SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs137936762 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46038730 | TGGCTAAGCATGCTA[A/G]CATACTTGCTCAGGT | 51317 |
rs137946119 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | PHF21A | GRCh38.p7 | 11:45943184 | CCGGAGTGCAGTGGC[A/G]CAATCATGGCTCACT | 51317 |
rs137963804 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46092803 | TACTCTGTTGTCCAG[A/G]CTCAAGTGCAGTGGC | 51317 |
rs138028302 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46068358 | GGGAATAAATGGGAA[G/T]GGATTTTTTGAAAGC | 51317 |
rs138029116 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46098783 | GAGCTTATTTTGGTG[C/T]ACAGGGATTTAAGGA | 51317 |
rs138030745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46035058 | AGAGGTTTGCTGCTT[C/T]TTGCATTCCTGAGGG | 51317 |
rs138064031 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46084972 | GGCGTGAGCCACTGC[A/G]CTGAGCCAAAATCAT | 51317 |
rs138071819 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45973525 | GCCATTGCCTCCTTA[A/T]ATGTGAAATGAGAGT | 51317 |
rs138078414 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | PHF21A | GRCh38.p7 | 11:45983486 | TATACATGTCTGTTG[C/T]TATCTGTGAAAAAAA | 51317 |
rs138087702 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PHF21A | GRCh38.p7 | 11:46022806 | CTTTTTTTTTGAGAC[A/G]GAGTCTCGGTCTATT | 51317 |
rs138098779 | snp | A/G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930266 | GCGTGCTGCAGACAC[A/G/T]GTCACCCTCACGGAA | 51317 |
rs138105706 | in-del | -/C | 0.00438332 | 0.0466095 | intron-variant | PHF21A | GRCh38.p7 | 11:46081211 | CCAACCATGGGACCT[-/C]CCAAATACACAAGGT | 51317 |
rs138180002 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46003576 | TGACATTTTCACGAA[A/G]GGCAGAGTGAGAAAA | 51317 |
rs138232116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46020384 | CCAAGAACCAGGAGC[A/G]CCTGCTCTGACACTG | 51317 |
rs138242314 | snp | C/T | 0.00350372 | 0.0417083 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934201 | TCTGCCGGGCCAGGA[C/T]GGTGTTCTTCATTTC | 51317 |
rs138297435 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | PHF21A | GRCh38.p7 | 11:46100213 | ATGCTAGCCTTTAAG[A/T]CCAAAAATATGTTAT | 51317 |
rs138298718 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | PHF21A | GRCh38.p7 | 11:45976632 | GGATCACTTGAGCTC[C/T]GGAGTTTGAGACCAG | 51317 |
rs138319583 | snp | A/G | 0.00943836 | 0.0680448 | intron-variant | PHF21A | GRCh38.p7 | 11:45953661 | AAAAATTCAGAATTC[A/G]TTTTTTATTAAAAGG | 51317 |
rs138320256 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | PHF21A | GRCh38.p7 | 11:46066399 | AAAATTAATATGTGT[C/T]CCTTATAAAAAATAA | 51317 |
rs138334566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45968118 | AAGTGCCTAGCATAG[C/T]ACCTAGTATGTAGCA | 51317 |
rs138395319 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45955285 | TCTTTCTCTCTCCAA[A/C]ACACACACACACACA | 51317 |
rs138405072 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46061231 | GTATAGTTTGAAGTC[A/G]GTTAGCATGATGCCT | 51317 |
rs138421329 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | PHF21A | GRCh38.p7 | 11:46040253 | AACATAATGGTCTCA[C/T]CTCAGTGGAAAAGAG | 51317 |
rs138428861 | in-del | -/AAAA | | | intron-variant | PHF21A | GRCh38.p7 | 11:45958397 | CAAAACCTGGTCTCA[-/AAAA]AAAAAAAAAAAAAAA | 51317 |
rs138433415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45944602 | CCCCGCTATCCTGGC[C/T]CTCTTGCTTTTCTTT | 51317 |
rs138448690 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | PHF21A | GRCh38.p7 | 11:45998013 | AGTTTTGCTCCTATC[A/G]AAACATTTCAGTACC | 51317 |
rs138455095 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | PHF21A | GRCh38.p7 | 11:46046548 | TCACTCTGCTTTTTT[A/C]ATGGTTATTAGAAGC | 51317 |
rs138488447 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PHF21A | GRCh38.p7 | 11:46052397 | ACCAATAAATCTCTT[C/T]TCCTTCAACAACATT | 51317 |
rs138575818 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46001493 | AAGCTCCAGTTGGTG[A/T]CTCCGTCACATGCAC | 51317 |
rs138625045 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | PHF21A | GRCh38.p7 | 11:46033980 | CAATTTTATATTCCA[C/T]TCAGCAGTGTATAAG | 51317 |
rs138645045 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:45977485 | AACAGGATGTTTCCA[C/T]GGGTTAAGACAGAAA | 51317 |
rs138646542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46086149 | TTTGAGAAAGAGTCT[C/T]GCTCTGTCGCCCAGG | 51317 |
rs138654557 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46015374 | GTCAATTTTTGTTTT[C/T]GTTACAATTACTTTT | 51317 |
rs138700816 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46021398 | ACCTCACCACATTTT[A/T]AACTATTAACAAGTA | 51317 |
rs138708023 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46117479 | TTTGCAGGCTAACTT[A/G]AGTACATCAACCATA | 51317 |
rs138727043 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:45985222 | TGCATTGATAAGTCA[C/T]ACCAATATTCATCAA | 51317 |
rs138728130 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46072467 | AGAGCAACAGAATAG[A/G]AGGAACCTGGGTTCC | 51317 |
rs138744457 | in-del | -/AGT | 0.0952156 | 0.196321 | intron-variant | PHF21A | GRCh38.p7 | 11:45991260 | GTCTGAATGTATCAC[-/AGT]AGTAGTACCTTGATT | 51317 |
rs138748109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45959862 | CAACAGAAAAATAAC[C/T]CAATTTAAAAATTGG | 51317 |
rs138752537 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | PHF21A | GRCh38.p7 | 11:46054327 | AATCATTAACTCTGA[A/C]AAACTAACAACATAC | 51317 |
rs138766919 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46077910 | CCCTAAATCTAATTT[A/G]TTATTTATTTATTTA | 51317 |
rs138821722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46071065 | GGTAGATGAATTACT[A/G]TTTTCAATTTCCATA | 51317 |
rs138827729 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | PHF21A | GRCh38.p7 | 11:45973111 | TAAAAATAAAAACTA[A/T]ATTAATTAAATGTAA | 51317 |
rs138843746 | snp | C/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45953576 | GCAGGTGGGGTGATG[C/G]TGCGGCTCTCTGTTT | 51317 |
rs138853591 | snp | C/T | 0.0146672 | 0.084371 | downstream-variant-500B, utr-variant-3-prime | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45929079 | ATCCCTTTTTCATAA[C/T]TAAAGTTTTAAAACA | 51317 |
rs138905214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46045937 | AGTTCACAACTGGCT[C/T]TGTTTTCTTGCTTAC | 51317 |
rs138906772 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45935842 | AGGTATTTTCCCCAG[A/C]GCTCCCATGAGTCCT | 51317 |
rs138917819 | in-del | -/GTAT | | | intron-variant | PHF21A | GRCh38.p7 | 11:45987274 | ATGTATGTATGTATG[-/GTAT]TATGTATGTAACCTG | 51317 |
rs138989186 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PHF21A | GRCh38.p7 | 11:46101777 | AATAGCTGGGACTAC[A/G]GGCACATGCCACCAC | 51317 |
rs138997291 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | PHF21A | GRCh38.p7 | 11:45998633 | TTCTCCTGCCTCAGC[A/C]TCCCGAGTAGCTGGG | 51317 |
rs139011099 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45957226 | TAAGTAATGGATAAA[A/C]CTTGTGCAGAGATTA | 51317 |
rs139020268 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PHF21A | GRCh38.p7 | 11:46073032 | ATCCTGTTAAATAAA[C/T]TAATAGTTGCTTCCA | 51317 |
rs139023576 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PHF21A | GRCh38.p7 | 11:46110172 | GTAATATAAAGTACA[C/T]TCATGAGTATTATCT | 51317 |
rs139060012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46057409 | CAGGAGTGTTAATTC[A/G]ATACATATAACAGAT | 51317 |
rs139068892 | snp | A/G | 0.00478085 | 0.0486577 | upstream-variant-2KB | PHF21A, LOC105376661 | GRCh38.p7 | 11:46123152 | GAGCAACAGTGGTGA[A/G]ATGATTTGCCCAAAG | 51317 |
rs139077166 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46011857 | TCTCTCTATGCAACA[C/T]AACAAAACAAAAAGA | 51317 |
rs139097770 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46067389 | AGTGACGTAGTAACA[A/T]TGCAGAAGAGACTTG | 51317 |
rs139102461 | in-del | -/AC | 0.0314385 | 0.121371 | intron-variant | PHF21A | GRCh38.p7 | 11:46097826 | ATCTCCCTAACTAGA[-/AC]ACACACACACACACA | 51317 |
rs139141045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46016465 | TTTGCCTTTGCTTAA[A/G]TTATTCCCTCTCTCA | 51317 |
rs139162091 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46010389 | ATCTTGTGAAGATAC[C/T]TTACAGAAGAATAAC | 51317 |
rs139290675 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46096483 | CAATGATTTAACAGT[G/T]GTTAAATCCAACAGA | 51317 |
rs139291696 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:45993147 | ATTTAATTTACATGA[G/T]TAAGAAAAAACAATT | 51317 |
rs139311048 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:45940870 | GGATAAACGAAGAGG[C/T]GTTCACTTTCCTTTG | 51317 |
rs139376022 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | PHF21A | GRCh38.p7 | 11:45964027 | ACATGGAGAAACCCC[A/G]TCTCTACTAAAAATA | 51317 |
rs139396631 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | PHF21A | GRCh38.p7 | 11:46088435 | CAACAACAACAACAA[A/C]AAAACATAAAAACCA | 51317 |
rs139414158 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45932774 | TAAAAAAACAGTGCC[C/T]GAACGATGACACAAG | 51317 |
rs139437635 | snp | C/T | 0.000406532 | 0.0142513 | synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45965351 | GCTAAGCTGTACAGT[C/T]TGAGGTCCAGCGAGT | 51317 |
rs139467692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46113344 | GCACACAGTTTCTCT[A/G]GCACATACCGGAAAA | 51317 |
rs139477838 | snp | C/G | 0.000153988 | 0.00877328 | missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45933984 | TATTTAGTCTCTTCC[C/G]CCTGGTTACAGTTCG | 51317 |
rs139485291 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PHF21A | GRCh38.p7 | 11:46007184 | CCATGTGTTCAAAAA[C/T]ATGCAAAGTGATAGT | 51317 |
rs139491575 | snp | C/T | 9.93526e-05 | 0.00704744 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45965458 | CATTGACGACACGGA[C/T]GGGGTGGATGGAATT | 51317 |
rs139496223 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46036935 | AGGCTAGTCTTGAAC[G/T]CCTGGCCTCAGGCAA | 51317 |
rs139522384 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PHF21A | GRCh38.p7 | 11:46023302 | GGCTAATTACTGAGG[C/T]CCCTTCTATTTTGAA | 51317 |
rs139545173 | snp | A/G | 0.00795532 | 0.062565 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45931910 | GGAGAGGCCACAACC[A/G]GCCAAGCCGAGGCAA | 51317 |
rs139562439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46042390 | ATGTGTGATAGTGCA[A/G]CTCCGGAAAGTTCAT | 51317 |
rs139575416 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | PHF21A | GRCh38.p7 | 11:46104039 | CATAGGTAGCTTATG[A/G]CAATTAAATATAGAA | 51317 |
rs139643495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46112737 | TCCATCCAACCTTAC[A/G]GAACAACTATCCCCA | 51317 |
rs139691690 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PHF21A | GRCh38.p7 | 11:45955099 | CCACTGGTGTTCTCT[C/T]GTATTTCCCCCTTTA | 51317 |
rs139731828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46104817 | CAGCACAGTGGTATG[C/T]AGCACGTATGTGATA | 51317 |
rs139741980 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45988014 | GACAAGTTGGATATG[A/C]AAATACAATTTAAGT | 51317 |
rs139743387 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | PHF21A | GRCh38.p7 | 11:45946469 | GCTCACTGCAACCTC[C/T]GCCTCCCGGGTTCAA | 51317 |
rs139761891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45991598 | CACTTTTTCTCCTCC[A/G]CTCTGCTTTTAGAAA | 51317 |
rs139838896 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PHF21A | GRCh38.p7 | 11:45970125 | CTTCTGTTTCCTCCT[A/G]CACCTAATGGAGAAC | 51317 |
rs139871532 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PHF21A | GRCh38.p7 | 11:45965217 | ACAATGGTGGTGAGA[C/T]GAAGAGCCCTTGAGA | 51317 |
rs139927266 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:46055005 | TTGCTAATCTTGTAA[C/T]ACAGGACCAGGCTTT | 51317 |
rs139997788 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PHF21A | GRCh38.p7 | 11:45979449 | AAGTGTAAATAAATA[C/T]CTCCAAAAATTCAAA | 51317 |
rs140012226 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | PHF21A | GRCh38.p7 | 11:46088924 | ACTCGAAGGAAAGCT[A/G]TAACTCCAATTTTAC | 51317 |
rs140019026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45988223 | GAAGAGGTAAATATA[A/G]CAGATTATTTAACCA | 51317 |
rs140045105 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46094763 | AAATTAGCTGGGTAT[A/G]GTGGTGTGCACCTGT | 51317 |
rs140067410 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PHF21A | GRCh38.p7 | 11:46030457 | AATGGGGGCTAATAT[C/T]AGATTTCAATACCAG | 51317 |
rs140133973 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46061706 | CAACCTAAACTGGCT[-/G]GTTTTCTAAACCTGT | 51317 |
rs140142221 | snp | C/G | 3.35864e-05 | 0.00409781 | synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45969842 | GTTTGGACGTGGAGT[C/G]AGTCTAGGAGGGGGG | 51317 |
rs140147881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45950852 | TGTTTCACTTGTCAC[A/G]ACTAGGTCAGTTTCT | 51317 |
rs140158336 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | PHF21A | GRCh38.p7 | 11:46045487 | CACTACTATTACTCC[A/G]GTCTAATTACTTGCT | 51317 |
rs140164173 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PHF21A | GRCh38.p7 | 11:45940217 | TTTTTTTTTTTAGAC[A/G]GAGTCTCTTGCTCTG | 51317 |
rs140182277 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45945314 | TTTGTGGGTGAAGGG[C/T]TACTAAGTATTTGAC | 51317 |
rs140229376 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | PHF21A | GRCh38.p7 | 11:45956625 | CTAGATTGTTAAAAA[C/T]GTATGAATGTTTACT | 51317 |
rs140269085 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46114531 | TCACCATAAAAGTGA[C/T]GGGCTACTATAAAGG | 51317 |
rs140273453 | snp | C/G | 0.0887219 | 0.191022 | intron-variant | PHF21A | GRCh38.p7 | 11:46007498 | TTTGTATTTTTAGTA[C/G]AGATGGGGTTTCACC | 51317 |
rs140287025 | snp | A/T | | | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46085905 | CAGGGCTTATATACT[A/T]GATTATATAACATCA | 51317 |
rs140291263 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | PHF21A | GRCh38.p7 | 11:45983476 | CGTGTGTGGTTATAC[A/G]TGTCTGTTGCTATCT | 51317 |
rs140344426 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | PHF21A | GRCh38.p7 | 11:46089765 | ATGTCTGAATGTATG[A/T]GAGTATAAAATATCT | 51317 |
rs140345318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46026997 | ATGTAGGAAAAGGAA[C/T]CCTTTTCTGAAAAAT | 51317 |
rs140350720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46080254 | GCCTTAACCTCCTGG[A/G]CTTAAGTTATCCTTC | 51317 |
rs140358721 | snp | A/G | 0.00636936 | 0.0560724 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45929617 | GGACCCACGGACACC[A/G]GAGAGAGGTGAGGGT | 51317 |
rs140368358 | in-del | -/ACAC | 0.00478085 | 0.0486577 | intron-variant | PHF21A | GRCh38.p7 | 11:46046746 | GCTTTCTACATGTAA[-/ACAC]ACTATAAAACCCAAC | 51317 |
rs140375900 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46000066 | TCGATTGACTAGAGA[G/T]CTGAGGACAGTACAT | 51317 |
rs140418275 | in-del | -/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46052259 | AGCTGCCAGAGGCAA[-/C]CCTCTGCCAGTACAG | 51317 |
rs140442729 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | PHF21A | GRCh38.p7 | 11:45976338 | CAAAATTTCTCTACA[A/T]CTTAAATTTTTTTAA | 51317 |
rs140445879 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:46076224 | TCTCCTGCCCTATAT[A/G]GAATAAGTCTAATAA | 51317 |
rs140539278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46069788 | CAATGATGCACTTGT[A/G]ATTGAGTTAAATGTT | 51317 |
rs140543084 | snp | C/T | 0.000153988 | 0.00877328 | missense, synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934131 | TTGGAGAGGTCGATG[C/T]CGTGGATGAGGCGAA | 51317 |
rs140552281 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46062221 | GGCACTCAGTGGATT[C/G]TATTAATCTGGAATT | 51317 |
rs140571781 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | PHF21A | GRCh38.p7 | 11:46013044 | TGAACCCTATATATA[A/C]TATGTTTTTTCCTAT | 51317 |
rs140584709 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46032052 | CAACTCTTAAGTGCT[A/G]CTTTAAAAAGAAAAC | 51317 |
rs140584829 | snp | A/G | 0.02016 | 0.0983543 | intron-variant, downstream-variant-500B | PHF21A | GRCh38.p7 | 11:45934744 | ATTTAGGAGGATCGA[A/G]GCCCCAAGGACAAAG | 51317 |
rs140660193 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | PHF21A | GRCh38.p7 | 11:46115665 | ATTAATATTTCCCAG[A/C]ACAAAATAATATGAA | 51317 |
rs140667299 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:46050654 | ACAATGTTCAAGAGC[A/G]TAGTCCAAGATCCTG | 51317 |
rs140669905 | in-del | -/AAACA | | | intron-variant | PHF21A | GRCh38.p7 | 11:45975384 | AATAAAATAAAACAA[-/AAACA]AACAAAATAAAATAA | 51317 |
rs140683385 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PHF21A | GRCh38.p7 | 11:45958226 | AAATTCCAGAAAATA[C/T]ACTCTTAAATCATTC | 51317 |
rs140783129 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46004721 | GAGGGCTGTATCTGC[C/T]AGGCCTAGAATGCTT | 51317 |
rs140790005 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45957223 | CTTTAAGTAATGGAT[A/T]AAACTTGTGCAGAGA | 51317 |
rs140795845 | snp | A/C/G/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46098834 | ATGGGAGTTCTGGGT[A/C/G/T]TAAACCATAAGCACC | 51317 |
rs140807470 | in-del | -/TTTTC | 0.275464 | 0.2487 | intron-variant | PHF21A | GRCh38.p7 | 11:46087549 | TTCATTTGAAATTCT[-/TTTTC]TTTTCTTCAGAAAGA | 51317 |
rs140815940 | snp | A/G | 0.119978 | 0.213528 | intron-variant | PHF21A | GRCh38.p7 | 11:46033408 | CAGCTGGGACCACAG[A/G]TGTGCACCACCACAT | 51317 |
rs140867833 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PHF21A | GRCh38.p7 | 11:45955971 | TAAACTTGTGAAGGA[C/T]TATCAGCCAGAACTA | 51317 |
rs140870481 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PHF21A | GRCh38.p7 | 11:46059189 | TTTACGTCCAAGGAT[A/G]TACACTGCAGAGCTA | 51317 |
rs140876547 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:45962517 | CTGCTGATCGGGCTC[A/G]GTAACCTCTAAGACT | 51317 |
rs140899666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46081057 | TAATTTTAAAAAGAC[A/G]AGTGAATAGGTTGTA | 51317 |
rs140924091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46026113 | CTATTCGTACTTAGG[C/T]GAGAGACCTGGGCTA | 51317 |
rs140949919 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46116824 | AAAACTTAGCCGGGC[A/G]TAGTGGCGGACACCT | 51317 |
rs140955136 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | PHF21A | GRCh38.p7 | 11:45973007 | CACTTGAACCCGTGA[A/G]GCAGAGGCTGCAGTG | 51317 |
rs140971307 | snp | C/T | 3.29506e-05 | 0.00405884 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45979886 | TTTGTTTTCAGATTG[C/T]GGCAATGGCTGTATT | 51317 |
rs140988085 | in-del | -/TCAAGCAATCTTCTCACT | 0.0123036 | 0.0774623 | intron-variant | PHF21A | GRCh38.p7 | 11:45980610 | CTTGAACTCCTGGCA[-/TCAAGCAATCTTCTCACT]TCAGCATCCCAAGTA | 51317 |
rs140989370 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | PHF21A | GRCh38.p7 | 11:46074906 | CCTTCAAGTATTAGC[C/T]TACCTAAAAATGATA | 51317 |
rs141013358 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | PHF21A | GRCh38.p7 | 11:46077141 | AGTATCCATTGACAG[A/C]AAACCCAAAGCTCCA | 51317 |
rs141044234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46107569 | AAGGCTTTAGCACTT[C/T]GTGGATCTAAAGAAG | 51317 |
rs141049547 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46065158 | TGTTTAGGTATCTAG[C/T]TTCCAAATGCTCAAG | 51317 |
rs141060827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45965952 | CAATAGCCTTAACTC[A/G]CATTTGAAATTTCTT | 51317 |
rs141117857 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | PHF21A | GRCh38.p7 | 11:46091746 | AGAGATGAGGGTCTC[A/G]TTTTGTTGCCAGCTT | 51317 |
rs141129808 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46097511 | AATCTACAGCAGTTT[C/G]AGGAGCAAAAGAATA | 51317 |
rs141146711 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | PHF21A | GRCh38.p7 | 11:46028999 | TTTCTATTGGATCTA[C/T]AAATTGTACCACAAG | 51317 |
rs141164476 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45995027 | GACCTGGGAGAAAGA[C/T]CTAATTGTCAGACTG | 51317 |
rs141244643 | snp | C/T | 0.00713967 | 0.05932 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45933932 | TTCTGTTCTCCTTGC[C/T]GCCGGGATCCCGTGG | 51317 |
rs141266857 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PHF21A | GRCh38.p7 | 11:45968496 | CACCCTGGAACTACA[C/T]ACATGTTCTGTCCTC | 51317 |
rs141270001 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45982693 | CAGTCCTCCTCCCCA[A/T]CAGACATCAAACATA | 51317 |
rs141271625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46067414 | GACTTGTTTCTAGAT[A/G]TATCAAGTTTTCAAA | 51317 |
rs141280786 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PHF21A | GRCh38.p7 | 11:46083607 | GCCTGATGTCCAGCT[A/G]AAGTCTAGAAAGATA | 51317 |
rs141311911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46043781 | AGATGAGAGGACCCC[A/G]CTGTCATATACCCAC | 51317 |
rs141357666 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | PHF21A | GRCh38.p7 | 11:46001650 | TTTTTAAAATTCCAT[C/T]AGTATCTTGCCAGAT | 51317 |
rs141388105 | snp | A/C/G/T | 0.000348898 | 0.0132036 | missense, utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934062 | GCATTGGCAGGGGGG[A/C/G/T]TGCAGTCCGGGCCAT | 51317 |
rs141411613 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:45942142 | TTATCTTAAAAATAC[C/T]TTCTGCTGAGTTTAA | 51317 |
rs141416262 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PHF21A | GRCh38.p7 | 11:46060710 | TTCCATATAGATGCT[A/G]GATATTAGACCTTTG | 51317 |
rs141426845 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45984457 | CTTCAAGTCACAGTT[-/T]CCAAGACAGGTAGTC | 51317 |
rs141450248 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PHF21A | GRCh38.p7 | 11:45947842 | GCCCAGGAATCAATA[C/T]AAAGCCATGACTTAG | 51317 |
rs141500467 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46088156 | GGCTACATTTGTAAA[A/G]GATGATTTAACATAT | 51317 |
rs141554262 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46002381 | TGCTTCAGAAATAAA[C/T]TAATTTGTAACTTTA | 51317 |
rs141554888 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46072726 | TCCTCTGAGGAAGTG[A/T]CATTTAAGCTATGAC | 51317 |
rs141555989 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | PHF21A | GRCh38.p7 | 11:46019774 | TAAACAGTAGCTCTG[A/C]TCTAAAAATGATAAC | 51317 |
rs141622916 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46079675 | GTTCGGTGCAGGGGA[A/G]GATAAGTTCAGTGGG | 51317 |
rs141626720 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | PHF21A | GRCh38.p7 | 11:45944348 | GAGAAGCATAGGCAA[A/C]ATGTTAACAACTGAT | 51317 |
rs141651690 | snp | A/C/T | 0.000202158 | 0.0100519 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45965362 | CAGTTTGAGGTCCAG[A/C/T]GAGTCTGGTCCCTGG | 51317 |
rs141686809 | in-del | -/AGCCT | 0.219648 | 0.248151 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45932148 | AGGGCTGATGCAGCC[-/AGCCT]GTACTCCCGCACCCT | 51317 |
rs141736945 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | PHF21A | GRCh38.p7 | 11:46014447 | TTCCATGTCTTTGCT[A/G]CTGTGAATAGTGTGG | 51317 |
rs141740169 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PHF21A | GRCh38.p7 | 11:45972343 | ATGGCCTAAACATCT[A/G]TCTGGAGATAGATCA | 51317 |
rs141741491 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PHF21A | GRCh38.p7 | 11:46021406 | ACATTTTAAACTATT[A/G]ACAAGTATACACCAT | 51317 |
rs141805772 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:45966820 | GACAGGGTTTCACCA[C/T]GTTGGCCAGGATGGT | 51317 |
rs141843673 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46009570 | CTATGTATTACATAA[C/T]TTAATCTTCAAAGCA | 51317 |
rs141886876 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | PHF21A | GRCh38.p7 | 11:46078060 | GGCCTTACAAGGCAC[C/T]CATCACCATGCCTGG | 51317 |
rs141917492 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46103163 | TGATTTTCAAAATTG[C/T]ATAATTCTTTAACTC | 51317 |
rs141932535 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45939345 | TAGGGGGAGTTTAGA[A/C]GGACTGGGAAAGAAG | 51317 |
rs141940654 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | PHF21A | GRCh38.p7 | 11:46035918 | AGCAAAGAGAAGACA[A/C]AGAGAGGTTTTAAGC | 51317 |
rs141957836 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46038906 | GATTAAGTTTCCAAC[G/T]CATGAAACTTGGGGG | 51317 |
rs141969672 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46043941 | TTAAATTATATACTT[A/T]ATGATTTATATCAAG | 51317 |
rs141975302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45958713 | TTGAGTCCACGAGTT[C/T]GAGACCAGCCTGGGC | 51317 |
rs141987571 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45999861 | TATATAGAAACATCG[-/T]TAACTTTTCTCTTGA | 51317 |
rs142022508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46094226 | TTATCTCCAAGGCAT[C/T]TTCTCCAAAAATGAG | 51317 |
rs142085006 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45975362 | TAAAATAAAATAAAA[C/T]AAAATAAAATAAAAT | 51317 |
rs142138238 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46045967 | CAGAGATAAAGTACC[A/G]TATTAAAACTCAATA | 51317 |
rs142142808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46037772 | TGAGAACTTGAACAA[C/T]ACTTGAAAATTTTAG | 51317 |
rs142161748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45994085 | AATGATATACTTCCT[C/T]GTCTACATAGTATGA | 51317 |
rs142204723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45945760 | CAAGAAGGTGCAAGT[C/T]GATAAGGAGACAACA | 51317 |
rs142234118 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PHF21A | GRCh38.p7 | 11:46056518 | GCTTTTAAAAAATAG[A/G]TCCTTGTAAACGTCT | 51317 |
rs142241310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45961268 | ATGAAGTTAATCAAG[C/T]ATACTTTATATACTT | 51317 |
rs142243135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46097399 | ACTGGCCTCTTTTCC[A/G]TACTTCAGACCCTCC | 51317 |
rs142264427 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | PHF21A | GRCh38.p7 | 11:45992942 | GCTACCTCAAGTGGT[G/T]GAGAAAGCAGTTGTT | 51317 |
rs142275648 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:45976034 | CTTAGACTTCCCTAT[A/G]ACTGTTAAAAAACCC | 51317 |
rs142280118 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46041030 | TGAACATGCCTCTAC[A/C]GTAAATAGGTCGCCC | 51317 |
rs142280119 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PHF21A | GRCh38.p7 | 11:46110426 | GTCAAAGGTCTCTAT[A/G]CTGAATCTACATGGC | 51317 |
rs142366586 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46048253 | ATAAACAGAATCATA[C/G]AGTATAAGGCCTTTT | 51317 |
rs142404612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45971543 | CATACTCCTTACTAC[A/G]GAGAAAGGCAATCTC | 51317 |
rs142411689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46069257 | AAACGAGGAGCTGAT[A/G]TCCTCTGATGTACAC | 51317 |
rs142413568 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45932205 | CGCACCACAGAGCTC[C/T]GCTGGCCAGTTCCCT | 51317 |
rs142434954 | in-del | -/AT | | | intron-variant | PHF21A | GRCh38.p7 | 11:46108577 | GTGTGTATATATATA[-/AT]TATATATATAAAATA | 51317 |
rs142503675 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46118226 | TCTTTTTCATCTATT[A/C]CTACTCCAGTTCCAC | 51317 |
rs142518869 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PHF21A | GRCh38.p7 | 11:46018597 | GCCTTTTAAATCCCA[C/T]TAACCTATTTGACTC | 51317 |
rs142519594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46064386 | AGAGCAAAGGAATGT[C/T]TGGTGCTTCACTGAG | 51317 |
rs142562959 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | PHF21A | GRCh38.p7 | 11:45973539 | AAATGTGAAATGAGA[C/G]TAAACGCGGAACACT | 51317 |
rs142590467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46090191 | GAGCATAGTGACAAT[A/G]AGGCCAAGGTTTTAG | 51317 |
rs142607836 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:46013503 | AAGCCACAGAAATGG[A/G]AACTGCAGGTAAGTG | 51317 |
rs142627161 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:45969440 | CTACTAGTTGGTTTA[A/G]CTGTTGTTTCCTTCC | 51317 |
rs142656020 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45966195 | TCTATGTACTGAAGA[C/T]TCACACTTTTACCTC | 51317 |
rs142697763 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45990579 | TTCATCTTCTTCCAG[C/T]ATACTCCTAAGTACT | 51317 |
rs142717960 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | PHF21A | GRCh38.p7 | 11:45936153 | CATGGTAGTACACAC[C/G]TATAGTCTCAGCTAT | 51317 |
rs142722491 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | PHF21A | GRCh38.p7 | 11:46006046 | AAAACAGTCTTTGTA[A/G]ATAAAAAATAATTCA | 51317 |
rs142730304 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PHF21A | GRCh38.p7 | 11:45986032 | GTATTGATTAGACTT[C/T]GGCTTACTTTTTTAA | 51317 |
rs142744198 | in-del | -/AGAG | | | intron-variant | PHF21A | GRCh38.p7 | 11:45996512 | CCCTTTTTGAGAGAC[-/AGAG]AGAGAGAGAGAAACG | 51317 |
rs142747504 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PHF21A | GRCh38.p7 | 11:46083216 | ACTTAAAGAAGCCCA[C/T]GTGCATAGGGCCAAC | 51317 |
rs142774916 | snp | A/T | 0.000543895 | 0.0164819 | intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45946051 | AACGGGGAGGGAAAG[A/T]GAGGGGGAAAATGAT | 51317 |
rs142787547 | in-del | -/CT/CTCCCT | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:46121177 | CTCCTCTCTCTCTCA[-/CT/CTCCCT]CTCACTCTCTCTCTC | 51317 |
rs142787919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46046623 | ATATATTTCCCTCAT[A/G]TATCTTCTCTGTCAA | 51317 |
rs142813888 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PHF21A | GRCh38.p7 | 11:46112387 | CTGCTAATTCTAAAC[A/G]TTTACTGAGCCCTTA | 51317 |
rs142817626 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PHF21A | GRCh38.p7 | 11:46005315 | AAATATTGTATAAAA[C/T]TTATACAAATTTATG | 51317 |
rs142948382 | snp | C/T | 0.000382896 | 0.0138312 | missense, utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934054 | AGGTGGCGGCATTGG[C/T]AGGGGGGGTGCAGTC | 51317 |
rs142973301 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45959980 | AAATGCACATCAACA[C/G]TACTTTGCACCCACT | 51317 |
rs142998426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46014194 | TGGAGTCCCTAGTGT[C/T]TACTGTTCCCATCTT | 51317 |
rs143008374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45949559 | ATTGTTTTATCTATT[A/G]GTTTTCCCATAAGAA | 51317 |
rs143011014 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46085348 | ATATAATGGCATGTG[A/G]AGATAATGTCAAAAG | 51317 |
rs143014906 | snp | A/G | 0.209997 | 0.246779 | intron-variant | PHF21A | GRCh38.p7 | 11:45962669 | GGCCAAGGCAGGTGG[A/G]TCGCCTGAGGTCAGG | 51317 |
rs143098668 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:46052411 | TTTCCTTCAACAACA[C/T]TGAATTGAGTTTCTA | 51317 |
rs143099814 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46106581 | TTTCAATAATTTGCA[C/T]ATATCCAACTCCATC | 51317 |
rs143124439 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PHF21A | GRCh38.p7 | 11:46007470 | AGGTGCCCACGACCA[C/T]GTCCAGCTTATTTTT | 51317 |
rs143124534 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PHF21A | GRCh38.p7 | 11:46068802 | CCAGCACCAAAAATA[A/C]GTTATTAGGATAAAC | 51317 |
rs143124954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45941797 | TTTGCTAGGCGCTGA[A/G]GACGTATGTTTTTAG | 51317 |
rs143141110 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | PHF21A | GRCh38.p7 | 11:46117839 | TTATACTATCCGCAA[C/T]CGCACATCTACTTTG | 51317 |
rs143149900 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:46010516 | TTTCTTTCTGCTTTA[C/T]GACATTGTTTGGGAA | 51317 |
rs143175909 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46028424 | CAAACATATTACTTT[A/C]ATAATTAGAATAATA | 51317 |
rs143190838 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46011629 | TGCTTTTCATTTCTA[A/T]ATTCAAGAAACAGTT | 51317 |
rs143194121 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | PHF21A | GRCh38.p7 | 11:45995448 | CACAGCATGTTTGTG[-/T]TGACAGTTATACTGT | 51317 |
rs143281579 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | PHF21A | GRCh38.p7 | 11:46021269 | GTCTCACTCTGTTGC[C/T]CAGGCTGGTCTTGAA | 51317 |
rs143304095 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45968228 | ATTTATTCTCTGCAC[A/C]GAGGCAAGAAGGAAT | 51317 |
rs143319716 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | PHF21A | GRCh38.p7 | 11:46065070 | GAAAGTGTTATAGAG[A/T]CAGACATTGTTAACT | 51317 |
rs143414540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46059764 | CAGAGTCTCACTCTG[C/T]TGCCCAGGCTGGAGT | 51317 |
rs143429437 | snp | C/G/T | 0.00795532 | 0.062565 | intron-variant | PHF21A | GRCh38.p7 | 11:45995214 | TGGGATACAGTGGAA[C/G/T]GAACCCACTCATCAG | 51317 |
rs143434210 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PHF21A | GRCh38.p7 | 11:45983622 | GCAGAGGTGCTCCTT[A/G]GGTGTGGAGGCCCTG | 51317 |
rs143521159 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | PHF21A | GRCh38.p7 | 11:46050185 | TCCTTTTTTCCCCCC[A/T]TAATTTGGCCTAGGC | 51317 |
rs143532389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45989123 | ACTGATTAACTTCAT[A/G]GAATTGGCTCTTCCA | 51317 |
rs143552365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PHF21A | GRCh38.p7 | 11:45934874 | AAAGAGAGGAAAGAG[A/G]TGTTAAATCTGCATG | 51317 |
rs143561777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46035746 | GTGTCTCAGAAGGGA[A/G]ACCAGTAAGTTCAAA | 51317 |
rs143570530 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | PHF21A | GRCh38.p7 | 11:45934300 | CCCCTAAGAGCAGAG[C/T]GCCTTCTCTCTGCCC | 51317 |
rs143591811 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46078156 | GAAGTTTCTCACGGA[A/C]GTAGGATCATTCAAA | 51317 |
rs143613093 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:45940489 | GTGAGCCACTGCGCC[C/T]GGCAGATTTTAATGT | 51317 |
rs143629966 | snp | C/T | 0.00128444 | 0.0253095 | missense, utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45979776 | TGTGAAGCAGTCAGG[C/T]TGGGAGAGGCTGCAG | 51317 |
rs143650781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46055217 | AGATCTCTTACCCAA[A/G]TATAACAAAGCAGCA | 51317 |
rs143699900 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46071660 | CACATCTAGGAATTT[A/C]TCCTAAGACCATCAG | 51317 |
rs143733112 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | PHF21A | GRCh38.p7 | 11:46014250 | ACTCCCACTTATAAA[A/T]GAGAACATATAATAT | 51317 |
rs143745708 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:45958357 | AGCTTGAGCTCAGGG[G/T]TTCAAGACCAGCCTG | 51317 |
rs143746782 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46088986 | ACAGAAACCTTTTTC[C/T]AATCAAAACTTGACT | 51317 |
rs143843072 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46008883 | CACTACTTATTTGAC[C/T]AGTGTTCACCCTCCA | 51317 |
rs143878034 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45931043 | GCTGGGTTGCATCTC[A/G]TACTCCATACTAGCT | 51317 |
rs143881073 | snp | C/G | 1.68499e-05 | 0.00290253 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45969853 | GAGTGAGTCTAGGAG[C/G]GGGGATAAACTGTGG | 51317 |
rs143931086 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46061557 | GCTTGGTTTTCTATA[G/T]TCCTACAATTAATTC | 51317 |
rs143945395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45937896 | ATGAGGCACACTGGA[C/T]TTTAAAGGGTCTTGA | 51317 |
rs143948529 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | PHF21A | GRCh38.p7 | 11:46073699 | TGTATACTCTCACTT[A/G]TTATTTCAGAGCACA | 51317 |
rs143956160 | snp | A/G | 0.030665 | 0.119967 | intron-variant | PHF21A | GRCh38.p7 | 11:46017066 | ACCTCTGCCTCCCAG[A/G]TTCCAGCGATTCTCC | 51317 |
rs143980683 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | PHF21A | GRCh38.p7 | 11:45961926 | AGAGCCACAGTGTAA[C/T]GTGGTTTCTAATAAG | 51317 |
rs144001145 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | PHF21A | GRCh38.p7 | 11:45964398 | TAAGGTCTAGTACCC[A/T]ATGCATAGGTTCCTC | 51317 |
rs144012954 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46080597 | TTAAAGTTCTTAAAT[C/G]CACATTGTAGTTTTC | 51317 |
rs144058995 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | PHF21A | GRCh38.p7 | 11:46011987 | GATGACTATCACCTT[C/G]TTTACTTCCTGTCCA | 51317 |
rs144146541 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46119583 | TTAGAAATCACTCTC[A/G]GCACATCTGCACCCG | 51317 |
rs144154266 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PHF21A | GRCh38.p7 | 11:46011451 | GAGCGGAGATGGTGC[C/T]ACTGCACTCCAGCCT | 51317 |
rs144182111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46042662 | TAATCCCCAGTGCAA[C/T]TGTATTATGAGGTGA | 51317 |
rs144195995 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PHF21A | GRCh38.p7 | 11:45982253 | TAAGCCACCACGCCC[A/G]GCTGAGAGGTTTTTA | 51317 |
rs144203123 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PHF21A | GRCh38.p7 | 11:45988047 | AGTGATGATGCTAAA[C/T]TGGAGGAGGGGAAAG | 51317 |
rs144216894 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46047401 | TAAGGTATTTTATAA[A/T]TTTTTTTTATTAGTT | 51317 |
rs144251438 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PHF21A | GRCh38.p7 | 11:46088906 | TTCATTACGATTCTA[A/G]TAACTCGAAGGAAAG | 51317 |
rs144262108 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45975357 | TAAAATAAAATAAAA[C/T]AAAATAAAATAAAAT | 51317 |
rs144289321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46111530 | GTTTTCTTAAATAAA[C/T]ATGGTAGCCCTCAGC | 51317 |
rs144297315 | in-del | -/A | 0.0260105 | 0.111035 | intron-variant | PHF21A | GRCh38.p7 | 11:46081391 | CCACAGTCTTCAATG[-/A]AAAAAGCTCTTGATT | 51317 |
rs144307982 | in-del | -/AG | | | intron-variant | PHF21A | GRCh38.p7 | 11:45996512 | CCCTTTTTGAGAGAC[-/AG]AGAGAGAGAGAGAAA | 51317 |
rs144322527 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46040386 | AGACAATAAAAGTTT[C/T]TTTTAGCATTCTTTA | 51317 |
rs144322699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46037173 | TAATTCTGACTAATT[C/T]GGTGCACATCCCTAC | 51317 |
rs144363809 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PHF21A | GRCh38.p7 | 11:46104206 | CTCTGGGGTTCTACA[A/G]TTGTTTCCACTAGTT | 51317 |
rs144437609 | snp | A/T | 0.0248432 | 0.108648 | intron-variant | PHF21A | GRCh38.p7 | 11:45947043 | TGACAAACATCCTGA[A/T]AAACTACATCTCTAA | 51317 |
rs144495709 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46023993 | TCACTGAATGGCATA[C/G]AGCATGTAGCAACCT | 51317 |
rs144558820 | in-del | -/TTCT | | | intron-variant | PHF21A | GRCh38.p7 | 11:45969502 | GAAGTGTTAATTGCA[-/TTCT]TTCCCCACTGCCAGG | 51317 |
rs144566788 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45994642 | AGAGTGGTTATGTTT[C/T]AGGCTTTGTAAGAAC | 51317 |
rs144597372 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:45978003 | TTAGTTTTCTCTTCT[-/A]AAAAACAGAGATGGT | 51317 |
rs144598265 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | PHF21A | GRCh38.p7 | 11:45977595 | AGAGAACAACCTAAC[A/C]CAATTCTGTTTAAAA | 51317 |
rs144616740 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PHF21A | GRCh38.p7 | 11:46062376 | TCTTAAAATTTTTCT[C/T]TATTCTACTGTCTAT | 51317 |
rs144643799 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | PHF21A | GRCh38.p7 | 11:45963561 | AAGCACCTTCTACAA[C/T]TTATATTTTTGTAAT | 51317 |
rs144659872 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46059221 | GCATACAACAGTAAA[A/C]AACTGGGAATAATTT | 51317 |
rs144681640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45954470 | CTGTCTATATAATCC[A/G]TCAGAGGAGAGATGC | 51317 |
rs144727394 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45971959 | AAGGATTAGCATGTC[C/G]CCTCTGAGGTAGTTA | 51317 |
rs144737441 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46054661 | CTGTTGAGAAAAATC[A/G]TTACTATTCAAATCA | 51317 |
rs144748969 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46077411 | TCAAAAAAAGAATAC[G/T]ATTTTAGATGAGATA | 51317 |
rs144759713 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45991554 | ACAGCTGCAGTAAGC[G/T]TATACACACACACAC | 51317 |
rs144768762 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PHF21A | GRCh38.p7 | 11:46093245 | CTCCACTATATGCTA[C/T]GCTCTAAAACTACAT | 51317 |
rs144784051 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:45982859 | AACATAAACATGACA[C/T]CTGCCAAAAAATAAA | 51317 |
rs144784888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46024145 | GATTTTATATGTTGG[A/G]CTAACTGAGTTGCTG | 51317 |
rs144925907 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | PHF21A | GRCh38.p7 | 11:46036232 | ATTGTGGTAGACTGT[C/G]GTAAAATTTACAGTC | 51317 |
rs144966202 | in-del | -/T | 0.0142736 | 0.0832652 | intron-variant | PHF21A | GRCh38.p7 | 11:46068013 | AATCAGGTAAAAAGG[-/T]TAAGAAAATTCCAGG | 51317 |
rs144966693 | snp | C/T | 0.000924455 | 0.0214796 | synonymous-codon, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934034 | GGGGGAAGGGGCCGG[C/T]GTGGAGGTGGCGGCA | 51317 |
rs144974596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46018928 | GCAAGACTTTTTATG[A/G]CAAAATCAATGTATC | 51317 |
rs144976266 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46081105 | CCTTTAGTAAAATGT[A/C]TAATCTTTGGTGTAT | 51317 |
rs145019364 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PHF21A | GRCh38.p7 | 11:46097019 | ACTCCACATCTACTC[C/T]GACAGCCAACCATGT | 51317 |
rs145068383 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PHF21A | GRCh38.p7 | 11:45949292 | CTTCACAGAACTGGC[C/T]AAGTACAATCAGGGT | 51317 |
rs145092584 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46109153 | TTTGGACATTTAAGA[C/G]CAAGGGCTCAGGAAT | 51317 |
rs145093641 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | PHF21A | GRCh38.p7 | 11:46001731 | GGGAGAATAAAACCA[A/G]TAAGAAACCTTTCTG | 51317 |
rs145113140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45951559 | TTGAAATGACATACA[C/T]TTTGTGGTTGCCAAC | 51317 |
rs145167196 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46100866 | GGGAGCACATAGCAA[C/G]TTTCTAACCACTGTT | 51317 |
rs145172014 | snp | A/C | 0.000153988 | 0.00877328 | missense, utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934093 | TGGAGATGGCCCCCA[A/C]AGTGGCCTCAGAGTC | 51317 |
rs145192247 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | PHF21A | GRCh38.p7 | 11:46049020 | TGTCTGTTAGGGAAT[C/G]GCTAAACTAGCTCTG | 51317 |
rs145217025 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45955123 | CCCTTTATACTAAAC[A/G]CTATGTAAGAGTGGG | 51317 |
rs145226218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46076405 | GGCTTTAAGACAGGT[A/G]ACAAGGTACACGCAG | 51317 |
rs145246824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45941447 | CATCACACATCATGC[A/G]ATATCTGGTAAACCC | 51317 |
rs145255856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45961017 | CATTTTCTATTGTCA[A/G]TTATTATCATGCTTG | 51317 |
rs145288953 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46105136 | AGGCAGAGCAGGAAG[A/T]CATTTGGCCACAGTC | 51317 |
rs145306787 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | PHF21A | GRCh38.p7 | 11:45962599 | TTAGACCAAAAAGAA[C/G]AGAGAACATTGGCCA | 51317 |
rs145321178 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46113077 | TTAGAGGGCTGGGAA[C/G]CTGTGTATAATAAAA | 51317 |
rs145322248 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46043906 | CAGAAAACAGTAAAA[G/T]ATGGATCGCAGCAAC | 51317 |
rs145328083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46115470 | GAAAACATAAGCTAT[C/T]TAAGAAATAATTATC | 51317 |
rs145351106 | snp | C/T | | | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46085904 | TCAGGGCTTATATAC[C/T]AGATTATATAACATC | 51317 |
rs145396887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45956743 | CAAACAAAAAAGGCA[A/G]TATTACAGGAAATGA | 51317 |
rs145400983 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46027252 | GCTAACAGGTACAAC[A/G]TGAACAGGCCAAGGA | 51317 |
rs145405707 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | PHF21A | GRCh38.p7 | 11:46030933 | AGAGAAATTGCTGAT[C/T]TTAAAACAGTAGCAT | 51317 |
rs145407885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46013479 | GCCTCAGCTGACCGT[A/G]AGTAACTAAAGCCAC | 51317 |
rs145439289 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45956598 | AAAAATCTAAGCTGG[A/G]GTTAATTCAAACTAG | 51317 |
rs145465811 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PHF21A | GRCh38.p7 | 11:45973514 | TTATTCTCTTTGCCA[C/T]TGCCTCCTTAAATGT | 51317 |
rs145467937 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46032665 | TGAAAAGGCTATATA[A/T]ACTTTCATCAATAGA | 51317 |
rs145477372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46049989 | ACCATATTCTATCAT[A/G]TATTTCATGTAGTCA | 51317 |
rs145509780 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46074393 | GATAAGGTAATTCAG[A/C]TTTTAGTTATTAAAG | 51317 |
rs145519514 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:45970491 | AATTTAGATATATTT[A/C]TCCCAAGCTTCTGAG | 51317 |
rs145522756 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | PHF21A | GRCh38.p7 | 11:46114125 | CATCCCCACACACAC[A/G]CGCTTCTACAAAGAA | 51317 |
rs145583555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46043761 | TGTCTGCATCTCCCA[C/T]TCAGAGATGAGAGGA | 51317 |
rs145616055 | in-del | -/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46067590 | AATAAGAATATTCCA[-/C]CCCCCCACAAAAAAA | 51317 |
rs145691748 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46015592 | CAGCTTAAAACACAT[C/T]GTACAGTTGTATAAA | 51317 |
rs145708413 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | PHF21A | GRCh38.p7 | 11:46070372 | GTCTCACTGTGTTGC[C/G]CAGGCTGGAGTGCAG | 51317 |
rs145712083 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | PHF21A | GRCh38.p7 | 11:45972503 | AATTAATTGGCCAGG[C/T]GCAGTGGCTCACACA | 51317 |
rs145738714 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:45984512 | AGCGATACTATCAAC[A/G]TGTTCACACGACAGC | 51317 |
rs145743770 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | PHF21A | GRCh38.p7 | 11:45976499 | TTTTGGCAGGGACCA[C/G]TGCTCTTTGTATACC | 51317 |
rs145749596 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45988440 | GCCTTACATTTAAAC[A/G]AAAGTAACACTTGTA | 51317 |
rs145770442 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | PHF21A | GRCh38.p7 | 11:46051504 | TCCTTCTGGGGCCTC[C/G]AGAGATAAATGGGTT | 51317 |
rs145831781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46008073 | GGTGAAAATTAACAC[A/G]AAGTGAAGTTCAGAA | 51317 |
rs145865564 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45980533 | GATAGTGTCTCTCTA[A/T]ACTGCCCAGGTTGGA | 51317 |
rs145901883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46116686 | ACAAAAATTTAGGCC[A/G]GGCGTGGTGGCTCAC | 51317 |
rs145903197 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46039392 | TAAATCAATATATGC[A/G]TGGCTGTAAAAAGTC | 51317 |
rs145926527 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46099209 | CACAGTAAACCCAAC[-/T]ATAGCCAGAAGCTTA | 51317 |
rs145950672 | snp | C/G/T | 0.0150874 | 0.0857668 | intron-variant | PHF21A | GRCh38.p7 | 11:46064776 | ACAATTTTTAAATAC[C/G/T]AAAAAATTAAAAAAT | 51317 |
rs145992986 | in-del | -/ATTTTATG | | | intron-variant | PHF21A | GRCh38.p7 | 11:45940655 | TTTTCTTCCTTCATT[-/ATTTTATG]ATTAAAATCAGGCTG | 51317 |
rs146028864 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PHF21A | GRCh38.p7 | 11:45969707 | AATGTTTAGCTAAGC[A/G]GGATAGACAGCTGGG | 51317 |
rs146029891 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46068787 | AAGTCATTCCATTTG[C/G]CAGCACCAAAAATAC | 51317 |
rs146033545 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:46072184 | TTCCCAGTATTTATT[A/T]CCCAATTCTTACTCA | 51317 |
rs146039628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45974578 | CCCATCTCATTCTCC[C/T]GAGTACCTTGGACTA | 51317 |
rs146048858 | in-del | -/A | 0.0267878 | 0.112589 | intron-variant | PHF21A | GRCh38.p7 | 11:46012775 | GGCCTGCTTAAGGCC[-/A]AACTCATTGTCTTCC | 51317 |
rs146113428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45945264 | TTTGTTGAGGTTCAT[C/T]TAAACATTTAGAGCA | 51317 |
rs146151805 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:45991826 | ATATCTTTACCTCTA[C/T]AGCACTGCACAGAGA | 51317 |
rs146162606 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45940056 | CCTCCACCACCACTA[A/G]TGAAGGAACACATCG | 51317 |
rs146172290 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46072862 | ACAGTAACAAGCAAC[A/T]AACTTCGGAATGTTA | 51317 |
rs146214688 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46068803 | CAGCACCAAAAATAC[A/G]TTATTAGGATAAACT | 51317 |
rs146235374 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:45968775 | TCTCTACTAAAAATA[A/C]AAAAATTAGCCGGGC | 51317 |
rs146265929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46016119 | TAATGTATTACGCTA[C/T]CAAGTAGTTATGATG | 51317 |
rs146271727 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46010375 | TATACCTCGCAACAA[C/T]CTTGTGAAGATACTT | 51317 |
rs146271761 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:46070943 | CACTTATTATCAATA[C/T]ATGCTATTAATGTGA | 51317 |
rs146290538 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45974424 | CAAACGACAAATTAT[A/T]ATTATTATTATTATT | 51317 |
rs146291627 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46102848 | AAGGTTTTGATAATA[C/G]CTCAGTATCTCCCTG | 51317 |
rs146306676 | in-del | -/T | 0.00716266 | 0.059414 | intron-variant | PHF21A | GRCh38.p7 | 11:46118377 | CAATGTCAGTCAAAC[-/T]GTAAATACTATTATG | 51317 |
rs146332874 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46095108 | TTTAGACTAATGATT[C/G]TTAAACACTGTGCAC | 51317 |
rs146386346 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46041482 | GGGAAACTAAGGGGT[A/G]ATCTGAAAGTCAGAA | 51317 |
rs146387328 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46013731 | CTATTGCTTATGGGC[G/T]AAACCTAGGAGCAGG | 51317 |
rs146391141 | snp | A/G | 3.29511e-05 | 0.00405887 | intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45946015 | CGACCTATATACCAA[A/G]AGAAGGGAACAAAAG | 51317 |
rs146396740 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46046093 | GATTACCAAACTTAT[C/T]TGAAAGCTGAAGGCT | 51317 |
rs146409559 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | PHF21A | GRCh38.p7 | 11:45964626 | TTTCTCATCACTAGT[C/T]GTTTTTCAAATAGGA | 51317 |
rs146461356 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | PHF21A | GRCh38.p7 | 11:46057926 | TAACTACCAACCTGA[A/C]AGGCACAAATCAAGA | 51317 |
rs146495233 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:46033363 | TCTGCCTCCTAGGCT[C/T]GAGGGATCCTTCCAC | 51317 |
rs146534502 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PHF21A | GRCh38.p7 | 11:45988167 | TGAGATAATGTAGGA[A/G]GTCACATTTTCACAG | 51317 |
rs146575008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46037596 | TGCGGTGAGCCGAGA[C/T]CGTGCCAGCGCACTC | 51317 |
rs146583163 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | PHF21A | GRCh38.p7 | 11:45982372 | TATTCTGCTAGCACT[A/G]CCTCTCTGAGTAAAT | 51317 |
rs146597431 | snp | A/G | 0.000397442 | 0.0140912 | synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45965546 | AAGCTGAGGAGCTGC[A/G]AGCATGGGAGGTGGT | 51317 |
rs146615242 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46059426 | ACCAATCTCAATTTT[A/T]TTTATTTATTTATTT | 51317 |
rs146634008 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45933603 | TCTCCTCCCTCCGCC[C/T]GTCCCTGCTCCCCAC | 51317 |
rs146654582 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | PHF21A | GRCh38.p7 | 11:46011637 | ATTTCTAAATTCAAG[A/G]AACAGTTTTGGTTTA | 51317 |
rs146692322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46065077 | TTATAGAGACAGACA[C/T]TGTTAACTTTCTTGA | 51317 |
rs146696376 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46007496 | TTTTTGTATTTTTAG[C/T]AGAGATGGGGTTTCA | 51317 |
rs146734668 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46084501 | TAAGAAATGAAAAAC[C/T]AAAAAAAGGGTTTAA | 51317 |
rs146775738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46036831 | AGGTCATCTGCAAAT[A/G]ATGATGATATACATC | 51317 |
rs146779650 | snp | C/T | 4.94752e-05 | 0.00497344 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934129 | GTTTGGAGAGGTCGA[C/T]GCCGTGGATGAGGCG | 51317 |
rs146812621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46026827 | CACTCAGCAGAGCCA[A/G]CATCACGAAGAATGC | 51317 |
rs146816431 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PHF21A | GRCh38.p7 | 11:46031989 | TCTTCCACACTAACA[C/T]GAAAACCACAGCTTT | 51317 |
rs146821133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45934336 | GAAGAAGCTCTGCTG[A/G]CTGCTGTGCAGCCCC | 51317 |
rs146855468 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PHF21A | GRCh38.p7 | 11:46115506 | TAAATTCAATGCAAT[A/G]TTAACATATTATCTC | 51317 |
rs146889561 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45971197 | CGTCTGGAGGTTGAC[C/T]GGTGTGTTCTGCACA | 51317 |
rs146891624 | in-del | -/TA/TATATATA | | | intron-variant | PHF21A | GRCh38.p7 | 11:46108567 | AAATGTGTGTGTGTG[-/TA/TATATATA]TATATATATATATAT | 51317 |
rs146922729 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45937126 | CCGCTGCACCACAGG[C/T]TGCAGGATGAGGACA | 51317 |
rs146923855 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | PHF21A | GRCh38.p7 | 11:46098580 | TTCCATAGCTCTCAC[A/G]AAGCTGTTTTCTGAG | 51317 |
rs146924202 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PHF21A | GRCh38.p7 | 11:46034858 | ATGTGACCCTGGCCA[A/C]ACAAATCAAAGTACT | 51317 |
rs146932386 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45942779 | TATTCTGCTGCTCCT[C/T]GGAGAGGGGTGTGCC | 51317 |
rs146960517 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46092016 | AATGCGTTTGAAGTA[C/T]AGCTACGTGAAATTA | 51317 |
rs146968192 | in-del | -/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46101859 | CGTGCTGGTCTCCCT[-/C]TTTTTTTTTTTTTTT | 51317 |
rs147006277 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | PHF21A | GRCh38.p7 | 11:46038525 | CAGTTGTGTGATTAT[C/G]TTTATTAGTTTACTG | 51317 |
rs147021868 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45949000 | TGTGGTTATTACTAA[C/T]ACTGGCACAAGCTAA | 51317 |
rs147038491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45967216 | CTACTAAAAATACGA[A/G]CATTAGCCAGGCATG | 51317 |
rs147110091 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PHF21A | GRCh38.p7 | 11:46065540 | CCTTATTTGAATCAA[C/T]AAATTCACTTACTAT | 51317 |
rs147160942 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PHF21A | GRCh38.p7 | 11:46035827 | AGAAAGAGAGAGAGA[A/G]AAGAGAGGTTGGAGA | 51317 |
rs147175458 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | PHF21A | GRCh38.p7 | 11:45978068 | GCACTTTGGGAGGCC[A/G]AGGCGGGCAGACCAC | 51317 |
rs147266210 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46061669 | CTTAGCTTTGTTTCT[C/G]CTAAGTCCTCCATCC | 51317 |
rs147270171 | in-del | -/AAAAAAAAAAAAAAAAA | | | intron-variant | PHF21A | GRCh38.p7 | 11:46088417 | TCCAATAACAACAAC[-/AAAAAAAAAAAAAAAAA]AACAACAACAACAAC | 51317 |
rs147282132 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PHF21A | GRCh38.p7 | 11:46004213 | TGAATTATGCATACT[A/G]GTAAGAAATTTCATC | 51317 |
rs147308885 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46081030 | ACCTGCTGTGTGGTA[C/G/T]GCTCACTGGACTAAT | 51317 |
rs147378528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46087024 | TCAAACTGAAGACCT[A/G]TAAGATAATAATACT | 51317 |
rs147393274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46005847 | AAAAAGAAACACTTC[C/T]AATGAAATGTGGAAA | 51317 |
rs147406056 | in-del | -/TGTG | | | intron-variant | PHF21A | GRCh38.p7 | 11:46030850 | TGTGTGTGTGTGTGT[-/TGTG]GTGTGTGTGTGTGTG | 51317 |
rs147414161 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PHF21A | GRCh38.p7 | 11:46112397 | TAAACGTTTACTGAG[C/T]CCTTATTATGTGCCA | 51317 |
rs147424018 | snp | A/G/T | 1.65452e-05 | 0.00287616 | PHF21A | 11 | allele_origin=G(germline)/A(somatic) | 11:45934199 | CTTCTGCCGGGCCAG[A/G/T]ATGGTGTTCTTCATT | 51317 |
rs147438481 | snp | A/G | 6.61551e-05 | 0.00575093 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45953580 | GTGGGGTGATGGTGC[A/G]GCTCTCTGTTTGTTT | 51317 |
rs147478433 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46010902 | GTGAACAGCATCATA[C/T]CAGCTCCTTTCTCTC | 51317 |
rs147482023 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45954859 | GGCTACATGAGACTT[C/T]GGTCCTACAAACAAG | 51317 |
rs147483002 | snp | C/T | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46118886 | GCTGACCTATTTATT[C/T]CTATTGCTTAGAGTG | 51317 |
rs147500718 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PHF21A | GRCh38.p7 | 11:46029857 | TATACAGTAAAAATA[A/G]TAACAAAGGCATAGA | 51317 |
rs147570145 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | PHF21A | GRCh38.p7 | 11:46105841 | AGAATTTTTGCTTCA[C/G]ATTCTGAATATCTTG | 51317 |
rs147604350 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | PHF21A | GRCh38.p7 | 11:45993886 | ACACCGACAGTGCCT[A/G]TCTGAGATGAATTTC | 51317 |
rs147638720 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46043909 | AAAACAGTAAAAGAT[A/G]GATCGCAGCAACTGC | 51317 |
rs147642157 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PHF21A | GRCh38.p7 | 11:46049219 | GTTCCCATCTCTAAG[A/G]GAAAGTAATACAGAA | 51317 |
rs147653802 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45939740 | CAGAATAAAGCAGAT[C/T]TACTTAAAATTGGAA | 51317 |
rs147745613 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | PHF21A | GRCh38.p7 | 11:46074753 | GGTGATCCACCCACC[C/T]TGGCCTCCCAAAGTG | 51317 |
rs147840395 | snp | C/T | 0.0678174 | 0.1712 | intron-variant | PHF21A | GRCh38.p7 | 11:46097469 | CTCCAAATATCTTCA[C/T]GGCTCACTCCCTCAA | 51317 |
rs147844953 | snp | A/C | 0.0221141 | 0.102801 | intron-variant | PHF21A | GRCh38.p7 | 11:45994993 | CACAGAAATGTGTAT[A/C]ATCTCTGTGCTATAT | 51317 |
rs147855084 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45999923 | TTGTCTTATCCTCTG[C/T]GCTAAGAGAAAGTCG | 51317 |
rs147855198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45942016 | GCCTCTCAAGTGTTA[C/T]TGTTTAATTAATGTT | 51317 |
rs147856081 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | PHF21A | GRCh38.p7 | 11:46104519 | TTTCTATTTTTCCCA[C/G]AGGTATTCACAAATA | 51317 |
rs147879950 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45958394 | ATGACAAAACCTGGT[C/T]TCAAAAAAAAAAAAA | 51317 |
rs147918963 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45972194 | GATCAGAAGATGAAC[C/T]GAGGTGAGAGGACTT | 51317 |
rs147954904 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:46019361 | CACTTGAGAACTAAT[C/G]CAGAAGCTAACTTTC | 51317 |
rs147958121 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46024706 | TCAGGAGGCTGAGGC[A/G/T]GGAGAATAGCTAGAA | 51317 |
rs147993479 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46079319 | CTTCTGTGATCCATG[C/T]AATAGGCTCAGGAGA | 51317 |
rs148023680 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | PHF21A | GRCh38.p7 | 11:45934901 | CATGCCATGGGTAGG[C/T]ATGGTGAGGAGGAGA | 51317 |
rs148103160 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46014422 | CACTGTTGATGGACA[C/G]CTAGGTTGATTCCAT | 51317 |
rs148136397 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:46093639 | TTCTTAACACTACTG[A/G]TATCTACAGGACTCT | 51317 |
rs148137663 | in-del | -/TC | | | intron-variant | PHF21A | GRCh38.p7 | 11:46010972 | AAAAAACTTTCTCTT[-/TC]TCTCTCTCTCTCACA | 51317 |
rs148155056 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PHF21A | GRCh38.p7 | 11:46116823 | CAAAACTTAGCCGGG[C/T]GTAGTGGCGGACACC | 51317 |
rs148163974 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46008999 | TTTTTTTTTTGGAGA[C/G/T]GGAGTCTCACTGTCG | 51317 |
rs148206958 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PHF21A | GRCh38.p7 | 11:46028786 | ACCATGTTGGTCAGG[C/T]TAGTTTCGAACTCCT | 51317 |
rs148225794 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46044461 | CTCCCCTTTCCACCC[C/T]CATTTGGATTTCATA | 51317 |
rs148263326 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | PHF21A | GRCh38.p7 | 11:45975038 | ATGGACTCAGGCTGG[A/G]CACAGTGGGTCATGC | 51317 |
rs148321076 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45968489 | ATTTCTCCACCCTGG[A/C]ACTACATACATGTTC | 51317 |
rs148380174 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PHF21A | GRCh38.p7 | 11:46040592 | GTTTAGCAACTAATA[C/T]AATCTAGTGCACCAA | 51317 |
rs148421329 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | PHF21A | GRCh38.p7 | 11:45970927 | TCCTTGGTGTCAGGA[C/T]GCTTCTGTAGTGATT | 51317 |
rs148421528 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46068942 | TGGCACGTTATTAAA[G/T]TATAAGTTACTCAAT | 51317 |
rs148431981 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:45973741 | CCTTGTTTTCCATTT[-/A]AAACATGTCGATTTA | 51317 |
rs148452083 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46005928 | CAGAACTCTCAAGAA[C/G]AGTAAGAAAAATAAA | 51317 |
rs148474957 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46063566 | CAAGCCATAGTTTTA[C/T]CAATCCCTGCCCTAC | 51317 |
rs148510705 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | PHF21A | GRCh38.p7 | 11:46083112 | TCACTCAGAAAAAGA[C/T]GAGCTTGTTTTTGTA | 51317 |
rs148516001 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PHF21A | GRCh38.p7 | 11:45980712 | TAACACAGATACTAG[C/T]CATAGTAATTTTTAT | 51317 |
rs148520597 | snp | A/G | 0.00130106 | 0.0254723 | intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45946039 | ACAAAAGGGAAAAAC[A/G]GGGAGGGAAAGAGAG | 51317 |
rs148536705 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | PHF21A | GRCh38.p7 | 11:45999099 | CCCAAAGTGCTGGGA[C/T]TACAGGCGTGAGCCA | 51317 |
rs148557580 | snp | A/G | 8.37402e-05 | 0.00647017 | missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934035 | GGGGAAGGGGCCGGC[A/G]TGGAGGTGGCGGCAT | 51317 |
rs148569754 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46073900 | ATCTCAAGTTACACT[A/T]TAAAAGCACTAGACC | 51317 |
rs148572056 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46035835 | AGAGAGAAAAGAGAG[C/G]TTGGAGAAAGTAGGT | 51317 |
rs148625216 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46017342 | GAAAAAATCAGATTT[C/G]TTTTTTTAGCACTCA | 51317 |
rs148678539 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PHF21A | GRCh38.p7 | 11:46011561 | TCTAAGATACTTTCT[C/T]GCTCTGGAAATCTAG | 51317 |
rs148683230 | snp | A/G | 0.108755 | 0.206276 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46119871 | AAAGAGTCCCACTCC[A/G]CGCGCCCCTCCCCCC | 51317 |
rs148692721 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45961093 | TCTGTTATACTCATG[A/T]TCCCACTGAAAGTGG | 51317 |
rs148713359 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | PHF21A | GRCh38.p7 | 11:46047617 | AAGCATAATTAAGAG[G/T]CTGAAAGATATTATT | 51317 |
rs148727925 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46031754 | AATAGTGTCTGGAAA[A/C]GAATGCAATAATTTT | 51317 |
rs148736290 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46111596 | CTGGAATAAGATACT[C/G]GCTAAGCAAGTAAGA | 51317 |
rs148783451 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | PHF21A | GRCh38.p7 | 11:45987446 | GTGGGCGAATCACAA[C/G]GTCAGGAGTTCGAGA | 51317 |
rs148787024 | in-del | -/ACAC | | | intron-variant | PHF21A | GRCh38.p7 | 11:46099523 | CTATAGAAAAATTAG[-/ACAC]ACACACACACACACA | 51317 |
rs148817669 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PHF21A | GRCh38.p7 | 11:46050085 | CCCAGCAGAGTTAGC[A/G]ATTGCCACTAGGGAT | 51317 |
rs148927461 | snp | A/G | 8.23662e-05 | 0.00641688 | synonymous-codon, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45971248 | CTGACTGTTGATGGC[A/G]GTCACCATAGCAATG | 51317 |
rs148943112 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45973408 | CTAGGGAGTTACTTA[A/T]CTCTATTTTTCTGCC | 51317 |
rs148964526 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46071314 | TAAACACATTTAGAG[C/T]AGACCTAACCAAACC | 51317 |
rs148975167 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46008714 | AGGAAAATAATAATA[A/T]ATGTTTTACATATCT | 51317 |
rs148998189 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PHF21A | GRCh38.p7 | 11:46065427 | AACAGCAGTGGTTGC[C/T]GACATGCTGAGCATG | 51317 |
rs149006078 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46096289 | AATTAAAAAAAAAAA[-/A]CCCTCTTGACTCCAT | 51317 |
rs149008108 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:45957752 | AACTAAATTCAAAGC[-/A]AAAAAAAAAAAAAAA | 51317 |
rs149031822 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PHF21A | GRCh38.p7 | 11:46001186 | ATCACAGAAGTCTAA[A/G]AAGAAAAACTTAAAG | 51317 |
rs149031990 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46106433 | GCTTTTTAGTATCAA[A/G]TCCTGATAAGTTAAC | 51317 |
rs149041324 | snp | A/C | 1.64735e-05 | 0.00286993 | intron-variant | PHF21A | GRCh38.p7 | 11:45949376 | ACTGGAACATGAGGG[A/C]AGGGCCAGATGCTGG | 51317 |
rs149085544 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46097255 | CTCTGCTCAAAACCC[A/T]CCAGTGGCTTCCCAT | 51317 |
rs149089014 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PHF21A | GRCh38.p7 | 11:46037598 | CGGTGAGCCGAGATC[A/G]TGCCAGCGCACTCCA | 51317 |
rs149191110 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46059492 | GTGCAGTGGTATGAT[A/C]ATAGCTCACTGTAAC | 51317 |
rs149246288 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:46034761 | CTGCAGAAACCAACA[C/T]GTCATATGTGTAAGA | 51317 |
rs149291896 | snp | A/C | | | downstream-variant-500B | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45929229 | ACCCCCCCGCCCCCC[A/C]CCCCCAGACAGCCAG | 51317 |
rs149312875 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:45977522 | ATGTAACAGGAAACA[A/G]TGAATTCTACCACAC | 51317 |
rs149348170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46054509 | TGATTCAACTGGTCT[A/G]AGGTGCAGCCCTGTA | 51317 |
rs149410030 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | PHF21A | GRCh38.p7 | 11:46093085 | TAGATTGTAAACCAC[A/C]TACACAAAAGCTATT | 51317 |
rs149457924 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46085117 | ACTCAAAATGGGGAA[A/G]TTCTGGTATAACTTA | 51317 |
rs149472218 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | PHF21A | GRCh38.p7 | 11:45937766 | GATTACAGGCCTGAG[C/T]CACCACGCCTGGCCC | 51317 |
rs149491141 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46073612 | GACACTGTTTTTGCA[C/T]ACGTTTACACGCCCA | 51317 |
rs149508155 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46011416 | ATCGCCTGAGCCCAG[C/T]AGGTGGAGGTTGCAG | 51317 |
rs149526820 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46028369 | GTGTTAAGCTTACAG[A/G]CAATTCTCACTTTGC | 51317 |
rs149544562 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PHF21A | GRCh38.p7 | 11:46068443 | GTGGTGTCAGTTATA[C/T]TGGCTCCTAAAAAGC | 51317 |
rs149552621 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46111117 | ATCACAACTATGTGG[C/G]GGGGGAGGCTAGTAT | 51317 |
rs149561785 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | PHF21A | GRCh38.p7 | 11:45968167 | TTATTACCATTATTG[A/G]CAATGTCTTAACTGT | 51317 |
rs149567292 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45954006 | TTTTTTGTTGTTGTT[G/T]TTGTTTTGAGATGGA | 51317 |
rs149588947 | snp | C/T | 3.34829e-05 | 0.00409149 | synonymous-codon, missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934223 | CTTCATTTCCATGCA[C/T]TTCTGCAGCAAATGA | 51317 |
rs149612103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46100777 | GTCTACCATTACCTT[A/G]TAGTGACTCCTAATG | 51317 |
rs149615090 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46040277 | AAAAGAGAGGAAGGA[C/T]GGAGGCAGGGTGGGG | 51317 |
rs149618563 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PHF21A | GRCh38.p7 | 11:45945215 | TGCTCAGCAGAGTAG[C/T]GCTCAGTGAGTATCT | 51317 |
rs149654239 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | PHF21A | GRCh38.p7 | 11:46113694 | AGTTGGGCGTGGTGG[C/T]GCACGCCTGTAGTCC | 51317 |
rs149661811 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | PHF21A | GRCh38.p7 | 11:45970260 | CTGCTTAGCCAAATA[G/T]GCTTTTTCCTGATAT | 51317 |
rs149670458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | PHF21A | GRCh38.p7 | 11:46049488 | ACTGGTAGAGGGAAA[C/T]AGATGGCTTCTAAAA | 51317 |
rs149701129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46023303 | GCTAATTACTGAGGC[C/T]CCTTCTATTTTGAAC | 51317 |
rs149723916 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PHF21A | GRCh38.p7 | 11:46043584 | CTGCCAAACTGTTCT[C/T]CATCTCTAAGGCAGT | 51317 |
rs149810589 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | PHF21A | GRCh38.p7 | 11:45988387 | TAGCAGGCAGTATAT[A/G]TCATGTAGAAAATAT | 51317 |
rs149812378 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46065376 | TGTTGATGTGTGAAG[A/G]TGTAAAGCCTGGCAC | 51317 |
rs149863118 | snp | C/T | 0.00111971 | 0.0236347 | intron-variant | PHF21A | GRCh38.p7 | 11:45979757 | TTCCATCCACACATT[C/T]ACCTGTGAAGCAGTC | 51317 |
rs149866605 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46057430 | TATAACAGATGCCCA[C/G]AGCATTAGGGCTTAA | 51317 |
rs149880029 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46000429 | ATGACCATTAGCTGC[A/G]ATATGGGACTAAAGA | 51317 |
rs149898933 | snp | A/G/T | 0.000386905 | 0.0139035 | missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45933999 | CCCTGGTTACAGTTC[A/G/T]CTGTGCAGCTCTGGG | 51317 |
rs149901976 | in-del | -/AGCTTTA | 0.206336 | 0.246157 | intron-variant | PHF21A | GRCh38.p7 | 11:46000499 | TGAATAATTTTAAAC[-/AGCTTTA]AGCTTTAAAGACTCT | 51317 |
rs149931947 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PHF21A | GRCh38.p7 | 11:45993601 | TCACAGGAGGTTGGG[C/T]GGCATCCAAGCAGAC | 51317 |
rs149934794 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | PHF21A | GRCh38.p7 | 11:46096952 | AAATGGTAACTCCAC[A/C]CCCTCAGAAGAAAAA | 51317 |
rs149963060 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45987658 | AGAGCAAGACCCCGT[C/T]TCAAAAAAAAAAAAA | 51317 |
rs149987752 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PHF21A | GRCh38.p7 | 11:46088815 | TAGGCTTTTCTGTTC[C/T]CAAATTCTCTAAGGA | 51317 |
rs150020599 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PHF21A | GRCh38.p7 | 11:45941444 | CATCATCACACATCA[C/T]GCAATATCTGGTAAA | 51317 |
rs150029824 | in-del | -/AT | 0.20511 | 0.245937 | intron-variant | PHF21A | GRCh38.p7 | 11:46024014 | GTAGCAACCTGTAAC[-/AT]GTGGGAACACTGATG | 51317 |
rs150071758 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PHF21A | GRCh38.p7 | 11:45933366 | CTTGCACGAGGCCCC[C/T]GCCAGAGGTGATTAA | 51317 |
rs150108211 | snp | C/G/T | 0.00557861 | 0.0525638 | intron-variant | PHF21A | GRCh38.p7 | 11:46100120 | AACATGCCTCAATCA[C/G/T]GCTGATAAGTAAGTA | 51317 |
rs150111211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45997114 | TCTGAAAGTGTTTGG[C/T]GGAGAAATGTTTGTT | 51317 |
rs150120810 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45944535 | GCCCTGCGCAACTGG[C/T]CCAGCCACTTCTGAG | 51317 |
rs150131940 | in-del | -/CACACACACACACG | | | intron-variant | PHF21A | GRCh38.p7 | 11:46040922 | ACACACACACACACA[-/CACACACACACACG]CACGCACAATTAAGG | 51317 |
rs150161686 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46091087 | AGGATTAACTAGTTC[A/C]AGTGCCTCCATTAAA | 51317 |
rs150178295 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | PHF21A | GRCh38.p7 | 11:46033566 | ACCATGCTTAGCCCA[C/T]TTTCTGTTATTATTA | 51317 |
rs150179334 | snp | A/G | 9.7028e-05 | 0.00696452 | intron-variant | PHF21A | GRCh38.p7 | 11:45935539 | TAAACAGAAGGACCC[A/G]AAACAGCCTGGGGCC | 51317 |
rs150184344 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | PHF21A | GRCh38.p7 | 11:46117472 | CTCAGTCTTTGCAGG[C/T]TAACTTAAGTACATC | 51317 |
rs150213753 | in-del | -/AAGGCCA | 0.021333 | 0.101051 | intron-variant | PHF21A | GRCh38.p7 | 11:46012769 | AAATCTGGCCTGCTT[-/AAGGCCA]AACTCATTGTCTTCC | 51317 |
rs150224569 | snp | A/G | 8.24002e-05 | 0.0064182 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45979955 | CTTCCGTAGCTGTTC[A/G]ACTACTCTTTTCTAC | 51317 |
rs150231324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46026537 | GAAAGCTTTAGCTAC[C/T]TCTTCTCTACCCTGT | 51317 |
rs150235608 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | PHF21A | GRCh38.p7 | 11:45966041 | ACTCCTCCTCTCAGT[C/G]TCCTTTGTGGGCTTA | 51317 |
rs150265682 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46053275 | AATATCAATATGAAA[G/T]AATTATTAGTGAAAC | 51317 |
rs150297594 | in-del | -/A | 0.0146672 | 0.084371 | intron-variant | PHF21A | GRCh38.p7 | 11:45970024 | ACAAGCTTTCATCGT[-/A]AGTTAATCATCTGAA | 51317 |
rs150319005 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46045725 | ATCTGTTCTCTAAAA[C/T]ACGTAGGTTACTAGA | 51317 |
rs150331614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45990601 | CTAAGTACTGAAGCT[A/G]TGATTCATGCTTTTA | 51317 |
rs150340926 | snp | A/G | 0.00438332 | 0.0466095 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45929659 | TGGGGAAGGGGTAGG[A/G]GGGTGGGGTCCTCAG | 51317 |
rs150383513 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:45983484 | GTTATACATGTCTGT[C/T]GCTATCTGTGAAAAA | 51317 |
rs150386291 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46084941 | CATCTCAGCCTCCCA[A/G]AGTGCTGGGATTACA | 51317 |
rs150395204 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46060870 | CTTTTGCACCTTCAT[C/G/T]GTGAAATCTGTGCCC | 51317 |
rs150425973 | snp | A/T | 0.000115412 | 0.00759556 | missense, synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934176 | TTCTCCAGGGAGCTG[A/T]GCATCTCCTTCTGCC | 51317 |
rs150440208 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PHF21A | GRCh38.p7 | 11:46076339 | AACCTACATTTAGAG[C/T]AATCTACTTACAAGA | 51317 |
rs150457423 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | PHF21A | GRCh38.p7 | 11:45962556 | AGGCTGCCCAGCAAA[C/T]TAAAATAACAATGAC | 51317 |
rs150501546 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PHF21A | GRCh38.p7 | 11:46022971 | GGCCAGGCTGGTCTC[A/G]AACTCCTGATCTCAG | 51317 |
rs150537895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46079733 | GGAAGTGCAGGAACA[A/G]TACAAAACTCTATCT | 51317 |
rs150586830 | in-del | -/A | 0.0263992 | 0.111815 | intron-variant | PHF21A | GRCh38.p7 | 11:45991960 | ATGATTACATTTTGC[-/A]AGACATGTAATAGGA | 51317 |
rs150618234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45959647 | AAAAAACTCAAAGAA[C/T]CCATAAAACAAATAC | 51317 |
rs150639079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46103636 | TGGGTTAGTGAGAAC[A/G]AAAAGTTAATAGGAG | 51317 |
rs150642561 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46042871 | TGCTGATGCCTTGAA[C/T]GTGGACATCCCAGCC | 51317 |
rs150695006 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46036066 | TAATGGCATGGGCTA[A/C]AGTAGTGCTTATGGA | 51317 |
rs150702606 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45975367 | TAAAATAAAATAAAA[C/T]AAAATAAAATAAAAC | 51317 |
rs150727247 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PHF21A, LOC105376661 | GRCh38.p7 | 11:46122970 | ATAGTGTTGGCCTTC[G/T]AATGTTAAATAACAA | 51317 |
rs150763047 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:46067762 | TTCTAGACTTGAGGG[C/G]TACAAATGTGAGCAA | 51317 |
rs150791694 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46074455 | ATAAGTGGCTCTTTT[-/G]GGCGGGAGGGGGGAA | 51317 |
rs150848173 | in-del | -/ATCT | 0.272693 | 0.248968 | intron-variant | PHF21A | GRCh38.p7 | 11:46015896 | TGCTGTTTTACAGTC[-/ATCT]ATCTATCTATCTATC | 51317 |
rs150871012 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45932722 | TAATTTAAAAAAAAG[C/T]TTTTTTTCCCCAGAT | 51317 |
rs150902436 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | PHF21A | GRCh38.p7 | 11:46003202 | AAGAAAATCTGTATA[A/T]GAGAGTGCCACTAAA | 51317 |
rs150905645 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46088240 | ACCATCAGACTCACA[A/G]GACAGTAACACACTG | 51317 |
rs150954424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46050347 | AGTGGCCGGCTTACT[C/T]TGATCAACTGAGTGG | 51317 |
rs150956438 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PHF21A | GRCh38.p7 | 11:46012152 | CTGCCTGAAGTTCAT[A/G]CCATCTTTACCCTAA | 51317 |
rs151009796 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46006787 | CAATAAAAATGGCAC[A/T]AAAATATTTTAAGAC | 51317 |
rs151015262 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:46090539 | AGATTCACAATGCAC[A/C]TTAGCATATTAAAGG | 51317 |
rs151015910 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | PHF21A | GRCh38.p7 | 11:45989796 | TTGGGCCCAGGAGTT[C/T]GAGACCAGCCTGGGC | 51317 |
rs151038480 | snp | C/T | 1.64841e-05 | 0.00287085 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45979829 | GTGGTACTGCTGCTG[C/T]TGTTGTAGTTGCTGT | 51317 |
rs151045696 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46025862 | GGTGATGGGCTGTGA[C/T]TGCTCATAGCCCATT | 51317 |
rs151069410 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PHF21A | GRCh38.p7 | 11:46083384 | AGATATTCTCCCAAC[A/G]ATTTCAAAAGTTAAT | 51317 |
rs151072512 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:45946169 | AGGAAGGAAGAGAAG[C/T]AAAGATTTAAATGTC | 51317 |
rs151078594 | in-del | -/ACAC | | | intron-variant | PHF21A | GRCh38.p7 | 11:46099524 | CTATAGAAAAATTAG[-/ACAC]ACACACACACACACA | 51317 |
rs151079931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46018413 | CAGTATAGTATTAAC[A/G]CTTAGCCTCTGGTGT | 51317 |
rs151090965 | snp | C/G/T | 0.000182869 | 0.00956065 | missense, utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934057 | TGGCGGCATTGGCAG[C/G/T]GGGGGTGCAGTCCGG | 51317 |
rs151158619 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | PHF21A | GRCh38.p7 | 11:46107528 | CTGCTACATTCTACC[A/G]GGTCCAATTCTTAGA | 51317 |
rs151169176 | snp | A/T | 0.0137019 | 0.0816284 | synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45965540 | CTGGATAAGCTGAGG[A/T]GCTGCGAGCATGGGA | 51317 |
rs151205906 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:45982921 | ACTATACCAGTCACA[A/G]AAGGAAAGGGTGTTT | 51317 |
rs151220439 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46056602 | AAGAAATCTAAACTC[A/G]TTCAAGATAGACAAT | 51317 |
rs151221058 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:45961438 | CCAGTATTAAAATGG[A/G]GTAAGGGGAGGCATC | 51317 |
rs151228359 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | PHF21A | GRCh38.p7 | 11:46038363 | GAACTCCTGACCTCA[A/T]GTGATCCACCCGCCT | 51317 |
rs151237777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45976223 | GCTCTTTCCCCTTTG[C/T]TCTATCACTAAAATC | 51317 |
rs151253135 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45940345 | GGATTACAGGCGCCC[A/C]CCACCACGCCTGACT | 51317 |
rs151256197 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46075978 | TTTTGATTAATATAT[G/T]CACCTACTCCAAGAC | 51317 |
rs151279777 | in-del | -/TCT | | | cds-indel, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930972 | TGGGTGCCAGGGGCC[-/TCT]TCTTTACAGTAAAGC | 51317 |
rs151309055 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46069770 | ATCTCAGTTTATGTA[G/T]CACAATGATGCACTT | 51317 |
rs180739118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45948276 | CTGCTCTGCCTAAGA[A/G]TAAGATTCTGGAATG | 51317 |
rs180743572 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45974253 | TTAGATCTTTACCCC[C/T]ACTCTGGTGCTTCTT | 51317 |
rs180750369 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46007841 | TTTCAAATTTTAGAA[C/T]AAGGGACTTTTCCAT | 51317 |
rs180753063 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45996929 | GCACAAATGTATCCA[C/T]TGTAAATGTTAGTCT | 51317 |
rs180788005 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | PHF21A | GRCh38.p7 | 11:46015392 | TACAATTACTTTTGA[A/G]GACTTAGCCATAAAT | 51317 |
rs180797007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46038137 | CTCTCTCTTTTTTTT[C/T]TTAAATGGAGTTTTG | 51317 |
rs180886193 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46116413 | CTTGAACCATGACAT[A/C]TGTTACTCTGTCAAT | 51317 |
rs180909664 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46092636 | TCCTCATAAAAGGCA[C/T]TTTTTTCAATTAATC | 51317 |
rs180913920 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46069860 | AGATGAAAGTGTTAC[A/G]TATGAGATGAAGTTA | 51317 |
rs180922435 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46048997 | CAGAAGGGAGACTAT[G/T]AACTAGCTGTCTGTT | 51317 |
rs180928629 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46027337 | GTTTACCTTATTTAT[A/G]CATGTATAAGGGGTT | 51317 |
rs180944051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46103893 | ATAGAGACATTCGTA[A/G]GACAGATACATATAT | 51317 |
rs180962152 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46058012 | TGCAAACGTTTTTCC[A/G]TCAGTTAAGTTTCCA | 51317 |
rs180993881 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46080528 | ATGATTATATTAATA[C/T]ACTAAACTATAAACA | 51317 |
rs181036905 | snp | C/T | | | upstream-variant-2KB | PHF21A, LOC105376661 | GRCh38.p7 | 11:46123405 | ATGGACTTTATGGTA[C/T]ATGTGTAGGCCATTT | 51317 |
rs181043186 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:46097499 | AATTATTGAGGAAAT[C/T]TACAGCAGTTTCAGG | 51317 |
rs181045463 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:46073253 | GAATGGCGTGAACCC[A/G]GGAGGCGGAGCTTGC | 51317 |
rs181049397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46053183 | TGATAAATGTTTGGT[C/T]TCACAGAACACTAGA | 51317 |
rs181056169 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46030498 | AGATCCAAAAAGAGA[C/T]AACAAGGAAAGTATT | 51317 |
rs181091821 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46063495 | AAATGTAAAGAGTGT[C/G]ATTGTGTTCTAATAA | 51317 |
rs181153964 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:46011045 | CATCTGCTTAATTAT[A/G]GTTCCCTTTCCCCTT | 51317 |
rs181175786 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45929142 | GGCACTCTGGGGCTA[A/G]GGCGTCAGTGCACAA | 51317 |
rs181182379 | snp | G/T | | | upstream-variant-2KB | PHF21A, LOC105376661 | GRCh38.p7 | 11:46123021 | ATACAAATGGGGGGG[G/T]GGGGGGTTTTGTTTT | 51317 |
rs181189621 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46069519 | AGGCTGGAGATAGTC[A/T]TATATCAGGTAACCA | 51317 |
rs181205426 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45960780 | TGGTCTCTGAGATTA[G/T]AAACCATGATGCAGA | 51317 |
rs181210071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45987857 | CATGGCTGTATCCCA[C/T]AACCTAAAGGCAGCA | 51317 |
rs181218749 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46007630 | CCATCTATCTTTTAT[G/T]ATAGTTTTACTGTTA | 51317 |
rs181222709 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45967884 | AAACTTTCTGAAATA[C/G]AGAACACAGTATGTG | 51317 |
rs181232204 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45943222 | CAGCCTCCCATGCTC[A/C]AGTGATCCTCCCACC | 51317 |
rs181243894 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PHF21A | GRCh38.p7 | 11:45991653 | GCTGTAAAAATAATA[C/T]ACTGGGTCGAGAAAC | 51317 |
rs181273566 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46087954 | TAGTGACAGGGTTTC[A/G]CCATGTTGCCTAGGC | 51317 |
rs181360844 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45937485 | GTTGTTTTATTATTA[G/T]TATTATTTTTTTGAG | 51317 |
rs181363705 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46111114 | TAAATCACAACTATG[C/T]GGGGGGGGAGGCTAG | 51317 |
rs181405555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45941819 | TGTTTTTAGGAAGCA[C/T]TCTGGCAATACCAAC | 51317 |
rs181406324 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46115759 | AGAGACCTAAAACTT[C/T]AATTCCTTCCCTTCT | 51317 |
rs181409485 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45967613 | TTACACCTGAGCTAT[A/C]CTTGGACAGCTGTAG | 51317 |
rs181418608 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46048934 | TGGCTGTAACATTTT[A/T]CATTCCCACCAGCAA | 51317 |
rs181419763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45991208 | GTTTTTCATGGTTTG[A/G]TAGTTCATTTCTTTT | 51317 |
rs181424532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46068832 | CTTACAAGAGGATTG[C/T]TCTGCCTTAACTCAG | 51317 |
rs181429800 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46010803 | CCCTGACTAACTCTA[C/T]ACCCCTACCCAGTGG | 51317 |
rs181439770 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46026862 | AAGGCCTTACATCTT[C/T]AAATGCCTGGCCCAC | 51317 |
rs181443157 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45947050 | CATCCTGATAAACTA[C/T]ATCTCTAAAAATTGG | 51317 |
rs181465065 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | PHF21A | GRCh38.p7 | 11:45995670 | AAGGCTCTACAGAGT[C/G]TGCAAGACCAGCACA | 51317 |
rs181470648 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46030380 | TATTCTTACCAAATG[A/C]TTTGCCCAGGTTTTC | 51317 |
rs181516764 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930827 | GTGGGGAAAGAGCAG[C/T]GGAGGGAAGGAGGAG | 51317 |
rs181536064 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45981279 | TAATCCCAGCTACTC[A/G]GCAGGCTGAGGCAGG | 51317 |
rs181557749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46092438 | AAATTGCTACTTTTC[C/T]ATAGTTTTTCAAGAC | 51317 |
rs181566461 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46048422 | TCCATCAGTTTATGG[G/T]TTGTTTCCACTTTTT | 51317 |
rs181591588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45973971 | TCTACAAAATACTGA[C/T]TAAAGCCTCAAACTC | 51317 |
rs181620004 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46017578 | AGGATTTGCCCTTAA[A/G]GGGGAAAAAAAAAAA | 51317 |
rs181627396 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46022226 | GGGAGGCCAAGGTGG[C/G]AGGACCACTTGAGAT | 51317 |
rs181646403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46052638 | AGAAGAAAGATATTC[A/G]TGAAGCTAAATTGCT | 51317 |
rs181660086 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PHF21A | GRCh38.p7 | 11:46109850 | CCGGGTGTGGTGGCA[C/T]ATGCCTGTAGTCCCA | 51317 |
rs181663065 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46087506 | AAGTTAGGACTAGTT[C/G]TAGAAAAACATATGA | 51317 |
rs181666044 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46062795 | AAACACACCTACTAT[A/G]CAACCCAGACATACT | 51317 |
rs181670164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45953231 | AGCTGGGAAAATCAT[C/T]GCTCATCTTAACATT | 51317 |
rs181698168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46002776 | CCTCAAACCCCTCCA[C/T]AGAACTAGTTTTATC | 51317 |
rs181715489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46072881 | TTCGGAATGTTAAGA[C/T]TGCCTCTACAAGAAA | 51317 |
rs181775441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46059161 | AGGAAATAATCAAAA[C/T]TACGTACAAATATTT | 51317 |
rs181777392 | snp | C/T | 6.81733e-05 | 0.00583798 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45935734 | TCTGTTTCTCTTCTT[C/T]TTTTGCTAAAAAAAA | 51317 |
rs181778635 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46092082 | CCCATTTCTGAGAGA[C/G]AGCCTATTTGCCAAA | 51317 |
rs181780211 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:46115215 | CAAGTCTAGTGTAAG[A/G]AAGTTGCTTTAGAAG | 51317 |
rs181783081 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46039105 | GGGGTCTGACAGACA[A/C]CTCTAAAGACTTGAC | 51317 |
rs181798529 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46015545 | TTGCTTTATAAAGTT[G/T]AATTTTTAAACTTTT | 51317 |
rs181798557 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46068354 | AAAAGGGAATAAATG[C/G]GAATGGATTTTTTGA | 51317 |
rs181820915 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45968958 | AAAAAAAAAAAAAAA[A/T]AGGCAGGTATCCCTC | 51317 |
rs181882731 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PHF21A | GRCh38.p7 | 11:45948653 | CTACATTAAGCCATT[C/T]CCCTGAGTCAGCTTT | 51317 |
rs181888920 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | PHF21A | GRCh38.p7 | 11:45975319 | ACCCTGTCTCAAAGA[A/C]AACAAAATAAAATAA | 51317 |
rs181892368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45998044 | ATCAGTAGCAATCAG[C/T]CTGCTACCCAGGAAT | 51317 |
rs181923782 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46081314 | AACAATACATATTCC[A/G]AGAGTTTAAAGGGGA | 51317 |
rs181924410 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45943451 | TCCCAAAGTGTTGGG[A/T]TTTACAGGCGTGAGC | 51317 |
rs181928955 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46001508 | TCTCCGTCACATGCA[A/C]CACAGCATCAACAGA | 51317 |
rs181949950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46047397 | CTGGTAAGGTATTTT[A/G]TAATTTTTTTTTATT | 51317 |
rs182016257 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45959177 | GGTATCTCAACTGGT[A/G]TAGAAAAAGCATTTG | 51317 |
rs182020662 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46099556 | CACACACACACACAC[A/C]CACACACCCTAAACA | 51317 |
rs182037599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46007134 | CAACCATAACGTGAC[A/G]AGACATCTATCAACA | 51317 |
rs182047502 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46063832 | TACTGTTTCATCTGA[C/T]GAACCCACATCATAG | 51317 |
rs182051392 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45936915 | ATCAGCATGATGGCA[C/G]CAGCCACTGGCAGTT | 51317 |
rs182052056 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46086725 | TTTGAAGTTGAAGGT[G/T]TATTTTTCAAATATT | 51317 |
rs182054401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46062522 | CCTCTCCTTGTTTCA[C/T]TAATGCAATATCTTC | 51317 |
rs182062674 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46043247 | CCTATCAATGATCCT[A/G]TTCTATCCAAGGACT | 51317 |
rs182073647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46043608 | AGGCAGTATTAACAC[A/G]TTACAAAGTGCCAAA | 51317 |
rs182077352 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46019930 | ATAATCTTAATCATC[A/C]TGTCATCTCATTTCA | 51317 |
rs182085508 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45952588 | TAGTACTTCTTTTTG[G/T]CTTAAGTTTTGGTCC | 51317 |
rs182090821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45980302 | AAAAGCAGGACTCTG[A/G]AGCCATCCTACTTCA | 51317 |
rs182103079 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45944029 | AAAATAAAGGATTAC[A/C]AAACAGACAATATCA | 51317 |
rs182113813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45988233 | ATATAACAGATTATT[C/T]AACCAAATTCTATGC | 51317 |
rs182115466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45949926 | ATCAGAAGAGCACTT[C/T]GCTGTGCTGTTCAGA | 51317 |
rs182148362 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45992299 | GCACTTTGGGAGGCT[A/G]AGGCGGGCAGATCAT | 51317 |
rs182201285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46104371 | TACTATAAACTGCAT[C/T]AATATCTTGGTGCTG | 51317 |
rs182235745 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46025777 | TCTCTGGAATTATTT[A/G]CAAGTCATAGGCATA | 51317 |
rs182253464 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46073723 | GAGCACATTCCTGTA[A/T]CATTAAAATACTTTC | 51317 |
rs182258111 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PHF21A | GRCh38.p7 | 11:46108751 | TAACACTCTAAAACG[C/T]TGATCGTTATATAAG | 51317 |
rs182289031 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:45976215 | CTTGTGAAGCTCTTT[C/T]CCCTTTGCTCTATCA | 51317 |
rs182293776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46031072 | TACGACAAGCGATCA[C/T]GTAGTAAAAGCTGTG | 51317 |
rs182299431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45935607 | TCTGCACCTATGTAT[C/T]GACTGCTGAAGGCAT | 51317 |
rs182317494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45987310 | TCAAAGACCCTAGAC[A/G]CAGTAAATACCTAAG | 51317 |
rs182318788 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46118476 | AGCCAGATGTTTGTG[C/T]TTTGAGAACTTTGTG | 51317 |
rs182407404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45970153 | AACATAGCAGGCTCA[A/G]TAAATCTTAGACAAT | 51317 |
rs182421231 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46049562 | GCGGGGGAAGGAGGG[A/G]TAGAAAGAGGATAGG | 51317 |
rs182440893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45938050 | ATGCAGCCCGGAGAC[A/G]GACTGGGAGAGAGAA | 51317 |
rs182477810 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45932069 | CAGAGCGAAGGCCAC[A/G]CTGGGGCTCTGTCTC | 51317 |
rs182485583 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45954348 | AACCTGCTTAAGATC[A/C]GAATGATGTTAAAAA | 51317 |
rs182490297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45982618 | CATGTAAATTTTATT[A/G]CTTGGTGACTGCTAG | 51317 |
rs182499847 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46003572 | ATGATGACATTTTCA[A/C]GAAGGGCAGAGTGAG | 51317 |
rs182523856 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | PHF21A | GRCh38.p7 | 11:46098342 | CTATATGCTTGAAAA[A/C]TGTGAGCCACACTAG | 51317 |
rs182525415 | snp | G/T | | | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45965353 | TAAGCTGTACAGTTT[G/T]AGGTCCAGCGAGTCT | 51317 |
rs182551157 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:46053713 | CCTCATCTTCCTCCC[A/G]TTCTTCTTCCTGGTT | 51317 |
rs182568631 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46012107 | CTGTTCATTACTACC[A/G]GAAAGAATCCTTCAA | 51317 |
rs182590564 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45929541 | CTCTTCTCTGCTAGG[A/G]GCTGGCTGACCTCTG | 51317 |
rs182613060 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45931276 | GAAAAGGTAAGTTAG[A/G]TGTTGTGTGGCAACC | 51317 |
rs182614957 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46105477 | TTCTCCACACTCAGA[A/C]CCACACTAACCAGGA | 51317 |
rs182632943 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:46059555 | CTCAGCTTCCCAAGT[A/G]GCTGGGACTACACAC | 51317 |
rs182644733 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46016672 | CTGCAATTTGTAGCT[C/T]ATGTTTTTCTCCTCT | 51317 |
rs182656431 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46100265 | GGCTTCCATTAACCT[C/T]GTTTAAAAAAAAAAA | 51317 |
rs182668205 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46075346 | CACTAATCAGTTCTC[A/T]CCTTCTTCCCCTGCT | 51317 |
rs182674816 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46055128 | TTTTAAATTATGGCG[A/G]GAACTTAAGATACTT | 51317 |
rs182677662 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46032304 | CCCAGAAATAAGCTC[C/T]GTTATTTCTTTCTAA | 51317 |
rs182702365 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:45963551 | TTACGGGGAAAAGCA[C/T]CTTCTACAATTTATA | 51317 |
rs182704551 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46100874 | ATAGCAAGTTTCTAA[A/C]CACTGTTACCACGTC | 51317 |
rs182709968 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45939826 | TCTTTTCCAGAGAGT[C/G]AATGCCTAGCTCATT | 51317 |
rs182714947 | snp | C/T | 0.00208187 | 0.0321963 | intron-variant | PHF21A | GRCh38.p7 | 11:45965301 | CCCAGAGCAGGTACA[C/T]ACTCTGCCTGTACCT | 51317 |
rs182722540 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45988924 | TCTAAAGCTGCTGAA[G/T]GCTACCCTCTTAGTT | 51317 |
rs182727342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46009490 | CATCTAAACATGTAA[C/T]GATAATAGCAGCTGC | 51317 |
rs182780921 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46013315 | TCTCTCCCTGTCCCA[C/T]CCCTTCCTACCCAGA | 51317 |
rs182786102 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46043798 | TGTCATATACCCACA[C/T]TGAAATGAATGCTCA | 51317 |
rs182788459 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46104700 | AGAGCAGCTATCATG[A/G]TTGAGTGTCTCAAGA | 51317 |
rs182790040 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46082758 | TGGTATGCTTGAATT[A/C]AGAATATGAAACAAA | 51317 |
rs182794799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46028723 | GGATTACAGGCGCCC[A/G]CCACCACGCCCAGCT | 51317 |
rs182802176 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46059240 | TGGGAATAATTTAAA[C/T]GTCTAAAAATAGTGA | 51317 |
rs182807079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46039456 | GGAAGCCTGAGAATA[A/G]TCAGGTAAGTACAGG | 51317 |
rs182874361 | snp | A/G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46049856 | TTCCTAAAAACAACG[A/G/T]TAAGACTATCCAGCA | 51317 |
rs182894062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46083985 | AGTCAGGAATACTTT[A/G]AGTTCTTAAAAGCAG | 51317 |
rs182913622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46112133 | TAGTCAAAATATTCA[A/G]TTACTGGTGTGATAG | 51317 |
rs182914470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46040485 | GTGGGGAGGGGTGAC[A/G]GCTTGGGGCTCTGTA | 51317 |
rs182922109 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PHF21A | GRCh38.p7 | 11:46089232 | TTTACTTCTTGTACC[A/G]TGCTTAATATTTGAA | 51317 |
rs182930796 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45944772 | ATCCATTCCATTTTT[G/T]ATCTCTTTTTAGAGA | 51317 |
rs182942592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45970839 | AAATGAAACAGTGTG[C/T]ATGCCTCTGTGAAGG | 51317 |
rs182962836 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PHF21A | GRCh38.p7 | 11:45998984 | GGCACCTGCCACCAC[A/G]CCTGGCTAATTTTTA | 51317 |
rs182969112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45972058 | CCAGTTCTTGATACT[A/G]AAGGGATATTATGAG | 51317 |
rs183018182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45949323 | GCTGCTCTTCAGCAG[A/G]TTTTCAGAGGGGAGG | 51317 |
rs183041770 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | PHF21A | GRCh38.p7 | 11:45998403 | AATATGCCTACTGAG[A/T]ATATAGTATTGTAAC | 51317 |
rs183086827 | snp | A/G | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46022766 | TGATCCACTGTGCCC[A/G]GCTCATATACTGTTA | 51317 |
rs183093713 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | PHF21A | GRCh38.p7 | 11:46054198 | AAGAATTTCAACCAA[C/T]TCATTTAAAAAAATT | 51317 |
rs183101819 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46032104 | CTCAAAAGGAGACAC[A/T]CCAGAGTTTGATTTA | 51317 |
rs183110833 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46012933 | TCCTGCTGCTGTACT[A/T]CAGTCCTCATAGGGG | 51317 |
rs183122641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46070772 | ATTTAAAACCAAAAG[A/G]TAATTTATGGAATAC | 51317 |
rs183123522 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45992701 | ACAAAAGGCAAGTTA[C/T]ATGAATGAGTTCTGA | 51317 |
rs183172597 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45974927 | AAATACATGGCATGG[A/C]AAATACTGCCAATAG | 51317 |
rs183198309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46106666 | TACAACCACTTGTAC[C/T]TAACATGCATGCTGC | 51317 |
rs183213772 | snp | A/G | 0.0146672 | 0.084371 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46084374 | TGTTAAATAAATTAT[A/G]TTAGTAAAAGAATAT | 51317 |
rs183214589 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46060731 | TAGACCTTTGTCAGA[G/T]GCACAGTTTGCAAAC | 51317 |
rs183221783 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46117244 | TTTCTAGCATCCCCA[A/T]ATTTTTAAAACTTCG | 51317 |
rs183225167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46041518 | TTCATCTTGGTTTCA[A/G]TTATAGCCAGGCCAA | 51317 |
rs183232442 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45999232 | GAAAACAGGACCACA[A/C]ACAGAGGTCAAGATC | 51317 |
rs183240919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45946452 | GCTGTGGCACGATCT[C/T]GGCTCACTGCAACCT | 51317 |
rs183259824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45994042 | AGGGCAGCTGAGCAG[A/G]GATAAATGCTGGAGC | 51317 |
rs183277474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45983954 | TGTTTTAAATGAAGA[C/T]GTCATGACTGCTGCT | 51317 |
rs183281727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46003947 | TTTGGAAATACATCT[C/T]TATGAAAATATGTAT | 51317 |
rs183296617 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45976060 | AACCCAGAAGCTCTG[A/G]CATGCTTTGGAGGGC | 51317 |
rs183320866 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46117396 | ATATTCATCTTTATG[A/C]AGTTACTGTTACATC | 51317 |
rs183370084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46094363 | TAGAAAATCAAACCC[A/G]GAAAAGTTAAGTGAT | 51317 |
rs183374064 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46111305 | TGAAACCCCATCTCT[A/G]CTAAAAATATAACAA | 51317 |
rs183386217 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46088829 | CTCAAATTCTCTAAG[G/T]AGGTTCTTCTAACTA | 51317 |
rs183393208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46050283 | AGTGTCCTTGCTCAC[A/G]GCAGGAGAAAGGCAT | 51317 |
rs183397907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46064556 | ATTTTGCAGGACAGC[C/T]TCCCATCTAACCAGC | 51317 |
rs183402691 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46044239 | TGTCCTATAGTACAG[C/G]TAGAGGTACCTTTTG | 51317 |
rs183411100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46023663 | ATGTGTGTTAAGAAT[C/T]ACTGAATGGAGGCCA | 51317 |
rs183424234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46015844 | GGTAACAATGCCTTC[A/G]TCTGAAATACCTCCT | 51317 |
rs183485406 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46064742 | TATTAATATCAACAA[C/T]GATAATGATAGTTTA | 51317 |
rs183488551 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46099720 | ATCCACATTTCAAGC[A/G]CTAAAAGAATTAACA | 51317 |
rs183497945 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46023854 | CCAGCTACTCAGGAG[C/G]CTAAGGCAGGAAAAT | 51317 |
rs183541088 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45933815 | AATTGGCAAACTCTG[A/G]TGCCACCTGGCACAA | 51317 |
rs183558667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45984383 | GATTCCCTTGACATT[C/T]GCATCACTGGGTTTC | 51317 |
rs183640689 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PHF21A | GRCh38.p7 | 11:46049718 | GGGGGTCCCCTCCAC[A/G]TTCCATATTGTAAAC | 51317 |
rs183667120 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46114741 | TCAACTACTGTTTGA[A/T]TTGTAAGTATGTCGC | 51317 |
rs183677224 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46090433 | CTAAGGATAAGAGTC[A/G/T]TACAAAAAAGGAATG | 51317 |
rs183682025 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46067917 | GAGGAGTGTCTAACT[A/C]TGCTTGGAAGGTAGA | 51317 |
rs183689228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46046273 | ACAGGACAGTGCCAA[C/T]AGCACTGGGGCCATC | 51317 |
rs183728450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46045059 | GAAAAGTGTTAAACA[C/T]ACAGCAAAGTTCTTA | 51317 |
rs183731776 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PHF21A | GRCh38.p7 | 11:46074691 | TATTTTTAGTAGAGA[C/T]GGGGTTTTGCCACGT | 51317 |
rs183738877 | snp | A/T | | | missense, utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45979899 | TGTGGCAATGGCTGT[A/T]TTTGGAACTTGTCCG | 51317 |
rs183776009 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45956952 | ACACAAAAAGGTTGA[A/G]AGTGAAAGGATGTTT | 51317 |
rs183794952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46004569 | GACAGAATATTCTCT[A/G]TTCTTTTCTTCAACA | 51317 |
rs183824040 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | PHF21A | GRCh38.p7 | 11:46094673 | GGATCACGAGATCAG[A/G]AGATCGAGACCGTCC | 51317 |
rs183825077 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45964615 | CCAAATTCTTCTTTC[C/T]CATCACTAGTCGTTT | 51317 |
rs183828950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46071258 | ACTACAAAATGAATA[C/T]GCCCCAGGTAGCTGC | 51317 |
rs183832051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46051463 | CACAAAAGAGTTTAC[C/T]AGGCCTTCATTTCCA | 51317 |
rs183842706 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46029071 | CCTTTTCAAAACAAA[A/G]TGTAGCTTGCAAAAG | 51317 |
rs183844395 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:46008497 | GAGAAGTGCCAATGT[C/T]TTGAAAGCTACTCCA | 51317 |
rs183850086 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46093551 | AATTTTAATCACCAA[A/G]GTTAGGATGACTCTC | 51317 |
rs183866845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46027563 | ATTTGATTCAGTCTT[C/T]AATGCACACAACTCT | 51317 |
rs183908133 | snp | G/T | | | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45935739 | TTCTCTTCTTCTTTT[G/T]CTAAAAAAAAAAAAA | 51317 |
rs183911508 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45929279 | GGACTGGAATGTGTC[C/T]TGCCCACCCTCCCCT | 51317 |
rs183914141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45955175 | TTTTTGCATCCCTTT[A/G]TGCCTATTATGGTAC | 51317 |
rs183917223 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45952488 | CTTTGATAGGGAAAT[C/T]TTGCTCAATTTTTCC | 51317 |
rs183917955 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46102193 | AGCTCAAGTGATACA[A/C]CAGCCTCGGCCTCCC | 51317 |
rs183922127 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46010117 | AGTTTGAGAGTTACT[A/G]CAGGAATGAGAACAA | 51317 |
rs183923351 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46078486 | AATTATCAGAAGACA[A/T]GGTAAGTTTTTAGGA | 51317 |
rs183925297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45979407 | GCTAAGAATTCCAGA[A/G]GAGGTCAAGTCACAA | 51317 |
rs183933276 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | PHF21A | GRCh38.p7 | 11:46000928 | TCCGTCTCAAAAAAA[A/T]AAATAAATAAATAAA | 51317 |
rs183943587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46057582 | AAAGAGAGTTGGTAT[C/T]TCTTTTAAAATGTCA | 51317 |
rs183979766 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46005688 | TAAACATTAGGGGAA[C/T]CATCAGCACCAACTA | 51317 |
rs183999088 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46075695 | TATAAAGCAGTTGTT[A/C]ACTCAGCTTGGAAGA | 51317 |
rs184007414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45938825 | TTCAGATAAGGGGGA[A/G]ACTAGTGTATTCTTT | 51317 |
rs184018751 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46033135 | TCATGAAATTCTCCA[G/T]GTTGATACATATACC | 51317 |
rs184022149 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45988338 | AGTTTTCTTAGAAGA[C/T]AGAAAAAGACAATAA | 51317 |
rs184049603 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46070629 | AGCCACCGCACCCAG[C/G]CTGGTGACTATAATT | 51317 |
rs184054404 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45941844 | ACCAACTGCAATTTC[A/G]TCATGTGCTAAACAA | 51317 |
rs184065713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45967763 | TCGGTATGAATGTCT[A/G]ACTGAACTTAAAACG | 51317 |
rs184069029 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45991332 | CTGTTACATAAAAAC[A/G]AAGTAATAATATCAG | 51317 |
rs184070115 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45933582 | AAGTAAGGATCTGAA[A/T]CCTGCTCTCCTCCCT | 51317 |
rs184079599 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:46010907 | CAGCATCATACCAGC[A/T]CCTTTCTCTCCTACT | 51317 |
rs184146798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46065736 | TCCTTTTCTTTAACA[A/G]AAGTTGTTTAAGCGC | 51317 |
rs184149212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45934270 | GAGCCGCCTGGTTTC[C/T]AACAGGCCTGGCAGC | 51317 |
rs184153968 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46024248 | CTTCTCTGACTTTCC[C/T]ATTTCTCCCACTTAC | 51317 |
rs184161376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45958289 | AAAGACACCAAAGAA[C/T]AGAAAATGGGCTGGG | 51317 |
rs184162426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46055650 | ACCAAGTCTATACAT[C/T]ACATCATCAAAGGAA | 51317 |
rs184174793 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45985708 | TTAGACAAATAGTTT[A/C/T]TTTCCCTTTTTAACC | 51317 |
rs184226295 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46073189 | AAAAATTGGCCAGGC[A/G]TGGTGGCGGGCGCCT | 51317 |
rs184234709 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46052649 | ATTCATGAAGCTAAA[A/T]TGCTCCTAGCTGCTA | 51317 |
rs184240080 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46107917 | TAGTGGTTGAGTGAG[C/T]AGGGATAGGTGATGG | 51317 |
rs184241947 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46030469 | TATCAGATTTCAATA[A/C]CAGCATTTTAAAAAG | 51317 |
rs184242670 | snp | A/T | | | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46085221 | TATGATGTGGATATT[A/T]TAAAATGTATCTATC | 51317 |
rs184245621 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46061600 | TCCAAAGAAACTATA[A/C]AATGTCTCTCAATAA | 51317 |
rs184354468 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46077725 | CCTGTTGTCCAACAA[A/C/G]TTACTGTCCTGCCTA | 51317 |
rs184358292 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46108569 | AATGTGTGTGTGTGT[A/G]TATATATATATATAT | 51317 |
rs184361250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46056499 | TTTTAAAACAAGAAA[C/T]TGGGCTTTTAAAAAA | 51317 |
rs184370844 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46035690 | TTTTACACTGAGACT[C/T]GAAGGATGTGTATGA | 51317 |
rs184371544 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:46062093 | CTGTTTTTTGTTTTG[G/T]TTTTTTTTTTCCTCT | 51317 |
rs184379043 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46014428 | TGATGGACACCTAGG[C/T]TGATTCCATGTCTTT | 51317 |
rs184385276 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46019588 | GTTCTTTCTGATGCT[A/T]TAAATTGCACTCTAT | 51317 |
rs184450984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45946846 | AGACCGGCAAAGCAA[A/G]GAGGCAAAATTCAAG | 51317 |
rs184453159 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45973302 | TGAAAAGTACCTCCA[C/T]TCTTTCAGAAACACA | 51317 |
rs184462546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45994867 | TCACACGCTTTGAAT[A/G]TCTCCCTGGTATTTC | 51317 |
rs184467859 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | PHF21A | GRCh38.p7 | 11:45940434 | CTCCTGACCTCATGA[A/T]CTGCCCACCTCGGCC | 51317 |
rs184480690 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45990284 | TTTTTTTTCAAACAG[G/T]ATCTCACTCTGTCCC | 51317 |
rs184484640 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46086658 | AATTTTTACAAGGCT[A/C]TACCAGAAAATGTGT | 51317 |
rs184502334 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46042481 | GACTAAAATCACTGA[A/G]TGGTTTTTATAAATC | 51317 |
rs184563278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45973990 | AGCCTCAAACTCACC[C/T]GAATTATATACTTAC | 51317 |
rs184573590 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46030820 | TAGTGTGTGTGTGTG[C/T]GTGTGTGTGCGTGTG | 51317 |
rs184605261 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:45966548 | CAAATCCTAGTTCTA[C/T]CACTCACTAGCTGTG | 51317 |
rs184606108 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46042238 | ATGACAAAACATATT[C/T]CTCAATAAGGCATAT | 51317 |
rs184683899 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45947255 | GCCCTTGTCTTCTAG[A/G]GGCAAGGTCATTGCT | 51317 |
rs184689881 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45950552 | AAAATCGCAAAAAAA[A/C]CTCATGATGTTTTAA | 51317 |
rs184697579 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45941166 | TGCAGTGCTGTGATC[C/T]TGGCTTACTGCAGCC | 51317 |
rs184707264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46089666 | CTAGTTGGATGTTTC[C/T]ATACTATTAAATTAT | 51317 |
rs184719575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46115236 | GCTTTAGAAGAGTCC[A/G]AAGGATGGCTGAACC | 51317 |
rs184732938 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46045489 | CTACTATTACTCCAG[G/T]CTAATTACTTGCTAT | 51317 |
rs184751694 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45946675 | CCACCGCACCTGGCC[A/G]AATTTATTATTTTTT | 51317 |
rs184757143 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:45972175 | GAGTTTTAAAAGCCT[A/G]AGAGATCAGAAGATG | 51317 |
rs184828216 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46113173 | GCTCTAATCTGAAGT[G/T]AAGCAAAAACTGCAA | 51317 |
rs184830748 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46108899 | CCCACCCCATGCTAC[A/G]CACTATGCTTGGCAA | 51317 |
rs184835297 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:45951677 | GTGTGTGGACTGATA[C/T]TCAGATGCACCCTCT | 51317 |
rs184838873 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46086760 | CTTCATTCTACTGAC[A/G]GTAACATAAAACCAT | 51317 |
rs184844524 | snp | G/T | | | missense, utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:46076786 | CTGTGATTTTGGCTT[G/T]GAGTTCATGAAGCTG | 51317 |
rs184848700 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46037680 | AGGGTGCTTATCTGA[C/T]TCTTATCCTTTTGTA | 51317 |
rs184850381 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:46066524 | GCAACAAAATGAGAA[C/T]CTGTTTCTAAAAAAA | 51317 |
rs184885017 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:46042019 | GTGTTAAAAATGGCA[A/G]TTTTCCTACTATACT | 51317 |
rs184918284 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46116488 | CAACTACTATCACAT[C/T]ACATCAATGGAGAAA | 51317 |
rs184924550 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46093332 | TCATTGCCTCAGGGA[A/C]TATTTCAAAAGAGCT | 51317 |
rs184926431 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46070157 | CTATAGATCAGAAAC[A/G]TAACTAGTTATAGGA | 51317 |
rs184934119 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, utr-variant-5-prime | PHF21A | GRCh38.p7 | 11:46049454 | ATTCCTGTACAGTGG[A/C]ATCTGCAAGCCAAAT | 51317 |
rs184948194 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46027348 | TTATACATGTATAAG[A/G]GGTTTAACAGGTTTG | 51317 |
rs184951014 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45978428 | ACTGCCAGTATACAG[C/T]AACCTCTATTAAATG | 51317 |
rs184999881 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46007021 | CAGTTTTAATCTTTA[A/G]AGCGTTCCTGCAAGC | 51317 |
rs185000843 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PHF21A | GRCh38.p7 | 11:46018963 | CGTAAGCAGCAAGAA[C/T]ACACACATCATGTAA | 51317 |
rs185014024 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46024822 | AGAAAGAAAGAAAGA[A/C]AGACTTAGGGACTTC | 51317 |
rs185025534 | snp | G/T | 0.00795532 | 0.062565 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:46120948 | ACCCTCCTGCTGCTG[G/T]CTGGCTGTCCCCCCT | 51317 |
rs185084377 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PHF21A | GRCh38.p7 | 11:46053303 | AACAAATACCTAAAA[A/G]TAAAGGGTACTAACT | 51317 |
rs185089807 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46030765 | GTTTTTTTTTAATTT[C/G]TAACTTTAAGAAGGT | 51317 |
rs185094810 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45962308 | GATACGGGTTTGGTA[A/T]CTGTGAACAGGTGTG | 51317 |
rs185131852 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46079430 | CGGGTGACAGTGGCT[C/T]CCGAAAGGAATTTAA | 51317 |
rs185146942 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46097159 | TAACTGGCCTCCCCA[A/G]TTCTACCCTAGCCCC | 51317 |
rs185179985 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PHF21A | GRCh38.p7 | 11:46068604 | ATTCCACAAACTTGG[C/T]CTTTGATTTGATATT | 51317 |
rs185188165 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46101258 | AGACATCTTCAGTAA[C/G]TTAAAAGACAAATGA | 51317 |
rs185194730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46025912 | ACTTTTATTGTAGGC[A/G]AAGACATTTCAAAAT | 51317 |
rs185216341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45997532 | ATGCTGGTTTCTCAA[C/T]GTCTAGATCCAGTGA | 51317 |
rs185232195 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PHF21A | GRCh38.p7 | 11:45933181 | AAGGGCCAGTGGCCC[A/G]GGCTCTGCTTGTTCT | 51317 |
rs185234831 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45948429 | TCTCAAGTGTGGCTA[A/C]CTCTTTCCTTCCTGG | 51317 |
rs185249053 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45954910 | TCATTATGCTGGAAA[C/T]ATTTTACTAGATCTG | 51317 |
rs185251151 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46097522 | GTTTCAGGAGCAAAA[G/T]AATACTAAAATAAAG | 51317 |
rs185256898 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45982619 | ATGTAAATTTTATTG[C/T]TTGGTGACTGCTAGA | 51317 |
rs185259012 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:46044030 | ACAGCTGTAAATTTG[C/T]TTTTACCTTCATAGA | 51317 |
rs185262756 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46003702 | AGTATGGCTCAGCAC[A/G]CTACAGAGCACATGA | 51317 |
rs185264468 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PHF21A | GRCh38.p7 | 11:46073272 | GGCGGAGCTTGCAGT[A/G]AGCCAAGACAGCGCC | 51317 |
rs185266174 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46023087 | TATTTAGGCTAAGGT[A/C]TCAGACCTTGAGTGA | 51317 |
rs185293396 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45937856 | GTTTTAAAACCATAT[A/T]CTTGGTCTGGACCAT | 51317 |
rs185295222 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45961215 | TCCTGTTCTTTTTGG[C/T]ATAATAAAAGAATCC | 51317 |
rs185302170 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46047481 | CTGGATAAAGAAACC[A/G]AGACAAAAAGGTAAA | 51317 |
rs185308322 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45987889 | TGCTTTGTTAATATC[A/G]GAATTGTCTTGGACA | 51317 |
rs185316708 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46007670 | ACATTAAAAATAAAC[C/T]GCTAGCATGAATATT | 51317 |
rs185329003 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46112950 | TGATAAAAAATACAA[A/T]AAACTAATCTAAGGT | 51317 |
rs185331265 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46059312 | ATGATAGGATACTAT[A/C]AAGCCACTAAAAACT | 51317 |
rs185368758 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PHF21A | GRCh38.p7 | 11:45967231 | ACATTAGCCAGGCAT[A/G]GTGGCACACACTTGT | 51317 |
rs185376348 | snp | A/G | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46119744 | CGAACGTGGTCAGGG[A/G]AAAAAAAAAAAAAAG | 51317 |
rs185384972 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | PHF21A | GRCh38.p7 | 11:46010626 | TAATACTGCAAGTCA[A/T]CAATCACAAAACAAA | 51317 |
rs185404855 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46048468 | TGCTATGAACATCCA[C/T]GTAGAAATTTTTGTT | 51317 |
rs185414332 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46026872 | ATCTTTAAATGCCTG[C/G]CCCACCAAAGGTCTT | 51317 |
rs185453836 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46007172 | ACTGCATACCTACCA[G/T]GTGTTCAAAAACATG | 51317 |
rs185482565 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46092131 | TATTTGAATAACTAT[C/G]CAGCTAGCATCAGGA | 51317 |
rs185499253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45991063 | CCCTCACCCTCTGGC[A/G]ACCACTCCTCTTTTT | 51317 |
rs185505052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46095242 | AACTGAGCAGCAAAA[A/G]GCAAGATCTATACAC | 51317 |
rs185522068 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46052055 | CAAGGTTGAGATGAT[A/C]CAGGAGTAGCATATG | 51317 |
rs185610516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46083256 | GAACAAGAGTTTAAC[A/G]AGATCCGGAGCAGCA | 51317 |
rs185616333 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45994670 | AACAAGATGTCAGGG[G/T]TTTTGCTGTTGCATC | 51317 |
rs185618979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46119459 | ACTTCCAGACCTAAA[C/T]AAAGAATATTTCAAC | 51317 |
rs185638613 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46072297 | GGCCACATGACTAAG[C/T]TCAGGCCCATGGGAT | 51317 |
rs185661041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46029772 | CCAATAGTGCACCTA[A/G]CTTAAAAATAACAAA | 51317 |
rs185746152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45935431 | GATGTTACAGAGCTT[A/G]GGTAAGGCACCACCT | 51317 |
rs185766593 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45986257 | AATGCAGTTTTCTTA[G/T]TTAATTCACTCATGC | 51317 |
rs185798134 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46105216 | CTGCACTAACATTCT[C/T]AACCTCTGTGTTCTA | 51317 |
rs185815883 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:46013908 | CAGTGAATGAGTGGT[A/T]AGTAAATGTGAAAGC | 51317 |
rs185823050 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46080772 | TCCTGGGCTTCAGCA[A/G]TCTTCCCACCTTAGC | 51317 |
rs185828616 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45986429 | GAAAGAGTGTGGCTG[G/T]TGTACTCAAGAGAGA | 51317 |
rs185833518 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46038229 | CCTCCCAGTTTCAAG[C/T]GATTCTCCTGCCTCA | 51317 |
rs185866314 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PHF21A | GRCh38.p7 | 11:45963738 | ATAGTGTTGTGAAAC[A/G]AGGTTCTGTGGAACA | 51317 |
rs185880006 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46007899 | TTTAAAAAGGTACAG[G/T]ATCTATCACAATAAT | 51317 |
rs185926095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46099853 | CTCTCTGACTATACA[A/G]GTTTAGCTCCACAAC | 51317 |
rs185928547 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PHF21A | GRCh38.p7 | 11:46074763 | CCACCTTGGCCTCCC[A/G]AAGTGCTGGGATTAC | 51317 |
rs185938106 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:46104052 | TGACAATTAAATATA[C/G]AAAGAAAATAACAAC | 51317 |
rs185943929 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46054380 | GGAATAAAAATGCTA[C/T]GTCAAATTGGCTTGG | 51317 |
rs185945848 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46110182 | GTACATTCATGAGTA[G/T]TATCTTATCTAATCC | 51317 |
rs185959288 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46058934 | GACAGCAGAAATGAA[A/G]CAGAAGCAAAGAAAG | 51317 |
rs185973044 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:46015454 | TTCCAAGGTTTTCTT[C/G]TAGGATTCTTATAGT | 51317 |
rs185988671 | snp | G/T | 1.73183e-05 | 0.00294259 | intron-variant | PHF21A | GRCh38.p7 | 11:45938353 | AAAAAGGACAAAAAA[G/T]GTAAAATTTTAATGT | 51317 |
rs185999760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45988308 | GGATACCTTTTAAGA[A/G]TCCTCAACTCTGTAA | 51317 |
rs186002581 | snp | G/T | 1.64814e-05 | 0.00287061 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45935670 | TGTTTCACCTTTTGC[G/T]CTAGTTGTTCTCGTT | 51317 |
rs186082216 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46114661 | CCCAAAGTTTTGGGT[A/T]CTTATTTAAAATTTA | 51317 |
rs186082692 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46099560 | CACACACACACACAC[A/C]CACCCTAAACACAAA | 51317 |
rs186086565 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46061588 | TTTCCCATACTTTCC[A/C]AAGAAACTATACAAT | 51317 |
rs186095562 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46039266 | AGTATAGGTAGGGTG[C/G]AGAATTTGTTTCGAT | 51317 |
rs186104098 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46015553 | TAAAGTTTAATTTTT[A/G]AACTTTTTGACTCTT | 51317 |
rs186107087 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45943308 | TTGTATATTTAGTAG[A/T]GACGGGGTTTCACTA | 51317 |
rs186108898 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46111115 | AAATCACAACTATGT[A/G/T]GGGGGGGAGGCTAGT | 51317 |
rs186121322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45992183 | TTTTCAACCCTCAGA[C/T]GGTAATTACACTCAC | 51317 |
rs186129219 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46063654 | ACCCTGAAGTAATGG[C/T]TAAAACCACTTTACC | 51317 |
rs186244319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45967998 | CAAGTGGGTCATGAT[C/T]CACTGTTTGAAAAAC | 51317 |
rs186257089 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46088183 | ATATTTTGACCAATT[A/C]TAACAAGTTATAAAT | 51317 |
rs186259705 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46104621 | TCTCCAGCTAAATTG[G/T]TCCAAATTTACTCTT | 51317 |
rs186262048 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:46059301 | ACCCTACCCAAATGA[C/T]AGGATACTATCAAGC | 51317 |
rs186262987 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45975477 | CACATCTGTTTTATA[C/T]TATTTTGCTGGTTTA | 51317 |
rs186264288 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46011134 | ACTCCTTGAGGGAAA[G/T]AATTAACCGTTTTAA | 51317 |
rs186266489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46092512 | CATAGAAATGAAATG[C/T]ACCTCATTTAAATAA | 51317 |
rs186269740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45998095 | AGAGGCTAAAAAGAT[C/T]ACTGAATCCCAGAGG | 51317 |
rs186273040 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46082410 | TCATGATCAACAATC[A/G]TGTAGGTGACACCAT | 51317 |
rs186278116 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46059175 | ATTACGTACAAATAT[C/T]TACGTCCAAGGATGT | 51317 |
rs186280535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46016347 | GTAAGGCATTTAAGG[C/T]CCTTAACAACTATAC | 51317 |
rs186297697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45980319 | GCCATCCTACTTCAA[C/T]TCCAATTTCAGTTTT | 51317 |
rs186301913 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46001695 | CTGTGTGCATCAGAG[C/T]TAACTGGTATGATAG | 51317 |
rs186301931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45943934 | TCAGACAATCCAAAC[A/G]GAGAGGCATTCTACA | 51317 |
rs186309528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45970486 | ATCAAAATTTAGATA[C/T]ATTTCTCCCAAGCTT | 51317 |
rs186365705 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45998411 | TACTGAGTATATAGT[A/G]TTGTAACAGATGTAG | 51317 |
rs186392699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46062641 | TTCCCTTAAATATCT[A/G]GTGATTCTTGGCTAT | 51317 |
rs186399143 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46043356 | CATCTGAAGACACAG[A/G]TTACTTCTGTTTACC | 51317 |
rs186400568 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46088408 | CCTCTAACTTTCCAA[C/T]AACAACAACAACAAC | 51317 |
rs186402939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46019971 | TTTTAAGGGCATTTT[A/G]CTATTTTCTACATTT | 51317 |
rs186418177 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:46115787 | TCTCTGTTTGAATAG[C/T]AATTAAATACAAAAG | 51317 |
rs186430206 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46040105 | GTATGAACTGTGCCA[C/G]ATATAACAGGGTTAC | 51317 |
rs186438440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46068868 | TGATGCATCTGGTAC[A/G]AGTAACCAACTGACT | 51317 |
rs186465229 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:45953946 | CCTTTCTGATTTCCA[C/T]GTATTTTAGAATGTG | 51317 |
rs186502901 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45948392 | CTTAGTTGGAGATGC[C/T]CTCTTCTCAAAGATT | 51317 |
