SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs145431330 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KDM2A | GRCh38.p7 | 11:67166839 | TCCAGCAATTTGGAA[A/G]GCCAAGGCGGGCGGA | 22992 |
rs145470066 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67162697 | AGGCATGAGCCACCG[C/T]GCCCGGCCTGCGATT | 22992 |
rs145472106 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67217963 | GGATTACCACCAAGA[A/G]TAGTTATGATGCTGG | 22992 |
rs145490991 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67145344 | ACACACACAAAATTA[A/G]CCAGGTGTAGTTGCG | 22992 |
rs145512766 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67214652 | ACTATTTTTTTATTT[G/T]GAAGAGATGGGTTCT | 22992 |
rs145555062 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67159797 | TGAAGACAATAGTGG[A/G]AATGGATCTGTTTTT | 22992 |
rs145579580 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67178558 | ATTCTTCATTTTCTC[C/T]AGCCCCTGGCAACTA | 22992 |
rs145589452 | in-del | -/C | 0.120326 | 0.21374 | intron-variant | KDM2A | GRCh38.p7 | 11:67164681 | GCTGGAGTGTAGTGG[-/C]ACAATCTCGGCTCAC | 22992 |
rs145708524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67164977 | TTCAGCGATGAAGAC[A/G]TAGTTTTCTCTGCTT | 22992 |
rs145747026 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67132319 | TATGGAGTCTCACTG[C/T]GATGTCCAGGCTAGA | 22992 |
rs145785935 | snp | C/G | 0.00398564 | 0.0444627 | | | GRCh38.p7 | 11:67179506 | TCTAATCTCGAACTC[C/G]CGACCTCAGGTGATC | 22992 |
rs145805245 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67141030 | AAAGGTTGATAAATA[C/G]TACTCATTTAGCTTT | 22992 |
rs145805299 | snp | A/C | 0.0155059 | 0.0866749 | intron-variant | KDM2A | GRCh38.p7 | 11:67196214 | CCATGGTGCACGAGC[A/C]GGGGCTTGCAGCCCA | 22992 |
rs145823781 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67175667 | AACTTTTTGCCTATC[A/G]TATTAGAAATGTTGG | 22992 |
rs145849387 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | KDM2A | GRCh38.p7 | 11:67151673 | CCTGAAGACTTGGTA[C/T]GAAAAAAGGATTAAA | 22992 |
rs145920683 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67191786 | GGAACAGCGTAAAGG[C/T]GCCTGCTTTTACTGC | 22992 |
rs145935861 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67163508 | GCCACTTAGGCCATT[C/G]TTTTTGGGACATACA | 22992 |
rs145959444 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67233508 | AATACAAAAATTAGC[C/T]GGGTGTGGTGGCAGA | 22992 |
rs145959754 | snp | A/G | 0.000696044 | 0.0186424 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67254276 | CATCACAGATGCCAC[A/G]CTTCGCCTCATAATT | 22992 |
rs146082123 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | KDM2A | GRCh38.p7 | 11:67222961 | CACTTTGGGAGGCTA[A/G]GCAGGCAGATTACCT | 22992 |
rs146139491 | snp | C/T | 0.00934559 | 0.067716 | intron-variant | KDM2A | GRCh38.p7 | 11:67181803 | TCACATTTACTAGAG[C/T]AATTGTGTTTTCCAT | 22992 |
rs146180569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67209506 | TTTAGTGCAGTGGCA[C/T]GATCTTGGCTCACTG | 22992 |
rs146191367 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67204999 | TGAACACCTTGTTCA[A/G]TTCTTTTAGATATAT | 22992 |
rs146209718 | in-del | -/A | 0.00795532 | 0.062565 | intron-variant | KDM2A | GRCh38.p7 | 11:67195742 | AGTTATATTGTACTT[-/A]ATATTCAGTAAAGAA | 22992 |
rs146212696 | in-del | -/ATATATATATATATATATATATATATATATATA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67247039 | GTTATAAATTATTTT[lengthTooLong]TTTTTTTTTTTTTTT | 22992 |
rs146252890 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | KDM2A | GRCh38.p7 | 11:67134657 | TTACAGGTATGCGTC[A/G]CCACGCCCAGCTAAT | 22992 |
rs146254426 | in-del | -/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67169759 | TCTCTCTCTCTCTCT[-/C]TTTTTTTTTTTTTTT | 22992 |
rs146259060 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67158138 | ACCAGCAACTACGGA[C/T]CTTTTTGCTGTCTGT | 22992 |
rs146296975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67186764 | TAATTTGAGAGATCA[A/G]TACATTTAAAATAAT | 22992 |
rs146308660 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67182300 | GGAAACTTGCCTAAG[A/G]CTTGAAACTTTATAG | 22992 |
rs146326919 | in-del | -/TGC | 0.0722614 | 0.17581 | intron-variant | KDM2A | GRCh38.p7 | 11:67139694 | CAAAGGTTGCAAGGT[-/TGC]TGCTGCTATTTTTTT | 22992 |
rs146405915 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | KDM2A | GRCh38.p7 | 11:67258257 | GCTTCTAGAAATACA[A/G]CGTTTACTTCATCAA | 22992 |
rs146406620 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | KDM2A | GRCh38.p7 | 11:67137912 | AAGTGATTCTTCTGC[C/T]TCAGCCTCCTGAGTA | 22992 |
rs146441712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67155524 | GCCCAAGCTGGTTTC[A/G]AACTCTTGGCCTAAA | 22992 |
rs146455402 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | KDM2A | GRCh38.p7 | 11:67249242 | CATTAGTGATGTTGA[A/G]TGTTTGCATCTCTGC | 22992 |
rs146469240 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67252054 | GTAGATTTGTAGACT[A/G]CAGTGGAAAGCCAGG | 22992 |
rs146485612 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | KDM2A | GRCh38.p7 | 11:67173079 | CACTGCAGCTTGGAC[C/T]TCTCCAGGCTTAGGA | 22992 |
rs146517317 | in-del | -/AA | 0.0115144 | 0.0749975 | intron-variant | KDM2A | GRCh38.p7 | 11:67241503 | AGAATGAAAATACAT[-/AA]AAGTCCTGGTCTCCG | 22992 |
rs146532672 | in-del | -/GTGTGTGTGTGT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67152906 | GATTACAGTGCCAGA[-/GTGTGTGTGTGT]GTGTGTGTGTGTGTG | 22992 |
rs146562453 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67134124 | CTTGGATTACCAGGA[A/G]GACTGGGGGAAAGAT | 22992 |
rs146578499 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67217300 | TCTCCAAATCCAAAA[A/G]TCATTTTGTTTGCTT | 22992 |
rs146606114 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67150251 | AAATTCACTGCCTCT[C/T]AGTTTACCTCAAATT | 22992 |
rs146650294 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67153315 | CATGTTTACAAGGAC[A/G]TGTAATTGGAAAGGT | 22992 |
rs146722025 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67131844 | TCATGAACTTTGAAC[G/T]TATTGCACTTGATCT | 22992 |
rs146738671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67213217 | CTCCATTCACATTAT[A/G]AGGGAAGTAAGTGAT | 22992 |
rs146793443 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67130699 | TGTTTATCTCACTTT[C/T]GGAATAATACTTTAT | 22992 |
rs146804238 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67177717 | TAAGAAAAAAAAAAG[A/T]AGAAGGAATGCATGC | 22992 |
rs146845597 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67196167 | TAACAAGACATAATC[C/T]ACTACAGTGAAACTT | 22992 |
rs146857447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67190470 | AAATAAAAAGGATTG[C/T]AAGAGAATACTATGC | 22992 |
rs146865546 | in-del | -/GTGTGTGTGTGTGT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67152906 | GATTACAGTGCCAGA[-/GTGTGTGTGTGTGT]GTGTGTGTGTGTGTG | 22992 |
rs146870134 | snp | A/G | 0.00018439 | 0.00960004 | intron-variant | KDM2A | GRCh38.p7 | 11:67250807 | ATAAATGGTGAGCAG[A/G]GATTCAGGGGGTCAG | 22992 |
rs146934712 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | KDM2A | GRCh38.p7 | 11:67225007 | CCACCACGCTAATTT[G/T]TGTATTTCTAGTAGA | 22992 |
rs146969720 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67132855 | CTGGAGTTGGGGCCT[A/C]GCAATCTGTGTTTTA | 22992 |
rs147041045 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KDM2A | GRCh38.p7 | 11:67202783 | TTCGTCTCAAAAAAA[A/G]AAAAGAAAAGAAATT | 22992 |
rs147046284 | in-del | -/GT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67242270 | TAGCAGACTCTGTGG[-/GT]GTGTGTATGTGTGTG | 22992 |
rs147050590 | snp | A/C | 0.0337553 | 0.125452 | intron-variant | KDM2A | GRCh38.p7 | 11:67198535 | AGACCACGGTGAAAT[A/C]CCATCTCTACTAAAA | 22992 |
rs147144790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67128126 | TCTTACCTCAGCCTC[C/T]TGAGTGGCTGGTACC | 22992 |
rs147199593 | snp | C/G | 1.67517e-05 | 0.00289406 | intron-variant | KDM2A | GRCh38.p7 | 11:67253418 | GTATGCTGGGAAACA[C/G]TGTATTATTACATGT | 22992 |
rs147200066 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | KDM2A | GRCh38.p7 | 11:67187886 | GGCCCTAAAACAGAC[C/G]TTAAATCAAAGAATG | 22992 |
rs147210181 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67245728 | TTTCCCCTCTTCAGG[C/T]AGATTAGAAAGGACC | 22992 |
rs147294578 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67168804 | GTTGATTTTTTGGAT[A/G]TGTATGCATTCATAT | 22992 |
rs147314593 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | KDM2A | GRCh38.p7 | 11:67216448 | TTATCTTTATTCATT[C/T]AGTTATATTCCAGCT | 22992 |
rs147400200 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67146869 | TTCGTGGATTTTATC[G/T]ATTTATTATTCCTTA | 22992 |
rs147402314 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67243349 | AAATTGTGCATTTGT[A/G]CATCCGCTTCTATCC | 22992 |
rs147412093 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67236616 | CTGTTTTCTCTAAAC[A/G]TTTTGATAAGCCTGC | 22992 |
rs147426949 | in-del | -/TTATT | 0.031825 | 0.122064 | intron-variant | KDM2A | GRCh38.p7 | 11:67151355 | CACATATTTTATTTA[-/TTATT]TTATTTTATTTTTAA | 22992 |
rs147507210 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67215625 | GCATACCATAGCACA[C/T]AACCACACAGTTAAA | 22992 |
rs147516540 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67124840 | ACACATCATCTATTT[A/G]GAGAGAACTTTCTTT | 22992 |
rs147516996 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | KDM2A | GRCh38.p7 | 11:67210545 | GTGACATCATTTTAT[A/G]AAAATTAGAAAAATA | 22992 |
rs147571357 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | KDM2A | GRCh38.p7 | 11:67231030 | AATATGATCGCAGCT[C/G]ACTGCAGCCTCAACC | 22992 |
rs147632680 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67184556 | TTGCTTGAACCGGGA[C/G]GCAGAGGTTGCAGTG | 22992 |
rs147642228 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67236958 | GCTAAGAAATAGGAA[A/G]TAAGTGCAGTCCAGG | 22992 |
rs147666031 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67156899 | TCTCTCAAAAAGAAA[A/G]TATGAAATAGGAGCT | 22992 |
rs147666119 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | KDM2A | GRCh38.p7 | 11:67211574 | AGCCATGATCACACC[A/G]CTGCACTCCAGCCTG | 22992 |
rs147675628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206625 | CCTGTAGTCCCAGCT[A/G]CTGTGGAGGTTGAGG | 22992 |
rs147734085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67160276 | ATTATTGATGTCTCT[A/G]GGTATGCTGTTGCCA | 22992 |
rs147735910 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67125943 | GCAAGGCTTCACCTC[-/A]AAAAAAAAAAAAAAA | 22992 |
rs147770696 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67134878 | CCACATCATGCTTTG[C/G]AAAAGTAAGCATGAA | 22992 |
rs147839805 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67139994 | TAGGCGTGAGCCACC[A/G]CACCTGGCCTACTCC | 22992 |
rs147931180 | in-del | -/TG | | | intron-variant | KDM2A | GRCh38.p7 | 11:67172617 | ATTAGCTCTTATAGT[-/TG]TGTGTGTGTGTGTGT | 22992 |
rs147946478 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67120265 | GCACGGTTTCCCTCC[A/C/T]GACTTCGGGCCAGGG | 22992 |
rs147948446 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67205862 | TAGCTTATATTTTAC[C/T]TCTGCATGGAATTGT | 22992 |
rs147989582 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67123480 | ATTGTATCGTTGGGA[C/T]TTATTTTTATTTTTA | 22992 |
rs147998889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67136247 | CCATTTTAAAGTTTT[A/G]GAAACAGATCCAAAG | 22992 |
rs148009033 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67186301 | AGTAAAATTATGAAC[C/G]AATTTCTCATCAGAA | 22992 |
rs148044145 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67204408 | TGTCTTGGTGAATTT[G/T]TCTAATCTGTATATT | 22992 |
rs148097849 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67251800 | AGTCTCTAAATAGAC[C/G]CTATTCTTTGCAAAC | 22992 |
rs148126350 | in-del | -/AAAG | 0.175254 | 0.238565 | intron-variant | KDM2A | GRCh38.p7 | 11:67196908 | TTACAAGTTGAAAAA[-/AAAG]AAAATAGACTCCTGG | 22992 |
rs148167671 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67191906 | AGTCACCTCTGTTGG[C/T]AGATGATATGACTTT | 22992 |
rs148205036 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KDM2A | GRCh38.p7 | 11:67164356 | GATTTCTTAATGTTT[C/T]AGATGGGATACTTAA | 22992 |
rs148254964 | in-del | -/TTA | 0.0752113 | 0.178743 | intron-variant | KDM2A | GRCh38.p7 | 11:67237442 | TTTTTAAATTTTTCT[-/TTA]TTATTATTATTATCA | 22992 |
rs148257722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67157930 | CCCCATCGCAAAAGA[A/G]AGAGAGAGATACATT | 22992 |
rs148309751 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67198097 | GGCTAAGGAGGAAGA[C/G]GTGGGATTGCTTTTG | 22992 |
rs148350087 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67140768 | AAAAAAAAAAAGTTA[C/T]AAGTATACTTTTGAT | 22992 |
rs148377589 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67146449 | AGAAGTTAAAACATT[C/T]AATGAATTCAGTTGA | 22992 |
rs148391343 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67254104 | CTACTTAACCCCTTC[A/G]AGGGGGCCTGGCCAG | 22992 |
rs148485228 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | KDM2A | GRCh38.p7 | 11:67194342 | ATTCCCAGATCTAGC[A/G]TCTTTCAAAACATCT | 22992 |
rs148508658 | in-del | -/CAA | 0.455977 | 0.141681 | intron-variant | KDM2A | GRCh38.p7 | 11:67233652 | AGTGAAACCCTGTCT[-/CAA]CAACAACAACAACAA | 22992 |
rs148528265 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67182480 | ATTGTGGTCCTGAGA[C/T]ACCTCAGCATCCTTA | 22992 |
rs148531929 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67216997 | CGCCTGTAATCCAAC[A/C]CTTTGGGAGGCCAAG | 22992 |
rs148537731 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67235494 | TTTTAGTAGAGACTG[C/G]GCTTCTTCATGTTGT | 22992 |
rs148571635 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KDM2A | GRCh38.p7 | 11:67159753 | GAGATTTCTACTCTC[A/G]CATACCTTACCTTTT | 22992 |
rs148580889 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67176858 | GGACTGAAAGTTGCT[C/T]TAAGTGAGTCAGTGA | 22992 |
rs148642951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67155592 | TACAGGAGTGAGCCA[C/T]TGCACTGGCTTGGTT | 22992 |
rs148692966 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67148975 | ACTATTTATAGGTTT[A/G]GGTTGTTATAACATG | 22992 |
rs148696761 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67246273 | CAGCCCTTGATTCAT[A/T]TATGTACAATGTGTC | 22992 |
rs148716282 | in-del | -/TTCC | 0.0726307 | 0.176182 | intron-variant | KDM2A | GRCh38.p7 | 11:67192193 | CATTTTCAATCCCTT[-/TTCC]TTCCTCCTCTCTCCA | 22992 |
rs148738507 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67138696 | TGAGGCAGAAGAATT[G/T]CTTGAACCTGGGAGG | 22992 |
rs148758533 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67205560 | ACCCTCCCGAGTAGC[A/C]GGGATTACGGGCACG | 22992 |
rs148791387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67221230 | TAGAATATTTGGGGG[C/T]TGTGATGTTTGTAAG | 22992 |
rs148848855 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185737 | AGAGATAATTAGGCT[A/G]CAGGGACTCCACTCT | 22992 |
rs148858316 | snp | A/G | | | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67239407 | GTTTTAGATGTAGTT[A/G]ATGTTAGCCGTATTT | 22992 |
rs148898864 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67178906 | GTTTTCAGTTCTTTG[C/G]GTTATATACCTAGGA | 22992 |
rs148917213 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | KDM2A | GRCh38.p7 | 11:67165049 | GGAAAGAGGTCTTGC[C/T]AGGACTGTAATGTAA | 22992 |
rs149013344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67152145 | CATAGTGAAACCCTG[C/T]GTCTATTAAAAATAC | 22992 |
rs149014665 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67251056 | ATGGGGAGGGAGACT[C/G]ATTTGCGGGATAGAT | 22992 |
rs149054896 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67140124 | CCAACACTTTGGGAG[A/G]CTAAGGCAGGAGGAG | 22992 |
rs149064277 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | KDM2A | GRCh38.p7 | 11:67190287 | TGGTGGTACATGCCT[A/G]TAATCCCAGCTACTC | 22992 |
rs149069708 | in-del | -/TGTG | | | intron-variant | KDM2A | GRCh38.p7 | 11:67201219 | ATATATATATATATA[-/TGTG]TGTGTGTGTGTGTAT | 22992 |
rs149108389 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67134433 | GTAAAGGGAAATACC[C/T]AGTAGATAGGTTGCA | 22992 |
rs149129143 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67258067 | TAAAAAAATAAAAAG[G/T]CTTTAAAAACAAAAA | 22992 |
rs149151088 | snp | A/G | 0.175897 | 0.238765 | intron-variant | KDM2A | GRCh38.p7 | 11:67125736 | CTAAGCAGAGATTGC[A/G]CCACTGCACTCCAGC | 22992 |
rs149225961 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67196985 | TCAGTCATCAGTCTT[C/T]GGTTTTCTTCCCACT | 22992 |
rs149233515 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67167291 | TGTTGTTGTTGCAGA[A/G]TTGTGATGATATCAT | 22992 |
rs149329687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67123449 | TTGTAGAAATTAAGC[A/G]TATCTGTAGTAGAAT | 22992 |
rs149350681 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | KDM2A | GRCh38.p7 | 11:67234268 | ACAGCTGGGGACTTT[C/G]AAGTGCTAGAAAACT | 22992 |
rs149382734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67157702 | GTGAGCTGAGATGGC[A/G]CCACTGCACTCCAGC | 22992 |
rs149394803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67176408 | TAGATTTGATGTTCT[C/T]AGCACAGATAAAGGT | 22992 |
rs149404968 | snp | A/G | 0.119978 | 0.213528 | intron-variant | KDM2A | GRCh38.p7 | 11:67225875 | TTCGAGACCAGCCTG[A/G]CCAAGATGGTGAAAC | 22992 |
rs149448996 | snp | A/C | 0.0248432 | 0.108648 | intron-variant | KDM2A | GRCh38.p7 | 11:67215004 | CAGACAACACCTTTT[A/C]TTGGATTAAAAAATA | 22992 |
rs149587453 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67187106 | ATTTAACTTCAGGAT[A/G]TTAGATGTAATCCCT | 22992 |
rs149589450 | in-del | -/A | 0.162253 | 0.234095 | intron-variant | KDM2A | GRCh38.p7 | 11:67208147 | ATAATTTGTATTTTT[-/A]TAAAGATATATTGAT | 22992 |
rs149597477 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67242519 | AAAAGTGAAGAAGCA[A/G]TAATAAAGTTTTACT | 22992 |
rs149604387 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | KDM2A | GRCh38.p7 | 11:67132964 | ATAGAAGCAAGACAC[A/G]TTGGCAGTGAAGGAC | 22992 |
rs149640085 | snp | G/T | 0.00935673 | 0.0677556 | intron-variant | KDM2A | GRCh38.p7 | 11:67181802 | CTCACATTTACTAGA[G/T]CAATTGTGTTTTCCA | 22992 |
rs149667397 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67144881 | TTTTATTTTTATTTA[C/T]ATTTTTGAGACAGAG | 22992 |
rs149671013 | snp | C/G | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67238505 | GAGTCTTAAGATACA[C/G]TGTCCGGGAGAAGTT | 22992 |
rs149702401 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67159447 | CTGGAAGTTGGATCT[A/G]GAAGATTAGATTCAT | 22992 |
rs149711191 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67178465 | TATATTCACAGGGTC[A/G]TACAAATACCACTAT | 22992 |
rs149762395 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | KDM2A | GRCh38.p7 | 11:67130659 | GGGTAACGGACACTC[C/T]TAATTAGGTTTCATT | 22992 |
rs149818247 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67210137 | TTGGGGAGGCCGAAG[A/G]CAGACAGATTGCTTG | 22992 |
rs149818542 | in-del | -/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67152282 | GCACCACTGCACTCC[-/C]AGCCTGGGTGATGGA | 22992 |
rs149864922 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67202396 | ATGGGTAAAATGATA[C/T]CAAACAGCATTGCAT | 22992 |
rs149878670 | in-del | -/GGAG | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67256211 | TCTGCGCGTGTGTGT[-/GGAG]GGAGGGAGGGAGGGG | 22992 |
rs149915848 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67205325 | TAGTAATATATATAT[A/T]CTGCCTTGTCTATTT | 22992 |
rs149924082 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67134279 | CATTTCTGATGGTCA[A/G]ACTGGGGTAGTGCTA | 22992 |
rs149955931 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | KDM2A | GRCh38.p7 | 11:67147986 | CCGGCCCTCATTAGA[A/G]AGTCTTATAGCAAAT | 22992 |
rs149976276 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | KDM2A | GRCh38.p7 | 11:67171793 | AGAGTGCTGGGATTA[C/T]AGGCATGTGCCACTG | 22992 |
rs150071315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67125507 | CTGGGTGTGGTGGCT[C/T]ACACCTGAAATCCCA | 22992 |
rs150073914 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67256396 | AATTTCTTTTGGGTC[A/T]ATATTTTTAAGTGTG | 22992 |
rs150082986 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KDM2A | GRCh38.p7 | 11:67218236 | CTAGGGAATGGCTGT[A/G]AAGGCTGGAGTGCTC | 22992 |
rs150178798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67167137 | TAGCACCCAAGGAGA[C/T]AAATATATGCATATT | 22992 |
rs150198893 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67192301 | AAATGGCATCATAGT[G/T]TACAAATCATTCTGC | 22992 |
rs150230029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67121685 | AATACATCTGATTAC[A/G]TTAGATTAGAATATA | 22992 |
rs150230968 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206889 | TTCGTGTCCATCCTG[A/G]TGTCTTTATCATTCT | 22992 |
rs150239391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67136295 | GATTATCCAGTTAAG[A/G]GACAGAGCCAGGATT | 22992 |
rs150291363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67174025 | CACTTTGGGAGGCCA[C/T]GGCAGGCAAATCACC | 22992 |
rs150386356 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67127537 | CGCATGTTCAATCCT[A/G]TTAACCTGTCTTACA | 22992 |
rs150408128 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67241626 | AGTTACCATCCTGTA[C/T]ATACATACCTAGGGT | 22992 |
rs150442151 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67161606 | CTCAAATTTCATTTA[A/C]AAAATACACACTGTT | 22992 |
rs150452553 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67180373 | TTTGCATGCACTTAT[C/G]CCCCAGTCCTCCCAC | 22992 |
rs150462495 | snp | A/C | 0.0729998 | 0.176553 | intron-variant | KDM2A | GRCh38.p7 | 11:67232772 | GAGTGCAATGGCAAG[A/C]TCTCGGCTCACTGCA | 22992 |
rs150525864 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67209935 | CATGGTGGCATGCAC[C/G]TGTAGTCCTGGTTAC | 22992 |
rs150547728 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | KDM2A | GRCh38.p7 | 11:67124034 | TTTGAGACTGAGTCT[C/T]GCTCTGTTGCCCAGG | 22992 |
rs150560859 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67229036 | CCGGTTGTCTAATGC[A/G]TTTTATTGTATAAAG | 22992 |
rs150566463 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67154596 | TGTCACACACCTGGC[A/T]AATTTTTTCTTTTTT | 22992 |
rs150611220 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67141971 | TTTAATATTCTCCAA[G/T]TCCATCCATGTTCCG | 22992 |
rs150613065 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | KDM2A | GRCh38.p7 | 11:67177191 | GAATCACTTGAACCC[A/G]GGAGGTGGAGGTTGC | 22992 |
rs150681011 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67130388 | CACCTCCAGTGATCC[A/G]CCCACTTCGGCCTCC | 22992 |
rs150722876 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB, missense | KDM2A, LOC107984341 | GRCh38.p7 | 11:67118259 | CCCCCGGGCCGTCGC[A/G]GAGACCGCTTCTGCG | 22992 |
rs150731998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67164467 | AGTGTTGATCTTGCT[A/G]TTGGCCTTTTTTTGT | 22992 |
rs150769005 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67174704 | ATGGTGAATATTTTT[-/T]AAGACATTTAAAATT | 22992 |
rs150776762 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67199294 | GCCTCTTAAGTGTTC[A/G]AGTGAAAGGAAGAGT | 22992 |
rs150823978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67221920 | AGCCTGGGTGGAAGA[A/G]TGAGACACAGTCTGT | 22992 |
rs150894253 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67170335 | ACAAATATCAGAAAT[C/T]TCTTACCCCAGGGAA | 22992 |
rs150928217 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | KDM2A | GRCh38.p7 | 11:67144421 | CCATGCCTGGCTAAT[A/T]TTGTATTTTTAGTAG | 22992 |
rs150938270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67195047 | CAGTGTAGAATATAT[A/G]CAATTCTGGACCTAG | 22992 |
rs150966289 | in-del | -/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67182530 | TAAAATTGAATAAGT[-/C]TTTTTTTTTTTTTTT | 22992 |
rs150998939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67132140 | CATAAGCTTTATACT[A/G]CTACTATAAGGCCTA | 22992 |
rs151003407 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KDM2A | GRCh38.p7 | 11:67218060 | TTGTTTTCAGTTTGA[A/G]AAGGCAGTGGTTTTC | 22992 |
rs151044827 | snp | C/T | 1.65971e-05 | 0.00288067 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | KDM2A | GRCh38.p7 | 11:67121325 | GTGAGAGATGGAACC[C/T]GAAGAAGAAAGGATT | 22992 |
rs151054205 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67166002 | ACTTAACAGTTGCAT[C/T]AATTATAAAAGGTGG | 22992 |
rs151099429 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67201918 | TCTGATCTTGCCACT[C/G]TATTCCAGCCTGGGC | 22992 |
rs151143145 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | KDM2A | GRCh38.p7 | 11:67188684 | TAGTCTAAGCTACTC[A/G]GGAAGCTGAGGTGGG | 22992 |
rs151152834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67247704 | TGCTGGGATTACAGG[C/T]GTGAGCCACCATGCC | 22992 |
rs151212300 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KDM2A | GRCh38.p7 | 11:67173423 | CACCGTTCTTGGCCT[A/G]ATTTTTGTATTTTTA | 22992 |
rs151222310 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67223999 | CCACATAAGAAACCA[A/G]AATCAGGGTCTGGCT | 22992 |
rs151255255 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | KDM2A | GRCh38.p7 | 11:67161162 | AGGCTAGGAGTTTGA[G/T]ACTAACTTGAGAACG | 22992 |
rs151265238 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67212414 | GAGATTATTTAGTGC[C/T]GCCATTCCAGCAATA | 22992 |
rs151303515 | in-del | -/TATC | 0.108755 | 0.206276 | intron-variant | KDM2A | GRCh38.p7 | 11:67203464 | ATTATATTTATTAAT[-/TATC]TATTAATAATTATTA | 22992 |
rs151309404 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255176 | CCTCTCTGCTCTCCT[A/G]TCCCTTGAGCCCTTC | 22992 |
rs180677058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67212990 | CCAGGGCTTATTCAA[C/T]GTTCTGGGACCGGCG | 22992 |
rs180690687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67253798 | AGATAACTACCTACA[A/G]ACAATGGAGTAAGTC | 22992 |
rs180696037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67230556 | GCTTGAGCCCAGGAG[A/G]TTGAGGCTGCAGTGA | 22992 |
rs180720172 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67184998 | TGGCCCATTCAAAGG[A/C/G]AAAAAATCAACAGAA | 22992 |
rs180728786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67166208 | TTTTTTTTTTTTGAG[A/G]CAGTCTCACTCTATC | 22992 |
rs180739680 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67150650 | GAGGGATCTAAGAGT[G/T]GGAGGATATGTCAGA | 22992 |
rs180742651 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67239411 | TAGATGTAGTTGATG[G/T]TAGCCGTATTTTATT | 22992 |
rs180745348 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67203207 | AAAGTATTTTTAAAT[A/G]AAAGTATGTACCTTG | 22992 |
rs180748861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67218695 | CTGCAACCTCCACCT[C/T]CCAGGTCCCAGTTCA | 22992 |
rs180759245 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67194614 | ATAGGCACCCAATAC[A/G]TATTGGTGATTGCCT | 22992 |
rs180841112 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67125490 | AAATAACTAGTTAAG[G/T]ACTGGGTGTGGTGGC | 22992 |
rs180842695 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | KDM2A | GRCh38.p7 | 11:67145358 | AGCCAGGTGTAGTTG[C/T]GTGTGCCTGTAATCC | 22992 |
rs180864972 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67179430 | AGGCATGTGCCACTA[C/T]GCCCAGCTTATTTTG | 22992 |
rs180874533 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67198505 | AGGCGGGCGGATCTC[A/G]AGGTCAGGAGATCGA | 22992 |
rs180884392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67162298 | ATAAGGTCAGGTAAA[A/G]TTCATTTAATTCTTA | 22992 |
rs180984294 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | KDM2A | GRCh38.p7 | 11:67131977 | TTTTTCTCTGTCTGT[C/G]AGTACTTGGTAAAAA | 22992 |
rs181236055 | snp | C/T | 0.000628022 | 0.0177092 | intron-variant | KDM2A | GRCh38.p7 | 11:67215474 | CCCTGCATCTTCCTC[C/T]GTGTGCTGTGGGAGA | 22992 |
rs181264445 | snp | C/T | | | downstream-variant-500B | KDM2A | GRCh38.p7 | 11:67258129 | GAGCAAGTCAGAAGG[C/T]TAAGGCCACGGAGCC | 22992 |
rs181280221 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67246746 | AAAATCATGACTGTC[A/G]CCTGACAGTGATAAT | 22992 |
rs181291471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67202117 | CAAATGTGGTGAAAA[C/T]AGTGAGAGAGCTAGA | 22992 |
rs181305463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67234146 | TATTTGATCAGTTAT[A/G]CTAAATCTCAGAAAA | 22992 |
rs181317651 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67128081 | GTGCAATGGCACTAC[C/G]ACTGCAGCATCAGCC | 22992 |
rs181346818 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67184748 | AAGCGACTGCATATG[C/T]ACATGGACGGTCAGG | 22992 |
rs181356248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67149761 | GTTTTCTCTTTTTTG[C/T]CTAGGCTGGAGTGCG | 22992 |
rs181380310 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67230042 | TTAGCTAGACGTGGT[A/G]GCAGGCACCTGTAGT | 22992 |
rs181390710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67253301 | ATGTAGTATAGGATA[C/T]CATGGAAATCTTTGA | 22992 |
rs181394424 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67173573 | GTTTTTGTATTTTTA[A/G]AAGAGACAGGTTTTG | 22992 |
rs181415750 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | KDM2A | GRCh38.p7 | 11:67212032 | CAGGCAAAGTAGCAC[A/G]TGCCTTTAGTCCCAG | 22992 |
rs181439619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67244935 | AGCTTGCAGTGAGCC[A/G]AGATCATGCCACTGT | 22992 |
rs181443844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67140398 | GTTTTATACAAAGAA[C/T]ATAGGTCGGAAGACC | 22992 |
rs181478222 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67130141 | CTAATTTTTTTTTTT[C/T]TCTTGCACCAAAGCT | 22992 |
rs181483666 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67155908 | GGTGTGAGCCACTGC[A/G]CCTGGCCGGTTTTTA | 22992 |
rs181500568 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67193854 | CAACAGAGTGAGACC[C/G]CATCTCAATACATAC | 22992 |
rs181501132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67133185 | GCTCAGTGCAATCTC[C/T]GCCTTCAGGGTTCAA | 22992 |
rs181513845 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67257937 | TCTTTCCTCTGACAC[A/G]TGGGAATGGGTGATA | 22992 |
rs181514032 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67170046 | CTGGCGTGAGTCACC[A/G]TGCCTGGCCCACAGT | 22992 |
rs181516665 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | KDM2A | GRCh38.p7 | 11:67197784 | AAGTGCTTAGAACAG[G/T]GTCTGGCATATACAG | 22992 |
rs181517217 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67207259 | TTAGGATTAAATGAG[A/G]CATTAGATAAAAGAG | 22992 |
rs181519742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67189561 | AGACCTTATCTCGGC[C/T]GGGCGAGGTGGCTCA | 22992 |
rs181524967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67161982 | TATTTATATTATGCT[C/T]TTAGTAGTTGTCTTT | 22992 |
rs181533257 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67233373 | AAAATACAAAAAAAG[G/T]CTCAGTGCGATGTCT | 22992 |
rs181590337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67159790 | CAGAGTTTGAAGACA[A/G]TAGTGGGAATGGATC | 22992 |
rs181593894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67122083 | GCCAAAGAGAGCTTT[A/G]TTAGTAGTCTCACAG | 22992 |
rs181607393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67159423 | TTCCTAAGCTACATT[A/G]TTTGTAAACTGGAAG | 22992 |
rs181615226 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67139544 | GCCACTGCACCCAGC[C/G]TCTTTTTGTTTTTTA | 22992 |
rs181631525 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67211813 | ATCCTAGAGTTACAT[A/T]ATCTGTTTGTTCCCT | 22992 |
rs181631734 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | KDM2A | GRCh38.p7 | 11:67129890 | CACTCCAGCCTGGGC[A/G]ACAGAGACTCTGTCT | 22992 |
rs181631762 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67173316 | TAGTAGAGACGGGGT[G/T]TCTCCGTGTTGATCA | 22992 |
rs181636279 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67193686 | ACCAACATGGCAAAA[C/T]GCCGTATCTACTAAA | 22992 |
rs181670272 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67178461 | TTAGTATATTCACAG[G/T]GTCATACAAATACCA | 22992 |
rs181683622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67125295 | GAGTGATCTTCCCAC[A/G]TCAGCTTCCCAGGTA | 22992 |
rs181696467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67215031 | AATAAAACAAATTAT[A/G]TAAGTATTGACATAG | 22992 |
rs181740725 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67121053 | TCCGACAGTTGTAAT[A/G]TGATTAATGTTGAAC | 22992 |
rs181758106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67144652 | AGCTCACTGCATCCA[C/T]AGTCTCCTGGGCTCA | 22992 |
rs181761542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67151830 | GCTTACTATAGCCTT[A/G]AACTCCTGGGCTTAA | 22992 |
rs181893826 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KDM2A | GRCh38.p7 | 11:67229432 | ATTTTTAGACTCTTA[C/T]ATGTCTGAAACTGGT | 22992 |
rs181905076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67251930 | TGGTTTTCAGGGCAA[A/G]GCACATCAGATTCCC | 22992 |
rs181968253 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67179999 | AAGTAGCACTTTGCA[C/T]ATGTAGGGAAATCTA | 22992 |
rs181969992 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67166726 | ATGGTGACCTCCCAG[C/T]AACTGGGGACCAAGA | 22992 |
rs181994658 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67235365 | GCTGGAGTGCAATGG[C/T]GCAGTCTTGGCTCAC | 22992 |
rs182067723 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185790 | ATAAAAGCATGAGTT[C/T]GGCCCCTTCGTGCTT | 22992 |
rs182069630 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67218767 | AGGTGTGCACCACCA[C/T]GCCCAGCTAATTTTT | 22992 |
rs182083531 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67132773 | GCATGAGCATTAACT[A/G]AGTGTCTGGGAACAT | 22992 |
rs182089219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67154658 | TGGCCAGGCTAGTCT[C/T]GAACTCTTGGCCTCA | 22992 |
rs182090113 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67140883 | GAGATTCTGGGTTAA[C/T]GTCATGAGGTATCAC | 22992 |
rs182098939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67122478 | ACTGTAGGCATGTGC[C/T]ACCACGTCCAGCTAA | 22992 |
rs182104239 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67174009 | CATGAGCCACCATGC[C/T]CACTTTGGGAGGCCA | 22992 |
rs182106102 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67204732 | TCCTGACCTCGTGAT[C/T]CACCCACCTCGACCT | 22992 |
rs182111895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67160259 | TGTAGCCTCGAGGGA[C/T]CATTATTGATGTCTC | 22992 |
rs182120362 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67220451 | AAATTCATGTATCTT[C/T]TTCTACACTGATGAC | 22992 |
rs182132366 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67242023 | AGGTTGCAGTGAGCC[A/G]AGATAGCGCCACTGC | 22992 |
rs182241482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206722 | AGCCTGAGCGACAGA[A/G]CGAGACTCCGTCTCT | 22992 |
rs182250061 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67243764 | AGGTTGCAGTGAGCC[A/G]AGATCGCACCATTGC | 22992 |
rs182322853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67169507 | GCCTCAGCCTCCTGA[A/G]TAGCTGGGATTACGG | 22992 |
rs182365510 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67167470 | TGTATCCCGACTCTT[C/T]TAGGATCATTCTGTA | 22992 |
rs182369987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67203874 | GGTGCGATCTTGGCT[C/T]ACTGCAACCTCTGCC | 22992 |
rs182379691 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67240578 | GGCTTTTGAGAATCC[G/T]TTCCCTCTCTGCCCA | 22992 |
rs182465787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67130590 | TCAAGGAATTGATAC[A/G]TTATGTATATCATGT | 22992 |
rs182501096 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67225018 | ATTTTTGTATTTCTA[C/G]TAGAGACGGGGTTTC | 22992 |
rs182504300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67189248 | GTTAAAAATCAATAA[C/T]AGGTAAAACTGGAAA | 22992 |
rs182505445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67162466 | CTGGAGTGCAGTGGC[A/G]TGACCTCAGCTCACT | 22992 |
rs182595898 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67256409 | TCAATATTTTTAAGT[C/G]TGTGAGGAGATGCTC | 22992 |
rs182632524 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67186327 | CAGAAACTTTGGAGG[C/T]CAGGAGGCAGTGAGC | 22992 |
rs182639793 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67163175 | CTAGCGCTACACTTT[C/G]GTATTTATGTTTGAC | 22992 |
rs182650356 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67126136 | CTGTAATCCCAGCTA[C/G]TCAGGAGGCTGAGGC | 22992 |
rs182654240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67147999 | GAGAGTCTTATAGCA[A/G]ATGTCTCTAGCTGAT | 22992 |
rs182660741 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67200800 | GCATGAGCTACCATG[A/C]CTTGCCTGAGATTAA | 22992 |
rs182664583 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67226264 | TCCATCTCAAAAAAA[A/T]AATAATAATATATCA | 22992 |
rs182671157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67216670 | TCACGCCTGTAATCC[C/T]AGCACTTTGGGAGGC | 22992 |
rs182671561 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67181513 | TGAAAATAATTTCCC[A/G]CTTTGTTTTAAAAGT | 22992 |
rs182700588 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KDM2A | GRCh38.p7 | 11:67152639 | TTAAAAATTGGCTAC[C/T]GGAAAAATTTAAATT | 22992 |
rs182721667 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67191276 | GTGATCTGCTCGCCT[C/T]GGCCTCCCAAAGTGC | 22992 |
rs182728854 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67157141 | ACACGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 22992 |
rs182736314 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67209233 | CCACCACACCGGGCC[G/T]AAAGGAACTATTTTT | 22992 |
rs182747686 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67226911 | GTGGGAGGATGATAG[C/T]CTGGGTGAAAGAGCA | 22992 |
rs182772018 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67152119 | CAGGAGTTGAAGAAC[C/T]GCCTGGTCAACATAG | 22992 |
rs182775703 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67167178 | CTTTGGAAAAACCAA[A/G]AATGTGCCTTAGATA | 22992 |
rs182800538 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | KDM2A | GRCh38.p7 | 11:67219559 | AAAATTTTAAATTTA[A/T]TTTTTTTTTTTTTAA | 22992 |
rs182803915 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185891 | GCGCCTTGATTTTAG[A/G]CTTCCCAGCCTCCAG | 22992 |
rs182805435 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67204121 | TACATTCTTGAAGGA[A/G]AGCATTTACTTGTTA | 22992 |
rs182881077 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67133652 | AGGTGATCTGCCCAC[C/G]TCGGCCTCCCAAAGT | 22992 |
rs182942408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67190479 | GGATTGTAAGAGAAT[A/G]CTATGCGTGGTGGCT | 22992 |
rs183025155 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67248825 | GGCAGAAAGCCCTGC[C/T]CTGCCCATCCCACAT | 22992 |
rs183059627 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67240921 | GTGTGAACAGCTGCC[A/G]CCCCCCACACACACA | 22992 |
rs183077317 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67214066 | ATTTTTTGAGACGGC[A/G]TTTCGCTCTTGTTTC | 22992 |
rs183138342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67177094 | GAAACCCTGTCTCTA[C/T]AAAAATACAAAAATT | 22992 |
rs183140310 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67142118 | ATCTCCGCTCACTGC[A/T]ACCTCCACTTCCCAG | 22992 |
rs183160284 | snp | C/T | 0.00113461 | 0.0237912 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255526 | TCCATCACACTCTCC[C/T]GGCTTGCGCAGGAGG | 22992 |
rs183181441 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67236176 | TGCTCTGTCACCCAG[C/G]CCGAAGTGCAGTGGC | 22992 |
rs183195196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67174579 | TAGGAGAGTGATACA[A/G]CTAATACTCCTGCAG | 22992 |
rs183214378 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67160777 | ACTCCATCTCAAAAA[A/C]AACAACAAAAAAAAA | 22992 |
rs183214857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67213905 | AGTCTTGCCCTGTTG[C/T]CCAAGCTGGAGTGCA | 22992 |
rs183226864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67195664 | GTTGTTCATGCTCTA[C/T]GCAGTCTGTATAACC | 22992 |
rs183230231 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67230801 | AAATTATAAAAGAAA[A/C]GACTGGTGAACATTT | 22992 |
rs183239055 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | KDM2A | GRCh38.p7 | 11:67208195 | ATAACTGCATTTTCC[A/G]AAATCATAATAAATT | 22992 |
rs183240485 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67170299 | TAAACAATAATATAG[A/C]TAGAAATGTAGTGTC | 22992 |
rs183245742 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67200427 | TTTCACCATGTTAGC[C/T]AGGATGATCGCGATC | 22992 |
rs183295573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67125928 | AGCATGGGTGACTGA[A/G]CAAGGCTTCACCTCA | 22992 |
rs183310230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67162886 | GCCCAGCTAATTTAA[C/T]AAATTTTTTAGAGAT | 22992 |
rs183316455 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67135291 | CAGGATGGTCTCGAT[A/C]TCTTGACCTCGTTCC | 22992 |
rs183333901 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67231248 | CCCAGATTCAAGCTT[C/T]AACTTGAAACTGACT | 22992 |
rs183337991 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67196532 | TTCCATTCACTGGAT[G/T]ATTATTTAGCCTTAA | 22992 |
rs183370631 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67134746 | CTGACCTCAGGTGAT[C/G]CACCTGCTTCAGCCT | 22992 |
rs183371221 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67123645 | GCAGTCCAGACTTTA[A/G]AGGAAGAGCCTTTCC | 22992 |
rs183397210 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67161180 | TAACTTGAGAACGCA[A/G]TGTGATCCTGTCTCT | 22992 |
rs183415085 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67170659 | ACCCAGTGATCCGCC[C/T]GCCTCAGCCTCTGAA | 22992 |
rs183456861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67236644 | TGCCAATCATACTTT[A/G]TGACTTTTGGGTAAG | 22992 |
rs183465179 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67217291 | ACAACTATGTCTCCA[A/T]ATCCAAAAGTCATTT | 22992 |
rs183469522 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67122851 | CAGCTAATTTTTTGT[A/G]CTTTTAGTAGAGACG | 22992 |
rs183481784 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67216457 | TTCATTCAGTTATAT[A/T]CCAGCTTGTGAAAAT | 22992 |
rs183564815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67145807 | CTGTTCTTTCTGAAT[C/T]ATACATTTTCCTTCC | 22992 |
rs183597553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67161317 | AGAAATTGTATCCAC[A/G]TGAAACCTTTGAATT | 22992 |
rs183616519 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67124243 | TCCTGACCTCAGATG[A/G]TCCACCCACATCAGC | 22992 |
rs183618399 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67143392 | AAATAGTGTTGGTTC[A/C]GTTTCTGAAAATTTC | 22992 |
rs183643163 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67177441 | TATTCTATAAGCTTT[C/T]GTCTACTAAAGTTTT | 22992 |
rs183651350 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67196802 | TGGTAATGGTTGCAC[A/C]ACATTGTGAATATAT | 22992 |
rs183766153 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | KDM2A | GRCh38.p7 | 11:67223597 | TATTTTTTTGTAGAA[A/G]CGAGGTTTTACTATG | 22992 |
rs183777012 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | KDM2A | GRCh38.p7 | 11:67221340 | TGCAGAGAAGAGTGT[A/G]GAACTATTAATGCTA | 22992 |
rs183793129 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67243597 | GGCAGGTGGATCACC[G/T]GAGGTCAGGAGTTCA | 22992 |
rs183843941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67186980 | ATAGGGGCACAGTAT[A/G]TAAGGATGTGGTTTT | 22992 |
rs183896845 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67184751 | CGACTGCATATGCAC[A/G]TGGACGGTCAGGCTC | 22992 |
rs183906360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67150296 | CACAGGTATTATTTG[C/T]TAGTCTGACAAGTAA | 22992 |
rs183909626 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67165981 | GTACCATGTATTATA[A/C]TGATGACTTAACAGT | 22992 |
rs183911252 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67218357 | TGACTATGCATTTAC[C/T]TGCTAGATACTACGC | 22992 |
rs183920077 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67249711 | CTTAGACTGTGGTAG[A/T]GCTAGAAGCCAATGG | 22992 |
rs183923408 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67202256 | TTAAGATGGAATCTA[C/G]TCCTGGTGGAGATGC | 22992 |
rs183935744 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67238910 | ATCACTAGAAACTCA[A/G]CCAGAGTGTGCACCC | 22992 |
rs183943355 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | KDM2A | GRCh38.p7 | 11:67208381 | CCTGGGCGTGAAATC[A/G]CTTAATTTTATATAG | 22992 |
rs183948401 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67247310 | GGCCAGGCCGGTCTC[G/T]AACTCCTAACCTCAA | 22992 |
rs183969307 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67128174 | CACCTGGCTTATTTT[A/T]AAATTCTTTCTAGAG | 22992 |
rs183971171 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67205465 | GGCAGGTGTTTGTTC[A/G]TCTTACAAGGAAGAC | 22992 |
rs183978085 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67242093 | ATAAAAATTAAAAAA[A/T]ATATATTTGTTTCAA | 22992 |
rs184020112 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67141300 | AAGTCAGAGTATTTG[C/G]GGCATCTTATCACCT | 22992 |
rs184032453 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67168452 | CCCTAGTGGCCAGCA[A/G]TCTTCTTGAGTGCTA | 22992 |
rs184039329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67187923 | AGAGGGGCCTGGTAT[A/G]GTGCCTCACACCTAA | 22992 |
rs184044700 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67167665 | CGCATAAGCTTCCTG[A/C]TAAATTCTGTAGACA | 22992 |
rs184046121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67154023 | CTTACCACAGATTTA[C/T]GGTTATACTGAAGAA | 22992 |
rs184063092 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67205844 | ACCATTTTCTGAATC[C/T]TTTAGCTTATATTTT | 22992 |
rs184068842 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67243303 | TAACAGAACTATCAA[A/T]CTGGGAGGCCTCCCT | 22992 |
rs184101846 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67226518 | ACGAGGTCAGGAGAT[A/C]GAGACCATCCTGGCT | 22992 |
rs184111023 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67131556 | AGCTGGGATTACAGG[C/T]GTGTGCCACCACGCC | 22992 |
rs184134886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67169234 | GCTGGGATTACAGGC[A/G]TGAGCCACTGCACCC | 22992 |
rs184144310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67132145 | GCTTTATACTACTAC[C/T]ATAAGGCCTATTCTG | 22992 |
rs184171755 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67127610 | CTGCGGCCACTGAAA[C/G]TCTGGCAATAGTCCC | 22992 |
rs184173344 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | KDM2A | GRCh38.p7 | 11:67148527 | GTAATCCGGCCGGGC[A/G]TGGTGGCTCATGCCT | 22992 |
rs184180525 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67190824 | ATGAAGTGTACAAAT[A/T]TCTAGAAACACAAAA | 22992 |
rs184237425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67125745 | GATTGCGCCACTGCA[C/T]TCCAGCCTGGGCGAC | 22992 |
rs184287976 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67214281 | GCAATCTCGGCTCAC[C/T]GCAAGCTCCGCCTCC | 22992 |
rs184291375 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KDM2A | GRCh38.p7 | 11:67154577 | AGCTGGGATTATAGG[C/T]ACCTGTCACACACCT | 22992 |
rs184502625 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206597 | AAAAAATTAGGTGGG[A/G]TAGTGGCGTGTGCCT | 22992 |
rs184507117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67232288 | TTAAGTTACCTTGAG[A/G]TAAAACTCAGGACAA | 22992 |
rs184637003 | snp | C/G/T | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67256638 | GGGAATGGAGCCCAG[C/G/T]CACCAGGGGTCTAAA | 22992 |
rs184647428 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KDM2A | GRCh38.p7 | 11:67188369 | CGCCTGTAGTCCCAG[C/T]GACTCGGGAGGCTGA | 22992 |
rs184660811 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67131201 | TGGTGGTGCACGCCT[C/G]TAGTCCCAGCTACTC | 22992 |
rs184663158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67192297 | TAACAAATGGCATCA[C/T]AGTGTACAAATCATT | 22992 |
rs184665209 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67227489 | ACTCTGTCCCAGAAC[C/T]GAAACTTTCATTGTT | 22992 |
rs184666249 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67153436 | TTTGGTTTAATGTGT[C/T]ATCAAACTTTGTATT | 22992 |
rs184693549 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67211922 | AGATACAGTGGAAAA[G/T]GATATCATTCTTGTT | 22992 |
rs184710783 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | KDM2A | GRCh38.p7 | 11:67229730 | CAGAAATTAGCCAGG[C/T]GTGGTGTTGCGCACC | 22992 |
rs184718586 | snp | A/G | 0.000182793 | 0.00955839 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67252746 | AGTAGGTGTAAGGCC[A/G]TTGTGCCCCAGGCCC | 22992 |
rs184756497 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | KDM2A | GRCh38.p7 | 11:67157573 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 22992 |
rs184779655 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67215164 | ATATAACAATTATTT[C/T]TAGGATGGTTGCCTA | 22992 |
rs184787646 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67257961 | GGTGATATTTGTGTA[A/G]TAAAATTTTTAAAAG | 22992 |
rs184813399 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | KDM2A | GRCh38.p7 | 11:67210229 | AGCCAGGCATGATGG[C/T]GTCCCCCATGTAGTC | 22992 |
rs184817476 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67197327 | CACAGGTGGGCACCA[C/G]CATGCCCAGATAATT | 22992 |
rs184829791 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67214527 | TATTTTTAGTAGAGA[C/T]GGGATTTCTCCATGT | 22992 |
rs184835666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67144900 | TTTGAGACAGAGTCT[C/T]GCTCTGTCATCCAGG | 22992 |
rs184835761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67177792 | CACAGTCATTTATTA[C/T]GTACTATTCCTAACA | 22992 |
rs184842339 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | KDM2A | GRCh38.p7 | 11:67233282 | CTAGCACTTTGAGAG[A/G]CCAAGGTGGGAGGAT | 22992 |
rs184863238 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67257260 | TTTTTTGGGGTTTGG[A/G]AAAACATGCATTTTT | 22992 |
rs184869527 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67171943 | GTCTTGATTACTATA[A/T]GTTTATAGTAAGTTT | 22992 |
rs184874278 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67178490 | CACTATCTAATTCCA[C/G]AACATTTTCATTGCT | 22992 |
rs184876047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67138075 | TGCTGGGATTACAGG[C/T]GTGAACCACCGCGCC | 22992 |
rs184908436 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67233382 | AAAAAGGCTCAGTGC[A/G]ATGTCTCATGCCTGT | 22992 |
rs184910539 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67125650 | TGGGGGTGGTGGTGC[A/G]TGCCTGTAATCCCAG | 22992 |
rs184914880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67145422 | TTGAACCCGGGAGGT[A/G]TAGGTGCCAGTGAGC | 22992 |
rs184963120 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67158054 | CATTACAGTATCATA[C/T]AGAATAGTTTCACTG | 22992 |
rs184967657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67198030 | AAAAGAACATTTGTT[C/T]ACTATTAAGATTGAA | 22992 |
rs184971915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67162048 | CAGTGAATTGTTCTG[A/G]ACTACTGTTCTGATT | 22992 |
rs184985419 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67139132 | AACCTTCAGTGAGTA[C/T]AGAAGGGGCCCATTA | 22992 |
rs185001471 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67172606 | GAACTGATTTTATTA[A/G]CTCTTATAGTTGTGT | 22992 |
rs185006978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67193353 | GTTTTTAATCTGCAT[A/G]TCCTGTAAGGATAAT | 22992 |
rs185008834 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67201642 | GTGTGGTGGCATGGG[C/T]CTGTAGTCCCAGCTA | 22992 |
rs185014770 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67164690 | TAGTGGCACAATCTC[A/G]GCTCACGGCAACCTC | 22992 |
rs185040117 | snp | A/C/T | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67120271 | TTTCCCTCCCGACTT[A/C/T]GGGCCAGGGCTTCCT | 22992 |
rs185107440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67183828 | AAAGAGGCAGGTGGG[A/G]CCAGGCACAGTGGGT | 22992 |
rs185224742 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | KDM2A | GRCh38.p7 | 11:67179507 | CTAATCTCGAACTCC[C/T]GACCTCAGGTGATCC | 22992 |
rs185242462 | snp | A/G/T | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67162326 | TTATTGCCTGTAAAT[A/G/T]TATAATGCTCACTTC | 22992 |
rs185246846 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67215959 | GGAAAGGTATGGTCA[G/T]AGTTGTGATAGGGGT | 22992 |
rs185257140 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67199080 | CCACTGCACCCAGCA[G/T]ATCAGTGATCTTTGA | 22992 |
rs185336393 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67237584 | TTACAGGCATGAGCC[A/T]CCTTACCCAACCAAC | 22992 |
rs185383040 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67122156 | AGGAAAGCGACAGAA[C/T]TGTATGTAGTATGTG | 22992 |
rs185442762 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67217487 | TCCCTCTTCTCTCCG[A/C]GTCCTGGATGGTGTA | 22992 |
rs185538786 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67161864 | AATGCTCTCAGGACT[A/G]AGGGAATGTATATTT | 22992 |
rs185542593 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | KDM2A | GRCh38.p7 | 11:67125373 | TTTTGTAGAGGTGGG[A/G]TTTTGCCGTGTTCCC | 22992 |
rs185560718 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67251824 | TGCAAACATGAGTTT[A/C]TTTCCCAAATCTGAA | 22992 |
rs185576399 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67204133 | GGAAAGCATTTACTT[A/G]TTATTTCTTAAATTA | 22992 |
rs185576602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185971 | TTCTGTCAACAGCAA[C/T]ACAAAATGGACTAAG | 22992 |
rs185582354 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67241147 | AGAGTCCTACTCTTC[A/C/G]TCAGTGCGAAGTGGG | 22992 |
rs185592869 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67219790 | CTCCTGGTTCAAGCA[A/G]TCCTCCCACCTCAGC | 22992 |
rs185626582 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67182369 | ATTTTATTATATTCA[A/T]AATTTGGGAAAAAGA | 22992 |
rs185647533 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67211529 | TGAGGTGGGAGAATC[A/G]CTTGAAACCAGGAGG | 22992 |
rs185665522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67144181 | AACTCCTGATGTCAC[A/G]TGATCTGCCTACCTC | 22992 |
rs185680262 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67148453 | AATAAGGGTTTTTTC[A/G]TGGGGTAAAACTCAA | 22992 |
rs185696202 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67228925 | AGATGAAGTCTTGCT[C/G]TGTTGCCCAGGCCGG | 22992 |
rs185715316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67170104 | TTATAACTACAAATA[C/T]AGGAAGTGAGAACAC | 22992 |
rs185719548 | snp | A/G | 0.0029071 | 0.0380144 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67207463 | TCTTACTATATTTAA[A/G]GATATTAGTGGCTCG | 22992 |
rs185726413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67189838 | AGTGAGACTCTGTGT[C/T]AAAAAACAAACAAAC | 22992 |
rs185729834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67246318 | ACCCTGAGGATAGAA[C/T]AGTACACAAAATAGA | 22992 |
rs185733435 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67225718 | AGGTTGCGGTGAGCC[A/G]AGATCACACCACTGG | 22992 |
rs185752119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67163627 | GGGAGGCCAAGGCAG[A/G]CAGATCATGAATGAG | 22992 |
rs185783880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67155989 | GCGCAGGGCTCACGC[C/T]TGTAATCCCAGCACT | 22992 |
rs185833980 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67126550 | CTGTCTCTACTAAAA[A/C]TACAAAAATTAGCCG | 22992 |
rs186075846 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67247225 | TTCCCTAGTAGTTGG[A/G]ATTACAAGCACGTGC | 22992 |
rs186107029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67134544 | GACAGTCAATCTGTT[A/G]CCGAGGCTGGAATGT | 22992 |
rs186123839 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | KDM2A | GRCh38.p7 | 11:67235451 | CTGGGATTACAGGCA[G/T]GCACCACCACCCTGG | 22992 |
rs186128043 | snp | G/T | 0.0236746 | 0.106192 | intron-variant | KDM2A | GRCh38.p7 | 11:67200217 | AATATTGTTTGTGTG[G/T]TTTTTTTTTTTCTTT | 22992 |
rs186133195 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67216283 | GAAGTATAATAAATA[A/G]TGGAAGGGAACACGA | 22992 |
rs186140302 | snp | A/T | 0.0759472 | 0.179459 | intron-variant | KDM2A | GRCh38.p7 | 11:67208243 | ATTATTATTAAAAAA[A/T]TTTTTTTTTTTTAAA | 22992 |
rs186148321 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | KDM2A | GRCh38.p7 | 11:67170447 | AGATGGAGTCTCGCT[C/G]TGTCGCCCAGGCTGG | 22992 |
rs186150105 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | KDM2A | GRCh38.p7 | 11:67234402 | CTTTCAGGAATAATT[A/T]GTAGAAGAGATGAGG | 22992 |
rs186191507 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67226321 | TCATTTGATGGATCT[C/G]ATTTTTCTGAAATAG | 22992 |
rs186241569 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67193722 | AAAAATTAGCCAGGC[A/G]TGGTGGCAGGCGCCT | 22992 |
rs186242362 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KDM2A | GRCh38.p7 | 11:67156506 | GCGGATCACGAGGTC[A/G]GGAGATCGAGACCAT | 22992 |
rs186248060 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KDM2A | GRCh38.p7 | 11:67166851 | GAAGGCCAAGGCGGG[C/T]GGATCACTTGAGGTC | 22992 |
rs186256183 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67173475 | ATTGGCCAGGCTGGT[C/G]TCCAGCTCCTGACCT | 22992 |
rs186256246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67130047 | TGCTCACTGCAACCT[C/T]CGCCTCCCGGGTTCA | 22992 |
rs186256558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67174168 | GAGGCTGAGGCAGGA[A/G]AATTGCTTGAACCTG | 22992 |
rs186261169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67151872 | ACCTCAACCTCCTGC[A/G]TAGCTAGGACTATAG | 22992 |
rs186264441 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67190535 | GAAGCCAAGGTGGGT[A/G]CATTGCCTGAGCTCA | 22992 |
rs186266710 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67194633 | TGGTGATTGCCTAGT[A/G]AAAAATAGAGGGCTC | 22992 |
rs186270568 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | KDM2A | GRCh38.p7 | 11:67160519 | GTTCACACCTGTAAT[C/T]CCAGCACTTTGGGAG | 22992 |
rs186276027 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67218697 | GCAACCTCCACCTCC[A/C]AGGTCCCAGTTCAAG | 22992 |
rs186280826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67194276 | ATCCTTTCCCAAACT[A/G]GGGGAGGGTGGTTGC | 22992 |
rs186284245 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67213150 | CCCACAGTTAACATC[A/T]GGGTATCCTCTAGAC | 22992 |
rs186294728 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67239800 | AAGCCTTCCCTTTGG[C/T]TGGCGCCTTCAGAAG | 22992 |
rs186299399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67159924 | ATGATGAAAAAATTC[A/G]GGAGATGGATAGTGG | 22992 |
rs186351417 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67122507 | AATTTTTGTATTTTT[A/G]GTAGAGAACAGGGTT | 22992 |
rs186351579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67140884 | AGATTCTGGGTTAAC[A/G]TCATGAGGTATCACC | 22992 |
rs186361187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67154893 | CGTTGTATGGATATA[C/T]CACATTTTGCTTATT | 22992 |
rs186364124 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67212121 | GCAATGTGGCAAGAC[C/T]CAGTCTTTTAAAATT | 22992 |
rs186367612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67169904 | CTGGGATTACAGGCA[C/T]GTGCCACCATGGCAG | 22992 |
rs186368108 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KDM2A | GRCh38.p7 | 11:67253712 | CTCAGATATGACGCT[A/G]TGGAAGAATAGAAGA | 22992 |
rs186369027 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67132851 | AACTCTGGAGTTGGG[A/G]CCTAGCAATCTGTGT | 22992 |
rs186416336 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67140581 | ACATGGTGAAACCCT[A/G]CCTCTACTAAAAATA | 22992 |
rs186462017 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67173696 | ACTTAGCCTGGTTTT[A/T]ATTTTTATTATTTTT | 22992 |
rs186583162 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67131412 | TTAGTGTTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 22992 |
rs186585181 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67140118 | ATAATCCCAACACTT[C/T]GGGAGGCTAAGGCAG | 22992 |
rs186658573 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67133248 | GGGATTACAGGCGTG[C/T]GCCACCACACTGCGC | 22992 |
rs186745303 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67196904 | ATTTTTTACAAGTTG[A/G]AAAAAAAATAGACTC | 22992 |
rs186761070 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | KDM2A | GRCh38.p7 | 11:67214326 | TCTCCTGCCTCAGCC[C/T]CCCGAGTAGCTGGGA | 22992 |
rs186762528 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67177452 | CTTTTGTCTACTAAA[C/G]TTTTTTTTTTAACTT | 22992 |
rs186768578 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67242056 | TCCAGCCTGAGCAAC[A/T]GAGTGAGACTCCATC | 22992 |
rs186781701 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67232675 | TCTTAAGGAATCCAG[A/T]CTTGAGCTTTTTTTT | 22992 |
rs186814142 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67159710 | TTGTCAGGCATTTGA[G/T]AGGTACTGGGAAGAC | 22992 |
rs186824385 | snp | C/T | 1.6582e-05 | 0.00287936 | missense, nc-transcript-variant, utr-variant-5-prime | KDM2A | GRCh38.p7 | 11:67121339 | CCGAAGAAGAAAGGA[C/T]TCGTTACAGCCAGAG | 22992 |
rs186880186 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67240582 | TTTGAGAATCCTTTC[A/C]CTCTCTGCCCAGGCA | 22992 |
rs186893174 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67200978 | GCGGGTGGATCACGA[C/G]GTCAGGAGATTGAGA | 22992 |
rs186903883 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67216874 | GCGGTGAGCTGAGAT[C/T]GCGCCATTGCACTCT | 22992 |
rs186910431 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67182217 | AGTTTCATTAATATC[C/T]GTGATTCCCTTCCTT | 22992 |
rs186918178 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67236205 | GCGTGATCTAGGCTC[A/T]CTGCAGCCTCCGCCT | 22992 |
rs186954908 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67203958 | GCCGCGTACCACCAC[A/G]CCCAGCTAATTTTTG | 22992 |
rs186962491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67148006 | TTATAGCAAATGTCT[C/T]TAGCTGATCATCTAG | 22992 |
rs186970196 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67163180 | GCTACACTTTCGTAT[A/T]TATGTTTGACCTTCC | 22992 |
rs186972163 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | KDM2A | GRCh38.p7 | 11:67126241 | ACAAGAGCAAAACTC[C/T]GTCTCAAAAAAAAAA | 22992 |
rs187040991 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67171767 | AAGTGATCCTCGTGC[C/G]TTGGCCTCCCAGAGT | 22992 |
rs187046396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67167194 | AATGTGCCTTAGATA[C/T]AACATCTAAACTCAG | 22992 |
rs187053615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67142132 | CAACCTCCACTTCCC[A/G]GGTTCAAATGATTCT | 22992 |
rs187094179 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | KDM2A | GRCh38.p7 | 11:67152157 | CTGTGTCTATTAAAA[A/T]TACCAAAAAGCCAGG | 22992 |
rs187096987 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | KDM2A | GRCh38.p7 | 11:67123950 | CCAAAGTGCTGAGAT[A/T]ACAGGCATGAGCCAC | 22992 |
rs187106935 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67125808 | AATTAGCCGGGCGTG[G/T]TGTAGGGCGCCTGTA | 22992 |
rs187124641 | snp | C/T | 0.0799831 | 0.183287 | intron-variant | KDM2A | GRCh38.p7 | 11:67162648 | TGACCTCAAGTGATC[C/T]GCCCGCCTCGGCCTC | 22992 |
rs187134078 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67225309 | CTGAAAATGTCAAAT[C/T]CTAGAAAACATAGCA | 22992 |
rs187139317 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67189267 | TAAAACTGGAAAGGT[C/T]ACAAAATTGTGGAAT | 22992 |
rs187162763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185799 | TGAGTTCGGCCCCTT[C/T]GTGCTTTCTCTCATT | 22992 |
rs187164420 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67218999 | CCCTGAATTGTAAAC[A/T]ATCTTGTACAGAGCC | 22992 |
rs187189386 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67125985 | GCACAGTGTCTCACG[C/T]CTGTAATCCCAGCAC | 22992 |
rs187194378 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67147249 | TCAGGTTAAAAGATA[G/T]GACTTCCACTGGGCC | 22992 |
rs187217702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67253891 | CTTTATGGTGGAGGT[A/G]GAGTCAAAAGCTATT | 22992 |
rs187237566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67244742 | TGTAATCCCAGCACT[A/G]TGGGATGCCAAGGCG | 22992 |
rs187296775 | snp | C/T | 0.000665967 | 0.0182357 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67180147 | TGAAGGAAAAAGAAC[C/T]TTTGACTTGGAAGAG | 22992 |
rs187303145 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185211 | CAATAATTAAAATGA[A/C]AACTTAGATTCAAAG | 22992 |
rs187310954 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67151303 | CATGTGAAATGTGGC[A/T]ACTATGAATTAAGAT | 22992 |
rs187325411 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67209385 | TAAGAATTCCAGTAA[C/T]ATTATTTATTTATAA | 22992 |
rs187328713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67145704 | CCCTTTCTCTTTTCT[C/T]ATTACTTGAAAATGA | 22992 |
rs187336182 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206868 | AACAAGAATCTGATA[C/T]AGATTTTCGTGTCCA | 22992 |
rs187339402 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KDM2A | GRCh38.p7 | 11:67191462 | ACAAAATACTTGCAT[A/G]CTAAATTCAGCAGCA | 22992 |
rs187344207 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67226981 | AAAAGGCAACAAAAT[A/G]TATTTAGGATAGTCC | 22992 |
rs187352662 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67249089 | GAAAGGAATTTTCTT[A/T]CTTTTTATTTCTTCC | 22992 |
rs187414056 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67203539 | TAATAAATAAGTAGT[C/T]TAGTAATAAAAGAAT | 22992 |
rs187434396 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67230760 | GGGATGACTTATTTA[C/T]CGCTTTGCGCCTTCT | 22992 |
rs187460622 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67129360 | TTGGGAGACCAAGGC[C/T]AGTGGAATGCTTGAC | 22992 |
rs187463022 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67214036 | CCTGGCTGTTTTTTT[A/T]ATTTTATTTTATTTA | 22992 |
rs187468336 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67187735 | CCCGCCACCACGCCC[A/G]GCTAAATTTTGTATT | 22992 |
rs187477137 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67153798 | CCAGCCTTGAGTAAC[A/T]GTGAGACCCTGTCTC | 22992 |
rs187477277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67195911 | GCTCCAATAAGGAAT[A/G]ATTTTTCTACCACTT | 22992 |
rs187478278 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67230969 | TTTTTTTGTTTGTTT[G/T]TTTTTGAGACAGGGT | 22992 |
rs187487979 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255688 | GCTTGTTCACATAAT[G/T]AGGTTTCCCACCCCA | 22992 |
rs187501247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67166474 | TACAGGAGTGAGCCA[C/T]GGTGCCTGGCTGAGA | 22992 |
rs187521271 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67131474 | TGGAGTGTAGTGGTG[C/T]GATATTGGCTCACTG | 22992 |
rs187563174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67220671 | TACCTTAAGGCAAGA[A/G]TTGACAAACTTTTCC | 22992 |
rs187591467 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67257160 | AGCAGGGATTGTGCC[A/G]GGAGAGTGCCTCTGA | 22992 |
rs187602061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67191236 | TTCACCATGTTGGCC[A/G]GGATGGTCTCGATCT | 22992 |
rs187604540 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67156918 | GAAATAGGAGCTTCA[C/G]TGCCCACAAATAAAC | 22992 |
rs187621177 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67170784 | CACCTTCTCTCTCTC[C/T]GCCAGACCCATTTAA | 22992 |
rs187639166 | snp | A/G | | | missense, intron-variant | KDM2A | GRCh38.p7 | 11:67250741 | TGTCTGTCTTCCGCT[A/G]CCTCAGCCGCAGAGA | 22992 |
rs187702136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67134767 | GCTTCAGCCTCTCAA[A/G]GTGCTGGGATTACAA | 22992 |
rs187711250 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | KDM2A | GRCh38.p7 | 11:67236754 | ATACTTAATAAGCAG[G/T]GCATTATTACAGCCA | 22992 |
rs187794782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67232075 | GTTCAGTCAGAGAGA[A/G]GTTAATATGCATGTG | 22992 |
rs187839124 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67161203 | CTGTCTCTATTAAAA[A/T]TTTTTTTAAATTGAA | 22992 |
rs187878644 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67196656 | TGTAATTCCACTGAC[A/G]TGAAGTATATAGAGT | 22992 |
rs187930090 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67161510 | ATTTTATATTACTAC[C/G]TATTACTATTATATG | 22992 |
rs187930586 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67130514 | TTAGACAGCCTTAAA[A/G]CTGTGAAGTTGCAAG | 22992 |
rs188003686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67228460 | ACTTTGGGAGGCCAA[A/G]GTGGGCGAATGGCTT | 22992 |
rs188019381 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67181005 | GACAGGGTGATGATA[A/T]TTTCTGTTTAGCATT | 22992 |
rs188023727 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67216614 | AATGAGAATAGATAA[C/T]GCCTTGTTTAAAACA | 22992 |
rs188028725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67157295 | TCCATCCAGCCTGGG[C/T]GACAGAGCAAGACTC | 22992 |
rs188064169 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67256453 | TATGGCAAGAGCTTA[C/T]AAATGATTGATGCAA | 22992 |
rs188124002 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | KDM2A | GRCh38.p7 | 11:67177247 | CTCCAGCCTGGGCAA[C/G]AGAGCAAGACTCCGT | 22992 |
rs188161511 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67214110 | CAGTGGCACCATCTC[A/G]GCTCACCAGAACCTC | 22992 |
rs188215946 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67239324 | AACTGCTGCAGGATT[A/G]CTGCGCAGACATTTC | 22992 |
rs188220496 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67202259 | AGATGGAATCTACTC[C/G]TGGTGGAGATGCTGT | 22992 |
rs188228317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67218410 | TGTCTCATTTTGTTA[C/T]AAGGAATATAAATGA | 22992 |
rs188266227 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67163051 | ATTGAACTGTATCCT[A/G]CTTTTGTTAGTTACT | 22992 |
rs188270624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67135301 | TCGATCTCTTGACCT[C/T]GTTCCACCTGCCTCG | 22992 |
rs188285108 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67184872 | CAATAATAAAACACA[A/G]AAAACCCTGGGGAAG | 22992 |
rs188298747 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67166056 | GTTTCCCTTTTCTGT[A/G]TTTGTTGATACAGAA | 22992 |
rs188311188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67200461 | TCACCTCATGATCCG[C/T]CCGCCTCAGCCTCCC | 22992 |
rs188354442 | snp | A/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67205925 | TTATTCTTCTCCCTC[A/T]TTTCCTAAAGCCTTT | 22992 |
rs188364884 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67162178 | TTTGGTAAATCTTCT[C/G]TTTCTCTTGGCTGTA | 22992 |
rs188365085 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67243307 | AGAACTATCAAACTG[A/G]GAGGCCTCCCTCCAG | 22992 |
rs188370930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67222896 | GAGAAGAAAAATAAG[A/G]GGGAAAAAAAAAAAA | 22992 |
rs188426121 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67168892 | TTATTCAAGTACATA[C/T]TAAGGCTATGAAGTG | 22992 |
rs188430310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67125463 | CATTTTTTGGGGGGA[A/G]AAAAAAATCAGAAAT | 22992 |
rs188434252 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67188299 | CATCCTGGCTAACAC[A/G]GTGAAACCCCGTCTC | 22992 |
rs188434417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67145338 | AAACACACACACACA[A/G]AATTAGCCAGGTGTA | 22992 |
rs188512000 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67205521 | CAGCCTCGACCTCCT[C/G]GGCTCAGGTGATTCT | 22992 |
rs188518192 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67242135 | ACCAGTGTGATTCAC[G/T]TAAGTGGCATTTTCT | 22992 |
rs188559603 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67175391 | CAGTGAGCTGTGATC[A/G]TGCCACTGCACCCCA | 22992 |
rs188567622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67141583 | AAGGCAGGAGAATGG[C/T]GTGAACCCGGGAGGC | 22992 |
rs188573487 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67127764 | CGAGGCTGGAGTGCT[A/G]TGACGCAATCTGGGC | 22992 |
rs188579536 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67149078 | AGATGAAAAAGCAGA[A/T]TTTTTTCCCCTGAAG | 22992 |
rs188648894 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67126752 | CCAAGCTTCATTATT[G/T]ACCTATTACGTGTGG | 22992 |
rs188659829 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67201279 | TGACATAGTGATTCT[C/G]CTGGTAAATCTGGAC | 22992 |
rs188665739 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67164158 | CTTGACATTTTCACA[G/T]GAGAAAATGGAAGCT | 22992 |
rs188673676 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67226583 | AAAAATTAGCCGGGC[A/G]TGGTGGCGGGCGCTT | 22992 |
rs188784136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67221719 | TCATACCTGTAATTC[C/T]AACCCTTTGAGAGCC | 22992 |
rs188786159 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67152753 | GCTGTAGAATTTCAT[A/G]TGGATCATTCCATAG | 22992 |
rs188800826 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant, utr-variant-5-prime | KDM2A | GRCh38.p7 | 11:67186396 | CTGTCAACCAAGCAT[A/C]CTATATCTGGCAAAA | 22992 |
rs188819338 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67123512 | ATTTCTTGAATTTAA[C/G]TTTTCTTTGGGAACA | 22992 |
rs188852042 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67160859 | GTGCCTGTAGACCCA[C/G]CTACTTGGGAAGCTG | 22992 |
rs188866054 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67217432 | ACTCTGGAAGCCAGA[C/G]AGAGTGTTTAAGGGA | 22992 |
rs188909393 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67164717 | CCTCCACCTCCCAGG[G/T]TCAAGCGATTCTTCT | 22992 |
rs188916295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67148460 | GTTTTTTCATGGGGT[A/G]AAACTCAAATAATAG | 22992 |
rs188939718 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67208685 | CTGAGGCATGAGAAT[C/T]GCTTGAACCTGGGAG | 22992 |
rs188949882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67248508 | TTTGGTTTGGTATGT[C/T]TTTCCTTTGGTTAAT | 22992 |
rs188952354 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67182462 | CTGCAGACAGTGGTG[C/T]TCATTGTGGTCCTGA | 22992 |
rs188978015 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KDM2A | GRCh38.p7 | 11:67229943 | GCACTTTGGGAGGCC[A/G]AGGAGGGCCAATCAC | 22992 |
rs188997319 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67252933 | TGCATTATTGGCAGT[G/T]CTTCTTAGCATCACT | 22992 |
rs189049370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67193764 | TACTTGGGAGGCTGA[A/G]GCAGAAGAACTGCTT | 22992 |
rs189061464 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67211925 | TACAGTGGAAAATGA[C/T]ATCATTCTTGTTAGA | 22992 |
rs189074417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67130605 | ATTATGTATATCATG[C/T]AGATAGACATACATT | 22992 |
rs189094372 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67204906 | GTTTATTCATATCAT[A/G]GTAAACATTTGTGTT | 22992 |
rs189124132 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67233312 | TCACCTGAGGTCAGG[A/T]GTTCGAGACCAGCCT | 22992 |
rs189133845 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67215009 | AACACCTTTTATTGG[A/G]TTAAAAAATAAAACA | 22992 |
rs189136151 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67257398 | TTTTAGAGGTGAGGG[C/T]TGGTCCATGTGGAGG | 22992 |
rs189141146 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67154645 | GGTTTTGCCATGTTG[G/T]CCAGGCTAGTCTCGA | 22992 |
rs189142147 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206973 | TAATTATCTTCATGG[A/G]CTAGGATATTAGCAA | 22992 |
rs189142224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67189530 | GGATTTTGAGGCCAG[C/T]TTGGGCAACATAGCA | 22992 |
rs189164632 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67188406 | AGAATGGCGTGAACC[C/T]GGGAGGTAGAGCTTG | 22992 |
rs189166602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67224182 | TCAGGAACACTACCC[A/G]ATATAGAGTTTGTAA | 22992 |
rs189199990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67154983 | TGCTATCAGCATTTG[C/T]GTGTAAATATTTGAA | 22992 |
rs189204097 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67170007 | GTGATTTGCCCACCT[C/T]GGCCTCCCAGAGCGC | 22992 |
rs189217759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67132999 | TAAACTTTGTAACTG[A/G]TGGATAGCAGCATGT | 22992 |
rs189279955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67172082 | GCAGCCTCAACCTCC[A/G]GGACTCAAGCCATCC | 22992 |
rs189282758 | snp | A/C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67172697 | TGTAATTTGTGAATA[A/C/G]ATGTAGTTTTACTTG | 22992 |
rs189286501 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67138284 | AACAAAAATGTGTTA[G/T]GTAGTCCTAAAAATA | 22992 |
rs189288716 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67211704 | ATTCAAAAACTTAAT[A/C]TTCATTTCTAAAAAC | 22992 |
rs189291101 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67193610 | TCACGCCTGTAATCC[C/T]GGCACTTTGGGAGGC | 22992 |
rs189305873 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67229122 | TTCTAGGCACTATAC[A/T]AAGCAATTTACATTT | 22992 |
rs189320613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67210505 | TGAATTTATTCACTC[C/T]GTCCCTAGTTTTAAT | 22992 |
rs189344558 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67158393 | GCTCTGAATATTTAT[A/G]TGTAGGTTTTTGTGT | 22992 |
rs189362118 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67120883 | AGTGGTGCTTCACCT[A/G]GTCAGCTCTCTGGAG | 22992 |
rs189364815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67243675 | AAAAATTAAGCCAGG[C/T]GTGGTGGCATGCGCC | 22992 |
rs189366553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67139468 | CAGGCTGGTCTTGAA[C/T]TCCTGACCTCTGGTG | 22992 |
rs189381894 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | KDM2A | GRCh38.p7 | 11:67198489 | GCACTTTGGGAGGCC[G/T]AGGCGGGCGGATCTC | 22992 |
rs189415305 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | KDM2A | GRCh38.p7 | 11:67169309 | TAAATTTTTTTTTTT[A/T]AAATCGTATCACAGT | 22992 |
rs189421984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67233608 | AGTGAGCCGAGATTG[C/T]GCCATTGCACTCCAG | 22992 |
rs189422727 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KDM2A | GRCh38.p7 | 11:67132311 | TTTTTGGATATGGAG[C/T]CTCACTGCGATGTCC | 22992 |
rs189430370 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67131595 | TTTTGTATTTTTAGT[A/G]GAGATGGGGTTTTAC | 22992 |
rs189433221 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206686 | AGGTTGCAGTGAGCC[G/T]AGAGCGTGCCACTGC | 22992 |
rs189506982 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | KDM2A | GRCh38.p7 | 11:67124300 | TGAGCCACCGTGCCC[C/G]GCTTCACTTTATTTT | 22992 |
rs189510008 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67143572 | CTACTTTTTCTTACT[C/G]AGTGGAATTATATTT | 22992 |
rs189559762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67157723 | GCACTCCAGCCTGGG[C/T]GACAAAAGCAAGACT | 22992 |
rs189568751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67128222 | TGTCCAGGCTGGTCT[C/T]GAACTCCTGGGCTTA | 22992 |
rs189597899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67192856 | GGCCAAAGAGTATAC[A/G]TTTTCACCTTGTCAA | 22992 |
rs189616463 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67216020 | TTCAGTTCATGTATA[C/T]TTAATATACCCTGGA | 22992 |
rs189631616 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67199677 | TTGGTTTATGAAGTT[G/T]AAGAAACCATCTTTG | 22992 |
rs189633794 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67234411 | ATAATTAGTAGAAGA[G/T]ATGAGGGGAAAAGTG | 22992 |
rs189658456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67178716 | TGTCATGGCACATAG[C/T]GTTATTTCATTCCTT | 22992 |
rs189683982 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | KDM2A | GRCh38.p7 | 11:67215246 | ATAGTTTTTTGTTAT[A/G]TATTTTAAGAAATTC | 22992 |
rs189692995 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67257969 | TTGTGTAATAAAATT[C/T]TTAAAAGACAAAAAA | 22992 |
rs189693347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67134670 | TCGCCACGCCCAGCT[A/G]ATTTTTATATTTTTA | 22992 |
rs189693691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67179710 | TCCCTGTGAAAAAAT[C/T]ATATTTTGTATCCTG | 22992 |
rs189702700 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67145530 | GCCATCCCTTTGAGG[A/G]GGAATATGGTAGCAC | 22992 |
rs189706593 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67162388 | ACAGGAAAGTAGATA[C/T]GATTTTTATTTTATT | 22992 |
rs189735986 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67154024 | TTACCACAGATTTAC[A/G]GTTATACTGAAGAAA | 22992 |
rs189795043 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67241540 | GAGCACACAGGATTA[A/T]GAGAAAAATTATTAG | 22992 |
rs189848554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67241519 | AAAGTCCTGGTCTCC[A/G]GGACAGAGCACACAG | 22992 |
rs189848784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67140878 | TACCAGAGATTCTGG[A/G]TTAACGTCATGAGGT | 22992 |
rs189853088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67122295 | ACATTTTCTAGTGAT[C/T]CTTACTCTTTTTGAG | 22992 |
rs189858410 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67220234 | CCAGGCTTGTCTTGA[A/G]CTCCTGGGCTCAAGT | 22992 |
rs189935944 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67167265 | ATCTTGAATTGATAG[C/T]CACATTTTGTTGTTG | 22992 |
rs189940101 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67204683 | TTTTTAGTAGAGATG[C/G]GGTTTCACCGTGATA | 22992 |
rs189941112 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67184387 | GTAATCCCAGCACTT[C/T]GGGAGGCCGAGGCGG | 22992 |
rs189944306 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KDM2A | GRCh38.p7 | 11:67159727 | GGTACTGGGAAGACA[A/G]TGGTGAAAAAGAGAT | 22992 |
rs189945224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67186197 | CCTCACCAAGACACA[C/T]TATAATCAAACTTTC | 22992 |
rs189961679 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67122019 | AGCCATGCTTTCCTC[C/G]TAAGGTTTCCCTATT | 22992 |
rs189966107 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67217536 | GCCTTAATGCTGTTG[C/G]ATCAAGTGAAGGATA | 22992 |
rs190069959 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | KDM2A | GRCh38.p7 | 11:67244910 | AGAATGGCGGGAACC[C/T]GGGAGGCGGAGCTTG | 22992 |
rs190072538 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67189899 | TAAAATCAACAACCT[A/G]ACCTTACAACTTAAA | 22992 |
rs190080949 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KDM2A | GRCh38.p7 | 11:67163120 | GTCAGACTGATATCC[A/G]GAATTTTGCTCTTGC | 22992 |
rs190086954 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67207833 | AGTTTGAGAGCAGCC[A/G]GGGCAACATGGTGAA | 22992 |
rs190087149 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67126016 | TTCGGGAGGCTGAGG[C/T]GGGTGGATCACCTGA | 22992 |
rs190089251 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67147764 | CTCACTGCAACTGCC[A/G]CCTCCTGGGTTCAAG | 22992 |
rs190090162 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67144403 | GATTACAGGCATGCA[C/T]CACCATGCCTGGCTA | 22992 |
rs190131688 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67177890 | GTAATGTGTTGTGCT[A/G]TGATGTCCTGATGGC | 22992 |
rs190197740 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67140264 | CCAGGTAATTGGGAG[G/T]CTGAGGTGGAAGGAT | 22992 |
rs190203923 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KDM2A | GRCh38.p7 | 11:67201912 | ATGAGCTCTGATCTT[A/G]CCACTCTATTCCAGC | 22992 |
rs190234119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67203843 | CTTGCTGTGTCGCCC[A/G]GGTCCGGAGTGCAGT | 22992 |
rs190236665 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67238152 | TGGTCTTAGTAATTC[G/T]TATCTTTTTTGCCTA | 22992 |
rs190323139 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67225490 | AAAATACAACAATTG[A/G]CCAGTCACGCTGGCT | 22992 |
rs190360661 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | KDM2A | GRCh38.p7 | 11:67125208 | TTTTTATTTGAGATA[A/G]GGGTCTTTGTCGCCC | 22992 |
rs190361837 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67256013 | CCAACCTGCCTCCCA[C/G]CCAGGCTCCTCCAGG | 22992 |
rs190367838 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67197543 | TCTTGGATAGCTAAT[A/C]ATTGGCAAAATGCAG | 22992 |
rs190378777 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67161969 | ACTCAGTTTTCAGTA[C/T]TTATATTATGCTCTT | 22992 |
rs190402390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67226172 | TGAGGCAGGAGAATT[A/G]CTTGAACCCAGGAGG | 22992 |
rs190410660 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67181177 | TGCTTCTTACTAAGC[A/T]TATATTTTATTGACT | 22992 |
rs190414981 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67246683 | TCCGAATTGTGCAGC[C/G]TTTGTGGAGAACCAC | 22992 |
rs190438906 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67231084 | ACCTCACCCTCCCTA[A/G]TATCTGGGACCACAG | 22992 |
rs190462307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67251845 | CAAATCTGAATTAAT[A/G]TATAGTGTATCTAAA | 22992 |
rs190480553 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | KDM2A | GRCh38.p7 | 11:67218763 | TTACAGGTGTGCACC[A/G]CCATGCCCAGCTAAT | 22992 |
rs190538945 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67203969 | CCACGCCCAGCTAAT[A/T]TTTGTATTTTTAGTA | 22992 |
rs190548280 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67239856 | CTGGCCCTAGGTTCT[A/C]CTATTGCAGTGGTGG | 22992 |
rs190556633 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185800 | GAGTTCGGCCCCTTC[A/G]TGCTTTCTCTCATTC | 22992 |
rs190588761 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67235596 | GCGTGACACCGCGCC[C/T]GGCTGCTTTTTTGTT | 22992 |
rs190616293 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67152036 | AAATTAATTTCCCGC[C/T]GGGTGCAGTGGCTCA | 22992 |
rs190622825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67167134 | TGTTAGCACCCAAGG[A/G]GACAAATATATGCAT | 22992 |
rs190627546 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67130269 | TCACGGCACCTGACT[C/T]CCTCACAGGTGCACC | 22992 |
rs190688183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67190770 | TTTAAAAAAAAAAAT[A/G]CTACGAACAATTGTT | 22992 |
rs190699506 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67156532 | ACCATCCTGGCTAAC[A/G]CAGTGAAACCCCGTC | 22992 |
rs190703361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67141007 | CTTACCTCATGCTTG[C/T]TCAAGTCAAAGGTTG | 22992 |
rs190705459 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67122818 | GTAGCTGGGACTATC[C/G]GCGCCCACCACTACG | 22992 |
rs190707852 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | KDM2A | GRCh38.p7 | 11:67226504 | AAGGCGGGCAGATCA[A/C]GAGGTCAGGAGATCG | 22992 |
rs190725975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67174535 | CTTGCATCTAGTGTT[A/G]CTTCCTCATATTTCT | 22992 |
rs190733919 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67195317 | AAGGCTGCAGTGAGC[C/T]GAGATCGCACCACTG | 22992 |
rs190735253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67125694 | TGAGGCAGGAGAATC[A/G]CTTGAACCTGGGAGG | 22992 |
rs190743236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67160580 | AGTTTGAGACCAGCC[C/T]GGCCAACATGGTGAA | 22992 |
rs190832517 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67152256 | AGGCGGAGGTTGCAG[A/T]GAGCCGAGATTGCAC | 22992 |
rs190850710 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67173767 | GCCCAGACTGGAGTG[C/T]AGTAGCCCCATCATA | 22992 |
rs190862863 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KDM2A | GRCh38.p7 | 11:67212909 | CCATGGACAACACAC[A/G]GGGATGGGAGATGGT | 22992 |
rs190866908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67253781 | ATAGGGTAACTATAA[A/G]CAGATAACTACCTAC | 22992 |
rs190954755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67170657 | TCACCCAGTGATCCG[C/T]CCGCCTCAGCCTCTG | 22992 |
rs190967664 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | KDM2A | GRCh38.p7 | 11:67208244 | TTATTATTAAAAAAA[A/T]TTTTTTTTTTTAAAG | 22992 |
rs190971263 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67247292 | ATGGGGTGTCACCGT[C/G/T]TTGGCCAGGCCGGTC | 22992 |
rs190999400 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67133650 | TCAGGTGATCTGCCC[A/T]CCTCGGCCTCCCAAA | 22992 |
rs191023543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67170292 | TATTAGATAAACAAT[A/G]ATATAGCTAGAAATG | 22992 |
rs191038243 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KDM2A | GRCh38.p7 | 11:67213627 | AGTTAGGTGCGGTGG[C/T]GGGTGCCTGTAATCC | 22992 |
rs191056977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67230792 | GCATTTTCTAAATTA[C/T]AAAAGAAAAGACTGG | 22992 |
rs191069592 | snp | A/C/G | 8.35686e-05 | 0.0064636 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67254925 | TACGGCGCATTGCCA[A/C/G]CGTCACCTTGATCGA | 22992 |
rs191086872 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67194383 | AACTCAGATAAAAGT[C/G]TTTCTGAGGCGTAGG | 22992 |
rs191097382 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67160250 | GTTTGTCTTTGTAGC[C/G]TCGAGGGATCATTAT | 22992 |
rs191101428 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67130589 | GTCAAGGAATTGATA[C/T]ATTATGTATATCATG | 22992 |
rs191126607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67230182 | CTCCGTCTCAAAAAA[A/G]AAAAAAAATACATCT | 22992 |
rs191238037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67156026 | GGCTGAGGGCAGACG[A/G]ATCACCTGAAGTCAG | 22992 |
rs191283152 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67236287 | AGGTGTGTGCCACCA[C/T]GCCTGGCTAATTTTT | 22992 |
rs191287037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67217050 | AGATCGAGAACATCT[C/T]GGCCAACATGGTGAA | 22992 |
rs191307964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206295 | AATTAGGCAGGCGTG[A/G]TGGCACACGGCCATA | 22992 |
rs191326650 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67223321 | ATAATTAATACAGTC[C/T]TATAAGTTACGAGTA | 22992 |
rs191331286 | snp | G/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, utr-variant-3-prime | KDM2A, LOC107984341 | GRCh38.p7 | 11:67117658 | GGGAAACCAAGGCAG[G/T]GAGAAAAAGATTTGT | 22992 |
rs191335734 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67213058 | TTCTTTGAAATGGAA[C/T]AGCAGGTTAACCTTA | 22992 |
rs191337620 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67163465 | CATTTAATGCCATTG[C/G]AGAAGAGGCAAGTAT | 22992 |
rs191357763 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | KDM2A | GRCh38.p7 | 11:67200568 | CCAAGTTGGAGTGCA[A/G]TGGTACAATCATGGC | 22992 |
rs191358180 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67201203 | TGTCTCAAAAAAAAA[A/T]ATATATATATATATA | 22992 |
rs191358222 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67157797 | CATTTGTTACAACTG[A/C]TGAACCAATAATGAT | 22992 |
rs191365381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67236069 | GAGGAATCTAAAAGG[A/G]TACATCCCAGCCTGC | 22992 |
rs191366981 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | KDM2A | GRCh38.p7 | 11:67138447 | CCAGTTGTTTTCAAA[A/G]TGTGCTCCCCAGACC | 22992 |
rs191372992 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67182242 | TTCCTTCCCCTAAAA[A/G]GAGTAGAGAAATTTC | 22992 |
rs191443260 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67177440 | TTATTCTATAAGCTT[G/T]TGTCTACTAAAGTTT | 22992 |
rs191482949 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67124155 | ACTACAGGTGCCCAC[A/C]ACCACACCCAGCTAA | 22992 |
rs191496647 | snp | A/C | 0.00036543 | 0.0135123 | intron-variant | KDM2A | GRCh38.p7 | 11:67219241 | TCTGAGAGAGACTTA[A/C]TGTAATGTGTGTTTT | 22992 |
rs191502121 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67161204 | TGTCTCTATTAAAAA[A/T]TTTTTTAAATTGAAA | 22992 |
rs191522892 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67196100 | CACGAACATAATTGT[C/T]GGTCATAAATTGAGG | 22992 |
rs191523736 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67142813 | AATTAAAATTAGAAA[A/C]ATTTAAAAAACTTAC | 22992 |
rs191587921 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67216656 | CCAGGCATGGTGGCT[C/T]ACGCCTGTAATCCCA | 22992 |
rs191596356 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KDM2A | GRCh38.p7 | 11:67248801 | TTGTCATCTTCACTT[C/T]TGTGGCCTGGCAGAA | 22992 |
rs191640913 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67243445 | TATCTAAAAGGAGCA[C/G]AGTTTTTCTTTGACG | 22992 |
rs191645841 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67180583 | GATTCCATGCGCACC[A/G]TGCATCTTTGATCCT | 22992 |
rs191651521 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67145794 | ACCTTTGCGTATGCT[C/G]TTCTTTCTGAATCAT | 22992 |
rs191687427 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KDM2A | GRCh38.p7 | 11:67216346 | TTAAGATCTAAACCA[A/G]CTTTCCCTCTATGTA | 22992 |
rs191741693 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67175474 | ATTTTCACACTGTTG[C/G]CAACTTTCCAGTTGC | 22992 |
rs191766123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67240590 | TCCTTTCCCTCTCTG[C/T]CCAGGCACCTTCTGT | 22992 |
rs191788448 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67214062 | ATTTATTTTTTGAGA[C/T]GGCGTTTCGCTCTTG | 22992 |
rs191792016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67166663 | CAAGGAGTTCTGGGC[C/T]GTAATGCAGTATACA | 22992 |
rs191797821 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67249662 | ATTATTCACGTGGGG[G/T]TTGGAGTGGAAGACG | 22992 |
rs191860127 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KDM2A | GRCh38.p7 | 11:67209695 | GTGATCCACCTGTCT[C/T]AGCCTCCCAAAGTGC | 22992 |
rs191865100 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67129505 | TTTGGAAGGCCGAGG[C/T]GGGCGGATCACAAGG | 22992 |
rs191871588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67227219 | ACTACAAAGTATGAG[A/G]CAGGCAAGCTGAGCA | 22992 |
rs191931868 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67162651 | CCTCAAGTGATCCGC[C/G]CGCCTCGGCCTCCCA | 22992 |
rs191939560 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67205541 | CAGGTGATTCTCACA[A/C]CTCACCCTCCCGAGT | 22992 |
rs191956108 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67221830 | ATCCTAGCTACTGGG[C/G]AGGCTGAGGTGAGAG | 22992 |
rs191973772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67200377 | TCCGCCACCACGTCC[A/G]GCTAATTTTTTTCGT | 22992 |
rs191998820 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67131510 | TCTGCCTCCCAGGTT[C/G]AGGCAATTCTCCTGC | 22992 |
rs192016165 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67125848 | ACTCAGGAGGCTGAG[G/T]CAGGAGAATCACTTG | 22992 |
rs192022033 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67187762 | TATTTTTAGTAGAGA[C/T]GGGGTTTTGCCATGT | 22992 |
rs192039985 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67168308 | TATGTGGCTTCTTAG[A/G]TGGAGCTTCCCCCAA | 22992 |
rs192102284 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67209151 | TTGGCCAGGCTGGTC[C/T]TGAACTCCTGACCTC | 22992 |
rs192111042 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67151317 | CTACTATGAATTAAG[A/T]TGTTGGTGTAAACTA | 22992 |
rs192125175 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185630 | GGTGACGAGCGAAAC[C/T]CTGTCGCAAAAAAAA | 22992 |
rs192158910 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67135090 | TTTTTCCCCCTGAGA[C/G]GGAGTTTCACTTTTG | 22992 |
rs192173504 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67171541 | ACAGCAAAGTAATAG[A/G]AAAAGTGACACCAGA | 22992 |
rs192182798 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | KDM2A | GRCh38.p7 | 11:67191275 | CGTGATCTGCTCGCC[C/T]CGGCCTCCCAAAGTG | 22992 |
rs192188356 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67157127 | GACCATCCTGGCTAA[C/T]ACGGTGAAACCCCGT | 22992 |
rs192193035 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67228831 | AACCTCAAACTCCTG[A/G]GCTCAAGCAATCCCC | 22992 |
rs192197302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67192958 | TTCACTCAAATACTT[A/G]ATATTATGAGATATT | 22992 |
rs192244179 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67126323 | CTCACACCTATATTC[C/T]CAGCACTTCGGGAGG | 22992 |
rs192332132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67188309 | AACACGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 22992 |
rs192340923 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67214112 | GTGGCACCATCTCGG[A/C]TCACCAGAACCTCCA | 22992 |
rs192343583 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67154192 | ATAGAGGTGAACTAC[A/G]ACCCATGTACCAAAT | 22992 |
rs192352650 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67256545 | CCCCGCCTTTTGGTC[A/G]TCCATCCCTGTCCCT | 22992 |
rs192598717 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67233030 | CTATCTAAACTGGAG[A/G]AAATTATTTTAAGTC | 22992 |
rs192599448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67211151 | CCCCCCATAGTATAT[C/T]CCTTCATTTATCTAG | 22992 |
rs192605177 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67250818 | GCAGGGATTCAGGGG[G/T]TCAGGAATTAGGGGT | 22992 |
rs192614350 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67257205 | ATCCACAGAAATTTC[C/T]AAGCCAATGGTTTCT | 22992 |
rs192637375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67148248 | ACAACATTGCAAGAC[C/T]GCATCTCTATTAAAA | 22992 |
rs192644437 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67143655 | TTTATTTTTTTGAGA[C/T]AGGGTCTCACTCCAT | 22992 |
rs192644733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67161811 | AGACTTTCCAGAAGT[A/G]TAGTAGAGGTTTCTA | 22992 |
rs192663744 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67172450 | ACCATTTAATTTCCT[C/T]CAACAATGCTTTGTA | 22992 |
rs192676397 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67197074 | GCCCTTTGTAACCTT[C/G]TATTTTCTAAATAAA | 22992 |
rs192689267 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67214450 | ACCTCGTGATCCACC[C/T]GCCTCGGCCTCCCAA | 22992 |
rs192692802 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67177667 | TTTTGGATACCTCCT[A/T]AGAGACCTCCCTGAG | 22992 |
rs192716645 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67169112 | AGGCGCCTGCCACCG[C/T]GCCTGGCCAATTTTT | 22992 |
rs192722217 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67196737 | AATGGGGACTTAAAA[C/T]GGCCATAGTTTCAGT | 22992 |
rs192734535 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67232222 | TTCAGGCTGACCCCA[A/G]AAATAAAGTGACCCA | 22992 |
rs192762741 | snp | A/G | | | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67238467 | AGCCTTTCAAACAAA[A/G]TAAGCCGATTGCAGT | 22992 |
rs192781219 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67171821 | CTGCTCCTGGTCTTG[G/T]CATGCTTACTGAAAA | 22992 |
rs192788435 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67135383 | TTTCCTTTTGATACT[C/G]TCTTTGAAGGATAGG | 22992 |
rs192864524 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67161125 | CCCACACTTTGGGAG[A/G]CCAAGTTGGGAGGAT | 22992 |
rs192891157 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67123524 | TAACTTTTCTTTGGG[A/T]ACAGAAAAAGAGATG | 22992 |
rs192904328 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67182834 | CACTGCACCCGGCTG[A/G]AATAAAGTCTTTTTG | 22992 |
rs192918750 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67217485 | GGTCCCTCTTCTCTC[C/G]GAGTCCTGGATGGTG | 22992 |
rs192946237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67148523 | ACAAGTAATCCGGCC[A/G]GGCGTGGTGGCTCAT | 22992 |
rs192963868 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67217680 | TCAGTTGAGGGAGAC[C/G]ACTGGGTCATGTCAA | 22992 |
rs192996581 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67157427 | TTTATTTTTTAAAAG[C/G]AAAAAAATTCCTGGT | 22992 |
rs193006154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67191806 | GCTTTTACTGCCTCT[A/G]TTCAATGTAGCACTG | 22992 |
rs193016519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67130701 | TTTATCTCACTTTTG[A/G]AATAATACTTTATTT | 22992 |
rs193044503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67242473 | TGAGAAATGAAGGCA[A/G]TTACCTGATAATATT | 22992 |
