| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs5951419 | snp | A/G | 0.0292288 | 0.117303 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22270936 | TGTTGCGTTTTCACC[A/G]TTAGTGAAGTCAAGA | 158506 |
| rs5951426 | snp | G/T | 0.356985 | 0.225952 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273489 | CAGTCTTTTAGGGAT[G/T]TCAGAGATTTCAGTT | 158506 |
| rs5951547 | snp | C/T | 0.410964 | 0.191287 | downstream-variant-500B, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274682 | AATGTGAAATAATTA[C/T]CTACCATTTAGCTGT | 158506 |
| rs5951548 | snp | A/G | 0.464279 | 0.12878 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272415 | TGTGTGCATGTATAT[A/G]TACATACACACAAAA | 158506 |
| rs6528099 | snp | C/G | 0.0787474 | 0.182133 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22271034 | tggatcacctgaagt[C/G]aggagtttgagacca | 158506 |
| rs6528102 | snp | A/T | 0.489957 | 0.0701457 | downstream-variant-500B, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274484 | GGTTTTTATTTTTTT[A/T]TTTTTTGGTGATATG | 158506 |
| rs6629461 | snp | C/T | 0.310359 | 0.242604 | synonymous-codon, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273615 | GCCACATAAGGATAT[C/T]CAGGCTCCTCCCCCA | 158506 |
| rs6633535 | snp | G/T | 0 | 0 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272392 | CAAAATCTTAAAAGG[G/T]ATGTGTATTTTGTGT | 158506 |
| rs6633536 | snp | G/T | 0 | 0 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272474 | ATGAGTGATTTAAGG[G/T]AGTTCACAAAAATGC | 158506 |
| rs6633537 | snp | A/G | 0.340069 | 0.233211 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272766 | CACTTTCGCCTCCTA[A/G]GCTGGGGAAGATGGT | 158506 |
| rs7877302 | snp | C/T | 0.493176 | 0.0580107 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22271936 | AAATGTCTAGCCCAG[C/T]GAAGTTACCATCTAT | 158506 |
| rs7885426 | snp | C/T | 0.0560809 | 0.157783 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22271119 | gtgtggtggcacatg[C/T]ctatagtcccatcta | 158506 |
| rs12013449 | snp | C/T | 0.0261392 | 0.111294 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272513 | AAAAATAAGTCAGTC[C/T]TAGAAGGCAAAGCTC | 158506 |
| rs12556801 | snp | G/T | 0.29094 | 0.246625 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22271917 | AGAACAGCAAATGTC[G/T]AAAAAATGTCTAGCC | 158506 |
| rs12834209 | snp | A/C | 0.0266548 | 0.112325 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22270933 | CATTGTTGCGTTTTC[A/C]CCATTAGTGAAGTCA | 158506 |
| rs12834646 | snp | C/T | | | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22271076 | gtggtgaaaccccgt[C/T]tctactaaaaataca | 158506 |
| rs12834654 | snp | C/T | | | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22271078 | ggtgaaaccccgtct[C/T]tactaaaaatacaaa | 158506 |
| rs12843875 | snp | G/T | | | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22271961 | ATCTATTCACTCCTG[G/T]TTTTTTTTTTTTTTT | 158506 |
| rs12843876 | snp | G/T | | | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22271962 | TCTATTCACTCCTGT[G/T]TTTTTTTTttttttt | 158506 |
| rs12860105 | snp | C/T | 0.00394476 | 0.0442359 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273851 | ATGCGCCACCTCCAT[C/T]TCCATCATCACCAGT | 158506 |
| rs16981921 | snp | C/T | 0.0500702 | 0.150094 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22270926 | ATTGGGGCATTGTTG[C/T]GTTTTCACCATTAGT | 158506 |
| rs16981925 | snp | A/G | 0.0348667 | 0.127349 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22271823 | GTTGCTGTTTTTACG[A/G]TCCAGTTTGTACTTA | 158506 |
| rs34516956 | in-del | -/T | 0.483247 | 0.0899768 | downstream-variant-500B, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274925 | GTTACTTGTTAATGC[-/T]TTTTTTTTTTTTTTT | 158506 |
| rs56006398 | snp | G/T | 0.00158814 | 0.0281345 | utr-variant-3-prime, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274325 | AAAACCTTCAAGTTC[G/T]ATACTGTACTGTGGA | 158506 |
| rs57690843 | snp | C/G | | | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272268 | AGGAGTGAGCCAAGG[C/G]GCCTGACACTATTCA | 158506 |
| rs59090833 | snp | A/G/T | 0.00581083 | 0.0535878 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272107 | CCTGCCTCCTGAGTA[A/G/T]CTGAGATTACAGGCG | 158506 |
| rs73636821 | snp | C/T | 0.0245906 | 0.108123 | downstream-variant-500B, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274790 | AGAAGCACCAAAATA[C/T]ATCAGAATTCCAGTA | 158506 |
| rs75062800 | snp | A/G | 0.00618021 | 0.0552441 | synonymous-codon, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274158 | AATGGATCATAGAAG[A/G]TGGCCTGCATGGAAA | 158506 |
| rs111333157 | snp | A/G/T | 2.34775e-05 | 0.0034261 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274247 | CACATCATTCACACC[A/G/T]GAGAAGACATAGACG | 158506 |
| rs112059840 | snp | C/T | 0.128718 | 0.218611 | downstream-variant-500B, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274692 | GGTAGATAATTATTT[C/T]ACATTTTAGGAACTG | 158506 |
| rs112235331 | snp | A/C/G | 0.00385373 | 0.0437266 | synonymous-codon, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273636 | TCCTCCCCCAGAACT[A/C/G]TCTCTAAGTCTGCCT | 158506 |
| rs113181888 | snp | A/G | 0.5 | 0 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273298 | TATCCTGTGCTGAGA[A/G]TTGAGGCGCATAAAC | 158506 |
| rs113259855 | snp | C/T | 0 | 0 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272144 | ACCATGCCTAGCTAA[C/T]TCTTGTATTTTTAGT | 158506 |
| rs113314974 | snp | A/T | 0.00239573 | 0.0345271 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273530 | ACCATCTAAGCTATA[A/T]TCCACCAGAACAGCA | 158506 |
| rs138094158 | snp | A/G | 0.0033452 | 0.0407604 | synonymous-codon, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273825 | TCATATTATACCTCA[A/G]AAACAGCATTATGCG | 158506 |
| rs138176282 | snp | A/T | 0.0022018 | 0.0331067 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273089 | GAAAAAAGAAAAAAA[A/T]TCCTGGTTACCGTTG | 158506 |
| rs138673057 | snp | C/G | 0.000319019 | 0.0126257 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273925 | AACTCGGTTCGTAGC[C/G]AAGTGCCAGCTCTAA | 158506 |
| rs139423670 | snp | A/C | 0.0168099 | 0.0901243 | downstream-variant-500B, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274514 | GTTAACCTGTGTAAA[A/C]GGGTTAAATTTCAAT | 158506 |
| rs139621376 | snp | A/G | 0.0013226 | 0.0256817 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273452 | CGCTTGAAAAAGTTC[A/G]TCCTCATATTGCTCC | 158506 |
| rs140897254 | snp | C/G | 0.0389457 | 0.134 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272273 | TGAGCCAAGGCGCCT[C/G]ACACTATTCACTGCC | 158506 |
| rs140922897 | snp | A/T | 1.64727e-05 | 0.00286986 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274091 | TTAACATTTTACCTC[A/T]GTTCACCGAAAATCA | 158506 |
| rs141135903 | snp | A/G | 0.103655 | 0.20269 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272052 | CAGTGACGCGATCTC[A/G]GCTCACTGCAACCTC | 158506 |
| rs141246738 | snp | C/T | 0.00263281 | 0.0361866 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273743 | ACTCAGATTCTGGTG[C/T]TAAGAAGCCAACACC | 158506 |
| rs141295358 | snp | A/C | 0.0302564 | 0.119217 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272612 | TTGAGTACTGAAGAG[A/C]AGCATCAGCAACCTC | 158506 |
