SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3624 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67213707 | tgtgggtgcgatctc[A/G]gctcactgcaacctc | 22992 |
rs608273 | snp | C/T | 0.453697 | 0.14494 | intron-variant | KDM2A | GRCh38.p7 | 11:67158297 | atgaactatgaaaca[C/T]ccatacaatgcaata | 22992 |
rs629570 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | KDM2A | GRCh38.p7 | 11:67183640 | CAGGGAAGAATGGAG[A/C]AGCTGTTACTGTGCT | 22992 |
rs645387 | snp | A/C | 0.103438 | 0.202533 | intron-variant | KDM2A | GRCh38.p7 | 11:67192921 | acaaaggacactctc[A/C]tacttgactcaacaa | 22992 |
rs646834 | snp | A/C | 0.458315 | 0.13822 | intron-variant | KDM2A | GRCh38.p7 | 11:67165282 | CATGCGCCGCCACAC[A/C]TGGCTAATTTTGTAT | 22992 |
rs655168 | snp | A/G | 0.101658 | 0.201233 | intron-variant | KDM2A | GRCh38.p7 | 11:67151807 | tagtaagctagataa[A/G]gccatactacactcc | 22992 |
rs660960 | snp | A/T | 0.455621 | 0.142197 | intron-variant | KDM2A | GRCh38.p7 | 11:67200126 | taacattttgaaagg[A/T]accttttttcctgag | 22992 |
rs662434 | snp | C/T | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67135079 | TTTCTTTTTTTTTTT[C/T]CCCCCTGAGACGGAG | 22992 |
rs674499 | snp | A/G | 0.453697 | 0.14494 | intron-variant | KDM2A | GRCh38.p7 | 11:67195954 | TTTGCCAAATCCACA[A/G]TATCTTCTATCAACT | 22992 |
rs681646 | snp | A/C | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67172345 | cttccaattcaaagc[A/C]attcttatcaaaatc | 22992 |
rs682105 | snp | A/C | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67172245 | cagaatagtcaaaac[A/C]atccttaaagaggac | 22992 |
rs682117 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67172232 | acaatccttaaagag[A/G]acaaaAGAAAGCTAg | 22992 |
rs682509 | snp | A/G | 0.103794 | 0.20279 | intron-variant | KDM2A | GRCh38.p7 | 11:67176383 | AATCTAGAATTTAAA[A/G]CTAAGTATTGATGAT | 22992 |
rs1253778 | snp | C/T | 0.459233 | 0.136827 | intron-variant | KDM2A | GRCh38.p7 | 11:67170537 | CCTGCCTGAGCCTCC[C/T]GAGTAGCTGGGACTG | 22992 |
rs1253784 | snp | A/C | 0.101658 | 0.201233 | intron-variant | KDM2A | GRCh38.p7 | 11:67165939 | TTCATTAATCCTTAT[A/C]TTCTAGGAACTAAAT | 22992 |
rs1253785 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67198646 | acccggaaggcggag[C/G]ttgcagtgagctgag | 22992 |
rs1253786 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67198665 | cagtgagctgagatc[A/C]cgccactgcactcca | 22992 |
rs1262158 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67198711 | tgagactctgtctca[A/G]aaaaaaaaaaaaaat | 22992 |
rs1269964 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67140715 | ccaagattgtgccat[C/T]gcactccagcctggc | 22992 |
rs1271742 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67173948 | gtaggaggatcactt[G/T]ctgaagccaggagct | 22992 |
rs1573537 | snp | C/T | 0.0155248 | 0.0867259 | missense, nc-transcript-variant, utr-variant-5-prime | KDM2A | GRCh38.p7 | 11:67215945 | TATGACCATACCTTT[C/T]CCCCTTGATGGATGT | 22992 |
rs1620695 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67143226 | ggggttggctggtct[C/T]gaactcgtgacctca | 22992 |
rs1944098 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67221033 | GGAGTGTTTTTTACC[C/T]TTTTTTTTTTTTTTC | 22992 |
rs1945571 | snp | A/C | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67238006 | TGTATGAATTATTAC[A/C]AATATCTTGTTAGTA | 22992 |
rs1945572 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67237969 | GCCAATAAAGTTTTA[A/T]TTGTATAAATAAATA | 22992 |
rs2156820 | snp | A/G | 0.0058823 | 0.0539124 | intron-variant | KDM2A | GRCh38.p7 | 11:67212833 | TCCTCTCCCTATTCA[A/G]ACATGGGAGCTTACA | 22992 |
rs2509809 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67204530 | cactccagcctgggc[A/G]acacagtgagactct | 22992 |
rs2509810 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67139262 | ttttcttttttcttt[G/T]gagacggagtctcgc | 22992 |
rs3741189 | snp | C/T | 0.0525783 | 0.153378 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67228132 | CCGTTCCCACCTAAC[C/T]AAGGAATTTCAGAAA | 22992 |
rs3825022 | snp | A/G | 0.119281 | 0.213102 | intron-variant | KDM2A | GRCh38.p7 | 11:67245726 | TCTTTCCCCTCTTCA[A/G]GTAGATTAGAAAGGA | 22992 |
rs3839938 | in-del | -/AT | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67257238 | TGGGTTTTGGTTTTT[-/AT]GTTTGTTTTTTGGGG | 22992 |
rs3892143 | snp | G/T | 0.0403638 | 0.136208 | intron-variant | KDM2A | GRCh38.p7 | 11:67254459 | CAGGGAGGGCTGGAG[G/T]CAGGGGGCACCGCTG | 22992 |
rs3892144 | snp | C/T | 0.0400407 | 0.13571 | intron-variant | KDM2A | GRCh38.p7 | 11:67254458 | AGGGAGGGCTGGAGG[C/T]AGGGGGCACCGCTGA | 22992 |
rs3892201 | snp | C/T | 0.00394476 | 0.0442359 | intron-variant | KDM2A | GRCh38.p7 | 11:67251538 | CTGGGTCACACACAT[C/T]CTATTACAGTagtgt | 22992 |
rs3927807 | snp | A/G | 0.454061 | 0.144427 | intron-variant | KDM2A | GRCh38.p7 | 11:67231384 | ACAGTTAACAGGTAG[A/G]AACAGGATCCTGACC | 22992 |
rs4072610 | snp | C/T | | | upstream-variant-2KB, synonymous-codon | KDM2A, LOC107984341 | GRCh38.p7 | 11:67118188 | GAGGAGCGGGGGCTT[C/T]CTGGGCCACCTcgcc | 22992 |
rs4084237 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67256390 | TAAAAATATTGACCC[A/C]AAAGAAATTCCGACC | 22992 |
rs4084238 | snp | C/T | 0.118584 | 0.212673 | intron-variant | KDM2A | GRCh38.p7 | 11:67234637 | GCTTTAGGCGGCAGA[C/T]GCAGGCAGATCTCTT | 22992 |
rs4244819 | snp | C/T | 0.456095 | 0.141508 | intron-variant | KDM2A | GRCh38.p7 | 11:67121828 | TTTTATAAATTAACA[C/T]TTTGGTAGCTTTGAA | 22992 |
rs4271388 | snp | C/T | 0.10237 | 0.201756 | intron-variant | KDM2A | GRCh38.p7 | 11:67202952 | gctggagtgcactgg[C/T]gcaatcacagctcac | 22992 |
rs4344498 | snp | A/G | 0.103438 | 0.202533 | intron-variant | KDM2A | GRCh38.p7 | 11:67226792 | taaaattaaatgagc[A/G]ctggccgcgagctgc | 22992 |
rs4375446 | snp | C/T | 0.453331 | 0.145452 | intron-variant | KDM2A | GRCh38.p7 | 11:67143355 | TTTGCTACAGGACTT[C/T]AGGAGCACTAGCATC | 22992 |
rs4385901 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67163816 | caggctggagtacag[A/G/T]ggtgctatctcggct | 22992 |
rs4457752 | snp | A/C | 0.10237 | 0.201756 | intron-variant | KDM2A | GRCh38.p7 | 11:67203325 | attgcaataaagcaa[A/C]tattccagtaagcaa | 22992 |
rs4478996 | snp | A/G | 0.453697 | 0.14494 | intron-variant | KDM2A | GRCh38.p7 | 11:67122087 | AAGAGAGCTTTATTA[A/G]TAGTCTCACAGTATT | 22992 |
rs4489751 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67136553 | CATCATCCTTGTAAT[G/T]TCTTCAAAGCACTCA | 22992 |
rs4503557 | snp | A/G | 0.455621 | 0.142197 | intron-variant | KDM2A | GRCh38.p7 | 11:67217040 | taaggtcaggagatc[A/G]agaacatcttggcca | 22992 |
rs4542419 | snp | C/T | 0.455263 | 0.142713 | intron-variant | KDM2A | GRCh38.p7 | 11:67203126 | ggcctgtggaggaac[C/T]tgcctcattgttgag | 22992 |
rs4930190 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | KDM2A | GRCh38.p7 | 11:67213545 | ggtggattgcctgag[A/G]tcagaagttcgagac | 22992 |
rs4930413 | snp | G/T | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67137497 | tgattgattctatga[G/T]aactatatatgaaat | 22992 |
rs4930414 | snp | A/G | 0.122411 | 0.214991 | intron-variant | KDM2A | GRCh38.p7 | 11:67171282 | TCAGTGTTCCTAGTC[A/G]GGACAGACGAGGCCG | 22992 |
rs4930415 | snp | A/G | 0.119978 | 0.213528 | intron-variant | KDM2A | GRCh38.p7 | 11:67215670 | CATTTTAGTCAATAC[A/G]GTAGAAAAAAAAAAA | 22992 |
rs6591232 | snp | A/G | 0.453939 | 0.144598 | intron-variant | KDM2A | GRCh38.p7 | 11:67153033 | CTTTCTGCCCAGGCT[A/G]GAGTGAAATGGCACG | 22992 |
rs6591234 | snp | A/G | 0.236144 | 0.249616 | intron-variant | KDM2A | GRCh38.p7 | 11:67176401 | TAAATTCTAGATTTG[A/G]TGTTCTTAGCACAGA | 22992 |
rs6591235 | snp | C/T | 0.236144 | 0.249616 | intron-variant | KDM2A | GRCh38.p7 | 11:67182903 | AAATTTTCTTCCTAG[C/T]ACTAGAATTTCTATT | 22992 |
rs6591238 | snp | C/G/T | 0.00953873 | 0.0683987 | intron-variant | KDM2A | GRCh38.p7 | 11:67221988 | GTAAATATTCTAAAA[C/G/T]AGGGAAAATGTTTCA | 22992 |
rs6591239 | snp | G/T | 0.456214 | 0.141336 | intron-variant | KDM2A | GRCh38.p7 | 11:67224146 | TTTTTGAAAAGGGAC[G/T]CCTATCCAGTTCTCC | 22992 |
rs7102849 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67151539 | atttttagtagagac[C/T]ggggtttcaccatgt | 22992 |
rs7104726 | snp | A/G | 0.167809 | 0.236103 | intron-variant | KDM2A | GRCh38.p7 | 11:67192506 | ctggagtgcagtggc[A/G]tgatcttggctcact | 22992 |
rs7104783 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | KDM2A | GRCh38.p7 | 11:67192734 | acaggcatgagccac[C/T]gtgcctggcctccat | 22992 |
rs7107527 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67233499 | tctactaaaaataca[A/T]aaattagctgggtgt | 22992 |
rs7107542 | snp | A/G | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67233532 | TGGCAGACACCTGTA[A/G]TCCCAGCTACTCAGG | 22992 |
rs7109019 | snp | G/T | | | upstream-variant-2KB, synonymous-codon | KDM2A, LOC107984341 | GRCh38.p7 | 11:67118008 | GGAGACATCTTcccg[G/T]ccgggcctcccgcgc | 22992 |
rs7109273 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67230943 | AGACAAAAAAAAAAA[A/G]ttttttggttttttt | 22992 |
rs7113390 | snp | C/T | 0.455858 | 0.141853 | intron-variant | KDM2A | GRCh38.p7 | 11:67224761 | ttgagctatcttgtc[C/T]ggccaaaattaatcc | 22992 |
rs7115659 | snp | C/G | 0.175576 | 0.238665 | intron-variant | KDM2A | GRCh38.p7 | 11:67152898 | GACTATAGGATTACA[C/G]TGCCAGAgtgtgtgt | 22992 |
rs7123691 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | KDM2A | GRCh38.p7 | 11:67242571 | GAAGTAACACTTGTC[A/G]CCACAGTAAGTTAGT | 22992 |
rs7124968 | snp | A/G | 0.499218 | 0.0197529 | intron-variant | KDM2A | GRCh38.p7 | 11:67202682 | tcaggaggctgaggc[A/G]ggagaatggcgtgaa | 22992 |
rs7125190 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67230944 | GACAAAAAAAAAAAG[G/T]tttttggtttttttt | 22992 |
rs7478885 | snp | C/G/T | 0.174801 | 0.238964 | intron-variant | KDM2A | GRCh38.p7 | 11:67211421 | gagttcaaaaccagc[C/G/T]tggccaacatggtga | 22992 |
rs7928575 | snp | C/T | 0.175576 | 0.238665 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67178371 | agtggagccactgca[C/T]tccagcctgcgcgac | 22992 |
rs7930094 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67145283 | tgaggtcaggagttc[A/G]agaccagtctggcca | 22992 |
rs7930829 | snp | C/G | 0.456332 | 0.141164 | intron-variant | KDM2A | GRCh38.p7 | 11:67145937 | GGAGATTTTCAACAT[C/G]TTTCTCTGTTTCTGG | 22992 |
rs7931772 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | KDM2A | GRCh38.p7 | 11:67133654 | gtgatctgcccacct[C/T]ggcctcccaaagtgc | 22992 |
rs7935423 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | KDM2A | GRCh38.p7 | 11:67171760 | tggcctcaagtgatc[C/G]tcgtgccttggcctc | 22992 |
rs7938349 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67147839 | cctgccaccacaccc[A/G]gctaattttttgtat | 22992 |
rs7938436 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67147812 | ccttccaagtagctg[C/G]gattacaggcgcctg | 22992 |
rs7938717 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67147851 | cccagctaatttttt[G/T]tatttttagtagaga | 22992 |
rs7945629 | snp | A/G | 0.161596 | 0.233848 | intron-variant | KDM2A | GRCh38.p7 | 11:67154879 | gctgaataatattcc[A/G]ttgtatggatatacc | 22992 |
rs7948579 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67247073 | tatatatatatatat[A/T]tTTtttttttttttt | 22992 |
rs7949844 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | KDM2A | GRCh38.p7 | 11:67210260 | ccagctactcagggg[A/G]ttgaggcaggaggat | 22992 |
rs7950442 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | KDM2A | GRCh38.p7 | 11:67173552 | gtgagccaccatgcc[C/T]agccAGtttttgtat | 22992 |
rs7952436 | snp | C/T | 0.0387552 | 0.1337 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67257063 | CTTTTTCTTTGGTTG[C/T]TCCTGTGGAAAATAC | 22992 |
rs9630209 | snp | A/C | 0.234692 | 0.249531 | intron-variant | KDM2A | GRCh38.p7 | 11:67254047 | AGAAACTGCCTACAC[A/C]CAGTGCTCACACCCT | 22992 |
rs9943601 | snp | A/G | 0.452965 | 0.145963 | intron-variant | KDM2A | GRCh38.p7 | 11:67142661 | gtgagccgagattgc[A/G]ccatcgcactccaga | 22992 |
rs10128545 | snp | C/T | 0.161596 | 0.233848 | intron-variant | KDM2A | GRCh38.p7 | 11:67182158 | TGCCTTCTAGGGCAA[C/T]CTTTCCAAGAAACCG | 22992 |
rs10219364 | snp | A/C | 0.365024 | 0.221967 | intron-variant | KDM2A | GRCh38.p7 | 11:67157332 | CAAAAAAAAAAAAAA[A/C]AAAAAACACCACACA | 22992 |
rs10400320 | snp | G/T | 0.113685 | 0.209567 | intron-variant | KDM2A | GRCh38.p7 | 11:67169549 | catacctggctaatt[G/T]ttttttggtagagaa | 22992 |
rs10542275 | in-del | -/TTAT | 0.247905 | 0.249991 | intron-variant | KDM2A | GRCh38.p7 | 11:67223389 | TTCCTTTTTTCTTTC[-/TTAT]TTATTTATTTATTTA | 22992 |
rs10585037 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67171492 | AAGTTGAGATCTGAG[-/A]GGTTAAATGATTTAT | 22992 |
rs10732253 | snp | C/T | 0.103794 | 0.20279 | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67238929 | GAGTGTGCACCCTCC[C/T]TTCCTCCTGTAGACT | 22992 |
rs10750796 | snp | A/C | 0.104504 | 0.2033 | intron-variant | KDM2A | GRCh38.p7 | 11:67224958 | ACAATTCTCCTGCCC[A/C]GGCATCCCGAGTAGC | 22992 |
rs10791900 | snp | A/T | 0.213937 | 0.247385 | intron-variant | KDM2A | GRCh38.p7 | 11:67153824 | GTCTCAAAAAAAAAA[A/T]AAAAAACACCAAAAA | 22992 |
rs10896158 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67170599 | tttgtatttttagta[A/G]aaacggggtttcacc | 22992 |
rs10896160 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67203464 | AATTATATTTATTAA[C/T]TATTAATAATTATTA | 22992 |
rs10896161 | snp | A/G | 0.238171 | 0.24972 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67205687 | GTGTTTTGCTATGTT[A/G]CCCAGGCTGGTCTCA | 22992 |
rs10896162 | snp | G/T | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67211710 | AAACTTAATCTTCAT[G/T]TCTAAAAACTTAATC | 22992 |
rs11227695 | snp | C/T | 0.0763149 | 0.179815 | intron-variant | KDM2A | GRCh38.p7 | 11:67125294 | CGAGTGATCTTCCCA[C/T]GTCAGCTTCCCAGGT | 22992 |
rs11227696 | snp | C/T | 0.0547245 | 0.156101 | intron-variant | KDM2A | GRCh38.p7 | 11:67126829 | TATAAGCTACACTTT[C/T]TGGAACTTGGAACCA | 22992 |
rs11227697 | snp | A/G/T | 0.0829739 | 0.187678 | intron-variant | KDM2A | GRCh38.p7 | 11:67127703 | TTTTTTAAATTAATT[A/G/T]ATTTATTTATTTATT | 22992 |
rs11227699 | snp | A/G | 0.380529 | 0.213219 | intron-variant | KDM2A | GRCh38.p7 | 11:67131021 | CATCCAACGTCTCTT[A/G]TGTACTTTATACAGA | 22992 |
rs11227700 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | KDM2A | GRCh38.p7 | 11:67131709 | GAGCCACGACTTTCC[A/G]CCTACTTTAACATTT | 22992 |
rs11227701 | snp | A/G/T | 0.0733688 | 0.176922 | intron-variant | KDM2A | GRCh38.p7 | 11:67133683 | GCTGGGATTACAGGC[A/G/T]TGAGCCACCGCACCC | 22992 |
rs11227703 | snp | G/T | 0.0726307 | 0.176182 | intron-variant | KDM2A | GRCh38.p7 | 11:67137823 | TTTTTTTGAGAAGGG[G/T]TCTCAGCTCTGTCGC | 22992 |
rs11227704 | snp | G/T | 0.175576 | 0.238665 | intron-variant | KDM2A | GRCh38.p7 | 11:67139276 | TTGAGACGGAGTCTC[G/T]CTTTGTCCCCCAGGC | 22992 |
rs11227705 | snp | C/G | 0.172351 | 0.237636 | intron-variant | KDM2A | GRCh38.p7 | 11:67139503 | gcccacctcggcccc[C/G]caaagtgctaggatt | 22992 |
rs11227706 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67141279 | GATGCATAGATTGTA[A/G]TGACCAAGTCAGAGT | 22992 |
rs11227707 | snp | A/T | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67141684 | aaaaaaaaaaaaaaa[A/T]atatatatatatata | 22992 |
rs11227708 | snp | A/G | 0.161267 | 0.233723 | intron-variant | KDM2A | GRCh38.p7 | 11:67144581 | AATATAAATTTTTTA[A/G]AGACAAGGTCTTGCT | 22992 |
rs11227711 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67147815 | tccaagtagctgcga[C/T]tacaggcgcctgcca | 22992 |
rs11227713 | snp | A/G | 0.0681886 | 0.171594 | intron-variant | KDM2A | GRCh38.p7 | 11:67148791 | GGGCTATAAGAGCAA[A/G]ATTCCGTCTCAAAAA | 22992 |
rs11227715 | snp | C/T | 0.0681886 | 0.171594 | intron-variant | KDM2A | GRCh38.p7 | 11:67151443 | TGGAGTGCAATGGTG[C/T]CATCTCTGCTCGCTG | 22992 |
rs11227717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67156844 | CAGTGAGCCGAGATC[A/G]CGCCACTGCACTTCA | 22992 |
rs11227718 | snp | G/T | 0.0726307 | 0.176182 | intron-variant | KDM2A | GRCh38.p7 | 11:67157250 | CCCGGGAGGCGGAGC[G/T]GGCAGTGAGCCAAAA | 22992 |
rs11227720 | snp | C/T | 0.0547245 | 0.156101 | intron-variant | KDM2A | GRCh38.p7 | 11:67160049 | CATGAAAGTATATGT[C/T]ACTGTGATGGCATAC | 22992 |
rs11227722 | snp | G/T | 0.0547245 | 0.156101 | intron-variant | KDM2A | GRCh38.p7 | 11:67160892 | GCAGGAGAATTGCTT[G/T]AGCCCAGGAGTTCAA | 22992 |
rs11227723 | snp | C/T | 0.0733688 | 0.176922 | intron-variant | KDM2A | GRCh38.p7 | 11:67168690 | ATAGACAGCAATGTC[C/T]GTCTATCCACATATG | 22992 |
rs11227724 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67170429 | ttttttttttttttt[C/T]tgagatggagtctcg | 22992 |
rs11227725 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67170433 | tttttttttttttga[A/G]atggagtctcgctct | 22992 |
rs11227726 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67170452 | gagtctcgctctgtc[C/G]cccaggctggagtgc | 22992 |
rs11227727 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67170531 | cattctcctgcctga[A/G]cctcccgagtagctg | 22992 |
rs11227728 | snp | A/G | 0.129664 | 0.219133 | intron-variant | KDM2A | GRCh38.p7 | 11:67179576 | TGAGCCACCGCACCC[A/G]GCCTGGAATGCTGTT | 22992 |
rs11227730 | snp | A/G | 0.0189257 | 0.0954184 | intron-variant | KDM2A | GRCh38.p7 | 11:67192835 | GACGGTATAAGCCTA[A/G]AAGTGGGCCAAAGAG | 22992 |