rs186508598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45975131 | CCAGCCTTGGCAACA[C/T]AGTGAAACTCCACCT | 51317 |
rs186516426 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46017214 | GACCTCAGGTGATCC[A/G]CTCGCCTCAGCCTCC | 51317 |
rs186587272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45950013 | GTTTTCCCAGGACAG[C/T]AGTGTGGATAATGAT | 51317 |
rs186594415 | snp | A/C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46087762 | TGAATATTTTGAAAA[A/C/G]ATTTTTTTCCTGAGA | 51317 |
rs186603738 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45976424 | CAGTGCTTGCACACA[C/G]TAGGAACTCCACAAA | 51317 |
rs186604386 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:46043619 | ACACGTTACAAAGTG[C/T]CAAAAGGGCCATTAA | 51317 |
rs186609558 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46071496 | ATTAAAGTGTAAGTT[A/T]CTTCATCAAGCTTAT | 51317 |
rs186610024 | snp | G/T | 0.0275645 | 0.114116 | intron-variant | PHF21A | GRCh38.p7 | 11:45999032 | GGGTTTCACCATGTT[G/T]GCCAGGCTGGTCTCA | 51317 |
rs186616503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46051540 | TGCCTAAGGAAACCT[C/T]AAACAGAGTACTCTA | 51317 |
rs186642463 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46019083 | GGAAGCCTAATCTAA[A/T]TTTTTTTTTTTTTTA | 51317 |
rs186655878 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45931618 | TGTTGCATTTGCTTT[C/T]AGATCTGTCTTTGTC | 51317 |
rs186668179 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PHF21A | GRCh38.p7 | 11:46003009 | AAAGATTGAATACTA[C/T]GATTTCTAACTGTTT | 51317 |
rs186747900 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45940649 | ACTATGATTTTCTTC[C/T]TTCATTATTAAAATC | 51317 |
rs186790516 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PHF21A | GRCh38.p7 | 11:46094884 | CAGCCTGGCGACAGA[A/G]TGAGTCTCCGTCCCA | 51317 |
rs186790824 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46118851 | AAGGAGGGGGCCAGT[C/G]TTCAAAGACCAAAAG | 51317 |
rs186836158 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46063393 | AAAAATAACCAGATA[G/T]TAACTACTGTAAGGC | 51317 |
rs186843186 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45957777 | AAAAAAAAGAAAAAA[A/G]AAAATAAAGTCTAGG | 51317 |
rs186848536 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PHF21A | GRCh38.p7 | 11:46022451 | CAAAGTGAGACCCTG[C/T]CTCTTAAAAAAAAAG | 51317 |
rs186872741 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45981808 | GAATCCAAATCTGTG[C/G]ATTACTCATTTAACA | 51317 |
rs186921458 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | PHF21A | GRCh38.p7 | 11:46117390 | GTAGCTATATTCATC[C/T]TTATGCAGTTACTGT | 51317 |
rs186931965 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46066908 | ACAAACACAGTTTTT[C/T]AGTATTTTGCATTTT | 51317 |
rs186933905 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45987799 | GTAACTGTCTGTTTA[C/T]AGAACACCGCTGCAC | 51317 |
rs186934414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46045952 | CTGTTTTCTTGCTTA[C/T]AGAGATAAAGTACCG | 51317 |
rs186935972 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46100302 | ATGAGCATGGACTTT[C/T]TTCCTAAGTCTCTTC | 51317 |
rs186940287 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46075409 | ATTCATTGGCGTCTT[A/C/G]TCAAACTAACCCTGA | 51317 |
rs186943158 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45967487 | CACATCCATTGTGGG[C/G]ACCTTGAAGCCATGC | 51317 |
rs186944384 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46024355 | TCCTTTCTCCCATGA[A/G]AGTGCTTTCTGCTTG | 51317 |
rs186946292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45948671 | CTGAGTCAGCTTTGC[C/T]AGAATCCTAGTAAAG | 51317 |
rs187038291 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45939842 | AATGCCTAGCTCATT[A/C]TCTGGATGGGATTAA | 51317 |
rs187046469 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45965828 | GCTTTTGATTCTAAA[A/C]CCTGAGCTCCCTCTT | 51317 |
rs187055129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45989222 | AAACCTGAACTCATC[C/T]TTCAGAATTTCAGAA | 51317 |
rs187061566 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46108422 | TGTATAAATCTTACC[A/C]ACCTCTCTTCCTCCA | 51317 |
rs187062762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46009599 | CAATCCTAGGAGATA[C/T]GTACTATATAGTATG | 51317 |
rs187076916 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | PHF21A | GRCh38.p7 | 11:46028784 | TCACCATGTTGGTCA[C/G]GCTAGTTTCGAACTC | 51317 |
rs187108741 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46098889 | CTGCATCTGTGAGAA[A/C]CCTTTCTATTGCACT | 51317 |
rs187120234 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46053899 | GCATGTGATGATTAC[A/C]ACCCCTCCAATGAGA | 51317 |
rs187120921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45959662 | TCCATAAAACAAATA[C/T]TAGAGCTAATAAACA | 51317 |
rs187134879 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46012298 | CCTCTCTGCTTTCCT[G/T]TCACCATCTGCTTAA | 51317 |
rs187202414 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PHF21A | GRCh38.p7 | 11:45952661 | GAAAGAATTACATTT[C/T]GTACTTGTTTTAGGA | 51317 |
rs187207830 | snp | G/T | | | missense, utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45979903 | GCAATGGCTGTATTT[G/T]GAACTTGTCCGGTTG | 51317 |
rs187234710 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45992634 | TTCTGACTAATCAAA[A/C]TTTTATCATAATGGA | 51317 |
rs187254555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46070949 | TTATCAATATATGCT[A/G]TTAATGTGATATAGC | 51317 |
rs187256135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46050968 | AAAAATTTACCTAAA[A/G]ATAAATATAGCAGTC | 51317 |
rs187267508 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45931277 | AAAAGGTAAGTTAGG[G/T]GTTGTGTGGCAACCC | 51317 |
rs187284849 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46073855 | AGGTCAAGAAGCTGA[A/C]TTTGAAATCTGCCAG | 51317 |
rs187295516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46031229 | TCCCTTCCAACCTCT[C/T]TCCATACCTTTTGTC | 51317 |
rs187392711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46032108 | AAAGGAGACACACCA[A/G]AGTTTGATTTAGATA | 51317 |
rs187395983 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:45999294 | CTAACTCAAGGAAAC[A/T]TTTTTGAGATTAAAA | 51317 |
rs187401648 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46013067 | TTTCCTATATATTCA[C/G]ACCTATGATAAAGTT | 51317 |
rs187442861 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | PHF21A | GRCh38.p7 | 11:45946404 | TTATTTATTTTTTGA[A/G]ACGGAATCTCGCTCT | 51317 |
rs187448260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46084006 | TTAAAAGCAGTATCT[A/G]TGACTTTGTCGAGTA | 51317 |
rs187451650 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:45970937 | CAGGACGCTTCTGTA[A/G]TGATTTGAGCAGATA | 51317 |
rs187459294 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45933889 | CACTTTCCAGAAATC[C/T]GGCTTTGCTTTTCTA | 51317 |
rs187459672 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:45993854 | GGGCAGCTGGCGAGA[C/T]AGCTCTGGAGCCTGT | 51317 |
rs187461223 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46040547 | TAAAAGACTGGATTA[C/G]TCATTACTGCAGTAC | 51317 |
rs187486859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46106792 | CCATCTCAATGGGAG[C/T]AGAAGCTATCAGGGC | 51317 |
rs187488979 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46084451 | TCCCTCAAAACAATT[A/C]TTCAAGTATTCCTCT | 51317 |
rs187504584 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45975392 | TAAAACAAAACAAAA[C/T]AAAATAAAACAGATG | 51317 |
rs187506938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46061317 | GATCCCATATGAATC[C/T]TAAAATAGTTTTCTC | 51317 |
rs187511760 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PHF21A | GRCh38.p7 | 11:46041778 | ATATACCCTTCCACG[C/T]TCCCTGAACTATCAC | 51317 |
rs187517682 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45990712 | GCAGTCCCTTGATTT[G/T]TTTTTTTTTTTTAAA | 51317 |
rs187518039 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46018593 | AAATGCCTTTTAAAT[A/C]CCACTAACCTATTTG | 51317 |
rs187530795 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46054048 | ACGTCGTGGCAGTGG[A/G]GGAAGAAAGTTGAAC | 51317 |
rs187555722 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | PHF21A | GRCh38.p7 | 11:45966584 | TGAGGTAACATACCT[C/G]ATTTTTAATAGCCAG | 51317 |
rs187569325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46010249 | ATGATTAAGTCACCT[A/G]AGACCAGGAACAGTC | 51317 |
rs187602755 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45994118 | GACAATTTTAAGATT[A/C]TGTTGCTAACCTTAC | 51317 |
rs187619487 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45946730 | GGTTTCTCTGCAATC[A/G]GCATTCTCACAATAC | 51317 |
rs187622514 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46004381 | GTAAAAAACTTGTAC[G/T]TTTGACCAAAGGAAA | 51317 |
rs187626192 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | PHF21A | GRCh38.p7 | 11:45972257 | GAAGCTGTACTTTTC[G/T]AGACTTTTTACTAGA | 51317 |
rs187639844 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45994678 | GTCAGGGGTTTTGCT[G/T]TTGCATCATTCTGCA | 51317 |
rs187649893 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46014124 | CCCACATGGTGAACA[C/T]AGTACCCAACAGGAA | 51317 |
rs187658272 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PHF21A | GRCh38.p7 | 11:46044324 | AAAAGAAAATTCATG[C/T]AAGGTAAAAGAAGTA | 51317 |
rs187666557 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:45939111 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGCACC | 51317 |
rs187674519 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45964644 | TTTTCAAATAGGATA[A/C]GGTGACTGCCTATAA | 51317 |
rs187683744 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PHF21A | GRCh38.p7 | 11:46023730 | GGAGACAGAGGTGGG[C/T]GGATCGCCTGAGGTC | 51317 |
rs187693243 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46113600 | TTTAGGAGGCTGAGG[C/T]GGGTGAATTACGAGA | 51317 |
rs187693442 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46105752 | AAATTTTACATTTAA[A/T]AAGCACTAGGCCTCT | 51317 |
rs187702489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46029413 | TCTTCACTGGCTGGG[C/T]GCAGTGGCTCACGCC | 51317 |
rs187712368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46060007 | CCTCGGCCTCCAAAG[C/T]GCTGGGATTACAGGC | 51317 |
rs187755711 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | PHF21A | GRCh38.p7 | 11:46032383 | TGCTACCATGTCCTT[A/C]GTTTATTTAATAATA | 51317 |
rs187774322 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:45946465 | CTCGGCTCACTGCAA[C/T]CTCCGCCTCCCGGGT | 51317 |
rs187787051 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46096300 | AATTAAAAAAAAAAA[A/C]CCTCTTGACTCCATA | 51317 |
rs187827155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45990801 | TTCCCACATACTCCT[A/G]GCCTCCCCACCCCAC | 51317 |
rs187830597 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46111481 | ACTCCGTCTCAAATA[A/C]ATAAATAAATAAATA | 51317 |
rs187839056 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45976169 | CATTTACTATTTTGA[C/T]GCCATCCTTTTGTTC | 51317 |
rs187844519 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46089068 | CAAACTGTCCCTAAA[A/C]AGGACAACTCCATGT | 51317 |
rs187850848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46064676 | GAATATATGATTTGG[C/T]CTGTCATTTAACATA | 51317 |
rs187867466 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PHF21A | GRCh38.p7 | 11:45972142 | CAATGAAACATGACA[A/C]GGTGAAAACAAACAT | 51317 |
rs187991639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46089853 | GGAATCTCTACACAG[A/G]TCATACCTCCACTGC | 51317 |
rs188030105 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PHF21A | GRCh38.p7 | 11:46055150 | AAGATACTTTGAAGC[A/G]ATCTGAATGTAGAAT | 51317 |
rs188046225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46013437 | TAATGGCCCCAAAGC[A/G]AAAGAGTAGTGATGT | 51317 |
rs188057611 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46094436 | AGAGCTTATGGGCCC[G/T]AGATTCCTTGGCTGA | 51317 |
rs188092989 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46042923 | TTTCTGTTATTTATA[A/C]ATGATCCAGTCTGAG | 51317 |
rs188099159 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46019700 | CAATGAAATTTAGTC[A/G]TATTAGTCTCCGGTT | 51317 |
rs188111239 | snp | A/C/T | 4.94176e-05 | 0.00497059 | synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45949417 | CTCTGGCTCAAAGAC[A/C/T]GCTCCACTGTAGACC | 51317 |
rs188112262 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PHF21A | GRCh38.p7 | 11:46097627 | TTTTACCCTCTCTCT[A/G]ACTATCCAAATCTCA | 51317 |
rs188118280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46073517 | CGTAATTTATTGTGG[A/G]GCATTTAGAAAATAT | 51317 |
rs188132362 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45961644 | AATTGACGACATGTT[A/T]CATAGAAGTCTTTGT | 51317 |
rs188181739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46089295 | ACTATGTATCTAATA[C/T]GTAGGTAGATAAAAT | 51317 |
rs188195248 | snp | G/T | 0.185487 | 0.241533 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45965336 | TTCAAGACTTGGCTT[G/T]CTAAGCTGTACAGTT | 51317 |
rs188206309 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46045173 | TGGAGCAAAGTCCCA[A/G]TTGGGTTCCCAAGCT | 51317 |
rs188238313 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45929461 | GCACAAAACTCCAAA[C/T]ACAAGTCTACCAAGA | 51317 |
rs188254588 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:45952544 | AATTCTGTGGATGAT[C/T]TCACAAGTTCCTCAG | 51317 |
rs188262658 | snp | C/T | 0.000395387 | 0.0140548 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45979946 | TATCAGGTTCTTCCG[C/T]AGCTGTTCAACTACT | 51317 |
rs188269058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46001293 | TGACCACCAGGGGGG[C/T]TGGAAATGGGGCTCT | 51317 |
rs188279512 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46066038 | CTGTGAATCTGTAAT[A/T]ATTTCCAAGTAAAAA | 51317 |
rs188297957 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PHF21A | GRCh38.p7 | 11:45934406 | ACCTAAGGAACAGGG[C/T]GGGTGGAGTGGGTAG | 51317 |
rs188298152 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45958445 | ATATATATATATATA[C/T]ATATACACACACACA | 51317 |
rs188310009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45956988 | GAATGGCTATAGTAC[C/T]ATTAGACAAAAGTGA | 51317 |
rs188312612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45985711 | GACAAATAGTTTCTT[C/T]CCCTTTTTAACCTCT | 51317 |
rs188319010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46006380 | TCAAATCCAGAATTA[A/G]TAAGCACCTAACGAA | 51317 |
rs188331916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46004980 | ATAATATTTGTCTCT[C/T]ACTGCAAATGTCTCT | 51317 |
rs188375803 | snp | A/T | 1.64806e-05 | 0.00287054 | missense, utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45979869 | TGCTGTGCTGTTTGT[A/T]GTTTGTTTTCAGATT | 51317 |
rs188439317 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45950475 | TTGGAAGAAGAAGAA[C/T]TGTCTCGAGCCACAC | 51317 |
rs188465813 | snp | G/T | | | upstream-variant-2KB | PHF21A, LOC105376661 | GRCh38.p7 | 11:46123020 | AATACAAATGGGGGG[G/T]TGGGGGGTTTTGTTT | 51317 |
rs188471320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46112430 | CACCGTGCTAGGTAC[A/G]GTCATAGATTTTAAC | 51317 |
rs188485312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46065554 | ATAAATTCACTTACT[A/G]TCTTAGCCACTTTTA | 51317 |
rs188499257 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46024095 | GAAAGCAAGGAAAGG[A/G]CAAGGTGGTGTCTGG | 51317 |
rs188540353 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46070653 | TATAATTTTTAAACA[C/G]AGTCAGAGAAGGAAA | 51317 |
rs188548397 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | PHF21A | GRCh38.p7 | 11:46079433 | GTGACAGTGGCTTCC[A/G]AAAGGAATTTAAGCA | 51317 |
rs188561788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46027999 | TTTCACTACAGCCTA[A/G]TAATACAAACAGGGT | 51317 |
rs188575771 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46095198 | ATTGTCAAAAAAAAA[A/G]CAAATATTCTATTTC | 51317 |
rs188576836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45988348 | GAAGACAGAAAAAGA[C/T]AATAATATTAGAAAA | 51317 |
rs188585929 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:46097481 | TCATGGCTCACTCCC[A/T]CAAATTATTGAGGAA | 51317 |
rs188589215 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:46073249 | GGGAGAATGGCGTGA[A/C]CCCAGGAGGCGGAGC | 51317 |
rs188603529 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46053177 | GTGTCCTGATAAATG[A/T]TTGGTTTCACAGAAC | 51317 |
rs188607192 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45984590 | CAGAAAATCAGGTTC[A/G]TTTTTCCACCGTTTA | 51317 |
rs188607945 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46030470 | ATCAGATTTCAATAC[C/T]AGCATTTTAAAAAGA | 51317 |
rs188624326 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45933625 | GCTCCCCACCCAAGA[A/G]AACAGAAACAAACCC | 51317 |
rs188640768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45984059 | AAATGTAGCTAACTA[C/T]ATTGGAACATTATCC | 51317 |
rs188650640 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:45967809 | CTACTGACTTAACAG[G/T]AAGAAATATATTTTA | 51317 |
rs188658918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45991380 | GGTAGAACAATGAGG[C/T]TCTGAGTAATTAAGT | 51317 |
rs188666476 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46008894 | TGACCAGTGTTCACC[A/C]TCCATCTTAATCAGA | 51317 |
rs188668997 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:46010908 | AGCATCATACCAGCT[A/C]CTTTCTCTCCTACTA | 51317 |
rs188674065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45977370 | TCAAACTCCTGACCT[A/G]AAGTGATCCACCCAC | 51317 |
rs188698988 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45932148 | AGGGCTGATGCAGCC[A/G]GCCTGTACTCCCGCA | 51317 |
rs188746719 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46056562 | AGAATGGAGACAGGA[G/T]AAATTAACAGCTTCT | 51317 |
rs188757326 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | PHF21A | GRCh38.p7 | 11:46036882 | TTATGTTTAAAAAAA[A/T]TTTTTTTTGTAGAGA | 51317 |
rs188765421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46014480 | ATGAACATACAAGTG[C/T]AAGTGTACTTTTTGG | 51317 |
rs188819079 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46093830 | AATTTCTTATGCATC[A/G]ATTTCCAGCAGCATT | 51317 |
rs188833660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46049988 | GACCATATTCTATCA[C/T]ATATTTCATGTAGTC | 51317 |
rs188840064 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46101207 | AGCTAAAATCTGTCC[A/G]GCAGGCATCGTTCTT | 51317 |
rs188858145 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PHF21A | GRCh38.p7 | 11:46055785 | ATAGCAGGGGATTCA[C/T]TGAAAATATAATACG | 51317 |
rs188909117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45995019 | TATATGCAGACCTGG[A/G]AGAAAGACCTAATTG | 51317 |
rs188916155 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45956185 | GGGAGTCCCTTCAGG[C/G]TGAAATGAAAGGACA | 51317 |
rs188917045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45960759 | CCCTTCGATGAATCT[A/G]AAGTTTGGTCTCTGA | 51317 |
rs188920264 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:46101682 | TTGTTGCCCAGGCTG[C/G]AGTGCAGTGGCATGG | 51317 |
rs188935961 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46077973 | CTGGAGTGCAGTGAC[A/C]AGATCTTGGCTCACT | 51317 |
rs188960277 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:45941470 | GTAAACCCCACTGTT[C/T]GGTCTTGAGAGAATG | 51317 |
rs188974876 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45991198 | GTTCTTCTATGTTTT[G/T]CATGGTTTGATAGTT | 51317 |
rs189134651 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46076417 | GGTAACAAGGTACAC[A/G]CAGCACCTACAAGAT | 51317 |
rs189139810 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46049554 | AGGGTGTGGCGGGGG[A/G]AGGAGGGATAGAAAG | 51317 |
rs189146935 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46033676 | GCTATCTATCCACTA[C/G]CCATATATGGCTATT | 51317 |
rs189157967 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46086685 | GTGTCCAAAATGATT[C/G]CTTATAATTTTTGTC | 51317 |
rs189170898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46087001 | ACTAAGATTATATGC[C/T]TTGTCTATCAAACTG | 51317 |
rs189185640 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46062717 | CTCTCATACACTACT[C/G]AAAGGAATGTAAAAT | 51317 |
rs189189230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46043564 | TGAAGTGATAAAGAC[A/G]AGCTCTGCCAAACTG | 51317 |
rs189198480 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45977858 | CTTTTTTTTTTTTTG[G/T]TATTGAATGGCAGTA | 51317 |
rs189199941 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46021423 | CAAGTATACACCATA[C/T]CTCCATCAGTATTGT | 51317 |
rs189207112 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45947738 | GGGGGGCTCCTTTCC[A/G]AGAACTGCATCAGGG | 51317 |
rs189221333 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45996586 | GTGCCAGGAATGCTA[C/T]TCTCCATATGCACAA | 51317 |
rs189286168 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46079324 | GTGATCCATGTAATA[C/G]GCTCAGGAGACACTT | 51317 |
rs189302861 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46037818 | TTTTTTTCCTCCAAA[A/T]TTTCTTGCTTGATGC | 51317 |
rs189334236 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46097017 | ACACTCCACATCTAC[C/T]CCGACAGCCAACCAT | 51317 |
rs189357689 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46109111 | ATTTCTAGGTATCTA[A/T]GGGAATTACATAGTT | 51317 |
rs189399641 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PHF21A | GRCh38.p7 | 11:45940448 | ATCTGCCCACCTCGG[C/T]CTCCCAAAGTGCTGG | 51317 |
rs189424842 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46108605 | ATACATATGTAAATG[A/C]ACAGGAAAAGTTTAA | 51317 |
rs189445269 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46062281 | TATATTAGTTATTGG[C/T]TGGTTTTCTCTTCTC | 51317 |
rs189467147 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45943031 | CATAACCTATATTCA[A/C]TCCTGATGGCTCTTC | 51317 |
rs189495076 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45974027 | CCCAACACTTTAAAA[A/C/G]CACTGAAACCTAACA | 51317 |
rs189514193 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46114754 | GATTTGTAAGTATGT[C/T]GCTTTGGAGATGCAC | 51317 |
rs189520255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46038288 | ATGTGCCACCACACC[C/T]GGCTAATTTTTGTAT | 51317 |
rs189520466 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46091819 | CAGCTTCCTAAGTAA[A/C]TGGAGCTATAGGCAC | 51317 |
rs189521263 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45955119 | TTCCCCCTTTATACT[A/C]AACGCTATGTAAGAG | 51317 |
rs189522149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46068193 | TCACATGGAAGTAAC[A/G]CTGCCAAGATTTTCA | 51317 |
rs189526687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46015501 | TTATTTCTTCAATAA[C/T]AAATTAACCTTAGCT | 51317 |
rs189530995 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45983004 | GCCTAGCTAAAGTAC[A/C]CTAGAAGCAAGAAAC | 51317 |
rs189536036 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46046994 | AACAGCTTTACCTCT[A/G]ATAAAGTTTAAGCTA | 51317 |
rs189541671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46003815 | ATTTGCCCTTCATCA[A/G]TTGCTTCCTATGCCA | 51317 |
rs189578708 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46057619 | ATATGACTCAAGCTG[A/C]AATAAGTAAAATCAC | 51317 |
rs189597803 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46015015 | ATAAAAAAATAAAAA[A/T]AAATAAAAAAATAAA | 51317 |
rs189650353 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46061994 | GCTTTTCAGAATTTG[C/T]AAAGCATCATTCCAA | 51317 |
rs189671260 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46019035 | ATAAGGCAAGAAAAA[C/G]AAAGGGGGAAGAAAA | 51317 |
rs189672508 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46063761 | TATATATAATTTTAT[A/C]AGCTATTAGCAGGAA | 51317 |
rs189676511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46044231 | TCAAAAGCTGTCCTA[C/T]AGTACAGCTAGAGGT | 51317 |
rs189687053 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46023510 | TCAGCATTCCTAAAC[G/T]GTGTCATATGGAATA | 51317 |
rs189712482 | snp | A/C | 0.00557542 | 0.0525036 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PHF21A | GRCh38.p7 | 11:45933409 | TGATACACTGTCCCA[A/C]CCCCTGCTCCCTCCA | 51317 |
rs189723193 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45966197 | TATGTACTGAAGACT[C/T]ACACTTTTACCTCAG | 51317 |
rs189733267 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45951975 | CTGCATCCAGCTAAT[A/T]TTTGTATTTTTAGTA | 51317 |
rs189758386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45937953 | AAATACAAGGAAGCA[C/T]CTATCCAGCTCAGTA | 51317 |
rs189763825 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45962511 | GAGTCTCTGCTGATC[G/T]GGCTCGGTAACCTCT | 51317 |
rs189775644 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45987909 | TGTCTTGGACACTAC[A/C]GAAATTCTCCCATTC | 51317 |
rs189784228 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46007698 | ATTAAATCCGTCATT[C/T]TAAAATTTAGTTACA | 51317 |
rs189815183 | snp | C/G/T | 0.00954224 | 0.0684493 | intron-variant | PHF21A | GRCh38.p7 | 11:46068937 | TAATGTGGCACGTTA[C/G/T]TAAAGTATAAGTTAC | 51317 |
rs189819122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46048940 | TAACATTTTACATTC[C/T]CACCAGCAATGTCTG | 51317 |
rs189830155 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46027173 | TCTCACATCACTCTG[A/C]TTTTTCTCCCTGATT | 51317 |
rs189882449 | snp | C/T | 0.0244538 | 0.107838 | upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46121988 | CAGCGGCGGCGGCGG[C/T]GGCGGTGATGGGGCC | 51317 |
rs189912463 | snp | C/T | | | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46085316 | TTCAAGCTTGCCAGT[C/T]ATCTCTTTGACTATA | 51317 |
rs189947555 | snp | A/G | 0.0191293 | 0.0959101 | intron-variant | PHF21A | GRCh38.p7 | 11:45999860 | GTATATAGAAACATC[A/G]TAACTTTTCTCTTGA | 51317 |
rs189976873 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46047826 | GCATGTGAAAACTCT[C/G]GGTAAACAATGGCAC | 51317 |
rs189980772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46007598 | GGTATTACAGGTGTG[A/G]GCCACCGTGCCCGGC | 51317 |
rs189999807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46092596 | CATTAACAAATTAAG[A/G]TAACATCACTAGTTC | 51317 |
rs190034579 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45952679 | ACTTGTTTTAGGAAA[C/T]CTGAACTGGCTCAAT | 51317 |
rs190092193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46119607 | GCACCCGACAACCGG[C/T]CTGTGGCCTTCTCCG | 51317 |
rs190118495 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46072705 | GGAAGGAGTGTCAGG[G/T]ATAGCTCCTCTGAGG | 51317 |
rs190133761 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:46030302 | TTATTTTTTCTCTCC[A/G]TAAGTTCTCTTGCTC | 51317 |
rs190150494 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45999857 | CCAGTATATAGAAAC[A/G]TCGTAACTTTTCTCT | 51317 |
rs190197709 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:45946871 | TTCAAGTTAACTATT[C/G]TTATCCCTTGCTTTT | 51317 |
rs190203499 | snp | A/G | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46119759 | GAAAAAAAAAAAAAA[A/G]AAATCCTAACAGCAC | 51317 |
rs190210216 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46115575 | GAGAAAATTAATGTG[A/G]TCAAAACGTTAAAGA | 51317 |
rs190218211 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46068816 | ACGTTATTAGGATAA[A/G]CTTACAAGAGGATTG | 51317 |
rs190220677 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45931811 | GCAAAGGTCTCCAGC[A/G]AGAGCACAAATCTGA | 51317 |
rs190224790 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45954138 | AGTACCTGGGATTAC[A/G]GGCACCCGCTACCAC | 51317 |
rs190226643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45987808 | TGTTTACAGAACACC[A/G]CTGCACATACCATCA | 51317 |
rs190236993 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | PHF21A | GRCh38.p7 | 11:46026850 | AAGAATGCTGAGAAG[G/T]CCTTACATCTTTAAA | 51317 |
rs190257488 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | PHF21A | GRCh38.p7 | 11:46074770 | GGCCTCCCAAAGTGC[C/T]GGGATTACAGGCGTG | 51317 |
rs190261731 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PHF21A | GRCh38.p7 | 11:46055115 | TTCCATTTTGGACTT[C/T]TAAATTATGGCGAGA | 51317 |
rs190269515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45935447 | GGTAAGGCACCACCT[A/G]CCAACTGGCCGCCTG | 51317 |
rs190272470 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45929939 | CAGAGGGACAGGGGC[A/G]AGGTTCACACAGAGC | 51317 |
rs190279949 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46013277 | TAAGTTTTAAACTGC[A/C]CGCTTAGAGTAGCCT | 51317 |
rs190284754 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46010684 | GGTTTTCTAAGCCAG[C/T]GTGCAAAGCCTTGAC | 51317 |
rs190290833 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45980605 | ACAGCCTTGAACTCC[G/T]GGCATCAAGCAATCT | 51317 |
rs190362497 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46096802 | AGCACATATCCTTCC[C/T]CTGAATTCCAAACTC | 51317 |
rs190372877 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46052458 | GAGTCTTCACTCATA[C/T]ACCTACTGAATACCT | 51317 |
rs190402174 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PHF21A | GRCh38.p7 | 11:45993967 | CTGGGCAGGGCTAGA[C/T]AACTTGCTTCAAAGT | 51317 |
rs190414464 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45936751 | AAATATCAGCTTAGG[A/G]GAATCAAGTTCAAGG | 51317 |
rs190415992 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46104133 | AAATGCCCAAAATCA[G/T]AAAGCAAATAAACTG | 51317 |
rs190435917 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46059105 | GAAAGTTATGAAGAA[C/G]CATCTATTTATGTAT | 51317 |
rs190436739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46100099 | CACAAAGAAACAGGA[A/G]TCTGAAACATGCCTC | 51317 |
rs190458081 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46067651 | AATTTTCTTTTGATG[G/T]TGAACCCTTGGTAGG | 51317 |
rs190465076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46025097 | AATAAACACACACTG[C/T]CTATCCACAAGGAGC | 51317 |
rs190473933 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:46009430 | ACCTGCCTAGAATGA[A/T]CTGTGAAACCCTATT | 51317 |
rs190487872 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:45986903 | TGGCTATTTTTTTTT[A/T]AATGACAACTGCCAA | 51317 |
rs190534385 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45959058 | ATTAAAAGGATGGTA[C/T]ACTATGACAAAGCCA | 51317 |
rs190583044 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46104633 | TTGTTCCAAATTTAC[C/T]CTTTTCCCATGAACT | 51317 |
rs190587444 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46082663 | CTTTTGAGTCAACAA[A/C]TGTAAATTTAAAATT | 51317 |
rs190591725 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46011775 | CAGAGGGGAATTTTA[C/T]GAGTTTTTATTTACT | 51317 |
rs190604752 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46059178 | ACGTACAAATATTTA[C/T]GTCCAAGGATGTACA | 51317 |
rs190608809 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46039323 | TCTGCTGATTCTCTT[C/T]ATAGAACTGGTAATT | 51317 |
rs190618487 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46015728 | TTAGCCTAGGCCTAC[A/G]CAGGGTCACAATCAT | 51317 |
rs190670915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46080936 | CCAGAGTAGCTGAGA[C/T]TACAGGCGTAAGCCA | 51317 |
rs190696830 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45944699 | CCCCCAGATCCTCCC[A/G]AGGCTTCACCACTCT | 51317 |
rs190697244 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45957819 | TGAAATAGAGAAGAA[A/C]AACAGACTCAACAAA | 51317 |
rs190700109 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46109562 | AACACAAAAGCTCAT[A/T]ATTAAAATTTTTCAT | 51317 |
rs190702699 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:45970527 | CAGTTTTCTAAATGG[C/T]TTGATCCTAGAACTC | 51317 |
rs190713131 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45992683 | TAGTGGGAAAATGCA[G/T]AGACAAAAGGCAAGT | 51317 |
rs190731345 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46088526 | TATCTGGAAAGCACA[C/T]TCACCATCCCAAAAA | 51317 |
rs190749414 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46007052 | TCGTTTTACAGGTGA[C/T]TTCCCATTACAAAAA | 51317 |
rs190750234 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46012525 | AGCTATTTGGTCTTA[C/T]GCAAGTTAACTCACG | 51317 |
rs190756958 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46111634 | TGCCCTGCTTCTGCA[A/T]ACATTCAAACTAAGA | 51317 |
rs190758045 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | PHF21A | GRCh38.p7 | 11:46053561 | TATGTATACCATGAC[G/T]GGTAAAAAGAACCCC | 51317 |
rs190761011 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PHF21A | GRCh38.p7 | 11:46089097 | GTTCTCTATACCATG[C/T]ATTTATTTGGTGTGA | 51317 |
rs190765137 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46064708 | TCAACATTTTAAAAA[A/G]GAGAAATCCAAAACA | 51317 |
rs190772260 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45970053 | ATTAACACTGCATTA[C/G]GAAACTTTTTAACTC | 51317 |
rs190777553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46044776 | CTTCTACAAGATAAA[A/G]CACTGATTCAATTCT | 51317 |
rs190854456 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:45949558 | CATTGTTTTATCTAT[C/T]GGTTTTCCCATAAGA | 51317 |
rs190866906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45998474 | CCACATCTATTTTAG[A/G]AAACAGAAGATGTAC | 51317 |
rs190899684 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PHF21A | GRCh38.p7 | 11:46093383 | ATCTTTGTTTAACCA[C/T]GTACAGTTATACCAA | 51317 |
rs190901741 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | PHF21A | GRCh38.p7 | 11:46116982 | AAAAAATAAAAAAAT[A/T]AAAAAACTATAGTGT | 51317 |
rs190915085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46070528 | TAGAGACAGGGTTTC[A/G]CCATGTTGGCCAGGC | 51317 |
rs190963431 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46111245 | AGGCCGAGGTGGGCA[G/T]ATCACTTGAGGCCAA | 51317 |
rs191004519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45943312 | ATATTTAGTAGAGAC[A/G]GGGTTTCACTATATT | 51317 |
rs191014378 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46031057 | TACAGGAAATTCATG[C/T]ACGACAAGCGATCAC | 51317 |
rs191024644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45992256 | AAAATTTTTCAGCCC[A/G]GCATGGTGGCTCATG | 51317 |
rs191058111 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:46116034 | TCAAAAGAATAGTCA[C/T]TTCTAAAATTTAAGA | 51317 |
rs191059969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46083263 | AGTTTAACGAGATCC[A/G]GAGCAGCAGCAGGGA | 51317 |
rs191069313 | snp | G/T | | | missense, utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45979874 | TGCTGTTTGTAGTTT[G/T]TTTTCAGATTGTGGC | 51317 |
rs191075459 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46040338 | TGATGACACTACTGG[C/T]AGTTATAAACAAAGA | 51317 |
rs191107645 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45976197 | TTCATACTACTCTCT[A/G]TACTTGTGAAGCTCT | 51317 |
rs191132016 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46016349 | AAGGCATTTAAGGCC[A/C]TTAACAACTATACTT | 51317 |
rs191143440 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PHF21A | GRCh38.p7 | 11:45948596 | TGGGGTTCTGTTCAC[C/T]GTGCTATTCATGGAT | 51317 |
rs191155538 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45975218 | ACTTGAGAGGCTGAG[A/G]TGGAAGGATCACCTA | 51317 |
rs191163495 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45997978 | TCTGAACACTGGGCT[C/T]GTAAGGAGGATGGCA | 51317 |
rs191207094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46110391 | TTAAAAAAGAAAACT[A/G]TGTTCAATAATTTAG | 51317 |
rs191220225 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46063470 | AAGCAGTCAGTCATA[C/G]AGAATATGTAAATGT | 51317 |
rs191234728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46022553 | TGCAGCCTCAAACTC[C/T]TGGGCTCAAGCAATC | 51317 |
rs191277165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45985929 | AATTGACAACAGCAG[C/T]AACTGTAATTATCAG | 51317 |
rs191286992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46006733 | GTATTAAGTATTGAA[C/T]TGTCTTAAACGCCTA | 51317 |
rs191288602 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46105390 | CACAGGACATGCCCC[C/T]GATGATTAGATCACT | 51317 |
rs191306900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46059310 | AAATGATAGGATACT[A/G]TCAAGCCACTAAAAA | 51317 |
rs191317704 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45981898 | GTTCTCTTGAGAGTT[G/T]TTTGTTTTTATTTTT | 51317 |
rs191325526 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45946426 | TCTCGCTCTGTCACC[C/G]AGGCTGGAGTGCTGT | 51317 |
rs191331153 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46090043 | TATACACATTCTTCT[A/G]TTTCCTAACTTTCTT | 51317 |
rs191345477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46067848 | TGCAAATAAGTACCA[C/T]AATGAGCGCCAAATA | 51317 |
rs191351717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46046061 | CAGCTTTGTGAGCTC[C/T]GGCATTCAGCTAGCC | 51317 |
rs191351763 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46100587 | GTTAAGTAAGTATAC[C/T]CCTTGCACTAAATGA | 51317 |
rs191358284 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PHF21A | GRCh38.p7 | 11:46024804 | GACTCCATCTCAAAA[A/G]AAAGAAAGAAAGAAA | 51317 |
rs191383663 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PHF21A | GRCh38.p7 | 11:45975998 | AATATATGCCATATA[C/T]AACCTCCCATTTGTC | 51317 |
rs191440553 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46087932 | GGCTAATTTTTGTAT[C/T]TTTTTGTAGTGACAG | 51317 |
rs191463810 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:46043780 | GAGATGAGAGGACCC[C/T]GCTGTCATATACCCA | 51317 |
rs191490205 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PHF21A | GRCh38.p7 | 11:46017575 | TTCAGGATTTGCCCT[C/T]AAGGGGGAAAAAAAA | 51317 |
rs191516429 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46094279 | ATAAAGAATTTTGCC[A/C]TGATATCCTGAAATC | 51317 |
rs191526961 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46050056 | GCAATTAAAAGAAAA[C/T]TAGCAAGTCTTTCCC | 51317 |
rs191562906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46003527 | ACTTGATTTTTAAAA[C/T]ACCATAAAGCTGCCC | 51317 |
rs191571015 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45971873 | GGCTGGGGTAAAAGG[A/T]CAGTGTCTTTTTCTT | 51317 |
rs191635096 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45998369 | TAGGCAGTATAAGGT[C/T]TGAAGACAATATTAA | 51317 |
rs191652816 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46117908 | TTATGAATGGAATTT[G/T]TAAATGGACTTACTC | 51317 |
rs191656309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46094636 | GTGGCTCATGCCTGC[A/G]CTCTGGGAGGCCAAA | 51317 |
rs191659643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46071174 | CTAATGAGATGTTAA[C/T]AAACCTGATGCCAGC | 51317 |
rs191668664 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46051441 | TCCATTCTCATACCA[C/T]CTTGGGCACAAAAGA | 51317 |
rs191675991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46028824 | TCGTCCACTCGCCTC[A/G]GCCTCCCAAAGTGCT | 51317 |
rs191678492 | snp | A/T | | | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46119111 | AGTGCACAACTGCTT[A/T]AAAAAAAAAAAACTT | 51317 |
rs191695337 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46032045 | CAAAGCCCAACTCTT[A/C]AGTGCTGCTTTAAAA | 51317 |
rs191696160 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45989306 | GAGAGGTTCAGCATT[G/T]TAGAAGAAAAGCATG | 51317 |
rs191699060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45952210 | GGCAGTGATTCTGTC[C/T]AACTAGAAGGTGAAC | 51317 |
rs191703474 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46009707 | AGCAGACTTCCAACT[C/T]GGGCAGTTTGGCTAC | 51317 |
rs191709976 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45978796 | CTTTTTGTGTATCTT[A/G]ATTGCCTCACGATTC | 51317 |
rs191732233 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46108557 | AACTTCTTTAAAAAT[A/G]TGTGTGTGTGTATAT | 51317 |
rs191763653 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46087552 | ATTTGAAATTCTTTT[C/T]CTTTTCTTCAGAAAG | 51317 |
rs191776721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46070758 | GAAAGAACAACAAAA[C/T]TTAAAACCAAAAGAT | 51317 |
rs191798218 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46028189 | CCTATCCCAAAAATT[G/T]CAACATTCCAAAGAG | 51317 |
rs191828200 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45949100 | AAGGGTTTTATTGTA[G/T]GTACTTGGCTCTCAG | 51317 |
rs191845560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46101797 | CATGCCACCACACTC[A/G]GCTAATTTTTGTATT | 51317 |
rs191858453 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46078325 | AACTTGATTTTACTT[G/T]ACAGTGAAGCCTGTA | 51317 |
rs191858932 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:46056690 | GGCTCTCCCAATCAA[C/T]GAATCAGGATTTAGC | 51317 |
rs191867985 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | PHF21A | GRCh38.p7 | 11:46037435 | TCACCTGAGGTCAGG[A/G]GTTCAAGACCAGCCT | 51317 |
rs191872503 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46074082 | GAACTAGTGTCTACC[A/G]CAAGAAATAGTGACT | 51317 |
rs191874553 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46014660 | CCATAGCCTCTCCAA[C/T]ATCTGTTATTTTTGA | 51317 |
rs191903911 | snp | C/T | 0.000182377 | 0.00954754 | missense, utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934077 | GTGCAGTCCGGGCCA[C/T]TGGAGATGGCCCCCA | 51317 |
rs191918382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45957257 | AAAAGGACATAGGGA[A/G]CTTGAACAACACTAT | 51317 |
rs191922923 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45985315 | AGAAGAGGGGATGTG[C/T]TACTGTCATAACATT | 51317 |
rs191964525 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45939244 | GTAGAGGACAACCTA[C/T]ATATCATAAATCTTA | 51317 |
rs191966573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45965166 | ATGACCCTTCTGCAC[A/G]TGGATGAATTATCGC | 51317 |
rs191993426 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46061708 | AACCTAAACTGGCTG[G/T]TTTCTAAACCTGTTG | 51317 |
rs191995893 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46027368 | TAACAGGTTTGCACT[C/G]CTGCATTTTTCTGTT | 51317 |
rs191998539 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46107008 | TACCAACTGTCCTCC[A/T]GCTGTCCCCACGGCT | 51317 |
rs192003721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46085160 | TAACAAATTAATACT[C/T]AAAACAGACAAATAC | 51317 |
rs192017753 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46061580 | ATTAATTCTTTCCCA[A/T]ACTTTCCAAAGAAAC | 51317 |
rs192022276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46041809 | ACATCTTTCTTCTCC[C/T]ATGAACCATCTGAAA | 51317 |
rs192053474 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45940652 | ATGATTTTCTTCCTT[C/T]ATTATTAAAATCAGG | 51317 |
rs192067671 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45938573 | TGGATGCCTGAAACC[A/T]CCGTACTGAACCCTA | 51317 |
rs192078513 | snp | G/T | | | missense, utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45979910 | CTGTATTTGGAACTT[G/T]TCCGGTTGTTCTTGC | 51317 |
rs192081124 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45988337 | AAGTTTTCTTAGAAG[A/T]CAGAAAAAGACAATA | 51317 |
rs192102965 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45983397 | ATAGCGTTGGTATGT[A/C]AAACTGCCACTCAGA | 51317 |
rs192119247 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46075523 | AATCACATTCAGAGC[A/C]AAATACATACTAACC | 51317 |
rs192160990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45972166 | CAAACATCTGAGTTT[C/T]AAAAGCCTGAGAGAT | 51317 |
rs192162344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46099403 | GAGGATGAGCAAAAC[C/T]AACTAAATAAAAATT | 51317 |
rs192170222 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PHF21A | GRCh38.p7 | 11:45934663 | GAGCTCTCCAGGGTG[C/G]AAAACACACAGTGCT | 51317 |
rs192185367 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46054034 | CTTTTTCACAAGCAA[C/T]GTCGTGGCAGTGGAG | 51317 |
rs192196743 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45946733 | TTCTCTGCAATCAGC[A/C]TTCTCACAATACTTT | 51317 |
rs192252328 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46055336 | ATAATAGTTAATTAA[A/C]TTACAGTAACAAGAA | 51317 |
rs192322758 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46049632 | TGTCACAGCACTCTC[C/T]TTGCTGGTTGCCAGC | 51317 |
rs192364967 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46034844 | AGGGGATAGTGGGCA[C/T]GTGACCCTGGCCACA | 51317 |
rs192371857 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46014253 | CCCACTTATAAATGA[C/G]AACATATAATATTCA | 51317 |
rs192404413 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | PHF21A | GRCh38.p7 | 11:45973267 | ACATCACAGAAAGTT[C/G]TATCACTGTGCAATA | 51317 |
rs192412201 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:45994822 | ATATTCACTGGCAAC[A/G]TGACACACTAGTAAC | 51317 |
rs192415184 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45966325 | ATCTTCTCTTCCTCC[A/G]ATAATTGCCTCAGTA | 51317 |
rs192436479 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45963986 | GGCAGGTCACTTGAG[A/G]TTGGGAGTTTGAGAT | 51317 |
rs192458973 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46008418 | AAAATTCCTCTCTTG[C/G]TTTCCTGAAGGACTC | 51317 |
rs192493544 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46060199 | GATGGGGTCTTGCTA[A/C]GTTGGCCTGGCTGGT | 51317 |
rs192512137 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46041052 | AGGTCGCCCTCACTG[A/T]CTTTTCATGGTGAAT | 51317 |
rs192521219 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46017719 | CAAATGCAAATGATT[C/T]TGTCCCTAAAAACTG | 51317 |
rs192539534 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45946491 | CGGGTTCAAGCCATT[C/G]TCCTGCCTCAGCCTC | 51317 |
rs192553069 | snp | C/T | 0.0876345 | 0.190099 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46086229 | GTTCATGCCATTCTC[C/T]TGCCTCAGCCTCCTG | 51317 |
rs192557847 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:45994551 | GTGACGCAGCCATCA[A/C]TTCTGCTTAGTCTCC | 51317 |
rs192575247 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46042417 | TCATCACCACTTGAG[A/C]TGGTCTACGCTGAGG | 51317 |
rs192648579 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46000253 | ATTATTCACTTCTAC[A/G]CTATATGCCAAGGAA | 51317 |
rs192655307 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45950362 | AGCCCAATGGGCGGG[A/T]CTCATGAATGCACAA | 51317 |
rs192655802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46075657 | AAGACAAGATGGGGA[C/T]GCATAAGAATAGGAG | 51317 |
rs192662841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45976439 | GTAGGAACTCCACAA[A/G]TATTTACAGAATGAA | 51317 |
rs192668534 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46119343 | TGATGAGGCCCACAC[A/G]TGCCCGGACCTTCAC | 51317 |
rs192669300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45999170 | AACAAAGAAAATTAT[C/T]AGAAAATTTAAAAAC | 51317 |
rs192669930 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | PHF21A | GRCh38.p7 | 11:46094961 | AATGGGCTTCAGAGG[C/G]GTCTGTCAACTGCTT | 51317 |
rs192673551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46033116 | TTGTATTTTTTCCCA[A/G]GTCTCATGAAATTCT | 51317 |
rs192700184 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46046403 | ATGGCAAAAGAGAAA[A/C]CAAAAACTAAAACAA | 51317 |
rs192712036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46024105 | AAAGGGCAAGGTGGT[A/G]TCTGGGGATATCTCC | 51317 |
rs192718094 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46079429 | ACGGGTGACAGTGGC[C/T]TCCGAAAGGAATTTA | 51317 |
rs192750358 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45962307 | GGATACGGGTTTGGT[A/C]ACTGTGAACAGGTGT | 51317 |
rs192757314 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45939899 | GGAAGACTGAAGGGA[A/G]GTGCTAGAGGTGACC | 51317 |
rs192760271 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PHF21A | GRCh38.p7 | 11:46114277 | GCTAGAATTTACATA[C/T]ATACAGTTGCTACAC | 51317 |
rs192795272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46112814 | GGCTTCTCATGCCCA[C/T]ACTAGCAATGAATGA | 51317 |
rs192799478 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46065776 | TGAAGCACTAGGGTA[C/T]AAAGCGGGTGTATAA | 51317 |
rs192822861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45978396 | GGAGTATGTCCATTA[C/T]GTAAAACACTTAGGA | 51317 |
rs192828694 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46108463 | CACTTCCCACATGAG[A/C]CCTATTTTCAAAAAT | 51317 |
rs192835366 | snp | A/C | | | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46119629 | CCTTCTCCGGGGGTG[A/C]AAGCCACAGACAAAG | 51317 |
rs192838812 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46062072 | ATTCCCAATCCCTGT[C/T]TGCAACTGTTTTTTG | 51317 |
rs192845304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46019185 | TTTCGCTTTATCTTC[C/T]CTAAAGAGGAAAAGA | 51317 |
rs192855245 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46022145 | ATGTACTGTTTGTTT[C/G]TTTCTTTTTTTATTT | 51317 |
rs192874774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46018832 | TCACTTAATGGCACT[A/G]CTTACTGCATACCAT | 51317 |
rs192913067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46045354 | GAGGCTGAAAATATA[C/T]TTCCTGGCTGATTAA | 51317 |
rs192946120 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45956610 | TGGGGTTAATTCAAA[C/G/T]TAGATTGTTAAAAAC | 51317 |
rs192947111 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46097020 | CTCCACATCTACTCC[A/G]ACAGCCAACCATGTG | 51317 |
rs192968851 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46006509 | AAATAACAAGGAGTC[A/T]AAAAGTTTACTGCCA | 51317 |
rs193002042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46005087 | CATCAGTAATTTCAC[C/T]TTCTGCAGGCTCAGT | 51317 |
rs193003139 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46089615 | GGTAAGGCTGCTATG[C/T]TAAAATTCTGGTGTG | 51317 |
rs193009513 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PHF21A | GRCh38.p7 | 11:45933035 | ACACACACCTGGGTC[A/G]CGTGCTGCTTCACTC | 51317 |
rs193024895 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46077602 | CCTGCTTGGTCTTCT[C/G]TCAGGGTTAGGGAAC | 51317 |
rs193025277 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:45951651 | CTAACTGTTGTTCTT[C/T]TGATGAAGCAGTGTG | 51317 |
rs193034258 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45999588 | TTAAAAATATATCTA[C/T]AGAGGACAAAAAATG | 51317 |
rs193052497 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46004554 | TTTATCAGTAGCTAT[A/G]ACAGAATATTCTCTA | 51317 |
rs193141452 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:45941144 | GGCTCTGTCACCCAG[A/G]CTGGAGTGCAGTGCT | 51317 |
rs193146008 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46071552 | TTGACCAGTTAGGTA[A/T]AAGTACTGGCAGTGT | 51317 |
rs193147755 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45990863 | AGAACATTTGTTACA[A/G]TCGAACCTACACTGA | 51317 |
rs193150987 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46106158 | GGCATCTGTTCCAAG[C/T]ACAGCATGCTAACAT | 51317 |
rs193161257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46029507 | AGCCTGGGCAACATG[A/G]TGAAACCCTGTCTCT | 51317 |
rs193172065 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45933776 | GGTCCAATCTTTGCA[C/T]GTACACACAGAATAA | 51317 |
rs193174046 | snp | A/C/G | 0.00636936 | 0.0560724 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46119840 | ACTGCGTGCACGACG[A/C/G]GGCTGGACCAAACGG | 51317 |
rs193177827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45984200 | TGGAAAGAACAAAGA[C/T]GGAAGGGAGAGAGGG | 51317 |
rs193190178 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45947338 | AGGGCCAGAGAGATA[A/C]AAAACTGCCTATAAG | 51317 |
rs193214259 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:46101220 | CCAGCAGGCATCGTT[A/C]TTCACTAAGTTAGTG | 51317 |
rs193218489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46056244 | TTTTCATTAAGTCTT[C/T]CTCAAGAGAGTCAAT | 51317 |
rs193226314 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46023766 | TTTGAGACCAGCCTC[A/G]CCAACATGGTGAAAC | 51317 |
rs193297446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45966682 | TGGAGTGCAGTGGCG[C/T]GACCTCGGCTCACAG | 51317 |
rs193299849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46051682 | CTTGAAGGAAGAGAA[C/T]GGTCATCATGCCTCA | 51317 |
rs193301047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46010535 | ATTGTTTGGGAATAG[C/T]GGTATGAATAACTCA | 51317 |
rs193302389 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46084053 | GACATGACTCTTGGA[C/G]AAAATTGTCTTAAAG | 51317 |
rs199528573 | in-del | -/ATG | | | intron-variant | PHF21A | GRCh38.p7 | 11:45961639 | CTCTGAATTGACGAC[-/ATG]TTACATAGAAGTCTT | 51317 |
rs199531698 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46026644 | AAATGCAAAAAAAAA[-/A]TCCTTTAAAGTCAAG | 51317 |
rs199541583 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46015028 | AAAAAATAAAAAAAT[A/T]AAAAATAGTTATTCT | 51317 |
rs199576324 | snp | A/G | 0.00135589 | 0.026002 | intron-variant | PHF21A | GRCh38.p7 | 11:46076720 | TCTTTAGAACACAAC[A/G]TTAAAAATATGCCCC | 51317 |
rs199611691 | in-del | -/G | 0.0185938 | 0.0946107 | intron-variant | PHF21A | GRCh38.p7 | 11:46023573 | CTGAAAAAGAGGTTA[-/G]GTAAGTTTACCAAAT | 51317 |
rs199654625 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46044303 | CCTTAAATGAGCAGG[-/A]AAAAAAAAAGAAAAT | 51317 |
rs199703750 | snp | A/G | 0 | 0 | synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45935716 | AACTCCATTTAAGTA[A/G]CTTCTGTTTCTCTTC | 51317 |
rs199731971 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46108586 | ATATATATATATATA[A/T]AAAATACATATGTAA | 51317 |
rs199772789 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45987250 | GACTGTATCATAAAT[A/G]AATGTATGTATGTAT | 51317 |
rs199773972 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46078478 | ATAAATATAATTATC[A/C]GAAGACAAGGTAAGT | 51317 |
rs199788684 | snp | C/T | 0.000115307 | 0.00759211 | intron-variant | PHF21A | GRCh38.p7 | 11:45948883 | ATACAAAAAGGTCCT[C/T]ACCTCTCTTCCGGGT | 51317 |
rs199802844 | snp | C/T | 0.000149513 | 0.00864489 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934070 | AGGGGGGGTGCAGTC[C/T]GGGCCATTGGAGATG | 51317 |
rs199825140 | in-del | -/GTGTGTGTGT | | | intron-variant | PHF21A | GRCh38.p7 | 11:46030831 | TGTGCGTGTGTGTGC[-/GTGTGTGTGT]GTGTGTGTGTGTGTG | 51317 |
rs199856574 | snp | A/G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45982450 | TGCAGAATAATAAAA[A/G/T]TGCAAATTAATAAAA | 51317 |
rs199860171 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46095188 | CCATTTGGAAATTGT[A/C]AAAAAAAAAGCAAAT | 51317 |
rs199880109 | in-del | -/AAAATAAAATAAAATAAAAT | | | intron-variant | PHF21A | GRCh38.p7 | 11:45975323 | TGTCTCAAAGAAAAC[-/AAAATAAAATAAAATAAAAT]AAAATAAAATAAAAT | 51317 |
rs199945884 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45983644 | GAGGCCCTGCAGGCT[C/T]TTCCAAGGACTGGGA | 51317 |
rs199951563 | snp | A/G | 0.000132345 | 0.00813358 | missense, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45945941 | AGTCAGGATGACTGG[A/G]TTGGGGGGATGTTGG | 51317 |
rs199964791 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45975342 | TAAAATAAAATAAAA[C/T]AAAATAAAATAAAAT | 51317 |
rs200011860 | in-del | -/ATAT | 0.00993419 | 0.0697739 | intron-variant | PHF21A | GRCh38.p7 | 11:46068723 | TAGCCCAGTGTCAAC[-/ATAT]ATAACACCTGATGAC | 51317 |
rs200048370 | in-del | -/CCT | | | intron-variant | PHF21A | GRCh38.p7 | 11:45989837 | ACCCTGTCTCTACAA[-/CCT]AAAATACAAAAATTA | 51317 |
rs200063673 | snp | C/G | 0.00065136 | 0.0180348 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45933924 | CTTCAGTGTTCTGTT[C/G]TCCTTGCCGCCGGGA | 51317 |
rs200068069 | in-del | -/CAGC | | | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45932143 | CACCAAGGGCTGATG[-/CAGC]CAGCCTGTACTCCCG | 51317 |
rs200100464 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45990725 | TTGTTTTTTTTTTTT[A/T]AAGAAGACTTTATTT | 51317 |
rs200108521 | in-del | -/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45976635 | CACTTGAGCTCCGGA[-/C]GTTTGAGACCAGCCT | 51317 |
rs200112268 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46110569 | ATATTTTCTATATTG[C/G]CCATTAACACCAGGG | 51317 |
rs200169232 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45981940 | TCTCTTTTTGTTTTT[C/T]TTTTTTTTTTTTTTT | 51317 |
rs200194466 | snp | A/G | 0.000444719 | 0.0149051 | intron-variant | PHF21A | GRCh38.p7 | 11:45948859 | AAAAGCAACAGCAGC[A/G]AGGGAGAGATACAAA | 51317 |
rs200196294 | in-del | -/T | 0.0379877 | 0.132479 | intron-variant | PHF21A | GRCh38.p7 | 11:46062450 | TTTTGTTTTCCAACC[-/T]TTTTTTTTAAATCAA | 51317 |
rs200198960 | in-del | -/AAAAC | | | intron-variant | PHF21A | GRCh38.p7 | 11:45975372 | AAAATAAAATAAAAT[-/AAAAC]AAAATAAAACAAAAC | 51317 |
rs200215482 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45986110 | ACACACACACACACA[C/G]AGGTATTTACATCAA | 51317 |
rs200231857 | in-del | -/AAC | 0.0347861 | 0.127212 | intron-variant | PHF21A | GRCh38.p7 | 11:46088409 | CTCTAACTTTCCAAT[-/AAC]AACAACAACAACAAC | 51317 |
rs200274699 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45958443 | ATATATATATATATA[C/T]ATATATACACACACA | 51317 |
rs200282795 | in-del | -/AA | | | intron-variant | PHF21A | GRCh38.p7 | 11:45957752 | AACTAAATTCAAAGC[-/AA]AAAAAAAAAAAAAAA | 51317 |
rs200291138 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45944096 | CTGAAGCAGGAAAAA[A/C]AAAGTGTCACAAAAG | 51317 |
rs200299045 | snp | A/C | 0.00199806 | 0.0315443 | intron-variant | PHF21A | GRCh38.p7 | 11:45935621 | TCGACTGCTGAAGGC[A/C]TGAGGTTTACTTACA | 51317 |
rs200340010 | in-del | -/T | 0.0524604 | 0.153226 | intron-variant | PHF21A | GRCh38.p7 | 11:45982389 | CTCTCTGAGTAAATA[-/T]TTTTTTTTAAATGAT | 51317 |
rs200356197 | in-del | -/T | 0.204189 | 0.245767 | intron-variant | PHF21A | GRCh38.p7 | 11:46032479 | CAAATACACCAAATG[-/T]TTTTTTTCAATTCTC | 51317 |
rs200409253 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45968227 | AATTTATTCTCTGCA[C/T]AGAGGCAAGAAGGAA | 51317 |
rs200410948 | snp | C/T | 3.29647e-05 | 0.00405971 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45935641 | GTTTACTTACACTTA[C/T]GGAATTGCTGAGCTG | 51317 |
rs200420666 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46114150 | AAAGAACACTTAGAA[A/G]AACAGTATTCCAACT | 51317 |
rs200425880 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46015031 | AAATAAAAAAATAAA[A/T]AATAGTTATTCTGAC | 51317 |
rs200459741 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46113825 | GTGAGATTCATTCTC[A/C]AAAAAAAAAAAAAAA | 51317 |
rs200504325 | in-del | -/AC | 0.00478085 | 0.0486577 | intron-variant | PHF21A | GRCh38.p7 | 11:45991557 | CTGCAGTAAGCTTAT[-/AC]ACACACACACACACA | 51317 |
rs200548180 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46019081 | CTGGAAGCCTAATCT[A/T]ATTTTTTTTTTTTTT | 51317 |
rs200586865 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46099992 | ACTGCTATCCTTAAT[C/G]AACATTTATCTTTTT | 51317 |
rs200599552 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45987251 | ACTGTATCATAAATA[A/T]ATGTATGTATGTATG | 51317 |
rs200621220 | in-del | -/C | | | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46120335 | GAGGAGCCCCAGCTA[-/C]CCTCCCCGGCCGAGG | 51317 |
rs200626824 | in-del | -/C | 0.0573587 | 0.15934 | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45929391 | TCAGCTGCTCTGTAT[-/C]CCCCCCCCACCCCCT | 51317 |
rs200675961 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45977895 | AGTAGTTGAATGGAC[A/C]TATTTTTCAGCCAGA | 51317 |
rs200709354 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45970582 | TTCCTCCTTAAAGGG[A/T]TTTTTTTTTTTTCCT | 51317 |
rs200756167 | in-del | -/TA | 0.0310518 | 0.120672 | intron-variant | PHF21A | GRCh38.p7 | 11:45948096 | TTTCTAGCCTGCAAC[-/TA]TATAATTCAGGGACA | 51317 |
rs200779604 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45940198 | GATTTTAATCTTTTT[C/T]TTTTTTTTTTTTTTA | 51317 |
rs200842546 | snp | A/G | 6.5912e-05 | 0.00574035 | missense, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45971183 | GTGACCTTACTAGAC[A/G]TCTGGAGGTTGACTG | 51317 |
rs200885533 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45964179 | CTCCAGCCTGGGCAA[C/T]AAGAGTGAAACTCCA | 51317 |
rs200890179 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46118436 | AAAAAAAAAAAAAAA[C/G]CCCCTGGAATATTCG | 51317 |
rs200912466 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46069512 | GTATTAGAGGCTGGA[A/G]ATAGTCATATATCAG | 51317 |
rs200941157 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45998611 | CCACCTCCCAGGTTC[-/G]AAGTGATTCTCCTGC | 51317 |
rs201036024 | snp | G/T | | | upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46122539 | GTTCTTTTGTTCTAA[G/T]GGGGATGATGGCATT | 51317 |
rs201084175 | snp | C/T | 0.000624334 | 0.0176572 | synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45965558 | TGCGAGCATGGGAGG[C/T]GGTGCTGGGGCAATA | 51317 |
rs201119569 | in-del | -/A | 0.0178098 | 0.0926698 | intron-variant | PHF21A | GRCh38.p7 | 11:45974023 | TTAACCCAACACTTT[-/A]AAAACACTGAAACCT | 51317 |
rs201121653 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46015027 | AAAAAAATAAAAAAA[-/T]AAAAAATAGTTATTC | 51317 |
rs201149103 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46083169 | AACAGAAGCAAAGTT[A/T]AAAAAAAAAAAAAGT | 51317 |
rs201159425 | snp | C/T | 7.00611e-05 | 0.00591825 | intron-variant | PHF21A | GRCh38.p7 | 11:45938107 | ATTCCTCCTGATGGC[C/T]GTGTCTTTGTCCTCC | 51317 |
rs201187984 | in-del | -/TTTTTTTTTTTTT | | | intron-variant | PHF21A | GRCh38.p7 | 11:45990251 | AGCATTTTCATCTTC[-/TTTTTTTTTTTTT]TTTTTTTTTTTTTCA | 51317 |
rs201221455 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45962534 | TAACCTCTAAGACTA[A/G]TATGCCAGGCTGCCC | 51317 |
rs201229795 | snp | C/G | 0.000264162 | 0.0114896 | intron-variant | PHF21A | GRCh38.p7 | 11:46079180 | TTCTGGTAATAAAGA[C/G]AGAAAAAGAGCCATC | 51317 |
rs201236542 | snp | G/T | | | upstream-variant-2KB | PHF21A, LOC105376661 | GRCh38.p7 | 11:46123028 | TGGGGGGGTGGGGGG[G/T]TTTGTTTTTAAAGCT | 51317 |
rs201250058 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46101013 | ACAAGAAGGAAGTGC[-/G]GAACAAGACTTGTGA | 51317 |
rs201256842 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45951825 | TTTTTTTTTTTTTTT[G/T]AGGCGGAGTCTCACT | 51317 |
rs201263397 | snp | A/G | 0.000399281 | 0.0141238 | missense, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45945958 | TGGGGGGATGTTGGG[A/G]TAAGGGCTCCAAACC | 51317 |
rs201273053 | in-del | -/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46007321 | TTTCTTCTTCTTCTT[-/C]TTTTTTTTTTTCGAG | 51317 |
rs201274088 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45957439 | ACATAAAATCTCTTC[A/C]CCAGCCACAATGGAA | 51317 |
rs201277471 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45966196 | CTATGTACTGAAGAC[C/T]CACACTTTTACCTCA | 51317 |
rs201296262 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45986697 | AATTAATGGTGGGGA[A/T]TGCTTAGGAAACTGT | 51317 |
rs201322815 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46092095 | GAGAGCCTATTTGCC[A/C]AAAAAAAAAAAAAAT | 51317 |
rs201386236 | in-del | -/C | 0.00636936 | 0.0560724 | intron-variant | PHF21A | GRCh38.p7 | 11:46116319 | GATATACATCTTTTT[-/C]CACTGTGAAACAAGC | 51317 |
rs201402902 | snp | C/G/T | 0.0001154 | 0.0075953 | intron-variant | PHF21A | GRCh38.p7 | 11:45936487 | GTGGGTATGGATAAC[C/G/T]CCTTACCTGCTTTGT | 51317 |
rs201494316 | in-del | -/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45962232 | GAATGATGTTATCAT[-/C]TAAAGGGAATAGCAG | 51317 |
rs201509628 | in-del | -/T | 0.386417 | 0.209501 | intron-variant | PHF21A | GRCh38.p7 | 11:46110789 | TCTACATATTAACAA[-/T]TTTTTTTTTTTTTTG | 51317 |
rs201548405 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46035505 | CCTTGAATAGGCAGG[G/T]GGAGTCCTGACTCTC | 51317 |
rs201551932 | in-del | -/ACACACACACACACAC | 0.0265607 | 0.112138 | intron-variant | PHF21A | GRCh38.p7 | 11:45955284 | GTCTTTCTCTCTCCA[-/ACACACACACACACAC]ACACACACACTTTTT | 51317 |
rs201560749 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46030830 | GTGTGCGTGTGTGTG[C/T]GTGTGTGTGTGTGTG | 51317 |
rs201561875 | in-del | -/ATCTATCT | 0.28853 | 0.247013 | intron-variant | PHF21A | GRCh38.p7 | 11:46015896 | TGCTGTTTTACAGTC[-/ATCTATCT]ATCTATCTATCTATC | 51317 |
rs201568164 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46019083 | GGAAGCCTAATCTAA[-/T]TTTTTTTTTTTTTTA | 51317 |
rs201583561 | in-del | -/TA | 0.00636936 | 0.0560724 | intron-variant | PHF21A | GRCh38.p7 | 11:46034287 | TTCATAAGAACTCTT[-/TA]TATGTAAGACTAATA | 51317 |
rs201588912 | in-del | -/G | | | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46120342 | CCCAGCTACCTCCCC[-/G]GGCCGAGGGACAGCC | 51317 |
rs201598869 | snp | C/G | 0.00199799 | 0.0315437 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45965474 | GGGGTGGATGGAATT[C/G]TGGGATGTGGGAAGG | 51317 |
rs201604131 | in-del | -/CT | | | intron-variant | PHF21A | GRCh38.p7 | 11:45966194 | TCTATGTACTGAAGA[-/CT]CTCACACTTTTACCT | 51317 |
rs201623034 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45999057 | GTCTCAAACTCCTGA[C/G]CTCAAGTGATCTGCC | 51317 |
rs201635943 | snp | A/T | | | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46119557 | TACCCTCATCACAAC[A/T]ACTCAACTACTTAGA | 51317 |
rs201644980 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45976633 | GATCACTTGAGCTCC[-/G]GAGTTTGAGACCAGC | 51317 |
rs201659362 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45940662 | TCCTTCATTATTAAA[A/T]TCAGGCTGAGGGCTA | 51317 |
rs201681285 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46037642 | TGAAACGTCATCTCA[A/G]AAAAAAAAAAAAAAA | 51317 |
rs201686192 | snp | A/C | 1.65042e-05 | 0.0028726 | intron-variant | PHF21A | GRCh38.p7 | 11:45936469 | GGGGAAGCTTACAAA[A/C]AAGTGGGTATGGATA | 51317 |
rs201689293 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:45983494 | CTGTTGCTATCTGTG[-/A]AAAAAAAAAAATTTT | 51317 |
rs201717253 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46003285 | AAAGGCTAACATTCA[A/C]AAAAAAAAAAAAATG | 51317 |
rs201744847 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45964200 | TGAAACTCCATCTCA[A/T]AATAATAATAATAAT | 51317 |
rs201791025 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46069513 | TATTAGAGGCTGGAG[A/T]TAGTCATATATCAGG | 51317 |
rs201837972 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45953751 | TGTGGAACATATTAA[C/T]AAAAAGGTTAGTATT | 51317 |
rs201847139 | in-del | -/GTGTGTGTGTGT | | | intron-variant | PHF21A | GRCh38.p7 | 11:46030831 | TGTGCGTGTGTGTGC[-/GTGTGTGTGTGT]GTGTGTGTGTGTGTG | 51317 |
rs201895719 | in-del | -/AA | | | intron-variant | PHF21A | GRCh38.p7 | 11:46003284 | TAAAGGCTAACATTC[-/AA]AAAAAAAAAAAAATG | 51317 |
rs201896668 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45981934 | TGTTTCTCTCTTTTT[G/T]TTTTTCTTTTTTTTT | 51317 |
rs201920627 | snp | A/G | 1.67646e-05 | 0.00289517 | intron-variant | PHF21A | GRCh38.p7 | 11:46079118 | ACAATTAAATGAATA[A/G]CAATAGTAGTTTTAC | 51317 |
rs201935651 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46094717 | GAATAATAATTATTT[C/T]GTAGAAGTCTCTACT | 51317 |
rs201941105 | in-del | -/AGCCA | | | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45932144 | ACCAAGGGCTGATGC[-/AGCCA]GCCTGTACTCCCGCA | 51317 |
rs201951727 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46110803 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTTGC | 51317 |
rs201978704 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:45962686 | GCCTGAGGTCAGGAG[-/A]TCTGAGACCAGCCTG | 51317 |
rs201995682 | snp | A/C | 0.00299544 | 0.0385843 | intron-variant | PHF21A | GRCh38.p7 | 11:46084113 | ATGGACTTGTTTACT[A/C]ATCTTAGCCATTACT | 51317 |
rs202003023 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45998614 | ACCTCCCAGGTTCAA[-/G]TGATTCTCCTGCCTC | 51317 |
rs202030833 | snp | C/T | 0.00384513 | 0.0436782 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45933943 | TTGCCGCCGGGATCC[C/T]GTGGCTTCTCCTAGA | 51317 |
rs202068536 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45940655 | ATTTTCTTCCTTCAT[G/T]ATTAAAATCAGGCTG | 51317 |
rs202073249 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46105615 | CTTCCCAAACACCAT[-/A]AAAAAAAAACACAAA | 51317 |
rs202099254 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46026843 | CATCACGAAGAATGC[C/T]GAGAAGGCCTTACAT | 51317 |
rs202114215 | in-del | -/AAGA | 0.00676609 | 0.0577691 | intron-variant | PHF21A | GRCh38.p7 | 11:46098487 | TTTTTTATGGTTGAG[-/AAGA]AATAGCAGAAATAAA | 51317 |
rs202161942 | in-del | -/ACTACTCTAT | | | intron-variant | PHF21A | GRCh38.p7 | 11:46107491 | TGGTAAAAAACGTTG[-/ACTACTCTAT]AGTTTAAATAAACTG | 51317 |
rs202187902 | in-del | -/A | 0.0178098 | 0.0926698 | intron-variant | PHF21A | GRCh38.p7 | 11:46059645 | GCCTAGGTTGGTCTC[-/A]AACTGGCCTCAAAGG | 51317 |
rs202204983 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46112757 | AACTATCCCCATTTT[-/A]AAAAAAAAGGAACAG | 51317 |
rs202214058 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:45981872 | CTAAAATCTTTAAGT[-/A]AAAAAAAAAAGTTCT | 51317 |
rs202239805 | snp | C/T | 0.000562318 | 0.0167584 | synonymous-codon, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45945942 | GTCAGGATGACTGGA[C/T]TGGGGGGATGTTGGG | 51317 |
rs367617789 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PHF21A | GRCh38.p7 | 11:46116916 | AGGTTGCAGTGAGCC[A/G]AGATCACGCCGTTGC | 51317 |
rs367649230 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46091782 | TGGATGACTTGAATT[A/G]GCTCAAGCCATCCTC | 51317 |
rs367655895 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PHF21A | GRCh38.p7 | 11:45974652 | TAGAGACGTGATCTC[A/G]CTATGTTGCCCAGGC | 51317 |
rs367656241 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45982503 | CTTTCAAGTCTTCAA[A/G]ATTCTATTTCTCCAA | 51317 |
rs367658290 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45947784 | ACCAAGCACAAAACA[A/G]AACAAAACAAAACAA | 51317 |
rs367666888 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45962374 | TTTACCTTTAGCTCT[A/G]TGATCTATGAGATCT | 51317 |
rs367695317 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46071734 | ATATTGATAATAGCC[A/C]AAAAAAAAAACTGGA | 51317 |
rs367705129 | snp | A/G | 0.000115334 | 0.00759299 | synonymous-codon, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45938253 | ACGGGAACATGTGTC[A/G]CACATCAGTAACTGG | 51317 |
rs367708395 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46111028 | GACCTCAGGTGATCC[A/C]CCCGCCTCAGCCTAC | 51317 |
rs367726502 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46100331 | TCATCAGAGCAGCAT[A/G]GGGTCCCATTAGGCA | 51317 |
rs367735966 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45991209 | TTTTTCATGGTTTGA[C/T]AGTTCATTTCTTTTT | 51317 |
rs367743152 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PHF21A | GRCh38.p7 | 11:46026010 | GATTTTGACAATGTC[C/T]CAAGAATGTCCTTTA | 51317 |
rs367748181 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | PHF21A | GRCh38.p7 | 11:45967574 | GGTGGCTTTCCCACT[A/G]TCTTAGATAAGGAGC | 51317 |
rs367774347 | snp | C/T | 1.64741e-05 | 0.00286998 | missense, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45971244 | CCTTCTGACTGTTGA[C/T]GGCGGTCACCATAGC | 51317 |
rs367795112 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45981525 | TAACTATTTGGGGCC[A/G]TATTTGGGCTCTGAC | 51317 |
rs367803872 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45954379 | CATCTCACATACACA[A/G]TCTCCTATTTCGGAA | 51317 |
rs367864982 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | PHF21A | GRCh38.p7 | 11:45955248 | TGGGTGAAGAGTATG[A/G]TCTAAGCGAGAATCA | 51317 |
rs367871548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46115715 | AAATCAGTTCTAGAT[A/G]TAGATATAAAAGAAT | 51317 |
rs367875584 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PHF21A | GRCh38.p7 | 11:45966917 | CCACTGCACCCAGCC[A/G]TAAGCCAGTATTTTT | 51317 |
rs367877824 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46083397 | ACGATTTCAAAAGTT[A/T]ATGTTACCTCAGACT | 51317 |
rs367902723 | in-del | -/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46109030 | AAAATCAACATGAAA[-/C]CAGCCTCAAAATGAT | 51317 |
rs367940260 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46005994 | ATGCCTGTGGAAAAG[C/T]ACAATTTTAAACTTT | 51317 |
rs367959632 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45958199 | TTTAAAGAATTAGCA[C/T]CAATCTGTCTCAAAT | 51317 |
rs368044954 | in-del | -/CTCTCT/CTCTCTCT | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:46121181 | TCTCTCTCTCACTCA[-/CTCTCT/CTCTCTCT]CTCTCTCTCTCTCTC | 51317 |
rs368077380 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46013454 | AAGAGTAGTGATGTA[A/G]TATTTTTGGGCCTCA | 51317 |
rs368086043 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46089655 | GACCTCCTTAGCTAG[C/T]TGGATGTTTCTATAC | 51317 |
rs368112010 | snp | A/C | 0.000316427 | 0.0125743 | intron-variant | PHF21A | GRCh38.p7 | 11:45938318 | GAATATCACCCTATA[A/C]AGTTGAGAGGAAAGG | 51317 |
rs368142853 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46051623 | TCTCATTAACCAGCT[A/G]TTTTTAAGCATGCCA | 51317 |
rs368170466 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | PHF21A | GRCh38.p7 | 11:46001829 | TTTTTAACTAGAGGG[A/G]AGAGGATGGAGGTCT | 51317 |
rs368173029 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45963531 | AAGTTTACTCTCTCT[G/T]TAGATTACGGGGAAA | 51317 |
rs368181546 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46020003 | GACTCTTTTTTTTTT[-/T]AGCCATCATTATGAA | 51317 |
rs368209804 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46026371 | CATGCACAAGGTACA[C/T]GAAAGCTGACAATGA | 51317 |
rs368244343 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45975382 | TAAAATAAAATAAAA[C/T]AAAACAAAATAAAAT | 51317 |
rs368265106 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | PHF21A | GRCh38.p7 | 11:46053197 | TTTCACAGAACACTA[C/G]ATCACATCTCTCATG | 51317 |
rs368269377 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46077950 | GCAGTCTCACTCTGT[C/T]GTCCAGGCTGGAGTG | 51317 |
rs368280159 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46092776 | TTTTTTTTTTTTTTT[G/T]AAACAATGTCTTACT | 51317 |
rs368286058 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45978552 | CAACTGAACTATACT[C/T]TTTTTCTCTCTATAT | 51317 |
rs368286196 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46028332 | AAATAATAATACTAT[A/G]CATCAAAATGTTAAT | 51317 |
rs368312019 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46063351 | TCTCTGGTTAAATTT[A/C]TCTAGAGTAAGATTG | 51317 |
rs368314495 | snp | A/G | 1.72024e-05 | 0.00293273 | intron-variant | PHF21A | GRCh38.p7 | 11:45971083 | TCCTAACCTTCTCAT[A/G]TGATCACACATGAGG | 51317 |
rs368320207 | snp | A/T | | | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46084821 | AGTAGCTGGGACTAC[A/T]GGCACCTGCCACTAC | 51317 |
rs368325596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45967127 | TAATCCCAACAATTC[A/G]GGAGGCTGAGGCTGG | 51317 |
rs368337006 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46008971 | TGGTTCACATTTCAC[-/T]TTTTTTTTTTTTTTT | 51317 |
rs368350444 | snp | A/G | | | synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45935696 | TCGTTCTTGTTTTAA[A/G]TCTGAACTCCATTTA | 51317 |
rs368360578 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45990070 | ATTTTTCACAGGTGA[C/T]GAAAATTACAAAATC | 51317 |
rs368399176 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46003256 | TATAGTGTATGGAGG[A/G]AAGAGCTTGGGTTAA | 51317 |
rs368412505 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PHF21A | GRCh38.p7 | 11:45946502 | CATTCTCCTGCCTCA[A/G]CCTCCCACGTAGCTG | 51317 |
rs368413817 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45995438 | TACCTATACTTCACA[A/G]CATGTTTGTGTGACA | 51317 |
rs368418960 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45989325 | AAGAAAAGCATGAAC[A/G]ATCTCTTAATGAATA | 51317 |
rs368470297 | snp | A/G | 0.00017409 | 0.00932816 | downstream-variant-500B, utr-variant-3-prime, synonymous-codon | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45928858 | TGAGGCTGGGCCGGC[A/G]CTGCCCCTCATCTTA | 51317 |
rs368471718 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46071129 | TTTGTCATATAACTT[C/T]GCAAGGCTTGGCCAT | 51317 |
rs368477730 | snp | C/T | 1.65499e-05 | 0.00287657 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45953583 | GGGTGATGGTGCGGC[C/T]CTCTGTTTGTTTCTC | 51317 |
rs368514544 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45931923 | CCGGCCAAGCCGAGG[C/T]AAGCGCAGCAATTCT | 51317 |
rs368526920 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46020019 | AGCCATCATTATGAA[A/G]AGACCTGAATGATGA | 51317 |
rs368545798 | snp | C/G | 0.000544951 | 0.0164978 | intron-variant | PHF21A | GRCh38.p7 | 11:45935788 | TTTTGACAATTAATT[C/G]TTTGAAATGTCCTCT | 51317 |
rs368556251 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930682 | CACTGCCACCAGGGC[A/G]CAGCGCCTGATCAGG | 51317 |
rs368593404 | snp | A/G | 1.65102e-05 | 0.00287312 | intron-variant | PHF21A | GRCh38.p7 | 11:46079188 | ATAAAGAGAGAAAAA[A/G]AGCCATCAGTCTTAC | 51317 |
rs368638492 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45945514 | TCCCAAAACACTGAT[A/G]ATAGAAACCTGCACA | 51317 |
rs368654402 | in-del | -/AATAAACACACA | | | intron-variant | PHF21A | GRCh38.p7 | 11:46025082 | TAGAAACTTTATGAA[-/AATAAACACACA]CTGCCTATCCACAAG | 51317 |
rs368657307 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | PHF21A | GRCh38.p7 | 11:46070022 | ACATATTAAGTTATT[C/T]AATAATTAAAATCTA | 51317 |
rs368718824 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46034783 | TGTGTAAGAAGTCTT[A/C]CATGACCCAGTTTCC | 51317 |
rs368739447 | snp | C/T | 0.000875616 | 0.0209055 | intron-variant | PHF21A | GRCh38.p7 | 11:45950328 | ATTGCCAGTTCCTAG[C/T]AGGACATTAGGGAAA | 51317 |
rs368743559 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46009464 | CCAAGTGTCTGAACC[A/G]TACAATTTAACATCT | 51317 |
rs368747519 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:46084204 | TAAGAGCCTCCTGTA[A/G]AGTCTGCAACTCCAT | 51317 |
rs368749522 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45964015 | ATCAGCTGACCAACA[C/T]GGAGAAACCCCGTCT | 51317 |
rs368750735 | in-del | -/C | | | splice-acceptor-variant | PHF21A | GRCh38.p7 | 11:45935740 | TCTCTTCTTCTTTTG[-/C]TAAAAAAAAAAAAAA | 51317 |
rs368800413 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46063842 | TCTGATGAACCCACA[A/T]CATAGGATAAGCAGA | 51317 |
rs368816461 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46084860 | CATTTTTTTATATTT[G/T]TAATAGAGACGGGGT | 51317 |
rs368844529 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45984768 | TGCCCTCCACAACTG[G/T]ATGTCAGTGCTGCAA | 51317 |
rs368850022 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46073463 | TAAAAAAATTTTTTA[A/T]ATCTTATTTCTTGTC | 51317 |
rs368886127 | snp | C/T | 1.75647e-05 | 0.00296345 | synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45965525 | CAGCATGACGGGCCT[C/T]TGGATAAGCTGAGGA | 51317 |
rs368897984 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46107888 | AAATACTGAGTTATC[A/C]GCATAGCATTTGGTA | 51317 |
rs368938087 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45987554 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 51317 |
rs368942912 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46058919 | GAAAGTCAATCTCTA[C/G]ACAGCAGAAATGAAG | 51317 |
rs368948693 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PHF21A | GRCh38.p7 | 11:46096109 | GAAAAAGCAGAATCC[C/T]GCTTGATAGGCTTAG | 51317 |
rs368968907 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45970785 | CACTCAAGTTTCACA[A/G]GAAAACACTGTAGAG | 51317 |
rs368970258 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | PHF21A | GRCh38.p7 | 11:46009141 | CACCATGCCCAGCTA[A/C]TTTTCTGTATTTAGT | 51317 |
rs368990908 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46059884 | GGCACCCACCACCAC[A/G]CCCAGCTGATTTTAT | 51317 |
rs368992522 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45997497 | AGCCAGCCCATGCCT[A/G]CGTGAAACAGCTCCT | 51317 |
rs369002359 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46054566 | TTTATTAGGGTACCA[A/G]CTAGGGCTGAGAACC | 51317 |
rs369007930 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45948928 | TGCTGTTTAGGTATG[C/T]CACTGCACTCTTCTT | 51317 |
rs369008041 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45967340 | GCCACTGCACTCCAG[C/T]CTGGGTGATAGAGTG | 51317 |
rs369021883 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46086133 | ACTATCTTTTTTTTT[C/T]TTTGAGAAAGAGTCT | 51317 |
rs369035329 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46038139 | CTCTCTTTTTTTTTT[-/T]AAATGGAGTTTTGCT | 51317 |
rs369043301 | in-del | -/CACC/CC | | | intron-variant | PHF21A | GRCh38.p7 | 11:46099560 | ACACACACACACACA[-/CACC/CC]CACCCTAAACACAAA | 51317 |
rs369045954 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45970892 | TCATACTTTGACCTC[A/T]GATAATGCACTGAAT | 51317 |
rs369074726 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45952214 | GTGATTCTGTCCAAC[A/T]AGAAGGTGAACTATA | 51317 |
rs369093084 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46053560 | ATATGTATACCATGA[C/T]TGGTAAAAAGAACCC | 51317 |
rs369098061 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46021528 | ATTGCACATGTGTGT[A/G]CGTGCATGTGTGTGT | 51317 |
rs369108609 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46014382 | ATATTCCAGTGTATA[G/T]GCACCACATTTTCTT | 51317 |
rs369111295 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46003818 | TGCCCTTCATCAATT[A/G]CTTCCTATGCCAGGA | 51317 |
rs369116906 | snp | A/T | 0.00010812 | 0.00735175 | intron-variant | PHF21A | GRCh38.p7 | 11:45945813 | TAAGCTCTCAGAAAG[A/T]CAGTGTGCTTTTCCC | 51317 |
rs369162529 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46028852 | GCTGGGATTACAGGC[A/G]TGAGCCACCACGCCC | 51317 |
rs369163062 | in-del | -/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45955842 | GGAACCTCCAGCCAA[-/C]CAGCCAGTGAAGAAG | 51317 |
rs369187810 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45979517 | TTTTGTTATTGACTA[C/T]CTTTCTCCCCTTCTT | 51317 |
rs369192032 | in-del | -/AG | 0.216349 | 0.247725 | intron-variant | PHF21A | GRCh38.p7 | 11:46021074 | TTAAAAAAAAAAAAA[-/AG]AGAGAGACAAGGTCT | 51317 |
rs369205260 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46086818 | GAAATGAACGGCAGG[G/T]TAAAACACAAAGAAC | 51317 |
rs369258051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46078250 | TCTCAATTTGTAGAG[A/G]TAAGTGTTATTTTTT | 51317 |
rs369329297 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46029414 | CTTCACTGGCTGGGC[A/G]CAGTGGCTCACGCCT | 51317 |
rs369347099 | snp | A/G | 0.00455331 | 0.0474966 | intron-variant | PHF21A | GRCh38.p7 | 11:45979732 | AGTCTACAATCTGCA[A/G]CCTGCAATGTTCCAT | 51317 |
rs369376668 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46005014 | TATGGAAAATGAGAT[C/T]ATGCAGTTAAATTTT | 51317 |
rs369380826 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45960279 | AGTGGAACCAACCAA[C/T]GTCTTATGATTTCCT | 51317 |
rs369393137 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46079934 | TGTCTTTTGACCTAA[C/T]CCAACTTCTAAAGAC | 51317 |
rs369443440 | snp | C/T | 7.22818e-05 | 0.00601129 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45933953 | GATCCCGTGGCTTCT[C/T]CTAGAGGGGCTCTGT | 51317 |
rs369528221 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46054251 | AAGTCAGAGTATTAA[A/T]ATGATAGTAACCCTT | 51317 |
rs369529275 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46048780 | ATCTCAAAAAAAAAA[A/T]AATTTTTTTTTTGTT | 51317 |
rs369529792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46036248 | GTAAAATTTACAGTC[A/G]TAAGTAACATAACTG | 51317 |
rs369539693 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46104191 | ATGCCACTTTTATAT[A/C]TCTGGGGTTCTACAA | 51317 |
rs369554287 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45992553 | CTCCGTCTCAAAAAA[G/T]AAAATTTTTTGACAT | 51317 |
rs369566250 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant | PHF21A | GRCh38.p7 | 11:46079229 | CCTATGGCTAATCAG[A/G]TTTGGACCAAAAAAT | 51317 |
rs369574483 | snp | A/G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46014747 | GCACTTTGGGAGGCC[A/G/T]AGGCGGGCGGATCAC | 51317 |
rs369596914 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46035031 | AAAGAGTAACTAGTC[C/T]ATGAGGACTGAAGAG | 51317 |
rs369606267 | snp | C/G | 3.29489e-05 | 0.00405874 | intron-variant | PHF21A | GRCh38.p7 | 11:45949485 | TGCTTTGGATTTCTT[C/G]AGAGAAGAAAAGGTT | 51317 |
rs369613756 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45998793 | CTGGGATGCTGGGAT[A/T]ACAGGCATGAGCCAC | 51317 |
rs369624628 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46006586 | CTGTCTGCCTGAGCT[A/G]GAGGATGAAGTTATG | 51317 |
rs369633006 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45964092 | ATCCCAGCTACTCAG[A/G]AGGCTGAGGCAAGGA | 51317 |
rs369648911 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45938689 | GAAAACAGAACAATT[A/G]TAACGATATACTGTA | 51317 |
rs369657229 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46113824 | GTGAGATTCATTCTC[-/A]AAAAAAAAAAAAAAA | 51317 |
rs369688299 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45992527 | CCTGAGCGCTGGGTG[A/T]CAGAGCGAGACTCCG | 51317 |
rs369700401 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46086894 | GGCCCTCAAAAATTG[A/G]TAACAAAAATCTATG | 51317 |
rs369720607 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46022016 | GTGAAGCAGAGATAA[C/T]TAAGCAATATTTTCT | 51317 |
rs369816781 | snp | C/T | | | intron-variant, downstream-variant-500B | PHF21A | GRCh38.p7 | 11:45934819 | TTTTGCCCTTTTGCC[C/T]TCAGCTTCCCACACC | 51317 |
rs369818959 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46019649 | ATGCTTTACTTTTAT[A/G]TTAACTTAAGCAATC | 51317 |
rs369827850 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46103460 | TTTAAAAATATTTGT[C/T]GAGCCAAAGTACACC | 51317 |
rs369839675 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46091993 | CTAGCTGTATTAGCA[C/G]AAACACAAATGCGTT | 51317 |
rs369842313 | in-del | -/TATTT | 0.00279162 | 0.0372561 | intron-variant | PHF21A | GRCh38.p7 | 11:46080150 | CTAAAATATACTATA[-/TATTT]ATCTAACTACTAGTT | 51317 |
rs369847460 | in-del | -/AAAAAAAAAA | 0.0941369 | 0.195465 | intron-variant | PHF21A | GRCh38.p7 | 11:45968932 | GCGAAACTCCATTGC[-/AAAAAAAAAA]AAAAAAAAAAAAAAA | 51317 |
rs369929052 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45991044 | GTCTATTCAGCACAA[C/T]CTTCCCTCACCCTCT | 51317 |
rs369967827 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46020568 | TCTAACACCATCTGA[C/T]GATCTAGAATATAAA | 51317 |
rs369971487 | snp | A/G | 0.000256404 | 0.0113197 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45965340 | AGACTTGGCTTGCTA[A/G]GCTGTACAGTTTGAG | 51317 |
rs369977379 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45951585 | CCAACTAACTACATT[C/T]CTAATTTTCACTATT | 51317 |
rs370006611 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46035734 | GGGAGGAGAACAGTG[C/T]CTCAGAAGGGAGACC | 51317 |
rs370042740 | snp | A/G | | | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46086274 | CAGGTGCCCGCCACT[A/G]CACCCGGCTAATTTT | 51317 |
rs370066255 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46015025 | AAAAAAAAATAAAAA[A/T]ATAAAAAATAGTTAT | 51317 |
rs370086539 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46026051 | AGTCTCAGATCATGC[C/G]AAGTTATCTAAATAT | 51317 |
rs370092547 | snp | C/T | 0.000122182 | 0.00781512 | intron-variant | PHF21A | GRCh38.p7 | 11:45969790 | CCATCTAACCTATCA[C/T]TGAGCTTGTCATTGG | 51317 |
rs370098777 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46021212 | CTACAGGTGCAAGCC[A/G]CTATGCCTGGCTAAT | 51317 |
rs370166935 | snp | A/G | 0.000153988 | 0.00877328 | missense, synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934218 | GTGTTCTTCATTTCC[A/G]TGCATTTCTGCAGCA | 51317 |
rs370200588 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46115431 | AAATAGTATGGCCAC[A/G]TATACACACAAACAT | 51317 |
rs370209813 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46063468 | AAAAGCAGTCAGTCA[C/T]AGAGAATATGTAAAT | 51317 |
rs370218802 | in-del | -/C | 0.0130921 | 0.0798413 | intron-variant | PHF21A | GRCh38.p7 | 11:46105389 | GGCACACAGGACATG[-/C]CCCTGATGATTAGAT | 51317 |
rs370261903 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46001409 | TACTTAGCCAATGCA[C/T]CTGTAGATTCTAATG | 51317 |
rs370313849 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45943109 | AGCTATCATCATCAT[C/T]ATCTTTCTTTCCTTT | 51317 |
rs370379618 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46081549 | GAGGAAATAAATAAG[A/C]CAATTTTTCTATCTG | 51317 |
rs370381204 | in-del | -/CCTAA | | | intron-variant | PHF21A | GRCh38.p7 | 11:46099564 | CACACACACACACAC[-/CCTAA]ACACAAACACAAACA | 51317 |
rs370421778 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46008446 | CTCAGGAAATGGGCA[G/T]CATACATCTCATCTT | 51317 |
rs370430136 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45963380 | AGCTGAGATCCCACC[A/G]TTGCACTCCAGCTTG | 51317 |
rs370478347 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46099239 | ATCCAGAGAAACACA[C/T]GCACACAAAACAAAA | 51317 |
rs370489997 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46049993 | TATTCTATCATATAT[C/T]TCATGTAGTCACCAC | 51317 |
rs370498555 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45967075 | TGCTTATGATAAAAA[C/T]GACCCTTTCCTGGCC | 51317 |
rs370500537 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46013247 | TGAATAGAAAATTCC[A/G]GAAAAAATAATCCAT | 51317 |
rs370521561 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46007405 | TGCAACCTCCACCTC[C/G]CAAGTTCAAGTGATT | 51317 |
rs370531446 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45982713 | CATCAAACATATTAA[C/T]GAACTAGCTAACGTG | 51317 |
rs370531602 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46093070 | CACATCTTACCACTT[C/T]AGATTGTAAACCACA | 51317 |
rs370532961 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46088203 | AAGTTATAAATAACA[A/G]ATCAGTTGCTGCAAA | 51317 |
rs370533546 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PHF21A | GRCh38.p7 | 11:46032000 | AACATGAAAACCACA[A/G]CTTTATTAGCTGATA | 51317 |
rs370571661 | snp | A/T | 0.000270453 | 0.0116255 | intron-variant | PHF21A | GRCh38.p7 | 11:46076856 | CTGTGAGAAAGATAT[A/T]TCATTTGTTAACAGA | 51317 |
rs370571667 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45985428 | AACAAAAACACAGAA[C/T]GCCATTTTATGGACA | 51317 |
rs370609907 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45966198 | ATGTACTGAAGACTC[A/T]CACTTTTACCTCAGA | 51317 |
rs370612753 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45994213 | GGCAACATTTAGACT[A/G]GGTAAAGTGTTGGGC | 51317 |
rs370621699 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45929938 | GCAGAGGGACAGGGG[C/T]GAGGTTCACACAGAG | 51317 |
rs370627435 | snp | C/T | 0.000148352 | 0.00861127 | missense, synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934143 | ATGCCGTGGATGAGG[C/T]GAATCAGCTGTTTTA | 51317 |
rs370632163 | in-del | -/TTTAA | | | intron-variant | PHF21A | GRCh38.p7 | 11:46007718 | ATTTAGTTACATTAA[-/TTTAA]ATCAAAAAACGATGT | 51317 |
rs370685997 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46069794 | TGCACTTGTGATTGA[G/T]TTAAATGTTAAATGT | 51317 |
rs370718662 | snp | C/G | | | upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46122353 | CCCGGCCGCCGCTCG[C/G]CCGCTCCCTCCCCTC | 51317 |
rs370729723 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:46023940 | CATCCTGGGCGACAC[A/G]GCAAGACACCATCTC | 51317 |
rs370836454 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46105455 | GTTAAGAGCCCCCAG[A/C]CCACCTTTCTCCACA | 51317 |
rs370861807 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | PHF21A | GRCh38.p7 | 11:46030715 | CACATTTGCATTCAA[A/G]TATTTTATGTTCCCA | 51317 |
rs370868329 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46005553 | ATAAAACAGGTTATT[C/T]TGACTCCATTAGCAA | 51317 |
rs370872317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46055799 | ATTGAAAATATAATA[C/T]GATCTAAGCCTAAAA | 51317 |
rs370876373 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45994949 | TATTTTCAACCAAAG[G/T]ACGTAAGAATCTAAC | 51317 |
rs370877031 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45972764 | ACTAAAAATACAAAA[A/C]TCAGCCAGGCCTGGT | 51317 |
rs370877032 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46017073 | CCTCCCAGGTTCCAG[C/T]GATTCTCCTGCCTCA | 51317 |
rs370907044 | snp | A/G | 1.6966e-05 | 0.00291251 | intron-variant | PHF21A | GRCh38.p7 | 11:45934242 | TGCAGCAAATGACAA[A/G]GGCAGTGGCACTGAG | 51317 |
rs370921832 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46033334 | CAGTGGTGCAATCAT[C/G]GCTCACTGCAGCCTC | 51317 |
rs370964585 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46091054 | AAAGGCAAGTAGAAT[-/A]AAAAGGTAGTAAATG | 51317 |
rs370966395 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46043740 | AACATTCCATCCTGA[A/C]TGCAATGTCTGCATC | 51317 |
rs371059162 | snp | A/C | 1.70886e-05 | 0.00292301 | intron-variant | PHF21A | GRCh38.p7 | 11:45971090 | CTTCTCATGTGATCA[A/C]ACATGAGGAGCAGCT | 51317 |
rs371126612 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45979417 | CCAGAAGAGGTCAAG[A/T]CACAAACTTTTAGAA | 51317 |
rs371144813 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45935303 | AGTGTCAGGTGAGGC[A/G]CTACACTCCCCCCAC | 51317 |
rs371197688 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45987237 | GGCAACAGAGCGAGA[C/T]TGTATCATAAATAAA | 51317 |
rs371203874 | snp | C/G/T | 0.000121654 | 0.00779832 | intron-variant | PHF21A | GRCh38.p7 | 11:45953492 | ATAAACCATACACCA[C/G/T]AGACTGAGACCTGCC | 51317 |
rs371211882 | snp | A/T | 1.64746e-05 | 0.00287002 | intron-variant | PHF21A | GRCh38.p7 | 11:45949367 | ATAAATAAAACTGGA[A/T]CATGAGGGAAGGGCC | 51317 |
rs371213531 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46116263 | TCTAAAATAGAAAAA[A/C]AAAAATGATATATCC | 51317 |
rs371232600 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46070174 | AACTAGTTATAGGAG[A/G]GACAGAAACTTCTTT | 51317 |
rs371265768 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46116927 | AGCCGAGATCACGCC[A/G]TTGCACTCCAGCCTG | 51317 |
rs371302419 | snp | A/G | 0.000153988 | 0.00877328 | missense, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45971279 | GTAGGTCTCTGGCCC[A/G]CCACAGAGGCAGGCA | 51317 |
rs371310181 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45991115 | TTTCCAGAATGTCAT[A/G]GAGTTGGAGTCATAC | 51317 |
rs371327409 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46074541 | GGAGTCTTGCTCTGT[C/T]GCCCAGGCTGGAGTG | 51317 |
rs371372891 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45976431 | TGCACACAGTAGGAA[C/G]TCCACAAATATTTAC | 51317 |
rs371380766 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46001094 | AACATATCTTAACCA[C/T]AAAATCAGACATTTT | 51317 |
rs371399534 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46022489 | AACAAAAAGACAGGG[A/T]CTCCCTTTGTCACCT | 51317 |
rs371422108 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46046041 | ATCTTCAGAAATGCA[A/G]TTCTCAGCTTTGTGA | 51317 |
rs371447807 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46039243 | TGTTTTCGTGCATTC[A/G]CTGTTTTAGTATAGG | 51317 |
rs371455070 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46014295 | CTGCATTAATTCCCT[G/T]AGGATAATGGCCTCC | 51317 |
rs371467875 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46082415 | ATCAACAATCGTGTA[A/G]GTGACACCATATAAA | 51317 |
rs371476255 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45991636 | TAGAGAGGCAGTATT[G/T]TGCTGTAAAAATAAT | 51317 |
rs371518017 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46023146 | ACAATTAGAAAAAAA[-/A]GAGAGGAAAAGTTAA | 51317 |
rs371576180 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46052825 | TTCTTGGACATCTCT[A/G]ACCAAGCCATCTTAC | 51317 |
rs371592042 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46002529 | ACTATTTGGGGGAAA[A/G]AAAAAGGAATTCACA | 51317 |
rs371597267 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46012206 | CATCTATCCATTTCC[C/T]TCAGAAAGTATTCAA | 51317 |
rs371599704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45978157 | ATACAAAAATTAGCC[A/G]GGCATGGTGGCACGC | 51317 |
rs371604835 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46026765 | TCTAACGTGCACAGA[C/T]AGCCAAAAGGTACTG | 51317 |
rs371610672 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45955752 | AGGGTGTCTTTCCTT[A/C]GTGGATCTCTTGCTC | 51317 |
rs371624294 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45957816 | AAATGAAATAGAGAA[C/G]AACAACAGACTCAAC | 51317 |
rs371625119 | snp | A/G/T | 4.94501e-05 | 0.00497223 | missense, synonymous-codon, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45938214 | TGTTTTCAGAGGGGG[A/G/T]TCTAAGCAGTCCAAA | 51317 |
rs371629369 | snp | C/T | 1.6528e-05 | 0.00287467 | missense, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45945953 | TGGATTGGGGGGATG[C/T]TGGGGTAAGGGCTCC | 51317 |
rs371635524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46065607 | AAACTACAGCTAAAA[A/G]CATCTGTACTGATAC | 51317 |
rs371651231 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46014756 | GAGGCCGAGGCGGGC[G/T]GATCACGAGGTCAGG | 51317 |
rs371670725 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45968415 | TCTAGCCTGCATGAG[C/T]CACATGGCCCTCTGT | 51317 |
rs371677855 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46086775 | AGTAACATAAAACCA[C/T]AGTTCAATTCAATTC | 51317 |
rs371707698 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:45934549 | AAACAAAGGTTGTTT[-/A]AAAAAAAAAAAAAAG | 51317 |
rs371713739 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45975832 | TATGCCAATCACCCG[A/G]CTTAGAATAAAAAAC | 51317 |
rs371771370 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46046791 | AAGCCTGCCTTCACT[C/T]TGTGAAGAGTGTCTG | 51317 |
rs371783717 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46034964 | CATTCTCTGCCACAC[A/T]GAGTTAGCCTACCGT | 51317 |
rs371795100 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46084516 | CAAAAAAAGGGTTTA[A/G]TCTGGTCATGGAAAC | 51317 |
rs371796490 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45950008 | GGGAGGTTTTCCCAG[G/T]ACAGTAGTGTGGATA | 51317 |
rs371802787 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45975322 | CTGTCTCAAAGAAAA[C/T]AAAATAAAATAAAAT | 51317 |
rs371834902 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46091150 | AGACACCACAAGCAC[C/T]ATAAACTATCAAAAG | 51317 |
rs371839102 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46111330 | TAACAATTAGCCAGG[C/T]ATGGAGGTGCATGCC | 51317 |
rs371895408 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46041338 | ATTTAGGATGTTCAA[G/T]GAAATTACTATGTCA | 51317 |
rs371902130 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45998391 | CAATATTAAATGAAT[A/G]TGCCTACTGAGTATA | 51317 |
rs371902663 | snp | C/T | 1.65187e-05 | 0.00287386 | intron-variant | PHF21A | GRCh38.p7 | 11:46079214 | CTTACATATTAACTC[C/T]CTATGGCTAATCAGG | 51317 |
rs371914854 | in-del | -/T/TT | 0.204496 | 0.245824 | intron-variant | PHF21A | GRCh38.p7 | 11:45951807 | CTCTTGTGGAATAAA[-/T/TT]TTTTTTTTTTTTTTT | 51317 |
rs371928393 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45995253 | CCACTTTTGCCACTA[A/G]TCATAGGGGAGAAAG | 51317 |
rs371930578 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45941311 | CCCTTTATTACCCAG[-/G]CTGGTAAAAACTTTC | 51317 |
rs371948562 | snp | A/G | 3.31389e-05 | 0.00407042 | missense, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45945892 | ACAGGTGCAGGGAAA[A/G]TGAATGTGGTCTCTG | 51317 |
rs372019328 | in-del | -/GTGT | | | intron-variant | PHF21A | GRCh38.p7 | 11:46021556 | TGTGCATGTGTGTGT[-/GTGT]TCAGAGACAGGGTCT | 51317 |
rs372037631 | snp | A/G | 9.90197e-05 | 0.00703563 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45979805 | AGCTGACTGCTGGGC[A/G]TGGTGGTGGTGGTAC | 51317 |
rs372053712 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46040256 | ATAATGGTCTCACCT[C/G]AGTGGAAAAGAGAGG | 51317 |
rs372061206 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46107020 | TCCAGCTGTCCCCAC[A/G]GCTGCCTCTTCTGCA | 51317 |
rs372073213 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46084004 | TCTTAAAAGCAGTAT[C/G]TATGACTTTGTCGAG | 51317 |
rs372078936 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45989158 | ATGTGATAAAGGATA[A/C]TTTGCACTTCTCTGT | 51317 |
rs372101919 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46020416 | TCGATGGGTCTTTGC[A/G/T]CAGCAGCAGGAGGGA | 51317 |
rs372103482 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:46096928 | CCTCAGAGTCATTCC[C/T]ATCTCAGTAAATGGT | 51317 |
rs372110559 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46117876 | CAAAGACTTCACTTT[C/G]AAGTAGCAAACATTA | 51317 |
rs372115450 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46059374 | GAAATGCTCAAGATA[C/T]AGACAAAATAAGTAT | 51317 |
rs372120817 | snp | G/T | 1.78595e-05 | 0.00298822 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45965539 | TCTGGATAAGCTGAG[G/T]AGCTGCGAGCATGGG | 51317 |
rs372141991 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45974166 | AGGCACAAGACCTAG[C/T]ACTGTATGCTTCAGT | 51317 |
rs372156698 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46070534 | CAGGGTTTCGCCATG[C/T]TGGCCAGGCTGGTCT | 51317 |
rs372165215 | in-del | -/CTA | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:46058153 | ACACCTCCCTACATT[-/CTA]CTGCTGCCTTACCAT | 51317 |
rs372169222 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46018958 | CATACCGTAAGCAGC[A/C]AGAACACACACATCA | 51317 |
rs372191623 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45974689 | AGAACTCGCTCTCAC[A/G]TAATCCTCCCACATC | 51317 |
rs372203435 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45958810 | ATAGTCCTAGTTACT[G/T]GGGAGGCTGAAATGG | 51317 |
rs372225934 | in-del | -/A/TA | 0.39536 | 0.203397 | splice-acceptor-variant | PHF21A | GRCh38.p7 | 11:45935741 | TCTTCTTCTTTTGCT[-/A/TA]AAAAAAAAAAAAAAA | 51317 |
rs372240747 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46059407 | CTAAAATAATAAGTA[C/T]AATACCAATCTCAAT | 51317 |
rs372245110 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46026241 | TGACTAAGTTTTAAA[A/G]TTAAAATTCCACCCC | 51317 |
rs372256396 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46058965 | ATGAAGAGACACAAG[A/T]GACAGAGACTCCAGT | 51317 |
rs372273429 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46009424 | GACTCTACCTGCCTA[A/G]AATGATCTGTGAAAC | 51317 |
rs372279969 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46078000 | CACTGCAACCTCTGC[A/C]TCCCAGGTTCAAGTG | 51317 |
rs372287878 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46047156 | GGACCCAGTCTGAGA[G/T]AAAGGCTTCAGGCAG | 51317 |
rs372293640 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46028556 | AAAATATTACTTTAT[A/G]CTTTAAAAGCTTGCC | 51317 |
rs372315125 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46008180 | ATTTGTTTACTCACA[C/T]ACGCCCATACACTCT | 51317 |
rs372351634 | snp | A/T | 0.000307953 | 0.0124049 | intron-variant | PHF21A | GRCh38.p7 | 11:45953668 | CAGAATTCGTTTTTT[A/T]TTAAAAGGATGAAGC | 51317 |
rs372360418 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46038761 | TTCTCTTCCTTTTCT[C/T]ATAAAACCACTAGTT | 51317 |
rs372455906 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45943488 | GCCTGCCCATCATCA[C/T]CTCTTGCCTGGACAA | 51317 |
rs372471352 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45979659 | ACTTTTGTTTAGTTC[C/T]AGCTGAGCTTAGTAT | 51317 |
rs372486510 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45975387 | TAAAATAAAACAAAA[C/T]AAAATAAAATAAAAC | 51317 |
rs372531905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46116276 | AACAAAAATGATATA[C/T]CCATATATACCTAAT | 51317 |
rs372583940 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46008160 | CACCTTCCCCTACAA[C/T]GTGTATTTGTTTACT | 51317 |
rs372617550 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46114293 | ATACAGTTGCTACAC[A/C]CCCTCCTATTTTCTG | 51317 |
rs372644822 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46092005 | GCAGAAACACAAATG[C/T]GTTTGAAGTATAGCT | 51317 |
rs372660566 | snp | C/G/T | 0.00398731 | 0.0445001 | intron-variant | PHF21A | GRCh38.p7 | 11:45989407 | TGCCTATAATCCCAG[C/G/T]ACTTTGGGAGGCCGA | 51317 |
rs372668531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45971736 | TTGCTGTCAATTAAT[C/T]TAAACTTTGTACTAG | 51317 |
rs372688832 | snp | C/G | 0.000131981 | 0.00812237 | intron-variant | PHF21A | GRCh38.p7 | 11:46076740 | AAATATGCCCCCCTC[C/G]CCTTTTCCCCTACCT | 51317 |
rs372697888 | in-del | -/AAG | | | intron-variant | PHF21A | GRCh38.p7 | 11:45955009 | ATGATTACATAAAGA[-/AAG]CGTAAGCATCTGCCT | 51317 |
rs372719754 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46031124 | GCCACCCAAGCTCAA[A/T]GCCTCAGAGTCACTT | 51317 |
rs372727495 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | PHF21A | GRCh38.p7 | 11:45974001 | CACCTGAATTATATA[C/T]TTACCATTAACCCAA | 51317 |
rs372736162 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45931973 | GGCTTGTGGGTGGGT[A/G]GAGTGGAGTAAATTT | 51317 |
rs372738577 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45995458 | TTTGTGTGACAGTTA[C/T]ACTGTCATAATTTTA | 51317 |
rs372741151 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46085441 | AATTTAAATTATTTC[A/G]ATGGCTAATTTATCC | 51317 |
rs372760074 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46032531 | TAATGAACATCCTTA[A/T]AAATGTATCTTTATT | 51317 |
rs372765921 | in-del | -/CTTA | | | intron-variant | PHF21A | GRCh38.p7 | 11:46027328 | TCTGCCATCGTTTAC[-/CTTA]TTTATACATGTATAA | 51317 |
rs372774959 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46015026 | AAAAAAAATAAAAAA[A/T]TAAAAAATAGTTATT | 51317 |
rs372785569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45946836 | ATGAGGGTGGAGACC[A/G]GCAAAGCAAGGAGGC | 51317 |
rs372785710 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46104238 | TTACACCCAAGCATG[A/G]GTTCTCAAGGGTTAA | 51317 |
rs372818813 | snp | A/T | 1.88831e-05 | 0.00307265 | intron-variant | PHF21A | GRCh38.p7 | 11:45946132 | TGAGGTAGCAGACAG[A/T]AGGTTAATTCAACAG | 51317 |
rs372848607 | snp | A/T | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:46121110 | CTTTTTAGATATTAG[A/T]GTGTTAAGATGGTAG | 51317 |
rs372850156 | snp | C/G | 4.95446e-05 | 0.00497693 | intron-variant | PHF21A | GRCh38.p7 | 11:45936585 | CTGAAAAGATTTTTA[C/G]AATTTTACCTTGAGA | 51317 |
rs372853435 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45967229 | GAACATTAGCCAGGC[A/T]TGGTGGCACACACTT | 51317 |
rs372866292 | snp | A/C/T | 0.000148873 | 0.00862648 | intron-variant | PHF21A | GRCh38.p7 | 11:46076719 | ATCTTTAGAACACAA[A/C/T]GTTAAAAATATGCCC | 51317 |
rs372880875 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45937641 | GCCTGCCACCATGCC[C/T]GGCTAATTTTTATAT | 51317 |
rs372883088 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | PHF21A | GRCh38.p7 | 11:45949215 | TCTGCTGAAACTTAG[-/A]GAAAAAAACCTAAGG | 51317 |
rs372890358 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46010074 | CTTAACCATATCATA[C/T]TAAAAGAAAGGGGAG | 51317 |
rs372903695 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45977433 | TGTGCCACTGTGCCT[A/G]GCCTCCTTTGATTTT | 51317 |
rs372917577 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45999906 | GTGGTGAACAGGAAG[A/G]CTTGTCTTATCCTCT | 51317 |
rs372929348 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45952521 | CTCAGAGCATAATAC[C/T]TGTCATTAATTCTGT | 51317 |
rs372945539 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:45958305 | AGAAAATGGGCTGGG[C/T]GTGGTGGCTCACTTT | 51317 |
rs372948747 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46004632 | TCTTATCAAACAAAA[A/G]CTCACTTTTCTTCAT | 51317 |
rs372978240 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45946184 | CAAAGATTTAAATGT[C/G]ATTAGAAACAACTAT | 51317 |
rs372985613 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46113552 | TTAATTGTTTTGGCC[A/G]GGCGCGGTGGCTCAC | 51317 |
rs373010140 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45985465 | CAGAAGAGAAACTCA[A/G]GATAAACTCCCTCCT | 51317 |
rs373013037 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45986456 | GAGATGTGACCCCTA[C/G]AGAATTACAGATTCT | 51317 |
rs373014908 | snp | C/T | | | intron-variant, downstream-variant-500B | PHF21A | GRCh38.p7 | 11:45935091 | CAACCCTCTTTCCCA[C/T]TTGGACAGGCCGGGC | 51317 |
rs373094874 | in-del | -/AAAAAAAAAAAAA | | | intron-variant | PHF21A | GRCh38.p7 | 11:45968945 | GCAAAAAAAAAAAAA[-/AAAAAAAAAAAAA]TAGGCAGGTATCCCT | 51317 |
rs373186108 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46103596 | ACACCTATTCACCTA[C/T]TAGACCTTTATCAAA | 51317 |
rs373217561 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46024376 | TTTCTGCTTGTTATT[-/A]AGCAACATCACTTTT | 51317 |
rs373246171 | snp | A/G | | | upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46122656 | TTTTATGCCTATTCT[A/G]CCTCCAAGGACTGTA | 51317 |
rs373259563 | snp | A/C | | | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46084825 | GCTGGGACTACAGGC[A/C]CCTGCCACTACGCCC | 51317 |
rs373263569 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PHF21A | GRCh38.p7 | 11:46074222 | TTTTCTAATAAATAT[C/T]GAAAAAAATGATTAC | 51317 |
rs373268719 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46087157 | TTGATATTTTCAAAA[C/T]TTTCCATAAAAAATA | 51317 |
rs373311808 | in-del | -/GAGA | | | intron-variant | PHF21A | GRCh38.p7 | 11:45996523 | AGACAGAGAGAGAGA[-/GAGA]AACGTATTCCATTAA | 51317 |
rs373332045 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45939845 | GCCTAGCTCATTCTC[A/T]GGATGGGATTAAATC | 51317 |
rs373348305 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PHF21A | GRCh38.p7 | 11:46061214 | GTCACTGTGACCCTG[C/T]AGTATAGTTTGAAGT | 51317 |
rs373358744 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45961679 | GGGTGGCAGTGGGGT[A/G]GAGAAGAAACATAAT | 51317 |
rs373361755 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46048104 | CATTGCCACTGCCCC[A/G]AAAAGGAACTCTGTG | 51317 |
rs373380528 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PHF21A | GRCh38.p7 | 11:45966324 | AATCTTCTCTTCCTC[C/T]GATAATTGCCTCAGT | 51317 |
rs373392576 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46021120 | GTGGGAGTGCAGTGG[C/T]AGGATCATAGCTCAC | 51317 |
rs373397587 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45987285 | GTATGTATGTATGTA[A/T]CCTGACCCATCAAAG | 51317 |
rs373398246 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45975575 | AAAGGTTTGTTTTCC[A/C]TTTGGTTTTATTAAC | 51317 |
rs373408515 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:45981393 | GTGAAACCCTGTCTC[-/A]AAAAAAAAAAAAAAA | 51317 |
rs373411765 | snp | C/T | 0.000155233 | 0.00880864 | intron-variant | PHF21A | GRCh38.p7 | 11:45934259 | GCAGTGGCACTGAGC[C/T]GCCTGGTTTCTAACA | 51317 |
rs373430160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45984384 | ATTCCCTTGACATTC[A/G]CATCACTGGGTTTCA | 51317 |
rs373473917 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45961419 | TATTTTCTCTACTAT[C/T]GCACCAGTATTAAAA | 51317 |
rs373476834 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46063499 | GTAAAGAGTGTGATT[G/T]TGTTCTAATAATTTT | 51317 |
rs373489676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45992779 | ATATACAAAATATAA[C/T]AGTGGAAATGAAAAT | 51317 |
rs373490461 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45964272 | AAGCACTTCCTGGGG[C/T]TTGAATAGGTTCCCC | 51317 |
rs373505398 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45969753 | ACAGGCTACTTAGAA[A/G]GAGCCCATGAGGATT | 51317 |
rs373514109 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45941251 | CTACAAGTGCGTACC[A/G]CCATGCCCGGCTAAT | 51317 |
rs373530483 | snp | C/T | 4.94376e-05 | 0.00497156 | intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45946038 | AACAAAAGGGAAAAA[C/T]GGGGAGGGAAAGAGA | 51317 |
rs373608817 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | PHF21A | GRCh38.p7 | 11:46073315 | CCTGGGCAACAAAGC[A/G]AGACCCCGTCTCAAA | 51317 |
rs373632652 | snp | A/C | 3.42777e-05 | 0.00413977 | downstream-variant-500B, missense, utr-variant-3-prime | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45928823 | CAGCCCTGCAGCAGC[A/C]CCAGAGCCCTGCCCG | 51317 |
rs373638104 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46055512 | AGACTTTGCTCTCCA[C/T]AGAGCTTTTACTGTT | 51317 |
rs373664975 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46005028 | TTATGCAGTTAAATT[C/T]TAACACATGCATGTA | 51317 |
rs373758304 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | PHF21A | GRCh38.p7 | 11:46011382 | TAATCCCAGGTACTT[A/C]GGAGGCTGAGGCAGG | 51317 |
rs373760013 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46054735 | AAGAGAAGCTTTTTC[A/C]GCCTTGTTCATCACT | 51317 |
rs373761230 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45972730 | ACCAGCCTGGCCAAC[A/G]TGGTGAAACCCCATC | 51317 |
rs373767892 | snp | A/G | 1.65051e-05 | 0.00287267 | missense, synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934119 | GAGTCTACAGGTTTG[A/G]AGAGGTCGATGCCGT | 51317 |
rs373807447 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46031755 | ATAGTGTCTGGAAAA[G/T]AATGCAATAATTTTT | 51317 |
rs373829450 | snp | A/T | 0.000153988 | 0.00877328 | intron-variant | PHF21A | GRCh38.p7 | 11:46079187 | AATAAAGAGAGAAAA[A/T]GAGCCATCAGTCTTA | 51317 |
rs373842915 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46009931 | ACAGATAAAGGGGCC[A/G]TCAGTCACTTTACAG | 51317 |
rs373855533 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45953559 | GTTTTGGTTTGGGTG[C/T]AGCAGGTGGGGTGAT | 51317 |
rs373895637 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45933700 | AGAGAGAGTAAATAT[A/G]TTATTTCACTTGGCA | 51317 |
rs373913532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46017979 | TCCTAGGCCGGGCGC[A/G]GTGGCTCACGCCTGT | 51317 |
rs373915657 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45972769 | AAATACAAAAATCAG[C/T]CAGGCCTGGTGGCAG | 51317 |
rs373917182 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46058256 | CCAATCATTTACTTA[C/G]AAAAAAATGAATGGT | 51317 |
rs373917512 | snp | G/T | 1.64817e-05 | 0.00287064 | missense, utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45979830 | TGGTACTGCTGCTGT[G/T]GTTGTAGTTGCTGTA | 51317 |
rs373924016 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46105625 | CACCATAAAAAAAAA[A/C]ACAAAAGGAATGAAT | 51317 |
rs373930757 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45969761 | CTTAGAAAGAGCCCA[C/T]GAGGATTTCTGTCCC | 51317 |
rs373937785 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | PHF21A | GRCh38.p7 | 11:46032160 | CCTTAGTTAGGATCA[A/C]CCTGCTACACAAAAT | 51317 |
rs374017792 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PHF21A | GRCh38.p7 | 11:46062664 | TTGGCTATGTTCATA[C/T]TTAAGATTGAAGCGC | 51317 |
rs374028720 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46088455 | CATAAAAACCAAACA[C/T]ACAAACCAAACACAC | 51317 |
rs374041035 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:46037543 | CTACTTGGGAGGCTG[A/G]GGCAGGACAATCGCT | 51317 |
rs374043812 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45989472 | AACCTGGCTAACACG[A/G]TGAAACCCCATCTCT | 51317 |
rs374045572 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46012356 | CTTCTTAGACCCTTT[C/T]ATATTCAGATGCTTT | 51317 |
rs374073550 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46117567 | TCCGAGGGGAAAAAA[-/A]CTACAAGAAGTCTAA | 51317 |
rs374137701 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930491 | GGCCTGATAAGGAAG[A/G]AAGAAATCAAAACCC | 51317 |
rs374147814 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46064526 | ACTTTGGGAAACATA[C/T]CTTCTGAAAACATAA | 51317 |
rs374156740 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45974090 | TTTATTTTACAACTA[C/T]GGTTATGGCTGATTT | 51317 |
rs374227904 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46036364 | TGGGCAGCTGGGCTA[G/T]AAATGTAACATTCTC | 51317 |
rs374261564 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46058787 | ATTCTCTTTACAAAA[C/T]CTGGAACAAGAACAA | 51317 |
rs374279867 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46084618 | CACTTCTGTCTTCAA[C/T]GAGACTATAACCATC | 51317 |
rs374384809 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46089585 | CCTGATTTTCGAGGC[A/G]AACCCTCTGAATGTG | 51317 |
rs374415498 | snp | A/G | 6.95725e-05 | 0.00589758 | synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45965519 | CTTGGTCAGCATGAC[A/G]GGCCTCTGGATAAGC | 51317 |
rs374419930 | snp | C/T | 3.43083e-05 | 0.00414161 | intron-variant | PHF21A | GRCh38.p7 | 11:45969802 | TCATTGAGCTTGTCA[C/T]TGGTTTACTCACCTG | 51317 |
rs374421429 | snp | A/G/T | 0.00170267 | 0.0291291 | intron-variant | PHF21A | GRCh38.p7 | 11:45971065 | ATACTATACAAATGC[A/G/T]TATCCTAACCTTCTC | 51317 |
rs374426147 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46025127 | CTTTCTCTGAAAGAG[A/G]TAACAGTGACAGGAA | 51317 |
rs374432074 | snp | A/G | 1.6966e-05 | 0.00291251 | intron-variant | PHF21A | GRCh38.p7 | 11:45971095 | CATGTGATCACACAT[A/G]AGGAGCAGCTGCTGG | 51317 |
rs374459075 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46056968 | AGCTTAAAGATAACT[G/T]ATTTTATTTGCTTTA | 51317 |
rs374478762 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45974073 | TAGGTTAGCAGTTTT[A/C]TTTTATTTTACAACT | 51317 |
rs374481302 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46007072 | CATTACAAAAACACT[G/T]AAATATAGAGTGACT | 51317 |
rs374485340 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46100204 | TTGATATTAATGCTA[G/T]CCTTTAAGACCAAAA | 51317 |
rs374507344 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46056210 | TTTTTTTAAGTTAGA[C/T]AGCAATTTAGCAATT | 51317 |
rs374553564 | snp | G/T | 3.41058e-05 | 0.00412938 | missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934023 | CTCTGGGAGGAGGGG[G/T]AAGGGGCCGGCGTGG | 51317 |
rs374562531 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45970465 | GCCATTTTAAGGGAA[G/T]TTTACATCAAAATTT | 51317 |
rs374563798 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45957770 | AAAAAAAAAAAAAAA[-/G]AAAAAAGAAAATAAA | 51317 |
rs374564197 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45974228 | ATTGACACCAAGACC[A/C]AGGTAGTGCTTAGAT | 51317 |
rs374565849 | snp | C/T | 9.21893e-05 | 0.00678868 | intron-variant | PHF21A | GRCh38.p7 | 11:45965272 | AGCCATATGCCTCAA[C/T]GACAAGGCTACTGCC | 51317 |
rs374568278 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45931796 | AGGGGCACGCAAGGG[C/G]CAAAGGTCTCCAGCG | 51317 |
rs374586100 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934144 | TGCCGTGGATGAGGC[A/G]AATCAGCTGTTTTAC | 51317 |
rs374612816 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46043436 | TGGTTAACATACTAC[C/T]TTCTATATCTAGAAA | 51317 |
rs374662224 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45944447 | TTTCAAAATAAATAC[C/T]GAAAAATTATGTCAC | 51317 |
rs374696601 | in-del | -/TT | | | intron-variant | PHF21A | GRCh38.p7 | 11:45940656 | TTTCTTCCTTCATTA[-/TT]TTAAAATCAGGCTGA | 51317 |
rs374699916 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45963033 | CGACAGGAAAAGATG[C/T]TTAAGATCTATTAAA | 51317 |
rs374733403 | snp | C/G/T | 0.000627925 | 0.0177081 | downstream-variant-500B, utr-variant-3-prime, missense | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45928854 | AGGCTGAGGCTGGGC[C/G/T]GGCGCTGCCCCTCAT | 51317 |
rs374764283 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45991370 | TTACTTGCCAGGTAG[A/T]ACAATGAGGCTCTGA | 51317 |
rs374768210 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46021491 | ACCAAGGGTGCCACA[A/G]AAAGCAATCAAAGAG | 51317 |
rs374773338 | snp | A/C | | | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46120218 | CCAGATCCCTCAGTC[A/C]ACAAACAAGATGGTT | 51317 |
rs374786118 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46098509 | AGCAGAAATAAATAG[A/G]AAGAAGAAATCTTGC | 51317 |
rs374787647 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46073389 | ATTTAATACCATGAG[A/G]AGAATGTCATTAGAT | 51317 |
rs374820378 | snp | C/T | 0.000294367 | 0.0121284 | intron-variant | PHF21A | GRCh38.p7 | 11:45935769 | AAAAAAAAAAAGGAA[C/T]GGTTTTTGACAATTA | 51317 |
rs374841336 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45963439 | AAAAAAAAAAAAAAA[-/G]AAAAGAAAAAAAAAT | 51317 |
rs374916339 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46055048 | ATCTACAGGTTAGAG[C/T]GCCAAAACGTCTTTC | 51317 |
rs374935586 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46092910 | CTTCAAGTGTGCCAC[C/T]ATGCCTGGCTATTAC | 51317 |
rs374945142 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46096545 | TTGACCCACTGCTCA[C/T]TTCTTCCTCCTCAAA | 51317 |
rs375030687 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45956792 | TATACAGAAAACAAA[C/T]AGCAAAATGGCGTAA | 51317 |
rs375036326 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45987931 | CTCCCATTCCTCTGC[A/T]CTGTAGCTGCTGTGG | 51317 |
rs375040302 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46086125 | TTTTAGCTACTATCT[A/T]TTTTTTTTTTTGAGA | 51317 |
rs375044805 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45974620 | TACCACACCTGGCTA[A/T]TTTTTTTTATTTTTA | 51317 |
rs375074054 | in-del | -/TA | | | intron-variant | PHF21A | GRCh38.p7 | 11:46108568 | AAATGTGTGTGTGTG[-/TA]TATATATATATATAT | 51317 |
rs375091067 | in-del | -/A | 0.436692 | 0.166271 | intron-variant | PHF21A | GRCh38.p7 | 11:45992376 | CTATACTAAAAATAC[-/A]AAAAAAAAAAAAAAT | 51317 |
rs375136947 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46071107 | TTAAAATTATACATT[C/T]ACACCCTTTGTCATA | 51317 |
rs375145030 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46072670 | TGAGATAATAATAGA[A/G]ACAGTTGATTTTGAC | 51317 |
rs375146676 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:46047364 | CCTTGATGGTTTATC[A/G]TGAAGCATTTTTATA | 51317 |
rs375165976 | snp | C/T | | | upstream-variant-2KB | PHF21A, LOC105376661 | GRCh38.p7 | 11:46123154 | GCAACAGTGGTGAGA[C/T]GATTTGCCCAAAGTC | 51317 |
rs375167458 | snp | A/G | | | intron-variant, downstream-variant-500B | PHF21A | GRCh38.p7 | 11:45934715 | AGCAGGAAGTGAGAC[A/G]ACAGGCCAGCAGCAT | 51317 |
rs375180158 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45974704 | GTAATCCTCCCACAT[C/T]GGCCTCCCAAAGTGT | 51317 |
rs375203423 | snp | G/T | | | intron-variant, utr-variant-5-prime | PHF21A | GRCh38.p7 | 11:46088581 | TCACTGTGTGACTAC[G/T]CTCATCCCCAGGGTT | 51317 |
rs375227546 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46053123 | TTTTCAATTCAAAAT[G/T]TGTAATTAAATGTAA | 51317 |
rs375246425 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46060383 | AATATTCTAGTCTCC[G/T]CCTACAGCTCTAAGA | 51317 |
rs375260855 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45968032 | GACTAAACCTTAGAT[C/T]CCTTACCCTAAAAAG | 51317 |
rs375262339 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45938083 | GACTGCCATTTCCCC[A/C/G]GGAAAGGAATTCCTC | 51317 |
rs375277440 | snp | C/G | 3.29506e-05 | 0.00405884 | intron-variant | PHF21A | GRCh38.p7 | 11:45948842 | AAACACACACACAAA[C/G]CAAAAGCAACAGCAG | 51317 |
rs375277864 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45945336 | GTATTTGACAGTTTT[C/T]CCGGAACCTGTTTCT | 51317 |
rs375291032 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46054025 | CGCCACAAGCTTTTT[C/T]ACAAGCAACGTCGTG | 51317 |
rs375318501 | snp | A/G | 5.05983e-05 | 0.00502957 | intron-variant | PHF21A | GRCh38.p7 | 11:45938328 | CTATAAAGTTGAGAG[A/G]AAAGGTAAGAAAAAG | 51317 |
rs375353258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45967126 | GTAATCCCAACAATT[C/T]GGGAGGCTGAGGCTG | 51317 |
rs375367359 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45946008 | TGGAGGACGACCTAT[A/G]TACCAAGAGAAGGGA | 51317 |
rs375369650 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45995427 | ACAGGGGTGCATACC[C/T]ATACTTCACAGCATG | 51317 |
rs375439396 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46001356 | CACTAGATATCACTG[C/T]TATCAACAAATTTCT | 51317 |
rs375462362 | in-del | -/GC | 9.25134e-05 | 0.0068006 | splice-acceptor-variant | PHF21A | GRCh38.p7 | 11:45935739 | TTCTCTTCTTCTTTT[-/GC]TAAAAAAAAAAAAAA | 51317 |
rs375466721 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46080955 | AGGCGTAAGCCACCA[C/T]GCGCAGCTCTTGCTA | 51317 |
rs375495711 | snp | A/C/T | 3.30246e-05 | 0.0040634 | missense, synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934191 | TGCATCTCCTTCTGC[A/C/T]GGGCCAGGATGGTGT | 51317 |
rs375497452 | snp | A/C/G | 9.01091e-05 | 0.00671175 | intron-variant | PHF21A | GRCh38.p7 | 11:45935770 | AAAAAAAAAAGGAAC[A/C/G]GTTTTTGACAATTAA | 51317 |
rs375519571 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46116014 | ACTTTCTAAAGGGGG[A/C/T]AATTTCAAAAGAATA | 51317 |
rs375633001 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45992328 | ATGAGGTCAGGAGAT[A/C]AAGACCATCCTGGCT | 51317 |
rs375654133 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46068554 | GATATGTTCTATGCA[A/G]AAGAAAAAAGACAGA | 51317 |
