| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs27139 | snp | G/T | 0.487871 | 0.076925 | intron-variant | PPWD1 | GRCh38.p7 | 5:65585354 | AGATAATGAATAAAG[G/T]GTCATGCTGAGATTA | 23398 |
| rs27140 | snp | A/G | 0.487809 | 0.0771174 | intron-variant | PPWD1 | GRCh38.p7 | 5:65585751 | TAACTGGCTTTATTT[A/G]GGTTATTGAGAAAGA | 23398 |
| rs27141 | snp | A/G | 0.470103 | 0.118552 | synonymous-codon | PPWD1 | GRCh38.p7 | 5:65586109 | ACGACATGACAGGCC[A/G]TACACACTCAGCATG | 23398 |
| rs27142 | snp | A/C | 0.487746 | 0.0773096 | downstream-variant-500B | PPWD1 | GRCh38.p7 | 5:65588028 | TTTAATTTTGAATAC[A/C]TGCCAGATATTCCGC | 23398 |
| rs36223 | snp | C/T | 0 | 0 | intron-variant | PPWD1 | GRCh38.p7 | 5:65570148 | GAAAATTAGATACAG[C/T]GAAGCCTTATAATGT | 23398 |
| rs36224 | snp | A/G | 0.487809 | 0.0771174 | intron-variant | PPWD1 | GRCh38.p7 | 5:65570767 | AGGGAAGAAGGAAAG[A/G]GAGATCTTTTTTTCT | 23398 |
| rs36225 | snp | C/T | 0.47934 | 0.0995154 | intron-variant | PPWD1 | GRCh38.p7 | 5:65571099 | TTCACAGATATTGAA[C/T]GTTTGCCCTTTGAGA | 23398 |
| rs37333 | snp | G/T | 0.377582 | 0.214995 | intron-variant | PPWD1 | GRCh38.p7 | 5:65578561 | gtatcttgttttagt[G/T]tggatttccctggca | 23398 |
| rs37334 | snp | G/T | 0.374 | 0.217081 | intron-variant | PPWD1 | GRCh38.p7 | 5:65579278 | AATTGATACCTTTTG[G/T]GGGGTAGAGAAACAC | 23398 |
| rs37335 | snp | A/G | 0.377385 | 0.215112 | intron-variant | PPWD1 | GRCh38.p7 | 5:65580562 | tctgttgcccaggct[A/G]gagtgcagtgacgtg | 23398 |
| rs37336 | snp | A/G | 0.377385 | 0.215112 | intron-variant | PPWD1 | GRCh38.p7 | 5:65580663 | ggattataggtgcat[A/G]ccaccatacccagct | 23398 |
| rs37337 | snp | C/T | 0.487809 | 0.0771174 | intron-variant | PPWD1 | GRCh38.p7 | 5:65581028 | GTTAGGAAATGACTA[C/T]AGCATTACAGTATAT | 23398 |
| rs37338 | snp | A/T | 0.487809 | 0.0771174 | intron-variant | PPWD1 | GRCh38.p7 | 5:65581164 | TCTAAATGGGTAAAT[A/T]CTTTTAAGATGAGAA | 23398 |
| rs37339 | snp | A/G | 0.487809 | 0.0771174 | intron-variant | PPWD1 | GRCh38.p7 | 5:65582076 | ACTGGAGAATAGGAT[A/G]TTAAGGTGATAGCAT | 23398 |
| rs37340 | snp | C/T | 0.487684 | 0.0775019 | intron-variant | PPWD1 | GRCh38.p7 | 5:65583775 | GCAACACGGCAAGAC[C/T]CTATCTCTTAAAAAA | 23398 |
| rs41353 | snp | C/T | 0.487809 | 0.0771174 | intron-variant | PPWD1 | GRCh38.p7 | 5:65577317 | TTGTTAAAAAAAACA[C/T]ACAACAACTTGAAAC | 23398 |
| rs41354 | snp | G/T | 0.487809 | 0.0771174 | intron-variant | PPWD1 | GRCh38.p7 | 5:65578229 | ggatgtaccacagtt[G/T]atccattcacgtact | 23398 |
| rs149208 | snp | A/G | 0.473359 | 0.112298 | intron-variant | PPWD1 | GRCh38.p7 | 5:65569578 | TGCTTTGGGAATACT[A/G]AGTGATTCATAGATC | 23398 |
| rs149512 | snp | A/T | 0.493201 | 0.0579089 | intron-variant | PPWD1 | GRCh38.p7 | 5:65569519 | TAATAGGTTTTTTTT[A/T]AAAAAAAACCCTTCT | 23398 |
| rs149513 | snp | G/T | 0 | 0 | intron-variant | PPWD1 | GRCh38.p7 | 5:65582248 | TAAAGAAACAGGCCT[G/T]GAGAAGTCCAGAGTT | 23398 |
| rs151717 | snp | G/T | 0 | 0 | intron-variant | PPWD1 | GRCh38.p7 | 5:65582209 | ACATCAGATAGAGGT[G/T]GCTTAGGAGAGAGCA | 23398 |
| rs152063 | snp | A/C | 0.487809 | 0.0771174 | intron-variant, utr-variant-5-prime | PPWD1 | GRCh38.p7 | 5:65568830 | TTCTAGTCTCAAGTT[A/C]TCAGTGTGGTAAAAC | 23398 |
| rs154946 | snp | A/C/G | 0.408521 | 0.219172 | intron-variant | PPWD1 | GRCh38.p7 | 5:65576468 | AATCGCTTGAACCTA[A/C/G]GAGGCAGACGCTGCA | 23398 |
| rs154948 | snp | A/G | 0.377187 | 0.215229 | intron-variant | PPWD1 | GRCh38.p7 | 5:65575306 | CCTGCAAAATGTGTA[A/G]TCCAGCATCCTAGGC | 23398 |
| rs154949 | snp | A/G | 0.487809 | 0.0771174 | intron-variant | PPWD1 | GRCh38.p7 | 5:65575267 | CTGAGTCTTCTCTCC[A/G]GCAGAAATGATCATT | 23398 |
| rs154950 | snp | A/G | 0.487809 | 0.0771174 | intron-variant, utr-variant-5-prime | PPWD1 | GRCh38.p7 | 5:65568397 | CATTTTAGAGATGAC[A/G]AAACTGAAGTTTAGA | 23398 |
| rs154951 | snp | A/G | 0.487809 | 0.0771174 | intron-variant | PPWD1 | GRCh38.p7 | 5:65569241 | GTTGAATTTTGTTGC[A/G]TATGAAAGTAGTATG | 23398 |
| rs155064 | snp | A/T | 0.468349 | 0.121752 | intron-variant | PPWD1 | GRCh38.p7 | 5:65578301 | acctgtacacagatg[A/T]ttatagcagctttta | 23398 |
| rs173487 | snp | A/C | 0.31357 | 0.241783 | intron-variant | PPWD1 | GRCh38.p7 | 5:65574760 | AGAGATTTGTGCCGG[A/C]CGGGCGCGGTGGCTC | 23398 |
| rs183044 | snp | G/T | 0 | 0 | intron-variant | PPWD1 | GRCh38.p7 | 5:65565976 | CTTTAACATGTTCTT[G/T]GGACATTGGACTGTT | 23398 |
| rs185013 | snp | A/G | 0.487809 | 0.0771174 | intron-variant | PPWD1 | GRCh38.p7 | 5:65574618 | AAATTAGCCGGGCGC[A/G]GTGGCGGGCGCCTGT | 23398 |
| rs185477 | snp | G/T | 0 | 0 | intron-variant | PPWD1 | GRCh38.p7 | 5:65576032 | cagcatatctcagtt[G/T]ggactagccatctat | 23398 |
| rs187409 | snp | A/G | 0.487809 | 0.0771174 | intron-variant | PPWD1 | GRCh38.p7 | 5:65574919 | AATGAGAGTTTGCCA[A/G]AAAAGCCAACCATCA | 23398 |
| rs192189 | snp | A/G | 0.487746 | 0.0773096 | intron-variant | PPWD1 | GRCh38.p7 | 5:65574518 | CGCGATTGAGCCACT[A/G]CAGTCCGCAGTCCGG | 23398 |
| rs193274 | snp | G/T | 0 | 0 | intron-variant | PPWD1 | GRCh38.p7 | 5:65565991 | TGGACATTGGACTGT[G/T]GTATATATTTTCAGA | 23398 |
| rs261247 | snp | A/G | 0.487809 | 0.0771174 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65566375 | TTGGAACTGGGATAT[A/G]ACTGCTGTAATCTTA | 23398 |
| rs261248 | snp | C/T | 0.487809 | 0.0771174 | intron-variant | PPWD1 | GRCh38.p7 | 5:65566101 | GTGGACAAATACTTA[C/T]TAAGAACACAATACG | 23398 |
| rs261249 | snp | A/C | 0.492693 | 0.0882035 | intron-variant | PPWD1 | GRCh38.p7 | 5:65566092 | TACTTACTAAGAACA[A/C]AATACGTTCTAGGTC | 23398 |
| rs261250 | snp | A/G | 0.313814 | 0.241719 | upstream-variant-2KB, intron-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65564720 | AGTAAGGGGTTGGGA[A/G]AGGAAGGTAATGGAA | 23398 |
| rs261251 | snp | A/G | 0.485118 | 0.0849685 | upstream-variant-2KB, intron-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65564275 | AGTTTTTTAAGGGAA[A/G]GTGCTAAAGTACGAT | 23398 |
| rs261252 | snp | A/T | 0.358034 | 0.225452 | upstream-variant-2KB, intron-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65563765 | ACTAACATTTTCCTA[A/T]TCTTATGTGTTTGGC | 23398 |
| rs261253 | snp | C/T | 0.498632 | 0.0261223 | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65561236 | ATTCATGATGACTGA[C/T]TTTGGCTTTGTGAAC | 23398 |
| rs353312 | snp | G/T | 0.0201999 | 0.0984476 | intron-variant | PPWD1 | GRCh38.p7 | 5:65565983 | ATGTTCTTTGGACAT[G/T]GGACTGTTGTATATA | 23398 |
| rs402645 | snp | C/G | 0.499846 | 0.00878459 | upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65563200 | TTGGATGTGCTCATT[C/G]CCACCCCAGCCAATC | 23398 |
| rs432206 | snp | C/G | 0.499928 | 0.00598999 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | CENPK, PPWD1 | GRCh38.p7 | 5:65562860 | GAAAACATGTTTAGT[C/G]CATCTGAAAGGAAAC | 23398 |
| rs433041 | snp | G/T | | | downstream-variant-500B | PPWD1 | GRCh38.p7 | 5:65587883 | ACTTTATCATAGATA[G/T]ATATATATGAAAACA | 23398 |
| rs436185 | snp | A/C | 0 | 0 | intron-variant | PPWD1 | GRCh38.p7 | 5:65573864 | AGTGATGGCTAGAGT[A/C]ACTCTTTCAAAATAT | 23398 |
| rs456564 | snp | A/T | 0.37778 | 0.214877 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65567169 | TTTCATGGAACTTTT[A/T]AATTTTTTTTCCTTT | 23398 |
| rs460262 | snp | G/T | 0.487746 | 0.0773096 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65568005 | ATGAGTAGGTTCGTG[G/T]AGAAGGATAATAATA | 23398 |
| rs461534 | snp | G/T | 0.484841 | 0.0857308 | upstream-variant-2KB, intron-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65564097 | ATACGATGGGCTGAG[G/T]CTTTTTGTCACTAAC | 23398 |
| rs461780 | snp | A/G | 0.487809 | 0.0771174 | intron-variant | PPWD1 | GRCh38.p7 | 5:65574490 | CGGCCTGGGCAACAG[A/G]GCGAGACTCCGTCTC | 23398 |
| rs467362 | snp | C/T | 0.487746 | 0.0773096 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65567861 | GAGTGAACCAGGTAG[C/T]GTCTGAGCTTCCCTG | 23398 |
| rs467436 | snp | A/T | 0.484841 | 0.0857308 | upstream-variant-2KB, intron-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65564099 | ACGATGGGCTGAGTC[A/T]TTTTGTCACTAACGA | 23398 |
| rs468821 | snp | A/G | 0.487809 | 0.0771174 | intron-variant | PPWD1 | GRCh38.p7 | 5:65573797 | TGGAGATAGAATCAT[A/G]AGTTAAAACAGATCA | 23398 |
| rs582627 | snp | C/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65579204 | TGAggccaggcacgg[C/T]ggctcacacctgtaa | 23398 |
| rs626485 | snp | C/T | 0 | 0 | intron-variant | PPWD1 | GRCh38.p7 | 5:65579196 | tgctgggattacagg[C/T]gtgagccaccgtgcc | 23398 |
| rs626503 | snp | C/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65579212 | gtgagccgccgtgcc[C/T]ggccTCATTTCTGTT | 23398 |
| rs669571 | snp | A/G | 0.487933 | 0.0767327 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65566985 | AGGATGTTCTCAGGC[A/G]TAAAAATCTAAGAAT | 23398 |
| rs1309794 | snp | A/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65573554 | ttttttttttttttt[A/T]agtacagacgggttt | 23398 |
| rs1611096 | in-del | -/CAAA | 0.487809 | 0.0771174 | intron-variant | PPWD1 | GRCh38.p7 | 5:65576192 | TCTAGTAACATTAAA[-/CAAA]GTATAAAGAAAACAG | 23398 |
| rs2546061 | snp | C/T | | | | | GRCh38.p7 | 5:65578766 | atatatatgtatata[C/T]atatacacatatatg | 23398 |
