| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs201335951 | snp | C/G | | | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55162424 | AGGACATTAGCTAAT[C/G]TTCTCTCATCTAACT | 166979 |
| rs201340900 | snp | A/G | 0.000906223 | 0.0212671 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55161297 | TTTAAATTGCTTTTC[A/G]TTTTTAAACAATTAT | 166979 |
| rs201464892 | snp | G/T | 0.000548583 | 0.0165527 | intron-variant | CDC20B | GRCh38.p7 | 5:55128393 | ATACACAGAGAACAT[G/T]ATGAGAAAAAAAAAA | 166979 |
| rs201473174 | snp | C/T | 1.64866e-05 | 0.00287106 | missense, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160239 | GTTCCGGGCCCAGAG[C/T]AAAGGTATTTGCAGT | 166979 |
| rs201506312 | snp | C/G | 0.000230673 | 0.010737 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55146806 | TGCGGACAGCCTCTT[C/G]GCAAAGTTGCTCTTA | 166979 |
| rs201563549 | snp | A/G | 0.00210165 | 0.0323483 | intron-variant | CDC20B | GRCh38.p7 | 5:55124785 | ACAGGAAACCTAGAA[A/G]TCTATTGGGTTTCTT | 166979 |
| rs201729436 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55153618 | CCCCGGGGTGGACTG[A/G]AGGTTTAGTCTCTGG | 166979 |
| rs201760280 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CDC20B | GRCh38.p7 | 5:55120202 | TGGTCAAAGCAGTGA[C/T]GGGGAAAGAAAGGAA | 166979 |
| rs201881728 | snp | C/G | 0.000270517 | 0.0116269 | missense | CDC20B | GRCh38.p7 | 5:55128615 | AATCTAGGATATTCA[C/G]ATCTATAAGAAAAGC | 166979 |
| rs201898893 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55138182 | AAAAAAAAAAAAAAA[A/G]ACAGAGCTCACTCTG | 166979 |
| rs201959870 | snp | A/G | 1.66261e-05 | 0.00288319 | missense, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55161231 | CTAGGATCTGAAGGA[A/G]AACCTGCATTTAGAT | 166979 |
| rs202017113 | in-del | -/A | | | intron-variant | CDC20B | GRCh38.p7 | 5:55142304 | TCGCTTTGAGTCTTC[-/A]CCACTCTCGATGCTA | 166979 |
| rs202085105 | snp | A/G | 7.60138e-05 | 0.00616451 | intron-variant, upstream-variant-2KB | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170748 | ATTCAGGTCACTGCC[A/G]ATTCTCGTGGCCCAG | 166979 |
| rs202159957 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55142267 | ACATGAAGACACACG[C/T]TTACTCTACAGGGGA | 166979 |
| rs202220436 | snp | C/T | | | intron-variant, utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55137195 | AAAAAAAAAAAAAAA[C/T]AAAGAAAGCACTGAG | 166979 |
| rs202229164 | snp | G/T | 1.64849e-05 | 0.00287092 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55119904 | TGTCTTAGGTAGCCA[G/T]ATTAAGGAACAAATC | 166979 |
| rs267600653 | snp | A/G | 3.29663e-05 | 0.00405981 | CDC20B | 5 | allele_origin=G(germline)/A(somatic) | 5:55119821 | AACCCACCTGACCTG[A/G]ACACAGTGGGACAGG | 166979 |
| rs267600654 | snp | A/G | | | intron-variant, missense | CDC20B | GRCh38.p7 | 5:55120444 | GAGTTTGTGCTTGGG[A/G]TCTGGATGCTCTTCC | 166979 |
| rs267600655 | snp | A/G | | | stop-gained | CDC20B | GRCh38.p7 | 5:55128591 | TGGCAACAAGATTCT[A/G]AAAACTCCAATCTAG | 166979 |
| rs367571494 | in-del | C/TT | | | intron-variant | CDC20B | GRCh38.p7 | 5:55122284 | TTCTCTTTTTTTTTT[C/TT]TTAAGACACAGTCTC | 166979 |
| rs367578886 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55162118 | AAAAAAAAAAAGGCC[A/G]GGCGCGGTGGCTCAC | 166979 |
| rs367594319 | snp | C/T | 8.50897e-05 | 0.00652209 | intron-variant | CDC20B | GRCh38.p7 | 5:55128621 | GGATATTCAGATCTA[C/T]AAGAAAAGCACTTCA | 166979 |
| rs367682262 | snp | C/T | 1.64958e-05 | 0.00287187 | missense | CDC20B | GRCh38.p7 | 5:55128462 | CTGCCAGGCAAGTTC[C/T]CTCTTTTATCCAGGA | 166979 |
| rs367713693 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CDC20B | GRCh38.p7 | 5:55132377 | ATCATCTGACCTACG[C/G]GCTAGTCCATCCTCT | 166979 |
| rs367746464 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55122859 | ACACTTTTAGCTTCC[A/G]ATGCTGTCTGACTGC | 166979 |
| rs367876967 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55149352 | AATTACCACATGACC[A/G]AGCAAGTCCACTCAT | 166979 |
| rs367903017 | snp | C/T | 5.01953e-05 | 0.00500951 | missense | CDC20B | GRCh38.p7 | 5:55133423 | TTACAGTAGTCATTT[C/T]GAAGACCAGTAATAT | 166979 |
| rs367904963 | snp | A/T | 1.93827e-05 | 0.00311303 | intron-variant | CDC20B | GRCh38.p7 | 5:55146900 | CCACTGGCCTCAGTG[A/T]TGCAAAAGTAAAAAT | 166979 |
| rs367911795 | snp | G/T | 1.70664e-05 | 0.00292112 | splice-acceptor-variant, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164054 | GTTCTGGATATTTTA[G/T]ATTCTTCAAAGAAGG | 166979 |
| rs367928244 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55166524 | CTGTAACAATTAGGC[C/T]ATGTGTGCTGAGAGA | 166979 |
| rs367942807 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55154509 | GTGACAGAGTGAGAC[C/T]GTGTCTCCCAAGAAA | 166979 |
| rs368052511 | snp | A/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55138165 | AAATAGATTTTGAGT[A/T]AAAAAAAAAAAAAAA | 166979 |
| rs368112512 | snp | C/T | 1.71908e-05 | 0.00293174 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55161283 | CTTGCATATGCTGTT[C/T]TAAATTGCTTTTCAT | 166979 |
| rs368120952 | in-del | -/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55147424 | GTTATATTTTATATA[-/T]TTTTTATATTGATAT | 166979 |
| rs368129667 | snp | A/G | 1.9255e-05 | 0.00310276 | intron-variant | CDC20B | GRCh38.p7 | 5:55128385 | GTGTAATAATACACA[A/G]AGAACATGATGAGAA | 166979 |
| rs368194274 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55122339 | CAGTGCTACCACAAA[A/G]GGTCAATGAAGCCTC | 166979 |
| rs368209113 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | CDC20B, MIR449A | GRCh38.p7 | 5:55170068 | GCAGTGAGCCGAGAT[C/G]GCGCCACTGTACTCC | 166979 |
| rs368393866 | snp | G/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55153044 | AGGAGTTCAAGACCA[G/T]CCTCGACAATGTGGC | 166979 |
| rs368590133 | snp | A/G | | | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55158844 | TAGGCCCCCTGTGCC[A/G]GGCAACAGCCAGGGG | 166979 |
| rs368669273 | snp | C/T | 1.64749e-05 | 0.00287005 | missense | CDC20B | GRCh38.p7 | 5:55146709 | TGGTTGACTGCTCTT[C/T]CCCAAAGGAATCAGA | 166979 |
| rs368673539 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55155133 | AAGGGATGAATGACT[C/T]GGTACTCCAAGCACA | 166979 |
| rs368793245 | snp | A/C/G | 0.000141857 | 0.00842092 | intron-variant, upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55172889 | ATGAACGGGGCCTTC[A/C/G]GCCCCGCATTAGAGA | 166979 |
| rs368807177 | snp | A/G | 6.64927e-05 | 0.00576558 | intron-variant | CDC20B | GRCh38.p7 | 5:55140310 | CAATGTCTTGATCCT[A/G]TACCTTTCCAAACAC | 166979 |
| rs368819650 | snp | A/G | 1.64972e-05 | 0.00287199 | missense | CDC20B | GRCh38.p7 | 5:55124991 | GATGCTGGGCTACCC[A/G]AACATCGTGATGATA | 166979 |
| rs368828314 | snp | C/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55141127 | CAGAAAGAACACTTT[C/G]GGGGGCCGTAGGCAG | 166979 |
| rs368837391 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55169464 | GCATGTCTGGAAGCC[A/C]GCACATATCTATGCT | 166979 |
| rs368903816 | snp | A/C | 7.06277e-05 | 0.00594213 | intron-variant | CDC20B | GRCh38.p7 | 5:55140426 | AAAATAAACACACAT[A/C]AGGAGAATATTTCTT | 166979 |
| rs368918101 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55139038 | AATATCCACCAATGG[A/G]CTTTTGATTTACAAT | 166979 |
| rs368934577 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55115817 | CATATTTGAGATGCT[C/T]ATTCTTCTACACACA | 166979 |
| rs368953933 | snp | A/G | 0.000153988 | 0.00877328 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164141 | TTCTGGAAGCCAGAG[A/G]AGCCCATTGAAGTCA | 166979 |
| rs369037343 | snp | C/T | 3.31719e-05 | 0.00407245 | intron-variant | CDC20B | GRCh38.p7 | 5:55114355 | GTTCATACTCCTCCA[C/T]GTTACATGGGCTGCT | 166979 |
| rs369105679 | snp | A/C | 1.64773e-05 | 0.00287026 | intron-variant, upstream-variant-2KB | CDC20B, MIR449A, MIR449B, MIR449C | GRCh38.p7 | 5:55172542 | AAGAATTCGTTTGTT[A/C]AAGATCAGAATTAAA | 166979 |
| rs369106085 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55114233 | CTAGTAGCAATTCCA[C/T]ACAGAGGCCGTCCCA | 166979 |
| rs369308285 | snp | G/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55118687 | GACTCATGCTCTTCC[G/T]ACACTTGCACCTGAT | 166979 |
| rs369372041 | snp | A/G | 3.3534e-05 | 0.00409461 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160401 | ATAAAGGCAAAGTAA[A/G]TTGCATCATCTGATT | 166979 |
| rs369386172 | in-del | -/GA | | | intron-variant | CDC20B | GRCh38.p7 | 5:55135755 | CTGAGATTTTTTTGT[-/GA]TTTTTTTTTTTTTTT | 166979 |
| rs369436795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55136540 | CTCCAGCCTGGACGA[C/T]AGAGCAAGACTTCAT | 166979 |
| rs369497492 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55128201 | TTTTTAAATATGACA[C/G]AAAGATTGTGGTGGA | 166979 |
| rs369502428 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CDC20B | GRCh38.p7 | 5:55133290 | AGCCATATTTGGATG[C/T]TACACTATTTGGATA | 166979 |
| rs369569862 | snp | A/G | 8.27164e-05 | 0.0064305 | intron-variant, nc-transcript-variant, downstream-variant-500B | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170622 | AGCTCATCACACACA[A/G]GTATCCAGAGCACTT | 166979 |
| rs369630438 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55154101 | GACAAGTCAGGATTC[A/G]AACCCTGAGTTCATT | 166979 |
| rs369634951 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55129989 | ATAGATGAAAACTCC[A/C]AGGTGACCTAGGTAT | 166979 |
| rs369665527 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55139948 | ATGAGAGTCCTTTGA[A/G]CCCGGGAGGCAAAGG | 166979 |
| rs369767237 | snp | A/C | 0.000153988 | 0.00877328 | missense, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160259 | GTATTTGCAGTTTTG[A/C]TGTCTATAGTTCTAT | 166979 |
| rs369841777 | snp | A/G/T | 1.754e-05 | 0.00296137 | stop-gained, synonymous-codon | CDC20B | GRCh38.p7 | 5:55114224 | GGCTGGGTGCTAGTA[A/G/T]CAATTCCATACAGAG | 166979 |
| rs369914211 | in-del | -/AA | | | intron-variant | CDC20B | GRCh38.p7 | 5:55138858 | CCCAAAAGGTTTAAA[-/AA]TAAAAAAGTGAGATG | 166979 |
| rs369948168 | snp | A/G | 0.000132035 | 0.00812404 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55124998 | GGCTACCCGAACATC[A/G]TGATGATAAACACGC | 166979 |
| rs370192875 | snp | A/C | 0.000292783 | 0.0120957 | intron-variant, upstream-variant-2KB, nc-transcript-variant | CDC20B, MIR449A, MIR449B, MIR449C | GRCh38.p7 | 5:55172270 | GGGGCGTGCTTCTGA[A/C]TGCAACAGAGAGGAG | 166979 |
| rs370277291 | snp | A/C | 0.000181236 | 0.00951761 | intron-variant, missense | CDC20B | GRCh38.p7 | 5:55120438 | ACCTGTGAGTTTGTG[A/C]TTGGGGTCTGGATGC | 166979 |
| rs370294226 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55115393 | GCATTACAAATGTTT[C/T]GGAGATGAGGCAACA | 166979 |
| rs370294376 | snp | G/T | | | intron-variant, downstream-variant-500B | CDC20B | GRCh38.p7 | 5:55136347 | GGCAGATCATTTGTG[G/T]CCAGAGTTCAAGACC | 166979 |
| rs370363882 | snp | C/G | 0.000153988 | 0.00877328 | utr-variant-5-prime, upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55173022 | CTGACTTCGCCCTGC[C/G]TGGCGTTTGGCCTCT | 166979 |
| rs370409177 | snp | A/C/G/T | 4.94601e-05 | 0.00497275 | missense, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160236 | AATGTTCCGGGCCCA[A/C/G/T]AGCAAAGGTATTTGC | 166979 |
| rs370497969 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55131862 | TTGAGGTCAGGAGTT[C/T]GAGACTAGCCTGGCC | 166979 |
| rs370541942 | snp | C/G | | | upstream-variant-2KB | CDC20B | GRCh38.p7 | 5:55175116 | AAAATAAAATCACAA[C/G]TTTTCACTGGCCAAA | 166979 |
| rs370579564 | in-del | -/GGAGG | | | intron-variant | CDC20B | GRCh38.p7 | 5:55126278 | GCCGAGGCAGGTGGA[-/GGAGG]TCACAAGGTCAGGAG | 166979 |
| rs370579774 | snp | A/T | 1.72728e-05 | 0.00293872 | intron-variant | CDC20B | GRCh38.p7 | 5:55143676 | ATCTTTGAATTTGGT[A/T]TTTAAAACAAGATAA | 166979 |
| rs370604635 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | CDC20B | GRCh38.p7 | 5:55114532 | CAGTGCTCTTGCCCC[A/T]GTATCAGTGTCCTGT | 166979 |
| rs370607045 | snp | C/T | | | intron-variant, downstream-variant-500B | CDC20B | GRCh38.p7 | 5:55136052 | TGGTTCAAGCAATTC[C/T]CCTGCCTCAGCCTCC | 166979 |
| rs370744513 | snp | G/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55130783 | AATACTTTTTAAATT[G/T]TAAAACGTTTACAAT | 166979 |
| rs370821763 | snp | C/G | 3.29571e-05 | 0.00405924 | missense | CDC20B | GRCh38.p7 | 5:55146672 | GTCTTCAGCACTGAT[C/G]CGGAAGCTTCTGGGA | 166979 |
| rs370856727 | snp | A/G | 1.65086e-05 | 0.00287298 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55127259 | AGACGCTTCTTACCT[A/G]CTGAGGATAAAGTGA | 166979 |
| rs370876326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55114496 | ACAGCAGTCAGGGCC[A/G]ACTGGGACAGTTTTC | 166979 |
| rs370900103 | in-del | -/A | 0.296109 | 0.245711 | intron-variant | CDC20B | GRCh38.p7 | 5:55138732 | TGAACAGGATGCTGT[-/A]AAAAAAAAAAAAAGG | 166979 |
| rs370941496 | snp | C/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55131216 | GGGGACTTTGAGAGA[C/G]CTATGTGATTGCAAG | 166979 |
| rs371047336 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55121896 | CACCTACATCTTAAC[A/G]CTTTTCTTACAAGTT | 166979 |
| rs371064778 | snp | C/G | 0.000153988 | 0.00877328 | missense, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55161160 | GCAAGGAAGTAGAAT[C/G]TTTTGCAAGAAAAAA | 166979 |
| rs371099810 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CDC20B | GRCh38.p7 | 5:55141648 | CCCCACGGTTCAGAC[A/G]GAAGTCTCTCTGACA | 166979 |
| rs371124391 | in-del | -/AT | | | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55162231 | TGAAACCCCATCTCT[-/AT]TAATAGTACAAAAAT | 166979 |
| rs371178558 | in-del | -/A | | | intron-variant | CDC20B | GRCh38.p7 | 5:55138010 | CCACACATACACACA[-/A]CACCCTGCCCAACCA | 166979 |
| rs371195518 | snp | C/G | 0.000153988 | 0.00877328 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55114302 | CAAAGACAGGTGCAG[C/G]ACTCTGCCCCTGTGG | 166979 |
| rs371200410 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55132410 | CAACTACCAGCATTC[A/G]TTTCAAATAATCTGC | 166979 |
| rs371294393 | snp | C/T | 1.65007e-05 | 0.00287229 | missense | CDC20B | GRCh38.p7 | 5:55146831 | CTCTTAAAGTCAGAA[C/T]ACGTAGCATTAACTG | 166979 |
| rs371314228 | snp | A/T | | | upstream-variant-2KB | CDC20B | GRCh38.p7 | 5:55174931 | TAGAGAAAGTATTAG[A/T]CAAATATCTTTAGGA | 166979 |
| rs371333285 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, downstream-variant-500B | CDC20B | GRCh38.p7 | 5:55136318 | TAATCCCAGCACTTT[A/G]GGAGGCCAAGGTGGG | 166979 |
| rs371465617 | snp | C/T | 1.65987e-05 | 0.00288082 | intron-variant | CDC20B | GRCh38.p7 | 5:55127396 | GCATTGGAGTTTTCA[C/T]AGCCCACTGTCTTCT | 166979 |
| rs371465951 | snp | C/T | 4.9807e-05 | 0.00499009 | intron-variant, upstream-variant-2KB, nc-transcript-variant | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170681 | AAGTGGCAGGGTAGT[C/T]GTGGCTGCTGACTTG | 166979 |
| rs371562932 | snp | C/T | | | intron-variant, utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55136537 | GCACTCCAGCCTGGA[C/T]GATAGAGCAAGACTT | 166979 |
| rs371708882 | in-del | -/G | | | intron-variant, utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55137113 | ACCCGGGAGACAGAG[-/G]TTGCAGTGAACTGAG | 166979 |
| rs371779986 | snp | A/G | 0.000469529 | 0.0153148 | intron-variant, upstream-variant-2KB | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170755 | TCACTGCCGATTCTC[A/G]TGGCCCAGGCAGTCA | 166979 |
| rs371857205 | snp | C/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55166283 | TCAACATGATACAGA[C/T]GAACATCCTGCCTTA | 166979 |
| rs371884127 | snp | C/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55150457 | GGGGCGAGGCCGGCT[C/G]TCTCTCCACTGCTGC | 166979 |
| rs371977675 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55153026 | GGTGGATGGCTTGAG[C/T]TCAGGAGTTCAAGAC | 166979 |
| rs372002291 | snp | A/T | 6.73401e-05 | 0.0058022 | intron-variant | CDC20B | GRCh38.p7 | 5:55133537 | TTGCAGCCTACAAGA[A/T]ACAAACACTTCTACA | 166979 |
| rs372025135 | snp | C/T | 1.72868e-05 | 0.00293992 | intron-variant | CDC20B | GRCh38.p7 | 5:55124790 | AAACCTAGAAATCTA[C/T]TGGGTTTCTTACCTT | 166979 |
| rs372084834 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55132926 | ATAAATATCTCCACA[A/C]CGTCTTTCTGGACAA | 166979 |
| rs372136370 | snp | C/T | | | downstream-variant-500B | CDC20B | GRCh38.p7 | 5:55112626 | TTTCTAAGGCAAGAA[C/T]TACTAACATTACCAA | 166979 |
| rs372138279 | snp | C/T | | | intron-variant, downstream-variant-500B | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170162 | AAGAATCCTAAAGAC[C/T]TCACTGAAAATCTGG | 166979 |
| rs372181403 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | CDC20B | GRCh38.p7 | 5:55143818 | GCCCAGGCTCTCGTC[A/G/T]CTCCAAAGTCCATTG | 166979 |
| rs372227357 | snp | C/G | 6.16073e-05 | 0.00554976 | utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55114207 | AAACTGAAACCTAGA[C/G]GGGCTGGGTGCTAGT | 166979 |
| rs372229219 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55152339 | CTGTGCTTCCACACT[A/C]ACTGTGCATGCTCCA | 166979 |
| rs372251442 | snp | A/G | | | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55162124 | AAAAAGGCCGGGCGC[A/G]GTGGCTCACGCCTGT | 166979 |
| rs372270269 | in-del | -/A | 0.00517822 | 0.0506191 | intron-variant | CDC20B | GRCh38.p7 | 5:55147580 | TATGTGTAAAATGTT[-/A]TTTTTTTATGTTTAT | 166979 |
| rs372292804 | snp | A/C | 0.000153988 | 0.00877328 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164172 | TCAGGCCTGACATAG[A/C]AGCTCTGGTTAGACA | 166979 |
| rs372295677 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55129247 | CTACAGTAGTTTAAA[A/C]CCCTACAATACATTC | 166979 |
| rs372312032 | snp | C/G/T | | | utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55113083 | TCATTTCAAAACACT[C/G/T]CCTGGAGAGGTTAGG | 166979 |
| rs372325740 | snp | C/T | 1.64792e-05 | 0.00287042 | missense | CDC20B | GRCh38.p7 | 5:55124880 | CGTGGGGCCATATTG[C/T]CAGCAGTCCATCACT | 166979 |
| rs372327112 | snp | A/G | | | intron-variant, upstream-variant-2KB | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55171198 | GCTGCCTGTAATCCC[A/G]GCTACTCAGGAGGCT | 166979 |
| rs372330536 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CDC20B | GRCh38.p7 | 5:55143023 | AATAAATAAAAGATA[C/T]CTAAATGTAATAAAT | 166979 |
| rs372340296 | snp | C/T | | | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55162960 | ACCACTCATTAGCCA[C/T]GTGACCTTGTGTCTA | 166979 |
| rs372361181 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55166155 | TGTTTTATGCATTCA[C/T]GTTAGGAGCATGAGC | 166979 |
| rs372402086 | snp | A/G | 3.32962e-05 | 0.00408007 | missense | CDC20B | GRCh38.p7 | 5:55114243 | TTCCATACAGAGGCC[A/G]TCCCATCAGCTGCAG | 166979 |
| rs372418939 | snp | A/G | 1.96242e-05 | 0.00313237 | intron-variant | CDC20B | GRCh38.p7 | 5:55146902 | ACTGGCCTCAGTGAT[A/G]CAAAAGTAAAAATTC | 166979 |
| rs372419923 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55130373 | AGAATGAAGCCTCAG[C/T]GAATTGTGGAATAAT | 166979 |
| rs372542756 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55147517 | TATATAAAAATGTTA[C/T]GTATTTTTATATATT | 166979 |
| rs372543151 | snp | A/T | 3.46915e-05 | 0.00416468 | intron-variant | CDC20B | GRCh38.p7 | 5:55146581 | TCTCAGGAATATATC[A/T]TTTATTCACGTTGCA | 166979 |
| rs372598291 | snp | A/G | | | utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55113944 | TCTGAATAAAGTAGT[A/G]AAAATGAATCTCTAG | 166979 |
| rs372719335 | snp | A/C | 0.000155988 | 0.00883004 | intron-variant, upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55172891 | GAACGGGGCCTTCGG[A/C]CCCGCATTAGAGAGT | 166979 |
| rs372774365 | snp | C/T | 1.65798e-05 | 0.00287917 | missense | CDC20B | GRCh38.p7 | 5:55140386 | CCACGTTCTGGGTTA[C/T]AAAGAGTTGTTTTAG | 166979 |
| rs372780864 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55141079 | AACTACGCCAAAGGT[C/T]ATGTTGAGGTCTGGA | 166979 |
| rs372856760 | in-del | -/A | 0.4941 | 0.0539917 | intron-variant | CDC20B | GRCh38.p7 | 5:55128261 | TAAAAACCATTCAGT[-/A]AAAAAAAAAAAAAAA | 166979 |
| rs372884755 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55125096 | AAAACATGGAGGAAA[G/T]CATAGTTCAAAGTAA | 166979 |
| rs373013418 | snp | A/G | 8.25921e-05 | 0.00642567 | synonymous-codon, intron-variant, nc-transcript-variant, splice-acceptor-variant | GPX8, CDC20B | GRCh38.p7 | 5:55161050 | AGACAGAAATTACTT[A/G]GGGCTGAAGGAACTG | 166979 |
| rs373014288 | snp | A/G | | | upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55173780 | TTCCCTGCTCTATAC[A/G]TTGGGAGTAGTCAGG | 166979 |
| rs373102985 | snp | C/T | 1.64836e-05 | 0.0028708 | missense, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160302 | TATTTCTTCTACAAC[C/T]AAAATTCCTCAAACC | 166979 |
| rs373113263 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55150760 | TTGTTTTGCTTTGTT[A/G]TTTTGAGGCAGTCTC | 166979 |
| rs373126850 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55119362 | TTGTAGAACGAAGCT[C/G]AGAAGAGTAGTGGTC | 166979 |
| rs373219634 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55134282 | ACCAGATGGCTTCTG[A/C]TAAAAGCATGAGAGC | 166979 |
| rs373225098 | snp | A/G | | | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55161624 | ACACAGCTCTCATGA[A/G]TAGTGCTGGGCATTA | 166979 |
| rs373234118 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55123598 | CAGGTGCTGACTGCC[A/G]GGAGGCTTGGCTTGC | 166979 |
| rs373243354 | snp | C/T | 0.000165862 | 0.00910514 | intron-variant | CDC20B | GRCh38.p7 | 5:55119774 | TTTGCTATAGGTGCA[C/T]GGCATTTTACTCACC | 166979 |
| rs373258746 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55121174 | AGGACATTTTAACAA[A/G]TACTACAGTTATATG | 166979 |
| rs373275209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55168860 | AGGACTGAAAAACTA[C/T]CTATTGGGTACAATG | 166979 |
| rs373321917 | snp | A/T | | | intron-variant, upstream-variant-2KB | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55171220 | CAGGAGGCTGAGACA[A/T]GAGAATCACTTGAAC | 166979 |
| rs373327373 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55144222 | AGATGTTTTAAAGAT[A/G]GTTTAAGATGGCATC | 166979 |
| rs373378995 | snp | A/G | 2.26601e-05 | 0.00336594 | missense, upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55172970 | CCGTGCGGACCCTCC[A/G]AGGCGCGGTGCGCTC | 166979 |
| rs373420526 | snp | C/T | 9.89887e-05 | 0.00703452 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164148 | AGCCAGAGGAGCCCA[C/T]TGAAGTCATCAGGCC | 166979 |
| rs373422364 | snp | A/G | 1.65119e-05 | 0.00287327 | missense | CDC20B | GRCh38.p7 | 5:55143553 | TTCCAGTCTCTGTCC[A/G]TTGCATGAGGTGCCT | 166979 |
| rs373491856 | snp | G/T | 0.000193981 | 0.00984647 | intron-variant, upstream-variant-2KB, downstream-variant-500B | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170637 | GGTATCCAGAGCACT[G/T]CATTGACAAGAAGAA | 166979 |
| rs373515157 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164676 | ATGACTGAAATTTCT[A/G]GAATAACTGTAAATG | 166979 |
| rs373550396 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55130576 | GCAAAAATCTCATCA[A/G]CTGGAAGATGGAAAA | 166979 |
| rs373577998 | in-del | -/AT | | | intron-variant | CDC20B | GRCh38.p7 | 5:55145984 | GCAAAACAAAAGCAC[-/AT]ATATATATGTGTGTA | 166979 |
| rs373694749 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55151050 | CTCACAGGGCCACTC[A/G]AACTTTCATTTCCCC | 166979 |
| rs373740107 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, upstream-variant-2KB | CDC20B, MIR449B, MIR449C | GRCh38.p7 | 5:55172627 | CTGCTTCAAGTCTTT[A/G]GAGAGCACACGCATG | 166979 |
| rs373745432 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | CDC20B | GRCh38.p7 | 5:55138954 | AAAATAAATGACAAT[A/G]AAAAAAATATTAAAA | 166979 |
| rs373822687 | snp | C/G | 0.000153988 | 0.00877328 | missense | CDC20B | GRCh38.p7 | 5:55146717 | TGCTCTTCCCCAAAG[C/G]AATCAGAGGACAGAG | 166979 |
| rs373960357 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CDC20B | GRCh38.p7 | 5:55130072 | AAAACACACATGAAA[C/T]GAATGAAAATTTATA | 166979 |
| rs374037754 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55114552 | CAGTGTCCTGTGGCT[A/G]CCATAACAAATTACC | 166979 |
| rs374125586 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant, missense | CDC20B | GRCh38.p7 | 5:55120481 | TTATATCCAAGATGT[A/G]TAAGCGTCCATCCTT | 166979 |
| rs374153257 | snp | A/G | 3.29587e-05 | 0.00405934 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55146674 | CTTCAGCACTGATCC[A/G]GAAGCTTCTGGGAGG | 166979 |
| rs374165318 | snp | G/T | 0.000165306 | 0.00908986 | missense, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164093 | TGGAATTTTTGGAAG[G/T]ATCTTGTCAACCCTG | 166979 |
| rs374185198 | in-del | -/G | | | intron-variant, utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55137195 | AAAAAAAAAAAAAAA[-/G]AAAGAAAGCACTGAG | 166979 |
| rs374320134 | snp | C/T | 0.000357681 | 0.0133683 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55161272 | AGCTTCATAAAACT[C/T] | 166979 |
| rs374341417 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55142669 | GGACTCCCCGGCCAT[C/T]CCCTATCCCCCAAAC | 166979 |
| rs374422547 | snp | A/G | | | intron-variant, utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55137164 | CTTGGGCAACAGAGC[A/G]AGACTCTGTCTCAAA | 166979 |
| rs374482641 | snp | G/T | 0.000167108 | 0.00913925 | intron-variant, upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55172916 | GAGAGTTAGGGAGAA[G/T]GCAGAAAAGGGTGTT | 166979 |
| rs374511741 | snp | C/T | 1.66432e-05 | 0.00288467 | missense, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55161235 | GATCTGAAGGAGAAC[C/T]TGCATTTAGATTTCT | 166979 |
| rs374544307 | snp | A/T | 1.6483e-05 | 0.00287076 | intron-variant | CDC20B | GRCh38.p7 | 5:55120387 | TCACAAGATTCCAGA[A/T]GATCAAAATGAAGAT | 166979 |
| rs374619191 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55113106 | AGGTTAGGACTTGTG[C/T]GGGTGTGTAAAGGAA | 166979 |
| rs374772594 | in-del | -/CT | 0.00478085 | 0.0486577 | intron-variant | CDC20B | GRCh38.p7 | 5:55123343 | GGCTCAGAAATTCCC[-/CT]GAGCCCATGGGCCCC | 166979 |
| rs374792016 | snp | C/T | 1.66682e-05 | 0.00288684 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55140396 | GGTTACAAAGAGTTG[C/T]TTTAGGCATTTCTGA | 166979 |
| rs374800679 | snp | C/G/T | 0.000153988 | 0.00877328 | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164230 | ATGAGAATGCCATTG[C/G/T]GTTTCTAATAGAACA | 166979 |
| rs374883017 | snp | A/G | 3.31356e-05 | 0.00407022 | intron-variant, nc-transcript-variant, downstream-variant-500B | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170556 | AATAAGACAGCAGTT[A/G]CATGTTAGCCGATGC | 166979 |
| rs374910860 | snp | A/G | 5.00705e-05 | 0.00500327 | splice-donor-variant, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160397 | AAGTATAAAGGCAAA[A/G]TAAGTTGCATCATCT | 166979 |
| rs374983644 | snp | C/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55117878 | CCAGCACTTTGGGAG[C/G]CCGAGGTGGGTGGAT | 166979 |
| rs375000137 | snp | A/T | 3.31934e-05 | 0.00407377 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55128430 | CAGTACTTGCACTTC[A/T]CCCTCGCTGGTGCCA | 166979 |
| rs375001817 | snp | C/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55166682 | TTCTGCATCAAAAAG[C/T]CTGGGACACAGAGTG | 166979 |
| rs375088806 | snp | A/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55131226 | AGAGACCTATGTGAT[A/T]GCAAGATGTTTATAT | 166979 |
| rs375116100 | in-del | -/A | | | intron-variant, upstream-variant-2KB | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55171193 | GTGGTGCTGCCTGTA[-/A]TCCCAGCTACTCAGG | 166979 |
| rs375289355 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55129456 | TTGATGGAGTGCCAG[C/T]GAAGACTCTGACAAA | 166979 |
| rs375307186 | snp | G/T | 0.000153988 | 0.00877328 | missense, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55161244 | GAGAACCTGCATTTA[G/T]ATTTCTTGTTGGTAA | 166979 |
| rs375314617 | snp | A/G/T | 5.34872e-05 | 0.00517119 | stop-gained, synonymous-codon | CDC20B | GRCh38.p7 | 5:55114221 | AGGGGCTGGGTGCTA[A/G/T]TAGCAATTCCATACA | 166979 |
| rs375447069 | snp | C/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55116219 | CATATAAATGAAAAG[C/G]AACTTGATTTAGTTG | 166979 |
| rs375475047 | snp | C/T | 0.000131922 | 0.00812056 | synonymous-codon, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160217 | CTTGCAGCTTACCCG[C/T]TAAAATGTTCCGGGC | 166979 |
| rs375559947 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55123492 | CATGAGAGGAATCAC[A/G]CACATGTCAACCTGC | 166979 |
| rs375564306 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55143905 | TGAGAAAGCTGTCTC[A/C/G]GTGGCCTCTAGAGCA | 166979 |
| rs375620575 | in-del | -/A | | | intron-variant | CDC20B | GRCh38.p7 | 5:55117304 | GGTACGGCTTAGTAA[-/A]GGTGTGACCAGAATC | 166979 |
| rs375649984 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55142238 | AAACACCCTCCAGAT[A/G]ATCAGTGAGGACCAC | 166979 |
| rs375653898 | in-del | -/CTCTTT | | | intron-variant | CDC20B | GRCh38.p7 | 5:55145776 | CTCTCTTCTCTCTTT[-/CTCTTT]GTCTCTCTCCCCCCA | 166979 |
| rs375754379 | in-del | -/C | | | intron-variant, utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55137520 | TTCATAGTTTAAGTT[-/C]CCTTAAAAGAATCAA | 166979 |
| rs375811168 | snp | A/G | 0.000468212 | 0.0152934 | intron-variant, downstream-variant-500B | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170530 | TACACTCTGATGTTC[A/G]TTGTATATGCAATAA | 166979 |
| rs375895997 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55138667 | TACTTCTAAAAATCT[A/G]TAAAATAATATTGTC | 166979 |
| rs375917242 | snp | C/T | 0.000148271 | 0.00860893 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55124923 | AAGCAGCCTGCCATC[C/T]GGTGACCACTTCAGA | 166979 |
| rs375938676 | snp | C/T | 3.31104e-05 | 0.00406867 | intron-variant | CDC20B | GRCh38.p7 | 5:55114345 | AGGAAAGACAGTTCA[C/T]ACTCCTCCACGTTAC | 166979 |
| rs375941431 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | CDC20B | GRCh38.p7 | 5:55114617 | TCTCACAGTTCTGGA[A/G]ATGGGAAGTCTGAAA | 166979 |
| rs375954474 | snp | A/G | | | intron-variant, downstream-variant-500B | CDC20B | GRCh38.p7 | 5:55136211 | TCGGCCTCCCAAAGT[A/G]CTGGGATTATAGGCG | 166979 |
| rs375974385 | snp | C/T | 6.63956e-05 | 0.00576137 | intron-variant | CDC20B | GRCh38.p7 | 5:55114362 | CTCCTCCACGTTACA[C/T]GGGCTGCTGCTCAGG | 166979 |
| rs375990543 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CDC20B | GRCh38.p7 | 5:55126587 | ATATATTTAGACCAG[C/T]TATGTAGGCTCATAG | 166979 |
| rs376019773 | snp | A/G | | | upstream-variant-2KB | CDC20B | GRCh38.p7 | 5:55175068 | AATTACCTTGCATAT[A/G]ATGAGAATACTTCCC | 166979 |
| rs376049119 | snp | A/C | | | intron-variant, utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55136582 | AAAAAAAAAATAGGA[A/C]AAGCCATAAAAATAG | 166979 |
| rs376052285 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55119659 | ACGCTCTCTGAGGTA[A/G]GGTGGATGTAGGACT | 166979 |
| rs376056218 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55140770 | TGGCCATCTTAAGGT[A/C]CTTTTTTGTTAACAC | 166979 |
| rs376078873 | snp | G/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55151108 | AAAACCGCAGTACCA[G/T]CTCAGAGGCTTTGGG | 166979 |
| rs376114328 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55142305 | CGCTTTGAGTCTTCA[A/C]CACTCTCGATGCTAT | 166979 |
| rs376118626 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164764 | TTCAAATCCTTATAT[A/G]TGTATGCTTGTTTTG | 166979 |
| rs376152229 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55114673 | CCTAGGGAGGCTCTC[C/G]AGGGGATTCCATGCT | 166979 |
| rs376160250 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55135046 | ACTATGGACTTTTGG[C/T]GACCATGATGTGTCA | 166979 |
| rs376179606 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55169107 | GAAAATAACATGTTG[A/C]AATTTAACCTTAAAA | 166979 |
| rs376203465 | snp | A/G | 0.000142952 | 0.00845313 | intron-variant | CDC20B | GRCh38.p7 | 5:55146887 | AACAGCTGTAAGTCC[A/G]CTGGCCTCAGTGATG | 166979 |
| rs376208327 | snp | A/C | 4.94303e-05 | 0.00497119 | missense | CDC20B | GRCh38.p7 | 5:55119856 | CACAGTCACATCATT[A/C]TTGGGAGTACCTTGA | 166979 |
| rs376326185 | snp | C/T | 1.66835e-05 | 0.00288816 | intron-variant | CDC20B | GRCh38.p7 | 5:55140302 | AAGAAGGACAATGTC[C/T]TGATCCTGTACCTTT | 166979 |
| rs376348137 | in-del | -/TC | | | intron-variant | CDC20B | GRCh38.p7 | 5:55126277 | GGCCGAGGCAGGTGG[-/TC]ATCACAAGGTCAGGA | 166979 |
| rs376352678 | in-del | -/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55120968 | TGTTCCAGGTAGTGG[-/G]TCAGATAAGAGAAAA | 166979 |
| rs376526698 | snp | A/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55132992 | GCTCCTTATATCCCA[A/T]GATTTATTATTTATA | 166979 |
| rs376696799 | snp | A/G | | | intron-variant, downstream-variant-500B | GPX8, CDC20B | GRCh38.p7 | 5:55167345 | ATGTTTAACAATTAC[A/G]CTGTATCAATAGTAT | 166979 |
| rs376727809 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CDC20B | GRCh38.p7 | 5:55133955 | AATATTTATTGATTC[A/G]TTGATTTTAGCTCTT | 166979 |
| rs376735655 | snp | A/G | 1.64738e-05 | 0.00286995 | missense, upstream-variant-2KB | CDC20B, MIR449B, MIR449C | GRCh38.p7 | 5:55172632 | TCAAGTCTTTGGAGA[A/G]CACACGCATGATACT | 166979 |
| rs376793999 | snp | A/G | | | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55162339 | GGCAGAGGTTGCAGT[A/G]AGCTGAAATCGCGCT | 166979 |
| rs376857872 | in-del | -/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55138599 | AAAGTAAATGGGGGG[-/G]TTGGAGGGAGAGAAA | 166979 |
| rs377005254 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55147884 | TTCATTTCACAGATG[A/G]GGAAGCTGAGGCCTA | 166979 |
| rs377067494 | snp | A/C | 0.000193981 | 0.00984647 | intron-variant, upstream-variant-2KB, nc-transcript-variant | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170658 | ACAAGAAGAATTTAT[A/C]CAGAAGCAAGTGGCA | 166979 |
| rs377089008 | snp | A/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55150160 | AAAAAATTAAAAAAT[A/T]AAGGTTTTTTTAAAT | 166979 |
| rs377118253 | snp | A/G | 5.09992e-05 | 0.00504945 | intron-variant | CDC20B | GRCh38.p7 | 5:55140277 | GAGGCAGAGAGAGAG[A/G]AGCGCAGGAAAGAAG | 166979 |
| rs377125378 | snp | A/G | 8.25212e-05 | 0.00642291 | missense | CDC20B | GRCh38.p7 | 5:55124837 | GTTATGACTTTCAGC[A/G]GTTGGCCCTGTGCAC | 166979 |
| rs377150199 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55148681 | CCAGCCTGGGCGACA[A/G]AGTGAGACCCTGTCT | 166979 |
| rs377236718 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55157012 | AGGCTGGCTCCTTCC[A/C]TTGCACCTTATTTGT | 166979 |
| rs377409024 | snp | G/T | | | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160098 | GAAAGCAGTCAGCCT[G/T]TCCTTCCTGGTTTTC | 166979 |
| rs377427828 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55130582 | ATCTCATCAACTGGA[A/C]GATGGAAAATCTAAC | 166979 |
| rs377431544 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55154200 | CAAGGGTGGAAACCT[A/G]GGGTGCTTAGTCTAG | 166979 |
| rs377483931 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CDC20B | GRCh38.p7 | 5:55131128 | ACAGAGTGAAAACCT[A/C]CCTCAAAACCTCCCT | 166979 |
| rs377539070 | snp | C/T | | | utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55114036 | AGAGAAGAAAAGAAG[C/T]GGATCTCTGGGAAGC | 166979 |
| rs377546107 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55161733 | CTTACCAGATTTTTG[C/T]TAAAATCCAAAAACA | 166979 |
| rs377605887 | in-del | A/TTAGGTATTACATTTTCT | | | downstream-variant-500B | CDC20B | GRCh38.p7 | 5:55112516 | ATTTTCTTACAGGTA[A/TTAGGTATTACATTTTCT]TACCTGGCATATTAG | 166979 |
| rs377669720 | in-del | -/CAATATCT | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164567 | GTGACCAATGTGCCT[-/CAATATCT]TATTGTTCAACTTGA | 166979 |
| rs377708835 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55129558 | GGAAAAGTCCTAGAC[A/T]TGGGAAAGCCAAAAG | 166979 |
| rs377709857 | snp | A/G | | | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55158883 | AAAGAGAAAAAACGA[A/G]GCAATTAGATGACGT | 166979 |
| rs377729082 | snp | A/T | 0.000153988 | 0.00877328 | intron-variant | CDC20B | GRCh38.p7 | 5:55140451 | TTTCTTTAAAAACAT[A/T]CATGTACAACTAAAA | 166979 |
| rs377753011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55125726 | AGTAAGTAAATGATG[C/T]TCCACAATTATTTCA | 166979 |
| rs386688124 | in-del | AGACA/CG | | | intron-variant | CDC20B | GRCh38.p7 | 5:55135408 | GTTTAGGACAAAAGA[AGACA/CG]AGGGAGCTGAGGAAA | 166979 |
| rs397696192 | in-del | -/A | | | upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55174317 | GAAAGCAAGAAAAAA[-/A]TGGCATTAGAACTAA | 166979 |
| rs397713708 | in-del | -/G | 0 | 0 | intron-variant | CDC20B | GRCh38.p7 | 5:55153621 | GGGGTGGACTGAAGG[-/G]TTTAGTCTCTGGCCT | 166979 |
| rs397997764 | in-del | -/A | 0 | 0 | intron-variant | CDC20B | GRCh38.p7 | 5:55126487 | AAAAAAAAAAAAAAA[-/A]CAGTCTTTGGGATTT | 166979 |
| rs398093379 | in-del | -/C | | | upstream-variant-2KB | CDC20B | GRCh38.p7 | 5:55174517 | AAATTCCAGTAAATC[-/C]TTTCAGCAAACATTA | 166979 |
| rs527337972 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55142362 | AATGCTCTCCTTAAC[A/T]CCATAGAACAGCTTC | 166979 |
| rs527414349 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55141639 | ACTCTGGGTCCCCAC[A/G]GTTCAGACAGAAGTC | 166979 |
| rs527463020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55135550 | TTAGAAGGCCTGAAA[C/T]TTTGTGCCTATTTTT | 166979 |
| rs527526729 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55134766 | TAAGACATGAAGAAA[A/C]CTTAAATGCATATTA | 166979 |
| rs527569927 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55174136 | CCCTCCCTTGCTAAC[A/C]CCCCAACCATTTTTG | 166979 |
| rs527722667 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55132513 | CCTCTGCCAATCTGT[C/G]TTCTCAGTGACACCA | 166979 |
| rs527728919 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55140758 | GCCACAGCTGAATGG[C/G]CATCTTAAGGTCCTT | 166979 |
| rs527766524 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55125791 | AACTATGCAATGCTG[A/C]ACAGCATTGTGATTA | 166979 |
| rs527772310 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55171528 | CAATTAGTTTTCTCC[C/T]ACTAGAAATGACATT | 166979 |
| rs527868448 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55112975 | AACCAACGATTCAAA[C/G]AGTAATAAAAGATTT | 166979 |
| rs527899112 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55139451 | AGGAAAAGAAGAAAC[C/T]GGAGTGAGTGAGTGC | 166979 |
| rs527923808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55119466 | CTTTCAGATCGCTTT[A/G]TCTTCCACCCATTCT | 166979 |
| rs527925552 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55126277 | AGGCCGAGGCAGGTG[A/G]ATCACAAGGTCAGGA | 166979 |
| rs527949161 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55114870 | CAGATCCTTAATGAC[A/G]TCTCCAAATGCAATA | 166979 |
| rs527974762 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CDC20B | GRCh38.p7 | 5:55155953 | AAAATGCCTCCTCAC[G/T]AATGAAACCCCTTGT | 166979 |
| rs527988297 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55163755 | TTAGGTGATCCACCC[A/G]CCTCAGCCTCCCAAA | 166979 |
| rs528002079 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55145790 | TCTCTTTGTCTCTCT[C/T]CCCCCATCCATCCCC | 166979 |
| rs528033207 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55117912 | CTAAGGTCAGGAGTT[C/T]GAGCCCAGCCTGGCC | 166979 |
| rs528065757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55169895 | GAGGCGGGTGGATCA[C/T]GAGGTCAGGAGATCG | 166979 |
| rs528113253 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55155134 | AGGGATGAATGACTC[A/G]GTACTCCAAGCACAT | 166979 |
| rs528127507 | snp | A/G/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55166138 | CTGTGGCACTGCAGG[A/G/T]GTGTTTTATGCATTC | 166979 |
| rs528152717 | snp | G/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55139348 | CCCAAAAATAGTGGA[G/T]ATAATATTGATGAAA | 166979 |
| rs528184940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55162162 | GCACTTTAGGAGGCC[A/G]AGGCAGGCAGATCAC | 166979 |
| rs528198305 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, downstream-variant-500B | CDC20B | GRCh38.p7 | 5:55136069 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 166979 |
| rs528275756 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CDC20B | GRCh38.p7 | 5:55125759 | CATTTCTCAAAGTCC[A/G]GTGTCGCATTGTTTA | 166979 |
| rs528341408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55147492 | AAACATGTTATTTTA[C/T]ATGTATTTATATATA | 166979 |
| rs528514685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55151590 | ATGCTATGTCAGCTA[C/T]GTCTGCGAAAACAAC | 166979 |
| rs528533807 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55145560 | CATATTTCAGAAAGA[C/G]AGTTTGTGTTTCGGG | 166979 |
| rs528604010 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CDC20B | GRCh38.p7 | 5:55144947 | CACTGAGAAACCAGT[A/G]GATCTGATTAATCCC | 166979 |
| rs528645542 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | CDC20B | GRCh38.p7 | 5:55118143 | AATAAAAAGAAAAAG[-/A]AAAAGAAGAAGAAAA | 166979 |
| rs528853721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55162220 | GGCCAATATGGTGAA[A/G]CCCCATCTCTATTAA | 166979 |
| rs528990911 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55162878 | ACTTAGATAGGAAGG[A/C]TCATAGAGCCCAAAG | 166979 |
| rs528996012 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55155089 | TAGAAAGGAAGAGGA[A/C]GATAAGAAAAGTAAG | 166979 |
| rs529136787 | snp | A/C | | | stop-gained | CDC20B | GRCh38.p7 | 5:55128509 | TTACAAGTGAGACTT[A/C]AGTCTATGTTTTCAA | 166979 |
