TTCAGTAGAAAATAC[A/G]GGGTTTCACCATCTT | 54455 |
rs778402545 | snp | C/T | 1.69896e-05 | 0.00291454 | intron-variant | FBXO42 | GRCh38.p7 | 1:16253077 | ATGCACATGGGAATG[C/T]CACAGAAGCAATACT | 54455 |
rs778406535 | snp | G/T | 1.64852e-05 | 0.00287094 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250964 | AGGGTGGTGGCCCAG[G/T]CGGCGAGCAATGGGA | 54455 |
rs778407824 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16259513 | TCACACCTGTAATCC[C/T]AGCACTTTGGGAAGC | 54455 |
rs778408427 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16336242 | CGCGTCTGGCCTAAT[A/C]TTACTTTTTGTGTGC | 54455 |
rs778417932 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16292965 | GCCTGGGTGACAAAG[C/T]AAGATCTTGTCTCAA | 54455 |
rs778419403 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16338887 | ACAATCGCGGCTCAC[C/T]GCAACCTCCGCCTCC | 54455 |
rs778424662 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16294209 | CCATTGTTTTTATTT[C/T]TTCCCCCAGGAGAGG | 54455 |
rs778472666 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16337091 | CACAGCAAAAACAAC[C/T]GTCCAAAGATAAAAG | 54455 |
rs778488633 | snp | A/G | 8.48932e-05 | 0.00651455 | intron-variant | FBXO42 | GRCh38.p7 | 1:16253600 | CTGAAAGACGCTACA[A/G]TGTTTGCTGAATAGT | 54455 |
rs778522371 | snp | C/T | 1.64914e-05 | 0.00287149 | missense, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16305919 | CACTGATGGGCTACA[C/T]CTAAGACAGAAAGAG | 54455 |
rs778526594 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16288031 | GGCGCCTGTAATCTC[A/T]GCTACTTGGGAGGCT | 54455 |
rs778629301 | snp | A/G/T | 3.37201e-05 | 0.00410599 | intron-variant | FBXO42 | GRCh38.p7 | 1:16294960 | TGTGAAAATTCTGAG[A/G/T]CCCTTCCAACATTTT | 54455 |
rs778701045 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16256160 | TAACAGCTAACAAGC[A/G]CCACGTACTAAGTCT | 54455 |
rs778716983 | snp | C/T | 1.65217e-05 | 0.00287412 | | | GRCh38.p7 | 1:16251604 | CTCAGTGTTCCCCAG[C/T]GGCCGTTAACACAAG | 54455 |
rs778722720 | snp | A/G | | | | | GRCh38.p7 | 1:16318413 | ACAGAGCAAGACTCC[A/G]TCTTAAATAAATAAA | 54455 |
rs778726794 | in-del | -/A | | | | | GRCh38.p7 | 1:16350573 | CTCTACTAAAATTAC[-/A]AAAAAAAAAAAAAAA | 54455 |
rs778759920 | snp | C/T | | | | | GRCh38.p7 | 1:16352590 | GAGAAAGGCCGTGGT[C/T]ACAGGCCGAGGTTCT | 54455 |
rs778767862 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16298762 | TGATCCGCTCGCCTC[A/G]GCCTCCCAAAGTGCT | 54455 |
rs778770801 | in-del | -/AA | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16316170 | CAAACCTCCATCTCA[-/AA]AAAAAAAAAAAAAAA | 54455 |
rs778782012 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16329853 | ACTCGGGAGGCTGAG[C/G]CAGGAGAATTACTTG | 54455 |
rs778797259 | in-del | -/AAAAAAAAAA | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16341612 | GACTGCGTCTTTTAA[-/AAAAAAAAAA]AAAAAAAAAAAAAGT | 54455 |
rs778818139 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16286134 | TCAGCCTCCCAAAGT[A/G]CTGATTTTACAGGCG | 54455 |
rs778820811 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16311991 | CAGTAAGTGAATGGG[G/T]AAACAAACTGTGGTG | 54455 |
rs778833276 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16343811 | CTGGGTGACAGAGAC[C/T]ACGTCTCAAAAAAAA | 54455 |
rs778856459 | snp | A/G | | | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16317171 | ACCCGTAATCCCAGC[A/G]CTTTGGGAGGCTAAG | 54455 |
rs778875251 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16284758 | GGATCATCTGAGGTC[A/G]GGAGTTTGAGACCAG | 54455 |
