SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs923530 | snp | G/T | 0.496314 | 0.0427728 | intron-variant | PHF21A | GRCh38.p7 | 11:46087968 | CGCCATGTTGCCTAG[G/T]CTGGTCTTGAGCTCC | 51317 |
rs939106 | snp | A/C | 0.217851 | 0.247924 | intron-variant | PHF21A | GRCh38.p7 | 11:45954709 | ACTGAAATAATTTTA[A/C]AACAGAAAATATCAA | 51317 |
rs939107 | snp | A/G | 0.491157 | 0.065903 | intron-variant | PHF21A | GRCh38.p7 | 11:45960800 | CATGATGCAGACTCG[A/G]AATTGTCTTGCAGAT | 51317 |
rs950105 | snp | A/T | 0.472241 | 0.114494 | intron-variant | PHF21A | GRCh38.p7 | 11:46115871 | CTTAACTTCAGTATG[A/T]CTTCACAGAAAGCTT | 51317 |
rs953230 | snp | A/G | 0.484771 | 0.0859212 | intron-variant | PHF21A | GRCh38.p7 | 11:46043423 | AATTAATCCTTTCTG[A/G]TTAACATACTACCTT | 51317 |
rs953577 | snp | G/T | 0.0755793 | 0.179102 | intron-variant | PHF21A | GRCh38.p7 | 11:46054967 | TACCTAAGCATTTTA[G/T]TTTAGTTTAAATGAA | 51317 |
rs959241 | snp | A/C | 0.0898077 | 0.191933 | intron-variant | PHF21A | GRCh38.p7 | 11:46097373 | ccagtgttgctggaa[A/C]ggattgagcgatagg | 51317 |
rs1006909 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | PHF21A | GRCh38.p7 | 11:46113121 | TTGATTTAAACAGTA[C/T]GGAAAACCCTTCCTT | 51317 |
rs1038733 | snp | A/G | 0.167158 | 0.235875 | intron-variant | PHF21A | GRCh38.p7 | 11:46075867 | ACTAAATAACATTAA[A/G]TAACAACATAAAAAT | 51317 |
rs1063809 | snp | A/G | 0 | 0 | missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934030 | GCCACCTCCACGCCG[A/G]CCCCTTCCCCCTCCT | 51317 |
rs1063810 | snp | C/G/T | 1.69232e-05 | 0.00290883 | missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934029 | CCACCTCCACGCCGG[C/G/T]CCCTTCCCCCTCCTC | 51317 |
rs1125290 | snp | C/G | 0.489318 | 0.0722982 | intron-variant | PHF21A | GRCh38.p7 | 11:45985503 | TCCAGTGCAGATTCT[C/G]TTATTGAATTTTACT | 51317 |
rs1125291 | snp | C/T | 0.491368 | 0.0651254 | intron-variant | PHF21A | GRCh38.p7 | 11:45985186 | TGAGTTTTAGTTAGA[C/T]GGTAGAAAGTCTTTT | 51317 |
rs1132657 | snp | A/C | | | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46119371 | GTATGGATTTCTAGA[A/C]TTTCAAATCTGAGTG | 51317 |
rs1135457 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46019316 | GATTCATTTGACATG[A/G]TACTTAATTTTGATG | 51317 |
rs1135458 | snp | A/C | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46019233 | CGACATTCTTTTCCC[A/C]TATCTTCTAGAAAGA | 51317 |
rs1352643 | snp | A/C | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46044290 | TTAAACCAAATGTAC[A/C]TTAAATGAGCAGGAA | 51317 |
rs1401420 | snp | C/G | 0.204803 | 0.245881 | intron-variant | PHF21A | GRCh38.p7 | 11:45961081 | AAAAGCGGGATATCT[C/G]TTATACTCATGTTCC | 51317 |
rs1401421 | snp | A/G | 0.205723 | 0.246048 | intron-variant | PHF21A | GRCh38.p7 | 11:45984278 | AAACAATAAGCCAAC[A/G]TGCCAGGCCTCCAGA | 51317 |
rs1490082 | snp | C/T | 0.167809 | 0.236103 | intron-variant | PHF21A | GRCh38.p7 | 11:46117734 | GTGGGATGTTGAGCA[C/T]GTATTTTAAAAAATT | 51317 |
rs1490087 | snp | A/G | 0.16846 | 0.236329 | intron-variant | PHF21A | GRCh38.p7 | 11:46086859 | ACATAACAAAGGGCT[A/G]ATACAGTTTATATAT | 51317 |
rs1490088 | snp | C/T | 0.133777 | 0.221342 | intron-variant | PHF21A | GRCh38.p7 | 11:46086891 | TAGGGCCCTCAAAAA[C/T]TGATAACAAAAATCT | 51317 |
rs1490089 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46086899 | TCAAAAATTGATAAC[A/C]AAAATCTATGAAAAA | 51317 |
rs1542724 | snp | G/T | 0.272511 | 0.248984 | intron-variant | PHF21A | GRCh38.p7 | 11:46095632 | ATATTATAACCATAT[G/T]AGAAATCTGGATGAT | 51317 |
rs1554339 | snp | C/T | 0.206029 | 0.246103 | intron-variant | PHF21A | GRCh38.p7 | 11:45984949 | GAATCAACATGCAAT[C/T]TAAAAATACAACCTT | 51317 |
rs1565412 | snp | C/G | 0.463881 | 0.12944 | intron-variant | PHF21A | GRCh38.p7 | 11:46064596 | AAGATACTAGTTAAA[C/G]AGTAAACTTCTTTTT | 51317 |
rs1907003 | snp | C/T | 0.168135 | 0.236216 | intron-variant | PHF21A | GRCh38.p7 | 11:46066944 | AATACTGAATTATAC[C/T]GTATGTCTGTTTTAC | 51317 |
rs1973721 | snp | A/G | 0.206029 | 0.246103 | intron-variant | PHF21A | GRCh38.p7 | 11:45972868 | tgagtgcagtggcac[A/G]atttctgctcactgc | 51317 |
rs1976182 | snp | A/C | 0.471958 | 0.115042 | intron-variant | PHF21A | GRCh38.p7 | 11:46070393 | TGGAGTGCAGTGGCA[A/C]CATCTTGGCTCCCTG | 51317 |
rs1994599 | snp | A/C | 0.167809 | 0.236103 | intron-variant | PHF21A | GRCh38.p7 | 11:46068872 | GCATCTGGTACAAGT[A/C]ACCAACTGACTTGAT | 51317 |
rs1996573 | snp | C/G | 0.470715 | 0.117409 | intron-variant | PHF21A | GRCh38.p7 | 11:45953092 | ATACAATGGTTGTAA[C/G]AAAAACGCACACTTA | 51317 |
rs2013010 | snp | C/G | 0.463126 | 0.13068 | intron-variant | PHF21A | GRCh38.p7 | 11:46059707 | gatgacaggcataag[C/G]cattgtacctggccT | 51317 |
rs2056261 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45981468 | ACCTGATGTGTAAAG[G/T]GGTGGGACCAAAGAC | 51317 |
rs2056262 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45981471 | TGATGTGTAAAGTGG[G/T]GGGACCAAAGACCAA | 51317 |
rs2130469 | snp | A/G | 0.16846 | 0.236329 | intron-variant | PHF21A | GRCh38.p7 | 11:46087381 | TTTACTTTCTCCATC[A/G]GATTGTTGTCTGCTT | 51317 |
rs2130470 | snp | C/T | 0.167809 | 0.236103 | intron-variant | PHF21A | GRCh38.p7 | 11:46087624 | GAAAGAAACAAATTA[C/T]AGACATGTATTTATA | 51317 |
rs2130471 | snp | C/T | 0.167484 | 0.23599 | intron-variant | PHF21A | GRCh38.p7 | 11:46091423 | GAGCCATTAAAAAAA[C/T]CTCTCAAAGTAGATA | 51317 |
rs2130473 | snp | C/T | 0.167484 | 0.23599 | intron-variant | PHF21A | GRCh38.p7 | 11:46094668 | GTCTCGATCTCCTGA[C/T]CTCGTGATCCACCCA | 51317 |
rs2130475 | snp | C/T | 0.384017 | 0.211044 | intron-variant | PHF21A | GRCh38.p7 | 11:46107488 | GGCTGGTAAAAAACG[C/T]TGACTACTCTATAGT | 51317 |
rs2130476 | snp | A/G | 0.384017 | 0.211044 | intron-variant | PHF21A | GRCh38.p7 | 11:46107551 | TTCTTAGAATTTTAC[A/G]GCAAGGCTTTAGCAC | 51317 |
rs2171895 | snp | C/T | 0.168135 | 0.236216 | intron-variant | PHF21A | GRCh38.p7 | 11:46091564 | AGACATGAAGCTAAC[C/T]AATCCAATATTAATT | 51317 |
rs2220546 | snp | A/G | 0.395453 | 0.203331 | intron-variant | PHF21A | GRCh38.p7 | 11:46072994 | TCAAAAAATCAGGGT[A/G]TGGGGAGTGAGAATG | 51317 |
rs2860376 | snp | G/T | 0.216649 | 0.247765 | intron-variant | PHF21A | GRCh38.p7 | 11:45951910 | CTCCTGGGTTCAAGC[G/T]ATTCTCCAGCCTCAG | 51317 |
rs2860403 | snp | C/T | 0.167809 | 0.236103 | intron-variant | PHF21A | GRCh38.p7 | 11:46074462 | ATATGCCTTCCCCCC[C/T]CCCGCCAAAAGAGCC | 51317 |
rs2860404 | snp | A/G | 0.485528 | 0.0838238 | intron-variant | PHF21A | GRCh38.p7 | 11:46074016 | CTCAGTTTCTCCCTT[A/G]AAACTATGTAATCGT | 51317 |
rs2860433 | snp | C/T | 0.205417 | 0.245993 | intron-variant | PHF21A | GRCh38.p7 | 11:45977045 | ACACTGTTTTGGAGG[C/T]AGCCCTGGGCCTCTT | 51317 |
rs2863714 | snp | A/G | 0.185472 | 0.241529 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930760 | CTCTCTGAAGTGACT[A/G]CAAAGCCAGCTGGTC | 51317 |
rs2902550 | snp | C/T | 0.168135 | 0.236216 | intron-variant | PHF21A | GRCh38.p7 | 11:46058348 | GTTGGTAAAACGAAA[C/T]CTGATTAAGACTTTG | 51317 |
rs2932510 | snp | C/G | 0.167158 | 0.235875 | intron-variant | PHF21A | GRCh38.p7 | 11:46080167 | TTTATCTAACTACTA[C/G]TTTTTTTTTGAGACA | 51317 |
rs2932512 | snp | A/G | 0.168135 | 0.236216 | intron-variant | PHF21A | GRCh38.p7 | 11:46059348 | tcctgaagaataatt[A/G]agaatgtaaagaaat | 51317 |
rs2932513 | snp | A/G | 0.464096 | 0.129085 | intron-variant | PHF21A | GRCh38.p7 | 11:46048627 | ATACAAAAATTAGCC[A/G]GGCATGGTGGCATAC | 51317 |
rs2932514 | snp | A/G | 0.463881 | 0.12944 | intron-variant | PHF21A | GRCh38.p7 | 11:46048749 | CACTCCAGCTTGGGC[A/G]ACAGAGCAAGACTCC | 51317 |
rs2932515 | snp | A/G | 0.146066 | 0.227371 | intron-variant | PHF21A | GRCh38.p7 | 11:46084137 | CATTACTTAACAACA[A/G]TGTGGGAGAAGCCAA | 51317 |
rs2932516 | snp | G/T | 0.167809 | 0.236103 | intron-variant | PHF21A | GRCh38.p7 | 11:46056833 | GGAGGACAGCATGAG[G/T]ATTGTTGACTAAAAG | 51317 |
rs2932517 | snp | C/T | 0 | 0 | intron-variant, utr-variant-5-prime | PHF21A | GRCh38.p7 | 11:46075067 | TTAAAATTCCAGTTT[C/T]TGAAATGCAAACTTA | 51317 |
rs2945996 | snp | A/G | 0.204496 | 0.245824 | intron-variant | PHF21A | GRCh38.p7 | 11:45951828 | TTTTTTTTTTTTGAG[A/G]CGGAGTCTCACTCTG | 51317 |
rs2945997 | snp | A/G | 0.475789 | 0.107327 | intron-variant | PHF21A | GRCh38.p7 | 11:45955788 | GAAGCCAGCTGCCAC[A/G]TTGTGAGCAGCACTA | 51317 |
rs2945998 | snp | C/G | 0.217551 | 0.247885 | intron-variant | PHF21A | GRCh38.p7 | 11:45956066 | ccaagaattctatat[C/G]ctgcaaaactattct | 51317 |
rs2945999 | snp | G/T | 0.479014 | 0.100263 | intron-variant | PHF21A | GRCh38.p7 | 11:45961406 | GGTCACTTGGAACTA[G/T]TTTCTCTACTATTGC | 51317 |
rs2946000 | snp | A/G | 0.217551 | 0.247885 | intron-variant | PHF21A | GRCh38.p7 | 11:45961497 | AAATTTGAAGATAAT[A/G]CATTGGATAATATTA | 51317 |
rs2946001 | snp | A/G | 0.475525 | 0.107882 | intron-variant | PHF21A | GRCh38.p7 | 11:45966083 | CCTCATCCTAAATGT[A/G]AGTATTTCTTAGGAT | 51317 |
rs2946002 | snp | A/G | 0.206029 | 0.246103 | intron-variant | PHF21A | GRCh38.p7 | 11:45966344 | ATTGCCTCAGTAAGT[A/G]CCCTTTTCTTGACAA | 51317 |
rs2946003 | snp | C/T | 0.493432 | 0.0569306 | intron-variant | PHF21A | GRCh38.p7 | 11:45975963 | TCGTCCTTGCCCTCA[C/T]ACATTAAATATATGT | 51317 |
rs2946004 | snp | C/G | 0.475702 | 0.107512 | intron-variant | PHF21A | GRCh38.p7 | 11:45976254 | CCATTCATCTGACAG[C/G]GCCCTGCTCAGATGC | 51317 |
rs2946005 | snp | C/G | 0.206029 | 0.246103 | intron-variant | PHF21A | GRCh38.p7 | 11:45979678 | TGAGCTTAGTATAGT[C/G]TGAGACAGGACCCAG | 51317 |
rs2946006 | snp | A/T | 0.277867 | 0.248442 | intron-variant | PHF21A | GRCh38.p7 | 11:45983506 | TGTGAAAAAAAAAAA[A/T]TTTTAAATCAAGATT | 51317 |
rs2946008 | snp | C/G | 0.21695 | 0.247806 | intron-variant | PHF21A | GRCh38.p7 | 11:45987420 | TAATCCTGGCACTTT[C/G]GGAGGCCGAGGTGGG | 51317 |
rs2946009 | snp | A/G | 0.205723 | 0.246048 | intron-variant | PHF21A | GRCh38.p7 | 11:45993555 | TAACAAAAAGCTGGA[A/G]CTCATTTTTCTGAGC | 51317 |
rs2959082 | snp | C/G | 0.168135 | 0.236216 | intron-variant | PHF21A | GRCh38.p7 | 11:46051411 | AAACCAGAGCATTTA[C/G]CATTACCTCCCACCT | 51317 |
rs2959083 | snp | A/T | 0.166832 | 0.235761 | intron-variant | PHF21A | GRCh38.p7 | 11:46055224 | TTACCCAAATATAAC[A/T]AAGCAGCAAATTTTT | 51317 |
rs2959084 | snp | A/G | 0.484841 | 0.0857308 | intron-variant | PHF21A | GRCh38.p7 | 11:46057105 | AAACTACAATTGAGA[A/G]GTTTTTTTCCCCAAG | 51317 |
rs2959085 | snp | C/T | 0.168785 | 0.236441 | intron-variant | PHF21A | GRCh38.p7 | 11:46072810 | TCAGGCTGGGGAAAC[C/T]GAAGCTGCAACCACG | 51317 |
rs2959086 | snp | A/T | 0.462909 | 0.131034 | intron-variant | PHF21A | GRCh38.p7 | 11:46080768 | CAACTCCTGGGCTTC[A/T]GCAATCTTCCCACCT | 51317 |
rs2959087 | snp | A/C | 0.475613 | 0.107697 | intron-variant | PHF21A | GRCh38.p7 | 11:45962418 | AATGTGATACTGGAA[A/C]TGAAATATAAATAGA | 51317 |
rs2959088 | snp | C/T | 0.206029 | 0.246103 | intron-variant | PHF21A | GRCh38.p7 | 11:45963147 | TCTGGGGGCCGGGTG[C/T]GGTGGCTCACACCTG | 51317 |
rs2959089 | snp | C/T | 0.206029 | 0.246103 | intron-variant | PHF21A | GRCh38.p7 | 11:45963393 | CCATTGCACTCCAGC[C/T]TGGGTGACAAGAGTA | 51317 |
rs2959090 | snp | A/G | 0.475437 | 0.108066 | intron-variant | PHF21A | GRCh38.p7 | 11:45968388 | acttctccaacctca[A/G]ctctaactaactcta | 51317 |
rs2959091 | snp | A/G | 0.475525 | 0.107882 | intron-variant | PHF21A | GRCh38.p7 | 11:45969306 | CATGCAGAGCTGCTC[A/G]GGCCTAGGGAGAAAG | 51317 |
rs2959092 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PHF21A | GRCh38.p7 | 11:45975469 | CTAACTTCCACATCT[A/G]TTTTATATTATTTTG | 51317 |
rs2959093 | snp | A/G | 0.227664 | 0.249 | intron-variant | PHF21A | GRCh38.p7 | 11:45976634 | ATCACTTGAGCTCCG[A/G]AGTTTGAGACCAGCC | 51317 |
rs2959094 | snp | A/C | 0.21725 | 0.247846 | intron-variant | PHF21A | GRCh38.p7 | 11:45976635 | TCACTTGAGCTCCGG[A/C]GTTTGAGACCAGCCT | 51317 |
rs2959095 | snp | A/G | 0.206029 | 0.246103 | intron-variant | PHF21A | GRCh38.p7 | 11:45983212 | TGCTCCTCCCCCAGG[A/G]CCTGAAACAAAGCCG | 51317 |
rs2959096 | snp | C/G | 0.206029 | 0.246103 | intron-variant | PHF21A | GRCh38.p7 | 11:45951317 | TATCCTCGATATTAT[C/G]CTACTTTGGCCTGAA | 51317 |
rs2959097 | snp | A/T | 0.217551 | 0.247885 | intron-variant | PHF21A | GRCh38.p7 | 11:45985826 | CAATGTCTACAAAAG[A/T]AGGTCTCTTTCCTGG | 51317 |
rs2959098 | snp | C/G | 0.487995 | 0.0765403 | intron-variant | PHF21A | GRCh38.p7 | 11:45988866 | ATTGTACTTCAGCCT[C/G]GGTGACAGAGCGAGA | 51317 |
rs2959099 | snp | A/G | 0.493154 | 0.0581045 | intron-variant | PHF21A | GRCh38.p7 | 11:45992251 | CTTAGAAAATTTTTC[A/G]GCCCGGCATGGTGGC | 51317 |
rs2959100 | snp | C/G | 0.430583 | 0.172886 | intron-variant | PHF21A | GRCh38.p7 | 11:45993587 | AACTTTTCTGGGGCT[C/G]ACAGGAGGTTGGGTG | 51317 |
rs2959101 | snp | C/T | 0.427879 | 0.175668 | intron-variant | PHF21A | GRCh38.p7 | 11:45996588 | GCCAGGAATGCTACT[C/T]TCCATATGCACAAAG | 51317 |
rs2959102 | snp | C/G | 0.475789 | 0.107327 | intron-variant | PHF21A | GRCh38.p7 | 11:45954046 | TCGTTGCCCAGGCTG[C/G]AGTGCAATGGCATGA | 51317 |
rs2959103 | snp | C/T | 0.203575 | 0.245652 | intron-variant | PHF21A | GRCh38.p7 | 11:45948533 | GGAACACCTTGGCAA[C/T]GGCAGTGCTCTGTTC | 51317 |
rs2959104 | snp | A/G | 0.165527 | 0.235296 | intron-variant | PHF21A | GRCh38.p7 | 11:46043485 | TAAAGCCCATATCAC[A/G]GTCTATTAGTTATTA | 51317 |
rs3021404 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45966649 | tgtttgagatggagt[C/T]tcgctctgttgccag | 51317 |
rs3021405 | snp | C/T | 0.277778 | 0.248452 | intron-variant | PHF21A | GRCh38.p7 | 11:45971886 | GGACAGTGTCTTTTT[C/T]TTTCTTTTTTTTTTT | 51317 |
rs3061870 | in-del | -/T/TT | | | intron-variant | PHF21A | GRCh38.p7 | 11:45943139 | TCATCTTTCTTTCCT[-/T/TT]TTTTTTTTTTTTTTT | 51317 |
rs3061874 | in-del | -/CA | | | intron-variant | PHF21A | GRCh38.p7 | 11:45955307 | acacacacacacaca[-/CA]CTTTTTAATCAAAAA | 51317 |
rs3061876 | in-del | -/CT | 0.205417 | 0.245993 | intron-variant | PHF21A | GRCh38.p7 | 11:45962308 | ATACGGGTTTGGTAA[-/CT]CTGTGAACAGGTGTG | 51317 |
rs3061877 | in-del | -/AAT | | | intron-variant | PHF21A | GRCh38.p7 | 11:45978354 | AGAGATGGTAATAAT[-/AAT]AACTTCCTCTTAGGA | 51317 |
rs3061959 | in-del | -/GTT/GTTGTT/GTTGTTGTT | 0.350103 | 0.234577 | intron-variant | PHF21A | GRCh38.p7 | 11:46088408 | gttgttgttgttgtt[-/GTT/GTTGTT/GTTGTTGTT]ATTGGAAAGTTAGAG | 51317 |
rs3061961 | in-del | -/AAAAG | | | intron-variant | PHF21A | GRCh38.p7 | 11:46087553 | GAGATCTTTCTGAAG[-/AAAAG]AAAAAGAATTTCAAA | 51317 |
rs3107239 | snp | C/T | 0.206029 | 0.246103 | intron-variant | PHF21A | GRCh38.p7 | 11:45966685 | agtgcagtggcgcga[C/T]ctcggctcacagcag | 51317 |
rs3110528 | snp | C/T | 0.277778 | 0.248452 | intron-variant | PHF21A | GRCh38.p7 | 11:45971890 | AGTGTCTTTTTCTTT[C/T]TTTTTTTTTTTTTTT | 51317 |
rs3215274 | in-del | -/T | | | downstream-variant-500B, utr-variant-3-prime | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45929073 | TTGTTTATCCCTTTT[-/T]CATAATTAAAGTTTT | 51317 |
rs3220603 | microsatellite | (CA)26/27/29/32/33/34/35 | 0.67813 | 0.187375 | intron-variant | PHF21A | GRCh38.p7 | 11:46030808 | ATTGCCTACTGGAAA[(CA)26/27/29/32/33/34/35]TATGTGGTTTAGNAG | 51317 |
rs3736508 | snp | C/T | 0.211698 | 0.247049 | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45953579 | GGTGGGGTGATGGTG[C/T]GGCTCTCTGTTTGTT | 51317 |
rs3833430 | in-del | -/AG | 0.499104 | 0.0211472 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45931273 | AGGAAAAGGTAAGTT[-/AG]AGGTGTTGTGTGGCA | 51317 |
rs3929339 | snp | A/G | 0.463989 | 0.129263 | intron-variant | PHF21A | GRCh38.p7 | 11:46065176 | CCAAATGCTCAAGGA[A/G]AAAATCTCCAGCTCC | 51317 |
rs4073513 | snp | A/G | 0.485187 | 0.0847778 | intron-variant | PHF21A | GRCh38.p7 | 11:46049702 | GCCGCTGTCCTACTC[A/G]GGGGGTCCCCTCCAC | 51317 |
rs4144718 | snp | A/G | 0.475702 | 0.107512 | intron-variant | PHF21A | GRCh38.p7 | 11:46012098 | AGTCCTGAGCTGTTC[A/G]TTACTACCGGAAAGA | 51317 |
rs4237659 | snp | C/T | 0.491473 | 0.0647364 | intron-variant | PHF21A | GRCh38.p7 | 11:46011380 | TGTAATCCCAGGTAC[C/T]TAGGAGGCTGAGGCA | 51317 |
rs4237660 | snp | C/T | 0.475965 | 0.106957 | intron-variant | PHF21A | GRCh38.p7 | 11:46013915 | tgagtggttagtaaa[C/T]gtgaaagcctaacac | 51317 |
rs4237661 | snp | C/T | 0.167809 | 0.236103 | intron-variant | PHF21A | GRCh38.p7 | 11:46111815 | AAGAATTAAGATTTT[C/T]TGAAACTACACTTTC | 51317 |
rs4281461 | snp | G/T | 0.166832 | 0.235761 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46119384 | AATTCTAGAAATCCA[G/T]ACTCCCAGAGACATC | 51317 |
rs4301763 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | PHF21A | GRCh38.p7 | 11:46006170 | TTGACATAGTTCCTA[C/T]AAATAAGAGCCAAAT | 51317 |
rs4328185 | snp | C/T | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45973306 | AAGTACCTCCATTCT[C/T]TCAGAAACACATCTG | 51317 |
rs4536183 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | PHF21A | GRCh38.p7 | 11:46012591 | aaagtagctacctca[A/G]agggctgtgaagatt | 51317 |
rs4755347 | snp | A/T | 0.395453 | 0.203331 | intron-variant | PHF21A | GRCh38.p7 | 11:46037743 | GAGAAGTTTGTGGGA[A/T]TTTTCTCTTTACTTG | 51317 |
rs4756042 | snp | A/G | 0.204189 | 0.245767 | intron-variant | PHF21A | GRCh38.p7 | 11:45935927 | TATGCTAAAACTGTC[A/G]GTGGCTTGGGTCTGG | 51317 |
rs4756043 | snp | A/G | 0.214843 | 0.247516 | intron-variant | PHF21A | GRCh38.p7 | 11:45937511 | TTGAGACAGAGTCTC[A/G]CTCTTGTCACCCAGG | 51317 |
rs4756044 | snp | A/C | 0.471388 | 0.116136 | intron-variant | PHF21A | GRCh38.p7 | 11:45939563 | GCTGTTCAATGGGCC[A/C]TTCTATTCTGGGAGG | 51317 |
rs4756045 | snp | C/T | 0.470618 | 0.117591 | intron-variant | PHF21A | GRCh38.p7 | 11:45954224 | CTGGTCTTGAACTCC[C/T]GACCTCAGGTGATCC | 51317 |
rs4756048 | snp | C/T | 0.209693 | 0.246729 | intron-variant | PHF21A | GRCh38.p7 | 11:45989537 | agccgggcctgatgt[C/T]gcgcacctgtagttc | 51317 |