| rs529138445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55147567 | TTTTATATGTATTTA[C/T]GTGTAAAATGTTATT | 166979 |
| rs529174968 | snp | A/G | | | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55158684 | AAACACATCATGATC[A/G]AATGGCATAATGCCC | 166979 |
| rs529196932 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CDC20B | GRCh38.p7 | 5:55140967 | GAATTTCCTAAAAAC[A/G]TAGTGATAAATGATT | 166979 |
| rs529212849 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55154519 | GAGACCGTGTCTCCC[A/G]AGAAAAAAGAAAAAA | 166979 |
| rs529281758 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CDC20B | GRCh38.p7 | 5:55153505 | ATGTATTATTTTTCA[A/T]GGTTCTCCAATAGGA | 166979 |
| rs529321343 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CDC20B | GRCh38.p7 | 5:55169372 | TATTTCTTATATCTC[A/T]TCTATGGCTTAACTA | 166979 |
| rs529324307 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55145589 | GGGCTCTGGCAGGTT[A/G]ATCATGGATCCTGCC | 166979 |
| rs529328467 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | CDC20B | GRCh38.p7 | 5:55152034 | AGGAAGGCAGAGGGA[A/C/G]ATGTGACTGCACACA | 166979 |
| rs529347869 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55118051 | TTGAACTTGGGAGGC[A/G]GAGGTTGCAGTGAGC | 166979 |
| rs529388017 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55146028 | ATATATACATATACA[A/T]TCATACAATCTTTAC | 166979 |
| rs529476556 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55124700 | CAAATTCTAGAGAAA[G/T]AAAAATCTCAAAATA | 166979 |
| rs529493653 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CDC20B | GRCh38.p7 | 5:55132244 | ACTGTTCCCTTCAGG[A/G]ATTTTTCTTTTTCCA | 166979 |
| rs529508833 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55121343 | ATAAACAGTTTTCCA[C/T]GTTTTAATAGACTTT | 166979 |
| rs529569774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55117991 | AGGCGTGGTAGTTGG[C/T]GCCTGTAGTCCCAGC | 166979 |
| rs529619047 | snp | G/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55131450 | GTCAGGGAAATGGAA[G/T]AGAAACACAAATCAG | 166979 |
| rs529637358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55169924 | CGAGACCATCCCAGC[C/T]AACACGGTGAAACCC | 166979 |
| rs529639971 | snp | A/C/G | | | utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55113975 | AAAGGGGTAAGAATG[A/C/G]GAGGAAGAAGAGGAG | 166979 |
| rs529701346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55137106 | CGCTTGAACCCGGGA[A/G]ACAGAGGTTGCAGTG | 166979 |
| rs529778081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55168060 | GATATGAGGACACTC[C/T]ATCCATATTTAGTCC | 166979 |
| rs529805572 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55117156 | AGCTACCTACTCCTA[A/T]TTTAAAGCTTAAAAA | 166979 |
| rs529880929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55123927 | TATATATTTCAACCT[A/G]TATTAGGAAGCCCTG | 166979 |
| rs529938087 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CDC20B | GRCh38.p7 | 5:55152597 | ATCATTGTCTCTATG[A/G]ATGGCACCCTCTGGA | 166979 |
| rs529944433 | snp | C/T | 1.65542e-05 | 0.00287695 | utr-variant-5-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160176 | GCTGCTGAGACTTCC[C/T]TCTAGAATCCTCCAA | 166979 |
| rs530158240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55115259 | AGTAGTCCTATGAGA[A/G]GTTAATAGGTATTAA | 166979 |
| rs530212713 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55150040 | TTGGGAGGCTGACAA[A/G]AGAATCGCTTGAACC | 166979 |
| rs530287114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55144635 | CTTGCTCTTTGTCCT[A/G]AGAAATTATGCATGC | 166979 |
| rs530445009 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55143990 | AATGCTTTATCTCTG[C/T]ATGGAAAAAAAAAAA | 166979 |
| rs530473162 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55130679 | AATATATGAAAGAGA[A/T]ACTTGGATCTTCAGA | 166979 |
| rs530480340 | snp | A/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55132286 | TTTTTAGATATTCCA[A/T]GGAGCCCAGACCCCT | 166979 |
| rs530499276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55117250 | GGTCTCTTTAACTGA[A/G]ATTTTCCCCCCAAAA | 166979 |
| rs530541078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55162065 | TGCTTGCTCTGTGCC[A/G]GACACTGTTCTAAAC | 166979 |
| rs530560088 | snp | A/G | | | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55159427 | GGTGCATCACAGTTC[A/G]AAGGAGAAGTGTTGT | 166979 |
| rs530616058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55169788 | ACACAGTCATGGCTA[C/T]AGAAACCAATTCTAA | 166979 |
| rs530647839 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55161395 | AAGAGCCAGAATCTC[A/G]TCCTTTGTAACTTCT | 166979 |
| rs530656371 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55117733 | CTACAGATTTCCCAA[A/C]TGTGTTTGGGAAACA | 166979 |
| rs530728430 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55153585 | AGTCAGCAGATCCAC[A/G]TTAGCCTGAATAAAT | 166979 |
| rs530760634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55152773 | CTCCTTAAGACCAGG[A/G]ACTTTGTCTTTTATC | 166979 |
| rs530840418 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | GPX8, CDC20B | GRCh38.p7 | 5:55167771 | AGGAGGCTGAGGTGG[A/G]AGGATTGCTTGAGCC | 166979 |
| rs530962198 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55158740 | TTAAACAGAGCAGAA[A/T]TGAAAGTGAATGGCT | 166979 |
| rs530969357 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55125385 | TATTAACACTTTTCT[A/G]CAACTTTGAATATTT | 166979 |
| rs530978957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55151472 | GGACAGAGACACTTG[C/T]TCAAAAGTTTCCTTA | 166979 |
| rs531241638 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55149863 | TTTTGGCCAGGTGCA[A/G]TGGCTCACACCTGTA | 166979 |
| rs531254176 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55145522 | GGATGGGAATGAAAA[C/T]GTCTGTGCCCAAATG | 166979 |
| rs531274612 | snp | C/T | | | intron-variant, upstream-variant-2KB | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170798 | TTGTAACATGAAACA[C/T]AGTGGCAGAACTCTA | 166979 |
| rs531369138 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55129000 | ATATGGGAGATGCCA[C/T]CATCATTTCTAACCA | 166979 |
| rs531402488 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55139557 | CTAGTAAATGAAAAC[C/T]AAGGCAACTTTTAAT | 166979 |
| rs531513804 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55166211 | GGGCAGCAGAGACTC[C/G]CCACTGCCAGATGGA | 166979 |
| rs531626522 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55166769 | CACAGTGGCTCACAC[C/T]GGTAATCCCAGCACT | 166979 |
| rs531768389 | snp | A/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55117696 | GTGTGTTCATGGAAC[A/T]AGTACTTCAAGATGT | 166979 |
| rs531777887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55133914 | TACCTGGTACACCTA[C/T]GCCCTACTCTGAGAC | 166979 |
| rs531783747 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55142264 | ACCACATGAAGACAC[A/G]CGTTTACTCTACAGG | 166979 |
| rs531822793 | snp | C/T | 0.0368353 | 0.130617 | upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55173322 | CCGCGGCCCCGCCCC[C/T]GCCGGCCCTCTCTGG | 166979 |
| rs531828662 | snp | C/T | 1.64784e-05 | 0.00287035 | intron-variant, missense | CDC20B | GRCh38.p7 | 5:55120454 | TTGGGGTCTGGATGC[C/T]CTTCCCAGCATTTAT | 166979 |
| rs531849250 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55113074 | CAGGTAACATCATTT[C/T]AAAACACTTCCTGGA | 166979 |
| rs531880625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55149263 | ATCTTTGTACATTGC[A/G]AGTGTACAGAATGTG | 166979 |
| rs531889497 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55113753 | CTAGCATATAGTGAG[A/G]TTTTAGTAAGTGTTT | 166979 |
| rs531927342 | snp | A/G | | | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55163012 | CAAAACGGGGATGAT[A/G]ATAATACCCACCTCA | 166979 |
| rs531959040 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CDC20B | GRCh38.p7 | 5:55136371 | CAAGACCAGCCTGGG[A/C]AACATGGTGAAACCC | 166979 |
| rs532020793 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | CDC20B | GRCh38.p7 | 5:55135744 | TTGTAAAAACACTGA[G/T]ATTTTTTTGTGATTT | 166979 |
| rs532219098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55129039 | ACCCAGCTAGAAGAG[A/G]TGGTGGTTCATGTAT | 166979 |
| rs532254840 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CDC20B | GRCh38.p7 | 5:55129684 | AAAGGCTTTAAGAAA[C/T]GAACTGAGATTTGAA | 166979 |
| rs532383840 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55122578 | CTACCTTTGAATGTG[A/G]GACTTGTGACTATCC | 166979 |
| rs532473981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55116243 | TTAGTTGTTTTAAAA[A/G]GATAAATATAGGAGA | 166979 |
| rs532492122 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55113863 | AGGCAATCAGAAATA[C/T]GAGGTTTGGAGCTGG | 166979 |
| rs532492986 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CDC20B | GRCh38.p7 | 5:55156738 | AATTAGCCGGGCATT[G/T]TGGCGCGTGCCTGTA | 166979 |
| rs532500094 | snp | A/G | 0.00054359 | 0.0164772 | intron-variant, synonymous-codon | CDC20B | GRCh38.p7 | 5:55120524 | AATGGCAAGGACCCC[A/G]GACTGCCAGGGACAC | 166979 |
| rs532511656 | snp | G/T | 0.00914312 | 0.0669923 | upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55173401 | GCTTTGCCGCGAGCC[G/T]TGGCGGGCCTGCGGC | 166979 |
| rs532522948 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55121308 | CTATTTGATTATTTT[A/C]TGTTGTTTTCACCTA | 166979 |
| rs532602189 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55114485 | CATGCTGGGAGACAG[A/C]AGTCAGGGCCGACTG | 166979 |
| rs532640838 | snp | A/C | 0.00478085 | 0.0486577 | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55165889 | ATTAACACACTTACT[A/C]AGGTGTTTTAAGTGA | 166979 |
| rs532651524 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CDC20B | GRCh38.p7 | 5:55150442 | GCCTGCAGCCCCCAG[C/G]GGGCGAGGCCGGCTC | 166979 |
| rs532653042 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55173997 | TGGCGGGAAATGACA[A/G]GGAACCAGATGGGCT | 166979 |
| rs532653168 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164995 | CAAGTAAGTCAGTCT[A/T]TATTTTTGCGTGAAA | 166979 |
| rs532770829 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CDC20B | GRCh38.p7 | 5:55157243 | ATGTATAGTCTGAGA[A/G]TAGAGTTAGTATAGA | 166979 |
| rs532795320 | snp | C/G/T | 0.00159649 | 0.0282165 | intron-variant | CDC20B | GRCh38.p7 | 5:55169909 | ACGAGGTCAGGAGAT[C/G/T]GAGACCATCCCAGCT | 166979 |
| rs532815413 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55155252 | AAAGGACCCAGAGGG[G/T]TTAAAAATAAGGTCA | 166979 |
| rs532857530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55149902 | ACTTTGGGAGACTGA[A/G]GTGAGTTAATCACCT | 166979 |
| rs532908209 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | CDC20B | GRCh38.p7 | 5:55112966 | AAACAAAACAACCAA[C/T]GATTCAAACAGTAAT | 166979 |
| rs532939144 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55131977 | CAAGAGGCTGAGGCA[C/T]GAGAATTGCTTAAAC | 166979 |
| rs532996208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55148564 | ACAAAAAATACAAGA[A/G]TGAGTTGAGCGTGGT | 166979 |
| rs533062544 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CDC20B | GRCh38.p7 | 5:55126645 | AAAAGAAGCAGTTAA[A/G]CTAAATCACTAGTTC | 166979 |
| rs533139323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55142200 | TCTGAAAGTCTCCAC[A/G]GCTATGCAGGCCCTC | 166979 |
| rs533227991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55134633 | CAGGCATGCTGGTAC[A/G]TGCCTGTAGTCCCAG | 166979 |
| rs533306740 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | CDC20B | GRCh38.p7 | 5:55174934 | AGAAAGTATTAGTCA[A/G]ATATCTTTAGGAAGT | 166979 |
| rs533310299 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55116890 | GGCATTTGGACTGGA[C/T]GCAAAGACATTCTTG | 166979 |
| rs533312962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170757 | ACTGCCGATTCTCGT[A/G]GCCCAGGCAGTCACT | 166979 |
| rs533341700 | snp | A/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55121451 | CTGGACCTGTTTTGG[A/T]TTTTTGTTGTATTGT | 166979 |
| rs533407849 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | CDC20B | GRCh38.p7 | 5:55138593 | GAAGCCAAAGTAAAT[-/G]GGGGGGTTGGAGGGA | 166979 |
| rs533427892 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55125252 | AAGTCTAGATTTAAA[A/G]ATATCCTTTGATAGA | 166979 |
| rs533447111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55171455 | GACACAAAACTGCAG[C/T]AGTGTTTGGGGGAAA | 166979 |
| rs533767019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, downstream-variant-500B | CDC20B, MIR449A, MIR449B, MIR449C | GRCh38.p7 | 5:55172057 | CAGATGAAGGCTCTT[C/T]ATGAAACACGTTTAT | 166979 |
| rs533817772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55141102 | GGTCTGGAGGGAGTG[A/G]GTGGATGAGCAGAAA | 166979 |
| rs533828123 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55165230 | AAGTGTAGATCAGCA[A/G]TCACTGAACCTCTTA | 166979 |
| rs533864630 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55126085 | TAAATTTTAACAATG[A/C]AGATTAGAAAAGGAG | 166979 |
| rs533898456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CDC20B, MIR449A | GRCh38.p7 | 5:55170038 | AGAATGGCGTGAACC[C/T]GGGAGGCGGAGCTTG | 166979 |
| rs533908575 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55118188 | AACCCCAAATTTCCA[A/C]ACTTACTGACCACAT | 166979 |
| rs533957121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55120065 | ATTACAACCATTCTA[A/G]GAAAGTTTATCCCAA | 166979 |
| rs533959693 | snp | A/C | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55167295 | ATATGAATTTGGCTG[A/C]AATGTGCCCTGAAAG | 166979 |
| rs534005128 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55144321 | ACTCTCTTCTCAAGA[C/T]TGAGAAAGCCCTTTA | 166979 |
| rs534015391 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55162350 | CAGTGAGCTGAAATC[A/G]CGCTACTGCACTCCA | 166979 |
| rs534042850 | snp | C/T | | | intron-variant, upstream-variant-2KB | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170919 | CAAAAACATAAAAGT[C/T]AAACAAAAACTTTAA | 166979 |
| rs534045412 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55116381 | ACTCCAGCCTGGGCA[A/G]CATAGAAAGATCCAG | 166979 |
| rs534067453 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55156266 | ACCCTTCATATGTGG[G/T]GATTATTACAATTCA | 166979 |
| rs534095347 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CDC20B | GRCh38.p7 | 5:55154449 | TTGATCCTGGGAGGT[C/T]GACGCTGCAGTGAGC | 166979 |
| rs534228913 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55155448 | AAGACAGCCCAGGTA[G/T]CTCTGAAGCATACCC | 166979 |
| rs534231721 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | CDC20B | GRCh38.p7 | 5:55147136 | AAACATAAATATGTT[G/T]TTTTATATATTTATA | 166979 |
| rs534283020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55118952 | TCCTCTCACAAAAGT[A/G]TAGGCTCCCTGAGGG | 166979 |
| rs534351163 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170955 | TCAGAATACTTACAT[G/T]TAGGTTTTCCAAATT | 166979 |
| rs534416363 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55145825 | CCCTCTCTCTTGCTT[A/C]CTTCCTCTTACTTTC | 166979 |
| rs534539100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55138502 | GTACTCTTTAACCTA[C/T]GAAAGGAGAACTAAG | 166979 |
| rs534562164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55131960 | CTACACGCCCAGCTA[C/T]TCAAGAGGCTGAGGC | 166979 |
| rs534623491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55139505 | CGGAATAAAACATTG[A/G]AGCATTTAGAGGAAA | 166979 |
| rs534649627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55132663 | CATTCTGCATACTCT[A/G]CCATGAATTTTCCTT | 166979 |
| rs534660355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55117353 | AACTTTGTGACCACA[A/G]TCCACAGCCAAAACT | 166979 |
| rs534738111 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55144080 | TAGTGGAAAGAGTAT[C/T]TGGTTTGCCCGAGCT | 166979 |
| rs534854090 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | CDC20B | GRCh38.p7 | 5:55128848 | TTATTTACACTGAAA[-/T]TATATTTATTTAGAG | 166979 |
| rs534991450 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55116437 | TATAATAGAACATTA[C/T]TCTAATGCTTTTATT | 166979 |
| rs535039085 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CDC20B | GRCh38.p7 | 5:55124237 | GACCCAGGCCCATCA[A/G]TGTGCCCATCTCTCT | 166979 |
| rs535112923 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55129384 | GAGAAGCAAACTGGC[C/G]GGGGGTAAGTTTCCC | 166979 |
| rs535176494 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55153443 | TTGTTAGTGATCTAT[A/G]AGCAAAACATGACAA | 166979 |
| rs535228905 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55123140 | TCTTGGTCTCATATG[G/T]TGAATTAATGTACGG | 166979 |
| rs535238836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55130097 | TTTATATGAAACTTT[A/G]TATGAAGCTTTAACA | 166979 |
| rs535260522 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55157911 | ACACGGCTCAAATTA[C/T]AGCAGGTATTCTATG | 166979 |
| rs535325984 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55122397 | CTACCTCAGCCTCCC[A/G]AAGTGCTGGGATTAC | 166979 |
| rs535365428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55171083 | CTTTGGGAGGCCAAG[A/G]TTGGCTGATCCCCTA | 166979 |
| rs535413535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55153693 | ATTTATCAAAATTGT[C/T]GATTACTCTAAGCTG | 166979 |
| rs535516412 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55137452 | CAGCATTTGGATAAC[A/G]TTTGTCCCCGTGATC | 166979 |
| rs535554105 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55146221 | GCTGAGCTTCAGTCA[A/G]TCACAGGCGGCCAAC | 166979 |
| rs535674658 | snp | C/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55119388 | TGGTCTACCTTGAAA[C/G]GGCAGATGTTCACAG | 166979 |
| rs535790134 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55123627 | GCTCTGGTTTCCGGA[C/G]ACTCTCTCTTAGTGA | 166979 |
| rs535808006 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55156747 | GGCATTTTGGCGCGT[A/G]CCTGTAGTCCCAGCT | 166979 |
| rs535828129 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55146039 | TACATTCATACAATC[G/T]TTACAAAAGTAATCA | 166979 |
| rs535877462 | in-del | -/A | 0.0023933 | 0.0345097 | downstream-variant-500B | CDC20B | GRCh38.p7 | 5:55112835 | AATTCATGTCAAAGC[-/A]AAAAAAAATAATCAA | 166979 |
| rs535911650 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CDC20B | GRCh38.p7 | 5:55131027 | CTTGGGAGGCTAAGG[C/T]AGGAGGATCACTTGA | 166979 |
| rs535928594 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55158862 | CAACAGCCAGGGGAG[A/G]GAAATAAAGAGAAAA | 166979 |
| rs535947884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55115735 | AATTTCAGAAATGAT[C/T]GTGTACTCTGATACA | 166979 |
| rs536013045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55150936 | TTTTTTGGAGAGACG[A/G]GGTTTCACCATGTTG | 166979 |
| rs536048549 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CDC20B | GRCh38.p7 | 5:55116572 | TTCCACCTCAGTCTC[C/T]CAAATAGCTGGGACT | 166979 |
| rs536130546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55161696 | TTATCTGAAACAATA[C/T]TCTCAAAGATGAATA | 166979 |
| rs536141501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55153060 | CCTCGACAATGTGGC[A/G]AAACCCCATCTGAAC | 166979 |
| rs536153524 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CDC20B | GRCh38.p7 | 5:55145116 | GGAGCCCCTAATTTT[A/C]GCCAGAAATTCTTCC | 166979 |
| rs536265458 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | CDC20B | GRCh38.p7 | 5:55174784 | AATTTCTTACAAGTA[C/T]TAAGAATAGTGAATC | 166979 |
| rs536279973 | snp | G/T | | | synonymous-codon, intron-variant, missense, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164119 | CCCTGAGGGTCAAGT[G/T]GTGAAGTTCTGGAAG | 166979 |
| rs536347185 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55165476 | TGTGACTTGACTCCC[A/G]AATTCTGACCTGATG | 166979 |
| rs536576982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55127589 | GATATATGGCAGTTG[C/T]TTTAAAGCTCCCCAG | 166979 |
| rs536623437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55156823 | AGGTTGCAGTGAGCC[A/G]AGGTTGCACCACTGC | 166979 |
| rs536680974 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55126226 | TTTGGGATGGCCAGG[C/T]GCGGTGGCTCACACC | 166979 |
| rs536749516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55142702 | ATATCCAACAATAAA[A/G]CACACATCAAAATAC | 166979 |
| rs536762117 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55149375 | CCACTCATAGGTATA[A/C/T]GTACTCAAACTCAAA | 166979 |
| rs536792673 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CDC20B | GRCh38.p7 | 5:55150127 | ACAAGAGTGAAACCC[C/T]GTCTCAAAAAAATAA | 166979 |
| rs536873212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55145246 | CCTACTGCTTCCCTC[C/T]TCGGTTATTAAATAC | 166979 |
| rs536884420 | snp | A/G | | | intron-variant, utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55137134 | GTGAACTGAGATCGC[A/G]CCACTGCACTCCAGC | 166979 |
| rs536961817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55145751 | CCTCCTCCTCCTCCT[C/T]TGTCTCCTCCTCTCT | 166979 |
| rs536963883 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55137488 | ATGAGCAATTACTTG[G/T]CTTATGTGGGATCTG | 166979 |
| rs537018993 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55158911 | CGTGCCCAAGTAGAG[A/G]TGGGTTTTGCAGGGT | 166979 |
| rs537064486 | in-del | -/TA | | | intron-variant | CDC20B | GRCh38.p7 | 5:55150152 | AAATAAATAAAAAAT[-/TA]AAAAATAAAGGTTTT | 166979 |
| rs537084281 | snp | A/T | | | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55159373 | ATGAAATCATTTTGA[A/T]AGGTCAGAACTGGGT | 166979 |
| rs537221654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55129283 | CCATGATAAATATAA[A/G]CTCTGAATGAAATAT | 166979 |
| rs537335647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55122865 | TTAGCTTCCGATGCT[A/G]TCTGACTGCAACCTC | 166979 |
| rs537337658 | snp | G/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55157648 | TTCTGGTGTAAAAAC[G/T]GGCTTATTCAGCAAT | 166979 |
| rs537504342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CDC20B | GRCh38.p7 | 5:55136035 | TGCAACTTCCGCCTC[C/T]CTGGTTCAAGCAATT | 166979 |
| rs537524476 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164346 | GCAGTAGTGCGTTCT[C/G]AGCTCATTGCAACCT | 166979 |
| rs537555928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55143674 | TTATCTTTGAATTTG[A/G]TTTTTAAAACAAGAT | 166979 |
| rs537592863 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB | CDC20B | GRCh38.p7 | 5:55174846 | ACATTTATAAATTCC[A/G]TTATAGCCATTAATT | 166979 |
| rs537677265 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55149898 | CAACACTTTGGGAGA[A/C]TGAGGTGAGTTAATC | 166979 |
| rs537812821 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55119516 | AAAATAAGATGATTT[A/G]TGATGCTAACTCGAG | 166979 |
| rs537867290 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CDC20B | GRCh38.p7 | 5:55115917 | ACACCACACACACAC[A/G]CACCAGTAAAGGATG | 166979 |
| rs537884553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55134259 | CCAGGTGACTTGTGG[C/T]GTCTATGACCAGATG | 166979 |
| rs537899463 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55141023 | TCTTCACAATAAAAT[A/G]TTTGCTCTCCCAAAT | 166979 |
| rs537929053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55120179 | AGCCAGATTACTCTC[A/G]AAGTTCATGGTCAAA | 166979 |
| rs538013239 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55165504 | ATGGATGAAAGTGAA[G/T]ATGTTTCGTATGGCA | 166979 |
| rs538071521 | snp | G/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55116624 | GGCTAATTTTTGTAA[G/T]TTTTCTAGAAATGGA | 166979 |
| rs538106899 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CDC20B | GRCh38.p7 | 5:55133676 | TACAGTACAAAGAGC[C/T]GGGGAAGGAAGGAAA | 166979 |
| rs538125062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55149456 | GACAACCCAAACACT[C/T]ATCAACAGATGAATG | 166979 |
| rs538144580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55156853 | CACTCCAGTCTAGCC[A/G]ACAGAGTGAGATTCT | 166979 |
| rs538227599 | snp | C/G | 1.64844e-05 | 0.00287087 | missense | CDC20B | GRCh38.p7 | 5:55128558 | CATTCCAGATGTATA[C/G]AGCAGAGCCCAGGGC | 166979 |
| rs538330988 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55166275 | TGTCCCAGTCAACAT[A/G]ATACAGATGAACATC | 166979 |
| rs538340109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55163071 | ATCAATTTGAAGCAC[A/G]GAGCGTACATTAATC | 166979 |
| rs538403396 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC20B | GRCh38.p7 | 5:55174530 | ATCTTTCAGCAAACA[C/T]TAAGACTAAATAAAA | 166979 |
| rs538466289 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | CDC20B | GRCh38.p7 | 5:55146424 | AAAGTTTTGTTTTTG[-/T]TTTTGTTTTTAAACA | 166979 |
| rs538548541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55150821 | ACAATCATGGCTCAC[C/T]GCAGTCTCGACCTCC | 166979 |
| rs538600596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55121175 | GGACATTTTAACAAA[C/T]ACTACAGTTATATGT | 166979 |
| rs538621638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55155655 | GTAGGCAATATGACC[C/T]ACACACTGTCAAGGT | 166979 |
| rs538637357 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55127540 | AGTCTATAACACTAT[C/G]GATGCTGATTTAGTT | 166979 |
| rs538694671 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55119999 | GGTTACAGGCAGTAT[G/T]CACTGTCCATGACCC | 166979 |
| rs538696459 | snp | C/T | 0.00159617 | 0.0282053 | downstream-variant-500B | CDC20B | GRCh38.p7 | 5:55112648 | CATTACCAAACAGAT[C/T]TAAATTTAAAAAACA | 166979 |
| rs538753723 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55133229 | GCCAACATTAACAAT[A/C]CCATCCCTAAATATG | 166979 |
| rs538900655 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55135155 | GACAAGGGATATAAG[A/G]GAACCTGCACCTTCT | 166979 |
| rs538932329 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CDC20B | GRCh38.p7 | 5:55150175 | AAAGGTTTTTTTAAA[C/T]ATGTGCATTTCACTT | 166979 |
| rs538962449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55142542 | AAGGAAAAGGAAGTC[C/T]TAAGGGGTAGGGCAG | 166979 |
| rs538964489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55134294 | CTGATAAAAGCATGA[A/G]AGCTTCACAATGCTA | 166979 |
| rs539098736 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55125820 | TAACAATATGGGCTC[C/T]GGAGCCAGACCAGCT | 166979 |
| rs539265851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55125535 | GCTAAAGAACTAAAC[C/T]TCTTTGTAAAAGAAG | 166979 |
| rs539269812 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55149328 | GATACCTCAAAAAGA[G/T]AAACCTAGAATTACC | 166979 |
| rs539356806 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55132927 | TAAATATCTCCACAA[C/T]GTCTTTCTGGACAAC | 166979 |
| rs539469101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55139698 | TTTTAAAGTGTGATA[C/T]AAGCATGTCGAGAAA | 166979 |
| rs539469543 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CDC20B | GRCh38.p7 | 5:55147013 | CTAGATATTATTTTA[C/T]ATATTTGTATATATT | 166979 |
| rs539557073 | snp | A/G | 0.000231566 | 0.0107578 | intron-variant | CDC20B | GRCh38.p7 | 5:55140429 | ATAAACACACATAAG[A/G]AGAATATTTCTTTAA | 166979 |
| rs539585213 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55169374 | TTTCTTATATCTCAT[C/G]TATGGCTTAACTAAC | 166979 |
| rs539592363 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55126909 | GCTTAACATATTCCA[C/T]AGTATAGATACTGAC | 166979 |
| rs539609837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55161774 | TTTTTTCAGAGGGCA[A/G]TAGTGTTAGGCTATT | 166979 |
| rs539721842 | snp | C/T | 1.64751e-05 | 0.00287007 | intron-variant, upstream-variant-2KB | CDC20B, MIR449B, MIR449C | GRCh38.p7 | 5:55172653 | GCATGATACTTTCCT[C/T]TGAAAACACAGATAA | 166979 |
| rs539750193 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55153830 | TTATTTAGATTTTTT[C/T]TCTTCATTGCACAGG | 166979 |
| rs539797846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55131783 | GAAAGAGGGCTGTGC[A/G]TCTGGGCATGGTGGC | 166979 |
| rs539863480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55125094 | TGAAAACATGGAGGA[A/G]AGCATAGTTCAAAGT | 166979 |
| rs539908361 | snp | C/G | 1.85221e-05 | 0.00304314 | intron-variant | CDC20B | GRCh38.p7 | 5:55124773 | GGCCTCTGAGTAACA[C/G]GAAACCTAGAAATCT | 166979 |
| rs539925113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55117590 | GTGTATGTCAAGAGC[A/G]CTGTTCTTGACCCAC | 166979 |
| rs540020439 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | CDC20B | GRCh38.p7 | 5:55112768 | TCTTAAAGTTTTTGT[C/T]TTGTTGTGTTGATTT | 166979 |
| rs540126428 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55162263 | TAGCCAGGTGTGGTG[A/G]TGGGCACCTGTAATC | 166979 |
| rs540155630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55137418 | TATGGACAAGGCATA[A/G]AGAATTGCTTTATAT | 166979 |
| rs540195460 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55170030 | GAGGCAGGAGAATGG[C/T]GTGAACCCGGGAGGC | 166979 |
| rs540252416 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160018 | ATTCTGTAGAGCTCC[G/T]TGCTTCATTCAGGAG | 166979 |
| rs540264433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55132812 | AAATATCTTAATTAC[C/T]AACATCCTGCCTTCT | 166979 |
| rs540312223 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55153903 | AGTGTTAGGCAGACC[A/C]CACTACAATATGAGC | 166979 |
| rs540335728 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55139504 | ACGGAATAAAACATT[A/G]GAGCATTTAGAGGAA | 166979 |
| rs540335956 | snp | C/T | | | intron-variant, upstream-variant-2KB, downstream-variant-500B | CDC20B, MIR449A, MIR449B, MIR449C | GRCh38.p7 | 5:55172218 | TATGCCACTTCTCCA[C/T]ATTGTCCACAAGATG | 166979 |
| rs540357018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55171300 | CCTGGGCAACAAAGT[A/G]AGACTCTGTCTCAAA | 166979 |
| rs540359336 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55125598 | AATATGATTCCTAAG[C/G]AGTGGATAATGTCTC | 166979 |
| rs540419955 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55153334 | TGAGATAAATGAAAC[A/C]ACAAAAGTGTATCTG | 166979 |
| rs540454046 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55162868 | GTGTCATTCCACTTA[C/G]ATAGGAAGGATCATA | 166979 |
| rs540482351 | in-del | -/GTCAGGA | | | intron-variant | CDC20B | GRCh38.p7 | 5:55126276 | AGGCCGAGGCAGGTG[-/GTCAGGA]GATCACAAGGTCAGG | 166979 |
| rs540508201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55148439 | AAGAAATCAGCCGGC[C/T]GTGGCGGCTCATGCT | 166979 |
| rs540583954 | in-del | -/ACA | 0.0023933 | 0.0345097 | intron-variant | CDC20B | GRCh38.p7 | 5:55146950 | AATGACTCATCTAGT[-/ACA]ACACCAATAAAATAT | 166979 |
| rs540593440 | snp | C/T | | | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55158374 | AACACATCTTACATA[C/T]ATTTTTGTTCTTTAC | 166979 |
| rs540627612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55117627 | AACACAGCCTCACAA[C/T]GAAAGCCATAAAAAT | 166979 |
| rs540680236 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CDC20B | GRCh38.p7 | 5:55129721 | ATACAAGTCTCAGCC[C/T]AGGCTCTGATCCACA | 166979 |
| rs540721867 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55137563 | GCATAGAGTATTCAG[A/C]GGGCCTCTCAATTAG | 166979 |
| rs540735873 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55137013 | GCCAACATGGTGAAA[A/C]CCCTTCTCTACTAAA | 166979 |
| rs540924672 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55132232 | GGGAGATAGAGAACT[C/G]TTCCCTTCAGGGATT | 166979 |
| rs540956392 | snp | G/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55131775 | GGAGGAAAGAAAGAG[G/T]GCTGTGCGTCTGGGC | 166979 |
| rs540997346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55123894 | ATTGGGCCAGTACAA[C/T]GTAGTGGCAGCAGTC | 166979 |
| rs541198100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55128771 | AATCCTTAAAAGTTC[A/G]AAAATGAAAAGTGGA | 166979 |
| rs541233865 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55115087 | TCCCACTGGGCCCCA[C/G]GTTTCAATAAACTAA | 166979 |
| rs541290641 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55124662 | AGGGTTGTCTTTCAG[G/T]AGAGTGATGACAAAC | 166979 |
| rs541312379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55124333 | TTTCCACCAGAGTTA[C/T]AAGGAAAAATGGCTT | 166979 |
| rs541411033 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55174021 | ATGGGCTGTGCAGCC[C/T]TAGCTGCCCATCTGA | 166979 |
| rs541433649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55128325 | TTCAAGAGCCACACC[C/T]AGTTTCTCTATTTTA | 166979 |
| rs541469303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CDC20B | GRCh38.p7 | 5:55136100 | AGGCACCCGCCACCA[C/T]GCCTGGCTAATTTTT | 166979 |
| rs541487190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon | CDC20B | GRCh38.p7 | 5:55137635 | GCTGCCACTAAAGTG[A/G]TCTATGGGAAGGGGA | 166979 |
| rs541523126 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55123945 | TTAGGAAGCCCTGTA[A/C]TAACTTTTAAATCCT | 166979 |
| rs541526410 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55155301 | CAACTGAGAAAATAG[A/C]AACAAATATGTCTAC | 166979 |
| rs541537780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55130605 | AATCTAACAGAAGTC[C/T]GTGCCAACTGACCTG | 166979 |
| rs541572955 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55116961 | ATAGTGGGAAATGTC[A/G]TCTTTATCTCGGACA | 166979 |
| rs541635410 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55124504 | CAAAGCCTTAGATCC[A/T]GCTGATATTTAAAAC | 166979 |
| rs541670107 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55166517 | CGGGGTTCTGTAACA[A/G]TTAGGCTATGTGTGC | 166979 |
| rs541709905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55118334 | GAGCTCAAAAGTAAC[C/T]TCATCTCCAACTATA | 166979 |
| rs541724721 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55126530 | TCTACCTTAACCTTA[A/C]GAACTACAATATGAA | 166979 |
| rs541755309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55150447 | CAGCCCCCAGGGGGC[A/G]AGGCCGGCTCTCTCT | 166979 |
| rs541790731 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55159011 | GAGTTCAATTTTTGC[G/T]TTTTTCCCTCTTCTT | 166979 |
| rs541801512 | snp | C/T | 1.70787e-05 | 0.00292217 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55161274 | AATATCTGCCTTGCA[C/T]ATGCTGTTTTAAATT | 166979 |
| rs541919287 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55138922 | GAGTCAATCCAGGAT[A/T]TTTCATAAAGAAGGA | 166979 |
| rs541999791 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | GPX8, CDC20B | GRCh38.p7 | 5:55167707 | CTCCACAAAAAAAAT[C/G]AAAAAATTAGCTGGG | 166979 |
| rs542055337 | in-del | -/A | 0.00597247 | 0.0543191 | intron-variant | CDC20B | GRCh38.p7 | 5:55138009 | CCCACACATACACAC[-/A]ACACCCTGCCCAACC | 166979 |
| rs542086825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55161989 | GGCTATCAATAGTAC[C/T]GCCTTCTTAAGATTG | 166979 |
| rs542147672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55145483 | TACATCAGCTGATGA[C/T]AGGTGGCAAATTTTG | 166979 |
| rs542148910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55133809 | GATCTTGTGAGGAGT[A/G]CACAGAGATACTACA | 166979 |
| rs542150155 | snp | C/T | 0 | 0 | intron-variant, downstream-variant-500B | CDC20B, MIR449A | GRCh38.p7 | 5:55170108 | GACAAAGCGAGACTC[C/T]GTCTCAAAAAAAAAA | 166979 |
| rs542162230 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55166740 | AACAGAAAAATATCA[A/G]CATCAGAGCCTGGCA | 166979 |
| rs542175622 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55157169 | TCATTTACTGAAAGA[C/G]CGCTGGTGGTTTTTC | 166979 |
| rs542226704 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | CDC20B | GRCh38.p7 | 5:55175130 | ACTTTTCACTGGCCA[A/G]AACTGGCAGAGACCA | 166979 |
| rs542258355 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CDC20B | GRCh38.p7 | 5:55129491 | CCACCATATTTCTGG[G/T]CAGAGAAACCATGGA | 166979 |
| rs542280126 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55165597 | AAACCAAAAATATTT[C/T]ATGAAGCATCTTCTG | 166979 |
| rs542299672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55150317 | AATACAGTCCTACTT[C/T]CTAGCTCTAAATGAA | 166979 |
| rs542319788 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55159294 | AGTGCTGGGATTACA[C/G]GCGTGAGCCACCATG | 166979 |
| rs542337151 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55115287 | TAAAAACAAAAAGAC[C/T]GTTTAATGTTCACAC | 166979 |
| rs542407743 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55159690 | TCTTTCCACTATAAA[C/T]TTCCTGAACTCATAT | 166979 |
| rs542431799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55143776 | TCACTCCAAAGTCCA[C/T]TGCAGAGAGCAGGAC | 166979 |
| rs542510649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55144648 | CTGAGAAATTATGCA[C/T]GCTTGCTTTCTTGTG | 166979 |
| rs542542187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55152241 | GGACCTCTGGCCTCC[A/G]TAACTAGAAGAGAAT | 166979 |
| rs542568981 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | CDC20B | GRCh38.p7 | 5:55136197 | GTGATCCACCTGCCT[C/T]GGCCTCCCAAAGTGC | 166979 |
| rs542664064 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55126353 | AAAATACAAAAATTA[A/C]CCAGGCATGGTGGTG | 166979 |
| rs542709175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55134407 | ATTACTAAAAATACT[C/T]AGGCTTGCTGATAAA | 166979 |
| rs542765282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55142080 | CTGATCACAGCAAGG[C/T]TTAGCAGGCGCTTCT | 166979 |
| rs542782943 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55138874 | ATAAAAAAGTGAGAT[A/G]AAAAATAGAAGATAA | 166979 |
| rs542789837 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55129487 | AAGGCCACCATATTT[C/T]TGGTCAGAGAAACCA | 166979 |
| rs542981574 | snp | A/C | | | missense, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55161146 | GGAGCCCCGCCCAAG[A/C]AAGGAAGTAGAATCT | 166979 |
| rs542984031 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55173887 | AGTGACAGGCAGGAC[C/T]TCATAAGGCGTGAAG | 166979 |
| rs543019783 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55130990 | ACCTGGGCATGGTGA[C/T]ATGTGCCTGTGGGCC | 166979 |
| rs543041580 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | CDC20B | GRCh38.p7 | 5:55146988 | ATGAGATTTTTTTAA[-/T]TTTTGTAACCTAGAT | 166979 |
| rs543118279 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55131239 | ATTGCAAGATGTTTA[C/T]ATATTGTGTGATGTG | 166979 |
| rs543160809 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55173171 | CCACTCCTCCCACCG[C/T]CGCTGCAAGGTGTTC | 166979 |
| rs543339583 | snp | C/T | | | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55158542 | AGCCACCCGAAAACA[C/T]ACATGCCACAGAGCG | 166979 |
| rs543495799 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | CDC20B | GRCh38.p7 | 5:55136307 | GTTCACACCTGTAAT[A/C]CCAGCACTTTGGGAG | 166979 |
| rs543585174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55114382 | TGCTGCTCAGGACTG[C/T]AGGCAATGTAAGTTG | 166979 |
| rs543617830 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | CDC20B | GRCh38.p7 | 5:55121287 | GTAGCAAACATCGTG[C/T]TTATACTATTTGATT | 166979 |
| rs543624210 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55151646 | CCTACCGCCTTAGCA[A/G]GTCTGAGTTTCTGTG | 166979 |
| rs543624655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55129006 | GAGATGCCACCATCA[C/T]TTCTAACCAAAAACA | 166979 |
| rs543689120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55149893 | AATCCCAACACTTTG[A/G]GAGACTGAGGTGAGT | 166979 |
| rs543693267 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55114933 | GATTTAGCATGGGTA[A/T]CCTTTAGGAGACCAT | 166979 |
| rs543714875 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55120973 | CCAGGTAGTGGTCAG[A/G]TAAGAGAAAAGAGAA | 166979 |
| rs543736660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55123230 | CATAAGTTAAAGTTC[C/T]CTGCTTTAATTGTCT | 166979 |
| rs543817883 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55171311 | AAGTGAGACTCTGTC[C/T]CAAAAAAATAAATAA | 166979 |
| rs543826720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55134544 | AGGCAGGCAGATTGC[C/T]TGAGCCCAGGAGTTT | 166979 |
| rs543850957 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55125322 | AAAATAAGCTGAGAA[A/G]ATTACCAGATTTTCC | 166979 |
| rs543885213 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55148826 | ACGTTTGTATTTAAT[C/T]CTAAGAAACATCTGT | 166979 |
| rs543922142 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55157550 | GACAGGAGATATACA[A/C]GTAAGTTTTCAAAGT | 166979 |
| rs543961083 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55173327 | GCCCCGCCCCTGCCG[A/G]CCCTCTCTGGGCCCC | 166979 |
| rs543962988 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164340 | TGGAGTGCAGTAGTG[C/T]GTTCTCAGCTCATTG | 166979 |
| rs543978479 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55145315 | TGATTTGAAAAAAAT[C/G]TGGGCTCCCTTTCAA | 166979 |
| rs544136975 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55157202 | ACATACTACCCCTTA[C/T]GCAGAGAAATGTGCC | 166979 |
| rs544166786 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55142525 | CCAGAAAGGATAAGA[A/G]GAAGGAAAAGGAAGT | 166979 |
| rs544200792 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55119708 | TGTACTTAGAAAAAC[A/C]AGAAGGATAAAATCT | 166979 |
| rs544275941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55155831 | GCTGCTCTGCAGACC[C/T]CCCGTGGCCCCTTCC | 166979 |
| rs544280055 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | CDC20B | GRCh38.p7 | 5:55112907 | CACCAAAAAATATAA[C/T]GCATGCTCCCTCAAG | 166979 |
| rs544290945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55147420 | AATATGTTATATTTT[A/G]TATATTTTTATATTG | 166979 |
| rs544299465 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55146571 | ACAAAGATTCTCTCA[A/G]GAATATATCTTTTAT | 166979 |