| rs141753613 | snp | G/T | 4.55809e-05 | 0.00477372 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273866 | CTCCATCATCACCAG[G/T]AAACCATCAAATGCC | 158506 |
| rs142294017 | snp | C/G | 0.000136924 | 0.00827304 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273340 | TTCATGTGTAGTATT[C/G]TTCAGCAGTGCAAGA | 158506 |
| rs142781082 | snp | C/G | 0.000189982 | 0.00974449 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273000 | AAGGAATATGAACAA[C/G]ATGCCTGCTGGTGAA | 158506 |
| rs142874640 | snp | C/T | 0.000251408 | 0.011209 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274193 | TGTCACCTTGTCCAC[C/T]AACGCGGAGTCCACC | 158506 |
| rs143029068 | snp | A/G | 4.57661e-05 | 0.0047834 | synonymous-codon, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273687 | CGTTAGTATTTTTAC[A/G]AGAAAACATGGCAAT | 158506 |
| rs144175358 | snp | C/T | 0.000189982 | 0.00974449 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273271 | GGATATAAAGTATGT[C/T]CGCGCTGTCGTTATC | 158506 |
| rs144353133 | snp | C/T | 0.00581083 | 0.0535878 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22271417 | TACTTAACAAGAATA[C/T]CACCTTCCCCATCAA | 158506 |
| rs144357703 | snp | A/G | 2.28128e-05 | 0.00337726 | synonymous-codon, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273468 | TCCTCATATTGCTCC[A/G]CCACAAACTGAAATC | 158506 |
| rs145057529 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272676 | CCCTCACTAGAGTGG[C/T]GGGACAGGGTAGGTG | 158506 |
| rs146303957 | snp | A/G/T | 0.000296252 | 0.0121677 | synonymous-codon, missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273981 | ATATATTATTGTAAA[A/G/T]GTGCCACCTGATATG | 158506 |
| rs146331121 | snp | C/T | 9.13096e-05 | 0.00675622 | stop-gained, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273415 | CGCCATAAGAGAGCT[C/T]GAAAACAAGTTACCA | 158506 |
| rs146611118 | snp | A/G | 2.28097e-05 | 0.00337703 | synonymous-codon, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273474 | TATTGCTCCGCCACA[A/G]ACTGAAATCTCTGAC | 158506 |
| rs146977013 | snp | A/C | 2.28136e-05 | 0.00337732 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273805 | CCAGCGGTATCGTCC[A/C]CTCATCATATTATAC | 158506 |
| rs147382653 | snp | C/T | 0.00235482 | 0.0342325 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274198 | CCTTGTCCACCAACG[C/T]GGAGTCCACCTCCTT | 158506 |
| rs147408051 | snp | A/G/T | 0.00113649 | 0.0238112 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273088 | AGAAAAAAGAAAAAA[A/G/T]TTCCTGGTTACCGTT | 158506 |
| rs147787234 | snp | C/T | 0.000114553 | 0.00756725 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273719 | TAACAGTTGATCATA[C/T]TCAGAATAACTCAGA | 158506 |
| rs148712606 | snp | A/G | 6.84611e-05 | 0.00585029 | synonymous-codon, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273273 | ATATAAAGTATGTCC[A/G]CGCTGTCGTTATCCT | 158506 |
| rs149337344 | snp | A/C | 0.00186705 | 0.0304965 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273926 | ACTCGGTTCGTAGCC[A/C]AGTGCCAGCTCTAAC | 158506 |
| rs149542720 | snp | C/T | 4.61782e-05 | 0.00480489 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273100 | AAAATTCCTGGTTAC[C/T]GTTGGGGGGACATTA | 158506 |
| rs150664878 | snp | A/C/G | 0.000114082 | 0.00755179 | synonymous-codon, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273801 | TCAACCAGCGGTATC[A/C/G]TCCCCTCATCATATT | 158506 |
| rs150907787 | snp | G/T | 0.0605624 | 0.163136 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22270962 | CAAGAGTCAACAACT[G/T]GGCCAGGCGCGGTGG | 158506 |
| rs151015591 | snp | C/T | 0.00633741 | 0.0559334 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272228 | ACGATCTGCCTGCCT[C/T]GGCCTTCCAAAGTGC | 158506 |
| rs180830452 | snp | C/G | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22271868 | TGTGAGGAAATGTGG[C/G]CTAAATACCCATAAC | 158506 |
| rs180904294 | snp | A/G | 0.000529661 | 0.016265 | downstream-variant-500B, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274544 | TACAGCTGTAAAAAT[A/G]CTATTTTATGTGAAC | 158506 |
| rs181036832 | snp | G/T | | | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272034 | GTCGCCCAGGCTGGA[G/T]TGCAGTGACGCGATC | 158506 |
| rs181797502 | snp | C/G | 0.00528398 | 0.051128 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22271707 | GGAGGGCACGGAGTA[C/G]GGGTTGACAGCCAAC | 158506 |
| rs183525998 | snp | A/G | 0.00105904 | 0.0229869 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272691 | TGGGACAGGGTAGGT[A/G]AGGAGAGAAGGAAGC | 158506 |
| rs183894704 | snp | A/G | 0.00633741 | 0.0559334 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22271109 | AATTAGCCAGGTGTG[A/G]TGGCACATGCCTATA | 158506 |
| rs184196652 | snp | C/T | 0.00105904 | 0.0229869 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22271550 | CCTGAAACCACCCAA[C/T]TTAGTCCCTAATAAC | 158506 |
| rs184448876 | snp | A/C | 0.00791544 | 0.0624105 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22271327 | TAATCCATGTTGAGA[A/C]TAAGCAAACTTAGCT | 158506 |
| rs184716539 | snp | A/T | 0.00105904 | 0.0229869 | downstream-variant-500B, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274482 | GTGGTTTTTATTTTT[A/T]TATTTTTTGGTGATA | 158506 |
| rs185237932 | snp | G/T | 0.00158814 | 0.0281345 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22271890 | ACCCATAACCCTTTT[G/T]AAAATTAAGCAAGAA | 158506 |
| rs185501024 | snp | C/G | 0.0287145 | 0.11633 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272124 | TGAGATTACAGGCGC[C/G]TGCCACCATGCCTAG | 158506 |
| rs185586921 | snp | C/G | 0.00158814 | 0.0281345 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22271734 | CAACGAAGCTAAAAG[C/G]GTGAATGTCTGCACA | 158506 |
| rs186622393 | snp | C/G | 2.29621e-05 | 0.00338829 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273138 | CATCATAGGTGAAAA[C/G]GATGATTTACCAATT | 158506 |
| rs187097397 | snp | A/C | 0.00317376 | 0.039709 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22271463 | TCTCCTCCTGCTATG[A/C]CCACCAATCTACAGC | 158506 |
| rs187258946 | snp | C/T | 2.28851e-05 | 0.00338261 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273563 | CCATGGTGTCACTAC[C/T]GTCTGTGCAACATAT | 158506 |
| rs187271405 | snp | C/T | 0.00475684 | 0.0485365 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272811 | ATGCGCACGTGTTAC[C/T]GGCACATGACTCCCG | 158506 |
| rs188835886 | snp | A/G | 0.00211696 | 0.0324653 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22271253 | TACTGAAACCAACAT[A/G]ATTCTCTGTCGCTGT | 158506 |
| rs188918118 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22271700 | TTTTAGGGGAGGGCA[C/T]GGAGTAGGGGTTGAC | 158506 |
| rs190500499 | snp | A/G | 0.00475684 | 0.0485365 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22271788 | ATTATGGGTGGAGTG[A/G]AGGCAGAAAAATATG | 158506 |
| rs190506241 | snp | A/G | 0.00158814 | 0.0281345 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22270927 | TTGGGGCATTGTTGC[A/G]TTTTCACCATTAGTG | 158506 |
| rs190603898 | snp | C/T | 0.000227884 | 0.0106719 | synonymous-codon, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274152 | AGATGCAATGGATCA[C/T]AGAAGGTGGCCTGCA | 158506 |