rs375659188 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46092159 | GGATCAGGCACACGA[C/T]GTCTACCTAGTCAAA | 51317 |
rs375664047 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45984190 | AAAAGAAAGCTGGAA[A/G]GAACAAAGACGGAAG | 51317 |
rs375722056 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46113551 | TTTAATTGTTTTGGC[C/T]GGGCGCGGTGGCTCA | 51317 |
rs375739459 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46011984 | CCAGATGACTATCAC[A/C]TTCTTTACTTCCTGT | 51317 |
rs375747597 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46036960 | AGGCAATCCTCTCAC[C/T]TCAGCTTCCCAAAGT | 51317 |
rs375764059 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46043415 | TTTCCTCAAATTAAT[A/C]CTTTCTGGTTAACAT | 51317 |
rs375764745 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45935915 | TTCTGTGTACAGTAT[A/G]CTAAAACTGTCAGTG | 51317 |
rs375770563 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45984621 | AGTCACGTTCCATGG[C/G]TTTTGTCAACAGAGA | 51317 |
rs375773738 | snp | C/T | 1.64993e-05 | 0.00287218 | intron-variant | PHF21A | GRCh38.p7 | 11:46076737 | TAAAAATATGCCCCC[C/T]TCCCCTTTTCCCCTA | 51317 |
rs375815592 | snp | C/T | 1.64741e-05 | 0.00286998 | intron-variant | PHF21A | GRCh38.p7 | 11:45979749 | CTGCAATGTTCCATC[C/T]ACACATTTACCTGTG | 51317 |
rs375823098 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46029274 | AATACTTGTTGAATT[C/T]TTCCTCACATAATAG | 51317 |
rs375838480 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46012894 | TTTACATCTAATTAG[G/T]CTTTGCACTGTCTTG | 51317 |
rs375840628 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46116414 | TTGAACCATGACATC[C/T]GTTACTCTGTCAATA | 51317 |
rs375853627 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46117034 | TTACTTTCTCAACTG[A/G]TATGGAAAAAGTTAG | 51317 |
rs375906197 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | PHF21A | GRCh38.p7 | 11:45965264 | AGCCCAGCAGCCATA[C/T]GCCTCAACGACAAGG | 51317 |
rs375955278 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46100286 | AAAAAAAAAAAATCC[C/G]ATGAGCATGGACTTT | 51317 |
rs375962099 | snp | C/T | 1.65444e-05 | 0.00287609 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45965449 | CAGTCTGCCCATTGA[C/T]GACACGGACGGGGTG | 51317 |
rs375964519 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46005690 | AACATTAGGGGAACC[A/G]TCAGCACCAACTACT | 51317 |
rs375969390 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46014164 | CCCTTGCTCCCATCC[G/T]TCCCTACTCACTTGT | 51317 |
rs375980932 | in-del | -/ATGT/ATGTATGTATGTATGT | | | intron-variant | PHF21A | GRCh38.p7 | 11:45987251 | CTGTATCATAAATAA[-/ATGT/ATGTATGTATGTATGT]ATGTATGTATGTATG | 51317 |
rs375993601 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45991279 | GTACCTTGATTTTTT[-/T]CCATATGGTCTAATG | 51317 |
rs375997507 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45990969 | AACATATAATGACAT[A/C]CAGCCACCATTATAC | 51317 |
rs376002458 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46096991 | AGTCATCTTAAGACT[C/T]TTCTTTTACCACACT | 51317 |
rs376018191 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46047073 | CAAGTAACAAACTTT[C/T]AGAAAATAAATGTAG | 51317 |
rs376023086 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45964067 | CCAGGCATGGTGGCT[A/G]ACGCCTGTAATCCCA | 51317 |
rs376036340 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PHF21A | GRCh38.p7 | 11:45949216 | TCTGCTGAAACTTAG[A/G]AAAAAAACCTAAGGG | 51317 |
rs376039512 | snp | A/T | 0.000296477 | 0.0121717 | intron-variant | PHF21A | GRCh38.p7 | 11:45949385 | TGAGGGAAGGGCCAG[A/T]TGCTGGCCAGTAATA | 51317 |
rs376077902 | snp | C/G | | | intron-variant, utr-variant-5-prime | PHF21A | GRCh38.p7 | 11:46117995 | AGCTGTAATAAGTAG[C/G]AAGACCCTCAAAATT | 51317 |
rs376080912 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46109636 | ACAAATGTACCAATG[C/T]GTATACTGTTAAGAA | 51317 |
rs376095916 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46062810 | ACAACCCAGACATAC[G/T]AAGGCATTTACTGAA | 51317 |
rs376122550 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45961642 | TGAATTGACGACATG[A/T]TACATAGAAGTCTTT | 51317 |
rs376126142 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46018150 | AGCTACTTGGGAGGC[G/T]GAGGCAGGAGAATGG | 51317 |
rs376136660 | in-del | -/A | 0.216048 | 0.247684 | intron-variant | PHF21A | GRCh38.p7 | 11:46025188 | ATATGTATACAGATT[-/A]AAAAAAAAAAAACAA | 51317 |
rs376141710 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45978117 | CCAGCCTGGCCAATA[C/T]GGTAAAACCCTGTCT | 51317 |
rs376146693 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PHF21A | GRCh38.p7 | 11:45939224 | AAGAGTTTTATTATG[C/T]TTTGGTAGAGGACAA | 51317 |
rs376160772 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45995400 | CCCCTAACAGGAAGG[A/G]ATCATTCTTACACAG | 51317 |
rs376239944 | in-del | A/GAG | | | intron-variant | PHF21A | GRCh38.p7 | 11:46021074 | TTTAAAAAAAAAAAA[A/GAG]AGAGAGACAAGGTCT | 51317 |
rs376246713 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46105651 | TGAATGAGTCTAAGC[A/T]ACTTAAAAATCATAA | 51317 |
rs376264118 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46080285 | CACCTCAGCCTCCCG[A/T]GTGGCTAGGACCCCA | 51317 |
rs376272526 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46113568 | GGCGCGGTGGCTCAC[A/G]CCTGTAATCCCAACA | 51317 |
rs376282694 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45951954 | TGGGACTATAGGCAC[A/G]CGCCACTGCATCCAG | 51317 |
rs376350658 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46073720 | TCAGAGCACATTCCT[C/G]TATCATTAAAATACT | 51317 |
rs376355930 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46016179 | CACTATAATCTTATG[A/G]GACCACCATCATATA | 51317 |
rs376359420 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45942469 | TTTGGCAATACTTCA[A/G]CTGAGAAAAAGTTGG | 51317 |
rs376365191 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45969755 | AGGCTACTTAGAAAG[A/G]GCCCATGAGGATTTC | 51317 |
rs376405992 | snp | A/G | | | intron-variant, utr-variant-5-prime | PHF21A | GRCh38.p7 | 11:46118126 | AAGACTGAATAGGAA[A/G]AAGGATGGACCCTTC | 51317 |
rs376463209 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46107524 | AAACTGCTACATTCT[-/T]ACCAGGTCCAATTCT | 51317 |
rs376485879 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46064115 | ACTCCACAGGAAAGG[A/C]GTTGTTAATTTTTTC | 51317 |
rs376542909 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46111610 | TGGCTAAGCAAGTAA[A/G]AAAGGCACTGCCCTG | 51317 |
rs376547964 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46065966 | GTTAGGGCGGGCACA[A/T]CCAAGAGATGACAAA | 51317 |
rs376559174 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46014616 | AACTAATTTACATTC[C/T]CACCAACAGTATATG | 51317 |
rs376567404 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46065188 | GGAGAAAATCTCCAG[C/G]TCCAGGACACAAATC | 51317 |
rs376577759 | in-del | -/CAC | | | intron-variant | PHF21A | GRCh38.p7 | 11:45948593 | ACATGGGGTTCTGTT[-/CAC]TGTGCTATTCATGGA | 51317 |
rs376591323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45952125 | TTTTGATGATAGAAT[A/G]AAAAGCTGTCAAAAA | 51317 |
rs376651509 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45955048 | ACTGTGGCAACCAGT[-/T]GCTCTGGGGCACAAA | 51317 |
rs376661614 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45957852 | CAAAAGGTGAATCTT[C/T]GAAAAGAATAACAAA | 51317 |
rs376664005 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46021660 | GATCCTCCTGCCTCA[A/G]CCTCTCAAGTCTCTG | 51317 |
rs376685241 | snp | A/C | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45932578 | TCTCCAGTTCTGACA[A/C]CTTTTTAATAGAAAT | 51317 |
rs376709714 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46060801 | ATAGTTTCATTTGCT[A/G]TGCAGAAGCTCTTTA | 51317 |
rs376717186 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46086801 | AATTCACATAAACTC[C/T]GGAAATGAACGGCAG | 51317 |
rs376734638 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46009963 | ATTTTCATTAAATAA[A/G]TATCCTAATTTGTTC | 51317 |
rs376739810 | snp | C/T | 1.71278e-05 | 0.00292637 | intron-variant | PHF21A | GRCh38.p7 | 11:45938127 | CTTTGTCCTCCTCGG[C/T]CCCTCCCCTGTTGGA | 51317 |
rs376740465 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45984474 | CAAGACAGGTAGTCA[C/T]GGTGATCAATATTGT | 51317 |
rs376744076 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45931755 | CAGGGCCAGGGTACA[G/T]AGCCTCCACCGCCCT | 51317 |
rs376748069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45985979 | TTAAAATTCTCTGCA[C/T]GGATGTTTAACAGAT | 51317 |
rs376758846 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46094664 | AAAGTGGGTGGATCA[C/T]GAGATCAGGAGATCG | 51317 |
rs376760054 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46109796 | AGACCAGTCTACCCA[A/G]CATGGTGAAACCGTC | 51317 |
rs376784157 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45994873 | GCTTTGAATGTCTCC[C/G]TGGTATTTCTCTGTC | 51317 |
rs376784976 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46041660 | ATGAAGACCCAGATT[C/T]AAAACAAAGAAAACA | 51317 |
rs376794452 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46012681 | GTAAGTAAATCTATA[C/T]CTCTAGTGCTGGCCT | 51317 |
rs376825223 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:45961801 | GGAGAGGACAAGGAC[-/A]GGGGAGGTGATGTGA | 51317 |
rs376845222 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45991832 | TTACCTCTATAGCAC[C/T]GCACAGAGAAAAATG | 51317 |
rs376852559 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46067883 | AGGCACAAGTACCAA[A/G]TACCATGAGTACACA | 51317 |
rs376862003 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46031336 | TTCTTCCTTTCCATA[C/T]AGCACTGCCAGATTA | 51317 |
rs376869895 | snp | C/T | 0.00557542 | 0.0525036 | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45929394 | AGCTGCTCTGTATCC[C/T]CCCCCACCCCCTCAA | 51317 |
rs376876604 | snp | A/G | 1.65594e-05 | 0.0028774 | intron-variant | PHF21A | GRCh38.p7 | 11:46076710 | AGCAGACATATCTTT[A/G]GAACACAACGTTAAA | 51317 |
rs376878944 | in-del | -/TG | | | intron-variant | PHF21A | GRCh38.p7 | 11:46008287 | CAATTGAAATTTTCC[-/TG]TGTGTGTGTCCTTAT | 51317 |
rs376888297 | in-del | -/AGGAA | | | intron-variant | PHF21A | GRCh38.p7 | 11:46079851 | GAAAGGAAAGGAAAG[-/AGGAA]AGGAAAGGAAAGGAA | 51317 |
rs376930194 | in-del | -/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45981940 | TCTCTTTTTGTTTTT[-/C]TTTTTTTTTTTTTTT | 51317 |
rs376976172 | snp | C/T | 0.000153988 | 0.00877328 | missense, utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:46076812 | AGCTGTTTCTTTAAG[C/T]CAGCATTCTGATTGG | 51317 |
rs376981110 | snp | C/T | 1.64893e-05 | 0.0028713 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934132 | TGGAGAGGTCGATGC[C/T]GTGGATGAGGCGAAT | 51317 |
rs377000937 | snp | C/T | 5.03799e-05 | 0.00501871 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45969834 | GGAAGAAAGTTTGGA[C/T]GTGGAGTGAGTCTAG | 51317 |
rs377010277 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45941649 | ATACAGAACCGGCTC[C/T]TTGCCTAAAAAGAGC | 51317 |
rs377034785 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46018118 | AGCCGGGCGTAGTGG[C/T]GGGCGCCTGTAGTCC | 51317 |
rs377098329 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46042454 | ACAGGCCAGGGACAC[A/G]TTATAAGACTGGACT | 51317 |
rs377100266 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46076216 | GATGTTCTTCTCCTG[C/T]CCTATATAGAATAAG | 51317 |
rs377120635 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PHF21A | GRCh38.p7 | 11:46112707 | TCTGAAATTAAATAC[C/T]GGCACAGAAAACCTT | 51317 |
rs377133610 | snp | C/G | 1.71023e-05 | 0.00292419 | intron-variant | PHF21A | GRCh38.p7 | 11:45934250 | ATGACAAGGGCAGTG[C/G]CACTGAGCCGCCTGG | 51317 |
rs377190327 | snp | C/T | 0.000141161 | 0.00840002 | downstream-variant-500B, stop-gained, synonymous-codon, utr-variant-3-prime | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45928837 | CCCCAGAGCCCTGCC[C/T]GAGGCTGAGGCTGGG | 51317 |
rs377198834 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45967332 | GAGATAGTGCCACTG[C/T]ACTCCAGCCTGGGTG | 51317 |
rs377208245 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45976367 | AATTCTTGAAAATAG[A/G]AACTCTCTGATTTGT | 51317 |
rs377225039 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | PHF21A | GRCh38.p7 | 11:46038374 | CTCAAGTGATCCACC[C/T]GCCTCAGCCTCCCAA | 51317 |
rs377235822 | snp | A/C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46037555 | CTGAGGCAGGACAAT[A/C/T]GCTTGAATCCGGGAG | 51317 |
rs377250717 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46098898 | TGAGAACCCTTTCTA[C/T]TGCACTAACTGTAAC | 51317 |
rs377331573 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45987029 | CATCCCAGATTTCTT[A/G]TACCTCTATGGTGGT | 51317 |
rs377335686 | snp | A/G | 0.000556638 | 0.0166736 | intron-variant, stop-gained, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45935237 | CGGATGGGCCCACTC[A/G]CTCAGGTGACTAGGA | 51317 |
rs377348550 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45971554 | CTACAGAGAAAGGCA[A/G]TCTCTAGTTTTCAAG | 51317 |
rs377350218 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | PHF21A | GRCh38.p7 | 11:46115256 | ATGGCTGAACCTCAC[A/C]TATAATTTCTAAAAG | 51317 |
rs377350910 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45955957 | AACTAGTTTGACTGT[A/T]AACTTGTGAAGGACT | 51317 |
rs377353890 | snp | C/T | 1.64868e-05 | 0.00287109 | synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45950240 | TACCAACCCTAGAGA[C/T]ACCATGAAGGCAAGT | 51317 |
rs377364377 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45987286 | TATGTATGTATGTAA[C/G]CTGACCCATCAAAGA | 51317 |
rs377373121 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46018025 | GGAGGCCGAGGCGGG[A/C/T]GGATCACGAGGTCAG | 51317 |
rs377406433 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45963360 | GGGAGGTGGAGGTTG[A/C]AGTGAGCTGAGATCC | 51317 |
rs377421334 | snp | C/T | | | upstream-variant-2KB | PHF21A, LOC105376661 | GRCh38.p7 | 11:46123043 | TTTTGTTTTTAAAGC[C/T]CAGCACTTTTGTAGC | 51317 |
rs377425089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46056462 | GTTCTCAAATTAGTA[C/T]GAGCTAATATCACAG | 51317 |
rs377436640 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46030818 | CATAGTGTGTGTGTG[C/T]GCGTGTGTGTGCGTG | 51317 |
rs377491821 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46022429 | CACTGCACTCCAGCC[C/T]GGGCAACAAAGTGAG | 51317 |
rs377494614 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45975809 | ATTGCTTTCTCTACG[C/T]CTTGGTATATGCCAA | 51317 |
rs377546343 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46115405 | ATATAAGAATTATAC[A/G]AAAGCCTACAAAATA | 51317 |
rs377599410 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46113445 | GAAAAAGCAAAAAAA[-/A]CTTGATGAATAAAAA | 51317 |
rs377627425 | snp | C/T | 2.39037e-05 | 0.00345706 | intron-variant | PHF21A | GRCh38.p7 | 11:45965634 | AAGAGAGAATAATTA[C/T]TGTATTACTTAAGCT | 51317 |
rs377627620 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46099965 | AGTCCAACATATTGA[G/T]CCTTTCTCACCACTG | 51317 |
rs377635061 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46108912 | ACGCACTATGCTTGG[C/T]AATGGATATACAAGG | 51317 |
rs377652694 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46000521 | AAAGACTCTATAACG[C/T]TTTTCTTTTGAAAAG | 51317 |
rs377655058 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45969332 | GAAAGTCCTCTGTAC[A/G]GACCCCTAGCCTAAG | 51317 |
rs377658544 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46080550 | CTATAAACAATAGGT[G/T]CCTTACAAAAAAGGT | 51317 |
rs377664648 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46005245 | CACCTGACCTCAAGT[G/T]ATAGATCATAGTCAA | 51317 |
rs377667851 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45980479 | AAAGTACTCAGAACT[A/G]TGATTGGCACATTGT | 51317 |
rs377669384 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45945398 | GCTCAACAGTTTCTG[A/C]TCAACAGTTGCTCTA | 51317 |
rs377700825 | snp | A/C/T | 8.44959e-05 | 0.00649929 | synonymous-codon, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934031 | GGAGGGGGAAGGGGC[A/C/T]GGCGTGGAGGTGGCG | 51317 |
rs377702246 | snp | A/G | 0.000347687 | 0.0131804 | intron-variant | PHF21A | GRCh38.p7 | 11:45953491 | AATAAACCATACACC[A/G]TAGACTGAGACCTGC | 51317 |
rs377734291 | in-del | -/T/TTTCTTTTTTTTTTT | | | intron-variant | PHF21A | GRCh38.p7 | 11:45971890 | GTGTCTTTTTCTTTC[-/T/TTTCTTTTTTTTTTT]TTTTTTTTTTTTTTT | 51317 |
rs377755781 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46096186 | TCTCTTACCCTCTCC[G/T]GGACATTCCTCTAGC | 51317 |
rs377762575 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46082291 | GAAATGCAACAAAGC[A/G]TGGCTTTTGTCCCAC | 51317 |
rs377765542 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PHF21A | GRCh38.p7 | 11:46105027 | TTAGTACTTACTATG[C/T]GTCAGGCACTTCTAC | 51317 |
rs386373756 | in-del | -/AA | | | intron-variant | PHF21A | GRCh38.p7 | 11:45989491 | ACCCCATCTCTACTA[-/AA]AAAAAAAAAAAAAAA | 51317 |
rs386373757 | in-del | -/AA | | | intron-variant | PHF21A | GRCh38.p7 | 11:45989509 | AAAAAAAAAAAAAAA[-/AA]ATACAAAAAATTAGC | 51317 |
rs386373758 | in-del | -/TT | | | intron-variant | PHF21A | GRCh38.p7 | 11:46092760 | AGATGTGTCTCACCT[-/TT]TTTTTTTTTTTTTTT | 51317 |
rs386373759 | in-del | -/TT | | | intron-variant | PHF21A | GRCh38.p7 | 11:46092774 | TTTTTTTTTTTTTTT[-/TT]TGAAACAATGTCTTA | 51317 |
rs386753193 | multinucleotide-polymorphism | AC/GA | | | intron-variant | PHF21A | GRCh38.p7 | 11:45976634 | ATCACTTGAGCTCCG[AC/GA]GTTTGAGACCAGCCT | 51317 |
rs386753194 | multinucleotide-polymorphism | AAG/GAA | | | intron-variant | PHF21A | GRCh38.p7 | 11:45998612 | CCACCTCCCAGGTTC[AAG/GAA]TGATTCTCCTGCCTC | 51317 |
rs386753195 | in-del | AGACTCTATAAC/GCTTTAAAGACTCTATAAT | | | intron-variant | PHF21A | GRCh38.p7 | 11:46000508 | TTTAAACAGCTTTAA[lengthTooLong]GTTTTTCTTTTGAAA | 51317 |
rs386753196 | in-del | ACCAACCTTCTA/CTCT | | | intron-variant | PHF21A | GRCh38.p7 | 11:46035420 | TCTAGTATGTTTTGA[ACCAACCTTCTA/CTCT]GTTGGTTACTTCATT | 51317 |
rs386753197 | multinucleotide-polymorphism | AT/TA | | | intron-variant | PHF21A | GRCh38.p7 | 11:46039197 | CAAATCTTACTGAGA[AT/TA]ACTAATGAAACGTTT | 51317 |
rs386753198 | multinucleotide-polymorphism | AC/CT | | | intron-variant | PHF21A | GRCh38.p7 | 11:46089961 | CCTGGACCCCTCCCT[AC/CT]CATCATCAGTGCTCA | 51317 |
rs386753199 | multinucleotide-polymorphism | AAA/GAG | | | intron-variant | PHF21A | GRCh38.p7 | 11:46115178 | TGAAAGGGAGAAGTG[AAA/GAG]GAGTATTCAAATTGC | 51317 |
rs397705535 | in-del | -/T | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45974628 | TGGCTAATTTTTTTT[-/T]ATTTTTAGTAGAGAC | 51317 |
rs397708802 | in-del | -/C | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46110571 | TTTTCTATATTGGCC[-/C]ATTAACACCAGGGAC | 51317 |
rs397710298 | in-del | -/TTA | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45978356 | AATCCTAAGAGGAAG[-/TTA]TTATTATTACCATCT | 51317 |
rs397718456 | in-del | -/CT | | | intron-variant | PHF21A | GRCh38.p7 | 11:45962310 | ACGGGTTTGGTAACT[-/CT]GTGAACAGGTGTGAA | 51317 |
rs397722590 | in-del | -/A | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45970594 | CAAGTTTTGTTCAGG[-/A]AAAAAAAAAAAATCC | 51317 |
rs397727935 | in-del | -/G | | | upstream-variant-2KB | PHF21A, LOC105376661 | GRCh38.p7 | 11:46123027 | TGGGGGGGTGGGGGG[-/G]TTTTGTTTTTAAAGC | 51317 |
rs397733115 | in-del | -/T | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46095197 | AAATAGAATATTTGC[-/T]TTTTTTTTTGACAAT | 51317 |
rs397737192 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45951824 | TTTTTTTTTTTTTTT[-/T]GAGGCGGAGTCTCAC | 51317 |
rs397740160 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45998530 | TTCTTTTTTTTTTTT[-/T]AAACAGAGTTTTGCT | 51317 |
rs397742571 | in-del | -/AC | | | intron-variant | PHF21A | GRCh38.p7 | 11:46114104 | CACACACACACACAC[-/AC]GCACACATCCCCACA | 51317 |
rs397766658 | in-del | -/A | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46067612 | CAAAAAAAAAAAAAA[-/A]CTGAATTGAATCATT | 51317 |
rs397783389 | in-del | -/AG/AT | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45931275 | GAAAAGGTAAGTTAG[-/AG/AT]GTGTTGTGTGGCAAC | 51317 |
rs397793375 | in-del | -/G | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46089053 | TTTTAGGGACAGTTT[-/G]GGGGCACACTGTGTC | 51317 |
rs397799545 | in-del | -/TT | | | intron-variant | PHF21A | GRCh38.p7 | 11:45966196 | TATGTACTGAAGACT[-/TT]CACACTTTTACCTCA | 51317 |
rs397803889 | in-del | -/T | 0 | 0 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46119758 | TGCTGTTAGGATTTC[-/T]TTTTTTTTTTTTTTC | 51317 |
rs397806172 | in-del | -/TT | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46092775 | TTTTTTTTTTTTTTT[-/TT]GAAACAATGTCTTAC | 51317 |
rs397812175 | in-del | -/TT | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45943140 | ttttttttttttttt[-/TT]gagacagggtcttgt | 51317 |
rs397847961 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46003285 | AAAGGCTAACATTCA[-/A]AAAAAAAAAAAAATG | 51317 |
rs397848568 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46003284 | TAAAGGCTAACATTC[-/A]AAAAAAAAAAAAAAT | 51317 |
rs397943601 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:45950540 | TTCAAAAAAAAAAAA[-/A]TCGCAAAAAAAACTC | 51317 |
rs397949998 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46096390 | GTAACCATACTCCCT[-/T]CTAATTCCTCTCCTC | 51317 |
rs398015935 | in-del | -/T | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45957226 | TAATCTCTGCACAAG[-/T]TTTATCCATTACTTA | 51317 |
rs398015936 | in-del | -/T | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45967384 | TTTAGCAATAAGGGA[-/T]TTTTTTTTTTTTTTT | 51317 |
rs398015937 | in-del | -/T | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45987687 | CAATGATTCAGGTGC[-/T]TTTTTTTTTTTTTTT | 51317 |
rs398015938 | in-del | -/T | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46071744 | ATAGGGTGTTTCCAG[-/T]TTTTTTTTTTGGCTA | 51317 |
rs398015939 | in-del | -/A | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46079430 | TTAAATTCCTTTCGG[-/A]AGCCACTGTCACCCG | 51317 |
rs398015940 | in-del | -/A | 0 | 0 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46084697 | GCGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 51317 |
rs398015941 | in-del | -/T | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46118435 | GAATATTCCAGGGGC[-/T]TTTTTTTTTTTTTTT | 51317 |
rs398015942 | in-del | -/G | 0 | 0 | upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46122114 | TCGGGCCGCGGAGTT[-/G]GGGGGGGCCGCCGCG | 51317 |
rs398045175 | in-del | -/T | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46028104 | CAATTTTTTTTTTTT[-/T]GAAGGATGGGCTTGA | 51317 |
rs398075911 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46016983 | TGGATTTTTTTTTTT[-/T]TAATTGAGATGGAGT | 51317 |
rs398075912 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46071743 | ATAGCCAAAAAAAAA[-/A]ACTGGAAACACCCTA | 51317 |
rs398075913 | in-del | -/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46110570 | ATTTTCTATATTGGC[-/C]CATTAACACCAGGGA | 51317 |
rs398115351 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46109561 | AACACAAAAGCTCAT[-/T]AATTAAAATTTTTCA | 51317 |
rs527252447 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46063425 | ATACTGTCTTTGTCA[C/T]GACTACTTAACTCTG | 51317 |
rs527268473 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46005204 | CTTTTTGAGCACTGA[C/T]GTGATGCCACAACTG | 51317 |
rs527283221 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46038461 | ACTATTTATTGAGCA[C/T]CTCCATGTGCTACAT | 51317 |
rs527284087 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46085831 | TTCTTGTGAATATGA[A/G]TTTTCAATATATTTG | 51317 |
rs527321594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45976510 | ACCACTGCTCTTTGT[A/G]TACCAGAATCTACCA | 51317 |
rs527376324 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46077132 | TTTATAGAAAGTATC[A/C]ATTGACAGAAAACCC | 51317 |
rs527389712 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45959781 | GGAACAGGAGAAAAT[A/T]TTTGCAAATCATGTA | 51317 |
rs527391479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45968500 | CTGGAACTACATACA[C/T]GTTCTGTCCTCTGCC | 51317 |
rs527392286 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46009919 | TGTTTCCTTGAAACA[C/G]ATAAAGGGGCCGTCA | 51317 |
rs527421761 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46035462 | GTACATATTCAGTAC[A/G]CTACATTGTGTTAGC | 51317 |
rs527439912 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45984392 | GACATTCGCATCACT[G/T]GGTTTCATCAGGGCT | 51317 |
rs527444990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46026935 | TGGAGAGACTGTTGA[A/G]TGTTTGGAACACAGA | 51317 |
rs527478871 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45933600 | TGCTCTCCTCCCTCC[A/G]CCCGTCCCTGCTCCC | 51317 |
rs527485692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46050763 | TTAAAATTGAGGAAA[C/T]AGGAACACATCAGCC | 51317 |
rs527494555 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46101477 | GTTAGGGAATAGGTA[C/T]GTGGGGTTATATTAT | 51317 |
rs527556563 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46034803 | ACCCAGTTTCCCAGG[A/T]TATAGTGATTGGTCT | 51317 |
rs527574048 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45975879 | CTCCCCCTGGCCCCC[C/T]GATTGCTACTTAATA | 51317 |
rs527591742 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46033691 | GCCATATATGGCTAT[G/T]GAGCACTTAAAATAT | 51317 |
rs527593778 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46042801 | CACCTTCTTGCTATG[A/T]CCTCACAGCAAGAAG | 51317 |
rs527611410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45972026 | AAACATGTTAGCCAA[C/T]GAGTATATAGTAAAT | 51317 |
rs527616005 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46010498 | CTGACTCTAATGCCT[A/G]AATTTCTTTCTGCTT | 51317 |
rs527635969 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930227 | GAGGTGGCTGGAGAG[A/G]CAGCCGTGCATGCGG | 51317 |
rs527664790 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45948833 | AAGGAGAAGAAACAC[A/G]CACACAAAGCAAAAG | 51317 |
rs527705661 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46017282 | GGCCTACATCTATTA[A/T]TTTTTAACAGGCATA | 51317 |
rs527711617 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46117601 | TTTTTCAACACACTA[C/T]ACCCCTTTCCAAAAT | 51317 |
rs527722659 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46066780 | ACGTGCTAGCTCTCT[A/T]GAACCTCACTTCTTA | 51317 |
rs527729242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45957622 | TACCAAAACTTATGC[A/G]ATGCTGTGAAAGCAG | 51317 |
rs527772809 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46056970 | CTTAAAGATAACTGA[C/T]TTTATTTGCTTTAAA | 51317 |
rs527773782 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45963077 | CAAATTACAAAATAC[A/C/G]TAAGTTTGATTTTGG | 51317 |
rs527785709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46110330 | TAAGACCAAGTCTTC[C/T]GACATCATCACAACT | 51317 |
rs527798574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46118574 | TTTATAAACATTAGC[A/G]TAACTGTACACAAAA | 51317 |
rs527802657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46058512 | CCTGATAATTATTTG[C/T]CAAATGAATTGAGGT | 51317 |
rs527803898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45940058 | TCCACCACCACTAGT[A/G]AAGGAACACATCGTC | 51317 |
rs527803903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45949268 | TGATAAGTCAAAAAA[A/G]ATCTACCACTTCACA | 51317 |
rs527814291 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46001256 | AAACTGAAAAACCAT[A/C]AAGGTTAAGTCAAAG | 51317 |
rs527835704 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46079953 | ACTTCTAAAGACATC[A/G]CTGCCCAAAGTTAAC | 51317 |
rs527853193 | snp | A/G | 6.71419e-05 | 0.00579365 | intron-variant | PHF21A | GRCh38.p7 | 11:45965621 | AACCTATAGGGGAAA[A/G]AGAGAATAATTATTG | 51317 |
rs527909995 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46107238 | CCATAATTTTTAAAA[A/G]TGTAGAGAGTACTGG | 51317 |
rs527920714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45983331 | GAAAAAGAAAGAGAG[C/T]TCTGCATTACAGGTC | 51317 |
rs527958707 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46074663 | ATGTGCCACTACACC[C/T]GGTTAATTTTTGTAT | 51317 |
rs527990156 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46025606 | CTTATAATCTCATTT[A/T]AAAAATTTTCACTTT | 51317 |
rs527994391 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45966539 | GCTTGGGTTCAAATC[C/T]TAGTTCTACCACTCA | 51317 |
rs528000468 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45968148 | AAGATTCTCTCAACA[C/T]TGGTTATTACCATTA | 51317 |
rs528003172 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45933588 | GGATCTGAAACCTGC[C/T]CTCCTCCCTCCGCCC | 51317 |
rs528032292 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PHF21A | GRCh38.p7 | 11:46062960 | TGACAGAAGGATGAG[C/T]GAGACGACCAAGAAC | 51317 |
rs528035916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46024079 | AGTTGCAATTGGTTA[C/T]GAAAGCAAGGAAAGG | 51317 |
rs528039828 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46002951 | TAAATGAATTCAAAT[A/C]AAATGAATTAATTGG | 51317 |
rs528079895 | snp | A/G | | | upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46122227 | AAGGGGGGGGGGGAA[A/G]GCCGTGAGGGGCAGG | 51317 |
rs528084200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46054035 | TTTTTCACAAGCAAC[A/G]TCGTGGCAGTGGAGG | 51317 |
rs528108221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46062330 | GTCTCAGAACTTTTA[C/T]TAGCCAGGCATGAGA | 51317 |
rs528111209 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | PHF21A | GRCh38.p7 | 11:46114103 | CACACACACACACAC[A/G]CGCACACATCCCCAC | 51317 |
rs528116126 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46006311 | CAAAAAACCATGAGA[A/T]ATCAGTAAATTCTTA | 51317 |
rs528116601 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46072044 | TATACTAGGAATAAA[A/C]AAGCAAATAAAACAA | 51317 |
rs528136640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45937140 | GCTGCAGGATGAGGA[C/T]AATATTACAAGGGAA | 51317 |
rs528154938 | in-del | -/T | | | intron-variant, utr-variant-5-prime | PHF21A | GRCh38.p7 | 11:46118056 | TCCTGCTGGATAGCA[-/T]TTAGAGATCTTCATG | 51317 |
rs528164393 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45951001 | ATTTCTCTCTGAAGA[C/T]CACTCTTAGGGCTCC | 51317 |
rs528171932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46105951 | CAATGTATTTAATTA[C/T]ACAAATATAAGTATT | 51317 |
rs528192552 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:46054884 | CTTTTAACCAGTAAC[A/G]ACTAGGACCAGCAGT | 51317 |
rs528195571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45945700 | AGCTGCCTTACATGG[C/T]ATAAAAAGCATTCTA | 51317 |
rs528200336 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:45982103 | CTGGGACTACAAGAG[C/T]GTGCTACCATGCCCA | 51317 |
rs528208590 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46114684 | AAAATTTAAAAAAAA[A/C]ACACACAATTTAGGG | 51317 |
rs528228626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46006868 | AAATACAAATCAACA[A/G]GTACTAACAATATGT | 51317 |
rs528230906 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45997830 | CATTCTGCAATTTCA[A/T]CCTCCCTCACCAGCA | 51317 |
rs528248030 | in-del | -/AAGG | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46072096 | AACTAACAATCTAAT[-/AAGG]AAGACAGATATTTAA | 51317 |
rs528254988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45961682 | TGGCAGTGGGGTGGA[A/G]AAGAAACATAATTCC | 51317 |
rs528271782 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46020385 | CAAGAACCAGGAGCG[A/C]CTGCTCTGACACTGT | 51317 |
rs528306728 | in-del | -/TAAA | | | intron-variant | PHF21A | GRCh38.p7 | 11:46004760 | CTGTCTCCTCAAGAC[-/TAAA]TAAAGGACTCATCAT | 51317 |
rs528325513 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45978827 | TTAAATTGTATGCTT[A/G]TTTAAATGCCCTTTT | 51317 |
rs528334982 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46078779 | TTTGGGGTCTCTTTT[A/C]ATAATATTGGGATGA | 51317 |
rs528338017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46013436 | ATAATGGCCCCAAAG[C/T]GAAAGAGTAGTGATG | 51317 |
rs528380918 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45962290 | GTCATAGAGAGAACG[C/T]TGGATACGGGTTTGG | 51317 |
rs528384239 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45998894 | GTGGTGTGATCTCAG[C/G]TCACTGCGGCCTCTG | 51317 |
rs528466985 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46095971 | TACTATACCAAGCTG[A/C]TAGAGGCCCCCAAAC | 51317 |
rs528483705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45995924 | ATTATTTTCAGTATA[C/T]GGCTTTTTTTAAAAA | 51317 |
rs528493774 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45935509 | AACTGCATTTGCCCA[A/C]GTTAATCACGTTAAT | 51317 |
rs528494951 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45986667 | TTCCTTCAGAAAAAT[A/G]TTGGGAATCAAATTA | 51317 |
rs528499254 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46079977 | AGTTAACAATAACCA[C/T]AGACAGAAGAATATG | 51317 |
rs528570417 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:46087766 | TATTTTGAAAAAATT[C/T]TTTTCCTGAGATAGG | 51317 |
rs528589889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45978173 | GGCATGGTGGCACGC[A/G]CCTGTAGTCCCAGCT | 51317 |
rs528613492 | snp | A/G/T | 0.000572099 | 0.0169035 | downstream-variant-500B, utr-variant-3-prime, synonymous-codon | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45928855 | GGCTGAGGCTGGGCC[A/G/T]GCGCTGCCCCTCATC | 51317 |
rs528626238 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46017198 | CTGGTCTCAAACTCC[A/C]GACCTCAGGTGATCC | 51317 |
rs528661646 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:45951241 | ACATCTTCAATTGTA[A/G]AAGACATACTCCTGT | 51317 |
rs528680626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46011457 | AGATGGTGCCACTGC[A/G]CTCCAGCCTGAGCGA | 51317 |
rs528711676 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46120564 | GGGTGGAGGGCAGAG[A/G]GGAGGGGGGGGAGCC | 51317 |
rs528726926 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45960745 | GAATTCATGGATATC[C/G]CTTCGATGAATCTAA | 51317 |
rs528757165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45943933 | ATCAGACAATCCAAA[C/T]GGAGAGGCATTCTAC | 51317 |
rs528791025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46003992 | AAATGCTTCAATATA[C/T]TAAGTTTCAGCTGTA | 51317 |
rs528796372 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46122217 | CAGCAGTTTGAAGGG[C/G]GGGGGGGAAAGCCGT | 51317 |
rs528817810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46112011 | TGGATATTCTAACAG[C/T]GCAAACATTGTAAAC | 51317 |
rs528818371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45943171 | TCTGTCACCCAGGCC[A/G]GAGTGCAGTGGCGCA | 51317 |
rs528842875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46111632 | ACTGCCCTGCTTCTG[C/T]ATACATTCAAACTAA | 51317 |
rs528845918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45952203 | TGTTTATGGCAGTGA[C/T]TCTGTCCAACTAGAA | 51317 |
rs528854865 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46122387 | ACCCCGCCCCCTTTC[C/T]AAATAACTACCCTTG | 51317 |
rs528869395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45962129 | CTAGAAACTGAGTTC[C/T]GTGAGGGTACGGGCT | 51317 |
rs528907518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46113699 | GGCGTGGTGGCGCAC[A/G]CCTGTAGTCCCAGCT | 51317 |
rs528910654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46021066 | ATAGATTCTTTAAAA[A/G]AAAAAAAAAGAGAGA | 51317 |
rs528914359 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46012386 | TTCAAGTTTCTGTCC[A/G]GGCCTTCTTTGTTTC | 51317 |
rs528926740 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45967778 | GACTGAACTTAAAAC[A/G]ACCCTGTGGTGGGTG | 51317 |
rs528931546 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45961490 | AAAACAGAAATTTGA[A/C]GATAATGCATTGGAT | 51317 |
rs528971357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46006117 | GTTATTTTACATTTA[C/T]GATTAAAGAACCAGA | 51317 |
rs528974607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45944146 | GCAATCTGAATATGG[A/G]CTGTATATTTTATAT | 51317 |
rs528978600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45953098 | TGGTTGTAACAAAAA[C/T]GCACACTTAACAACT | 51317 |
rs528991243 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PHF21A, LOC105376661 | GRCh38.p7 | 11:46123340 | AAATTAAGTTTAGTT[C/T]CTCAAGAAAAAGCAA | 51317 |
rs528991673 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:45979162 | GCTGGGATTACAGGC[A/G]CCTGCTACCAGGCCT | 51317 |
rs528994763 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46062245 | TGGAATTATATGCCC[C/T]TCGGTTGTGGGACAT | 51317 |
rs529013494 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46005193 | AAAATCCAAAACTTT[G/T]TGAGCACTGACGTGA | 51317 |
rs529017042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46077628 | GGAACACATCTTCCT[C/T]GTCTATTAAATTTGG | 51317 |
rs529047492 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46087715 | TAGAGAAGGGGTCTC[A/T]TATGTTGCCCAGGCT | 51317 |
rs529054999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46036748 | TGATTTTACCTTGTA[C/T]ATGGACATCTTACTA | 51317 |
rs529057855 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45968907 | CTGCACTCCAGCCTG[G/T]GCGATGGGAGCGAAA | 51317 |
rs529083622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46095816 | TTAATTCACCCTACT[A/G]CAAATTTCAAATGAT | 51317 |
rs529091070 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46086844 | AGAACTTAACATTAT[A/T]CATAACAAAGGGCTA | 51317 |
rs529101469 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PHF21A | GRCh38.p7 | 11:45933146 | CCTGGACACACACAT[C/T]CTTCTTCCCTGCCTT | 51317 |
rs529142277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45987457 | ACAAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCA | 51317 |
rs529146148 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46117510 | TGTATTTATAAAGCC[A/G]AGTGCCTAAAAATTG | 51317 |
rs529154526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46019937 | TAATCATCATGTCAT[C/T]TCATTTCAAATTGTG | 51317 |
rs529184871 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45969942 | AAACCAGAGAGAACA[A/G]TTACTCTTCAATATC | 51317 |
rs529212921 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | PHF21A | GRCh38.p7 | 11:46028092 | AATCTCTGGGGACAA[C/T]TTTTTTTTTTTTGAA | 51317 |
rs529224940 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46115277 | TTTCTAAAAGCTTTG[C/G]AAGAGTTCACCATAA | 51317 |
rs529238607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45994857 | TGTCTAGTCATCACA[C/T]GCTTTGAATGTCTCC | 51317 |
rs529275349 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46088782 | AACTTCTCTACATAG[C/T]ATATATCTAGAAGAC | 51317 |
rs529275654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46050979 | TAAAGATAAATATAG[C/T]AGTCTCCGAGTTCTC | 51317 |
rs529296895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46060028 | GATTACAGGCGTGAG[C/T]CACTGCACCCAGCCC | 51317 |
rs529311397 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46044163 | AGATAAATAATAGCA[A/T]CTATTAACACAAGAC | 51317 |
rs529321202 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46111879 | AATCCTGTAACACTG[A/T]GAACTACAGTGATAG | 51317 |
rs529352106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46035961 | TTGCATTTTTGAAGA[C/T]TCACTCTAGCTACAG | 51317 |
rs529377545 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46032197 | AATCTCACAAAAAGC[A/G]AAAATATCATTATAT | 51317 |
rs529380846 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46094869 | CGCGCCACTACACTC[A/C]AGCCTGGCGACAGAG | 51317 |
rs529433199 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46048219 | GTCTCCAGGGAGGTG[A/C]ATATTCTAAACATTT | 51317 |
rs529434003 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46103103 | AATGGGACTGCACCC[C/T]CGTCACATACAGCAC | 51317 |
rs529456148 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46011863 | TATGCAACACAACAA[A/C]ACAAAAAGAGCAAAA | 51317 |
rs529482200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46010376 | ATACCTCGCAACAAT[C/T]TTGTGAAGATACTTT | 51317 |
rs529493550 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45949337 | GGTTTTCAGAGGGGA[C/G]GCACTGAACAGCTCA | 51317 |
rs529495781 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45959766 | AAAAAGGCAAACTAC[A/G]GAACAGGAGAAAATA | 51317 |
rs529504555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46067618 | AAAAAAAAAACTGAA[C/T]TGAATCATTTAAATG | 51317 |
rs529558339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46120351 | CCTCCCCGGCCGAGG[A/G]ACAGCCGAGGGGGGG | 51317 |
rs529564751 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46111289 | AGCCTGGCCAACATG[A/G]TGAAACCCCATCTCT | 51317 |
rs529570971 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45951115 | TTCTATTCTTTTCTT[C/T]GCTTGCATGTGGTCT | 51317 |
rs529600830 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46119692 | CTCGATACCAACCCC[A/T]CCCCTACCAGGGCCA | 51317 |
rs529628809 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46061579 | AATTAATTCTTTCCC[A/G]TACTTTCCAAAGAAA | 51317 |
rs529635466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45949938 | CTTCGCTGTGCTGTT[C/T]AGAAAAAGAAGAGCT | 51317 |
rs529638759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46048385 | ATTCTACTGTATGGA[C/T]ATACCACACTTTATT | 51317 |
rs529654304 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930947 | AGGGGACAGTGAAGG[A/C]CAGGGAGATTGGGTG | 51317 |
rs529659669 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45991084 | TCCTCTTTTTACTGC[C/T]TCCATAGTTCTACCC | 51317 |
rs529663768 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46110108 | ATAAATATCTTAAAA[C/T]CCAGCCCCTTATTGC | 51317 |
rs529675599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46047480 | TCTGGATAAAGAAAC[C/T]GAGACAAAAAGGTAA | 51317 |
rs529679882 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46099891 | AAAAAGAACCCTGAC[C/T]TTAGGCCTAAAAACT | 51317 |
rs529686309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45939047 | ACGTGTTAGCCAGGA[C/T]GGTCTCGATCTCCTG | 51317 |
rs529698499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45999617 | TGTATAATTTAGGAG[A/G]AGCTGAATATTTAAT | 51317 |
rs529714237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46041186 | TTTCAAATACAGAAG[C/T]GGAAATAGTCACCTT | 51317 |
rs529720982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46056386 | CCAATTATGTCTGGG[C/T]TAAATATGGAGGTGA | 51317 |
rs529733874 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46004378 | ACTGTAAAAAACTTG[G/T]ACTTTTGACCAAAGG | 51317 |
rs529743298 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46091130 | CCAGTCCCCAAAAGG[A/G]AGAGAGACACCACAA | 51317 |
rs529749434 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46040426 | TAACTTAGCAATCTA[A/C/T]TTATAAGTAGAAGAG | 51317 |
rs529801313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46100348 | GGTCCCATTAGGCAC[C/T]CTATTTTACTTCCAC | 51317 |
rs529801869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46064473 | CAAACCCTGCTGATT[C/T]ACACAAACATTTGCT | 51317 |
rs529842962 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46099936 | ACAATTTACATTTTT[A/T]AAAAAATCTTTGTAG | 51317 |
rs529848945 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46067129 | TGCACCTTGATTCAA[A/T]CACATTTGTTTTCAA | 51317 |
rs529904849 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45938344 | AAAGGTAAGAAAAAG[G/T]ACAAAAAAGGTAAAA | 51317 |
rs529930056 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46008224 | CTAGACTAATCCATA[A/C]TGTTCAGATGATAAC | 51317 |
rs529939440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45999107 | GCTGGGATTACAGGC[A/G]TGAGCCACTGTGCCC | 51317 |
rs529944822 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45964450 | CAGGCAGCATCTGAA[C/G]AGCCTCTCTGAATCA | 51317 |
rs529954369 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46073009 | GTGGGGAGTGAGAAT[C/G]AGAGTGAATCCTGTT | 51317 |
rs529959282 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PHF21A | GRCh38.p7 | 11:46055712 | ATCTCTTTATATAAA[C/T]GCCCCAACAATTTAC | 51317 |
rs529960462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45954317 | TTTTTATATTATAGG[C/T]CAAGCTCCAGCTCAC | 51317 |
rs529967221 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46107151 | CTCATCCTTTTAAAA[A/T]TTTCAAATTTCCTAT | 51317 |
rs529973700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45947258 | CTTGTCTTCTAGGGG[C/T]AAGGTCATTGCTTCT | 51317 |
rs529985493 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46064042 | CTCCCCCAATTTCAC[C/T]TGATTATTTTCCTTC | 51317 |
rs530007690 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46021140 | TCATAGCTCACTGCA[A/G]CCTTGACCTTCTGAG | 51317 |
rs530028099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46030102 | ACGGTCTTTGGACAA[A/G]GAATCAACGCTAAAC | 51317 |
rs530035843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45946529 | GCTGGGACAACAGGC[A/G]TGTGCCCAGCTAATT | 51317 |
rs530069145 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45980144 | ACATTATTGGTAATA[A/T]GAAACTGATGGTGTA | 51317 |
rs530084750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46080515 | GATACTTAGAGGAAT[A/G]ATTATATTAATATAC | 51317 |
rs530119776 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PHF21A | GRCh38.p7 | 11:46065330 | ATAAAAAGAGATATT[C/T]AATAAGAAATGGTCC | 51317 |
rs530144173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45963277 | ATACAAAAATTAGCC[A/G]GGTGAGATGGCGGGC | 51317 |
rs530182336 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46021765 | TTTGTTGCCCAGGCT[G/T]GTCTTGAACTCCTGG | 51317 |
rs530187036 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45958684 | ACTTTGGGAAGCCAA[A/G]GTCGGGGGATCACTT | 51317 |
rs530199572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46081210 | TGCCAACCATGGGAC[C/T]TCCAAATACACAAGG | 51317 |
rs530212763 | in-del | -/T | 0.00517822 | 0.0506191 | intron-variant | PHF21A | GRCh38.p7 | 11:46074231 | AAATATTGAAAAAAA[-/T]GATTACAGAAAAATG | 51317 |
rs530227984 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45936098 | GCCTGGGTGACATGG[A/C/T]GAAACCTGTCTCCAC | 51317 |
rs530235796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45997566 | TCAGATTTCTCCTCT[A/G]CCTAATAACATTTTT | 51317 |
rs530256720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46053901 | ATGTGATGATTACAA[C/T]CCCTCCAATGAGATT | 51317 |
rs530261654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46030609 | CACCTTGAACACAAA[A/G]TTCAAAAAGATTCTT | 51317 |
rs530264909 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | PHF21A | GRCh38.p7 | 11:46052036 | CAAAGGAATAGTCAA[C/T]AGTCAAGGTTGAGAT | 51317 |
rs530286077 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46070175 | ACTAGTTATAGGAGG[A/G]ACAGAAACTTCTTTC | 51317 |
rs530288199 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46030829 | TGTGTGCGTGTGTGT[A/G]CGTGTGTGTGTGTGT | 51317 |
rs530304787 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46054642 | AGATCTTATTACTCT[A/G]CAACTGTTGAGAAAA | 51317 |
rs530308312 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45989080 | GGAGGGTGCAAGTTC[C/G]TCACAAGTGCAGCCT | 51317 |
rs530315772 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46045294 | TCCCTATGAAAGATC[A/G]TAAGCATTAGCACAC | 51317 |
rs530316773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46097563 | TAATCAGAATTGTTC[C/T]GCTCCCCAACTTTTA | 51317 |
rs530340466 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:45941826 | AGGAAGCACTCTGGC[-/A]ATACCAACTGCAATT | 51317 |
rs530356616 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45985450 | TTATGGACAAACACA[C/T]AGAAGAGAAACTCAA | 51317 |
rs530391915 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46038475 | ACCTCCATGTGCTAC[A/G]TACTATTCTAGGTTC | 51317 |
rs530408755 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46088798 | ATATATCTAGAAGAC[A/T]GTAGGCTTTTCTGTT | 51317 |
rs530414073 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46046159 | TGTTTTCAAGAGTGT[C/T]CCTGAGCTTATGCAC | 51317 |
rs530423968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46055573 | TTGACCTTTCCAATT[C/T]CCTAGAGCAGTCAAT | 51317 |
rs530429194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46037777 | ACTTGAACAATACTT[A/G]AAAATTTTAGCAACA | 51317 |
rs530449083 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46097145 | TTGCAACAGCCTCCT[A/G]ACTGGCCTCCCCAAT | 51317 |
rs530449496 | in-del | -/ATCT | 0.433442 | 0.16985 | intron-variant | PHF21A | GRCh38.p7 | 11:46015899 | GTTTTACAGTCATCT[-/ATCT]ATCTATCTATCTATC | 51317 |
rs530451915 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46023812 | AATACAAAAATTAGC[C/T]AGGTGTGGTGGCGGG | 51317 |
rs530475936 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930907 | CAGGTGGTCACAGGC[A/C]CCCCCCCCTCCCCGC | 51317 |
rs530481323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45999046 | TGGCCAGGCTGGTCT[C/T]AAACTCCTGAGCTCA | 51317 |
rs530488450 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46039336 | TTCATAGAACTGGTA[A/C]TTTTTTCTTGTCTGC | 51317 |
rs530519706 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:45999365 | TTGCAGAAATGGAGT[A/G]AGGCAAGTTTCCCTG | 51317 |
rs530522816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45998634 | TCTCCTGCCTCAGCC[C/T]CCCGAGTAGCTGGGA | 51317 |
rs530530096 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46007460 | CTGGGTTTACAGGTG[C/T]CCACGACCATGTCCA | 51317 |
rs530544626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46106309 | ATCTCCCCTGAGCAC[A/G]AAAGGGTGGGGGGGA | 51317 |
rs530562934 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46064093 | GTAAGTTCATTTGTG[C/T]TTCTTGACTCCACAG | 51317 |
rs530565120 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45971980 | GAGGTAGTTACCCTG[A/G]AGGCAATGAGTCCCA | 51317 |
rs530579870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46072143 | TACAGATACAGATAT[A/G]CTACTGTAATAGAAA | 51317 |
rs530597403 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45990416 | CGAATGCACCACCAC[A/G]CCCGGCTAATTTTTT | 51317 |
rs530623615 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46060445 | TTAGCACATACTCAT[A/G]TAAAATTATGTTATA | 51317 |
rs530636195 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46021668 | TGCCTCAGCCTCTCA[A/C]GTCTCTGAGACTATA | 51317 |
rs530712436 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46063730 | TATAAAAAGGAATAC[C/T]AGAAATTTAAAGAGT | 51317 |
rs530740902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46013906 | GTCAGTGAATGAGTG[A/G]TTAGTAAATGTGAAA | 51317 |
rs530753109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45962424 | ATACTGGAAATGAAA[C/T]ATAAATAGAAAACAA | 51317 |
rs530773776 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46080350 | TTTTTGTAGAGACAG[C/G]GTCTTGTTATGTTGC | 51317 |
rs530779897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46114781 | GCACATGGTTAACAA[C/T]ACTTGGATCTGCAGC | 51317 |
rs530781360 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46071459 | CACTTAGGTAAAATG[A/C]CCTATAATAATATGG | 51317 |
rs530794580 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46051211 | AAGTATGTGGTTTCT[C/T]ATACTAGATCTAATC | 51317 |
rs530806880 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45988463 | CACTTGTATATAACT[A/G]AACACTGGCATTTTT | 51317 |
rs530869620 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46021260 | GAGATGGGGGTCTCA[A/C]TCTGTTGCCCAGGCT | 51317 |
rs530869714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46029878 | AAGGCATAGAAGAAG[A/G]TAAGAATGTGAATCC | 51317 |
rs530883971 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930094 | ATTCAGCCCTTTAGA[C/T]AAATAAGAAGGACCA | 51317 |
rs530896262 | snp | A/T | | | downstream-variant-500B, utr-variant-3-prime | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45929086 | TTTCATAATTAAAGT[A/T]TTAAAACATCTTTTT | 51317 |
rs530898418 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | PHF21A | GRCh38.p7 | 11:46088582 | CACTGTGTGACTACT[C/G]TCATCCCCAGGGTTC | 51317 |
rs530898556 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45971405 | ATTAGGACACTAAAT[A/C]TAAACTAAATAATAA | 51317 |
rs530917661 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45929578 | CCGTCCCATCCCGCC[C/T]GACTGCAGCTCACCC | 51317 |
rs530953556 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46029177 | TCTCATAATCTTTGG[C/T]CAATTTTTTTGCATT | 51317 |
rs530954150 | in-del | -/ACAAACTA | | | intron-variant | PHF21A | GRCh38.p7 | 11:46049190 | AACAGCTTTTTACAC[-/ACAAACTA]ACAAACTAATGTTGT | 51317 |
rs530993650 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45943959 | TCTACAGAAGAACTG[G/T]CTATCTTTTTAAAAA | 51317 |
rs531011670 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PHF21A | GRCh38.p7 | 11:46079545 | GCCCCACACAAAACC[A/G]GCCTGTTCATACACA | 51317 |
rs531018859 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45982746 | GCATCAGCAGCCAGA[A/G]AAAGGAACCCTAAGA | 51317 |
rs531034037 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45935874 | CAACCCAGTGCAGAG[A/G]ATCTGCCCACCTGGA | 51317 |
rs531049216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45952085 | GGTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC | 51317 |
rs531077760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46045248 | CTTCACTATGTACTG[C/T]CCTGGTCTACCATGT | 51317 |
rs531084545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45987755 | AATTTGTAAATTAAG[C/T]TCCAATAGAGCAAAA | 51317 |
rs531108834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45997286 | GCTGTATGTTTTTAT[A/G]ACACTTATCACTAGT | 51317 |
rs531124993 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46053116 | GATTACATTTTCAAT[G/T]CAAAATTTGTAATTA | 51317 |
rs531143684 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46020634 | TTATGAAATTTCTCA[A/G]ATATGAACATGACCC | 51317 |
rs531163745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46061449 | AGGCTTGTATTATTA[C/T]ATAAATAACATTAAT | 51317 |
rs531177421 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45943242 | ATCCTCCCACCTCAG[A/C]CTTGCAAGCAGCTGT | 51317 |
rs531180955 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:45935949 | TGGGTCTGGCTTTAC[A/G]TAAATGAGATACCAC | 51317 |
rs531184823 | snp | A/C | 0.000186431 | 0.009653 | downstream-variant-500B, utr-variant-3-prime, missense | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45928897 | CAGACACCAGGGCAA[A/C]CTGCCCTCCGCCATC | 51317 |
rs531200255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46036939 | TAGTCTTGAACTCCT[A/G]GCCTCAGGCAATCCT | 51317 |
rs531238239 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46044334 | TCATGCAAGGTAAAA[G/T]AAGTAATTAGAAATT | 51317 |
rs531241045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46053616 | TTAATCAGTGTTTCA[C/T]ACAGGCTGAACATTA | 51317 |
rs531241855 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45984304 | CCAGAACTGCTAGTA[A/C]CGCCCACTTCAATCC | 51317 |
rs531249659 | snp | C/T | 0.00026775 | 0.0115673 | intron-variant | PHF21A | GRCh38.p7 | 11:45935569 | CCACACGTACTGTTA[C/T]GTATATTGGAAAGGC | 51317 |
rs531257557 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46017593 | GGGGGAAAAAAAAAA[A/C]ACACCTCCCTCATCT | 51317 |
rs531258973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46026031 | ATGTCCTTTAAGTAA[A/G]AGAGAGTCTCAGATC | 51317 |
rs531309182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45975622 | TTTGCATTATGCCAT[C/T]AAAAATTAGAGGGCT | 51317 |
rs531339430 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46070933 | TGGGGAAAATCACTT[A/T]TTATCAATATATGCT | 51317 |
rs531344503 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46025316 | AAACTTACTATGTCC[A/C]TTTCACACAATATGA | 51317 |
rs531412619 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:46075672 | CGCATAAGAATAGGA[A/G]GGAAGAATATAAAGC | 51317 |
rs531413045 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46085579 | TTCTTTTCTTCTTTG[C/T]ACCTATAAAGCTTGT | 51317 |
rs531445088 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45962003 | GACAGGGGAAGGACA[C/T]GTGAGACCACTGCTG | 51317 |
rs531470811 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46032456 | TCCTTTTCTTAACAA[G/T]TGCACTCACAAATAC | 51317 |
rs531477737 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46106451 | CTGATAAGTTAACGG[A/C]ATCTGTTCCTTTCAG | 51317 |
rs531480289 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45992846 | AAAACAGCTTAAAGT[A/G]CCTTACATATAATTT | 51317 |
rs531493514 | in-del | -/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45967442 | CCATGATTTGGGCTT[-/C]CCTAAGTGGGGTGAC | 51317 |
rs531512662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45940000 | TGCACAAGAAGCAAT[A/G]ATAGAGAGGAATGTG | 51317 |
rs531524195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45940668 | ATTATTAAAATCAGG[C/T]TGAGGGCTACTCTTT | 51317 |
rs531535576 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46000961 | AATAAATAAATTTAT[A/C]TGTCACTTTTTCATT | 51317 |
rs531536679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46100681 | AACTTTCACTGACTA[C/T]GCTTCCCCATGCATT | 51317 |
rs531558125 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46074465 | TCTTTTGGCGGGAGG[C/G]GGGAAGGCATATAGC | 51317 |
rs531559358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46065480 | ATGAATATGGGTCCT[A/G]ATAGTGTTGCTGAGC | 51317 |
rs531574630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46057454 | GGCTTAATTTTCCCA[A/G]TGAACCCAGGCTGGT | 51317 |
rs531576161 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45948764 | CTCAGAGAACAACAA[C/G]AAAACTATTTTCAAA | 51317 |
rs531624612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46101360 | TTCCTTTGAGTATAC[C/T]AATGTATCTAACTGT | 51317 |
rs531627480 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46082313 | TTGTCCCACTATTTC[A/G]TCAAATGTATGTTCT | 51317 |
rs531674788 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46026392 | CTGACAATGAATAGG[A/G]CTTAGAATATCATTC | 51317 |
rs531688781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46117492 | TTAAGTACATCAACC[A/G]TATGTATTTATAAAG | 51317 |
rs531694581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45957273 | CTTGAACAACACTAT[A/G]CACCAATTAGACCTG | 51317 |
rs531701989 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46000045 | TCTAGGGGAGATTCT[A/C]ATTTTTCGATTGACT | 51317 |
rs531709011 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45961251 | CTCTGCACAAACCTA[A/G]AATGAAGTTAATCAA | 51317 |
rs531738445 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46008552 | AAGAGTCTGCTTTGA[C/T]TGGCTGTCAAATTTA | 51317 |
rs531752903 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46083231 | CGTGCATAGGGCCAA[C/T]TCTGCAGCGGAACAA | 51317 |
rs531754958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46081610 | GGGGTAGGACAGGAC[A/G]AGCTGGCCAACTTAC | 51317 |
rs531756268 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46091073 | AGGTAGTAAATGCAA[C/G]GATTAACTAGTTCAA | 51317 |
rs531758057 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45974936 | GCATGGCAAATACTG[A/C]CAATAGCAAAATCCT | 51317 |
rs531787324 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45973046 | TCACACCATTGCACT[C/G]CAGCCTGGGCGACAA | 51317 |
rs531829240 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46109216 | TGTTACCTATGTGAT[C/T]CGAGGGAAACCTCTA | 51317 |
rs531847142 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:45981511 | CATAAAGCATATAAT[A/T]ACTATTTGGGGCCAT | 51317 |
rs531877636 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46027732 | CCCATATGGAAAAGC[C/T]ACTGTCCCAGGAATC | 51317 |
rs531886764 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45979011 | TGAATAGTGCAAATA[C/T]AGCACTCTTCTTTTT | 51317 |
rs531892898 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45964624 | TCTTTCTCATCACTA[C/G]TCGTTTTTCAAATAG | 51317 |
rs531908194 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45982397 | GTAAATATTTTTTTT[A/T]AAATGATGCAGAGTT | 51317 |
rs531937697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46099897 | AACCCTGACTTTAGG[C/T]CTAAAAACTAAAAAT | 51317 |
rs532027891 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46065098 | ACTTTCTTGAATATC[C/T]ATTCTTCTCCACCCT | 51317 |
rs532048941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46033333 | GCAGTGGTGCAATCA[C/T]GGCTCACTGCAGCCT | 51317 |
rs532064630 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46100126 | CCTCAATCACGCTGA[G/T]AAGTAAGTAGTCCTA | 51317 |
rs532070470 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46031682 | CGCTCCGAGGCAGGT[C/G]AAATCAAAAAGGTTT | 51317 |
rs532082144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46022870 | TCACTGCAACCTCCA[C/T]CTCCTGAGTAGCTGG | 51317 |
rs532085244 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45983419 | CCACTCAGAAATGAA[A/T]TGTCCCTTACTCCTT | 51317 |
rs532090196 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | PHF21A | GRCh38.p7 | 11:46084058 | GACTCTTGGACAAAA[G/T]TGTCTTAAAGATTAT | 51317 |
rs532104149 | snp | A/C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46043913 | CAGTAAAAGATGGAT[A/C/T]GCAGCAACTGCTTTA | 51317 |
rs532111422 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46068147 | AGGTATCAGTGCTAA[C/T]GAGCTTGAATGCCTT | 51317 |
rs532113922 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46041309 | AAAGATAAGTCATTA[A/C]CAAATGAGATCTTAT | 51317 |
rs532114653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46091848 | ACACACCCACTGGGC[C/T]TGGCTGGGAATCTGA | 51317 |
rs532117465 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46045782 | CTGTGAGTTTCTTAA[C/T]CCCTTTCTGCTCCAA | 51317 |
rs532133035 | snp | A/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45932436 | CTTTTCTGAGGAGAG[A/T]GAAGGGTGGGGAGCT | 51317 |
rs532140175 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PHF21A | GRCh38.p7 | 11:45999387 | GTTTCCCTGCTAGTG[A/G]TTGATTATAGGTCTC | 51317 |
rs532142078 | in-del | -/C | 0.0100141 | 0.0700482 | intron-variant | PHF21A | GRCh38.p7 | 11:46034222 | ATATTAGTGCCCCCA[-/C]CCCCCCCTTGCATAC | 51317 |
rs532148199 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46001300 | CAGGGGGGCTGGAAA[C/T]GGGGCTCTAAGATGT | 51317 |
rs532148647 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46103521 | TCTCCTCAGAAATGA[A/G]ATACAATGTTTTAGG | 51317 |
rs532178897 | in-del | -/TA | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46054273 | GTAACCCTTGAAAAT[-/TA]TATCACATAAAGTTT | 51317 |
rs532182262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45963485 | CTAAACTGTTAATAG[C/T]AATTAACTCCTGGGG | 51317 |
rs532234251 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45974803 | TTAGCTAGTTAACAG[G/T]GTCTAAGTATGATCA | 51317 |
rs532271903 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46000875 | CAGTGAGCCAAGATC[A/G/T]CACCATTGCACTCCA | 51317 |
rs532272494 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46106554 | CAAAGTTTGGTCTTC[A/G]AGATATGATGATTTC | 51317 |
rs532290289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46117408 | ATGCAGTTACTGTTA[C/T]ATCAACAATGACCTA | 51317 |
rs532310616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46048622 | TAAAAATACAAAAAT[C/T]AGCCGGGCATGGTGG | 51317 |
rs532311990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45947576 | TGCTCTCTTGTTTAC[C/T]CACAAAAGGCATATC | 51317 |
rs532314776 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45941177 | GATCTTGGCTTACTG[C/T]AGCCTCGACCTCCCA | 51317 |
rs532319976 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46031985 | GTTCTCTTCCACACT[A/G]ACATGAAAACCACAG | 51317 |
rs532336930 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46107994 | ACTAATTCCTATGTA[C/G]GGTATCTTTACGCTG | 51317 |
rs532341235 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:45964606 | TTTTCTTTGCCAAAT[C/T]CTTCTTTCTCATCAC | 51317 |
rs532360231 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46073090 | TCCCAGCACTTTGGG[A/G]GGCCGAGGTGGGAGG | 51317 |
rs532399102 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PHF21A | GRCh38.p7 | 11:45972981 | TACTCGGGAGGCTGA[A/G]GCAGGGGAATCACTT | 51317 |
rs532399409 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45931707 | CTCTGGCCATTCCCA[A/G]GGCCTGGAGTGGGCT | 51317 |
rs532404297 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46049233 | GAGAAAGTAATACAG[A/C]ACTGTCAGAGCCAGG | 51317 |
rs532433721 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46109048 | GCCTCAAAATGATAC[A/G]CTGTAGCTGTGGCCA | 51317 |
rs532444479 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46100016 | TCTTTTTATCAGTAC[G/T]TTGAAATGTCAATGA | 51317 |
rs532446895 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46081399 | TTCAATGAAAAAAGC[G/T]CTTGATTTTCCTTTT | 51317 |
rs532473580 | snp | C/T | 5.00113e-05 | 0.00500031 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45965380 | GTCTGGTCCCTGGAG[C/T]AGCTATCACAATGCT | 51317 |
rs532496011 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46082562 | TGTATAAAGGATGAA[A/T]ATAAAAGCTATTAAT | 51317 |
rs532505310 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45955528 | TCTTGGAGTCTCTTA[A/C]TTCCATTTCTAAGGC | 51317 |
rs532543065 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46098714 | GGACTAAAACTCTTG[A/T]CATTAACAACAAAAA | 51317 |
rs532579399 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46097663 | ACACTAGGGTCCAGA[A/T]AAAGACTCACTGATT | 51317 |
rs532597136 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930323 | ACGCTGCCTGTTGGG[C/G]CTGAGCCAAGCAGCA | 51317 |
rs532600324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46015411 | TTAGCCATAAATTCT[C/T]TGCCTAGGCCAATTT | 51317 |
rs532653900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46089981 | CATCAGTGCTCAGCC[C/T]AATATACAGTTTCTA | 51317 |
rs532684289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46023262 | TCCATAAGGCAGGCC[A/G]GGATCTGGCAGAGAG | 51317 |
rs532700460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46021331 | CCTTCCAAAGTGCTG[A/G]GATTACAGGGATAAG | 51317 |
rs532711125 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45990161 | ATACACATGTATGCA[C/T]CCACTAACACAAACA | 51317 |
rs532734007 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46047123 | TAGGGACAAATTAAT[A/G]AGCAATTGGTAGAGT | 51317 |
rs532755529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46078229 | ACACAATAGTTAGAC[C/T]TGAGTTCTCAATTTG | 51317 |
rs532781361 | in-del | -/G | 0.00279162 | 0.0372561 | intron-variant | PHF21A | GRCh38.p7 | 11:45990714 | GTCCCTTGATTTGTT[-/G]TTTTTTTTTTAAAGA | 51317 |
rs532792105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45968786 | AATACAAAAATTAGC[C/T]GGGCGTGGTGGCACA | 51317 |
rs532832824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45981309 | GAGAATTGCTTGAAC[C/T]TAGGAGATGGAGGTT | 51317 |
rs532850031 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | PHF21A | GRCh38.p7 | 11:46021071 | TTCTTTAAAAAAAAA[A/G]AAAAGAGAGACAAGG | 51317 |
rs532855122 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:45937733 | TGACCTGCCCGCCTT[A/G]GCCTCCCAAAGTGCT | 51317 |
rs532858778 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46122337 | AATGCAACATGCAAT[A/C]CCCGGCCGCCGCTCG | 51317 |
rs532862001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46039112 | GACAGACAACTCTAA[A/G]GACTTGACTTTTATT | 51317 |
rs532865123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45961312 | ATCAAAGGTAGGCAG[A/G]TGCAAATAAATGTCC | 51317 |
rs532878302 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930873 | GGCTGGGGTGGGGCA[A/G]TGTCACGAGCGTATG | 51317 |
rs532893124 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:45993125 | AGTACTCTGATTTTT[C/T]AAAATCATTTAATTT | 51317 |
rs532902947 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46069122 | CCTCTCGATCTTCAG[A/C]ACTTTCATACTTGCA | 51317 |
rs532908605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46070306 | CATCTAATATTATAT[C/T]GAAAAGATCTGTAAG | 51317 |
rs532917093 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45960529 | CTGGTGATTGCCAGC[A/G]GCAGAGGGCAAAAGT | 51317 |
rs532926601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45975972 | CCCTCATACATTAAA[C/T]ATATGTATTTAATAT | 51317 |
rs532930534 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46042388 | GTATGTGTGATAGTG[C/T]AACTCCGGAAAGTTC | 51317 |
rs532931482 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46094718 | AATAATAATTATTTC[A/G]TAGAAGTCTCTACTA | 51317 |
rs532932922 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46085964 | TCCAAAAGTGCAAAA[A/T]TCCTTTAAATTCACA | 51317 |
rs532956528 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45986224 | GACTTTAGACCTTTT[A/G]TTTGCTAGCCTGATT | 51317 |
rs532969305 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46093872 | GAATGACTTTCTGGA[A/T]CTGTTTTCATCCAAG | 51317 |
rs532974449 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46019026 | TTGGTCAAAATAAGG[C/G]AAGAAAAAGAAAGGG | 51317 |
rs533039062 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46086754 | TTCGTACTTCATTCT[A/C]CTGACAGTAACATAA | 51317 |
rs533047285 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45968099 | AAAATGGATACTCCA[A/T]GTAAAGTGCCTAGCA | 51317 |
rs533047646 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45951388 | AGCCACTTGAGAACA[C/T]AGAAATGTCATTTAC | 51317 |
rs533074220 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46011540 | GAAGTAAGAAGATTG[A/G]CAATTTCTAAGATAC | 51317 |
rs533076554 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45946577 | GGACGGGGTTTCATC[A/G]TGTTAGCCAGGATGG | 51317 |
rs533098907 | snp | A/G/T | 0.00557734 | 0.0525397 | intron-variant | PHF21A | GRCh38.p7 | 11:45976600 | TAATCCCAACACTGT[A/G/T]GGAGACCGAGATGGG | 51317 |
rs533106499 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46006744 | TGAACTGTCTTAAAC[A/G]CCTATTAGAATGTGA | 51317 |
rs533119019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46035902 | TGGACTTGGTCCTAA[A/G]AGCAAAGAGAAGACA | 51317 |
rs533133683 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45940992 | TATCTGGTGTATATA[C/G]CCTATAATTTTTGGT | 51317 |
rs533135133 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45936285 | CCTTGTCTCAAAAAA[C/T]AAATGAATAATAATA | 51317 |
rs533139408 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PHF21A | GRCh38.p7 | 11:46034888 | TTCCTCAAGTATTTT[C/T]AACATGCCAGAGAAC | 51317 |
rs533150659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45949755 | GTCCTGATTTTTAGA[C/T]TGCTGTATATATAGG | 51317 |
rs533163866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45985238 | ACCAATATTCATCAA[C/T]GCTGAGGATGCAGGA | 51317 |
rs533187631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46058772 | AAGCAGGCTTATTAC[A/G]TTCTCTTTACAAAAT | 51317 |
rs533216507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46027113 | CAGCAATCTAGCAAC[A/G]AGCCTCCCAGATTAT | 51317 |
rs533259296 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46050831 | TGTCCAGCAACTGAG[G/T]ATGTGTGCAGGACTA | 51317 |
rs533264109 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45941746 | TTACTATAAACCAGA[C/T]GGTAGGTAAGTTGAA | 51317 |
rs533264340 | in-del | -/G | 0.00835141 | 0.0640778 | intron-variant | PHF21A | GRCh38.p7 | 11:46105860 | CTGAATATCTTGATA[-/G]GTGTATTTAAAACAA | 51317 |
rs533266082 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45933621 | CCCTGCTCCCCACCC[A/C]AGAAAACAGAAACAA | 51317 |
rs533289677 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45942395 | ATCAACTGTCCCCTA[A/G]CATTTGTGTACCACC | 51317 |
rs533301532 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45979039 | TTTTTTTTTTTGAGA[C/T]GGAGTTTTGCTCTGT | 51317 |
rs533303486 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46089425 | GAATCAATACAAATG[A/C]CAACATTAAAAAACA | 51317 |
rs533328203 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46038094 | GCCTCCCTGTATTGA[C/G]TTTACTTGTATACTC | 51317 |
rs533328383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45957836 | ACAGACTCAACAAAA[C/T]CAAAAGGTGAATCTT | 51317 |
rs533333166 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46025207 | AAAAAAAAACAACTT[G/T]TCTCCATCTCCCAAC | 51317 |
rs533376356 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46016726 | ACATGGGGAGACTAG[G/T]TCTTGCTGATTTTAT | 51317 |
rs533389180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46001855 | GGTCTTTGGTTTCTA[C/T]GACAACCCAGATGGG | 51317 |
rs533395868 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46119582 | CTTAGAAATCACTCT[A/C]GGCACATCTGCACCC | 51317 |
rs533401721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45949312 | ACAATCAGGGTGCTG[C/T]TCTTCAGCAGGTTTT | 51317 |
rs533410174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46074723 | GGCCAGGCTAGTCTC[A/G]AACCCCTGACCTCAG | 51317 |
rs533433118 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46042804 | CTTCTTGCTATGTCC[A/T]CACAGCAAGAAGGTG | 51317 |
rs533460052 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46102044 | TGTATTTTTAGTAGA[G/T]ACAGGGTTTCATCAT | 51317 |
rs533464663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45993894 | AGTGCCTATCTGAGA[C/T]GAATTTCCTAGAAAC | 51317 |
rs533499006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46111121 | CAACTATGTGGGGGG[A/G]GAGGCTAGTATTATT | 51317 |
rs533502077 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45992997 | GAAAACTGAAAACTA[C/T]CTTGCTGAAGCTATC | 51317 |
rs533519280 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:45968315 | TGCCTGCTGCTCCTA[C/G]GATAAGGCCCAGGTT | 51317 |
rs533532518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45967090 | TGACCCTTTCCTGGC[C/T]GGGCACAGTGGCTCA | 51317 |
rs533535629 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46017704 | AAAGATTACATAAAT[C/G]AAATGCAAATGATTT | 51317 |
rs533595875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45975442 | GAATTTAAGGGATTA[C/T]TACTATGGGATCTAA | 51317 |
rs533604360 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46002119 | TTACATAAGTAAATG[C/G]TTTCATTAAAATTTA | 51317 |
rs533636673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46010294 | ATTTTTAAAATGTCA[A/G]CATTTTGTAAATATA | 51317 |
rs533640819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46119807 | AGACCAAAGAGAGGA[C/T]GACGAGAAGTGTTGG | 51317 |
rs533660291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46118654 | TTCAGACATTTTTAA[C/T]GACCCCCTAAAATAA | 51317 |
rs533684608 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PHF21A | GRCh38.p7 | 11:45958387 | GAGCAACATGACAAA[A/G]CCTGGTCTCAAAAAA | 51317 |
rs533690260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46010443 | ATTTGTCTAAAATTA[C/T]ACAGTTAAGTGGCAA | 51317 |
rs533696453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45974994 | CATTGTTGTCTGCCT[A/G]CCAAATATGAAGTAT | 51317 |
rs533728135 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46067795 | CACAGTCCTTGCCTG[C/T]GAGGATCTTACAAAT | 51317 |
rs533729128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46017565 | TAAGTTACAGTTCAG[A/G]ATTTGCCCTTAAGGG | 51317 |
rs533734334 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45949104 | GTTTTATTGTATGTA[C/T]TTGGCTCTCAGAGAC | 51317 |
rs533738865 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46110374 | TGGCCTGGGGCATTT[C/T]ATTAAAAAAGAAAAC | 51317 |
rs533753476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45974255 | AGATCTTTACCCCTA[C/T]TCTGGTGCTTCTTCT | 51317 |
rs533755426 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | PHF21A | GRCh38.p7 | 11:45983507 | GTGAAAAAAAAAAAT[A/T]TTTAAATCAAGATTT | 51317 |
rs533793920 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45965824 | CATAGCTTTTGATTC[G/T]AAACCCTGAGCTCCC | 51317 |
rs533813683 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45958061 | CACATTACCAAAATT[G/T]ACTCAAGATAAAGAA | 51317 |
rs533816475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46025508 | TTAATCATGTATAGC[C/T]CTGGACTACAAAAGA | 51317 |
rs533817990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46075753 | CATATCTCTTCCACA[C/T]AATTCTCAAAGTTTA | 51317 |
rs533830338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46085046 | TTCTCGGAGGTTAAC[A/G]AATGCCAGGGTAGTT | 51317 |
rs533882035 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46071332 | ACCTAACCAAACCTG[A/C]AGCCTGAAAGGCAAG | 51317 |
rs533889802 | snp | A/C | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46119105 | TCCCAGAGTGCACAA[A/C]TGCTTTAAAAAAAAA | 51317 |
rs533898058 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PHF21A | GRCh38.p7 | 11:46012586 | AGATAAAAGTAGCTA[C/T]CTCAAAGGGCTGTGA | 51317 |
rs533941036 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46088122 | CTGGGAGGCAGTTTA[C/T]AGCATCAAAAGAATT | 51317 |
rs533955375 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46108375 | AAAGCATGAGGTACA[A/C]TCAATCTAAGGCATT | 51317 |
rs533961333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46084402 | TATCTGATTCTCTAA[C/T]GCAGGGCAAGAAATT | 51317 |
rs533961871 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | PHF21A | GRCh38.p7 | 11:46035078 | ATTCCTGAGGGAATA[C/G]TGTTCACCTATTCCC | 51317 |
rs533979175 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PHF21A | GRCh38.p7 | 11:45938655 | TTAGGCACAATAAGA[A/G]ATTAACAACAGTGAC | 51317 |
rs533979235 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45947982 | TGTAGTCCTGCCTAA[A/G]GCAGACAAAGGGTCA | 51317 |
rs533997446 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PHF21A | GRCh38.p7 | 11:45933082 | ATAAATATAGAAAAG[A/G]GATGGAGCTTGTTTT | 51317 |
rs534000702 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46092006 | CAGAAACACAAATGC[A/G]TTTGAAGTATAGCTA | 51317 |
rs534007203 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | PHF21A, LOC105376661 | GRCh38.p7 | 11:46123320 | TTTTACTTTCGTGAC[C/T]TGCAAAATTAAGTTT | 51317 |
rs534008414 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:45982992 | CTCCTAATCACTGCC[C/T]AGCTAAAGTACACTA | 51317 |
rs534011416 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46041558 | CTTCTTTCTGGGGTA[C/G]TGTGATTTATTAAGT | 51317 |
rs534011454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46032024 | GCTGATAATTTAAAA[C/T]ACAGTCAAAGCCCAA | 51317 |
rs534019863 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46107896 | AGTTATCAGCATAGC[A/G]TTTGGTAGTGGTTGA | 51317 |
rs534034226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46091557 | TACTATCAGACATGA[A/G]GCTAACTAATCCAAT | 51317 |
rs534063393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46074880 | AGCTTTTGAACTTTA[C/T]AGCTGTGCTTCCTTC | 51317 |
rs534068853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46017009 | GGAGTCTCACTCTGT[C/T]ACCCAGGCTGGAGTG | 51317 |
rs534095031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46064921 | GCAGGCTGCTAGCTA[A/G]GGTGGCAAAGGGAGA | 51317 |
rs534101738 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46024628 | ACAATGGTGAAACCC[C/T]ATCTCTACTAAAAAT | 51317 |
rs534130185 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46073201 | GGCGTGGTGGCGGGC[A/G]CCTGTAGTCCCAGCT | 51317 |
rs534154048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46048727 | GGGAGTCAAGATGGC[A/G]CCACTGCACTCCAGC | 51317 |
rs534185456 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:45999435 | ATGTACCCAGTGAAA[C/T]AGCACATAGTATATA | 51317 |
rs534207989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46056108 | GCTTCTCTGTTTCCT[A/G]TCTTAAAGTAACAAA | 51317 |
rs534296596 | snp | G/T | 3.35954e-05 | 0.00409836 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45935722 | ATTTAAGTAACTTCT[G/T]TTTCTCTTCTTCTTT | 51317 |
rs534315273 | snp | A/G | | | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46084481 | TAAAGAACACTTCAA[A/G]TAACTAAGAAATGAA | 51317 |
rs534315576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46044612 | TTTTGCTTCTGCAAC[A/G]GTTATCCAAACTCTT | 51317 |
rs534330772 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46087254 | ACTATCAAACAAAAT[C/G]CTCAGGAAAAGAAAA | 51317 |
rs534344039 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45996567 | TCCTGGAGTTTTTAA[C/T]GCAGTGCCAGGAATG | 51317 |
rs534351955 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46117811 | CAGTGCTCTGTACCA[A/C]GGGCCAGAATCCTTA | 51317 |
rs534353737 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46053209 | CTAGATCACATCTCT[A/C]ATGGATAGCAGAATA | 51317 |
rs534356772 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PHF21A | GRCh38.p7 | 11:45935097 | TCTTTCCCACTTGGA[C/G]AGGCCGGGCTGGGCA | 51317 |
rs534373656 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46014990 | GTCTCAAAAAAAAAA[A/T]AAAATAAAAATAAAA | 51317 |
rs534374750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45955682 | ATATAAATAATACCA[A/G]AAGGATCCAAAAACA | 51317 |
rs534406017 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46068794 | TCCATTTGCCAGCAC[C/T]AAAAATACGTTATTA | 51317 |
rs534406339 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45984229 | GGAGAAAAAATTAAT[A/C]ACTTATCATCTTTTC | 51317 |
rs534418927 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46030156 | TCTGGAGAATATCTT[C/G]CTAATACATTAAAAG | 51317 |
rs534432326 | snp | A/G | 0.00557542 | 0.0525036 | downstream-variant-500B | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45929158 | GGCGTCAGTGCACAA[A/G]GGAGGTGCTACATCC | 51317 |
rs534438009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45964843 | TGCTTTTTGGAAATT[C/T]TAATTTTTTTTGTTT | 51317 |
rs534444897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46096495 | AGTTGTTAAATCCAA[C/T]AGAAAATAGTCTTCA | 51317 |
rs534445593 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | PHF21A | GRCh38.p7 | 11:46065679 | AAATTCAATGGACAC[-/A]AAAGCCTGTCAGTGA | 51317 |
rs534451639 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46008630 | GTGACTCGGTTTTGT[C/G]TATGAAAACCTGGTG | 51317 |
rs534454946 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:45987863 | TGTATCCCACAACCT[A/C]AAGGCAGCACTGCTT | 51317 |
rs534572471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46113154 | ACAGGTCCCAGCATG[C/T]AGTGCTCTAATCTGA | 51317 |
rs534623291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46061780 | TTCTTTGATACTGAA[C/T]TCCCTGTTTTCGGAA | 51317 |
rs534674455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46038100 | CTGTATTGAGTTTAC[C/T]TGTATACTCCTATTT | 51317 |
rs534682051 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46114598 | GGCCAGAGATAGCAG[C/G/T]TGCCATGGTTACTAT | 51317 |
rs534683916 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46044021 | TTGTGGTTAACAGCT[A/G]TAAATTTGTTTTTAC | 51317 |
rs534691483 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46036115 | AGATATCTAAGAAGA[A/C]GACTGGCAGAACATG | 51317 |
rs534710303 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46088125 | GGAGGCAGTTTATAG[C/T]ATCAAAAGAATTATT | 51317 |
rs534712528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45988504 | TATTTTTAACAAAAG[C/T]ACATTCTTAATATCA | 51317 |
rs534719753 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46039893 | CTTATCAATCTGTTT[A/C]GCTTTCTGCATCTTC | 51317 |
rs534729627 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46035387 | TTGCCAGCATCATAC[C/T]GTTCACTGACTAAAC | 51317 |
rs534751504 | in-del | -/TT | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45947568 | AAGATGAATGCTCTC[-/TT]GTTTACCCACAAAAG | 51317 |
rs534783979 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46121891 | TGTGCTGCGGCACCC[A/G]TTGCCTAGGGAAAAA | 51317 |
rs534833882 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46016191 | ATGGGACCACCATCA[C/T]ATATGTGGTCTGTTG | 51317 |
rs534836319 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46052102 | GGGACTCCAGTTCCC[C/T]GGCCACAAAAGGATG | 51317 |
rs534848999 | in-del | -/AAAT | 0.0189856 | 0.0955633 | intron-variant | PHF21A | GRCh38.p7 | 11:46000924 | ACCTCCGTCTCAAAA[-/AAAT]AAATAAATAAATAAA | 51317 |
rs534861257 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46051389 | ATTCTTGTGACAGCC[A/G]GAATGAAAACCAGAG | 51317 |
rs534875286 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46049839 | GCACTGAGAACCATA[A/G]GTTCCTAAAAACAAC | 51317 |
rs534877497 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46005382 | CAGACTGTAGAATAT[C/T]TGCACAATATATTAA | 51317 |
rs534878457 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PHF21A | GRCh38.p7 | 11:45995486 | TTAGATGGTTAAACC[C/T]CTACTCCCGGGTTTA | 51317 |
rs534881989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46042534 | TGGTGAAATGTATAG[C/T]ATGTCTCCTAAACAA | 51317 |
rs534921221 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46122562 | ATGGCATTTACTTTT[C/G]TGCTTTGTGTAGCAG | 51317 |
rs534922362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45952266 | TTGCTTGCCCACACT[A/G]GGTCTAGCTCCATCA | 51317 |
rs534928921 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46111363 | TAATTCCAGCTGCTC[A/C/G]AGAGGCTGAGGCATG | 51317 |
rs534963045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46004459 | GGAAGGGGTAGAGGA[A/G]AGAAGGAAGTCCTTG | 51317 |
rs534964073 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46112423 | TGCCAAGCACCGTGC[C/T]AGGTACGGTCATAGA | 51317 |
rs534995110 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PHF21A | GRCh38.p7 | 11:45974887 | TTGACAAAACCCAAA[C/T]TGCATGAGCTAGAAG | 51317 |
rs535033106 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45976708 | TTAGCTGGGCATGGT[G/T]GCCTGTGCCTGTAGT | 51317 |
rs535040766 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45994196 | AAAATGGAATGGACA[C/T]TGGCAACATTTAGAC | 51317 |
rs535059227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46112314 | TTGTAAAAAGAGAGG[A/G]AAAAAATGTGAAGCG | 51317 |
rs535087267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45943320 | TAGAGACGGGGTTTC[A/G]CTATATTGCCATCAC | 51317 |
rs535103522 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46114146 | CTACAAAGAACACTT[A/T]GAAAAACAGTATTCC | 51317 |
rs535112712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45969181 | CTCAGCCTTCCTACC[A/G]AGGAAGTCAACACTC | 51317 |
rs535121753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46004314 | TGGTCTGACATCACA[A/G]ATGGTGTTTTCTATA | 51317 |
rs535127072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46018703 | CAAAATCCTGATATG[A/G]ACAACACATTTTTTT | 51317 |
rs535128296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45951567 | ACATACACTTTGTGG[C/T]TGCCAACTAACTACA | 51317 |
rs535143798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46060652 | TTCGTGTCCTTTGCC[C/T]ACTTTGTAATGGGAC | 51317 |
rs535149992 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46099405 | GGATGAGCAAAACTA[A/T]CTAAATAAAAATTAT | 51317 |
rs535170768 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45987127 | GGCTCATGCCTGTAG[A/T]CCCAGCTACTTGGGA | 51317 |
rs535175022 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46049124 | CATTGTTGGGGCATT[C/T]TCCTCCTTTTCTCCC | 51317 |
rs535212111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46103499 | TTTTAAAAAACTCGT[C/T]GGAATTTCTCCTCAG | 51317 |
rs535216896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PHF21A | GRCh38.p7 | 11:45934927 | GGAGAAAGCAGGTAA[A/G]CAGGACAGTTCAACT | 51317 |
rs535217035 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45941838 | GGCAATACCAACTGC[A/C]ATTTCATCATGTGCT | 51317 |
rs535226620 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45995257 | TTTTGCCACTAATCA[G/T]AGGGGAGAAAGCACT | 51317 |
rs535241326 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:45960116 | GCTGTGGAAAACAGT[C/T]TGGCAGTTCTTCAAA | 51317 |
rs535241978 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46057107 | ACTACAATTGAGAGG[-/T]TTTTTTCCCCAAGTT | 51317 |
rs535244248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45993374 | TAAGACTCTCAGAAC[C/T]GTGCAGGGCTAATTA | 51317 |
rs535246909 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46104197 | CTTTTATATCTCTGG[A/G]GTTCTACAATTGTTT | 51317 |
rs535252284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45944925 | GAGCACGCCATGCCC[A/G]GCTAATTTTTGTGTT | 51317 |
rs535252538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46050308 | AGGCATAGGGACTAA[C/T]ACCACTGGGTCTTGT | 51317 |
rs535253318 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46101731 | GCCTCGACCTACCAG[G/T]CTTAATCAATCCACC | 51317 |
rs535273883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45941237 | CCAAGTAGCTGGGAC[C/T]ACAAGTGCGTACCAC | 51317 |
rs535274992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46076480 | CCCCATCCCCTATAG[A/G]TAAACTATAGAGTTT | 51317 |
rs535298975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45959218 | GCACCCCACTACACA[C/T]ACAAAAAAGGTTAAC | 51317 |
rs535302180 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46000788 | AGCCAGGTGTGGTGG[C/T]GGGTGCCTGTAATCC | 51317 |
rs535326810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46111567 | ATTGTAAGAACTCCT[C/T]GCAAGAGAAAAAGCT | 51317 |
rs535333965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46094373 | AACCCGGAAAAGTTA[A/G]GTGATTTCCCCAAAG | 51317 |
rs535340634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46069239 | ATTTCCTGTATTTGA[C/T]GAAAACGAGGAGCTG | 51317 |
rs535369007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45984740 | GCTTCTCTCAAAAGA[A/G]ACTCCAAGACCCTGC | 51317 |
rs535373611 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46121270 | GGTTGGGGGGAGGAA[C/T]TGGATCCTCCTCCTC | 51317 |
rs535374477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45950706 | TTTCTCAATGACAGA[A/G]ATCAGTATCTTGTGT | 51317 |
rs535392269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46052267 | AGAGGCAACCTCTGC[C/T]AGTACAGGACAGCCT | 51317 |
rs535479079 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46111116 | AATCACAACTATGTG[C/G/T]GGGGGGAGGCTAGTA | 51317 |
rs535482520 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | PHF21A | GRCh38.p7 | 11:45942229 | GAATGTTTCAATTTT[A/T]AAAAAAACCTGGCAG | 51317 |
rs535484825 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46051468 | AAGAGTTTACTAGGC[C/T]TTCATTTCCAGTGTC | 51317 |
rs535543146 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46086102 | CTATGGTGAACAAAT[C/T]TGGGTAGTTTTAGCT | 51317 |
rs535546789 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46076076 | GATTACCATAAACAT[C/T]TACTTATAGCTCTAT | 51317 |
rs535566316 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46043943 | AAATTATATACTTAA[G/T]GATTTATATCAAGCA | 51317 |
rs535579594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46085286 | TGTCCAGCTTTACAA[C/T]GAAAATCATCTTCTT | 51317 |
rs535625181 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46058937 | AGCAGAAATGAAGCA[C/G]AAGCAAAGAAAGATG | 51317 |
rs535629813 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46018667 | ACATGACTTGGCAAA[A/C]GATAATTTGGTAAAC | 51317 |
rs535718673 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PHF21A | GRCh38.p7 | 11:46059787 | GCTGGAGTGCAGTGG[C/T]TCAATCTCGGCTCAC | 51317 |
rs535730557 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45933643 | CAGAAACAAACCCAT[C/T]GTGGCTGTGGAGGCT | 51317 |
rs535741318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46120033 | GGGGTGAGGGGTGCA[A/G]GCAGACTCTCCGGAA | 51317 |
rs535794801 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46011307 | CAATCTGCCCAACAT[A/G]GTAAAACCCTGTCTC | 51317 |
rs535800061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46002012 | TTCTAGAAGTGGTTC[A/G]GAAGGATTTCATGAG | 51317 |
rs535810137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46101013 | ACAAGAAGGAAGTGC[A/G]GAACAAGACTTGTGA | 51317 |
rs535841710 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46034225 | TTAGTGCCCCCACCC[A/C]CCCCTTGCATACTTT | 51317 |
rs535843117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46039473 | CAGGTAAGTACAGGG[C/T]CCACCTTGAAGGAGG | 51317 |
rs535866216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46030373 | GATCTTTTATTCTTA[C/T]CAAATGATTTGCCCA | 51317 |
rs535905623 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46093136 | AATCAGTGATGAAGC[C/G]AGAAAGAAAATTTAG | 51317 |
rs535907396 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46054518 | TGGTCTAAGGTGCAG[C/G]CCTGTATGCAGGATT | 51317 |
rs535933592 | in-del | -/C | | | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930231 | TGGCTGGAGAGGCAG[-/C]CGTGCATGCGGAGAC | 51317 |
rs535954987 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46025636 | TGACACAATTTCAGG[G/T]TTACAGAAAAGTTGT | 51317 |
rs535972008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46022302 | CTACAAAAAAATTTA[A/G]AAATTAGCCAGGTAT | 51317 |
rs536025138 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45972971 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 51317 |
rs536029043 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45940352 | AGGCGCCCACCACCA[C/T]GCCTGACTAACTTTT | 51317 |
rs536033455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46109711 | ATTGGGCCAGGCGTG[A/G]TGGTTTAGGCCTGTA | 51317 |
rs536064642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46001462 | CCTAGGAAATAAATA[A/G]CAAGACTAACAATAG | 51317 |
rs536075912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45998187 | TTACTCACAGCTAGG[C/T]TTCCATCTGTGTTAT | 51317 |
rs536084167 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PHF21A | GRCh38.p7 | 11:46063188 | TGAATTCGCCGGGGG[A/G]GCTGGCATGTTTATA | 51317 |
rs536099286 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46101685 | TTGCCCAGGCTGGAG[G/T]GCAGTGGCATGGCAC | 51317 |
rs536100060 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46054269 | GATAGTAACCCTTGA[A/C]AATTATATCACATAA | 51317 |
rs536100768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45949074 | CTAATCATCCTAAGG[C/T]CTCAATGCTCAAGGG | 51317 |
rs536137792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45983718 | TCACAATCCAGTCTC[A/G]TTCTAGTTCAGTCTT | 51317 |
rs536151071 | in-del | -/TATT | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46089791 | TATCTTTCTAATCTC[-/TATT]TGTTTTGGAGGGGGT | 51317 |
rs536162690 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46038314 | TGTATTTTTAGTAGA[G/T]ACGGGGTTTCACCAT | 51317 |
rs536162731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46046323 | CAACAAGGCTAATAT[A/G]CAAGGGAAACCCACT | 51317 |
rs536209573 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45972557 | CCGAGGCAGGTGGAT[A/C]GTCTGAGGTCAGGAG | 51317 |
rs536209924 | snp | C/T | 1.6477e-05 | 0.00287024 | intron-variant | PHF21A | GRCh38.p7 | 11:45948843 | AACACACACACAAAG[C/T]AAAAGCAACAGCAGC | 51317 |
rs536213112 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46055994 | TACCTTTTATTGAAA[A/G]TCTTGAAATTTAAAA | 51317 |
rs536251520 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45980942 | GTGGAGTGAAAAATT[A/C]ATGTCAAAGTTCTTC | 51317 |
rs536271179 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46108970 | GTCTTCATTTCCATC[C/T]CATTCCAATGTTTAC | 51317 |
rs536272262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45980577 | TCACAGGTGTAGTCA[C/T]AGTGCATGCACTACA | 51317 |
rs536284187 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:45961867 | TTCTGTCTAAAACGA[A/G]TCTTCAGCTTCAAAG | 51317 |
rs536305649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46006399 | GCACCTAACGAAATA[C/T]TGCAACTTGTTATAG | 51317 |
rs536310819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46114237 | GCTATCAGTAACACG[C/T]CCAAACACAAGCTGA | 51317 |
rs536336950 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46081814 | GAAAAAAGCCATACT[C/T]ATTCATTTATATATT | 51317 |
rs536337607 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46008720 | ATAATAATATATGTT[C/T]TACATATCTCATATA | 51317 |
rs536357861 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:46031006 | AAATAATGCAGAGCC[A/G]TAAGGAGCTAGAGCC | 51317 |
rs536453825 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45957309 | CATAGAAAGAATACT[C/G]CACTCCACAAGAGCA | 51317 |
rs536460644 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46096347 | GTCCCCGTCTAGGCT[C/G]ACGTTTATAGCAAAA | 51317 |
rs536467255 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45977850 | TTCTTCTTCTTTTTT[G/T]TTTTTTGGTATTGAA | 51317 |
rs536471708 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46114912 | GCTTCTGTGTTTAAG[A/T]TATTTTTCCCCTAGG | 51317 |
rs536472641 | snp | C/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | PHF21A, LOC105376661 | GRCh38.p7 | 11:46123375 | TAAAAATTCTGATTT[C/G]TTAAAAAATAAAATA | 51317 |
rs536487770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46063217 | TAAGAGAAGGAGCTC[C/T]TACTATTCTGTATAC | 51317 |
rs536499035 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45945269 | TGAGGTTCATTTAAA[C/G]ATTTAGAGCACTAGT | 51317 |
rs536507899 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930570 | GAAAAAGGACCCACA[A/G]GCAGCAAGAATGCAG | 51317 |
rs536521033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46020534 | TAGCTCCCACTTTCA[C/T]TTTTCTGCTTCCCTT | 51317 |
rs536531008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45979573 | TTTGCTTCTTAGTAA[C/T]GTTATTTCCTTCTGC | 51317 |
rs536538404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45970484 | ACATCAAAATTTAGA[C/T]ATATTTCTCCCAAGC | 51317 |
rs536538529 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46085692 | ATACAATAAGATTCA[C/T]GATCTTCATATTTCT | 51317 |
rs536549306 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46098265 | GGTGTAGTAAACACT[G/T]ATTATCTATTACTTG | 51317 |
rs536556034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46028719 | GCTGGGATTACAGGC[A/G]CCCGCCACCACGCCC | 51317 |
rs536570626 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46088027 | CCTCCCAAAGTGTGG[C/G]ATTACAGGTGTGAGC | 51317 |
rs536571635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45937625 | AGCTGGGATTACAGG[C/T]GCCTGCCACCATGCC | 51317 |
rs536581849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45988765 | CATGGTGGTGGCACA[A/G]TTGTAGTCCCAGCTA | 51317 |
rs536585965 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46106436 | TTTTAGTATCAAGTC[C/G]TGATAAGTTAACGGC | 51317 |
rs536607471 | in-del | -/G | 0.00398564 | 0.0444627 | intron-variant | PHF21A | GRCh38.p7 | 11:46058790 | CTCTTTACAAAATCT[-/G]GAACAAGAACAAGCC | 51317 |
rs536612497 | snp | A/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | PHF21A, LOC105376661 | GRCh38.p7 | 11:46123069 | GTAGCAACTGCCACT[A/T]CGCATTTTCCAGGCA | 51317 |
rs536614949 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45944143 | GGAGCAATCTGAATA[C/T]GGACTGTATATTTTA | 51317 |
rs536616591 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46062064 | GACATCTGATTCCCA[A/G]TCCCTGTTTGCAACT | 51317 |
rs536617376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46071546 | AAATCTTTGACCAGT[C/T]AGGTATAAGTACTGG | 51317 |
rs536651831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46079694 | AAGTTCAGTGGGGCA[A/G]TGATGCTCAGTTTTT | 51317 |
rs536666316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46097363 | GTCCCATCTCCCTAT[C/T]GCTCAATCCTTTCCA | 51317 |
rs536673336 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:46045422 | GAGTTGGGAAAGGTA[A/G]AGAAAGAACAGAGAG | 51317 |
rs536677576 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45985635 | AAAATAATTGCACTT[C/T]CTTCATTTTGTAAGA | 51317 |
rs536685152 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45971551 | TTACTACAGAGAAAG[A/G]CAATCTCTAGTTTTC | 51317 |
rs536691777 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45929276 | CTGGGACTGGAATGT[C/G]TCCTGCCCACCCTCC | 51317 |
rs536706337 | snp | A/G | | | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46085758 | ACCTAAGTTTTCTAA[A/G]AGTCCTTTGAAAACT | 51317 |
rs536708692 | in-del | -/G | 0.175254 | 0.238565 | upstream-variant-2KB | PHF21A, LOC105376661 | GRCh38.p7 | 11:46123021 | TACAAATGGGGGGGT[-/G]GGGGGGTTTTGTTTT | 51317 |
rs536751309 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45953602 | TGTTTGTTTCTCATC[C/T]GTTTCTGTGTGAGAT | 51317 |
rs536780313 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46088898 | GCAGGTCTTTCATTA[A/C]GATTCTAATAACTCG | 51317 |
rs536801793 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46060871 | TTTTGCACCTTCATC[A/G]TGAAATCTGTGCCCA | 51317 |
rs536807203 | snp | C/T | 0.000174932 | 0.0093507 | intron-variant | PHF21A | GRCh38.p7 | 11:45953660 | TAAAAATTCAGAATT[C/T]GTTTTTTATTAAAAG | 51317 |
rs536836589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46037217 | GAAAGGCTATGTTTG[C/T]AGTATATTTTGTGAG | 51317 |
rs536851635 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46027663 | ACATTCTCCTTATTC[A/C]CCTTCCATCACATGA | 51317 |
rs536866831 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46005462 | GGTTTCAAGATAATA[A/C]GAAAAGCAAAAACCT | 51317 |
rs536882356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46044464 | CCCTTTCCACCCCCA[C/T]TTGGATTTCATATCT | 51317 |
rs536901620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46105233 | ACCTCTGTGTTCTAC[C/T]GACACGCTATAAACT | 51317 |
rs536972098 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46054212 | ACTCATTTAAAAAAA[A/T]TTTTTTCTAAAAGGA | 51317 |
rs536982768 | in-del | -/TCTC | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46038115 | TTGTATACTCCTATT[-/TCTC]TCTCTCTCTCTTTTT | 51317 |
rs536989743 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46018979 | ACACACATCATGTAA[G/T]AAGCTAAAACTGTGT | 51317 |
rs537024012 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46019522 | AATTTAGTTAAACAT[A/T]CTCTACCATACCCCT | 51317 |
rs537028199 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46028492 | TTCCCTCCTGAAACT[A/C]TAAGACTTCCTGATT | 51317 |
rs537030393 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46014760 | CCGAGGCGGGCGGAT[C/G]ACGAGGTCAGGAGAT | 51317 |
rs537030500 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45977385 | AAAGTGATCCACCCA[C/T]CTCGGCCTCCCAAAG | 51317 |
rs537101139 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46012726 | CACCCACATTTCTAA[A/T]TCTATCTTAATATCC | 51317 |
rs537107289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46045966 | ACAGAGATAAAGTAC[C/T]GTATTAAAACTCAAT | 51317 |
rs537146579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46029629 | GAAGGCAAAGGTTGC[A/G]GTGAGCCAAGATCGT | 51317 |
rs537152482 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:46038601 | GGAATTTATTTCTTA[C/T]AGGTATGGAGGCTGA | 51317 |
rs537209602 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | PHF21A | GRCh38.p7 | 11:45986595 | GACCTAAAAGTCCAG[-/A]TGGCTTACATTCAAG | 51317 |
rs537211273 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45986919 | AATGACAACTGCCAA[A/C]AAGAAAGTACAATAT | 51317 |
rs537220342 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46033433 | CCACATCTGGCTAAT[C/T]TTTGTATTTTTGGTA | 51317 |
rs537243094 | in-del | -/GGAT | 0.00517822 | 0.0506191 | intron-variant, utr-variant-5-prime | PHF21A | GRCh38.p7 | 11:46118129 | ACTGAATAGGAAAAA[-/GGAT]GGACCCTTCAAAGCT | 51317 |
rs537246471 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45984380 | TTAGATTCCCTTGAC[A/G]TTCGCATCACTGGGT | 51317 |
rs537247166 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45995084 | GCTTAGATGTTGAGA[A/C]TGAGAAGAGACAATT | 51317 |
rs537256096 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45948240 | TGGTGAGAGACACTG[A/C]TGCTGCTACTGCTAT | 51317 |
rs537257538 | in-del | -/TTTC | | | intron-variant | PHF21A | GRCh38.p7 | 11:46022142 | ACCATGTACTGTTTG[-/TTTC]TTTCTTTTTTTATTT | 51317 |
rs537264587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46103189 | AACTCAACCCCCAAA[C/T]GCTTGTAGAATCTCT | 51317 |
rs537312682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46027529 | ATGCCTGCACAGGAA[A/G]CACACAAAATACAAT | 51317 |
rs537343768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45977767 | TAGCTATCTGATTTA[C/T]AACAGGGATTTTTCT | 51317 |
rs537345815 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46036154 | ATTTCGGAGATGAGT[A/G]AAAGGGAAGAATCAA | 51317 |
rs537365406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46044721 | TAAAATTCCTTTTAA[A/G]GAAAAAAAAATCTGC | 51317 |
rs537370971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45996590 | CAGGAATGCTACTCT[C/T]CATATGCACAAAGGT | 51317 |
rs537385324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46114126 | ATCCCCACACACACA[C/T]GCTTCTACAAAGAAC | 51317 |
rs537388657 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46040441 | ATTATAAGTAGAAGA[C/G]AAAATGTCTGAATAG | 51317 |
rs537392326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46104553 | ACTCATTAGATAACA[C/T]TTTTATCATCTATAC | 51317 |
rs537394968 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45980306 | GCAGGACTCTGGAGC[C/T]ATCCTACTTCAACTC | 51317 |
rs537396146 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46057529 | AAAAACTGTACTTTC[C/T]GTTCTCCATGTTTTG | 51317 |
rs537408316 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46065918 | GGAGCTACTGGCTCA[C/G]AGAAGAGAAACCACC | 51317 |
rs537412380 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45998659 | CTGGGATTACAGGTA[C/T]GCGCCACCATGCCCA | 51317 |
rs537414951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46079051 | AAAAGTTAAGTACCA[C/T]CTATATTTAAGTATT | 51317 |
rs537417935 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45962106 | CCTCAGTGCCTGCTC[C/G]AAACACACTAGAAAC | 51317 |
rs537419397 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | PHF21A | GRCh38.p7 | 11:46003215 | TATGAGAGTGCCACT[-/A]AAAAAAGTCCTAAAA | 51317 |
rs537426066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46024450 | AAGCTTCTCTCTGAT[A/G]TGGCCACCTAGTTTA | 51317 |
rs537452221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45996171 | CTGGTCAGAAACCCC[C/T]GGCTTCAAGTCACCC | 51317 |
rs537457752 | in-del | -/CTT | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46024320 | TCTCTTTCCTCTGTC[-/CTT]CTCTTTTTCTTGTAG | 51317 |
rs537491640 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | PHF21A | GRCh38.p7 | 11:46096314 | ACCCTCTTGACTCCA[A/T]ATCCTTCTCTAGTTA | 51317 |
rs537526074 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46122651 | AAGTATTTTATGCCT[A/G]TTCTACCTCCAAGGA | 51317 |
rs537532191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45961791 | TTAGAGCGCTGGAGA[A/G]GACAAGGACAGGGGA | 51317 |
rs537561922 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45951668 | GATGAAGCAGTGTGT[A/G]GACTGATATTCAGAT | 51317 |
rs537585290 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46008957 | GTGAACTCAACAAAT[C/T]GGTTCACATTTCACT | 51317 |
rs537590550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46016853 | CTTAAAAATTAAACA[A/G]ACACGACCTCAACCA | 51317 |
rs537595823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46011895 | CTTCTTTAGTGTAAC[A/G]TTAATTTTAAAACAT | 51317 |
rs537601836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45973379 | TCTACTTAGGGGTAT[C/T]AAGTTGTTTGCTTCT | 51317 |
rs537608817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45982863 | TAAACATGACACCTG[C/T]CAAAAAATAAACTTT | 51317 |
rs537612570 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45977011 | TCAGGTGGGCTACTG[C/G]ATGGAGAGGTGCTAT | 51317 |
rs537642530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46031221 | CAATAATGTCCCTTC[C/T]AACCTCTTTCCATAC | 51317 |
rs537670813 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | PHF21A | GRCh38.p7 | 11:45982172 | ATGTTGCCCAGGCTG[A/G]TCTCAAACTCCTGAG | 51317 |
rs537678035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46052131 | TGACTGATTCAAGAA[C/T]GGACCTAAAACTTGT | 51317 |
rs537681334 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46040112 | CTGTGCCAGATATAA[C/G]AGGGTTACTAGATGT | 51317 |
rs537712171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46023888 | TTGAACCCAGGAGGC[A/G]GAGGTTGCAGTGAGC | 51317 |
rs537804396 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46016556 | ATTTCTTACATAAAC[C/G]CTTCCCTAATCCCCT | 51317 |
rs537815815 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45956905 | CATGATCTAATGATA[C/T]GCTGTAAGAGAGACT | 51317 |
rs537818658 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46060635 | CTTTTGAAAAGTGTC[C/T]GTTCGTGTCCTTTGC | 51317 |
rs537826082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46116055 | AAATTTAAGATACTA[C/T]ACCTTTTGATAGGCT | 51317 |
rs537841338 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46074122 | GGTTTTGTCAGATGC[A/C]AAAAAAAAAAAAGTT | 51317 |
rs537895576 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45955599 | AATCAATTCCTTTCC[A/C]CTAAAAAATTACCCA | 51317 |
rs537898162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45946309 | GAAGTTCCTGGACTA[C/T]TGCAATTTGAGATTT | 51317 |
rs537903382 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46108192 | ACCAGTTTTTTTAAA[G/T]GTTATTTGAAAACAC | 51317 |
rs537921526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46066959 | CGTATGTCTGTTTTA[C/T]AATTTGCTTTTTTAA | 51317 |
rs537940206 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45990823 | CCACCCCACATCTCC[A/C]CACTATCAACAAGCT | 51317 |
rs537947352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45948448 | TTTCCTTCCTGGAAA[A/G]TCTGCAGCTCCAAGA | 51317 |
rs537951468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45958015 | AACAAACTAGACAAC[A/G]TAGATGCAATGGAAA | 51317 |
rs538018648 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45931776 | CCACCGCCCTCCCAT[C/T]GGCCAGGGGCACGCA | 51317 |
rs538020051 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46072491 | GGGTTCCCTGACATC[A/G]TGGAACCACTCTCAG | 51317 |
rs538021329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45963549 | GATTACGGGGAAAAG[C/T]ACCTTCTACAATTTA | 51317 |
rs538033761 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46040665 | TGGTAACAAACCCTT[A/G]CTCACAATTCTATCC | 51317 |
rs538034289 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46026704 | TGTGGGCTTTTAAAT[A/C]CGTAATTAAAAAACC | 51317 |
rs538051706 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46080725 | CAGGCTGGAGTGCAG[C/T]GGCACAATCATAGCT | 51317 |
rs538061157 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PHF21A | GRCh38.p7 | 11:46100111 | GGAGTCTGAAACATG[C/G]CTCAATCACGCTGAT | 51317 |
rs538144826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46031975 | ACATCTTTTTGTTCT[C/T]TTCCACACTAACATG | 51317 |
rs538160468 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45954608 | CTTCAAACACAAAAG[A/G]TAGCTAGCATACTGG | 51317 |
rs538170060 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46091424 | AGCCATTAAAAAAAC[A/C]TCTCAAAGTAGATAT | 51317 |
rs538184225 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46067380 | TCTGAGGTAAGTGAC[A/G]TAGTAACATTGCAGA | 51317 |
rs538193220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46055886 | AATTGAATAGTTTTG[C/T]TTTGCTAATTCAGAA | 51317 |
rs538226483 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46031802 | AACACTATACGCAAA[A/G]GCTGGAAGAATCTGT | 51317 |
rs538230770 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45991693 | GTCACTAAACAAGGT[C/T]TGTGACCTTTGGTCA | 51317 |
rs538230839 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46029107 | TATCTGTCATGATAA[C/G]CTAAACCTTGTGGAA | 51317 |
rs538256102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46007720 | TTAGTTACATTAATT[C/T]AAATCAAAAAACGAT | 51317 |
rs538266094 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46081918 | CAGAAATATTTTACT[C/G]TGTGTCCCTTTACAA | 51317 |
rs538299756 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45931117 | AGCCCAGCTGCAGGC[A/G]AGGTCAGAATGTACC | 51317 |
rs538334286 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45959563 | CAATTAGGCAAGAAA[A/G]AGAAAAGGCACCCAA | 51317 |
rs538343644 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45955830 | AGGTGTGAGGAACGG[A/G]ACCTCCAGCCAACAG | 51317 |
rs538358206 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45938526 | ACAATAGTCCCCCCT[A/T]ATCCTTGGGGAATAT | 51317 |
rs538366963 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46047741 | GTTGTGTAAGCTTAA[A/G]AGAAGTCACTTTTTC | 51317 |
rs538370966 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45956770 | ATGAAGAACAAAAAA[C/T]GTAAGATATACAGAA | 51317 |
rs538388140 | snp | A/G | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46023736 | AGAGGTGGGCGGATC[A/G]CCTGAGGTCAGGAGT | 51317 |
rs538394578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46015049 | TAGTTATTCTGACTG[A/G]TGTAAAGTGGTATCA | 51317 |
rs538446369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46038800 | ATGATAACCCATGAA[C/T]CTGTGGATTGATTAA | 51317 |
rs538463071 | in-del | -/TAAG | | | intron-variant | PHF21A | GRCh38.p7 | 11:46100574 | TATTAAAGGTCCTGT[-/TAAG]TAAGTATACTCCTTG | 51317 |
rs538480563 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45989675 | CTGTCTCAAAATAAA[A/T]AAATAAATAAATAAA | 51317 |
rs538486481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46046483 | AGAGCTCGTCATACA[A/G]GGCAAGAGAAAAGCC | 51317 |
rs538497148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46014788 | GATCGAGACCATCCC[A/G]GCTAAAACGGTGAAA | 51317 |
rs538499269 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46097148 | CAACAGCCTCCTAAC[G/T]GGCCTCCCCAATTCT | 51317 |
rs538516566 | in-del | -/AT | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46109679 | CACACACGTAAACAC[-/AT]GTCAAGAATTTGTCT | 51317 |
rs538557744 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46038891 | TGCTGCCACATTGGG[G/T]ATTAAGTTTCCAACG | 51317 |
rs538588075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45965003 | GCGTTTTCTGTTTAC[C/T]ACCTCATCTGTGCTT | 51317 |
rs538594889 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45980655 | GTAGCTGGAACTACA[A/G]GCACACACCACTGGG | 51317 |
rs538601190 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:45960191 | GGTATATACCCTAAA[A/G]AACTGAAAACAAGTA | 51317 |
rs538633735 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PHF21A | GRCh38.p7 | 11:46006697 | CAGCTGGTCAAATGT[C/T]TTATTTAAAAAGATA | 51317 |
rs538645269 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46091296 | ATTCCAGCTATCTTA[G/T]TTGAGTGTAATTTTT | 51317 |
rs538676450 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45963415 | ACAAGAGTAAAACTC[G/T]GTGTCAAAAAAAAAA | 51317 |
rs538709033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45998806 | ATTACAGGCATGAGC[C/T]ACCACACCCGGCCTT | 51317 |
rs538714588 | snp | C/T | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46073958 | ACTGAGTTTTAGTCA[C/T]GAAGGATGCTCACTA | 51317 |
rs538725735 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45965951 | CCAATAGCCTTAACT[C/T]GCATTTGAAATTTCT | 51317 |
rs538799373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45971702 | ATACTTAATTCTTTT[A/G]GTTTTTCTAGTTCTT | 51317 |
rs538800882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46115103 | TGAGATATTTTCACC[A/G]AAGTCTTTTTTATTT | 51317 |
rs538811363 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45938391 | CACATTCTAGATGCA[A/T]ATAAATGTTTTAGGA | 51317 |
rs538833347 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45961728 | GCATAATCTAATAAA[C/T]ATTAAATACCTGACT | 51317 |
rs538847181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46107409 | ATACTCTGTAGGACA[C/T]GGTCTGAGCCACTCA | 51317 |
rs538858080 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46098446 | TCTAAGTCTTCTTAC[A/G]ATATAAACAAAAACT | 51317 |
rs538928138 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46039747 | CAAACTAAAATTACA[C/G]ATCACTATCAGGATC | 51317 |
rs538929676 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:46090509 | AGAATGCTGCATATC[A/C]TATCCCCCTCTTGGA | 51317 |
rs538936631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46013634 | CCTTAGGTCATTTCA[C/T]TGCTGTGCGAACATC | 51317 |
rs538946850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46071647 | CATCCAGTCATCACA[C/T]ATCTAGGAATTTCTC | 51317 |
rs538949684 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45931047 | GGTTGCATCTCGTAC[C/T]CCATACTAGCTGACT | 51317 |
rs538960701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45990658 | CAGCAAAAGTATTGA[C/T]ATGCATGGTCAAAAG | 51317 |
rs538996868 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45945329 | CTACTAAGTATTTGA[C/T]AGTTTTTCCGGAACC | 51317 |
rs539004392 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46021408 | ATTTTAAACTATTAA[A/C]AAGTATACACCATAC | 51317 |
rs539008010 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:46014181 | CCCTACTCACTTGTG[C/G]AGTCCCTAGTGTTTA | 51317 |
rs539017408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46119899 | CCCGGCGGGGGCGCG[A/G]GCGGGGGAGGGGCGG | 51317 |
rs539030861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45950371 | GGCGGGTCTCATGAA[C/T]GCACAAGAGCAGGCA | 51317 |
rs539060259 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46002385 | TCAGAAATAAACTAA[A/T]TTGTAACTTTACTAC | 51317 |
rs539068934 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46072320 | CATGGGATCTAACTG[G/T]AAGTGGTGCATGCAA | 51317 |
rs539080993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46062646 | TTAAATATCTAGTGA[C/T]TCTTGGCTATGTTCA | 51317 |
rs539081256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46115912 | TGTCTGTAGGATGAA[A/G]AAGTTAATAACACCC | 51317 |
rs539101029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46112081 | CAAAGGCTTGTGGTA[C/T]GGATGCAATGAGTAC | 51317 |
rs539190715 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46001624 | CTACATTCTTTTCCC[C/G]CATGCTTACATTTTT | 51317 |
rs539199895 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45967362 | GATAGAGTGAGACCC[A/T]GTCTTAAAAAAAAAA | 51317 |
rs539205136 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:45980625 | TCAAGCAATCTTCTC[A/G]CTTCAGCATCCCAAG | 51317 |
rs539214590 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46097010 | TTTTACCACACTCCA[C/T]ATCTACTCCGACAGC | 51317 |
rs539215243 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46029556 | AGCTGGGCGTGGTAG[C/T]GCATGTCTGTAATCC | 51317 |
rs539236379 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45979170 | TACAGGCGCCTGCTA[A/C]CAGGCCTGGCTAATT | 51317 |
rs539239146 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46080297 | CCGAGTGGCTAGGAC[C/T]CCAGGTGCACACCAG | 51317 |
rs539263415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45966804 | TTGTATTTTTAGTAC[A/G]GACAGGGTTTCACCA | 51317 |
rs539269199 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | PHF21A | GRCh38.p7 | 11:46007199 | CATGCAAAGTGATAG[C/T]GAGGTTCTAAGAGAT | 51317 |
rs539291796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46022123 | TTTTCTATTATAGAA[C/T]AAAACCATGTACTGT | 51317 |
rs539302016 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46080642 | ACGTCAAGTAGTCAG[C/T]CAGCACATTTTGCTA | 51317 |
rs539302269 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45952373 | CAGCCTCCTGGGTAG[C/T]TGGGACTACAGACAT | 51317 |
rs539331350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46119250 | GACTATTAGCAAAAA[C/T]GCACAACTCCTTCCC | 51317 |
rs539337654 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46076453 | ATCACCTATTCTCAC[C/T]AACTGCCTTTACCCC | 51317 |
rs539381647 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46005514 | TAATGGGCACCAAAT[G/T]TTCAGACCTTCCTGT | 51317 |
rs539399398 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46059677 | TCCTTCTGCCTCAGC[A/C]TCCCAAAGTGCTAGG | 51317 |
rs539426359 | snp | C/G | | | intron-variant, downstream-variant-500B | PHF21A | GRCh38.p7 | 11:45935047 | TGGCTCCTTGCCTGG[C/G]AGAAGCCTCTGTCCC | 51317 |
rs539448723 | snp | A/G | 3.29625e-05 | 0.00405958 | intron-variant | PHF21A | GRCh38.p7 | 11:45949516 | TTCATTAGCAGAGAG[A/G]CATGGAGAACCTAAA | 51317 |
rs539475911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46102389 | AAAGGAAAGGGTCTG[C/T]TACTTTGCAACTATC | 51317 |
rs539489714 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46059165 | AATAATCAAAATTAC[A/G]TACAAATATTTACGT | 51317 |
rs539491195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45940264 | GCAGTGGCGCGATCT[C/T]GGCTCACTGCAACCT | 51317 |
rs539522082 | in-del | -/AAC | 0.414489 | 0.188264 | intron-variant | PHF21A | GRCh38.p7 | 11:46088411 | TAACTTTCCAATAAC[-/AAC]AACAACAACAACAAC | 51317 |
rs539523687 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45984552 | CCTGAAGAAAAATAC[A/G]GAATTTTATAGGTCT | 51317 |
rs539541450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46092921 | CCACCATGCCTGGCT[A/G]TTACTTTATTTTTTT | 51317 |
rs539543268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46084458 | AAACAATTCTTCAAG[C/T]ATTCCTCTAAAGAAC | 51317 |
rs539552805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46042420 | TCACCACTTGAGCTG[A/G]TCTACGCTGAGGTAC | 51317 |
rs539563854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46051420 | CATTTACCATTACCT[C/T]CCACCTCCATTCTCA | 51317 |
rs539564378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45968866 | AACCTGGTGGGTGGA[A/G]ATTGCAGTGAGCCTA | 51317 |
rs539569929 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46074487 | GCATATAGCATTAGG[A/T]AACTGTTCTAAAATA | 51317 |
rs539578986 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:46092066 | GTGCAAATAGCAAAG[A/C]CCCATTTCTGAGAGA | 51317 |
rs539580712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46101585 | ATGTTTTTCTCTAAG[C/T]ATAATTAAATAATAG | 51317 |
rs539592180 | snp | G/T | | | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46084902 | AGCCAGGATGGTCTT[G/T]ATCTCCTGACCTCGT | 51317 |
rs539592635 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46075889 | CATAAAAATCAGTTA[G/T]TGAGAACTATTTAGT | 51317 |
rs539594106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46024769 | TGTGCCACTGCACTC[C/T]AGCCTGGGTGACCAA | 51317 |
rs539600629 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46041122 | TTTTTTAAACATGTA[C/T]AAAAATCCACCTTCT | 51317 |
rs539603389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46057021 | AGATGGTTATAGTAA[A/G]TGCCGAAAAAATTAA | 51317 |
rs539638983 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46076509 | TTAATTAACACAGTT[A/G]ACGGCAGCCTGCCAC | 51317 |
rs539670752 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46010534 | CATTGTTTGGGAATA[C/G]TGGTATGAATAACTC | 51317 |
rs539748930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45939468 | AATTAAATTCATATG[C/T]GAGTTCTTTCTAAAA | 51317 |
rs539758745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46048776 | CTCCATCTCAAAAAA[A/G]AAATAATTTTTTTTT | 51317 |
rs539763720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46017921 | AATTTATTATTTTGG[C/T]TAAATTCATTACTCT | 51317 |
rs539767198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46057741 | CTATGAAACTGAGAT[C/T]GGGTCTCATGAGAAG | 51317 |
rs539770935 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46009498 | CATGTAACGATAATA[G/T]CAGCTGCACACATTT | 51317 |
rs539782702 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46028312 | TCTCATATTAATTTC[C/T]ATAAAAATAATAATA | 51317 |
rs539786339 | in-del | -/A | 0.00636936 | 0.0560724 | intron-variant | PHF21A | GRCh38.p7 | 11:46026635 | TGAATTAGAAAATGC[-/A]AAAAAAAAATCCTTT | 51317 |
rs539788194 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46108662 | TTTTCTACTTTATAC[A/G]TATCTATATTGCTAG | 51317 |
rs539812948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46041676 | AAAACAAAGAAAACA[C/T]TTATTTTTAAGACTT | 51317 |
rs539841300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46100876 | AGCAAGTTTCTAACC[A/G]CTGTTACCACGTCTA | 51317 |
rs539851442 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46104945 | GCTCAGGCTCTTATA[C/T]TAATACTTGTCTCAA | 51317 |
rs539866643 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45992433 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 51317 |
rs539898000 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45975079 | AGCACTTTGGGAGGC[G/T]AAGGTGGGCGGATCA | 51317 |
rs539958722 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46041188 | TCAAATACAGAAGCG[A/G]AAATAGTCACCTTTT | 51317 |
rs539986476 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46001570 | CACTGCTAGCTAACA[A/C]TGAATTTTTGTATAA | 51317 |
rs540000253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46109937 | AGTGAGCTGAGATGG[C/T]CCCCCTGCACTCCAG | 51317 |
rs540006560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45966145 | GTTCTCATTATTCCT[A/G]GGAGCTTTTGCCCAT | 51317 |
rs540007981 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46117149 | TGAAGAACTTTTATA[C/T]GTATTATCTCATTTG | 51317 |
rs540027269 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46109426 | AAACATTTAAAATCT[A/G]TGTCATTTCTCCAAA | 51317 |
rs540035651 | in-del | -/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46034221 | ATATTAGTGCCCCCA[-/C]CCCCCCCCTTGCATA | 51317 |
rs540037667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46008769 | TTTTGTTAGATTTAA[A/G]TAAATAAATGTAAAT | 51317 |