| rs3752673 | snp | C/T | 0.367058 | 0.220901 | intron-variant | PPWD1 | GRCh38.p7 | 5:65569831 | AATCATGCACACTTA[C/T]TTTACTGTTATTTAC | 23398 |
| rs3752674 | snp | A/G | 0.0886198 | 0.190936 | intron-variant | PPWD1 | GRCh38.p7 | 5:65570021 | TTTTTAAAAGTATAT[A/G]TATTTTAACTTATTG | 23398 |
| rs3756301 | snp | G/T | 0.293037 | 0.246268 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65567458 | AAATAAACCAAATAC[G/T]ATTTTGTATTTTCTT | 23398 |
| rs6862211 | snp | C/G | 0.145305 | 0.227022 | intron-variant | PPWD1 | GRCh38.p7 | 5:65574751 | TACAGGCGTGAGCCA[C/G]CGCGCCCGGCCGGCA | 23398 |
| rs6867890 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | PPWD1 | GRCh38.p7 | 5:65575573 | TGGGACAGAAGTCTG[A/G]CTTATTTTCATCTGC | 23398 |
| rs6879928 | snp | C/G | 0.0410537 | 0.137264 | intron-variant | PPWD1 | GRCh38.p7 | 5:65570681 | gttccatcagggttt[C/G]atttctgatgagggc | 23398 |
| rs7379716 | snp | A/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65573477 | tatatatatatatat[A/T]ttttttttattagag | 23398 |
| rs9686195 | snp | G/T | 0 | 0 | intron-variant | PPWD1 | GRCh38.p7 | 5:65583991 | CGTAAGGGCTTCAAT[G/T]GAAAAAAAGGTGAAC | 23398 |
| rs9686777 | snp | C/T | | | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65566820 | TCCATCCCTTTCTTT[C/T]TTTTTTTTTTTTTGC | 23398 |
| rs9687917 | snp | A/G | 0 | 0 | intron-variant | PPWD1 | GRCh38.p7 | 5:65583992 | GTAAGGGCTTCAATT[A/G]AAAAAAAGGTGAACA | 23398 |
| rs9790869 | snp | G/T | 0.371987 | 0.218218 | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65562753 | GTCTTTTGGTTATTT[G/T]AAGTAGCTGCTTCTC | 23398 |
| rs9791024 | snp | A/C | 0.370974 | 0.218781 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65563128 | AACTCCAGGTCGCCT[A/C]GGCGCTGCGCAGGAA | 23398 |
| rs9885586 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant, utr-variant-5-prime | PPWD1 | GRCh38.p7 | 5:65568694 | ggtggattACTTTAC[A/G]CTTTTTTAGATCAGT | 23398 |
| rs10053248 | snp | A/T | 0 | 0 | intron-variant | PPWD1 | GRCh38.p7 | 5:65579231 | CTCATTTCTGTTTTT[A/T]AACCTGAAAATTATA | 23398 |
| rs10514984 | snp | A/G | 0.124837 | 0.216412 | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65562553 | CAAATACAGCTTGTC[A/G]AAATGACCTCCGTAA | 23398 |
| rs10560318 | in-del | -/ACAC | | | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65561616 | CACACACACACACAC[-/ACAC]TTAAGAGTTGAACTT | 23398 |
| rs10592952 | in-del | -/GG | | | upstream-variant-2KB, intron-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65564061 | AAACCCGAAGTCTGT[-/GG]TTTTGAAATCACGCT | 23398 |
| rs10682457 | in-del | -/A/AA | 0.5 | 0 | intron-variant | PPWD1 | GRCh38.p7 | 5:65584889 | TATGAAAAAAAAAAA[-/A/AA]CAACTGTCCTTCTGA | 23398 |
| rs10940044 | snp | A/G | 0.438105 | 0.164671 | intron-variant | PPWD1 | GRCh38.p7 | 5:65578808 | tatacatatatatgt[A/G]tatatatatactttt | 23398 |
| rs11282501 | in-del | -/TGTTAA | 0.473543 | 0.111932 | intron-variant | PPWD1 | GRCh38.p7 | 5:65576119 | CTCAATTTTTTATAT[-/TGTTAA]TGTTGAGATGATATT | 23398 |
| rs11740053 | snp | A/G | 0.369754 | 0.219451 | intron-variant | PPWD1 | GRCh38.p7 | 5:65581787 | AGCTTTATACAGCTA[A/G]CATTGTTACGAATTT | 23398 |
| rs11743237 | snp | C/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65573324 | taattaatttatttt[C/T]tgagacagagttgca | 23398 |
| rs11952433 | snp | C/T | 0.145305 | 0.227022 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65566692 | TACATATAATTCTCC[C/T]CTCCCCTCGTTCCCT | 23398 |
| rs11957149 | snp | A/G | 0.145305 | 0.227022 | upstream-variant-2KB, intron-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65564841 | GAATAATTTCCCTCA[A/G]CTCTTCCACTGAACT | 23398 |
| rs11959161 | snp | G/T | 0.145305 | 0.227022 | intron-variant | PPWD1 | GRCh38.p7 | 5:65581215 | ATTATTACTAAAAAT[G/T]TATTAGTATATGAAG | 23398 |
| rs12516229 | snp | C/G | 0.36955 | 0.219562 | intron-variant | PPWD1 | GRCh38.p7 | 5:65565444 | TAAACTTAATATAAC[C/G]GAGACAGATATAAAT | 23398 |
| rs12520386 | snp | C/T | 0 | 0 | intron-variant | PPWD1 | GRCh38.p7 | 5:65576674 | gccaccatgcccagc[C/T]TGAAATACTATTTTT | 23398 |
| rs12652387 | snp | A/G | 0 | 0 | downstream-variant-500B | PPWD1 | GRCh38.p7 | 5:65587614 | AATGGACTAAACTCA[A/G]GCAAATAGCACTCAT | 23398 |
| rs13160139 | snp | A/G | 0.00472811 | 0.0483911 | intron-variant | PPWD1 | GRCh38.p7 | 5:65580999 | TATGTCTTCTTCACT[A/G]TTAAATCCAGAAAGT | 23398 |
| rs13161135 | snp | C/T | 0.118933 | 0.212888 | intron-variant | PPWD1 | GRCh38.p7 | 5:65575822 | ACCTAATGGTAATCT[C/T]ACTGCCCTGTGTCAG | 23398 |
| rs13167170 | snp | A/C | 0 | 0 | missense, intron-variant, utr-variant-5-prime | PPWD1 | GRCh38.p7 | 5:65569983 | ACTTTGACATGATCA[A/C]CATGCTGAAACTTGG | 23398 |
| rs13167188 | snp | A/C | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65570029 | AGTATATATATTTTA[A/C]CTTATTGAAGTAATT | 23398 |
| rs13167303 | snp | A/C | 0 | 0 | intron-variant | PPWD1 | GRCh38.p7 | 5:65570060 | TGTAAATCAGACTTT[A/C]CCATTTAATAGGTTA | 23398 |
| rs13167451 | snp | A/C | 0.118584 | 0.212673 | intron-variant | PPWD1 | GRCh38.p7 | 5:65570094 | CTAAATAGTATATTA[A/C]CATATCTTTAAATAA | 23398 |
| rs13167480 | snp | A/C | 0 | 0 | intron-variant | PPWD1 | GRCh38.p7 | 5:65570210 | CACAGAAATTTCTAA[A/C]CAGCATCATAACAAG | 23398 |
| rs13167526 | snp | C/G | 0 | 0 | missense, intron-variant, utr-variant-5-prime | PPWD1 | GRCh38.p7 | 5:65569943 | GTGGGTGATGATAAA[C/G]CAATGAAGGTGTTTG | 23398 |
| rs13177756 | snp | A/G | 0.293037 | 0.246268 | intron-variant | PPWD1 | GRCh38.p7 | 5:65579177 | CTGCCTCGGCCTCCC[A/G]AAGTGCTGGGATTAC | 23398 |
| rs13187337 | snp | G/T | | | synonymous-codon, intron-variant, utr-variant-5-prime | PPWD1 | GRCh38.p7 | 5:65569996 | CAACATGCTGAAACT[G/T]GGGTGAGTCTTTTTA | 23398 |
| rs13187647 | snp | G/T | 0 | 0 | intron-variant | PPWD1 | GRCh38.p7 | 5:65570185 | GCATCTGCTATGATT[G/T]GTTATCAATCACAGA | 23398 |
| rs13435940 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | PPWD1 | GRCh38.p7 | 5:65578376 | acaattgctggatca[G/T]atggtaacagaatgt | 23398 |
| rs13436616 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | PPWD1 | GRCh38.p7 | 5:65576632 | cacctgccttggcct[A/C]ccaaaatgctgggat | 23398 |
| rs16893963 | snp | A/G | 0.140242 | 0.224618 | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65562488 | AGAGATTTACGACGA[A/G]GATTTTATTAGGTTG | 23398 |
| rs16893969 | snp | A/C | 0.29432 | 0.24604 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | CENPK, PPWD1 | GRCh38.p7 | 5:65563062 | GAGCTCCACAAGATT[A/C]AACCGTTATATCAAC | 23398 |
| rs16894005 | snp | A/C | 0.293037 | 0.246268 | intron-variant | PPWD1 | GRCh38.p7 | 5:65574860 | GATTAGCCTGAGGTG[A/C]CAAGAAGTCAGTAGT | 23398 |
| rs16894025 | snp | C/T | 0.0185238 | 0.0944393 | intron-variant | PPWD1 | GRCh38.p7 | 5:65587213 | TATAATTTAAAGAAA[C/T]TGGGGTTTACCAAGA | 23398 |
| rs17233185 | snp | A/G | 0.0621006 | 0.164908 | intron-variant | PPWD1 | GRCh38.p7 | 5:65576870 | GTTACTAAATGGTTT[A/G]TTTCCTAGATGTTTA | 23398 |
| rs33916564 | in-del | -/TA | 0 | 0 | intron-variant | PPWD1 | GRCh38.p7 | 5:65575660 | GTAAAGATCGTTACT[-/TA]CTTTTGGAAGGTTCA | 23398 |
| rs33959203 | in-del | -/A | 0.489023 | 0.0780865 | intron-variant | PPWD1 | GRCh38.p7 | 5:65579231 | TCATTTCTGTTTTTT[-/A]AACCTGAAAATTATA | 23398 |
| rs34035956 | in-del | -/A | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65579645 | GAGATTAGACGGTAA[-/A]TGTTCCTTCCAGTTT | 23398 |
| rs34166309 | in-del | -/G | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65577668 | AGTTAACAGACATGG[-/G]AATTTTAATAAGAAT | 23398 |
| rs34185044 | in-del | -/C | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65576233 | AATTACCTATGTGGC[-/C]TTGTGTTATATTTCA | 23398 |
| rs34288822 | in-del | -/T | 0.487809 | 0.0771174 | intron-variant | PPWD1 | GRCh38.p7 | 5:65573189 | CCCTCCCTCCTCATA[-/T]TCCTCCATTACCTAT | 23398 |
| rs34299614 | in-del | -/T | | | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65566638 | TTTAGCAACTTTTTT[-/T]AGGCACGTTTGGTCA | 23398 |
| rs34727801 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | PPWD1 | GRCh38.p7 | 5:65584504 | AGAAAATGACCTTTC[C/T]CAGGAACTTAACCTA | 23398 |
| rs34898359 | in-del | -/A | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65585974 | AAAAGGACAATGTAA[-/A]TGTTTTTGTGTACTT | 23398 |
| rs35080676 | in-del | -/A | 0.5 | 0 | intron-variant | PPWD1 | GRCh38.p7 | 5:65565808 | AAAAAAAAAAAAAAA[-/A]GCCAATAGTTTATTC | 23398 |
| rs35113726 | in-del | -/GA/GATA | | | downstream-variant-500B | PPWD1 | GRCh38.p7 | 5:65587882 | ACTTTATCATAGATA[-/GA/GATA]TATATATATGAAAAC | 23398 |
| rs35266780 | in-del | -/CACA | | | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65561605 | TAATTAAAACACACA[-/CACA]CACACACACACTTAA | 23398 |
| rs35314610 | in-del | -/A | 0.487809 | 0.0771174 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65568080 | AGTTTTTGAGTGCTG[-/A]ACATGATACTCAAAA | 23398 |
| rs35326591 | in-del | -/TG | 0.48491 | 0.0855403 | upstream-variant-2KB, intron-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65564058 | CCAAAACCCGAAGTC[-/TG]TGGTTTTGAAATCAC | 23398 |
| rs35350988 | in-del | -/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65572400 | ATAGACTTATTTTTT[-/T]CTTAGCACATTAGAG | 23398 |