rs193067096 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67141661 | GACAGAATGAGACTC[A/G]TTCCAAAAAAAAAAA | 22992 |
rs193141551 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67204962 | TAGTGCTGCAGTGAA[C/T]ATTTATGTACAAGCT | 22992 |
rs193144133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67167653 | GAGACTTAGGTACGC[A/G]TAAGCTTCCTGCTAA | 22992 |
rs193156917 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67201565 | CACAAGTCAGGGGTA[C/G]AAGACCAGCCTGACC | 22992 |
rs193158955 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67164478 | TGCTATTGGCCTTTT[G/T]TTGTTGTTGTTGTTT | 22992 |
rs193166964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67237074 | CTTAATTCACCAGCT[A/G]ATAAACTTTCCTGTT | 22992 |
rs193178222 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67126762 | TTATTTACCTATTAC[A/G]TGTGGAAAAGAAATG | 22992 |
rs193211982 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67153060 | CACGATCTCAGCTCA[A/C]TGCAACGTCTGCCTC | 22992 |
rs193290965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | KDM2A | GRCh38.p7 | 11:67186549 | GACATTAGATTGTAA[C/T]TTGAAGCCATATGAA | 22992 |
rs193294051 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67124896 | AGAGTCTTGCTCTGT[C/T]GCCCAGGCTGGAGTG | 22992 |
rs193298197 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67221282 | GAATACTAAGCTAGT[A/G]TGGAGATGAGCAGAT | 22992 |
rs199511730 | snp | A/T | 0.000949691 | 0.0217702 | intron-variant | KDM2A | GRCh38.p7 | 11:67253637 | GACCTGACTTCTCTG[A/T]GCTTGTCTTGGGGTA | 22992 |
rs199528075 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67223384 | TTTTCTTCCTTTTTT[C/T]TTTCTTATTTATTTA | 22992 |
rs199555384 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67221019 | TACCTGTCTGACCCG[-/A]AAAAAAAAAAAAAAG | 22992 |
rs199567529 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67153830 | AAAAAAAAAAAAAAA[-/A]CACCAAAAACAACCA | 22992 |
rs199579214 | in-del | -/CT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67122358 | TGAGATTGAGTCTCA[-/CT]CTGTCGCCCACGCTT | 22992 |
rs199618132 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67122647 | TTTTTATTTATTTTT[A/T]TTTATTTATTTATTT | 22992 |
rs199633970 | in-del | -/ATATATATATATATA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67247057 | TATATATATATATAT[-/ATATATATATATATA]TTTTTTTTTTTTTTT | 22992 |
rs199668887 | in-del | -/TG | 0.0689305 | 0.172377 | intron-variant | KDM2A | GRCh38.p7 | 11:67129901 | GGGCGACAGAGACTC[-/TG]TCTCAAAAAAAAAAA | 22992 |
rs199675415 | snp | A/G | 1.65971e-05 | 0.00288067 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67180101 | CCATGCGACGACGCT[A/G]TGAAGATGATGGCAT | 22992 |
rs199718565 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67222085 | TTTTTTTTTTAATTT[A/T]TTTTTTTATTGATAA | 22992 |
rs199740896 | snp | A/C | 1.6631e-05 | 0.00288362 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67245440 | GAAGCAGTCCTGTGT[A/C]CTCCGACAGTGCTTG | 22992 |
rs199801264 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67237000 | CTGGCATGACACAGG[A/C]CACAGAGAAAATGAG | 22992 |
rs199852243 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67205439 | TAATGCTACCTGATA[C/T]ATCCAGCCAGGGCAG | 22992 |
rs199857566 | snp | A/G | 3.31334e-05 | 0.00407009 | intron-variant | KDM2A | GRCh38.p7 | 11:67228181 | AAGTATTCTGCCTAT[A/G]GGAGCTTTGAAGACA | 22992 |
rs199878701 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67222059 | TTTAACTCTGTCATT[C/T]TTTTTTTTTTTTTTT | 22992 |
rs199898690 | in-del | -/ATTATC | | | intron-variant | KDM2A | GRCh38.p7 | 11:67237453 | TTCTTTATTATTATT[-/ATTATC]ATTATTATTATTATT | 22992 |
rs199904630 | in-del | -/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67215673 | TTAGTCAATACGGTA[-/G]GAAAAAAAAAAAACC | 22992 |
rs199919971 | in-del | -/TTTA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67187549 | ATTTATTTAATTGAT[-/TTTA]TTTATTTATTTATTT | 22992 |
rs200007669 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67203439 | TCTATAATAAATAAT[A/T]TATTAATATAATTAT | 22992 |
rs200011930 | snp | A/G | 0.000132668 | 0.00814348 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67231773 | CTTCTGACTGTAGCC[A/G]GGGCTCCCACAATGG | 22992 |
rs200017523 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67125462 | TCATTTTTTGGGGGG[-/A]AAAAAAAATCAGAAA | 22992 |
rs200062952 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67142004 | AATGACAGAATTTCA[C/T]TCTTTTTTATGGATG | 22992 |
rs200078110 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67184105 | CCTGTCTCAAAAAAA[A/G]AAAAAAAAAAGGCAG | 22992 |
rs200120639 | in-del | -/AC | | | intron-variant | KDM2A | GRCh38.p7 | 11:67129429 | CCCGTCTCTACTAAA[-/AC]AATACAAAAATTAGC | 22992 |
rs200125254 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67193236 | CTCAGGTGATCCACC[C/T]GCCTCAGCCTCCCAA | 22992 |
rs200130297 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67158967 | CCCAGTGAGTGGCTT[G/T]TCTTTTCATTCCTTT | 22992 |
rs200139765 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67129902 | GGCGACAGAGACTCT[C/G]TCTCAAAAAAAAAAA | 22992 |
rs200143814 | snp | C/T | 0.000364293 | 0.0134912 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | KDM2A | GRCh38.p7 | 11:67215871 | GTACTGTCTAATGAG[C/T]GTTCGAGGCTGCTAT | 22992 |
rs200150872 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67242280 | TGTGGGTGTGTGTAT[A/G]TGTGTGTGTGTGTGT | 22992 |
rs200176455 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67235429 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 22992 |
rs200176527 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67169763 | TCTCTCTCTCTCTTT[C/T]TTTTTTTTTTTTGAG | 22992 |
rs200210620 | in-del | -/TTTGT | 0.0816945 | 0.18486 | intron-variant | KDM2A | GRCh38.p7 | 11:67198760 | AGTGGTGATCAGTAG[-/TTTGT]TTTGTTTTGTTTTGT | 22992 |
rs200212765 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67145983 | TCTTCCCGTTTTTTG[-/T]TTTTGTTTTTTTTTG | 22992 |
rs200222997 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67201217 | AAATATATATATATA[C/T]ATGTGTGTGTGTGTG | 22992 |
rs200231510 | in-del | -/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67200216 | TAATATTGTTTGTGT[-/G]GTTTTTTTTTTTCTT | 22992 |
rs200250329 | snp | A/C/G | 0.00013275 | 0.0081461 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67245413 | GAAGAAGTTTGGGGG[A/C/G]CCTGGACGCATGAAG | 22992 |
rs200253663 | in-del | -/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67179259 | ATTTGGAATGCTGGG[-/T]TTTTTTTTGTTTTGT | 22992 |
rs200258064 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67146072 | TCTCAGCTCACTGCA[A/G]CCTCCACCTCCCGGG | 22992 |
rs200263280 | snp | A/G | 1.66081e-05 | 0.00288163 | utr-variant-5-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67121316 | AACAGAAGAGTGAGA[A/G]ATGGAACCCGAAGAA | 22992 |
rs200417175 | in-del | -/GTTT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67124009 | GTTGTTTGTTTGTTG[-/GTTT]GTTTGTTTTGAGACT | 22992 |
rs200428208 | in-del | -/A | 0.0185938 | 0.0946107 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206392 | CAAGATTTCGCACCA[-/A]CTGCACTCCAGCCTG | 22992 |
rs200451328 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206574 | AACCCCGTCTCTACT[-/A]AAAATACAAAAAATT | 22992 |
rs200465239 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67172620 | AGCTCTTATAGTTGT[G/T]TGTGTGTGTGTGTGT | 22992 |
rs200466687 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67163855 | GCGACACTCCATCTT[-/A]AAAAAAAAAAAAAAA | 22992 |
rs200511017 | snp | G/T | 0.00299544 | 0.0385843 | intron-variant | KDM2A | GRCh38.p7 | 11:67179880 | TTCATAGAGGACCCA[G/T]TGGCTCATTGAAACT | 22992 |
rs200549212 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67203437 | AGTCTATAATAAATA[A/T]TATATTAATATAATT | 22992 |
rs200577775 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67162992 | TGGGATTATAGGCTT[A/C]AGCCACCAAGCGTGG | 22992 |
rs200586109 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67223388 | CTTCCTTTTTTCTTT[C/T]TTATTTATTTATTTA | 22992 |
rs200595292 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67147639 | AGAATTTCAAGGATC[A/G]AGGGCTTTCTCTGGA | 22992 |
rs200605538 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67122231 | ATGGTGGTTTTATTT[A/C]GCTCTGCATTTTAGA | 22992 |
rs200660138 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67203019 | AAAAAAAAAAAAAAA[C/T]AAAAACGGTTTACAC | 22992 |
rs200660924 | snp | A/G | 0.000135478 | 0.00822927 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | KDM2A | GRCh38.p7 | 11:67207610 | GACCCCAGAGGAGGA[A/G]CGAGAGAAACTCTAT | 22992 |
rs200685678 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67235161 | AAAAAAAAAAAAAAA[C/T]AAAAAAGAAAGGAAG | 22992 |
rs200740596 | in-del | -/AGG | | | intron-variant | KDM2A | GRCh38.p7 | 11:67175621 | AAATGGAAGAATTTA[-/AGG]AGAAGAAAAGCATGA | 22992 |
rs200744093 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67219558 | CAAAATTTTAAATTT[-/A]ATTTTTTTTTTTTTA | 22992 |
rs200744426 | snp | G/T | 0.000100497 | 0.00708792 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67250307 | TGAGCGCTTCAAACG[G/T]CGGCAGTTGCTGCGG | 22992 |
rs200805069 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67222093 | TTAATTTATTTTTTT[A/T]TTGATAATTCTTGGG | 22992 |
rs200831428 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67169759 | TCTCTCTCTCTCTCT[C/T]TTTTTTTTTTTTTTT | 22992 |
rs200841610 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67176952 | TTTTAATTTATAAAA[-/T]TTTTTTTTTTCAATA | 22992 |
rs200866980 | in-del | -/ATTT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67122690 | TTTATTTATTTATTT[-/ATTT]TTTGAGACAGAGTCT | 22992 |
rs200898314 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67194461 | TCTTAAGTTATGTTA[C/T]CTAGTCAGTTGATCA | 22992 |
rs200949810 | in-del | -/ATATATAT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67141683 | AAAAAAAAAAAAAAA[-/ATATATAT]ATATATATATATATA | 22992 |
rs200961023 | in-del | -/AAAAAA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67129734 | GCGAGACTCCATCTC[-/AAAAAA]AAAAAAAAAAAGAAA | 22992 |
rs200974599 | in-del | -/C | 0.0803491 | 0.183626 | intron-variant | KDM2A | GRCh38.p7 | 11:67223384 | TTTTCTTCCTTTTTT[-/C]TTTCTTATTTATTTA | 22992 |
rs200977410 | in-del | -/ATATATA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67247065 | TATATATATATATAT[-/ATATATA]TTTTTTTTTTTTTTT | 22992 |
rs200991467 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67154535 | CCTCCTGGGTTCAGG[C/T]GATTCTCCTGCCTCA | 22992 |
rs200996327 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67170387 | CCTACCAAGCATGGG[G/T]TTTTTTTTTTTTCTT | 22992 |
rs201038643 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67192433 | ACTTTGTTTCCATTT[C/T]TTTTTTTTTTTTTTT | 22992 |
rs201100651 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67203463 | TAATTATATTTATTA[A/T]TTATTAATAATTATT | 22992 |
rs201128327 | in-del | -/TTGTTTTG | 0.0752517 | 0.178782 | intron-variant | KDM2A | GRCh38.p7 | 11:67198776 | TTGTTTTGTTTTGTT[-/TTGTTTTG]TTTTGTTTTGTTTTT | 22992 |
rs201135588 | snp | A/G | 0.000899685 | 0.0211904 | intron-variant | KDM2A | GRCh38.p7 | 11:67217708 | CAATGGCTGTTAACA[A/G]ACTAAAGTTTTTTAA | 22992 |
rs201167901 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67217313 | AAGTCATTTTGTTTG[C/T]TTCAGATCCCTTTAA | 22992 |
rs201174411 | in-del | -/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67204495 | TGTGTTTTCTTTTTT[-/C]TTTTTTTTTTTTTTG | 22992 |
rs201251880 | in-del | -/AAT | 0.455263 | 0.142713 | intron-variant | KDM2A | GRCh38.p7 | 11:67203433 | AAATAGTCTATAATA[-/AAT]AATATATTAATATAA | 22992 |
rs201286401 | snp | G/T | 3.65778e-05 | 0.00427639 | intron-variant | KDM2A | GRCh38.p7 | 11:67232004 | TACTGATCCAGCTAT[G/T]GCAGTCAGCTTCCAG | 22992 |
rs201292782 | snp | C/T | 0.000646214 | 0.0179636 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67245383 | GTGTGGTGTTTGCCA[C/T]TACTGCAGAGACATG | 22992 |
rs201296173 | snp | C/G/T | 0.000154582 | 0.00879043 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67207490 | CTCGATAGAGATGAT[C/G/T]GATGCATCTTTTATG | 22992 |
rs201314470 | in-del | -/T | | | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67238443 | ATAGCTAGATCACTG[-/T]TTAAGGAAAGCCTTT | 22992 |
rs201314767 | snp | A/C | 4.97789e-05 | 0.00498868 | missense, intron-variant | KDM2A | GRCh38.p7 | 11:67250497 | AAGCTGCAGGCCATC[A/C]CGGCCTCCTCTGCCA | 22992 |
rs201337168 | snp | A/G | 0.000221218 | 0.0105148 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67250169 | CGATGAGCCTCTCAC[A/G]CCCCCGCCTCATTCA | 22992 |
rs201363212 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67196903 | ATTTTTTACAAGTTG[-/A]AAAAAAAAATAGACT | 22992 |
rs201384231 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67242303 | GTGTGTGTGTGTGTG[A/T]GAGAGAGAGAGAGAA | 22992 |
rs201406330 | in-del | -/A | 0.180383 | 0.240111 | intron-variant | KDM2A | GRCh38.p7 | 11:67148259 | GACCGCATCTCTATT[-/A]AAAAAAAAAAATTTA | 22992 |
rs201434394 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67222080 | TTTTTTTTTTTTTTT[A/T]ATTTATTTTTTTATT | 22992 |
rs201451944 | snp | A/T | 0.0197687 | 0.0974348 | intron-variant | KDM2A | GRCh38.p7 | 11:67122645 | ATTTTTTATTTATTT[A/T]TATTTATTTATTTAT | 22992 |
rs201500981 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67169761 | TCTCTCTCTCTCTCT[C/T]TTTTTTTTTTTTTTG | 22992 |
rs201504546 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67219572 | AATTTTTTTTTTTTT[-/T]AAGGCAGAATCTTGT | 22992 |
rs201548514 | in-del | -/A | 0.00597247 | 0.0543191 | intron-variant | KDM2A | GRCh38.p7 | 11:67157428 | TTATTTTTTAAAAGC[-/A]AAAAAATTCCTGGTT | 22992 |
rs201555610 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67221036 | AAAAAAAAAAAAAGG[A/T]AAAAAACACTCCTAG | 22992 |
rs201573988 | in-del | -/GT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67170387 | CCTACCAAGCATGGG[-/GT]TTTTTTTTTTTCTTT | 22992 |
rs201622499 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67120072 | TCCCCCTCCCCCCCC[-/T]CATTTGGAAGTTTGG | 22992 |
rs201656775 | snp | A/T | 1.65638e-05 | 0.00287778 | intron-variant | KDM2A | GRCh38.p7 | 11:67215960 | GAAAGGTATGGTCAT[A/T]GTTGTGATAGGGGTT | 22992 |
rs201729958 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67203438 | GTCTATAATAAATAA[A/T]ATATTAATATAATTA | 22992 |
rs201740869 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67141688 | AAAAAAAAAAATATA[A/T]ATATATATATATATA | 22992 |
rs201783911 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67145998 | GTTTTGTTTTTTTTT[G/T]TTTTTTTTTTTTGAG | 22992 |
rs201838420 | in-del | -/GGGGTT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67142557 | GGTGAAGTTGGCCGG[-/GGGGTT]GGGGTTGGGGTTGGG | 22992 |
rs201869182 | snp | G/T | 0.00182202 | 0.0301279 | intron-variant | KDM2A | GRCh38.p7 | 11:67219439 | GTTGCATGTGAAGAG[G/T]TTTACTCCAGTTATG | 22992 |
rs201937858 | snp | A/G | 0.000413938 | 0.0143805 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67228119 | ACTGCATAACCAACC[A/G]TTCCCACCTAACTAA | 22992 |
rs201941702 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67198317 | TTTGCAGATAGTGTA[-/T]TTTTTTTTTTTTTTA | 22992 |
rs201948496 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67233654 | TGAAACCCTGTCTCA[A/T]CAACAACAACAACAA | 22992 |
rs201958092 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67155858 | CGACCTCAGGTGATC[C/T]GCCTGCCTCGGCCTC | 22992 |
rs201963300 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67151259 | GTGTTGTACGCTATG[G/T]TAGCCACTAGCCACA | 22992 |
rs201996361 | snp | C/T | 0.000132492 | 0.00813809 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67254375 | TCTACTCACTGCTGT[C/T]GGGTCTTCCACTCGC | 22992 |
rs202015878 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67123144 | CAGGGTAATTTTCAG[-/A]CTTTTTTTTTTCTTA | 22992 |
rs202025193 | snp | C/T | 6.64871e-05 | 0.00576534 | missense, intron-variant | KDM2A | GRCh38.p7 | 11:67250350 | GAGCGCACCATGGTA[C/T]GGGAAAAGGAGAACA | 22992 |
rs202026812 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67131137 | CAAGACCAGCCTGGC[C/T]AACATGACGAAACCC | 22992 |
rs202130695 | in-del | -/T | 0.00438332 | 0.0466095 | intron-variant | KDM2A | GRCh38.p7 | 11:67167622 | CCTACTGACTAAATA[-/T]TTTTTTTTTAATCAA | 22992 |
rs202144734 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67174236 | GCACTCCAGCCTGGG[C/T]GACAGAGTAAGACTC | 22992 |
rs202195285 | in-del | -/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67177453 | TTTTGTCTACTAAAG[-/T]TTTTTTTTTAACTTT | 22992 |
rs202214740 | snp | A/G/T | 6.62475e-05 | 0.005755 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67231818 | CCCAGTGTGCTCCCC[A/G/T]AAAGGACAGGCAAGT | 22992 |
rs202236882 | in-del | -/TAAA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67150579 | TGGAAACCACTTGTT[-/TAAA]TAAGGGAATATCAAG | 22992 |
rs367554522 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67192423 | ATGGACATTTACTTT[G/T]TTTCCATTTCTTTTT | 22992 |
rs367629572 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67218481 | GGCCTCATGCAGCCC[A/G]GGATGGCTTTGAATG | 22992 |
rs367632212 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67241562 | AATTATTAGCAATGG[C/T]CCAGACTTGCTAACC | 22992 |
rs367648085 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67244986 | GCGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 22992 |
rs367710437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67233170 | AATCTACAAGTTGTA[A/G]TGTTATTTTGAAAAC | 22992 |
rs367715108 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67223540 | CCTGAGTAGCTGGGA[C/T]CACAGACGCACACCA | 22992 |
rs367715261 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67163853 | GAGCGACACTCCATC[C/T]TAAAAAAAAAAAAAA | 22992 |
rs367747123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67141592 | GAATGGCGTGAACCC[A/G]GGAGGCAGAGCTTGC | 22992 |
rs367751265 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67121573 | TTGGAAATGGAGTTA[C/T]ATGTAGCCTTTAGCT | 22992 |
rs367766697 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | KDM2A | GRCh38.p7 | 11:67200378 | CCGCCACCACGTCCG[C/G]CTAATTTTTTTCGTA | 22992 |
rs367770448 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67133067 | CTTGAGTTTTAGTAT[C/G]AAGTCTCTTACCAAT | 22992 |
rs367777129 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67184321 | CAACATGGGGAAACT[A/C]CATCTCTACTAAAAA | 22992 |
rs367778242 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67256534 | CCCCCACCCCGCCCC[A/G]CCTTTTGGTCGTCCA | 22992 |
rs367857368 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67207983 | CTGCAGTGACCGGTG[A/G]TTGCACCACTGCATT | 22992 |
rs367874956 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67134077 | TTGAAGGCAAAGACA[A/T]ATGAAATACTAAGGT | 22992 |
rs367881055 | snp | G/T | 4.98824e-05 | 0.00499387 | intron-variant | KDM2A | GRCh38.p7 | 11:67181831 | CATATATACTTACTG[G/T]TGTTTGTTTCATAGA | 22992 |
rs367894222 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67235864 | ACCTTGCGATCCACC[C/T]GCCTTGGCCTCCCAA | 22992 |
rs367899015 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67224347 | TGGTGGTTCATGCCT[A/G]TAATCCCAAGTACTT | 22992 |
rs367901892 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67175635 | AAGGAGAAGAAAAGC[A/G]TGAAAAAGATCAGGG | 22992 |
rs367903384 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67250992 | TGTCATTAGGGAACT[A/G]GCCATTTGCCTCCTG | 22992 |
rs367906544 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67181593 | AAATATAGATGAACC[-/A]AAAAAAAAAAAAACA | 22992 |
rs367910857 | snp | A/C/G | 6.71404e-05 | 0.00579365 | intron-variant | KDM2A | GRCh38.p7 | 11:67181796 | AAAAAACTCACATTT[A/C/G]CTAGAGCAATTGTGT | 22992 |
rs367962812 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67190148 | AGCGCGGTGGCTGAC[A/C]CCTATAATCCCAGCA | 22992 |
rs367999093 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67125198 | TTTTCTTTTTTTTTT[A/T]TTTGAGATAGGGGTC | 22992 |
rs368007948 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67147369 | AACACGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 22992 |
rs368020851 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67222866 | ATCCCCTGCATGAAG[A/G]GTTTTCTACGTAAAG | 22992 |
rs368030760 | in-del | -/CA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67168492 | TTTAATTTTTGTATA[-/CA]GAGTGTCTGGCTATT | 22992 |
rs368037059 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67149722 | CTAGGTATTAGAATC[-/T]TTTTTTTTTTTTTTT | 22992 |
rs368039335 | in-del | -/AGC | | | intron-variant | KDM2A | GRCh38.p7 | 11:67202814 | GTCGACCCGAGAAAC[-/AGC]GAGATCTTGTATCGG | 22992 |
rs368043782 | snp | C/T | 0.000161987 | 0.00899819 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67250343 | GGCCACAGAGCGCAC[C/T]ATGGTACGGGAAAAG | 22992 |
rs368096489 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67183533 | CTGTCTGATACAACT[A/G]TTTTGGAGTTCAGGA | 22992 |
rs368110706 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67216180 | ACTTAGTAAATCTCA[A/G]TAGTCCTGTTTCTAG | 22992 |
rs368141431 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67156108 | TACAAAATAGCTGTG[C/T]GTGGTGGCACATGCC | 22992 |
rs368146204 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67216944 | AACAAACAACAACAA[A/C]AAAAAAACATGAGGT | 22992 |
rs368148624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67230004 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 22992 |
rs368178208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67160495 | TAGATCTTCTGGGCC[A/G]GGTGCGATGTTCACA | 22992 |
rs368182213 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67201859 | ATTTGGGTGGCTGAG[C/G]TGGGAGGATCACTTG | 22992 |
rs368269222 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67233419 | AGCACTTTGGGAGGC[C/T]GAGGCAGGTAGATCA | 22992 |
rs368279928 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67235276 | GAAAGTGTACATAGG[C/T]AGAATAGGGTTTTCC | 22992 |
rs368282139 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67215517 | CAAGGATTGGCTTCT[C/T]CCTTACGAGCTTTGC | 22992 |
rs368286910 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67202938 | AGTTTGTGGCTGTGG[G/T]GAGCTGTGATTGCAC | 22992 |
rs368288250 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67184213 | TAAAGGGCTATTGTG[A/G]CCGGGTGCAGTGGCT | 22992 |
rs368340466 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67126212 | GATCATGCCGTTGCA[A/C]TCCAGCCTGGGGAAC | 22992 |
rs368358428 | in-del | -/TTTATTTA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67218598 | ATTAGTATATTTTAT[-/TTTATTTA]TTTATTTATTTATTT | 22992 |
rs368375687 | snp | A/T | 0.000127111 | 0.00797114 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67231630 | GGATCGAGAACCCCG[A/T]CGCTTGAGCAGCAGG | 22992 |
rs368415659 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67183919 | TTTGAGATCAGCCTG[C/G]GCAACATAGCAAGAC | 22992 |
rs368424539 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67240512 | GTTGCTTGAGCCGTC[A/G]TTGCACTTGTTCCCT | 22992 |
rs368429388 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67208194 | AATAACTGCATTTTC[C/T]GAAATCATAATAAAT | 22992 |
rs368432826 | in-del | -/GTTTTGTTTT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67235629 | GTTTTGTTTTGTTTT[-/GTTTTGTTTT]TGAGACAGAGTCTTG | 22992 |
rs368510719 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | KDM2A | GRCh38.p7 | 11:67133236 | TCCCAGGTAGCTGGG[A/G]TTACAGGCGTGCGCC | 22992 |
rs368528427 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67228759 | TTTTTGTTTTAGAGA[C/T]AGGGCCTTGCCCTGT | 22992 |
rs368533931 | in-del | -/TTCTTTT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67139256 | TTCCTTTTTTCTTTT[-/TTCTTTT]GAGACGGAGTCTCGC | 22992 |
rs368536747 | snp | A/G | 6.62482e-05 | 0.00575497 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67245302 | AGCTGCTGCCTCCCC[A/G]ATTGTGTCAGGAGCC | 22992 |
rs368584015 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67199382 | ATGTCAAAAGCCAAG[A/G]TAGGCCTTTTACATC | 22992 |
rs368587627 | snp | C/G | 0.000155988 | 0.00883003 | synonymous-codon, intron-variant | KDM2A | GRCh38.p7 | 11:67250733 | GGTCTGGATGTCTGT[C/G]TTCCGCTACCTCAGC | 22992 |
rs368587739 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67139976 | TCCACAGTGTTGGAA[C/T]TATAGGCGTGAGCCA | 22992 |
rs368604712 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67214582 | GACCTCAGGTGATCC[A/G]CCTGCCTTGGCCTCC | 22992 |
rs368620489 | in-del | -/A | 0.00199481 | 0.0315187 | upstream-variant-2KB, utr-variant-3-prime | KDM2A, LOC107984341 | GRCh38.p7 | 11:67117477 | TTACGTAGCGCTTTT[-/A]CCTTGGAGTTCAAGC | 22992 |
rs368640858 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67202626 | AAATACAAAAAAAAA[-/A]CTAGCCAGGCATGGT | 22992 |
rs368643179 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67208788 | AAAAAAAAAAAAAAA[C/T]TCACTCTTGACCAGG | 22992 |
rs368648318 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67128836 | ACACATAGCAAGTGC[C/T]GAATAAGTATTTGTT | 22992 |
rs368651081 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67235801 | ATTTTTGTATTTTTA[C/G]TAGAGACGGGGTTTC | 22992 |
rs368683805 | snp | A/G | 1.68179e-05 | 0.00289977 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67250217 | GCTCATCCATGACCC[A/G]GTTTCCCCCCGGGGT | 22992 |
rs368687199 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67155987 | GGGCGCAGGGCTCAC[G/T]CCTGTAATCCCAGCA | 22992 |
rs368728916 | snp | A/T | 0.000161987 | 0.00899817 | intron-variant | KDM2A | GRCh38.p7 | 11:67253614 | GCTGATAAACCAGGT[A/T]TGCTCTGGACCTGAC | 22992 |
rs368737787 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67144173 | TGGTCTCAAACTCCT[C/G]ATGTCACGTGATCTG | 22992 |
rs368740068 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67170833 | CTTGACAATTTCTTC[C/G]GGTTACCTTAAGAGA | 22992 |
rs368749649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67202993 | GAGCAAGACCCTGTC[C/T]GTCCGCCGCCAAAAA | 22992 |
rs368761787 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67168586 | TGTATGAATTATACA[C/T]ACACACACACACACA | 22992 |
rs368777707 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67133423 | TATTTTTTGTTTTGA[G/T]ACAGAATCTCACTCT | 22992 |
rs368797016 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67191049 | GAGGGAACACTTCTT[A/T]TTTTTCTTTTTTTGA | 22992 |
rs368798672 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67244384 | GGAGTACTAAAGAAA[C/T]GAACAAGACTAGTTT | 22992 |
rs368849359 | snp | C/T | 9.96181e-05 | 0.00705685 | intron-variant | KDM2A | GRCh38.p7 | 11:67181901 | TGTGTGGGTAAGTGT[C/T]GAGCTTTTGGCCTCT | 22992 |
rs368944105 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67224036 | CATTAGAAAACTGAT[C/T]GGGGCTAACTATGAA | 22992 |
rs368965019 | snp | A/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67205990 | TTTGTTTTTACTGCC[A/G]CTTGAGCACCTACTT | 22992 |
rs369012408 | snp | A/G | 1.65913e-05 | 0.00288017 | intron-variant | KDM2A | GRCh38.p7 | 11:67254426 | TATGGCAGGTATGCC[A/G]CTACAGTTGTTCATA | 22992 |
rs369064848 | snp | C/T | 6.64463e-05 | 0.00576357 | intron-variant | KDM2A | GRCh38.p7 | 11:67245964 | TCAGTTCTCTTGGAT[C/T]CTATCTTTGTCCTCT | 22992 |
rs369084623 | snp | C/T | 0.000376081 | 0.0137076 | intron-variant | KDM2A | GRCh38.p7 | 11:67196475 | TAAAATGTAGCAACC[C/T]AAATGTCCATCAGCA | 22992 |
rs369092079 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67226723 | CAAGACTCCGTCTCA[A/G]AAAACAAACGAAAAT | 22992 |
rs369112604 | snp | C/G | 1.65614e-05 | 0.00287757 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67254335 | ACCTCAGTCACTGCA[C/G]CCACCTTACAGATCA | 22992 |
rs369117347 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67247392 | ACCGCACCCAGCCTG[A/G]TTCTTAGGATATTTT | 22992 |
rs369124261 | snp | C/T | 0.000143493 | 0.0084691 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | KDM2A | GRCh38.p7 | 11:67207640 | TAATGTCATCAGCCT[C/T]GAGTTTAGCCACACC | 22992 |
rs369135143 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67148494 | TCAATCATATCTTTT[A/T]TCCCCCATCAGAAAC | 22992 |
rs369169010 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67124064 | GCTGGAGTGCAATGG[C/T]ACTATCAGGGCTCAC | 22992 |
rs369181311 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67165639 | AGCAAAGCTGGAAAA[C/T]AGGTGCATTTATAGA | 22992 |
rs369194367 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67214223 | TTTTTTTTTTTTTTT[G/T]AGACGGAGTCTTGCT | 22992 |
rs369243029 | snp | A/C | 3.46675e-05 | 0.00416323 | intron-variant | KDM2A | GRCh38.p7 | 11:67252677 | ATGAAGGCGAGTTCT[A/C]TTCCCTTCTATCACA | 22992 |
rs369248041 | in-del | -/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67184787 | AGACGTAAGAAAACT[-/T]AAGTGTATACCTCAG | 22992 |
rs369249907 | snp | C/G | 0.000167986 | 0.00916323 | intron-variant | KDM2A | GRCh38.p7 | 11:67180248 | GTTCCAGCTTACAGT[C/G]CTTTGATGTGGGAAG | 22992 |
rs369284982 | snp | A/G | 3.599e-05 | 0.0042419 | intron-variant | KDM2A | GRCh38.p7 | 11:67248277 | CATCTCTGTCTTCCT[A/G]TAGATGGACGGAGAG | 22992 |
rs369298523 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67201429 | TGGATCCCTTGAGGC[C/T]AGGAGTTTGAGACCA | 22992 |
rs369326090 | in-del | -/TTTGT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67198759 | AGTGGTGATCAGTAG[-/TTTGT]TTTGTTTTGTTTTGT | 22992 |
rs369345892 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67209775 | ATTTAAAAATAACAG[A/G]ATTGGCCACACACGT | 22992 |
rs369354402 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67133971 | TGCTAGGATTAGAGG[C/T]GTGAGCCACCATGCC | 22992 |
rs369358044 | snp | A/C/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67184613 | GCCTGGGTGACAGAG[A/C/G]GAGACTCATCTCAAA | 22992 |
rs369376200 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67256429 | AGGAGATGCTCAGTA[G/T]CAGCAGCCTATGGCA | 22992 |
rs369379497 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67230171 | ACAGAGCGAGACTCC[A/G]TCTCAAAAAAAAAAA | 22992 |
rs369400307 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67174048 | AAATCACCTGAAGTC[A/C]GGAGTTCGAGACCAG | 22992 |
rs369409613 | snp | C/G | 1.65641e-05 | 0.00287781 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67231799 | AATGGACAAGTGTGG[C/G]ATCCCCAGTGTGCTC | 22992 |
rs369410691 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | KDM2A | GRCh38.p7 | 11:67143789 | AGGCGTGTGCCACCA[C/T]GCCCAACTAATTTCT | 22992 |
rs369453382 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67233309 | GGATCACCTGAGGTC[A/G]GGAGTTCGAGACCAG | 22992 |
rs369465688 | in-del | -/TAC | | | intron-variant | KDM2A | GRCh38.p7 | 11:67233362 | CATCTCTACTAAAAA[-/TAC]AAAAAAAGGCTCAGT | 22992 |
rs369466274 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67126720 | TTCAAAAAAAAAAAA[A/T]AAAAAAGTATTTTTT | 22992 |
rs369476041 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67252345 | GCTCCCTTATATACA[C/G]TTCAGCAGGAACCAT | 22992 |
rs369479491 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67213911 | GCCCTGTTGCCCAAG[C/G]TGGAGTGCAGTGGTG | 22992 |
rs369512016 | snp | C/T | 9.96413e-05 | 0.00705767 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67231755 | CTTTGGCTGGGGACT[C/T]ATCTTCTGACTGTAG | 22992 |
rs369569696 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67157475 | TGTGGCCGGGTGCAG[C/T]GGCTCACGCTTGTAA | 22992 |
rs369605898 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67200287 | GTGGCACGATCTCAG[A/C]TCACTGCAAGCTCCA | 22992 |
rs369642369 | snp | A/G | 3.63524e-05 | 0.0042632 | missense, intron-variant | KDM2A | GRCh38.p7 | 11:67250750 | TCCGCTACCTCAGCC[A/G]CAGAGAACTTTGTGA | 22992 |
rs369668797 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67164935 | GTTAGTCAGTTTACC[A/C]CTCTTAGAGTAACTT | 22992 |
rs369702637 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67194384 | ACTCAGATAAAAGTC[C/T]TTCTGAGGCGTAGGT | 22992 |
rs369716655 | snp | A/T | 4.98269e-05 | 0.00499109 | intron-variant | KDM2A | GRCh38.p7 | 11:67121397 | CACCCTCCAGTTTTA[A/T]AGTAGGATAACTATT | 22992 |
rs369735454 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67220721 | AATATTTTAGGCTTC[A/G]TGGGTCATAAAGTGT | 22992 |
rs369772311 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67131557 | GCTGGGATTACAGGC[A/G]TGTGCCACCACGCCT | 22992 |
rs369773729 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67169617 | CTGACCTTAGGTGAT[C/G]CTCCTGCCTCAGCCT | 22992 |
rs369780353 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KDM2A | GRCh38.p7 | 11:67170623 | TTTCACCATGTTAGC[C/T]AGGATGGTCTCGATC | 22992 |
rs369782064 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67230660 | ATAAAAAAAAAAAAC[C/G]CACATAATAATCATA | 22992 |
rs369786810 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67127543 | TTCAATCCTGTTAAC[C/T]TGTCTTACATATAAT | 22992 |
rs369792175 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67156998 | AATTTAAAATATTTA[C/T]CCTCTGGCCCCTTTC | 22992 |
rs369795883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67217071 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 22992 |
rs369827014 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67174854 | TGCAAATTGCTTTTG[A/G]GAGGAAATATGGTTG | 22992 |
rs369838457 | snp | A/G/T | 9.94801e-05 | 0.00705203 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67231776 | CTGACTGTAGCCGGG[A/G/T]CTCCCACAATGGACA | 22992 |
rs369902675 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67253019 | CCAGGGCCATCTTAA[A/G]TGTCAGTCTCCCAGG | 22992 |
rs369913182 | in-del | -/AG | | | intron-variant | KDM2A | GRCh38.p7 | 11:67171492 | AAGTTGAGATCTGAG[-/AG]GTTAAATGATTTATT | 22992 |
rs369914919 | snp | C/T | 3.31763e-05 | 0.00407272 | intron-variant | KDM2A | GRCh38.p7 | 11:67246141 | GCTATGAGGGGTTCC[C/T]GAAGTCTCAGCTAAT | 22992 |
rs369977632 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67192584 | CGAGTAGCTGGGATT[A/G]CAGGCATGCAACACC | 22992 |
rs369978883 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67158096 | TACTGTGCACCACTT[A/G]TTCATCCCCTTTCCT | 22992 |
rs369989215 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67165182 | GCTGGAGTGCAGTGG[C/T]GCGATCTTGGCTCAC | 22992 |
rs369997372 | snp | C/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185827 | ATTCTCTTACTGTCT[C/T]GCTTTTCACCATGTG | 22992 |
rs370007541 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67247833 | AGAATTGGTGAAATA[G/T]GGTATTAATTCCATG | 22992 |
rs370060433 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67149983 | CTCCTCAGCCTCCCA[A/G]AGTGCTGGGATTACA | 22992 |
rs370103679 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67174678 | TATAGTTAATTACGA[C/T]TAAACTGGGAATGGT | 22992 |
rs370114688 | snp | A/C | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206432 | AGCGAGACTGTCTCA[A/C]AATAAAATTAAAGAA | 22992 |
rs370117752 | snp | A/G | 6.5206e-05 | 0.00570953 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67248358 | CCAGGAGGACAGCTC[A/G]GAGAAAGCCCAGGTA | 22992 |
rs370121518 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67234439 | GTGGTAGATGAGATA[A/C/T]TCATAATATTCCAAG | 22992 |
rs370128971 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67243666 | CAAAAATACAAAAAT[A/T]AAGCCAGGCGTGGTG | 22992 |
rs370151839 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67158749 | CTACCTTACATGCCC[A/G]AAGTGCTCGTATTAT | 22992 |
rs370175720 | in-del | -/TAT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67141684 | AAAAAAAAAAAAAAA[-/TAT]ATATATATATATATA | 22992 |
rs370177750 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67212246 | AAGTGGTGCCTAATG[A/T]TGACATAAAAGAAAT | 22992 |
rs370183685 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67153141 | AGGCATGTGCCACCA[C/T]GCCCAGCTAATTTTT | 22992 |
rs370197439 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67214566 | CTGGTCTTGAACTTC[C/T]GACCTCAGGTGATCC | 22992 |
rs370229936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67225922 | ACATAAAAATTAGCT[A/G]GTCATGGTGGTGCAC | 22992 |
rs370324817 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67233338 | AGCCTGGCCAACATG[G/T]TGAAACCCCATCTCT | 22992 |
rs370358741 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67182886 | AAACAAAGGGACTTT[G/T]TAAATTTTCTTCCTA | 22992 |
rs370368107 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67227631 | CTGGAGTGCAGAGGC[A/G]TGATCTCAGTTCACT | 22992 |
rs370368797 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67212773 | TGCTTTCTGTGAATG[A/C]ATGCGTGGTAAAAAA | 22992 |
rs370369096 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67152815 | TATTTAAGTTATTTA[A/G]CTTTTGTAGAATCAG | 22992 |
rs370372314 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67125641 | GCTGGGCACTGGGGG[G/T]GGTGGTGCGTGCCTG | 22992 |
rs370377504 | in-del | -/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67178823 | TGGTTTCTATCTTTT[-/T]GGCTGTTGTGAATAA | 22992 |
rs370405759 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67233400 | GTCTCATGCCTGTAA[C/T]CCCAGCACTTTGGGA | 22992 |
rs370448526 | snp | A/G | 9.1894e-05 | 0.0067778 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | KDM2A | GRCh38.p7 | 11:67217829 | TCTGGGTGACCGGGT[A/G]TCAGATTGTCAGCGC | 22992 |
rs370484414 | snp | G/T | 0.000619947 | 0.0175951 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67250259 | GTCATCCCCTGGGGC[G/T]GGCCCCAGCGACCAC | 22992 |
rs370487904 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67141742 | TAGTCACCCTACTTA[-/A]CGATTGAGCTTCAGA | 22992 |
rs370516474 | in-del | -/AG | | | intron-variant | KDM2A | GRCh38.p7 | 11:67197197 | TTTTTTTTTTGAGAC[-/AG]GGTATTGCTTTGTCA | 22992 |
rs370546947 | in-del | -/TT/TTT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67247422 | AACAGCATTACAATC[-/TT/TTT]TTTTTTTTTTTTTTT | 22992 |
rs370550288 | snp | C/G | 1.65619e-05 | 0.00287762 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67253535 | CCCCCTTCTCAGGAC[C/G]CTTGATCTTCGGTGG | 22992 |
rs370553486 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | KDM2A | GRCh38.p7 | 11:67204599 | TGGGTTCATGCCATT[C/T]TCCTGCCTCAGTCTC | 22992 |
rs370553998 | in-del | -/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67121231 | TATATCATTATTCTT[-/T]AGTGTTGCAATCTGG | 22992 |
rs370557368 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67177160 | AATCCCAGCTACTCG[A/G]GAGGCTGAGGCGAGA | 22992 |
rs370584337 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67188298 | CCATCCTGGCTAACA[C/T]GGTGAAACCCCGTCT | 22992 |
rs370647147 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67138131 | GACCACCGTCACATA[C/T]ACAGTTGTTGAGTGA | 22992 |
rs370664537 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67187839 | TGGGCCTTCCAAGGT[G/T]CTGGGGATTATAGGC | 22992 |
rs370667174 | snp | C/T | 2.86168e-05 | 0.00378254 | intron-variant | KDM2A | GRCh38.p7 | 11:67181442 | GTTGCAAAATGGCCT[C/T]GTTACACCCAGGGCA | 22992 |
rs370676099 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67248091 | CCCTAAACCCAAGCT[A/G]TCAGAACCTGTGCCG | 22992 |
rs370779255 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67203935 | CCTCCTAAGTAGCTG[G/T]GACTATGGCCGCGTA | 22992 |
rs370785716 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67234668 | GAGACCAGCCTGGGC[A/T]ACGTGGCGAAACCTC | 22992 |
rs370799587 | snp | C/T | 0.000165986 | 0.00910854 | intron-variant | KDM2A | GRCh38.p7 | 11:67243002 | TTCTTTTCCCTCCTA[C/T]CCTTAGATTTTGCTG | 22992 |
rs370826179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67145682 | TCTTTCCATTATACC[A/G]TATTCTCCCTTTCTC | 22992 |
rs370871497 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67147497 | CAGTGAGCCGAGATC[C/G]CGCCACTGCACTCCA | 22992 |
rs370925682 | in-del | -/CTA | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67202582 | TTGAGACCATCCTGG[-/CTA]ACATGGTGAAACCCC | 22992 |
rs370926759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67146771 | TGCCTCAGACTCCCA[A/G]AGTGCTGGTGCATGA | 22992 |
rs370928737 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67119804 | GGGGAGGCGGGGGCG[C/T]CCCGGGCTCGGCGCC | 22992 |
rs370932518 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67128529 | TGGTCTCATTGTTGC[A/G]GCCTCCCTCCTAATA | 22992 |
rs370937456 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67172580 | TTTTTTGTTGCTAGT[A/G]TATAGAAATAGAACT | 22992 |
rs370944567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67155638 | ATTTATTTTTTGAAA[C/T]GGAGTTTTGTTGTTG | 22992 |
rs370944991 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67161143 | AAGTTGGGAGGATTG[C/T]TTGAGGCTAGGAGTT | 22992 |
rs370950413 | in-del | -/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67143280 | CAAGGTGTTGGGATT[-/C]ACAGCCGTGAGCCAC | 22992 |
rs370956569 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67220188 | AGCTAATTTTTTTGT[A/G]TTTTTTGGAGATGGG | 22992 |
rs370959274 | snp | C/T | | | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67239350 | ATTTCTAGTACTGTA[C/T]TGTGGGGGTGGAGTC | 22992 |
rs370962111 | snp | C/T | 0.000161987 | 0.00899818 | intron-variant | KDM2A | GRCh38.p7 | 11:67253429 | AACAGTGTATTATTA[C/T]ATGTCTCATTCCATC | 22992 |
rs370974596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67221172 | ATTGGTAAGGGCTGA[A/G]TCATATATGAAAGTA | 22992 |
rs371032458 | snp | C/T | 0.000671723 | 0.0183142 | intron-variant | KDM2A | GRCh38.p7 | 11:67181307 | TCTTTCTAATATTTT[C/T]CTATGGTGACAGATT | 22992 |
rs371038502 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67214619 | GTTGGGGATTACAGG[C/T]GTGAGCCACTGATCC | 22992 |
rs371041310 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67167250 | AGATGCCTTATCCTC[A/G]TCTTGAATTGATAGC | 22992 |
rs371101361 | in-del | -/TTA | 0.0146672 | 0.084371 | intron-variant | KDM2A | GRCh38.p7 | 11:67209432 | TTCTAGAATTTTATT[-/TTA]TTATTATTATTATTA | 22992 |
rs371104183 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67234969 | TGCTAACATGGTGAA[A/C]CCCCGTCTCTAGAAA | 22992 |
rs371106512 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | KDM2A | GRCh38.p7 | 11:67140350 | CATCCTGGGTGACAG[A/C]GTGAGATCTTGTCTC | 22992 |
rs371113782 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67123693 | ACTGTTTTTTTTTTT[-/T]GAGACGGAGTTTCAC | 22992 |
rs371129864 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255514 | GCGCGTCTCTCCTCC[A/G]TCACACTCTCCCGGC | 22992 |
rs371147111 | snp | C/T | 5.04486e-05 | 0.00502213 | intron-variant | KDM2A | GRCh38.p7 | 11:67254871 | TGTCCACTTTCCCGA[C/T]AGGTTGCAATAAATT | 22992 |
rs371150273 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67232765 | CAGGTTGGAGTGCAA[C/T]GGCAAGATCTCGGCT | 22992 |
rs371160613 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67176391 | TACTTAGTTTTAAAT[G/T]CTAGATTTGATGTTC | 22992 |
rs371166964 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67140375 | TGTCTCAAAAAAAAA[-/A]TATCATGGTTTTATA | 22992 |
rs371169500 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67159461 | TAGAAGATTAGATTC[A/T]TCTTAAACATTTTGG | 22992 |
rs371225404 | snp | C/T | 0.000855583 | 0.0206654 | intron-variant | KDM2A | GRCh38.p7 | 11:67243136 | GCTGCTTAAGCCTTT[C/T]GTTAGTTGATCATTA | 22992 |
rs371236913 | snp | C/T | 1.65762e-05 | 0.00287886 | missense, intron-variant | KDM2A | GRCh38.p7 | 11:67250413 | GAGAAAGCCAAGATC[C/T]GGGGATCGTACCTCA | 22992 |
rs371237562 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67153067 | TCAGCTCACTGCAAC[A/G]TCTGCCTCCTGGGTT | 22992 |
rs371257221 | snp | C/T | 0.000161987 | 0.00899818 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67252799 | GCCAGTCAGCCTTGA[C/T]CTCAGTTGGACCAAC | 22992 |
rs371282730 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67222840 | ATTCAGTAACATAAA[A/G]TGAGTACCTTATCCC | 22992 |
rs371288013 | snp | A/C/T | 0.000182435 | 0.0095493 | synonymous-codon, missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67231772 | TCTTCTGACTGTAGC[A/C/T]GGGGCTCCCACAATG | 22992 |
rs371297166 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67161277 | GACAGCATGATCATG[G/T]TAAACTGTGACTTTT | 22992 |
rs371331006 | in-del | -/AACT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67153845 | ACACCAAAAACAACC[-/AACT]GTGTATATCTTGCAC | 22992 |
rs371354281 | snp | A/G | 1.65614e-05 | 0.00287757 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67246081 | CTCATGGAATGCTGT[A/G]TCTGCAATGAGATTG | 22992 |
rs371357116 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67166659 | GAAGCAAGGAGTTCT[A/G]GGCTGTAATGCAGTA | 22992 |
rs371369134 | snp | C/T | 0.000221369 | 0.0105183 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67250168 | GCGATGAGCCTCTCA[C/T]GCCCCCGCCTCATTC | 22992 |
rs371371062 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67154516 | CAGCTCACTGCAGCC[C/T]CTGCCTCCTGGGTTC | 22992 |
rs371374228 | snp | A/G | 3.50275e-05 | 0.0041848 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67250136 | GCAAGCCAAAGTCCT[A/G]CGGCCCCTGCGGAGC | 22992 |
rs371374834 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67125984 | GGCACAGTGTCTCAC[A/G]CCTGTAATCCCAGCA | 22992 |
rs371377962 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67215674 | TAGTCAATACGGTAG[-/A]AAAAAAAAAAAACCT | 22992 |
rs371382664 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67126076 | ACATGGAGAAACCCC[A/G]TCTTTACTGAAAATA | 22992 |
rs371395706 | snp | A/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67178134 | AAGTCAGCTGGGTAT[A/G]GTGACTGAAGCCTGT | 22992 |
rs371400814 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | KDM2A | GRCh38.p7 | 11:67201388 | GCTCATGTCTGTAAT[A/C]CCAATGTTTTGATAG | 22992 |
rs371410820 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67229851 | CTCCAGCTTGGGCGA[C/G]AGAGTGAGACTCCGT | 22992 |
rs371429379 | snp | A/G | 4.97599e-05 | 0.00498773 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67253598 | CTTGCTTACTCCACC[A/G]GCTGATAAACCAGGT | 22992 |
rs371455032 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67236104 | AGCAGGGCACAATAG[A/G]ATAGTAGTAGTCAAC | 22992 |
rs371496319 | snp | A/G | 0.000169986 | 0.00921759 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67181342 | TGTAGAGTATATTCA[A/G]CGGGGTGGCTTGAGA | 22992 |
rs371528444 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | KDM2A | GRCh38.p7 | 11:67229423 | TCAGTATACATTTTT[A/G]GACTCTTATATGTCT | 22992 |
rs371544278 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67141777 | ATTCCTTCTAACTGT[A/G]TGTTCATGCCCATTA | 22992 |
rs371546397 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67169058 | CTGCCGGGGTTCAAG[C/G]GATTCTCTTGCCTCA | 22992 |
rs371558822 | snp | A/T | 0.000265041 | 0.0115087 | intron-variant | KDM2A | GRCh38.p7 | 11:67215980 | TGATAGGGGTTGGAA[A/T]CTGAAGTTGGTTGTA | 22992 |
rs371650924 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67135008 | AGATCAACTTATTTC[A/G]GTAACATAAGCATTC | 22992 |
rs371682532 | in-del | -/GTTCTACTTA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67254095 | GGGCAGTTCTACTTA[-/GTTCTACTTA]ACCCCTTCAAGGGGG | 22992 |
rs371739647 | snp | A/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185399 | CACTTTGGGAGGCCA[A/G]GGCGGGTGGATCACT | 22992 |
rs371767777 | in-del | -/G | 0.0193772 | 0.0965046 | intron-variant | KDM2A | GRCh38.p7 | 11:67147689 | TTAGAGATTCTTTTT[-/G]TTTTTTGAGATGGAG | 22992 |
rs371776268 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67191187 | AGCTGGGATTATGCC[C/T]GGCTAATTTTTTGTA | 22992 |
rs371779767 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67150607 | ATCAAGAGGAAAGGG[C/T]TGGCCATAGTTACTA | 22992 |
rs371783712 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67127186 | CTTTGTAGCCTCAAC[C/T]GCCTGGCTCAAGTGG | 22992 |
rs371852790 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67155870 | ATCCGCCTGCCTCGG[C/T]CTCCCAAAGTGCTGG | 22992 |
rs371890552 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67218682 | TGATCTTGGCTCACT[A/G]CAACCTCCACCTCCC | 22992 |
rs371900856 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67184310 | ATCAGCCTGGCCAAC[A/G]TGGGGAAACTCCATC | 22992 |
rs371905693 | snp | C/T | | | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67254390 | CGGGTCTTCCACTCG[C/T]TACTCTCTCACAGAG | 22992 |
rs371911656 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant | KDM2A | GRCh38.p7 | 11:67181963 | TGAATTAAATCTCTG[A/G]CTGAGATTTAAGGCC | 22992 |
rs371971917 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | KDM2A | GRCh38.p7 | 11:67142108 | CAGTGGCACGATCTC[C/T]GCTCACTGCAACCTC | 22992 |
rs371980237 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67169502 | CTCGTGCCTCAGCCT[C/T]CTGAGTAGCTGGGAT | 22992 |
rs371994261 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | KDM2A | GRCh38.p7 | 11:67147490 | GAGCTTGCAGTGAGC[C/T]GAGATCGCGCCACTG | 22992 |
rs372060854 | in-del | -/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67157332 | CAAAAAAAAAAAAAA[-/C]AAAAAACACCACACA | 22992 |
rs372097089 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67192466 | TTTTTTTTTTTGAGA[C/T]GGAGCATCTCTCTTG | 22992 |
rs372108346 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67252354 | TATACACTTCAGCAG[A/G]AACCATGCCATTTTA | 22992 |
rs372109391 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67122317 | CTTTTTGAGAAGAGA[C/G]TTCTTTATTATTTAT | 22992 |
rs372121894 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67211073 | AAACAAACAAACAAA[C/G]AAAAACATAGCTACA | 22992 |
rs372127075 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KDM2A | GRCh38.p7 | 11:67175859 | TTATTCTAGTAGCAT[C/T]GCTCTTGCTTTATAA | 22992 |
rs372135821 | multinucleotide-polymorphism | AA/GC | | | intron-variant | KDM2A | GRCh38.p7 | 11:67254458 | TCAGCGGTGCCCCCT[AA/GC]CTCCAGCCCTCCCTG | 22992 |
rs372143811 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67201214 | AAAAAATATATATAT[A/G]TATATGTGTGTGTGT | 22992 |
rs372149127 | snp | A/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67177804 | TTATGTACTATTCCT[A/G]ACAGTATGTGCTACA | 22992 |
rs372158893 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67163022 | GCCATGATTTCTTTT[C/T]CTTAAAGTTAGGAAT | 22992 |
rs372163100 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67222875 | ATGAAGAGTTTTCTA[C/T]GTAAAGAGAAGAAAA | 22992 |
rs372178788 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | KDM2A | GRCh38.p7 | 11:67223547 | AGCTGGGACCACAGA[C/T]GCACACCACCACACC | 22992 |
rs372207033 | snp | G/T | 0.000165986 | 0.00910855 | intron-variant | KDM2A | GRCh38.p7 | 11:67245470 | GGCAGTGAGTGATCT[G/T]CTGGGTAAAGAATTT | 22992 |
rs372248975 | in-del | -/CTC | 0.00438332 | 0.0466095 | intron-variant | KDM2A | GRCh38.p7 | 11:67163073 | TTAGTTACTTCTCTT[-/CTC]CTTTAGTTTGTTTTC | 22992 |
rs372286746 | snp | A/G | 8.28411e-05 | 0.00643535 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67245357 | AAATGCAAAGCCTGT[A/G]TGCAAGGAGAGTGTG | 22992 |
rs372326422 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KDM2A | GRCh38.p7 | 11:67156310 | AAAGTATTGGCTGGG[C/T]GCAGTGGCTCACGCC | 22992 |
rs372349227 | multinucleotide-polymorphism | CA/TG | | | intron-variant | KDM2A | GRCh38.p7 | 11:67204531 | AGAGTCTCACTGTGT[CA/TG]CCCAGGCTGGAGTGC | 22992 |
rs372359751 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67234680 | GGCAACGTGGCGAAA[A/C]CTCACCTCCACAAAA | 22992 |
rs372377083 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67164787 | TATTTTTAGTGGAGG[G/T]GGGGTTTCACTATGT | 22992 |
rs372380873 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67122454 | GCCTCAGCCTTGCAA[G/T]TAGCTGGGACTGTAG | 22992 |
rs372416402 | snp | A/G | 1.90123e-05 | 0.00308315 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67231647 | GCTTGAGCAGCAGGC[A/G]TTCTGTCCTCACTAG | 22992 |
rs372428295 | snp | G/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67179240 | CTAAATATTGATGGT[G/T]TGCTATTTGGAATGC | 22992 |
rs372455798 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67127385 | CTTGGCTTCCCAAAG[C/T]GCTGGGAGTACAGGT | 22992 |
rs372482729 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67149032 | GAAATATCCCAAAAC[A/G]TTCATTTTTGCTTCC | 22992 |
rs372490525 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67208497 | ACCTTGGGGCCAGGC[A/G]CAGTGGCTCATGCTT | 22992 |
rs372542104 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67165080 | TGGTGGTAGTGGGAC[A/G]GGTAGGAGTATATGT | 22992 |
rs372604728 | in-del | -/TCCT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67192198 | TCAATCCCTTTTCCT[-/TCCT]CCTCTCTCCAGAGAT | 22992 |
rs372647507 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67124293 | ACAGGTGTGAGCCAC[A/C]GTGCCCGGCTTCACT | 22992 |
rs372756373 | snp | C/T | 1.65776e-05 | 0.00287898 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67181864 | GCCGGATCCAGACTT[C/T]ACTGTGAATGATGTC | 22992 |
rs372798866 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67240893 | CACATACCCCAGTAA[C/T]TGAGTCTTGTATGTG | 22992 |
rs372800759 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67170476 | GGAGTGCAGTGGCGC[A/G]ATCTCAGCTCACTGC | 22992 |
rs372847571 | snp | C/T | 0.00016575 | 0.00910205 | intron-variant | KDM2A | GRCh38.p7 | 11:67228198 | GAGCTTTGAAGACAC[C/T]GCTTAGGTCTGAGGG | 22992 |
rs372880436 | in-del | -/AAA | 0.00199481 | 0.0315187 | upstream-variant-2KB, cds-indel | KDM2A, LOC107984341 | GRCh38.p7 | 11:67117662 | AACCAAGGCAGGGAG[-/AAA]AAGATTTGTGTGACA | 22992 |
rs372909104 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67151549 | GAGACCGGGGTTTCA[A/C]CATGTTGGCCAGGCT | 22992 |
rs372921095 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67210159 | GATTGCTTGAGCTCA[A/G]GAGTTTGATACCAGC | 22992 |
rs372925935 | snp | A/C/T | 5.4272e-05 | 0.00520898 | missense, intron-variant | KDM2A | GRCh38.p7 | 11:67250737 | TGGATGTCTGTCTTC[A/C/T]GCTACCTCAGCCGCA | 22992 |
rs372929497 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67194545 | ATCATGTAAATACTG[C/T]GAGAAGGTAAAAAAC | 22992 |
rs372987587 | snp | A/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185054 | TGGATCTAATAGACA[A/G]AGATTTTTAAATAGC | 22992 |
rs372991424 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67219819 | GCCTCCCAAAGTGCT[A/G]GGATTACAGGTGTGA | 22992 |
rs372996379 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67244302 | TAAATGCAAATGCTA[A/G]GAAATGTGTTCCACA | 22992 |
rs373008302 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67196087 | TTAAGCTGAGTCACA[C/T]GAACATAATTGTCGG | 22992 |
rs373063676 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67233345 | CCAACATGGTGAAAC[C/G]CCATCTCTACTAAAA | 22992 |
rs373087204 | snp | C/T | 0.000163987 | 0.00905353 | intron-variant | KDM2A | GRCh38.p7 | 11:67215841 | ACACTAATGCTGCTG[C/T]TTTTTTTGGGTCAGG | 22992 |
rs373104241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67212492 | GTGATGGGGAAATAA[A/G]TTCATGGAAGGCTAT | 22992 |
rs373125477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67143909 | AGTGCTGGGTTTACA[A/G]GCATGAGCCACTGTG | 22992 |
rs373144982 | snp | A/G/T | 3.31248e-05 | 0.00406958 | synonymous-codon, missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67231807 | AGTGTGGGATCCCCA[A/G/T]TGTGCTCCCCGAAAG | 22992 |
rs373146142 | snp | A/G | 0.000157987 | 0.00888643 | synonymous-codon, intron-variant | KDM2A | GRCh38.p7 | 11:67250778 | TGAATGTATGCGAGT[A/G]TGCAAGACGTGGTAT | 22992 |
rs373160417 | snp | C/T | 0.000100339 | 0.00708235 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67252700 | CTATCACAGGTGCTG[C/T]GACAAGAGACTTTGG | 22992 |
rs373162346 | snp | C/T | 0.00998976 | 0.0699649 | intron-variant | KDM2A | GRCh38.p7 | 11:67170985 | CTGGGCAAGTTACTT[C/T]TTTCATTTTCCTTGC | 22992 |
rs373173916 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant | KDM2A | GRCh38.p7 | 11:67181258 | CTTAGGATCCTTTTT[A/G]TGGTCCTTTTATCGT | 22992 |
rs373178331 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67201967 | CTCTAAAAAAAATAA[G/T]TAAAATGAAAAAGAG | 22992 |
rs373226124 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67137872 | GTGCGATCTCGGCTC[A/G]CTGCAACCTCTGCCT | 22992 |
rs373230533 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67138479 | CATTACCTGGGAACT[A/T]GTTAGAAAGGGAATT | 22992 |
rs373234200 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67152222 | GGAGGCTGAGGTGGG[A/G]GGATCACTTGAGCCC | 22992 |
rs373238987 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67179891 | CCCAGTGGCTCATTG[A/G]AACTTCATTATATTC | 22992 |
rs373248818 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67213920 | CCCAAGCTGGAGTGC[A/G]GTGGTGATCGTAGCT | 22992 |
rs373253980 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67237091 | TAAACTTTCCTGTTA[C/T]AGGATATAAATTTAT | 22992 |
rs373287668 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67233313 | CACCTGAGGTCAGGA[A/G]TTCGAGACCAGCCTG | 22992 |
rs373354915 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67225000 | GTATGCACCACCACG[A/C]TAATTTTTGTATTTC | 22992 |
rs373397338 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67132440 | AGGCACGTGCCACCA[C/T]GCCCGGCTAATTTTT | 22992 |
rs373403280 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67203033 | AGAAAAACGGTTTAC[A/G]CTTCAGCGAAAGAAA | 22992 |
rs373406719 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67140231 | ATTAGCTGGCTGTCA[C/T]GGCGTGTACCTCTAG | 22992 |
rs373418364 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67158985 | TTTTCATTCCTTTGA[C/T]AGTGTCTTTCACAGA | 22992 |
rs373422699 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67186876 | AATTCAAGACCAGCC[C/T]GGGCAACATAGCAAA | 22992 |
rs373425023 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67166345 | ACATGCCATCATGCC[C/T]GGCTAATTTTCACAT | 22992 |
rs373428090 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67203399 | TAAGTAGTCTGAAAA[C/T]ACAAAATAGTCTAGT | 22992 |
rs373431686 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67247941 | ACCACAACCCTATAA[A/G]GTGGGTTTTGTTGTA | 22992 |
rs373436005 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67136153 | TTGATTGAATGTGTA[C/T]TGTGTGCTTGGTACT | 22992 |
rs373445768 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67226574 | AAAAATACAAAAAAT[C/T]AGCCGGGCGTGGTGG | 22992 |
rs373485114 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67220929 | TTATATAGTTCATGA[C/T]CATGATTAGGTGTTC | 22992 |
rs373506603 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67203863 | CGGAGTGCAGTGGTG[C/T]GATCTTGGCTCACTG | 22992 |
rs373536076 | snp | G/T | 7.96258e-05 | 0.00630924 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67181360 | GGGTGGCTTGAGAGA[G/T]CCTCTGATTTTCAAG | 22992 |
rs373584021 | snp | A/G | 1.6569e-05 | 0.00287824 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67231787 | CGGGGCTCCCACAAT[A/G]GACAAGTGTGGGATC | 22992 |
rs373596411 | snp | A/C/G | 6.67295e-05 | 0.00577591 | synonymous-codon, missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67254896 | TAAATTGACAGACCA[A/C/G]ACCCTGATCTACCTA | 22992 |
rs373611385 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67141566 | CAGCTGCTCGGGAGG[C/G]TAAGGCAGGAGAATG | 22992 |
rs373615464 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67254455 | TAATCAGCGGTGCCC[C/T]CTGCCTCCAGCCCTC | 22992 |
rs373619308 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67223380 | CATATTTTCTTCCTT[C/T]TTTCTTTCTTATTTA | 22992 |
rs373632215 | snp | C/G | 1.6727e-05 | 0.00289193 | intron-variant | KDM2A | GRCh38.p7 | 11:67243131 | TTTAGGCTGCTTAAG[C/G]CTTTTGTTAGTTGAT | 22992 |
rs373637778 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67146104 | TCAAGCGATTCTCCT[C/G]TCTCAGCCTCCTGAG | 22992 |
rs373669747 | snp | A/G | 4.9703e-05 | 0.00498488 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67253579 | AGGACCCTCAAATTC[A/G]GGACTTGCTTACTCC | 22992 |
rs373683863 | snp | A/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67120901 | CAGCTCTCTGGAGAT[A/G]AAAGTCCTGGGCTTT | 22992 |
rs373733607 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67191808 | TTTTACTGCCTCTAT[G/T]CAATGTAGCACTGGA | 22992 |
rs373804110 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67147036 | TTGCTTAGTCAGATA[C/T]AAATAGCCAGAAAAC | 22992 |
rs373821288 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206932 | GGAATAAATGAAAAG[A/G]GGACTTTGTTCTTCA | 22992 |
rs373856976 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67125187 | TTCTTTTTTTTTTTT[C/T]TTTTTTTTTTATTTG | 22992 |
rs373876213 | snp | C/G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67197288 | AAGCGATCCTCCCAC[C/G/T]TCAGCTTCCTGAGTA | 22992 |
rs373901181 | snp | G/T | 1.83859e-05 | 0.00303193 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67254998 | CTTCATCTCAGACTT[G/T]TCCATCAACAGCCTC | 22992 |
rs373916972 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67169233 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGCACC | 22992 |
rs373922045 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67175813 | AAAATGCAAGTGAGT[A/G]CTTTCTAAAAGTGAT | 22992 |
rs373966938 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67229954 | GGCCGAGGAGGGCCA[A/G]TCACGAGGTCAGGAG | 22992 |
rs373973391 | snp | C/T | 0.000482189 | 0.0155197 | intron-variant | KDM2A | GRCh38.p7 | 11:67207711 | TAATCATTTTCTTCA[C/T]ATTGTCATTGTCACC | 22992 |
rs373978735 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67186604 | CATGGGTAATTGTAA[G/T]AGCTAGTATTATCTT | 22992 |
rs373990679 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67217110 | AGCTGGGTGTGGTGG[C/T]GCACGCCTGTAGTCC | 22992 |
rs373994623 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67245879 | ATGCTTCCAGGTGTT[C/T]AGTAGAGAATTATAG | 22992 |
rs374006715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67197428 | GCAGTCAGCCCGCCT[C/T]GGCCCCACCAAAGTG | 22992 |
rs374069793 | snp | C/T | 3.44548e-05 | 0.00415045 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67252841 | GCAACTGACATGGCT[C/T]GTCAATAGGCTGCCA | 22992 |
rs374121079 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67180963 | CACCACACCTGGCCC[-/T]TTTTTTTTTTTTTTT | 22992 |
rs374147942 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67132972 | AAGACACATTGGCAG[C/T]GAAGGACTGACTAAA | 22992 |
rs374154149 | in-del | -/CTTTTTT | 0.0115144 | 0.0749975 | intron-variant | KDM2A | GRCh38.p7 | 11:67139244 | CTTTTTTTTTTTTTC[-/CTTTTTT]CTTTTTTCTTTTGAG | 22992 |
rs374173214 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67175935 | AAAATAAGGTGAGGG[A/G]GAGAACTGGATGATG | 22992 |
rs374191846 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255647 | TCCTTTCCTCTCCCT[C/T]GAGCTTGGTTCTGCC | 22992 |
rs374194059 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67214790 | CTTAGTTTTATAGAT[A/G]AGTTTGAGGGCCTTA | 22992 |
rs374198422 | in-del | -/GTTTTGTT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67198778 | GTTTTGTTTTGTTTT[-/GTTTTGTT]TTGTTTTGTTTTTGA | 22992 |
rs374218955 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67157090 | AGGCCGAGAAGGGCC[A/G/T]ATCACGAGGTCAGGA | 22992 |
rs374223133 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67190635 | ACATGGTTGCATGTT[A/C]CTGTAATCCCAGCTA | 22992 |
rs374232204 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67214224 | TTTTTTTTTTTTTTG[A/T]GACGGAGTCTTGCTC | 22992 |
rs374330308 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67233402 | CTCATGCCTGTAATC[C/T]CAGCACTTTGGGAGG | 22992 |
rs374354689 | snp | A/G | 0.000204198 | 0.0101023 | intron-variant | KDM2A | GRCh38.p7 | 11:67181443 | TTGCAAAATGGCCTC[A/G]TTACACCCAGGGCAA | 22992 |
rs374383946 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67140677 | AGAGTTGCTTGAACC[C/T]GTGAGGCGGAGGTTG | 22992 |
rs374396229 | snp | A/C | | | intron-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67120062 | CCGGTGAGTTTCCCC[A/C]TCCCCCCCCTCATTT | 22992 |
rs374399229 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67145730 | AATGATACCATACTC[A/G]GCTACTTTCTCTTTT | 22992 |
rs374404039 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67198626 | GAGTCAGGAGAATGG[C/T]GTGAACCCGGAAGGC | 22992 |
rs374414971 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255108 | CCCCTGACTCCCCAC[C/T]GAGGAGAGCCTCTCC | 22992 |
rs374416562 | snp | C/T | 1.65608e-05 | 0.00287752 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67228074 | CATTCTACTATGAGA[C/T]GTGTTGGTATGTGTT | 22992 |
rs374423227 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67202935 | AGGAGTTTGTGGCTG[G/T]GGTGAGCTGTGATTG | 22992 |
rs374462565 | in-del | -/TC | | | intron-variant | KDM2A | GRCh38.p7 | 11:67169734 | CTCTCTCTCTCTCCT[-/TC]TCTCTCTCTCTCTCT | 22992 |
rs374487868 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67231449 | GATAGACCATTTTTT[A/T]AAATGTGGTAATTTT | 22992 |
rs374503777 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67237455 | CTTTATTATTATTAT[C/T]ATCATTATTATTATT | 22992 |
rs374533543 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67153393 | AACCCAGTTTTTAGA[C/T]ACCCTGGCTCCCAAA | 22992 |
rs374579802 | snp | C/G/T | | | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67119992 | GATTTAATTATTCCT[C/G/T]TCAGCTTTGGAATCT | 22992 |
rs374586437 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67173282 | CATGCGCCACCATGC[A/G]TGGCTAATTTCGTAT | 22992 |
rs374627078 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67251330 | CCCCCAAACCTGGAT[C/T]AGAATTCCCTCTTCC | 22992 |
rs374629762 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67147248 | GTCAGGTTAAAAGAT[A/G]TGACTTCCACTGGGC | 22992 |
rs374642382 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67183375 | GACATTCTTACAGAT[G/T]GTGGTCCACAGATGA | 22992 |
rs374654359 | snp | C/T | | | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67238924 | AACCAGAGTGTGCAC[C/T]CTCCTTTCCTCCTGT | 22992 |
rs374668250 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67201508 | CGGTGCGGTGGCTCA[C/T]GCCTGTAATCCTAGC | 22992 |
rs374774970 | snp | A/G | 1.65795e-05 | 0.00287914 | missense, intron-variant | KDM2A | GRCh38.p7 | 11:67250464 | ACCAAAGAGCTCCAC[A/G]GGACATCCATTGTGC | 22992 |
rs374798610 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67227789 | TTGGTCAGGCTGGTC[A/G]CGAACTCCTGACCTC | 22992 |
rs374824676 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67184158 | TTCTCCTAATTGTTG[C/G]AGGCCTCTTCCCCTC | 22992 |
rs374837135 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67161509 | CATTTTATATTACTA[C/T]GTATTACTATTATAT | 22992 |
rs374843450 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67241496 | TAGGTTAAGAATGAA[A/G]ATACATAAAAGTCCT | 22992 |
rs374844992 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67163109 | CTTCTGCCCTAGTCA[A/G]ACTGATATCCAGAAT | 22992 |
rs374852787 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67123564 | AACTCCTTTCCCAGG[C/T]AGTTATTGCTATATG | 22992 |
rs374876245 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67140332 | GATTACGCCACTGCA[A/C]TCCATCCTGGGTGAC | 22992 |
rs374915907 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67157283 | GCGCCACTGCACTCC[A/G]TCCAGCCTGGGCGAC | 22992 |
rs374924066 | snp | A/G | 0.00050196 | 0.0158344 | intron-variant | KDM2A | GRCh38.p7 | 11:67250060 | AAAGGAAGCACTGAT[A/G]TTGCTTTTCTGGGCC | 22992 |
rs374938028 | snp | A/T | 0.000333228 | 0.0129036 | intron-variant | KDM2A | GRCh38.p7 | 11:67245942 | ACTGAAATGATAAAG[A/T]TCTGAGTCAGTTCTC | 22992 |
rs374956650 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | KDM2A | GRCh38.p7 | 11:67209746 | ACTGTACCCGGCCAA[C/T]TTCCAGAATTTTAAT | 22992 |
rs375024360 | snp | C/G/T | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67127300 | CAGGCTATCCCTGTT[C/G/T]GGGCTGCTCAGGCTG | 22992 |
rs375052017 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67208164 | AAAGATATATTGATA[C/T]TGTATTTTGATAAGA | 22992 |
rs375061402 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67217322 | TGTTTGCTTCAGATC[C/G]CTTTAAGCCCTGTTG | 22992 |
rs375063005 | snp | A/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185551 | AGGAGAATTTATTGA[A/G]CCCGGGAGGTGGAGG | 22992 |
rs375108679 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67137837 | GGTCTCAGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 22992 |
rs375113795 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67252181 | AAGAGCCTCTTTTGA[C/T]CTGATACAGTAATGG | 22992 |
rs375180739 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67157869 | ACTCCAGGTGGGGCT[C/T]ACTTGAGCTCAGGAA | 22992 |
rs375184290 | snp | A/C | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185189 | GAAATTCTGGAGCTG[A/C]AAAGTACAATAATTA | 22992 |
rs375190298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67244547 | AACAGCTCTGCAAAA[A/G]GAAAGGGAAGCAGCT | 22992 |
rs375196411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67224186 | GAACACTACCCGATA[C/T]AGAGTTTGTAAACGG | 22992 |
rs375204198 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255979 | CCAAGCTGGAGGCGG[C/T]AGAGGACTGGGCCAA | 22992 |
rs375225409 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | KDM2A | GRCh38.p7 | 11:67219106 | TGAGCAACCATAAGA[A/G]GTATTATTTATCCTG | 22992 |
rs375250832 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67201049 | TAGAAAAAAAATTAG[A/C]CGGGCGTGGTGGCGG | 22992 |
rs375285238 | snp | A/G | 4.97327e-05 | 0.00498637 | intron-variant | KDM2A | GRCh38.p7 | 11:67246129 | CAGGTGAGGAGAGCT[A/G]TGAGGGGTTCCTGAA | 22992 |
rs375370936 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67162224 | GGTGGCATATTTTTC[A/G]CCAGAGTTTCTCTTC | 22992 |
rs375386312 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67192475 | TTGAGATGGAGCATC[G/T]CTCTTGGTGCCCTGA | 22992 |
rs375389895 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67201216 | AAAATATATATATAT[A/G]TATGTGTGTGTGTGT | 22992 |
rs375446169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67133262 | GCGCCACCACACTGC[A/G]CTAATTTTGTGTTTT | 22992 |
rs375456699 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67137293 | GGAAGGCAGAAGTTC[A/G]GCAGAGTAGTAATGC | 22992 |
rs375463217 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67190684 | GAGAATCGCTTGAAC[C/T]GAGGAGGCGGAGGTT | 22992 |
rs375467196 | in-del | -/TATATATAT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67141684 | AAAAAAAAAAAAAAA[-/TATATATAT]ATATATATATATATA | 22992 |
rs375486785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67233741 | TGGTACAATGGTATA[C/T]CAAAGGAAAAAGTAG | 22992 |
rs375495319 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67159991 | GCTGAACTATACACA[A/G]ATTCAGCTAAAATGG | 22992 |
rs375503206 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67122877 | AGACGGGGTTTCACT[C/G]TGTTAGCCAGGATGG | 22992 |
rs375517446 | snp | C/T | 8.52939e-05 | 0.00652991 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67248304 | AGAGGGGTTGCTTAA[C/T]GAAGAATTGCCAAAT | 22992 |
rs375518283 | snp | C/T | 7.26903e-05 | 0.00602825 | missense, intron-variant | KDM2A | GRCh38.p7 | 11:67250749 | TTCCGCTACCTCAGC[C/T]GCAGAGAACTTTGTG | 22992 |
rs375519813 | snp | A/C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67184097 | AGTGAGACCCTGTCT[A/C/T]AAAAAAAAAAAAAAA | 22992 |
rs375528829 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67227127 | CTCTTTTGGGAAGAA[C/T]GGAAAGAAAATAAAG | 22992 |
rs375529157 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67195974 | TTCTATCAACTCAAG[A/G]TGTTGTGATTTCTTC | 22992 |
rs375532284 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67122045 | CTATTGGAGTTTTAA[C/G]AATTCAATTTTTGTT | 22992 |
rs375533015 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67126139 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 22992 |
rs375549164 | in-del | A/TT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67145887 | CTTTGGGAATTTTTT[A/TT]TTTTTAATTCCTGCT | 22992 |
rs375592749 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67182947 | TGTACTAAAGCTCCA[C/G]TGCCATTCCTTTGCT | 22992 |
rs375601261 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | KDM2A | GRCh38.p7 | 11:67214200 | CATGCGCCACCATGC[A/G]CAGCTAATTTTTTTT | 22992 |
rs375645780 | snp | A/G/T | 0.000170844 | 0.00924105 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67231629 | GAAGTCTTCCAAGT[A/G/T] | 22992 |
rs375647144 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67193801 | AGGAGCGGGAGGTTG[C/T]GGTAAGCTGAGACCA | 22992 |
rs375651535 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67133842 | GGGTTTACAGCCCTG[C/T]GCCACCACACCCAGG | 22992 |
rs375667964 | snp | A/G | | | synonymous-codon, intron-variant | KDM2A | GRCh38.p7 | 11:67240246 | TATTCAAGTAAATCC[A/G]GATTTTCCCAGAGGC | 22992 |
rs375674067 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67141701 | TATATATATATATAT[A/G]TATATAAAATTCATT | 22992 |
rs375732510 | snp | A/G | 0.000165986 | 0.00910855 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67181865 | CCGGATCCAGACTTC[A/G]CTGTGAATGATGTCA | 22992 |
rs375753382 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67156353 | ACTTTGGGAGGCTGA[A/G]GCAGGTGGATCATGA | 22992 |
rs375765414 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67218383 | TACGCTTAGAGCAAA[C/T]ATTTAAATCTGTGTC | 22992 |
rs375774422 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67190136 | AAGTGAGGGCCGAGC[A/G]CGGTGGCTGACACCT | 22992 |
rs375814635 | in-del | -/TC | | | intron-variant | KDM2A | GRCh38.p7 | 11:67179498 | GGCTGGTCTCTAATC[-/TC]GAACTCCCGACCTCA | 22992 |
rs375822345 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KDM2A | GRCh38.p7 | 11:67165145 | TTTTTTTTTGAGACC[A/G]ACTTTCACTCTTGTT | 22992 |
rs375833360 | snp | C/T | 0.00398564 | 0.0444627 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255243 | GCTTATCTGCCTGCT[C/T]CTCTCCCTCCTAAGG | 22992 |
rs375853142 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67212190 | TGGAAGGATGACCTA[A/G]TTTAGAAACTATAGG | 22992 |
rs375861603 | snp | A/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67178324 | GTGGGAGGATCACCT[A/G]AGCCTAGGAGGTTGA | 22992 |
rs375907501 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67170404 | TTTTTTTTTTTCTTT[C/T]TTTCTTTTTTTTTTT | 22992 |
rs375922024 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67156871 | TTCATCCAGCCTGCT[A/G]ACAGGGTGAGACTCT | 22992 |
rs375930125 | snp | C/T | 0.000165986 | 0.00910854 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67245197 | TTTCCAGCTTAAATT[C/T]CCCACTCGGCCAAAG | 22992 |
rs375954845 | snp | C/T | | | intron-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67120069 | GTTTCCCCCTCCCCC[C/T]CCTCATTTGGAAGTT | 22992 |
rs376038424 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67225615 | GTTTCTACTAAAAAT[A/G]CAAAATTAGCCAGGT | 22992 |
rs376048712 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67233391 | CAGTGCGATGTCTCA[C/T]GCCTGTAATCCCAGC | 22992 |
rs376082139 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67243203 | GGCTTTTGGTGCATT[A/G]ATACAAACTGACAGA | 22992 |
rs376094622 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67242735 | GTCTCAAACTCCTGG[C/T]TCAAGTGATCCTCCC | 22992 |
rs376117530 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67160310 | GTTGCAGTTCACCAG[A/G]TGCTGGCCTGCCTTT | 22992 |
rs376156424 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67126618 | GAGGCTCAGACAGGA[A/G]AATTGCTTGAACTCG | 22992 |
rs376158278 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67189268 | AAAACTGGAAAGGTC[A/G]CAAAATTGTGGAATT | 22992 |
rs376205118 | snp | C/T | 3.31318e-05 | 0.00406999 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67231794 | CCCACAATGGACAAG[C/T]GTGGGATCCCCAGTG | 22992 |
rs376237870 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | KDM2A, LOC107984341 | GRCh38.p7 | 11:67118553 | GCCCCTTCCCTGCGC[C/T]CTCTCGCCCTGGGCA | 22992 |
rs376260180 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67182270 | TTCCAGGAAATGCTC[A/G]CCAGTGCTGCATTTG | 22992 |
rs376276572 | snp | A/T | 1.77093e-05 | 0.00297562 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | KDM2A | GRCh38.p7 | 11:67217793 | GAATTGGCTGCTGTC[A/T]GGGAAACAGGGAGAC | 22992 |
rs376360848 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67211169 | TTCATTTATCTAGGT[C/T]TTTTCCAGTATATTT | 22992 |
rs376376051 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KDM2A | GRCh38.p7 | 11:67141388 | TTCATTGTTATTGGC[C/T]GGGCGCGGTGGCTCA | 22992 |
rs376412235 | snp | A/G | 1.7828e-05 | 0.00298558 | intron-variant | KDM2A | GRCh38.p7 | 11:67231981 | GGTTTGATGTGTTAC[A/G]TGACAGCTACTGATC | 22992 |
rs376424971 | in-del | -/AAGG | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67252267 | CTGCGAGTGATTGAC[-/AAGG]GAGGGAACGGAGCAG | 22992 |
rs376428622 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67214324 | ATTCTCCTGCCTCAG[C/T]CTCCCGAGTAGCTGG | 22992 |
rs376429935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67140989 | TAATTTTTCTCCAGA[C/T]CTCTTACCTCATGCT | 22992 |
rs376432946 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67237905 | AGCCTGGGCAACAAA[A/G]CGAGACCCTGTCTGA | 22992 |
rs376438599 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67204349 | TTGAGCAGTCATTCT[C/G]CGTTTTCTCCTCCAC | 22992 |
rs376441434 | in-del | -/GA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67121941 | TAGATCTTGTTGAAA[-/GA]AATTTTAGACATGAT | 22992 |
rs376497826 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67146892 | ATTCCTTAACTGGAA[A/T]ACAAATAGGTTTCAT | 22992 |
rs376510147 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206142 | CTGAGATTTAAACTT[A/C]GGTCTCAGGCAGGTG | 22992 |
rs376533607 | snp | C/T | 5.60099e-05 | 0.00529167 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67248311 | TTGCTTAACGAAGAA[C/T]TGCCAAATTGCTGGG | 22992 |
rs376548434 | snp | A/G | 1.91258e-05 | 0.00309233 | intron-variant | KDM2A | GRCh38.p7 | 11:67215454 | GTGCAGAAGTAAGTG[A/G]TGCGCCCTGCATCTT | 22992 |
rs376554175 | snp | C/T | 9.95388e-05 | 0.00705404 | intron-variant | KDM2A | GRCh38.p7 | 11:67254425 | ATATGGCAGGTATGC[C/T]GCTACAGTTGTTCAT | 22992 |
rs376575583 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67210184 | ACCAGCCTGGGCAAC[A/G]TGGTGAAACCCTGTC | 22992 |
rs376582766 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67165540 | TTGTTGATTAAGAGA[A/C]TGACCTTTGTCTATG | 22992 |
rs376615443 | snp | C/T | 4.98029e-05 | 0.00498988 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67253608 | CCACCGGCTGATAAA[C/T]CAGGTATGCTCTGGA | 22992 |
rs376645095 | snp | C/T | | | upstream-variant-2KB, utr-variant-3-prime | KDM2A, LOC107984341 | GRCh38.p7 | 11:67117374 | CTCCTAAGGATGTTG[C/T]GAAACAAAGCAGAGA | 22992 |
rs376656070 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67231495 | AAGGCCCCTATCATG[C/T]CACCTATTTCTCTTG | 22992 |
rs376683162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67165199 | CGATCTTGGCTCACC[A/G]CATCCTCCACCTTCT | 22992 |
rs376702693 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67194853 | TGTATCTAAGATTCA[A/G]CATTCATGAAGGAGC | 22992 |
rs376714030 | snp | C/T | 1.66407e-05 | 0.00288446 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67231742 | AGTCTGAAGAAAACT[C/T]TGGCTGGGGACTCAT | 22992 |
rs376717337 | snp | A/G | 1.68077e-05 | 0.00289889 | intron-variant | KDM2A | GRCh38.p7 | 11:67180060 | CATGATTTCATCAGT[A/G]TGTTCCTTTCTTTCC | 22992 |
rs376765170 | snp | A/G | 1.77077e-05 | 0.00297549 | intron-variant | KDM2A | GRCh38.p7 | 11:67252672 | AGTTAATGAAGGCGA[A/G]TTCTCTTCCCTTCTA | 22992 |
rs376769126 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | KDM2A | GRCh38.p7 | 11:67204863 | TTTTTATGGTCGACT[A/G]TTTCCTTGTATGGAT | 22992 |
rs376794184 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67197225 | GTCACCCAGGCTGGA[G/T]TGCAGTGGGGCAATC | 22992 |
rs376819117 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67246964 | TGTTTTTGAGACATA[A/G]CCTTGTGTTGTTGCC | 22992 |
rs376855792 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67229408 | GATGACAGTGTAGTT[A/T]CAGTATACATTTTTA | 22992 |
rs376881286 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67194722 | CCATCAGGAAGGAGG[A/T]ACAAGGATAGATCCA | 22992 |
rs376886081 | snp | C/T | | | downstream-variant-500B | KDM2A | GRCh38.p7 | 11:67258434 | GATTACAGGCACTTA[C/T]CATCATGTCCAGCTA | 22992 |
rs376899205 | snp | C/T | 0.000165986 | 0.00910855 | intron-variant | KDM2A | GRCh38.p7 | 11:67215957 | GGGGAAAGGTATGGT[C/T]ATAGTTGTGATAGGG | 22992 |
rs376952115 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67167091 | TCAAAAAAAAATTAA[A/G]AAGTTTAATATTGCG | 22992 |
rs376986561 | snp | A/C | 6.99472e-05 | 0.00591343 | intron-variant | KDM2A | GRCh38.p7 | 11:67252871 | AGGTAAGTGAGCAGC[A/C]CTGCCGCTGTCTTTC | 22992 |
rs376996087 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67214226 | TTTTTTTTTTTTGAG[A/T]CGGAGTCTTGCTCTG | 22992 |
rs377003771 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67233324 | AGGAGTTCGAGACCA[G/T]CCTGGCCAACATGGT | 22992 |
rs377008712 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67127408 | GTACAGGTGTGAGCC[A/G]CTATGCCTGGTGTGC | 22992 |
rs377013543 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67159049 | ATTAATTATTTTTTT[C/T]ATGGATCATGCTTTT | 22992 |
rs377013838 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67182848 | GGAATAAAGTCTTTT[C/T]GAAATGCGTCCAATA | 22992 |
rs377023978 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67186631 | TCTTAACAATGGCTT[C/T]TAACTCCTTTTTGTT | 22992 |
rs377030762 | snp | C/T | 2.14705e-05 | 0.0032764 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | KDM2A | GRCh38.p7 | 11:67219289 | TCCCCTTCTCCTAGG[C/T]TGGATTCATGCTGTG | 22992 |
rs377089276 | snp | C/G | 1.67489e-05 | 0.00289381 | intron-variant | KDM2A | GRCh38.p7 | 11:67243132 | TTAGGCTGCTTAAGC[C/G]TTTTGTTAGTTGATC | 22992 |
rs377097797 | in-del | -/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67211641 | AAAAAAAAAAAAAAA[-/G]AATATATATATAATA | 22992 |
rs377116306 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67211613 | GTGAGACCCTGTCTC[-/A]AAAAAAAAAAAAAAA | 22992 |
rs377122421 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67147585 | TGGATTTCAAGAGCC[A/G]GTGAACCTAGTTAAA | 22992 |
rs377126019 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67122468 | AGTAGCTGGGACTGT[A/C]GGCATGTGCCACCAC | 22992 |
rs377131486 | snp | C/G/T | 3.32758e-05 | 0.00407885 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67254236 | AGCTCCGGAACATGA[C/G/T]CGACTTCCGGCTGGC | 22992 |
rs377136367 | snp | C/T | 0.000150851 | 0.00868348 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67207520 | GGCAGGGAGTCGTCG[C/T]ATGGTGGATGTCATG | 22992 |
rs377210244 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67149225 | TGGTGGAGTCCCTTC[C/G]AGGTTCTAACATTTG | 22992 |
rs377217175 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67208686 | TGAGGCATGAGAATC[G/T]CTTGAACCTGGGAGG | 22992 |
rs377220456 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67235583 | GCTGGAATTACAGGC[A/G]TGACACCGCGCCCGG | 22992 |
rs377220515 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67166433 | TCAAGTGATCCGCCC[A/G]CCTTGGCCTCCTAAA | 22992 |
rs377264894 | in-del | -/AA | 0.00318978 | 0.0398085 | intron-variant | KDM2A | GRCh38.p7 | 11:67199332 | CTCTCACTTTAAATC[-/AA]AAGTTAGAAATGATT | 22992 |
rs377328190 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67135287 | TGGTCAGGATGGTCT[C/T]GATCTCTTGACCTCG | 22992 |
rs377352888 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67171940 | CCAGTCTTGATTACT[A/G]TATGTTTATAGTAAG | 22992 |
rs377392660 | snp | C/G | 3.71092e-05 | 0.00430735 | intron-variant | KDM2A | GRCh38.p7 | 11:67248275 | AACATCTCTGTCTTC[C/G]TATAGATGGACGGAG | 22992 |
rs377406272 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | KDM2A | GRCh38.p7 | 11:67139572 | TTAGAGATGGATCTG[G/T]CTACGTTGGTTGCCC | 22992 |
rs377408006 | in-del | -/GAA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67196910 | ACAAGTTGAAAAAAA[-/GAA]AATAGACTCCTGGAT | 22992 |
rs377420514 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67253879 | AGTCTGAGAAGGCTT[C/T]ATGGTGGAGGTGGAG | 22992 |
rs377424313 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255136 | TCCTCGACCCTGCAC[A/G]GGCTCTGAGGCCAGC | 22992 |
rs377444009 | snp | G/T | 0.000435869 | 0.0147562 | intron-variant | KDM2A | GRCh38.p7 | 11:67181313 | TAATATTTTCCTATG[G/T]TGACAGATTTTAATG | 22992 |
rs377451762 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67174677 | ATATAGTTAATTACG[A/G]CTAAACTGGGAATGG | 22992 |
rs377498028 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67200059 | CTAGATGATATCACA[G/T]CTGTTTTACAGCATG | 22992 |
rs377545137 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67221249 | GATGTTTGTAAGTTA[C/G]TCTCAAGTAGCTTAG | 22992 |
rs377547810 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67159140 | TTTTAGAAGTTTTAT[A/G]GTTGTGTGATTTTCA | 22992 |
rs377568864 | in-del | -/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67202359 | GAGAGGATTGACTCC[-/C]AATTTTGAAAGACGT | 22992 |
rs377617779 | in-del | -/GTTTTGTTTTGTTTT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67198783 | GTTTTGTTTTGTTTT[-/GTTTTGTTTTGTTTT]TGACGGAGTCTCACT | 22992 |
rs377662699 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67222715 | ACCCATTCTAAGATT[C/G]AGTCTGAAAATTGGT | 22992 |
rs377664120 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67248419 | GAAAGGAGGCATCAA[A/T]TGTGGGGGATTGCTA | 22992 |
rs377673417 | in-del | -/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67168584 | CTTGTATGAATTATA[-/C]ACACACACACACACA | 22992 |
rs377697797 | snp | C/G | 3.41245e-05 | 0.0041305 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67250160 | GCGGAGCTGCGATGA[C/G]CCTCTCACGCCCCCG | 22992 |
rs377710923 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67195431 | AATATTCTTCAAGGT[A/G]GTTGGATTGCTGGTG | 22992 |
rs377757335 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67221001 | ATTAATACGTCAGCA[C/T]ATTACCTGTCTGACC | 22992 |
rs386754464 | multinucleotide-polymorphism | CA/TC | | | intron-variant | KDM2A | GRCh38.p7 | 11:67192471 | TTTTTTGAGATGGAG[CA/TC]TCTCTCTTGGTGCCC | 22992 |
rs386754465 | in-del | GTC/TGGT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67192480 | ATGGAGCATCTCTCT[GTC/TGGT]GCCCTGACTGGAGTG | 22992 |
rs386754466 | multinucleotide-polymorphism | AGG/TGA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67192488 | TCTCTCTTGGTGCCC[AGG/TGA]CTGGAGTGCAGTGGC | 22992 |
rs386754467 | in-del | ATA/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67192785 | CTACAATGAAGGTTT[ATA/T]AATTTCTTCTTGGGT | 22992 |
rs386754468 | multinucleotide-polymorphism | ACA/GCC | | | intron-variant | KDM2A | GRCh38.p7 | 11:67216995 | CACGCCTGTAATCCA[ACA/GCC]CTTTGGGAGGCCAAG | 22992 |
rs386754469 | multinucleotide-polymorphism | AT/TC | | | intron-variant | KDM2A | GRCh38.p7 | 11:67235333 | TTTTGAGACTGAGTT[AT/TC]ACTGTTTTTGCCCAG | 22992 |
rs397699717 | in-del | -/A | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67198001 | AAAGTAAGATAAAAA[-/A]TTCCTTAAATCATAA | 22992 |
rs397849065 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67197177 | TATCAGAAATAAACT[-/T]TTTTTTTTTTTTTTG | 22992 |
rs398016493 | in-del | -/A | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67168972 | TGAGACTCCATCTCA[-/A]AAAAAAAAAAAAAAA | 22992 |
rs398016494 | in-del | -/A | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67197191 | GCAATACCCTGTCTC[-/A]AAAAAAAAAAAAAAA | 22992 |
rs398016495 | in-del | -/CA | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67242303 | TTTCTCTCTCTCTCT[-/CA]CACACACACACACAC | 22992 |
rs398045241 | in-del | -/T | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67128033 | TTTTTTTTTTTTTTT[-/T]AGGCGGGGTCTTGCT | 22992 |
rs398045242 | in-del | -/T | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67130142 | AATTTTTTTTTTTTT[-/T]CTTGCACCAAAGCTT | 22992 |
rs527261745 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67225126 | AGCCATCACGCCCGG[C/G]GGCTGCAGCATTTAC | 22992 |
rs527268476 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67213001 | TCAATGTTCTGGGAC[C/T]GGCGGATGCTTGGTT | 22992 |
rs527291471 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67178676 | CTTTTTTTTTATTTG[A/G]CATAATGTTTTCAGA | 22992 |
rs527292314 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67191042 | AATTTAAGAGGGAAC[A/G]CTTCTTTTTTTTCTT | 22992 |
rs527299556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67169544 | GCCACCATACCTGGC[C/T]AATTGTTTTTTGGTA | 22992 |
rs527339334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67125462 | TCATTTTTTGGGGGG[A/G]AAAAAAAATCAGAAA | 22992 |
rs527351987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67133234 | CCTCCCAGGTAGCTG[A/G]GATTACAGGCGTGCG | 22992 |
rs527377318 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67177942 | GCATTTTTTAGTTCT[A/G/T]CTGTAATCTCATGGG | 22992 |
rs527400391 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67132699 | GCTTGCCTTTTGAGG[G/T]GACAGGAACCCTGAA | 22992 |
rs527439607 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67170613 | AGAAACGGGGTTTCA[C/T]CATGTTAGCCAGGAT | 22992 |
rs527470740 | in-del | -/C | 0.00438332 | 0.0466095 | intron-variant | KDM2A | GRCh38.p7 | 11:67176073 | CTTATCAAAATTAAA[-/C]CTTCTTTTGGCTTTT | 22992 |
rs527515648 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67250026 | GAGGTCCACCCTGTC[A/G]GTTCAGAGGGTTTGG | 22992 |
rs527515826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67146553 | TCACTTTGTTATCCA[C/T]GCTGGAGTGCAGTGG | 22992 |
rs527518726 | in-del | -/AC | 0.0112895 | 0.0742785 | intron-variant | KDM2A | GRCh38.p7 | 11:67168547 | TATGAATTATAATAC[-/AC]ACACACACACACACA | 22992 |
rs527529204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67168668 | ACACACACACACGGT[C/T]GGGGGGATAGACAGC | 22992 |
rs527538113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67201284 | TAGTGATTCTGCTGG[C/T]AAATCTGGACCAAAT | 22992 |
rs527575750 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67201861 | TTGGGTGGCTGAGGT[A/G]GGAGGATCACTTGAG | 22992 |
rs527605527 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | KDM2A | GRCh38.p7 | 11:67258539 | CTCCTGACCTCAGGT[A/C]ATCTGCCCGCCTCCA | 22992 |
rs527605785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67154772 | GGAATCATACAATAT[A/G]CTGTATGACCTTTTG | 22992 |
rs527611911 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | KDM2A | GRCh38.p7 | 11:67146003 | GTTTTTTTTTGTTTT[G/T]TTTTTTTGAGACAGA | 22992 |
rs527615907 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67249518 | GTGGGCTCCAGGAAA[A/C]GACAAGTATCTAGAG | 22992 |
rs527622256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67208043 | CTCAAAAATTTAAAA[C/T]AAAATGCGTTGTTTT | 22992 |
rs527633685 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67200729 | CCAGGCTGGTTTAGA[A/C]CTCCTGGGCTCAAGG | 22992 |
rs527645280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67153983 | TAAATGTTTTAGCTG[C/T]CTCTCCTAAGAATAA | 22992 |
rs527646014 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67257563 | CAAGCACCGGGGCGA[A/G]AAACCACAAAGGAAA | 22992 |
rs527655202 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67198670 | AGCTGAGATCCCGCC[A/G]CTGCACTCCAGCCTG | 22992 |
rs527658784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67207262 | GGATTAAATGAGACA[C/T]TAGATAAAAGAGTCA | 22992 |
rs527747120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67216066 | GAATTGTCCCCATTC[A/G]TATCTGGAAAGAATT | 22992 |
rs527767347 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67168269 | TGTCCAGTGAAGTTA[G/T]GCTGAATGAATCAGC | 22992 |
rs527790240 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67223548 | GCTGGGACCACAGAC[G/T]CACACCACCACACCT | 22992 |
rs527853825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67177156 | AGAGAATCCCAGCTA[C/T]TCGGGAGGCTGAGGC | 22992 |
rs527877259 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67230633 | CCTGTCTCAAAACAA[A/G]CAAACCACAACATAA | 22992 |
rs527916664 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67130595 | GAATTGATACATTAT[A/G]TATATCATGTAGATA | 22992 |
rs527972995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67184207 | GGGATTTAAAGGGCT[A/G]TTGTGGCCGGGTGCA | 22992 |
rs528006466 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67138670 | CCTGTAATCCAACCT[A/T]CTAGGGAAGCTGAGG | 22992 |
rs528006627 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67128364 | AATGGACTAGATAAA[A/G]TAGAATATTTATTTT | 22992 |
rs528010005 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67183604 | ATAAAGTACAGTTAA[G/T]TTCAGTCAGTTTCAG | 22992 |
rs528020936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67191635 | GTATTTGACAAAATT[C/T]AACACCTTTTCATGA | 22992 |
rs528045085 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67161368 | CTAGTGTATCACAAA[A/C/T]GTTTAGTTTTCAGTC | 22992 |
rs528055512 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67138096 | CCACCGCGCCTGGCC[A/G]AACTATAGTATTATT | 22992 |
rs528095846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67190979 | TGGTGAATTCTACCA[A/G]ACATTTAAAGAGGAA | 22992 |
rs528111084 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67199900 | TTCAAGGGACAAGTT[A/G]ACTCTCTTGTTAGGG | 22992 |
rs528117140 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | KDM2A | GRCh38.p7 | 11:67144835 | CCTCCCAAAGTGCTG[C/G]GATTATAGGTGTGAG | 22992 |
rs528125881 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67256252 | TGTCTCCCGCTCCAC[C/T]GCCCTTTGTTGAGCC | 22992 |
rs528127887 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67247158 | GCAGTGGCGTGACCT[C/T]GTCTCACTGCAACCT | 22992 |
rs528133077 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67199132 | GAGGTGCCATGAACT[A/G]TATCCATATAGGAGA | 22992 |
rs528135663 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67158637 | TGCAACTCCCTAATG[A/G]TGTACAATGTTCAGC | 22992 |
rs528172823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67191253 | GATGGTCTCGATCTC[C/T]TGACCTCGTGATCTG | 22992 |
rs528193430 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67151953 | GTTTTGTTACATTGC[C/T]CTGGCCTGAAATGGC | 22992 |
rs528198230 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255534 | ACTCTCCCGGCTTGC[A/G]CAGGAGGGGCCAGCA | 22992 |
rs528203120 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67222792 | TGGGTCTTATACACT[C/G]GTTCAGTTTCAGGGA | 22992 |
rs528220557 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67205654 | TGTTTAATTTTTTTT[C/G]TATTTTTAGTAGAGA | 22992 |
rs528229147 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67158901 | TTTAAAAGTTGATTG[A/T]AAATTTTGAGTATTA | 22992 |
rs528229245 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67151050 | AGGATATCATGGTGG[A/T]TAGTAGAAGCAGGGG | 22992 |
rs528271949 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67205424 | CAGGGTATCAGGTTC[A/T]AATGCTACCTGATAC | 22992 |
rs528353692 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67221792 | CTGGGCAACAAAGCC[G/T]GGTGTGGTGGTGCAT | 22992 |
rs528356731 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | KDM2A | GRCh38.p7 | 11:67165999 | ATGACTTAACAGTTG[C/G]ATCAATTATAAAAGG | 22992 |
rs528401581 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67221146 | AGAGCTTATTTTTTA[G/T]CAGAATTCTAATTGG | 22992 |
rs528408707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67122138 | TTTGAAGAGTGGGCT[A/G]TGAGGAAAGCGACAG | 22992 |
rs528463931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67128910 | TTTTCTTGAATGCTA[A/G]GATTAAGCCACTAGA | 22992 |
rs528482651 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67121547 | TTTTATATTTTATAT[A/G]TTTATCTTGTTTGGA | 22992 |
rs528489087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67137272 | GGCATTATCCTGAAG[C/T]CATTGGGAAGGCAGA | 22992 |
rs528514647 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67122396 | CAGTGGCGTGATCTG[A/T]GCTCACCGCAGCCTC | 22992 |
rs528580383 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67155391 | ATGGTTCATTGCAGC[A/G]TCATACTCCTAGGCT | 22992 |
rs528584320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67135593 | AAGGCAGTAATCTGC[A/G]TAAATGACTCGTTTC | 22992 |
rs528593391 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67120015 | TGGAATCTTTTACTT[C/T]TCACTTGGACAAGAA | 22992 |
rs528616012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67244590 | CAAAGGGCTAGGACA[A/G]GGGCTGGTAAATTTT | 22992 |
rs528618322 | snp | C/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185595 | AGGTCACACCATTGA[C/T]TCCCTTGCACTCTAG | 22992 |
rs528633934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67189331 | GGAAATTAGAAAATA[C/T]TTATAGATGAATGAA | 22992 |
rs528657895 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67138562 | GAGGTGGGCAGATCA[G/T]CAGAGGTCAGGAGTT | 22992 |
rs528659702 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KDM2A | GRCh38.p7 | 11:67143362 | CAGGACTTCAGGAGC[A/G]CTAGCATCGGTATGA | 22992 |
rs528684946 | in-del | -/A | 0.460877 | 0.134278 | intron-variant | KDM2A | GRCh38.p7 | 11:67129908 | AGAGACTCTGTCTCA[-/A]AAAAAAAAATTAAAA | 22992 |
rs528690290 | snp | A/G | 0.00478085 | 0.0486577 | upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67119188 | GGCCTGAAGGGGGTG[A/G]GGGGGTGGAGAGGCG | 22992 |
rs528702449 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67197219 | TGCTTTGTCACCCAG[A/G]CTGGAGTGCAGTGGG | 22992 |
rs528703194 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67182829 | TGAGCCACTGCACCC[A/G]GCTGGAATAAAGTCT | 22992 |
rs528728065 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67142593 | GGTTGGGGTTGGGGT[G/T]GGGGGGGCGTCAAGG | 22992 |
rs528737615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67253251 | GTATTGCTCTGGTGG[A/G]AACTAAGCAATCAAT | 22992 |
rs528744293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67196400 | CTGCTTTAACCTCTT[A/G]CATAGCTGGGACTGC | 22992 |
rs528762686 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67217637 | TTGCCTTTCTTCTAC[C/T]TGGTGGTCTTAATTT | 22992 |
rs528799331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67212442 | ATAACTGAGAGGTAG[A/G]TTTTAAAATGGCACA | 22992 |
rs528828059 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67203376 | ATATCTCCAAGATAT[G/T]GTTATACTAAGTAGT | 22992 |
rs528837756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67211345 | TAAGCCAGGTGCGGT[A/G]GCTCACGCCTACAAT | 22992 |
rs528923549 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67218885 | GAGTGCTGGGATTAT[A/G]GGCGTGAGCCCCCGC | 22992 |
rs528931243 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67164494 | TTGTTGTTGTTGTTT[C/T]TTTGTAGCGATGGGA | 22992 |
rs528965113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67171981 | ACTATAGTTTTATAG[C/T]GAGTTCTTCACTCTT | 22992 |
rs528967400 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67197678 | TTCTGTGATAGGATG[C/T]ATTTGGTTGAGAATA | 22992 |
rs529015990 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67119597 | CTCCCGCCCTGTCCG[C/T]CCCCCGGGGCCGGGG | 22992 |
rs529044060 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67242680 | CCACCACCACCATCC[A/G]CCCCCAGTAGAGATG | 22992 |
rs529055682 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67171155 | GCTTAAGCTGTCCTG[A/G]AAAAATAGCCTTTAA | 22992 |
rs529059484 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67194437 | TGAATTACTAACAAC[A/G]TGTTCTTTTCTTAAG | 22992 |
rs529078725 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67225975 | GAGGCTGAGGCAGGA[C/G]AATCGCTTGAACCCA | 22992 |
rs529088609 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67220460 | TATCTTTTTCTACAC[C/T]GATGACTATACTCAA | 22992 |
rs529147726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67187683 | GGTTCAAGCGATTCT[C/T]CTGCCTCAGCCTCCC | 22992 |
rs529161337 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67133970 | GTGCTAGGATTAGAG[C/G]CGTGAGCCACCATGC | 22992 |