| rs544319187 | snp | C/T | | | utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55113622 | AAGCACAGAGCAGAA[C/T]AATCAGGAGGTTCCC | 166979 |
| rs544507816 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55142153 | TTACTACTTTAATCA[G/T]CAACTTAATATGGAG | 166979 |
| rs544565405 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164414 | GGATTTTTTTTTAAT[A/G]TTATCTTGCTATTAA | 166979 |
| rs544628719 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55163708 | AGATGGGGTTTCACC[A/G]TGTTGGGCAGGCTGG | 166979 |
| rs544635645 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55155912 | TTCCCCTTTCTGGGC[A/G]CTTATACAGTGATTT | 166979 |
| rs544684750 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CDC20B | GRCh38.p7 | 5:55120332 | GACTCAATAGAGAAA[A/G]AGAGCTTGTTGGGGG | 166979 |
| rs544761491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55156941 | ATTTACTGCCTTGTA[A/G]TCCTTCCGTTTCTTG | 166979 |
| rs544815467 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55140604 | TGCTGAGCATTTTAC[A/G]TATATTATTTCTCAA | 166979 |
| rs544893958 | snp | A/G | | | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55162683 | TCCTCTTATTTTGAA[A/G]GTCCACTGAGGAAAG | 166979 |
| rs544898033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55137967 | CAGAGAAGACTGAGA[A/G]GTGGGTTAGTTAAAA | 166979 |
| rs544910335 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55135116 | GGGAGATGTTGATAA[C/T]GGGGGAGGCTGTGCA | 166979 |
| rs545072251 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55149204 | TGGCTAGAATTTTTT[A/T]AATGGAAACTAATAA | 166979 |
| rs545103727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55140717 | TTTAGCCTATACACC[A/G]TAGGCCAGTGATATC | 166979 |
| rs545133855 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55156635 | AATCCCAGCACTTTG[G/T]GAGGCCGAGGCGGGC | 166979 |
| rs545176119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55148357 | TTTTGGACAATGTGC[A/G]TCAAAAGCCTTCATA | 166979 |
| rs545292460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55125777 | GTCGCATTGTTTAAA[A/G]CTATGCAATGCTGAA | 166979 |
| rs545330983 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, nc-transcript-variant | CDC20B, MIR449A, MIR449B, MIR449C | GRCh38.p7 | 5:55172316 | TTAAAATCATTAACA[C/G]CCGCTAGCAATACAC | 166979 |
| rs545353090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55147483 | ATATTTATAAAACAT[A/G]TTATTTTATATGTAT | 166979 |
| rs545373248 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55127045 | GTGCATCCCATGCAG[A/T]AGGCACACATGATAC | 166979 |
| rs545435302 | in-del | -/G | 0.00478085 | 0.0486577 | intron-variant, utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55137112 | AACCCGGGAGACAGA[-/G]GTTGCAGTGAACTGA | 166979 |
| rs545490497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55117829 | CCTTAAGAAAGAAAA[C/T]AGTGGCCAGGCATGG | 166979 |
| rs545513160 | snp | G/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55127130 | GGATCATACCTGATA[G/T]TAAGTCCAATGGCCT | 166979 |
| rs545523806 | snp | C/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55125273 | CTTTGATAGATGTTT[C/G]TAATGACTTTAATCT | 166979 |
| rs545716333 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55126260 | AATCCCAGCACTTTG[A/G]CAGGCCGAGGCAGGT | 166979 |
| rs545807398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55167806 | GAGGTCAAGGCTGCA[A/G]TGAGCCGACATGGCT | 166979 |
| rs545879575 | snp | A/C | 3.34085e-05 | 0.00408695 | intron-variant | CDC20B | GRCh38.p7 | 5:55125032 | AGTCTTGACCCACTG[A/C]GAGTTTACATAACAA | 166979 |
| rs545945976 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55137937 | CTTGCAAAATCCCAC[A/G]AGGGCTCCGAGGCAC | 166979 |
| rs545956317 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55169861 | GCTCACGCCTGTAAT[C/G]CCAGCACTTTGGGAG | 166979 |
| rs545959911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55152308 | TGCAGCAGCCCTAGG[A/G]AACAAATACTCAGCC | 166979 |
| rs546021199 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55159857 | ATACACAGCTTAGCA[C/T]GGGGAATGAGCCCTC | 166979 |
| rs546063117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55154765 | GAACACTAATAATTA[C/T]GTATTTAATGTCATT | 166979 |
| rs546076161 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CDC20B | GRCh38.p7 | 5:55146018 | GTACATATACATATA[C/T]ACATATACATTCATA | 166979 |
| rs546080082 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55117415 | CATACATGTACTACA[C/T]AACTATAACATAAGT | 166979 |
| rs546083137 | snp | G/T | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55159439 | TTCAAAGGAGAAGTG[G/T]TGTTTCTCAGTTGTG | 166979 |
| rs546118795 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55150128 | CAAGAGTGAAACCCC[A/G]TCTCAAAAAAATAAA | 166979 |
| rs546132615 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55159359 | TGCATCGGTGAATGA[C/T]GAAATCATTTTGATA | 166979 |
| rs546166068 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55162825 | CCCTTCTTAGCCTGT[G/T]TAATCAAAAAGGTAA | 166979 |
| rs546194343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55116916 | TCTTGAAGTTTTTCT[C/T]TCACATCAGTGACAA | 166979 |
| rs546386478 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55145537 | TGTCTGTGCCCAAAT[A/G]AGAATTACATATTTC | 166979 |
| rs546501555 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55146193 | CTTAGCTGAGTCTCC[A/G]CCAATCACAGAAGCT | 166979 |
| rs546525694 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55137731 | TTTTCAACCTAAGTA[C/T]AGCAAATGACTTTTT | 166979 |
| rs546565087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55140802 | TTCACAGAGCTCTTA[A/G]GTAACTTTACTAAAA | 166979 |
| rs546572830 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55161639 | ATAGTGCTGGGCATT[A/G]TTAGTTAACATATGT | 166979 |
| rs546640532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55144963 | GATCTGATTAATCCC[C/T]AGTATTAACTTCAGT | 166979 |
| rs546734751 | snp | G/T | 4.94311e-05 | 0.00497123 | missense | CDC20B | GRCh38.p7 | 5:55146702 | AGGTAGGTGGTTGAC[G/T]GCTCTTCCCCAAAGG | 166979 |
| rs546751975 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55162174 | GCCGAGGCAGGCAGA[C/T]CACTTAAGGTCAGGA | 166979 |
| rs546758044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55153687 | AGATTTATTTATCAA[A/G]ATTGTTGATTACTCT | 166979 |
| rs546922203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55140244 | AATAATATATTTTAA[A/G]ATTAGGAAGAAATGA | 166979 |
| rs546934396 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55152458 | AGTTTCATCACAACC[C/G]TCTGAAATAGGTACT | 166979 |
| rs546966348 | snp | A/G/T | 0.000677534 | 0.0183936 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55128583 | CAGGGCTATGGCAAC[A/G/T]AGATTCTGAAAACTC | 166979 |
| rs547016917 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55124135 | GAGAAATAAATAATT[A/T]TGCAGAACATGGTGG | 166979 |
| rs547017951 | snp | A/G | | | intron-variant, downstream-variant-500B | CDC20B | GRCh38.p7 | 5:55136288 | GGACACGGCAGGTGC[A/G]GTGGTTCACACCTGT | 166979 |
| rs547071230 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55156780 | TCGGGAGGCTGAGGC[C/T]GGAGAATCACTCAAA | 166979 |
| rs547121407 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55145573 | GAGAGTTTGTGTTTC[A/G]GGGCTCTGGCAGGTT | 166979 |
| rs547130932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55129084 | CTCAACAGTATTCTA[C/T]AGCTTATACTAATAA | 166979 |
| rs547198310 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55167009 | CACTCCAACCTGGGC[A/G]ACAGAGCGAGACCCC | 166979 |
| rs547225141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55124583 | ACTTTTTTGCTTAAG[C/T]TTAAGTTTGACTTTG | 166979 |
| rs547241956 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55125638 | TCAGTGATGTGAATC[C/T]AAACAACTAAAGATC | 166979 |
| rs547295641 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55132667 | CTGCATACTCTGCCA[C/T]GAATTTTCCTTTGAT | 166979 |
| rs547321619 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55159410 | AAAATGCAACAGGTG[A/G]GGGTGCATCACAGTT | 166979 |
| rs547361306 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC20B | GRCh38.p7 | 5:55174625 | AACTAAAACTCAAAG[C/T]ATATTGGAAATAATA | 166979 |
| rs547492617 | snp | A/G | 1.64806e-05 | 0.00287054 | intron-variant | CDC20B | GRCh38.p7 | 5:55120576 | TCACATAATAGCACA[A/G]ACAGGTCAGCTTCAA | 166979 |
| rs547514754 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55113879 | GAGGTTTGGAGCTGG[A/G]GAGAAAAGTCATACG | 166979 |
| rs547637438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55149970 | GAAACCCCATCTCTA[C/T]TAAAAATACAAAAAT | 166979 |
| rs547669408 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55135824 | TTCTATATGTGGCCC[A/T]AAACAATCCTTCTTC | 166979 |
| rs547700623 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CDC20B | GRCh38.p7 | 5:55116260 | ATAAATATAGGAGAC[A/G]GACACAGTGGCACAC | 166979 |
| rs547732452 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB, downstream-variant-500B | CDC20B, MIR449A, MIR449B, MIR449C | GRCh38.p7 | 5:55171972 | AACTAGAATCTCTGC[A/G]TACAGGTCAAAGGAA | 166979 |
| rs547735989 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | CDC20B | GRCh38.p7 | 5:55148260 | GCAATAATTTTTTTG[G/T]GACAATCCCTGGTGT | 166979 |
| rs547947895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55156742 | AGCCGGGCATTTTGG[C/T]GCGTGCCTGTAGTCC | 166979 |
| rs547977952 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55116317 | GTCACTTGAAGCAAG[G/T]TGTTTGAGGCTACAG | 166979 |
| rs548006560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55168080 | ATATTTAGTCCTCTG[C/T]TTGATTTTATCTTTC | 166979 |
| rs548034849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55157395 | TCATCCAATGCTGTC[C/T]AGCGCACAAGTTCTC | 166979 |
| rs548053427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55143856 | CAGTACAGAATCCTA[C/T]CCAGACTGCTGACTT | 166979 |
| rs548057961 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55145636 | TGGAGCCCACTCCCC[A/C]ATCTCTGCCCCAACA | 166979 |
| rs548096464 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55159448 | GAAGTGTTGTTTCTC[A/G]GTTGTGTGTTGTTTG | 166979 |
| rs548117731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55152680 | AACTCTGACAAATCA[A/G]TCTAGTCTAATCCCT | 166979 |
| rs548307034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55114573 | ACAAATTACCACCCA[C/T]TGGGTGGCTTAAAAC | 166979 |
| rs548339895 | snp | C/G | | | upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55173722 | GGCAAGATTTCTATG[C/G]CGATCAAAAGGGAGA | 166979 |
| rs548435638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55129263 | CCCTACAATACATTC[C/T]GTCCCCATGATAAAT | 166979 |
| rs548456357 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55144008 | GGAAAAAAAAAAAAA[A/C]AAACCAGATTTGCAC | 166979 |
| rs548535736 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55149231 | ATAAGCATTGGTAAG[C/G]ATGCGAAGAAACTGG | 166979 |
| rs548601788 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55142980 | TGCCCAAAAGATTTA[C/T]GTCAGACTCCTAAGA | 166979 |
| rs548677111 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55150603 | TAGTTCTTGGTTTTT[C/G]AGTAGGAATGGGAAG | 166979 |
| rs548737400 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CDC20B | GRCh38.p7 | 5:55150046 | GGCTGACAAGAGAAT[C/T]GCTTGAACCCAGGAG | 166979 |
| rs548739267 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55158564 | CACAGAGCGGGAACC[A/G]GAAGAGCAGGCAGCA | 166979 |
| rs548747070 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55151415 | GAAAGGGAGGAGACA[C/T]CGCATTGGAAGATAA | 166979 |
| rs548792082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55134861 | GAAAAGGAAAAACTA[C/T]AGATACAGTAAAAAG | 166979 |
| rs548928257 | snp | C/T | | | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55162143 | GCTCACGCCTGTAAT[C/T]CCAGCACTTTAGGAG | 166979 |
| rs548940081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55133084 | CAAGCTGGGCACATA[A/G]CAAGTAGACCCAATG | 166979 |
| rs549099242 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55134158 | GACCATACTAAGTTC[A/C]AACCACAGGCCGCTG | 166979 |
| rs549153753 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55173617 | CGAGCGTGCACAGCT[C/T]TCCGGCCTCTGTCCG | 166979 |
| rs549174683 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55127461 | TAGTTTTTGTACTAA[C/G]TGAAAACCCAGCACA | 166979 |
| rs549241800 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55155022 | TCCAGGATCTATCTC[C/T]TGCCAAGGAAATGCC | 166979 |
| rs549290554 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55165440 | TTTGTCTAAGAAGAA[A/G]AAGACCCAATTTAAG | 166979 |
| rs549327165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CDC20B, MIR449A, MIR449B, MIR449C | GRCh38.p7 | 5:55172472 | TATGTAATAAGATAC[C/T]AAAATTCTCATATTT | 166979 |
| rs549332527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55143259 | CTTTACCTGTTTGTA[A/G]AGATAAAATAGTTAT | 166979 |
| rs549575303 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55174309 | CTTCATACTGAAAGC[A/C]AGAAAAAATGGCATT | 166979 |
| rs549630071 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55148676 | GCACTCCAGCCTGGG[C/T]GACAAAGTGAGACCC | 166979 |
| rs549784320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55119545 | AGTTCAAAAACTGCC[C/T]AAGATCACCACTCCA | 166979 |
| rs549856275 | snp | A/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55122154 | ACAGGTGAACTTGTT[A/T]TTATAACTGTGATTT | 166979 |
| rs549898696 | snp | A/G | 3.3216e-05 | 0.00407515 | intron-variant | CDC20B | GRCh38.p7 | 5:55119953 | TAGAGAATTCTTGCA[A/G]TTTCTGATTCCTTAT | 166979 |
| rs549917138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55148710 | CTCAAAATAAAAACA[A/G]AAAAAGAAAAAAGAA | 166979 |
| rs550035844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55125405 | TTTGAATATTTCAGA[C/T]TATCTCAACAAAATG | 166979 |
| rs550054569 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55146078 | ATGCAAGTCTCAAAA[A/G]CATATTAAAATTAAG | 166979 |
| rs550060885 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CDC20B | GRCh38.p7 | 5:55156731 | ATACAAAAATTAGCC[A/G]GGCATTTTGGCGCGT | 166979 |
| rs550095296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55115515 | ATCTGGCCCAATCCA[A/G]CAGTGACTTTAATGA | 166979 |
| rs550099006 | in-del | -/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55156177 | AACCATCAGATCTCG[-/T]GAGACTTATTCACTA | 166979 |
| rs550100886 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55149265 | CTTTGTACATTGCAA[G/T]TGTACAGAATGTGAA | 166979 |
| rs550111316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55143849 | CAGAGAGCAGTACAG[A/G]ATCCTATCCAGACTG | 166979 |
| rs550120464 | snp | A/T | 0.000825805 | 0.0203032 | missense | CDC20B | GRCh38.p7 | 5:55133474 | AGTATGGAATCGTTT[A/T]TATCACCAGAACTTT | 166979 |
| rs550120827 | snp | C/G | 0.00478085 | 0.0486577 | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164885 | TCATTTATAAATGAC[C/G]GTATTATAACATTTG | 166979 |
| rs550130528 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55114615 | ATTCTCACAGTTCTG[C/G]AGATGGGAAGTCTGA | 166979 |
| rs550133279 | snp | A/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55123405 | TATATTTATTAATAA[A/T]CATTTTCTTAAATAT | 166979 |
| rs550157064 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55116972 | TGTCGTCTTTATCTC[A/G]GACAAAGGTCCTTTT | 166979 |
| rs550170798 | snp | C/G | | | upstream-variant-2KB | CDC20B | GRCh38.p7 | 5:55174754 | AATCCATGTAAATTG[C/G]GATTTTTAGAATCCA | 166979 |
| rs550187746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CDC20B, MIR449A, MIR449B, MIR449C | GRCh38.p7 | 5:55172535 | ATTTACCAAGAATTC[A/G]TTTGTTCAAGATCAG | 166979 |
| rs550209816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, downstream-variant-500B | CDC20B, MIR449A, MIR449B, MIR449C | GRCh38.p7 | 5:55171889 | GGATTACAGGCATGA[A/G]CCACAGTGCCTAGTT | 166979 |
| rs550248164 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55113099 | CCTGGAGAGGTTAGG[A/G]CTTGTGTGGGTGTGT | 166979 |
| rs550276770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55163961 | AGTCCTAGAACTTGA[C/T]ACTAAAGTTATCATT | 166979 |
| rs550293343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55143701 | AGATAATCACTTTGA[C/T]TGTAGGTCTGGCTGT | 166979 |
| rs550419688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55125919 | AACAAAATTGAGGAT[A/G]AGAGACCACCTTATC | 166979 |
| rs550524358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55146034 | ACATATACATTCATA[C/T]AATCTTTACAAAAGT | 166979 |
| rs550552899 | in-del | -/TG | 0.00279162 | 0.0372561 | intron-variant | CDC20B | GRCh38.p7 | 5:55120609 | AGGTGCACTCATGAA[-/TG]TGTGATGCACTTAGG | 166979 |
| rs550564541 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55162221 | GCCAATATGGTGAAA[A/C]CCCATCTCTATTAAT | 166979 |
| rs550718758 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55140979 | AACATAGTGATAAAT[G/T]ATTAAAGCAGAGAAG | 166979 |
| rs550856318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55133206 | AAAATGTATATTTCC[C/T]ACACCATGCCAACAT | 166979 |
| rs550885498 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55169951 | ACCCCGTCTCTACTA[A/C]AAATACAAAAAAATT | 166979 |
| rs551056751 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CDC20B | GRCh38.p7 | 5:55139325 | CCAGAAAGAGCACAA[C/T]ATAGCTGCCCAAAAA | 166979 |
| rs551087196 | in-del | -/A | | | intron-variant | CDC20B | GRCh38.p7 | 5:55143996 | TTATCTCTGTATGGA[-/A]AAAAAAAAAAAAAAA | 166979 |
| rs551115795 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55166604 | CATAGGAATACCAGC[A/G]GACAAACACATAGAG | 166979 |
| rs551231081 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CDC20B | GRCh38.p7 | 5:55148578 | AATGAGTTGAGCGTG[A/G]TGGTGTGTACTTGTA | 166979 |
| rs551282568 | snp | C/G | 1.67075e-05 | 0.00289023 | intron-variant, upstream-variant-2KB, nc-transcript-variant | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170699 | GGCTGCTGACTTGAC[C/G]CAAGCAGCCAGCTAA | 166979 |
| rs551313505 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CDC20B | GRCh38.p7 | 5:55147950 | TTCTCTAAGAAACAC[C/G]AGGAGTTTGATATTT | 166979 |
| rs551330850 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CDC20B | GRCh38.p7 | 5:55125136 | AAGACCCCTAGGACA[G/T]ATTCAAAACACAGGT | 166979 |
| rs551341380 | snp | A/G | 0.000199286 | 0.00998014 | intron-variant | CDC20B | GRCh38.p7 | 5:55127398 | ATTGGAGTTTTCACA[A/G]CCCACTGTCTTCTCA | 166979 |
| rs551485584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55141563 | ATACTCACTGAGTCA[C/T]GAAGAATGTAAACAT | 166979 |
| rs551546777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55141083 | ACGCCAAAGGTCATG[C/T]TGAGGTCTGGAGGGA | 166979 |
| rs551553929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55162265 | GCCAGGTGTGGTGGT[A/G]GGCACCTGTAATCCC | 166979 |
| rs551557728 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55171459 | CAAAACTGCAGCAGT[A/G]TTTGGGGGAAAAAAT | 166979 |
| rs551565740 | snp | C/G/T | 4.32715e-05 | 0.00465126 | intron-variant, upstream-variant-2KB | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170772 | GGCCCAGGCAGTCAC[C/G/T]GAGGCTAAATTTGTA | 166979 |
| rs551606333 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | CDC20B | GRCh38.p7 | 5:55120012 | ATGCACTGTCCATGA[A/C]CCAACCTCCAGTACA | 166979 |
| rs551644627 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55122410 | CCAAAGTGCTGGGAT[C/T]ACAGGCATGAGCCAC | 166979 |
| rs551707484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55134691 | CACTTGAGCCAGGAG[C/T]GCCACTCCACATCAG | 166979 |
| rs551979234 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55134376 | GAAAACCTGTAGCTG[A/G]GGGCAAAACTGCAAG | 166979 |
| rs552021407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55118913 | TCACTACCTAACATT[A/G]CATATATTTGTTTTC | 166979 |
| rs552022104 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160484 | TTTTTTGCTGTTACA[C/T]GGTCATAAGTTGGAA | 166979 |
| rs552035167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55139432 | TCTGAAAGGGAGGAC[A/G]TCAAGGAAAAGAAGA | 166979 |
| rs552135856 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | CDC20B | GRCh38.p7 | 5:55119368 | AACGAAGCTGAGAAG[A/C]GTAGTGGTCTACCTT | 166979 |
| rs552170277 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55124034 | ACATATATTCTGGGA[A/C/G]TACGTTGAGGTCAAG | 166979 |
| rs552201513 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55169016 | GCTCTTTAATTTAAA[A/C]AAACTAACACACAAA | 166979 |
| rs552213577 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55168154 | CCACCACACTCCTTC[C/G]CACTCTTCCCTTCCC | 166979 |
| rs552246909 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55150794 | CTGTCACCTAGGCTG[C/G]AGTGCAGCGGCACAA | 166979 |
| rs552307611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55153602 | TAGCCTGAATAAATC[C/T]CCCCGGGGTGGACTG | 166979 |
| rs552371214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55161396 | AGAGCCAGAATCTCA[C/T]CCTTTGTAACTTCTA | 166979 |
| rs552416303 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55114613 | TGATTCTCACAGTTC[C/T]GGAGATGGGAAGTCT | 166979 |
| rs552456428 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55115407 | TCGGAGATGAGGCAA[C/T]AACAGGCAGTACTTC | 166979 |
| rs552548961 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55149770 | GTGATGAAAACATTT[G/T]GGAACAAGAGAGAAG | 166979 |
| rs552639224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55130054 | TTCTCCATGAAGTGA[A/G]GAAAAACACACATGA | 166979 |
| rs552687944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, missense | CDC20B | GRCh38.p7 | 5:55137609 | TCCTCCTGTTCAAAT[C/T]GTTTCTTCATGCTGC | 166979 |
| rs552703758 | snp | G/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55141058 | CAAACACTGTGTCAG[G/T]TTCAGAACTACGCCA | 166979 |
| rs552712497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55131318 | TCCCTAGAAAAATGA[C/T]GACAAAACACAATAC | 166979 |
| rs552828652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55130797 | TTTAAAACGTTTACA[A/G]TTGGATGGTTTTCAG | 166979 |
| rs552853966 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55139549 | ATAGTTATCTAGTAA[A/G]TGAAAACTAAGGCAA | 166979 |
| rs552883936 | in-del | -/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164284 | GTCTCATTTTAAACA[-/T]TTTTTTTTTTGGAGA | 166979 |
| rs552898620 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CDC20B | GRCh38.p7 | 5:55132002 | TTAAACCCAGGAGGC[A/G]GAGGCTGCAGTGAGC | 166979 |
| rs552956888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55153011 | GGGGAGGCCAAGGCA[A/G]GTGGATGGCTTGAGC | 166979 |
| rs553008460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55138524 | AGAACTAAGCTCTTT[A/G]CCCTAGTACTATTTT | 166979 |
| rs553019754 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55152133 | GGCAGTCACCAGAAA[A/C]CAGAAGAGGCAAGGA | 166979 |
| rs553020141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160653 | TTTGGAAAATACTTA[C/T]AGTTAGTAATGTGAA | 166979 |
| rs553058309 | snp | C/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55133164 | AATAGACCATCATTA[C/G]TACAATTCTTTCTAA | 166979 |
| rs553170898 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55169306 | AAATAAGGAAAGCAT[A/G]AAAATTATTTTACCA | 166979 |
| rs553307409 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55150334 | TAGCTCTAAATGAAA[A/G]ATAGGAAGGGAATAT | 166979 |
| rs553364743 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55136752 | AAATGAACCACGCTA[G/T]TTCTCTCAAGAGGAT | 166979 |
| rs553391454 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55128855 | ACACTGAAATATATT[G/T]ATTTAGAGCCATTTA | 166979 |
| rs553421882 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55166333 | AGCCAGATAAAGTGG[A/G]TTTCTTCACTTACAT | 166979 |
| rs553465687 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55121182 | TTAACAAATACTACA[C/G]TTATATGTATCTGTG | 166979 |
| rs553467341 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55130128 | GATAAACAGAAAAAT[C/G]AAAAGTATTTTCTAA | 166979 |
| rs553523256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55168404 | CCTCTTTTTACCATC[C/T]CTTTTCCCTCTGCTT | 166979 |
| rs553560539 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55158020 | GACATGAACACATCC[A/C]CTATGGAAAACAAAG | 166979 |
| rs553610020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | GPX8, CDC20B | GRCh38.p7 | 5:55167492 | TTGCCAGCTCAATGT[A/G]AATGCTCATGCTCCC | 166979 |
| rs553624594 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55157932 | GTATTCTATGAATTA[A/G]TTTTAAAATGCATGT | 166979 |
| rs553666042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55116462 | TTTATTTATTTATTT[A/G]TTTTGAGACAGGGTC | 166979 |
| rs553758365 | snp | A/G | | | upstream-variant-2KB | CDC20B | GRCh38.p7 | 5:55174422 | ATCAAAATGTTTGAT[A/G]GTCAAATAACTAGTG | 166979 |
| rs553762933 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55141388 | TCTTTCTCCAGGTGC[C/T]AGCTTCTGCACAGTG | 166979 |
| rs553810827 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55122654 | ATTAGGTTATATTAA[C/T]AAAAGGTGTTAACGC | 166979 |
| rs553818054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55143760 | AAAGCCCAGGCTCTC[A/G]TCACTCCAAAGTCCA | 166979 |
| rs553886154 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55141301 | AGCTTAACACTTTCT[C/T]TCTCTGGGCACGAGC | 166979 |
| rs553908214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55134350 | TAAATTCCTGCTTCC[A/G]TGTTAGCTATGAAAA | 166979 |
| rs553967850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55142006 | AATGGCCTGCTCATC[A/G]GTAGTTCAATGAACT | 166979 |
| rs554011289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55148860 | GCAGATCTTATTTAC[A/G]CCCATTTTATCAGTG | 166979 |
| rs554091867 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55135156 | ACAAGGGATATAAGG[C/G]AACCTGCACCTTCTG | 166979 |
| rs554093340 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CDC20B | GRCh38.p7 | 5:55125968 | AAATGAAATTACACA[C/T]ATAAAAAGTATAGCA | 166979 |
| rs554136308 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55127549 | CACTATGGATGCTGA[A/T]TTAGTTGGTAGAGTA | 166979 |
| rs554269617 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55166409 | GTGCTGGATTTTCTC[C/T]CCTTGCCCTTTAGGT | 166979 |
| rs554273793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55150377 | AAGCAGTAAGCATTG[A/G]TTCAGTTTGGGTTTT | 166979 |
| rs554422445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55144201 | CTCCCCCTTTCTATT[A/G]CAGAAAGATGTTTTA | 166979 |
| rs554538197 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55167115 | GCTGTCGTTCTTGTG[A/G]AAAAGGAAAAGGACA | 166979 |
| rs554545587 | snp | A/C | | | utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55113011 | AACAGCTATAATAGT[A/C]TAATAATACCAAATA | 166979 |
| rs554552933 | in-del | -/AA | 0.00835141 | 0.0640778 | intron-variant | CDC20B | GRCh38.p7 | 5:55158067 | TGTTGCTCTGAAACC[-/AA]AAAAAGTTTGAGGTC | 166979 |
| rs554581087 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55169752 | GGAAAATTACCTCAA[C/T]TTTCCCTTCAGTTGG | 166979 |
| rs554703516 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55141587 | TAAACATCCTACCTC[A/G]GCCTATCCTTGACCA | 166979 |
| rs554743304 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | CDC20B | GRCh38.p7 | 5:55135250 | ATATATATATATATA[A/C]AGAGAGAGAAAGAGA | 166979 |
| rs554823167 | snp | C/T | | | intron-variant, upstream-variant-2KB, downstream-variant-500B | CDC20B, MIR449A, MIR449B, MIR449C | GRCh38.p7 | 5:55172066 | GCTCTTTATGAAACA[C/T]GTTTATAAAACCATT | 166979 |
| rs554891218 | snp | C/T | 1.86086e-05 | 0.00305024 | intron-variant | CDC20B | GRCh38.p7 | 5:55128669 | AGCCACATGAAAACA[C/T]GTTCAAATAAACAAC | 166979 |
| rs554903787 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55142090 | CAAGGTTTAGCAGGC[A/G]CTTCTGTTCTGTGGG | 166979 |
| rs554929340 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC20B | GRCh38.p7 | 5:55174812 | ATCATTCATTTAGAA[C/T]GCAATTATCTGTAAA | 166979 |
| rs554947008 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant | CDC20B | GRCh38.p7 | 5:55121786 | CAAAACAGATTATAA[-/G]GGTAATTTATTTTCT | 166979 |
| rs555015907 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55156827 | TGCAGTGAGCCGAGG[A/T]TGCACCACTGCACTC | 166979 |
| rs555020284 | snp | A/G | 0 | 0 | intron-variant | CDC20B | GRCh38.p7 | 5:55149080 | AGAACTGACTAGGCA[A/G]ACTAACAGGACATCT | 166979 |
| rs555027641 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55153109 | CTGGGCACGGTGGTG[C/T]GTGCCTATAGTCCCA | 166979 |
| rs555087845 | in-del | -/TC | 0.00318978 | 0.0398085 | intron-variant | CDC20B | GRCh38.p7 | 5:55145864 | TCATTCTCTCCTGCT[-/TC]TGTCTTTTTCTTCCA | 166979 |
| rs555121774 | snp | G/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55173907 | AAGGCGTGAAGAGGG[G/T]GCCAGAAAGCTGAGC | 166979 |
| rs555296556 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55120066 | TTACAACCATTCTAG[G/T]AAAGTTTATCCCAAG | 166979 |
| rs555365615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55133590 | TAATATTTATTCTTG[C/T]GGGAATTAAGAAATA | 166979 |
| rs555401995 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55119673 | AGGGTGGATGTAGGA[C/G]TTTTTCCTCTGATGA | 166979 |
| rs555410863 | snp | C/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55113450 | AGTTGATGAGCAGGG[C/G]ACTGAGAGGATCAGC | 166979 |
| rs555467013 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CDC20B | GRCh38.p7 | 5:55153954 | TGTAAAAAATCAGTA[C/T]GATTTTAGGTCCCAT | 166979 |
| rs555470333 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55171018 | AAATGAATTTTAAAA[C/G]TTACTTAACTGTAGG | 166979 |
| rs555540057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55163364 | CTGCCAAAAAAAAAG[C/T]TATTGCTTTTCAAAA | 166979 |
| rs555550793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55126145 | AGTTGTTTTAAGACC[A/G]GCCAAAAACACAAGA | 166979 |
| rs555639993 | snp | C/T | | | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160693 | ATTTATTAATAAAAG[C/T]ATTGGTTCTATAATC | 166979 |
| rs555708610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55118279 | AGAAATACTGTATGT[A/G]GAAGAAACTAATGGG | 166979 |
| rs555725932 | snp | C/G/T | 4.4932e-05 | 0.00473966 | synonymous-codon, upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55172977 | GACCCTCCGAGGCGC[C/G/T]GTGCGCTCCAGTTTC | 166979 |
| rs555760095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55141126 | GCAGAAAGAACACTT[C/T]GGGGGGCCGTAGGCA | 166979 |
| rs555815522 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55173632 | CTCCGGCCTCTGTCC[A/G]TTGGTAATCGCTGTG | 166979 |
| rs555825569 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55124080 | CAAGTCCTCAAGAAG[A/G]AAACTATGGAATTTT | 166979 |
| rs555880438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55147145 | TATGTTGTTTTATAT[A/G]TTTATATATTATATA | 166979 |
| rs556001209 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55126454 | CCTAGGTGACAGAGT[A/G]AGATTCCATGTCAAA | 166979 |
| rs556065050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55140536 | CCACATTGTCAAAGC[C/T]AACACCACAATAATC | 166979 |
| rs556199725 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164397 | TTAAATGTGGCAATG[A/G]AGGATTTTTTTTTAA | 166979 |
| rs556251112 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55121133 | TTTATATTGATAATT[G/T]AAATTACTAATAATA | 166979 |
| rs556269447 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CDC20B | GRCh38.p7 | 5:55116637 | AATTTTTCTAGAAAT[C/G]GAGTCTCACCATGTT | 166979 |
| rs556273047 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CDC20B | GRCh38.p7 | 5:55147424 | TGTTATATTTTATAT[A/T]TTTTTATATTGATAT | 166979 |
| rs556295649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55141195 | CTTTCTTACACTAGC[C/T]CTCTACACTGTTCAC | 166979 |
| rs556307422 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55141428 | CAATTATACCTTTTA[C/T]GGACAATAGTGGCTT | 166979 |
| rs556331209 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55156445 | GAAGTCGAAAGTTCA[A/T]AACTCTATTCTTCAT | 166979 |
| rs556347440 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55150109 | TGCACTCCAGCCTGG[A/G]CAACAAGAGTGAAAC | 166979 |
| rs556386083 | snp | G/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55156486 | ACTAATTCTGTGATC[G/T]TGGCTGAGTTAACTG | 166979 |
| rs556482870 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CDC20B | GRCh38.p7 | 5:55141930 | TAGATATTGCCAAAT[A/G]CCCCTTGGTGAGTAA | 166979 |
| rs556517203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55154510 | TGACAGAGTGAGACC[A/G]TGTCTCCCAAGAAAA | 166979 |
| rs556528740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55149474 | CAACAGATGAATGCA[C/T]AAACAAATCATGGGA | 166979 |
| rs556531595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55162635 | TGATATAATGCCTAA[C/T]GCCATAAATGGCAAC | 166979 |
| rs556719297 | snp | C/G | 1.64876e-05 | 0.00287116 | missense | CDC20B | GRCh38.p7 | 5:55124982 | TTCCAACATGATGCT[C/G]GGCTACCCGAACATC | 166979 |
| rs556785178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55126225 | CTTTGGGATGGCCAG[A/G]CGCGGTGGCTCACAC | 166979 |
| rs556882525 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CDC20B | GRCh38.p7 | 5:55125491 | TAACAGGTAGAGTCC[C/T]ATTAACCTATAGATC | 166979 |
| rs556949309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55146229 | TCAGTCAATCACAGG[C/T]GGCCAACTAATCAGA | 166979 |
| rs557012102 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55145937 | TGACTCTGTATACCA[C/G]TAACCTTACCAGTCA | 166979 |
| rs557061926 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55139604 | ATACTAGAAAAGAAG[C/G]ATAATTATATTATTT | 166979 |
| rs557133132 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55116585 | TCTCAAATAGCTGGG[A/T]CTATAGAGTGTGCCA | 166979 |
| rs557179674 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CDC20B, MIR449A | GRCh38.p7 | 5:55170132 | AAAAAAAAAGAAAGA[A/C]ACTAATAATGCAGAA | 166979 |
| rs557265318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55171142 | AACATGGTGAAACCC[C/T]GTCTCTATTAAAAAT | 166979 |
| rs557296513 | snp | G/T | | | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55163388 | TTCAAAATAAGGTGA[G/T]TATTCACTTTGGGAG | 166979 |
| rs557308571 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55130261 | AATTCCTTGGATACA[C/G]TGAATAGCAGGATAG | 166979 |
| rs557412390 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | CDC20B | GRCh38.p7 | 5:55151840 | ATTAGGCAGCCAATG[A/G/T]TAGCTAAATAATGGT | 166979 |
| rs557440698 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CDC20B | GRCh38.p7 | 5:55128946 | TAAAAGTTAAAAGCA[C/T]ATAATTCTTATGGAG | 166979 |
| rs557452430 | snp | C/T | | | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55161652 | TTATTAGTTAACATA[C/T]GTTTGTGGCTAATTT | 166979 |
| rs557532369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55169365 | TGCGAAATATTTCTT[A/G]TATCTCATCTATGGC | 166979 |
| rs557586417 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | CDC20B | GRCh38.p7 | 5:55130041 | AGCAGCCATTATATT[A/C]TCCATGAAGTGAAGA | 166979 |
| rs557609986 | snp | A/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55130825 | CAGTGTATGTAAATA[A/T]AAAATGCATGACAGG | 166979 |
| rs557746617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55132187 | TTGGTCATGACAATA[C/T]ATTCTCTTGGAGAAG | 166979 |
| rs557746758 | snp | A/G | 3.58764e-05 | 0.0042352 | intron-variant | CDC20B | GRCh38.p7 | 5:55140432 | AACACACATAAGGAG[A/G]ATATTTCTTTAAAAA | 166979 |
| rs557798588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55169983 | GCCGGGCATGGTAGC[A/G]GGCGCCTGTAGTCCC | 166979 |
| rs557800786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55125569 | AAAACCAATTGAATG[C/T]CACAGCAAACTGCAA | 166979 |
| rs557807798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55119634 | GGCAAATTCAGAAAC[A/G]TTCAACTATACGCTC | 166979 |
| rs557890674 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | CDC20B | GRCh38.p7 | 5:55149601 | AAGTGAAAGAAGCCA[G/T]ACAGGAAAGGTCACA | 166979 |
| rs557913919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55119136 | TATAATCAGAGTTCT[A/G]CAAGAGATTGGATGC | 166979 |
| rs557967696 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB, downstream-variant-500B | CDC20B, MIR449A, MIR449B, MIR449C | GRCh38.p7 | 5:55171988 | TACAGGTCAAAGGAA[A/G]ATGAACTATTGAGCC | 166979 |
| rs558064840 | snp | G/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55151321 | GACTCAACAGAGCAT[G/T]TCTGTGGGCCACATT | 166979 |
| rs558079510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55153158 | GTGGGAGGATGGCTT[A/G]AGCCCAGAAGGCAGA | 166979 |
| rs558112792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55124260 | ATCTCTCTGGCCACA[A/G]TTATTAACTGAGAGA | 166979 |
| rs558239679 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55118115 | CAGAGTGAGACTCTG[C/T]CTCAAAAAAAATAAA | 166979 |
| rs558283179 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55169434 | ACTGGCTGCAAATGT[C/T]CGCACAAGAATACTG | 166979 |
| rs558327715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55117607 | TGTTCTTGACCCACA[A/G]TGGAAACACAGCCTC | 166979 |
| rs558371046 | snp | C/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55133248 | TCCCTAAATATGAAA[C/G]TTGCACCAGGAAAAG | 166979 |
| rs558580000 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55130294 | GTGATAGAGGAAAGA[C/G]TAAACTTGAATATAG | 166979 |
| rs558604170 | snp | C/T | | | intron-variant, downstream-variant-500B | CDC20B | GRCh38.p7 | 5:55136446 | GGCCTGTAATCCCCA[C/T]TATTCAGGAAGCTGA | 166979 |
| rs558671513 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55141191 | ACAGCTTTCTTACAC[C/T]AGCTCTCTACACTGT | 166979 |
| rs558707231 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CDC20B | GRCh38.p7 | 5:55122134 | TTTTGCCAAACCTGT[C/T]TATGACAGGTGAACT | 166979 |
| rs558744628 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55146387 | TCTTTGCACAATTAA[C/T]TTTGTAAAATTTAAT | 166979 |
| rs558749926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55128717 | AAGAATAATACCATC[C/T]CCATGGTTAGCTGGA | 166979 |
| rs558780904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55115874 | TGTCCACGTGCATGC[A/G]CAAGCACACACACAC | 166979 |
| rs558864345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55114935 | TTTAGCATGGGTATC[C/T]TTTAGGAGACCATTT | 166979 |
| rs558869723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55135357 | TTTATTCTAAGCCAA[A/G]TACTCAGCACCTTAC | 166979 |
| rs558938027 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CDC20B | GRCh38.p7 | 5:55116420 | AAAGAAGAGGATAAA[C/T]ATATAATAGAACATT | 166979 |
| rs559117015 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55161865 | AGGTCATGAGGCATA[C/G]AGACAGCATAGGCTT | 166979 |
| rs559129976 | snp | C/G | | | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55159086 | GCAGTCTACAAACAC[C/G]ACTCACTGCAGCCTC | 166979 |
| rs559144013 | in-del | -/ATACT | 0.00199481 | 0.0315187 | intron-variant | CDC20B | GRCh38.p7 | 5:55123025 | TAGATAACCAGACAG[-/ATACT]ATAAACAGAAACCTT | 166979 |
| rs559157774 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55123355 | CCCCTGAGCCCATGG[G/T]CCCCAGTTTTACCAT | 166979 |
| rs559176259 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55166487 | CTTGAAAGAAAGGAC[A/G]TTCAGGTGTCCCTTC | 166979 |
| rs559185298 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160091 | TAGCAGTGAAAGCAG[C/T]CAGCCTGTCCTTCCT | 166979 |
| rs559239390 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | CDC20B | GRCh38.p7 | 5:55174855 | AATTCCATTATAGCC[A/G]TTAATTCCACAGCAT | 166979 |
| rs559257151 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55131840 | GAGGCCAAGGCAGGC[A/G]GATCACTTGAGGTCA | 166979 |
| rs559263900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | GPX8, CDC20B | GRCh38.p7 | 5:55167366 | TCAATAGTATATATA[C/T]GTGTACATATATATA | 166979 |
| rs559267064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55116275 | GGACACAGTGGCACA[C/T]GCCTGCAGTCCCAGC | 166979 |
| rs559323500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55167945 | GCTGAGGTGAGAGGA[C/T]TGCTTAAGCCCAGGA | 166979 |
| rs559347097 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55117629 | CACAGCCTCACAACG[A/T]AAGCCATAAAAATTA | 166979 |
| rs559487476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55123905 | ACAATGTAGTGGCAG[C/T]AGTCACTATATATTT | 166979 |
| rs559527403 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55174058 | AAGAGAGCCGAGTTG[C/T]GCCATATGGCAGGAG | 166979 |
| rs559616592 | snp | G/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55157926 | CAGCAGGTATTCTAT[G/T]AATTAATTTTAAAAT | 166979 |
| rs559679799 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | CDC20B | GRCh38.p7 | 5:55175010 | TGGAAACAGAAACTC[A/G]CCACTTGGCAAATAT | 166979 |
| rs559681188 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | CDC20B | GRCh38.p7 | 5:55150483 | GCTGCTCTGTGCTCT[A/C]CCCACCAGCTGACCA | 166979 |
| rs559707808 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CDC20B | GRCh38.p7 | 5:55156641 | AGCACTTTGTGAGGC[C/T]GAGGCGGGCAGCTCA | 166979 |
| rs559718403 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CDC20B | GRCh38.p7 | 5:55155948 | AAAACAAAATGCCTC[C/T]TCACGAATGAAACCC | 166979 |
| rs559722312 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164531 | CTTCCTCTGACCATA[C/T]TAAAGAATTCAGAAT | 166979 |
| rs559758238 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55166123 | GAACTCATAGCAGTG[C/T]TGTGGCACTGCAGGG | 166979 |