| rs191471321 | snp | A/G | 2.28217e-05 | 0.00337792 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273355 | GTTCAGCAGTGCAAG[A/G]GAACATACTTGTCTC | 158506 |
| rs191695581 | snp | C/G | | | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272652 | GCTTTTTCTTTCTCT[C/G]CCCAAATTCCCTCAC | 158506 |
| rs191904272 | snp | C/T | 0.00581083 | 0.0535878 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22271484 | AATCTACAGCTATTA[C/T]GTCACAAAATCTACC | 158506 |
| rs192067453 | snp | A/G | 0.000794774 | 0.0199187 | utr-variant-5-prime, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272972 | GACAAACCTAAATAT[A/G]TGTCTGAACTCCAAG | 158506 |
| rs192607182 | snp | C/T | | | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22271285 | TAAAACAATAACAGA[C/T]GTGGGAATAGTTTTC | 158506 |
| rs200078401 | snp | A/G | 0.000529661 | 0.016265 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273527 | GGGACCATCTAAGCT[A/G]TATTCCACCAGAACA | 158506 |
| rs200330462 | snp | A/C | | | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272537 | AAAGCTCTGCAGGGC[A/C]TGCTGGGAATTTATT | 158506 |
| rs200644599 | in-del | -/G | 0.0525796 | 0.153379 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22271141 | CCCATCTACTTGGAA[-/G]GGAAAAAAAAAAAAA | 158506 |
| rs200886998 | snp | C/G | 2.28264e-05 | 0.00337826 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273433 | AAACAAGTTACCAGC[C/G]CTTCGCTTGAAAAAG | 158506 |
| rs201219167 | in-del | -/A | | | downstream-variant-500B, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274484 | GGTTTTTATTTTTTT[-/A]TTTTTTGGTGATATG | 158506 |
| rs201362226 | in-del | -/G | | | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22271959 | CATCTATTCACTCCT[-/G]GTTTTTTTTTTTTTT | 158506 |
| rs201655784 | snp | A/G | 4.58432e-05 | 0.00478743 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273740 | ATAACTCAGATTCTG[A/G]TGCTAAGAAGCCAAC | 158506 |
| rs201682184 | snp | A/G | 6.83659e-05 | 0.00584622 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274102 | CCTCAGTTCACCGAA[A/G]ATCAAGAAACCTTGA | 158506 |
| rs201885236 | snp | C/T | 0.000296641 | 0.0121751 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273272 | GATATAAAGTATGTC[C/T]GCGCTGTCGTTATCC | 158506 |
| rs267606418 | snp | C/T | | | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273860 | CTCCATCTCCATCAT[C/T]ACCAGTAAACCATCA | 158506 |
| rs367998468 | snp | G/T | 2.27894e-05 | 0.00337553 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274034 | CCCAGTCTCAAAATG[G/T]TAATCCATCTGCAAG | 158506 |
| rs368209230 | snp | C/G | | | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272715 | AGGAAGCCCTTAAAC[C/G]TCAAAGCAGTGGAGG | 158506 |
| rs368787790 | snp | A/G | | | utr-variant-3-prime, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274336 | GTTCTATACTGTACT[A/G]TGGATAAGCGGCTCA | 158506 |
| rs369179285 | snp | C/T | 6.85526e-05 | 0.0058542 | synonymous-codon, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273222 | GTGCAAGCATGCTTT[C/T]TGCTATCACTGTGCT | 158506 |
| rs369622139 | snp | G/T | 2.43983e-05 | 0.00349264 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273024 | TGGTGAACAAGAATG[G/T]GAATATAACAAAGAA | 158506 |
| rs369818282 | snp | C/T | 2.32845e-05 | 0.003412 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274232 | CCCTACATGGTCGAT[C/T]ACATCATTCACACCA | 158506 |
| rs371087148 | snp | C/T | 0.000569599 | 0.0168664 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273839 | AGAAACAGCATTATG[C/T]GCCACCTCCATCTCC | 158506 |
| rs371413066 | snp | A/C | | | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272330 | TAAATGTAATGCTCC[A/C]TTCTTCCAGACAAAG | 158506 |
| rs371620931 | snp | C/T | 9.11546e-05 | 0.00675048 | synonymous-codon, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274074 | TTCTCACCATTATAA[C/T]CTTAACATTTTACCT | 158506 |
| rs371735626 | snp | A/G | 0.000137256 | 0.00828306 | synonymous-codon, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274197 | ACCTTGTCCACCAAC[A/G]CGGAGTCCACCTCCT | 158506 |
| rs371958882 | snp | A/C/G | 4.87936e-05 | 0.00493907 | utr-variant-3-prime, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274281 | TTAAGGATGATAACA[A/C/G]TATTTGGAACTGAAG | 158506 |
| rs372309067 | snp | C/T | 0.00475684 | 0.0485365 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272744 | GGGTTGGGGAGGCAT[C/T]GGATCGCACTTTCGC | 158506 |
| rs373087492 | snp | C/T | 2.28305e-05 | 0.00337857 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273400 | GCTCATATCAAACGC[C/T]GCCATAAGAGAGCTC | 158506 |
| rs373130793 | snp | A/T | 4.76207e-05 | 0.00487935 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273057 | GAAGTACTACTCTAA[A/T]GGAGTTAAACTGGTG | 158506 |
| rs373418646 | snp | A/G | 0.00105904 | 0.0229869 | utr-variant-3-prime, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274408 | TGGTAAATTGACCTA[A/G]AGGTGACCTCTGACG | 158506 |
| rs373551031 | snp | A/G | | | downstream-variant-500B, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274789 | CAGAAGCACCAAAAT[A/G]TATCAGAATTCCAGT | 158506 |
| rs374682719 | snp | A/G | 0.000189982 | 0.00974449 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273754 | GGTGCTAAGAAGCCA[A/G]CACCTCCCGACTATT | 158506 |
| rs375380699 | snp | A/G | 2.47798e-05 | 0.00351984 | utr-variant-5-prime, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272985 | ATGTGTCTGAACTCC[A/G]AGGAATATGAACAAG | 158506 |
| rs375492917 | snp | C/T | 2.27925e-05 | 0.00337576 | synonymous-codon, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273963 | CTACGATCCATCATC[C/T]GGATATATTATTGTA | 158506 |
| rs375566609 | snp | C/T | 2.31567e-05 | 0.00340262 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274222 | CCTCCTTCAACCCTA[C/T]ATGGTCGATCACATC | 158506 |
| rs376055291 | snp | A/G/T | 0.00050343 | 0.0158582 | synonymous-codon, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273564 | CATGGTGTCACTACC[A/G/T]TCTGTGCAACATATG | 158506 |
| rs376089162 | snp | G/T | 0.000189982 | 0.00974449 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273142 | ATAGGTGAAAAGGAT[G/T]ATTTACCAATTCATT | 158506 |
| rs377282086 | snp | C/T | | | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274192 | CTGTCACCTTGTCCA[C/T]CAACGCGGAGTCCAC | 158506 |
| rs377723218 | snp | A/G | 0.000189982 | 0.00974449 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273793 | TGTCAAAGTCAACCA[A/G]CGGTATCGTCCCCTC | 158506 |
| rs527338477 | snp | C/T | | | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273578 | CGTCTGTGCAACATA[C/T]GCTACAAGAGCAACA | 158506 |
| rs537870275 | in-del | -/TTTTTTTTTTTTTTTT | | | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22271985 | TTTTTTTTTTTTTTT[-/TTTTTTTTTTTTTTTT]GAGACAGAGTCTCAC | 158506 |
| rs543921201 | snp | A/G | 0.00105904 | 0.0229869 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22271095 | ACTAAAAATACAAAA[A/G]TTAGCCAGGTGTGGT | 158506 |
| rs546942443 | snp | A/T | | | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273734 | TTCAGAATAACTCAG[A/T]TTCTGGTGCTAAGAA | 158506 |
| rs562071415 | snp | G/T | | | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272606 | TTCTCTTTGAGTACT[G/T]AAGAGCAGCATCAGC | 158506 |