rs529187445 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67195472 | TCTTTTTAAACTCTT[C/G]TATTTTCCAAATTTT | 22992 |
rs529187488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67186907 | GACCCATTTCTTCCA[C/T]CCCATGAATGAATGA | 22992 |
rs529195018 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67141433 | GCACTTTGGGAGGCC[A/G]AGGCGGGCGGATCAT | 22992 |
rs529225449 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67133270 | ACACTGCGCTAATTT[G/T]GTGTTTTTTTTTGTA | 22992 |
rs529263263 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67147928 | GTGATTCACCTGCCT[C/T]GACTTCCCAAAGTGC | 22992 |
rs529271696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67194639 | TTGCCTAGTAAAAAA[C/T]AGAGGGCTCTCAGTG | 22992 |
rs529294715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67202612 | CCCGTCTCTACTAAA[A/G]ATACAAAAAAAAAAC | 22992 |
rs529341382 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67134884 | CATGCTTTGCAAAAG[G/T]AAGCATGAAGCCCTT | 22992 |
rs529349760 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67202113 | ACTGCAAATGTGGTG[A/C]AAATAGTGAGAGAGC | 22992 |
rs529365654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67155578 | CAGGTTGCTGGGATT[A/G]CAGGAGTGAGCCACT | 22992 |
rs529367739 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67124404 | GCAACCTCTGCCTCC[C/G]AGGTTCAAATGATTC | 22992 |
rs529382401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67202543 | TTTGGGAGGCTGAGG[C/T]GGGTGGATCACAAGG | 22992 |
rs529406513 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67122586 | CCTTGGCCTCCCAAA[A/G]TGCTGGGATTACAGA | 22992 |
rs529421617 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67154950 | TTGTTTCTACCTTTT[A/C]GCTACTGTGAATAGT | 22992 |
rs529425689 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67157611 | TTAGCCAGACACAGT[A/G]GCACGCGCCTGAAAT | 22992 |
rs529428074 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67208760 | TGTGTGACAGTGAGA[A/C]CCTGTCTCAAAAAAA | 22992 |
rs529487068 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67217157 | TGAGGCAGGAGAATC[A/G]CTTGAACCCAGGAGG | 22992 |
rs529490821 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67155523 | TGCCCAAGCTGGTTT[C/T]GAACTCTTGGCCTAA | 22992 |
rs529506863 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67188683 | GTAGTCTAAGCTACT[A/C]AGGAAGCTGAGGTGG | 22992 |
rs529569572 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67169385 | CTTTCTTTTTCTTTT[C/T]TTTTTTTTTTTGAGA | 22992 |
rs529574144 | snp | C/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185815 | GTGCTTTCTCTCATT[C/G]TCTTACTGTCTCGCT | 22992 |
rs529576792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67216691 | TTTGGGAGGCCAAGG[C/T]GGGCGGATCAGCTGA | 22992 |
rs529652370 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67124809 | TGTGCTATCTTAGCA[G/T]TGTTTGTGTAAGAGG | 22992 |
rs529657551 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67177870 | AAGCATTGCCACAAA[C/T]GAGAGTAATGTGTTG | 22992 |
rs529666780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67177283 | AAAAATATTACTACT[A/G]CTAGTAATAAAACTA | 22992 |
rs529668973 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67218085 | GTTTTCCAATAAAGT[A/G]TATGAGAATTGCCAG | 22992 |
rs529676545 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67166803 | TGTGCTGGGCTGAGC[A/G]TGGTGGGTCATGTCT | 22992 |
rs529687298 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67230880 | TTGTTTTGTTACTTA[C/T]GTTGTTAGAATTTCA | 22992 |
rs529700227 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67139993 | ATAGGCGTGAGCCAC[C/T]GCACCTGGCCTACTC | 22992 |
rs529723692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67240529 | TGCACTTGTTCCCTC[A/G]CCTGGTGGGATGTGC | 22992 |
rs529750960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185146 | AACAAAATGGAAATA[C/T]CAATAAAGAGACAGA | 22992 |
rs529755145 | in-del | -/TGTC | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67143600 | TTTTAGTTTCGCTTT[-/TGTC]TGTCTGTCTTTCTCT | 22992 |
rs529757216 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67249998 | TCTTCTCTCTGGTCC[C/G]CTGAGAGCAAGGGAG | 22992 |
rs529759478 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67139500 | TTCGCCCACCTCGGC[C/T]CCCCAAAGTGCTAGG | 22992 |
rs529764919 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67239485 | TTTGGAACACATAGG[C/T]AGATTCTGGATTGTG | 22992 |
rs529809103 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67257130 | ATAAAAGGGGAGGTG[G/T]AGAGACCCCTTCAGA | 22992 |
rs529883302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67145963 | TCTGGTATATAAAAT[A/G]CCTGTTCTTCCCGTT | 22992 |
rs529924305 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67200709 | ACACAGTTTGACCCT[A/G]TTACCCAGGCTGGTT | 22992 |
rs529928588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67153817 | AGACCCTGTCTCAAA[A/G]AAAAAAAAAAAAACA | 22992 |
rs529950763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67207072 | TATGGATACTTCATT[C/T]AAATTATGAGATAGA | 22992 |
rs529982910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206418 | AGCCTGGGTGACACA[A/G]CGAGACTGTCTCAAA | 22992 |
rs530070337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67159841 | TTTGCAGTTTAGGAT[A/G]TGTTCATATCAGAAA | 22992 |
rs530100451 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67223065 | GGCGTGGTGGCACAT[A/C/G]CCTGTAATCCCAGCT | 22992 |
rs530119513 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67174978 | GGCTGCTAAAATCAC[A/G]TATATGAAAAGCATC | 22992 |
rs530172565 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67122904 | ATGGTCTCGATCTCC[G/T]GACCTTGTGATCTGC | 22992 |
rs530183714 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67123823 | CTGAGATTACAGGTG[A/C]CTACCACCACACCTG | 22992 |
rs530193916 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | KDM2A | GRCh38.p7 | 11:67214361 | GGGCGCCCGCCACCA[C/T]GCCTGGCTAATTTTT | 22992 |
rs530197477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67166781 | AAACTGAGCAGGTCA[A/G]AACTCCTGTGCTGGG | 22992 |
rs530200350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67175481 | CACTGTTGCCAACTT[C/T]CCAGTTGCAATAATC | 22992 |
rs530202565 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67212552 | ATATTGGACTTCTTA[C/T]CAGTTTGGCCCTAGT | 22992 |
rs530204253 | in-del | -/A | 0.209388 | 0.246679 | intron-variant | KDM2A | GRCh38.p7 | 11:67208769 | GTGAGACCCTGTCTC[-/A]AAAAAAAAAAAAAAA | 22992 |
rs530204933 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67251946 | GCACATCAGATTCCC[A/G]TTATGTGCTGTCTCT | 22992 |
rs530213538 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67229924 | GCTCACACCTGTAAT[A/C]CCAGCACTTTGGGAG | 22992 |
rs530241886 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67247289 | GAGATGGGGTGTCAC[A/C]GTGTTGGCCAGGCCG | 22992 |
rs530260710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67236735 | AATTAACAAGATTAG[C/T]AAAATACTTAATAAG | 22992 |
rs530326970 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67243647 | GGTGAAACACCGTCT[C/G]TACCAAAAATACAAA | 22992 |
rs530351204 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67199055 | AAAGTGCTGAGATTA[A/C]AGGCATGAGCCACTG | 22992 |
rs530353237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67190173 | CCAGCACTTTGGGAG[A/G]CCGAGGCGGGTGGAT | 22992 |
rs530443403 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67187731 | GGTGCCCGCCACCAC[A/G]CCCGGCTAAATTTTG | 22992 |
rs530475004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67205265 | TCTTTTAAAATATGA[A/G]GTGTAGGTTCTGTCC | 22992 |
rs530481046 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67245859 | GTTCTCTCCACCCTG[C/G]CTCCATGCTTCCAGG | 22992 |
rs530534952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67158133 | CATACACCAGCAACT[A/G]CGGATCTTTTTGCTG | 22992 |
rs530542399 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67205614 | TTGTATTTGTATTTG[C/G/T]ATTTTTTTGTTTTGT | 22992 |
rs530548124 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67235690 | GCAGTGGCGCCATCT[C/T]GGCTCACTGCAGCCT | 22992 |
rs530564418 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67254769 | AGTTGTGGGACAAAG[A/G]GGGCTTTTGTTTAGC | 22992 |
rs530597460 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67223171 | CACTCCAGCCTGGGC[A/G]ACAAGAATGAAACTC | 22992 |
rs530680141 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67204531 | GAGTCTCACTGTGTT[G/T]CCCAGGCTGGAGTGC | 22992 |
rs530684420 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67157623 | AGTGGCACGCGCCTG[A/T]AATCCCAGCTACTCG | 22992 |
rs530696069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67173391 | CCTCCCAAAGTGTGG[A/G]GATTACATGCGTGAG | 22992 |
rs530711133 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67220986 | TTGAACCTTGTTACT[A/G]TTAATACGTCAGCAC | 22992 |
rs530722288 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67122071 | TTGTTTTTCTTAGCC[A/G]AAGAGAGCTTTATTA | 22992 |
rs530749893 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | KDM2A | GRCh38.p7 | 11:67128095 | CCACTGCAGCATCAG[A/C]CTCCCCAAGTGATCC | 22992 |
rs530798273 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67228427 | CCGGACACGCTGGTT[C/G]ACGCCTGTAATCCTA | 22992 |
rs530827939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67227592 | TTGTTGTTGTTCAGA[C/T]GGAGTCTCACTCTGT | 22992 |
rs530838696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67244403 | CAAGACTAGTTTCAC[C/T]TTAAGGGAGTTTACT | 22992 |
rs530875259 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67143260 | GATCCTCCCGCCTCC[G/T]CCTCCCAAGGTGTTG | 22992 |
rs530905502 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67133261 | TGCGCCACCACACTG[C/T]GCTAATTTTGTGTTT | 22992 |
rs530917887 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67226928 | TGGGTGAAAGAGCAA[C/G]ACCCTGTCTCTAAAA | 22992 |
rs530922809 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67147394 | AAAAATAAAGAAAAT[G/T]AGCCGGGTGTGGTGG | 22992 |
rs530934800 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67180811 | GCACGTGCCACCACA[C/T]CCGGCTAATTTTTTT | 22992 |
rs530935586 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67142328 | AGGCATGAGCCACCG[C/T]GCCCACTGTATATCT | 22992 |
rs530959280 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67178717 | GTCATGGCACATAGC[A/G]TTATTTCATTCCTTT | 22992 |
rs530962239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67234583 | ATTAAAAAGTACTGA[C/T]TTGGGCTGAGCCCAG | 22992 |
rs530965543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67253176 | TTGGTCAGCTCCTTA[C/T]AAGCCCTTGTTCTCT | 22992 |
rs530983584 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67151849 | TCCTGGGCTTAAGCA[A/T]TTCTCTTACCTCAAC | 22992 |
rs531001796 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67148841 | AAGAAATAATCCACA[C/G/T]CCTAAAGTGCGATTC | 22992 |
rs531015826 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67197033 | TTCCTCGGTAATCTT[C/G]TTACTGCTAATAATG | 22992 |
rs531049744 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67214783 | GGTCTATCTTAGTTT[C/T]ATAGATGAGTTTGAG | 22992 |
rs531053606 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67252445 | TCAAACACTCCAGAA[A/T]AAATCAGGGTAAAGT | 22992 |
rs531054752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67196287 | TTCATGTCAGCCAGA[C/T]GGCAGGAGGGAGCAA | 22992 |
rs531071663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67211243 | GATGTTCAGTAAAGT[A/G]GACCCCCATTTTAAG | 22992 |
rs531142572 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67203322 | GACTTGCTTACTGGA[A/G]TAGTTGCTTTATTGC | 22992 |
rs531181093 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67202913 | GGTGGAAGGATTACC[A/G]GAGTCCAGGAGTTTG | 22992 |
rs531184891 | in-del | -/AA | 0.0575206 | 0.159536 | intron-variant | KDM2A | GRCh38.p7 | 11:67129907 | CAGAGACTCTGTCTC[-/AA]AAAAAAAAATTAAAA | 22992 |
rs531197131 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67119313 | TGCTTCAGCGGCTCC[C/T]CCTGTGTGAGGGAAA | 22992 |
rs531261250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67126695 | CCTGGGCGACAGAGC[A/G]AGACTCCATTTCAAA | 22992 |
rs531277992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67225917 | TAAAAACATAAAAAT[C/T]AGCTGGTCATGGTGG | 22992 |
rs531279754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67217440 | AGCCAGACAGAGTGT[C/T]TAAGGGACTGCCTAG | 22992 |
rs531283532 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67163025 | ATGATTTCTTTTTCT[C/T]AAAGTTAGGAATTGA | 22992 |
rs531287108 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67179461 | TATTTTTAGTAGAGA[C/T]ATGGTTTCTCCGTGT | 22992 |
rs531298279 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67236224 | CAGCCTCCGCCTGTC[A/G]GGTTCAAGTGATTCT | 22992 |
rs531316156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67225202 | CATCACTCTAGTATA[C/T]TGACTTTGAAAACAA | 22992 |
rs531319874 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67133922 | TGGTCTCAAACTCCT[A/G]ACCTCGTGATCCTCC | 22992 |
rs531323377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67217981 | GTTATGATGCTGGGC[A/G]TCTGCAGAAAACAAC | 22992 |
rs531334179 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | KDM2A | GRCh38.p7 | 11:67217547 | GTTGGATCAAGTGAA[A/G]GATAAGAAAGATCTA | 22992 |
rs531369200 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67198442 | AAACCTTTTCATTAT[C/G]CCGGGCGCAATGGCT | 22992 |
rs531373204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67187644 | CAGTGGTGCAGTCTC[A/G]ACTCACTGCAACCTC | 22992 |
rs531400023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67232921 | CACCATGTTGGCCAG[A/G]CTGGTCTCGAACTCT | 22992 |
rs531410594 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67170353 | TTACCCCAGGGAAGA[G/T]CCTTTGCTAATCCTT | 22992 |
rs531491135 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67170969 | TTACTAGCTTTGTAA[C/T]CTGGGCAAGTTACTT | 22992 |
rs531502215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67178738 | TCATTCCTTTTTGTG[A/G]TTAAATGATATCTCA | 22992 |
rs531524108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67240641 | CTGTAGGGTGTGGGC[C/T]TGTGTTTAAATGTTC | 22992 |
rs531528916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67202017 | GAGGTCAAAATATCA[A/G]CATTAACAGGAGTTT | 22992 |
rs531561473 | snp | A/C | 9.71713e-05 | 0.00696966 | intron-variant | KDM2A | GRCh38.p7 | 11:67250047 | GAGGGTTTGGAAGAA[A/C]GGAAGCACTGATGTT | 22992 |
rs531567867 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67241293 | TTCACCCCCACGCTG[A/T]ATGGTACTAACAGAA | 22992 |
rs531574764 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67140798 | TTTATTTATATTAAC[C/T]TTTCTGTCTCTAGTA | 22992 |
rs531653777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67251107 | TGAGAGTCTTGCGGG[C/T]TGAAAATTTCCTCCT | 22992 |
rs531662835 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67147300 | GTAATCCCAGCACTT[C/G/T]GGGAGGCCGAGGCGG | 22992 |
rs531791797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67208085 | ATTTTATAACTTTTT[A/G]CACATATCAAGATTA | 22992 |
rs531797542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67216150 | AGTTCACTGTCATTA[C/T]ACCATTGGCACAGCA | 22992 |
rs531825970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67168412 | TTAAATTGTAATTCT[A/G]TAATTTATTTACATA | 22992 |
rs531838832 | in-del | -/TCTTGGCTATGAGTGAAAGGG | 0.0138799 | 0.0821421 | intron-variant | KDM2A | GRCh38.p7 | 11:67241419 | CTTAGTAGAGGAGCT[-/TCTTGGCTATGAGTGAAAGGG]TCTTGGCTATGAGTG | 22992 |
rs531864434 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67177214 | GAGGTTGCAGAGAGC[C/T]GAGATCACTCCATTG | 22992 |
rs531883259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67216607 | GAACTAGAATGAGAA[C/T]AGATAATGCCTTGTT | 22992 |
rs531927525 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67224325 | AAGAAAGCTGTATGG[A/C]CAGATATGGTGGTTC | 22992 |
rs531978250 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67215241 | AAATTATAGTTTTTT[A/G]TTATGTATTTTAAGA | 22992 |
rs531993863 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67124543 | GTGTCGAACTCCTGA[A/C]CTCAGATGATCACCC | 22992 |
rs532017583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67223817 | ACCCTTCCAGAAAGT[A/G]TTGCTATACTTAAAA | 22992 |
rs532017705 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67184377 | GTTGACGCCTGTAAT[C/G]CCAGCACTTTGGGAG | 22992 |
rs532039802 | snp | C/G | | | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67119932 | TCGCTCTGACCCTCT[C/G]TGGATACTGGGTTGA | 22992 |
rs532048141 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67138736 | CAGCGAGCCAAGATT[A/G]TGCCACTACATTCTT | 22992 |
rs532055283 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67230758 | AAGGGATGACTTATT[G/T]ACCGCTTTGCGCCTT | 22992 |
rs532059169 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67124012 | GTTTGTTTGTTGGTT[G/T]GTTTGTTTTGAGACT | 22992 |
rs532065271 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67133332 | GTCTCAAACTCCTGA[C/G]CTCAAGTGATCCACC | 22992 |
rs532097896 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67256468 | TAAATGATTGATGCA[A/G]ATTTGCACTCTGCTC | 22992 |
rs532128463 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67239345 | CAGACATTTCTAGTA[A/C]TGTACTGTGGGGGTG | 22992 |
rs532129398 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67248052 | CAGTGGAGAACACTG[A/C]GTCACAGAGACTAGA | 22992 |
rs532131911 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67256389 | AGGTCGGAATTTCTT[C/T]TGGGTCAATATTTTT | 22992 |
rs532136096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67152767 | TATGGATCATTCCAT[A/G]GCAGATGTTTAATGA | 22992 |
rs532140384 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67192775 | ACAAATAATGCTACA[A/G]TGAAGGTTTATAAAT | 22992 |
rs532143125 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67230072 | TCCCAGCTATTTGGG[A/G]GGCTGAGGCAGAAGA | 22992 |
rs532165046 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67249092 | AGGAATTTTCTTACT[G/T]TTTATTTCTTCCCAC | 22992 |
rs532177951 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67238199 | AGCAGGAGGGGGTAA[A/G]GTTAGGCCTTGTTTA | 22992 |
rs532223053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67152040 | TAATTTCCCGCCGGG[C/T]GCAGTGGCTCACACC | 22992 |
rs532362994 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67146795 | TGCATGAGCCACCGT[A/G]CCTGGAACATTCTTT | 22992 |
rs532368044 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206338 | TGGGAGGCTGAGGCA[C/G]AAGAATCTCTTGAAC | 22992 |
rs532381617 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255596 | ACTGGTGCTGTTGAG[A/G]TCTCCCAAACCTCAC | 22992 |
rs532386117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67221916 | CTCCAGCCTGGGTGG[A/G]AGAGTGAGACACAGT | 22992 |
rs532395856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67215157 | TATTCTCATATAACA[A/G]TTATTTCTAGGATGG | 22992 |
rs532481763 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67228634 | AGGCTGCAGTGAGCC[A/G]AAGATCATGCCACTG | 22992 |
rs532482020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67236681 | AATTTATGGAAACCT[A/G]TTTTCTCCTCTATAA | 22992 |
rs532500622 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67174377 | TCAAAAGTTCTGATT[A/T]CCCAACTCTTACCTG | 22992 |
rs532512409 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67128993 | GAGGTTGAGGCAGAA[A/G]TATCATTTGAGCCCA | 22992 |
rs532518888 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67176262 | TTCATTTTTTATGAC[-/T]TTATTTCTGCCCTTT | 22992 |
rs532560100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67175418 | CCCAGCCTAGATGAC[A/G]GAGACTCTGTCTCCG | 22992 |
rs532560601 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67242334 | AGAAAGAGATTTGAG[A/G]TTGAGATTTCTGTAA | 22992 |
rs532574712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67136701 | GGTTCTGGGGACCAG[A/G]TCTGGGGCCCTAGGT | 22992 |
rs532594634 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67211694 | ATTTTTTAATATTCA[A/G]AAACTTAATCTTCAT | 22992 |
rs532601416 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67189928 | AATAACTAGAAAAAG[C/G]ACAAACTAAACCTAA | 22992 |
rs532614538 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67246670 | GCTCCCCTACTGATC[A/C]GAATTGTGCAGCCTT | 22992 |
rs532627164 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67245643 | TAGTACTAAAAATCC[A/G]ATTTAATCTTTAGGC | 22992 |
rs532632677 | snp | C/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206239 | AGTTTGAGACCAGCC[C/T]GGCCAACATGGCAAA | 22992 |
rs532648842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67183361 | TTCCCTCTTGATGAG[A/G]CATTCTTACAGATTG | 22992 |
rs532697911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67205162 | TGCATTTTTGCTAGC[A/G]CTCATTATTTTCCAT | 22992 |
rs532739782 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67141351 | TTCAGGTCCTCCTCT[C/G]AAGCTATTTTGAAAT | 22992 |
rs532754306 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67145880 | TACATCCTTTGGGAA[-/T]TTTTTTTTTTTTTAA | 22992 |
rs532761061 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67161077 | TGGACAAGGTGGACT[A/G]GTGGCCAGGCACAGT | 22992 |
rs532782334 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67204352 | AGCAGTCATTCTCCG[C/T]TTTCTCCTCCACTTA | 22992 |
rs532794627 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67143954 | AAACTATTTTTTTTT[G/T]TTTGTGAGACGGAGT | 22992 |
rs532831111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67189388 | GGGATCAGTGAAAGC[A/G]ACATTAAAGGAGAAA | 22992 |
rs532835984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67157616 | CAGACACAGTGGCAC[A/G]CGCCTGAAATCCCAG | 22992 |
rs532857741 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67143394 | ATAGTGTTGGTTCAG[A/T]TTCTGAAAATTTCTT | 22992 |
rs532859653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67244707 | CAGCCATTGATTGGC[C/T]GGGTGTGGTGGCTCA | 22992 |
rs532873777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67164889 | CATGTGTGAGCACCG[C/T]GCCTGGCCTGCTATT | 22992 |
rs532875597 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67167246 | GTTGAGATGCCTTAT[C/G]CTCATCTTGAATTGA | 22992 |
rs532878754 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67150639 | TCCTTTGAGAGGAGG[G/T]ATCTAAGAGTTGGAG | 22992 |
rs532907763 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67211487 | GGTGTGGTGGTGCAC[A/G]CCCGTGATCCCAGCT | 22992 |
rs532913170 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67201486 | CTACAAAAAATTAGC[C/T]ATGGCCCGGTGCGGT | 22992 |
rs532916385 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67149814 | CAACCTCGGCCTCCC[A/G]GGTTCAAGTGATTCT | 22992 |
rs532928481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67220330 | TCTTGGATTTTTATA[A/G]GGCCAGACATTTACC | 22992 |
rs532971280 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67172177 | TTTTTTTTTGTAGAG[A/G]CAGTGGCTGGTCTTG | 22992 |
rs532997948 | in-del | -/TT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67197884 | GAATTCCTCAGAAAC[-/TT]AACTACCAATAACCT | 22992 |
rs533033455 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67157282 | CGCGCCACTGCACTC[C/T]ATCCAGCCTGGGCGA | 22992 |
rs533058205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67232854 | CTGAGATTACAGACA[C/T]GTGCCACCATGCCTG | 22992 |
rs533089864 | snp | A/G | 0.00039885 | 0.0141162 | intron-variant | KDM2A | GRCh38.p7 | 11:67121401 | CTCCAGTTTTAAAGT[A/G]GGATAACTATTTTGT | 22992 |
rs533109075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67188216 | GGGCGCAGTGACTCA[C/T]GCTTGTAATCCCAGC | 22992 |
rs533122105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67163975 | ATTACTAGTTAAGTA[A/G]GTCAGACACAGTGAG | 22992 |
rs533125598 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67229391 | GAGAAATATTTTAAT[C/T]AGATGACAGTGTAGT | 22992 |
rs533152713 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67142245 | TTTGACCATGTTGGT[C/T]AGGCTGGTCTCAAAC | 22992 |
rs533192521 | snp | A/C | 0.00019363 | 0.00983755 | intron-variant | KDM2A | GRCh38.p7 | 11:67196224 | CGAGCAGGGGCTTGC[A/C]GCCCATGAGCCTCAG | 22992 |
rs533207193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67253038 | CAGTCTCCCAGGCAG[C/T]ACTCTGGACTGGCAG | 22992 |
rs533224141 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67226895 | TACTGGGGAGGCTTT[C/G]GTGGGAGGATGATAG | 22992 |
rs533240566 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67191288 | CCTCGGCCTCCCAAA[A/G]TGCTGAGATAACAGG | 22992 |
rs533293164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67211342 | AAATAAGCCAGGTGC[A/G]GTAGCTCACGCCTAC | 22992 |
rs533302621 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67248132 | ATCAGGTTCAGCACC[A/T]TTGGCTATTTGGGGC | 22992 |
rs533340191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67134043 | TTGTTGAAGTTGTAC[A/G]GTGTGCTTTCTGAGG | 22992 |
rs533388326 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67160898 | GAATTGCTTGAGCCC[A/G]GGAGTTCAAGTCCAA | 22992 |
rs533395753 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67155683 | GTGCAATGGCTTGAT[C/G]TTGGCTCACTGCAAC | 22992 |
rs533403094 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | KDM2A | GRCh38.p7 | 11:67242304 | TGTGTGTGTGTGTGT[C/G]AGAGAGAGAGAGAAA | 22992 |
rs533423042 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67195552 | CTCTGTTACTATAAA[G/T]AAAATGGTTTTCAGG | 22992 |
rs533490728 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67252223 | GGTGAATTGTGGATG[A/T]GCTGAGTAGCACCCT | 22992 |
rs533535725 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67216748 | CAACATGGAGAAAGT[G/T]CATCTCTACTAAAAA | 22992 |
rs533585541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67202167 | ATGCGACTGAATTGC[C/T]GCAATCTATAATGAA | 22992 |
rs533685613 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67167974 | AAGTTTTATATAGAT[C/G]AAAAGATAAAAACTT | 22992 |
rs533699353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67169272 | TCCATGTAGCTTTAT[A/G]TAACTTTACAAAACA | 22992 |
rs533719494 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67131913 | AGGCTTTTATTTATG[G/T]ATGTCACTCATATCC | 22992 |
rs533753661 | snp | A/G | 4.47918e-05 | 0.00473222 | intron-variant | KDM2A | GRCh38.p7 | 11:67207733 | ATTGTCACCAAAAGG[A/G]TTGTTTTCGGCTGGA | 22992 |
rs533773904 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67239586 | ACTCAGCTCCTGTGC[C/G]TAGTTCATCCAGAGA | 22992 |
rs533778753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67230303 | CAGCTTAGGCAACAT[A/G]GTGACACCCCCATCT | 22992 |
rs533781336 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67131881 | ACGGCAGTATTGTGC[A/G]GTTTGTGTGTATGTC | 22992 |
rs533792219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67161078 | GGACAAGGTGGACTA[A/G]TGGCCAGGCACAGTA | 22992 |
rs533819427 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67129463 | GCATAGGCCGGGCGC[A/G]GTGGCTCACACCTGT | 22992 |
rs533821015 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67165593 | CCAGAGAGAAGGATC[A/G]TGTAGGAAAGCTTCC | 22992 |
rs533843705 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67216302 | AAGGGAACACGAATT[C/T]TGGATAGATTCACTG | 22992 |
rs533859191 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67238458 | GTTAAGGAAAGCCTT[C/T]CAAACAAAATAAGCC | 22992 |
rs533893891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67248462 | TGCATTAGTGTTCAC[A/G]CAGTTTCTCTGACCT | 22992 |
rs533906478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67138410 | TATTCACCTACAAGG[C/T]TCTTAGTTCTAATAA | 22992 |
rs533922740 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67224855 | TTTTTTTTTTTTTTT[G/T]TTGGAGACAGAGTTT | 22992 |
rs533966957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67145161 | ACAGGTGTGAGCCAC[C/T]GTGCCCGACCATTCA | 22992 |
rs533972013 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67145426 | ACCCGGGAGGTGTAG[A/G]TGCCAGTGAGCTGAG | 22992 |
rs533975250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67247420 | TTTAACAGCATTACA[A/G]TCTTTTTTTTTTTTT | 22992 |
rs533991613 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67199508 | CTTATCACTGATAAC[A/G]GAGAAAGTCTGAGTG | 22992 |
rs533999001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67176895 | AGTGAGTAAATGCGA[A/G]GGCCTAAGACACTTT | 22992 |
rs533999045 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185495 | TTAACTGGGCATGGT[C/G]GTGGGCCCCTGTAAT | 22992 |
rs534004787 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67188167 | CCAGCCTGGGTGACA[G/T]AGCCAAGACCCTGTG | 22992 |
rs534053760 | in-del | -/T | 0.081211 | 0.184419 | intron-variant | KDM2A | GRCh38.p7 | 11:67145549 | TATGGTAGCACCCCA[-/T]TTTTTTTTTTCATTA | 22992 |
rs534066935 | in-del | -/TTTA | 0.18989 | 0.242666 | intron-variant | KDM2A | GRCh38.p7 | 11:67187548 | ATTTATTTAATTGAT[-/TTTA]TTTATTTATTTATTT | 22992 |
rs534070563 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67205915 | AGAATTCTACTTATT[A/C]TTCTCCCTCTTTTCC | 22992 |
rs534097826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67139019 | TTTCTAAACCACTAA[C/T]GGTATCTTAGGCACA | 22992 |
rs534120493 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67128631 | TACATCAGTCTTCCA[C/T]AGTAAGCTATATTTT | 22992 |
rs534141210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67191996 | TTTTGCTGTTTGTCA[A/G]ATATTTCAAATATAC | 22992 |
rs534162235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67145677 | GAATTTCTTTCCATT[A/G]TACCATATTCTCCCT | 22992 |
rs534193116 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KDM2A | GRCh38.p7 | 11:67214007 | AGCTAGGACTATAGG[C/T]ACATGCCACAACGCC | 22992 |
rs534213362 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67244342 | TATTGAAGTGTCTGC[C/T]ATCTACCAGTTCGTA | 22992 |
rs534219303 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67202100 | AGTGGAGGAAGTAAC[C/T]GCAAATGTGGTGAAA | 22992 |
rs534231573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67221372 | TGCTCTTGAAACTTT[C/T]TGGTAGAATTAAAAG | 22992 |
rs534232356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67153039 | GCCCAGGCTAGAGTG[A/G]AATGGCACGATCTCA | 22992 |
rs534246442 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67256890 | CTCTGCCCACTTCCA[C/T]TGGTCTCCAGGCCCC | 22992 |
rs534272238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67152232 | GTGGGAGGATCACTT[A/G]AGCCCAGGAGGCGGA | 22992 |
rs534278602 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67125407 | GCTAGTCTTGAACTC[C/T]TGGGCTCAAACGATC | 22992 |
rs534338492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67226876 | ATACACTTGTAATCT[C/T]GGCTACTGGGGAGGC | 22992 |
rs534364188 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67159299 | TACATCCGAGTTACC[G/T]TTGGTCCTGTGTCAA | 22992 |
rs534372552 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67190237 | CAATGTGATGAAACC[A/C]TGTCTCTACTAAAAA | 22992 |
rs534374022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67181994 | TAGGAACATTGAAGT[A/G]TATATTTGATTAGAA | 22992 |
rs534402659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67158494 | CAAGCTGTTTTCCAA[A/G]GTAGCTGTACTATTT | 22992 |
rs534457655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67189568 | ATCTCGGCCGGGCGA[A/G]GTGGCTCACGCCTGT | 22992 |
rs534485352 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67143647 | TTTATTTATTTATTT[A/T]TTTGAGATAGGGTCT | 22992 |
rs534499863 | snp | A/G | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67197548 | GATAGCTAATCATTG[A/G]CAAAATGCAGTGAAA | 22992 |
rs534505609 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67175574 | AGACAGAAGCCTTCC[A/T]TGTATCCTTACATTC | 22992 |
rs534516745 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67229634 | CCAGCACTTTGGGAG[G/T]CTGAGGCGGGCGGAT | 22992 |
rs534552740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67150101 | TGACAGATCTTACAC[A/G]AAATTACAGAATTCT | 22992 |
rs534565052 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67254142 | CTGTTGCTGCCTGGA[G/T]CCTTGAAGCTGGATT | 22992 |
rs534584101 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67204607 | TGCCATTCTCCTGCC[G/T]CAGTCTCCCGAGTAC | 22992 |
rs534589548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67157645 | AGCTACTCGGGAGGC[C/T]GAGGCACAAGGATCG | 22992 |
rs534637726 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67236264 | GCCTCCTGAGTAGCT[C/G]GGATTATAGGTGTGT | 22992 |
rs534648566 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67128612 | AACTAATTTTTTATT[C/G]TTATACATCAGTCTT | 22992 |
rs534657996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67137243 | TGACAAGGTAGACAG[A/G]TCAGATCAAATAGGG | 22992 |
rs534658344 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67123201 | CCCTAGTCTTGAACT[C/G]CTGGCCTCAAGCGAT | 22992 |
rs534670457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67157387 | CGTGTGTGAGTGTGT[A/G]TGATTGACTTTTTAA | 22992 |
rs534727434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67235701 | ATCTCGGCTCACTGC[A/G]GCCTCCACCTCCTGG | 22992 |
rs534761938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67198449 | TTCATTATGCCGGGC[A/G]CAATGGCTCATGCCT | 22992 |
rs534771572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67244885 | CAGCTACTTGGGAGG[C/T]TGAGGCAGGAGAATG | 22992 |
rs534775434 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67254875 | CACTTTCCCGACAGG[C/T]TGCAATAAATTGACA | 22992 |
rs534779684 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67153826 | CTCAAAAAAAAAAAA[A/C]AAAACACCAAAAACA | 22992 |
rs534779967 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67187566 | TATTTATTTATTTAT[C/T]TATTTATTTATTTAT | 22992 |
rs534801944 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67172516 | AAATTTATTCCTTAG[G/T]TTTTTTTATGCTATT | 22992 |
rs534813346 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67127718 | AATTTATTTATTTAT[G/T]TATTTTGAGATGGAG | 22992 |
rs534824625 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67227082 | AGTACCTTTTAAAAT[A/T]AGTATCCAGCTGAAA | 22992 |
rs534868267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67127134 | ACAGGGTCTCACTCC[A/G]TTGCCCAGGCTAGAG | 22992 |
rs534871739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67134919 | TGTTGTTGAATTTTC[A/G]CAAAACTAACTTCAT | 22992 |
rs534913690 | snp | C/T | 0.000112155 | 0.00748764 | intron-variant | KDM2A | GRCh38.p7 | 11:67219417 | GGGTAAGTAATCTTA[C/T]GTAACAGTTGCATGT | 22992 |
rs534921308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67212745 | TGACTTTCTTGCTGC[A/G]ATTAAGAAATTCTGC | 22992 |
rs534929814 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67147944 | GACTTCCCAAAGTGC[A/G]GGGATTATAGGTGTG | 22992 |
rs534966011 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67145816 | CTGAATCATACATTT[G/T]CCTTCCTCTCTAACT | 22992 |
rs535008081 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67242803 | AGTTTTGATAATATT[A/G]CAGCAGCCTAAGTTT | 22992 |
rs535010619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67220536 | CTGGGGTTTCAAGAG[A/G]GAATTAAGCCCAAAA | 22992 |
rs535010780 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67211986 | TATATAAACTATAGT[A/G]TGAGCAGTGCTTCAA | 22992 |
rs535013430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67142060 | TCATTCATTTTTGAG[A/G]CGGAGTCTTGCTGTG | 22992 |
rs535044069 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67252470 | TAAAGTGGTCAAGTT[A/G]TATACTATCAACATG | 22992 |
rs535052729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67195852 | TTCAAAGCTGGTTCC[A/G]TTGCCAGTATTTTAT | 22992 |
rs535126231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67251839 | ATTTCCCAAATCTGA[A/G]TTAATGTATAGTGTA | 22992 |
rs535135003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67120261 | GCAAGCACGGTTTCC[C/T]TCCCGACTTCGGGCC | 22992 |
rs535144543 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | KDM2A | GRCh38.p7 | 11:67210349 | TTTTGAAAAAAAAAA[A/C]AAAAAACAAAAACTA | 22992 |
rs535160903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67180851 | ACTTTTAGTAGAGAC[A/G]GGGTTTCGCCATGTT | 22992 |
rs535216408 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67226460 | AGGCGCAGTGGCTCA[C/T]GCCTGTAATCCCAGA | 22992 |
rs535242255 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67204192 | CCATCATAACCATTA[C/T]GTTTTTTTCTTTTTG | 22992 |
rs535255598 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67188326 | TCTCTACTAAAAATA[C/G]AAAATATTAGCCGGG | 22992 |
rs535262151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67217486 | GTCCCTCTTCTCTCC[A/G]AGTCCTGGATGGTGT | 22992 |
rs535263728 | in-del | -/AC | 0.00716266 | 0.059414 | intron-variant | KDM2A | GRCh38.p7 | 11:67213108 | TTGTTTCTTCCATGT[-/AC]CAGTGGTGATGCTTT | 22992 |
rs535267200 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67159290 | CTACCTTTCTACATC[C/T]GAGTTACCTTTGGTC | 22992 |
rs535286795 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB, synonymous-codon | KDM2A, LOC107984341 | GRCh38.p7 | 11:67118062 | GTCGGGCCGGGGGCC[A/G]GGGGCGGCCCGCGCA | 22992 |
rs535297586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67216982 | GGGCACAGTGGCTCA[C/T]GCCTGTAATCCAACA | 22992 |
rs535298208 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67170413 | TTCTTTCTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 22992 |
rs535345177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67126205 | GAGCTGAGATCATGC[C/T]GTTGCACTCCAGCCT | 22992 |
rs535377565 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67224992 | GATTACAGGTATGCA[A/C]CACCACGCTAATTTT | 22992 |
rs535384247 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67178827 | TTTCTATCTTTTGGC[G/T]GTTGTGAATAACACT | 22992 |
rs535407443 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67200820 | CCTGAGATTAATACC[A/G]TTTTCATGCCAGATA | 22992 |
rs535479696 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67220624 | ACCCTTCTAGATGCA[A/T]AGAAAAAAGTTAATT | 22992 |
rs535481821 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67186391 | CAAAACTGTCAACCA[A/T]GCATCCTATATCTGG | 22992 |
rs535488945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67156596 | TGGTGGTAGGCGCCT[A/G]TAGTCCCAGCTACTC | 22992 |
rs535490923 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67128778 | GAGAGTTGGGGCTTT[A/G]TTTTTGTTTATGCTG | 22992 |
rs535504898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67202376 | ATTTTGAAAGACGTT[C/T]TACCATGGGTAAAAT | 22992 |
rs535518616 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185669 | TTATCCCTTCCAAAA[C/T]TTATGTTGAAATTGA | 22992 |
rs535556413 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67239971 | GAACACACCCCCTCC[C/T]GGCTCTGCAGCAGAA | 22992 |
rs535593907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67146804 | CACCGTGCCTGGAAC[A/G]TTCTTTAATATTGGT | 22992 |
rs535601997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67193221 | TCTTGAACTCCTGAC[C/T]TCAGGTGATCCACCC | 22992 |
rs535649810 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67156991 | CCCACAAAATTTAAA[A/C]TATTTACCCTCTGGC | 22992 |
rs535657092 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67257874 | TAGTTGGACTTTGTT[C/T]TGTTTTCCAAAAGTT | 22992 |
rs535672022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67144182 | ACTCCTGATGTCACG[C/T]GATCTGCCTACCTCC | 22992 |
rs535679522 | in-del | -/CAATCAAGAAATATCCCAAAACGTT | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67149010 | GCATGGTTAATAAGC[-/CAATCAAGAAATATCCCAAAACGTT]CATTTTTGCTTCCTT | 22992 |
rs535727701 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67160895 | GGAGAATTGCTTGAG[C/T]CCAGGAGTTCAAGTC | 22992 |
rs535734944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67169813 | CTCAGGCTAGAGTAC[A/G]GTGGCGAGATCTCGG | 22992 |
rs535763088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67125644 | GGGCACTGGGGGTGG[C/T]GGTGCGTGCCTGTAA | 22992 |
rs535777397 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67178265 | AAAAAAATCAGCTGG[G/T]TGTGGTGGTGTGCAC | 22992 |
rs535778116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206822 | TGCTGACTCTTGTGG[C/T]CTTATGCGTTTTGTT | 22992 |
rs535795798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67232370 | TCTATGCTGGGTTAA[C/T]GTTGAGTAGCTTTAG | 22992 |
rs535831878 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67132894 | GGTGATTTTGATCCA[A/C/T]GCAAAAGTTTGAGAA | 22992 |
rs535846188 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67182928 | TCTATTATCTTTTGT[C/T]CTCTGTACTAAAGCT | 22992 |
rs535931048 | snp | C/T | 1.71546e-05 | 0.00292865 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67250151 | GCGGCCCCTGCGGAG[C/T]TGCGATGAGCCTCTC | 22992 |
rs535944136 | in-del | -/TT | 0.00597247 | 0.0543191 | intron-variant | KDM2A | GRCh38.p7 | 11:67201246 | GTGTATATATATATA[-/TT]TTTCATAAGGCTATA | 22992 |
rs535960226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67139671 | GGCATGAGCCACCAC[A/G]ACTGGCCCAAAGGTT | 22992 |
rs535964087 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67176489 | GGTATGTATTCAATA[A/T]ATTTCAGCAAATTTT | 22992 |
rs536000020 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67213622 | AAATTAGTTAGGTGC[A/G]GTGGCGGGTGCCTGT | 22992 |
rs536000713 | snp | A/G | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67146197 | ACAGGGTTTCACCAT[A/G]TTGGCCAGGATGGTC | 22992 |
rs536015407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67229795 | GAATCACTTGAACCC[A/G]GGAGGTGGAGGTTGC | 22992 |
rs536020991 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67130424 | TGTTGGGATTACAGG[A/C]GTGAGCCACCATGCC | 22992 |
rs536022694 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67138830 | CAACTAGTTCTCCAG[A/G]TGATTCTGATAGATG | 22992 |
rs536022996 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67249843 | GAGACGCAATTAAAA[A/T]TGGTCAGGCCAGGTG | 22992 |
rs536057766 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67257871 | AGCTAGTTGGACTTT[C/G]TTTTGTTTTCCAAAA | 22992 |
rs536079459 | snp | C/T | 4.6822e-05 | 0.00483826 | intron-variant | KDM2A | GRCh38.p7 | 11:67248248 | AGGAAGCTTGAGAGA[C/T]AGGCTTTTAAAAACA | 22992 |
rs536080002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67183847 | GGCACAGTGGGTCAT[A/G]CCTGTAATCTTAGCA | 22992 |
rs536087693 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67138253 | TTCAGGTGCTCAAAA[C/G]TTGTCTATTGAATTG | 22992 |
rs536096210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67237028 | GAGTGAGAGTGGCAG[A/G]GTCTATCCTGAGGGA | 22992 |
rs536117482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67247326 | AACTCCTAACCTCAA[A/G]TGATTCACCCGCCTT | 22992 |
rs536141869 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67257106 | TTTGTTTTATTTTGT[C/T]GTCTTTTTATAAAAG | 22992 |
rs536210303 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KDM2A | GRCh38.p7 | 11:67246369 | AGCTTAGAATCTGGA[C/T]TCTGGATTGGGTATG | 22992 |
rs536231189 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | KDM2A | GRCh38.p7 | 11:67177139 | CTCGGGAGGCTGAGG[C/T]GAGAGAATCCCAGCT | 22992 |
rs536245629 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255126 | GGAGAGCCTCTCCTC[A/G]ACCCTGCACGGGCTC | 22992 |
rs536246352 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67215702 | CCTTTTTCTGATAAT[C/G]TGATGACTTGAAAAT | 22992 |
rs536256216 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67144513 | CACCTCAGCCTTCCA[A/C]AGTGCTGGGATTACA | 22992 |
rs536257072 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67179713 | CTGTGAAAAAATTAT[A/G]TTTTGTATCCTGGCT | 22992 |
rs536292323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67151487 | CCGAATAAGTGGGGT[C/T]ACAGGTGTCTGCCAT | 22992 |
rs536321215 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67205504 | TAAATTTTTTTTTTC[A/T]ACAGCCTCGACCTCC | 22992 |
rs536343650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67176827 | GTATAGGGCACTTCT[C/T]GTGATGGGTTTTGCA | 22992 |
rs536349239 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67213834 | TTTAATCCTTACAAC[A/G]TATCTTTGAAGTAGT | 22992 |
rs536382407 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67184454 | CCAACATGGTGAAAC[C/G]CCGTCTTTACTAAAA | 22992 |
rs536392650 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67123983 | GACCTGGACTTTTGG[A/G]TTTTGTTGTTGTTGT | 22992 |
rs536396825 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67238253 | GGAGTGAGTTTCCTA[A/G]TGCCCGATGTGATTT | 22992 |
rs536474528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67191932 | ACTTTTTTATTTGTT[A/G]TTAGTATTTTTCTTT | 22992 |
rs536475289 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67220679 | GGCAAGAGTTGACAA[A/C]CTTTTCCTGCAAAGG | 22992 |
rs536507471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67121775 | TGTCCCAGGATTTGT[A/G]ACTTTGAGCGGGGAG | 22992 |
rs536536106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67173787 | GCCCCATCATAACTC[A/G]TGGCAGCCTCAAGCT | 22992 |
rs536544335 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67202879 | ACGTGCCTGTAGTCC[C/T]AGCTACTCCGGAGGC | 22992 |
rs536555198 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67144999 | CTCAGCCTCTCAAGT[A/T]GCTGGGTGTAGAGGC | 22992 |
rs536568186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67128542 | GCGGCCTCCCTCCTA[A/G]TAATGTAGGAAAAAC | 22992 |
rs536593085 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67156075 | ACCAATGTGGAGAAA[C/G]CCCGTCTCTACTAAA | 22992 |
rs536593086 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | KDM2A | GRCh38.p7 | 11:67235604 | CCGCGCCCGGCTGCT[G/T]TTTTGTTTTGTTTTG | 22992 |
rs536688458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67159165 | TTTTCATTTAGGCCT[A/G]TGATCTTTTTTGAGT | 22992 |
rs536690985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67244767 | AAGGCGGGCAGATCA[C/T]GAGGTCAGGAGATTG | 22992 |
rs536692335 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67144692 | CCTCAGCCTCCTGAG[G/T]AACTGGGAGTACCGG | 22992 |
rs536710727 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67197466 | TACAGGCGTGAGCCA[C/G]TCTGCCCAGCCAGTG | 22992 |
rs536724812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67158416 | TTTTGTGTGGACATG[A/G]GTTTTCAATTCATTG | 22992 |
rs536800201 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67149106 | AAGCTCTTTAATAAT[C/G]GCAAAAGTTAAAAAG | 22992 |
rs536808831 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67166166 | AAATTGGTTGACTTT[C/T]AGGAGAAACAATATT | 22992 |
rs536809224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67157741 | CAAAAGCAAGACTCC[A/G]TCTCCAAAAAAAAAA | 22992 |
rs536812617 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67137039 | GCTTTGAAGTTGAGA[A/C]CTAAAGGGTGACTAG | 22992 |
rs536825309 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67171840 | GCTTACTGAAAATCA[A/G]TTCACTGTAAGTGTA | 22992 |
rs536840687 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67203790 | GCTTTCCTCTACATT[A/C]TTTTTTTTTTTTTTC | 22992 |
rs536842274 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67165345 | CAGGCTGGTCTTGAA[C/G]TCCTGACCTCAGATG | 22992 |
rs536846204 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67169696 | CTTGGTTTCTTTTTT[A/C]TTTCTTTTTTCTTTT | 22992 |
rs536853421 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67122427 | CACCTCCTGGGTTCA[A/G]GTGATCCTCCTGCCT | 22992 |
rs536859734 | snp | A/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67207058 | GTTACCCACTAAATT[A/G]TGGATACTTCATTCA | 22992 |
rs536889843 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67157329 | TCTCAAAAAAAAAAA[A/C]AACAAAAAACACCAC | 22992 |
rs536911875 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67211768 | CTTCTCACTTTATAT[C/T]CTCAAGTTCTAACCT | 22992 |
rs536912691 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67129268 | TGGACCATTTAGAAC[A/C]AATAATAAAGTGTCT | 22992 |
rs536928670 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67164222 | GACCCAGACCTACTT[C/T]TGACTCTAATCCATT | 22992 |
rs537004658 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67120541 | TATTTTCCTTGTATC[C/T]TTAGATGCAATCGTT | 22992 |
rs537028995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67136042 | GATTTTTTCACCAGG[C/T]CAGAAACCATTTTTG | 22992 |
rs537033306 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67127948 | CGACCTCAGGCAGGC[A/G]ATCTGCCTGCCTCGG | 22992 |
rs537052802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67171553 | TAGAAAAAGTGACAC[C/T]AGATATATTTTCCCT | 22992 |
rs537089956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67135111 | TTCACTTTTGTTGCC[C/T]AGGCTGGAGTGCAAT | 22992 |
rs537090387 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67153489 | GGATTCATGCAATAC[A/G]TTTTCCCCAAACCCT | 22992 |
rs537092737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67234854 | TGAGACCTTGTCTCA[A/G]AAAGAAAGTAGGCCG | 22992 |
rs537111709 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67127066 | TTTGATGCTGGGGTG[G/T]GTTGTTCTGAGGTAA | 22992 |
rs537120137 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67254099 | CAGTTCTACTTAACC[C/G]CTTCAAGGGGGCCTG | 22992 |
rs537125635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67244111 | AGAGAATCACCTCCT[C/T]GTCCCTAGTGGGAGG | 22992 |
rs537139489 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67179666 | GTGTTTTTGAGATTG[C/T]TTTACCAAGCTAATT | 22992 |
rs537152857 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | KDM2A | GRCh38.p7 | 11:67142941 | TCTCTATCTTCTACT[C/G]CCTCTCAGTTGTCTT | 22992 |
rs537162302 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67233600 | AAGGTTGCAGTGAGC[C/T]GAGATTGCGCCATTG | 22992 |
rs537166596 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67149949 | CAGGTCTTGAACTCC[C/T]GACCTCAGGTGACCT | 22992 |
rs537207446 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67180892 | GTCTCGAACTCCTGA[C/T]CTGAGGTGATCTGCC | 22992 |
rs537293489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67148509 | TTCCCCCATCAGAAA[C/T]AAGTAATCCGGCCGG | 22992 |
rs537306560 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67145484 | GAGTGAGACTTCATT[G/T]TAAGAAAAAAAGATA | 22992 |
rs537322992 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67172338 | AAGCTGTGATTTTGA[A/T]AAGAATTGCTTTGAA | 22992 |
rs537325851 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67213092 | GTTGCTCCTCATCTT[A/G]TTTGTTTCTTCCATG | 22992 |
rs537329518 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67251696 | GGGGACTCTGATGCA[C/T]GCTCGAGTTTAGAGC | 22992 |
rs537330778 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67156837 | GAGGTTGCAGTGAGC[C/T]GAGATCGCGCCACTG | 22992 |
rs537353181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67210733 | TTTTGTGACCTTGCT[A/G]TGTAAGTAATAACGT | 22992 |
rs537387775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67120940 | CTTGCTGATGCTGCC[A/G]TGAAGGAGATCCTTG | 22992 |
rs537396459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67155762 | GCTGTGATTACAGGC[A/G]TGTGCCACCATACCC | 22992 |
rs537397060 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67216797 | TGGTGGTACATGCCT[A/G]TAATCCCAGCTACTC | 22992 |
rs537401875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67147010 | GGTTAATTTGTAGCA[A/G]TAGTTAAAATTTGCT | 22992 |
rs537410660 | snp | A/G | 9.16045e-05 | 0.00676711 | synonymous-codon, intron-variant | KDM2A | GRCh38.p7 | 11:67250787 | GCGAGTGTGCAAGAC[A/G]TGGTATAAATGGTGA | 22992 |
rs537429598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67218371 | CCTGCTAGATACTAC[A/G]CTTAGAGCAAATATT | 22992 |
rs537430299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67209004 | GCGGTGGCACGATCT[C/T]GGTTCACTGCAACCT | 22992 |
rs537452382 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67244463 | CAGGATGAGGAAATA[C/T]TGGAGGGCTCCTGGA | 22992 |
rs537503648 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | KDM2A, LOC107984341 | GRCh38.p7 | 11:67118563 | TGCGCCCTCTCGCCC[C/T]GGGCAGGCCTGAGCC | 22992 |
rs537577377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67126478 | TTTGGGAGGCTGAGG[C/T]GGGTGGATCACCTGA | 22992 |
rs537602275 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67145162 | CAGGTGTGAGCCACC[A/G]TGCCCGACCATTCAC | 22992 |
rs537632460 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67216348 | AAGATCTAAACCAAC[A/T]TTCCCTCTATGTAGC | 22992 |
rs537642428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67125523 | ACACCTGAAATCCCA[C/T]CACTTTGGGAGGCAT | 22992 |
rs537656099 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67173873 | ACCATGCTCAACTAA[G/T]TTAAACAATTTTTTT | 22992 |
rs537676723 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67224152 | AAAAGGGACTCCTAT[C/G]CAGTTCTCCGTGATT | 22992 |
rs537676855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67232109 | TTGTTATTGCTGCTC[A/G]GTGTTTTCATTACTA | 22992 |
rs537690246 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67175416 | ACCCCAGCCTAGATG[A/G]CAGAGACTCTGTCTC | 22992 |
rs537692202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67194810 | ATTCACCTGCTGTTG[C/T]AGCAGGGTTTTAGGA | 22992 |
rs537693013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67241796 | AGATTTGGCCAGGTG[C/T]AGTGGCTCATGCCTG | 22992 |
rs537780750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67194278 | CCTTTCCCAAACTGG[A/G]GGAGGGTGGTTGCTT | 22992 |
rs537790284 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67148854 | CACCCTAAAGTGCGA[C/T]TCAGCTGAAATTGTC | 22992 |
rs537815955 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67201725 | GTGAGCCAAGATCAC[A/C]CCACCCCACCACACT | 22992 |
rs537859986 | in-del | -/AAAC | 0.00318978 | 0.0398085 | intron-variant | KDM2A | GRCh38.p7 | 11:67211058 | TGAGACCCTATTTCA[-/AAAC]AAACAAACAAACAAA | 22992 |
rs537863133 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67165830 | AACCTTTCTTGACTG[A/G]CAAAAAGAAAGGTCA | 22992 |
rs537865265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67184552 | AGAATTGCTTGAACC[A/G]GGAGGCAGAGGTTGC | 22992 |
rs537886787 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67155159 | AGCTGGGGTTGCAGG[G/T]GCCTGCCACCACACC | 22992 |
rs537894102 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67238566 | AGGAGAAGCTCAGCC[A/G]AGAGCACAAAAGTCT | 22992 |
rs537906069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67192241 | CTTGGTTTTTAATGC[A/G]GTCTGTAGACATGCA | 22992 |
rs537925724 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67161593 | GTTTTCTGATTTACT[A/C]AAATTTCATTTAAAA | 22992 |
rs537950608 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67198832 | TGCCCAGGCTGGAAT[A/G]CAGTGGCACAATCTT | 22992 |
rs537983210 | in-del | -/CAAA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67204316 | AGAATTTCATCACCC[-/CAAA]CAAACTCCATACCTT | 22992 |
rs538006472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67169604 | TGCTCTTGAACTCCT[A/G]ACCTTAGGTGATCCT | 22992 |
rs538025850 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67256511 | GATACTGATAGCACA[A/G]CCTCTTCCCCCCACC | 22992 |
rs538035442 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206771 | CTTAGGTCTCTTTGA[C/T]TCCAAAGCTATTGTT | 22992 |
rs538038932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67178102 | CATACCATACAGTCT[C/T]CTCATTTAAAGTGTA | 22992 |
rs538094798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67152362 | GGCTCACACTTGTTA[C/T]TCCAAGTATTTTGCG | 22992 |
rs538103773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67125220 | ATAGGGGTCTTTGTC[A/G]CCCAGTCTAGAGTGC | 22992 |
rs538125645 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67167598 | TATCTTTTTTTTTTT[C/G]CTTAAAGGTCCTACT | 22992 |
rs538130559 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67134715 | TCGCCACGTTGACTA[A/G]GCTGGTCTCGAACTT | 22992 |
rs538133730 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67159454 | TTGGATCTAGAAGAT[G/T]AGATTCATCTTAAAC | 22992 |
rs538168726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67214735 | CCTTGGCCTTCCAAA[A/G]CTCTGGGATTGCAGG | 22992 |
rs538212521 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67169130 | CTGGCCAATTTTTGT[A/G]TTTTTAGTAGAGATG | 22992 |
rs538214277 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67176198 | TTTTGCCTAAAACTT[C/G/T]TAAGTTGAATCTTGC | 22992 |
rs538229886 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67139605 | GCTGGTCTTGAACTC[A/C]TAGGCTCAAGTGATC | 22992 |
rs538248481 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255284 | AGCAGATTGATCTGA[A/G]GGGAAAGCACAGGCT | 22992 |
rs538248793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67175768 | GGTTTGAAAACATGA[A/G]GGATTTTTAAAACAA | 22992 |
rs538253663 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67222280 | GGTGATGACTCTTAA[C/T]GAGCATGCTGCCTTC | 22992 |
rs538253931 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67193051 | CTGGAGTGCAGTGCC[A/G]CGATCTCGGCTTACT | 22992 |
rs538268916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67146136 | AGCTGGGATTTCAGG[C/T]GCATACCACCACACC | 22992 |
rs538278713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67249643 | GGTTCTTGTTATCTG[C/T]TTTATTATTCACGTG | 22992 |
rs538291495 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67139142 | GAGTACAGAAGGGGC[A/C]CATTACTACGCCCTT | 22992 |
rs538299672 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67167417 | CTCATTTCTTGACCA[A/G]TTAGTTTTGTGGAGG | 22992 |
rs538334744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67175025 | CATGCTAGTAAGCCA[A/G]TTTGTATTATTTGGT | 22992 |
rs538378329 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67129445 | AATACAAAAATTAGC[C/T]GGGCATAGGCCGGGC | 22992 |
rs538380480 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67182925 | ATTTCTATTATCTTT[G/T]GTCCTCTGTACTAAA | 22992 |
rs538381247 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67225726 | GTGAGCCGAGATCAC[A/T]CCACTGGACTCTAGC | 22992 |
rs538388818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67153223 | TTCCTGACATTGGGT[A/G]ATCGACCCGCCTCGG | 22992 |
rs538390483 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67244739 | ACCTGTAATCCCAGC[A/T]CTATGGGATGCCAAG | 22992 |
rs538400703 | snp | A/G | 0.00187758 | 0.0305821 | intron-variant | KDM2A | GRCh38.p7 | 11:67196378 | ATCCTGGACTCAAGC[A/G]ATCTTCCTGCTTTAA | 22992 |
rs538407848 | snp | A/G | 0.00398564 | 0.0444627 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67256980 | TAGGGGAACTTCTCT[A/G]TAAAGAACCCTGGGT | 22992 |
rs538442164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67137308 | AGCAGAGTAGTAATG[C/T]GTTTGGACCAATGTC | 22992 |
rs538495765 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67144292 | AGTCTCACTCTTGTT[A/G]CCCAGGCTGGAGTGC | 22992 |
rs538498739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67246259 | CAGTGGTCTAACATC[A/G]GCCCTTGATTCATAT | 22992 |
rs538540025 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67223148 | AGTGAGCCAAGATCG[C/T]GCCATTGCACTCCAG | 22992 |
rs538557843 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67143696 | GGAGTGCAATGACGC[G/T]ATCTTGGCTCACTGC | 22992 |
rs538596364 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67121001 | GGTGTGGCCCTTCCA[C/G]AAGGAACTGAAACCA | 22992 |
rs538616414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67123261 | GATTAACAAGCGTGA[A/G]CCACAGTACCTGGCT | 22992 |
rs538633056 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67213178 | GACAACTGCTTCATA[C/T]CATGCACAACTTTAT | 22992 |
rs538697420 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67135940 | TAGATAGCTCATCCT[A/G]TCATATACTTTCATT | 22992 |
rs538716711 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67248602 | TTGGGATCTGCAAAT[G/T]CCTAAGGTCCTTTTA | 22992 |
rs538732231 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67212879 | ACTTTATTCATTATT[C/G]TGTTAAAGGCATTCC | 22992 |
rs538736354 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67165286 | CGCCGCCACACCTGG[C/G]TAATTTTGTATTTTT | 22992 |
rs538756854 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67191147 | CTCCTGGGTTCAAGC[A/G]ATTCCCTGCCTCAGC | 22992 |
rs538761473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67228889 | ACACCACTATGCCCA[A/G]CTAATTCTTACTTTC | 22992 |
rs538762372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67121594 | GCCTTTAGCTTTTAT[A/G]GAAACCATTGTATAC | 22992 |
rs538791603 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67236370 | CCTGACCTCAAGTGA[A/C/T]CTGCCTGTCTAGGCC | 22992 |
rs538846573 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67227871 | TTTCTCAAGACCAAC[A/G]TTTTCTAAGTTGATG | 22992 |
rs538877522 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67158455 | CATTTTATGGTAAGA[A/G]TGTTTAGTTTTGTAA | 22992 |
rs538882301 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67235549 | CTCAGATGATCCACC[C/T]GCCTCTGCCTCCCAA | 22992 |
rs538887477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67198526 | AGGAGATCGAGACCA[C/T]GGTGAAATCCCATCT | 22992 |
rs539007978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67213634 | TGCGGTGGCGGGTGC[C/T]TGTAATCCCAGCTAC | 22992 |
rs539087014 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67231093 | TCCCTAGTATCTGGG[A/G]CCACAGTCATGCATC | 22992 |
rs539100903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67203516 | TATAATATATAATAT[A/G]AAATATATAATAAAT | 22992 |
rs539108491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67253376 | ACTGGAAGTTTGTTC[A/G]CTTTGCTCAGATCGT | 22992 |
rs539115927 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67169449 | CAGTGGCACCATCTC[A/G]GCTCACTGCAACCTC | 22992 |
rs539186228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67164637 | TGGACTTTTTTTTTT[C/T]GGAAACGACATCTTG | 22992 |
rs539187978 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67203040 | CGGTTTACACTTCAG[A/C]GAAAGAAAAAGAAGT | 22992 |
rs539201091 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67166267 | TCGGCTCACTGTAAT[C/G]TCTCCCTCCTGGGTT | 22992 |
rs539209818 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67129076 | CTACAGAGCAAGACC[C/T]TGTCTCTAAAAAAAT | 22992 |
rs539222913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67219692 | CCAAGTAGCTGGGAC[C/T]GTGGGTGCACACCAC | 22992 |
rs539231008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67156667 | GAGCTTGCAGTGAGC[C/T]GAGATGGCGCCTCTG | 22992 |
rs539238749 | in-del | -/T/TATATAT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67201203 | GTCTCAAAAAAAAAA[-/T/TATATAT]ATATATATATATATA | 22992 |
rs539239866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67181694 | CCTGTGCATATGTGT[A/G]AATATATAATCACCT | 22992 |
rs539267735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67163168 | CTGTCTTCTAGCGCT[A/G]CACTTTCGTATTTAT | 22992 |
rs539321406 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67209651 | GTTTCACCATGTTGG[C/T]CAGGCTTGTCTCGAA | 22992 |
rs539346111 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67171334 | TGAATGCAACATAAA[C/T]AGACCAGAGGGACTG | 22992 |
rs539349460 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67167036 | TGAATTGAGATCATA[A/C]CATTGCACTCCAGCC | 22992 |
rs539382097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67134472 | TCCTGATTATCTGCT[A/G]TTCATTTTATAATTT | 22992 |
rs539403367 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67142662 | TGAGCCGAGATTGCA[C/T]CATCGCACTCCAGAC | 22992 |
rs539415865 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67192607 | GCAACACCATGCCTG[G/T]TCAATTTTGTATTTT | 22992 |
rs539436586 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67187968 | GGGAGGCTGAGGCAG[G/T]ACTGCTTGAAGCCAG | 22992 |
rs539444712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67142077 | GGAGTCTTGCTGTGT[C/T]GTCCAGGCTGGAGTG | 22992 |
rs539450609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67179088 | TCTTTGATGATAGCC[A/G]TTCTGGTGGGTATAA | 22992 |
rs539465863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67242858 | TATTTGTTTTCCAGT[A/G]AGTCTCTATATGAAG | 22992 |
rs539488626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67133454 | GTTGCCCAGGCTGGA[A/G]TGCAGTGGCCTAATC | 22992 |
rs539527184 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67148474 | TAAAACTCAAATAAT[A/C]GGTATCAATCATATC | 22992 |
rs539539217 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67224440 | AGTGAGACCCTGTCC[A/G]TACCAAAAATTAACC | 22992 |
rs539544850 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67127165 | TGCAGTGGTGTGATC[A/C]TTCCTCTTTGTAGCC | 22992 |
rs539603554 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67251541 | GGTCACACACATCCT[A/C]TTACAGTAGTGTGGT | 22992 |
rs539640552 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67132752 | AGTGTAGGTCTCTCA[C/T]TAGCAGCATGAGCAT | 22992 |
rs539660627 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67126331 | TATATTCCCAGCACT[C/T]CGGGAGGCCAGGGAG | 22992 |
rs539683033 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67155971 | AATCACAGGAAGGGC[A/G]GGGCGCAGGGCTCAC | 22992 |
rs539699491 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67119892 | AGAAGGTTTGATTCA[A/G]CAACTGTTTGCTCCC | 22992 |
rs539728563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67155082 | TGCAGTGGTGCCATC[C/T]TGGCTCACTGCAACC | 22992 |
rs539730847 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67217525 | ACCCAAGGGAAGCCT[G/T]AATGCTGTTGGATCA | 22992 |
rs539819377 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67225569 | TGACGTTGGGAGTTC[A/G]AAACCAGTCTGACCA | 22992 |
rs539854290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67153434 | AATTTGGTTTAATGT[A/G]TCATCAAACTTTGTA | 22992 |
rs539871546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67197023 | CACTTTTCCTTTCCT[C/T]GGTAATCTTCTTACT | 22992 |
rs539879135 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67125735 | ACTAAGCAGAGATTG[C/T]GCCACTGCACTCCAG | 22992 |
rs539915738 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67199960 | ACCAAATTTAACATT[A/C]CAAAAAAAGCTTATT | 22992 |
rs539924308 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67132991 | GGACTGACTAAACTT[G/T]GTAACTGATGGATAG | 22992 |
rs539947476 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67256255 | CTCCCGCTCCACCGC[C/T]CTTTGTTGAGCCCCA | 22992 |
rs539951605 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67160445 | AAGTGATTTTGTGAC[C/G]AGTTTGTTAGGGAGG | 22992 |
rs539959265 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67241550 | GATTATGAGAAAAAT[G/T]ATTAGCAATGGCCCA | 22992 |
rs539963382 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67232397 | TTAGCCTCTTTAGAT[G/T]CAAATTTATCTAGCA | 22992 |
rs540041708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67194054 | ATTTTTAAAATTTAA[C/T]CTCATTTCTTTGAGT | 22992 |
rs540051516 | snp | A/G/T | 0.00159649 | 0.0282165 | intron-variant | KDM2A | GRCh38.p7 | 11:67123632 | TCTAAGGAATTTTGC[A/G/T]GTCCAGACTTTAAAG | 22992 |
rs540073404 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67125481 | AAAAATCAGAAATAA[C/T]TAGTTAAGGACTGGG | 22992 |
rs540137521 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67122799 | TCCTGCCTCAGCCTC[C/G]CGAGTAGCTGGGACT | 22992 |
rs540137790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67130478 | ATCCTGTCCTAAACT[A/G]TGCCTAGGTTTTGCT | 22992 |
rs540145432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67166713 | GTTTGGCATCAATAT[A/G]GTGACCTCCCAGCAA | 22992 |
rs540185533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67175314 | CACACCTGTAATCCC[A/G]GCACTTTGGGAGGCC | 22992 |
rs540197525 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67248847 | ATCCCACATGCCCAA[A/G]TGTGTCATGTGGAGG | 22992 |
rs540198113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67129661 | ATGGTGTGAACCCGG[A/G]AGGCGGAGCTTGCAG | 22992 |
rs540223573 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67229361 | TGTGCTTTCAAGTTT[A/C]CCCAACATCTATCAG | 22992 |
rs540230100 | snp | A/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67257188 | TGACTTTGGGACATT[A/T]CATCCACAGAAATTT | 22992 |
rs540238995 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67160385 | TGCTTTGACCTAGTA[A/C]ATCCTGGGTTCAGGA | 22992 |
rs540241028 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67124257 | GATCCACCCACATCA[A/G]CCTCTCAAAGTGCTG | 22992 |
rs540310558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67246598 | AAGTAATAAAAAGTA[A/G]TAAATTCAGATCTCA | 22992 |
rs540324863 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67157433 | TTTTAAAAGCAAAAA[A/T]ATTCCTGGTTTCTCT | 22992 |
rs540327127 | snp | C/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67184965 | AAATCATAAGGCATA[C/T]GAAGAAAAAGGAAAG | 22992 |
rs540328575 | in-del | -/A | 0.318415 | 0.240457 | intron-variant | KDM2A | GRCh38.p7 | 11:67213756 | AGAGCAGACCGTCTC[-/A]AAAAAAAAAAAAAAA | 22992 |
rs540339997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206313 | GCACACGGCCATATT[C/T]CCAGCTACTTGGGAG | 22992 |
rs540359024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67159722 | TGATAGGTACTGGGA[A/G]GACAGTGGTGAAAAA | 22992 |
rs540360944 | snp | G/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67178273 | CAGCTGGGTGTGGTG[G/T]TGTGCACTGGTGGTG | 22992 |
rs540369142 | snp | A/C | 1.65745e-05 | 0.00287871 | intron-variant | KDM2A | GRCh38.p7 | 11:67228203 | TTGAAGACACCGCTT[A/C]GGTCTGAGGGTGAGG | 22992 |
rs540373591 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | KDM2A | GRCh38.p7 | 11:67258322 | GGAGTCTCGCTCTGT[C/T]GCCCAGGCTGGAGTG | 22992 |
rs540424351 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67215067 | AGTTCATAGTTATAC[A/C]CTATTGCATAATTAA | 22992 |
rs540476171 | snp | A/C | 0.000358972 | 0.0133924 | intron-variant | KDM2A | GRCh38.p7 | 11:67254532 | GACCCACATCAGCTC[A/C]TTTCTTCACATCTGG | 22992 |
rs540490027 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67224872 | TGGAGACAGAGTTTC[A/G]CTGCTGTTGTCCAAG | 22992 |
rs540544988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67229826 | AGTGAGCCGAGATCA[C/T]GCCACTGCACTCCAG | 22992 |
rs540583610 | in-del | -/T | 0.00676609 | 0.0577691 | intron-variant | KDM2A | GRCh38.p7 | 11:67140376 | GTCTCAAAAAAAAAA[-/T]ATCATGGTTTTATAC | 22992 |
rs540620059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67212487 | GTTTGGTGATGGGGA[A/G]ATAAGTTCATGGAAG | 22992 |
rs540647058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67183246 | CGTCACAAGACAGAA[C/T]ACTCAGGGGACCTCA | 22992 |
rs540659774 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67219997 | ACACCATAGTGAATG[C/G]GAAAAAGTAACATTT | 22992 |
rs540693417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67164810 | CACTATGTGGGCCAG[A/G]CTGGTCTTGAACTCC | 22992 |
rs540711585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67144533 | CTGGGATTACAGGTG[C/T]GAGCCACCGTGCCCG | 22992 |
rs540751657 | snp | A/C | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67120867 | GGATCTGGATTAGTT[A/C]AGTGGTGCTTCACCT | 22992 |
rs540765538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67198802 | TGTTTTGTTTTTGAC[A/G]GAGTCTCACTCTGTT | 22992 |
rs540771258 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67189841 | GAGACTCTGTGTCAA[A/C]AAACAAACAAACACC | 22992 |
rs540788794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67227448 | TGCCTTTTTTTCAAG[C/T]ATTTTGTGTCTTACT | 22992 |
rs540800503 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67157172 | CAAAAAATTAGCCGG[A/G]TGTGGTGGTGGGTGC | 22992 |
rs540811484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67188543 | CACGTCTGTAATCCC[A/G]ACTTTGGGAGGCCAA | 22992 |
rs540840667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67150462 | TTTTTGTAGTAATCT[A/G]TAGTATTTTTGGTTT | 22992 |
rs540872235 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67222900 | AGAAAAATAAGGGGG[-/A]AAAAAAAAAAAGGCC | 22992 |
rs540897614 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67188131 | AGGAGTTTGAGGCTG[A/T]TCTGATCACACCACT | 22992 |
rs540928513 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67157842 | TGGGTGTGGGTACCT[A/G]TAGTCTCAGCTACTC | 22992 |
rs540955921 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67165733 | ACAGCATGTGTGACA[A/C]ATTTCATGGTTTTTA | 22992 |
rs540958191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67142139 | CACTTCCCAGGTTCA[A/G]ATGATTCTCCTGGCT | 22992 |
rs540963675 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67157608 | AAATTAGCCAGACAC[A/T]GTGGCACGCGCCTGA | 22992 |
rs541018995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67220754 | ATTGTAACTGTTTAA[C/T]CCTACCTTGTAGCAT | 22992 |
rs541043839 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67173974 | CCTACCCCAGCCTCC[C/G]TAATTGCTGGTATTA | 22992 |
rs541048209 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67203197 | TTTTAGCAATAAAGT[A/T]TTTTTAAATAAAAGT | 22992 |
rs541053744 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67228241 | TACTCAGTAGGCTGT[C/T]ACTCAATATGTTCTT | 22992 |
rs541126218 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67156336 | ACGCCTGTAATCCCA[A/G]CACTTTGGGAGGCTG | 22992 |
rs541126306 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67163377 | GAAGAGATTTAGAGA[G/T]GGAATCATAAAAGAG | 22992 |
rs541133035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67127985 | AAAGTGCTGGGATTA[C/T]AGTTGTGAGCCAGCA | 22992 |
rs541165085 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67162657 | GTGATCCGCCCGCCT[C/T]GGCCTCCCAAAGTGC | 22992 |
rs541194356 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67135167 | TCCGCCTTCTGGGTT[C/G]AAGCGATTCTCCTGC | 22992 |
rs541233510 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67150929 | TCAGTCTAAACCTAG[C/T]GTTGAAGGCCAAAGG | 22992 |
rs541244650 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67119139 | ACGCGTGCGCGTTCA[C/T]GCGCGCCCGGGAGAG | 22992 |
rs541248591 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67143136 | AAGTGATTCTCTTGC[A/G]TCAGCATCCCGAGTT | 22992 |
rs541257593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67134656 | ATTACAGGTATGCGT[C/T]GCCACGCCCAGCTAA | 22992 |
rs541264791 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67234334 | GGGACAAAGCTAGTA[C/T]AGTTTACCCTTCCTG | 22992 |
rs541267737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67126564 | AATACAAAAATTAGC[C/T]GGATGTGGTGGCAGG | 22992 |
rs541278072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67244245 | AAGAAATTAAAGTAG[C/T]AGAAAACATGGTCCT | 22992 |
rs541289686 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67196917 | TGAAAAAAAAATAGA[C/T]TCCTGGATATAGTAT | 22992 |
rs541320101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67243298 | TCTCTTAACAGAACT[A/G]TCAAACTGGGAGGCC | 22992 |
rs541331414 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67133786 | GGCTTACTATAACTT[A/C]CGCCTCCCAGGTTCA | 22992 |
rs541381131 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67233394 | TGCGATGTCTCATGC[A/C]TGTAATCCCAGCACT | 22992 |
rs541385995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67241897 | AACATGGTGAAACTC[C/T]GTCTCTACTAAAAAT | 22992 |
rs541390329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67133176 | GCTATCTTGGCTCAG[C/T]GCAATCTCCGCCTTC | 22992 |
rs541407798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67252954 | TAGCATCACTGGAGG[A/G]CAGTGTAGGGCAGCA | 22992 |
rs541435585 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67214129 | CACCAGAACCTCCAC[A/C]TCCTGGGTTCAAGCG | 22992 |
rs541473739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67241129 | TCAGCAGAGGAAATG[A/G]GCAGAGTCCTACTCT | 22992 |
rs541506362 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67210936 | CACTTGAGCCCAAGA[A/G]TTCGAGACCACTCGG | 22992 |
rs541510776 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67240573 | TGGTTGGCTTTTGAG[A/T]ATCCTTTCCCTCTCT | 22992 |
rs541510882 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67251008 | GCCATTTGCCTCCTG[A/G]CCCTGCTCTATACTT | 22992 |
rs541544249 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67147219 | GCCAGATCTTTTGTG[C/G]CACTCTGGGAATGGT | 22992 |
rs541545098 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67218600 | TAGTATATTTTATTT[A/T]ATTTATTTATTTATT | 22992 |
rs541589167 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67189645 | AGGAGTTCGAGACCA[A/G]CCTGGTCAACATGGC | 22992 |
rs541598534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67250004 | CTCTGGTCCCCTGAG[A/G]GCAAGGGAGGTCCAC | 22992 |
rs541651399 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67208476 | GGAGAGGAATATTAA[A/T]ATTCAACCTTGGGGC | 22992 |
rs541652387 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-3-prime | KDM2A, LOC107984341 | GRCh38.p7 | 11:67117584 | CAGGTTATATGATTC[A/T]CTCCATGCCCTACCT | 22992 |
rs541731205 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67225093 | TTGGCCTCCCAAAGC[G/T]CTGGGATTACAGGTG | 22992 |
rs541755471 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67178570 | CTCTAGCCCCTGGCA[A/C]CTATGAATCTAGTTT | 22992 |
rs541776975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67207115 | GCATCAAATCAGTAT[A/G]GATCAGTAAGTAAGA | 22992 |
rs541789463 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67169248 | CGTGAGCCACTGCAC[C/T]CGGCCTAATCCATGT | 22992 |
rs541790586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67187271 | AGGATATAGAAGTCA[A/G]ATACCAAAATGACAG | 22992 |
rs541793488 | snp | A/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185198 | GAGCTGAAAAGTACA[A/G]TAATTAAAATGAAAA | 22992 |
rs541816287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67216028 | ATGTATACTTAATAT[A/G]CCCTGGAAATGAATC | 22992 |
rs541883133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67177535 | AGGGTCGGGGTCATC[A/G]GTATCACAGAGCGGC | 22992 |
rs541899493 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67231175 | CCAGGCTAAAACTAT[G/T]TTTTAAACATACATG | 22992 |
rs541934307 | in-del | -/ACCCAGGCTGTGCA | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67200711 | CAGTTTGACCCTGTT[-/ACCCAGGCTGTGCA]ACCCAGGCTGGTTTA | 22992 |
rs541948996 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255460 | TCCCAGGGAAGAAAA[C/T]GGCCCTGTCTCCATG | 22992 |
rs541952424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67193651 | AGATCACCTGAGGTC[A/G]GGAGTTCGAGACCAG | 22992 |
rs541985517 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67214455 | GTGATCCACCTGCCT[C/T]GGCCTCCCAAAGTGC | 22992 |
rs542001014 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KDM2A | GRCh38.p7 | 11:67201238 | TGTGTGTGTGTGTAT[A/G]TATATATATTTCATA | 22992 |
rs542016375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67229942 | AGCACTTTGGGAGGC[C/T]GAGGAGGGCCAATCA | 22992 |
rs542017400 | snp | G/T | 0.0119091 | 0.0762411 | downstream-variant-500B | KDM2A | GRCh38.p7 | 11:67258454 | ATGTCCAGCTAATTT[G/T]TGTGTGTGTGTGTGT | 22992 |
rs542019634 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67123722 | ACTCTTGTCACCCAG[G/T]CTGGTGTCCAATGGC | 22992 |
rs542035215 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67251966 | GTGCTGTCTCTCTTC[C/T]CCTGCCAACCAGGCT | 22992 |
rs542054394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67154701 | GCCTTGGCCTCCCAA[A/G]GTGTTGGGATTACAG | 22992 |
rs542058492 | snp | C/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67121043 | CGTCTAGGCCTCCGA[C/T]AGTTGTAATGTGATT | 22992 |
rs542087964 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67191590 | AAGGAGGAAAAAAGT[G/T]ACATGATCATCTCAA | 22992 |
rs542089480 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67145787 | CTTTTGGACCTTTGC[A/G]TATGCTGTTCTTTCT | 22992 |
rs542106073 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67237829 | TTGTGCACCTGTAGT[A/C]CCAGCTACTCAGGAG | 22992 |
rs542120233 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67208466 | TGGATGTAACGGAGA[A/G]GAATATTAAAATTCA | 22992 |
rs542130502 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67189550 | GCAACATAGCAAGAC[C/T]TTATCTCGGCCGGGC | 22992 |
rs542181108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67160638 | TAGCTGGGTGTAGTG[A/G]CGCATACCTATAATC | 22992 |
rs542209641 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67151540 | TTTTTAGTAGAGACC[A/G]GGGTTTCACCATGTT | 22992 |
rs542222096 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67159647 | AACTAGTAAATAATC[C/T]GTGGGGTGATTCTTT | 22992 |
rs542224329 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67146256 | CCTCAGCCTCCCAAA[A/G]TGCTGGGATTACAGG | 22992 |
rs542249330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67124375 | GGAGTGCAGTGGCAC[A/G]ATCTTGGCTCACTGC | 22992 |
rs542266097 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67151874 | CTCAACCTCCTGCGT[A/T]GCTAGGACTATAGGC | 22992 |
rs542290604 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67205628 | GTATTTTTTTGTTTT[G/T]TGTGTGTGTATGTTT | 22992 |
rs542300087 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67216959 | CAAAAAAACATGAGG[A/T]CTTGTCCGGGCACAG | 22992 |
rs542348103 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67131318 | GACAAGAGCGAAACT[A/C]CGTCTCAAAAAAATA | 22992 |
rs542409651 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | KDM2A | GRCh38.p7 | 11:67139269 | TTTTCTTTTGAGACG[C/G]AGTCTCGCTTTGTCC | 22992 |
rs542433222 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KDM2A | GRCh38.p7 | 11:67228700 | CGAAAAAAAAAAAAA[A/G]AAAGAAAGAAAGAAC | 22992 |
rs542434440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67165985 | CATGTATTATACTGA[C/T]GACTTAACAGTTGCA | 22992 |
rs542461011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67129501 | GCACTTTGGAAGGCC[A/G]AGGCGGGCGGATCAC | 22992 |
rs542513450 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67174231 | CCACTGCACTCCAGC[C/T]TGGGCGACAGAGTAA | 22992 |
rs542517111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67199816 | ACAGATTTTCCATGT[A/G]AATGAAACAGCCTTC | 22992 |
rs542517233 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67204261 | TACCAGTGTCATCAA[C/G]TTTTTTCACAGTGTG | 22992 |
rs542520259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67137568 | GTAAAGGAGGTAAAT[A/G]TAAGTATGACTCCCA | 22992 |
rs542525960 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67247797 | GTGCATATTACATCT[A/T]TTAACATATCTCAAA | 22992 |
rs542564676 | in-del | -/TT | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67220317 | GCATCCCACAGTATC[-/TT]GGATTTTTATAAGGC | 22992 |
rs542599303 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206292 | AAAAATTAGGCAGGC[C/G]TGGTGGCACACGGCC | 22992 |
rs542605723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67182241 | CTTCCTTCCCCTAAA[A/G]GGAGTAGAGAAATTT | 22992 |
rs542615003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67245083 | AGTGGGCAGATCTGG[C/T]CATAGTGGGCCAAGC | 22992 |
rs542635268 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67155092 | CCATCTTGGCTCACT[A/G]CAACCTCTGCCTCCC | 22992 |
rs542641801 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67135509 | GCCTCATGAGCTGGT[G/T]GTGGCCCTCAGCCTT | 22992 |
rs542643788 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67143878 | TTCAAGTGATCCGCC[C/T]GCGTCGGCCTCCCAA | 22992 |
rs542653531 | snp | C/T | 0.00113369 | 0.0237815 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255508 | TCCAGTGCGCGTCTC[C/T]CCTCCATCACACTCT | 22992 |
rs542674237 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67136604 | ATTCCTTGAGATTGA[A/C/G]TGATCAGTGAAAGGC | 22992 |
rs542706742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67143280 | CCAAGGTGTTGGGAT[C/T]ACAGCCGTGAGCCAC | 22992 |
rs542742114 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67173448 | TTTTTAGTAGAGAAG[A/G]GGTTTTGCAATATTG | 22992 |
rs542761736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67214159 | GATTCTCCTGCCTCA[A/G]CCTCCCAAGTAGCTG | 22992 |
rs542786567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67253851 | TGGGGCCCAGAGAGT[A/G]TAAGCCTGAAAAAGT | 22992 |
rs542800381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67221667 | CATTTCTTTTTATTT[A/G]TTAAGAGTAACAAAA | 22992 |
rs542822607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67149674 | AGATGAAGAATAGAA[A/G]AGATAGTAATCTAAT | 22992 |
rs542827617 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67146358 | GATTGTCTTTTTACT[C/T]ACTTTTTATAGATCC | 22992 |
rs542827991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67175161 | ATCCAGGGTTACTGT[A/G]AGGATTGAATGTTTT | 22992 |
rs542886306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67221112 | GTTGTTTGCTGGCTA[A/G]CCTCCACCTTAGAGA | 22992 |
rs542887291 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KDM2A | GRCh38.p7 | 11:67236593 | TTGTTGAATACTTTT[C/T]GACTTTCCTGTTTTC | 22992 |
rs542923114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67228429 | GGACACGCTGGTTCA[C/T]GCCTGTAATCCTAGC | 22992 |
rs542968441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67218823 | ACCATGTTGGCCAGG[C/T]TGGTCTTGAACTCCT | 22992 |
rs542990578 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67240736 | CCAAACCCCCTCTAG[C/T]GAAGGGTGGTGGCTT | 22992 |
rs542995624 | in-del | -/A | 0.0535932 | 0.154675 | intron-variant | KDM2A | GRCh38.p7 | 11:67140366 | GTGAGATCTTGTCTC[-/A]AAAAAAAAATATCAT | 22992 |
rs543029555 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67189799 | GAGCCAAGATCGCAC[A/C]TTGCACTCCAGCCGG | 22992 |
rs543033045 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67120563 | GCAATCGTTTATTTT[A/T]TTACTTTATCCAAAA | 22992 |
rs543061139 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67217183 | GGAGGTGGAGGTTAC[A/G]GTGAGCCAAGATTGT | 22992 |
rs543066527 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67236594 | TGTTGAATACTTTTC[G/T]ACTTTCCTGTTTTCT | 22992 |
rs543093582 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67244501 | CGGTACATGGCACTT[C/G]ATACAGAAAGCTCAG | 22992 |
rs543094429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67127362 | ACTCCCAGACTCAAG[C/T]GATCCACCTTGGCTT | 22992 |
rs543117344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67197814 | GTTGACCCTTGAACA[A/G]TGCAACGGCTAGAGG | 22992 |
rs543131700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67234166 | ATCTCAGAAAAGATA[C/T]AGCAAGCTTAGAGCT | 22992 |
rs543200430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67188045 | AAAAAAAATAATAAT[A/G]GTAATTTTAAAAGTT | 22992 |
rs543215159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67243166 | ACCATTCTGGGGAAA[A/G]CAAGAACAACTAGAG | 22992 |
rs543322368 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67211341 | AAAATAAGCCAGGTG[C/T]GGTAGCTCACGCCTA | 22992 |
rs543324502 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67121165 | CTTACCTTAAATACT[C/T]CTTTCCGTGAACAGA | 22992 |
rs543331594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67147813 | CTTCCAAGTAGCTGC[A/G]ATTACAGGCGCCTGC | 22992 |
rs543345694 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67173595 | CAGGTTTTGCCATGA[A/G]CCAGGCTGGTCTTGA | 22992 |
rs543377180 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67163726 | CTGGGCGTGGTGGTG[A/C]GTACCTGTAATCCCA | 22992 |
rs543421281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67156078 | AATGTGGAGAAACCC[C/T]GTCTCTACTAAAAAT | 22992 |
rs543480134 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67217611 | CAAGTTCTATAGGCT[G/T]GGAAAATTGCTTGCC | 22992 |
rs543495825 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67225215 | ACTGACTTTGAAAAC[-/A]AAAAGATATCATTCT | 22992 |
rs543503445 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67161949 | GATGCTTTTTCAGAG[A/C]TTCAACTCAGTTTTC | 22992 |
rs543512565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67126740 | AAGTATTTTTTGCCA[A/G]GCTTCATTATTTACC | 22992 |
rs543551949 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67134636 | CAGCCTCCTGAGTAG[C/T]TGGGATTACAGGTAT | 22992 |
rs543553079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67179473 | AGACATGGTTTCTCC[A/G]TGTTGGTCAGGCTGG | 22992 |
rs543595781 | snp | G/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67205904 | CATCTCTTGTTAGAA[G/T]TCTACTTATTCTTCT | 22992 |
rs543606155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67242166 | CACTGTAGCATTGTT[C/T]GTAAGTCATTTAAAT | 22992 |
rs543611455 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67133952 | CCACCTCGGCCTCCC[A/C]AAGTGCTAGGATTAG | 22992 |
rs543641844 | snp | A/G | 1.69717e-05 | 0.002913 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67252832 | CTCTAAAAAGCAACT[A/G]ACATGGCTCGTCAAT | 22992 |
rs543669861 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67178530 | ACCCATACTATTAAC[A/G]GTCACTTCTCCCATT | 22992 |
rs543705199 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67133065 | GCCTTGAGTTTTAGT[A/C]TCAAGTCTCTTACCA | 22992 |
rs543740066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67240988 | ACAAAAATCTTGCAG[A/G]TAGAATTAGACTGCT | 22992 |
rs543747021 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67218370 | ACCTGCTAGATACTA[C/T]GCTTAGAGCAAATAT | 22992 |
rs543768198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67147333 | CAGTCATGAGGTCAG[A/G]AGATTGAGACCATCC | 22992 |
rs543825814 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67133391 | ATAGGTGTGAGCCAC[C/T]GTGCCTGGCCTATTT | 22992 |
rs543826614 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67208675 | ACTCGGGAGGCTGAG[G/T]CATGAGAATCGCTTG | 22992 |
rs543838576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67139487 | TGACCTCTGGTGATT[C/T]GCCCACCTCGGCCCC | 22992 |
rs543845867 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67146408 | AGTCTTATTTATCAG[A/C]GCATTGACAGTGTTT | 22992 |
rs543866281 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67167089 | CCTCAAAAAAAAATT[-/A]AAAAGTTTAATATTG | 22992 |
rs543876410 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67170302 | ACAATAATATAGCTA[A/G]AAATGTAGTGTCCCT | 22992 |
rs543876838 | in-del | -/AC | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67168491 | TTTTAATTTTTGTAT[-/AC]AGAGTGTCTGGCTAT | 22992 |
rs543892279 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67201202 | CTGTCTCAAAAAAAA[A/G]AATATATATATATAT | 22992 |
rs543893851 | snp | A/G | 0.00636936 | 0.0560724 | downstream-variant-500B | KDM2A | GRCh38.p7 | 11:67258315 | TTGAGATGGAGTCTC[A/G]CTCTGTCGCCCAGGC | 22992 |
rs543929919 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67257225 | CAATGGTTTCTTTTG[A/G]GTTTTGGTTTTTATG | 22992 |
rs543958778 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-3-prime | KDM2A, LOC107984341 | GRCh38.p7 | 11:67117394 | CAAAGCAGAGAATGT[C/T]TGTACAAACTCCCCA | 22992 |
rs543959947 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67249170 | CAAGGATTTTTGAAG[G/T]TGACTAGGGCCAAAG | 22992 |
rs543972305 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67207812 | GGCAGATCGCTTGAG[C/G]TGAGGAGTTTGAGAG | 22992 |
rs543977819 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67134547 | AGTCAATCTGTTGCC[A/G]AGGCTGGAATGTAGT | 22992 |
rs543985491 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67225028 | TTCTAGTAGAGACGG[A/G]GTTTCAGCAGGCTGG | 22992 |
rs544068616 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | KDM2A | GRCh38.p7 | 11:67232698 | TTTTTTTTTTTTTTT[A/T]AATTTTAATTAATTA | 22992 |
rs544072647 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67224352 | GTTCATGCCTATAAT[C/G]CCAAGTACTTTTTGG | 22992 |
rs544104447 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67132426 | GTAGCTGGGATTACA[G/T]GCACGTGCCACCACG | 22992 |
rs544109199 | snp | A/G | 0.000547007 | 0.0165289 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67231585 | GGAGTTAAATGGGTT[A/G]GAGTCTGGGAATGGG | 22992 |
rs544143044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185820 | TTCTCTCATTCTCTT[A/G]CTGTCTCGCTTTTCA | 22992 |
rs544150186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67223019 | GCAACATGAAGAAAC[C/T]CTGTCTCTACTAAAA | 22992 |
rs544156942 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67170172 | AAACACCTTGTGATA[A/G]AAAATGCTGATTAGA | 22992 |
rs544196975 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67121862 | TGTTGGGATTGATTG[-/A]AAGACAAGTAGGTAG | 22992 |
rs544197395 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67249964 | TCTGAGGGAATGACC[C/T]CCTCTCCAACGTGAC | 22992 |
rs544237591 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67229887 | AAAGAAAAAAAAAAA[A/T]ACATCTAGGCCGGGT | 22992 |
rs544237602 | in-del | -/AG | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67130200 | AGTTTGCAAAACCCA[-/AG]AGAGAGCAGTTTTCT | 22992 |
rs544297144 | in-del | -/CAGAACC | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67195104 | CAGCTCATTTCTTGT[-/CAGAACC]CAGAACCCATTGAGA | 22992 |
rs544298849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67192823 | TTTGAGAGTTTAGAC[A/G]GTATAAGCCTAGAAG | 22992 |
rs544298910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67201172 | GCACTACAGCCTGGG[C/T]GACTGAGCAAGACTC | 22992 |
rs544335560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67200603 | TGCAGGCTCAGTGTC[C/T]CTGGGCTCAGGTGAT | 22992 |
rs544391635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67129788 | TAGTGGCACATGCCT[A/G]TAATCCCAGCTACCC | 22992 |
rs544401528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67160501 | TTCTGGGCCGGGTGC[A/G]ATGTTCACACCTGTA | 22992 |
rs544420214 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67183401 | GATGACCTGCATCAG[A/C]ATTGCTTGTGATATT | 22992 |
rs544453352 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67137876 | GATCTCGGCTCACTG[A/C]AACCTCTGCCTCCCA | 22992 |
rs544455809 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67190815 | ATAACCTAGATGAAG[C/T]GTACAAATTTCTAGA | 22992 |
rs544467303 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67198922 | TAGCTGAGATTACTG[A/G]CATGCACCACCATGC | 22992 |
rs544481978 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67193680 | AGCCTGACCAACATG[A/G]CAAAACGCCGTATCT | 22992 |
rs544484318 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67246726 | CTTCTTAGAAAGTAT[C/G]AGCTAAAATCATGAC | 22992 |
rs544544475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67176995 | GGGCACGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 22992 |
rs544604403 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67205167 | TTTTGCTAGCACTCA[G/T]TATTTTCCATTTTTT | 22992 |
rs544606203 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67166361 | GGCTAATTTTCACAT[G/T]TTTTAGTAGAGACAG | 22992 |
rs544612635 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67172969 | GGAATATTTATAGAC[A/G]TAATGTGATGCACTG | 22992 |
rs544615414 | in-del | -/A | 0.0611083 | 0.163768 | intron-variant | KDM2A | GRCh38.p7 | 11:67217241 | GAGTGAAACTCTGTC[-/A]AAAAAAAAAAAAAAA | 22992 |
rs544634460 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KDM2A | GRCh38.p7 | 11:67176237 | GGTATGTAATAGTCA[A/G]GTTTATTTCTTTCAT | 22992 |
rs544646193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67184007 | CCAGCTACGTGGGGG[A/G]CAATTCCTTGAGCCC | 22992 |
rs544670676 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67163151 | ATAACTTCATTGCTA[C/T]TCTGTCTTCTAGCGC | 22992 |
rs544673003 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67237349 | AGTTGATAATTTGGG[C/G]GTTATTCTGACACTA | 22992 |
rs544703187 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67213424 | TAGTGTAAAATGTTG[C/T]GTATTGCTTTCACTT | 22992 |
rs544728380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67138452 | TGTTTTCAAAGTGTG[C/T]TCCCCAGACCACATT | 22992 |
rs544732092 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67191527 | TTTATTCCTGGAATA[C/G]ATGATTTGACATGTG | 22992 |
rs544734928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67174078 | GCCTGGTCAGCATGT[C/T]GAAACCTTGTCTCTT | 22992 |
rs544760297 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67160141 | GTCTATTAGGACTAA[C/T]TGGGAGAAAAACTCT | 22992 |
rs544761074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67247720 | GTGAGCCACCATGCC[C/T]GGCCAACTTTACAAT | 22992 |
rs544769848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67165882 | TACGGTCAACTTTTA[A/G]GGGTTTTTTCTTTTT | 22992 |
rs544792102 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KDM2A | GRCh38.p7 | 11:67145313 | AACATGGTGAAACCC[C/T]GTCTACAAAAAACAC | 22992 |
rs544793101 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67157637 | GAAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAC | 22992 |
rs544795993 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67205243 | TTTTGATTTGACATT[C/G]ACTTTTTCTTTTAAA | 22992 |
rs544823937 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255758 | TTGCACTTATTGGGG[C/T]TGAAGCTCTTCAGAG | 22992 |
rs544832352 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67186780 | TACATTTAAAATAAT[C/T]AGTAGAACGGGGTAT | 22992 |
rs544853903 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67181483 | GTGGTATTGATAACC[C/T]AAAACAATAGTAATT | 22992 |
rs544912965 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67227389 | TCTTTGTTCCATGGC[C/T]TTCTGATTCAGGGGC | 22992 |
rs544921887 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67128071 | CCAGGCCGGAGTGCA[A/G]TGGCACTACCACTGC | 22992 |
rs544935826 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67235996 | TAGGACATGTAACAG[A/T]ATGTATAGTACCATC | 22992 |
rs544959084 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67142312 | AAAGTGCTGGGATTA[C/T]AGGCATGAGCCACCG | 22992 |
rs544975820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67143221 | GAGACGGGGTTGGCT[A/G]GTCTTGAACTCGTGA | 22992 |
rs544981972 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67127479 | CCTAGCAAAAAAAAA[A/T]AAAAAATAAGAAATT | 22992 |
rs544986744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67150728 | TGGGAGAGAGGGTCA[A/G]CAGACAAGGTGAAAG | 22992 |
rs544987169 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67135353 | ACAAGCGTGAGCCAC[C/G/T]GCGCCCAGCACAGAT | 22992 |
rs545024052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67221465 | ATATATTATAGGAAT[A/G]GTCACTGACCTATGT | 22992 |
rs545038789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67149390 | CAGTGAGCTTTCAAT[A/G]AAAGGTATCTGTTGT | 22992 |
rs545076431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67148756 | CAGTGAGCTGAGATC[A/G]TGCCATTGCACTCCT | 22992 |
rs545146968 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67122024 | TGCTTTCCTCGTAAG[G/T]TTTCCCTATTGGAGT | 22992 |
rs545174402 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | KDM2A | GRCh38.p7 | 11:67128694 | TATTATTTTCTGTTG[C/T]TTTATTTTGCTGAGC | 22992 |
rs545175789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67228296 | AGTACCAAATTCATC[A/G]CTGGAATTGAATACC | 22992 |
rs545208516 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67121454 | AATCTGTGATTAAAA[C/G]TTTTCGGGTGACTTT | 22992 |
rs545211460 | snp | A/G | | | utr-variant-5-prime, intron-variant | KDM2A | GRCh38.p7 | 11:67240139 | TGAAGGGCTCGAGAA[A/G]GAGCCCAGAGCGCTG | 22992 |
rs545213071 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67147180 | AGAATAGAAATACGC[A/C]TGTTTGTATTTCATC | 22992 |
rs545236423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67120306 | GAGGGCTCTGCCTCT[A/G]ACTGCTCTGCAAACT | 22992 |
rs545237416 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KDM2A | GRCh38.p7 | 11:67156972 | TGTGGTAGAGGCTGT[A/G]TGGCCCACAAAATTT | 22992 |
rs545239945 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67189771 | CTTGAACCTGGGAAG[C/T]GGAGGTTGCAGTGAG | 22992 |
rs545266576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67244918 | GGGAACCCGGGAGGC[A/G]GAGCTTGCAGTGAGC | 22992 |
rs545299614 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67119301 | AATGGCGGCGGCTGC[C/T]TCAGCGGCTCCTCCT | 22992 |
rs545299615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67127248 | AGGCATGCATGTGCC[A/G]CCATGCCTGGCTAAT | 22992 |
rs545300384 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67235152 | TCCATCTCAAAAAAA[A/C]AAAAAAAAGAAAAAA | 22992 |
rs545353639 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67233971 | GTGAGATGACTACAC[A/C]GGCCGACAGTGTTTG | 22992 |