| rs35368186 | in-del | -/T | 0.487933 | 0.0767327 | intron-variant | PPWD1 | GRCh38.p7 | 5:65585862 | ATCCAAATTTAAGTG[-/T]TAAGGGTTTAATCAA | 23398 |
| rs35437959 | in-del | -/C | | | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65568188 | AGAAATTGAAACTCC[-/C]AAAACACTTCTGGTC | 23398 |
| rs35506525 | in-del | -/T | 0.122064 | 0.214785 | intron-variant | PPWD1 | GRCh38.p7 | 5:65583743 | GGAGGCCAGCAGTTT[-/T]GAGACTAGCCCGAGC | 23398 |
| rs35529383 | in-del | -/A | 0.5 | 0 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65567658 | TTAAAAAAAAAAAAA[-/A]GCTTCAATTTTGAGG | 23398 |
| rs35782298 | in-del | -/CTTT | 0.302184 | 0.244493 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65566812 | TCATTCTCTCCATCC[-/CTTT]CTTTCTTTTTTTTTT | 23398 |
| rs35830400 | snp | C/T | 1.66821e-05 | 0.00288804 | upstream-variant-2KB, utr-variant-5-prime, missense | CENPK, PPWD1 | GRCh38.p7 | 5:65563324 | TGAAAATCGCTACCA[C/T]TTTCCGCCGCCATGT | 23398 |
| rs35938430 | in-del | -/GA | | | downstream-variant-500B | PPWD1 | GRCh38.p7 | 5:65587884 | TTTATCATAGATATA[-/GA]TATATATGAAAACAC | 23398 |
| rs35984619 | snp | A/G | 0.145305 | 0.227022 | upstream-variant-2KB, intron-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65564062 | AACCCGAAGTCTGTG[A/G]TTTTGAAATCACGCT | 23398 |
| rs41268429 | snp | A/G | 0.0271762 | 0.113356 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65563113 | CATCACAGCGTCACA[A/G]ACTCCAGGTCGCCTA | 23398 |
| rs41268431 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | CENPK, PPWD1 | GRCh38.p7 | 5:65563292 | TTTGTGTCGCGCCTT[C/T]TCTGACGATGCGAAC | 23398 |
| rs55841350 | snp | A/G | 0.122758 | 0.215196 | intron-variant | PPWD1 | GRCh38.p7 | 5:65572783 | GTGTAATTCACTGGA[A/G]TCCTGCCAATTTTGC | 23398 |
| rs56156711 | snp | A/C | 0.00364648 | 0.0425434 | utr-variant-3-prime | PPWD1 | GRCh38.p7 | 5:65587424 | TTTAATGTACTTGCA[A/C]ATAAAAATACAATAT | 23398 |
| rs56227785 | snp | C/T | 0.0298908 | 0.118541 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65567493 | AAAATAGATCTTATA[C/T]TTTACTTTTTTTTCT | 23398 |
| rs57517399 | snp | G/T | 0.0633504 | 0.166319 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65566701 | TTCTCCCCTCCCCTC[G/T]TTCCCTCCTTCCTTC | 23398 |
| rs57811880 | in-del | -/GTTT | 0.375 | 0.216506 | intron-variant | PPWD1 | GRCh38.p7 | 5:65576195 | TTTTCTTTATACTTT[-/GTTT]AATGTTACTAGACAC | 23398 |
| rs58584619 | snp | A/G | 0.0633504 | 0.166319 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65568205 | AAACACTTCTGGTCC[A/G]ATACATTTTGGATAA | 23398 |
| rs60223278 | snp | A/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65573473 | AATATATATATATAT[A/T]TATTTTTTTTTTATT | 23398 |
| rs60858693 | in-del | -/TACTT | 0.498774 | 0.02473 | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65561776 | TTAGGGATAATACTA[-/TACTT]AAAGAAACTCGTACT | 23398 |
| rs61014228 | in-del | -/A | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65565826 | AAAAAAAAAAAAAAA[-/A]GCCAATAGTTTATTC | 23398 |
| rs61174447 | in-del | -/AATGTT | 0.5 | 0 | intron-variant | PPWD1 | GRCh38.p7 | 5:65576123 | ATTTTTTATATTGTT[-/AATGTT]GAGATGATATTCTGG | 23398 |
| rs61548816 | snp | A/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65573475 | TATATATATATATAT[A/T]TTTTTTTTTTATTAG | 23398 |
| rs62369038 | snp | A/T | | | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65567655 | TTTGTTCTGAGTTTA[A/T]TTAAAAAAAAAAAAA | 23398 |
| rs62369039 | snp | A/G | 0.124144 | 0.21601 | intron-variant | PPWD1 | GRCh38.p7 | 5:65581847 | AGCAAAACTAAAATG[A/G]TATGCATATATATGA | 23398 |
| rs62369040 | snp | A/G | 0.369754 | 0.219451 | intron-variant | PPWD1 | GRCh38.p7 | 5:65583442 | TTACGAGGACAAAAT[A/G]TATTGGCTATGAAAG | 23398 |
| rs62369041 | snp | G/T | 0.0248432 | 0.108648 | intron-variant | PPWD1 | GRCh38.p7 | 5:65584031 | GACAGTTTAAAAGAC[G/T]GTAAAATTAACATAC | 23398 |
| rs62369042 | snp | A/G | 0.124144 | 0.21601 | intron-variant | PPWD1 | GRCh38.p7 | 5:65584062 | AATGTCAAATACAGT[A/G]GAGTATCTCTGGCCA | 23398 |
| rs71590871 | in-del | ATATA/CTATCTATC | 0.5 | 0 | downstream-variant-500B | PPWD1 | GRCh38.p7 | 5:65587887 | ATTGTGTTTTCATAT[ATATA/CTATCTATC]TATCTATGATAAAGT | 23398 |
| rs71590872 | multinucleotide-polymorphism | AGA/TGC | 0.5 | 0 | upstream-variant-2KB, intron-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65564097 | TCGTTAGTGACAAAA[AGA/TGC]CTCAGCCCATCGTAT | 23398 |
| rs71608597 | in-del | -/CACTTCT | 0.5 | 0 | upstream-variant-2KB, intron-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65563632 | AGAGGGCCGTCCTCT[-/CACTTCT]GGCTACTCCATACTT | 23398 |
| rs71626585 | snp | A/G | 0.145305 | 0.227022 | intron-variant | PPWD1 | GRCh38.p7 | 5:65581703 | CAAGTTTACTTGTGT[A/G]TTGATCAAAGTATAT | 23398 |
| rs71720962 | in-del | -/AC | | | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65561598 | AGTTGTTTAATTAAA[-/AC]ACACACACACACACA | 23398 |
| rs71728896 | in-del | -/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65573476 | ATATATATATATATA[-/T]TTTTTTTTTATTAGA | 23398 |
| rs71733489 | in-del | -/ACAC | 0.499998 | 0.000998888 | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65561598 | AGTTGTTTAATTAAA[-/ACAC]ACACACACACACACA | 23398 |
| rs72762442 | snp | A/T | 0.0279361 | 0.114837 | upstream-variant-2KB, utr-variant-5-prime | CENPK, PPWD1 | GRCh38.p7 | 5:65563283 | TAGCTGAGTTTTGTG[A/T]CGCGCCTTTTCTGAC | 23398 |
| rs72762449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65573952 | ATCCATGCAGTTAAG[C/T]GGTTTCTGTGATTGC | 23398 |
| rs72762452 | snp | C/T | 0.293294 | 0.246223 | intron-variant | PPWD1 | GRCh38.p7 | 5:65584405 | AGTGTGATTGTCATT[C/T]AAAGTTGAATAAATT | 23398 |
| rs73097124 | snp | G/T | 0.0193772 | 0.0965046 | intron-variant | PPWD1 | GRCh38.p7 | 5:65578893 | CTCCTAGTCTGTGAC[G/T]TTTCATTCTCTTGAT | 23398 |
| rs73097133 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | PPWD1 | GRCh38.p7 | 5:65582724 | GCCTTACTAGAAGGC[A/G]TAAGTCGAGAGCTAC | 23398 |
| rs73097134 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | PPWD1 | GRCh38.p7 | 5:65586941 | AGTCCTCCAGAGACC[G/T]TTTAAAGCCTTAGCC | 23398 |
| rs73762029 | snp | A/G | 0.0134861 | 0.0810011 | upstream-variant-2KB, intron-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65564162 | GGTGGGAAAAGGGGT[A/G]GATTAAGTTTTCTTG | 23398 |
| rs73762030 | snp | A/G | 0.00315662 | 0.0396023 | intron-variant, utr-variant-5-prime | PPWD1 | GRCh38.p7 | 5:65568921 | TTTTAACCCAAGACA[A/G]TGGAAGGTAATACAG | 23398 |
| rs73762031 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | PPWD1 | GRCh38.p7 | 5:65574908 | TGGAGATTCAGAATG[A/G]GAGTTTGCCAAAAAA | 23398 |
| rs73762034 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | PPWD1 | GRCh38.p7 | 5:65584000 | TTCAATTGAAAAAAA[C/G]GTGAACAGTTTTCTG | 23398 |
| rs74323754 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PPWD1 | GRCh38.p7 | 5:65581777 | CATTCACTGTAGCTT[C/T]ATACAGCTAACATTG | 23398 |
| rs74486856 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PPWD1 | GRCh38.p7 | 5:65575020 | AGTTTCTAACCAGTC[A/G]GAATCCTAGTTTAAC | 23398 |
| rs74522791 | snp | G/T | 0.030665 | 0.119967 | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65562078 | TATCGGAATTCAGGA[G/T]AGGGAAGCTTAGAAA | 23398 |
| rs74821527 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | PPWD1 | GRCh38.p7 | 5:65585589 | CTGGCAGGTCAGAAA[C/T]GGCAGGATGAAAAGT | 23398 |
| rs75035255 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | PPWD1 | GRCh38.p7 | 5:65573098 | TATTCTGCCATTTGG[A/G]TCTTCTTTTTATTTC | 23398 |
| rs75955888 | snp | C/T | 0.0165278 | 0.0893908 | upstream-variant-2KB, intron-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65564690 | TGTGATCTCTCCTTA[C/T]CTTCTTAGTGCATCT | 23398 |
| rs76149995 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65561363 | ACATGTGGTGGGGGC[A/G]GAGGGTGAGGGATAA | 23398 |
| rs76499623 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65568308 | TTTTTCTTTTTTTAT[C/G]TATCAAGTTAAGGCT | 23398 |
| rs76522830 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65567293 | ATAGTACCTGGGAAC[C/T]TGTTGTAACTGACTA | 23398 |
| rs77226014 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | PPWD1 | GRCh38.p7 | 5:65580672 | GTGCATGCCACCATA[A/C]CCAGCTAATTTTTGT | 23398 |
| rs77407636 | snp | G/T | 0 | 0 | intron-variant | PPWD1 | GRCh38.p7 | 5:65576393 | TTTTTTTTTTTTTTT[G/T]TGAGACGGAGTCTCA | 23398 |
| rs77418804 | snp | A/T | 0.0271762 | 0.113356 | intron-variant | PPWD1 | GRCh38.p7 | 5:65583793 | ATCTCTTAAAAAAAA[A/T]TTTTTTTTATTAGCT | 23398 |
| rs77792975 | snp | A/G | 0.0654984 | 0.168698 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65566995 | CAGGCATAAAAATCT[A/G]AGAATTTTACCATGT | 23398 |
| rs77871646 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65567864 | TGAACCAGGTAGTGT[C/G]TGAGCTTCCCTGAAG | 23398 |
| rs77905211 | snp | C/T | 0.5 | 0 | intron-variant | PPWD1 | GRCh38.p7 | 5:65578227 | CTGGATGTACCACAG[C/T]TGATCCATTCACGTA | 23398 |
| rs78139171 | in-del | -/G | 0.124144 | 0.21601 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65566493 | TTAAACCTCACTCCA[-/G]GGGAAAGTGAGAAAG | 23398 |