| rs559777113 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55152423 | CCTGGGATATATGAA[C/T]CGGAGGGAGTGTCTA | 166979 |
| rs559798864 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | CDC20B | GRCh38.p7 | 5:55122285 | TCTCTTTTTTTTTTT[C/T]TTAAGACACAGTCTC | 166979 |
| rs559937412 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55171467 | AGCAGTGTTTGGGGG[-/A]AAAAAATCAACATTA | 166979 |
| rs559989464 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55158482 | AGAGTAGGAGTCGAG[C/T]GGTTCCTCTCACAAG | 166979 |
| rs560018478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55149223 | GGAAACTAATAAGCA[C/T]TGGTAAGGATGCGAA | 166979 |
| rs560048063 | in-del | -/ATTTA | 0.00119737 | 0.0244387 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55162600 | TTCTAAAAACATTAT[-/ATTTA]ATTTCTAGGGAAAGT | 166979 |
| rs560049726 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55117076 | TAGTCATAAATGAGA[C/T]CACATATTGATACAT | 166979 |
| rs560166671 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55113617 | TGAGGAAGCACAGAG[C/G]AGAATAATCAGGAGG | 166979 |
| rs560295339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55147490 | TAAAACATGTTATTT[C/T]ATATGTATTTATATA | 166979 |
| rs560322101 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55173954 | GATAAAGGGGGAGAG[A/G]AAGATATTGAGGGTT | 166979 |
| rs560338918 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55133800 | TAGAAGATAGATCTT[C/G]TGAGGAGTACACAGA | 166979 |
| rs560341382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55134738 | AGGTTCTGTCTCTAA[A/G]AAAAATAAAAAATAA | 166979 |
| rs560353301 | snp | A/G | | | downstream-variant-500B | CDC20B | GRCh38.p7 | 5:55112833 | AAAATTCATGTCAAA[A/G]CAAAAAAAAATAATC | 166979 |
| rs560357340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55171503 | TTTAAGAAATGTAAG[A/G]GCTTAAATGCAATTA | 166979 |
| rs560508726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55126267 | GCACTTTGGCAGGCC[A/G]AGGCAGGTGGATCAC | 166979 |
| rs560555463 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55157171 | ATTTACTGAAAGAGC[A/G]CTGGTGGTTTTTCTA | 166979 |
| rs560555556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55149249 | GCGAAGAAACTGGAA[C/T]CTTTGTACATTGCAA | 166979 |
| rs560637442 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55158557 | CACATGCCACAGAGC[A/G]GGAACCAGAAGAGCA | 166979 |
| rs560717928 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55167017 | CCTGGGCAACAGAGC[A/G]AGACCCCATCTTAAA | 166979 |
| rs560724987 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55119460 | CTTGCCCTTTCAGAT[C/G]GCTTTATCTTCCACC | 166979 |
| rs560809177 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC20B | GRCh38.p7 | 5:55175138 | CTGGCCAAAACTGGC[A/G]GAGACCACCTTAACC | 166979 |
| rs560814332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55134095 | GGTTAATTTTACCCA[C/T]GACTATCTAAGGTCA | 166979 |
| rs560850121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55143133 | CAACTTTTCCTAAGA[A/G]ACCCCAAAGGACAGA | 166979 |
| rs560858700 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55165909 | GTTTTAAGTGACCAG[G/T]AAGGAAATCAGAACT | 166979 |
| rs561056429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55126364 | ATTACCCAGGCATGG[C/T]GGTGGGCGCCTGTAG | 166979 |
| rs561093195 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | CDC20B | GRCh38.p7 | 5:55136216 | CTCCCAAAGTGCTGG[G/T]ATTATAGGCGTGAAC | 166979 |
| rs561138168 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55122417 | GCTGGGATTACAGGC[A/C]TGAGCCACTGCACCT | 166979 |
| rs561142598 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55141318 | CTCTGGGCACGAGCA[A/C]GCCAAGCTGTGTCCT | 166979 |
| rs561155941 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CDC20B | GRCh38.p7 | 5:55143789 | CATTGCAGAGAGCAG[A/G]ACAGAGTGAAAAAGC | 166979 |
| rs561213208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55156691 | CCAGCCTGACTAATA[C/T]GGTGAAACCCCATCA | 166979 |
| rs561279589 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55139653 | AGTTGTGTAGTAATA[C/T]GATGTAAACATTAAC | 166979 |
| rs561370450 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55173246 | GGAATCCCCCTCGCC[G/T]GCTTCTTATTGGCCG | 166979 |
| rs561393836 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | CDC20B, MIR449A, MIR449B, MIR449C | GRCh38.p7 | 5:55172479 | TAAGATACTAAAATT[C/T]TCATATTTTCAGACC | 166979 |
| rs561394481 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55131628 | AATGAGGAGTTCTTT[A/G]GTAATGTTTGGAAGA | 166979 |
| rs561404136 | snp | C/G | 1.65241e-05 | 0.00287433 | intron-variant | CDC20B | GRCh38.p7 | 5:55119929 | CAAATCTGTAATAAT[C/G]ATCAAAAATAGAGAA | 166979 |
| rs561504696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55171303 | GGGCAACAAAGTGAG[A/G]CTCTGTCTCAAAAAA | 166979 |
| rs561563817 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55142048 | CACTTCTTTAGAATC[C/T]CACAGTTACCACAAA | 166979 |
| rs561592697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55162870 | GTCATTCCACTTAGA[C/T]AGGAAGGATCATAGA | 166979 |
| rs561593018 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55165677 | ATTTGGTGGAGGTGG[A/C]ATTTCTACCAGAGGT | 166979 |
| rs561709933 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55118680 | GAGGATTGACTCATG[A/C]TCTTCCTACACTTGC | 166979 |
| rs561723920 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55156267 | CCCTTCATATGTGGG[A/G]ATTATTACAATTCAA | 166979 |
| rs561733557 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55154276 | ACTCTAAGCATTTTG[C/G]GGGGCCAGTGCAGAG | 166979 |
| rs561869330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55155045 | GAAATGCCTGTCGCA[C/T]AGTTTTGAATGACTC | 166979 |
| rs561913142 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CDC20B | GRCh38.p7 | 5:55147518 | ATATAAAAATGTTAC[A/G]TATTTTTATATATTT | 166979 |
| rs561927867 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55145588 | GGGGCTCTGGCAGGT[A/T]GATCATGGATCCTGC | 166979 |
| rs561994466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55148453 | CCGTGGCGGCTCATG[C/T]TTGAAATCGTAGCTC | 166979 |
| rs562046708 | snp | A/T | | | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55158675 | ACTTTCTGGAAACAC[A/T]TCATGATCAAATGGC | 166979 |
| rs562068667 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55150452 | CCCAGGGGGCGAGGC[C/T]GGCTCTCTCTCCACT | 166979 |
| rs562093653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55139747 | GCAGGAAGAGAACTA[A/G]ATTCTTATCTACTAT | 166979 |
| rs562136263 | snp | C/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55165257 | CTTAGAGTCACAAGG[C/T]ATTTCTTCTCCCAAA | 166979 |
| rs562193079 | snp | C/G | 0.000292869 | 0.0120975 | intron-variant, upstream-variant-2KB, nc-transcript-variant | CDC20B, MIR449A, MIR449B, MIR449C | GRCh38.p7 | 5:55172280 | TCTGAATGCAACAGA[C/G]AGGAGTGCAACTAGC | 166979 |
| rs562216180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55131626 | ACAATGAGGAGTTCT[C/T]TGGTAATGTTTGGAA | 166979 |
| rs562321840 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55151673 | TGTGATTCGTCTACC[A/G]TCACTCTGTCCACCC | 166979 |
| rs562332249 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55163632 | CTGTCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 166979 |
| rs562359182 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CDC20B | GRCh38.p7 | 5:55142550 | GGAAGTCTTAAGGGG[C/T]AGGGCAGCAAAAACT | 166979 |
| rs562451334 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55119740 | TCATTCAGGGCTTTT[A/C]CCCCCAACAACAGCT | 166979 |
| rs562491453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55155232 | CAGTGCCAAAAATAA[C/T]TAGAAAAGGACCCAG | 166979 |
| rs562526159 | in-del | -/AA | | | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55162112 | AAAAAAAAAAAAAAA[-/AA]GGCCGGGCGCGGTGG | 166979 |
| rs562531866 | in-del | -/AA | 0.184838 | 0.241358 | intron-variant, downstream-variant-500B | CDC20B, MIR449A | GRCh38.p7 | 5:55170113 | GCGAGACTCCGTCTC[-/AA]AAAAAAAAAAAAGAA | 166979 |
| rs562548314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55162951 | CCTGGCTCAACCACT[C/T]ATTAGCCACGTGACC | 166979 |
| rs562618309 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | CDC20B | GRCh38.p7 | 5:55112919 | TAACGCATGCTCCCT[C/G]AAGCCCTCAATTCAA | 166979 |
| rs562669120 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55141536 | ACAAGTGGAGTTATA[C/T]GCCTGTGCTCTATAC | 166979 |
| rs562762379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55140651 | CTCCATAGAGCAGGT[A/G]TTTTTTGGCTAGAAT | 166979 |
| rs562792488 | in-del | -/TTTT | | | intron-variant, upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55172772 | TTTTTTTTTTTTTTT[-/TTTT]GGCAACTAGGCACCT | 166979 |
| rs562805033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55142175 | AATATGGAGCTCCTG[A/G]AAGATGAATTCTGAA | 166979 |
| rs562834432 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55133993 | ATATTTCAGTATTGG[A/G]GCACACAGACTCCAA | 166979 |
| rs563015163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55124522 | TGATATTTAAAACCA[A/G]CTGTATGTACCCAGG | 166979 |
| rs563031886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55140010 | CCAGCCTGAGCAACA[C/T]CAAAAACAAAAAAGT | 166979 |
| rs563050931 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55123952 | GCCCTGTAATAACTT[A/T]TAAATCCTCTTGTAA | 166979 |
| rs563086140 | snp | A/T | | | intron-variant, downstream-variant-500B | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170295 | TCCAAAGACTCCAAA[A/T]ATATTTCTTAAAAAT | 166979 |
| rs563093457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55135246 | GTCTATATATATATA[C/T]ATACAGAGAGAGAAA | 166979 |
| rs563116575 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55132405 | TCTTTCAACTACCAG[A/C]ATTCGTTTCAAATAA | 166979 |
| rs563198488 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55168960 | ACCTGCACATGTACC[A/C]CCTGGATCTAAAATA | 166979 |
| rs563282734 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | CDC20B | GRCh38.p7 | 5:55131382 | AAATAGAACAGAAGT[A/T]AAAAAAGAAAAGATG | 166979 |
| rs563412100 | in-del | -/A | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55115137 | TAATGAAAAAGGACC[-/A]AAAAAAGCTCTCCCA | 166979 |
| rs563424916 | snp | A/G | | | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55161985 | AATGGGCTATCAATA[A/G]TACCGCCTTCTTAAG | 166979 |
| rs563507682 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55117315 | GTAAAGGTGTGACCA[A/G]AATCTAGAATAGTTT | 166979 |
| rs563507766 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55157678 | TCACAAGCAAGTTTG[C/T]AACAGCATAATTTTG | 166979 |
| rs563515345 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55115336 | TTAAGAAAATTAAAC[A/T]TTTCCTTATTTCAGG | 166979 |
| rs563516827 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55158678 | TTCTGGAAACACATC[A/G]TGATCAAATGGCATA | 166979 |
| rs563531059 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55158182 | GGGGCCCAAAATGCT[A/G]TGTTTCTAACAAATG | 166979 |
| rs563549068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55169779 | TTGGTACACACACAG[C/T]CATGGCTATAGAAAC | 166979 |
| rs563580320 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55166744 | GAAAAATATCAACAT[C/T]AGAGCCTGGCACAGT | 166979 |
| rs563657871 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55123186 | GAATGTAATGTTTTC[A/T]GTCAAAATAAAATAT | 166979 |
| rs563685436 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | GPX8, CDC20B | GRCh38.p7 | 5:55167727 | AATTAGCTGGGTGTA[G/T]TGGCACATGCCTCAG | 166979 |
| rs563841745 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55117848 | GGCCAGGCATGGTGG[C/T]TCATACCTATAATCC | 166979 |
| rs563867839 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55144709 | GCCAGCTCTCAGAAC[G/T]TCAAATGAGAAAGAA | 166979 |
| rs563868171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55152258 | AACTAGAAGAGAATA[C/T]GTGTGTCTAAGCTAC | 166979 |
| rs563880342 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55151440 | AGATAAACTTAGTTT[G/T]CAGAAAACATGGCAG | 166979 |
| rs564000906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55145489 | AGCTGATGATAGGTG[A/G]CAAATTTTGCTTCTG | 166979 |
| rs564049838 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55169887 | GGGAGGCCGAGGCGG[G/T]TGGATCACGAGGTCA | 166979 |
| rs564132177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55131516 | CTTGGACAAAACCCA[A/G]AAGAGTGGGATATCA | 166979 |
| rs564186405 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CDC20B | GRCh38.p7 | 5:55168736 | ACAGAAAATCAATTA[C/T]GGCATGTTCCTCACT | 166979 |
| rs564276411 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55162133 | GGGCGCGGTGGCTCA[C/G]GCCTGTAATCCCAGC | 166979 |
| rs564300732 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55150829 | GGCTCACCGCAGTCT[C/T]GACCTCCCAGAGCTC | 166979 |
| rs564308661 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55151541 | ATTTTTAAAATTCTG[G/T]GTTTAAAAGAGGAAA | 166979 |
| rs564352506 | in-del | -/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55146027 | ATATATACATATACA[-/T]TTCATACAATCTTTA | 166979 |
| rs564372641 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55159403 | TTGTTTAAAAATGCA[A/G]CAGGTGGGGGTGCAT | 166979 |
| rs564431309 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55142199 | TTCTGAAAGTCTCCA[C/T]GGCTATGCAGGCCCT | 166979 |
| rs564476934 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55117556 | GTTTGAAGACCCTGA[C/T]CCAGATCTCAGTCAT | 166979 |
| rs564489727 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55159881 | AGCCCTCCGTAGCTT[G/T]CGAGTTACAAGAGCA | 166979 |
| rs564668879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55137738 | CCTAAGTACAGCAAA[C/T]GACTTTTTTAAGGGG | 166979 |
| rs564679117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55145546 | CCAAATGAGAATTAC[A/G]TATTTCAGAAAGAGA | 166979 |
| rs564690817 | snp | A/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55130596 | AAGATGGAAAATCTA[A/T]CAGAAGTCTGTGCCA | 166979 |
| rs564746983 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55162122 | AAAAAAAGGCCGGGC[A/G]CGGTGGCTCACGCCT | 166979 |
| rs564759610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55136959 | TTGGAAGGCTGAGGC[A/G]GGTGGAGCATCTGAG | 166979 |
| rs564871262 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55139595 | TAAACAATTATACTA[A/G]AAAAGAAGCATAATT | 166979 |
| rs564885440 | snp | A/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55169717 | TCAAGTGAAAAATGT[A/T]TTAGTTGACTGACTC | 166979 |
| rs564958292 | snp | A/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55134966 | ATACTATAATAGTGA[A/T]ACATGTCATTATACA | 166979 |
| rs564959648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55129015 | CCATCATTTCTAACC[A/G]AAAACACCACCCAGC | 166979 |
| rs565080819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55129646 | AATCACCTACATGCA[A/G]AAGAGACTCAAATCA | 166979 |
| rs565115773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55114394 | CTGTAGGCAATGTAA[A/G]TTGGGGCCATGAGTC | 166979 |
| rs565155918 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CDC20B | GRCh38.p7 | 5:55134555 | TTGCCTGAGCCCAGG[A/G]GTTTGAGACCCACCT | 166979 |
| rs565331997 | in-del | -/TA | 0.00478085 | 0.0486577 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55162230 | GTGAAACCCCATCTC[-/TA]TTAATAGTACAAAAA | 166979 |
| rs565333792 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55129127 | TGCTAAGAGAAAACA[G/T]ATTTGTATGACCATT | 166979 |
| rs565334769 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55173970 | AAGATATTGAGGGTT[A/G]AGGAAGAGGTCTGGC | 166979 |
| rs565336802 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164907 | TAACATTTGAAAAAG[C/T]CTTCATCATTTTCAG | 166979 |
| rs565350239 | in-del | -/TA | | | intron-variant | CDC20B | GRCh38.p7 | 5:55135233 | GTGTGTGTGTGTGTC[-/TA]TATATATATATATAT | 166979 |
| rs565384962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55128280 | AAAAAAAAAAAAAAG[C/T]GGAATGTCATCTCCT | 166979 |
| rs565400015 | snp | C/T | 0.00914312 | 0.0669923 | upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55173350 | TGGGCCCCGCCCCGC[C/T]ACCGCCTCCGGCCGA | 166979 |
| rs565453107 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55166348 | GTTTCTTCACTTACA[G/T]CTCTCTAATCTTGGC | 166979 |
| rs565514537 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55159436 | CAGTTCAAAGGAGAA[A/G]TGTTGTTTCTCAGTT | 166979 |
| rs565516621 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CDC20B | GRCh38.p7 | 5:55150879 | AGCTCACCAGTAGCT[C/G]GGACTACAGGTGTGC | 166979 |
| rs565538301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55121859 | TAGCACTTCCCACCA[C/T]GTGGATTTTTTGCCA | 166979 |
| rs565547266 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55158382 | TTACATACATTTTTG[C/T]TCTTTACTAGGAATT | 166979 |
| rs565580369 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55158825 | CCGTTAGCAACAGCA[A/G]AGTTAGGCCCCCTGT | 166979 |
| rs565611408 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55122740 | CTGGCTTGAGGCAAC[A/C]ATGTTGTGAGGAAAC | 166979 |
| rs565721621 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55114147 | CTCATAAAAACCCCA[C/T]GGAGAAGACATAGCC | 166979 |
| rs565776314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55122771 | CCAAATCAGCCCACA[C/T]AACATGAAGATGCTC | 166979 |
| rs565841224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55172851 | TAGAGTTTCGTACCA[C/T]CTCTTGGTCCTAAAC | 166979 |
| rs565925964 | snp | A/C | 0.0337553 | 0.125452 | intron-variant | CDC20B | GRCh38.p7 | 5:55135233 | TGTGTGTGTGTGTGT[A/C]TATATATATATATAT | 166979 |
| rs565931871 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55148557 | TGTCTCTACAAAAAA[C/T]ACAAGAATGAGTTGA | 166979 |
| rs566060557 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CDC20B | GRCh38.p7 | 5:55156745 | CGGGCATTTTGGCGC[A/G]TGCCTGTAGTCCCAG | 166979 |
| rs566089130 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55149516 | ATGCAAGTGATCTAC[A/G]TATCACTCCCAAGAG | 166979 |
| rs566117734 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55165093 | GGTTGCTAATGTATT[C/T]GTACTAGATTAGCCA | 166979 |
| rs566121904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55156223 | AGGGGTAACTACCCC[C/T]ATGATTTAGTTATCT | 166979 |
| rs566131004 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55163353 | ACAGCGAGACCCTGC[C/G]AAAAAAAAAGTTATT | 166979 |
| rs566145709 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55142630 | CATGTTTGAGGCCAC[A/C]AGTGCACCCTAATTA | 166979 |
| rs566345754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55147966 | AGGAGTTTGATATTT[A/G]TAGAGCCTGTAGTAG | 166979 |
| rs566423210 | in-del | -/TT | 0.00119737 | 0.0244387 | intron-variant | CDC20B | GRCh38.p7 | 5:55148341 | GTATCTGGAAAGGAC[-/TT]TTTTGGACAATGTGC | 166979 |
| rs566574425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55132179 | CTTCTTAGTTGGTCA[C/T]GACAATACATTCTCT | 166979 |
| rs566581522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170806 | TGAAACATAGTGGCA[A/G]AACTCTAATCTTAAT | 166979 |
| rs566599241 | snp | C/T | 3.30693e-05 | 0.00406615 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55133455 | AATCTTCACCTCTGG[C/T]TGGAGTATGGAATCG | 166979 |
| rs566638174 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CDC20B | GRCh38.p7 | 5:55169996 | GCAGGCGCCTGTAGT[C/T]CCAGCTACTCCAGAG | 166979 |
| rs566694479 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55125977 | TACACACATAAAAAG[C/T]ATAGCACAGTGCCTG | 166979 |
| rs566710996 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55173536 | ATGTTTCCTTATAAC[A/G]GCCCTGATCCCTGTT | 166979 |
| rs566766646 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55162311 | TGAGGCAGGAGAATC[A/G]CTTGAACCCAGAGGC | 166979 |
| rs566884616 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55140196 | ATTATTCATATTTTA[C/T]AATTAGGTTGATTTA | 166979 |
| rs566957772 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55140583 | TAAACAATATATTAT[A/G]AACAGTGCTGAGCAT | 166979 |
| rs566967372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55118186 | TTAACCCCAAATTTC[C/T]AAACTTACTGACCAC | 166979 |
| rs567016879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55155388 | GAAAAGACCTGCTGG[C/T]GATGCTAGTCTTGCT | 166979 |
| rs567144430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55132579 | CATGAATTCATTTCT[C/T]ATCCCATTTCTTTTC | 166979 |
| rs567339378 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55133155 | ATACATAAGAATAGA[C/T]CATCATTAGTACAAT | 166979 |
| rs567350344 | snp | C/G | 0.000195027 | 0.00987296 | intron-variant, upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55172903 | CGGCCCCGCATTAGA[C/G]AGTTAGGGAGAATGC | 166979 |
| rs567384944 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55173620 | GCGTGCACAGCTCTC[C/T]GGCCTCTGTCCGTTG | 166979 |
| rs567463528 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CDC20B | GRCh38.p7 | 5:55120994 | GAAAAGAGAACTATA[A/T]GTGATTGCTCACAAC | 166979 |
| rs567504319 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55148155 | GACATTAAAAAGACA[A/T]TTCATAAAAGAGATA | 166979 |
| rs567522388 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55114582 | CACCCATTGGGTGGC[G/T]TAAAACAACAGAAAT | 166979 |
| rs567523387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55156840 | GGTTGCACCACTGCA[C/T]TCCAGTCTAGCCGAC | 166979 |
| rs567543932 | snp | A/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55168966 | ACATGTACCCCCTGG[A/T]TCTAAAATAAAATAA | 166979 |
| rs567573644 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55121495 | TTGGGTTGGGTTAAT[A/T]TTTTTTGGAAAGGAG | 166979 |
| rs567590489 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CDC20B | GRCh38.p7 | 5:55148677 | CACTCCAGCCTGGGC[A/G]ACAAAGTGAGACCCT | 166979 |
| rs567677017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, downstream-variant-500B | CDC20B, MIR449A, MIR449B, MIR449C | GRCh38.p7 | 5:55171824 | TGTCCAGGCTGGTCT[C/T]GAAGTCTTGGCCTCA | 166979 |
| rs567692005 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55133036 | TATGGTATCAGTTCC[A/G]TGTCAGTTAGTCCTG | 166979 |
| rs567875950 | in-del | -/C | 0.00636936 | 0.0560724 | upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55173235 | AGTCGGCGCGGGAAT[-/C]CCCCCTCGCCGGCTT | 166979 |
| rs567895807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55163837 | CTTGATACTAAGATC[A/G]CATACTAGATGAGTA | 166979 |
| rs567918128 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55141180 | AGCTCTCATCAACAG[C/G]TTTCTTACACTAGCT | 166979 |
| rs567975548 | snp | C/G | | | intron-variant, downstream-variant-500B | CDC20B | GRCh38.p7 | 5:55136068 | CCTGCCTCAGCCTCC[C/G]GAGTAGCTGGGACTA | 166979 |
| rs568040761 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55153689 | ATTTATTTATCAAAA[C/T]TGTTGATTACTCTAA | 166979 |
| rs568043019 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55132614 | TGGAGGAAAAATAAG[C/G]CTTTACTCTTTGGCA | 166979 |
| rs568109204 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CDC20B | GRCh38.p7 | 5:55153059 | GCCTCGACAATGTGG[C/T]GAAACCCCATCTGAA | 166979 |
| rs568156219 | snp | A/G | 0.000101864 | 0.00713594 | intron-variant | CDC20B | GRCh38.p7 | 5:55140281 | CAGAGAGAGAGGAGC[A/G]CAGGAAAGAAGGACA | 166979 |
| rs568250497 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55139576 | GCAACTTTTAATACT[C/G]AGCTAAACAATTATA | 166979 |
| rs568252221 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CDC20B | GRCh38.p7 | 5:55153218 | CTCTCCAACCTGGGC[A/G]ATATAGCCAGACCTT | 166979 |
| rs568365298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55121301 | GTTTATACTATTTGA[C/T]TATTTTCTGTTGTTT | 166979 |
| rs568368704 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | CDC20B | GRCh38.p7 | 5:55118427 | CAAGGAGTTAAAACT[-/A]AAGTACTTATAGCTT | 166979 |
| rs568390927 | in-del | -/AC | 0.00517822 | 0.0506191 | intron-variant | CDC20B | GRCh38.p7 | 5:55131113 | ACTCCAGCCTGGGTG[-/AC]AGAGTGAAAACCTCC | 166979 |
| rs568489731 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | CDC20B | GRCh38.p7 | 5:55137941 | CAAAATCCCACAAGG[G/T]CTCCGAGGCACAGAG | 166979 |
| rs568590000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55130154 | TCTAAGTAAAGAAAA[C/T]AGAAACCATAAAACA | 166979 |
| rs568666874 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55124140 | ATAAATAATTATGCA[G/T]AACATGGTGGAGCAT | 166979 |
| rs568744430 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55117371 | CACAGCCAAAACTAT[A/T]TTTTATGTAGCAACC | 166979 |
| rs568758748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55169260 | ATCAAATTATAGATA[C/T]CTATTTAACCCATGT | 166979 |
| rs568775497 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55163388 | TTCAAAATAAGGTGA[-/T]TATTCACTTTGGGAG | 166979 |
| rs568808423 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55154327 | GAGTTCCAGACCAGG[A/C]TGGGCAAGTGAGACC | 166979 |
| rs568857870 | snp | A/T | 8.24178e-05 | 0.00641889 | missense | CDC20B | GRCh38.p7 | 5:55146821 | CGCAAAGTTGCTCTT[A/T]AAGTCAGAATACGTA | 166979 |
| rs568944488 | snp | A/G | 5.1656e-05 | 0.00508186 | intron-variant | CDC20B | GRCh38.p7 | 5:55140418 | CATTTCTGAAAATAA[A/G]CACACATAAGGAGAA | 166979 |
| rs569017019 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55140886 | CCCTTCTGACACTCT[C/T]ACATCCAACTTCAAT | 166979 |
| rs569025824 | snp | C/T | | | upstream-variant-2KB | CDC20B | GRCh38.p7 | 5:55174876 | TCCACAGCATACATA[C/T]ACACAGCCTCCAAAT | 166979 |
| rs569127325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, downstream-variant-500B | CDC20B, MIR449A, MIR449B, MIR449C | GRCh38.p7 | 5:55171890 | GATTACAGGCATGAG[C/T]CACAGTGCCTAGTTG | 166979 |
| rs569154707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55139374 | TGAAAAGTCCCAGAA[A/G]ACAACTGTGCAACTG | 166979 |
| rs569243003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55137993 | TAAAAGACTGTCAAG[C/T]TCCCACACATACACA | 166979 |
| rs569285706 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55131722 | GAGAAATAGAAAATT[A/T]TAAGTATAAAGATCT | 166979 |
| rs569302450 | snp | C/T | | | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55163631 | ACTGTCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 166979 |
| rs569303308 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55123581 | ACTGTTCAGTGATTC[A/C]CCAGGTGCTGACTGC | 166979 |
| rs569342236 | snp | C/T | | | intron-variant, utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55136952 | CAGTATTTTGGAAGG[C/T]TGAGGCGGGTGGAGC | 166979 |
| rs569407666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55162238 | CCATCTCTATTAATA[A/G]TACAAAAATTAGCCA | 166979 |
| rs569416160 | snp | A/C/T | 0.00159649 | 0.0282165 | intron-variant | CDC20B | GRCh38.p7 | 5:55116393 | GCAACATAGAAAGAT[A/C/T]CAGCCTCCTAAAAAG | 166979 |
| rs569438357 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55129360 | ACTAAGTAAGGGAGT[C/T]AAAATTTGGAGAAGC | 166979 |
| rs569500416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55145170 | TCCCTCAATTGCAAT[A/G]AGATACAAAAGATTT | 166979 |
| rs569501794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55124748 | TTTTTATATGTGAAG[A/G]ATACCCAGTGGCCTC | 166979 |
| rs569540327 | snp | C/G | | | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55159232 | TTCTTGCCCAAGTTG[C/G]TCTTGAACTCATGGG | 166979 |
| rs569562029 | snp | G/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55140131 | AAAGGTGGTCACCTA[G/T]AGAGAATGGGACTTG | 166979 |
| rs569577342 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CDC20B | GRCh38.p7 | 5:55118812 | CCAGTCGGGCTCATC[A/G]TCAGAGGCAGGAAGT | 166979 |
| rs569581021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55129985 | ACCAATAGATGAAAA[C/T]TCCAAGGTGACCTAG | 166979 |
| rs569753016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55168104 | ATCTTTCCCATCAAA[C/T]AAAATTCTAATAATT | 166979 |
| rs569800990 | snp | C/T | 0.000399281 | 0.0141238 | missense, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160274 | CTGTCTATAGTTCTA[C/T]GCACAGTAACGCTAT | 166979 |
| rs569975011 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55151197 | AGCAAGAACACATTG[A/G]GACACATCGTCTCAT | 166979 |
| rs570078312 | snp | A/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55121893 | AAGCACCTACATCTT[A/T]ACGCTTTTCTTACAA | 166979 |
| rs570103420 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55117295 | GGTTAACAGGGTACG[G/T]CTTAGTAAAGGTGTG | 166979 |
| rs570226032 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55136523 | AAGATCACACTACTG[C/T]ACTCCAGCCTGGACG | 166979 |
| rs570270313 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55144049 | TGGATAGAAACAGTT[A/C]CATAGTTTTAAATGA | 166979 |
| rs570301466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55138362 | GATGGGGTCTCACCA[C/T]GTTGGCCAGGCTGGT | 166979 |
| rs570439569 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55139459 | AAGAAACTGGAGTGA[C/G]TGAGTGCATGGAAAA | 166979 |
| rs570498900 | in-del | -/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55141252 | CCCACACACACAGCT[-/G]CAAGACTGGCTCTCC | 166979 |
| rs570505796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55169065 | TAGTAGGTTTTATTT[C/T]TATCACTAGGTCAGT | 166979 |
| rs570629109 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55145803 | CTCCCCCCATCCATC[C/T]CCTCATCCCTCTCTC | 166979 |
| rs570648215 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55149815 | CATTGGAAATACACT[A/G]AAGACCACTGAATTG | 166979 |
| rs570680886 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55152921 | GCAAGGAAATAAGCT[A/G]TTTTCATCCTTCTCC | 166979 |
| rs570761675 | in-del | -/TC | 0.00119737 | 0.0244387 | intron-variant | CDC20B | GRCh38.p7 | 5:55145775 | CCTCTCTTCTCTCTT[-/TC]TCTTTGTCTCTCTCC | 166979 |
| rs570785684 | snp | C/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55118945 | GCATGTCTCCTCTCA[C/G]AAAAGTGTAGGCTCC | 166979 |
| rs570828108 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55150802 | TAGGCTGGAGTGCAG[C/T]GGCACAATCATGGCT | 166979 |
| rs570895515 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55115385 | TACTAGAAGCATTAC[A/G]AATGTTTCGGAGATG | 166979 |
| rs570908594 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | CDC20B | GRCh38.p7 | 5:55135688 | AGGGCACATGCAGCC[C/G]AGGAGGGCTTTGAAT | 166979 |
| rs570932499 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55144788 | AAGAGGTCAGGTCCA[A/T]CAGCCTAAGAAAGAA | 166979 |
| rs570994963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55129383 | GGAGAAGCAAACTGG[C/T]GGGGGGTAAGTTTCC | 166979 |
| rs571025232 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55173633 | TCCGGCCTCTGTCCG[C/T]TGGTAATCGCTGTGT | 166979 |
| rs571137288 | snp | A/C/G | 0.00199481 | 0.0315187 | intron-variant | CDC20B | GRCh38.p7 | 5:55123639 | GGAGACTCTCTCTTA[A/C/G]TGAAAAGGACTCCCA | 166979 |
| rs571149771 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55166254 | TGCACTGGGAACAAC[C/G]AGGACTGTCCCAGTC | 166979 |
| rs571166666 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55135092 | TTGTAACAAATGTAC[C/T]ACTCTGGTGGGAGAT | 166979 |
| rs571289801 | in-del | -/TTTTTTT | 0.427727 | 0.175821 | intron-variant, upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55172750 | CTTGTCAGATTACAC[-/TTTTTTT]TTTTTTTTTTTTTTT | 166979 |
| rs571300494 | snp | C/T | 0.00159617 | 0.0282053 | downstream-variant-500B | CDC20B | GRCh38.p7 | 5:55112638 | GAATTACTAACATTA[C/T]CAAACAGATCTAAAT | 166979 |
| rs571317067 | in-del | -/CTCAATAT | 0.00953873 | 0.0683987 | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164565 | CAGTGACCAATGTGC[-/CTCAATAT]CTTATTGTTCAACTT | 166979 |
| rs571337142 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CDC20B | GRCh38.p7 | 5:55119565 | TCACCACTCCATCAT[C/T]CATATACATATGCAA | 166979 |
| rs571484535 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55158791 | ATTGCCTCCCCATAC[C/T]TACCCCTAAAATTCA | 166979 |
| rs571555974 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55148755 | CCAAGATGGAGAAAA[C/G]ATCCAGCATTTATTG | 166979 |
| rs571611011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55156148 | AGCTTGTGCTGAAGA[A/G]CTCCCATTTATAAAA | 166979 |
| rs571743480 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55165583 | CAAAGTTATTAGATA[A/C]ACCAAAAATATTTCA | 166979 |
| rs571797156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55149273 | ATTGCAAGTGTACAG[A/G]ATGTGAAAGGATGCA | 166979 |
| rs571853624 | snp | A/G | | | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55163074 | AATTTGAAGCACGGA[A/G]CGTACATTAATCTGG | 166979 |
| rs571858171 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CDC20B | GRCh38.p7 | 5:55156737 | AAATTAGCCGGGCAT[G/T]TTGGCGCGTGCCTGT | 166979 |
| rs571944776 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55166341 | AAAGTGGGTTTCTTC[A/G]CTTACATCTCTCTAA | 166979 |
| rs572040136 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | CDC20B | GRCh38.p7 | 5:55121240 | CCCTCATTTTTGCAT[A/C]CTCTCTTCTACACAT | 166979 |
| rs572046633 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CDC20B | GRCh38.p7 | 5:55149755 | GAGTTTTCTTTTGAG[A/G]TGATGAAAACATTTT | 166979 |
| rs572176702 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55126076 | TAATGAAACTAAATT[C/T]TAACAATGCAGATTA | 166979 |
| rs572186415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55143773 | TCGTCACTCCAAAGT[C/T]CATTGCAGAGAGCAG | 166979 |
| rs572189181 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CDC20B | GRCh38.p7 | 5:55143104 | TTAAAAGACCATCAT[A/G]TAGAGCAATAATTCA | 166979 |
| rs572246886 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55150245 | ATAGTGAATAAAACA[C/T]GCAAATGCTTACAAT | 166979 |
| rs572365529 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55148654 | AGTGAGCCGCATTGG[A/C]GCTGCTGCACTCCAG | 166979 |
| rs572390297 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55148415 | AATATCACCTCTAAG[A/T]ATTTAAAAAAGAAAT | 166979 |
| rs572402446 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164555 | TCAGAATACACAGTG[A/G]CCAATGTGCCTCAAT | 166979 |
| rs572483664 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55171192 | GGTGGTGCTGCCTGT[-/A]ATCCCAGCTACTCAG | 166979 |
| rs572616136 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55156942 | TTTACTGCCTTGTAA[C/T]CCTTCCGTTTCTTGT | 166979 |
| rs572658267 | snp | C/G/T | | | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55158767 | GGCTTTTAGGATATA[C/G/T]AGCCCTCAATTGCCT | 166979 |
| rs572659883 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55173112 | AAACCCCTGGAGTCC[C/T]GTCCCCCAGGACCAT | 166979 |
| rs572813863 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | CDC20B | GRCh38.p7 | 5:55112711 | ACTAATTTAACAGAA[A/G]AGTCCTAAACTCCCC | 166979 |
| rs572866660 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55132784 | TCCCCAATGTATCTT[C/T]TTCATTGCCATTAAA | 166979 |
| rs572946699 | snp | A/G | | | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55163839 | TGATACTAAGATCAC[A/G]TACTAGATGAGTAGA | 166979 |
| rs572989701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55119151 | ACAAGAGATTGGATG[C/T]CGGTGCCCTGTTCTT | 166979 |
| rs572991406 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55119645 | AAACATTCAACTATA[C/T]GCTCTCTGAGGTAGG | 166979 |
| rs573057882 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55144289 | CAATGTTACTTGCAT[C/T]AATATTATTCCTATC | 166979 |
| rs573102584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55162845 | CAAAAAGGTAACAGT[A/G]AGTTAAGGTGTCATT | 166979 |
| rs573122464 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55142208 | TCTCCACGGCTATGC[A/C]GGCCCTCGTTGTGGA | 166979 |
| rs573128514 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55155734 | GCAGGGTCTACAGAG[A/C]ATCTTTAGCACCCAC | 166979 |
| rs573189665 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55163309 | AGGATCACTTTAGTG[C/G]CCAGGAGTTCAAGCC | 166979 |
| rs573290870 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55132874 | TCTCCTCTATACCTT[C/T]CCAAGTTCTAATGAT | 166979 |
| rs573327581 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55153686 | GAGATTTATTTATCA[A/C]AATTGTTGATTACTC | 166979 |
| rs573337348 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CDC20B | GRCh38.p7 | 5:55146314 | CTTCCAATTCCTATC[C/T]ATAAATGCTGCCCGC | 166979 |
| rs573426493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55146012 | GTATGTGTACATATA[C/T]ATATATACATATACA | 166979 |
| rs573431715 | in-del | -/TC | | | intron-variant | CDC20B | GRCh38.p7 | 5:55115610 | AGGGAGGAAAGGAGG[-/TC]AGATATGGTTTTGAG | 166979 |
| rs573588946 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55133672 | AAACTACAGTACAAA[C/G]AGCCGGGGAAGGAAG | 166979 |
| rs573635824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55119231 | GATACTCTACTCACC[C/T]TTGAGCCCCCTTTAA | 166979 |
| rs573661006 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, downstream-variant-500B | CDC20B, MIR449A, MIR449B, MIR449C | GRCh38.p7 | 5:55172102 | TTGTTTCCTTTTACA[A/C]TGATTACAGGAGACA | 166979 |
| rs573798187 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CDC20B | GRCh38.p7 | 5:55119674 | GGGTGGATGTAGGAC[C/T]TTTTCCTCTGATGAA | 166979 |
| rs573939010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55149097 | CTAACAGGACATCTC[C/T]AAGAGGGACTGCTCT | 166979 |
| rs573986486 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55161976 | CATTTGTAAAATGGG[C/T]TATCAATAGTACCGC | 166979 |
| rs574002418 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55156308 | GGGTGGGGACACAGC[A/C]AAACCATATGACCCC | 166979 |
| rs574176707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55130460 | GGTGACCATGGGGTT[C/T]TCACCAGATACCATG | 166979 |
| rs574219340 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CDC20B | GRCh38.p7 | 5:55154450 | TGATCCTGGGAGGTC[A/G]ACGCTGCAGTGAGCC | 166979 |
| rs574221030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55139811 | AGGAGGGTCACTTGC[A/G]GCCAGGAGTTCGAGA | 166979 |
| rs574250787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55124489 | CCAAATGACATTACT[C/T]AAAGCCTTAGATCCA | 166979 |
| rs574356851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, stop-gained | CDC20B | GRCh38.p7 | 5:55137610 | CCTCCTGTTCAAATC[A/G]TTTCTTCATGCTGCC | 166979 |
| rs574394592 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55145543 | TGCCCAAATGAGAAT[C/T]ACATATTTCAGAAAG | 166979 |
| rs574410556 | snp | C/T | 1.64784e-05 | 0.00287035 | missense | CDC20B | GRCh38.p7 | 5:55124969 | TTGTGGCGAAGTGTT[C/T]CAACATGATGCTGGG | 166979 |
| rs574419094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55138683 | TAAAATAATATTGTC[A/G]GAGATATAGGAGAAG | 166979 |
| rs574419777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55145467 | AAGAAAGAATGGGAA[C/T]TACATCAGCTGATGA | 166979 |
| rs574442232 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55116926 | TTTCTCTCACATCAG[C/T]GACAATCTTAATTTA | 166979 |
| rs574608749 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55134145 | GTTCTCATCAAAAGA[C/T]CATACTAAGTTCAAA | 166979 |
| rs574696598 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55117650 | ATAAAAATTAAATAC[C/G]TAGGCCAGGGGACAC | 166979 |
| rs574700051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55122356 | GTCAATGAAGCCTCA[A/G]TCTCCCTGGGGCTCA | 166979 |
| rs574716124 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC20B | GRCh38.p7 | 5:55175037 | ATATTACAGTAATAA[C/G]TGTCAAGAATACTAA | 166979 |
| rs574968022 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CDC20B | GRCh38.p7 | 5:55168534 | CATCTCTTTAACATA[A/T]TTTTTATTTCTTTAA | 166979 |
| rs575163218 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55131407 | AAGATGTCCAAGGAA[C/G]AGGCCTTGGGTACTC | 166979 |
| rs575184535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55119028 | AAAAAGTACCTCCCA[C/T]ATAATAGATGCTTCA | 166979 |
| rs575231769 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55151376 | CCACTATGTCCAGGT[A/T]GCCCTTACCCTCACA | 166979 |
| rs575233704 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55159674 | TCAGATATTTCCCTG[C/T]TCTTTCCACTATAAA | 166979 |
| rs575250129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55138953 | AAAAATAAATGACAA[C/T]AAAAAAAATATTAAA | 166979 |
| rs575326067 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55138432 | CCCAAAATGCTAAGA[C/T]TGCAGGCTTGACCCA | 166979 |
| rs575349294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55125533 | TTGCTAAAGAACTAA[A/G]CTTCTTTGTAAAAGA | 166979 |
| rs575375018 | in-del | -/T | | | intron-variant, upstream-variant-2KB | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55171607 | CACTTGAATACTGAA[-/T]TTTTTTTTTTTAAGA | 166979 |
| rs575463349 | snp | C/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55141546 | TTATACGCCTGTGCT[C/G]TATACTCACTGAGTC | 166979 |
| rs575538755 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CDC20B, MIR449A | GRCh38.p7 | 5:55170142 | AAAGAAACTAATAAT[A/G/T]CAGAAAGAATCCTAA | 166979 |
| rs575663564 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55123831 | GGGAATTTGGACCGA[A/T]CATCATTCTCAATAT | 166979 |
| rs575693449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55151084 | TTTTTATTTCTCTCC[A/G]CTAAGAAAAAAACCG | 166979 |
| rs575748638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55123187 | AATGTAATGTTTTCA[A/G]TCAAAATAAAATATC | 166979 |