rs778920381 | snp | C/T | 1.86586e-05 | 0.00305434 | intron-variant | FBXO42 | GRCh38.p7 | 1:16255671 | TATTCCCAGGAGTAT[C/T]TACCTTCAGGCTCAT | 54455 |
rs778924551 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16297657 | ATGAAGTCAGCAGAT[A/C]GAGACCATCCTGGCT | 54455 |
rs778972553 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16345543 | TCCTGGTTTCTACTG[C/G]CATTCCCTGTAAAAG | 54455 |
rs779026318 | snp | C/T | | | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251230 | CACCATTTGTCTGTT[C/T]AGGAGGGTGTCTCAT | 54455 |
rs779064635 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16310303 | GAGGTGGAGGTTGCA[A/G]TGAGCTGAGACTGCG | 54455 |
rs779067946 | snp | A/G | 6.60044e-05 | 0.00574438 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251233 | CATTTGTCTGTTCAG[A/G]AGGGTGTCTCATACT | 54455 |
rs779077497 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16264509 | TGCACAAAAGTGAAG[A/T]AAGGAAGGGTGTCAT | 54455 |
rs779190604 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16247233 | AGAGGCTACATGGGA[C/T]GCAGGCCTGGAAATT | 54455 |
rs779190739 | snp | C/G | 1.64947e-05 | 0.00287177 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251371 | GTAGTGATCCTCGTC[C/G]GGGGGCCAAAGAAAG | 54455 |
rs779205389 | snp | A/C/T | 8.30467e-05 | 0.00644339 | intron-variant | FBXO42 | GRCh38.p7 | 1:16256573 | TTTAAGGCCTTTTCT[A/C/T]CCAGATTTAAAGAGT | 54455 |
rs779232064 | in-del | -/ACA | 1.7436e-05 | 0.00295258 | cds-indel, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250642 | TCCAAATTAAAAGCC[-/ACA]GAAAAGGAAAGGGGT | 54455 |
rs779251452 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16322334 | TGTAATCCCAGCACT[C/T]TGGGAGGCTGAGGTG | 54455 |
rs779374372 | in-del | -/TTT | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16344324 | ATGGAATATATATAA[-/TTT]TTTTTTTTTTTTTTG | 54455 |
rs779377143 | snp | A/C/T | 1.64822e-05 | 0.00287068 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251285 | CATGCCATCCATGGG[A/C/T]TTACTACTGGAAGCG | 54455 |
rs779379541 | snp | A/G | 1.70035e-05 | 0.00291572 | intron-variant | FBXO42 | GRCh38.p7 | 1:16253071 | AGTAGCATGCACATG[A/G]GAATGCCACAGAAGC | 54455 |
rs779381034 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16302858 | AAAATTCTTTCACTA[A/T]AACAAGAACAGCATG | 54455 |
rs779381956 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16330508 | TGAGATCCTGTCCCC[C/T]ACAAAAATTAATTTA | 54455 |
rs779388189 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16336099 | CCTGCCACCATGCCC[A/G]GCTAATTTTTCTGTT | 54455 |
rs779439711 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16316009 | AACCCCGTCTCTACT[A/G]AAAATTGAAAATTAG | 54455 |
rs779475583 | snp | C/T | 1.65086e-05 | 0.00287298 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16252367 | TGCCAGGCCCAAGGA[C/T]CAGAATGCATGTGCA | 54455 |
rs779503936 | in-del | -/CAC | 1.654e-05 | 0.00287571 | intron-variant | FBXO42 | GRCh38.p7 | 1:16256801 | TAGCATTCAGGATCT[-/CAC]AACAATCCGTAGTTA | 54455 |
rs779545276 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16271266 | GTGTGTTGGTGTGTG[G/T]GTGTGTGTGTGTGTG | 54455 |
rs779575590 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16305696 | TCCAGCTTGGGTGAT[A/G]GAGTGAGACCTTGTC | 54455 |
rs779598079 | in-del | -/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16265858 | TTGGTCCCTGATCTG[-/C]CATACTACACAGTTG | 54455 |
rs779600357 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16286037 | GACTATAGGTTCACA[C/T]CACGCCCAGCTAATT | 54455 |