rs540043225 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46106122 | TTGCCACATTTTCTG[C/G]GCTCTCTTTTGAATT | 51317 |
rs540048419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46023911 | CAGTGAGCCAAGATC[A/G]TGCCATTGCACTCCA | 51317 |
rs540064692 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46083569 | CCAAGGATTAGATAC[A/G]TGCATGTGTATGTGT | 51317 |
rs540065645 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46070198 | CTTCTTTCCCAAAAG[C/T]TTCAGAATCTTGTAT | 51317 |
rs540070807 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46031743 | CTGTTAGGTCTAATA[C/G]TGTCTGGAAAAGAAT | 51317 |
rs540111486 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46009069 | AACCTCCACCCCCTG[C/G]GTTCAAGCGATTCTC | 51317 |
rs540122941 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46105501 | ACCAGGAACTGCAAG[A/G]AATGGGCAATTCAGA | 51317 |
rs540125720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45991580 | CACACACATGCACGC[A/G]TGCACTTTTTCTCCT | 51317 |
rs540131121 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:45999738 | ACTTATTTAGTGATG[A/G]CAAAGCACAGAGATG | 51317 |
rs540139370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46056410 | GAGGTGATGACAAAA[A/G]GAAAACTTTTACTTT | 51317 |
rs540144155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46117688 | AAGCCCTAAATCATA[C/T]CAACTACTTTTGTTT | 51317 |
rs540147551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45957032 | ACTGTTACGAGAGAC[A/G]AAGAACCTCATTATA | 51317 |
rs540162677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46000208 | CGAAGAAACTGCTAC[A/G]CTATTTCCCTCACTA | 51317 |
rs540181107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46049192 | ACAGCTTTTTACACA[C/T]AAACTAATGTTGTTC | 51317 |
rs540200435 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45939825 | GTCTTTTCCAGAGAG[G/T]CAATGCCTAGCTCAT | 51317 |
rs540201131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46116689 | AAAATTTAGGCCGGG[C/T]GTGGTGGCTCACGCC | 51317 |
rs540208628 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46108922 | CTTGGCAATGGATAT[A/C]CAAGGATAAACAAAG | 51317 |
rs540217858 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46020753 | GTCCTATAAAGCCAT[A/G]ATAGTTATGGTTGAA | 51317 |
rs540221345 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46030627 | CAAAAAGATTCTTTA[A/C]TCCTAAAACACATAT | 51317 |
rs540236576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45981181 | ACTTGAGGTCAGGAG[C/T]TCAAGACCAGCCTGG | 51317 |
rs540249848 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45931188 | CTAGCCCCGTCCTCC[A/G]ACCCAAGACTCCTAA | 51317 |
rs540256031 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46099468 | CTCAATATAGCACTG[C/T]TGTACTCACTAGGCT | 51317 |
rs540258714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45948562 | TCTGCTTAATGACTC[C/T]CAAATGCTTCCTTTT | 51317 |
rs540260739 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46084429 | AATTTCCCAAAGAGA[-/T]TTTTTTTCCCTCAAA | 51317 |
rs540267166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46057295 | ATAAGTTTTATGGGA[A/G]AGAGTTTCCCATCAG | 51317 |
rs540278493 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46043433 | TTCTGGTTAACATAC[A/T]ACCTTCTATATCTAG | 51317 |
rs540287044 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:46091778 | AAGCTGGATGACTTG[A/T]ATTGGCTCAAGCCAT | 51317 |
rs540292689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46089892 | GGCTATTATGGTGCC[C/T]TGGGCCAGGCCAGGG | 51317 |
rs540295099 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45983352 | ATTACAGGTCAGATC[A/G]TATGAGCTGGGTAAA | 51317 |
rs540297330 | in-del | -/GC | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46094871 | CGCCACTACACTCCA[-/GC]CTGGCGACAGAGTGA | 51317 |
rs540312951 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46047806 | TGGGGATCAAATTAC[A/G]TAAAGCATGTGAAAA | 51317 |
rs540323992 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45932301 | GGATCTTATTTAGGC[A/G]CCAGCCTTTTGCTCT | 51317 |
rs540332004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45940431 | GAACTCCTGACCTCA[C/T]GATCTGCCCACCTCG | 51317 |
rs540350430 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45964460 | CTGAACAGCCTCTCT[C/G]AATCATGGTCCATCC | 51317 |
rs540368399 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:45972890 | CTGCACTCAGCCTGG[G/T]GAGAGAGCGAGTCTC | 51317 |
rs540377535 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45956069 | AGAATTCTATATCCT[G/T]CAAAACTATTCTTCA | 51317 |
rs540392949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46022579 | CAATCCTCCAGCCTC[A/G]GTCTCCCAAGCAGCT | 51317 |
rs540404215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46081372 | ATTTTTACATTAATG[C/T]TAGCCACAGTCTTCA | 51317 |
rs540431657 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46063752 | TTAAAGAGTTATATA[A/T]AATTTTATCAGCTAT | 51317 |
rs540434594 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46073451 | AGAGCTTGATGTTAA[A/C]AAAATTTTTTAAATC | 51317 |
rs540437150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45937112 | CTGAGAGAAGTGTTC[C/T]GCTGCACCACAGGCT | 51317 |
rs540453192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46023241 | TAAGCAATGGTTTCT[C/T]AGCCTTCCATAAGGC | 51317 |
rs540454327 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45945573 | ACCCCATCTGTTTTC[G/T]GAGAACTCATTCACA | 51317 |
rs540454431 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PHF21A | GRCh38.p7 | 11:45954801 | TTTCATATGGCAACA[A/G]TAATTAAATAAGTGA | 51317 |
rs540455695 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45998589 | GTGATCTTGGCTCGG[C/T]GCAACCTCCACCTCC | 51317 |
rs540487013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46098651 | CTTAGTAAATCACTC[C/T]TTATCCCAAGACAAC | 51317 |
rs540515208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46066220 | GGAGGTAGTGAACTG[A/G]GGAAGGACGAAGGGA | 51317 |
rs540521604 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45947325 | CAAAGGAAAAAAAAG[C/G]GCCAGAGAGATACAA | 51317 |
rs540530960 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45989346 | TTAATGAATAAAACA[A/G]ATTTGGTTAAAAATT | 51317 |
rs540572865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46106741 | ACCAAGCTATCCTGC[A/G]TTCTATAAACTGCCT | 51317 |
rs540589037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46040242 | GAGTTTCATTAAACA[C/T]AATGGTCTCACCTCA | 51317 |
rs540618379 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45989106 | AGCCTGCCAAAATAA[A/T]TACTGATTAACTTCA | 51317 |
rs540621033 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46062965 | GAAGGATGAGCGAGA[C/T]GACCAAGAACACTTC | 51317 |
rs540626560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45977348 | TGCCATGTTGGCCAG[A/G]CTGGTCTCAAACTCC | 51317 |
rs540670897 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930867 | GGAGGTGGCTGGGGT[A/G]GGGCAGTGTCACGAG | 51317 |
rs540675703 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46039050 | ATTACTGGAGCAGAG[C/T]GAGTGGGCTGAATAA | 51317 |
rs540687225 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46094878 | ACACTCCAGCCTGGC[A/G]ACAGAGTGAGTCTCC | 51317 |
rs540702875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45969680 | CTTCATAGTACAGAA[A/G]TCAACAGTCAGAATG | 51317 |
rs540735782 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46019723 | CTCCGGTTAGATTTA[A/T]CTGGTTCCTTTGTTT | 51317 |
rs540751043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46031463 | GGAAGGGAAGGTAAT[A/G]GGAGCTGGAGCCTGG | 51317 |
rs540764740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45968708 | CCGAGGCAGGTGGAT[C/T]ACCCTGAGGTCAGGA | 51317 |
rs540766692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45977942 | CTTAGCTACACCACA[C/T]ACCACCCTCCATGAT | 51317 |
rs540772500 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46111487 | TCTCAAATAAATAAA[A/T]AAATAAATAAATAAA | 51317 |
rs540790079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46055312 | GGTTTTTTAAAACTC[A/G]TTGGTTTAATAATAG | 51317 |
rs540806451 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46115455 | CAAACATACAAAGTA[C/G]AAAACATAAGCTATT | 51317 |
rs540809695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46101961 | CTCCTGTGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 51317 |
rs540847253 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45992643 | ATCAAAATTTTATCA[C/T]AATGGAAGAGCTGGG | 51317 |
rs540852784 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | PHF21A | GRCh38.p7 | 11:45941668 | CCTAAAAAGAGCAGA[C/G]GAAGTCCTACGGAGG | 51317 |
rs540873239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46059816 | ACTGCAACTTCTGCC[C/T]CCCAGATTCAAGCAA | 51317 |
rs540880218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45990089 | AATTACAAAATCTAA[C/T]TACAAAATCTAATCC | 51317 |
rs540888638 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:45978779 | TCATTTCCAAATACG[C/T]CCTTTTTGTGTATCT | 51317 |
rs540910271 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46047024 | AATTTAAAGTGATTC[A/T]GGAAGTCTATTCAAA | 51317 |
rs540930082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45934436 | GGCTGGGGGGTCCCA[A/G]GTCCCAGAGGCAACA | 51317 |
rs540931449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45938011 | AAGGCCATGCGCCTG[C/T]GTGCTGTGTCATAAA | 51317 |
rs540967882 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45998962 | CTCCCGAATAGCTGG[G/T]ATTACAGGCACCTGC | 51317 |
rs540971251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46102960 | ATAACAGGCAGGGGA[C/T]GGAAAGAGACCATCA | 51317 |
rs540972560 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45994633 | GCCTCACCAAGAGTG[A/G]TTATGTTTTAGGCTT | 51317 |
rs540997645 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46068276 | TCAATAAATATATGT[A/G]GAATAAAACAGATGA | 51317 |
rs541017417 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45994682 | GGGGTTTTGCTGTTG[C/T]ATCATTCTGCAACAC | 51317 |
rs541020867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46036300 | TGAGTACAGTTCAGG[A/G]CATCCTGAGTCTAAG | 51317 |
rs541021949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45959541 | GTACTGGAAGTTTAG[A/G]CCAGAGCAATTAGGC | 51317 |
rs541024631 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46047460 | AAATATTCCTGGCTT[C/G]TTCTTCTGGATAAAG | 51317 |
rs541043906 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45987352 | ATCTGCACAATTTAG[C/G]TGTTTGTTACCATAA | 51317 |
rs541055643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46035886 | AGCCACGTTAAGATT[C/T]TGGACTTGGTCCTAA | 51317 |
rs541059768 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46042157 | TTTTTAGGGTGCCAG[G/T]CAACTTAATATAATA | 51317 |
rs541073001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46076165 | CATACAAAAAATTCC[A/G]AAGAATATTTTCCAG | 51317 |
rs541085825 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46037469 | CAACATGGAGAAACC[C/T]CGTCTCTACTAAAAA | 51317 |
rs541110134 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46059206 | ACACTGCAGAGCTAG[A/G]CATACAACAGTAAAA | 51317 |
rs541146453 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46120078 | AGAAGAAGAATAAGC[A/G]GAATTTCCCCAACGC | 51317 |
rs541154505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45949690 | CCACGCTGTCCTACA[C/T]GTGGTTCTCTGTTGA | 51317 |
rs541207010 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45993883 | GTTACACCGACAGTG[A/C]CTATCTGAGATGAAT | 51317 |
rs541212761 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:46003356 | CTCAGACTCTCTTCG[C/G]TGTTAATACTGTTAC | 51317 |
rs541246968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45950834 | CAAGCTCCAAATCCT[A/G]AGTGTTTCACTTGTC | 51317 |
rs541259082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46041833 | TCTGAAAGTACGCCA[A/G]ATGACATTATTACAT | 51317 |
rs541266752 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45959354 | TATTTTAAAAATTCC[A/T]GTTATCTATTCATAA | 51317 |
rs541266934 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46050780 | GGAACACATCAGCCT[A/G]TGTGGCTCTTGGCAT | 51317 |
rs541277197 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45975959 | CCATTCGTCCTTGCC[C/T]TCATACATTAAATAT | 51317 |
rs541346341 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46034289 | CATAAGAACTCTTTA[C/T]ATGTAAGACTAATAA | 51317 |
rs541360576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46085440 | TAATTTAAATTATTT[C/T]GATGGCTAATTTATC | 51317 |
rs541423266 | in-del | -/CTTTAGAC | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45986211 | CTCTAAAAATTTAGA[-/CTTTAGAC]CTTTTATTTGCTAGC | 51317 |
rs541424449 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45933794 | ACACACAGAATAAGA[A/G]GGATCAATTGGCAAA | 51317 |
rs541424636 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46094491 | TTCTCTTAACCCGCT[A/G]CAGGAGTTACTCTTC | 51317 |
rs541439732 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45966713 | CAGCCTCCGCCTCCC[A/G]GGTTCAAGTGATTCT | 51317 |
rs541504699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45977187 | CTCTGTCGCCCAGCA[C/T]GGAGTGCAGTACGAT | 51317 |
rs541507931 | snp | A/G | 5.42706e-05 | 0.00520888 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45933936 | GTTCTCCTTGCCGCC[A/G]GGATCCCGTGGCTTC | 51317 |
rs541512032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46011381 | GTAATCCCAGGTACT[C/T]AGGAGGCTGAGGCAG | 51317 |
rs541547146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46010638 | TCAACAATCACAAAA[C/T]AAAACAATCTTGGCT | 51317 |
rs541557747 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46119473 | ACAAAGAATATTTCA[A/T]CATATGACCGGAATA | 51317 |
rs541595675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46094537 | AATAAACACTAGCGA[A/G]ATATTTTTGGAAAAG | 51317 |
rs541610956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46110234 | GGCCCTTATTATTAT[C/T]CCCATTTTACCACTG | 51317 |
rs541655080 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45939472 | AAATTCATATGCGAG[C/T]TCTTTCTAAAATGAA | 51317 |
rs541658100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45949255 | TGACTAATAAAAATG[A/G]TAAGTCAAAAAAAAT | 51317 |
rs541664927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46092238 | CCTATAACAGAAGAA[C/T]GGGAAAATGGAATTA | 51317 |
rs541673040 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46009175 | GACAGGGTTTCACCA[C/T]GATAGCCAGGCTGAT | 51317 |
rs541683281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46101919 | GCTGGAAGCAGTGGC[A/G]CAATCTCGGCTCACT | 51317 |
rs541687895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45966979 | AACGCTTTCCCCTTA[C/T]GCATGAAGCTTGACC | 51317 |
rs541709475 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46041994 | TTTAAAATCCTGTAT[A/G]TCTGTTTAAGTGTTA | 51317 |
rs541710594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46075404 | GACTCATTCATTGGC[A/G]TCTTGTCAAACTAAC | 51317 |
rs541714597 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46025076 | GTGTTCTAGAAACTT[A/T]ATGAAAATAAACACA | 51317 |
rs541741361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46084790 | GTTCACGCCATTCTC[C/T]TGCCTCAGCCTCCAG | 51317 |
rs541760977 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45961198 | TTGCTGGAATTTGCA[A/G]CTCCTGTTCTTTTTG | 51317 |
rs541767115 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45992847 | AAACAGCTTAAAGTA[C/T]CTTACATATAATTTA | 51317 |
rs541771186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46111075 | CAGGCGTGAGCCACC[A/G]CGCCTGGCCATATTA | 51317 |
rs541779585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45957375 | CTCCAGGACAGATTA[C/T]ATGTTAGGCCACAAA | 51317 |
rs541782564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46093160 | AATTTAGGTTTTGGG[A/G]TCCCAATCCAATATT | 51317 |
rs541784851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45975347 | TAAAATAAAATAAAA[C/T]AAAATAAAATAAAAT | 51317 |
rs541794950 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45936072 | CACTTGAGCCCAGGA[C/G]TTTGAGACCAGCCTG | 51317 |
rs541805152 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46043428 | ATCCTTTCTGGTTAA[C/T]ATACTACCTTCTATA | 51317 |
rs541805360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46002526 | AGCACTATTTGGGGG[A/G]AAAAAAAAGGAATTC | 51317 |
rs541817877 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45966868 | GGGATCCACCCGCCT[G/T]GGCCTCCCAGAGTGC | 51317 |
rs541834919 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46084566 | GCTCAGCACTGTGTT[A/C]ATCACTACATACTGA | 51317 |
rs541838731 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46074523 | ATTTTATTTTTTTGA[C/G]ATGGAGTCTTGCTCT | 51317 |
rs541846064 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46077853 | GTTTACCACATTAAA[C/T]AGGAAAGGACCTGTT | 51317 |
rs541872509 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46073245 | AAGTGGGAGAATGGC[A/G]TGAACCCAGGAGGCG | 51317 |
rs541888343 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45967921 | ACTCTTAATAGTTCA[G/T]ATTCTATTCTATTCA | 51317 |
rs541893128 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46042781 | TCCCCTTCTGCCATA[C/G]ATAGCACCTTCTTGC | 51317 |
rs541929164 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46026052 | GTCTCAGATCATGCC[A/G]AGTTATCTAAATATA | 51317 |
rs541943558 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46085677 | CTACTCCTTAAACCA[A/G]TACAATAAGATTCAT | 51317 |
rs541947954 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46107000 | ACACCTTTTACCAAC[C/T]GTCCTCCAGCTGTCC | 51317 |
rs541949125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | PHF21A | GRCh38.p7 | 11:46075119 | TGCCACTTGATGAAA[C/T]GTCTTAACATAGATA | 51317 |
rs541982365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45940686 | AGGGCTACTCTTTTC[C/T]TCTAGAGGGTCAGCC | 51317 |
rs541988717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46001717 | GTATGATAGGCCATG[A/G]GAGAATAAAACCAAT | 51317 |
rs542028080 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46010570 | TAAATTATATTTGGC[A/G]CCGGAGTATGCTTTT | 51317 |
rs542058230 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46005393 | ATATTTGCACAATAT[A/G]TTAACGCCTTGTATA | 51317 |
rs542063746 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45931476 | CCCTCAGCCAATCAA[A/G]CAGCCAGGGCCTAAC | 51317 |
rs542069974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46083921 | TTCTTTTTTGTTAAC[A/G]CCTTTGGTATATGAA | 51317 |
rs542101874 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46077413 | AAAAAAAGAATACTA[G/T]TTTAGATGAGATACA | 51317 |
rs542103822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45939701 | CAGGTAAGTCTGCTG[A/G]AGCCTCTGAACAGAA | 51317 |
rs542106044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46040416 | AATTCCAAAATAACT[C/T]AGCAATCTAATTATA | 51317 |
rs542110249 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46092132 | ATTTGAATAACTATC[A/C]AGCTAGCATCAGGAT | 51317 |
rs542171328 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:45953130 | CAATTGATAATATAA[A/G]TACACATTAGCTGAG | 51317 |
rs542220599 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45998073 | ATATACATGTACCAC[C/T]GTGGAGAGAGGCTAA | 51317 |
rs542224109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46071266 | ATGAATACGCCCCAG[A/G]TAGCTGCTGTCCCTT | 51317 |
rs542224177 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46080158 | TACTATATATTTATC[G/T]AACTACTAGTTTTTT | 51317 |
rs542228894 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45966426 | CTTCTAATATCTGTC[C/T]ACTTCTATCCTCACT | 51317 |
rs542259559 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46031377 | AATGTAGCTCAGATT[G/T]ATTATGTCACTTCCT | 51317 |
rs542274248 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45962179 | TATAGACATCACATG[C/T]AGCATAGCAACTGGT | 51317 |
rs542278989 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46024030 | TGTGGGAACACTGAT[A/G]TTCTAAGGAACACAG | 51317 |
rs542280455 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45981951 | TTTTCTTTTTTTTTT[C/T]TTTTTTTTTTTTTTG | 51317 |
rs542285898 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46118561 | GTACAGAAATTTTTT[A/T]ATAAACATTAGCATA | 51317 |
rs542302443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46067297 | TAACAAGTATCTGAA[A/G]AGTCTAGAGGGTAAG | 51317 |
rs542305860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45953930 | ATACGGTACAGGTTG[C/T]CCTTTCTGATTTCCA | 51317 |
rs542339812 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46062865 | CAAAGACTTGGACAT[C/G]AATGTTCAAATTAAT | 51317 |
rs542350485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46017217 | CTCAGGTGATCCGCT[C/T]GCCTCAGCCTCCCAG | 51317 |
rs542359903 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46018305 | TTTCTTATAAAAGCA[C/T]CAAAATGTACCTCCC | 51317 |
rs542373204 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46037597 | GCGGTGAGCCGAGAT[A/C]GTGCCAGCGCACTCC | 51317 |
rs542384009 | in-del | -/AAAA | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46029670 | TAGAGCCTCCGTCTC[-/AAAA]AAAAAAAAAAAAACT | 51317 |
rs542459213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46044977 | TATGGTCATTTAAGG[C/T]CTTCTAGTACCAGGT | 51317 |
rs542490467 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45974581 | ATCTCATTCTCCTGA[A/G]TACCTTGGACTAAAG | 51317 |
rs542508323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46079432 | GGTGACAGTGGCTTC[C/T]GAAAGGAATTTAAGC | 51317 |
rs542515075 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46100701 | CCCCATGCATTGAGA[C/T]GGAATAATTACACCT | 51317 |
rs542535545 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46020456 | TACATACGCAGCGGA[C/T]GGAAGTGCTTACCAG | 51317 |
rs542576936 | in-del | -/TAGCT | | | intron-variant | PHF21A | GRCh38.p7 | 11:45966458 | CACTATCTACTATCC[-/TAGCT]TATGTTTGGCTCACT | 51317 |
rs542589753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45983245 | GAAGCTTGGGGTGGG[A/G]GCTGGTGGGGGGACA | 51317 |
rs542591419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46088299 | ATCCAACAGCTCTAC[A/G]AGTCACTATCAGCAA | 51317 |
rs542593264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45984600 | GGTTCGTTTTTCCAC[C/T]GTTTAAGTCACGTTC | 51317 |
rs542601433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46021529 | TTGCACATGTGTGTG[C/T]GTGCATGTGTGTGTG | 51317 |
rs542613216 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45945685 | GGAAACTCAGAAGAA[A/G]GCTGCCTTACATGGC | 51317 |
rs542622024 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PHF21A | GRCh38.p7 | 11:45955574 | GCAGCAGTGCTTTTA[A/G]GGAAGGGCAAATCAA | 51317 |
rs542624090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46052829 | TGGACATCTCTGACC[A/G]AGCCATCTTACCAGG | 51317 |
rs542628966 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:45950431 | AGCAGGGGTGTCCAA[A/G]CTCTTGGCTTCCTTC | 51317 |
rs542638371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46004706 | ACTTTTACTGTGGAT[A/G]AGGGCTGTATCTGCC | 51317 |
rs542639880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46029750 | AGCAATAAATTTCAT[A/G]TCATTTCCAATAGTG | 51317 |
rs542643362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46013279 | AGTTTTAAACTGCAC[A/G]CTTAGAGTAGCCTGA | 51317 |
rs542661159 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46061184 | CTGTTTTTGTACCAG[C/T]ACCATGCTGTTTTGG | 51317 |
rs542711383 | in-del | -/CT | | | intron-variant | PHF21A | GRCh38.p7 | 11:45993706 | AGATACAGTCAACTG[-/CT]CCAGGAAACAGAGTC | 51317 |
rs542718745 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46006803 | AAAATATTTTAAGAC[C/G]AACAACCCTCCCTTG | 51317 |
rs542755718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46013765 | CTGTACTGAATACCA[C/T]AGGTAACAATGGTAA | 51317 |
rs542770648 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46041721 | TTTCAAACATACATA[A/G]AAGTTCATAGTATAG | 51317 |
rs542801797 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45995774 | CATATTCAGCTCAAT[C/T]ATACATGTGTAGACA | 51317 |
rs542812319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45960497 | GAACAGGTACATCTA[C/T]GGAGACAGAAAGCAG | 51317 |
rs542839763 | in-del | -/TTC | | | intron-variant | PHF21A | GRCh38.p7 | 11:46086616 | GATTATGTATTACAG[-/TTC]TTCTTGAAAACAACA | 51317 |
rs542847694 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45978080 | GCCGAGGCGGGCAGA[A/C/T]CACGAGGTCAGGAGT | 51317 |
rs542848284 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46048585 | GACCAGCCTGGCCAA[C/T]ATGGTGAAACCCCAT | 51317 |
rs542863808 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45988110 | GGAACACTGCTCAGA[A/C]AAAACAAATTGTTTT | 51317 |
rs542882712 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46011994 | ATCACCTTCTTTACT[G/T]CCTGTCCATCCTGGG | 51317 |
rs542905840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46088952 | TACTGCTAAGAAATA[C/T]TTTGCTGTTACTGAG | 51317 |
rs542921448 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:46011424 | AGCCCAGTAGGTGGA[A/G]GTTGCAGCAGTGAGC | 51317 |
rs542928761 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46122191 | AGCGGCCCCAACTCC[C/T]TCCAGTGCAACAGCA | 51317 |
rs542951452 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46115663 | TCATTAATATTTCCC[A/T]GCACAAAATAATATG | 51317 |
rs542986458 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45978712 | TCTATAGCTTTCAAC[A/T]GAGTCATAAAGGGAT | 51317 |
rs543017058 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45943795 | AGATGAAAGTTAACA[A/T]CACCAACAACAGAAG | 51317 |
rs543050172 | in-del | -/A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45977843 | TTTTTCTTCTTCTTC[-/A/T]TTTTTTTTTTTTTGG | 51317 |
rs543067136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45996745 | AAACAAAAGGTAGCT[A/G]TATTTATAACTCTGC | 51317 |
rs543069415 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46095911 | CATTCAAAGACACTT[C/T]AAAATGTCACCTTAC | 51317 |
rs543071893 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46075742 | CATTAATGATTCATA[C/T]CTCTTCCACATAATT | 51317 |
rs543078270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45951830 | TTTTTTTTTTGAGGC[A/G]GAGTCTCACTCTGTC | 51317 |
rs543078640 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | PHF21A | GRCh38.p7 | 11:45943103 | CTTCCAAGCTATCAT[A/C]ATCATCATCTTTCTT | 51317 |
rs543087739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46053466 | GTATAAATGAAATCA[C/T]TCTTAAGAGGATATT | 51317 |
rs543102898 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45987496 | GAAACTCCGTCTCTA[A/C]TAAAAATACAAAAAA | 51317 |
rs543104560 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46047966 | AAATGAAATATGTAA[C/T]ACTTTTTTAAACAGA | 51317 |
rs543121072 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PHF21A | GRCh38.p7 | 11:45945372 | ACTCTGCTCTAAAGA[A/G]CAGAGTTTCTGCTCA | 51317 |
rs543191947 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46113414 | TCTTACGTAGGAGAA[C/G]CACAGAAAAAAATGC | 51317 |
rs543214781 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46044125 | TAGAATCAAGTTTCA[A/C]CCTAAGCACTACTGT | 51317 |
rs543229357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46103687 | AAATTCTTGCTAAGG[A/G]TAACATATACCATAT | 51317 |
rs543257773 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45949695 | CTGTCCTACACGTGG[C/T]TCTCTGTTGAGAGTT | 51317 |
rs543258638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45934520 | CAAACCGGCAGAGCC[A/G]CCATCAGACTTCCAA | 51317 |
rs543268675 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46118598 | CACAAAATTTCCTCT[C/T]TGCCATGAAAAGATA | 51317 |
rs543301742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45961255 | GCACAAACCTAGAAT[A/G]AAGTTAATCAAGTAT | 51317 |
rs543329788 | in-del | -/GT | 0.00159617 | 0.0282053 | intron-variant, utr-variant-5-prime | PHF21A | GRCh38.p7 | 11:46049450 | GTGTATTCCTGTACA[-/GT]GGCATCTGCAAGCCA | 51317 |
rs543335087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46069945 | AACTCCATGCACTCA[A/G]TGGATACACGTGCAT | 51317 |
rs543335617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45978023 | ACAGAGATGGTGGGC[C/T]GGTTGCGGTGGCTCA | 51317 |
rs543340913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45951122 | CTTTTCTTTGCTTGC[A/G]TGTGGTCTGAAAAGT | 51317 |
rs543346610 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46120399 | CCCCCGCCCCCGCCC[G/T]CAGCCCCCGGCCGGC | 51317 |
rs543365810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45970665 | TAAAGTGCCTCAACT[A/G]ACTCCAGTTCTTTCT | 51317 |
rs543371259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46078074 | CCCATCACCATGCCT[A/G]GCTAATTTTTGTATC | 51317 |
rs543374951 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46059989 | CCTCAGGTGATCCAC[C/G]CACCTCGGCCTCCAA | 51317 |
rs543376282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46036603 | TAAGTAAAAGTAAAG[A/G]TACAGGTATACATTT | 51317 |
rs543390817 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46095544 | TGTCATACAATTTTT[G/T]GCAAACGGAAGATTG | 51317 |
rs543425508 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45950889 | TATACTGCCACAATG[C/T]TAACTCACAGCTAAA | 51317 |
rs543427132 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45978602 | GGTGTTGGTTGTAAG[A/C]GGTATCCACGCTTAG | 51317 |
rs543431164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46037587 | CGCCTCTGTTGCGGT[A/G]AGCCGAGATCGTGCC | 51317 |
rs543431847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46011404 | TGAGGCAGGAGAATC[A/G]CCTGAGCCCAGTAGG | 51317 |
rs543454321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46068915 | ACTCAGGTAAAATGC[C/T]CTATAATAATGTGGC | 51317 |
rs543487281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46060927 | GAGGTTATCTACCAG[A/G]GTTTTTATAGTTTTG | 51317 |
rs543487344 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46051631 | ACCAGCTGTTTTTAA[C/G]CATGCCAATGTGCAA | 51317 |
rs543523856 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45973969 | ATTCTACAAAATACT[A/G]ACTAAAGCCTCAAAC | 51317 |
rs543550749 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45970454 | AGCTCTTAGGTGCCA[C/T]TTTAAGGGAATTTTA | 51317 |
rs543561876 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45942977 | TTTCTAGTCAGTTAG[G/T]CCAAAAACTTTGGTT | 51317 |
rs543584711 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45967633 | GACAGCTGTAGGGAC[C/T]GCTGTATGGACTCAT | 51317 |
rs543590286 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46088322 | ATCAGCAAGGCCACT[C/T]GCCTAGCCCAAAATA | 51317 |
rs543599802 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46025972 | AACACTGATACAATA[A/C]TATTATCTCCAGACT | 51317 |
rs543609373 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45953742 | ATATTCAAATGTGGA[A/G]CATATTAATAAAAAG | 51317 |
rs543651351 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46081931 | CTGTGTGTCCCTTTA[A/C]AAAAAAATTTGCTAA | 51317 |
rs543657008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46096623 | TTCCCAACTCTCTGG[C/T]TACTCTCTTTGGTTT | 51317 |
rs543658097 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45986233 | CCTTTTATTTGCTAG[C/G]CTGATTGAAATGCAG | 51317 |
rs543672581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46018742 | TCAAGAAAACAGAGA[C/T]AGCAATTGATAGTTG | 51317 |
rs543678012 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46031946 | CCACACAGTTACCCA[A/G]TTTTCCCCAATGCAC | 51317 |
rs543680012 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46034427 | TTATCCTCTTATGTT[A/T]TTAGGTCCTTTCCTG | 51317 |
rs543701313 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930631 | GTTACCAGGATGCAG[C/T]GCCTGGACAGGAGCT | 51317 |
rs543704333 | in-del | -/T | | | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46086123 | GTTTTAGCTACTATC[-/T]TTTTTTTTTTTTTGA | 51317 |
rs543748216 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46076928 | AAGCAACCCGAAGCA[C/T]TTAGCCAATCAAATC | 51317 |
rs543768715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45987428 | GCACTTTGGGAGGCC[A/G]AGGTGGGCGAATCAC | 51317 |
rs543771485 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46056308 | GGGATTCAGAGAGTA[A/G]AACAGACTTTACATT | 51317 |
rs543805706 | in-del | -/TGTTGTTGTTAGTATTAT | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:46033255 | ACTGATTCCATTTTC[-/TGTTGTTGTTAGTATTAT]TGTTGTTGTTGAGGC | 51317 |
rs543809793 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45960492 | ATCCAGAACAGGTAC[A/G]TCTATGGAGACAGAA | 51317 |
rs543832540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45949789 | GGATGAGCTTTATCC[A/G]TAAGACTTAAACTGA | 51317 |
rs543852881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46004600 | TAAAAGTTTTAAAGA[A/G]CTGTGCTCATTTGAC | 51317 |
rs543890174 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45994797 | GTTCCAGTAGTAGGA[C/T]GACTTTGCAATATTC | 51317 |
rs543901315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46112595 | CTACATTTTCAAGTA[C/T]TAAATTTACACTAAA | 51317 |
rs543935665 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46099914 | TAAAAACTAAAAATG[G/T]TTCCATACAATTTAC | 51317 |
rs543941906 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45958288 | CAAAGACACCAAAGA[A/G]TAGAAAATGGGCTGG | 51317 |
rs543981439 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46121999 | GCGGCGGCGGTGATG[G/T]GGCCGAGCACCGAGC | 51317 |
rs544000342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46022469 | CTTAAAAAAAAAGAA[A/G]AAGAAACAAAAAGAC | 51317 |
rs544023073 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46056767 | AGACCCTTAGAGAGG[G/T]AAACTTTAAGATTAG | 51317 |
rs544034489 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46062828 | GGCATTTACTGAAGA[G/T]AAATGAAAGCAGATC | 51317 |
rs544039078 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46102688 | TTTCTGAGGTAAAAA[A/G]GTATTTTTCTATTCT | 51317 |
rs544039116 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46064005 | TCAGAAAAACAAATT[A/T]CAAGTTCTGTCGATT | 51317 |
rs544048155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46085493 | TGAATGTGGCCTTAG[A/G]CATGATTTTAGGTAC | 51317 |
rs544060256 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46010693 | AGCCAGCGTGCAAAG[C/T]CTTGACCCACAGAAG | 51317 |
rs544073759 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46015123 | GCATTTTTTCATGTT[G/T]GTTGACTGCTTGTAT | 51317 |
rs544075765 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46099326 | AAGAAAACTCCTGCT[A/G]CATCGATAGCCAAGA | 51317 |
rs544082401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46068388 | CATACATATATATAA[C/T]ATATGCACATTATTT | 51317 |
rs544109623 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46014474 | GTGGCAATGAACATA[A/C]AAGTGCAAGTGTACT | 51317 |
rs544110968 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46023058 | GCCCGGCCTTGTTAT[C/T]TTCTATTATAGTATA | 51317 |
rs544120597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46076249 | TAATAACATTTCACC[A/G]AAGTTTTTTCACGTA | 51317 |
rs544127041 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45959693 | AATTCAGCAAAGTTG[A/T]AGGGTACAAGATCAA | 51317 |
rs544127182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45968354 | GCCTACAAGGTTCCA[C/T]CAGCTCTGGCCCTAG | 51317 |
rs544157615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46086354 | TTGATCTCCTGACCT[C/T]GTGATCCGCCCGTCC | 51317 |
rs544165912 | in-del | -/AAAAAAT | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45989992 | GTGAGACCCTGACTC[-/AAAAAAT]AAATAAATAAAATTA | 51317 |
rs544168577 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PHF21A | GRCh38.p7 | 11:45961072 | ATTAAGAATAAAAGC[A/G]GGATATCTGTTATAC | 51317 |
rs544169180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45947243 | ATCTAAGTCAGGGCC[C/T]TTGTCTTCTAGGGGC | 51317 |
rs544171267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46064201 | CATTCACTGTTCATA[A/G]GGAAAATTAAGTTCA | 51317 |
rs544178629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46106590 | TTTGCACATATCCAA[C/T]TCCATCCACTGATAA | 51317 |
rs544179424 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46074796 | GCGTGAGCCACCGTG[A/C]CTGGCCAATAAAACT | 51317 |
rs544209491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46072958 | TATCAGAATATCTCC[A/G]TAAAAGATCACATAT | 51317 |
rs544216978 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45989053 | GACAAGACACCCCTC[C/G]TCAAACAACAGGGAG | 51317 |
rs544256086 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45956007 | CAGACCAGAAGGAAA[C/T]GGGTTAATATATTTA | 51317 |
rs544258755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46097513 | TCTACAGCAGTTTCA[A/G]GAGCAAAAGAATACT | 51317 |
rs544286672 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46108718 | GCTTTTGTAATATTT[A/C]TTGAAAGGACACTTA | 51317 |
rs544306544 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45938935 | GCCTCCCAGGTTCAC[A/G]CCATTCTCCTGCCTC | 51317 |
rs544325298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46107867 | TTTTTTTTTAACTGC[A/G]TTAAAAAATACTGAG | 51317 |
rs544329798 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45989875 | ATGGTGGCATACACC[A/G]GCAGTATCAGCTACT | 51317 |
rs544338775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45999582 | GGAAATTTAAAAATA[C/T]ATCTATAGAGGACAA | 51317 |
rs544372949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45953859 | ATGAATCTATAAATA[C/T]GAGTCTAAATAAGGT | 51317 |
rs544379349 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:45964130 | TTGAACCTGGGAGGC[A/G]GAGGTTGCAGTGAGC | 51317 |
rs544417743 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45972839 | GAATTGCTTGAACCC[A/G]GGAGGCGGAGGTTGC | 51317 |
rs544440635 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45953077 | TGGGGTTCTAATGTA[A/C]TACAATGGTTGTAAC | 51317 |
rs544447672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45944762 | ATGCCCTTAAATCCA[C/T]TCCATTTTTGATCTC | 51317 |
rs544457891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46005957 | AAACATACAATTTTA[A/G]AAGTTTATTTGGAGC | 51317 |
rs544459231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45998483 | TTTTAGGAAACAGAA[A/G]ATGTACATGCAAAAT | 51317 |
rs544505984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46114541 | AGTGACGGGCTACTA[C/T]AAAGGATTTGAAGCT | 51317 |
rs544531480 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46020649 | AATATGAACATGACC[C/T]AGAGTTCTCTATATT | 51317 |
rs544541597 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46105715 | GAAAAAAGCAAAATT[A/C]TCATAATTTTGTAAC | 51317 |
rs544548707 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46082258 | CTCAATTTCAGCCCT[A/T]ATCTCATTCCCTAAC | 51317 |
rs544579728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46063786 | CAGGAACTGATGAGG[C/T]TTAGGGGCAGCACTT | 51317 |
rs544600962 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46045327 | TATTATACCAGGTAC[C/T]AACACAAAGGAGAGG | 51317 |
rs544638100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45936975 | CTCAATTTTAGATTT[C/T]GATGTCCCTCAAAGA | 51317 |
rs544652953 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46091477 | TGCCCCACAATTACA[C/T]TTCTCTCTCTTTTTC | 51317 |
rs544663480 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46022982 | TCTCGAACTCCTGAT[C/T]TCAGGTGATCTGTCT | 51317 |
rs544663577 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45984944 | TCCATGAATCAACAT[A/G]CAATTTAAAAATACA | 51317 |
rs544669205 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46089816 | GGAGGGGGTGGGGGG[A/C]GGGTCCTCATTTTTT | 51317 |
rs544676843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45980896 | TGTGGCGGTACACAC[A/G]TTTGTTTAGGCAGAG | 51317 |
rs544696638 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45978156 | AATACAAAAATTAGC[C/T]GGGCATGGTGGCACG | 51317 |
rs544736767 | snp | G/T | 0.00755907 | 0.0610114 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930789 | TCTCAAAAGTGGCTG[G/T]CAGAGCAGCTAAATT | 51317 |
rs544743955 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46106795 | TCTCAATGGGAGTAG[A/C]AGCTATCAGGGCAGG | 51317 |
rs544756769 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46062812 | AACCCAGACATACTA[A/C]GGCATTTACTGAAGA | 51317 |
rs544756905 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46089147 | TATATTCTCAGACAC[A/C]ATGTTTAAAGTAGGT | 51317 |
rs544790471 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45996932 | CAAATGTATCCATTG[C/T]AAATGTTAGTCTATG | 51317 |
rs544790966 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46071803 | CATGATATAGCCAAT[G/T]ATGCTAATATTTAAA | 51317 |
rs544829231 | in-del | -/AAG | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46099040 | ATTTTAAAAATAAAC[-/AAG]AAGAAGTTAAACTAA | 51317 |
rs544850086 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46059067 | AAGCTAGTTGGAGTT[-/A]AGATTCTACTATACA | 51317 |
rs544851815 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46014413 | TATCCAATCCACTGT[C/T]GATGGACACCTAGGT | 51317 |
rs544896923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45945354 | GGAACCTGTTTCTGA[C/T]CAACTCTGCTCTAAA | 51317 |
rs544907190 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46095073 | AATGAGGTTCACATA[C/T]CCAAAAAGAGGAAAT | 51317 |
rs544908339 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46030392 | ATGATTTGCCCAGGT[C/T]TTCATCATTTGTCTT | 51317 |
rs544938060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46013852 | CGAAAGATGAAAAAC[A/G]GTAAACCAGCTTGCA | 51317 |
rs544971236 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45957780 | AAAAAGAAAAAAGAA[A/G]ATAAAGTCTAGGATG | 51317 |
rs544972967 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46072064 | AAATAAAACAAACAC[A/G]TTCCCTGACTTCCTG | 51317 |
rs544981029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46021575 | TCAGAGACAGGGTCT[C/T]ACCCTGTCATCCAGT | 51317 |
rs545004623 | in-del | -/CTTTTGCC | 0.0146672 | 0.084371 | intron-variant, downstream-variant-500B | PHF21A | GRCh38.p7 | 11:45934803 | CCGGGGACTTAGAGT[-/CTTTTGCC]CTTTTGCCCTCAGCT | 51317 |
rs545027353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46045141 | CTGACTTAGAATGCC[C/T]CCATTCTTTCTGTTT | 51317 |
rs545055327 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46104727 | AAGATTTCCTCATTT[G/T]ATTGTCACATGAACC | 51317 |
rs545077671 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45998985 | GCACCTGCCACCACG[C/T]CTGGCTAATTTTTAT | 51317 |
rs545092016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46116456 | AAGAATCAGGGAACT[C/T]ACATACTCACTAAAA | 51317 |
rs545119034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46053548 | ATATATATAATTATA[C/T]GTATACCATGACTGG | 51317 |
rs545140584 | in-del | -/G | 0.00279162 | 0.0372561 | intron-variant | PHF21A | GRCh38.p7 | 11:45959094 | ATCCCAAGAGTGGAA[-/G]GGTGGTTCAATGTAA | 51317 |
rs545153484 | snp | A/C | | | intron-variant, downstream-variant-500B | PHF21A | GRCh38.p7 | 11:45934921 | TGAGGAGGAGAAAGC[A/C]GGTAAGCAGGACAGT | 51317 |
rs545163175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46007334 | CTTTTTTTTTTTTTC[A/G]AGATGGAGTTTCACT | 51317 |
rs545191358 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46019813 | GCAACACAGAAGCAA[A/G]TAAGAAATATTACAT | 51317 |
rs545227875 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930190 | CAAGGGAGGCTCTGA[G/T]GGCCCCAAGAGAGAA | 51317 |
rs545245216 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46089045 | TAAGTCCATGACACA[A/G]TGTGCCCCAAACTGT | 51317 |
rs545256236 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46022384 | CACTTTAGCCCAGGA[A/G]ATTGAGGCTGCAGTG | 51317 |
rs545259668 | in-del | -/CT | | | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46120337 | GGAGCCCCAGCTACC[-/CT]TCCCCGGCCGAGGGA | 51317 |
rs545284724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45961279 | CAAGTATACTTTATA[C/T]ACTTGTCTGCATGAA | 51317 |
rs545286809 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46080983 | CTACTATTCTAACAA[C/T]CCTGAAACCCAGCTC | 51317 |
rs545300091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45972712 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 51317 |
rs545300363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45963010 | AAGCTCTATCAACGT[A/G]AAGGCCACGACAGGA | 51317 |
rs545333264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46004936 | AACAGATAAGCACTA[C/T]ACAACAAAGTTTACT | 51317 |
rs545346056 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46113497 | TTTAAAGTTTGAATG[A/C/G]ATCCATTTCAACATT | 51317 |
rs545355802 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46089682 | ATACTATTAAATTAT[A/T]TTTAATAATGTTGTT | 51317 |
rs545360091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45972134 | CAAAGATGCAATGAA[A/G]CATGACAAGGTGAAA | 51317 |
rs545388261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45935926 | GTATGCTAAAACTGT[C/T]AGTGGCTTGGGTCTG | 51317 |
rs545409884 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45992806 | AAATGGTAGTAATAC[A/G]TTTCATAATGGTGCC | 51317 |
rs545449944 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45944675 | GTTCCCTCTGCCTGG[C/G]AGGCTCTTCCCCCAG | 51317 |
rs545454991 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46116197 | TATTTTTACACAAAA[A/C]TATTTCAGTGCACTC | 51317 |
rs545460500 | snp | C/G | | | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46118843 | AAAAAAGGAAGGAGG[C/G]GGCCAGTCTTCAAAG | 51317 |
rs545461714 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46110907 | TCTCCTGCCTCAGCC[A/T]CCCGAGTAGCTGGGA | 51317 |
rs545464213 | snp | C/T | 0.000135058 | 0.0082165 | downstream-variant-500B, utr-variant-3-prime, missense | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45928857 | CTGAGGCTGGGCCGG[C/T]GCTGCCCCTCATCTT | 51317 |
rs545476598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46097489 | CACTCCCTCAAATTA[C/T]TGAGGAAATCTACAG | 51317 |
rs545499674 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46045620 | GCACTACAATGTATT[A/C]AAAAAAAGAATGGTT | 51317 |
rs545525744 | snp | C/T | 0.00103744 | 0.0227518 | intron-variant | PHF21A | GRCh38.p7 | 11:45949368 | TAAATAAAACTGGAA[C/T]ATGAGGGAAGGGCCA | 51317 |
rs545528391 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46105499 | TAACCAGGAACTGCA[A/C]GAAATGGGCAATTCA | 51317 |
rs545536170 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45961978 | GTAGATAAGGAAGTT[C/G]GTTATGTCTGACAGG | 51317 |
rs545560556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46096982 | AATCCTAAAAGTCAT[C/T]TTAAGACTCTTCTTT | 51317 |
rs545562842 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46020611 | TCGGTCCTATTTAGC[G/T]CTATAAGTTATGAAA | 51317 |
rs545565697 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45984799 | GTCTCTGCTTTTTCA[C/T]ACATTCAGTCACTCC | 51317 |
rs545570500 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46042235 | ACATGACAAAACATA[-/T]TTCCTCAATAAGGCA | 51317 |
rs545595653 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46079266 | TTTTAAGTTAACACA[A/C]AAAAAAGAGCAACAC | 51317 |
rs545629813 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46070116 | TCCTTTGTTTCAGTT[A/T]CCTAATTAGCTTAAA | 51317 |
rs545650852 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46091176 | AAAAGGAAACCTTGG[C/T]CAAATATCTACTATA | 51317 |
rs545653291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46067197 | GTAAGGGGGTCTGCC[A/G]GAAGAAAGGTATAAG | 51317 |
rs545655370 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46017129 | GCATGTGCCACCACA[A/C]CCAGCTAATTTTTGT | 51317 |
rs545680309 | in-del | -/A | 0.00636936 | 0.0560724 | intron-variant | PHF21A | GRCh38.p7 | 11:46069982 | CTCAATGCATAATCC[-/A]AACATTCCACGAATA | 51317 |
rs545690044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46074944 | GTTCCATCAAGAAGG[C/T]TGTTTTAACAGTTAA | 51317 |
rs545696480 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46038128 | TTCTCTCTCTCTCTC[-/T]TTTTTTTTTTTAAAT | 51317 |
rs545733820 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46000915 | ACAAAAGTGAACCTC[C/T]GTCTCAAAAAAATAA | 51317 |
rs545734519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46042073 | ACATTTTCTGGAACA[C/T]AACCATTGTCTATAG | 51317 |
rs545737927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46118390 | ACTGTAAATACTATT[A/G]TGTTACCAAAAGCAA | 51317 |
rs545777184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46050408 | CTGACTGTGAGCATG[C/T]TGGGGAGAGCAGGAG | 51317 |
rs545779564 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46070520 | ATTTTTAGTAGAGAC[A/G]GGGTTTCGCCATGTT | 51317 |
rs545783367 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PHF21A | GRCh38.p7 | 11:45933437 | CCAGCCACTCCCCTT[C/T]CCTCTTCTGGGCACT | 51317 |
rs545817095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46009715 | TCCAACTTGGGCAGT[C/T]TGGCTACAGAGCCCA | 51317 |
rs545818066 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45973517 | TTCTCTTTGCCATTG[A/C]CTCCTTAAATGTGAA | 51317 |
rs545819681 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46064262 | GGTCAAAATGATACA[A/G]TTTGTTTGGGCAAAG | 51317 |
rs545839497 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45974489 | GACAGGGTCTTGCTC[G/T]GTCACCCAGGCTAGA | 51317 |
rs545848202 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46105982 | AGGCACGGATTTAAT[A/T]TTTGTATACTAACAT | 51317 |
rs545864427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46049958 | TCAGACCTGTGATTA[A/G]CTCAATCAAAGTAGG | 51317 |
rs545870503 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PHF21A | GRCh38.p7 | 11:46093279 | TTCCTTTTGCCTTAA[A/G]TATGGTGTTTGTTGA | 51317 |
rs545892554 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46082653 | AACTATATCCCTTTT[C/G]AGTCAACAAATGTAA | 51317 |
rs545902634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45983156 | AATCAGAACCAGAAT[C/T]AGGAGCGTGGGAGTC | 51317 |
rs545904756 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46041023 | CTAGATTTGAACATG[A/C]CTCTACAGTAAATAG | 51317 |
rs545908883 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46066482 | GAGTCAGAAGGATCA[C/T]TTGCCAGGAATTCAA | 51317 |
rs545922097 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46083649 | TACTCTGTTTACATA[A/C]CAAATTTTAATTATG | 51317 |
rs545930954 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45984259 | CTTCTTAATATATTT[A/C]TATAAACAATAAGCC | 51317 |
rs545955481 | snp | C/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930888 | GTGTCACGAGCGTAT[C/G]TCTCAGGTGGTCACA | 51317 |
rs545962664 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46092446 | ACTTTTCCATAGTTT[A/T]TCAAGACAAGCAAAA | 51317 |
rs545969957 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46106066 | AACCTGACACAATGA[A/C]AACAGGAACTATTGC | 51317 |
rs545978083 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46087608 | GAGACTGGTCTGTGC[A/G]GAAAGAAACAAATTA | 51317 |
rs545983257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46057441 | CCCAGAGCATTAGGG[C/T]TTAATTTTCCCAATG | 51317 |
rs545992015 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46082770 | ATTCAGAATATGAAA[C/T]AAAATATTTAGTAAT | 51317 |
rs546014169 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45957216 | TATCCCTCTTTAAGT[A/C]ATGGATAAAACTTGT | 51317 |
rs546016534 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45938090 | ATTTCCCCGGGAAAG[G/T]AATTCCTCCTGATGG | 51317 |
rs546035312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46056162 | CTCCGGTTTTGAATT[C/T]CATCTTATAAGGAGA | 51317 |
rs546043143 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46090977 | TTCTCTAAGATTCCA[C/T]CCCATGTCAAAGTAA | 51317 |
rs546044809 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PHF21A | GRCh38.p7 | 11:46110042 | ACTAATTTTTTGGTT[A/C]TAACTCATTATTTAA | 51317 |
rs546064421 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45966302 | AGACTCATCAATTTC[C/T]TCTTCCAATCTTCTC | 51317 |
rs546092368 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45931305 | CCCCCAGATGGGCCC[A/T]GACAAGTTGAGGGGA | 51317 |
rs546105387 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46058330 | GCTTAACTGTGTCAC[A/C]TTGTTGGTAAAACGA | 51317 |
rs546118994 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46031663 | TTCTCTTTAGATTAA[C/T]AGGCGCTCCGAGGCA | 51317 |
rs546119915 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PHF21A | GRCh38.p7 | 11:46047286 | TTAGTGAAAAGTGAC[A/G]TAAGTGGTTACTATT | 51317 |
rs546127682 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45939880 | GATAAGAACACCAGG[A/G]AAGGGAAGACTGAAG | 51317 |
rs546136163 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46100270 | CCATTAACCTTGTTT[A/T]AAAAAAAAAAAATCC | 51317 |
rs546208826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46023287 | AGAGAGACAGCTGAT[A/G]GCTAATTACTGAGGC | 51317 |
rs546214756 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46030622 | AAATTCAAAAAGATT[A/C]TTTAATCCTAAAACA | 51317 |
rs546231075 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46061943 | GGACTTGATCAAGAG[A/T]TGGGTTGGGTATAGA | 51317 |
rs546237617 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46027206 | ATTATATTTCAAAGA[C/T]GATGCACTGATTTCT | 51317 |
rs546257420 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46102103 | CCTTGTGATCCACCC[A/G]CCTCGGCCTCCCAAA | 51317 |
rs546262307 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46090330 | ATAATGCAAGTGGGT[A/G]TGGTAGTCTCAGCAT | 51317 |
rs546264721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45991088 | CTTTTTACTGCCTCC[A/G]TAGTTCTACCCTTTC | 51317 |
rs546319825 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46100039 | GTCAATGAGAAGTGG[A/G]AACAGCTACAATACA | 51317 |
rs546321063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46023981 | AAACAAAAAGAATCA[C/T]TGAATGGCATAGAGC | 51317 |
rs546330490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46048052 | CAATGGCTTTTAACA[C/T]ATTCACAGTTGCACA | 51317 |
rs546359136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46107729 | TCACTAATAATCTCA[A/G]CAACAAGTTAAAACT | 51317 |
rs546362968 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45929565 | ACCTCTGGCCTGCCC[A/G]TCCCATCCCGCCTGA | 51317 |
rs546392495 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46044327 | AGAAAATTCATGCAA[A/G]GTAAAAGAAGTAATT | 51317 |
rs546423550 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46012526 | CTATTTGGTCTTACG[-/C]CAAGTTAACTCACGA | 51317 |
rs546454590 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45998754 | GGACCTCAAGTCATC[A/C]ACCTACCTCGGCTTC | 51317 |
rs546459925 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46028846 | CAAAGTGCTGGGATT[-/A]CAGGCGTGAGCCACC | 51317 |
rs546473270 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45998544 | TTAAACAGAGTTTTG[C/T]TCTTGTTGCCCAGGC | 51317 |
rs546476833 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45997552 | AGATCCAGTGACAAT[C/T]AGATTTCTCCTCTGC | 51317 |
rs546487493 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46055158 | TTGAAGCAATCTGAA[C/T]GTAGAATCCTTCTGG | 51317 |
rs546496698 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46025701 | AAATTCCCCAAAAAT[A/G]TTATCTTTACCACAT | 51317 |
rs546506421 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45974895 | ACCCAAATTGCATGA[A/G]CTAGAAGTTAATGCA | 51317 |
rs546508042 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46114914 | TTCTGTGTTTAAGTT[A/G]TTTTTCCCCTAGGCC | 51317 |
rs546590734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45972202 | GATGAACTGAGGTGA[A/G]AGGACTTGACTGATG | 51317 |
rs546603369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46099941 | TTACATTTTTTAAAA[A/G]ATCTTTGTAGTCCAA | 51317 |
rs546607339 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45981988 | TTGAAACAGGGTCTG[A/G]CTCTGTCACCCAGGC | 51317 |
rs546621414 | in-del | -/AA/AACAAA/AAG | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46088420 | AATAACAACAACAAC[-/AA/AACAAA/AAG]AACAACAACAACAAC | 51317 |
rs546635273 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | PHF21A | GRCh38.p7 | 11:46083184 | AAAAAAAAAAAAAAG[G/T]ACACAGCTTATTACC | 51317 |
rs546644304 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45939063 | GGTCTCGATCTCCTG[A/T]CCTGGCTATCTGCCT | 51317 |
rs546653895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46007129 | CCAACCAACCATAAC[A/G]TGACGAGACATCTAT | 51317 |
rs546659858 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46107185 | TTTGACAACATGCAT[-/A]AAACACTAGTTTAGA | 51317 |
rs546699747 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45939998 | TGTGCACAAGAAGCA[A/G]TAATAGAGAGGAATG | 51317 |
rs546720884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46091258 | TTTTAAAAAGGAGTA[A/G]TCTTGCACTAGGCGA | 51317 |
rs546743760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45973237 | ACTGGACAGTGGAGA[C/T]AGACGGTATTTCCAA | 51317 |
rs546748920 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46018615 | ACCTATTTGACTCAA[C/T]TTCATATGGAAGAGA | 51317 |
rs546768224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45946665 | CAGGTGTGAGCCACC[A/G]CACCTGGCCGAATTT | 51317 |
rs546768524 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45937674 | TTAGTAGAGATGGGG[A/T]TTCGCCATGTTGGCC | 51317 |
rs546772207 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46097152 | AGCCTCCTAACTGGC[C/G]TCCCCAATTCTACCC | 51317 |
rs546814977 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45958989 | TAAATGAAAAACCCT[C/G]AACAACAACAAAAAT | 51317 |
rs546848495 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45990618 | GATTCATGCTTTTAC[G/T]GTATTGTTCTCCAGT | 51317 |
rs546855624 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45971624 | TAGTAATAACTGCAG[A/T]CTAATTCAGGCACAG | 51317 |
rs546868938 | in-del | -/T | 0.320168 | 0.239951 | intron-variant | PHF21A | GRCh38.p7 | 11:46016972 | ATGTTTAACCTGGAT[-/T]TTTTTTTTTTTTAAT | 51317 |
rs546886839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46107971 | CACATGAAGTTGTGA[A/G]GACCAGGACTAATTC | 51317 |
rs546887174 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46098990 | CAAGATAATTCAAAT[A/G]AAAGTCACTAAGAAA | 51317 |
rs546906206 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B, utr-variant-3-prime | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45929081 | CCCTTTTTCATAATT[A/G]AAGTTTTAAAACATC | 51317 |
rs546916873 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45979142 | CTGCCTCAGCCTGCC[A/C/G]AGTAGCTGGGATTAC | 51317 |
rs546963349 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46021951 | GGAACAGAAAATACA[C/G]GCATTGCACTAGTAG | 51317 |
rs546971407 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45985495 | TTAATGCAAGTAAAA[C/T]TCAATAAGAGAATCT | 51317 |
rs546994224 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46029458 | ACGGGGAGGCCAAGG[A/C]GGGCAGATCACTTGA | 51317 |
rs547001554 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46030123 | AACGCTAAACAATAG[A/G]GCAAACTGCTGACTC | 51317 |
rs547023039 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46088799 | TATATCTAGAAGACT[A/G]TAGGCTTTTCTGTTC | 51317 |
rs547089940 | in-del | -/AACAGAGTTACAAA | 0.00478085 | 0.0486577 | intron-variant | PHF21A | GRCh38.p7 | 11:46033799 | TGTTTACTTTTTTGT[-/AACAGAGTTACAAA]AGGTGGCTGCTAGAA | 51317 |
rs547100362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46076445 | GATTCTCTATCACCT[A/G]TTCTCACTAACTGCC | 51317 |
rs547109436 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PHF21A | GRCh38.p7 | 11:45963345 | GAATTGTTTGAATCC[A/G]GGAGGTGGAGGTTGC | 51317 |
rs547113917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46063269 | GTACATACAGTCTAT[A/G]TACAGTGTAGCACTC | 51317 |
rs547133986 | snp | C/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45929646 | GTCCAAAGGCTGCTG[C/G]GGAAGGGGTAGGGGG | 51317 |
rs547169314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46092821 | CAAGTGCAGTGGCAC[A/G]ATCACAGCTCACTGC | 51317 |
rs547171266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46038058 | CTAATTCACCTTCTT[A/G]CAGAGCCCATTTTGT | 51317 |
rs547199339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45936099 | CCTGGGTGACATGGC[A/G]AAACCTGTCTCCACC | 51317 |
rs547222033 | snp | C/G | 0.00014929 | 0.00863844 | intron-variant | PHF21A | GRCh38.p7 | 11:45946127 | GGAAGTGAGGTAGCA[C/G]ACAGAAGGTTAATTC | 51317 |
rs547229356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46089262 | ATATCAGGTTTCAAT[C/T]TGTACAAAATACTTC | 51317 |
rs547253329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45967281 | GCTGAGACATAAGGA[C/T]TGCTTGAACCTGGGA | 51317 |
rs547258534 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45935399 | CTGAAAATCCTCTCT[A/C]TGATTAAAGCCAAGA | 51317 |
rs547273195 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45975869 | CTCTTAGCATCTCCC[C/G]CTGGCCCCCCGATTG | 51317 |
rs547286655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45984475 | AAGACAGGTAGTCAC[A/G]GTGATCAATATTGTG | 51317 |
rs547335507 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46038498 | CTAGGTTCTTGAAGG[A/C]GGTAAAGGAGTCAGT | 51317 |
rs547335771 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46006335 | ATTCTTAATCTTTCG[A/G]TTGTATATACAATTA | 51317 |
rs547344083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45940126 | GTAATCCACTAGGGT[A/G]TCTGGCAGCCCAGAA | 51317 |
rs547358876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46058734 | TAGCCATGTCTGTAC[C/T]AGTAATATGGTCCCC | 51317 |
rs547393826 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45967847 | ATCAGCATGTGCCTA[C/T]AGACATGTATCTCTA | 51317 |
rs547405449 | snp | A/G | 1.64746e-05 | 0.00287002 | intron-variant | PHF21A | GRCh38.p7 | 11:45948844 | ACACACACACAAAGC[A/G]AAAGCAACAGCAGCA | 51317 |
rs547431480 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46118591 | AACTGTACACAAAAT[A/T]TCCTCTTTGCCATGA | 51317 |
rs547432742 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | PHF21A | GRCh38.p7 | 11:46011497 | ATTCAGTCTCAAAAA[A/C]AAAAAAGTGTTCAAT | 51317 |
rs547445596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46026354 | ATCCATGATGTAGAT[A/G]TCATGCACAAGGTAC | 51317 |
rs547453978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46101478 | TTAGGGAATAGGTAC[A/G]TGGGGTTATATTATT | 51317 |
rs547478685 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45940820 | CAGTGATGGAGTGAA[A/T]GAGACAAACTGGGCA | 51317 |
rs547512425 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46069108 | CTACATATATACAAC[A/C]TCTCGATCTTCAGAA | 51317 |
rs547514647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46059606 | CTTTTTAAATTTTGT[A/G]TAGAGGTGGGATGTT | 51317 |
rs547521934 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46035494 | AGAGAATATTCCCTT[C/G]AATAGGCAGGTGGAG | 51317 |
rs547522882 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46042802 | ACCTTCTTGCTATGT[C/G]CTCACAGCAAGAAGG | 51317 |
rs547525519 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45992973 | TAAAGAGCTGTAGAG[G/T]AGAGGTCAGAAAACT | 51317 |
rs547551114 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46068682 | GGAAAAAAAAAATAC[A/G]GTAGATTCCAGTCAG | 51317 |
rs547558292 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46050106 | CACTAGGGATTGCCA[A/C]TGAAAGGAAATGCTT | 51317 |
rs547566929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46033852 | TTCTGTTCTATTTCT[A/G]TTGGACAGTGCTGCT | 51317 |
rs547652435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46042394 | GTGATAGTGCAACTC[C/T]GGAAAGTTCATCACC | 51317 |
rs547665139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45948155 | GATGTATTACTGACA[C/T]CAAAGAAAAATTTCA | 51317 |
rs547683826 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46066802 | CACTTCTTAGAGGCA[A/G]TCACTGTGAATGGTT | 51317 |
rs547688133 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46025531 | ACAAAAGAAAAATTC[C/T]TTTACCTGAGAAGAA | 51317 |
rs547718078 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PHF21A | GRCh38.p7 | 11:46065634 | ATACAATTATAACAT[C/G]TATATTACAGTTGAG | 51317 |
rs547734691 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46049625 | TCCCACCTGTCACAG[A/C]ACTCTCCTTGCTGGT | 51317 |
rs547749552 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45957711 | AAATCAATAACCTAA[C/T]TTTACACCTTAAGAA | 51317 |
rs547763105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46109397 | TAAGGTACAAAAACC[A/G]TTCACAACTTGTCAA | 51317 |
rs547775789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46016653 | TGACATAATCTATTT[C/T]ACACTGCAATTTGTA | 51317 |
rs547779174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46057629 | AGCTGAAATAAGTAA[A/G]ATCACCTAAAACCCT | 51317 |
rs547787967 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46001288 | TTCTGTGACCACCAG[G/T]GGGGCTGGAAATGGG | 51317 |
rs547789464 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46117603 | TTTCAACACACTATA[A/C]CCCTTTCCAAAATCT | 51317 |
rs547789832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46010155 | AAGACAAAAACTAAA[A/G]CTCTCTCCTGATATA | 51317 |
rs547814742 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45966541 | TTGGGTTCAAATCCT[A/C]GTTCTACCACTCACT | 51317 |
rs547843629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45983556 | CTCTGTCACTTAAAT[A/G]TAGATGACTGCACTT | 51317 |
rs547888318 | in-del | -/CG | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46072810 | TCAGGCTGGGGAAAC[-/CG]AAGCTGCAACCACGA | 51317 |
rs547888945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46041606 | ATTCCAAAGGTACAG[A/G]TCCTACCCAATTTGT | 51317 |
rs547901680 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46017594 | GGGGAAAAAAAAAAA[A/C]CACCTCCCTCATCTC | 51317 |
rs547908724 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45992367 | GAAACCCCGTCTATA[A/C]TAAAAATACAAAAAA | 51317 |
rs547914535 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46035266 | ATTTCCTGAAAAAAA[C/T]CCATCTTTCTCTACT | 51317 |
rs547959174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46015617 | TATAAAAATACTTTT[C/T]TTATCCTTATGTTTT | 51317 |
rs547972425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45965801 | GAGGTCCAAACCTCA[C/T]CCTAGAACATAGCTT | 51317 |
rs547997163 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45971574 | TAGTTTTCAAGAGTT[A/C]TCATATTGGTGTCAC | 51317 |
rs548020954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45967147 | GCTGAGGCTGGTGGA[C/T]CACTTGAGGCCAGGA | 51317 |
rs548041817 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45967790 | AACGACCCTGTGGTG[A/G]GTGCTACTGACTTAA | 51317 |
rs548055137 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45932903 | GCTTTTCTATTCCTT[A/T]TTTTAGTTTTTGTTA | 51317 |
rs548077443 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46104581 | TACTCTTTCTCACCA[C/T]GCATTTCAAGGGAGA | 51317 |
rs548107887 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45983505 | CTGTGAAAAAAAAAA[A/T]TTTTTAAATCAAGAT | 51317 |
rs548109052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45956647 | ATGTTTACTGTAATC[C/T]CCAAGGTAACCACTA | 51317 |
rs548118663 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PHF21A | GRCh38.p7 | 11:45940043 | CTATGATGTAATCCC[C/T]CCACCACCACTAGTG | 51317 |
rs548128212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46101423 | CTGTTATGTTTTACA[C/T]ACTATAAATAAAGAT | 51317 |
rs548130483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46116923 | AGTGAGCCGAGATCA[C/T]GCCGTTGCACTCCAG | 51317 |
rs548143525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46085866 | TTCTCATTAGGCATA[A/G]AACATCAGCAGAAAT | 51317 |
rs548154896 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46117437 | TACCACTGATACAAC[G/T]TGACTTACAGTTCAA | 51317 |
rs548231741 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46084971 | AGGCGTGAGCCACTG[C/T]GCTGAGCCAAAATCA | 51317 |
rs548249174 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PHF21A | GRCh38.p7 | 11:45991366 | GATATTACTTGCCAG[A/G]TAGAACAATGAGGCT | 51317 |
rs548249525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46109219 | TACCTATGTGATCCG[A/G]GGGAAACCTCTACTT | 51317 |
rs548263294 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46067729 | TAACATTCAAAAACA[C/T]TTGCTGCTCATCTAC | 51317 |
rs548270304 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46071050 | TTTTAGACTAAGTGC[A/G]GTAGATGAATTACTG | 51317 |
rs548273507 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45948813 | CTATAATGATGGGAG[G/T]AGGGAAGGAGAAGAA | 51317 |
rs548286230 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45958664 | TTCATGCCTATAATC[A/C]CAACACTTTGGGAAG | 51317 |
rs548315632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46117509 | ATGTATTTATAAAGC[C/T]GAGTGCCTAAAAATT | 51317 |
rs548338163 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46075680 | AATAGGAGGGAAGAA[A/T]ATAAAGCAGTTGTTC | 51317 |
rs548344689 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45993634 | ACTGAATGCAGAGTA[C/T]ACTAGTATGGGGAGC | 51317 |
rs548396730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46081707 | CAGAATGCGGCAATA[C/T]TTCTTGAGGATATAC | 51317 |
rs548400386 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46009220 | CTCAGGTAATCTGCC[C/G]GCCTCGGTCTCCCAA | 51317 |
rs548408882 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | PHF21A | GRCh38.p7 | 11:46031599 | GTTGATAATAAACAT[A/G]CATAATTAGGCAGTT | 51317 |
rs548422828 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46066541 | TGTTTCTAAAAAAAT[A/C]AAAATAAATTAGCCA | 51317 |
rs548427802 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46073717 | ATTTCAGAGCACATT[C/G]CTGTATCATTAAAAT | 51317 |
rs548449065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46032487 | ACCAAATGTTTTTTT[C/T]AATTCTCCACTATTA | 51317 |
rs548451751 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:45955629 | ATGGTTCAAATTTCT[C/G]TCTCTCATGCAAGAA | 51317 |
rs548466764 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:46084277 | CAGCCTCTGTTTAAA[A/G]TAACAAACTCCTCTT | 51317 |
rs548484554 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46014265 | TGAGAACATATAATA[C/T]TCAGTTTTCTGTTTC | 51317 |
rs548486557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46042291 | AACCAAACTTTAAGA[C/T]TGCTGGACAGGTATT | 51317 |
rs548503938 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46073197 | GCCAGGCGTGGTGGC[A/G]GGCGCCTGTAGTCCC | 51317 |
rs548520492 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46118562 | TACAGAAATTTTTTT[A/G]TAAACATTAGCATAA | 51317 |
rs548522089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45944314 | CCTTGTTCCCCTAAA[A/G]TAAGTGTGTATGGTA | 51317 |
rs548557673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46008621 | GGTGGAAATGTGACT[C/T]GGTTTTGTGTATGAA | 51317 |
rs548645527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45973554 | GTAAACGCGGAACAC[C/T]GATATTTATTTTGGG | 51317 |
rs548654445 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45959819 | AGGGTCTAGTATCCA[G/T]ATTATATAAAGAACT | 51317 |
rs548657239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45944894 | GCCTCAGCCTCCAGA[A/G]TAACTGGGATTACAG | 51317 |
rs548661529 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45939245 | TAGAGGACAACCTAC[A/G]TATCATAAATCTTAC | 51317 |
rs548675416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46104336 | TGCCTAGTCTACTAC[C/T]GACTTGATTCTAAGA | 51317 |
rs548682448 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45972607 | ACATGGCGAAAGCCC[A/G]TCTCTACTAAGAATA | 51317 |
rs548695537 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:46048654 | ATACACCTGTAATCC[C/T]AGCTACTCGGGAGGC | 51317 |
rs548720099 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46122411 | ACCCTTGAACCACTT[C/T]ATTAGCAGTACTTAG | 51317 |
rs548742028 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46054012 | TTTGCCCCCACTTCG[C/T]CACAAGCTTTTTCAC | 51317 |
rs548757591 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46022917 | CACCACACTTGGGTA[A/C]TTTTTGTATTTTTAG | 51317 |
rs548808026 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PHF21A | GRCh38.p7 | 11:46030913 | GGAAGTGGAGGAGAC[C/T]GACCAGAGAAATTGC | 51317 |
rs548816661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45996446 | ATGCTGGTTAAGAAC[C/T]AGCACTAAGTCTGTC | 51317 |
rs548838114 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46104292 | ATGGACTGACCAGCT[C/G]ATGAGTATTTAAGAC | 51317 |
rs548845766 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45951574 | CTTTGTGGTTGCCAA[A/C]TAACTACATTCCTAA | 51317 |
rs548859825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46070480 | GTACTACAGGTGCCC[A/G]CCACCACACCCAGCT | 51317 |
rs548877051 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46100581 | GGTCCTGTTAAGTAA[A/G]TATACTCCTTGCACT | 51317 |
rs548908728 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45968910 | CACTCCAGCCTGTGC[A/G]ATGGGAGCGAAACTC | 51317 |
rs548925119 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46014829 | ACTAAAAATACAAAA[A/C]ATTAGCTGGGCGTAG | 51317 |
rs548932537 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PHF21A | GRCh38.p7 | 11:46062247 | GAATTATATGCCCTT[C/T]GGTTGTGGGACATTT | 51317 |
rs548937827 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45929921 | CCTGCCAGGGGTGCC[C/T]GGCAGAGGGACAGGG | 51317 |
rs548977894 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46087764 | AATATTTTGAAAAAA[-/T]TTTTTTCCTGAGATA | 51317 |
rs548996790 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46005200 | AAAACTTTTTGAGCA[A/C]TGACGTGATGCCACA | 51317 |
rs549006005 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46000924 | AACCTCCGTCTCAAA[A/T]AAATAAATAAATAAA | 51317 |
rs549009580 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46043159 | CCTTTAGAGGTAAGA[A/T]ATTCAATCAATGTAA | 51317 |
rs549023069 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46117569 | CCGAGGGGAAAAAAC[C/T]ACAAGAAGTCTAAAA | 51317 |
rs549034699 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45997588 | AACATTTTTCATTTC[C/T]CAATGAATAGAATTT | 51317 |
rs549045069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46053909 | ATTACAACCCCTCCA[A/G]TGAGATTCCAGGCTT | 51317 |
rs549070169 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PHF21A | GRCh38.p7 | 11:46113959 | TTCTAATATTGCCCA[A/C]CAGGAAATAATTTTT | 51317 |
rs549078716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46044560 | CTTCTCTTACTCTTT[C/T]GGGCAACCCAGATTA | 51317 |
rs549111508 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46006128 | TTTACGATTAAAGAA[C/T]CAGATTAACTGACAA | 51317 |
rs549158300 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46019210 | AAAAGAAGAAACTGC[C/T]TTTTAATTCTTTCTA | 51317 |
rs549172076 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46096405 | TCTAATTCCTCTCCT[C/T]CCAATCTCTATTGAA | 51317 |
rs549184318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46087716 | AGAGAAGGGGTCTCA[C/T]ATGTTGCCCAGGCTG | 51317 |
rs549197623 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46018436 | TCTGGTGTATTTGGC[C/T]AGTTGGGAAAAATCT | 51317 |
rs549202040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46010386 | ACAATCTTGTGAAGA[C/T]ACTTTACAGAAGAAT | 51317 |
rs549240134 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46087577 | AGAAAGATCTCTTTC[C/T]GGATAGTAATTTTAA | 51317 |
rs549263759 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46119697 | TACCAACCCCTCCCC[G/T]ACCAGGGCCACCTTG | 51317 |
rs549275517 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46039209 | AGAATACTAATGAAA[C/T]GTTTAAAAAGTTATC | 51317 |
rs549278829 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46084066 | GACAAAATTGTCTTA[A/C]AGATTATTAAAAACT | 51317 |
rs549300766 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45970020 | TCTACAAGCTTTCAT[C/T]GTAAGTTAATCATCT | 51317 |
rs549313358 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46035254 | TGTTCTTATACCATT[G/T]CCTGAAAAAAATCCA | 51317 |
rs549316344 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:46121170 | CCTCTCCTCTCCTCT[C/G]TCTCTCACTCACTCT | 51317 |
rs549333413 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | PHF21A | GRCh38.p7 | 11:45934720 | GAAGTGAGACGACAG[A/G]CCAGCAGCATTTAGG | 51317 |
rs549364408 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46051919 | TAAAATATCCAAAAA[C/T]AGCTTTTCTATCAAG | 51317 |
rs549383613 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45985569 | TAGAATTCTAACAGA[C/G]GAAGACAGGGAGGAA | 51317 |
rs549383925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46103155 | GGACAAACTGATTTT[C/T]AAAATTGTATAATTC | 51317 |
rs549436117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45995200 | TATTTGTTGTCTGAT[A/G]GGATACAGTGGAACG | 51317 |
rs549465749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45977479 | TACTTGAACAGGATG[C/T]TTCCATGGGTTAAGA | 51317 |
rs549467773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45951544 | TTTCTAAACTGTATG[C/T]TGAAATGACATACAC | 51317 |
rs549492104 | in-del | -/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45942466 | CCTTTGGCAATACTT[-/C]CAACTGAGAAAAAGT | 51317 |
rs549501868 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46122366 | CGCCCGCTCCCTCCC[C/T]TCGCCACCCCGCCCC | 51317 |
rs549507637 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45941184 | GCTTACTGCAGCCTC[G/T]ACCTCCCAGGCTCAG | 51317 |
rs549528983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46069146 | ACTTGCAGCCAGTTA[C/T]TTCTGAGCCTTTCCT | 51317 |
rs549540812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46085991 | CACATTTGCAAAGGA[C/T]AGGAAAAATTTACTG | 51317 |
rs549545622 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:45986327 | ATATGTATGACTATA[A/G]AAGACTAATATTGAT | 51317 |
rs549551802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45949952 | TCAGAAAAAGAAGAG[C/T]TCCCCTAAATGAACA | 51317 |
rs549560542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46059064 | GATTAAGCTAGTTGG[A/G]GTTAGATTCTACTAT | 51317 |
rs549607056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46068462 | CTCCTAAAAAGCATT[C/T]GTTATTCACACTGCC | 51317 |
rs549613160 | snp | C/T | 3.29527e-05 | 0.00405898 | intron-variant | PHF21A | GRCh38.p7 | 11:45949353 | GCACTGAACAGCTCA[C/T]AAATAAAACTGGAAC | 51317 |
rs549615036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45959773 | CAAACTACGGAACAG[A/G]AGAAAATATTTGCAA | 51317 |
rs549618844 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46004220 | TGCATACTGGTAAGA[A/T]ATTTCATCCAATGTT | 51317 |
rs549620490 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46077488 | ATTAAAGTTTTCAAA[A/T]GCTTAATGTAGCAGG | 51317 |
rs549668435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46102107 | GTGATCCACCCGCCT[C/T]GGCCTCCCAAAGTGC | 51317 |
rs549702146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46086792 | GTTCAATTCAATTCA[C/T]ATAAACTCTGGAAAT | 51317 |
rs549708273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45968104 | GGATACTCCATGTAA[A/G]GTGCCTAGCATAGTA | 51317 |
rs549728655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46050934 | TGTATGCTACACAGA[C/T]TTTTTTCTAGTAAAT | 51317 |
rs549814207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46005048 | ACATGCATGTATACA[C/T]CCAACTAATACAGCA | 51317 |
rs549818405 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:45956763 | ACAGGAAATGAAGAA[C/T]AAAAAACGTAAGATA | 51317 |
rs549838274 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46061504 | TTGTACAACATTTTG[C/G]TATTCCTGGAACTTA | 51317 |
rs549851001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46012272 | CTATTACTGACCATG[C/T]TCTTCTTGGGCCTCT | 51317 |
rs549853316 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45972259 | AGCTGTACTTTTCTA[C/G]ACTTTTTACTAGAAT | 51317 |
rs549894060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46052200 | CAAATAAAAAAAACT[C/T]TCCCTCTTCAATGGA | 51317 |
rs549919634 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46078161 | TTCTCACGGAAGTAG[A/G]ATCATTCAAAAGGAA | 51317 |
rs549938359 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45941134 | GACCGGGTCTGGCTC[C/T]GTCACCCAGGCTGGA | 51317 |
rs549946442 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46110046 | ATTTTTTGGTTCTAA[C/G]TCATTATTTAAAATT | 51317 |
rs549961729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46026547 | GCTACCTCTTCTCTA[C/T]CCTGTTCGCCCCTCA | 51317 |
rs549962490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45985239 | CCAATATTCATCAAC[A/G]CTGAGGATGCAGGAA | 51317 |
rs549970742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46093979 | AAATTAAGAACTTCT[A/G]CTCATCAAAAAAACA | 51317 |
rs549993491 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46042807 | CTTGCTATGTCCTCA[C/T]AGCAAGAAGGTGCTA | 51317 |
rs550009694 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46102063 | GGGTTTCATCATGTT[G/T]GCCAGGATGGTCTCA | 51317 |
rs550033487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45968848 | AGGAAGGAGAATCGC[C/T]TGAACCTGGTGGGTG | 51317 |
rs550048688 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45933890 | ACTTTCCAGAAATCC[A/G]GCTTTGCTTTTCTAG | 51317 |
rs550049230 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46116792 | ACATGGTGATACCCC[A/G]TCTCTACTCAAAATA | 51317 |
rs550051693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46058850 | GAAGATACAAACATG[A/G]GAACTTCGCAGGGAC | 51317 |
rs550085879 | in-del | -/CACACG | | | intron-variant | PHF21A | GRCh38.p7 | 11:46114100 | CTACACACACACACA[-/CACACG]CACACATCCCCACAC | 51317 |
rs550092843 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45946597 | AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTCAT | 51317 |
rs550095208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45977388 | GTGATCCACCCACCT[C/T]GGCCTCCCAAAGTGT | 51317 |
rs550119710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45941762 | GGTAGGTAAGTTGAA[A/G]AACAGCTGGCCCATG | 51317 |
rs550120730 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46075645 | CTGTCTGTGGAGAAG[A/C]CAAGATGGGGACGCA | 51317 |
rs550121734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46042464 | GACACGTTATAAGAC[C/T]GGACTAAAATCACTG | 51317 |
rs550122245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46027132 | CTCCCAGATTATAAA[C/T]AGGCTGCCAATCCAA | 51317 |
rs550125452 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46082326 | TCGTCAAATGTATGT[C/T]CTGGCTTTGGTCTCA | 51317 |
rs550129062 | in-del | -/ATCTATCT | 0.121675 | 0.214552 | intron-variant | PHF21A | GRCh38.p7 | 11:46015903 | TACAGTCATCTATCT[-/ATCTATCT]ATCTATCTATCTATC | 51317 |
rs550129842 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46002669 | TTTAAGGGATATAAT[A/G]AAGAACTTTGGACTC | 51317 |
rs550133266 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930480 | TTACCCCAAAGGGCC[C/T]GATAAGGAAGGAAGA | 51317 |
rs550136140 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46101679 | GCTTTGTTGCCCAGG[A/C]TGGAGTGCAGTGGCA | 51317 |
rs550174941 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46110511 | GTAATCACATGGGTA[C/G]ATATAATGATAAAAA | 51317 |
rs550179268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45993104 | TTTAACTGGTTCTCA[C/T]TTCTGAGTACTCTGA | 51317 |
rs550189344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46111204 | CCAGGCGTGGTGGCT[C/T]ACGCCTGTAATCCCA | 51317 |
rs550200592 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46092021 | GTTTGAAGTATAGCT[A/T]CGTGAAATTAGACAA | 51317 |
rs550210497 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46010362 | ACATTATGTTACTTA[A/T]ACCTCGCAACAATCT | 51317 |
rs550236602 | in-del | -/AATTTGTAGAGAT | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:46078239 | TAGACCTGAGTTCTC[-/AATTTGTAGAGAT]AAGTGTTATTTTTTT | 51317 |
rs550238399 | in-del | -/AAAAAGAAAC | | | intron-variant | PHF21A | GRCh38.p7 | 11:46022467 | CTCTTAAAAAAAAAG[-/AAAAAGAAAC]AAAAAGACAGGGTCT | 51317 |
rs550272279 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930914 | TCACAGGCCCCCCCC[A/C]CTCCCCGCCCAGGTC | 51317 |
rs550278168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46038679 | TGAGGACTCTCTGCA[A/G]AGTCCCAAGGCAGCA | 51317 |
rs550281104 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45984587 | CAACAGAAAATCAGG[G/T]TCGTTTTTCCACCGT | 51317 |
rs550281826 | snp | A/C/G | 0.000181319 | 0.00951998 | synonymous-codon, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45938211 | AATTGTTTTCAGAGG[A/C/G]GGGTCTAAGCAGTCC | 51317 |
rs550287925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45999089 | GCCTCAGCCTCCCAA[A/G]GTGCTGGGATTACAG | 51317 |
rs550291668 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46098219 | TGTACATAAATAAAT[C/G]GAAGTAATAAAAATC | 51317 |
rs550340067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45993900 | TATCTGAGATGAATT[C/T]CCTAGAAACTGCTCT | 51317 |
rs550341338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46009554 | CACAGTTCTAAGCAC[A/G]CTATGTATTACATAA | 51317 |
rs550358742 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45958520 | AGTCCCAGCTACTTG[G/T]GAAGCTGAGGCGGGA | 51317 |
rs550378146 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46016734 | AGACTAGGTCTTGCT[G/T]ATTTTATAGCCCACT | 51317 |
rs550396867 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46021678 | TCTCAAGTCTCTGAG[A/C]CTATAGGCACACACC | 51317 |
rs550421924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45957869 | AAAAGAATAACAAAA[C/T]CGACAAACCTCTGGC | 51317 |
rs550463406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45945253 | GAATTCTGAGCTTTG[C/T]TGAGGTTCATTTAAA | 51317 |
rs550464026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46001874 | AACCCAGATGGGCCA[C/T]AATACAAGATACTTA | 51317 |
rs550473142 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46095723 | ATCTGAAACCCTTGC[A/G]ATATGAAGAATCTGT | 51317 |
rs550490276 | in-del | -/AAT | | | intron-variant | PHF21A | GRCh38.p7 | 11:46028433 | TACTTTCATAATTAG[-/AAT]AATAATTATACAATC | 51317 |
rs550520708 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46062432 | ATTGAGAAACAACTC[C/T]AATTTTGTTTTCCAA | 51317 |
rs550558421 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46103062 | CACAGGAGCACCACC[A/G]GCTGGACAGGGTCCT | 51317 |
rs550588941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45937529 | CTTGTCACCCAGGCT[A/G]GAGTGCAGTGGTGTG | 51317 |
rs550609853 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46090099 | ATTATCCCAACCACA[C/T]CCAACAAAAGGAAAA | 51317 |
rs550643463 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45949363 | GCTCATAAATAAAAC[C/T]GGAACATGAGGGAAG | 51317 |
rs550662994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45981694 | AGAAAAAGAAGTGAA[C/T]GAAGAGCTTTAAATA | 51317 |
rs550704900 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45941328 | TGGTAAAAACTTTCA[A/G]TTCTGAATTACAGAA | 51317 |
rs550705827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45970304 | ATGGCTTTATTCCTA[C/T]AGAAAATTTTCTAAC | 51317 |
rs550725493 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45980481 | AGTACTCAGAACTGT[A/G]ATTGGCACATTGTTG | 51317 |
rs550739688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45990450 | TTTTTAGTAGAGACA[C/T]GGTTTCGCCATGTTG | 51317 |
rs550742925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45996201 | CTCCTGGCTCGGCCT[C/T]CCAAAGTGAGCCACC | 51317 |
rs550746594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46028494 | CCCTCCTGAAACTCT[A/G]AGACTTCCTGATTCT | 51317 |
rs550750805 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46071490 | CACATTATTAAAGTG[A/T]AAGTTACTTCATCAA | 51317 |
rs550752377 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45954060 | GGAGTGCAATGGCAT[C/G]ATCTCAGTTCACTGC | 51317 |
rs550775759 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45951247 | TCAATTGTAAAAGAC[A/C]TACTCCTGTAGAGTT | 51317 |
rs550784663 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45990394 | TCCCCAAGGAGCTGG[C/G]ACTACACGAATGCAC | 51317 |
rs550787812 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46112835 | CAATGAATGATGCCA[C/T]AATTATAAAGAGACC | 51317 |
rs550812408 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45983088 | AAGCAGGAGCAAGGG[A/G]TGCGGGCTAGAGTAC | 51317 |
rs550815548 | snp | C/T | 0.000537463 | 0.0163842 | intron-variant | PHF21A | GRCh38.p7 | 11:45953518 | CTGCCTTTGGAAACA[C/T]AGGCCTACCTGAGGG | 51317 |
rs550821516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45998713 | GACGGGGTTTCTCCA[C/T]GTTGGTCAGGCTGGT | 51317 |
rs550827617 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46060733 | GACCTTTGTCAGATG[C/T]ACAGTTTGCAAACAT | 51317 |
rs550868343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46106323 | CAAAAGGGTGGGGGG[A/G]AACCATCAGCTTAAA | 51317 |
rs550880721 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46063172 | GGTGTTCAAAATGAA[C/T]TGAATTCGCCGGGGG | 51317 |
rs550883388 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46104088 | TAAGAAAACATCAGG[C/T]ACCAAATGAGAGGAA | 51317 |
rs550906363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45987761 | TAAATTAAGCTCCAA[C/T]AGAGCAAAACGTCTG | 51317 |
rs550915457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46029275 | ATACTTGTTGAATTT[C/T]TCCTCACATAATAGG | 51317 |
rs550961345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45978349 | AAAACAGAGATGGTA[A/G]TAATAATAACTTCCT | 51317 |
rs550973875 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46063117 | TGGGGAGAGGAATAG[A/G]GACGAAGAGAATAAA | 51317 |
rs550974029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46054153 | TAAAATACACTAGTA[A/G]AAGTTGTATTCCTCT | 51317 |
rs550979210 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46051228 | TACTAGATCTAATCA[C/T]TGCTGCTTTAAAGAG | 51317 |
rs551008579 | snp | G/T | | | upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46122258 | AGCGAGGAGAAGTGA[G/T]GGGGAAGCACTGCAA | 51317 |
rs551022875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45941471 | TAAACCCCACTGTTC[A/G]GTCTTGAGAGAATGA | 51317 |
rs551030941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46097710 | AACCATCCTAATTCC[C/T]AATTCTTCCTTTGTT | 51317 |
rs551050023 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46080351 | TTTTGTAGAGACAGG[G/T]TCTTGTTATGTTGCC | 51317 |
rs551053607 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45937388 | TAATATGTTTGCCTT[C/T]TAAGTCTATAAAATA | 51317 |
rs551078832 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45962446 | AGAAAACAAGGATAG[G/T]TGAAAGATACGAAGT | 51317 |
rs551084253 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45964026 | AACATGGAGAAACCC[C/T]GTCTCTACTAAAAAT | 51317 |
rs551097868 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45971510 | CTGTAGAACAACATT[A/T]CTTTTGTGTACATAC | 51317 |
rs551136089 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46079547 | CCCACACAAAACCGG[C/T]CTGTTCATACACAGA | 51317 |
rs551172943 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | PHF21A | GRCh38.p7 | 11:46007309 | TCCATCTACCTTTTT[A/T]CTTCTTCTTCTTTTT | 51317 |
rs551221238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46097040 | CCAACCATGTGCCTC[C/T]ACCTTCAAAATATAT | 51317 |
rs551228687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45988516 | AAGTACATTCTTAAT[A/G]TCACACTCTTGATGC | 51317 |
rs551236436 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46026727 | AAAAAACCTGAGACA[C/T]GTTGGCTTGGCAATC | 51317 |
rs551247400 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45952416 | CTGGCTAATTTTGTT[G/T]ATTTTTTGCAGAAAC | 51317 |
rs551256195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46104827 | GTATGCAGCACGTAT[A/G]TGATACATCTTTATT | 51317 |
rs551281485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46045271 | TACCATGTGTGTTTA[C/T]TTCTTTTTCCCTATG | 51317 |
rs551302293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46070586 | TCTGCCTACCTTGGC[C/T]TACCAAAATGCTGGG | 51317 |
rs551304116 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, missense | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45928917 | CCTCCGCCATCCCTG[C/T]TATTTAAATTATTTA | 51317 |
rs551310569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45961739 | TAAACATTAAATACC[C/T]GACTTCATTTCATCA | 51317 |
rs551315578 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46036883 | TATGTTTAAAAAAAA[A/T]TTTTTTTGTAGAGAT | 51317 |
rs551328223 | in-del | -/TCA | 0.00119737 | 0.0244387 | downstream-variant-500B | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45929162 | CAGTGCACAAGGGAG[-/TCA]GTGCTACATCCAGCT | 51317 |
rs551353552 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46052197 | AAACAAATAAAAAAA[A/T]CTTTCCCTCTTCAAT | 51317 |
rs551354775 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46048688 | GGCAGGAGAATCGCT[A/T]GAACCCGGGAGGCAG | 51317 |
rs551372635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45944989 | GCTGGTCTTGAACTC[C/T]TGACTTCAGATGATC | 51317 |
rs551373450 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45997880 | CCTAAAACTACCACT[A/T]CAATCAACTCGAGTC | 51317 |
rs551391523 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46044611 | ATTTTGCTTCTGCAA[C/T]GGTTATCCAAACTCT | 51317 |
rs551401759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46036144 | TGATGACTGAATTTC[A/G]GAGATGAGTGAAAGG | 51317 |
rs551415488 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45951056 | ACTGGGCCCTGAAGA[C/T]GGAACGTTAAGACTC | 51317 |
rs551534958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46004129 | TGAATAAAATCCTGT[C/T]TCCCCTTTTTCTTAT | 51317 |
rs551537540 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46078863 | TAAGCTATATGACAA[A/G]TATTAACTCAATATT | 51317 |
rs551542027 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46021191 | CAGCTTCCAGAGCAG[C/G]TGGAACTACAGGTGC | 51317 |
rs551550358 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46089860 | CTACACAGGTCATAC[C/T]TCCACTGCAACGTGC | 51317 |
rs551555278 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46080076 | CTAATGGAAAAATTT[C/G]TCACTCTCTTTTGGT | 51317 |
rs551562703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45962298 | GAGAACGTTGGATAC[A/G]GGTTTGGTAACTGTG | 51317 |
rs551568347 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46079492 | CTTTCAAATGTTGTC[A/G]ATGTCTAGAGTCCCA | 51317 |
rs551575121 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46017583 | TTGCCCTTAAGGGGG[-/A]AAAAAAAAAAACACC | 51317 |
rs551579880 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46120710 | GAACACCCCCCTTTC[C/T]CTCCTCCCTCCCACA | 51317 |
rs551591553 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46113637 | GATCGAGACCATCCT[A/G]GCCAACATGGTGAAA | 51317 |
rs551599345 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46122582 | TTGTGTAGCAGGGCA[A/G]TCACTGGGAATCGGC | 51317 |
rs551609107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45995973 | ATTTAGACACAGGGT[C/T]TCCACTGTCACCCAG | 51317 |
rs551609384 | snp | C/G | | | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46085675 | CACTACTCCTTAAAC[C/G]AATACAATAAGATTC | 51317 |
rs551614517 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46014706 | TATTCTGGGGCCGGG[C/T]GCGGTGGCTCACGCC | 51317 |
rs551624067 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46091958 | TTTTAACAGGTTATC[A/G]AACGGTGGAACATGC | 51317 |
rs551650500 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | PHF21A | GRCh38.p7 | 11:45953244 | ATCGCTCATCTTAAC[A/T]TTTCAAATTTGTAAC | 51317 |
rs551664970 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46006322 | GAGAAATCAGTAAAT[G/T]CTTAATCTTTCGGTT | 51317 |
rs551674537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46112017 | TTCTAACAGTGCAAA[C/T]ATTGTAAACAATAAA | 51317 |
rs551707889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46032418 | ACGAATACATTTCCA[C/T]GTGAAAATCAGTATC | 51317 |
rs551757168 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45987427 | GGCACTTTGGGAGGC[C/T]GAGGTGGGCGAATCA | 51317 |
rs551766309 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45987527 | TTAGCTGGGCATAGT[C/G]GTGGGCGCCTGTAAT | 51317 |
rs551777970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46096015 | CCACTGGCTTTACTG[C/T]TTTTTATCTACCCTT | 51317 |
rs551779709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46086942 | AGAAATAAGAATGAC[C/T]AACAAACATGAAAAA | 51317 |
rs551784403 | snp | C/T | 0.00358891 | 0.0422285 | intron-variant | PHF21A | GRCh38.p7 | 11:46029138 | ATTAAGGGCTTAACT[C/T]AAGAAGTCAACGATA | 51317 |
rs551784781 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46083124 | AGACGAGCTTGTTTT[G/T]GTAACAAATTTCTGC | 51317 |
rs551791257 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46044265 | TTTTGGCTTTATTGA[G/T]AATACATTATTAAAC | 51317 |
rs551793480 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46103164 | GATTTTCAAAATTGT[A/G]TAATTCTTTAACTCA | 51317 |
rs551803028 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:46031827 | ATCTGTAAGTACTCA[A/G]GGGTGACATTCACTC | 51317 |
rs551818516 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46038253 | TGCCTCAGCCTCCTG[A/G]GTAGCTGAGATTATA | 51317 |
rs551899898 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45978229 | TGTTTGAACCCAAGA[C/T]GGTGGAGGTTGCAGT | 51317 |
rs551919876 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46068192 | GTCACATGGAAGTAA[C/T]ACTGCCAAGATTTTC | 51317 |
rs551924021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46041375 | ATTTGGGCACTGTGC[A/G]TACTTCTTTCGAGCA | 51317 |
rs551932981 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45999897 | GGCATAGCAGTGGTG[A/G]ACAGGAAGGCTTGTC | 51317 |
rs551934889 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45967094 | CCTTTCCTGGCCGGG[A/C]ACAGTGGCTCACACC | 51317 |
rs551946065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46087785 | TCCTGAGATAGGGTC[C/T]TACTGTGTCACCCAG | 51317 |
rs551946926 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45982414 | AATGATGCAGAGTTT[A/G]AAGTCTTTGCAGAAA | 51317 |
rs551965381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45951316 | TTATCCTCGATATTA[C/T]CCTACTTTGGCCTGA | 51317 |
rs551971925 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45964070 | GGCATGGTGGCTGAC[A/G]CCTGTAATCCCAGCT | 51317 |
rs551979736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46111427 | GTGAGCTGATATTGC[A/G]CCACTGCACTCCATA | 51317 |
rs552000619 | in-del | -/A | 0.00953873 | 0.0683987 | intron-variant | PHF21A | GRCh38.p7 | 11:46055117 | CCATTTTGGACTTTT[-/A]AATTATGGCGAGAAC | 51317 |
rs552006794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45992161 | GATAAAGCCCATGGG[C/T]CACCAGTTTTCAACC | 51317 |
rs552015506 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46060418 | AAAAAAGGCAAGAAA[A/C]AAGTTGTAATCTTAG | 51317 |
rs552020299 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46104028 | TCTAGGCTCAACATA[C/G]GTAGCTTATGACAAT | 51317 |
rs552036717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46052946 | ATGCAGATACACATG[C/T]GCTACAAGATGAAGT | 51317 |
rs552057136 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46112756 | CAACTATCCCCATTT[A/T]AAAAAAAAAGGAACA | 51317 |
rs552058237 | in-del | -/G | 0.0103295 | 0.0711199 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46120359 | CCGAGGGACAGCCGA[-/G]GGGGGGGCGGGCGAG | 51317 |
rs552068707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46094925 | AATCATGAAATCCTT[C/T]AAACCTAAGGGATCC | 51317 |
rs552093272 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | PHF21A | GRCh38.p7 | 11:45934799 | TCAGCCGGGGACTTA[C/G]AGTCTTTTGCCCTTT | 51317 |
rs552120250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45947676 | TTAACCCCTGTCCTC[C/T]TAGCAGATACTGCCC | 51317 |
rs552214656 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46057212 | ACTTGTTTATTTTCC[A/G]TCTTGGAACTACATA | 51317 |
rs552248135 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45932598 | TTAATAGAAATCACT[C/G]TTTTTAGGAAACAAA | 51317 |
rs552272877 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46103660 | ATAGGAGCCATTATG[C/T]TACTTTAACTTAAAT | 51317 |
rs552273743 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46081388 | TAGCCACAGTCTTCA[A/G]TGAAAAAAGCTCTTG | 51317 |
rs552286140 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46077431 | TAGATGAGATACACA[A/G]AGCATGATTGCCTTT | 51317 |
rs552286874 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45966605 | TAATAGCCAGTTTTT[G/T]TTTTTTTGTTTGTTG | 51317 |
rs552323826 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46048625 | AAATACAAAAATTAG[A/C]CGGGCATGGTGGCAT | 51317 |
rs552328357 | snp | C/T | 0.00993419 | 0.0697739 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930470 | ACCAGCAGGCTTACC[C/T]CAAAGGGCCTGATAA | 51317 |
rs552333080 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46089305 | TAATATGTAGGTAGA[C/T]AAAATAATATCTTTA | 51317 |
rs552340176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46108086 | AAAATCCTACTTTTT[A/G]TTTTTTCTTTTTTAC | 51317 |
rs552344138 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46084070 | AAATTGTCTTAAAGA[G/T]TATTAAAAACTATAC | 51317 |
rs552359025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46008527 | ATGGGTCAAAGGTAG[A/G]AGACGGGAAAAGAGT | 51317 |
rs552372319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45939175 | GAGAGGTCTATAGTC[A/G]CCAAGGCCAAAATTA | 51317 |
rs552384473 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930352 | CAGCAGGGACAGAGA[A/G]GCAGGTGTTGCAGGG | 51317 |
rs552419348 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45982804 | AAAACCCAAAACAGA[C/T]CAAATCAGAAGAAGG | 51317 |
rs552436316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45938420 | GACAATCAGCTGCCT[C/T]GTTCCAGGAGTACTC | 51317 |
rs552441102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46039210 | GAATACTAATGAAAC[A/G]TTTAAAAAGTTATCT | 51317 |
rs552448470 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46100083 | CTTTTGAAACAAAAA[C/G]CACAAAGAAACAGGA | 51317 |
rs552463444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46091321 | ATTTTTTTCATAATA[C/T]ACACTCTCCTAATAA | 51317 |
rs552495059 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46090021 | CCTGGGGTCCAGGCT[A/G]TCTGAATATACACAT | 51317 |
rs552499264 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45972444 | CTGTATATTTGCACT[A/G]TCTGATTTGGCAGCC | 51317 |
rs552504141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45955567 | GCAATTAGCAGCAGT[A/G]CTTTTAAGGAAGGGC | 51317 |
rs552536467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46014709 | TCTGGGGCCGGGCGC[A/G]GTGGCTCACGCCTGT | 51317 |
rs552555750 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46073144 | CCATCCTGGCTAACA[C/T]GATGAAACCCGGTCT | 51317 |
rs552595322 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46022456 | GAGACCCTGTCTCTT[-/A]AAAAAAAAAGAAAAA | 51317 |
rs552610119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46073234 | TTGGGAGGCTGAAGT[A/G]GGAGAATGGCGTGAA | 51317 |
rs552621560 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45990128 | CTACACAAATATTTA[C/T]AGTCTTCACACCTGA | 51317 |
rs552630673 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46057980 | TGGAAATTCAAAACA[C/T]ACCTGTTTTCCTACT | 51317 |
rs552633228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46080670 | CTACTATTCTTTTTT[C/T]GTTTTTTGTTTTTTA | 51317 |
rs552643309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45981487 | GGGACCAAAGACCAA[C/T]AAATGGCTCATAAAG | 51317 |
rs552674201 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45978017 | TAAAAAACAGAGATG[G/T]TGGGCCGGTTGCGGT | 51317 |
rs552692968 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:46055854 | ATTATTTTACTTGGA[A/G]TTAAAAGGATATGGC | 51317 |
rs552714329 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46038343 | ATGTTGGCCAGGCTG[C/G]TTTTGAACTCCTGAC | 51317 |
rs552756501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46030195 | GGTTTAGAATCCCAG[C/T]CTCTGAAAAGAGCTT | 51317 |
rs552757996 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:45964981 | TTATTGGGCCGAAAC[G/T]AACATGGCGTTTTCT | 51317 |
rs552788069 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46081483 | AAAGGTTTTCTTCCA[C/G]ACACTGGAATTTAAA | 51317 |
rs552828216 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46038763 | CTCTTCCTTTTCTTA[A/T]AAAACCACTAGTTCC | 51317 |
rs552839815 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46081821 | GCCATACTCATTCAT[G/T]TATATATTGTCCGTG | 51317 |
rs552849806 | in-del | -/T | 0.0152052 | 0.0858568 | intron-variant | PHF21A | GRCh38.p7 | 11:45999860 | TATATAGAAACATCG[-/T]TAACTTTTCTCTTGA | 51317 |
rs552884122 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46013359 | CTTAGTAGCTATCTC[A/G]GTTATCAGATCAACT | 51317 |
rs552888564 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45929732 | GAGCCCTGCTTCCGT[G/T]TAGAGGAGGTATTTT | 51317 |
rs552889603 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46022314 | TTAAAAATTAGCCAG[C/G]TATGGTGGCTCACAC | 51317 |
rs552917972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46022133 | TAGAACAAAACCATG[C/T]ACTGTTTGTTTCTTT | 51317 |
rs552923537 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45960047 | GGTGTGGTAAGGATG[A/C]GGAGACAATGGAATG | 51317 |
rs552939373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46013586 | CACAGTCATGTGTTG[C/T]TTAATAACAGGGATA | 51317 |
rs552976244 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46012958 | TAGGGGAAAATTTAC[C/T]ATCAGTCCCCCTTAT | 51317 |
rs552982546 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930674 | CCAGTCATCACTGCC[A/G]CCAGGGCGCAGCGCC | 51317 |
rs552993395 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45972660 | GGCTCGTGCCTGTAA[G/T]CCCAGCACTTTGGGA | 51317 |
rs553047910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46113471 | AAAAAATATAATTTT[C/T]GAAATAGTTTTTTAA | 51317 |
rs553051882 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46006500 | ACGCTATATAAATAA[A/C]AAGGAGTCTAAAAGT | 51317 |
rs553059424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45963918 | ATAATTTATTTCTGG[A/G]CTGGGCGTGGTGGCT | 51317 |
rs553087731 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45929983 | CTCAACAGAAGCCAC[A/G]GGATCTGGAGAACCC | 51317 |
rs553108324 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45988784 | TAGTCCCAGCTACTC[A/G]GGAAGCTGAGGCATG | 51317 |
rs553113727 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46062066 | CATCTGATTCCCAAT[A/C]CCTGTTTGCAACTGT | 51317 |
rs553149528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45936743 | AAAGTTCCAAATATC[A/G]GCTTAGGAGAATCAA | 51317 |
rs553172851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45935857 | AGCTCCCATGAGTCC[C/T]ACAACCCAGTGCAGA | 51317 |
rs553193048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45996905 | TGACTACTAACTTAC[C/T]TTCTTTGGGCACAAA | 51317 |
rs553197446 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45978450 | TATTAAATGTTAACT[C/T]ATCTTTAGTGTTCTT | 51317 |
rs553199680 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46106448 | GTCCTGATAAGTTAA[C/T]GGCATCTGTTCCTTT | 51317 |
rs553202619 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45957394 | TTAGGCCACAAAACA[A/C]ATATTAATAAATTTA | 51317 |
rs553227807 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46053535 | GTTTTTCTTCATTAT[A/C]TATATAATTATATGT | 51317 |
rs553234405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46105409 | GATTAGATCACTGCA[C/T]GACTCAGGAAGTAGC | 51317 |
rs553246474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46019698 | AGCAATGAAATTTAG[C/T]CGTATTAGTCTCCGG | 51317 |
rs553279118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45969497 | AATAAGAAGTGTTAA[C/T]TGCATTCTTTCCCCA | 51317 |
rs553312183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46098330 | GCATATTAACTTCTA[C/T]ATGCTTGAAAAATGT | 51317 |
rs553334334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46027711 | TATGAGAAGACGCCT[A/G]TTGTTCCCATATGGA | 51317 |
rs553339967 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46010509 | GCCTGAATTTCTTTC[C/T]GCTTTACGACATTGT | 51317 |
rs553340996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45979591 | TATTTCCTTCTGCCA[A/G]TGATTACAAGTGATA | 51317 |
rs553343990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46001580 | TAACACTGAATTTTT[A/G]TATAAGAAAAGAACA | 51317 |
rs553348002 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45934463 | AACAGAGGGAGAAAG[A/G]GCATGCGGGCACCAA | 51317 |
rs553381014 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46009699 | AGAGCCAGAGCAGAC[G/T]TCCAACTTGGGCAGT | 51317 |
rs553385072 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45931700 | TCCTAGACTCTGGCC[A/G]TTCCCAGGGCCTGGA | 51317 |
rs553387238 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46099905 | CTTTAGGCCTAAAAA[C/T]TAAAAATGGTTCCAT | 51317 |
rs553396396 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45998262 | CCTTTGAGTCATCCA[C/T]AAATATCAATTTGCC | 51317 |
rs553402505 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:45980983 | GGCCTTGCTCAAATC[C/G]AAGAGAAATGTGTTT | 51317 |
rs553410385 | in-del | -/AGA | | | intron-variant | PHF21A | GRCh38.p7 | 11:46118715 | TAAACAAGTAAAGAC[-/AGA]AGAAGAGAATAAGAA | 51317 |
rs553426493 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46071549 | TCTTTGACCAGTTAG[G/T]TATAAGTACTGGCAG | 51317 |
rs553441582 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46015562 | ATTTTTAAACTTTTT[G/T]ACTCTTTGTAATAAC | 51317 |
rs553451545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46114252 | TCCAAACACAAGCTG[A/G]TAAGTTTGAGCTAGA | 51317 |
rs553485900 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46119146 | CAGCCCAAATTAATC[A/T]GATTCTAATATTCAA | 51317 |
rs553514936 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46088082 | TTTGAGGTCTTGGAC[A/C]TCTCATGCAGTCATC | 51317 |
rs553525401 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45997859 | CAATAGGTCCTCTTA[C/T]CAGAACCTAAAACTA | 51317 |
rs553540514 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46062635 | AGCAGCTTCCCTTAA[A/G]TATCTAGTGATTCTT | 51317 |
rs553546923 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45944608 | TATCCTGGCCCTCTT[C/G]CTTTTCTTTCAGGAT | 51317 |
rs553560689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45966189 | TTACCATCTATGTAC[C/T]GAAGACTCACACTTT | 51317 |
rs553562445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45975002 | TCTGCCTGCCAAATA[C/T]GAAGTATTGATTTAA | 51317 |
rs553586099 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46050315 | GGGACTAATACCACT[A/G]GGTCTTGTTGAAGAA | 51317 |
rs553589890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46078107 | AATCCAATTTAAATT[A/G]TGACTATACCAAAAA | 51317 |
rs553603825 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45946261 | GAAGGTGCTGGCTTA[C/T]GTAGAAAGACCTCAC | 51317 |
rs553615290 | in-del | -/C | 0.0138799 | 0.0821421 | intron-variant | PHF21A | GRCh38.p7 | 11:46028091 | AATCTCTGGGGACAA[-/C]TTTTTTTTTTTTTGA | 51317 |
rs553621651 | snp | C/T | | | upstream-variant-2KB | PHF21A, LOC105376661 | GRCh38.p7 | 11:46123391 | TTAAAAAATAAAATA[C/T]GGACTTTATGGTACA | 51317 |
rs553636315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46024673 | AGGTGTGGTGGCACA[C/T]GCCTATAATCCCAGT | 51317 |
rs553643924 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46037291 | GTGTCACAATCCTGT[A/T]CCCTCAGAATTCTAT | 51317 |
rs553645627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46020550 | TTTTCTGCTTCCCTT[A/G]CGTCTAACACCATCT | 51317 |
rs553664555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46070914 | CCTGTGACAGGGTAT[C/T]TCATGGGGAAAATCA | 51317 |
rs553664712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46084422 | GGCAAGAAATTTCCC[A/G]AAGAGATTTTTTTTC | 51317 |
rs553682086 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PHF21A | GRCh38.p7 | 11:46109997 | AAAAAAAAAAAAAAA[A/G]GTACTGGTCTATTGG | 51317 |
rs553698202 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45966746 | TGCCCCAGCCTCCTG[A/T]GTAGCTGGGGCTACA | 51317 |
rs553728497 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46072722 | TAGCTCCTCTGAGGA[A/C]GTGACATTTAAGCTA | 51317 |
rs553731369 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45958901 | CCAGTCTGGGTAACA[C/G]AGCAAGACCCTGCCT | 51317 |
rs553739429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46118179 | ATCCATCACTTATAC[C/T]TTCTAAAAATACAAT | 51317 |
rs553743203 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46100180 | AGACCTCAAAAAGAA[A/G]TTGTTTGCTTGATAT | 51317 |
rs553752102 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46079226 | CTCCCTATGGCTAAT[C/G]AGGTTTGGACCAAAA | 51317 |
rs553766926 | in-del | -/TCAT | | | intron-variant | PHF21A | GRCh38.p7 | 11:46107938 | AGGTGATGGGGATGA[-/TCAT]GGTCAGCCCACACTA | 51317 |
rs553767691 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45939427 | TACAGTGAAAGTTCA[A/T]ATGGGAAAATATTAA | 51317 |
rs553780072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46099595 | AACACAAAGGGAATG[A/G]TACTCTTTCACTTGA | 51317 |
rs553816656 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46092013 | ACAAATGCGTTTGAA[C/G]TATAGCTACGTGAAA | 51317 |
rs553824585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45974263 | ACCCCTACTCTGGTG[C/T]TTCTTCTTTCCCAAG | 51317 |
rs553834491 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45931971 | GAGGCTTGTGGGTGG[G/T]TGGAGTGGAGTAAAT | 51317 |
rs553857851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46049895 | AAAGCAACAGAATCA[A/G]GAGATTAAGTACTAA | 51317 |
rs553858682 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46068155 | GTGCTAATGAGCTTG[A/C]ATGCCTTGTAGGTCA | 51317 |
rs553860656 | in-del | -/T | 0.444554 | 0.156999 | intron-variant | PHF21A | GRCh38.p7 | 11:46110789 | CTACATATTAACAAT[-/T]TTTTTTTTTTTTTTG | 51317 |
rs553887964 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46016258 | TGCTAGTAGAACAAT[A/C]TTTCTCAAAAAGGGA | 51317 |
rs553899161 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PHF21A | GRCh38.p7 | 11:45933407 | TTTGATACACTGTCC[C/G]ACCCCCTGCTCCCTC | 51317 |
rs553923406 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:46101713 | CACAATCACAGCCTC[A/G]CAGCCTCGACCTACC | 51317 |
rs553946225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46059132 | GTATTCCTTATCTGA[C/T]TTTTTTTACTTCTAG | 51317 |
rs553969985 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46064960 | AAATAATCCACAGAG[C/G]CAGTAACAAGCACTA | 51317 |
rs553971624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46023917 | GCCAAGATCGTGCCA[C/T]TGCACTCCATCCTGG | 51317 |
rs554048459 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46032714 | TCTATCTCTTACAAG[A/T]ACACAGACTTGATAC | 51317 |
rs554055825 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46105616 | CTTCCCAAACACCAT[-/A]AAAAAAAACACAAAA | 51317 |
rs554060493 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46067147 | CATTTGTTTTCAAAT[G/T]TTCTTTTGTGGGGAT | 51317 |
rs554084303 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45957106 | GTTATAATCATATAT[A/G]TACCAGACAACAGAG | 51317 |
rs554085869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45946872 | TCAAGTTAACTATTC[C/T]TATCCCTTGCTTTTA | 51317 |
rs554097720 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46014991 | TCTCAAAAAAAAAAA[A/T]AAATAAAAATAAAAA | 51317 |
rs554104468 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46016883 | AATGATCAAAATTTG[G/T]ATCAGCAATTCTGGG | 51317 |
rs554143109 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45937534 | CACCCAGGCTGGAGT[A/G]CAGTGGTGTGACCTC | 51317 |
rs554145714 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45972988 | GAGGCTGAGGCAGGG[A/G]AATCACTTGAACCCG | 51317 |
rs554155744 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45931246 | TAGTGATGATGGTTT[C/T]CCAACTTCTTTCAGG | 51317 |
rs554174618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46040866 | TATAAATCTATTTCA[C/T]CCTTAGAACTACACT | 51317 |
rs554180139 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45962332 | AGGTGTGAACAGGTT[C/T]TTCCATGGCTACATA | 51317 |
rs554180718 | in-del | -/AT | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46034318 | AACCCTTTGTCACAC[-/AT]GTGTTAAAAATATCT | 51317 |
rs554192181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46015872 | CCTGAAGGACCTGCC[C/T]GAGGCTATTGCTGTT | 51317 |
rs554201694 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46117075 | CAGAAGCTTCTGTCC[A/C]TGTATTAATTAGTTA | 51317 |
rs554252702 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46063017 | CTTGATCGTGATGAC[A/G]GTTTCACACCATCAA | 51317 |
rs554267616 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46009618 | CTATATAGTATGCTA[C/T]TTTACAGATGGAGAA | 51317 |
rs554296683 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46105361 | AGCATGTGTGCCAGA[C/T]GTCTTTACAGGCACA | 51317 |
rs554296839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46116311 | ACACATACAGATATA[C/T]ATCTTTTTCACTGTG | 51317 |
rs554340755 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45996280 | TTAAAAACATAGGAT[C/G]TAGTACTCAAGGTAG | 51317 |
rs554363221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46058102 | AGGATCTCACTTAAA[C/T]CTGCAGAAAACAGAA | 51317 |
rs554395406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46007864 | TTTTCCATCTTACTC[C/T]TAAGTGGAATGTCAG | 51317 |
rs554397990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46117835 | ATCCTTATACTATCC[A/G]CAATCGCACATCTAC | 51317 |
rs554398347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46067051 | TCCATAATATGCATA[C/T]ATAGCTAATGTATTC | 51317 |
rs554400028 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46042675 | AACTGTATTATGAGG[C/T]GAGGTCTTTAAGAGG | 51317 |
rs554409610 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45990866 | ACATTTGTTACAATC[C/G]AACCTACACTGACAC | 51317 |
rs554453461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46091454 | TTAGGAAAAAATGTT[C/T]GCCTGTATGCCCCAC | 51317 |
rs554464432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46107584 | CGTGGATCTAAAGAA[A/G]CATAAAGCACCTTAG | 51317 |
rs554469033 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46000140 | CACAATAGTACCAGT[C/T]AAATTGTTAGTGAAG | 51317 |
rs554485079 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46056112 | CTCTGTTTCCTATCT[C/T]AAAGTAACAAAATAC | 51317 |
rs554508062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45999441 | CCAGTGAAATAGCAC[A/G]TAGTATATACTTCCA | 51317 |
rs554512135 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46065756 | TGTTTAAGCGCCACT[A/G]TGTGTGAAGCACTAG | 51317 |
rs554535203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45966079 | TCTGCCTCATCCTAA[A/G]TGTGAGTATTTCTTA | 51317 |
rs554539914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45989942 | GGCTGCAGTGAGCCA[C/T]GATCGTGCCACTGCA | 51317 |
rs554542336 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46117291 | GCAACCACAGTGGCA[C/T]GATATTTTCAGTGAT | 51317 |
rs554551545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46023889 | TGAACCCAGGAGGCG[A/G]AGGTTGCAGTGAGCC | 51317 |
rs554570837 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46065958 | CATGAGATGTTAGGG[A/C]GGGCACATCCAAGAG | 51317 |
rs554578381 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46116083 | GCTCATAAACACAGG[C/G]TTCCTAATTATCTAT | 51317 |
rs554596559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45974151 | GTTTGTCTAGTATAC[A/G]GGCACAAGACCTAGT | 51317 |
rs554597057 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45982176 | TGCCCAGGCTGGTCT[C/T]AAACTCCTGAGCTCA | 51317 |
rs554624131 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:45939734 | CACCATCAGAATAAA[A/G]CAGATCTACTTAAAA | 51317 |
rs554653983 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45990840 | ACTATCAACAAGCTA[A/C]ACATAGCAGAACATT | 51317 |
rs554658924 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45992282 | TCATGCTTGTAATCC[A/T]AGCACTTTGGGAGGC | 51317 |
rs554661493 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:45986853 | TCACTTGATTTTTAA[C/T]ATCTAATCATTTTAA | 51317 |
rs554673498 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46055905 | GCTAATTCAGAATCA[C/G]TTCCCATTTGGCAGG | 51317 |
rs554674878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46000442 | GCGATATGGGACTAA[A/G]GACAAGTACACAATT | 51317 |
rs554682083 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45949097 | CTCAAGGGTTTTATT[G/T]TATGTACTTGGCTCT | 51317 |
rs554683067 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46057154 | AAACTAAGAGCAGAA[C/G]AGTTTTTACTGGGTC | 51317 |
rs554702226 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46007733 | TTTAAATCAAAAAAC[A/G]ATGTGAAAGAAGTGA | 51317 |
rs554720300 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46023094 | GCTAAGGTCTCAGAC[C/G]TTGAGTGATATGTGG | 51317 |
rs554746351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45953910 | TTTAATTCCTAAGTA[C/T]AGAAATACGGTACAG | 51317 |
rs554746483 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46066515 | CCAGCCTGGGCAACA[A/G]AATGAGAACCTGTTT | 51317 |
rs554747761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45958016 | ACAAACTAGACAACA[C/T]AGATGCAATGGAAAA | 51317 |
rs554755163 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45931134 | GGTCAGAATGTACCC[C/G]ACACTGCTGAGGGCG | 51317 |
rs554764382 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46072643 | ACTATGAAGGAAAAG[A/T]ATGGTTCAATGTGAG | 51317 |
rs554786390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46082308 | GGCTTTTGTCCCACT[A/G]TTTCGTCAAATGTAT | 51317 |
rs554860276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46074149 | AGTTGTCAGATGCAA[C/T]TTTTTTTAATAAAAC | 51317 |
rs554877720 | snp | A/G | 6.87151e-05 | 0.00586113 | intron-variant | PHF21A | GRCh38.p7 | 11:45965273 | GCCATATGCCTCAAC[A/G]ACAAGGCTACTGCCC | 51317 |
rs554947121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46083484 | TACTTATCCTTCTCT[C/T]CGCTCCCATATCCCC | 51317 |
rs554954795 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45943372 | TTTGTAGAGACAGGG[G/T]TCTTGCCATGTTGTC | 51317 |
rs554971045 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46047761 | GTCACTTTTTCTTTG[G/T]GTCAATTTCATCTGC | 51317 |
rs554982954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45998902 | ATCTCAGCTCACTGC[A/G]GCCTCTGACTCTTGG | 51317 |
rs555001387 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | PHF21A | GRCh38.p7 | 11:46009135 | GTGCATCACCATGCC[C/T]AGCTAATTTTCTGTA | 51317 |
rs555009601 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46046685 | AATAATATTAAATGA[C/T]GATGGCAGCGGTGAA | 51317 |
rs555039000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46025237 | CAGAGTATGATTTCA[C/T]ACCACAGATACAAAG | 51317 |
rs555056435 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46099441 | CTTATTGTGTTCCAT[A/C]CTGCCTCACTTCTCA | 51317 |
rs555082497 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:45934405 | CACCTAAGGAACAGG[A/G]CGGGTGGAGTGGGTA | 51317 |
rs555095646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46040134 | ACTAGATGTGGTTTC[C/T]TCTGAACAACCTCTG | 51317 |
rs555105038 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45994631 | CAGCCTCACCAAGAG[G/T]GGTTATGTTTTAGGC | 51317 |
rs555109078 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46081104 | TCCTTTAGTAAAATG[C/T]ATAATCTTTGGTGTA | 51317 |
rs555162362 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46111234 | AGCACTTTGGGAGGC[C/T]GAGGTGGGCAGATCA | 51317 |
rs555178681 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46095139 | ATCAGAAATCCCAAA[C/G]TGTTTCTTCTGAAGA | 51317 |
rs555191300 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46026706 | TGGGCTTTTAAATCC[A/G]TAATTAAAAAACCTG | 51317 |
rs555199778 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45959092 | TTATCCCAAGAGTGG[A/G]AGGGTGGTTCAATGT | 51317 |
rs555218712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45942500 | GACAATCTTTGGCGC[C/T]AGCAAACAAGATTTC | 51317 |
rs555221892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45946356 | GATGTCAAAGCCCAG[C/T]GGGAGCCAGGGCCAG | 51317 |
rs555240873 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46065289 | AAAGTCTGTTGAAAG[C/G]CTTCTAATTAAAGTT | 51317 |
rs555251011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46013715 | GCTATATGGTAATAG[C/T]CTATTGCTTATGGGC | 51317 |
rs555266199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46120043 | GTGCAGGCAGACTCT[C/T]CGGAATAACAAGTTG | 51317 |
rs555295227 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PHF21A | GRCh38.p7 | 11:45934957 | TGCCACCAAGTACAA[C/G]GCACCACCTGGTATC | 51317 |
rs555316330 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46097193 | AAGGTATATTCTCTC[A/G]CAAGCCAGAGTAAGC | 51317 |
rs555319155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46013477 | GGGCCTCAGCTGACC[A/G]TGAGTAACTAAAGCC | 51317 |
rs555342433 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45995448 | TCACAGCATGTTTGT[G/T]TGACAGTTATACTGT | 51317 |
rs555350681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46052300 | AAGCAAATGAAGCCA[A/G]AAGAGGGAGAAAGTG | 51317 |
rs555398482 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46003220 | GAGTGCCACTAAAAA[A/C]AGTCCTAAAAACTTT | 51317 |