rs11227731 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67198590 | TGGCGGGCGCCTGTA[A/G]TCCCAGCTATTTGGG | 22992 |
rs11227732 | snp | C/T | 0.0726307 | 0.176182 | intron-variant | KDM2A | GRCh38.p7 | 11:67200250 | AGACGGAGTCTCTCT[C/T]TGTTGCCCAGGCTGG | 22992 |
rs11227733 | snp | C/G | 0.040671 | 0.13668 | intron-variant | KDM2A | GRCh38.p7 | 11:67207923 | gtagttccagctact[C/G]aagaggctgaggtgg | 22992 |
rs11227734 | snp | A/T | 0.173643 | 0.238054 | intron-variant | KDM2A | GRCh38.p7 | 11:67208221 | aaattttaaaatttt[A/T]aaatttattattatt | 22992 |
rs11227735 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67211611 | ACAGTGAGACCCTGT[C/T]TCAAAAAAAAAAAAA | 22992 |
rs11227736 | snp | A/C | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67212353 | AAGGGCAACTTTTAC[A/C]TGCCTGTTATAGGAG | 22992 |
rs11227738 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67216030 | GTATACTTAATATAC[C/T]CTGGAAATGAATCTG | 22992 |
rs11227739 | snp | C/T | 0.0759488 | 0.179461 | intron-variant | KDM2A | GRCh38.p7 | 11:67217923 | TTATTTAGCCATTTT[C/T]TTCCTTAATGAAAAA | 22992 |
rs11227740 | snp | A/C | 0.0722614 | 0.17581 | intron-variant | KDM2A | GRCh38.p7 | 11:67218173 | CTCTATAGATAGGAC[A/C]TGTTCTGCAGGTGAT | 22992 |
rs11227741 | snp | A/T | 0.172351 | 0.237636 | intron-variant | KDM2A | GRCh38.p7 | 11:67220540 | ggtttcaagagagaa[A/T]taagcccaaaataaa | 22992 |
rs11227742 | snp | A/G | 0.0726307 | 0.176182 | intron-variant | KDM2A | GRCh38.p7 | 11:67221271 | GTAGCTTAGCAGAAT[A/G]CTAAGCTAGTATGGA | 22992 |
rs11227743 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | KDM2A | GRCh38.p7 | 11:67227546 | AGCTTCTTGGTGGTT[C/T]TAAATGGTCTTCCTC | 22992 |
rs11227744 | snp | A/C | 0.236144 | 0.249616 | intron-variant | KDM2A | GRCh38.p7 | 11:67229752 | TTGCGCACCTGTAGT[A/C]CCAGGTACTCGGGAG | 22992 |
rs11227745 | snp | G/T | 0.0681886 | 0.171594 | intron-variant | KDM2A | GRCh38.p7 | 11:67233145 | CAATGGGTATGTATA[G/T]TAGAAAGCTAATCTA | 22992 |
rs11227746 | snp | G/T | 0.235854 | 0.249599 | intron-variant | KDM2A | GRCh38.p7 | 11:67234649 | AGACGCAGGCAGATC[G/T]CTTGAGACCAGCCTG | 22992 |
rs11227747 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | KDM2A | GRCh38.p7 | 11:67235677 | cctaggctggggtgc[A/G]gtggcgccatctcgg | 22992 |
rs11227749 | snp | C/T | 0.175254 | 0.238565 | intron-variant | KDM2A | GRCh38.p7 | 11:67237803 | aattaagaaattagc[C/T]gagcatggtattgtg | 22992 |
rs11227750 | snp | C/T | 0.0722614 | 0.17581 | intron-variant | KDM2A | GRCh38.p7 | 11:67247716 | AGGCGTGAGCCACCA[C/T]GCCCGGCCAACTTTA | 22992 |
rs11227751 | snp | A/G | 0.0722614 | 0.17581 | intron-variant | KDM2A | GRCh38.p7 | 11:67247721 | TGAGCCACCATGCCC[A/G]GCCAACTTTACAATC | 22992 |
rs11227752 | snp | A/T | 0.0681886 | 0.171594 | intron-variant | KDM2A | GRCh38.p7 | 11:67249312 | ATTACCTTCTAATAC[A/T]TTGGAAAAGGTAGCA | 22992 |
rs11227753 | snp | C/T | 0.0119198 | 0.0762746 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255019 | CAACAGCCTCTACTG[C/T]CTGTCTGACGAGAAG | 22992 |
rs11290221 | in-del | -/T | 0.186105 | 0.241697 | intron-variant | KDM2A | GRCh38.p7 | 11:67197176 | TTATCAGAAATAAAC[-/T]TTTTTTTTTTTTTTT | 22992 |
rs11297347 | in-del | -/T | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67182550 | TTTTTTTTTTTTTTT[-/T]GAGACGCAGTCTCCC | 22992 |
rs11335055 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67168973 | ATTTAATCCATGTAG[-/T]TTTTTTTTTTTTTTT | 22992 |
rs11373238 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67222060 | TAACTCTGTCATTCT[-/T]TTTTTTTTTTTTTTT | 22992 |
rs11416399 | in-del | -/A | 0.104149 | 0.203046 | intron-variant | KDM2A | GRCh38.p7 | 11:67197996 | ACAATAAAGTAAGAT[-/A]AAAAATTCCTTAAAT | 22992 |
rs11501507 | snp | C/T | 0.176219 | 0.238865 | intron-variant | KDM2A | GRCh38.p7 | 11:67189611 | TTGGCAGGCTGAGGC[C/T]GGTGGATCACCTGAG | 22992 |
rs11600579 | snp | A/C | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67170161 | GTACCGAGTTCAAAC[A/C]CCTTGTGATAGAAAA | 22992 |
rs11601878 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67249911 | CCAAGGCAGGTGGAT[C/T]ACTTGAGCCCAGGAG | 22992 |
rs11603271 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67216876 | ggtgagctgagatcg[C/T]gccattgcactctag | 22992 |
rs11604248 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | KDM2A | GRCh38.p7 | 11:67194057 | TTTAAAATTTAATCT[C/T]ATTTCTTTGAGTGTT | 22992 |
rs11606524 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67173037 | accctgtcacccagg[C/T]tggagtgcagtggtg | 22992 |
rs11819783 | snp | C/T | 0.168135 | 0.236216 | intron-variant | KDM2A | GRCh38.p7 | 11:67236216 | GCTCACTGCAGCCTC[C/T]GCCTGTCGGGTTCAA | 22992 |
rs11822036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67139445 | agatgggttttctcc[A/G]tgttggccaggctgg | 22992 |
rs11824081 | snp | C/T | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67187665 | ctgcaacctctgtct[C/T]ctggttcaagcgatt | 22992 |
rs11825309 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | KDM2A | GRCh38.p7 | 11:67137334 | atgtcagtggttgca[A/G]tgtagagaaagggtc | 22992 |
rs11826883 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | KDM2A | GRCh38.p7 | 11:67127195 | ctcaaccgcctggct[C/G]aagtggtcctcccat | 22992 |
rs12222166 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67201218 | aaTATATATATATAT[A/G]TGTGTGTGTGTGTGT | 22992 |
rs12223518 | snp | A/G | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67162081 | TTACTTTGCCTCTCA[A/G]GAATTTCCTTCCACT | 22992 |
rs12223898 | snp | C/T | 0.0663309 | 0.169604 | intron-variant | KDM2A | GRCh38.p7 | 11:67253029 | CTTAAGTGTCAGTCT[C/T]CCAGGCAGCACTCTG | 22992 |
rs12224613 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67154605 | cctggctaatttttt[C/T]ttttttttttttagg | 22992 |
rs12225293 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67201938 | ccagcctgggcatga[A/G]agtgagaccctgtct | 22992 |
rs12225294 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67201944 | tgggcatgagagtga[A/G]accctgtctctaaaa | 22992 |
rs12225313 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67202148 | attagaaatggagtc[A/G]aagatgcgactgaat | 22992 |
rs12225321 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67202199 | cttgagcagatggaa[A/G]agttgcttcttatgg | 22992 |
rs12271217 | snp | A/G | 0.117537 | 0.212022 | intron-variant | KDM2A | GRCh38.p7 | 11:67242276 | ACTCtgtgggtgtgt[A/G]tatgtgtgtgtgtgt | 22992 |
rs12271777 | snp | C/T | 0.236724 | 0.249647 | intron-variant | KDM2A | GRCh38.p7 | 11:67133259 | cgtgcgccaccacac[C/T]gcgctaattttgtgt | 22992 |
rs12274592 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67213573 | gaccagcctggccaa[A/G]atggtgaaaccctgt | 22992 |
rs12274743 | snp | G/T | 0.175576 | 0.238665 | intron-variant | KDM2A | GRCh38.p7 | 11:67234954 | gatcaagaccatcct[G/T]gctaacatggtgaaa | 22992 |
rs12274763 | snp | C/T | 0.161596 | 0.233848 | intron-variant | KDM2A | GRCh38.p7 | 11:67183898 | tggattgcttgagtc[C/T]aggagtttgagatca | 22992 |
rs12275826 | snp | A/G | 0.172351 | 0.237636 | intron-variant | KDM2A | GRCh38.p7 | 11:67166646 | aggaggatctcttga[A/G]gcaaggagttctggg | 22992 |
rs12276351 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67211271 | aagtgtgcatttcag[G/T]gagttttgacaaaca | 22992 |
rs12278847 | snp | A/C | 0.498964 | 0.02274 | intron-variant | KDM2A | GRCh38.p7 | 11:67233500 | CTACTAAAAATACAA[A/C]AATTAGCTGGGTGTG | 22992 |
rs12278848 | snp | A/G | 0.498964 | 0.02274 | intron-variant | KDM2A | GRCh38.p7 | 11:67233502 | ACTAAAAATACAAAA[A/G]TTAGCTGGGTGTGGT | 22992 |
rs12278855 | snp | A/G | 0.496905 | 0.0392151 | intron-variant | KDM2A | GRCh38.p7 | 11:67233545 | taatcccagctactc[A/G]ggaggctgaggcagg | 22992 |
rs12278858 | snp | A/G | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67233564 | ggctgaggcaggaga[A/G]tcccttgaacctggg | 22992 |
rs12279118 | snp | A/C/G | 0.130008 | 0.219321 | intron-variant | KDM2A | GRCh38.p7 | 11:67146167 | cagctaatttttttt[A/C/G]tatttttagtagaga | 22992 |
rs12282264 | snp | C/T | 0.236144 | 0.249616 | intron-variant | KDM2A | GRCh38.p7 | 11:67187905 | AATCAAAGAATGGTT[C/T]CAAGAGGggcctggt | 22992 |
rs12282634 | snp | A/G | 0.163236 | 0.234461 | intron-variant | KDM2A | GRCh38.p7 | 11:67188399 | aggcaggagaatggc[A/G]tgaacccgggaggta | 22992 |
rs12282851 | snp | C/T | 0.175576 | 0.238665 | intron-variant | KDM2A | GRCh38.p7 | 11:67138921 | ATTAACTAGAGGTAG[C/T]TACCTTAATTTCACA | 22992 |
rs12284313 | snp | A/G | 0.120326 | 0.21374 | intron-variant | KDM2A | GRCh38.p7 | 11:67242278 | TCTGTGGGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 22992 |
rs12284445 | snp | C/T | 0.161596 | 0.233848 | intron-variant | KDM2A | GRCh38.p7 | 11:67124472 | gcctgccaccatgcc[C/T]ggctaatttttttgt | 22992 |
rs12284546 | snp | C/T | 0.159622 | 0.233092 | upstream-variant-2KB, utr-variant-5-prime | KDM2A, LOC107984341 | GRCh38.p7 | 11:67118674 | CCCAGGCCTCCCGGC[C/T]CTCAGGTTGTGTGAC | 22992 |
rs12285582 | snp | C/T | 0.175897 | 0.238765 | intron-variant | KDM2A | GRCh38.p7 | 11:67246189 | AGAATGGGACACTTG[C/T]GATGGGAGTGCCAGC | 22992 |
rs12285720 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67165310 | tatttttagtagaga[A/C/T]gaggtttctccatgc | 22992 |
rs12286106 | snp | C/T | 0.172351 | 0.237636 | intron-variant | KDM2A | GRCh38.p7 | 11:67125150 | acaggcttgagccac[C/T]gcacccagccTGGAG | 22992 |
rs12286762 | snp | C/T | 0.172351 | 0.237636 | intron-variant | KDM2A | GRCh38.p7 | 11:67201008 | accatctggctaaca[C/T]ggtgaaacccagtct | 22992 |
rs12287003 | snp | C/G | 0.0262898 | 0.111596 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255598 | TGGTGCTGTTGAGAT[C/G]TCCCAAACCTCACGT | 22992 |
rs12287355 | snp | C/T | 0.175576 | 0.238665 | intron-variant | KDM2A | GRCh38.p7 | 11:67247128 | gagtcttgctccttt[C/T]gcctaggctagagtg | 22992 |
rs12288048 | snp | A/G | 0.299664 | 0.245017 | intron-variant | KDM2A | GRCh38.p7 | 11:67244294 | CAGCAGGGTAAATGC[A/G]AATGCTAAGAAATGT | 22992 |
rs12289064 | snp | A/G | 0.00916011 | 0.0670533 | intron-variant | KDM2A | GRCh38.p7 | 11:67166488 | acggtgcctggctGA[A/G]AAACTGAATATTTCT | 22992 |
rs12289324 | snp | G/T | 0.129664 | 0.219133 | intron-variant | KDM2A | GRCh38.p7 | 11:67218152 | TTAGCCCTAGTAATT[G/T]AGAATCTCTATAGAT | 22992 |
rs12290300 | snp | C/T | 0.161596 | 0.233848 | intron-variant | KDM2A | GRCh38.p7 | 11:67223531 | cctcagcctcctgag[C/T]agctgggaccacaga | 22992 |
rs12292083 | snp | C/G/T | 0.496905 | 0.0392151 | intron-variant | KDM2A | GRCh38.p7 | 11:67233544 | gtaatcccagctact[C/G/T]aggaggctgaggcag | 22992 |
rs12292088 | snp | C/G | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67233567 | tgaggcaggagaatc[C/G]cttgaacctgggagg | 22992 |
rs12292708 | snp | C/T | 0.172351 | 0.237636 | intron-variant | KDM2A | GRCh38.p7 | 11:67198634 | agaatggcgtgaacc[C/T]ggaaggcggaggttg | 22992 |
rs12293258 | snp | C/G | 0.175897 | 0.238765 | intron-variant | KDM2A | GRCh38.p7 | 11:67158757 | catgcccaaagtgct[C/G]gtattataggcgtga | 22992 |
rs12293524 | snp | A/G | 0.236144 | 0.249616 | intron-variant | KDM2A | GRCh38.p7 | 11:67216995 | cacgcctgtaatcca[A/G]cactttgggaggcca | 22992 |
rs12293866 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67201205 | tctcaaaaaaaaaaa[A/T]aTATATATATATATG | 22992 |
rs12293868 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67201207 | tcaaaaaaaaaaaTA[A/T]ATATATATATATGTG | 22992 |
rs12294589 | snp | A/G | 0.147991 | 0.228242 | intron-variant | KDM2A | GRCh38.p7 | 11:67192490 | tctcttggtgccctg[A/G]ctggagtgcagtggc | 22992 |
rs12294777 | snp | A/G | 0.161596 | 0.233848 | intron-variant | KDM2A | GRCh38.p7 | 11:67222901 | GAAAAATAAGGGGGA[A/G]AAAAAAAAAAggcca | 22992 |
rs12295689 | snp | G/T | 0.0437281 | 0.141251 | intron-variant | KDM2A | GRCh38.p7 | 11:67180932 | ctcccaaagtgctgg[G/T]attacaggtatgagc | 22992 |
rs12365685 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67179499 | gctggtctctaatct[C/G]gaactcccgacctca | 22992 |
rs12417887 | snp | C/G | 0.0810805 | 0.184299 | intron-variant | KDM2A | GRCh38.p7 | 11:67144360 | tgggttcaactgatt[C/G]tcctgcctcagcctc | 22992 |
rs12419315 | snp | G/T | 0.116838 | 0.211584 | intron-variant | KDM2A | GRCh38.p7 | 11:67143956 | ACTAttttttttttt[G/T]tgtgagacggagtct | 22992 |
rs12420356 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67247076 | atatatatatatTTT[A/T]ttttttttttttttt | 22992 |
rs12420479 | snp | C/T | 0.120674 | 0.21395 | intron-variant | KDM2A | GRCh38.p7 | 11:67126003 | gtaatcccagcactt[C/T]gggaggctgaggcgg | 22992 |
rs12420556 | snp | A/G | 0.122411 | 0.214991 | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67238829 | TCTAAAAAAGACCCA[A/G]ACTGTTTCTGCTAAG | 22992 |
rs12420594 | snp | C/G | 0.120674 | 0.21395 | intron-variant | KDM2A | GRCh38.p7 | 11:67171631 | GTTAGCTTGGGTCAG[C/G]TTTACCTTTCTGTTT | 22992 |
rs12420763 | snp | C/T | 0.0711817 | 0.174832 | intron-variant | KDM2A | GRCh38.p7 | 11:67217944 | TAATGAAAAAGAAAT[C/T]GATGGATTACCACCA | 22992 |
rs12421213 | snp | C/T | 0.121369 | 0.214369 | intron-variant | KDM2A | GRCh38.p7 | 11:67154440 | ttctttctttctttc[C/T]ttcttttttaagaca | 22992 |
rs12421536 | snp | A/G | 0.119978 | 0.213528 | intron-variant | KDM2A | GRCh38.p7 | 11:67191815 | gcctctattcaatgt[A/G]gcactggaagtccta | 22992 |
rs12785783 | snp | G/T | 0 | 0 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206092 | AGATATTAATGTTCA[G/T]AGAAATTATATAACT | 22992 |
rs12785905 | snp | C/G | 0.0271762 | 0.113356 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67184494 | ttagctgggcgtggt[C/G]gtgggcgcctgtaat | 22992 |
rs12785906 | snp | C/G | 0.0271762 | 0.113356 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67184495 | tagctgggcgtggtg[C/G]tgggcgcctgtaatc | 22992 |
rs12788405 | snp | C/T | 0.153332 | 0.230554 | intron-variant | KDM2A | GRCh38.p7 | 11:67232817 | GGTTCAAGCAGTTCT[C/T]GTGCCTCAGCCTCCT | 22992 |
rs12789637 | snp | A/C | 0.455621 | 0.142197 | intron-variant | KDM2A | GRCh38.p7 | 11:67233479 | CAAGATGGTAAAACC[A/C]CGTCTCTACTAAAAA | 22992 |
rs12790261 | snp | A/C | 0.0376037 | 0.131863 | intron-variant | KDM2A | GRCh38.p7 | 11:67220577 | tgtgtatcttatttt[A/C]tcatttttctctagg | 22992 |
rs12791976 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | KDM2A | GRCh38.p7 | 11:67236954 | GTGGGCTAAGAAATA[A/G]GAAATAAGTGCAGTC | 22992 |
rs12795237 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67216332 | GTGAAATCAGCAAAT[A/T]AAGATCTAAACCAAC | 22992 |
rs12798636 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67230552 | gattgcttgagccca[G/T]gaggttgaggctgca | 22992 |
rs12799792 | snp | A/C/G/T | 0.00239401 | 0.0345304 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67178177 | ttggaaggctgaggc[A/C/G/T]tgcagatcgcttgag | 22992 |
rs12799833 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67247071 | tatatatatatatat[A/T]tTTTTtttttttttt | 22992 |
rs12800059 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67142882 | acacccatataccca[A/T]tgccaagcttcaaca | 22992 |
rs12800892 | snp | A/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67178161 | ctgtaatcccagcag[A/T]ttggaaggctgaggc | 22992 |
rs12801044 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | KDM2A | GRCh38.p7 | 11:67138166 | ccgttaagtggcaca[A/G]gtctgTATTTGACCG | 22992 |
rs12805411 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67201774 | ctagactccatctca[A/G]aaaaaaaaaaaaaaa | 22992 |
rs12807675 | snp | A/G | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67147632 | AGAAGTGAGAATTTC[A/G]AGGATCAAGGGCTTT | 22992 |
rs12808051 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67147769 | tgcaactgccgcctc[A/C]tgggttcaagcgatt | 22992 |
rs17145414 | snp | A/G | 0.0726307 | 0.176182 | intron-variant | KDM2A | GRCh38.p7 | 11:67166082 | CAGAAATCAGGCAGT[A/G]AACAGAAGTATTCAG | 22992 |
rs17148080 | snp | G/T | 0.121369 | 0.214369 | intron-variant | KDM2A | GRCh38.p7 | 11:67169344 | GACATGAAAATCTAA[G/T]AGTGACAAGATTGGT | 22992 |
rs28589383 | snp | C/G | 0.309401 | 0.24284 | intron-variant | KDM2A | GRCh38.p7 | 11:67129830 | ACAGGAGAATCGCTT[C/G]AACTCGGGAGGCAGA | 22992 |
rs28604372 | snp | A/G | 0.237014 | 0.249662 | intron-variant | KDM2A | GRCh38.p7 | 11:67129772 | GAAAAATAGCCGGGC[A/G]TAGTGGCACATGCCT | 22992 |
rs34019423 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67216940 | AAGAAACAAACAACA[A/C]CAACAAAAAAACATG | 22992 |
rs34033663 | snp | C/T | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67195468 | ATTTTCTTTTTAAAC[C/T]CTTCTATTTTCCAAA | 22992 |
rs34036761 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67228682 | CAGAGTGAAACCCTG[-/T]TGCGAAAAAAAAAAA | 22992 |
rs34044085 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67211216 | AAAAACCAACTTTAT[G/T]GAGGTAAAATTGATG | 22992 |
rs34047718 | in-del | -/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67194174 | TTAGTTTAAAATGTT[-/C]CCATTTCTGTTCTCT | 22992 |
rs34111046 | snp | A/G | | | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67239062 | GTGAGAAGGCAGTGA[A/G]GTGTCTTGACAGGAT | 22992 |
rs34111100 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67230134 | GAGCTGAGATGGCAC[-/A]CACTGCACTCCAGCC | 22992 |
rs34189357 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67157746 | CAAGACTCCGTCTCC[-/A]AAAAAAAAAAAAAAA | 22992 |
rs34198150 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67230685 | ATCATACACATCTGT[G/T]AAAGCATGGAAAGAA | 22992 |