rs545446987 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67196242 | CCATGAGCCTCAGAT[G/T]CAGGCTACCACTGCT | 22992 |
rs545459363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67157441 | GCAAAAAAATTCCTG[A/G]TTTCTCTTATTAACA | 22992 |
rs545459973 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67235246 | TGGGAGGGGTTGTGG[C/G]TAATGTTGACTCTTG | 22992 |
rs545477032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67242097 | AAATTAAAAAAAATA[C/T]ATTTGTTTCAAAATA | 22992 |
rs545477637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67253085 | GACAGCAAAGAGAAC[A/G]GAATCAGTGTTGCTG | 22992 |
rs545482853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67204008 | GTTTCACCATGTTGG[C/T]CAGGCTGGTCTCAAA | 22992 |
rs545504045 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67227964 | TTCCTGGGTTAATGA[C/T]TACAGTAATTCCATT | 22992 |
rs545508144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67133804 | CCTCCCAGGTTCAAG[C/T]GATTCTCCTGCCTCA | 22992 |
rs545519519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67203275 | ACAGTATAATGTAAA[C/T]ATATGCACTGTGAAA | 22992 |
rs545536660 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67187552 | TATTTAATTGATTTT[A/T]TTTATTTATTTATTT | 22992 |
rs545558295 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67225436 | AGTTCAGGAGTTCGA[A/G]ACCAACCTGGCCAAC | 22992 |
rs545569365 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67141284 | ATAGATTGTAATGAC[C/G]AAGTCAGAGTATTTG | 22992 |
rs545572007 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67202420 | ATTGCATGCTACAGA[G/T]AAGTCTCTTTGTGAA | 22992 |
rs545602529 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67180061 | ATGATTTCATCAGTA[C/T]GTTCCTTTCTTTCCT | 22992 |
rs545615838 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67211030 | CCACTACACTCCAGC[C/G]TGGGTGACAGAATGA | 22992 |
rs545621795 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67163649 | ATGAATGAGGTCAAG[A/T]GATCGAGATCATCCT | 22992 |
rs545622556 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67195262 | TAGTCCCAGCTACCC[A/G]AGAGGCTAAGGCAGG | 22992 |
rs545651165 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67251872 | TAAATTCTCCTTAAT[A/C]TTTCTCTGTCTAGGG | 22992 |
rs545702756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67208623 | TAAAAATACAAAAAT[C/T]AGCCAAGCATGGTTG | 22992 |
rs545707696 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67161166 | TAGGAGTTTGAGACT[A/C]ACTTGAGAACGCAGT | 22992 |
rs545711972 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67231372 | GGTGTCCTCCTAGGT[C/G]AGGATCCTGTTTCTA | 22992 |
rs545744546 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67193756 | CTCCCAACTACTTGG[G/T]AGGCTGAGGCAGAAG | 22992 |
rs545799075 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67188162 | GTAGTCCAGCCTGGG[A/T]GACAGAGCCAAGACC | 22992 |
rs545799963 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67214506 | ACTGCACTGGGCCTA[A/G]TTTTGTATTTTTAGT | 22992 |
rs545883588 | snp | A/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185506 | TGGTGGTGGGCCCCT[A/G]TAATCCCAGCTACTT | 22992 |
rs545952991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67140758 | ACTTTGTCTCAAAAA[A/G]AAAAAGTTACAAGTA | 22992 |
rs545995362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67147674 | GAGTAGTTCCCTTTC[A/G]TTAGAGATTCTTTTT | 22992 |
rs546004352 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67217111 | GCTGGGTGTGGTGGC[A/G]CACGCCTGTAGTCCC | 22992 |
rs546045107 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67184776 | AGGCTCAGAGAAGAC[A/G]TAAGAAAACTTAAGT | 22992 |
rs546045954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67132352 | GCAATGGCACGATCT[C/T]GGCTCACTGTAACCT | 22992 |
rs546058668 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67147268 | TTCCACTGGGCCGGG[G/T]GCGGTGGCTCAAGCC | 22992 |
rs546096813 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67155412 | CTCCTAGGCTCAAGC[A/G]ATTATCCTGTCTCAG | 22992 |
rs546134142 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67193276 | ATTACAGGCGTGAGC[C/T]ACCGCACCTGGCCGA | 22992 |
rs546163068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67249884 | CACCTATAATTCCAG[C/T]ACTTTGGGAGGCCAA | 22992 |
rs546181802 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67161238 | AAAACAAAAGAAAAA[C/G]AAGACTTTAGTGATG | 22992 |
rs546182320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67154803 | TGTCTGGCTTTCACT[C/T]AGCATATGTTCGAGG | 22992 |
rs546244060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67229642 | TTGGGAGGCTGAGGC[A/G]GGCGGATCATGAGGT | 22992 |
rs546258631 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67170702 | ACAGGTGTGAGCCAC[C/T]GCACCTGGCCCAAGC | 22992 |
rs546303774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67224275 | ATTCAAAACAGTATC[A/G]TTTGGCTTATCCTTT | 22992 |
rs546321114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67125331 | GACTACAGCCCTGTG[C/T]CACCATGCCTGGTTA | 22992 |
rs546351670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67152034 | TAAAATTAATTTCCC[A/G]CCGGGTGCAGTGGCT | 22992 |
rs546380668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67231440 | TGGAATAAAGATAGA[C/T]CATTTTTTTAAATGT | 22992 |
rs546384445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67124502 | TATTTTTAGTTGAGA[C/T]GGGGTTTCGCTATAT | 22992 |
rs546390397 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67158957 | GCGCATTTCTCCCAG[G/T]GAGTGGCTTGTCTTT | 22992 |
rs546390490 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | KDM2A | GRCh38.p7 | 11:67151266 | ACGCTATGGTAGCCA[C/T]TAGCCACAGGTTGCT | 22992 |
rs546399208 | in-del | -/TAGAT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67234114 | TCACTTAAGATCAAA[-/TAGAT]TAATTATTCCTATAT | 22992 |
rs546463591 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67139401 | AGGCACCCACCACCA[C/T]GCCCAGCACATTTTT | 22992 |
rs546468321 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67230658 | ACATAAAAAAAAAAA[A/C]CCCACATAATAATCA | 22992 |
rs546478157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67158166 | TGTAGTTTTGCCCTT[C/T]CTAAAATGTCGTATA | 22992 |
rs546516671 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67192691 | CTCAAGTGATCCATC[C/T]GCCTTGGCCTCCCAA | 22992 |
rs546553658 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67122227 | ATTTATGGTGGTTTT[A/T]TTTGGCTCTGCATTT | 22992 |
rs546591112 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67238131 | TTCTTGTATTATGTA[A/G]TGTCATGGTCTTAGT | 22992 |
rs546610707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67138101 | GCGCCTGGCCAAACT[A/G]TAGTATTATTATAGG | 22992 |
rs546614970 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67128926 | GATTAAGCCACTAGA[A/G]TGGAGGAGGGTCTGG | 22992 |
rs546615346 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67121586 | TATATGTAGCCTTTA[G/T]CTTTTATAGAAACCA | 22992 |
rs546635120 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67194312 | CCCCAGCTGTCCCAG[C/T]AGCTGCTCAGCCAGA | 22992 |
rs546674600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67236059 | GTGCATTGCAGAGGA[A/G]TCTAAAAGGGTACAT | 22992 |
rs546676184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67199138 | CCATGAACTGTATCC[A/G]TATAGGAGAGCAGAC | 22992 |
rs546680828 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67159004 | GTCTTTCACAGAGCA[C/G]AAGTTTTCAGTTTCA | 22992 |
rs546691624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67165206 | GGCTCACCGCATCCT[C/T]CACCTTCTGGGTTCA | 22992 |
rs546704728 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255570 | AGGAGTCCCAGACCC[A/G]TGCCGATCACACTGG | 22992 |
rs546709772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67247168 | GACCTCGTCTCACTG[C/T]AACCTTTGTCTCTGG | 22992 |
rs546725399 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67155411 | ACTCCTAGGCTCAAG[C/T]GATTATCCTGTCTCA | 22992 |
rs546728743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67173635 | CCAAAGTCATCTGCC[C/T]GCCCTGGCCTCCCAG | 22992 |
rs546763343 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67227826 | TCCACCCGTCTGGGC[C/G]TCCCAAGTACCCTTT | 22992 |
rs546763842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67235461 | AGGCATGCACCACCA[C/T]CCTGGCTAATTTTGT | 22992 |
rs546775663 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67122480 | TGTAGGCATGTGCCA[C/T]CACGTCCAGCTAATT | 22992 |
rs546807238 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67205682 | AGACGGTGTTTTGCT[A/G]TGTTACCCAGGCTGG | 22992 |
rs546812907 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67152651 | TACCGGAAAAATTTA[A/T]ATTACATATGTAGCT | 22992 |
rs546851810 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67182902 | TAAATTTTCTTCCTA[A/G]CACTAGAATTTCTAT | 22992 |
rs546852011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67214344 | CGAGTAGCTGGGACT[A/G]CGGGCGCCCGCCACC | 22992 |
rs546891982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67134924 | TTGAATTTTCACAAA[A/G]CTAACTTCATGGTCA | 22992 |
rs546895939 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67138563 | AGGTGGGCAGATCAG[C/T]AGAGGTCAGGAGTTC | 22992 |
rs546937348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67179500 | CTGGTCTCTAATCTC[A/G]AACTCCCGACCTCAG | 22992 |
rs546953348 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67142602 | TGGGGTTGGGGGGGC[A/G]TCAAGGCAAGAGAAT | 22992 |
rs546987419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67174529 | TACCTACTTGCATCT[A/G]GTGTTGCTTCCTCAT | 22992 |
rs547003225 | in-del | -/C | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67225271 | TGGTATTTCTACTTA[-/C]AAAATATAGTTATTC | 22992 |
rs547027121 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67217918 | TGGGTTATTTAGCCA[-/T]TTTTTTTCCTTAATG | 22992 |
rs547068085 | snp | A/T | 0.0498117 | 0.149749 | intron-variant | KDM2A | GRCh38.p7 | 11:67203470 | ATTTATTAATTATTA[A/T]TAATTATTAATATAT | 22992 |
rs547107231 | snp | A/G | | | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67120024 | TTACTTCTCACTTGG[A/G]CAAGAACTCAAGAGC | 22992 |
rs547110367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67218991 | TTGGACACCCCTGAA[C/T]TGTAAACTATCTTGT | 22992 |
rs547112420 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67210503 | CCTGAATTTATTCAC[C/T]CTGTCCCTAGTTTTA | 22992 |
rs547121575 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67135688 | TTTGCAAAGTACTTC[G/T]TTGTCTCTTGTGTCT | 22992 |
rs547158790 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67181568 | GTGTTTCATATTAGA[C/G]GTAAATGAGAAAATA | 22992 |
rs547185034 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67143382 | CATCGGTATGAAATA[A/G]TGTTGGTTCAGTTTC | 22992 |
rs547225440 | snp | C/G | | | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67119810 | GCGGGGGCGCCCCGG[C/G]CTCGGCGCCGAGGGG | 22992 |
rs547237645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67197276 | CTTCCTGGGCTCAAG[C/T]GATCCTCCCACCTCA | 22992 |
rs547238122 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67119753 | GCGGCCGGGGCCGGC[C/G]CGGGGCTCGGGCCCG | 22992 |
rs547239561 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67167001 | GAGAATCACTTGAAC[C/T]TGGGAGACGGAGGTT | 22992 |
rs547267812 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67254022 | AGAAAGAAAACTTGT[C/T]TGGTTTCCTAGAAAC | 22992 |
rs547281704 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67188354 | GGGTGTGGTGGCAGG[C/T]GCCTGTAGTCCCAGC | 22992 |
rs547311317 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67149789 | GCGATGATACGATCT[C/T]GGCTCACTGCAACCT | 22992 |
rs547324248 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67226007 | GAGGTGGAGGTTGCA[A/G]TGAGCCAAGATTGCA | 22992 |
rs547329923 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67187730 | AGGTGCCCGCCACCA[C/T]GCCCGGCTAAATTTT | 22992 |
rs547346692 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67221663 | AGTACATTTCTTTTT[A/T]TTTGTTAAGAGTAAC | 22992 |
rs547364865 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67186971 | TAATAACTAATAGGG[C/G]CACAGTATATAAGGA | 22992 |
rs547379878 | in-del | -/TA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67196866 | TAAGATAGAACATTT[-/TA]TGTTTTTTGTATTTT | 22992 |
rs547430565 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67163841 | AGCCTGGTGACAGAG[C/T]GACACTCCATCTTAA | 22992 |
rs547440863 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67253714 | CAGATATGACGCTGT[A/G]GAAGAATAGAAGAGC | 22992 |
rs547488989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67194002 | CGTAATCTCACTGCA[C/T]CTGTCCACCATTTTA | 22992 |
rs547503682 | in-del | -/TTTGTTTTGT | 0.0346009 | 0.126898 | intron-variant | KDM2A | GRCh38.p7 | 11:67198769 | AGTAGTTTGTTTTGT[-/TTTGTTTTGT]TTTGTTTTGTTTTGT | 22992 |
rs547504180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67156617 | CCAGCTACTCAGGAG[A/G]CTGAGGCAGGAGAAT | 22992 |
rs547526909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67226796 | ATTAAATGAGCACTG[A/G]CCGCGAGCTGCTCTT | 22992 |
rs547542686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67194651 | AAATAGAGGGCTCTC[A/G]GTGCTGCTTACCTGC | 22992 |
rs547572876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67147397 | AATAAAGAAAATTAG[C/T]CGGGTGTGGTGGCGG | 22992 |
rs547580820 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67202115 | TGCAAATGTGGTGAA[A/G]ATAGTGAGAGAGCTA | 22992 |
rs547603572 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67244646 | CTTTAGGTTTTGTAC[A/G]CCACACAGTCAACAA | 22992 |
rs547609811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67161988 | TATTATGCTCTTAGT[A/G]GTTGTCTTTGGTTAT | 22992 |
rs547638781 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67126780 | TGGAAAAGAAATGCA[C/G]CTTTGAAGATGGTGT | 22992 |
rs547645260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67161430 | TTAGACAGTAGATTA[A/G]GAAAATTAGTATGTT | 22992 |
rs547703295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67133987 | GTGAGCCACCATGCC[C/T]GGCACCAACTGTGGT | 22992 |
rs547732094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67160913 | AGGAGTTCAAGTCCA[A/G]TGTGAGAAACAGCCA | 22992 |
rs547743407 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67237974 | ATTTATACAAATAAA[A/G]CTTTATTTGCAATAT | 22992 |
rs547747901 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67144225 | ATTACTGGGGTGAGC[C/T]ATTGTACCTGGCCCT | 22992 |
rs547750852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67195500 | TTTATGCCATGGGAC[C/T]GTGTTCTAAACTGTC | 22992 |
rs547752508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67125444 | CCTTGGCCTCCCAAC[A/G]AGTCATTTTTTGGGG | 22992 |
rs547766425 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67133274 | TGCGCTAATTTTGTG[G/T]TTTTTTTTGTAGAGA | 22992 |
rs547810480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67132657 | CTCCAGTTTCAGGTC[A/G]GGGTGGTCTAGAAAG | 22992 |
rs547819986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67252184 | AGCCTCTTTTGACCT[A/G]ATACAGTAATGGGCT | 22992 |
rs547823219 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67169444 | AAATGCAGTGGCACC[A/T]TCTCGGCTCACTGCA | 22992 |
rs547832433 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67174387 | TGATTTCCCAACTCT[C/T]ACCTGCTTTTTTACT | 22992 |
rs547835649 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67140550 | TGAGGTCAGGAGTTT[A/G]AGACCAGCCTGGCCA | 22992 |
rs547845601 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67140296 | ACTTGAGCCTGGAAG[A/G]TCAAGGCTGCAGTGA | 22992 |
rs547872756 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67171674 | AATAAATCCATCATT[C/T]GTCTTAATTCTCACA | 22992 |
rs547873376 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67131855 | GAACTTATTGCACTT[G/T]ATCTGTTAAAACGGC | 22992 |
rs547874002 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67179973 | GCAAGGAAAATAGCA[A/C]CTGAGTTTGAAAGTA | 22992 |
rs547878162 | in-del | -/G | 0.00119737 | 0.0244387 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67119698 | TCCCGCAGGCGACCA[-/G]CCCCTGCTGGCCGAG | 22992 |
rs547919348 | snp | C/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206763 | TAAACAAACTTAGGT[C/G]TCTTTGACTCCAAAG | 22992 |
rs547922561 | snp | C/T | 0.000166431 | 0.00912073 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67231740 | CAAGTCTGAAGAAAA[C/T]TTTGGCTGGGGACTC | 22992 |
rs547932664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67130994 | CAAACTCCCAGGTTT[C/T]TTCTCTCATACCATC | 22992 |
rs547951600 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67243306 | CAGAACTATCAAACT[C/G]GGAGGCCTCCCTCCA | 22992 |
rs547957447 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67239541 | GGTGAAGCAGGCAGT[G/T]TGCCGGAGAGAGAAG | 22992 |
rs547961352 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67201558 | GGCAGATCACAAGTC[A/G]GGGGTACAAGACCAG | 22992 |
rs547993238 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67249399 | AGGAGCAGAGAACAG[C/G]GTTGTTGCTTAGAGA | 22992 |
rs548002486 | in-del | -/TG | | | downstream-variant-500B | KDM2A | GRCh38.p7 | 11:67258452 | CATGTCCAGCTAATT[-/TG]TGTGTGTGTGTGTGT | 22992 |
rs548042226 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67217218 | CTGCACTCCAGCCTG[G/T]ACTACAAGAGTGAAA | 22992 |
rs548044168 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67208217 | TAATAAATTTTAAAA[A/T]TTTAAAATTTATTAT | 22992 |
rs548074852 | snp | A/G | 2.92564e-05 | 0.00382457 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67248337 | CTGGGAATGTCCAAA[A/G]TGCTACCAGGAGGAC | 22992 |
rs548090234 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67238299 | GGCCTCTAGAATTTG[C/T]ACTTGCTGCAACTTG | 22992 |
rs548098678 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67145980 | CTGTTCTTCCCGTTT[C/T]TTGTTTTGTTTTTTT | 22992 |
rs548111492 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67130535 | AAGTTGCAAGTGATG[A/T]TGTTTGTGTTATTCT | 22992 |
rs548111898 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67256603 | TCAGGCTTTCCTCTT[C/T]CTGAAGCCCTACAGA | 22992 |
rs548131323 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67216695 | GGAGGCCAAGGCGGG[C/T]GGATCAGCTGAGGTC | 22992 |
rs548154191 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67168464 | GCAATCTTCTTGAGT[A/G]CTAGGACTACATTTT | 22992 |
rs548163418 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67189371 | GCCTACCAAAACTTA[C/T]AGGGATCAGTGAAAG | 22992 |
rs548166965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67216290 | AATAAATAGTGGAAG[A/G]GAACACGAATTTTGG | 22992 |
rs548181779 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67183095 | CCCAAATCTCTGTTT[C/T]ATTCATCCCCTTACT | 22992 |
rs548186707 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67257401 | TAGAGGTGAGGGTTG[A/G]TCCATGTGGAGGAAA | 22992 |
rs548210799 | snp | A/G | 0.000148212 | 0.00860722 | intron-variant | KDM2A | GRCh38.p7 | 11:67215475 | CCTGCATCTTCCTCC[A/G]TGTGCTGTGGGAGAC | 22992 |
rs548221629 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67222827 | AAGGAAAATACATAT[G/T]CAGTAACATAAAGTG | 22992 |
rs548238807 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67177333 | TAACTTTATATACTT[A/T]TGAACATTTTCTAAT | 22992 |
rs548239664 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67167960 | CATTTAGGGACAAAA[A/C]GTTTTATATAGATCA | 22992 |
rs548276584 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67144541 | ACAGGTGTGAGCCAC[C/T]GTGCCCGGCCCCAAC | 22992 |
rs548279714 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67186046 | CATTATAGAAGTACC[A/C]GAAGGAAAATAGAAA | 22992 |
rs548295491 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67214567 | TGGTCTTGAACTTCC[A/G]ACCTCAGGTGATCCG | 22992 |
rs548297320 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KDM2A | GRCh38.p7 | 11:67223076 | ACATGCCTGTAATCC[C/T]AGCTACTCAGGAGGC | 22992 |
rs548348369 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67257162 | CAGGGATTGTGCCGG[A/G]AGAGTGCCTCTGACT | 22992 |
rs548379346 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67254130 | GCCAGCAAGTAGCTG[C/T]TGCTGCCTGGAGCCT | 22992 |
rs548384040 | in-del | -/AAAAT | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67178245 | CCCCTGTCTCTACTA[-/AAAAT]AAAAAAATCAGCTGG | 22992 |
rs548385006 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67184487 | ACAAAAATTAGCTGG[G/T]CGTGGTGGTGGGCGC | 22992 |
rs548396503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67123926 | AGATGATCCGCCTGT[C/T]TTGGCCTCCCAAAGT | 22992 |
rs548442891 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67145550 | TATGGTAGCACCCCA[G/T]TTTTTTTTTCATTAG | 22992 |
rs548472445 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67191958 | TCTTTGGTTCCTTCT[A/G]TCATGTGCATCTTTA | 22992 |
rs548478438 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67190879 | AATAGAAAATTTGAA[A/T]AGAACTATATTGTAG | 22992 |
rs548499082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67153014 | TTGGAGACTGCGTTT[C/T]ACTCTTTCTGCCCAG | 22992 |
rs548513923 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67244139 | AGGAGTCCTGCTTGG[C/T]CTCTGCTTGGCCACA | 22992 |
rs548551588 | snp | C/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67207068 | AAATTATGGATACTT[C/T]ATTCAAATTATGAGA | 22992 |
rs548557485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206531 | TGCCTGAGCTCAGGA[A/G]TTGGAGGCCATCCTG | 22992 |
rs548566062 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67190181 | TTGGGAGGCCGAGGC[A/G]GGTGGATCACCTGAG | 22992 |
rs548581697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67228798 | TTGAATTGCAGTGGC[A/G]TGATCATAGCTCACT | 22992 |
rs548600330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67198397 | CATTTTTCCAATAGC[A/G]TATGCTCACTTCATG | 22992 |
rs548603379 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67147038 | GCTTAGTCAGATATA[A/G]ATAGCCAGAAAACCT | 22992 |
rs548608261 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67182525 | GTCAGTAAAATTGAA[C/T]AAGTCTTTTTTTTTT | 22992 |
rs548625813 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67159913 | TGTAGTATGAGATGA[G/T]GAAAAAATTCGGGAG | 22992 |
rs548662521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67159166 | TTTCATTTAGGCCTA[C/T]GATCTTTTTTGAGTT | 22992 |
rs548662881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67167420 | ATTTCTTGACCAATT[A/G]GTTTTGTGGAGGGCT | 22992 |
rs548687916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67197534 | TTTTTTGTTTCTTGG[A/G]TAGCTAATCATTGGC | 22992 |
rs548689309 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67144816 | AGTGATCCTCCTGCT[C/T]CAGCCTCCCAAAGTG | 22992 |
rs548704339 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67138815 | CAACAGCCTGTGTTT[C/T]AACTAGTTCTCCAGG | 22992 |
rs548729685 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67122953 | GTGCTGGGATTACAG[C/G]TGTGAGCCACTGCAT | 22992 |
rs548749587 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67166793 | TCAAAACTCCTGTGC[G/T]GGGCTGAGCGTGGTG | 22992 |
rs548749980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67175547 | TGTCTTTAATAAATG[A/G]GAATGGCTTGGAGAC | 22992 |
rs548809875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67229598 | AAAATGGGCCTGGCA[C/T]GGTGGCTCACACCTG | 22992 |
rs548823013 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67165062 | GCCAGGACTGTAATG[G/T]AATGGTGGTAGTGGG | 22992 |
rs548827988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67129865 | GCTGTACGCCGAGAT[C/T]GTGCCACTGCACTCC | 22992 |
rs548834180 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67183553 | GGAGTTCAGGAGTCT[A/G]TTGAAGGCTTGCAAA | 22992 |
rs548838978 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67149950 | AGGTCTTGAACTCCC[A/G]ACCTCAGGTGACCTG | 22992 |
rs548893175 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67165657 | GTGCATTTATAGACT[A/G]TCTTCTGGTTTCAAG | 22992 |
rs548949422 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67212699 | GTCTGAAGATACCTA[A/G]TAATACCAAAGAAAG | 22992 |
rs548952127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67137013 | CATTAGAGAACACTT[C/T]CCTGAGAGAGGCTTT | 22992 |
rs548979645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67143993 | GTCGCCCAGACTGGC[A/G]TGCAGTGGTGCAATC | 22992 |
rs549011016 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67245863 | TCTCCACCCTGCCTC[C/T]ATGCTTCCAGGTGTT | 22992 |
rs549030785 | snp | C/G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67220906 | AAAAAATGTAAAAAA[C/G/T]GATCCTTTTATATAG | 22992 |
rs549058672 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67134855 | AAAGCAGTCTCACAT[A/T]GTGTTTCCCACATCA | 22992 |
rs549073706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67120967 | CTTGCTAGTTGTAAT[C/T]CTGTGGGGAGAAACT | 22992 |
rs549099041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67254801 | TTTTGAAGGAAAGAC[A/G]GCTACAGGAATTGAA | 22992 |
rs549122097 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67142400 | TCATGCCTGTAATCC[C/T]AGCACTTTGGGAGGC | 22992 |
rs549122150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67134172 | AGAGAATATGAGTGG[A/G]TGAGGCTTTAGACAG | 22992 |
rs549137307 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67150750 | AGGTGAAAGATCACT[C/T]GAGTCTAGTAGTGTG | 22992 |
rs549183454 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67141977 | ATTCTCCAATTCCAT[A/C]CATGTTCCGAAAATG | 22992 |
rs549193961 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67234601 | GGGCTGAGCCCAGTG[G/T]CTCACACCTCTTGTC | 22992 |
rs549268383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67121506 | AAAGGTGTATTAATA[C/T]CGAATTTGGCTTTTG | 22992 |
rs549286740 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67202084 | AGGGGTTCAAGACTT[C/G]AGTGGAGGAAGTAAC | 22992 |
rs549364752 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67227601 | TTCAGACGGAGTCTC[A/G]CTCTGTAGCCCAGAC | 22992 |
rs549405062 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67235325 | TTTTTTTTTTTTGAG[A/G]CTGAGTTTCACTGTT | 22992 |
rs549406759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67148328 | TGGGAGGTCGAGGCC[A/G]AAGGGTCGCTTGACC | 22992 |
rs549409682 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67218016 | TTTCTTCCTGTCATT[A/G]TGGAATAGATGCTGA | 22992 |
rs549432547 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67202941 | TTGTGGCTGTGGTGA[A/G]CTGTGATTGCACCAG | 22992 |
rs549443065 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67156568 | TAGAAAAATACAGAA[A/G]ATTAGCCGGGCGTGG | 22992 |
rs549443762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67226952 | TCTAAAAGTTAAAAA[A/G]AAATGGTTTCAAAAA | 22992 |
rs549446582 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67217484 | TGGTCCCTCTTCTCT[C/T]CGAGTCCTGGATGGT | 22992 |
rs549453611 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67234130 | AGATTAATTATTCCT[A/G]TATTTGATCAGTTAT | 22992 |
rs549473350 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, synonymous-codon | KDM2A, LOC107984341 | GRCh38.p7 | 11:67117924 | GAGTCGGTCCGTGGG[C/T]AGGGCCGGCGCAGCT | 22992 |
rs549530601 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67225306 | TTGCTGAAAATGTCA[A/C/G]ATCCTAGAAAACATA | 22992 |
rs549563282 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67218372 | CTGCTAGATACTACG[C/T]TTAGAGCAAATATTT | 22992 |
rs549572174 | in-del | -/AG | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67121135 | GGAACCTGATTTTTC[-/AG]AGAGCCTTTAACACT | 22992 |
rs549599892 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | KDM2A | GRCh38.p7 | 11:67199383 | TGTCAAAAGCCAAGA[C/T]AGGCCTTTTACATCA | 22992 |
rs549631788 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67195701 | TTTAAATTCTTCAAG[A/C]AAATTGCAGTTTTCT | 22992 |
rs549675342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67194617 | GGCACCCAATACATA[C/T]TGGTGATTGCCTAGT | 22992 |
rs549682066 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67126172 | AATCGCTTGAACCCG[C/T]GAGACAGAGGTTGTG | 22992 |
rs549696497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67178763 | ATCTCATTGTATAGG[C/T]ATACCACATTTTGTT | 22992 |
rs549714656 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67143695 | TGGAGTGCAATGACG[C/T]GATCTTGGCTCACTG | 22992 |
rs549714685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67232929 | TGGCCAGGCTGGTCT[C/T]GAACTCTTGACCTCA | 22992 |
rs549763322 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67193961 | TGTCCTCCTGTCTTG[C/G]CCTCCCAAATTGCTG | 22992 |
rs549769225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67155790 | CCCAGCTAATTTTGT[A/G]TTTTTAGTATAGACG | 22992 |
rs549780879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67186788 | AAATAATTAGTAGAA[C/T]GGGGTATAGTGGTAT | 22992 |
rs549791373 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67209055 | ATTCTCCTGCCTCAG[A/C]CTCCTGAGTAGCTGA | 22992 |
rs549793548 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67119344 | CAACACCCCTCCCCG[A/G]CAGCGGCGGCGGCGG | 22992 |
rs549797248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67241371 | TGAGTTTGGGGGAAG[A/G]TGAGAGGCATCTGGA | 22992 |
rs549798535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67201494 | AATTAGCCATGGCCC[A/G]GTGCGGTGGCTCACG | 22992 |
rs549859490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67171088 | TACAGTACCTGGCAC[A/G]TGGTAGGTACTTAAA | 22992 |
rs549884560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67200921 | TTTCATGGCCTGGCA[C/T]AGTGGCTCACACCTG | 22992 |
rs549923780 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67169273 | CCATGTAGCTTTATA[C/T]AACTTTACAAAACAA | 22992 |
rs550019058 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67168419 | GTAATTCTATAATTT[A/T]TTTACATATTTGTTG | 22992 |
rs550040080 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67232266 | TATAAGAAATGTTAC[A/G]TTAAACTTAAGTTAC | 22992 |
rs550044140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67132790 | GTGTCTGGGAACATA[C/T]TAGAATGCAAATTCT | 22992 |
rs550080559 | in-del | -/T | 0.0111751 | 0.0739097 | intron-variant | KDM2A | GRCh38.p7 | 11:67170985 | TGGGCAAGTTACTTC[-/T]TTTCATTTTCCTTGC | 22992 |
rs550093509 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67140855 | TGGGTCTACTTTATG[A/G]AGAACCTTACCAGAG | 22992 |
rs550143665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67176721 | CTGAATACTATAGGC[A/G]GTTATAGCATGCCAG | 22992 |
rs550156709 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67140194 | AACATGGCGAAATCC[C/T]GTCTCTCCAAAAAAT | 22992 |
rs550199390 | in-del | -/AAAG | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67226967 | AAAATGGTTTCAAAA[-/AAAG]GCAACAAAATATATT | 22992 |
rs550205756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67146727 | GTTGCCCAGATTGGT[C/T]TTGAACTTCTGACCT | 22992 |
rs550216209 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67205728 | CAGAAGCTGTCTGCC[C/T]GTCTTGACCTCCCAG | 22992 |
rs550255993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67138752 | TGCCACTACATTCTT[A/G]GATCCTACCCCAAAC | 22992 |
rs550273273 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67256201 | CTGAGTGTATTCTGC[C/G]CGTGTGTGTGGAGGG | 22992 |
rs550290991 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67197792 | AGAACAGTGTCTGGC[A/G]TATACAGTTGACCCT | 22992 |
rs550291574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67184913 | GGATTTCAAGAGTTA[C/T]CACATTATTAAATTC | 22992 |
rs550297255 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B | KDM2A | GRCh38.p7 | 11:67258577 | GAGTGCTGGGATTAT[A/T]AGCATGAGCCACCGC | 22992 |
rs550307871 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67239358 | TACTGTACTGTGGGG[A/G]TGGAGTCCTTGTCAG | 22992 |
rs550317341 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67138213 | TAGTAAGAGTAGACT[G/T]CTGTAAGTCAAGGAA | 22992 |
rs550370098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67160877 | ACTTGGGAAGCTGAG[A/G]CAGGAGAATTGCTTG | 22992 |
rs550375193 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67234638 | CTTTAGGCGGCAGAC[A/G]CAGGCAGATCTCTTG | 22992 |
rs550380708 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67144950 | ATCTCAGCTAACTGC[C/G]GACTTTGCCTCCCGG | 22992 |
rs550392250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67216181 | CTTAGTAAATCTCAA[C/T]AGTCCTGTTTCTAGA | 22992 |
rs550411430 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67228760 | TTTTGTTTTAGAGAC[A/G]GGGCCTTGCCCTGTC | 22992 |
rs550433038 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67162295 | CAAATAAGGTCAGGT[A/G]AAGTTCATTTAATTC | 22992 |
rs550476254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67223848 | GGCTAATGGAGAGGC[A/G]TAGTGTATTATATTT | 22992 |
rs550499902 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67225822 | GTAATCCCAGCACTT[C/T]GGGAGGCTGAGGCAG | 22992 |
rs550502104 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67191182 | CAAGTAGCTGGGATT[A/G]TGCCCGGCTAATTTT | 22992 |
rs550506601 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67152875 | TTTTTAATTTTATAT[A/G]TCAGTGAGACTATAG | 22992 |
rs550516841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67247303 | CCGTGTTGGCCAGGC[C/T]GGTCTCGAACTCCTA | 22992 |
rs550519822 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67124016 | GTTTGTTGGTTTGTT[G/T]GTTTTGAGACTGAGT | 22992 |
rs550520672 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67194516 | GAAAACATTATCCCT[A/C/G]CATTATTGAGTAAAT | 22992 |
rs550528908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206348 | AGGCACAAGAATCTC[C/T]TGAACCTGGGAGGTG | 22992 |
rs550552538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67131286 | CTGAGATCTCACCGT[C/T]GCACTCCAGCCTGGG | 22992 |
rs550600815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67230092 | GAGGCAGAAGAATGG[C/T]GTGAACCCAGAAGGT | 22992 |
rs550610343 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67122874 | TAGAGACGGGGTTTC[A/T]CTGTGTTAGCCAGGA | 22992 |
rs550716041 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67158377 | AATTATGTATAAAGC[C/T]GCTCTGAATATTTAT | 22992 |
rs550730619 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67228655 | CATGCCACTGCACTC[C/T]AGCCTGGGCGACAGA | 22992 |
rs550733480 | snp | C/T | 6.65203e-05 | 0.00576678 | intron-variant | KDM2A | GRCh38.p7 | 11:67243109 | TAAGAAACTATTTTC[C/T]TTGATCTTTAGGCTG | 22992 |
rs550738369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67213667 | AAGAGGCTGAGGCAG[A/G]AGAATTGCTTGAACC | 22992 |
rs550789890 | in-del | -/A | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67142705 | GTGAGACTCCATCTC[-/A]AAAAAAAAAGTTAGA | 22992 |
rs550793051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67199997 | TCCAAAATCCTAGGG[C/T]CCTTAAGAATTATGC | 22992 |
rs550829236 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67199316 | AGGAAGAGTCCCACC[A/T]CTCTCACTTTAAATC | 22992 |
rs550846077 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67152043 | TTTCCCGCCGGGTGC[A/G]GTGGCTCACACCTGT | 22992 |
rs550855521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67235593 | CAGGCGTGACACCGC[A/G]CCCGGCTGCTTTTTT | 22992 |
rs550882789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67159073 | TGCTTTTGGTGTTGC[A/G]TCTAAAAACCCATTA | 22992 |
rs550905447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67214456 | TGATCCACCTGCCTC[A/G]GCCTCCCAAAGTGCT | 22992 |
rs550926315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67128528 | CTGGTCTCATTGTTG[C/T]GGCCTCCCTCCTAAT | 22992 |
rs550961731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67197427 | AGCAGTCAGCCCGCC[C/T]CGGCCCCACCAAAGT | 22992 |
rs550981684 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67155561 | CTCCTGCCTCAGCCT[C/G]TCAGGTTGCTGGGAT | 22992 |
rs550987727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67135896 | GAACTATGAACTGAT[A/G]TTTCTACCCACTACT | 22992 |
rs550998503 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67204366 | GTTTTCTCCTCCACT[G/T]AACTCCTGGCAACAA | 22992 |
rs551011461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67166750 | ACCAAGAAGGGAGTA[C/T]ACTGGTTCAGGTTGG | 22992 |
rs551016280 | snp | C/T | | | intron-variant, utr-variant-5-prime | KDM2A | GRCh38.p7 | 11:67186398 | GTCAACCAAGCATCC[C/T]ATATCTGGCAAAACT | 22992 |
rs551048129 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67175459 | GCACACACACACGTA[A/T]TTTTCACACTGTTGC | 22992 |
rs551094797 | in-del | -/AT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67167907 | ATGTTAAAAGTAAAC[-/AT]GTGTTTTTCCTTATT | 22992 |
rs551104025 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67254067 | GCTCACACCCTGAAG[G/T]CATGGCTGGGTGTGG | 22992 |
rs551124210 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67129010 | ATCATTTGAGCCCAG[A/G]GGCTTAAGGCTGTGA | 22992 |
rs551138702 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67182321 | AACTTTATAGGCTGA[G/T]AAGTAGATACATTAA | 22992 |
rs551142045 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67174709 | GAATATTTTTTAAGA[C/T]ATTTAAAATTCTTCA | 22992 |
rs551180936 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67165272 | GGATTACAGGCATGC[A/G]CCGCCACACCTGGCT | 22992 |
rs551188669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67136790 | TAACCATGTTCAGAT[A/G]CCATGTAGGGCGCTC | 22992 |
rs551215848 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67172205 | TTGAACTCCTGGATT[C/T]AAGTGATCCTCCTAG | 22992 |
rs551220963 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67131744 | GCTAACGTCTGTCTG[C/G]TTAACATCCTGAATT | 22992 |
rs551229482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67190054 | AAAAGATAAACAAAA[C/T]TGACAAAGCTTTATT | 22992 |
rs551248762 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67163564 | CATGTTCAAAATCAC[A/T]ATTGCTGGGCCAGAT | 22992 |
rs551282756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67254684 | TGTGCTTGTTGTCAT[A/G]TGGTGATGGGAGTGA | 22992 |
rs551284748 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67205301 | CTTACATTATTAGTT[-/A]TGTTTTACTAGTAAT | 22992 |
rs551301653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67180628 | GGATGTCATATATGT[A/G]TTGTAGTGGTCAAAA | 22992 |
rs551303704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67171441 | AGACTTTATTTTAGA[A/G]CATAATGGGGCCTTA | 22992 |
rs551305801 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67195547 | AAGAGCTCTGTTACT[A/G]TAAAGAAAATGGTTT | 22992 |
rs551340201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67179575 | GTGAGCCACCGCACC[C/T]GGCCTGGAATGCTGT | 22992 |
rs551355000 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67143421 | TCTTGGGAAGAAGCA[C/T]ATGCAGAAAAGTCCG | 22992 |
rs551400360 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67149866 | GCTGGGATTACAGGC[A/G]TGCGCCACCAGTCCC | 22992 |
rs551427544 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67155426 | CGATTATCCTGTCTC[A/C]GCCTCCTGCGTATCT | 22992 |
rs551431198 | in-del | -/G | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67225996 | TTGAACCCAGGAGGT[-/G]GGAGGTTGCAGTGAG | 22992 |
rs551448065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67157617 | AGACACAGTGGCACG[C/T]GCCTGAAATCCCAGC | 22992 |
rs551458812 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67141926 | GAACACGTGATACTT[C/G]TCTTTCTGTGCCTGG | 22992 |
rs551460025 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67126888 | GCTAGGAAATGACAA[G/T]GGTGGATAAACAATG | 22992 |
rs551493546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67149084 | AAAAGCAGATTTTTT[C/T]CCCCTGAAGCTCTTT | 22992 |
rs551503595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67220373 | TTGAGCCATGTGTTT[C/T]ATTTTTATGCTCACA | 22992 |
rs551519378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67134087 | AGACAAATGAAATAC[C/T]AAGGTAGACTTTGGG | 22992 |
rs551561801 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67147415 | GGTGTGGTGGCGGGT[G/T]CCTGTAGTCCCAGCT | 22992 |
rs551577570 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | KDM2A | GRCh38.p7 | 11:67242305 | GTGTGTGTGTGTGTG[A/T]GAGAGAGAGAGAAAG | 22992 |
rs551585530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67195659 | TATTAGTTGTTCATG[C/T]TCTATGCAGTCTGTA | 22992 |
rs551613826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67252241 | TGAGTAGCACCCTGC[A/G]TTTCAGGCAGCTGCG | 22992 |
rs551677031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67226898 | TGGGGAGGCTTTGGT[A/G]GGAGGATGATAGCCT | 22992 |
rs551712101 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67119912 | TGTTTGCTCCCTTTT[C/T]CTGGTCGCTCTGACC | 22992 |
rs551729823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67188285 | CAGGAGATCGAGACC[A/G]TCCTGGCTAACACGG | 22992 |
rs551838490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67217417 | ACTGTACTACTTAGG[A/G]CTCTGGAAGCCAGAC | 22992 |
rs551868931 | snp | C/T | | | upstream-variant-2KB, synonymous-codon | KDM2A, LOC107984341 | GRCh38.p7 | 11:67117708 | GCGTAGTGGAGCCAA[C/T]AGTGCCAACCCCGAT | 22992 |
rs551942129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67192611 | CACCATGCCTGGTCA[A/G]TTTTGTATTTTTTAG | 22992 |
rs551957576 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67240598 | CTCTCTGCCCAGGCA[C/G]CTTCTGTTCTCTTTC | 22992 |
rs551965245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67251567 | GTGGTGTCCTGACCA[A/G]TGGCATTCACTCAGG | 22992 |
rs551991094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67202763 | CCTGGGCGACAGAGC[A/G]AGACTTCGTCTCAAA | 22992 |
rs552040098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67202171 | GACTGAATTGCTGCA[A/G]TCTATAATGAAACTT | 22992 |
rs552041771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67210107 | CATGGTGGCTCATGC[C/T]TGTAATCCTAGCACT | 22992 |
rs552045565 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67239762 | TGGGCCAAGGTGCCT[A/C]GTGTAGCCCGCAGAA | 22992 |
rs552055684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67201337 | GATTCACCACTGTAG[A/G]TGCCATTAAGAACAT | 22992 |
rs552115604 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67208941 | TTTTTATTATTTATT[A/T]TTTTTTTTTTGAGGC | 22992 |
rs552168293 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67161463 | AGTACAGTGTTTTGC[A/T]CAGTTTTTAACTGAC | 22992 |
rs552179273 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67250035 | CCTGTCGGTTCAGAG[G/T]GTTTGGAAGAAAGGA | 22992 |
rs552189934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67207267 | AAATGAGACATTAGA[C/T]AAAAGAGTCAACAAC | 22992 |
rs552220155 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | KDM2A | GRCh38.p7 | 11:67258546 | CCTCAGGTAATCTGC[C/T]CGCCTCCACCTCCCA | 22992 |
rs552222047 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67191174 | CAGCCTCCCAAGTAG[C/T]TGGGATTATGCCCGG | 22992 |
rs552227447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67224651 | TTTTATATTTTTAGT[A/G]GAGATGGGGTTTCAC | 22992 |
rs552281998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67182520 | GGATGGTCAGTAAAA[C/T]TGAATAAGTCTTTTT | 22992 |
rs552339858 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67177967 | CATGGGAACACTGTC[A/T]TATATGTGCAGTTCA | 22992 |
rs552340578 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67170242 | CCAGTAGTTTGTCAA[C/T]GAAAAGCTAGAATTA | 22992 |
rs552383765 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67151871 | TACCTCAACCTCCTG[A/C]GTAGCTAGGACTATA | 22992 |
rs552404661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67176460 | CTACCACTGGCACAT[C/T]CAGTTTCCTGTTGGG | 22992 |
rs552406868 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67214963 | CTAACAATGGTATAT[A/G]TTTTGCTGAGTTTAT | 22992 |
rs552414571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67216119 | GCTAGTGTTCAGTAG[A/G]AATTAGTATTCATCT | 22992 |
rs552416585 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67168319 | TTAGGTGGAGCTTCC[C/G]CCAAACCCTCTGTGT | 22992 |
rs552421608 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67257793 | AAATGTAAGCATTAA[C/G]GGGATAAGTCTTATG | 22992 |
rs552495245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67175589 | TTGTATCCTTACATT[C/T]TCCCTATTGAAGGTG | 22992 |
rs552532394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67200797 | CAGGCATGAGCTACC[A/G]TGCCTTGCCTGAGAT | 22992 |
rs552557405 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67257680 | ATGTTTAAAGGGTTT[A/G]GTTGTGTTTTTTGTT | 22992 |
rs552569279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67146016 | TTTTTTTTTTGAGAC[A/G]GAGTCTATCTCTGTT | 22992 |
rs552593860 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67251667 | AGCAGTCTGCTTTAA[C/T]AAGCGCTCCTCCAGG | 22992 |
rs552618199 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67174003 | TACAGGCATGAGCCA[C/G]CATGCCCACTTTGGG | 22992 |
rs552657251 | in-del | -/AAAT | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67238707 | AAACAACTGTCCTGG[-/AAAT]AAATAAGAATGCTTA | 22992 |
rs552666907 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67159995 | AACTATACACAAATT[A/C]AGCTAAAATGGTAAA | 22992 |
rs552669055 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67147742 | GAGTGCAGTGGTGCA[A/G]TCTCAGCTCACTGCA | 22992 |
rs552751318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67167571 | TTCTCTTGAACATTC[C/T]GCCTTCACAGCTATC | 22992 |
rs552794445 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67190258 | CTACTAAAAATACAT[A/G]AATTAGCTGGATGTG | 22992 |
rs552831999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67123973 | TGAGCCACTGGACCT[A/G]GACTTTTGGGTTTTG | 22992 |
rs552838430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67150128 | TTCTTTACAACCCTA[A/G]ACAAGTTTAATTAAA | 22992 |
rs552846225 | in-del | -/T | 0.0681886 | 0.171594 | intron-variant | KDM2A | GRCh38.p7 | 11:67145998 | TTTTGTTTTTTTTTG[-/T]TTTTTTTTTTTTGAG | 22992 |
rs552865293 | in-del | -/ATCC | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67196163 | TTCTAACAAGACATA[-/ATCC]ATCCACTACAGTGAA | 22992 |
rs552875984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67149306 | CATTTCTAAAGTGCA[A/G]GTGGTACTGATACCT | 22992 |
rs552877774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67157669 | AGGATCGCTGGAACT[A/G]GGGAGGTGGGGTTTG | 22992 |
rs552893402 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67130635 | TCTTTGTATCTTTCT[A/G]TTTTGGGGGGGTAAC | 22992 |
rs552897619 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67221401 | AGTATTAAAAATTTT[A/T]AAATAACAATTAATG | 22992 |
rs552913837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67123115 | GCTGGGACTACAGGC[A/G]TGTGCCACCATGCCA | 22992 |
rs552927103 | snp | G/T | 0.0023933 | 0.0345097 | downstream-variant-500B | KDM2A | GRCh38.p7 | 11:67258470 | TGTGTGTGTGTGTGT[G/T]TGTGTATTTTTGTAG | 22992 |
rs552943909 | snp | A/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67184517 | CCTGTAATCCCAGCT[A/G]CTCAGGAGGCTGAGG | 22992 |
rs552978478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67143146 | CTTGCGTCAGCATCC[C/T]GAGTTGCTGGGATGA | 22992 |
rs553002503 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67156913 | AATATGAAATAGGAG[C/G]TTCAGTGCCCACAAA | 22992 |
rs553005169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67196952 | ATTTCTGAGCTATGC[A/G]AATATGTAAGATCTT | 22992 |
rs553016868 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255321 | TCGAGGCGCCTGCTC[A/G]CTTACTCGCCTGCCA | 22992 |
rs553026588 | in-del | -/AG | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67121940 | ATAGATCTTGTTGAA[-/AG]AAATTTTAGACATGA | 22992 |
rs553031851 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67220261 | AAGTGATCTGCCCGC[C/T]TTGGCCTCCTAAAGT | 22992 |
rs553035726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67253704 | AAGGTAGTCTCAGAT[A/G]TGACGCTGTGGAAGA | 22992 |
rs553039638 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67121023 | CTGAAACCAACATCT[C/G]GTTTCGTCTAGGCCT | 22992 |
rs553040199 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67121910 | AAGTTCTGTGTTTTG[C/G]GAGGAATGTACGAGA | 22992 |
rs553066816 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67123654 | ACTTTAAAGGAAGAG[C/G]CTTTCCAGCAAGCAA | 22992 |
rs553080153 | in-del | -/AAAAAAAAA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67195386 | AAAAAAAAAAAAAAA[-/AAAAAAAAA]GTTGAATAACATTAA | 22992 |
rs553102826 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67127784 | GCAATCTGGGCTCAC[C/T]GCAACCTCCCTCTCC | 22992 |
rs553118416 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67187855 | CTGGGGATTATAGGC[A/G]TGAGCCATGGCACCG | 22992 |
rs553130154 | snp | A/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67121024 | TGAAACCAACATCTC[A/G]TTTCGTCTAGGCCTC | 22992 |
rs553130432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67235713 | TGCAGCCTCCACCTC[C/T]TGGGTTCAAGTGATT | 22992 |
rs553152792 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67156788 | CAGCTACTGAGGAGG[C/T]TGAGTCAGGAGAATC | 22992 |
rs553157635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67197598 | TTTCAGCCTGTGGTG[A/G]AATGTTACTTCTTCA | 22992 |
rs553160156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67234644 | GCGGCAGACGCAGGC[A/G]GATCTCTTGAGACCA | 22992 |
rs553218117 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KDM2A | GRCh38.p7 | 11:67154025 | TACCACAGATTTACG[A/G]TTATACTGAAGAAAA | 22992 |
rs553241826 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67233837 | AAGAGGAGGCTTAGC[A/G]TTATGAAAAGTGTCC | 22992 |
rs553249872 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67126573 | ATTAGCCGGATGTGG[C/T]GGCAGGCGCCTGTAG | 22992 |
rs553253765 | snp | A/G | | | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67238575 | TCAGCCGAGAGCACA[A/G]AAGTCTGTCCTTCCC | 22992 |
rs553259140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67244271 | GTCCTTGTCCTTGAA[A/G]AGGTCACCAGCAGGG | 22992 |
rs553280509 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67242808 | TGATAATATTGCAGC[A/C]GCCTAAGTTTGAGTT | 22992 |
rs553301497 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67226461 | GGCGCAGTGGCTCAC[A/G]CCTGTAATCCCAGAA | 22992 |
rs553307061 | in-del | -/GTG | 0.00194584 | 0.0311309 | cds-indel, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255487 | CATGGCCAGGTTCTT[-/GTG]GTGTCCAGTGCGCGT | 22992 |
rs553308683 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67216875 | CGGTGAGCTGAGATC[A/G]CGCCATTGCACTCTA | 22992 |
rs553313415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67133787 | GCTTACTATAACTTC[C/T]GCCTCCCAGGTTCAA | 22992 |
rs553318266 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67204617 | CTGCCTCAGTCTCCC[A/G]AGTACCTGGGACTAC | 22992 |
rs553364920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67212778 | TCTGTGAATGAATGC[A/G]TGGTAAAAAAAAAAA | 22992 |
rs553384141 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67164487 | CCTTTTTTTGTTGTT[C/G]TTGTTTTTTTGTAGC | 22992 |
rs553423928 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67172980 | AGACATAATGTGATG[A/C]ACTGGTTTTTATTTT | 22992 |
rs553466811 | in-del | -/TG | 0.0275971 | 0.114179 | downstream-variant-500B | KDM2A | GRCh38.p7 | 11:67258462 | TAATTTGTGTGTGTG[-/TG]TGTGTGTGTGTGTAT | 22992 |
rs553491463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67210939 | TTGAGCCCAAGAGTT[C/T]GAGACCACTCGGGAG | 22992 |
rs553504958 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67227115 | ATAATGAAAATGCTC[C/T]TTTGGGAAGAATGGA | 22992 |
rs553512653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67141229 | GCGAAACAATTTTTC[C/T]ATATTGTTTTGGGGG | 22992 |
rs553514713 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67195070 | GGACCTAGACAGAGG[A/C]AATAACCTAAAGACA | 22992 |
rs553559598 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67213204 | TTTATGCATTTGTCT[C/G]CATTCACATTATAAG | 22992 |
rs553574164 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67147672 | CTGAGTAGTTCCCTT[G/T]CATTAGAGATTCTTT | 22992 |
rs553585596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67180859 | TAGAGACGGGGTTTC[A/G]CCATGTTGGCCAGGC | 22992 |
rs553594487 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67249021 | ACAGGAGGAGATGGC[C/T]TTCCAAGTGCCAGTC | 22992 |
rs553599237 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67208507 | CAGGCGCAGTGGCTC[A/T]TGCTTGGAATCCCAG | 22992 |
rs553600381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67202380 | TGAAAGACGTTCTAC[C/T]ATGGGTAAAATGATA | 22992 |
rs553655910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67233431 | GGCCGAGGCAGGTAG[A/G]TCACGAGGTCAGGAG | 22992 |
rs553690536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67142061 | CATTCATTTTTGAGA[C/T]GGAGTCTTGCTGTGT | 22992 |
rs553697963 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67221392 | AGAATTAAAAGTATT[-/A]AAAATTTTAAAATAA | 22992 |
rs553703256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67179387 | CAAGCGATTCTCCTG[C/T]GTCAGCCTCCTGAGT | 22992 |
rs553703458 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67187945 | CACACCTAAAATCCC[A/G]GCACTTTGGGAGGCT | 22992 |
rs553757968 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67202998 | AGACCCTGTCCGTCC[A/G]CCGCCAAAAAAAAAA | 22992 |
rs553784110 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67244588 | GCCAAAGGGCTAGGA[C/T]AAGGGCTGGTAAATT | 22992 |
rs553816896 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67186392 | AAAACTGTCAACCAA[C/G]CATCCTATATCTGGC | 22992 |
rs553820107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67169819 | CTAGAGTACAGTGGC[A/G]AGATCTCGGCTCACT | 22992 |
rs553841565 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67208999 | AGAGTGCGGTGGCAC[A/G]ATCTCGGTTCACTGC | 22992 |
rs553852977 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67224998 | AGGTATGCACCACCA[C/T]GCTAATTTTTGTATT | 22992 |
rs553858148 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67147245 | ATGGTCAGGTTAAAA[C/G]ATATGACTTCCACTG | 22992 |
rs553877263 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67175278 | CAGTGTTAAAATTCA[C/T]ACAGGCCAGGTGTGG | 22992 |
rs553884585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67201898 | AATTCGAGGTTGCAA[C/T]GAGCTCTGATCTTGC | 22992 |
rs553937284 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67193231 | CTGACCTCAGGTGAT[A/C]CACCCGCCTCAGCCT | 22992 |
rs553959111 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, missense | KDM2A, LOC107984341 | GRCh38.p7 | 11:67118087 | CGCGCACCCCTCCGT[G/T]GGGGGCGCCCCGACT | 22992 |
rs554006085 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67154362 | GGTATTTAGTATATT[C/T]AAAATGTTTTGCAAT | 22992 |
rs554021408 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67133133 | AGAGGGAGTTTCACT[C/G]TTGTTGGCCAGGCTG | 22992 |
rs554022191 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67155284 | GGCATAAGCCACTGC[A/G]CCCCAGCCTAGCAGT | 22992 |
rs554043302 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67201111 | AGGCAGGAGAATGGC[A/G]TGAACCCGGGAGGCG | 22992 |
rs554043325 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67132697 | TAGCTTGCCTTTTGA[A/G]GTGACAGGAACCCTG | 22992 |
rs554095744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67146251 | GCCTGCCTCAGCCTC[C/T]CAAAGTGCTGGGATT | 22992 |
rs554138614 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67228938 | CTCTGTTGCCCAGGC[C/T]GGTCTTAAACTCCTG | 22992 |
rs554157502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67160261 | TAGCCTCGAGGGATC[A/G]TTATTGATGTCTCTG | 22992 |
rs554189801 | snp | A/C | 0.000798403 | 0.0199641 | missense, nc-transcript-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67207544 | TGTCATGGACGTGAA[A/C]ACACAGAAAGGCATT | 22992 |
rs554194396 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67159704 | CAATATTTGTCAGGC[A/G]TTTGATAGGTACTGG | 22992 |
rs554195424 | in-del | -/TTTA | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67232484 | TTATCAAGTTTTATG[-/TTTA]TTTATTTTTTAATTA | 22992 |
rs554199022 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67136234 | GATTCTTTGACTCCC[A/G]TTTTAAAGTTTTGGA | 22992 |
rs554207002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67177547 | ATCAGTATCACAGAG[C/T]GGCATCATTATCACT | 22992 |
rs554285645 | in-del | -/AAAAC | | | intron-variant | KDM2A | GRCh38.p7 | 11:67148803 | CAAAATTCCGTCTCA[-/AAAAC]AAAACAAGACAGACA | 22992 |
rs554340628 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67240028 | CACTCTCGCTCGGCT[C/G]CCCCTCCTGCCATCT | 22992 |
rs554355955 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67130441 | TGAGCCACCATGCCC[G/T]GCCTTAAGCTCTCCT | 22992 |
rs554393501 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67202740 | GAGATCGCGCCACTA[C/G/T]GCTCCAGCCTGGGCG | 22992 |
rs554393752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67166687 | GTATACAGATCAGGT[A/G]TCTGTACTAAGTTTG | 22992 |
rs554406909 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67127711 | ATTAATTAATTTATT[A/C/T]ATTTATTTATTTTGA | 22992 |
rs554419106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67129551 | CATCCTGGCTAACAC[A/G]GTGAAACCCCGTCTC | 22992 |
rs554428068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67249850 | AATTAAAAATGGTCA[A/G]GCCAGGTGCAGTGGC | 22992 |
rs554442940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67230163 | CCTGGGTGACAGAGC[A/G]AGACTCCGTCTCAAA | 22992 |
rs554454616 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67234922 | GAAGCTGAGGCGGGC[A/G]GATCATGAGGTCAGG | 22992 |
rs554464511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67200496 | TGCTGGGATTATAGG[C/T]GTGAGCGACCGTGCC | 22992 |
rs554474405 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67247394 | CGCACCCAGCCTGAT[A/T]CTTAGGATATTTTAA | 22992 |
rs554480611 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67137634 | TTATTGAAATAGGGT[A/G]CACTGAAGGAAGAGC | 22992 |
rs554492414 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67257029 | TATCGTTAATGACCT[A/G]TAATTGGAAGCTTCC | 22992 |
rs554495092 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67257131 | TAAAAGGGGAGGTGG[A/C]GAGACCCCTTCAGAG | 22992 |
rs554564376 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67246480 | AGTGTACCTCTGGAT[A/G]TTAGTTCCTAAGGGA | 22992 |
rs554564456 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255670 | GTTCTGCCCAGCACT[C/T]GTGCTTGTTCACATA | 22992 |
rs554606732 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67145084 | ACCATGTTGGCCAGG[C/T]GGGTCTTGAACTCCT | 22992 |
rs554653526 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67215738 | GCTTTTTCTCCTTCT[A/C/G]GAACTTAAGATTAAG | 22992 |
rs554690683 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67223261 | TGATATGCGGCATAA[A/G]TAAAAAGCAATGGGG | 22992 |
rs554694264 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67183854 | TGGGTCATGCCTGTA[A/T]TCTTAGCACTCTGGG | 22992 |
rs554713164 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67124317 | CTTCACTTTATTTTT[A/G]TATATATTTTTTGAA | 22992 |
rs554726353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67176076 | ATCAAAATTAAACCT[C/T]CTTTTGGCTTTTGAA | 22992 |
rs554747806 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67216552 | CTTGTTACTCTTTTT[C/T]CTCTAACTTGCAGTG | 22992 |
rs554758554 | in-del | -/T | 0.172674 | 0.237741 | intron-variant | KDM2A | GRCh38.p7 | 11:67167586 | GCCTTCACAGCTATC[-/T]TTTTTTTTTTTCCTT | 22992 |
rs554760775 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67229818 | GAGGTTGCAGTGAGC[C/T]GAGATCACGCCACTG | 22992 |
rs554778528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67222714 | TACCCATTCTAAGAT[C/T]CAGTCTGAAAATTGG | 22992 |
rs554784612 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67213690 | CTTGAACCTGGGAGG[C/T]GGAGGTTGCAGTGAG | 22992 |
rs554789044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67221346 | GAAGAGTGTAGAACT[A/G]TTAATGCTACTGCTC | 22992 |
rs554814410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67150364 | TACCACCACCTTGTT[A/G]GGCCAAAGGAGAGGT | 22992 |
rs554842797 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67237031 | TGAGAGTGGCAGAGT[C/G]TATCCTGAGGGAAAG | 22992 |
rs554868305 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67249322 | AATACATTGGAAAAG[A/G]TAGCACCCAAAAGGT | 22992 |
rs554872155 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67183851 | CAGTGGGTCATGCCT[A/G]TAATCTTAGCACTCT | 22992 |
rs554904305 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67245849 | CAAAACCTCCGTTCT[C/G]TCCACCCTGCCTCCA | 22992 |
rs554906331 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67183203 | GGTGCTCAGTAAATC[A/C/T]GTTGAATAATGAAAA | 22992 |
rs554907447 | in-del | -/T | 0.16846 | 0.236329 | intron-variant | KDM2A | GRCh38.p7 | 11:67147684 | TTTCATTAGAGATTC[-/T]TTTTTTTTTTTGAGA | 22992 |
rs554911921 | in-del | -/TTTTTTT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67214207 | ACCATGCGCAGCTAA[-/TTTTTTT]TTTTTTTTTTTTTTT | 22992 |
rs554924001 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67238694 | CAGAAACTCACTCAA[A/G]CAACTGTCCTGGAAA | 22992 |
rs554954554 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67227281 | CCCTAGACTAGACAC[A/G]GTCTGAGAGTGAGTC | 22992 |
rs555007316 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67235664 | TCTTGCTCTGTCACC[C/T]AGGCTGGGGTGCAGT | 22992 |
rs555008803 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67151498 | GGGTTACAGGTGTCT[G/T]CCATAATGCCTGGCT | 22992 |
rs555041077 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67172936 | ACCACATCTCAAAAA[A/G]GAAAAGAAAAAAATT | 22992 |
rs555044839 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67200381 | CCACCACGTCCGGCT[A/G]ATTTTTTTCGTATTT | 22992 |
rs555048336 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67188488 | CTCTGTCTCAAAAAA[A/C]AAAAAAAAGAAAGAA | 22992 |
rs555062572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67205505 | AAATTTTTTTTTTCT[A/G]CAGCCTCGACCTCCT | 22992 |
rs555135228 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67196791 | GAGATGGATGGTGGT[A/G]ATGGTTGCACAACAT | 22992 |
rs555135651 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KDM2A | GRCh38.p7 | 11:67181187 | TAAGCATATATTTTA[C/T]TGACTAACAGCATAA | 22992 |
rs555170272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67234889 | TGGTGGCTCATGCCT[A/G]TAGTCCCAGCACTTT | 22992 |
rs555173805 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67196101 | ACGAACATAATTGTC[A/G]GTCATAAATTGAGGA | 22992 |
rs555187749 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67157769 | AAAAAAAAAAACTTG[C/G]ATTAGTGTTGTACAT | 22992 |
rs555195372 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67169818 | GCTAGAGTACAGTGG[C/T]GAGATCTCGGCTCAC | 22992 |
rs555216088 | in-del | -/ACT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67137499 | ATTGATTCTATGAGA[-/ACT]ATATATGAAATAGAA | 22992 |
rs555231228 | snp | A/G | | | intron-variant, utr-variant-5-prime | KDM2A | GRCh38.p7 | 11:67132019 | AAGATAAAAGGCAGC[A/G]AATAGTGACCAAACG | 22992 |
rs555313679 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67228221 | TCTGAGGGTGAGGCC[C/T]GAAATACTCAGTAGG | 22992 |
rs555329473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67163312 | ATCGGTGGCAGGATA[C/T]AGTTGTTGAATTTCA | 22992 |
rs555338591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67181843 | CTGGTGTTTGTTTCA[C/T]AGAATGCCGGATCCA | 22992 |
rs555357328 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67128552 | TCCTAATAATGTAGG[A/C]AAAACTTGACCATTT | 22992 |
rs555376899 | in-del | -/ATTTATTT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67187584 | TTTATTTATTTATTT[-/ATTTATTT]TGAGATGACGTCTTG | 22992 |
rs555433407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67210850 | GTCAAGTTTTACATT[C/T]ATAGCTAGAGGCCTG | 22992 |
rs555479700 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67135128 | GGCTGGAGTGCAATG[C/G]CGCGATCTCGTCTCA | 22992 |
rs555502220 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67244786 | GTCAGGAGATTGAGA[C/G]CATCCTGGCTAACAT | 22992 |
rs555532754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67244114 | GAATCACCTCCTCGT[C/T]CCTAGTGGGAGGAGT | 22992 |
rs555619081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67133080 | ATCAAGTCTCTTACC[A/G]ATTGTGCTTTTATTC | 22992 |
rs555619139 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67141068 | CTTTCTCAGTTTATC[C/T]CCCTCTCTTTGGAGT | 22992 |
rs555619331 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67193042 | TTTCTCAGTCTGGAG[C/T]GCAGTGCCGCGATCT | 22992 |
rs555620520 | snp | G/T | 3.31268e-05 | 0.00406968 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67253487 | AGCAGGCTGCTCCTG[G/T]TCTGCAGTCTCTGCC | 22992 |
rs555637620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67126524 | ACCAGCCTGACCAAC[A/G]AGGTGGAACCCTGTC | 22992 |
rs555657278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67252924 | AAGAAAAGTTGCATT[A/G]TTGGCAGTGCTTCTT | 22992 |
rs555658345 | in-del | -/A | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67238606 | CTGGTAAACTACTAT[-/A]AAAATAACATATGTA | 22992 |
rs555680337 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67140431 | CCTGAGCAACATAGC[A/G]AGACTGTCTCAAGAA | 22992 |
rs555690374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67233392 | AGTGCGATGTCTCAT[A/G]CCTGTAATCCCAGCA | 22992 |
rs555717034 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67187180 | AAATGAGAAAGGAAT[A/T]TACACATTTCACCAA | 22992 |
rs555809719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67203258 | TGTACACTTAATAGC[C/T]TACAGTATAATGTAA | 22992 |
rs555822592 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67127084 | TGTTCTGAGGTAACA[A/G]TGATTTATTTCTGTA | 22992 |
rs555852264 | snp | A/G | | | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67239437 | TTATTGAATATCTCA[A/G]TATTGGCTGACATGG | 22992 |
rs555869940 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67170372 | TTGCTAATCCTTTAT[A/C]CTACCAAGCATGGGG | 22992 |
rs555881725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67226444 | AATCAGATTTCCAGC[C/T]AGGCGCAGTGGCTCA | 22992 |
rs555908524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67147043 | GTCAGATATAAATAG[C/T]CAGAAAACCTAACAG | 22992 |
rs555943572 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67155202 | TGTATGTTTTGTAGA[A/G/T]ATGGGGTTTTGCTAT | 22992 |
rs555944556 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67224886 | CGCTGCTGTTGTCCA[A/G]GCTGGAGTGCAGTGG | 22992 |
rs555959613 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67244708 | AGCCATTGATTGGCC[A/G]GGTGTGGTGGCTCAC | 22992 |
rs555966030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67208460 | GACCTTTGGATGTAA[C/T]GGAGAGGAATATTAA | 22992 |
rs555985556 | in-del | -/TGTGTA/TGTGTGTA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67201234 | GTGTGTGTGTGTGTG[-/TGTGTA/TGTGTGTA]TATATATATATATTT | 22992 |
rs556011998 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67174275 | AAAAAAGAAAGAAAC[C/T]GTTTCCTAAAAACAG | 22992 |
rs556022285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67224161 | TCCTATCCAGTTCTC[C/T]GTGATTCAGGAACAC | 22992 |
rs556052045 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67149459 | CAGTTTTACGCCTTT[C/T]AAATCTGATTTTTTA | 22992 |
rs556058919 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67147528 | GCCTGGGCGACAGAG[C/T]GAGACTCCGTCTTAA | 22992 |
rs556109554 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67231136 | TAATTTTTTTAATGT[A/G]GAGATGGGGTCTCAC | 22992 |
rs556114596 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67194821 | GTTGCAGCAGGGTTT[C/T]AGGAGGATCCTATTT | 22992 |
rs556146426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67230494 | AGCTGAGTGTTGGGG[C/T]ACATGCCTCTGGTCC | 22992 |
rs556172648 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KDM2A | GRCh38.p7 | 11:67193057 | TGCAGTGCCGCGATC[C/T]CGGCTTACTGCAACC | 22992 |
rs556186069 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67189335 | ATTAGAAAATACTTA[C/T]AGATGAATGAACACA | 22992 |
rs556190846 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67177458 | TCTACTAAAGTTTTT[G/T]TTTTAACTTTTTAAA | 22992 |
rs556238675 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67201814 | AAAAAAATTAGCCAT[G/T]CTTGGTGGTGTACAC | 22992 |
rs556278624 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185635 | CGAGCGAAACTCTGT[C/T]GCAAAAAAAAAAAAA | 22992 |
rs556282804 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67122781 | CCTGGGTTCACACCA[G/T]TCTCCTGCCTCAGCC | 22992 |
rs556293055 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67239910 | TGTGGCTGAGCTCTC[C/T]TCCCTGGCAGGGCCT | 22992 |
rs556320529 | in-del | -/AAAA | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67184626 | AGCGAGACTCATCTC[-/AAAA]AAAGGTGAGTGGAGG | 22992 |
rs556337963 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67130397 | TGATCCGCCCACTTC[A/G]GCCTCCCAAAGTGTT | 22992 |
rs556368019 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67216417 | CTTTTTGAGGATGTA[A/G]ACAGGTTTTGAAGGA | 22992 |
rs556383890 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67199689 | GTTTAAGAAACCATC[C/T]TTGTAACAATGAAGT | 22992 |
rs556427859 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67163329 | GTTGTTGAATTTCAT[-/A]AAATTTCATCCCTAG | 22992 |
rs556491110 | in-del | -/T/TT | 0.496707 | 0.230345 | intron-variant | KDM2A | GRCh38.p7 | 11:67130129 | ACCCCACCTGGCTAA[-/T/TT]TTTTTTTTTTTTTCT | 22992 |
rs556496851 | in-del | -/AAAGA | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67222758 | TCCCTTTTTATGGTT[-/AAAGA]AAAGATGACTCTTAC | 22992 |
rs556515422 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67177044 | GGGCGGATCACCTGA[C/G]GTCAGGGGTTCAAGA | 22992 |
rs556521080 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206778 | CTCTTTGACTCCAAA[G/T]CTATTGTTTTCTCTC | 22992 |
rs556521642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67167046 | TCATACCATTGCACT[C/T]CAGCCTAGGCGACAG | 22992 |
rs556537000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67160130 | GCTTCCTGTTGGTCT[A/G]TTAGGACTAATTGGG | 22992 |
rs556537900 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67132660 | CAGTTTCAGGTCGGG[A/G]TGGTCTAGAAAGAAA | 22992 |
rs556610054 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67175856 | TACTTATTCTAGTAG[A/C/T]ATTGCTCTTGCTTTA | 22992 |
rs556610129 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67166429 | GACCTCAAGTGATCC[G/T]CCCGCCTTGGCCTCC | 22992 |
rs556615288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67139627 | CAAGTGATCCTTCTG[C/T]CTCAGCCTCTCAAAG | 22992 |
rs556645337 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67175042 | TTGTATTATTTGGTA[A/T]TGTTGATGGGCTAGA | 22992 |
rs556652343 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67248570 | ATTGTGTTTTGTATT[A/G]CTAAATGTTGTTCCA | 22992 |
rs556675310 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67139159 | ATTACTACGCCCTTC[C/G]TGGTGACACCAGTTA | 22992 |
rs556705818 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67225742 | CCACTGGACTCTAGC[A/C]TGGGCAATAAGCACA | 22992 |
rs556736284 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67199914 | TGACTCTCTTGTTAG[G/T]GGCTAATGCAGCTGG | 22992 |
rs556736747 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67145719 | CATTACTTGAAAATG[A/C]TACCATACTCGGCTA | 22992 |
rs556779275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67196601 | AATCCTAAGGACTTA[C/T]GCTAAGTGAAATAAC | 22992 |
rs556791944 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67183775 | TGGGATCCATGCTGT[G/T]GTCACTGAGTGCTGC | 22992 |
rs556797074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206180 | TCACATGTGTAATCC[C/T]AGCATTTTGGAAGGC | 22992 |
rs556820410 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67257039 | GACCTATAATTGGAA[C/G]CTTCCTGCCTTTTTC | 22992 |
rs556840835 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67205454 | CATCCAGCCAGGGCA[C/G]GTGTTTGTTCGTCTT | 22992 |
rs556855245 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255811 | GGACACACCCATTTC[A/G]TTGCTACCCAAGTGG | 22992 |
rs556867492 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67230691 | CACATCTGTTAAAGC[A/G]TGGAAAGAAAGTATA | 22992 |
rs556876328 | snp | C/G/T | 0.000145059 | 0.00851532 | missense, synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255028 | CTACTGCCTGTCTGA[C/G/T]GAGAAGCTGATACAG | 22992 |
rs556880599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67143707 | ACGCGATCTTGGCTC[A/G]CTGCAACCTCTGCCT | 22992 |
rs556885095 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67214858 | TATTCCTAAGCTGGT[A/C]GTTTCTATAGCACAT | 22992 |
rs556906153 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67227799 | TGGTCGCGAACTCCT[C/G]ACCTCAAGTGATCCA | 22992 |
rs556915544 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67224296 | CTTATCCTTTTGAAA[G/T]ATGGCCTCTCTAAAA | 22992 |
rs556932994 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67157042 | TAATTGGCTGGGCAC[A/G]GTGGCTCACGCCTGT | 22992 |
rs556955867 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67136423 | TTGAGGGTGTTTCCC[A/C]AGTCATCTGTTCTCA | 22992 |
rs556994653 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67189790 | GGTTGCAGTGAGCCA[A/G]GATCGCACATTGCAC | 22992 |
rs557001410 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67220898 | CAACCATTAAAAAAT[A/C/G]TAAAAAACGATCCTT | 22992 |
rs557015051 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67188009 | ACCAGCCTGGGCAAC[A/G]TACCAAGACCTCATG | 22992 |
rs557016360 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | KDM2A | GRCh38.p7 | 11:67122641 | GCCTATTTTTTATTT[A/T]TTTTTATTTATTTAT | 22992 |
rs557030536 | snp | A/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67121219 | CTCATTTCTGCTTAT[A/G]TCATTATTCTTTAGT | 22992 |
rs557078108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67129456 | TAGCCGGGCATAGGC[C/T]GGGCGCGGTGGCTCA | 22992 |
rs557085518 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67221544 | TTGGTGTAGGAGTTA[C/T]GTATCACTATACACA | 22992 |
rs557101551 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67121644 | CAATGTGACAAAGAT[A/T]CCTGATTTTACAGTA | 22992 |
rs557122337 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67126115 | GCCGAACGTGGTGAC[A/G]CATGCCTGTAATCCC | 22992 |
rs557122338 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67228896 | TATGCCCAGCTAATT[C/G]TTACTTTCTGTAGAG | 22992 |
rs557135566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67236545 | TAACAATATATCTGG[C/T]GGCCCAGCTCACTTA | 22992 |
rs557137708 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67159469 | TAGATTCATCTTAAA[C/G]ATTTTGGCAAGAATG | 22992 |
rs557156109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67190353 | AAGCAGAGGTTGCAG[C/T]GAGCCAAGATTGCAC | 22992 |
rs557211986 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67123801 | CTTGTCTCAGCTTCC[C/T]GAGTAGCTGAGATTA | 22992 |
rs557218808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67157466 | TTAACATCTTGTGGC[C/T]GGGTGCAGTGGCTCA | 22992 |
rs557260977 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67234722 | TCCAGGTGTGGTGGT[A/G]TGTGTTTGTGATCCC | 22992 |
rs557276041 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67219696 | GTAGCTGGGACCGTG[G/T]GTGCACACCACATCT | 22992 |
rs557303294 | snp | A/C/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185483 | AAAATACAAAACTTA[A/C/G]CTGGGCATGGTGGTG | 22992 |
rs557348653 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67234121 | AGATCAAATAGATTA[A/G]TTATTCCTATATTTG | 22992 |
rs557351420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67205489 | GGAAGACAATAGATA[C/T]AAATTTTTTTTTTCT | 22992 |
rs557368935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67196670 | CATGAAGTATATAGA[A/G]TAACCAAAATCATGG | 22992 |
rs557382579 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67157716 | CGCCACTGCACTCCA[G/T]CCTGGGCGACAAAAG | 22992 |
rs557427438 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67127286 | TTTTTCTGTAAAGGC[A/G]GGCTATCCCTGTTCG | 22992 |
rs557490263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67203041 | GGTTTACACTTCAGC[A/G]AAAGAAAAAGAAGTT | 22992 |
rs557497212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67220616 | CAGCTAATACCCTTC[C/T]AGATGCATAGAAAAA | 22992 |
rs557505070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67187976 | GAGGCAGGACTGCTT[A/G]AAGCCAGGAATTCAG | 22992 |
rs557519536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67242864 | TTTTCCAGTGAGTCT[C/T]TATATGAAGGGCAAA | 22992 |
rs557536472 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67165305 | TTTTGTATTTTTAGT[A/G]GAGACGAGGTTTCTC | 22992 |
rs557577715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67202425 | ATGCTACAGAGAAGT[C/T]TCTTTGTGAAAGGAA | 22992 |
rs557587938 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67162649 | GACCTCAAGTGATCC[A/G]CCCGCCTCGGCCTCC | 22992 |
rs557590295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67196014 | TCAGAACCACAAGAA[C/T]TGCTAAATTTCTCTC | 22992 |
rs557608443 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67209664 | GGCCAGGCTTGTCTC[A/G]AACCCCTGACCTCAG | 22992 |
rs557608552 | snp | A/G | 7.40658e-05 | 0.00608502 | intron-variant | KDM2A | GRCh38.p7 | 11:67252601 | AGAACGAGCCTCCAG[A/G]TACTCTGCTTTTCCC | 22992 |
rs557627754 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67127933 | CTGGTTTCAAACTCC[C/T]GACCTCAGGCAGGCG | 22992 |
rs557644195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67181125 | GAAAACCCCTCAAGC[A/G]TTGCTTCTCAATGTG | 22992 |
rs557726025 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67126396 | TCTGGGCAACATAGA[C/T]CCCCGTTTCTCACAC | 22992 |
rs557747856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67243818 | GAAACTGTCTCAAAG[A/G]AAAAAAAAGAAGAAG | 22992 |
rs557796096 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67179139 | TTTGGTTTGCATTTT[G/T]CTAATGACTAATGAG | 22992 |
rs557802315 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67169934 | GGCTAATTTTTGTAT[G/T]TTTAGTAGAGATGGG | 22992 |
rs557804343 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67188310 | ACACGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 22992 |
rs557809574 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67162631 | GACTGGTCTCGAACT[C/G]CTGACCTCAAGTGAT | 22992 |
rs557868822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67225639 | GCCAGGTGTGGTGGC[A/G]CATGCCTGTAATCCC | 22992 |
rs557950739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67156688 | GGCGCCTCTGCACTC[C/T]AGCCTGGGCAACAGA | 22992 |
rs557952670 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67129216 | AACGTATGTGTAGCA[A/C]ACATGTCAGACTACC | 22992 |
rs558002157 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67147726 | AGTGTCGCCTGAGCT[G/T]GAGTGCAGTGGTGCA | 22992 |
rs558009915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67218298 | TCAAAGTAAGTGCTT[A/G]TAAAGATCACAGATT | 22992 |
rs558053292 | in-del | -/CT | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255859 | ATCTCCTTGTTCCCC[-/CT]CTCTCTTTTGCCTCC | 22992 |
rs558060253 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67155090 | TGCCATCTTGGCTCA[C/T]TGCAACCTCTGCCTC | 22992 |
rs558067164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | KDM2A | GRCh38.p7 | 11:67186403 | CCAAGCATCCTATAT[C/T]TGGCAAAACTGTCCT | 22992 |
rs558120059 | snp | C/G | 6.67067e-05 | 0.00577485 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67250330 | TGCTGCGGCTGCAGG[C/G]CACAGAGCGCACCAT | 22992 |
rs558146293 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67154486 | TGCCTAGGCTGGAGC[G/T]CAATGGCGTGATTTC | 22992 |
rs558158260 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, synonymous-codon | KDM2A, LOC107984341 | GRCh38.p7 | 11:67118488 | ATGGCGGGCAAGCCG[G/T]CCTCGGCCCACCGGC | 22992 |
rs558208078 | in-del | -/TT | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67232682 | AATCCAGACTTGAGC[-/TT]TTTTTTTTTTTTTTT | 22992 |
rs558235020 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67187015 | CATCAGTAACCAAAA[A/G]GGGTAGAGACAGAGC | 22992 |
rs558289762 | snp | C/T | | | intron-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67120612 | GTCCTTGATTTGCAC[C/T]TCTGAAATTTGTTTC | 22992 |
rs558305544 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67125172 | AGCCTGGAGGGAACT[C/T]TCTTTTTTTTTTTTC | 22992 |
rs558324802 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67161090 | CTAGTGGCCAGGCAC[A/T]GTAATTCACACCTGT | 22992 |
rs558328701 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67153565 | GTAAAGAACATCTGG[A/T]TGTGGTGCAGGGTCT | 22992 |
rs558345203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67216334 | GAAATCAGCAAATTA[A/G]GATCTAAACCAACTT | 22992 |
rs558396858 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67240928 | CAGCTGCCACCCCCC[A/C]CACACACACCGACAC | 22992 |
rs558413031 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67139849 | GAGTAGCTGGGATTA[C/G]AGGCATGTGCTACCA | 22992 |
rs558417433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67230324 | ACCCCCATCTCAAAA[A/G]GTAACCAACAAAACA | 22992 |
rs558432635 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67224007 | GAAACCAGAATCAGG[G/T]TCTGGCTACTATGCA | 22992 |
rs558445942 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255671 | TTCTGCCCAGCACTC[A/G]TGCTTGTTCACATAA | 22992 |
rs558449302 | snp | C/T | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67193279 | ACAGGCGTGAGCCAC[C/T]GCACCTGGCCGAGAC | 22992 |
rs558503239 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | KDM2A | GRCh38.p7 | 11:67258252 | CACTTGCTTCTAGAA[A/G]TACAACGTTTACTTC | 22992 |
rs558513677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67201665 | CCCAGCTACTTGGGA[A/G]GCTGAAGCAGGAGAA | 22992 |
rs558549889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67201055 | AAAAATTAGCCGGGC[A/G]TGGTGGCGGGCGCTT | 22992 |
rs558573725 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67131107 | AGGCGGGCAGATTGC[C/T]TGAGGTCAGGAGTTC | 22992 |
rs558597909 | in-del | -/T | 0.375399 | 0.216275 | intron-variant | KDM2A | GRCh38.p7 | 11:67222059 | TTAACTCTGTCATTC[-/T]TTTTTTTTTTTTTTT | 22992 |
rs558624370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67207742 | AAAAGGGTTGTTTTC[A/G]GCTGGACGTTGGTAA | 22992 |
rs558639774 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67139030 | CTAATGGTATCTTAG[A/G]CACAGTATCCTTGAA | 22992 |
rs558665866 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67150340 | CTTTTCTCAAAAATG[A/T]GAAAAATTTACCACC | 22992 |
rs558675866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67205972 | AAAATATGATACTTC[C/T]CTTTTGTTTTTACTG | 22992 |
rs558684387 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67215811 | GGTGGGGCAGATGTA[C/G]TTTTTTCCATCAGTA | 22992 |
rs558696436 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67168050 | TATACTTCCTTAGGG[C/T]ATTTTAATTAAAATC | 22992 |
rs558698939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67248502 | TTTTTGTTTGGTTTG[A/G]TATGTTTTTCCTTTG | 22992 |
rs558706699 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67200315 | CCACCTCCTGGGTTC[A/G]CGCCATTCTCCTGTC | 22992 |
rs558716875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67223331 | CAGTCTTATAAGTTA[C/T]GAGTAAAAACTCAAA | 22992 |
rs558730357 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67184268 | GGAGGCTGAGGCAGG[A/C]GGGTCACTTGAGGTC | 22992 |
rs558745572 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67203717 | CTAGATTGTGCCACT[C/G]CACTCCAGCCTGGGT | 22992 |
rs558764657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67214696 | AGGCTGGTCTTAAAC[C/T]CCTGGGTTCAAGTGA | 22992 |
rs558767116 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67181135 | CAAGCGTTGCTTCTC[A/G]ATGTGCTCTCCATAT | 22992 |
rs558767367 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67219041 | TGGTGCTCCAGTAAA[C/T]GTTTATTATGTGCTA | 22992 |
rs558775060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67205552 | CACACCTCACCCTCC[C/T]GAGTAGCCGGGATTA | 22992 |
rs558780087 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67125879 | AACCGGGAGGCAGAG[G/T]TTGCAGTGAGCTGAG | 22992 |
rs558784966 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67175456 | CCAGCACACACACAC[A/G]TAATTTTCACACTGT | 22992 |
rs558860908 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255279 | GGAGTAGCAGATTGA[A/T]CTGAGGGGAAAGCAC | 22992 |
rs558873759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67130479 | TCCTGTCCTAAACTG[C/T]GCCTAGGTTTTGCTG | 22992 |
rs558887173 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67213183 | CTGCTTCATATCATG[C/T]ACAACTTTATGCATT | 22992 |
rs558894017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67184515 | CGCCTGTAATCCCAG[C/T]TACTCAGGAGGCTGA | 22992 |
rs558897264 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67204320 | TTTCATCACCCCAAA[C/G]AAACTCCATACCTTT | 22992 |
rs558919945 | in-del | -/TG | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67235492 | ATTTTTAGTAGAGAC[-/TG]GGCTTCTTCATGTTG | 22992 |
rs558933307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67138415 | ACCTACAAGGTTCTT[A/G]GTTCTAATAATTTAA | 22992 |
rs558935446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67225192 | ATTATTTTCACATCA[C/T]TCTAGTATACTGACT | 22992 |
rs558963347 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67222117 | TCTTGGGTGTTTCTC[A/G]CAGAGGGGGATTTGG | 22992 |
rs558982318 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67183910 | GTCCAGGAGTTTGAG[A/G]TCAGCCTGGGCAACA | 22992 |
rs559022937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67199597 | AAAGCCCTGATTCTC[C/T]TTAATTCTGTAAAGG | 22992 |
rs559051184 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255716 | CCAGCCTACCCGACT[G/T]ACTTGCTAGTCTCTA | 22992 |
rs559079258 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67145167 | GTGAGCCACCGTGCC[C/T]GACCATTCACATGGT | 22992 |
rs559111143 | snp | C/T | 2.58997e-05 | 0.0035985 | intron-variant | KDM2A | GRCh38.p7 | 11:67181431 | GGCTGGATGTAGTTG[C/T]AAAATGGCCTCGTTA | 22992 |
rs559122158 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67152262 | AGGTTGCAGTGAGCC[A/G]AGATTGCACCACTGC | 22992 |
rs559142495 | in-del | -/TTTA | 0.00279162 | 0.0372561 | intron-variant | KDM2A | GRCh38.p7 | 11:67151347 | ATACACACCACATAT[-/TTTA]TTTATTATTTTATTT | 22992 |
rs559149978 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67180582 | GGATTCCATGCGCAC[C/T]GTGCATCTTTGATCC | 22992 |
rs559159197 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67158572 | TGCCAGCATTTGGTG[G/T]TGTATTTTCAATTTT | 22992 |
rs559161410 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67142198 | TGCATCACCACGCCC[A/G]GCTAATTTCTGCATT | 22992 |
rs559187719 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67163900 | TATTTTTTGAGTATG[G/T]GCTAGATACTTTACA | 22992 |
rs559210794 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67151707 | GCCCCATAATTTTTT[A/T]CATTGACGATATATT | 22992 |
rs559244107 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67166259 | GTGTGATCTCGGCTC[A/C]CTGTAATCTCTCCCT | 22992 |
rs559248130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67172372 | GAAGATAAATTTGGG[A/G]GAGTATTGCCATCTT | 22992 |
rs559274923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67172168 | CTAATATATTTTTTT[C/T]TTGTAGAGGCAGTGG | 22992 |
rs559283669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67187734 | GCCCGCCACCACGCC[C/T]GGCTAAATTTTGTAT | 22992 |
rs559337801 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67148537 | CGGGCGTGGTGGCTC[A/G]TGCCTGTAATCCCAG | 22992 |
rs559362406 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67248026 | AGGTAATAATATCAG[C/T]CAACATTTTACAGTG | 22992 |
rs559365750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67164835 | AACTCCTGATCTCAA[A/G]TGATCTACCCACCTC | 22992 |
rs559372648 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67157614 | GCCAGACACAGTGGC[A/T]CGCGCCTGAAATCCC | 22992 |
rs559374388 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67147994 | CATTAGAGAGTCTTA[C/T]AGCAAATGTCTCTAG | 22992 |
rs559403907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67173294 | TGCGTGGCTAATTTC[A/G]TATTTTTAGTAGAGA | 22992 |
rs559415806 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67257109 | GTTTTATTTTGTTGT[C/G]TTTTTATAAAAGGGG | 22992 |
rs559424295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67227449 | GCCTTTTTTTCAAGT[A/G]TTTTGTGTCTTACTC | 22992 |
rs559433661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67134026 | AGAAAACTGACCTGT[C/T]CTTGTTGAAGTTGTA | 22992 |
rs559535984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67195510 | GGGACTGTGTTCTAA[A/G]CTGTCCAGTATGAAG | 22992 |
rs559551906 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67120697 | CCGGGGAGTCTAGAA[A/G]GGAAGGCGACGATTG | 22992 |
rs559552595 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67252214 | TGAAGGCAGGGTGAA[C/T]TGTGGATGTGCTGAG | 22992 |
rs559552618 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67214349 | AGCTGGGACTACGGG[C/T]GCCCGCCACCACGCC | 22992 |
rs559602008 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67235003 | TACAAAAATTAGCCA[G/T]GTGTCTTGGCGGGCG | 22992 |
rs559612163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67127561 | TCTTACATATAATTA[C/T]GAAATAGCTAAATCA | 22992 |
rs559647164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67142197 | GTGCATCACCACGCC[C/T]GGCTAATTTCTGCAT | 22992 |
rs559723486 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67146874 | GGATTTTATCTATTT[A/T]TTATTCCTTAACTGG | 22992 |
rs559741530 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67125446 | TTGGCCTCCCAACAA[C/G]TCATTTTTTGGGGGG | 22992 |
rs559758176 | snp | C/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67177617 | AGGCACAGTAACACA[C/G]ATGAGCTGTCATCTC | 22992 |
rs559758191 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67242282 | TGGGTGTGTGTATGT[A/G]TGTGTGTGTGTGTGT | 22992 |
rs559763788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67162004 | GTTGTCTTTGGTTAT[A/G]TCTGCCTAATCTGTA | 22992 |
rs559766472 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67138462 | GTGTGCTCCCCAGAC[A/C]ACATTACCTGGGAAC | 22992 |
rs559793769 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-3-prime | KDM2A, LOC107984341 | GRCh38.p7 | 11:67117630 | TGCTTCCAGGAGTCA[C/G]AGCTTAAAGAGTGGG | 22992 |
rs559819738 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67142120 | CTCCGCTCACTGCAA[A/C]CTCCACTTCCCAGGT | 22992 |
rs559822539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67225110 | TGGGATTACAGGTGT[A/G]AGCCATCACGCCCGG | 22992 |
rs559855890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67251018 | TCCTGGCCCTGCTCT[A/G]TACTTTCCCATGTCT | 22992 |
rs559877673 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67162701 | ATGAGCCACCGCGCC[C/T]GGCCTGCGATTTTTA | 22992 |
rs559891739 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67246988 | TGTTGCCCAGGCTAG[A/C]GTGCAGTGGCACGAT | 22992 |
rs559896452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67250025 | GGAGGTCCACCCTGT[C/T]GGTTCAGAGGGTTTG | 22992 |
rs559935673 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67189513 | AGGATTGCTTGAGCC[C/G]AGGATTTTGAGGCCA | 22992 |
rs559965429 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67170763 | TGCTGACTGGTCCCA[C/G]CACTACACCTTCTCT | 22992 |
rs559984865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67225717 | CAGGTTGCGGTGAGC[C/T]GAGATCACACCACTG | 22992 |
rs559989505 | snp | C/T | 4.47718e-05 | 0.00473116 | intron-variant | KDM2A | GRCh38.p7 | 11:67217929 | AGCCATTTTTTTCCT[C/T]AATGAAAAAGAAATT | 22992 |
rs560002160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67208041 | GTCTCAAAAATTTAA[A/G]ATAAAATGCGTTGTT | 22992 |
rs560067164 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67204064 | CCTCGGCCTCCCAAA[A/G]TGCTGAGATTACAGG | 22992 |
rs560154931 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67240444 | TTGTCTCAGTGAAGA[C/G]GCAGGAGAAACTGCC | 22992 |
rs560179282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67178660 | GGTCTTTTATGACTG[A/G]CTTTTTTTTTATTTG | 22992 |
rs560179991 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67140678 | GAGTTGCTTGAACCC[A/G]TGAGGCGGAGGTTGC | 22992 |
rs560216016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67186710 | GCCTAAAATCTAATA[C/T]TGAAACTTTGAGTGT | 22992 |
rs560239588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67223095 | TACTCAGGAGGCTGA[A/G]GCAGGAAAATCGCTT | 22992 |
rs560304716 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67186132 | ATGAAAGACAGGAGT[A/G]TAAACATCCAAACAG | 22992 |
rs560326870 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67123896 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCA | 22992 |
rs560339204 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67184174 | AGGCCTCTTCCCCTC[A/C]GCTGAACTGACTTCC | 22992 |
rs560367343 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67145989 | CCGTTTTTTGTTTTG[G/T]TTTTTTTTGTTTTTT | 22992 |
rs560371135 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67200727 | ACCCAGGCTGGTTTA[G/T]AACTCCTGGGCTCAA | 22992 |
rs560399927 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67236192 | CCGAAGTGCAGTGGC[A/G]TGATCTAGGCTCACT | 22992 |
rs560399939 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67257561 | TCCAAGCACCGGGGC[A/G]AAAAACCACAAAGGA | 22992 |
rs560415928 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67230592 | GATTGCATCACTGCA[C/G]TCCAGCCTGGGCAAA | 22992 |
rs560427004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67191608 | ATGATCATCTCAATT[A/G]ACACAGAGAAGGTAT | 22992 |
rs560479884 | in-del | -/AAAG | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67256360 | GCACTTTAAAAAAAA[-/AAAG]AAAGAAAGAAAGGTC | 22992 |
rs560484444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67160737 | GATAGTGCCATTGCA[C/T]GCCAGCCTGGGCAAA | 22992 |
rs560498411 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67190970 | TGGCTTTGGTGGTGA[A/T]TTCTACCAAACATTT | 22992 |
rs560563814 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67152430 | CAACAGAGCAAGAGA[A/C]CTCATCTCTACAAAA | 22992 |
rs560597102 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67128200 | TAGAGACAGGTTTTC[A/G]CTGTGTTGTCCAGGC | 22992 |
rs560608608 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67131393 | TCTCTCTTTTGAGGC[A/T]ACTTTAGTGTTTTCT | 22992 |
rs560629465 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67228688 | AAACCCTGTTGCGAA[-/A]AAAAAAAAAAAAAAA | 22992 |
rs560640950 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67167450 | TTGTTTGTGGTCAGG[A/G]TAAGTGTATCCCGAC | 22992 |
rs560667158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67170512 | CCGCCTCCTGGGTTC[A/G]CACCATTCTCCTGCC | 22992 |
rs560672833 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67240735 | CCCAAACCCCCTCTA[A/G]TGAAGGGTGGTGGCT | 22992 |
rs560674793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67199856 | AAGATAGCATCTAGG[A/G]TTTTCATAGCTAGAT | 22992 |
rs560687543 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67158900 | TTTTAAAAGTTGATT[C/G]TAAATTTTGAGTATT | 22992 |
rs560690616 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KDM2A | GRCh38.p7 | 11:67130597 | ATTGATACATTATGT[A/G]TATCATGTAGATAGA | 22992 |
rs560696246 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67123929 | TGATCCGCCTGTCTT[G/T]GCCTCCCAAAGTGCT | 22992 |
rs560701578 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67256108 | TCAGGGCAGTCAGGG[A/G]GTCCTGCTTAGAAGC | 22992 |
rs560706398 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67143944 | CCTTAAAAAAAACTA[-/T]TTTTTTTTTTTTTGT | 22992 |
rs560721276 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67237836 | CCTGTAGTCCCAGCT[A/C]CTCAGGAGGCTGAGG | 22992 |
rs560724613 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67130584 | ATTAAGTCAAGGAAT[C/T]GATACATTATGTATA | 22992 |
rs560730513 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67138817 | ACAGCCTGTGTTTCA[A/G]CTAGTTCTCCAGGTG | 22992 |
rs560739720 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67163872 | AAAAAAAAAAAAAAA[C/T]CACAGTTGCTGATAT | 22992 |
rs560753920 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67138645 | AATTAACCAGGTGTG[A/G]TGGTGTGCACCTGTA | 22992 |
rs560774486 | in-del | -/A | 0.312104 | 0.242163 | intron-variant | KDM2A | GRCh38.p7 | 11:67223192 | ATGAAACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 22992 |
rs560778317 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67161349 | TCTTCACTTTGGAGA[G/T]TATCTAGTGTATCAC | 22992 |
rs560778352 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67196774 | AGATGAACAGAGTTA[G/T]GGAGATGGATGGTGG | 22992 |
rs560808634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67247824 | CAAACCCAAAGAATT[A/G]GTGAAATAGGGTATT | 22992 |
rs560813055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67165994 | TACTGATGACTTAAC[A/G]GTTGCATCAATTATA | 22992 |
rs560845164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67208921 | CCCAAAAATAAAAAT[A/G]AACATTTTTATTATT | 22992 |
rs560939866 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | KDM2A | GRCh38.p7 | 11:67122691 | TTTATTTATTTATTT[A/T]TTGAGACAGAGTCTG | 22992 |
rs560947543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67136582 | TGAGATACTTGTAGG[A/G]TGGAGAATTCCTTGA | 22992 |
rs560947904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67128159 | AGATACATGCCACCA[C/T]ACCTGGCTTATTTTT | 22992 |
rs560951031 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67144807 | CTGGCCTCAAGTGAT[C/G]CTCCTGCTTCAGCCT | 22992 |
rs560977843 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67235897 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGCGCC | 22992 |
rs560988677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67175200 | TTATGAGATATGTTA[C/T]AGAAGCTTACTTTGA | 22992 |
rs560989964 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67151905 | ATGTACCACCACACC[A/G]GGCTAATTTTTTTAA | 22992 |
rs561005374 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67245119 | GCTAGGTATGCTACC[A/G]TGTAATCTTCTACCC | 22992 |
rs561011284 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67135510 | CCTCATGAGCTGGTT[A/G]TGGCCCTCAGCCTTA | 22992 |
rs561014826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67205638 | GTTTTGTGTGTGTGT[A/G]TGTTTAATTTTTTTT | 22992 |
rs561050423 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KDM2A | GRCh38.p7 | 11:67137254 | ACAGGTCAGATCAAA[C/T]AGGGCATTATCCTGA | 22992 |
rs561075196 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67213583 | GCCAAGATGGTGAAA[A/C]CCTGTCTCTACTAAA | 22992 |
rs561092289 | snp | A/C | 0.000140085 | 0.00836798 | intron-variant | KDM2A | GRCh38.p7 | 11:67254492 | ACTTGATCAGTAAAC[A/C]AGAATGACCTTGGGT | 22992 |
rs561153207 | in-del | -/TTTA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67122644 | TATTTTTTATTTATT[-/TTTA]TTTATTTATTTATTT | 22992 |
rs561157071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67181542 | GTATATGCTTTTCTT[C/T]TGATACACAAGTGTT | 22992 |
rs561166739 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67221137 | TAGAGAATGAGAGCT[G/T]ATTTTTTAGCAGAAT | 22992 |
rs561189711 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67143881 | AAGTGATCCGCCTGC[C/G]TCGGCCTCCCAAAGT | 22992 |
rs561203074 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67170825 | AGGTCGTCCTTGACA[A/G]TTTCTTCCGGTTACC | 22992 |
rs561237285 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KDM2A | GRCh38.p7 | 11:67174270 | CTCAAAAAAAAGAAA[A/G]AAACCGTTTCCTAAA | 22992 |
rs561241252 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67204692 | GAGATGGGGTTTCAC[C/T]GTGATAGCCAGGATG | 22992 |