rs555403272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46068221 | TCATTCTCTGCATCC[C/T]CCATGGGCCTAGTAT | 51317 |
rs555403395 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46076581 | ACTCTAGAGACTGAT[C/T]TCAACCAAAAATAAA | 51317 |
rs555406257 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46043465 | AAAGCAAACAGAATG[C/G]CAAGTAAAGCCCATA | 51317 |
rs555407126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46059796 | CAGTGGCTCAATCTC[A/G]GCTCACTGCAACTTC | 51317 |
rs555419669 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46072426 | TATTTTGGACTATGA[C/T]GTGAAAGCTGCATGC | 51317 |
rs555429518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46025676 | GAAAATTCCTATATA[C/T]CTTTCACCCAAATTC | 51317 |
rs555508162 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46041797 | CTGAACTATCACACA[G/T]CTTTCTTCTCCCATG | 51317 |
rs555510165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46050282 | CAGTGTCCTTGCTCA[C/T]GGCAGGAGAAAGGCA | 51317 |
rs555521298 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46034262 | GGGAGGCTCATACTT[C/T]TCTTAGAGATTCATA | 51317 |
rs555525291 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46037001 | TAGGCAAAAGCCACT[A/G]CACCTGGCCAGTATT | 51317 |
rs555529639 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46093728 | GTTTGTTAAGTCAAT[A/G]AATTGACTAAACAGA | 51317 |
rs555544100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45960132 | TGGCAGTTCTTCAAA[C/T]AGTTGAGCAGAATTA | 51317 |
rs555561157 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46011314 | CCCAACATGGTAAAA[A/C]CCTGTCTCTACTAAA | 51317 |
rs555602022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45977467 | AACATAAAATGTTAC[C/T]TGAACAGGATGTTTC | 51317 |
rs555606964 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45967668 | GACAAATGTCTGATG[C/T]TATCTTGCTCACAAG | 51317 |
rs555620822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46042496 | ATGGTTTTTATAAAT[C/T]CTAGAAAACCGAAGA | 51317 |
rs555628581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46010579 | TTTGGCACCGGAGTA[C/T]GCTTTTTGGGTTCTC | 51317 |
rs555631576 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PHF21A | GRCh38.p7 | 11:45933239 | GAGATGCGCGACTCA[C/G]CAAGCAGGGAAGGAA | 51317 |
rs555647141 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46018677 | GCAAAAGATAATTTG[G/T]TAAACATGAACAAAA | 51317 |
rs555664938 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46121395 | CTTCATCCTCCTCCT[C/T]CTCTCAGCAGCAGCA | 51317 |
rs555683239 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46046694 | AAATGATGATGGCAG[C/T]GGTGAAGATCTAGGT | 51317 |
rs555698425 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45940353 | GGCGCCCACCACCAC[A/G]CCTGACTAACTTTTA | 51317 |
rs555754068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46093135 | TAATCAGTGATGAAG[C/T]CAGAAAGAAAATTTA | 51317 |
rs555754158 | snp | A/G | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46119960 | CCCGGCCCGCTCGGG[A/G]TCCCGGGGGCGCCCC | 51317 |
rs555774999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46110941 | CAGGCACCTGCCACC[A/G]CGCCCAGCTAATTTT | 51317 |
rs555809684 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45985896 | GTTGTCATGGAATTT[A/G]TATAGTACAAATAAA | 51317 |
rs555814749 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46033391 | CACCTCAGCCTCCCA[A/C]ACAGCTGGGACCACA | 51317 |
rs555839553 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46037802 | GCAACAGTATGAATC[-/T]TTTTTTTCCTCCAAA | 51317 |
rs555846027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46026701 | TCCTGTGGGCTTTTA[A/G]ATCCGTAATTAAAAA | 51317 |
rs555846484 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45994456 | CCTCCCTGCTTTCAG[A/T]GCTGCTACTAGGAAT | 51317 |
rs555847652 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46107822 | AAATATAATGCCAGA[A/T]AAAATGAACAGCACT | 51317 |
rs555941660 | in-del | -/CTCA | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:46080858 | TTTAAGAGATGAGGT[-/CTCA]CTATGTTATCCAGGC | 51317 |
rs555948787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45958243 | CTCTTAAATCATTCT[A/G]TGAGGCCAGCACTAC | 51317 |
rs555957808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46094475 | TCCACTAGACCTCAC[C/T]TTCTCTTAACCCGCT | 51317 |
rs555992072 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46110810 | TTTTTTTTTGAGACA[A/G]AGTCTTGCTCTGTCT | 51317 |
rs555996158 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45939170 | TACAGGAGAGGTCTA[C/T]AGTCGCCAAGGCCAA | 51317 |
rs555996778 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46102448 | TAATAAGGCATCAGT[C/G]GTATTCTGTATTTAC | 51317 |
rs556014014 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46012831 | GATACCCTAAGAGCT[C/G]ATGCTGGGATTTCTA | 51317 |
rs556029001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46109809 | CAACATGGTGAAACC[A/G]TCTCTACTGAAAATA | 51317 |
rs556033432 | snp | A/G | 4.94181e-05 | 0.00497057 | intron-variant | PHF21A | GRCh38.p7 | 11:45949390 | GAAGGGCCAGATGCT[A/G]GCCAGTAATACCTCT | 51317 |
rs556035965 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:45993178 | CATGTTATAAACATA[C/T]GACTATTTAATAATT | 51317 |
rs556043991 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:45944688 | GGCAGGCTCTTCCCC[C/G]AGATCCTCCCGAGGC | 51317 |
rs556049181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45975275 | ACCGTAATTGCACCA[C/T]TGCACTCCAGCCTAG | 51317 |
rs556084802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45959129 | ATCAATATAATATAC[C/T]ACATTAACAGAACCA | 51317 |
rs556087396 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45942106 | CTGCCACTACTGGGA[C/T]ACTGTAAAAGGAGAA | 51317 |
rs556099891 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46113419 | GTAGGAGAAGCACAG[-/A]AAAAAAATGCTGAAA | 51317 |
rs556116360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46097978 | CTTATTTAGAACCCA[C/T]AGATCTGTATTTAAG | 51317 |
rs556136651 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45938392 | ACATTCTAGATGCAT[A/G]TAAATGTTTTAGGAC | 51317 |
rs556145477 | in-del | -/ATTAC | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:46108047 | TCTATTAATTAAAAT[-/ATTAC]ATTACATGTATTATC | 51317 |
rs556157096 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46011218 | ATGAGGTTGGGCATG[C/G]TGGCTCACACCTGTA | 51317 |
rs556170360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45949550 | CTTAACTTCATTGTT[C/T]TATCTATTGGTTTTC | 51317 |
rs556172732 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PHF21A | GRCh38.p7 | 11:45933223 | CAGCGGGATAACCAC[A/G]GAGATGCGCGACTCA | 51317 |
rs556203507 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46085200 | TAACTGTACTATCCA[C/T]GAACTTATGATGTGG | 51317 |
rs556212649 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46050445 | CTTTTGAGAGGCCCA[C/T]GCAGGGAGGCAAATT | 51317 |
rs556226228 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46105153 | ATTTGGCCACAGTCA[A/G]AGCTAATACGTGGCA | 51317 |
rs556242304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46092980 | AGCTGGTATCAAACC[C/T]CTGGGCTCAAGCAAT | 51317 |
rs556258244 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46032919 | GTATGTATACATACA[G/T]GTACATATAATCTCT | 51317 |
rs556262714 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46101960 | ACTCCTGTGTTCAAG[C/T]GATTCTCCTGCCTCA | 51317 |
rs556278398 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45983676 | TAAAGGAGAGTTGCT[C/G]TGCATATTAGCTGGC | 51317 |
rs556291726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45934383 | CCTCAGTGGAGTGGG[C/T]GGCTACCACCTAAGG | 51317 |
rs556294749 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46041729 | ATACATAAAAGTTCA[C/T]AGTATAGTGATCCCT | 51317 |
rs556354849 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46057025 | GGTTATAGTAAGTGC[C/T]GAAAAAATTAAAATG | 51317 |
rs556355348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46017950 | CTAACTAGCTGTAGG[A/G]GTTAAAAAATGTGTC | 51317 |
rs556361914 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46062829 | GCATTTACTGAAGAG[A/T]AATGAAAGCAGATCT | 51317 |
rs556396806 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46073085 | TGTAATCCCAGCACT[G/T]TGGGAGGCCGAGGTG | 51317 |
rs556430292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46049676 | AACACAGCTGCAAGT[A/G]ACAAAGAGCAGCCGC | 51317 |
rs556437922 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45932100 | AGAGACGTACCCTCA[A/G]AACATGTCACTCCTC | 51317 |
rs556440856 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46017154 | TTTTGTATTTTTAGC[A/G]GAGACGGGGTTTCTC | 51317 |
rs556446738 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46025605 | TCTTATAATCTCATT[A/T]AAAAAATTTTCACTT | 51317 |
rs556466604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46057810 | TTTCTAGATGAGAGC[C/T]GACTCAGAGGTGCCA | 51317 |
rs556473028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46048827 | TTTCTTTAGGATCTA[C/T]ACCTGGAAATACATA | 51317 |
rs556512833 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:46008790 | AAATGTAAATTCAAC[G/T]GCAAAATGCTATGTT | 51317 |
rs556548685 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46039719 | AAAGACAAAAGGTCA[A/G]TATTATAAAGAGCAA | 51317 |
rs556575179 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45929897 | AGGGTGAGGATGGGA[C/G]TCCTGCTTCCTGCCA | 51317 |
rs556586748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46074977 | AAATATAAAAATTGC[A/G]GGACTGGATTTCAGT | 51317 |
rs556592270 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PHF21A | GRCh38.p7 | 11:46109591 | ATTCCCATGACAACA[C/T]ACCAGTACATTTATA | 51317 |
rs556605270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46034074 | AGAAGTAAAATGATA[C/T]CTCACTGTGGTTTTA | 51317 |
rs556606093 | snp | A/G | 0.209997 | 0.246779 | intron-variant | PHF21A | GRCh38.p7 | 11:45962672 | CAAGGCAGGTGGGTC[A/G]CCTGAGGTCAGGAGT | 51317 |
rs556607304 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46066488 | GAAGGATCACTTGCC[A/T]GGAATTCAAGACCAG | 51317 |
rs556615742 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46089211 | CTTGACAGTCATCTA[C/T]GTATCTTTACTTCTT | 51317 |
rs556651918 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46086355 | TGATCTCCTGACCTC[A/G]TGATCCGCCCGTCCT | 51317 |
rs556684201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46079967 | CGCTGCCCAAAGTTA[A/G]CAATAACCATAGACA | 51317 |
rs556690765 | in-del | -/AC | 0.326477 | 0.238015 | intron-variant | PHF21A | GRCh38.p7 | 11:45955298 | AACACACACACACAC[-/AC]ACACACACACTTTTT | 51317 |
rs556740899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46071847 | ATGTTCTCAAAGAAC[A/G]CTCAAAAATCTAAGA | 51317 |
rs556749336 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45972527 | TCACACATGTAATCC[A/C]AGCACTTTGGGAAAC | 51317 |
rs556755946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46053412 | AATCATAAATGTGCT[A/G]TACTTTCAACCTCCA | 51317 |
rs556763436 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46030347 | TCTTTCATAACAAGA[C/T]GATCCTGCACGATCT | 51317 |
rs556772737 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45983204 | TTCACAACTGCTCCT[C/G]CCCCAGGGCCTGAAA | 51317 |
rs556783409 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45969200 | AAGTCAACACTCCTC[A/G]AGGTCCAGAATGGGG | 51317 |
rs556795641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46117725 | ATTACAAATAATTTT[C/T]TAAAATACATGCTCA | 51317 |
rs556808183 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46117152 | AGAACTTTTATATGT[A/G]TTATCTCATTTGGTC | 51317 |
rs556811477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45940320 | CCTGCCTCAGACTCC[C/T]GAGTAGCTGGGATTA | 51317 |
rs556820965 | in-del | -/AA | | | intron-variant | PHF21A | GRCh38.p7 | 11:46003297 | TCAAAAAAAAAAAAA[-/AA]TGCCAAGTTTTCTTT | 51317 |
rs556826962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46089561 | CTACTGCACAAAGAG[C/T]TTGGCAACCCTGATT | 51317 |
rs556831784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46045439 | GAAAGAACAGAGAGG[C/T]TGTCTGATCCAGTGG | 51317 |
rs556865081 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45992457 | AGGCAGGAGAATGGC[A/G]TGAACCCAGGAGGCA | 51317 |
rs556868116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46054220 | AAAAAAATTTTTTTC[C/T]AAAAGGAAAAGCTGA | 51317 |
rs556869425 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46038494 | TATTCTAGGTTCTTG[-/A]AGGAGGTAAAGGAGT | 51317 |
rs556870041 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46015474 | ATTCTTATAGTTTGA[A/G]ATTTTAAAAATTTAT | 51317 |
rs556875902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46104565 | ACACTTTTATCATCT[A/G]TACTCTTTCTCACCA | 51317 |
rs556887422 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46029665 | TGCACTAGAGCCTCC[A/G]TCTCAAAAAAAAAAA | 51317 |
rs556923817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46038289 | TGTGCCACCACACCC[A/G]GCTAATTTTTGTATT | 51317 |
rs556927476 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45944788 | ATCTCTTTTTAGAGA[C/T]GGAGTCTCACTCTTG | 51317 |
rs556931072 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45978603 | GTGTTGGTTGTAAGA[C/G]GTATCCACGCTTAGG | 51317 |
rs556949842 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46022192 | TTGTGGTGGCTCATC[C/T]CTGTAATTCCAGCAC | 51317 |
rs556964179 | in-del | -/TGTTTAAAACT | | | intron-variant | PHF21A | GRCh38.p7 | 11:45977602 | AACCTAACCCAATTC[-/TGTTTAAAACT]TAAACAAAAATTATC | 51317 |
rs556970015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46037591 | TCTGTTGCGGTGAGC[C/T]GAGATCGTGCCAGCG | 51317 |
rs556988272 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46061745 | AATTATCTAAGTTTT[C/T]CCCTTCATCAAATGG | 51317 |
rs557035460 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46011979 | GATTTCCAGATGACT[A/C]TCACCTTCTTTACTT | 51317 |
rs557046377 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46008872 | CACTCCCATTCCACT[A/C]CTTATTTGACCAGTG | 51317 |
rs557047410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45971958 | TAAGGATTAGCATGT[C/T]GCCTCTGAGGTAGTT | 51317 |
rs557075346 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46021441 | CCATCAGTATTGTCA[A/G]TCTAGAAACAGTATT | 51317 |
rs557078568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45935751 | TTTGCTAAAAAAAAA[A/G]AAAAAAAAAAAAAGG | 51317 |
rs557113835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45986931 | CAAAAAGAAAGTACA[A/G]TATCAAAGCGAATGC | 51317 |
rs557149598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46055412 | TAACTGTTCTACAAC[C/T]GATGGGAAAAGTGTA | 51317 |
rs557159790 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45943724 | CTCAAAGCTATCTCC[A/C]CCACAGGAAAAAGGC | 51317 |
rs557172203 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46040551 | AGACTGGATTACTCA[C/T]TACTGCAGTACATTA | 51317 |
rs557187104 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46092096 | AGAGCCTATTTGCCA[-/A]AAAAAAAAAAAAATC | 51317 |
rs557189517 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45996660 | ACATGCTTGAGCAGA[A/T]AAAATGAAAGGCAAT | 51317 |
rs557191753 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46114154 | AACACTTAGAAAAAC[A/C]GTATTCCAACTACAA | 51317 |
rs557194470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46004651 | ACTTTTCTTCATATT[A/G]GTTTGCATAGCACAG | 51317 |
rs557196659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46097371 | TCCCTATCGCTCAAT[C/T]CTTTCCAGCAACACT | 51317 |
rs557216823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46061090 | CCATTGCTTGTTTTC[A/G]TCAGGTTTGTCAAAG | 51317 |
rs557228631 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45987061 | CAGGGCCATAATTAT[C/G]AATGCGTAAAAGAGA | 51317 |
rs557228684 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45953747 | CAAATGTGGAACATA[C/T]TAATAAAAAGGTTAG | 51317 |
rs557263417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45988615 | GCTGCTAGGCCAGGC[A/G]TGGTGGCTCACCCCT | 51317 |
rs557302457 | in-del | -/TA | | | intron-variant | PHF21A | GRCh38.p7 | 11:46099936 | ACAATTTACATTTTT[-/TA]AAAAATCTTTGTAGT | 51317 |
rs557320058 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46096542 | CTTTTGACCCACTGC[G/T]CATTTCTTCCTCCTC | 51317 |
rs557356827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46095260 | AAGATCTATACACAC[A/G]TTTGTGCTTTTTACA | 51317 |
rs557364966 | snp | C/T | 3.38295e-05 | 0.00411262 | synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45935726 | AAGTAACTTCTGTTT[C/T]TCTTCTTCTTTTGCT | 51317 |
rs557371624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46079054 | AGTTAAGTACCATCT[A/G]TATTTAAGTATTTTA | 51317 |
rs557380504 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46061975 | TTCTATACTGGAAAT[C/G]ACTGCTTTTCAGAAT | 51317 |
rs557382046 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46122085 | TGCAGCCGCAGCCGA[A/G]GCGAGGCCGGAGCCC | 51317 |
rs557395689 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PHF21A | GRCh38.p7 | 11:45961204 | GAATTTGCAACTCCT[A/G]TTCTTTTTGGTATAA | 51317 |
rs557400162 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46088824 | CTGTTCTCAAATTCT[C/G]TAAGGAGGTTCTTCT | 51317 |
rs557402231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45970566 | ATTCTTGTTCAAGTA[C/T]TTCCTCCTTAAAGGG | 51317 |
rs557428042 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:46046132 | CTCCATCTTTTGCTA[-/T]TTTTCAGGGTTTGTT | 51317 |
rs557432768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46088130 | CAGTTTATAGCATCA[A/G]AAGAATTATTGGCTA | 51317 |
rs557436875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46097192 | TAAGGTATATTCTCT[C/T]GCAAGCCAGAGTAAG | 51317 |
rs557442503 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | PHF21A | GRCh38.p7 | 11:45953009 | GTTACTATTTTCATC[A/C]CTACTTTTATGCTTC | 51317 |
rs557446471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46012742 | TCTATCTTAATATCC[C/T]ACCAACAACTCAAAT | 51317 |
rs557453510 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46114682 | TAAAATTTAAAAAAA[-/C]ACACACACAATTTAG | 51317 |
rs557470895 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46070697 | TCAAAGACTACAGAA[G/T]GGTCTATCTCTCTAA | 51317 |
rs557501234 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46036157 | TCGGAGATGAGTGAA[A/T]GGGAAGAATCAAGGA | 51317 |
rs557505987 | snp | A/C/T | 0.00756529 | 0.0611122 | intron-variant | PHF21A | GRCh38.p7 | 11:45982251 | CATAAGCCACCACGC[A/C/T]CGGCTGAGAGGTTTT | 51317 |
rs557515903 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PHF21A | GRCh38.p7 | 11:46095013 | TACATATCAGCATAG[A/G]TACACCTTTCTTGGA | 51317 |
rs557540271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46043914 | AGTAAAAGATGGATC[A/G]CAGCAACTGCTTTAA | 51317 |
rs557541178 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:45979233 | CACGTTGGCCAGGCT[A/G]GTCTCAAACTCCTGA | 51317 |
rs557545367 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46060889 | AAATCTGTGCCCATG[C/T]TTATGTCCTGAATGG | 51317 |
rs557574957 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46086411 | GGCATGAGCCACCGC[A/G]CCCAGCCAGCTATTA | 51317 |
rs557599267 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45969334 | AAGTCCTCTGTACAG[A/T]CCCCTAGCCTAAGCC | 51317 |
rs557599660 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46001814 | CCTGTTTGCATTCCA[A/T]TTTTAACTAGAGGGA | 51317 |
rs557626738 | snp | A/G | 0.000185718 | 0.00963455 | intron-variant, utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45935173 | CTGGTCAGGAAAACC[A/G]GGAAATGCAATCAGC | 51317 |
rs557626773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45944448 | TTCAAAATAAATACC[A/G]AAAAATTATGTCACT | 51317 |
rs557661865 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45949579 | TCCCATAAGAAATCA[C/G]AATCAGGGACAAGTC | 51317 |
rs557681610 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46027488 | TTCTGGGATGGGAAA[A/G]CAGTACTACCTACAC | 51317 |
rs557705549 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45929193 | GGGGTCACAGGAGGG[C/T]CTGGGCCCTTAAGGG | 51317 |
rs557707760 | in-del | -/TTAAT | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:46007714 | TAAAATTTAGTTACA[-/TTAAT]TTAAATCAAAAAACG | 51317 |
rs557734278 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46087041 | AAGATAATAATACTC[C/T]GAGCTGTCTAGAATT | 51317 |
rs557735792 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45987388 | CACCTGAGGCCAGGC[A/G]TGGTGGCTCACACCT | 51317 |
rs557747669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46044657 | TGTGCTTTCACTCAT[A/G]AACATTCTCATTTCT | 51317 |
rs557759257 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46037566 | CAATCGCTTGAATCC[A/G]GGAGCCGCCTCTGTT | 51317 |
rs557761335 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46008194 | TACGCCCATACACTC[-/T]TATCATGTGAAATCC | 51317 |
rs557766544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46044083 | CTACATTTGAGAAGA[C/T]GGTAAACTCATCATA | 51317 |
rs557769955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46026728 | AAAAACCTGAGACAC[A/G]TTGGCTTGGCAATCG | 51317 |
rs557782190 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46059881 | ACAGGCACCCACCAC[C/T]ACGCCCAGCTGATTT | 51317 |
rs557783917 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46069550 | ACACAAGGACTATAG[A/G]ATCTAACTTACTTAT | 51317 |
rs557819607 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46018722 | ACACATTTTTTTTTT[A/T]AAATTCAAGAAAACA | 51317 |
rs557826701 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46047492 | AACCGAGACAAAAAG[G/T]TAAATGACTTTTAGT | 51317 |
rs557856987 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46080319 | GCACACCAGCACACC[C/T]GGTTAATTTTTTAAT | 51317 |
rs557859186 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46019607 | ATTGCACTCTATTCA[C/T]CTGTGACCAATTTTT | 51317 |
rs557868295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45978500 | CTTGCAAAATGTTGC[A/G]CATGAACCAGTCCAA | 51317 |
rs557908783 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46062092 | CTGTTTTTTGTTTTG[-/T]TTTTTTTTTTTCCTC | 51317 |
rs557994083 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46121984 | AGTGCAGCGGCGGCG[A/G]CGGCGGCGGTGATGG | 51317 |
rs558005240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46035388 | TGCCAGCATCATACC[A/G]TTCACTGACTAAACC | 51317 |
rs558014830 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45981505 | ATGGCTCATAAAGCA[C/T]ATAATAACTATTTGG | 51317 |
rs558018230 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45960251 | ACAGCAGAACTATGC[A/C]CAATAGCCAAAAAGT | 51317 |
rs558046024 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:45967369 | TGAGACCCTGTCTTA[-/A]AAAAAAAAAAAAAAA | 51317 |
rs558051599 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46016266 | GAACAATCTTTCTCA[A/G]AAAGGGATATCACCA | 51317 |
rs558066901 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45984751 | AAGAAACTCCAAGAC[A/C]CTGCCCTCCACAACT | 51317 |
rs558069155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46042606 | GGACATGGTGCTAGA[C/T]CTGAATGTTTGTGTC | 51317 |
rs558086760 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45995507 | CCCGGGTTTATAAAA[G/T]ATCAGAGCACTTGTC | 51317 |
rs558088841 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46005392 | AATATTTGCACAATA[A/T]ATTAACGCCTTGTAT | 51317 |
rs558121887 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45996037 | TAACCTCAAACTCCC[C/T]GGCTCAAGTGATCCT | 51317 |
rs558192948 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45968231 | TATTCTCTGCACAGA[A/G]GCAAGAAGGAATTTT | 51317 |
rs558245647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46019463 | CACACAGCCCTAAGA[C/T]GTGGCCAATCCAGGC | 51317 |
rs558256455 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46120246 | GTTTTCCAAAAAAAA[A/T]TTTTTTTTAATTAAA | 51317 |
rs558308854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45994215 | CAACATTTAGACTGG[A/G]TAAAGTGTTGGGCTC | 51317 |
rs558309794 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45990742 | AGAAGACTTTATTTT[G/T]AGAGCAGTTTTAGGT | 51317 |
rs558317121 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46091930 | GACATTTTTGGAAAA[C/T]GGGACTTTTACATTT | 51317 |
rs558333391 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45969189 | TCCTACCAAGGAAGT[A/C]AACACTCCTCAAGGT | 51317 |
rs558391384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46015759 | CAATATTACTGTCTT[C/T]TACCTCTATACCTTA | 51317 |
rs558401024 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45933871 | AGAACCAAAAGAATT[C/T]TGCACTTTCCAGAAA | 51317 |
rs558418813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46101763 | AACTCAGCCTCCCTA[A/G]TAGCTGGGACTACAG | 51317 |
rs558460877 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46099282 | CTGATGGAGCCCTCA[C/G]TATACTACAGTCCTT | 51317 |
rs558463437 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:45976826 | GTCAAAGAGCCAGAT[C/T]CTGTCTAAAAAACAA | 51317 |
rs558474848 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46115210 | CCACACAAGTCTAGT[G/T]TAAGAAAGTTGCTTT | 51317 |
rs558483751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46047639 | GATATTATTTTTTCT[C/T]TGCAATGTTCTGACA | 51317 |
rs558486673 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46015059 | GACTGGTGTAAAGTG[C/G]TATCACTGTGCTTTT | 51317 |
rs558495303 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46094404 | GTCACTCAGCTAGCT[C/G]ATAGTGAAGCTGGAG | 51317 |
rs558498082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46107486 | TTGGCTGGTAAAAAA[C/T]GTTGACTACTCTATA | 51317 |
rs558512932 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45960252 | CAGCAGAACTATGCA[A/C]AATAGCCAAAAAGTG | 51317 |
rs558521271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45998405 | TATGCCTACTGAGTA[C/T]ATAGTATTGTAACAG | 51317 |
rs558543641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45973284 | ATCACTGTGCAATAC[C/T]AGTGAAAAGTACCTC | 51317 |
rs558593405 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45965036 | TGACGGAGGGCAGCA[C/G]AGCCTGTCTGTGAAT | 51317 |
rs558606829 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45947066 | ATCTCTAAAAATTGG[C/G]GCTGTTTAAAAGTCT | 51317 |
rs558611429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45982104 | TGGGACTACAAGAGC[A/G]TGCTACCATGCCCAG | 51317 |
rs558614332 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:45960184 | ACTCCTAGGTATATA[-/C]CCTAAAGAACTGAAA | 51317 |
rs558629943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46105634 | AAAAAACACAAAAGG[A/G]ATGAATGAGTCTAAG | 51317 |
rs558632749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45998815 | ATGAGCCACCACACC[C/T]GGCCTTTTTTTGTTT | 51317 |
rs558641354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46008025 | GGTACTAAAGTAAAA[C/T]GTGTTTAATGTTGTT | 51317 |
rs558658799 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46073879 | CTGCCAGAGTTTCTT[C/T]CAGAAATCTCAAGTT | 51317 |
rs558712513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45980697 | ATTTTTTGCATATGA[C/T]AACACAGATACTAGC | 51317 |
rs558719232 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46114474 | GCACACAAATTTAAC[A/G]CAATCCAGCTAAAAA | 51317 |
rs558722094 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46088659 | TACTTCATAAGACTG[C/T]TGTGGTTTAAATAAG | 51317 |
rs558726862 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46038862 | AATCACCTCTTAAAG[G/T]CCCCATCTTTCAGTG | 51317 |
rs558734020 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45961987 | GAAGTTGGTTATGTC[C/T]GACAGGGGAAGGACA | 51317 |
rs558745072 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46098536 | TTGCTTCCTCACTCT[A/G]TAAAGTACAAAAATC | 51317 |
rs558754903 | snp | C/T | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45931080 | CAAAACAGCTCACAT[C/T]TGAATGTCAGGAAGA | 51317 |
rs558775292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46089760 | TCTAAATGTCTGAAT[A/G]TATGTGAGTATAAAA | 51317 |
rs558820555 | snp | C/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930741 | CAGTGGGCAGCCGCT[C/G]CAGCTCTCTGAAGTG | 51317 |
rs558859243 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46082235 | GAACACATTTTCTAT[A/C]CAGTAAGCTCAATTT | 51317 |
rs558864821 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46070993 | TATTTGGAGATACAT[G/T]GTTAAAAATTTTTTT | 51317 |
rs558892005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:46090538 | GAGATTCACAATGCA[C/T]ATTAGCATATTAAAG | 51317 |
rs558899371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46062300 | TTTTCTCTTCTCCAT[C/T]TTCTCTGTTCCCTTG | 51317 |
rs558901403 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46071945 | ATAAGCAGAGCAAAA[C/G]ATCGGGTGGATAAAA | 51317 |
rs558922647 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45972715 | GGTCAGGAGTTCGAG[A/G]CCAGCCTGGCCAACA | 51317 |
rs558928718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45945338 | ATTTGACAGTTTTTC[C/T]GGAACCTGTTTCTGA | 51317 |
rs558932644 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46020755 | CCTATAAAGCCATGA[C/T]AGTTATGGTTGAAAA | 51317 |
rs558933024 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46097095 | TCTCCTACCACCTCC[C/T]TGGTCCAAGTCACCT | 51317 |
rs558950019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45936932 | AGCCACTGGCAGTTT[C/T]GTCCTTGACCTGACA | 51317 |
rs559007027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46054449 | AAAATCCACTTACCT[A/G]CTCCTACACATCTTT | 51317 |
rs559008198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45945576 | CCATCTGTTTTCTGA[A/G]AACTCATTCACAGTA | 51317 |
rs559060212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46062886 | TCAAATTAATGTTAT[C/T]TGTAACAGCTAAAAA | 51317 |
rs559061568 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46021411 | TTAAACTATTAACAA[C/G]TATACACCATACCTC | 51317 |
rs559068328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45944915 | GGGATTACAGGAGCA[C/T]GCCATGCCCGGCTAA | 51317 |
rs559096012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45962884 | GGCGACAGAGCGAGA[C/T]TCTGTCTCAAAAAAG | 51317 |
rs559131353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45984636 | CTTTTGTCAACAGAG[A/G]AGGGAGACGGAGAGA | 51317 |
rs559133517 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PHF21A, LOC105376661 | GRCh38.p7 | 11:46123410 | CTTTATGGTACATGT[G/T]TAGGCCATTTAGTAG | 51317 |
rs559133951 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45960032 | AAAAGGAAAGTAATA[G/T]GTGTGGTAAGGATGC | 51317 |
rs559146063 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45994213 | GGCAACATTTAGACT[-/G]GGTAAAGTGTTGGGC | 51317 |
rs559187294 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46071276 | CCCAGGTAGCTGCTG[A/T]CCCTTCATGCAAGGC | 51317 |
rs559193599 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45994717 | TTTCAACTCTGTGCT[C/G]AGCTGGCAAAAGCTC | 51317 |
rs559229090 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46060075 | AAATTTATGGAACAG[-/A]AAAAAAAGACTTAAA | 51317 |
rs559276954 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46055244 | GCAAATTTTTAGTAA[-/T]TTTTTTTTATCATTT | 51317 |
rs559285475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46028259 | CATGTACTCAGGACT[A/G]TCCCTGAACTTTTAA | 51317 |
rs559307316 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45974241 | CCCAGGTAGTGCTTA[C/G]ATCTTTACCCCTACT | 51317 |
rs559311392 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45953154 | AGCTGAGTGAACTAG[A/G]TATCTTATAAATGTT | 51317 |
rs559314818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46087718 | AGAAGGGGTCTCATA[C/T]GTTGCCCAGGCTGGT | 51317 |
rs559348570 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46013833 | CTACAGTAAAAATAC[A/C]CTACGAAAGATGAAA | 51317 |
rs559350005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46054709 | TGCCACTAGAAGGTA[A/G]GTTCCTTAAGAAGAG | 51317 |
rs559367392 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45981970 | TTTTTTTTTTTGGTT[A/G]TTTTGAAACAGGGTC | 51317 |
rs559377339 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46114676 | ACTTATTTAAAATTT[A/T]AAAAAAACACACACA | 51317 |
rs559408678 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46036856 | TACATCTGTTGTTTA[A/C]ATAGCATTTTTTATG | 51317 |
rs559414059 | in-del | -/T | 0.0150606 | 0.0854603 | intron-variant | PHF21A | GRCh38.p7 | 11:45991273 | ACAGTAGTACCTTGA[-/T]TTTTTTCCATATGGT | 51317 |
rs559419768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45950788 | CATACTCACAAAACA[C/T]GCAGAGAGTTTTAAA | 51317 |
rs559422345 | in-del | -/AAC | | | intron-variant | PHF21A | GRCh38.p7 | 11:46117662 | TATTATAGGGATGAT[-/AAC]AAGGCTTAAAGCCCT | 51317 |
rs559429061 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45941462 | AATATCTGGTAAACC[C/T]CACTGTTCGGTCTTG | 51317 |
rs559461388 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46029087 | TGTAGCTTGCAAAAG[A/T]GTGTTATCTGTCATG | 51317 |
rs559492982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PHF21A | GRCh38.p7 | 11:45934739 | GCAGCATTTAGGAGG[A/G]TCGAAGCCCCAAGGA | 51317 |
rs559507746 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PHF21A | GRCh38.p7 | 11:46006832 | TGGAATAATATTTCT[A/G]TTCTTTCCTTCAAAG | 51317 |
rs559563455 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46050480 | AGCTGCCGAATCACA[A/G]AAAGCAACAAGAAAT | 51317 |
rs559569995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45962279 | TATTTAGCCTGGTCA[C/T]AGAGAGAACGTTGGA | 51317 |
rs559574550 | snp | A/G | 0.140242 | 0.224618 | intron-variant | PHF21A | GRCh38.p7 | 11:46021074 | TTTAAAAAAAAAAAA[A/G]AGAGAGACAAGGTCT | 51317 |
rs559585143 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45970021 | CTACAAGCTTTCATC[A/G/T]TAAGTTAATCATCTG | 51317 |
rs559598181 | snp | A/C/T | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46048626 | AATACAAAAATTAGC[A/C/T]GGGCATGGTGGCATA | 51317 |
rs559632568 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46003958 | ATCTTTATGAAAATA[C/T]GTATCATCCTCAGAA | 51317 |
rs559634144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46012054 | TCCCTCACACTAGAC[C/T]CCTTTTCCTTTTTAC | 51317 |
rs559640418 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46082780 | TGAAACAAAATATTT[A/G]GTAATTAACTTCAAT | 51317 |
rs559643942 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46089395 | TTTATTAAAAACTTT[A/C]ACATTTATTAACATG | 51317 |
rs559655574 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46115836 | TAAGGATACAAAATT[C/T]AAAAGCACATTAATA | 51317 |
rs559675326 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46120476 | GCCGCCTCTGTCACC[C/G]GCTCCGGCCCTGCAC | 51317 |
rs559689481 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45995799 | TAGACAAAAACAAAC[A/C]AAAAACATAAAGCTG | 51317 |
rs559720771 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46052860 | CTTACCATGATGAAT[A/C/G]AGCAAAGGCATCACA | 51317 |
rs559738514 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46103964 | ACTCCTCAAATCTGA[A/G]GAGATCATTGTACCT | 51317 |
rs559739270 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46014342 | CTGCAAAGGATATTA[C/T]GTTGTTCTTTTTTAT | 51317 |
rs559740181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46112736 | TTCCATCCAACCTTA[C/T]GGAACAACTATCCCC | 51317 |
rs559745697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46000667 | TCTCACGTCTGTAAT[C/T]CCAGTACTTTGGGAG | 51317 |
rs559757654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46052027 | GAAAACAGTCAAAGG[A/G]ATAGTCAATAGTCAA | 51317 |
rs559774016 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46112004 | ACTAGTTTGGATATT[C/G]TAACAGTGCAAACAT | 51317 |
rs559798895 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45987497 | AAACTCCGTCTCTAC[A/T]AAAAATACAAAAAAT | 51317 |
rs559812884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46032332 | TAATATTTTTCTGAT[C/T]TTATATAACAATCTG | 51317 |
rs559844192 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46060225 | CTGGTCTCAAACTCC[C/T]GGCCTCAAGCAATCC | 51317 |
rs559850728 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45932412 | CCTGCACCAAGAAGA[A/G]AGCACGGTCTTTTCT | 51317 |
rs559853460 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46041288 | ATAAAAAGTAAGGAG[C/G]GTGGAAAAGATAAGT | 51317 |
rs559884879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45991929 | TGAAATCTCACTCAC[A/G]TGAACATGTAAACTG | 51317 |
rs559887621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45960543 | CGGCAGAGGGCAAAA[A/G]TTAAATAATTGCTTA | 51317 |
rs559905470 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46095943 | CAGAAGATTCAATCT[C/G]TTCTCTTCCCCTTAC | 51317 |
rs559939162 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46018852 | CTGCATACCATGACA[C/T]GCTCTCACAGATGCA | 51317 |
rs559967589 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46122216 | ACAGCAGTTTGAAGG[C/G]GGGGGGGGAAAGCCG | 51317 |
rs559971290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46068981 | TCTTTCTCAAAGAGA[C/T]AGTAAAATCTTTGAC | 51317 |
rs560011183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45983384 | CTTTCTTTAAAAGAT[A/G]GCGTTGGTATGTCAA | 51317 |
rs560034097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46009119 | AGCTGGGATTACAGG[C/T]GTGCATCACCATGCC | 51317 |
rs560053105 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | PHF21A | GRCh38.p7 | 11:45943149 | TTTTTTTGAGACAGG[G/T]TCTTGTTCTGTCACC | 51317 |
rs560100609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45956093 | TTCTTCAAAAATGGA[A/G]AAATTAAGACATTCC | 51317 |
rs560107146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46090960 | AAATGGGTTAAGGTC[A/G]CTTCTCTAAGATTCC | 51317 |
rs560113058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45972977 | CAGCTACTCGGGAGG[C/T]TGAGGCAGGGGAATC | 51317 |
rs560122608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45991096 | TGCCTCCATAGTTCT[A/G]CCCTTTCCAGAATGT | 51317 |
rs560143166 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46100526 | TTCTTAAGTATAATT[G/T]TTAAAATATATATCT | 51317 |
rs560192506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46041998 | AAATCCTGTATGTCT[A/G]TTTAAGTGTTAAAAA | 51317 |
rs560210643 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46067567 | TAAAACACTGAAGTA[C/G]GAAATAATAATAAGA | 51317 |
rs560247776 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45973440 | TATGCGCATATACAC[A/G]TATTATCTAATCTTT | 51317 |
rs560248097 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:45974772 | GATTTATTTATATGA[A/G]AGCTGTGATTTGTTT | 51317 |
rs560268355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46106785 | GGCACTGCCATCTCA[A/G]TGGGAGTAGAAGCTA | 51317 |
rs560268505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46097640 | CTAACTATCCAAATC[C/T]CACCCACACACTAGG | 51317 |
rs560281590 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46116719 | CTATAATCCCAGCAC[A/T]TTGGGAGGCCAAGGC | 51317 |
rs560295863 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46082320 | ACTATTTCGTCAAAT[A/G]TATGTTCTGGCTTTG | 51317 |
rs560303018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46101217 | TGTCCAGCAGGCATC[A/G]TTCTTCACTAAGTTA | 51317 |
rs560324441 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46077433 | GATGAGATACACAGA[A/G]CATGATTGCCTTTTA | 51317 |
rs560353598 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46105882 | TTAAAACAAAAAACA[A/T]GACTATTGCAGTATA | 51317 |
rs560356857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46048546 | AGGCCGAGGCAGGCA[A/G]GTCACCTGAGGTCAG | 51317 |
rs560360673 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46023261 | TTCCATAAGGCAGGC[C/T]GGGATCTGGCAGAGA | 51317 |
rs560373918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45981250 | AATTAGCCAAGCATG[A/G]TGGCACACACCTGTA | 51317 |
rs560383935 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46103410 | AATTATTTAATTGAA[A/G]GATAACTATACAACC | 51317 |
rs560384885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46082527 | ATAAATAAATGTTTA[C/T]AATCACACAAGCAAA | 51317 |
rs560431126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46098700 | ATCAGTTAACCTCAG[A/G]ACTAAAACTCTTGTC | 51317 |
rs560461611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45948590 | TTTACATGGGGTTCT[A/G]TTCACTGTGCTATTC | 51317 |
rs560475069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46066342 | CATACATATAAATAT[A/G]TATTAGATATTTATC | 51317 |
rs560476791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45947416 | TTATATTAGGATTAT[A/G]CACAAGAGTCATGAT | 51317 |
rs560481781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46031558 | TAGTTCATGCAGCCG[A/G]TACGAATTCATTCTT | 51317 |
rs560490922 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46030684 | AAACATAATAAAACC[A/C]ATTTTCACTAAATCT | 51317 |
rs560502386 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46020894 | TTATGATGGGGTTAT[A/G]TCCTGATAATTCCAT | 51317 |
rs560503625 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46022609 | TGGGACTACAGGCAC[A/G]TGCCACCATGCCAGT | 51317 |
rs560510601 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45998983 | AGGCACCTGCCACCA[C/T]GCCTGGCTAATTTTT | 51317 |
rs560534663 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46073455 | CTTGATGTTAAAAAA[A/T]TTTTTTAAATCTTAT | 51317 |
rs560551276 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45960919 | TTGAAGAAGTCTCCA[C/T]GTGATAAAAGTTTGT | 51317 |
rs560566321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46089908 | TGGGCCAGGCCAGGG[C/T]TCCCCATAGCACCCT | 51317 |
rs560569258 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46073062 | ACACTTCAGCATTAC[A/C]TCACGCCTGTAATCC | 51317 |
rs560608473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45955433 | CTCTTTGAATAGGAA[A/G]GAGAGAAGTATGATG | 51317 |
rs560614372 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46014630 | CCCACCAACAGTATA[A/T]GTGTTCCCTTTTTTC | 51317 |
rs560625215 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45990106 | ACAAAATCTAATCCA[C/T]AAATTTCTACACAAA | 51317 |
rs560642394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46040421 | CAAAATAACTTAGCA[A/G]TCTAATTATAAGTAG | 51317 |
rs560671963 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45964574 | CTTTTTAAAGCAACT[G/T]TCTTGAGAGAGAATG | 51317 |
rs560679212 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46048338 | GTATCATTCTATATG[G/T]AGTACTTCATTCCTT | 51317 |
rs560694025 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930309 | AACCACCTCCATGCA[C/T]GCTGCCTGTTGGGCC | 51317 |
rs560703987 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46067093 | ACCTTATGTATTACT[C/T]ACTTATGTATTACTT | 51317 |
rs560727835 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46116592 | TAAATTATGAGAAAC[G/T]GACTAGGCAGCATTT | 51317 |
rs560728163 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46002059 | AGTGACTATTTTTAG[C/T]GAAAACAAAACAGTA | 51317 |
rs560742405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46056338 | TTTCACTGGCTTGGG[C/T]TGTGTGGGTCAGTTT | 51317 |
rs560762927 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46046059 | CTCAGCTTTGTGAGC[C/T]CTGGCATTCAGCTAG | 51317 |
rs560767159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45998597 | GGCTCGGCGCAACCT[C/T]CACCTCCCAGGTTCA | 51317 |
rs560772398 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46026954 | TTGGAACACAGAAAA[G/T]CTGCTTTTGCTAGCA | 51317 |
rs560776975 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46101319 | TAAACTAACAATGTA[A/T]GAAAAGAACATTCTC | 51317 |
rs560789241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46022535 | GGCATGATCATGGCT[A/G]ACTGCAGCCTCAAAC | 51317 |
rs560792981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46038504 | TCTTGAAGGAGGTAA[A/G]GGAGTCAGTTGTGTG | 51317 |
rs560839573 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46102843 | AGCTTAAGGTTTTGA[A/T]AATAGCTCAGTATCT | 51317 |
rs560841455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46064016 | AATTTCAAGTTCTGT[C/T]GATTAACACCCTCCC | 51317 |
rs560858296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45939034 | GAGACGGGGTTTCAC[A/G]TGTTAGCCAGGATGG | 51317 |
rs560867839 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46105555 | AAAATGAATGTCACT[A/C]TGAAAATATCCCAGT | 51317 |
rs560880095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46099819 | CTGTTTCCAGCCTGA[A/G]AGAAAATTAGAATCT | 51317 |
rs560923248 | snp | A/G | 4.9516e-05 | 0.00497549 | intron-variant | PHF21A | GRCh38.p7 | 11:45979976 | TCTTTTCTACCAAAT[A/G]AAGACAAAAAGAAAT | 51317 |
rs560944863 | snp | A/G | 1.67556e-05 | 0.0028944 | intron-variant | PHF21A | GRCh38.p7 | 11:45938325 | ACCCTATAAAGTTGA[A/G]AGGAAAGGTAAGAAA | 51317 |
rs560967418 | in-del | -/AACT | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46046408 | AAAAGAGAAACCAAA[-/AACT]AAAACAAACCAAACC | 51317 |
rs560982404 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45989066 | TCGTCAAACAACAGG[C/G]AGGGTGCAAGTTCCT | 51317 |
rs561008257 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46019219 | AACTGCTTTTTAATT[A/C]TTTCTAGAAGATAGG | 51317 |
rs561025976 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46021705 | CACCACTATGCCCAG[C/G]TAATTTTTATGTTAT | 51317 |
rs561059454 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46099922 | AAAAATGGTTCCATA[A/C]AATTTACATTTTTTA | 51317 |
rs561102597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46105007 | TAAGCTTCAGTACCA[C/T]TTATTTAGTACTTAC | 51317 |
rs561104456 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PHF21A | GRCh38.p7 | 11:46114581 | CAACATACTGTCCAT[A/G]AGGCCAGAGATAGCA | 51317 |
rs561120445 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46098603 | TTTCTGAGTCTAATG[A/C]TCATAACGAAAACTT | 51317 |
rs561167338 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45998875 | TTGCCCAGGCTGGAG[G/T]GCAGTGGTGTGATCT | 51317 |
rs561177488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45972842 | TTGCTTGAACCCGGG[A/G]GGCGGAGGTTGCAGT | 51317 |
rs561191561 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45955159 | TTTTATGCACCTCTT[G/T]TTTTTGCATCCCTTT | 51317 |
rs561196873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46055702 | GAGTCATGGAATCTC[C/T]TTATATAAACGCCCC | 51317 |
rs561204305 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46030564 | TCATTAGTCTGTTCT[A/C]TGAATGTTACTAAAA | 51317 |
rs561211812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46073323 | ACAAAGCGAGACCCC[A/G]TCTCAAAAAAAAAAA | 51317 |
rs561226021 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46056151 | TAATTTAATGCCTCC[A/G]GTTTTGAATTTCATC | 51317 |
rs561232713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46089817 | GAGGGGGTGGGGGGC[A/G]GGTCCTCATTTTTTA | 51317 |
rs561250445 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45939518 | AAGCAACAGCTGACA[A/G]TGTTCTCCTAAAACC | 51317 |
rs561251531 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46007482 | CCATGTCCAGCTTAT[G/T]TTTGTATTTTTAGTA | 51317 |
rs561270411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45988385 | CGTAGCAGGCAGTAT[A/G]TATCATGTAGAAAAT | 51317 |
rs561279535 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930265 | AGCGTGCTGCAGACA[C/T]GGTCACCCTCACGGA | 51317 |
rs561287820 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46006752 | CTTAAACGCCTATTA[C/G]AATGTGATATACTTG | 51317 |
rs561302197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46030089 | GTTGTTATTCATTAC[A/G]GTCTTTGGACAAAGA | 51317 |
rs561330725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46089161 | CAATGTTTAAAGTAG[A/G]TTTAATTCATTTTTT | 51317 |
rs561340467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46038443 | CATTTCATTCTTTCA[A/G]TAACTATTTATTGAG | 51317 |
rs561341786 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46062823 | ACTAAGGCATTTACT[A/G]AAGAGAAATGAAAGC | 51317 |
rs561365260 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46097533 | AAAAGAATACTAAAA[C/T]AAAGACTAAAACTAT | 51317 |
rs561370471 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:45989005 | TACAATCACTTAAAG[-/A]AAAAAATGAACAATG | 51317 |
rs561379108 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46080470 | ACTTCTTAAAAAGAA[A/G]AAAAAAAATTTAAAA | 51317 |
rs561383622 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45963212 | GTCGCCTGAGGTCAG[C/G]AGTCTGAGACCAGCC | 51317 |
rs561403382 | in-del | -/ACTA | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:45940358 | CCACCACCACGCCTG[-/ACTA]ACTTTTATATTTTTA | 51317 |
rs561464413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45945367 | GATCAACTCTGCTCT[A/G]AAGAGCAGAGTTTCT | 51317 |
rs561502367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46101450 | AGATTGGCAAAATGC[C/T]GGTAATTGTTAGTTA | 51317 |
rs561502520 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46111106 | ACAAATTTTAAATCA[C/G]AACTATGTGGGGGGG | 51317 |
rs561542099 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45929610 | GGGCTGAGGACCCAC[A/G]GACACCGGAGAGAGG | 51317 |
rs561589613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46110320 | GGAGTACACTTAAGA[C/T]CAAGTCTTCTGACAT | 51317 |
rs561597626 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46045285 | ATTTCTTTTTCCCTA[G/T]GAAAGATCATAAGCA | 51317 |
rs561599825 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46054632 | ATCAAAGACTAGATC[G/T]TATTACTCTACAACT | 51317 |
rs561600395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45959780 | CGGAACAGGAGAAAA[C/T]ATTTGCAAATCATGT | 51317 |
rs561604070 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | PHF21A | GRCh38.p7 | 11:46018461 | AAATCTATAGGGGAA[A/T]AAGAAAAGAATCTCC | 51317 |
rs561634526 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46035841 | AAAAGAGAGGTTGGA[A/G/T]AAAGTAGGTATGTAT | 51317 |
rs561663631 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45936073 | ACTTGAGCCCAGGAG[A/T]TTGAGACCAGCCTGG | 51317 |
rs561665949 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:46101936 | AATCTCGGCTCACTA[C/T]AACCTCTGACTCCTG | 51317 |
rs561668041 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45967994 | ACAACAAGTGGGTCA[G/T]GATCCACTGTTTGAA | 51317 |
rs561690089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45941516 | AATGATGGTTTAGTA[C/T]CATTATGAAAATAGC | 51317 |
rs561721904 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PHF21A | GRCh38.p7 | 11:45992923 | CCTCTACCACTGAAC[C/T]GCAGCTACCTCAAGT | 51317 |
rs561737056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45957464 | ATGGAAAAAAACTAG[A/G]AATTAATGACAGCAG | 51317 |
rs561739463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46077066 | ACATGAAGTTTTATA[C/T]TTGAGCATCTTGTAC | 51317 |
rs561756586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46050082 | TTCCCCAGCAGAGTT[A/G]GCGATTGCCACTAGG | 51317 |
rs561758841 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46001718 | TATGATAGGCCATGG[A/G]AGAATAAAACCAATA | 51317 |
rs561763116 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46020054 | AAAACAAAGATACTA[C/T]TGTGAAGGCAGGTTT | 51317 |
rs561768521 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46076416 | AGGTAACAAGGTACA[C/T]GCAGCACCTACAAGA | 51317 |
rs561802017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46026927 | AGGTCCACTGGAGAG[A/G]CTGTTGAGTGTTTGG | 51317 |
rs561805713 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930981 | GGGGCCTCTTCTTTA[C/G]AGTAAAGCAGTGTTT | 51317 |
rs561815123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45949263 | AAAAATGATAAGTCA[A/G]AAAAAATCTACCACT | 51317 |
rs561817862 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45971973 | CGCCTCTGAGGTAGT[C/T]ACCCTGGAGGCAATG | 51317 |
rs561830556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46086683 | ATGTGTCCAAAATGA[C/T]TCCTTATAATTTTTG | 51317 |
rs561876912 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45948814 | TATAATGATGGGAGG[A/C]GGGAAGGAGAAGAAA | 51317 |
rs561895659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46067299 | ACAAGTATCTGAAAA[A/G]TCTAGAGGGTAAGGT | 51317 |
rs561910641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46002531 | TATTTGGGGGAAAAA[A/G]AAAGGAATTCACACA | 51317 |
rs561942921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46059180 | GTACAAATATTTACG[C/T]CCAAGGATGTACACT | 51317 |
rs561949536 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46041128 | AAACATGTATAAAAA[G/T]CCACCTTCTTATTCT | 51317 |
rs561954186 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46042798 | TAGCACCTTCTTGCT[A/G]TGTCCTCACAGCAAG | 51317 |
rs561990398 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46042379 | GCCATATTAGTATGT[A/G]TGATAGTGCAACTCC | 51317 |
rs561997392 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46009209 | CAACTCCCGACCTCA[A/G]GTAATCTGCCCGCCT | 51317 |
rs562000032 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46058374 | CTTTGAAAGGATATT[C/T]TGAAGGGCAGTTCAA | 51317 |
rs562013167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46009270 | TGAGCCACTGCGCCC[A/G]GCCATTAGTTCACAT | 51317 |
rs562015003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46017267 | TGAGCCACCACGCCC[A/G]GCCTACATCTATTAA | 51317 |
rs562017529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45993839 | TCAGAGATGAGGCTC[A/G]GGCAGCTGGCGAGAT | 51317 |
rs562026218 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45998501 | GTACATGCAAAATAA[C/T]TCTACCATTTCTTTT | 51317 |
rs562048566 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45955865 | TGAAGAAGTGAGGTC[A/T]GCCAACAACCATGTG | 51317 |
rs562062273 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46031720 | ACTCTTTTTTCCTCT[A/G]GCTTTGTCTGTTAGG | 51317 |
rs562098139 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46107218 | ATCATACATTTAACT[A/G]GTAACCATAATTTTT | 51317 |
rs562098809 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46066682 | CCAGCTTGGGCGACA[A/G]AGCAAGACCTTGCCT | 51317 |
rs562101166 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45966899 | TGGGATTACAGATGT[A/G]AGCCACTGCACCCAG | 51317 |
rs562103494 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46016570 | CCCTTCCCTAATCCC[C/T]TACTCAGGATTAATA | 51317 |
rs562123363 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46114133 | CACACACACGCTTCT[A/G]CAAAGAACACTTAGA | 51317 |
rs562138908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46091737 | CTTTTTTTAAGAGAT[A/G]AGGGTCTCGTTTTGT | 51317 |
rs562157863 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46000196 | ACATATTTAGCACGA[A/G]GAAACTGCTACACTA | 51317 |
rs562166063 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46032013 | CAGCTTTATTAGCTG[A/G]TAATTTAAAACACAG | 51317 |
rs562178409 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45992817 | ATACGTTTCATAATG[C/G]TGCCTACTTTATCAA | 51317 |
rs562179089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46010066 | TTTAGTTGCTTAACC[A/G]TATCATACTAAAAGA | 51317 |
rs562197905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45966517 | TTAAAAACATGAGGT[C/T]AGCCTTGCTTGGGTT | 51317 |
rs562224702 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46024057 | ACAGTTTGGGAAATA[A/C]TGGATTAGTTGCAAT | 51317 |
rs562229112 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46088686 | TAAGGCAAAATTATA[A/T]GAAAAGCCCTTTGCA | 51317 |
rs562242801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45983304 | GTCCTTGAGAGGAGG[A/G]AAAAAAAAAAGGAAA | 51317 |
rs562257784 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45974614 | AGGTGCTACCACACC[C/T]GGCTAATTTTTTTTA | 51317 |
rs562261184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45984803 | CTGCTTTTTCACACA[C/T]TCAGTCACTCCACTG | 51317 |
rs562296723 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46070821 | TGGACAAACGGCAAA[A/T]TCTTTGAAAAATATA | 51317 |
rs562300160 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46100341 | AGCATGGGGTCCCAT[C/T]AGGCACCCTATTTTA | 51317 |
rs562306990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45982520 | TTCTATTTCTCCAAT[A/G]TAAAAGGCAGAATAA | 51317 |
rs562321892 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45932267 | GTGGCTGAAAGACCA[A/G]AAGCAGCACCAAAGG | 51317 |
rs562330701 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45950129 | ATTTTCTATTCCAGG[A/T]ATTCAATCAAACATC | 51317 |
rs562332988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46118451 | GCCCCTGGAATATTC[A/G]TAACATGTTAGCCAG | 51317 |
rs562337758 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45933548 | GACTTGTCTTCTCTA[C/T]CTAAACAAACGGCTC | 51317 |
rs562341944 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46091129 | CCCAGTCCCCAAAAG[A/G]AAGAGAGACACCACA | 51317 |
rs562343970 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45991730 | TACCCAATCTTGGTC[A/T]CAGCTTCTGCACTCA | 51317 |
rs562344619 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46092510 | CACATAGAAATGAAA[A/T]GCACCTCATTTAAAT | 51317 |
rs562382414 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46003788 | TTAAAAGCTTCATTA[C/T]ACTCTGCAGACATTT | 51317 |
rs562392608 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46005196 | ATCCAAAACTTTTTG[A/G]GCACTGACGTGATGC | 51317 |
rs562466230 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46110044 | TAATTTTTTGGTTCT[A/C]ACTCATTATTTAAAA | 51317 |
rs562476055 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46033399 | CCTCCCAAACAGCTG[C/G]GACCACAGGTGTGCA | 51317 |
rs562492025 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PHF21A | GRCh38.p7 | 11:45933452 | CCCTCTTCTGGGCAC[C/T]GGGGTTGGTGAAATC | 51317 |
rs562503815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46101817 | ATTTTTGTATTTTTT[A/G]TAGAAACAGGGTTTC | 51317 |
rs562533951 | snp | C/G | 1.66341e-05 | 0.00288388 | synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45965477 | GTGGATGGAATTCTG[C/G]GATGTGGGAAGGGTT | 51317 |
rs562542900 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46085534 | CAAAAGTCTGTTTTT[C/G]CCTGAATAAATTTAA | 51317 |
rs562558778 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46106048 | GGACCTAAAGGTACT[A/G]AGAACCTGACACAAT | 51317 |
rs562559733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45976375 | AAAATAGAAACTCTC[C/T]GATTTGTGAATTTAG | 51317 |
rs562581566 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46084928 | CTCGTGATCCACCCA[C/T]CTCAGCCTCCCAAAG | 51317 |
rs562600606 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46034634 | GGTGACTATCCAGCT[A/C]ATGACAGGTCTCCCA | 51317 |
rs562612586 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46093302 | TTTGTTGACTGATAT[C/T]ACTCCAATAGTGTCT | 51317 |
rs562636880 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46042754 | TAAAAGAGGCCTATG[A/T]AAGCTTGTTTTTCCC | 51317 |
rs562653063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46057448 | CATTAGGGCTTAATT[C/T]TCCCAATGAACCCAG | 51317 |
rs562659488 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46009751 | TTAGTCACTGCACAA[G/T]ACAATTAATATAATT | 51317 |
rs562659777 | in-del | -/TTAT | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45932901 | CAGCTTTTCTATTCC[-/TTAT]TTTAGTTTTTGTTAC | 51317 |
rs562670422 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45956268 | CTAGATGAATAAATA[A/T]AAAAGCCAGTGTTAT | 51317 |
rs562687277 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45939979 | GAAGGTCTAATACAG[A/C]AATTGTGCACAAGAA | 51317 |
rs562703036 | snp | G/T | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45931313 | TGGGCCCAGACAAGT[G/T]GAGGGGAAGAGCTCT | 51317 |
rs562704588 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46088320 | TATCAGCAAGGCCAC[-/T]TTGCCTAGCCCAAAA | 51317 |
rs562758394 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45932625 | CAAATAGCACTTTTG[A/T]AATTTTTTTTTACAA | 51317 |
rs562765556 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930896 | AGCGTATGTCTCAGG[C/T]GGTCACAGGCCCCCC | 51317 |
rs562767599 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45938821 | AAACTTCAGATAAGG[G/T]GGAGACTAGTGTATT | 51317 |
rs562785427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45940553 | AAAAAGATAACATAT[A/G]TTCTAAAATATTACA | 51317 |
rs562808404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46066444 | TGTGGCTTGAACCTA[C/T]AATCCCAGTTACCTG | 51317 |
rs562813002 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46082660 | TCCCTTTTGAGTCAA[C/G]AAATGTAAATTTAAA | 51317 |
rs562815312 | snp | C/G | 0.000194571 | 0.00986143 | intron-variant | PHF21A | GRCh38.p7 | 11:46049361 | ATGCCCTCACCATTC[C/G]TTTTGATCCATTAGG | 51317 |
rs562852152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46091000 | CAAAGTAAAGAGCTA[C/T]AGGATCTTGATTATT | 51317 |
rs562855038 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46063377 | GATTGGCAAACTTTC[C/T]AAAAATAACCAGATA | 51317 |
rs562874798 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46015420 | AATTCTTTGCCTAGG[A/C]CAATTTCCAGAAAAG | 51317 |
rs562877994 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46023300 | ATGGCTAATTACTGA[G/T]GCCCCTTCTATTTTG | 51317 |
rs562893629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45974514 | GCTAGAGTGCAGTGG[C/T]GTAATCACAGCTCAC | 51317 |
rs562927195 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46079415 | AAATCTGGACAGAGA[A/C/T]GGGTGACAGTGGCTT | 51317 |
rs562937263 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45983971 | CATGACTGCTGCTGG[-/T]TCACTGACGAAGGTT | 51317 |
rs562938603 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46030774 | TAATTTGTAACTTTA[A/G]GAAGGTGACGATCAT | 51317 |
rs562962284 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46048071 | CACAGTTGCACAACT[A/C]CAGAATTAATTCCAG | 51317 |
rs562976712 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46107764 | AAGCTGGAATCAAGA[A/G]TTCTATTTAATGTAG | 51317 |
rs563013125 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45970621 | CTTGGGCACTGACAC[A/G]GTTAATTTGTGAGTT | 51317 |
rs563067641 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45990984 | ACAGCCACCATTATA[A/C]TATCACACAGAGTAG | 51317 |
rs563068611 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PHF21A | GRCh38.p7 | 11:46075224 | CTATGTTAGTTCTCA[C/T]AAACAAAAATTTCGA | 51317 |
rs563072755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46040363 | CAAAGAAAAATACTA[C/T]TTGGCACAGACAATA | 51317 |
rs563075203 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PHF21A | GRCh38.p7 | 11:45998739 | CTGGTCTCGAACTTC[A/G]GACCTCAAGTCATCC | 51317 |
rs563075263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45962112 | TGCCTGCTCCAAACA[C/T]ACTAGAAACTGAGTT | 51317 |
rs563087508 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45932779 | AAACAGTGCCCGAAC[A/G]ATGACACAAGGACTC | 51317 |
rs563107193 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45990293 | AAACAGGATCTCACT[A/C]TGTCCCCCAGGCTGG | 51317 |
rs563118412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46039279 | TGGAGAATTTGTTTC[A/G]ATTACTCAGCTTCAT | 51317 |
rs563162290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46044134 | GTTTCAACCTAAGCA[C/T]TACTGTTTAAATGAG | 51317 |
rs563163548 | snp | A/G | 0.00247689 | 0.0351043 | intron-variant | PHF21A | GRCh38.p7 | 11:46049385 | CATTAGGTTGAACCC[A/G]GCCCAAATACATACG | 51317 |
rs563169219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46031668 | TTTAGATTAATAGGC[A/G]CTCCGAGGCAGGTCA | 51317 |
rs563177292 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45961200 | GCTGGAATTTGCAAC[C/T]CCTGTTCTTTTTGGT | 51317 |
rs563186322 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46016490 | CTCTCATGCAACACC[G/T]TTCCTACCTGTCCAA | 51317 |
rs563245626 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46020994 | TGTATGATGGGTTTA[C/T]TGGACCATAACTCCA | 51317 |
rs563316218 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45977410 | CCAAAGTGTTGGGAT[G/T]ACAGGCGTGTGCCAC | 51317 |
rs563321465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45979124 | TGGGTTCAAGTGATT[C/T]TCCTGCCTCAGCCTG | 51317 |
rs563342742 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46035925 | AGAAGACACAGAGAG[G/T]TTTTAAGCAACCATT | 51317 |
rs563361093 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45935316 | GCGCTACACTCCCCC[C/G]ACACACTGTCAGGAA | 51317 |
rs563413977 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45975119 | AGGAGTTTGAGACCA[G/T]CCTTGGCAACATAGT | 51317 |
rs563420732 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46048039 | GAAGTGTAGAATTCA[A/G]TGGCTTTTAACATAT | 51317 |
rs563438457 | snp | A/G | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46119822 | TGACGAGAAGTGTTG[A/G]GAACTGCGTGCACGA | 51317 |
rs563452975 | snp | C/G/T | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45970913 | TGCACTGAATTTAGT[C/G/T]CTTGGTGTCAGGACG | 51317 |
rs563507956 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45995719 | TTAATACTGCAGACT[A/T]AAGCAGAAGCTGAAC | 51317 |
rs563509808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45986244 | CTAGCCTGATTGAAA[C/T]GCAGTTTTCTTATTT | 51317 |
rs563535448 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45941794 | TGCTTTGCTAGGCGC[A/T]GAGGACGTATGTTTT | 51317 |
rs563553259 | snp | C/G | 1.78376e-05 | 0.00298638 | intron-variant | PHF21A | GRCh38.p7 | 11:45969764 | AGAAAGAGCCCATGA[C/G]GATTTCTGTCCCATC | 51317 |
rs563582277 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46002691 | TTTGGACTCTGTCCC[A/C]GTAAAATGTCCTATG | 51317 |
rs563595964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46028060 | TAGTAGCTGATTCTC[C/T]AAATTCTTGAGTTGG | 51317 |
rs563622117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46018777 | AAAAATGATGATGCT[A/G]TACCAAGAATAACTG | 51317 |
rs563630179 | in-del | -/TC | | | intron-variant | PHF21A | GRCh38.p7 | 11:46115518 | AATGTTAACATATTA[-/TC]TCTTTTTTAAAAAAT | 51317 |
rs563630252 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46079588 | GATTTGGCAGGTCTA[C/T]TGGTTTGTTTCTTAC | 51317 |
rs563652785 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46103075 | CCGGCTGGACAGGGT[A/C]CTGCAGAGCTGAAAT | 51317 |
rs563661953 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930003 | CTGGAGAACCCAGGC[C/T]CTGGAAAATGCACCT | 51317 |
rs563676498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45950897 | CACAATGCTAACTCA[C/T]AGCTAAATGATTTTC | 51317 |
rs563676499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46120316 | GGGGTGGGGTGGGGG[A/G]GATGGAGGAGCCCCA | 51317 |
rs563721500 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46043366 | CACAGGTTACTTCTG[C/T]TTACCCACATCATCA | 51317 |
rs563728722 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45939908 | AAGGGAAGTGCTAGA[A/G]GTGACCCAGCAAGTC | 51317 |
rs563764945 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46086742 | ATTTTTCAAATATTC[A/G]TACTTCATTCTACTG | 51317 |
rs563779487 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PHF21A | GRCh38.p7 | 11:45934657 | TGGACTGAGCTCTCC[A/T]GGGTGGAAAACACAC | 51317 |
rs563795320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46112650 | AGTTAAAGCGTACAG[A/G]TATTCAAGATGTTGA | 51317 |
rs563807256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45961282 | GTATACTTTATATAC[C/T]TGTCTGCATGAAAAA | 51317 |
rs563814506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46010734 | ACAAGGAAAAAGATA[C/T]ATGTATTTCTGTGCC | 51317 |
rs563844861 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45943028 | TCTCATAACCTATAT[G/T]CAATCCTGATGGCTC | 51317 |
rs563855750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46076262 | CCGAAGTTTTTTCAC[A/G]TAATAGTAGGTCAAT | 51317 |
rs563873109 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46068390 | TACATATATATAATA[C/T]ATGCACATTATTTGA | 51317 |
rs563897316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45934501 | GAGTACTAACGCTTA[A/G]AAACAAACCGGCAGA | 51317 |
rs563898057 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45967825 | AAGAAATATATTTTA[C/T]TCTGTAATCAGCATG | 51317 |
rs563917036 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45964441 | TAAGGCAGCAGGCAG[-/C]CATCTGAACAGCCTC | 51317 |
rs563919406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46077217 | ACTACATGCTTTACA[A/G]CATTATCAACAAAGA | 51317 |
rs563921663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45977982 | ATTATGTAACCTCTC[C/T]GTGCCTTAGTTTTCT | 51317 |
rs563939443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45960444 | AAGCAGCCATAAGAG[A/G]TCACATATTGTATGA | 51317 |
rs563961413 | snp | C/T | 0.000200003 | 0.00999808 | missense, utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934045 | CCGGCGTGGAGGTGG[C/T]GGCATTGGCAGGGGG | 51317 |
rs564000766 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45959700 | CAAAGTTGTAGGGTA[C/G]AAGATCAAGACAAAA | 51317 |
rs564017360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46076975 | GTGGCCATAATACCA[C/T]CACCTAATGCACAGA | 51317 |
rs564032180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46069112 | ATATATACAACCTCT[C/T]GATCTTCAGAACTTT | 51317 |
rs564043656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46027940 | ATCTCATGCCAAAGG[A/G]AAGCAGCCAGCACCT | 51317 |
rs564051419 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:46016522 | CCTTACCCATTCTAG[-/A]AGACCTAGATCAAAC | 51317 |
rs564055980 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46013838 | GTAAAAATACACTAC[A/G]AAAGATGAAAAACGG | 51317 |
rs564059399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45976571 | GTAGTGCCAAGCGCA[A/G]TGGCTCATGTCTGTA | 51317 |
rs564080699 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46027039 | GAGCAGGAACACACA[C/T]GCACACATGCACGCA | 51317 |
rs564116879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46058742 | TCTGTACTAGTAATA[C/T]GGTCCCCTGGCTCAA | 51317 |
rs564118652 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45985226 | TTGATAAGTCACACC[A/C]ATATTCATCAACGCT | 51317 |
rs564149209 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46042803 | CCTTCTTGCTATGTC[C/G]TCACAGCAAGAAGGT | 51317 |
rs564163554 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46102004 | CGGGGATTACAGGCA[G/T]GTGCCACCACGCCCA | 51317 |
rs564176463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46070243 | ATTTAAAATTGAGAA[C/T]GATTCCATAAACGGC | 51317 |
rs564206074 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46081397 | TCTTCAATGAAAAAA[A/G]CTCTTGATTTTCCTT | 51317 |
rs564213475 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46078192 | TAAGTACGGGCTACC[A/G]ATGCCAGCTCTCAGA | 51317 |
rs564223646 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45941679 | CAGAGGAAGTCCTAC[A/G]GAGGCACCATACCAG | 51317 |
rs564230325 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46079416 | AATCTGGACAGAGAC[A/G]GGTGACAGTGGCTTC | 51317 |
rs564256970 | snp | C/T | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46102971 | GGGACGGAAAGAGAC[C/T]ATCAAGAGGGTAAGC | 51317 |
rs564266178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45994719 | TCAACTCTGTGCTGA[A/G]CTGGCAAAAGCTCTA | 51317 |
rs564266599 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46106162 | TCTGTTCCAAGTACA[A/G]CATGCTAACATTTTA | 51317 |
rs564332263 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45946507 | TCCTGCCTCAGCCTC[C/T]CACGTAGCTGGGACA | 51317 |
rs564365073 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45977360 | CAGGCTGGTCTCAAA[C/T]TCCTGACCTAAAGTG | 51317 |
rs564371975 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46035892 | GTTAAGATTTTGGAC[A/T]TGGTCCTAAGAGCAA | 51317 |
rs564374134 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46013673 | TACTTAAACAAACTT[A/C]GATGGTACAGCCTAC | 51317 |
rs564376961 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46050827 | AGTATGTCCAGCAAC[C/T]GAGTATGTGTGCAGG | 51317 |
rs564391528 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45966747 | GCCCCAGCCTCCTGA[A/G]TAGCTGGGGCTACAG | 51317 |
rs564402751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46067387 | TAAGTGACGTAGTAA[C/T]ATTGCAGAAGAGACT | 51317 |
rs564410360 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45986164 | AGGAGATGAGACCCT[G/T]TATTAATATCATTAG | 51317 |
rs564428048 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46001841 | GGGAAGAGGATGGAG[G/T]TCTTTGGTTTCTATG | 51317 |
rs564440420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46043563 | CTGAAGTGATAAAGA[C/T]GAGCTCTGCCAAACT | 51317 |
rs564461132 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46119485 | TCAACATATGACCGG[A/C]ATATGATGACACCAG | 51317 |
rs564484234 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46074031 | AAGGGAGAAACTGAG[-/T]TAAGTATCAAAGATT | 51317 |
rs564521217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46118647 | TGTATTTTTCAGACA[C/T]TTTTAATGACCCCCT | 51317 |
rs564535715 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45970333 | ACTCTCAGTATCTGG[C/T]TGAGTGACCTCGTTG | 51317 |
rs564544252 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46018203 | TGCAGTGAGCTGAGA[C/T]TGCGCCACTGCACTC | 51317 |
rs564591836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46056240 | TTTGTTTTCATTAAG[C/T]CTTTCTCAAGAGAGT | 51317 |
rs564595630 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46106487 | GAATTCTGCTCTGAG[A/G]TGTTGGGGGTTGGGG | 51317 |
rs564602894 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46017463 | TTTCTTGCTTTGGGT[A/G]TGTGGACTGATAACA | 51317 |
rs564647332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45949717 | TTGAGAGTTTAACAA[C/T]AGACAACACTTGTAA | 51317 |
rs564666555 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PHF21A | GRCh38.p7 | 11:45975352 | TAAAATAAAATAAAA[C/T]AAAATAAAATAAAAT | 51317 |
rs564680476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46055544 | CACAAATGCTAGCCA[C/T]AGGTTTCTTTCCATT | 51317 |
rs564685484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46007351 | GATGGAGTTTCACTC[C/T]TGTCCAGGCTGGGGT | 51317 |
rs564695341 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46092341 | AACAAAACACACACA[A/G]GTTTCCAAAGTTTTA | 51317 |
rs564711353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46021645 | CTCTTGGGCTCAAGC[A/G]ATCCTCCTGCCTCAG | 51317 |
rs564721398 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46056529 | ATAGGTCCTTGTAAA[C/T]GTCTTTCTAAAAGGG | 51317 |
rs564735568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45955116 | TATTTCCCCCTTTAT[A/G]CTAAACGCTATGTAA | 51317 |
rs564765094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46076209 | AAAGCAAGATGTTCT[C/T]CTCCTGCCCTATATA | 51317 |
rs564784138 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46053050 | AAGGGCCTCGAGTAA[C/T]GTGCCCCCTCCCAAA | 51317 |
rs564803490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45966983 | CTTTCCCCTTATGCA[C/T]GAAGCTTGACCTTCA | 51317 |
rs564825395 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46022410 | CAGTGAGCTGTGATC[A/C]CATCACTGCACTCCA | 51317 |
rs564863092 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46043890 | CATTTGGATGTGAGT[A/G]CAGAAAACAGTAAAA | 51317 |
rs564921665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46114755 | ATTTGTAAGTATGTC[A/G]CTTTGGAGATGCACA | 51317 |
rs564939368 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46006932 | GTCAGAACAACAGTC[A/G]GTAAAATTTAAAGAT | 51317 |
rs564956894 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45954623 | GTAGCTAGCATACTG[A/G]TAGACTGGGCTTGCA | 51317 |
rs564961302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46079515 | GAGTCCCAAACAAGG[C/T]CTGGAAAGAAGCTGG | 51317 |
rs564968643 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45997195 | TCTTCCTTTTTCCTA[G/T]GCTTGATGTATGAAA | 51317 |
rs565004961 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46003401 | ACCTATCCTCTCCCC[C/T]ACTGCTAAAAGAAAA | 51317 |
rs565037833 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46081017 | TTTGCTGTTTCAGAC[C/T]TGCTGTGTGGTACGC | 51317 |
rs565062088 | in-del | -/G | | | upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46122213 | CAACAGCAGTTTGAA[-/G]GGGGGGGGGGGAAAG | 51317 |
rs565068276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45972140 | TGCAATGAAACATGA[C/T]AAGGTGAAAACAAAC | 51317 |
rs565094988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46004964 | ACTTTTTCCCTTTAC[A/G]ATAATATTTGTCTCT | 51317 |
rs565125950 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PHF21A, LOC105376661 | GRCh38.p7 | 11:46123200 | CAGAACCAGAAATAG[C/T]CTTGGACTTTACTAG | 51317 |
rs565138264 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46122260 | CGAGGAGAAGTGATG[G/T]GGAAGCACTGCAATG | 51317 |
rs565148954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45963987 | GCAGGTCACTTGAGG[C/T]TGGGAGTTTGAGATC | 51317 |
rs565153983 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45940705 | AGAGGGTCAGCCTTT[A/C]TTGAACCTTATCCCT | 51317 |
rs565158186 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45954043 | CTCTCGTTGCCCAGG[A/C]TGGAGTGCAATGGCA | 51317 |
rs565167413 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45987576 | TGAGGCAGGAGAATT[A/G]CTTTAACCCAGGAGG | 51317 |
rs565168635 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46013887 | TGGTAGTTGTACTGG[C/G]TGAGTCAGTGAATGA | 51317 |
rs565176684 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46020309 | TTGGGGACAACACTA[C/G]AATTCCCTGAAGTGG | 51317 |
rs565188118 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46072142 | CTACAGATACAGATA[C/T]GCTACTGTAATAGAA | 51317 |
rs565212053 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45963061 | AAAGTAGGGAAAAAA[A/C]CAAATTACAAAATAC | 51317 |
rs565238062 | snp | C/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45929568 | TCTGGCCTGCCCGTC[C/G]CATCCCGCCTGACTG | 51317 |
rs565246493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46086861 | ATAACAAAGGGCTAA[C/T]ACAGTTTATATATTT | 51317 |
rs565296058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46013068 | TTCCTATATATTCAC[A/G]CCTATGATAAAGTTT | 51317 |
rs565298383 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46112757 | AACTATCCCCATTTT[A/T]AAAAAAAAGGAACAG | 51317 |
rs565303681 | snp | A/G | 0.000453176 | 0.015046 | downstream-variant-500B, utr-variant-3-prime, missense | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45928883 | ATCTTAGCATTGGGC[A/G]GACACCAGGGCAACC | 51317 |
rs565345669 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45944320 | TCCCCTAAAATAAGT[G/T]TGTATGGTAGGTGAG | 51317 |
rs565377498 | snp | C/T | | | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46118907 | GCTTAGAGTGAACAC[C/T]AGATGTAAACAAATA | 51317 |
rs565393680 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46097492 | TCCCTCAAATTATTG[A/G]GGAAATCTACAGCAG | 51317 |
rs565393782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46088531 | GGAAAGCACATTCAC[C/T]ATCCCAAAAAACAAA | 51317 |
rs565413408 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46037684 | TGCTTATCTGATTCT[A/T]ATCCTTTTGTAAGTA | 51317 |
rs565413862 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46105062 | TTACACATTAACTCA[C/G]TTATTCCTCATAACC | 51317 |
rs565414340 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46116500 | CATCACATCAATGGA[G/T]AAATGAAGAAAAACT | 51317 |
rs565420100 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45936152 | TCATGGTAGTACACA[A/C]CTATAGTCTCAGCTA | 51317 |
rs565457855 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46061359 | AGAACCTCAATGGTC[A/G]TTTAATAGGAATAGC | 51317 |
rs565465216 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45935985 | ATTTTCTTCCCCCAA[C/G]AAGTGCTACAGTCCA | 51317 |
rs565482212 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45952078 | CCAAAGTGGTGGGAT[G/T]ACAGGCGTGAGCCAC | 51317 |
rs565585922 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46051164 | CAAAAAGGATAACTT[C/T]CCACCTTTCAAGTTT | 51317 |
rs565601184 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46045322 | CACATTATTATACCA[C/G]GTACTAACACAAAGG | 51317 |
rs565605863 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46021011 | GGACCATAACTCCAT[C/T]ATACACTGAGGAGTA | 51317 |
rs565618364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46052965 | ACAAGATGAAGTAGA[A/G]GAATAATTCTCACAT | 51317 |
rs565620080 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46062097 | TTTTTGTTTTGTTTT[G/T]TTTTTTCCTCTAAGG | 51317 |
rs565620870 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45943945 | AAACGGAGAGGCATT[C/G]TACAGAAGAACTGGC | 51317 |
rs565641031 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46070487 | AGGTGCCCGCCACCA[A/C]ACCCAGCTAATTTTT | 51317 |
rs565655752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45997742 | CATTGTTGGGCCATC[C/T]GTTTATGTGTGCTGC | 51317 |
rs565672615 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46113149 | CAACTACAGGTCCCA[C/G]CATGCAGTGCTCTAA | 51317 |
rs565674319 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45951577 | TGTGGTTGCCAACTA[A/T]CTACATTCCTAATTT | 51317 |
rs565694983 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46079868 | GGAAAGGAAAGGAAA[C/G]GAAAGAGGAAAGGAA | 51317 |
rs565726962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46078593 | CTCTGTTAATTTTTC[C/T]GTTAGAAAGTAACAT | 51317 |
rs565748337 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45947472 | CCTCTCTGTATTAAA[C/T]TGGTGATGCCTATAG | 51317 |
rs565749607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46035282 | CCATCTTTCTCTACT[A/G]ATCTGAAATATTATC | 51317 |
rs565810243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45952212 | CAGTGATTCTGTCCA[A/G]CTAGAAGGTGAACTA | 51317 |
rs565814801 | snp | C/T | 1.67276e-05 | 0.00289197 | synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45935720 | CCATTTAAGTAACTT[C/T]TGTTTCTCTTCTTCT | 51317 |
rs565816999 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46044562 | TCTCTTACTCTTTCG[C/G]GCAACCCAGATTAGG | 51317 |
rs565832553 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46051706 | TGCCTCAACTCAAGG[A/G]GGTGAGGACACTGGT | 51317 |
rs565858503 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46121413 | CTCAGCAGCAGCAGC[C/G]AGCACCACCAGCCCA | 51317 |
rs565870107 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45961650 | CGACATGTTACATAG[A/C]AGTCTTTGTTGCAGG | 51317 |
rs565893551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46077714 | GATCACCCACACCTG[C/T]TGTCCAACAAGTTAC | 51317 |
rs565924332 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46027973 | CATTTTATTTGTCAG[C/T]AAGGAATTCATTTCA | 51317 |
rs565925317 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:45986550 | TGCATACTAGGAATG[G/T]TAGTTGTAATATATT | 51317 |
rs565926444 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46122473 | CGGGGGCCTTCGCTC[A/G]CCTTTATTTATTGCT | 51317 |
rs565960113 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46012558 | AGTCTCTGTTTATTC[A/T]CCTCTTAAATGGAGA | 51317 |
rs565970236 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46049789 | CACCCATTAGAGTCA[C/T]GAATAGCAAACTGCT | 51317 |
rs565983616 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46043166 | AGGTAAGAAATTCAA[C/T]CAATGTAAAGTACAC | 51317 |
rs566005562 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46056991 | TGCTTTAAATATAGT[-/A]AAAAAAAAAAGTCAA | 51317 |
rs566035958 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46094889 | TGGCGACAGAGTGAG[G/T]CTCCGTCCCAAAAAA | 51317 |
rs566049432 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46043807 | CCCACATTGAAATGA[A/G]TGCTCACTTTGGACT | 51317 |
rs566063500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45968204 | TGCCCACAGTCTTGA[C/T]CATCCCCAATTTATT | 51317 |
rs566064743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45976636 | CACTTGAGCTCCGGA[A/G]TTTGAGACCAGCCTG | 51317 |
rs566067603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46026703 | CTGTGGGCTTTTAAA[C/T]CCGTAATTAAAAAAC | 51317 |
rs566094138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45993255 | GTACTATTTTCCACA[A/G]ATATTTCCCTAATGA | 51317 |
rs566107636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45985587 | AGACAGGGAGGAATA[C/T]TGGTGGCAGAAGCTA | 51317 |
rs566112802 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45941599 | GAGAACTGCTGCCCA[C/T]AGAAATGAATATAAA | 51317 |
rs566125532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45969127 | AAAACTCCTTCTTCT[C/T]CTCCCTTTGTCTGAA | 51317 |
rs566155333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46031034 | GCCTACACCAGTGAG[C/T]GAACTTTTACAGGAA | 51317 |
rs566197379 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46109962 | CTCCAGCCTGGGCAA[C/G]AGGGCAAGACTCCGT | 51317 |
rs566228606 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46062074 | TCCCAATCCCTGTTT[A/G]CAACTGTTTTTTGTT | 51317 |
rs566230013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46111320 | ACTAAAAATATAACA[A/G]TTAGCCAGGCATGGA | 51317 |
rs566249952 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46059537 | TTCAAGCAATCCTCC[G/T]GACTCAGCTTCCCAA | 51317 |
rs566259090 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46007988 | GTACTTGGGATTACC[A/G]TGCTCCAGATAAGAA | 51317 |
rs566279169 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PHF21A | GRCh38.p7 | 11:46110853 | TGCAATGGCACAACC[A/G]CAGCTCACTGCAACC | 51317 |
rs566285048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45941209 | GCTCAGGTAATCCTC[C/T]CACCTCAGCCTCCCA | 51317 |
rs566286892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45949958 | AAAGAAGAGCTCCCC[C/T]AAATGAACAGAAGTC | 51317 |
rs566289953 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45933812 | ATCAATTGGCAAACT[C/T]TGGTGCCACCTGGCA | 51317 |
rs566304005 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45976568 | TTAGTAGTGCCAAGC[A/G]CAGTGGCTCATGTCT | 51317 |
rs566309959 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46119761 | AAAAAAAAAAAAAGA[A/T]ATCCTAACAGCACCG | 51317 |
rs566356474 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46102135 | TGCTGGGATTACAGG[C/T]GCGAGCCACCACGCC | 51317 |
rs566372115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45998763 | GTCATCCACCTACCT[C/T]GGCTTCCCAAAGTGC | 51317 |
rs566388451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46039658 | CAATTTTAGATCTAC[A/G]AAGGCTGAATTAAGT | 51317 |
rs566388817 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46000453 | CTAAAGACAAGTACA[C/T]AATTACCAGAAACTA | 51317 |
rs566389011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45982080 | TGTCACCTCAACCTA[C/T]CAAGTAGCTGGGACT | 51317 |
rs566405525 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45941828 | GAAGCACTCTGGCAA[A/T]ACCAACTGCAATTTC | 51317 |
rs566414089 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PHF21A | GRCh38.p7 | 11:46051119 | TTAGTCTCTCTGAGG[C/T]AAAATACACCACATT | 51317 |
rs566418297 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46081833 | CATTTATATATTGTC[C/T]GTGGCTGTTTTCTCT | 51317 |
rs566426258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46091272 | AGTCTTGCACTAGGC[A/G]ACTACCCTATTCCAG | 51317 |
rs566446846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45982689 | GCTTCAGTCCTCCTC[C/T]CCATCAGACATCAAA | 51317 |
rs566456990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45973241 | GACAGTGGAGATAGA[C/T]GGTATTTCCAACATC | 51317 |
rs566512225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46099996 | CTATCCTTAATGAAC[A/G]TTTATCTTTTTATCA | 51317 |
rs566539044 | in-del | -/A | 0.00835141 | 0.0640778 | intron-variant | PHF21A | GRCh38.p7 | 11:46107738 | TCTCAGCAACAAGTT[-/A]AAAACTCTCAAAGCT | 51317 |
rs566550183 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46115884 | TGTCTTCACAGAAAG[C/G]TTTACTATTCACTGT | 51317 |
rs566580331 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46004851 | TCCCATTCACTACAC[A/G]CATACTTACATGTGT | 51317 |
rs566588040 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:46017342 | GAAAAAATCAGATTT[-/G]TTTTTTTAGCACTCA | 51317 |
rs566588240 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45961699 | AGAAACATAATTCCT[C/G]AGAACTCCATCAAGC | 51317 |
rs566593175 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45973814 | CAATCCAGTGCTATC[A/G]TGGATTGTGGGAGTA | 51317 |
rs566598645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46023015 | CTTGGCCTCCCAAAG[C/T]GCTGAGATTATGGGC | 51317 |
rs566631624 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45994086 | ATGATATACTTCCTC[A/G]TCTACATAGTATGAT | 51317 |
rs566643922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46046410 | AAGAGAAACCAAAAA[C/T]TAAAACAAACCAAAC | 51317 |
rs566671194 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45990643 | TCCAGTTTCTACATA[A/C]AGCAAAAGTATTGAC | 51317 |
rs566674592 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46087074 | TGTCAGGTGCCACTT[C/T]GCAATTTGCTGATGG | 51317 |
rs566701845 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46047624 | ATTAAGAGTCTGAAA[C/G]ATATTATTTTTTCTT | 51317 |
rs566718529 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46014161 | CAACCCTTGCTCCCA[A/T]CCTTCCCTACTCACT | 51317 |
rs566750621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46099014 | TAAGAAAGGTCAATG[C/T]TAGATACCAGATTTT | 51317 |
rs566755078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46021964 | CAGGCATTGCACTAG[C/T]AGGAAAGGAAAAGAT | 51317 |
rs566768684 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45978467 | TCTTTAGTGTTCTTA[C/T]AAAAAATTCATTCTT | 51317 |
rs566810785 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46011918 | TAAAACATTAGGCAC[A/G]AAAATTAGAAGCAAC | 51317 |
rs566816207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45938373 | AATTTTAATGTTAAC[A/G]TGCACATTCTAGATG | 51317 |
rs566844256 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45971625 | AGTAATAACTGCAGA[A/C]TAATTCAGGCACAGG | 51317 |
rs566860788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46072309 | AAGTTCAGGCCCATG[A/G]GATCTAACTGGAAGT | 51317 |
rs566867887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46013597 | GTTGCTTAATAACAG[A/G]GATATGTCCTGAGAA | 51317 |
rs566889209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45954385 | ACATACACAGTCTCC[C/T]ATTTCGGAACAATTC | 51317 |
rs566890113 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46096242 | ATCAATTTTCCCCTC[A/T]TCATTACTGGATCAT | 51317 |
rs566900868 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45952094 | ACAGGCGTGAGCCAC[C/T]GCGCCCAGCCTAAAT | 51317 |
rs566901321 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PHF21A | GRCh38.p7 | 11:46055468 | GGCATTCAGAATGAG[A/G]AGTGACAATTAAACC | 51317 |
rs566922604 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46055185 | CTGGACATTAATAAT[G/T]TATCCCATTCTGTTA | 51317 |
rs566937128 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45983967 | GACGTCATGACTGCT[A/G]CTGGTCACTGACGAA | 51317 |
rs566942448 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46033501 | ACTCCTGGGCTCAAG[A/C]AATCCACCGGCCTCA | 51317 |
rs566944636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46115051 | AAACATTTCTGTAAC[C/T]GATTCCAAAGTATAG | 51317 |
rs566950476 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46021246 | TTTTATTTTTTGTAG[A/T]GATGGGGGTCTCACT | 51317 |
rs566971951 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45929658 | CTGGGGAAGGGGTAG[C/G]GGGGTGGGGTCCTCA | 51317 |
rs566972888 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46063372 | AGTAAGATTGGCAAA[C/G]TTTCTAAAAATAACC | 51317 |
rs566981581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45988495 | ATTGGGAAGTATTTT[C/T]AACAAAAGTACATTC | 51317 |
rs566996207 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45959893 | CAAAGGATTTGAATA[G/T]ACCTTTTTCCATGGA | 51317 |
rs567004952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46088814 | GTAGGCTTTTCTGTT[C/T]TCAAATTCTCTAAGG | 51317 |
rs567016485 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46092530 | CTCATTTAAATAACA[C/T]ACAACTACTCCTTCA | 51317 |
rs567029604 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46093359 | AGCTTCATGTCTCCC[-/A]GATTGTAAATCTTTG | 51317 |
rs567069646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46089284 | AAATACTTCCTACTA[C/T]GTATCTAATATGTAG | 51317 |
rs567093126 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46038095 | CCTCCCTGTATTGAG[C/T]TTACTTGTATACTCC | 51317 |
rs567154493 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930505 | GGAAGAAATCAAAAC[C/T]CCAGAGGAGCTCAGC | 51317 |
rs567161195 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:46030144 | CTGCTGACTCTATCT[A/G]GAGAATATCTTGCTA | 51317 |
rs567172067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46079742 | GGAACAATACAAAAC[C/T]CTATCTAACTCGATT | 51317 |
rs567175404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46046288 | TAGCACTGGGGCCAT[C/T]CTCCTATGGGGCAGC | 51317 |
rs567206877 | snp | A/G/T | 0.00716625 | 0.0594738 | intron-variant | PHF21A | GRCh38.p7 | 11:46089580 | GCAACCCTGATTTTC[A/G/T]AGGCGAACCCTCTGA | 51317 |
rs567259366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45990529 | CCTCCCAAAGTGCTG[A/G]GATTACAGGTGTGTG | 51317 |
rs567289784 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46021316 | ATCCTCCTGCCTTGG[C/G]CTTCCAAAGTGCTGG | 51317 |
rs567294978 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46098263 | TGGGTGTAGTAAACA[A/C]TGATTATCTATTACT | 51317 |
rs567296234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45989390 | CCAGACGCGGTGGCT[C/T]ATGCCTATAATCCCA | 51317 |
rs567301590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46007039 | CGTTCCTGCAAGCTC[A/G]TTTTACAGGTGATTT | 51317 |
rs567305178 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45990508 | CAAGCGATCCACCCG[C/T]CTCAGCCTCCCAAAG | 51317 |
rs567312812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46107024 | GCTGTCCCCACGGCT[A/G]CCTCTTCTGCAGGAA | 51317 |
rs567327179 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46020472 | GGAAGTGCTTACCAG[C/G]CTTGTGGATTACTGC | 51317 |
rs567348258 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46034306 | TGTAAGACTAATAAC[C/T]CTTTGTCACACATGT | 51317 |
rs567361493 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45979072 | CCCAGGCTGGAGTGC[A/C]GTGGTGTGATCTCAG | 51317 |
rs567379035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45972556 | ACCGAGGCAGGTGGA[C/T]CGTCTGAGGTCAGGA | 51317 |
rs567381112 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46030357 | CAAGACGATCCTGCA[A/C/T]GATCTTTTATTCTTA | 51317 |
rs567397243 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930940 | AGGTCTGAGGGGACA[G/T]TGAAGGACAGGGAGA | 51317 |
rs567398668 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46013491 | CGTGAGTAACTAAAG[A/C]CACAGAAATGGAAAC | 51317 |
rs567417248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45937552 | GTGGTGTGACCTCCG[C/T]TCACTGCAGCCTCCA | 51317 |
rs567436779 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46114854 | TACTGACAGTTTGTA[C/T]TCTCAATGCAGCCAA | 51317 |
rs567440345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46054252 | AGTCAGAGTATTAAT[A/G]TGATAGTAACCCTTG | 51317 |
rs567462704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45998732 | GGTCAGGCTGGTCTC[A/G]AACTTCGGACCTCAA | 51317 |
rs567474187 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46114193 | CTCTCATCCACTGAC[C/G]TCTTCTGAAAACACA | 51317 |
rs567482049 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:45987778 | GAGCAAAACGTCTGT[C/G]CCTCTGTAACTGTCT | 51317 |
rs567497572 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46055126 | ACTTTTAAATTATGG[C/T]GAGAACTTAAGATAC | 51317 |
rs567500533 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PHF21A | GRCh38.p7 | 11:45984211 | AAGACGGAAGGGAGA[A/G]AGGGAGAAAAAATTA | 51317 |
rs567511527 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46018550 | CTATCCTGAAATAGC[A/C/T]GTCTGTGCATAATTT | 51317 |
rs567540000 | in-del | -/A | 0.00716266 | 0.059414 | intron-variant | PHF21A | GRCh38.p7 | 11:46035423 | GTATGTTTTGACTCT[-/A]GTTGGTTACTTCATT | 51317 |
rs567558363 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46029399 | AAGGATTAAAAAATT[A/C]TTCACTGGCTGGGCG | 51317 |
rs567564660 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45955042 | TATCAATACTGTGGC[A/G]ACCAGTGCTCTGGGG | 51317 |
rs567570681 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45987020 | ATCTAGGTACATCCC[A/G]GATTTCTTATACCTC | 51317 |
rs567586189 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46088785 | TTCTCTACATAGTAT[A/C]TATCTAGAAGACTGT | 51317 |
rs567643583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45961846 | GTCTTCTGGCTTCAT[C/T]TACTTTTCTGTCTAA | 51317 |
rs567675446 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46058153 | CACCTCCCTACATTC[-/T]TACTGCTGCCTTACC | 51317 |
rs567682452 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46017619 | CATCTCCTCAAAAAA[A/T]CCAAACTGGAAAAGA | 51317 |
rs567690245 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45970373 | GGATTCCTGGATAAG[C/T]GGTGAACCTTCACTT | 51317 |
rs567698165 | snp | C/T | 2.48154e-05 | 0.00352237 | intron-variant | PHF21A | GRCh38.p7 | 11:46079091 | TTTTATTTTAAATTA[C/T]TTTTAAATTTAACAA | 51317 |
rs567723415 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46016964 | TTACTAAAAATGTTT[A/C]ACCTGGATTTTTTTT | 51317 |
rs567743845 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46015013 | AAATAAAAAAATAAA[A/T]AAAAATAAAAAAATA | 51317 |
rs567812324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45996305 | AGGTAGTAAAGCTTA[C/T]AGGTTGACACATTAT | 51317 |
rs567817855 | snp | A/G | | | upstream-variant-2KB | PHF21A, LOC105376661 | GRCh38.p7 | 11:46123248 | AATAATATTTCTATT[A/G]CCTTGTTATGTATTT | 51317 |
rs567820596 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46055176 | AGAATCCTTCTGGAC[A/G]TTAATAATTTATCCC | 51317 |
rs567851115 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | PHF21A | GRCh38.p7 | 11:45944877 | GTTCCAGGGATTCTC[C/T]TGCCTCAGCCTCCAG | 51317 |
rs567855106 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46037776 | AACTTGAACAATACT[G/T]GAAAATTTTAGCAAC | 51317 |
rs567891716 | in-del | -/C | 0.394538 | 0.203982 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930905 | TCAGGTGGTCACAGG[-/C]CCCCCCCCCCTCCCC | 51317 |
rs567942197 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46028613 | GAGTCTCGTTCTGTC[A/G]CCCAGGCTGGAGTGC | 51317 |
rs567948509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45978388 | TAGGGTGAGGAGTAT[A/G]TCCATTATGTAAAAC | 51317 |
rs567957978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46100768 | CAGAAATAAGTCTAC[C/T]ATTACCTTGTAGTGA | 51317 |
rs567961643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45958059 | CACACATTACCAAAA[C/T]TGACTCAAGATAAAG | 51317 |
rs567962108 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45982940 | GAAAGGGTGTTTTTT[C/T]CTCCTCTACAGCCAT | 51317 |
rs567997648 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45973242 | ACAGTGGAGATAGAC[A/G]GTATTTCCAACATCA | 51317 |
rs567998144 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45928995 | CCCCTTGCTGCTATT[G/T]TATGGCTGGGGACTG | 51317 |
rs567998784 | snp | A/T | | | synonymous-codon, missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934145 | GCCGTGGATGAGGCG[A/T]ATCAGCTGTTTTACC | 51317 |
rs568024778 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46118917 | AACACCAGATGTAAA[A/C]AAATATCATAAACAC | 51317 |
rs568027178 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46059079 | AGTTAGATTCTACTA[C/T]ACATACCAAAGAAAG | 51317 |
rs568049557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46025500 | ACATTTTCTTAATCA[C/T]GTATAGCTCTGGACT | 51317 |
rs568081507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46108226 | TGCTCTCTTTATAAG[C/T]AGCTACTAGAATAAA | 51317 |
rs568090324 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46002557 | ACACATGGCCTTTTT[A/C/T]ATTTAAGGGCAGAAA | 51317 |
rs568090676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46074804 | CACCGTGCCTGGCCA[A/G]TAAAACTATTCTAAA | 51317 |
rs568106137 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45947868 | CTTAGGGTTTCCCAT[A/C]TAAATATTTTTGAGT | 51317 |
rs568132453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46107891 | TACTGAGTTATCAGC[A/G]TAGCATTTGGTAGTG | 51317 |
rs568195107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46109302 | CTGTGAGGATTAAAA[C/T]TAAATAAGATCCTAT | 51317 |
rs568224306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45966705 | GCTCACAGCAGCCTC[C/T]GCCTCCCAGGTTCAA | 51317 |
rs568248561 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45932954 | GTAAAATAAAACTTT[C/T]CTTAAAGAAAAAAAG | 51317 |
rs568252940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46024566 | GGACTTTGGGAGGCC[A/G]AGGCAGGTGGATCAC | 51317 |
rs568272947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45992255 | GAAAATTTTTCAGCC[C/T]GGCATGGTGGCTCAT | 51317 |
rs568289589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46032553 | ATCTTTATTCACTTA[C/T]CTGAATCCTTCCTGA | 51317 |
rs568314035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46083073 | CAAACTGGGTATTCA[A/G]CACACCTCTATGTTA | 51317 |
rs568314059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46073200 | AGGCGTGGTGGCGGG[C/T]GCCTGTAGTCCCAGC | 51317 |
rs568359713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46092597 | ATTAACAAATTAAGG[C/T]AACATCACTAGTTCT | 51317 |
rs568368666 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45946866 | CAAAATTCAAGTTAA[C/T]TATTCTTATCCCTTG | 51317 |
rs568408725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46116953 | GCCTGGGAAACAGAG[C/T]GAGACTCCGTCTCAA | 51317 |
rs568425169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46117542 | TCTATATTAGAATCA[C/T]AGTCTGTAAATCCGA | 51317 |
rs568430068 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45955659 | AAAAGTACAATTATC[G/T]CAGTGTTATATAAAT | 51317 |
rs568430611 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45931898 | TGGTTTTCTCAAGGA[A/G]AGGCCACAACCGGCC | 51317 |
rs568489438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45939304 | TTCACAATATGATAC[A/G]AACAATTCTCATCAC | 51317 |
rs568505188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46008622 | GTGGAAATGTGACTC[A/G]GTTTTGTGTATGAAA | 51317 |
rs568517508 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46040711 | GAAACTGCATACTAT[G/T]TTGGAGAGCAAAGGA | 51317 |
rs568550353 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45961429 | ACTATTGCACCAGTA[C/T]TAAAATGGGGTAAGG | 51317 |
rs568555988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46001218 | CATGTATGGTTCTGG[C/T]AGAGAATCTGAAGGG | 51317 |
rs568566614 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46022950 | GAGATAGGGTTTCGC[A/C]ATCTTGGCCAGGCTG | 51317 |
rs568573645 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45937471 | AAAGTGAAATGGGTG[C/T]TGTTTTATTATTAGT | 51317 |
rs568590254 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45959969 | AGTCATTAGGGAAAT[-/G]CACATCAACACTACT | 51317 |
rs568606618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46048713 | AGGCAGAGGCTGCAG[A/G]GAGTCAAGATGGCGC | 51317 |
rs568608984 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46023306 | AATTACTGAGGCCCC[G/T]TCTATTTTGAACATT | 51317 |
rs568626154 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46068789 | GTCATTCCATTTGCC[A/G]GCACCAAAAATACGT | 51317 |
rs568646700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46015837 | CTTCTATGGTAACAA[C/T]GCCTTCGTCTGAAAT | 51317 |
rs568671332 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45991277 | GTAGTACCTTGATTT[C/T]TTCCATATGGTCTAA | 51317 |
rs568746067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46007757 | GAAGTGAGATGTGTA[C/T]CCTTTACATAACCTA | 51317 |
rs568787726 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46046445 | ACCAAAAAACCTTGC[C/G]ATGACAGCCTCAACA | 51317 |
rs568792162 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46076746 | GCCCCCCTCCCCTTT[C/T]CCCCTACCTGTTTCT | 51317 |
rs568798541 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45964135 | CCTGGGAGGCGGAGG[C/T]TGCAGTGAGCTGAGA | 51317 |
rs568801452 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46100912 | AGCAGGTAGTCAAAA[C/G]TCCCTCCTTGACAAA | 51317 |
rs568814206 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:45974855 | TTCTCCACAGTTTCA[A/T]GATGGGGTCCTTTAT | 51317 |
rs568828878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46066945 | ATACTGAATTATACC[A/G]TATGTCTGTTTTACA | 51317 |
rs568830188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46074077 | AATAAGAACTAGTGT[C/T]TACCGCAAGAAATAG | 51317 |
rs568833537 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45998638 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 51317 |
rs568835928 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45961927 | GAGCCACAGTGTAAC[A/G]TGGTTTCTAATAAGG | 51317 |
rs568847499 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45965954 | ATAGCCTTAACTCGC[A/T]TTTGAAATTTCTTCA | 51317 |
rs568855055 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46032433 | TGTGAAAATCAGTAT[A/C]ATCTACTTCCTTTTC | 51317 |
rs568870108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46084109 | AGAGATGGACTTGTT[C/T]ACTAATCTTAGCCAT | 51317 |
rs568907924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46091937 | TTGGAAAACGGGACT[C/T]TTACATTTTAACAGG | 51317 |
rs568976064 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46116835 | GGGCGTAGTGGCGGA[C/G]ACCTCTATAATCACA | 51317 |
rs568991669 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45966681 | CTGGAGTGCAGTGGC[A/G]CGACCTCGGCTCACA | 51317 |
rs568998959 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45982132 | CAGCTAATTTTTTTA[A/T]TTTTTGTAGAGATGG | 51317 |
rs569003560 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46108118 | GGTTTGCCCCAATTC[C/T]TGCCTATTTACTTTG | 51317 |
rs569005591 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930736 | GGGCCCAGTGGGCAG[A/C]CGCTCCAGCTCTCTG | 51317 |
rs569048710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46031942 | TGGGCCACACAGTTA[C/T]CCAATTTTCCCCAAT | 51317 |
rs569073969 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45931109 | GAATCCACAGCCCAG[C/G]TGCAGGCGAGGTCAG | 51317 |
rs569090981 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46041377 | TTGGGCACTGTGCGT[A/T]CTTCTTTCGAGCAAT | 51317 |
rs569103682 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46084881 | GAGACGGGGTTTCAC[A/C]GTGTTAGCCAGGATG | 51317 |
rs569104119 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46080677 | TCTTTTTTTGTTTTT[G/T]GTTTTTTAAAGATGG | 51317 |
rs569115421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46062405 | ATCCCCCTTTGTCTC[C/T]TCCATCTATTTATTG | 51317 |
rs569156248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46100621 | ATGCCAAATAACATC[A/G]TAACATTAAAGACAC | 51317 |
rs569161626 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45964620 | TTCTTCTTTCTCATC[A/C]CTAGTCGTTTTTCAA | 51317 |
rs569163470 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45954507 | TAAGAGTGGGCCATC[C/T]TGCAAGAGGCTGACT | 51317 |
rs569202982 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45959439 | TTTATGAAAACACAG[C/T]TAACATCATACTCAA | 51317 |
rs569212714 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45931765 | GTACAGAGCCTCCAC[C/T]GCCCTCCCATCGGCC | 51317 |
rs569217039 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46081609 | AGGGGTAGGACAGGA[C/T]GAGCTGGCCAACTTA | 51317 |
rs569228270 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45963540 | CTCTCTTTAGATTAC[C/G]GGGAAAAGCACCTTC | 51317 |
rs569244595 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46060823 | AGCTCTTTAGTTTAT[C/T]TGGATCCCATTTGTC | 51317 |
rs569278923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46112299 | TCTGATCAAATTATA[C/T]TGTAAAAAGAGAGGA | 51317 |
rs569300335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45947695 | CAGATACTGCCCACT[A/G]TCAGGCCAATTATTG | 51317 |
rs569313792 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45942723 | CAAAGGTAACACTTT[C/G]TTTGTTACCTCTGGA | 51317 |
rs569320775 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45956630 | TTGTTAAAAACGTAT[G/T]AATGTTTACTGTAAT | 51317 |
rs569320861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46008530 | GGTCAAAGGTAGAAG[A/G]CGGGAAAAGAGTCTG | 51317 |
rs569329475 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46047676 | TGACAAGAAGGCAGT[G/T]ACTAACAACCAGAAA | 51317 |
rs569330635 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45972461 | CTGATTTGGCAGCCA[C/G]TAGCCACAAGTTGCT | 51317 |
rs569356034 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46028141 | ACAACAAAAAAAGAA[C/T]TGAAAAAGTTGTGCA | 51317 |
rs569377852 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46065431 | GCAGTGGTTGCCGAC[A/G]TGCTGAGCATGGCAG | 51317 |
rs569379551 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | PHF21A | GRCh38.p7 | 11:46007310 | CCATCTACCTTTTTT[A/C]TTCTTCTTCTTTTTT | 51317 |
rs569396624 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45986230 | AGACCTTTTATTTGC[A/T]AGCCTGATTGAAATG | 51317 |
rs569399883 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46062238 | ATTAATCTGGAATTA[C/T]ATGCCCTTCGGTTGT | 51317 |
rs569419187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46055885 | AAATTGAATAGTTTT[A/G]TTTTGCTAATTCAGA | 51317 |
rs569421546 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46073164 | AAACCCGGTCTCTAC[C/T]AAAAATACAAAAAAT | 51317 |
rs569478204 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46097132 | TTCACCTAGATAATT[G/T]CAACAGCCTCCTAAC | 51317 |
rs569512762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46076477 | TTACCCCATCCCCTA[C/T]AGGTAAACTATAGAG | 51317 |
rs569531843 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46122385 | CCACCCCGCCCCCTT[C/T]CCAAATAACTACCCT | 51317 |
rs569532229 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45957721 | CCTAACTTTACACCT[A/T]AAGAAACAGAAAAAG | 51317 |
rs569547267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46086085 | TTAGAAAGGGAGACA[C/T]ACTATGGTGAACAAA | 51317 |
rs569551924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45973026 | GAGGCTGCAGTGAGC[C/T]GAGATCACACCATTG | 51317 |
rs569565678 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45960882 | TGGCAACTTTTAAAA[A/C]CATCTGGATTTCAGG | 51317 |
rs569586502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46004262 | AAACCAAATAACTCA[A/G]TGCAAAAGAGCTCTT | 51317 |
rs569602100 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46030828 | GTGTGTGCGTGTGTG[C/T]GCGTGTGTGTGTGTG | 51317 |
rs569618859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46060538 | AAATTCTAACCACTC[A/G]TTGTGGTTCTGATGT | 51317 |
rs569629327 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45960102 | AAAATGATTTAGCTG[C/G]TGTGGAAAACAGTTT | 51317 |
rs569678009 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46121238 | CTTCCCCAGGCAAGG[G/T]GGGGTGGGGAGGAGG | 51317 |
rs569681257 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46109525 | AATAAAATTTATATA[A/G]TTAGTAAAATAAAAT | 51317 |
rs569681294 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46072316 | GGCCCATGGGATCTA[A/T]CTGGAAGTGGTGCAT | 51317 |
rs569698305 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | PHF21A | GRCh38.p7 | 11:45934902 | ATGCCATGGGTAGGT[A/G]TGGTGAGGAGGAGAA | 51317 |
rs569717176 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45942642 | TCTGTAACCACCAGC[A/G]ACGTCTAAGGAAGGA | 51317 |
rs569717937 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45933642 | ACAGAAACAAACCCA[C/T]CGTGGCTGTGGAGGC | 51317 |
rs569727040 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46053129 | ATTCAAAATTTGTAA[G/T]TAAATGTAATGTGTA | 51317 |
rs569737461 | in-del | -/TA | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45931003 | CAGTGTTTTGGAATT[-/TA]TGAGTGCAGAATGTA | 51317 |
rs569750101 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45938593 | ACTGAACCCTATAAA[C/T]ATGTTTTTCTATACA | 51317 |
rs569774370 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45945630 | GGCTGAGTTCCATGA[-/G]GGTTATATTTAACAT | 51317 |
rs569808501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45968115 | GTAAAGTGCCTAGCA[C/T]AGTACCTAGTATGTA | 51317 |
rs569813239 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46052247 | GCTGTAAACCTAGAG[C/T]TGCCAGAGGCAACCT | 51317 |
rs569828064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46011275 | GGGCAGATCACCTGA[A/G]GTCAGGAGTTCAAGG | 51317 |
rs569833544 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46018660 | ATATGTCACATGACT[A/T]GGCAAAAGATAATTT | 51317 |
rs569834687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46085230 | GATATTTTAAAATGT[A/G]TCTATCGTGTGTAAT | 51317 |
rs569868867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46026646 | ATGCAAAAAAAAAAT[C/T]CTTTAAAGTCAAGCA | 51317 |
rs569872613 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46117228 | AGCAGATTTATCAAA[C/G]TTTCTAGCATCCCCA | 51317 |
rs569872620 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46080594 | GTGTTAAAGTTCTTA[A/C]ATCCACATTGTAGTT | 51317 |
rs569897811 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46057836 | TGCCAAGTGTAAAAA[C/T]ATGGTGCTTAAGGGA | 51317 |
rs569908376 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46092995 | CCTGGGCTCAAGCAA[A/T]CCTCCCTGCCTCAAC | 51317 |
rs569926349 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46017583 | TTGCCCTTAAGGGGG[A/G]AAAAAAAAAAACACC | 51317 |
rs569943954 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46019041 | CAAGAAAAAGAAAGG[A/G]GGAAGAAAATAAGCC | 51317 |
rs569967615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46042468 | CGTTATAAGACTGGA[C/T]TAAAATCACTGAATG | 51317 |
rs569991990 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46102072 | CATGTTGGCCAGGAT[C/G]GTCTCAAACTCCTGA | 51317 |
rs570059505 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46049690 | TGACAAAGAGCAGCC[A/G]CTGTCCTACTCAGGG | 51317 |
rs570083204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46034216 | GCCTTAATATTAGTG[C/T]CCCCACCCCCCCCTT | 51317 |
rs570110422 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46111235 | GCACTTTGGGAGGCC[A/G]AGGTGGGCAGATCAC | 51317 |
rs570125052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46001407 | TGTACTTAGCCAATG[C/T]ACCTGTAGATTCTAA | 51317 |
rs570137680 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45949046 | TGACTGTCAACATGC[C/G]GACTAGTTAGTGCTA | 51317 |
rs570162407 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46042832 | GTGCTATCTATGAAG[C/G]AGACAGTAGGTCCTC | 51317 |
rs570176017 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46120753 | CCCCCTACCTCCCCC[A/C]ACAACAAACTCCAAG | 51317 |
rs570186479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45985256 | TGAGGATGCAGGAAG[A/G]AGACAGGGCAGTCTT | 51317 |
rs570194241 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46002877 | AAACAAAAAAACACC[C/G]AATGTATTTAACATT | 51317 |
rs570213524 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:46067615 | AAAAAAAAAAAAACT[A/G]AATTGAATCATTTAA | 51317 |
rs570233558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46109622 | TTTATAATATACACA[C/T]AAATGTACCAATGTG | 51317 |
rs570243131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46118760 | AATTAAAATGAATAA[C/T]AGTATTTCCAGTAAA | 51317 |
rs570255990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45958617 | TCTCCAAAAAATAAC[A/G]AAAAAAATTAAATTA | 51317 |
rs570277668 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:45940341 | GCTGGGATTACAGGC[A/G]CCCACCACCACGCCT | 51317 |
rs570345993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46110613 | TTATATTTAGCCCTT[C/T]GTATTAACTCCTTTG | 51317 |
rs570352857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45949335 | CAGGTTTTCAGAGGG[A/G]AGGCACTGAACAGCT | 51317 |
rs570353123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46092846 | CACTGCAGCCTCAAC[C/T]TCCCAGGCTCAAGCA | 51317 |
rs570360276 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46003341 | TGTGTCTAGTCATCA[C/T]TCAGACTCTCTTCGG | 51317 |
rs570373317 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:45968034 | CTAAACCTTAGATTC[C/T]TTACCCTAAAAAGAG | 51317 |
rs570406346 | in-del | -/C | 0.00597247 | 0.0543191 | intron-variant | PHF21A | GRCh38.p7 | 11:46059576 | ACTACACACATGCCA[-/C]CCACACCTGGCTAAC | 51317 |
rs570419148 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46051417 | GAGCATTTACCATTA[A/C]CTCCCACCTCCATTC | 51317 |
rs570423930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45959874 | AACCCAATTTAAAAA[C/T]TGGCAAAGGATTTGA | 51317 |
rs570429036 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46085928 | TAACATCAAAATACT[A/C]AAACCTAAAAAAGAA | 51317 |
rs570433534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45967298 | GCTTGAACCTGGGAC[A/G]TGGAGGTTGCAGTGA | 51317 |
rs570452880 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46068727 | CCAGTGTCAACATAT[A/G]TAACACCTGATGACA | 51317 |
rs570456532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46076448 | TCTCTATCACCTATT[C/T]TCACTAACTGCCTTT | 51317 |
rs570506298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46085124 | ATGGGGAAATTCTGG[C/T]ATAACTTAAACATTT | 51317 |
rs570513181 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46060454 | ACTCATATAAAATTA[C/T]GTTATATTATATAAA | 51317 |
rs570528497 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46060433 | CAAGTTGTAATCTTA[C/G]CACATACTCATATAA | 51317 |
rs570534639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45941942 | CAGAGGATTAGTGTC[C/T]GGTAGGTTTTGTATT | 51317 |
rs570567371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46059656 | TCTCAAACTGGCCTC[A/G]AAGGATCCTTCTGCC | 51317 |
rs570588523 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PHF21A | GRCh38.p7 | 11:46101487 | AGGTACGTGGGGTTA[C/T]ATTATTCACTCTATT | 51317 |
rs570594875 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45933607 | CTCCCTCCGCCCGTC[C/T]CTGCTCCCCACCCAA | 51317 |
rs570614603 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45959039 | AAACTGAATCCAAGA[C/G]CATATTAAAAGGATG | 51317 |
rs570654769 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46017741 | TAAAAACTGTTCTTG[A/C]TAAATATGTAGACTG | 51317 |
rs570658680 | snp | C/T | | | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46119360 | GCCCGGACCTTCACT[C/T]AGATTTGAAATTCTA | 51317 |
rs570659764 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PHF21A | GRCh38.p7 | 11:45933143 | CTTCCTGGACACACA[C/T]ATCCTTCTTCCCTGC | 51317 |
rs570662024 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46110687 | ACAAATTGATGTCAT[A/G]TAAATAAAACAGCTT | 51317 |
rs570671017 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46075886 | CAACATAAAAATCAG[C/T]TATTGAGAACTATTT | 51317 |
rs570702945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46065718 | GCCAGGACTAGAATT[C/T]ACTCCTTTTCTTTAA | 51317 |
rs570713041 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45992427 | CGCCTGTAGTCCCAG[A/C]TACTCGGGAGGCTGA | 51317 |
rs570726255 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45937569 | CACTGCAGCCTCCAC[C/T]TCCTGGGTTCAAGCG | 51317 |
rs570741350 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46049626 | CCCACCTGTCACAGC[A/T]CTCTCCTTGCTGGTT | 51317 |
rs570759319 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46026509 | GGAGAGCATTGAGAC[G/T]TTTTCTCTTGTGGAA | 51317 |
rs570776747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46057675 | AGGTCTCACAAGTGC[A/G]AAAGGTACTAGGCTG | 51317 |
rs570784906 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45939453 | ATTAAGTCAGAAACA[A/C]ATTAAATTCATATGC | 51317 |
rs570813755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46056838 | AGTCAACAATACTCA[C/T]GCTGTCCTCCTCCCC | 51317 |
rs570862219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45983565 | TTAAATATAGATGAC[C/T]GCACTTAGAAACCAG | 51317 |
rs570893162 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930298 | CAGCTGTGTGTAACC[-/A]CCTCCATGCACGCTG | 51317 |
rs570902801 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46041653 | TCCATACATGAAGAC[C/G]CAGATTTAAAACAAA | 51317 |
rs570903790 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46001291 | TGTGACCACCAGGGG[G/T]GCTGGAAATGGGGCT | 51317 |
rs570916186 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46032823 | ATCGCTTCATATTTA[C/T]TGGCCATTAATGATT | 51317 |
rs570920977 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45936270 | GTTGATACAGTGAGA[A/C]CTTGTCTCAAAAAAT | 51317 |
rs570942420 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45992980 | CTGTAGAGTAGAGGT[A/C]AGAAAACTGAAAACT | 51317 |
rs570952032 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45956712 | AAGCATGAAAATGAC[A/G]CACTAAGAAAAAAAT | 51317 |
rs570964415 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46015644 | TTTTAAGTTTTCTAT[A/T]TTTAAATATTTAAAT | 51317 |
rs570964888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46050130 | AATGCTTCACGCCAA[A/G]TTTTAGAAAGAAGAG | 51317 |
rs570996545 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930443 | CCTAACTGCCTCCCT[A/G]TGTCAGGTACAACCA | 51317 |
rs571001433 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46117091 | TGTATTAATTAGTTA[A/C]CTATCTCAACAACTT | 51317 |
rs571018059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46074704 | GACGGGGTTTTGCCA[C/T]GTTGGCCAGGCTAGT | 51317 |
rs571019636 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46117614 | TATACCCCTTTCCAA[A/C]ATCTCAACTACTCTA | 51317 |
rs571049939 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:46117913 | AATGGAATTTTTAAA[-/T]GGACTTACTCAAAAT | 51317 |
rs571056484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45937465 | AGGTTAAAAGTGAAA[C/T]GGGTGTTGTTTTATT | 51317 |
rs571092363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46061884 | ATGTATGGGAGGTAA[A/G]TTTTGTGACCTTGCA | 51317 |
rs571095490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45948176 | AAAAATTTCAGTACC[C/T]TGTTTATGAGCTCAA | 51317 |
rs571148006 | in-del | -/AT | | | intron-variant | PHF21A | GRCh38.p7 | 11:46032876 | CAAGAGTATAAGTAC[-/AT]GTGTGAATGTACATA | 51317 |
rs571154728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45957763 | AAGCAAAAAAAAAAA[A/G]AAAAAAGAAAAAAGA | 51317 |
rs571160797 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46107340 | TCAGTTTCACCATCC[A/G]TAACATTAATTGAGC | 51317 |
rs571171993 | snp | C/G/T | 7.37196e-05 | 0.00607084 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45935731 | ACTTCTGTTTCTCTT[C/G/T]TTCTTTTGCTAAAAA | 51317 |
rs571185298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46097322 | CCACAGGCACTGAGT[A/G]ATTTGGGCCTCTGCC | 51317 |
rs571203660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46045414 | GCTGAGGGGAGTTGG[A/G]AAAGGTAGAGAAAGA | 51317 |
rs571250747 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:46038558 | GTTTATGATATAATA[A/C]CTGAAACTAGGTAAT | 51317 |
rs571255786 | in-del | -/TTCA | | | intron-variant | PHF21A | GRCh38.p7 | 11:45951071 | GGAACGTTAAGACTC[-/TTCA]TTCAAGCCAGAGAGG | 51317 |
rs571269206 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46012715 | CTGCAACCCTACACC[C/T]ACATTTCTAATTCTA | 51317 |
rs571299871 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46046140 | TTTTGCTATTTTCAG[C/G]GTTTGTTTTCAAGAG | 51317 |
rs571322508 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45979279 | CCACCTCAGCCTCCC[A/G]AAGTGCTGGGATTAC | 51317 |
rs571360040 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46034228 | TGCCCCCACCCCCCC[-/T]CTTGCATACTTTTCC | 51317 |
rs571411362 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45952435 | TTTTGCAGAAACAAG[G/T]TCTCACTATGTTTGC | 51317 |
rs571423603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45945027 | CTCGGCCTCCCAAAG[C/T]GTTGGGATTACAGGC | 51317 |
rs571428491 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46021736 | TTTATTTTTTTGTAG[A/C]GATGAGATCCCACTT | 51317 |
rs571431366 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46012678 | GAGGTAAGTAAATCT[A/C]TATCTCTAGTGCTGG | 51317 |
rs571433791 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46006332 | TAAATTCTTAATCTT[G/T]CGGTTGTATATACAA | 51317 |
rs571438656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46028462 | AATCTACTGCATTTT[A/G]AGGAAAAAAAGTTTT | 51317 |
rs571439041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46113204 | TGCATACTGGGACTT[A/G]TAGTAAGTAAACCAC | 51317 |
rs571441086 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:46005404 | ATATATTAACGCCTT[C/G]TATATACCAAATAAT | 51317 |
rs571476802 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46091979 | TGGAACATGCAGGCC[C/T]AGCTGTATTAGCAGA | 51317 |
rs571485029 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45953455 | TCATTCAGAGAGCAG[A/G]TGCCCCTCCTGGTAC | 51317 |
rs571508471 | snp | G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46122639 | TTTTATTAGTGAAAG[G/T]ATTTTATGCCTATTC | 51317 |