| rs78347381 | snp | A/G | 0.00153771 | 0.0276856 | synonymous-codon | PPWD1 | GRCh38.p7 | 5:65586133 | CAGCATGGCTAACGC[A/G]GGATCAAATACTAAT | 23398 |
| rs78461669 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | PPWD1 | GRCh38.p7 | 5:65569430 | AGGTTAAAATTAGTA[C/T]AGCTGTAACTGTTTT | 23398 |
| rs78541021 | in-del | -/TA | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65584967 | AAAGAAAACTGTTTT[-/TA]AAGATGCTCTGAATA | 23398 |
| rs78680827 | snp | A/G | 0.0633504 | 0.166319 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65567147 | GTTAGGAAGATGGTT[A/G]TGATATTTTCATGGA | 23398 |
| rs78959580 | snp | C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65563739 | ATTGATTTGTTATGA[C/T]AGATGCTAAAACTAA | 23398 |
| rs79028000 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PPWD1 | GRCh38.p7 | 5:65582554 | TCTATTCGTTTAATC[C/T]TCACAACTACCTTCA | 23398 |
| rs79162079 | snp | G/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65572525 | TTTTGTGGTTATTTT[G/T]TTTTTTACAATTTTG | 23398 |
| rs79453219 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | PPWD1 | GRCh38.p7 | 5:65578910 | TTCATTCTCTTGATT[G/T]GTTTTTTGTTGTTGT | 23398 |
| rs79617186 | snp | A/G | 0.0633504 | 0.166319 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65567747 | TAAGTTCTGAAATAA[A/G]GGCCTACATGTTCTT | 23398 |
| rs80052296 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65566773 | TTTCTTTCCCTCCCT[C/T]CTTTCCTTCCTTACT | 23398 |
| rs111378493 | snp | C/T | 0.5 | 0 | missense, intron-variant | PPWD1 | GRCh38.p7 | 5:65571870 | TGTGAGTGGATCTAT[C/T]GCCCAGGGGATGCAA | 23398 |
| rs111380349 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65561701 | AAGTCAACTTTTTGA[A/G]GTCCCCAGTTAGGAC | 23398 |
| rs111597124 | snp | A/G | 0.5 | 0 | missense, intron-variant | PPWD1 | GRCh38.p7 | 5:65571915 | GCTTCCGAAAAGAGT[A/G]CAGGAAAAATTTTCA | 23398 |
| rs111602386 | snp | A/G | 0.5 | 0 | intron-variant | PPWD1 | GRCh38.p7 | 5:65569493 | GTTCTGTAATATAGT[A/G]GTCTGCTTAAAGAAG | 23398 |
| rs111647065 | snp | A/G | 1.64838e-05 | 0.00287083 | upstream-variant-2KB, utr-variant-5-prime, missense | CENPK, PPWD1 | GRCh38.p7 | 5:65563369 | GGCGCCGGGACCCGG[A/G]GGAACCGGAAAAAAC | 23398 |
| rs111670321 | snp | A/T | 0 | 0 | intron-variant | PPWD1 | GRCh38.p7 | 5:65585863 | TCCAAATTTAAGTGT[A/T]AAGGGTTTAATCAAA | 23398 |
| rs111987815 | snp | C/T | 0.5 | 0 | intron-variant | PPWD1 | GRCh38.p7 | 5:65569740 | TCACCTGGGTAAGAA[C/T]TGCACCTCATTTTCT | 23398 |
| rs112157965 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65563232 | CGAAACTCGCTCGGA[C/T]GCTGACAGAAGACTG | 23398 |
| rs112168183 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65566435 | ACACTTTTTCAAGAC[C/T]TCCTGTGACAAAACA | 23398 |
| rs112312468 | snp | C/T | 0.5 | 0 | intron-variant | PPWD1 | GRCh38.p7 | 5:65580530 | AGCCCCTCTGTTTTT[C/T]GGAGATGGCATCTTG | 23398 |
| rs112333661 | in-del | -/AC/ACAC | 0.5 | 0 | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65561597 | AGTTGTTTAATTAAA[-/AC/ACAC]ACACACACACACACA | 23398 |
| rs113057113 | snp | C/T | 0.293294 | 0.246223 | intron-variant | PPWD1 | GRCh38.p7 | 5:65574479 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCGCCCTGT | 23398 |
| rs113457060 | snp | C/T | 0.5 | 0 | missense, intron-variant | PPWD1 | GRCh38.p7 | 5:65572080 | TGGACTGGGCCTCCT[C/T]ATGAATATAAATTCC | 23398 |
| rs113550012 | snp | C/T | 0.00308135 | 0.0391303 | intron-variant | PPWD1 | GRCh38.p7 | 5:65572309 | TAATTTAAATTTAAC[C/T]GTACTTTACTTTTCT | 23398 |
| rs113647368 | in-del | -/A | 0.498206 | 0.0298983 | intron-variant | PPWD1 | GRCh38.p7 | 5:65578741 | TATATATACATATAT[-/A]ATATACACACATATA | 23398 |
| rs113654962 | snp | A/G | 0.0240643 | 0.107019 | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65561270 | AGAATATTTTTAAGC[A/G]AAAAAGTCAAACATA | 23398 |
| rs113671119 | snp | C/T | 0.5 | 0 | intron-variant | PPWD1 | GRCh38.p7 | 5:65583527 | CAGCACATCTGAACT[C/T]TAGGTTTTGTGGATT | 23398 |
| rs113731323 | snp | A/G | 0.5 | 0 | missense, intron-variant | PPWD1 | GRCh38.p7 | 5:65572138 | CTGACACTGATTTAT[A/G]TGAATTTGCCAAGTG | 23398 |
| rs113927963 | snp | C/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65563686 | AGTGATTTAAGCGTA[C/G]TACAACGTCTTTTTG | 23398 |
| rs113948527 | in-del | -/TCTCACT | 0.118584 | 0.212673 | upstream-variant-2KB, intron-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65563629 | AACAGAGGGCCGTCC[-/TCTCACT]TCTGGCTACTCCATA | 23398 |
| rs114625836 | snp | A/G | 0.031825 | 0.122064 | intron-variant | PPWD1 | GRCh38.p7 | 5:65578988 | CAGTGGCACGATCTC[A/G]GCTCACAACCTCTGC | 23398 |
| rs114746088 | snp | A/G | 0.0199929 | 0.0979629 | upstream-variant-2KB, intron-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65563516 | GGAAAGGTAGCTGCA[A/G]ACATAGTACCGGGAC | 23398 |
| rs114773980 | snp | C/G/T | 3.39843e-05 | 0.00412204 | missense | PPWD1 | GRCh38.p7 | 5:65579456 | GCAAACAAGAAAATA[C/G/T]TAGAGTGATGCAATT | 23398 |
| rs114802254 | snp | A/G | 0.030665 | 0.119967 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65566376 | AAGATTACAGCAGTT[A/G]TATCCCAGTTCCAAG | 23398 |
| rs114978224 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | PPWD1 | GRCh38.p7 | 5:65578830 | TATACTTTTTTTTAA[A/G]AAAAGAGTTTTTTAT | 23398 |
| rs115121054 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PPWD1 | GRCh38.p7 | 5:65585286 | TCAACAGGAATAGTG[C/G]CATGATTAGAAACAC | 23398 |
| rs115183228 | snp | G/T | 0.0414363 | 0.137845 | intron-variant | PPWD1 | GRCh38.p7 | 5:65578835 | TTTTTTTTAAAAAAA[G/T]AGTTTTTTATATATT | 23398 |
| rs115861927 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | PPWD1 | GRCh38.p7 | 5:65572705 | CTTCATAAATGGTGC[C/T]AGTATCCATCTAGTT | 23398 |
| rs116164471 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPWD1 | GRCh38.p7 | 5:65572941 | CCACTCTGCACCCAG[A/G]GCCATCTTTTACAAG | 23398 |
| rs116309955 | snp | A/G | 0.030278 | 0.119257 | intron-variant | PPWD1 | GRCh38.p7 | 5:65579077 | CCTGCCACCATGCTT[A/G]ACCAATTTCTTGTAT | 23398 |
| rs116490485 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | PPWD1 | GRCh38.p7 | 5:65583944 | GCAACAGAGTGAGAC[C/T]CTGTTTCTACAAAAA | 23398 |
| rs116518522 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65562073 | AGTACTATCGGAATT[A/C]AGGATAGGGAAGCTT | 23398 |
| rs116705554 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | PPWD1 | GRCh38.p7 | 5:65565882 | AAAAACATACATAGA[A/G]TGTTACAAAAATATT | 23398 |
| rs116792697 | snp | C/G/T | 0.00749765 | 0.0607676 | upstream-variant-2KB, utr-variant-5-prime | CENPK, PPWD1 | GRCh38.p7 | 5:65563301 | CGCCTTTTCTGACGA[C/G/T]GCGAACAACATGGCG | 23398 |
| rs137860782 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | CENPK, PPWD1 | GRCh38.p7 | 5:65563074 | ATTCAACCGTTATAT[C/T]AACCTCCCCGGCCCA | 23398 |
| rs137980566 | snp | G/T | 6.62756e-05 | 0.00575616 | synonymous-codon, intron-variant | PPWD1 | GRCh38.p7 | 5:65572205 | TGGGAAGAAAATAGC[G/T]ACTATTGGTTCTGAT | 23398 |
| rs138014576 | snp | A/G | 0.00231794 | 0.0339647 | intron-variant | PPWD1 | GRCh38.p7 | 5:65569775 | GCTCTTTCCTAAACT[A/G]TACTAATTAAAGTTT | 23398 |
| rs138162640 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPWD1 | GRCh38.p7 | 5:65582190 | ACGTTCCCATAATTA[A/G]GTTACATCAGATAGA | 23398 |
| rs138491031 | snp | G/T | 1.65228e-05 | 0.00287422 | missense, intron-variant | PPWD1 | GRCh38.p7 | 5:65572146 | GATTTATATGAATTT[G/T]CCAAGTGTAAGGCTT | 23398 |
| rs138622467 | snp | A/G | 0.00123663 | 0.0248352 | upstream-variant-2KB, utr-variant-5-prime, missense | CENPK, PPWD1 | GRCh38.p7 | 5:65563407 | AGCGAAAGAGAGCTG[A/G]CAGTAGCAGTGGCGG | 23398 |
| rs138676513 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PPWD1 | GRCh38.p7 | 5:65578076 | TTGCCTCTTCCAGAA[C/T]GTGATATAGCTAAAA | 23398 |
| rs138848281 | snp | A/G | 0 | 0 | intron-variant | PPWD1 | GRCh38.p7 | 5:65577681 | TGGAATTTTAATAAG[A/G]ATAGGTTAAAACTGT | 23398 |
| rs138922075 | snp | A/C/T | 3.33953e-05 | 0.00408616 | missense | PPWD1 | GRCh38.p7 | 5:65583201 | TGGGAGACATTCACA[A/C/T]CAAACTTTTTCCTGT | 23398 |
| rs138927551 | snp | A/G | 0.0562307 | 0.157967 | intron-variant | PPWD1 | GRCh38.p7 | 5:65573629 | TCTGCCTGCCTTGGC[A/G]TCCCAAAGTGCTGGG | 23398 |
| rs139036667 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPWD1 | GRCh38.p7 | 5:65580272 | TTTTAAGACCCAAAC[A/G]TGACTCTTATTTTCT | 23398 |
| rs139357508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65574025 | ATTGAACCTTTGTAG[C/T]AAAGTTTATTGTATG | 23398 |
| rs139525347 | in-del | -/ATAG/ATAGATAG | 0.333261 | 0.235728 | downstream-variant-500B | PPWD1 | GRCh38.p7 | 5:65587875 | AAATTAAACTTTATC[-/ATAG/ATAGATAG]ATAGATATATATATA | 23398 |
| rs139664723 | snp | G/T | 0.000825696 | 0.0203019 | missense | PPWD1 | GRCh38.p7 | 5:65587328 | CAGAGGATCTCCAAC[G/T]TCAAAGTCAATCCCA | 23398 |
| rs139695220 | snp | A/C | 4.95421e-05 | 0.00497681 | synonymous-codon | PPWD1 | GRCh38.p7 | 5:65587286 | CATACAGTATTTGGA[A/C]GAGTGACTAAAGGAA | 23398 |
| rs139866806 | snp | A/G | 0.00517822 | 0.0506191 | upstream-variant-2KB, intron-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65564886 | CTTTAGCACTTAGCT[A/G]TCATCTTCTCTGGGA | 23398 |