rs561270214 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67228430 | GACACGCTGGTTCAC[A/G]CCTGTAATCCTAGCA | 22992 |
rs561293817 | snp | C/G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67236429 | GCCACCACGCCCAGC[C/G/T]ACAATTTGAGTTTTT | 22992 |
rs561297555 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67189816 | TGCACTCCAGCCGGG[A/G]CAACAAAGTGAGACT | 22992 |
rs561318984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67219821 | CTCCCAAAGTGCTGG[A/G]ATTACAGGTGTGAGC | 22992 |
rs561357015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67235985 | GAATAAAAAGGTAGG[A/G]CATGTAACAGTATGT | 22992 |
rs561357363 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67218861 | TGATCCACCCGCCTC[A/G]GCCTCCCAGAGTGCT | 22992 |
rs561374175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67148921 | GGTAGGGGCTGGTGG[C/T]GCATAGCTCAGCATT | 22992 |
rs561383179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67197825 | AACAATGCAACGGCT[A/G]GAGGCACCAACCCCC | 22992 |
rs561399820 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67155868 | TGATCCGCCTGCCTC[A/G]GCCTCCCAAAGTGCT | 22992 |
rs561400225 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67203360 | TGGAACTGAACCCAC[A/C]ATATCTCCAAGATAT | 22992 |
rs561421386 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67197137 | TTTAAAATAAAATAG[C/T]AATTATATCTAACCT | 22992 |
rs561446410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67226731 | CGTCTCAAAAAACAA[A/G]CGAAAATCAATCAGA | 22992 |
rs561448435 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67232717 | TTTAATTAATTAATT[A/T]ATTTATTTGAGACGG | 22992 |
rs561467717 | snp | C/G | 0.0023933 | 0.0345097 | utr-variant-5-prime, intron-variant | KDM2A | GRCh38.p7 | 11:67240133 | CTGAGCTGAAGGGCT[C/G]GAGAAGGAGCCCAGA | 22992 |
rs561483983 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67225935 | CTGGTCATGGTGGTG[C/T]ACACCTGTAATCCCA | 22992 |
rs561519501 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67149720 | TTACTAGGTATTAGA[A/G]TCTTTTTTTTTTTTT | 22992 |
rs561519982 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67133265 | CCACCACACTGCGCT[A/G]ATTTTGTGTTTTTTT | 22992 |
rs561537036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67188097 | CCTGTGCTCCTAGCC[A/G]CTTGGAAGGCTTGAG | 22992 |
rs561538085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67157507 | CCTAGCACTTTGGGA[A/G]GCCGAGGGGGGCGGA | 22992 |
rs561574887 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67187676 | GTCTCCTGGTTCAAG[C/T]GATTCTCCTGCCTCA | 22992 |
rs561604401 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67119596 | GCTCCCGCCCTGTCC[G/T]CCCCCCGGGGCCGGG | 22992 |
rs561608671 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67132724 | CCTGAACTCTTAAGG[-/C]AGTGGTTTTCAAAGT | 22992 |
rs561610872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67212427 | GCTGCCATTCCAGCA[A/G]TAACTGAGAGGTAGA | 22992 |
rs561630946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67171113 | CTTAAACATTTAGAC[C/T]CCTTTGTGCCTTTTG | 22992 |
rs561644801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67163804 | GAGGTTGCAGTGAGC[C/T]GAGATAGCACCACTG | 22992 |
rs561736776 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67120647 | TTGTGCACATCTTGT[G/T]TTGGGGTGGAGGGTA | 22992 |
rs561772728 | in-del | -/GGAGGGAG | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67256211 | TCTGCGCGTGTGTGT[-/GGAGGGAG]GGAGGGAGGGGAGCA | 22992 |
rs561787825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67171977 | AATTACTATAGTTTT[A/G]TAGTGAGTTCTTCAC | 22992 |
rs561789831 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67197481 | CTCTGCCCAGCCAGT[C/G]ACTAACTTTCTATCC | 22992 |
rs561805283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67134653 | GGGATTACAGGTATG[C/T]GTCGCCACGCCCAGC | 22992 |
rs561824658 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67180418 | TCTCCTATATTAGAA[A/G]TAATCTTTTTATTAG | 22992 |
rs561856729 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67161967 | CAACTCAGTTTTCAG[A/T]ATTTATATTATGCTC | 22992 |
rs561857907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67234167 | TCTCAGAAAAGATAT[A/G]GCAAGCTTAGAGCTT | 22992 |
rs561867520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67133969 | AGTGCTAGGATTAGA[A/G]GCGTGAGCCACCATG | 22992 |
rs561921559 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67147348 | GAGATTGAGACCATC[C/G]TGGCTAACACGGTGA | 22992 |
rs561928772 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | KDM2A | GRCh38.p7 | 11:67141394 | GTTATTGGCCGGGCG[C/T]GGTGGCTCACGCCTG | 22992 |
rs561939063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67243200 | GATGGCTTTTGGTGC[A/G]TTAATACAAACTGAC | 22992 |
rs561943591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67170035 | CGCTGTGATTACTGG[C/T]GTGAGTCACCATGCC | 22992 |
rs561979807 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67169384 | TCTTTCTTTTTCTTT[C/T]TTTTTTTTTTTTGAG | 22992 |
rs562006907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67252095 | TCAGTTCTGGTCTGG[C/T]CTGGCTAGAAAATGT | 22992 |
rs562016227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67155559 | CCCTCCTGCCTCAGC[C/T]TCTCAGGTTGCTGGG | 22992 |
rs562024462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67208676 | CTCGGGAGGCTGAGG[C/T]ATGAGAATCGCTTGA | 22992 |
rs562045455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67251244 | CCTCTCCATTCAGTG[A/G]GAGAAGTGGGCATGC | 22992 |
rs562070589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67202598 | TAACATGGTGAAACC[C/T]CGTCTCTACTAAAAA | 22992 |
rs562086161 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67132495 | TCAACTATTATTGGC[A/C]AGGCTGGTCTGGAAC | 22992 |
rs562095688 | snp | A/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185471 | CTGTCTCTACTGAAA[A/T]TACAAAACTTAACTG | 22992 |
rs562100965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67156164 | GAGGCAGAAGAATCA[C/T]TTGAACCCAGGAGGT | 22992 |
rs562146197 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67139991 | CTATAGGCGTGAGCC[A/C]CCGCACCTGGCCTAC | 22992 |
rs562157834 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67209818 | GTAATTCCAGCACTT[C/T]GGGAGGCTGAGGTGG | 22992 |
rs562209132 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67139488 | GACCTCTGGTGATTC[A/G]CCCACCTCGGCCCCC | 22992 |
rs562212415 | snp | C/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185738 | GAGATAATTAGGCTA[C/T]AGGGACTCCACTCTC | 22992 |
rs562224765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67125381 | AGGTGGGGTTTTGCC[A/G]TGTTCCCAAGGCTAG | 22992 |
rs562235535 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67217098 | AATACAAAAATTAGC[A/T]GGGTGTGGTGGCGCA | 22992 |
rs562264963 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-3-prime | KDM2A, LOC107984341 | GRCh38.p7 | 11:67117423 | CAAGTTGTGCATGCA[G/T]AAAAACCTTCTGTGG | 22992 |
rs562274508 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67225042 | GGGTTTCAGCAGGCT[A/G]GTCTCGAACTCTTGA | 22992 |
rs562323993 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67125861 | AGTCAGGAGAATCAC[C/T]TGAACCGGGAGGCAG | 22992 |
rs562334676 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67124494 | TTTTTTTGTATTTTT[A/G]GTTGAGACGGGGTTT | 22992 |
rs562337188 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67197857 | GCAAGTCAGAAATCT[A/G]CATATAAATTGGAAT | 22992 |
rs562340330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67178547 | TCACTTCTCCCATTC[C/T]TCATTTTCTCTAGCC | 22992 |
rs562341353 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67235798 | CTAATTTTTGTATTT[G/T]TAGTAGAGACGGGGT | 22992 |
rs562364090 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67224377 | TTTTGGGAGTTTGAA[A/G]CGAAGGATCACTTAA | 22992 |
rs562369226 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67240509 | CGTGTTGCTTGAGCC[G/T]TCATTGCACTTGTTC | 22992 |
rs562370547 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67224908 | GTGCAGTGGTGTGAT[C/G]TCAGCTCACTGCAAC | 22992 |
rs562380448 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67232830 | CTCGTGCCTCAGCCT[C/T]CTGAGTAGCTGAGAT | 22992 |
rs562450922 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67164890 | ATGTGTGAGCACCGC[A/G]CCTGGCCTGCTATTG | 22992 |
rs562489256 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67133549 | CTTGGATTACAGGCT[C/T]CCACCACCACGCCCG | 22992 |
rs562497986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67193498 | TAGTTTTAAAAGTTA[A/G]TACACATAAAGTGCT | 22992 |
rs562552143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67223036 | TGTCTCTACTAAAAA[C/T]ACAAAATTAGCCAGG | 22992 |
rs562569194 | in-del | -/AG | | | intron-variant | KDM2A | GRCh38.p7 | 11:67157931 | CCCATCGCAAAAGAA[-/AG]AGAGAGATACATTGT | 22992 |
rs562589847 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67192824 | TTGAGAGTTTAGACG[G/T]TATAAGCCTAGAAGT | 22992 |
rs562589900 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67201173 | CACTACAGCCTGGGC[A/G]ACTGAGCAAGACTCT | 22992 |
rs562628531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67200699 | TTTGGTAGAGACACA[A/G]TTTGACCCTGTTACC | 22992 |
rs562637441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67229898 | AAAATACATCTAGGC[C/T]GGGTGTGGTGGCTCA | 22992 |
rs562702700 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67191528 | TTATTCCTGGAATAG[A/G]TGATTTGACATGTGA | 22992 |
rs562725305 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67124551 | CTCCTGACCTCAGAT[G/T]ATCACCCACCTCGGC | 22992 |
rs562757533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67123819 | GTAGCTGAGATTACA[A/G]GTGCCTACCACCACA | 22992 |
rs562775019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67152897 | AGACTATAGGATTAC[A/G]GTGCCAGAGTGTGTG | 22992 |
rs562778220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67176354 | AGATTCAGGTGCTAT[A/G]TAATCAATTCTAGAT | 22992 |
rs562784984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206413 | ACTCCAGCCTGGGTG[A/G]CACAGCGAGACTGTC | 22992 |
rs562815186 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67159402 | CATTGTATAGATTAA[-/T]TTGTTTTCCTAAGCT | 22992 |
rs562822584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67130573 | TGGTTTTGGTTATTA[A/G]GTCAAGGAATTGATA | 22992 |
rs562825050 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67199040 | CGCCTTGGCCTCCCC[A/G]AAGTGCTGAGATTAC | 22992 |
rs562877622 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67237599 | ACCTTACCCAACCAA[C/T]TCAGCTTTTTGTTTG | 22992 |
rs562914866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67198284 | CCCAGAGTATGAGCG[C/T]ACCTCATTTTATTGC | 22992 |
rs562977471 | in-del | -/GA | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67248242 | GGATAAAGGAAGCTT[-/GA]GAGACAGGCTTTTAA | 22992 |
rs562979606 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67122885 | TTTCACTGTGTTAGC[A/C]AGGATGGTCTCGATC | 22992 |
rs563009943 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67157775 | AAAAACTTGCATTAG[C/T]GTTGTACATTTGTTA | 22992 |
rs563027782 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67253385 | TTGTTCACTTTGCTC[A/G]GATCGTTACGGCTCT | 22992 |
rs563041832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67129798 | TGCCTGTAATCCCAG[C/T]TACCCAGGAGGCTGA | 22992 |
rs563056188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67183427 | ATATTGTTAAAAATA[C/T]AGACTCTCAGAGAGG | 22992 |
rs563077034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67137887 | ACTGCAACCTCTGCC[C/T]CCCAGGTTCAAGTGA | 22992 |
rs563106766 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67205566 | CCGAGTAGCCGGGAT[A/T]ACGGGCACGCACCAC | 22992 |
rs563113029 | in-del | -/AG | | | intron-variant | KDM2A | GRCh38.p7 | 11:67249794 | TTTCCACCATGAAAC[-/AG]AAATACGTCTCTTGG | 22992 |
rs563120995 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67158759 | TGCCCAAAGTGCTCG[C/T]ATTATAGGCGTGAAC | 22992 |
rs563122277 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67236709 | TAAAATATCTGTGAG[A/T]TTGTTGTTAAAATTA | 22992 |
rs563141961 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67174079 | CCTGGTCAGCATGTC[A/G]AAACCTTGTCTCTTC | 22992 |
rs563156780 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67187516 | TATACTTATATCAGA[C/T]AAAACAGACATTTAT | 22992 |
rs563183509 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67189707 | TAGCCAGGCATGATG[A/G]TGGACACCTGTAGTC | 22992 |
rs563195305 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67165617 | AGCTTCCTGATGAGA[A/G]GAATGTAGCAAAGCT | 22992 |
rs563203234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67143980 | GGAGTCTCCCTCTGT[C/T]GCCCAGACTGGCGTG | 22992 |
rs563260705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67254685 | GTGCTTGTTGTCATA[C/T]GGTGATGGGAGTGAG | 22992 |
rs563268667 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | KDM2A | GRCh38.p7 | 11:67225087 | CTTGCCTTGGCCTCC[C/G]AAAGCGCTGGGATTA | 22992 |
rs563277551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67150928 | TTCAGTCTAAACCTA[A/G]TGTTGAAGGCCAAAG | 22992 |
rs563344803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67220387 | TCATTTTTATGCTCA[C/T]AGAATAATTTGGTGT | 22992 |
rs563348132 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67143246 | TCGTGACCTCAGGTG[A/T]TCCTCCCGCCTCCGC | 22992 |
rs563354939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67128702 | TCTGTTGTTTTATTT[C/T]GCTGAGCATTAATCA | 22992 |
rs563367575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67158121 | TTTCCTCTCCCCCAT[A/G]CACCAGCAACTACGG | 22992 |
rs563378166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67213479 | TTAAAAGATTCCTGG[C/T]CGGGCATGGTAGCTC | 22992 |
rs563391570 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67131216 | GTAGTCCCAGCTACT[C/G]GGGAGGCTGAGGTGG | 22992 |
rs563399874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67149452 | AACAAGCCAGTTTTA[C/T]GCCTTTTAAATCTGA | 22992 |
rs563410014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67142327 | CAGGCATGAGCCACC[A/G]CGCCCACTGTATATC | 22992 |
rs563431745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67235910 | GGCGTGAGCCACTGC[A/G]CCCGGCCAAGATATC | 22992 |
rs563437587 | in-del | -/TTTTG | 0.0737376 | 0.17729 | intron-variant | KDM2A | GRCh38.p7 | 11:67235604 | CGCGCCCGGCTGCTT[-/TTTTG]TTTTGTTTTGTTTTG | 22992 |
rs563467951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67220944 | TCATGATTAGGTGTT[C/T]ATGCACGTATGTGAA | 22992 |
rs563481806 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67228413 | GAAGGATGATCAAGC[C/T]GGACACGCTGGTTCA | 22992 |
rs563489775 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67121460 | TGATTAAAACTTTTC[A/G]GGTGACTTTTCTGTG | 22992 |
rs563536016 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67214739 | GGCCTTCCAAAGCTC[G/T]GGGATTGCAGGTGTG | 22992 |
rs563565707 | in-del | -/GCAGGATTGCTGC | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67239316 | CACGGTGGAACTGCT[-/GCAGGATTGCTGC]GCAGACATTTCTAGT | 22992 |
rs563570388 | snp | C/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206710 | CCACTGCACTCCAGC[C/T]TGAGCGACAGAGCGA | 22992 |
rs563574744 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67251970 | TGTCTCTCTTCCCCT[A/G]CCAACCAGGCTGGGG | 22992 |
rs563593624 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67148672 | TGGGCGTGGTGGTGG[A/G]TGCCTGTAATCCCAG | 22992 |
rs563608005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67235176 | GAAAAAAGAAAGGAA[A/G]TATTGCCTTACCGGT | 22992 |
rs563617507 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-3-prime | KDM2A, LOC107984341 | GRCh38.p7 | 11:67117379 | AAGGATGTTGTGAAA[C/T]AAAGCAGAGAATGTC | 22992 |
rs563621015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67181500 | AAACAATAGTAATTG[A/G]AAATAATTTCCCACT | 22992 |
rs563634591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67120313 | CTGCCTCTAACTGCT[C/T]TGCAAACTGTGTCAT | 22992 |
rs563635809 | in-del | -/T | 0.134119 | 0.221521 | intron-variant | KDM2A | GRCh38.p7 | 11:67131412 | TAGTGTTTTCTTTTC[-/T]TTTTTTTTTTTTTTT | 22992 |
rs563643179 | in-del | -/TTTC | | | intron-variant | KDM2A | GRCh38.p7 | 11:67154424 | TACCTATTCTGGGTG[-/TTTC]TTTCTTTCTTTCTTT | 22992 |
rs563643303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67135354 | CAAGCGTGAGCCACC[A/G]CGCCCAGCACAGATT | 22992 |
rs563657381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67189229 | CCAACCACAATGGGA[C/T]GAAGTTAAAAATCAA | 22992 |
rs563668486 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67226594 | GGGCGTGGTGGCGGG[C/T]GCTTGTAGTACCAGC | 22992 |
rs563681826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67253150 | AGAGGAAATTTGAGT[C/T]AGATGTTACTTTGGT | 22992 |
rs563697375 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67119311 | GCTGCTTCAGCGGCT[C/G]CTCCTGTGTGAGGGA | 22992 |
rs563724548 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67244341 | TTATTGAAGTGTCTG[C/T]TATCTACCAGTTCGT | 22992 |
rs563756157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67196275 | CACCTCCAGTTCTTC[A/G]TGTCAGCCAGATGGC | 22992 |
rs563786687 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67235893 | AAAGTGCTGGGATTA[C/T]AGGCGTGAGCCACTG | 22992 |
rs563800627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67156526 | ATCGAGACCATCCTG[A/G]CTAACACAGTGAAAC | 22992 |
rs563812620 | in-del | -/AAAAT | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67178414 | CATCTCAGAAAATAA[-/AAAAT]AAAATAAAGTGTACA | 22992 |
rs563820063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67210121 | CCTGTAATCCTAGCA[C/T]TTGGGGAGGCCGAAG | 22992 |
rs563823564 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67217073 | ATGGTGAAACCCCGT[C/T]TCTACTAAAAATACA | 22992 |
rs563834388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67162979 | CCTCCCAAAGCGTTG[A/G]GATTATAGGCTTGAG | 22992 |
rs563842786 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67203310 | AAAGTTTTGTATGAC[G/T]TGCTTACTGGAATAG | 22992 |
rs563978447 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67171859 | ACTGTAAGTGTAAGA[C/G]TTTATGCCTGCATTC | 22992 |
rs564009521 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67126119 | AACGTGGTGACGCAT[G/T]CCTGTAATCCCAGCT | 22992 |
rs564022968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67202000 | TTTGTGGTACATGGG[A/G]GGAGGTCAAAATATC | 22992 |
rs564029954 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67225498 | ACAATTGGCCAGTCA[C/T]GCTGGCTCACGCCTG | 22992 |
rs564066089 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67170960 | CCACATCAATTACTA[G/T]CTTTGTAACCTGGGC | 22992 |
rs564068379 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67193820 | AAGCTGAGACCATGT[C/T]GTTGTATTCCAGCCT | 22992 |
rs564104843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67208643 | AAGCATGGTTGCATG[C/T]GCCTGTAATTCCAGC | 22992 |
rs564110669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67201353 | TGCCATTAAGAACAT[A/G]TTTATGGCCAGGCAT | 22992 |
rs564129952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67126621 | GCTCAGACAGGAGAA[C/T]TGCTTGAACTCGGGA | 22992 |
rs564148929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67241292 | CTTCACCCCCACGCT[A/G]TATGGTACTAACAGA | 22992 |
rs564171594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67194586 | CAATGTGGCATAACA[C/T]TTTGTGCATTACATA | 22992 |
rs564185940 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67251069 | CTGATTTGCGGGATA[C/G]ATTTGTAGTCTGTGA | 22992 |
rs564190899 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67133880 | TGTATTTTTAGTAGA[C/G]ACAGGGTTTCACCAT | 22992 |
rs564212571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67141289 | TTGTAATGACCAAGT[C/T]AGAGTATTTGGGGCA | 22992 |
rs564230432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67187636 | CTGGTGTGCAGTGGT[A/G]CAGTCTCGACTCACT | 22992 |
rs564283549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67251886 | TATTTCTCTGTCTAG[A/G]GCTAATAGGACTGCT | 22992 |
rs564297275 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67201051 | GAAAAAAAATTAGCC[A/G]GGCGTGGTGGCGGGC | 22992 |
rs564329419 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67147271 | CACTGGGCCGGGTGC[A/G]GTGGCTCAAGCCTGT | 22992 |
rs564334192 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67168347 | TGTTAGTTGTTCTTC[C/G]TACTGGGCTTCAATA | 22992 |
rs564337985 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67182738 | TGGTTTCACCATGTT[A/G]GCTAGGCTGGTCTTG | 22992 |
rs564374641 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67217178 | ACCCAGGAGGTGGAG[A/G]TTACGGTGAGCCAAG | 22992 |
rs564395482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67161313 | CTATAGAAATTGTAT[C/T]CACGTGAAACCTTTG | 22992 |
rs564415251 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67216562 | TTTTTTCTCTAACTT[G/T]CAGTGAATGCATTTG | 22992 |
rs564417798 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67146608 | CCACCTCCCAGACTT[A/C]AGCAATCCTCCTGCC | 22992 |
rs564452576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67124159 | CAGGTGCCCACCACC[A/G]CACCCAGCTAATTTT | 22992 |
rs564461143 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | KDM2A | GRCh38.p7 | 11:67258548 | TCAGGTAATCTGCCC[A/G]CCTCCACCTCCCAGA | 22992 |
rs564489697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67161842 | GAACTATATCATGTG[C/T]GATGATAATGCTCTC | 22992 |
rs564547020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67145836 | CCTCTCTAACTCTGC[C/T]TTTCAGGTTTCAGGT | 22992 |
rs564608321 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67145441 | GTGCCAGTGAGCTGA[G/T]ATTGTGCCACTTCAC | 22992 |
rs564617427 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67152033 | TTAAAATTAATTTCC[C/T]GCCGGGTGCAGTGGC | 22992 |
rs564626537 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67125340 | CCTGTGCCACCATGC[C/G]TGGTTAATTTTTGTA | 22992 |
rs564646187 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67256397 | ATTTCTTTTGGGTCA[A/G]TATTTTTAAGTGTGT | 22992 |
rs564650235 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67184787 | AGACGTAAGAAAACT[G/T]AAGTGTATACCTCAG | 22992 |
rs564687157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67231501 | CCTATCATGCCACCT[A/G]TTTCTCTTGCTGATC | 22992 |
rs564691106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67124533 | TGGCAGGCTGGTGTC[A/G]AACTCCTGACCTCAG | 22992 |
rs564700678 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67221800 | CAAAGCCGGGTGTGG[A/T]GGTGCATGCCTGTAA | 22992 |
rs564718741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67223734 | TTTTAAACTGTCATT[A/G]TTACTCAGCTTTCAA | 22992 |
rs564723947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67230720 | TATTGTACTGTTCAG[C/T]TGTTATCGTAGGATG | 22992 |
rs564809586 | in-del | -/TTTGT | 0.0721586 | 0.175706 | intron-variant | KDM2A | GRCh38.p7 | 11:67198764 | TGATCAGTAGTTTGT[-/TTTGT]TTTGTTTTGTTTTGT | 22992 |
rs564826527 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67133771 | CAGTGGCGCCATCTC[A/G]GCTTACTATAACTTC | 22992 |
rs564858134 | in-del | -/CTT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67253230 | GACAGGAAGTCACTC[-/CTT]CTTGTATTGCTCTGG | 22992 |
rs564861771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67229827 | GTGAGCCGAGATCAC[A/G]CCACTGCACTCCAGC | 22992 |
rs564882968 | in-del | -/A | 0.264632 | 0.249571 | intron-variant | KDM2A | GRCh38.p7 | 11:67157747 | CAAGACTCCGTCTCC[-/A]AAAAAAAAAAAAAAA | 22992 |
rs564905134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67138714 | TGAACCTGGGAGGTG[A/G]AGGTTACAGCGAGCC | 22992 |
rs564914588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67146632 | TCCTGCCTCAGCCCC[A/G]CAAGTACCAGGGACT | 22992 |
rs564941853 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67191787 | GAACAGCGTAAAGGC[A/G]CCTGCTTTTACTGCC | 22992 |
rs564950476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206896 | CCATCCTGGTGTCTT[C/T]ATCATTCTATAAATA | 22992 |
rs564955362 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67229366 | TTTCAAGTTTCCCCA[A/G]CATCTATCAGAGAAA | 22992 |
rs564957139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67248007 | AGTTCCTGAGGGAAA[A/G]TGAAGGTAATAATAT | 22992 |
rs564957931 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67199961 | CCAAATTTAACATTC[A/C]AAAAAAAGCTTATTT | 22992 |
rs564958527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67129747 | TCAAAAAAAAAAAAA[A/G]AAAGAAAAAGAAAAA | 22992 |
rs564989038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67236677 | ACTAAATTTATGGAA[A/G]CCTATTTTCTCCTCT | 22992 |
rs564993682 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67256316 | GGCCTGTCCAAAGAT[C/T]CTCTCTCTAGGGCAG | 22992 |
rs565037412 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206325 | ATTCCCAGCTACTTG[C/G]GAGGCTGAGGCACAA | 22992 |
rs565080934 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67236063 | ATTGCAGAGGAATCT[A/G]AAAGGGTACATCCCA | 22992 |
rs565146943 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67177292 | ACTACTACTAGTAAT[A/G]AAACTAAGCTTAGTC | 22992 |
rs565156501 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67159041 | TCCAGTTTATTAATT[A/T]TTTTTTTCATGGATC | 22992 |
rs565160366 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KDM2A | GRCh38.p7 | 11:67143929 | GAGCCACTGTGCCTG[A/G]CCTTAAAAAAAACTA | 22992 |
rs565181431 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KDM2A | GRCh38.p7 | 11:67176226 | TGCTTTCCTCTGGTA[C/T]GTAATAGTCAAGTTT | 22992 |
rs565189444 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67173882 | AACTAATTTAAACAA[-/T]TTTTTTTTTTTATAA | 22992 |
rs565190524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67228591 | TCAGGAGGCTGAGGT[A/G]GGAGGATCACTGGAA | 22992 |
rs565193993 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67166723 | AATATGGTGACCTCC[C/G]AGCAACTGGGGACCA | 22992 |
rs565214428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67221884 | AGGTTGCAGTGAGCT[A/G]TGTTGGTGCCACTGT | 22992 |
rs565225505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67205069 | GTTTAGTTTATTGAG[A/G]AACTGCAAATCCAAT | 22992 |
rs565257670 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67190757 | CAGAGCGAGACTCTT[A/T]AAAAAAAAAAATACT | 22992 |
rs565273988 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67246626 | TCAGCCTCAGAGATT[A/G]AGTCCAGCATGGGCC | 22992 |
rs565276608 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67175334 | TTTGGGAGGCCAAGG[C/T]TGGAGGATCACTTGA | 22992 |
rs565278831 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67211312 | TGTAAGTAACCACCA[C/T]AGTCAAAATATAGAA | 22992 |
rs565298227 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67198815 | ACGGAGTCTCACTCT[G/T]TTGCCCAGGCTGGAA | 22992 |
rs565314152 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67183316 | TCTTTTATTAAAGAG[C/T]CTCCAGGACAGTAAT | 22992 |
rs565315956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67205820 | TTATTTTCTCTCCCT[C/T]CCTTGACCACCATTT | 22992 |
rs565347755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67203499 | ATATTAATATATTTT[C/T]ATATAATATATAATA | 22992 |
rs565378177 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67159726 | AGGTACTGGGAAGAC[A/G]GTGGTGAAAAAGAGA | 22992 |
rs565382923 | snp | C/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185601 | CACCATTGACTCCCT[C/T]GCACTCTAGCCTTGG | 22992 |
rs565401964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67182289 | GTGCTGCATTTGGAA[A/G]CTTGCCTAAGACTTG | 22992 |
rs565434245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67203025 | AAAAAAAAAGAAAAA[C/T]GGTTTACACTTCAGC | 22992 |
rs565484601 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67138088 | GGCGTGAACCACCGC[A/G]CCTGGCCAAACTATA | 22992 |
rs565522816 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67198073 | ATCTTTTCATCTTCA[C/T]GATGAGTAGGCTAAG | 22992 |
rs565532508 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67179523 | GACCTCAGGTGATCC[A/G]CCTGCCTCTGCTTCC | 22992 |
rs565534409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67142062 | ATTCATTTTTGAGAC[A/G]GAGTCTTGCTGTGTC | 22992 |
rs565566882 | snp | A/G | 0.000149243 | 0.00863707 | intron-variant | KDM2A | GRCh38.p7 | 11:67252561 | GGCAAAAAATGATAA[A/G]GTGTGATCCCTGTAC | 22992 |
rs565569259 | snp | A/G | 0.000165706 | 0.00910084 | intron-variant | KDM2A | GRCh38.p7 | 11:67215810 | TGGTGGGGCAGATGT[A/G]CTTTTTTCCATCAGT | 22992 |
rs565592743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67217490 | CTCTTCTCTCCGAGT[C/T]CTGGATGGTGTATAG | 22992 |
rs565618238 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67157905 | GTCTAGCCTGGGCAA[C/T]ATAGTGAGACCCCAT | 22992 |
rs565620291 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67149810 | ACTGCAACCTCGGCC[C/T]CCCAGGTTCAAGTGA | 22992 |
rs565659368 | in-del | -/TTATTTAT | 0.0372196 | 0.131242 | intron-variant | KDM2A | GRCh38.p7 | 11:67223389 | TTCCTTTTTTCTTTC[-/TTATTTAT]TTATTTATTTATTTA | 22992 |
rs565659651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67179508 | TAATCTCGAACTCCC[A/G]ACCTCAGGTGATCCG | 22992 |
rs565660555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67253339 | GACTAAAAGATTAGG[C/T]ATAGTCCTTCTCTCC | 22992 |
rs565694942 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67136001 | GTAACTATAATTAAC[A/G]TTACTAGTGTGTTTG | 22992 |
rs565696956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67178956 | CGATAACTTTGTTTA[A/G]CTTTTTGAGAAACTT | 22992 |
rs565748474 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KDM2A | GRCh38.p7 | 11:67157263 | GCTGGCAGTGAGCCA[A/G]AATCGCGCCACTGCA | 22992 |
rs565750290 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67148473 | GTAAAACTCAAATAA[G/T]AGGTATCAATCATAT | 22992 |
rs565779891 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67151006 | CCCCCCTTGCATGCA[A/G]TAGAGATGTGATATT | 22992 |
rs565785452 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67156643 | AGAATGGCGTGAACC[A/C]GGGAGGCTGAGCTTG | 22992 |
rs565818514 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, missense | KDM2A, LOC107984341 | GRCh38.p7 | 11:67118142 | CCCGGGCCGCCGGGG[A/G]CACCGGCGCGGCGGA | 22992 |
rs565821425 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | KDM2A | GRCh38.p7 | 11:67186394 | AACTGTCAACCAAGC[A/T]TCCTATATCTGGCAA | 22992 |
rs565832184 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67249174 | GATTTTTGAAGTTGA[C/G]TAGGGCCAAAGTTCT | 22992 |
rs565856510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67170493 | TCTCAGCTCACTGCA[A/G]GCTCCGCCTCCTGGG | 22992 |
rs565877361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67147398 | ATAAAGAAAATTAGC[C/T]GGGTGTGGTGGCGGG | 22992 |
rs565900476 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67119871 | CCCGGTCTCCAAAGC[C/T]AGAAGAGAAGGTTTG | 22992 |
rs565901584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67171289 | TCCTAGTCAGGACAG[A/G]CGAGGCCGAGTCTGA | 22992 |
rs565922074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67226011 | TGGAGGTTGCAGTGA[A/G]CCAAGATTGCACCAT | 22992 |
rs565980533 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67223124 | TTGAACCTGGGAGGC[A/G]GAGGTTGCAGTGAGC | 22992 |
rs566024052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67126302 | GTCTTTTGCCAGTTA[C/T]GGTGACTCACACCTA | 22992 |
rs566035420 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67161432 | AGACAGTAGATTAGG[A/C]AAATTAGTATGTTGT | 22992 |
rs566039162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67154438 | GTTTCTTTCTTTCTT[C/T]CTTTCTTTTTTAAGA | 22992 |
rs566075301 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67140317 | GCTGCAGTGAGCTTT[A/G]ATTACGCCACTGCAC | 22992 |
rs566087402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67133350 | CAAGTGATCCACCCG[C/T]CTTGGCCTCCCAAAG | 22992 |
rs566121131 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67146856 | TTCCTCCCTCACTTT[C/T]GTGGATTTTATCTAT | 22992 |
rs566135825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67140932 | TTTATTAGGTAGAAC[C/T]AGTTTAAAAAACGCT | 22992 |
rs566152141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67194687 | ATAAAAATGTAGGTG[A/G]TATTAAACCACAAGC | 22992 |
rs566164684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67251514 | TACTCTAGGATATAT[C/T]CTTTTTATCTGGGTC | 22992 |
rs566216783 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67125007 | GGGCTACAGGCGCCC[A/G]CCGCCACACCCGGCT | 22992 |
rs566264729 | snp | G/T | 1.69344e-05 | 0.00290979 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67250175 | GCCTCTCACGCCCCC[G/T]CCTCATTCACCCACT | 22992 |
rs566280304 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67124205 | GATGGAGTTTCACCA[C/T]GTTGGCCAGGCTGGT | 22992 |
rs566311235 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67239545 | AAGCAGGCAGTGTGC[A/C]GGAGAGAGAAGATAA | 22992 |
rs566341160 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67131020 | CCATCCAACGTCTCT[C/T]GTGTACTTTATACAG | 22992 |
rs566375671 | snp | C/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67238238 | TTTGGAAACTTACTG[C/G]GAGTGAGTTTCCTAG | 22992 |
rs566395090 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67223945 | ATTAATTTTACTTCC[A/G]TGTAAGAGAGTCATT | 22992 |
rs566396523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67249465 | GATACGGTTCCTAGT[A/G]GAACATGTTTACTGG | 22992 |
rs566403672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67216696 | GAGGCCAAGGCGGGC[A/G]GATCAGCTGAGGTCA | 22992 |
rs566429394 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67162652 | CTCAAGTGATCCGCC[C/T]GCCTCGGCCTCCCAA | 22992 |
rs566431037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67248438 | GGGGGATTGCTACAC[A/G]TTTGCCTTTGCATTA | 22992 |
rs566458035 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67144547 | GTGAGCCACCGTGCC[C/T]GGCCCCAACATTTTT | 22992 |
rs566460100 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67177334 | AACTTTATATACTTT[G/T]GAACATTTTCTAATT | 22992 |
rs566475281 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67224465 | TTAACCCCTTTCTTT[C/T]TTTTTTTTTTTTTTT | 22992 |
rs566484606 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67230945 | ACAAAAAAAAAAAGT[G/T]TTTTGGTTTTTTTTT | 22992 |
rs566490347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67216297 | AGTGGAAGGGAACAC[A/G]AATTTTGGATAGATT | 22992 |
rs566517499 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67195679 | TGCAGTCTGTATAAC[C/T]TTGGGTTTTAAATTC | 22992 |
rs566537616 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67168232 | ACACAGTCTGTATCT[A/G]TGGTCTTTGGAACTT | 22992 |
rs566615499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67176890 | TGAATAGTGAGTAAA[C/T]GCGAGGGCCTAAGAC | 22992 |
rs566615996 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67215553 | GTCTTGAATGATTAA[A/T]AAGATGAATTATTTA | 22992 |
rs566621655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185347 | TAGGTTAAATGTTAT[C/T]CCTGCCAGGTGTGGT | 22992 |
rs566627440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67138984 | CTTCATATTTCCTGC[C/T]AGTTGAATTTGCTGA | 22992 |
rs566655713 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67198642 | GTGAACCCGGAAGGC[A/G]GAGGTTGCAGTGAGC | 22992 |
rs566669797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67139536 | AGGCGTGAGCCACTG[C/T]ACCCAGCCTCTTTTT | 22992 |
rs566687691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67145613 | CCCTAACGTTATACT[A/G]CTAAGCAGTAGAACA | 22992 |
rs566705888 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67201792 | AAAAAAAAAAAAAAA[A/G]AAAAAAAAAAAAATT | 22992 |
rs566711638 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67192907 | TACCAGTTTACACTT[C/T]GTTGAGTCAAGTAGG | 22992 |
rs566726769 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67200220 | ATTGTTTGTGTGGTT[G/T]TTTTTTTTCTTTTTA | 22992 |
rs566741113 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67256679 | CTGAGAAGAGAGACG[C/G]CAACTGCACCCTTGC | 22992 |
rs566758798 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67191972 | TATCATGTGCATCTT[C/T]ACACTTAGTTTTGCT | 22992 |
rs566774394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67221360 | TATTAATGCTACTGC[C/T]CTTGAAACTTTTTGG | 22992 |
rs566837823 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67183579 | GCAAATTTCAGGGAC[A/C]GCTTGGACAATAAAG | 22992 |
rs566870026 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67199488 | GGATAAGAAAGAAAA[A/C]CAGCCTTATCACTGA | 22992 |
rs566870745 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67226794 | AAATTAAATGAGCAC[G/T]GGCCGCGAGCTGCTC | 22992 |
rs566875604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67182597 | GAGTGCAGTGGCACA[A/G]TCTCGGCTCACTGCA | 22992 |
rs566945455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67166805 | TGCTGGGCTGAGCGT[A/G]GTGGGTCATGTCTGT | 22992 |
rs566964127 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67190236 | CCAATGTGATGAAAC[C/T]CTGTCTCTACTAAAA | 22992 |
rs566974932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67159192 | GAGTTAATTTTTCTG[A/G]AAGGCATAAAGTTAG | 22992 |
rs566983621 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67175568 | GCTTGGAGACAGAAG[C/G]CTTCCTTGTATCCTT | 22992 |
rs567004707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67229613 | CGGTGGCTCACACCT[A/G]TAATCCCAGCACTTT | 22992 |
rs567039522 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67167014 | ACCTGGGAGACGGAG[G/T]TTGCAGTGAATTGAG | 22992 |
rs567062126 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67230899 | GTTAGAATTTCAACT[C/T]CAAAGCTTGATTTTA | 22992 |
rs567084293 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67166207 | TTTTTTTTTTTTTGA[G/T]ACAGTCTCACTCTAT | 22992 |
rs567093857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67236823 | ATTCCACCGCTCTGA[A/G]TAATGCCTGCCTGCT | 22992 |
rs567139433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67122456 | CTCAGCCTTGCAAGT[A/G]GCTGGGACTGTAGGC | 22992 |
rs567165884 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KDM2A | GRCh38.p7 | 11:67125368 | GTATTTTTTGTAGAG[A/G]TGGGGTTTTGCCGTG | 22992 |
rs567171900 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67174959 | AAGCCAGTAACTCCC[C/T]TTAGGCTGCTAAAAT | 22992 |
rs567187618 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67157640 | ATCCCAGCTACTCGG[C/G]AGGCTGAGGCACAAG | 22992 |
rs567191366 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67134701 | GTGGAGACAGGATTT[C/T]GCCACGTTGACTAGG | 22992 |
rs567192430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67228812 | CGTGATCATAGCTCA[C/T]TGTAACCTCAAACTC | 22992 |
rs567223580 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67144171 | GCTGGTCTCAAACTC[A/C]TGATGTCACGTGATC | 22992 |
rs567225696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67198448 | TTTCATTATGCCGGG[C/T]GCAATGGCTCATGCC | 22992 |
rs567229578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67236248 | TGATTCTCCTGCCTC[A/G]GCCTCCTGAGTAGCT | 22992 |
rs567280068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67137156 | CAACCAGCTAAGCCA[A/G]CCAACTAAACAAAAC | 22992 |
rs567289220 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67151049 | GAGGATATCATGGTG[A/G]ATAGTAGAAGCAGGG | 22992 |
rs567313033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67205360 | GTGGCCATATTCTTC[C/T]CTTGGGTATTATCTC | 22992 |
rs567373634 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67244861 | CATGGTGGTGGGCAC[C/G]TGTAGTCCCAGCTAC | 22992 |
rs567375470 | snp | C/T | 0.000373039 | 0.0136521 | intron-variant | KDM2A | GRCh38.p7 | 11:67254862 | CTGTCATTATGTCCA[C/T]TTTCCCGACAGGTTG | 22992 |
rs567389450 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67143643 | TTTATTTATTTATTT[A/T]TTTTTTTGAGATAGG | 22992 |
rs567432312 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67149978 | CTGCCCTCCTCAGCC[A/T]CCCAAAGTGCTGGGA | 22992 |
rs567461425 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67254105 | TACTTAACCCCTTCA[A/G]GGGGGCCTGGCCAGC | 22992 |
rs567489822 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67121528 | TGGCTTTTGGCCAAA[A/C]ATGTTTTATATTTTA | 22992 |
rs567500019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67243642 | AACATGGTGAAACAC[C/T]GTCTGTACCAAAAAT | 22992 |
rs567564483 | snp | C/G | 0.00716266 | 0.059414 | upstream-variant-2KB, missense | KDM2A, LOC107984341 | GRCh38.p7 | 11:67117913 | TCGGGCCGCGGGAGT[C/G]GGTCCGTGGGCAGGG | 22992 |
rs567574432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67227686 | GTGATTCTCATTCCT[C/T]AGCCTCCCGAGTAGC | 22992 |
rs567586549 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67253250 | TGTATTGCTCTGGTG[C/G]GAACTAAGCAATCAA | 22992 |
rs567602075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67220526 | TCTTTCTCAACTGGG[A/G]TTTCAAGAGAGAATT | 22992 |
rs567623321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67252468 | GGTAAAGTGGTCAAG[C/T]TATATACTATCAACA | 22992 |
rs567646817 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67165810 | TGTTCTTTCAGGTTT[A/G]TAGTAACCTTTCTTG | 22992 |
rs567673450 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67121000 | TGGTGTGGCCCTTCC[A/T]CAAGGAACTGAAACC | 22992 |
rs567682254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67172494 | TAAGTCTTGTACTTA[C/T]CTTGTTAAATTTATT | 22992 |
rs567686050 | in-del | -/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67198801 | TTGTTTTGTTTTTGA[-/C]GGAGTCTCACTCTGT | 22992 |
rs567701531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67127133 | GACAGGGTCTCACTC[C/T]GTTGCCCAGGCTAGA | 22992 |
rs567705557 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67179955 | AAAGAAAAGATCCAT[A/G]AGGCAAGGAAAATAG | 22992 |
rs567732278 | in-del | -/CAAA | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67162812 | TAAAATTCCTGGGCT[-/CAAA]CAGTCTTTCCACCTC | 22992 |
rs567762326 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KDM2A | GRCh38.p7 | 11:67180837 | TTTTTTTTTTTTATA[C/T]TTTTAGTAGAGACGG | 22992 |
rs567771640 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67156717 | GAGCGAGACTCCATC[-/T]CAAAAAAAAAAAAAA | 22992 |
rs567787561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67234626 | CTTGTCCTAGTGCTT[C/T]AGGCGGCAGACGCAG | 22992 |
rs567811066 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67188322 | CCCGTCTCTACTAAA[A/G]ATACAAAATATTAGC | 22992 |
rs567820997 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67230194 | AAAAAAAAAAAATAC[A/G]TCTAATAGAGCTAGG | 22992 |
rs567841060 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67230240 | CTGTAGTCCCAGCTA[G/T]TTGGGAGGCTAAGGC | 22992 |
rs567872318 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67218799 | TATTTTTACTAGAGA[C/T]GGGGTTTCACCATGT | 22992 |
rs567898310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67196379 | TCCTGGACTCAAGCG[A/G]TCTTCCTGCTTTAAC | 22992 |
rs567922414 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67142001 | GAAAATGACAGAATT[G/T]CATTCTTTTTTATGG | 22992 |
rs567936850 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67195763 | CAGTAAAGAAAATAC[G/T]TAACATAAGCCAACA | 22992 |
rs567979880 | in-del | -/CGGCTCA | 0.0130921 | 0.0798413 | intron-variant | KDM2A | GRCh38.p7 | 11:67182601 | GCAGTGGCACAATCT[-/CGGCTCA]CTGCAACCTCCGCCT | 22992 |
rs567987279 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67148346 | GGGTCGCTTGACCCC[C/T]GGAGGTTGAGGCTGC | 22992 |
rs567992896 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | KDM2A | GRCh38.p7 | 11:67200594 | ATGGCTCACTGCAGG[C/G]TCAGTGTCCCTGGGC | 22992 |
rs568028587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67155847 | TTTGGAACTCCCGAC[C/T]TCAGGTGATCCGCCT | 22992 |
rs568033059 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67186888 | GCCTGGGCAACATAG[C/T]AAAGACCCATTTCTT | 22992 |
rs568040768 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67128662 | GGGCCCCTAGAATGA[A/G]GATTAAATTTAAGCC | 22992 |
rs568127609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67163112 | CTGCCCTAGTCAGAC[C/T]GATATCCAGAATTTT | 22992 |
rs568129823 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67125907 | GAGATTGCACCATTG[C/T]ACTCCAGCATGGGTG | 22992 |
rs568132016 | in-del | -/TTTTGTTTTGTTTTG | 0.181621 | 0.240467 | intron-variant | KDM2A | GRCh38.p7 | 11:67198769 | CAGTAGTTTGTTTTG[-/TTTTGTTTTGTTTTG]TTTTGTTTTGTTTTT | 22992 |
rs568132242 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67187974 | CTGAGGCAGGACTGC[G/T]TGAAGCCAGGAATTC | 22992 |
rs568157060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67193987 | TGCTGAGATTATAGG[C/T]GTAATCTCACTGCAC | 22992 |
rs568161976 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67162336 | TAAATATATAATGCT[A/C]ACTTCTCCTGAAGCA | 22992 |
rs568167903 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67159088 | GTCTAAAAACCCATT[A/G]CCAAAGCCAAGGCCA | 22992 |
rs568187797 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, missense | KDM2A, LOC107984341 | GRCh38.p7 | 11:67118004 | AACAGGAGACATCTT[C/T]CCGGCCGGGCCTCCC | 22992 |
rs568192970 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67193097 | CAGGTTCAAGTGATT[C/G]TCCTGCCTCAGCCTC | 22992 |
rs568228490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67125563 | GATCACCTGAGGTCA[A/G]GAGTTTGAGACCAGC | 22992 |
rs568234052 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KDM2A | GRCh38.p7 | 11:67170412 | TTTCTTTCTTTCTTT[C/T]TTTTTTTTTTTTTTT | 22992 |
rs568238053 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67191605 | TACATGATCATCTCA[A/G]TTGACACAGAGAAGG | 22992 |
rs568248367 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67126173 | ATCGCTTGAACCCGC[A/G]AGACAGAGGTTGTGC | 22992 |
rs568254177 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67122535 | GTTTTACCATGTTGG[C/T]CAGGATGATCTCGAT | 22992 |
rs568272931 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67225663 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 22992 |
rs568276690 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67178813 | TGACATTTGGGTGGT[G/T]TCTATCTTTTGGCTG | 22992 |
rs568280347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67200964 | TTTGGGAGGTCGAGG[C/T]GGGTGGATCACGAGG | 22992 |
rs568286358 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67169684 | CTCAGCCCATCACTT[C/G]GTTTCTTTTTTCTTT | 22992 |
rs568292835 | snp | A/C | | | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67120025 | TACTTCTCACTTGGA[A/C]AAGAACTCAAGAGCA | 22992 |
rs568318023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67186357 | CCAGTGTATTCAAAG[C/T]GCTAAAAGGAAAACA | 22992 |
rs568320125 | in-del | -/TGTGTGTGTG | 0.00242718 | 0.034752 | downstream-variant-500B | KDM2A | GRCh38.p7 | 11:67258453 | CATGTCCAGCTAATT[-/TGTGTGTGTG]TGTGTGTGTGTGTAT | 22992 |
rs568346622 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | KDM2A | GRCh38.p7 | 11:67240674 | CCGAATGCCTGGAGC[C/G]GAGATAGGCGTCAGC | 22992 |
rs568381255 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67152831 | TTTTGTAGAATCAGA[-/T]TTTTTTTTTTGCTAG | 22992 |
rs568389666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67241396 | TCTGGAGACTTGGCA[A/G]AAGGGGATCTTAGTA | 22992 |
rs568417796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67168425 | CTATAATTTATTTAC[A/G]TATTTGTTGCCCCCT | 22992 |
rs568499549 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67146192 | TAGAGACAGGGTTTC[A/T]CCATGTTGGCCAGGA | 22992 |
rs568536691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67154269 | TTTACGTCTTTTAAT[A/G]TATAATTGTTTTAAA | 22992 |
rs568537869 | snp | C/T | 5.48431e-05 | 0.00523627 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67250109 | AATGGAAGAGAGTGA[C/T]GAAGAAGCTGTGCAA | 22992 |
rs568541881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67139640 | TGCCTCAGCCTCTCA[A/G]AGTACTAGTATTACA | 22992 |
rs568559777 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67257806 | AAGGGGATAAGTCTT[A/G]TGCTATCTCAGTTGA | 22992 |
rs568573060 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67249754 | TCAGACTCAGGATCT[C/T]AGTTCAAATGGTATA | 22992 |
rs568627952 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67121874 | ATTGAAGACAAGTAG[A/G/T]TAGAATACTGGATGC | 22992 |
rs568638811 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67138810 | GGACTCAACAGCCTG[G/T]GTTTCAACTAGTTCT | 22992 |
rs568657150 | in-del | -/AAAC | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67136459 | GAGATTCATTCACTT[-/AAAC]AAATGTTTGTTGAGT | 22992 |
rs568662732 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67257807 | AGGGGATAAGTCTTA[C/T]GCTATCTCAGTTGAC | 22992 |
rs568698728 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67138228 | TCTGTAAGTCAAGGA[A/G]TATGCTTTATTCAGG | 22992 |
rs568700591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67145542 | AGGGGGAATATGGTA[A/G]CACCCCATTTTTTTT | 22992 |
rs568749358 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67194765 | GGCCTTTATCTCAGC[A/C]AGCTACCTGGCTTCT | 22992 |
rs568763679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67144984 | ATGTGATTCTCCTGC[C/T]TCAGCCTCTCAAGTT | 22992 |
rs568773216 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67124732 | TTTTCTTTAAGTTGT[A/G/T]AGGTGATTGGTACTT | 22992 |
rs568787750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67176734 | GCAGTTATAGCATGC[C/T]AGTAAATATTTGTGT | 22992 |
rs568807235 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67223874 | TATTTAATTTTGAGG[G/T]ACCAAATACCTATTG | 22992 |
rs568818841 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255605 | GTTGAGATCTCCCAA[A/T]CCTCACGTCCTTAAC | 22992 |
rs568822639 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67130776 | ATTTATTATATGCCA[C/G]ATAGTAGGCTAGGTT | 22992 |
rs568826233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67177261 | ACAGAGCAAGACTCC[A/G]TCTCAAAAAAATATT | 22992 |
rs568829965 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67142787 | TAAATCCTTATTCCT[A/C]GAAGTACAGTAATTA | 22992 |
rs568862860 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67119908 | CAACTGTTTGCTCCC[C/T]TTTCCTGGTCGCTCT | 22992 |
rs568875752 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67184433 | AGGAGTTCGAGACCA[C/G]CCTGACCAACATGGT | 22992 |
rs568890688 | in-del | -/AA | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67182523 | TGGTCAGTAAAATTG[-/AA]TAAGTCTTTTTTTTT | 22992 |
rs568904341 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67238245 | ACTTACTGGGAGTGA[A/G]TTTCCTAGTGCCCGA | 22992 |
rs568922387 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255876 | CTCTCTTTTGCCTCC[C/T]ACTGACTGCCCTTTT | 22992 |
rs568934051 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67230093 | AGGCAGAAGAATGGC[G/T]TGAACCCAGAAGGTG | 22992 |
rs568940643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67248176 | GTTTTTCTCCCTTTA[C/T]GGACCAATGTTGTTG | 22992 |
rs568969320 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67123164 | TTTTTTTCTTAGTGA[C/T]GGGGTCTTGCTATGT | 22992 |
rs568993459 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67159478 | CTTAAACATTTTGGC[A/G]AGAATGTTTCCCAGA | 22992 |
rs569006636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67221964 | AAAAAGATGTCTATT[C/T]TAAAATAGGTAAATA | 22992 |
rs569028744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67191918 | TGGCAGATGATATGA[C/T]TTTTTTATTTGTTAT | 22992 |
rs569031801 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67162394 | AAGTAGATATGATTT[C/T]TATTTTATTTTATTT | 22992 |
rs569051291 | in-del | -/TTTC | 0.00953873 | 0.0683987 | intron-variant | KDM2A | GRCh38.p7 | 11:67154423 | TACCTATTCTGGGTG[-/TTTC]TTTCTTTCTTTCTTT | 22992 |
rs569124207 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67205771 | ATAGATGTGCACCAC[C/T]GTGCCCGGCCAGACA | 22992 |
rs569129017 | in-del | -/TT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67182549 | TTTTTTTTTTTTTTT[-/TT]GAGACGCAGTCTCCC | 22992 |
rs569151794 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67199367 | TTTAGTGATTAAGGC[A/C]TGTCAAAAGCCAAGA | 22992 |
rs569179656 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67122710 | AGACAGAGTCTGGCT[C/T]TGTTGCCCAGGCTGG | 22992 |
rs569217294 | snp | C/T | | | intron-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67120519 | TATTTAATTTTTGGA[C/T]AAGATGTATTTTCCT | 22992 |
rs569237820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67205502 | TATAAATTTTTTTTT[C/T]CTACAGCCTCGACCT | 22992 |
rs569271641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67158413 | GGTTTTTGTGTGGAC[A/G]TGAGTTTTCAATTCA | 22992 |
rs569295822 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67122417 | CCGCAGCCTCCACCT[A/C]CTGGGTTCAAGTGAT | 22992 |
rs569309032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67166770 | GTTCAGGTTGGAAAC[C/T]GAGCAGGTCAAAACT | 22992 |
rs569331151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67213798 | ATTCTCACATTATTT[C/T]AGATTTTAAAAGTGT | 22992 |
rs569433422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67174783 | GTCATCTAAGTAGAA[C/T]AAAGTAATTTGTTGT | 22992 |
rs569433671 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67190058 | GATAAACAAAATTGA[C/T]AAAGCTTTATTTAGC | 22992 |
rs569481016 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67203616 | AAAAATTAACTGGGT[A/C]TGGTGGCATGCACTG | 22992 |
rs569497447 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67128539 | GTTGCGGCCTCCCTC[C/T]TAATAATGTAGGAAA | 22992 |
rs569538559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67136940 | CAAAGGTAAACATAG[A/G]CTGCAGTAACAGTAT | 22992 |
rs569551469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67164199 | GAAGCTCAAAGTGGC[A/G]GTGCCTAGACCCAGA | 22992 |
rs569598058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67136024 | TGTGTTTGTTTAATA[C/T]CTGATTTTTTCACCA | 22992 |
rs569622090 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67149869 | GGGATTACAGGCATG[A/C]GCCACCAGTCCCAGC | 22992 |
rs569627170 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67186908 | ACCCATTTCTTCCAC[C/T]CCATGAATGAATGAA | 22992 |
rs569658381 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67143527 | GAAATTGCCACCACT[G/T]CAAAAGCTTCTTTAC | 22992 |
rs569661320 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67157618 | GACACAGTGGCACGC[A/G]CCTGAAATCCCAGCT | 22992 |
rs569719145 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67142862 | AGTAAATAGTGGTGT[C/G]ATTAACACCCATATA | 22992 |
rs569721326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67212549 | ATGATATTGGACTTC[C/T]TACCAGTTTGGCCCT | 22992 |
rs569737390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67254092 | GTGTGGGCAGTTCTA[C/T]TTAACCCCTTCAAGG | 22992 |
rs569742993 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67149101 | CCCTGAAGCTCTTTA[A/G]TAATGGCAAAAGTTA | 22992 |
rs569779068 | in-del | -/TTAT | 0.0316359 | 0.121726 | intron-variant | KDM2A | GRCh38.p7 | 11:67223392 | TTTTTTCTTTCTTAT[-/TTAT]TTATTTATTTATTTA | 22992 |
rs569829364 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67216597 | AGAAAAGTAGGAACT[A/G]GAATGAGAATAGATA | 22992 |
rs569830852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67157312 | ACAGAGCAAGACTCC[C/T]GTCTCAAAAAAAAAA | 22992 |
rs569844196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67141969 | TATTTAATATTCTCC[A/G]ATTCCATCCATGTTC | 22992 |
rs569886408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67218351 | GGATTCTGACTATGC[A/G]TTTACCTGCTAGATA | 22992 |
rs569926159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67219235 | TAGTTCTCTGAGAGA[A/G]ACTTACTGTAATGTG | 22992 |
rs569948808 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67213022 | ATGCTTGGTTAAAAT[C/T]GTTGGCTCCCTGAGC | 22992 |
rs569986695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67147422 | TGGCGGGTGCCTGTA[A/G]TCCCAGCTACTCAGG | 22992 |
rs570058844 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67145135 | GCTTGGCCTCCCAAA[A/G]TGCTAAGATTACAGG | 22992 |
rs570086340 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67234529 | AAGAACAAGTCATAG[A/C]ATATAGAGTTGGAAG | 22992 |
rs570101623 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67134092 | AATGAAATACTAAGG[G/T]AGACTTTGGGATTTA | 22992 |
rs570105549 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67147085 | AAACAGAGCTAAGAT[C/T]TATGAAAGTGTCTGC | 22992 |
rs570137524 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67241699 | TGCTGTTGGTGTTGC[A/T]TTAGGGCTCATAAGG | 22992 |
rs570217927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67252255 | CATTTCAGGCAGCTG[C/T]GAGTGATTGACAAGG | 22992 |
rs570233352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67195660 | ATTAGTTGTTCATGC[C/T]CTATGCAGTCTGTAT | 22992 |
rs570237640 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67196061 | TTTATTGCGTACCCA[C/T]CCCATCCCAGTTAAG | 22992 |
rs570246014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67224742 | AAGTGCTGGGATTGC[A/G]GGCTTGAGCTATCTT | 22992 |
rs570270556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67194798 | ACTCCTACTTTGATT[C/T]ACCTGCTGTTGCAGC | 22992 |
rs570328490 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67123146 | GGGTAATTTTCAGAC[-/T]TTTTTTTTTCTTAGT | 22992 |
rs570333806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67232100 | CATGTGTGTTTGTTA[C/T]TGCTGCTCAGTGTTT | 22992 |
rs570337213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67155750 | GCCTCCTAAGTAGCT[A/G]TGATTACAGGCATGT | 22992 |
rs570358228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67202212 | AAGAGTTGCTTCTTA[C/T]GGATGAGCAAATAAA | 22992 |
rs570358737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67208976 | TCTCACATTGTTGCC[C/T]GGGATATAGAGTGCG | 22992 |
rs570371659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67231066 | GGCTCAAGCAGTCTT[C/T]CCACCTCACCCTCCC | 22992 |
rs570449179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67216795 | TGTGGTGGTACATGC[C/T]TATAATCCCAGCTAC | 22992 |
rs570468996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67208315 | TGGGCTCAAGCAGTT[C/T]TCCCACCTTGGCCTC | 22992 |
rs570517419 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67171848 | AAAATCAATTCACTG[A/T]AAGTGTAAGAGTTTA | 22992 |
rs570526222 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67156468 | TCTCGGCTGTAATCC[C/G]AGCACTTTGGGAGGC | 22992 |
rs570526562 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67191188 | GCTGGGATTATGCCC[A/G]GCTAATTTTTTGTAT | 22992 |
rs570563301 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67187533 | AAACAGACATTTATT[A/T]ATTTATTTAATTGAT | 22992 |
rs570585873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67169602 | GCTGCTCTTGAACTC[C/T]TGACCTTAGGTGATC | 22992 |
rs570607108 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67200365 | GGACTACAGGCGTCC[A/G/T]CCACCACGTCCGGCT | 22992 |
rs570616093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67223324 | ATTAATACAGTCTTA[C/T]AAGTTACGAGTAAAA | 22992 |
rs570617731 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67178009 | TGAAATGTCATTATA[C/G]TGTGCATGACTGTAT | 22992 |
rs570630743 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67132735 | AAGGCAGTGGTTTTC[A/T]AAGTGTAGGTCTCTC | 22992 |
rs570671180 | snp | C/T | | | downstream-variant-500B | KDM2A | GRCh38.p7 | 11:67258109 | CTGCTTCGGTGTGTG[C/T]GTGTGAGCAAGTCAG | 22992 |
rs570671371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67186298 | CTCAGTAAAATTATG[A/G]ACGAATTTCTCATCA | 22992 |
rs570684977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67139596 | GTTGCCCAGGCTGGT[C/T]TTGAACTCCTAGGCT | 22992 |
rs570685781 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67240632 | TCCTGTGATCTGTAG[G/T]GTGTGGGCTTGTGTT | 22992 |
rs570700223 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67195784 | TAAGCCAACAATTGT[C/G]AGCTTGTCCTAATTT | 22992 |
rs570704208 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67177449 | AAGCTTTTGTCTACT[A/G]AAGTTTTTTTTTTAA | 22992 |
rs570708006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67193792 | CTTGAACCCAGGAGC[A/G]GGAGGTTGCGGTAAG | 22992 |
rs570729069 | snp | C/T | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67193012 | TTGGCTAGGGGGTAT[C/T]AGAGTCTCACTTTGT | 22992 |
rs570773166 | snp | A/G | 1.95071e-05 | 0.003123 | intron-variant | KDM2A | GRCh38.p7 | 11:67250040 | CGGTTCAGAGGGTTT[A/G]GAAGAAAGGAAGCAC | 22992 |
rs570820720 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67251698 | GGACTCTGATGCATG[C/T]TCGAGTTTAGAGCAG | 22992 |
rs570829803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67176666 | TATATGGTATATCCT[A/G]TAGCTTCTAGGCTAC | 22992 |
rs570832000 | in-del | -/AATG | | | intron-variant | KDM2A | GRCh38.p7 | 11:67215081 | CACTATTGCATAATT[-/AATG]ATTCCATTTTGACTA | 22992 |
rs570832260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67192239 | CCCTTGGTTTTTAAT[A/G]CAGTCTGTAGACATG | 22992 |
rs570873588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67184226 | TGGCCGGGTGCAGTG[A/G]CTCATGTCTGTAATC | 22992 |
rs570899139 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67119919 | TCCCTTTTCCTGGTC[A/G]CTCTGACCCTCTCTG | 22992 |
rs570912299 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67145689 | ATTATACCATATTCT[C/G]CCTTTCTCTTTTCTC | 22992 |
rs570931366 | in-del | -/TCC | 0.00279162 | 0.0372561 | intron-variant | KDM2A | GRCh38.p7 | 11:67251116 | TGCGGGCTGAAAATT[-/TCC]TCCTCAAGTCAGCTG | 22992 |
rs570932642 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67257711 | TTTCGGAGAAATATT[A/G]TAAATATATATTTTT | 22992 |
rs570933970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67160792 | AAACAACAAAAAAAA[A/G]ATGAGATAGACCTTC | 22992 |
rs570934096 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67256940 | TTTGAGGAAATGCCA[A/G]TGACTTATTCCAGAG | 22992 |
rs570952868 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | KDM2A | GRCh38.p7 | 11:67225426 | GAATCACTGGAGTTC[A/G]GGAGTTCGAGACCAA | 22992 |
rs570953870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67160021 | GTAAACTTTATGTGT[A/G]TATTACCACACACAT | 22992 |
rs570959631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67183650 | CAGCTGCTCCATTCT[C/T]CCCTGCCAACCAAGC | 22992 |
rs570965453 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67153205 | GGTCAGGCTGGTCTC[A/G]AATTCCTGACATTGG | 22992 |
rs570974709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67215629 | ACCATAGCACACAAC[C/T]ACACAGTTAAAGGAA | 22992 |
rs570988689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67167597 | CTATCTTTTTTTTTT[C/T]CCTTAAAGGTCCTAC | 22992 |
rs571011166 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67223147 | CAGTGAGCCAAGATC[A/G]TGCCATTGCACTCCA | 22992 |
rs571041838 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67144883 | TTATTTTTATTTATA[G/T]TTTTGAGACAGAGTC | 22992 |
rs571079980 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67214707 | AAACTCCTGGGTTCA[A/C]GTGATCTTCCCACCT | 22992 |
rs571112098 | in-del | -/TA | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67257589 | GAAAGGAAGAAAATT[-/TA]TATATATATATAATA | 22992 |
rs571142260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67123988 | GGACTTTTGGGTTTT[A/G]TTGTTGTTGTTTGTT | 22992 |
rs571164350 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67130108 | GCTGGGATTACAGGC[A/G]TCCGCCACCCCACCT | 22992 |
rs571165053 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67222161 | CAATAGTGGAGGGAA[A/G]GTCAGCAGATAAACA | 22992 |
rs571175306 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67151525 | GGCTAATTTTTTGTA[G/T]TTTTAGTAGAGACCG | 22992 |
rs571183226 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67248600 | ACTTGGGATCTGCAA[A/G]TTCCTAAGGTCCTTT | 22992 |
rs571208084 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67123143 | CCAGGGTAATTTTCA[C/G]ACTTTTTTTTTTCTT | 22992 |
rs571214879 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67150187 | TACAGCTGTTTAGCC[C/T]GGAAATATGCATTTG | 22992 |
rs571241789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67229645 | GGAGGCTGAGGCGGG[C/T]GGATCATGAGGTCAG | 22992 |
rs571257435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67247247 | AGCACGTGCCACTGC[A/G]CCCAGCTAATTTTTG | 22992 |
rs571287363 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67129374 | CCAGTGGAATGCTTG[A/C]CGTCAGGAGTTGAAG | 22992 |
rs571326316 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67199206 | TGCTATTCCCTTGTT[C/G]TCTTTCTCTCCTCAG | 22992 |
rs571327142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67122289 | TCGAATACATTTTCT[A/G]GTGATCCTTACTCTT | 22992 |
rs571329881 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67236887 | CTATGCAGACATGCC[A/G]TGGTCCTAGCCCTCA | 22992 |
rs571334917 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67244727 | GTGGTGGCTCACACC[G/T]GTAATCCCAGCACTA | 22992 |
rs571390394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67121590 | TGTAGCCTTTAGCTT[C/T]TATAGAAACCATTGT | 22992 |
rs571390748 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67190265 | AAATACATAAATTAG[C/G]TGGATGTGGTGGTAC | 22992 |
rs571405190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67246197 | ACACTTGTGATGGGA[A/G]TGCCAGCATCCCTAC | 22992 |
rs571413880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67236318 | GTATTTTCAGTAGAG[A/G]TGGAGTTTTACCATG | 22992 |
rs571450875 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67128277 | GCCTCTCCAGCCTCC[C/T]CAGCTCCTGGGATTA | 22992 |
rs571452924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67121034 | ATCTCGTTTCGTCTA[A/G]GCCTCCGACAGTTGT | 22992 |
rs571458441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67158176 | CCCTTTCTAAAATGT[C/T]GTATAGTTGGAATCA | 22992 |
rs571516224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67127785 | CAATCTGGGCTCACC[A/G]CAACCTCCCTCTCCT | 22992 |
rs571593466 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | KDM2A | GRCh38.p7 | 11:67213628 | GTTAGGTGCGGTGGC[C/G]GGTGCCTGTAATCCC | 22992 |
rs571609971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67243763 | GAGGTTGCAGTGAGC[C/T]GAGATCGCACCATTG | 22992 |
rs571668751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67220545 | CAAGAGAGAATTAAG[C/T]CCAAAATAAAATAAT | 22992 |
rs571684454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67212876 | AGTACTTTATTCATT[A/G]TTCTGTTAAAGGCAT | 22992 |
rs571698025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67242854 | GATTTATTTGTTTTC[C/T]AGTGAGTCTCTATAT | 22992 |
rs571706962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67237242 | TGATCTAAAAATTTA[C/T]GTTAGGCCCCATCCC | 22992 |
rs571754746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67135717 | CTTTTTGTCATTTTA[A/G]TCTTTTGATCATCAC | 22992 |
rs571756182 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67227869 | TGTTTCTCAAGACCA[A/G]CGTTTTCTAAGTTGA | 22992 |
rs571792133 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67202604 | GGTGAAACCCCGTCT[C/G]TACTAAAAATACAAA | 22992 |
rs571825248 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67173322 | AGACGGGGTTTCTCC[A/G]TGTTGATCAGGCTGG | 22992 |
rs571830758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67181583 | GGTAAATGAGAAAAT[A/G]TAGATGAACCAAAAA | 22992 |
rs571868861 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67120779 | CCTAATTTTTTGTCC[C/T]CTTTTTACATAGTCA | 22992 |
rs571878630 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67134926 | GAATTTTCACAAAAC[G/T]AACTTCATGGTCATG | 22992 |
rs571894747 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67139704 | AAGGTTGCTGCTGCT[A/G]TTTTTTTTTTTAATT | 22992 |
rs571896731 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67188362 | TGGCAGGCGCCTGTA[G/T]TCCCAGCGACTCGGG | 22992 |
rs571963780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67208562 | ATCACCTGAGGTCAG[A/G]AGTTTGAGACCAGCT | 22992 |
rs571999270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67133792 | CTATAACTTCCGCCT[C/T]CCAGGTTCAAGCGAT | 22992 |
rs572006579 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | KDM2A | GRCh38.p7 | 11:67243298 | CTCTTAACAGAACTA[-/T]TCAAACTGGGAGGCC | 22992 |
rs572040723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67179388 | AAGCGATTCTCCTGC[A/G]TCAGCCTCCTGAGTA | 22992 |
rs572045132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67187952 | AAAATCCCAGCACTT[C/T]GGGAGGCTGAGGCAG | 22992 |
rs572063174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67140702 | AGGTTGCAGTGAGCC[A/G]AGATTGTGCCATTGC | 22992 |
rs572078182 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67187509 | GGGTAGCTATACTTA[C/T]ATCAGATAAAACAGA | 22992 |
rs572089768 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67216501 | ATATGAGAATGGAAA[A/T]CTAGAATTAATACCC | 22992 |
rs572099270 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67209320 | AATTTAGCCTTCTTA[C/T]TAGCCTAATGTGATT | 22992 |
rs572101939 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67195180 | TCTAAATAGTCTCAG[A/T]TTATCCATGACTTGA | 22992 |
rs572117721 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67251866 | TGTATCTAAATTCTC[C/T]TTAATATTTCTCTGT | 22992 |
rs572123207 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67213425 | AGTGTAAAATGTTGC[A/G]TATTGCTTTCACTTC | 22992 |
rs572144260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67251041 | CCATGTCTCATTGTT[A/G]TGGGGAGGGAGACTG | 22992 |
rs572155147 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67178432 | ATAAAATAAAGTGTA[C/G]AATCCAGTGGTTTTT | 22992 |
rs572177965 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67147673 | TGAGTAGTTCCCTTT[A/C]ATTAGAGATTCTTTT | 22992 |
rs572187162 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67245654 | ATCCGATTTAATCTT[C/T]AGGCTTTACCTAATT | 22992 |
rs572193716 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67177555 | CACAGAGCGGCATCA[G/T]TATCACTGTCTTCCG | 22992 |
rs572280165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185739 | AGATAATTAGGCTAC[A/G]GGGACTCCACTCTCA | 22992 |
rs572289725 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67240665 | AATGTTCTCCCGAAT[A/G]CCTGGAGCCGAGATA | 22992 |
rs572301257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67155405 | CGTCATACTCCTAGG[C/T]TCAAGCGATTATCCT | 22992 |
rs572305901 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67161231 | GAAACCAAAAACAAA[A/C]GAAAAACAAGACTTT | 22992 |
rs572317302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67184757 | CATATGCACATGGAC[A/G]GTCAGGCTCAGAGAA | 22992 |
rs572326527 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67161748 | TCAAAACTATTTTCA[G/T]AACAGTACTATTATT | 22992 |
rs572363937 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67169821 | AGAGTACAGTGGCGA[C/G]ATCTCGGCTCACTGC | 22992 |
rs572394361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67169250 | TGAGCCACTGCACCC[A/G]GCCTAATCCATGTAG | 22992 |
rs572452683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67231400 | CTACCTGTTAACTGT[A/G]ATTTTGAACAGTGGA | 22992 |
rs572537590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67152557 | AGGCTGCAGTGATCT[A/G]TGATCATGCCACTGC | 22992 |
rs572576023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67136961 | GTAACAGTATATGAT[A/G]GAGTGAGCTAATCTA | 22992 |
rs572595717 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67139716 | GCTATTTTTTTTTTT[A/T]ATTTATTTTTTGAGA | 22992 |
rs572608306 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67139330 | GCTCATTGCAACCTC[C/T]GCCTCCCAGGTTCAA | 22992 |
rs572610653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67193235 | CCTCAGGTGATCCAC[C/T]CGCCTCAGCCTCCCA | 22992 |
rs572666629 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67146340 | CATAAGAAATAATAC[A/T]CCGATTGTCTTTTTA | 22992 |
rs572667186 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-5-prime, intron-variant | KDM2A | GRCh38.p7 | 11:67240047 | CTCCTGCCATCTTCC[A/G]TTGCAAAGCATTTCT | 22992 |
rs572667829 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67200278 | TGGAGTGCAGTGGCA[C/T]GATCTCAGCTCACTG | 22992 |
rs572668724 | snp | C/G | | | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67238826 | GGCTCTAAAAAAGAC[C/G]CAAACTGTTTCTGCT | 22992 |
rs572669350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67169668 | GGCATGAGCCACTGC[A/G]CTCAGCCCATCACTT | 22992 |
rs572673340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67131417 | GTTTTCTTTTCTTTT[C/T]TTTTTTTTTTTGAGA | 22992 |
rs572685586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67200503 | ATTATAGGCGTGAGC[A/G]ACCGTGCCCAGCCTG | 22992 |
rs572696653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67201009 | CCATCTGGCTAACAC[A/G]GTGAAACCCAGTCTC | 22992 |
rs572706230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67249876 | GTGGCTCACACCTAT[A/G]ATTCCAGCACTTTGG | 22992 |
rs572733315 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67232443 | ATTGGGAAAAGCATC[A/T]TTTTAAAATAATTCA | 22992 |
rs572751970 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67196836 | ATAACACTGAACTGT[A/G]CTCCTAAAAATGGTT | 22992 |
rs572793019 | snp | A/C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67164464 | TTAAGTGTTGATCTT[A/C/G]CTATTGGCCTTTTTT | 22992 |
rs572801830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67237033 | AGAGTGGCAGAGTCT[A/G]TCCTGAGGGAAAGAG | 22992 |
rs572832695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67129659 | GAATGGTGTGAACCC[A/G]GGAGGCGGAGCTTGC | 22992 |
rs572889908 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67160145 | ATTAGGACTAATTGG[A/G]AGAAAAACTCTTCCT | 22992 |
rs572891355 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206877 | CTGATATAGATTTTC[A/G]TGTCCATCCTGGTGT | 22992 |
rs572891531 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67247412 | TAGGATATTTTAACA[A/G]CATTACAATCTTTTT | 22992 |
rs572926667 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67192888 | TTCCTCTCCAAAGTG[A/G]TTGTACCAGTTTACA | 22992 |
rs572926669 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67246516 | AGGATAATAATATCA[A/G]ATAACATTTAATGAG | 22992 |
rs572927461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67215774 | GATAAAGGGAGTATA[C/T]AAGAGGAGAGTATGG | 22992 |
rs572943602 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | KDM2A | GRCh38.p7 | 11:67125279 | TCGACATCCTGGTCT[C/T]GAGTGATCTTCCCAC | 22992 |
rs572982834 | in-del | -/G | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67125456 | AACAAGTCATTTTTT[-/G]GGGGGAAAAAAAAAT | 22992 |
rs573000148 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | KDM2A | GRCh38.p7 | 11:67176108 | TGTGATTTGTGGCAG[C/G]CAAGTTACTAGGTAA | 22992 |
rs573016877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67215066 | GAGTTCATAGTTATA[C/T]ACTATTGCATAATTA | 22992 |
rs573022588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67229819 | AGGTTGCAGTGAGCC[A/G]AGATCACGCCACTGC | 22992 |
rs573093835 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67126673 | AGATCACACCACTGC[A/G]CTCCAGCCTGGGCGA | 22992 |
rs573123963 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67138320 | AATGTAGAGAACACA[A/G]TAAGTGAATTTCAAC | 22992 |
rs573147169 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67124196 | TTTAGTAAAGATGGA[A/G]TTTCACCATGTTGGC | 22992 |
rs573151442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67137675 | ACTGAGCAAAGGAGC[A/G]TAAGTTCAGTTTTGA | 22992 |
rs573215118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67144435 | TTTTGTATTTTTAGT[A/G]GAGTTGGGGTTTCTC | 22992 |
rs573241326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67220747 | AGTGTCTATTGTAAC[C/T]GTTTAACCCTACCTT | 22992 |
rs573247094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67183232 | AATGCTCCCCTACTC[A/G]TCACAAGACAGAACA | 22992 |
rs573271901 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255212 | CAGGTGGGGCAGAGA[A/G]GGTGGTGGACACCAG | 22992 |
rs573277153 | snp | A/C | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67184534 | TCAGGAGGCTGAGGC[A/C]GGAGAATTGCTTGAA | 22992 |
rs573278697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67219868 | ATAAAAATTTTAACA[C/T]GATTTACATACTCCG | 22992 |
rs573292366 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67156705 | GCCTGGGCAACAGAG[C/T]GAGACTCCATCTCAA | 22992 |
rs573307682 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67143903 | TCCCAAAGTGCTGGG[A/T]TTACAGGCATGAGCC | 22992 |
rs573322021 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67197946 | AAACAGTTGATTAAC[A/G]TATTTTATGTTATAC | 22992 |
rs573340182 | snp | C/G | 2.43377e-05 | 0.0034883 | intron-variant | KDM2A | GRCh38.p7 | 11:67254520 | GGTCTGTTGATTGAC[C/G]CACATCAGCTCATTT | 22992 |
rs573341763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67181944 | AAGATTTAAGACTTA[A/G]GACTGAATTAAATCT | 22992 |
rs573342482 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67224769 | TCTTGTCCGGCCAAA[A/G]TTAATCCCTTTCTCA | 22992 |
rs573350376 | snp | A/T | | | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67238740 | AAGAGCTAGATGCTT[A/T]AATCAGAGCATCTGC | 22992 |
rs573377431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67150437 | TTGATTCTCAAGTGT[A/G]TTTAAATTATTTTTG | 22992 |
rs573378822 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67151647 | ATAAGCCACTGGACC[C/T]GGCCTCAAATCCTGA | 22992 |
rs573466066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67188537 | GCCTCACACGTCTGT[A/G]ATCCCAACTTTGGGA | 22992 |
rs573473884 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67165698 | CTATCTCCCTTAATT[A/C]ACTTAAAGACTTAGG | 22992 |
rs573506198 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67121849 | TAGCTTTGAAGGGTT[C/G]TTGGGATTGATTGAA | 22992 |
rs573511317 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67188104 | TCCTAGCCACTTGGA[A/G]GGCTTGAGCCCAGGA | 22992 |
rs573511692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67173957 | CTTCAGAAAGTGATC[C/T]TCCTACCCCAGCCTC | 22992 |
rs573531665 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67228229 | TGAGGCCCGAAATAC[C/T]CAGTAGGCTGTCACT | 22992 |
rs573597276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67196204 | GCAAAATCATCCATG[A/G]TGCACGAGCAGGGGC | 22992 |
rs573622813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67172965 | TTATGGAATATTTAT[A/G]GACATAATGTGATGC | 22992 |
rs573625222 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67200975 | GAGGCGGGTGGATCA[C/T]GAGGTCAGGAGATTG | 22992 |
rs573643689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67227410 | ATTCAGGGGCAAATA[C/T]AGTAAAGCAAGAGTA | 22992 |
rs573680353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67234946 | GGTCAGGAGATCAAG[A/G]CCATCCTTGCTAACA | 22992 |
rs573689975 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67156846 | GTGAGCCGAGATCGC[A/G]CCACTGCACTTCATC | 22992 |
rs573691071 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67128558 | TAATGTAGGAAAAAC[G/T]TGACCATTTTTGGGT | 22992 |
rs573726919 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67163314 | CGGTGGCAGGATACA[C/G]TTGTTGAATTTCATA | 22992 |
rs573752532 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67127962 | CGATCTGCCTGCCTC[A/G]GCTTCCCAAAGTGCT | 22992 |
rs573814343 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67162653 | TCAAGTGATCCGCCC[G/T]CCTCGGCCTCCCAAA | 22992 |
rs573816524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67135139 | AATGGCGCGATCTCG[C/T]CTCACCACAACCTCC | 22992 |
rs573873876 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67244192 | AGTCATTTCTGGTTG[A/T]TGAGTATTTTGTGTC | 22992 |
rs573875937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67134654 | GGATTACAGGTATGC[A/G]TCGCCACGCCCAGCT | 22992 |
rs573907113 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67243224 | AACTGACAGAAAATC[A/T]TTATTCAGTTCTGTT | 22992 |
rs573915778 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67203155 | CCAAGATTATGACTC[A/T]CTGAAGGCTCAGATG | 22992 |
rs573943246 | in-del | -/TGAGACCAGCCTGGACAACAGAGCAAGAGATG | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67152399 | GGTTGGAGGGTCGTT[lengthTooLong]TGAGACCAGCCTGGA | 22992 |
rs573984768 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67163132 | TCCAGAATTTTGCTC[G/T]TGCATAACTTCATTG | 22992 |
rs574030024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67133096 | ATTGTGCTTTTATTC[A/G]TATTTATTTATTTAT | 22992 |
rs574035374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67120196 | AGATTCGCCCTTTTT[C/T]CTCTCCGGCCCTGGC | 22992 |
rs574068317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67171731 | TATTTGATACAAACT[A/G]GGTCTCAAACTCCTG | 22992 |
rs574076974 | snp | C/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206939 | ATGAAAAGGGGACTT[C/T]GTTCTTCATGAACTA | 22992 |
rs574090400 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67226448 | AGATTTCCAGCCAGG[C/T]GCAGTGGCTCACGCC | 22992 |
rs574092333 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67140497 | TGGTTCACTCCTGTA[A/G]TCCCAGCACTTTGGG | 22992 |
rs574101313 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67160767 | AAAGAGTGAAACTCC[A/G]TCTCAAAAAAAACAA | 22992 |
rs574127117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67250876 | TGAGAACAGCATGCA[C/T]CTTGGCATCTGAAAG | 22992 |
rs574136899 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67193659 | TGAGGTCGGGAGTTC[A/G]AGACCAGCCTGACCA | 22992 |
rs574213446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67179329 | CCCAGGCTGGAATGC[A/G]ATGGCACGATCTTGG | 22992 |
rs574239260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67233393 | GTGCGATGTCTCATG[C/T]CTGTAATCCCAGCAC | 22992 |
rs574247181 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | KDM2A | GRCh38.p7 | 11:67258324 | AGTCTCGCTCTGTCG[C/T]CCAGGCTGGAGTGCA | 22992 |
rs574252244 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67232721 | ATTAATTAATTAATT[A/T]ATTTGAGACGGAGTC | 22992 |
rs574262266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67225675 | CTCGGGAGGCTGAGG[C/T]AGGAAAATCGCTTGA | 22992 |
rs574280044 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67241866 | CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 22992 |
rs574315922 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67216967 | CATGAGGTCTTGTCC[A/G]GGCACAGTGGCTCAC | 22992 |
rs574333571 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67227293 | CACGGTCTGAGAGTG[A/G]GTCTCTAGTCAAACT | 22992 |
rs574344403 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67241090 | AAAGTGGAAAGTCCC[A/C]GTTTGTGGACAGCTC | 22992 |
rs574352277 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67216430 | TAAACAGGTTTTGAA[A/G]GATTATCTTTATTCA | 22992 |
rs574408258 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67175210 | TGTTATAGAAGCTTA[C/T]TTTGACTAGGGTTTA | 22992 |
rs574438277 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67147154 | CACTGTTGTTGACAG[G/T]TTGGTGTAAGAGAAT | 22992 |
rs574450931 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67194824 | GCAGCAGGGTTTTAG[C/G]AGGATCCTATTTGTG | 22992 |
rs574470021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67223517 | AAGTGATCCTTCTGC[C/T]TCAGCCTCCTGAGTA | 22992 |
rs574477607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67155216 | AGATGGGGTTTTGCT[A/G]TGTTGGCCAGGCTGG | 22992 |
rs574479754 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67241742 | GATTCCATTATACTA[-/G]GAAGATTTGGGTTTC | 22992 |
rs574485299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67194373 | CAACCTTGGTAACTC[A/G]GATAAAAGTCTTTCT | 22992 |
rs574508752 | in-del | -/TC | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206427 | GACACAGCGAGACTG[-/TC]TCAAAATAAAATTAA | 22992 |
rs574570139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67207841 | AGCAGCCGGGGCAAC[A/G]TGGTGAAACCACATC | 22992 |
rs574578485 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255329 | CCTGCTCGCTTACTC[A/G]CCTGCCAGGAGGCCG | 22992 |
rs574591783 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67123721 | CACTCTTGTCACCCA[G/T]GCTGGTGTCCAATGG | 22992 |
rs574617172 | in-del | -/TTTGTTTTGT | 0.00446155 | 0.0470199 | intron-variant | KDM2A | GRCh38.p7 | 11:67198760 | AGTGGTGATCAGTAG[-/TTTGTTTTGT]TTTGTTTTGTTTTGT | 22992 |
rs574673207 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67161668 | TTAAGATGATCTGGA[A/C]AAGTGGTTCTCAACA | 22992 |
rs574677311 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67156937 | CCACAAATAAACTCG[C/T]GCTCATTCATTTAAC | 22992 |
rs574677409 | snp | A/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67121042 | TCGTCTAGGCCTCCG[A/G]CAGTTGTAATGTGAT | 22992 |
rs574692939 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67191582 | TAACAGTGAAGGAGG[A/G]AAAAAGTTACATGAT | 22992 |
rs574696805 | snp | C/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67184857 | CAAAAACAAAACACA[C/T]AATAATAAAACACAA | 22992 |
rs574700420 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67181517 | AATAATTTCCCACTT[C/T]GTTTTAAAAGTATAT | 22992 |
rs574704541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67125285 | TCCTGGTCTCGAGTG[A/G]TCTTCCCACGTCAGC | 22992 |
rs574716765 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67154082 | AGAATTTTCCAATGT[C/T]CTAAATAAAATTTTA | 22992 |
rs574733096 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | KDM2A | GRCh38.p7 | 11:67224061 | TATGAAAAGTACATC[-/T]CCTCTCCTGCCTTGC | 22992 |
rs574750747 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67124325 | TATTTTTATATATAT[A/T]TTTTGAAATGGAGAC | 22992 |
rs574760770 | in-del | -/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67222609 | TCCCAGACGGGGTGG[-/C]TGGCCGGGCAGAGGG | 22992 |
rs574761442 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67231167 | TATGTTGCCCAGGCT[A/T]AAACTATTTTTTAAA | 22992 |
rs574777567 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KDM2A | GRCh38.p7 | 11:67177089 | ATGGCGAAACCCTGT[C/T]TCTACAAAAATACAA | 22992 |
rs574782789 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67199690 | TTTAAGAAACCATCT[A/T]TGTAACAATGAAGTG | 22992 |
rs574785596 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67216885 | AGATCGCGCCATTGC[A/C]CTCTAGCCTGGGCAA | 22992 |
rs574786180 | snp | A/G | | | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67238069 | ACTCAGTTATGAGGC[A/G]TATATGCTTAAAGTT | 22992 |
rs574840899 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67168241 | GTATCTATGGTCTTT[C/G]GAACTTGGTAGATGT | 22992 |
rs574841064 | snp | G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67238717 | CCTGGAAATAAATAA[G/T]AATGCTTAAGAGCTA | 22992 |
rs574842247 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67239966 | TTGCTGAACACACCC[C/T]CTCCCGGCTCTGCAG | 22992 |
rs574856894 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67168340 | CCCTCTGTGTTAGTT[A/G]TTCTTCCTACTGGGC | 22992 |
rs574880811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67159625 | AATGGTACATTTTGC[C/T]ATTTGCAACTAGTAA | 22992 |
rs574959272 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67131311 | CCTGGGTGACAAGAG[C/T]GAAACTCCGTCTCAA | 22992 |
rs574976542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67145721 | TTACTTGAAAATGAT[A/G]CCATACTCGGCTACT | 22992 |
rs574983888 | snp | A/G | | | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67239718 | GGTGACCCTGAGGGG[A/G]AGGGTGTGGACTGAA | 22992 |
rs574994458 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67145326 | CCCGTCTACAAAAAA[A/C]ACACACACACAAAAT | 22992 |
rs575022264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67139268 | TTTTTCTTTTGAGAC[A/G]GAGTCTCGCTTTGTC | 22992 |
rs575032827 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67152388 | TTGCGAGGCTGAGGT[C/T]GGAGGGTCGTTTGAG | 22992 |
rs575041462 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67153297 | CTGGTGTGTCTTAAT[A/G]TGCATGTTTACAAGG | 22992 |
rs575065756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206256 | GCCAACATGGCAAAA[C/T]GCTGACTTTACCAAA | 22992 |
rs575086773 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67138567 | GGGCAGATCAGCAGA[A/G]GTCAGGAGTTCGAGA | 22992 |
rs575165830 | in-del | -/TTTTTTTTTT | 0.324619 | 0.238604 | intron-variant | KDM2A | GRCh38.p7 | 11:67123276 | GCCACAGTACCTGGC[-/TTTTTTTTTT]TTTTTTTTTTTTTTT | 22992 |
rs575184174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67144399 | CTGGGATTACAGGCA[C/T]GCACCACCATGCCTG | 22992 |
rs575184296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67136521 | GGTCTTCTAAATGCT[A/G]TGGTTTCAGATAATG | 22992 |
rs575194766 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67152037 | AATTAATTTCCCGCC[A/G]GGTGCAGTGGCTCAC | 22992 |
rs575197336 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67188089 | GTTGCATGCCTGTGC[C/T]CCTAGCCACTTGGAA | 22992 |
rs575202598 | snp | A/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206683 | GGGAGGTTGCAGTGA[A/G]CCGAGAGCGTGCCAC | 22992 |
rs575222612 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67158794 | GCCCCCAGCCTGAGC[A/T]TCTTTTCATATGCTT | 22992 |
rs575229006 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255115 | CTCCCCACCGAGGAG[A/G]GCCTCTCCTCGACCC | 22992 |
rs575260595 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67214144 | CTCCTGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 22992 |
rs575264495 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67227836 | TGGGCCTCCCAAGTA[C/T]CCTTTATCTTCAGTG | 22992 |
rs575270151 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | KDM2A | GRCh38.p7 | 11:67122643 | CTATTTTTTATTTAT[A/T]TTTATTTATTTATTT | 22992 |
rs575281380 | snp | C/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185505 | ATGGTGGTGGGCCCC[C/T]GTAATCCCAGCTACT | 22992 |
rs575296187 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67175128 | CCTATAGCAGAGATT[G/T]TGTTATTGCCTACTG | 22992 |
rs575336715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67129460 | CGGGCATAGGCCGGG[C/T]GCGGTGGCTCACACC | 22992 |
rs575369732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67222634 | AGAGGGGCTCCTCAC[C/T]TCCCAGTAGGGGCGG | 22992 |
rs575373982 | in-del | -/C | 0.0023933 | 0.0345097 | upstream-variant-2KB, utr-variant-3-prime | KDM2A, LOC107984341 | GRCh38.p7 | 11:67117487 | TTTTACCTTGGAGTT[-/C]CAAGCCTTGATAGAA | 22992 |
rs575391141 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67183023 | CCTTGTTAGACTACC[C/G]ACTCTTCTGTTCATC | 22992 |
rs575421681 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67236550 | ATATATCTGGCGGCC[A/C]AGCTCACTTAATAAA | 22992 |
rs575429053 | in-del | -/AGG | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67157219 | TCAGGAGGCTGAGGC[-/AGG]AGAATGGCATGAACC | 22992 |
rs575458226 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67229788 | GGCAGGAGAATCACT[A/T]GAACCCGGGAGGTGG | 22992 |
rs575460129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67221553 | GAGTTACGTATCACT[A/G]TACACATCATTGATA | 22992 |
rs575493371 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67219750 | AGAGACTTGGTCTCA[C/G/T]TGCGTTGCCCAGGCT | 22992 |
rs575504828 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67235913 | GTGAGCCACTGCGCC[C/T]GGCCAAGATATCCTT | 22992 |
rs575517668 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67157087 | GGGAGGCCGAGAAGG[A/G]CCGATCACGAGGTCA | 22992 |
rs575562599 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67189794 | GCAGTGAGCCAAGAT[A/C]GCACATTGCACTCCA | 22992 |
rs575589970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67190382 | ACCACTGCACTCCAG[C/T]CTGGGTGACAAGAGC | 22992 |
rs575612793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67150317 | TGACAAGTAAAAAAT[A/G]ATGTTTTCTTTTCTC | 22992 |
rs575619510 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67226647 | GAATGGTGTGAACCC[A/G]GGAGGTGGAGCTTGC | 22992 |
rs575677487 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67198583 | GGCGCAGTGGCGGGC[G/T]CCTGTAGTCCCAGCT | 22992 |
rs575677800 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67154254 | CCAATAAGAATGGTT[C/T]TTACGTCTTTTAATA | 22992 |
rs575684304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67212975 | AGGAAAGAAAGGCAT[C/T]CAGGGCTTATTCAAT | 22992 |
rs575693187 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67149575 | TAACCCCTTCACCAG[A/G]TGTAATCATTTTATT | 22992 |
rs575798808 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67196036 | ATTTCTCTCACTTAG[A/T]TGTAATCTTTTTATT | 22992 |
rs575816805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67212366 | ACATGCCTGTTATAG[A/G]AGCTAGCATAAAGTA | 22992 |
rs575835658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67195363 | GATCGAGTGAGACTC[C/T]GTCTCCAAAAAAAAA | 22992 |
rs575835890 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67203060 | GAAAAAGAAGTTGCT[A/G]TATCCACCCCAACCT | 22992 |
rs575836110 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67204047 | CTCAAGTGATCTGCC[C/G]GCCTCGGCCTCCCAA | 22992 |
rs575873506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67127934 | TGGTTTCAAACTCCC[A/G]ACCTCAGGCAGGCGA | 22992 |
rs575923068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67202439 | TCTCTTTGTGAAAGG[A/G]AGTATCAATCCATGT | 22992 |
rs575933919 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67234824 | CACCACTGCACTCCA[C/G/T]TCTGGGCAAAAGAGT | 22992 |
rs575936777 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67164691 | AGTGGCACAATCTCG[G/T]CTCACGGCAACCTCC | 22992 |
rs575937910 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67135097 | CCCTGAGACGGAGTT[C/T]CACTTTTGTTGCCCA | 22992 |
rs576021107 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KDM2A | GRCh38.p7 | 11:67148909 | CAAAAGAGCTGGGGT[A/G]GGGGCTGGTGGCGCA | 22992 |
rs576021755 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67172716 | TAGTTTTACTTGTTC[C/G]TTTCCAAACTTTTCT | 22992 |
rs576026570 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67243903 | TTCAGTTTAGATCCT[G/T]TATAATTTTTTTCCC | 22992 |
rs576060275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67171920 | TCCTTAAACACCAGT[A/G]CCACCCAGTCTTGAT | 22992 |
rs576068268 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67188038 | TGTCTATAAAAAAAA[A/T]AATAATAGTAATTTT | 22992 |
rs576075346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67170538 | CTGCCTGAGCCTCCC[A/G]AGTAGCTGGGACTGC | 22992 |
rs576079796 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67146545 | ACAGGGTCTCACTTT[C/G]TTATCCACGCTGGAG | 22992 |
rs576112397 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67179162 | CTAATGAGAATTGAG[C/G]ATTTTTCATGTGCTT | 22992 |
rs576118166 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67177176 | GAGGCTGAGGCGAGA[A/G]AATCACTTGAACCCG | 22992 |
rs576143337 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67169941 | TTTTGTATTTTTAGT[A/G]GAGATGGGGTTTCAC | 22992 |
rs576152961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67242156 | GGCATTTTCTCACTG[C/T]AGCATTGTTCGTAAG | 22992 |
rs576193971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67156763 | GCATGGTGGCATGTG[C/T]CTGTAATCCCAGCTA | 22992 |
rs576270495 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67177687 | ACCTCCCTGAGGCTG[G/T]TTTACAGTTAATATT | 22992 |
rs576280287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67141354 | AGGTCCTCCTCTCAA[A/G]CTATTTTGAAATATA | 22992 |
rs576282541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67140378 | CTCAAAAAAAAAATA[C/T]CATGGTTTTATACAA | 22992 |
rs576341779 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67139896 | TATTTTTTTAGTAGA[C/G]TCCGGGTTTCACTGT | 22992 |
rs576354729 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67213916 | GTTGCCCAAGCTGGA[C/G]TGCAGTGGTGATCGT | 22992 |
rs576380380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67208663 | GTAATTCCAGCTACT[C/T]GGGAGGCTGAGGCAT | 22992 |
rs576387293 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67249583 | GTGGGATTCCTCACC[A/G]TAATCCTGAGTGAAT | 22992 |
rs576390965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67210651 | AATACTAATATCTTA[C/T]GGGGACCTAAAACAT | 22992 |
rs576407075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67161843 | AACTATATCATGTGT[A/G]ATGATAATGCTCTCA | 22992 |
rs576427236 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67126424 | CACACAGATTGTTTT[C/T]TGGCCGGGTGCGGTT | 22992 |
rs576428740 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67146376 | TTTTTATAGATCCTG[A/T]GGGCAAAAATCATGG | 22992 |
rs576469290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67145883 | CATCCTTTGGGAATT[C/T]TTTTTTTTTTAATTC | 22992 |
rs576568785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67133046 | ACTTAATTGGGGATG[C/T]TGAGCCTTGAGTTTT | 22992 |
rs576611495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67132423 | CAAGTAGCTGGGATT[A/G]CAGGCACGTGCCACC | 22992 |
rs576618954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | KDM2A | GRCh38.p7 | 11:67186430 | TCCTTCAAAAGGGGC[A/G]AGAGATTAAGACATT | 22992 |
rs576658045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67225025 | TATTTCTAGTAGAGA[C/T]GGGGTTTCAGCAGGC | 22992 |
rs576671412 | snp | G/T | 0.000399281 | 0.0141238 | synonymous-codon, intron-variant | KDM2A | GRCh38.p7 | 11:67240219 | CCCTATGTGCTCTGG[G/T]AGATTCCAGAATATT | 22992 |
rs576681001 | snp | C/G | 1.71064e-05 | 0.00292454 | missense, intron-variant | KDM2A | GRCh38.p7 | 11:67250619 | GGAAGAGGAGGAGGA[C/G]GAGGAGGAAGATGAC | 22992 |
rs576683797 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67169828 | AGTGGCGAGATCTCG[G/T]CTCACTGCAACCTCT | 22992 |
rs576693771 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67124294 | CAGGTGTGAGCCACC[A/G]TGCCCGGCTTCACTT | 22992 |
rs576732731 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67193309 | CTTAAACTTTCAACA[A/G]TCTGATGGGTATGAA | 22992 |
rs576756982 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67249946 | AGACCAGCCTGGGCC[A/G]ACTCTGAGGGAATGA | 22992 |
rs576757680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67123772 | ACCTCTTCCTCCTGG[A/G]TTCAAGTGATTCTCT | 22992 |
rs576784644 | snp | C/T | 0.000773208 | 0.019647 | intron-variant | KDM2A | GRCh38.p7 | 11:67231555 | ACTGCATTTTTTCTT[C/T]ATATTGGTAGATTTG | 22992 |
rs576808041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67229866 | CAGAGTGAGACTCCG[C/T]CTCAAAAAGAAAAAA | 22992 |
rs576812831 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67238510 | TTAAGATACAGTGTC[C/T]GGGAGAAGTTTAGGG | 22992 |
rs576836097 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67120676 | TAGATTTGGGAATGA[C/T]AAGATCCGGGGAGTC | 22992 |
rs576869528 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67171838 | ATGCTTACTGAAAAT[-/C]AATTCACTGTAAGTG | 22992 |
rs576876808 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67201677 | GGAGGCTGAAGCAGG[A/C]GAATCACTTGAACCT | 22992 |
rs576896314 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67161118 | TGTATTCCCCACACT[G/T]TGGGAGGCCAAGTTG | 22992 |
rs576901129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67237306 | TTGTTGCAAATAACT[C/T]CAGAAATACTAATTA | 22992 |
rs576911924 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67201086 | GTAGTCCCAGCTACT[C/G]GGGAGGCTGAGGCAG | 22992 |
rs576954280 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67150361 | ATTTACCACCACCTT[G/T]TTGGGCCAAAGGAGA | 22992 |
rs576957543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67199673 | GAGGTTGGTTTATGA[A/G]GTTTAAGAAACCATC | 22992 |
rs577007352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67207804 | CCAAGGGAGGCAGAT[C/T]GCTTGAGCTGAGGAG | 22992 |
rs577020261 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67223376 | ATTTCATATTTTCTT[A/C]CTTTTTTCTTTCTTA | 22992 |
rs577029088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67198824 | CACTCTGTTGCCCAG[A/G]CTGGAATGCAGTGGC | 22992 |