rs4756050 | snp | C/T | 0.475877 | 0.107142 | intron-variant | PHF21A | GRCh38.p7 | 11:46018198 | GAGCTTGCAGTGAGC[C/T]GAGATTGCGCCACTG | 51317 |
rs4756051 | snp | C/G | 0.482234 | 0.0925596 | intron-variant | PHF21A | GRCh38.p7 | 11:46034353 | TTGAATTTTTTATTG[C/G]TGTTTTTGCAATTTT | 51317 |
rs4756054 | snp | A/G | 0.462582 | 0.131564 | intron-variant | PHF21A | GRCh38.p7 | 11:46094654 | CTGGGAGGCCAAAGT[A/G]GGTGGATCACGAGAT | 51317 |
rs4756055 | snp | C/T | 0.472803 | 0.113397 | intron-variant | PHF21A | GRCh38.p7 | 11:46100472 | TTTAGAAAGGTTTTG[C/T]TGCTATAGGCGAACT | 51317 |
rs4756056 | snp | C/T | 0.167809 | 0.236103 | intron-variant | PHF21A | GRCh38.p7 | 11:46104024 | AGTTTCTAGGCTCAA[C/T]ATAGGTAGCTTATGA | 51317 |
rs4756057 | snp | C/T | 0.167809 | 0.236103 | intron-variant | PHF21A | GRCh38.p7 | 11:46111942 | TTCCAAGGTTACATA[C/T]ACTGTAACAAAAGGG | 51317 |
rs4756058 | snp | A/G | 0.16846 | 0.236329 | upstream-variant-2KB | PHF21A, LOC105376661 | GRCh38.p7 | 11:46123117 | TCCCATAGGCATGAA[A/G]TCCAGTTTTTGCAGA | 51317 |
rs5022509 | snp | C/T | 0.498611 | 0.0263212 | intron-variant | PHF21A | GRCh38.p7 | 11:45971894 | TCTTTTTCTTTCTTT[C/T]TTTTTTTTTTTATGG | 51317 |
rs5791712 | in-del | -/AC | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45955284 | GTCTTTCTCTCTCCA[-/AC]ACACACACACACACA | 51317 |
rs5791714 | in-del | -/TAA | 0.475613 | 0.107697 | intron-variant | PHF21A | GRCh38.p7 | 11:45978347 | AAAAAACAGAGATGG[-/TAA]TAATAATAACTTCCT | 51317 |
rs5791717 | in-del | -/A/AA | | | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46119122 | TTTAAAAAAAAAAAA[-/A/AA]ACTTTCATCAGCCCA | 51317 |
rs6416136 | snp | C/T | 0.167158 | 0.235875 | intron-variant | PHF21A | GRCh38.p7 | 11:46070442 | TTCAAGCAATTCTCC[C/T]GCCTCAGCCTCCTGA | 51317 |
rs6485649 | snp | A/T | 0.0387552 | 0.1337 | intron-variant | PHF21A | GRCh38.p7 | 11:45937972 | TCCAGCTCAGTAATA[A/T]GGCAGAGGGCTTCTG | 51317 |
rs6485654 | snp | A/T | 0.491104 | 0.0660973 | intron-variant | PHF21A | GRCh38.p7 | 11:46002665 | CACCTTTAAGGGATA[A/T]AATGAAGAACTTTGG | 51317 |
rs6485655 | snp | C/G | 0.348354 | 0.22984 | intron-variant | PHF21A | GRCh38.p7 | 11:46014199 | tccctagtgtttact[C/G]ttcccatctttatgt | 51317 |
rs6485660 | snp | C/T | 0.463126 | 0.13068 | intron-variant | PHF21A | GRCh38.p7 | 11:46050176 | ACATTTGCCTCCTTT[C/T]TTCCCCCCTTAATTT | 51317 |
rs6485662 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | PHF21A | GRCh38.p7 | 11:46078183 | CAAAAGGAATAAGTA[C/T]GGGCTACCAATGCCA | 51317 |
rs6485663 | snp | A/G | 0.462582 | 0.131564 | intron-variant | PHF21A | GRCh38.p7 | 11:46090025 | GGGTCCAGGCTGTCT[A/G]AATATACACATTCTT | 51317 |
rs6485664 | snp | C/T | 0.167158 | 0.235875 | intron-variant | PHF21A | GRCh38.p7 | 11:46091589 | TTAATTTTAAGAATG[C/T]AAATAAACACGAGTC | 51317 |
rs7103299 | snp | C/T | 0.167158 | 0.235875 | intron-variant | PHF21A | GRCh38.p7 | 11:46035876 | CAAATTTGCGAGCCA[C/T]GTTAAGATTTTGGAC | 51317 |
rs7106689 | snp | C/T | 0.168785 | 0.236441 | intron-variant | PHF21A | GRCh38.p7 | 11:46101102 | TACAACCATCACAGA[C/T]AGGAAAGTGTACATA | 51317 |
rs7107550 | snp | C/T | 0.498323 | 0.0289051 | intron-variant | PHF21A | GRCh38.p7 | 11:46115505 | ATAAATTCAATGCAA[C/T]GTTAACATATTATCT | 51317 |
rs7108028 | snp | A/C | 0.477004 | 0.104734 | intron-variant | PHF21A | GRCh38.p7 | 11:45943442 | acctcagcctcccaa[A/C]gtgttgggatttaca | 51317 |
rs7108186 | snp | A/C | 0.477345 | 0.103991 | intron-variant | PHF21A | GRCh38.p7 | 11:45943578 | tcttctgcatatttt[A/C]gacacagtgatcctt | 51317 |
rs7109480 | snp | C/T | 0.470424 | 0.117954 | intron-variant | PHF21A | GRCh38.p7 | 11:46114104 | ACACACACACACACA[C/T]GCACACATCCCCACA | 51317 |
rs7110825 | snp | C/T | 0.271432 | 0.24908 | intron-variant | PHF21A | GRCh38.p7 | 11:46098766 | GCATTATAAAAGAGT[C/T]TGAGCTTATTTTGGT | 51317 |
rs7111900 | snp | A/G | 0.168135 | 0.236216 | intron-variant | PHF21A | GRCh38.p7 | 11:46102886 | ACTAATAATTACAAC[A/G]GTGTTTTGTTTTTAA | 51317 |
rs7112677 | snp | A/T | 0.41141 | 0.19091 | intron-variant | PHF21A | GRCh38.p7 | 11:46090256 | ATTTAATGACTATTT[A/T]AAAAAAAACTGTCCA | 51317 |
rs7114506 | snp | A/C | 0.48498 | 0.0853497 | intron-variant | PHF21A | GRCh38.p7 | 11:46050735 | GAATGGGAATTAATA[A/C]GATTTTTAAAAATTA | 51317 |
rs7115035 | snp | G/T | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45946811 | TCCTTCTCTATTCTG[G/T]CTGCATTTTATGAGG | 51317 |
rs7117810 | snp | C/T | | | upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46121863 | TTTATTTCACTTTGC[C/T]TAAGGAACGGGGTGT | 51317 |
rs7120227 | snp | A/G | 0.167158 | 0.235875 | intron-variant | PHF21A | GRCh38.p7 | 11:46039487 | GCCCACCTTGAAGGA[A/G]GTAGCTCACCATGAT | 51317 |
rs7122062 | snp | C/G | | | upstream-variant-2KB | PHF21A, LOC105376661 | GRCh38.p7 | 11:46122749 | GCGGGGCGGGGGAGG[C/G]CCTTTTTTTTTTTTT | 51317 |
rs7125387 | snp | A/T | 0.167809 | 0.236103 | intron-variant | PHF21A | GRCh38.p7 | 11:46113975 | CAGGAAATAATTTTT[A/T]TAGTAATACGCACAC | 51317 |
rs7128184 | snp | C/T | 0.491157 | 0.065903 | intron-variant | PHF21A | GRCh38.p7 | 11:45976097 | TTATCTCCTCTCCAT[C/T]GTTTCGTGGATCACA | 51317 |
rs7129942 | snp | G/T | 0.168135 | 0.236216 | intron-variant | PHF21A | GRCh38.p7 | 11:46050272 | AGCAGCATTCCAGTG[G/T]CCTTGCTCACGGCAG | 51317 |
rs7130281 | snp | A/G | 0.485324 | 0.0843964 | intron-variant | PHF21A | GRCh38.p7 | 11:46029615 | ATCACTTGAACCCAG[A/G]AGGCAAAGGTTGCGG | 51317 |
rs7130282 | snp | C/T | 0.206336 | 0.246157 | intron-variant | PHF21A | GRCh38.p7 | 11:46029578 | ctgtaatcccagcta[C/T]ttgggaagctgaggc | 51317 |
rs7350495 | snp | A/G | 0.49334 | 0.057322 | intron-variant | PHF21A | GRCh38.p7 | 11:46002525 | AAGCACTATTTGGGG[A/G]AAAAAAAAAGGAATT | 51317 |
rs7397035 | snp | A/G | 0.167809 | 0.236103 | intron-variant | PHF21A | GRCh38.p7 | 11:46077652 | AATTTGGTTTACTCC[A/G]TGTGGACTTTTTTAT | 51317 |
rs7478883 | snp | C/G | 0.167809 | 0.236103 | intron-variant | PHF21A | GRCh38.p7 | 11:46065137 | CCTGATAACAAAAAA[C/G]AGTTTTGTTTAGGTA | 51317 |
rs7924996 | snp | C/T | 0.167484 | 0.23599 | intron-variant | PHF21A | GRCh38.p7 | 11:46096631 | tctctggctactctc[C/T]ttggtttcttttgct | 51317 |
rs7926314 | snp | G/T | 0.491104 | 0.0660973 | intron-variant | PHF21A | GRCh38.p7 | 11:46005625 | AATGAAACTATCAAC[G/T]ATCCTTTTACTAAGA | 51317 |
rs7932691 | snp | C/G | 0.455977 | 0.141681 | intron-variant | PHF21A | GRCh38.p7 | 11:46107492 | GGTAAAAAACGTTGA[C/G]TACTCTATAGTTTAA | 51317 |
rs7932895 | snp | A/G | 0.209693 | 0.246729 | intron-variant | PHF21A | GRCh38.p7 | 11:45989857 | tacaaaaattagcca[A/G]ggatggtggcataca | 51317 |
rs7934407 | snp | A/C | 0.167809 | 0.236103 | intron-variant | PHF21A | GRCh38.p7 | 11:46062192 | gtgtggggttttttt[A/C]attcacagttttagg | 51317 |
rs7934572 | snp | C/G | 0.203575 | 0.245652 | intron-variant | PHF21A | GRCh38.p7 | 11:45937097 | ATCAGGAGGAGGACA[C/G]TGAGAGAAGTGTTCC | 51317 |
rs7934681 | snp | A/G | 0.214843 | 0.247516 | intron-variant | PHF21A | GRCh38.p7 | 11:45937086 | CACAAAGCAGCATCA[A/G]GAGGAGGACACTGAG | 51317 |
rs7935282 | snp | A/T | 0.0573587 | 0.15934 | intron-variant | PHF21A | GRCh38.p7 | 11:46090659 | CCCCACCCCACCTCA[A/T]TAATACTTATTTTTT | 51317 |
rs7935308 | snp | A/T | 0.475789 | 0.107327 | intron-variant | PHF21A | GRCh38.p7 | 11:46002804 | ATCTTTATTCAAAAG[A/T]CCCTTCTTCCCCAAG | 51317 |
rs7937149 | snp | A/G | 1.654e-05 | 0.00287571 | intron-variant | PHF21A | GRCh38.p7 | 11:45950274 | TGTGCCAGAGAAACA[A/G]AAGAAGAATATGCTT | 51317 |
rs7937896 | snp | A/T | 0.463018 | 0.130857 | intron-variant | PHF21A | GRCh38.p7 | 11:46096409 | attcctctcctccca[A/T]tctctattgaacaca | 51317 |
rs7940620 | snp | A/G | 0.167809 | 0.236103 | intron-variant | PHF21A | GRCh38.p7 | 11:46109520 | ataaaaataaaattt[A/G]tatagttagtaaaat | 51317 |
rs7942083 | snp | A/G | 0.457037 | 0.140127 | intron-variant | PHF21A | GRCh38.p7 | 11:46104521 | TCTATTTTTCCCAGA[A/G]GTATTCACAAATAAG | 51317 |
rs7942246 | snp | C/T | 0.167809 | 0.236103 | intron-variant | PHF21A | GRCh38.p7 | 11:46104822 | CAGTGGTATGCAGCA[C/T]GTATGTGATACATCT | 51317 |
rs7946524 | snp | C/T | 0.16846 | 0.236329 | upstream-variant-2KB | PHF21A, LOC105376661 | GRCh38.p7 | 11:46122904 | TTAGATTAAAAAAAA[C/T]CCCTACTGGACAGTG | 51317 |
rs7947508 | snp | A/G | 0.49121 | 0.0657086 | intron-variant | PHF21A | GRCh38.p7 | 11:45998612 | ccacctcccaggttc[A/G]agtgattctcctgcc | 51317 |
rs7947815 | snp | A/G | 0.491368 | 0.0651254 | intron-variant | PHF21A | GRCh38.p7 | 11:45998614 | acctcccaggttcaa[A/G]tgattctcctgcctc | 51317 |
rs7948502 | snp | A/G | 0.491473 | 0.0647364 | intron-variant | PHF21A | GRCh38.p7 | 11:46016310 | CTCAAAATTTCCCAG[A/G]GTCTTCTCCCTAAAC | 51317 |
rs7949376 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46040935 | cacacacacacacac[A/G]cacgcacaATTAAGG | 51317 |
rs7950336 | snp | C/T | 0.493201 | 0.0579089 | intron-variant | PHF21A | GRCh38.p7 | 11:46002632 | GATATTACCATTAGA[C/T]AAAGGGGATGTCATA | 51317 |
rs7950391 | snp | C/T | 0.491629 | 0.0641526 | intron-variant | PHF21A | GRCh38.p7 | 11:46025579 | CTAAGAAAATTCCAA[C/T]TTGATTATGCTCTTA | 51317 |
rs9666859 | snp | C/T | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46091961 | TAACAGGTTATCGAA[C/T]GGTGGAACATGCAGG | 51317 |
rs10444290 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | PHF21A | GRCh38.p7 | 11:45980376 | taagtttatgaacct[A/G]cctgtgcctcactgt | 51317 |
rs10501316 | snp | C/T | 0.226188 | 0.248863 | intron-variant | PHF21A | GRCh38.p7 | 11:46068999 | TAAAATCTTTGACCA[C/T]TTAGGTACAACTAGC | 51317 |
rs10528941 | in-del | -/AATAAT/AATAATAATAAT/AATAATAATAATAAT | 0.409552 | 0.192466 | intron-variant | PHF21A | GRCh38.p7 | 11:45964200 | GAAACTCCATCTCAA[lengthTooLong]AATAATAATAATAAT | 51317 |
rs10529223 | in-del | -/AAACAC/ACACACACACACACACAC/ACACACACACACACACACAC | | | intron-variant | PHF21A | GRCh38.p7 | 11:45986084 | TATTCTTCCTTCAAA[lengthTooLong]ACACACACACACACA | 51317 |
rs10681499 | in-del | -/TT/TTT | 0.49306 | 0.0584955 | intron-variant | PHF21A | GRCh38.p7 | 11:46092759 | TTTTTTTTTTTTTTT[-/TT/TTT]GAAACAATGTCTTAC | 51317 |
rs10712240 | in-del | -/A | 0.194902 | 0.243853 | intron-variant | PHF21A | GRCh38.p7 | 11:46071734 | ATATTGATAATAGCC[-/A]AAAAAAAAAACTGGA | 51317 |
rs10717085 | in-del | -/T | 0.383246 | 0.211531 | intron-variant | PHF21A | GRCh38.p7 | 11:46112950 | TGATAAAAAATACAA[-/T]AAACTAATCTAAGGT | 51317 |
rs10718094 | in-del | -/C | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46091838 | AGCTATAGGCACACA[-/C]CCACTGGGCCTGGCT | 51317 |
rs10718095 | in-del | -/A | 0.291235 | 0.246576 | intron-variant | PHF21A | GRCh38.p7 | 11:46092095 | GAGAGCCTATTTGCC[-/A]AAAAAAAAAAAAAAT | 51317 |
rs10718245 | in-del | -/A | 0.441158 | 0.161117 | intron-variant | PHF21A | GRCh38.p7 | 11:46118418 | CAAAAGTCTGATGTT[-/A]AAAAAAAAAAAAAAA | 51317 |
rs10734539 | snp | A/G | 0.167809 | 0.236103 | intron-variant | PHF21A | GRCh38.p7 | 11:46108631 | TTTAAAAGTAGGATG[A/G]GAACGGAATGACTAA | 51317 |
rs10734540 | snp | C/T | 0.167809 | 0.236103 | intron-variant | PHF21A | GRCh38.p7 | 11:46109042 | GAAACAGCCTCAAAA[C/T]GATACACTGTAGCTG | 51317 |
rs10742773 | snp | C/T | 0.175638 | 0.238684 | intron-variant | PHF21A | GRCh38.p7 | 11:45938118 | TGGCCGTGTCTTTGT[C/T]CTCCTCGGCCCCTCC | 51317 |
rs10742774 | snp | A/C | 0.470715 | 0.117409 | intron-variant | PHF21A | GRCh38.p7 | 11:45956039 | AGTGCTGAGCAAAAA[A/C]ACCCCTATCAACCAA | 51317 |
rs10769176 | snp | C/T | 0.470811 | 0.117228 | intron-variant | PHF21A | GRCh38.p7 | 11:45961834 | GCTATATCGTAAGTC[C/T]TCTGGCTTCATCTAC | 51317 |
rs10769177 | snp | C/T | 0.206029 | 0.246103 | intron-variant | PHF21A | GRCh38.p7 | 11:45962849 | AGTGAGCCGGGATCG[C/T]GCCACTGCACTCCAG | 51317 |
rs10769178 | snp | C/G | 0.340559 | 0.233022 | intron-variant | PHF21A | GRCh38.p7 | 11:45979041 | TTTTTTTTTGAGACG[C/G]AGTTTTGCTCTGTTG | 51317 |
rs10769179 | snp | C/T | 0.491368 | 0.0651254 | intron-variant | PHF21A | GRCh38.p7 | 11:46003232 | AAAAAGTCCTAAAAA[C/T]TTTGTGCATATAGTG | 51317 |
rs10769186 | snp | C/T | 0.456685 | 0.140646 | intron-variant | PHF21A | GRCh38.p7 | 11:46105179 | TGGCAAAGCTAGGAT[C/T]TGGGCCCATGCAAAG | 51317 |
rs10838533 | snp | C/T | 0.476052 | 0.106772 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45929755 | GGTATTTTTCAGAGT[C/T]CCTACCCCGGCTTTC | 51317 |
rs10838535 | snp | C/T | 0.48978 | 0.0707512 | intron-variant | PHF21A | GRCh38.p7 | 11:45936060 | AGGCAGGTGAATCAC[C/T]TGAGCCCAGGAGTTT | 51317 |
rs10838537 | snp | A/T | 0.217551 | 0.247885 | intron-variant | PHF21A | GRCh38.p7 | 11:45973084 | ACTTCGTCTCAAAAA[A/T]AAATAAATAAATAAA | 51317 |
rs10838541 | snp | C/T | 0.471292 | 0.116318 | intron-variant | PHF21A | GRCh38.p7 | 11:46022196 | GGTGGCTCATCCCTG[C/T]AATTCCAGCACTTTG | 51317 |
rs10838542 | snp | A/G | 0.331642 | 0.236293 | intron-variant | PHF21A | GRCh38.p7 | 11:46023041 | TGGGCATGAGCCACC[A/G]CGCCCGGCCTTGTTA | 51317 |
rs10838547 | snp | C/T | 0.396909 | 0.202282 | intron-variant | PHF21A | GRCh38.p7 | 11:46038531 | TGTGATTATCTTTAT[C/T]AGTTTACTGTTGTTT | 51317 |
rs10838551 | snp | A/G | 0.395818 | 0.203069 | intron-variant | PHF21A | GRCh38.p7 | 11:46051562 | AGTACTCTAACTTTG[A/G]TCTTCAGAAACACAA | 51317 |
rs10838552 | snp | G/T | 0.396909 | 0.202282 | intron-variant | PHF21A | GRCh38.p7 | 11:46062486 | GTTTCTGTTTTCTAA[G/T]TGTTCCTTTATTTCT | 51317 |
rs10838555 | snp | C/T | 0.396546 | 0.202545 | intron-variant | PHF21A | GRCh38.p7 | 11:46070020 | AGACATATTAAGTTA[C/T]TCAATAATTAAAATC | 51317 |
rs10838558 | snp | C/G | 0.463126 | 0.13068 | intron-variant | PHF21A | GRCh38.p7 | 11:46078521 | ATCTCTTCAGAAATA[C/G]AGAATAAAATGCCTA | 51317 |
rs10838559 | snp | A/G | 0.395087 | 0.203592 | intron-variant | PHF21A | GRCh38.p7 | 11:46080970 | TGCGCAGCTCTTGCT[A/G]CTATTCTAACAACCC | 51317 |
rs10838560 | snp | A/T | 0.342134 | 0.232404 | intron-variant | PHF21A | GRCh38.p7 | 11:46086807 | CATAAACTCTGGAAA[A/T]GAACGGCAGGTTAAA | 51317 |
rs10838562 | snp | A/G | 0.383824 | 0.211166 | intron-variant | PHF21A | GRCh38.p7 | 11:46100278 | CTTGTTTAAAAAAAA[A/G]AAAATCCCATGAGCA | 51317 |
rs10838563 | snp | G/T | 0.167809 | 0.236103 | intron-variant | PHF21A | GRCh38.p7 | 11:46103269 | TTCCATTCAACCAAC[G/T]GAAACAACTTTTACA | 51317 |
rs10838564 | snp | C/G | 0.457154 | 0.139954 | intron-variant | PHF21A | GRCh38.p7 | 11:46105762 | TTTAAAAAGCACTAG[C/G]CCTCTTTGAAAGACT | 51317 |
rs10838565 | snp | A/C | 0.383632 | 0.211288 | intron-variant | PHF21A | GRCh38.p7 | 11:46109587 | TTTCATTCCCATGAC[A/C]ACACACCAGTACATT | 51317 |
rs10838566 | snp | C/T | 0.350109 | 0.229081 | intron-variant | PHF21A | GRCh38.p7 | 11:46113256 | AAAGTCTGAACTATC[C/T]AGCACAATTTGACTA | 51317 |
rs10838567 | snp | A/G | 0.383632 | 0.211288 | intron-variant | PHF21A | GRCh38.p7 | 11:46114792 | ACAATACTTGGATCT[A/G]CAGCAGAAAAAAAAT | 51317 |
rs11038716 | snp | A/G | 0.231482 | 0.249313 | intron-variant | PHF21A | GRCh38.p7 | 11:45936893 | ACCACCAACACAAAA[A/G]CTGCACATCAGCATG | 51317 |
rs11038720 | snp | A/T | 0.489024 | 0.0732638 | intron-variant | PHF21A | GRCh38.p7 | 11:45947110 | CCCATCAGCACTCCT[A/T]ACTGAGAGACCTGAT | 51317 |
rs11038721 | snp | C/T | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45950391 | AAGAGCAGGCATTCT[C/T]TAAGCAGCCATGGAG | 51317 |
rs11038723 | snp | C/T | 0.491104 | 0.0660973 | intron-variant | PHF21A | GRCh38.p7 | 11:45958341 | GCCAAGGCAGGCAGA[C/T]AGCTTGAGCTCAGGG | 51317 |
rs11038724 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45958419 | AAAAAAAAAAAAAAA[A/T]ATATATATATATATA | 51317 |
rs11038725 | snp | C/T | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45958449 | ATATATATATATATA[C/T]ACACACACACACACA | 51317 |
rs11038726 | snp | A/G | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45960813 | CGAAATTGTCTTGCA[A/G]ATGTTATTTTCTGCA | 51317 |
rs11038727 | snp | G/T | 0.375 | 0.216506 | intron-variant | PHF21A | GRCh38.p7 | 11:45962697 | AGGAGTCTGAGACCA[G/T]CCTGGCCAACATGGT | 51317 |
rs11038728 | snp | C/T | 0.375 | 0.216506 | intron-variant | PHF21A | GRCh38.p7 | 11:45962704 | TGAGACCAGCCTGGC[C/T]AACATGGTGAAACCC | 51317 |
rs11038729 | snp | C/T | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45971839 | TACAGTTCTGGATAT[C/T]TGCTTCCTGAGACAC | 51317 |
rs11038731 | snp | A/C/T | 0.0178098 | 0.0926698 | intron-variant | PHF21A | GRCh38.p7 | 11:45973750 | CCATTTAAAACATGT[A/C/T]GATTTAAAGAACTTC | 51317 |
rs11038732 | snp | G/T | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45981968 | tttttttttttttgg[G/T]tgttttgaaacaggg | 51317 |
rs11038734 | snp | A/G | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45990279 | TTTTTTTTTTTTTCA[A/G]ACAGGATCTCACTCT | 51317 |
rs11038735 | snp | C/G | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45990298 | GGATCTCACTCTGTC[C/G]CCCAGGCTGGAGTGC | 51317 |
rs11038737 | snp | A/G | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45992878 | ACCCCTGTCACATAA[A/G]ACTGACACAAGGATA | 51317 |
rs11038739 | snp | A/T | 0.259674 | 0.249813 | intron-variant | PHF21A | GRCh38.p7 | 11:45996344 | CTATATTACAATTAG[A/T]TCACATTGGTGTCTA | 51317 |
rs11038740 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45999505 | CCTTGAGACTAGAAA[G/T]TAGAATTATTCTACC | 51317 |
rs11038742 | snp | G/T | 0.230603 | 0.249246 | intron-variant | PHF21A | GRCh38.p7 | 11:46006730 | CTTGTATTAAGTATT[G/T]AACTGTCTTAAACGC | 51317 |
rs11038743 | snp | A/T | 0.259674 | 0.249813 | intron-variant | PHF21A | GRCh38.p7 | 11:46008275 | TTGTGAGGTCTTCAA[A/T]TGAAATTTTCCTGTG | 51317 |
rs11038744 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46015399 | ACTTTTGAGGACTTA[G/T]CCATAAATTCTTTGC | 51317 |
rs11038745 | snp | C/T | 0.493201 | 0.0579089 | intron-variant | PHF21A | GRCh38.p7 | 11:46026313 | TAGGGGGAAACTGCC[C/T]GAGGTGGAATATTGA | 51317 |
rs11038747 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | PHF21A | GRCh38.p7 | 11:46036689 | TTTTTTCCACTGTTA[C/T]TTCCTCACAGAGTAC | 51317 |