| rs140167706 | snp | A/G | 0.000185856 | 0.00963813 | intron-variant, missense | PPWD1 | GRCh38.p7 | 5:65568984 | AGCCACTCTAGCTAT[A/G]TGGACCTGAGGCAAG | 23398 |
| rs140196698 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PPWD1 | GRCh38.p7 | 5:65574512 | CCCAGGCCGGACTGC[A/G]GACTGTAGTGGCTCA | 23398 |
| rs140226001 | snp | C/T | 0.000132183 | 0.0081286 | missense, intron-variant | PPWD1 | GRCh38.p7 | 5:65572152 | TATGAATTTGCCAAG[C/T]GTAAGGCTTATCCAA | 23398 |
| rs140323376 | in-del | -/AATGTT | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65576118 | TCTCAATTTTTTATA[-/AATGTT]TTGTTGAGATGATAT | 23398 |
| rs140438590 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPWD1 | GRCh38.p7 | 5:65582002 | ATATATCAGCTAAGT[C/T]ATAACTTTAAAAAAT | 23398 |
| rs140588547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65562737 | ACCCGTTCTGCCCTA[A/G]GTCTTTTGGTTATTT | 23398 |
| rs140669475 | snp | A/G | 6.59914e-05 | 0.00574381 | missense, intron-variant | PPWD1 | GRCh38.p7 | 5:65571984 | TTTGACAAACTCCAT[A/G]CATCACCTCTTACTC | 23398 |
| rs140790565 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, utr-variant-5-prime | PPWD1 | GRCh38.p7 | 5:65568583 | TGGATTCAAACAGGG[C/T]AAGAATGGATACAGG | 23398 |
| rs140804671 | snp | A/G/T | 0.00755907 | 0.0610114 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65563132 | CCAGGTCGCCTAGGC[A/G/T]CTGCGCAGGAAGCGC | 23398 |
| rs140843173 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PPWD1 | GRCh38.p7 | 5:65565683 | CGTGGTGGCGCACAC[C/T]TATAATCTCAGCTAT | 23398 |
| rs140936095 | in-del | -/C | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65576371 | TACCATTTTGAAATA[-/C]AATTTTTTTTTTTTT | 23398 |
| rs141224482 | snp | A/C | 0.000159461 | 0.00892777 | utr-variant-3-prime | PPWD1 | GRCh38.p7 | 5:65587422 | GTTTTAATGTACTTG[A/C]AAATAAAAATACAAT | 23398 |
| rs141323857 | snp | A/T | 0.00661124 | 0.0571131 | intron-variant | PPWD1 | GRCh38.p7 | 5:65584979 | TTTTAAGATGCTCTG[A/T]ATAGGTTTCATATTT | 23398 |
| rs141336092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65581371 | GCAGAAAGATCATTT[A/G]AGCCCAGGACCAAGA | 23398 |
| rs141493463 | in-del | -/AG | 0.00312384 | 0.0393975 | utr-variant-3-prime | PPWD1 | GRCh38.p7 | 5:65587445 | AATACAATATTAAAC[-/AG]ATTATTTTACATTAG | 23398 |
| rs141770743 | snp | C/T | 0.0352966 | 0.128072 | upstream-variant-2KB, intron-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65564528 | GTTTCACCATGTTGG[C/T]CAGGATGGTCTTGAT | 23398 |
| rs141783054 | in-del | -/TTC | 0.00438332 | 0.0466095 | intron-variant | PPWD1 | GRCh38.p7 | 5:65581826 | TCTTACTAGTACATA[-/TTC]TTAAGCAAAACTAAA | 23398 |
| rs142197442 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | PPWD1 | GRCh38.p7 | 5:65583774 | AGCAACACGGCAAGA[C/T]TCTATCTCTTAAAAA | 23398 |
| rs142403801 | snp | A/G | 0.000614113 | 0.0175123 | missense, intron-variant, utr-variant-5-prime | PPWD1 | GRCh38.p7 | 5:65569660 | ATTACTGCCAGTCAT[A/G]ATGGACATGTCAAGT | 23398 |
| rs142421174 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65562238 | ACATGAAGGCTAAAT[C/T]GCTGTGGAGATGCTT | 23398 |
| rs142524226 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65562132 | CATAATAATGCTTAA[A/T]AAATGTTAACTAGCT | 23398 |
| rs142815878 | snp | A/G | 4.96364e-05 | 0.00498154 | missense | PPWD1 | GRCh38.p7 | 5:65579504 | TAGCCAAAAAGCATC[A/G]TGCTGCAACTACTAT | 23398 |
| rs142829831 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | PPWD1 | GRCh38.p7 | 5:65582429 | TCAGATTCATTTTTG[G/T]GAATCCTTATTCTAC | 23398 |
| rs142855221 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPWD1 | GRCh38.p7 | 5:65577737 | ATAGACCTTACTTTT[C/T]TGAACAGTTTTAGGT | 23398 |
| rs142934675 | snp | C/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65578775 | GTATATATATATACA[C/T]ATATATGTGTATATA | 23398 |
| rs142985211 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | PPWD1 | GRCh38.p7 | 5:65584423 | AGTTGAATAAATTTA[G/T]ATGTCATTTCTATGA | 23398 |
| rs143028276 | in-del | -/TA | 0.487809 | 0.0771174 | intron-variant | PPWD1 | GRCh38.p7 | 5:65575659 | TGTAAAGATCGTTAC[-/TA]TCTTTTGGAAGGTTC | 23398 |
| rs143194443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65587118 | CATTTTTATTGCTGA[A/G]AAATTATTGTACTTC | 23398 |
| rs143475555 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65576020 | ACTGAGCATTTGATA[C/G]ATGGCTAGTCCAAAC | 23398 |
| rs143809868 | snp | C/T | 1.65395e-05 | 0.00287567 | synonymous-codon, intron-variant | PPWD1 | GRCh38.p7 | 5:65571905 | TTCAGTTGCTGCTTC[C/T]GAAAAGAGTACAGGA | 23398 |
| rs143872326 | snp | A/G | | | upstream-variant-2KB, intron-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65564975 | GGTAGTTATATATCA[A/G]TACTGAATTTACAGG | 23398 |
| rs143925012 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | PPWD1 | GRCh38.p7 | 5:65574534 | AGTGGCTCAATCGCG[A/G]CTCACTGCAAGCTCC | 23398 |
| rs143955881 | snp | A/G | 5.28434e-05 | 0.00513993 | missense | PPWD1 | GRCh38.p7 | 5:65579432 | TTTTTAGGTGTGTGC[A/G]GATTTTAGGCAAACA | 23398 |
| rs144256813 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | PPWD1 | GRCh38.p7 | 5:65584586 | ATTGGGCCAGGTACA[A/G]TGGCTCAGGCCTGTA | 23398 |
| rs144320016 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65581127 | ATGAAATAGCAGTTT[C/G]CCTACCCCAACCAAC | 23398 |
| rs144564157 | snp | C/T | 0.0599851 | 0.162463 | upstream-variant-2KB, intron-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65564412 | CGGCTCACCGCAACC[C/T]CCGTCTCCGGGGTTC | 23398 |
| rs144623996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | PPWD1 | GRCh38.p7 | 5:65568808 | TCTGACCAAATATTA[A/G]CACCTTTTCTAGTCT | 23398 |
| rs144631160 | in-del | -/G | 0.00398564 | 0.0444627 | intron-variant | PPWD1 | GRCh38.p7 | 5:65569571 | GTGAATGATTGCTTT[-/G]GGAATACTAAGTGAT | 23398 |
| rs144728024 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPWD1 | GRCh38.p7 | 5:65578240 | AGTTGATCCATTCAC[A/G]TACTGAAAGACATCT | 23398 |
| rs144830174 | snp | A/C/T | 0.00438332 | 0.0466095 | intron-variant | PPWD1 | GRCh38.p7 | 5:65584248 | AACCCATGTACTCTT[A/C/T]GGCCTTGTTTGCTGA | 23398 |
| rs145070580 | snp | A/G | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65585820 | TATGTTTCAATCAAG[A/G]TGGTGGTTGGGCAAT | 23398 |
| rs145240557 | snp | G/T | 1.90217e-05 | 0.00308391 | upstream-variant-2KB, missense, utr-variant-5-prime | CENPK, PPWD1 | GRCh38.p7 | 5:65563489 | CTGTGGAGGCAACAC[G/T]GGCCAAGAAGAGGAA | 23398 |
| rs145356091 | in-del | -/C | 0.0633504 | 0.166319 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65566700 | ATTCTCCCCTCCCCT[-/C]GTTCCCTCCTTCCTT | 23398 |
| rs145372576 | snp | A/G/T | 8.47859e-05 | 0.0065105 | upstream-variant-2KB, missense, utr-variant-5-prime | CENPK, PPWD1 | GRCh38.p7 | 5:65563456 | AGGAGAACGAAGAGC[A/G/T]CTGGGTTGGACCTTT | 23398 |
| rs145410204 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65561244 | AGCCAAAATCAGTCA[A/T]CATGAATTTTAGAAT | 23398 |
| rs145769947 | snp | A/G | 0.00388943 | 0.0439271 | synonymous-codon | PPWD1 | GRCh38.p7 | 5:65587312 | AGGAATGGAAGTTGT[A/G]CAGAGGATCTCCAAC | 23398 |
| rs145794707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65566437 | ACTTTTTCAAGACTT[C/T]CTGTGACAAAACATT | 23398 |
| rs145865216 | snp | C/T | 4.94947e-05 | 0.00497443 | missense, intron-variant | PPWD1 | GRCh38.p7 | 5:65571985 | TTGACAAACTCCATA[C/T]ATCACCTCTTACTCA | 23398 |
| rs146125352 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPWD1 | GRCh38.p7 | 5:65570850 | GCTCATTAACCTTAA[C/T]TACCTCCTGAAGACC | 23398 |
| rs146649254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | PPWD1 | GRCh38.p7 | 5:65568471 | TAAATCCTAGAAGAC[C/T]TTTTATTTCTTGTAC | 23398 |
| rs146688769 | snp | C/T | 0 | 0 | intron-variant, utr-variant-5-prime | PPWD1 | GRCh38.p7 | 5:65568880 | GCATTGCTGTCACTC[C/T]CTTCTCAAATATTTT | 23398 |
| rs147222048 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65564670 | GCATATAAAGCCCTT[G/T]ATGATGTGATCTCTC | 23398 |
| rs147237486 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | PPWD1 | GRCh38.p7 | 5:65572578 | TCCTCAAAACTCATT[C/T]TAGGACCCCTTATCT | 23398 |
| rs147267922 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant, upstream-variant-2KB | PPWD1, CENPK | GRCh38.p7 | 5:65565170 | TATTTATTCATGTGA[G/T]TGATGAATGTTTCTC | 23398 |
| rs147425015 | snp | A/G | 0.000508768 | 0.0159413 | missense | PPWD1 | GRCh38.p7 | 5:65579575 | CAAGCTGACCCAACA[A/G]TAGTCTGTACATCAT | 23398 |
| rs147434634 | snp | A/G | 1.64844e-05 | 0.00287087 | upstream-variant-2KB, utr-variant-5-prime, missense | CENPK, PPWD1 | GRCh38.p7 | 5:65563368 | AGGCGCCGGGACCCG[A/G]AGGAACCGGAAAAAA | 23398 |
| rs147705132 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65561618 | CACACACACACACAC[A/G]CTTAAGAGTTGAACT | 23398 |
| rs147810009 | snp | A/C | 0.0182019 | 0.0936463 | intron-variant | PPWD1 | GRCh38.p7 | 5:65584590 | GGCCAGGTACAGTGG[A/C]TCAGGCCTGTAATCT | 23398 |
| rs147813053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65581345 | AAAAACAGCACTTTG[C/T]GGGGGCCCAAGCAGA | 23398 |
| rs148040392 | snp | C/T | 0.0279526 | 0.114869 | upstream-variant-2KB, intron-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65564414 | GCTCACCGCAACCTC[C/T]GTCTCCGGGGTTCAA | 23398 |