| rs564973817 | snp | A/G | | | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273524 | ACAGGGACCATCTAA[A/G]CTATATTCCACCAGA | 158506 |
| rs568227359 | snp | C/T | | | synonymous-codon, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274185 | GAAACGACTGTCACC[C/T]TGTCCACCAACGCGG | 158506 |
| rs571107659 | snp | G/T | | | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273197 | TTAAAATCTATGGGC[G/T]AATAATTCCGTGCAA | 158506 |
| rs576425301 | snp | C/T | | | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22271010 | ACCACTTTGGAAGGC[C/T]GAGGTGGGTGGATCA | 158506 |
| rs578074070 | snp | C/T | | | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272797 | GCACATGCGTTGTAA[C/T]GCGCACGTGTTACTG | 158506 |
| rs745503528 | snp | C/T | 0.000529661 | 0.016265 | downstream-variant-500B, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274919 | GACAATGTTACTTGT[C/T]AATGCTTTTTTTTTT | 158506 |
| rs745693862 | snp | A/C | 2.28498e-05 | 0.00338 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273650 | TATCTCTAAGTCTGC[A/C]TTTTCCCATCCAGTG | 158506 |
| rs745810939 | snp | C/T | 0.00105904 | 0.0229869 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22271053 | AGTTTGAGACCAGCC[C/T]GGCCAACGTGGTGAA | 158506 |
| rs746291680 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272514 | AAAATAAGTCAGTCC[C/T]AGAAGGCAAAGCTCT | 158506 |
| rs746442308 | snp | A/G | 6.8373e-05 | 0.00584652 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273920 | CTCCTAACTCGGTTC[A/G]TAGCCAAGTGCCAGC | 158506 |
| rs746552589 | snp | C/G | 2.28209e-05 | 0.00337786 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273275 | ATAAAGTATGTCCGC[C/G]CTGTCGTTATCCTGT | 158506 |
| rs746605596 | snp | A/T | 2.28287e-05 | 0.00337844 | stop-gained, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273380 | TGTCTCAGAAAAGCT[A/T]ACAGGCTCATATCAA | 158506 |
| rs746723420 | snp | C/T | | | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22270972 | CAACTTGGCCAGGCG[C/T]GGTGGCTCACGCCTG | 158506 |
| rs746756325 | snp | A/G | 2.27918e-05 | 0.0033757 | synonymous-codon, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273831 | TATACCTCAGAAACA[A/G]CATTATGCGCCACCT | 158506 |
| rs747309382 | snp | C/T | | | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272077 | AACCTCTGCCTCCCA[C/T]GCTCAAGCGATTCTC | 158506 |
| rs747410852 | snp | A/G | 2.28316e-05 | 0.00337865 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274187 | AACGACTGTCACCTT[A/G]TCCACCAACGCGGAG | 158506 |
| rs747722997 | snp | A/G | | | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272206 | GGTCTGGAACTCCTG[A/G]CCTCAAACGATCTGC | 158506 |
| rs747891370 | snp | A/G | 4.58337e-05 | 0.00478694 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273722 | CAGTTGATCATATTC[A/G]GAATAACTCAGATTC | 158506 |
| rs748161130 | snp | C/T | 2.28206e-05 | 0.00337784 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273305 | TGCTGAGAATTGAGG[C/T]GCATAAACGAGGTTC | 158506 |
| rs748592829 | in-del | -/TTTACAA | 6.83675e-05 | 0.00584629 | frameshift-variant, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273989 | TGTAAAGGTGCCACC[-/TTTACAA]TGATATGAATTCTCC | 158506 |
| rs748598374 | snp | C/T | 4.55783e-05 | 0.00477358 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274130 | TGAGCCCTCAGTTTA[C/T]ACAAACAGATGCAAT | 158506 |
| rs748694283 | in-del | -/C | 2.28269e-05 | 0.0033783 | frameshift-variant, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273413 | GCCGCCATAAGAGAG[-/C]TCGAAAACAAGTTAC | 158506 |
| rs748844779 | snp | C/G | 0.0026455 | 0.0362733 | downstream-variant-500B, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274705 | TTCACATTTTAGGAA[C/G]TGAAATTTTAAGGTA | 158506 |
| rs749058196 | snp | C/T | 2.28271e-05 | 0.00337832 | synonymous-codon, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273432 | AAAACAAGTTACCAG[C/T]GCTTCGCTTGAAAAA | 158506 |
| rs749258396 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272446 | CACAGACATATCATC[C/T]TATCTTATTCCAATG | 158506 |
| rs749454003 | snp | C/G | 2.27889e-05 | 0.00337549 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274001 | CACCTGATATGAATT[C/G]TCCTCCACTACGTGC | 158506 |
| rs750094780 | in-del | -/CTG | 2.28258e-05 | 0.00337822 | cds-indel, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273370 | GAACATACTTGTCTC[-/CTG]AGAAAAGCTTACAGG | 158506 |
| rs750226040 | snp | C/T | 2.29316e-05 | 0.00338604 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273182 | AATGTGATTTGCCTA[C/T]TAAAATCTATGGGCG | 158506 |
| rs750306802 | snp | A/G | 9.11858e-05 | 0.00675163 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273819 | CCCTCATCATATTAT[A/G]CCTCAGAAACAGCAT | 158506 |
| rs750466096 | snp | A/G | 2.29339e-05 | 0.00338621 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273181 | AAATGTGATTTGCCT[A/G]TTAAAATCTATGGGC | 158506 |
| rs750553380 | snp | A/G | 2.39109e-05 | 0.00345758 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274262 | AGAGAAGACATAGAC[A/G]GTATTAAGGATGATA | 158506 |
| rs750793510 | snp | C/T | 2.28235e-05 | 0.00337805 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273367 | AAGAGAACATACTTG[C/T]CTCAGAAAAGCTTAC | 158506 |
| rs750897233 | snp | A/G/T | 9.12562e-05 | 0.00675433 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273458 | AAAAAGTTCGTCCTC[A/G/T]TATTGCTCCGCCACA | 158506 |
| rs751390940 | snp | A/G | 2.27899e-05 | 0.00337557 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274108 | TTCACCGAAAATCAA[A/G]AAACCTTGAGCCCTC | 158506 |
| rs751393169 | snp | A/G | | | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22271474 | TATGCCCACCAATCT[A/G]CAGCTATTACGTCAC | 158506 |
| rs751398593 | snp | G/T | 2.27907e-05 | 0.00337562 | synonymous-codon, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273990 | TGTAAAGGTGCCACC[G/T]GATATGAATTCTCCT | 158506 |
| rs751402380 | in-del | -/AA | 2.28219e-05 | 0.00337794 | frameshift-variant, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273357 | TCAGCAGTGCAAGAG[-/AA]CATACTTGTCTCAGA | 158506 |
| rs751467489 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272297 | CACTGCCTTTTACAT[A/G]ATTTTTCCTTGACGA | 158506 |
| rs751650282 | snp | C/G | 5.0005e-05 | 0.005 | utr-variant-3-prime, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274299 | TTTGGAACTGAAGAC[C/G]TGATGGGAAAAAAAC | 158506 |
| rs751685596 | snp | A/G | 2.41894e-05 | 0.00347766 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273037 | TGTGAATATAACAAA[A/G]AAGGGAAGTACTACT | 158506 |
| rs752008612 | snp | C/T | 6.8657e-05 | 0.00585865 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273604 | CAACATAATCAGCCA[C/T]ATAAGGATATCCAGG | 158506 |
| rs752284658 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22271353 | TAGCTACTTGCTCCA[A/G]GAAATACTTTTTCCT | 158506 |
| rs752334835 | snp | A/C | 2.28517e-05 | 0.00338013 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273629 | TCCAGGCTCCTCCCC[A/C]AGAACTATCTCTAAG | 158506 |
| rs752525647 | snp | C/G | 0.000159517 | 0.00892933 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274142 | TTACACAAACAGATG[C/G]AATGGATCATAGAAG | 158506 |