rs11038748 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46038241 | AAGCGATTCTCCTGC[C/G]TCAGCCTCCTGAGTA | 51317 |
rs11038749 | snp | C/G | 0.395453 | 0.203331 | intron-variant | PHF21A | GRCh38.p7 | 11:46038373 | CCTCAAGTGATCCAC[C/G]CGCCTCAGCCTCCCA | 51317 |
rs11038750 | snp | A/G | 0.0577344 | 0.159793 | intron-variant | PHF21A | GRCh38.p7 | 11:46041483 | GGAAACTAAGGGGTA[A/G]TCTGAAAGTCAGAAG | 51317 |
rs11038752 | snp | C/T | 0.226779 | 0.248919 | intron-variant | PHF21A | GRCh38.p7 | 11:46050986 | AAATATAGCAGTCTC[C/T]GAGTTCTCTGTGCCA | 51317 |
rs11038754 | snp | A/G | 0.227664 | 0.249 | intron-variant | PHF21A | GRCh38.p7 | 11:46055713 | TCTCTTTATATAAAC[A/G]CCCCAACAATTTACA | 51317 |
rs11038755 | snp | A/G | 0.030665 | 0.119967 | intron-variant | PHF21A | GRCh38.p7 | 11:46057150 | AAGGAAACTAAGAGC[A/G]GAACAGTTTTTACTG | 51317 |
rs11038756 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | PHF21A | GRCh38.p7 | 11:46057507 | AAATGTCTTGACTTA[C/T]AAAGGGAAAAACTGT | 51317 |
rs11038757 | snp | C/T | 0.0577344 | 0.159793 | intron-variant | PHF21A | GRCh38.p7 | 11:46058334 | AACTGTGTCACATTG[C/T]TGGTAAAACGAAACC | 51317 |
rs11038761 | snp | C/T | 0.343701 | 0.231776 | intron-variant | PHF21A | GRCh38.p7 | 11:46072204 | attcttactcagtaa[C/T]agtccttgaatttta | 51317 |
rs11038762 | snp | A/G | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46087028 | ACTGAAGACCTATAA[A/G]ATAATAATACTCTGA | 51317 |
rs11038763 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46087763 | GAATATTTTGAAAAA[A/T]tttttttcctgagat | 51317 |
rs11038764 | snp | A/G | 0.0554779 | 0.157039 | intron-variant | PHF21A | GRCh38.p7 | 11:46098201 | ATCTACAAAGATTTA[A/G]ACTGTACATAAATAA | 51317 |
rs11038765 | snp | C/T | 0.284733 | 0.247575 | intron-variant | PHF21A | GRCh38.p7 | 11:46101946 | CACTACAACCTCTGA[C/T]TCCTGTGTTCAAGCG | 51317 |
rs11038766 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46102021 | tgccaccacgcccag[C/T]taatttttgtatttt | 51317 |
rs11038767 | snp | C/G | 0.385168 | 0.210309 | intron-variant | PHF21A | GRCh38.p7 | 11:46105260 | AACTCCCCTTCACTC[C/G]AATTACATGAAAACA | 51317 |
rs11038768 | snp | A/G | 0.385359 | 0.210185 | intron-variant | PHF21A | GRCh38.p7 | 11:46107989 | CCAGGACTAATTCCT[A/G]TGTAGGGTATCTTTA | 51317 |
rs11038770 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | PHF21A | GRCh38.p7 | 11:46117159 | TTATATGTATTATCT[C/T]ATTTGGTCTTACTGA | 51317 |
rs11038771 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46117259 | AATTTTTAAAACTTC[A/G]ACACAAAACTTTACA | 51317 |
rs11038772 | snp | G/T | 0.388775 | 0.207946 | upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46122218 | AGCAGTTTGAAGGGG[G/T]GGGGGGAAAGCCGTG | 51317 |
rs11269016 | in-del | -/TT/TTATGATT | | | intron-variant | PHF21A | GRCh38.p7 | 11:45940658 | TCTTCCTTCATTATT[-/TT/TTATGATT]AAAATCAGGCTGAGG | 51317 |
rs11273905 | in-del | -/TGAACCCACAT | 0.463343 | 0.130326 | intron-variant | PHF21A | GRCh38.p7 | 11:46063832 | TACTGTTTCATCTGA[-/TGAACCCACAT]CATAGGATAAGCAGA | 51317 |
rs11297107 | in-del | -/T | 0.489083 | 0.0730708 | intron-variant | PHF21A | GRCh38.p7 | 11:45998834 | CTTTTTTTGTTTTTG[-/T]TTTTTTTTGAGACAG | 51317 |
rs11313984 | in-del | -/T | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46049856 | TTCCTAAAAACAACG[-/T]TAAGACTATCCAGCA | 51317 |
rs11321400 | in-del | -/T | 0.281577 | 0.247998 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46084681 | ACAACAGAATCATAA[-/T]TTTTTTTTTTTTTTT | 51317 |
rs11374563 | in-del | -/T | 0.498459 | 0.0277128 | intron-variant | PHF21A | GRCh38.p7 | 11:46109560 | AAACACAAAAGCTCA[-/T]TAATTAAAATTTTTC | 51317 |
rs11397119 | in-del | -/C | 0.172351 | 0.237636 | upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46122107 | CGGAGCCCGCGGCGG[-/C]CCCCCCCAACTCCGC | 51317 |
rs11431835 | in-del | -/C | 0.167809 | 0.236103 | intron-variant | PHF21A | GRCh38.p7 | 11:46089049 | CCATGACACAGTGTG[-/C]CCCCAAACTGTCCCT | 51317 |
rs11440493 | in-del | -/G | 0 | 0 | upstream-variant-2KB | PHF21A, LOC105376661 | GRCh38.p7 | 11:46123022 | TGGGGGGGTGGGGGG[-/G]TTTTGTTTTTAAAGC | 51317 |
rs11448208 | in-del | -/A/AA/AAA/C | 0.495855 | 0.045338 | intron-variant | PHF21A | GRCh38.p7 | 11:46067598 | CAAAAAAAAAAAAAA[-/A/AA/AAA/C]CTGAATTGAATCATT | 51317 |
rs11463148 | in-del | -/C | 0.278801 | 0.248335 | intron-variant | PHF21A | GRCh38.p7 | 11:46034222 | GCCCCCACCCCCCCC[-/C]TTGCATACTTTTCCC | 51317 |
rs11537991 | snp | C/T | 0.0141837 | 0.08301 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45932730 | AAAAAAGTTTTTTTT[C/T]CCCAGATACAAAGAT | 51317 |
rs11547493 | snp | C/T | 0.0271762 | 0.113356 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45931647 | TCTCTCTGGGCCTAA[C/T]TGGGTGGGAGAGAAG | 51317 |
rs11599960 | snp | C/G | 0.00943375 | 0.0680285 | intron-variant | PHF21A | GRCh38.p7 | 11:46044344 | TAAAAGAAGTAATTA[C/G]AAATTTGAGGGTCAG | 51317 |
rs11600077 | snp | A/G | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45974060 | TTTGTTCACATCTTA[A/G]GTTAGCAGTTTTCTT | 51317 |
rs11600515 | snp | C/G | 0.105924 | 0.204309 | intron-variant | PHF21A | GRCh38.p7 | 11:45980228 | GGAGATCACACAGCA[C/G]AGCTCAGATGTCCTA | 51317 |
rs11603659 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:45996075 | cagtctcccaagtag[C/G]tagagctacaggcat | 51317 |
rs11603846 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:45991478 | TCCATATTCCCACCT[C/G]AAACCCCCAACACCA | 51317 |
rs11604819 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46023776 | gcctcgccaacatgg[G/T]gaaaccctgtttcta | 51317 |
rs11606040 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45960836 | TTTCTGCATATATGG[G/T]GTTTAAACAGTTACC | 51317 |
rs11606041 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45960838 | TCTGCATATATGGTG[G/T]TTAAACAGTTACCAG | 51317 |
rs11820157 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | PHF21A | GRCh38.p7 | 11:46079916 | GAAAGGAAGAAAAAT[A/G]AATGTCTTTTGACCT | 51317 |
rs11820501 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | PHF21A | GRCh38.p7 | 11:45967753 | GAAAGTCTTGTCGGT[A/G]TGAATGTCTGACTGA | 51317 |
rs11820849 | snp | C/T | 0.167809 | 0.236103 | intron-variant | PHF21A | GRCh38.p7 | 11:46042086 | CACAACCATTGTCTA[C/T]AGGAAGTTGAATAAA | 51317 |
rs11820877 | snp | C/T | 0.201727 | 0.245295 | intron-variant | PHF21A | GRCh38.p7 | 11:46007322 | tttcttcttcttctt[C/T]ttttttttttcgaga | 51317 |
rs11821705 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | PHF21A | GRCh38.p7 | 11:46012134 | TCAACCAGGCCAAAG[A/G]CTCTGCCTGAAGTTC | 51317 |
rs11821943 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | PHF21A | GRCh38.p7 | 11:46027776 | TACCTGTTAAACAAT[A/G]ATTTATATCTTCTTT | 51317 |
rs11823015 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46025533 | AAAAGAAAAATTCCT[C/T]TACCTGAGAAGAAAA | 51317 |
rs11823457 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | PHF21A | GRCh38.p7 | 11:46011088 | TCTTAAAGGAGTTAC[C/T]GGACTCTTTGATCTT | 51317 |
rs11824441 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | PHF21A | GRCh38.p7 | 11:46067337 | AGTTCAATGGGGAGG[C/T]GGGCATGAGTGAGAA | 51317 |
rs11826337 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | PHF21A | GRCh38.p7 | 11:45995537 | CACTCTTGGTGCAGG[C/T]AGAGTGAGATAGAGT | 51317 |
rs11826424 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | PHF21A | GRCh38.p7 | 11:45974856 | TCTCCACAGTTTCAT[A/G]ATGGGGTCCTTTATT | 51317 |
rs11827112 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | PHF21A | GRCh38.p7 | 11:46032243 | tgtaatataatttca[C/T]ttaatttttttcaag | 51317 |
rs11827687 | snp | C/T | 0.206336 | 0.246157 | intron-variant | PHF21A | GRCh38.p7 | 11:46007133 | CCAACCATAACGTGA[C/T]GAGACATCTATCAAC | 51317 |
rs11827732 | snp | C/T | 0.167809 | 0.236103 | intron-variant | PHF21A | GRCh38.p7 | 11:46042266 | TATTCCATATTTTTA[C/T]GAATACTTGAACCAA | 51317 |
rs11828167 | snp | C/T | 0.216649 | 0.247765 | intron-variant | PHF21A | GRCh38.p7 | 11:46018046 | acgaggtcaggagat[C/T]gagaccatcccggct | 51317 |
rs12221890 | snp | A/G | 0.208474 | 0.246527 | intron-variant | PHF21A | GRCh38.p7 | 11:45962658 | GCACTTTGGGAGGCC[A/G]AGGCAGGTGGGTCGC | 51317 |
rs12224582 | snp | C/T | 0.208474 | 0.246527 | intron-variant | PHF21A | GRCh38.p7 | 11:45962657 | AGCACTTTGGGAGGC[C/T]AAGGCAGGTGGGTCG | 51317 |
rs12226174 | snp | A/C | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46001852 | GGAGGTCTTTGGTTT[A/C]TATGACAACCCAGAT | 51317 |
rs12274397 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | PHF21A | GRCh38.p7 | 11:46081729 | AGGATATACTTCATG[C/G]caaaggtaagcaaaa | 51317 |
rs12274475 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | PHF21A | GRCh38.p7 | 11:46021530 | TGCACAtgtgtgtgc[A/G]tgcatgtgtgtgtgc | 51317 |
rs12275245 | snp | A/G | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46100227 | GACCAAAAATATGTT[A/G]TGTTACAGAAGACTG | 51317 |
rs12277800 | snp | C/T | 0.491157 | 0.065903 | intron-variant | PHF21A | GRCh38.p7 | 11:46028810 | AACTCCTGACCTCAT[C/T]GTCCACTCGCCTCGG | 51317 |
rs12279644 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46089810 | TGTTTTGGAGGGGGT[G/T]GGGGGCGGGTCCTCA | 51317 |
rs12283184 | snp | C/T | 0.394721 | 0.203852 | intron-variant | PHF21A | GRCh38.p7 | 11:46091629 | AAAGTCAAGTTTCCA[C/T]AGTTAAATTAACCTA | 51317 |
rs12287443 | snp | C/T | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45939478 | ATATGCGAGTTCTTT[C/T]TAAAATGAAGAATTT | 51317 |
rs12288818 | snp | C/T | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45939523 | ACAGCTGACAATGTT[C/T]TCCTAAAACCAGTAT | 51317 |
rs12289813 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PHF21A | GRCh38.p7 | 11:45958283 | aaagccaaagacacc[A/G]aagaatagaaaaTGg | 51317 |
rs12294488 | snp | A/G | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46030613 | TTGAACACAAAATTC[A/G]AAAAGATTCTTTAAT | 51317 |
rs12294570 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46118531 | AGGATAGTTGTACAT[C/T]TACAAACGTTTTAAG | 51317 |
rs12362675 | snp | C/G | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45965145 | AACCAACTTTCTTCA[C/G]TAAGAATGACCCTTC | 51317 |
rs12363382 | snp | C/G | 0.0588605 | 0.161139 | intron-variant | PHF21A | GRCh38.p7 | 11:46091682 | GGCCATCAAATAGAA[C/G]AGCATATTAAGTAAC | 51317 |
rs12364441 | snp | C/T | 0.227664 | 0.249 | intron-variant | PHF21A | GRCh38.p7 | 11:46035522 | GAGTCCTGACTCTCA[C/T]TGAGTTTAAAACCTA | 51317 |
rs12365345 | snp | C/T | 0.274124 | 0.248833 | intron-variant | PHF21A | GRCh38.p7 | 11:46068225 | TCTCTGCATCCTCCA[C/T]GGGCCTAGTATCATG | 51317 |
rs12418498 | snp | A/G | 0.0923359 | 0.194016 | intron-variant | PHF21A | GRCh38.p7 | 11:45989296 | TTATTAAAGAGAGAG[A/G]TTCAGCATTGTAGAA | 51317 |
rs12418714 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45934593 | CCTGCAGCCTGTTTA[A/G]GCAGGTTTTGATATG | 51317 |
rs12574629 | snp | C/T | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45977815 | TATACAGTATTGGTA[C/T]TGCttttttcttttt | 51317 |
rs12574632 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | PHF21A | GRCh38.p7 | 11:45977855 | cttcttttttttttt[C/T]tGGTATTGAATGGca | 51317 |
rs12575517 | snp | G/T | 0.0482946 | 0.147699 | intron-variant | PHF21A | GRCh38.p7 | 11:46021405 | CACATTTTAAACTAT[G/T]AACAAGTATACACCA | 51317 |
rs12575764 | snp | A/G | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45935811 | TGTCCTCTGTGCTCA[A/G]AATGCCTGCCAAAGA | 51317 |
rs12575808 | snp | A/G | 0.276267 | 0.248616 | intron-variant | PHF21A | GRCh38.p7 | 11:46108676 | CGTATCTATATTGCT[A/G]GAATGACTTTCTAAC | 51317 |
rs12785662 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46022874 | tgcaacctccacctc[C/T]tgagtagctgggatt | 51317 |
rs12789745 | snp | C/G | 0.00943375 | 0.0680285 | intron-variant | PHF21A | GRCh38.p7 | 11:45955087 | TGTAATTTTCCCCCA[C/G]TGGTGTTCTCTCGTA | 51317 |
rs12791739 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46106655 | AACAAGCCAAATACA[A/C]CCACTTGTACTTAAC | 51317 |
rs12796273 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46102093 | aaactcctgaccttg[G/T]gatccacccgcctcg | 51317 |
rs12796678 | snp | A/T | 0.209997 | 0.246779 | intron-variant | PHF21A | GRCh38.p7 | 11:45962666 | ggaggccaaggcagg[A/T]gggtcgcctgaggtc | 51317 |
rs12798484 | snp | G/T | 0.277778 | 0.248452 | intron-variant | PHF21A | GRCh38.p7 | 11:45971910 | TTTTTTTTTTTATGG[G/T]GTCACCCTGGAGAGA | 51317 |
rs12799533 | snp | C/T | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46038628 | ctgagaagtccaagg[C/T]ggaggggccatatct | 51317 |
rs12801668 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | PHF21A | GRCh38.p7 | 11:46007991 | CTTGGGATTACCATG[A/C]TCCAGATAAGAACAG | 51317 |
rs12801848 | snp | A/G | 0.286521 | 0.248518 | intron-variant | PHF21A | GRCh38.p7 | 11:46102980 | AGAGACCATCAAGAG[A/G]GTAAGCAGAGAAGCA | 51317 |
rs12803224 | snp | A/C | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46002879 | ACAAAAAAACACCCA[A/C]TGTATTTAACATTAA | 51317 |
rs12803245 | snp | A/C | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46002906 | TTAAGTAGATCATTG[A/C]TACCTTTTTACTTAA | 51317 |
rs12804061 | snp | G/T | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46073477 | AAATCTTATTTCTTG[G/T]CTATTTCTGATCCTA | 51317 |
rs12807536 | snp | C/T | 0.444444 | 0.157135 | intron-variant | PHF21A | GRCh38.p7 | 11:45975377 | TAAAATAAAATAAAA[C/T]AAAACAAAACAAAAT | 51317 |
rs13377242 | snp | C/T | 0.384017 | 0.211044 | intron-variant | PHF21A | GRCh38.p7 | 11:46107289 | ATAAAAAAGGAAAAC[C/T]AGGCTCTACCACTAA | 51317 |
rs16938423 | snp | C/G | 0.0879971 | 0.190408 | intron-variant | PHF21A | GRCh38.p7 | 11:45953980 | ATAGTTGCCCAGAAG[C/G]AAGCCTGCTATTTTT | 51317 |
rs16938426 | snp | A/G | 0.0869089 | 0.189476 | intron-variant | PHF21A | GRCh38.p7 | 11:45981823 | GATTACTCATTTAAC[A/G]TATTTGAACATTAAA | 51317 |
rs16938429 | snp | G/T | 0.217551 | 0.247885 | intron-variant | PHF21A | GRCh38.p7 | 11:46000105 | TTAACTGCTTGATAG[G/T]TGTAAGCAAAATAAG | 51317 |
rs16938430 | snp | G/T | 0.0876345 | 0.190099 | intron-variant | PHF21A | GRCh38.p7 | 11:46001383 | TTCTATTCCGATAAA[G/T]TATTGCCATGTACTT | 51317 |
rs16938431 | snp | A/C | 0.0879971 | 0.190408 | intron-variant | PHF21A | GRCh38.p7 | 11:46003477 | AGTACTAATGACACT[A/C]AAACAAGAAATTGAT | 51317 |
rs16938437 | snp | C/T | 0.216649 | 0.247765 | intron-variant | PHF21A | GRCh38.p7 | 11:46031024 | AGGAGCTAGAGCCTA[C/T]ACCAGTGAGTGAACT | 51317 |
rs16938450 | snp | C/T | 0.0988009 | 0.199095 | intron-variant | PHF21A | GRCh38.p7 | 11:46076083 | ATAAACATTTACTTA[C/T]AGCTCTATCAATTGC | 51317 |
rs17725424 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | PHF21A | GRCh38.p7 | 11:46029906 | TCCCTAATTGGTAGG[C/T]AAAATACTTTAATAC | 51317 |
rs17725532 | snp | C/T | 0.226779 | 0.248919 | intron-variant | PHF21A | GRCh38.p7 | 11:46073622 | TTGCATACGTTTACA[C/T]GCCCACATACATATA | 51317 |
rs17787304 | snp | A/G | 0.0941369 | 0.195465 | intron-variant | PHF21A | GRCh38.p7 | 11:46000155 | CAAATTGTTAGTGAA[A/G]GCAGCAAACTATAGA | 51317 |
rs17787346 | snp | C/T | 0.095934 | 0.196885 | intron-variant | PHF21A | GRCh38.p7 | 11:46011553 | TGGCAATTTCTAAGA[C/T]ACTTTCTCGCTCTGG | 51317 |
rs17787417 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | PHF21A | GRCh38.p7 | 11:46067277 | GTTGAAGAAACGACA[C/G]AGCATAACAAGTATC | 51317 |
rs17789460 | snp | C/T | 0.040671 | 0.13668 | intron-variant | PHF21A | GRCh38.p7 | 11:45950402 | TTCTCTAAGCAGCCA[C/T]GGAGATCCTCTACAG | 51317 |
rs17789551 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | PHF21A | GRCh38.p7 | 11:46025239 | GAGTATGATTTCATA[C/T]CACAGATACAAAGAG | 51317 |
rs17789617 | snp | C/T | 0.101658 | 0.201233 | intron-variant | PHF21A | GRCh38.p7 | 11:46069191 | CTGAATATAAGCCAA[C/T]AGGATTTCACCAGGA | 51317 |
rs28494611 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45978333 | AAAACAAACAAACAA[A/C]AAAACAGAGATGGTA | 51317 |
rs33930558 | in-del | -/TG | | | intron-variant | PHF21A | GRCh38.p7 | 11:45940659 | CTTCCTTCATTATTA[-/TG]AAATCAGGCTGAGGG | 51317 |
rs33935532 | in-del | -/A/AA | 0 | 0 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46119123 | TTTAAAAAAAAAAAA[-/A/AA]CTTTCATCAGCCCAA | 51317 |
rs33984397 | in-del | -/CT | | | intron-variant | PHF21A | GRCh38.p7 | 11:45962309 | TACGGGTTTGGTAAC[-/CT]TGTGAACAGGTGTGA | 51317 |
rs34014401 | snp | G/T | 0.125182 | 0.216612 | intron-variant | PHF21A | GRCh38.p7 | 11:45998839 | TTTGTTTTTGTTTTT[G/T]TTTGAGACAGTCTCA | 51317 |
rs34034031 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46049078 | AGGGATGACAATGCT[-/G]TCACACCAAGTTTTA | 51317 |
rs34072905 | in-del | -/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46114282 | ATTTACATATATACA[-/C]GTTGCTACACACCCT | 51317 |
rs34081431 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46055775 | ATAAGTTACATAGCA[-/G]GGGGATTCATTGAAA | 51317 |
rs34091466 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | PHF21A | GRCh38.p7 | 11:46065412 | CAGCCATCCCATGAC[A/T]ACAGCAGTGGTTGCC | 51317 |
rs34104128 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46066745 | ATAAATTTAAATAAC[-/A]AAAGCATATATAAAG | 51317 |
rs34117276 | in-del | -/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45939969 | ATTCTGCCAGAAGGT[-/C]CTAATACAGAAATTG | 51317 |
rs34130411 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46079845 | GGAAAGGAAAGGAAA[-/G]GGAAAGAGGAAAGGA | 51317 |
rs34135200 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46116610 | CTAGGCAGCATTTTT[-/T]CAAAAGCAGCTTCAA | 51317 |
rs34199954 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46034838 | CTACAAGGGGATAGT[-/G]GGGCATGTGACCCTG | 51317 |
rs34200870 | in-del | -/T | 0.269538 | 0.249235 | intron-variant | PHF21A | GRCh38.p7 | 11:46096389 | GGTAACCATACTCCC[-/T]TCTAATTCCTCTCCT | 51317 |
rs34203313 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45973989 | AAGCCTCAAACTCAC[C/T]TGAATTATATACTTA | 51317 |