rs34245588 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67230666 | AAAAAAAACCCACAT[A/G]ATAATCATACACATC | 22992 |
rs34248598 | in-del | -/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67181076 | TTAAGCTCTAAATTT[-/C]CCTGTGGAAATTTAG | 22992 |
rs34263132 | in-del | -/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67160341 | CCGGTTTAGGAAGAG[-/C]ATTATAGCTTGAACC | 22992 |
rs34270166 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67184097 | GTGAGACCCTGTCTC[-/A]AAAAAAAAAAAAAAA | 22992 |
rs34301892 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67131384 | TGAGTACTTTCTCTC[-/T]TTTGAGGCTACTTTA | 22992 |
rs34306608 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67173637 | AAAGTCATCTGCCCG[C/G]CCTGGCCTCCCAGAG | 22992 |
rs34319163 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67169430 | TGTTGCCCAGGCTGA[A/T]ATGCAGTGGCACCAT | 22992 |
rs34319373 | in-del | -/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67183101 | CTCTGTTTTATTCAT[-/C]CCCCTTACTGTTTCT | 22992 |
rs34329359 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67233365 | CTCTACTAAAAATAC[-/A]AAAAAAGGCTCAGTG | 22992 |
rs34341669 | in-del | -/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67171226 | GGAAGATGTGGAAAG[-/C]CCTAAGAGAGCTACT | 22992 |
rs34369054 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67180951 | CAGGTATGAGCCACC[-/A]ACACCTGGCCCTTTT | 22992 |
rs34381674 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67224405 | TAATCCCAGGAGTTT[-/A]AGACCAGCCTGGACA | 22992 |
rs34402697 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67211275 | GTGCATTTCAGTGAG[-/T]TTTGACAAACATATT | 22992 |
rs34408848 | in-del | -/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67136230 | ATGGATTCTTTGACT[-/C]CCCATTTTAAAGTTT | 22992 |
rs34423150 | in-del | -/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67190291 | GTACATGCCTGTAAT[-/C]CCCAGCTACTCAGGA | 22992 |
rs34439497 | in-del | -/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67230960 | TTTTGGTTTTTTTTT[-/G]GTTTGTTTTTTTTTG | 22992 |
rs34463980 | in-del | -/A | 0.0158469 | 0.0875917 | intron-variant | KDM2A | GRCh38.p7 | 11:67249974 | GACCCCCTCTCCAAC[-/A]GTGACCTTTCTTCTC | 22992 |
rs34494813 | in-del | -/AA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67195394 | AAAAAAAAAAAAAAA[-/AA]GTTGAATAACATTAA | 22992 |
rs34512731 | in-del | -/A | 0.0162398 | 0.0886349 | intron-variant | KDM2A | GRCh38.p7 | 11:67220778 | TAGCATGAAATACTT[-/A]AAACAAATGAGTGTG | 22992 |
rs34517858 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67124615 | CTGTGCCTGGCCCAC[-/T]TTTTTTTTTTTTTTT | 22992 |
rs34535955 | in-del | -/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67228478 | GGCGAATGGCTTGAG[-/C]CCCAGGAGTTAAGAC | 22992 |
rs34544708 | in-del | -/AC | 0.418161 | 0.184991 | intron-variant | KDM2A | GRCh38.p7 | 11:67168546 | TGTATGAATTATAAT[-/AC]ACACACACACACACA | 22992 |
rs34568734 | in-del | -/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67181706 | GTAAATATATAATCA[-/C]CCTATATTTTTAAAA | 22992 |
rs34579576 | in-del | -/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67124609 | AGCCACTGTGCCTGG[-/C]CCCACTTTTTTTTTT | 22992 |
rs34605343 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67249316 | CTTCTAATACATTGG[-/A]AAAAGGTAGCACCCA | 22992 |
rs34625880 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67147596 | AGCCAGTGAACCTAG[G/T]TAAACCTTATTAAAG | 22992 |
rs34702668 | snp | C/G/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206760 | AAATAAACAAACTTA[C/G/T]GTCTCTTTGACTCCA | 22992 |
rs34749964 | snp | C/T | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67147563 | AAAAAAAAGATGCAA[C/T]TTTCACTGGATTTCA | 22992 |
rs34760535 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67253512 | CTGCCCTCAGCACCT[-/C]CCAGCTGCCCCCTTC | 22992 |
rs34761033 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67122282 | TGGTTCTCGAATACA[-/T]TTTTCTAGTGATCCT | 22992 |
rs34803380 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67157747 | CAAGACTCCGTCTCC[-/A]AAAAAAAAAAAAAAA | 22992 |
rs34808646 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67180908 | TGAGGTGATCTGCCC[-/A]ACCTTGGCCTCCCAA | 22992 |
rs34811347 | in-del | -/AT | | | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67238615 | TACTATAAAAATAAC[-/AT]ATGTAGCCCCTGGCA | 22992 |
rs34861641 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67230635 | TGTCTCAAAACAAAC[A/C]AACCACAACATAAAA | 22992 |
rs34861865 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67147443 | CTACTCAGGAGGTTA[-/T]AGGCAGGAGAATGGC | 22992 |
rs34895479 | in-del | -/A/AA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67230175 | GCGAGACTCCGTCTC[-/A/AA]AAAAAAAAAAAAAAA | 22992 |
rs34898241 | in-del | -/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67219686 | GCCTCCCAAGTAGCT[-/G]GGGACCGTGGGTGCA | 22992 |
rs34925153 | snp | A/G | 0.0222008 | 0.102993 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67253595 | GGACTTGCTTACTCC[A/G]CCGGCTGATAAACCA | 22992 |
rs34956697 | in-del | -/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67152674 | TGTAGCTTACATTTT[-/G]GTTTCTTTTGAGCTC | 22992 |
rs35062999 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67141686 | AAAAAAAAAAAAATA[-/T]ATATATATATATATA | 22992 |
rs35109777 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67219896 | CGTTTTAGGGACTCC[-/A]AATTCTGTGAGGTTT | 22992 |
rs35150844 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67201193 | GCAAGACTCTGTCTC[-/A]AAAAAAAAAAATATA | 22992 |
rs35153256 | in-del | -/A | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67129907 | CAGAGACTCTGTCTC[-/A]AAAAAAAAAATTAAA | 22992 |
rs35180780 | in-del | -/T | 0.49998 | 0.00319482 | intron-variant | KDM2A | GRCh38.p7 | 11:67224461 | AAATTAACCCCTTTC[-/T]TTTTTTTTTTTTTTT | 22992 |
rs35234338 | in-del | -/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67254058 | CACCCAGTGCTCACA[-/C]CCCTGAAGGCATGGC | 22992 |
rs35235938 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67152841 | ATCAGATTTTTTTTT[G/T]GCTAGCAAAACAAAA | 22992 |
rs35247976 | snp | C/T | 0.157642 | 0.232314 | intron-variant | KDM2A | GRCh38.p7 | 11:67228252 | CTGTCACTCAATATG[C/T]TCTTGGTTTTTTAAT | 22992 |
rs35249322 | in-del | -/G | | | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67239888 | GGAGGGAGACAGGGC[-/G]GGGGGCTGTGGCTGA | 22992 |
rs35272877 | in-del | -/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67134646 | GTAGCTGGGATTACA[-/G]GGTATGCGTCGCCAC | 22992 |
rs35308559 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67203402 | GTAGTCTGAAAATAC[-/A]AAATAGTCTAGTAAT | 22992 |
rs35333315 | in-del | -/TGTG | 0.343477 | 0.231866 | intron-variant | KDM2A | GRCh38.p7 | 11:67172617 | ATTAGCTCTTATAGT[-/TGTG]TGTGTGTGTGTGTGT | 22992 |
rs35372040 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67212782 | GAATGAATGCGTGGT[-/A]AAAAAAAAAAAAAAT | 22992 |
rs35377682 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67184098 | GTGAGACCCTGTCTC[-/A]AAAAAAAAAAAAAAA | 22992 |
rs35420048 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67147469 | TGGCATGAACCTGGG[-/T]AGGTGGAGCTTGCAG | 22992 |
rs35453006 | in-del | -/G | 0.453575 | 0.145111 | intron-variant | KDM2A | GRCh38.p7 | 11:67170384 | TATCCTACCAAGCAT[-/G]GGGTTTTTTTTTTTT | 22992 |
rs35461506 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67210570 | AAATATATTAACATT[-/A]AAAGGGCGGAGAAGA | 22992 |
rs35475927 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67169414 | ATGAAGTTTCGCTCC[-/T]TGTTGCCCAGGCTGA | 22992 |
rs35550425 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67200117 | GGAGATCTGCTCAGG[-/A]AAAAAGGTTCCTTTC | 22992 |
rs35594143 | in-del | -/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67180884 | CAGGCTGGTCTCGAA[-/C]CTCCTGACCTGAGGT | 22992 |
rs35601441 | in-del | -/T | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67152990 | TGTCTTTTTTTTTTT[-/T]GGAGACTGCGTTTCA | 22992 |
rs35626753 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67240898 | CCCCAGTAACTGAGT[-/A]CTTGTATGTGTGAAC | 22992 |
rs35638288 | in-del | -/GA | 0.454302 | 0.144085 | intron-variant | KDM2A | GRCh38.p7 | 11:67171489 | GGAAAGTTGAGATCT[-/GA]GAGGTTAAATGATTT | 22992 |
rs35684401 | in-del | -/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67224461 | AAAATTAACCCCTTT[-/C]TTTTTTTTTTTTTTT | 22992 |
rs35737338 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67180953 | GGTATGAGCCACCAC[-/A]ACCTGGCCCTTTTTT | 22992 |
rs35744181 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67235917 | CCACTGCGCCCGGCC[-/A]AAGATATCCTTAACA | 22992 |
rs35749477 | multinucleotide-polymorphism | CC/GG | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67184494 | TTAGCTGGGCGTGGT[CC/GG]TGGGCGCCTGTAATC | 22992 |
rs35782422 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67175742 | TATGGTAGACCTAAT[-/A]AAAAGGTTGAGGTTT | 22992 |
rs35814671 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67230640 | CAAAACAAACAAACC[A/C]CAACATAAAAAAAAA | 22992 |
rs35825424 | in-del | -/A | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185638 | GCGAAACTCTGTCGC[-/A]AAAAAAAAAAAAAAG | 22992 |
rs35837453 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67121454 | ATCTGTGATTAAAAC[-/T]TTTTCGGGTGACTTT | 22992 |
rs35844084 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67224402 | ACTTAATCCCAGGAG[-/T]TTAAGACCAGCCTGG | 22992 |
rs35854959 | in-del | -/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67158453 | ACATTTTATGGTAAG[-/C]AGTGTTTAGTTTTGT | 22992 |
rs35855186 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67230965 | GTTTTTTTTTGTTTG[-/T]TTTTTTTTTGAGACA | 22992 |
rs35881675 | in-del | -/TG | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67242279 | CTGTGGGTGTGTGTA[-/TG]TGTGTGTGTGTGTGT | 22992 |
rs35929127 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67175654 | AAAGATCAGGGGAAC[-/T]TTTTTGCCTATCATA | 22992 |
rs35933878 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67230642 | AAACAAACAAACCAC[A/C]ACATAAAAAAAAAAA | 22992 |
rs35990675 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67169356 | TAATAGTGACAAGAT[G/T]GGTTTCTTTCTTTCT | 22992 |
rs35992831 | snp | C/T | 0.152001 | 0.229992 | intron-variant | KDM2A | GRCh38.p7 | 11:67179420 | CTGGGATTACAGGCA[C/T]GTGCCACTACGCCCA | 22992 |
rs36012339 | in-del | -/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67235055 | AGGCTGAGGCAGGAG[-/C]AATGGCGTGAACCCG | 22992 |
rs36019351 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | KDM2A | GRCh38.p7 | 11:67138578 | CAGAGGTCAGGAGTT[C/T]GAGACCAGCCTGACC | 22992 |
rs36065276 | in-del | -/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67175087 | ATTTCCTTACTGTTA[-/G]AAGTGGCCTTACCTT | 22992 |
rs36085596 | snp | A/G | 0.153332 | 0.230554 | intron-variant | KDM2A | GRCh38.p7 | 11:67142102 | GGAGTGCAGTGGCAC[A/G]ATCTCCGCTCACTGC | 22992 |
rs36094369 | in-del | -/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67209576 | GCCTCTCAAATAGCT[-/G]GGGATTACAGGGACA | 22992 |
rs55646146 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67147374 | GGTGAAACCCCGTCT[C/T]TACTAAAAATAAAGA | 22992 |
rs55670148 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67209650 | GGTTTCACCATGTTG[A/G]CCAGGCTTGTCTCGA | 22992 |
rs55700100 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67134063 | GCTTTCTGAGGATTT[-/T]GAAGGCAAAGACAAA | 22992 |
rs55899911 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67209616 | ACCCGGCTAATTTTT[C/G]TATTTTTAGTAGAGA | 22992 |
rs55905838 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67209634 | TTTTTAGTAGAGATG[A/G]GGTTTCACCATGTTG | 22992 |
rs55948440 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67209638 | TAGTAGAGATGGGGT[C/T]TCACCATGTTGGCCA | 22992 |
rs55981805 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67224135 | CCTGGTGAAGGTTTT[-/T]GAAAAGGGACTCCTA | 22992 |
rs56012601 | in-del | -/TT | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67247445 | TTTTTTTTTTTTTTT[-/TT]AAGACATGGTCTCCC | 22992 |
rs56061830 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67209663 | TGGCCAGGCTTGTCT[C/T]GAACCCCTGACCTCA | 22992 |
rs56078015 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67209617 | CCCGGCTAATTTTTG[A/T]ATTTTTAGTAGAGAT | 22992 |
rs56088284 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | KDM2A | GRCh38.p7 | 11:67132148 | TTATACTACTACTAT[A/G]AGGCCTATTCTGTGG | 22992 |
rs56171506 | snp | A/G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67242086 | CTAAAAAATAAAAAT[A/G/T]AAAAAAAATATATTT | 22992 |
rs56173916 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | KDM2A | GRCh38.p7 | 11:67133661 | GCCCACCTCGGCCTC[C/T]CAAAGTGCTGGGATT | 22992 |
rs56199255 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67195394 | AAAAAAAAAAAAAAA[-/A]GTTGAATAACATTAA | 22992 |
rs56316741 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67209550 | CCAGGTTCAAGCAAT[C/T]CTCCCACCTCAGCCT | 22992 |
rs56758864 | in-del | -/TTGGGG | | | intron-variant | KDM2A | GRCh38.p7 | 11:67142597 | GGGTTGGGGTTGGGG[-/TTGGGG]GGGCGTCAAGGCAAG | 22992 |
rs56831094 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | KDM2A | GRCh38.p7 | 11:67208051 | TTTAAAATAAAATGC[A/G]TTGTTTTTATACTGG | 22992 |
rs56867687 | in-del | -/A | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67157764 | AAAAAAAAAAAAAAA[-/A]CTTGCATTAGTGTTG | 22992 |
rs56973148 | in-del | -/A | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67156739 | AAAAAAAAAAAAAAA[-/A]TTAGCTGGGCATGGT | 22992 |
rs56973649 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | KDM2A | GRCh38.p7 | 11:67139983 | TGTTGGAACTATAGG[C/T]GTGAGCCACCGCACC | 22992 |
rs57327069 | snp | A/C | 0.102014 | 0.201495 | intron-variant | KDM2A | GRCh38.p7 | 11:67128930 | AAGCCACTAGAGTGG[A/C]GGAGGGTCTGGATGC | 22992 |
rs57344301 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67198942 | CACCACCATGCCTGG[A/C]TAATTTTTGTATTTT | 22992 |
rs57554464 | in-del | -/AAAGAAA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67228701 | GAAAAAAAAAAAAAA[-/AAAGAAA]GAAAGAACGATGATC | 22992 |
rs57724865 | snp | A/G | 0.0663309 | 0.169604 | intron-variant | KDM2A | GRCh38.p7 | 11:67183768 | CAAATAATGGGATCC[A/G]TGCTGTGGTCACTGA | 22992 |
rs57740370 | in-del | -/GTTTT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67235638 | GTTTTGTTTTGTTTT[-/GTTTT]TGAGACAGAGTCTTG | 22992 |
rs57946225 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | KDM2A | GRCh38.p7 | 11:67127986 | AAGTGCTGGGATTAC[A/G]GTTGTGAGCCAGCAC | 22992 |
rs58100805 | snp | A/C | 0.0726307 | 0.176182 | intron-variant | KDM2A | GRCh38.p7 | 11:67230025 | ACTAAAAATACAAAA[A/C]ATTAGCTAGACGTGG | 22992 |
rs58248218 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67128145 | GTGGCTGGTACCACA[A/G]ATACATGCCACCACA | 22992 |
rs58397599 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67188455 | CCACTGCACTCCAGC[C/T]TGGGCGACAGAGCAA | 22992 |
rs58629654 | in-del | -/TTTTTTTT | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67214222 | TTTTTTTTTTTTTTT[-/TTTTTTTT]GAGACGGAGTCTTGC | 22992 |
rs58651351 | in-del | -/TGTG | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67172647 | GTGTGTGTGTGTGTG[-/TGTG]GATTCCTTATAGTTT | 22992 |
rs58663339 | snp | A/C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67141215 | CCATTTCTTCATATG[A/C/T]GAAACAATTTTTCCA | 22992 |
rs59057433 | snp | C/T | 0.0744748 | 0.178019 | intron-variant | KDM2A | GRCh38.p7 | 11:67188436 | GCACTGAGCTGAGAT[C/T]GCGCCACTGCACTCC | 22992 |
rs59095406 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67247072 | ATATATATATATATA[A/T]TTTTTTTTTTTTTTT | 22992 |
rs59101290 | in-del | -/ATAT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67247069 | TATATATATATATAT[-/ATAT]TTTTTTTTTTTTTTT | 22992 |
rs59357038 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67128385 | TATTTATTTTAAGCC[-/T]TTTTTTTTTCTAGTA | 22992 |
rs59421048 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | KDM2A | GRCh38.p7 | 11:67180480 | CGGCCTCTTCCTCCT[C/T]CTTCTATCCCTTGGT | 22992 |
rs59551907 | snp | A/G | 0.155656 | 0.231515 | intron-variant | KDM2A | GRCh38.p7 | 11:67187075 | TGAAGTCAAACTGGT[A/G]TTAATTAAAAATAGA | 22992 |
rs59766879 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67136798 | TTCAGATACCATGTA[G/T]GGCGCTCTGGCTTAC | 22992 |
rs59801773 | in-del | -/AA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67125962 | AAAAAAAAAAAAAAA[-/AA]GGCCAGGCACAGTGT | 22992 |
rs60035886 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67156738 | AAAAAAAAAAAAAAA[-/A]TTAGCTGGGCATGGT | 22992 |
rs60287734 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67142221 | TCTGCATTTTTAGTA[A/G]AGGTGGGGTTTGACC | 22992 |
rs60562395 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67132306 | TTTGTTTTTTGGATA[G/T]GGAGTCTCACTGCGA | 22992 |
rs60751057 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | KDM2A | GRCh38.p7 | 11:67186994 | TATAAGGATGTGGTT[C/T]TGTGACATCAGTAAC | 22992 |
rs60782221 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67142714 | CATCTCAAAAAAAAA[-/A]GTTAGAAATAAAAGT | 22992 |
rs60849469 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67202626 | AATACAAAAAAAAAA[-/A]CTAGCCAGGCATGGT | 22992 |
rs60924461 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67132308 | TGTTTTTTGGATATG[A/G]AGTCTCACTGCGATG | 22992 |