| rs575782013 | snp | C/T | 1.72136e-05 | 0.00293369 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160981 | CGGTTGGATTTTTTT[C/T]TTTTTCCGGGAGGTT | 166979 |
| rs575798478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55133013 | ATTATTTATAATCTA[C/T]CTTGGCATATGGTAT | 166979 |
| rs575944884 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55152277 | TGTCTAAGCTACAAA[C/G]TTTCTGGTAATTTGT | 166979 |
| rs575969406 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CDC20B | GRCh38.p7 | 5:55145964 | GTCATTAAAATTCTA[C/T]ACTTTGCAAAACAAA | 166979 |
| rs576016915 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55114924 | GGTTCCAGAGATTTA[G/T]CATGGGTATCCTTTA | 166979 |
| rs576023423 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55158208 | AAATGCCCAGGTGAT[G/T]GTACTGTGGAAGGTC | 166979 |
| rs576049838 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55130670 | TAAAGGGACAATATA[C/T]GAAAGAGAAACTTGG | 166979 |
| rs576106469 | snp | A/C | 1.64863e-05 | 0.00287104 | missense | CDC20B | GRCh38.p7 | 5:55127288 | GATTCCAGCTCAGAG[A/C]CCCAACTACTGACAA | 166979 |
| rs576156939 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55150121 | TGGGCAACAAGAGTG[A/G]AACCCCGTCTCAAAA | 166979 |
| rs576182607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55121284 | AAAGTAGCAAACATC[A/G]TGTTTATACTATTTG | 166979 |
| rs576205921 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CDC20B | GRCh38.p7 | 5:55136287 | GGGACACGGCAGGTG[C/G]AGTGGTTCACACCTG | 166979 |
| rs576342128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55134514 | ATGCCTGTAATCTCA[A/G]CACTTTAGGAGCTGA | 166979 |
| rs576369378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55142758 | TGCATATGAGTTCAG[A/G]TAACTAAAATTTATA | 166979 |
| rs576404842 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55142136 | TCCTAGATGAGATCG[A/T]CTTACTACTTTAATC | 166979 |
| rs576406646 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55144512 | ATTCTCACTAATGTT[A/C]CTAGAGCCTAGTACC | 166979 |
| rs576452513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55135270 | AGAGAAAGAGAGAGG[A/G]AGAGAGAGAGACTCC | 166979 |
| rs576495775 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55136967 | CTGAGGCGGGTGGAG[C/T]ATCTGAGGTCAGGAG | 166979 |
| rs576630556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55137551 | CAACAGAGCCTTGCA[C/T]AGAGTATTCAGAGGG | 166979 |
| rs576661531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55157195 | TTTTCTAACATACTA[C/T]CCCTTATGCAGAGAA | 166979 |
| rs576668663 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55166428 | TGCCCTTTAGGTAAG[C/T]AGAGTAGGCAGGAGG | 166979 |
| rs576740927 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55152041 | CAGAGGGAGATGTGA[C/G]TGCACACAGAAAAGG | 166979 |
| rs576811518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55151194 | CACAGCAAGAACACA[C/T]TGAGACACATCGTCT | 166979 |
| rs576828885 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55137856 | ATAACTGACCAAGAA[A/G]AGCATAAGAAACTAC | 166979 |
| rs576978696 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55145218 | TAACAATGTTTTTCA[A/C]AACCCTTTATCTCCT | 166979 |
| rs577009122 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55150105 | CCATTGCACTCCAGC[C/T]TGGGCAACAAGAGTG | 166979 |
| rs577090113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55123887 | CAGGAATATTGGGCC[A/G]GTACAATGTAGTGGC | 166979 |
| rs577113808 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55113569 | ACAGGATGTGACTAG[A/G]TGAAGCAAAAGAAAA | 166979 |
| rs577126732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55128281 | AAAAAAAAAAAAAGC[A/G]GAATGTCATCTCCTT | 166979 |
| rs577273036 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55165545 | TGCTACCTCAGTATA[G/T]AGTTCTGTATACGTA | 166979 |
| rs577336301 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164411 | GAAGGATTTTTTTTT[A/T]ATGTTATCTTGCTAT | 166979 |
| rs577403854 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55122208 | AATTAAATCACCTAC[G/T]TTATTTGGACTAAAG | 166979 |
| rs577405416 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CDC20B | GRCh38.p7 | 5:55174901 | CCAAATGTCTTTTTT[C/T]CCCCTAGTGTGAAGT | 166979 |
| rs577485835 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55158383 | TACATACATTTTTGT[C/T]CTTTACTAGGAATTA | 166979 |
| rs577538828 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55166488 | TTGAAAGAAAGGACA[C/T]TCAGGTGTCCCTTCG | 166979 |
| rs577591143 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CDC20B | GRCh38.p7 | 5:55147464 | AAAGTTATATTTTAT[G/T]TTTATATTTATAAAA | 166979 |
| rs577604904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55126986 | ACTTAGCACAGAGAA[A/G]CCTTTTGCTTGAAGG | 166979 |
| rs577618266 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | CDC20B | GRCh38.p7 | 5:55156576 | GCAGTATAAAGCTCT[C/T]TAAAAACATAAGTCA | 166979 |
| rs577629933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | GPX8, CDC20B | GRCh38.p7 | 5:55167459 | AGACTCTGGAGGAGG[A/G]ATCCTGACATACAGC | 166979 |
| rs577675901 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CDC20B | GRCh38.p7 | 5:55148277 | ACAATCCCTGGTGTT[A/G]AAGGTGCCAAAAACA | 166979 |
| rs577679663 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55140686 | TCTTTTTTTACTCTT[A/C]TAGCCTAAAAATCTG | 166979 |
| rs577865002 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55141211 | CTCTACACTGTTCAC[A/C]TTTATCTTGGCTGCT | 166979 |
| rs577910140 | snp | A/G | 0.000292783 | 0.0120957 | intron-variant, upstream-variant-2KB, nc-transcript-variant | CDC20B, MIR449A, MIR449B, MIR449C | GRCh38.p7 | 5:55172282 | TGAATGCAACAGAGA[A/G]GAGTGCAACTAGCAA | 166979 |
| rs577990087 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CDC20B | GRCh38.p7 | 5:55154742 | ATATGGTTCATAGTG[G/T]TATAGATGAACACTA | 166979 |
| rs578100766 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55133792 | CCTGAATGTAGAAGA[C/T]AGATCTTGTGAGGAG | 166979 |
| rs578115442 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55157943 | ATTAATTTTAAAATG[A/C]ATGTTCCTAAGCCAT | 166979 |
| rs578169493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CDC20B | GRCh38.p7 | 5:55126228 | TGGGATGGCCAGGCG[C/T]GGTGGCTCACACCTG | 166979 |
| rs578175738 | in-del | -/AAGA | 0.000861384 | 0.0207352 | intron-variant | CDC20B | GRCh38.p7 | 5:55143648 | TTTGCGGGATCCTAC[-/AAGA]AAGACATTTATCTTT | 166979 |
| rs578208402 | snp | A/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55130557 | ACCCAGAATTCTATA[A/T]CCAGCAAAAATCTCA | 166979 |
| rs745338696 | snp | A/C | 1.65258e-05 | 0.00287448 | missense | CDC20B | GRCh38.p7 | 5:55133485 | GTTTATATCACCAGA[A/C]CTTTTAAGATGGAAG | 166979 |
| rs745362547 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55142103 | GCGCTTCTGTTCTGT[A/G]GGTGCAGGGGTGCTC | 166979 |
| rs745362738 | snp | C/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55156571 | TGTGTGCAGTATAAA[C/G]CTCTCTAAAAACATA | 166979 |
| rs745413844 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55155639 | ACGCCCTCCCATCCT[A/G]GTAGGCAATATGACC | 166979 |
| rs745455109 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55133905 | ACCAAGACTTACCTG[A/G]TACACCTATGCCCTA | 166979 |
| rs745455525 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55118027 | GGGAGGCTGAGGCAG[A/G]AGAATTGCTTGAACT | 166979 |
| rs745490398 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55168074 | CTATCCATATTTAGT[A/C]CTCTGCTTGATTTTA | 166979 |
| rs745520180 | snp | C/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55167016 | ACCTGGGCAACAGAG[C/T]GAGACCCCATCTTAA | 166979 |
| rs745520452 | snp | C/T | 1.64765e-05 | 0.00287019 | intron-variant, missense | CDC20B | GRCh38.p7 | 5:55120528 | GCAAGGACCCCAGAC[C/T]GCCAGGGACACCAAT | 166979 |
| rs745577503 | snp | C/T | 1.65466e-05 | 0.00287628 | intron-variant, upstream-variant-2KB, downstream-variant-500B | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170636 | AGGTATCCAGAGCAC[C/T]TCATTGACAAGAAGA | 166979 |
| rs745691223 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55155625 | TGTTTGAACTTTCAA[A/C]GCCCTCCCATCCTAG | 166979 |
| rs745699014 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55127872 | GACTTCACAGCATTC[A/C]TTATCATTGCAGAGA | 166979 |
| rs745720067 | snp | C/T | | | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55163526 | TTTAATTTTATTTGA[C/T]ACAGAGTTTCACTCT | 166979 |
| rs745723019 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55120407 | AAAATGAAGATGAAG[C/T]CCAGAGGAGATATTA | 166979 |
| rs745726830 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55126133 | CTGCAATAACTAAGT[C/T]GTTTTAAGACCGGCC | 166979 |
| rs745779383 | snp | C/T | 1.80403e-05 | 0.0030033 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160957 | TTTAAAATCTTTTGC[C/T]TCACTTTCCGGTTGG | 166979 |
| rs745793015 | snp | A/T | 1.73243e-05 | 0.0029431 | intron-variant | CDC20B | GRCh38.p7 | 5:55133380 | CATTTTGTCATTTCA[A/T]CTTTTAATTCCCAAT | 166979 |
| rs745865796 | snp | C/T | 1.75256e-05 | 0.00296015 | intron-variant | CDC20B | GRCh38.p7 | 5:55140423 | CTGAAAATAAACACA[C/T]ATAAGGAGAATATTT | 166979 |
| rs745890922 | snp | A/C | 1.79293e-05 | 0.00299405 | intron-variant, downstream-variant-500B | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170493 | AAAGTACACATAAAC[A/C]CACACTAATTACAGA | 166979 |
| rs745938479 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55121487 | GATTTGTATTGGGTT[A/G]GGTTAATTTTTTTTG | 166979 |
| rs746018437 | snp | C/T | | | missense | CDC20B | GRCh38.p7 | 5:55114241 | AATTCCATACAGAGG[C/T]CGTCCCATCAGCTGC | 166979 |
| rs746029860 | snp | A/G | | | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55163003 | TCTCATCTGCAAAAC[A/G]GGGATGATAATAATA | 166979 |
| rs746039332 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55151356 | GGGCTACATTTGCAA[C/T]GGCTCCACTATGTCC | 166979 |
| rs746056921 | snp | A/T | 1.6483e-05 | 0.00287076 | missense | CDC20B | GRCh38.p7 | 5:55124974 | GCGAAGTGTTCCAAC[A/T]TGATGCTGGGCTACC | 166979 |
| rs746091459 | snp | A/C | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164569 | GACCAATGTGCCTCA[A/C]TATCTTATTGTTCAA | 166979 |
| rs746154788 | snp | C/T | 1.65108e-05 | 0.00287317 | missense | CDC20B | GRCh38.p7 | 5:55143557 | AGTCTCTGTCCATTG[C/T]ATGAGGTGCCTTGCA | 166979 |
| rs746199551 | snp | C/G | 1.91922e-05 | 0.0030977 | intron-variant | CDC20B | GRCh38.p7 | 5:55128387 | GTAATAATACACAGA[C/G]AACATGATGAGAAAA | 166979 |
| rs746220389 | snp | C/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55146623 | TGGCGTTTGGGGCAC[C/G]TCACCTAGAGTCAAG | 166979 |
| rs746251568 | in-del | -/C | 5.0497e-05 | 0.00502453 | intron-variant | CDC20B | GRCh38.p7 | 5:55143508 | GTTTTTTTCTCTTTA[-/C]CTACCTGCCCTTTTG | 166979 |
| rs746319341 | snp | C/T | | | upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55174195 | ATGTGAGTTTGTGTG[C/T]TTTTCTGGGGAAACA | 166979 |
| rs746321481 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55122967 | TAATGAAATGATTAT[C/T]GTTTTAAGCCACTAA | 166979 |
| rs746326540 | in-del | -/TTTTTTT | | | intron-variant, upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55172751 | TTGTCAGATTACACT[-/TTTTTTT]TTTTTTTTTTTTTTT | 166979 |
| rs746353980 | snp | C/T | 1.64909e-05 | 0.00287144 | missense, splice-donor-variant | CDC20B | GRCh38.p7 | 5:55119812 | TTACCAAAAAACCCA[C/T]CTGACCTGGACACAG | 166979 |
| rs746397593 | snp | C/T | 1.65674e-05 | 0.00287809 | intron-variant | CDC20B | GRCh38.p7 | 5:55114349 | AAGACAGTTCATACT[C/T]CTCCACGTTACATGG | 166979 |
| rs746422021 | in-del | -/AA | | | intron-variant, utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55137177 | GCGAGACTCTGTCTC[-/AA]AAAAAAAAAAAAAAA | 166979 |
| rs746436601 | in-del | -/TC | 1.80046e-05 | 0.00300033 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160440 | TATCATTTTTCCTTG[-/TC]TCTGTTTATTCCTCT | 166979 |
| rs746464256 | snp | C/T | 1.64852e-05 | 0.00287094 | missense, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160266 | CAGTTTTGCTGTCTA[C/T]AGTTCTATGCACAGT | 166979 |
| rs746470435 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55117913 | TAAGGTCAGGAGTTC[A/G]AGCCCAGCCTGGCCA | 166979 |
| rs746487858 | snp | A/C | | | missense | CDC20B | GRCh38.p7 | 5:55128513 | AAGTGAGACTTAAGT[A/C]TATGTTTTCAATCCC | 166979 |
| rs746520532 | snp | C/T | | | synonymous-codon | CDC20B | GRCh38.p7 | 5:55119877 | AGTACCTTGACCAGT[C/T]GCAATCTCCTTTGTC | 166979 |
| rs746535735 | in-del | -/T | 3.33976e-05 | 0.00408628 | intron-variant | CDC20B | GRCh38.p7 | 5:55119965 | GCAATTTCTGATTCC[-/T]TATGAATATAGTTAA | 166979 |
| rs746547676 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55132428 | TCAAATAATCTGCCA[A/G]ACTGCTTCTATGTCT | 166979 |
| rs746598453 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55131316 | AATCCCTAGAAAAAT[A/G]ACGACAAAACACAAT | 166979 |
| rs746655038 | snp | C/T | 3.29663e-05 | 0.00405981 | intron-variant | CDC20B | GRCh38.p7 | 5:55120390 | CAAGATTCCAGAAGA[C/T]CAAAATGAAGATGAA | 166979 |
| rs746658454 | snp | C/T | 5.4736e-05 | 0.00523116 | intron-variant | CDC20B | GRCh38.p7 | 5:55128661 | AATTATACAGCCACA[C/T]GAAAACATGTTCAAA | 166979 |
| rs746720568 | in-del | -/AA | 0.00026651 | 0.0115405 | intron-variant | CDC20B | GRCh38.p7 | 5:55128399 | AGAGAACATGATGAG[-/AA]AAAAAAAAACTGGCC | 166979 |
| rs746734221 | snp | G/T | 4.94262e-05 | 0.00497098 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55124917 | GCTGGAAAGCAGCCT[G/T]CCATCCGGTGACCAC | 166979 |
| rs746754909 | snp | G/T | 1.65195e-05 | 0.00287393 | missense | CDC20B | GRCh38.p7 | 5:55143543 | AACACTTTCTTTCCA[G/T]TCTCTGTCCATTGCA | 166979 |
| rs746799433 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55148781 | TATTGAGTAGTTACT[A/G]TGTATGAAACCATAT | 166979 |
| rs746904316 | snp | C/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55155430 | AGAAAGATAAAAGTA[C/G]CAAAGACAGCCCAGG | 166979 |
| rs746978641 | snp | G/T | 1.64781e-05 | 0.00287033 | missense | CDC20B | GRCh38.p7 | 5:55124966 | TGCTTGTGGCGAAGT[G/T]TTCCAACATGATGCT | 166979 |
| rs747022560 | snp | A/T | 1.65545e-05 | 0.00287697 | stop-gained, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55161210 | ATCTTCCACAAGATT[A/T]AGATTCTAGGATCTG | 166979 |
| rs747070025 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55134170 | TTCAAACCACAGGCC[A/G]CTGTCTTTTCATCTC | 166979 |
| rs747125001 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55149951 | CCAGCCTGACCAATA[C/T]GATGAAACCCCATCT | 166979 |
| rs747159317 | snp | A/G | | | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55163233 | ATTTATCAAAAGGAT[A/G]TCATGGCTGGGCATG | 166979 |
| rs747296757 | snp | C/T | 1.64898e-05 | 0.00287135 | synonymous-codon, intron-variant, utr-variant-3-prime, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164128 | TCAAGTTGTGAAGTT[C/T]TGGAAGCCAGAGGAG | 166979 |
| rs747315510 | in-del | -/AA | | | frameshift-variant, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55161069 | CTGAAGGAACTGCAC[-/AA]AGAGTTTGGACCATC | 166979 |
| rs747358055 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55115303 | GTTTAATGTTCACAC[C/T]AATTTGGAAGCTTTG | 166979 |
| rs747433961 | snp | C/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55156814 | AAGAGATGGAGGTTG[C/G]AGTGAGCCGAGGTTG | 166979 |
| rs747434085 | snp | A/G | | | intron-variant, upstream-variant-2KB, downstream-variant-500B | CDC20B, MIR449A, MIR449B, MIR449C | GRCh38.p7 | 5:55172085 | TATAAAACCATTTAA[A/G]TTTGTTTCCTTTTAC | 166979 |
| rs747438813 | snp | G/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55145163 | AAAACTGTCCCTCAA[G/T]TGCAATGAGATACAA | 166979 |
| rs747455036 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55135890 | TCTGTATTTAGAAGT[C/T]AAAAGTGTGTATCTA | 166979 |
| rs747481659 | snp | A/C | 1.66313e-05 | 0.00288364 | intron-variant | CDC20B | GRCh38.p7 | 5:55127402 | GAGTTTTCACAGCCC[A/C]CTGTCTTCTCAAAGG | 166979 |
| rs747510518 | snp | C/G | 1.65228e-05 | 0.00287422 | missense | CDC20B | GRCh38.p7 | 5:55114261 | CCATCAGCTGCAGCA[C/G]AAAACACCCGGGTCT | 166979 |
| rs747525109 | snp | C/T | 4.94214e-05 | 0.00497074 | stop-gained | CDC20B | GRCh38.p7 | 5:55146752 | AGTTTGACTTTGCTG[C/T]CACCTTGTGGTAATG | 166979 |
| rs747570303 | snp | A/T | 3.2969e-05 | 0.00405998 | intron-variant, upstream-variant-2KB | CDC20B, MIR449B, MIR449C | GRCh38.p7 | 5:55172674 | ACACAGATAACATAT[A/T]GAGGGAGAAACTATT | 166979 |
| rs747597329 | in-del | -/T | 1.75154e-05 | 0.00295929 | intron-variant | CDC20B | GRCh38.p7 | 5:55133578 | ATCCTGAAAATATAA[-/T]ATTTATTCTTGTGGG | 166979 |
| rs747608969 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55131156 | CCTCAAAAAACAATA[A/G]CAAACAAACAAACAC | 166979 |
| rs747636803 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55124454 | AGAGATAAGCAGAGC[C/T]AAGAGCTAAAAAGAT | 166979 |
| rs747654292 | snp | C/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55114857 | ATGATTTTATTTCCA[C/G]ATCCTTAATGACATC | 166979 |
| rs747661997 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55146422 | CTAAAGTTTTGTTTT[C/T]GTTTTTGTTTTTAAA | 166979 |
| rs747684704 | in-del | -/TGAAG | 6.59457e-05 | 0.00574182 | frameshift-variant, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160342 | CAGCTTTTATGCCTT[-/TGAAG]TGAAGGATGCAAAAG | 166979 |
| rs747689487 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55122012 | TTCTCCACTCCTTCT[A/G]TAAAACATACTTACT | 166979 |
| rs747715607 | snp | C/T | 1.64732e-05 | 0.0028699 | intron-variant, upstream-variant-2KB | CDC20B, MIR449A, MIR449B, MIR449C | GRCh38.p7 | 5:55172585 | AACAAGCCCTGGACT[C/T]ACGTTGGCGGAATCT | 166979 |
| rs747740758 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55148314 | GGCATACACTGCTGT[A/G]GAGGTTAAATTAGTA | 166979 |
| rs747774198 | snp | A/G | 1.64846e-05 | 0.0028709 | missense | CDC20B | GRCh38.p7 | 5:55128485 | ATCCAGGACACAGAA[A/G]AGATATAGTTACAAG | 166979 |
| rs747795595 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55145654 | CTCTGCCCCAACATA[A/G]GCATCAGACTGTCTC | 166979 |
| rs747859674 | snp | A/T | 1.67301e-05 | 0.00289219 | intron-variant | CDC20B | GRCh38.p7 | 5:55140298 | AGGAAAGAAGGACAA[A/T]GTCTTGATCCTGTAC | 166979 |
| rs747868414 | snp | A/G | 1.66421e-05 | 0.00288458 | utr-variant-5-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160160 | CCTCCTTGAATTCCA[A/G]GCTGCTGAGACTTCC | 166979 |
| rs747924764 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55139797 | TGGGAGGCTGAGGCA[A/G]GAGGGTCACTTGCGG | 166979 |
| rs747976414 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55138002 | GTCAAGTTCCCACAC[A/G]TACACACACACCCTG | 166979 |
| rs747984980 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55152805 | TACTATCCTCGGGAC[A/G]TTGGTATCTAGAAAC | 166979 |
| rs748080150 | snp | C/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55166664 | ATCTTCCTTCAGTCT[C/T]GTTTCTGCATCAAAA | 166979 |
| rs748091436 | snp | C/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55132879 | TCTATACCTTTCCAA[C/G]TTCTAATGATCTTCC | 166979 |
| rs748116618 | snp | A/G | 4.94279e-05 | 0.00497107 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55124902 | TCCATCACTGCAGCC[A/G]CTGGAAAGCAGCCTG | 166979 |
| rs748130899 | snp | C/G | 1.65748e-05 | 0.00287874 | missense | CDC20B | GRCh38.p7 | 5:55140382 | TGAACCACGTTCTGG[C/G]TTACAAAGAGTTGTT | 166979 |
| rs748176757 | snp | A/T | 4.94947e-05 | 0.00497443 | missense | CDC20B | GRCh38.p7 | 5:55127267 | CTTACCTGCTGAGGA[A/T]AAAGTGATTCCAGCT | 166979 |
| rs748213686 | in-del | -/A | | | intron-variant, utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55137178 | CGAGACTCTGTCTCA[-/A]AAAAAAAAAAAAAAA | 166979 |
| rs748264217 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55115070 | GCCTTCCCCCAGAAG[C/T]ATCCCACTGGGCCCC | 166979 |
| rs748301290 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55141133 | GAACACTTTGGGGGG[C/T]CGTAGGCAGGTGAAT | 166979 |
| rs748305718 | snp | G/T | 8.25369e-05 | 0.00642352 | splice-acceptor-variant | CDC20B | GRCh38.p7 | 5:55114320 | TCTGCCCCTGTGGCC[G/T]GGGGGAAGAAGGAAA | 166979 |
| rs748359366 | snp | C/T | 1.64947e-05 | 0.00287177 | missense, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55161163 | AGGAAGTAGAATCTT[C/T]TGCAAGAAAAAACTA | 166979 |
| rs748377441 | in-del | -/AACAACC | | | downstream-variant-500B | CDC20B | GRCh38.p7 | 5:55112957 | AGGATGTTAAAACAA[-/AACAACC]AACGATTCAAACAGT | 166979 |
| rs748408984 | snp | C/T | 1.65861e-05 | 0.00287972 | missense | CDC20B | GRCh38.p7 | 5:55114249 | ACAGAGGCCGTCCCA[C/T]CAGCTGCAGCAGAAA | 166979 |
| rs748430443 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55139490 | TGTTATTGACAGCTA[C/T]GGAATAAAACATTGG | 166979 |
| rs748468502 | snp | A/G | 1.67245e-05 | 0.00289171 | missense, intron-variant, nc-transcript-variant, splice-acceptor-variant | GPX8, CDC20B | GRCh38.p7 | 5:55161003 | CGGGAGGTTTCACTA[A/G]TTGTAAACGTGGCCA | 166979 |
| rs748510348 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55134009 | GCACACAGACTCCAA[C/T]ACTGGAGTATTGTTA | 166979 |
| rs748574072 | snp | A/T | 1.64765e-05 | 0.00287019 | intron-variant, missense | CDC20B | GRCh38.p7 | 5:55120511 | TCATTCCTCCTCCAA[A/T]GGCAAGGACCCCAGA | 166979 |
| rs748625091 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55149788 | AACAAGAGAGAAGTG[A/G]TGGTTCCAGAACATT | 166979 |
| rs748626382 | snp | C/T | 1.70749e-05 | 0.00292184 | intron-variant | CDC20B | GRCh38.p7 | 5:55125060 | CAAAAAAATTAAGCC[C/T]TGTTGCTACATAAAC | 166979 |
| rs748663556 | snp | A/T | 1.67256e-05 | 0.0028918 | intron-variant, upstream-variant-2KB, nc-transcript-variant | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170702 | TGCTGACTTGACCCA[A/T]GCAGCCAGCTAACAA | 166979 |
| rs748674528 | snp | G/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55149036 | AAGTACAAAAAGATG[G/T]GAGACAGAGACTAAG | 166979 |
| rs748712142 | snp | A/G | 1.69115e-05 | 0.00290782 | intron-variant | CDC20B | GRCh38.p7 | 5:55146601 | TTCACGTTGCAAAAC[A/G]GGGCTGTGGCGTTTG | 166979 |
| rs748744870 | snp | A/T | 1.65231e-05 | 0.00287424 | missense | CDC20B | GRCh38.p7 | 5:55124825 | GCCGTAGACTGGGTT[A/T]TGACTTTCAGCGGTT | 166979 |
| rs748775337 | snp | G/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55147891 | CACAGATGGGGAAGC[G/T]GAGGCCTAGAGAAAG | 166979 |
| rs748792942 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55128068 | ATTCACTCATTTTCT[A/G]TAACTGTACTCTTAA | 166979 |
| rs748798860 | in-del | -/GGT | | | intron-variant | CDC20B | GRCh38.p7 | 5:55129037 | CACCCAGCTAGAAGA[-/GGT]GGTGGTGGTTCATGT | 166979 |
| rs748828749 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55145628 | TGGTGGTTTGGAGCC[C/T]ACTCCCCCATCTCTG | 166979 |
| rs748923654 | snp | A/T | 1.64741e-05 | 0.00286998 | missense | CDC20B | GRCh38.p7 | 5:55146765 | TGCCACCTTGTGGTA[A/T]TGGGGCTACTCGCAA | 166979 |
| rs748934332 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55156743 | GCCGGGCATTTTGGC[A/G]CGTGCCTGTAGTCCC | 166979 |
| rs749098667 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55130163 | AGAAAATAGAAACCA[C/T]AAAACAAAGCTCTAA | 166979 |
| rs749141941 | in-del | -/ATT | | | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55163123 | TAAATTTTAGTTATA[-/ATT]ATTATATTTTTCCTC | 166979 |
| rs749147711 | snp | C/T | 3.33829e-05 | 0.00408538 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55114242 | ATTCCATACAGAGGC[C/T]GTCCCATCAGCTGCA | 166979 |
| rs749189261 | snp | C/T | 1.64779e-05 | 0.00287031 | intron-variant, missense | CDC20B | GRCh38.p7 | 5:55120547 | AGGGACACCAATCCA[C/T]GGCCTTTAAAGTTTC | 166979 |
| rs749191461 | snp | C/T | 0.000187067 | 0.00966946 | intron-variant | CDC20B | GRCh38.p7 | 5:55140280 | GCAGAGAGAGAGGAG[C/T]GCAGGAAAGAAGGAC | 166979 |
| rs749294320 | snp | G/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55127831 | TGGGGAATGACAACT[G/T]TGGTGTAAGAAGAAA | 166979 |
| rs749304957 | snp | A/G | 1.64879e-05 | 0.00287118 | missense, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55161148 | AGCCCCGCCCAAGCA[A/G]GGAAGTAGAATCTTT | 166979 |
| rs749346725 | snp | A/C | 1.73818e-05 | 0.00294798 | intron-variant | CDC20B | GRCh38.p7 | 5:55146580 | CTCTCAGGAATATAT[A/C]TTTTATTCACGTTGC | 166979 |
| rs749399425 | in-del | -/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55117255 | TTTAACTGAAATTTT[-/C]CCCCCCAAAAAAAAT | 166979 |
| rs749470003 | snp | G/T | 1.65132e-05 | 0.00287339 | intron-variant | CDC20B | GRCh38.p7 | 5:55127251 | CTCCAACAAGACGCT[G/T]CTTACCTGCTGAGGA | 166979 |
| rs749560912 | snp | A/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55124789 | GAAACCTAGAAATCT[A/T]TTGGGTTTCTTACCT | 166979 |
| rs749588596 | snp | C/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55166885 | AAATACAAAAATTAG[C/G]CGGGCACGGTGGCAC | 166979 |
| rs749594093 | snp | A/G | 2.41153e-05 | 0.00347233 | utr-variant-5-prime, upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55173005 | TTCCACTCCATCTCC[A/G]GCTGACTTCGCCCTG | 166979 |
| rs749622626 | snp | C/T | 1.72451e-05 | 0.00293637 | intron-variant | CDC20B | GRCh38.p7 | 5:55128630 | GATCTATAAGAAAAG[C/T]ACTTCAAATTAGTAT | 166979 |
| rs749636698 | snp | A/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55132760 | AATCTGTACCCACCT[A/T]TTCACCAGTCCCCAA | 166979 |
| rs749651674 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55148812 | GTACAGGGTTTTACA[C/T]GTTTGTATTTAATCC | 166979 |
| rs749766821 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55146912 | GTGATGCAAAAGTAA[A/G]AATTCCCTATAAGAG | 166979 |
| rs749768291 | snp | A/T | 1.64849e-05 | 0.00287092 | intron-variant | CDC20B | GRCh38.p7 | 5:55120379 | AACTATTTTCACAAG[A/T]TTCCAGAAGATCAAA | 166979 |
| rs749773363 | snp | C/G | 1.65457e-05 | 0.00287621 | intron-variant, nc-transcript-variant, downstream-variant-500B | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170591 | CACATATTCAACCAG[C/G]TAACAATACACTGCC | 166979 |
| rs749858659 | snp | C/G | 1.7505e-05 | 0.00295841 | intron-variant, downstream-variant-500B | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170507 | CACACACTAATTACA[C/G]ATTCAGTTACACTCT | 166979 |
| rs749869744 | snp | C/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55169223 | AAGAGGATGTGATTT[C/G]AAAGTAGTAAAATGC | 166979 |
| rs749872111 | in-del | -/TTCA | 3.32618e-05 | 0.00407797 | frameshift-variant | CDC20B | GRCh38.p7 | 5:55124809 | TTTCTTACCTTGACT[-/TTCA]GCCGTAGACTGGGTT | 166979 |
| rs749872654 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55121531 | TTTTTGTTTTTGTGC[A/G]TGTGTTTTATTTGCT | 166979 |
| rs749903636 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55120992 | GAGAAAAGAGAACTA[C/T]ATGTGATTGCTCACA | 166979 |
| rs749917352 | snp | A/G | | | intron-variant, utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55137075 | TGCCTGTAATCCCAA[A/G]CTGAGACAGGAGAAT | 166979 |
| rs749920650 | snp | A/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55135093 | TGTAACAAATGTACC[A/T]CTCTGGTGGGAGATG | 166979 |
| rs749947383 | snp | A/C | 1.65427e-05 | 0.00287595 | intron-variant, nc-transcript-variant, downstream-variant-500B | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170612 | ATACACTGCCAGCTC[A/C]TCACACACAGGTATC | 166979 |
| rs749968169 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55132204 | TTCTCTTGGAGAAGG[A/C]GCTGAAGGAATAGGG | 166979 |
| rs750071702 | snp | G/T | 1.65334e-05 | 0.00287514 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55140342 | TTCGGATTGCTCACA[G/T]AGCTGCATTTTTCCA | 166979 |
| rs750085969 | snp | A/G | 0.000140598 | 0.00838326 | intron-variant | CDC20B | GRCh38.p7 | 5:55137658 | GAAGGGGAGAGACAT[A/G]GGTAAGTCAAGTCAA | 166979 |
| rs750088272 | snp | G/T | 1.77846e-05 | 0.00298194 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164025 | AAAGAATAAAATTAT[G/T]CTCATGAAAATATGT | 166979 |
| rs750139154 | in-del | -/GAATAA | | | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55162656 | AATGGCAACCACAGT[-/GAATAA]GAGGTCTTTATTCCT | 166979 |
| rs750177762 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55129319 | ACAAACACCTGGAGA[C/T]CCTGTAAAGTAAGGA | 166979 |
| rs750183407 | snp | G/T | 1.64846e-05 | 0.0028709 | missense | CDC20B | GRCh38.p7 | 5:55146654 | GTCTCTTTCTCAGGC[G/T]GTGTCTTCAGCACTG | 166979 |
| rs750204423 | in-del | -/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55125537 | TAAAGAACTAAACTT[-/C]TTTGTAAAAGAAGTT | 166979 |
| rs750204481 | in-del | -/A | 0.00252716 | 0.0354569 | intron-variant | CDC20B | GRCh38.p7 | 5:55128399 | AGAGAACATGATGAG[-/A]AAAAAAAAAACTGGC | 166979 |
| rs750233266 | snp | G/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55117294 | TGGTTAACAGGGTAC[G/T]GCTTAGTAAAGGTGT | 166979 |
| rs750236059 | snp | C/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55146182 | TGAAAGCCTAACTTA[C/G]CTGAGTCTCCGCCAA | 166979 |
| rs750289012 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55145201 | CTTTCAGAAGATAGT[C/T]ATAACAATGTTTTTC | 166979 |
| rs750342029 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55157447 | GGTTAATGGGTCAGT[A/G]TGAAAATTTATATAT | 166979 |
| rs750368816 | snp | C/T | 1.69109e-05 | 0.00290778 | missense | CDC20B | GRCh38.p7 | 5:55114235 | AGTAGCAATTCCATA[C/T]AGAGGCCGTCCCATC | 166979 |
| rs750370791 | snp | A/G | 8.24994e-05 | 0.00642206 | missense | CDC20B | GRCh38.p7 | 5:55127348 | TAGTTACCACATCCC[A/G]TAACTGAAAAAATGA | 166979 |
| rs750381723 | snp | A/G | | | intron-variant, upstream-variant-2KB, downstream-variant-500B | CDC20B, MIR449A, MIR449B, MIR449C | GRCh38.p7 | 5:55171820 | GTGTTGTCCAGGCTG[A/G]TCTTGAAGTCTTGGC | 166979 |
| rs750400855 | snp | A/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55114865 | ATTTCCAGATCCTTA[A/T]TGACATCTCCAAATG | 166979 |
| rs750412123 | in-del | -/GAAA | 1.80605e-05 | 0.00300498 | intron-variant | CDC20B | GRCh38.p7 | 5:55146890 | GCTGTAAGTCCACTG[-/GAAA]GCCTCAGTGATGCAA | 166979 |
| rs750440906 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55143311 | TAATCCCAACTCAAC[A/G]TTTTCTCATATATTT | 166979 |
| rs750562424 | snp | A/T | 1.66134e-05 | 0.00288208 | intron-variant | CDC20B | GRCh38.p7 | 5:55119954 | AGAGAATTCTTGCAA[A/T]TTCTGATTCCTTATG | 166979 |
| rs750592577 | snp | G/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55165523 | TTTCGTATGGCAAAT[G/T]CAGTAATGCTACCTC | 166979 |
| rs750625976 | snp | A/G | 1.65858e-05 | 0.00287969 | intron-variant, upstream-variant-2KB, nc-transcript-variant | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170674 | CAGAAGCAAGTGGCA[A/G]GGTAGTTGTGGCTGC | 166979 |
| rs750666930 | snp | C/T | 1.65499e-05 | 0.00287657 | intron-variant, nc-transcript-variant, downstream-variant-500B | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170572 | CATGTTAGCCGATGC[C/T]ATTCACATATTCAAC | 166979 |
| rs750751058 | snp | G/T | 4.3928e-05 | 0.00468637 | intron-variant, upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55172928 | GAATGCAGAAAAGGG[G/T]GTTACTCACCCACAG | 166979 |
| rs750819530 | snp | A/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55140500 | ATTACAACTGGTAAT[A/T]CACTAAGGAGTTCAA | 166979 |
| rs750851148 | snp | A/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55124159 | ATGGTGGAGCATTGA[A/T]CTAATTCCACAGCAC | 166979 |
| rs750870845 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55154958 | CTGCAGTGAAGGAAA[C/T]ACTGCTGCAGATTGT | 166979 |
| rs750935532 | snp | A/G | 1.69192e-05 | 0.00290849 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55128616 | ATCTAGGATATTCAG[A/G]TCTATAAGAAAAGCA | 166979 |
| rs751028279 | in-del | -/AA | | | intron-variant | CDC20B | GRCh38.p7 | 5:55129261 | CCCCTACAATACATT[-/AA]CCGTCCCCATGATAA | 166979 |
| rs751060772 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55150216 | AATCTTTTTAAAAAT[A/G]GTAACATAGGATAAT | 166979 |
| rs751137374 | snp | C/G | 1.64942e-05 | 0.00287173 | missense, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55161074 | GGAACTGCACAAAGA[C/G]TTTGGACCATCCCAC | 166979 |
| rs751148673 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55148769 | ACATCCAGCATTTAT[C/T]GAGTAGTTACTATGT | 166979 |
| rs751164251 | snp | C/T | 1.65707e-05 | 0.00287838 | intron-variant | CDC20B | GRCh38.p7 | 5:55127211 | CTCAGGCCCCATAAT[C/T]AATTGTTAATACAAA | 166979 |
| rs751222823 | snp | A/G | 4.957e-05 | 0.00497821 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55133470 | TTGGAGTATGGAATC[A/G]TTTATATCACCAGAA | 166979 |
| rs751225085 | in-del | -/A | | | intron-variant | CDC20B | GRCh38.p7 | 5:55154611 | AAAAACTTACTTTAT[-/A]TTGCTCCCTGTGATA | 166979 |
| rs751241308 | snp | A/T | 1.82377e-05 | 0.00301969 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160944 | ACTTGCAGAATTTTT[A/T]AAAATCTTTTGCTTC | 166979 |
| rs751311156 | in-del | -/TA | 1.64855e-05 | 0.00287097 | frameshift-variant, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160271 | TGCTGTCTATAGTTC[-/TA]TATGCACAGTAACGC | 166979 |
| rs751341540 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55120616 | ACTCATGAATGTGAT[A/G]CACTTAGGTAAGCAG | 166979 |
| rs751356503 | snp | A/G | 4.96619e-05 | 0.00498282 | intron-variant, nc-transcript-variant, downstream-variant-500B | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170567 | AGTTGCATGTTAGCC[A/G]ATGCCATTCACATAT | 166979 |
| rs751371490 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55140470 | GTACAACTAAAATGT[A/G]ATGTATAATATAGAA | 166979 |
| rs751417640 | in-del | -/G | 0.000294942 | 0.0121402 | intron-variant, upstream-variant-2KB, downstream-variant-500B | CDC20B, MIR449A, MIR449B, MIR449C | GRCh38.p7 | 5:55172252 | CATTTCCATTTCTTT[-/G]GGGGGGCGTGCTTCT | 166979 |
| rs751436304 | snp | C/G | | | intron-variant, upstream-variant-2KB | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55171592 | CAATATAGGATGTTA[C/G]CACTTGAATACTGAA | 166979 |
| rs751438674 | snp | G/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55134721 | GCCTGGGTGACAGAG[G/T]GAGGTTCTGTCTCTA | 166979 |
| rs751450749 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55156467 | ATTCTTCATTGTTCC[A/G]TTCACTAATTCTGTG | 166979 |
| rs751541942 | snp | A/G | 1.64898e-05 | 0.00287135 | synonymous-codon, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160219 | TGCAGCTTACCCGCT[A/G]AAATGTTCCGGGCCC | 166979 |
| rs751554659 | snp | C/T | 5.11635e-05 | 0.00505758 | intron-variant | CDC20B | GRCh38.p7 | 5:55143662 | CAAGAAAGACATTTA[C/T]CTTTGAATTTGGTTT | 166979 |
| rs751567146 | snp | A/C | 0.000843407 | 0.0205181 | intron-variant, utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55137568 | GAGTATTCAGAGGGC[A/C]TCTCAATTAGTCTTT | 166979 |
| rs751585333 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55165372 | AAATATACATTCATC[A/G]CATAAAAGAATTAAA | 166979 |
| rs751695343 | snp | C/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55128930 | TCGTTTAACGGATCA[C/G]TAAAAGTTAAAAGCA | 166979 |
| rs751764261 | snp | C/T | 1.65551e-05 | 0.00287702 | intron-variant | CDC20B | GRCh38.p7 | 5:55119938 | AATAATGATCAAAAA[C/T]AGAGAATTCTTGCAA | 166979 |
| rs751782825 | snp | C/T | 1.65488e-05 | 0.00287647 | intron-variant | CDC20B | GRCh38.p7 | 5:55119784 | GTGCATGGCATTTTA[C/T]TCACCCATTTGCTTA | 166979 |
| rs751804749 | snp | A/G | 1.79965e-05 | 0.00299965 | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164261 | GAGAAATGTCTCCAT[A/G]AGGGTTTGGTCTCAT | 166979 |
| rs751900387 | snp | C/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55118534 | ATCCTATCACATGCC[C/G]CCACCTAGCTGAAGG | 166979 |
| rs751914852 | snp | A/C | 1.648e-05 | 0.0028705 | missense | CDC20B | GRCh38.p7 | 5:55124873 | CCTGGATCGTGGGGC[A/C]ATATTGTCAGCAGTC | 166979 |
| rs751926266 | in-del | -/A | | | intron-variant | CDC20B | GRCh38.p7 | 5:55147423 | TGTTATATTTTATAT[-/A]ATTTTTATATTGATA | 166979 |
| rs751945181 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55139023 | ATCTCCAAGAATGAA[A/G]ATATCCACCAATGGG | 166979 |
| rs751945761 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55151760 | CCACCTTCACTTCTG[A/G]GTTCAGCCATCAACT | 166979 |
| rs752044192 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55166440 | AAGCAGAGTAGGCAG[A/G]AGGAGATTTGAAAGC | 166979 |
| rs752072874 | snp | C/G | 1.66382e-05 | 0.00288424 | missense | CDC20B | GRCh38.p7 | 5:55146850 | TAGCATTAACTGAAT[C/G]GAGTACCTGTTTAAC | 166979 |
| rs752136177 | snp | C/T | 1.6477e-05 | 0.00287024 | missense | CDC20B | GRCh38.p7 | 5:55124957 | CACACAGCTTGCTTG[C/T]GGCGAAGTGTTCCAA | 166979 |
| rs752200049 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55148650 | CTGCAGTGAGCCGCA[C/T]TGGCGCTGCTGCACT | 166979 |
| rs752260258 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55125300 | ATCTGATGTAAGCAG[C/T]GATGGAAAAATAAGC | 166979 |
| rs752298135 | snp | C/T | | | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55159213 | TAGAGACAGGGGTAT[C/T]GCTTTCTTGCCCAAG | 166979 |
| rs752303866 | snp | C/G | 6.78311e-05 | 0.00582331 | intron-variant | CDC20B | GRCh38.p7 | 5:55143654 | GGATCCTACAAGAAA[C/G]ACATTTATCTTTGAA | 166979 |
| rs752351724 | snp | G/T | | | upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55174150 | CCCCCCAACCATTTT[G/T]GACATTGGATTGTAT | 166979 |
| rs752420199 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55155300 | ACAACTGAGAAAATA[A/G]AAACAAATATGTCTA | 166979 |
| rs752426834 | snp | C/G/T | 4.96006e-05 | 0.00497978 | missense | CDC20B | GRCh38.p7 | 5:55125011 | TCGTGATGATAAACA[C/G/T]GCCCCAGTCTTGACC | 166979 |
| rs752442856 | snp | C/T | 0.000131942 | 0.00812117 | missense, upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55172948 | CTCACCCACAGCATC[C/T]CCTCTTCCGTGCGGA | 166979 |
| rs752466825 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55133281 | AAGTATATTAGCCAT[A/G]TTTGGATGCTACACT | 166979 |
| rs752485138 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55167813 | AGGCTGCAGTGAGCC[A/G]ACATGGCTCCACTGA | 166979 |
| rs752490660 | snp | A/G | | | intron-variant, downstream-variant-500B | CDC20B, MIR449A | GRCh38.p7 | 5:55170069 | CAGTGAGCCGAGATC[A/G]CGCCACTGTACTCCA | 166979 |
| rs752501343 | snp | A/C | 1.64727e-05 | 0.00286986 | missense, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164073 | CTTCAAAGAAGGAAC[A/C]AAGGTGGAATTTTTG | 166979 |
| rs752577948 | snp | A/G | 0.000149694 | 0.00865013 | intron-variant | CDC20B | GRCh38.p7 | 5:55119765 | ACAGCTCACTTTGCT[A/G]TAGGTGCATGGCATT | 166979 |
| rs752689917 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55144215 | TGCAGAAAGATGTTT[C/T]AAAGATAGTTTAAGA | 166979 |
| rs752697463 | snp | A/G | 1.73899e-05 | 0.00294867 | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164240 | CATTGCGTTTCTAAT[A/G]GAACAGAGAAATGTC | 166979 |
| rs752722569 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55143900 | CTCAATGAGAAAGCT[A/G]TCTCAGTGGCCTCTA | 166979 |
| rs752729498 | snp | C/T | 1.64743e-05 | 0.00287 | missense | CDC20B | GRCh38.p7 | 5:55146744 | AGAGCCCTAGTTTGA[C/T]TTTGCTGCCACCTTG | 166979 |
| rs752898648 | snp | C/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55156199 | TATTCACTACCACAA[C/G]AACAGTATAGGGGTA | 166979 |
| rs752923802 | snp | C/G/T | 6.60081e-05 | 0.00574459 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55146833 | CTTAAAGTCAGAATA[C/G/T]GTAGCATTAACTGAA | 166979 |
| rs752953222 | snp | A/C | 0.000140598 | 0.00838326 | intron-variant, stop-lost | CDC20B | GRCh38.p7 | 5:55137577 | GAGGGCCTCTCAATT[A/C]GTCTTTGCCACCAAC | 166979 |
| rs752958395 | in-del | -/AA | | | intron-variant | CDC20B | GRCh38.p7 | 5:55128261 | TAAAAACCATTCAGT[-/AA]AAAAAAAAAAAAAAA | 166979 |
| rs753077122 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55129255 | GTTTAAACCCCTACA[A/G]TACATTCCGTCCCCA | 166979 |
| rs753099157 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55135310 | AGAATAATATAGGTA[C/T]ATTATCTCTGGCTTC | 166979 |
| rs753153188 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55165246 | TCACTGAACCTCTTA[A/G]AGTCACAAGGCATTT | 166979 |
| rs753161232 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55150454 | CAGGGGGCGAGGCCG[A/G]CTCTCTCTCCACTGC | 166979 |
| rs753206779 | snp | A/G | | | downstream-variant-500B | CDC20B | GRCh38.p7 | 5:55112602 | CTGTGGCTTTCAGTG[A/G]CCTAAAATTTTCTAA | 166979 |
| rs753219788 | snp | A/G | 0.000287068 | 0.0119771 | intron-variant, upstream-variant-2KB, nc-transcript-variant | CDC20B, MIR449A, MIR449B, MIR449C | GRCh38.p7 | 5:55172309 | GCAACTGTTAAAATC[A/G]TTAACAGCCGCTAGC | 166979 |
| rs753242954 | snp | C/T | 4.94515e-05 | 0.00497225 | missense | CDC20B | GRCh38.p7 | 5:55124865 | CACTGGCACCTGGAT[C/T]GTGGGGCCATATTGT | 166979 |
| rs753250135 | snp | A/G | 6.62098e-05 | 0.00575331 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55140330 | TTTCCAAACACATTC[A/G]GATTGCTCACAGAGC | 166979 |
| rs753261283 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55128916 | AGTACATGTAGACTT[C/T]GTTTAACGGATCAGT | 166979 |
| rs753297920 | snp | C/T | 1.65362e-05 | 0.00287538 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55140372 | ATTAGCCTGCTGAAC[C/T]ACGTTCTGGGTTACA | 166979 |
| rs753323194 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55122551 | TCCATCAATAGGTAC[A/C]ATCTAATTCCTCTAC | 166979 |
| rs753385316 | snp | C/G | | | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55159065 | TCTCACTCTGTCACC[C/G]AGGCTGCAGTCTACA | 166979 |