rs779648564 | snp | G/T | 1.64781e-05 | 0.00287033 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250919 | GTTCATACTCTGGTA[G/T]AGGGGTTTGCCAACA | 54455 |
rs779738744 | snp | A/T | 1.65031e-05 | 0.00287251 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251033 | AGGGATGGGCACTGT[A/T]TCTCCACTGCTCAAA | 54455 |
rs779765793 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16258263 | TTGTGATCTCACTTA[C/G]GGGAACAATACGATT | 54455 |
rs779771406 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16297706 | CTCTACTAAACATAC[-/A]AAAAAAAAAAATTAG | 54455 |
rs779815336 | in-del | -/AAA/AG | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16350748 | GAGAAACTGCAAAAA[-/AAA/AG]AAAAAAAAAAAAGAA | 54455 |
rs779818506 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16257231 | CTGGATGTCTGGATG[A/C]AACTTAAAAATAACT | 54455 |
rs779830037 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16249415 | TCAAGTACATGATTC[C/T]CAACTCCATCACCTG | 54455 |
rs779835455 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16284549 | TCATCTTAAAAAAAC[A/G]AGCTGGGCGTGGCAG | 54455 |
rs779837072 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16287505 | ATATAGAACAATACC[-/A]GGGGGGCAATCCATG | 54455 |
rs779918768 | snp | G/T | | | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16317003 | AGAAGATAGAAGGCC[G/T]GATGCAGTGGCTCAC | 54455 |
rs779956908 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16322169 | TGGTCAGAATTAATA[C/T]AAATCTCTGGTTTAT | 54455 |
rs779965935 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16283182 | AGGCCCAGAGAATGC[-/A]AAAAAATGATTAAAT | 54455 |
rs779970236 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16316330 | CTTTGCCACAAAATA[A/T]CTCTTTTGTTACTGT | 54455 |
rs780004430 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16296109 | TCTAGAAAAGATGCA[C/T]GAGTGCTAAGTTCTG | 54455 |
rs780018955 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16328481 | CAAATTTTCTTATTG[A/G]AGTGGGAATTTACAA | 54455 |
rs780059439 | in-del | -/TGT | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16330012 | AATTCGTGTATGTAC[-/TGT]GTTTTCCTCTCACAG | 54455 |
rs780059473 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16308853 | GGTTCAAATGATTTC[C/T]CTGCCTCAGGTTCCC | 54455 |
rs780120799 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16261630 | CATACAAGAACAAAT[G/T]AGGTGGCAGAGATCA | 54455 |
rs780140736 | in-del | -/CTT | | | cds-indel, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16247558 | CCTCCTCCTCCTCCT[-/CTT]TTCTTTATTTTAAAG | 54455 |
rs780196518 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16321322 | TTGCATAGCCCTTCT[C/T]TTTCACTTCCATGAT | 54455 |
rs780205016 | snp | A/G | 1.65436e-05 | 0.00287602 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251585 | CTGCCTTTGAGCCCT[A/G]GGTCTCAGTGTTCCC | 54455 |
rs780210121 | snp | A/G | 3.54478e-05 | 0.00420983 | intron-variant | FBXO42 | GRCh38.p7 | 1:16253775 | TAGTTAGGAGCTCCC[A/G]GGGACCATAATGGTG | 54455 |
rs780259418 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16332931 | AATGAGAAGAGTAGT[A/G]GCTTTTTCCAACAGA | 54455 |
rs780284083 | in-del | -/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16306714 | GTTTATTTATTTTTT[-/T]CTTTAGACAGGGTCT | 54455 |
rs780328481 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16326775 | CATCTAAAACACGTA[A/C]GCCAGAATCAACTAC | 54455 |
rs780342064 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16281241 | TGCTGGGATTACAGG[C/T]GTGAGCCGCAATGCC | 54455 |