rs34225581 | snp | A/T | 0.0444908 | 0.142359 | intron-variant | PHF21A | GRCh38.p7 | 11:46076044 | GGGGAAGAAACAAGA[A/T]AACAAATGCTTTGTG | 51317 |
rs34311107 | in-del | -/AG | | | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45931274 | GGAAAAGGTAAGTTA[-/AG]GGTGTTGTGTGGCAA | 51317 |
rs34312343 | in-del | -/T | 0.463774 | 0.129618 | intron-variant | PHF21A | GRCh38.p7 | 11:46079429 | ACGGGTGACAGTGGC[-/T]TCCGAAAGGAATTTA | 51317 |
rs34326686 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46026269 | CCAGCTCAGTGGCAT[-/G]GGGATATGTTTTGTA | 51317 |
rs34330715 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46087487 | AAAACTAAAAGGGTT[-/A]AAAAAGTTAGGACTA | 51317 |
rs34340977 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46089185 | ATTTTTTTAAATAGG[-/A]AAAAGTAGGTCTTGA | 51317 |
rs34359468 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45937474 | GTGAAATGGGTGTTG[G/T]TTTATTATTAGTATT | 51317 |
rs34387228 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46079669 | AAGGAGTTCGGTGCA[-/G]GGGGAGGATAAGTTC | 51317 |
rs34390266 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46114284 | TTACATATATACAGT[-/G]TGCTACACACCCTCC | 51317 |
rs34396514 | snp | C/T | 0.275197 | 0.248727 | intron-variant | PHF21A | GRCh38.p7 | 11:46109162 | TTAAGAGCAAGGGCT[C/T]AGGAATCAAACCTGG | 51317 |
rs34398600 | in-del | -/A | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46113825 | GTGAGATTCATTCTC[-/A]AAAAAAAAAAAAAAA | 51317 |
rs34408080 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46103895 | AGAGACATTCGTAAG[A/C]CAGATACATATATAC | 51317 |
rs34414772 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45958491 | ATTAGCCAGGCATGG[G/T]GGTGCGCAACTGTAG | 51317 |
rs34512086 | in-del | -/A | 0.217551 | 0.247885 | intron-variant | PHF21A | GRCh38.p7 | 11:45957223 | CTTTAAGTAATGGAT[-/A]AAACTTGTGCAGAGA | 51317 |
rs34518435 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46101768 | GCCTCCCTAATAGCT[-/G]GGGACTACAGGCACA | 51317 |
rs34521543 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46102536 | CACAACACCAAAATT[-/G]TCCATTTTTTAATTC | 51317 |
rs34524197 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46088628 | GTAAATCAGGAAAAT[-/G]GGAAACAATATCACC | 51317 |
rs34542858 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46101802 | ACCACACTCGGCTAA[-/T]TTTTTGTATTTTTTG | 51317 |
rs34575098 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45958107 | TAACAACTAGTGACT[-/G]GAAACAGTAATCAAA | 51317 |
rs34578435 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46114131 | CACACACACACGCTT[C/T]TACAAAGAACACTTA | 51317 |
rs34584408 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46094733 | GTAGAAGTCTCTACT[-/A]AAAATACAAAAAAAA | 51317 |
rs34594042 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46021292 | TCTTGAACTCGTGGT[-/A]CTCAAGCGATCCTCC | 51317 |
rs34627524 | in-del | -/AGATAGTCATA | 0.394904 | 0.203722 | intron-variant | PHF21A | GRCh38.p7 | 11:46069511 | GGTATTAGAGGCTGG[-/AGATAGTCATA]TATCAGGTAACCAAC | 51317 |
rs34654657 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46039568 | TTTTATCTTAAACCT[-/G]GGAGTTCTATACCCT | 51317 |
rs34676719 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45977289 | TTACAGGTATATGTT[A/G]CCACGCATGGCTAAT | 51317 |
rs34783197 | snp | G/T | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45987791 | GTCCCTCTGTAACTG[G/T]CTGTTTACAGAACAC | 51317 |
rs34814729 | in-del | -/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45994870 | ACGCTTTGAATGTCT[-/C]CCCTGGTATTTCTCT | 51317 |
rs34907534 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:45953665 | TTCAGAATTCGTTTT[-/A]TTATTAAAAGGATGA | 51317 |
rs34930870 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46044955 | TCTAGTTCTAGGCAA[-/G]GGATAGTATGGTCAT | 51317 |
rs34978138 | snp | A/G | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45979982 | CTACCAAATGAAGAC[A/G]AAAAGAAATAAAAGA | 51317 |
rs35019886 | in-del | -/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46104192 | GCCACTTTTATATCT[-/C]CTGGGGTTCTACAAT | 51317 |
rs35024202 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46049093 | TCACACCAAGTTTTA[-/G]GAAAGGAGAGATTAT | 51317 |
rs35092339 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46066133 | AGAAAAAAGTAGGCT[-/G]CTATTTTATTTGATA | 51317 |
rs35117051 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46020494 | GATTACTGCTGTATC[-/T]TTTAAAGCAGGCCCT | 51317 |
rs35128677 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930631 | TTACCAGGATGCAGC[-/T]GCCTGGACAGGAGCT | 51317 |
rs35141999 | in-del | -/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45994852 | AGTTTGTCTAGTCAT[-/C]CACACGCTTTGAATG | 51317 |
rs35144908 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46074458 | AGTGGCTCTTTTGGC[-/G]GGGGGGGGGGAAGGC | 51317 |
rs35170501 | snp | A/G | 5.2975e-05 | 0.00514633 | synonymous-codon, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45933998 | CCAGAGCTGCACAGC[A/G]AACTGTAACCAGGGG | 51317 |
rs35171242 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:45950971 | ATCACACATGAACCT[-/A]AAAATTATGGAGCAA | 51317 |
rs35182637 | in-del | -/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46100957 | AACAAGCATTCCTTA[-/C]ACCAATACACACATT | 51317 |
rs35185453 | in-del | -/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46114239 | ATCAGTAACACGTCC[-/C]AAACACAAGCTGATA | 51317 |
rs35270965 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45950964 | TTTTCAATCACACAT[-/G]GAACCTAAAAATTAT | 51317 |
rs35282408 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46049359 | TATGCCCTCACCATT[-/G]CCTTTTGATCCATTA | 51317 |
rs35282698 | in-del | -/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46011234 | GGCTCACACCTGTAA[-/C]CCCCAGCACTTTGGG | 51317 |
rs35299507 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:45948047 | TGTGTGTGCACATGC[-/A]AAAATTAGTATGCTA | 51317 |
rs35323279 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:45991516 | CTTGCTGGTAAGGAT[-/A]CTGGAGCCCTCACAC | 51317 |
rs35387940 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46088058 | CACTGCACCCAGCTG[-/A]AAAAATATTTTGAGG | 51317 |
rs35389845 | in-del | -/A | 0.498206 | 0.0298983 | intron-variant | PHF21A | GRCh38.p7 | 11:45963438 | AAAAAAAAAAAAAAA[-/A]GAAAAGAAAAAAAAA | 51317 |
rs35429504 | snp | A/G | 0.000115533 | 0.00759957 | missense, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45938285 | GAGGATTTTTGCAGC[A/G]TTTGCAGAAAAAGTG | 51317 |
rs35434803 | in-del | -/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45979401 | TAGTTGCTAAGAATT[-/C]CCAGAAGAGGTCAAG | 51317 |
rs35451409 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46098917 | CTAACTGTAACTACT[-/G]GGGAGTTGTTCGCTC | 51317 |
rs35496364 | in-del | -/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46083989 | GGAATACTTTAAGTT[-/C]CTTAAAAGCAGTATC | 51317 |
rs35525494 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46014979 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 51317 |
rs35528009 | in-del | -/TG | | | intron-variant | PHF21A | GRCh38.p7 | 11:46021546 | GCATGTGTGTGTGCA[-/TG]TGTGTGTGTGTGTTC | 51317 |
rs35540561 | in-del | -/T/TT/TTT | 0.47852 | 0.101384 | intron-variant | PHF21A | GRCh38.p7 | 11:45943121 | ATCATCTTTCTTTCC[-/T/TT/TTT]TTTTTTTTTTTTTTT | 51317 |
rs35566040 | in-del | -/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46093161 | TTTAGGTTTTGGGAT[-/C]CCCAATCCAATATTA | 51317 |
rs35580116 | in-del | -/ATCT/ATCTATCT/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46015895 | TGCTGTTTTACAGTC[-/ATCT/ATCTATCT/T]ATCTATCTATCTATC | 51317 |
rs35588803 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45932936 | AAGAAAGTAAAATGA[A/C]CAGTAAAATAAAACT | 51317 |
rs35619870 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46057510 | GTCTTGACTTATAAA[-/G]GGGAAAAACTGTACT | 51317 |
rs35646259 | snp | C/T | 0.00372979 | 0.0430231 | synonymous-codon, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45965429 | TGGGCAGACTGCAAC[C/T]ATAGCCAAAACGTTC | 51317 |
rs35673374 | in-del | -/ACAC | 0.49925 | 0.0193563 | intron-variant | PHF21A | GRCh38.p7 | 11:46040891 | TACACTGACAGGAAG[-/ACAC]ACACACACACACACA | 51317 |
rs35677534 | in-del | -/T | 0.489434 | 0.0719116 | intron-variant | PHF21A | GRCh38.p7 | 11:45974620 | TGGCTAATTTTTTTT[-/T]ATTTTTAGTAGAGAC | 51317 |
rs35689706 | in-del | -/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46030642 | TCCTAAAACACATAT[-/C]TTGTATCTTTTAAAC | 51317 |
rs35736241 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45942161 | GCTGAGTTTAACTTA[-/G]GGGAGTTCTTTAGAA | 51317 |
rs35762398 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45954129 | GCCTCCCTAGTACCT[-/G]GGGATTACAGGCACC | 51317 |
rs35795644 | in-del | -/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46070314 | TTATATTGAAAAGAT[-/C]CTGTAAGAAATGGTG | 51317 |
rs35832560 | in-del | -/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46053977 | GCAGCATCCACGATT[-/C]CCATTTGGACCTTTC | 51317 |
rs35843112 | in-del | -/A | 0.482534 | 0.0918038 | intron-variant | PHF21A | GRCh38.p7 | 11:46043633 | GCCAAAAGGGCCATT[-/A]AAAAAAAAAACTGAC | 51317 |
rs35879190 | in-del | -/T | 0.205723 | 0.246048 | intron-variant | PHF21A | GRCh38.p7 | 11:45997577 | CTCTGCCTAATAACA[-/T]TTTTCATTTCCCAAT | 51317 |
rs35944820 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45989063 | CCTCGTCAAACAACA[-/G]GGGAGGGTGCAAGTT | 51317 |
rs35947423 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45947432 | ACAAGAGTCATGATT[-/G]CTGTCAGATGTTACA | 51317 |
rs35961635 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46057522 | AAAGGGAAAAACTGT[-/G]ACTTTCTGTTCTCCA | 51317 |
rs35966750 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46005681 | GTTAAATAAACATTA[-/G]GGGGAACCATCAGCA | 51317 |
rs35979662 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:45950714 | GACAGAAATCAGTAT[-/A]CTTGTGTGATCCGAG | 51317 |
rs35981714 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46118554 | GTTTTAAGTACAGAA[-/A]TTTTTTTATAAACAT | 51317 |
rs35982936 | in-del | -/T/TT | 0.304438 | 0.244001 | intron-variant | PHF21A | GRCh38.p7 | 11:45990712 | CAGTCCCTTGATTTG[-/T/TT]TTTTTTTTTTTTAAA | 51317 |
rs35995547 | in-del | -/A | 0.497182 | 0.037434 | intron-variant | PHF21A | GRCh38.p7 | 11:45935764 | AAAAAAAAAAAAAAA[-/A]GGAACGGTTTTTGAC | 51317 |
rs36029575 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45995561 | TAGAGTGGTTGAGCA[-/G]GTTCATTTTTCTTTA | 51317 |
rs36039206 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:46076228 | TGCCCTATATAGAAT[-/A]AAGTCTAATAACATT | 51317 |
rs36094505 | snp | A/C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45972100 | AATCTTTTCTCTGGA[A/C/G]AACTGCTGCAGAAGT | 51317 |
rs36095981 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46027226 | ACTGATTTCTACAAG[-/T]TTTTCTCCGTGCTAA | 51317 |
rs36099003 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46004400 | ACCAAAGGAAATGGA[-/T]TTTCACTTTTAATAG | 51317 |
rs36102025 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:45983495 | CTGTTGCTATCTGTG[-/A]AAAAAAAAAAATTTT | 51317 |
rs55722202 | snp | C/G | | | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46119889 | CGCCCCTCCCCCCGG[C/G]GGGGGCGCGGGCGGG | 51317 |
rs55768306 | in-del | -/CAAAA | | | intron-variant | PHF21A | GRCh38.p7 | 11:45975391 | TAAAACAAAACAAAA[-/CAAAA]TAAAATAAAACAGAT | 51317 |
rs55789907 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45983038 | GCCCAGAACCCATTT[C/T]CAATGTCATGTACAA | 51317 |
rs55803326 | in-del | -/AC/ACACACAC | | | intron-variant | PHF21A | GRCh38.p7 | 11:46099563 | CACACACACACACAC[-/AC/ACACACAC]CCTAAACACAAACAC | 51317 |
rs55807832 | in-del | -/AA | | | intron-variant | PHF21A | GRCh38.p7 | 11:45949222 | GAAACTTAGGAAAAA[-/AA]CCTAAGGGGTAAGCA | 51317 |
rs55868647 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46030842 | GTGCGTGTGTGTGTG[C/T]GTGTGTGTGTGTGTG | 51317 |
rs55879730 | snp | A/C/T | 0.00676944 | 0.0578265 | intron-variant | PHF21A | GRCh38.p7 | 11:46020447 | AGCACCGTGTACATA[A/C/T]GCAGCGGATGGAAGT | 51317 |
rs55897128 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46008677 | ACTCTCTGAGTTCCA[A/G]TATATTCATTTATAA | 51317 |
rs55969426 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45978924 | ACCTGTAGCTTTCAT[G/T]TCAGATTCCCATCAG | 51317 |
rs56119409 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46001205 | AAAAACTTAAAGCCA[C/T]GTATGGTTCTGGTAG | 51317 |
rs56135822 | in-del | -/A/T | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45990724 | TTGTTTTTTTTTTTT[-/A/T]AAAGAAGACTTTATT | 51317 |
rs56375192 | in-del | -/TATACACACACACA/TATATACACACACA | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45958450 | ATATATATATATATA[lengthTooLong]CACACACACACACAC | 51317 |
rs56407602 | in-del | -/CTAT/CTATCTAT | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46015937 | TATCTATCTATCTAT[-/CTAT/CTATCTAT]GCAGAAGGAGTATAT | 51317 |
rs56852527 | snp | C/T | 0.260504 | 0.249779 | intron-variant | PHF21A | GRCh38.p7 | 11:46026833 | GCAGAGCCAGCATCA[C/T]GAAGAATGCTGAGAA | 51317 |
rs56931455 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:45939795 | AAAAAAAAAAAAAAA[-/A]GAGCTATTAAAGAGG | 51317 |
rs57081937 | in-del | -/C/CTTTTTTTTTTTTTTTTTTTTT/CTTTTTTTTTTTTTTTTTTTTTTT | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45971893 | TCTTTTTCTTTCTTT[lengthTooLong]TTTTTTTTTTTTATG | 51317 |
rs57129803 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PHF21A | GRCh38.p7 | 11:45938784 | TGCAGTTGACTATGC[A/G]TAACTGAAACAATAA | 51317 |
rs57199754 | snp | C/T | 0.0876345 | 0.190099 | intron-variant | PHF21A | GRCh38.p7 | 11:45943854 | ATGCCCTGATAATGA[C/T]CCATCGTCACTTATT | 51317 |
rs57202935 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | PHF21A | GRCh38.p7 | 11:45940690 | CTACTCTTTTCCTCT[A/G]GAGGGTCAGCCTTTC | 51317 |
rs57321515 | snp | A/G | 0.0667028 | 0.170006 | intron-variant | PHF21A | GRCh38.p7 | 11:46091975 | ACGGTGGAACATGCA[A/G]GCCTAGCTGTATTAG | 51317 |
rs57370032 | in-del | -/AA | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45989510 | AAAAAAAAAAAAAAA[-/AA]TACAAAAAATTAGCC | 51317 |
rs57387891 | in-del | -/AC | | | intron-variant | PHF21A | GRCh38.p7 | 11:46114086 | CACACACACACACAC[-/AC]GCACACATCCCCACA | 51317 |
rs57431270 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | PHF21A | GRCh38.p7 | 11:45961071 | AATTAAGAATAAAAG[C/T]GGGATATCTGTTATA | 51317 |
rs57573859 | in-del | -/TGT/TGTA/TGTATGTATGTATGTA | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45987284 | GTATGTATGTATGTA[-/TGT/TGTA/TGTATGTATGTATGTA]ACCTGACCCATCAAA | 51317 |
rs57660258 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | PHF21A | GRCh38.p7 | 11:46022819 | ACGGAGTCTCGGTCT[A/G]TTACCCAGGCTGGAG | 51317 |
rs57904329 | in-del | -/C | 0.16846 | 0.236329 | intron-variant | PHF21A | GRCh38.p7 | 11:46110569 | TATTTTCTATATTGG[-/C]CCATTAACACCAGGG | 51317 |
rs58263597 | in-del | -/T | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45951808 | TTTTTTTTTTTTTTT[-/T]GAGACGGAGTCTCAC | 51317 |
rs58370310 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | PHF21A | GRCh38.p7 | 11:45941507 | AAAATGGCAAATGAT[C/G]GTTTAGTATCATTAT | 51317 |
rs58460605 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46016984 | GGATTTTTTTTTTTT[-/T]AATTGAGATGGAGTC | 51317 |
rs58576083 | in-del | -/TAAAA | | | intron-variant | PHF21A | GRCh38.p7 | 11:45975377 | TAAAATAAAATAAAA[-/TAAAA]CAAAACAAAATAAAA | 51317 |
rs58644528 | in-del | -/AATAATAATAAT/AATAATAATAATAAT/TAA | 0.625 | 0.125 | intron-variant | PHF21A | GRCh38.p7 | 11:45964236 | AATAATAATAATAAT[lengthTooLong]TTATTTCTGAATGTT | 51317 |
rs58858576 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46063998 | CACATACTCAGAAAA[A/C]CAAATTTCAAGTTCT | 51317 |
rs59130252 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46046044 | TTCAGAAATGCAATT[C/T]TCAGCTTTGTGAGCT | 51317 |
rs59345521 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | PHF21A | GRCh38.p7 | 11:46036089 | CTTATGGAAAGAAGA[C/T]AGATTTAAAAAGATA | 51317 |
rs59470131 | in-del | -/TT | 0.206029 | 0.246103 | intron-variant | PHF21A | GRCh38.p7 | 11:45966195 | CTATGTACTGAAGAC[-/TT]TCACACTTTTACCTC | 51317 |
rs59494994 | in-del | -/AC | | | intron-variant | PHF21A | GRCh38.p7 | 11:46040934 | CACACACACACACAC[-/AC]GCACGCACAATTAAG | 51317 |
rs59583388 | in-del | -/AAAAAAAAAA | | | intron-variant | PHF21A | GRCh38.p7 | 11:45968948 | AAAAAAAAAAAAAAA[-/AAAAAAAAAA]TAGGCAGGTATCCCT | 51317 |
rs59660110 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45975372 | TAAAATAAAATAAAA[C/T]AAAATAAAACAAAAC | 51317 |
rs59671545 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46004078 | TTGGTTTTTTTAAAC[A/G]GAGTCACAAAGTAGA | 51317 |
rs59768591 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46060532 | CTAAGTAAATTCTAA[C/T]CACTCATTGTGGTTC | 51317 |
rs59789351 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | PHF21A | GRCh38.p7 | 11:46094849 | AGACTGCAGTGAACT[A/G]AGATCGCGCCACTAC | 51317 |
rs59807950 | in-del | -/ATTATT | 0.375 | 0.216506 | intron-variant | PHF21A | GRCh38.p7 | 11:45974419 | GGTGTCAAACGACAA[-/ATTATT]ATTATTATTATTATT | 51317 |
rs59831481 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46030094 | TATTCATTACGGTCT[C/T]TGGACAAAGAATCAA | 51317 |
rs59866051 | in-del | -/AAAAAAAAAAA | 0.440609 | 0.161766 | intron-variant | PHF21A | GRCh38.p7 | 11:45981393 | GTGAAACCCTGTCTC[-/AAAAAAAAAAA]AAAAAAAAAAAAAAA | 51317 |
rs59967985 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45958447 | ATATATATATATATA[C/T]ATACACACACACACA | 51317 |
rs60087987 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | PHF21A | GRCh38.p7 | 11:45978258 | GTGAGCCAAGACTGC[A/G]CCACTGCACTCCAGC | 51317 |
rs60179976 | in-del | -/CACACACACACACACACA/CACACACACACACACACACA | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45986109 | ACACACACACACACA[lengthTooLong]GAGGTATTTACATCA | 51317 |