| rs753494760 | snp | A/T | 3.43312e-05 | 0.004143 | intron-variant | CDC20B | GRCh38.p7 | 5:55143482 | CAGCTTCTCTAGATG[A/T]GGGATCTTCAGTTTT | 166979 |
| rs753528964 | snp | A/T | 0.000214195 | 0.0103466 | intron-variant, upstream-variant-2KB | CDC20B, MIR449B, MIR449C | GRCh38.p7 | 5:55172663 | TTCCTTTGAAAACAC[A/T]GATAACATATTGAGG | 166979 |
| rs753553887 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55165238 | ATCAGCAGTCACTGA[A/G]CCTCTTAGAGTCACA | 166979 |
| rs753597771 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55148376 | AAAGCCTTCATATAT[A/G]TGCATAACTTCTACT | 166979 |
| rs753610630 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55134653 | TGTAGTCCCAGCTAC[C/T]TGGGTGGCTTAGGTG | 166979 |
| rs753662167 | snp | C/T | 1.66382e-05 | 0.00288424 | intron-variant | CDC20B | GRCh38.p7 | 5:55114370 | CGTTACATGGGCTGC[C/T]GCTCAGGACTGTAGG | 166979 |
| rs753720234 | snp | A/G | 1.65493e-05 | 0.00287652 | intron-variant | CDC20B | GRCh38.p7 | 5:55127381 | AAGGAGAGTTATGTA[A/G]CATTGGAGTTTTCAC | 166979 |
| rs753740797 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55146287 | GTAGCCAATCAGGCC[A/G]GCTCCTACGCACTTC | 166979 |
| rs753750257 | snp | G/T | 1.6825e-05 | 0.00290038 | intron-variant | CDC20B | GRCh38.p7 | 5:55128413 | GAAAAAAAAAAACTG[G/T]CCAGTACTTGCACTT | 166979 |
| rs753856615 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55120350 | AGCTTGTTGGGGGCA[C/T]AGGCTCTGTTGTAAA | 166979 |
| rs753861241 | snp | C/G | 1.64931e-05 | 0.00287163 | missense | CDC20B | GRCh38.p7 | 5:55114309 | AGGTGCAGCACTCTG[C/G]CCCTGTGGCCTGGGG | 166979 |
| rs753869301 | snp | C/T | | | upstream-variant-2KB | CDC20B | GRCh38.p7 | 5:55174557 | AAAAGTAAACTATTA[C/T]TGGATGAGAGTCAGA | 166979 |
| rs753874504 | snp | A/G | 1.66394e-05 | 0.00288434 | intron-variant, upstream-variant-2KB, nc-transcript-variant | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170691 | GTAGTTGTGGCTGCT[A/G]ACTTGACCCAAGCAG | 166979 |
| rs753909098 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55140981 | CATAGTGATAAATGA[C/T]TAAAGCAGAGAAGAT | 166979 |
| rs753966534 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55155092 | AAAGGAAGAGGAAGA[C/T]AAGAAAAGTAAGACA | 166979 |
| rs753974530 | snp | A/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55118813 | CAGTCGGGCTCATCA[A/T]CAGAGGCAGGAAGTC | 166979 |
| rs754011660 | snp | C/T | 3.79845e-05 | 0.00435785 | intron-variant | CDC20B | GRCh38.p7 | 5:55124754 | TATGTGAAGGATACC[C/T]AGTGGCCTCTGAGTA | 166979 |
| rs754013351 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55166546 | GCTGAGAGAGGGAGC[A/G]GAGTCATTTGCTGAT | 166979 |
| rs754016445 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55154140 | AGAGACCACAGTGAC[A/G]GGGGTCAAGGTAAAC | 166979 |
| rs754021604 | snp | C/T | 1.64811e-05 | 0.00287059 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55146665 | AGGCGGTGTCTTCAG[C/T]ACTGATCCGGAAGCT | 166979 |
| rs754045599 | snp | A/G | | | intron-variant, downstream-variant-500B | GPX8, CDC20B | GRCh38.p7 | 5:55167582 | GTGATAATTGGTGAT[A/G]GGCATGATGGCTCAG | 166979 |
| rs754055273 | snp | A/G | 1.64743e-05 | 0.00287 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55146722 | TTCCCCAAAGGAATC[A/G]GAGGACAGAGCCCTA | 166979 |
| rs754103375 | snp | C/T | 1.68227e-05 | 0.00290018 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160402 | TAAAGGCAAAGTAAG[C/T]TGCATCATCTGATTT | 166979 |
| rs754167300 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55117557 | TTTGAAGACCCTGAT[A/C]CAGATCTCAGTCATC | 166979 |
| rs754182483 | snp | A/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55125738 | ATGTTCCACAATTAT[A/T]TCAGACATTTCTCAA | 166979 |
| rs754236175 | snp | A/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55125528 | TAGTTTTGCTAAAGA[A/T]CTAAACTTCTTTGTA | 166979 |
| rs754252902 | snp | C/T | | | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55163829 | CTTCATTTCTTGATA[C/T]TAAGATCACATACTA | 166979 |
| rs754285964 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55142839 | GCATACACTGAATAA[A/G]TAATTTTGCCTAAAT | 166979 |
| rs754387660 | snp | A/C | 0.000220653 | 0.0105013 | intron-variant, utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55137560 | CTTGCATAGAGTATT[A/C]AGAGGGCCTCTCAAT | 166979 |
| rs754387691 | snp | C/T | 1.64773e-05 | 0.00287026 | intron-variant, synonymous-codon | CDC20B | GRCh38.p7 | 5:55120494 | GTGTAAGCGTCCATC[C/T]TTCATTCCTCCTCCA | 166979 |
| rs754389124 | snp | G/T | 0.000154238 | 0.00878038 | intron-variant | CDC20B | GRCh38.p7 | 5:55143485 | CTTCTCTAGATGTGG[G/T]ATCTTCAGTTTTTTT | 166979 |
| rs754429323 | snp | A/C | 1.6477e-05 | 0.00287024 | missense | CDC20B | GRCh38.p7 | 5:55124888 | CATATTGTCAGCAGT[A/C]CATCACTGCAGCCGC | 166979 |
| rs754452037 | snp | A/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55145548 | AAATGAGAATTACAT[A/T]TTTCAGAAAGAGAGT | 166979 |
| rs754523754 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55148049 | TTATCTTTTAATAAA[A/G]TGACAGACAATTTAG | 166979 |
| rs754530404 | snp | A/G | 1.64798e-05 | 0.00287047 | intron-variant, upstream-variant-2KB | CDC20B, MIR449B, MIR449C | GRCh38.p7 | 5:55172665 | CCTTTGAAAACACAG[A/G]TAACATATTGAGGGA | 166979 |
| rs754589469 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55121344 | TAAACAGTTTTCCAC[A/G]TTTTAATAGACTTTT | 166979 |
| rs754613277 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55122566 | AATCTAATTCCTCTA[C/T]CTTTGAATGTGGGAC | 166979 |
| rs754663488 | snp | C/T | 1.64955e-05 | 0.00287184 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55114311 | GTGCAGCACTCTGCC[C/T]CTGTGGCCTGGGGGA | 166979 |
| rs754667951 | in-del | -/TA | 3.29579e-05 | 0.00405929 | frameshift-variant | CDC20B | GRCh38.p7 | 5:55128514 | AGTGAGACTTAAGTC[-/TA]TGTTTTCAATCCCAT | 166979 |
| rs754686056 | in-del | -/AATC | 1.64852e-05 | 0.00287094 | frameshift-variant, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160321 | ATTCCTCAAACCTAA[-/AATC]AACAGCTTTTATGCC | 166979 |
| rs754724476 | snp | A/C | 3.29843e-05 | 0.00406092 | missense, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55161157 | CAAGCAAGGAAGTAG[A/C]ATCTTTTGCAAGAAA | 166979 |
| rs754747877 | snp | C/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55166589 | GTAACTCAAATGCCT[C/T]ATAGGAATACCAGCG | 166979 |
| rs754755397 | snp | G/T | 3.31395e-05 | 0.00407046 | intron-variant | CDC20B | GRCh38.p7 | 5:55127390 | TATGTAGCATTGGAG[G/T]TTTCACAGCCCACTG | 166979 |
| rs754786997 | snp | G/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55134725 | GGGTGACAGAGTGAG[G/T]TTCTGTCTCTAAAAA | 166979 |
| rs754884523 | snp | G/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55116147 | ACTCCAAACCCTGAT[G/T]AAAGAATCTCTTTTT | 166979 |
| rs754920635 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55148445 | TCAGCCGGCCGTGGC[A/G]GCTCATGCTTGAAAT | 166979 |
| rs754942770 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55131058 | GCCCAGGAGGTAGAG[A/G]CCACAGTAAGCCTCT | 166979 |
| rs754992563 | snp | A/G | 1.7031e-05 | 0.00291808 | missense, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164055 | TTCTGGATATTTTAG[A/G]TTCTTCAAAGAAGGA | 166979 |
| rs755002663 | snp | C/G | 1.66663e-05 | 0.00288667 | intron-variant | CDC20B | GRCh38.p7 | 5:55119758 | CCCAACAACAGCTCA[C/G]TTTGCTATAGGTGCA | 166979 |
| rs755037794 | snp | C/T | 8.23974e-05 | 0.00641809 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55146668 | CGGTGTCTTCAGCAC[C/T]GATCCGGAAGCTTCT | 166979 |
| rs755045883 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55115037 | AATGACAGTGCTATG[C/T]TCCTGCCACATATCC | 166979 |
| rs755056119 | snp | A/C | 1.66891e-05 | 0.00288864 | intron-variant, upstream-variant-2KB, nc-transcript-variant | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170698 | TGGCTGCTGACTTGA[A/C]CCAAGCAGCCAGCTA | 166979 |
| rs755107496 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55141049 | CAAATATGACAAACA[C/T]TGTGTCAGGTTCAGA | 166979 |
| rs755116074 | in-del | -/TTTTAAT | | | intron-variant | CDC20B | GRCh38.p7 | 5:55138766 | GAGTACAGAAATTGC[-/TTTTAAT]TTTTAAAAAATTAAA | 166979 |
| rs755160394 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55155131 | AAAAGGGATGAATGA[A/C]TCGGTACTCCAAGCA | 166979 |
| rs755187644 | snp | A/G | | | intron-variant, downstream-variant-500B | GPX8, CDC20B | GRCh38.p7 | 5:55167636 | CAGCTGAGGTGGGAG[A/G]ATCACTTGAGCCCAG | 166979 |
| rs755188682 | snp | C/T | | | upstream-variant-2KB | CDC20B | GRCh38.p7 | 5:55174820 | TTTAGAATGCAATTA[C/T]CTGTAAAAATACATT | 166979 |
| rs755234113 | snp | A/G | 1.64746e-05 | 0.00287002 | missense | CDC20B | GRCh38.p7 | 5:55146723 | TCCCCAAAGGAATCA[A/G]AGGACAGAGCCCTAG | 166979 |
| rs755238387 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55149732 | GGAGCAACTGCTTAA[C/T]GGGTATGGAGTTTTC | 166979 |
| rs755267716 | snp | A/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55117570 | ATCCAGATCTCAGTC[A/T]TCAGGTGTATGTCAA | 166979 |
| rs755272178 | snp | C/G | 3.30207e-05 | 0.00406316 | splice-donor-variant | CDC20B | GRCh38.p7 | 5:55127256 | ACAAGACGCTTCTTA[C/G]CTGCTGAGGATAAAG | 166979 |
| rs755341204 | snp | A/G | 1.65299e-05 | 0.00287483 | missense | CDC20B | GRCh38.p7 | 5:55133459 | TTCACCTCTGGTTGG[A/G]GTATGGAATCGTTTA | 166979 |
| rs755348866 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55125891 | AGGCTAGTGTCTTAG[C/T]TTAATTTGAAAAAAC | 166979 |
| rs755387996 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55126836 | GAACAGGATAATCTA[C/T]GAGGTTCCTTCTGCT | 166979 |
| rs755405005 | snp | A/G | 1.71226e-05 | 0.00292592 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160414 | AAGTTGCATCATCTG[A/G]TTTTTATTGTTATCA | 166979 |
| rs755425226 | snp | C/T | 1.78372e-05 | 0.00298635 | intron-variant | CDC20B | GRCh38.p7 | 5:55128651 | AAATTAGTATAATTA[C/T]ACAGCCACATGAAAA | 166979 |
| rs755430105 | snp | C/G | 1.65438e-05 | 0.00287605 | intron-variant, nc-transcript-variant, downstream-variant-500B | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170602 | CCAGCTAACAATACA[C/G]TGCCAGCTCATCACA | 166979 |
| rs755487738 | snp | A/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55150189 | ATATGTGCATTTCAC[A/T]TCAATAAAAGAAATC | 166979 |
| rs755522152 | snp | C/T | 3.75827e-05 | 0.00433474 | intron-variant | CDC20B | GRCh38.p7 | 5:55124764 | ATACCCAGTGGCCTC[C/T]GAGTAACAGGAAACC | 166979 |
| rs755580048 | snp | G/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55156595 | AAACATAAGTCACTG[G/T]CCAGGCATGGTGGCT | 166979 |
| rs755605716 | snp | C/T | 1.77263e-05 | 0.00297705 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164027 | AGAATAAAATTATGC[C/T]CATGAAAATATGTTC | 166979 |
| rs755607697 | snp | A/G | 3.40454e-05 | 0.00412572 | intron-variant | CDC20B | GRCh38.p7 | 5:55140276 | GGAGGCAGAGAGAGA[A/G]GAGCGCAGGAAAGAA | 166979 |
| rs755610525 | snp | A/C | 1.64768e-05 | 0.00287021 | intron-variant, stop-gained | CDC20B | GRCh38.p7 | 5:55120502 | GTCCATCCTTCATTC[A/C]TCCTCCAATGGCAAG | 166979 |
| rs755624010 | snp | C/T | 1.64863e-05 | 0.00287104 | missense, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55161111 | GTGTTGGCTTTTCCC[C/T]GCAATCAGTTTGGAG | 166979 |
| rs755647760 | in-del | -/T | 1.64905e-05 | 0.00287141 | frameshift-variant, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160346 | TTTATGCCTTTGAAG[-/T]TGAAGGATGCAAAAG | 166979 |
| rs755686237 | in-del | -/A | | | upstream-variant-2KB | CDC20B | GRCh38.p7 | 5:55175105 | TTAAACACAAAAAAT[-/A]AAAATCACAACTTTT | 166979 |
| rs755749740 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55133954 | AAATATTTATTGATT[C/T]GTTGATTTTAGCTCT | 166979 |
| rs755762320 | snp | C/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55132235 | AGATAGAGAACTGTT[C/G]CCTTCAGGGATTTTT | 166979 |
| rs755801919 | snp | C/T | 1.65315e-05 | 0.00287498 | missense | CDC20B | GRCh38.p7 | 5:55140346 | GATTGCTCACAGAGC[C/T]GCATTTTTCCATTAG | 166979 |
| rs755807362 | in-del | -/AA | 4.94189e-05 | 0.00497062 | frameshift-variant, upstream-variant-2KB | CDC20B, MIR449A, MIR449B, MIR449C | GRCh38.p7 | 5:55172619 | CTTCTCTTCTGCTTC[-/AA]GTCTTTGGAGAGCAC | 166979 |
| rs755820628 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55150359 | GAATATGCTAGAATG[C/T]TGAAGCAGTAAGCAT | 166979 |
| rs755890847 | snp | G/T | 3.29658e-05 | 0.00405978 | missense | CDC20B | GRCh38.p7 | 5:55146655 | TCTCTTTCTCAGGCG[G/T]TGTCTTCAGCACTGA | 166979 |
| rs755912246 | snp | A/G | 1.65162e-05 | 0.00287365 | intron-variant | CDC20B | GRCh38.p7 | 5:55127248 | TGTCTCCAACAAGAC[A/G]CTTCTTACCTGCTGA | 166979 |
| rs756000192 | snp | G/T | 1.67466e-05 | 0.00289362 | intron-variant | CDC20B | GRCh38.p7 | 5:55125035 | CTTGACCCACTGCGA[G/T]TTTACATAACAAAAA | 166979 |
| rs756024821 | snp | C/G | | | synonymous-codon | CDC20B | GRCh38.p7 | 5:55143525 | TACCTGCCCTTTTGA[C/G]GCAACACTTTCTTTC | 166979 |
| rs756055799 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55122468 | ATTCTGCGGCAGATT[A/G]TATTTTCCAAAGATA | 166979 |
| rs756082974 | snp | A/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55145312 | CATTGATTTGAAAAA[A/T]ATCTGGGCTCCCTTT | 166979 |
| rs756103007 | snp | C/T | 1.64849e-05 | 0.00287092 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55114281 | CACCCGGGTCTGGTC[C/T]GGACTCAAAGACAGG | 166979 |
| rs756173688 | snp | G/T | 1.66768e-05 | 0.00288758 | intron-variant | CDC20B | GRCh38.p7 | 5:55119962 | CTTGCAATTTCTGAT[G/T]CCTTATGAATATAGT | 166979 |
| rs756213919 | snp | C/T | 9.92884e-05 | 0.00704517 | intron-variant, nc-transcript-variant, downstream-variant-500B | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170574 | TGTTAGCCGATGCCA[C/T]TCACATATTCAACCA | 166979 |
| rs756301067 | snp | A/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55152254 | CCGTAACTAGAAGAG[A/T]ATATGTGTGTCTAAG | 166979 |
| rs756339337 | snp | C/T | 8.29993e-05 | 0.00644149 | intron-variant, upstream-variant-2KB, nc-transcript-variant | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170680 | CAAGTGGCAGGGTAG[C/T]TGTGGCTGCTGACTT | 166979 |
| rs756356113 | snp | C/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55165557 | ATATAGTTCTGTATA[C/T]GTATTTGGACCAAAG | 166979 |
| rs756363853 | snp | A/T | 4.94768e-05 | 0.00497352 | missense, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55161159 | AGCAAGGAAGTAGAA[A/T]CTTTTGCAAGAAAAA | 166979 |
| rs756429156 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55123829 | CTGGGAATTTGGACC[A/G]ATCATCATTCTCAAT | 166979 |
| rs756533027 | snp | A/G | 1.64846e-05 | 0.0028709 | intron-variant, upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55172932 | GCAGAAAAGGGTGTT[A/G]CTCACCCACAGCATC | 166979 |
| rs756552017 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55140713 | TCTGTTTAGCCTATA[C/T]ACCATAGGCCAGTGA | 166979 |
| rs756597778 | in-del | -/AGTTGAGGTGAGG | | | intron-variant | CDC20B | GRCh38.p7 | 5:55151949 | TTCAGGATGAAGTTA[-/AGTTGAGGTGAGG]AGACTATTGTGAATT | 166979 |
| rs756606380 | snp | C/G | | | missense | CDC20B | GRCh38.p7 | 5:55146768 | CACCTTGTGGTAATG[C/G]GGCTACTCGCAACAG | 166979 |
| rs756672503 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55139491 | GTTATTGACAGCTAC[A/G]GAATAAAACATTGGA | 166979 |
| rs756750217 | snp | A/T | 5.4761e-05 | 0.00523235 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160945 | CTTGCAGAATTTTTT[A/T]AAATCTTTTGCTTCA | 166979 |
| rs756763772 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55129262 | CCCCTACAATACATT[A/C]CGTCCCCATGATAAA | 166979 |
| rs756767626 | snp | C/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55168010 | TTGATTTGTGGTGTT[C/G]CTTTGAAAGAAAAAT | 166979 |
| rs756797866 | snp | C/G | | | intron-variant, missense | CDC20B | GRCh38.p7 | 5:55137634 | TGCTGCCACTAAAGT[C/G]ATCTATGGGAAGGGG | 166979 |
| rs756807164 | in-del | -/AAA | | | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55162091 | TAAACCATATTAGTC[-/AAA]AAAAAAAAAAAAAAA | 166979 |
| rs756845368 | snp | C/T | 1.65633e-05 | 0.00287774 | intron-variant | CDC20B | GRCh38.p7 | 5:55127223 | AATCAATTGTTAATA[C/T]AAACATAACTGTCTC | 166979 |
| rs756916125 | snp | G/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55149594 | TTATGCTAAGTGAAA[G/T]AAGCCAGACAGGAAA | 166979 |
| rs756936422 | snp | A/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55148785 | GAGTAGTTACTATGT[A/T]TGAAACCATATGTAC | 166979 |
| rs756951048 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55155153 | CTCCAAGCACATCAG[C/T]TCAGCTTGTTTACCT | 166979 |
| rs757004905 | snp | A/C/T | 3.31034e-05 | 0.00406827 | intron-variant, nc-transcript-variant, downstream-variant-500B | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170569 | TTGCATGTTAGCCGA[A/C/T]GCCATTCACATATTC | 166979 |
| rs757136265 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55120854 | CTACATGCAATACAT[C/T]CTATGGGGCAAAAAT | 166979 |
| rs757181931 | snp | G/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55157200 | TAACATACTACCCCT[G/T]ATGCAGAGAAATGTG | 166979 |
| rs757184010 | in-del | -/TA | | | intron-variant | CDC20B | GRCh38.p7 | 5:55135235 | GTGTGTGTGTGTCTA[-/TA]TATATATATATATAC | 166979 |
| rs757232939 | snp | G/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55156476 | TGTTCCATTCACTAA[G/T]TCTGTGATCTTGGCT | 166979 |
| rs757269167 | snp | C/T | 1.65302e-05 | 0.00287486 | intron-variant | CDC20B | GRCh38.p7 | 5:55119790 | GGCATTTTACTCACC[C/T]ATTTGCTTACCAAAA | 166979 |
| rs757293056 | snp | A/G/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55165418 | AAATGTAAAAAAGTC[A/G/T]TATAAATTTGTCTAA | 166979 |
| rs757298707 | snp | A/C | 1.65529e-05 | 0.00287683 | missense | CDC20B | GRCh38.p7 | 5:55125017 | TGATAAACACGCCCC[A/C]GTCTTGACCCACTGC | 166979 |
| rs757303168 | snp | A/T | 1.67008e-05 | 0.00288965 | missense | CDC20B | GRCh38.p7 | 5:55128602 | TTCTGAAAACTCCAA[A/T]CTAGGATATTCAGAT | 166979 |
| rs757312632 | snp | C/G | 1.65141e-05 | 0.00287346 | missense | CDC20B | GRCh38.p7 | 5:55128447 | CCTCGCTGGTGCCAA[C/G]TGCCAGGCAAGTTCC | 166979 |
| rs757375986 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55129093 | ATTCTATAGCTTATA[C/T]TAATAAGAAACCTTT | 166979 |
| rs757429256 | snp | C/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55145090 | TTAATTAAGAACCTA[C/G]AAAGTAAAAGGGAGC | 166979 |
| rs757448074 | snp | C/G | 1.81292e-05 | 0.0030107 | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164263 | GAAATGTCTCCATGA[C/G]GGTTTGGTCTCATTT | 166979 |
| rs757504919 | snp | C/G | | | upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55174169 | ATTGGATTGTATTTT[C/G]CTCTAAGGCAATGTG | 166979 |
| rs757634729 | snp | C/T | 3.29468e-05 | 0.00405861 | stop-gained | CDC20B | GRCh38.p7 | 5:55146753 | GTTTGACTTTGCTGC[C/T]ACCTTGTGGTAATGG | 166979 |
| rs757661041 | snp | A/T | 1.64798e-05 | 0.00287047 | missense | CDC20B | GRCh38.p7 | 5:55124877 | GATCGTGGGGCCATA[A/T]TGTCAGCAGTCCATC | 166979 |
| rs757668326 | snp | C/T | 1.64743e-05 | 0.00287 | missense, upstream-variant-2KB | CDC20B, MIR449B, MIR449C | GRCh38.p7 | 5:55172647 | GCACACGCATGATAC[C/T]TTCCTTTGAAAACAC | 166979 |
| rs757686766 | in-del | -/TTTTGT | | | intron-variant | CDC20B | GRCh38.p7 | 5:55146412 | TTAATTTGTCTAAAG[-/TTTTGT]TTTTGTTTTTGTTTT | 166979 |
| rs757705394 | snp | C/G | 3.33361e-05 | 0.00408252 | intron-variant, upstream-variant-2KB | CDC20B, MIR449A, MIR449B, MIR449C | GRCh38.p7 | 5:55172387 | GGCAGAAACTAGAAA[C/G]TACGATTCAGATGCA | 166979 |
| rs757750677 | snp | A/C | 1.67626e-05 | 0.002895 | missense | CDC20B | GRCh38.p7 | 5:55146856 | TAACTGAATCGAGTA[A/C]CTGTTTAACAACAAA | 166979 |
| rs757758349 | in-del | -/CA | | | intron-variant, utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55137176 | AGCGAGACTCTGTCT[-/CA]AAAAAAAAAAAAAAA | 166979 |
| rs757764321 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55122896 | ATGAGTGATCCTGAG[C/T]CAGAACTGCTCAGAT | 166979 |
| rs757794291 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55115809 | AAGAGAGACATATTT[A/G]AGATGCTTATTCTTC | 166979 |
| rs757887560 | in-del | -/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55142675 | CCCGGCCATTCCCTA[-/T]CCCCCAAACCCATAT | 166979 |
| rs757949355 | snp | C/G | 1.64776e-05 | 0.00287028 | missense | CDC20B | GRCh38.p7 | 5:55124964 | CTTGCTTGTGGCGAA[C/G]TGTTCCAACATGATG | 166979 |
| rs758015471 | snp | G/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55146543 | TCAAAGTGACACTCC[G/T]TAGTTCTACAAGACA | 166979 |
| rs758023407 | snp | C/G | | | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160850 | TTACAGTTTTCAATA[C/G]AACTGTGTATGTCCA | 166979 |
| rs758187532 | snp | G/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55127513 | CTGACTGTGTATTAG[G/T]ATCAGCTGGGGAGTC | 166979 |
| rs758243144 | in-del | -/C | 8.34188e-05 | 0.00645774 | utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB | GPX8, CDC20B | GRCh38.p7 | 5:55160148 | CAAGTTTCAGCTCCT[-/C]CTTGAATTCCAGGCT | 166979 |
| rs758254113 | snp | G/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55118950 | TCTCCTCTCACAAAA[G/T]TGTAGGCTCCCTGAG | 166979 |
| rs758257213 | snp | A/G | 1.76275e-05 | 0.00296874 | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164253 | ATAGAACAGAGAAAT[A/G]TCTCCATGAGGGTTT | 166979 |
| rs758258235 | snp | A/G | | | intron-variant, utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55137447 | ATACACAGCATTTGG[A/G]TAACATTTGTCCCCG | 166979 |
| rs758273824 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55132197 | CAATACATTCTCTTG[A/G]AGAAGGAGCTGAAGG | 166979 |
| rs758275498 | snp | G/T | 1.65351e-05 | 0.00287528 | missense, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164092 | GTGGAATTTTTGGAA[G/T]TATCTTGTCAACCCT | 166979 |
| rs758342638 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55165794 | AGGCAAGTCACTTAA[A/G]TACCTTATTTCAGTT | 166979 |
| rs758429390 | in-del | -/C | | | intron-variant, utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55137176 | AGCGAGACTCTGTCT[-/C]AAAAAAAAAAAAAAA | 166979 |
| rs758580617 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55156281 | GGATTATTACAATTC[A/G]AGGTGAGATTTGGGT | 166979 |
| rs758608766 | in-del | -/TTT | | | intron-variant | CDC20B | GRCh38.p7 | 5:55135757 | GAGATTTTTTTGTGA[-/TTT]TTTTTTTTTTTTTTT | 166979 |
| rs758658501 | snp | C/T | 1.65773e-05 | 0.00287895 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55128433 | TACTTGCACTTCTCC[C/T]TCGCTGGTGCCAACT | 166979 |
| rs758714878 | snp | C/G | 4.95405e-05 | 0.00497673 | intron-variant | CDC20B | GRCh38.p7 | 5:55114321 | CTGCCCCTGTGGCCT[C/G]GGGGAAGAAGGAAAG | 166979 |
| rs758719562 | snp | A/G | 1.64768e-05 | 0.00287021 | intron-variant, synonymous-codon | CDC20B | GRCh38.p7 | 5:55120512 | CATTCCTCCTCCAAT[A/G]GCAAGGACCCCAGAC | 166979 |
| rs758788618 | snp | A/C | 1.67539e-05 | 0.00289425 | intron-variant, upstream-variant-2KB, nc-transcript-variant | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170704 | CTGACTTGACCCAAG[A/C]AGCCAGCTAACAATA | 166979 |
| rs758819164 | snp | A/C | 0.000421733 | 0.0145151 | intron-variant, missense | CDC20B | GRCh38.p7 | 5:55137586 | TCAATTAGTCTTTGC[A/C]ACCAACATCCTCCTG | 166979 |
| rs758881272 | snp | A/C | 0.0964597 | 0.197295 | intron-variant, upstream-variant-2KB, nc-transcript-variant | CDC20B, MIR449A, MIR449B, MIR449C | GRCh38.p7 | 5:55172313 | CTGTTAAAATCATTA[A/C]CAGCCGCTAGCAATA | 166979 |
| rs758890805 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55151637 | TAACAATATCCTACC[A/G]CCTTAGCAGGTCTGA | 166979 |
| rs758942409 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55150841 | TCTCGACCTCCCAGA[A/G]CTCAAGCGATCCTCC | 166979 |
| rs758957545 | in-del | -/T | 9.03322e-05 | 0.00671997 | frameshift-variant, upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55172989 | CGCGGTGCGCTCCAG[-/T]TTCCACTCCATCTCC | 166979 |
| rs759074001 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55125176 | TTGGGTTAATAAGGA[C/T]GGAGTGTTCTGCCTG | 166979 |
| rs759092999 | snp | C/T | 1.66305e-05 | 0.00288357 | intron-variant | CDC20B | GRCh38.p7 | 5:55146615 | CGGGGCTGTGGCGTT[C/T]GGGGCACCTCACCTA | 166979 |
| rs759158226 | snp | A/G | | | upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55173549 | ACGGCCCTGATCCCT[A/G]TTCCTCTGCACCCAC | 166979 |
| rs759217079 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55138701 | GATATAGGAGAAGAT[A/G]GTATATCCATGAAGC | 166979 |
| rs759234799 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55169432 | TGACTGGCTGCAAAT[A/G]TCCGCACAAGAATAC | 166979 |
| rs759263896 | snp | C/T | 3.30229e-05 | 0.0040633 | missense, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160194 | TAGAATCCTCCAACA[C/T]GGAGCCTCTTGCAGC | 166979 |
| rs759268346 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55153470 | ACAAATAAGAAAAAT[A/G]CATGCCCCCTGATAG | 166979 |
| rs759309662 | snp | A/T | 1.67136e-05 | 0.00289076 | splice-donor-variant | CDC20B | GRCh38.p7 | 5:55128419 | AAAAAACTGGCCAGT[A/T]CTTGCACTTCTCCCT | 166979 |
| rs759316421 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55149180 | AGCACCACTTCACAC[C/T]CACGAGGATGGCTAG | 166979 |
| rs759353490 | snp | A/G | 1.6495e-05 | 0.0028718 | missense | CDC20B | GRCh38.p7 | 5:55146829 | TGCTCTTAAAGTCAG[A/G]ATACGTAGCATTAAC | 166979 |
| rs759358437 | in-del | -/TTAAAATCA | 0.000287977 | 0.0119961 | intron-variant, upstream-variant-2KB, nc-transcript-variant | CDC20B, MIR449A, MIR449B, MIR449C | GRCh38.p7 | 5:55172301 | TGCAACTAGCAACTG[-/TTAAAATCA]TTAACAGCCGCTAGC | 166979 |
| rs759361609 | snp | A/T | 6.5912e-05 | 0.00574035 | missense | CDC20B | GRCh38.p7 | 5:55119882 | CTTGACCAGTTGCAA[A/T]CTCCTTTGTCTTAGG | 166979 |
| rs759492672 | snp | C/T | | | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160053 | GCTTCATTTCCCCTC[C/T]GAGAAGTGGTCTTTC | 166979 |
| rs759621766 | snp | A/G | 1.64882e-05 | 0.00287121 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55124854 | TTGGCCCTGTGCACT[A/G]GCACCTGGATCGTGG | 166979 |
| rs759693189 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55131302 | TAAAATTACATTGTA[A/C]TCCCTAGAAAAATGA | 166979 |
| rs759741699 | snp | A/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55120211 | CAGTGATGGGGAAAG[A/T]AAGGAAATGTGAAAA | 166979 |
| rs759764855 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55134351 | AAATTCCTGCTTCCG[C/T]GTTAGCTATGAAAAC | 166979 |
| rs759765643 | snp | A/G | 3.30049e-05 | 0.00406219 | synonymous-codon, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55161062 | CTTAGGGCTGAAGGA[A/G]CTGCACAAAGAGTTT | 166979 |
| rs759781630 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55169491 | TGCTACTTCGTGGGT[C/T]AAAATGCCTCCAAGG | 166979 |
| rs759797202 | snp | C/T | 1.64732e-05 | 0.0028699 | missense, upstream-variant-2KB | CDC20B, MIR449B, MIR449C | GRCh38.p7 | 5:55172623 | TCTTCTGCTTCAAGT[C/T]TTTGGAGAGCACACG | 166979 |
| rs759820162 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55150076 | GGCAGAGGTTGCAGT[A/G]AGCCGAGATCGCACC | 166979 |
| rs759881303 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55129660 | AGAAGAGACTCAAAT[C/T]ACCTTAGTAAAGGCT | 166979 |
| rs759889653 | in-del | -/C | 1.65037e-05 | 0.00287256 | frameshift-variant | CDC20B | GRCh38.p7 | 5:55124997 | GGGCTACCCGAACAT[-/C]GTGATGATAAACACG | 166979 |
| rs759891498 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55129112 | TAAGAAACCTTTGAC[C/T]GCTAAGAGAAAACAT | 166979 |
| rs759894199 | snp | A/G | 6.58979e-05 | 0.00573974 | missense | CDC20B | GRCh38.p7 | 5:55124931 | TGCCATCCGGTGACC[A/G]CTTCAGAGCACACAC | 166979 |
| rs759934735 | snp | A/C | | | utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55113536 | TAAGACAATTACAGC[A/C]GACTGGCTGTCAGGC | 166979 |
| rs759936222 | snp | A/G | 1.64811e-05 | 0.00287059 | missense | CDC20B | GRCh38.p7 | 5:55128555 | CCCCATTCCAGATGT[A/G]TACAGCAGAGCCCAG | 166979 |
| rs760100813 | snp | C/G | 1.65833e-05 | 0.00287948 | missense | CDC20B | GRCh38.p7 | 5:55140319 | GATCCTGTACCTTTC[C/G]AAACACATTCGGATT | 166979 |
| rs760168868 | snp | A/G | | | intron-variant, utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55137080 | GTAATCCCAAGCTGA[A/G]ACAGGAGAATCGCTT | 166979 |
| rs760183026 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55115356 | CTTATTTCAGGATTT[A/C]TTCATTTTAGGACTA | 166979 |
| rs760221721 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55151596 | TGTCAGCTATGTCTG[C/T]GAAAACAACATGAGA | 166979 |
| rs760311171 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55134164 | ACTAAGTTCAAACCA[C/T]AGGCCGCTGTCTTTT | 166979 |
| rs760335432 | snp | A/G | 8.2445e-05 | 0.00641995 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55128565 | GATGTATACAGCAGA[A/G]CCCAGGGCTATGGCA | 166979 |
| rs760358901 | snp | A/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55122585 | TGAATGTGGGACTTG[A/T]GACTATCCTGGAACC | 166979 |
| rs760359578 | snp | G/T | 1.68744e-05 | 0.00290463 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164209 | CATAAAAAAGAAAGA[G/T]GATCTATGAGAATGC | 166979 |
| rs760372889 | snp | A/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55166152 | GGGTGTTTTATGCAT[A/T]CACGTTAGGAGCATG | 166979 |
| rs760406195 | snp | C/T | 1.64749e-05 | 0.00287005 | synonymous-codon, upstream-variant-2KB | CDC20B, MIR449A, MIR449B, MIR449C | GRCh38.p7 | 5:55172600 | CACGTTGGCGGAATC[C/T]TGACTTCTCTTCTGC | 166979 |
| rs760427905 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55165005 | AGTCTTTATTTTTGC[A/G]TGAAAATCCCAAGTG | 166979 |
| rs760510360 | snp | A/C | 1.69052e-05 | 0.00290728 | intron-variant | CDC20B | GRCh38.p7 | 5:55128408 | GATGAGAAAAAAAAA[A/C]ACTGGCCAGTACTTG | 166979 |
| rs760596070 | snp | A/C | 1.64789e-05 | 0.0028704 | missense | CDC20B | GRCh38.p7 | 5:55146809 | GGACAGCCTCTTCGC[A/C]AAGTTGCTCTTAAAG | 166979 |
| rs760642006 | snp | C/G | | | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55158835 | CAGCAAAGTTAGGCC[C/G]CCTGTGCCAGGCAAC | 166979 |
| rs760655357 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55118719 | ACCAAAATGGCTCTG[C/T]TAAGAGTTCCCTGTA | 166979 |
| rs760659180 | snp | A/G | | | upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55174345 | TAAGACCCAATCTTA[A/G]ACCAGTTTTCTATGT | 166979 |
| rs760693340 | in-del | -/TATAT | | | intron-variant | CDC20B | GRCh38.p7 | 5:55128849 | TTATTTACACTGAAA[-/TATAT]TTATTTAGAGCCATT | 166979 |
| rs760735062 | snp | A/G | 1.65089e-05 | 0.00287301 | intron-variant | CDC20B | GRCh38.p7 | 5:55127360 | CCCATAACTGAAAAA[A/G]TGAACAAGGAGAGTT | 166979 |
| rs760741866 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55156133 | ATGGCAGCAGGCAAA[A/C]GCTTGTGCTGAAGAA | 166979 |
| rs760750333 | in-del | -/TTTTTTTT | | | intron-variant, upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55172750 | CTTGTCAGATTACAC[-/TTTTTTTT]TTTTTTTTTTTTTTT | 166979 |
| rs760771052 | snp | C/T | 1.73105e-05 | 0.00294193 | intron-variant | CDC20B | GRCh38.p7 | 5:55133566 | CACAGCTCTAAGATC[C/T]TGAAAATATAATATT | 166979 |
| rs760777063 | in-del | -/A | 1.68955e-05 | 0.00290645 | intron-variant | CDC20B | GRCh38.p7 | 5:55125045 | GCGAGTTTACATAAC[-/A]AAAAAAATTAAGCCC | 166979 |
| rs760867018 | snp | A/G | 1.64846e-05 | 0.0028709 | intron-variant | CDC20B | GRCh38.p7 | 5:55120593 | CAGGTCAGCTTCAAA[A/G]GAGGTGCACTCATGA | 166979 |
| rs760878625 | in-del | -/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55135757 | GAGATTTTTTTGTGA[-/T]TTTTTTTTTTTTTTT | 166979 |
| rs760920970 | snp | A/G | 1.64925e-05 | 0.00287158 | stop-gained | CDC20B | GRCh38.p7 | 5:55124847 | TCAGCGGTTGGCCCT[A/G]TGCACTGGCACCTGG | 166979 |
| rs760930685 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55131620 | GCTATAACAATGAGG[A/C]GTTCTTTGGTAATGT | 166979 |
| rs760954118 | in-del | -/C | 5.05131e-05 | 0.00502534 | intron-variant | CDC20B | GRCh38.p7 | 5:55146605 | CGTTGCAAAACGGGG[-/C]TGTGGCGTTTGGGGC | 166979 |
| rs760980468 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55148254 | ATGTTAGCAATAATT[C/T]TTTTGTGACAATCCC | 166979 |
| rs760988846 | snp | C/T | 1.76235e-05 | 0.0029684 | intron-variant | CDC20B | GRCh38.p7 | 5:55125077 | GTTGCTACATAAACA[C/T]TTGAAAACATGGAGG | 166979 |
| rs761041294 | snp | C/T | 1.66349e-05 | 0.00288395 | intron-variant | CDC20B | GRCh38.p7 | 5:55140308 | GACAATGTCTTGATC[C/T]TGTACCTTTCCAAAC | 166979 |
| rs761165116 | snp | A/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55142580 | TCCAATCAGCAGTAG[A/T]GGGTGGAAAACACAG | 166979 |
| rs761184916 | snp | C/T | 2.7598e-05 | 0.0037146 | utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55114179 | ACATCATCATCTTCA[C/T]TCAGAAATAAGGAAA | 166979 |
| rs761199230 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55154989 | GCTATTTCATCTTCA[A/G]TATTTTTAAACTTCT | 166979 |
| rs761331327 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55128231 | AAACTAACCAGAGTA[C/T]CCTTACGTTTTCATT | 166979 |
| rs761384066 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55132118 | TGGGAACAAACATTG[C/T]TTCTTTTTAATATAA | 166979 |
| rs761405796 | in-del | -/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55116478 | TTTGAGACAGGGTCT[-/C]CACTCTGTCACCCAG | 166979 |
| rs761430349 | snp | G/T | 1.64751e-05 | 0.00287007 | missense | CDC20B | GRCh38.p7 | 5:55146696 | TCTGGGAGGTAGGTG[G/T]TTGACTGCTCTTCCC | 166979 |
| rs761455533 | snp | A/C | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164905 | TATAACATTTGAAAA[A/C]GTCTTCATCATTTTC | 166979 |
| rs761461280 | snp | A/G | | | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55161848 | AAGGTCACTTAGCAC[A/G]AAGGTCATGAGGCAT | 166979 |
| rs761478929 | in-del | -/AGA | | | intron-variant | CDC20B | GRCh38.p7 | 5:55125318 | TGGAAAAATAAGCTG[-/AGA]AGATTACCAGATTTT | 166979 |
| rs761510358 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55119486 | CCACCCATTCTACAC[C/T]GCTGGTTTTTCTTCA | 166979 |
| rs761559128 | snp | C/T | 1.648e-05 | 0.0028705 | intron-variant | CDC20B | GRCh38.p7 | 5:55120572 | AGTTTCACATAATAG[C/T]ACAGACAGGTCAGCT | 166979 |
| rs761576655 | snp | A/C | | | intron-variant, upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55172848 | GCTTAGAGTTTCGTA[A/C]CACCTCTTGGTCCTA | 166979 |
| rs761579404 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55123351 | AATTCCCCTGAGCCC[A/G]TGGGCCCCAGTTTTA | 166979 |
| rs761613699 | snp | A/G | 1.87771e-05 | 0.00306401 | intron-variant | CDC20B | GRCh38.p7 | 5:55128396 | CACAGAGAACATGAT[A/G]AGAAAAAAAAAAACT | 166979 |
| rs761653619 | snp | G/T | 4.97236e-05 | 0.00498591 | intron-variant, upstream-variant-2KB, nc-transcript-variant | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170671 | ATCCAGAAGCAAGTG[G/T]CAGGGTAGTTGTGGC | 166979 |
| rs761741915 | snp | C/T | 1.65081e-05 | 0.00287293 | synonymous-codon, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160369 | TGCAAAAGGAAGAAC[C/T]GTTTCTCTGGAAAAG | 166979 |
| rs761786387 | snp | C/T | | | intron-variant, upstream-variant-2KB | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55171640 | CAGGGTCTGGCTCTG[C/T]CCTCCAGGCTGGAGT | 166979 |
| rs761811194 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55151523 | TCTAAACTTTAAATA[C/T]ACATTTTTAAAATTC | 166979 |
| rs761822065 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55152977 | GGCACGGTGGCTCAC[A/G]CTTATAATCCCAGCA | 166979 |
| rs761830830 | in-del | -/TAACTGAATCGAG | 1.65293e-05 | 0.00287479 | frameshift-variant | CDC20B | GRCh38.p7 | 5:55146841 | CAGAATACGTAGCAT[-/TAACTGAATCGAG]TACCTGTTTAACAAC | 166979 |
| rs761879388 | snp | A/G | 1.64882e-05 | 0.00287121 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55146650 | CAAGGTCTCTTTCTC[A/G]GGCGGTGTCTTCAGC | 166979 |
| rs761951181 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55125264 | AAAAATATCCTTTGA[C/T]AGATGTTTCTAATGA | 166979 |
| rs761982699 | snp | C/G | 1.64885e-05 | 0.00287123 | missense, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160227 | ACCCGCTAAAATGTT[C/G]CGGGCCCAGAGCAAA | 166979 |
| rs761988621 | in-del | -/TCGGAG | 1.64866e-05 | 0.00287106 | cds-indel, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55161129 | AATCAGTTTGGAGAA[-/TCGGAG]CCCCGCCCAAGCAAG | 166979 |
| rs761989942 | snp | C/T | 2.68035e-05 | 0.00366074 | utr-variant-5-prime, upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55173029 | CGCCCTGCCTGGCGT[C/T]TGGCCTCTCTGCTCG | 166979 |
| rs761998526 | snp | C/G | 1.64795e-05 | 0.00287045 | intron-variant, missense | CDC20B | GRCh38.p7 | 5:55120459 | GTCTGGATGCTCTTC[C/G]CAGCATTTATATCCA | 166979 |
| rs762005943 | snp | C/T | 5.04783e-05 | 0.0050236 | missense | CDC20B | GRCh38.p7 | 5:55133417 | GATAACTTACAGTAG[C/T]CATTTCGAAGACCAG | 166979 |
| rs762014074 | snp | A/G/T | 3.29545e-05 | 0.00405911 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55124959 | CACAGCTTGCTTGTG[A/G/T]CGAAGTGTTCCAACA | 166979 |
| rs762031715 | in-del | -/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55149293 | GAAAGGATGCAGTCA[-/T]TGTGGAAGATTAGTT | 166979 |
| rs762074841 | snp | C/T | 1.7031e-05 | 0.00291808 | intron-variant | CDC20B | GRCh38.p7 | 5:55133553 | ACAAACACTTCTACA[C/T]AGCTCTAAGATCCTG | 166979 |
| rs762100086 | snp | A/T | | | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55159731 | ACCCATACATGTAAT[A/T]GTAACGTCCTTCAGG | 166979 |
| rs762101309 | snp | C/T | 1.65031e-05 | 0.00287251 | missense | CDC20B | GRCh38.p7 | 5:55143593 | GGAGAGCAGAGTTAC[C/T]TGTTTCAGAAATTCC | 166979 |
| rs762107772 | snp | G/T | 1.68772e-05 | 0.00290488 | intron-variant, downstream-variant-500B | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170523 | ATTCAGTTACACTCT[G/T]ATGTTCATTGTATAT | 166979 |
| rs762171172 | snp | C/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55134102 | TTTACCCATGACTAT[C/G]TAAGGTCAGTATTCT | 166979 |
| rs762186983 | snp | A/T | 0.000103448 | 0.00719121 | intron-variant | CDC20B | GRCh38.p7 | 5:55143462 | CATTTGCAACTAAGT[A/T]GTCTCAGCTTCTCTA | 166979 |
| rs762208074 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55153794 | AAAATTTAATTCAAT[A/C]AAGTTGCATGAACAA | 166979 |
| rs762236820 | snp | G/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55131550 | AGGAGGGATTGATCA[G/T]CTGTCTCAAATATAG | 166979 |
| rs762246876 | snp | G/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55166447 | GTAGGCAGGAGGAGA[G/T]TTGAAAGCGTGTCAT | 166979 |
| rs762286789 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55118555 | TAGCTGAAGGCCATA[C/T]CTAGCTGCTGGAATT | 166979 |
| rs762309290 | snp | A/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55154576 | CAAATATTTAAAGGG[A/T]TGCAATTTATGAATA | 166979 |
| rs762346225 | snp | C/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55167158 | TTTTAACTGTGGTAA[C/G]TAATTCACTGACTTG | 166979 |
| rs762396033 | snp | C/T | 1.69896e-05 | 0.00291454 | intron-variant | CDC20B | GRCh38.p7 | 5:55143656 | ATCCTACAAGAAAGA[C/T]ATTTATCTTTGAATT | 166979 |
| rs762470235 | snp | A/G | 5.04477e-05 | 0.00502208 | intron-variant, upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55172921 | TTAGGGAGAATGCAG[A/G]AAAGGGTGTTACTCA | 166979 |
| rs762490284 | snp | A/G | 1.64852e-05 | 0.00287094 | missense | CDC20B | GRCh38.p7 | 5:55127293 | CAGCTCAGAGCCCCA[A/G]CTACTGACAAATGAC | 166979 |
| rs762512824 | snp | C/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55155822 | TCTGGACCTGCTGCT[C/G]TGCAGACCTCCCGTG | 166979 |
| rs762514200 | snp | A/G | | | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55162352 | GTGAGCTGAAATCGC[A/G]CTACTGCACTCCAGC | 166979 |
| rs762579978 | snp | C/T | 1.65485e-05 | 0.00287645 | intron-variant, upstream-variant-2KB, downstream-variant-500B | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170641 | TCCAGAGCACTTCAT[C/T]GACAAGAAGAATTTA | 166979 |
| rs762644545 | snp | C/G | 0.000273117 | 0.0116826 | stop-lost | CDC20B | GRCh38.p7 | 5:55114218 | TAGAGGGGCTGGGTG[C/G]TAGTAGCAATTCCAT | 166979 |
| rs762664671 | snp | A/T | 1.71681e-05 | 0.00292981 | intron-variant | CDC20B | GRCh38.p7 | 5:55133395 | ACTTTTAATTCCCAA[A/T]CTAAATGATAACTTA | 166979 |
| rs762668784 | snp | A/G | 1.64868e-05 | 0.00287109 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55119909 | TAGGTAGCCAGATTA[A/G]GGAACAAATCTGTAA | 166979 |
| rs762700065 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55134579 | CCCACCTGGGCAACA[C/T]GGTGAAACCCTGTCA | 166979 |
| rs762732428 | snp | A/G | 0.000659304 | 0.0181444 | intron-variant | CDC20B | GRCh38.p7 | 5:55126400 | GCTACTCGGGAGGTG[A/G]AGGTTGCAGTGAGCT | 166979 |
| rs762756335 | snp | A/G | 3.30306e-05 | 0.00406377 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55128580 | GCCCAGGGCTATGGC[A/G]ACAAGATTCTGAAAA | 166979 |
| rs762798027 | snp | A/G | | | intron-variant, utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55136701 | GAACTTATTCCAGAG[A/G]GGAAATGTAGCAGGC | 166979 |
| rs762826823 | snp | C/G | 1.64905e-05 | 0.00287141 | missense, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160346 | TTTTATGCCTTTGAA[C/G]TGAAGGATGCAAAAG | 166979 |
| rs762885626 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55149361 | ATGACCAAGCAAGTC[C/T]ACTCATAGGTATATG | 166979 |
| rs762888009 | snp | G/T | | | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55163634 | GTCTCAGCCTCCCGA[G/T]TAGCTGGGATTACAG | 166979 |