rs780360857 | in-del | -/GTGG | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16254676 | TAAGGGAGGACAGGT[-/GTGG]GTGGGATGGTCTTGC | 54455 |
rs780412789 | snp | A/C | 1.85235e-05 | 0.00304326 | intron-variant | FBXO42 | GRCh38.p7 | 1:16255837 | CTAATGTAAAAAGAC[A/C]GGAGGAAGTCAAGAA | 54455 |
rs780418132 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16330339 | CAGCTGGGGCAACAC[A/G]GACTAGGCCCTGTTT | 54455 |
rs780424045 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16290114 | TAGCTGTGGGTCTCT[C/T]TTAGTGTAAGATCTG | 54455 |
rs780452580 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16254179 | CCTCATCTGAGCCAC[A/G]TCTGCGGCCAGACAC | 54455 |
rs780456256 | snp | A/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16268213 | TCTAGCCTGGTGTCA[A/C]AACAGAAAAATCCTT | 54455 |
rs780482451 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16300508 | ATGATATGCTTTTGC[A/G]TTTTCAGACGTCAAA | 54455 |
rs780501004 | snp | C/T | 1.65239e-05 | 0.00287431 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251211 | ACGTGAGGTGGGGTA[C/T]GCACACCATTTGTCT | 54455 |
rs780536388 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16311612 | GGGTAACACATAAGC[A/G]CATGAAAATACGCTC | 54455 |
rs780595619 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16326236 | AATTTTGTATTTTTT[C/T]GCAAAGACGGGGTTT | 54455 |
rs780617477 | snp | C/G | 1.72627e-05 | 0.00293786 | intron-variant | FBXO42 | GRCh38.p7 | 1:16315149 | AATCAATAAATAAAC[C/G]TTTCTCCTATCCACA | 54455 |
rs780628406 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16302900 | CCCCATGATCCAGTC[G/T]CCTCCCACCAGGTCA | 54455 |
rs780632457 | snp | A/G | 1.67312e-05 | 0.00289229 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251776 | TGAAGACCACCACAC[A/G]CTGTCCCACCTGGAA | 54455 |
rs780676776 | in-del | -/AAAAAATATAT | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16311498 | TCTCAAAAAAAAAAA[-/AAAAAATATAT]AAAAAATATATATAT | 54455 |
rs780676912 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16313679 | CAAGGACTCCATGAG[A/G]ACCACCTTGATGCAA | 54455 |
rs780729780 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16350670 | GAGAATCGCTTAAAC[C/T]CAGGGGATGGAGATT | 54455 |
rs780755995 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16297548 | CAAAATATTTATGGT[A/G]TCCCCAGAACTCTAC | 54455 |
rs780795697 | snp | A/G | 1.65018e-05 | 0.00287239 | synonymous-codon, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16252357 | CTTGAGTGGCTGCCA[A/G]GCCCAAGGACCAGAA | 54455 |
rs780881592 | snp | C/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16250803 | TGCAGGCTGGTTTCA[C/G]GAGGTCCAACCACAG | 54455 |
rs780883615 | snp | G/T | 1.70391e-05 | 0.00291878 | intron-variant | FBXO42 | GRCh38.p7 | 1:16253063 | GAACACTTAGTAGCA[G/T]GCACATGGGAATGCC | 54455 |
rs780896044 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16263637 | CTGAGGCAGGAGAAA[C/T]GCTTGAACCCGGGAG | 54455 |
rs780964544 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16261471 | TAGAATTTATCTCCA[C/T]GGCCTATTTTATGTC | 54455 |
rs780984566 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16268683 | AATAAGAACAAAGAG[A/G]CCGGGCACAGCAGCT | 54455 |
rs780984585 | snp | C/T | 3.29489e-05 | 0.00405874 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16315275 | CTCTTCTGGCAGCTC[C/T]GACATGGACCTATTA | 54455 |
rs781097008 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16342188 | GATCACTTGAAGCTG[A/G]GAGTTCAAGACCAGC | 54455 |