rs60195978 | in-del | -/CAA/CAACAA | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46088437 | CAACAACAACAACAA[-/CAA/CAACAA]AACATAAAAACCAAA | 51317 |
rs60341823 | in-del | -/ACACACAC | | | intron-variant | PHF21A | GRCh38.p7 | 11:46040927 | CACACACACACACAC[-/ACACACAC]GCACGCACAATTAAG | 51317 |
rs60482935 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46003299 | AAAAAAAAAAAAAAA[G/T]GCCAAGTTTTCTTTT | 51317 |
rs60558267 | in-del | -/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46074468 | TTGGCGGGAGGGGGG[-/G]AAGGCATATAGCATT | 51317 |
rs60602723 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46037479 | AAACCCCGTCTCTAC[A/T]AAAAATAAAAAATTA | 51317 |
rs60623533 | snp | A/C | 0.0995161 | 0.199636 | intron-variant | PHF21A | GRCh38.p7 | 11:46063131 | GAGACGAAGAGAATA[A/C]AAAATAAAAGTGGCT | 51317 |
rs60775450 | in-del | -/CA | | | intron-variant | PHF21A | GRCh38.p7 | 11:45958470 | ACACACACACACACA[-/CA]TATATATTAGCCAGG | 51317 |
rs60788619 | in-del | -/CTCTCTCT | | | utr-variant-5-prime, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46121203 | TCTCTCTCTCTCTCT[-/CTCTCTCT]GGGCTGTTTCTTTCC | 51317 |
rs60856235 | in-del | -/A/AA | 0.385932 | 0.209815 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46119744 | GAAAAAAAAAAAAAA[-/A/AA]GAAATCCTAACAGCA | 51317 |
rs60927389 | in-del | -/A | 0.349452 | 0.229367 | intron-variant | PHF21A | GRCh38.p7 | 11:45950528 | TTCAAAAAAAAAAAA[-/A]TCGCAAAAAAAACTC | 51317 |
rs60985678 | in-del | -/CGTGTGTGTG | | | intron-variant | PHF21A | GRCh38.p7 | 11:46030830 | GTGTGCGTGTGTGTG[-/CGTGTGTGTG]TGTGTGTGTGTGTGT | 51317 |
rs60992694 | in-del | -/AC | | | intron-variant | PHF21A | GRCh38.p7 | 11:46040933 | CACACACACACACAC[-/AC]GCACGCACAATTAAG | 51317 |
rs61058731 | in-del | -/A | | | intron-variant | PHF21A | GRCh38.p7 | 11:45957769 | AAAAAAAAAAAAAAA[-/A]GAAAAAAGAAAATAA | 51317 |
rs61091054 | in-del | -/T/TA/TATATA/TATATATATA | | | intron-variant | PHF21A | GRCh38.p7 | 11:46108587 | ATATATATATATATA[-/T/TA/TATATA/TATATATATA]AAATACATATGTAAA | 51317 |
rs61166313 | in-del | -/TTTT | | | intron-variant | PHF21A | GRCh38.p7 | 11:45940660 | TTCCTTCATTATTAA[-/TTTT]AATCAGGCTGAGGGC | 51317 |
rs61283697 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46003298 | CAAAAAAAAAAAAAA[A/T]TGCCAAGTTTTCTTT | 51317 |
rs61505607 | in-del | -/C | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930906 | ACAGGCCCCCCCCCC[-/C]TCCCCGCCCAGGTCT | 51317 |
rs61515310 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46117909 | TATGAATGGAATTTT[A/T]AAATGGACTTACTCA | 51317 |
rs61647770 | snp | C/T | 0.039522 | 0.134904 | intron-variant | PHF21A | GRCh38.p7 | 11:46023991 | AATCACTGAATGGCA[C/T]AGAGCATGTAGCAAC | 51317 |
rs61652532 | snp | C/T | 0.222928 | 0.24853 | intron-variant | PHF21A | GRCh38.p7 | 11:46011420 | CCTGAGCCCAGTAGG[C/T]GGAGGTTGCAGCAGT | 51317 |
rs61882483 | snp | A/G | 0.0189856 | 0.0955633 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930192 | AGGGAGGCTCTGATG[A/G]CCCCAAGAGAGAAGT | 51317 |
rs61882500 | snp | A/G | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45955565 | AAGCAATTAGCAGCA[A/G]TGCTTTTAAGGAAGG | 51317 |
rs61882501 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | PHF21A | GRCh38.p7 | 11:45960798 | ACCATGATGCAGACT[C/T]GAAATTGTCTTGCAG | 51317 |
rs61882502 | snp | A/T | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45970314 | TCCTATAGAAAATTT[A/T]CTAACTCTCAGTATC | 51317 |
rs61882503 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | PHF21A | GRCh38.p7 | 11:45984253 | TCTTTTCTTCTTAAT[A/G]TATTTCTATAAACAA | 51317 |
rs61882505 | snp | G/T | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45987078 | ATGCGTAAAAGAGAT[G/T]CCCAATTTAAATGTA | 51317 |
rs61882506 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | PHF21A | GRCh38.p7 | 11:45991799 | TGAATGGCAAGAATA[C/G]ATTCCTGATGTATAT | 51317 |
rs61882507 | snp | C/T | 0.178465 | 0.239547 | intron-variant | PHF21A | GRCh38.p7 | 11:45997088 | TGAAAATTAATAAGA[C/T]GCTTAGTATTTCTGA | 51317 |
rs61882508 | snp | A/G | 0.206642 | 0.246211 | intron-variant | PHF21A | GRCh38.p7 | 11:45998587 | GCGTGATCTTGGCTC[A/G]GCGCAACCTCCACCT | 51317 |
rs61882509 | snp | C/T | 0.216649 | 0.247765 | intron-variant | PHF21A | GRCh38.p7 | 11:46000519 | TTAAAGACTCTATAA[C/T]GTTTTTCTTTTGAAA | 51317 |
rs61882510 | snp | A/G | 0.205723 | 0.246048 | intron-variant | PHF21A | GRCh38.p7 | 11:46001602 | AAAAGAACAGGAAAA[A/G]GATTAACTACATTCT | 51317 |
rs61882511 | snp | C/T | 0.205723 | 0.246048 | intron-variant | PHF21A | GRCh38.p7 | 11:46004784 | TCATCATCTAAAAGA[C/T]GTCTTTGTAAAATAC | 51317 |
rs61882513 | snp | C/T | 0.205723 | 0.246048 | intron-variant | PHF21A | GRCh38.p7 | 11:46011537 | GTTGAAGTAAGAAGA[C/T]TGGCAATTTCTAAGA | 51317 |
rs61882514 | snp | A/C | 0.21725 | 0.247846 | intron-variant | PHF21A | GRCh38.p7 | 11:46013469 | ATATTTTTGGGCCTC[A/C]GCTGACCGTGAGTAA | 51317 |
rs61882534 | snp | A/G | 0.21725 | 0.247846 | intron-variant | PHF21A | GRCh38.p7 | 11:46014066 | GTTTCTTATAACAGC[A/G]TATTTCATAATGCTG | 51317 |
rs61882535 | snp | A/G | 0.217851 | 0.247924 | intron-variant | PHF21A | GRCh38.p7 | 11:46017010 | GAGTCTCACTCTGTC[A/G]CCCAGGCTGGAGTGC | 51317 |
rs61882536 | snp | A/G | 0.206336 | 0.246157 | intron-variant | PHF21A | GRCh38.p7 | 11:46018399 | TTCAGGAGAATGTAC[A/G]GTATAGTATTAACAC | 51317 |
rs61882537 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46019099 | TTTTTTTTTTTTTTA[A/T]TTTGGAGCCTTTGAA | 51317 |
rs61882538 | snp | C/T | 0.21725 | 0.247846 | intron-variant | PHF21A | GRCh38.p7 | 11:46024778 | GCACTCCAGCCTGGG[C/T]GACCAAGTGAGACTC | 51317 |
rs61882539 | snp | A/G | 0.205723 | 0.246048 | intron-variant | PHF21A | GRCh38.p7 | 11:46031797 | TTACTAACACTATAC[A/G]CAAAAGCTGGAAGAA | 51317 |
rs61882540 | snp | A/T | 0.205723 | 0.246048 | intron-variant | PHF21A | GRCh38.p7 | 11:46032209 | AGCGAAAATATCATT[A/T]TATTTTCCTATTTAT | 51317 |
rs61882541 | snp | A/G | 0.21303 | 0.247251 | intron-variant | PHF21A | GRCh38.p7 | 11:46033012 | TCCTTCTGCCCAAAA[A/G]GTAGTTACTATTCTG | 51317 |
rs61882542 | snp | C/T | 0.21303 | 0.247251 | intron-variant | PHF21A | GRCh38.p7 | 11:46033068 | ATAATTATCCATATA[C/T]AATGTTTTATTAGTT | 51317 |
rs61882543 | snp | C/T | 0.167809 | 0.236103 | intron-variant | PHF21A | GRCh38.p7 | 11:46037632 | TGGACAAGAGTGAAA[C/T]GTCATCTCAAAAAAA | 51317 |
rs61882544 | snp | A/G | 0.168135 | 0.236216 | intron-variant | PHF21A | GRCh38.p7 | 11:46038424 | TGTGCCACTGCACCC[A/G]GCCCATTTCATTCTT | 51317 |
rs61882545 | snp | C/T | 0.167484 | 0.23599 | intron-variant | PHF21A | GRCh38.p7 | 11:46038975 | GCAGAGAAAACAGTG[C/T]TATAAAGACCTAAGG | 51317 |
rs61882546 | snp | C/G | 0.166832 | 0.235761 | intron-variant | PHF21A | GRCh38.p7 | 11:46039014 | AGTTTGACATGAACA[C/G]AGAACAGCAAGGAGC | 51317 |
rs61882547 | snp | C/G | 0.167158 | 0.235875 | intron-variant | PHF21A | GRCh38.p7 | 11:46040449 | TAGAAGAGAAAATGT[C/G]TGAATAGTGATATTT | 51317 |
rs61882548 | snp | G/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46042248 | ATATTCCTCAATAAG[G/T]CATATTCCATATTTT | 51317 |
rs61882549 | snp | C/T | 0.0297652 | 0.118307 | intron-variant | PHF21A | GRCh38.p7 | 11:46049384 | CCATTAGGTTGAACC[C/T]GGCCCAAATACATAC | 51317 |
rs61882550 | snp | C/T | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46060367 | TTCAACTCCTAATGC[C/T]AATATTCTAGTCTCC | 51317 |
rs61882551 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46068667 | ATAGATGAGCAAAGT[A/G]GAAAAAAAAAATACA | 51317 |
rs61884079 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46094752 | ATACAAAAAAAAAAT[A/T]AGCTGGGTATGGTGG | 51317 |
rs61884080 | snp | A/G | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46119741 | TCGCGAACGTGGTCA[A/G]GGGAAAAAAAAAAAA | 51317 |
rs61884081 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:46121191 | CACTCACTCTCTCTC[C/T]CTCTCTCTCTCTGGG | 51317 |
rs61884082 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:46121192 | ACTCACTCTCTCTCT[C/G]TCTCTCTCTCTGGGC | 51317 |
rs66486473 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45962689 | CTGAGGTCAGGAGTC[-/T]GAGACCAGCCTGGCC | 51317 |
rs66525187 | in-del | -/A | 0.272241 | 0.249009 | intron-variant | PHF21A | GRCh38.p7 | 11:45967368 | GTGAGACCCTGTCTT[-/A]AAAAAAAAAAAAAAA | 51317 |
rs66611953 | in-del | -/T | 0.353371 | 0.227628 | intron-variant | PHF21A | GRCh38.p7 | 11:45970582 | GGATTTTTTTTTTTT[-/T]CCTGAACAAAACTTG | 51317 |
rs67051629 | in-del | -/T | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46074462 | ATATGCCTTCCCCCC[-/T]CCCGCCAAAAGAGCC | 51317 |
rs67140459 | in-del | -/GTT | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45961641 | CTGAATTGACGACAT[-/GTT]ACATAGAAGTCTTTG | 51317 |
rs67219578 | in-del | -/A | 0.204189 | 0.245767 | intron-variant | PHF21A | GRCh38.p7 | 11:46095188 | CATTTGGAAATTGTC[-/A]AAAAAAAAAGCAAAT | 51317 |
rs67231476 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46108588 | TATATATATATATAA[-/T]AATACATATGTAAAT | 51317 |
rs67513675 | in-del | -/CT | 0.209997 | 0.246779 | intron-variant | PHF21A | GRCh38.p7 | 11:45962674 | AGGCAGGTGGGTCGC[-/CT]GAGGTCAGGAGTCTG | 51317 |
rs67737247 | in-del | -/TGT | 0.217851 | 0.247924 | intron-variant | PHF21A | GRCh38.p7 | 11:45961640 | TCTGAATTGACGACA[-/TGT]TACATAGAAGTCTTT | 51317 |
rs67867185 | multinucleotide-polymorphism | AC/GA | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45976635 | ATCACTTGAGCTCCG[AC/GA]GTTTGAGACCAGCCT | 51317 |
rs71038877 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45987661 | TTTTTTTTTTTTTTT[-/T]TGAGACGGGGTCTTG | 51317 |
rs71038878 | in-del | -/AC | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46021559 | AGACCCTGTCTCTGA[-/AC]ACACACACACACATG | 51317 |
rs71038879 | in-del | -/ACAC | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46030870 | AAATTGCTACTGGAA[-/ACAC]ACACACACACACACA | 51317 |
rs71038882 | in-del | -/GTGT | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46099560 | GTGTTTGTGTTTAGG[-/GTGT]GTGTGTGTGTGTGTG | 51317 |
rs71308367 | multinucleotide-polymorphism | ATA/GTG | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45958443 | TGTGTGTGTGTGTGT[ATA/GTG]TATATATATATATAT | 51317 |
rs71451628 | in-del | -/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46028092 | AATCTCTGGGGACAA[-/T]TTTTTTTTTTTTGAA | 51317 |
rs71451629 | in-del | -/GG | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46040476 | TTTAAAAAGTGGGGA[-/GG]GGGGTGACGGCTTGG | 51317 |
rs71491886 | snp | G/T | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45972145 | TGAAACATGACAAGG[G/T]GAAAACAAACATCTG | 51317 |
rs71491887 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | PHF21A | GRCh38.p7 | 11:46024150 | TATATGTTGGGCTAA[C/T]TGAGTTGCTGGTCCT | 51317 |
rs71491888 | snp | C/T | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46112522 | AAAAAATTTAAACTT[C/T]CCAAATAAAAATATA | 51317 |
rs71491889 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | PHF21A | GRCh38.p7 | 11:46113354 | TCTCTAGCACATACC[A/G]GAAAAAGTATCAATA | 51317 |
rs72047907 | in-del | -/ATAA | 0.463881 | 0.12944 | intron-variant | PHF21A | GRCh38.p7 | 11:46108585 | TATATATATATATAT[-/ATAA]AATACATATGTAAAT | 51317 |
rs72169233 | in-del | -/AC | | | intron-variant | PHF21A | GRCh38.p7 | 11:46099524 | CTATAGAAAAATTAG[-/AC]ACACACACACACACA | 51317 |
rs72350091 | in-del | -/TATG | | | intron-variant | PHF21A | GRCh38.p7 | 11:45987259 | TAAATAAATGTATGT[-/TATG]ATGTATGTATGTATG | 51317 |
rs72392141 | in-del | -/CACACC/CACC/CAGACACC/CC | | | intron-variant | PHF21A | GRCh38.p7 | 11:46099556 | ACACACACACACACA[-/CACACC/CACC/CAGACACC/CC]CACACACCCTAAACA | 51317 |
rs72904359 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | PHF21A | GRCh38.p7 | 11:46004407 | GGAAATGGATTTCAC[C/T]TTTAATAGATAAGAA | 51317 |
rs72904367 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46014598 | TCCAAATGGCCGAGG[C/T]TGAACTAATTTACAT | 51317 |
rs72904369 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46015419 | AAATTCTTTGCCTAG[A/G]CCAATTTCCAGAAAA | 51317 |
rs72904370 | snp | C/G | 0.264358 | 0.249587 | intron-variant | PHF21A | GRCh38.p7 | 11:46018464 | TCTATAGGGGAAAAA[C/G]AAAAGAATCTCCTTA | 51317 |
rs72904373 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46034978 | CAGAGTTAGCCTACC[A/G]TAGTTAAAAATGAAG | 51317 |
rs72904383 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46053266 | GATTTACAAAATATC[A/G]ATATGAAAGAATTAT | 51317 |
rs72904393 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | PHF21A | GRCh38.p7 | 11:46080566 | CCTTACAAAAAAGGT[C/T]CCAAACTACTATGTG | 51317 |
rs72904397 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PHF21A | GRCh38.p7 | 11:46083755 | ACATTTTCTTTAAGA[C/T]TGGAATCAACGCATA | 51317 |
rs72906234 | snp | A/G | 0.0785177 | 0.181917 | intron-variant | PHF21A | GRCh38.p7 | 11:46109335 | GTAAAAAGGCTTAGC[A/G]CTATACATAATAAAC | 51317 |
rs73450035 | snp | G/T | 0.0372196 | 0.131242 | intron-variant | PHF21A | GRCh38.p7 | 11:45958647 | ATAGACCAGGCTTGG[G/T]GTTCATGCCTATAAT | 51317 |
rs73450051 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | PHF21A | GRCh38.p7 | 11:45978946 | TCCCATCAGTGTATT[A/G]GAACAAATACATTTT | 51317 |
rs73452216 | snp | C/T | 0.205723 | 0.246048 | intron-variant | PHF21A | GRCh38.p7 | 11:46021167 | TGAGCTCAAGTGATC[C/T]TCCCACCTCAGCTTC | 51317 |
rs73453956 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | PHF21A | GRCh38.p7 | 11:46037125 | TTGATCTCAAAGACT[C/T]ATTTTTTGGTTTTGT | 51317 |
rs73453970 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | PHF21A | GRCh38.p7 | 11:46052868 | GATGAATAAGCAAAG[A/G]CATCACAGAAAGGGA | 51317 |
rs73455946 | snp | A/T | 0.0667028 | 0.170006 | intron-variant | PHF21A | GRCh38.p7 | 11:46094914 | AAAAAAAGACAAATC[A/T]TGAAATCCTTTAAAC | 51317 |
rs73455987 | snp | C/T | 0.10237 | 0.201756 | intron-variant | PHF21A | GRCh38.p7 | 11:46108197 | TTTTTTTAAATGTTA[C/T]TTGAAAACACAATTG | 51317 |
rs73457804 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | PHF21A | GRCh38.p7 | 11:46115720 | AGTTCTAGATATAGA[C/T]ATAAAAGAATTCCAT | 51317 |
rs73457874 | snp | G/T | 0.5 | 0 | upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46122305 | AGGCAACAGGAGAAA[G/T]ATGCAACCTCAAGTC | 51317 |
rs74347080 | snp | C/G | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45968931 | AGCGAAACTCCATTG[C/G]AAAAAAAAAAAAAAA | 51317 |
rs74366855 | snp | A/T | 0.498525 | 0.0271165 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46120272 | TTAAATAAATAATCA[A/T]AATAAAAACTTCCCC | 51317 |
rs74402481 | snp | A/T | 0.0592355 | 0.161582 | intron-variant | PHF21A | GRCh38.p7 | 11:46072354 | CTAGTAAACATCCTT[A/T]AAAAATAAAGGGCTT | 51317 |
rs74412263 | snp | A/G | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46117341 | AACAGAGTTTCAAAG[A/G]ACCATGTGCTATAAA | 51317 |
rs74534275 | snp | A/G | 0.0146672 | 0.084371 | upstream-variant-2KB | PHF21A, LOC105376661 | GRCh38.p7 | 11:46123177 | CCAAAGTCAAAGTGA[A/G]TCATTCGCAGAACCA | 51317 |
rs74566099 | snp | A/G | 0.0119091 | 0.0762411 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45931553 | GGGAAGATGAAAGGC[A/G]ATGGCTGATAGAGAT | 51317 |
rs74574566 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | PHF21A | GRCh38.p7 | 11:46111797 | AAAGAGAAAATTAAT[A/G]TAAAGAATTAAGATT | 51317 |
rs74628904 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | PHF21A | GRCh38.p7 | 11:45989238 | TTCAGAATTTCAGAA[C/T]ACATTTGCTTTTGTT | 51317 |
rs74656235 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46010655 | AAACAATCTTGGCTG[C/T]GGAAGAAATAACAGG | 51317 |
rs74675384 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | PHF21A | GRCh38.p7 | 11:46075444 | ATAAGGAGGCTCAGC[A/G]CTAACAGAATTCTAA | 51317 |
rs74731612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46068540 | CATTCTGAAATACAG[A/G]TATGTTCTATGCAAA | 51317 |
rs74742526 | snp | C/G | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45976623 | GAGATGGGTGGATCA[C/G]TTGAGCTCCGGAGTT | 51317 |
rs74893293 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:45973592 | GGATCACCTATCTTC[A/G]ATCAGTGATGAAAAC | 51317 |
rs74945666 | in-del | -/G | 0.347032 | 0.230401 | intron-variant | PHF21A | GRCh38.p7 | 11:46032479 | ACAAATACACCAAAT[-/G]TTTTTTTCAATTCTC | 51317 |
rs75013512 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45940163 | CTACACAAGTTTTAA[A/G]ATACATCATAGTGTG | 51317 |
rs75019001 | snp | A/C | 0.0592355 | 0.161582 | intron-variant | PHF21A | GRCh38.p7 | 11:45934402 | TACCACCTAAGGAAC[A/C]GGGCGGGTGGAGTGG | 51317 |
rs75045371 | snp | A/C | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46073328 | GCGAGACCCCGTCTC[A/C]AAAAAAAAAAAAAAA | 51317 |
rs75056090 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | PHF21A | GRCh38.p7 | 11:46018846 | TGCTTACTGCATACC[A/G]TGACACGCTCTCACA | 51317 |
rs75062866 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | PHF21A | GRCh38.p7 | 11:46031728 | TTCCTCTGGCTTTGT[C/T]TGTTAGGTCTAATAG | 51317 |
rs75069630 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | PHF21A | GRCh38.p7 | 11:45951157 | CTTCATTTTCTGTTG[G/T]ACTACTGCATGCAGT | 51317 |
rs75080425 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | PHF21A | GRCh38.p7 | 11:45996530 | GAGAGAGAGAGAAAC[A/G]TATTCCATTAATAAT | 51317 |
rs75156306 | snp | A/T | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46108588 | ATATATATATATATA[A/T]AATACATATGTAAAT | 51317 |
rs75162194 | snp | A/C | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46088544 | ACCATCCCAAAAAAC[A/C]AAAAATGCTAATTCT | 51317 |
rs75193857 | snp | A/T | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45971905 | CTTTTTTTTTTTTTT[A/T]ATGGTGTCACCCTGG | 51317 |
rs75215311 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | PHF21A | GRCh38.p7 | 11:46071358 | GCAAGTTCAGCCAGC[A/C]CACAAACTGAAGCAG | 51317 |