| rs762915719 | snp | C/T | | | utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55113244 | CAAAAGACAGAACAG[C/T]GAACTGATCAAGTTT | 166979 |
| rs762997813 | snp | C/G | | | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55158428 | TACTTTCTGCATAAT[C/G]ATTGCTTTTTCTACT | 166979 |
| rs763018979 | in-del | -/T | 1.69003e-05 | 0.00290687 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55161265 | TTGTTGGTAAATATC[-/T]GCCTTGCATATGCTG | 166979 |
| rs763120289 | snp | C/G | 1.6492e-05 | 0.00287154 | missense, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160215 | CTCTTGCAGCTTACC[C/G]GCTAAAATGTTCCGG | 166979 |
| rs763128998 | snp | C/T | 1.64735e-05 | 0.00286993 | synonymous-codon, upstream-variant-2KB | CDC20B, MIR449B, MIR449C | GRCh38.p7 | 5:55172633 | CAAGTCTTTGGAGAG[C/T]ACACGCATGATACTT | 166979 |
| rs763165516 | snp | G/T | 1.6543e-05 | 0.00287597 | missense | CDC20B | GRCh38.p7 | 5:55140334 | CAAACACATTCGGAT[G/T]GCTCACAGAGCTGCA | 166979 |
| rs763170063 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55121726 | GGCTAAAGGTTACAT[A/G]AAGTTAAAAATGTTA | 166979 |
| rs763202338 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55157148 | TCCTCCTATAGAAGC[C/T]TTCCTTCATTTACTG | 166979 |
| rs763233068 | snp | A/G | | | intron-variant, upstream-variant-2KB | CDC20B, MIR449A, MIR449B, MIR449C | GRCh38.p7 | 5:55172560 | GATCAGAATTAAAAC[A/G]GAGAACAAGAACAAG | 166979 |
| rs763243171 | snp | C/T | 3.30175e-05 | 0.00406296 | synonymous-codon, intron-variant, utr-variant-3-prime, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164164 | TGAAGTCATCAGGCC[C/T]GACATAGCAGCTCTG | 166979 |
| rs763275737 | snp | A/G | 0.000119402 | 0.00772572 | intron-variant | CDC20B | GRCh38.p7 | 5:55133403 | TTCCCAATCTAAATG[A/G]TAACTTACAGTAGTC | 166979 |
| rs763290354 | snp | A/G | | | intron-variant, upstream-variant-2KB | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55171440 | ACATAAGCTGTGCAC[A/G]ACACAAAACTGCAGC | 166979 |
| rs763304852 | snp | A/G | | | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55161534 | AGTGTGCCCATGGCT[A/G]TTTTCACAAAATATC | 166979 |
| rs763305642 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55116743 | GCCTTCACTCTTTTG[C/T]GTTATGATGAAGAAG | 166979 |
| rs763334371 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55131484 | AAAAGGATGAGAAAG[A/C]GTGAACAAAAGACAC | 166979 |
| rs763345685 | snp | A/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55165341 | CAAGTTGGTGAAGGT[A/T]AATTATTGCCTCATG | 166979 |
| rs763357050 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55115693 | GCTCAAAGGACCAGT[A/G]CTGCCTACGACTCAA | 166979 |
| rs763387665 | snp | C/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55129258 | TAAACCCCTACAATA[C/G]ATTCCGTCCCCATGA | 166979 |
| rs763435648 | snp | A/G | 3.29652e-05 | 0.00405974 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55124866 | ACTGGCACCTGGATC[A/G]TGGGGCCATATTGTC | 166979 |
| rs763490469 | snp | C/T | 1.64754e-05 | 0.00287009 | missense | CDC20B | GRCh38.p7 | 5:55124946 | ACTTCAGAGCACACA[C/T]AGCTTGCTTGTGGCG | 166979 |
| rs763603995 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55116551 | CCTCCTGGACTCAAG[C/T]GATCCTTCCACCTCA | 166979 |
| rs763661880 | snp | A/C | | | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55162359 | GAAATCGCGCTACTG[A/C]ACTCCAGCCTGGGCG | 166979 |
| rs763702502 | in-del | -/TG | | | intron-variant | CDC20B | GRCh38.p7 | 5:55135219 | ATAATAAAGTGTATG[-/TG]TGTGTGTGTGTGTCT | 166979 |
| rs763715326 | snp | A/G | 3.30715e-05 | 0.00406628 | missense | CDC20B | GRCh38.p7 | 5:55125012 | CGTGATGATAAACAC[A/G]CCCCAGTCTTGACCC | 166979 |
| rs763752758 | snp | A/T | 1.64923e-05 | 0.00287156 | stop-gained | CDC20B | GRCh38.p7 | 5:55146646 | GAGTCAAGGTCTCTT[A/T]CTCAGGCGGTGTCTT | 166979 |
| rs763785673 | in-del | -/AG | | | intron-variant | CDC20B | GRCh38.p7 | 5:55124699 | GCAAATTCTAGAGAA[-/AG]AAAAATCTCAAAATA | 166979 |
| rs763833126 | snp | G/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55126553 | AATATGAAAATGAAT[G/T]GCTATGATTAAAAGC | 166979 |
| rs763937570 | snp | A/G | | | intron-variant, upstream-variant-2KB | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55171586 | TGTATTCAATATAGG[A/G]TGTTACCACTTGAAT | 166979 |
| rs763991710 | snp | A/T | | | upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55174330 | AAATGGCATTAGAAC[A/T]AAGACCCAATCTTAG | 166979 |
| rs764016237 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55134593 | ACGGTGAAACCCTGT[C/T]ACTACAAAAAATGCA | 166979 |
| rs764044632 | in-del | -/AATTACAGATTC | | | intron-variant, downstream-variant-500B | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170500 | ACATAAACACACACT[-/AATTACAGATTC]AGTTACACTCTGATG | 166979 |
| rs764053742 | snp | A/T | 1.65512e-05 | 0.00287669 | intron-variant, upstream-variant-2KB, nc-transcript-variant | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170646 | AGCACTTCATTGACA[A/T]GAAGAATTTATCCAG | 166979 |
| rs764073084 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55150184 | TTTAAATATGTGCAT[C/T]TCACTTCAATAAAAG | 166979 |
| rs764144733 | snp | C/T | 1.65124e-05 | 0.00287331 | missense | CDC20B | GRCh38.p7 | 5:55146835 | TAAAGTCAGAATACG[C/T]AGCATTAACTGAATC | 166979 |
| rs764145740 | snp | C/T | 0.000148996 | 0.00862992 | intron-variant, nc-transcript-variant, downstream-variant-500B | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170566 | CAGTTGCATGTTAGC[C/T]GATGCCATTCACATA | 166979 |
| rs764212280 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55144369 | CTGGAAACCTGTCAA[A/G]TCATTCTCTAAAACT | 166979 |
| rs764216767 | in-del | -/A/AA/AAA | | | intron-variant | CDC20B | GRCh38.p7 | 5:55126466 | GTGAGATTCCATGTC[-/A/AA/AAA]AAAAAAAAAAAAAAA | 166979 |
| rs764233309 | in-del | -/C | 1.64796e-05 | 0.00287046 | frameshift-variant | CDC20B | GRCh38.p7 | 5:55146672 | GTCTTCAGCACTGAT[-/C]CGGAAGCTTCTGGGA | 166979 |
| rs764277291 | snp | A/G | 1.65004e-05 | 0.00287227 | intron-variant, upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55172919 | AGTTAGGGAGAATGC[A/G]GAAAAGGGTGTTACT | 166979 |
| rs764297435 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55120671 | ACAGCTCTCCTGGGC[C/T]TGCTATCTAAAGGCA | 166979 |
| rs764455563 | snp | C/T | 3.29538e-05 | 0.00405904 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55124953 | AGCACACACAGCTTG[C/T]TTGTGGCGAAGTGTT | 166979 |
| rs764456794 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55157161 | GCCTTCCTTCATTTA[C/T]TGAAAGAGCGCTGGT | 166979 |
| rs764463657 | snp | C/G/T | 3.29474e-05 | 0.00405867 | missense, upstream-variant-2KB | CDC20B, MIR449B, MIR449C | GRCh38.p7 | 5:55172637 | TCTTTGGAGAGCACA[C/G/T]GCATGATACTTTCCT | 166979 |
| rs764485437 | snp | A/G | 1.64819e-05 | 0.00287066 | missense | CDC20B | GRCh38.p7 | 5:55124868 | TGGCACCTGGATCGT[A/G]GGGCCATATTGTCAG | 166979 |
| rs764535391 | snp | A/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55129259 | AAACCCCTACAATAC[A/T]TTCCGTCCCCATGAT | 166979 |
| rs764556076 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55115694 | CTCAAAGGACCAGTA[C/T]TGCCTACGACTCAAT | 166979 |
| rs764567107 | snp | A/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55151731 | CCCCAGTTTTCTGCC[A/T]GGGTAAATCCCAGCC | 166979 |
| rs764573585 | snp | C/T | 3.30781e-05 | 0.00406669 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55140336 | AACACATTCGGATTG[C/T]TCACAGAGCTGCATT | 166979 |
| rs764594607 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55125276 | TGATAGATGTTTCTA[A/C]TGACTTTAATCTGAT | 166979 |
| rs764607524 | snp | A/C | | | utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55113714 | GATTTTTAGAGAGAG[A/C]AATATGCATGCTTAA | 166979 |
| rs764625402 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55143647 | CTTTGCGGGATCCTA[C/T]AAGAAAGACATTTAT | 166979 |
| rs764686625 | snp | G/T | 4.98699e-05 | 0.00499324 | missense, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160392 | TGGAAAAGTATAAAG[G/T]CAAAGTAAGTTGCAT | 166979 |
| rs764687096 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55130415 | TAACATATGTGTAAG[C/T]AGAGTCAGGTCTTAG | 166979 |
| rs764695296 | snp | A/T | | | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55161658 | GTTAACATATGTTTG[A/T]GGCTAATTTTATGTT | 166979 |
| rs764719662 | snp | C/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55165371 | GAAATATACATTCAT[C/G]GCATAAAAGAATTAA | 166979 |
| rs764747365 | snp | A/G | 2.73437e-05 | 0.00369745 | missense, upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55172945 | TTACTCACCCACAGC[A/G]TCTCCTCTTCCGTGC | 166979 |
| rs764821924 | snp | C/T | 1.65288e-05 | 0.00287474 | missense | CDC20B | GRCh38.p7 | 5:55125009 | CATCGTGATGATAAA[C/T]ACGCCCCAGTCTTGA | 166979 |
| rs764902001 | snp | C/T | 1.6649e-05 | 0.00288518 | intron-variant, nc-transcript-variant, downstream-variant-500B | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170538 | GATGTTCATTGTATA[C/T]GCAATAAGACAGCAG | 166979 |
| rs764937355 | snp | C/G | 1.66527e-05 | 0.00288549 | intron-variant | CDC20B | GRCh38.p7 | 5:55119763 | CAACAGCTCACTTTG[C/G]TATAGGTGCATGGCA | 166979 |
| rs764938353 | snp | A/G | | | upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55174024 | GGCTGTGCAGCCTTA[A/G]CTGCCCATCTGAGCT | 166979 |
| rs764970678 | snp | A/C | | | intron-variant, utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55137270 | AGGCAATTATCTCCC[A/C]ACTGCATGGCTACAG | 166979 |
| rs765016309 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55133220 | CCACACCATGCCAAC[A/G]TTAACAATACCATCC | 166979 |
| rs765031404 | snp | A/C | 1.66048e-05 | 0.00288134 | stop-gained | CDC20B | GRCh38.p7 | 5:55128429 | CCAGTACTTGCACTT[A/C]TCCCTCGCTGGTGCC | 166979 |
| rs765032731 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55138924 | GTCAATCCAGGATAT[C/T]TCATAAAGAAGGAAA | 166979 |
| rs765052774 | snp | G/T | | | intron-variant, downstream-variant-500B | GPX8, CDC20B | GRCh38.p7 | 5:55167724 | AAAAATTAGCTGGGT[G/T]TAGTGGCACATGCCT | 166979 |
| rs765074632 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55132063 | GACTCTGTTTAAAAA[A/G]AAAGAAAGAAAGAAA | 166979 |
| rs765099025 | in-del | -/AGTTAT | 1.65272e-05 | 0.0028746 | intron-variant | CDC20B | GRCh38.p7 | 5:55127372 | AAAATGAACAAGGAG[-/AGTTAT]GTAGCATTGGAGTTT | 166979 |
| rs765126958 | in-del | -/TT | | | intron-variant | CDC20B | GRCh38.p7 | 5:55135758 | AGATTTTTTTGTGAT[-/TT]TTTTTTTTTTTTTTT | 166979 |
| rs765128107 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55148605 | TGTAGTCCTAGCTAC[C/T]TGATGGGGCTGAGGC | 166979 |
| rs765171520 | snp | C/G | 8.24151e-05 | 0.00641878 | missense | CDC20B | GRCh38.p7 | 5:55119901 | CTTTGTCTTAGGTAG[C/G]CAGATTAAGGAACAA | 166979 |
| rs765188566 | in-del | -/TCCAC | 1.76855e-05 | 0.00297362 | intron-variant | CDC20B | GRCh38.p7 | 5:55146884 | AAAAACAGCTGTAAG[-/TCCAC]TGGCCTCAGTGATGC | 166979 |
| rs765210068 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55149229 | TAATAAGCATTGGTA[A/C]GGATGCGAAGAAACT | 166979 |
| rs765246334 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55156196 | ACTTATTCACTACCA[C/T]AAGAACAGTATAGGG | 166979 |
| rs765260206 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55142903 | CGAACTGAAATATGG[A/G]TTCCTTCAAAGACTC | 166979 |
| rs765265979 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55123457 | TATAATAAATATTTT[A/G]GCAAAACTAGAAGCT | 166979 |
| rs765282720 | snp | C/T | 1.64738e-05 | 0.00286995 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55146734 | ATCAGAGGACAGAGC[C/T]CTAGTTTGACTTTGC | 166979 |
| rs765341061 | snp | C/G | 3.29468e-05 | 0.00405861 | missense, upstream-variant-2KB | CDC20B, MIR449B, MIR449C | GRCh38.p7 | 5:55172628 | TGCTTCAAGTCTTTG[C/G]AGAGCACACGCATGA | 166979 |
| rs765418729 | snp | C/G | 4.94572e-05 | 0.00497254 | missense | CDC20B | GRCh38.p7 | 5:55124859 | CCTGTGCACTGGCAC[C/G]TGGATCGTGGGGCCA | 166979 |
| rs765526056 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55120311 | TGAGAACTCAAATTC[C/T]TTATGGACTCAATAG | 166979 |
| rs765619994 | snp | A/G | 1.65616e-05 | 0.00287759 | missense | CDC20B | GRCh38.p7 | 5:55140326 | TACCTTTCCAAACAC[A/G]TTCGGATTGCTCACA | 166979 |
| rs765651143 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55129187 | TCAGTCAGAAACTCC[C/T]GACTGACACGTATCA | 166979 |
| rs765695124 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55161068 | GCTGAAGGAACTGCA[C/T]AAAGAGTTTGGACCA | 166979 |
| rs765704325 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55125926 | TTGAGGATAAGAGAC[C/T]ACCTTATCATGTTAC | 166979 |
| rs765711152 | snp | G/T | | | missense, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164077 | AAAGAAGGAACCAAG[G/T]TGGAATTTTTGGAAG | 166979 |
| rs765782216 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55144198 | TCTCTCCCCCTTTCT[A/G]TTGCAGAAAGATGTT | 166979 |
| rs765785450 | snp | A/T | 5.09411e-05 | 0.00504658 | stop-lost, intron-variant, utr-variant-3-prime, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164218 | GAAAGAGGATCTATG[A/T]GAATGCCATTGCGTT | 166979 |
| rs765803355 | in-del | -/TCT | | | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55159020 | TTTTGCTTTTTTCCC[-/TCT]TCTTCTTTTGTTCTG | 166979 |
| rs765846305 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55122544 | CATTCCCTCCATCAA[C/T]AGGTACAATCTAATT | 166979 |
| rs765851467 | snp | A/G | 4.9597e-05 | 0.00497956 | missense | CDC20B | GRCh38.p7 | 5:55140370 | CCATTAGCCTGCTGA[A/G]CCACGTTCTGGGTTA | 166979 |
| rs765901426 | in-del | -/AAAG | | | intron-variant | CDC20B | GRCh38.p7 | 5:55129570 | GACATGGGAAAGCCA[-/AAAG]AAAGAGATCCTCTGA | 166979 |
| rs765976968 | snp | C/G | 1.72484e-05 | 0.00293665 | intron-variant | CDC20B | GRCh38.p7 | 5:55143470 | ACTAAGTTGTCTCAG[C/G]TTCTCTAGATGTGGG | 166979 |
| rs765981639 | snp | A/G | 3.46687e-05 | 0.00416331 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164044 | ATGAAAATATGTTCT[A/G]GATATTTTAGATTCT | 166979 |
| rs765994754 | snp | A/G | 6.64066e-05 | 0.00576185 | intron-variant | CDC20B | GRCh38.p7 | 5:55114364 | CCTCCACGTTACATG[A/G]GCTGCTGCTCAGGAC | 166979 |
| rs766039569 | snp | C/T | | | intron-variant, utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55137091 | CTGAGACAGGAGAAT[C/T]GCTTGAACCCGGGAG | 166979 |
| rs766059677 | snp | A/G | 1.65293e-05 | 0.00287479 | intron-variant | CDC20B | GRCh38.p7 | 5:55127373 | AAATGAACAAGGAGA[A/G]TTATGTAGCATTGGA | 166979 |
| rs766076353 | snp | C/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55165234 | GTAGATCAGCAGTCA[C/G]TGAACCTCTTAGAGT | 166979 |
| rs766100242 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55146285 | CTGTAGCCAATCAGG[C/T]CGGCTCCTACGCACT | 166979 |
| rs766116436 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55153425 | CACTTTCAGAACCAA[C/T]ACTTGTTAGTGATCT | 166979 |
| rs766147454 | snp | A/G | 1.64749e-05 | 0.00287005 | missense | CDC20B | GRCh38.p7 | 5:55146714 | GACTGCTCTTCCCCA[A/G]AGGAATCAGAGGACA | 166979 |
| rs766156161 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55148276 | GACAATCCCTGGTGT[C/T]GAAGGTGCCAAAAAC | 166979 |
| rs766166053 | in-del | -/A | 1.79451e-05 | 0.00299537 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164010 | AGTGAAAATCTTGAC[-/A]AAGAATAAAATTATG | 166979 |
| rs766167696 | snp | G/T | 1.64803e-05 | 0.00287052 | missense | CDC20B | GRCh38.p7 | 5:55146815 | CCTCTTCGCAAAGTT[G/T]CTCTTAAAGTCAGAA | 166979 |
| rs766174392 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55151608 | CTGCGAAAACAACAT[A/G]AGAAGTTGCACGTTA | 166979 |
| rs766201855 | snp | A/G | | | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55159840 | AAACAGTTGCTCAAT[A/G]AATACACAGCTTAGC | 166979 |
| rs766258930 | in-del | -/A | 3.30273e-05 | 0.00406356 | frameshift-variant, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160193 | CTAGAATCCTCCAAC[-/A]TGGAGCCTCTTGCAG | 166979 |
| rs766295555 | snp | A/G | 1.68439e-05 | 0.00290201 | intron-variant | CDC20B | GRCh38.p7 | 5:55128412 | AGAAAAAAAAAAACT[A/G]GCCAGTACTTGCACT | 166979 |
| rs766373291 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55117682 | GCAGTGCTCCCTCAG[C/T]GTGTTCATGGAACAA | 166979 |
| rs766386686 | snp | A/C | 3.29554e-05 | 0.00405914 | intron-variant, missense | CDC20B | GRCh38.p7 | 5:55120491 | GATGTGTAAGCGTCC[A/C]TCCTTCATTCCTCCT | 166979 |
| rs766394338 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55155044 | GGAAATGCCTGTCGC[A/G]TAGTTTTGAATGACT | 166979 |
| rs766463626 | snp | A/G | | | intron-variant, downstream-variant-500B | GPX8, CDC20B | GRCh38.p7 | 5:55167367 | CAATAGTATATATAC[A/G]TGTACATATATATAA | 166979 |
| rs766477340 | snp | A/G | 1.64846e-05 | 0.0028709 | intron-variant | CDC20B | GRCh38.p7 | 5:55120597 | TCAGCTTCAAAGGAG[A/G]TGCACTCATGAATGT | 166979 |
| rs766506616 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55118778 | CTGAAGAATACAAAG[A/G]TCATTCTGAGGCTGA | 166979 |
| rs766581406 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55126792 | GCTCTCCAGGTGATT[A/C]TGATACATGTTCTAG | 166979 |
| rs766584251 | snp | C/T | 5.28016e-05 | 0.0051379 | intron-variant | CDC20B | GRCh38.p7 | 5:55133580 | CCTGAAAATATAATA[C/T]TTATTCTTGTGGGAA | 166979 |
| rs766602349 | snp | G/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55128889 | AACTTGGCAGATTCA[G/T]CTACCATTATTAGTA | 166979 |
| rs766658493 | snp | A/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55166533 | TTAGGCTATGTGTGC[A/T]GAGAGAGGGAGCGGA | 166979 |
| rs766772004 | snp | C/T | 0.000246457 | 0.0110981 | intron-variant | CDC20B | GRCh38.p7 | 5:55126335 | GAAACCCCATCTCTA[C/T]TAAAAATACAAAAAT | 166979 |
| rs766781773 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55142748 | CACTTCCAATTGCAT[A/G]TGAGTTCAGATAACT | 166979 |
| rs766823236 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55123904 | TACAATGTAGTGGCA[A/G]CAGTCACTATATATT | 166979 |
| rs766953333 | snp | A/G | 1.66211e-05 | 0.00288275 | missense | CDC20B | GRCh38.p7 | 5:55133432 | TCATTTCGAAGACCA[A/G]TAATATGAATCTTCA | 166979 |
| rs766955472 | snp | C/G | 3.30267e-05 | 0.00406353 | synonymous-codon, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55161053 | CAGAAATTACTTAGG[C/G]CTGAAGGAACTGCAC | 166979 |
| rs766957067 | in-del | -/A | | | intron-variant | CDC20B | GRCh38.p7 | 5:55128262 | AAAAACCATTCAGTA[-/A]AAAAAAAAAAAAAAA | 166979 |
| rs766971015 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55135041 | TGTAAACTATGGACT[C/T]TTGGTGACCATGATG | 166979 |
| rs767064340 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55150295 | AGGGACTATAAAAGA[A/G]TATTCCAATACAGTC | 166979 |
| rs767127067 | snp | A/C/G | 3.29757e-05 | 0.00406041 | missense, stop-gained | CDC20B | GRCh38.p7 | 5:55114277 | AAAACACCCGGGTCT[A/C/G]GTCTGGACTCAAAGA | 166979 |
| rs767162488 | snp | A/G | | | utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55113454 | GATGAGCAGGGGACT[A/G]AGAGGATCAGCACAG | 166979 |
| rs767177389 | snp | C/T | 1.64895e-05 | 0.00287132 | missense, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55161087 | GAGTTTGGACCATCC[C/T]ACTTCAGCGTGTTGG | 166979 |
| rs767219704 | snp | A/G | | | synonymous-codon | CDC20B | GRCh38.p7 | 5:55128439 | CACTTCTCCCTCGCT[A/G]GTGCCAACTGCCAGG | 166979 |
| rs767262389 | snp | C/T | | | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55163798 | CAGACTGAGCCACGG[C/T]TCCCAGCCTACTTTG | 166979 |
| rs767281196 | snp | A/T | 1.65789e-05 | 0.0028791 | intron-variant, upstream-variant-2KB, nc-transcript-variant | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170673 | CCAGAAGCAAGTGGC[A/T]GGGTAGTTGTGGCTG | 166979 |
| rs767311182 | in-del | -/A | 3.29459e-05 | 0.00405856 | splice-donor-variant, upstream-variant-2KB | CDC20B, MIR449A, MIR449B, MIR449C | GRCh38.p7 | 5:55172585 | ACAAGCCCTGGACTC[-/A]ACGTTGGCGGAATCT | 166979 |
| rs767348589 | in-del | -/TC | | | intron-variant | CDC20B | GRCh38.p7 | 5:55116154 | ACCCTGATGAAAGAA[-/TC]TCTTTTTTTTATGGA | 166979 |
| rs767360723 | snp | A/G | | | intron-variant, upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55172869 | CTTGGTCCTAAACAG[A/G]TATTATGAACGGGGC | 166979 |
| rs767365746 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55117275 | CCAAAAAAAATCATG[A/C]CTATGGTTAACAGGG | 166979 |
| rs767396983 | snp | C/T | 1.64857e-05 | 0.00287099 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55146653 | GGTCTCTTTCTCAGG[C/T]GGTGTCTTCAGCACT | 166979 |
| rs767410087 | snp | A/T | | | intron-variant, upstream-variant-2KB, downstream-variant-500B | CDC20B, MIR449A, MIR449B, MIR449C | GRCh38.p7 | 5:55171788 | TTGCAGTTTTTTTAT[A/T]AAGACAAGGTCTCCC | 166979 |
| rs767418788 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55114772 | CTCCTCTTCTGTGTG[C/T]CTTTTCTCCTCTGTG | 166979 |
| rs767420739 | in-del | -/A | | | intron-variant | CDC20B | GRCh38.p7 | 5:55143169 | TCATCAAATAGTTGG[-/A]AATGATGACAGCAAG | 166979 |
| rs767428387 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55115896 | CACACACACACACGC[A/G]CACACACACCACACA | 166979 |
| rs767437309 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55122292 | TTTTTTTTTTTAAGA[C/T]ACAGTCTCACTCTGT | 166979 |
| rs767488282 | snp | C/T | | | intron-variant, utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55137066 | GGTGGTGTGTGCCTG[C/T]AATCCCAAGCTGAGA | 166979 |
| rs767541344 | snp | A/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55166459 | AGATTTGAAAGCGTG[A/T]CATACATATTGCCTT | 166979 |
| rs767563005 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55131570 | CTCAAATATAGTTGT[C/T]AGGGTTCGGTATGAA | 166979 |
| rs767601572 | snp | C/T | 1.67705e-05 | 0.00289568 | missense | CDC20B | GRCh38.p7 | 5:55133420 | AACTTACAGTAGTCA[C/T]TTCGAAGACCAGTAA | 166979 |
| rs767618441 | snp | A/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55130453 | ATAACAAGGTGACCA[A/T]GGGGTTCTCACCAGA | 166979 |
| rs767657385 | in-del | -/GA | 1.65149e-05 | 0.00287353 | frameshift-variant | CDC20B | GRCh38.p7 | 5:55125003 | CCCGAACATCGTGAT[-/GA]TAAACACGCCCCAGT | 166979 |
| rs767667527 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55149413 | GCACATATGTTCATA[A/G]TAGCACTAATCACAA | 166979 |
| rs767726535 | snp | C/T | 1.6477e-05 | 0.00287024 | intron-variant, missense | CDC20B | GRCh38.p7 | 5:55120478 | CATTTATATCCAAGA[C/T]GTGTAAGCGTCCATC | 166979 |
| rs767762834 | snp | G/T | 1.65119e-05 | 0.00287327 | missense, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160371 | CAAAAGGAAGAACTG[G/T]TTCTCTGGAAAAGTA | 166979 |
| rs767836865 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55148120 | AAGTTTACCAACTCA[A/G]CAGAAAAACTGGGCC | 166979 |
| rs767867102 | snp | A/T | 1.65108e-05 | 0.00287317 | missense | CDC20B | GRCh38.p7 | 5:55125001 | TACCCGAACATCGTG[A/T]TGATAAACACGCCCC | 166979 |
| rs767883088 | snp | A/G | 4.95193e-05 | 0.00497566 | missense | CDC20B | GRCh38.p7 | 5:55143619 | ATTCCTTTGCTGGGG[A/G]TCTTCAGTTGTTCTT | 166979 |
| rs767901303 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55154785 | TTAATGTCATTTTAT[A/G]ATTTTTCAGGTTTGA | 166979 |
| rs768057268 | snp | A/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55167169 | GTAACTAATTCACTG[A/T]CTTGAAGTTTGCTTT | 166979 |
| rs768057975 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55139332 | GAGCACAACATAGCT[A/G]CCCAAAAATAGTGGA | 166979 |
| rs768067909 | snp | C/T | 1.64882e-05 | 0.00287121 | synonymous-codon, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160228 | CCCGCTAAAATGTTC[C/T]GGGCCCAGAGCAAAG | 166979 |
| rs768090791 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55117070 | CAACTATAGTCATAA[A/G]TGAGACCACATATTG | 166979 |
| rs768098392 | snp | C/T | 3.15075e-05 | 0.00396897 | utr-variant-5-prime, upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55173046 | GGCCTCTCTGCTCGA[C/T]TGCCTCTGGTTTTCT | 166979 |
| rs768153512 | snp | A/G | 4.57112e-05 | 0.00478053 | intron-variant, upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55172926 | GAGAATGCAGAAAAG[A/G]GTGTTACTCACCCAC | 166979 |
| rs768183598 | snp | C/T | 1.65217e-05 | 0.00287412 | missense | CDC20B | GRCh38.p7 | 5:55124826 | CCGTAGACTGGGTTA[C/T]GACTTTCAGCGGTTG | 166979 |
| rs768187162 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55144007 | TGGAAAAAAAAAAAA[A/C]AAAACCAGATTTGCA | 166979 |
| rs768223172 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55128087 | CTGTACTCTTAATCA[C/T]GGCTTCAGGTGAAAA | 166979 |
| rs768245876 | snp | A/G | 1.64776e-05 | 0.00287028 | missense | CDC20B | GRCh38.p7 | 5:55146688 | CGGAAGCTTCTGGGA[A/G]GTAGGTGGTTGACTG | 166979 |
| rs768247877 | snp | A/T | 1.64741e-05 | 0.00286998 | intron-variant, upstream-variant-2KB | CDC20B, MIR449A, MIR449B, MIR449C | GRCh38.p7 | 5:55172571 | AAACAGAGAACAAGA[A/T]CAAGCCCTGGACTCA | 166979 |
| rs768305495 | snp | C/T | 1.64836e-05 | 0.0028708 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55127298 | CAGAGCCCCAACTAC[C/T]GACAAATGACCAAGC | 166979 |
| rs768325446 | in-del | -/A | 1.64827e-05 | 0.00287073 | intron-variant | CDC20B | GRCh38.p7 | 5:55120392 | AGATTCCAGAAGATC[-/A]AAATGAAGATGAAGC | 166979 |
| rs768337473 | snp | A/T | 2.06627e-05 | 0.00321417 | intron-variant, upstream-variant-2KB | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170766 | TCTCGTGGCCCAGGC[A/T]GTCACTGAGGCTAAA | 166979 |
| rs768369921 | snp | A/G | | | intron-variant, utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55136727 | CAGGCAAGTTTCCTT[A/G]GCATTTATGAAATGA | 166979 |
| rs768374230 | snp | A/G | 1.64743e-05 | 0.00287 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55146767 | CCACCTTGTGGTAAT[A/G]GGGCTACTCGCAACA | 166979 |
| rs768433411 | snp | A/C | 8.43206e-05 | 0.00649255 | intron-variant | CDC20B | GRCh38.p7 | 5:55133540 | CAGCCTACAAGAAAC[A/C]AACACTTCTACACAG | 166979 |
| rs768441225 | snp | A/G | | | upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55173861 | AGAGGTGAAGAGGTA[A/G]TGAAAGAACCAGTGA | 166979 |
| rs768508311 | snp | A/G | 1.6832e-05 | 0.00290099 | missense, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160994 | TTCTTTTTCCGGGAG[A/G]TTTCACTAGTTGTAA | 166979 |
| rs768562690 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55151499 | CTTAGAGCAAAATTC[A/C]AAAGAAATTCTAAAC | 166979 |
| rs768627685 | snp | A/C | 4.94311e-05 | 0.00497123 | intron-variant, missense | CDC20B | GRCh38.p7 | 5:55120550 | GACACCAATCCATGG[A/C]CTTTAAAGTTTCACA | 166979 |
| rs768691711 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164858 | ATGTATGTAACTGAC[A/G]TATATAAATAGTCAT | 166979 |
| rs768719001 | snp | A/G | 1.6492e-05 | 0.00287154 | missense, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160352 | GCCTTTGAAGTGAAG[A/G]ATGCAAAAGGAAGAA | 166979 |
| rs768743886 | snp | A/G | | | utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55113245 | AAAAGACAGAACAGC[A/G]AACTGATCAAGTTTG | 166979 |
| rs768794706 | snp | A/T | | | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55159576 | TCTTTTAACACCTTC[A/T]CTGTTTTTAACATAT | 166979 |
| rs768887293 | in-del | -/AAAG | 1.64974e-05 | 0.00287201 | frameshift-variant, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55161069 | CTGAAGGAACTGCAC[-/AAAG]AGTTTGGACCATCCC | 166979 |
| rs768977229 | snp | C/T | 1.69355e-05 | 0.00290989 | intron-variant, downstream-variant-500B | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170521 | AGATTCAGTTACACT[C/T]TGATGTTCATTGTAT | 166979 |
| rs768993028 | snp | C/G | | | upstream-variant-2KB | CDC20B | GRCh38.p7 | 5:55174918 | CCCTAGTGTGAAGTA[C/G]AGAAAGTATTAGTCA | 166979 |
| rs768993047 | snp | C/T | | | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55158433 | TCTGCATAATCATTG[C/T]TTTTTCTACTGTATC | 166979 |
| rs769004347 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55132803 | ATTGCCATTAAATAT[C/T]TTAATTACCAACATC | 166979 |
| rs769015171 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55131482 | AAAAAAGGATGAGAA[A/G]GAGTGAACAAAAGAC | 166979 |
| rs769044384 | snp | C/T | | | intron-variant, upstream-variant-2KB | CDC20B, MIR449A, MIR449B, MIR449C | GRCh38.p7 | 5:55172572 | AACAGAGAACAAGAA[C/T]AAGCCCTGGACTCAC | 166979 |
| rs769065331 | snp | C/T | 1.65225e-05 | 0.00287419 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164169 | TCATCAGGCCTGACA[C/T]AGCAGCTCTGGTTAG | 166979 |
| rs769067543 | snp | A/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55116812 | AATCTTTTCCAAAGC[A/T]TGTACTGAAAACTAT | 166979 |
| rs769101869 | snp | A/T | 1.65067e-05 | 0.00287282 | stop-gained | CDC20B | GRCh38.p7 | 5:55143569 | TTGCATGAGGTGCCT[A/T]GCAAAAATGGAGAGC | 166979 |
| rs769174141 | in-del | -/A/AA | 0.172478 | 0.237742 | intron-variant | CDC20B | GRCh38.p7 | 5:55128398 | AGAGAACATGATGAG[-/A/AA]AAAAAAAAAAACTGG | 166979 |
| rs769177018 | snp | A/G | 1.64776e-05 | 0.00287028 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55119850 | GGTCCACACAGTCAC[A/G]TCATTCTTGGGAGTA | 166979 |
| rs769189130 | snp | C/G | 1.6477e-05 | 0.00287024 | intron-variant, stop-gained | CDC20B | GRCh38.p7 | 5:55120429 | GAGATATTAACCTGT[C/G]AGTTTGTGCTTGGGG | 166979 |
| rs769294310 | snp | A/G | 1.66145e-05 | 0.00288218 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55133512 | GAAGGATTCATCTCT[A/G]ACTCCATCTTTGCAG | 166979 |
| rs769330133 | snp | G/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55155715 | CTATCGCCAGCAGCT[G/T]CCCGCAGGGTCTACA | 166979 |
| rs769333455 | snp | C/G | 1.64768e-05 | 0.00287021 | intron-variant, missense | CDC20B | GRCh38.p7 | 5:55120540 | GACTGCCAGGGACAC[C/G]AATCCATGGCCTTTA | 166979 |
| rs769366957 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55168204 | AAGGCTGTCTCTTGC[A/G]GAGCAGTGCAGGGGA | 166979 |
| rs769373510 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55142184 | CTCCTGGAAGATGAA[C/T]TCTGAAAGTCTCCAC | 166979 |
| rs769400214 | snp | C/T | 1.65479e-05 | 0.0028764 | intron-variant, upstream-variant-2KB, downstream-variant-500B | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170638 | GTATCCAGAGCACTT[C/T]ATTGACAAGAAGAAT | 166979 |
| rs769409871 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55150080 | GAGGTTGCAGTGAGC[C/T]GAGATCGCACCATTG | 166979 |
| rs769414632 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55119448 | GACACATAATGTCTT[A/G]CCCTTTCAGATCGCT | 166979 |
| rs769441782 | snp | A/G | 1.6543e-05 | 0.00287597 | splice-donor-variant | CDC20B | GRCh38.p7 | 5:55146626 | CGTTTGGGGCACCTC[A/G]CCTAGAGTCAAGGTC | 166979 |
| rs769513691 | in-del | -/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55153385 | GTCTGTAGGGCCAAA[-/T]AAATAAAACCCAGAG | 166979 |
| rs769518941 | snp | A/C | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164582 | CAATATCTTATTGTT[A/C]AACTTGACATTTTCT | 166979 |
| rs769526811 | snp | C/T | 1.70659e-05 | 0.00292107 | intron-variant, upstream-variant-2KB, nc-transcript-variant | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170718 | GCAGCCAGCTAACAA[C/T]ACACTGCCTACCTGA | 166979 |
| rs769543463 | snp | A/T | 1.64838e-05 | 0.00287083 | missense, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160311 | TACAACTAAAATTCC[A/T]CAAACCTAAAATCAA | 166979 |
| rs769593739 | snp | C/T | 3.29913e-05 | 0.00406135 | missense, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160209 | TGGAGCCTCTTGCAG[C/T]TTACCCGCTAAAATG | 166979 |
| rs769606134 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55120642 | AGCAGCAAGTCCCCA[C/T]GTCTGCACCTGTCAC | 166979 |
| rs769667322 | in-del | -/TCT | | | intron-variant | CDC20B | GRCh38.p7 | 5:55145689 | TCTCCTTTCCTTCCC[-/TCT]TCTTCTTCCCTACTA | 166979 |
| rs769667429 | snp | G/T | 8.93328e-05 | 0.00668269 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160962 | AATCTTTTGCTTCAC[G/T]TTCCGGTTGGATTTT | 166979 |
| rs769683082 | snp | G/T | 9.10788e-05 | 0.00674768 | missense, upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55172991 | CGGTGCGCTCCAGTT[G/T]CCACTCCATCTCCGG | 166979 |
| rs769712436 | snp | C/T | | | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55163580 | GGTGTGGTCTCAGCT[C/T]ACTGCAACCTCCACC | 166979 |
| rs769754299 | snp | A/C | 9.90393e-05 | 0.00703632 | missense | CDC20B | GRCh38.p7 | 5:55143566 | CCATTGCATGAGGTG[A/C]CTTGCAAAAATGGAG | 166979 |
| rs769774540 | snp | C/T | 3.59234e-05 | 0.00423797 | intron-variant, downstream-variant-500B | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170494 | AAGTACACATAAACA[C/T]ACACTAATTACAGAT | 166979 |
| rs769802207 | snp | A/G/T | 3.34409e-05 | 0.00408893 | intron-variant | CDC20B | GRCh38.p7 | 5:55125033 | GTCTTGACCCACTGC[A/G/T]AGTTTACATAACAAA | 166979 |
| rs769808328 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55155718 | TCGCCAGCAGCTGCC[C/T]GCAGGGTCTACAGAG | 166979 |
| rs769820737 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55127937 | CTAAGTCATTTGCAC[A/G]TGAGTGATATTGTTT | 166979 |
| rs769836080 | snp | C/G | 1.66134e-05 | 0.00288208 | intron-variant, upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55172901 | TTCGGCCCCGCATTA[C/G]AGAGTTAGGGAGAAT | 166979 |
| rs769885792 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55126151 | TTTAAGACCGGCCAA[A/G]AACACAAGATATTCA | 166979 |
| rs769962190 | in-del | -/A | 1.64974e-05 | 0.00287201 | frameshift-variant, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55161169 | AGAATCTTTTGCAAG[-/A]AAAAAACTACGGAGT | 166979 |
| rs769990033 | snp | C/G | 1.64749e-05 | 0.00287005 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55124935 | ATCCGGTGACCACTT[C/G]AGAGCACACACAGCT | 166979 |
| rs770038913 | snp | A/C/T | 6.62991e-05 | 0.00575724 | intron-variant | CDC20B | GRCh38.p7 | 5:55114352 | ACAGTTCATACTCCT[A/C/T]CACGTTACATGGGCT | 166979 |
| rs770055340 | snp | A/T | 1.89842e-05 | 0.00308086 | intron-variant | CDC20B | GRCh38.p7 | 5:55128391 | TAATACACAGAGAAC[A/T]TGATGAGAAAAAAAA | 166979 |
| rs770058397 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55121493 | TATTGGGTTGGGTTA[A/G]TTTTTTTTGGAAAGG | 166979 |
| rs770080562 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55151417 | AAGGGAGGAGACACC[A/G]CATTGGAAGATAAAC | 166979 |
| rs770087593 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55129724 | CAAGTCTCAGCCTAG[A/G]CTCTGATCCACATGT | 166979 |
| rs770196081 | in-del | -/AT/T | | | intron-variant, utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55136576 | AAAAAAAAAAAAAAA[-/AT/T]TAGGACAAGCCATAA | 166979 |
| rs770208961 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55123004 | GAGTAATTTGTTGCA[C/T]AGCAATAGATAACCA | 166979 |
| rs770241735 | snp | A/G | | | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55158242 | GATCCCACTTAGAGA[A/G]CAAGGCCAGAGAGCT | 166979 |
| rs770293059 | snp | C/T | 1.65029e-05 | 0.00287248 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164157 | AGCCCATTGAAGTCA[C/T]CAGGCCTGACATAGC | 166979 |
| rs770342468 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55116188 | ACCACTGTCTATTAT[C/T]TAAAAAATAATAAAC | 166979 |
| rs770483355 | snp | A/G | 0.000428527 | 0.0146315 | missense, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160267 | AGTTTTGCTGTCTAT[A/G]GTTCTATGCACAGTA | 166979 |
| rs770500089 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55154432 | TAAGGTGGGAGGATT[A/G]CTTGATCCTGGGAGG | 166979 |
| rs770542719 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55117968 | AAAAATACACACAAA[A/C]ATTAGCCAGGCGTGG | 166979 |
| rs770553085 | snp | C/G | 1.6477e-05 | 0.00287024 | missense | CDC20B | GRCh38.p7 | 5:55119863 | ACATCATTCTTGGGA[C/G]TACCTTGACCAGTTG | 166979 |
| rs770693531 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55151239 | TATTAGAAATTTAGA[A/C]TTTTCATATGAATTT | 166979 |
| rs770702643 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55166980 | GGTTGCAATGAGCCA[A/G]GATTGCACCACTGCA | 166979 |
| rs770727999 | snp | C/G | 1.65228e-05 | 0.00287422 | utr-variant-5-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160186 | CTTCCCTCTAGAATC[C/G]TCCAACATGGAGCCT | 166979 |
| rs770744231 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55141689 | TGGTATTTTGTTTTT[C/T]TTCCTTGATGTTATG | 166979 |
| rs770749493 | snp | A/G | 1.6483e-05 | 0.00287076 | intron-variant | CDC20B | GRCh38.p7 | 5:55120393 | GATTCCAGAAGATCA[A/G]AATGAAGATGAAGCC | 166979 |
| rs770772490 | snp | C/T | 1.6473e-05 | 0.00286988 | missense, upstream-variant-2KB | CDC20B, MIR449A, MIR449B, MIR449C | GRCh38.p7 | 5:55172613 | TCTTGACTTCTCTTC[C/T]GCTTCAAGTCTTTGG | 166979 |
| rs770924971 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55140123 | GAAGAACTAAAGGTG[A/G]TCACCTATAGAGAAT | 166979 |
| rs771017172 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55155442 | GTAGCAAAGACAGCC[C/T]AGGTAGCTCTGAAGC | 166979 |
| rs771059473 | snp | A/T | 1.65842e-05 | 0.00287955 | missense, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55161222 | ATTAAGATTCTAGGA[A/T]CTGAAGGAGAACCTG | 166979 |
| rs771078663 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55134324 | ACACCAAGAAACCAA[A/G]TTGTTACTCATAAAT | 166979 |
| rs771108187 | snp | G/T | 1.64928e-05 | 0.00287161 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55124848 | CAGCGGTTGGCCCTG[G/T]GCACTGGCACCTGGA | 166979 |
| rs771180492 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55149978 | ATCTCTACTAAAAAT[A/G]CAAAAATTAGCCAGC | 166979 |
| rs771193908 | snp | A/C | 3.29717e-05 | 0.00406015 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55127289 | ATTCCAGCTCAGAGC[A/C]CCAACTACTGACAAA | 166979 |
| rs771210372 | snp | C/T | 3.29571e-05 | 0.00405924 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55146683 | TGATCCGGAAGCTTC[C/T]GGGAGGTAGGTGGTT | 166979 |
| rs771220208 | in-del | -/AA | | | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55162092 | AAACCATATTAGTCA[-/AA]AAAAAAAAAAAAAAA | 166979 |
| rs771225112 | snp | A/G | | | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55163331 | GTTCAAGCCCATCCC[A/G]GGCAACACAGCGAGA | 166979 |
| rs771228222 | snp | A/G | | | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55158170 | GAAGTCTGGGGTGGG[A/G]CCCAAAATGCTGTGT | 166979 |
| rs771330126 | snp | A/T | 1.72181e-05 | 0.00293407 | intron-variant | CDC20B | GRCh38.p7 | 5:55140416 | GGCATTTCTGAAAAT[A/T]AACACACATAAGGAG | 166979 |
| rs771390476 | snp | G/T | | | intron-variant, upstream-variant-2KB | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55171213 | AGCTACTCAGGAGGC[G/T]GAGACATGAGAATCA | 166979 |
| rs771466461 | snp | A/C | | | intron-variant, upstream-variant-2KB, downstream-variant-500B | CDC20B, MIR449A, MIR449B, MIR449C | GRCh38.p7 | 5:55172094 | ATTTAAATTTGTTTC[A/C]TTTTACACTGATTAC | 166979 |
| rs771475794 | snp | A/C | 3.30382e-05 | 0.00406423 | missense | CDC20B | GRCh38.p7 | 5:55114262 | CATCAGCTGCAGCAG[A/C]AAACACCCGGGTCTG | 166979 |
| rs771490473 | snp | G/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164931 | TTTTCAGTATTTCTC[G/T]CTGCATTATTTTTTA | 166979 |
| rs771496764 | snp | A/C | 1.64779e-05 | 0.00287031 | missense | CDC20B | GRCh38.p7 | 5:55146801 | ACCTCTGCGGACAGC[A/C]TCTTCGCAAAGTTGC | 166979 |
| rs771517372 | snp | A/G | 1.95463e-05 | 0.00312615 | intron-variant | CDC20B | GRCh38.p7 | 5:55128374 | AGTCAATTATAGTGT[A/G]ATAATACACAGAGAA | 166979 |
| rs771563192 | in-del | -/CGTAGACTG | 3.32242e-05 | 0.00407566 | cds-indel | CDC20B | GRCh38.p7 | 5:55124812 | TCTTACCTTGACTGC[-/CGTAGACTG]GGTTATGACTTTCAG | 166979 |
| rs771581323 | in-del | -/AG | 8.74027e-05 | 0.00661012 | intron-variant | CDC20B | GRCh38.p7 | 5:55140267 | AGAAATGAAGGAGGC[-/AG]AGAGAGAGGAGCGCA | 166979 |
| rs771607459 | snp | A/G | 1.65919e-05 | 0.00288022 | utr-variant-5-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160167 | GAATTCCAGGCTGCT[A/G]AGACTTCCCTCTAGA | 166979 |
| rs771634015 | snp | A/C | 1.64846e-05 | 0.0028709 | intron-variant, upstream-variant-2KB | CDC20B, MIR449B, MIR449C | GRCh38.p7 | 5:55172676 | ACAGATAACATATTG[A/C]GGGAGAAACTATTTA | 166979 |
| rs771639463 | in-del | -/T | 1.64947e-05 | 0.00287177 | frameshift-variant | CDC20B | GRCh38.p7 | 5:55114312 | GCAGCACTCTGCCCC[-/T]TGTGGCCTGGGGGAA | 166979 |
| rs771651883 | in-del | -/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55132780 | CCAGTCCCCAATGTA[-/T]CTTCTTCATTGCCAT | 166979 |
| rs771661014 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55165912 | TTAAGTGACCAGGAA[A/G]GAAATCAGAACTAAC | 166979 |
| rs771706225 | snp | A/G | 1.69496e-05 | 0.0029111 | intron-variant | CDC20B | GRCh38.p7 | 5:55128403 | AACATGATGAGAAAA[A/G]AAAAAACTGGCCAGT | 166979 |
| rs771792630 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55123402 | TTTTATATTTATTAA[C/T]AATCATTTTCTTAAA | 166979 |
| rs771864464 | snp | G/T | 4.94173e-05 | 0.00497053 | missense, upstream-variant-2KB | CDC20B, MIR449A, MIR449B, MIR449C | GRCh38.p7 | 5:55172588 | AAGCCCTGGACTCAC[G/T]TTGGCGGAATCTTGA | 166979 |
| rs771944297 | snp | A/G | 1.64754e-05 | 0.00287009 | missense | CDC20B | GRCh38.p7 | 5:55124906 | TCACTGCAGCCGCTG[A/G]AAAGCAGCCTGCCAT | 166979 |
| rs772094097 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55153084 | TCTGAACAAAAAATA[C/T]AAAAATTAGCTGGGC | 166979 |
| rs772138250 | snp | A/G | 1.70246e-05 | 0.00291754 | intron-variant | CDC20B | GRCh38.p7 | 5:55133554 | CAAACACTTCTACAC[A/G]GCTCTAAGATCCTGA | 166979 |
| rs772170709 | snp | G/T | 4.9489e-05 | 0.00497414 | missense | CDC20B | GRCh38.p7 | 5:55127271 | CCTGCTGAGGATAAA[G/T]TGATTCCAGCTCAGA | 166979 |