rs781104389 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16260736 | GGTCTCACTCTGGCA[C/T]CCAGGCTGGAGTGCA | 54455 |
rs781179887 | in-del | -/GAAG | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16332354 | TTGCTATAGTTGAAT[-/GAAG]GAAGATTAAATATAT | 54455 |
rs781263936 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16273659 | CTGAGGTGGGCAGAT[C/T]TCTTGAGCCTAGGAG | 54455 |
rs781274590 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16332688 | TGGGATTACAGACAT[G/T]TGCCACCATGCCCAG | 54455 |
rs781280015 | snp | C/T | 6.62482e-05 | 0.00575497 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251505 | GACAAACTCCCACCA[C/T]TGAGGATAGGAGAGC | 54455 |
rs781360070 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16313492 | TTGAGAAGTGAAACC[A/G]TGTATTTCCACATTG | 54455 |
rs781398936 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16346120 | TAGTGATACAGAAAG[C/T]AGCAAGGAAACTTAT | 54455 |
rs781410053 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16347177 | AAGCATCACAAGATA[C/T]ATCCACCTTTGAAGC | 54455 |
rs781449051 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16253889 | TTTAGAGATGCCCTA[C/T]TCAGAGTTCAGGGGC | 54455 |
rs781463138 | snp | A/C | 1.64841e-05 | 0.00287085 | missense, utr-variant-5-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16315394 | CCATGAAACTGTCAT[A/C]TTCACTGTCCGAGGA | 54455 |
rs781576346 | snp | A/C | | | intron-variant, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16253179 | AAGACATTGAAAATA[A/C]ACCTACAAAGACACA | 54455 |
rs781594371 | in-del | -/AAAC | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16285145 | CAAGACTCATCTCAA[-/AAAC]AAACAAACAAACAAA | 54455 |
rs781662385 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16338164 | CTCGGGAGGCTGAGG[C/G]AGGAGAATGGTGTGA | 54455 |
rs781691662 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16312283 | GGGAAGATGACTTGA[C/G]CCCGGGAGACGGAGG | 54455 |
rs781714125 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16338642 | AAAAACAGTGTTTCA[A/G]GAGGAATTCAAAGTA | 54455 |
rs781719911 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16305204 | AGCCTGGGCAATACA[C/G]TGAGACCCCATCTCT | 54455 |
rs781756251 | snp | G/T | 6.96706e-05 | 0.00590173 | intron-variant | FBXO42 | GRCh38.p7 | 1:16253766 | GGATAAAGGTAGTTA[G/T]GAGCTCCCAGGGACC | 54455 |
rs781757108 | snp | A/T | 1.65217e-05 | 0.00287412 | missense, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16251056 | TGCTCAAACTCTGGC[A/T]CCCAGGAGAGCCTGG | 54455 |
rs796142534 | in-del | -/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16269388 | CCACCGAACCCAGAC[-/T]TTTTTTTTTTTTTTA | 54455 |
rs796153578 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16252627 | CATGGAATTGTGCTT[G/T]TGACCCATGAATCAA | 54455 |
rs796154053 | in-del | AAGAGAAAAGAAAACAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16313310 | GAGAGAAAGAAAGAA[lengthTooLong]GAAAGAAAGAAAGAG | 54455 |
rs796170766 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16257280 | AGAAAAGGAGGCAGG[-/A]GGCAGTTCTTATTTG | 54455 |
rs796185642 | in-del | -/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16274562 | ATAAGTAATGTATAT[-/C]CCCCCCCCATACAAA | 54455 |
rs796210144 | multinucleotide-polymorphism | GT/TG | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16271267 | GTGTTGGTGTGTGTG[GT/TG]TGTGTGTGTGTGTGT | 54455 |
rs796230938 | in-del | -/TTC | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16279856 | GGTTTTTTTTTTCTT[-/TTC]TTTTTTTTGAGACAG | 54455 |