rs571531999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45978257 | AGTGAGCCAAGACTG[C/T]GCCACTGCACTCCAG | 51317 |
rs571545752 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45944526 | AGCCACAAAGCCCTG[C/T]GCAACTGGCCCAGCC | 51317 |
rs571554211 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45994358 | TATTTGTCTTTTGAA[A/G]TAGAGCTCAGATAAT | 51317 |
rs571555818 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46004168 | ATTTAAAAATGTTTA[A/T]ATTTATTTTCCATAG | 51317 |
rs571563282 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46018976 | AACACACACATCATG[C/T]AAGAAGCTAAAACTG | 51317 |
rs571568035 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46036147 | TGACTGAATTTCGGA[G/T]ATGAGTGAAAGGGAA | 51317 |
rs571585324 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45980240 | GCAGAGCTCAGATGT[C/T]CTATTATTAACTTAG | 51317 |
rs571595467 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46019992 | TCTACATTTTGACTC[-/T]TTTTTTTTTTTAGCC | 51317 |
rs571649440 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45969299 | GTATGGTCATGCAGA[C/G]CTGCTCGGGCCTAGG | 51317 |
rs571656864 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45977731 | GGTGGTGATTAGGGT[A/G]AAAATTTATGTAGGC | 51317 |
rs571665732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46087871 | AGTGATCCTCCTGCC[C/T]TAGCATCTTGAGTAG | 51317 |
rs571671733 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46095151 | AAAGTGTTTCTTCTG[A/C]AGATTGAATATTAAT | 51317 |
rs571675750 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45977206 | GTGCAGTACGATCTC[G/T]GCTCACTGGAACCTC | 51317 |
rs571682577 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46019474 | AAGATGTGGCCAATC[C/T]AGGCAAAGCTGGCTA | 51317 |
rs571708230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46103542 | ATGTTTTAGGAACAG[A/G]GACAAAATAAAATAT | 51317 |
rs571713861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46044912 | ATTCCATTCAAAAGA[C/T]AGGAACTGATCGAAG | 51317 |
rs571723492 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45961782 | AGCCCCATTTTAGAG[A/C/T]GCTGGAGAGGACAAG | 51317 |
rs571723965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46078982 | TTTCTAAACCCTTAT[A/G]ACCTGAAGATCAATG | 51317 |
rs571730323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46043269 | CCAAGGACTTCTTTC[A/G]AAAGTTATCATGTCC | 51317 |
rs571785788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45961172 | CTTACATCTCCTCTT[C/T]GAACCCACGGTTGCT | 51317 |
rs571795575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46102198 | AAGTGATACACCAGC[C/T]TCGGCCTCCCACAGT | 51317 |
rs571815159 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45977860 | TTTTTTTTTTTTGGT[A/G]TTGAATGGCAGTACA | 51317 |
rs571843164 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46110611 | CCTTATATTTAGCCC[-/T]TTGTATTAACTCCTT | 51317 |
rs571849308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46052058 | GGTTGAGATGATCCA[A/G]GAGTAGCATATGACC | 51317 |
rs571851661 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45948120 | AGGGACACATTACCA[G/T]GTGGAGAAAAGGATC | 51317 |
rs571859930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46112067 | TTTCTGAAGTCAACC[A/G]AAGGCTTGTGGTATG | 51317 |
rs571869854 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45978777 | TATCATTTCCAAATA[C/T]GCCCTTTTTGTGTAT | 51317 |
rs571882152 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45934325 | CTGCCCAGGGAGAAG[A/C]AGCTCTGCTGGCTGC | 51317 |
rs571901588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45987311 | CAAAGACCCTAGACG[C/T]AGTAAATACCTAAGA | 51317 |
rs571908682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45941611 | CCATAGAAATGAATA[C/T]AAAATGCCAAAACAT | 51317 |
rs571930778 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46005398 | TGCACAATATATTAA[C/T]GCCTTGTATATACCA | 51317 |
rs571932717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46006881 | CAGGTACTAACAATA[C/T]GTATTTTCAAAGATC | 51317 |
rs571952668 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PHF21A | GRCh38.p7 | 11:45935001 | GTCACTTCACTCCAA[C/G]AAGGGTGACCTACTC | 51317 |
rs571956380 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46114355 | AAGTGCAATCTGCAT[C/G]AGGAGGCCTAACACA | 51317 |
rs571991955 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46094938 | TTTAAACCTAAGGGA[A/T]CCCCATGAATGGGCT | 51317 |
rs571995777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46059216 | GCTAGGCATACAACA[A/G]TAAAAAACTGGGAAT | 51317 |
rs571998300 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46102914 | TAAGAGAAATAGAAA[C/T]AAAACAGTGGTGGCT | 51317 |
rs572020484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PHF21A | GRCh38.p7 | 11:45934827 | TTTTGCCCTCAGCTT[C/T]CCACACCTGCTGGCT | 51317 |
rs572041474 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45942503 | AATCTTTGGCGCTAG[C/G]AAACAAGATTTCTGA | 51317 |
rs572043181 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | PHF21A, LOC105376661 | GRCh38.p7 | 11:46123257 | TCTATTACCTTGTTA[G/T]GTATTTTCACAAGAG | 51317 |
rs572050173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45985984 | ATTCTCTGCATGGAT[A/G]TTTAACAGATGGCAA | 51317 |
rs572055462 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46043985 | TTGTAGTAAATCAAA[C/T]AAACTGAGGAAAGGT | 51317 |
rs572064145 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46076131 | CAGGCACTGCCTGAA[C/T]TGGTAAAGTGGAGGT | 51317 |
rs572083580 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46087383 | TACTTTCTCCATCAG[A/C]TTGTTGTCTGCTTCT | 51317 |
rs572143646 | in-del | -/TTC | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46044738 | AAAAAAAAATCTGCT[-/TTC]TTAACTATATGCCTG | 51317 |
rs572155929 | in-del | -/AAAT | 0.00517822 | 0.0506191 | intron-variant | PHF21A | GRCh38.p7 | 11:46111475 | GCAAGACTCCGTCTC[-/AAAT]AAATAAATAAATAAA | 51317 |
rs572169383 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45949674 | ACTCTCACCTGCAAG[A/T]CCACGCTGTCCTACA | 51317 |
rs572194721 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46059803 | TCAATCTCGGCTCAC[G/T]GCAACTTCTGCCTCC | 51317 |
rs572199632 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46037387 | TGGCTCATGCCTGTG[A/G]TCCCAGCACTTTGGG | 51317 |
rs572218587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46036257 | ACAGTCATAAGTAAC[A/G]TAACTGGAAACACTG | 51317 |
rs572220269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46076672 | ACACATGAGGAAAAA[C/T]AGCAGTTCTCTTAGA | 51317 |
rs572222857 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46016084 | AGGTTTGTTTACACC[A/G]GCATCACCACAAACA | 51317 |
rs572240947 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46120073 | GCAGAAGAAGAAGAA[G/T]AAGCGGAATTTCCCC | 51317 |
rs572278261 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46082753 | AAAATTGGTATGCTT[C/G]AATTCAGAATATGAA | 51317 |
rs572278349 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46002547 | AAAGGAATTCACACA[C/T]GGCCTTTTTCATTTA | 51317 |
rs572295752 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46013579 | AAGTAGACACAGTCA[C/T]GTGTTGCTTAATAAC | 51317 |
rs572308135 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46051528 | ATGGGTTGAAATTGC[C/G]TAAGGAAACCTCAAA | 51317 |
rs572319221 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:46104489 | CTCTGTTAAAACTGA[C/T]ATATTCCCATGTATT | 51317 |
rs572359727 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46003982 | CTCAGAACAAAAATG[C/T]TTCAATATATTAAGT | 51317 |
rs572365386 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46034287 | TTCATAAGAACTCTT[C/T]ATATGTAAGACTAAT | 51317 |
rs572387875 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45967738 | CCAAGTGTGGCCCAT[G/T]AAAGTCTTGTCGGTA | 51317 |
rs572396691 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46047456 | TAGGAAATATTCCTG[C/G]CTTGTTCTTCTGGAT | 51317 |
rs572406217 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46031399 | TCACTTCCTTGGATA[A/C]ACAACAACAAAGAAT | 51317 |
rs572411480 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:45960165 | GTATGACCCAGCAAT[C/T]TCTACTCCTAGGTAT | 51317 |
rs572427596 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46025821 | TAAGACAGAGTCATC[G/T]GCAGATATGTGATGG | 51317 |
rs572441557 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46085385 | TCTGTTAATATGACA[C/T]CCAGCTTGACCTTCC | 51317 |
rs572454126 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46033082 | ATAATGTTTTATTAG[A/T]TTTTATGTATCCTGT | 51317 |
rs572509715 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:46092220 | CCTTCAGCTCTCTAG[A/C]CCCCTATAACAGAAG | 51317 |
rs572522226 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45959415 | ATTTCCTTGACTTTA[C/T]AAAAAACATTTATGA | 51317 |
rs572536718 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46018105 | AATACAAAAAATTAG[C/T]CGGGCGTAGTGGCGG | 51317 |
rs572546952 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45937642 | CCTGCCACCATGCCC[A/G]GCTAATTTTTATATT | 51317 |
rs572593216 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46022659 | TAGAGACAAGGTCTC[A/C]CTATGTTACCCAGGC | 51317 |
rs572600724 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:45957731 | CACCTTAAGAAACAG[-/A]AAAAGAACTAAATTC | 51317 |
rs572606874 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PHF21A | GRCh38.p7 | 11:45933329 | AGAAGAACCTACTGG[C/T]TGTTCTTGGTGTCAG | 51317 |
rs572612173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46024932 | CTATAAAGCCATCAT[C/T]CCTTATTATTGAACA | 51317 |
rs572621918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46063776 | CAGCTATTAGCAGGA[A/G]CTGATGAGGCTTAGG | 51317 |
rs572626788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46084686 | AGAATCATAATTTTT[C/T]TTTTTTTTTTTGAGA | 51317 |
rs572632522 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45973670 | GTAGTGTAACAGCAA[A/G]GACTGACTGCATTAT | 51317 |
rs572641095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46101726 | TCGCAGCCTCGACCT[A/G]CCAGGCTTAATCAAT | 51317 |
rs572641708 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45992756 | AAGACACAGGGAAAC[A/C]CACAACTATATACAA | 51317 |
rs572680611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46101111 | CACAGACAGGAAAGT[A/G]TACATAAAATAAAAT | 51317 |
rs572716786 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45969706 | GAATGTTTAGCTAAG[C/T]GGGATAGACAGCTGG | 51317 |
rs572720018 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:45939174 | GGAGAGGTCTATAGT[C/T]GCCAAGGCCAAAATT | 51317 |
rs572733008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45963934 | CTGGGCGTGGTGGCT[C/T]ATGCCTGTAATCCCA | 51317 |
rs572762941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46030385 | TTACCAAATGATTTG[C/T]CCAGGTTTTCATCAT | 51317 |
rs572775576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46022359 | ACTCAGGATGCTGAG[A/G]TAGGAGGATCACTTT | 51317 |
rs572799734 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46056471 | TTAGTATGAGCTAAT[A/G]TCACAGTGAAGATTT | 51317 |
rs572841291 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:45963008 | AAAAGCTCTATCAAC[G/T]TGAAGGCCACGACAG | 51317 |
rs572850666 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:46038777 | ATAAAACCACTAGTT[C/T]CACTCCCATGATAAC | 51317 |
rs572850771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46029795 | ATAACAAATGTCCGT[C/T]AGAGTGCTTTTAGTT | 51317 |
rs572853591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45955828 | CCAGGTGTGAGGAAC[A/G]GAACCTCCAGCCAAC | 51317 |
rs572873174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46006590 | CTGCCTGAGCTAGAG[A/G]ATGAAGTTATGCCTT | 51317 |
rs572884197 | in-del | -/C | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:45984780 | TGGATGTCAGTGCTG[-/C]CAAGTCTCTGCTTTT | 51317 |
rs572890126 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46015023 | ATAAAAAAAAATAAA[A/T]AAATAAAAAATAGTT | 51317 |
rs572910282 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46005750 | AATATTTGTAGCACA[A/G]TTAAGCTTCCATAGC | 51317 |
rs572920106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45972679 | AGCACTTTGGGAGGC[C/T]GATGCGGGTGGATTG | 51317 |
rs572934818 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46061898 | AGTTTTGTGACCTTG[C/T]ATGTCTTAAAATGTC | 51317 |
rs572952231 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46043364 | GACACAGGTTACTTC[G/T]GTTTACCCACATCAT | 51317 |
rs572953522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46089027 | CATTTCTTTAACTAA[C/T]GATAAGTCCATGACA | 51317 |
rs572962957 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930111 | AATAAGAAGGACCAC[A/G]CCCTATAAGAGAATG | 51317 |
rs572997942 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45988826 | AACTCAGGAGGTGGA[A/G]GTTGCAGTGAGCCAT | 51317 |
rs573014682 | snp | A/C/G | 0.00795819 | 0.0626103 | intron-variant | PHF21A | GRCh38.p7 | 11:46069292 | GGCAATAAACTCAAC[A/C/G]AACAATTGGACCAAT | 51317 |
rs573015222 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45946449 | AGTGCTGTGGCACGA[C/T]CTCGGCTCACTGCAA | 51317 |
rs573043429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45979611 | TACAAGTGATACTTA[C/T]CTGGGTTATACTGTA | 51317 |
rs573054818 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46021573 | GTTCAGAGACAGGGT[A/C]TCACCCTGTCATCCA | 51317 |
rs573067264 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45960185 | CTCCTAGGTATATAC[C/T]CTAAAGAACTGAAAA | 51317 |
rs573069498 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45957423 | TAGAAAGACTAGAAT[A/C]ACATAAAATCTCTTC | 51317 |
rs573071095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46080186 | TTTTTTGAGACAGGG[C/T]CTTGCTCTGTCACCT | 51317 |
rs573152258 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45994580 | CCACAGGCCTAATGT[A/G]TGTGATGCTGAATTT | 51317 |
rs573180294 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | PHF21A | GRCh38.p7 | 11:46011690 | CCGCAGAATACAGAT[A/G]TTCTTTCAAGCAATG | 51317 |
rs573182865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46053541 | CTTCATTATATATAT[A/G]ATTATATGTATACCA | 51317 |
rs573201457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46113488 | AAATAGTTTTTTAAA[A/G]TTTGAATGGATCCAT | 51317 |
rs573227692 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46045503 | GTCTAATTACTTGCT[A/T]TATTTTACCCAAGTA | 51317 |
rs573231763 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45949096 | GCTCAAGGGTTTTAT[G/T]GTATGTACTTGGCTC | 51317 |
rs573239570 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45998343 | GGATGTTAGGGCCAT[C/G]GATAGAGTGGTAGGC | 51317 |
rs573248766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46104686 | CAATAATAATGATAA[A/G]AGCAGCTATCATGAT | 51317 |
rs573253584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46080088 | TTTGTCACTCTCTTT[C/T]GGTGACAAGGCACTT | 51317 |
rs573260323 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46054364 | GTCCCCAGATGATTC[A/G]GGAATAAAAATGCTA | 51317 |
rs573260889 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45929564 | GACCTCTGGCCTGCC[C/T]GTCCCATCCCGCCTG | 51317 |
rs573269970 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45981346 | AGCCAAGATCATGCC[A/G]TTGCACTCTGCACTC | 51317 |
rs573273368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45944672 | GCTGTTCCCTCTGCC[C/T]GGCAGGCTCTTCCCC | 51317 |
rs573295638 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46045120 | GCCTTAGCTTGTGTG[A/C]TTCCCCTGACTTAGA | 51317 |
rs573312641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46079227 | TCCCTATGGCTAATC[A/G]GGTTTGGACCAAAAA | 51317 |
rs573349423 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45936762 | TAGGAGAATCAAGTT[C/T]AAGGCAGGAAGAGCC | 51317 |
rs573362286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45953923 | TATAGAAATACGGTA[C/T]AGGTTGTCCTTTCTG | 51317 |
rs573369108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45961277 | ATCAAGTATACTTTA[C/T]ATACTTGTCTGCATG | 51317 |
rs573369554 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46090868 | ACACTAAGCTTGTGG[C/G]AGTTATTTATATCCT | 51317 |
rs573379621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46028730 | AGGCGCCCGCCACCA[C/T]GCCCAGCTAATTTCT | 51317 |
rs573394699 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46054477 | TTTTTATGCCTGGGC[A/G]CCATTCTCGAAGATT | 51317 |
rs573408003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46019712 | GTCGTATTAGTCTCC[A/G]GTTAGATTTAACTGG | 51317 |
rs573411441 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45945325 | AGGGCTACTAAGTAT[C/T]TGACAGTTTTTCCGG | 51317 |
rs573414671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45952810 | AATTACTGGCCAAAT[A/G]AAATCTGTCAGATAT | 51317 |
rs573493703 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46020551 | TTTCTGCTTCCCTTG[C/T]GTCTAACACCATCTG | 51317 |
rs573501381 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45951918 | TTCAAGCTATTCTCC[A/G]GCCTCAGCCTCCCGA | 51317 |
rs573509675 | in-del | -/A | 0.40853 | 0.193309 | intron-variant | PHF21A | GRCh38.p7 | 11:46096288 | TAAAAAATAATAATT[-/A]AAAAAAAAAAACCCT | 51317 |
rs573513402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46019333 | ATGTCAAATGAATCA[C/T]CTTAATTTTTTTCAC | 51317 |
rs573567980 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46029740 | CTAAAAACCTAGCAA[A/T]AAATTTCATGTCATT | 51317 |
rs573592653 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46096502 | AATCCAACAGAAAAT[-/A]AGTCTTCACTTCCTT | 51317 |
rs573628970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45970907 | AGATAATGCACTGAA[C/T]TTAGTCCTTGGTGTC | 51317 |
rs573633684 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45981877 | AATCTTTAAGTAAAA[A/T]AAAAAGTTCTCTTGA | 51317 |
rs573638102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46045475 | ATGTTTTTAGGACAC[C/T]ACTATTACTCCAGTC | 51317 |
rs573663195 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46012870 | TACTTCATCACATCC[C/G]CCCAACTCTTTACAT | 51317 |
rs573668022 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46022298 | ATTTCTACAAAAAAA[G/T]TTAAAAATTAGCCAG | 51317 |
rs573674039 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46016921 | AACATGATGTGCCCT[A/G]ATGTGATGAAGTCAC | 51317 |
rs573677029 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45962825 | ATGAACCCGGGAGGC[A/G]GAGCTTGCAGTGAGC | 51317 |
rs573727895 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45979462 | TACCTCCAAAAATTC[A/C]AAATAAGGTTTTAAT | 51317 |
rs573735850 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45977695 | GTCAGTTTTGAATGC[C/T]TAATTTCCAAATAGC | 51317 |
rs573746492 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45935834 | GCCAAAGAAGGTATT[A/T]TCCCCAGAGCTCCCA | 51317 |
rs573748427 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46096685 | TTAAAATGTGGAACT[A/G]TCCCAGGACTCAGTT | 51317 |
rs573795023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45996725 | TAGGATCCCAATTAT[C/T]TGGGAAACAAAAGGT | 51317 |
rs573798252 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45974217 | ATTTACTATTTATTG[A/C]CACCAAGACCCAGGT | 51317 |
rs573805648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46038310 | TTTTTGTATTTTTAG[C/T]AGATACGGGGTTTCA | 51317 |
rs573806588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46021470 | TTCATCCTGGGCCCA[A/G]GCATCACCAAGGGTG | 51317 |
rs573808100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46052737 | CCTCTGAAATCTTTA[C/T]CAAAGCAGTTAATCA | 51317 |
rs573828657 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45975141 | CAACATAGTGAAACT[C/T]CACCTCTACAAAAAA | 51317 |
rs573831750 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:45956281 | TATAAAAGCCAGTGT[A/T]ATTATTTATTTTTAA | 51317 |
rs573839251 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45957292 | CAATTAGACCTGTCA[A/G]GCATAGAAAGAATAC | 51317 |
rs573849177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46105350 | AGTGCTTTCCAAGCA[C/T]GTGTGCCAGACGTCT | 51317 |
rs573865421 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46086359 | CTCCTGACCTCGTGA[G/T]CCGCCCGTCCTGGCC | 51317 |
rs573874955 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45987123 | CAGTGGCTCATGCCT[C/G]TAGTCCCAGCTACTT | 51317 |
rs573884045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46104582 | ACTCTTTCTCACCAC[A/G]CATTTCAAGGGAGAA | 51317 |
rs573942015 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46004671 | GCATAGCACAGACTA[C/T]TACTTTTTCATAGCA | 51317 |
rs573949750 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45932063 | GCAAGACAGAGCGAA[C/G]GCCACGCTGGGGCTC | 51317 |
rs573976320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46061100 | TTTTCGTCAGGTTTG[C/T]CAAAGATCAGGTAGC | 51317 |
rs573994088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45978612 | GTAAGAGGTATCCAC[A/G]CTTAGGTTTCAGAGG | 51317 |
rs573998145 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45988698 | GTTCGAGACCAGCCT[C/G]GCCAACATGGCAAAA | 51317 |
rs574004761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45944539 | TGCGCAACTGGCCCA[A/G]CCACTTCTGAGGCCT | 51317 |
rs574013371 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46122154 | CCCCCTCCCGCCGGC[A/G]GGAGCTGCAAAGGGG | 51317 |
rs574014007 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45948761 | ATTCTCAGAGAACAA[A/C]AACAAAACTATTTTC | 51317 |
rs574015270 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46069824 | TTCTAAGCTTCTTAG[A/C]AAAGTAGTACTTTAC | 51317 |
rs574026997 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46005502 | TATTAACTTAATTAA[C/T]GGGCACCAAATGTTC | 51317 |
rs574041113 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46115558 | AGCAAAAACATACAC[A/C]TGAGAAAATTAATGT | 51317 |
rs574056330 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:45995748 | ACGCAGCTCTGTTAC[C/T]TATTGGCACACATAT | 51317 |
rs574062198 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46062020 | TCCAATGACTGCTAG[C/T]TTTCTTTGTTGCTGC | 51317 |
rs574063409 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46009675 | AACATTCCAAAAGTA[C/G]CAAATAGCAGAGCCA | 51317 |
rs574095278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45943764 | GGTGGAAAAATCTGA[C/T]AGAAACTATCTTAGG | 51317 |
rs574098303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46009000 | TTTTTTTTTGGAGAC[A/G]GAGTCTCACTGTCGC | 51317 |
rs574115910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45977841 | TTTTTTTTCTTCTTC[C/T]TCTTTTTTTTTTTTT | 51317 |
rs574158965 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46118590 | TAACTGTACACAAAA[C/T]TTCCTCTTTGCCATG | 51317 |
rs574174131 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46103876 | CTGGTTTCACTTATA[A/G]GATAGAGACATTCGT | 51317 |
rs574174619 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46099346 | GATAGCCAAGAATAA[C/T]CAGAGTACTTCCAGA | 51317 |
rs574189166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46094091 | AATATATAAAATATG[C/T]TGAAATTCAAAGTGA | 51317 |
rs574197117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45952557 | ATTTCACAAGTTCCT[C/T]AGCAATTTTTGTGAC | 51317 |
rs574197924 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46095048 | GGTCCACGGCTTTAA[A/T]TGGTTTCACAATGAG | 51317 |
rs574213884 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46112666 | TATTCAAGATGTTGA[C/G]AATTATTACAGAAGA | 51317 |
rs574238167 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46076989 | ATCACCTAATGCACA[G/T]ATCCTAAATACAGGC | 51317 |
rs574244461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46087044 | ATAATAATACTCTGA[A/G]CTGTCTAGAATTTGT | 51317 |
rs574272942 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45992231 | GAAAGTGGAATTAGA[C/T]ATTACTTAGAAAATT | 51317 |
rs574282979 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:46027634 | AAGATCTTTAAAATA[C/G]CCAAGTGCTAAAGAC | 51317 |
rs574325450 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46086427 | CCCAGCCAGCTATTA[A/T]CTTTTAAAATATTTG | 51317 |
rs574382153 | in-del | -/AGGAAAGGAAAGGAAAG | 0.00874735 | 0.0655527 | intron-variant | PHF21A | GRCh38.p7 | 11:46079835 | CCCAAACAAATGGAA[-/AGGAAAGGAAAGGAAAG]AGGAAAGGAAAGGAA | 51317 |
rs574382447 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46016053 | TGCTATAGTTTTATA[C/T]GACTGGCAGCACAGT | 51317 |
rs574385605 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45961180 | TCCTCTTCGAACCCA[C/T]GGTTGCTGGAATTTG | 51317 |
rs574409693 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45960459 | ATCACATATTGTATG[A/T]TTCTATGTATATGAA | 51317 |
rs574420615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46015371 | AATGTCAATTTTTGT[C/T]TTTGTTACAATTACT | 51317 |
rs574421119 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45932268 | TGGCTGAAAGACCAA[A/G]AGCAGCACCAAAGGA | 51317 |
rs574438017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46049790 | ACCCATTAGAGTCAC[A/G]AATAGCAAACTGCTG | 51317 |
rs574443328 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46063103 | CTATAAGAGAGAAGT[C/G]GGGAGAGGAATAGAG | 51317 |
rs574452495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46001532 | CAACAGACCACCTAA[C/T]AACATAGGGAGGAAA | 51317 |
rs574459424 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46049099 | CCAAGTTTTAGAAAG[C/G]AGAGATTATCATTGT | 51317 |
rs574459996 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46099460 | CCTCACTTCTCAATA[C/T]AGCACTGCTGTACTC | 51317 |
rs574464078 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45981172 | GGGTGGATCACTTGA[C/G]GTCAGGAGTTCAAGA | 51317 |
rs574475057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46067075 | TGTATTCTTTACTAA[C/T]GCACCTTATGTATTA | 51317 |
rs574475425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46058105 | ATCTCACTTAAACCT[A/G]CAGAAAACAGAAACT | 51317 |
rs574525296 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45965729 | TAATGTTCATTTTGG[G/T]ACATTAATTCTATAG | 51317 |
rs574526488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46083516 | ATTGTTACAAATTCA[A/G]AAGTAGTCAATGCAT | 51317 |
rs574533145 | snp | A/C | 6.62815e-05 | 0.00575642 | intron-variant | PHF21A | GRCh38.p7 | 11:45965286 | ACGACAAGGCTACTG[A/C]CCAGAGCAGGTACAT | 51317 |
rs574533658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45990088 | AAATTACAAAATCTA[A/G]TTACAAAATCTAATC | 51317 |
rs574542741 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46067897 | AGTACCATGAGTACA[C/G]AGAAGAGGAGTGTCT | 51317 |
rs574556613 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45940407 | CACCATGTTGGTCAG[C/G]CTGGTCTCGAACTCC | 51317 |
rs574561767 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46023229 | GCAGTTTAAGTGTAA[C/G]CAATGGTTTCTTAGC | 51317 |
rs574577949 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PHF21A | GRCh38.p7 | 11:46008148 | TTAACATTTCAGCAC[C/T]TTCCCCTACAATGTG | 51317 |
rs574594248 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45973430 | TTTTCTGCCTTATGC[A/G]CATATACACATATTA | 51317 |
rs574608208 | in-del | -/CA | 0.00159617 | 0.0282053 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45932414 | GCACCAAGAAGAGAG[-/CA]CACGGTCTTTTCTGA | 51317 |
rs574616703 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:45955047 | TACTGTGGCAACCAG[-/T]TGCTCTGGGGCACAA | 51317 |
rs574636460 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46073372 | ATTAGAGTGGTTCAT[A/G]TATTTAATACCATGA | 51317 |
rs574690751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45954784 | TGTGGAAGTAATGCT[C/T]CTTTCATATGGCAAC | 51317 |
rs574702846 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | PHF21A | GRCh38.p7 | 11:46023894 | CCAGGAGGCGGAGGT[G/T]GCAGTGAGCCAAGAT | 51317 |
rs574719468 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46072654 | AAAGTATGGTTCAAT[A/G]TGAGATAATAATAGA | 51317 |
rs574728734 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45990855 | CACATAGCAGAACAT[C/T]TGTTACAATCGAACC | 51317 |
rs574748626 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930834 | AAGAGCAGCGGAGGG[A/G]AGGAGGAGGAAGCAA | 51317 |
rs574767839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45938607 | ATATGTTTTTCTATA[C/T]ACACAGACCCACAAT | 51317 |
rs574769859 | in-del | -/TGGC | 0.0126979 | 0.078662 | intron-variant | PHF21A | GRCh38.p7 | 11:45989728 | TTTAGCTGGGCACAG[-/TGGC]TGGCTCATGCCTATA | 51317 |
rs574773457 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46002865 | AGAACAAAGCAAAAC[-/A]AAAAAAACACCCAAT | 51317 |
rs574777867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46098610 | GTCTAATGATCATAA[C/T]GAAAACTTCTTAATT | 51317 |
rs574781117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46106682 | TAACATGCATGCTGC[A/G]TACTCCACAATGTTA | 51317 |
rs574819171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46090744 | AATGTGGTATTCAAT[A/G]TGTACCTGAATAACA | 51317 |
rs574827404 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45946365 | GCCCAGTGGGAGCCA[G/T]GGCCAGGAATGAGTT | 51317 |
rs574855899 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45960372 | CAGCCATTTAAAATA[C/G]AAGGGGGCACTGATA | 51317 |
rs574857070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46059179 | CGTACAAATATTTAC[A/G]TCCAAGGATGTACAC | 51317 |
rs574857100 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46097195 | GGTATATTCTCTCGC[A/G]AGCCAGAGTAAGCTT | 51317 |
rs574861110 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46047787 | TCTGCATGGTGAGGT[C/G]CAGTGGGGATCAAAT | 51317 |
rs574873209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46039028 | AGAGAACAGCAAGGA[A/G]CCCAAAATTACTGGA | 51317 |
rs574896703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46015090 | GATTTGCATTTCTTT[A/G]ATGATTAGCAATGTT | 51317 |
rs574902774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46007293 | CTTTACAGAAGATAC[C/T]TCCATCTACCTTTTT | 51317 |
rs574907550 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45931187 | CCTAGCCCCGTCCTC[C/T]GACCCAAGACTCCTA | 51317 |
rs574921467 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45991114 | CTTTCCAGAATGTCA[C/T]AGAGTTGGAGTCATA | 51317 |
rs574923110 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46063740 | AATACTAGAAATTTA[A/G]AGAGTTATATATAAT | 51317 |
rs574958971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46048221 | CTCCAGGGAGGTGCA[C/T]ATTCTAAACATTTTT | 51317 |
rs574993810 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45992055 | CTAGGCATGATAGGG[A/C]CTGACATCAACTGGA | 51317 |
rs575002343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45937983 | AATATGGCAGAGGGC[C/T]TCTGAGGGAATGAAG | 51317 |
rs575003144 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46062864 | ACAAAGACTTGGACA[A/T]GAATGTTCAAATTAA | 51317 |
rs575012278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45998953 | TCAGCCTCCCTCCCG[A/G]ATAGCTGGGATTACA | 51317 |
rs575026048 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46040238 | AACAGAGTTTCATTA[A/C]ACATAATGGTCTCAC | 51317 |
rs575032799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46055291 | TGGATTTCATGAAAA[C/T]AACTTGGTTTTTTAA | 51317 |
rs575051775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46056035 | TCTTTATAGCTCAAG[C/T]AATACTTTCTCAATG | 51317 |
rs575059187 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46115317 | TGAATTGAGGGACAA[A/G]TAATAGAAAAGTTAT | 51317 |
rs575076444 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46076016 | CACTCTTTCTAACCA[C/G]AGGGAGAGTGGTGGG | 51317 |
rs575077171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46102477 | ACAAATCAAGGAAAG[A/G]AAGCCTAGTCTTCTC | 51317 |
rs575095273 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46008056 | CTACCCACCAACTGG[G/T]AGGTGAAAATTAACA | 51317 |
rs575160333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46046813 | GAGTGTCTGGACAAA[C/T]GAGAGTAGTTTCCAA | 51317 |
rs575178611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46023047 | TGAGCCACCGCGCCC[A/G]GCCTTGTTATTTTCT | 51317 |
rs575207075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45998818 | AGCCACCACACCCGG[C/T]CTTTTTTTGTTTTTG | 51317 |
rs575209091 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:45988997 | ATATTTGTTACAATC[A/G]CTTAAAGAAAAAAAT | 51317 |
rs575244033 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46062614 | GCCTGTTCTGACTTG[A/C]ACATTAGCAGCTTCC | 51317 |
rs575251342 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45948442 | TACCTCTTTCCTTCC[C/T]GGAAAGTCTGCAGCT | 51317 |
rs575306514 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46065911 | AGAGCAAGGAGCTAC[G/T]GGCTCACAGAAGAGA | 51317 |
rs575352962 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46015750 | CACAATCATCAATAT[C/T]ACTGTCTTTTACCTC | 51317 |
rs575368798 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46040618 | ACCAAAAATAACAGT[A/G]TGTGCTGAAGGACTG | 51317 |
rs575386158 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45999546 | CAAATGTACTTCAAA[A/C]TGCAAGCTTATTTTG | 51317 |
rs575402558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46107805 | CTTTAGTATGTCTTT[C/T]TAAATATAATGCCAG | 51317 |
rs575429389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45956817 | GCGTAAGTCCCTCCT[C/T]ACCAGTAATCACTTA | 51317 |
rs575441721 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | PHF21A | GRCh38.p7 | 11:46116578 | CTTTTTTTTTTTTTT[A/T]AATTATGAGAAACTG | 51317 |
rs575476209 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45961990 | GTTGGTTATGTCTGA[C/G]AGGGGAAGGACACGT | 51317 |
rs575485017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46014464 | TGTGAATAGTGTGGC[A/G]ATGAACATACAAGTG | 51317 |
rs575574779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46045763 | GAAGCCCTACTCTTG[C/T]CTTCTGTGAGTTTCT | 51317 |
rs575584496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45994498 | CTCCTCCACGTATCA[A/G]GCAAGACCAGGGCTC | 51317 |
rs575601486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46105713 | GAGAAAAAAGCAAAA[C/T]TCTCATAATTTTGTA | 51317 |
rs575631197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46098570 | ATTCACAAGCTTCCA[C/T]AGCTCTCACGAAGCT | 51317 |
rs575633405 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45984770 | CCCTCCACAACTGGA[A/T]GTCAGTGCTGCAAGT | 51317 |
rs575634713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46082243 | TTTCTATCCAGTAAG[C/T]TCAATTTCAGCCCTA | 51317 |
rs575637982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46111561 | AACAATATTGTAAGA[A/G]CTCCTCGCAAGAGAA | 51317 |
rs575670640 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45993816 | AGTGATGCTGGGAAA[C/T]GGGACGGTCAGAGAT | 51317 |
rs575688055 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46091436 | AACCTCTCAAAGTAG[A/G]TATTAGGAAAAAATG | 51317 |
rs575691946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46055230 | AAATATAACAAAGCA[A/G]CAAATTTTTAGTAAT | 51317 |
rs575698070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45936951 | CTTGACCTGACATGG[A/G]CTGCCTGTCTCAATT | 51317 |
rs575721146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46023046 | ATGAGCCACCGCGCC[C/T]GGCCTTGTTATTTTC | 51317 |
rs575728217 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45953708 | TTTAATAGTAGTAGT[A/C]AAGAAGAAAGAAGAC | 51317 |
rs575743577 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46071793 | TTTAAAAAATCATGA[A/T]ATAGCCAATTATGCT | 51317 |
rs575745235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45985916 | GTACAAATAAACAAA[C/T]TGACAACAGCAGCAA | 51317 |
rs575753684 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46059011 | TGCCCCAGGGTCACC[C/T]AAGATGCCCTAATAC | 51317 |
rs575775285 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45953066 | CATTTGGGGTTTGGG[A/G]TTCTAATGTAATACA | 51317 |
rs575799679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45945339 | TTTGACAGTTTTTCC[A/G]GAACCTGTTTCTGAT | 51317 |
rs575803435 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:45938693 | ACAGAACAATTATAA[C/T]GATATACTGTAATAA | 51317 |
rs575812911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45949253 | AGTGACTAATAAAAA[C/T]GATAAGTCAAAAAAA | 51317 |
rs575816880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46013112 | AACTTATTTAAACCC[A/G]GTTAAACTGGGTATT | 51317 |
rs575836205 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930209 | CCCAAGAGAGAAGTA[C/T]CAGAGGTGGCTGGAG | 51317 |
rs575850492 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46046610 | AATCATTTTGTGCAT[A/G]TATTTCCCTCATATA | 51317 |
rs575865434 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45953836 | TAAATTGCATGGCTA[C/G]AGTAAATATGAATCT | 51317 |
rs575883754 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46013642 | CATTTCATTGCTGTG[A/C]GAACATCATACAATG | 51317 |
rs575889317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46120018 | GGGAGGGCCGGCCCC[A/G]GGGTGAGGGGTGCAG | 51317 |
rs575906381 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45944729 | TTCATAAACATCAGC[A/C]TCCTGCCAGTATGCT | 51317 |
rs575924838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46110942 | AGGCACCTGCCACCA[C/T]GCCCAGCTAATTTTC | 51317 |
rs575928379 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46005946 | TAAGAAAAATAAAAC[A/T]TACAATTTTAAAAGT | 51317 |
rs575930724 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46021414 | AACTATTAACAAGTA[C/T]ACACCATACCTCCAT | 51317 |
rs575943036 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45945343 | ACAGTTTTTCCGGAA[C/G]CTGTTTCTGATCAAC | 51317 |
rs575954129 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46101899 | GAGTCTCGCTCTGTC[A/G]CCAGGCTGGAAGCAG | 51317 |
rs575979251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46054474 | ATCTTTTTATGCCTG[A/G]GCGCCATTCTCGAAG | 51317 |
rs575993818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45966393 | ATGATTCCTACCCCA[C/T]CCTCTACTCTCTAAA | 51317 |
rs575994879 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46003146 | TAGAATAATTTCCTC[A/C]ATAGAATCTTTTTAA | 51317 |
rs576048171 | snp | C/G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46094028 | GGTAAACCACAGAAT[C/G/T]GGAGGTGATAATTAT | 51317 |
rs576067970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46094488 | ACTTTCTCTTAACCC[A/G]CTGCAGGAGTTACTC | 51317 |
rs576075151 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46083914 | GATTTCTTTCTTTTT[A/T]GTTAACACCTTTGGT | 51317 |
rs576076718 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46073214 | GCGCCTGTAGTCCCA[A/G]CTACTTGGGAGGCTG | 51317 |
rs576084825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46042779 | TTTCCCCTTCTGCCA[C/T]AGATAGCACCTTCTT | 51317 |
rs576086040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45934384 | CTCAGTGGAGTGGGC[A/G]GCTACCACCTAAGGA | 51317 |
rs576087165 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46111114 | AAATCACAACTATGT[-/G]GGGGGGGGAGGCTAG | 51317 |
rs576095963 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46034674 | TATGGCTGTGCTACT[C/T]GCCTCCTTTCCTGGG | 51317 |
rs576106940 | snp | C/G | 0.00157169 | 0.0279888 | intron-variant | PHF21A | GRCh38.p7 | 11:45935565 | GGGCCCACACGTACT[C/G]TTACGTATATTGGAA | 51317 |
rs576151315 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46010538 | GTTTGGGAATAGTGG[C/T]ATGAATAACTCAAAA | 51317 |
rs576157079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46058339 | TGTCACATTGTTGGT[A/G]AAACGAAACCTGATT | 51317 |
rs576157310 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46009757 | ACTGCACAATACAAT[A/T]AATATAATTCTGCTC | 51317 |
rs576191922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46067281 | AAGAAACGACACAGC[A/G]TAACAAGTATCTGAA | 51317 |
rs576194857 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46024851 | TCTTTAAGAATAAAC[C/G]TGCCATCCTGATGAT | 51317 |
rs576202965 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45967457 | CCCTAAGTGGGGTGA[C/G]TCTCATAACTTGGGC | 51317 |
rs576289559 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46113438 | AAATGCTGAAAAAGC[-/A]AAAAAAACTTGATGA | 51317 |
rs576294319 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PHF21A | GRCh38.p7 | 11:45933230 | ATAACCACGGAGATG[A/C]GCGACTCACCAAGCA | 51317 |
rs576349043 | snp | C/T | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45975214 | AACTACTTGAGAGGC[C/T]GAGGTGGAAGGATCA | 51317 |
rs576355672 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45932190 | CGGCCAGGGTGCGTG[A/C]GCACCACAGAGCTCC | 51317 |
rs576357122 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46033103 | TGTATCCTGTGACTT[C/G]TATTTTTTCCCAAGT | 51317 |
rs576377533 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46050463 | AGGGAGGCAAATTCC[A/C]TAGCTGCCGAATCAC | 51317 |
rs576389839 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46069354 | AACTAGACTAAATCT[C/T]AGGAAATTCCTAGGC | 51317 |
rs576401913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46032924 | TATACATACATGTAC[A/G]TATAATCTCTAATAA | 51317 |
rs576471086 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46119212 | CTAACTTTCCCAGCT[C/G]GAGCATCTACATTCC | 51317 |
rs576475672 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45997616 | TTTCTTTCACTAAAT[A/G]CTTGTTTTGCAGCCT | 51317 |
rs576519146 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PHF21A | GRCh38.p7 | 11:45933037 | ACACACCTGGGTCGC[A/G]TGCTGCTTCACTCAA | 51317 |
rs576530724 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45983700 | AGCTGGCTTTTCTAA[C/G]TCTCACAATCCAGTC | 51317 |
rs576531456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46100294 | AAAATCCCATGAGCA[C/T]GGACTTTTTTCCTAA | 51317 |
rs576567075 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45939669 | ACCACCCCCATCACA[C/G]TGATAGTGTTAGGAC | 51317 |
rs576589021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46000329 | AGAAGCTAAGCACTA[C/T]TTCTTCATACTCTAC | 51317 |
rs576602271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46025621 | AAAAAATTTTCACTT[C/T]GACACAATTTCAGGG | 51317 |
rs576608550 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45966791 | CGCCCAGCTAATTTT[C/G]TATTTTTAGTACGGA | 51317 |
rs576615241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46032143 | AGAGCAATGTCCTGT[A/G]TCCTTAGTTAGGATC | 51317 |
rs576629434 | snp | A/G | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46041763 | ATAAATCAGATACCT[A/G]TATACCCTTCCACGC | 51317 |
rs576656403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46100928 | TCCCTCCTTGACAAA[C/T]CATTTTATAAGTGAA | 51317 |
rs576679413 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46118215 | CCAGGTAGGTGTCTT[C/T]TTCATCTATTACTAC | 51317 |
rs576684526 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45991627 | AAAAATAAGTAGAGA[C/G]GCAGTATTGTGCTGT | 51317 |
rs576717092 | snp | C/G | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46108703 | TAACTTAGATGCACA[C/G]CTTTTGTAATATTTC | 51317 |
rs576726423 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46062544 | AATATCTTCTTTTAC[A/G]GATCTAGGGATCTAA | 51317 |
rs576744356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46110896 | GTTCAAGCGATTCTC[C/T]TGCCTCAGCCTCCCG | 51317 |
rs576747946 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:45990995 | TATACTATCACACAG[A/G]GTAGTTTCACTGTCC | 51317 |
rs576756906 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46049935 | CTTATTTTAATTTTG[C/T]ATATTTGTCAGACCT | 51317 |
rs576763527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46009120 | GCTGGGATTACAGGC[A/G]TGCATCACCATGCCC | 51317 |
rs576773328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46110018 | GGTCTATTGGGAGCA[A/G]GGTGGATCACTAATT | 51317 |
rs576785699 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46091572 | AGCTAACTAATCCAA[A/T]ATTAATTTTAAGAAT | 51317 |
rs576837086 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45932022 | AGGCAGAGAAAGGAG[C/T]GGGAGCTTCAGACCT | 51317 |
rs576849888 | snp | A/C | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45932672 | CTTAATTTAAGTAAC[A/C]CTAGGAAGACCTCAA | 51317 |
rs576874052 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46090961 | AATGGGTTAAGGTCG[C/T]TTCTCTAAGATTCCA | 51317 |
rs576879863 | snp | A/T | | | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45929436 | AACAAACAAAAACAA[A/T]AACTTTGAAGCACAA | 51317 |
rs576930820 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | PHF21A | GRCh38.p7 | 11:46074463 | GCTCTTTTGGCGGGA[C/G]GGGGGAAGGCATATA | 51317 |
rs576931479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45974307 | AAACCAAACTCCTGG[A/G]TTTAGATGACAAAAG | 51317 |
rs576933497 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46114539 | AAAGTGACGGGCTAC[C/T]ATAAAGGATTTGAAG | 51317 |
rs576940575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45957199 | ATAAATGGAGACTTC[A/G]ATATCCCTCTTTAAG | 51317 |
rs576944885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46058298 | GAAACATTATAGATG[C/T]TTCCTTTTTACACTA | 51317 |
rs576964713 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46074931 | ATGATATTTTTCTGT[C/T]CCATCAAGAAGGTTG | 51317 |
rs576969239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46072779 | CCAGGTAAAGGGAGA[C/T]AGGGCAGCAAACTGT | 51317 |
rs576988117 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46016299 | TCATTTCATGACTCA[A/C]AATTTCCCAGAGTCT | 51317 |
rs576991080 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46096255 | TCATCATTACTGGAT[A/C]ATTTTGTTCCTTCTA | 51317 |
rs576997474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46074445 | TCTGCCAGAGGATAA[A/G]TGGCTCTTTTGGCGG | 51317 |
rs577026373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45949151 | GCCTCTGTTGCCGAT[A/G]ACAGCTGTATTGAAG | 51317 |
rs577083953 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45958203 | AAGAATTAGCACCAA[G/T]CTGTCTCAAATTCCA | 51317 |
rs577106842 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46099747 | AACATTTATTTCAGT[G/T]AAAAGGTTTTGGCAA | 51317 |
rs577107776 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46066387 | CAACAGTTTTTAAAA[A/G]TTAATATGTGTTCCT | 51317 |
rs577108807 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46107945 | TGGGGATGAGGTCAG[C/T]CCACACTACTCACAT | 51317 |
rs577132362 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46066335 | ATATGTACATACATA[C/T]AAATATATATTAGAT | 51317 |
rs577152670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46040938 | ACACACACACACGCA[C/T]GCACAATTAAGGTTC | 51317 |
rs577170633 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46101883 | TTTTTTTTTAAATAC[A/G]GAGTCTCGCTCTGTC | 51317 |
rs577179684 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46088134 | TTATAGCATCAAAAG[A/T]ATTATTGGCTACATT | 51317 |
rs577183408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45969711 | TTTAGCTAAGCGGGA[C/T]AGACAGCTGGGCTGA | 51317 |
rs577198454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45982306 | TCTTTTCAGACAACT[A/G]AAATATCATATAAAG | 51317 |
rs577217878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46067173 | GGGATTTCTGTACTA[C/T]GTTGTCCTGTAAGGG | 51317 |
rs577219482 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45929222 | GGCAAGCACCCCCCC[A/G]CCCCCCACCCCCAGA | 51317 |
rs577254411 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46035270 | CCTGAAAAAAATCCA[C/T]CTTTCTCTACTGATC | 51317 |
rs577266649 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46096561 | TTCTTCCTCCTCAAA[A/T]TTTTTTTTCTCTTGA | 51317 |
rs577285619 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46027026 | ATTAAAAGTCTGAGA[A/G]CAGGAACACACACGC | 51317 |
rs577304671 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46097896 | ATCCTAGATCAGGAT[A/G]ACACATAAAACTTCA | 51317 |
rs577322372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45970657 | AATATTTTTAAAGTG[C/T]CTCAACTAACTCCAG | 51317 |
rs577339508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46107710 | AAATTACAACAGTGA[A/G]TTATCACTAATAATC | 51317 |
rs577377233 | snp | A/G | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46116451 | TATAGAAGAATCAGG[A/G]AACTTACATACTCAC | 51317 |
rs577397436 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46052499 | CATTCAACCTCACTG[A/C]CTATCAGTTTTCTGA | 51317 |
rs577402961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45934519 | ACAAACCGGCAGAGC[C/T]GCCATCAGACTTCCA | 51317 |
rs577431618 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45994761 | CTCTGCAACCCAGCT[C/T]GCTTAGCTTACCCTT | 51317 |
rs577438075 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46048768 | GAGCAAGACTCCATC[C/T]CAAAAAAAAAATAAT | 51317 |
rs577440545 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45931283 | TAAGTTAGGTGTTGT[A/G]TGGCAACCCCCAGAT | 51317 |
rs577450724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45990881 | GAACCTACACTGACA[C/T]CTCAATACTGTCGAA | 51317 |
rs577458526 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46032046 | AAAGCCCAACTCTTA[A/C]GTGCTGCTTTAAAAA | 51317 |
rs577475483 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:46047973 | ATATGTAATACTTTT[C/T]TAAACAGATTTATTG | 51317 |
rs577485129 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45999458 | AGTATATACTTCCAC[C/T]AGGTTCTATTCTTTA | 51317 |
rs577496419 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46013851 | ACGAAAGATGAAAAA[C/T]GGTAAACCAGCTTGC | 51317 |
rs577498327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46095489 | GAGTAAATGAAATTA[C/T]TTTTGCTTTTAGAGG | 51317 |
rs577531822 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45978541 | CAGTGAACAGCCAAC[A/T]GAACTATACTCTTTT | 51317 |
rs577548169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46037577 | ATCCGGGAGCCGCCT[C/T]TGTTGCGGTGAGCCG | 51317 |
rs577576142 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46047626 | TAAGAGTCTGAAAGA[C/T]ATTATTTTTTCTTTG | 51317 |
rs577577700 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46010830 | TGGACTGAGGATAAT[-/A]AATGATCAGTTCATT | 51317 |
rs577594516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45978003 | TTAGTTTTCTCTTCT[A/G]AAAAACAGAGATGGT | 51317 |
rs577685032 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46013768 | TACTGAATACCATAG[A/G]TAACAATGGTAAGTA | 51317 |
rs577685940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46060907 | ATGTCCTGAATGGTA[C/T]TGCTGAGGTTATCTA | 51317 |
rs577686011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46051595 | CTTCTTGTCTACACA[A/G]GAAAAACTGAGTTCT | 51317 |
rs577708274 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46081890 | GACAGAAACCATAAA[C/T]TACCCACAAAGCCAG | 51317 |
rs577752096 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46004590 | TTCTTCAACATAAAA[A/G]TTTTAAAGAACTGTG | 51317 |
rs577752536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45943470 | ACAGGCGTGAGCCAC[C/T]GTGCCTGCCCATCAT | 51317 |
rs577771826 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46020775 | ATGGTTGAAAAACAT[A/T]ATTCTTAAACTAAGC | 51317 |
rs577777346 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46112589 | CTCAGACTACATTTT[C/T]AAGTATTAAATTTAC | 51317 |
rs577797100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46034405 | AATAAGGTTTCTCTT[C/T]TTTCTTTTATCCTCT | 51317 |
rs577812607 | in-del | -/CTTTATCA | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46083536 | AGTCAATGCATCATC[-/CTTTATCA]CTTTTGAGTACCAAG | 51317 |
rs577817132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46044710 | CAATTAGGAAATAAA[A/G]TTCCTTTTAAGGAAA | 51317 |
rs577824357 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46036406 | TTCAAAGTTTCCTTG[C/G]CTACATCTGGGTGAA | 51317 |
rs577847383 | in-del | -/A | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46094265 | CAATCCTGAACTGAT[-/A]AAAGAATTTTGCCAT | 51317 |
rs577874192 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45984288 | CCAACATGCCAGGCC[C/T]CCAGAACTGCTAGTA | 51317 |
rs577887736 | in-del | -/TTC | | | intron-variant | PHF21A | GRCh38.p7 | 11:45977832 | GCTTTTTTCTTTTTT[-/TTC]TTCTTCTTCTTTTTT | 51317 |
rs577911909 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46044115 | TAAAATTGACTAGAA[A/G/T]CAAGTTTCAACCTAA | 51317 |
rs577922850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45994788 | CCTTCAGATGTTCCA[A/G]TAGTAGGACGACTTT | 51317 |
rs577928429 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45975009 | GCCAAATATGAAGTA[G/T]TGATTTAAAACAGAT | 51317 |
rs577959663 | in-del | -/AAG | 0.00795532 | 0.062565 | intron-variant | PHF21A | GRCh38.p7 | 11:46074133 | ATGCAAAAAAAAAAA[-/AAG]TTGTCAGATGCAACT | 51317 |
rs577967605 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46068907 | TCTGCCATACTCAGG[G/T]AAAATGCCCTATAAT | 51317 |
rs577986312 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46018723 | CACATTTTTTTTTTT[A/T]AATTCAAGAAAACAG | 51317 |
rs577995725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46076922 | ATGATGAAGCAACCC[A/G]AAGCATTTAGCCAAT | 51317 |
rs577998258 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45981733 | AAACCATAAGAGCCA[C/G]GTTAATTCTCAAATG | 51317 |
rs578000569 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45951660 | GTTCTTTTGATGAAG[A/C]AGTGTGTGGACTGAT | 51317 |
rs578025855 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46016290 | ATCACCATGTCATTT[C/T]ATGACTCAAAATTTC | 51317 |
rs578030913 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PHF21A | GRCh38.p7 | 11:46111654 | TCAAACTAAGACATA[C/T]ACATTGCAGCTTACA | 51317 |
rs578031288 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45970365 | TTCTCTAAGGATTCC[A/T]GGATAAGCGGTGAAC | 51317 |
rs578032617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46011871 | ACAACAAAACAAAAA[A/G]AGCAAAAACTTCTTT | 51317 |
rs578050711 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46104556 | CATTAGATAACACTT[A/T]TATCATCTATACTCT | 51317 |
rs578055774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45960326 | GAATGAATAAACACA[C/T]TGTGGTATATACATG | 51317 |
rs578058945 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PHF21A | GRCh38.p7 | 11:45950868 | ACTAGGTCAGTTTCT[C/T]ACATTTATACTGCCA | 51317 |
rs578075334 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46011399 | GAGGCTGAGGCAGGA[C/G]AATCGCCTGAGCCCA | 51317 |
rs578098054 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45976286 | ACCCTCCTTGACAAG[C/T]ACTTTCTGATCCCTC | 51317 |
rs578145671 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45984790 | GTGCTGCAAGTCTCT[G/T]CTTTTTCACACATTC | 51317 |
rs578152697 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46018266 | AAAAAAAAAAAAAAA[A/T]AATGTGTCCTATGCT | 51317 |
rs578156087 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46120247 | TTTTCCAAAAAAAAA[A/T]TTTTTTTAATTAAAT | 51317 |
rs578171784 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | PHF21A | GRCh38.p7 | 11:45949310 | GTACAATCAGGGTGC[G/T]GCTCTTCAGCAGGTT | 51317 |
rs578175940 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45944223 | TGTACCTACATAAGA[C/G]AGTATCTTTGCTCTT | 51317 |
rs578188757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46085483 | TTTCTTTTCTTGAAT[A/G]TGGCCTTAGACATGA | 51317 |
rs578189799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45976989 | TTGGCAAAATCAATT[A/G]AATATGTCAGGTGGG | 51317 |
rs578189874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46094435 | AAGAGCTTATGGGCC[C/T]GAGATTCCTTGGCTG | 51317 |
rs578197167 | snp | A/C/G | 0.00012251 | 0.00782569 | intron-variant | PHF21A | GRCh38.p7 | 11:45938108 | TTCCTCCTGATGGCC[A/C/G]TGTCTTTGTCCTCCT | 51317 |
rs578213551 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45939661 | GTCTCTCTACCACCC[C/G]CATCACAGTGATAGT | 51317 |
rs578237361 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46093267 | AAACTACATGTCTTC[C/T]TTTTGCCTTAAATAT | 51317 |
rs578251496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45967777 | TGACTGAACTTAAAA[C/T]GACCCTGTGGTGGGT | 51317 |
rs578255942 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46086292 | CCCGGCTAATTTTTT[G/T]GTATTTTTAGTAGAG | 51317 |
rs745335430 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46024964 | CCCTTCCAATAAATA[A/C]TTTCTCACAGGAAGC | 51317 |
rs745340322 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46105050 | ACTTCTACTAGTTTA[C/T]ACATTAACTCACTTA | 51317 |
rs745350747 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45951992 | TTGTATTTTTAGTAG[A/G]GACAGAGTTTCACCA | 51317 |
rs745360757 | snp | A/G | 0.000185615 | 0.00963187 | intron-variant, downstream-variant-500B | PHF21A | GRCh38.p7 | 11:45935109 | GGACAGGCCGGGCTG[A/G]GCAGTACTTACTTCC | 51317 |
rs745376797 | snp | A/C | 1.65444e-05 | 0.00287609 | utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:46084233 | ATCCTCTACCTTCTC[A/C]ACTTTCTCTGCTAAT | 51317 |
rs745377606 | snp | C/T | 1.64749e-05 | 0.00287005 | intron-variant | PHF21A | GRCh38.p7 | 11:45948852 | ACAAAGCAAAAGCAA[C/T]AGCAGCAAGGGAGAG | 51317 |
rs745384686 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46091547 | GCTAAAAATGTACTA[A/T]CAGACATGAAGCTAA | 51317 |
rs745415453 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46053610 | CTAACCTTAATCAGT[A/G]TTTCATACAGGCTGA | 51317 |
rs745424724 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46024302 | CCTCCCTCTCTCCCT[A/C]TATCTCTTTCCTCTG | 51317 |
rs745439893 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46002228 | CATCATTATAATCTG[A/G]CACACTGGGCTAGGT | 51317 |
rs745465926 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45947552 | CTGGAAGGGGAAGAA[A/C]AAGATGAATGCTCTC | 51317 |
rs745469384 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45948910 | GGGTCCCAGGGTGCA[C/T]TGTGCTGTTTAGGTA | 51317 |
rs745471544 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46106055 | AAGGTACTGAGAACC[C/T]GACACAATGAAAACA | 51317 |
rs745505026 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46052043 | ATAGTCAATAGTCAA[A/G]GTTGAGATGATCCAG | 51317 |
rs745505868 | in-del | -/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46007332 | TCTTTTTTTTTTTTT[-/C]CGAGATGGAGTTTCA | 51317 |
rs745512090 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46000726 | GGAGTTAGAGACCAG[A/C]CTGGCCAATAGGGTG | 51317 |
rs745533950 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46054452 | ATCCACTTACCTACT[C/T]CTACACATCTTTTTA | 51317 |
rs745538665 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45964748 | GCCTCGTTTTTTAAG[A/G]TAAAATCTGACTTCA | 51317 |
rs745588125 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46066324 | ATATTTGAGCCATAT[A/G]TACATACATATAAAT | 51317 |
rs745624063 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46015840 | CTATGGTAACAATGC[C/T]TTCGTCTGAAATACC | 51317 |
rs745631038 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45978521 | ACCAGTCCAATGTCC[A/G]TAAACAGTGAACAGC | 51317 |
rs745657760 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45962297 | AGAGAACGTTGGATA[C/T]GGGTTTGGTAACTGT | 51317 |
rs745674353 | snp | A/G | 1.64784e-05 | 0.00287035 | missense, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45971300 | GAGGCAGGCATGGTC[A/G]CAGTTGCTGCTTTCA | 51317 |
rs745724811 | snp | A/G | 1.64982e-05 | 0.00287208 | intron-variant | PHF21A | GRCh38.p7 | 11:45936475 | GCTTACAAAAAAGTG[A/G]GTATGGATAACTCCT | 51317 |
rs745743497 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45977422 | GATTACAGGCGTGTG[A/C]CACTGTGCCTAGCCT | 51317 |
rs745755115 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45956258 | ATAAAGCTAACTAGA[A/T]GAATAAATATAAAAG | 51317 |
rs745781685 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46097219 | TAAGCTTTTCAAAAT[A/C]CAAGACAGATCTTGT | 51317 |
rs745808864 | in-del | -/ATGAT | | | intron-variant | PHF21A | GRCh38.p7 | 11:46071789 | TAGTTTTAAAAAATC[-/ATGAT]ATAGCCAATTATGCT | 51317 |
rs745815546 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45993728 | AACAGAGTCAGGCTG[C/T]TGAGATCCAAGGAAG | 51317 |
rs745843157 | snp | A/T | 1.65307e-05 | 0.0028749 | synonymous-codon, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45971140 | TGTGTTTTTTGCCAC[A/T]ATTTGGACAGCCTCT | 51317 |
rs745867655 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46096337 | TCTAGTTATTGTCCC[C/T]GTCTAGGCTCACGTT | 51317 |
rs745881806 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46055758 | TTTACCTTTAAGGCA[A/T]TTATAAGTTACATAG | 51317 |
rs745903021 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46070778 | AACCAAAAGATAATT[C/T]ATGGAATACTACAAT | 51317 |
rs745988015 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46035005 | GAAGTGGAGAACATA[C/T]GATATAAATGAAAGA | 51317 |
rs745993847 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46019814 | CAACACAGAAGCAAG[C/T]AAGAAATATTACATC | 51317 |
rs746010263 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46107146 | AAATCTCATCCTTTT[-/A]AAAAATTTCAAATTT | 51317 |
rs746015868 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45946618 | CTGACCTCATGATCC[A/G]CCCATCTTGGCCTCC | 51317 |
rs746018428 | snp | C/T | 0.000159599 | 0.00893163 | downstream-variant-500B, utr-variant-3-prime, synonymous-codon | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45928906 | GGGCAACCTGCCCTC[C/T]GCCATCCCTGCTATT | 51317 |
rs746029081 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45943533 | TAACTGGTCTTCCTG[C/T]TTCCATCCTATTTTC | 51317 |
rs746051704 | in-del | -/AA | | | intron-variant | PHF21A | GRCh38.p7 | 11:45935742 | TCTTCTTCTTTTGCT[-/AA]AAAAAAAAAAAAAAA | 51317 |
rs746069068 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45941801 | CTAGGCGCTGAGGAC[A/G]TATGTTTTTAGGAAG | 51317 |
rs746075865 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46048392 | TGTATGGATATACCA[A/C]ACTTTATTTAACTAT | 51317 |
rs746094473 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46098013 | CCCAAAAGATTCTAA[C/T]AGGGAGCCAGGATTA | 51317 |
rs746103000 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46033461 | GTAGAGATGGGTTTC[A/G]CCATGTTGCCTAGGC | 51317 |
rs746103665 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45997766 | GTGCTGCTTGTCTCA[C/T]GGTGCAAATCAACCT | 51317 |
rs746144377 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45941931 | CACGGTACATCCAGA[G/T]GATTAGTGTCTGGTA | 51317 |
rs746172270 | snp | C/T | | | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45929566 | CCTCTGGCCTGCCCG[C/T]CCCATCCCGCCTGAC | 51317 |
rs746187320 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46046928 | ATATTCAGAAGTCTG[A/G]GCTGTTTGTTTGCTA | 51317 |
rs746200094 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45996910 | ACTAACTTACTTTCT[C/T]TGGGCACAAATGTAT | 51317 |
rs746203521 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46011606 | TCCCACTTGGTGGTA[C/T]TAAGCACTGCTTTTC | 51317 |
rs746206214 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45969278 | GGAAGAACACTCTCA[-/G]GGAGAGTATGGTCAT | 51317 |
rs746215204 | in-del | -/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46080166 | TTTATCTAACTACTA[-/C]GTTTTTTTTTGAGAC | 51317 |
rs746225494 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45958616 | GTCTCCAAAAAATAA[C/T]GAAAAAAATTAAATT | 51317 |
rs746251313 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46062331 | TCTCAGAACTTTTAT[G/T]AGCCAGGCATGAGAC | 51317 |
rs746311227 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45973427 | TATTTTTCTGCCTTA[A/T]GCGCATATACACATA | 51317 |
rs746331941 | snp | C/T | 1.65321e-05 | 0.00287502 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45965431 | ACGTTTTGGCTATGG[C/T]TGCAGTCTGCCCATT | 51317 |
rs746342972 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46076030 | AGAGGGAGAGTGGTG[G/T]GGAAGAAACAAGAAA | 51317 |
rs746360498 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46083051 | TTTTTATCACTTGCC[A/C]TTCAGCCAAACTGGG | 51317 |
rs746367986 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46026441 | TGCATAAACAGGTGT[A/C]AAGGTTATTTTTATT | 51317 |
rs746377849 | snp | G/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45932338 | ATCTGAGAAGACCAC[G/T]GGTAGGGCCCTGATA | 51317 |
rs746387842 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46115775 | AATTCCTTCCCTTCT[A/C]TGTTTGAATAGTAAT | 51317 |
rs746414312 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46034305 | ATGTAAGACTAATAA[C/T]CCTTTGTCACACATG | 51317 |
rs746415376 | snp | A/C | | | utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:46092212 | CTGGCTCTCCTTCAG[A/C]TCTCTAGCCCCCTAT | 51317 |
rs746430461 | snp | G/T | 1.68261e-05 | 0.00290048 | missense, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45938159 | CCACCCACAGTACCT[G/T]GTCCTGACATCTGGG | 51317 |
rs746468813 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46027237 | ACAAGTTTTCTCCGT[A/G]CTAACAGGTACAACA | 51317 |
rs746477379 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46010890 | AGTAACCAGGCAGTG[A/G]ACAGCATCATACCAG | 51317 |
rs746494964 | snp | C/T | 3.62851e-05 | 0.00425925 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45965549 | CTGAGGAGCTGCGAG[C/T]ATGGGAGGTGGTGCT | 51317 |
rs746503723 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46074459 | AGTGGCTCTTTTGGC[-/G]GGAGGGGGGAAGGCA | 51317 |
rs746512195 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46115370 | TTTACAAAAGATAAC[A/T]ATTCAAAAATTTAAC | 51317 |
rs746539829 | in-del | -/TC | | | intron-variant | PHF21A | GRCh38.p7 | 11:45977842 | TTTTTTTCTTCTTCT[-/TC]TTTTTTTTTTTTTGG | 51317 |
rs746556693 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46026647 | TGCAAAAAAAAAATC[C/T]TTTAAAGTCAAGCAG | 51317 |
rs746585345 | in-del | -/T | | | downstream-variant-500B, utr-variant-3-prime | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45929042 | CCAGTTTGGGGCTGG[-/T]TTCCCCCATCTTGAA | 51317 |
rs746592609 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45990100 | CTAATTACAAAATCT[A/G]ATCCACAAATTTCTA | 51317 |
rs746604197 | snp | C/T | 0.000185649 | 0.00963277 | intron-variant, missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45935207 | GTGTGGAAGAAAGAG[C/T]GAGGGAGGGCCGTAC | 51317 |
rs746649405 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46092442 | TGCTACTTTTCCATA[A/G]TTTTTCAAGACAAGC | 51317 |
rs746660583 | snp | A/G | 1.76362e-05 | 0.00296948 | intron-variant | PHF21A | GRCh38.p7 | 11:45935572 | CACGTACTGTTACGT[A/G]TATTGGAAAGGCCTA | 51317 |
rs746675231 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46082357 | GCCTAGTAACCAACA[C/T]CCCTACCTTGATGTC | 51317 |
rs746680502 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45988220 | CTAGAAGAGGTAAAT[A/G]TAACAGATTATTTAA | 51317 |
rs746680750 | snp | A/G | 0.000362337 | 0.013455 | synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45949426 | AAAGACTGCTCCACT[A/G]TAGACCGGATTTGCT | 51317 |
rs746705661 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46091600 | AATGTAAATAAACAC[A/G]AGTCCCAAATTTCAA | 51317 |
rs746727567 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46111657 | AACTAAGACATATAC[A/G]TTGCAGCTTACACTT | 51317 |
rs746764129 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46002427 | TTTATTAACTTTCCA[A/G]TAATAACCTACCATA | 51317 |
rs746785799 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45966057 | TCCTTTGTGGGCTTA[C/G]TCTTCCTCTGCCTCA | 51317 |
rs746790251 | in-del | -/CACG/CG | | | intron-variant | PHF21A | GRCh38.p7 | 11:46114103 | ACACACACACACACA[-/CACG/CG]CGCACACATCCCCAC | 51317 |
rs746806460 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45947814 | AAAATAACTTAGAGT[A/T]CTGGTTACTGTGGCC | 51317 |
rs746812359 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46106364 | AGCAATAATTACAAT[A/G]TGTTTTGCATATAGA | 51317 |
rs746838446 | in-del | -/AAA | | | intron-variant | PHF21A | GRCh38.p7 | 11:46118418 | CAAAAGTCTGATGTT[-/AAA]AAAAAAAAAAAAAAA | 51317 |
rs746842845 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45929826 | GGGCCAGAAGACTGC[C/T]CAGGGCTGCCCACTC | 51317 |
rs746855865 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46052274 | ACCTCTGCCAGTACA[C/G]GACAGCCTGTAAGCA | 51317 |
rs746862003 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46071162 | GGCTTCTTTTGGCTA[A/G]TGAGATGTTAACAAA | 51317 |
rs746877812 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45964916 | TGAAATCCCTTTCCC[G/T]GTTTTGTTTATTCTT | 51317 |
rs746881137 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46038953 | GCACTATCAAAGAGC[-/T]TTCCAAGCAGAGAAA | 51317 |
rs746891776 | snp | C/G | 1.64887e-05 | 0.00287125 | synonymous-codon, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45971320 | TGCTGCTTTCAAGAC[C/G]AGAGGTAGTGTCTTT | 51317 |
rs746929503 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46066661 | CTATGATTGTACCAC[C/T]GCACACCAGCTTGGG | 51317 |
rs746949874 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46104674 | CTGTAATAATAACAA[C/T]AATAATGATAAGAGC | 51317 |
rs746954794 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46020594 | ATAAAATACTATCCT[C/T]TTCGGTCCTATTTAG | 51317 |
rs746958645 | snp | A/G | 1.64735e-05 | 0.00286993 | intron-variant | PHF21A | GRCh38.p7 | 11:45948965 | TGAGGGTTGAAGGAG[A/G]AAAGGTGACTGTTGA | 51317 |
rs746979794 | snp | G/T | 1.64784e-05 | 0.00287035 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45979787 | CAGGTTGGGAGAGGC[G/T]GCAGCTGACTGCTGG | 51317 |
rs746984909 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45996485 | CCTTGACAGTGGCCA[A/C]ATAAATGATTTCCCT | 51317 |
rs746994891 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45940003 | ACAAGAAGCAATAAT[A/G]GAGAGGAATGTGAAT | 51317 |
rs747004808 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46081031 | CCTGCTGTGTGGTAC[A/G]CTCACTGGACTAATT | 51317 |
rs747007817 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46042358 | AACCAGAAGATCCTA[A/G]AAGCAGCCATATTAG | 51317 |
rs747048795 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45952741 | TTTGATGGCTTTATG[A/C]CACTATTTCACATGG | 51317 |
rs747062825 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45941122 | AATTTTTTTTGAGAC[C/T]GGGTCTGGCTCTGTC | 51317 |
rs747063276 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45937043 | CTAAAGTATAATCTA[A/G]ACCCTATGTCAAAAA | 51317 |
rs747077675 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46058072 | CAACTTTTAACAAAG[C/T]CTTGTTAAATGTGAA | 51317 |
rs747104694 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46072378 | AGGGCTTGCTCTTTG[C/T]TGCTTCTCCCCCTTC | 51317 |
rs747106223 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46023526 | GTGTCATATGGAATA[C/T]TGGTATCCCCTCAGA | 51317 |
rs747133270 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46006008 | GCACAATTTTAAACT[C/T]TGAAAATGGGCTGGT | 51317 |
rs747168429 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45968397 | ACCTCAACTCTAACT[A/C]ACTCTAGCCTGCATG | 51317 |
rs747169788 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46013859 | TGAAAAACGGTAAAC[A/C]AGCTTGCAGGACTGG | 51317 |
rs747183580 | snp | A/C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46094362 | ATAGAAAATCAAACC[A/C/T]GGAAAAGTTAAGTGA | 51317 |
rs747186526 | snp | A/C | 1.65127e-05 | 0.00287334 | intron-variant | PHF21A | GRCh38.p7 | 11:46076733 | ACGTTAAAAATATGC[A/C]CCCCTCCCCTTTTCC | 51317 |
rs747188891 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46036078 | CTAAAGTAGTGCTTA[C/T]GGAAAGAAGATAGAT | 51317 |
rs747189325 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46109317 | CTAAATAAGATCCTA[C/T]GTGTAAAAAGGCTTA | 51317 |
rs747248838 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46021651 | GGCTCAAGCGATCCT[C/G]CTGCCTCAGCCTCTC | 51317 |
rs747258401 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45983880 | GGTTCTCACTGCTCC[C/G]TATATAAAGGATATC | 51317 |
rs747272820 | snp | C/G | 1.65329e-05 | 0.0028751 | synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45953554 | CTCCCGTTTTGGTTT[C/G]GGTGCAGCAGGTGGG | 51317 |
rs747279054 | in-del | -/CG | | | intron-variant | PHF21A | GRCh38.p7 | 11:46040931 | ACACACACACACACA[-/CG]CACGCACGCACAATT | 51317 |
rs747288742 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46069703 | ATCTGGATTCTAGTA[C/T]TGAATCTCATACTGA | 51317 |
rs747292441 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46087185 | ATATGCACATCTTTT[C/T]AAACAAGAAGACATT | 51317 |
rs747337419 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46115043 | AAGGCAGAAAACATT[C/T]CTGTAACTGATTCCA | 51317 |
rs747338557 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46035132 | CCTCCCAATATGTCC[C/G]CTCTCTTTTTGGCTT | 51317 |
rs747382214 | snp | C/T | | | synonymous-codon, missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934151 | GATGAGGCGAATCAG[C/T]TGTTTTACCTTCTCC | 51317 |
rs747392354 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45998002 | GATGGCAGCACAGTT[C/T]TGCTCCTATCAAAAC | 51317 |
rs747461992 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45942258 | AGAAGCTCTTAGTTT[G/T]TGAGTTGATGAGTGG | 51317 |
rs747487755 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46063182 | ATGAATTGAATTCGC[C/G]GGGGGGGCTGGCATG | 51317 |
rs747498734 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45974940 | GGCAAATACTGCCAA[C/T]AGCAAAATCCTTTTT | 51317 |
rs747531028 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46077271 | TCTCCCTTATTTAGC[A/G]AAGTACATTTGTTAT | 51317 |
rs747548124 | snp | C/T | 1.65463e-05 | 0.00287626 | missense, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45945934 | TCAGGGGAGTCAGGA[C/T]GACTGGATTGGGGGG | 51317 |
rs747555644 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46064853 | GATTTACCCTTCTAA[C/T]AATGTATTGCTTTGG | 51317 |
rs747596415 | snp | C/G | 1.65427e-05 | 0.00287595 | missense, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45945944 | CAGGATGACTGGATT[C/G]GGGGGATGTTGGGGT | 51317 |
rs747624336 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46049071 | CTGACAACAGGGATG[A/T]CAATGCTTCACACCA | 51317 |
rs747643238 | snp | C/T | | | intron-variant, utr-variant-5-prime | PHF21A | GRCh38.p7 | 11:46118026 | CAAAAATTTCCTTTA[C/T]CTTGCTGTAGCACCT | 51317 |
rs747651885 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46082096 | CATCACAGGACATTA[C/T]TATTTAAATATTTAC | 51317 |
rs747679553 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45960499 | ACAGGTACATCTATG[C/G]AGACAGAAAGCAGAC | 51317 |
rs747705161 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46012108 | TGTTCATTACTACCG[A/G]AAAGAATCCTTCAAC | 51317 |
rs747712458 | in-del | -/AA | | | intron-variant | PHF21A | GRCh38.p7 | 11:45963421 | GTAAAACTCTGTGTC[-/AA]AAAAAAAAAAAAAAA | 51317 |
rs747759245 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46116539 | GGACATACAATTCAC[A/G]GGATCTTCAAAAGGG | 51317 |
rs747767765 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46076032 | AGGGAGAGTGGTGGG[A/G]AAGAAACAAGAAAAC | 51317 |
rs747784708 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46077479 | AATTCCAAAATTAAA[A/G]TTTTCAAATGCTTAA | 51317 |
rs747832010 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46042223 | CTGTGGGAAAGCCAC[A/G]TGACAAAACATATTC | 51317 |
rs747837928 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45994762 | TCTGCAACCCAGCTC[A/G]CTTAGCTTACCCTTC | 51317 |
rs747848679 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:45974565 | TCAAGTAATCCTCCC[-/A]ATCTCATTCTCCTGA | 51317 |
rs747867959 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46005325 | TAAAATTTATACAAA[C/T]TTATGCTTGGGACCA | 51317 |
rs747878768 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46076304 | ATTAACATAAAGGCA[A/T]GACCATACTTAGAAT | 51317 |
rs747897147 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45931397 | CAACTAGTCCAGGCA[C/T]CTCCAAGGCTCCCTG | 51317 |
rs747910695 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46108980 | CCATCCCATTCCAAT[A/G]TTTACTATTTTCAAA | 51317 |
rs747925695 | snp | C/T | 0.000182963 | 0.00956284 | intron-variant | PHF21A | GRCh38.p7 | 11:45935598 | GCCTAGGTCTCTGCA[C/T]CTATGTATCGACTGC | 51317 |
rs747948585 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45950481 | GAAGAAGAATTGTCT[C/T]GAGCCACACATAAAA | 51317 |
rs747967917 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46055457 | CCACCAGAACTGGCA[C/T]TCAGAATGAGGAGTG | 51317 |
rs747971329 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46093116 | TGTTTCTATGCCACA[C/T]ATCTAATCAGTGATG | 51317 |
rs747976600 | snp | C/T | 1.64776e-05 | 0.00287028 | missense, utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45979944 | ACTATCAGGTTCTTC[C/T]GTAGCTGTTCAACTA | 51317 |
rs747997908 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46101481 | GGGAATAGGTACGTG[A/G]GGTTATATTATTCAC | 51317 |
rs748015069 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46017791 | CCCCTAGAAATAAAC[A/C]AAGGTTCCACAGAAA | 51317 |
rs748023209 | in-del | -/AA | 0.000117331 | 0.00765843 | intron-variant | PHF21A | GRCh38.p7 | 11:46076848 | AAAAATATCTGTGAG[-/AA]AGATATTTCATTTGT | 51317 |
rs748036764 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45966966 | ACCCTGTGGGCAAAA[C/T]GCTTTCCCCTTATGC | 51317 |
rs748036823 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45949645 | CTACTGGAAGCAAAT[A/G]TGTAGGACCATCTAC | 51317 |
rs748037044 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46004406 | AGGAAATGGATTTCA[C/T]TTTTAATAGATAAGA | 51317 |
rs748037205 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45983136 | GCTAGAGCAAGGTGA[C/T]GACCAATCAGAACCA | 51317 |
rs748038572 | snp | C/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45949448 | GGATTTGCTGTTGTT[C/G]TTCTTTTTCGCTCTT | 51317 |
rs748053968 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46054281 | TGAAAATTATATCAC[A/T]TAAAGTTTCTTCTCT | 51317 |
rs748084478 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45938731 | GAATGAGGTCTATCT[A/T]CTTTTTTCTTTCTCA | 51317 |
rs748123143 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46019765 | CTTGACAGTTAAACA[A/G]TAGCTCTGCTCTAAA | 51317 |
rs748150404 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45994992 | CCACAGAAATGTGTA[C/T]AATCTCTGTGCTATA | 51317 |
rs748201292 | snp | G/T | 1.70504e-05 | 0.00291975 | intron-variant | PHF21A | GRCh38.p7 | 11:45938136 | CCTCGGCCCCTCCCC[G/T]GTTGGACCCACCCAC | 51317 |
rs748229248 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45975937 | AATATATGCCATATA[C/T]AACCTCCCATTCGTC | 51317 |
rs748229702 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46097463 | CTTTTCCTCCAAATA[C/T]CTTCATGGCTCACTC | 51317 |
rs748256179 | in-del | -/AA | | | intron-variant | PHF21A | GRCh38.p7 | 11:45939773 | GGAGAACATAGCCCA[-/AA]AAAAAAAAAAAAAAA | 51317 |
rs748263265 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46060902 | TGCTTATGTCCTGAA[C/T]GGTATTGCTGAGGTT | 51317 |
rs748267423 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46043652 | AAAAAAACTGACCCA[C/T]TTTTAGAAGTCAGCA | 51317 |
rs748269103 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46113244 | GCAAGTTTCAAGAAA[A/G]TCTGAACTATCTAGC | 51317 |
rs748296198 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46009567 | ACGCTATGTATTACA[C/T]AATTTAATCTTCAAA | 51317 |
rs748307571 | snp | A/G | 2.08535e-05 | 0.00322898 | intron-variant | PHF21A | GRCh38.p7 | 11:45965295 | CTACTGCCCAGAGCA[A/G]GTACATACTCTGCCT | 51317 |
rs748311500 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45954439 | CAGAACCACCCTTAC[A/G]TGGAATATTAAAAAT | 51317 |
rs748319823 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46096436 | CACAACCCATTAGGG[C/T]CTTTGCCTCCCTCCA | 51317 |
rs748320509 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46073327 | GCGAGACCCCGTCTC[-/A]AAAAAAAAAAAAAAA | 51317 |
rs748321099 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45993782 | GAAAGGGCCAAGCAG[C/G]AGAGGAGCCAGTGGA | 51317 |
rs748376763 | snp | C/T | | | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46119559 | CCCTCATCACAACAA[C/T]TCAACTACTTAGAAA | 51317 |
rs748397500 | snp | A/G | 3.29554e-05 | 0.00405914 | synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45936510 | TGCTTTGTAGGCAAT[A/G]TAGGAATGAACAATT | 51317 |
rs748404837 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46007221 | CTAAGAGATGAGAAA[A/C]GGGCCCCCTGTCTTT | 51317 |
rs748416195 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45935401 | GAAAATCCTCTCTCT[A/G]ATTAAAGCCAAGAGG | 51317 |
rs748429647 | snp | C/T | 1.67142e-05 | 0.00289081 | synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45965375 | AGCGAGTCTGGTCCC[C/T]GGAGTAGCTATCACA | 51317 |
rs748433395 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45950173 | AAGCTGTGGGCCAGA[A/G]AAAAAGGCAGTGCCA | 51317 |
rs748436911 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45968787 | ATACAAAAATTAGCC[A/G]GGCGTGGTGGCACAT | 51317 |
rs748451265 | in-del | -/AG | | | intron-variant | PHF21A | GRCh38.p7 | 11:46083246 | CTCTGCAGCGGAACA[-/AG]AGTTTAACGAGATCC | 51317 |
rs748453075 | snp | A/G | 1.72591e-05 | 0.00293756 | intron-variant | PHF21A | GRCh38.p7 | 11:46079111 | AAATTTAACAATTAA[A/G]TGAATAACAATAGTA | 51317 |
rs748458906 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46023731 | GAGACAGAGGTGGGC[A/G]GATCGCCTGAGGTCA | 51317 |
rs748464505 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46072508 | GGAACCACTCTCAGC[A/G]GCCCTAGCCCTAGGG | 51317 |
rs748524691 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45984442 | ACAGAGCCTCTGACA[C/T]TTCAAGTCACAGTTT | 51317 |
rs748551196 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45945387 | GCAGAGTTTCTGCTC[A/G]ACAGTTTCTGATCAA | 51317 |
rs748598423 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46062166 | TCACCACGTTGTGCC[C/T]TGGTATGAGGGTGTG | 51317 |
rs748605793 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46104423 | AAAAAAGAAAAGCTT[A/G]TATCACTATGGGTTT | 51317 |
rs748610955 | snp | A/G | 1.68462e-05 | 0.00290221 | missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934032 | GAGGGGGAAGGGGCC[A/G]GCGTGGAGGTGGCGG | 51317 |
rs748638963 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45961786 | CCATTTTAGAGCGCT[A/G]GAGAGGACAAGGACA | 51317 |
rs748690004 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46051579 | CTTCAGAAACACAAA[C/G]CTTCTTGTCTACACA | 51317 |
rs748695596 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46102298 | AACTCAACATGTAAC[C/T]ATAATTAATTTCCAA | 51317 |
rs748703396 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46058521 | TATTTGCCAAATGAA[C/T]TGAGGTTTAAAACTT | 51317 |
rs748712860 | in-del | -/A/AA | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46119750 | GGTCAGGGGAAAAAA[-/A/AA]AAAAAAAAGAAATCC | 51317 |
rs748724067 | snp | A/C/G | 6.64125e-05 | 0.00576216 | missense, utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934071 | GGGGGGGTGCAGTCC[A/C/G]GGCCATTGGAGATGG | 51317 |
rs748727966 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45943969 | AACTGGCTATCTTTT[C/T]AAAAACGTCAATGTT | 51317 |
rs748739458 | snp | A/G | 0.000132411 | 0.00813559 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934094 | GGAGATGGCCCCCAC[A/G]GTGGCCTCAGAGTCT | 51317 |
rs748775163 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46036610 | AAGTAAAGGTACAGG[C/T]ATACATTTCTTGTGA | 51317 |
rs748801722 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46000309 | CTCTCACCTCTAGCT[C/G]TAACAGAAGCTAAGC | 51317 |
rs748812383 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46104566 | CACTTTTATCATCTA[C/T]ACTCTTTCTCACCAC | 51317 |
rs748829548 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46066097 | ATAGTCTCATAAACA[C/T]GTTGAACAAAATAAG | 51317 |
rs748862496 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45999208 | ACAGAGAAGAGAGCA[A/G]TAAATAGAGAAAACA | 51317 |
rs748875715 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45962162 | AGTTTATCCACCTTA[C/T]ATATAGACATCACAT | 51317 |
rs748887148 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45990514 | ATCCACCCGCCTCAG[A/C]CTCCCAAAGTGCTGG | 51317 |
rs748887452 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46015510 | CAATAATAAATTAAC[C/T]TTAGCTTAGTGTAAT | 51317 |
rs748890877 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46028650 | ATGATCTCGGCTCAC[G/T]GCAACCTCCGCCTCC | 51317 |
rs748891753 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45956771 | TGAAGAACAAAAAAC[A/G]TAAGATATACAGAAA | 51317 |
rs748900403 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46102518 | TCAAAATATTTTAGC[A/C]ATTCACAACACCAAA | 51317 |
rs748917561 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46065086 | CAGACATTGTTAACT[G/T]TCTTGAATATCCATT | 51317 |
rs748967157 | in-del | -/AAAAC | | | intron-variant | PHF21A | GRCh38.p7 | 11:45975377 | AAAATAAAATAAAAT[-/AAAAC]AAAACAAAACAAAAT | 51317 |
rs748978929 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46025035 | TCTTAATCTTGTCAT[G/T]AACACTATTAGCCAG | 51317 |
rs748979964 | snp | A/C | 1.64741e-05 | 0.00286998 | missense, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45971270 | ATAGCAATGGTAGGT[A/C]TCTGGCCCACCACAG | 51317 |
rs748984095 | snp | C/T | 1.65559e-05 | 0.00287709 | intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45946069 | GGGGGAAAATGATCT[C/T]ACATACCTTTGGCCA | 51317 |
rs749043938 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46096043 | CTTCCTAACTTCCAA[C/T]AGAAAGCAAGTAAGT | 51317 |
rs749086519 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45975527 | TGTATACTCAAACAA[A/C]CACAAATAGAAACTT | 51317 |
rs749119706 | in-del | -/AAAC | | | intron-variant | PHF21A | GRCh38.p7 | 11:45962434 | TGAAATATAAATAGA[-/AAAC]AAGGATAGTTGAAAG | 51317 |
rs749123863 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46042289 | TGAACCAAACTTTAA[A/G]ATTGCTGGACAGGTA | 51317 |
rs749172917 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45972436 | CACCTTTACTGTATA[-/T]TTGCACTGTCTGATT | 51317 |
rs749173927 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45992022 | TACAAGAGAATGAAG[C/G]AGGCCAGGTGTAAGA | 51317 |
rs749181999 | snp | A/G | 3.30267e-05 | 0.00406353 | intron-variant | PHF21A | GRCh38.p7 | 11:45935612 | ACCTATGTATCGACT[A/G]CTGAAGGCATGAGGT | 51317 |
rs749202903 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46094535 | ACAATAAACACTAGC[A/G]AAATATTTTTGGAAA | 51317 |
rs749211943 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46041317 | GTCATTAACAAATGA[A/G]ATCTTATTTAGGATG | 51317 |
rs749219364 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45950920 | TGATTTTCAGGAATG[A/T]CAGCAGGTGTTTCTG | 51317 |
rs749242467 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46040705 | TTACATGAAACTGCA[C/T]ACTATGTTGGAGAGC | 51317 |
rs749244012 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46095826 | CTACTACAAATTTCA[A/G]ATGATTAAGTTTATA | 51317 |
rs749282539 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45968302 | ATGCTTTAATGAATG[A/C]CTGCTGCTCCTAGGA | 51317 |
rs749290647 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46109057 | TGATACACTGTAGCT[A/G]TGGCCATTTCAGTAA | 51317 |
rs749327931 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45941866 | GCTAAACAATTTTTA[A/T]AATTATGTTAACGTA | 51317 |
rs749330386 | snp | C/T | | | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46118850 | GAAGGAGGGGGCCAG[C/T]CTTCAAAGACCAAAA | 51317 |
rs749332340 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45966788 | GCACGCCCAGCTAAT[A/T]TTGTATTTTTAGTAC | 51317 |
rs749332432 | snp | C/G/T | 5.95544e-05 | 0.00545658 | downstream-variant-500B, utr-variant-3-prime, missense | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45928902 | ACCAGGGCAACCTGC[C/G/T]CTCCGCCATCCCTGC | 51317 |
rs749360727 | in-del | -/AATT | 1.66563e-05 | 0.0028858 | intron-variant | PHF21A | GRCh38.p7 | 11:45935780 | GGAACGGTTTTTGAC[-/AATT]AATTCTTTGAAATGT | 51317 |
rs749381550 | snp | C/T | | | missense, utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45979804 | CAGCTGACTGCTGGG[C/T]GTGGTGGTGGTGGTA | 51317 |
rs749392471 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45996676 | AAAATGAAAGGCAAT[G/T]TTGAAAGTAGGTGTT | 51317 |
rs749413512 | in-del | -/A | 1.65225e-05 | 0.00287419 | intron-variant | PHF21A | GRCh38.p7 | 11:45979981 | CTACCAAATGAAGAC[-/A]AAAAAGAAATAAAAG | 51317 |
rs749416748 | snp | C/T | 1.69548e-05 | 0.00291154 | intron-variant | PHF21A | GRCh38.p7 | 11:45938148 | CCCTGTTGGACCCAC[C/T]CACAGTACCTGGTCC | 51317 |
rs749417452 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46032223 | TATATTTTCCTATTT[A/G]TAAATGTAATATAAT | 51317 |
rs749421186 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46046818 | TCTGGACAAACGAGA[A/G]TAGTTTCCAAACACT | 51317 |
rs749428496 | in-del | -/TG | | | intron-variant | PHF21A | GRCh38.p7 | 11:46021547 | GCATGTGTGTGTGCA[-/TG]TGTGTGTGTGTTCAG | 51317 |
rs749441061 | in-del | -/TCTCTC | | | intron-variant | PHF21A | GRCh38.p7 | 11:46038115 | TTGTATACTCCTATT[-/TCTCTC]TCTCTCTCTTTTTTT | 51317 |
rs749473603 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45940397 | AACAGGGTTTCACCA[C/T]GTTGGTCAGGCTGGT | 51317 |
rs749493203 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46116280 | AAAATGATATATCCA[A/T]ATATACCTAATACTA | 51317 |
rs749507233 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46045758 | TTTTGGAAGCCCTAC[C/T]CTTGCCTTCTGTGAG | 51317 |
rs749509550 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46101860 | GTGCTGGTCTCCCTC[-/T]TTTTTTTTTTTTTTT | 51317 |
rs749528283 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46010543 | GGAATAGTGGTATGA[A/G]TAACTCAAAATTAAA | 51317 |
rs749530437 | snp | A/G | 1.89636e-05 | 0.0030792 | downstream-variant-500B, utr-variant-3-prime, synonymous-codon | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45928852 | CGAGGCTGAGGCTGG[A/G]CCGGCGCTGCCCCTC | 51317 |
rs749535040 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45995412 | AGGAATCATTCTTAC[A/G]CAGGGGTGCATACCT | 51317 |
rs749559151 | snp | A/T | 1.65334e-05 | 0.00287514 | missense, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45938294 | TGCAAACGCTGCAAA[A/T]ATCCTCATGAATATC | 51317 |
rs749564346 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46114821 | ATCAATTCCTTTCTG[A/C]TGCTCCTTCTCCTCA | 51317 |
rs749601866 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45935371 | TGTAGCTGTTACTTA[C/T]TCAGCCTGAAGACTG | 51317 |
rs749613839 | snp | A/G | 1.65611e-05 | 0.00287755 | synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45965405 | AATGCTGGTGAGCTG[A/G]GCCATGGGGAACGTT | 51317 |
rs749648099 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46059577 | ACTACACACATGCCA[C/G]CACACCTGGCTAACT | 51317 |
rs749653062 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PHF21A | GRCh38.p7 | 11:45933410 | GATACACTGTCCCAC[A/C]CCCTGCTCCCTCCAG | 51317 |
rs749655482 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45971789 | TCATTTCTATCCTAA[C/G]TGCTACAAGCTCACC | 51317 |
rs749662029 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46058241 | ATAACCTCACAACTT[C/T]CAATCATTTACTTAG | 51317 |
rs749690660 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45970341 | TATCTGGTTGAGTGA[A/C]CTCGTTGCTTCTCTA | 51317 |
rs749705930 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46024891 | TCCCTTTTCTATACC[A/G]TAGTGACTCCTAGTT | 51317 |
rs749714836 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46022650 | ATTTTTTTTTAGAGA[C/T]AAGGTCTCACTATGT | 51317 |
rs749728327 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45955263 | ATCTAAGCGAGAATC[A/T]CTCAAGTCTTTCTCT | 51317 |
rs749740019 | snp | A/G | 1.6525e-05 | 0.00287441 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934192 | GCATCTCCTTCTGCC[A/G]GGCCAGGATGGTGTT | 51317 |
rs749756234 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46038148 | TTTTTTTAAATGGAG[G/T]TTTGCTTTTTTTTTG | 51317 |
rs749761719 | snp | A/G | 1.66893e-05 | 0.00288867 | intron-variant | PHF21A | GRCh38.p7 | 11:46079121 | ATTAAATGAATAACA[A/G]TAGTAGTTTTACCTG | 51317 |
rs749765003 | in-del | -/TCCAAAT | | | intron-variant | PHF21A | GRCh38.p7 | 11:46081633 | CAACTTACTGGACCA[-/TCCAAAT]CCCTAGTAACTTTAA | 51317 |
rs749817941 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46086361 | CCTGACCTCGTGATC[C/T]GCCCGTCCTGGCCTC | 51317 |
rs749818416 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46030811 | TAAACCACATAGTGT[-/G]TGTGTGTGCGTGTGT | 51317 |
rs749831036 | in-del | -/TTT | | | intron-variant | PHF21A | GRCh38.p7 | 11:45986403 | ACTGCCTTTAATTTG[-/TTT]TGTCAAACAAGAAAG | 51317 |
rs749833352 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45985402 | CTAAGTGAAGATTTC[A/T]CCATTTTATGAACAA | 51317 |
rs749838069 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45947120 | CTCCTAACTGAGAGA[A/C]CTGATTTGTGTAAGA | 51317 |
rs749838628 | snp | C/T | 1.80445e-05 | 0.00300365 | synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45965321 | TGCCTGTACCTGTTT[C/T]TCAAGACTTGGCTTG | 51317 |
rs749861689 | snp | A/C | 8.25757e-05 | 0.00642503 | utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:46084220 | AGTCTGCAACTCCAT[A/C]CTCTACCTTCTCCAC | 51317 |
rs749898373 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45966676 | CCAGGCTGGAGTGCA[A/G]TGGCGCGACCTCGGC | 51317 |
rs749913573 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46027572 | AGTCTTTAATGCACA[C/T]AACTCTTTCAAGAAT | 51317 |
rs749923960 | snp | G/T | 1.6473e-05 | 0.00286988 | intron-variant | PHF21A | GRCh38.p7 | 11:45950165 | CAGGAACAAAGCTGT[G/T]GGCCAGAAAAAAAGG | 51317 |
rs749967548 | snp | C/T | 1.66103e-05 | 0.00288182 | intron-variant | PHF21A | GRCh38.p7 | 11:45950299 | ATGCTTCAGTCTGGG[C/T]TCTCACAAAGCCAAT | 51317 |
rs749975522 | snp | C/T | | | intron-variant, downstream-variant-500B | PHF21A | GRCh38.p7 | 11:45935060 | GGGAGAAGCCTCTGT[C/T]CCCCTGCTGCAAATA | 51317 |
rs749988281 | snp | A/G | 1.6476e-05 | 0.00287014 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45979766 | CACATTTACCTGTGA[A/G]GCAGTCAGGTTGGGA | 51317 |
rs749990087 | in-del | -/CTT | | | intron-variant | PHF21A | GRCh38.p7 | 11:46100919 | AGTCAAAAGTCCCTC[-/CTT]GACAAACCATTTTAT | 51317 |
rs749991850 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46019034 | AATAAGGCAAGAAAA[A/C]GAAAGGGGGAAGAAA | 51317 |
rs750008821 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46060073 | TATAAATTTATGGAA[C/T]AGAAAAAAAGACTTA | 51317 |
rs750025387 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46057315 | TTTCCCATCAGCCTT[A/C]CTCAGCCAGGATTCC | 51317 |
rs750037206 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46083806 | TAAAAACTTTAGTAC[A/G]TATGGTAGTTGAGTT | 51317 |
rs750041794 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45980927 | TAGGGATTTAACTGC[A/G]TGGAGTGAAAAATTA | 51317 |
rs750054339 | in-del | -/G | 0.000185684 | 0.00963366 | intron-variant, utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45935172 | CTGGTCAGGAAAACC[-/G]GGGAAATGCAATCAG | 51317 |
rs750063787 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45936092 | AGACCAGCCTGGGTG[A/T]CATGGCGAAACCTGT | 51317 |
rs750077851 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46033086 | TGTTTTATTAGTTTT[G/T]ATGTATCCTGTGACT | 51317 |
rs750081261 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46068043 | GTGTAGAGAAGAGGA[C/T]GTGTGAAGAAGGCAC | 51317 |
rs750125683 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46089004 | TCAAAACTTGACTCA[C/T]CAACCAACATTTCTT | 51317 |
rs750135704 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45997484 | TGCCAAAAGATGAAG[C/G]CAGCCCATGCCTACG | 51317 |
rs750146481 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45941617 | AAATGAATATAAAAT[C/G]CCAAAACATTTTACC | 51317 |
rs750151158 | snp | C/T | 1.64773e-05 | 0.00287026 | missense, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45938245 | TGATATACACGGGAA[C/T]ATGTGTCGCACATCA | 51317 |
rs750159691 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46099330 | AAACTCCTGCTGCAT[C/T]GATAGCCAAGAATAA | 51317 |
rs750169255 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45962618 | GAACATTGGCCAGGC[A/G]TGGTGGCTCATGCCT | 51317 |
rs750171235 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46082120 | TATTTACTGAACATC[A/T]ACTATGTGTACATTG | 51317 |
rs750181359 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46046431 | CAAACCAAACCCAAA[A/C]CAAAAAACCTTGCCA | 51317 |
rs750189790 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45939509 | AAAAAGCCAAAGCAA[A/C]AGCTGACAATGTTCT | 51317 |
rs750223230 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45957860 | GAATCTTCGAAAAGA[A/G]TAACAAAATCGACAA | 51317 |
rs750223852 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45996338 | AGTGATCTATATTAC[A/C]ATTAGATCACATTGG | 51317 |
rs750249302 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46010047 | GAAGTCTGAGGAACA[C/T]TCATTTAGTTGCTTA | 51317 |
rs750249619 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46098244 | AAAATCCACAATTCA[C/T]AGATGGGTGTAGTAA | 51317 |
rs750255245 | snp | A/G | 4.24007e-05 | 0.00460419 | downstream-variant-500B, utr-variant-3-prime, synonymous-codon | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45928876 | GCCCCTCATCTTAGC[A/G]TTGGGCAGACACCAG | 51317 |
rs750270114 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46113687 | AAAAATTAGTTGGGC[A/G]TGGTGGCGCACGCCT | 51317 |
rs750283703 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46061925 | TGTCTCTATTCTATC[C/T]CCGGACTTGATCAAG | 51317 |
rs750327073 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46060704 | TTTAAGTTCCATATA[A/G]ATGCTGGATATTAGA | 51317 |
rs750336174 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46030289 | GACAATATAAAATTA[-/T]TTTTTTCTCTCCATA | 51317 |
rs750337585 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46114473 | GGCACACAAATTTAA[C/T]GCAATCCAGCTAAAA | 51317 |
rs750397114 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45971064 | TATACTATACAAATG[C/G]GTATCCTAACCTTCT | 51317 |
rs750397205 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46008531 | GTCAAAGGTAGAAGA[C/T]GGGAAAAGAGTCTGC | 51317 |
rs750416828 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46050882 | CTCTACTATTTGCCA[G/T]AGAGGCAGCTGCTGG | 51317 |
rs750425450 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46113014 | CTTTAGAATTTGAGC[A/G]GCATAATAATCATAA | 51317 |
rs750447716 | snp | C/G | 3.32325e-05 | 0.00407617 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934061 | GGCATTGGCAGGGGG[C/G]GTGCAGTCCGGGCCA | 51317 |
rs750449728 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45988577 | GTAATAGCACAGGCA[C/T]ATAAATTTTAAAAGA | 51317 |
rs750468836 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46088508 | TAAAAAGGTCAGCCA[C/T]GGTATCTGGAAAGCA | 51317 |
rs750521494 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45944901 | CCTCCAGAGTAACTG[C/G]GATTACAGGAGCACG | 51317 |
rs750528766 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45969014 | GGTATTTACTAGGGA[-/T]TTTATCTGATAAACA | 51317 |
rs750558903 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46103331 | TAATACTATATATTT[A/G]CTATGCTAATTTTAA | 51317 |
rs750581369 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46103808 | TGATCAGTAGTGAAT[A/G]AACAAAGTTAATTAT | 51317 |
rs750584861 | snp | C/G | 1.64857e-05 | 0.00287099 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934141 | CGATGCCGTGGATGA[C/G]GCGAATCAGCTGTTT | 51317 |
rs750588120 | in-del | -/AGCAT | | | intron-variant | PHF21A | GRCh38.p7 | 11:46027082 | TATCTGATGTGTGAG[-/AGCAT]AGCACACAGCACAGC | 51317 |
rs750604074 | snp | A/G | 2.62347e-05 | 0.00362169 | intron-variant | PHF21A | GRCh38.p7 | 11:45969932 | GAAGATAAATAAACC[A/G]GAGAGAACAATTACT | 51317 |
rs750610677 | in-del | -/TGT | 1.64852e-05 | 0.00287094 | cds-indel, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45979827 | TGGTGGTACTGCTGC[-/TGT]TGTTGTAGTTGCTGT | 51317 |
rs750626470 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45961299 | GTCTGCATGAAAAAT[C/G]AAAGGTAGGCAGGTG | 51317 |
rs750633870 | in-del | -/CC | | | intron-variant | PHF21A | GRCh38.p7 | 11:45983203 | TTCACAACTGCTCCT[-/CC]CCCCCAGGGCCTGAA | 51317 |
rs750649013 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46102014 | AGGCATGTGCCACCA[C/T]GCCCAGCTAATTTTT | 51317 |
rs750681100 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46117577 | AAAAAACTACAAGAA[A/G]TCTAAAATTTTTTCA | 51317 |
rs750714275 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45960216 | CAAGTAGTCATACAA[A/G]TGCTTGCACATGAAT | 51317 |
rs750716760 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46063121 | GAGAGGAATAGAGAC[A/G]AAGAGAATAAAAAAT | 51317 |
rs750718116 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45976112 | CGTTTCGTGGATCAC[A/G]CACTCCAACCACACC | 51317 |
rs750773115 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46094825 | GAATCACTTGAACCC[A/G]GGAGGCAGAGACTGC | 51317 |
rs750789604 | in-del | -/AC | | | intron-variant | PHF21A | GRCh38.p7 | 11:46116329 | CTTTTTCACTGTGAA[-/AC]AAGCTTGAAAGCTTT | 51317 |
rs750804686 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46077139 | AAAGTATCCATTGAC[A/C]GAAAACCCAAAGCTC | 51317 |
rs750806152 | snp | C/T | 2.70544e-05 | 0.00367784 | intron-variant | PHF21A | GRCh38.p7 | 11:45965649 | TTGTATTACTTAAGC[C/T]GCTCAAGTCCTATAA | 51317 |
rs750836478 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46037339 | TAGCCTTCAGGCCTA[C/T]TGATAAAAAATGGAG | 51317 |
rs750842073 | snp | A/G | | | upstream-variant-2KB | PHF21A, LOC105376661 | GRCh38.p7 | 11:46123032 | GGGGTGGGGGGTTTT[A/G]TTTTTAAAGCTCAGC | 51317 |
rs750846220 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46027185 | CTGCTTTTTCTCCCT[A/G]ATTTTATTATATTTC | 51317 |
rs750849608 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46005732 | AGCAATGAATAAAAG[A/T]ATAATATTTGTAGCA | 51317 |
rs750863694 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46041872 | TAAATACACTAGTAG[C/T]CATTTCTATTACAAA | 51317 |
rs750875268 | in-del | -/TC | | | intron-variant | PHF21A | GRCh38.p7 | 11:46034332 | CATGTGTTAAAAATA[-/TC]TGTCTTGAATTTTTT | 51317 |
rs750909576 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46093528 | GTTCTCAGGCCCATG[C/T]AAATAACAATTTTAA | 51317 |
rs750922454 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46069726 | CATACTGATAAATTA[C/T]ACAATAATGGTTAAG | 51317 |
rs750941342 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45950125 | TCCAATTTTCTATTC[C/T]AGGAATTCAATCAAA | 51317 |
rs750960518 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46005042 | TTTAACACATGCATG[C/T]ATACACCCAACTAAT | 51317 |
rs750979227 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45936102 | GGGTGACATGGCGAA[A/G]CCTGTCTCCACCAAA | 51317 |
rs750994805 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46108387 | ACAATCAATCTAAGG[C/T]ATTAGGTTTGGAATC | 51317 |
rs751033054 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45951616 | CCTTAGAAATATAAT[C/G]AAGATCAAGAGGCTT | 51317 |
rs751035195 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45968790 | CAAAAATTAGCCGGG[C/T]GTGGTGGCACATGCA | 51317 |
rs751040961 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46058344 | CATTGTTGGTAAAAC[G/T]AAACCTGATTAAGAC | 51317 |
rs751041548 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46118420 | AAAGTCTGATGTTAA[-/A]AAAAAAAAAAAAAAA | 51317 |
rs751044098 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45991721 | TCAGTTATTTACCCA[A/G]TCTTGGTCTCAGCTT | 51317 |
rs751045065 | snp | C/T | 4.95054e-05 | 0.00497496 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45935703 | TGTTTTAAATCTGAA[C/T]TCCATTTAAGTAACT | 51317 |
rs751058019 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45931832 | ACAAATCTGACACAA[C/T]TTACTTCTGACAAGG | 51317 |
rs751065490 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:45973078 | GTGAGACTTCGTCTC[-/A]AAAAAAAAATAAATA | 51317 |
rs751080422 | snp | G/T | 1.66178e-05 | 0.00288247 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45953595 | GGCTCTCTGTTTGTT[G/T]CTCATCTGTTTCTGT | 51317 |
rs751081973 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46057213 | CTTGTTTATTTTCCA[C/T]CTTGGAACTACATAA | 51317 |
rs751084334 | snp | A/G | 6.75394e-05 | 0.00581078 | intron-variant | PHF21A | GRCh38.p7 | 11:45935766 | AAAAAAAAAAAAAAG[A/G]AACGGTTTTTGACAA | 51317 |
rs751098755 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46022621 | CACATGCCACCATGC[C/T]AGTGTAGTTTAATAT | 51317 |
rs751102550 | snp | A/G | 1.65192e-05 | 0.00287391 | intron-variant | PHF21A | GRCh38.p7 | 11:45950192 | AAGGCAGTGCCAAGA[A/G]TATCTTCTCTTACCT | 51317 |
rs751116160 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45937626 | GCTGGGATTACAGGC[A/G]CCTGCCACCATGCCC | 51317 |
rs751119670 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46110425 | TGTCAAAGGTCTCTA[C/T]ACTGAATCTACATGG | 51317 |
rs751132403 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46005197 | TCCAAAACTTTTTGA[A/G]CACTGACGTGATGCC | 51317 |
rs751160306 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46087979 | CTAGGCTGGTCTTGA[A/G]CTCCTGGGCTAAAGT | 51317 |
rs751189182 | snp | A/C | 3.31257e-05 | 0.00406962 | intron-variant | PHF21A | GRCh38.p7 | 11:46076706 | CTCGAGCAGACATAT[A/C]TTTAGAACACAACGT | 51317 |
rs751203422 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45967966 | TCTGGTTACAATCCA[A/C]TAAACTGCTTTCACA | 51317 |
rs751234982 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46020752 | TGTCCTATAAAGCCA[C/T]GATAGTTATGGTTGA | 51317 |
rs751250282 | snp | C/G | | | upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46122380 | CCTCGCCACCCCGCC[C/G]CCTTTCCAAATAACT | 51317 |
rs751260183 | in-del | -/CAC | | | intron-variant | PHF21A | GRCh38.p7 | 11:46040926 | ACACACACACACACA[-/CAC]ACACACGCACGCACA | 51317 |
rs751276855 | snp | C/T | 3.49247e-05 | 0.00417865 | intron-variant | PHF21A | GRCh38.p7 | 11:45953487 | TGAGAATAAACCATA[C/T]ACCATAGACTGAGAC | 51317 |
rs751326991 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46034642 | TCCAGCTCATGACAG[C/G]TCTCCCAGTGGCTAT | 51317 |
rs751330355 | snp | G/T | 1.80442e-05 | 0.00300363 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45933962 | GCTTCTCCTAGAGGG[G/T]CTCTGTTATTTAGTC | 51317 |
rs751353654 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45998212 | TGTTATTAGCACACA[A/G]ATTTAAAGCAGTTTA | 51317 |
rs751359959 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46033272 | TTGTTGTTAGTATTA[C/T]TGTTGTTGTTGAGGC | 51317 |
rs751365166 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45943068 | TATGCAGACGTGATC[A/T]CTTTTCTCCATCTCT | 51317 |
rs751369872 | in-del | -/ATT | | | intron-variant | PHF21A | GRCh38.p7 | 11:45974424 | AAACGACAAATTATT[-/ATT]ATTATTATTATTATT | 51317 |
rs751383046 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45981081 | GGTTCACAACTATAC[A/T]CTGCACTTATAACTA | 51317 |
rs751390892 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46059465 | CAGGGTTCCACTGTC[A/G]CCCAGATGGGAGTGC | 51317 |
rs751448466 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46048010 | AATTCATATATCACA[C/T]AATTCATCCATCTGA | 51317 |
rs751449650 | snp | A/G | 2.27803e-05 | 0.00337486 | intron-variant | PHF21A | GRCh38.p7 | 11:45965625 | TATAGGGGAAAGAGA[A/G]AATAATTATTGTATT | 51317 |
rs751455267 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45959806 | CATGTAACTGGTAAG[A/G]GTCTAGTATCCAGAT | 51317 |
rs751476620 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46011311 | CTGCCCAACATGGTA[A/C]AACCCTGTCTCTACT | 51317 |
rs751524506 | snp | C/G | 1.80052e-05 | 0.00300038 | intron-variant | PHF21A | GRCh38.p7 | 11:45945814 | AAGCTCTCAGAAAGA[C/G]AGTGTGCTTTTCCCA | 51317 |
rs751530062 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46062951 | GGACTGGATTGACAG[A/T]AGGATGAGCGAGACG | 51317 |
rs751530482 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45931019 | TGAGTGCAGAATGTA[A/G]GTTTGGGGGCTGGGT | 51317 |
rs751536501 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46046573 | AGAAGCCATTCTAAG[A/G]CAATCTCACAGAGGC | 51317 |
rs751551633 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46057060 | CACACAAAAAATATT[A/T]TTGACATTAATCTGT | 51317 |
rs751580003 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45934417 | AGGGCGGGTGGAGTG[A/G]GTAGGCTGGGGGGTC | 51317 |
rs751598787 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46038464 | ATTTATTGAGCACCT[C/G]CATGTGCTACATACT | 51317 |
rs751598879 | in-del | -/AA | | | intron-variant | PHF21A | GRCh38.p7 | 11:45987660 | GCAAGACCCCGTCTC[-/AA]AAAAAAAAAAAAAAA | 51317 |
rs751621286 | snp | G/T | 9.89674e-05 | 0.00703377 | intron-variant | PHF21A | GRCh38.p7 | 11:46084140 | TACTTAACAACAGTG[G/T]GGGAGAAGCCAATAA | 51317 |
rs751635128 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46073541 | AAAATATACATAAGA[A/G]TATACAGAAAAAATA | 51317 |
rs751642081 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45986840 | AATTATATTTCAATC[A/G]CTTGATTTTTAACAT | 51317 |
rs751722849 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46090436 | AGGATAAGAGTCGTA[C/T]AAAAAAGGAATGGGT | 51317 |
rs751748943 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45999937 | GTGCTAAGAGAAAGT[C/T]GCAATATTCTGCAAG | 51317 |
rs751755568 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46016779 | AGCCCTCAGAAATGT[C/T]TGGTAAACTGAACTG | 51317 |
rs751774307 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46050987 | AATATAGCAGTCTCC[A/G]AGTTCTCTGTGCCAT | 51317 |
rs751783486 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46105083 | CCTCATAACCACTTC[A/G]TTTTATTCAAATTTT | 51317 |
rs751790364 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45946835 | TATGAGGGTGGAGAC[C/T]GGCAAAGCAAGGAGG | 51317 |
rs751798628 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46088810 | GACTGTAGGCTTTTC[C/T]GTTCTCAAATTCTCT | 51317 |
rs751808135 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46065673 | CTCAGAGAAATTCAA[A/T]GGACACAAAGCCTGT | 51317 |
rs751839230 | snp | C/T | 1.64841e-05 | 0.00287085 | synonymous-codon, missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934160 | AATCAGCTGTTTTAC[C/T]TTCTCCAGGGAGCTG | 51317 |
rs751840265 | in-del | -/AA | | | intron-variant | PHF21A | GRCh38.p7 | 11:45967368 | GTGAGACCCTGTCTT[-/AA]AAAAAAAAAAAAAAA | 51317 |
rs751855492 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46016689 | TGTTTTTCTCCTCTA[C/T]TATACTGCCAGCACC | 51317 |
rs751860563 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46050016 | GTCACCACATGTTCA[A/G]TTTGCTGTAGGGCTC | 51317 |
rs751930327 | snp | A/G | 1.64749e-05 | 0.00287005 | missense, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45971223 | GCACATCAGTGCTGA[A/G]CACAGCCTTCTGACT | 51317 |
rs751939079 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46014335 | CATGTTGCTGCAAAG[A/G]ATATTATGTTGTTCT | 51317 |
rs751948120 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46064588 | ACCATAAAAAGATAC[C/T]AGTTAAAGAGTAAAC | 51317 |
rs751974946 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46069517 | AGAGGCTGGAGATAG[C/T]CATATATCAGGTAAC | 51317 |
rs751981172 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46034211 | GAGTTGCCTTAATAT[A/T]AGTGCCCCCACCCCC | 51317 |
rs751988938 | in-del | -/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46105477 | TTCTCCACACTCAGA[-/C]CCACACTAACCAGGA | 51317 |
rs752001261 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46067856 | AGTACCACAATGAGC[C/G]CCAAATAAAGTAGGC | 51317 |
rs752016931 | in-del | -/AAAA | 0.38637 | 0.209531 | intron-variant | PHF21A | GRCh38.p7 | 11:45935742 | TCTTCTTCTTTTGCT[-/AAAA]AAAAAAAAAAAAAAA | 51317 |
rs752027015 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46029987 | TTGATTTGATAAATA[C/T]CCTCCTCACTCAAAT | 51317 |
rs752035023 | snp | C/G | 4.9423e-05 | 0.00497082 | intron-variant | PHF21A | GRCh38.p7 | 11:45948848 | ACACACAAAGCAAAA[C/G]CAACAGCAGCAAGGG | 51317 |
rs752069857 | in-del | -/A | 1.80686e-05 | 0.00300566 | intron-variant | PHF21A | GRCh38.p7 | 11:45971412 | CACTAAATCTAAACT[-/A]AATAATAAACTAAAT | 51317 |
rs752078877 | snp | C/T | 3.30246e-05 | 0.0040634 | intron-variant | PHF21A | GRCh38.p7 | 11:46079205 | GCCATCAGTCTTACA[C/T]ATTAACTCCCTATGG | 51317 |
rs752087890 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45993070 | TCCAACCAGAACACT[A/G]AAACTAACATCTTTT | 51317 |
rs752111715 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46042710 | TAGGTCACGAGGGCC[C/T]TCCTTCACAAATGAG | 51317 |
rs752112861 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46028930 | ATGTGTATTACTATG[A/C]CCCAAAGGACTATAT | 51317 |
rs752135584 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45994137 | TGCTAACCTTACAGC[C/T]TCAAGCCAAAAACTT | 51317 |
rs752190000 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45976603 | TCCCAACACTGTGGG[A/T]GACCGAGATGGGTGG | 51317 |
rs752198646 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46080273 | AAGTTATCCTTCCAC[C/T]TCAGCCTCCCGAGTG | 51317 |
rs752198995 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46042953 | GGTATTTTGTTATAG[C/T]AGCCTGAATGAACTA | 51317 |
rs752213589 | snp | C/T | 1.70609e-05 | 0.00292065 | downstream-variant-500B, stop-gained, synonymous-codon, utr-variant-3-prime | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45928819 | CTCCCAGCCCTGCAG[C/T]AGCCCCAGAGCCCTG | 51317 |
rs752213799 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46044034 | CTGTAAATTTGTTTT[C/T]ACCTTCATAGAGTAA | 51317 |
rs752215628 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46001408 | GTACTTAGCCAATGC[A/G]CCTGTAGATTCTAAT | 51317 |
rs752225934 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46008075 | TGAAAATTAACACGA[A/C]GTGAAGTTCAGAAAG | 51317 |
rs752232127 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46112918 | TATATTATTTTGTGT[A/G]TAAACCTTATAGTAG | 51317 |
rs752233590 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45966305 | CTCATCAATTTCTTC[C/T]TCCAATCTTCTCTTC | 51317 |
rs752263783 | in-del | -/AT | | | intron-variant | PHF21A | GRCh38.p7 | 11:46032842 | CCATTAATGATTTTA[-/AT]ATGTTTAATGATTCA | 51317 |
rs752277085 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46114574 | GTCAATACAACATAC[C/T]GTCCATAAGGCCAGA | 51317 |
rs752278112 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45993316 | GTAATCACATATTTA[C/T]ACAGCACTTTACGAT | 51317 |
rs752305378 | in-del | -/TAAACTA | | | intron-variant | PHF21A | GRCh38.p7 | 11:46080531 | ATTATATTAATATAC[-/TAAACTA]TAAACAATAGGTTCC | 51317 |
rs752332956 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46058444 | CAGGAACTTAGTCTT[A/G]TAGGACTGATATATT | 51317 |
rs752378703 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46095055 | GGCTTTAATTGGTTT[C/G]ACAATGAGGTTCACA | 51317 |
rs752420937 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46072080 | TTCCCTGACTTCCTG[A/G]AACTAACAATCTAAT | 51317 |
rs752421334 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46024086 | ATTGGTTATGAAAGC[A/C]AGGAAAGGGCAAGGT | 51317 |
rs752422069 | snp | A/G | 3.36729e-05 | 0.00410308 | intron-variant | PHF21A | GRCh38.p7 | 11:46076852 | ATATCTGTGAGAAAG[A/G]TATTTCATTTGTTAA | 51317 |
rs752422990 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46057520 | TATAAAGGGAAAAAC[C/T]GTACTTTCTGTTCTC | 51317 |
rs752426464 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46031556 | AGTAGTTCATGCAGC[C/T]GGTACGAATTCATTC | 51317 |
rs752463587 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46110715 | CTTATAAAGTAGAAG[A/C]ATATCAGACCAGATT | 51317 |
rs752471083 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45933640 | AAACAGAAACAAACC[C/T]ATCGTGGCTGTGGAG | 51317 |
rs752512926 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46070716 | CTATCTCTCTAAAAA[C/G]GAGTAAAAAGAAATA | 51317 |
rs752524844 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45984673 | GACTGCCCCCACCCA[A/G]TCAACCCACCAGTTT | 51317 |
rs752540362 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45944581 | ACCCTGGCCAGCTTG[C/T]TCTGCCCCCGCTATC | 51317 |
rs752547598 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46020331 | CTGAAGTGGCTGCTA[C/G]TATCCTGCAGCAAAC | 51317 |
rs752548665 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46086777 | TAACATAAAACCATA[C/G]TTCAATTCAATTCAC | 51317 |
rs752557278 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46088360 | TTGCAATCTTCCAAA[C/T]GGTACATGTCAAACC | 51317 |
rs752583357 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46049701 | AGCCGCTGTCCTACT[C/T]AGGGGGTCCCCTCCA | 51317 |
rs752601368 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46035732 | TGGGGAGGAGAACAG[C/T]GTCTCAGAAGGGAGA | 51317 |
rs752614428 | in-del | -/AGCCT | | | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45932147 | AGGGCTGATGCAGCC[-/AGCCT]AGCCTGTACTCCCGC | 51317 |
rs752635361 | snp | A/T | | | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934055 | GGTGGCGGCATTGGC[A/T]GGGGGGGTGCAGTCC | 51317 |
rs752662117 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45998504 | CATGCAAAATAACTC[C/T]ACCATTTCTTTTTCT | 51317 |
rs752695673 | snp | C/T | 3.43383e-05 | 0.00414343 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45965509 | TGGGGGTGAACTTGG[C/T]CAGCATGACGGGCCT | 51317 |
rs752721147 | snp | A/G | 1.65625e-05 | 0.00287766 | intron-variant | PHF21A | GRCh38.p7 | 11:46076711 | GCAGACATATCTTTA[A/G]AACACAACGTTAAAA | 51317 |
rs752745939 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46014872 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 51317 |
rs752788110 | in-del | -/CTCTCT/T | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:46121165 | TCCTCCTCTCCTCTC[-/CTCTCT/T]CTCTCTCTCTCACTC | 51317 |
rs752817042 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45973130 | AATTAAATGTAATTA[A/G]TTAAAACAAAAACAA | 51317 |
rs752834981 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46073930 | CCTTCCAACCAAGAA[C/T]TCAGTGAAATTCACT | 51317 |
rs752837908 | snp | C/T | 1.64784e-05 | 0.00287035 | missense, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45938256 | GGAACATGTGTCGCA[C/T]ATCAGTAACTGGCCA | 51317 |
rs752845361 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46075456 | AGCGCTAACAGAATT[C/G]TAAAGCTAGAACACT | 51317 |
rs752890173 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45987376 | ACCATAAAAAAGCAC[C/T]TGAGGCCAGGCGTGG | 51317 |
rs752901378 | snp | A/G | | | downstream-variant-500B | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45929146 | CTCTGGGGCTAGGGC[A/G]TCAGTGCACAAGGGA | 51317 |
rs752903995 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46039771 | CAGGATCTCAGTCAA[A/C]ACTGCACAATCTGCA | 51317 |
rs752904893 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45988719 | CATGGCAAAAATCCC[A/G]TCTCTACAGAAAATA | 51317 |
rs752906799 | snp | A/G | 1.64863e-05 | 0.00287104 | intron-variant | PHF21A | GRCh38.p7 | 11:46084160 | GAAGCCAATAATACA[A/G]CTTACCTGGTGAACC | 51317 |
rs752935762 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46091983 | ACATGCAGGCCTAGC[G/T]GTATTAGCAGAAACA | 51317 |
rs752969599 | snp | A/G | 1.64895e-05 | 0.00287132 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934177 | TCTCCAGGGAGCTGT[A/G]CATCTCCTTCTGCCG | 51317 |
rs752978752 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46106931 | TTCACAGAAAGAAAG[A/G]CTGTTTCTTTAAAAT | 51317 |
rs753047910 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45944496 | GTAATGGTCTCCCAT[C/T]TTACTGAGAACGAAA | 51317 |
rs753051511 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46067328 | GTATGTATGAGTTCA[A/G]TGGGGAGGCGGGCAT | 51317 |
rs753058630 | snp | C/G | | | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45965478 | TGGATGGAATTCTGG[C/G]ATGTGGGAAGGGTTG | 51317 |
rs753066631 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46105363 | CATGTGTGCCAGACG[C/T]CTTTACAGGCACACA | 51317 |
rs753075835 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46017989 | GGCGCGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 51317 |
rs753086590 | snp | C/T | 1.64743e-05 | 0.00287 | intron-variant | PHF21A | GRCh38.p7 | 11:45949370 | AATAAAACTGGAACA[C/T]GAGGGAAGGGCCAGA | 51317 |
rs753091988 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46001648 | CATTTTTAAAATTCC[A/G]TTAGTATCTTGCCAG | 51317 |
rs753096501 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45978259 | TGAGCCAAGACTGCG[C/T]CACTGCACTCCAGCC | 51317 |
rs753105422 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45946888 | TATCCCTTGCTTTTA[A/G]AGCTATTGAGAGGCA | 51317 |
rs753105898 | in-del | -/CACT | | | intron-variant | PHF21A | GRCh38.p7 | 11:46099976 | TTGATCCTTTCTCAC[-/CACT]GCTATCCTTAATGAA | 51317 |
rs753110002 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46064605 | GTTAAAGAGTAAACT[C/T]CTTTTTCCTGTCTGG | 51317 |
rs753149724 | in-del | -/AAATCTGAACTCCATTTAAGTAACTTCTGTTTCTCTTCTTCTTTTGC | 1.64901e-05 | 0.00287137 | splice-acceptor-variant | PHF21A | GRCh38.p7 | 11:45935694 | TCTCGTTCTTGTTTT[lengthTooLong]TAAAAAAAAAAAAAA | 51317 |
rs753159036 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46098009 | TCCCCCAAAAGATTC[-/T]TAATAGGGAGCCAGG | 51317 |
rs753169487 | in-del | -/AAGA | | | intron-variant | PHF21A | GRCh38.p7 | 11:45957722 | CTAACTTTACACCTT[-/AAGA]AACAGAAAAAGAACT | 51317 |
rs753183759 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46016766 | CCTGGAGCTTGGCAG[C/T]CCTCAGAAATGTTTG | 51317 |
rs753197489 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46096720 | GAACTCTTCCCCTTA[C/G]GTGATCTCACACAGT | 51317 |
rs753208477 | in-del | -/AC | | | intron-variant | PHF21A | GRCh38.p7 | 11:46015991 | ACACATAAACTGATA[-/AC]ACAGTCATTTATTAT | 51317 |
rs753228175 | in-del | -/GAG | | | intron-variant | PHF21A | GRCh38.p7 | 11:46103962 | AAACTCCTCAAATCT[-/GAG]GAGATCATTGTACCT | 51317 |
rs753240794 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45978072 | TTTGGGAGGCCGAGG[C/T]GGGCAGACCACGAGG | 51317 |
rs753244051 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46065794 | AGCGGGTGTATAAGG[G/T]TGAAGGGATCACAGT | 51317 |
rs753247469 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45937762 | CTGAGATTACAGGCC[C/T]GAGTCACCACGCCTG | 51317 |
rs753258099 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46016988 | TTTTTTTTTTTTAAT[C/T]GAGATGGAGTCTCAC | 51317 |
rs753274470 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45979347 | AAATGCTTCTTTCTA[G/T]CTGGTCCCAAGAGCA | 51317 |
rs753309318 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46081826 | ACTCATTCATTTATA[G/T]ATTGTCCGTGGCTGT | 51317 |
rs753318547 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46032867 | TGATTCATACAAGAG[C/T]ATAAGTACATGTGTG | 51317 |
rs753330592 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46067877 | TAAAGTAGGCACAAG[C/T]ACCAAGTACCATGAG | 51317 |
rs753337160 | snp | G/T | 1.64743e-05 | 0.00287 | intron-variant | PHF21A | GRCh38.p7 | 11:45979747 | GCCTGCAATGTTCCA[G/T]CCACACATTTACCTG | 51317 |
rs753350908 | snp | A/G | 0.000293315 | 0.0121067 | downstream-variant-500B, utr-variant-3-prime, synonymous-codon | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45928861 | GGCTGGGCCGGCGCT[A/G]CCCCTCATCTTAGCA | 51317 |
rs753366255 | in-del | -/GT | | | intron-variant | PHF21A | GRCh38.p7 | 11:46064324 | CGAGCAGGAGAAAAG[-/GT]GACAACTGAACAGAT | 51317 |
rs753366425 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45996274 | ATCCTATTAAAAACA[C/T]AGGATCTAGTACTCA | 51317 |
rs753406865 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46031780 | ATTTTTTTCCAGAGA[A/C]GTTACTAACACTATA | 51317 |
rs753446335 | in-del | -/AG | 2.61141e-05 | 0.00361336 | intron-variant | PHF21A | GRCh38.p7 | 11:45969932 | GAAGATAAATAAACC[-/AG]AGAGAACAATTACTC | 51317 |
rs753454505 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46017577 | AGGATTTGCCCTTAA[-/G]GGGGGAAAAAAAAAA | 51317 |
rs753466737 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45978230 | GTTTGAACCCAAGAC[A/G]GTGGAGGTTGCAGTG | 51317 |
rs753502294 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45939202 | ATTAACATTATAGGC[A/G]ATACCTAAGAGTTTT | 51317 |
rs753508553 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46080628 | CAGTCCACTCCTTAA[C/T]GTCAAGTAGTCAGCC | 51317 |
rs753517625 | snp | C/T | | | intron-variant, downstream-variant-500B | PHF21A | GRCh38.p7 | 11:45934850 | TGCTGGCTTCTATTT[C/T]AGGCAGGGAAAGAGA | 51317 |
rs753542180 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46017313 | TTTGCTATCTTCTCA[C/T]AGTTCTAGCAAAGGA | 51317 |
rs753543756 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46114236 | AGCTATCAGTAACAC[A/G]TCCAAACACAAGCTG | 51317 |
rs753545133 | snp | C/G | 3.45072e-05 | 0.0041536 | downstream-variant-500B, missense, utr-variant-3-prime | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45928827 | CCTGCAGCAGCCCCA[C/G]AGCCCTGCCCGAGGC | 51317 |
rs753558110 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46060751 | AGTTTGCAAACATTT[C/T]CTCCCATTCTGTAGG | 51317 |
rs753565452 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46009859 | CATCTGGTATAACTC[C/T]TTCATCACCTTGCAT | 51317 |
rs753576258 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45955390 | GACATTTTAAAGTCC[C/T]GGATGCCCAGAAATC | 51317 |