rs577042189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206082 | ATTCTCCACAAGATA[C/T]TAATGTTCAGAGAAA | 22992 |
rs577044873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206900 | CCTGGTGTCTTTATC[A/G]TTCTATAAATATTTG | 22992 |
rs577067431 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67147796 | GATTCTCCAGCCTCA[A/G/T]CCTTCCAAGTAGCTG | 22992 |
rs577073452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67168842 | GAGAGCAGAGTGAAA[A/G]CCTGAGGTTGCTTTT | 22992 |
rs577081711 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67216804 | ACATGCCTATAATCC[C/T]AGCTACTCGGGAGGC | 22992 |
rs577091771 | in-del | -/CAA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67233667 | CAACAACAACAACAA[-/CAA]ATCCATTGGAGTAGT | 22992 |
rs577094449 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | KDM2A | GRCh38.p7 | 11:67126601 | TAGTCCCAGCTACTC[A/G]GGAGGCTCAGACAGG | 22992 |
rs577099375 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67131114 | CAGATTGCCTGAGGT[C/G]AGGAGTTCAAGACCA | 22992 |
rs577114697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67205553 | ACACCTCACCCTCCC[A/G]AGTAGCCGGGATTAC | 22992 |
rs577136584 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67181155 | GCTCTCCATATTTTC[G/T]AAGAGATGCTTCTTA | 22992 |
rs577140271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67184544 | GAGGCAGGAGAATTG[C/T]TTGAACCGGGAGGCA | 22992 |
rs577157458 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67168053 | ACTTCCTTAGGGCAT[G/T]TTAATTAAAATCCAT | 22992 |
rs577177926 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67184002 | TAGTCCCAGCTACGT[C/G]GGGGGCAATTCCTTG | 22992 |
rs577193299 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67176952 | TTTTTAATTTATAAA[A/T]TTTTTTTTTTCAATA | 22992 |
rs577208560 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67172419 | TCATGAACACAGGAC[A/G]TTTTTCTATTTAGCT | 22992 |
rs577212113 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67250927 | GTGAATTGACCCTTT[C/T]TCCCAAACTTTGGGT | 22992 |
rs577223991 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67177359 | CTAATTTTCCACTTT[C/T]GTAATAATACTTAGC | 22992 |
rs577246147 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67207978 | TGAGGCTGCAGTGAC[C/T]GGTGATTGCACCACT | 22992 |
rs577261208 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67214093 | TTTCCCAGGCTGGAG[G/T]GCAGTGGCACCATCT | 22992 |
rs577262086 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67191485 | CAGCAGCATATTAAA[A/C]GGATTATACACCATG | 22992 |
rs577281965 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67176229 | TTTCCTCTGGTATGT[A/G]ATAGTCAAGTTTATT | 22992 |
rs577364866 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255752 | TCCTTATTGCACTTA[C/T]TGGGGTTGAAGCTCT | 22992 |
rs577387498 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67182132 | ATACTTCCTTCTCTC[C/G]TTGAAGAGTGTGCCT | 22992 |
rs577399845 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255281 | AGTAGCAGATTGATC[G/T]GAGGGGAAAGCACAG | 22992 |
rs577431098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67145171 | GCCACCGTGCCCGAC[C/T]ATTCACATGGTTTTT | 22992 |
rs577446265 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67204975 | AATATTTATGTACAA[A/G]CTTTTGTTTGAACAC | 22992 |
rs577469368 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67142283 | CTCAGGTGATCCACC[C/T]GCCTTGGCCTCCCAA | 22992 |
rs577485046 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67186219 | CAAACTTTCAAAAGC[A/C]AAAGACAAACTCTTG | 22992 |
rs577510233 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67152268 | CAGTGAGCCGAGATT[A/G]CACCACTGCACTCCA | 22992 |
rs577527580 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67166292 | TGGGTTCAAGTGATT[C/G]TCGTGCCTCAGCCTC | 22992 |
rs577548817 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67151748 | TATTATTATTTCTTA[C/T]TTTTTTATTTTTATA | 22992 |
rs577553689 | snp | A/G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67138123 | TATTATAGGACCACC[A/G/T]TCACATATACAGTTG | 22992 |
rs577585967 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67221450 | TATGAATGGTCTTTT[A/T]TATATTATAGGAATG | 22992 |
rs577616959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67165881 | TTACGGTCAACTTTT[A/G]GGGGTTTTTTCTTTT | 22992 |
rs577649254 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67148604 | TCAGGAGTTTGAGAC[C/T]AGCCTGGCTAACATG | 22992 |
rs577649359 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67157436 | TAAAAGCAAAAAAAT[A/T]CCTGGTTTCTCTTAT | 22992 |
rs577660484 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67230647 | AACAAACCACAACAT[-/A]AAAAAAAAAAACCCA | 22992 |
rs577768789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67189671 | ATGGCGAAACCCCAT[C/T]TCTACTAAAAATACA | 22992 |
rs577771609 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67228860 | CCCTCCTGAGTAACT[A/G]GGATTACAAGCACAC | 22992 |
rs577779940 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67121935 | ACGAGATAGATCTTG[A/T]TGAAAGAAATTTTAG | 22992 |
rs577833575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67244915 | GGCGGGAACCCGGGA[A/G]GCGGAGCTTGCAGTG | 22992 |
rs577856239 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67197644 | TCAGAAAGAAGTAAG[C/G]CATTCTGTCTTGTAA | 22992 |
rs577859668 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67228260 | CAATATGTTCTTGGT[A/T]TTTTAATTCATCTAC | 22992 |
rs577865380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67189006 | TCTCAATAATGGATA[A/G]AACAACCAGACAGAA | 22992 |
rs577881403 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | KDM2A, LOC107984341 | GRCh38.p7 | 11:67119263 | GGAGGAGCTGTGTGT[A/G]TGTGAGAGTCTGACG | 22992 |
rs577887699 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67127239 | TGGGACTACAGGCAT[A/G]CATGTGCCACCATGC | 22992 |
rs577901363 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67196974 | TAAGATCTTATTCAG[C/T]CATCAGTCTTCGGTT | 22992 |
rs577904914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67128062 | CTCTGTTGCCCAGGC[C/T]GGAGTGCAATGGCAC | 22992 |
rs577947364 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67126587 | GTGGCAGGCGCCTGT[A/C]GTCCCAGCTACTCAG | 22992 |
rs577977238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67235018 | GGTGTCTTGGCGGGC[A/G]CCTGTATTCCCAGCT | 22992 |
rs578007460 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67244274 | CTTGTCCTTGAAAAG[A/G]TCACCAGCAGGGTAA | 22992 |
rs578068501 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67219607 | TTTTCCAGGCTAGAG[G/T]GCAGTGGCGTGATCA | 22992 |
rs578091788 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67163468 | TTAATGCCATTGGAG[A/T]AGAGGCAAGTATGAC | 22992 |
rs578093726 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67163426 | GACTTGGAAAATTCT[A/G]TGACTTGGAATGATA | 22992 |
rs578111059 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67212074 | GCTGTGGTGGGAGAA[G/T]TGCTTGAGCCCAGGA | 22992 |
rs578112410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67203269 | TAGCCTACAGTATAA[C/T]GTAAATATATGCACT | 22992 |
rs578160660 | in-del | -/GTG | 0.00557542 | 0.0525036 | intron-variant | KDM2A | GRCh38.p7 | 11:67156958 | TTCATTTAACATGTT[-/GTG]GTAGAGGCTGTATGG | 22992 |
rs578174968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67210982 | GAATCACTTGAACCC[A/G]GGAGGCAGAAGTTGC | 22992 |
rs578236742 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67196687 | AACCAAAATCATGGA[C/G]ACAAAATAGAATAGT | 22992 |
rs578246763 | snp | A/C | 1.6853e-05 | 0.0029028 | intron-variant | KDM2A | GRCh38.p7 | 11:67180054 | AAAGTGCATGATTTC[A/C]TCAGTATGTTCCTTT | 22992 |
rs578253877 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67193690 | CATGGCAAAACGCCG[-/T]TATCTACTAAAAATA | 22992 |
rs745310046 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67212332 | AAGTAGGTTCCGGGA[A/G]GTAAGAAGGGCAACT | 22992 |
rs745316900 | snp | A/G | 1.96088e-05 | 0.00313114 | missense, nc-transcript-variant, utr-variant-5-prime | KDM2A | GRCh38.p7 | 11:67217855 | AGCGCATTGAGCTCA[A/G]GCAGGGCTATACCTT | 22992 |
rs745348986 | in-del | -/GTGTGTGTGTG | | | intron-variant | KDM2A | GRCh38.p7 | 11:67152942 | TGTGTGTGTGTGTGT[-/GTGTGTGTGTG]TTTTCAGGAATTCCT | 22992 |
rs745360472 | snp | C/T | | | missense, intron-variant | KDM2A | GRCh38.p7 | 11:67250564 | GCCCAGCCCGAACCC[C/T]CCAGCGTGGGGATGA | 22992 |
rs745370619 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67135356 | AGCGTGAGCCACCGC[A/G]CCCAGCACAGATTTC | 22992 |
rs745401176 | snp | A/T | 2.6078e-05 | 0.00361086 | intron-variant | KDM2A | GRCh38.p7 | 11:67219273 | AGCCACTGCCCTCTG[A/T]TCCCCTTCTCCTAGG | 22992 |
rs745403669 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67227468 | TGTGTCTTACTCTTA[C/T]ATTTTACTCTGTCCC | 22992 |
rs745459460 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67148018 | TCTCTAGCTGATCAT[C/G]TAGTGGTAATGTAAA | 22992 |
rs745475142 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67251451 | GATGATGAACAAGGA[C/G]CTTCCCATTGGGCAT | 22992 |
rs745503626 | snp | A/G | 3.31499e-05 | 0.0040711 | synonymous-codon, intron-variant | KDM2A | GRCh38.p7 | 11:67250439 | CCTCACTGTCACGCT[A/G]CAGAGGCCCACCAAA | 22992 |
rs745508755 | snp | C/G | 1.65861e-05 | 0.00287972 | intron-variant | KDM2A | GRCh38.p7 | 11:67121370 | ATTGGTTAGTATTTT[C/G]TCCCCCCACCACACC | 22992 |
rs745535292 | in-del | -/AT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67188830 | TCAAGAGGCAAAGAC[-/AT]ATATTAATTAAAGGT | 22992 |
rs745565299 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67196489 | CTAAATGTCCATCAG[C/T]AGTGAATACTTTAGC | 22992 |
rs745593523 | snp | A/G | 5.09862e-05 | 0.00504881 | missense, intron-variant | KDM2A | GRCh38.p7 | 11:67250558 | AGCACTGCCCAGCCC[A/G]AACCCCCCAGCGTGG | 22992 |
rs745594575 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67213338 | TCATGGTGGTTTGGC[C/T]CTCGAGTTTTACCTA | 22992 |
rs745609437 | snp | A/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67184824 | CCTTGACACAGAGAT[A/G]GCCTATAAAAAACAA | 22992 |
rs745634679 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67123257 | CTGGGATTAACAAGC[G/T]TGAGCCACAGTACCT | 22992 |
rs745644886 | snp | C/G | | | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67238341 | GTTTTAAAGTAATAT[C/G]TTTTCTCTTAAGTAT | 22992 |
rs745671630 | snp | C/T | 1.83687e-05 | 0.00303051 | intron-variant | KDM2A | GRCh38.p7 | 11:67232009 | ATCCAGCTATGGCAG[C/T]CAGCTTCCAGATTCA | 22992 |
rs745672317 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67218889 | GCTGGGATTATAGGC[A/G]TGAGCCCCCGCGCCA | 22992 |
rs745685606 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67149224 | TTGGTGGAGTCCCTT[C/T]CAGGTTCTAACATTT | 22992 |
rs745735023 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67156901 | TCTCAAAAAGAAAAT[A/G]TGAAATAGGAGCTTC | 22992 |
rs745757617 | snp | G/T | 3.36615e-05 | 0.00410239 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67207517 | TATGGCAGGGAGTCG[G/T]CGCATGGTGGATGTC | 22992 |
rs745771076 | snp | A/G | | | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67238322 | GCAACTTGAACTTAC[A/G]TTTGTTTTAAAGTAA | 22992 |
rs745776125 | in-del | -/TT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67168953 | TTTAATCCATGTAGT[-/TT]TTTTTTTTTTTTTTT | 22992 |
rs745787325 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67172085 | GCCTCAACCTCCGGG[A/C]CTCAAGCCATCCTTC | 22992 |
rs745805672 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67171181 | TTTAACATCTGTTTG[A/G]TTGAGATTTGTGATA | 22992 |
rs745810676 | snp | A/C | 1.66815e-05 | 0.00288799 | intron-variant | KDM2A | GRCh38.p7 | 11:67253436 | TATTATTACATGTCT[A/C]ATTCCATCCATTGCA | 22992 |
rs745821346 | in-del | -/A/AA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67195378 | GTCTCCAAAAAAAAA[-/A/AA]AAAAAAAAAAAAAAA | 22992 |
rs745837104 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67134707 | ACAGGATTTCGCCAC[A/G]TTGACTAGGCTGGTC | 22992 |
rs745863257 | in-del | -/AGT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67147660 | TTTCTCTGGAGACTG[-/AGT]AGTTCCCTTTCATTA | 22992 |
rs745872538 | snp | C/T | 1.68202e-05 | 0.00289996 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | KDM2A | GRCh38.p7 | 11:67215363 | CATTGACTGGGTAGA[C/T]AACATGTGGCCAAGG | 22992 |
rs745893002 | snp | C/T | 1.68422e-05 | 0.00290187 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67250195 | ATTCACCCACTTCCA[C/T]GCTGCAGCTCATCCA | 22992 |
rs745893911 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67207727 | ATTGTCATTGTCACC[A/T]AAAGGGTTGTTTTCG | 22992 |
rs745894135 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67192188 | CTTCCCATTTTCAAT[C/G]CCTTTTCCTTCCTCC | 22992 |
rs745950972 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67244562 | AGAAAGGGAAGCAGC[C/T]GAATTAGTAGGCCAA | 22992 |
rs745964890 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67141383 | TACAATTCATTGTTA[C/T]TGGCCGGGCGCGGTG | 22992 |
rs745967441 | snp | C/T | 1.66891e-05 | 0.00288864 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67250299 | AGCCGCGATGAGCGC[C/T]TCAAACGGCGGCAGT | 22992 |
rs745978847 | snp | A/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206716 | CACTCCAGCCTGAGC[A/G]ACAGAGCGAGACTCC | 22992 |
rs745980372 | snp | A/G | 4.3306e-05 | 0.00465308 | intron-variant | KDM2A | GRCh38.p7 | 11:67231561 | TTTTTTCTTCATATT[A/G]GTAGATTTGGAGTTA | 22992 |
rs745990566 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67158259 | CTTTGTGGCTACATA[C/T]CTCATTTCTTTGTAT | 22992 |
rs746000068 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67205132 | CCAGTAGATGTATGA[A/G]GGTTCCAATTTCTCT | 22992 |
rs746050248 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67141404 | GGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 22992 |
rs746056503 | snp | A/G | 1.98762e-05 | 0.00315241 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67181347 | AGTATATTCAGCGGG[A/G]TGGCTTGAGAGATCC | 22992 |
rs746057378 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67179805 | TTTAGTAGACCCTCT[G/T]TGGTCCTGTTTTTAT | 22992 |
rs746075649 | snp | C/T | 2.0646e-05 | 0.00321288 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67231633 | TCGAGAACCCCGACG[C/T]TTGAGCAGCAGGCGT | 22992 |
rs746089205 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67129063 | ACTCCAGCTTGGGCT[A/G]CAGAGCAAGACCCTG | 22992 |
rs746155293 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67193569 | TTATCCTTTTAAATA[A/C]GTATATATTGGCTGG | 22992 |
rs746171031 | snp | A/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67178495 | TCTAATTCCAGAACA[A/T]TTTCATTGCTCTTGA | 22992 |
rs746180804 | snp | A/G | 0.000178763 | 0.00945249 | intron-variant | KDM2A | GRCh38.p7 | 11:67252624 | CTTTTCCCAGAAGCC[A/G]TAAGCAGCCTGTGAT | 22992 |
rs746256351 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67234027 | CAGCTTCTCGTTTAC[C/G]CAAAACCACAGTCAA | 22992 |
rs746258299 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67215591 | GACTTTACAGTTCCA[C/T]AAGGAAGAGTGTATG | 22992 |
rs746270365 | in-del | -/TATTA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67137393 | GATTAATTAGGAGGC[-/TATTA]TATTGGTTCAGGTAA | 22992 |
rs746280760 | snp | A/G | 3.31686e-05 | 0.00407225 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67245239 | TACCATCCCCATTAC[A/G]AAGCCTCACACTATG | 22992 |
rs746293805 | snp | A/G | 1.66305e-05 | 0.00288357 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67252788 | ATCAAGAGGCAGCCA[A/G]TCAGCCTTGACCTCA | 22992 |
rs746307297 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67136761 | GTAGGAATGAGAAAA[C/T]AATACTAAGCATTTA | 22992 |
rs746325675 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67160248 | GAGTTTGTCTTTGTA[A/G]CCTCGAGGGATCATT | 22992 |
rs746330826 | in-del | -/TTCC | 3.3592e-05 | 0.00409815 | intron-variant | KDM2A | GRCh38.p7 | 11:67180063 | GATTTCATCAGTATG[-/TTCC]TTTCTTTCCTAGCGT | 22992 |
rs746359024 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67187214 | AATGTATCTAAGTAC[A/G]AAAGAAAACAGTAAT | 22992 |
rs746370877 | snp | A/G | 1.65982e-05 | 0.00288077 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67245419 | GTTTGGGGGGCCTGG[A/G]CGCATGAAGCAGTCC | 22992 |
rs746378518 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67227189 | ATCTGGTTTGTGGAC[A/G]TACCATTTTGGCAGA | 22992 |
rs746378696 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67189209 | TAGATATCAAAGTAT[A/C]TTCTCCAACCACAAT | 22992 |
rs746416505 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255557 | GGCCAGCAGCCCCAG[A/G]AGTCCCAGACCCGTG | 22992 |
rs746418808 | in-del | -/TTTCTCTTTCCA | 1.66863e-05 | 0.0028884 | cds-indel, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67245455 | CTCCGACAGTGCTTG[-/TTTCTCTTTCCA]GCAGTGAGTGATCTG | 22992 |
rs746428583 | snp | C/T | | | utr-variant-5-prime, intron-variant | KDM2A | GRCh38.p7 | 11:67240204 | AGCTGGACTGCCCTG[C/T]CCTATGTGCTCTGGG | 22992 |
rs746435910 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67151784 | AGGGTTTCACTCTTA[A/C]CCAGACTGGAGTGTA | 22992 |
rs746444655 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67166848 | TTGGAAGGCCAAGGC[A/G]GGCGGATCACTTGAG | 22992 |
rs746457826 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67189109 | AACAGCAATAGCATA[C/G]ACATTCTTTTCAAGT | 22992 |
rs746514449 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67131390 | CTTTCTCTCTTTTGA[A/G]GCTACTTTAGTGTTT | 22992 |
rs746521296 | snp | C/T | 1.65712e-05 | 0.00287843 | intron-variant | KDM2A | GRCh38.p7 | 11:67215991 | GGAATCTGAAGTTGG[C/T]TGTATGACTTTGCTT | 22992 |
rs746538240 | snp | A/G | 1.65861e-05 | 0.00287972 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67245401 | CTGCAGAGACATGAA[A/G]AAGTTTGGGGGGCCT | 22992 |
rs746545440 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67240845 | CCAGCAAAATAAGGC[G/T]TGGAAGGAAATCTGC | 22992 |
rs746554529 | in-del | -/AG | | | intron-variant | KDM2A | GRCh38.p7 | 11:67164389 | CTGGAGAAGTTTAAC[-/AG]AGATGTGATTATTAA | 22992 |
rs746574779 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67133249 | GGATTACAGGCGTGC[A/G]CCACCACACTGCGCT | 22992 |
rs746604525 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67161414 | ATGTGCAAGCTTTTG[C/T]TTAGACAGTAGATTA | 22992 |
rs746626323 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67195323 | GCAGTGAGCCGAGAT[C/T]GCACCACTGCACTCC | 22992 |
rs746674189 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67249154 | TATTTGTCTTTGAGG[A/G]CAAGGATTTTTGAAG | 22992 |
rs746676918 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67124302 | AGCCACCGTGCCCGG[C/G]TTCACTTTATTTTTA | 22992 |
rs746685782 | snp | G/T | 0.000183286 | 0.00957128 | splice-donor-variant | KDM2A | GRCh38.p7 | 11:67254420 | GCTCAATATGGCAGG[G/T]ATGCCGCTACAGTTG | 22992 |
rs746697074 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67209961 | GTTACTCAAGAGACC[A/G]AGGTGGGAGGATTGC | 22992 |
rs746724650 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67227298 | TCTGAGAGTGAGTCT[C/G]TAGTCAAACTTTAGT | 22992 |
rs746726546 | in-del | -/GTG | | | intron-variant | KDM2A | GRCh38.p7 | 11:67202107 | GAAGTAACTGCAAAT[-/GTG]GTGAAAATAGTGAGA | 22992 |
rs746727588 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67160334 | TGCCTTTGCCGGTTT[A/G]GGAAGAGATTATAGC | 22992 |
rs746762305 | snp | G/T | 2.16932e-05 | 0.00329334 | intron-variant | KDM2A | GRCh38.p7 | 11:67254502 | TAAACCAGAATGACC[G/T]TGGGTCTGTTGATTG | 22992 |
rs746768946 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67149424 | TCTCAAAGCTTAATA[C/T]GTTATTATATATAAC | 22992 |
rs746785377 | in-del | -/AG | | | intron-variant | KDM2A | GRCh38.p7 | 11:67154306 | TAAAATTTGTGTAAC[-/AG]AAAATTAACCATTGA | 22992 |
rs746823790 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67180698 | TGCTGTGTCACCCAG[C/G]GTGGAGTGCAGTGGT | 22992 |
rs746832356 | snp | A/G | 1.65767e-05 | 0.00287891 | missense, intron-variant | KDM2A | GRCh38.p7 | 11:67250414 | AGAAAGCCAAGATCC[A/G]GGGATCGTACCTCAC | 22992 |
rs746835057 | snp | C/T | | | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67250134 | GTGCAAGCCAAAGTC[C/T]TGCGGCCCCTGCGGA | 22992 |
rs746852978 | snp | A/G | 1.75351e-05 | 0.00296095 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67231672 | CACTAGCCCTGTAGC[A/G]AATGGAGTCAACCTG | 22992 |
rs746853671 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67212136 | CCAGTCTTTTAAAAT[G/T]AAAAAAATTGAATAA | 22992 |
rs746923194 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67152377 | TTCCAAGTATTTTGC[A/G]AGGCTGAGGTTGGAG | 22992 |
rs746924785 | snp | A/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67184627 | GCGAGACTCATCTCA[A/G]AAAAAGGTGAGTGGA | 22992 |
rs746941241 | snp | A/G | 1.65655e-05 | 0.00287793 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67231795 | CCACAATGGACAAGT[A/G]TGGGATCCCCAGTGT | 22992 |
rs746996656 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67217657 | GGTCTTAATTTTGTA[C/T]CTGTTTATCAGTTGA | 22992 |
rs747026379 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67155164 | GGGTTGCAGGTGCCT[C/G]CCACCACACCCAGCT | 22992 |
rs747072499 | in-del | -/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67189813 | CATTGCACTCCAGCC[-/G]GGGCAACAAAGTGAG | 22992 |
rs747074788 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67170984 | CCTGGGCAAGTTACT[A/T]CTTTCATTTTCCTTG | 22992 |
rs747075005 | snp | G/T | 1.65787e-05 | 0.00287907 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67253592 | TCGGGACTTGCTTAC[G/T]CCACCGGCTGATAAA | 22992 |
rs747094559 | snp | A/G | | | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67119978 | AAGACGACGTTTGGG[A/G]TTTAATTATTCCTCT | 22992 |
rs747121641 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67218736 | CTGTCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 22992 |
rs747134954 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67122757 | CTCTGCTCACTGCAC[G/T]CTCCGCCTCCTGGGT | 22992 |
rs747158577 | snp | A/G | 4.54907e-05 | 0.00476899 | intron-variant | KDM2A | GRCh38.p7 | 11:67248401 | CAGATTTGCACTGTG[A/G]CAGAAAGGAGGCATC | 22992 |
rs747164117 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67141176 | AAGATACCCATCCAT[A/T]TACTTCTGTCCCTTA | 22992 |
rs747173725 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67191988 | ACACTTAGTTTTGCT[C/G]TTTGTCAAATATTTC | 22992 |
rs747194897 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67170515 | CCTCCTGGGTTCGCA[C/T]CATTCTCCTGCCTGA | 22992 |
rs747225473 | snp | A/C | 1.65608e-05 | 0.00287752 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67228104 | TGGAGCGCTATGTGT[A/C]CTGCATAACCAACCG | 22992 |
rs747284145 | snp | C/T | 1.66275e-05 | 0.00288331 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255105 | CTTCCCCTGACTCCC[C/T]ACCGAGGAGAGCCTC | 22992 |
rs747297132 | snp | A/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206566 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAATAC | 22992 |
rs747311675 | snp | A/G | 6.26743e-05 | 0.00559761 | intron-variant | KDM2A | GRCh38.p7 | 11:67231517 | TTTCTCTTGCTGATC[A/G]CATGGCAGAGTGAAA | 22992 |
rs747315705 | snp | A/G | 1.70064e-05 | 0.00291597 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67180196 | TATAATGCCAATTTT[A/G]TTACTTTTATGGAAG | 22992 |
rs747320101 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67190661 | AGCTACTCAGGAGGC[A/T]GAGTCATGAGAATCG | 22992 |
rs747334384 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67232045 | AGAAAATATAGGAAT[C/T]TTGGGTGATCTCTGG | 22992 |
rs747359370 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67229741 | CAGGCGTGGTGTTGC[A/G]CACCTGTAGTACCAG | 22992 |
rs747401008 | snp | C/T | 0.000182229 | 0.00954366 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67246113 | TCATCCTGGCTGCCT[C/T]CAGGTGAGGAGAGCT | 22992 |
rs747423145 | snp | A/G | 3.6535e-05 | 0.00427389 | missense, intron-variant | KDM2A | GRCh38.p7 | 11:67250774 | TTTGTGAATGTATGC[A/G]AGTGTGCAAGACGTG | 22992 |
rs747426860 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67186867 | GAACCCAGGAATTCA[A/G]GACCAGCCTGGGCAA | 22992 |
rs747456839 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67165833 | CTTTCTTGACTGGCA[A/G]AAAGAAAGGTCACTC | 22992 |
rs747472891 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67257824 | CTATCTCAGTTGACA[A/C]ATTGAGGTTATTTTG | 22992 |
rs747489223 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67149984 | TCCTCAGCCTCCCAA[A/G]GTGCTGGGATTACAG | 22992 |
rs747513758 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67253771 | GTGTACAAGAATAGG[A/G]TAACTATAAGCAGAT | 22992 |
rs747529775 | snp | A/C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67221653 | ATTTTATAAAAGTAC[A/C/G]TTTCTTTTTATTTGT | 22992 |
rs747582607 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67164619 | ATCACACTTGACTGC[A/T]GTTGGACTTTTTTTT | 22992 |
rs747620911 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67229091 | TAGGAATACATCATC[-/A]GAATAACCTGTTGTA | 22992 |
rs747629098 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67254696 | CATATGGTGATGGGA[C/G]TGAGGCAGCAGGGTC | 22992 |
rs747646695 | in-del | -/ATT | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67207326 | ATAATTATTATTAAC[-/ATT]ATCCATTGTCTTTCC | 22992 |
rs747664154 | snp | C/T | 3.31241e-05 | 0.00406952 | missense, nc-transcript-variant, intron-variant | KDM2A | GRCh38.p7 | 11:67243040 | TTGCCAACAGCGATC[C/T]CAAGTTAGCCCTCAC | 22992 |
rs747688453 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67151156 | GCATACGTTGCTTTA[C/G]GAGATACACATACAT | 22992 |
rs747711381 | snp | C/T | | | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67238771 | AAAAAAGGCAAGTTA[C/T]ACATTTGTAAGGGTC | 22992 |
rs747723664 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67134835 | ATCTAACACAAAACA[C/T]CTCAAAAGCAGTCTC | 22992 |
rs747740113 | snp | A/G | 8.89878e-05 | 0.00666978 | intron-variant | KDM2A | GRCh38.p7 | 11:67252592 | ACTTGTAGAAGAACG[A/G]GCCTCCAGGTACTCT | 22992 |
rs747757468 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67172699 | TAATTTGTGAATAGA[C/T]GTAGTTTTACTTGTT | 22992 |
rs747801807 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67187047 | GTAAAGGAGCAGATT[A/C]TTTGAATAGTAGTGA | 22992 |
rs747814456 | in-del | -/AA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67156720 | CGAGACTCCATCTCA[-/AA]AAAAAAAAAAAAAAA | 22992 |
rs747814662 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67137568 | TAAAGGAGGTAAATA[-/T]TAAGTATGACTCCCA | 22992 |
rs747819711 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67173649 | CCGCCCTGGCCTCCC[A/G]GAGTGCTAAGATTAC | 22992 |
rs747834472 | snp | A/G | 3.34941e-05 | 0.00409218 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67245194 | CTCTTTCCAGCTTAA[A/G]TTCCCCACTCGGCCA | 22992 |
rs747848265 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67223619 | TTTACTATGCTGCCC[A/C]GGCTCGTCTCAAACT | 22992 |
rs747858772 | snp | C/T | | | utr-variant-5-prime, intron-variant | KDM2A | GRCh38.p7 | 11:67240178 | TCCCTCTGGGTAGTC[C/T]GAAGGGTCAGAGCTG | 22992 |
rs747883856 | snp | A/G | 1.6566e-05 | 0.00287797 | intron-variant | KDM2A | GRCh38.p7 | 11:67215979 | GTGATAGGGGTTGGA[A/G]TCTGAAGTTGGTTGT | 22992 |
rs747918113 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67193856 | ACAGAGTGAGACCCC[A/G]TCTCAATACATACAT | 22992 |
rs747919104 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67131151 | CCAACATGACGAAAC[C/T]CCATCTCTACTAAAA | 22992 |
rs747931792 | snp | C/T | 1.65625e-05 | 0.00287766 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67254383 | CTGCTGTCGGGTCTT[C/T]CACTCGCTACTCTCT | 22992 |
rs747985459 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67225513 | CGCTGGCTCACGCCT[C/G]TAATCCCAGCACTTT | 22992 |
rs747989759 | in-del | -/GTT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67170387 | CCTACCAAGCATGGG[-/GTT]TTTTTTTTTTCTTTC | 22992 |
rs747997694 | snp | A/G | 1.68111e-05 | 0.00289918 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67250218 | CTCATCCATGACCCG[A/G]TTTCCCCCCGGGGTA | 22992 |
rs748010441 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67160174 | CTGAAATAAAATTCT[A/G]TAGTTCAGTTCTGTT | 22992 |
rs748026091 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67176948 | TATTTTTTAATTTAT[-/A]AAAATTTTTTTTTTC | 22992 |
rs748061377 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67180465 | GATTTTTTTGCCTAA[C/T]GGCCTCTTCCTCCTT | 22992 |
rs748091113 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67161284 | TGATCATGGTAAACT[A/G]TGACTTTTTCAATCT | 22992 |
rs748095171 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67131685 | CCAGAATGCTGAGAT[G/T]ACAGGCATGAGCCAC | 22992 |
rs748119500 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67234349 | CAGTTTACCCTTCCT[G/T]CAGAGAAAGGAATTG | 22992 |
rs748193026 | in-del | -/TGCTCAGGCTGGTCTGGTTTTTTT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67127305 | TATCCCTGTTCGGGC[-/TGCTCAGGCTGGTCTGGTTTTTTT]TGCTCAGTCTGGTCT | 22992 |
rs748198881 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67167065 | CCTAGGCGACAGAGC[A/G]AGACTCTGCCTCAAA | 22992 |
rs748212491 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255872 | CCCTCTCTCTTTTGC[C/G]TCCCACTGACTGCCC | 22992 |
rs748214871 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67183577 | TTGCAAATTTCAGGG[A/G]CAGCTTGGACAATAA | 22992 |
rs748264670 | snp | G/T | 8.3743e-05 | 0.00647028 | intron-variant | KDM2A | GRCh38.p7 | 11:67253419 | TATGCTGGGAAACAG[G/T]GTATTATTACATGTC | 22992 |
rs748267809 | snp | A/G | 0.0172038 | 0.0911368 | missense, nc-transcript-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67207512 | TCTTTTATGGCAGGG[A/G]GTCGTCGCATGGTGG | 22992 |
rs748283505 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67205464 | GGGCAGGTGTTTGTT[C/T]GTCTTACAAGGAAGA | 22992 |
rs748303853 | snp | G/T | | | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67119898 | TTTGATTCAGCAACT[G/T]TTTGCTCCCTTTTCC | 22992 |
rs748305385 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67154953 | TTTCTACCTTTTAGC[G/T]ACTGTGAATAGTGCT | 22992 |
rs748373360 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67218659 | CCTCAGGCTGGAGTG[C/T]AGTAGCGTGATCTTG | 22992 |
rs748377407 | in-del | -/TCTTGTGGTG | 9.47463e-05 | 0.00688216 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255482 | TCTCCATGGCCAGGT[-/TCTTGTGGTG]TCTTGTGGTGTCCAG | 22992 |
rs748382837 | in-del | -/AG | | | intron-variant | KDM2A | GRCh38.p7 | 11:67232551 | GCAGGTTTATTACAT[-/AG]ACATACATGTGCCAT | 22992 |
rs748397968 | snp | C/T | 2.08592e-05 | 0.00322942 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67219388 | AAAAATATACAACAT[C/T]GAAGATCGGACACGG | 22992 |
rs748430214 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67168321 | AGGTGGAGCTTCCCC[C/T]AAACCCTCTGTGTTA | 22992 |
rs748439408 | in-del | -/GTGTGTG | | | intron-variant | KDM2A | GRCh38.p7 | 11:67172618 | TTAGCTCTTATAGTT[-/GTGTGTG]TGTGTGTGTGTGTGT | 22992 |
rs748441759 | snp | A/G | | | upstream-variant-2KB, utr-variant-3-prime | KDM2A, LOC107984341 | GRCh38.p7 | 11:67117310 | CCTTTCTATACTTCA[A/G]TTGTCTATCTTTAAA | 22992 |
rs748453107 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67227748 | GCTAATTTTTGTATT[G/T]TTAGTAGAGGTAGGG | 22992 |
rs748471702 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67242784 | CCACTGTGCCCAGCC[G/T]CAAAGTTTTGATAAT | 22992 |
rs748474142 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67190560 | AGCTCAGGAGTTTGA[A/G]ACCATCCTGGGCAAC | 22992 |
rs748485649 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67140115 | CCTATAATCCCAACA[C/T]TTTGGGAGGCTAAGG | 22992 |
rs748536017 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67133844 | GTTTACAGCCCTGCG[C/T]CACCACACCCAGGTA | 22992 |
rs748540872 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67137046 | AGTTGAGACCTAAAG[A/G]GTGACTAGGAGGTAA | 22992 |
rs748544210 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67244115 | AATCACCTCCTCGTC[C/T]CTAGTGGGAGGAGTC | 22992 |
rs748570776 | snp | C/T | 4.96816e-05 | 0.00498381 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67228067 | CGCTATCCATTCTAC[C/T]ATGAGATGTGTTGGT | 22992 |
rs748588407 | snp | C/G | 3.50349e-05 | 0.00418524 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67254974 | GATCACTCGAAAAGC[C/G]TGCGAGCACTTCATC | 22992 |
rs748632106 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67163170 | GTCTTCTAGCGCTAC[A/G]CTTTCGTATTTATGT | 22992 |
rs748643294 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67126907 | GGATAAACAATGTTT[A/G]GCTTCTCTTAAGTAA | 22992 |
rs748659600 | snp | A/T | 0.000124139 | 0.00787743 | intron-variant | KDM2A | GRCh38.p7 | 11:67181298 | TACCACTTATCTTTC[A/T]AATATTTTCCTATGG | 22992 |
rs748688351 | snp | C/T | 1.65685e-05 | 0.00287819 | intron-variant | KDM2A | GRCh38.p7 | 11:67228024 | ATCTTTTCTCTATTT[C/T]ATTCCTCTGTAGGTT | 22992 |
rs748703520 | snp | G/T | 1.72323e-05 | 0.00293528 | missense, intron-variant | KDM2A | GRCh38.p7 | 11:67250601 | GCTGGGGGGAGAGGA[G/T]GAGGAAGAGGAGGAG | 22992 |
rs748707840 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67212561 | TTCTTACCAGTTTGG[A/C]CCTAGTTTTGTTGCA | 22992 |
rs748708334 | snp | C/T | 1.68292e-05 | 0.00290075 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67254938 | CAACGTCACCTTGAT[C/T]GACCTTCGAGGATGC | 22992 |
rs748736194 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67140889 | CTGGGTTAACGTCAT[A/G]AGGTATCACCATAGA | 22992 |
rs748736435 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67198939 | ATGCACCACCATGCC[G/T]GGCTAATTTTTGTAT | 22992 |
rs748753950 | snp | C/T | 1.65921e-05 | 0.00288024 | intron-variant | KDM2A | GRCh38.p7 | 11:67121385 | CTCCCCCCACCACAC[C/T]CTCCAGTTTTAAAGT | 22992 |
rs748778202 | in-del | -/TTAC | | | intron-variant | KDM2A | GRCh38.p7 | 11:67146353 | ACACCGATTGTCTTT[-/TTAC]TTACTTTTTATAGAT | 22992 |
rs748790790 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67253380 | GAAGTTTGTTCACTT[C/T]GCTCAGATCGTTACG | 22992 |
rs748807621 | in-del | -/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67138044 | CTTGTGATTCGCCTG[-/C]CTCAGCCTCCCAAAG | 22992 |
rs748814811 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67184041 | AGGCTGAGACTGCAG[-/T]GATATGTGATCACAC | 22992 |
rs748842059 | snp | A/G | 1.6599e-05 | 0.00288084 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67180098 | GTACCATGCGACGAC[A/G]CTATGAAGATGATGG | 22992 |
rs748861069 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67148287 | TTAGCTGGGCGTGGC[A/G]GTGGACACCTGTAGT | 22992 |
rs748869918 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67171297 | AGGACAGACGAGGCC[A/G]AGTCTGAAATTAGAT | 22992 |
rs748900417 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67156545 | ACACAGTGAAACCCC[A/G]TCTCTACTAGAAAAA | 22992 |
rs748947457 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67149429 | AAGCTTAATACGTTA[C/T]TATATATAACAAGCC | 22992 |
rs748948638 | snp | C/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185950 | CATAAATTACCTACT[C/T]AGGTTTTCTGTCAAC | 22992 |
rs748983664 | snp | C/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67186182 | GATGAACTCAGAGAC[C/T]CTCACCAAGACACAT | 22992 |
rs748985237 | snp | A/G | | | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67238492 | TGCAGTGGGTCTTGA[A/G]TCTTAAGATACAGTG | 22992 |
rs749016930 | snp | A/G | 1.6566e-05 | 0.00287797 | synonymous-codon, nc-transcript-variant, intron-variant | KDM2A | GRCh38.p7 | 11:67243017 | CCCTTAGATTTTGCT[A/G]GAGGAGCTTGCCAAC | 22992 |
rs749028115 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67223456 | CACCCAGGCTGGAGT[A/G]CAGTAGCATGATCTC | 22992 |
rs749049046 | snp | C/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206829 | TCTTGTGGCCTTATG[C/T]GTTTTGTTGTAGTTG | 22992 |
rs749052730 | snp | C/T | 1.66424e-05 | 0.0028846 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67207538 | GGTGGATGTCATGGA[C/T]GTGAACACACAGAAA | 22992 |
rs749069353 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67172533 | TTTTTTATGCTATTA[C/T]AAATGGATTTTTTTT | 22992 |
rs749097197 | snp | C/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67121163 | CACTTACCTTAAATA[C/G]TCCTTTCCGTGAACA | 22992 |
rs749097255 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67136296 | ATTATCCAGTTAAGG[C/G]ACAGAGCCAGGATTC | 22992 |
rs749114662 | snp | C/G | | | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67239671 | GTGCAGTCAGCCAGA[C/G]AGCTCTGGCAGTAAC | 22992 |
rs749133651 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67220683 | AGAGTTGACAAACTT[C/T]TCCTGCAAAGGACCA | 22992 |
rs749133992 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67126554 | CTCTACTAAAAATAC[A/G]AAAATTAGCCGGATG | 22992 |
rs749140674 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67246671 | CTCCCCTACTGATCC[A/G]AATTGTGCAGCCTTT | 22992 |
rs749171554 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67143422 | CTTGGGAAGAAGCAC[A/G]TGCAGAAAAGTCCGT | 22992 |
rs749173702 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67160015 | AAAATGGTAAACTTT[A/C]TGTGTATATTACCAC | 22992 |
rs749187631 | in-del | -/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67174343 | ACATATTGTTACTGA[-/C]TCAGTGAATATTCTC | 22992 |
rs749188066 | snp | A/C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67208224 | TTTTAAAATTTTAAA[A/C/G]TTTATTATTATTAAA | 22992 |
rs749189143 | in-del | -/TA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67143003 | TAAACACTTCAGTTA[-/TA]TATATATATATCTAT | 22992 |
rs749258381 | in-del | -/GTGTGTGTGTGT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67152908 | TTACAGTGCCAGAGT[-/GTGTGTGTGTGT]GTGTGTGTGTGTGTG | 22992 |
rs749287389 | in-del | -/TGA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67230370 | GGTGGCTCATGCCTG[-/TGA]TGATCTCAGTACTTT | 22992 |
rs749298175 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67158698 | GATGGTGTCTCACTA[G/T]GTTACCCGGGCTGGT | 22992 |
rs749318173 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67179922 | TGTGGATTCTGAGAA[C/T]ATCAGCTATCTTGAG | 22992 |
rs749353463 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67129337 | CTTAGGCCTGTAATC[A/C]CAGCACTTTGGGAGA | 22992 |
rs749379681 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67234078 | ACAACAGATTTAGAT[C/T]CCAGCTCTGCAGGTG | 22992 |
rs749454804 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67167019 | GGAGACGGAGGTTGC[A/G]GTGAATTGAGATCAT | 22992 |
rs749459792 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67132578 | AGGCATGAGCCGCTG[C/T]GTCCAGCCAGTTTGT | 22992 |
rs749463357 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67147483 | GGAGGTGGAGCTTGC[A/G]GTGAGCCGAGATCGC | 22992 |
rs749496715 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67225598 | CAACATGGAGAAGGC[A/G]TGTTTCTACTAAAAA | 22992 |
rs749515965 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67181838 | ACTTACTGGTGTTTG[C/T]TTCATAGAATGCCGG | 22992 |
rs749525957 | snp | A/G | 5.0078e-05 | 0.00500365 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67252815 | CTCAGTTGGACCAAC[A/G]TCTCTAAAAAGCAAC | 22992 |
rs749574512 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67216494 | GAATGCTATATGAGA[A/G]TGGAAATCTAGAATT | 22992 |
rs749576293 | snp | C/G | 1.68049e-05 | 0.00289865 | intron-variant | KDM2A | GRCh38.p7 | 11:67245480 | GATCTGCTGGGTAAA[C/G]AATTTTGGGGAGGGG | 22992 |
rs749576639 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67170536 | CCTGCCTGAGCCTCC[-/T]CGAGTAGCTGGGACT | 22992 |
rs749577884 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67204496 | GTGTTTTCTTTTTTC[-/T]TTTTTTTTTTTTTGA | 22992 |
rs749591958 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67166013 | GCATCAATTATAAAA[A/G]GTGGTGAAGAAACTA | 22992 |
rs749609636 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67204350 | TGAGCAGTCATTCTC[C/T]GTTTTCTCCTCCACT | 22992 |
rs749612968 | snp | A/G | 1.67733e-05 | 0.00289592 | intron-variant | KDM2A | GRCh38.p7 | 11:67253405 | GTTACGGCTCTGAGT[A/G]TGCTGGGAAACAGTG | 22992 |
rs749617669 | in-del | -/CTGAAGTCTCAGCTAATGGAGTGAGTGACACAACAGA | 1.65886e-05 | 0.00287993 | intron-variant | KDM2A | GRCh38.p7 | 11:67246140 | AGCTATGAGGGGTTC[lengthTooLong]ATGGGACACTTGTGA | 22992 |
rs749617696 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255712 | CACCCCAGCCTACCC[A/G]ACTTACTTGCTAGTC | 22992 |
rs749638829 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67241058 | TCGCAGATCTTACTG[G/T]GCAGTCTGTTTTGCT | 22992 |
rs749645062 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67197206 | GAGACAGGGTATTGC[-/T]TTTGTCACCCAGGCT | 22992 |
rs749647615 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67256678 | ACTGAGAAGAGAGAC[A/G]CCAACTGCACCCTTG | 22992 |
rs749689326 | snp | C/G | | | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67119859 | ACGCCTCCGACTCCC[C/G]GTCTCCAAAGCCAGA | 22992 |
rs749704728 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67217177 | AACCCAGGAGGTGGA[C/G]GTTACGGTGAGCCAA | 22992 |
rs749706314 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67202505 | CAGCTGGGCATGGTG[A/G]CTCACGTCTGTAATC | 22992 |
rs749712054 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67232184 | TTCATTGAAGACTTA[C/T]AAATTTAGTCTTAAA | 22992 |
rs749713514 | snp | C/T | 6.62691e-05 | 0.00575588 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67246110 | TGTTCATCCTGGCTG[C/T]CTCCAGGTGAGGAGA | 22992 |
rs749739542 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67249769 | TAGTTCAAATGGTAT[A/G]TGTGGGCTTTTTCCA | 22992 |
rs749754360 | in-del | -/C | 2.58201e-05 | 0.00359296 | intron-variant | KDM2A | GRCh38.p7 | 11:67254526 | TTGATTGACCCACAT[-/C]AGCTCATTTCTTCAC | 22992 |
rs749781207 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67175797 | AAGCATATTAGAACT[A/G]AAAATGCAAGTGAGT | 22992 |
rs749797751 | snp | C/T | 1.78121e-05 | 0.00298425 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | KDM2A | GRCh38.p7 | 11:67219340 | AGTGTTTGGGGGCAA[C/T]TTTTTGCATAGCTTC | 22992 |
rs749801649 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67139899 | TTTTTTAGTAGAGTC[C/T]GGGTTTCACTGTGTT | 22992 |
rs749817847 | snp | A/G | 1.72612e-05 | 0.00293774 | intron-variant | KDM2A | GRCh38.p7 | 11:67254838 | AGGAAAGCTGTGTGT[A/G]TGTGAGCACTGTCAT | 22992 |
rs749833806 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67242666 | TCCTTTCTGCTCCCC[C/G]ACCACCACCATCCGC | 22992 |
rs749851194 | in-del | -/CA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67161462 | TAGTACAGTGTTTTG[-/CA]CAGTTTTTAACTGAC | 22992 |
rs749852754 | in-del | -/TTTTG | | | intron-variant | KDM2A | GRCh38.p7 | 11:67246941 | AGAACCGGGTTTTTG[-/TTTTG]TTTTGTTTTTGAGAC | 22992 |
rs749866802 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67245606 | TTGTACCTTTTTTCC[C/G]CAGGTTTAGATAGAA | 22992 |
rs749874759 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67189333 | AAATTAGAAAATACT[C/T]ATAGATGAATGAACA | 22992 |
rs749894685 | snp | C/T | 1.65622e-05 | 0.00287764 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67246017 | AGTCACATGTTCCCT[C/T]TGTGGAGAGGTGGAT | 22992 |
rs749911022 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67191516 | ACCAAGTGGGATTTA[C/T]TCCTGGAATAGATGA | 22992 |
rs749911600 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67141882 | TCTGTTTATGAGATC[A/T]GCTTTTTAGTTCTTT | 22992 |
rs749914761 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67140792 | TTTTGATTTATTTAT[A/G]TTAACCTTTCTGTCT | 22992 |
rs749914932 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67127522 | AAAAGATGTTATTAT[C/T]GCATGTTCAATCCTG | 22992 |
rs749954764 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67243729 | CTGGGGCAGGAGAAT[C/G]ACTTGAACCCAGGAG | 22992 |
rs750004551 | snp | A/C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67220951 | TAGGTGTTCATGCAC[A/C/G]TATGTGAAAGATGCC | 22992 |
rs750016806 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67215011 | CACCTTTTATTGGAT[G/T]AAAAAATAAAACAAA | 22992 |
rs750027796 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67164424 | ACATTTTTAGTTTCT[C/T]TGGTGGCTTGTGTAT | 22992 |
rs750072254 | snp | A/C | 3.3162e-05 | 0.00407184 | intron-variant | KDM2A | GRCh38.p7 | 11:67228003 | TCTCTTTCCTTGAAA[A/C]TCGTCATCTTTTCTC | 22992 |
rs750103534 | snp | C/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67177896 | TGTTGTGCTATGATG[C/T]CCTGATGGCAACAGT | 22992 |
rs750113380 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67192927 | AGTCAAGTAGGAGAG[C/T]GTCCTTTGTTCCATA | 22992 |
rs750138884 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67200146 | TCAAAATGTTACTGC[C/T]CACTGGCAGTGTACC | 22992 |
rs750153756 | snp | A/G | 2.44771e-05 | 0.00349828 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255059 | AAGATCAGCTAAGAC[A/G]CACCCAGCCCAGATT | 22992 |
rs750158434 | snp | A/G | 1.65644e-05 | 0.00287783 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67228157 | CAGAAAGAGTCCCTC[A/G]GCATGGGTAAGTATT | 22992 |
rs750210169 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67165498 | ATTTCATAAATCTTA[A/T]GTTTGACAGTTTGAA | 22992 |
rs750238183 | snp | A/C/G | 0.000114715 | 0.00757269 | intron-variant | KDM2A | GRCh38.p7 | 11:67254484 | TCCCTGGAACTTGAT[A/C/G]AGTAAACCAGAATGA | 22992 |
rs750239468 | snp | C/T | 1.76452e-05 | 0.00297024 | synonymous-codon, intron-variant | KDM2A | GRCh38.p7 | 11:67250697 | GGCTCAGGATGGAGA[C/T]GAAAGCTGGATGCAG | 22992 |
rs750241715 | snp | C/T | 0.00016657 | 0.00912453 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255617 | CAAACCTCACGTCCT[C/T]AACTGTGCTCTCCCT | 22992 |
rs750252227 | snp | A/G | 3.49119e-05 | 0.00417789 | intron-variant | KDM2A | GRCh38.p7 | 11:67181272 | TATGGTCCTTTTATC[A/G]TTTTTAATTATACCA | 22992 |
rs750281542 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67223454 | GTCACCCAGGCTGGA[A/G]TGCAGTAGCATGATC | 22992 |
rs750292603 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67158578 | CATTTGGTGTTGTAT[G/T]TTCAATTTTGACCGT | 22992 |
rs750294786 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67191260 | TCGATCTCCTGACCT[C/T]GTGATCTGCTCGCCT | 22992 |
rs750342943 | snp | C/T | 1.6601e-05 | 0.00288101 | intron-variant | KDM2A | GRCh38.p7 | 11:67242994 | ATTTTTCCTTCTTTT[C/T]CCTCCTACCCTTAGA | 22992 |
rs750347782 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67135944 | TAGCTCATCCTATCA[C/T]ATACTTTCATTGCAT | 22992 |
rs750351832 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67152397 | TGAGGTTGGAGGGTC[A/G]TTTGAGACCAGCCTG | 22992 |
rs750371031 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67186724 | ACTGAAACTTTGAGT[A/G]TAGCCCCACATTTTA | 22992 |
rs750377296 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67201895 | AGGAATTCGAGGTTG[C/T]AATGAGCTCTGATCT | 22992 |
rs750384287 | snp | C/T | 1.6646e-05 | 0.00288491 | intron-variant | KDM2A | GRCh38.p7 | 11:67243114 | AACTATTTTCCTTGA[C/T]CTTTAGGCTGCTTAA | 22992 |
rs750401069 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67150899 | TAGCATTCACCTCTT[C/T]TTTCATCCTAGTCTT | 22992 |
rs750420506 | snp | A/G | | | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67239627 | TGGGCGACCCCCTCT[A/G]CTTGCTGAGAGGGGA | 22992 |
rs750422978 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67123885 | TTTCACCTTGTTGGC[C/T]AGGCTGGTCTCGAAC | 22992 |
rs750426210 | in-del | -/T | 1.65693e-05 | 0.00287826 | intron-variant | KDM2A | GRCh38.p7 | 11:67215842 | CACTAATGCTGCTGC[-/T]TTTTTTGGGTCAGGT | 22992 |
rs750431980 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255308 | ACAGGCTGTGCTGTC[C/G]AGGCGCCTGCTCGCT | 22992 |
rs750460384 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67232683 | AATCCAGACTTGAGC[-/T]TTTTTTTTTTTTTTT | 22992 |
rs750462694 | snp | C/T | 4.96816e-05 | 0.00498381 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67254337 | CTCAGTCACTGCAGC[C/T]ACCTTACAGATCAGT | 22992 |
rs750487972 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67128103 | GCATCAGCCTCCCCA[A/G]GTGATCCTCTTACCT | 22992 |
rs750497992 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67240589 | ATCCTTTCCCTCTCT[C/G]CCCAGGCACCTTCTG | 22992 |
rs750506870 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67137569 | TAAAGGAGGTAAATA[G/T]AAGTATGACTCCCAA | 22992 |
rs750523387 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67122488 | TGTGCCACCACGTCC[A/G]GCTAATTTTTGTATT | 22992 |
rs750550183 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67223355 | ACTCAAAATTTTAAT[A/G]CCTGTATTTCATATT | 22992 |
rs750571134 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67173401 | TGTGGGGATTACATG[C/T]GTGAGCCACCGTTCT | 22992 |
rs750579484 | snp | C/G | 1.70781e-05 | 0.00292212 | intron-variant | KDM2A | GRCh38.p7 | 11:67254460 | AGCGGTGCCCCCTGC[C/G]TCCAGCCCTCCCTGG | 22992 |
rs750589656 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67241843 | GGAGGCCGAGGCAAG[C/T]GGATCACCTGAGGTC | 22992 |
rs750611586 | snp | A/G | 1.67829e-05 | 0.00289675 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67121268 | AGGAGGAAGAGGAAG[A/G]CAGCCCTGGAGTGGT | 22992 |
rs750625234 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67211092 | AACATAGCTACAATC[A/T]TGTTATTTTTGTTGT | 22992 |
rs750650123 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67248384 | AGGTAAAGGAACCTT[A/G]TCAGATTTGCACTGT | 22992 |
rs750660679 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67159829 | CAGCAGGGAACATTT[A/G]CAGTTTAGGATATGT | 22992 |
rs750670089 | in-del | -/TAATAAATTTTAAAATTTTAAAATT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67208202 | CATTTTCCGAAATCA[-/TAATAAATTTTAAAATTTTAAAATT]TATTATTATTAAAAA | 22992 |
rs750670986 | in-del | -/AAA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67189300 | AACAATCAGTGAATC[-/AAA]GAAGAAATCACATGG | 22992 |
rs750671474 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67160891 | GGCAGGAGAATTGCT[G/T]GAGCCCAGGAGTTCA | 22992 |
rs750681326 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67247037 | ATGTTATAAATTATT[A/T]TATATATATATATAT | 22992 |
rs750690100 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67137057 | AAAGGGTGACTAGGA[A/G]GTAACCAGGCAAAGA | 22992 |
rs750714887 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67209006 | GGTGGCACGATCTCG[A/G]TTCACTGCAACCTCT | 22992 |
rs750719229 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67203629 | TATGGTGGCATGCAC[-/T]TGTAGTCCCAGCTAC | 22992 |
rs750746262 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67147192 | CGCCTGTTTGTATTT[C/T]ATCCAGGCTTGGCCA | 22992 |
rs750749650 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67132399 | AGCGATTCTCCTGCC[C/T]CAGCCTCCCAAGTAG | 22992 |
rs750761051 | snp | G/T | 1.66076e-05 | 0.00288158 | synonymous-codon, intron-variant | KDM2A | GRCh38.p7 | 11:67250508 | CATCACGGCCTCCTC[G/T]GCCAACCTTCGCCAT | 22992 |
rs750784145 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67195997 | ATTTCTTCAAACTTA[C/T]CTCAGAACCACAAGA | 22992 |
rs750785218 | snp | A/G | 6.62548e-05 | 0.00575526 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67231866 | AGCTTGAAGGCCTTC[A/G]CTGCCTTGTAGATAA | 22992 |
rs750795791 | in-del | -/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67225141 | CGGCTGCAGCATTTA[-/C]CCCAAGATAACTTTG | 22992 |
rs750821669 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67249471 | GTTCCTAGTGGAACA[C/T]GTTTACTGGGCTTTG | 22992 |
rs750828412 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67167678 | TGCTAAATTCTGTAG[A/G]CACCTTCTATTTATG | 22992 |
rs750849359 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67237944 | AAAATTTATATCCTG[-/T]TATAGGATATATTTA | 22992 |
rs750864807 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67204200 | ACCATTACGTTTTTT[C/T]CTTTTTGCATAGAAC | 22992 |
rs750873285 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67133238 | CCAGGTAGCTGGGAT[C/T]ACAGGCGTGCGCCAC | 22992 |
rs750886965 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67150911 | CTTCTTTCATCCTAG[A/T]CTTCAGTCTAAACCT | 22992 |
rs750891432 | snp | A/C/T | 1.83518e-05 | 0.00302912 | intron-variant | KDM2A | GRCh38.p7 | 11:67252904 | GGGGCCCAGAAGAAG[A/C/T]GGGCAAGAAAAGTTG | 22992 |
rs750906484 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67142902 | AAGCTTCAACAATTA[-/T]CAAAACTTGGAAATC | 22992 |
rs750931088 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67218123 | TTTTCAGGTATACAC[A/G]TTTGGGCTCTGCATT | 22992 |
rs750948728 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67181518 | ATAATTTCCCACTTT[A/G]TTTTAAAAGTATATG | 22992 |
rs751006196 | in-del | -/TCTT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67169758 | CTCTCTCTCTCTCTC[-/TCTT]TTTTTTTTTTTTTTG | 22992 |
rs751034713 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67205159 | CTCTGCATTTTTGCT[A/G]GCACTCATTATTTTC | 22992 |
rs751060906 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67257782 | AAGTTTAAATTAAAT[A/G]TAAGCATTAAGGGGA | 22992 |
rs751060922 | in-del | -/A | 1.65611e-05 | 0.00287755 | intron-variant | KDM2A | GRCh38.p7 | 11:67252626 | TTTCCCAGAAGCCAT[-/A]AGCAGCCTGTGATGG | 22992 |
rs751076811 | snp | G/T | 1.7312e-05 | 0.00294205 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67207482 | ATTAGTGGCTCGATA[G/T]AGATGATCGATGCAT | 22992 |
rs751080254 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67234599 | TTGGGCTGAGCCCAG[G/T]GGCTCACACCTCTTG | 22992 |
rs751080966 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67256516 | TGATAGCACAACCTC[C/T]TCCCCCCACCCCGCC | 22992 |
rs751097056 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67166897 | GCCTGGCCAACGTGG[C/T]GAGACCTCGTCTCTA | 22992 |
rs751103780 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67121795 | TGAGCGGGGAGAACT[A/G]TGGATTATTTTCTTT | 22992 |
rs751139810 | snp | C/T | 1.75274e-05 | 0.0029603 | intron-variant | KDM2A | GRCh38.p7 | 11:67252876 | AGTGAGCAGCCCTGC[C/T]GCTGTCTTTCCAGGG | 22992 |
rs751159831 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67191442 | CAATGATGTAAAACT[C/T]CTCAACAAAATACTT | 22992 |
rs751189132 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67169020 | GAGTGTAGTGGTGTG[A/T]TCTCAGCTCACTGCA | 22992 |
rs751223546 | snp | C/G | 1.66095e-05 | 0.00288175 | intron-variant | KDM2A | GRCh38.p7 | 11:67245965 | CAGTTCTCTTGGATT[C/G]TATCTTTGTCCTCTT | 22992 |
rs751227489 | snp | A/G | 3.25061e-05 | 0.00403137 | intron-variant | KDM2A | GRCh38.p7 | 11:67219250 | GACTTACTGTAATGT[A/G]TGTTTTCAGCCACTG | 22992 |
rs751228912 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67189975 | AAAGATTAGAGATAA[A/G]TGAAATAAAGAATAG | 22992 |
rs751246411 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67140613 | AAAAAATTAGCCAGG[C/T]GTTGTGGCAGGCGCC | 22992 |
rs751259146 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67243537 | AGAAGAAAGGGGCCG[C/G]GCATGGTGGCTCACA | 22992 |
rs751299318 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67155567 | CCTCAGCCTCTCAGG[C/T]TGCTGGGATTACAGG | 22992 |
rs751308530 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67230496 | CTGAGTGTTGGGGCA[C/T]ATGCCTCTGGTCCCA | 22992 |
rs751327791 | in-del | -/AA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67125942 | GCAAGGCTTCACCTC[-/AA]AAAAAAAAAAAAAAA | 22992 |
rs751408295 | snp | A/G | 1.66832e-05 | 0.00288814 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67254913 | CCCTGATCTACCTAC[A/G]GCGCATTGCCAACGT | 22992 |
rs751496172 | snp | G/T | 2.00813e-05 | 0.00316864 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255022 | CAGCCTCTACTGCCT[G/T]TCTGACGAGAAGCTG | 22992 |
rs751520227 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67199903 | AAGGGACAAGTTGAC[C/T]CTCTTGTTAGGGGCT | 22992 |
rs751525867 | snp | A/G | | | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67239320 | GTGGAACTGCTGCAG[A/G]ATTGCTGCGCAGACA | 22992 |
rs751547184 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67164245 | AATCCATTTGTTCTT[C/T]TGATTATGTAGTTTT | 22992 |
rs751556166 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67135555 | ATCCTGGATCACAGA[C/T]GTTAGCAACTTTTTT | 22992 |
rs751593636 | snp | A/G | 1.65616e-05 | 0.00287759 | missense, nc-transcript-variant, utr-variant-5-prime | KDM2A | GRCh38.p7 | 11:67215876 | GTCTAATGAGTGTTC[A/G]AGGCTGCTATACTGA | 22992 |
rs751605889 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67150534 | GGCCAATTAGGGAAG[A/G]AGATTGATTTTGAAA | 22992 |
rs751614732 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67198047 | CTATTAAGATTGAAA[A/G]TATATTTACTATCTT | 22992 |
rs751642792 | snp | C/T | 1.90536e-05 | 0.00308649 | intron-variant | KDM2A | GRCh38.p7 | 11:67254173 | AGAGAATTGAGAGTT[C/T]TGATCTAGGCTCTTC | 22992 |
rs751665022 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67158092 | AATCTACTGTGCACC[A/G]CTTATTCATCCCCTT | 22992 |
rs751674205 | in-del | -/AAAAT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67196690 | CAAAATCATGGAGAC[-/AAAAT]AGAATAGTGGTTACT | 22992 |
rs751693168 | snp | A/G | | | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67238136 | GTATTATGTAATGTC[A/G]TGGTCTTAGTAATTC | 22992 |
rs751745156 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67171969 | AGTTTTGAAATTACT[A/G]TAGTTTTATAGTGAG | 22992 |
rs751752033 | snp | C/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67207453 | TAAAAAATATTCTTA[C/T]TATATTTAAGGATAT | 22992 |
rs751785296 | snp | A/T | 1.8636e-05 | 0.00305249 | intron-variant | KDM2A | GRCh38.p7 | 11:67217712 | GGCTGTTAACAGACT[A/T]AAGTTTTTTAACTCA | 22992 |
rs751803631 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67173293 | ATGCGTGGCTAATTT[C/T]GTATTTTTAGTAGAG | 22992 |
rs751807733 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67237737 | AGGATCACTTAAGGC[C/G]AGGAGTTCAAGACCA | 22992 |
rs751836720 | in-del | -/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67247632 | GTTTCACCATGTTGG[-/C]CAGGTTGGTCTTGAA | 22992 |
rs751872758 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67208891 | CAAGATCAGCCTGGG[A/G]AATGTCACGAGACCC | 22992 |
rs751885015 | in-del | -/TT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67182532 | AAATTGAATAAGTCT[-/TT]TTTTTTTTTTTTTTT | 22992 |
rs751891592 | snp | G/T | 1.67019e-05 | 0.00288975 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67250288 | ACCACAGTGCCAGCC[G/T]CGATGAGCGCTTCAA | 22992 |
rs751900605 | snp | C/T | 1.6628e-05 | 0.00288335 | missense, splice-donor-variant | KDM2A | GRCh38.p7 | 11:67250348 | CAGAGCGCACCATGG[C/T]ACGGGAAAAGGAGAA | 22992 |
rs751906042 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67193370 | CCTGTAAGGATAATC[A/G]TGTTCTCAGAAATGT | 22992 |
rs751906788 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67208032 | CAAGACCCTGTCTCA[A/G]AAATTTAAAATAAAA | 22992 |
rs751975510 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67159690 | AGAAATATTTGACTC[A/C]ATATTTGTCAGGCAT | 22992 |
rs751978635 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67216232 | AAATGAAGCCAAAGA[A/G]GTGATTTTAGAAGGA | 22992 |
rs751993163 | snp | A/C | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67178568 | TTCTCTAGCCCCTGG[A/C]AACTATGAATCTAGT | 22992 |
rs752026594 | in-del | -/TTAT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67223393 | TTTTTTCTTTCTTAT[-/TTAT]TTATTTATTTATTTA | 22992 |
rs752036560 | snp | A/G | 3.34958e-05 | 0.00409228 | intron-variant | KDM2A | GRCh38.p7 | 11:67181805 | ACATTTACTAGAGCA[A/G]TTGTGTTTTCCATAT | 22992 |
rs752036883 | snp | C/G | 1.65946e-05 | 0.00288046 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67231765 | GGACTCATCTTCTGA[C/G]TGTAGCCGGGGCTCC | 22992 |
rs752046811 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67145614 | CCTAACGTTATACTA[C/T]TAAGCAGTAGAACAA | 22992 |
rs752064436 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67232971 | TGCCTCAGCCTCCCA[A/G]AGTGCTGGGATTACG | 22992 |
rs752108775 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67203004 | TGTCCGTCCGCCGCC[-/A]AAAAAAAAAAAAAAG | 22992 |
rs752115636 | snp | A/C | | | upstream-variant-2KB, utr-variant-3-prime | KDM2A, LOC107984341 | GRCh38.p7 | 11:67117540 | TTGTCTCGCTAACGT[A/C]CTCCTGAAAGAGTTG | 22992 |
rs752195376 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67216812 | ATAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 22992 |
rs752204481 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67132154 | TACTACTATAAGGCC[C/T]ATTCTGTGGATCTCT | 22992 |
rs752242185 | snp | C/G | 1.66181e-05 | 0.00288249 | intron-variant | KDM2A | GRCh38.p7 | 11:67181910 | AAGTGTCGAGCTTTT[C/G]GCCTCTGTCTTTAAG | 22992 |
rs752245877 | in-del | -/A | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185852 | ATGTGATGATGCAGC[-/A]AAAAAGGCCCTCACC | 22992 |
rs752270902 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67205044 | TTGCTGAGTCACATG[A/G]TCATTCTGTGTTTAG | 22992 |
rs752283155 | snp | A/C | 1.66707e-05 | 0.00288705 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67252707 | AGGTGCTGCGACAAG[A/C]GACTTTGGACAAAAA | 22992 |
rs752300929 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67226717 | ACAGAGCAAGACTCC[A/G]TCTCAAAAAACAAAC | 22992 |
rs752327111 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67188723 | TTGAGCCTGGCAGGT[C/T]AAAGCTGCAGTGACC | 22992 |
rs752328206 | in-del | -/GAGGAGGAGGAG | 3.73552e-05 | 0.0043216 | cds-indel, intron-variant | KDM2A | GRCh38.p7 | 11:67250608 | GGAGAGGAGGAGGAA[-/GAGGAGGAGGAG]GAGGAGGAAGATGAC | 22992 |
rs752349127 | in-del | -/TTAAGCCTT | 3.33784e-05 | 0.0040851 | intron-variant | KDM2A | GRCh38.p7 | 11:67243126 | TGATCTTTAGGCTGC[-/TTAAGCCTT]TTGTTAGTTGATCAT | 22992 |
rs752354083 | in-del | -/TG | 0.00746397 | 0.0606323 | intron-variant | KDM2A | GRCh38.p7 | 11:67196339 | GAGATGAGGTCTCAC[-/TG]TGTTGCCCAAGCTGG | 22992 |
rs752380945 | snp | A/G | 6.62811e-05 | 0.0057564 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67245368 | CTGTGTGCAAGGAGA[A/G]TGTGGTGTTTGCCAC | 22992 |
rs752391526 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67125427 | CTCAAACGATCTGCC[C/T]GCCTTGGCCTCCCAA | 22992 |
rs752399342 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67175445 | TCCGAAAAAAACCAG[C/G]ACACACACACGTAAT | 22992 |
rs752415018 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67204080 | TGCTGAGATTACAGG[C/T]GTGAGTCACCACACC | 22992 |
rs752444438 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67139357 | TCAAATGATTCTCCT[G/T]CCTGAGCCTCCCAAG | 22992 |
rs752445776 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67167391 | TGATGGGAGAGATCT[A/C]GCACTTTTAACTCAT | 22992 |
rs752449240 | snp | A/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67121169 | CCTTAAATACTCCTT[A/T]CCGTGAACAGAAAGC | 22992 |
rs752453568 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67189876 | TCTTTAACAAAAGAA[A/G]AGAAACTTAAAATCA | 22992 |
rs752466840 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67242042 | TAGCGCCACTGCACT[A/C]CAGCCTGAGCAACAG | 22992 |
rs752480907 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67227188 | AATCTGGTTTGTGGA[C/G]ATACCATTTTGGCAG | 22992 |
rs752486965 | snp | C/G | 0.000275819 | 0.0117402 | intron-variant | KDM2A | GRCh38.p7 | 11:67252869 | CCAGGTAAGTGAGCA[C/G]CCCTGCCGCTGTCTT | 22992 |
rs752518269 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67134720 | ACGTTGACTAGGCTG[G/T]TCTCGAACTTCTGAC | 22992 |
rs752523087 | snp | C/T | 1.75121e-05 | 0.00295901 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | KDM2A | GRCh38.p7 | 11:67217775 | CAACCTGGAGCTGTA[C/T]GAGAATTGGCTGCTG | 22992 |
rs752530962 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67133074 | TTTAGTATCAAGTCT[C/T]TTACCAATTGTGCTT | 22992 |
rs752563773 | snp | C/T | 3.32762e-05 | 0.00407885 | intron-variant | KDM2A | GRCh38.p7 | 11:67245955 | AGATCTGAGTCAGTT[C/T]TCTTGGATTCTATCT | 22992 |
rs752578593 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67256203 | GAGTGTATTCTGCGC[G/T]TGTGTGTGGAGGGAG | 22992 |
rs752592217 | snp | G/T | | | splice-acceptor-variant | KDM2A | GRCh38.p7 | 11:67248280 | CTCTGTCTTCCTATA[G/T]ATGGACGGAGAGGGG | 22992 |
rs752633474 | snp | A/G | | | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67252730 | GACAAAAATTGACTT[A/G]AGTAGGTGTAAGGCC | 22992 |
rs752653642 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67127229 | AGCATGTAGCTGGGA[C/G]TACAGGCATGCATGT | 22992 |
rs752658691 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67213005 | TGTTCTGGGACCGGC[A/G]GATGCTTGGTTAAAA | 22992 |
rs752658983 | snp | C/G | 5.16836e-05 | 0.00508322 | synonymous-codon, intron-variant | KDM2A | GRCh38.p7 | 11:67250658 | GGAGGGGGGTGCAGC[C/G]AGGCTGAATGGCCGG | 22992 |
rs752677551 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67197676 | CTTTCTGTGATAGGA[A/T]GTATTTGGTTGAGAA | 22992 |
rs752709262 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67236683 | TTTATGGAAACCTAT[C/T]TTCTCCTCTATAAAA | 22992 |
rs752739000 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67163935 | TCATTTAATCCTCAT[A/G]CAACCCTGTGGAATG | 22992 |
rs752747030 | snp | A/G | 1.67438e-05 | 0.00289338 | intron-variant | KDM2A | GRCh38.p7 | 11:67242973 | CTCTTTGTTCACCCT[A/G]CCCTGATTTTTCCTT | 22992 |
rs752748576 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67211977 | ATATGCATTTATATA[A/C]ACTATAGTATGAGCA | 22992 |
rs752750324 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67228274 | TTTTTTAATTCATCT[A/T]CTTGGAAGTACCAAA | 22992 |
rs752761808 | snp | C/T | 3.6501e-05 | 0.00427191 | intron-variant | KDM2A | GRCh38.p7 | 11:67232000 | CAGCTACTGATCCAG[C/T]TATGGCAGTCAGCTT | 22992 |
rs752771419 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67182618 | GCTCACTGCAACCTC[C/T]GCCTGCTGCATTCGA | 22992 |
rs752786374 | in-del | -/GTGG/GTGTGG | | | intron-variant | KDM2A | GRCh38.p7 | 11:67201221 | TATATATATATATGT[-/GTGG/GTGTGG]GTGTGTGTGTGTGTA | 22992 |
rs752799295 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67251103 | AACTTGAGAGTCTTG[C/G]GGGCTGAAAATTTCC | 22992 |
rs752804371 | in-del | -/ATAA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67196630 | CCCAGCCACAAAAAT[-/ATAA]ATAAATACTGTGTAA | 22992 |
rs752821172 | in-del | -/AAAAGG | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185169 | GAGACAGAAAACCTT[-/AAAAGG]AAATTCTGGAGCTGA | 22992 |
rs752842716 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67147152 | AACACTGTTGTTGAC[A/G]GTTTGGTGTAAGAGA | 22992 |
rs752846014 | in-del | -/TAC | | | intron-variant | KDM2A | GRCh38.p7 | 11:67132136 | ACAGCATAAGCTTTA[-/TAC]TACTACTATAAGGCC | 22992 |
rs752902240 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67148917 | CTGGGGTAGGGGCTG[A/G]TGGCGCATAGCTCAG | 22992 |
rs752912077 | in-del | -/TTTT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67155015 | ACTTGTTTTTAGTTC[-/TTTT]GTTTTTTGTTTGTTT | 22992 |
rs752941431 | snp | A/G | 8.28741e-05 | 0.00643663 | synonymous-codon, nc-transcript-variant, intron-variant | KDM2A | GRCh38.p7 | 11:67243086 | ACAGTGGCCAAAAAG[A/G]GATAAGGTAAGAAAC | 22992 |
rs752944749 | snp | C/T | 2.2639e-05 | 0.00336437 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | KDM2A | GRCh38.p7 | 11:67207682 | TATGGTGCAGAGGCC[C/T]TCCACGGTTAGTGTA | 22992 |
rs752970299 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67199589 | GCCACAGTAAAGCCC[A/T]GATTCTCTTTAATTC | 22992 |
rs753029260 | snp | C/T | 1.66225e-05 | 0.00288287 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67254240 | CCGGAACATGACCGA[C/T]TTCCGGCTGGCAGGC | 22992 |
rs753030722 | snp | C/G | 1.65699e-05 | 0.00287831 | intron-variant | KDM2A | GRCh38.p7 | 11:67215822 | TGTACTTTTTTCCAT[C/G]AGTACACTAATGCTG | 22992 |
rs753043635 | snp | C/G | 7.73395e-05 | 0.00621802 | intron-variant | KDM2A | GRCh38.p7 | 11:67254166 | CTGGATTAGAGAATT[C/G]AGAGTTTTGATCTAG | 22992 |
rs753048668 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67203475 | TTAATTATTAATAAT[A/T]ATTAATATATATTAA | 22992 |
rs753056067 | snp | C/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206513 | AGGCCAAGACAGGCG[C/G]ATTGCCTGAGCTCAG | 22992 |
rs753059015 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67121857 | AAGGGTTGTTGGGAT[G/T]GATTGAAGACAAGTA | 22992 |
rs753079124 | snp | C/T | 0.000323561 | 0.0127152 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67250166 | CTGCGATGAGCCTCT[C/T]ACGCCCCCGCCTCAT | 22992 |
rs753085500 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67156541 | GCTAACACAGTGAAA[C/T]CCCGTCTCTACTAGA | 22992 |
rs753147591 | snp | C/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67207245 | AGCATTTAGAATTGT[C/T]AGGATTAAATGAGAC | 22992 |
rs753167233 | snp | A/G | 3.34879e-05 | 0.0040918 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67250269 | GGGGCTGGCCCCAGC[A/G]ACCACCACAGTGCCA | 22992 |
rs753196445 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67245757 | CCGGGGAGGCCAAGT[A/G]TAGGCCAACTGAAAA | 22992 |
rs753239274 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67193150 | TCTTGCCACCACACC[C/T]GGCTCATTTTTGTAT | 22992 |
rs753248647 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67157864 | CAGCTACTCCAGGTG[A/G]GGCTCACTTGAGCTC | 22992 |
rs753255686 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67191839 | AGTCCTAACAGAGCA[A/G]TTAGGCAAAAAAAGG | 22992 |
rs753283444 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67215245 | TATAGTTTTTTGTTA[C/T]GTATTTTAAGAAATT | 22992 |
rs753333984 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67232828 | TTCTCGTGCCTCAGC[C/T]TCCTGAGTAGCTGAG | 22992 |
rs753360367 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67166602 | GGTGGCATAAGACCT[C/G]TAGTCCCAGTAACTT | 22992 |
rs753374116 | in-del | -/AG | 9.23591e-05 | 0.00679493 | intron-variant | KDM2A | GRCh38.p7 | 11:67250813 | GGTGAGCAGGGATTC[-/AG]GGGGTCAGGAATTAG | 22992 |
rs753397630 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67143777 | AGCTGGGATTACAGG[C/T]GTGTGCCACCATGCC | 22992 |
rs753411833 | in-del | -/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67139914 | GGGTTTCACTGTGTT[-/G]GCACTGGCTGGTCTC | 22992 |
rs753413193 | snp | G/T | 2.30731e-05 | 0.00339647 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67231616 | GATGAGGAAGCAGTG[G/T]ATCGAGAACCCCGAC | 22992 |
rs753423848 | snp | C/T | 3.3134e-05 | 0.00407012 | intron-variant | KDM2A | GRCh38.p7 | 11:67228180 | TAAGTATTCTGCCTA[C/T]AGGAGCTTTGAAGAC | 22992 |
rs753423863 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67247779 | TTGGTGAAGATGTAA[A/G]TGGTGCATATTACAT | 22992 |
rs753428105 | snp | A/C | 2.57132e-05 | 0.00358552 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255067 | CTAAGACACACCCAG[A/C]CCAGATTCAACAGGA | 22992 |
rs753429292 | in-del | -/CT | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67258068 | AAAAAAATAAAAAGG[-/CT]TTAAAAACAAAAACT | 22992 |
rs753434798 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67179431 | GGCATGTGCCACTAC[A/G]CCCAGCTTATTTTGT | 22992 |
rs753463672 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67202077 | GACTTTGAGGGGTTC[A/G]AGACTTCAGTGGAGG | 22992 |
rs753509256 | snp | C/T | 1.6896e-05 | 0.0029065 | intron-variant | KDM2A | GRCh38.p7 | 11:67252590 | ACACTTGTAGAAGAA[C/T]GAGCCTCCAGGTACT | 22992 |
rs753518729 | snp | C/T | 0.000101831 | 0.00713479 | intron-variant | KDM2A | GRCh38.p7 | 11:67181285 | TCGTTTTTAATTATA[C/T]CACTTATCTTTCTAA | 22992 |
rs753526413 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67151060 | GGTGGATAGTAGAAG[C/T]AGGGGTTCAGTTTAG | 22992 |
rs753535978 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67186789 | AATAATTAGTAGAAC[A/G]GGGTATAGTGGTATA | 22992 |
rs753561636 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67181069 | CATATTATTTAAGCT[C/G]TAAATTTCCTGTGGA | 22992 |
rs753564229 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67254627 | CGGTTGCCTGTCTGC[A/G]CAGCCAACATCCAGC | 22992 |
rs753593892 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67152696 | TTTGAGCTCCACTGG[C/G]CTGGAACAACCCATA | 22992 |
rs753683101 | in-del | -/CTC | 4.77441e-05 | 0.00488567 | intron-variant | KDM2A | GRCh38.p7 | 11:67219281 | CCCTCTGTTCCCCTT[-/CTC]CTAGGCTGGATTCAT | 22992 |
rs753687697 | snp | A/C/G | 6.76184e-05 | 0.00581425 | intron-variant | KDM2A | GRCh38.p7 | 11:67252687 | GTTCTCTTCCCTTCT[A/C/G]TCACAGGTGCTGCGA | 22992 |
rs753689622 | in-del | -/TA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67188147 | CTGATCACACCACTG[-/TA]TAGTCCAGCCTGGGT | 22992 |
rs753716609 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67192110 | AGAAATTAACCTTTT[A/G]CCATATTTACTTCAT | 22992 |
rs753718796 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67131012 | CTCTCATACCATCCA[A/G]CGTCTCTTGTGTACT | 22992 |
rs753747523 | snp | C/T | 1.65682e-05 | 0.00287817 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67245356 | AAAATGCAAAGCCTG[C/T]GTGCAAGGAGAGTGT | 22992 |
rs753775499 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67209306 | AGACAGGTGGTTAGA[A/G]TTTAGCCTTCTTATT | 22992 |
rs753807204 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67175345 | AAGGTTGGAGGATCA[C/T]TTGAGCCCAGGAGGT | 22992 |
rs753807859 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67211333 | AAATATAGAAAATAA[A/G]CCAGGTGCGGTAGCT | 22992 |
rs753835308 | snp | A/G | 1.75038e-05 | 0.00295831 | synonymous-codon, nc-transcript-variant, splice-acceptor-variant | KDM2A | GRCh38.p7 | 11:67217754 | GCTCATCCCCCCTAC[A/G]GCCCACAACCTGGAG | 22992 |
rs753886232 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67242005 | ACACGGGAGGCGAGG[C/T]GGAGGTTGCAGTGAG | 22992 |
rs753904590 | snp | A/C/T | 3.31533e-05 | 0.00407134 | synonymous-codon, intron-variant | KDM2A | GRCh38.p7 | 11:67250412 | TGAGAAAGCCAAGAT[A/C/T]CGGGGATCGTACCTC | 22992 |
rs753909975 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67176286 | GCCCTTTCACAGACT[G/T]CTACTCCCTAAGAGA | 22992 |
rs753917210 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67125354 | CCTGGTTAATTTTTG[G/T]ATTTTTTGTAGAGGT | 22992 |
rs753928897 | in-del | -/GTGTGTGTG | | | intron-variant | KDM2A | GRCh38.p7 | 11:67152942 | TGTGTGTGTGTGTGT[-/GTGTGTGTG]TGTTTTCAGGAATTC | 22992 |
rs753944944 | in-del | -/TATT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67133096 | TTGTGCTTTTATTCG[-/TATT]TATTTATTTATTTAT | 22992 |
rs753950426 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67132638 | GGCATTTTGGGAGTA[A/G]TGTCTCCAGTTTCAG | 22992 |
rs753955976 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67179944 | TATCTTGAGAGAAAG[A/G]AAAGATCCATAAGGC | 22992 |
rs753997374 | snp | A/C | 3.33467e-05 | 0.00408316 | synonymous-codon, intron-variant | KDM2A | GRCh38.p7 | 11:67250526 | CAACCTTCGCCATTC[A/C]CCCCGTGTGCTAGTG | 22992 |
rs754011048 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67196088 | TAAGCTGAGTCACAC[C/G]AACATAATTGTCGGT | 22992 |
rs754044847 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67183254 | GACAGAACACTCAGG[A/G]GACCTCAGAAAACCT | 22992 |
rs754046694 | snp | A/G | 3.3168e-05 | 0.00407221 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67181852 | GTTTCATAGAATGCC[A/G]GATCCAGACTTCACT | 22992 |
rs754097270 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67237643 | GGTCCAGGCTTACAG[A/T]TTTTTTTTTGTAAAG | 22992 |
rs754123806 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67122100 | TAGTAGTCTCACAGT[A/G]TTAATAAAAATCTGA | 22992 |
rs754149469 | snp | G/T | 1.71146e-05 | 0.00292524 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67207506 | GATGCATCTTTTATG[G/T]CAGGGAGTCGTCGCA | 22992 |
rs754156911 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67162138 | ATGATGGATAAATTA[G/T]AGTTTATTAAATCAT | 22992 |
rs754156938 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67145946 | CAACATGTTTCTCTG[C/T]TTCTGGTATATAAAA | 22992 |
rs754160351 | snp | A/C | 1.75542e-05 | 0.00296256 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | KDM2A | GRCh38.p7 | 11:67207631 | GAAACTCTATAATGT[A/C]ATCAGCCTCGAGTTT | 22992 |
rs754175045 | snp | A/C | 0.000202327 | 0.010056 | intron-variant | KDM2A | GRCh38.p7 | 11:67240417 | TTGGGGTGCGTGTAA[A/C]TATAGGGACTTTTGT | 22992 |
rs754182468 | snp | A/C | | | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67119858 | GACGCCTCCGACTCC[A/C]GGTCTCCAAAGCCAG | 22992 |
rs754234839 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67168206 | GAAGAGATCACTGCT[A/G]TAGAGGAGCAACACA | 22992 |
rs754237245 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67184352 | TACAAAAATTAGGCC[A/G]GGTGCGGTGGTTGAC | 22992 |
rs754247487 | snp | C/T | 1.65614e-05 | 0.00287757 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67253524 | ACCTCCAGCTGCCCC[C/T]TTCTCAGGACCCTTG | 22992 |
rs754276938 | snp | A/C | | | intron-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67120459 | TTAGAAAAAAGAAAA[A/C]CCTTTCTTGGTATTA | 22992 |
rs754331453 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67200562 | TGTTGCCCAAGTTGG[A/G]GTGCAATGGTACAAT | 22992 |
rs754336823 | in-del | -/CT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67220470 | ACACTGATGACTATA[-/CT]CTCAAAGCATCTTAC | 22992 |
rs754337092 | snp | A/G | 3.8909e-05 | 0.00441055 | intron-variant | KDM2A | GRCh38.p7 | 11:67254159 | CTTGAAGCTGGATTA[A/G]AGAATTGAGAGTTTT | 22992 |
rs754342356 | snp | C/G | | | downstream-variant-500B | KDM2A | GRCh38.p7 | 11:67258430 | CTAGGATTACAGGCA[C/G]TTACCATCATGTCCA | 22992 |
rs754361972 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67170557 | AGCTGGGACTGCAGG[C/T]ACCTGCTACCACACC | 22992 |
rs754407933 | in-del | -/AG | | | intron-variant | KDM2A | GRCh38.p7 | 11:67175418 | CCCAGCCTAGATGAC[-/AG]AGACTCTGTCTCCGA | 22992 |
rs754442344 | snp | A/C | 2.73116e-05 | 0.00369527 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255075 | CACCCAGCCCAGATT[A/C]AACAGGAAACCGATC | 22992 |
rs754459566 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67205289 | TCTGTCCATTGCCTT[A/G]CATTATTAGTTATGT | 22992 |
rs754467838 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67200360 | AGCTGGGACTACAGG[C/T]GTCCGCCACCACGTC | 22992 |
rs754470120 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67216164 | ACACCATTGGCACAG[C/T]ACTTAGTAAATCTCA | 22992 |
rs754526749 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67165694 | CTTGCTATCTCCCTT[A/G]ATTCACTTAAAGACT | 22992 |
rs754544829 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67136351 | GAGCATACTTAAGTT[A/C]TACTGCCTCTTCATC | 22992 |
rs754563375 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67179469 | GTAGAGACATGGTTT[C/G]TCCGTGTTGGTCAGG | 22992 |
rs754577818 | snp | A/G | 6.66689e-05 | 0.00577321 | intron-variant | KDM2A | GRCh38.p7 | 11:67181287 | GTTTTTAATTATACC[A/G]CTTATCTTTCTAATA | 22992 |
rs754593912 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67151123 | GACCAATTATGCTGA[A/C]AATACAGAACTGTTT | 22992 |
rs754604759 | snp | A/C | 0.000162827 | 0.00902146 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255472 | AAACGGCCCTGTCTC[A/C]ATGGCCAGGTTCTTG | 22992 |
rs754616197 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67254670 | AGCCTTGCAGCCCTT[G/T]TGCTTGTTGTCATAT | 22992 |
rs754617165 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67152734 | TAAGTACTTCTTTTA[C/T]CTTGCTGTAGAATTT | 22992 |
rs754679673 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67244061 | CCAGGGGTGTTTAGG[C/T]AGAATATAAAGGTAT | 22992 |
rs754688807 | snp | A/G/T | 9.18316e-05 | 0.0067755 | intron-variant | KDM2A | GRCh38.p7 | 11:67252591 | CACTTGTAGAAGAAC[A/G/T]AGCCTCCAGGTACTC | 22992 |
rs754731952 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67173517 | CTGTTTTGGCCTCCC[A/T]TTGTGCTGGGATTAC | 22992 |
rs754737997 | in-del | -/T | 2.27503e-05 | 0.00337263 | intron-variant | KDM2A | GRCh38.p7 | 11:67219284 | CTGTTCCCCTTCTCC[-/T]TAGGCTGGATTCATG | 22992 |
rs754746572 | snp | G/T | 1.72145e-05 | 0.00293376 | intron-variant | KDM2A | GRCh38.p7 | 11:67245160 | TAAAGCAACCTGATA[G/T]ATTTGACCTCACTGC | 22992 |
rs754791786 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67162686 | GCTGGGATTACAGGC[A/T]TGAGCCACCGCGCCC | 22992 |
rs754794636 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67225345 | ATGCGTGATGTTAAC[A/G]TCATTCTTGGGCAGG | 22992 |
rs754821451 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67186965 | AAAAGCTAATAACTA[A/G]TAGGGGCACAGTATA | 22992 |
rs754826885 | snp | C/G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67209529 | GCTCACTGCAGCCTC[C/G/T]GCCTCCCAGGTTCAA | 22992 |
rs754834409 | snp | A/G/T | 3.31281e-05 | 0.00406978 | intron-variant | KDM2A | GRCh38.p7 | 11:67215967 | ATGGTCATAGTTGTG[A/G/T]TAGGGGTTGGAATCT | 22992 |
rs754890883 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67240709 | CCCGCACTCCACCCC[C/T]GCTCTCCTATCCCAA | 22992 |
rs754897094 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67145378 | GCCTGTAATCCCAGC[C/T]ACTTGGGATGCTGAG | 22992 |
rs754924206 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67227034 | ATTAATCTGTGCTGA[G/T]TTGTCCTTTCCTGGA | 22992 |
rs754925482 | snp | C/T | 1.75019e-05 | 0.00295815 | missense, nc-transcript-variant, utr-variant-5-prime | KDM2A | GRCh38.p7 | 11:67217756 | TCATCCCCCCTACAG[C/T]CCACAACCTGGAGCT | 22992 |
rs754925766 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67175372 | AGGTCAAGGGTCAAG[C/G]CTACAGTGAGCTGTG | 22992 |
rs754963206 | in-del | -/AC | | | intron-variant | KDM2A | GRCh38.p7 | 11:67213353 | TCTCGAGTTTTACCT[-/AC]CTGGAGTTCATTGGT | 22992 |
rs754986673 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67196745 | TTAAAACGGCCATAG[-/T]TTTCAGTTTTATAAG | 22992 |
rs754987680 | snp | A/G | 4.96816e-05 | 0.00498381 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67254359 | CAGATCAGTCCTCCA[A/G]TCTACTCACTGCTGT | 22992 |
rs755021636 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67251074 | TTGCGGGATAGATTT[A/G]TAGTCTGTGATAAAA | 22992 |
rs755067842 | snp | C/T | 1.66785e-05 | 0.00288773 | synonymous-codon, intron-variant | KDM2A | GRCh38.p7 | 11:67250529 | CCTTCGCCATTCCCC[C/T]CGTGTGCTAGTGCAG | 22992 |
rs755080430 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67196125 | TTGAGGAGCAACGAC[A/G]TAGTCACCCATATTA | 22992 |
rs755090126 | snp | C/G | 1.65669e-05 | 0.00287805 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67231793 | TCCCACAATGGACAA[C/G]TGTGGGATCCCCAGT | 22992 |
rs755094781 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67211762 | CTGTCACTTCTCACT[G/T]TATATCCTCAAGTTC | 22992 |
rs755105510 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67249655 | CTGCTTTATTATTCA[C/T]GTGGGGGTTGGAGTG | 22992 |
rs755105655 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67133348 | CTCAAGTGATCCACC[C/T]GCCTTGGCCTCCCAA | 22992 |
rs755109934 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67236555 | TCTGGCGGCCCAGCT[A/C]ACTTAATAAAGCAAA | 22992 |
rs755177983 | snp | C/G | 1.81651e-05 | 0.00301368 | intron-variant | KDM2A | GRCh38.p7 | 11:67231996 | ATGACAGCTACTGAT[C/G]CAGCTATGGCAGTCA | 22992 |
rs755213693 | snp | A/C | 1.67919e-05 | 0.00289753 | intron-variant | KDM2A | GRCh38.p7 | 11:67253408 | ACGGCTCTGAGTATG[A/C]TGGGAAACAGTGTAT | 22992 |
rs755228952 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67151579 | TGGTCTTGAACTCCT[C/G]ACCTCAGGTGATCTG | 22992 |
rs755241965 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67183391 | GTGGTCCACAGATGA[C/T]CTGCATCAGAATTGC | 22992 |
rs755265889 | snp | C/T | 6.82536e-05 | 0.00584141 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67207507 | ATGCATCTTTTATGG[C/T]AGGGAGTCGTCGCAT | 22992 |
rs755267187 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67119862 | CCTCCGACTCCCGGT[C/T]TCCAAAGCCAGAAGA | 22992 |
rs755274824 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67170578 | CTACCACACCGGGCT[A/G]ATATTTTTGTATTTT | 22992 |
rs755283965 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67181945 | AGATTTAAGACTTAG[A/G]ACTGAATTAAATCTC | 22992 |
rs755287814 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67154888 | TATTCCGTTGTATGG[A/G]TATACCACATTTTGC | 22992 |
rs755295086 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67132579 | GGCATGAGCCGCTGC[A/G]TCCAGCCAGTTTGTT | 22992 |
rs755301684 | snp | C/T | 3.31219e-05 | 0.00406938 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67253527 | TCCAGCTGCCCCCTT[C/T]TCAGGACCCTTGATC | 22992 |
rs755302902 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67197782 | TGAAGTGCTTAGAAC[A/G]GTGTCTGGCATATAC | 22992 |
rs755328564 | in-del | -/G | 1.66269e-05 | 0.00288326 | intron-variant | KDM2A | GRCh38.p7 | 11:67254527 | GATTGACCCACATCA[-/G]GCTCATTTCTTCACA | 22992 |
rs755347015 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67256696 | AACTGCACCCTTGCC[A/G]CTTCCAAAGCAATAG | 22992 |
rs755362843 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67184368 | GGTGCGGTGGTTGAC[C/G]CCTGTAATCCCAGCA | 22992 |
rs755378342 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67205328 | TAATATATATATTCT[A/G]CCTTGTCTATTTCAC | 22992 |
rs755378900 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67168225 | AGGAGCAACACAGTC[A/T]GTATCTATGGTCTTT | 22992 |
rs755410285 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67169680 | TGCGCTCAGCCCATC[A/G]CTTGGTTTCTTTTTT | 22992 |
rs755438131 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67122254 | ATTTTAGACTGAATT[C/T]AGGAGAAAAAGAATG | 22992 |
rs755452372 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67243769 | GCAGTGAGCCGAGAT[C/T]GCACCATTGCACTTC | 22992 |
rs755455446 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67125093 | GTCTCGATCTGCTGA[C/G]CTCGTGATCCGCCTG | 22992 |
rs755464633 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67140847 | TTATTTATTGGGTCT[A/G]CTTTATGAAGAACCT | 22992 |
rs755483626 | snp | C/T | 1.70685e-05 | 0.00292129 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67250157 | CCTGCGGAGCTGCGA[C/T]GAGCCTCTCACGCCC | 22992 |
rs755510836 | snp | A/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67177907 | GATGTCCTGATGGCA[A/G]CAGTGTCACTAAGAG | 22992 |
rs755518469 | snp | C/T | 1.65669e-05 | 0.00287805 | intron-variant | KDM2A | GRCh38.p7 | 11:67228029 | TTCTCTATTTTATTC[C/T]TCTGTAGGTTCCAAA | 22992 |
rs755557910 | snp | C/T | 6.49773e-05 | 0.00569951 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67248286 | CTTCCTATAGATGGA[C/T]GGAGAGGGGTTGCTT | 22992 |
rs755577598 | snp | C/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206464 | TAAATAGGCTGGGCA[C/T]GGTGGCTCACGCCTG | 22992 |
rs755581368 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67190207 | CTGAGGTGAGGAGTT[C/T]GAGACTAGCCTGGCC | 22992 |
rs755603452 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67213427 | TGTAAAATGTTGCGT[A/G]TTGCTTTCACTTCTC | 22992 |
rs755603881 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67257172 | GCCGGGAGAGTGCCT[C/T]TGACTTTGGGACATT | 22992 |
rs755643316 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67245647 | ACTAAAAATCCGATT[C/T]AATCTTTAGGCTTTA | 22992 |
rs755654233 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67127525 | AGATGTTATTATCGC[A/G]TGTTCAATCCTGTTA | 22992 |
rs755666005 | snp | A/G | 3.34622e-05 | 0.00409023 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67254927 | CGGCGCATTGCCAAC[A/G]TCACCTTGATCGACC | 22992 |
rs755671431 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67177102 | GTCTCTACAAAAATA[C/T]AAAAATTAGCCGGGC | 22992 |
rs755685086 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67229507 | AATCTTTAATCCAAG[C/G]AAGATATTTTTTGCT | 22992 |
rs755707103 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67191526 | ATTTATTCCTGGAAT[A/G]GATGATTTGACATGT | 22992 |
rs755708197 | in-del | -/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67172008 | TCTTCTTTTTTCTTT[-/G]GAGGCAGGATCTCAC | 22992 |
rs755720957 | in-del | -/G | | | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67238915 | AGAAACTCAACCAGA[-/G]GTGTGCACCCTCCTT | 22992 |
rs755724216 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67149257 | GTGACCTTGAACAGG[A/G]TACTTCTTAACCTTT | 22992 |
rs755746042 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67135645 | ATATATTCATAAATG[A/T]AGTGATCGTTTTATA | 22992 |
rs755754130 | snp | C/T | 8.29098e-05 | 0.00643801 | intron-variant | KDM2A | GRCh38.p7 | 11:67228005 | TCTTTCCTTGAAAAT[C/T]GTCATCTTTTCTCTA | 22992 |
rs755758869 | snp | A/C | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185795 | AGCATGAGTTCGGCC[A/C]CTTCGTGCTTTCTCT | 22992 |
rs755773965 | in-del | -/TTTTGTTTTT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67145984 | TCTTCCCGTTTTTTG[-/TTTTGTTTTT]TTTTGTTTTTTTTTT | 22992 |
rs755822671 | snp | A/G | 5.06586e-05 | 0.00503257 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255065 | AGCTAAGACACACCC[A/G]GCCCAGATTCAACAG | 22992 |
rs755831084 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67221109 | AGTGTTGTTTGCTGG[C/G]TAGCCTCCACCTTAG | 22992 |
rs755846768 | snp | C/T | 0.000133007 | 0.0081539 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | KDM2A | GRCh38.p7 | 11:67180084 | TCTTTCCTAGCGTGG[C/T]ACCATGCGACGACGC | 22992 |
rs755850347 | snp | C/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67179356 | TTGGCTCACTGCAAC[C/T]TCCACCTCCCAGGTT | 22992 |
rs755880113 | snp | G/T | 1.65471e-05 | 0.00287633 | missense, intron-variant | KDM2A | GRCh38.p7 | 11:67250727 | GCGGGAGGTCTGGAT[G/T]TCTGTCTTCCGCTAC | 22992 |
rs755885873 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67134731 | GCTGGTCTCGAACTT[A/C]TGACCTCAGGTGATC | 22992 |
rs755889719 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67128632 | ACATCAGTCTTCCAC[A/G]GTAAGCTATATTTTG | 22992 |
rs755931673 | snp | C/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185877 | CTCACCAGATGCTGG[C/T]GCCTTGATTTTAGAC | 22992 |
rs755936661 | snp | A/T | 0.000102331 | 0.00715229 | intron-variant | KDM2A | GRCh38.p7 | 11:67181282 | TTATCGTTTTTAATT[A/T]TACCACTTATCTTTC | 22992 |
rs755938906 | snp | C/T | | | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67239628 | GGGCGACCCCCTCTA[C/T]TTGCTGAGAGGGGAG | 22992 |
rs755948634 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67122516 | ATTTTTAGTAGAGAA[C/T]AGGGTTTTACCATGT | 22992 |
rs755958755 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67223427 | TTTATTTTTGACACA[A/G]GGTCTCACTCTGTCA | 22992 |
rs755961484 | snp | C/T | 1.7139e-05 | 0.00292732 | intron-variant | KDM2A | GRCh38.p7 | 11:67252582 | ATCCCTGTACACTTG[C/T]AGAAGAACGAGCCTC | 22992 |
rs755968016 | snp | C/T | 1.65982e-05 | 0.00288077 | intron-variant | KDM2A | GRCh38.p7 | 11:67242995 | TTTTTCCTTCTTTTC[C/T]CTCCTACCCTTAGAT | 22992 |
rs755988449 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67137627 | AGTTCTTTTATTGAA[A/G]TAGGGTACACTGAAG | 22992 |
rs755993063 | snp | C/G | | | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67238425 | TTTCCAAGAAGACCT[C/G]TCAATAGCTAGATCA | 22992 |
rs756016013 | snp | A/G | 0.000134212 | 0.00819074 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | KDM2A | GRCh38.p7 | 11:67215378 | CAACATGTGGCCAAG[A/G]CACTTGAAGGAAAGC | 22992 |
rs756052829 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67186734 | TGAGTGTAGCCCCAC[A/G]TTTTATTTTGTACAT | 22992 |
rs756058513 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67128254 | GTGATCCTCTCTCCT[G/T]CCTGGAGGCCTCTCC | 22992 |
rs756063226 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67240621 | TCTCTTTCCCTTCCT[G/T]TGATCTGTAGGGTGT | 22992 |
rs756078975 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67158762 | CCAAAGTGCTCGTAT[A/T]ATAGGCGTGAACCAC | 22992 |
rs756112703 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67136171 | TGTGCTTGGTACTGG[C/T]ATTTTCGATATACTC | 22992 |
rs756157230 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67207735 | TGTCACCAAAAGGGT[G/T]GTTTTCGGCTGGACG | 22992 |
rs756174161 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67193620 | AATCCCGGCACTTTG[A/G]GAGGCTGAGGCAGAC | 22992 |
rs756179125 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67212801 | AAAAAAAAAATACTC[-/A]ATATGTTCTGAACCG | 22992 |
rs756195118 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67208218 | AATAAATTTTAAAAT[A/T]TTAAAATTTATTATT | 22992 |
rs756208040 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67209030 | AACCTCTGCCTCCCC[A/G]GTTCAAGCAATTCTC | 22992 |
rs756226409 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67225092 | CTTGGCCTCCCAAAG[C/T]GCTGGGATTACAGGT | 22992 |
rs756229891 | snp | C/T | 1.74543e-05 | 0.00295412 | intron-variant | KDM2A | GRCh38.p7 | 11:67254467 | CCCCCTGCCTCCAGC[C/T]CTCCCTGGAACTTGA | 22992 |
rs756231877 | snp | C/T | 3.34499e-05 | 0.00408948 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67250305 | GATGAGCGCTTCAAA[C/T]GGCGGCAGTTGCTGC | 22992 |
rs756232904 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67249515 | ATAGTGGGCTCCAGG[A/G]AAAGACAAGTATCTA | 22992 |
rs756235125 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67198710 | GTGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAG | 22992 |
rs756248993 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67123919 | TGACCTCAGATGATC[C/T]GCCTGTCTTGGCCTC | 22992 |
rs756277510 | snp | A/G | 2.00479e-05 | 0.003166 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67231638 | AACCCCGACGCTTGA[A/G]CAGCAGGCGTTCTGT | 22992 |
rs756291502 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67173412 | CATGCGTGAGCCACC[A/G]TTCTTGGCCTAATTT | 22992 |
rs756312652 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67177111 | AAAATACAAAAATTA[A/G]CCGGGCATATTACTC | 22992 |
rs756314411 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67131090 | ACTACTTTGCAAGGC[C/T]GAGGCGGGCAGATTG | 22992 |
rs756321923 | snp | C/T | 1.65971e-05 | 0.00288067 | synonymous-codon, intron-variant | KDM2A | GRCh38.p7 | 11:67250373 | GGAGAACAATCCCAG[C/T]GGCAAAAAGGAGCTG | 22992 |
rs756346308 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67234054 | TCAAAATGTAGCTGA[C/T]GTCAGAAGACAACAG | 22992 |
rs756365230 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67144472 | GGTCAGGCTGGTCTT[A/G]AACTCCTGACCTCAG | 22992 |
rs756370480 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67194487 | GATCAGGAGTTATAT[A/G]TACTGTGGACCCTGA | 22992 |
rs756388479 | snp | A/C | 0.000561535 | 0.0167467 | intron-variant | KDM2A | GRCh38.p7 | 11:67196349 | CTCACTGTGTTGCCC[A/C]AGCTGGCCTTGAAAT | 22992 |
rs756389855 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67248428 | CATCAAATGTGGGGG[A/T]TTGCTACACGTTTGC | 22992 |
rs756455466 | snp | A/G | 1.67094e-05 | 0.0028904 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67231921 | GAAATGTGTCCCCAC[A/G]GGGATAGAAGATGAA | 22992 |
rs756491143 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67195963 | TCCACAATATCTTCT[A/G]TCAACTCAAGATGTT | 22992 |
rs756503460 | in-del | -/CTCTCTCTC/CTCTCTCTCTT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67169760 | TCTCTCTCTCTCTCT[-/CTCTCTCTC/CTCTCTCTCTT]TTTTTTTTTTTTTTT | 22992 |
rs756528316 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67217087 | TCTCTACTAAAAATA[C/T]AAAAATTAGCTGGGT | 22992 |
rs756541399 | snp | A/T | 0.000102932 | 0.00717324 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67207503 | ATCGATGCATCTTTT[A/T]TGGCAGGGAGTCGTC | 22992 |
rs756548279 | snp | C/T | | | upstream-variant-2KB, missense | KDM2A, LOC107984341 | GRCh38.p7 | 11:67117788 | CCCCAGAGCAAGAGA[C/T]TGGCTGGGGAAATGC | 22992 |
rs756559671 | snp | A/G | 3.67924e-05 | 0.00428892 | intron-variant | KDM2A | GRCh38.p7 | 11:67252905 | GGGCCCAGAAGAAGC[A/G]GGCAAGAAAAGTTGC | 22992 |
rs756586604 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67151225 | TTGGTTCTGCTGCTG[C/T]TTCCAACAGCCTAGA | 22992 |
rs756606426 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67154659 | GGCCAGGCTAGTCTC[A/G]AACTCTTGGCCTCAG | 22992 |
rs756608567 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67204209 | TTTTTTTCTTTTTGC[A/G]TAGAACATTTCATTG | 22992 |
rs756609261 | snp | C/G | 3.3123e-05 | 0.00406945 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67253508 | AGTCTCTGCCCTCAG[C/G]ACCTCCAGCTGCCCC | 22992 |
rs756610326 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67234884 | GGGCATGGTGGCTCA[A/T]GCCTGTAGTCCCAGC | 22992 |
rs756613974 | snp | C/T | | | upstream-variant-2KB, missense | KDM2A, LOC107984341 | GRCh38.p7 | 11:67117961 | GCTGCTGCCCCGTCG[C/T]TGACCCCCGCGCGAA | 22992 |
rs756621436 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67231387 | CAGGATCCTGTTTCT[A/G]CCTGTTAACTGTGAT | 22992 |
rs756648088 | snp | C/T | 1.65611e-05 | 0.00287755 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67246056 | AGAGACACAAGACTT[C/T]GAGAAGAAACTCATG | 22992 |
rs756651268 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67218136 | ACGTTTGGGCTCTGC[A/G]TTAGCCCTAGTAATT | 22992 |
rs756658349 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67167771 | CTATGTACTGTTGAT[C/G]TCTGTAGAATTTGAT | 22992 |
rs756686775 | in-del | -/CAG | | | intron-variant | KDM2A | GRCh38.p7 | 11:67202812 | TGTCGACCCGAGAAA[-/CAG]CAGCGAGATCTTGTA | 22992 |
rs756687479 | in-del | -/C | 1.82455e-05 | 0.00302033 | intron-variant | KDM2A | GRCh38.p7 | 11:67254478 | CAGCCCTCCCTGGAA[-/C]TTGATCAGTAAACCA | 22992 |
rs756700546 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67156147 | CAGCTACTTGGGAGG[C/G]TGAGGCAGAAGAATC | 22992 |
rs756719067 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67190001 | AATAGAAAAACAATA[A/G]AGAAAAGTCAAAGAA | 22992 |
rs756728371 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67243554 | CATGGTGGCTCACAC[C/G]TGTAATCCCAGCACT | 22992 |
rs756792405 | in-del | -/TG | | | intron-variant | KDM2A | GRCh38.p7 | 11:67242281 | GTGGGTGTGTGTATG[-/TG]TGTGTGTGTGTGTGT | 22992 |
rs756805805 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67189136 | AAGTGTATGTAGGAC[A/G]TTTTCCAGGATACAC | 22992 |
rs756808280 | snp | A/G | 1.75419e-05 | 0.00296152 | intron-variant | KDM2A | GRCh38.p7 | 11:67252877 | GTGAGCAGCCCTGCC[A/G]CTGTCTTTCCAGGGG | 22992 |
rs756808483 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67139744 | AGACAGAGTCTCGCT[C/T]TGTCACTCAGTCTGG | 22992 |
rs756813047 | snp | A/C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67212252 | TGCCTAATGTTGACA[A/C/T]AAAAGAAATAATGAA | 22992 |
rs756813769 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67257815 | AGTCTTATGCTATCT[C/T]AGTTGACACATTGAG | 22992 |
rs756845143 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67205169 | TTGCTAGCACTCATT[A/G]TTTTCCATTTTTTAA | 22992 |
rs756846875 | in-del | -/TTTA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67187552 | ATTTAATTGATTTTA[-/TTTA]TTTATTTATTTATTT | 22992 |
rs756859861 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67257033 | GTTAATGACCTATAA[C/T]TGGAAGCTTCCTGCC | 22992 |
rs756883512 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67228939 | TCTGTTGCCCAGGCC[A/G]GTCTTAAACTCCTGG | 22992 |
rs756892467 | snp | C/G | 4.97244e-05 | 0.00498596 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67245987 | TGTCCTCTTGTAGCC[C/G]AGACTGCCTCACTCA | 22992 |
rs756914805 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67127442 | TCAATCTTGATGAAA[C/T]TGAGAGTTTTTAGCA | 22992 |
rs756942302 | in-del | -/AAAG | | | intron-variant | KDM2A | GRCh38.p7 | 11:67163441 | ATGACTTGGAATGAT[-/AAAG]AAGGACATTTAATGC | 22992 |
rs756945406 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67134853 | CAAAAGCAGTCTCAC[A/G]TTGTGTTTCCCACAT | 22992 |
rs756946962 | snp | C/T | 2.79497e-05 | 0.00373819 | intron-variant | KDM2A | GRCh38.p7 | 11:67219268 | TTTTCAGCCACTGCC[C/T]TCTGTTCCCCTTCTC | 22992 |