rs796232585 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16338376 | AAAAAAAAAAAAAAA[-/A]GAATAACAATGTTGC | 54455 |
rs796258937 | multinucleotide-polymorphism | GC/TA | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16293239 | ATTCTCCTGCCTCAG[GC/TA]TCCCAAGTAGGTGGG | 54455 |
rs796270299 | in-del | -/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16333437 | GGGCAAATAGTGAGA[-/C]CCCCCCCCCCCATTT | 54455 |
rs796365248 | snp | A/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16341609 | TGAGACTGCGTCTTT[A/T]AAAAAAAAAAAAAAA | 54455 |
rs796370058 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | FBXO42 | GRCh38.p7 | 1:16249899 | GAATAAATATGTTTT[C/T]TGGCAACTTGCCACC | 54455 |
rs796415397 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16324234 | ATATGTAAAAATACC[A/G]TGCTTATTGCAAGCT | 54455 |
rs796440566 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16264910 | TTTACGTTTGCAAAG[A/G]AGCTGGTTAAACAGT | 54455 |
rs796456814 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16261853 | GGACTACAGGCACCC[C/G]CCGCCATGCTCAAGC | 54455 |
rs796485216 | in-del | -/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16332546 | ATGAATTTCTTTTCC[-/T]TTTTTTTTTTTTTGA | 54455 |
rs796545079 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16350752 | AAACTGCAAAAAAAA[A/G]AAAAAAAAGAAAGAA | 54455 |
rs796617095 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16278358 | GCGAAACTCCATCTC[-/A]AAAAAAAAAACAAAA | 54455 |
rs796620986 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16334687 | CCATACAAAAGATAA[C/T]ACCAAGGTTGTTATG | 54455 |
rs796675487 | snp | G/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16274588 | ACAAATTATGCCCCC[G/T]TTTTTTTTTTTTTTT | 54455 |
rs796684604 | in-del | -/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16260226 | TTTTTTTTTTTTTTT[-/T]GAGACAGAATCTCAC | 54455 |
rs796719663 | in-del | -/AA | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16342398 | CGAAACTCTGTCTCA[-/AA]AAAAAAAAAAAAAAA | 54455 |
rs796738912 | snp | G/T | | | utr-variant-5-prime, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16352466 | TGCTGCTCAGGCCGG[G/T]AGAAGACAGCGCAGA | 54455 |
rs796788073 | snp | C/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16322851 | TATCAAGAAACTACT[C/G]TGAATTCATTGGAGA | 54455 |
rs796803334 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16299395 | ATTTTAATCCCACAC[C/T]AAAATAGGGCAATTG | 54455 |
rs796835478 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16307523 | TCTTAAAAAACAAGC[-/A]AAAAAAAAAAAAGAC | 54455 |
rs796864992 | in-del | -/TT | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16308495 | TGAGACCCATCTCTC[-/TT]TTTTTTTTTTTTTTT | 54455 |
rs796904204 | in-del | -/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16332545 | ATGAATTTCTTTTCC[-/T]TTTTTTTTTTTTTTG | 54455 |
rs796927102 | snp | A/G | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16300674 | TGAAGAAGCAAGGGC[A/G]GTTATCCAGTCTGGG | 54455 |
rs796929641 | in-del | -/A | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16290682 | GGGTGACAGAGTGAC[-/A]AAAAAAAAAAAAGAA | 54455 |
rs796963057 | snp | A/G | | | intron-variant, upstream-variant-2KB | FBXO42 | GRCh38.p7 | 1:16317687 | CCAACACTTTAGTAA[A/G]CCAAAACAGGAGGAT | 54455 |
rs796965752 | in-del | AA/C | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16296662 | TCAAAAAAAAAAAAA[AA/C]AAAACAAAAACAAAA | 54455 |
rs796986299 | snp | C/T | | | intron-variant | FBXO42 | GRCh38.p7 | 1:16328602 | ACATATAAATATTTA[C/T]AATTGGTGCATAATA | 54455 |