| rs148071179 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | PPWD1 | GRCh38.p7 | 5:65581989 | ATTTTACAAATCCAT[A/C]TATCAGCTAAGTCAT | 23398 |
| rs148076666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65587228 | TTGGGGTTTACCAAG[A/G]TTTTCCATTTGTCCT | 23398 |
| rs148122827 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPWD1 | GRCh38.p7 | 5:65578267 | ATCTTGGTTGCTTCC[A/G]AGTTTTGGCAGTTAT | 23398 |
| rs148562396 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65566595 | GTAGTTTATCAGACA[C/G]AAGCCTGAAACAGCT | 23398 |
| rs148592384 | snp | A/G | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65584321 | TCTTAGAAGTATTAC[A/G]TGGTAATGAACCGTA | 23398 |
| rs148617346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65573303 | ATTTTTTATTATTTA[C/T]TTATTTAATTAATTT | 23398 |
| rs148720992 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPWD1 | GRCh38.p7 | 5:65573275 | TAGTCATCCTGTCTT[A/G]CACAGTTTTTTTATT | 23398 |
| rs148827141 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPWD1 | GRCh38.p7 | 5:65574875 | ACAAGAAGTCAGTAG[C/T]AGAACTTAAGACAGA | 23398 |
| rs149176446 | snp | C/T | 5.82881e-05 | 0.00539821 | upstream-variant-2KB, missense, utr-variant-5-prime | CENPK, PPWD1 | GRCh38.p7 | 5:65563492 | TGGAGGCAACACTGG[C/T]CAAGAAGAGGAAAGG | 23398 |
| rs149293765 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65563608 | TGTGGAGTTTTGTGC[C/T]CTCAGAACAGAGGGC | 23398 |
| rs149362970 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | PPWD1 | GRCh38.p7 | 5:65578239 | CAGTTGATCCATTCA[C/T]GTACTGAAAGACATC | 23398 |
| rs149471709 | snp | A/G | 1.67632e-05 | 0.00289505 | synonymous-codon, intron-variant | PPWD1 | GRCh38.p7 | 5:65572256 | ATTTGTAACTGGAAA[A/G]CTCATGAGAGTCTTT | 23398 |
| rs149511641 | snp | C/T | 0.00380681 | 0.0434616 | synonymous-codon, intron-variant, utr-variant-5-prime | PPWD1 | GRCh38.p7 | 5:65569903 | GAGTATTGCAGTTAG[C/T]TCTGAGGGAGCATTG | 23398 |
| rs149648819 | snp | A/C | | | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65566782 | CTCCCTTCTTTCCTT[A/C]CTTACTTCCCTCCCT | 23398 |
| rs149787698 | snp | A/G | 0.0001156 | 0.00760176 | missense | PPWD1 | GRCh38.p7 | 5:65587289 | ACAGTATTTGGACGA[A/G]TGACTAAAGGAATGG | 23398 |
| rs149803979 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PPWD1 | GRCh38.p7 | 5:65565689 | GGCGCACACCTATAA[C/T]CTCAGCTATTCAGGA | 23398 |
| rs149886731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65580568 | GCCCAGGCTAGAGTG[C/T]AGTGACGTGACTTCA | 23398 |
| rs149940260 | snp | C/T | 0.00249721 | 0.0352472 | synonymous-codon | PPWD1 | GRCh38.p7 | 5:65585065 | CAGAAATGGTTATTA[C/T]AATGGGCATACATTT | 23398 |
| rs150307628 | snp | A/G | 0.000399281 | 0.0141238 | missense, intron-variant | PPWD1 | GRCh38.p7 | 5:65572173 | GCTTATCCAACCAGC[A/G]TATGTTTTTCACCAG | 23398 |
| rs150328237 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PPWD1 | GRCh38.p7 | 5:65569528 | TTTTTTAAAAAAAAA[C/T]CTATTATGCACAAGT | 23398 |
| rs150410430 | snp | C/G | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65582073 | AAAACTGGAGAATAG[C/G]ATGTTAAGGTGATAG | 23398 |
| rs150487053 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | CENPK, PPWD1 | GRCh38.p7 | 5:65562987 | AGAACGGGACTCAAA[A/G]CCCGGCTGGGAAGTC | 23398 |
| rs150499988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65584457 | AGGTTTTGGCCAAGA[A/G]TATGTCGCTGTAGCA | 23398 |
| rs150967524 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | PPWD1 | GRCh38.p7 | 5:65576501 | CTTGCCCCAGCCTCC[C/T]GAGTAGCTGGGATTA | 23398 |
| rs151288282 | snp | A/G | 0.000199213 | 0.00997832 | missense, intron-variant | PPWD1 | GRCh38.p7 | 5:65571868 | AGTGTGAGTGGATCT[A/G]TTGCCCAGGGGATGC | 23398 |
| rs151319862 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65562497 | CGACGAGGATTTTAT[C/T]AGGTTGGTGCAAAAG | 23398 |
| rs180679160 | snp | A/T | 0.0283406 | 0.115616 | intron-variant | PPWD1 | GRCh38.p7 | 5:65569091 | AAGGTAATATGTACA[A/T]AGTACCTGACATATA | 23398 |
| rs180689739 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65577460 | TTAAAATGCATGAAA[C/G]CACAGTAAGCCTTTT | 23398 |
| rs181153523 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65567891 | GAAGAAGAGGGTACA[G/T]TAGTTAAGATATGAG | 23398 |
| rs181161125 | snp | A/G | 0.00199481 | 0.0315187 | downstream-variant-500B | PPWD1 | GRCh38.p7 | 5:65587715 | CATGGTTTTCTTTCT[A/G]CTGTCAACCATGATC | 23398 |
| rs181209608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65578405 | GTTTAGTTTTGTAAC[A/G]GCCAAACTGCCTTTC | 23398 |
| rs181331984 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PPWD1 | GRCh38.p7 | 5:65574391 | TATTAACTTGCAGCT[C/T]TTCCAAGATCCCTTA | 23398 |
| rs181358729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65561791 | TACTTAAAGAAACTC[A/G]TACTATTAATTGGGA | 23398 |
| rs181370128 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPWD1 | GRCh38.p7 | 5:65583976 | AAATTACAACAAAAC[C/T]GTAAGGGCTTCAATT | 23398 |
| rs181381362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65562217 | CTGAAAGATGAGAAG[C/T]TGTAAACATGAAGGC | 23398 |
| rs181470869 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPWD1 | GRCh38.p7 | 5:65582780 | AAATGTTTGCCCAAG[A/G]AAATTTCTAACCAAA | 23398 |
| rs181630309 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPWD1 | GRCh38.p7 | 5:65573574 | CAGACGGGTTTCACC[A/G]TGTTAGCCAGGCTGG | 23398 |
| rs181881593 | snp | G/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65573867 | TTTTGAAAGAGTGAC[G/T]CTAGCCATCACTTGT | 23398 |
| rs182010152 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | PPWD1 | GRCh38.p7 | 5:65584508 | AATGACCTTTCCCAG[G/T]AACTTAACCTATACT | 23398 |
| rs182207445 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | PPWD1 | GRCh38.p7 | 5:65568379 | GAGTTAGTACATGCT[C/G]TTCATTTTAGAGATG | 23398 |
| rs182351522 | snp | C/T | 0.000612976 | 0.0174961 | intron-variant | PPWD1 | GRCh38.p7 | 5:65579654 | ACGGTAATGTTCCTT[C/T]CAGTTTGGTTTGACT | 23398 |
| rs182555483 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PPWD1 | GRCh38.p7 | 5:65575997 | AAACAGTCACTAGCC[A/G]CGTGTCTACTGAGCA | 23398 |
| rs182599955 | snp | A/C | 0.00043924 | 0.0148131 | intron-variant | PPWD1 | GRCh38.p7 | 5:65570042 | TAACTTATTGAAGTA[A/C]TTTGTAAATCAGACT | 23398 |
| rs182857335 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | PPWD1 | GRCh38.p7 | 5:65580926 | CATCAATAATTTATT[G/T]TTTTGGCCTCTGACG | 23398 |
| rs183061244 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65565235 | AATCACGCCTTTTTT[G/T]TTTCATTGCTTGGTG | 23398 |
| rs183157615 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PPWD1 | GRCh38.p7 | 5:65575401 | AAGAAAACCTAACAA[C/G]TAGGCTTTTTAACTG | 23398 |
| rs183180289 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPWD1 | GRCh38.p7 | 5:65565618 | ACCAGCCTGACCAAC[A/G]TGGTGAAACCCCGCC | 23398 |
| rs183185034 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65585822 | TGTTTCAATCAAGGT[C/G]GTGGTTGGGCAATGG | 23398 |
| rs183310659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65585219 | GGAACAGGAAAAATA[C/T]ACTATGGAAGCCAAA | 23398 |
| rs183326096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65578660 | GAAGGTCCTTGGGAC[A/G]TTTTTTAATTGGGTT | 23398 |
| rs183756037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65571451 | GGATTTATAAAATAC[A/G]CTATTACATGCTAAT | 23398 |
| rs183855945 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65574859 | TGATTAGCCTGAGGT[C/G]ACAAGAAGTCAGTAG | 23398 |
| rs183873581 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PPWD1 | GRCh38.p7 | 5:65572599 | CCCCTTATCTTCTCA[C/G]TCTTTATTCACTCCT | 23398 |
| rs183929267 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65570653 | TCTGGAGGCTGGAAA[G/T]TCCAAGATCAAGGTT | 23398 |
| rs183987083 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | CENPK, PPWD1 | GRCh38.p7 | 5:65562859 | AGAAAACATGTTTAG[C/T]GCATCTGAAAGGAAA | 23398 |
| rs184004451 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65567317 | CTGACTAAATAATGA[C/T]GCTATTCAGTGCTCT | 23398 |
| rs184451205 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65568157 | CAGCAAGTATAATGT[A/G]AATATTCTAAAATCT | 23398 |
| rs184458559 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | PPWD1 | GRCh38.p7 | 5:65587824 | GCTATAGTTGTTCTA[C/T]TTTATTGTTGTTAAT | 23398 |
| rs184495501 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65561288 | AAAGTCAAACATAAA[C/T]ATTTCTTTACTGACC | 23398 |
| rs184631155 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65582421 | GATCCATTTCAGATT[C/G]ATTTTTGTGAATCCT | 23398 |
| rs184778131 | snp | C/T | 1.67281e-05 | 0.00289202 | missense | PPWD1 | GRCh38.p7 | 5:65577068 | AATGTAGAGACAAAC[C/T]GGTAAGCTTTAATAT | 23398 |
| rs184933465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65581402 | CCTGCCTGGGCAACA[C/T]AGCAAGACCTCATCT | 23398 |
| rs185278807 | snp | A/T | 0.0283406 | 0.115616 | intron-variant | PPWD1 | GRCh38.p7 | 5:65569092 | AGGTAATATGTACAA[A/T]GTACCTGACATATAC | 23398 |
| rs185425052 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | PPWD1 | GRCh38.p7 | 5:65574141 | TCTAGTGGCGATCTT[G/T]ATTTGGTGGCACGTG | 23398 |