rs75220124 | snp | A/G | | | upstream-variant-2KB | PHF21A, LOC105376661 | GRCh38.p7 | 11:46122746 | TTGGCGGGGSGGGGG[A/G]GGGCCTTTTTTTTTT | 51317 |
rs75278456 | snp | A/C/G | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46117339 | CTAACAGAGTTTCAA[A/C/G]GGACCATGTGCTATA | 51317 |
rs75294714 | snp | C/T | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46043644 | CATTAAAAAAAAAAA[C/T]TGACCCACTTTTAGA | 51317 |
rs75337344 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46010658 | CAATCTTGGCTGTGG[A/T]AGAAATAACAGGTTT | 51317 |
rs75340687 | snp | A/T | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45998530 | TTTCTTTTTTTTTTT[A/T]AAACAGAGTTTTGCT | 51317 |
rs75342021 | snp | A/C | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46018251 | CGAGACTCCGTCTCA[A/C]AAAAAAAAAAAAAAA | 51317 |
rs75354770 | snp | A/T | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46094750 | AAATACAAAAAAAAA[A/T]TTAGCTGGGTATGGT | 51317 |
rs75441023 | snp | A/T | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46025189 | ATATGTATACAGATT[A/T]AAAAAAAAAAACAAC | 51317 |
rs75442850 | snp | A/C | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46048770 | GCAAGACTCCATCTC[A/C]AAAAAAAAATAATTT | 51317 |
rs75471410 | snp | C/T | 0.0696718 | 0.173152 | intron-variant | PHF21A | GRCh38.p7 | 11:46056656 | ACTGTTTCACCTGTA[C/T]GTTTACTTCACCAAT | 51317 |
rs75484531 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45940659 | TCTTCCTTCATTATT[A/T]AAATCAGGCTGAGGG | 51317 |
rs75533862 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | PHF21A | GRCh38.p7 | 11:46071891 | TTAGTTTAAAAAGCA[G/T]AAAAAGCAAGACACA | 51317 |
rs75573459 | snp | A/T | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45992389 | TACAAAAAAAAAAAA[A/T]ATTAGCCAGGCATGG | 51317 |
rs75669091 | snp | G/T | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46110804 | TTTTTTTTTTTTTTT[G/T]AGACAGAGTCTTGCT | 51317 |
rs75680100 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46089049 | TCCATGACACAGTGT[C/G]CCCCAAACTGTCCCT | 51317 |
rs75681436 | snp | A/G | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45990727 | GTTTTTTTTTTTTAA[A/G]GAAGACTTTATTTTT | 51317 |
rs75685721 | snp | C/T | 0.0670745 | 0.170406 | intron-variant | PHF21A | GRCh38.p7 | 11:46098865 | AAGGAGGAGGATCAA[C/T]GCCCAGCACTGCATC | 51317 |
rs75688046 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46016678 | TTTGTAGCTTATGTT[A/C/T]TTCTCCTCTACTATA | 51317 |
rs75713103 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45938832 | AAGGGGGAGACTAGT[A/G]TATTCTTTTTTTTTT | 51317 |
rs75718116 | snp | A/C | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46011491 | TGCAAGATTCAGTCT[A/C]AAAAAAAAAAAAGTG | 51317 |
rs75748207 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46066920 | TTTTAGTATTTTGCA[C/T]TTTAAACTAATACTG | 51317 |
rs75762440 | snp | C/G/T | 0.000486027 | 0.0155813 | splice-acceptor-variant | PHF21A | GRCh38.p7 | 11:45935740 | TCTCTTCTTCTTTTG[C/G/T]TAAAAAAAAAAAAAA | 51317 |
rs75783582 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PHF21A | GRCh38.p7 | 11:46062139 | ATCTTTTATTCTTGT[C/T]TTGCTAAAGTTTCAC | 51317 |
rs75788838 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | PHF21A | GRCh38.p7 | 11:46025829 | AGTCATCGGCAGATA[C/T]GTGATGGAGCAAGTA | 51317 |
rs75796602 | in-del | -/CCCT | | | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46120703 | CTGACGAGAACACCC[-/CCCT]TTCCCTCCTCCCTCC | 51317 |
rs75875668 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | PHF21A | GRCh38.p7 | 11:45985085 | TCAAAATGAAACCAA[A/G]GATACTAAATTTTAC | 51317 |
rs75893373 | snp | A/G | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46014438 | CTAGGTGGGTTCCGT[A/G]TCATTGCTACTGTGA | 51317 |
rs75931605 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PHF21A | GRCh38.p7 | 11:45950768 | TCTTAAAAAGAAGAG[A/G]ATTTCATACTCACAA | 51317 |
rs75940593 | snp | A/G | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45943910 | TGAATCTACTGCTGA[A/G]AAAAAAAATCAGACA | 51317 |
rs75941946 | in-del | -/ATGAACCCACAT | | | intron-variant | PHF21A | GRCh38.p7 | 11:46063831 | ATACTGTTTCATCTG[-/ATGAACCCACAT]CATAGGATAAGCAGA | 51317 |
rs75969129 | snp | A/G | 0.5 | 0 | synonymous-codon, intron-variant, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45971191 | ACTAGACGTCTGGAG[A/G]TTGACTGGTGTGTTC | 51317 |
rs75985978 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:45962078 | GGCCATGCTTCCTTC[C/T]CTGGAGACACAGCCT | 51317 |
rs75993693 | snp | A/C | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45968936 | AACTCCATTGCAAAA[A/C]AAAAAAAAAAAAAAA | 51317 |
rs76142987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46103183 | TTCTTTAACTCAACC[C/T]CCAAACGCTTGTAGA | 51317 |
rs76157357 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45950773 | AAAAGAAGAGGATTT[A/C]ATACTCACAAAACAT | 51317 |
rs76159872 | in-del | -/GCTTTAA | | | intron-variant | PHF21A | GRCh38.p7 | 11:46000507 | TTTAAACAGCTTTAA[-/GCTTTAA]AGACTCTATAACGTT | 51317 |
rs76179056 | snp | A/T | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46112114 | GACAGGCAGAGCTGA[A/T]TACTAGTCAAAATAT | 51317 |
rs76189233 | snp | A/T | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46107860 | CTTACTTTTTTTTTT[A/T]AACTGCGTTAAAAAA | 51317 |
rs76202957 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | PHF21A | GRCh38.p7 | 11:45990179 | ACTAACACAAACATA[C/T]ACACACCCCTCTCAC | 51317 |
rs76227468 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | PHF21A | GRCh38.p7 | 11:45999493 | TAGAAGACTGTTCCT[C/T]GAGACTAGAAAGTAG | 51317 |
rs76252309 | snp | C/T | 0.167809 | 0.236103 | intron-variant | PHF21A | GRCh38.p7 | 11:46042518 | AACCGAAGAAAGAGA[C/T]TGGTGAAATGTATAG | 51317 |
rs76273909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45973776 | ACTTCTGAAGTGGTG[A/G]TCCAGTCACACCAGA | 51317 |
rs76343926 | snp | G/T | | | missense, utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934084 | CCGGGCCATTGGAGA[G/T]GGCCCCCACAGTGGC | 51317 |
rs76350207 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45967781 | TGAACTTAAAACGAC[C/T]CTGTGGTGGGTGCTA | 51317 |
rs76350368 | snp | C/T | 0.0626037 | 0.165477 | intron-variant | PHF21A | GRCh38.p7 | 11:46116584 | TTTTTTTTTAAATTA[C/T]GAGAAACTGACTAGG | 51317 |
rs76362279 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46106786 | GCACTGCCATCTCAA[C/T]GGGAGTAGAAGCTAT | 51317 |
rs76401460 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46036464 | AAAATATTCACTGGA[A/C]TTTTGAAGAGAATTA | 51317 |
rs76438715 | snp | A/T | 0.5 | 0 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:46121181 | CTCTCTCTCTCACTC[A/T]CTCTCTCTCTCTCTC | 51317 |
rs76464147 | snp | C/G | 0.0908922 | 0.192833 | intron-variant | PHF21A | GRCh38.p7 | 11:46046367 | AAAGTATTTCCCCAT[C/G]AAGCAAAATGAGAGA | 51317 |
rs76477043 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | PHF21A | GRCh38.p7 | 11:46056507 | CAAGAAATTGGGCTT[C/T]TAAAAAATAGGTCCT | 51317 |
rs76477049 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45940660 | CTTCCTTCATTATTA[A/T]AATCAGGCTGAGGGC | 51317 |
rs76487165 | snp | A/C | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46073327 | AGCGAGACCCCGTCT[A/C]AAAAAAAAAAAAAAA | 51317 |
rs76497265 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | PHF21A | GRCh38.p7 | 11:46016833 | TAGAATGCAGACCTA[C/T]AGCACTTAAAAATTA | 51317 |
rs76518673 | snp | G/T | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45979034 | TTCTTTTTTTTTTTT[G/T]GAGACGGAGTTTTGC | 51317 |
rs76578966 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:45992805 | AAAATGGTAGTAATA[C/T]GTTTCATAATGGTGC | 51317 |
rs76595296 | in-del | -/A | 0.406641 | 0.194842 | intron-variant | PHF21A | GRCh38.p7 | 11:46083169 | AACAGAAGCAAAGTT[-/A]AAAAAAAAAAAAAGT | 51317 |
rs76612666 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | PHF21A | GRCh38.p7 | 11:46003583 | TTCACGAAGGGCAGA[A/G]TGAGAAAACGCTACA | 51317 |
rs76687821 | snp | G/T | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46110802 | AATTTTTTTTTTTTT[G/T]TGAGACAGAGTCTTG | 51317 |
rs76754758 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | PHF21A | GRCh38.p7 | 11:46067379 | TTCTGAGGTAAGTGA[A/C]GTAGTAACATTGCAG | 51317 |
rs76768713 | snp | A/G | 0.0689305 | 0.172377 | intron-variant | PHF21A | GRCh38.p7 | 11:45982337 | GCCAATTTTGGGGGG[A/G]AAAATTCTGCTATGC | 51317 |
rs76773787 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:45991019 | ACTGTCCTGAAATTC[C/T]TCTATGCCTGTCTAT | 51317 |
rs76787394 | snp | A/C | | | missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45965444 | GGTTGCAGTCTGCCC[A/C]TTGACGACACGGACG | 51317 |
rs76858304 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | PHF21A | GRCh38.p7 | 11:46107342 | AGTTTCACCATCCAT[A/G]ACATTAATTGAGCCC | 51317 |
rs76860471 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46052654 | TGAAGCTAAATTGCT[A/C]CTAGCTGCTAGTGCT | 51317 |
rs76981344 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45940166 | CACAAGTTTTAAGAT[A/C]CATCATAGTGTGGAT | 51317 |
rs76999280 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PHF21A | GRCh38.p7 | 11:45959290 | ATCATTTCACTATGT[A/G]TATGTATATCAAACC | 51317 |
rs77023116 | snp | C/T | 0.00230031 | 0.0338358 | intron-variant | PHF21A | GRCh38.p7 | 11:45953645 | GAGAGAAAAATTAAA[C/T]AAAAATTCAGAATTC | 51317 |
rs77041824 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | PHF21A | GRCh38.p7 | 11:45941513 | GCAAATGATGGTTTA[C/G]TATCATTATGAAAAT | 51317 |
rs77135563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46065013 | TATTTCAGCATGCAT[A/G]TACCTTTAGATATAC | 51317 |
rs77155449 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46093680 | AAAGGTTGCCTCAAA[C/G]AGTACCAGGCACATA | 51317 |
rs77171173 | in-del | -/ATT | | | intron-variant | PHF21A | GRCh38.p7 | 11:45974454 | ATTATTATTATTATT[-/ATT]GCTGTTTATTTATTT | 51317 |
rs77199455 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:45950774 | AAAGAAGAGGATTTC[A/C]TACTCACAAAACATG | 51317 |
rs77205953 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46119413 | TCATTTTAAAAACAA[C/T]ACAATGTGGACGTGC | 51317 |
rs77207490 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PHF21A | GRCh38.p7 | 11:46031761 | TCTGGAAAAGAATGC[A/G]ATAATTTTTTTCCAG | 51317 |
rs77231570 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46068373 | TGGATTTTTTGAAAG[C/G]ATACATATATATAAT | 51317 |
rs77314809 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | PHF21A | GRCh38.p7 | 11:45992759 | ACACAGGGAAACACA[C/T]AACTATATACAAAAT | 51317 |
rs77425178 | snp | G/T | 0.0524604 | 0.153226 | intron-variant | PHF21A | GRCh38.p7 | 11:46064508 | AAACTTGGGAGTAAA[G/T]CAACTTTGGGAAACA | 51317 |
rs77474453 | snp | A/T | 0.0509478 | 0.151255 | intron-variant | PHF21A | GRCh38.p7 | 11:46068111 | AGAATTTATGGGGTA[A/T]GTATGAGAATGAGTT | 51317 |
rs77509405 | snp | A/C | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46107862 | TACTTTTTTTTTTTA[A/C]CTGCGTTAAAAAATA | 51317 |
rs77537001 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | PHF21A | GRCh38.p7 | 11:45946217 | GACTCTCAAGAGAAG[A/G]GAGGATAAGAGAGCT | 51317 |
rs77552714 | snp | C/T | 0.0883596 | 0.190715 | intron-variant | PHF21A | GRCh38.p7 | 11:45994410 | CTGCGGAAATACCAT[C/T]ACAAACCACACAGAG | 51317 |
rs77580310 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45962311 | ACGGGTTTGGTAACT[C/G]TGAACAGGTGTGAAC | 51317 |
rs77589058 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46036236 | TGGTAGACTGTGGTA[A/G]AATTTACAGTCATAA | 51317 |
rs77642428 | snp | C/G | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45986348 | TAATATTGATATAGT[C/G]AGACTTTGCCTAAAT | 51317 |
rs77687899 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | PHF21A, LOC105376661 | GRCh38.p7 | 11:46123210 | AATAGCCTTGGACTT[C/T]ACTAGTCACATCTTT | 51317 |
rs77717223 | snp | A/T | 0.5 | 0 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:46121173 | CTCCTCTCCTCTCTC[A/T]CTCACTCACTCTCTC | 51317 |
rs77828251 | snp | G/T | 0.0581099 | 0.160244 | intron-variant | PHF21A | GRCh38.p7 | 11:46083592 | GTATGTGTGTCTTCC[G/T]CCTGATGTCCAGCTA | 51317 |
rs77845739 | snp | G/T | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46015095 | GCATTTCTTTGATGA[G/T]TAGCAATGTTGAGCA | 51317 |
rs77858224 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PHF21A | GRCh38.p7 | 11:46061882 | AGATGTATGGGAGGT[A/G]AGTTTTGTGACCTTG | 51317 |
rs77892629 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | PHF21A | GRCh38.p7 | 11:46047372 | GTTTATCATGAAGCA[C/T]TTTTATAGGCTGGTA | 51317 |
rs77896334 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45954443 | ACCACCCTTACATGG[A/T]ATATTAAAAATCTGT | 51317 |
rs77931661 | snp | A/C | 0.167809 | 0.236103 | intron-variant | PHF21A | GRCh38.p7 | 11:46035451 | ATTCACTTAATGTAC[A/C]TATTCAGTACACTAC | 51317 |
rs77991256 | snp | C/T | 0.0655868 | 0.168795 | intron-variant | PHF21A | GRCh38.p7 | 11:46114394 | GTTATTTTCAGGCAA[C/T]AGCACCTTCACAAAC | 51317 |
rs78017238 | snp | C/T | 0.0670745 | 0.170406 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45929731 | AGAGCCCTGCTTCCG[C/T]TTAGAGGAGGTATTT | 51317 |
rs78048536 | snp | A/C | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46043643 | CCATTAAAAAAAAAA[A/C]CTGACCCACTTTTAG | 51317 |
rs78076010 | snp | C/T | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45998534 | TTTTTTTTTTTTAAA[C/T]AGAGTTTTGCTCTTG | 51317 |
rs78076847 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | PHF21A | GRCh38.p7 | 11:46076470 | ACTGCCTTTACCCCA[A/T]CCCCTATAGGTAAAC | 51317 |
rs78077668 | snp | A/T | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46018712 | GATATGGACAACACA[A/T]TTTTTTTTTTAAATT | 51317 |
rs78131170 | snp | A/G | 0.0887219 | 0.191022 | intron-variant | PHF21A | GRCh38.p7 | 11:46047096 | AAATGTAGTTGACCA[A/G]ATAAATATCACTAGG | 51317 |
rs78192606 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | PHF21A | GRCh38.p7 | 11:45983092 | AGGAGCAAGGGATGC[A/G]GGCTAGAGTACTACT | 51317 |
rs78216584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46038434 | CACCCGGCCCATTTC[A/G]TTCTTTCAATAACTA | 51317 |
rs78252352 | snp | C/G | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45992873 | ATTTAACCCCTGTCA[C/G]ATAAGACTGACACAA | 51317 |
rs78263266 | snp | C/T | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46007321 | TTTTCTTCTTCTTCT[C/T]TTTTTTTTTTTCGAG | 51317 |
rs78293345 | in-del | -/T | 0.49953 | 0.0153219 | intron-variant | PHF21A | GRCh38.p7 | 11:46016972 | AATGTTTAACCTGGA[-/T]TTTTTTTTTTTTAAT | 51317 |
rs78316938 | snp | C/T | 0.0876345 | 0.190099 | intron-variant | PHF21A | GRCh38.p7 | 11:45969610 | CCCTTTCCTTTACTT[C/T]CCCCTGCTACTGCCT | 51317 |
rs78324587 | snp | G/T | 0.0341408 | 0.126114 | intron-variant | PHF21A | GRCh38.p7 | 11:46020981 | ACGATAGTTTCAATG[G/T]ATGATGGGTTTATTG | 51317 |
rs78329000 | snp | G/T | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46032479 | ACAAATACACCAAAT[G/T]TTTTTTTCAATTCTC | 51317 |
rs78335501 | snp | G/T | 0.0376037 | 0.131863 | intron-variant | PHF21A | GRCh38.p7 | 11:46096158 | CTTAATAACCATCCC[G/T]CTTGTACCCACCTCT | 51317 |
rs78336078 | snp | C/T | 0.277778 | 0.248452 | intron-variant | PHF21A | GRCh38.p7 | 11:46044671 | TAAACATTCTCATTT[C/T]TAAGCAAACAGGCCA | 51317 |
rs78353736 | snp | A/G | 0.111928 | 0.208413 | intron-variant | PHF21A | GRCh38.p7 | 11:46006959 | AGATAACAATAACAA[A/G]AGCTATTATTTACTT | 51317 |
rs78356303 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | PHF21A | GRCh38.p7 | 11:46024498 | TCCTCTATACTTTAA[A/T]TAAGACTTAGGGACT | 51317 |
rs78361352 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | PHF21A | GRCh38.p7 | 11:45973200 | CAAATGTCAAAAGTC[A/G]CATGTGGTTAGTGGT | 51317 |
rs78392288 | snp | C/T | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45990252 | GCATTTTCATCTTCT[C/T]TTTTTTTTTTTTTTT | 51317 |
rs78393756 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | PHF21A | GRCh38.p7 | 11:45988537 | CTCTTGATGCTTAAA[A/T]TCATAATTTAAAAAA | 51317 |
rs78452453 | in-del | -/GG | | | upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46122223 | TTTGAAGGGGGGGGG[-/GG]AAAGCCGTGAGGGGC | 51317 |
rs78566865 | snp | A/T | 0.0166325 | 0.0896639 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45931017 | TTTGAGTGCAGAATG[A/T]AGGTTTGGGGGCTGG | 51317 |
rs78579936 | snp | C/T | 0.0520825 | 0.152737 | intron-variant | PHF21A | GRCh38.p7 | 11:46049837 | TAGCACTGAGAACCA[C/T]AGGTTCCTAAAAACA | 51317 |
rs78607403 | snp | C/T | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46029972 | GATAGTCTTTATAAC[C/T]TGATTTGATAAATAT | 51317 |
rs78614507 | snp | A/C | 0.0872718 | 0.189788 | intron-variant | PHF21A | GRCh38.p7 | 11:46018698 | ATGAACAAAATCCTG[A/C]TATGGACAACACATT | 51317 |
rs78673241 | snp | A/T | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46043645 | ATTAAAAAAAAAAAC[A/T]GACCCACTTTTAGAA | 51317 |
rs78677379 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46010656 | AACAATCTTGGCTGT[C/G]GAAGAAATAACAGGT | 51317 |
rs78690620 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | PHF21A | GRCh38.p7 | 11:46040741 | ATTCTGTATATGTTC[A/G]AATTTAAATACCACT | 51317 |
rs78717996 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46084695 | ATTTTTTTTTTTTTT[G/T]TTGAGATGGAGTCTC | 51317 |
rs78757473 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PHF21A | GRCh38.p7 | 11:46100880 | AGTTTCTAACCACTG[C/T]TACCACGTCTAAAGA | 51317 |
rs78818556 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46010657 | ACAATCTTGGCTGTG[A/G/T]AAGAAATAACAGGTT | 51317 |
rs78883214 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46092163 | CAGGCACACGATGTC[C/T]ACCTAGTCAAAGTAC | 51317 |
rs78902975 | snp | A/T | 0.0193772 | 0.0965046 | intron-variant | PHF21A | GRCh38.p7 | 11:46069708 | GATTCTAGTATTGAA[A/T]CTCATACTGATAAAT | 51317 |
rs78909054 | snp | A/T | 0 | 0 | splice-acceptor-variant | PHF21A | GRCh38.p7 | 11:45935741 | CTCTTCTTCTTTTGC[A/T]AAAAAAAAAAAAAAA | 51317 |