rs753582517 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46097175 | TTCTACCCTAGCCCC[A/G]CTAAGGTATATTCTC | 51317 |
rs753612232 | in-del | -/AG | | | intron-variant | PHF21A | GRCh38.p7 | 11:46073869 | ACTTTGAAATCTGCC[-/AG]AGTTTCTTTCAGAAA | 51317 |
rs753622476 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46058789 | TCTCTTTACAAAATC[C/T]GGAACAAGAACAAGC | 51317 |
rs753631848 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46112748 | TTACGGAACAACTAT[C/T]CCCATTTTAAAAAAA | 51317 |
rs753644110 | snp | C/G | 1.71481e-05 | 0.0029281 | intron-variant | PHF21A | GRCh38.p7 | 11:45938119 | GGCCGTGTCTTTGTC[C/G]TCCTCGGCCCCTCCC | 51317 |
rs753654604 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46008347 | CTGTGAAGCATATCC[A/G]GGACACTATGGACCA | 51317 |
rs753660283 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45969455 | GCTGTTGTTTCCTTC[C/T]CTACTCTTTTTGGCA | 51317 |
rs753664675 | snp | C/T | 3.30726e-05 | 0.00406635 | intron-variant | PHF21A | GRCh38.p7 | 11:45936447 | TGCCAGTATTTTTTT[C/T]AAACAAGGGGAAGCT | 51317 |
rs753692133 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46083695 | AGCTTTTTGTAAAAT[A/G]TAAGAATTGTGAAAT | 51317 |
rs753706815 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46081500 | CACTGGAATTTAAAA[A/C]TTCACTGATAACCAC | 51317 |
rs753712133 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46073223 | GTCCCAGCTACTTGG[G/T]AGGCTGAAGTGGGAG | 51317 |
rs753721014 | snp | G/T | 1.69726e-05 | 0.00291308 | intron-variant | PHF21A | GRCh38.p7 | 11:46076861 | AGAAAGATATTTCAT[G/T]TGTTAACAGAATAGT | 51317 |
rs753757359 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46080167 | TTTATCTAACTACTA[-/G]TTTTTTTTTGAGACA | 51317 |
rs753758211 | in-del | AATATTTTTCCCCCTCATGTTATTTA/CTATATTGCTCAG | | | intron-variant | PHF21A | GRCh38.p7 | 11:45981420 | AAAAAAAAAAAAAAA[lengthTooLong]TAAATGTCCTTGTTC | 51317 |
rs753776131 | in-del | -/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45984083 | TTATCCTGAAGCTTT[-/C]GAGAAAGGGCTAAAT | 51317 |
rs753782589 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46000386 | AGATATGATAGTACT[C/T]ATAGCACTTCTGAAT | 51317 |
rs753813818 | in-del | -/AAAT | | | intron-variant | PHF21A | GRCh38.p7 | 11:46111479 | GACTCCGTCTCAAAT[-/AAAT]AAATAAATAAATAAA | 51317 |
rs753842741 | snp | A/G | 1.67449e-05 | 0.00289347 | synonymous-codon, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45945864 | GGTGGGGCTGGGCAG[A/G]GACACAGGCTGAACA | 51317 |
rs753842887 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46023103 | TCAGACCTTGAGTGA[C/T]ATGTGGACAATCTGG | 51317 |
rs753892419 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45997626 | TAAATGCTTGTTTTG[C/T]AGCCTTAAAAGTGGC | 51317 |
rs753922676 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46048273 | TAAGGCCTTTTGTCA[C/T]TGGCTTCTTTTACTT | 51317 |
rs753974876 | snp | C/T | 1.78912e-05 | 0.00299086 | synonymous-codon, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45933983 | TTATTTAGTCTCTTC[C/T]CCCTGGTTACAGTTC | 51317 |
rs753991831 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46090423 | AAAGGAAGAACTAAG[A/G]ATAAGAGTCGTACAA | 51317 |
rs754042061 | in-del | -/ATAA | | | intron-variant | PHF21A | GRCh38.p7 | 11:46108584 | TATATATATATATAT[-/ATAA]ATAAAATACATATGT | 51317 |
rs754043511 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45989119 | AATTACTGATTAACT[G/T]CATGGAATTGGCTCT | 51317 |
rs754050644 | in-del | -/AG | | | intron-variant | PHF21A | GRCh38.p7 | 11:46117329 | TCACCTAACACTAAC[-/AG]AGTTTCAAAGGACCA | 51317 |
rs754056660 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45974648 | TTAGTAGAGACGTGA[G/T]CTCGCTATGTTGCCC | 51317 |
rs754067061 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46116301 | CCTAATACTAACACA[C/T]ACAGATATACATCTT | 51317 |
rs754092724 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46075719 | TGGAAGATGATTCTA[C/T]TCTGAAACATTAATG | 51317 |
rs754100665 | in-del | -/AG | | | intron-variant | PHF21A | GRCh38.p7 | 11:46035815 | TTAGAGTTTGAAGAA[-/AG]AGAGAGAGAGAAAAG | 51317 |
rs754107724 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46106922 | CTTCAGCCTTTCACA[A/G]AAAGAAAGGCTGTTT | 51317 |
rs754136407 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46104096 | CATCAGGCACCAAAT[C/G]AGAGGAAATTTCACA | 51317 |
rs754138626 | in-del | -/GAAAAA | | | intron-variant, cds-indel, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46119744 | CGAACGTGGTCAGGG[-/GAAAAA]AAAAAAAAAGAAATC | 51317 |
rs754141020 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46093321 | CCAATAGTGTCTCAT[C/T]GCCTCAGGGAATATT | 51317 |
rs754182092 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45977640 | ATCCTCTAAACATTC[C/T]TTCAGAACTAATACA | 51317 |
rs754200680 | snp | C/T | 1.88677e-05 | 0.0030714 | intron-variant | PHF21A | GRCh38.p7 | 11:45935554 | GAAACAGCCTGGGGC[C/T]CACACGTACTGTTAC | 51317 |
rs754208279 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45949971 | CCTAAATGAACAGAA[A/G]TCACCTGAATTTAGG | 51317 |
rs754235811 | snp | A/T | 1.64806e-05 | 0.00287054 | missense, utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45979864 | GTTGCTGCTGTGCTG[A/T]TTGTAGTTTGTTTTC | 51317 |
rs754271839 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45975767 | AAAGCAAACTGTTCC[C/G]ATTCCCTCTCCCAAA | 51317 |
rs754277810 | snp | A/G | 1.64735e-05 | 0.00286993 | intron-variant | PHF21A | GRCh38.p7 | 11:45949378 | TGGAACATGAGGGAA[A/G]GGCCAGATGCTGGCC | 51317 |
rs754306121 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46054817 | CTGAATGAATTAAAT[A/G]TTGAAAGATTACCTT | 51317 |
rs754316971 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46107045 | TCTGCAGGAAGAATG[A/G]CCTATCTTGAGCACT | 51317 |
rs754325904 | snp | C/T | 0.000185477 | 0.0096283 | intron-variant, downstream-variant-500B | PHF21A | GRCh38.p7 | 11:45935083 | TGCAAATACAACCCT[C/T]TTTCCCACTTGGACA | 51317 |
rs754336032 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46039454 | GGGGAAGCCTGAGAA[C/T]AGTCAGGTAAGTACA | 51317 |
rs754367741 | snp | C/T | 1.66269e-05 | 0.00288326 | intron-variant | PHF21A | GRCh38.p7 | 11:45950156 | CATCATTTTCAGGAA[C/T]AAAGCTGTGGGCCAG | 51317 |
rs754381433 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46068704 | TCCAGTCAGTAGATT[A/C]TAGTAGCCCAGTGTC | 51317 |
rs754393987 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46053214 | TCACATCTCTCATGG[A/G]TAGCAGAATAAAACA | 51317 |
rs754419864 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45937634 | TACAGGCGCCTGCCA[C/T]CATGCCCGGCTAATT | 51317 |
rs754433333 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45993085 | GAAACTAACATCTTT[G/T]ACATTTAACTGGTTC | 51317 |
rs754500229 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45997640 | GCAGCCTTAAAAGTG[G/T]CAGACAAATTAAAAT | 51317 |
rs754509507 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46077435 | TGAGATACACAGAGC[A/T]TGATTGCCTTTTACT | 51317 |
rs754525806 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46006487 | ACCTCCACAAATCAC[A/G]CTATATAAATAACAA | 51317 |
rs754611272 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46057434 | ACAGATGCCCAGAGC[A/T]TTAGGGCTTAATTTT | 51317 |
rs754615406 | snp | C/T | 1.7501e-05 | 0.00295807 | intron-variant | PHF21A | GRCh38.p7 | 11:45935575 | GTACTGTTACGTATA[C/T]TGGAAAGGCCTAGGT | 51317 |
rs754615899 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46005305 | AAATGATGTAAAATA[C/T]TGTATAAAATTTATA | 51317 |
rs754621014 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46110453 | TGGCTGCCCAGTTTT[A/G]CTCTCCTTATTTCCT | 51317 |
rs754622691 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46093968 | GGACAAAATTAAAAT[C/T]AAGAACTTCTGCTCA | 51317 |
rs754661538 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45993921 | AAACTGCTCTAAGTA[C/T]TTGGAAAGGCTGGGA | 51317 |
rs754665435 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46020988 | TTTCAATGTATGATG[G/T]GTTTATTGGACCATA | 51317 |
rs754708897 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46108890 | CTATTAGACCCCACC[C/G]CATGCTACGCACTAT | 51317 |
rs754720020 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46052168 | GCTCTATGCTGGTAC[C/T]TCCAGGAAAAAACAA | 51317 |
rs754727403 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46064531 | GGGAAACATATCTTC[C/T]GAAAACATAATTTTG | 51317 |
rs754758566 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46069100 | CAGTCACACTACATA[C/T]ATACAACCTCTCGAT | 51317 |
rs754760188 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46017549 | AAGAGCTCCATATTT[A/G]TAAGTTACAGTTCAG | 51317 |
rs754829369 | snp | A/C | 0.000148604 | 0.00861859 | intron-variant | PHF21A | GRCh38.p7 | 11:45950196 | CAGTGCCAAGAATAT[A/C]TTCTCTTACCTTCTA | 51317 |
rs754833209 | snp | C/T | 3.31082e-05 | 0.00406854 | intron-variant | PHF21A | GRCh38.p7 | 11:46076709 | GAGCAGACATATCTT[C/T]AGAACACAACGTTAA | 51317 |
rs754848115 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45981090 | CTATACTCTGCACTT[A/G]TAACTATATTGCTGG | 51317 |
rs754850902 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:45984152 | TGAGAGTTAAAAGAG[-/A]GGGAAAAAATCAGGG | 51317 |
rs754856822 | snp | A/G | 2.48407e-05 | 0.00352416 | downstream-variant-500B, utr-variant-3-prime, missense | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45928893 | TGGGCAGACACCAGG[A/G]CAACCTGCCCTCCGC | 51317 |
rs754873508 | snp | A/G | 1.70069e-05 | 0.00291602 | missense, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45945850 | CTTACGTCTGTGGAG[A/G]TGGGGCTGGGCAGGG | 51317 |
rs754885588 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46048928 | TTCAAGTGGCTGTAA[C/T]ATTTTACATTCCCAC | 51317 |
rs754888300 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45963148 | CTGGGGGCCGGGTGC[C/G]GTGGCTCACACCTGT | 51317 |
rs754890625 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45931181 | TCAATTCCTAGCCCC[G/T]TCCTCCGACCCAAGA | 51317 |
rs754911690 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46033286 | ATTGTTGTTGTTGAG[A/G]CACAGTCTTACTCTG | 51317 |
rs754933765 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46082510 | TAAAATATTATTGAC[A/G]TATAAATAAATGTTT | 51317 |
rs754936395 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46048181 | AATTCCCCCAGCCCT[A/G]GGCAACCATTAATTG | 51317 |
rs754937092 | in-del | -/TTTTTTTTTTTT | | | intron-variant | PHF21A | GRCh38.p7 | 11:45981950 | TTTTCTTTTTTTTTT[-/TTTTTTTTTTTT]TTTTTTTTTTTTTTT | 51317 |
rs754944318 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46008788 | ATAAATGTAAATTCA[A/T]CTGCAAAATGCTATG | 51317 |
rs754945730 | snp | G/T | 3.60568e-05 | 0.00424583 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45933964 | TTCTCCTAGAGGGGC[G/T]CTGTTATTTAGTCTC | 51317 |
rs754965971 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46099872 | TAGCTCCACAACACA[A/G]ATAAAAAAGAACCCT | 51317 |
rs754974481 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46081689 | AGTTAGGTTACTTTC[C/T]GCCAGAATGCGGCAA | 51317 |
rs755013485 | in-del | -/ACA | 1.65551e-05 | 0.00287702 | intron-variant | PHF21A | GRCh38.p7 | 11:46076715 | ACATATCTTTAGAAC[-/ACA]ACGTTAAAAATATGC | 51317 |
rs755014892 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46025784 | AATTATTTGCAAGTC[A/G]TAGGCATAATATGGC | 51317 |
rs755022706 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46046594 | TCACAGAGGCCTTTC[C/T]AATCATTTTGTGCAT | 51317 |
rs755032513 | snp | G/T | 3.29511e-05 | 0.00405887 | missense, utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45979900 | GTGGCAATGGCTGTA[G/T]TTGGAACTTGTCCGG | 51317 |
rs755091215 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46090639 | CCACAGAAGCCTTTT[C/T]CCACCCCCACCCCAC | 51317 |
rs755097066 | snp | G/T | 1.68371e-05 | 0.00290143 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45969823 | TACTCACCTGTGGAA[G/T]AAAGTTTGGACGTGG | 51317 |
rs755168407 | snp | G/T | 4.93864e-05 | 0.00496898 | intron-variant | PHF21A | GRCh38.p7 | 11:46079092 | TTTATTTTAAATTAT[G/T]TTTAAATTTAACAAT | 51317 |
rs755203223 | in-del | -/AA | | | intron-variant | PHF21A | GRCh38.p7 | 11:45935743 | CTTCTTCTTTTGCTA[-/AA]AAAAAAAAAAAAAAA | 51317 |
rs755207356 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45989272 | TTTAAATCATTAGTA[C/T]TACAAATCTTATTAA | 51317 |
rs755214673 | snp | A/G | 1.64885e-05 | 0.00287123 | synonymous-codon, stop-gained, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934175 | CTTCTCCAGGGAGCT[A/G]TGCATCTCCTTCTGC | 51317 |
rs755221012 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45985101 | GATACTAAATTTTAC[A/G]CGTATGGAAAAACTA | 51317 |
rs755243761 | in-del | -/AG | | | intron-variant | PHF21A | GRCh38.p7 | 11:45951257 | AAGACATACTCCTGT[-/AG]AGTTATTTATACCAC | 51317 |
rs755248584 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46051123 | TCTCTCTGAGGTAAA[A/G]TACACCACATTTAAA | 51317 |
rs755258522 | snp | A/G | 2.26339e-05 | 0.00336399 | intron-variant | PHF21A | GRCh38.p7 | 11:45965278 | ATGCCTCAACGACAA[A/G]GCTACTGCCCAGAGC | 51317 |
rs755269945 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45946868 | AAATTCAAGTTAACT[A/G]TTCTTATCCCTTGCT | 51317 |
rs755290812 | snp | A/G | 1.64912e-05 | 0.00287147 | intron-variant | PHF21A | GRCh38.p7 | 11:46084143 | TTAACAACAGTGTGG[A/G]AGAAGCCAATAATAC | 51317 |
rs755338228 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46050077 | AGTCTTTCCCCAGCA[C/G]AGTTAGCGATTGCCA | 51317 |
rs755355368 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45961572 | TATGAAAAATATTTA[C/T]GGTAACGTGGCAATT | 51317 |
rs755359839 | in-del | -/CACACACG | | | intron-variant | PHF21A | GRCh38.p7 | 11:46040928 | ACACACACACACACA[-/CACACACG]CACGCACAATTAAGG | 51317 |
rs755361616 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45945052 | ACAGGCATAAGCCAC[C/T]ATGCCCGGCCCCATT | 51317 |
rs755384870 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46065679 | GAAATTCAATGGACA[C/G]AAAGCCTGTCAGTGA | 51317 |
rs755410646 | snp | G/T | 0.00297611 | 0.0384603 | missense, utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934063 | CATTGGCAGGGGGGG[G/T]GCAGTCCGGGCCATT | 51317 |
rs755420063 | snp | G/T | | | upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46122604 | GGAATCGGCCACGTA[G/T]AATCCGGCGGTTTGT | 51317 |
rs755441106 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45976528 | CCAGAATCTACCACA[C/T]AGATTGGTAGTACCA | 51317 |
rs755474903 | snp | C/T | 3.25061e-05 | 0.00403137 | intron-variant | PHF21A | GRCh38.p7 | 11:45969948 | GAGAGAACAATTACT[C/T]TTCAATATCAAAGCT | 51317 |
rs755494283 | snp | A/C | 1.64743e-05 | 0.00287 | missense, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45971233 | GCTGAGCACAGCCTT[A/C]TGACTGTTGATGGCG | 51317 |
rs755499268 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45975775 | CTGTTCCCATTCCCT[A/C]TCCCAAAAAGAATTC | 51317 |
rs755511499 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46117849 | CGCAATCGCACATCT[A/G]CTTTGTACAGTCAAA | 51317 |
rs755515889 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46013358 | ACTTAGTAGCTATCT[C/T]GGTTATCAGATCAAC | 51317 |
rs755516849 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46009550 | CAAGCACAGTTCTAA[A/G]CACGCTATGTATTAC | 51317 |
rs755518003 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46029991 | TTTGATAAATATCCT[C/T]CTCACTCAAATTTAT | 51317 |
rs755552087 | in-del | -/AC | | | intron-variant | PHF21A | GRCh38.p7 | 11:46097827 | ATCTCCCTAACTAGA[-/AC]ACACACACACACATA | 51317 |
rs755565783 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46056478 | GAGCTAATATCACAG[C/T]GAAGATTTTAAAACA | 51317 |
rs755567806 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46089700 | TAATAATGTTGTTTC[C/T]TATGAAATAAAAAAA | 51317 |
rs755580754 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45978092 | AGACCACGAGGTCAG[C/G]AGTTCGAGACCAGCC | 51317 |
rs755598735 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45939302 | GTTTCACAATATGAT[A/G]CAAACAATTCTCATC | 51317 |
rs755606438 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46029060 | TCTGACCATTACCTT[C/T]TCAAAACAAAATGTA | 51317 |
rs755607284 | in-del | -/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46001772 | CACAGGGCTGTCACT[-/C]GTACTAGAAAAACGT | 51317 |
rs755636877 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46064999 | TTATAACTTCATGGT[A/C]TTTCAGCATGCATAT | 51317 |
rs755644594 | snp | C/T | 1.64735e-05 | 0.00286993 | missense, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45971256 | TGATGGCGGTCACCA[C/T]AGCAATGGTAGGTCT | 51317 |
rs755645837 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46028379 | TACAGGCAATTCTCA[C/T]TTTGCTGAACTGGCT | 51317 |
rs755673375 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46030252 | TTTTAGTTTCTATTC[C/T]GATTTCTTTAAAAGG | 51317 |
rs755689332 | in-del | -/TGAACCCACAT | | | intron-variant | PHF21A | GRCh38.p7 | 11:46063831 | TACTGTTTCATCTGA[-/TGAACCCACAT]TGAACCCACATCATA | 51317 |
rs755699822 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45994313 | TGATTCACTAACAGA[C/T]TTATCTTACTGCCAT | 51317 |
rs755715062 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45993372 | AATAAGACTCTCAGA[A/T]CTGTGCAGGGCTAAT | 51317 |
rs755768538 | in-del | -/AAA | | | intron-variant | PHF21A | GRCh38.p7 | 11:45935742 | TCTTCTTCTTTTGCT[-/AAA]AAAAAAAAAAAAAAA | 51317 |
rs755808954 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46006784 | CTACAATAAAAATGG[C/T]ACAAAAATATTTTAA | 51317 |
rs755822359 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46042239 | TGACAAAACATATTC[C/T]TCAATAAGGCATATT | 51317 |
rs755829269 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45969383 | CCTTTAAGCATGATT[C/T]TCAAAACCATCACTT | 51317 |
rs755830357 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46058604 | TAATAAAATGACTGA[A/C]CCTAAACATGGACAG | 51317 |
rs755846719 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45953777 | GTATTATAGATTTCA[C/T]TGGGGGAGGGGAAAC | 51317 |
rs755857049 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46095249 | CAGCAAAAAGCAAGA[C/T]CTATACACACGTTTG | 51317 |
rs755912918 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45933712 | TATATTATTTCACTT[A/G]GCATGGTGCTGGCAA | 51317 |
rs755937141 | in-del | -/CT | | | intron-variant | PHF21A | GRCh38.p7 | 11:46062701 | GTGGAGCAGCTAGAA[-/CT]CTCTCATACACTACT | 51317 |
rs755954176 | snp | A/G | 2.29613e-05 | 0.00338823 | intron-variant | PHF21A | GRCh38.p7 | 11:45953646 | AGAGAAAAATTAAAT[A/G]AAAATTCAGAATTCG | 51317 |
rs755967510 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45942989 | TAGGCCAAAAACTTT[-/G]GTTTTCTCCTTGACC | 51317 |
rs755970576 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46005354 | CAGAAGTGTTTCAGA[C/T]TTTGAGATTTTTCAG | 51317 |
rs755983333 | snp | A/G | 1.65471e-05 | 0.00287633 | intron-variant | PHF21A | GRCh38.p7 | 11:46076712 | CAGACATATCTTTAG[A/G]ACACAACGTTAAAAA | 51317 |
rs755989673 | snp | C/T | 1.69464e-05 | 0.00291083 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45935728 | GTAACTTCTGTTTCT[C/T]TTCTTCTTTTGCTAA | 51317 |
rs755996940 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46109014 | CTCAACCTAACCCAA[A/C]CAAAATCAACATGAA | 51317 |
rs756005968 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46023033 | TGAGATTATGGGCAT[A/G]AGCCACCGCGCCCGG | 51317 |
rs756015733 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45993560 | AAAAGCTGGAGCTCA[A/T]TTTTCTGAGCCAACT | 51317 |
rs756072384 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45997218 | GTATGAAACAGAGGG[A/G]TTTTTTTCCATGAAT | 51317 |
rs756076448 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45983200 | TGCATTCACAACTGC[C/T]CCTCCCCCAGGGCCT | 51317 |
rs756114307 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45957980 | GGATTATAGGAGAAT[A/G]TATTGAAAAACTGTA | 51317 |
rs756144454 | snp | C/T | 1.69026e-05 | 0.00290706 | intron-variant | PHF21A | GRCh38.p7 | 11:46076855 | TCTGTGAGAAAGATA[C/T]TTCATTTGTTAACAG | 51317 |
rs756187278 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46034977 | ACAGAGTTAGCCTAC[C/T]GTAGTTAAAAATGAA | 51317 |
rs756189644 | snp | A/C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46116057 | ATTTAAGATACTATA[A/C/T]CTTTTGATAGGCTCA | 51317 |
rs756191238 | snp | G/T | 3.46045e-05 | 0.00415945 | intron-variant | PHF21A | GRCh38.p7 | 11:45953497 | CCATACACCATAGAC[G/T]GAGACCTGCCTTTGG | 51317 |
rs756203063 | snp | G/T | 1.64923e-05 | 0.00287156 | missense, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45938276 | GTAACTGGCCACTTT[G/T]TCTGCAAACGCTGCA | 51317 |
rs756204583 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45973154 | AAAACAAAATTAAAA[C/T]ATCAGCTCCTCAGTT | 51317 |
rs756206692 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46114570 | CTTCGTCAATACAAC[A/G]TACTGTCCATAAGGC | 51317 |
rs756225383 | in-del | -/TG | | | intron-variant | PHF21A | GRCh38.p7 | 11:46021548 | ATGTGTGTGTGCATG[-/TG]TGTGTGTGTGTTCAG | 51317 |
rs756234189 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46099900 | CCTGACTTTAGGCCT[-/A]AAAACTAAAAATGGT | 51317 |
rs756251608 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46075522 | GAATCACATTCAGAG[C/T]CAAATACATACTAAC | 51317 |
rs756251798 | snp | C/G | | | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45929392 | TCAGCTGCTCTGTAT[C/G]CCCCCCCACCCCCTC | 51317 |
rs756276994 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46062141 | CTTTTATTCTTGTTT[G/T]GCTAAAGTTTCACCA | 51317 |
rs756280111 | in-del | -/AAAC | | | intron-variant | PHF21A | GRCh38.p7 | 11:45985909 | TTATATAGTACAAAT[-/AAAC]AAATTGACAACAGCA | 51317 |
rs756289319 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45950698 | ACATCTTCTTTCTCA[A/G]TGACAGAAATCAGTA | 51317 |
rs756309278 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46026017 | ACAATGTCCCAAGAA[C/T]GTCCTTTAAGTAAAA | 51317 |
rs756337280 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46112191 | GAGAAACTGAGGTGC[-/A]AGGACATTTTACACA | 51317 |
rs756363310 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45971669 | AATGGGGTAGGTATA[C/G]AGATACAGAATGTGA | 51317 |
rs756366730 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46060919 | GTATTGCTGAGGTTA[C/T]CTACCAGGGTTTTTA | 51317 |
rs756369283 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45983067 | AACAGAAGGGAACAG[C/T]AGGGAAAGCAGGAGC | 51317 |
rs756375264 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46103874 | TACTGGTTTCACTTA[C/T]AAGATAGAGACATTC | 51317 |
rs756397279 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46024810 | ATCTCAAAAAAAAGA[A/T]AGAAAGAAAGAAAGA | 51317 |
rs756406620 | in-del | -/ATG | | | intron-variant | PHF21A | GRCh38.p7 | 11:46029100 | AGAGTGTTATCTGTC[-/ATG]ATAAGCTAAACCTTG | 51317 |
rs756408471 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46073950 | TGAAATTCACTGAGT[G/T]TTAGTCATGAAGGAT | 51317 |
rs756420499 | in-del | -/GTA | 1.64822e-05 | 0.00287068 | cds-indel, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45979834 | ACTGCTGCTGTTGTT[-/GTA]GTTGCTGTAGTGGTT | 51317 |
rs756441738 | snp | A/T | 1.73921e-05 | 0.00294885 | intron-variant | PHF21A | GRCh38.p7 | 11:45934271 | AGCCGCCTGGTTTCT[A/T]ACAGGCCTGGCAGCC | 51317 |
rs756455768 | snp | C/T | 1.6489e-05 | 0.00287128 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:46084184 | GTGAACCTGAATTTC[C/T]ACTTTAAGAGCCTCC | 51317 |
rs756470160 | snp | A/C | | | upstream-variant-2KB | PHF21A, LOC105376661 | GRCh38.p7 | 11:46123119 | CCATAGGCATGAAAT[A/C]CAGTTTTTGCAGATA | 51317 |
rs756473894 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45948559 | TGTTCTGCTTAATGA[C/T]TCTCAAATGCTTCCT | 51317 |
rs756482917 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46037919 | AGGATCGCTTTTCTT[C/T]TGAAGCTCCTACTAT | 51317 |
rs756500520 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46091023 | TGATTATTTATTTTA[A/C]AAGGTTTAATGAGAG | 51317 |
rs756509314 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46009115 | GAGTAGCTGGGATTA[C/T]AGGCGTGCATCACCA | 51317 |
rs756514838 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46053163 | TAGAAGTTGATTTAG[C/T]GTCCTGATAAATGTT | 51317 |
rs756528773 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46034495 | TCCACACTCCAAGAT[-/A]AAAAAGAACAAAAAA | 51317 |
rs756530288 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45936873 | AACCACTCCCGACAG[C/T]TAGAACCACCAACAC | 51317 |
rs756566365 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46016858 | AAATTAAACAGACAC[A/G]ACCTCAACCAATGAT | 51317 |
rs756589458 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46001688 | AGAAAGGCTGTGTGC[A/C]TCAGAGTTAACTGGT | 51317 |
rs756595582 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46005764 | AATTAAGCTTCCATA[A/G]CTCAAGACGGATCAT | 51317 |
rs756616581 | snp | C/T | 1.64746e-05 | 0.00287002 | intron-variant | PHF21A | GRCh38.p7 | 11:45948871 | AGCAAGGGAGAGATA[C/T]AAAAAGGTCCTCACC | 51317 |
rs756619564 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46065827 | ACAGAGGCTCACAAT[A/C]TAGAGAGGAAGAAAT | 51317 |
rs756620205 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45937949 | TTTCAAATACAAGGA[A/G]GCATCTATCCAGCTC | 51317 |
rs756624123 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45963718 | ATAATATTTAATAAC[C/G]TAAAATAGTGTTGTG | 51317 |
rs756641322 | snp | C/G/T | 8.23676e-05 | 0.00641693 | intron-variant | PHF21A | GRCh38.p7 | 11:45949374 | AAACTGGAACATGAG[C/G/T]GAAGGGCCAGATGCT | 51317 |
rs756653683 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46018949 | TCAATGTATCATACC[A/G]TAAGCAGCAAGAACA | 51317 |
rs756679419 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46000167 | GAAGGCAGCAAACTA[C/T]AGAGAAGAAACCAAC | 51317 |
rs756707290 | snp | A/C | 1.64955e-05 | 0.00287184 | missense, stop-gained, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934184 | GGAGCTGTGCATCTC[A/C]TTCTGCCGGGCCAGG | 51317 |
rs756716094 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45965713 | TGTTTAATACACTTA[C/T]TAATGTTCATTTTGG | 51317 |
rs756734220 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46002034 | TTTCATGAGAAAATA[C/T]AAAGAAAAGAGTGAC | 51317 |
rs756764746 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46105765 | AAAAAGCACTAGGCC[A/T]CTTTGAAAGACTCAA | 51317 |
rs756772849 | snp | A/G | 1.64738e-05 | 0.00286995 | intron-variant | PHF21A | GRCh38.p7 | 11:45949379 | GGAACATGAGGGAAG[A/G]GCCAGATGCTGGCCA | 51317 |
rs756837246 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46067910 | CACAGAAGAGGAGTG[G/T]CTAACTCTGCTTGGA | 51317 |
rs756844656 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45979358 | TCTATCTGGTCCCAA[G/T]AGCACTGATCCTGGA | 51317 |
rs756882574 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45939266 | TAAATCTTACAGGTA[C/T]GGAAATCCATTCATC | 51317 |
rs756912783 | in-del | -/AT | | | intron-variant | PHF21A | GRCh38.p7 | 11:45989240 | AGAATTTCAGAACAC[-/AT]ATTTGCTTTTGTTTG | 51317 |
rs756916296 | snp | C/T | 3.29544e-05 | 0.00405908 | missense, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45971295 | CCACAGAGGCAGGCA[C/T]GGTCGCAGTTGCTGC | 51317 |
rs756924104 | snp | A/G | | | intron-variant, downstream-variant-500B | PHF21A | GRCh38.p7 | 11:45934862 | TTTTAGGCAGGGAAA[A/G]AGAGGAAAGAGGTGT | 51317 |
rs756928809 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46066193 | GGTAACAAAGGTAGT[C/T]TCTCTGGTAGAGGAG | 51317 |
rs756930892 | snp | C/G | 1.75551e-05 | 0.00296264 | downstream-variant-500B, missense, utr-variant-3-prime | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45928832 | AGCAGCCCCAGAGCC[C/G]TGCCCGAGGCTGAGG | 51317 |
rs756935067 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46088139 | GCATCAAAAGAATTA[C/T]TGGCTACATTTGTAA | 51317 |
rs756967811 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45996298 | GTACTCAAGGTAGTA[A/G]AGCTTACAGGTTGAC | 51317 |
rs756971060 | snp | A/G | 3.29457e-05 | 0.00405854 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45948895 | CCTCACCTCTCTTCC[A/G]GGTCCCAGGGTGCAT | 51317 |
rs756972612 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45955438 | TGAATAGGAAGGAGA[A/G]AAGTATGATGGAGGA | 51317 |
rs756974830 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46044552 | ATGCAGGACTTCTCT[C/T]ACTCTTTCGGGCAAC | 51317 |
rs756979639 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46097993 | TAGATCTGTATTTAA[C/G]TTCCCCCAAAAGATT | 51317 |
rs757025201 | snp | C/G | | | upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46122594 | GCAATCACTGGGAAT[C/G]GGCCACGTATAATCC | 51317 |
rs757051738 | in-del | -/AC | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PHF21A | GRCh38.p7 | 11:45933136 | TTTTTTCCTTCCTGG[-/AC]ACACACATCCTTCTT | 51317 |
rs757060658 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46043380 | GTTTACCCACATCAT[C/G]ACCTTTATCAATACA | 51317 |
rs757078384 | snp | C/T | 1.71402e-05 | 0.00292742 | intron-variant | PHF21A | GRCh38.p7 | 11:45938121 | CCGTGTCTTTGTCCT[C/T]CTCGGCCCCTCCCCT | 51317 |
rs757083488 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45956014 | GAAGGAAATGGGTTA[A/C]TATATTTAAAGTGCT | 51317 |
rs757113475 | snp | C/T | 3.28294e-05 | 0.00405137 | intron-variant | PHF21A | GRCh38.p7 | 11:45953667 | TCAGAATTCGTTTTT[C/T]ATTAAAAGGATGAAG | 51317 |
rs757135512 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45953987 | CCCAGAAGCAAGCCT[A/G]CTATTTTTTGTTGTT | 51317 |
rs757144111 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46024142 | AATGATTTTATATGT[G/T]GGGCTAACTGAGTTG | 51317 |
rs757166311 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46058840 | CTAGAATGGAGAAGA[C/T]ACAAACATGGGAACT | 51317 |
rs757184850 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45934495 | ACACAGGAGTACTAA[C/T]GCTTAAAAACAAACC | 51317 |
rs757202768 | in-del | -/CT | | | intron-variant | PHF21A | GRCh38.p7 | 11:46027168 | AGCTGTCTCACATCA[-/CT]CTGCTTTTTCTCCCT | 51317 |
rs757237297 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46007001 | AGCATATGCCACACA[C/T]TTCACAGTTTTAATC | 51317 |
rs757243048 | in-del | -/TAA | | | intron-variant | PHF21A | GRCh38.p7 | 11:46095678 | TAAATCTAAAGCAAT[-/TAA]TAATTATTTAAATAC | 51317 |
rs757254710 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45943367 | AATGTTTTGTAGAGA[C/T]AGGGGTCTTGCCATG | 51317 |
rs757254970 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46014989 | CGTCTCAAAAAAAAA[A/T]AAAAATAAAAATAAA | 51317 |
rs757274628 | snp | G/T | 1.69355e-05 | 0.00290989 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45965352 | CTAAGCTGTACAGTT[G/T]GAGGTCCAGCGAGTC | 51317 |
rs757281216 | snp | A/G | | | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46084582 | ATCACTACATACTGA[A/G]GATACAGAGCTGAGT | 51317 |
rs757299379 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46048341 | TCATTCTATATGTAG[C/T]ACTTCATTCCTTTTT | 51317 |
rs757328685 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46023268 | AGGCAGGCCGGGATC[C/T]GGCAGAGAGACAGCT | 51317 |
rs757331516 | in-del | -/TTTA | | | intron-variant | PHF21A | GRCh38.p7 | 11:46059895 | CCACGCCCAGCTGAT[-/TTTA]TTTATTTATTTTTGG | 51317 |
rs757343295 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45960117 | CTGTGGAAAACAGTT[C/T]GGCAGTTCTTCAAAT | 51317 |
rs757357943 | in-del | -/AAAAAAAAAAA | | | intron-variant | PHF21A | GRCh38.p7 | 11:45968932 | GCGAAACTCCATTGC[-/AAAAAAAAAAA]AAAAAAAAAAAAAAA | 51317 |
rs757366978 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45997699 | AGACAAAAGCCAATC[C/T]ACCTGTTCAGGATCT | 51317 |
rs757368931 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46012820 | CTCATCTTAATGATA[C/T]CCTAAGAGCTCATGC | 51317 |
rs757370110 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46063026 | GATGACGGTTTCACA[C/T]CATCAAAAATTACTC | 51317 |
rs757392692 | snp | A/C/G | 1.65343e-05 | 0.00287521 | synonymous-codon, missense, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45938295 | GCAAACGCTGCAAAA[A/C/G]TCCTCATGAATATCA | 51317 |
rs757404448 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46101784 | GGGACTACAGGCACA[C/T]GCCACCACACTCGGC | 51317 |
rs757419575 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45941904 | TTCTCATAAAAATGA[C/T]GATAGTGGCAACACG | 51317 |
rs757421257 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46048536 | GCAATTTGGGAGGCC[A/G]AGGCAGGCAGGTCAC | 51317 |
rs757457001 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46011539 | TGAAGTAAGAAGATT[A/G]GCAATTTCTAAGATA | 51317 |
rs757460674 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46046837 | TTTCCAAACACTGAT[C/G]AAGGATTTCTCCCAT | 51317 |
rs757509961 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46076958 | CTGTCATGCATTACA[C/T]TGTGGCCATAATACC | 51317 |
rs757521460 | snp | C/T | 2.48821e-05 | 0.0035271 | intron-variant | PHF21A | GRCh38.p7 | 11:45965639 | AGAATAATTATTGTA[C/T]TACTTAAGCTGCTCA | 51317 |
rs757528655 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45938003 | AGGGAATGAAGGCCA[A/T]GCGCCTGCGTGCTGT | 51317 |
rs757558015 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45974655 | AGACGTGATCTCGCT[A/G]TGTTGCCCAGGCTGG | 51317 |
rs757559060 | snp | C/G | 1.66405e-05 | 0.00288443 | missense, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45945875 | GCAGGGACACAGGCT[C/G]AACAGGTGCAGGGAA | 51317 |
rs757575641 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46027051 | ACACGCACACATGCA[C/T]GCAAATCATCATTCC | 51317 |
rs757575884 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46001848 | GGATGGAGGTCTTTG[C/G]TTTCTATGACAACCC | 51317 |
rs757588650 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46116309 | TAACACATACAGATA[C/T]ACATCTTTTTCACTG | 51317 |
rs757625314 | in-del | -/TCA | | | intron-variant | PHF21A | GRCh38.p7 | 11:46117750 | TGCTCAACATCCCAC[-/TCA]TCAACACAAGACTAA | 51317 |
rs757651374 | in-del | -/AA | | | intron-variant | PHF21A | GRCh38.p7 | 11:46021061 | TTAGATAGATTCTTT[-/AA]AAAAAAAAAAAAAAG | 51317 |
rs757665102 | in-del | -/AGGAA | | | intron-variant | PHF21A | GRCh38.p7 | 11:46079856 | GAAAGGAAAGAGGAA[-/AGGAA]AGGAAAGGAAAGGAA | 51317 |
rs757677355 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46038864 | TCACCTCTTAAAGGC[C/T]CCATCTTTCAGTGCT | 51317 |
rs757688136 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45950045 | GGAACATTAGACAGA[A/G]GGAAGGCAATTTTCC | 51317 |
rs757690659 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46092139 | TAACTATCCAGCTAG[C/T]ATCAGGATCAGGCAC | 51317 |
rs757704513 | in-del | -/AA | | | intron-variant | PHF21A | GRCh38.p7 | 11:46027014 | CTTTTCTGAAAAATT[-/AA]AAGTCTGAGAGCAGG | 51317 |
rs757704940 | in-del | -/CTTT | | | intron-variant | PHF21A | GRCh38.p7 | 11:45945109 | GACATTATATATTCA[-/CTTT]CTTATTATCTGCCTC | 51317 |
rs757715634 | in-del | -/GTG | 0.000181821 | 0.00953297 | cds-indel, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45979805 | AGCTGACTGCTGGGC[-/GTG]GTGGTGGTGGTACTG | 51317 |
rs757722328 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46107268 | GTCAAGATGACTGAG[A/T]CTAGAATAAAAAAGG | 51317 |
rs757722963 | snp | G/T | 0.000185512 | 0.00962919 | intron-variant, downstream-variant-500B | PHF21A | GRCh38.p7 | 11:45935093 | ACCCTCTTTCCCACT[G/T]GGACAGGCCGGGCTG | 51317 |
rs757723103 | snp | C/G | 1.65954e-05 | 0.00288053 | intron-variant | PHF21A | GRCh38.p7 | 11:45950160 | ATTTTCAGGAACAAA[C/G]CTGTGGGCCAGAAAA | 51317 |
rs757723511 | snp | A/G | 1.7586e-05 | 0.00296524 | synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45965528 | CATGACGGGCCTCTG[A/G]ATAAGCTGAGGAGCT | 51317 |
rs757776350 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45948741 | CTCATTCTCTTTTCT[C/T]TCCCATTCTCAGAGA | 51317 |
rs757787438 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46083978 | GAAAGGAAGTCAGGA[A/C]TACTTTAAGTTCTTA | 51317 |
rs757810876 | snp | C/T | 3.71975e-05 | 0.00431247 | intron-variant | PHF21A | GRCh38.p7 | 11:45935559 | AGCCTGGGGCCCACA[C/T]GTACTGTTACGTATA | 51317 |
rs757811418 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46054880 | AGCTCTTTTAACCAG[G/T]AACGACTAGGACCAG | 51317 |
rs757834075 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45987553 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 51317 |
rs757843526 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46005107 | GCAGGCTCAGTTACC[A/G]AGAGCAACCGCAGTC | 51317 |
rs757845246 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46068136 | TGAGTTGCTAAAGGT[A/G]TCAGTGCTAATGAGC | 51317 |
rs757882610 | snp | A/G | | | intron-variant, missense, utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45935147 | GTCTCTAGAAAGCCC[A/G]CTTCCTCACACTGGT | 51317 |
rs757905835 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45949247 | GTAAGCAGTGACTAA[C/T]AAAAATGATAAGTCA | 51317 |
rs757920963 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46092347 | ACACACACAAGTTTC[A/C]AAAGTTTTAAAACCC | 51317 |
rs757926860 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46055162 | AGCAATCTGAATGTA[A/G]AATCCTTCTGGACAT | 51317 |
rs757931397 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46020636 | ATGAAATTTCTCAAA[C/T]ATGAACATGACCCAG | 51317 |
rs757931748 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46003593 | GCAGAGTGAGAAAAC[A/G]CTACAATTCTCACTA | 51317 |
rs757953113 | snp | A/G | 3.29511e-05 | 0.00405887 | missense, utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45979881 | TGTAGTTTGTTTTCA[A/G]ATTGTGGCAATGGCT | 51317 |
rs757957802 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46082186 | ACACAAAGAACAAAA[A/C]TATGTTTTCACTCCA | 51317 |
rs757992048 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45998336 | TGTGAAAGGATGTTA[A/G]GGCCATGGATAGAGT | 51317 |
rs757993851 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45965832 | TTGATTCTAAACCCT[C/G]AGCTCCCTCTTCTAT | 51317 |
rs758008933 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46107360 | ATTAATTGAGCCCTC[G/T]GTACACTATTAGACT | 51317 |
rs758013620 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46117637 | CTACTCTATATCCTA[C/T]TTGTATTAATATTAT | 51317 |
rs758033188 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46068927 | TGCCCTATAATAATG[C/T]GGCACGTTATTAAAG | 51317 |
rs758049202 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46033160 | TATACCTGCAGTTCA[C/T]TCATTTTTTAAAAAC | 51317 |
rs758098969 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46083820 | CATATGGTAGTTGAG[A/T]TAGACATGTTGTTAT | 51317 |
rs758113439 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46017093 | CTCCTGCCTCAGCCT[C/T]CTGAGTTGCTGGGAT | 51317 |
rs758138972 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46046476 | AGAAACCAGAGCTCG[C/T]CATACAGGGCAAGAG | 51317 |
rs758151377 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:45988580 | ATAGCACAGGCACAT[-/A]AATTTTAAAAGATTC | 51317 |
rs758152527 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45986672 | TCAGAAAAATATTGG[C/G]AATCAAATTAATTAA | 51317 |
rs758173258 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46114675 | TACTTATTTAAAATT[A/T]AAAAAAAACACACAC | 51317 |
rs758180407 | in-del | -/TGTCA | | | intron-variant | PHF21A | GRCh38.p7 | 11:45985319 | GAGGGGATGTGTTAC[-/TGTCA]TAACATTAGAGACAA | 51317 |
rs758211324 | in-del | -/ATT | | | intron-variant | PHF21A | GRCh38.p7 | 11:45974422 | GTCAAACGACAAATT[-/ATT]ATTATTATTATTATT | 51317 |
rs758222202 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45979422 | AGAGGTCAAGTCACA[A/G]ACTTTTAGAACAAGT | 51317 |
rs758223283 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46031949 | CACAGTTACCCAATT[C/T]TCCCCAATGCACATC | 51317 |
rs758254725 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45957870 | AAAGAATAACAAAAT[C/T]GACAAACCTCTGGCT | 51317 |
rs758262888 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46098547 | CTCTATAAAGTACAA[A/C]AATCCTTATTCACAA | 51317 |
rs758290521 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45929696 | AGGGCCTTGTGGGAG[A/G]GGGCGCCAAGTGGAA | 51317 |
rs758291150 | snp | A/G | 3.4239e-05 | 0.00413743 | intron-variant | PHF21A | GRCh38.p7 | 11:45938125 | GTCTTTGTCCTCCTC[A/G]GCCCCTCCCCTGTTG | 51317 |
rs758308941 | snp | A/G | 7.12441e-05 | 0.005968 | downstream-variant-500B, missense, utr-variant-3-prime | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45928838 | CCCAGAGCCCTGCCC[A/G]AGGCTGAGGCTGGGC | 51317 |
rs758309805 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46020382 | CACCAAGAACCAGGA[A/G]CGCCTGCTCTGACAC | 51317 |
rs758313325 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46044921 | AAAAGATAGGAACTG[A/T]TCGAAGCTTTCAAAG | 51317 |
rs758354504 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46097227 | TCAAAATCCAAGACA[G/T]ATCTTGTTACTCCTC | 51317 |
rs758378001 | snp | C/T | 1.6477e-05 | 0.00287024 | missense, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45938251 | ACACGGGAACATGTG[C/T]CGCACATCAGTAACT | 51317 |
rs758394838 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46070859 | ATAAGCATCAAATGC[A/G]TATCAATACATCTTC | 51317 |
rs758404327 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46093926 | TACCATTTTAAAATA[C/T]AGTAAAAAGGAAAAG | 51317 |
rs758426743 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45984993 | AGAGGCTGATAGAGA[C/G]TTGTAACTTTTCACA | 51317 |
rs758433365 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45968490 | TTTCTCCACCCTGGA[A/G]CTACATACATGTTCT | 51317 |
rs758498400 | snp | C/T | 3.50287e-05 | 0.00418487 | intron-variant | PHF21A | GRCh38.p7 | 11:46076887 | ATAGTAGCAGGAAGA[C/T]TATGCATACTGCATT | 51317 |
rs758501208 | snp | A/G | 1.75194e-05 | 0.00295963 | missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934002 | TGGTTACAGTTCGCT[A/G]TGCAGCTCTGGGAGG | 51317 |
rs758505446 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46049977 | AATCAAAGTAGGACC[A/G]TATTCTATCATATAT | 51317 |
rs758514555 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45983551 | ATGCCCTCTGTCACT[G/T]AAATATAGATGACTG | 51317 |
rs758515015 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46013233 | TGGCATAGGCACTGT[-/G]AATAGAAAATTCCAG | 51317 |
rs758537875 | snp | A/T | | | intron-variant, utr-variant-5-prime | PHF21A | GRCh38.p7 | 11:46088586 | GTGTGACTACTCTCA[A/T]CCCCAGGGTTCATTT | 51317 |
rs758618164 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45944919 | TTACAGGAGCACGCC[A/G]TGCCCGGCTAATTTT | 51317 |
rs758618899 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46035047 | ATGAGGACTGAAGAG[A/G]TTTGCTGCTTCTTGC | 51317 |
rs758619255 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46077255 | TTTTCTCCACTTGCC[C/T]TCTCCCTTATTTAGC | 51317 |
rs758634582 | in-del | -/CAGT | | | intron-variant | PHF21A | GRCh38.p7 | 11:45953346 | GGACCCTCAAGACTA[-/CAGT]CTAAGAATTCCACTC | 51317 |
rs758640476 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45959661 | ATCCATAAAACAAAT[A/G]CTAGAGCTAATAAAC | 51317 |
rs758653240 | snp | A/G | 1.64768e-05 | 0.00287021 | intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45946027 | CAAGAGAAGGGAACA[A/G]AAGGGAAAAACGGGG | 51317 |
rs758671691 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46009701 | AGCCAGAGCAGACTT[A/C]CAACTTGGGCAGTTT | 51317 |
rs758673710 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46042595 | TCTTATGACTAGGAC[A/C]TGGTGCTAGATCTGA | 51317 |
rs758683143 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46064515 | GGAGTAAATCAACTT[C/T]GGGAAACATATCTTC | 51317 |
rs758708353 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45943538 | GGTCTTCCTGCTTCC[A/G]TCCTATTTTCCCTAT | 51317 |
rs758708504 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45961354 | TTAGTCAAGGTTAAA[C/T]AGATTGGGATTGAAG | 51317 |
rs758711545 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46011708 | CTTTCAAGCAATGTA[C/T]TTAGCTAACAAAAGT | 51317 |
rs758714241 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46102025 | ACCACGCCCAGCTAA[C/T]TTTTGTATTTTTAGT | 51317 |
rs758716021 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46067335 | TGAGTTCAATGGGGA[A/G]GCGGGCATGAGTGAG | 51317 |
rs758721117 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46013264 | AAAAAATAATCCATA[A/G]GTTTTAAACTGCACG | 51317 |
rs758744210 | in-del | -/TGT | | | intron-variant | PHF21A | GRCh38.p7 | 11:45961639 | TCTGAATTGACGACA[-/TGT]TGTTACATAGAAGTC | 51317 |
rs758750469 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46116482 | TAAAATCAACTACTA[A/T]CACATCACATCAATG | 51317 |
rs758764795 | in-del | -/AGAA | | | intron-variant | PHF21A | GRCh38.p7 | 11:46098507 | ATAGCAGAAATAAAT[-/AGAA]AGAAGAAATCTTGCT | 51317 |
rs758765300 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46040255 | CATAATGGTCTCACC[C/T]CAGTGGAAAAGAGAG | 51317 |
rs758773216 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46078576 | AAAGAAAAGTTAACA[C/T]TCTCTGTTAATTTTT | 51317 |
rs758826006 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45981516 | AGCATATAATAACTA[C/T]TTGGGGCCATATTTG | 51317 |
rs758845364 | snp | A/G | 2.63376e-05 | 0.00362879 | intron-variant | PHF21A | GRCh38.p7 | 11:45969933 | AAGATAAATAAACCA[A/G]AGAGAACAATTACTC | 51317 |
rs758845514 | snp | G/T | 3.31148e-05 | 0.00406894 | missense, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45945901 | GGGAAAGTGAATGTG[G/T]TCTCTGTCTTTTCAT | 51317 |
rs758855518 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46028811 | ACTCCTGACCTCATC[A/G]TCCACTCGCCTCGGC | 51317 |
rs758872460 | in-del | -/TGATTTTA | | | intron-variant | PHF21A | GRCh38.p7 | 11:45940661 | TCCTTCATTATTAAA[-/TGATTTTA]ATCAGGCTGAGGGCT | 51317 |
rs758888131 | snp | C/T | 1.64819e-05 | 0.00287066 | synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45935675 | CACCTTTTGCTCTAG[C/T]TGTTCTCGTTCTTGT | 51317 |
rs758923722 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46091623 | AATTTCAAAGTCAAG[C/T]TTCCACAGTTAAATT | 51317 |
rs758924849 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46007975 | TCTTTTTCTGTCTGT[A/C]CTTGGGATTACCATG | 51317 |
rs758943466 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45973536 | CTTAAATGTGAAATG[A/C]GAGTAAACGCGGAAC | 51317 |
rs758957915 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45978310 | CGTCTCAAAAAAACA[A/G]TAACAAAAAAACAAA | 51317 |
rs758998545 | in-del | -/ATAAT | | | intron-variant | PHF21A | GRCh38.p7 | 11:46008708 | AATAAAAGGAAAATA[-/ATAAT]ATATGTTTTACATAT | 51317 |
rs759030034 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46040603 | AATACAATCTAGTGC[A/C]CCAAAAATAACAGTA | 51317 |
rs759043116 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46109778 | TTGAGATCAGGAGTT[-/A]AGAGACCAGTCTACC | 51317 |
rs759049610 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46069067 | AAAGGAGAGCAGATA[A/G]TACAGCACTGGGAAC | 51317 |
rs759050993 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46072890 | TTAAGATTGCCTCTA[A/C]AAGAAAGCAAAATGA | 51317 |
rs759087625 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45970629 | CTGACACGGTTAATT[G/T]GTGAGTTTCTTGAAT | 51317 |
rs759093524 | in-del | -/AGC | 1.69186e-05 | 0.00290844 | intron-variant | PHF21A | GRCh38.p7 | 11:45971098 | TGATCACACATGAGG[-/AGC]AGCAGCTGCTGGCTT | 51317 |
rs759108775 | in-del | -/AG | | | intron-variant | PHF21A | GRCh38.p7 | 11:46024902 | ACCATAGTGACTCCT[-/AG]AGTTCTAGACTAGTC | 51317 |
rs759114228 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46112069 | TCTGAAGTCAACCAA[A/G]GGCTTGTGGTATGGA | 51317 |
rs759120687 | snp | C/T | 1.64961e-05 | 0.00287189 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934126 | CAGGTTTGGAGAGGT[C/T]GATGCCGTGGATGAG | 51317 |
rs759122878 | in-del | -/ACT | | | intron-variant | PHF21A | GRCh38.p7 | 11:46032496 | TTTTTTCAATTCTCC[-/ACT]ATTATTTAAAAAAAC | 51317 |
rs759126173 | snp | A/T | 0.000258904 | 0.0113748 | synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45965339 | AAGACTTGGCTTGCT[A/T]AGCTGTACAGTTTGA | 51317 |
rs759165496 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46102144 | TACAGGCGCGAGCCA[A/C]CACGCCTGTCCCTGT | 51317 |
rs759178517 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46074461 | GGCTCTTTTGGCGGG[-/A]AGGGGGGAAGGCATA | 51317 |
rs759183848 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45944011 | AGACTGAGAAACTCT[A/T]CCAAAATAAAGGATT | 51317 |
rs759220764 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45946256 | TGACAGAAGGTGCTG[A/G]CTTATGTAGAAAGAC | 51317 |
rs759229225 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46088214 | AACAAATCAGTTGCT[C/G]CAAAGTGAATACCAT | 51317 |
rs759235526 | snp | A/G | 1.6543e-05 | 0.00287597 | intron-variant, stop-gained, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:46076822 | TTAAGTCAGCATTCT[A/G]ATTGGAAAGAAAAAA | 51317 |
rs759247970 | snp | A/G | 3.35745e-05 | 0.00409709 | intron-variant, synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45946085 | ACATACCTTTGGCCA[A/G]TGTTCCTCATTGGCT | 51317 |
rs759250089 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46099659 | CCTAGAAAACTCAGA[-/G]TAGGCCTTACCGAAG | 51317 |
rs759310849 | snp | C/T | 1.662e-05 | 0.00288266 | missense, utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934051 | TGGAGGTGGCGGCAT[C/T]GGCAGGGGGGGTGCA | 51317 |
rs759316955 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46086394 | AAAGTGCTGGGATTA[C/T]AGGCATGAGCCACCG | 51317 |
rs759318478 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45961029 | TCAATTATTATCATG[C/T]TTGTCTTACTTATTA | 51317 |
rs759323487 | snp | A/G | 1.69413e-05 | 0.00291039 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45953613 | CATCTGTTTCTGTGT[A/G]AGATTTAACTGTCTA | 51317 |
rs759328442 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46101280 | GACAAATGAAAATAT[C/T]ATCCTAAAAGGGATT | 51317 |
rs759338087 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46035651 | CTAATCTATAGGTCA[A/G]AGAAGGCCTCTAGGA | 51317 |
rs759369474 | snp | A/C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46063989 | AAATAAAATCACATA[A/C/T]TCAGAAAAACAAATT | 51317 |
rs759410662 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46117227 | AAGCAGATTTATCAA[A/G]CTTTCTAGCATCCCC | 51317 |
rs759427728 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46049548 | TAGAAGAGGGTGTGG[C/T]GGGGGAAGGAGGGAT | 51317 |
rs759448601 | snp | A/T | | | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46118865 | TCTTCAAAGACCAAA[A/T]GCAAAGCTGACCTAT | 51317 |
rs759468297 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46029494 | GGAGTTCAAGACCAG[C/T]CTGGGCAACATGGTG | 51317 |
rs759481559 | snp | A/G | 2.04975e-05 | 0.0032013 | intron-variant | PHF21A | GRCh38.p7 | 11:45969907 | TTGCCTGAACCTGCT[A/G]AAAAATGAGGAAGAT | 51317 |
rs759482092 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46112857 | AAAGAGACCTGTATC[A/G]CCACATGCATAAAAA | 51317 |
rs759521447 | snp | C/T | 3.29571e-05 | 0.00405924 | missense, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45945985 | AACCCCAGCACTGCA[C/T]TGTATTTTGGAGGAC | 51317 |
rs759543941 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46039807 | CTAGAGTCCTTGACT[A/G]AAGTCAGAGGAAATA | 51317 |
rs759635538 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46054589 | TGAGAACCAGCAGTT[C/T]ACACGTAGATGTGGC | 51317 |
rs759639226 | snp | A/T | 1.64817e-05 | 0.00287064 | missense, utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45979812 | TGCTGGGCGTGGTGG[A/T]GGTGGTACTGCTGCT | 51317 |
rs759642350 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46076694 | TCTCTTAGAAGCCTC[A/G]AGCAGACATATCTTT | 51317 |
rs759660221 | in-del | -/GA | | | intron-variant | PHF21A | GRCh38.p7 | 11:45996505 | ATGATTTCCCTTTTT[-/GA]GAGACAGAGAGAGAG | 51317 |
rs759687616 | snp | A/G | 0.000185546 | 0.00963009 | intron-variant, synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45935241 | TGGGCCCACTCGCTC[A/G]GGTGACTAGGAAGAA | 51317 |
rs759696677 | snp | A/G | | | synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45965327 | TACCTGTTTTTCAAG[A/G]CTTGGCTTGCTAAGC | 51317 |
rs759711538 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45932889 | AGCCTGAAAAACAGC[-/T]TTTTCTATTCCTTAT | 51317 |
rs759713354 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46100603 | CCTTGCACTAAATGA[C/T]AGATGCCAAATAACA | 51317 |
rs759723452 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46052705 | CTACCAGTTTTTCAC[C/G]ATGTGCCCTGGTGGA | 51317 |
rs759734384 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45966439 | TCTACTTCTATCCTC[A/T]CTCCACTATCTACTA | 51317 |
rs759738698 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46106549 | AGTTACAAAGTTTGG[C/T]CTTCGAGATATGATG | 51317 |
rs759770676 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:45939264 | ATAAATCTTACAGGT[-/A]ACGGAAATCCATTCA | 51317 |
rs759770799 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46026705 | GTGGGCTTTTAAATC[C/T]GTAATTAAAAAACCT | 51317 |
rs759783379 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46068526 | GAAGAGTCCCTAAAC[A/C]TTCTGAAATACAGAT | 51317 |
rs759810309 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45940863 | GGACTTGGGATAAAC[A/G]AAGAGGCGTTCACTT | 51317 |
rs759822074 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46063016 | TCTTGATCGTGATGA[C/T]GGTTTCACACCATCA | 51317 |
rs759831740 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46081472 | TAGAAGCTGAAAAAG[A/G]TTTTCTTCCAGACAC | 51317 |
rs759860613 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45928973 | AGCATCTGTGGGGTG[A/G]GGTCTTCCCCTTGCT | 51317 |
rs759873830 | snp | C/T | 1.71223e-05 | 0.00292589 | intron-variant | PHF21A | GRCh38.p7 | 11:45934251 | TGACAAGGGCAGTGG[C/T]ACTGAGCCGCCTGGT | 51317 |
rs759880723 | in-del | -/AAAGAATGCAT | | | intron-variant | PHF21A | GRCh38.p7 | 11:45985997 | TGTTTAACAGATGGC[-/AAAGAATGCAT]AAAGAATGCATATAT | 51317 |
rs759890140 | in-del | -/AAAAAA | | | intron-variant, cds-indel, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46119745 | GAACGTGGTCAGGGG[-/AAAAAA]AAAAAAAAGAAATCC | 51317 |
rs759924939 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46016757 | AGCCCACTACCTGGA[A/G]CTTGGCAGCCCTCAG | 51317 |
rs759948570 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930483 | CCCCAAAGGGCCTGA[C/T]AAGGAAGGAAGAAAT | 51317 |
rs759950446 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45995601 | TCCATTAACCTTCCA[C/T]ATGAGAGCTCCCCTG | 51317 |
rs759991160 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45962139 | AGTTCCGTGAGGGTA[C/T]GGGCTTTAGTTTATC | 51317 |
rs760024902 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45939046 | CACGTGTTAGCCAGG[A/T]TGGTCTCGATCTCCT | 51317 |
rs760027684 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46042752 | TATAAAAGAGGCCTA[C/T]GAAAGCTTGTTTTTC | 51317 |
rs760030594 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45964690 | AGAGGTCTTTCTGCT[A/G]CAGAACCTTCAAGTA | 51317 |
rs760038648 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45994062 | AATGCTGGAGCCAAC[C/T]CAACAAGAATGATAT | 51317 |
rs760049104 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46080190 | TTGAGACAGGGTCTT[A/G]CTCTGTCACCTAGGC | 51317 |
rs760084461 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46097554 | CTAAAACTATAATCA[C/G]AATTGTTCCGCTCCC | 51317 |
rs760087166 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46097828 | TCTCCCTAACTAGAA[C/T]ACACACACACACATA | 51317 |
rs760095965 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46009221 | TCAGGTAATCTGCCC[A/G]CCTCGGTCTCCCAAA | 51317 |
rs760113994 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46046281 | GTGCCAATAGCACTG[A/G]GGCCATCCTCCTATG | 51317 |
rs760127730 | in-del | -/TT | 7.01508e-05 | 0.00592203 | intron-variant | PHF21A | GRCh38.p7 | 11:45935574 | GTACTGTTACGTATA[-/TT]TTGGAAAGGCCTAGG | 51317 |
rs760145728 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45954957 | AGATCTTTGATTTTC[C/T]TTCCTGGCCACTTCC | 51317 |
rs760147167 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46059837 | ATTCAAGCAATTCTC[C/T]TGCCTCAGCCTCCCA | 51317 |
rs760172374 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46113756 | GCTTGAACCTGGGAG[A/G]TGGAGGCTGCAGTGA | 51317 |
rs760172996 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45972339 | TTATATGGCCTAAAC[A/T]TCTATCTGGAGATAG | 51317 |
rs760201937 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46044237 | GCTGTCCTATAGTAC[A/T]GCTAGAGGTACCTTT | 51317 |
rs760205715 | snp | A/C | 1.7098e-05 | 0.00292381 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45965342 | ACTTGGCTTGCTAAG[A/C]TGTACAGTTTGAGGT | 51317 |
rs760216920 | in-del | -/TCAG | | | intron-variant | PHF21A | GRCh38.p7 | 11:45966335 | CCTCCGATAATTGCC[-/TCAG]TAAGTACCCTTTTCT | 51317 |
rs760217972 | snp | A/G | | | intron-variant, utr-variant-5-prime | PHF21A | GRCh38.p7 | 11:46075087 | ATGCAAACTTAGTTC[A/G]GAGAACAATTAGAGC | 51317 |
rs760224018 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46095323 | ATGCAAGTTTGATTT[C/T]TTCATGTTAAGCTGG | 51317 |
rs760244246 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46014482 | GAACATACAAGTGCA[A/T]GTGTACTTTTTGGTA | 51317 |
rs760258324 | snp | G/T | 1.64844e-05 | 0.00287087 | missense, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45938213 | TTGTTTTCAGAGGGG[G/T]GTCTAAGCAGTCCAA | 51317 |
rs760258671 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46046340 | AAGGGAAACCCACTT[C/T]TGGAGGCAAAAAAAG | 51317 |
rs760296152 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46060008 | CTCGGCCTCCAAAGC[A/G]CTGGGATTACAGGCG | 51317 |
rs760308964 | in-del | -/ATAA | 2.27234e-05 | 0.00337064 | intron-variant | PHF21A | GRCh38.p7 | 11:45969921 | TAAAAAATGAGGAAG[-/ATAA]ATAAACCAGAGAGAA | 51317 |
rs760320447 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45977417 | GTTGGGATTACAGGC[A/G]TGTGCCACTGTGCCT | 51317 |
rs760331775 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45955203 | TACTTCATGCAGAGC[A/G]GGTGTATAGTAAAGA | 51317 |
rs760337436 | snp | C/T | 1.67075e-05 | 0.00289023 | utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:46084266 | TATAGTTTCTTCAGC[C/T]TCTGTTTAAAGTAAC | 51317 |
rs760372163 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46008222 | TCCTAGACTAATCCA[C/T]AATGTTCAGATGATA | 51317 |
rs760373236 | snp | C/T | 1.69427e-05 | 0.00291051 | intron-variant | PHF21A | GRCh38.p7 | 11:45934239 | TTCTGCAGCAAATGA[C/T]AAGGGCAGTGGCACT | 51317 |
rs760379463 | in-del | -/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46024183 | TTCTTTCTCCTCCTT[-/C]CCATCACAACCTGAT | 51317 |
rs760388967 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46025327 | GTCCCTTTCACACAA[C/T]ATGACCAATAGGAAA | 51317 |
rs760405638 | snp | A/G | 1.651e-05 | 0.0028731 | intron-variant | PHF21A | GRCh38.p7 | 11:46079193 | GAGAGAAAAAGAGCC[A/G]TCAGTCTTACATATT | 51317 |
rs760425502 | snp | A/G | 3.31066e-05 | 0.00406844 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45965455 | GCCCATTGACGACAC[A/G]GACGGGGTGGATGGA | 51317 |
rs760438510 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45984696 | ACCAGTTTATTCCTA[C/T]CAAAAATTGCTCCCA | 51317 |
rs760451046 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45934468 | AGGGAGAAAGAGCAT[A/G]CGGGCACCAACACAC | 51317 |
rs760454574 | snp | C/T | 8.74669e-05 | 0.00661255 | intron-variant | PHF21A | GRCh38.p7 | 11:45938109 | TCCTCCTGATGGCCG[C/T]GTCTTTGTCCTCCTC | 51317 |
rs760480418 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45985923 | TAAACAAATTGACAA[C/G]AGCAGCAACTGTAAT | 51317 |
rs760485812 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46088361 | TGCAATCTTCCAAAC[A/G]GTACATGTCAAACCA | 51317 |
rs760489313 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46024096 | AAAGCAAGGAAAGGG[A/C]AAGGTGGTGTCTGGG | 51317 |
rs760510631 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46000911 | GGCAACAAAAGTGAA[C/T]CTCCGTCTCAAAAAA | 51317 |
rs760511958 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46050591 | TGAAGTAGGTACTTC[C/T]ATAATTTTAATTCAT | 51317 |
rs760600562 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45999457 | TAGTATATACTTCCA[C/T]CAGGTTCTATTCTTT | 51317 |
rs760646572 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46104996 | GAGCAGAAAACTAAG[C/T]TTCAGTACCATTTAT | 51317 |
rs760686806 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45944719 | TTCACCACTCTTCAT[A/G]AACATCAGCCTCCTG | 51317 |
rs760687723 | snp | C/T | 4.71698e-05 | 0.0048562 | intron-variant | PHF21A | GRCh38.p7 | 11:45965632 | GAAAGAGAGAATAAT[C/T]ATTGTATTACTTAAG | 51317 |
rs760710794 | in-del | -/AG | | | intron-variant | PHF21A | GRCh38.p7 | 11:46079872 | AGGAAAGGAAAGGAA[-/AG]AGGAAAGGAAAGGAA | 51317 |
rs760712574 | snp | A/C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45962471 | CGAAGTAAGAGAATC[A/C/T]TGAGAATGCAATCTA | 51317 |
rs760763836 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46084681 | ACAACAGAATCATAA[-/TT]TTTTTTTTTTTTTTT | 51317 |
rs760764047 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:45983593 | CAGTAACTGAAAGCC[-/A]GGTGAGCTCTGCAGC | 51317 |
rs760784561 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46026633 | TCTGAATTAGAAAAT[G/T]CAAAAAAAAAATCCT | 51317 |
rs760786916 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46039904 | GTTTAGCTTTCTGCA[A/T]CTTCCCAAGACTTCC | 51317 |
rs760792263 | in-del | -/CAA | | | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46119561 | CTCATCACAACAACT[-/CAA]CTACTTAGAAATCAC | 51317 |
rs760821093 | in-del | -/TAAA | | | intron-variant | PHF21A | GRCh38.p7 | 11:46108586 | ATATATATATATATA[-/TAAA]ATACATATGTAAATG | 51317 |
rs760832047 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45949927 | TCAGAAGAGCACTTC[A/G]CTGTGCTGTTCAGAA | 51317 |
rs760837849 | snp | C/T | 1.6569e-05 | 0.00287824 | intron-variant | PHF21A | GRCh38.p7 | 11:45950285 | AACAAAAGAAGAATA[C/T]GCTTCAGTCTGGGTT | 51317 |
rs760843401 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46041520 | CATCTTGGTTTCAAT[C/T]ATAGCCAGGCCAAAA | 51317 |
rs760848268 | snp | C/T | 3.29679e-05 | 0.00405991 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45935637 | TGAGGTTTACTTACA[C/T]TTATGGAATTGCTGA | 51317 |
rs760849805 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46093317 | TACTCCAATAGTGTC[C/T]CATTGCCTCAGGGAA | 51317 |
rs760874583 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46023233 | TTTAAGTGTAAGCAA[C/T]GGTTTCTTAGCCTTC | 51317 |
rs760874852 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46054682 | ATTCAAATCACTATA[C/G]TCTCACTAATATGCC | 51317 |
rs760891034 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46056127 | TAAAGTAACAAAATA[A/C]CCTTTATGTAATTTA | 51317 |
rs760899712 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46020286 | CAGAGTAAGATCCTA[C/T]GACATGTTTGGGGAC | 51317 |
rs760904586 | snp | C/T | 0.000135079 | 0.00821713 | intron-variant | PHF21A | GRCh38.p7 | 11:45935543 | CAGAAGGACCCGAAA[C/T]AGCCTGGGGCCCACA | 51317 |
rs760937352 | snp | C/T | 0.000144734 | 0.00850563 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45933935 | TGTTCTCCTTGCCGC[C/T]GGGATCCCGTGGCTT | 51317 |
rs760939944 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46108005 | TGTAGGGTATCTTTA[C/T]GCTGATTAAGCAGTA | 51317 |
rs760987950 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46033813 | GTAGGTGGCTGCTAG[A/G]AATCTTTTAATTACA | 51317 |
rs761060978 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45932502 | CTAGAGACACACACA[C/T]GGCAAAATGTCATCG | 51317 |
rs761073999 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46003343 | TGTCTAGTCATCACT[C/T]AGACTCTCTTCGGTG | 51317 |
rs761086135 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46034224 | ATTAGTGCCCCCACC[C/T]CCCCCTTGCATACTT | 51317 |
rs761086862 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45980572 | GCTATTCACAGGTGT[A/G]GTCATAGTGCATGCA | 51317 |
rs761090145 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46073209 | GGCGGGCGCCTGTAG[A/T]CCCAGCTACTTGGGA | 51317 |
rs761123409 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46068655 | CTCAGCTAAGCAATA[G/T]ATGAGCAAAGTGGAA | 51317 |
rs761140254 | snp | C/T | 1.64738e-05 | 0.00286995 | intron-variant | PHF21A | GRCh38.p7 | 11:45979740 | ATCTGCAGCCTGCAA[C/T]GTTCCATCCACACAT | 51317 |
rs761161029 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45961783 | GCCCCATTTTAGAGC[A/G]CTGGAGAGGACAAGG | 51317 |
rs761176797 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45979220 | AATGAAGTTTCACCA[C/T]GTTGGCCAGGCTGGT | 51317 |
rs761192502 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45980817 | AATATGCCATATAAA[C/G]AACACATTCTAAATT | 51317 |
rs761213449 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46083486 | CTTATCCTTCTCTCC[A/G]CTCCCATATCCCCAA | 51317 |
rs761215126 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46067855 | AAGTACCACAATGAG[C/T]GCCAAATAAAGTAGG | 51317 |
rs761230321 | snp | G/T | 1.64817e-05 | 0.00287064 | intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45946042 | AAAGGGAAAAACGGG[G/T]AGGGAAAGAGAGGGG | 51317 |
rs761234769 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46032715 | CTATCTCTTACAAGT[A/G]CACAGACTTGATACC | 51317 |
rs761239339 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46083728 | GAAATTTAAACATCT[G/T]TGAAGATAATCACAT | 51317 |
rs761242486 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46034228 | GTGCCCCCACCCCCC[A/C]CTTGCATACTTTTCC | 51317 |
rs761250900 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45997090 | AAAATTAATAAGACG[C/T]TTAGTATTTCTGAAA | 51317 |
rs761275991 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45974136 | AGCATCTACATACCT[C/G]TTTGTCTAGTATACA | 51317 |
rs761279830 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46098996 | AATTCAAATAAAAGT[C/T]ACTAAGAAAGGTCAA | 51317 |
rs761303006 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46081662 | AACTTTAAGCTGACA[C/T]TGTGTTAACAAAGTT | 51317 |
rs761321132 | snp | A/G | 4.94425e-05 | 0.0049718 | synonymous-codon, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45938219 | TCAGAGGGGGGTCTA[A/G]GCAGTCCAAATGATA | 51317 |
rs761331454 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46099213 | GTAAACCCAACTATA[C/G]CCAGAAGCTTATCCA | 51317 |
rs761353711 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46062628 | GCACATTAGCAGCTT[C/T]CCTTAAATATCTAGT | 51317 |
rs761370712 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45998145 | ATACAAACCATTCTA[C/G]TCGTCTTTGTTTTAA | 51317 |
rs761400036 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46100711 | TGAGATGGAATAATT[A/G]CACCTGTGGGTCTAA | 51317 |
rs761402299 | snp | G/T | 1.64765e-05 | 0.00287019 | missense, utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45979866 | TGCTGCTGTGCTGTT[G/T]GTAGTTTGTTTTCAG | 51317 |
rs761419937 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46046333 | AATATGCAAGGGAAA[C/T]CCACTTCTGGAGGCA | 51317 |
rs761461080 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45997377 | GGACTATACTTCTTA[A/C]AATCCAAATATAAAG | 51317 |
rs761461626 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45941509 | AATGGCAAATGATGG[C/T]TTAGTATCATTATGA | 51317 |
rs761478416 | snp | A/G | 1.86034e-05 | 0.00304982 | synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45965567 | GGGAGGTGGTGCTGG[A/G]GCAATAGGAATGTTA | 51317 |
rs761503250 | in-del | -/TA | | | intron-variant | PHF21A | GRCh38.p7 | 11:46095958 | TTCTCTTCCCCTTAC[-/TA]TATACCAAGCTGATA | 51317 |
rs761517079 | snp | G/T | 1.65627e-05 | 0.00287769 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45965461 | TGACGACACGGACGG[G/T]GTGGATGGAATTCTG | 51317 |
rs761521602 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45942704 | TTCTATGACCCTAGT[C/T]CTCCAAAGGTAACAC | 51317 |
rs761551573 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45979990 | TGAAGACAAAAAGAA[A/T]TAAAAGATATTAGAA | 51317 |
rs761565197 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45936038 | CTCCTAGGACTTTGG[G/T]AGGCCAAGGCAGGTG | 51317 |
rs761565724 | snp | C/G | 1.71091e-05 | 0.00292476 | intron-variant | PHF21A | GRCh38.p7 | 11:45938343 | GAAAGGTAAGAAAAA[C/G]GACAAAAAAGGTAAA | 51317 |
rs761575760 | in-del | -/G | 1.66921e-05 | 0.00288891 | frameshift-variant, utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934055 | GTGGCGGCATTGGCA[-/G]GGGGGGGTGCAGTCC | 51317 |
rs761596730 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46061829 | TTGGTTCACTTTCTC[A/G]TTTGATGGAGAACCT | 51317 |
rs761606805 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46026660 | TCCTTTAAAGTCAAG[C/T]AGTGGAATTAACATA | 51317 |
rs761607908 | snp | A/C | 2.02427e-05 | 0.00318134 | downstream-variant-500B, utr-variant-3-prime, synonymous-codon | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45928867 | GCCGGCGCTGCCCCT[A/C]ATCTTAGCATTGGGC | 51317 |
rs761628740 | in-del | -/A | 1.64966e-05 | 0.00287194 | intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45946058 | GGGAAAGAGAGGGGG[-/A]AAAATGATCTTACAT | 51317 |
rs761642226 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46009929 | AAACAGATAAAGGGG[C/T]CGTCAGTCACTTTAC | 51317 |
rs761651047 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45988351 | GACAGAAAAAGACAA[C/T]AATATTAGAAAAATA | 51317 |
rs761655188 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45937410 | TATAAAATATCGACA[G/T]CACTTTACACTTAGT | 51317 |
rs761657335 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45970951 | AGTGATTTGAGCAGA[C/T]AGCAGAAATGCCATA | 51317 |
rs761684507 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46075219 | CAAATCTATGTTAGT[A/T]CTCACAAACAAAAAT | 51317 |
rs761695242 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46106464 | GGCATCTGTTCCTTT[C/G]AGAAAAAGAATTCTG | 51317 |
rs761704449 | snp | C/T | 8.26754e-05 | 0.00642891 | intron-variant | PHF21A | GRCh38.p7 | 11:46084132 | TTAGCCATTACTTAA[C/T]AACAGTGTGGGAGAA | 51317 |
rs761747345 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45986518 | AAAGTATAAACACAT[A/C]AACTACAATCGAACA | 51317 |
rs761749780 | snp | A/G | 1.69887e-05 | 0.00291446 | intron-variant | PHF21A | GRCh38.p7 | 11:45934244 | CAGCAAATGACAAGG[A/G]CAGTGGCACTGAGCC | 51317 |
rs761772185 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45941580 | ACTCCCAGACTACAC[-/T]TTTGAGAACTGCTGC | 51317 |
rs761802655 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46052428 | GAATTGAGTTTCTAT[C/T]ACTGGAAAGCAGAAG | 51317 |
rs761803546 | snp | A/G | 1.64768e-05 | 0.00287021 | intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45946018 | CCTATATACCAAGAG[A/G]AGGGAACAAAAGGGA | 51317 |
rs761826469 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46063182 | TGAATTGAATTCGCC[-/G]GGGGGGGCTGGCATG | 51317 |
rs761850741 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46094984 | AACTGCTTCCTACTA[C/T]ATGCTAAATTCTATA | 51317 |
rs761858007 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45989950 | TGAGCCATGATCGTG[C/G]CACTGCACTTCAGCC | 51317 |
rs761871600 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45948303 | AATGTCCATGGGAAG[G/T]TCTGAAATATGGGAT | 51317 |
rs761882381 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46079724 | TGAGAACAAGGAAGT[A/G]CAGGAACAATACAAA | 51317 |
rs761890443 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930389 | GGCACACGATGGTGC[C/T]AGCTGGAGGCTGCCA | 51317 |
rs761923398 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45961117 | AAAGTGGAAAAATAA[A/G]TAAAAAGTCCAGTTG | 51317 |
rs761930119 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46028745 | CGCCCAGCTAATTTC[C/T]GTATTTTTAGTAGAG | 51317 |
rs761954165 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46064026 | TCTGTCGATTAACAC[C/G]CTCCCCCAATTTCAC | 51317 |
rs761963993 | snp | A/G | 1.9297e-05 | 0.00310614 | intron-variant | PHF21A | GRCh38.p7 | 11:45935748 | TCTTTTGCTAAAAAA[A/G]AAAAAAAAAAAAAAA | 51317 |
rs761967160 | snp | G/T | 4.77943e-05 | 0.00488824 | intron-variant | PHF21A | GRCh38.p7 | 11:45965635 | AGAGAGAATAATTAT[G/T]GTATTACTTAAGCTG | 51317 |
rs761970057 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46078281 | TACTTCCAAAAATCA[A/G]TGTGCCTCAGTACCA | 51317 |
rs761992892 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46019452 | TGAACCAGGTCCACA[C/T]AGCCCTAAGATGTGG | 51317 |
rs762020114 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46041713 | TTGTAAAATTTCAAA[C/T]ATACATAAAAGTTCA | 51317 |
rs762053708 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45953099 | GGTTGTAACAAAAAC[A/G]CACACTTAACAACTG | 51317 |
rs762054471 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45945231 | GCTCAGTGAGTATCT[C/G]CTGAGTGAATTCTGA | 51317 |
rs762102676 | snp | C/T | | | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934213 | GGATGGTGTTCTTCA[C/T]TTCCATGCATTTCTG | 51317 |
rs762121112 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46003323 | TCTTTTCACACCATC[-/T]TATGTGTCTAGTCAT | 51317 |
rs762128276 | in-del | -/AA | | | intron-variant | PHF21A | GRCh38.p7 | 11:45987069 | TAATTATGAATGCGT[-/AA]AAGAGATGCCCAATT | 51317 |
rs762160490 | snp | C/G/T | 3.29621e-05 | 0.00405958 | synonymous-codon, missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45935654 | TATGGAATTGCTGAG[C/G/T]TGTTTCACCTTTTGC | 51317 |
rs762183820 | snp | A/G | 0.0001882 | 0.00969869 | intron-variant, synonymous-codon | PHF21A | GRCh38.p7 | 11:46049400 | GGCCCAAATACATAC[A/G]TTCAGTAGGTCAAGC | 51317 |
rs762185994 | snp | A/C | 2.26411e-05 | 0.00336453 | intron-variant | PHF21A | GRCh38.p7 | 11:45969918 | TGCTAAAAAATGAGG[A/C]AGATAAATAAACCAG | 51317 |
rs762188169 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46058196 | GAAGGAGAAAGGTTA[A/C]ACTGCTAATATTCTT | 51317 |
rs762201819 | in-del | -/CCAAGGTAATGAAGC | | | intron-variant | PHF21A | GRCh38.p7 | 11:46069572 | CTTACTTATTTGACT[-/CCAAGGTAATGAAGC]CTAAAGGCAATGTAA | 51317 |
rs762221161 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45991312 | GTAGCTAGTGAATTC[C/T]ATAACTGTTACATAA | 51317 |
rs762240874 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45966645 | TTGTTGTTTGAGATG[A/G]AGTCTCGCTCTGTTG | 51317 |
rs762247145 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46022935 | TTTGTATTTTTAGTA[C/G]AGATAGGGTTTCGCC | 51317 |
rs762276758 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46004990 | TCTCTTACTGCAAAT[A/G]TCTCTGAATATGGAA | 51317 |
rs762307222 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45967660 | TCATTGAAGACAAAT[A/G]TCTGATGCTATCTTG | 51317 |
rs762311333 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46108175 | AACCAAGAAGAGAGA[C/T]TACCAGTTTTTTTAA | 51317 |
rs762320973 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45991331 | ACTGTTACATAAAAA[C/T]GAAGTAATAATATCA | 51317 |
rs762322912 | snp | C/G/T | 1.69246e-05 | 0.00290896 | intron-variant | PHF21A | GRCh38.p7 | 11:45953512 | TGAGACCTGCCTTTG[C/G/T]AAACATAGGCCTACC | 51317 |
rs762337114 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45967836 | TTTACTCTGTAATCA[G/T]CATGTGCCTATAGAC | 51317 |
rs762354962 | snp | C/T | 1.66001e-05 | 0.00288094 | intron-variant | PHF21A | GRCh38.p7 | 11:45950295 | GAATATGCTTCAGTC[C/T]GGGTTCTCACAAAGC | 51317 |
rs762368476 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46020335 | AGTGGCTGCTAGTAT[C/G]CTGCAGCAAACCAAT | 51317 |
rs762384328 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46069809 | GTTAAATGTTAAATG[G/T]TCTAAGCTTCTTAGA | 51317 |
rs762387866 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46069955 | ACTCAATGGATACAC[A/G]TGCATTAACTCCTCA | 51317 |
rs762448246 | snp | C/G | | | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46085228 | TGGATATTTTAAAAT[C/G]TATCTATCGTGTGTA | 51317 |
rs762449517 | snp | C/T | 1.80726e-05 | 0.00300599 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45933950 | CGGGATCCCGTGGCT[C/T]CTCCTAGAGGGGCTC | 51317 |
rs762453351 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45952985 | TCTATCCTAAATTAT[A/G]GTATAGATGTTACTA | 51317 |
rs762463305 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46087788 | TGAGATAGGGTCTTA[C/T]TGTGTCACCCAGGCT | 51317 |
rs762490864 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:46120976 | CCTGGCAGCTGGAGG[C/T]AGGAACTCTGAGCAG | 51317 |
rs762525865 | snp | A/T | 3.32298e-05 | 0.004076 | intron-variant | PHF21A | GRCh38.p7 | 11:45950300 | TGCTTCAGTCTGGGT[A/T]CTCACAAAGCCAATT | 51317 |
rs762530779 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45944163 | TGTATATTTTATATA[C/G]TAATATTTTATTAGT | 51317 |
rs762544183 | in-del | -/ACACAC/ACACACAC | | | intron-variant | PHF21A | GRCh38.p7 | 11:46099527 | AGAAAAATTAGACAC[-/ACACAC/ACACACAC]ACACACACACACACA | 51317 |
rs762553284 | snp | C/T | | | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46086090 | AAGGGAGACATACTA[C/T]GGTGAACAAATCTGG | 51317 |
rs762556129 | snp | C/T | 1.64912e-05 | 0.00287147 | intron-variant | PHF21A | GRCh38.p7 | 11:46076747 | CCCCCCTCCCCTTTT[C/T]CCCTACCTGTTTCTC | 51317 |
rs762603086 | in-del | -/ATAGTCATATA | | | intron-variant | PHF21A | GRCh38.p7 | 11:46069513 | TATTAGAGGCTGGAG[-/ATAGTCATATA]TCAGGTAACCAACAC | 51317 |
rs762609466 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45937527 | CTCTTGTCACCCAGG[C/T]TGGAGTGCAGTGGTG | 51317 |
rs762643829 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46101092 | TGGTGGTCCATACAA[C/G]CATCACAGACAGGAA | 51317 |
rs762644355 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46034465 | TCTGGTCTTCTTATC[A/G]TACTAAGGAAGGTCT | 51317 |
rs762655532 | snp | A/G | | | upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46121685 | GGAGGGGGCCGCCGG[A/G]CGGAGTGGTACGGCG | 51317 |
rs762696470 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45998164 | TCTTTGTTTTAAAGA[C/T]TGGTAACTTACTCAC | 51317 |
rs762700198 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46010986 | TTCTCTCTCTCTCTC[A/T]CACACACACACCCCT | 51317 |
rs762727884 | snp | A/C | 1.83118e-05 | 0.00302582 | intron-variant | PHF21A | GRCh38.p7 | 11:45945794 | GATAACGCTTTTCCC[A/C]ATTTAAGCTCTCAGA | 51317 |
rs762728766 | in-del | -/CAC | | | intron-variant | PHF21A | GRCh38.p7 | 11:46040920 | ACACACACACACACA[-/CAC]ACACACACACACGCA | 51317 |
rs762732241 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46047877 | CCATTATTAGGCTGG[C/T]ATTCTTATTGAAAAT | 51317 |
rs762733912 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46099711 | TTATTCCAAATCCAC[A/C]TTTCAAGCACTAAAA | 51317 |
rs762741203 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46115929 | AGTTAATAACACCCT[G/T]AGAGGTTTCATTTTT | 51317 |
rs762747971 | snp | A/G | 0.000122527 | 0.00782613 | intron-variant, utr-variant-5-prime | PHF21A | GRCh38.p7 | 11:46049493 | TAGAGGGAAACAGAT[A/G]GCTTCTAAAAGGGGA | 51317 |
rs762752070 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46063675 | CCACTTTACCCATAA[A/G]GTATATAATTAAGCA | 51317 |
rs762765033 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46012242 | TGTCTTTCCTGACCT[C/T]TTTGTGCAGCTGCAC | 51317 |
rs762782673 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45997487 | CAAAAGATGAAGCCA[A/G]CCCATGCCTACGTGA | 51317 |
rs762788309 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46026802 | GACATTCTGTCCCAC[A/G]TGACTCACCCACTCA | 51317 |
rs762803344 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46116789 | CCAACATGGTGATAC[A/C]CCGTCTCTACTCAAA | 51317 |
rs762811035 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45990865 | AACATTTGTTACAAT[C/T]GAACCTACACTGACA | 51317 |
rs762834030 | snp | A/G | 1.67781e-05 | 0.00289634 | synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45965489 | CTGGGATGTGGGAAG[A/G]GTTGTGGGGGTGAAC | 51317 |
rs762843623 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46093201 | AATTAAAACTTTTCC[C/T]TTAATATTTTAGTAT | 51317 |
rs762847019 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46062719 | CTCATACACTACTGA[A/G]AGGAATGTAAAATAG | 51317 |
rs762849538 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46027602 | TGAAGCAAGCCAATC[A/G]ACGAAATGCACTGCT | 51317 |
rs762864694 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46093789 | CCTATTAGGGCTTTC[-/A]ATGTTAGCTCTTTTA | 51317 |
rs762882144 | in-del | -/AT | | | intron-variant | PHF21A | GRCh38.p7 | 11:45997427 | CTTGCTGCACGTTAC[-/AT]ACTAGAGGATTCAGC | 51317 |
rs762886500 | in-del | -/T | 4.04973e-05 | 0.00449967 | downstream-variant-500B, utr-variant-3-prime, frameshift-variant | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45928869 | CGGCGCTGCCCCTCA[-/T]CTTAGCATTGGGCAG | 51317 |
rs762887659 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45973079 | GTGAGACTTCGTCTC[A/C]AAAAAAAATAAATAA | 51317 |
rs762897439 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45976289 | CTCCTTGACAAGTAC[C/T]TTCTGATCCCTCTAG | 51317 |
rs762968259 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46007274 | AAGCCAGGAATCTGT[A/G]GCACTTTACAGAAGA | 51317 |
rs763028589 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46067018 | GCACCTCATTATTTT[G/T]TAACAGCTACATGTT | 51317 |
rs763048650 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46113671 | TCTCTACTAAAAATA[A/C]AAAAATTAGTTGGGC | 51317 |
rs763075716 | snp | A/G/T | 3.36272e-05 | 0.00410032 | synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45965363 | AGTTTGAGGTCCAGC[A/G/T]AGTCTGGTCCCTGGA | 51317 |
rs763078523 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45932984 | GAACAAAAACAAAAA[-/T]TAAAGAAAGAGAAAA | 51317 |
rs763090637 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45934358 | TGCAGCCCCTGGGCC[G/T]TGCTGTGTTCCTCAG | 51317 |
rs763095635 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45977808 | TTGGTTTTATACAGT[A/C]TTGGTATTGCTTTTT | 51317 |
rs763101503 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45965189 | ATTATCGCACATAAG[C/T]GACAGCTTACTGACA | 51317 |
rs763105823 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45996854 | CCCTAACCACAGTAA[C/T]CTAAAAAAGGTCAAT | 51317 |
rs763117576 | snp | C/T | 1.64822e-05 | 0.00287068 | intron-variant | PHF21A | GRCh38.p7 | 11:45948997 | TAGTGTGGTTATTAC[C/T]AATACTGGCACAAGC | 51317 |
rs763128360 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46079898 | AAGGAAAAGAAAGGA[A/G]AGGAAAGGAAGAAAA | 51317 |
rs763131008 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46016649 | CACATGACATAATCT[A/G]TTTTACACTGCAATT | 51317 |
rs763132806 | snp | A/G | 1.73887e-05 | 0.00294857 | intron-variant | PHF21A | GRCh38.p7 | 11:45971395 | GAAAACAGATATTAG[A/G]ACACTAAATCTAAAC | 51317 |
rs763190181 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46081158 | TAATCAAAAGTCTTT[C/G]TCCCTGATGCTAAGA | 51317 |
rs763191232 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45962537 | CCTCTAAGACTATTA[G/T]GCCAGGCTGCCCAGC | 51317 |
rs763199074 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45938964 | TCAGCCTCCAGAGTA[G/T]CTGGGACCACAGGCA | 51317 |
rs763227003 | snp | A/G | 1.64754e-05 | 0.00287009 | missense, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45971201 | TGGAGGTTGACTGGT[A/G]TGTTCTGCACATCAG | 51317 |
rs763251091 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46102851 | GTTTTGATAATAGCT[C/T]AGTATCTCCCTGTTT | 51317 |
rs763277279 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46074632 | CTCAGCCTCCCAAGT[-/A]GCTGGGACTACTGGC | 51317 |
rs763315176 | snp | G/T | 1.65633e-05 | 0.00287774 | synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45953587 | GATGGTGCGGCTCTC[G/T]GTTTGTTTCTCATCT | 51317 |
rs763340232 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46043894 | TGGATGTGAGTGCAG[A/C]AAACAGTAAAAGATG | 51317 |
rs763360904 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46007486 | GTCCAGCTTATTTTT[C/G]TATTTTTAGTAGAGA | 51317 |
rs763390612 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45951448 | TTTATATTATTTCTT[A/C]TTTCAAAAACTGAGA | 51317 |
rs763407053 | snp | A/T | 2.3747e-05 | 0.00344572 | intron-variant | PHF21A | GRCh38.p7 | 11:45935764 | AAAAAAAAAAAAAAA[A/T]GGAACGGTTTTTGAC | 51317 |
rs763417460 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46100030 | CTTTGAAATGTCAAT[A/G]AGAAGTGGAAACAGC | 51317 |
rs763422411 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46002799 | GTTTTATCTTTATTC[A/C]AAAGACCCTTCTTCC | 51317 |
rs763427142 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45992995 | CAGAAAACTGAAAAC[C/T]ACCTTGCTGAAGCTA | 51317 |
rs763432411 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46042596 | CTTATGACTAGGACA[C/T]GGTGCTAGATCTGAA | 51317 |
rs763442151 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46006333 | AAATTCTTAATCTTT[C/T]GGTTGTATATACAAT | 51317 |
rs763447365 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45953411 | GAATAATAAAAGTGC[A/G]TAAGAAAATGAACAT | 51317 |
rs763448478 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46023857 | GCTACTCAGGAGGCT[A/G]AGGCAGGAAAATTGC | 51317 |
rs763461381 | in-del | -/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45967078 | TTATGATAAAAATGA[-/C]CCTTTCCTGGCCGGG | 51317 |
rs763487639 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46111813 | TAAAGAATTAAGATT[C/T]TTTGAAACTACACTT | 51317 |
rs763514252 | in-del | -/TG | | | intron-variant | PHF21A | GRCh38.p7 | 11:45979354 | CTTTCTATCTGGTCC[-/TG]CAAGAGCACTGATCC | 51317 |
rs763539107 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45968868 | CCTGGTGGGTGGAGA[C/T]TGCAGTGAGCCTAGA | 51317 |
rs763548993 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46018948 | ATCAATGTATCATAC[C/T]GTAAGCAGCAAGAAC | 51317 |
rs763565588 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46016199 | ACCATCATATATGTG[A/G]TCTGTTGTTGACCTA | 51317 |
rs763580840 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45933745 | AACCTCCAGCTGGCA[C/G]TATTTCATGTAACAT | 51317 |
rs763600694 | in-del | -/AACATGACAAAACCCCGTCTCTACT | | | intron-variant | PHF21A | GRCh38.p7 | 11:45968743 | GAGACATTCCTGACC[-/AACATGACAAAACCCCGTCTCTACT]AAAAATACAAAAATT | 51317 |
rs763603680 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46110290 | AACTTCCCAAGAGTG[C/T]ACAGCTACGTGACAG | 51317 |
rs763614385 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45994328 | TTTATCTTACTGCCA[C/T]AAAAATTATGTAGCT | 51317 |
rs763621548 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46038735 | AAGCATGCTAGCATA[C/G]TTGCTCAGGTTTCTC | 51317 |
rs763638669 | snp | C/T | 1.72276e-05 | 0.00293487 | downstream-variant-500B, stop-gained, synonymous-codon, utr-variant-3-prime | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45928825 | GCCCTGCAGCAGCCC[C/T]AGAGCCCTGCCCGAG | 51317 |
rs763643908 | snp | C/T | 1.64743e-05 | 0.00287 | intron-variant | PHF21A | GRCh38.p7 | 11:45979743 | TGCAGCCTGCAATGT[C/T]CCATCCACACATTTA | 51317 |
rs763648897 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45941461 | CAATATCTGGTAAAC[C/G]CCACTGTTCGGTCTT | 51317 |
rs763659808 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46031765 | GAAAAGAATGCAATA[A/C]TTTTTTTCCAGAGAC | 51317 |
rs763681087 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46044368 | GGGTCAGCTGACCTA[C/T]TCAAATCTATAGTGA | 51317 |
rs763688711 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46005068 | CTAATACAGCAGTCC[C/T]CCACATCAGTAATTT | 51317 |
rs763697760 | snp | A/G | | | upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46122225 | TGAAGGGGGGGGGGG[A/G]AAGCCGTGAGGGGCA | 51317 |
rs763702708 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45957130 | AACAGAGCCCCAAAA[C/T]ATATGAAGAAACTAT | 51317 |
rs763725156 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46097854 | ACATACACAAAAGAA[C/T]AGAATACCTTGTACA | 51317 |
rs763756378 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46060282 | AGATTACAGGCATAA[A/G]CCACTACACCCCAAC | 51317 |
rs763761687 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46073199 | CAGGCGTGGTGGCGG[C/G]CGCCTGTAGTCCCAG | 51317 |
rs763782838 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46035877 | AAATTTGCGAGCCAC[A/G]TTAAGATTTTGGACT | 51317 |
rs763789737 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46117650 | TATTTGTATTAATAT[C/T]ATAGGGATGATAACA | 51317 |
rs763804794 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45953088 | TGTAATACAATGGTT[G/T]TAACAAAAACGCACA | 51317 |
rs763853870 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46090157 | TTGAAAATGGAGGAG[A/G]TTGGGGAGTAAGGTA | 51317 |
rs763907329 | snp | A/G | 1.64876e-05 | 0.00287116 | synonymous-codon, missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934133 | GGAGAGGTCGATGCC[A/G]TGGATGAGGCGAATC | 51317 |
rs763985455 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46001072 | AGTAATGCTACAGCA[A/C]TAGCTCAACATATCT | 51317 |
rs763989266 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45984933 | CTTTTATTCCTTCCA[A/T]GAATCAACATGCAAT | 51317 |
rs763991894 | snp | A/G | 0.000237913 | 0.0109041 | synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45965348 | CTTGCTAAGCTGTAC[A/G]GTTTGAGGTCCAGCG | 51317 |
rs764003224 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45973036 | TGAGCCGAGATCACA[A/C]CATTGCACTCCAGCC | 51317 |
rs764009363 | in-del | -/AAAG | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PHF21A | GRCh38.p7 | 11:45932986 | ACAAAAACAAAAATT[-/AAAG]AAAGAGAAAAGAAAC | 51317 |
rs764015682 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45959949 | AAAAGATGCTCAGCA[C/T]CATTAGTCATTAGGG | 51317 |
rs764047102 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46037334 | TCTTCTAGCCTTCAG[A/G]CCTATTGATAAAAAA | 51317 |
rs764048353 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46062976 | GAGACGACCAAGAAC[A/G]CTTCAGAGGTGATGC | 51317 |
rs764094089 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46088394 | CTGATATCTAATGGC[C/T]TCTAACTTTCCAATA | 51317 |
rs764099034 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46039851 | CCTAAGATTAAAAAT[A/G]TCTGCATGAATGAAA | 51317 |
rs764101290 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46048074 | AGTTGCACAACTCCA[C/G]AATTAATTCCAGAAC | 51317 |
rs764105516 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45974515 | CTAGAGTGCAGTGGC[A/G]TAATCACAGCTCACT | 51317 |
rs764120309 | snp | C/G/T | 6.49039e-05 | 0.00569635 | intron-variant | PHF21A | GRCh38.p7 | 11:45969914 | AACCTGCTAAAAAAT[C/G/T]AGGAAGATAAATAAA | 51317 |
rs764162797 | in-del | -/ATTATA | | | intron-variant | PHF21A | GRCh38.p7 | 11:46014004 | ATTTCTTTGAAAAAC[-/ATTATA]ATTATATTTATTTAT | 51317 |
rs764170278 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46035870 | ATCACACAAATTTGC[A/G]AGCCACGTTAAGATT | 51317 |
rs764177573 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46041612 | AAGGTACAGGTCCTA[C/T]CCAATTTGTTGCTTT | 51317 |
rs764201763 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46078109 | TCCAATTTAAATTGT[A/G]ACTATACCAAAAAAA | 51317 |
rs764212038 | in-del | -/TATGAGT | | | intron-variant | PHF21A | GRCh38.p7 | 11:45941060 | CCCAGAGAGCTTTTA[-/TATGAGT]TATATCTATTAATAT | 51317 |
rs764225815 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46117236 | TATCAAACTTTCTAG[A/C]ATCCCCAAATTTTTA | 51317 |
rs764251737 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46026972 | GCTTTTGCTAGCATT[C/G]TCCATTTTTATGTAG | 51317 |
rs764277205 | snp | A/G | 1.68227e-05 | 0.00290018 | missense, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45945859 | GTGGAGGTGGGGCTG[A/G]GCAGGGACACAGGCT | 51317 |
rs764285885 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45999575 | TGAGAAGGGAAATTT[A/G]AAAATATATCTATAG | 51317 |
rs764302743 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46093320 | TCCAATAGTGTCTCA[C/T]TGCCTCAGGGAATAT | 51317 |
rs764328123 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930738 | GCCCAGTGGGCAGCC[A/G]CTCCAGCTCTCTGAA | 51317 |
rs764345327 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45949871 | TGTAACTGTTGTCAA[C/T]ATTCTGATAACCTGG | 51317 |
rs764364203 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45962617 | AGAACATTGGCCAGG[C/T]GTGGTGGCTCATGCC | 51317 |
rs764380998 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45991183 | TAATAAGCATGTAAG[C/G]TTCTTCTATGTTTTT | 51317 |
rs764390461 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46108006 | GTAGGGTATCTTTAC[A/G]CTGATTAAGCAGTAC | 51317 |
rs764394973 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46092034 | CTACGTGAAATTAGA[C/T]AATTCATTTCCACTT | 51317 |
rs764398471 | snp | A/G | 1.90911e-05 | 0.00308953 | intron-variant | PHF21A | GRCh38.p7 | 11:45935550 | ACCCGAAACAGCCTG[A/G]GGCCCACACGTACTG | 51317 |
rs764400309 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45948588 | CTTTTACATGGGGTT[C/T]TGTTCACTGTGCTAT | 51317 |
rs764420297 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46040315 | GGAAGGAAATACCTG[C/T]ACTACAGTGATGACA | 51317 |
rs764433616 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46069514 | ATTAGAGGCTGGAGA[C/T]AGTCATATATCAGGT | 51317 |
rs764460167 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46067450 | GGCCCCAGACTCATT[C/T]ACTAGTTTATACAAC | 51317 |
rs764468772 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46004823 | CCTCCTGAAAATACC[A/G]TCTCTCCCTCTCTCC | 51317 |
rs764469990 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46018926 | ATGCAAGACTTTTTA[G/T]GACAAAATCAATGTA | 51317 |
rs764478304 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45966580 | AACCTGAGGTAACAT[A/G]CCTGATTTTTAATAG | 51317 |
rs764486568 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46107025 | CTGTCCCCACGGCTG[C/T]CTCTTCTGCAGGAAG | 51317 |
rs764508240 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46054690 | CACTATACTCTCACT[A/C]ATATGCCACTAGAAG | 51317 |
rs764567003 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46003468 | AATATTCATAGTACT[A/G]ATGACACTAAAACAA | 51317 |
rs764582150 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45982549 | AATTAAACTGCTGTA[A/G]TTTAGGAGAAGGCAA | 51317 |
rs764584691 | snp | G/T | 4.94442e-05 | 0.00497188 | missense, utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45979863 | GGTTGCTGCTGTGCT[G/T]TTTGTAGTTTGTTTT | 51317 |
rs764600709 | snp | C/T | 1.64803e-05 | 0.00287052 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45979868 | CTGCTGTGCTGTTTG[C/T]AGTTTGTTTTCAGAT | 51317 |
rs764601160 | snp | A/G | 4.94173e-05 | 0.00497053 | synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45948914 | CCCAGGGTGCATTGT[A/G]CTGTTTAGGTATGTC | 51317 |
rs764633290 | snp | G/T | | | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46085364 | AGATAATGTCAAAAG[G/T]CTAAATCTGTTAATA | 51317 |
rs764636534 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46068666 | AATAGATGAGCAAAG[C/T]GGAAAAAAAAAATAC | 51317 |
rs764663741 | in-del | -/A | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45932678 | TTAAGTAACACTAGG[-/A]AGACCTCAATATCTT | 51317 |
rs764686399 | in-del | -/AT | | | intron-variant | PHF21A | GRCh38.p7 | 11:46026063 | TGCCAAGTTATCTAA[-/AT]ATATCCTGGTATCAG | 51317 |
rs764726611 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46067860 | CCACAATGAGCGCCA[A/G]ATAAAGTAGGCACAA | 51317 |
rs764730185 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45979320 | TACTGAGCCCAGCCA[C/T]AGCACCCTTCCAAAT | 51317 |
rs764736732 | in-del | -/TAAACTAAATAA | 1.77491e-05 | 0.00297896 | intron-variant | PHF21A | GRCh38.p7 | 11:45971406 | TTAGGACACTAAATC[-/TAAACTAAATAA]TAAACTAAATCCCAC | 51317 |
rs764739930 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45966652 | TTGAGATGGAGTCTC[A/G]CTCTGTTGCCAGGCT | 51317 |
rs764755191 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:45982337 | GCCAATTTTGGGGGG[-/A]AAAATTCTGCTATGC | 51317 |
rs764766209 | snp | G/T | 1.65869e-05 | 0.00287979 | intron-variant | PHF21A | GRCh38.p7 | 11:45950162 | TTTCAGGAACAAAGC[G/T]GTGGGCCAGAAAAAA | 51317 |
rs764769862 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45979362 | TCTGGTCCCAAGAGC[A/T]CTGATCCTGGAATAG | 51317 |
rs764771772 | snp | A/G | 1.64738e-05 | 0.00286995 | intron-variant | PHF21A | GRCh38.p7 | 11:45938352 | GAAAAAGGACAAAAA[A/G]GGTAAAATTTTAATG | 51317 |
rs764798357 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46081983 | CATTCCATATGGAGT[A/G]AATACCCTGAAAATT | 51317 |
rs764827710 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45980883 | CTGGGACAGGTTCTG[C/T]GGCGGTACACACGTT | 51317 |
rs764827793 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45992477 | CCCAGGAGGCAGAGC[C/T]TGCAGTGAGCTGAGA | 51317 |
rs764839102 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:45944096 | TGAAGCAGGAAAAAC[-/A]AAAGTGTCACAAAAG | 51317 |
rs764839850 | snp | C/T | 0.000186237 | 0.009648 | intron-variant, utr-variant-5-prime | PHF21A | GRCh38.p7 | 11:46049436 | CTAGCTTCAACACAG[C/T]GTATTCCTGTACAGT | 51317 |
rs764849967 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45942731 | ACACTTTCTTTGTTA[C/T]CTCTGGAATTTTAAC | 51317 |
rs764859496 | snp | C/G | 1.80873e-05 | 0.00300721 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45933938 | TCTCCTTGCCGCCGG[C/G]ATCCCGTGGCTTCTC | 51317 |
rs764872886 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46099306 | AGTCCTTGCTTTAAA[A/C]ACAGAAGAAAACTCC | 51317 |
rs764881991 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45957595 | GAGAGAAATGAAAAC[A/G]AGGCCACAACATACC | 51317 |
rs764882805 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46047671 | TGTTCTGACAAGAAG[C/G]CAGTGACTAACAACC | 51317 |
rs764913000 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46061834 | TCACTTTCTCGTTTG[A/T]TGGAGAACCTCCTCC | 51317 |
rs764913623 | snp | C/T | 2.03668e-05 | 0.00319108 | downstream-variant-500B, utr-variant-3-prime, missense | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45928869 | CGGCGCTGCCCCTCA[C/T]CTTAGCATTGGGCAG | 51317 |
rs764983188 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46067256 | AGACAGGTAAAAACA[A/T]CCCAGGTTGAAGAAA | 51317 |
rs765013089 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45937500 | GTATTATTTTTTTGA[A/G]ACAGAGTCTCGCTCT | 51317 |
rs765013220 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46056365 | GTTTCTATGACAAAG[A/G]TAACTCCAATTATGT | 51317 |
rs765029626 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46052263 | TGCCAGAGGCAACCT[C/T]TGCCAGTACAGGACA | 51317 |
rs765043116 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45996332 | TTATAGAGTGATCTA[C/T]ATTACAATTAGATCA | 51317 |
rs765044358 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46083928 | TTGTTAACACCTTTG[A/G]TATATGAAAAAAATC | 51317 |
rs765045570 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45973002 | GGAATCACTTGAACC[C/T]GTGAGGCAGAGGCTG | 51317 |
rs765072599 | in-del | -/TTGT | | | intron-variant | PHF21A | GRCh38.p7 | 11:46087673 | GGTACATGTTGAATC[-/TTGT]TTGTTTAATTTTATT | 51317 |
rs765110191 | snp | C/T | 4.94319e-05 | 0.00497127 | missense, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45938239 | TCCAAATGATATACA[C/T]GGGAACATGTGTCGC | 51317 |
rs765112356 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45955579 | AGTGCTTTTAAGGAA[A/G]GGCAAATCAATTCCT | 51317 |
rs765125032 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46009974 | ATAAGTATCCTAATT[G/T]GTTCAGCTTCTAACA | 51317 |
rs765125860 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45987946 | CTGTAGCTGCTGTGG[-/T]TTTTCCTCACAAAAG | 51317 |
rs765139800 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45971013 | ATGCTAGAAGAATGA[C/T]GGAAACTGAGAAATC | 51317 |
rs765174841 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45944880 | CCAGGGATTCTCCTG[C/T]CTCAGCCTCCAGAGT | 51317 |
rs765181642 | snp | C/T | | | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46120743 | CCCCTCCCCTCCCCC[C/T]ACCTCCCCCCACAAC | 51317 |
rs765184268 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46075303 | TAAGTTATCTTAACT[G/T]TGCAACAGCATCCCC | 51317 |
rs765229590 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45986644 | AGCACTAAACTATAC[C/T]GCCCTCCTTCCTTCA | 51317 |
rs765236363 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46014255 | CACTTATAAATGAGA[A/G]CATATAATATTCAGT | 51317 |
rs765245779 | in-del | -/AAAAAAAAA | | | intron-variant | PHF21A | GRCh38.p7 | 11:45968934 | GAAACTCCATTGCAA[-/AAAAAAAAA]AAAAAAAAAAAAAAA | 51317 |
rs765259319 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46038459 | TAACTATTTATTGAG[A/C]ACCTCCATGTGCTAC | 51317 |
rs765272011 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46091735 | ATCTTTTTTTAAGAG[A/G]TGAGGGTCTCGTTTT | 51317 |
rs765304227 | snp | A/C/T | 4.94379e-05 | 0.00497161 | intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45946025 | ACCAAGAGAAGGGAA[A/C/T]AAAAGGGAAAAACGG | 51317 |
rs765307583 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45932897 | AAAACAGCTTTTCTA[-/T]TCCTTATTTTAGTTT | 51317 |
rs765312569 | in-del | -/TC | | | intron-variant | PHF21A | GRCh38.p7 | 11:45996828 | ATAGCAGTTTGTGTT[-/TC]TGAGTATATCCCTAA | 51317 |
rs765324306 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46029793 | AAATAACAAATGTCC[A/G]TTAGAGTGCTTTTAG | 51317 |
rs765347957 | snp | A/G | 9.88517e-05 | 0.00702966 | synonymous-codon, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45971194 | AGACGTCTGGAGGTT[A/G]ACTGGTGTGTTCTGC | 51317 |
rs765356087 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46103315 | TAAAGTAAAGAAAAC[G/T]TAATACTATATATTT | 51317 |
rs765382988 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46064501 | GCTTCCTAAACTTGG[G/T]AGTAAATCAACTTTG | 51317 |
rs765406803 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PHF21A | GRCh38.p7 | 11:45933273 | GACTGGGCAGGCTTC[A/G]GGAGTGGTGGGGTTA | 51317 |
rs765407101 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46042507 | AAATCCTAGAAAACC[A/G]AAGAAAGAGATTGGT | 51317 |
rs765413910 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45959304 | TATATGTATATCAAA[C/T]CATCATGTTGTATAC | 51317 |
rs765471348 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46078415 | GATAAACACTCTCCA[G/T]ACTTATGACCTAGTA | 51317 |
rs765502139 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45992573 | TTTTTTGACATCACA[A/T]GGTGAACCAAAAATG | 51317 |
rs765530893 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46025449 | CCTTCCATGATAATC[A/G]ATTAGGTTAGCAGAG | 51317 |
rs765535623 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45991378 | CAGGTAGAACAATGA[C/G]GCTCTGAGTAATTAA | 51317 |
rs765554527 | snp | A/G | 2.37285e-05 | 0.00344437 | intron-variant | PHF21A | GRCh38.p7 | 11:45969925 | AAATGAGGAAGATAA[A/G]TAAACCAGAGAGAAC | 51317 |
rs765559540 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46077082 | TTGAGCATCTTGTAC[A/G]GTAAGAGTACCTGTC | 51317 |
rs765564076 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45992710 | AAGTTATATGAATGA[A/G]TTCTGAGAATATGCT | 51317 |
rs765593703 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46042521 | CGAAGAAAGAGATTG[C/G]TGAAATGTATAGCAT | 51317 |
rs765603829 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46042386 | TAGTATGTGTGATAG[-/T]GCAACTCCGGAAAGT | 51317 |
rs765613294 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46094798 | TCAGCTACTCGGGAG[C/G]CTGTGACAGGAGAAT | 51317 |
rs765620164 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46005040 | ATTTTAACACATGCA[C/T]GTATACACCCAACTA | 51317 |
rs765628940 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45951357 | TCAGCCTATTTGAAA[A/C]TAAACTTCTTCAGCA | 51317 |
rs765644243 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46006198 | AATGATTTTAAAATT[A/C]AATGTTATAAACTTC | 51317 |
rs765646721 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45967666 | AAGACAAATGTCTGA[A/T]GCTATCTTGCTCACA | 51317 |
rs765653256 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46093446 | TTCATGCAGTTAGCA[C/T]TCATTTCCAAAGAAA | 51317 |
rs765655766 | in-del | -/CCTGCAG | | | intron-variant | PHF21A | GRCh38.p7 | 11:46058102 | AGGATCTCACTTAAA[-/CCTGCAG]AAAACAGAAACTAGA | 51317 |
rs765697829 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46069841 | AAGTAGTACTTTACA[C/G]GTAAGATGAAAGTGT | 51317 |
rs765699221 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46109697 | TCAAGAATTTGTCTA[C/T]TGGGCCAGGCGTGGT | 51317 |
rs765709203 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:45957595 | GAGAGAAATGAAAAC[-/A]AGGCCACAACATACC | 51317 |
rs765718880 | snp | A/G | 9.24531e-05 | 0.00679838 | intron-variant | PHF21A | GRCh38.p7 | 11:45935560 | GCCTGGGGCCCACAC[A/G]TACTGTTACGTATAT | 51317 |
rs765720602 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45950106 | AATCATACTCTATTT[C/G]TGTTCCAATTTTCTA | 51317 |
rs765744826 | snp | C/T | 3.32817e-05 | 0.00407919 | intron-variant | PHF21A | GRCh38.p7 | 11:45950301 | GCTTCAGTCTGGGTT[C/T]TCACAAAGCCAATTG | 51317 |
rs765760692 | snp | G/T | 1.66164e-05 | 0.00288235 | intron-variant | PHF21A | GRCh38.p7 | 11:45950297 | ATATGCTTCAGTCTG[G/T]GTTCTCACAAAGCCA | 51317 |
rs765768321 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46056904 | CAAGCACAAACAGTG[C/G]GCTGAGGTACTTTTT | 51317 |
rs765769421 | in-del | -/AAG | | | intron-variant | PHF21A | GRCh38.p7 | 11:46101528 | TTTTTAAATTTCCAT[-/AAG]AAGAAGTTATTTAAA | 51317 |
rs765775594 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46071814 | CAATTATGCTAATAT[A/T]TAAAGCTGTTAAAAA | 51317 |
rs765784597 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46040429 | CTTAGCAATCTAATT[A/G]TAAGTAGAAGAGAAA | 51317 |
rs765834713 | snp | C/T | 3.29652e-05 | 0.00405974 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45935682 | TGCTCTAGTTGTTCT[C/T]GTTCTTGTTTTAAAT | 51317 |
rs765851369 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45943562 | TCCCTATAGGCCCTT[C/T]TCTTCTGCATATTTT | 51317 |
rs765856510 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45951460 | CTTATTTCAAAAACT[C/G]AGATGGGCACCTATC | 51317 |
rs765856907 | in-del | -/GCACCTATG | 1.67147e-05 | 0.00289086 | intron-variant | PHF21A | GRCh38.p7 | 11:45935594 | AAGGCCTAGGTCTCT[-/GCACCTATG]GCACCTATGTATCGA | 51317 |
rs765874631 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46005110 | GGCTCAGTTACCAAG[A/G]GCAACCGCAGTCCAA | 51317 |
rs765887601 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46057177 | ACTGGGTCATGTCCA[A/G]TGGGCTAGTAATGCT | 51317 |
rs765896594 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46047326 | TGGAGTTGAAAACAT[C/G]AAAGAAAGGGAAAAA | 51317 |
rs765902113 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45937593 | TCAAGCGATTCTCCT[G/T]CCTCAGCTTCCCAAG | 51317 |
rs765913676 | snp | A/G | 1.66665e-05 | 0.00288669 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934043 | GGCCGGCGTGGAGGT[A/G]GCGGCATTGGCAGGG | 51317 |
rs765925340 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45969049 | ATATCATCTTATCTC[A/C]TATTAGCACTGCCCA | 51317 |
rs765929008 | snp | C/T | 1.64876e-05 | 0.00287116 | intron-variant | PHF21A | GRCh38.p7 | 11:46076750 | CCCTCCCCTTTTCCC[C/T]TACCTGTTTCTCACT | 51317 |
rs765935005 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46064017 | ATTTCAAGTTCTGTC[A/G]ATTAACACCCTCCCC | 51317 |
rs765942584 | in-del | -/AT | | | intron-variant | PHF21A | GRCh38.p7 | 11:45969921 | TAAAAAATGAGGAAG[-/AT]AAATAAACCAGAGAG | 51317 |
rs765942961 | snp | C/T | 6.63801e-05 | 0.0057607 | synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45953593 | GCGGCTCTCTGTTTG[C/T]TTCTCATCTGTTTCT | 51317 |
rs765975725 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46069992 | AATCCAAACATTCCA[C/T]GAATATGGAAAGAGA | 51317 |
rs765985715 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46034618 | AGCAGACAAAAATTA[C/T]GGTGACTATCCAGCT | 51317 |
rs766006304 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46035578 | GATAAAATATAATGA[A/G]TGTTAGGATAAAGGG | 51317 |
rs766008277 | snp | A/C | 0.000100338 | 0.00708229 | synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45965486 | ATTCTGGGATGTGGG[A/C]AGGGTTGTGGGGGTG | 51317 |
rs766011459 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45998178 | ATTGGTAACTTACTC[A/C]CAGCTAGGTTTCCAT | 51317 |
rs766018076 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45967911 | TGTGCTATGTACTCT[C/T]AATAGTTCATATTCT | 51317 |
rs766035359 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46109714 | GGCCAGGCGTGGTGG[-/T]TTTAGGCCTGTAATC | 51317 |
rs766080929 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45977608 | ACCCAATTCTGTTTA[A/C]AACTTAAACAAAAAT | 51317 |
rs766104389 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46012410 | TTGTTTCCTCCCTAT[A/C]GTCATTCCCTGGATA | 51317 |
rs766109708 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45943050 | TGATGGCTCTTCAAA[A/G]TATATGCAGACGTGA | 51317 |
rs766116013 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46083940 | TTGGTATATGAAAAA[A/T]ATCTTTTCAGTTCTT | 51317 |
rs766124618 | snp | C/T | 0.000189807 | 0.00974 | intron-variant | PHF21A | GRCh38.p7 | 11:46049533 | AAACAGAAGGTCAGG[C/T]AGAAGAGGGTGTGGC | 51317 |
rs766143791 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45965668 | CAAGTCCTATAAAAG[A/C]AAATCTTCCACACTC | 51317 |
rs766173265 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46081414 | TCTTGATTTTCCTTT[C/T]TGATTTGGTTACCAG | 51317 |
rs766174517 | in-del | -/ATC | | | intron-variant | PHF21A | GRCh38.p7 | 11:45943098 | TGCTTCTTCCAAGCT[-/ATC]ATCATCATCATCTTT | 51317 |
rs766191435 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46048601 | ATGGTGAAACCCCAT[C/G]TCTACTAAAAATACA | 51317 |
rs766199078 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45981050 | ATGTAAGCCCCATGA[A/G]TGCAGGGGCTTATTT | 51317 |
rs766199908 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45941678 | GCAGAGGAAGTCCTA[C/T]GGAGGCACCATACCA | 51317 |
rs766199955 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45959653 | CTCAAAGAATCCATA[A/G]AACAAATACTAGAGC | 51317 |
rs766209867 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46116599 | TGAGAAACTGACTAG[A/G]CAGCATTTTTTCAAA | 51317 |
rs766265509 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46113899 | AGATGTATTTTATAA[A/G]TAATTTTTCTTGAAG | 51317 |
rs766278292 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930962 | ACAGGGAGATTGGGT[A/G]CCAGGGGCCTCTTCT | 51317 |
rs766286175 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45957871 | AAGAATAACAAAATC[A/G]ACAAACCTCTGGCTT | 51317 |
rs766288066 | snp | C/G | 2.25813e-05 | 0.00336008 | intron-variant | PHF21A | GRCh38.p7 | 11:45965623 | CCTATAGGGGAAAGA[C/G]AGAATAATTATTGTA | 51317 |
rs766303940 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46011280 | GATCACCTGAGGTCA[A/G]GAGTTCAAGGCCAAT | 51317 |
rs766328194 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46115973 | AGTGTTTTTCTCACC[A/G]TTCACAGAAGCAAGT | 51317 |
rs766351823 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46037471 | ACATGGAGAAACCCC[A/G]TCTCTACTAAAAATA | 51317 |
rs766362418 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46062755 | TCACTTTGGAAAACA[G/T]TTTGGCAGTTTCTTA | 51317 |
rs766371382 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46076428 | ACACGCAGCACCTAC[A/G]AGATTCTCTATCACC | 51317 |
rs766378508 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46001498 | CCAGTTGGTGTCTCC[A/G]TCACATGCACCACAG | 51317 |
rs766382508 | in-del | -/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45932628 | ATAGCACTTTTGTAA[-/T]TTTTTTTTACAATGT | 51317 |
rs766404375 | in-del | -/TG | | | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46085189 | ACAATGCAATATAAC[-/TG]TACTATCCACGAACT | 51317 |
rs766409131 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45965242 | TTGAGAAAATGTATT[C/T]AGAGAAAGCCCAGCA | 51317 |
rs766424492 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45992177 | CACCAGTTTTCAACC[A/C]TCAGACGGTAATTAC | 51317 |
rs766431157 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46052437 | TTCTATCACTGGAAA[A/G]CAGAAGAGTCTTCAC | 51317 |
rs766479863 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45997388 | CTTAAAATCCAAATA[C/T]AAAGGACATCATTTT | 51317 |
rs766480818 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46026649 | CAAAAAAAAAATCCT[G/T]TAAAGTCAAGCAGTG | 51317 |
rs766514920 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45948402 | GATGCCCTCTTCTCA[A/G]AGATTCTAAGTTCTC | 51317 |
rs766579906 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45999809 | TGGGTGAGAAATTCA[C/T]CATGTTTCATTTTGT | 51317 |
rs766580378 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46106547 | CAAGTTACAAAGTTT[A/G]GTCTTCGAGATATGA | 51317 |
rs766586238 | snp | A/G | 1.70313e-05 | 0.00291811 | intron-variant | PHF21A | GRCh38.p7 | 11:45934246 | GCAAATGACAAGGGC[A/G]GTGGCACTGAGCCGC | 51317 |
rs766589406 | in-del | -/CAAC | | | intron-variant | PHF21A | GRCh38.p7 | 11:46011930 | CACAAAAATTAGAAG[-/CAAC]CTGCACACTCTAGGT | 51317 |
rs766594839 | in-del | -/AAATAA | | | intron-variant | PHF21A | GRCh38.p7 | 11:45989684 | AATAAATAAATAAAT[-/AAATAA]AAATAAAAATAAAAA | 51317 |
rs766604906 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45946825 | GTCTGCATTTTATGA[C/G]GGTGGAGACCGGCAA | 51317 |
rs766621759 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46065622 | GCATCTGTACTGATA[A/C]AATTATAACATCTAT | 51317 |
rs766640637 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46093290 | TTAAATATGGTGTTT[A/G]TTGACTGATATTACT | 51317 |
rs766673384 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45976302 | ACTTTCTGATCCCTC[C/T]AGTCAAAATTACTCT | 51317 |
rs766677590 | in-del | -/TACTT | | | intron-variant | PHF21A | GRCh38.p7 | 11:46042031 | GCAATTTTCCTACTA[-/TACTT]AATATGATTTGAGAT | 51317 |
rs766693780 | snp | G/T | 1.64749e-05 | 0.00287005 | missense, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45971208 | TGACTGGTGTGTTCT[G/T]CACATCAGTGCTGAG | 51317 |
rs766696087 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45977809 | TGGTTTTATACAGTA[C/T]TGGTATTGCTTTTTT | 51317 |
rs766711485 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46064539 | TATCTTCTGAAAACA[A/T]AATTTTGCAGGACAG | 51317 |
rs766716655 | snp | C/T | 2.84669e-05 | 0.00377262 | intron-variant | PHF21A | GRCh38.p7 | 11:45969940 | ATAAACCAGAGAGAA[C/T]AATTACTCTTCAATA | 51317 |
rs766722499 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46078866 | GCTATATGACAAGTA[C/T]TAACTCAATATTTTT | 51317 |
rs766755880 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46031376 | AAATGTAGCTCAGAT[C/T]GATTATGTCACTTCC | 51317 |
rs766761246 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45993028 | TAGGGAATTACAGTA[A/G]GCAAAATGTAATAAT | 51317 |
rs766762001 | in-del | -/AAAATACA | | | intron-variant | PHF21A | GRCh38.p7 | 11:46116802 | ACCCCGTCTCTACTC[-/AAAATACA]AAACTTAGCCGGGCG | 51317 |
rs766789598 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45953439 | CATCGAGTTCATTTC[A/G]TCATTCAGAGAGCAG | 51317 |
rs766819387 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46058343 | ACATTGTTGGTAAAA[A/C]GAAACCTGATTAAGA | 51317 |
rs766833436 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46096935 | GTCATTCCCATCTCA[A/G]TAAATGGTAACTCCA | 51317 |
rs766833550 | in-del | -/ACTCTT | | | intron-variant | PHF21A | GRCh38.p7 | 11:46055389 | AAACAAACACAACTC[-/ACTCTT]GATAACTGTTCTACA | 51317 |
rs766845048 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46029959 | AAGACATAATTTGGA[C/T]AGTCTTTATAACTTG | 51317 |
rs766884228 | snp | A/G | 4.6476e-05 | 0.00482035 | intron-variant | PHF21A | GRCh38.p7 | 11:45935765 | AAAAAAAAAAAAAAA[A/G]GAACGGTTTTTGACA | 51317 |
rs766884924 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:45956732 | AGAAAAAAATCAAAC[-/A]AAAAAAGGCAGTATT | 51317 |
rs766892366 | in-del | -/CACACACACG | | | intron-variant | PHF21A | GRCh38.p7 | 11:46040926 | ACACACACACACACA[-/CACACACACG]CACGCACAATTAAGG | 51317 |
rs766934156 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46006346 | TTCGGTTGTATATAC[A/G]ATTAGGGCAAAGGCT | 51317 |
rs766947449 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45951363 | TATTTGAAAATAAAC[-/T]TCTTCAGCAAGCCAC | 51317 |
rs766951685 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46039415 | AAAAAGTCCAAGTCT[C/T]TGTCCCAGGCATAGT | 51317 |
rs766978393 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45958195 | AACATTTAAAGAATT[A/G]GCACCAATCTGTCTC | 51317 |
rs767033768 | snp | A/G | | | intron-variant, missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45935243 | GGCCCACTCGCTCAG[A/G]TGACTAGGAAGAATC | 51317 |
rs767080250 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45954960 | TCTTTGATTTTCTTT[C/T]CTGGCCACTTCCATA | 51317 |
rs767096979 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46112286 | AACAGCCTGAGCTTC[C/T]GATCAAATTATATTG | 51317 |
rs767099715 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46058427 | TGACTAAAAAGGGCA[A/G]GCAGGAACTTAGTCT | 51317 |
rs767128014 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46022860 | AGATCTTGGCTCACT[A/G]CAACCTCCACCTCCT | 51317 |
rs767133317 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46094987 | TGCTTCCTACTATAT[A/G]CTAAATTCTATACAT | 51317 |
rs767150306 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45984645 | ACAGAGAAGGGAGAC[A/G]GAGAGACGGAAGGAC | 51317 |
rs767164480 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45974678 | CAGGCTGGTCTAGAA[C/T]TCGCTCTCACGTAAT | 51317 |
rs767170100 | snp | A/T | | | synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45953608 | TTTCTCATCTGTTTC[A/T]GTGTGAGATTTAACT | 51317 |
rs767189862 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46072026 | AAATATTATACTAAA[C/T]ATTATACTAGGAATA | 51317 |
rs767197410 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46088243 | ATCAGACTCACAAGA[C/T]AGTAACACACTGCAT | 51317 |
rs767200214 | in-del | -/G | 1.66921e-05 | 0.00288891 | frameshift-variant, utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934056 | GTGGCGGCATTGGCA[-/G]GGGGGGTGCAGTCCG | 51317 |
rs767238404 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45999400 | TGGTTGATTATAGGT[C/T]TCTAAACAGATAAAC | 51317 |
rs767258078 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45969275 | TGCTGGAAGAACACT[A/C]TCAGGAGAGTATGGT | 51317 |
rs767262543 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46100614 | TGATAGATGCCAAAT[-/A]AACATCATAACATTA | 51317 |
rs767267964 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46110554 | ATTCCTACAAACCTG[A/G]TATTTTCTATATTGG | 51317 |
rs767276410 | snp | A/G | 5.74399e-05 | 0.00535879 | intron-variant | PHF21A | GRCh38.p7 | 11:45953629 | AGATTTAACTGTCTA[A/G]GAGAGAAAAATTAAA | 51317 |
rs767280918 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45997056 | AGAGATATAAAACTA[C/T]CACAAAATCTTGGTT | 51317 |
rs767330804 | snp | A/G | 1.64942e-05 | 0.00287173 | synonymous-codon, stop-gained, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934127 | AGGTTTGGAGAGGTC[A/G]ATGCCGTGGATGAGG | 51317 |
rs767343267 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45944524 | AAAGCCACAAAGCCC[C/T]GCGCAACTGGCCCAG | 51317 |
rs767344740 | snp | C/T | 1.64773e-05 | 0.00287026 | synonymous-codon, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45945990 | CAGCACTGCATTGTA[C/T]TTTGGAGGACGACCT | 51317 |
rs767351697 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45968033 | ACTAAACCTTAGATT[C/T]CTTACCCTAAAAAGA | 51317 |
rs767357481 | in-del | -/TA | | | intron-variant | PHF21A | GRCh38.p7 | 11:46108571 | GTGTGTGTGTGTATA[-/TA]TATATATATATATAT | 51317 |
rs767366464 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45981119 | GGCCCAACACGGTGG[C/T]TCATGCCTGTAATCC | 51317 |
rs767395445 | snp | C/T | 1.65504e-05 | 0.00287662 | intron-variant, missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:46076825 | AGTCAGCATTCTGAT[C/T]GGAAAGAAAAAATAT | 51317 |
rs767399971 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46027309 | AAACAATATTCCATG[C/T]TAATCTGCCATCGTT | 51317 |
rs767424652 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45939128 | TGAGCCACTGCACCC[A/G]GCCGGGACTACTGTA | 51317 |
rs767433042 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45943283 | GCACACCAGTATGCC[C/T]GGCTAATTTTTGTAT | 51317 |
rs767435299 | snp | C/T | 1.80237e-05 | 0.00300192 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45933966 | CTCCTAGAGGGGCTC[C/T]GTTATTTAGTCTCTT | 51317 |
rs767444383 | in-del | -/TAAC | | | intron-variant | PHF21A | GRCh38.p7 | 11:46096148 | GCCCCAACATCTTAA[-/TAAC]CATCCCTCTTGTACC | 51317 |
rs767505296 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46049641 | ACTCTCCTTGCTGGT[A/T]GCCAGCATGCTCCCT | 51317 |
rs767507866 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46101697 | GAGTGCAGTGGCATG[A/G]CACAATCACAGCCTC | 51317 |
rs767517523 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45933604 | CTCCTCCCTCCGCCC[A/G]TCCCTGCTCCCCACC | 51317 |
rs767537060 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45949890 | CTGATAACCTGGAGT[A/G]ACCAGAAAATATAAA | 51317 |
rs767547750 | in-del | -/AAG | | | intron-variant | PHF21A | GRCh38.p7 | 11:46069038 | ACACAATCACACTCC[-/AAG]AAGACAGGTAAAAAG | 51317 |
rs767570920 | snp | C/T | 1.95781e-05 | 0.00312868 | intron-variant | PHF21A | GRCh38.p7 | 11:45935538 | ATAAACAGAAGGACC[C/T]GAAACAGCCTGGGGC | 51317 |
rs767578057 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46025788 | ATTTGCAAGTCATAG[A/G]CATAATATGGCTTTT | 51317 |
rs767582159 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46039842 | TTAAATTTCCCTAAG[A/G]TTAAAAATATCTGCA | 51317 |
rs767583902 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930506 | GAAGAAATCAAAACC[C/T]CAGAGGAGCTCAGCA | 51317 |
rs767594928 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46048216 | TCTGTCTCCAGGGAG[A/G]TGCATATTCTAAACA | 51317 |
rs767614926 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46055701 | GGAGTCATGGAATCT[C/T]TTTATATAAACGCCC | 51317 |
rs767621246 | snp | A/T | 1.69527e-05 | 0.00291137 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45965500 | GAAGGGTTGTGGGGG[A/T]GAACTTGGTCAGCAT | 51317 |
rs767649073 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46106921 | CCTTCAGCCTTTCAC[A/C]GAAAGAAAGGCTGTT | 51317 |
rs767668078 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46038526 | AGTTGTGTGATTATC[C/T]TTATTAGTTTACTGT | 51317 |
rs767683177 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46075421 | CTTGTCAAACTAACC[C/G]TGAAACTATAAGGAG | 51317 |
rs767700629 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45967490 | ATCCATTGTGGGGAC[C/T]TTGAAGCCATGCCTA | 51317 |
rs767726989 | snp | A/C | 6.59098e-05 | 0.00574026 | intron-variant | PHF21A | GRCh38.p7 | 11:45979723 | CAACAAATCAGTCTA[A/C]AATCTGCAGCCTGCA | 51317 |
rs767732910 | in-del | -/AAAT | | | intron-variant | PHF21A | GRCh38.p7 | 11:46111476 | GCAAGACTCCGTCTC[-/AAAT]AAATAAATAAATAAA | 51317 |
rs767746637 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45987199 | TTCAGTGAGCTATAA[C/T]CATGCCACTACACTC | 51317 |
rs767753642 | snp | A/G | | | upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46122721 | AAGAATTCTTGTTTT[A/G]AGAGATTTCTTGGCG | 51317 |
rs767771311 | snp | A/T | 1.64765e-05 | 0.00287019 | intron-variant | PHF21A | GRCh38.p7 | 11:45949504 | GAAGAAAAGGTTTTC[A/T]TTAGCAGAGAGGCAT | 51317 |
rs767771602 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45948514 | GACAACCAAGACGCT[A/G]TTAGGAACACCTTGG | 51317 |
rs767772530 | snp | A/G | | | downstream-variant-500B | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45929116 | TTGTGTTCCTGGTTT[A/G]GGGGAGCAAGGGCAC | 51317 |
rs767795717 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46090675 | TAATACTTATTTTTT[C/G]TGGAAGTAGAATTCC | 51317 |
rs767803038 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46039235 | TTATCTCCTGTTTTC[A/G]TGCATTCGCTGTTTT | 51317 |
rs767830337 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46065733 | TACTCCTTTTCTTTA[A/C]CAAAAGTTGTTTAAG | 51317 |
rs767842970 | snp | C/G | 1.71717e-05 | 0.00293011 | intron-variant | PHF21A | GRCh38.p7 | 11:45934253 | ACAAGGGCAGTGGCA[C/G]TGAGCCGCCTGGTTT | 51317 |
rs767862784 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930632 | TTACCAGGATGCAGC[A/G]CCTGGACAGGAGCTG | 51317 |
rs767864248 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46031727 | TTTCCTCTGGCTTTG[C/T]CTGTTAGGTCTAATA | 51317 |
rs767909297 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45939054 | AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTGGC | 51317 |
rs767912449 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46001633 | TTTCCCCCATGCTTA[C/G]ATTTTTAAAATTCCA | 51317 |
rs767912518 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46018792 | GTACCAAGAATAACT[A/G]TAGGTAGGAGCAGAT | 51317 |
rs767947366 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45957476 | TAGAAATTAATGACA[A/G]CAGAAAAACTAGAAA | 51317 |