| rs185426437 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | PPWD1 | GRCh38.p7 | 5:65576533 | AGGCACACATCACCA[G/T]GCCCGGCTAAGTTTT | 23398 |
| rs185435195 | snp | C/G | 0.000620967 | 0.0176096 | intron-variant | PPWD1 | GRCh38.p7 | 5:65587217 | ATTTAAAGAAATTGG[C/G]GTTTACCAAGATTTT | 23398 |
| rs185566347 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65573611 | ACTCCTGGCCTCAAG[A/T]GATCTGCCTGCCTTG | 23398 |
| rs185577617 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65566431 | GGGTACACTTTTTCA[A/T]GACTTCCTGTGACAA | 23398 |
| rs185845457 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65562247 | CTAAATCGCTGTGGA[A/G]ATGCTTTCAAGCATA | 23398 |
| rs185853421 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPWD1 | GRCh38.p7 | 5:65584131 | ACTTAAAAGTTCTTA[C/T]TTATTAACATTTTGA | 23398 |
| rs185953918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65577526 | AGCTACAATCAGATA[C/T]TCTCACTGAATGTAA | 23398 |
| rs186058465 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | CENPK, PPWD1 | GRCh38.p7 | 5:65562980 | GCCGAGAAGAACGGG[A/G]CTCAAAGCCCGGCTG | 23398 |
| rs186092918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65578875 | AGTCCTTTATGAGCC[A/G]TTCTCCTAGTCTGTG | 23398 |
| rs186174495 | snp | C/T | 0.000636155 | 0.0178234 | intron-variant | PPWD1 | GRCh38.p7 | 5:65585122 | AAATTTCATGTCATA[C/T]AAGAAATACTGTATT | 23398 |
| rs186208591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65583396 | CGGTAGAAAATGGGA[A/G]ATTTTTATGCATATA | 23398 |
| rs186375139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65561873 | ACATTCATTTATTCA[A/G]CAAATATGTTAATGT | 23398 |
| rs186591972 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PPWD1 | GRCh38.p7 | 5:65571780 | GTAGTGGGATAGGGA[C/G]GGATGCTTGCTTGTT | 23398 |
| rs186699904 | snp | G/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65574996 | AAGGAGGTGGTAGTG[G/T]AGGAGGGTAGTTTCT | 23398 |
| rs186724655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65575461 | CCCTAACACACATAC[C/T]TCATTTTGATTTTTT | 23398 |
| rs187015822 | snp | C/G/T | 0.00318978 | 0.0398085 | intron-variant | PPWD1 | GRCh38.p7 | 5:65565342 | GAATATTTTTGCAAG[C/G/T]TCTTTTTTAATTAAA | 23398 |
| rs187073214 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65578463 | CACCAGCAATGAATG[A/T]GTGTTCCTGTCACTC | 23398 |
| rs187239193 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | PPWD1 | GRCh38.p7 | 5:65568688 | GAAGTAGGTGGATTA[C/T]TTTACACTTTTTTAG | 23398 |
| rs187467249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65566213 | CGATGTTGAAGAGAT[A/G]GAGCTGTACTTTTAT | 23398 |
| rs187476839 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPWD1 | GRCh38.p7 | 5:65587010 | GAAGATCTTCCAGTT[C/T]CCTTTGGTCTGAAAG | 23398 |
| rs187566030 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PPWD1 | GRCh38.p7 | 5:65580383 | TTCATTCATTTGCTA[A/C]ACGAACCATACTGAA | 23398 |
| rs187595233 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPWD1 | GRCh38.p7 | 5:65570166 | AGCCTTATAATGTTT[A/G]GAAGCATCTGCTATG | 23398 |
| rs187656577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65566746 | CTTCTTCTCTCCCTC[C/T]CTCCCTTCGTCTTTC | 23398 |
| rs187803227 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65585307 | TTAGAAACACTGAAG[A/C]AATATTTTGTCAGCA | 23398 |
| rs187920768 | snp | C/T | 3.30278e-05 | 0.0040636 | missense | PPWD1 | GRCh38.p7 | 5:65587290 | CAGTATTTGGACGAG[C/T]GACTAAAGGAATGGA | 23398 |
| rs188074375 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPWD1 | GRCh38.p7 | 5:65576227 | ACTTTAAAATTACCT[A/G]TGTGGCTTGTGTTAT | 23398 |
| rs188329302 | snp | C/G | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65577319 | TTCAAGTTGTTGTGT[C/G]TTTTTTTTAACAAGT | 23398 |
| rs188720458 | snp | A/G | 0.000214764 | 0.0103603 | missense, utr-variant-5-prime, intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65567562 | CCCCAGTGCATCCAT[A/G]TATGAGCGCAGTTAC | 23398 |
| rs188725699 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | PPWD1 | GRCh38.p7 | 5:65581007 | CTTCACTGTTAAATC[C/G]AGAAAGTTAGGAAAT | 23398 |
| rs188726776 | snp | A/T | 0.000798403 | 0.0199641 | downstream-variant-500B | PPWD1 | GRCh38.p7 | 5:65587619 | ACTAAACTCAGGCAA[A/T]TAGCACTCATTATAG | 23398 |
| rs188845284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65568204 | AAAACACTTCTGGTC[C/T]GATACATTTTGGATA | 23398 |
| rs188880637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65570726 | CTCCCTATGTTCTCC[C/T]ATGGTTGGAGGAAGA | 23398 |
| rs188986133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65562108 | AAACCAACCCGGAAG[A/G]AATTAGTCCATAATA | 23398 |
| rs189075087 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65582471 | TCCTGCTCATAGTAG[G/T]AATAACAACTGTTAA | 23398 |
| rs189373120 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime, missense | CENPK, PPWD1 | GRCh38.p7 | 5:65561481 | TTGAGGATGCAAGAT[A/G]TAAGCTGTATGTAAC | 23398 |
| rs189646881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65581987 | TGATTTTACAAATCC[A/G]TATATCAGCTAAGTC | 23398 |
| rs189720769 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PPWD1 | GRCh38.p7 | 5:65579296 | GGTAGAGAAACACTT[C/T]TAAAAATCTTTCACT | 23398 |
| rs189742545 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPWD1 | GRCh38.p7 | 5:65574237 | TTTGCCAGCCAAATT[A/G]TCCTTATGACAAATT | 23398 |
| rs189903690 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PPWD1 | GRCh38.p7 | 5:65576578 | AGACGGGGTTTCACC[A/G]TGTTGGCCAGGCTGT | 23398 |
| rs190047136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65573416 | TCCTGTCTCAGCTTC[C/T]CAAGTAGCTGGGACT | 23398 |
| rs190241424 | snp | G/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65585639 | GGAATTAGCGAAAAG[G/T]CTTTCCAGGAAATCC | 23398 |
| rs190380222 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PPWD1 | GRCh38.p7 | 5:65578621 | CTATTTACCATTTGT[A/G]TATCTCTTTGATGAA | 23398 |
| rs190381486 | snp | C/T | 0.00635483 | 0.0560092 | intron-variant | PPWD1 | GRCh38.p7 | 5:65570030 | GTATATATATTTTAA[C/T]TTATTGAAGTAATTT | 23398 |
| rs190647924 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPWD1 | GRCh38.p7 | 5:65565476 | AGTAGGTGTGAAAAT[C/T]TTTCCTCTTAATCAG | 23398 |
| rs190649763 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65585188 | CTTCTCTCACACTTA[A/C]TCAGTTTAGTGGAAA | 23398 |
| rs190816397 | snp | A/T | 0.0283406 | 0.115616 | intron-variant | PPWD1 | GRCh38.p7 | 5:65569090 | TAAGGTAATATGTAC[A/T]AAGTACCTGACATAT | 23398 |
| rs190821720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65573730 | TTAGAGCATTTGATA[C/T]GGTCATATTATTTGA | 23398 |
| rs190919509 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65563090 | AACCTCCCCGGCCCA[G/T]GTCTTACCATCACAG | 23398 |
| rs191037795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65562281 | ACATAAGAGTAGGAG[A/G]CAAGAACGAACAAGG | 23398 |
| rs191048078 | snp | C/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65584505 | GAAAATGACCTTTCC[C/T]AGGAACTTAACCTAT | 23398 |
| rs191141287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65575767 | TTTCCAAACTATAAA[A/G]GACACTTATAGAAAT | 23398 |
| rs191598727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65574758 | GTGAGCCACCGCGCC[C/T]GGCCGGCACAAATCT | 23398 |
| rs191705379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65570474 | TTTGTTTTAAGCATG[C/T]CTTTTTTAAGATAAC | 23398 |
| rs191791729 | snp | G/T | | | missense, intron-variant | PPWD1 | GRCh38.p7 | 5:65572171 | AGGCTTATCCAACCA[G/T]CGTATGTTTTTCACC | 23398 |
| rs191998353 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PPWD1 | GRCh38.p7 | 5:65581239 | TATGAAGGAAAAAAA[C/T]TAATCGTTTTACCTT | 23398 |
| rs192430241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65575394 | TAGAGACAAGAAAAC[C/T]TAACAACTAGGCTTT | 23398 |
| rs192498753 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PPWD1 | GRCh38.p7 | 5:65582128 | GAATCTATCCAAGCA[C/G]ATCAAGGAATGACAT | 23398 |
| rs192566316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65567256 | ACTCATTTCTTAAGT[C/T]CTGGGGACAGTTAGC | 23398 |
| rs192589894 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65576628 | GATCCACCTGCCTTG[G/T]CCTCCCAAAATGCTG | 23398 |
| rs192595555 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65587177 | AAACTTAAATTCTCT[G/T]TAATTTGCTCAACCA | 23398 |
| rs192697663 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPWD1 | GRCh38.p7 | 5:65576531 | ACAGGCACACATCAC[C/T]ATGCCCGGCTAAGTT | 23398 |
| rs192969019 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | PPWD1 | GRCh38.p7 | 5:65580789 | AAAGTGCTGGAATTA[C/G]AGGCGTGAGCCACCG | 23398 |
| rs193096520 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PPWD1 | GRCh38.p7 | 5:65570916 | TGTGGGCTGAATTAT[G/T]CCCACAATTCAAATA | 23398 |
| rs193129807 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65566348 | CTCATCTTCATTTCT[C/G]TGAATGATTATTAAG | 23398 |
| rs199517260 | in-del | -/T | 0.0418186 | 0.138422 | intron-variant | PPWD1 | GRCh38.p7 | 5:65573498 | TTTATTAGAGATGGG[-/T]TTTTTTTAGTACAGA | 23398 |
| rs199533597 | in-del | -/A | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65585864 | CCAAATTTAAGTGTT[-/A]AGGGTTTAATCAAAT | 23398 |