rs756952722 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67176899 | AGTAAATGCGAGGGC[C/T]TAAGACACTTTTGTA | 22992 |
rs756992763 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67214995 | GATACCTTCCAGACA[A/G]CACCTTTTATTGGAT | 22992 |
rs757032822 | snp | A/C | 4.97517e-05 | 0.00498732 | intron-variant | KDM2A | GRCh38.p7 | 11:67121362 | AGCCAGAGATTGGTT[A/C]GTATTTTCTCCCCCC | 22992 |
rs757034033 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67164315 | TTTTTGATTTCAGAT[A/G]TAAGAATTTTAGCTT | 22992 |
rs757041341 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67140614 | AAAAATTAGCCAGGC[A/G]TTGTGGCAGGCGCCT | 22992 |
rs757041459 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67126408 | AGACCCCCGTTTCTC[A/G]CACACAGATTGTTTT | 22992 |
rs757048302 | snp | A/G | 1.68354e-05 | 0.00290128 | intron-variant | KDM2A | GRCh38.p7 | 11:67180057 | GTGCATGATTTCATC[A/G]GTATGTTCCTTTCTT | 22992 |
rs757056005 | snp | A/G | 1.68066e-05 | 0.00289879 | synonymous-codon, intron-variant | KDM2A | GRCh38.p7 | 11:67250544 | CCGTGTGCTAGTGCA[A/G]CACTGCCCAGCCCGA | 22992 |
rs757077539 | snp | A/G | 4.71531e-05 | 0.00485534 | intron-variant | KDM2A | GRCh38.p7 | 11:67219448 | GAAGAGGTTTACTCC[A/G]GTTATGATAGATGTT | 22992 |
rs757080482 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67213287 | GTTTTTTATAACCAT[A/G]AGTTAGATATTTACC | 22992 |
rs757083484 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67162698 | GGCATGAGCCACCGC[G/T]CCCGGCCTGCGATTT | 22992 |
rs757084660 | snp | A/G | | | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67238181 | TATCTTTTATTCTCA[A/G]TTAGCAGGAGGGGGT | 22992 |
rs757106115 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67198066 | ATTTACTATCTTTTC[A/G]TCTTCATGATGAGTA | 22992 |
rs757107047 | snp | A/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67177538 | GTCGGGGTCATCAGT[A/G]TCACAGAGCGGCATC | 22992 |
rs757135411 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67251246 | TCTCCATTCAGTGAG[A/C]GAAGTGGGCATGCTT | 22992 |
rs757142092 | snp | A/G | 3.65197e-05 | 0.004273 | intron-variant | KDM2A | GRCh38.p7 | 11:67232002 | GCTACTGATCCAGCT[A/G]TGGCAGTCAGCTTCC | 22992 |
rs757170881 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67252683 | GCGAGTTCTCTTCCC[G/T]TCTATCACAGGTGCT | 22992 |
rs757191866 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67149119 | ATGGCAAAAGTTAAA[A/C]AGTGTTTTCTCTGTA | 22992 |
rs757205865 | in-del | -/CT | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185629 | TGGTGACGAGCGAAA[-/CT]CTGTCGCAAAAAAAA | 22992 |
rs757221240 | snp | A/G | 1.7386e-05 | 0.00294834 | missense, intron-variant | KDM2A | GRCh38.p7 | 11:67250672 | CCAGGCTGAATGGCC[A/G]GGGCAGTTGGGCTCA | 22992 |
rs757304455 | snp | A/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67184648 | GGTGAGTGGAGGGTG[A/G]CTATTGCCCACACCC | 22992 |
rs757306228 | snp | A/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206637 | GCTACTGTGGAGGTT[A/G]AGGCAGGAGAACTGC | 22992 |
rs757313193 | snp | C/G | 1.65608e-05 | 0.00287752 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | KDM2A | GRCh38.p7 | 11:67215916 | GGACTTTGGTGGTAC[C/G]TCTGTTTGGTATCAC | 22992 |
rs757323455 | in-del | -/TT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67140745 | CAAAAAGAGTGAAAC[-/TT]TGTCTCAAAAAAAAA | 22992 |
rs757329876 | snp | G/T | 1.74784e-05 | 0.00295616 | intron-variant | KDM2A | GRCh38.p7 | 11:67254193 | CTAGGCTCTTCTCTT[G/T]CCTGTACAGGTCAGG | 22992 |
rs757331718 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67135556 | TCCTGGATCACAGAC[A/G]TTAGCAACTTTTTTG | 22992 |
rs757339138 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67158238 | ATTTATGGTTCCTCC[A/G]TGTCTCTTTGTGGCT | 22992 |
rs757385627 | snp | C/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67120880 | TTCAGTGGTGCTTCA[C/T]CTGGTCAGCTCTCTG | 22992 |
rs757395421 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67220495 | TCTTACTTTAATTAT[A/G]TAAATGTATATACTG | 22992 |
rs757413598 | snp | A/C | 1.68553e-05 | 0.00290299 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67250192 | CTCATTCACCCACTT[A/C]CATGCTGCAGCTCAT | 22992 |
rs757421080 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67127738 | TTGAGATGGAGTTTT[A/G]CTCTTGTTGCCGAGG | 22992 |
rs757423293 | snp | C/T | 8.34885e-05 | 0.00646044 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67250289 | CCACAGTGCCAGCCG[C/T]GATGAGCGCTTCAAA | 22992 |
rs757435070 | snp | C/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185753 | CAGGGACTCCACTCT[C/T]ATGGGTGGGATTGGT | 22992 |
rs757471786 | snp | C/T | 1.65625e-05 | 0.00287766 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67254318 | CCTCCTGTCTCGACT[C/T]GACCTCAGTCACTGC | 22992 |
rs757493325 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67208065 | CGTTGTTTTTATACT[A/G]GGAAATTTTATAACT | 22992 |
rs757502650 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67137554 | TTTGAGGGTCAGTGT[-/A]AAAGGAGGTAAATAT | 22992 |
rs757513175 | snp | C/T | 2.10564e-05 | 0.00324465 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67231631 | GATCGAGAACCCCGA[C/T]GCTTGAGCAGCAGGC | 22992 |
rs757547026 | in-del | -/TATC | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67178695 | AATGTTTTCAGAGTT[-/TATC]TATGTCATGGCACAT | 22992 |
rs757560598 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67179689 | AGCTAATTTTAAATA[C/T]AGCTCTCCCTGTGAA | 22992 |
rs757560917 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67122327 | AGAGACTTCTTTATT[A/G]TTTATTTATTTTTAT | 22992 |
rs757579058 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67193489 | TAGAAACTCTAGTTT[G/T]AAAAGTTAATACACA | 22992 |
rs757594287 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67144089 | CTGGGATTATAGGTG[C/T]TCTCCACCACTCCTG | 22992 |
rs757596686 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67241503 | AGAATGAAAATACAT[A/G]AAAGTCCTGGTCTCC | 22992 |
rs757655739 | snp | A/G | 1.67385e-05 | 0.00289292 | intron-variant | KDM2A | GRCh38.p7 | 11:67181810 | TACTAGAGCAATTGT[A/G]TTTTCCATATATACT | 22992 |
rs757706599 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67132359 | CACGATCTCGGCTCA[C/G]TGTAACCTACGCTTC | 22992 |
rs757817902 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67240748 | TAGTGAAGGGTGGTG[A/G]CTTCTTTATATGGTT | 22992 |
rs757825247 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67130667 | GACACTCTTAATTAG[A/G]TTTCATTAATTTTCT | 22992 |
rs757834624 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67204115 | CTCCCCTACATTCTT[G/T]AAGGAAAGCATTTAC | 22992 |
rs757837817 | in-del | -/TT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67164407 | GATGTGATTATTAAC[-/TT]ACATTTTTAGTTTCT | 22992 |
rs757858520 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67165844 | GGCAAAAAGAAAGGT[C/T]ACTCTTACTTCCCCT | 22992 |
rs757872888 | snp | C/T | 1.66181e-05 | 0.00288249 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67252754 | TAAGGCCATTGTGCC[C/T]CAGGCCCTCAGTGGC | 22992 |
rs757881492 | in-del | -/TTAAAGCAACCTGA | 3.4659e-05 | 0.00416273 | intron-variant | KDM2A | GRCh38.p7 | 11:67245144 | CTACCCTATCCAGTC[-/TTAAAGCAACCTGA]TATATTTGACCTCAC | 22992 |
rs757908073 | snp | C/T | 1.67198e-05 | 0.0028913 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67245198 | TTCCAGCTTAAATTC[C/T]CCACTCGGCCAAAGG | 22992 |
rs757927887 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67230566 | AGGAGGTTGAGGCTG[C/T]AGTGAGCCATGATTG | 22992 |
rs757937345 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67202298 | TTAAAATAACAAGGT[A/G]TTTAGGATATTACAT | 22992 |
rs757946559 | snp | C/T | 1.6729e-05 | 0.00289209 | intron-variant | KDM2A | GRCh38.p7 | 11:67252597 | TAGAAGAACGAGCCT[C/T]CAGGTACTCTGCTTT | 22992 |
rs757953249 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67166616 | TGTAGTCCCAGTAAC[C/T]TGAGAGGCTGAGGCA | 22992 |
rs757962134 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255527 | CCATCACACTCTCCC[A/G]GCTTGCGCAGGAGGG | 22992 |
rs757968671 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67153101 | ACCATTCTCCTGCCA[C/T]ATTCTCCCAAGTAGC | 22992 |
rs758016927 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67139502 | CGCCCACCTCGGCCC[A/C]CCAAAGTGCTAGGAT | 22992 |
rs758044498 | snp | G/T | 1.66172e-05 | 0.00288242 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67252738 | TTGACTTGAGTAGGT[G/T]TAAGGCCATTGTGCC | 22992 |
rs758065371 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67213888 | GGGTTTTTTATTGAG[A/G]CAGTCTTGCCCTGTT | 22992 |
rs758089091 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67188996 | CAGTACCCCCTCTCA[A/G]TAATGGATAGAACAA | 22992 |
rs758090993 | in-del | -/GAGGTTGTGCT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67126179 | TGAACCCGCGAGACA[-/GAGGTTGTGCT]GAGCTGAGATCATGC | 22992 |
rs758126272 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67154500 | CGCAATGGCGTGATT[G/T]CAGCTCACTGCAGCC | 22992 |
rs758142606 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67196515 | TTAGCATAATGTGCT[A/G]TTTCCATTCACTGGA | 22992 |
rs758160239 | snp | G/T | 3.5137e-05 | 0.00419133 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | KDM2A | GRCh38.p7 | 11:67217787 | GTACGAGAATTGGCT[G/T]CTGTCAGGGAAACAG | 22992 |
rs758163838 | snp | A/T | 3.29788e-05 | 0.00406058 | intron-variant | KDM2A | GRCh38.p7 | 11:67219245 | AGAGAGACTTACTGT[A/T]ATGTGTGTTTTCAGC | 22992 |
rs758178167 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67125434 | GATCTGCCCGCCTTG[A/G]CCTCCCAACAAGTCA | 22992 |
rs758183880 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67133175 | TGCTATCTTGGCTCA[G/T]TGCAATCTCCGCCTT | 22992 |
rs758214841 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67251139 | AAGTCAGCTGAACTC[A/G]TCACATGTTGGTTGA | 22992 |
rs758215579 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67189923 | ACTTAAATAACTAGA[A/T]AAAGGACAAACTAAA | 22992 |
rs758217107 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67227234 | GCAGGCAAGCTGAGC[A/G]TCGATAGTGGAGAAA | 22992 |
rs758224814 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67147338 | ATGAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT | 22992 |
rs758327751 | in-del | -/AA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67182838 | GCACCCGGCTGGAAT[-/AA]AGTCTTTTTGAAATG | 22992 |
rs758360236 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67134737 | CTCGAACTTCTGACC[G/T]CAGGTGATCCACCTG | 22992 |
rs758371772 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67213016 | CGGCGGATGCTTGGT[C/T]AAAATTGTTGGCTCC | 22992 |
rs758387282 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67216952 | ACAACAACAAAAAAA[A/C]ATGAGGTCTTGTCCG | 22992 |
rs758425856 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67183581 | AAATTTCAGGGACAG[C/T]TTGGACAATAAAGTA | 22992 |
rs758447586 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67196373 | TTGAAATCCTGGACT[C/G]AAGCGATCTTCCTGC | 22992 |
rs758452624 | snp | G/T | 4.9889e-05 | 0.0049942 | intron-variant | KDM2A | GRCh38.p7 | 11:67242987 | TGCCCTGATTTTTCC[G/T]TCTTTTCCCTCCTAC | 22992 |
rs758453217 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67237857 | GAGGCTGAGGTCTAG[A/G]CTGTAGTAAGCTGTC | 22992 |
rs758461936 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67180451 | AGGAGTATTGTTGGA[-/T]TTTTTTTGCCTAACG | 22992 |
rs758479497 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67218666 | CTGGAGTGCAGTAGC[A/G]TGATCTTGGCTCACT | 22992 |
rs758483255 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67148929 | CTGGTGGCGCATAGC[A/T]CAGCATTACAGATCT | 22992 |
rs758502917 | snp | G/T | 0.00143996 | 0.0267938 | missense, nc-transcript-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67207514 | TTTTATGGCAGGGAG[G/T]CGTCGCATGGTGGAT | 22992 |
rs758571747 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67252474 | GTGGTCAAGTTATAT[A/G]CTATCAACATGTAGG | 22992 |
rs758577130 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67219760 | TCTCACTGCGTTGCC[C/T]AGGCTGGTCTAGAAC | 22992 |
rs758584187 | snp | A/G | 1.65627e-05 | 0.00287769 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67253546 | GGACCCTTGATCTTC[A/G]GTGGGCAGTAGGAAT | 22992 |
rs758584529 | snp | A/G | 1.92844e-05 | 0.00310513 | intron-variant | KDM2A | GRCh38.p7 | 11:67254167 | TGGATTAGAGAATTG[A/G]GAGTTTTGATCTAGG | 22992 |
rs758610304 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67151904 | CATGTACCACCACAC[C/T]GGGCTAATTTTTTTA | 22992 |
rs758617834 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67201246 | TGTGTATATATATAT[A/T]TTTCATAAGGCTATA | 22992 |
rs758631016 | in-del | -/TTTG | | | intron-variant | KDM2A | GRCh38.p7 | 11:67237607 | CAACCAACTCAGCTT[-/TTTG]TTTGTTTGTTTGTCC | 22992 |
rs758632696 | snp | A/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67120791 | TCCTCTTTTTACATA[A/G]TCAGTTTGCCCTTCT | 22992 |
rs758669036 | in-del | -/ATT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67196530 | ATTTCCATTCACTGG[-/ATT]ATTATTTAGCCTTAA | 22992 |
rs758682584 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67191841 | TCCTAACAGAGCAAT[G/T]AGGCAAAAAAAGGAA | 22992 |
rs758697579 | snp | A/G | | | missense, nc-transcript-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67207585 | TGGCTCAGTGGACAC[A/G]CTACTATGAGACCCC | 22992 |
rs758707689 | in-del | -/TATATAT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67203481 | ATTAATAATTATTAA[-/TATATAT]TAATATATTTTTATA | 22992 |
rs758722626 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67155343 | AGAGTCTCACCCTGT[G/T]GCCCAGGCTGGAGTG | 22992 |
rs758723766 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67171936 | CCACCCAGTCTTGAT[C/T]ACTATATGTTTATAG | 22992 |
rs758746652 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67157922 | TAGTGAGACCCCATC[A/G]CAAAAGAAAGAGAGA | 22992 |
rs758746844 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67140944 | AACTAGTTTAAAAAA[C/T]GCTATATTTTAATTA | 22992 |
rs758757180 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67134483 | TGCTATTCATTTTAT[A/G]ATTTTATTTTTTAAA | 22992 |
rs758776751 | in-del | -/TGT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67172647 | GTGTGTGTGTGTGTG[-/TGT]GGATTCCTTATAGTT | 22992 |
rs758811356 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67139945 | CTGACCTCAACTGAT[A/G]TGTGCATCTTGGCCT | 22992 |
rs758826301 | snp | C/T | 3.34622e-05 | 0.00409023 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67250272 | GCTGGCCCCAGCGAC[C/T]ACCACAGTGCCAGCC | 22992 |
rs758826343 | snp | C/G | 3.31592e-05 | 0.00407167 | intron-variant | KDM2A | GRCh38.p7 | 11:67228207 | AGACACCGCTTAGGT[C/G]TGAGGGTGAGGCCCG | 22992 |
rs758866132 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67156721 | GAGACTCCATCTCAA[-/A]AAAAAAAAAAAAAAA | 22992 |
rs758883518 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67175917 | CTTCAGAGACACATA[C/T]ACAAAATAAGGTGAG | 22992 |
rs758889710 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67128752 | GCTTTCCACTAGAGT[A/G]TAAGCTTCTTGAGAG | 22992 |
rs758893111 | snp | C/T | 2.16828e-05 | 0.00329256 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67231627 | AGTGGATCGAGAACC[C/T]CGACGCTTGAGCAGC | 22992 |
rs758938581 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67173053 | TGGAGTGCAGTGGTG[C/T]TGTAACAGTTCACTG | 22992 |
rs758960774 | in-del | -/TA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67143002 | TGTAAACACTTCAGT[-/TA]TATATATATATCTAT | 22992 |
rs758990522 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67193314 | ACTTTCAACAATCTG[A/T]TGGGTATGAAAGAGA | 22992 |
rs759002120 | snp | A/G | 1.6784e-05 | 0.00289685 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67250244 | GGGTATGGTGACTCG[A/G]TCATCCCCTGGGGCT | 22992 |
rs759018231 | snp | C/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67177952 | GTTCTACTGTAATCT[C/T]ATGGGAACACTGTCA | 22992 |
rs759021837 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67257665 | CTCCTAAAGTCACTT[A/T]TGTTTAAAGGGTTTG | 22992 |
rs759061655 | in-del | -/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67235886 | GCCTCCCAAAGTGCT[-/G]GGATTACAGGCGTGA | 22992 |
rs759083799 | snp | A/G | 1.66549e-05 | 0.00288568 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67250337 | GCTGCAGGCCACAGA[A/G]CGCACCATGGTACGG | 22992 |
rs759102277 | in-del | -/AAAA | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67178419 | CAGAAAATAAAAAAT[-/AAAA]TAAAGTGTACAATCC | 22992 |
rs759108896 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67210577 | ATTAACATTAAAGGG[C/T]GGAGAAGAACCTATG | 22992 |
rs759129353 | snp | A/C/G | 0.000405871 | 0.0142402 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67231620 | AGGAAGCAGTGGATC[A/C/G]AGAACCCCGACGCTT | 22992 |
rs759152414 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67236099 | CTAATAGCAGGGCAC[A/G]ATAGGATAGTAGTAG | 22992 |
rs759174639 | in-del | -/ATAC | | | intron-variant | KDM2A | GRCh38.p7 | 11:67193862 | TGAGACCCCATCTCA[-/ATAC]ATACATACATACATA | 22992 |
rs759178456 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67149806 | GCTCACTGCAACCTC[G/T]GCCTCCCAGGTTCAA | 22992 |
rs759185120 | snp | C/T | 1.66109e-05 | 0.00288187 | intron-variant | KDM2A | GRCh38.p7 | 11:67181905 | TGGGTAAGTGTCGAG[C/T]TTTTGGCCTCTGTCT | 22992 |
rs759189998 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67180940 | GTGCTGGGATTACAG[A/G]TATGAGCCACCACAC | 22992 |
rs759226319 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67154383 | GTTTTGCAATCATCA[C/T]CTCTGGCTTTCTGTC | 22992 |
rs759242617 | in-del | GAGATGGAGCATCTCTCTTGG/TTTGGTGTTTCCTTTTT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67192462 | TTTTTTTTTTTTTTT[lengthTooLong]TGCCCTGACTGGAGT | 22992 |
rs759257864 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67204848 | TTAGTACTTCATTCC[C/T]TTTTATGGTCGACTA | 22992 |
rs759267538 | snp | A/G | | | upstream-variant-2KB, utr-variant-3-prime | KDM2A, LOC107984341 | GRCh38.p7 | 11:67117552 | CGTCCTCCTGAAAGA[A/G]TTGATGGCTGTTTAT | 22992 |
rs759275743 | in-del | -/GAG | | | cds-indel, intron-variant | KDM2A | GRCh38.p7 | 11:67250607 | GGAGAGGAGGAGGAA[-/GAG]GAGGAGGAGGAGGAG | 22992 |
rs759316504 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67256089 | CCAGTGGCTCACTGA[A/G]CTTTCAGGGCAGTCA | 22992 |
rs759331097 | in-del | -/AAGT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67139188 | TAACCAAGCCAGGGC[-/AAGT]AAGTGTACCCTGCAG | 22992 |
rs759347527 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67203875 | GTGCGATCTTGGCTC[A/G]CTGCAACCTCTGCCT | 22992 |
rs759356918 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67257444 | TTGGGGGACAGAGGA[A/G]CCTGGGGAGTCCATC | 22992 |
rs759367355 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67168524 | TTTTCTATATTCAGC[A/G]TGGTCTTGTATGAAT | 22992 |
rs759377584 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67252575 | AGGTGTGATCCCTGT[A/G]CACTTGTAGAAGAAC | 22992 |
rs759380884 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67169118 | CTGCCACCGCGCCTG[A/G]CCAATTTTTGTATTT | 22992 |
rs759386681 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67242031 | GTGAGCCGAGATAGC[A/G]CCACTGCACTCCAGC | 22992 |
rs759397670 | snp | C/T | 5.23273e-05 | 0.00511477 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67207477 | AGGATATTAGTGGCT[C/T]GATAGAGATGATCGA | 22992 |
rs759414049 | snp | C/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67120886 | GGTGCTTCACCTGGT[C/T]AGCTCTCTGGAGATA | 22992 |
rs759438603 | snp | A/G | 1.75139e-05 | 0.00295916 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67252846 | TGACATGGCTCGTCA[A/G]TAGGCTGCCAGGTAA | 22992 |
rs759456819 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67140465 | CTTAAAAGAAGTTAC[A/G]AGTAGGCCTGGTGCG | 22992 |
rs759457654 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67139301 | CCAGGCTGGAGTGCA[A/G]TGGCATGATCTCAGC | 22992 |
rs759465822 | snp | C/T | 1.65608e-05 | 0.00287752 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67228117 | GTACTGCATAACCAA[C/T]CGTTCCCACCTAACT | 22992 |
rs759507489 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67243282 | ATCTTTGGAGGTGAC[C/T]TCTCTTAACAGAACT | 22992 |
rs759516537 | snp | C/T | 1.91239e-05 | 0.00309218 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255010 | CTTGTCCATCAACAG[C/T]CTCTACTGCCTGTCT | 22992 |
rs759525288 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67189819 | ACTCCAGCCGGGGCA[A/G]CAAAGTGAGACTCTG | 22992 |
rs759528906 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67212954 | GAAACAGTAAATTTT[A/C]TTTGAAGGAAAGAAA | 22992 |
rs759545638 | snp | A/G | 1.69241e-05 | 0.00290891 | intron-variant | KDM2A | GRCh38.p7 | 11:67180034 | CACTTGTAGGTAGGC[A/G]TGAAAAAGTGCATGA | 22992 |
rs759583822 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67155213 | TAGAGATGGGGTTTT[C/G]CTATGTTGGCCAGGC | 22992 |
rs759596628 | snp | A/G | 1.71708e-05 | 0.00293003 | missense, intron-variant | KDM2A | GRCh38.p7 | 11:67250651 | GTGCAGAGGAGGGGG[A/G]TGCAGCCAGGCTGAA | 22992 |
rs759629837 | snp | A/T | 1.76786e-05 | 0.00297305 | intron-variant | KDM2A | GRCh38.p7 | 11:67180234 | TCAGTATTGTTTTGG[A/T]TCCAGCTTACAGTCC | 22992 |
rs759634840 | in-del | -/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67121707 | TAGAATATAAATTTT[-/G]GGGGCAAAGCTGTTT | 22992 |
rs759640089 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67127189 | TGTAGCCTCAACCGC[A/C]TGGCTCAAGTGGTCC | 22992 |
rs759643216 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67221832 | CCTAGCTACTGGGGA[G/T]GCTGAGGTGAGAGGA | 22992 |
rs759646132 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67191217 | ATTTTAGTAGAGATG[A/G]GGTTTCACCATGTTG | 22992 |
rs759671755 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67123276 | GCCACAGTACCTGGC[-/T]TTTTTTTTTTTTTTT | 22992 |
rs759678206 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67163749 | TAATCCCAGCTACTC[C/G]GGAGGTTGCAGCAGG | 22992 |
rs759678506 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67134662 | GGTATGCGTCGCCAC[A/G]CCCAGCTAATTTTTA | 22992 |
rs759724832 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67197357 | TTTTGTATTTTTTTT[A/G]TAGAGATGGGATTTT | 22992 |
rs759752726 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67164839 | CCTGATCTCAAGTGA[A/T]CTACCCACCTCGGCC | 22992 |
rs759766452 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67137866 | GCAGTGGTGCGATCT[C/T]GGCTCACTGCAACCT | 22992 |
rs759791317 | in-del | -/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67210664 | TACGGGGACCTAAAA[-/C]ATGAAAGATTGAATG | 22992 |
rs759812974 | snp | C/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67184553 | GAATTGCTTGAACCG[C/G]GAGGCAGAGGTTGCA | 22992 |
rs759824179 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67218192 | TCTGCAGGTGATACA[C/T]AATCTATGTTGAAGA | 22992 |
rs759828476 | in-del | -/AAA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67156719 | GCGAGACTCCATCTC[-/AAA]AAAAAAAAAAAAAAA | 22992 |
rs759833989 | snp | G/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185343 | GCTATAGGTTAAATG[G/T]TATCCCTGCCAGGTG | 22992 |
rs759849224 | snp | C/T | 1.67758e-05 | 0.00289614 | intron-variant | KDM2A | GRCh38.p7 | 11:67242963 | GGGTGGTTGGCTCTT[C/T]GTTCACCCTGCCCTG | 22992 |
rs759852237 | in-del | -/TC | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67257422 | TGGAGGAAAGAAGTG[-/TC]TCTCTGTTGGGGGAC | 22992 |
rs759886194 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67214711 | TCCTGGGTTCAAGTG[A/G]TCTTCCCACCTTGGC | 22992 |
rs759915301 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67157676 | CTGGAACTGGGGAGG[C/T]GGGGTTTGCAGTGAG | 22992 |
rs759935290 | snp | A/G | 1.65718e-05 | 0.00287848 | synonymous-codon, nc-transcript-variant, intron-variant | KDM2A | GRCh38.p7 | 11:67243083 | AGTACAGTGGCCAAA[A/G]AGGGATAAGGTAAGA | 22992 |
rs759947655 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67134145 | GGGGAAAGATTTTTT[C/G]AAACTTTGAGGAGAG | 22992 |
rs759948645 | snp | A/C/G | 3.89858e-05 | 0.00441494 | intron-variant | KDM2A | GRCh38.p7 | 11:67254160 | TTGAAGCTGGATTAG[A/C/G]GAATTGAGAGTTTTG | 22992 |
rs759952922 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67237678 | CTAGGCCAGATGTGT[A/T]AGCTCATGCCTATAA | 22992 |
rs760009714 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67172763 | CCATAGCTAGAAATT[A/T]CTTGCCTAACTGCCC | 22992 |
rs760021762 | snp | A/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67186380 | GGAAAACAAAACAAA[A/G]CTGTCAACCAAGCAT | 22992 |
rs760047829 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67154815 | ACTTAGCATATGTTC[A/G]AGGTTCATCTGTGTT | 22992 |
rs760059161 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67203400 | AAGTAGTCTGAAAAT[A/G]CAAAATAGTCTAGTA | 22992 |
rs760065003 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67237015 | GCACAGAGAAAATGA[C/G]TGAGAGTGGCAGAGT | 22992 |
rs760097937 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67171723 | AGAAAAACTATTTGA[C/T]ACAAACTAGGTCTCA | 22992 |
rs760135764 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67157079 | AGCACTTTGGGAGGC[C/T]GAGAAGGGCCGATCA | 22992 |
rs760166745 | snp | C/T | 0.000217641 | 0.0104294 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67254219 | TCAGGACAATCGCAG[C/T]AAGCTCCGGAACATG | 22992 |
rs760178349 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67135132 | GGAGTGCAATGGCGC[A/G]ATCTCGTCTCACCAC | 22992 |
rs760197185 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67143490 | AGCAAATACCTGTGT[A/G]ACTACTACTCAGTCA | 22992 |
rs760208776 | snp | A/C | 1.66554e-05 | 0.00288573 | intron-variant | KDM2A | GRCh38.p7 | 11:67253632 | CTCTGGACCTGACTT[A/C]TCTGTGCTTGTCTTG | 22992 |
rs760209615 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67248761 | AGCAGTGTACTTGAG[A/C]TTCCAGTTAAGCAGG | 22992 |
rs760209706 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67180722 | CAGTGGTGCGATCTC[A/G]GCTCACTGCAACCTC | 22992 |
rs760213359 | in-del | -/AAAAAAAAA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67195370 | TGAGACTCCGTCTCC[-/AAAAAAAAA]AAAAAAAAAAAAAAA | 22992 |
rs760251726 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67123182 | GGTCTTGCTATGTTG[C/T]CCACCCTAGTCTTGA | 22992 |
rs760252629 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67175847 | GGGAAACTATACTTA[C/T]TCTAGTAGCATTGCT | 22992 |
rs760260853 | snp | G/T | 3.35801e-05 | 0.00409743 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67250231 | CGGTTTCCCCCCGGG[G/T]TATGGTGACTCGGTC | 22992 |
rs760282964 | snp | C/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67207023 | TGTTTAACAAAAGAA[C/T]ATAAATTCAAAATCA | 22992 |
rs760283906 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67232777 | CAATGGCAAGATCTC[A/G]GCTCACTGCAACCTC | 22992 |
rs760300632 | snp | C/T | 0.000242106 | 0.0109997 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67250143 | AAAGTCCTGCGGCCC[C/T]TGCGGAGCTGCGATG | 22992 |
rs760328584 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67210112 | TGGCTCATGCCTGTA[A/T]TCCTAGCACTTGGGG | 22992 |
rs760329058 | snp | A/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67177969 | TGGGAACACTGTCAT[A/G]TATGTGCAGTTCATA | 22992 |
rs760368999 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67166511 | ATATTTCTGAGTTAT[A/G]TTATTGTTTCCAATA | 22992 |
rs760417548 | snp | A/G | 6.62548e-05 | 0.00575526 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67228158 | AGAAAGAGTCCCTCA[A/G]CATGGGTAAGTATTC | 22992 |
rs760436957 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67181594 | AAATATAGATGAACC[-/A]AAAAAAAAAAAACAA | 22992 |
rs760451691 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67225977 | GGCTGAGGCAGGAGA[A/G]TCGCTTGAACCCAGG | 22992 |
rs760458509 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67194008 | CTCACTGCACCTGTC[C/T]ACCATTTTAGATACT | 22992 |
rs760479991 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67234416 | TAGTAGAAGAGATGA[A/G]GGGAAAAGTGGTAGA | 22992 |
rs760509687 | snp | A/G | 7.75805e-05 | 0.0062277 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67231596 | GGTTGGAGTCTGGGA[A/G]TGGGGATGAGGAAGC | 22992 |
rs760511800 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255313 | CTGTGCTGTCGAGGC[A/G]CCTGCTCGCTTACTC | 22992 |
rs760550823 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67229061 | ATAAAGAATGGTCTT[C/T]GGCACAATAAAAACT | 22992 |
rs760560082 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67146436 | TTTGGCATATGGTAG[A/C]AGTTAAAACATTTAA | 22992 |
rs760584350 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67194737 | TACAAGGATAGATCC[A/C]CAACCTGCTCTTGGC | 22992 |
rs760608976 | snp | C/T | 3.52877e-05 | 0.00420031 | intron-variant | KDM2A | GRCh38.p7 | 11:67252673 | GTTAATGAAGGCGAG[C/T]TCTCTTCCCTTCTAT | 22992 |
rs760628467 | snp | A/C/G | 3.31704e-05 | 0.00407238 | intron-variant | KDM2A | GRCh38.p7 | 11:67246136 | GGAGAGCTATGAGGG[A/C/G]TTCCTGAAGTCTCAG | 22992 |
rs760638430 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67256028 | GCCAGGCTCCTCCAG[G/T]CCTCTGGTTTAGCGG | 22992 |
rs760667134 | in-del | -/ATGGTCCCTCTTCTCTCCGA | 2.86849e-05 | 0.00378704 | intron-variant | KDM2A | GRCh38.p7 | 11:67217905 | AAAATGGGAAGAGTG[-/ATGGTCCCTCTTCTCTCCGA]GGTTATTTAGCCATT | 22992 |
rs760675925 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67152522 | CCGAGGTGGGAGGAT[C/T]GCTTGAGCCTGGGAG | 22992 |
rs760681830 | in-del | -/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67234100 | CTGCAGGTGTAGTTT[-/C]ACTTAAGATCAAATA | 22992 |
rs760687327 | snp | G/T | 1.65883e-05 | 0.00287991 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67181891 | TGTCAAAATGTGTGT[G/T]GGTAAGTGTCGAGCT | 22992 |
rs760699418 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67204757 | CGACCTCCCAAAGTG[C/G]TGGGATTACAGGCGT | 22992 |
rs760708885 | snp | C/T | 4.38856e-05 | 0.00468411 | intron-variant | KDM2A | GRCh38.p7 | 11:67217928 | TAGCCATTTTTTTCC[C/T]TAATGAAAAAGAAAT | 22992 |
rs760712906 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67138965 | AGTTATTTTAAAATC[A/G]TTTCTTCATATTTCC | 22992 |
rs760718472 | snp | C/T | 3.35587e-05 | 0.00409613 | utr-variant-5-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67121272 | GGAAGAGGAAGGCAG[C/T]CCTGGAGTGGTTTCT | 22992 |
rs760763015 | in-del | -/GAG | 0.5 | 0 | cds-indel, intron-variant | KDM2A | GRCh38.p7 | 11:67250596 | GAGGGGCTGGGGGGA[-/GAG]GAGGAGGAAGAGGAG | 22992 |
rs760790573 | snp | C/G | 3.05993e-05 | 0.00391136 | intron-variant | KDM2A | GRCh38.p7 | 11:67219424 | TAATCTTATGTAACA[C/G]TTGCATGTGAAGAGG | 22992 |
rs760811222 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67165685 | AAGTGACTGCTTGCT[A/G]TCTCCCTTAATTCAC | 22992 |
rs760826515 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67242936 | ACTGAGGCAGAGTCT[A/G]GATGCTGTTCAGGGT | 22992 |
rs760839167 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67188160 | CTGTAGTCCAGCCTG[A/G]GTGACAGAGCCAAGA | 22992 |
rs760844214 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67211134 | TTGGTAGAATTCTTA[C/T]TCCCCCCATAGTATA | 22992 |
rs760844903 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67241814 | TGGCTCATGCCTGTA[A/G]TCCCAGCACTTTGGG | 22992 |
rs760847690 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67134160 | GAAACTTTGAGGAGA[C/G]AATATGAGTGGATGA | 22992 |
rs760862845 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67125122 | TGCCTCGGCCTCCCA[A/G]AGTGCTGGGATTACA | 22992 |
rs760880832 | snp | A/G | 1.69533e-05 | 0.00291142 | intron-variant | KDM2A | GRCh38.p7 | 11:67180030 | TGACCACTTGTAGGT[A/G]GGCATGAAAAAGTGC | 22992 |
rs760884256 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67127077 | GGTGGGTTGTTCTGA[A/G]GTAACAATGATTTAT | 22992 |
rs760920520 | in-del | -/GTGTGTGTGTG | | | intron-variant | KDM2A | GRCh38.p7 | 11:67152940 | TGTGTGTGTGTGTGT[-/GTGTGTGTGTG]TGTTTTCAGGAATTC | 22992 |
rs760932876 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67161696 | ACATGTGGTCTGGGG[A/T]TATACACAAGGATTC | 22992 |
rs760943999 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67140233 | TAGCTGGCTGTCATG[A/G]CGTGTACCTCTAGTC | 22992 |
rs760948745 | in-del | -/TTGT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67123995 | TGGGTTTTGTTGTTG[-/TTGT]TTGTTTGTTGGTTTG | 22992 |
rs760948992 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67216406 | GCCTTTAAGTCCTTT[A/T]TGAGGATGTAAACAG | 22992 |
rs760957268 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255401 | GGGCCCTGTGCCCCT[C/T]CTCCCCATCCATGGT | 22992 |
rs760960098 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67196916 | TTGAAAAAAAAATAG[A/T]CTCCTGGATATAGTA | 22992 |
rs760984462 | snp | C/T | 3.32635e-05 | 0.00407807 | missense, intron-variant | KDM2A | GRCh38.p7 | 11:67250518 | TCCTCTGCCAACCTT[C/T]GCCATTCCCCCCGTG | 22992 |
rs760989886 | snp | G/T | 0.000186237 | 0.009648 | missense, intron-variant | KDM2A | GRCh38.p7 | 11:67240336 | GAAACTTCACCAAGA[G/T]CCTCGGCAGCTCCAG | 22992 |
rs761008730 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67252087 | TATCCCTTTCAGTTC[C/T]GGTCTGGCCTGGCTA | 22992 |
rs761022447 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67134114 | TGGGATTTAGCTTGG[A/G]TTACCAGGAAGACTG | 22992 |
rs761041597 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67176169 | GGAAAAGATACTAGA[C/T]TTCCCTTTTGTGTTT | 22992 |
rs761042211 | in-del | -/TGTGTG | | | intron-variant | KDM2A | GRCh38.p7 | 11:67172617 | ATTAGCTCTTATAGT[-/TGTGTG]TGTGTGTGTGTGTGT | 22992 |
rs761048983 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67170516 | CTCCTGGGTTCGCAC[C/T]ATTCTCCTGCCTGAG | 22992 |
rs761073257 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67146717 | GTTTTGATGTGTTGC[A/C]CAGATTGGTCTTGAA | 22992 |
rs761073927 | snp | A/G | 1.69066e-05 | 0.00290741 | missense, nc-transcript-variant, utr-variant-5-prime | KDM2A | GRCh38.p7 | 11:67207608 | GAGACCCCAGAGGAG[A/G]AGCGAGAGAAACTCT | 22992 |
rs761076123 | snp | A/G | 1.71731e-05 | 0.00293023 | synonymous-codon, intron-variant | KDM2A | GRCh38.p7 | 11:67250646 | TGACAGTGCAGAGGA[A/G]GGGGGTGCAGCCAGG | 22992 |
rs761138261 | snp | A/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185090 | TAAAGATGCTCAGAA[A/G]ACTAAGGAATATGTG | 22992 |
rs761161786 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67236780 | AGCCAGAAAAAAGTT[A/C]GATGTTACAAATCTA | 22992 |
rs761165109 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67250972 | TAGCCTGTTGTACCC[A/G]CAGATGTCATTAGGG | 22992 |
rs761224127 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67199191 | ACTGCTTTGCCACAT[G/T]GCTATTCCCTTGTTC | 22992 |
rs761228155 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67184308 | AGATCAGCCTGGCCA[A/G]CATGGGGAAACTCCA | 22992 |
rs761253978 | snp | A/T | 1.65636e-05 | 0.00287776 | synonymous-codon, nc-transcript-variant, intron-variant | KDM2A | GRCh38.p7 | 11:67243068 | CACTGGAGTTCCTAT[A/T]GTACAGTGGCCAAAA | 22992 |
rs761274079 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67156786 | CCCAGCTACTGAGGA[C/G]GCTGAGTCAGGAGAA | 22992 |
rs761275225 | snp | A/T | 1.71734e-05 | 0.00293026 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67207489 | GCTCGATAGAGATGA[A/T]CGATGCATCTTTTAT | 22992 |
rs761316863 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67158769 | GCTCGTATTATAGGC[A/G]TGAACCACCGCCCCC | 22992 |
rs761334544 | snp | C/T | | | intron-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67120260 | TGCAAGCACGGTTTC[C/T]CTCCCGACTTCGGGC | 22992 |
rs761335060 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67171477 | TTTACTTCCAAGGGA[A/G]AGTTGAGATCTGAGA | 22992 |
rs761347077 | snp | C/G | 0.000186168 | 0.0096462 | missense, intron-variant | KDM2A | GRCh38.p7 | 11:67240254 | TAAATCCGGATTTTC[C/G]CAGAGGCAGAATATC | 22992 |
rs761365159 | snp | A/G | 1.662e-05 | 0.00288266 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67207583 | CATGGCTCAGTGGAC[A/G]CGCTACTATGAGACC | 22992 |
rs761386353 | snp | A/G | 1.65908e-05 | 0.00288012 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67253602 | CTTACTCCACCGGCT[A/G]ATAAACCAGGTATGC | 22992 |
rs761399699 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67220924 | TCCTTTTATATAGTT[C/G]ATGATCATGATTAGG | 22992 |
rs761403174 | snp | A/G | 0.000149121 | 0.00863357 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67245362 | CAAAGCCTGTGTGCA[A/G]GGAGAGTGTGGTGTT | 22992 |
rs761407685 | snp | A/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206157 | AGGTCTCAGGCAGGT[A/G]CAGTGGCTCACATGT | 22992 |
rs761426200 | snp | C/T | 5.33234e-05 | 0.00516322 | intron-variant | KDM2A | GRCh38.p7 | 11:67219413 | ACACGGGTAAGTAAT[C/T]TTATGTAACAGTTGC | 22992 |
rs761453571 | snp | C/G | 1.6585e-05 | 0.00287962 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67253461 | ATTGCAGGACTGAAA[C/G]ACCTCCTCCTAGCAG | 22992 |
rs761501820 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67121479 | GACTTTTCTGTGCAC[C/T]AGAGGAGGGGGAAAG | 22992 |
rs761503525 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67141840 | CATACACACCCTTCC[C/T]AGCCTCTGGTGTCCA | 22992 |
rs761515261 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67230527 | GCTGTTTGGGAGGCT[A/G]TTGTGGGAGGATTGC | 22992 |
rs761596505 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67157403 | TGATTGACTTTTTAA[A/G]TAGTAAACTTTATTT | 22992 |
rs761601434 | in-del | -/AGAG | | | intron-variant | KDM2A | GRCh38.p7 | 11:67157931 | CCCATCGCAAAAGAA[-/AGAG]AGAGATACATTGTTA | 22992 |
rs761603864 | snp | C/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206876 | TCTGATATAGATTTT[C/T]GTGTCCATCCTGGTG | 22992 |
rs761660633 | snp | A/G | 1.83068e-05 | 0.0030254 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67250107 | AAAATGGAAGAGAGT[A/G]ACGAAGAAGCTGTGC | 22992 |
rs761691951 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67150559 | TTGAAATGATGTTAG[A/T]TCTCTGGAAACCACT | 22992 |
rs761691984 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67166303 | GATTCTCGTGCCTCA[A/G]CCTCCCAAGTAGCTG | 22992 |
rs761697049 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67199338 | TTTAAATCAAAAGTT[-/A]AGAAATGATTAAGTT | 22992 |
rs761729892 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67202893 | CCAGCTACTCCGGAG[G/T]CTAAGGTGGAAGGAT | 22992 |
rs761732374 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67128208 | GGTTTTCACTGTGTT[G/T]TCCAGGCTGGTCTCG | 22992 |
rs761744946 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67165412 | CAGGTGTGAGCCACC[A/G]CACCCAGCTTAGAAT | 22992 |
rs761769337 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67139186 | GTTAACCAAGCCAGG[A/G]CAAGTAAGTGTACCC | 22992 |
rs761771796 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67223323 | AATTAATACAGTCTT[A/G]TAAGTTACGAGTAAA | 22992 |
rs761774949 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67240521 | GCCGTCATTGCACTT[G/T]TTCCCTCACCTGGTG | 22992 |
rs761798690 | in-del | -/GAG | | | intron-variant | KDM2A | GRCh38.p7 | 11:67196112 | TGTCGGTCATAAATT[-/GAG]GAGCAACGACATAGT | 22992 |
rs761800655 | snp | A/G | 0.000517627 | 0.0160794 | intron-variant | KDM2A | GRCh38.p7 | 11:67180260 | AGTCCTTTGATGTGG[A/G]AAGCCATAGACTCTG | 22992 |
rs761811784 | in-del | -/GGGGGGGG | 1.69223e-05 | 0.00290876 | splice-acceptor-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67207508 | GCATCTTTTATGGCA[-/GGGGGGGG]GGGAGTCGTCGCATG | 22992 |
rs761825706 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67216565 | TTTCTCTAACTTGCA[C/G]TGAATGCATTTGTAA | 22992 |
rs761830624 | snp | C/T | 3.10786e-05 | 0.00394187 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67231579 | AGATTTGGAGTTAAA[C/T]GGGTTGGAGTCTGGG | 22992 |
rs761830912 | snp | A/C/G | 0.0005295 | 0.0162638 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67252842 | CAACTGACATGGCTC[A/C/G]TCAATAGGCTGCCAG | 22992 |
rs761851429 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67152210 | TCCAGCTACTTGGGA[A/G]GCTGAGGTGGGAGGA | 22992 |
rs761864896 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255265 | CTCCTAAGGAAAAGG[C/G]AGTAGCAGATTGATC | 22992 |
rs761874658 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67180488 | TCCTCCTTCTTCTAT[C/T]CCTTGGTTTAAATTT | 22992 |
rs761893693 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67130230 | CTGGGTTGAACTCAT[A/G]CTTCGTGTTTACTCG | 22992 |
rs761922878 | snp | A/G | 1.69971e-05 | 0.00291518 | intron-variant | KDM2A | GRCh38.p7 | 11:67245500 | TTGGGGAGGGGTGGC[A/G]GTGCCAAAGGAACTG | 22992 |
rs761928384 | in-del | -/TTA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67209435 | TAGAATTTTATTTTA[-/TTA]TTATTATTATTATTA | 22992 |
rs761939128 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67190747 | GCCTAGGCAACAGAG[C/T]GAGACTCTTTAAAAA | 22992 |
rs761953385 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67149723 | CTAGGTATTAGAATC[-/T]TTTTTTTTTTTTTTT | 22992 |
rs762052401 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67241606 | AGTTTAGTGTTTGCC[A/G]AAACAGTTACCATCC | 22992 |
rs762064737 | in-del | -/GGGAGAGGAGGA | 1.71988e-05 | 0.00293243 | cds-indel, intron-variant | KDM2A | GRCh38.p7 | 11:67250592 | TGAGGAGGGGCTGGG[-/GGGAGAGGAGGA]GGAAGAGGAGGAGGA | 22992 |
rs762082758 | snp | G/T | 1.66477e-05 | 0.00288506 | intron-variant | KDM2A | GRCh38.p7 | 11:67217921 | GGTTATTTAGCCATT[G/T]TTTTCCTTAATGAAA | 22992 |
rs762096086 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67174790 | AAGTAGAATAAAGTA[A/G]TTTGTTGTTGGTTAT | 22992 |
rs762116623 | snp | A/C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67246855 | GTTTTTTTGAATACT[A/C/G]TATAGTAGCAAATCT | 22992 |
rs762151107 | snp | C/T | 3.31923e-05 | 0.0040737 | missense, intron-variant | KDM2A | GRCh38.p7 | 11:67250498 | AGCTGCAGGCCATCA[C/T]GGCCTCCTCTGCCAA | 22992 |
rs762179266 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67208957 | TTTTTTTTTTGAGGC[C/T]GAGTCTCACATTGTT | 22992 |
rs762196584 | in-del | -/TTT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67154436 | GTGTTTCTTTCTTTC[-/TTT]CTTTCTTTTTTAAGA | 22992 |
rs762218981 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67175913 | AGTTCTTCAGAGACA[C/T]ATATACAAAATAAGG | 22992 |
rs762239384 | in-del | -/AA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67241505 | AATGAAAATACATAA[-/AA]GTCCTGGTCTCCGGG | 22992 |
rs762245493 | snp | C/T | 1.7081e-05 | 0.00292237 | intron-variant | KDM2A | GRCh38.p7 | 11:67254853 | ATGTGAGCACTGTCA[C/T]TATGTCCACTTTCCC | 22992 |
rs762277489 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67195732 | GTTAGAACTTTAGTT[A/G]TATTGTACTTATATT | 22992 |
rs762295991 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67161663 | ATGCTTTAAGATGAT[C/G]TGGAAAAGTGGTTCT | 22992 |
rs762452227 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67145694 | ACCATATTCTCCCTT[C/T]CTCTTTTCTCATTAC | 22992 |
rs762506362 | snp | A/C | 0.0015655 | 0.0279338 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67207479 | GATATTAGTGGCTCG[A/C]TAGAGATGATCGATG | 22992 |
rs762535787 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67237395 | GACCCAGTATAGTTA[C/G]CTCTTATTCCATTAA | 22992 |
rs762546834 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67257700 | TGTTTTTTGTTTTTC[A/G]GAGAAATATTGTAAA | 22992 |
rs762555760 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67219166 | GATTAAGTAACTTGA[C/T]AAACCACTAAGAAGC | 22992 |
rs762568955 | snp | A/G/T | 3.33124e-05 | 0.00408109 | intron-variant | KDM2A | GRCh38.p7 | 11:67181933 | TCTTTAAGGCAAAGA[A/G/T]TTAAGACTTAGGACT | 22992 |
rs762591056 | snp | A/C | | | intron-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67120206 | TTTTTCCTCTCCGGC[A/C]CTGGCTGCTCCATGC | 22992 |
rs762602197 | snp | C/T | 3.32508e-05 | 0.00407729 | intron-variant | KDM2A | GRCh38.p7 | 11:67245958 | TCTGAGTCAGTTCTC[C/T]TGGATTCTATCTTTG | 22992 |
rs762603189 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67121571 | GTTTGGAAATGGAGT[C/T]ATATGTAGCCTTTAG | 22992 |
rs762605159 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67153865 | TGTATATCTTGCACT[G/T]ATAATCCCCTTTTTT | 22992 |
rs762622486 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67140562 | TTTGAGACCAGCCTG[A/G]CCAACATGGTGAAAC | 22992 |
rs762633036 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67228348 | TTAATGGCCAAATGA[A/G]ATACTCTGGATCTGA | 22992 |
rs762643767 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67155434 | CTGTCTCAGCCTCCT[C/G]CGTATCTGGGGCTGT | 22992 |
rs762643944 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67134024 | CAAGAAAACTGACCT[C/G]TCCTTGTTGAAGTTG | 22992 |
rs762659951 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67199830 | TAAATGAAACAGCCT[C/T]CTATTGGAAGAAGAT | 22992 |
rs762661507 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67243511 | GGACTTTGCAGTGTG[A/G]AATGGAAAAGAGAAG | 22992 |
rs762682072 | snp | C/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67205824 | TTTCTCTCCCTTCCT[C/T]GACCACCATTTTCTG | 22992 |
rs762701177 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67200523 | GCCCAGCCTGTTTGG[-/T]TTTTTTAAGACAAGG | 22992 |
rs762707934 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67205093 | ATCCAATTTCCATAG[C/T]GGCTGCACCATCTTA | 22992 |
rs762710183 | in-del | -/TGTGGA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67172647 | GTGTGTGTGTGTGTG[-/TGTGGA]TTCCTTATAGTTTTC | 22992 |
rs762729328 | in-del | -/AC | | | intron-variant | KDM2A | GRCh38.p7 | 11:67234066 | TGACGTCAGAAGACA[-/AC]AGATTTAGATTCCAG | 22992 |
rs762745393 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67138643 | AAAATTAACCAGGTG[A/T]GGTGGTGTGCACCTG | 22992 |
rs762752553 | in-del | -/TTA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67209433 | TTCTAGAATTTTATT[-/TTA]TTATTATTATTATTA | 22992 |
rs762785478 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67245124 | GTATGCTACCATGTA[A/G]TCTTCTACCCTATCC | 22992 |
rs762790514 | snp | C/T | 4.98683e-05 | 0.00499316 | intron-variant | KDM2A | GRCh38.p7 | 11:67253447 | GTCTCATTCCATCCA[C/T]TGCAGGACTGAAAGA | 22992 |
rs762840981 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67152989 | TGTTCATGGTATGTC[-/T]TTTTTTTTTTTGGAG | 22992 |
rs762846499 | snp | A/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67178860 | TGTAAACATTTGTGT[A/G]TAAGCTTTTGTTTTG | 22992 |
rs762855055 | in-del | -/AT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67124774 | TAACCCTTAACTAGC[-/AT]ATGTTTTCTTTTGTT | 22992 |
rs762860154 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67127237 | GCTGGGACTACAGGC[A/G]TGCATGTGCCACCAT | 22992 |
rs762876792 | snp | C/T | 2.16321e-05 | 0.00328871 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67181390 | GAATTCTGATGGACT[C/T]GGAATAAAGTAAGTG | 22992 |
rs762894792 | snp | A/G | 0.000169794 | 0.00921238 | intron-variant | KDM2A | GRCh38.p7 | 11:67252554 | TCTGTGAGGCAAAAA[A/G]TGATAAGGTGTGATC | 22992 |
rs762897417 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67202905 | GAGGCTAAGGTGGAA[C/G]GATTACCAGAGTCCA | 22992 |
rs762906469 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67164046 | CCCTGCCACTACTCT[A/G]TACAGCCTCTTTTTA | 22992 |
rs762920726 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67256372 | AAAAAAGAAAGAAAG[A/G]AAGGTCGGAATTTCT | 22992 |
rs762921486 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67254121 | GGGGGCCTGGCCAGC[A/C]AGTAGCTGTTGCTGC | 22992 |
rs762931066 | snp | G/T | 3.41105e-05 | 0.00412966 | intron-variant | KDM2A | GRCh38.p7 | 11:67219430 | TATGTAACAGTTGCA[G/T]GTGAAGAGGTTTACT | 22992 |
rs762936934 | snp | A/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67177432 | TTATATCCTTATTCT[A/G]TAAGCTTTTGTCTAC | 22992 |
rs762981296 | snp | C/T | 1.65987e-05 | 0.00288082 | intron-variant | KDM2A | GRCh38.p7 | 11:67243101 | GGATAAGGTAAGAAA[C/T]TATTTTCCTTGATCT | 22992 |
rs763044012 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67141605 | CCGGGAGGCAGAGCT[C/T]GCAGTGAGCTGAGAT | 22992 |
rs763061510 | snp | A/C | 0.000101654 | 0.0071286 | intron-variant | KDM2A | GRCh38.p7 | 11:67252647 | CCTGTGATGGGAGCT[A/C]CACTGATCAAGTTAA | 22992 |
rs763121543 | snp | A/C | | | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67239108 | TCATCTGGGGAATAT[A/C]AAGAATGAGACAGGC | 22992 |
rs763121863 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67199647 | TGCAGAAGAAAAGTT[C/T]AAAGCCAGGAGAGGT | 22992 |
rs763138323 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67214829 | TGAAAAGACATGATA[G/T]ACCTGGAGCTTCTTA | 22992 |
rs763178286 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67151968 | CCTGGCCTGAAATGG[C/T]ATTATTGATTACATT | 22992 |
rs763184207 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255156 | CTGAGGCCAGCGTCA[C/T]ACTCCCTCTCTGCTC | 22992 |
rs763216277 | in-del | -/A | 1.65894e-05 | 0.00288 | intron-variant | KDM2A | GRCh38.p7 | 11:67181445 | CAAAATGGCCTCGTT[-/A]ACACCCAGGGCAATA | 22992 |
rs763223464 | snp | A/G | 1.65671e-05 | 0.00287807 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67245275 | AGCTCCACGGTTAAC[A/G]CCTGTGAGGCCAGCT | 22992 |
rs763251466 | snp | A/G | 1.65696e-05 | 0.00287828 | intron-variant | KDM2A | GRCh38.p7 | 11:67215823 | GTACTTTTTTCCATC[A/G]GTACACTAATGCTGC | 22992 |
rs763277369 | snp | C/T | 7.72608e-05 | 0.00621486 | intron-variant | KDM2A | GRCh38.p7 | 11:67217895 | CTCAGGTAAGCAAAA[C/T]GGGAAGAGTGGGTTA | 22992 |
rs763295578 | snp | C/T | 3.33773e-05 | 0.00408504 | intron-variant | KDM2A | GRCh38.p7 | 11:67254447 | GTTGTTCATAATCAG[C/T]GGTGCCCCCTGCCTC | 22992 |
rs763311714 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67240471 | TGCCTGCCGGGCGAG[G/T]CCAGGACAATGCTAT | 22992 |
rs763315731 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67200960 | GCACTTTGGGAGGTC[A/G]AGGCGGGTGGATCAC | 22992 |
rs763322431 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67173216 | CAACCTCTGCCTCGC[A/G]GGTTCAAGCAATTCT | 22992 |
rs763323431 | in-del | -/AA | | | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67120034 | CTTGGACAAGAACTC[-/AA]GAGCAGAATCTCCGG | 22992 |
rs763341854 | snp | C/T | 1.88187e-05 | 0.00306741 | intron-variant | KDM2A | GRCh38.p7 | 11:67217706 | GTCAATGGCTGTTAA[C/T]AGACTAAAGTTTTTT | 22992 |
rs763357218 | snp | C/G | 3.32342e-05 | 0.00407627 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67254243 | GAACATGACCGACTT[C/G]CGGCTGGCAGGCCTT | 22992 |
rs763415497 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67210734 | TTTGTGACCTTGCTA[C/T]GTAAGTAATAACGTT | 22992 |
rs763427426 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67134143 | TGGGGGAAAGATTTT[G/T]TGAAACTTTGAGGAG | 22992 |
rs763437799 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67174418 | TTTTAAATGTCTGAC[A/G]TAGACAGTTTGAGAA | 22992 |
rs763438741 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67122059 | AGAATTCAATTTTTG[C/T]TTTTCTTAGCCAAAG | 22992 |
rs763444847 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67137211 | GAAACATAAGTGAAG[A/G]AGAGAGTTAAAATTC | 22992 |
rs763462613 | snp | A/G | 3.32701e-05 | 0.00407847 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67250344 | GCCACAGAGCGCACC[A/G]TGGTACGGGAAAAGG | 22992 |
rs763473503 | in-del | -/AA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67160819 | CTTCTCATTAATAAC[-/AA]GAGCTAGCGGGGCAC | 22992 |
rs763506075 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67247793 | AATGGTGCATATTAC[A/T]TCTATTAACATATCT | 22992 |
rs763515480 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67184188 | CAGCTGAACTGACTT[C/T]CAGGGGATTTAAAGG | 22992 |
rs763523977 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67121593 | AGCCTTTAGCTTTTA[G/T]AGAAACCATTGTATA | 22992 |
rs763551323 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67245582 | TTATACTCTCTTTTT[A/G]GCTTTATTTTGTACC | 22992 |
rs763558505 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67256461 | GAGCTTATAAATGAT[G/T]GATGCAAATTTGCAC | 22992 |
rs763582998 | snp | A/G | | | upstream-variant-2KB, synonymous-codon | KDM2A, LOC107984341 | GRCh38.p7 | 11:67117726 | TGCCAACCCCGATGT[A/G]TAACGCCCCAGCCAC | 22992 |
rs763596249 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67189950 | TAAACCTAAAGCTAA[A/C]GGAAGTAATAAAGAT | 22992 |
rs763597728 | in-del | -/TC | | | intron-variant | KDM2A | GRCh38.p7 | 11:67150207 | ATATGCATTTGTTTT[-/TC]TAGCCGATAAATAGA | 22992 |
rs763607691 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67123359 | TCAGCATGCATATAT[G/T]CCGGTGAGCCTAATT | 22992 |
rs763631387 | snp | A/G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67234532 | AACAAGTCATAGAAT[A/G/T]TAGAGTTGGAAGAGG | 22992 |
rs763637953 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67133210 | GTTCAAGCACTTCTC[C/T]TGCCTCAGCCTCCCA | 22992 |
rs763638555 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67154543 | GTTCAGGCGATTCTC[A/C]TGCCTCAGCCTCCTG | 22992 |
rs763650055 | snp | C/T | 1.73782e-05 | 0.00294767 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67207480 | ATATTAGTGGCTCGA[C/T]AGAGATGATCGATGC | 22992 |
rs763685012 | in-del | -/ATAAA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67249415 | TTGTTGCTTAGAGAC[-/ATAAA]ATAAAATGTCTCCTT | 22992 |
rs763685969 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67205094 | TCCAATTTCCATAGC[A/G]GCTGCACCATCTTAT | 22992 |
rs763725562 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67167460 | TCAGGGTAAGTGTAT[A/C]CCGACTCTTTTAGGA | 22992 |
rs763742174 | snp | C/T | | | intron-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67120217 | CGGCCCTGGCTGCTC[C/T]ATGCCCAGGCGGTCG | 22992 |
rs763786876 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67243536 | GAGAAGAAAGGGGCC[A/G]GGCATGGTGGCTCAC | 22992 |
rs763803813 | snp | C/T | 1.74986e-05 | 0.00295787 | intron-variant | KDM2A | GRCh38.p7 | 11:67252872 | GGTAAGTGAGCAGCC[C/T]TGCCGCTGTCTTTCC | 22992 |
rs763856813 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67256373 | AAAAAGAAAGAAAGA[A/T]AGGTCGGAATTTCTT | 22992 |
rs763873935 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67219201 | TCAGAGTGAAGAGTG[C/T]GATCTAGGGGTCTTG | 22992 |
rs763880528 | snp | G/T | 6.86083e-05 | 0.00585657 | intron-variant | KDM2A | GRCh38.p7 | 11:67219431 | ATGTAACAGTTGCAT[G/T]TGAAGAGGTTTACTC | 22992 |
rs763884921 | snp | A/G | 1.66776e-05 | 0.00288765 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67254911 | GACCCTGATCTACCT[A/G]CGGCGCATTGCCAAC | 22992 |
rs763890334 | snp | A/G | 3.32055e-05 | 0.00407451 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67253453 | TTCCATCCATTGCAG[A/G]ACTGAAAGACCTCCT | 22992 |
rs763941012 | snp | C/T | 3.26653e-05 | 0.00404124 | intron-variant | KDM2A | GRCh38.p7 | 11:67219247 | AGAGACTTACTGTAA[C/T]GTGTGTTTTCAGCCA | 22992 |
rs763949231 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67127363 | CTCCCAGACTCAAGC[A/G]ATCCACCTTGGCTTC | 22992 |
rs763956183 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67128184 | ATTTTTAAATTCTTT[C/T]TAGAGACAGGTTTTC | 22992 |
rs763966432 | snp | A/G | 1.69092e-05 | 0.00290763 | intron-variant | KDM2A | GRCh38.p7 | 11:67180044 | TAGGCATGAAAAAGT[A/G]CATGATTTCATCAGT | 22992 |
rs763974425 | snp | A/G | 4.82917e-05 | 0.0049136 | intron-variant | KDM2A | GRCh38.p7 | 11:67248232 | TGTTATTGTTGGATA[A/G]AGGAAGCTTGAGAGA | 22992 |
rs763978129 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67141729 | ATTGTTACTAATTAT[A/G]GTCACCCTACTTACG | 22992 |
rs763981087 | snp | C/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67179083 | TTATCTCTTTGATGA[C/T]AGCCGTTCTGGTGGG | 22992 |
rs763987464 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67164207 | AAGTGGCAGTGCCTA[A/G]ACCCAGACCTACTTC | 22992 |
rs764018392 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67191320 | GTGAGCCACTGCGCC[C/T]GACCAAGGGAACACT | 22992 |
rs764033221 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67140585 | GGTGAAACCCTGCCT[C/T]TACTAAAAATACAAA | 22992 |
rs764058096 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67214837 | CATGATAGACCTGGA[A/G]CTTCTTATTCCTAAG | 22992 |
rs764089486 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67219418 | GGTAAGTAATCTTAT[A/G]TAACAGTTGCATGTG | 22992 |
rs764134704 | in-del | -/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67132566 | TACTGGGATTATAGG[-/C]ATGAGCCGCTGCGTC | 22992 |
rs764138289 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67138667 | GCACCTGTAATCCAA[A/C]CTACTAGGGAAGCTG | 22992 |
rs764150017 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67213134 | GCTTTCTAAACACTC[C/T]CCCACAGTTAACATC | 22992 |
rs764157007 | snp | C/T | 1.65625e-05 | 0.00287766 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67245300 | CCAGCTGCTGCCTCC[C/T]CGATTGTGTCAGGAG | 22992 |
rs764234401 | snp | A/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185528 | CAGCTACTTGGGAGG[A/G]CTCAGGTAGGAGAAT | 22992 |
rs764265658 | snp | C/G | 1.65806e-05 | 0.00287924 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67254273 | TGACATCACAGATGC[C/G]ACGCTTCGCCTCATA | 22992 |
rs764270339 | in-del | -/GA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67251093 | TCTGTGATAAAACTT[-/GA]GAGTCTTGCGGGCTG | 22992 |
rs764296395 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67240494 | AATGCTATGTTACTT[C/T]GTGTTGCTTGAGCCG | 22992 |
rs764296596 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67221454 | AATGGTCTTTTATAT[A/G]TTATAGGAATGGTCA | 22992 |
rs764323271 | snp | A/G | | | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67239182 | GTATTCTGAGGGTAG[A/G]ATAATCTTACAGGCA | 22992 |
rs764327852 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67199818 | AGATTTTCCATGTAA[A/G]TGAAACAGCCTTCTA | 22992 |
rs764344410 | in-del | -/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67140301 | AGCCTGGAAGGTCAA[-/G]GCTGCAGTGAGCTTT | 22992 |
rs764349502 | snp | A/G | 1.67198e-05 | 0.0028913 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67250278 | CCCAGCGACCACCAC[A/G]GTGCCAGCCGCGATG | 22992 |
rs764362787 | snp | C/T | | | intron-variant, synonymous-codon | KDM2A | GRCh38.p7 | 11:67186574 | TATGAAGAAATATCT[C/T]GATAAAGGTAAATAC | 22992 |
rs764371939 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67173227 | TCGCGGGTTCAAGCA[A/G]TTCTCCTGCCTCAGC | 22992 |
rs764382533 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67159504 | CCAGATGATTGAGCA[C/T]TTCAAATTGTATCAG | 22992 |
rs764396001 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67135408 | GATAGGGAAATGAGA[C/T]AAAAGTTGTGGTGCT | 22992 |
rs764410330 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67137302 | AAGTTCAGCAGAGTA[A/G]TAATGCGTTTGGACC | 22992 |
rs764416773 | snp | A/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67207405 | TGTGTATTATTGAAA[A/G]TAAGAAAGGACAGTA | 22992 |
rs764483003 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67129856 | GCAGAGGTTGCTGTA[C/T]GCCGAGATCGTGCCA | 22992 |
rs764493715 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67208020 | TGGGTGACAGAACAA[C/G]ACCCTGTCTCAAAAA | 22992 |
rs764508258 | snp | A/G/T | 8.35937e-05 | 0.00646457 | intron-variant | KDM2A | GRCh38.p7 | 11:67254448 | TTGTTCATAATCAGC[A/G/T]GTGCCCCCTGCCTCC | 22992 |
rs764544381 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67123558 | CCATAAAACTCCTTT[C/T]CCAGGTAGTTATTGC | 22992 |
rs764545142 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67240777 | TTTCTTGTAGGGCCT[C/T]AGCTGGAGTCTGCCT | 22992 |
rs764581976 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67224829 | TTGGCAGCTGCAGCA[-/T]TTTTTTTTTTTTTTT | 22992 |
rs764594022 | snp | A/G | 1.66319e-05 | 0.00288369 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67250346 | CACAGAGCGCACCAT[A/G]GTACGGGAAAAGGAG | 22992 |
rs764597552 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67122079 | CTTAGCCAAAGAGAG[C/T]TTTATTAGTAGTCTC | 22992 |
rs764607220 | snp | C/T | 1.66026e-05 | 0.00288115 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67231758 | TGGCTGGGGACTCAT[C/T]TTCTGACTGTAGCCG | 22992 |
rs764686423 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67146828 | ATTGGTTATAAACTC[-/T]TAATGCCATGCTTTC | 22992 |
rs764711963 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67247987 | TTGTTGTATCTCTGT[G/T]TATTAGTTCCTGAGG | 22992 |
rs764724897 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67195496 | AAATTTTATGCCATG[A/G]GACTGTGTTCTAAAC | 22992 |
rs764735704 | in-del | -/A | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67178424 | AATAAAAAATAAAAT[-/A]AAGTGTACAATCCAG | 22992 |
rs764809838 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67203946 | GCTGGGACTATGGCC[A/G]CGTACCACCACGCCC | 22992 |
rs764813100 | in-del | -/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67161617 | TTTAAAAAATACACA[-/C]TGTTGTGACCTAAAT | 22992 |
rs764847889 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67130650 | ATTTTGGGGGGGTAA[A/C]GGACACTCTTAATTA | 22992 |
rs764868445 | in-del | -/TG | | | downstream-variant-500B | KDM2A | GRCh38.p7 | 11:67258453 | CATGTCCAGCTAATT[-/TG]TGTGTGTGTGTGTGT | 22992 |
rs764874011 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67155283 | AGGCATAAGCCACTG[C/T]GCCCCAGCCTAGCAG | 22992 |
rs764876948 | in-del | -/TCTCTC/TCTCTCTC/TCTCTCTCTC | | | intron-variant | KDM2A | GRCh38.p7 | 11:67169733 | CTCTCTCTCTCTCCT[-/TCTCTC/TCTCTCTC/TCTCTCTCTC]TCTCTCTCTCTCTCT | 22992 |
rs764878559 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67217942 | CTTAATGAAAAAGAA[A/C]TTGATGGATTACCAC | 22992 |
rs764882634 | snp | G/T | 1.66322e-05 | 0.00288371 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67231745 | CTGAAGAAAACTTTG[G/T]CTGGGGACTCATCTT | 22992 |
rs764904476 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67166223 | ACAGTCTCACTCTAT[C/T]GCCTAGGCTGGAGTG | 22992 |
rs764907434 | snp | C/T | | | upstream-variant-2KB, utr-variant-3-prime | KDM2A, LOC107984341 | GRCh38.p7 | 11:67117554 | TCCTCCTGAAAGAGT[C/T]GATGGCTGTTTATGC | 22992 |
rs764923219 | snp | C/T | 5.28174e-05 | 0.00513867 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67252847 | GACATGGCTCGTCAA[C/T]AGGCTGCCAGGTAAG | 22992 |
rs764933917 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67256140 | AGTCACCAGCCCTCT[A/G]CCTGCAGCCATGGAA | 22992 |
rs764949289 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67167369 | TATGCAGGAAGGCAG[A/G]CAACAGTGATGGGAG | 22992 |
rs764954297 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67188481 | GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 22992 |
rs764972194 | snp | G/T | 1.66123e-05 | 0.00288199 | intron-variant | KDM2A | GRCh38.p7 | 11:67181906 | GGGTAAGTGTCGAGC[G/T]TTTGGCCTCTGTCTT | 22992 |
rs764984915 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67257488 | TCTGCTCTTAGACAC[A/G]GCCTTGCCAGGAGAG | 22992 |
rs764988430 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67189851 | GTCAAAAAACAAACA[A/C]ACACCAGTCTCTTTA | 22992 |
rs765011929 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67139322 | TGATCTCAGCTCATT[A/G]CAACCTCCGCCTCCC | 22992 |
rs765021586 | snp | C/G | 1.66668e-05 | 0.00288672 | intron-variant | KDM2A | GRCh38.p7 | 11:67245944 | TGAAATGATAAAGAT[C/G]TGAGTCAGTTCTCTT | 22992 |
rs765036823 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67229557 | GCATAATTTTACTCA[C/T]AGTTTATATTCTCAG | 22992 |
rs765044939 | in-del | -/GAGGAG | | | cds-indel, intron-variant | KDM2A | GRCh38.p7 | 11:67250608 | GGAGAGGAGGAGGAA[-/GAGGAG]GAGGAGGAGGAGGAA | 22992 |
rs765065960 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67126708 | GCGAGACTCCATTTC[-/A]AAAAAAAAAAAAAAA | 22992 |
rs765071706 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67199165 | AGACTTGAAATGTTG[C/T]ATATGTTCTGACTGC | 22992 |
rs765076536 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67204934 | GTTATTTCCATCTTT[C/T]AGCTGTTTTAAATAG | 22992 |
rs765080515 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67188713 | GGAGTGTCACTTGAG[C/T]CTGGCAGGTCAAAGC | 22992 |
rs765105600 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67140511 | AATCCCAGCACTTTG[A/G]GAGGTGGAAGCGGGT | 22992 |
rs765122213 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67242034 | AGCCGAGATAGCGCC[A/G]CTGCACTCCAGCCTG | 22992 |
rs765136777 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67154434 | GGGTGTTTCTTTCTT[C/T]CTTTCTTTCTTTTTT | 22992 |
rs765152763 | snp | C/T | 1.79554e-05 | 0.00299623 | intron-variant | KDM2A | GRCh38.p7 | 11:67254473 | GCCTCCAGCCCTCCC[C/T]GGAACTTGATCAGTA | 22992 |
rs765199991 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67200348 | AGCCTCCCGAGTAGC[-/T]GGGACTACAGGCGTC | 22992 |
rs765230021 | in-del | -/TG | | | intron-variant | KDM2A | GRCh38.p7 | 11:67172621 | GCTCTTATAGTTGTG[-/TG]TGTGTGTGTGTGTGT | 22992 |
rs765242710 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67256093 | TGGCTCACTGAACTT[A/T]CAGGGCAGTCAGGGG | 22992 |
rs765257145 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67168665 | CACACACACACACAC[A/G]GTCGGGGGGATAGAC | 22992 |
rs765264323 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67251090 | TAGTCTGTGATAAAA[C/T]TTGAGAGTCTTGCGG | 22992 |
rs765282076 | snp | C/T | 3.66146e-05 | 0.00427855 | intron-variant | KDM2A | GRCh38.p7 | 11:67252669 | TCAAGTTAATGAAGG[C/T]GAGTTCTCTTCCCTT | 22992 |
rs765286331 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67227104 | CAGCTGAAATAATAA[A/T]GAAAATGCTCTTTTG | 22992 |
rs765295762 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67162366 | ACCCACTGAGATTTA[C/T]AGCAACACAGGAAAG | 22992 |
rs765300156 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67163762 | TCGGGAGGTTGCAGC[A/C]GGAGAATCGCTTGAA | 22992 |
rs765312117 | snp | C/T | 2.48555e-05 | 0.00352522 | intron-variant | KDM2A | GRCh38.p7 | 11:67252507 | TGCAAAGCGTCTAGT[C/T]GTTGTAGAGTTCAAG | 22992 |
rs765326234 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67199538 | GGTTTGGATAGAAAA[A/T]CAAACCAGCTATAAC | 22992 |
rs765328592 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67197620 | ACTTCTTCAGTGTCA[C/G]TTTATGTCTCAGAAA | 22992 |
rs765335033 | snp | A/C | 3.59958e-05 | 0.00424224 | intron-variant | KDM2A | GRCh38.p7 | 11:67180249 | TTCCAGCTTACAGTC[A/C]TTTGATGTGGGAAGC | 22992 |
rs765338197 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67127226 | CTCAGCATGTAGCTG[C/G]GACTACAGGCATGCA | 22992 |
rs765343063 | snp | A/G | 1.71953e-05 | 0.00293212 | synonymous-codon, intron-variant | KDM2A | GRCh38.p7 | 11:67250655 | AGAGGAGGGGGGTGC[A/G]GCCAGGCTGAATGGC | 22992 |
rs765365725 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67177368 | CACTTTTGTAATAAT[A/G]CTTAGCTTAAAACAC | 22992 |
rs765365788 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67216861 | CAAGGTGGAGGTTGC[A/G]GTGAGCTGAGATCGC | 22992 |
rs765444333 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67237756 | AGTTCAAGACCAGCC[C/T]GGGCAACATAGTGAG | 22992 |
rs765462803 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67252088 | ATCCCTTTCAGTTCT[A/G]GTCTGGCCTGGCTAG | 22992 |
rs765470884 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67212971 | TTGAAGGAAAGAAAG[A/G]CATCCAGGGCTTATT | 22992 |
rs765475064 | in-del | -/TC | | | intron-variant | KDM2A | GRCh38.p7 | 11:67149278 | CTTAACCTTTCTGAG[-/TC]TCAGGTTTATTCATT | 22992 |
rs765487075 | snp | C/T | 1.67624e-05 | 0.00289498 | intron-variant | KDM2A | GRCh38.p7 | 11:67242970 | TGGCTCTTTGTTCAC[C/T]CTGCCCTGATTTTTC | 22992 |
rs765513320 | snp | C/G | | | intron-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67120614 | CCTTGATTTGCACCT[C/G]TGAAATTTGTTTCAG | 22992 |
rs765553298 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67237213 | AAGAATCTTAACATT[G/T]TATTTTGGAACTATG | 22992 |
rs765567690 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67171745 | TAGGTCTCAAACTCC[G/T]GGCCTCAAGTGATCC | 22992 |
rs765571930 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67125100 | TCTGCTGACCTCGTG[A/G]TCCGCCTGCCTCGGC | 22992 |
rs765575153 | snp | A/C | 1.65721e-05 | 0.0028785 | synonymous-codon, nc-transcript-variant, intron-variant | KDM2A | GRCh38.p7 | 11:67243084 | GTACAGTGGCCAAAA[A/C]GGGATAAGGTAAGAA | 22992 |
rs765577386 | snp | G/T | 2.04895e-05 | 0.00320068 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | KDM2A | GRCh38.p7 | 11:67207673 | GCTGGAGAATATGGT[G/T]CAGAGGCCCTCCACG | 22992 |
rs765590925 | snp | C/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185411 | CCAAGGCGGGTGGAT[C/T]ACTTGAGGTCAGGAG | 22992 |
rs765640898 | snp | A/G | | | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67239065 | AGAAGGCAGTGAGGT[A/G]TCTTGACAGGATGCA | 22992 |
rs765666025 | snp | C/T | 3.31422e-05 | 0.00407063 | intron-variant | KDM2A | GRCh38.p7 | 11:67215819 | AGATGTACTTTTTTC[C/T]ATCAGTACACTAATG | 22992 |
rs765688461 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67135137 | GCAATGGCGCGATCT[C/T]GTCTCACCACAACCT | 22992 |
rs765691428 | snp | C/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206476 | GCATGGTGGCTCACG[C/T]CTGTAATCCTAGCAC | 22992 |
rs765696393 | snp | C/T | 1.66358e-05 | 0.00288402 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67254237 | GCTCCGGAACATGAC[C/T]GACTTCCGGCTGGCA | 22992 |
rs765698421 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67157812 | ATGAACCAATAATGA[C/T]TCATTATTATAAGCT | 22992 |
rs765706947 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67187597 | TTATTTATTTTGAGA[A/T]GACGTCTTGCTCTGT | 22992 |
rs765711931 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67127301 | AGGCTATCCCTGTTC[A/G]GGCTGCTCAGGCTGG | 22992 |
rs765745628 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67134183 | GTGGATGAGGCTTTA[A/G]ACAGTTGGAGATACT | 22992 |
rs765796054 | snp | C/G | 1.71926e-05 | 0.0029319 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67250148 | CCTGCGGCCCCTGCG[C/G]AGCTGCGATGAGCCT | 22992 |
rs765822163 | in-del | -/TTTC | | | intron-variant | KDM2A | GRCh38.p7 | 11:67154427 | TATTCTGGGTGTTTC[-/TTTC]TTTCTTTCTTTCTTT | 22992 |
rs765847867 | in-del | -/TTTTGTTTTG | | | intron-variant | KDM2A | GRCh38.p7 | 11:67246936 | AATGAAGAACCGGGT[-/TTTTGTTTTG]TTTTGTTTTTGAGAC | 22992 |
rs765877099 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67175867 | GTAGCATTGCTCTTG[C/T]TTTATAATGTGCTTG | 22992 |
rs765885625 | snp | A/T | 1.65647e-05 | 0.00287786 | intron-variant | KDM2A | GRCh38.p7 | 11:67228167 | CCCTCAGCATGGGTA[A/T]GTATTCTGCCTATAG | 22992 |
rs765890930 | snp | G/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67207258 | GTTAGGATTAAATGA[G/T]ACATTAGATAAAAGA | 22992 |
rs765927629 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67159372 | ATGTCCTCCTTTCTG[G/T]GTTGTCTGTTTTCTC | 22992 |
rs765928434 | in-del | -/AT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67174319 | ATTCTAGTTTTCTGG[-/AT]AACTCAGACATATTG | 22992 |
rs765969252 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67130440 | GTGAGCCACCATGCC[C/T]GGCCTTAAGCTCTCC | 22992 |
rs765992227 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67234527 | TGAAGAACAAGTCAT[A/G]GAATATAGAGTTGGA | 22992 |
rs765992301 | snp | C/G | 1.67851e-05 | 0.00289694 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67250240 | CCCGGGGTATGGTGA[C/G]TCGGTCATCCCCTGG | 22992 |
rs766082417 | snp | A/G | 4.77247e-05 | 0.00488468 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67231609 | GAATGGGGATGAGGA[A/G]GCAGTGGATCGAGAA | 22992 |
rs766085722 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67180882 | GGCCAGGCTGGTCTC[G/T]AACTCCTGACCTGAG | 22992 |
rs766133883 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67152657 | AAAAATTTAAATTAC[A/G]TATGTAGCTTACATT | 22992 |
rs766152981 | snp | C/T | 3.40327e-05 | 0.00412495 | intron-variant | KDM2A | GRCh38.p7 | 11:67181283 | TATCGTTTTTAATTA[C/T]ACCACTTATCTTTCT | 22992 |
rs766155971 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67229430 | ACATTTTTAGACTCT[C/T]ATATGTCTGAAACTG | 22992 |
rs766173604 | snp | A/G | 9.81499e-05 | 0.00700466 | intron-variant | KDM2A | GRCh38.p7 | 11:67252588 | GTACACTTGTAGAAG[A/G]ACGAGCCTCCAGGTA | 22992 |
rs766218453 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67216659 | GGCATGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 22992 |
rs766222715 | in-del | -/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67209667 | CAGGCTTGTCTCGAA[-/C]CCCTGACCTCAGGTG | 22992 |
rs766227072 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67225120 | GGTGTGAGCCATCAC[A/G]CCCGGCGGCTGCAGC | 22992 |
rs766233886 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255343 | CGCCTGCCAGGAGGC[C/T]GGGCTCTCAGTTTGG | 22992 |
rs766236220 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67131888 | TATTGTGCAGTTTGT[A/G]TGTATGTCAAGGCTT | 22992 |
rs766250847 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67201941 | GCCTGGGCATGAGAG[A/T]GAGACCCTGTCTCTA | 22992 |
rs766258864 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67166551 | GTGTATGAGGGTGGA[A/G]TGGGGGTGCTTTAAA | 22992 |
rs766294321 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67165912 | TCCATAACTTCTTAT[C/T]TGTATAATACTTTCA | 22992 |
rs766328667 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67137638 | TGAAATAGGGTACAC[C/T]GAAGGAAGAGCAGGT | 22992 |
rs766336172 | in-del | -/T | 0.00010867 | 0.00737043 | intron-variant | KDM2A | GRCh38.p7 | 11:67217919 | TGGGTTATTTAGCCA[-/T]TTTTTTCCTTAATGA | 22992 |
rs766337699 | in-del | -/AA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67252165 | CTCTGTAAGCCTGAT[-/AA]AGAGCCTCTTTTGAC | 22992 |
rs766355186 | snp | A/C | 1.65636e-05 | 0.00287776 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67245321 | GTGTCAGGAGCCAGA[A/C]GGAGACGAGTGCGAT | 22992 |
rs766380085 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67132613 | AATATAACAGTGATT[C/T]GGCCAAAGTGGCATT | 22992 |
rs766414564 | snp | A/T | 1.66952e-05 | 0.00288917 | utr-variant-5-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67121289 | CTGGAGTGGTTTCTT[A/T]ACAGTAATTTCAACA | 22992 |
rs766427768 | in-del | -/GAA | 1.72084e-05 | 0.00293325 | cds-indel, intron-variant | KDM2A | GRCh38.p7 | 11:67250605 | GGGGGAGAGGAGGAG[-/GAA]GAGGAGGAGGAGGAG | 22992 |
rs766435991 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67256031 | AGGCTCCTCCAGGCC[A/T]CTGGTTTAGCGGAGC | 22992 |
rs766481476 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67189709 | GCCAGGCATGATGGT[A/G]GACACCTGTAGTCCC | 22992 |
rs766490045 | snp | C/T | 1.672e-05 | 0.00289132 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67254885 | ACAGGTTGCAATAAA[C/T]TGACAGACCAGACCC | 22992 |
rs766493026 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67138999 | CAGTTGAATTTGCTG[A/G]CATTTTTCTAAACCA | 22992 |
rs766493543 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67251025 | CCTGCTCTATACTTT[C/G]CCATGTCTCATTGTT | 22992 |
rs766502860 | snp | C/G/T | 3.38893e-05 | 0.00411627 | intron-variant | KDM2A | GRCh38.p7 | 11:67180032 | ACCACTTGTAGGTAG[C/G/T]CATGAAAAAGTGCAT | 22992 |
rs766504048 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67247496 | ATAGTGGTGAGATTT[G/T]GGCTCACTGCAGCCT | 22992 |
rs766526463 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67226885 | TAATCTCGGCTACTG[G/T]GGAGGCTTTGGTGGG | 22992 |
rs766529642 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67196076 | CCCCATCCCAGTTAA[A/G]CTGAGTCACACGAAC | 22992 |
rs766545414 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67213090 | CCGTTGCTCCTCATC[A/T]TGTTTGTTTCTTCCA | 22992 |
rs766595141 | in-del | -/TT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67200675 | AACACACCCAGTTAA[-/TT]TTTGTGTTTTGGTAG | 22992 |
rs766648893 | snp | G/T | 8.58966e-05 | 0.00655293 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67207505 | CGATGCATCTTTTAT[G/T]GCAGGGAGTCGTCGC | 22992 |
rs766653235 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67211262 | CCCCATTTTAAGTGT[A/G]CATTTCAGTGAGTTT | 22992 |
rs766672142 | snp | A/G | 1.66341e-05 | 0.00288388 | missense, intron-variant | KDM2A | GRCh38.p7 | 11:67250519 | CCTCTGCCAACCTTC[A/G]CCATTCCCCCCGTGT | 22992 |
rs766707370 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67184337 | CATCTCTACTAAAAA[C/T]ACAAAAATTAGGCCG | 22992 |
rs766760258 | snp | A/G | 3.43206e-05 | 0.00414236 | missense, intron-variant | KDM2A | GRCh38.p7 | 11:67250647 | GACAGTGCAGAGGAG[A/G]GGGGTGCAGCCAGGC | 22992 |
rs766760360 | snp | A/G | 1.71737e-05 | 0.00293028 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67231949 | GAAGATGCTCTCATT[A/G]CTGATGTAAAGGTAA | 22992 |
rs766780639 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67148766 | AGATCATGCCATTGC[A/G]CTCCTGTCTGGGCTA | 22992 |
rs766791550 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67196979 | TCTTATTCAGTCATC[A/G]GTCTTCGGTTTTCTT | 22992 |
rs766795592 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67183231 | AAATGCTCCCCTACT[C/T]GTCACAAGACAGAAC | 22992 |
rs766810295 | snp | C/T | | | upstream-variant-2KB, synonymous-codon | KDM2A, LOC107984341 | GRCh38.p7 | 11:67117966 | TGCCCCGTCGCTGAC[C/T]CCCGCGCGAAGCTGC | 22992 |
rs766849020 | snp | A/G | 0.000193181 | 0.00982614 | intron-variant | KDM2A | GRCh38.p7 | 11:67240399 | CGGCAAACCCTTTCT[A/G]GTTTGGGGTGCGTGT | 22992 |
rs766859642 | snp | C/G | 1.65616e-05 | 0.00287759 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67253517 | CCTCAGCACCTCCAG[C/G]TGCCCCCTTCTCAGG | 22992 |
rs766882486 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67257921 | AGAGAGAGCAAGGAC[A/G]TCTTTCCTCTGACAC | 22992 |
rs766883317 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67215604 | CACAAGGAAGAGTGT[A/G]TGTGAGCATACCATA | 22992 |
rs766905020 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67191487 | GCAGCATATTAAAAG[G/T]ATTATACACCATGAC | 22992 |
rs766922545 | snp | A/C/G | 3.3065e-05 | 0.00406588 | intron-variant | KDM2A | GRCh38.p7 | 11:67219429 | TTATGTAACAGTTGC[A/C/G]TGTGAAGAGGTTTAC | 22992 |
rs766923634 | snp | C/G | 8.28343e-05 | 0.00643508 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67253478 | CCTCCTCCTAGCAGG[C/G]TGCTCCTGGTCTGCA | 22992 |
rs766973667 | in-del | -/TGTT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67151103 | ACCTTGGTAACTGTA[-/TGTT]TGACCAATTATGCTG | 22992 |
rs766987445 | snp | A/G | 1.66588e-05 | 0.00288602 | missense, nc-transcript-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67207591 | AGTGGACACGCTACT[A/G]TGAGACCCCAGAGGA | 22992 |
rs766994793 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67126975 | TTTGTATATTGATTG[C/T]CAGAACAAAGCCAGA | 22992 |
rs767027847 | snp | A/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67177570 | TTATCACTGTCTTCC[A/G]CCTCCACATCTTTTC | 22992 |
rs767073843 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67140770 | AAAAAAAAAGTTACA[A/G]GTATACTTTTGATTT | 22992 |
rs767094764 | snp | C/T | | | intron-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67120397 | ATGTAGTGACAAAAA[C/T]GGGGGGAACCTGTGT | 22992 |
rs767100530 | snp | G/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206966 | ACTAGGATAATTATC[G/T]TCATGGGCTAGGATA | 22992 |
rs767167159 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67245596 | TGGCTTTATTTTGTA[C/T]CTTTTTTCCCCAGGT | 22992 |
rs767190571 | snp | A/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206215 | GCGGGCAGATCAGCT[A/G]AGGTCAGGAGTTTGA | 22992 |
rs767190653 | in-del | -/TA | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185773 | TGGGATTGGTGCTGT[-/TA]TATAAAAGCATGAGT | 22992 |
rs767207889 | in-del | -/GTGTGTGTGT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67152910 | ACAGTGCCAGAGTGT[-/GTGTGTGTGT]GTGTGTGTGTGTGTG | 22992 |
rs767210959 | snp | C/T | 1.65605e-05 | 0.0028775 | intron-variant | KDM2A | GRCh38.p7 | 11:67248276 | ACATCTCTGTCTTCC[C/T]ATAGATGGACGGAGA | 22992 |
rs767243141 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67165446 | AACTCTTGATCTTAT[A/G]CCAGTTCCTTCTAAA | 22992 |
rs767268271 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67139481 | AACTCCTGACCTCTG[A/G]TGATTCGCCCACCTC | 22992 |
rs767298797 | snp | C/T | 5.01299e-05 | 0.00500624 | intron-variant | KDM2A | GRCh38.p7 | 11:67219453 | GGTTTACTCCAGTTA[C/T]GATAGATGTTACAAG | 22992 |
rs767301966 | snp | A/G | 1.83189e-05 | 0.0030264 | intron-variant | KDM2A | GRCh38.p7 | 11:67180263 | CCTTTGATGTGGGAA[A/G]CCATAGACTCTGAGC | 22992 |
rs767304690 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67141865 | TGTCCATCATTCTGT[A/T]CTCTGTTTATGAGAT | 22992 |
rs767319369 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67171689 | CGTCTTAATTCTCAC[A/G]GTGTGATTATCTTAG | 22992 |
rs767342456 | snp | C/T | | | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67239416 | GTAGTTGATGTTAGC[C/T]GTATTTTATTGAATA | 22992 |
rs767345174 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67232733 | ATTTATTTGAGACGG[A/C]GTCTCACTCTGTCGC | 22992 |
rs767348111 | snp | A/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67179283 | GTTTTGTTTTGTTTT[A/G]TTTTTTTGAGACGAA | 22992 |
rs767357884 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67143129 | CAGGTTCAAGTGATT[C/G]TCTTGCGTCAGCATC | 22992 |
rs767389721 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67215756 | ACTTAAGATTAAGTG[G/T]AAGATAAAGGGAGTA | 22992 |
rs767400529 | snp | A/G | 1.73866e-05 | 0.00294839 | missense, intron-variant | KDM2A | GRCh38.p7 | 11:67250675 | GGCTGAATGGCCGGG[A/G]CAGTTGGGCTCAGGA | 22992 |
rs767404589 | snp | A/G | 0.000166653 | 0.00912681 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255612 | TCTCCCAAACCTCAC[A/G]TCCTTAACTGTGCTC | 22992 |
rs767408951 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67130234 | GTTGAACTCATACTT[C/T]GTGTTTACTCGAGTC | 22992 |
rs767417269 | snp | A/G | 1.65633e-05 | 0.00287774 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67228147 | TAAGGAATTTCAGAA[A/G]GAGTCCCTCAGCATG | 22992 |
rs767460351 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67128320 | ACTGCGCCTGGACCC[G/T]TTCCCACTCTGAGGT | 22992 |
rs767474056 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67150603 | GAATATCAAGAGGAA[A/G]GGGCTGGCCATAGTT | 22992 |
rs767476172 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67166360 | CGGCTAATTTTCACA[C/T]TTTTTAGTAGAGACA | 22992 |
rs767497410 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67156249 | GCAAAACTCCGTCTC[-/A]AAAAAAAAAAAAAAT | 22992 |
rs767524303 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67200137 | AGGTTCCTTTCAAAA[C/T]GTTACTGCTCACTGG | 22992 |
rs767525906 | snp | A/C | 4.78538e-05 | 0.00489128 | intron-variant | KDM2A | GRCh38.p7 | 11:67181413 | AGTAAGTGTTTTCAG[A/C]CTGGCTGGATGTAGT | 22992 |
rs767547129 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67135876 | TCAATGGTGCACACC[C/T]TGTAGAACTATGAAC | 22992 |
rs767564435 | in-del | -/CT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67175423 | CCTAGATGACAGAGA[-/CT]CTGTCTCCGAAAAAA | 22992 |
rs767566409 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67254477 | CCAGCCCTCCCTGGA[A/G]CTTGATCAGTAAACC | 22992 |
rs767582486 | snp | G/T | 8.51825e-05 | 0.00652564 | intron-variant | KDM2A | GRCh38.p7 | 11:67245501 | TGGGGAGGGGTGGCA[G/T]TGCCAAAGGAACTGA | 22992 |
rs767583567 | in-del | -/C | 2.02669e-05 | 0.00318324 | intron-variant | KDM2A | GRCh38.p7 | 11:67215291 | TAAAATTATCTTTGA[-/C]CCCCAACCTTTCCCT | 22992 |
rs767594290 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67124727 | TCTTTTTTTCTTTAA[C/G]TTGTAAGGTGATTGG | 22992 |
rs767596724 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67191238 | CACCATGTTGGCCAG[G/T]ATGGTCTCGATCTCC | 22992 |
rs767630449 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67137407 | CTATTATATTGGTTC[A/G]GGTAAGACAATGATG | 22992 |
rs767630504 | snp | C/T | 1.75977e-05 | 0.00296624 | synonymous-codon, nc-transcript-variant, intron-variant | KDM2A | GRCh38.p7 | 11:67217748 | CTTCTGGCTCATCCC[C/T]CCTACAGCCCACAAC | 22992 |
rs767673193 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67240542 | TCACCTGGTGGGATG[G/T]GCTTTTGAATTGGGT | 22992 |
rs767673723 | snp | A/G/T | 3.32426e-05 | 0.00407681 | missense, intron-variant | KDM2A | GRCh38.p7 | 11:67250351 | AGCGCACCATGGTAC[A/G/T]GGAAAAGGAGAACAA | 22992 |
rs767683099 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67173369 | TCAGGTGATCCGCCC[A/G]CCTTGGCCTCCCAAA | 22992 |
rs767708706 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67145729 | AAATGATACCATACT[C/T]GGCTACTTTCTCTTT | 22992 |
rs767732869 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67249353 | GGTCATTTTCTTCCA[A/G]CCATAATGATAAAAA | 22992 |
rs767749045 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67159795 | TTTGAAGACAATAGT[A/G]GGAATGGATCTGTTT | 22992 |
rs767773174 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67186671 | GTTTAAGAGACGAGC[A/G]TATTTTTTAAAAGAC | 22992 |
rs767777710 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67132272 | AAGTATGGACATAGC[A/C]ATTAGAAGTTTTGTT | 22992 |
rs767807527 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67174822 | CAGGAATACAATTCC[C/T]TGTTAACCCTGGGAA | 22992 |
rs767829860 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67165365 | GACCTCAGATGATCT[A/G]CCCACCTCAGCCTCC | 22992 |
rs767829941 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67160828 | AATAACAAGAGCTAG[C/T]GGGGCACTGAGGCAT | 22992 |
rs767838367 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67195879 | TTATTTTCTATTTTA[G/T]AACCAGTTCTCAATA | 22992 |
rs767852707 | in-del | -/TTA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67237444 | TTAAATTTTTCTTTA[-/TTA]TTATTATTATTATCA | 22992 |
rs767878915 | in-del | -/TTT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67168952 | ATTTAATCCATGTAG[-/TTT]TTTTTTTTTTTTTTT | 22992 |
rs767911109 | snp | A/G | 1.65979e-05 | 0.00288074 | synonymous-codon, intron-variant | KDM2A | GRCh38.p7 | 11:67250499 | GCTGCAGGCCATCAC[A/G]GCCTCCTCTGCCAAC | 22992 |
rs767927309 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67212313 | GAAGGAATAGCATTT[A/G]TAAAAGTAGGTTCCG | 22992 |
rs767930215 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67211080 | CAAACAAACAAAAAC[A/T]TAGCTACAATCATGT | 22992 |
rs767948170 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67181210 | CAGCATAACTATATA[C/G]ACAGAATAACAAACA | 22992 |
rs767978451 | in-del | -/TCTTTTTC | | | intron-variant | KDM2A | GRCh38.p7 | 11:67163016 | AGCGTGGCCATGATT[-/TCTTTTTC]TTAAAGTTAGGAATT | 22992 |
rs767995824 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67150379 | GGGCCAAAGGAGAGG[C/T]TGGGGGAAGAGAAGA | 22992 |
rs768001013 | snp | C/T | 1.65622e-05 | 0.00287764 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67231853 | CTGACCCATTTTGAG[C/T]TTGAAGGCCTTCGCT | 22992 |
rs768038652 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67132383 | ACGCTTCCTGGGTTC[A/G]AGCGATTCTCCTGCC | 22992 |
rs768048800 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67147158 | GTTGTTGACAGTTTG[G/T]TGTAAGAGAATAGAA | 22992 |
rs768082552 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67250900 | CTGAAAGCCTGTGGG[A/G]TCTTATGAGGAGTGA | 22992 |
rs768092597 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67146659 | GACTACAGGTGCTTA[C/G]CACTACACCTGGCTA | 22992 |
rs768141016 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67134048 | GAAGTTGTACAGTGT[A/G]CTTTCTGAGGATTTT | 22992 |
rs768201365 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67149488 | TAGTTATATAGATAA[C/T]ATATATCTGTATTAT | 22992 |
rs768207500 | snp | C/T | 1.71625e-05 | 0.00292933 | synonymous-codon, intron-variant | KDM2A | GRCh38.p7 | 11:67250577 | CCCCCAGCGTGGGGA[C/T]GAGGAGGGGCTGGGG | 22992 |
rs768241136 | snp | C/G | 0.00075287 | 0.0193873 | missense, intron-variant | KDM2A | GRCh38.p7 | 11:67240228 | CTCTGGGAGATTCCA[C/G]AATATTCAAGTAAAT | 22992 |
rs768249114 | snp | A/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67121176 | TACTCCTTTCCGTGA[A/T]CAGAAAGCACAAGTT | 22992 |
rs768252885 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67236753 | AATACTTAATAAGCA[G/T]TGCATTATTACAGCC | 22992 |
rs768328843 | snp | C/T | 1.65625e-05 | 0.00287766 | synonymous-codon, nc-transcript-variant, intron-variant | KDM2A | GRCh38.p7 | 11:67243032 | GGAGGAGCTTGCCAA[C/T]AGCGATCCCAAGTTA | 22992 |
rs768329203 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67237537 | TCCTTGCCTTGAGCA[A/G]TCCTCCTGCCTCGAC | 22992 |
rs768331087 | snp | G/T | 1.65999e-05 | 0.00288091 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67207574 | TGAAATGACCATGGC[G/T]CAGTGGACACGCTAC | 22992 |
rs768341551 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67199332 | CTCTCACTTTAAATC[-/A]AAAGTTAGAAATGAT | 22992 |
rs768356843 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67172541 | GCTATTATAAATGGA[C/T]TTTTTTTCAACTTCA | 22992 |
rs768368469 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67220844 | AAAGTTGAATTTCAG[A/G]TAACTTTAACATGTC | 22992 |
rs768393453 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67171298 | GGACAGACGAGGCCG[A/G]GTCTGAAATTAGATA | 22992 |
rs768404264 | snp | A/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206830 | CTTGTGGCCTTATGC[A/G]TTTTGTTGTAGTTGT | 22992 |
rs768416905 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67122615 | GACGTGAGCCACCGC[A/G]CCTGGCCATGGCCTA | 22992 |
rs768421005 | snp | C/T | 3.90602e-05 | 0.00441912 | intron-variant | KDM2A | GRCh38.p7 | 11:67215457 | CAGAAGTAAGTGATG[C/T]GCCCTGCATCTTCCT | 22992 |
rs768473008 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67208008 | TGCATTCCAGCCTGG[A/G]TGACAGAACAAGACC | 22992 |
rs768509367 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67248505 | TTGTTTGGTTTGGTA[C/T]GTTTTTCCTTTGGTT | 22992 |
rs768529780 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67212783 | GAATGAATGCGTGGT[-/A]AAAAAAAAAAAAATA | 22992 |
rs768531245 | in-del | -/ATG | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67205962 | CAGTCTAATAAAAAT[-/ATG]ATACTTCCCTTTTGT | 22992 |
rs768541267 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67197998 | AATAAAGTAAGATAA[-/A]AAATTCCTTAAATCA | 22992 |
rs768543569 | in-del | -/AAAG | | | intron-variant | KDM2A | GRCh38.p7 | 11:67182380 | TTCAAAATTTGGGAA[-/AAAG]AAAGCAAATTAATCT | 22992 |
rs768568185 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67158706 | CTCACTATGTTACCC[A/G]GGCTGGTCTTGAACT | 22992 |
rs768569147 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67232409 | GATTCAAATTTATCT[A/G]GCATCAAGACTTAAA | 22992 |
rs768590047 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67216544 | ATTATACTCTTGTTA[C/T]TCTTTTTTCTCTAAC | 22992 |
rs768595895 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67193743 | GCAGGCGCCTCTACT[C/T]CCAACTACTTGGGAG | 22992 |
rs768596243 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67131348 | AATAATAATAACACT[A/C]TTACTCCACGGTGTG | 22992 |
rs768655731 | snp | A/G | 1.93973e-05 | 0.00311421 | intron-variant | KDM2A | GRCh38.p7 | 11:67250052 | TTTGGAAGAAAGGAA[A/G]CACTGATGTTGCTTT | 22992 |
rs768673682 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67234276 | GGACTTTCAAGTGCT[A/G]GAAAACTTGGTGCTT | 22992 |
rs768745673 | snp | C/T | 1.68323e-05 | 0.00290101 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67250205 | TTCCATGCTGCAGCT[C/T]ATCCATGACCCGGTT | 22992 |
rs768747374 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67194197 | TGTTCTCTTTGTGTA[C/T]CTCAGTTCTTGCTTC | 22992 |
rs768755482 | in-del | -/C | 1.66269e-05 | 0.00288326 | intron-variant | KDM2A | GRCh38.p7 | 11:67181919 | GCTTTTGGCCTCTGT[-/C]TTTAAGGCAAAGATT | 22992 |
rs768762187 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67174454 | CCTTTCCACTATTCT[A/G]TTTTCTGGCAGCTTT | 22992 |
rs768764124 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67208229 | AAATTTTAAAATTTA[C/T]TATTATTAAAAAAAT | 22992 |
rs768772135 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255179 | CTCTGCTCTCCTGTC[C/T]CTTGAGCCCTTCCTC | 22992 |
rs768794233 | in-del | -/AAT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67148830 | GACAGACAAAAAAGA[-/AAT]AATCCACACCCTAAA | 22992 |
rs768918466 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255791 | GCTGGAACTGTCTAC[A/C]CCAGGGACACACCCA | 22992 |
rs768945160 | snp | C/T | 1.68125e-05 | 0.00289931 | intron-variant | KDM2A | GRCh38.p7 | 11:67245485 | GCTGGGTAAAGAATT[C/T]TGGGGAGGGGTGGCA | 22992 |
rs768954255 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67202629 | TACAAAAAAAAAACT[A/G]GCCAGGCATGGTGGC | 22992 |
rs768959966 | snp | A/T | 1.94007e-05 | 0.00311448 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67219379 | TATGCAGTTAAAAAT[A/T]TACAACATTGAAGAT | 22992 |
rs768978360 | snp | G/T | 1.72442e-05 | 0.00293629 | intron-variant | KDM2A | GRCh38.p7 | 11:67254840 | GAAAGCTGTGTGTAT[G/T]TGAGCACTGTCATTA | 22992 |
rs769035071 | snp | A/G | 2.73168e-05 | 0.00369563 | intron-variant | KDM2A | GRCh38.p7 | 11:67217903 | AGCAAAATGGGAAGA[A/G]TGGGTTATTTAGCCA | 22992 |
rs769048026 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67139971 | GGCCTTCCACAGTGT[C/T]GGAACTATAGGCGTG | 22992 |
rs769051704 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67174674 | TTTATATAGTTAATT[A/G]CGACTAAACTGGGAA | 22992 |
rs769064474 | snp | C/T | 3.31565e-05 | 0.0040715 | missense, intron-variant | KDM2A | GRCh38.p7 | 11:67250468 | AAGAGCTCCACGGGA[C/T]ATCCATTGTGCCCAA | 22992 |
rs769070604 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67242743 | CTCCTGGCTCAAGTG[A/G]TCCTCCCACCTCTCA | 22992 |
rs769120628 | in-del | -/AG | | | intron-variant | KDM2A | GRCh38.p7 | 11:67183251 | CAAGACAGAACACTC[-/AG]GGGACCTCAGAAAAC | 22992 |
rs769129398 | in-del | -/AT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67129219 | GTATGTGTAGCACAC[-/AT]GTCAGACTACCACAT | 22992 |
rs769150400 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67204440 | CATATAAATGGAACT[A/G]TATAATATGTAGCCT | 22992 |
rs769238530 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67126811 | GTATGTGTAGATTTG[G/T]AATATAAGCTACACT | 22992 |
rs769251061 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67180994 | AACTCTTCAGAGACA[A/G]GGTGATGATAATTTC | 22992 |
rs769253892 | snp | A/G | 1.69086e-05 | 0.00290758 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67254946 | CCTTGATCGACCTTC[A/G]AGGATGCAAGCAGAT | 22992 |
rs769258696 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67133587 | TTTATATTTTTAGTA[C/G]AGACGGGGTTTTGCC | 22992 |
rs769264304 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67237383 | GAACTAGAAGAAGAC[C/G]CAGTATAGTTAGCTC | 22992 |
rs769266276 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67249957 | GGCCGACTCTGAGGG[A/G]ATGACCCCCTCTCCA | 22992 |
rs769286153 | snp | C/T | 1.66551e-05 | 0.00288571 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67250338 | CTGCAGGCCACAGAG[C/T]GCACCATGGTACGGG | 22992 |
rs769290359 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67146502 | ACAGATTCTCTCTCT[G/T]TGTCTGTCTTCCTTT | 22992 |
rs769292295 | snp | A/G/T | 8.64724e-05 | 0.00657496 | intron-variant | KDM2A | GRCh38.p7 | 11:67254834 | GCAGAGGAAAGCTGT[A/G/T]TGTATGTGAGCACTG | 22992 |
rs769293731 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67124473 | CCTGCCACCATGCCC[A/G]GCTAATTTTTTTGTA | 22992 |
rs769293835 | snp | C/G | 1.65946e-05 | 0.00288046 | intron-variant | KDM2A | GRCh38.p7 | 11:67121388 | CCCCCACCACACCCT[C/G]CAGTTTTAAAGTAGG | 22992 |
rs769325505 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67196665 | ACTGACATGAAGTAT[A/G]TAGAGTAACCAAAAT | 22992 |
rs769358723 | snp | C/G | 1.65625e-05 | 0.00287766 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67231809 | TGTGGGATCCCCAGT[C/G]TGCTCCCCGAAAGGA | 22992 |
rs769363707 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67212454 | TAGATTTTAAAATGG[C/T]ACAAATAATACACAT | 22992 |
rs769376129 | snp | A/G | 3.31516e-05 | 0.0040712 | missense, intron-variant | KDM2A | GRCh38.p7 | 11:67250453 | TACAGAGGCCCACCA[A/G]AGAGCTCCACGGGAC | 22992 |
rs769400536 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67133924 | GTCTCAAACTCCTGA[C/T]CTCGTGATCCTCCCA | 22992 |
rs769401216 | in-del | AGACCCCCGTCTAA/CAGAGCAAGACTCCCGTCTC | | | intron-variant | KDM2A | GRCh38.p7 | 11:67157298 | ATCCAGCCTGGGCGA[lengthTooLong]AAAAAAAAAAAAAAC | 22992 |
rs769450375 | snp | A/C/G | 0.0101094 | 0.0703752 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67207478 | GGATATTAGTGGCTC[A/C/G]ATAGAGATGATCGAT | 22992 |
rs769451571 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67148249 | CAACATTGCAAGACC[C/G]CATCTCTATTAAAAA | 22992 |
rs769453447 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67133041 | AGAGTACTTAATTGG[A/G]GATGTTGAGCCTTGA | 22992 |
rs769463629 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67141683 | AAAAAAAAAAAAAAA[-/T]TATATATATATATAT | 22992 |
rs769465973 | snp | G/T | 6.83165e-05 | 0.00584411 | missense, intron-variant | KDM2A | GRCh38.p7 | 11:67250568 | AGCCCGAACCCCCCA[G/T]CGTGGGGATGAGGAG | 22992 |
rs769467365 | snp | C/G | | | synonymous-codon, intron-variant | KDM2A | GRCh38.p7 | 11:67250565 | CCCAGCCCGAACCCC[C/G]CAGCGTGGGGATGAG | 22992 |
rs769484461 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67183800 | TGCTGCTTCTGATCA[C/G]AGAAGTACAGACAAA | 22992 |
rs769491472 | snp | A/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67184945 | AATGTCCAATTTTCA[A/G]CAAAAAATCATAAGG | 22992 |
rs769498245 | snp | A/C | 1.65877e-05 | 0.00287986 | intron-variant | KDM2A | GRCh38.p7 | 11:67121373 | GGTTAGTATTTTCTC[A/C]CCCCACCACACCCTC | 22992 |
rs769507496 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67236129 | GTCAACTGGAAGAAT[C/T]TGTGGTTTTTTTGTT | 22992 |
rs769519109 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67156457 | GGCGCGGTGGCTCTC[A/G]GCTGTAATCCCAGCA | 22992 |
rs769536508 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67219042 | GGTGCTCCAGTAAAC[A/G]TTTATTATGTGCTAA | 22992 |
rs769550194 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67154060 | AATTCCATAATGTCT[A/G]ATATTTAGAATTTTC | 22992 |
rs769554731 | snp | C/T | 0.000771903 | 0.0196305 | utr-variant-5-prime, intron-variant | KDM2A | GRCh38.p7 | 11:67240168 | TGCACGCTGCTCCCT[C/T]TGGGTAGTCTGAAGG | 22992 |
rs769561402 | in-del | -/TG | | | intron-variant | KDM2A | GRCh38.p7 | 11:67150711 | TGAGTTGGAGAAAAC[-/TG]TGGGAGAGAGGGTCA | 22992 |
rs769572465 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67123502 | TTATTTTTACATTTC[C/T]TGAATTTAACTTTTC | 22992 |
rs769590700 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67251655 | TTGGGTGGGCCCAGC[A/G]GTCTGCTTTAACAAG | 22992 |
rs769601507 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67220603 | CTAGGATGATACACA[A/G]CTAATACCCTTCTAG | 22992 |
rs769615374 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67209906 | TCTCTACAAAATTTG[A/G]AAACTTAGCCAGGCA | 22992 |
rs769673445 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67191227 | AGATGGGGTTTCACC[A/G]TGTTGGCCAGGATGG | 22992 |
rs769674455 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67236134 | CTGGAAGAATTTGTG[G/T]TTTTTTTGTTTTTTG | 22992 |
rs769724029 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67125970 | AAAAAAAAAGGCCAG[A/G]CACAGTGTCTCACGC | 22992 |
rs769737980 | snp | G/T | 3.6293e-05 | 0.00425972 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67231570 | CATATTGGTAGATTT[G/T]GAGTTAAATGGGTTG | 22992 |
rs769751847 | snp | C/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67178661 | GTCTTTTATGACTGG[C/T]TTTTTTTTTATTTGG | 22992 |