rs61044324 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | KDM2A | GRCh38.p7 | 11:67156415 | TGGTGAAACCCTGTC[C/T]CTACTAAAAATACAA | 22992 |
rs61320277 | in-del | -/GTGTGT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67201235 | TGTGTGTGTGTGTGT[-/GTGTGT]ATATATATATATTTC | 22992 |
rs61395951 | snp | A/G | 0.0726307 | 0.176182 | intron-variant | KDM2A | GRCh38.p7 | 11:67132574 | TTATAGGCATGAGCC[A/G]CTGCGTCCAGCCAGT | 22992 |
rs61525626 | snp | C/T | 0.122064 | 0.214785 | intron-variant | KDM2A | GRCh38.p7 | 11:67184046 | GAGACTGCAGTGATA[C/T]GTGATCACACCACTG | 22992 |
rs61663253 | snp | C/T | 0.0648419 | 0.167978 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67121114 | AAGGTCCCAAACTCA[C/T]GAAGAGGAACCTGAT | 22992 |
rs61889545 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67222602 | GGCACACCTCCCAGA[C/T]GGGGTGGTGGCCGGG | 22992 |
rs61889546 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67222913 | GGAAAAAAAAAAAAG[A/G]CCAGGCACAGTGGCT | 22992 |
rs61889547 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67224996 | ACAGGTATGCACCAC[C/T]ACGCTAATTTTTGTA | 22992 |
rs61889548 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67241757 | AGAAGATTTGGGTTT[C/T]AGGAGTTTCTGTCTA | 22992 |
rs61889549 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67243907 | GTTTAGATCCTGTAT[A/T]ATTTTTTTCCCCATA | 22992 |
rs61889550 | snp | A/G | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67245881 | GCTTCCAGGTGTTTA[A/G]TAGAGAATTATAGGA | 22992 |
rs61891315 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67127337 | TTTTTTTTGCTCAGT[A/C]TGGTCTTGAACTCCC | 22992 |
rs61891316 | snp | A/G | 0.0685596 | 0.171987 | intron-variant | KDM2A | GRCh38.p7 | 11:67128871 | TTGTTGAAAGCCTGG[A/G]TATATGCTCTTCTTT | 22992 |
rs61891317 | snp | C/T | 0.0726307 | 0.176182 | intron-variant | KDM2A | GRCh38.p7 | 11:67131867 | CTTGATCTGTTAAAA[C/T]GGCAGTATTGTGCAG | 22992 |
rs61891339 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67145879 | GTTACATCCTTTGGG[A/T]ATTTTTTTTTTTTTA | 22992 |
rs61891340 | snp | C/T | 0.0547245 | 0.156101 | intron-variant | KDM2A | GRCh38.p7 | 11:67146848 | GCCATGCTTTCCTCC[C/T]TCACTTTCGTGGATT | 22992 |
rs61891341 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67153871 | TCTTGCACTGATAAT[C/T]CCCTTTTTTTATTTT | 22992 |
rs61891342 | snp | C/T | 0.0726307 | 0.176182 | intron-variant | KDM2A | GRCh38.p7 | 11:67155907 | AGGTGTGAGCCACTG[C/T]GCCTGGCCGGTTTTT | 22992 |
rs61891343 | snp | C/T | 0.0551013 | 0.156571 | intron-variant | KDM2A | GRCh38.p7 | 11:67157372 | TTTTGAATAGTCTTT[C/T]GTGTGTGAGTGTGTG | 22992 |
rs61891344 | snp | C/T | 0.0681886 | 0.171594 | intron-variant | KDM2A | GRCh38.p7 | 11:67164711 | CGGCAACCTCCACCT[C/T]CCAGGGTCAAGCGAT | 22992 |
rs61891345 | snp | G/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67177686 | GACCTCCCTGAGGCT[G/T]TTTTACAGTTAATAT | 22992 |
rs61891346 | snp | C/T | 0.0729998 | 0.176553 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67179336 | TGGAATGCAATGGCA[C/T]GATCTTGGCTCACTG | 22992 |
rs61891347 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67180960 | AGCCACCACACCTGG[C/T]CCTTTTTTTTTTTTT | 22992 |
rs61891348 | snp | A/C | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67203002 | CCTGTCCGTCCGCCG[A/C]CAAAAAAAAAAAAAA | 22992 |
rs66466718 | snp | A/G | 0.153997 | 0.230832 | intron-variant | KDM2A | GRCh38.p7 | 11:67252170 | TAAGCCTGATAAAGA[A/G]CCTCTTTTGACCTGA | 22992 |
rs66535406 | in-del | -/T | 0.247337 | 0.249986 | intron-variant | KDM2A | GRCh38.p7 | 11:67182531 | AAAATTGAATAAGTC[-/T]TTTTTTTTTTTTTTT | 22992 |
rs66603590 | snp | A/G | 0.167158 | 0.235875 | intron-variant | KDM2A | GRCh38.p7 | 11:67167038 | AATTGAGATCATACC[A/G]TTGCACTCCAGCCTA | 22992 |
rs66968466 | in-del | -/C | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67168586 | CTTGTATGAATTATA[-/C]ATACACACACACACA | 22992 |
rs67686053 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67249975 | ACCCCCTCTCCAACG[-/A]TGACCTTTCTTCTCT | 22992 |
rs68165420 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67141686 | AAAAAAAAAAAAATA[A/T]ATATATATATATATA | 22992 |
rs71056179 | in-del | -/GTGTGT | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67168601 | TGTGTGTGTGTGTGT[-/GTGTGT]GTGTGTGTGTGTGTA | 22992 |
rs71056181 | in-del | -/GAGAGA | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67169748 | AAAAAAAAAGAGAGA[-/GAGAGA]GAGAGAGAGAGAGAA | 22992 |
rs71056183 | in-del | -/AAAAC | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67198797 | AGTGAGACTCCGTCA[-/AAAAC]AAAACAAAACAAAAC | 22992 |
rs71056184 | in-del | -/T | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67201805 | ACCAAGCATGGCTAA[-/T]TTTTTTTTTTTTTTT | 22992 |
rs71056185 | in-del | -/ATAG | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67203467 | TATTAATAATTATTA[-/ATAG]ATAATTAATAAATAT | 22992 |
rs71056186 | in-del | -/T | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67213773 | GAGAATACAGAAATC[-/T]TTTTTTTTTTTTTTT | 22992 |
rs71056187 | in-del | -/A | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67224462 | GCGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 22992 |
rs71457759 | snp | C/T | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67125721 | GAGGTGGAGGTTGCA[C/T]TAAGCAGAGATTGCG | 22992 |
rs71457760 | snp | G/T | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67159377 | CTCCTTTCTGGGTTG[G/T]CTGTTTTCTCATTGT | 22992 |
rs71457761 | snp | A/C | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67170287 | TGGAATATTAGATAA[A/C]CAATAATATAGCTAG | 22992 |
rs71457762 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | KDM2A | GRCh38.p7 | 11:67192830 | GTTTAGACGGTATAA[A/G]CCTAGAAGTGGGCCA | 22992 |
rs71457763 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67224322 | TAAAAGAAAGCTGTA[C/T]GGCCAGATATGGTGG | 22992 |
rs71457764 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | KDM2A | GRCh38.p7 | 11:67235856 | AACTCCTGACCTTGC[A/G]ATCCACCTGCCTTGG | 22992 |
rs71457765 | snp | A/G | 0.5 | 0 | missense, intron-variant | KDM2A | GRCh38.p7 | 11:67250641 | GAAGATGACAGTGCA[A/G]AGGAGGGGGGTGCAG | 22992 |
rs71457766 | snp | C/T | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255512 | GTGCGCGTCTCTCCT[C/T]CATCACACTCTCCCG | 22992 |
rs71461635 | in-del | -/T | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67130130 | AATTTTTTTTTTTTT[-/T]CTTGCACCAAAGCTT | 22992 |
rs71461636 | in-del | -/A | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67184115 | AAAAAAAAAAAAAAA[-/A]GGCAGGTGGGGCAGT | 22992 |
rs71461637 | in-del | -/T | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67200228 | GTGGTTTTTTTTTTT[-/T]CTTTTTAGACGGAGT | 22992 |
rs71462367 | snp | A/G | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67142317 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC | 22992 |
rs71462368 | snp | C/T | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67168592 | TTGTATGAATTATAA[C/T]ACACACACACACACA | 22992 |
rs71490510 | snp | A/T | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67211647 | AAAAAAAAAGAATAT[A/T]TATATAATAGCCTAT | 22992 |
rs72286994 | in-del | -/ATCT | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67203465 | TTATATTTATTAATT[-/ATCT]ATTAATAATTATTAA | 22992 |
rs72361897 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67156719 | GCGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 22992 |
rs72926998 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67141985 | ATTCCATCCATGTTC[C/T]GAAAATGACAGAATT | 22992 |
rs72927000 | snp | A/G | 0.0132527 | 0.0803163 | intron-variant | KDM2A | GRCh38.p7 | 11:67145549 | ATATGGTAGCACCCC[A/G]TTTTTTTTTTCATTA | 22992 |
rs72928907 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | KDM2A | GRCh38.p7 | 11:67155461 | CTGTAGGCAGGTACC[A/G]CCTTGGCTAAGTTTT | 22992 |
rs72928916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67166144 | GGCTAATGAAAATCA[A/G]GTTAAAAAATTGGTT | 22992 |
rs72928924 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67171475 | TGTTTACTTCCAAGG[A/G]AAAGTTGAGATCTGA | 22992 |
rs72928928 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67181264 | ATCCTTTTTATGGTC[C/T]TTTTATCGTTTTTAA | 22992 |
rs72928932 | snp | G/T | 0.0448719 | 0.142907 | intron-variant | KDM2A | GRCh38.p7 | 11:67183114 | CATCCCCTTACTGTT[G/T]CTGTTTTAAACCCTG | 22992 |
rs72928937 | snp | A/G | 0.030665 | 0.119967 | intron-variant | KDM2A | GRCh38.p7 | 11:67191472 | TGCATACTAAATTCA[A/G]CAGCATATTAAAAGG | 22992 |
rs72928961 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KDM2A | GRCh38.p7 | 11:67228717 | AAGAAAGAAAGAACG[A/G]TGATCAGTTGTCTAA | 22992 |
rs72928976 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67248793 | TCACATTTTTGTCAT[C/T]TTCACTTTTGTGGCC | 22992 |
rs72930739 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | KDM2A | GRCh38.p7 | 11:67251161 | GTTGGTTGAGAGCCT[A/G]TGATGTTCTAGTCAC | 22992 |
rs73493534 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67121078 | TTGAACATGACATGG[A/T]ACCACTTGCCCAAGA | 22992 |
rs73493536 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | KDM2A | GRCh38.p7 | 11:67128654 | TATATTTTGGGCCCC[C/T]AGAATGAGGATTAAA | 22992 |
rs73493541 | snp | G/T | 0.375 | 0.216506 | intron-variant | KDM2A | GRCh38.p7 | 11:67145988 | CCCGTTTTTTGTTTT[G/T]TTTTTTTTTGTTTTT | 22992 |
rs73501797 | snp | C/G | 0.0456336 | 0.143994 | intron-variant | KDM2A | GRCh38.p7 | 11:67204181 | TATAAAGTTTACCAT[C/G]ATAACCATTACGTTT | 22992 |
rs73501800 | snp | A/C | 0.0460142 | 0.144533 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67207331 | TATTATTAACATTAT[A/C]CATTGTCTTTCCCAT | 22992 |
rs73501802 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | KDM2A | GRCh38.p7 | 11:67222030 | ATGTATAATTCCATA[A/G]TAAAATACTCCTGTT | 22992 |
rs73503904 | snp | G/T | 0.031825 | 0.122064 | intron-variant | KDM2A | GRCh38.p7 | 11:67223255 | AGAAATTGATATGCG[G/T]CATAAGTAAAAAGCA | 22992 |
rs73503907 | snp | A/G | 0.0685596 | 0.171987 | intron-variant | KDM2A | GRCh38.p7 | 11:67225664 | AATCCCAGCTACTCG[A/G]GAGGCTGAGGCAGGA | 22992 |
rs73503911 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | KDM2A | GRCh38.p7 | 11:67241221 | TGAATTTTTCACCCT[A/G]GGGAGATTAGGAGCC | 22992 |
rs74189945 | multinucleotide-polymorphism | CCTCCC/TTGTCA | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67222554 | TCCACAAAGCCCCCA[CCTCCC/TTGTCA]TCCCGGACGGGGCGG | 22992 |
rs74219608 | multinucleotide-polymorphism | CAATGAGC/GGCCGGGT | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67222574 | CCGGACGGGGCGGCT[CAATGAGC/GGCCGGGT]GGGGGGCTGACACCC | 22992 |
rs74235910 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | KDM2A | GRCh38.p7 | 11:67205460 | GCCAGGGCAGGTGTT[C/T]GTTCGTCTTACAAGG | 22992 |
rs74332695 | snp | G/T | 0.0655868 | 0.168795 | intron-variant | KDM2A | GRCh38.p7 | 11:67143613 | TTTGTCTGTCTGTCT[G/T]TCTCTTTTTATTTAT | 22992 |
rs74334393 | snp | A/C | 0.00875587 | 0.0655841 | intron-variant | KDM2A | GRCh38.p7 | 11:67252560 | AGGCAAAAAATGATA[A/C]GGTGTGATCCCTGTA | 22992 |
rs74369977 | snp | A/C/G | 0.498832 | 0.0241331 | intron-variant | KDM2A | GRCh38.p7 | 11:67233522 | CTGGGTGTGGTGGCA[A/C/G]ACACCTGTAATCCCA | 22992 |
rs74370496 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | KDM2A | GRCh38.p7 | 11:67170931 | AACCAAAGTACCTGG[G/T]TTCTAGATCCTAGCC | 22992 |
rs74410043 | snp | C/T | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67233512 | CAAAAATTAGCTGGG[C/T]GTGGTGGCAGACACC | 22992 |
rs74485778 | snp | C/T | 0.0418186 | 0.138422 | upstream-variant-2KB, utr-variant-3-prime | KDM2A, LOC107984341 | GRCh38.p7 | 11:67117311 | CTTTCTATACTTCAG[C/T]TGTCTATCTTTAAAA | 22992 |
rs74511792 | snp | C/T | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67208566 | CCTGAGGTCAGGAGT[C/T]TGAGACCAGCTTGGC | 22992 |
rs74572611 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67179439 | CCACTACGCCCAGCT[A/T]ATTTTGTATTTTTAG | 22992 |
rs74581113 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67246169 | AATGGAGTGAGTGAC[A/G]CAACAGAATGGGACA | 22992 |
rs74586558 | snp | A/T | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67230648 | ACAAACCACAACATA[A/T]AAAAAAAAAACCCAC | 22992 |
rs74622597 | snp | A/C | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67188482 | GCAAGACTCTGTCTC[A/C]AAAAAAAAAAAAAAG | 22992 |
rs74654639 | snp | A/G | | | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67238036 | ATTCTTACTGAATAG[A/G]AAGTTTTAAGTAATG | 22992 |
rs74680971 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KDM2A | GRCh38.p7 | 11:67227562 | TAAATGGTCTTCCTC[A/G]AGTACCTTTTTTTGT | 22992 |
rs74775682 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67153328 | ACGTGTAATTGGAAA[A/G]GTGATGCTTTTCTGT | 22992 |
rs74779730 | snp | C/T | 0.118235 | 0.212457 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185631 | GTGACGAGCGAAACT[C/T]TGTCGCAAAAAAAAA | 22992 |
rs74846712 | snp | C/T | 0.119978 | 0.213528 | intron-variant | KDM2A | GRCh38.p7 | 11:67249521 | GGCTCCAGGAAAAGA[C/T]AAGTATCTAGAGAGC | 22992 |
rs74855080 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67174921 | CTGTGACACTGGGCC[C/T]AGTGAGGACTGGTAC | 22992 |
rs74869813 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | KDM2A | GRCh38.p7 | 11:67154826 | GTTCGAGGTTCATCT[G/T]TGTTTTGGCATGTAT | 22992 |
rs74922392 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | KDM2A | GRCh38.p7 | 11:67148019 | CTCTAGCTGATCATC[C/T]AGTGGTAATGTAAAT | 22992 |
rs74926133 | snp | G/T | 0.0372196 | 0.131242 | intron-variant | KDM2A | GRCh38.p7 | 11:67223892 | CAAATACCTATTGGT[G/T]GTTGTCTCTCTCCTC | 22992 |
rs74952667 | snp | C/G | 0.119978 | 0.213528 | intron-variant | KDM2A | GRCh38.p7 | 11:67229543 | ATTTTACTTTTACTG[C/G]ATAATTTTACTCATA | 22992 |
rs74963484 | snp | C/T | 0.172674 | 0.237741 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67179173 | TGAGCATTTTTCATG[C/T]GCTTATTGTACATTT | 22992 |
rs74987127 | snp | C/T | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67222607 | ACCTCCCAGACGGGG[C/T]GGTGGCCGGGCAGAG | 22992 |
rs75081047 | snp | C/G | 0.10237 | 0.201756 | upstream-variant-2KB, utr-variant-3-prime | KDM2A, LOC107984341 | GRCh38.p7 | 11:67117583 | GCAGGTTATATGATT[C/G]ACTCCATGCCCTACC | 22992 |
rs75085137 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | KDM2A | GRCh38.p7 | 11:67172685 | TGTACAAGATCATGT[A/G]ATTTGTGAATAGATG | 22992 |
rs75251389 | snp | C/T | 0.172351 | 0.237636 | intron-variant | KDM2A | GRCh38.p7 | 11:67194436 | CTGAATTACTAACAA[C/T]GTGTTCTTTTCTTAA | 22992 |
rs75375400 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67211800 | TTTGCATTTCTTAAT[C/G]CTAGAGTTACATAAT | 22992 |
rs75489850 | snp | G/T | 0.000863171 | 0.0207567 | intron-variant | KDM2A | GRCh38.p7 | 11:67246160 | GTCTCAGCTAATGGA[G/T]TGAGTGACACAACAG | 22992 |
rs75498182 | snp | C/T | 0.078151 | 0.181571 | intron-variant | KDM2A | GRCh38.p7 | 11:67146940 | ACATAGTTTACTGAT[C/T]TCATTTGAGATCATG | 22992 |
rs75520974 | snp | C/T | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67167609 | TTTTCCTTAAAGGTC[C/T]TACTGACTAAATATT | 22992 |
rs75665092 | snp | A/G | 0.0973687 | 0.197999 | intron-variant | KDM2A | GRCh38.p7 | 11:67242269 | ATAGCAGACTCTGTG[A/G]GTGTGTGTATGTGTG | 22992 |
rs75672654 | snp | C/G | 0.0799831 | 0.183287 | intron-variant | KDM2A | GRCh38.p7 | 11:67180553 | ATATATCTACCCCAC[C/G]AAAACTGAGGGTGGG | 22992 |
rs75744660 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67199980 | AAAAGCTTATTTACC[A/G]TTCCAAAATCCTAGG | 22992 |
rs75747404 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67125693 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCTGGGAG | 22992 |
rs75782795 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | KDM2A | GRCh38.p7 | 11:67226706 | CAGCCTGGGCAACAG[A/C]GCAAGACTCCGTCTC | 22992 |
rs75856624 | snp | A/T | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67145881 | TACATCCTTTGGGAA[A/T]TTTTTTTTTTTTAAT | 22992 |
rs75919687 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67180832 | TAATTTTTTTTTTTT[A/T]TATACTTTTAGTAGA | 22992 |
rs75987494 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | KDM2A | GRCh38.p7 | 11:67224439 | TAGTGAGACCCTGTC[C/G]GTACCAAAAATTAAC | 22992 |
rs76001637 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | KDM2A | GRCh38.p7 | 11:67132271 | CAAGTATGGACATAG[C/G]CATTAGAAGTTTTGT | 22992 |
rs76008703 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | KDM2A | GRCh38.p7 | 11:67168174 | TCTAGTAAGTGAAGA[A/G]AAACCCCCTAAAATT | 22992 |
rs76049209 | snp | A/C | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67126249 | AAAACTCCGTCTCAA[A/C]AAAAAAAAAAAAATG | 22992 |
rs76213096 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | KDM2A | GRCh38.p7 | 11:67236691 | AACCTATTTTCTCCT[C/T]TATAAAATATCTGTG | 22992 |
rs76237306 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67140201 | CGAAACCCTGTCTCT[A/G]CAAAAAATACAAAAA | 22992 |
rs76258697 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | KDM2A | GRCh38.p7 | 11:67123663 | GAAGAGCCTTTCCAG[C/G]AAGCAAAACTTTTAA | 22992 |
rs76284062 | snp | A/T | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67173892 | AACAATTTTTTTTTT[A/T]TATAAGATAGGGTCT | 22992 |
rs76289921 | snp | G/T | | | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67239048 | CAGTCCGAGTGGCTG[G/T]GAGAAGGCAGTGAGG | 22992 |