| rs752563118 | in-del | -/TT | | | downstream-variant-500B, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274925 | GTTACTTGTTAATGC[-/TT]TTTTTTTTTTTTTTA | 158506 |
| rs752756344 | snp | A/T | 2.36939e-05 | 0.00344186 | synonymous-codon, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273063 | CTACTCTAAAGGAGT[A/T]AAACTGGTGAGAAAA | 158506 |
| rs752813595 | snp | A/G | 2.28579e-05 | 0.0033806 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273215 | TAATTCCGTGCAAGC[A/G]TGCTTTTTGCTATCA | 158506 |
| rs752936958 | snp | A/C | | | downstream-variant-500B, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274710 | ATTTTAGGAACTGAA[A/C]TTTTAAGGTACAATA | 158506 |
| rs752998178 | snp | C/T | 2.28457e-05 | 0.00337969 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273790 | GAGTGTCAAAGTCAA[C/T]CAGCGGTATCGTCCC | 158506 |
| rs753049993 | snp | A/G | 0.000529661 | 0.016265 | downstream-variant-500B, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274674 | TAAAGCAGACAGCTA[A/G]ATGGTAGATAATTAT | 158506 |
| rs753797712 | in-del | -/CT | 2.28212e-05 | 0.00337788 | frameshift-variant, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273345 | TGTAGTATTGTTCAG[-/CT]CAGTGCAAGAGAACA | 158506 |
| rs753912921 | snp | A/G/T | 6.84663e-05 | 0.00585058 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273362 | AGTGCAAGAGAACAT[A/G/T]CTTGTCTCAGAAAAG | 158506 |
| rs753973538 | snp | A/C | 0.000529661 | 0.016265 | utr-variant-5-prime, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272924 | CTTCACGTTAGCAGA[A/C]GAATTCCTTTAAACG | 158506 |
| rs754135127 | snp | C/G | | | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272806 | TTGTAATGCGCACGT[C/G]TTACTGGCACATGAC | 158506 |
| rs754283975 | snp | C/T | 2.2842e-05 | 0.00337942 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273229 | CATGCTTTTTGCTAT[C/T]ACTGTGCTAATTTAT | 158506 |
| rs754670109 | snp | A/G | 4.566e-05 | 0.00477786 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273383 | CTCAGAAAAGCTTAC[A/G]GGCTCATATCAAACG | 158506 |
| rs754675728 | snp | A/G | 2.27894e-05 | 0.00337553 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273991 | GTAAAGGTGCCACCT[A/G]ATATGAATTCTCCTC | 158506 |
| rs754913947 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272830 | ACATGACTCCCGGTC[C/T]CTTGTGAGCCGAAAC | 158506 |
| rs755088322 | snp | C/T | 2.40298e-05 | 0.00346617 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273046 | AACAAAGAAGGGAAG[C/T]ACTACTCTAAAGGAG | 158506 |
| rs755376051 | snp | C/T | 2.27897e-05 | 0.00337555 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274085 | ATAACCTTAACATTT[C/T]ACCTCAGTTCACCGA | 158506 |
| rs755489968 | snp | A/G | 3.31098e-05 | 0.00406864 | utr-variant-3-prime, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274301 | TGGAACTGAAGACCT[A/G]ATGGGAAAAAAACCT | 158506 |
| rs755601858 | snp | G/T | 2.28277e-05 | 0.00337836 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273514 | AGACTGCAAGACAGG[G/T]ACCATCTAAGCTATA | 158506 |
| rs755758465 | in-del | -/AA | 2.28258e-05 | 0.00337822 | frameshift-variant, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273373 | ACATACTTGTCTCAG[-/AA]AAGCTTACAGGCTCA | 158506 |
| rs755802073 | snp | A/G | | | downstream-variant-500B, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274729 | TAAGGTACAATAAGT[A/G]TATAGTGCATTTCGT | 158506 |
| rs756255824 | in-del | -/TG | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272403 | AAGGTATGTGTATTT[-/TG]TGTGTATGTATATAT | 158506 |
| rs756658706 | snp | A/C | 2.36167e-05 | 0.00343624 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273066 | CTCTAAAGGAGTTAA[A/C]CTGGTGAGAAAAAAG | 158506 |
| rs757089763 | in-del | -/G | 2.28214e-05 | 0.0033779 | frameshift-variant, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273359 | GCAGTGCAAGAGAAC[-/G]ATACTTGTCTCAGAA | 158506 |
| rs757094031 | snp | A/G | 0.00105904 | 0.0229869 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22271031 | GGGTGGATCACCTGA[A/G]GTCAGGAGTTTGAGA | 158506 |
| rs757236420 | snp | C/G | 4.56971e-05 | 0.00477979 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273640 | CCCCCAGAACTATCT[C/G]TAAGTCTGCCTTTTC | 158506 |
| rs757323546 | snp | A/G | | | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22271753 | AATGTCTGCACATTC[A/G]GGAGAATAGAGGTGC | 158506 |
| rs757547937 | snp | A/C/G | 4.5576e-05 | 0.0047735 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274013 | ATTCTCCTCCACTAC[A/C/G]TGCTCCCCAGTCTCA | 158506 |
| rs757600955 | snp | A/G | 2.27905e-05 | 0.00337561 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274151 | CAGATGCAATGGATC[A/G]TAGAAGGTGGCCTGC | 158506 |
| rs757647131 | snp | A/G | 2.28219e-05 | 0.00337794 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273247 | TGTGCTAATTTATAT[A/G]ACAAAGTCGGATATA | 158506 |
| rs758361684 | snp | C/T | 0.000114008 | 0.00754924 | stop-gained, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274174 | TGGCCTGCATGGAAA[C/T]GACTGTCACCTTGTC | 158506 |
| rs758391803 | snp | C/T | 6.83652e-05 | 0.00584619 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273986 | TTATTGTAAAGGTGC[C/T]ACCTGATATGAATTC | 158506 |
| rs758753678 | snp | A/C | 2.28243e-05 | 0.00337811 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273371 | GAACATACTTGTCTC[A/C]GAAAAGCTTACAGGC | 158506 |
| rs758820714 | snp | A/G | | | synonymous-codon, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273984 | TATTATTGTAAAGGT[A/G]CCACCTGATATGAAT | 158506 |
| rs759371826 | multinucleotide-polymorphism | AAAAACCCCAA/GTCAACAACCC | | | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22271174 | AAAAAAAAAAAAAGA[AAAAACCCCAA/GTCAACAACCC]AACAAGCCAGAGCCA | 158506 |
| rs759449365 | snp | C/T | 2.32072e-05 | 0.00340633 | stop-gained, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274228 | TCAACCCTACATGGT[C/T]GATCACATCATTCAC | 158506 |
| rs759730992 | snp | C/T | 2.28906e-05 | 0.00338302 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273206 | ATGGGCGAATAATTC[C/T]GTGCAAGCATGCTTT | 158506 |
| rs759992232 | snp | C/T | 4.58111e-05 | 0.00478576 | synonymous-codon, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273762 | GAAGCCAACACCTCC[C/T]GACTATTATCCTGAG | 158506 |
| rs760102116 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22271264 | ACATAATTCTCTGTC[A/G]CTGTGTAAAACAATA | 158506 |
| rs760244026 | snp | A/T | 2.30065e-05 | 0.00339157 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273113 | ACCGTTGGGGGGACA[A/T]TAAGATAAACATCAT | 158506 |
| rs760540672 | snp | A/T | 0.00581083 | 0.0535878 | downstream-variant-500B, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274480 | TTGTGGTTTTTATTT[A/T]TTTATTTTTTGGTGA | 158506 |
| rs760755951 | snp | C/G | 2.28201e-05 | 0.0033778 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273348 | TAGTATTGTTCAGCA[C/G]TGCAAGAGAACATAC | 158506 |
| rs760765051 | snp | A/C | 2.46621e-05 | 0.00351147 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273004 | AATATGAACAAGATG[A/C]CTGCTGGTGAACAAG | 158506 |
| rs760806744 | in-del | -/G | 2.30657e-05 | 0.00339592 | frameshift-variant, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273104 | TTCCTGGTTACCGTT[-/G]GGGGGACATTAAGAT | 158506 |