rs769753950 | snp | A/G | 0.000487686 | 0.0156079 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255566 | CCCCAGGAGTCCCAG[A/G]CCCGTGCCGATCACA | 22992 |
rs769811558 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67246382 | GACTCTGGATTGGGT[A/G]TGTAGAGTTCCCAGG | 22992 |
rs769839540 | snp | A/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67121065 | AATGTGATTAATGTT[A/G]AACATGACATGGAAC | 22992 |
rs769845429 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67174214 | AGTAAGCTGAGATTG[C/T]GCCACTGCACTCCAG | 22992 |
rs769867640 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67192328 | CTGCAACTTGCTTTT[C/T]CACTAAACATTGCAT | 22992 |
rs769889928 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67202711 | AACCCAGGAGGCGGA[A/G]CTTGCAGTGAGCCGA | 22992 |
rs769900903 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67127834 | TGCTTCAGCCTCTGA[A/G]TAGCTGGGATTACAG | 22992 |
rs769938585 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67164983 | GATGAAGACATAGTT[G/T]TCTCTGCTTTAACTT | 22992 |
rs770024463 | snp | G/T | 1.66352e-05 | 0.00288398 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67252792 | AGAGGCAGCCAGTCA[G/T]CCTTGACCTCAGTTG | 22992 |
rs770058800 | in-del | -/GC | | | intron-variant | KDM2A | GRCh38.p7 | 11:67253979 | AGCCTTTTGCTGTGT[-/GC]ATGAGGCATAATCTA | 22992 |
rs770062376 | snp | G/T | 3.32331e-05 | 0.0040762 | intron-variant | KDM2A | GRCh38.p7 | 11:67181834 | ATATACTTACTGGTG[G/T]TTGTTTCATAGAATG | 22992 |
rs770072641 | in-del | -/TTTC | | | intron-variant | KDM2A | GRCh38.p7 | 11:67142027 | TATGGATGAATGGTA[-/TTTC]TTTCATTCATTCATT | 22992 |
rs770078713 | snp | C/T | 3.55347e-05 | 0.00421498 | intron-variant | KDM2A | GRCh38.p7 | 11:67252633 | GAAGCCATAAGCAGC[C/T]TGTGATGGGAGCTCC | 22992 |
rs770083425 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67215620 | TGTGAGCATACCATA[A/G]CACACAACCACACAG | 22992 |
rs770096959 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67179858 | CAAAGAATTAGCAAG[A/G]GTAAAATTCATAGAG | 22992 |
rs770099205 | in-del | -/ATA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67222019 | AAAGAAAAAAAATGT[-/ATA]ATTCCATAGTAAAAT | 22992 |
rs770113717 | in-del | -/AAA/AAAA/AAAAA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67155937 | ATTTTTTAAACGGCT[-/AAA/AAAA/AAAAA]AAAAAAAAAAAAAAA | 22992 |
rs770162489 | snp | C/T | 1.65792e-05 | 0.00287912 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67245246 | CCCATTACGAAGCCT[C/T]ACACTATGAAACCAG | 22992 |
rs770163982 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67187601 | TTATTTTGAGATGAC[A/G]TCTTGCTCTGTTGCC | 22992 |
rs770171032 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67232281 | ATTAAACTTAAGTTA[A/C]CTTGAGATAAAACTC | 22992 |
rs770174728 | snp | A/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67186387 | AAAACAAAACTGTCA[A/G]CCAAGCATCCTATAT | 22992 |
rs770179866 | in-del | -/AT | 1.83694e-05 | 0.00303057 | intron-variant | KDM2A | GRCh38.p7 | 11:67180265 | TTGATGTGGGAAGCC[-/AT]ATAGACTCTGAGCAT | 22992 |
rs770228966 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67240901 | CCAGTAACTGAGTCT[C/T]GTATGTGTGAACAGC | 22992 |
rs770242016 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67165966 | AAATTGGCATGACCA[A/G]TACCATGTATTATAC | 22992 |
rs770262466 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67200585 | GGTACAATCATGGCT[C/T]ACTGCAGGCTCAGTG | 22992 |
rs770269744 | in-del | -/CTTAAATTCCCCACTCGGCCAAAGGTGCGGGTTCCTACCATCCC | 1.66866e-05 | 0.00288842 | frameshift-variant, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67245456 | TCCGACAGTGCTTGG[lengthTooLong]CAGTGAGTGATCTGC | 22992 |
rs770311318 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67168954 | TTAATCCATGTAGTT[-/T]TTTTTTTTTTTTTTT | 22992 |
rs770314957 | in-del | -/TTG | | | intron-variant | KDM2A | GRCh38.p7 | 11:67235320 | TTTTTTTTTTTTTTT[-/TTG]TGAGACTGAGTTTCA | 22992 |
rs770316780 | snp | C/G | 0.00304784 | 0.0389183 | utr-variant-5-prime, intron-variant | KDM2A | GRCh38.p7 | 11:67240206 | CTGGACTGCCCTGCC[C/G]TATGTGCTCTGGGAG | 22992 |
rs770327961 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67129457 | AGCCGGGCATAGGCC[A/G]GGCGCGGTGGCTCAC | 22992 |
rs770330568 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67150210 | TGCATTTGTTTTTCT[A/G]GCCGATAAATAGATC | 22992 |
rs770337194 | snp | C/T | 1.66299e-05 | 0.00288352 | intron-variant | KDM2A | GRCh38.p7 | 11:67254438 | GCCGCTACAGTTGTT[C/T]ATAATCAGCGGTGCC | 22992 |
rs770340496 | snp | C/G | 1.91507e-05 | 0.00309434 | intron-variant | KDM2A | GRCh38.p7 | 11:67217685 | TGAGGGAGACGACTG[C/G]GTCATGTCAATGGCT | 22992 |
rs770351120 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67216456 | ATTCATTCAGTTATA[G/T]TCCAGCTTGTGAAAA | 22992 |
rs770361481 | in-del | -/CTTC | | | intron-variant | KDM2A | GRCh38.p7 | 11:67146510 | TCTCTCTTTGTCTGT[-/CTTC]CTTTTTATTGTTTGA | 22992 |
rs770381807 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67138180 | AAGTCTGTATTTGAC[C/T]GTGAGTCTCTTTTTA | 22992 |
rs770412606 | snp | C/T | 1.67016e-05 | 0.00288973 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67254223 | GACAATCGCAGCAAG[C/T]TCCGGAACATGACCG | 22992 |
rs770416187 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67164453 | ATAACTGTTCATTAA[G/T]TGTTGATCTTGCTAT | 22992 |
rs770425229 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67175591 | GTATCCTTACATTCT[C/T]CCTATTGAAGGTGTA | 22992 |
rs770426802 | snp | C/T | 4.53391e-05 | 0.00476104 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | KDM2A | GRCh38.p7 | 11:67217880 | TACCTTCGTCATTCC[C/T]TCAGGTAAGCAAAAT | 22992 |
rs770434838 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67137040 | CTTTGAAGTTGAGAC[C/T]TAAAGGGTGACTAGG | 22992 |
rs770443513 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67173893 | ACAATTTTTTTTTTT[A/T]ATAAGATAGGGTCTT | 22992 |
rs770444655 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67210132 | AGCACTTGGGGAGGC[C/T]GAAGGCAGACAGATT | 22992 |
rs770448728 | snp | A/G | 3.31439e-05 | 0.00407073 | intron-variant | KDM2A | GRCh38.p7 | 11:67215995 | TCTGAAGTTGGTTGT[A/G]TGACTTTGCTTCAGT | 22992 |
rs770469521 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67160343 | CGGTTTAGGAAGAGA[C/T]TATAGCTTGAACCAT | 22992 |
rs770493674 | in-del | -/AA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67148462 | TTTTTCATGGGGTAA[-/AA]CTCAAATAATAGGTA | 22992 |
rs770500474 | snp | C/T | 1.65888e-05 | 0.00287996 | intron-variant | KDM2A | GRCh38.p7 | 11:67254424 | AATATGGCAGGTATG[C/T]CGCTACAGTTGTTCA | 22992 |
rs770515720 | snp | A/G | 1.66768e-05 | 0.00288758 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67250332 | CTGCGGCTGCAGGCC[A/G]CAGAGCGCACCATGG | 22992 |
rs770541961 | snp | A/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67178197 | GATCGCTTGAGCACA[A/G]GAGTTCGAGACCAGC | 22992 |
rs770560600 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67183204 | GTGCTCAGTAAATCC[A/G]TTGAATAATGAAAAT | 22992 |
rs770590643 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67161451 | TTAGTATGTTGTAGT[A/G]CAGTGTTTTGCACAG | 22992 |
rs770601766 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67180881 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTGA | 22992 |
rs770605210 | snp | A/G | 5.03208e-05 | 0.00501576 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67231716 | TGGGCAAAACCTGCC[A/G]AAGTCTTCCAAGTCT | 22992 |
rs770606757 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67214602 | CCTTGGCCTCCCAAA[C/G]TGTTGGGGATTACAG | 22992 |
rs770634702 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67145353 | AAATTAGCCAGGTGT[A/G]GTTGCGTGTGCCTGT | 22992 |
rs770651000 | in-del | -/A | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67184870 | ACAATAATAAAACAC[-/A]AAAAAACCCTGGGGA | 22992 |
rs770670883 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67146387 | CCTGAGGGCAAAAAT[C/G]ATGGCAGTCTTATTT | 22992 |
rs770691623 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67149777 | CTAGGCTGGAGTGCG[A/C]TGATACGATCTCGGC | 22992 |
rs770724394 | snp | A/T | 1.65756e-05 | 0.00287881 | missense, intron-variant | KDM2A | GRCh38.p7 | 11:67250426 | TCCGGGGATCGTACC[A/T]CACTGTCACGCTACA | 22992 |
rs770795441 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67152481 | GGCATGGTGGTGCAC[A/C]TCTGTAGTCCTTGCT | 22992 |
rs770805272 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67204758 | GACCTCCCAAAGTGC[C/T]GGGATTACAGGCGTG | 22992 |
rs770832238 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67249347 | AAAGGTGGTCATTTT[C/T]TTCCAACCATAATGA | 22992 |
rs770857787 | snp | A/T | 0.00012608 | 0.00793876 | intron-variant | KDM2A | GRCh38.p7 | 11:67196404 | TTTAACCTCTTGCAT[A/T]GCTGGGACTGCAAGC | 22992 |
rs770857926 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67182631 | TCCGCCTGCTGCATT[C/T]GAGCAGTTCTCCCAC | 22992 |
rs770874733 | in-del | -/AA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67240452 | GTGAAGAGGCAGGAG[-/AA]ACTGCCTGCCGGGCG | 22992 |
rs770883219 | snp | A/C | 1.6764e-05 | 0.00289512 | intron-variant | KDM2A | GRCh38.p7 | 11:67248416 | ACAGAAAGGAGGCAT[A/C]AAATGTGGGGGATTG | 22992 |
rs770898166 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67257284 | CATTTTTACCGTGCA[C/T]GTAAATTGGTCAGCA | 22992 |
rs770899792 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67190772 | TAAAAAAAAAAATAC[C/T]ACGAACAATTGTTCA | 22992 |
rs770940627 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67171070 | TACATGCATAGTGCT[C/T]GTTACAGTACCTGGC | 22992 |
rs770974719 | in-del | -/ATC | | | intron-variant | KDM2A | GRCh38.p7 | 11:67140377 | TCTCAAAAAAAAAAT[-/ATC]ATGGTTTTATACAAA | 22992 |
rs770982048 | in-del | -/CACACACACACACAC | | | intron-variant | KDM2A | GRCh38.p7 | 11:67168584 | CTTGTATGAATTATA[-/CACACACACACACAC]ACACACACACACACA | 22992 |
rs770993241 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67140290 | AGGATCACTTGAGCC[C/T]GGAAGGTCAAGGCTG | 22992 |
rs770994592 | snp | A/G | | | upstream-variant-2KB, utr-variant-3-prime | KDM2A, LOC107984341 | GRCh38.p7 | 11:67117491 | TACCTTGGAGTTCAA[A/G]CCTTGATAGAATTAG | 22992 |
rs770994964 | snp | C/G | 3.48347e-05 | 0.00417326 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67207464 | CTTACTATATTTAAG[C/G]ATATTAGTGGCTCGA | 22992 |
rs770998012 | in-del | -/GGGGTTGGGGTTGGGGTT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67142558 | GGTGAAGTTGGCCGG[-/GGGGTTGGGGTTGGGGTT]GGGGTTGGGGTTGGG | 22992 |
rs771014343 | snp | A/C | 0.000943205 | 0.0216959 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255006 | CAGACTTGTCCATCA[A/C]CAGCCTCTACTGCCT | 22992 |
rs771050802 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67171416 | ATGTGAGTTGGATTC[-/A]GAGTGTAGAAGACTT | 22992 |
rs771052743 | snp | C/T | 1.65608e-05 | 0.00287752 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67228114 | TGTGTACTGCATAAC[C/T]AACCGTTCCCACCTA | 22992 |
rs771064858 | in-del | -/G | | | upstream-variant-2KB, utr-variant-3-prime | KDM2A, LOC107984341 | GRCh38.p7 | 11:67117270 | TTTCAGTCGGCTGTT[-/G]GGAGTAATTATGCAA | 22992 |
rs771092073 | snp | C/T | 1.65608e-05 | 0.00287752 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67228088 | ATGTGTTGGTATGTG[C/T]TGGAGCGCTATGTGT | 22992 |
rs771146329 | snp | A/C | 1.73087e-05 | 0.00294177 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67180213 | TACTTTTATGGAAGG[A/C]AAAGGTCAGTATTGT | 22992 |
rs771146505 | snp | A/G | 5.94972e-05 | 0.00545391 | intron-variant | KDM2A | GRCh38.p7 | 11:67231531 | CACATGGCAGAGTGA[A/G]ATGTTCTTACTGCAT | 22992 |
rs771152935 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67127103 | TTTATTTCTGTATTT[A/C]TTTTTCTTTTTGGAG | 22992 |
rs771154888 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67141195 | TTCTGTCCCTTATTA[C/T]TTAACCATTTCTTCA | 22992 |
rs771177716 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67215507 | AAAGCAATAGCAAGG[A/G]TTGGCTTCTCCCTTA | 22992 |
rs771232627 | snp | C/T | 2.30513e-05 | 0.00339487 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67181321 | TCCTATGGTGACAGA[C/T]TTTAATGTAGAGTAT | 22992 |
rs771302219 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67200367 | ACTACAGGCGTCCGC[C/T]ACCACGTCCGGCTAA | 22992 |
rs771304801 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67199332 | CTCTCACTTTAAATC[A/G]AAAGTTAGAAATGAT | 22992 |
rs771344024 | snp | C/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67178334 | CACCTGAGCCTAGGA[C/G]GTTGAGGTTGCAGTG | 22992 |
rs771365250 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67254771 | TTGTGGGACAAAGAG[C/G]GCTTTTGTTTAGCAT | 22992 |
rs771366038 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67253824 | AAGTCCATTTTGTGA[C/G]TTGGTGGAGTTTGGG | 22992 |
rs771413718 | snp | C/T | 1.83192e-05 | 0.00302643 | missense, intron-variant | KDM2A | GRCh38.p7 | 11:67250786 | TGCGAGTGTGCAAGA[C/T]GTGGTATAAATGGTG | 22992 |
rs771469836 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67121592 | TAGCCTTTAGCTTTT[A/G]TAGAAACCATTGTAT | 22992 |
rs771475257 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67163488 | GCAAGTATGACTTAT[A/C]TCTAGCCACTTAGGC | 22992 |
rs771491306 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67232050 | ATATAGGAATTTTGG[A/G]TGATCTCTGGTTCAG | 22992 |
rs771503812 | snp | C/G | 1.65638e-05 | 0.00287778 | missense, nc-transcript-variant, intron-variant | KDM2A | GRCh38.p7 | 11:67243072 | GGAGTTCCTATAGTA[C/G]AGTGGCCAAAAAGGG | 22992 |
rs771510096 | snp | A/G | 6.37206e-05 | 0.00564414 | intron-variant | KDM2A | GRCh38.p7 | 11:67252608 | GCCTCCAGGTACTCT[A/G]CTTTTCCCAGAAGCC | 22992 |
rs771521101 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67134988 | ACTCCTTTTAACATA[C/T]GCAAAGATCAACTTA | 22992 |
rs771528849 | in-del | -/GTCCAGGACAATGCTAT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67240470 | CTGCCTGCCGGGCGA[-/GTCCAGGACAATGCTAT]GTTACTTCGTGTTGC | 22992 |
rs771556624 | in-del | -/C | 1.65905e-05 | 0.0028801 | intron-variant | KDM2A | GRCh38.p7 | 11:67121371 | TGGTTAGTATTTTCT[-/C]CCCCCCACCACACCC | 22992 |
rs771559679 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67187068 | ATAGTAGTGAAGTCA[A/G]ACTGGTATTAATTAA | 22992 |
rs771561726 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67172718 | GTTTTACTTGTTCCT[C/T]TCCAAACTTTTCTTT | 22992 |
rs771581906 | snp | C/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67186300 | CAGTAAAATTATGAA[C/T]GAATTTCTCATCAGA | 22992 |
rs771584758 | snp | C/G | 1.65627e-05 | 0.00287769 | missense, nc-transcript-variant, intron-variant | KDM2A | GRCh38.p7 | 11:67243049 | GCGATCCCAAGTTAG[C/G]CCTCACTGGAGTTCC | 22992 |
rs771585444 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67150055 | TACTCAGTAAACAAA[A/C]GATAGCAAAATTCAA | 22992 |
rs771591882 | snp | C/T | 3.31835e-05 | 0.00407316 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67245233 | GGTTCCTACCATCCC[C/T]ATTACGAAGCCTCAC | 22992 |
rs771597482 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67136610 | TGAGATTGAGTGATC[A/C]GTGAAAGGCTTCTTG | 22992 |
rs771602027 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67225064 | AACTCTTGACCTCAG[A/G]TGATCCACTTGCCTT | 22992 |
rs771670155 | snp | A/G | 6.78415e-05 | 0.00582376 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67254207 | TGCCTGTACAGGTCA[A/G]GACAATCGCAGCAAG | 22992 |
rs771670972 | snp | C/T | 1.97834e-05 | 0.00314504 | intron-variant | KDM2A | GRCh38.p7 | 11:67215460 | AAGTAAGTGATGCGC[C/T]CTGCATCTTCCTCCG | 22992 |
rs771673070 | snp | A/G | | | utr-variant-5-prime, intron-variant | KDM2A | GRCh38.p7 | 11:67240137 | GCTGAAGGGCTCGAG[A/G]AGGAGCCCAGAGCGC | 22992 |
rs771704707 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67247329 | TCCTAACCTCAAGTG[A/G]TTCACCCGCCTTGGC | 22992 |
rs771755826 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67173817 | TCCTGAGCTCAAACA[A/C]TCCTGCTGTCCCAGT | 22992 |
rs771756375 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67144937 | TGCCAGTGGCGCAAT[C/T]TCAGCTAACTGCCGA | 22992 |
rs771758859 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67123067 | CCTCAAATTCCTGGG[A/C]TCAAGCAATCTTCCA | 22992 |
rs771761236 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67246574 | GAGCTAAATAGCTTT[-/A]AAAAAAAAAAGTAAT | 22992 |
rs771768404 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67193895 | ACGTATTTATTGAGA[C/T]AGGGGTCTCGCTGTG | 22992 |
rs771798119 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67208128 | ACAAGACTATTTGAC[A/G]AGAATAATTTGTATT | 22992 |
rs771807475 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67160271 | GGATCATTATTGATG[A/T]CTCTGGGTATGCTGT | 22992 |
rs771834320 | snp | G/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67177741 | TGCATGCTAAAATAA[G/T]GATCAAGCACAGAAT | 22992 |
rs771840445 | in-del | -/TT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67242566 | TATGAGAAGTAACAC[-/TT]GTCACCACAGTAAGT | 22992 |
rs771873470 | in-del | -/AA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67197997 | ACAATAAAGTAAGAT[-/AA]AAATTCCTTAAATCA | 22992 |
rs771895529 | snp | A/G | 6.62537e-05 | 0.00575521 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67254392 | GGTCTTCCACTCGCT[A/G]CTCTCTCACAGAGCT | 22992 |
rs771906931 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67248612 | CAAATTCCTAAGGTC[C/T]TTTTATACTCTGGGG | 22992 |
rs771929929 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67180510 | TTTAAATTTAATTAA[A/G]AATAGTACAATAGAA | 22992 |
rs771941810 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67235866 | CTTGCGATCCACCTG[C/T]CTTGGCCTCCCAAAG | 22992 |
rs771947236 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67231479 | TGTCATTTATAGCCT[C/T]AAGGCCCCTATCATG | 22992 |
rs771975877 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67194801 | CCTACTTTGATTCAC[C/T]TGCTGTTGCAGCAGG | 22992 |
rs771990150 | snp | C/T | 3.36095e-05 | 0.00409922 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67250224 | CATGACCCGGTTTCC[C/T]CCCGGGGTATGGTGA | 22992 |
rs771992532 | in-del | -/AT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67148082 | TAAAGTATTTACTAG[-/AT]CGCTGATTTGTTACA | 22992 |
rs772019798 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67204622 | TCAGTCTCCCGAGTA[C/G]CTGGGACTACAGGTG | 22992 |
rs772031865 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67250020 | GCAAGGGAGGTCCAC[C/T]CTGTCGGTTCAGAGG | 22992 |
rs772038098 | snp | A/G | 1.67421e-05 | 0.00289323 | intron-variant | KDM2A | GRCh38.p7 | 11:67253422 | GCTGGGAAACAGTGT[A/G]TTATTACATGTCTCA | 22992 |
rs772056999 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67146234 | TCCTGACCTCCTGAT[C/G]TGCCTGCCTCAGCCT | 22992 |
rs772080094 | snp | A/G | 1.67097e-05 | 0.00289043 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67250321 | GGCGGCAGTTGCTGC[A/G]GCTGCAGGCCACAGA | 22992 |
rs772099244 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67194406 | GGCGTAGGTCCTCCT[A/G]TGTCAATGGCACATC | 22992 |
rs772107830 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67217459 | GGGACTGCCTAGGTA[A/G]TGAGCTGAATGGTCC | 22992 |
rs772139775 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67153963 | ACATCATGACACATT[A/T]TTCCTAAATGTTTTA | 22992 |
rs772140864 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67232623 | TATTTCTCCTAATGC[G/T]ATCCCTCCTCCAGCT | 22992 |
rs772171917 | snp | C/T | 1.87461e-05 | 0.00306148 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67231650 | TGAGCAGCAGGCGTT[C/T]TGTCCTCACTAGCCC | 22992 |
rs772201786 | snp | A/C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67241788 | AAACGAAAAGATTTG[A/C/G]CCAGGTGCAGTGGCT | 22992 |
rs772227964 | snp | A/T | 1.65792e-05 | 0.00287912 | intron-variant | KDM2A | GRCh38.p7 | 11:67246130 | AGGTGAGGAGAGCTA[A/T]GAGGGGTTCCTGAAG | 22992 |
rs772244184 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67140120 | AATCCCAACACTTTG[A/G]GAGGCTAAGGCAGGA | 22992 |
rs772267534 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67242875 | GTCTCTATATGAAGG[G/T]CAAATACAGACAGTT | 22992 |
rs772271067 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67133855 | TGCGCCACCACACCC[A/G]GGTAATTTTTGTATT | 22992 |
rs772296448 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67205471 | TGTTTGTTCGTCTTA[C/T]AAGGAAGACAATAGA | 22992 |
rs772297490 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67154956 | CTACCTTTTAGCTAC[C/T]GTGAATAGTGCTGCT | 22992 |
rs772297693 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67229731 | AGAAATTAGCCAGGC[A/G]TGGTGTTGCGCACCT | 22992 |
rs772315176 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255936 | CTTTCCCAGGATGCA[C/T]GTCCTCAGAGGGAGC | 22992 |
rs772315732 | snp | A/C/T | 7.73283e-05 | 0.00621766 | intron-variant | KDM2A | GRCh38.p7 | 11:67248383 | CAGGTAAAGGAACCT[A/C/T]ATCAGATTTGCACTG | 22992 |
rs772327544 | in-del | -/AGAGGAGGAGGA | 0.000137649 | 0.0082949 | cds-indel, intron-variant | KDM2A | GRCh38.p7 | 11:67250595 | GGAGGGGCTGGGGGG[-/AGAGGAGGAGGA]AGAGGAGGAGGAGGA | 22992 |
rs772332007 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67198130 | GTCTCAGGAGTGGCA[A/G]GGATGGAAGAAAATT | 22992 |
rs772368779 | in-del | -/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67170383 | TATCCTACCAAGCAT[-/G]GGGGTTTTTTTTTTT | 22992 |
rs772384088 | snp | A/G | 1.66654e-05 | 0.00288659 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67180151 | GGAAAAAGAACTTTT[A/G]ACTTGGAAGAGAAAC | 22992 |
rs772398828 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67212635 | TCCCAAGGCTAAAGA[G/T]TAACCTAAGAAGAAA | 22992 |
rs772461019 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67127574 | TATGAAATAGCTAAA[C/T]CATTTATCTGTTACA | 22992 |
rs772461816 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67126963 | AATATTAGTACTTTT[A/G]TATATTGATTGCCAG | 22992 |
rs772480573 | snp | C/G | 0.000185925 | 0.00963993 | missense, intron-variant | KDM2A | GRCh38.p7 | 11:67240269 | CCAGAGGCAGAATAT[C/G]TAACTCCTTCAGGAG | 22992 |
rs772526286 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255218 | GGGCAGAGAGGGTGG[-/T]GGACACCAGGCTTAT | 22992 |
rs772541060 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67227813 | TGACCTCAAGTGATC[C/T]ACCCGTCTGGGCCTC | 22992 |
rs772550723 | snp | C/T | 3.51945e-05 | 0.00419476 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67254977 | CACTCGAAAAGCCTG[C/T]GAGCACTTCATCTCA | 22992 |
rs772554572 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67223895 | ATACCTATTGGTTGT[C/T]GTCTCTCTCCTCTGT | 22992 |
rs772575125 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67190622 | AAAACTGAGCTGGAC[A/G]TGGTTGCATGTTCCT | 22992 |
rs772577130 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67175916 | TCTTCAGAGACACAT[A/T]TACAAAATAAGGTGA | 22992 |
rs772613420 | snp | C/T | 2.07738e-05 | 0.00322281 | intron-variant | KDM2A | GRCh38.p7 | 11:67215473 | GCCCTGCATCTTCCT[C/T]CGTGTGCTGTGGGAG | 22992 |
rs772619697 | snp | C/T | 4.98128e-05 | 0.00499038 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67253609 | CACCGGCTGATAAAC[C/T]AGGTATGCTCTGGAC | 22992 |
rs772620721 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67184359 | ATTAGGCCGGGTGCG[G/T]TGGTTGACGCCTGTA | 22992 |
rs772638468 | snp | A/T | 2.80966e-05 | 0.003748 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255079 | CAGCCCAGATTCAAC[A/T]GGAAACCGATCTTCC | 22992 |
rs772640142 | in-del | -/TGT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67137999 | GACGGGGTTTCACCA[-/TGT]TGGCCAGGATAATCT | 22992 |
rs772655949 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67123996 | GGTTTTGTTGTTGTT[-/T]GTTTGTTTGTTGGTT | 22992 |
rs772684146 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67217937 | TTTTCCTTAATGAAA[A/G]AGAAATTGATGGATT | 22992 |
rs772685098 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67209610 | ACCACACCCGGCTAA[-/T]TTTTTGTATTTTTAG | 22992 |
rs772701870 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67221426 | TTAATGAAGAATTCA[A/C]AACTTTTATATGAAT | 22992 |
rs772724032 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67143686 | CTCCCAGGCTGGAGT[A/G]CAATGACGCGATCTT | 22992 |
rs772747997 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67240474 | CTGCCGGGCGAGTCC[A/G]GGACAATGCTATGTT | 22992 |
rs772762421 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67172730 | CCTTTCCAAACTTTT[A/C]TTTTTCTTGCCTAAT | 22992 |
rs772776309 | snp | C/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206965 | AACTAGGATAATTAT[C/T]TTCATGGGCTAGGAT | 22992 |
rs772786194 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67160093 | CCTGCCTCACTGCCT[C/T]TTCCCTGATAATTTT | 22992 |
rs772865147 | in-del | -/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67169758 | TCTCTCTCTCTCTCT[-/C]CTTTTTTTTTTTTTT | 22992 |
rs772888557 | snp | A/G | 3.3618e-05 | 0.00409974 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67254215 | CAGGTCAGGACAATC[A/G]CAGCAAGCTCCGGAA | 22992 |
rs772891417 | snp | A/G | 1.66818e-05 | 0.00288802 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67250328 | GTTGCTGCGGCTGCA[A/G]GCCACAGAGCGCACC | 22992 |
rs772892608 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67248748 | AGCCAGTGAGTGCAG[C/T]AGTGTACTTGAGCTT | 22992 |
rs772902492 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67160280 | TTGATGTCTCTGGGT[A/G]TGCTGTTGCCATTTG | 22992 |
rs772915762 | in-del | -/AC | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67177776 | AATACATAAACCGGT[-/AC]ACAGTCATTTATTAT | 22992 |
rs772977471 | snp | A/G | 3.36101e-05 | 0.00409926 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67250228 | ACCCGGTTTCCCCCC[A/G]GGGTATGGTGACTCG | 22992 |
rs772990757 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67193980 | CCCAAATTGCTGAGA[G/T]TATAGGCGTAATCTC | 22992 |
rs773011343 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67208138 | TTGACAAGAATAATT[C/T]GTATTTTTATAAAGA | 22992 |
rs773013802 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67167153 | AAATATATGCATATT[C/G]TAGTAAAACCTTTGG | 22992 |
rs773090869 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67131802 | TGTTTGATTATGTTT[C/G]AAACAAAGATGGCAC | 22992 |
rs773106133 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67180577 | GGGTGGGATTCCATG[C/T]GCACCGTGCATCTTT | 22992 |
rs773144179 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67130387 | TCACCTCCAGTGATC[C/T]GCCCACTTCGGCCTC | 22992 |
rs773146180 | snp | A/T | 2.81901e-05 | 0.00375423 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67231587 | AGTTAAATGGGTTGG[A/T]GTCTGGGAATGGGGA | 22992 |
rs773187013 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67195170 | AGTTCTCTAGTCTAA[A/G]TAGTCTCAGTTTATC | 22992 |
rs773204001 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67188099 | TGTGCTCCTAGCCAC[A/T]TGGAAGGCTTGAGCC | 22992 |
rs773229399 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67138964 | AAGTTATTTTAAAAT[C/T]GTTTCTTCATATTTC | 22992 |
rs773239884 | snp | G/T | 2.44597e-05 | 0.00349704 | intron-variant | KDM2A | GRCh38.p7 | 11:67181417 | AGTGTTTTCAGCCTG[G/T]CTGGATGTAGTTGCA | 22992 |
rs773239947 | snp | G/T | 1.76505e-05 | 0.00297068 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67231670 | CTCACTAGCCCTGTA[G/T]CGAATGGAGTCAACC | 22992 |
rs773245830 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67165506 | AATCTTAAGTTTGAC[A/G]GTTTGAAATAGAGGT | 22992 |
rs773288212 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67227844 | CCAAGTACCCTTTAT[C/G]TTCAGTGATTGTTTC | 22992 |
rs773288530 | snp | C/T | 4.08438e-05 | 0.00451888 | intron-variant | KDM2A | GRCh38.p7 | 11:67217924 | TATTTAGCCATTTTT[C/T]TCCTTAATGAAAAAG | 22992 |
rs773288537 | snp | C/G | 1.65836e-05 | 0.0028795 | intron-variant | KDM2A | GRCh38.p7 | 11:67246134 | GAGGAGAGCTATGAG[C/G]GGTTCCTGAAGTCTC | 22992 |
rs773324257 | snp | C/T | 1.65784e-05 | 0.00287905 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67181867 | GGATCCAGACTTCAC[C/T]GTGAATGATGTCAAA | 22992 |
rs773347644 | snp | A/G | 3.32635e-05 | 0.00407807 | intron-variant | KDM2A | GRCh38.p7 | 11:67121403 | CCAGTTTTAAAGTAG[A/G]ATAACTATTTTGTTT | 22992 |
rs773351190 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67148943 | CTCAGCATTACAGAT[C/G]TACTTAAATCTTGTA | 22992 |
rs773369698 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67132486 | GACGGGGTCTCAACT[A/G]TTATTGGCCAGGCTG | 22992 |
rs773376828 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67204690 | TAGAGATGGGGTTTC[A/G]CCGTGATAGCCAGGA | 22992 |
rs773399442 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67140195 | ACATGGCGAAATCCC[A/G]TCTCTCCAAAAAATA | 22992 |
rs773412916 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67146716 | GGTTTTGATGTGTTG[C/G]CCAGATTGGTCTTGA | 22992 |
rs773414421 | in-del | -/GAGGAG | 1.72728e-05 | 0.00293872 | cds-indel, intron-variant | KDM2A | GRCh38.p7 | 11:67250596 | GAGGGGCTGGGGGGA[-/GAGGAG]GAGGAAGAGGAGGAG | 22992 |
rs773481875 | snp | C/G | | | upstream-variant-2KB, utr-variant-3-prime | KDM2A, LOC107984341 | GRCh38.p7 | 11:67117344 | AATATAGCGCTAACA[C/G]GCACTTTAGCTTGTC | 22992 |
rs773485389 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67167497 | TGTATATAAGTAGCT[A/G]TTTGACACTAGTTCT | 22992 |
rs773498361 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67176089 | CTTCTTTTGGCTTTT[A/G]AACTGTGATTTGTGG | 22992 |
rs773505281 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67189578 | GGCGAGGTGGCTCAC[G/T]CCTGTAATCCTAGCA | 22992 |
rs773520453 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67252039 | TGTGGTTTGTGGCCT[A/G]TAGATTTGTAGACTG | 22992 |
rs773535691 | snp | C/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67184400 | TTTGGGAGGCCGAGG[C/T]GGGCATATCACGAGG | 22992 |
rs773554417 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67226821 | GCTCTTTTATTTTCT[A/G]AAAGGGAAATGGGTT | 22992 |
rs773561725 | snp | C/T | 1.69352e-05 | 0.00290987 | intron-variant | KDM2A | GRCh38.p7 | 11:67254863 | TGTCATTATGTCCAC[C/T]TTCCCGACAGGTTGC | 22992 |
rs773611489 | snp | A/C | 1.68026e-05 | 0.00289845 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67180178 | AAACTGCACACCAAC[A/C]AATATAATGCCAATT | 22992 |
rs773639147 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67242927 | CTCAAGGGTACTGAG[A/G]CAGAGTCTGGATGCT | 22992 |
rs773642781 | in-del | -/AT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67236497 | ATAAAGTAGTTCTTA[-/AT]ATATATGCATATATA | 22992 |
rs773651283 | snp | A/G | 3.53826e-05 | 0.00420595 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67254980 | TCGAAAAGCCTGCGA[A/G]CACTTCATCTCAGAC | 22992 |
rs773662076 | snp | C/T | 0.000231849 | 0.0107643 | missense, nc-transcript-variant, intron-variant | KDM2A | GRCh38.p7 | 11:67243051 | GATCCCAAGTTAGCC[C/T]TCACTGGAGTTCCTA | 22992 |
rs773674137 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67163319 | GCAGGATACAGTTGT[G/T]GAATTTCATAAAATT | 22992 |
rs773678613 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67134832 | TAAATCTAACACAAA[A/G]CATCTCAAAAGCAGT | 22992 |
rs773718614 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67196824 | TGAATATATTTAATA[A/G]CACTGAACTGTGCTC | 22992 |
rs773728925 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67161685 | AGTGGTTCTCAACAT[A/G]TGGTCTGGGGATATA | 22992 |
rs773745622 | snp | A/G | 1.71314e-05 | 0.00292667 | missense, intron-variant | KDM2A | GRCh38.p7 | 11:67250632 | GAGGAGGAGGAAGAT[A/G]ACAGTGCAGAGGAGG | 22992 |
rs773750696 | snp | A/G | 0.000185891 | 0.00963903 | missense, intron-variant | KDM2A | GRCh38.p7 | 11:67240271 | AGAGGCAGAATATCT[A/G]ACTCCTTCAGGAGAA | 22992 |
rs773750703 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67148347 | GGTCGCTTGACCCCC[A/G]GAGGTTGAGGCTGCA | 22992 |
rs773761684 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67216199 | TCCTGTTTCTAGATT[C/G]CTGAATCAGAGTTCT | 22992 |
rs773764851 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67184281 | GGAGGGTCACTTGAG[C/G]TCAGGAGTTTGAGAT | 22992 |
rs773768436 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67154062 | TTCCATAATGTCTAA[C/T]ATTTAGAATTTTCCA | 22992 |
rs773793978 | snp | G/T | | | intron-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67120235 | GCCCAGGCGGTCGTC[G/T]CCCAGGGGGTGCAAG | 22992 |
rs773803220 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67149838 | TGATTCTCCTGCCTC[A/G]GCCACCCAAGTAGCT | 22992 |
rs773820946 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67237549 | GCAATCCTCCTGCCT[C/T]GACCTCCCAAGTGCT | 22992 |
rs773824045 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67251803 | CTCTAAATAGACCCT[A/G]TTCTTTGCAAACATG | 22992 |
rs773836437 | snp | C/T | 1.67483e-05 | 0.00289377 | missense, nc-transcript-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67207600 | GCTACTATGAGACCC[C/T]AGAGGAGGAGCGAGA | 22992 |
rs773837294 | snp | A/G | 1.82191e-05 | 0.00301815 | missense, intron-variant | KDM2A | GRCh38.p7 | 11:67250762 | GCCGCAGAGAACTTT[A/G]TGAATGTATGCGAGT | 22992 |
rs773857530 | snp | A/G | 0.000560695 | 0.0167342 | synonymous-codon, intron-variant | KDM2A | GRCh38.p7 | 11:67240237 | ATTCCAGAATATTCA[A/G]GTAAATCCGGATTTT | 22992 |
rs773882833 | snp | A/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206143 | TGAGATTTAAACTTA[A/G]GTCTCAGGCAGGTGC | 22992 |
rs773889811 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67156680 | GCCGAGATGGCGCCT[C/T]TGCACTCCAGCCTGG | 22992 |
rs773900159 | snp | C/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185050 | ATTGTGGATCTAATA[C/G]ACAAAGATTTTTAAA | 22992 |
rs773908062 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67236757 | CTTAATAAGCAGTGC[A/G]TTATTACAGCCAGAA | 22992 |
rs773944858 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67186815 | GTATATGCCTGTAAT[C/T]CCAGCTACTCAGTAG | 22992 |
rs773945894 | snp | A/G | | | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67238713 | CTGTCCTGGAAATAA[A/G]TAAGAATGCTTAAGA | 22992 |
rs773947282 | snp | A/T | 1.6617e-05 | 0.00288239 | missense, nc-transcript-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67207581 | ACCATGGCTCAGTGG[A/T]CACGCTACTATGAGA | 22992 |
rs773979665 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67134075 | TTTTGAAGGCAAAGA[C/T]AAATGAAATACTAAG | 22992 |
rs774024462 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67121421 | AACTATTTTGTTTCC[A/C]GTTGTGAATATACTG | 22992 |
rs774036260 | snp | A/G/T | 7.80174e-05 | 0.00624528 | intron-variant | KDM2A | GRCh38.p7 | 11:67215458 | AGAAGTAAGTGATGC[A/G/T]CCCTGCATCTTCCTC | 22992 |
rs774036993 | snp | C/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206845 | GTTTTGTTGTAGTTG[C/T]TATAGTTAACAAGAA | 22992 |
rs774052517 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67208044 | TCAAAAATTTAAAAT[A/G]AAATGCGTTGTTTTT | 22992 |
rs774061200 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67126665 | GTGAGCTGAGATCAC[A/G]CCACTGCACTCCAGC | 22992 |
rs774105602 | snp | C/T | 3.31214e-05 | 0.00406935 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67228126 | AACCAACCGTTCCCA[C/T]CTAACTAAGGAATTT | 22992 |
rs774117100 | snp | A/G | 1.65993e-05 | 0.00288086 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67253454 | TCCATCCATTGCAGG[A/G]CTGAAAGACCTCCTC | 22992 |
rs774161687 | snp | A/C/T | 1.6596e-05 | 0.00288058 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67245228 | GTGCGGGTTCCTACC[A/C/T]TCCCCATTACGAAGC | 22992 |
rs774175960 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67232573 | CATGTGCCATGTCAG[-/T]TTGCTGCACCCATTG | 22992 |
rs774191825 | snp | G/T | 3.61474e-05 | 0.00425116 | intron-variant | KDM2A | GRCh38.p7 | 11:67180253 | AGCTTACAGTCCTTT[G/T]ATGTGGGAAGCCATA | 22992 |
rs774206635 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67180284 | GACTCTGAGCATTGG[A/G]GGTTTAGCCTTTATC | 22992 |
rs774206731 | snp | C/T | 1.65886e-05 | 0.00287993 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67253601 | GCTTACTCCACCGGC[C/T]GATAAACCAGGTATG | 22992 |
rs774218403 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67232487 | TCAAGTTTTATGTTT[A/G]TTTATTTTTTAATTA | 22992 |
rs774231018 | in-del | -/TTG | | | intron-variant | KDM2A | GRCh38.p7 | 11:67138869 | TGAGAACCATTGGAA[-/TTG]TTGTAGCAGTTTTTC | 22992 |
rs774258549 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67174675 | TTATATAGTTAATTA[C/T]GACTAAACTGGGAAT | 22992 |
rs774287881 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67190403 | TGACAAGAGCAAACC[C/T]CCGACTCAAAAAAAG | 22992 |
rs774293254 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67141788 | CTGTATGTTCATGCC[C/T]ATTAACCATCCTCTC | 22992 |
rs774294150 | snp | A/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67179145 | TTGCATTTTTCTAAT[A/G]ACTAATGAGAATTGA | 22992 |
rs774319441 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67234295 | AACTTGGTGCTTATA[C/G]CACTGATGGCTATAC | 22992 |
rs774376270 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67167060 | TCCAGCCTAGGCGAC[A/T]GAGCGAGACTCTGCC | 22992 |
rs774378573 | in-del | -/TTTA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67122643 | TATTTTTTATTTATT[-/TTTA]TTTATTTATTTATTT | 22992 |
rs774400800 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67228299 | ACCAAATTCATCACT[G/T]GAATTGAATACCAGT | 22992 |
rs774404194 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67241317 | AACAGAAAAGGATGC[C/T]ATAGCAACTTGAAGT | 22992 |
rs774414640 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67153938 | TGAGTTATTTGAAAG[C/T]AATTTGCATACATCA | 22992 |
rs774415318 | snp | A/G | 0.000170774 | 0.00923892 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67231573 | ATTGGTAGATTTGGA[A/G]TTAAATGGGTTGGAG | 22992 |
rs774421563 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255244 | CTTATCTGCCTGCTC[C/T]TCTCCCTCCTAAGGA | 22992 |
rs774459181 | in-del | -/C | 1.68216e-05 | 0.00290009 | frameshift-variant, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67250221 | TCCATGACCCGGTTT[-/C]CCCCCCGGGGTATGG | 22992 |
rs774495089 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255795 | GAACTGTCTACCCCA[A/G]GGACACACCCATTTC | 22992 |
rs774498148 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67194213 | CTCAGTTCTTGCTTC[A/G]ATGACAGCAAATAAA | 22992 |
rs774505188 | snp | C/T | 3.32795e-05 | 0.00407905 | intron-variant | KDM2A | GRCh38.p7 | 11:67217920 | GGGTTATTTAGCCAT[C/T]TTTTTCCTTAATGAA | 22992 |
rs774521256 | snp | C/T | 3.31246e-05 | 0.00406955 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67245301 | CAGCTGCTGCCTCCC[C/T]GATTGTGTCAGGAGC | 22992 |
rs774535266 | snp | C/T | 1.7011e-05 | 0.00291637 | intron-variant | KDM2A | GRCh38.p7 | 11:67245499 | TTTGGGGAGGGGTGG[C/T]AGTGCCAAAGGAACT | 22992 |
rs774536418 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67201346 | CTGTAGATGCCATTA[A/T]GAACATATTTATGGC | 22992 |
rs774576742 | snp | A/G | 8.55103e-05 | 0.00653818 | missense, intron-variant | KDM2A | GRCh38.p7 | 11:67250570 | CCCGAACCCCCCAGC[A/G]TGGGGATGAGGAGGG | 22992 |
rs774615025 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67137325 | TTTGGACCAATGTCA[A/G]TGGTTGCAATGTAGA | 22992 |
rs774627964 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67174731 | AATTCTTCATATTAT[G/T]TGGATTCTAAATAAC | 22992 |
rs774646240 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67138767 | GGATCCTACCCCAAA[C/T]GTACTGAATCAGAAA | 22992 |
rs774652519 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67215273 | ATTCTGCTTTTCTTG[A/C]CTTTAAAATTATCTT | 22992 |
rs774690714 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67240501 | TGTTACTTCGTGTTG[A/C]TTGAGCCGTCATTGC | 22992 |
rs774762348 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67210928 | GGGCGTATCACTTGA[A/G]CCCAAGAGTTCGAGA | 22992 |
rs774779243 | snp | A/G | 1.72719e-05 | 0.00293865 | missense, intron-variant | KDM2A | GRCh38.p7 | 11:67250599 | GGGCTGGGGGGAGAG[A/G]AGGAGGAAGAGGAGG | 22992 |
rs774795323 | snp | A/G | 2.01201e-05 | 0.0031717 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67219384 | AGTTAAAAATATACA[A/G]CATTGAAGATCGGAC | 22992 |
rs774800185 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67124488 | GGCTAATTTTTTTGT[A/G]TTTTTAGTTGAGACG | 22992 |
rs774807482 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67165052 | AAGAGGTCTTGCCAG[G/T]ACTGTAATGTAATGG | 22992 |
rs774811418 | snp | A/G | 1.72261e-05 | 0.00293475 | intron-variant | KDM2A | GRCh38.p7 | 11:67254844 | GCTGTGTGTATGTGA[A/G]CACTGTCATTATGTC | 22992 |
rs774829997 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67246349 | CCCAGTTCCTGTCCT[C/G]ATGGAGCTTAGAATC | 22992 |
rs774834862 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67218607 | TTTTATTTTATTTAT[G/T]TATTTATTTATTTTG | 22992 |
rs774841382 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67227550 | TCTTGGTGGTTCTAA[A/G]TGGTCTTCCTCAAGT | 22992 |
rs774882809 | snp | C/T | 3.31901e-05 | 0.00407356 | intron-variant | KDM2A | GRCh38.p7 | 11:67121389 | CCCCACCACACCCTC[C/T]AGTTTTAAAGTAGGA | 22992 |
rs774898626 | snp | A/G/T | 3.31231e-05 | 0.00406948 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67231824 | GTGCTCCCCGAAAGG[A/G/T]CAGGCAAGTGCATCT | 22992 |
rs774904045 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67196677 | TATATAGAGTAACCA[A/G]AATCATGGAGACAAA | 22992 |
rs774904372 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67189367 | CACAGCCTACCAAAA[C/T]TTATAGGGATCAGTG | 22992 |
rs774909319 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67161628 | CACACTGTTGTGACC[C/T]AAATTGATTTTTGTG | 22992 |
rs774909401 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67195646 | TTCCTTTTATTTTTA[C/T]TAGTTGTTCATGCTC | 22992 |
rs774933523 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67148274 | TAAAAAAAAAAATTT[A/G]GCTGGGCGTGGCGGT | 22992 |
rs774935445 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67133148 | CTTGTTGGCCAGGCT[C/G]GAGTGTAATGGTGCT | 22992 |
rs774945873 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67149836 | AGTGATTCTCCTGCC[C/T]CAGCCACCCAAGTAG | 22992 |
rs774967696 | snp | G/T | 1.65351e-05 | 0.00287528 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67254967 | GCAAGCAGATCACTC[G/T]AAAAGCCTGCGAGCA | 22992 |
rs774979331 | snp | C/T | | | upstream-variant-2KB, utr-variant-3-prime | KDM2A, LOC107984341 | GRCh38.p7 | 11:67117557 | TCCTGAAAGAGTTGA[C/T]GGCTGTTTATGCAGG | 22992 |
rs774982555 | snp | A/G | 1.66134e-05 | 0.00288208 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67231752 | AAACTTTGGCTGGGG[A/G]CTCATCTTCTGACTG | 22992 |
rs774984510 | snp | C/T | 0.000232057 | 0.0107692 | synonymous-codon, intron-variant | KDM2A | GRCh38.p7 | 11:67250463 | CACCAAAGAGCTCCA[C/T]GGGACATCCATTGTG | 22992 |
rs775002997 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67181070 | ATATTATTTAAGCTC[G/T]AAATTTCCTGTGGAA | 22992 |
rs775004412 | in-del | -/AAAAAAAAAAAAGG | | | intron-variant | KDM2A | GRCh38.p7 | 11:67221021 | CTGTCTGACCCGAAA[-/AAAAAAAAAAAAGG]AAAAAAAAAAAAGGT | 22992 |
rs775028518 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67184020 | GGGCAATTCCTTGAG[C/T]CCTGGAGGCTGAGAC | 22992 |
rs775048375 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67233591 | TGGGAGGCAAAGGTT[A/G]CAGTGAGCCGAGATT | 22992 |
rs775074486 | snp | A/T | 1.65622e-05 | 0.00287764 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67231813 | GGATCCCCAGTGTGC[A/T]CCCCGAAAGGACAGG | 22992 |
rs775082080 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67251686 | CGCTCCTCCAGGGGA[C/T]TCTGATGCATGCTCG | 22992 |
rs775082275 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67236178 | CTCTGTCACCCAGGC[C/T]GAAGTGCAGTGGCGT | 22992 |
rs775087262 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67217441 | GCCAGACAGAGTGTT[G/T]AAGGGACTGCCTAGG | 22992 |
rs775095322 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67134021 | AAACAAGAAAACTGA[A/C]CTGTCCTTGTTGAAG | 22992 |
rs775124030 | in-del | -/GATG | | | intron-variant | KDM2A | GRCh38.p7 | 11:67196778 | GAACAGAGTTATGGA[-/GATG]GATGGTGGTAATGGT | 22992 |
rs775131036 | snp | G/T | 0.000101817 | 0.00713431 | missense, nc-transcript-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67207525 | GGAGTCGTCGCATGG[G/T]GGATGTCATGGACGT | 22992 |
rs775142669 | snp | A/C | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67184951 | CAATTTTCAACAAAA[A/C]ATCATAAGGCATACG | 22992 |
rs775188579 | in-del | -/AA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67194033 | GATACTAATCTTGCC[-/AA]AGTTATTTTTAAAAT | 22992 |
rs775237812 | in-del | -/AAC | | | intron-variant | KDM2A | GRCh38.p7 | 11:67233653 | GTGAAACCCTGTCTC[-/AAC]AACAACAACAACAAA | 22992 |
rs775306998 | snp | C/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206827 | ACTCTTGTGGCCTTA[C/T]GCGTTTTGTTGTAGT | 22992 |
rs775310467 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67126333 | TATTCCCAGCACTTC[A/G]GGAGGCCAGGGAGGG | 22992 |
rs775316724 | snp | C/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67205808 | ATTGTCAGCTTTTTA[C/T]TTTCTCTCCCTTCCT | 22992 |
rs775346138 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67245044 | ATGAGTTGTGTGTCA[A/G]TAAAATTTATTCTAG | 22992 |
rs775348492 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67237384 | AACTAGAAGAAGACC[A/C]AGTATAGTTAGCTCT | 22992 |
rs775356668 | in-del | -/CTT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67169759 | TCTCTCTCTCTCTCT[-/CTT]TTTTTTTTTTTTTTG | 22992 |
rs775385538 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67157000 | TTTAAAATATTTACC[C/T]TCTGGCCCCTTTCAT | 22992 |
rs775390199 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67257550 | GCCTCCATCTTTCCA[A/G]GCACCGGGGCGAAAA | 22992 |
rs775402349 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67192532 | TCACTGCAACCTCCA[C/T]CTCCCAGGTTCAAGC | 22992 |
rs775404362 | snp | C/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67177399 | AGATACATTATACCA[C/T]GTACAAAAGCATTTT | 22992 |
rs775415114 | snp | C/T | | | intron-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67120205 | CTTTTTCCTCTCCGG[C/T]CCTGGCTGCTCCATG | 22992 |
rs775424494 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67191246 | TGGCCAGGATGGTCT[C/G]GATCTCCTGACCTCG | 22992 |
rs775431857 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67222057 | TGTTTAACTCTGTCA[C/T]TCTTTTTTTTTTTTT | 22992 |
rs775436611 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67155389 | TCATGGTTCATTGCA[A/G]CGTCATACTCCTAGG | 22992 |
rs775465805 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67246453 | CCTTTAGGCATCTCT[G/T]ATACATACTTCAGTG | 22992 |
rs775471379 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67199626 | GGCTGAGAGAGGTGA[C/G]GGAGCTGCAGAAGAA | 22992 |
rs775483478 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67171292 | TAGTCAGGACAGACG[A/T]GGCCGAGTCTGAAAT | 22992 |
rs775491984 | snp | C/T | 0.0001628 | 0.00902073 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255574 | GTCCCAGACCCGTGC[C/T]GATCACACTGGTGCT | 22992 |
rs775503199 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67127914 | TTTCACCATGTTAGC[A/C]AGGCTGGTTTCAAAC | 22992 |
rs775505210 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67187669 | AACCTCTGTCTCCTG[A/G]TTCAAGCGATTCTCC | 22992 |
rs775548814 | snp | A/C/T | 8.29241e-05 | 0.00643863 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67253597 | ACTTGCTTACTCCAC[A/C/T]GGCTGATAAACCAGG | 22992 |
rs775554301 | snp | A/G | 2.91984e-05 | 0.00382078 | intron-variant | KDM2A | GRCh38.p7 | 11:67252641 | AAGCAGCCTGTGATG[A/G]GAGCTCCACTGATCA | 22992 |
rs775560819 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67165973 | CATGACCAGTACCAT[A/G]TATTATACTGATGAC | 22992 |
rs775640061 | snp | C/T | 3.31587e-05 | 0.00407164 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67245248 | CATTACGAAGCCTCA[C/T]ACTATGAAACCAGCT | 22992 |
rs775656106 | snp | A/C | 2.06166e-05 | 0.00321059 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67181377 | CTCTGATTTTCAAGA[A/C]TTCTGATGGACTCGG | 22992 |
rs775659911 | snp | C/G | | | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67239079 | TGTCTTGACAGGATG[C/G]AGGACTGGCTGCTTC | 22992 |
rs775659922 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255135 | CTCCTCGACCCTGCA[C/T]GGGCTCTGAGGCCAG | 22992 |
rs775663248 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67214827 | CTTGAAAAGACATGA[C/T]AGACCTGGAGCTTCT | 22992 |
rs775672571 | snp | C/T | 0.000280544 | 0.0118403 | intron-variant | KDM2A | GRCh38.p7 | 11:67252510 | AAAGCGTCTAGTTGT[C/T]GTAGAGTTCAAGGCA | 22992 |
rs775720275 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67151812 | GTAGTATGGCTTTAT[C/G]TAGCTTACTATAGCC | 22992 |
rs775727547 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67225529 | TAATCCCAGCACTTT[A/G]GGAGGCCGAGGTGGG | 22992 |
rs775807056 | in-del | -/TCTT | 6.53958e-05 | 0.00571783 | intron-variant | KDM2A | GRCh38.p7 | 11:67181292 | TAATTATACCACTTA[-/TCTT]TCTAATATTTTCCTA | 22992 |
rs775843110 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67200642 | CTCAGCCTTTAGCTG[G/T]GACTACAAGCACATG | 22992 |
rs775861602 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67215657 | GAAAAAAAACTTACA[A/T]TTTAGTCAATACGGT | 22992 |
rs775880574 | in-del | -/TTTC | | | intron-variant | KDM2A | GRCh38.p7 | 11:67169359 | TAGTGACAAGATTGG[-/TTTC]TTTCTTTCTTTCTTT | 22992 |
rs775915562 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67240718 | CACCCCCGCTCTCCT[A/G]TCCCAAACCCCCTCT | 22992 |
rs775936151 | snp | A/G | 1.67922e-05 | 0.00289755 | intron-variant | KDM2A | GRCh38.p7 | 11:67245478 | GTGATCTGCTGGGTA[A/G]AGAATTTTGGGGAGG | 22992 |
rs775946914 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67248808 | CTTCACTTTTGTGGC[C/T]TGGCAGAAAGCCCTG | 22992 |
rs775998377 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67135365 | CACCGCGCCCAGCAC[A/T]GATTTCCTTTTGATA | 22992 |
rs776008942 | snp | G/T | 5.68553e-05 | 0.00533146 | intron-variant | KDM2A | GRCh38.p7 | 11:67217702 | TCATGTCAATGGCTG[G/T]TAACAGACTAAAGTT | 22992 |
rs776031985 | snp | A/G | 6.66001e-05 | 0.00577023 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67250339 | TGCAGGCCACAGAGC[A/G]CACCATGGTACGGGA | 22992 |
rs776037478 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67202443 | TTTGTGAAAGGAAGT[A/G]TCAATCCATGTTGCA | 22992 |
rs776038143 | snp | A/G | 1.6654e-05 | 0.00288561 | intron-variant | KDM2A | GRCh38.p7 | 11:67254442 | CTACAGTTGTTCATA[A/G]TCAGCGGTGCCCCCT | 22992 |
rs776039082 | snp | C/G | 1.67933e-05 | 0.00289765 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67250242 | CGGGGTATGGTGACT[C/G]GGTCATCCCCTGGGG | 22992 |
rs776098545 | snp | A/G | 2.37578e-05 | 0.00344649 | intron-variant | KDM2A | GRCh38.p7 | 11:67217888 | TCATTCCCTCAGGTA[A/G]GCAAAATGGGAAGAG | 22992 |
rs776105012 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67123207 | TCTTGAACTCCTGGC[A/C]TCAAGCGATCCTCCC | 22992 |
rs776111311 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67214792 | TAGTTTTATAGATGA[C/G]TTTGAGGGCCTTATA | 22992 |
rs776122447 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67131945 | TGTTTTCTGTTTTAA[A/G]TTTTAGGTTCTTGGG | 22992 |
rs776130082 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67160344 | GGTTTAGGAAGAGAT[A/T]ATAGCTTGAACCATT | 22992 |
rs776191813 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67246271 | ATCAGCCCTTGATTC[A/G]TATATGTACAATGTG | 22992 |
rs776282931 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67131479 | TGTAGTGGTGCGATA[C/T]TGGCTCACTGAAACC | 22992 |
rs776318089 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67194148 | TTTAATCCTTTTGTT[G/T]CTTTTCTAGTATTAG | 22992 |
rs776320516 | snp | A/G | 1.66651e-05 | 0.00288657 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67250334 | GCGGCTGCAGGCCAC[A/G]GAGCGCACCATGGTA | 22992 |
rs776321229 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67149805 | GGCTCACTGCAACCT[C/T]GGCCTCCCAGGTTCA | 22992 |
rs776326333 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67236038 | AGAAAAAGTGTATGC[A/G]TATTTGTGCATTGCA | 22992 |
rs776327687 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67229535 | GCTTTAGCATTTTAC[C/T]TTTACTGCATAATTT | 22992 |
rs776342613 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67124329 | TTTATATATATTTTT[G/T]GAAATGGAGACTCAC | 22992 |
rs776370457 | snp | A/C | 1.85751e-05 | 0.00304749 | intron-variant | KDM2A | GRCh38.p7 | 11:67217714 | CTGTTAACAGACTAA[A/C]GTTTTTTAACTCACA | 22992 |
rs776374880 | in-del | -/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67160199 | TCTGTTAGGAACAGG[-/C]AGTGATGTTGTATTT | 22992 |
rs776398252 | snp | A/C | 1.74729e-05 | 0.0029557 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67252845 | CTGACATGGCTCGTC[A/C]ATAGGCTGCCAGGTA | 22992 |
rs776413447 | snp | A/G | | | missense, intron-variant | KDM2A | GRCh38.p7 | 11:67250546 | GTGTGCTAGTGCAGC[A/G]CTGCCCAGCCCGAAC | 22992 |
rs776416367 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67155212 | GTAGAGATGGGGTTT[A/T]GCTATGTTGGCCAGG | 22992 |
rs776423151 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67182686 | TGCAGGCATGTGCCA[A/C]CAGGCCCGGCTAATT | 22992 |
rs776423751 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67256047 | CTGGTTTAGCGGAGC[C/T]CCCTGAGCCCAGGCC | 22992 |
rs776426625 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67189733 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 22992 |
rs776439500 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67195465 | TTTATTTTCTTTTTA[A/T]ACTCTTCTATTTTCC | 22992 |
rs776490911 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67257396 | GTTTTTAGAGGTGAG[A/G]GTTGGTCCATGTGGA | 22992 |
rs776538118 | snp | G/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67205632 | TTTTTTGTTTTGTGT[G/T]TGTGTATGTTTAATT | 22992 |
rs776550109 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67232930 | GGCCAGGCTGGTCTC[A/G]AACTCTTGACCTCAG | 22992 |
rs776553480 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67132975 | ACACATTGGCAGTGA[A/T]GGACTGACTAAACTT | 22992 |
rs776562441 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67204835 | GTTGTAGCATGTATT[A/G]GTACTTCATTCCTTT | 22992 |
rs776577139 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67126246 | GCAAAACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 22992 |
rs776578039 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67199017 | CTCCTGACCTCAAGT[A/G]ATTCACCCGCCTTGG | 22992 |
rs776578589 | snp | A/G | 1.66048e-05 | 0.00288134 | intron-variant | KDM2A | GRCh38.p7 | 11:67181902 | GTGTGGGTAAGTGTC[A/G]AGCTTTTGGCCTCTG | 22992 |
rs776609835 | snp | A/G | 1.66726e-05 | 0.00288722 | intron-variant | KDM2A | GRCh38.p7 | 11:67245936 | AGGGAAACTGAAATG[A/G]TAAAGATCTGAGTCA | 22992 |
rs776619525 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67183798 | AGTGCTGCTTCTGAT[C/G]ACAGAAGTACAGACA | 22992 |
rs776642326 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67127183 | CCTCTTTGTAGCCTC[A/G]ACCGCCTGGCTCAAG | 22992 |
rs776654358 | in-del | -/GAG | | | cds-indel, intron-variant | KDM2A | GRCh38.p7 | 11:67250608 | GGAGAGGAGGAGGAA[-/GAG]GAGGAGGAGGAGGAG | 22992 |
rs776670262 | snp | C/T | 1.76727e-05 | 0.00297255 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67207475 | TAAGGATATTAGTGG[C/T]TCGATAGAGATGATC | 22992 |
rs776671138 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67134564 | GGCTGGAATGTAGTG[A/G]TGCGATCTCGGCTCA | 22992 |
rs776684691 | snp | G/T | 1.67089e-05 | 0.00289035 | intron-variant | KDM2A | GRCh38.p7 | 11:67253431 | CAGTGTATTATTACA[G/T]GTCTCATTCCATCCA | 22992 |
rs776702207 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67214677 | GGTTCTCACTGTGTT[G/T]CCCAGGCTGGTCTTA | 22992 |
rs776723574 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67141216 | CATTTCTTCATATGC[A/G]AAACAATTTTTCCAT | 22992 |
rs776747524 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67169113 | GGCGCCTGCCACCGC[A/G]CCTGGCCAATTTTTG | 22992 |
rs776785040 | snp | A/G | 3.31214e-05 | 0.00406935 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67228116 | TGTACTGCATAACCA[A/G]CCGTTCCCACCTAAC | 22992 |
rs776789718 | snp | G/T | 1.76839e-05 | 0.00297349 | intron-variant | KDM2A | GRCh38.p7 | 11:67180233 | GTCAGTATTGTTTTG[G/T]TTCCAGCTTACAGTC | 22992 |
rs776791018 | snp | A/G | 1.91181e-05 | 0.00309171 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255009 | ACTTGTCCATCAACA[A/G]CCTCTACTGCCTGTC | 22992 |
rs776804626 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67244350 | TGTCTGCTATCTACC[A/G]GTTCGTATGCTTGAA | 22992 |
rs776815394 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67190983 | GAATTCTACCAAACA[C/T]TTAAAGAGGAACTAA | 22992 |
rs776875031 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67246570 | GCAGAGCTAAATAGC[-/T]TTTAAAAAAAAAAAG | 22992 |
rs776883963 | snp | A/G | 4.38375e-05 | 0.00468154 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67181328 | GTGACAGATTTTAAT[A/G]TAGAGTATATTCAGC | 22992 |
rs776898974 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67199507 | CCTTATCACTGATAA[C/T]GGAGAAAGTCTGAGT | 22992 |
rs776916084 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67212917 | AACACACGGGGATGG[A/G]AGATGGTGGCTACTA | 22992 |
rs776926848 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67253973 | GCACATAGCCTTTTG[C/T]TGTGTGCATGAGGCA | 22992 |
rs776928080 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67253334 | TGGATGACTAAAAGA[-/T]TAGGCATAGTCCTTC | 22992 |
rs776966772 | snp | C/G | 1.7144e-05 | 0.00292775 | missense, intron-variant | KDM2A | GRCh38.p7 | 11:67250648 | ACAGTGCAGAGGAGG[C/G]GGGTGCAGCCAGGCT | 22992 |
rs776971157 | in-del | -/TGTG | | | intron-variant | KDM2A | GRCh38.p7 | 11:67172619 | TAGCTCTTATAGTTG[-/TGTG]TGTGTGTGTGTGTGT | 22992 |
rs776999459 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67230006 | ATGGTGAAACCCCGT[C/G]TCTACTAAAAATACA | 22992 |
rs777014835 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67251950 | ATCAGATTCCCGTTA[C/T]GTGCTGTCTCTCTTC | 22992 |
rs777053532 | snp | C/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67186345 | GGAGGCAGTGAGCCA[C/G]TGTATTCAAAGTGCT | 22992 |
rs777091585 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67150057 | CTCAGTAAACAAAAG[A/G]TAGCAAAATTCAACA | 22992 |
rs777107740 | in-del | -/CATTT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67187185 | AGAAAGGAATTTACA[-/CATTT]CACCAAATAAATGTA | 22992 |
rs777136756 | snp | A/G | 1.65641e-05 | 0.00287781 | missense, nc-transcript-variant, intron-variant | KDM2A | GRCh38.p7 | 11:67243073 | GAGTTCCTATAGTAC[A/G]GTGGCCAAAAAGGGA | 22992 |
rs777141391 | snp | A/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185292 | TTAAGTCTAAGGAAC[A/G]GAATGACAAAAATTG | 22992 |
rs777146533 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67164827 | TGGTCTTGAACTCCT[A/G]ATCTCAAGTGATCTA | 22992 |
rs777169951 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67221126 | AGCCTCCACCTTAGA[A/G]AATGAGAGCTTATTT | 22992 |
rs777226416 | snp | C/T | 1.65861e-05 | 0.00287972 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67245238 | CTACCATCCCCATTA[C/T]GAAGCCTCACACTAT | 22992 |
rs777229701 | in-del | -/G | 1.65921e-05 | 0.00288024 | frameshift-variant, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67245407 | GACATGAAGAAGTTT[-/G]GGGGGGCCTGGACGC | 22992 |
rs777246618 | snp | C/T | 1.65776e-05 | 0.00287898 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67245389 | TGTTTGCCACTACTG[C/T]AGAGACATGAAGAAG | 22992 |
rs777254200 | in-del | -/TTC | | | intron-variant | KDM2A | GRCh38.p7 | 11:67229483 | TCCTGGGATCACATG[-/TTC]TTATGGAATCTTTAA | 22992 |
rs777263835 | snp | C/G | | | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67238899 | GTACACTGTGGATCA[C/G]TAGAAACTCAACCAG | 22992 |
rs777302877 | in-del | -/T | | | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67239894 | AGACAGGGCGGGGGC[-/T]TGTGGCTGAGCTCTC | 22992 |
rs777314291 | snp | C/G/T | 3.82491e-05 | 0.00437303 | intron-variant | KDM2A | GRCh38.p7 | 11:67217682 | AGTTGAGGGAGACGA[C/G/T]TGGGTCATGTCAATG | 22992 |
rs777336448 | snp | C/T | 1.75903e-05 | 0.00296561 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | KDM2A | GRCh38.p7 | 11:67217788 | TACGAGAATTGGCTG[C/T]TGTCAGGGAAACAGG | 22992 |
rs777346297 | snp | A/T | 1.65647e-05 | 0.00287786 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67254400 | ACTCGCTACTCTCTC[A/T]CAGAGCTCAATATGG | 22992 |
rs777351174 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67175483 | CTGTTGCCAACTTTC[C/T]AGTTGCAATAATCAA | 22992 |
rs777357670 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67138153 | GTTGAGTGAAATGCC[A/G]TTAAGTGGCACAAGT | 22992 |
rs777359376 | snp | C/T | 1.65982e-05 | 0.00288077 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67245227 | GGTGCGGGTTCCTAC[C/T]ATCCCCATTACGAAG | 22992 |
rs777379030 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67146241 | CTCCTGATCTGCCTG[C/T]CTCAGCCTCCCAAAG | 22992 |
rs777437435 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67173843 | CCAGTCTCCTGAGTA[C/G]TACAGGCGCACATTA | 22992 |
rs777437625 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67189086 | CAGACACAGACAGAA[C/T]CCTACCTAACAGCAA | 22992 |
rs777439404 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67182533 | AATTGAATAAGTCTT[-/T]TTTTTTTTTTTTTTT | 22992 |
rs777442959 | snp | C/T | 1.66183e-05 | 0.00288251 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67252745 | GAGTAGGTGTAAGGC[C/T]ATTGTGCCCCAGGCC | 22992 |
rs777444558 | snp | A/C | 3.31367e-05 | 0.00407029 | intron-variant | KDM2A | GRCh38.p7 | 11:67215984 | AGGGGTTGGAATCTG[A/C]AGTTGGTTGTATGAC | 22992 |
rs777453102 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67192896 | CAAAGTGATTGTACC[A/G]GTTTACACTTTGTTG | 22992 |
rs777474782 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67125623 | CTAAAAATACAAAAA[C/T]TAGCTGGGCACTGGG | 22992 |
rs777492206 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67153150 | CCACCACGCCCAGCT[A/G]ATTTTTGTATTTTTA | 22992 |
rs777527172 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67216954 | AACAACAAAAAAACA[A/T]GAGGTCTTGTCCGGG | 22992 |
rs777561610 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67209918 | TTGGAAACTTAGCCA[C/G]GCATGGTGGCATGCA | 22992 |
rs777573593 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67162554 | GCATTTATAGGCATG[C/T]GCCACCACACCCAGC | 22992 |
rs777607633 | snp | A/C/G | 0.00010022 | 0.00707819 | missense, intron-variant | KDM2A | GRCh38.p7 | 11:67250531 | TTCGCCATTCCCCCC[A/C/G]TGTGCTAGTGCAGCA | 22992 |
rs777629476 | snp | A/G | 1.65842e-05 | 0.00287955 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | KDM2A | GRCh38.p7 | 11:67121334 | GGAACCCGAAGAAGA[A/G]AGGATTCGTTACAGC | 22992 |
rs777644492 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67134551 | AATCTGTTGCCGAGG[C/T]TGGAATGTAGTGGTG | 22992 |
rs777674800 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67236698 | TTTCTCCTCTATAAA[A/G]TATCTGTGAGATTGT | 22992 |
rs777702325 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67183612 | CAGTTAATTTCAGTC[A/C]GTTTCAGGCCTTAGC | 22992 |
rs777734829 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67147392 | CTAAAAATAAAGAAA[A/G]TTAGCCGGGTGTGGT | 22992 |
rs777759694 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67212088 | ATTGCTTGAGCCCAG[G/T]AGTTTGAGGCAGCCT | 22992 |
rs777761260 | in-del | -/TTTTTTTTTTTTTTTTTTTTTGGGGGG | | | intron-variant | KDM2A | GRCh38.p7 | 11:67128014 | ACACCCGGCCTTTTT[-/TTTTTTTTTTTTTTTTTTTTTGGGGGG]TTTTTTTTTTTTTTT | 22992 |
rs777771534 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67251142 | TCAGCTGAACTCATC[A/C]CATGTTGGTTGAGAG | 22992 |
rs777787549 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67190658 | CCCAGCTACTCAGGA[G/T]GCTGAGTCATGAGAA | 22992 |
rs777821199 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67132854 | TCTGGAGTTGGGGCC[C/T]AGCAATCTGTGTTTT | 22992 |
rs777857459 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67155355 | TGTTGCCCAGGCTGG[A/T]GTGCAAGCAGTGGAC | 22992 |
rs777882479 | snp | A/G | 0.000187635 | 0.00968412 | intron-variant | KDM2A | GRCh38.p7 | 11:67196375 | GAAATCCTGGACTCA[A/G]GCGATCTTCCTGCTT | 22992 |
rs777884298 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67235673 | GTCACCTAGGCTGGG[A/G]TGCAGTGGCGCCATC | 22992 |
rs777919096 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67237629 | GTTTGTTTGTCCTGG[A/G]TCCAGGCTTACAGAT | 22992 |
rs777929754 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67119972 | AAACCGAAGACGACG[C/T]TTGGGATTTAATTAT | 22992 |
rs777950057 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67122740 | GAGTGCAGTGGCGCA[A/G]TCTCTGCTCACTGCA | 22992 |
rs777951522 | in-del | -/AAT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67137416 | TGGTTCAGGTAAGAC[-/AAT]GATGTGGTATGGTTG | 22992 |
rs777983089 | snp | C/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206539 | CTCAGGAGTTGGAGG[C/T]CATCCTGGGCAACAT | 22992 |
rs777992047 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67220125 | CAGTTGATCCTCCCA[C/G]CTCAGCCTCCCAGGT | 22992 |
rs778003097 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67152183 | CCAGGCGTGGTGGTG[C/T]GCACCTGTGCTTCCA | 22992 |
rs778005767 | snp | A/G | 1.92184e-05 | 0.00309981 | intron-variant | KDM2A | GRCh38.p7 | 11:67254168 | GGATTAGAGAATTGA[A/G]AGTTTTGATCTAGGC | 22992 |
rs778034346 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67122195 | TGACCTGAAAGGCCT[A/G]GAAGATTACTAAAGG | 22992 |
rs778074773 | snp | G/T | 2.60217e-05 | 0.00360696 | intron-variant | KDM2A | GRCh38.p7 | 11:67181312 | CTAATATTTTCCTAT[G/T]GTGACAGATTTTAAT | 22992 |
rs778094510 | snp | A/G | 3.31532e-05 | 0.0040713 | intron-variant | KDM2A | GRCh38.p7 | 11:67228210 | CACCGCTTAGGTCTG[A/G]GGGTGAGGCCCGAAA | 22992 |
rs778119053 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67204520 | TTTTTGAGACAGAGT[C/T]TCACTGTGTTGCCCA | 22992 |
rs778122880 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67244258 | AGTAGAAAACATGGT[C/G]CTTGTCCTTGAAAAG | 22992 |
rs778137853 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67215467 | TGATGCGCCCTGCAT[C/T]TTCCTCCGTGTGCTG | 22992 |
rs778140413 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67127680 | TCAGCAGCGATTACC[A/G]GATTATCTTTTTTAA | 22992 |
rs778158562 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67231972 | AAAGGTAAGGGTTTG[A/T]TGTGTTACATGACAG | 22992 |
rs778159665 | snp | C/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67120856 | TAATTTGGTTAGGAT[C/T]TGGATTAGTTCAGTG | 22992 |
rs778163107 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67229734 | AATTAGCCAGGCGTG[A/G]TGTTGCGCACCTGTA | 22992 |
rs778165672 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255216 | TGGGGCAGAGAGGGT[C/G]GTGGACACCAGGCTT | 22992 |
rs778177013 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67193367 | TGTCCTGTAAGGATA[A/G]TCATGTTCTCAGAAA | 22992 |
rs778178152 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67125303 | TTCCCACGTCAGCTT[C/T]CCAGGTAGCTAGGAC | 22992 |
rs778247209 | snp | A/G | | | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67246051 | AATGAAGAGACACAA[A/G]ACTTTGAGAAGAAAC | 22992 |
rs778249236 | snp | C/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67178100 | CTCATACCATACAGT[C/G]TCCTCATTTAAAGTG | 22992 |
rs778255147 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67191901 | AGTAAAGTCACCTCT[C/G]TTGGCAGATGATATG | 22992 |
rs778297642 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67143726 | CAACCTCTGCCTCCT[C/G]GGTTCTAGAGATTCT | 22992 |
rs778310942 | snp | C/T | 6.13346e-05 | 0.00553747 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255086 | GATTCAACAGGAAAC[C/T]GATCTTCCCCTGACT | 22992 |
rs778350678 | in-del | -/TCTCTCTT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67169759 | CTCTCTCTCTCTCTC[-/TCTCTCTT]TTTTTTTTTTTTTTT | 22992 |
rs778355959 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67221440 | ACAACTTTTATATGA[A/G]TGGTCTTTTATATAT | 22992 |
rs778395469 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67152777 | TCCATAGCAGATGTT[C/T]AATGATTTCAGTTCA | 22992 |
rs778406802 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67164593 | AAGCACTAGGATTAC[A/G]GGCATGAGCCATCAC | 22992 |
rs778419947 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67240731 | CTATCCCAAACCCCC[C/T]CTAGTGAAGGGTGGT | 22992 |
rs778435053 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67151125 | CCAATTATGCTGAAA[A/G]TACAGAACTGTTTCA | 22992 |
rs778438574 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255501 | TGTGGTGTCCAGTGC[A/G]CGTCTCTCCTCCATC | 22992 |
rs778446517 | in-del | -/C | 1.65776e-05 | 0.00287898 | intron-variant | KDM2A | GRCh38.p7 | 11:67228008 | TTCCTTGAAAATCGT[-/C]ATCTTTTCTCTATTT | 22992 |
rs778460624 | in-del | -/GTGTGTGTGTGTG | | | intron-variant | KDM2A | GRCh38.p7 | 11:67152940 | TGTGTGTGTGTGTGT[-/GTGTGTGTGTGTG]TTTTCAGGAATTCCT | 22992 |
rs778473310 | snp | C/G | 5.05872e-05 | 0.00502902 | intron-variant | KDM2A | GRCh38.p7 | 11:67245181 | ACCTCACTGCTTTCT[C/G]TTTCCAGCTTAAATT | 22992 |
rs778483788 | snp | C/T | 3.23661e-05 | 0.00402269 | intron-variant | KDM2A | GRCh38.p7 | 11:67181293 | AATTATACCACTTAT[C/T]TTTCTAATATTTTCC | 22992 |
rs778492079 | snp | C/G | 1.81477e-05 | 0.00301223 | synonymous-codon, intron-variant | KDM2A | GRCh38.p7 | 11:67250745 | TGTCTTCCGCTACCT[C/G]AGCCGCAGAGAACTT | 22992 |
rs778500088 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67159568 | TGCTGGTAGTGATGG[G/T]AAAAATTGATTAAGG | 22992 |
rs778513574 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67164249 | CATTTGTTCTTCTGA[-/T]TATGTAGTTTTGCTA | 22992 |
rs778528362 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67160171 | TTCCTGAAATAAAAT[G/T]CTATAGTTCAGTTCT | 22992 |
rs778548933 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67248110 | GAACCTGTGCCGCAC[C/T]GTCAAGATCAGGTTC | 22992 |
rs778564648 | snp | A/C | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67186143 | GAGTATAAACATCCA[A/C]ACAGCTCAATGAACT | 22992 |
rs778566902 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67202137 | AGAGAGCTAGAATTA[A/G]AAATGGAGTCGAAGA | 22992 |
rs778580050 | snp | C/T | 3.31246e-05 | 0.00406955 | synonymous-codon, nc-transcript-variant, intron-variant | KDM2A | GRCh38.p7 | 11:67243035 | GGAGCTTGCCAACAG[C/T]GATCCCAAGTTAGCC | 22992 |
rs778596211 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67136580 | GATGAGATACTTGTA[A/G]GATGGAGAATTCCTT | 22992 |
rs778609956 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67124139 | TTCCTGAGTAGCTGG[A/G]ACTACAGGTGCCCAC | 22992 |
rs778630590 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67137861 | GGAGTGCAGTGGTGC[A/G]ATCTCGGCTCACTGC | 22992 |
rs778635524 | snp | C/T | | | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67239997 | CAGAACGGCTGGGCC[C/T]TCTGCCTGGCTCGCT | 22992 |
rs778691122 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67223598 | ATTTTTTTGTAGAAA[C/T]GAGGTTTTACTATGC | 22992 |
rs778696566 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67192202 | TCCCTTTTCCTTCCT[C/T]CTCTCTCCAGAGATA | 22992 |
rs778707389 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67228711 | AAAAAAAAGAAAGAA[A/C]GAACGATGATCAGTT | 22992 |
rs778739453 | snp | C/T | | | | | GRCh38.p7 | 11:67208230 | AATTTTAAAATTTAT[C/T]ATTATTAAAAAAATT | 22992 |
rs778758911 | snp | C/T | 1.74756e-05 | 0.00295593 | | | GRCh38.p7 | 11:67217770 | GCCCACAACCTGGAG[C/T]TGTACGAGAATTGGC | 22992 |
rs778775763 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67213618 | ACAAAAATTAGTTAG[A/G]TGCGGTGGCGGGTGC | 22992 |
rs778779310 | in-del | -/TGTG | | | intron-variant | KDM2A | GRCh38.p7 | 11:67242279 | CTGTGGGTGTGTGTA[-/TGTG]TGTGTGTGTGTGTGT | 22992 |
rs778784709 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67162873 | CATGTGCCACCTTGC[A/C]CAGCTAATTTAATAA | 22992 |
rs778822781 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67235809 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 22992 |
rs778824840 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67183493 | ACTTTTCTCCTTACC[C/T]AGACAATAATTGCAC | 22992 |
rs778834324 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67251516 | CTCTAGGATATATCC[-/T]TTTTATCTGGGTCAC | 22992 |
rs778843637 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67194752 | ACAACCTGCTCTTGG[C/T]CTTTATCTCAGCAAG | 22992 |
rs778881235 | snp | C/G/T | 3.40996e-05 | 0.00412902 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67254204 | TCTTGCCTGTACAGG[C/G/T]CAGGACAATCGCAGC | 22992 |
rs778882605 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67161268 | GGCTGTGATGACAGC[A/T]TGATCATGGTAAACT | 22992 |
rs778926155 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67211825 | CATAATCTGTTTGTT[C/T]CCTGTGATCTTCACA | 22992 |
rs778966665 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67144772 | GGTTTCTCCATGTTA[C/T]CCAGGTTGGTCTTGA | 22992 |
rs779012037 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67209810 | TCATGCCTGTAATTC[C/T]AGCACTTTGGGAGGC | 22992 |
rs779035152 | snp | A/C | | | upstream-variant-2KB, utr-variant-3-prime | KDM2A, LOC107984341 | GRCh38.p7 | 11:67117287 | GAGTAATTATGCAAG[A/C]TCTTTAACCTTTCTA | 22992 |
rs779061012 | snp | A/G | 1.67478e-05 | 0.00289372 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67250306 | ATGAGCGCTTCAAAC[A/G]GCGGCAGTTGCTGCG | 22992 |
rs779077110 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67132656 | TCTCCAGTTTCAGGT[C/T]GGGGTGGTCTAGAAA | 22992 |
rs779120035 | snp | C/G | 1.81999e-05 | 0.00301655 | intron-variant | KDM2A | GRCh38.p7 | 11:67231997 | TGACAGCTACTGATC[C/G]AGCTATGGCAGTCAG | 22992 |
rs779124889 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67236643 | CTGCCAATCATACTT[G/T]GTGACTTTTGGGTAA | 22992 |
rs779127298 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67167190 | CAAGAATGTGCCTTA[A/G]ATATAACATCTAAAC | 22992 |
rs779138795 | snp | C/T | | | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67180126 | TGGCATTTCAGATGA[C/T]GAAATTGAAGGAAAA | 22992 |
rs779170228 | snp | C/T | 1.65611e-05 | 0.00287755 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67253529 | CAGCTGCCCCCTTCT[C/T]AGGACCCTTGATCTT | 22992 |
rs779176395 | snp | C/G | 1.65688e-05 | 0.00287821 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67246114 | CATCCTGGCTGCCTC[C/G]AGGTGAGGAGAGCTA | 22992 |
rs779192965 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67156493 | GGAGGCGAGGTGGGC[A/G]GATCACGAGGTCAGG | 22992 |
rs779208233 | snp | G/T | 1.68255e-05 | 0.00290043 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67207511 | ATCTTTTATGGCAGG[G/T]AGTCGTCGCATGGTG | 22992 |
rs779210761 | in-del | -/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67188159 | ACTGTAGTCCAGCCT[-/G]GGTGACAGAGCCAAG | 22992 |
rs779252422 | snp | C/T | 1.65608e-05 | 0.00287752 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67228066 | TCGCTATCCATTCTA[C/T]TATGAGATGTGTTGG | 22992 |
rs779266193 | snp | C/T | 3.24828e-05 | 0.00402993 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67248357 | ACCAGGAGGACAGCT[C/T]GGAGAAAGCCCAGGT | 22992 |
rs779271361 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67204594 | CCTCCTGGGTTCATG[C/T]CATTCTCCTGCCTCA | 22992 |
rs779284170 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67242777 | GCATGAGCCACTGTG[C/T]CCAGCCTCAAAGTTT | 22992 |
rs779289439 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67243970 | TGATAGCATTCTGAT[C/T]CTGGCTGTGAATTTG | 22992 |
rs779308036 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67133397 | GTGAGCCACCGTGCC[C/T]GGCCTATTTTTATTT | 22992 |
rs779315020 | in-del | -/ATT | 1.71196e-05 | 0.00292567 | intron-variant | KDM2A | GRCh38.p7 | 11:67254852 | TATGTGAGCACTGTC[-/ATT]ATGTCCACTTTCCCG | 22992 |
rs779318548 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67151699 | TTAAAATAGCCCCAT[A/G]ATTTTTTACATTGAC | 22992 |
rs779321831 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67140857 | GGTCTACTTTATGAA[A/G]AACCTTACCAGAGAT | 22992 |
rs779340255 | snp | C/T | 3.31934e-05 | 0.00407377 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67180119 | AAGATGATGGCATTT[C/T]AGATGATGAAATTGA | 22992 |
rs779391673 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67139819 | GGTTCAAGTGATTCT[C/T]CTGCCTCAGGTCCTG | 22992 |
rs779479977 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67127533 | TTATCGCATGTTCAA[C/T]CCTGTTAACCTGTCT | 22992 |
rs779493621 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67137280 | CCTGAAGCCATTGGG[-/A]AGGCAGAAGTTCAGC | 22992 |
rs779507500 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67145282 | CTGAGGTCAGGAGTT[C/T]GAGACCAGTCTGGCC | 22992 |
rs779515945 | in-del | -/TTTT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67134490 | CATTTTATAATTTTA[-/TTTT]TTAAAGTTTTATTTA | 22992 |
rs779524958 | snp | A/G | 7.67273e-05 | 0.00619337 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255066 | GCTAAGACACACCCA[A/G]CCCAGATTCAACAGG | 22992 |
rs779540997 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67170115 | AATATAGGAAGTGAG[A/G]ACACATTTTCATGGC | 22992 |
rs779548729 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67128704 | TGTTGTTTTATTTTG[C/G]TGAGCATTAATCACT | 22992 |
rs779582839 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67213428 | GTAAAATGTTGCGTA[C/T]TGCTTTCACTTCTCT | 22992 |
rs779584477 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67231375 | GTCCTCCTAGGTCAG[A/G]ATCCTGTTTCTACCT | 22992 |
rs779619905 | snp | A/C/T | 0.000111833 | 0.00747701 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255078 | CCAGCCCAGATTCAA[A/C/T]AGGAAACCGATCTTC | 22992 |
rs779620599 | snp | C/T | 1.67846e-05 | 0.0028969 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67254931 | GCATTGCCAACGTCA[C/T]CTTGATCGACCTTCG | 22992 |
rs779631862 | snp | C/T | 1.71032e-05 | 0.00292426 | missense, intron-variant | KDM2A | GRCh38.p7 | 11:67250569 | GCCCGAACCCCCCAG[C/T]GTGGGGATGAGGAGG | 22992 |
rs779634537 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67136184 | GGCATTTTCGATATA[C/G]TCACTAATTTAATTC | 22992 |
rs779698324 | snp | A/G | 4.97393e-05 | 0.0049867 | intron-variant | KDM2A | GRCh38.p7 | 11:67228006 | CTTTCCTTGAAAATC[A/G]TCATCTTTTCTCTAT | 22992 |
rs779699788 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67215210 | GCCAACAGATTTTTT[A/T]AATTTGCTTATAATT | 22992 |
rs779700263 | snp | C/T | 3.31802e-05 | 0.00407296 | intron-variant | KDM2A | GRCh38.p7 | 11:67121379 | TATTTTCTCCCCCCA[C/T]CACACCCTCCAGTTT | 22992 |
rs779722066 | snp | C/T | 1.80487e-05 | 0.00300401 | synonymous-codon, intron-variant | KDM2A | GRCh38.p7 | 11:67250730 | GGAGGTCTGGATGTC[C/T]GTCTTCCGCTACCTC | 22992 |
rs779759048 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67136245 | TCCCATTTTAAAGTT[G/T]TGGAAACAGATCCAA | 22992 |
rs779768853 | snp | A/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185915 | CCTCCAGAACTGTGA[A/G]CGAATAAATTTCTGT | 22992 |
rs779774909 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67151036 | TCTCCTTTGCTTGGA[C/G]GATATCATGGTGGAT | 22992 |
rs779777254 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67159027 | CAGTTTCATTGAAAT[A/C]CAGTTTATTAATTAT | 22992 |
rs779790225 | snp | A/G | 1.66021e-05 | 0.0028811 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67180095 | GTGGTACCATGCGAC[A/G]ACGCTATGAAGATGA | 22992 |
rs779826985 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67254544 | CTCATTTCTTCACAT[C/T]TGGACAAGGACATGG | 22992 |
rs779838752 | snp | A/C | 1.65781e-05 | 0.00287902 | intron-variant | KDM2A | GRCh38.p7 | 11:67243004 | CTTTTCCCTCCTACC[A/C]TTAGATTTTGCTGGA | 22992 |
rs779881812 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67134733 | TGGTCTCGAACTTCT[G/T]ACCTCAGGTGATCCA | 22992 |
rs779904896 | in-del | -/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67188326 | TCTCTACTAAAAATA[-/C]AAAATATTAGCCGGG | 22992 |
rs779905770 | snp | C/T | 1.65616e-05 | 0.00287759 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | KDM2A | GRCh38.p7 | 11:67215931 | CTCTGTTTGGTATCA[C/T]ATCCATCAAGGGGGA | 22992 |
rs779915018 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67253214 | TTTGAGCTCTTAGAA[A/G]GACAGGAAGTCACTC | 22992 |
rs779940415 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67144542 | CAGGTGTGAGCCACC[A/G]TGCCCGGCCCCAACA | 22992 |
rs779949840 | in-del | -/CCT | 8.77539e-05 | 0.00662339 | intron-variant | KDM2A | GRCh38.p7 | 11:67252593 | TTGTAGAAGAACGAG[-/CCT]CCTCCAGGTACTCTG | 22992 |
rs779951419 | snp | A/G | | | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67239656 | GAGAGAGAAGTGTGT[A/G]TGCAGTCAGCCAGAG | 22992 |
rs779963642 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67172489 | GTATATAAGTCTTGT[A/G]CTTATCTTGTTAAAT | 22992 |
rs780003406 | snp | C/G | 1.70769e-05 | 0.00292202 | missense, nc-transcript-variant, utr-variant-5-prime | KDM2A | GRCh38.p7 | 11:67215417 | ATCAACAAATGCCAT[C/G]TTGGAGATGCAGTAC | 22992 |
rs780008565 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67128309 | AAGTGTGAGCCACTG[C/T]GCCTGGACCCGTTCC | 22992 |
rs780011922 | snp | C/T | 1.9585e-05 | 0.00312924 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67231642 | CCGACGCTTGAGCAG[C/T]AGGCGTTCTGTCCTC | 22992 |
rs780050547 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67209249 | AAAGGAACTATTTTT[A/G]TATTAGTAATCATGT | 22992 |
rs780070204 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67243561 | GCTCACACCTGTAAT[C/G]CCAGCACTTTGGGAG | 22992 |
rs780095765 | in-del | -/TTT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67182531 | AAAATTGAATAAGTC[-/TTT]TTTTTTTTTTTTTTT | 22992 |
rs780102851 | snp | A/C | 1.65993e-05 | 0.00288086 | intron-variant | KDM2A | GRCh38.p7 | 11:67181841 | TACTGGTGTTTGTTT[A/C]ATAGAATGCCGGATC | 22992 |
rs780141861 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67234073 | AGAAGACAACAGATT[C/T]AGATTCCAGCTCTGC | 22992 |
rs780148902 | in-del | -/ACCAAA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67189360 | AACACAACACAGCCT[-/ACCAAA]ACTTATAGGGATCAG | 22992 |
rs780157673 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67177190 | AGAATCACTTGAACC[C/T]GGGAGGTGGAGGTTG | 22992 |
rs780158849 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67193626 | GGCACTTTGGGAGGC[C/T]GAGGCAGACAGATCA | 22992 |
rs780181148 | in-del | -/TG | | | downstream-variant-500B | KDM2A | GRCh38.p7 | 11:67258454 | TGTCCAGCTAATTTG[-/TG]TGTGTGTGTGTGTGT | 22992 |
rs780209256 | snp | A/G | 3.43932e-05 | 0.00414674 | intron-variant | KDM2A | GRCh38.p7 | 11:67254199 | TCTTCTCTTGCCTGT[A/G]CAGGTCAGGACAATC | 22992 |
rs780214487 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67144251 | GCCCTTGGCCTTAAA[-/T]TTTTTTTTTTTTTTT | 22992 |
rs780225034 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67217240 | GAGTGAAACTCTGTC[-/A]AAAAAAAAAAAAAAA | 22992 |
rs780284629 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67194612 | ACATAGGCACCCAAT[A/G]CATATTGGTGATTGC | 22992 |
rs780285951 | snp | G/T | 1.67775e-05 | 0.00289629 | intron-variant | KDM2A | GRCh38.p7 | 11:67253403 | TCGTTACGGCTCTGA[G/T]TATGCTGGGAAACAG | 22992 |
rs780286698 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67179892 | CCAGTGGCTCATTGA[A/G]ACTTCATTATATTCT | 22992 |
rs780295743 | snp | A/G | 1.65781e-05 | 0.00287902 | synonymous-codon, intron-variant | KDM2A | GRCh38.p7 | 11:67250403 | GTCTGAAGTTGAGAA[A/G]GCCAAGATCCGGGGA | 22992 |
rs780306672 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67235669 | CTCTGTCACCTAGGC[C/T]GGGGTGCAGTGGCGC | 22992 |
rs780311719 | in-del | -/GGTC | | | intron-variant | KDM2A | GRCh38.p7 | 11:67208220 | AAATTTTAAAATTTT[-/GGTC]AAAATTTATTATTAT | 22992 |
rs780316444 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67227498 | CAGAACCGAAACTTT[C/G]ATTGTTTTGATGCTT | 22992 |
rs780350469 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67159956 | ATTGATTGCATAACA[A/G]TATGAACATATTTAA | 22992 |
rs780359260 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67189188 | AATATCAGTGGATTT[A/G]AAAAATAGATATCAA | 22992 |
rs780360457 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | KDM2A, LOC107984341 | GRCh38.p7 | 11:67118708 | GACGGGCAGCCTGGG[A/G]CCAAAGGCGGTTGAA | 22992 |
rs780388355 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67144865 | GCCATCGTGCCTGGA[G/T]TTTTATTTTTATTTA | 22992 |
rs780390651 | snp | A/G | 1.66554e-05 | 0.00288573 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67252804 | TCAGCCTTGACCTCA[A/G]TTGGACCAACATCTC | 22992 |
rs780394205 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67154790 | GTATGACCTTTTGTG[G/T]CTGGCTTTCACTTAG | 22992 |
rs780411984 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67216486 | ATGCTTCTGAATGCT[A/G]TATGAGAATGGAAAT | 22992 |
rs780419089 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67153415 | GCTCCCAAAGAATGA[A/G]GGAAATTTGGTTTAA | 22992 |
rs780442713 | in-del | -/AAG | | | intron-variant | KDM2A | GRCh38.p7 | 11:67243825 | TCTCAAAGAAAAAAA[-/AAG]AAGAAGAAGAAAGGA | 22992 |
rs780445732 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67231999 | ACAGCTACTGATCCA[A/G]CTATGGCAGTCAGCT | 22992 |
rs780460580 | in-del | -/G | 1.65817e-05 | 0.00287933 | intron-variant | KDM2A | GRCh38.p7 | 11:67246133 | TGAGGAGAGCTATGA[-/G]GGGTTCCTGAAGTCT | 22992 |
rs780515907 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67242627 | TACACAAGTAAGGGA[C/T]TGGGAACAAAGGTGA | 22992 |
rs780550425 | in-del | -/TGATCAGTAAACCAGAA | 7.37055e-05 | 0.0060702 | intron-variant | KDM2A | GRCh38.p7 | 11:67254480 | GCCCTCCCTGGAACT[-/TGATCAGTAAACCAGAA]TGACCTTGGGTCTGT | 22992 |
rs780608233 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67217128 | ACGCCTGTAGTCCCA[G/T]CAACTCTGGAGGCTG | 22992 |
rs780627012 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67175730 | AGAAGAATCCGTTAT[A/G]GTAGACCTAATAAAA | 22992 |
rs780644859 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67205240 | CAGTTTTGATTTGAC[A/G]TTCACTTTTTCTTTT | 22992 |
rs780666602 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67196814 | CACAACATTGTGAAT[A/G]TATTTAATAACACTG | 22992 |
rs780688409 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67251300 | TAACATTTTTCTTCA[A/G]TTTTAATGCTCATCC | 22992 |
rs780706922 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67213297 | ACCATAAGTTAGATA[G/T]TTACCACATCAGCAC | 22992 |
rs780721896 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67177033 | GAGGCTGAGGTGGGC[A/G]GATCACCTGAGGTCA | 22992 |
rs780727557 | snp | A/C | 1.65842e-05 | 0.00287955 | intron-variant | KDM2A | GRCh38.p7 | 11:67121365 | CAGAGATTGGTTAGT[A/C]TTTTCTCCCCCCACC | 22992 |
rs780747419 | snp | C/T | 1.86939e-05 | 0.00305722 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | KDM2A | GRCh38.p7 | 11:67219310 | TCATGCTGTGTATAC[C/T]CCTACAGACACATTA | 22992 |
rs780770391 | snp | C/T | 4.97228e-05 | 0.00498587 | missense, intron-variant | KDM2A | GRCh38.p7 | 11:67250435 | CGTACCTCACTGTCA[C/T]GCTACAGAGGCCCAC | 22992 |
rs780798181 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67133379 | AGGGCTGGGATTATA[C/G]GTGTGAGCCACCGTG | 22992 |
rs780798345 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67169404 | TTTTTTTTGAGATGA[A/C]GTTTCGCTCCTGTTG | 22992 |
rs780799841 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67162722 | GCGATTTTTAGTTTT[A/G]TTTTTTTCCTAGACA | 22992 |
rs780805760 | snp | C/G | 1.66275e-05 | 0.00288331 | intron-variant | KDM2A | GRCh38.p7 | 11:67254526 | TTGATTGACCCACAT[C/G]AGCTCATTTCTTCAC | 22992 |
rs780813737 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67190138 | GTGAGGGCCGAGCGC[A/G]GTGGCTGACACCTAT | 22992 |
rs780834905 | snp | A/C | 4.97187e-05 | 0.00498567 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67245988 | GTCCTCTTGTAGCCC[A/C]GACTGCCTCACTCAG | 22992 |
rs780835256 | snp | C/G | 1.90239e-05 | 0.00308408 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | KDM2A | GRCh38.p7 | 11:67217844 | ATCAGATTGTCAGCG[C/G]ATTGAGCTCAAGCAG | 22992 |
rs780853482 | in-del | -/CT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67167069 | GGCGACAGAGCGAGA[-/CT]CTGCCTCAAAAAAAA | 22992 |
rs780897342 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67196473 | GCTAAAATGTAGCAA[C/T]CTAAATGTCCATCAG | 22992 |
rs780902998 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67198074 | TCTTTTCATCTTCAT[A/G]ATGAGTAGGCTAAGG | 22992 |
rs780910065 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67149208 | GGGCTATAACCTGGT[G/T]TTGGTGGAGTCCCTT | 22992 |
rs780923273 | snp | A/G | 2.64778e-05 | 0.00363843 | intron-variant | KDM2A | GRCh38.p7 | 11:67219272 | CAGCCACTGCCCTCT[A/G]TTCCCCTTCTCCTAG | 22992 |
rs780927696 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67257067 | TTCTTTGGTTGCTCC[C/T]GTGGAAAATACTGAA | 22992 |
rs780945952 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67170383 | TTATCCTACCAAGCA[-/T]GGGGTTTTTTTTTTT | 22992 |
rs780975839 | snp | C/T | 1.69381e-05 | 0.00291011 | synonymous-codon, intron-variant | KDM2A | GRCh38.p7 | 11:67250556 | GCAGCACTGCCCAGC[C/T]CGAACCCCCCAGCGT | 22992 |
rs780992130 | in-del | -/AT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67183685 | GACAAGCAGCTGTGC[-/AT]ATGTTTCCCCGAAAA | 22992 |
rs781005975 | snp | C/G | 1.68278e-05 | 0.00290062 | intron-variant | KDM2A | GRCh38.p7 | 11:67180058 | TGCATGATTTCATCA[C/G]TATGTTCCTTTCTTT | 22992 |
rs781015075 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67127512 | GAGCTTTTCTAAAAG[A/G]TGTTATTATCGCATG | 22992 |
rs781018110 | in-del | -/TTAAG | | | intron-variant | KDM2A | GRCh38.p7 | 11:67152803 | GTTCAGTAAGAATAT[-/TTAAG]TTATTTAACTTTTGT | 22992 |
rs781033011 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67164388 | TCTGGAGAAGTTTAA[C/T]AGAGATGTGATTATT | 22992 |
rs781040028 | snp | C/T | 1.66078e-05 | 0.00288161 | intron-variant | KDM2A | GRCh38.p7 | 11:67242992 | TGATTTTTCCTTCTT[C/T]TCCCTCCTACCCTTA | 22992 |
rs781084427 | snp | G/T | 0.000106294 | 0.00728944 | intron-variant | KDM2A | GRCh38.p7 | 11:67252892 | GCTGTCTTTCCAGGG[G/T]CCCAGAAGAAGCGGG | 22992 |
rs781085297 | in-del | -/TGT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67167230 | TTCTCTTCAAGATGA[-/TGT]TGAGATGCCTTATCC | 22992 |
rs781131777 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67122407 | TCTGAGCTCACCGCA[C/G]CCTCCACCTCCTGGG | 22992 |
rs781142025 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67125964 | AAAAAAAAAAAAAAA[G/T]GCCAGGCACAGTGTC | 22992 |
rs781144216 | snp | C/T | 1.68516e-05 | 0.00290268 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67250193 | TCATTCACCCACTTC[C/T]ATGCTGCAGCTCATC | 22992 |
rs781219846 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67171075 | GCATAGTGCTTGTTA[C/T]AGTACCTGGCACATG | 22992 |
rs781224845 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67134688 | TTTTATATTTTTAGT[G/T]GAGACAGGATTTCGC | 22992 |
rs781239345 | snp | C/G | 0.000441276 | 0.0148473 | missense, nc-transcript-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67207515 | TTTATGGCAGGGAGT[C/G]GTCGCATGGTGGATG | 22992 |
rs781296382 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67192158 | TGTTAGCATTGACAT[A/C]CACTGTGTACCATTC | 22992 |
rs781297744 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67205006 | CTTGTTCAATTCTTT[C/T]AGATATATGCCTAGA | 22992 |
rs781304006 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67225170 | TGCCACGAACTATCT[C/T]GCTTTTATTATTTTC | 22992 |
rs781328830 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67193506 | AAAGTTAATACACAT[A/G]AAGTGCTCAGAAGAG | 22992 |
rs781334528 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67156847 | TGAGCCGAGATCGCG[C/T]CACTGCACTTCATCC | 22992 |
rs781382260 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67181511 | ATTGAAAATAATTTC[C/T]CACTTTGTTTTAAAA | 22992 |
rs781411056 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67176892 | AATAGTGAGTAAATG[C/G]GAGGGCCTAAGACAC | 22992 |
rs781434603 | snp | A/G | 3.33968e-05 | 0.00408623 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67250297 | CCAGCCGCGATGAGC[A/G]CTTCAAACGGCGGCA | 22992 |
rs781471844 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67130829 | TAATTCTCAAAACAA[C/T]CCTGGAAGGTAGATG | 22992 |
rs781504977 | snp | C/G | 1.66192e-05 | 0.00288259 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67252755 | AAGGCCATTGTGCCC[C/G]AGGCCCTCAGTGGCA | 22992 |
rs781515026 | in-del | -/TTTA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67191922 | AGATGATATGACTTT[-/TTTA]TTTGTTATTAGTATT | 22992 |
rs781524538 | snp | G/T | 2.08479e-05 | 0.00322855 | missense, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67231632 | ATCGAGAACCCCGAC[G/T]CTTGAGCAGCAGGCG | 22992 |
rs781530899 | snp | A/G | 0.000216951 | 0.0104129 | intron-variant | KDM2A | GRCh38.p7 | 11:67181819 | AATTGTGTTTTCCAT[A/G]TATACTTACTGGTGT | 22992 |
rs781540490 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67248106 | ATCAGAACCTGTGCC[A/G]CACTGTCAAGATCAG | 22992 |
rs781552509 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67232213 | AACATAGGTTTCAGG[C/G]TGACCCCAAAAATAA | 22992 |
rs781564422 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67216296 | TAGTGGAAGGGAACA[A/C]GAATTTTGGATAGAT | 22992 |
rs781577665 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67165935 | TACTTTCATTAATCC[A/T]TATATTCTAGGAACT | 22992 |
rs781592335 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67128957 | ATGCAGTGGCTCTCA[C/G]CTGTGGTCCCAGCTA | 22992 |
rs781626042 | snp | C/G | 5.60428e-05 | 0.00529323 | intron-variant | KDM2A | GRCh38.p7 | 11:67252615 | GGTACTCTGCTTTTC[C/G]CAGAAGCCATAAGCA | 22992 |
rs781649335 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67215566 | AAAAAGATGAATTAT[C/T]TAAAGATGAGACTTT | 22992 |
rs781654030 | snp | C/G | | | upstream-variant-2KB, utr-variant-3-prime | KDM2A, LOC107984341 | GRCh38.p7 | 11:67117653 | AGAGTGGGAAACCAA[C/G]GCAGGGAGAAAAAGA | 22992 |
rs781654914 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67234000 | TGAATTCTCCCTCCA[A/G]AGACTTGTCCACAGC | 22992 |
rs781683286 | in-del | -/G | 4.97657e-05 | 0.00498802 | intron-variant | KDM2A | GRCh38.p7 | 11:67121377 | GTATTTTCTCCCCCC[-/G]ACCACACCCTCCAGT | 22992 |
rs781714054 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67254817 | GCTACAGGAATTGAA[C/T]GGCAGAGGAAAGCTG | 22992 |
rs781758841 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67151681 | CTTGGTATGAAAAAA[A/G]GATTAAAATAGCCCC | 22992 |
rs781780029 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67188896 | ATTTATGTACCTAAC[A/G]ACAGACCATCAGTAT | 22992 |
rs796069694 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67167318 | TCATAGTTAAATGTG[C/T]AGCAAGCACACTGAA | 22992 |
rs796078248 | snp | C/G | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185569 | CGGGAGGTGGAGGTT[C/G]CAGTGAGACAAGGTC | 22992 |
rs796152419 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67216147 | TCTAGTTCACTGTCA[C/T]TACACCATTGGCACA | 22992 |
rs796219038 | in-del | -/TATAT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67141684 | AAAAAAAAAAAAAAA[-/TATAT]ATATATATATATATA | 22992 |
rs796237196 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67190208 | TGAGGTGAGGAGTTC[A/G]AGACTAGCCTGGCCA | 22992 |
rs796269059 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67202068 | CTTATTGATGACTTT[A/G]AGGGGTTCAAGACTT | 22992 |
rs796302137 | multinucleotide-polymorphism | AAA/CAG | | | intron-variant | KDM2A | GRCh38.p7 | 11:67233500 | TACTAAAAATACAAA[AAA/CAG]TAGCTGGGTGTGGTG | 22992 |
rs796323697 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67141986 | TTCCATCCATGTTCC[A/G]AAAATGACAGAATTT | 22992 |
rs796336766 | in-del | -/AGAA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67253210 | GCATTTTGAGCTCTT[-/AGAA]AGACAGGAAGTCACT | 22992 |
rs796352269 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67147237 | CTCTGGGAATGGTCA[C/G]GTTAAAAGATATGAC | 22992 |
rs796361063 | multinucleotide-polymorphism | CA/TG | | | intron-variant | KDM2A | GRCh38.p7 | 11:67233544 | TAATCCCAGCTACTC[CA/TG]GAGGCTGAGGCAGGA | 22992 |
rs796387276 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67227058 | TCCTGGACTGTGATA[C/T]ATCTAAAGAGTACCT | 22992 |
rs796399563 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67167969 | ACAAAAAGTTTTATA[C/T]AGATCAAAAGATAAA | 22992 |
rs796405175 | multinucleotide-polymorphism | CA/TG | | | intron-variant | KDM2A | GRCh38.p7 | 11:67233508 | ATACAAAAATTAGCT[CA/TG]GTGTGGTGGCAGACA | 22992 |
rs796495559 | in-del | -/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67184786 | AAGACGTAAGAAAAC[-/T]TAAGTGTATACCTCA | 22992 |
rs796537969 | snp | C/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206862 | ATAGTTAACAAGAAT[C/T]TGATATAGATTTTCG | 22992 |
rs796555976 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67170388 | CTACCAAGCATGGGG[-/T]TTTTTTTTTTTCTTT | 22992 |
rs796562568 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67126859 | AGAATATTCTGCAGT[A/G]TTGGAGTGGAACAGC | 22992 |
rs796591373 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67251413 | TTAAGTTGGACAGAC[A/C]CTTGGGGGAAAAAAT | 22992 |
rs796593573 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67246920 | CATTAAGCATATGTT[A/G]AATGAAGAACCGGGT | 22992 |
rs796597184 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67169777 | TTTTTTTTTTTTTTG[A/G]GACGGAGTCTCACTC | 22992 |
rs796610346 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67153057 | TGGCACGATCTCAGC[C/T]CACTGCAACGTCTGC | 22992 |
rs796611566 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67223000 | GAAGTTGAGACCAGC[A/G]TGAGCAACATGAAGA | 22992 |
rs796627456 | multinucleotide-polymorphism | CA/TG | | | intron-variant | KDM2A | GRCh38.p7 | 11:67233512 | AAAAATTAGCTGGGT[CA/TG]GGTGGCAGACACCTG | 22992 |
rs796688619 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67198709 | GTGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 22992 |
rs796688890 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67180773 | TTCTCCTACCTCAGC[C/T]TCCTGAGTAGCTGGG | 22992 |
rs796722838 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67235816 | GTAGAGACGGGGTTT[C/T]ACCATGTTGGCCAGG | 22992 |
rs796776472 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67171246 | AGAGAGCTACTTGCC[A/G]ACCCCACCATCAGGT | 22992 |
rs796790993 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67128394 | TAAGCCTTTTTTTTT[-/T]CTAGTATGAAAGTAT | 22992 |
rs796825192 | in-del | -/TT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67197176 | TTATCAGAAATAAAC[-/TT]TTTTTTTTTTTTTTG | 22992 |
rs796879533 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67169048 | GCAACCTCTGCTGCC[A/G]GGGTTCAAGCGATTC | 22992 |
rs796891412 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67152014 | GGTTAAATAAAATAT[A/G]TTATTAAAATTAATT | 22992 |
rs796916214 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67253348 | ATTAGGCATAGTCCT[C/T]CTCTCCTATTAGACT | 22992 |
rs797013121 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67130925 | CATGACTTGCCCAAG[A/G]TCACAGAGTCGGTAA | 22992 |
rs797020173 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67162874 | ATGTGCCACCTTGCC[C/T]AGCTAATTTAATAAA | 22992 |