rs76317192 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67144747 | ATTTGGTATTTTTTT[G/T]GTAGTGATGGGTTTC | 22992 |
rs76499155 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185637 | AGCGAAACTCTGTCG[A/C]AAAAAAAAAAAAAAA | 22992 |
rs76500565 | snp | A/G | 0.102014 | 0.201495 | intron-variant | KDM2A | GRCh38.p7 | 11:67127018 | GTTTGTATACCTGAG[A/G]AGGTACTCAAGTGGG | 22992 |
rs76508699 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | KDM2A | GRCh38.p7 | 11:67195449 | TGGATTGCTGGTGAT[G/T]TTTATTTTCTTTTTA | 22992 |
rs76527041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67127961 | GCGATCTGCCTGCCT[C/T]GGCTTCCCAAAGTGC | 22992 |
rs76715188 | snp | A/T | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67156263 | CAAAAAAAAAAAAAA[A/T]TCACAAGGAGGATAA | 22992 |
rs76717961 | snp | A/T | 0.0372196 | 0.131242 | intron-variant | KDM2A | GRCh38.p7 | 11:67212660 | AAGAAAAGCACGAAC[A/T]TGTTACCACAAATTC | 22992 |
rs76723397 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant | KDM2A | GRCh38.p7 | 11:67196607 | AAGGACTTATGCTAA[A/G]TGAAATAACCCAGCC | 22992 |
rs76731458 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KDM2A | GRCh38.p7 | 11:67160944 | GAGCCTGTCTCTAAA[A/G]ATAAATAAATAATTA | 22992 |
rs76779146 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67209036 | CGCCTCCCGGGTTTA[C/T]GCCATTCTCCTGCCT | 22992 |
rs76806248 | snp | A/G | 0.498832 | 0.0241331 | intron-variant | KDM2A | GRCh38.p7 | 11:67233521 | GCTGGGTGTGGTGGC[A/G]GACACCTGTAATCCC | 22992 |
rs76863019 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | KDM2A | GRCh38.p7 | 11:67143657 | TATTTTTTTGAGATA[A/G]GGTCTCACTCCATCT | 22992 |
rs76865364 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185638 | GCGAAACTCTGTCGC[A/C]AAAAAAAAAAAAAAG | 22992 |
rs76887947 | snp | G/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67168260 | CTTGGTAGATGTCCA[G/T]TGAAGTTATGCTGAA | 22992 |
rs77060742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67161322 | TTGTATCCACGTGAA[A/G]CCTTTGAATTGTCTT | 22992 |
rs77062321 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | KDM2A | GRCh38.p7 | 11:67181560 | ATACACAAGTGTTTC[A/G]TATTAGAGGTAAATG | 22992 |
rs77100298 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67257278 | AACATGCATTTTTAC[C/T]GTGCACGTAAATTGG | 22992 |
rs77106193 | snp | A/G | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67222599 | TTGGGCACACCTCCC[A/G]GACGGGGTGGTGGCC | 22992 |
rs77112375 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | KDM2A | GRCh38.p7 | 11:67134818 | CCTTGAATTTTAGAT[A/C]AATCTAACACAAAAC | 22992 |
rs77198734 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67180027 | CTATGACCACTTGTA[C/G]GTAGGCATGAAAAAG | 22992 |
rs77199231 | snp | C/T | 0.0513262 | 0.151752 | intron-variant | KDM2A | GRCh38.p7 | 11:67153959 | GCATACATCATGACA[C/T]ATTATTCCTAAATGT | 22992 |
rs77207917 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | KDM2A | GRCh38.p7 | 11:67247998 | CTGTGTATTAGTTCC[C/T]GAGGGAAAGTGAAGG | 22992 |
rs77266676 | snp | G/T | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67182551 | TTTTTTTTTTTTTTT[G/T]AGACGCAGTCTCCCT | 22992 |
rs77319509 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | KDM2A | GRCh38.p7 | 11:67212530 | TTATGAATAGACTAG[A/G]TTCATGATATTGGAC | 22992 |
rs77360881 | snp | C/T | 0.0952156 | 0.196321 | intron-variant | KDM2A | GRCh38.p7 | 11:67174977 | AGGCTGCTAAAATCA[C/T]GTATATGAAAAGCAT | 22992 |
rs77420759 | snp | C/T | 0.172351 | 0.237636 | intron-variant | KDM2A | GRCh38.p7 | 11:67127672 | CCCCAAATTCAGCAG[C/T]GATTACCAGATTATC | 22992 |
rs77437160 | snp | A/G | 0.0644693 | 0.167566 | intron-variant | KDM2A | GRCh38.p7 | 11:67224237 | AATATGGGAGGAGAT[A/G]GGAACATTCTCAGGA | 22992 |
rs77467800 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | KDM2A | GRCh38.p7 | 11:67158460 | TATGGTAAGAGTGTT[C/T]AGTTTTGTAAGAAGC | 22992 |
rs77509449 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | KDM2A | GRCh38.p7 | 11:67173669 | GCTAAGATTACAGGT[A/G]TGAGCCACTGCACTT | 22992 |
rs77530290 | snp | C/T | 0.0689305 | 0.172377 | intron-variant | KDM2A | GRCh38.p7 | 11:67133582 | CAATTTTTATATTTT[C/T]AGTAGAGACGGGGTT | 22992 |
rs77531909 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | KDM2A | GRCh38.p7 | 11:67241042 | TTCTACTCTTGAACA[A/G]TCGCAGATCTTACTG | 22992 |
rs77551803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67149153 | CTGAATTTACTGAAT[A/G]TATTCCCTTCCTGAA | 22992 |
rs77556508 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | KDM2A | GRCh38.p7 | 11:67201498 | AGCCATGGCCCGGTG[C/T]GGTGGCTCACGCCTG | 22992 |
rs77557562 | snp | C/T | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67144267 | TTTTTTTTTTTTTTT[C/T]TCAAGACAGAGTCTC | 22992 |
rs77608813 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | KDM2A | GRCh38.p7 | 11:67197664 | CTGTCTTGTAAACTT[G/T]CTGTGATAGGATGTA | 22992 |
rs77616675 | snp | C/G | 0.079617 | 0.182947 | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67238441 | TCAATAGCTAGATCA[C/G]TGTTAAGGAAAGCCT | 22992 |
rs77661697 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KDM2A | GRCh38.p7 | 11:67161706 | TGGGGATATACACAA[A/G]GATTCTTTTATTAGG | 22992 |
rs77667801 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | KDM2A | GRCh38.p7 | 11:67146550 | GTCTCACTTTGTTAT[A/C]CACGCTGGAGTGCAG | 22992 |
rs77695318 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | KDM2A | GRCh38.p7 | 11:67160786 | CAAAAAAAACAACAA[A/C]AAAAAAATGAGATAG | 22992 |
rs77730138 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185448 | ACCAGCCTGCCCAAC[A/C]TGAAACCCTGTCTCT | 22992 |
rs77814456 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255575 | TCCCAGACCCGTGCC[A/G]ATCACACTGGTGCTG | 22992 |
rs77817849 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | KDM2A | GRCh38.p7 | 11:67161683 | AAAGTGGTTCTCAAC[A/G]TGTGGTCTGGGGATA | 22992 |
rs77831394 | snp | G/T | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67123302 | TTTTTTTTTTTTTTT[G/T]TGACTGCTAGAAAGG | 22992 |
rs77874215 | snp | A/G | 0.498832 | 0.0241331 | intron-variant | KDM2A | GRCh38.p7 | 11:67233519 | TAGCTGGGTGTGGTG[A/G]CAGACACCTGTAATC | 22992 |
rs77988791 | snp | A/G | 0.120674 | 0.21395 | intron-variant | KDM2A | GRCh38.p7 | 11:67128708 | GTTTTATTTTGCTGA[A/G]CATTAATCACTACTG | 22992 |
rs78028418 | snp | C/T | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67149722 | ACTAGGTATTAGAAT[C/T]TTTTTTTTTTTTTTT | 22992 |
rs78043817 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | KDM2A | GRCh38.p7 | 11:67146366 | TTTTACTTACTTTTT[A/G]TAGATCCTGAGGGCA | 22992 |
rs78126391 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | KDM2A | GRCh38.p7 | 11:67213952 | ACTGCAGCCTCAACC[C/T]CCTGGGTTTAAGCAA | 22992 |
rs78158435 | snp | G/T | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67197189 | ACTTTTTTTTTTTTT[G/T]TTGAGACAGGGTATT | 22992 |
rs78158850 | snp | G/T | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67146011 | TTGTTTTTTTTTTTT[G/T]AGACAGAGTCTATCT | 22992 |
rs78190743 | snp | A/G | 0.0644693 | 0.167566 | intron-variant | KDM2A | GRCh38.p7 | 11:67202330 | AAGTGAGTTTATAAA[A/G]CAGCAGTAGGGTTTG | 22992 |
rs78203875 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67248649 | AAAGAGAGGAACCAC[A/G]GCTGGGCTATTTGAG | 22992 |
rs78273812 | snp | C/T | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67180964 | ACCACACCTGGCCCT[C/T]TTTTTTTTTTTTTTA | 22992 |
rs78354165 | snp | A/C | 0.00291089 | 0.0380391 | intron-variant | KDM2A | GRCh38.p7 | 11:67181433 | CTGGATGTAGTTGCA[A/C]AATGGCCTCGTTACA | 22992 |
rs78359817 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KDM2A | GRCh38.p7 | 11:67137394 | ATTAATTAGGAGGCT[A/G]TTATATTGGTTCAGG | 22992 |
rs78382104 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67177666 | CTTTTGGATACCTCC[C/T]AAGAGACCTCCCTGA | 22992 |
rs78404433 | snp | A/G/T | 0.00835141 | 0.0640778 | intron-variant | KDM2A | GRCh38.p7 | 11:67168259 | ACTTGGTAGATGTCC[A/G/T]GTGAAGTTATGCTGA | 22992 |
rs78406849 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185639 | CGAAACTCTGTCGCA[A/C]AAAAAAAAAAAAAGT | 22992 |
rs78455991 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67145892 | GGAATTTTTTTTTTT[-/T]TAATTCCTGCTTTTC | 22992 |
rs78478405 | snp | C/T | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67162643 | ACTCCTGACCTCAAG[C/T]GATCCGCCCGCCTCG | 22992 |
rs78520278 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67179441 | ACTACGCCCAGCTTA[A/T]TTTGTATTTTTAGTA | 22992 |
rs78520298 | snp | A/C | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67181606 | ACCAAAAAAAAAAAA[A/C]CAACAAATTTAAATC | 22992 |
rs78551780 | snp | C/T | 0.0652144 | 0.168387 | intron-variant | KDM2A | GRCh38.p7 | 11:67129279 | GAACAAATAATAAAG[C/T]GTCTAGTTGATTTTA | 22992 |
rs78596078 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KDM2A | GRCh38.p7 | 11:67243385 | ACCAGTTACTCAGCT[A/G]TCTTCACAGATATGA | 22992 |
rs78680465 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | KDM2A | GRCh38.p7 | 11:67225376 | CGTGGTGGCTTATGC[C/T]TGTAATGCCAGCACT | 22992 |
rs78722728 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67131847 | TGAACTTTGAACTTA[C/T]TGCACTTGATCTGTT | 22992 |
rs78746957 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | KDM2A | GRCh38.p7 | 11:67154987 | ATCAGCATTTGTGTG[C/T]AAATATTTGAATACT | 22992 |
rs78756043 | snp | G/T | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67149738 | TTTTTTTTTTTTTTT[G/T]TGACAGTGTTTTCTC | 22992 |
rs78758407 | snp | C/T | 0.021333 | 0.101051 | intron-variant | KDM2A | GRCh38.p7 | 11:67154316 | GTAACAGAAAATTAA[C/T]CATTGATCATTTAGA | 22992 |
rs78776553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67135801 | GTGCTACATGTTGGG[C/T]AATCCCAAAAGTTGC | 22992 |
rs78853728 | in-del | -/G | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67170387 | CCTACCAAGCATGGG[-/G]TTTTTTTTTTTTCTT | 22992 |
rs78898449 | snp | A/C | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67126246 | AGCAAAACTCCGTCT[A/C]AAAAAAAAAAAAAAA | 22992 |
rs78909794 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | KDM2A | GRCh38.p7 | 11:67232371 | CTATGCTGGGTTAAC[A/G]TTGAGTAGCTTTAGC | 22992 |
rs79016315 | snp | A/G | 0.175576 | 0.238665 | intron-variant | KDM2A | GRCh38.p7 | 11:67249077 | GGGAAGGGGGCAGAA[A/G]GGAATTTTCTTACTT | 22992 |
rs79119009 | snp | A/T | 0.498832 | 0.0241331 | intron-variant | KDM2A | GRCh38.p7 | 11:67233525 | GGTGTGGTGGCAGAC[A/T]CCTGTAATCCCAGCT | 22992 |
rs79131669 | snp | A/C | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67208770 | TGAGACCCTGTCTCA[A/C]AAAAAAAAAAAAAAA | 22992 |
rs79159480 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | KDM2A | GRCh38.p7 | 11:67180638 | TATGTATTGTAGTGG[A/T]CAAAATTAATGTTTT | 22992 |
rs79204368 | snp | A/G/T | 0.498832 | 0.0241331 | intron-variant | KDM2A | GRCh38.p7 | 11:67233523 | TGGGTGTGGTGGCAG[A/G/T]CACCTGTAATCCCAG | 22992 |
rs79276870 | snp | A/C | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67157319 | AAGACTCCCGTCTCA[A/C]AAAAAAAAAAAACAA | 22992 |
rs79370337 | snp | A/C | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67157317 | GCAAGACTCCCGTCT[A/C]AAAAAAAAAAAAAAC | 22992 |
rs79426721 | snp | A/G | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67233513 | AAAAATTAGCTGGGT[A/G]TGGTGGCAGACACCT | 22992 |
rs79428209 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | KDM2A | GRCh38.p7 | 11:67235697 | CGCCATCTCGGCTCA[C/T]TGCAGCCTCCACCTC | 22992 |
rs79429303 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67132662 | GTTTCAGGTCGGGGT[A/G]GTCTAGAAAGAAATT | 22992 |
rs79501791 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | KDM2A | GRCh38.p7 | 11:67216271 | TTTCTGTACTTGGAA[A/G]TATAATAAATAGTGG | 22992 |
rs79621642 | snp | A/G | 0.00522111 | 0.0508261 | intron-variant | KDM2A | GRCh38.p7 | 11:67252600 | AAGAACGAGCCTCCA[A/G]GTACTCTGCTTTTCC | 22992 |
rs79628821 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67177983 | TATATGTGCAGTTCA[G/T]ATATATTGACTGAAA | 22992 |
rs79660270 | snp | A/T | 0.11963 | 0.213316 | intron-variant | KDM2A | GRCh38.p7 | 11:67146471 | TTCAGTTGAATATAA[A/T]TTTCTATCTACTGTG | 22992 |
rs79709263 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | KDM2A | GRCh38.p7 | 11:67240935 | CACCCCCCACACACA[C/T]ACCGACACAGTTTTC | 22992 |
rs79791276 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67123472 | AGTAGAATATTGTAT[C/T]GTTGGGATTTATTTT | 22992 |
rs79818775 | snp | A/G | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67222911 | GGGGAAAAAAAAAAA[A/G]GGCCAGGCACAGTGG | 22992 |
rs79860428 | snp | A/G | 0.0130921 | 0.0798413 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67256066 | TGAGCCCAGGCCTGT[A/G]TCTAGCCCCAGTGGC | 22992 |
rs79892773 | snp | A/T | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67247039 | GTTATAAATTATTTT[A/T]TATATATATATATAT | 22992 |
rs79913396 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67120914 | ATAAAAGTCCTGGGC[C/T]TTTTTTTTTTCTTGC | 22992 |
rs79953595 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | KDM2A | GRCh38.p7 | 11:67198306 | TTTTATTGCACTTTG[C/T]AGATAGTGTATTTTT | 22992 |
rs80026835 | snp | A/G | 0.498832 | 0.0241331 | intron-variant | KDM2A | GRCh38.p7 | 11:67233515 | AAATTAGCTGGGTGT[A/G]GTGGCAGACACCTGT | 22992 |
rs80029537 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67200725 | TTACCCAGGCTGGTT[G/T]AGAACTCCTGGGCTC | 22992 |
rs80153645 | snp | A/T | 0.0376037 | 0.131863 | intron-variant | KDM2A | GRCh38.p7 | 11:67242622 | ATTAGTACACAAGTA[A/T]GGGATTGGGAACAAA | 22992 |
rs80182307 | snp | G/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67257739 | TTTTTGTTGCTGATT[G/T]AGAGTCAATCTCCAA | 22992 |
rs80186481 | snp | A/G | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67162635 | GGTCTCGAACTCCTG[A/G]CCTCAAGTGATCCGC | 22992 |
rs80210155 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67168257 | GAACTTGGTAGATGT[A/C]CAGTGAAGTTATGCT | 22992 |
rs80241179 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | KDM2A | GRCh38.p7 | 11:67136093 | GTCACACTGCATATT[C/T]GAAAGTAGGAGATAA | 22992 |
rs80298919 | snp | G/T | 0.00835018 | 0.0640731 | intron-variant | KDM2A | GRCh38.p7 | 11:67196218 | GGTGCACGAGCAGGG[G/T]CTTGCAGCCCATGAG | 22992 |
rs80308020 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | KDM2A | GRCh38.p7 | 11:67128909 | ATTTTCTTGAATGCT[A/G]GGATTAAGCCACTAG | 22992 |
rs111272001 | snp | A/T | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67187679 | TCCTGGTTCAAGCGA[A/T]TCTCCTGCCTCAGCC | 22992 |
rs111273624 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KDM2A | GRCh38.p7 | 11:67172255 | AGGATTGTTTTGACT[A/G]TTCTGGTTTGCTGGT | 22992 |
rs111363689 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67130850 | AAGGTAGATGGTATC[A/G]TTTTAAACCTTGATT | 22992 |
rs111373093 | snp | A/G | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67187755 | AATTTTGTATTTTTA[A/G]TAGAGACGGGGTTTT | 22992 |
rs111379155 | snp | A/C | | | intron-variant | KDM2A | GRCh38.p7 | 11:67133637 | TGAACTCCTGACCTC[A/C]GGTGATCTGCCCACC | 22992 |
rs111438308 | snp | C/T | 0.444444 | 0.157135 | intron-variant | KDM2A | GRCh38.p7 | 11:67148312 | TGTAGTCTTAGCTGC[C/T]TGGGAGGTCGAGGCC | 22992 |
rs111449172 | snp | C/G/T | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67201724 | AGTGAGCCAAGATCA[C/G/T]ACCACCCCACCACAC | 22992 |
rs111450979 | snp | C/G | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67155226 | TTGCTATGTTGGCCA[C/G]GCTGGTCTCGAACTC | 22992 |
rs111502347 | snp | A/G | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67236020 | TACCATCCCATTAAT[A/G]TAAGAAAAAGTGTAT | 22992 |
rs111554623 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67224665 | TAGAGATGGGGTTTC[A/G]CTGTGTTAGCCAGGA | 22992 |
rs111585071 | snp | A/G | 0.172351 | 0.237636 | intron-variant | KDM2A | GRCh38.p7 | 11:67230537 | AGGCTATTGTGGGAG[A/G]ATTGCTTGAGCCCAG | 22992 |
rs111586786 | snp | C/G | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | KDM2A | GRCh38.p7 | 11:67239203 | CTTACAGGCAGAGGA[C/G]ACTGCTGGAATTGGG | 22992 |
rs111672685 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | KDM2A | GRCh38.p7 | 11:67240649 | TGTGGGCTTGTGTTT[A/C]AATGTTCTCCCGAAT | 22992 |
rs111685640 | snp | C/G/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255569 | CAGGAGTCCCAGACC[C/G/T]GTGCCGATCACACTG | 22992 |
rs111732073 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67219827 | AAGTGCTGGGATTAC[A/G]GGTGTGAGCCACTGC | 22992 |
rs111792524 | snp | A/G | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67211245 | TGTTCAGTAAAGTGG[A/G]CCCCCATTTTAAGTG | 22992 |
rs111889162 | snp | A/C | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67174715 | TTTTTAAGACATTTA[A/C]AATTCTTCATATTAT | 22992 |
rs111892128 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67149325 | GTACTGATACCTTTT[A/C]GGGTTGGTTGAGGAT | 22992 |
rs111898492 | snp | C/T | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67242277 | CTCTGTGGGTGTGTG[C/T]ATGTGTGTGTGTGTG | 22992 |
rs111921772 | snp | C/G | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67139273 | CTTTTGAGACGGAGT[C/G]TCGCTTTGTCCCCCA | 22992 |
rs111948829 | snp | G/T | 0.0236746 | 0.106192 | intron-variant | KDM2A | GRCh38.p7 | 11:67204586 | AAGCTCCGCCTCCTG[G/T]GTTCATGCCATTCTC | 22992 |