| rs760919712 | snp | A/C | 2.27899e-05 | 0.00337557 | synonymous-codon, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273939 | CCAAGTGCCAGCTCT[A/C]ACCACGACCTACGAT | 158506 |
| rs761670940 | snp | C/T | 2.43463e-05 | 0.00348892 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273028 | GAACAAGAATGTGAA[C/T]ATAACAAAGAAGGGA | 158506 |
| rs761726092 | snp | A/G | 2.295e-05 | 0.0033874 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273163 | CCAATTCATTTCTGT[A/G]ACAAATGTGATTTGC | 158506 |
| rs761825857 | snp | G/T | 6.86499e-05 | 0.00585835 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273565 | ATGGTGTCACTACCG[G/T]CTGTGCAACATATGC | 158506 |
| rs761921600 | snp | G/T | 2.28185e-05 | 0.00337768 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273448 | GCTTCGCTTGAAAAA[G/T]TTCGTCCTCATATTG | 158506 |
| rs761921896 | snp | A/T | | | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272807 | TGTAATGCGCACGTG[A/T]TACTGGCACATGACT | 158506 |
| rs762040737 | in-del | -/AAG | 2.42527e-05 | 0.00348221 | cds-indel, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273035 | AATGTGAATATAACA[-/AAG]AAGGGAAGTACTACT | 158506 |
| rs762326894 | snp | A/C | 2.27907e-05 | 0.00337562 | synonymous-codon, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274098 | TTTACCTCAGTTCAC[A/C]GAAAATCAAGAAACC | 158506 |
| rs762502325 | snp | C/G | 2.28519e-05 | 0.00338015 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273535 | CTAAGCTATATTCCA[C/G]CAGAACAGCACACCA | 158506 |
| rs762534152 | snp | C/T | 9.17431e-05 | 0.00677223 | synonymous-codon, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274203 | TCCACCAACGCGGAG[C/T]CCACCTCCTTCAACC | 158506 |
| rs762773446 | snp | C/T | 2.28227e-05 | 0.00337799 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273329 | GAGGTTCTGTCTTCA[C/T]GTGTAGTATTGTTCA | 158506 |
| rs762775977 | snp | C/T | | | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22271263 | AACATAATTCTCTGT[C/T]GCTGTGTAAAACAAT | 158506 |
| rs762964144 | in-del | -/CCTCT | 2.28206e-05 | 0.00337784 | frameshift-variant, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273353 | TGTTCAGCAGTGCAA[-/CCTCT]GAGAACATACTTGTC | 158506 |
| rs762971677 | snp | C/T | | | utr-variant-3-prime, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274422 | AAAGGTGACCTCTGA[C/T]GATTTCCTGAAATAA | 158506 |
| rs763012875 | snp | A/C | | | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272571 | CACGCCCATCAGTTT[A/C]TGTTTCCATGAAGAC | 158506 |
| rs763092276 | snp | C/T | 2.29211e-05 | 0.00338526 | synonymous-codon, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273735 | TCAGAATAACTCAGA[C/T]TCTGGTGCTAAGAAG | 158506 |
| rs763359039 | snp | A/C | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22271178 | AAAAAAAAAGAGTCA[A/C]CAACCCAACAAGCCA | 158506 |
| rs763570109 | snp | A/C | 4.57959e-05 | 0.00478496 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273571 | TCACTACCGTCTGTG[A/C]AACATATGCTACAAG | 158506 |
| rs763632908 | snp | A/G | 4.56579e-05 | 0.00477775 | synonymous-codon, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273795 | TCAAAGTCAACCAGC[A/G]GTATCGTCCCCTCAT | 158506 |
| rs763689769 | in-del | -/T | 0.497269 | 0.0368526 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22271960 | ATCTATTCACTCCTG[-/T]TTTTTTTTTTTTTTT | 158506 |
| rs763838901 | snp | C/T | 4.5582e-05 | 0.00477377 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273944 | TGCCAGCTCTAACCA[C/T]GACCTACGATCCATC | 158506 |
| rs763886114 | snp | C/T | 0.00105904 | 0.0229869 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22271449 | ACTTGCTTCAATATT[C/T]TCCTCCTGCTATGCC | 158506 |
| rs763889082 | in-del | -/CCTCCCACGCTCA | 2.28204e-05 | 0.00337782 | frameshift-variant, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273354 | GTTCAGCAGTGCAAG[-/CCTCCCACGCTCA]AGAACATACTTGTCT | 158506 |
| rs764022720 | snp | A/T | 0.00105904 | 0.0229869 | downstream-variant-500B, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274481 | TGTGGTTTTTATTTT[A/T]TTATTTTTTGGTGAT | 158506 |
| rs764119069 | snp | C/G | 2.45008e-05 | 0.00349997 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273016 | ATGCCTGCTGGTGAA[C/G]AAGAATGTGAATATA | 158506 |
| rs764350145 | snp | C/T | | | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22271516 | AATCCCAATTAGAGG[C/T]CTGCCTTGCAAGACC | 158506 |
| rs764446277 | snp | G/T | | | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272773 | GCCTCCTAGGCTGGG[G/T]AAGATGGTGCACATG | 158506 |
| rs764732822 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272109 | TGCCTCCTGAGTAGC[C/T]GAGATTACAGGCGCG | 158506 |
| rs764968618 | snp | A/T | 0.00211696 | 0.0324653 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272742 | GAGGGTTGGGGAGGC[A/T]TCGGATCGCACTTTC | 158506 |
| rs765117844 | snp | C/T | | | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22271051 | GGAGTTTGAGACCAG[C/T]CCGGCCAACGTGGTG | 158506 |
| rs765213974 | snp | C/T | 0.000114187 | 0.00755515 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273794 | GTCAAAGTCAACCAG[C/T]GGTATCGTCCCCTCA | 158506 |
| rs765311738 | snp | C/T | | | utr-variant-3-prime, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274345 | TGTACTGTGGATAAG[C/T]GGCTCAGTTCAGCAG | 158506 |
| rs765581221 | snp | C/T | 4.77629e-05 | 0.00488663 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274261 | CAGAGAAGACATAGA[C/T]GGTATTAAGGATGAT | 158506 |
| rs765752654 | snp | C/T | 2.2824e-05 | 0.00337809 | synonymous-codon, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273363 | GTGCAAGAGAACATA[C/T]TTGTCTCAGAAAAGC | 158506 |
| rs766160644 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272784 | TGGGGAAGATGGTGC[A/G]CATGCGTTGTAATGC | 158506 |
| rs766192463 | snp | A/C | 6.83691e-05 | 0.00584635 | synonymous-codon, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273987 | TATTGTAAAGGTGCC[A/C]CCTGATATGAATTCT | 158506 |
| rs766447242 | in-del | -/TGTGACGCGATC | 2.28209e-05 | 0.00337786 | cds-indel, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273341 | CATGTGTAGTATTGT[-/TGTGACGCGATC]TCAGCAGTGCAAGAG | 158506 |
| rs766657224 | snp | A/G | 2.43404e-05 | 0.00348849 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273029 | AACAAGAATGTGAAT[A/G]TAACAAAGAAGGGAA | 158506 |
| rs766735191 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22271234 | CTGCTATGTGGTAAC[C/T]GAGTACTGAAACCAA | 158506 |
| rs766761938 | snp | G/T | 0.00105904 | 0.0229869 | downstream-variant-500B, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274492 | TTTTTTTATTTTTTG[G/T]TGATATGTTAACCTG | 158506 |
| rs766786548 | snp | C/T | 2.28131e-05 | 0.00337728 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273467 | GTCCTCATATTGCTC[C/T]GCCACAAACTGAAAT | 158506 |
| rs767292006 | in-del | -/TTT | 0.00581083 | 0.0535878 | downstream-variant-500B, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274476 | GTATTGTGGTTTTTA[-/TTT]TTTTTTTATTTTTTG | 158506 |
| rs767300620 | snp | C/T | 2.28584e-05 | 0.00338064 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273626 | ATATCCAGGCTCCTC[C/T]CCCAGAACTATCTCT | 158506 |