rs78915745 | snp | G/T | 0.0267878 | 0.112589 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45929929 | GGGTGCCCGGCAGAG[G/T]GACAGGGGCGAGGTT | 51317 |
rs78917538 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | PHF21A | GRCh38.p7 | 11:46110736 | AGACCAGATTCCATA[A/C]ATTTTGGACACATCT | 51317 |
rs78927968 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | PHF21A | GRCh38.p7 | 11:46106512 | TTGGGGGAAGTAAAC[A/G]AATACTAAATAGAAT | 51317 |
rs78929317 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | PHF21A | GRCh38.p7 | 11:46025364 | ATTTTAGTTGGTTTT[C/T]AGGTCAAATTCAAAT | 51317 |
rs78952518 | snp | A/C | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46011492 | GCAAGATTCAGTCTC[A/C]AAAAAAAAAAAGTGT | 51317 |
rs78988100 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | PHF21A | GRCh38.p7 | 11:45985065 | TCTTCAGACACACCA[A/G]TTGCTCAAAATGAAA | 51317 |
rs78990218 | snp | C/T | 0.030278 | 0.119257 | intron-variant | PHF21A | GRCh38.p7 | 11:46029149 | AACTCAAGAAGTCAA[C/T]GATAACTTCTTGTCT | 51317 |
rs79003123 | snp | A/G | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45963437 | AAAAAAAAAAAAAAA[A/G]AGAAAAGAAAAAAAA | 51317 |
rs79050728 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | PHF21A | GRCh38.p7 | 11:45989352 | AATAAAACAAATTTG[A/G]TTAAAAATTTAGCTG | 51317 |
rs79053074 | snp | A/C | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46072902 | CTACAAGAAAGCAAA[A/C]TGAAAGCAGAGAACT | 51317 |
rs79116018 | snp | A/T | 0.0379877 | 0.132479 | intron-variant | PHF21A | GRCh38.p7 | 11:46055280 | GCATTAAATTATGGA[A/T]TTCATGAAAACAACT | 51317 |
rs79124248 | snp | C/T | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46101859 | CGTGCTGGTCTCCCT[C/T]TTTTTTTTTTTTTTT | 51317 |
rs79135806 | snp | C/T | 0.103438 | 0.202533 | intron-variant | PHF21A | GRCh38.p7 | 11:45968015 | ACTGTTTGAAAAACA[C/T]GGACTAAACCTTAGA | 51317 |
rs79161565 | snp | A/T | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45992392 | AAAAAAAAAAAAAAT[A/T]AGCCAGGCATGGTGG | 51317 |
rs79170282 | snp | A/C | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45990247 | TTATAGCATTTTCAT[A/C]TTCTTTTTTTTTTTT | 51317 |
rs79181301 | snp | A/T | 0.0107246 | 0.0724382 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45931383 | GCCAACGATTCCTCC[A/T]ACTAGTCCAGGCATC | 51317 |
rs79225771 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | PHF21A | GRCh38.p7 | 11:46006393 | TAATAAGCACCTAAC[A/G]AAATATTGCAACTTG | 51317 |
rs79294034 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | PHF21A | GRCh38.p7 | 11:46087630 | AACAAATTACAGACA[A/T]GTATTTATAGTTTAC | 51317 |
rs79333080 | snp | A/G | 0.0626037 | 0.165477 | intron-variant | PHF21A | GRCh38.p7 | 11:46087450 | GGACTCTAAATGCCA[A/G]TTACTCATTTTATTT | 51317 |
rs79363736 | snp | C/T | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46101862 | GCTGGTCTCCCTCTT[C/T]TTTTTTTTTTTTTTA | 51317 |
rs79368845 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | PHF21A | GRCh38.p7 | 11:46083946 | TATGAAAAAAATCTT[C/T]TCAGTTCTTTTCTCT | 51317 |
rs79404237 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | PHF21A | GRCh38.p7 | 11:45978979 | TATAAATATGGGCTT[A/T]AAAATGAGTGTTTCT | 51317 |
rs79409023 | snp | A/G | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45943911 | GAATCTACTGCTGAG[A/G]AAAAAAATCAGACAA | 51317 |
rs79438581 | snp | G/T | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46053585 | GAACCCCATGGCTCA[G/T]CATGGGGTTCTAACC | 51317 |
rs79471312 | snp | C/T | 0.0883596 | 0.190715 | intron-variant | PHF21A | GRCh38.p7 | 11:46015138 | TGTTGACTGCTTGTA[C/T]GTCTCCCTTCAAAAG | 51317 |
rs79492020 | snp | A/T | 0.279991 | 0.248195 | intron-variant | PHF21A | GRCh38.p7 | 11:45974930 | TACATGGCATGGCAA[A/T]TACTGCCAATAGCAA | 51317 |
rs79550883 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PHF21A | GRCh38.p7 | 11:45944527 | GCCACAAAGCCCTGC[A/G]CAACTGGCCCAGCCA | 51317 |
rs79610670 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:45987919 | ACTACAGAAATTCTC[C/T]CATTCCTCTGCACTG | 51317 |
rs79635709 | snp | A/C | 0.0217236 | 0.101931 | intron-variant | PHF21A | GRCh38.p7 | 11:46033881 | CTCTAGAGTATATAT[A/C]TAGGAGGAGAACTGG | 51317 |
rs79674682 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | PHF21A | GRCh38.p7 | 11:46050134 | CTTCACGCCAAGTTT[C/T]AGAAAGAAGAGATAC | 51317 |
rs79686965 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | PHF21A | GRCh38.p7 | 11:45999358 | TATTACTTTGCAGAA[A/G]TGGAGTAAGGCAAGT | 51317 |
rs79728014 | snp | A/G | 0.111928 | 0.208413 | intron-variant | PHF21A | GRCh38.p7 | 11:46040694 | CCTGAAGCAGCTTAC[A/G]TGAAACTGCATACTA | 51317 |
rs79767061 | snp | A/G | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46010084 | TCATACTAAAAGAAA[A/G]GGGAGAAAAATATGC | 51317 |
rs79789896 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | PHF21A | GRCh38.p7 | 11:45999153 | ATTTCTTACAGAGTA[G/T]CAACAAAGAAAATTA | 51317 |
rs79805679 | snp | C/G | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45996959 | TATGGTACAGTGAAT[C/G]TGATAATCACAAAAT | 51317 |
rs79836536 | snp | C/T | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46019992 | TTCTACATTTTGACT[C/T]TTTTTTTTTTTAGCC | 51317 |
rs79841873 | in-del | -/GAA | 0.205723 | 0.246048 | intron-variant | PHF21A | GRCh38.p7 | 11:46002669 | TTTAAGGGATATAAT[-/GAA]GAACTTTGGACTCTG | 51317 |
rs79858640 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PHF21A | GRCh38.p7 | 11:45993758 | GTAGAGTAACCTACA[C/T]AATAAATTGAAAGGG | 51317 |
rs79871563 | snp | A/G | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45968930 | GAGCGAAACTCCATT[A/G]CAAAAAAAAAAAAAA | 51317 |
rs79902180 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46090631 | TTACTTGACCACAGA[A/C]GCCTTTTCCCACCCC | 51317 |
rs79911762 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | PHF21A | GRCh38.p7 | 11:46114590 | GTCCATAAGGCCAGA[G/T]ATAGCAGTTGCCATG | 51317 |
rs79942790 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:45977095 | CAACACAGACTACCA[A/G]GGAAAGGAAAAGCTA | 51317 |
rs79981700 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | PHF21A | GRCh38.p7 | 11:45939750 | CAGATCTACTTAAAA[C/T]TGGAAGAGGAGAACA | 51317 |
rs79992266 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46018304 | CTTTCTTATAAAAGC[A/T]TCAAAATGTACCTCC | 51317 |
rs79995370 | snp | A/T | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45974630 | GGCTAATTTTTTTTA[A/T]TTTTAGTAGAGACGT | 51317 |
rs80032902 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | PHF21A | GRCh38.p7 | 11:46079485 | AGCATCCCTTTCAAA[C/T]GTTGTCAATGTCTAG | 51317 |
rs80048223 | snp | C/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46013476 | TGGGCCTCAGCTGAC[C/G]GTGAGTAACTAAAGC | 51317 |
rs80115758 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46036463 | CAAAATATTCACTGG[A/C]ATTTTGAAGAGAATT | 51317 |
rs80116517 | snp | C/T | 0.0279526 | 0.114869 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930300 | GCTGTGTGTAACCAC[C/T]TCCATGCACGCTGCC | 51317 |
rs80171383 | snp | A/G | 0.107694 | 0.205546 | intron-variant | PHF21A | GRCh38.p7 | 11:46063126 | GAATAGAGACGAAGA[A/G]AATAAAAAATAAAAG | 51317 |
rs80186421 | snp | A/C | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45998533 | CTTTTTTTTTTTTAA[A/C]CAGAGTTTTGCTCTT | 51317 |
rs80191689 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | PHF21A | GRCh38.p7 | 11:46031147 | AGTCACTTATCATTC[A/T]TTCTTCCTCTACCTT | 51317 |
rs80200623 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46084696 | TTTTTTTTTTTTTTT[G/T]TGAGATGGAGTCTCG | 51317 |
rs80237245 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46049857 | TCCTAAAAACAACGT[A/T]AAGACTATCCAGCAA | 51317 |
rs80250879 | snp | A/G | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45985167 | ACTTACTCAAAGAGG[A/G]AAAAAAAGACTTTCT | 51317 |
rs80258511 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46024892 | CCCTTTTCTATACCA[C/T]AGTGACTCCTAGTTC | 51317 |
rs80265661 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | PHF21A | GRCh38.p7 | 11:46118730 | AGAAGAAGAGAATAA[C/G]AAGGAACTTACCAAA | 51317 |
rs80297594 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:45936330 | AGAAGTTTTCCACTT[C/T]ATCCAATAAAAAGTT | 51317 |
rs80303343 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46036466 | AATATTCACTGGAAT[A/T]TTGAAGAGAATTATA | 51317 |
rs80319940 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | PHF21A | GRCh38.p7 | 11:46043168 | GTAAGAAATTCAATC[A/G]ATGTAAAGTACACTT | 51317 |
rs80355554 | snp | C/T | 0.0154538 | 0.0865337 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PHF21A | GRCh38.p7 | 11:45933232 | AACCACGGAGATGCG[C/T]GACTCACCAAGCAGG | 51317 |
rs111324568 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | PHF21A | GRCh38.p7 | 11:45952949 | TTTATCAGGGTCTTC[C/T]TTGCTATTTATGTTT | 51317 |
rs111338746 | snp | C/T | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46069603 | TAAAGGCAATGTAAT[C/T]ATTTTGCCTAATGTC | 51317 |
rs111389305 | snp | A/G | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46055200 | TTATCCCATTCTGTT[A/G]TAGATCTCTTACCCA | 51317 |
rs111402985 | snp | C/T | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46003182 | AGATTATTTCTTGCT[C/T]TGAAAAGAAAATCTG | 51317 |
rs111420443 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45936367 | TGCTTTGTTTCCTCC[A/C]ATAGTTAAGGGCAAA | 51317 |
rs111442351 | snp | A/G | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46003665 | ATATATTATGTAGAA[A/G]AGAAGTAAAGATGGA | 51317 |
rs111445192 | snp | A/G | 1.79419e-05 | 0.0029951 | intron-variant | PHF21A | GRCh38.p7 | 11:45971409 | GGACACTAAATCTAA[A/G]CTAAATAATAAACTA | 51317 |
rs111491626 | snp | A/T | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45940661 | TTCCTTCATTATTAA[A/T]ATCAGGCTGAGGGCT | 51317 |
rs111501765 | snp | G/T | 0.0166325 | 0.0896639 | intron-variant | PHF21A | GRCh38.p7 | 11:45935502 | GATGGCAAACTGCAT[G/T]TGCCCAAGTTAATCA | 51317 |
rs111511348 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46110878 | GCAACCTCCGCCTTC[C/T]GGGTTCAAGCGATTC | 51317 |
rs111551282 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46027500 | AAAACAGTACTACCT[A/G]CACCTGAATGCAGAT | 51317 |
rs111570922 | snp | A/C | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46075166 | CAGTAAGGTCCCTAA[A/C]AGAAAAAAGATTAAA | 51317 |
rs111573984 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | PHF21A | GRCh38.p7 | 11:46090764 | CCTGAATAACAACCT[C/G]TCAGGGATCTAGAAG | 51317 |
rs111608645 | snp | C/T | 0.0379877 | 0.132479 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46084836 | AGGCACCTGCCACTA[C/T]GCCCGGCTCATTTTT | 51317 |
rs111638742 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | PHF21A | GRCh38.p7 | 11:46000657 | GGGCATGGTGTCTCA[C/T]GTCTGTAATCCCAGT | 51317 |
rs111664751 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | PHF21A | GRCh38.p7 | 11:46103161 | ACTGATTTTCAAAAT[A/T]GTATAATTCTTTAAC | 51317 |
rs111666298 | snp | A/G | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46081974 | ACTATTCTCCATTCC[A/G]TATGGAGTAAATACC | 51317 |
rs111685229 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46029503 | GACCAGCCTGGGCAA[A/C]ATGGTGAAACCCTGT | 51317 |
rs111737788 | snp | G/T | 0.0360663 | 0.129354 | intron-variant | PHF21A | GRCh38.p7 | 11:45987513 | AAAAATACAAAAAAT[G/T]AGCTGGGCATAGTGG | 51317 |
rs111757512 | in-del | -/T | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45940199 | ATTTTAATCTTTTTC[-/T]TTTTTTTTTTTTTAG | 51317 |
rs111769395 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45956141 | AGGACATTCACTGCT[A/G]GTATACCAGTTCTAA | 51317 |
rs111784314 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46112325 | GAGGAAAAAAATGTG[A/G]AGCGTGCTATTTTTT | 51317 |
rs111868856 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | PHF21A | GRCh38.p7 | 11:45998507 | GCAAAATAACTCTAC[C/T]ATTTCTTTTTCTTTT | 51317 |
rs111899188 | snp | C/T | 0.089084 | 0.191327 | intron-variant | PHF21A | GRCh38.p7 | 11:46014966 | GCCTGGGCGACAGAG[C/T]GAGACTCCGTCTCAA | 51317 |
rs112026260 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | PHF21A | GRCh38.p7 | 11:46079753 | AAACTCTATCTAACT[C/T]GATTCCTCTGGGAAA | 51317 |
rs112057384 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46045317 | TAGCACACATTATTA[C/T]ACCAGGTACTAACAC | 51317 |
rs112057727 | snp | A/G | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45931512 | GGCCTGTTCAGCCTA[A/G]CTTAATTCCTTCTTC | 51317 |
rs112116511 | snp | C/G | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46056938 | TATCTATTTTTAAAA[C/G]TAATCAAGTACCTCA | 51317 |
rs112116826 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | PHF21A | GRCh38.p7 | 11:46089417 | ATTAACATGAATCAA[A/T]ACAAATGACAACATT | 51317 |
rs112167382 | snp | A/T | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45971586 | GTTCTCATATTGGTG[A/T]CACTTGTAAATGGGT | 51317 |
rs112167622 | snp | C/T | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45936894 | CCACCAACACAAAAG[C/T]TGCACATCAGCATGA | 51317 |
rs112223367 | snp | C/G | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45947833 | GTTACTGTGGCCCAG[C/G]AATCAATATAAAGCC | 51317 |
rs112232403 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:45978476 | TTCTTATAAAAAATT[C/T]ATTCTTTACTTGCAA | 51317 |
rs112296265 | snp | A/G | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45974714 | CACATCGGCCTCCCA[A/G]AGTGTTGGGATTACA | 51317 |
rs112357074 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:45966725 | CCCAGGTTCAAGTGA[C/T]TCTCCTGCCCCAGCC | 51317 |
rs112408785 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46110864 | AACCGCAGCTCACTG[C/T]AACCTCCGCCTTCTG | 51317 |
rs112456445 | in-del | -/A/AA/AAA | 0.597647 | 0.104683 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46119111 | GTGCACAACTGCTTT[-/A/AA/AAA]AAAAAAAAAAAACTT | 51317 |
rs112487202 | snp | A/G | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46022434 | CACTCCAGCCTGGGC[A/G]ACAAAGTGAGACCCT | 51317 |
rs112488690 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45988540 | TTGATGCTTAAAATC[A/G]TAATTTAAAAAATCA | 51317 |
rs112531721 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | PHF21A | GRCh38.p7 | 11:45995465 | GACAGTTATACTGTC[A/G]TAATTTTAGATGGTT | 51317 |
rs112534378 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:45998613 | CACCTCCCAGGTTCA[A/G]GTGATTCTCCTGCCT | 51317 |
rs112575725 | snp | A/G | 0.272241 | 0.249009 | intron-variant | PHF21A | GRCh38.p7 | 11:46110889 | CTTCTGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 51317 |
rs112671518 | snp | A/C | | | downstream-variant-500B, utr-variant-3-prime, missense | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45928862 | GCTGGGCCGGCGCTG[A/C]CCCTCATCTTAGCAT | 51317 |
rs112672168 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:45946407 | TTTATTTTTTGAGAC[A/G]GAATCTCGCTCTGTC | 51317 |
rs112674014 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | PHF21A | GRCh38.p7 | 11:45961915 | CTTGTTTTCTCAGAG[A/C]CACAGTGTAACGTGG | 51317 |
rs112698604 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PHF21A | GRCh38.p7 | 11:46059943 | AGATGGGGTTTCGCC[A/G]ATGTTGGCCAGCCTG | 51317 |
rs112719207 | snp | A/G | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46114105 | CACACACACACACAC[A/G]CACACATCCCCACAC | 51317 |
rs112782705 | snp | A/G | 1.64855e-05 | 0.00287097 | synonymous-codon, missense, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45934142 | GATGCCGTGGATGAG[A/G]CGAATCAGCTGTTTT | 51317 |
rs112787735 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45976537 | ACCACATAGATTGGT[A/G]GTACCAATAAATAGG | 51317 |
rs112936726 | snp | A/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46063839 | TCATCTGATGAACCC[A/T]CATCATAGGATAAGC | 51317 |
rs112947858 | snp | A/C | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45999757 | AGCACAGAGATGATA[A/C]GGGACTGATACCTAC | 51317 |
rs112965882 | in-del | -/T | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45983506 | AAAAAAAAAAATTTT[-/T]AAATCAAGATTTTGA | 51317 |
rs112972660 | snp | A/G | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46081131 | TGTATCACTTCAGAC[A/G]TTTATTCTAATTAAT | 51317 |
rs113075741 | snp | G/T | 0.5 | 0 | upstream-variant-2KB | PHF21A, LOC105376661 | GRCh38.p7 | 11:46123337 | GCAAAATTAAGTTTA[G/T]TTTCTCAAGAAAAAG | 51317 |
rs113103793 | snp | C/T | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46017754 | TGATAAATATGTAGA[C/T]TGATAGGAAAAACTA | 51317 |
rs113110426 | snp | C/T | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45938054 | AGCCCGGAGACGGAC[C/T]GGGAGAGAGAAGAGA | 51317 |
rs113118524 | snp | A/G | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46092458 | TTTTTCAAGACAAGC[A/G]AAAGTAAGTAGTTGA | 51317 |
rs113121420 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46117392 | AGCTATATTCATCTT[C/T]ATGCAGTTACTGTTA | 51317 |
rs113215157 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46044167 | AAATAATAGCAACTA[A/T]TAACACAAGACACAG | 51317 |
rs113249459 | snp | A/C | 0.0360663 | 0.129354 | intron-variant | PHF21A | GRCh38.p7 | 11:45966858 | TTCTGACCTCGGGAT[A/C]CACCCGCCTTGGCCT | 51317 |
rs113287708 | snp | A/T | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46024352 | GCCTCCTTTCTCCCA[A/T]GAAAGTGCTTTCTGC | 51317 |
rs113392556 | snp | C/T | 0.00557542 | 0.0525036 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45929609 | TGGGCTGAGGACCCA[C/T]GGACACCGGAGAGAG | 51317 |
rs113403366 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:46111012 | CTGGTCTCGAACTCT[C/T]GACCTCAGGTGATCC | 51317 |
rs113452869 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | PHF21A | GRCh38.p7 | 11:46091684 | CCATCAAATAGAACA[C/G]CATATTAAGTAACAC | 51317 |
rs113460975 | snp | A/G | | | intron-variant | PHF21A | GRCh38.p7 | 11:46014849 | GCTGGGCGTAGTGGC[A/G]GGCGCCTGTAGTCCC | 51317 |