rs111981707 | in-del | -/T | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67219560 | AAATTTTAAATTTAA[-/T]TTTTTTTTTTTTAAG | 22992 |
rs111992957 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67162580 | CCAGCTAACTTTTGT[A/G]TTTTTAGTAGAGATG | 22992 |
rs111994192 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67229116 | GTTGTATTCTAGGCA[C/T]TATACTAAGCAATTT | 22992 |
rs112132478 | in-del | -/A | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67256352 | AGCTTTTTGCACTTT[-/A]AAAAAAAAAAGAAAG | 22992 |
rs112220079 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | KDM2A | GRCh38.p7 | 11:67150506 | ATTAGTACACATTGG[A/G]AAGTGGATTCCAGGC | 22992 |
rs112230357 | snp | A/G | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67233826 | AGAGACATCTAAAGA[A/G]GAGGCTTAGCATTAT | 22992 |
rs112231017 | snp | A/G | 0.00835141 | 0.0640778 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67256907 | GGTCTCCAGGCCCCA[A/G]TAATCTGGGGTTGAA | 22992 |
rs112254062 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | KDM2A | GRCh38.p7 | 11:67187668 | CAACCTCTGTCTCCT[G/T]GTTCAAGCGATTCTC | 22992 |
rs112255648 | snp | A/C | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67230931 | GACCAAAACTTCAGA[A/C]AAAAAAAAAAAGTTT | 22992 |
rs112269237 | snp | A/G | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67133392 | TAGGTGTGAGCCACC[A/G]TGCCTGGCCTATTTT | 22992 |
rs112282938 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67204020 | TGGCCAGGCTGGTCT[C/G]AAACTCCTGACCTCA | 22992 |
rs112302981 | snp | A/G | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67233279 | ATCCTAGCACTTTGA[A/G]AGGCCAAGGTGGGAG | 22992 |
rs112306431 | snp | A/G | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67253833 | TTGTGAGTTGGTGGA[A/G]TTTGGGGCCCAGAGA | 22992 |
rs112366319 | in-del | -/T | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67169298 | AAACAATGCCCTAAA[-/T]TTTTTTTTTTTAAAT | 22992 |
rs112393863 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | KDM2A | GRCh38.p7 | 11:67241148 | GAGTCCTACTCTTCG[A/T]CAGTGCGAAGTGGGG | 22992 |
rs112399635 | snp | C/G | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67170067 | GGCCCACAGTTTCAT[C/G]TTTTTAGAGGTCTAT | 22992 |
rs112402981 | snp | C/T | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67223553 | GACCACAGACGCACA[C/T]CACCACACCTGGCTA | 22992 |
rs112406399 | in-del | -/T | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67218540 | TAAAACATTATGAGA[-/T]TTTTTTTTTTGCAAT | 22992 |
rs112427094 | snp | C/G | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67204272 | TCAAGTTTTTTCACA[C/G]TGTGCAACCATCACC | 22992 |
rs112482435 | snp | C/T | 0.444444 | 0.157135 | intron-variant | KDM2A | GRCh38.p7 | 11:67155722 | CCCGGGTTCAAGCAA[C/T]TCTCCTGCCTCAGCC | 22992 |
rs112583326 | snp | C/T | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67123213 | ACTCCTGGCCTCAAG[C/T]GATCCTCCCACCTTG | 22992 |
rs112595059 | snp | C/T | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67170400 | GGGTTTTTTTTTTTT[C/T]TTTCTTTCTTTTTTT | 22992 |
rs112677118 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67232700 | TTTTTTTTTTTTTTA[A/T]TTTTAATTAATTAAT | 22992 |
rs112682042 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67129356 | CACTTTGGGAGACCA[A/G]GGCCAGTGGAATGCT | 22992 |
rs112684494 | in-del | -/A | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67126247 | GCAAAACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 22992 |
rs112827994 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | KDM2A | GRCh38.p7 | 11:67167606 | TTTTTTTCCTTAAAG[A/G]TCCTACTGACTAAAT | 22992 |
rs112889725 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67232917 | GTTTCACCATGTTGG[C/T]CAGGCTGGTCTCGAA | 22992 |
rs112900629 | snp | C/T | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67172768 | GCTAGAAATTTCTTG[C/T]CTAACTGCCCTAGCT | 22992 |
rs112912149 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67166187 | AAACAATATTTCTCT[C/G/T]TTTTTTTTTTTTTTT | 22992 |
rs112917552 | snp | A/G | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67222648 | CTTCCCAGTAGGGGC[A/G]GCCGGGCAGAGGCGC | 22992 |
rs112929673 | snp | C/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67192697 | TGATCCATCCGCCTT[C/G]GCCTCCCAAAGTGCT | 22992 |
rs112931679 | snp | A/G | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67228756 | TTGTTTTTGTTTTAG[A/G]GACAGGGCCTTGCCC | 22992 |
rs112953125 | snp | A/G | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67222649 | TTCCCAGTAGGGGCG[A/G]CCGGGCAGAGGCGCC | 22992 |
rs113021025 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67178720 | ATGGCACATAGCGTT[A/G]TTTCATTCCTTTTTG | 22992 |
rs113034815 | snp | C/G | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67134190 | AGGCTTTAGACAGTT[C/G]GAGATACTAGAAGAT | 22992 |
rs113044500 | snp | C/G | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67179490 | GTTGGTCAGGCTGGT[C/G]TCTAATCTCGAACTC | 22992 |
rs113067939 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67216834 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCCACAAG | 22992 |
rs113116797 | snp | A/G | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67210940 | TGAGCCCAAGAGTTC[A/G]AGACCACTCGGGAGG | 22992 |
rs113121267 | snp | A/C | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67224308 | AAATATGGCCTCTCT[A/C]AAAGAAAGCTGTATG | 22992 |
rs113122428 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | KDM2A | GRCh38.p7 | 11:67251366 | GCAGAGTCCAGTTTT[A/G]AAGCTTCCTTAATGA | 22992 |
rs113216545 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | KDM2A | GRCh38.p7 | 11:67253779 | GAATAGGGTAACTAT[A/G]AGCAGATAACTACCT | 22992 |
rs113318225 | snp | C/T | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67170408 | TTTTTTTCTTTCTTT[C/T]TTTTTTTTTTTTTTT | 22992 |
rs113336463 | snp | G/T | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67247596 | CCATGCCCAGCTAGT[G/T]TTGTGTTAAGTAGAG | 22992 |
rs113350825 | snp | G/T | 0.079617 | 0.182947 | intron-variant | KDM2A | GRCh38.p7 | 11:67222374 | AGCACATGTTTCAGA[G/T]AGCACAGGGTTGGGG | 22992 |
rs113372877 | snp | A/C | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67211801 | TTGCATTTCTTAATC[A/C]TAGAGTTACATAATC | 22992 |
rs113425273 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | KDM2A | GRCh38.p7 | 11:67187336 | AGTGGATTAAATTCC[C/G]CAATCAAAAGACAAG | 22992 |
rs113427726 | in-del | -/GT | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67170195 | TGATTAGAAATAGCA[-/GT]GTTTTCATTTCAGCC | 22992 |
rs113451915 | snp | C/T | 0.0017044 | 0.0291427 | synonymous-codon, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67254926 | ACGGCGCATTGCCAA[C/T]GTCACCTTGATCGAC | 22992 |
rs113462827 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67201798 | AAAAAAAAAAAAAAA[A/G]AAAAAAATTAGCCAT | 22992 |
rs113573619 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67161453 | AGTATGTTGTAGTAC[A/C]GTGTTTTGCACAGTT | 22992 |
rs113637609 | snp | C/T | | | intron-variant, utr-variant-5-prime | KDM2A | GRCh38.p7 | 11:67179395 | TCTCCTGCGTCAGCC[C/T]CCTGAGTAGCTGGGA | 22992 |
rs113642468 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | KDM2A | GRCh38.p7 | 11:67172523 | TTCCTTAGTTTTTTT[A/T]ATGCTATTATAAATG | 22992 |
rs113643152 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, missense | KDM2A, LOC107984341 | GRCh38.p7 | 11:67118426 | GAGGAGCCCCCGGGC[C/T]CAGGGCAGACGGGCC | 22992 |
rs113675375 | snp | A/G | 0 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67156580 | GAAAATTAGCCGGGC[A/G]TGGTGGTAGGCGCCT | 22992 |
rs113697506 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KDM2A | GRCh38.p7 | 11:67232400 | GCCTCTTTAGATTCA[A/G]ATTTATCTAGCATCA | 22992 |
rs113750876 | snp | A/G | 0.302686 | 0.244385 | intron-variant | KDM2A | GRCh38.p7 | 11:67201236 | TGTGTGTGTGTGTGT[A/G]TATATATATATTTCA | 22992 |
rs113751673 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67154878 | GGCTGAATAATATTC[C/T]GTTGTATGGATATAC | 22992 |
rs113769512 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67202777 | CGAGACTTCGTCTCA[A/G]AAAAAAAAAAGAAAA | 22992 |
rs113780245 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | KDM2A | GRCh38.p7 | 11:67215675 | TAGTCAATACGGTAG[A/G]AAAAAAAAAAACCTT | 22992 |
rs113853399 | snp | G/T | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67156111 | AAAATAGCTGTGCGT[G/T]GTGGCACATGCCTGT | 22992 |
rs113880816 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | KDM2A | GRCh38.p7 | 11:67130449 | CATGCCCGGCCTTAA[A/G]CTCTCCTGTTCTAAT | 22992 |
rs113933253 | snp | A/G | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67173493 | CAGCTCCTGACCTCA[A/G]TGATCAGCCTGTTTT | 22992 |
rs113978112 | snp | C/T | 0.5 | 0 | intron-variant | KDM2A | GRCh38.p7 | 11:67232567 | GACATACATGTGCCA[C/T]GTCAGTTTGCTGCAC | 22992 |
rs114020427 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185636 | GAGCGAAACTCTGTC[A/G]CAAAAAAAAAAAAAA | 22992 |
rs114051741 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | KDM2A | GRCh38.p7 | 11:67245028 | ATAATACATACACAA[A/G]ATGAGTTGTGTGTCA | 22992 |
rs114066138 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | KDM2A | GRCh38.p7 | 11:67254592 | AACTGATGGGGGACT[G/T]AGGCCTTGAGTAGTT | 22992 |
rs114336034 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67158752 | CCTTACATGCCCAAA[A/G]TGCTCGTATTATAGG | 22992 |
rs114355793 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | KDM2A | GRCh38.p7 | 11:67189375 | ACCAAAACTTATAGG[A/G]ATCAGTGAAAGCAAC | 22992 |
rs114381026 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67120731 | ACGGCCTTACAGGAG[G/T]GGTATGGGAAATTGT | 22992 |
rs114402602 | snp | G/T | 0.00218051 | 0.032947 | intron-variant | KDM2A | GRCh38.p7 | 11:67253439 | TATTACATGTCTCAT[G/T]CCATCCATTGCAGGA | 22992 |
rs114681982 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | KDM2A | GRCh38.p7 | 11:67169260 | CACCCGGCCTAATCC[A/G]TGTAGCTTTATATAA | 22992 |
rs114755064 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KDM2A | GRCh38.p7 | 11:67233919 | TCACTGGCTAAGATA[C/T]AGTGGCAGAGGCCAG | 22992 |
rs114903352 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | KDM2A | GRCh38.p7 | 11:67152173 | TACCAAAAAGCCAGG[C/T]GTGGTGGTGTGCACC | 22992 |
rs114916006 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67136273 | CAAAGTGCAGTTAAG[C/T]GTCTCAGATTATCCA | 22992 |
rs114920302 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67153645 | GCAACATAGTAAGAC[C/T]CAATGTCTACAAAAA | 22992 |
rs114925794 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67170354 | TACCCCAGGGAAGAT[C/T]CTTTGCTAATCCTTT | 22992 |
rs115172045 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | KDM2A | GRCh38.p7 | 11:67248797 | ATTTTTGTCATCTTC[A/G]CTTTTGTGGCCTGGC | 22992 |
rs115203158 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67157008 | ATTTACCCTCTGGCC[C/T]CTTTCATTAAAAGCT | 22992 |
rs115389405 | snp | C/G | 0.0372196 | 0.131242 | intron-variant | KDM2A | GRCh38.p7 | 11:67126415 | CGTTTCTCACACACA[C/G]ATTGTTTTTTGGCCG | 22992 |
rs115392803 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67227192 | TGGTTTGTGGACATA[A/C]CATTTTGGCAGACTA | 22992 |
rs115440009 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | KDM2A | GRCh38.p7 | 11:67212740 | ATGACTGACTTTCTT[A/G]CTGCAATTAAGAAAT | 22992 |
rs115478046 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | KDM2A | GRCh38.p7 | 11:67151043 | TGCTTGGAGGATATC[A/G]TGGTGGATAGTAGAA | 22992 |
rs115640717 | snp | G/T | 0.0799831 | 0.183287 | intron-variant | KDM2A | GRCh38.p7 | 11:67230365 | AGGCATGGTGGCTCA[G/T]GCCTGTGATCTCAGT | 22992 |
rs115657829 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | KDM2A | GRCh38.p7 | 11:67219488 | TCACTGATGGTTTAT[C/T]AAAACTTCCATTTTT | 22992 |
rs115691776 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67228526 | CAAAACCCCATCTCT[A/G]CAGAAACTACAGAAA | 22992 |
rs115692739 | snp | G/T | 0.0360663 | 0.129354 | intron-variant | KDM2A | GRCh38.p7 | 11:67203925 | CTTGCCTCAGCCTCC[G/T]AAGTAGCTGGGACTA | 22992 |
rs115736197 | snp | A/T | 0.248188 | 0.249993 | intron-variant | KDM2A | GRCh38.p7 | 11:67127707 | TTAAATTAATTAATT[A/T]ATTTATTTATTTATT | 22992 |
rs115813457 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | KDM2A | GRCh38.p7 | 11:67142558 | GGTGAAGTTGGCCGG[A/G]GGGTTGGGGTTGGGG | 22992 |
rs115872216 | snp | A/C | 0.117886 | 0.21224 | intron-variant | KDM2A | GRCh38.p7 | 11:67194695 | GTAGGTGGTATTAAA[A/C]CACAAGCTAGACCAT | 22992 |
rs115989931 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67147657 | GGCTTTCTCTGGAGA[C/T]TGAGTAGTTCCCTTT | 22992 |
rs116212640 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | KDM2A | GRCh38.p7 | 11:67143170 | GGGATGACAGGCATA[C/G]ACCAGTACACTCGGC | 22992 |
rs116224216 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | KDM2A | GRCh38.p7 | 11:67122070 | TTTGTTTTTCTTAGC[C/T]AAAGAGAGCTTTATT | 22992 |
rs116225543 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | KDM2A | GRCh38.p7 | 11:67224628 | ACCCGCCACCAAGCC[C/T]GGCCAATTTTTATAT | 22992 |
rs116240085 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67182140 | TTCTCTCCTTGAAGA[G/T]TGTGCCTTCTAGGGC | 22992 |
rs116369021 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67184736 | ATTCAGAATAGGAAG[C/T]GACTGCATATGCACA | 22992 |
rs116456689 | snp | C/T | 0.117886 | 0.21224 | intron-variant | KDM2A | GRCh38.p7 | 11:67189557 | AGCAAGACCTTATCT[C/T]GGCCGGGCGAGGTGG | 22992 |
rs116472655 | snp | G/T | 0.0279526 | 0.114869 | intron-variant | KDM2A | GRCh38.p7 | 11:67168248 | TGGTCTTTGGAACTT[G/T]GTAGATGTCCAGTGA | 22992 |
rs116555331 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | KDM2A | GRCh38.p7 | 11:67184150 | GTTGCATCTTCTCCT[A/T]ATTGTTGCAGGCCTC | 22992 |
rs116593365 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | KDM2A | GRCh38.p7 | 11:67189200 | TTTAAAAAATAGATA[C/T]CAAAGTATCTTCTCC | 22992 |
rs116610196 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67241478 | GATTTGGAGCAGGAT[C/T]CTTAGGTTAAGAATG | 22992 |
rs116610720 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67152367 | ACACTTGTTATTCCA[A/G]GTATTTTGCGAGGCT | 22992 |
rs116614858 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | KDM2A | GRCh38.p7 | 11:67136632 | GGCTTCTTGAGAAGG[G/T]GGCATTTTGTACTGA | 22992 |
rs116629110 | snp | A/T | 0.029116 | 0.117091 | intron-variant | KDM2A | GRCh38.p7 | 11:67216127 | TCAGTAGAAATTAGT[A/T]TTCATCTAGTTCACT | 22992 |
rs116711271 | snp | A/C | 0.0372196 | 0.131242 | intron-variant | KDM2A | GRCh38.p7 | 11:67129138 | GTAGGGATGAGGAGG[A/C]TATCTGGATATTGGG | 22992 |
rs116866203 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | KDM2A | GRCh38.p7 | 11:67254061 | CCCAGTGCTCACACC[C/T]TGAAGGCATGGCTGG | 22992 |
rs116903927 | snp | A/G | 0.0142736 | 0.0832652 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255295 | CTGAGGGGAAAGCAC[A/G]GGCTGTGCTGTCGAG | 22992 |
rs116954528 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67240751 | TGAAGGGTGGTGGCT[G/T]CTTTATATGGTTTCT | 22992 |
rs117001685 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67162904 | ATTTTTTAGAGATGG[A/G]GTCTGGCATTGTGTC | 22992 |
rs117006524 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | KDM2A | GRCh38.p7 | 11:67210917 | GAGGCCAAGGTGGGC[G/T]TATCACTTGAGCCCA | 22992 |
rs117023542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67146931 | ATCAAAGGCACATAG[C/T]TTACTGATCTCATTT | 22992 |
rs117044492 | snp | A/G | 0.021333 | 0.101051 | intron-variant | KDM2A | GRCh38.p7 | 11:67167106 | AAAGTTTAATATTGC[A/G]AGTTACTGCTTTTGT | 22992 |
rs117052032 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | KDM2A | GRCh38.p7 | 11:67220413 | GGTGTAATGGGGCTT[A/C]TCAACCCAAATTTCA | 22992 |
rs117266031 | snp | G/T | 0.00318978 | 0.0398085 | upstream-variant-2KB, synonymous-codon | KDM2A, LOC107984341 | GRCh38.p7 | 11:67117711 | TAGTGGAGCCAATAG[G/T]GCCAACCCCGATGTG | 22992 |
rs117279124 | snp | A/C/T | 0.0165278 | 0.0893908 | intron-variant | KDM2A | GRCh38.p7 | 11:67253091 | AAAGAGAACGGAATC[A/C/T]GTGTTGCTGCCAGCC | 22992 |
rs117322901 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | KDM2A | GRCh38.p7 | 11:67245135 | TGTAATCTTCTACCC[A/T]ATCCAGTCTTAAAGC | 22992 |
rs117328678 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | KDM2A | GRCh38.p7 | 11:67247735 | CGGCCAACTTTACAA[C/T]CTTAAAAGTTTGTTT | 22992 |
rs117354215 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67233046 | AAATTATTTTAAGTC[C/T]TTCCTCCTAAGTAAC | 22992 |
rs117393841 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | KDM2A | GRCh38.p7 | 11:67234675 | GCCTGGGCAACGTGG[C/T]GAAACCTCACCTCCA | 22992 |
rs117454425 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | KDM2A | GRCh38.p7 | 11:67222048 | AAATACTCCTGTTTA[A/T]CTCTGTCATTCTTTT | 22992 |
rs117509869 | snp | A/C | 0.0228947 | 0.104514 | intron-variant | KDM2A | GRCh38.p7 | 11:67147900 | GCCAGGCTGTTCTGG[A/C]ACTCCTGACCTCGTG | 22992 |
rs117538255 | snp | C/T | 0.0146672 | 0.084371 | upstream-variant-2KB, missense | KDM2A, LOC107984341 | GRCh38.p7 | 11:67117742 | TAACGCCCCAGCCAC[C/T]GTCCTTTGTGGGATT | 22992 |
rs117598695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67224426 | AGCCTGGACAACATA[A/G]TGAGACCCTGTCCGT | 22992 |