| rs772247936 | snp | A/G | 1.66496e-05 | 0.00288522 | missense, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55161015 | CTAGTTGTAAACGTG[A/G]CCAGTGACTGCCAAC | 166979 |
| rs772374267 | snp | A/G | 3.29984e-05 | 0.00406179 | missense, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55161172 | AATCTTTTGCAAGAA[A/G]AAACTACGGAGTAAC | 166979 |
| rs772381790 | snp | C/T | | | intron-variant, upstream-variant-2KB | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55171129 | GACCAGCCTGGCCAA[C/T]ATGGTGAAACCCCGT | 166979 |
| rs772402351 | in-del | -/AAGAAAA | | | intron-variant | CDC20B | GRCh38.p7 | 5:55154519 | GAGACCGTGTCTCCC[-/AAGAAAA]AAGAAAAAAGAGGAA | 166979 |
| rs772421727 | snp | A/G | 1.67562e-05 | 0.00289444 | intron-variant | CDC20B | GRCh38.p7 | 5:55146607 | TTGCAAAACGGGGCT[A/G]TGGCGTTTGGGGCAC | 166979 |
| rs772439162 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55155834 | GCTCTGCAGACCTCC[C/T]GTGGCCCCTTCCAGA | 166979 |
| rs772452868 | in-del | -/T | 1.855e-05 | 0.00304543 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160443 | ATTTTTCCTTGTCTC[-/T]TGTTTATTCCTCTTA | 166979 |
| rs772475010 | snp | C/T | | | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55159768 | ACCATATGAGTAGGT[C/T]ACATTTAATCTACAT | 166979 |
| rs772555481 | in-del | -/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55121521 | GGAGTATTTTTTTTG[-/T]TTTTTGTGCGTGTGT | 166979 |
| rs772621131 | snp | C/T | 1.72356e-05 | 0.00293556 | intron-variant | CDC20B | GRCh38.p7 | 5:55125067 | ATTAAGCCCTGTTGC[C/T]ACATAAACATTTGAA | 166979 |
| rs772640157 | snp | A/C | 4.97418e-05 | 0.00498682 | utr-variant-5-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160170 | TTCCAGGCTGCTGAG[A/C]CTTCCCTCTAGAATC | 166979 |
| rs772712334 | snp | C/T | | | intron-variant, downstream-variant-500B | GPX8, CDC20B | GRCh38.p7 | 5:55167532 | ATTTCAATCTACCAC[C/T]GGTTTAGTAACTAGG | 166979 |
| rs772726644 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55149828 | CTAAAGACCACTGAA[C/T]TGGTGACTTAAAAGG | 166979 |
| rs772798784 | snp | G/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55151558 | TTTAAAAGAGGAAAT[G/T]AAAGAATAATAATTG | 166979 |
| rs772799447 | in-del | -/GGT | | | intron-variant | CDC20B | GRCh38.p7 | 5:55157819 | GGGCCCTGCCTAAGC[-/GGT]GGTCAGTCAACATCC | 166979 |
| rs772834191 | snp | A/G | 1.65562e-05 | 0.00287712 | intron-variant, upstream-variant-2KB | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170781 | AGTCACTGAGGCTAA[A/G]TTTGTAACATGAAAC | 166979 |
| rs772846200 | snp | G/T | 1.65433e-05 | 0.002876 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164174 | AGGCCTGACATAGCA[G/T]CTCTGGTTAGACAAG | 166979 |
| rs772881922 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55166099 | TGTATCCTCACCTAC[A/G]CCTTCCATGAACTCA | 166979 |
| rs772892084 | snp | A/C | 1.69309e-05 | 0.0029095 | intron-variant | CDC20B | GRCh38.p7 | 5:55128404 | ACATGATGAGAAAAA[A/C]AAAAACTGGCCAGTA | 166979 |
| rs772937500 | snp | A/G | 1.64776e-05 | 0.00287028 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55119853 | CCACACAGTCACATC[A/G]TTCTTGGGAGTACCT | 166979 |
| rs772943677 | snp | C/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164935 | CAGTATTTCTCTCTG[C/T]ATTATTTTTTAGAAG | 166979 |
| rs772950577 | snp | C/G | 0.000131957 | 0.00812163 | missense | CDC20B | GRCh38.p7 | 5:55124845 | TTTCAGCGGTTGGCC[C/G]TGTGCACTGGCACCT | 166979 |
| rs772951618 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55120077 | CTAGGAAAGTTTATC[A/C]CAAGGCAACAAAGGA | 166979 |
| rs773021568 | snp | C/T | 1.64792e-05 | 0.00287042 | missense | CDC20B | GRCh38.p7 | 5:55128507 | AGTTACAAGTGAGAC[C/T]TAAGTCTATGTTTTC | 166979 |
| rs773025490 | snp | G/T | 1.65861e-05 | 0.00287972 | intron-variant | CDC20B | GRCh38.p7 | 5:55114358 | CATACTCCTCCACGT[G/T]ACATGGGCTGCTGCT | 166979 |
| rs773048958 | snp | A/G | | | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55159787 | TTTAATCTACATTCT[A/G]AACTATTGCTGAGCA | 166979 |
| rs773063267 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55139971 | GGCAAAGGTTGCAGT[A/G]AGCCAAGATCGCACC | 166979 |
| rs773079313 | snp | A/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55138398 | ACTCCTGGTTTCAAG[A/T]GATCCACTGCCTCGG | 166979 |
| rs773140373 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55149068 | GTTTACCAGTGGAGA[A/C]CTGACTAGGCAAACT | 166979 |
| rs773148641 | in-del | -/A | 1.68667e-05 | 0.00290397 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55161261 | TTCTTGTTGGTAAAT[-/A]ATCTGCCTTGCATAT | 166979 |
| rs773206412 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon, upstream-variant-2KB | CDC20B, MIR449A, MIR449B, MIR449C | GRCh38.p7 | 5:55172591 | CCCTGGACTCACGTT[A/G]GCGGAATCTTGACTT | 166979 |
| rs773242607 | snp | A/G | | | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55161757 | AAAAACATATAACTT[A/G]GTTTTTTCAGAGGGC | 166979 |
| rs773278697 | snp | C/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55167202 | TTGTTTTCTTTGGTG[C/T]GTAGAGAAGAATACT | 166979 |
| rs773338405 | snp | C/T | 1.65507e-05 | 0.00287664 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55114254 | GGCCGTCCCATCAGC[C/T]GCAGCAGAAAACACC | 166979 |
| rs773414654 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55142579 | CTCCAATCAGCAGTA[A/G]AGGGTGGAAAACACA | 166979 |
| rs773429830 | snp | A/C | 3.29614e-05 | 0.00405951 | intron-variant | CDC20B | GRCh38.p7 | 5:55120577 | CACATAATAGCACAG[A/C]CAGGTCAGCTTCAAA | 166979 |
| rs773453088 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55131591 | TCGGTATGAAGTCTA[A/G]GAAGTAACTGTTGGC | 166979 |
| rs773459703 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55119646 | AACATTCAACTATAC[A/G]CTCTCTGAGGTAGGG | 166979 |
| rs773508181 | snp | C/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55148208 | AATCTCACTAGCAAT[C/G]AAAGAAATGCAAATT | 166979 |
| rs773510572 | snp | C/G | 1.66646e-05 | 0.00288652 | intron-variant | CDC20B | GRCh38.p7 | 5:55140304 | GAAGGACAATGTCTT[C/G]ATCCTGTACCTTTCC | 166979 |
| rs773515483 | snp | A/C | 3.42612e-05 | 0.00413877 | intron-variant | CDC20B | GRCh38.p7 | 5:55133558 | CACTTCTACACAGCT[A/C]TAAGATCCTGAAAAT | 166979 |
| rs773546541 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55156796 | GGAGAATCACTCAAA[C/T]CCAAGAGATGGAGGT | 166979 |
| rs773600557 | snp | A/G | 1.65083e-05 | 0.00287296 | synonymous-codon, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55161182 | AAGAAAAAACTACGG[A/G]GTAACTTTCCCCATC | 166979 |
| rs773669053 | snp | G/T | 1.6736e-05 | 0.0028927 | intron-variant | CDC20B | GRCh38.p7 | 5:55146608 | TGCAAAACGGGGCTG[G/T]GGCGTTTGGGGCACC | 166979 |
| rs773725442 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164868 | CTGACATATATAAAT[A/G]GTCATTTATAAATGA | 166979 |
| rs773730782 | snp | C/T | 1.73366e-05 | 0.00294415 | intron-variant | CDC20B | GRCh38.p7 | 5:55125071 | AGCCCTGTTGCTACA[C/T]AAACATTTGAAAACA | 166979 |
| rs773815311 | snp | A/G/T | 3.29822e-05 | 0.00406082 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55114272 | AGCAGAAAACACCCG[A/G/T]GTCTGGTCTGGACTC | 166979 |
| rs773841371 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55139657 | GTGTAGTAATATGAT[A/G]TAAACATTAACTACT | 166979 |
| rs773912193 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55128223 | TGTGGTGGAAACTAA[C/T]CAGAGTATCCTTACG | 166979 |
| rs773938853 | snp | A/G | | | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55163728 | GGGCAGGCTGGTCTT[A/G]AACTCCTGATCTTAG | 166979 |
| rs774052587 | snp | C/G | 1.69209e-05 | 0.00290864 | intron-variant | CDC20B | GRCh38.p7 | 5:55133545 | TACAAGAAACAAACA[C/G]TTCTACACAGCTCTA | 166979 |
| rs774121210 | in-del | -/AAC | | | intron-variant | CDC20B | GRCh38.p7 | 5:55130493 | GGCCACAGTCAATGG[-/AAC]AACATCTTTTAAATG | 166979 |
| rs774166912 | snp | C/G | 1.65515e-05 | 0.00287671 | intron-variant, upstream-variant-2KB, nc-transcript-variant | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170647 | GCACTTCATTGACAA[C/G]AAGAATTTATCCAGA | 166979 |
| rs774174254 | snp | A/G | 1.6483e-05 | 0.00287076 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55127304 | CCCAACTACTGACAA[A/G]TGACCAAGCATATTT | 166979 |
| rs774178279 | snp | C/T | 3.29495e-05 | 0.00405877 | missense | CDC20B | GRCh38.p7 | 5:55146775 | TGGTAATGGGGCTAC[C/T]CGCAACAGGAACCTC | 166979 |
| rs774210520 | snp | A/G | 3.30409e-05 | 0.0040644 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55124827 | CGTAGACTGGGTTAT[A/G]ACTTTCAGCGGTTGG | 166979 |
| rs774212603 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55151505 | GCAAAATTCCAAAGA[A/C]ATTCTAAACTTTAAA | 166979 |
| rs774231285 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55152800 | TATCTTACTATCCTC[A/G]GGACATTGGTATCTA | 166979 |
| rs774292084 | snp | A/G | 1.64784e-05 | 0.00287035 | intron-variant | CDC20B | GRCh38.p7 | 5:55120555 | CAATCCATGGCCTTT[A/G]AAGTTTCACATAATA | 166979 |
| rs774339663 | snp | A/C | 0.000232728 | 0.0107847 | intron-variant, upstream-variant-2KB | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170769 | CGTGGCCCAGGCAGT[A/C]ACTGAGGCTAAATTT | 166979 |
| rs774343233 | snp | A/C | | | upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55174335 | GCATTAGAACTAAGA[A/C]CCAATCTTAGACCAG | 166979 |
| rs774422724 | snp | A/G | 1.67711e-05 | 0.00289573 | synonymous-codon, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160999 | TTTCCGGGAGGTTTC[A/G]CTAGTTGTAAACGTG | 166979 |
| rs774506933 | in-del | -/CT | | | intron-variant | CDC20B | GRCh38.p7 | 5:55145830 | TCTCTTGCTTCCTTC[-/CT]CTTACTTTCTCTTCC | 166979 |
| rs774513616 | snp | G/T | | | intron-variant, downstream-variant-500B | CDC20B | GRCh38.p7 | 5:55136213 | GGCCTCCCAAAGTGC[G/T]GGGATTATAGGCGTG | 166979 |
| rs774516213 | snp | C/T | 1.64827e-05 | 0.00287073 | utr-variant-5-prime, upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55173014 | ATCTCCGGCTGACTT[C/T]GCCCTGCCTGGCGTT | 166979 |
| rs774552194 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55154516 | AGTGAGACCGTGTCT[C/T]CCAAGAAAAAAGAAA | 166979 |
| rs774560100 | snp | A/C | 1.70414e-05 | 0.00291898 | intron-variant | CDC20B | GRCh38.p7 | 5:55125058 | AACAAAAAAATTAAG[A/C]CCTGTTGCTACATAA | 166979 |
| rs774586943 | in-del | -/T | 3.30049e-05 | 0.00406219 | frameshift-variant | CDC20B | GRCh38.p7 | 5:55124995 | TGGGCTACCCGAACA[-/T]TCGTGATGATAAACA | 166979 |
| rs774607635 | snp | C/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55167134 | AGGAAAAGGACAAAA[C/T]CAAATGCATTTTAAC | 166979 |
| rs774619146 | snp | C/T | 1.7047e-05 | 0.00291945 | intron-variant | CDC20B | GRCh38.p7 | 5:55133404 | TCCCAATCTAAATGA[C/T]AACTTACAGTAGTCA | 166979 |
| rs774635719 | snp | A/G | 4.94809e-05 | 0.00497373 | missense, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160359 | AAGTGAAGGATGCAA[A/G]AGGAAGAACTGTTTC | 166979 |
| rs774644876 | snp | C/G | | | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55158574 | GAACCAGAAGAGCAG[C/G]CAGCACCCTGAGCAC | 166979 |
| rs774661008 | snp | A/G | | | upstream-variant-2KB | CDC20B | GRCh38.p7 | 5:55174937 | AAGTATTAGTCAAAT[A/G]TCTTTAGGAAGTAAT | 166979 |
| rs774665026 | snp | C/T | 9.90213e-05 | 0.00703569 | missense | CDC20B | GRCh38.p7 | 5:55124997 | GGGCTACCCGAACAT[C/T]GTGATGATAAACACG | 166979 |
| rs774745351 | snp | A/G | 1.92569e-05 | 0.00310291 | intron-variant | CDC20B | GRCh38.p7 | 5:55140449 | TATTTCTTTAAAAAC[A/G]TACATGTACAACTAA | 166979 |
| rs774745711 | snp | C/T | 1.69046e-05 | 0.00290723 | intron-variant, downstream-variant-500B | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170522 | GATTCAGTTACACTC[C/T]GATGTTCATTGTATA | 166979 |
| rs774874806 | in-del | -/A | 1.76533e-05 | 0.00297092 | intron-variant | CDC20B | GRCh38.p7 | 5:55140425 | AAAATAAACACACAT[-/A]AAGGAGAATATTTCT | 166979 |
| rs774926432 | snp | A/C | 8.23825e-05 | 0.00641751 | intron-variant, missense | CDC20B | GRCh38.p7 | 5:55120544 | GCCAGGGACACCAAT[A/C]CATGGCCTTTAAAGT | 166979 |
| rs774949170 | snp | A/C | 0.117188 | 0.211804 | intron-variant | CDC20B | GRCh38.p7 | 5:55126371 | AGGCATGGTGGTGGG[A/C]GCCTGTAGTCCCAGC | 166979 |
| rs774996549 | snp | G/T | 5.1788e-05 | 0.00508835 | intron-variant, upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55172920 | GTTAGGGAGAATGCA[G/T]AAAAGGGTGTTACTC | 166979 |
| rs775039033 | snp | A/G | 1.65239e-05 | 0.00287431 | missense | CDC20B | GRCh38.p7 | 5:55146630 | TGGGGCACCTCACCT[A/G]GAGTCAAGGTCTCTT | 166979 |
| rs775042463 | in-del | -/TTTTTT | | | intron-variant, upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55172752 | TGTCAGATTACACTT[-/TTTTTT]TTTTTTTTTTTTTTT | 166979 |
| rs775102850 | in-del | -/A | | | intron-variant | CDC20B | GRCh38.p7 | 5:55124356 | AATGGCTTCTTATCC[-/A]GCGCCCATCTGGAAG | 166979 |
| rs775191808 | snp | A/G | 3.29554e-05 | 0.00405914 | missense | CDC20B | GRCh38.p7 | 5:55146685 | ATCCGGAAGCTTCTG[A/G]GAGGTAGGTGGTTGA | 166979 |
| rs775192725 | snp | C/T | 1.65482e-05 | 0.00287643 | intron-variant, upstream-variant-2KB, downstream-variant-500B | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170640 | ATCCAGAGCACTTCA[C/T]TGACAAGAAGAATTT | 166979 |
| rs775215685 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55120650 | GTCCCCACGTCTGCA[A/C]CTGTCACAGCTCTCC | 166979 |
| rs775252875 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55140297 | CAGGAAAGAAGGACA[A/C]TGTCTTGATCCTGTA | 166979 |
| rs775337124 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55134481 | CAAAAAAACTCCTGG[A/G]GCTGGGCACGGTGGC | 166979 |
| rs775369733 | snp | G/T | | | utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55113243 | TCAAAAGACAGAACA[G/T]CGAACTGATCAAGTT | 166979 |
| rs775434759 | snp | A/G | 1.7271e-05 | 0.00293857 | intron-variant | CDC20B | GRCh38.p7 | 5:55133387 | TCATTTCAACTTTTA[A/G]TTCCCAATCTAAATG | 166979 |
| rs775439560 | snp | C/T | 1.64776e-05 | 0.00287028 | intron-variant, missense | CDC20B | GRCh38.p7 | 5:55120433 | TATTAACCTGTGAGT[C/T]TGTGCTTGGGGTCTG | 166979 |
| rs775546506 | snp | A/G | 2.29098e-05 | 0.00338443 | missense, upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55172994 | TGCGCTCCAGTTTCC[A/G]CTCCATCTCCGGCTG | 166979 |
| rs775634593 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55128058 | AGAAAAAAAAATTCA[C/T]TCATTTTCTATAACT | 166979 |
| rs775678600 | snp | C/G/T | 4.95228e-05 | 0.00497588 | synonymous-codon, missense | CDC20B | GRCh38.p7 | 5:55143567 | CATTGCATGAGGTGC[C/G/T]TTGCAAAAATGGAGA | 166979 |
| rs775681987 | snp | C/T | 1.64944e-05 | 0.00287175 | missense, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160211 | GAGCCTCTTGCAGCT[C/T]ACCCGCTAAAATGTT | 166979 |
| rs775695518 | in-del | -/C | 3.46855e-05 | 0.00416432 | intron-variant | CDC20B | GRCh38.p7 | 5:55146580 | CTCTCAGGAATATAT[-/C]TTTTATTCACGTTGC | 166979 |
| rs775741617 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55133083 | ACAAGCTGGGCACAT[A/G]ACAAGTAGACCCAAT | 166979 |
| rs775742045 | in-del | -/T | 5.04902e-05 | 0.0050242 | intron-variant | CDC20B | GRCh38.p7 | 5:55125041 | CACTGCGAGTTTACA[-/T]TAACAAAAAAATTAA | 166979 |
| rs775742835 | snp | A/T | | | intron-variant, upstream-variant-2KB, nc-transcript-variant | CDC20B, MIR449A, MIR449B, MIR449C | GRCh38.p7 | 5:55172347 | TGCCTACCTGACACA[A/T]CCCAGCTTTATCCTT | 166979 |
| rs775751337 | snp | C/G | 1.64746e-05 | 0.00287002 | missense | CDC20B | GRCh38.p7 | 5:55124939 | GGTGACCACTTCAGA[C/G]CACACACAGCTTGCT | 166979 |
| rs775786567 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55131370 | TAAGATCAATTAAAA[C/T]AGAACAGAAGTAAAA | 166979 |
| rs775796372 | snp | A/G | | | intron-variant, upstream-variant-2KB | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55171395 | TACTTGTCTGTATTA[A/G]ACAGTAAAATATCTA | 166979 |
| rs775801096 | snp | C/G/T | 0.000115467 | 0.00759752 | missense | CDC20B | GRCh38.p7 | 5:55124990 | TGATGCTGGGCTACC[C/G/T]GAACATCGTGATGAT | 166979 |
| rs775848373 | snp | A/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55120329 | ATGGACTCAATAGAG[A/T]AAGAGAGCTTGTTGG | 166979 |
| rs775978618 | snp | G/T | 1.65081e-05 | 0.00287293 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164161 | CATTGAAGTCATCAG[G/T]CCTGACATAGCAGCT | 166979 |
| rs775984104 | snp | C/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55166199 | CCAGCACCACATGGG[C/T]AGCAGAGACTCCCCA | 166979 |
| rs776073845 | snp | C/T | 1.7389e-05 | 0.0029486 | intron-variant | CDC20B | GRCh38.p7 | 5:55133365 | CCAGAGCACAGGATG[C/T]ATTTTGTCATTTCAA | 166979 |
| rs776124138 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55146025 | TACATATATACATAT[A/G]CATTCATACAATCTT | 166979 |
| rs776135130 | snp | C/T | 1.65075e-05 | 0.00287289 | missense | CDC20B | GRCh38.p7 | 5:55143628 | CTGGGGGTCTTCAGT[C/T]GTTCTTTGCGGGATC | 166979 |
| rs776153488 | snp | G/T | 1.67147e-05 | 0.00289086 | intron-variant, downstream-variant-500B | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170531 | ACACTCTGATGTTCA[G/T]TGTATATGCAATAAG | 166979 |
| rs776238628 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55138592 | GAGAAGCCAAAGTAA[A/G]TGGGGGGTTGGAGGG | 166979 |
| rs776254515 | in-del | -/TCTATTGG | 1.76979e-05 | 0.00297466 | intron-variant | CDC20B | GRCh38.p7 | 5:55124785 | CAGGAAACCTAGAAA[-/TCTATTGG]TCTATTGGGTTTCTT | 166979 |
| rs776268075 | snp | C/T | | | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55163464 | GGTGGCACACACCTG[C/T]AATCCCAGCAATTTG | 166979 |
| rs776273570 | snp | C/T | 1.6477e-05 | 0.00287024 | missense | CDC20B | GRCh38.p7 | 5:55119876 | GAGTACCTTGACCAG[C/T]TGCAATCTCCTTTGT | 166979 |
| rs776279367 | snp | C/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55167013 | CCAACCTGGGCAACA[C/G]AGCGAGACCCCATCT | 166979 |
| rs776313796 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55154441 | AGGATTGCTTGATCC[C/T]GGGAGGTCGACGCTG | 166979 |
| rs776336592 | snp | C/T | 3.30923e-05 | 0.00406756 | intron-variant, upstream-variant-2KB, downstream-variant-500B | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170635 | CAGGTATCCAGAGCA[C/T]TTCATTGACAAGAAG | 166979 |
| rs776339409 | in-del | -/AAT | | | intron-variant | CDC20B | GRCh38.p7 | 5:55145291 | CTGTCGTTACATGGG[-/AAT]AATTTCATTGATTTG | 166979 |
| rs776365940 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55153467 | ATGACAAATAAGAAA[A/C]ATACATGCCCCCTGA | 166979 |
| rs776411353 | in-del | -/TATACT | | | intron-variant | CDC20B | GRCh38.p7 | 5:55169157 | TATTTACATGGAAGA[-/TATACT]TAAACATAAATCTCC | 166979 |
| rs776456420 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55149167 | TAAACCACACCAAAG[A/C]ACCACTTCACACCCA | 166979 |
| rs776536017 | in-del | -/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55138349 | GTTTTTACTAGAGAT[-/G]GGGGTCTCACCATGT | 166979 |
| rs776583268 | snp | A/G | 1.65116e-05 | 0.00287324 | missense, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160193 | CTAGAATCCTCCAAC[A/G]TGGAGCCTCTTGCAG | 166979 |
| rs776616363 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55169238 | GAAAGTAGTAAAATG[C/T]GTAAGAATCAAATTA | 166979 |
| rs776687157 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55156066 | TTCCACATGGCTAGG[A/G]AGTCCTCACAATCAT | 166979 |
| rs776703772 | in-del | -/TGAC | 0.000164739 | 0.00907428 | frameshift-variant | CDC20B | GRCh38.p7 | 5:55146698 | TGGGAGGTAGGTGGT[-/TGAC]TGCTCTTCCCCAAAG | 166979 |
| rs776791651 | in-del | -/CAAT | 8.24314e-05 | 0.00641942 | frameshift-variant, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55161113 | GTTGGCTTTTCCCTG[-/CAAT]CAGTTTGGAGAATCG | 166979 |
| rs776875721 | snp | A/T | | | missense, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160260 | TATTTGCAGTTTTGC[A/T]GTCTATAGTTCTATG | 166979 |
| rs776895073 | snp | A/T | 1.66164e-05 | 0.00288235 | intron-variant | CDC20B | GRCh38.p7 | 5:55140311 | AATGTCTTGATCCTG[A/T]ACCTTTCCAAACACA | 166979 |
| rs776934199 | snp | A/G | 3.29522e-05 | 0.00405894 | missense | CDC20B | GRCh38.p7 | 5:55124924 | AGCAGCCTGCCATCC[A/G]GTGACCACTTCAGAG | 166979 |
| rs776959543 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55145813 | CCATCCCCTCATCCC[C/T]CTCTCTTGCTTCCTT | 166979 |
| rs777016138 | snp | C/T | 1.64906e-05 | 0.00287142 | missense | CDC20B | GRCh38.p7 | 5:55124852 | GGTTGGCCCTGTGCA[C/T]TGGCACCTGGATCGT | 166979 |
| rs777052830 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55133138 | ACCCATATTTAAAAT[A/C]CATACATAAGAATAG | 166979 |
| rs777092225 | snp | C/T | 1.64857e-05 | 0.00287099 | missense | CDC20B | GRCh38.p7 | 5:55127290 | TTCCAGCTCAGAGCC[C/T]CAACTACTGACAAAT | 166979 |
| rs777117585 | in-del | -/TTG | 1.72877e-05 | 0.00293999 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160421 | ATCATCTGATTTTTA[-/TTG]TTATCATTTTTCCTT | 166979 |
| rs777145572 | snp | A/C/T | 3.30131e-05 | 0.00406269 | missense | CDC20B | GRCh38.p7 | 5:55114270 | GCAGCAGAAAACACC[A/C/T]GGGTCTGGTCTGGAC | 166979 |
| rs777162567 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55131271 | ACAATAGTAACTCTA[C/T]GTAGACTAAGAAAGT | 166979 |
| rs777202382 | snp | A/G | 0.000115541 | 0.00759982 | missense, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55161058 | ATTACTTAGGGCTGA[A/G]GGAACTGCACAAAGA | 166979 |
| rs777211089 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55126424 | GTGAGCTGAGATCAC[A/G]CCACTGAACTCCAGC | 166979 |
| rs777226102 | snp | A/G | 1.73363e-05 | 0.00294412 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160423 | CATCTGATTTTTATT[A/G]TTATCATTTTTCCTT | 166979 |
| rs777322411 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55121462 | TTGGTTTTTTGTTGT[A/G]TTGTGGTTTGATTTG | 166979 |
| rs777328874 | snp | C/T | | | utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55113893 | GGGAGAAAAGTCATA[C/T]GGGAAAGAAGTAGAA | 166979 |
| rs777336440 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55150484 | CTGCTCTGTGCTCTC[C/T]CCACCAGCTGACCAA | 166979 |
| rs777385145 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55141461 | AGCCAAGTGATGGCC[C/T]TCCCGGTGTTATAAC | 166979 |
| rs777400974 | in-del | -/A | 1.6498e-05 | 0.00287206 | intron-variant, upstream-variant-2KB | CDC20B, MIR449B, MIR449C | GRCh38.p7 | 5:55172693 | GAGAAACTATTTAGG[-/A]AAAATCATAATTTCA | 166979 |
| rs777435086 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55155361 | GTGGGTTGGAAAAAC[C/T]TAGACATCCCAGAAA | 166979 |
| rs777504613 | snp | A/C | 1.82171e-05 | 0.00301798 | intron-variant | CDC20B | GRCh38.p7 | 5:55128659 | ATAATTATACAGCCA[A/C]ATGAAAACATGTTCA | 166979 |
| rs777532280 | snp | C/T | 1.64779e-05 | 0.00287031 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55124965 | TTGCTTGTGGCGAAG[C/T]GTTCCAACATGATGC | 166979 |
| rs777548312 | snp | A/G | 3.29954e-05 | 0.0040616 | intron-variant, upstream-variant-2KB | CDC20B, MIR449B, MIR449C | GRCh38.p7 | 5:55172693 | GGAGAAACTATTTAG[A/G]AAAATCATAATTTCA | 166979 |
| rs777567014 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55118997 | CTCTTGTTCACCTGT[A/G]TATCCCCAGCACCCC | 166979 |
| rs777602153 | snp | A/G | 8.23744e-05 | 0.0064172 | missense | CDC20B | GRCh38.p7 | 5:55124912 | CAGCCGCTGGAAAGC[A/G]GCCTGCCATCCGGTG | 166979 |
| rs777690639 | snp | C/T | 1.65381e-05 | 0.00287555 | missense | CDC20B | GRCh38.p7 | 5:55143535 | TTTGAGGCAACACTT[C/T]CTTTCCAGTCTCTGT | 166979 |
| rs777766610 | snp | C/T | | | downstream-variant-500B | CDC20B | GRCh38.p7 | 5:55112739 | CCCTGGTATATAATA[C/T]TCTACTTTTGAATTC | 166979 |
| rs777780543 | snp | A/G | 1.78477e-05 | 0.00298723 | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164259 | CAGAGAAATGTCTCC[A/G]TGAGGGTTTGGTCTC | 166979 |
| rs777780558 | snp | A/G | 3.32e-05 | 0.00407417 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55140390 | GTTCTGGGTTACAAA[A/G]AGTTGTTTTAGGCAT | 166979 |
| rs777807464 | snp | A/G | 1.65176e-05 | 0.00287376 | intron-variant | CDC20B | GRCh38.p7 | 5:55114324 | CCCCTGTGGCCTGGG[A/G]GAAGAAGGAAAGACA | 166979 |
| rs777830348 | snp | G/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55118488 | TGGTAAGTACATTCT[G/T]TATTCTAAGCATCAG | 166979 |
| rs777918681 | in-del | -/AAA | | | intron-variant, utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55137178 | GAGACTCTGTCTCAA[-/AAA]AAAAAAAAAAAAAAA | 166979 |
| rs777923604 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55167851 | GCTGGGCAACAGAGC[A/G]AGACCCCATCTCTAC | 166979 |
| rs777978428 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55149857 | GGTTATTTTTGGCCA[A/G]GTGCAGTGGCTCACA | 166979 |
| rs778012905 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55125818 | ATTAACAATATGGGC[C/T]CTGGAGCCAGACCAG | 166979 |
| rs778042202 | snp | C/T | 1.67736e-05 | 0.00289595 | intron-variant, upstream-variant-2KB, nc-transcript-variant | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170707 | ACTTGACCCAAGCAG[C/T]CAGCTAACAATACAC | 166979 |
| rs778056521 | snp | C/T | 1.68644e-05 | 0.00290378 | intron-variant | CDC20B | GRCh38.p7 | 5:55124799 | AATCTATTGGGTTTC[C/T]TACCTTGACTGCCGT | 166979 |
| rs778168504 | snp | A/C/T | 3.29572e-05 | 0.00405928 | missense, stop-gained | CDC20B | GRCh38.p7 | 5:55146682 | CTGATCCGGAAGCTT[A/C/T]TGGGAGGTAGGTGGT | 166979 |
| rs778186791 | snp | A/G | 4.94809e-05 | 0.00497373 | missense | CDC20B | GRCh38.p7 | 5:55127273 | TGCTGAGGATAAAGT[A/G]ATTCCAGCTCAGAGC | 166979 |
| rs778214767 | in-del | -/ATTCCTAAA | | | intron-variant | CDC20B | GRCh38.p7 | 5:55141983 | TTAGTATAAAATAAT[-/ATTCCTAAA]ATGGCCTGCTCATCA | 166979 |
| rs778236217 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55129441 | TGAGGACAGGCCCCA[C/T]TGATGGAGTGCCAGC | 166979 |
| rs778279624 | snp | C/G | 1.64738e-05 | 0.00286995 | missense | CDC20B | GRCh38.p7 | 5:55146751 | TAGTTTGACTTTGCT[C/G]CCACCTTGTGGTAAT | 166979 |
| rs778289216 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55145594 | CTGGCAGGTTGATCA[C/T]GGATCCTGCCCATCA | 166979 |
| rs778296679 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55135465 | GCTTTTAAGAAAATA[C/T]CATTCTAAGGAAAAG | 166979 |
| rs778334368 | snp | A/G | 1.64738e-05 | 0.00286995 | intron-variant, upstream-variant-2KB | CDC20B, MIR449A, MIR449B, MIR449C | GRCh38.p7 | 5:55172575 | AGAGAACAAGAACAA[A/G]CCCTGGACTCACGTT | 166979 |
| rs778456545 | snp | A/G | 3.29522e-05 | 0.00405894 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55124899 | CAGTCCATCACTGCA[A/G]CCGCTGGAAAGCAGC | 166979 |
| rs778464071 | in-del | -/ACTC | 3.91474e-05 | 0.00442404 | intron-variant, upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55172932 | GCAGAAAAGGGTGTT[-/ACTC]ACCCACAGCATCTCC | 166979 |
| rs778483388 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55122666 | TAATAAAAGGTGTTA[A/G]CGCTTTCACCTTGCT | 166979 |
| rs778490787 | snp | A/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55151059 | CCACTCGAACTTTCA[A/T]TTCCCCACTTTTTTA | 166979 |
| rs778523708 | snp | G/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55148308 | AACACTGGCATACAC[G/T]GCTGTGGAGGTTAAA | 166979 |
| rs778527401 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55132401 | ATCCTCTTTCAACTA[C/T]CAGCATTCGTTTCAA | 166979 |
| rs778548875 | snp | G/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55154203 | GGGTGGAAACCTGGG[G/T]TGCTTAGTCTAGGAG | 166979 |
| rs778605471 | snp | A/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55157869 | CTCTCTTTCCACCTC[A/T]AAACACAGTTATAAT | 166979 |
| rs778633084 | snp | A/T | 1.64833e-05 | 0.00287078 | intron-variant, upstream-variant-2KB | CDC20B, MIR449B, MIR449C | GRCh38.p7 | 5:55172671 | AAAACACAGATAACA[A/T]ATTGAGGGAGAAACT | 166979 |
| rs778784440 | snp | C/T | 4.95193e-05 | 0.00497566 | splice-acceptor-variant | CDC20B | GRCh38.p7 | 5:55114319 | CTCTGCCCCTGTGGC[C/T]TGGGGGAAGAAGGAA | 166979 |
| rs778802238 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55115060 | ACATATCCCAGCCTT[C/T]CCCCAGAAGTATCCC | 166979 |
| rs778920651 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55125615 | GTGGATAATGTCTCC[A/C]TTCATGCTCAGTGAT | 166979 |
| rs778933821 | snp | A/G | 1.68187e-05 | 0.00289984 | intron-variant | CDC20B | GRCh38.p7 | 5:55140290 | AGGAGCGCAGGAAAG[A/G]AGGACAATGTCTTGA | 166979 |
| rs778966002 | snp | C/T | 1.66192e-05 | 0.00288259 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55114245 | CCATACAGAGGCCGT[C/T]CCATCAGCTGCAGCA | 166979 |
| rs778973531 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55124646 | AGTGGAAAGTATAAA[C/T]AGGGTTGTCTTTCAG | 166979 |
| rs778985783 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55150096 | GAGATCGCACCATTG[C/T]ACTCCAGCCTGGGCA | 166979 |
| rs779118034 | snp | A/G | | | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55161600 | ATGTCCCTTCCCGTC[A/G]TTATAGCCACACAGC | 166979 |
| rs779120759 | in-del | -/ATAAC | | | intron-variant | CDC20B | GRCh38.p7 | 5:55117420 | ATGTACTACATAACT[-/ATAAC]ATAAGTTTCATAAAA | 166979 |
| rs779218788 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55139097 | TCATCATGAAATCTT[A/G]GAACACTGGTGATAA | 166979 |
| rs779261608 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55155263 | AGGGGTTAAAAATAA[A/G]GTCAGGAAGTAGCAG | 166979 |
| rs779344419 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55148960 | GGCTCACCTGTCTGA[C/T]CCCAGAGTCCAGGCT | 166979 |
| rs779392014 | snp | G/T | 1.64773e-05 | 0.00287026 | intron-variant, synonymous-codon | CDC20B | GRCh38.p7 | 5:55120506 | ATCCTTCATTCCTCC[G/T]CCAATGGCAAGGACC | 166979 |
| rs779419262 | snp | G/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55124426 | AAATGAAGTCTGAAG[G/T]AAGAATGAAACCAGA | 166979 |
| rs779429211 | snp | G/T | 1.65433e-05 | 0.002876 | intron-variant, nc-transcript-variant, downstream-variant-500B | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170603 | CAGCTAACAATACAC[G/T]GCCAGCTCATCACAC | 166979 |
| rs779457314 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55156642 | GCACTTTGTGAGGCC[A/G]AGGCGGGCAGCTCAC | 166979 |
| rs779478947 | snp | A/G | 1.64841e-05 | 0.00287085 | intron-variant | CDC20B | GRCh38.p7 | 5:55120389 | ACAAGATTCCAGAAG[A/G]TCAAAATGAAGATGA | 166979 |
| rs779508666 | snp | C/T | | | intron-variant, upstream-variant-2KB | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170843 | ATTAAAGAAAACTTA[C/T]ACACAAAATGTATTA | 166979 |
| rs779513236 | snp | C/T | 1.65411e-05 | 0.00287581 | missense | CDC20B | GRCh38.p7 | 5:55124819 | TTGACTGCCGTAGAC[C/T]GGGTTATGACTTTCA | 166979 |
| rs779553004 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55145387 | AAAGAGTTGGCACTT[C/T]TATTAACATTTGTCT | 166979 |
| rs779555565 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55121121 | TAGTATCACACATTT[A/G]TATTGATAATTGAAA | 166979 |
| rs779587941 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55157692 | GTAACAGCATAATTT[C/T]GGCATTTTCAAATCC | 166979 |
| rs779685987 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55143831 | TCGCTCCAAAGTCCA[C/T]TGCAGAGAGCAGTAC | 166979 |
| rs779710949 | in-del | -/G | 1.65085e-05 | 0.00287297 | splice-acceptor-variant | CDC20B | GRCh38.p7 | 5:55114320 | CTGCCCCTGTGGCCT[-/G]GGGGGAAGAAGGAAA | 166979 |
| rs779718068 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55119449 | ACACATAATGTCTTG[C/T]CCTTTCAGATCGCTT | 166979 |
| rs779837009 | snp | A/G | 1.64787e-05 | 0.00287038 | intron-variant, upstream-variant-2KB | CDC20B, MIR449A, MIR449B, MIR449C | GRCh38.p7 | 5:55172539 | ACCAAGAATTCGTTT[A/G]TTCAAGATCAGAATT | 166979 |
| rs779842727 | snp | A/G | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164717 | TGGAATAAAACACAA[A/G]TGTTGAAAAATGTAA | 166979 |
| rs779884112 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55132365 | GATTCAATCATAATC[A/G]TCTGACCTACGGGCT | 166979 |
| rs779908300 | snp | A/G | 1.68043e-05 | 0.0028986 | intron-variant | CDC20B | GRCh38.p7 | 5:55133533 | ATCTTTGCAGCCTAC[A/G]AGAAACAAACACTTC | 166979 |
| rs779935490 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55129862 | GAACAAAAACATCAA[C/T]CAGAACAAAACATCA | 166979 |
| rs779946420 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55139651 | ATAGTTGTGTAGTAA[C/T]ATGATGTAAACATTA | 166979 |
| rs779955514 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55130884 | CCAGCACTTTGGGAG[A/G]CCAAGGTGGGAGGAT | 166979 |
| rs779960117 | snp | C/T | 1.65157e-05 | 0.0028736 | intron-variant | CDC20B | GRCh38.p7 | 5:55127249 | GTCTCCAACAAGACG[C/T]TTCTTACCTGCTGAG | 166979 |
| rs779967998 | snp | A/G | 1.67666e-05 | 0.00289534 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55114239 | GCAATTCCATACAGA[A/G]GCCGTCCCATCAGCT | 166979 |
| rs780053206 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55137971 | GAAGACTGAGAGGTG[A/G]GTTAGTTAAAAGACT | 166979 |
| rs780068743 | snp | A/G | 1.74231e-05 | 0.00295148 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160973 | TCACTTTCCGGTTGG[A/G]TTTTTTTCTTTTTCC | 166979 |
| rs780071001 | snp | G/T | 1.67612e-05 | 0.00289488 | intron-variant | CDC20B | GRCh38.p7 | 5:55125036 | TTGACCCACTGCGAG[G/T]TTACATAACAAAAAA | 166979 |
| rs780131080 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55123026 | AGATAACCAGACAGA[C/T]ACTATAAACAGAAAC | 166979 |
| rs780146909 | snp | A/G | 6.61824e-05 | 0.00575212 | intron-variant, nc-transcript-variant, downstream-variant-500B | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170586 | CCATTCACATATTCA[A/G]CCAGCTAACAATACA | 166979 |
| rs780160062 | snp | C/T | 1.78503e-05 | 0.00298744 | intron-variant | CDC20B | GRCh38.p7 | 5:55143695 | AAAACAAGATAATCA[C/T]TTTGATTGTAGGTCT | 166979 |
| rs780254747 | snp | G/T | | | upstream-variant-2KB | CDC20B | GRCh38.p7 | 5:55174565 | ACTATTATTGGATGA[G/T]AGTCAGATGCATTGT | 166979 |
| rs780255392 | snp | A/T | 3.29625e-05 | 0.00405958 | missense | CDC20B | GRCh38.p7 | 5:55119824 | CCACCTGACCTGGAC[A/T]CAGTGGGACAGGTCC | 166979 |
| rs780325595 | snp | G/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55152318 | CTAGGGAACAAATAC[G/T]CAGCCCTGTGCTTCC | 166979 |
| rs780368284 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55115996 | AGTTTACATTTATAA[A/C]GACAATGCAGGCCCC | 166979 |
| rs780375605 | in-del | -/C | 0.000100888 | 0.00710167 | utr-variant-5-prime, upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55173016 | CTCCGGCTGACTTCG[-/C]CCTGCCTGGCGTTTG | 166979 |
| rs780463862 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55124318 | GTCCTCCCTGGCACA[C/T]TTCCACCAGAGTTAT | 166979 |
| rs780470415 | in-del | -/T | 1.74231e-05 | 0.00295148 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160973 | CACTTTCCGGTTGGA[-/T]TTTTTTTCTTTTTCC | 166979 |
| rs780476925 | in-del | -/A | | | upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55174248 | AAGGGTCAGTGATCC[-/A]AAAAAAAAAAAAAAA | 166979 |
| rs780523800 | snp | C/T | 7.06314e-05 | 0.00594228 | intron-variant, downstream-variant-500B | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170503 | TAAACACACACTAAT[C/T]ACAGATTCAGTTACA | 166979 |
| rs780545076 | snp | A/G | 1.71997e-05 | 0.0029325 | intron-variant | CDC20B | GRCh38.p7 | 5:55128628 | CAGATCTATAAGAAA[A/G]GCACTTCAAATTAGT | 166979 |
| rs780572610 | snp | G/T | 1.67002e-05 | 0.00288961 | intron-variant | CDC20B | GRCh38.p7 | 5:55119965 | GCAATTTCTGATTCC[G/T]TATGAATATAGTTAA | 166979 |
| rs780586330 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55168046 | GTTTGGGTGGAGCTG[A/G]TATGAGGACACTCTA | 166979 |
| rs780597043 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55125473 | AAAAAGGAAATAAAT[A/G]TCTAACAGGTAGAGT | 166979 |
| rs780630617 | snp | A/G | 6.59413e-05 | 0.00574163 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55128481 | TTTTATCCAGGACAC[A/G]GAAGAGATATAGTTA | 166979 |
| rs780639277 | snp | A/G | 0.000140558 | 0.00838208 | intron-variant | CDC20B | GRCh38.p7 | 5:55137639 | CCACTAAAGTGATCT[A/G]TGGGAAGGGGAGAGA | 166979 |
| rs780717881 | snp | A/C | 1.82028e-05 | 0.0030168 | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160950 | AGAATTTTTTAAAAT[A/C]TTTTGCTTCACTTTC | 166979 |
| rs780727304 | snp | G/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55127162 | TTTTGTTTTATTTTT[G/T]ATTGGTTTAGGTTTT | 166979 |
| rs780770454 | snp | C/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55149606 | AAAGAAGCCAGACAG[C/G]AAAGGTCACATATTG | 166979 |
| rs780920729 | in-del | -/ATA | 3.49711e-05 | 0.00418143 | intron-variant | CDC20B | GRCh38.p7 | 5:55133574 | TAAGATCCTGAAAAT[-/ATA]ATATTTATTCTTGTG | 166979 |
| rs780937188 | in-del | -/A | 1.64849e-05 | 0.00287092 | frameshift-variant, intron-variant, splice-acceptor-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160328 | AAACCTAAAATCAAC[-/A]GCTTTTATGCCTTTG | 166979 |
| rs781053386 | snp | C/T | 3.29717e-05 | 0.00406015 | missense, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55160284 | TTCTATGCACAGTAA[C/T]GCTATTTCTTCTACA | 166979 |
| rs781108418 | snp | C/G/T | 4.48886e-05 | 0.00473737 | missense, upstream-variant-2KB | CDC20B, MIR449C | GRCh38.p7 | 5:55172982 | TCCGAGGCGCGGTGC[C/G/T]CTCCAGTTTCCACTC | 166979 |
| rs781150002 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55143457 | CCTTACATTTGCAAC[C/T]AAGTTGTCTCAGCTT | 166979 |
| rs781197249 | snp | G/T | 1.72199e-05 | 0.00293422 | intron-variant | CDC20B | GRCh38.p7 | 5:55143673 | TTTATCTTTGAATTT[G/T]GTTTTTAAAACAAGA | 166979 |
| rs781296729 | snp | C/T | 1.87591e-05 | 0.00306255 | intron-variant, downstream-variant-500B | CDC20B, MIR449A, MIR449B | GRCh38.p7 | 5:55170492 | GAAAGTACACATAAA[C/T]ACACACTAATTACAG | 166979 |
| rs781304235 | snp | A/G | 1.64955e-05 | 0.00287184 | missense, intron-variant | CDC20B | GRCh38.p7 | 5:55119807 | TTTGCTTACCAAAAA[A/G]CCCACCTGACCTGGA | 166979 |
| rs781318975 | snp | G/T | | | utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55112986 | CAAACAGTAATAAAA[G/T]ATTTTTTTAAACAGC | 166979 |
| rs781338578 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55151355 | TGGGCTACATTTGCA[A/G]CGGCTCCACTATGTC | 166979 |
| rs781348290 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55156568 | GATTGTGTGCAGTAT[A/G]AAGCTCTCTAAAAAC | 166979 |
| rs781348404 | snp | A/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55141817 | GGCAACAATTCATTG[A/T]TGTGGGAGCTGTTCT | 166979 |
| rs781377475 | snp | A/G | 1.64917e-05 | 0.00287151 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164138 | AAGTTCTGGAAGCCA[A/G]AGGAGCCCATTGAAG | 166979 |
| rs781445947 | snp | A/C | 6.58935e-05 | 0.00573955 | missense | CDC20B | GRCh38.p7 | 5:55146764 | CTGCCACCTTGTGGT[A/C]ATGGGGCTACTCGCA | 166979 |
| rs781459419 | snp | C/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | GPX8, CDC20B | GRCh38.p7 | 5:55164413 | AGGATTTTTTTTTAA[C/T]GTTATCTTGCTATTA | 166979 |
| rs781484481 | snp | A/G | | | intron-variant, upstream-variant-2KB, downstream-variant-500B | CDC20B, MIR449A, MIR449B, MIR449C | GRCh38.p7 | 5:55172253 | CATTTCCATTTCTTT[A/G]GGGGGCGTGCTTCTG | 166979 |
| rs781503724 | snp | G/T | 1.65111e-05 | 0.0028732 | synonymous-codon | CDC20B | GRCh38.p7 | 5:55143555 | CCAGTCTCTGTCCAT[G/T]GCATGAGGTGCCTTG | 166979 |
| rs781504477 | snp | A/G | | | upstream-variant-2KB, intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55159313 | TGAGCCACCATGCCC[A/G]GCCTCAGTTTTTTCC | 166979 |
| rs781528498 | snp | A/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55129110 | AATAAGAAACCTTTG[A/T]CTGCTAAGAGAAAAC | 166979 |
| rs781594789 | snp | G/T | | | intron-variant, utr-variant-3-prime | CDC20B | GRCh38.p7 | 5:55137498 | ACTTGGCTTATGTGG[G/T]ATCTGTTTCATAGTT | 166979 |
| rs781745363 | snp | C/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55142323 | CTCTCGATGCTATTT[C/G]ACTTCTAACTAATCA | 166979 |
| rs781761444 | snp | G/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55122950 | CAGGAAACCATAAAA[G/T]ATAATGAAATGATTA | 166979 |
| rs781769868 | snp | A/G | 1.70889e-05 | 0.00292304 | intron-variant | CDC20B | GRCh38.p7 | 5:55146867 | AGTACCTGTTTAACA[A/G]CAAAAACAGCTGTAA | 166979 |
| rs796188373 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55157398 | TCCAATGCTGTCCAG[C/T]GCACAAGTTCTCCAA | 166979 |
| rs796365599 | snp | C/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55115850 | ACTCCCAACACTCTC[C/T]TTTGTGCCTGTCCAC | 166979 |
| rs796467031 | snp | C/T | | | intron-variant | GPX8, CDC20B | GRCh38.p7 | 5:55162925 | CTGGAGTAAAAGGCC[C/T]GTATATCAATCCTGG | 166979 |
| rs796537880 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55156863 | TAGCCGACAGAGTGA[A/G]ATTCTGTCTCAAAAA | 166979 |
| rs796553863 | in-del | -/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55120966 | TATGTTCCAGGTAGT[-/G]GGTCAGATAAGAGAA | 166979 |
| rs796695610 | in-del | -/T | | | intron-variant | CDC20B | GRCh38.p7 | 5:55121592 | TACATTCTACATGTC[-/T]TTTTTTCTGACAAAT | 166979 |
| rs796727022 | in-del | -/AAG | | | upstream-variant-2KB | CDC20B | GRCh38.p7 | 5:55174786 | TTTCTTACAAGTACT[-/AAG]AATAGTGAATCATTC | 166979 |
| rs796786499 | snp | A/G | | | intron-variant | CDC20B | GRCh38.p7 | 5:55126278 | GGCCGAGGCAGGTGG[A/G]TCACAAGGTCAGGAG | 166979 |
| rs796802989 | in-del | A/TCAGGAGG | | | intron-variant | CDC20B | GRCh38.p7 | 5:55126278 | GGCCGAGGCAGGTGG[A/TCAGGAGG]TCACAAGGTCAGGAG | 166979 |
| rs796866630 | snp | A/C | | | intron-variant | CDC20B | GRCh38.p7 | 5:55138813 | TAAAAAGTTTCATAG[A/C]GAGGTTGGTGAACAG | 166979 |