rs767950141 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46043999 | ACAAACTGAGGAAAG[C/G]TTAAGATTGTGGTTA | 51317 |
rs767950387 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46106208 | ATTCTACATTTGTAT[A/C]TGATTTGCTTTTTAT | 51317 |
rs767989452 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45995897 | TCATAATATTCAAAC[C/T]CCAAATTCATTATTA | 51317 |
rs767989689 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45978030 | TGGTGGGCCGGTTGC[A/G]GTGGCTCACACCTGT | 51317 |
rs768002546 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46016762 | ACTACCTGGAGCTTG[A/G]CAGCCCTCAGAAATG | 51317 |
rs768003506 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45959076 | TATGACAAAGCCAGA[C/T]TTATCCCAAGAGTGG | 51317 |
rs768025889 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46099121 | GAAGAAATTAGTGAA[C/T]TGCTAGAGAAAAATA | 51317 |
rs768034063 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46062517 | AGCATCCTCTCCTTG[A/T]TTCACTAATGCAATA | 51317 |
rs768043819 | in-del | -/AT | | | intron-variant | PHF21A | GRCh38.p7 | 11:46115690 | TATGAAAATTCAAAC[-/AT]GTTTCAAGAAATCAG | 51317 |
rs768053596 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46081571 | TTCTATCTGTAAGCA[A/G]TTAAACTGCATTTCA | 51317 |
rs768072903 | snp | C/T | 1.73075e-05 | 0.00294167 | intron-variant | PHF21A | GRCh38.p7 | 11:45969796 | AACCTATCATTGAGC[C/T]TGTCATTGGTTTACT | 51317 |
rs768077632 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45994064 | TGCTGGAGCCAACCC[A/G]ACAAGAATGATATAC | 51317 |
rs768093817 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46040750 | ATGTTCGAATTTAAA[C/T]ACCACTGCAATTTTT | 51317 |
rs768111285 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46030125 | CGCTAAACAATAGAG[A/C]AAACTGCTGACTCTA | 51317 |
rs768123504 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45937753 | CCCAAAGTGCTGAGA[C/T]TACAGGCCTGAGTCA | 51317 |
rs768123939 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46076110 | TTGCCACACTCCACC[C/T]GGTGGCAGGCACTGC | 51317 |
rs768133654 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45988556 | TAATTTAAAAAATCA[C/T]CTACAGTAATAGCAC | 51317 |
rs768143527 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46080220 | CTGGAGTACAGTGGT[A/G]TGATCATGGCTCACT | 51317 |
rs768150140 | in-del | -/AAAAA | | | upstream-variant-2KB | PHF21A, LOC105376661 | GRCh38.p7 | 11:46123378 | AAATTCTGATTTCTT[-/AAAAA]ATAAAATATGGACTT | 51317 |
rs768177079 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45956820 | TAAGTCCCTCCTTAC[C/T]AGTAATCACTTAAAT | 51317 |
rs768180934 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45937354 | CCAAAGAGAGAACGA[-/G]GGAGGCTAGGACAGT | 51317 |
rs768183687 | in-del | -/TAAA | | | intron-variant | PHF21A | GRCh38.p7 | 11:46075854 | TTGTTATTATTTCAC[-/TAAA]TAACATTAAGTAACA | 51317 |
rs768192823 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46116505 | CATCAATGGAGAAAT[A/G]AAGAAAAACTGTAAT | 51317 |
rs768219765 | in-del | -/AGA | | | intron-variant | PHF21A | GRCh38.p7 | 11:46051828 | GGTGGGGAAACATGC[-/AGA]AGAAGAAAAGATAAA | 51317 |
rs768255059 | in-del | -/TA | | | intron-variant | PHF21A | GRCh38.p7 | 11:46064451 | GCTAGGATGAGAGAG[-/TA]GTTAGCCAAACCCTG | 51317 |
rs768265110 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46063085 | AATTATGACTCAATA[A/T]ACCTATAAGAGAGAA | 51317 |
rs768290622 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46027328 | TCTGCCATCGTTTAC[C/T]TTATTTATACATGTA | 51317 |
rs768292837 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46010896 | CAGGCAGTGAACAGC[A/C]TCATACCAGCTCCTT | 51317 |
rs768302997 | snp | A/G | 3.38444e-05 | 0.00411352 | intron-variant | PHF21A | GRCh38.p7 | 11:45938333 | AAGTTGAGAGGAAAG[A/G]TAAGAAAAAGGACAA | 51317 |
rs768343161 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46072382 | CTTGCTCTTTGTTGC[G/T]TCTCCCCCTTCTTAC | 51317 |
rs768344315 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45972554 | AAACCGAGGCAGGTG[C/G]ATCGTCTGAGGTCAG | 51317 |
rs768346889 | snp | A/G | 0.000185649 | 0.00963277 | intron-variant, synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45935208 | TGTGGAAGAAAGAGC[A/G]AGGGAGGGCCGTACG | 51317 |
rs768357642 | in-del | -/ACAC | | | intron-variant | PHF21A | GRCh38.p7 | 11:45955284 | GTCTTTCTCTCTCCA[-/ACAC]ACACACACACACACA | 51317 |
rs768374914 | snp | A/G | | | intron-variant, utr-variant-5-prime | PHF21A | GRCh38.p7 | 11:46075095 | TTAGTTCAGAGAACA[A/G]TTAGAGCTTGCCACT | 51317 |
rs768375908 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45988339 | GTTTTCTTAGAAGAC[A/C]GAAAAAGACAATAAT | 51317 |
rs768376481 | in-del | -/TC | | | intron-variant | PHF21A | GRCh38.p7 | 11:46038117 | GTATACTCCTATTTC[-/TC]TCTCTCTCTCTTTTT | 51317 |
rs768379386 | snp | G/T | 1.67116e-05 | 0.0028906 | utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:46084267 | ATAGTTTCTTCAGCC[G/T]CTGTTTAAAGTAACA | 51317 |
rs768385457 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45948186 | GTACCTTGTTTATGA[G/T]CTCAAACCCTGAGCT | 51317 |
rs768388903 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46018347 | ATGATCTGTTAGCTG[C/T]GCATCATGAAGGTCT | 51317 |
rs768399577 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46039297 | TACTCAGCTTCATTC[C/G]CCACTTTCAATCTGC | 51317 |
rs768416356 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46052352 | CCATGCCTGAAAGCA[C/G]CTATATCCCTGAACT | 51317 |
rs768443735 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46092456 | AGTTTTTCAAGACAA[A/G]CAAAAGTAAGTAGTT | 51317 |
rs768451272 | snp | A/C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46014260 | ATAAATGAGAACATA[A/C/T]AATATTCAGTTTTCT | 51317 |
rs768456465 | snp | A/C/T | 3.29664e-05 | 0.00405984 | intron-variant | PHF21A | GRCh38.p7 | 11:45949519 | ATTAGCAGAGAGGCA[A/C/T]GGAGAACCTAAAAAA | 51317 |
rs768491253 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46054038 | TTCACAAGCAACGTC[A/G]TGGCAGTGGAGGAAG | 51317 |
rs768493678 | in-del | -/AAAATAAAAT | | | intron-variant | PHF21A | GRCh38.p7 | 11:45975323 | TGTCTCAAAGAAAAC[-/AAAATAAAAT]AAAATAAAATAAAAT | 51317 |
rs768501327 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46098050 | ACTGCCTGCCTTACA[A/G]TACTCTATTTCCTTC | 51317 |
rs768539399 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46107527 | ACTGCTACATTCTAC[C/T]AGGTCCAATTCTTAG | 51317 |
rs768553398 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46086631 | TTCTTCTTGAAAACA[A/C]CACTTGGTTTTAATT | 51317 |
rs768580628 | in-del | -/CTG | 4.22003e-05 | 0.0045933 | downstream-variant-500B, cds-indel | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45928914 | TGCCCTCCGCCATCC[-/CTG]CTATTTAAATTATTT | 51317 |
rs768588384 | in-del | -/TGA | | | intron-variant | PHF21A | GRCh38.p7 | 11:46100123 | ATGCCTCAATCACGC[-/TGA]TAAGTAAGTAGTCCT | 51317 |
rs768598732 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46094793 | TAATCTCAGCTACTC[A/G]GGAGGCTGTGACAGG | 51317 |
rs768607195 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46066769 | TATAAAGTTAAACGT[G/T]CTAGCTCTCTTGAAC | 51317 |
rs768631999 | in-del | -/A | 0.000137377 | 0.00828671 | intron-variant | PHF21A | GRCh38.p7 | 11:45938346 | GGTAAGAAAAAGGAC[-/A]AAAAAAGGTAAAATT | 51317 |
rs768646418 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46044474 | CCCCATTTGGATTTC[A/T]TATCTTATTTTCCAA | 51317 |
rs768687273 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46096338 | CTAGTTATTGTCCCC[A/G]TCTAGGCTCACGTTT | 51317 |
rs768687714 | in-del | -/ATATAA | | | intron-variant | PHF21A | GRCh38.p7 | 11:46108583 | TATATATATATATAT[-/ATATAA]AATACATATGTAAAT | 51317 |
rs768688582 | snp | C/T | 1.64822e-05 | 0.00287068 | missense, utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45979792 | TGGGAGAGGCTGCAG[C/T]TGACTGCTGGGCGTG | 51317 |
rs768692641 | snp | A/G | 1.64732e-05 | 0.0028699 | intron-variant | PHF21A | GRCh38.p7 | 11:45948966 | GAGGGTTGAAGGAGG[A/G]AAGGTGACTGTTGAG | 51317 |
rs768693677 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46016448 | TTTCCTGCCTCTGTA[C/T]CTTTGCCTTTGCTTA | 51317 |
rs768708847 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45965041 | GAGGGCAGCAGAGCC[C/T]GTCTGTGAATTTCCA | 51317 |
rs768746508 | snp | C/T | | | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46119178 | TATCCATTATTTATA[C/T]ATAAATGTTCTTCCC | 51317 |
rs768773068 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45953069 | TTGGGGTTTGGGGTT[C/T]TAATGTAATACAATG | 51317 |
rs768776752 | snp | C/T | 3.29451e-05 | 0.00405851 | synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45949432 | TGCTCCACTGTAGAC[C/T]GGATTTGCTGTTGTT | 51317 |
rs768789850 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46042395 | TGATAGTGCAACTCC[A/G]GAAAGTTCATCACCA | 51317 |
rs768790943 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45993729 | ACAGAGTCAGGCTGT[G/T]GAGATCCAAGGAAGT | 51317 |
rs768802457 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45932546 | CTGTGCTAAAAAATT[A/G]TAACTACACGGCATT | 51317 |
rs768816935 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46021768 | GTTGCCCAGGCTGGT[C/G]TTGAACTCCTGGCTT | 51317 |
rs768827249 | snp | A/G | 2.25233e-05 | 0.00335576 | intron-variant | PHF21A | GRCh38.p7 | 11:45935742 | TCTTCTTCTTTTGCT[A/G]AAAAAAAAAAAAAAA | 51317 |
rs768838106 | in-del | -/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46022128 | TATTATAGAACAAAA[-/C]CATGTACTGTTTGTT | 51317 |
rs768842505 | snp | A/G | 8.26016e-05 | 0.00642604 | synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45953569 | GGGTGCAGCAGGTGG[A/G]GTGATGGTGCGGCTC | 51317 |
rs768858158 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46029445 | GTAATCCTAATACAC[-/G]GGGAGGCCAAGGCGG | 51317 |
rs768863033 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45951191 | TAAATATGCCAAATA[A/G]TACATTATCAATTTA | 51317 |
rs768891971 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46023645 | CTTTATCCTCAGTTG[C/T]TAATGTGTGTTAAGA | 51317 |
rs768896671 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46087295 | AGGGTTTAACTTGAA[G/T]ACTGTAAATGTCAAA | 51317 |
rs768898270 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46003135 | AAAACAGGAGTAGAA[-/T]TAATTTCCTCAATAG | 51317 |
rs768910111 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46116377 | TCAGAAAGTTAGCAG[A/G]GTCAGTCAAAACATT | 51317 |
rs768910741 | in-del | -/AG | | | intron-variant | PHF21A | GRCh38.p7 | 11:46082613 | TTAATATGAATAGTA[-/AG]AGAGTGTTTAGAATA | 51317 |
rs768952694 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45967552 | GGGCATAAGGCTTCT[A/T]TGCCAAGGTGGCTTT | 51317 |
rs769010121 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46035134 | TCCCAATATGTCCGC[C/T]CTCTTTTTGGCTTCA | 51317 |
rs769036880 | snp | A/C | 1.65015e-05 | 0.00287237 | intron-variant | PHF21A | GRCh38.p7 | 11:46076736 | TTAAAAATATGCCCC[A/C]CTCCCCTTTTCCCCT | 51317 |
rs769042629 | snp | A/G | 3.31395e-05 | 0.00407046 | intron-variant | PHF21A | GRCh38.p7 | 11:45950286 | ACAAAAGAAGAATAT[A/G]CTTCAGTCTGGGTTC | 51317 |
rs769046406 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46071160 | GTGGCTTCTTTTGGC[C/T]AATGAGATGTTAACA | 51317 |
rs769053462 | snp | A/C | | | missense, stop-gained, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934163 | CAGCTGTTTTACCTT[A/C]TCCAGGGAGCTGTGC | 51317 |
rs769063969 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46105429 | CAGGAAGTAGCACAA[A/C]TGTAAATCTGGTTAA | 51317 |
rs769089921 | snp | G/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45933717 | TATTTCACTTGGCAT[G/T]GTGCTGGCAAAGAAC | 51317 |
rs769098092 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46048852 | TACATATACCTAGGA[A/G]TAACTGCTCAGTCAC | 51317 |
rs769100021 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46034139 | ATCTTTCACATATTT[A/G]CTGTCCACTGATGCT | 51317 |
rs769100422 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45982232 | AAAGTGCTGGGATTA[C/T]AGGCATAAGCCACCA | 51317 |
rs769159524 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45970635 | CGGTTAATTTGTGAG[A/T]TTCTTGAATATTTTT | 51317 |
rs769180986 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46049237 | AAGTAATACAGAACT[C/G]TCAGAGCCAGGCTTT | 51317 |
rs769186489 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45998071 | GAATATACATGTACC[A/T]CTGTGGAGAGAGGCT | 51317 |
rs769199857 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45943778 | ATAGAAACTATCTTA[C/G]GAGATGAAAGTTAAC | 51317 |
rs769208810 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45960419 | TGACTCTCAAAAACA[C/T]GCTAAGTGAAAGCAG | 51317 |
rs769235437 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46100622 | TGCCAAATAACATCA[C/T]AACATTAAAGACACA | 51317 |
rs769258116 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46063221 | AGAAGGAGCTCTTAC[C/T]ATTCTGTATACACCA | 51317 |
rs769264764 | snp | A/G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46063467 | CAAAAGCAGTCAGTC[A/G/T]TAGAGAATATGTAAA | 51317 |
rs769271830 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46102362 | AATTTAAAACCACTA[C/G]GAGAAATCTAAAAAG | 51317 |
rs769278683 | in-del | -/AA | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46119743 | CGAACGTGGTCAGGG[-/AA]GAAAAAAAAAAAAAA | 51317 |
rs769284550 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46072106 | CTAATAAGGAAGACA[A/G]ATATTTAAAAAATAG | 51317 |
rs769291430 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45942474 | CAATACTTCAACTGA[C/G]AAAAAGTTGGGACAA | 51317 |
rs769339237 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45960514 | GAGACAGAAAGCAGA[C/G]TGGTGATTGCCAGCG | 51317 |
rs769351233 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46100779 | CTACCATTACCTTGT[A/G]GTGACTCCTAATGAA | 51317 |
rs769354151 | snp | A/G | 0.000100942 | 0.00710358 | missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934033 | AGGGGGAAGGGGCCG[A/G]CGTGGAGGTGGCGGC | 51317 |
rs769359666 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46118181 | CCATCACTTATACCT[C/T]CTAAAAATACAATTT | 51317 |
rs769424171 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46010173 | CTCTCCTGATATACA[A/C]TCATGAAGCAGTCTC | 51317 |
rs769425506 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930228 | AGGTGGCTGGAGAGG[C/T]AGCCGTGCATGCGGA | 51317 |
rs769431356 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45959220 | ACCCCACTACACACA[A/C]AAAAAAGGTTAACTA | 51317 |
rs769455285 | snp | A/C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45998147 | ACAAACCATTCTAGT[A/C/T]GTCTTTGTTTTAAAG | 51317 |
rs769474102 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46102185 | AACTCCTGAGCTCAA[A/G]TGATACACCAGCCTC | 51317 |
rs769499928 | in-del | -/AC | | | intron-variant | PHF21A | GRCh38.p7 | 11:46040893 | CACTGACAGGAAGAC[-/AC]ACACACACACACACA | 51317 |
rs769503438 | in-del | -/AC | | | intron-variant | PHF21A | GRCh38.p7 | 11:46097828 | CTCCCTAACTAGAAC[-/AC]ACACACACACACATA | 51317 |
rs769505774 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45990757 | TAGAGCAGTTTTAGG[C/T]TCAGAACAAAACTGA | 51317 |
rs769511544 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46062653 | TCTAGTGATTCTTGG[C/T]TATGTTCATATTTAA | 51317 |
rs769542001 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46027408 | GTCCTCAGTATTATA[A/G]TTCTGCACTCAATCG | 51317 |
rs769552290 | snp | A/G | 1.65364e-05 | 0.0028754 | synonymous-codon, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45945948 | ATGACTGGATTGGGG[A/G]GATGTTGGGGTAAGG | 51317 |
rs769572671 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45991947 | AACATGTAAACTGAT[G/T]ATTACATTTTGCAAG | 51317 |
rs769584132 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46040693 | TCCTGAAGCAGCTTA[C/T]ATGAAACTGCATACT | 51317 |
rs769603864 | snp | A/G | 1.95112e-05 | 0.00312334 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45965592 | ATGTTATTCTGGGCC[A/G]CAGGCTTGGGTCGAA | 51317 |
rs769624906 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46107622 | GAGTGTATTCTAGGA[C/T]TAGAAAGGCTTTTTT | 51317 |
rs769663249 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45938768 | CTTAATATTTTCAGA[C/T]TGCAGTTGACTATGC | 51317 |
rs769669377 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46055470 | CATTCAGAATGAGGA[A/G]TGACAATTAAACCAG | 51317 |
rs769684636 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46094528 | ACAAACTACAATAAA[C/T]ACTAGCGAAATATTT | 51317 |
rs769762612 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46054485 | CCTGGGCGCCATTCT[C/T]GAAGATTCTGATTCA | 51317 |
rs769765472 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45950679 | AAGAGAAGGACTGGG[G/T]TCTACATCTTCTTTC | 51317 |
rs769770389 | in-del | -/CAACA | | | intron-variant | PHF21A | GRCh38.p7 | 11:46011852 | TTTATTCTCTCTATG[-/CAACA]CAACAAAACAAAAAG | 51317 |
rs769772586 | in-del | -/AAAAA | 0.0330046 | 0.124149 | intron-variant | PHF21A | GRCh38.p7 | 11:45935742 | TCTTCTTCTTTTGCT[-/AAAAA]AAAAAAAAAAAAAAA | 51317 |
rs769772897 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46069194 | AATATAAGCCAATAG[A/G]ATTTCACCAGGAGAA | 51317 |
rs769782136 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45956307 | TTTAACTTCTCTTTT[C/T]GTTTCCTATATGACT | 51317 |
rs769820274 | snp | A/G | 0.00166898 | 0.0288393 | intron-variant, missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45935227 | GAGGGCCGTACGGAT[A/G]GGCCCACTCGCTCAG | 51317 |
rs769835034 | snp | A/G | 3.29739e-05 | 0.00406028 | synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45950246 | CCCTAGAGACACCAT[A/G]AAGGCAAGTTTCTGT | 51317 |
rs769841386 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46002692 | TTGGACTCTGTCCCC[A/G]TAAAATGTCCTATGT | 51317 |
rs769855518 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45949678 | TCACCTGCAAGACCA[C/T]GCTGTCCTACACGTG | 51317 |
rs769879333 | snp | G/T | 1.85043e-05 | 0.00304168 | downstream-variant-500B, utr-variant-3-prime, missense | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45928847 | CTGCCCGAGGCTGAG[G/T]CTGGGCCGGCGCTGC | 51317 |
rs769888957 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45993821 | TGCTGGGAAACGGGA[C/T]GGTCAGAGATGAGGC | 51317 |
rs769917277 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46030784 | CTTTAAGAAGGTGAC[A/G]ATCATTTCTTCTAAA | 51317 |
rs769922875 | snp | A/G | 1.65941e-05 | 0.00288041 | intron-variant | PHF21A | GRCh38.p7 | 11:45935601 | TAGGTCTCTGCACCT[A/G]TGTATCGACTGCTGA | 51317 |
rs769934758 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45978869 | TTTGCACAGCTACAC[C/T]AAGTTAGAATTTTAT | 51317 |
rs769938535 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46096455 | TGCCTCCCTCCATTC[C/T]TGTGAAGATCACCAA | 51317 |
rs769943846 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45995055 | CTGTACCTAAGCGTC[C/T]TAGAGTCTACTCTGC | 51317 |
rs769968905 | snp | C/T | 1.64833e-05 | 0.00287078 | synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45936564 | TGCTTCTTCCTTCTT[C/T]AGCATCTGAAAAGAT | 51317 |
rs769985624 | snp | A/G | 1.65436e-05 | 0.00287602 | synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45953581 | TGGGGTGATGGTGCG[A/G]CTCTCTGTTTGTTTC | 51317 |
rs770000076 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45970098 | TTTACCCTATAAAAT[A/G]AACCAACCACACTTC | 51317 |
rs770007484 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45954688 | TTTATGAAGCTCTCC[A/G]TAAATACTGAAATAA | 51317 |
rs770021049 | snp | C/T | 3.30038e-05 | 0.00406212 | synonymous-codon, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45971335 | GAGAGGTAGTGTCTT[C/T]GTGGTAATCATAGAA | 51317 |
rs770028867 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45977562 | ATAAACATTTTCTGA[A/T]CAACCTGTACTTTGG | 51317 |
rs770032368 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46111627 | AAGGCACTGCCCTGC[C/T]TCTGCATACATTCAA | 51317 |
rs770039643 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46009043 | GCAGTGGCGTGATCC[C/T]GGCTCACTGCAACCT | 51317 |
rs770053512 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46072564 | CAGAAATTAAGTTTT[C/T]CCTGTTTACATTACT | 51317 |
rs770055107 | snp | C/T | 1.69861e-05 | 0.00291424 | intron-variant | PHF21A | GRCh38.p7 | 11:45938145 | CTCCCCTGTTGGACC[C/T]ACCCACAGTACCTGG | 51317 |
rs770063157 | in-del | -/AAA | | | intron-variant | PHF21A | GRCh38.p7 | 11:45939772 | AGGAGAACATAGCCC[-/AAA]AAAAAAAAAAAAAAA | 51317 |
rs770079017 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45946760 | CTTTAATGATTCTCA[C/G]TTCCCACAAACTGAT | 51317 |
rs770089281 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46043664 | CCACTTTTAGAAGTC[A/G]GCAGCTTTTTCCTTC | 51317 |
rs770093745 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45953196 | ACAGAACACAGTAAT[C/G]ATTAGGAATGTAATG | 51317 |
rs770113422 | in-del | -/TGTGTGCGTGCA | | | intron-variant | PHF21A | GRCh38.p7 | 11:46021523 | CCCTTATTGCACATG[-/TGTGTGCGTGCA]TGTGTGTGTGCATGT | 51317 |
rs770127878 | snp | A/G | 1.69648e-05 | 0.00291241 | intron-variant | PHF21A | GRCh38.p7 | 11:46079114 | TTTAACAATTAAATG[A/G]ATAACAATAGTAGTT | 51317 |
rs770165205 | snp | A/G | 1.88549e-05 | 0.00307036 | intron-variant | PHF21A | GRCh38.p7 | 11:45935756 | TAAAAAAAAAAAAAA[A/G]AAAAAAAAGGAACGG | 51317 |
rs770175280 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45935458 | ACCTACCAACTGGCC[A/G]CCTGTACCTGAGGTC | 51317 |
rs770184273 | snp | C/T | 0.000792511 | 0.0198904 | intron-variant | PHF21A | GRCh38.p7 | 11:46076743 | TATGCCCCCCTCCCC[C/T]TTTCCCCTACCTGTT | 51317 |
rs770191738 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46059350 | CTGAAGAATAATTGA[A/G]AATGTAAAGAAATGC | 51317 |
rs770201916 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45942071 | CAAACATACAGAGAC[C/T]TGTGTGTTGATTTTA | 51317 |
rs770213284 | snp | A/G | 4.03242e-05 | 0.00449004 | intron-variant | PHF21A | GRCh38.p7 | 11:45965300 | GCCCAGAGCAGGTAC[A/G]TACTCTGCCTGTACC | 51317 |
rs770222072 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46054545 | GATTTTTCAAAAGCT[C/T]TTCATTTTATTAGGG | 51317 |
rs770224073 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46018916 | ATGCAATCCAATGCA[A/C]GACTTTTTATGACAA | 51317 |
rs770233815 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45968808 | GGTGGCACATGCATG[G/T]AATCCCCAACTACTT | 51317 |
rs770244959 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46036319 | CCTGAGTCTAAGATG[C/T]CAGTACGACACTGAA | 51317 |
rs770247940 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46083082 | TATTCAACACACCTC[C/T]ATGTTAAACTAATTT | 51317 |
rs770288295 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45964736 | TGTATGTCTCTAGCC[A/T]CGTTTTTTAAGATAA | 51317 |
rs770319558 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45984447 | GCCTCTGACACTTCA[A/G]GTCACAGTTTCCAAG | 51317 |
rs770334972 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46035420 | TCTAGTATGTTTTGA[C/G]TCTGTTGGTTACTTC | 51317 |
rs770354009 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46036665 | TTTCTTGCTTTTCTG[A/C]CTCGACCATTTTTTC | 51317 |
rs770380509 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46000343 | ACTTCTTCATACTCT[A/G]CTGAGAGTTGCAGGA | 51317 |
rs770381162 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46050087 | CAGCAGAGTTAGCGA[C/T]TGCCACTAGGGATTG | 51317 |
rs770409396 | snp | A/C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46104809 | CCAGTGACCAGCACA[A/C/G]TGGTATGCAGCACGT | 51317 |
rs770443412 | snp | A/G | 1.65247e-05 | 0.00287438 | missense, synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934194 | ATCTCCTTCTGCCGG[A/G]CCAGGATGGTGTTCT | 51317 |
rs770468361 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46015741 | ACACAGGGTCACAAT[C/T]ATCAATATTACTGTC | 51317 |
rs770470826 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46102064 | GGTTTCATCATGTTG[A/G]CCAGGATGGTCTCAA | 51317 |
rs770480350 | snp | A/C/G | 9.89299e-05 | 0.00703244 | intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45946056 | GGAGGGAAAGAGAGG[A/C/G]GGAAAATGATCTTAC | 51317 |
rs770491044 | snp | A/G | | | upstream-variant-2KB | PHF21A, LOC105376661 | GRCh38.p7 | 11:46123192 | GTCATTCGCAGAACC[A/G]GAAATAGCCTTGGAC | 51317 |
rs770551672 | snp | A/C | 1.6552e-05 | 0.00287676 | intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45946070 | GGGGAAAATGATCTT[A/C]CATACCTTTGGCCAG | 51317 |
rs770568216 | snp | C/G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45962242 | ATCATCTAAAGGGAA[C/G/T]AGCAGAAAGCAAAAG | 51317 |
rs770571530 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46051888 | ACCAGGAGCCTCTTG[A/C]AATGGTTGGAACAGT | 51317 |
rs770578228 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46102622 | TTAAGTAACATGCCT[A/G]CCTCTTCCTCAACTT | 51317 |
rs770594300 | snp | A/C | 1.65154e-05 | 0.00287358 | missense, utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:46079160 | GCTTCATTTGAGCAA[A/C]CAGTTTCTGGTAATA | 51317 |
rs770596077 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45984529 | GTTCACACGACAGCA[A/T]GACAGATCCTGAAGA | 51317 |
rs770641187 | snp | C/G | | | downstream-variant-500B | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45929127 | GTTTGGGGGAGCAAG[C/G]GCACTCTGGGGCTAG | 51317 |
rs770664720 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46071249 | CTTAGGTAAACTACA[A/G]AATGAATACGCCCCA | 51317 |
rs770666758 | snp | G/T | 3.34459e-05 | 0.00408924 | intron-variant | PHF21A | GRCh38.p7 | 11:45971109 | TGAGGAGCAGCTGCT[G/T]GCTTACCAGAGTGAC | 51317 |
rs770685539 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46014043 | AGATTCAAGGGGTAC[A/G]TGTGCAGGTTTCTTA | 51317 |
rs770704025 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45977237 | TGTTGCCCGGGTTCA[A/G]GTGATTCTCATGCCT | 51317 |
rs770717924 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46077787 | TACATGATCACCAAC[C/T]ATAACAGAAATGATA | 51317 |
rs770729838 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46029373 | TTTTATTCTATATTC[C/T]CTTTGAGTTTAAGGA | 51317 |
rs770747370 | snp | A/G | | | intron-variant, utr-variant-5-prime | PHF21A | GRCh38.p7 | 11:46049437 | TAGCTTCAACACAGT[A/G]TATTCCTGTACAGTG | 51317 |
rs770748050 | snp | C/G | 1.65228e-05 | 0.00287422 | missense, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45945955 | GATTGGGGGGATGTT[C/G]GGGTAAGGGCTCCAA | 51317 |
rs770758953 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45992078 | CAACTGGAGAGGCAG[G/T]GCCCTAATAACACTA | 51317 |
rs770781297 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45952121 | AAATTTTTGATGATA[C/G]AATAAAAAGCTGTCA | 51317 |
rs770796323 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46003592 | GGCAGAGTGAGAAAA[C/T]GCTACAATTCTCACT | 51317 |
rs770807965 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46094614 | CATGAAATCCTGGCC[A/G]TGCACAGTGGCTCAT | 51317 |
rs770811899 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46058021 | TTTTCCGTCAGTTAA[A/G]TTTCCAACCTGGAGA | 51317 |
rs770819420 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46027694 | AGACTAACACACAGA[A/G]CTATGAGAAGACGCC | 51317 |
rs770880517 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46035158 | GGCTTCAGCTAGTTT[A/G]AGCTGAATGTGTAAT | 51317 |
rs770885566 | in-del | -/CAATTCCAGT | | | intron-variant | PHF21A | GRCh38.p7 | 11:45954395 | TCTCCTATTTCGGAA[-/CAATTCCAGT]CATAATCTCAGAGAG | 51317 |
rs770905187 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46041469 | TCAAATGTATATTGG[A/G]AAACTAAGGGGTAAT | 51317 |
rs770994397 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46106509 | GGGTTGGGGGAAGTA[A/C]ACAAATACTAAATAG | 51317 |
rs770995462 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46068458 | TTGGCTCCTAAAAAG[C/T]ATTCGTTATTCACAC | 51317 |
rs771067349 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45940446 | TGATCTGCCCACCTC[A/G]GCCTCCCAAAGTGCT | 51317 |
rs771087186 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46067021 | CCTCATTATTTTTTA[A/C]CAGCTACATGTTATT | 51317 |
rs771093415 | in-del | -/TA | | | intron-variant | PHF21A | GRCh38.p7 | 11:45947131 | GAGACCTGATTTGTG[-/TA]AGAGCATTTTGACTC | 51317 |
rs771094000 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46081344 | ACTGAAACACAAGGT[G/T]TTATACACATACATT | 51317 |
rs771108253 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46045858 | TGCTCATGGTTTACC[C/T]TGAGATGTGGTCACC | 51317 |
rs771117752 | snp | A/C | 1.90242e-05 | 0.00308411 | downstream-variant-500B, utr-variant-3-prime, missense | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45928853 | GAGGCTGAGGCTGGG[A/C]CGGCGCTGCCCCTCA | 51317 |
rs771127315 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46083217 | CTTAAAGAAGCCCAC[A/G]TGCATAGGGCCAACT | 51317 |
rs771127519 | snp | G/T | 3.2981e-05 | 0.00406071 | intron-variant | PHF21A | GRCh38.p7 | 11:45935626 | TGCTGAAGGCATGAG[G/T]TTTACTTACACTTAT | 51317 |
rs771128026 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45996691 | TTTGAAAGTAGGTGT[A/T]GGCACAATTAATCTT | 51317 |
rs771138750 | snp | G/T | 1.65603e-05 | 0.00287747 | intron-variant | PHF21A | GRCh38.p7 | 11:45936606 | TACCTTGAGAAGGAG[G/T]TTTAAACACACATCC | 51317 |
rs771148348 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46033364 | CTGCCTCCTAGGCTC[A/G]AGGGATCCTTCCACC | 51317 |
rs771154244 | snp | G/T | 3.29451e-05 | 0.00405851 | synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45949449 | GATTTGCTGTTGTTC[G/T]TCTTTTTCGCTCTTG | 51317 |
rs771170218 | snp | A/C | 0.000139799 | 0.00835942 | intron-variant | PHF21A | GRCh38.p7 | 11:45971397 | AAACAGATATTAGGA[A/C]ACTAAATCTAAACTA | 51317 |
rs771179559 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46097529 | GAGCAAAAGAATACT[A/C]AAATAAAGACTAAAA | 51317 |
rs771186046 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46061310 | CTGTTTTGATCCCAT[A/G]TGAATCTTAAAATAG | 51317 |
rs771216009 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45995542 | TTGGTGCAGGTAGAG[C/T]GAGATAGAGTGGTTG | 51317 |
rs771217709 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45936976 | TCAATTTTAGATTTC[C/G]ATGTCCCTCAAAGAC | 51317 |
rs771228626 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46109980 | GCAAGACTCCGTGTC[-/A]AAAAAAAAAAAAAAA | 51317 |
rs771240060 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46032347 | TTTATATAACAATCT[A/G]GGATCATACACTGCA | 51317 |
rs771261232 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46010204 | TGGGCATTTCTAAAG[-/A]AAAATTAATAATGGA | 51317 |
rs771261872 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46046474 | CAAGAAACCAGAGCT[C/T]GTCATACAGGGCAAG | 51317 |
rs771263963 | snp | C/T | 1.65444e-05 | 0.00287609 | synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45965417 | CTGGGCCATGGGGAA[C/T]GTTTTGGCTATGGTT | 51317 |
rs771265757 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:45963422 | TAAAACTCTGTGTCA[-/A]AAAAAAAAAAAAAAA | 51317 |
rs771282720 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45939007 | CCCGACTAATTTTTT[A/G]TATTTTTAGTAGAGA | 51317 |
rs771286788 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45964496 | CAGAAGATTCAGGAT[C/T]ACCACAGACTATTTT | 51317 |
rs771310265 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46009191 | GATAGCCAGGCTGAT[C/T]TCCAACTCCCGACCT | 51317 |
rs771313972 | in-del | -/CACCTGCCAC | | | intron-variant | PHF21A | GRCh38.p7 | 11:45938978 | AGCTGGGACCACAGG[-/CACCTGCCAC]CACCCCCGACTAATT | 51317 |
rs771353839 | snp | A/G | 1.6898e-05 | 0.00290667 | intron-variant | PHF21A | GRCh38.p7 | 11:45938152 | GTTGGACCCACCCAC[A/G]GTACCTGGTCCTGAC | 51317 |
rs771358428 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46082371 | ACCCCTACCTTGATG[C/T]CATTTCTGGCATGCC | 51317 |
rs771402560 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46023935 | CACTCCATCCTGGGC[A/G]ACACGGCAAGACACC | 51317 |
rs771403384 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46115093 | TGCCTTCAACTGAGA[C/T]ATTTTCACCAAAGTC | 51317 |
rs771410575 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45996038 | AACCTCAAACTCCCC[A/G]GCTCAAGTGATCCTC | 51317 |
rs771417826 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46043912 | ACAGTAAAAGATGGA[A/T]CGCAGCAACTGCTTT | 51317 |
rs771437440 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46113953 | CCCATATTCTAATAT[C/T]GCCCACCAGGAAATA | 51317 |
rs771442018 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46024897 | TTCTATACCATAGTG[A/C]CTCCTAGTTCTAGAC | 51317 |
rs771446500 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46079968 | GCTGCCCAAAGTTAA[C/T]AATAACCATAGACAG | 51317 |
rs771469180 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45971967 | GCATGTCGCCTCTGA[G/T]GTAGTTACCCTGGAG | 51317 |
rs771491417 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46113622 | ATTACGAGATCAAGA[A/G]ATCGAGACCATCCTG | 51317 |
rs771498407 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46025157 | ATATGTTGAAAGAAA[A/C]TAATTTTCTCTGGGG | 51317 |
rs771527707 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46038182 | CTCAGGCTGGAGTGC[A/G]GTGGCACAATCTCAG | 51317 |
rs771552967 | snp | C/T | 1.65192e-05 | 0.00287391 | utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:46084221 | GTCTGCAACTCCATC[C/T]TCTACCTTCTCCACT | 51317 |
rs771556381 | snp | A/G | 1.65781e-05 | 0.00287902 | utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:46084243 | TTCTCCACTTTCTCT[A/G]CTAATTCTATAGTTT | 51317 |
rs771558979 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45970345 | TGGTTGAGTGACCTC[A/G]TTGCTTCTCTAAGGA | 51317 |
rs771560407 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46066120 | AAATAAGCCAGACAG[-/A]AAAAAAGTAGGCTCT | 51317 |
rs771565539 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46074792 | ACAGGCGTGAGCCAC[C/T]GTGCCTGGCCAATAA | 51317 |
rs771603970 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46112390 | CTAATTCTAAACGTT[G/T]ACTGAGCCCTTATTA | 51317 |
rs771651902 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46106092 | ATTGCAGCTCCCTCC[A/G]TTGACATCGTAAAGT | 51317 |
rs771653282 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46072942 | AAGTGCTTTGGCTCC[A/G]TATCAGAATATCTCC | 51317 |
rs771680389 | in-del | -/AAG | | | intron-variant | PHF21A | GRCh38.p7 | 11:46079652 | CCACTGTCTTCTCTC[-/AAG]AAGGAGTTCGGTGCA | 51317 |
rs771682088 | snp | G/T | 1.66726e-05 | 0.00288722 | missense, synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934215 | ATGGTGTTCTTCATT[G/T]CCATGCATTTCTGCA | 51317 |
rs771700814 | snp | G/T | 1.64833e-05 | 0.00287078 | missense, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45971312 | GTCGCAGTTGCTGCT[G/T]TCAAGACGAGAGGTA | 51317 |
rs771701056 | in-del | -/ATAAAA | | | intron-variant | PHF21A | GRCh38.p7 | 11:46108585 | TATATATATATATAT[-/ATAAAA]TACATATGTAAATGC | 51317 |
rs771717351 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45946337 | TTTCTAGTGCAAGAA[C/G]CAAGATGTCAAAGCC | 51317 |
rs771724553 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46039092 | AAGGATGGGTTGTGG[A/G]GTCTGACAGACAACT | 51317 |
rs771740815 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45970836 | CATAAATGAAACAGT[A/G]TGTATGCCTCTGTGA | 51317 |
rs771762693 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45947656 | CCAAGGTCTTTCTGG[A/C]TCATTTAACCCCTGT | 51317 |
rs771768027 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46041764 | TAAATCAGATACCTA[C/T]ATACCCTTCCACGCT | 51317 |
rs771768590 | in-del | -/T | 4.97896e-05 | 0.00498922 | intron-variant | PHF21A | GRCh38.p7 | 11:46079091 | TTTTATTTTAAATTA[-/T]TTTTAAATTTAACAA | 51317 |
rs771769835 | snp | C/T | 0.000185684 | 0.00963366 | intron-variant, synonymous-codon, utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45935149 | CTCTAGAAAGCCCGC[C/T]TCCTCACACTGGTCA | 51317 |
rs771785246 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46089939 | CCTTCACAAGTCTGT[A/G]TAGTGTCCTGGACCC | 51317 |
rs771803328 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45962347 | CTTCCATGGCTACAT[A/G]CATTACATTGTTTTA | 51317 |
rs771806973 | in-del | -/AGCAAC | 1.64743e-05 | 0.00287 | intron-variant | PHF21A | GRCh38.p7 | 11:45948846 | CACACACAAAGCAAA[-/AGCAAC]AGCAACAGCAGCAAG | 51317 |
rs771824053 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46000834 | CTGAGGCAGGAGGAT[C/T]GCTTGAACCCAGGAG | 51317 |
rs771836226 | snp | A/G | 1.75888e-05 | 0.00296548 | intron-variant | PHF21A | GRCh38.p7 | 11:45946104 | TCCTCATTGGCTAGC[A/G]TGGAAAAGGAAGTGA | 51317 |
rs771852591 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45964762 | GATAAAATCTGACTT[C/T]AGGAAATATAAATGA | 51317 |
rs771862291 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46030614 | TGAACACAAAATTCA[A/G]AAAGATTCTTTAATC | 51317 |
rs771910736 | in-del | -/CT | | | intron-variant | PHF21A | GRCh38.p7 | 11:46007229 | TGAGAAAAGGGCCCC[-/CT]GTCTTTTCAAGGAAT | 51317 |
rs771921762 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46079546 | CCCCACACAAAACCG[A/G]CCTGTTCATACACAG | 51317 |
rs771982973 | snp | A/C | 1.656e-05 | 0.00287745 | intron-variant | PHF21A | GRCh38.p7 | 11:45950282 | AGAAACAAAAGAAGA[A/C]TATGCTTCAGTCTGG | 51317 |
rs772021138 | in-del | -/AAC | | | intron-variant | PHF21A | GRCh38.p7 | 11:46065732 | TTACTCCTTTTCTTT[-/AAC]AAAAGTTGTTTAAGC | 51317 |
rs772024741 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46101618 | GAAATGCCTGGTATA[G/T]ATCTTAGAAGCTACT | 51317 |
rs772034560 | snp | G/T | 1.65124e-05 | 0.00287331 | missense, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45971150 | GCCACAATTTGGACA[G/T]CCTCTGCCCCAGGCC | 51317 |
rs772037178 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45978571 | TTCTCTCTATATAAA[A/G]ACACAGTGAAGACCT | 51317 |
rs772058135 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46029496 | AGTTCAAGACCAGCC[A/T]GGGCAACATGGTGAA | 51317 |
rs772068162 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46017852 | TAGCCACCCAAATTG[C/T]TCTTATTACTTTGCC | 51317 |
rs772068987 | snp | C/T | 6.60186e-05 | 0.00574499 | intron-variant | PHF21A | GRCh38.p7 | 11:45935614 | CTATGTATCGACTGC[C/T]GAAGGCATGAGGTTT | 51317 |
rs772074298 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46058780 | TTATTACATTCTCTT[C/T]ACAAAATCTGGAACA | 51317 |
rs772122372 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45990972 | ATATAATGACATACA[A/G]CCACCATTATACTAT | 51317 |
rs772126934 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45977455 | TTTGATTTTTATAAC[A/G]TAAAATGTTACTTGA | 51317 |
rs772133757 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46018250 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 51317 |
rs772144840 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45950968 | TCAATCACACATGAA[C/T]CTAAAAATTATGGAG | 51317 |
rs772145492 | snp | A/T | | | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46118926 | TGTAAACAAATATCA[A/T]AAACACTGAAAAGTA | 51317 |
rs772152315 | in-del | -/CACACACACACACACG | | | intron-variant | PHF21A | GRCh38.p7 | 11:46040920 | ACACACACACACACA[-/CACACACACACACACG]CACGCACAATTAAGG | 51317 |
rs772160635 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46090179 | AGTAAGGTATGAGAG[C/T]ATAGTGACAATGAGG | 51317 |
rs772173184 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45966487 | CTCACTAAAAACAGT[C/G]AAAAAAAGTTACAGT | 51317 |
rs772173645 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46093238 | ATTTAAACTCCACTA[C/T]ATGCTATGCTCTAAA | 51317 |
rs772189942 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46055771 | CATTTATAAGTTACA[C/T]AGCAGGGGATTCATT | 51317 |
rs772200573 | in-del | -/GTGTGTGTGC | | | intron-variant | PHF21A | GRCh38.p7 | 11:46030811 | TAAACCACATAGTGT[-/GTGTGTGTGC]GTGTGTGTGCGTGTG | 51317 |
rs772205797 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46068530 | AGTCCCTAAACATTC[C/T]GAAATACAGATATGT | 51317 |
rs772212782 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46005748 | ATAATATTTGTAGCA[A/C]AATTAAGCTTCCATA | 51317 |
rs772216470 | snp | C/T | 3.31345e-05 | 0.00407016 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45953543 | TGAGGGTTCTCCTCC[C/T]GTTTTGGTTTGGGTG | 51317 |
rs772244666 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46033547 | GGGATTACAGGTGTG[A/C]GCCACCATGCTTAGC | 51317 |
rs772267768 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46069401 | TTTCCATCACAATGA[C/G]AAGATTTCTAAGACA | 51317 |
rs772268825 | snp | G/T | 1.65444e-05 | 0.00287609 | intron-variant | PHF21A | GRCh38.p7 | 11:45979987 | AAATGAAGACAAAAA[G/T]AAATAAAAGATATTA | 51317 |
rs772302834 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46004773 | GACTAAAGGACTCAT[C/G]ATCTAAAAGATGTCT | 51317 |
rs772315953 | in-del | -/TTG | | | intron-variant | PHF21A | GRCh38.p7 | 11:46083913 | AGATTTCTTTCTTTT[-/TTG]TTAACACCTTTGGTA | 51317 |
rs772324325 | in-del | -/AC | | | intron-variant | PHF21A | GRCh38.p7 | 11:45991558 | CTGCAGTAAGCTTAT[-/AC]ACACACACACACATG | 51317 |
rs772356797 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45997844 | AACCTCCCTCACCAG[C/T]AATAGGTCCTCTTAT | 51317 |
rs772392027 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46019898 | AAAGCCCATATGCTT[A/T]ACTTTCAGGGTTCCT | 51317 |
rs772448272 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45997064 | AAAACTATCACAAAA[C/T]CTTGGTTTTGAAAAT | 51317 |
rs772466588 | snp | G/T | 1.64852e-05 | 0.00287094 | missense, utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45979816 | GGGCGTGGTGGTGGT[G/T]GTACTGCTGCTGTTG | 51317 |
rs772488190 | snp | A/G | 0.000138615 | 0.00832395 | downstream-variant-500B, utr-variant-3-prime, missense | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45928907 | GGCAACCTGCCCTCC[A/G]CCATCCCTGCTATTT | 51317 |
rs772499684 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46111164 | TTTGCTATATAAACA[A/G]GTACTTTAAAAAATA | 51317 |
rs772509051 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45932361 | CCCTGATACCATCCA[C/T]GCTTCCATTTGGGCT | 51317 |
rs772515299 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46026294 | TTTGTAGTAAAATGT[A/G]CCTTAGGGGGAAACT | 51317 |
rs772521775 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46009374 | CTACCTTTGAGGGTT[A/C]TGACACATTCCATTT | 51317 |
rs772526475 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45942004 | CTAGAAATGCCTGCC[C/T]CTCAAGTGTTATTGT | 51317 |
rs772532230 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46100380 | TTATAAATAACGTTA[A/G]CTATTTGCTATTTCC | 51317 |
rs772566668 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46098657 | AAATCACTCCTTATC[C/T]CAAGACAACTCAAAC | 51317 |
rs772583830 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46046217 | AGTGAATAGCAGCAG[C/G]AGAAATCCAGGTCCA | 51317 |
rs772600228 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46010695 | CCAGCGTGCAAAGCC[C/T]TGACCCACAGAAGTT | 51317 |
rs772602190 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46028942 | ATGCCCCAAAGGACT[A/G]TATGAACACAAGTTG | 51317 |
rs772614999 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46061378 | AATAGGAATAGCATT[G/T]AATCTGTAAATTGCT | 51317 |
rs772615464 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930277 | ACACGGTCACCCTCA[C/G]GGAAACAGCTGTGTG | 51317 |
rs772620179 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46098866 | AGGAGGAGGATCAAC[A/G]CCCAGCACTGCATCT | 51317 |
rs772643050 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46115311 | TAAGACTGAATTGAG[A/G]GACAAGTAATAGAAA | 51317 |
rs772685816 | snp | C/T | 1.80543e-05 | 0.00300447 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45965545 | TAAGCTGAGGAGCTG[C/T]GAGCATGGGAGGTGG | 51317 |
rs772700844 | snp | A/G | | | missense, utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45979888 | TGTTTTCAGATTGTG[A/G]CAATGGCTGTATTTG | 51317 |
rs772704707 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46026539 | AAGCTTTAGCTACCT[C/T]TTCTCTACCCTGTTC | 51317 |
rs772707430 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45942925 | TCCCTCCTCAGATCT[G/T]CTCCTCTCTTAATCT | 51317 |
rs772716619 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46069907 | CCAACAATTTCCTTT[C/T]AAACAGAACTCACCT | 51317 |
rs772717160 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46014473 | TGTGGCAATGAACAT[A/G]CAAGTGCAAGTGTAC | 51317 |
rs772733580 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46102436 | AAGATCAATATATAA[C/T]AAGGCATCAGTGGTA | 51317 |
rs772740423 | snp | A/G | 3.30573e-05 | 0.00406541 | missense, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45945952 | CTGGATTGGGGGGAT[A/G]TTGGGGTAAGGGCTC | 51317 |
rs772742543 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46047685 | GGCAGTGACTAACAA[C/T]CAGAAAGCCTGAGAT | 51317 |
rs772754445 | in-del | -/A | 2.03813e-05 | 0.00319222 | intron-variant | PHF21A | GRCh38.p7 | 11:45969907 | TTGCCTGAACCTGCT[-/A]AAAAATGAGGAAGAT | 51317 |
rs772773440 | snp | C/T | 1.67049e-05 | 0.00289002 | intron-variant | PHF21A | GRCh38.p7 | 11:45938322 | ATCACCCTATAAAGT[C/T]GAGAGGAAAGGTAAG | 51317 |
rs772775116 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46012219 | CCCTCAGAAAGTATT[A/C]AAATCTTTGTCTTTC | 51317 |
rs772802768 | snp | A/T | | | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46085695 | CAATAAGATTCATGA[A/T]CTTCATATTTCTAAA | 51317 |
rs772821474 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46100952 | AAGTGAAACAAGCAT[C/T]CCTTAACCAATACAC | 51317 |
rs772841107 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45999203 | TGTAAACAGAGAAGA[A/G]AGCAGTAAATAGAGA | 51317 |
rs772845561 | snp | C/T | 1.64931e-05 | 0.00287163 | intron-variant | PHF21A | GRCh38.p7 | 11:46076744 | ATGCCCCCCTCCCCT[C/T]TTCCCCTACCTGTTT | 51317 |
rs772907449 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46116733 | CTTTGGGAGGCCAAG[C/G]CAGGTGGATCACCTG | 51317 |
rs772957304 | snp | C/T | 1.99209e-05 | 0.00315596 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45965598 | TTCTGGGCCACAGGC[C/T]TGGGTCGAACCTATA | 51317 |
rs772992239 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45973912 | TCAATGTACTTTTGT[C/T]TCAAGTAAATCATCA | 51317 |
rs773034566 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46010961 | CTCCTCTGTATAAAA[A/T]ACTTTCTCTTTCTCT | 51317 |
rs773045696 | snp | A/G | 1.67897e-05 | 0.00289733 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45969835 | GAAGAAAGTTTGGAC[A/G]TGGAGTGAGTCTAGG | 51317 |
rs773059672 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46041159 | CTCTTTCCCCATAGC[C/T]CACCACCACAGTTTC | 51317 |
rs773103093 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46077708 | CAATGAGATCACCCA[C/T]ACCTGTTGTCCAACA | 51317 |
rs773105061 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46062710 | GCTAGAACTCTCATA[C/T]ACTACTGAAAGGAAT | 51317 |
rs773121416 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46034866 | CTGGCCACACAAATC[A/C]AAGTACTTCCTCAAG | 51317 |
rs773122851 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46026798 | ATGCGACATTCTGTC[A/C]CACATGACTCACCCA | 51317 |
rs773126783 | in-del | -/A | 1.65111e-05 | 0.0028732 | intron-variant | PHF21A | GRCh38.p7 | 11:46079174 | CCAGTTTCTGGTAAT[-/A]AAAGAGAGAAAAAGA | 51317 |
rs773140239 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46016544 | AGATCAAACACCATT[C/T]CTTACATAAACCCTT | 51317 |
rs773144122 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46032430 | CCATGTGAAAATCAG[G/T]ATCATCTACTTCCTT | 51317 |
rs773145495 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46039773 | GGATCTCAGTCAAAA[C/G]TGCACAATCTGCAGC | 51317 |
rs773149369 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45990804 | CCACATACTCCTGGC[C/T]TCCCCACCCCACATC | 51317 |
rs773176413 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45983290 | GCAAACTTACATCAG[C/T]CCTTGAGAGGAGGGA | 51317 |
rs773193373 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46076413 | GACAGGTAACAAGGT[A/G]CACGCAGCACCTACA | 51317 |
rs773196416 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46093162 | TTTAGGTTTTGGGAT[C/T]CCAATCCAATATTAG | 51317 |
rs773209259 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46068856 | AACTCAGCAAACTGA[G/T]GCATCTGGTACAAGT | 51317 |
rs773230662 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46030840 | GTGTGCGTGTGTGTG[C/T]GTGTGTGTGTGTGTG | 51317 |
rs773234242 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46066367 | TTTATCTGTATGGTA[G/T]ACCTCAACAGTTTTT | 51317 |
rs773243359 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46004442 | GAGACACTGGGGAGT[A/G]GGGAAGGGGTAGAGG | 51317 |
rs773255017 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45995147 | TTCAGGTTGGCTGCT[A/C]AGGCAAGTGTGATAG | 51317 |
rs773291494 | snp | C/T | 3.31664e-05 | 0.00407211 | intron-variant | PHF21A | GRCh38.p7 | 11:45935602 | AGGTCTCTGCACCTA[C/T]GTATCGACTGCTGAA | 51317 |
rs773332364 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46065472 | TGACCAGAATGAATA[C/T]GGGTCCTGATAGTGT | 51317 |
rs773342340 | in-del | -/AGGAA | | | intron-variant | PHF21A | GRCh38.p7 | 11:46079852 | GAAAGGAAAGGAAAG[-/AGGAA]AGGAAAGGAAAGGAA | 51317 |
rs773345019 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45949681 | CCTGCAAGACCACGC[C/T]GTCCTACACGTGGTT | 51317 |
rs773348693 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46058963 | AGATGAAGAGACACA[A/G]GAGACAGAGACTCCA | 51317 |
rs773349314 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:45971906 | TTTTTTTTTTTTTTA[-/A]TGGTGTCACCCTGGA | 51317 |
rs773364702 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46090942 | ATTTGCAACCTCTGG[C/T]ATAAATGGGTTAAGG | 51317 |
rs773390106 | snp | A/G | 1.72409e-05 | 0.00293601 | intron-variant | PHF21A | GRCh38.p7 | 11:45971388 | AGACAGGGAAAACAG[A/G]TATTAGGACACTAAA | 51317 |
rs773420254 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46079890 | GGAAAGGAAAGGAAA[A/C]GAAAGGAAAGGAAAG | 51317 |
rs773431870 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45977749 | AATTTATGTAGGCTG[C/T]CCTAGCTATCTGATT | 51317 |
rs773450851 | in-del | -/AT | | | intron-variant | PHF21A | GRCh38.p7 | 11:46092028 | GTATAGCTACGTGAA[-/AT]TAGACAATTCATTTC | 51317 |
rs773461665 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45953305 | TTTTCCTTTGATACA[A/G]TCAAAATGCCTATGT | 51317 |
rs773463801 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45995045 | AATTGTCAGACTGTA[C/T]CTAAGCGTCCTAGAG | 51317 |
rs773482080 | snp | A/G | 1.64792e-05 | 0.00287042 | intron-variant | PHF21A | GRCh38.p7 | 11:45948992 | TTGAGTAGTGTGGTT[A/G]TTACTAATACTGGCA | 51317 |
rs773493010 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46029874 | AACAAAGGCATAGAA[C/G]AAGATAAGAATGTGA | 51317 |
rs773515169 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46076261 | ACCGAAGTTTTTTCA[C/T]GTAATAGTAGGTCAA | 51317 |
rs773524052 | snp | A/G | 1.65471e-05 | 0.00287633 | intron-variant | PHF21A | GRCh38.p7 | 11:45935757 | AAAAAAAAAAAAAAA[A/G]AAAAAAAGGAACGGT | 51317 |
rs773541231 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45935519 | GCCCAAGTTAATCAC[A/G]TTAATAAACAGAAGG | 51317 |
rs773546299 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45954692 | TGAAGCTCTCCGTAA[A/G]TACTGAAATAATTTT | 51317 |
rs773558284 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46096620 | TCTTTCCCAACTCTC[C/T]GGCTACTCTCTTTGG | 51317 |
rs773560230 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46110177 | ATAAAGTACATTCAT[A/G]AGTATTATCTTATCT | 51317 |
rs773564577 | in-del | -/AT | | | intron-variant | PHF21A | GRCh38.p7 | 11:45991572 | TACACACACACACAC[-/AT]GCACGCGTGCACTTT | 51317 |
rs773578855 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46059556 | TCAGCTTCCCAAGTA[A/G]CTGGGACTACACACA | 51317 |
rs773582616 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46071381 | TGAAGCAGAGGTGCC[G/T]GGCCAAGTACAGCCT | 51317 |
rs773590062 | snp | A/C | 1.64762e-05 | 0.00287016 | missense, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45971195 | GACGTCTGGAGGTTG[A/C]CTGGTGTGTTCTGCA | 51317 |
rs773612103 | snp | G/T | 1.64969e-05 | 0.00287196 | intron-variant | PHF21A | GRCh38.p7 | 11:45936577 | TTCAGCATCTGAAAA[G/T]ATTTTTAGAATTTTA | 51317 |
rs773613191 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46036449 | TCTGTCAAATTCCCC[A/G]AAATATTCACTGGAA | 51317 |
rs773755465 | in-del | -/AC | | | intron-variant | PHF21A | GRCh38.p7 | 11:45955286 | CTTTCTCTCTCCAAC[-/AC]ACACACACACACACA | 51317 |
rs773755538 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46058220 | TATTCTTAGATGTCA[A/G]GTATTATAACCTCAC | 51317 |
rs773773637 | in-del | -/GGAAA | | | intron-variant | PHF21A | GRCh38.p7 | 11:46079831 | GAAGCCCAAACAAAT[-/GGAAA]GGAAAGGAAAGGAAA | 51317 |
rs773788697 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46055142 | GAGAACTTAAGATAC[-/T]TTGAAGCAATCTGAA | 51317 |
rs773798520 | in-del | -/TATT | | | intron-variant | PHF21A | GRCh38.p7 | 11:46108123 | GCCCCAATTCTTGCC[-/TATT]TACTTTGTAAATGTG | 51317 |
rs773812465 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46072824 | CCGAAGCTGCAACCA[C/T]GATGGCTTAACCCTG | 51317 |
rs773855356 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46041392 | ACTTCTTTCGAGCAA[C/T]AACATTTTTTGTTGC | 51317 |
rs773888687 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46106353 | AACTCTCTAACAGCA[A/G]TAATTACAATATGTT | 51317 |
rs773891104 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46035630 | CAACCAACAGGTGGA[A/C]CTAACCTAATCTATA | 51317 |
rs773893667 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46023986 | AAAAGAATCACTGAA[G/T]GGCATAGAGCATGTA | 51317 |
rs773900885 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45984506 | ACATTCAGCGATACT[A/C]TCAACGTGTTCACAC | 51317 |
rs773913744 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45999300 | CAAGGAAACTTTTTT[C/G]AGATTAAAAATAAAA | 51317 |
rs773959586 | in-del | -/TATA | | | intron-variant | PHF21A | GRCh38.p7 | 11:45956672 | CACTAAGAAAATAAT[-/TATA]TATATACAGAAACAG | 51317 |
rs773962478 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46102805 | GAGGGCCCAAAGTAG[A/G]GGGTATCCCCACAAA | 51317 |
rs773965504 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45946171 | GAAGGAAGAGAAGCA[A/G]AGATTTAAATGTCAT | 51317 |
rs773977748 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46036669 | TTGCTTTTCTGACTC[A/G]ACCATTTTTTCCACT | 51317 |
rs773978594 | snp | A/C | 3.30246e-05 | 0.0040634 | intron-variant | PHF21A | GRCh38.p7 | 11:46079176 | CAGTTTCTGGTAATA[A/C]AGAGAGAAAAAGAGC | 51317 |
rs773991430 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46065537 | TCTCCTTATTTGAAT[C/G]AATAAATTCACTTAC | 51317 |
rs773992294 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46088196 | TTCTAACAAGTTATA[A/G]ATAACAAATCAGTTG | 51317 |
rs773998675 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45969057 | TTATCTCATATTAGC[A/C]CTGCCCATCCTTCTC | 51317 |
rs774002404 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45985549 | AGTCCAGGCAAGACA[C/T]AGGATAGAATTCTAA | 51317 |
rs774003990 | snp | G/T | 1.64982e-05 | 0.00287208 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934124 | TACAGGTTTGGAGAG[G/T]TCGATGCCGTGGATG | 51317 |
rs774005618 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46014047 | TCAAGGGGTACATGT[A/G]CAGGTTTCTTATAAC | 51317 |
rs774010372 | in-del | -/AAGA | | | intron-variant | PHF21A | GRCh38.p7 | 11:45962902 | TGTCTCAAAAAAGAG[-/AAGA]GAGAACATGAAATTT | 51317 |
rs774042476 | snp | A/G | | | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46118803 | GTTTCCAACAATGCT[A/G]TAAACCAAATAAATT | 51317 |
rs774074315 | snp | C/T | 0.000158143 | 0.00889081 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45965337 | TCAAGACTTGGCTTG[C/T]TAAGCTGTACAGTTT | 51317 |
rs774104118 | snp | A/G | 1.6519e-05 | 0.00287388 | missense, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45945956 | ATTGGGGGGATGTTG[A/G]GGTAAGGGCTCCAAA | 51317 |
rs774138116 | in-del | -/TCAAGCAATCTTCTCACT | | | intron-variant | PHF21A | GRCh38.p7 | 11:45980609 | CTTGAACTCCTGGCA[-/TCAAGCAATCTTCTCACT]TCAAGCAATCTTCTC | 51317 |
rs774161941 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46050253 | CACACAGACTAATGT[C/T]GCCAGCAGCATTCCA | 51317 |
rs774167900 | snp | A/G | 3.29717e-05 | 0.00406015 | missense, utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:46076770 | TGTTTCTCACTCAAA[A/G]CTGTGATTTTGGCTT | 51317 |
rs774168704 | snp | C/T | 1.65748e-05 | 0.00287874 | synonymous-codon, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45971125 | GCTTACCAGAGTGAC[C/T]GTGTTTTTTGCCACA | 51317 |
rs774181412 | snp | C/T | 1.70977e-05 | 0.00292379 | synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45969869 | GGGGATAAACTGTGG[C/T]ACTTTGATGGGCTGA | 51317 |
rs774192349 | snp | C/G | 1.67335e-05 | 0.00289248 | intron-variant, missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45946082 | CTTACATACCTTTGG[C/G]CAGTGTTCCTCATTG | 51317 |
rs774192443 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45957105 | AGTTATAATCATATA[C/T]GTACCAGACAACAGA | 51317 |
rs774194077 | in-del | -/TTAAA | 0.00013985 | 0.00836096 | downstream-variant-500B, utr-variant-3-prime | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45928921 | CGCCATCCCTGCTAT[-/TTAAA]TTATTTAAGGTCTCT | 51317 |
rs774195293 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45942626 | TTTAGAGAATGATGA[A/T]TCTGTAACCACCAGC | 51317 |
rs774203517 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45960966 | CTGCTTCCTTGAGAT[A/G]AAGCATATTACTGTG | 51317 |
rs774203644 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45974252 | CTTAGATCTTTACCC[C/T]TACTCTGGTGCTTCT | 51317 |
rs774210709 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46029384 | ATTCCCTTTGAGTTT[A/G]AGGATTAAAAAATTC | 51317 |
rs774226367 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45935862 | CCATGAGTCCTACAA[C/T]CCAGTGCAGAGAATC | 51317 |
rs774243462 | in-del | -/GAAA | 1.64814e-05 | 0.00287061 | intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45946046 | GGAAAAACGGGGAGG[-/GAAA]GAGAGGGGGAAAATG | 51317 |
rs774248266 | snp | A/G | | | intron-variant, utr-variant-5-prime | PHF21A | GRCh38.p7 | 11:46049449 | AGTGTATTCCTGTAC[A/G]GTGGCATCTGCAAGC | 51317 |
rs774252435 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46074122 | GGTTTTGTCAGATGC[-/A]AAAAAAAAAAAAGTT | 51317 |
rs774282339 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46012422 | TATAGTCATTCCCTG[A/G]ATAACAACATTCAGT | 51317 |
rs774285576 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46002699 | CTGTCCCCGTAAAAT[A/G]TCCTATGTGTGCAAA | 51317 |
rs774296574 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46042338 | GGAGCTAGAATTTGA[C/T]GGTAAACCAGAAGAT | 51317 |
rs774297096 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45975808 | CATTGCTTTCTCTAC[A/G]CCTTGGTATATGCCA | 51317 |
rs774298482 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46027706 | AGAGCTATGAGAAGA[C/T]GCCTATTGTTCCCAT | 51317 |
rs774326426 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46106522 | TAAACAAATACTAAA[C/T]AGAATAATTCAAGTT | 51317 |
rs774327820 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46063987 | ATAAATAAAATCACA[A/T]ACTCAGAAAAACAAA | 51317 |
rs774329788 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46077789 | CATGATCACCAACTA[C/T]AACAGAAATGATAGT | 51317 |
rs774334752 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46068475 | TTCGTTATTCACACT[A/G]CCTATCACTCAAAAA | 51317 |
rs774340256 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45938547 | TGGGGAATATGTTCC[A/C]AGACCCCTAGTGGAT | 51317 |
rs774361034 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46051101 | AGCTTTCTAAAAGCA[C/T]AGTTAGTCTCTCTGA | 51317 |
rs774403837 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46015436 | CAATTTCCAGAAAAG[-/T]ATTTCCAAGGTTTTC | 51317 |
rs774422079 | in-del | -/TATA | | | intron-variant | PHF21A | GRCh38.p7 | 11:46108568 | AAATGTGTGTGTGTG[-/TATA]TATATATATATATAT | 51317 |
rs774424587 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46083249 | TGCAGCGGAACAAGA[C/G]TTTAACGAGATCCGG | 51317 |
rs774433578 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46107673 | CTTTTTATTACCTGT[G/T]TAACAAAATTTTTTA | 51317 |
rs774462249 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45949459 | TGTTCTTCTTTTTCG[C/T]TCTTGCCTCTTGCTT | 51317 |
rs774470285 | in-del | -/ATAG | | | intron-variant | PHF21A | GRCh38.p7 | 11:46078375 | GATATAGATATAGAT[-/ATAG]ATAAAGATATATTTG | 51317 |
rs774488270 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45970832 | GAGACATAAATGAAA[C/T]AGTGTGTATGCCTCT | 51317 |
rs774500468 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46083365 | AGTAGTTACCAAAGG[C/T]CCAAGATATTCTCCC | 51317 |
rs774542092 | snp | A/G | 1.68909e-05 | 0.00290606 | intron-variant | PHF21A | GRCh38.p7 | 11:45938153 | TTGGACCCACCCACA[A/G]TACCTGGTCCTGACA | 51317 |
rs774560618 | in-del | -/GT | | | intron-variant | PHF21A | GRCh38.p7 | 11:46010110 | ATGCCAAGTTTGAGA[-/GT]GTTACTGCAGGAATG | 51317 |
rs774583719 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45948425 | AAGTTCTCAAGTGTG[A/G]CTACCTCTTTCCTTC | 51317 |
rs774590351 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46116473 | CATACTCACTAAAAT[C/T]AACTACTATCACATC | 51317 |
rs774591081 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46025775 | TTTCTCTGGAATTAT[C/T]TGCAAGTCATAGGCA | 51317 |
rs774617781 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45965826 | TAGCTTTTGATTCTA[A/T]ACCCTGAGCTCCCTC | 51317 |
rs774644289 | snp | C/T | 1.75625e-05 | 0.00296327 | intron-variant | PHF21A | GRCh38.p7 | 11:45971400 | CAGATATTAGGACAC[C/T]AAATCTAAACTAAAT | 51317 |
rs774658103 | snp | A/G | 1.64798e-05 | 0.00287047 | missense, utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45979810 | ACTGCTGGGCGTGGT[A/G]GTGGTGGTACTGCTG | 51317 |
rs774663874 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46072623 | CTGAATGTCTAAATG[C/G]AATAACTATGAAGGA | 51317 |
rs774682602 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45979118 | GCCTCCTGGGTTCAA[C/G]TGATTCTCCTGCCTC | 51317 |
rs774687097 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45954941 | AAAAACACAAGCACA[C/T]AGATCTTTGATTTTC | 51317 |
rs774692186 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45995561 | ATAGAGTGGTTGAGC[A/C]GTTCATTTTTCTTTA | 51317 |
rs774705195 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45940512 | TTTAATGTTTCTTAG[C/T]AGGAAAATGTGACCA | 51317 |
rs774711264 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46081404 | TGAAAAAAGCTCTTG[A/C]TTTTCCTTTTTGATT | 51317 |
rs774724787 | snp | C/T | 1.6477e-05 | 0.00287024 | intron-variant | PHF21A | GRCh38.p7 | 11:45949362 | AGCTCATAAATAAAA[C/T]TGGAACATGAGGGAA | 51317 |
rs774734170 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46059833 | CCAGATTCAAGCAAT[G/T]CTCCTGCCTCAGCCT | 51317 |
rs774737096 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46032371 | CACTGCATAGTGTGC[C/T]ACCATGTCCTTCGTT | 51317 |
rs774752540 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46024941 | CATCATCCCTTATTA[C/T]TGAACATCCCTTCCA | 51317 |
rs774780204 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45993973 | AGGGCTAGATAACTT[A/G]CTTCAAAGTGCCAGG | 51317 |
rs774801648 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46115365 | ACATTTTTACAAAAG[A/G]TAACTATTCAAAAAT | 51317 |
rs774842816 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46038722 | TGGCGAGGTGGCTAA[A/G]CATGCTAGCATACTT | 51317 |
rs774865472 | in-del | -/TT | | | intron-variant | PHF21A | GRCh38.p7 | 11:45988525 | CTTAATATCACACTC[-/TT]GATGCTTAAAATCAT | 51317 |
rs774871906 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45956545 | ATTGCATGACGCTGA[C/G]ATTGGGGCTTCAACT | 51317 |
rs774872293 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46007554 | CCTGACCTCAGGTGA[C/T]TCGCCTGCTGTGGCC | 51317 |
rs774880884 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46022834 | ATTACCCAGGCTGGA[C/G]TGCAGTGGTGAGATC | 51317 |
rs774882080 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46097534 | AAAGAATACTAAAAT[A/G]AAGACTAAAACTATA | 51317 |
rs774929532 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46061509 | CAACATTTTGCTATT[C/T]CTGGAACTTAAAATT | 51317 |
rs774940041 | snp | C/T | 1.65913e-05 | 0.00288017 | intron-variant | PHF21A | GRCh38.p7 | 11:45936613 | AGAAGGAGGTTTAAA[C/T]ACACATCCTCTATGT | 51317 |
rs774952477 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46115103 | TGAGATATTTTCACC[-/A]AAGTCTTTTTTATTT | 51317 |
rs774957217 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45970837 | ATAAATGAAACAGTG[A/T]GTATGCCTCTGTGAA | 51317 |
rs774968066 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46096946 | CTCAGTAAATGGTAA[C/T]TCCACCCCCTCAGAA | 51317 |
rs774991493 | in-del | -/AAAC | | | intron-variant | PHF21A | GRCh38.p7 | 11:45976836 | CAGATCCTGTCTAAA[-/AAAC]AAACAAACAAACACC | 51317 |
rs775032481 | snp | C/G | 1.66882e-05 | 0.00288857 | utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:46084264 | TCTATAGTTTCTTCA[C/G]CCTCTGTTTAAAGTA | 51317 |
rs775052708 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46009518 | TGCACACATTTATTA[C/T]AGTACTTACTATAAG | 51317 |
rs775071703 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45947779 | AAATCACCAAGCACA[A/G]AACAAAACAAAACAA | 51317 |
rs775077634 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46089986 | GTGCTCAGCCCAATA[C/T]ACAGTTTCTACCTCT | 51317 |
rs775085567 | in-del | -/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45952578 | TTTTTGTGACTAGTA[-/C]TTCTTTTTGGCTTAA | 51317 |
rs775086242 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46097681 | AGACTCACTGATTAA[C/T]AGAGATCTGCTCAAA | 51317 |
rs775109076 | snp | C/T | 1.6552e-05 | 0.00287676 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45965454 | TGCCCATTGACGACA[C/T]GGACGGGGTGGATGG | 51317 |
rs775116788 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46026607 | ATTGAATGGCTGACT[A/G]TCTTTTATAATCTGA | 51317 |
rs775134599 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46035842 | AAAGAGAGGTTGGAG[-/A]AAGTAGGTATGTATC | 51317 |
rs775144882 | snp | A/G | 1.651e-05 | 0.0028731 | intron-variant | PHF21A | GRCh38.p7 | 11:46079189 | TAAAGAGAGAAAAAG[A/G]GCCATCAGTCTTACA | 51317 |
rs775148242 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46051646 | CATGCCAATGTGCAA[-/T]TTCCATTCTGTAGTA | 51317 |
rs775149496 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45955100 | CACTGGTGTTCTCTC[C/G]TATTTCCCCCTTTAT | 51317 |
rs775150412 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46102578 | CCATGAGACTAGAGA[A/G]CAGTCTAATAAATTA | 51317 |
rs775163342 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45964793 | AATGTTTCAATATTT[A/G]AGCTAAAATATCTGC | 51317 |
rs775210702 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46066560 | ATAAATTAGCCAGGC[A/G]TGACAGTGCATGCCT | 51317 |
rs775211122 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:46084244 | TCTCCACTTTCTCTG[C/T]TAATTCTATAGTTTC | 51317 |
rs775248660 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45988371 | TTAGAAAAATATATC[A/G]TAGCAGGCAGTATAT | 51317 |
rs775249373 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46007217 | GGTTCTAAGAGATGA[G/T]AAAAGGGCCCCCTGT | 51317 |
rs775303207 | snp | C/T | 1.75934e-05 | 0.00296587 | intron-variant | PHF21A | GRCh38.p7 | 11:45946105 | CCTCATTGGCTAGCA[C/T]GGAAAAGGAAGTGAG | 51317 |
rs775305439 | snp | A/G | 0.000882131 | 0.020983 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45965341 | GACTTGGCTTGCTAA[A/G]CTGTACAGTTTGAGG | 51317 |
rs775307659 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46038324 | GTAGATACGGGGTTT[C/T]ACCATGTTGGCCAGG | 51317 |
rs775314606 | snp | C/T | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45948945 | ACTGCACTCTTCTTA[C/T]GCTTTGAGGGTTGAA | 51317 |
rs775338999 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46016296 | ATGTCATTTCATGAC[C/T]CAAAATTTCCCAGAG | 51317 |
rs775368298 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46076505 | GAGTTTAATTAACAC[A/G]GTTAACGGCAGCCTG | 51317 |
rs775416874 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46050338 | TTGAAGAAAAGTGGC[C/T]GGCTTACTTTGATCA | 51317 |
rs775426868 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46014221 | TCTTTATGTCCAAGT[A/G]TACCCAATGTTTAAC | 51317 |
rs775448348 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45951044 | GCTGGTCAAAATACT[A/G]GGCCCTGAAGATGGA | 51317 |
rs775463772 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46103037 | TGGGCAATCACCGGC[A/G]GCATCTCTACACAGG | 51317 |
rs775482827 | snp | G/T | | | synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45935738 | TTTCTCTTCTTCTTT[G/T]GCTAAAAAAAAAAAA | 51317 |
rs775508814 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46065359 | CCTTTTTTGCCCCAG[C/G]ATGTTGATGTGTGAA | 51317 |
rs775517030 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46030665 | TTTTAAACAACTGCA[A/T]CATAAACATAATAAA | 51317 |
rs775565665 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46109306 | GAGGATTAAAACTAA[A/C]TAAGATCCTATGTGT | 51317 |
rs775570341 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46094617 | GAAATCCTGGCCGTG[C/T]ACAGTGGCTCATGCC | 51317 |
rs775587079 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46069472 | TTGGCTGTGAACCAC[A/G]GAGGGTAACATTTTA | 51317 |
rs775589872 | snp | A/C | | | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46120919 | AAGAGAGAATGGAAA[A/C]GCTGGGATACTGCAC | 51317 |
rs775630715 | snp | C/T | | | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46119310 | AACACAGCCACAAAG[C/T]TCACTGTCAAGGCCA | 51317 |
rs775649506 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45996810 | CAGAATAAAGTTTCC[A/G]TCATAGCAGTTTGTG | 51317 |
rs775653706 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45967471 | ACTCTCATAACTTGG[A/G]CACATCCATTGTGGG | 51317 |
rs775677055 | snp | C/G | 1.80994e-05 | 0.00300822 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45933921 | AGTCTTCAGTGTTCT[C/G]TTCTCCTTGCCGCCG | 51317 |
rs775698053 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46005808 | AAACAATTTACTCTA[A/G]CTGTATGAATCTGAT | 51317 |
rs775700917 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46116240 | GTAGTCATTTCCTTG[G/T]GCATCCTTCTAAAAT | 51317 |
rs775703789 | in-del | -/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45984599 | AGGTTCGTTTTTCCA[-/C]CGTTTAAGTCACGTT | 51317 |
rs775741369 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45966489 | CACTAAAAACAGTGA[A/G]AAAAAGTTACAGTTA | 51317 |
rs775745920 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45949907 | CCAGAAAATATAAAG[C/G]CTTATCAGAAGAGCA | 51317 |
rs775786830 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46054666 | GAGAAAAATCATTAC[C/T]ATTCAAATCACTATA | 51317 |
rs775789493 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46032497 | TTTTTCAATTCTCCA[C/G]TATTATTTAAAAAAA | 51317 |
rs775795263 | snp | C/T | 3.31279e-05 | 0.00406975 | intron-variant | PHF21A | GRCh38.p7 | 11:45950283 | GAAACAAAAGAAGAA[C/T]ATGCTTCAGTCTGGG | 51317 |
rs775798190 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46004775 | CTAAAGGACTCATCA[A/T]CTAAAAGATGTCTTT | 51317 |
rs775815335 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46020200 | TTTGTGGCATCAGTG[A/G]TGTCATTTCCTAATG | 51317 |
rs775829609 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45980426 | TGGTTAACAGTACCC[C/T]TGAGGTTCTTATGAG | 51317 |
rs775855709 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45932492 | GCCCACCAGTCTAGA[C/G]ACACACACACGGCAA | 51317 |
rs775884838 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46068550 | TACAGATATGTTCTA[C/T]GCAAAAGAAAAAAGA | 51317 |
rs775891950 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46010826 | CCCAGTGGACTGAGG[A/G]TAATAATGATCAGTT | 51317 |
rs775902891 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46047218 | TCCCTATGTAACTCA[C/T]AGGGGTGTAGGGAGG | 51317 |
rs775903690 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46033579 | CATTTTCTGTTATTA[C/T]TAACAAGGCTGCTAC | 51317 |
rs775904868 | snp | C/T | 9.95818e-05 | 0.00705556 | intron-variant | PHF21A | GRCh38.p7 | 11:45980001 | AGAAATAAAAGATAT[C/T]AGAATACTGCTCTAT | 51317 |
rs775934701 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46100674 | CATGCACAACTTTCA[C/G]TGACTATGCTTCCCC | 51317 |
rs775955831 | snp | C/T | | | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46084912 | GTCTTGATCTCCTGA[C/T]CTCGTGATCCACCCA | 51317 |
rs775961410 | snp | A/G | 1.69807e-05 | 0.00291377 | intron-variant | PHF21A | GRCh38.p7 | 11:45938337 | TGAGAGGAAAGGTAA[A/G]AAAAAGGACAAAAAA | 51317 |
rs775967254 | snp | C/T | | | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45979835 | CTGCTGCTGTTGTTG[C/T]AGTTGCTGTAGTGGT | 51317 |
rs775976012 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46018812 | TAGGAGCAGATGGTG[A/G]TAACTCACTTAATGG | 51317 |
rs776014983 | in-del | -/CTT | | | cds-indel, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45931521 | AGCCTAACTTAATTC[-/CTT]CTTCTGAGGCCCCTG | 51317 |
rs776020882 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45942073 | AACATACAGAGACCT[C/G]TGTGTTGATTTTAAT | 51317 |
rs776061193 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46102108 | TGATCCACCCGCCTC[A/G]GCCTCCCAAAGTGCT | 51317 |
rs776088482 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46050395 | TTTCCCTGTTCTGCT[A/G]ACTGTGAGCATGTTG | 51317 |
rs776103966 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45995934 | GTATATGGCTTTTTT[A/T]AAAAAAATAATTTTT | 51317 |
rs776108597 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45957167 | GATTGAGGACAGAAA[C/T]AAACAGTTCTACAAT | 51317 |
rs776111120 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45941246 | TGGGACTACAAGTGC[A/G]TACCACCATGCCCGG | 51317 |
rs776133497 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46098897 | GTGAGAACCCTTTCT[A/G]TTGCACTAACTGTAA | 51317 |
rs776142214 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46116527 | AACTGTAATAGGGGA[C/T]ATACAATTCACAGGA | 51317 |
rs776157376 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46061792 | GAATTCCCTGTTTTC[A/G]GAACCAATGCCTTCA | 51317 |
rs776161407 | snp | A/G | 1.85682e-05 | 0.00304693 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45965565 | ATGGGAGGTGGTGCT[A/G]GGGCAATAGGAATGT | 51317 |
rs776193825 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45997349 | AATATCAGAAGTGTA[C/T]TTGCAAATAACAGGA | 51317 |
rs776198718 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45972811 | CCCAGCTACTCGGGA[C/G]GCTGAGGCAAGAGAA | 51317 |
rs776217994 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45959090 | ATTTATCCCAAGAGT[C/G]GAAGGGTGGTTCAAT | 51317 |
rs776224637 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45973709 | TGTAGTAAGTGTTTT[C/T]ACCACAGTGTATTAG | 51317 |
rs776226456 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46099173 | ACAAGATTAAAACAA[C/T]CAAATTTTAAAAAAT | 51317 |
rs776231709 | in-del | -/CT | | | intron-variant | PHF21A | GRCh38.p7 | 11:46039227 | TTAAAAAGTTATCTC[-/CT]GTTTTCGTGCATTCG | 51317 |
rs776242325 | in-del | -/AAAAAAAAAA | | | intron-variant | PHF21A | GRCh38.p7 | 11:45968933 | CGAAACTCCATTGCA[-/AAAAAAAAAA]AAAAAAAAAAAAAAA | 51317 |
rs776246019 | snp | C/T | | | intron-variant, utr-variant-5-prime | PHF21A | GRCh38.p7 | 11:46075133 | ATGTCTTAACATAGA[C/T]AGTTGCAATTTTCTA | 51317 |
rs776249059 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46062561 | ATCTAGGGATCTAAA[G/T]TTATAGTTATTTTGA | 51317 |
rs776345024 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46054113 | TTTCTTGAGGCTTCT[C/T]ACCCACCAAAATGTT | 51317 |
rs776367492 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46116816 | CAAAATACAAAACTT[A/T]GCCGGGCGTAGTGGC | 51317 |
rs776410393 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45937329 | ATAGTTGAGAAAAGG[C/T]GACCAGAAACCAAAG | 51317 |
rs776435004 | snp | A/G | 1.69714e-05 | 0.00291298 | intron-variant | PHF21A | GRCh38.p7 | 11:45934243 | GCAGCAAATGACAAG[A/G]GCAGTGGCACTGAGC | 51317 |
rs776435846 | snp | A/G | 0.00018558 | 0.00963098 | intron-variant, missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45935219 | GAGCGAGGGAGGGCC[A/G]TACGGATGGGCCCAC | 51317 |
rs776445564 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46026656 | AAAATCCTTTAAAGT[C/T]AAGCAGTGGAATTAA | 51317 |
rs776504336 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46092517 | AAATGAAATGCACCT[A/C]ATTTAAATAACATAC | 51317 |
rs776520620 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45935961 | TACATAAATGAGATA[C/T]CACATCTCATTTTCT | 51317 |
rs776535588 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46025413 | TATCCCCTTTCTTCC[C/T]GCTTTAGCACCAATT | 51317 |
rs776553641 | snp | A/G | 0.000281557 | 0.0118617 | synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45965459 | ATTGACGACACGGAC[A/G]GGGTGGATGGAATTC | 51317 |
rs776576404 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46003732 | AATTTTAATTTGAAA[A/G]GTACTGGCAAGGCCT | 51317 |
rs776615441 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46091650 | AATTAACCTAAGCCA[C/G]TCTGCACATATACTA | 51317 |
rs776628737 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46042495 | AATGGTTTTTATAAA[C/T]CCTAGAAAACCGAAG | 51317 |
rs776648497 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46079555 | AAACCGGCCTGTTCA[C/T]ACACAGAGCAAAGTA | 51317 |
rs776673322 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46062679 | TTTAAGATTGAAGCG[C/G]TAAGAATGTGGAGCA | 51317 |
rs776699605 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46029474 | GGGCAGATCACTTGA[G/T]ATCAGGAGTTCAAGA | 51317 |
rs776704740 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46090178 | GAGTAAGGTATGAGA[A/G]CATAGTGACAATGAG | 51317 |
rs776710568 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46111471 | ACATGGCAAGACTCC[A/G]TCTCAAATAAATAAA | 51317 |
rs776710720 | snp | A/G | 9.88321e-05 | 0.00702896 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45949433 | GCTCCACTGTAGACC[A/G]GATTTGCTGTTGTTC | 51317 |
rs776766020 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45965179 | ACGTGGATGAATTAT[C/T]GCACATAAGCGACAG | 51317 |
rs776826224 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46094666 | AGTGGGTGGATCACG[A/G]GATCAGGAGATCGAG | 51317 |
rs776843007 | snp | A/C | 7.5543e-05 | 0.00614539 | intron-variant | PHF21A | GRCh38.p7 | 11:45935744 | TTCTTCTTTTGCTAA[A/C]AAAAAAAAAAAAAAA | 51317 |
rs776848430 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45993777 | AAATTGAAAGGGCCA[A/G]GCAGGAGAGGAGCCA | 51317 |
rs776859587 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46011000 | ACACACACACACCCC[-/T]TCTCAAAAAAGTGAT | 51317 |
rs776882376 | in-del | -/GACT | | | intron-variant | PHF21A | GRCh38.p7 | 11:45964503 | TTCAGGATCACCACA[-/GACT]ATTTTCAGATAAATG | 51317 |
rs776886739 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46108053 | TAATTAAAATATTAC[A/C]TGTATTATCTTGGTT | 51317 |
rs776896405 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45951202 | AATAATACATTATCA[A/G]TTTATTTCTCTGATG | 51317 |
rs776897485 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46108726 | AATATTTCTTGAAAG[C/G]ACACTTATCTAACAC | 51317 |
rs776898464 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45968761 | ATGACAAAACCCCGT[A/C]TCTACTAAAAATACA | 51317 |
rs776919731 | snp | A/G | 1.64808e-05 | 0.00287057 | synonymous-codon, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45971179 | CCCAGTGACCTTACT[A/G]GACGTCTGGAGGTTG | 51317 |
rs776928361 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46041618 | CAGGTCCTACCCAAT[C/T]TGTTGCTTTATAAGC | 51317 |
rs776936399 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45992581 | CATCACAAGGTGAAC[C/G]AAAAATGATTTTAGA | 51317 |
rs776940895 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46006142 | ACCAGATTAACTGAC[A/C]AGTAGATCACTGTTG | 51317 |
rs776951393 | snp | A/C | 1.66007e-05 | 0.00288098 | intron-variant | PHF21A | GRCh38.p7 | 11:45950294 | AGAATATGCTTCAGT[A/C]TGGGTTCTCACAAAG | 51317 |
rs776993478 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46058159 | CCCTACATTCTACTG[C/T]TGCCTTACCATGGGG | 51317 |
rs777037515 | snp | C/T | 1.64814e-05 | 0.00287061 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45935649 | ACACTTATGGAATTG[C/T]TGAGCTGTTTCACCT | 51317 |
rs777043591 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46035369 | TGCTAATCTGTTTGT[A/T]CCTTGCCAGCATCAT | 51317 |
rs777099713 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46056706 | GAATCAGGATTTAGC[A/G]GCAGAAATACAATGT | 51317 |
rs777117354 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46050120 | ACTGAAAGGAAATGC[C/T]TCACGCCAAGTTTTA | 51317 |
rs777118116 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46050124 | AAAGGAAATGCTTCA[C/T]GCCAAGTTTTAGAAA | 51317 |
rs777133506 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46049056 | TGACAGCTTGTGTTA[C/T]TGACAACAGGGATGA | 51317 |
rs777171351 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46069806 | TGAGTTAAATGTTAA[A/G]TGTTCTAAGCTTCTT | 51317 |
rs777222440 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46080025 | AGAAGTCCTAAAGTA[C/T]CTGGGAATAAGCTAT | 51317 |
rs777225582 | snp | A/T | 1.64738e-05 | 0.00286995 | synonymous-codon, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45971266 | CACCATAGCAATGGT[A/T]GGTCTCTGGCCCACC | 51317 |
rs777229345 | snp | G/T | 3.30218e-05 | 0.00406323 | intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45946064 | AGAGAGGGGGAAAAT[G/T]ATCTTACATACCTTT | 51317 |
rs777233913 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46030268 | GATTTCTTTAAAAGG[C/G]TGTCAAGACAATATA | 51317 |
rs777239065 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45980789 | TGTTAAACAAAGAAA[A/C]CTTGATCCCAGTAAT | 51317 |
rs777252917 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46057106 | ACTACAATTGAGAGG[-/T]TTTTTTTCCCCAAGT | 51317 |
rs777256005 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46017872 | ATTACTTTGCCTTTT[C/G]AACTCTGTAATCTCA | 51317 |
rs777261539 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45942498 | GGGACAATCTTTGGC[A/G]CTAGCAAACAAGATT | 51317 |
rs777308126 | in-del | -/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46067598 | ATATTCCACCCCCCA[-/C]AAAAAAAAAAAAAAC | 51317 |
rs777317540 | snp | A/G | 1.64741e-05 | 0.00286998 | intron-variant | PHF21A | GRCh38.p7 | 11:45948872 | GCAAGGGAGAGATAC[A/G]AAAAGGTCCTCACCT | 51317 |
rs777339363 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46084021 | ATGACTTTGTCGAGT[A/T]GTGGTAAAAGGCAAA | 51317 |
rs777372549 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45976785 | GTTTCAGTGAGCTGA[C/G]ATTGTGCCACTGCAC | 51317 |
rs777398661 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46066081 | TTCAAAAGAAAGGGA[A/T]ATAGTCTCATAAACA | 51317 |
rs777432892 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45991961 | TGATTACATTTTGCA[A/G]GACATGTAATAGGAT | 51317 |
rs777435876 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46043148 | GCCATTTGGGTCCTT[C/T]AGAGGTAAGAAATTC | 51317 |
rs777446652 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45931586 | GACACATTTTACTCT[A/G]AGAAGTGTCTCTTCT | 51317 |
rs777482858 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46094534 | TACAATAAACACTAG[C/T]GAAATATTTTTGGAA | 51317 |
rs777490263 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46080603 | TTCTTAAATCCACAT[C/T]GTAGTTTTCCAGTCC | 51317 |
rs777495429 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46104591 | CACCACGCATTTCAA[-/G]GGAGAAAAAAAACCT | 51317 |
rs777544190 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45968220 | CATCCCCAATTTATT[C/T]TCTGCACAGAGGCAA | 51317 |
rs777574822 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46070768 | CAAAATTTAAAACCA[A/G]AAGATAATTTATGGA | 51317 |
rs777618934 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45963601 | GTTTTAAAAATGAAC[-/T]TTGTACTATCTTTGT | 51317 |
rs777630398 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46006876 | ATCAACAGGTACTAA[C/T]AATATGTATTTTCAA | 51317 |
rs777646564 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46044474 | CCCATTTGGATTTCA[-/T]TATCTTATTTTCCAA | 51317 |
rs777656655 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46074459 | GTGGCTCTTTTGGCG[-/G]GGAGGGGGGAAGGCA | 51317 |
rs777679058 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46099946 | TTTTTTAAAAAATCT[C/T]TGTAGTCCAACATAT | 51317 |
rs777731972 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46020403 | GCTCTGACACTGTTC[A/G]ATGGGTCTTTGCGCA | 51317 |
rs777751919 | snp | C/T | 1.65307e-05 | 0.0028749 | intron-variant | PHF21A | GRCh38.p7 | 11:45936444 | TACTGCCAGTATTTT[C/T]TTCAAACAAGGGGAA | 51317 |
rs777786242 | in-del | -/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46038128 | TTTCTCTCTCTCTCT[-/C]TTTTTTTTTTTAAAT | 51317 |
rs777786926 | snp | A/G | 1.88642e-05 | 0.00307111 | downstream-variant-500B, utr-variant-3-prime, missense | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45928851 | CCGAGGCTGAGGCTG[A/G]GCCGGCGCTGCCCCT | 51317 |
rs777834307 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45956030 | TATATTTAAAGTGCT[A/G]AGCAAAAAAACCCCT | 51317 |
rs777854272 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:45984604 | GTTTTTCCACCGTTT[-/A]AAGTCACGTTCCATG | 51317 |
rs777863171 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46060988 | GTTCATTTTTGTATA[C/T]GGTGTAAGGAAGGGC | 51317 |
rs777865316 | snp | C/T | 1.74909e-05 | 0.00295722 | synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45965522 | GGTCAGCATGACGGG[C/T]CTCTGGATAAGCTGA | 51317 |
rs777923033 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45971727 | GTTCTTTGCTTGCTG[A/T]CAATTAATTTAAACT | 51317 |
rs777931828 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:45978314 | CAAAAAAACAATAAC[-/A]AAAAAAACAAACAAA | 51317 |
rs777936359 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45957996 | TATTGAAAAACTGTA[C/T]GCCAACAAACTAGAC | 51317 |
rs777958692 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46098810 | AGGAAGTGCCTCCTA[C/T]TAACACTAATGGGAG | 51317 |
rs777963341 | snp | A/C | 1.69706e-05 | 0.0029129 | intron-variant | PHF21A | GRCh38.p7 | 11:45938147 | CCCCTGTTGGACCCA[A/C]CCACAGTACCTGGTC | 51317 |
rs778012953 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46026164 | AATATCCAAAACTTC[A/G]TTATATTTGGCTTTA | 51317 |
rs778014730 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46009106 | CAGCCTCCTGAGTAG[C/G]TGGGATTACAGGCGT | 51317 |
rs778022407 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45976095 | CCTTATCTCCTCTCC[A/T]TCGTTTCGTGGATCA | 51317 |
rs778032298 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45973168 | ACATCAGCTCCTCAG[C/T]TGCACTAGCCACATT | 51317 |
rs778057230 | snp | A/G | 1.64811e-05 | 0.00287059 | missense, utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45979803 | GCAGCTGACTGCTGG[A/G]CGTGGTGGTGGTGGT | 51317 |
rs778062753 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46075543 | ACATACTAACCGACT[C/G]TGTTTATATTTTTTC | 51317 |
rs778065609 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46045728 | TGTTCTCTAAAACAC[A/G]TAGGTTACTAGACTT | 51317 |
rs778099867 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46043079 | CTCCTTTCCATAAAA[G/T]ATACCTGAAATTTTA | 51317 |
rs778100794 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46024831 | GAAAGAAAGACTTAG[A/G]GACTTCTTTAAGAAT | 51317 |
rs778109186 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46033753 | TAAAATATAAACACC[A/G]GATTTCAAAGACTTA | 51317 |
rs778126590 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45954210 | CCATGTTGGTCAGGC[-/T]GGTCTTGAACTCCCG | 51317 |
rs778144530 | snp | C/G | 1.75062e-05 | 0.00295852 | intron-variant | PHF21A | GRCh38.p7 | 11:45934276 | CCTGGTTTCTAACAG[C/G]CCTGGCAGCCCCTAA | 51317 |
rs778154144 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46091253 | AATTTTTTTAAAAAG[A/G]AGTAGTCTTGCACTA | 51317 |
rs778156440 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45940917 | ACATCAAGAAACAGA[A/C]GGCAGAAAGACAGAA | 51317 |
rs778182013 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46010034 | CAAAAATTTTGGGGA[A/T]GTCTGAGGAACATTC | 51317 |
rs778189027 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:45937490 | TTTATTATTAGTATT[-/A]TTTTTTTGAGACAGA | 51317 |
rs778204462 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45936886 | AGCTAGAACCACCAA[C/T]ACAAAAGCTGCACAT | 51317 |
rs778223353 | in-del | -/GAGAA | | | intron-variant | PHF21A | GRCh38.p7 | 11:46104966 | CTTGTCTCAATCCTT[-/GAGAA]GAGAAGAAAGGAGCA | 51317 |
rs778240966 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46072617 | TCACAACTGAATGTC[A/T]AAATGGAATAACTAT | 51317 |
rs778241431 | snp | A/G | 1.64942e-05 | 0.00287173 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:46084205 | AAGAGCCTCCTGTAG[A/G]GTCTGCAACTCCATC | 51317 |
rs778243879 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46089572 | AGAGCTTGGCAACCC[A/T]GATTTTCGAGGCGAA | 51317 |
rs778246926 | snp | A/G | 1.65979e-05 | 0.00288074 | synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45965393 | AGTAGCTATCACAAT[A/G]CTGGTGAGCTGGGCC | 51317 |
rs778247891 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46010060 | CATTCATTTAGTTGC[-/T]TAACCATATCATACT | 51317 |
rs778268740 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46038202 | CACAATCTCAGCTCA[C/T]TGCAACCTCTGCCTC | 51317 |
rs778281323 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46002113 | TCCAATTTACATAAG[C/T]AAATGCTTTCATTAA | 51317 |
rs778301159 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46020580 | GATGATCTAGAATAT[-/A]AAAATACTATCCTCT | 51317 |
rs778304203 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45946406 | ATTTATTTTTTGAGA[C/T]GGAATCTCGCTCTGT | 51317 |
rs778309744 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45965768 | GCATATAATCTTATA[C/T]AAGACTCATCAGCTC | 51317 |
rs778321514 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45964048 | ACTAAAAATACAAAA[A/T]TAGCCAGGCATGGTG | 51317 |
rs778329803 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45948794 | AGGATAGAGGAGTTA[C/G]GTCCTATAATGATGG | 51317 |
rs778332274 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46105992 | TTAATATTTGTATAC[C/T]AACATGTAATATACA | 51317 |
rs778342462 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46067977 | TTGCTTAAGCTGAGT[C/G]TTCAAAGGATACATA | 51317 |
rs778384121 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45985252 | ACGCTGAGGATGCAG[A/G]AAGGAGACAGGGCAG | 51317 |
rs778410992 | in-del | -/CTA | 0.000431313 | 0.0146789 | splice-acceptor-variant | PHF21A | GRCh38.p7 | 11:45935740 | TCTCTTCTTCTTTTG[-/CTA]AAAAAAAAAAAAAAA | 51317 |
rs778419675 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45947264 | TTCTAGGGGCAAGGT[C/G]ATTGCTTCTAAGCTA | 51317 |
rs778435828 | snp | A/G | 0.00018558 | 0.00963098 | intron-variant, downstream-variant-500B | PHF21A | GRCh38.p7 | 11:45935103 | CCACTTGGACAGGCC[A/G]GGCTGGGCAGTACTT | 51317 |
rs778436245 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46072246 | CTACCAGCAATAAAC[C/T]ACCTACATTTTCCAG | 51317 |
rs778450598 | in-del | -/AAA | | | intron-variant | PHF21A | GRCh38.p7 | 11:46074122 | GGTTTTGTCAGATGC[-/AAA]AAAAAAAAAAGTTGT | 51317 |
rs778471961 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46081808 | TTTATGGAAAAAAGC[C/T]ATACTCATTCATTTA | 51317 |
rs778478774 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46017032 | CTGGAGTGCAGTGGC[A/G]TGATTTTGGCTCACT | 51317 |
rs778490305 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46114564 | TTGAAGCTTCGTCAA[C/T]ACAACATACTGTCCA | 51317 |
rs778497261 | snp | A/G | | | intron-variant, downstream-variant-500B | PHF21A | GRCh38.p7 | 11:45935008 | CACTCCAACAAGGGT[A/G]ACCTACTCAATGGAA | 51317 |
rs778514162 | snp | C/G/T | 3.43049e-05 | 0.00414143 | intron-variant | PHF21A | GRCh38.p7 | 11:45938124 | TGTCTTTGTCCTCCT[C/G/T]GGCCCCTCCCCTGTT | 51317 |
rs778542167 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45948897 | TCACCTCTCTTCCGG[A/G]TCCCAGGGTGCATTG | 51317 |
rs778571454 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45983125 | TCAGCCATATGGCTA[A/G]AGCAAGGTGACGACC | 51317 |
rs778578963 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46015758 | TCAATATTACTGTCT[C/T]TTACCTCTATACCTT | 51317 |
rs778579358 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45977401 | CTCGGCCTCCCAAAG[C/T]GTTGGGATTACAGGC | 51317 |
rs778587877 | in-del | -/AAAAAAAAAAA | | | intron-variant | PHF21A | GRCh38.p7 | 11:45987668 | CCCCGTCTCAAAAAA[-/AAAAAAAAAAA]AAAAAAAAAAGCACC | 51317 |
rs778592901 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45997747 | TTGGGCCATCTGTTT[A/G]TGTGTGCTGCTTGTC | 51317 |
rs778594317 | in-del | -/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46064502 | TTCCTAAACTTGGGA[-/C]GTAAATCAACTTTGG | 51317 |
rs778595905 | snp | C/G | 1.75653e-05 | 0.0029635 | downstream-variant-500B, missense, utr-variant-3-prime | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45928835 | AGCCCCAGAGCCCTG[C/G]CCGAGGCTGAGGCTG | 51317 |
rs778600637 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45964348 | AACTAGCTTCTTGAA[G/T]GCAAGGTCTGCCGCA | 51317 |
rs778612148 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46079486 | GCATCCCTTTCAAAT[A/G]TTGTCAATGTCTAGA | 51317 |
rs778633604 | snp | C/T | 1.65411e-05 | 0.00287581 | utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:46084229 | CTCCATCCTCTACCT[C/T]CTCCACTTTCTCTGC | 51317 |
rs778634866 | snp | C/T | 3.2956e-05 | 0.00405918 | synonymous-codon, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45971299 | AGAGGCAGGCATGGT[C/T]GCAGTTGCTGCTTTC | 51317 |
rs778635544 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46051965 | ATGTGTTTCAAACTA[C/T]TAGTAGAATTCCAAA | 51317 |
rs778677045 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46019919 | CAGGGTTCCTAATAA[G/T]CTTAATCATCATGTC | 51317 |
rs778699732 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46017729 | TGATTTTGTCCCTAA[A/G]AACTGTTCTTGATAA | 51317 |
rs778708686 | snp | A/G | | | | | GRCh38.p7 | 11:46123318 | TTTTTTACTTTCGTG[A/G]CCTGCAAAATTAAGT | 51317 |
rs778711141 | snp | C/T | | | | | GRCh38.p7 | 11:45939320 | AACAATTCTCATCAC[C/T]TATCAATTCTAGGGG | 51317 |
rs778721027 | snp | A/G | | | | | GRCh38.p7 | 11:46080944 | GCTGAGATTACAGGC[A/G]TAAGCCACCATGCGC | 51317 |
rs778743545 | snp | C/G | | | | | GRCh38.p7 | 11:46044809 | GAATATATTGCCTTA[C/G]CAAAACAAACATATA | 51317 |
rs778806097 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46112791 | ATATATCAGGCTTGA[C/T]AATAAGAGGCTTCTC | 51317 |
rs778846604 | in-del | -/C | 0.000215458 | 0.010377 | intron-variant | PHF21A | GRCh38.p7 | 11:46076738 | AAAATATGCCCCCCT[-/C]CCCCTTTTCCCCTAC | 51317 |
rs778858349 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45994646 | TGGTTATGTTTTAGG[C/T]TTTGTAAGAACAAGA | 51317 |
rs778859417 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46009553 | GCACAGTTCTAAGCA[C/T]GCTATGTATTACATA | 51317 |
rs778905073 | snp | A/G | 1.65012e-05 | 0.00287234 | intron-variant | PHF21A | GRCh38.p7 | 11:45936472 | GAAGCTTACAAAAAA[A/G]TGGGTATGGATAACT | 51317 |
rs778920853 | snp | A/C | 1.65362e-05 | 0.00287538 | intron-variant | PHF21A | GRCh38.p7 | 11:45950272 | TCTGTGCCAGAGAAA[A/C]AAAAGAAGAATATGC | 51317 |
rs778921693 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46098131 | TCAGAGGGCAGATCC[A/G]TACCTTCATTTCATG | 51317 |
rs778926438 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46006909 | ATCTCAGAAAATGCA[A/T]AGTCAAAGTCAGAAC | 51317 |
rs778942844 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46089911 | GCCAGGCCAGGGTTC[C/T]CCATAGCACCCTCCT | 51317 |
rs778946324 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45993657 | TGGGGAGCTGGGCCA[A/G]CAGGGAGAGATGTCC | 51317 |
rs778969425 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45998586 | TGCGTGATCTTGGCT[C/T]GGCGCAACCTCCACC | 51317 |
rs778970235 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45938082 | AGACTGCCATTTCCC[C/G]GGGAAAGGAATTCCT | 51317 |
rs778976872 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45952427 | TGTTTATTTTTTGCA[C/G]AAACAAGGTCTCACT | 51317 |
rs778977374 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46037343 | TTCAGGCCTATTGAT[-/A]AAAAAATGGAGTGCT | 51317 |
rs778984138 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45941929 | AACACGGTACATCCA[A/G]AGGATTAGTGTCTGG | 51317 |
rs779000670 | snp | A/G | 3.32132e-05 | 0.00407499 | missense, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45945881 | ACACAGGCTGAACAG[A/G]TGCAGGGAAAGTGAA | 51317 |
rs779027357 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46046891 | CACTGCTCCCCATGA[C/T]GAAAGTTTGAGTCAA | 51317 |
rs779034128 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46007024 | TTTTAATCTTTAGAG[C/T]GTTCCTGCAAGCTCG | 51317 |
rs779062412 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45981599 | CTCATATCTCATACA[C/T]TTTCAAGTTAGTTCA | 51317 |
rs779066526 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46006203 | TTTTAAAATTAAATG[C/T]TATAAACTTCATGCT | 51317 |
rs779067518 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45997732 | TGTTCTGACTCATTG[C/T]TGGGCCATCTGTTTA | 51317 |
rs779073402 | in-del | -/CT | | | intron-variant | PHF21A | GRCh38.p7 | 11:46029515 | CAACATGGTGAAACC[-/CT]GTCTCTACTAAAAAT | 51317 |
rs779089673 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46117481 | TGCAGGCTAACTTAA[-/G]TACATCAACCATATG | 51317 |
rs779091320 | snp | A/G | | | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46084631 | AATGAGACTATAACC[A/G]TCCAGGACACACTGT | 51317 |
rs779123412 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46062312 | CATTTTCTCTGTTCC[C/T]TTGTCTCAGAACTTT | 51317 |
rs779127842 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46048364 | TCCTTTTTATTGTCA[A/T]ATAATATTCTACTGT | 51317 |
rs779142349 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46027134 | CCCAGATTATAAATA[G/T]GCTGCCAATCCAAGC | 51317 |
rs779148759 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46039755 | AATTACAGATCACTA[C/T]CAGGATCTCAGTCAA | 51317 |
rs779180143 | snp | C/T | 2.98583e-05 | 0.00386371 | downstream-variant-500B, utr-variant-3-prime, synonymous-codon | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45928903 | CCAGGGCAACCTGCC[C/T]TCCGCCATCCCTGCT | 51317 |
rs779224831 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46063090 | TGACTCAATAAACCT[A/G]TAAGAGAGAAGTGGG | 51317 |
rs779234033 | in-del | -/TC | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45933836 | CTGGCACAAGCATCT[-/TC]TCTCTCTCTCTGGAA | 51317 |
rs779238900 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46073898 | AAATCTCAAGTTACA[C/T]TTTAAAAGCACTAGA | 51317 |
rs779247731 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46010621 | ATTCATAATACTGCA[A/C]GTCAACAATCACAAA | 51317 |
rs779255289 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45960134 | GCAGTTCTTCAAATA[C/G]TTGAGCAGAATTACT | 51317 |
rs779271386 | in-del | -/TCTT | | | intron-variant | PHF21A | GRCh38.p7 | 11:46036024 | GATTCAAAAAGAAAC[-/TCTT]TAAATAAGCCAGGCA | 51317 |
rs779287493 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46089472 | TTCTTATCATTTAGC[-/A]AATTTTCAACACATC | 51317 |
rs779300647 | in-del | -/AT | | | intron-variant | PHF21A | GRCh38.p7 | 11:46024013 | GTAGCAACCTGTAAC[-/AT]ATGTGGGAACACTGA | 51317 |
rs779307585 | in-del | -/AGC | | | intron-variant | PHF21A | GRCh38.p7 | 11:45991263 | TGAATGTATCACAGT[-/AGC]AGTACCTTGATTTTT | 51317 |
rs779317310 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46075942 | ACTGGCATGAAATAT[C/G]AACTGCAAATCACCT | 51317 |
rs779340492 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45975776 | TGTTCCCATTCCCTC[A/T]CCCAAAAAGAATTCC | 51317 |
rs779343851 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46093405 | TTATACCAAACATAC[A/G]ATAAAATTATTTAAA | 51317 |
rs779355473 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46098841 | TTCTGGGTGTAAACC[A/C]TAAGCACCAAGGAGG | 51317 |
rs779384650 | snp | A/G | 4.96454e-05 | 0.00498199 | synonymous-codon, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45938301 | GCTGCAAAAATCCTC[A/G]TGAATATCACCCTAT | 51317 |
rs779403187 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46092142 | CTATCCAGCTAGCAT[C/G]AGGATCAGGCACACG | 51317 |
rs779405279 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46074376 | AAAATATCAGTCATA[C/T]GGATAAGGTAATTCA | 51317 |
rs779418356 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46026435 | ATCCTTTGCATAAAC[A/T]GGTGTCAAGGTTATT | 51317 |
rs779438406 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45989323 | AGAAGAAAAGCATGA[A/T]CGATCTCTTAATGAA | 51317 |
rs779446175 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46115105 | AGATATTTTCACCAA[A/G]GTCTTTTTTATTTAC | 51317 |
rs779449360 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45990498 | CTCCTGGACTCAAGC[A/G]ATCCACCCGCCTCAG | 51317 |
rs779461972 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45932052 | TCTCCCCAAAGGCAA[C/G]ACAGAGCGAAGGCCA | 51317 |
rs779469699 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46092382 | GAAAAAAAGAAGCAA[C/T]AGGTAATTTTTACAG | 51317 |
rs779470618 | snp | C/T | 2.55679e-05 | 0.00357538 | intron-variant | PHF21A | GRCh38.p7 | 11:45965642 | ATAATTATTGTATTA[C/T]TTAAGCTGCTCAAGT | 51317 |
rs779513275 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46074857 | GAAAATAAGTCTGAG[G/T]ACGGATGAGCTTTTG | 51317 |
rs779519473 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46109799 | CCAGTCTACCCAACA[C/T]GGTGAAACCGTCTCT | 51317 |
rs779522234 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46003573 | TGATGACATTTTCAC[A/G]AAGGGCAGAGTGAGA | 51317 |
rs779557079 | snp | A/G | 5.33338e-05 | 0.00516373 | intron-variant | PHF21A | GRCh38.p7 | 11:45935570 | CACACGTACTGTTAC[A/G]TATATTGGAAAGGCC | 51317 |
rs779565374 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46093714 | AATGCTCAATAAATG[C/T]TTGTTAAGTCAATGA | 51317 |
rs779611033 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46107653 | AAAAACTTTTATAAC[A/G]AAAACTTTTTATTAC | 51317 |
rs779629794 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46003849 | TTTCCTTTTTGAGTG[A/T]TGCAACCTAATATTC | 51317 |
rs779683986 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46040613 | AGTGCACCAAAAATA[A/G]CAGTATGTGCTGAAG | 51317 |
rs779691312 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45935354 | GGCCATGGCTACACT[C/G]TTGTAGCTGTTACTT | 51317 |
rs779720039 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46002383 | CTTCAGAAATAAACT[A/G]ATTTGTAACTTTACT | 51317 |
rs779732812 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46028604 | TTTGAGACAGAGTCT[C/T]GTTCTGTCGCCCAGG | 51317 |
rs779741877 | in-del | -/GT | | | intron-variant | PHF21A | GRCh38.p7 | 11:46030830 | TGTGCGTGTGTGTGC[-/GT]GTGTGTGTGTGTGTG | 51317 |
rs779751750 | snp | C/G | 3.30743e-05 | 0.00406645 | intron-variant | PHF21A | GRCh38.p7 | 11:45950187 | AAAAAAAGGCAGTGC[C/G]AAGAATATCTTCTCT | 51317 |
rs779766024 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46053960 | AGAACCTGCTAAAAA[G/T]TGGCAGCATCCACGA | 51317 |
rs779773972 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46039115 | AGACAACTCTAAAGA[C/T]TTGACTTTTATTCTG | 51317 |
rs779821360 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45966025 | CTCCCTGTTCTTGGC[C/T]ACTCCTCCTCTCAGT | 51317 |
rs779833383 | in-del | -/TG | | | intron-variant | PHF21A | GRCh38.p7 | 11:46108555 | AAACTTCTTTAAAAA[-/TG]TGTGTGTGTGTGTAT | 51317 |
rs779839001 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:45936380 | CCAATAGTTAAGGGC[-/A]AAAGGTTTTCATTTT | 51317 |
rs779853827 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46068125 | ATGTATGAGAATGAG[A/T]TGCTAAAGGTATCAG | 51317 |
rs779875024 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46045284 | TATTTCTTTTTCCCT[A/G]TGAAAGATCATAAGC | 51317 |
rs779884832 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46033196 | TATGGTATTCCACCA[C/T]AGGAGTGTCCCATAA | 51317 |
rs779901524 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46010132 | GCAGGAATGAGAACA[A/C]TCATTTAAAGACAAA | 51317 |
rs779924343 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46078547 | GCCTAAGTGAAAAAT[A/G]CCTATGAGAATTTAA | 51317 |
rs779951301 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45939948 | TGCTGCTGTGGATTT[C/T]CTGGCTATTCTGCCA | 51317 |
rs779951690 | snp | C/G | 1.64795e-05 | 0.00287045 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45979778 | TGAAGCAGTCAGGTT[C/G]GGAGAGGCTGCAGCT | 51317 |
rs779958949 | snp | A/G | 3.31252e-05 | 0.00406958 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45953544 | GAGGGTTCTCCTCCC[A/G]TTTTGGTTTGGGTGC | 51317 |
rs779977513 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46080986 | CTATTCTAACAACCC[C/T]GAAACCCAGCTCAAA | 51317 |
rs780038212 | snp | A/C/T | 0.000232127 | 0.0107712 | downstream-variant-500B, synonymous-codon, missense, utr-variant-3-prime | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45928842 | GAGCCCTGCCCGAGG[A/C/T]TGAGGCTGGGCCGGC | 51317 |
rs780038776 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46111255 | GGGCAGATCACTTGA[A/G]GCCAAGAGTTAAGAG | 51317 |
rs780039605 | snp | C/T | 6.59011e-05 | 0.00573988 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45979883 | TAGTTTGTTTTCAGA[C/T]TGTGGCAATGGCTGT | 51317 |
rs780046912 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46078037 | CTGCCTCAGCCTCCT[A/G]AGTAGCTGGCCTTAC | 51317 |
rs780071526 | snp | C/T | 1.76434e-05 | 0.00297008 | intron-variant | PHF21A | GRCh38.p7 | 11:46076890 | GTAGCAGGAAGACTA[C/T]GCATACTGCATTACA | 51317 |
rs780101552 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45978611 | TGTAAGAGGTATCCA[C/T]GCTTAGGTTTCAGAG | 51317 |
rs780103506 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45996482 | CATCCTTGACAGTGG[C/T]CACATAAATGATTTC | 51317 |
rs780121322 | in-del | -/AAATGAAGACAA | 1.65042e-05 | 0.0028726 | intron-variant | PHF21A | GRCh38.p7 | 11:45979972 | CTACTCTTTTCTACC[-/AAATGAAGACAA]AAAGAAATAAAAGAT | 51317 |
rs780126198 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45985068 | TCAGACACACCAATT[A/G]CTCAAAATGAAACCA | 51317 |
rs780150629 | snp | C/T | 6.59446e-05 | 0.00574177 | missense, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45971319 | TTGCTGCTTTCAAGA[C/T]GAGAGGTAGTGTCTT | 51317 |
rs780157516 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46058070 | CTCAACTTTTAACAA[A/C]GCCTTGTTAAATGTG | 51317 |
rs780192879 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45994976 | TAACTCCATCTTGAG[A/C]CCACAGAAATGTGTA | 51317 |
rs780196213 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46034665 | GTGGCTATCTATGGC[C/T]GTGCTACTCGCCTCC | 51317 |
rs780218963 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45950761 | AAAATCCTCTTAAAA[A/G]GAAGAGGATTTCATA | 51317 |
rs780253152 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46115749 | ATTAAAGGTCAGAGA[A/C]CTAAAACTTTAATTC | 51317 |
rs780253626 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46036015 | AAGCAAGAAGATTCA[A/G]AAAGAAACTCTTTAA | 51317 |
rs780270638 | snp | C/T | 1.65201e-05 | 0.00287398 | intron-variant | PHF21A | GRCh38.p7 | 11:46076730 | ACAACGTTAAAAATA[C/T]GCCCCCCTCCCCTTT | 51317 |
rs780273754 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46013281 | TTTTAAACTGCACGC[C/T]TAGAGTAGCCTGACG | 51317 |
rs780274403 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46050012 | TGTAGTCACCACATG[C/T]TCAATTTGCTGTAGG | 51317 |
rs780333766 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45975312 | CAGTGAGACCCTGTC[C/T]CAAAGAAAACAAAAT | 51317 |
rs780344547 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46070880 | ATACATCTTCCAAAT[G/T]AGCAGAGTGCTTTTT | 51317 |
rs780346786 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46088778 | ATAGAACTTCTCTAC[A/G]TAGTATATATCTAGA | 51317 |
rs780374392 | in-del | -/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46029444 | TGTAATCCTAATACA[-/C]GGGGAGGCCAAGGCG | 51317 |
rs780374414 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45985913 | ATAGTACAAATAAAC[A/C]AATTGACAACAGCAG | 51317 |
rs780379759 | snp | A/T | | | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46085484 | TTCTTTTCTTGAATG[A/T]GGCCTTAGACATGAT | 51317 |
rs780389428 | in-del | -/TT | | | intron-variant | PHF21A | GRCh38.p7 | 11:46112910 | GTTTTCAATATATTA[-/TT]TTGTGTGTAAACCTT | 51317 |
rs780397923 | in-del | -/AC | | | intron-variant | PHF21A | GRCh38.p7 | 11:45958449 | TATATATATATATAT[-/AC]ACACACACACACACA | 51317 |
rs780423906 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45969365 | TTTAGAAGCAAGGCT[C/T]TGCCTTTAAGCATGA | 51317 |
rs780428688 | snp | C/T | 3.54925e-05 | 0.00421248 | intron-variant | PHF21A | GRCh38.p7 | 11:45969776 | TGAGGATTTCTGTCC[C/T]ATCTAACCTATCATT | 51317 |
rs780436644 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46087142 | CTTCTTTTTGGGGTA[C/T]TGATATTTTCAAAAT | 51317 |
rs780464054 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45997936 | AAAAAAGTGATACAC[A/C]ACAGGCCCATGTGCA | 51317 |
rs780471778 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46005800 | CAATTCTGAAACAAT[C/T]TACTCTAGCTGTATG | 51317 |
rs780474268 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46089212 | TTGACAGTCATCTAC[A/G]TATCTTTACTTCTTG | 51317 |
rs780499969 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45943567 | ATAGGCCCTTTTCTT[C/T]TGCATATTTTAGACA | 51317 |
rs780512254 | in-del | -/AA | | | intron-variant | PHF21A | GRCh38.p7 | 11:46118419 | AAAAGTCTGATGTTA[-/AA]AAAAAAAAAAAAAAA | 51317 |
rs780516520 | snp | C/T | 1.65534e-05 | 0.00287688 | missense, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45945910 | AATGTGGTCTCTGTC[C/T]TTTCATTTTCAGGGG | 51317 |
rs780540438 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46062418 | TCTTCCATCTATTTA[C/T]TGAGAAACAACTCCA | 51317 |
rs780550168 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46011970 | CTCTATCTAGATTTC[C/T]AGATGACTATCACCT | 51317 |
rs780563949 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45987569 | GGGAGGCTGAGGCAG[A/G]AGAATTGCTTTAACC | 51317 |
rs780584044 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46021733 | TATTTTATTTTTTTG[C/T]AGAGATGAGATCCCA | 51317 |
rs780589698 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45960353 | CATGTCATGGAATAT[A/T]ATTCAGCCATTTAAA | 51317 |
rs780597546 | snp | A/G | 0.000371058 | 0.0136158 | intron-variant, synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45935223 | GAGGGAGGGCCGTAC[A/G]GATGGGCCCACTCGC | 51317 |
rs780609372 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46116486 | ATCAACTACTATCAC[A/G]TCACATCAATGGAGA | 51317 |
rs780610883 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46077466 | AAAGTAGGCAAAAAA[C/T]TCCAAAATTAAAGTT | 51317 |
rs780613105 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46077213 | ACACACTACATGCTT[C/T]ACAGCATTATCAACA | 51317 |
rs780614009 | snp | C/T | | | intron-variant, utr-variant-5-prime | PHF21A | GRCh38.p7 | 11:46117942 | ATCTTTCTGGAACTT[C/T]AAGGTGTTAATCCTG | 51317 |
rs780614548 | snp | A/G | 1.71602e-05 | 0.00292913 | missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934017 | GTGCAGCTCTGGGAG[A/G]AGGGGGAAGGGGCCG | 51317 |
rs780641317 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46042216 | TTGGGGCCTGTGGGA[A/T]AGCCACATGACAAAA | 51317 |
rs780646685 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46104943 | AAGCTCAGGCTCTTA[C/T]ACTAATACTTGTCTC | 51317 |
rs780671901 | in-del | -/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45932676 | ATTTAAGTAACACTA[-/G]GAAGACCTCAATATC | 51317 |
rs780672781 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45991654 | CTGTAAAAATAATAC[A/G]CTGGGTCGAGAAACC | 51317 |
rs780675818 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45958882 | GCAATTGTACCACTA[C/T]ACTCCAGTCTGGGTA | 51317 |
rs780689025 | in-del | -/TC | | | intron-variant | PHF21A | GRCh38.p7 | 11:46089016 | TCATCAACCAACATT[-/TC]TTTAACTAACGATAA | 51317 |
rs780707606 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46079355 | CCTTTAATAAAAAAA[C/T]CAAACCACCACTTTA | 51317 |
rs780736986 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46027235 | CTACAAGTTTTCTCC[A/G]TGCTAACAGGTACAA | 51317 |
rs780781263 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45991823 | TGTATATCTTTACCT[C/T]TATAGCACTGCACAG | 51317 |
rs780826635 | in-del | -/AAGTA | | | intron-variant | PHF21A | GRCh38.p7 | 11:46118705 | ACCGATTCCATAAAC[-/AAGTA]AAGACAGAAGAAGAG | 51317 |
rs780839518 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46040333 | TACAGTGATGACACT[A/G]CTGGTAGTTATAAAC | 51317 |
rs780886526 | snp | G/T | 1.73634e-05 | 0.00294642 | intron-variant | PHF21A | GRCh38.p7 | 11:45935578 | CTGTTACGTATATTG[G/T]AAAGGCCTAGGTCTC | 51317 |
rs780919922 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46040931 | CACACACACACACAC[A/G]CACGCACGCACAATT | 51317 |
rs780955827 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46088526 | TATCTGGAAAGCACA[-/T]TCACCATCCCAAAAA | 51317 |
rs780960207 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45981091 | TATACTCTGCACTTA[C/T]AACTATATTGCTGGC | 51317 |
rs780990489 | in-del | -/T | | | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46084682 | CAACAGAATCATAAT[-/T]TTTTTTTTTTTTTTT | 51317 |
rs781007896 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46055428 | GATGGGAAAAGTGTA[C/G]AGTACACAGTAACCC | 51317 |
rs781042097 | in-del | -/GAT | | | intron-variant | PHF21A | GRCh38.p7 | 11:46062052 | AGAAGTCTGATGACA[-/GAT]TCTGATTCCCAATCC | 51317 |
rs781051933 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45929965 | AGAGCAAAGTTGCCT[C/T]CACTCAACAGAAGCC | 51317 |
rs781064263 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45950449 | CTTGGCTTCCTTCAA[C/T]GTGGGCCACATTGGA | 51317 |
rs781082525 | snp | G/T | 1.64863e-05 | 0.00287104 | synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45950222 | TTCTAGATGGTCATG[G/T]GTTACCAACCCTAGA | 51317 |
rs781086607 | in-del | -/GTGA | | | intron-variant, downstream-variant-500B | PHF21A | GRCh38.p7 | 11:45935005 | TTCACTCCAACAAGG[-/GTGA]GTGACCTACTCAATG | 51317 |
rs781092948 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46114525 | TACATTTCACCATAA[A/C]AGTGACGGGCTACTA | 51317 |
rs781095484 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45960552 | GCAAAAGTTAAATAA[-/T]TGCTTAATGGATACT | 51317 |
rs781123066 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46068408 | GCACATTATTTGAAA[A/G]CACATGATATAGTAG | 51317 |
rs781140277 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46100536 | TAATTTTTAAAATAT[A/G]TATCTTTGGTGTAGA | 51317 |
rs781158015 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46107535 | ATTCTACCAGGTCCA[A/G]TTCTTAGAATTTTAC | 51317 |
rs781182355 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45955923 | GTAGCACAGCCTTAA[A/T]ATTACTGCAGCTCTA | 51317 |
rs781223912 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46039952 | TTAAAAACCCTCAAA[G/T]GAGTTTATTCTTATT | 51317 |
rs781233674 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46031913 | ATTATCAGGTACAAG[A/G]AACTGGATTGGATTG | 51317 |
rs781245313 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45979698 | ACAGGACCCAGTTCT[A/G]TATGACCAACAACAA | 51317 |
rs781257945 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45938727 | ATGGGAATGAGGTCT[A/G]TCTTCTTTTTTCTTT | 51317 |
rs781272372 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45954378 | ACATCTCACATACAC[A/G]GTCTCCTATTTCGGA | 51317 |
rs781273810 | snp | A/G | 0.000567783 | 0.0168395 | intron-variant | PHF21A | GRCh38.p7 | 11:46084145 | AACAACAGTGTGGGA[A/G]AAGCCAATAATACAA | 51317 |
rs781277394 | snp | C/T | 1.64757e-05 | 0.00287012 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45979913 | TATTTGGAACTTGTC[C/T]GGTTGTTCTTGCTTT | 51317 |
rs781307421 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46033303 | ACAGTCTTACTCTGT[G/T]GCCTAGATTGGAGTG | 51317 |
rs781323165 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45985102 | ATACTAAATTTTACG[C/T]GTATGGAAAAACTAA | 51317 |
rs781324104 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46008804 | CTGCAAAATGCTATG[G/T]TTGCAACTGTAAAAT | 51317 |
rs781350738 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45971525 | TCTTTTGTGTACATA[C/T]AGCATACTCCTTACT | 51317 |
rs781412413 | in-del | -/AC | | | intron-variant | PHF21A | GRCh38.p7 | 11:45991559 | GCAGTAAGCTTATAC[-/AC]ACACACACACACATG | 51317 |
rs781414309 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46024790 | GGGTGACCAAGTGAG[A/C]CTCCATCTCAAAAAA | 51317 |
rs781430528 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46097596 | TATGCTCTTCCTTAT[A/G]ACAAGAATAATACCT | 51317 |
rs781450296 | in-del | -/CTCT | | | intron-variant | PHF21A | GRCh38.p7 | 11:45982374 | TTCTGCTAGCACTGC[-/CTCT]CTGAGTAAATATTTT | 51317 |
rs781459980 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46104048 | CTTATGACAATTAAA[C/T]ATAGAAAGAAAATAA | 51317 |
rs781489702 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46105749 | CCAAATTTTACATTT[-/A]AAAAAGCACTAGGCC | 51317 |
rs781512705 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46051337 | GCATGTCATTTCAGT[G/T]CTGCCTGGGGGCCCA | 51317 |
rs781514492 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46025544 | CCTTTACCTGAGAAG[-/A]AAAATGATTCTCTGG | 51317 |
rs781515260 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45936186 | GGGAGGCTGAGGTAG[A/G]AGGATCGACTGGGCC | 51317 |
rs781543906 | snp | A/G | 1.64833e-05 | 0.00287078 | intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45946050 | AAACGGGGAGGGAAA[A/G]AGAGGGGGAAAATGA | 51317 |
rs781557312 | in-del | -/TGT | 1.64852e-05 | 0.00287094 | cds-indel, utr-variant-5-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45979826 | TGGTGGTACTGCTGC[-/TGT]TGTTGTTGTAGTTGC | 51317 |
rs781558985 | snp | C/G | 3.29495e-05 | 0.00405877 | intron-variant | PHF21A | GRCh38.p7 | 11:45948855 | AAGCAAAAGCAACAG[C/G]AGCAAGGGAGAGATA | 51317 |
rs781612038 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45978589 | ACAGTGAAGACCTGG[C/T]GTTGGTTGTAAGAGG | 51317 |
rs781656462 | in-del | -/AGAAGGGAAC | | | intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45946016 | GACCTATATACCAAG[-/AGAAGGGAAC]AAAAGGGAAAAACGG | 51317 |
rs781661877 | snp | C/T | 1.91254e-05 | 0.0030923 | intron-variant | PHF21A | GRCh38.p7 | 11:46079104 | TATTTTTAAATTTAA[C/T]AATTAAATGAATAAC | 51317 |
rs781662340 | snp | C/T | | | upstream-variant-2KB | PHF21A, LOC105376661 | GRCh38.p7 | 11:46122827 | AGCTTAACGTTTTTG[C/T]ATGGATGTATTACCG | 51317 |
rs781691014 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46034242 | CCCTTGCATACTTTT[C/T]CCTTGGGAGGCTCAT | 51317 |
rs781708736 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45961607 | TCCCCACAGAACCTT[A/G]GGATTTTTTTCAGTA | 51317 |
rs781714946 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46102202 | GATACACCAGCCTCG[G/T]CCTCCCACAGTGCTG | 51317 |
rs796090203 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45968065 | TAATACCTATTTGCA[C/T]AGGGTTGTTGTAACA | 51317 |
rs796110725 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46075812 | ATAGAAACACAATAA[A/C]AAATCTCCAGAAATG | 51317 |
rs796113519 | in-del | -/AAAAAAAAAAAAAA | | | intron-variant | PHF21A | GRCh38.p7 | 11:45935742 | TCTTCTTCTTTTGCT[-/AAAAAAAAAAAAAA]AAAAAAAAAGGAACG | 51317 |
rs796117787 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46113843 | AAAAAAAAAAAAAAA[-/A]GTTTAATTGTTTTAA | 51317 |
rs796120212 | in-del | -/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46105386 | GGCACACAGGACATG[-/C]CCCTGATGATTAGAT | 51317 |
rs796145239 | in-del | -/ACAC | | | intron-variant | PHF21A | GRCh38.p7 | 11:46040931 | CACACACACACACAC[-/ACAC]GCACGCACAATTAAG | 51317 |
rs796156441 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45998842 | GTTTTTGTTTTTTTT[-/T]GAGACAGTCTCACTC | 51317 |
rs796201216 | in-del | AA/TTATGATTTT | | | intron-variant | PHF21A | GRCh38.p7 | 11:45940659 | CTTCCTTCATTATTA[AA/TTATGATTTT]ATCAGGCTGAGGGCT | 51317 |
rs796258958 | multinucleotide-polymorphism | ATC/TCT | | | intron-variant | PHF21A | GRCh38.p7 | 11:45962687 | CCTGAGGTCAGGAGT[ATC/TCT]AGACCAGCCTGGCCA | 51317 |
rs796262576 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46056169 | TTTGAATTTCATCTT[A/T]TAAGGAGAAAACAGA | 51317 |
rs796287390 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46056975 | AGATAACTGATTTTA[C/T]TTGCTTTAAATATAG | 51317 |
rs796333792 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45997492 | GATGAAGCCAGCCCA[C/T]GCCTACGTGAAACAG | 51317 |
rs796368678 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46094792 | GTAATCTCAGCTACT[C/T]GGGAGGCTGTGACAG | 51317 |
rs796369561 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46072005 | TCTGTGTTAATATTC[C/T]ATGTTAAATATTATA | 51317 |
rs796424142 | in-del | -/AAAAA | | | intron-variant | PHF21A | GRCh38.p7 | 11:45957752 | AACTAAATTCAAAGC[-/AAAAA]AAAAAAAAAAAAAGA | 51317 |
rs796470316 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45983980 | CTGCTGGTCACTGAC[A/G]AAGGTTATACTGGCA | 51317 |
rs796511402 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46092109 | CAAAAAAAAAAAAAA[-/A]TCACAATATTTGAAT | 51317 |
rs796525216 | multinucleotide-polymorphism | CA/TG | | | intron-variant | PHF21A | GRCh38.p7 | 11:45962657 | GCACTTTGGGAGGCC[CA/TG]GGCAGGTGGGTCGCC | 51317 |
rs796537451 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46057269 | AACTCAGCTATAATC[C/T]TTGCATGTCTATAAG | 51317 |
rs796541998 | in-del | -/TA | | | splice-acceptor-variant | PHF21A | GRCh38.p7 | 11:45935741 | CTCTTCTTCTTTTGC[-/TA]AAAAAAAAAAAAAAA | 51317 |
rs796635442 | snp | A/G | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46118787 | TAAAAATGTAGTAAC[A/G]GTTTCCAACAATGCT | 51317 |
rs796636730 | in-del | -/AAAAAAAAAAA | | | intron-variant | PHF21A | GRCh38.p7 | 11:45981409 | AAAAAAAAAAAAAAA[-/AAAAAAAAAAA]CTATATTGCTCAGTA | 51317 |
rs796663244 | in-del | AGGATCAC/TGGGTCGCCT | | | intron-variant | PHF21A | GRCh38.p7 | 11:45962666 | GAGGCCAAGGCAGGT[AGGATCAC/TGGGTCGCCT]AGGTCAGGAGTCTGA | 51317 |
rs796695122 | in-del | -/AC | | | intron-variant | PHF21A | GRCh38.p7 | 11:45955308 | cacacacacacacac[-/AC]TTTTTAATCAAAAAG | 51317 |
rs796702985 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46106820 | GGCAGGCAGCCCTTT[A/C]CCTTTTGGTCAACTC | 51317 |
rs796763448 | in-del | -/AAAAAAAAAAAAA | | | intron-variant | PHF21A | GRCh38.p7 | 11:45968932 | GCGAAACTCCATTGC[-/AAAAAAAAAAAAA]AAAAAAAAAAAAATA | 51317 |
rs796825130 | in-del | -/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46091840 | ctataggcacacacc[-/C]actgggcctggcTGG | 51317 |
rs796825731 | in-del | -/TTTC | | | intron-variant | PHF21A | GRCh38.p7 | 11:45971882 | AAAGGACAGTGTCTT[-/TTTC]TTTCTTTCTTTTTTT | 51317 |
rs796850119 | in-del | -/GA | | | intron-variant | PHF21A | GRCh38.p7 | 11:46074461 | TGGCTCTTTTGGCGG[-/GA]GGGGGGAAGGCATAT | 51317 |
rs796892141 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45981422 | AAAAAAAAAAAAACT[A/G]TATTGCTCAGTAAAT | 51317 |
rs796896102 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:45970023 | ACAAGCTTTCATCGT[-/A]AGTTAATCATCTGAA | 51317 |
rs796901322 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46049966 | GTGATTAACTCAATC[A/G]AAGTAGGACCATATT | 51317 |
rs796904074 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46086408 | ACAGGCATGAGCCAC[C/T]GCACCCAGCCAGCTA | 51317 |
rs796915756 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46071949 | GCAGAGCAAAAGATC[A/G]GGTGGATAAAATAAT | 51317 |
rs796953961 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46059697 | AAAGTGCTAGGATGA[A/C]AGGCATAAGCCATTG | 51317 |
rs796966436 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45944960 | TAGAGACCAGGTTTC[A/G]CCATGTTGGCCAGGC | 51317 |
rs796974742 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45957946 | AAACTGAGGACATTA[C/T]ATCTCACAGAATTCA | 51317 |
rs796991359 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46049857 | TCCTAAAAACAACGT[-/T]AAGACTATCCAGCAA | 51317 |
rs796991509 | snp | C/T | | | intron-variant, downstream-variant-500B | PHF21A | GRCh38.p7 | 11:45934725 | GAGACGACAGGCCAG[C/T]AGCATTTAGGAGGAT | 51317 |
rs796996763 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46016971 | AATGTTTAACCTGGA[-/T]TTTTTTTTTTTTTAA | 51317 |
rs797004993 | in-del | -/ATTATT | | | intron-variant | PHF21A | GRCh38.p7 | 11:45974449 | ATTATTATTATTATT[-/ATTATT]GCTGTTTATTTATTT | 51317 |