rs117795164 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | KDM2A | GRCh38.p7 | 11:67148482 | AAATAATAGGTATCA[A/G]TCATATCTTTTTTCC | 22992 |
rs117930887 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67145314 | ACATGGTGAAACCCC[A/G]TCTACAAAAAACACA | 22992 |
rs118066315 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | KDM2A | GRCh38.p7 | 11:67237907 | CCTGGGCAACAAAGC[A/G]AGACCCTGTCTGAAA | 22992 |
rs118086134 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | KDM2A | GRCh38.p7 | 11:67174987 | AATCACGTATATGAA[A/G]AGCATCTAGAATAAA | 22992 |
rs118092971 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KDM2A | GRCh38.p7 | 11:67141094 | GGAGTGTCACTCCAC[A/G]TTGTCTCATCGATGA | 22992 |
rs118160633 | snp | A/C | 0.0279526 | 0.114869 | intron-variant | KDM2A | GRCh38.p7 | 11:67236195 | AAGTGCAGTGGCGTG[A/C]TCTAGGCTCACTGCA | 22992 |
rs118173127 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | KDM2A | GRCh38.p7 | 11:67151461 | TCTCTGCTCGCTGCA[C/T]CTTCCGCCTCCCGAA | 22992 |
rs137900530 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67127788 | TCTGGGCTCACCGCA[A/G]CCTCCCTCTCCTGGG | 22992 |
rs137908828 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | KDM2A | GRCh38.p7 | 11:67209565 | TCTCCCACCTCAGCC[A/T]CTCAAATAGCTGGGA | 22992 |
rs137941071 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67174922 | TGTGACACTGGGCCT[A/G]GTGAGGACTGGTACC | 22992 |
rs137982793 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67225194 | TATTTTCACATCACT[C/G]TAGTATACTGACTTT | 22992 |
rs137982881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67167676 | CCTGCTAAATTCTGT[A/G]GACACCTTCTATTTA | 22992 |
rs137984599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67132931 | CTGTGGGTTATAGGT[A/G]GAAATGGAAAGGAAG | 22992 |
rs138021167 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67220699 | TCCTGCAAAGGACCA[A/G]ATAGTAAATATTTTA | 22992 |
rs138022387 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67122370 | TCACTCTGTCGCCCA[C/T]GCTTGGAGTGCAGTG | 22992 |
rs138065693 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67166847 | TTTGGAAGGCCAAGG[A/C/T]GGGCGGATCACTTGA | 22992 |
rs138093913 | snp | G/T | 0.0174175 | 0.0916809 | intron-variant | KDM2A | GRCh38.p7 | 11:67214672 | AGATGGGTTCTCACT[G/T]TGTTGCCCAGGCTGG | 22992 |
rs138105414 | snp | A/C/T | 0.00279242 | 0.0372774 | intron-variant | KDM2A | GRCh38.p7 | 11:67163117 | CTAGTCAGACTGATA[A/C/T]CCAGAATTTTGCTCT | 22992 |
rs138174919 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67186768 | TTGAGAGATCAATAC[A/T]TTTAAAATAATTAGT | 22992 |
rs138199456 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KDM2A | GRCh38.p7 | 11:67241809 | TGCAGTGGCTCATGC[C/T]TGTAATCCCAGCACT | 22992 |
rs138220901 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67162167 | ATTTTGGTTTATTTG[A/G]TAAATCTTCTGTTTC | 22992 |
rs138261684 | in-del | -/ATA/ATC | | | intron-variant | KDM2A | GRCh38.p7 | 11:67168583 | CTTGTATGAATTATA[-/ATA/ATC]CACACACACACACAC | 22992 |
rs138364187 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67203045 | TACACTTCAGCGAAA[A/G]AAAAAGAAGTTGCTA | 22992 |
rs138370035 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67146572 | GGAGTGCAGTGGCAT[A/G]ATCTAGGTTCACTGC | 22992 |
rs138410224 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | KDM2A | GRCh38.p7 | 11:67219180 | ACAAACCACTAAGAA[G/T]CAGAATCAGAGTGAA | 22992 |
rs138442603 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67146084 | GCAACCTCCACCTCC[C/T]GGGTTCAAGCGATTC | 22992 |
rs138458294 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | KDM2A | GRCh38.p7 | 11:67141071 | TCTCAGTTTATCCCC[C/T]TCTCTTTGGAGTGTC | 22992 |
rs138467596 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | KDM2A | GRCh38.p7 | 11:67232801 | CAACCTCCACCTCCC[A/G]GGTTCAAGCAGTTCT | 22992 |
rs138488443 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67227178 | ATGGAACATTAATCT[A/G]GTTTGTGGACATACC | 22992 |
rs138634922 | snp | A/G | 0.000149787 | 0.00865279 | intron-variant | KDM2A | GRCh38.p7 | 11:67253442 | TACATGTCTCATTCC[A/G]TCCATTGCAGGACTG | 22992 |
rs138645118 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67167231 | TCTCTTCAAGATGAT[A/G]TTGAGATGCCTTATC | 22992 |
rs138688996 | snp | A/C | 0.0228947 | 0.104514 | intron-variant | KDM2A | GRCh38.p7 | 11:67132403 | ATTCTCCTGCCTCAG[A/C]CTCCCAAGTAGCTGG | 22992 |
rs138707455 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67179571 | AGGCGTGAGCCACCG[A/C]ACCCGGCCTGGAATG | 22992 |
rs138708477 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | KDM2A | GRCh38.p7 | 11:67128685 | TTTAAGCCCTATTAT[A/T]TTCTGTTGTTTTATT | 22992 |
rs138735027 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67175902 | TCATCTTTTCTAGTT[A/C]TTCAGAGACACATAT | 22992 |
rs138740000 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | KDM2A | GRCh38.p7 | 11:67123026 | CCCAGGGTGACGTTC[A/G]GTGATGTGATCATAA | 22992 |
rs138747307 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67208830 | ACATTTGTAATCCCA[A/G]CACTTTGAGAGGCTA | 22992 |
rs138747659 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | KDM2A | GRCh38.p7 | 11:67142101 | TGGAGTGCAGTGGCA[C/T]GATCTCCGCTCACTG | 22992 |
rs138753050 | in-del | -/TTTATTTA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67187549 | ATTTATTTAATTGAT[-/TTTATTTA]TTTATTTATTTATTT | 22992 |
rs138764535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67204760 | CCTCCCAAAGTGCTG[A/G]GATTACAGGCGTGAG | 22992 |
rs138770192 | snp | C/T | 0.0603597 | 0.1629 | intron-variant | KDM2A | GRCh38.p7 | 11:67157494 | TCACGCTTGTAATCC[C/T]AGCACTTTGGGAGGC | 22992 |
rs138807496 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67207359 | CATTCTTTGTGATTT[C/G]ATTATGATTGTTGAG | 22992 |
rs138837068 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67233742 | GGTACAATGGTATAC[C/G]AAAGGAAAAAGTAGA | 22992 |
rs138898750 | in-del | -/CAG | 0.0785177 | 0.181917 | intron-variant | KDM2A | GRCh38.p7 | 11:67202813 | TGTCGACCCGAGAAA[-/CAG]CGAGATCTTGTATCG | 22992 |
rs138909473 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67136686 | CTTGTGATGTTCAGG[G/T]GTTCTGGGGACCAGG | 22992 |
rs138916622 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | KDM2A | GRCh38.p7 | 11:67225710 | AGAGGCACAGGTTGC[A/G]GTGAGCCGAGATCAC | 22992 |
rs138999330 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67186666 | CCATAGTTTAAGAGA[C/T]GAGCATATTTTTTAA | 22992 |
rs139019872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67182054 | TATCAAAGAGAGTTA[C/T]AGAAGTTGCCTTATT | 22992 |
rs139077511 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | KDM2A, LOC107984341 | GRCh38.p7 | 11:67118596 | GAGCCCAGGTCCCGC[A/G]GGCCCAGCCCGGCGG | 22992 |
rs139087066 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67247933 | TAATCTTCACCACAA[C/T]CCTATAAGGTGGGTT | 22992 |
rs139096606 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | KDM2A | GRCh38.p7 | 11:67164493 | TTTGTTGTTGTTGTT[G/T]TTTTGTAGCGATGGG | 22992 |
rs139117632 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | KDM2A | GRCh38.p7 | 11:67258556 | TCTGCCCGCCTCCAC[C/T]TCCCAGAGTGCTGGG | 22992 |
rs139141837 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | KDM2A | GRCh38.p7 | 11:67153383 | TGTATTCCTCAACCC[A/G]GTTTTTAGACACCCT | 22992 |
rs139143097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67155239 | CAGGCTGGTCTCGAA[C/T]TCCTGACCTCAAGCA | 22992 |
rs139156413 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67252452 | CTCCAGAATAAATCA[C/G]GGTAAAGTGGTCAAG | 22992 |
rs139184798 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67149173 | CCCTTCCTGAATAAA[C/T]TGACTGTTCCCTTAG | 22992 |
rs139186505 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | KDM2A | GRCh38.p7 | 11:67199402 | CCTTTTACATCAAAT[A/G]GTTAACCAAGATGTG | 22992 |
rs139225034 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67201525 | CCTGTAATCCTAGCA[G/T]TTTGGGAGGCCAAGG | 22992 |
rs139228805 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KDM2A | GRCh38.p7 | 11:67222019 | AAAGAAAAAAAATGT[A/G]TAATTCCATAGTAAA | 22992 |
rs139339570 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67228687 | TGAAACCCTGTTGCG[-/A]AAAAAAAAAAAAAAA | 22992 |
rs139349800 | in-del | -/TTTGTTTTGTTTTGT | | | intron-variant | KDM2A | GRCh38.p7 | 11:67198760 | AGTGGTGATCAGTAG[-/TTTGTTTTGTTTTGT]TTTGTTTTGTTTTGT | 22992 |
rs139420331 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | KDM2A | GRCh38.p7 | 11:67158142 | GCAACTACGGATCTT[C/T]TTGCTGTCTGTAGTT | 22992 |
rs139505492 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | KDM2A | GRCh38.p7 | 11:67158848 | TGTTTAGATCTTTTG[C/T]TTACTGTTTTATTGT | 22992 |
rs139524793 | snp | A/G/T | 0.00239393 | 0.0345281 | intron-variant | KDM2A | GRCh38.p7 | 11:67210089 | ATGTAAATAGAAGCC[A/G/T]AGCATGGTGGCTCAT | 22992 |
rs139543449 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | KDM2A | GRCh38.p7 | 11:67229546 | TTACTTTTACTGCAT[A/G]ATTTTACTCATAGTT | 22992 |
rs139607471 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67154707 | GCCTCCCAAAGTGTT[C/G]GGATTACAGGCATGA | 22992 |
rs139616211 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KDM2A | GRCh38.p7 | 11:67243460 | GAGTTTTTCTTTGAC[A/G]TAGTGAGATCATTCT | 22992 |
rs139631145 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67177918 | GGCAACAGTGTCACT[A/G]AGAGATAAGCATTTT | 22992 |
rs139704016 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67147399 | TAAAGAAAATTAGCC[A/G]GGTGTGGTGGCGGGT | 22992 |
rs139742162 | snp | C/T | 0.0685596 | 0.171987 | intron-variant | KDM2A | GRCh38.p7 | 11:67143992 | TGTCGCCCAGACTGG[C/T]GTGCAGTGGTGCAAT | 22992 |
rs139751831 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67236885 | AACTATGCAGACATG[C/T]CGTGGTCCTAGCCCT | 22992 |
rs139758650 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | KDM2A | GRCh38.p7 | 11:67138057 | TGCCTCAGCCTCCCA[A/G]AGTGCTGGGATTACA | 22992 |
rs139776975 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67235303 | TTCCTACTATGAGAA[-/T]TTTTTTTTTTTTTTT | 22992 |
rs139784487 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | KDM2A | GRCh38.p7 | 11:67134256 | CCAAGGAAACATTTA[A/G]CAGTGGACATTTCTG | 22992 |
rs139836956 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67200511 | CGTGAGCGACCGTGC[C/T]CAGCCTGTTTGGTTT | 22992 |
rs139856264 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67195462 | ATTTTTATTTTCTTT[A/T]TAAACTCTTCTATTT | 22992 |
rs139877962 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67254585 | CTTTTTTAACTGATG[G/T]GGGACTGAGGCCTTG | 22992 |
rs139991579 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KDM2A | GRCh38.p7 | 11:67143011 | TTCAGTTATATATAT[A/G]TATCTATTCTTTTTT | 22992 |
rs139997733 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67130551 | TGTTTGTGTTATTCT[C/T]GGGTCTTGGTTTTGG | 22992 |
rs140001390 | snp | A/C | 0.0283406 | 0.115616 | intron-variant | KDM2A | GRCh38.p7 | 11:67216791 | TGGGTGTGGTGGTAC[A/C]TGCCTATAATCCCAG | 22992 |
rs140046013 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67189434 | GCTTTGATTATAAAA[C/T]ACGGAATCACTGATT | 22992 |
rs140049460 | snp | G/T | 0.121022 | 0.21416 | intron-variant | KDM2A | GRCh38.p7 | 11:67177202 | ACCCGGGAGGTGGAG[G/T]TTGCAGAGAGCCGAG | 22992 |
rs140070601 | snp | C/G/T | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67228849 | TCAAGCAATCCCCCT[C/G/T]CTGAGTAACTAGGAT | 22992 |
rs140089756 | snp | A/G | 0.029116 | 0.117091 | intron-variant | KDM2A | GRCh38.p7 | 11:67223131 | TGGGAGGCGGAGGTT[A/G]CAGTGAGCCAAGATC | 22992 |
rs140130777 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | KDM2A | GRCh38.p7 | 11:67215659 | AAAAAAACTTACATT[C/T]TAGTCAATACGGTAG | 22992 |
rs140144804 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | KDM2A | GRCh38.p7 | 11:67225641 | CAGGTGTGGTGGCGC[A/G]TGCCTGTAATCCCAG | 22992 |
rs140170578 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67125310 | GTCAGCTTCCCAGGT[A/G]GCTAGGACTACAGCC | 22992 |
rs140172352 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | KDM2A | GRCh38.p7 | 11:67210607 | GAGAGGGCTCAGAAA[C/T]AGAAAATTATTAAGA | 22992 |
rs140224647 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67180368 | TGCCATTTGCATGCA[C/T]TTATCCCCCAGTCCT | 22992 |
rs140256700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67236961 | AAGAAATAGGAAATA[A/G]GTGCAGTCCAGGTTT | 22992 |
rs140296738 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67145920 | TTCATGAACTGTATC[C/T]GGGAGATTTTCAACA | 22992 |
rs140319931 | snp | A/T | 0.0166325 | 0.0896639 | intron-variant | KDM2A | GRCh38.p7 | 11:67162603 | TAGAGATGGGGTTTC[A/T]CTATGTTGGCCAGAC | 22992 |
rs140382270 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | KDM2A | GRCh38.p7 | 11:67127387 | TGGCTTCCCAAAGTG[C/G]TGGGAGTACAGGTGT | 22992 |
rs140402984 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | KDM2A | GRCh38.p7 | 11:67213582 | GGCCAAGATGGTGAA[A/C]CCCTGTCTCTACTAA | 22992 |
rs140403811 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KDM2A | GRCh38.p7 | 11:67124456 | AGCTGCGATTACAGG[C/T]GCCTGCCACCATGCC | 22992 |
rs140404532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67173682 | GTGTGAGCCACTGCA[C/T]TTAGCCTGGTTTTTA | 22992 |
rs140509398 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67212536 | ATAGACTAGGTTCAT[G/T]ATATTGGACTTCTTA | 22992 |
rs140533552 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | KDM2A | GRCh38.p7 | 11:67232759 | GTCGCTCAGGTTGGA[A/G]TGCAATGGCAAGATC | 22992 |
rs140558115 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67193988 | GCTGAGATTATAGGC[A/G]TAATCTCACTGCACC | 22992 |
rs140591182 | snp | A/G | 0.0726307 | 0.176182 | intron-variant | KDM2A | GRCh38.p7 | 11:67131146 | CCTGGCCAACATGAC[A/G]AAACCCCATCTCTAC | 22992 |
rs140599517 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67255645 | CCTCCTTTCCTCTCC[C/T]TTGAGCTTGGTTCTG | 22992 |
rs140618551 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | KDM2A | GRCh38.p7 | 11:67126107 | CAAAATTAGCCGAAC[A/G]TGGTGACGCATGCCT | 22992 |
rs140639362 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67141023 | TCAAGTCAAAGGTTG[A/G]TAAATACTACTCATT | 22992 |
rs140639424 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67196210 | TCATCCATGGTGCAC[A/G]AGCAGGGGCTTGCAG | 22992 |
rs140690827 | in-del | -/TG | | | intron-variant | KDM2A | GRCh38.p7 | 11:67216463 | AGTTATATTCCAGCT[-/TG]TGTGAAAATGCTTCT | 22992 |
rs140711476 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67190858 | GTTAAGACTAAATCA[C/T]TAAGAAATAGAAAAT | 22992 |
rs140746824 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67144577 | TTTTAATATAAATTT[C/T]TTAGAGACAAGGTCT | 22992 |
rs140829231 | in-del | -/G | 0.00478085 | 0.0486577 | intron-variant | KDM2A | GRCh38.p7 | 11:67205493 | ACAATAGATATAAAT[-/G]TTTTTTTTTCTACAG | 22992 |
rs140900090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67218080 | CAGTGGTTTTCCAAT[A/G]AAGTATATGAGAATT | 22992 |
rs140957364 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67173311 | ATTTTTAGTAGAGAC[A/G]GGGTTTCTCCGTGTT | 22992 |
rs140960382 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67120017 | GAATCTTTTACTTCT[C/T]ACTTGGACAAGAACT | 22992 |
rs140960667 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | KDM2A | GRCh38.p7 | 11:67168860 | TGAGGTTGCTTTTTC[C/T]TTTAAAATGTATTTA | 22992 |
rs140961361 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KDM2A | GRCh38.p7 | 11:67122614 | AGACGTGAGCCACCG[C/T]GCCTGGCCATGGCCT | 22992 |
rs140981702 | snp | A/C | 0.0174175 | 0.0916809 | intron-variant | KDM2A | GRCh38.p7 | 11:67121503 | GGGAAAGGTGTATTA[A/C]TATCGAATTTGGCTT | 22992 |
rs140984427 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206801 | TTTCTCTCCACTACT[A/G]TTTTATGCTGACTCT | 22992 |
rs140998867 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | KDM2A | GRCh38.p7 | 11:67164725 | TCCCAGGGTCAAGCG[A/G]TTCTTCTGCCTCAGC | 22992 |
rs141018889 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67150977 | AGTGTGAGTGGGAGG[G/T]AGTATGTAGTAAACC | 22992 |
rs141020887 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, utr-variant-5-prime | KDM2A | GRCh38.p7 | 11:67186474 | AAGCTAAGGAAACTT[A/G]TTACCACTGGACCTG | 22992 |
rs141075858 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67134949 | TGGTCATGACAATCC[A/T]CAACCCAGTTGCATA | 22992 |
rs141079926 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67224248 | AGATGGGAACATTCT[C/T]AGGAGCTGCATATTC | 22992 |
rs141093719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67202093 | AGACTTCAGTGGAGG[A/G]AGTAACTGCAAATGT | 22992 |
rs141106658 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KDM2A | GRCh38.p7 | 11:67167075 | AGAGCGAGACTCTGC[C/T]TCAAAAAAAAATTAA | 22992 |
rs141201351 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67164393 | AGAAGTTTAACAGAG[A/T]TGTGATTATTAACTT | 22992 |
rs141221024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67215623 | GAGCATACCATAGCA[C/T]ACAACCACACAGTTA | 22992 |
rs141242123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67235946 | CATTTCTAAAATTGG[A/G]AAGTTGTATTCTTGA | 22992 |
rs141310773 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | KDM2A | GRCh38.p7 | 11:67166030 | TGGTGAAGAAACTAG[A/G]CATTATCTTTGTTTC | 22992 |
rs141329683 | snp | C/T | 0.0704125 | 0.17392 | intron-variant | KDM2A | GRCh38.p7 | 11:67249569 | AGTTGGGGGCTCTTG[C/T]GGGATTCCTCACCAT | 22992 |