| rs767538011 | snp | A/G | 2.32177e-05 | 0.0034071 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274229 | CAACCCTACATGGTC[A/G]ATCACATCATTCACA | 158506 |
| rs767663667 | snp | A/T | 0.000159743 | 0.00893565 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273334 | TCTGTCTTCATGTGT[A/T]GTATTGTTCAGCAGT | 158506 |
| rs767753116 | snp | A/G | 0.000114409 | 0.00756249 | synonymous-codon, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273207 | TGGGCGAATAATTCC[A/G]TGCAAGCATGCTTTT | 158506 |
| rs767926689 | snp | C/T | 2.28632e-05 | 0.00338098 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273778 | GACTATTATCCTGAG[C/T]GTCAAAGTCAACCAG | 158506 |
| rs768235388 | snp | A/G | 2.28188e-05 | 0.0033777 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273281 | TATGTCCGCGCTGTC[A/G]TTATCCTGTGCTGAG | 158506 |
| rs768294244 | snp | A/G | | | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22270983 | GGCGCGGTGGCTCAC[A/G]CCTGTAATCTCACCA | 158506 |
| rs768679998 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22271074 | ACGTGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 158506 |
| rs768758159 | snp | C/T | 2.2984e-05 | 0.00338991 | synonymous-codon, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273126 | CATTAAGATAAACAT[C/T]ATAGGTGAAAAGGAT | 158506 |
| rs768845651 | snp | C/G | 2.27899e-05 | 0.00337557 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274075 | TCTCACCATTATAAC[C/G]TTAACATTTTACCTC | 158506 |
| rs769233354 | in-del | -/C | 0.000182838 | 0.00955959 | frameshift-variant, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273625 | GATATCCAGGCTCCT[-/C]CCCCAGAACTATCTC | 158506 |
| rs769320288 | snp | A/G/T | 4.56499e-05 | 0.00477737 | synonymous-codon, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273438 | AGTTACCAGCGCTTC[A/G/T]CTTGAAAAAGTTCGT | 158506 |
| rs769394893 | snp | C/T | | | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272359 | AGGTGATTTTAAACT[C/T]ACTGTATCGTGAAAT | 158506 |
| rs769753747 | snp | A/G | 2.28201e-05 | 0.0033778 | synonymous-codon, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273306 | GCTGAGAATTGAGGC[A/G]CATAAACGAGGTTCT | 158506 |
| rs769844460 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22271780 | GTGCCACAATTATGG[A/G]TGGAGTGGAGGCAGA | 158506 |
| rs769857695 | snp | G/T | 2.28825e-05 | 0.00338242 | synonymous-codon, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273567 | GGTGTCACTACCGTC[G/T]GTGCAACATATGCTA | 158506 |
| rs770396547 | snp | A/C | 0.000529661 | 0.016265 | downstream-variant-500B, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274726 | TTTTAAGGTACAATA[A/C]GTGTATAGTGCATTT | 158506 |
| rs770606914 | snp | C/G | 4.97828e-05 | 0.00498888 | utr-variant-5-prime, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272941 | AATTCCTTTAAACGT[C/G]ATTTTTGAGGAAGTA | 158506 |
| rs770848347 | snp | C/T | 2.28652e-05 | 0.00338114 | synonymous-codon, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273549 | ACCAGAACAGCACAC[C/T]ATGGTGTCACTACCG | 158506 |
| rs770999882 | snp | G/T | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22271859 | AAGGTAAGATGTGAG[G/T]AAATGTGGGCTAAAT | 158506 |
| rs771214795 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272481 | ATTTAAGGTAGTTCA[C/T]AAAAATGCAATAGGA | 158506 |
| rs771428921 | snp | A/T | 2.48444e-05 | 0.00352443 | utr-variant-5-prime, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272973 | ACAAACCTAAATATG[A/T]GTCTGAACTCCAAGG | 158506 |
| rs771752633 | snp | G/T | 4.60554e-05 | 0.0047985 | synonymous-codon, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273108 | TGGTTACCGTTGGGG[G/T]GACATTAAGATAAAC | 158506 |
| rs771809021 | snp | A/C | 4.57556e-05 | 0.00478286 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273686 | CCGTTAGTATTTTTA[A/C]GAGAAAACATGGCAA | 158506 |
| rs772045465 | snp | C/T | | | utr-variant-3-prime, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274318 | TGGGAAAAAAACCTT[C/T]AAGTTCTATACTGTA | 158506 |
| rs772289644 | snp | C/G | 0.00158814 | 0.0281345 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272534 | GGCAAAGCTCTGCAG[C/G]GCCTGCTGGGAATTT | 158506 |
| rs772317567 | in-del | -/ATTT | 4.76701e-05 | 0.00488188 | frameshift-variant, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273056 | GAAGTACTACTCTAA[-/ATTT]AGGAGTTAAACTGGT | 158506 |
| rs772415570 | in-del | -/A | 2.54391e-05 | 0.00356636 | utr-variant-3-prime, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274307 | TGAAGACCTGATGGG[-/A]AAAAAACCTTCAAGT | 158506 |
| rs772655512 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22271915 | CAAGAACAGCAAATG[C/T]CTAAAAAATGTCTAG | 158506 |
| rs772676043 | snp | A/G | 2.27897e-05 | 0.00337555 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274051 | AATCCATCTGCAAGT[A/G]AATTTGCTTCTCACC | 158506 |
| rs772746024 | snp | A/C | 2.27894e-05 | 0.00337553 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274097 | TTTTACCTCAGTTCA[A/C]CGAAAATCAAGAAAC | 158506 |
| rs772801021 | snp | A/G | 4.57818e-05 | 0.00478422 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274199 | CTTGTCCACCAACGC[A/G]GAGTCCACCTCCTTC | 158506 |
| rs772925814 | snp | C/G | 6.84603e-05 | 0.00585025 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273313 | ATTGAGGCGCATAAA[C/G]GAGGTTCTGTCTTCA | 158506 |
| rs773161307 | snp | C/T | 2.28258e-05 | 0.00337822 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273428 | CTCGAAAACAAGTTA[C/T]CAGCGCTTCGCTTGA | 158506 |
| rs773241043 | snp | A/G | | | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22271061 | ACCAGCCCGGCCAAC[A/G]TGGTGAAACCCCGTC | 158506 |
| rs773356354 | snp | A/G | | | utr-variant-3-prime, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274392 | CTTTGTTCCTCTGGT[A/G]TGGTAAATTGACCTA | 158506 |
| rs773388595 | snp | A/T | 2.29184e-05 | 0.00338507 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273726 | TGATCATATTCAGAA[A/T]AACTCAGATTCTGGT | 158506 |
| rs773397514 | in-del | -/GTT | 4.74845e-05 | 0.00487237 | cds-indel, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273060 | TACTACTCTAAAGGA[-/GTT]GTTAAACTGGTGAGA | 158506 |
| rs773493451 | in-del | -/A | 2.54391e-05 | 0.00356636 | utr-variant-3-prime, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274306 | TGAAGACCTGATGGG[-/A]AAAAAAACCTTCAAG | 158506 |
| rs773599014 | snp | A/G | 0.000251754 | 0.0112167 | synonymous-codon, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273570 | GTCACTACCGTCTGT[A/G]CAACATATGCTACAA | 158506 |
| rs773832025 | snp | A/G | 2.48531e-05 | 0.00352504 | utr-variant-5-prime, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272968 | AGTAGACAAACCTAA[A/G]TATGTGTCTGAACTC | 158506 |
| rs773907840 | snp | A/G | 2.31532e-05 | 0.00340236 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274223 | CTCCTTCAACCCTAC[A/G]TGGTCGATCACATCA | 158506 |
| rs774297449 | snp | C/T | | | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272757 | ATCGGATCGCACTTT[C/T]GCCTCCTAGGCTGGG | 158506 |
| rs774922174 | snp | A/T | 2.30158e-05 | 0.00339225 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273110 | GTTACCGTTGGGGGG[A/T]CATTAAGATAAACAT | 158506 |