rs113638559 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | PHF21A | GRCh38.p7 | 11:45999277 | ATATATTTTGTGCAA[C/T]GCTAACTCAAGGAAA | 51317 |
rs113638767 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | PHF21A | GRCh38.p7 | 11:46077013 | TACAGGCTCCTTGCA[C/T]CAAAACAGGAGCAGC | 51317 |
rs113642312 | snp | C/T | 0 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45962749 | ATACAAAAAATTAGC[C/T]GGGCATGGTGGCAGG | 51317 |
rs113691840 | in-del | -/G | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46016969 | AAAAATGTTTAACCT[-/G]GATTTTTTTTTTTTT | 51317 |
rs113692432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46043979 | TTTAATTTGTAGTAA[A/G]TCAAACAAACTGAGG | 51317 |
rs113832407 | snp | A/G | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45953919 | TAAGTATAGAAATAC[A/G]GTACAGGTTGTCCTT | 51317 |
rs113839797 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | PHF21A | GRCh38.p7 | 11:46019904 | CATATGCTTAACTTT[C/T]AGGGTTCCTAATAAT | 51317 |
rs113856535 | in-del | -/CC | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:45944476 | CTCCTCTGCCCAAAA[-/CC]CCCTGTAATGGTCTC | 51317 |
rs113857742 | snp | G/T | 0.0581099 | 0.160244 | intron-variant, utr-variant-5-prime | PHF21A | GRCh38.p7 | 11:46075101 | CAGAGAACAATTAGA[G/T]CTTGCCACTTGATGA | 51317 |
rs113886443 | snp | G/T | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46013585 | ACACAGTCATGTGTT[G/T]CTTAATAACAGGGAT | 51317 |
rs113933655 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46117834 | AATCCTTATACTATC[C/T]GCAATCGCACATCTA | 51317 |
rs113965618 | snp | A/C | 0.5 | 0 | intron-variant | PHF21A | GRCh38.p7 | 11:46089054 | GACACAGTGTGCCCC[A/C]AACTGTCCCTAAAAA | 51317 |
rs113981588 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46103797 | CGTTCAGATCCTGAT[C/T]AGTAGTGAATGAACA | 51317 |
rs114029809 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46007696 | ATATTAAATCCGTCA[C/T]TTTAAAATTTAGTTA | 51317 |
rs114036447 | snp | A/C | 0.0240643 | 0.107019 | intron-variant | PHF21A | GRCh38.p7 | 11:46002773 | CCCCCTCAAACCCCT[A/C]CACAGAACTAGTTTT | 51317 |
rs114042095 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46030893 | AGCAATTTCTACTTT[C/T]TGGGGGAAGTGGAGG | 51317 |
rs114063341 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:45940714 | GCCTTTCTTGAACCT[C/T]ATCCCTAAGTGGTGA | 51317 |
rs114068184 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | PHF21A | GRCh38.p7 | 11:45992036 | GCAGGCCAGGTGTAA[C/G]ATACTAGGCATGATA | 51317 |
rs114195657 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | PHF21A | GRCh38.p7 | 11:46018658 | ACATATGTCACATGA[C/T]TTGGCAAAAGATAAT | 51317 |
rs114200229 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PHF21A | GRCh38.p7 | 11:46105043 | GTCAGGCACTTCTAC[C/T]AGTTTACACATTAAC | 51317 |
rs114235380 | snp | C/T | 0.0166325 | 0.0896639 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45933490 | CTTTTTTTGGTTTTA[C/T]AGTAGCGAAAGTTTA | 51317 |
rs114289623 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | PHF21A | GRCh38.p7 | 11:45959987 | CATCAACACTACTTT[A/G]CACCCACTGAAATGG | 51317 |
rs114306048 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | PHF21A | GRCh38.p7 | 11:45944045 | AAACAGACAATATCA[C/T]GACAATAAATGTCAA | 51317 |
rs114366237 | snp | A/T | 0.0869089 | 0.189476 | intron-variant | PHF21A | GRCh38.p7 | 11:45982429 | AAAGTCTTTGCAGAA[A/T]CTATCTGCAGAATAA | 51317 |
rs114438715 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PHF21A | GRCh38.p7 | 11:46072144 | ACAGATACAGATATG[C/T]TACTGTAATAGAAAA | 51317 |
rs114440675 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PHF21A | GRCh38.p7 | 11:45984601 | GTTCGTTTTTCCACC[A/G]TTTAAGTCACGTTCC | 51317 |
rs114456090 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PHF21A | GRCh38.p7 | 11:45978024 | CAGAGATGGTGGGCC[A/G]GTTGCGGTGGCTCAC | 51317 |
rs114487573 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PHF21A | GRCh38.p7 | 11:46056150 | GTAATTTAATGCCTC[C/T]GGTTTTGAATTTCAT | 51317 |
rs114582398 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:45972111 | TGGAGAACTGCTGCA[C/G]AAGTGATCAAAGATG | 51317 |
rs114691332 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:46062340 | TTTTATTAGCCAGGC[A/C]TGAGACTTTCTGGGT | 51317 |
rs114707204 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PHF21A | GRCh38.p7 | 11:46001938 | TAAGGCAGAGTTAGC[A/G]CTACTTCATAAAAAC | 51317 |
rs114728305 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | PHF21A | GRCh38.p7 | 11:46119409 | GACATCATTTTAAAA[A/G]CAACACAATGTGGAC | 51317 |
rs114873973 | snp | A/T | 0.0513262 | 0.151752 | intron-variant | PHF21A | GRCh38.p7 | 11:46118563 | ACAGAAATTTTTTTA[A/T]AAACATTAGCATAAC | 51317 |
rs114911658 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46002351 | TAGTCCTCAAAATAT[C/T]TGTGGAATGGCTAAT | 51317 |
rs114914523 | snp | C/T | 0.0410537 | 0.137264 | utr-variant-3-prime, nc-transcript-variant | PHF21A | GRCh38.p7 | 11:45930871 | GTGGCTGGGGTGGGG[C/T]AGTGTCACGAGCGTA | 51317 |
rs114940648 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PHF21A | GRCh38.p7 | 11:46071908 | AAAAGCAAGACACAC[C/T]GTTCTATAAAAAAAT | 51317 |
rs114947121 | snp | C/T | 0.030278 | 0.119257 | intron-variant | PHF21A | GRCh38.p7 | 11:46053441 | CAAAGTTGCTGGGCC[C/T]AAATATTAAGTATAA | 51317 |
rs115032202 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PHF21A | GRCh38.p7 | 11:46103190 | ACTCAACCCCCAAAC[A/G]CTTGTAGAATCTCTT | 51317 |
rs115122121 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:45949232 | AAAAAAACCTAAGGG[A/G]TAAGCAGTGACTAAT | 51317 |
rs115139565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:45942813 | AGTAGGTTCTGAGAA[C/T]CTTCAAGTTCAAGGG | 51317 |
rs115266127 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF21A | GRCh38.p7 | 11:46000102 | CTTTTAACTGCTTGA[C/T]AGGTGTAAGCAAAAT | 51317 |
rs115272611 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PHF21A | GRCh38.p7 | 11:45944041 | TACCAAACAGACAAT[A/G]TCATGACAATAAATG | 51317 |
rs115283071 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | PHF21A | GRCh38.p7 | 11:45938665 | TAAGAGATTAACAAC[A/T]GTGACTAAGAAAACA | 51317 |
rs115286836 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:45977802 | CCTTCTTTGGTTTTA[C/T]ACAGTATTGGTATTG | 51317 |
rs115303644 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46013215 | ATAATAATGTGAGAT[A/G]AGTGGCATAGGCACT | 51317 |
rs115337886 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | PHF21A | GRCh38.p7 | 11:45936732 | TTCTGGACTAAAAAG[C/T]TCCAAATATCAGCTT | 51317 |
rs115337894 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PHF21A | GRCh38.p7 | 11:46016615 | ATTCAAAGAGCACCC[A/G]TGTACAACTTTAAAA | 51317 |
rs115380303 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:46051688 | GGAAGAGAATGGTCA[C/T]CATGCCTCAACTCAA | 51317 |
rs115502826 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PHF21A | GRCh38.p7 | 11:46043539 | ACTGGCCTAGTGAAG[C/T]TTTGGCCCCTGAAGT | 51317 |
rs115509848 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46055239 | AAAGCAGCAAATTTT[C/T]AGTAATTTTTTTTAT | 51317 |
rs115531190 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:45992232 | AAAGTGGAATTAGAC[A/G]TTACTTAGAAAATTT | 51317 |
rs115574237 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PHF21A | GRCh38.p7 | 11:46009409 | TATAAAACTTTTCTT[A/G]ACTCTACCTGCCTAG | 51317 |
rs115659933 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PHF21A | GRCh38.p7 | 11:45977200 | CATGGAGTGCAGTAC[A/G]ATCTCGGCTCACTGG | 51317 |
rs115666620 | snp | A/C | 0.0244538 | 0.107838 | intron-variant | PHF21A | GRCh38.p7 | 11:45969406 | CATCACTTTCCAGGG[A/C]AGAACTGAAGAATAG | 51317 |
rs115749090 | snp | G/T | 0.0599851 | 0.162463 | intron-variant | PHF21A | GRCh38.p7 | 11:46034801 | TGACCCAGTTTCCCA[G/T]GATATAGTGATTGGT | 51317 |
rs115762768 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | PHF21A | GRCh38.p7 | 11:46021216 | AGGTGCAAGCCGCTA[G/T]GCCTGGCTAATTTTT | 51317 |
rs115834545 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | PHF21A | GRCh38.p7 | 11:45974825 | GTATGATCACCTTTA[A/G]GAGAAGGTAGCTGTT | 51317 |
rs116041698 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:45948490 | ACACTCTGGCCTTGC[C/T]GGCAGCAGGACAACC | 51317 |
rs116135958 | snp | A/C | | | intron-variant | PHF21A | GRCh38.p7 | 11:46067598 | ATATTCCACCCCCCA[A/C]AAAAAAAAAAAAAAC | 51317 |
rs116140393 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | PHF21A | GRCh38.p7 | 11:45942800 | GGGGTGTGCCACTAG[C/T]AGGTTCTGAGAACCT | 51317 |
rs116196180 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PHF21A | GRCh38.p7 | 11:46002822 | CTTCTTCCCCAAGGC[C/T]GAAATTTGTAATGAA | 51317 |
rs116234578 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | PHF21A | GRCh38.p7 | 11:45946837 | TGAGGGTGGAGACCG[A/G]CAAAGCAAGGAGGCA | 51317 |
rs116297205 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46014191 | TTGTGGAGTCCCTAG[G/T]GTTTACTGTTCCCAT | 51317 |
rs116390602 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:46029824 | TTAAAAGTATTTCAA[C/T]TTTACTCCACCTGCA | 51317 |
rs116402195 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PHF21A | GRCh38.p7 | 11:46061583 | AATTCTTTCCCATAC[C/T]TTCCAAAGAAACTAT | 51317 |
rs116406714 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:45981510 | TCATAAAGCATATAA[C/T]AACTATTTGGGGCCA | 51317 |
rs116435225 | snp | A/C | 0.0244538 | 0.107838 | intron-variant | PHF21A | GRCh38.p7 | 11:46002774 | CCCCTCAAACCCCTC[A/C]ACAGAACTAGTTTTA | 51317 |
rs116455470 | snp | C/G | 0.0244538 | 0.107838 | intron-variant | PHF21A | GRCh38.p7 | 11:46013636 | TTAGGTCATTTCATT[C/G]CTGTGCGAACATCAT | 51317 |
rs116491232 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PHF21A | GRCh38.p7 | 11:46013656 | GCGAACATCATACAA[C/T]GTACTTAAACAAACT | 51317 |
rs116511920 | snp | C/T | 0.0581099 | 0.160244 | intron-variant | PHF21A | GRCh38.p7 | 11:46083293 | ATTTCTGAACAGGTG[C/T]TTTTGAAGCTTCCTT | 51317 |
rs116512051 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | PHF21A | GRCh38.p7 | 11:46007255 | AGGAATCCAGGTAGC[A/G]CTGAAGCCAGGAATC | 51317 |
rs116598319 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | PHF21A | GRCh38.p7 | 11:46002457 | ATCTCTTTCCATTTA[C/T]AAATGATGATTTATT | 51317 |
rs116606624 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PHF21A | GRCh38.p7 | 11:46098832 | TAATGGGAGTTCTGG[A/G]TGTAAACCATAAGCA | 51317 |
rs116607064 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:46024141 | TAATGATTTTATATG[C/T]TGGGCTAACTGAGTT | 51317 |
rs116636593 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | PHF21A | GRCh38.p7 | 11:45943461 | TTGGGATTTACAGGC[A/G]TGAGCCACCGTGCCT | 51317 |
rs116710419 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | PHF21A | GRCh38.p7 | 11:45958672 | TATAATCCCAACACT[C/T]TGGGAAGCCAAGGTC | 51317 |
rs116765832 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | PHF21A | GRCh38.p7 | 11:46097163 | TGGCCTCCCCAATTC[G/T]ACCCTAGCCCCGCTA | 51317 |
rs116797847 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | PHF21A | GRCh38.p7 | 11:45964991 | GAAACTAACATGGCG[C/T]TTTCTGTTTACTACC | 51317 |
rs116876530 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | PHF21A | GRCh38.p7 | 11:46102189 | CCTGAGCTCAAGTGA[C/T]ACACCAGCCTCGGCC | 51317 |
rs116914034 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | PHF21A | GRCh38.p7 | 11:46080958 | CGTAAGCCACCATGC[A/G]CAGCTCTTGCTACTA | 51317 |
rs117006850 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:46044428 | CACTTCCAGTGACCC[C/T]GGTACTACTTTTTCC | 51317 |
rs117054998 | snp | A/G | 0.00360956 | 0.0423291 | intron-variant | PHF21A | GRCh38.p7 | 11:45950166 | AGGAACAAAGCTGTG[A/G]GCCAGAAAAAAAGGC | 51317 |
rs117070297 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | PHF21A | GRCh38.p7 | 11:46013159 | TGGGATTGATGGGTA[A/T]GAGATTAACAACACC | 51317 |
rs117102163 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PHF21A | GRCh38.p7 | 11:46079885 | AAAGAGGAAAGGAAA[A/G]GAAAAGAAAGGAAAG | 51317 |
rs117109731 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | PHF21A | GRCh38.p7 | 11:45958132 | ATCAAAATTCTCCCC[A/G]AAAAGAAAAAGTACA | 51317 |
rs117110449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46027782 | TTAAACAATGATTTA[C/T]ATCTTCTTTTTATCC | 51317 |
rs117116727 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | PHF21A | GRCh38.p7 | 11:45955994 | CAGAACTAAGTTGCA[A/G]ACCAGAAGGAAATGG | 51317 |
rs117140398 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | PHF21A | GRCh38.p7 | 11:46050572 | AGCATCTCTGGGAGG[A/G]GAATGAAGTAGGTAC | 51317 |
rs117160929 | snp | A/T | 0.0482946 | 0.147699 | intron-variant | PHF21A | GRCh38.p7 | 11:46032842 | CCATTAATGATTTTA[A/T]TATGTTTAATGATTC | 51317 |
rs117161050 | snp | C/T | | | intron-variant | PHF21A | GRCh38.p7 | 11:45957227 | AAGTAATGGATAAAA[C/T]TTGTGCAGAGATTAA | 51317 |
rs117167419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46005475 | TAAGAAAAGCAAAAA[C/T]CTCATTTGCAATATT | 51317 |
rs117174409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46110376 | GCCTGGGGCATTTCA[C/T]TAAAAAAGAAAACTG | 51317 |
rs117234885 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46014313 | GATAATGGCCTCCAG[C/T]TGCAGCCATGTTGCT | 51317 |
rs117243792 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PHF21A | GRCh38.p7 | 11:46019669 | CTTAAGCAATCAGAC[A/G]GCATTCCAATCTTAG | 51317 |
rs117263461 | snp | A/T | 0.0547386 | 0.156121 | downstream-variant-500B, utr-variant-3-prime, missense | PHF21A, LARGE2, GYLTL1B | GRCh38.p7 | 11:45928877 | CCCCTCATCTTAGCA[A/T]TGGGCAGACACCAGG | 51317 |
rs117278384 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | PHF21A | GRCh38.p7 | 11:45935302 | CAGTGTCAGGTGAGG[C/T]GCTACACTCCCCCCA | 51317 |
rs117289621 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PHF21A | GRCh38.p7 | 11:46030282 | GGTGTCAAGACAATA[C/T]AAAATTATTTTTTCT | 51317 |
rs117320749 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | PHF21A | GRCh38.p7 | 11:46060302 | TACACCCCAACCATG[A/T]ATTACTTTTATAAAC | 51317 |
rs117323370 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | PHF21A | GRCh38.p7 | 11:46112975 | TAAGGTAAACTAAAA[C/G]ACTAGGTTGTTTCTG | 51317 |
rs117335563 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | PHF21A | GRCh38.p7 | 11:46058206 | GGTTAAACTGCTAAT[A/G]TTCTTAGATGTCAAG | 51317 |
rs117363356 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:45997499 | CCAGCCCATGCCTAC[A/G]TGAAACAGCTCCTGA | 51317 |
rs117478001 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PHF21A | GRCh38.p7 | 11:45936208 | GACTGGGCCCAGGAG[A/G]AGGAAGCTGCAGTGG | 51317 |
rs117496034 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | PHF21A | GRCh38.p7 | 11:46066218 | GAGGAGGTAGTGAAC[C/T]GGGGAAGGACGAAGG | 51317 |
rs117499746 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:45993822 | GCTGGGAAACGGGAC[G/T]GTCAGAGATGAGGCT | 51317 |
rs117500352 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | PHF21A | GRCh38.p7 | 11:46059174 | AATTACGTACAAATA[C/T]TTACGTCCAAGGATG | 51317 |
rs117594625 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF21A | GRCh38.p7 | 11:45980197 | GCAACTGAGGCACAC[A/G]AATGAAAAATCTGAA | 51317 |
rs117648251 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:45949136 | CTCTCAGAGAAGCCT[G/T]CCTCTGTTGCCGATG | 51317 |
rs117675627 | snp | A/T | 0.0189856 | 0.0955633 | intron-variant | PHF21A | GRCh38.p7 | 11:45949629 | AGCAGAGGCAAGCAC[A/T]CTACTGGAAGCAAAT | 51317 |
rs117698574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46002039 | TGAGAAAATATAAAG[A/G]AAAGAGTGACTATTT | 51317 |
rs117706643 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PHF21A | GRCh38.p7 | 11:45967130 | TCCCAACAATTCGGG[A/G]GGCTGAGGCTGGTGG | 51317 |
rs117711927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF21A | GRCh38.p7 | 11:46009698 | CAGAGCCAGAGCAGA[C/T]TTCCAACTTGGGCAG | 51317 |
rs117798677 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46087634 | AATTACAGACATGTA[C/T]TTATAGTTTACAAAA | 51317 |
rs117847116 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | PHF21A | GRCh38.p7 | 11:46026689 | TATGAGCAGAGCTCC[C/T]GTGGGCTTTTAAATC | 51317 |
rs117850541 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | PHF21A | GRCh38.p7 | 11:46079363 | AAAAAAATCAAACCA[C/T]CACTTTATATTTGAA | 51317 |
rs117929980 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | PHF21A | GRCh38.p7 | 11:46022224 | TTGGGAGGCCAAGGT[C/G]GGAGGACCACTTGAG | 51317 |
rs117958458 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | PHF21A | GRCh38.p7 | 11:45980236 | CACAGCAGAGCTCAG[A/G]TGTCCTATTATTAAC | 51317 |
rs118044321 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF21A | GRCh38.p7 | 11:45968443 | TGTGCTCAGCCACAG[C/T]AAACCTCCTTTGGTT | 51317 |
rs118047297 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF21A | GRCh38.p7 | 11:46049284 | TTTCTCAAATCCTGA[G/T]AGTAAGGTATGTTGT | 51317 |
rs118078746 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PHF21A | GRCh38.p7 | 11:45933125 | CTGATCCACCTTTTT[C/T]TCCTTCCTGGACACA | 51317 |
rs118097121 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | PHF21A | GRCh38.p7 | 11:45946955 | ATGCTCTGGGCTTAG[C/T]AATTAATGTTTAAGT | 51317 |
rs118115357 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | PHF21A | GRCh38.p7 | 11:45938457 | AGCAGGAATCACCAA[C/T]AGCACATGCCCCTAC | 51317 |
rs118152342 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PHF21A | GRCh38.p7 | 11:45973436 | GCCTTATGCGCATAT[A/C]CACATATTATCTAAT | 51317 |
rs118162057 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | PHF21A | GRCh38.p7 | 11:46074321 | TTCTTCAAACTTTTC[C/T]GTATTTTAAATTTTT | 51317 |
rs137925093 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | PHF21A | GRCh38.p7 | 11:45957912 | AATAAGAAGATACAA[A/G]TAACTAAAACCAAAA | 51317 |