rs141346637 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67158003 | TAGGTTTCCCTGTTT[G/T]TGTTGTACAGTTCTG | 22992 |
rs141394767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67146497 | CTGTGACAGATTCTC[C/T]CTCTTTGTCTGTCTT | 22992 |
rs141395693 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67241482 | TGGAGCAGGATCCTT[A/G]GGTTAAGAATGAAAA | 22992 |
rs141420937 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67240710 | CCGCACTCCACCCCC[A/G]CTCTCCTATCCCAAA | 22992 |
rs141456221 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | KDM2A | GRCh38.p7 | 11:67140103 | CGGTGGCTTACACCT[A/G]TAATCCCAACACTTT | 22992 |
rs141460311 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67230382 | CCTGTGATCTCAGTA[C/T]TTTAGGAAACCAAGG | 22992 |
rs141491021 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67156592 | GGCGTGGTGGTAGGC[A/G]CCTGTAGTCCCAGCT | 22992 |
rs141493158 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67204881 | TCCTTGTATGGATCA[A/G]CCACATTTTGTTTAT | 22992 |
rs141506039 | snp | C/G | 0.0372196 | 0.131242 | intron-variant | KDM2A | GRCh38.p7 | 11:67202762 | GCCTGGGCGACAGAG[C/G]GAGACTTCGTCTCAA | 22992 |
rs141526438 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67230123 | GGAGCTTGCAGTGAG[C/G]TGAGATGGCACCACT | 22992 |
rs141598059 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67221273 | AGCTTAGCAGAATAC[C/T]AAGCTAGTATGGAGA | 22992 |
rs141631926 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | KDM2A | GRCh38.p7 | 11:67209840 | CTGAGGTGGGAGTAT[C/G]CCTTGAGCCTAGGAG | 22992 |
rs141693021 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67136289 | GTCTCAGATTATCCA[A/G]TTAAGGGACAGAGCC | 22992 |
rs141713945 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67153603 | ATAATCCCAGCACTT[C/T]GGAAGGATTATTTCA | 22992 |
rs141738871 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67181747 | CTGATTGTGAATATT[-/A]ACTGTGTCTGGGGAG | 22992 |
rs141785054 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67204488 | GATACAGTGTGTTTT[C/T]TTTTTTCTTTTTTTT | 22992 |
rs141788520 | in-del | -/CT | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67135381 | GATTTCCTTTTGATA[-/CT]CTCTTTGAAGGATAG | 22992 |
rs141822645 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67192028 | TAAAATTACGGAGAA[C/T]ATCATTAACAAAATG | 22992 |
rs141877613 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67120674 | GGTAGATTTGGGAAT[G/T]ATAAGATCCGGGGAG | 22992 |
rs141887217 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | KDM2A | GRCh38.p7 | 11:67208861 | AGACAGGAGAATTGC[G/T]TGAGGCCAGTAGTTC | 22992 |
rs141890698 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67251856 | TAATGTATAGTGTAT[C/T]TAAATTCTCCTTAAT | 22992 |
rs141920441 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67182258 | GAGTAGAGAAATTTC[C/G]AGGAAATGCTCGCCA | 22992 |
rs142028370 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67176904 | ATGCGAGGGCCTAAG[A/G]CACTTTTGTAGATTT | 22992 |
rs142034313 | in-del | -/ATA | | | intron-variant | KDM2A | GRCh38.p7 | 11:67168580 | AGTCTTGTATGAATT[-/ATA]ATACACACACACACA | 22992 |
rs142042707 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67149052 | TTTTTGCTTCCTTTA[C/G]AGATGGTGGCAGATG | 22992 |
rs142050777 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67246931 | TGTTGAATGAAGAAC[C/T]GGGTTTTTGTTTTGT | 22992 |
rs142075862 | in-del | -/TGTGTG | 0.484632 | 0.086302 | intron-variant | KDM2A | GRCh38.p7 | 11:67201218 | ATATATATATATATA[-/TGTGTG]TGTGTGTGTGTGTGT | 22992 |
rs142236473 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | KDM2A | GRCh38.p7 | 11:67137860 | TGGAGTGCAGTGGTG[C/T]GATCTCGGCTCACTG | 22992 |
rs142243375 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67223890 | ACCAAATACCTATTG[C/G]TTGTTGTCTCTCTCC | 22992 |
rs142272161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67186759 | GTACATAATTTGAGA[A/G]ATCAATACATTTAAA | 22992 |
rs142276518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67212101 | AGGAGTTTGAGGCAG[C/T]CTAGGCAATGTGGCA | 22992 |
rs142296315 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67233509 | ATACAAAAATTAGCT[A/G]GGTGTGGTGGCAGAC | 22992 |
rs142296784 | snp | A/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185331 | TGAACATAGCTTGCT[A/T]TAGGTTAAATGTTAT | 22992 |
rs142315994 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67157092 | GCCGAGAAGGGCCGA[G/T]CACGAGGTCAGGAGA | 22992 |
rs142319176 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67158146 | CTACGGATCTTTTTG[C/T]TGTCTGTAGTTTTGC | 22992 |
rs142390307 | snp | C/T | 0.172351 | 0.237636 | intron-variant | KDM2A | GRCh38.p7 | 11:67155732 | AGCAATTCTCCTGCC[C/T]CAGCCTCCTAAGTAG | 22992 |
rs142409922 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67205751 | CCTCCCAGAGTGATG[A/G]GATTATAGATGTGCA | 22992 |
rs142427113 | in-del | -/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67198317 | TTGCAGATAGTGTAT[-/T]TTTTTTTTTTTTTTA | 22992 |
rs142460358 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | KDM2A | GRCh38.p7 | 11:67203091 | TCAGCAACCACCACC[A/G]CTCTGATCAGTCAGC | 22992 |
rs142494289 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67194456 | TCTTTTCTTAAGTTA[C/T]GTTATCTAGTCAGTT | 22992 |
rs142651947 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | KDM2A | GRCh38.p7 | 11:67160456 | TGACCAGTTTGTTAG[A/G]GAGGAAGCCCTTCAT | 22992 |
rs142693916 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67163206 | CTTCCTTCAAACTCT[C/G]TTGAAGGATCAGCAG | 22992 |
rs142737000 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | KDM2A | GRCh38.p7 | 11:67227237 | GGCAAGCTGAGCATC[A/G]ATAGTGGAGAAAATA | 22992 |
rs142748831 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KDM2A | GRCh38.p7 | 11:67132730 | CTCTTAAGGCAGTGG[C/T]TTTCAAAGTGTAGGT | 22992 |
rs142749126 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67219264 | TGTGTTTTCAGCCAC[A/T]GCCCTCTGTTCCCCT | 22992 |
rs142768892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67129305 | TTTTAAAAGTTTAGT[C/T]TGTCTAGGTACAGTG | 22992 |
rs142788427 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67199112 | ATTACTATTATACTT[C/G]TTTTGAGGTGCCATG | 22992 |
rs142808696 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | KDM2A | GRCh38.p7 | 11:67194030 | TTAGATACTAATCTT[C/G]CCAAAGTTATTTTTA | 22992 |
rs142835968 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | KDM2A | GRCh38.p7 | 11:67225640 | CCAGGTGTGGTGGCG[C/G]ATGCCTGTAATCCCA | 22992 |
rs142888641 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67182884 | TAAAACAAAGGGACT[C/T]TTTAAATTTTCTTCC | 22992 |
rs142912335 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67201897 | GAATTCGAGGTTGCA[A/G]TGAGCTCTGATCTTG | 22992 |
rs142973788 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67130009 | CTGTGGTCACTCAGG[A/C]TGGAGTGCAATGGTG | 22992 |
rs142984190 | in-del | -/AA | 0.172351 | 0.237636 | intron-variant | KDM2A | GRCh38.p7 | 11:67148460 | GTTTTTTCATGGGGT[-/AA]AACTCAAATAATAGG | 22992 |
rs143005744 | snp | A/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67198002 | AAAGTAAGATAAAAA[A/T]TCCTTAAATCATAAA | 22992 |
rs143036584 | in-del | -/TGT | 0.00835141 | 0.0640778 | intron-variant | KDM2A | GRCh38.p7 | 11:67221307 | GCAGATGTGGAGAAA[-/TGT]TAACAGTTGGAGAAT | 22992 |
rs143040502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67215102 | TCCATTTTGACTAGT[A/G]CTGTCTTTACTATTA | 22992 |
rs143054801 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67232372 | TATGCTGGGTTAACG[C/T]TGAGTAGCTTTAGCC | 22992 |
rs143092698 | snp | A/G | | | intron-variant | KDM2A | GRCh38.p7 | 11:67141920 | GAGTGAGAACACGTG[A/G]TACTTCTCTTTCTGT | 22992 |
rs143100501 | snp | C/G | 0.0205511 | 0.0992634 | intron-variant | KDM2A | GRCh38.p7 | 11:67140349 | CCATCCTGGGTGACA[C/G]AGTGAGATCTTGTCT | 22992 |
rs143109242 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KDM2A | GRCh38.p7 | 11:67198243 | ACTTTGACCATCACA[A/G]TTTTATCTAAGTGCT | 22992 |
rs143119774 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67157706 | GCTGAGATGGCGCCA[C/T]TGCACTCCAGCCTGG | 22992 |
rs143135493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67173368 | CTCAGGTGATCCGCC[C/T]GCCTTGGCCTCCCAA | 22992 |
rs143215664 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67169249 | GTGAGCCACTGCACC[C/T]GGCCTAATCCATGTA | 22992 |
rs143230371 | snp | G/T | 0.0376037 | 0.131863 | intron-variant | KDM2A | GRCh38.p7 | 11:67197306 | AGCTTCCTGAGTAGC[G/T]GGGACCACAGGTGGG | 22992 |
rs143289332 | in-del | -/TTTTGTTTTG | 0.079617 | 0.182947 | intron-variant | KDM2A | GRCh38.p7 | 11:67235605 | CGCGCCCGGCTGCTT[-/TTTTGTTTTG]TTTTGTTTTGTTTTG | 22992 |
rs143311639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67196008 | CTTATCTCAGAACCA[C/T]AAGAATTGCTAAATT | 22992 |
rs143412349 | in-del | -/A | | | intron-variant | KDM2A | GRCh38.p7 | 11:67210338 | TTGTTTCTACTTTTG[-/A]AAAAAAAAAACAAAA | 22992 |
rs143418233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67146342 | TAAGAAATAATACAC[C/T]GATTGTCTTTTTACT | 22992 |
rs143452376 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67167650 | CAAGAGACTTAGGTA[C/T]GCATAAGCTTCCTGC | 22992 |
rs143513642 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67175297 | GGCCAGGTGTGGTGG[A/C]TCACACCTGTAATCC | 22992 |
rs143523373 | snp | C/T | | | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67186195 | ACCCTCACCAAGACA[C/T]ATTATAATCAAACTT | 22992 |
rs143541998 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67203876 | TGCGATCTTGGCTCA[C/T]TGCAACCTCTGCCTC | 22992 |
rs143551526 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | KDM2A | GRCh38.p7 | 11:67132065 | TACATTGGTGAAGGC[C/T]TCCTTCAGGTAGGTA | 22992 |
rs143553880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67168147 | TCTTATTAATAAGGA[A/G]ATACTGATAAATCTA | 22992 |
rs143574720 | in-del | -/AC | | | intron-variant | KDM2A | GRCh38.p7 | 11:67145325 | CCCCGTCTACAAAAA[-/AC]ACACACACACAAAAT | 22992 |
rs143590904 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67177525 | CAGCCTGCAGAGGGT[C/T]GGGGTCATCAGTATC | 22992 |
rs143597843 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67253236 | AAGTCACTCCTTCTT[A/G]TATTGCTCTGGTGGG | 22992 |
rs143623795 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67179245 | TATTGATGGTGTGCT[A/G]TTTGGAATGCTGGGT | 22992 |
rs143630813 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67211447 | GGTGAAACCCCGCCT[C/T]TACTAAAAATACAAA | 22992 |
rs143638903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67244592 | AAGGGCTAGGACAAG[A/G]GCTGGTAAATTTTTC | 22992 |
rs143642280 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67121242 | TCTTTAGTGTTGCAA[C/T]CTGGTTCCTAAGGAG | 22992 |
rs143645264 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67152428 | GACAACAGAGCAAGA[A/G]ACCTCATCTCTACAA | 22992 |
rs143648231 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67251502 | CTGGTATATATTTAC[A/T]CTAGGATATATCCTT | 22992 |
rs143736741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67229022 | CCACCACTCCTGGCC[C/T]GGTTGTCTAATGCGT | 22992 |
rs143741017 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | KDM2A | GRCh38.p7 | 11:67172860 | ATCTTAGGGGGAGAG[C/G]TTTCAGTCTTTCACC | 22992 |
rs143756686 | snp | A/G | 0.000200985 | 0.0100226 | missense, intron-variant | KDM2A | GRCh38.p7 | 11:67240208 | GGACTGCCCTGCCCT[A/G]TGTGCTCTGGGAGAT | 22992 |
rs143907851 | snp | C/G | 0.0376037 | 0.131863 | intron-variant | KDM2A | GRCh38.p7 | 11:67153269 | GATTACAGGTGTGAG[C/G]CACTGCACCCGGCTG | 22992 |
rs143927693 | snp | C/T | | | intron-variant | KDM2A | GRCh38.p7 | 11:67146788 | GTGCTGGTGCATGAG[C/T]CACCGTGCCTGGAAC | 22992 |
rs143956262 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67220758 | TAACTGTTTAACCCT[A/G]CCTTGTAGCATGAAA | 22992 |
rs143994120 | snp | A/G | 8.28521e-05 | 0.00643577 | intron-variant | KDM2A | GRCh38.p7 | 11:67215808 | TTTGGTGGGGCAGAT[A/G]TACTTTTTTCCATCA | 22992 |
rs143995658 | snp | A/C/T | 0.0035302 | 0.041865 | intron-variant | KDM2A | GRCh38.p7 | 11:67254200 | CTTCTCTTGCCTGTA[A/C/T]AGGTCAGGACAATCG | 22992 |
rs144015171 | in-del | -/TTG | 0.00835141 | 0.0640778 | intron-variant | KDM2A | GRCh38.p7 | 11:67236710 | AAAATATCTGTGAGA[-/TTG]TTGTTAAAATTAACA | 22992 |
rs144066374 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67149267 | ACAGGGTACTTCTTA[A/C]CCTTTCTGAGTCTCA | 22992 |
rs144067451 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | KDM2A | GRCh38.p7 | 11:67248567 | AGCATTGTGTTTTGT[A/G]TTACTAAATGTTGTT | 22992 |
rs144086900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67223253 | TTAGAAATTGATATG[C/T]GGCATAAGTAAAAAG | 22992 |
rs144093571 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67148536 | CCGGGCGTGGTGGCT[C/T]ATGCCTGTAATCCCA | 22992 |
rs144180132 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67185518 | CCTGTAATCCCAGCT[A/G]CTTGGGAGGGCTCAG | 22992 |
rs144208307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67222647 | ACTTCCCAGTAGGGG[C/T]GGCCGGGCAGAGGCG | 22992 |
rs144261445 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67187187 | AAAGGAATTTACACA[A/T]TTCACCAAATAAATG | 22992 |
rs144336818 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67205448 | CTGATACATCCAGCC[A/T]GGGCAGGTGTTTGTT | 22992 |
rs144345115 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | KDM2A | GRCh38.p7 | 11:67133244 | AGCTGGGATTACAGG[C/T]GTGCGCCACCACACT | 22992 |
rs144349021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67220846 | AGTTGAATTTCAGAT[A/G]ACTTTAACATGTCAC | 22992 |
rs144376125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67143061 | AATCTTGCTCTTGTC[A/G]CACAGGCTGGAGTGC | 22992 |
rs144412576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67139832 | CTTCTGCCTCAGGTC[C/T]TGAGTAGCTGGGATT | 22992 |
rs144438938 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | KDM2A | GRCh38.p7 | 11:67254018 | GAGAAGAAAGAAAAC[G/T]TGTCTGGTTTCCTAG | 22992 |
rs144747082 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67126858 | CAGAATATTCTGCAG[C/T]GTTGGAGTGGAACAG | 22992 |
rs144761392 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | KDM2A | GRCh38.p7 | 11:67213160 | ACATCTGGGTATCCT[C/G]TAGACAACTGCTTCA | 22992 |
rs144780237 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67159464 | AAGATTAGATTCATC[C/T]TAAACATTTTGGCAA | 22992 |
rs144785794 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67122993 | TATTTTTATTTTTAT[A/T]GACAGGATCTTGCTC | 22992 |
rs144792174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67208055 | AAATAAAATGCGTTG[C/T]TTTTATACTGGGAAA | 22992 |
rs144798503 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67176708 | GCATGTTACAGTACT[A/G]AATACTATAGGCAGT | 22992 |
rs144818958 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | KDM2A | GRCh38.p7 | 11:67226240 | CTAGCCTTGGTGACA[C/G]AGCGAGATTCCATCT | 22992 |
rs144907064 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67140113 | CACCTATAATCCCAA[A/C]ACTTTGGGAGGCTAA | 22992 |
rs144920685 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | KDM2A, LOC107984341 | GRCh38.p7 | 11:67120060 | CTCCGGTGAGTTTCC[C/T]CCTCCCCCCCCTCAT | 22992 |
rs144959250 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KDM2A | GRCh38.p7 | 11:67164788 | ATTTTTAGTGGAGGT[A/G]GGGTTTCACTATGTG | 22992 |
rs144996973 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KDM2A | GRCh38.p7 | 11:67140109 | CTTACACCTATAATC[C/T]CAACACTTTGGGAGG | 22992 |
rs145004969 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67230932 | ACCAAAACTTCAGAC[A/C]AAAAAAAAAAGTTTT | 22992 |
rs145019390 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67134319 | AATGAGTAGAGGCTA[A/G]GGATGCTGCTAAAGC | 22992 |
rs145026344 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KDM2A | GRCh38.p7 | 11:67223500 | CTCAACCTCGTAGGC[G/T]CAAGTGATCCTTCTG | 22992 |
rs145096441 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KDM2A | GRCh38.p7 | 11:67190401 | GGTGACAAGAGCAAA[C/T]CTCCGACTCAAAAAA | 22992 |
rs145116167 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KDM2A | GRCh38.p7 | 11:67186647 | TAACTCCTTTTTGTT[C/T]TCTCCATAGTTTAAG | 22992 |
rs145118240 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | KDM2A | GRCh38.p7 | 11:67249995 | CTTTCTTCTCTCTGG[A/T]CCCCTGAGAGCAAGG | 22992 |
rs145187619 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67125535 | CCATCACTTTGGGAG[A/G]CATAGGCAGGAGGAT | 22992 |
rs145207794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM2A | GRCh38.p7 | 11:67187854 | GCTGGGGATTATAGG[C/T]GTGAGCCATGGCACC | 22992 |
rs145275671 | in-del | -/AATCTTAA | 0.119978 | 0.213528 | intron-variant | KDM2A | GRCh38.p7 | 11:67244526 | GCTCAGGGAGGGGTG[-/AATCTTAA]CAGCTCTGCAAAAAG | 22992 |
rs145318301 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KDM2A | GRCh38.p7 | 11:67236886 | ACTATGCAGACATGC[C/T]GTGGTCCTAGCCCTC | 22992 |
rs145336870 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | KDM2A | GRCh38.p7 | 11:67206297 | TTAGGCAGGCGTGGT[G/T]GCACACGGCCATATT | 22992 |
rs145392517 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | KDM2A | GRCh38.p7 | 11:67196742 | GGACTTAAAACGGCC[A/C]TAGTTTCAGTTTTAT | 22992 |
rs145412681 | snp | A/G | 0.0142736 | 0.0832652 | utr-variant-3-prime, nc-transcript-variant | KDM2A | GRCh38.p7 | 11:67257212 | GAAATTTCCAAGCCA[A/G]TGGTTTCTTTTGGGT | 22992 |