| rs775002767 | snp | C/G | 2.27923e-05 | 0.00337574 | synonymous-codon, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273915 | AGTTACTCCTAACTC[C/G]GTTCGTAGCCAAGTG | 158506 |
| rs775136948 | snp | A/G | 2.59464e-05 | 0.00360174 | utr-variant-3-prime, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274320 | GGAAAAAAACCTTCA[A/G]GTTCTATACTGTACT | 158506 |
| rs775151071 | snp | A/G | 0.000529661 | 0.016265 | downstream-variant-500B, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274958 | AGAATCGTTCAAATC[A/G]CATAATGTACCACAC | 158506 |
| rs775551772 | in-del | -/A | 0.0026455 | 0.0362733 | downstream-variant-500B, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274479 | TTGTGGTTTTTATTT[-/A]TTTTATTTTTTGGTG | 158506 |
| rs775692278 | snp | C/T | 0.000114112 | 0.00755269 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273437 | AAGTTACCAGCGCTT[C/T]GCTTGAAAAAGTTCG | 158506 |
| rs775822302 | snp | C/T | 4.55789e-05 | 0.00477361 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274066 | GAATTTGCTTCTCAC[C/T]ATTATAACCTTAACA | 158506 |
| rs776123817 | snp | C/G | | | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22271027 | AGGTGGGTGGATCAC[C/G]TGAAGTCAGGAGTTT | 158506 |
| rs776203489 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272558 | GGAATTTATTCCCCA[C/T]GCCCATCAGTTTCTG | 158506 |
| rs776218615 | snp | A/G | 9.11702e-05 | 0.00675106 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273952 | CTAACCACGACCTAC[A/G]ATCCATCATCTGGAT | 158506 |
| rs776273915 | snp | C/T | 2.27892e-05 | 0.00337551 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274082 | ATTATAACCTTAACA[C/T]TTTACCTCAGTTCAC | 158506 |
| rs776287450 | snp | G/T | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272678 | CTCACTAGAGTGGTG[G/T]GACAGGGTAGGTGAG | 158506 |
| rs776725243 | snp | C/T | 2.28178e-05 | 0.00337763 | synonymous-codon, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273292 | TGTCGTTATCCTGTG[C/T]TGAGAATTGAGGCGC | 158506 |
| rs776742281 | snp | C/T | 2.28225e-05 | 0.00337797 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273440 | TTACCAGCGCTTCGC[C/T]TGAAAAAGTTCGTCC | 158506 |
| rs777407122 | snp | C/G/T | 4.56947e-05 | 0.00477971 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273637 | CCTCCCCCAGAACTA[C/G/T]CTCTAAGTCTGCCTT | 158506 |
| rs777814165 | snp | A/C | 2.27889e-05 | 0.00337549 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273844 | CAGCATTATGCGCCA[A/C]CTCCATCTCCATCAT | 158506 |
| rs778065251 | snp | G/T | 0.000455679 | 0.0150875 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273995 | AGGTGCCACCTGATA[G/T]GAATTCTCCTCCACT | 158506 |
| rs778221443 | snp | C/T | 1.6473e-05 | 0.00286988 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273068 | CTAAAGGAGTTAAAC[C/T]GGTGAGAAAAAAGAA | 158506 |
| rs778274339 | snp | C/T | 2.28517e-05 | 0.00338013 | synonymous-codon, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273225 | CAAGCATGCTTTTTG[C/T]TATCACTGTGCTAAT | 158506 |
| rs778419374 | snp | A/G | | | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272022 | GAGTCTCACTCTGTC[A/G]CCCAGGCTGGAGTGC | 158506 |
| rs778740406 | snp | A/G | 6.86091e-05 | 0.00585661 | | | GRCh38.p7 | X:22273555 | ACAGCACACCATGGT[A/G]TCACTACCGTCTGTG | 158506 |
| rs778791731 | snp | C/T | 2.28454e-05 | 0.00337967 | synonymous-codon, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273645 | AGAACTATCTCTAAG[C/T]CTGCCTTTTCCCATC | 158506 |
| rs779213768 | snp | C/T | 4.56387e-05 | 0.00477674 | synonymous-codon, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273270 | CGGATATAAAGTATG[C/T]CCGCGCTGTCGTTAT | 158506 |
| rs779254699 | in-del | -/TCA | 0.000410565 | 0.0143218 | cds-indel, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273807 | AGCGGTATCGTCCCC[-/TCA]TCATATTATACCTCA | 158506 |
| rs779722903 | in-del | -/TGAGA | 2.28295e-05 | 0.00337849 | frameshift-variant, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273378 | TTGTCTCAGAAAAGC[-/TGAGA]TTACAGGCTCATATC | 158506 |
| rs779729437 | snp | C/T | 9.12773e-05 | 0.00675502 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273274 | TATAAAGTATGTCCG[C/T]GCTGTCGTTATCCTG | 158506 |
| rs779817965 | snp | C/G | 0.00158814 | 0.0281345 | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22271718 | AGTAGGGGTTGACAG[C/G]CAACGAAGCTAAAAG | 158506 |
| rs779878074 | snp | A/T | 2.28261e-05 | 0.00337824 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273375 | ATACTTGTCTCAGAA[A/T]AGCTTACAGGCTCAT | 158506 |
| rs779968707 | snp | A/C | 2.27918e-05 | 0.0033757 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273830 | TTATACCTCAGAAAC[A/C]GCATTATGCGCCACC | 158506 |
| rs780385554 | snp | A/G | 6.83636e-05 | 0.00584612 | synonymous-codon, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273855 | GCCACCTCCATCTCC[A/G]TCATCACCAGTAAAC | 158506 |
| rs780464768 | snp | C/T | | | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272055 | TGACGCGATCTCAGC[C/T]CACTGCAACCTCTGC | 158506 |
| rs780482798 | snp | A/G | 2.28909e-05 | 0.00338303 | synonymous-codon, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273588 | ACATATGCTACAAGA[A/G]CAACATAATCAGCCA | 158506 |
| rs780625523 | snp | C/T | 2.2817e-05 | 0.00337757 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274186 | AAACGACTGTCACCT[C/T]GTCCACCAACGCGGA | 158506 |
| rs780775265 | snp | A/G | | | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272112 | CTCCTGAGTAGCTGA[A/G]ATTACAGGCGCGTGC | 158506 |
| rs780904588 | snp | C/T | 2.28342e-05 | 0.00337884 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273397 | CAGGCTCATATCAAA[C/T]GCCGCCATAAGAGAG | 158506 |
| rs780957784 | snp | A/G | 2.28092e-05 | 0.00337699 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273475 | ATTGCTCCGCCACAA[A/G]CTGAAATCTCTGACA | 158506 |
| rs781041623 | in-del | -/CC | 2.2823e-05 | 0.00337801 | frameshift-variant, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22273364 | GCAAGAGAACATACT[-/CC]TGTCTCAGAAAAGCT | 158506 |
| rs781065711 | snp | C/T | 0.000529661 | 0.016265 | utr-variant-5-prime, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272917 | GGGTGGCCTTCACGT[C/T]AGCAGAAGAATTCCT | 158506 |
| rs781398534 | snp | A/G | 0.000529661 | 0.016265 | downstream-variant-500B, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274590 | TGCTGTTTCTTAAAC[A/G]TATTTTACCACTGAT | 158506 |
| rs781596683 | snp | C/G | 4.57498e-05 | 0.00478255 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274196 | CACCTTGTCCACCAA[C/G]GCGGAGTCCACCTCC | 158506 |
| rs781643764 | snp | A/G | 2.54327e-05 | 0.00356591 | utr-variant-3-prime, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274308 | GAAGACCTGATGGGA[A/G]AAAAACCTTCAAGTT | 158506 |
| rs781743143 | snp | C/T | 2.27902e-05 | 0.00337559 | missense, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274112 | CCGAAAATCAAGAAA[C/T]CTTGAGCCCTCAGTT | 158506 |
| rs796446815 | in-del | -/AG | | | upstream-variant-2KB, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22272008 | TTTTTTTTGAGACAG[-/AG]TCTCACTCTGTCGCC | 158506 |
| rs796842442 | in-del | -/T | | | downstream-variant-500B, intron-variant | ZNF645, PTCHD1-AS | GRCh38.p7 | X:22274940 | TTTTTTTTTTTTTTT[-/T]ACAGAATCGTTCAAA | 158506 |