| rs199538660 | in-del | -/CTCTC | 0.030665 | 0.119967 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65566737 | TTTCTCTTCCTTCTT[-/CTCTC]CCTCCCTCCCTTCGT | 23398 |
| rs199602684 | snp | A/C | 1.6863e-05 | 0.00290365 | missense, utr-variant-5-prime, intron-variant | PPWD1 | GRCh38.p7 | 5:65569634 | TTCATATATGCAGAA[A/C]AGATTTTATTATTAC | 23398 |
| rs199650174 | snp | G/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65571769 | AGACATTTTTGGTAG[G/T]GGGATAGGGAGGGAT | 23398 |
| rs199760035 | snp | C/T | 0.00076631 | 0.0195593 | upstream-variant-2KB, utr-variant-5-prime | CENPK, PPWD1 | GRCh38.p7 | 5:65563289 | AGTTTTGTGTCGCGC[C/T]TTTTCTGACGATGCG | 23398 |
| rs199761656 | snp | A/C | | | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65566812 | TCATTCTCTCCATCC[A/C]TTTCTTTCTTTTTTT | 23398 |
| rs199790239 | snp | C/G/T | 0.000115489 | 0.00759817 | missense, intron-variant | PPWD1 | GRCh38.p7 | 5:65571972 | CCACTTCATATTTTT[C/G/T]ACAAACTCCATACAT | 23398 |
| rs199914013 | in-del | -/A | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65573471 | CTAATATATATATAT[-/A]TATATTTTTTTTTTA | 23398 |
| rs199936033 | snp | A/G | 1.64819e-05 | 0.00287066 | missense | PPWD1 | GRCh38.p7 | 5:65576952 | GAATGGCTGTAGAAC[A/G]TGAGTTGGAGAAGGT | 23398 |
| rs199948689 | snp | G/T | 1.65652e-05 | 0.0028779 | upstream-variant-2KB, utr-variant-5-prime, missense | CENPK, PPWD1 | GRCh38.p7 | 5:65563335 | GAAAGTGGTAGCGAT[G/T]TTCAGCAGAGACGTA | 23398 |
| rs199952911 | snp | A/G | | | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65566496 | AACCTCACTCCAGGG[A/G]AAAGTGAGAAAGGTC | 23398 |
| rs200034433 | in-del | -/TTC | | | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65566818 | TCTCCATCCCTTTCT[-/TTC]TTTTTTTTTTTTTGC | 23398 |
| rs200088481 | in-del | -/TATACACACATATATGTGTATAT | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65578743 | ATATATACATATATA[-/TATACACACATATATGTGTATAT]ATATATACATATATA | 23398 |
| rs200107819 | snp | A/T | 0.00199792 | 0.0315431 | stop-gained | PPWD1 | GRCh38.p7 | 5:65583149 | CAAGCTGAAGGACCT[A/T]AACGAGTTTCGGACA | 23398 |
| rs200281206 | snp | A/G | 7.07026e-05 | 0.00594528 | intron-variant | PPWD1 | GRCh38.p7 | 5:65585124 | ATTTCATGTCATATA[A/G]GAAATACTGTATTAT | 23398 |
| rs200283546 | snp | A/G | 0.00115616 | 0.0240155 | intron-variant | PPWD1 | GRCh38.p7 | 5:65569590 | ACTAAGTGATTCATA[A/G]ATCTGTCTTAGAAAT | 23398 |
| rs200313500 | in-del | -/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65573471 | TAATATATATATATA[-/T]TATATTTTTTTTTTA | 23398 |
| rs200365809 | snp | G/T | 8.49755e-05 | 0.00651771 | splice-donor-variant, intron-variant | PPWD1 | GRCh38.p7 | 5:65569999 | CATGCTGAAACTTGG[G/T]TGAGTCTTTTTAAAA | 23398 |
| rs200375992 | snp | C/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65576124 | TCCAGAATATCATCT[C/T]AACAATATAAAAAAT | 23398 |
| rs200528307 | in-del | -/A | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65573475 | TATATATATATATAT[-/A]TTTTTTTTTTATTAG | 23398 |
| rs200678289 | in-del | -/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65569510 | CTGCTTAAAGAAGGG[-/T]TTTTTTTTAAAAAAA | 23398 |
| rs200690383 | snp | C/T | | | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65566814 | ATTCTCTCCATCCCT[C/T]TCTTTCTTTTTTTTT | 23398 |
| rs200702127 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | PPWD1 | GRCh38.p7 | 5:65578780 | TATATATACATATAT[A/G]TGTGTATATATATAT | 23398 |
| rs200739537 | snp | A/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65573481 | TATATATATATTTTT[A/T]TTTTATTAGAGATGG | 23398 |
| rs200744611 | snp | C/T | 1.65173e-05 | 0.00287374 | missense | PPWD1 | GRCh38.p7 | 5:65577036 | TGTATGGAACAATGC[C/T]GGGCATTAAAGTTAT | 23398 |
| rs200756355 | snp | A/G | | | stop-gained | PPWD1 | GRCh38.p7 | 5:65587258 | TCCAACACAGCCTTG[A/G]CTTGATAATAAGCAT | 23398 |
| rs200778132 | snp | A/G | 4.9643e-05 | 0.00498187 | missense | PPWD1 | GRCh38.p7 | 5:65579518 | CGTGCTGCAACTACT[A/G]TAGAAATGAAAGCTT | 23398 |
| rs200785833 | snp | A/T | | | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65561780 | GGATAATACTATACT[A/T]AAAGAAACTCGTACT | 23398 |
| rs200863310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65572310 | AATTTAAATTTAACC[A/G]TACTTTACTTTTCTA | 23398 |
| rs200884267 | snp | A/G | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65578581 | TTTCCCTGGCAACAT[A/G]TGAGGTGGAGTATCT | 23398 |
| rs201113007 | snp | A/G | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65584878 | GAGATTAGAGATTAT[A/G]AAAAAAAAAAACAAC | 23398 |
| rs201137891 | snp | G/T | 0.176219 | 0.238865 | downstream-variant-500B | PPWD1 | GRCh38.p7 | 5:65587887 | TATCATAGATATATA[G/T]ATATGAAAACACAAT | 23398 |
| rs201155013 | snp | A/G | 6.60219e-05 | 0.00574513 | missense, intron-variant | PPWD1 | GRCh38.p7 | 5:65571948 | TATGATGGCCGAGGA[A/G]ATAACCAGCCACTTC | 23398 |
| rs201191647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65583223 | TTTTCCTGTTGAGTA[C/T]GTATAACAACTGTTT | 23398 |
| rs201295161 | in-del | -/A | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65573476 | TATATATATATATAT[-/A]TTTTTTTTTATTAGA | 23398 |
| rs201333011 | snp | C/T | | | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65566815 | TTCTCTCCATCCCTT[C/T]CTTTCTTTTTTTTTT | 23398 |
| rs201414471 | snp | A/C | 0.00201776 | 0.0316987 | missense, utr-variant-5-prime, intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65567519 | TTTCTTCAGTCTTAG[A/C]GTTTGAAAGAGTCTA | 23398 |
| rs201417257 | in-del | -/C | | | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65566820 | TCCATCCCTTTCTTT[-/C]TTTTTTTTTTTTTGC | 23398 |
| rs201428744 | snp | C/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65578771 | ATGTGTATATATATA[C/T]ACATATATATGTGTA | 23398 |
| rs201451251 | in-del | -/TTTCT | | | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65566817 | CTCTCCATCCCTTTC[-/TTTCT]TTTTTTTTTTTTGCT | 23398 |
| rs201469847 | in-del | -/TACT | 0.0134861 | 0.0810011 | upstream-variant-2KB, intron-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65563649 | CTTCTGGCTACTCCA[-/TACT]TGCATGTCTTAACGA | 23398 |
| rs201500460 | snp | G/T | 8.43135e-05 | 0.00649227 | missense, intron-variant | PPWD1 | GRCh38.p7 | 5:65572261 | TAACTGGAAAACTCA[G/T]GAGAGTCTTTGATGA | 23398 |
| rs201626408 | snp | C/G | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65577371 | ATTTAAATTAGCCTG[C/G]TTCATGTTAAATGTT | 23398 |
| rs201672695 | snp | A/G | 0.000216744 | 0.0104079 | missense, intron-variant, utr-variant-5-prime | PPWD1 | GRCh38.p7 | 5:65569991 | ATGATCAACATGCTG[A/G]AACTTGGGTGAGTCT | 23398 |
| rs201676226 | snp | A/G | 0.00010721 | 0.00732075 | synonymous-codon | PPWD1 | GRCh38.p7 | 5:65579598 | TACATCATTCAAAAA[A/G]AATAGATTTTATATG | 23398 |
| rs201680349 | in-del | -/G | 0.0490535 | 0.14873 | intron-variant | PPWD1 | GRCh38.p7 | 5:65576758 | AAGTACAAACAGTTA[-/G]TGGCTCTTAATATGT | 23398 |
| rs201688187 | snp | A/G | 0.00199792 | 0.0315431 | stop-gained | PPWD1 | GRCh38.p7 | 5:65586057 | GAGGAGAAAGCATAT[A/G]GGGAGGAGAATTTGA | 23398 |
| rs201716299 | snp | A/G | | | missense | PPWD1 | GRCh38.p7 | 5:65583187 | TATCCACACCAGCAT[A/G]GGAGACATTCACACC | 23398 |
| rs201749037 | in-del | -/TCTC | | | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65566736 | CTTTCTCTTCCTTCT[-/TCTC]TCCCTCCCTCCCTTC | 23398 |
| rs201768677 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65578441 | GGCTATACTCTTTTT[A/G/T]CATTCCCACCAGCAA | 23398 |
| rs201855907 | in-del | -/AG | | | downstream-variant-500B | PPWD1 | GRCh38.p7 | 5:65587881 | AACTTTATCATAGAT[-/AG]ATATATATATGAAAA | 23398 |
| rs201905835 | snp | A/G | 0.00012266 | 0.00783037 | utr-variant-3-prime | PPWD1 | GRCh38.p7 | 5:65587398 | TTACTGTCAAGTAAA[A/G]TAAGATTTGTTTTAA | 23398 |
| rs201915198 | snp | A/G/T | 0.000217639 | 0.0104295 | synonymous-codon | PPWD1 | GRCh38.p7 | 5:65583064 | AGAACCAGAAGATAC[A/G/T]AAAAGTGCAGATTCT | 23398 |
| rs201929411 | snp | A/G | 0.00150166 | 0.0273601 | missense | PPWD1 | GRCh38.p7 | 5:65587317 | TGGAAGTTGTACAGA[A/G]GATCTCCAACGTCAA | 23398 |
| rs202237644 | snp | C/T | 3.40501e-05 | 0.004126 | upstream-variant-2KB, intron-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65563546 | CGAATTGGAGTGCTG[C/T]GTCCGCTGAGTAGGA | 23398 |
| rs367559714 | snp | A/G | 0.000153988 | 0.00877328 | missense | PPWD1 | GRCh38.p7 | 5:65586036 | ATCCAACAGGTACTG[A/G]TATGGGAGGAGAAAG | 23398 |
| rs367659519 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65574865 | GCCTGAGGTGACAAG[A/T]AGTCAGTAGTAGAAC | 23398 |
| rs367664212 | in-del | -/AAAAGGGG | | | upstream-variant-2KB, intron-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65564153 | AATAAAAGGGGTGGG[-/AAAAGGGG]TAGATTAAGTTTTCT | 23398 |
| rs367677973 | in-del | -/G | | | upstream-variant-2KB, intron-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65564062 | AAACCCGAAGTCTGG[-/G]TTTTGAAATCACGCT | 23398 |
| rs367716785 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65567035 | TCAAACACAGTGTCA[A/G]TAACTTGAAAGAGAA | 23398 |
| rs367745278 | snp | A/G | 3.43171e-05 | 0.00414215 | upstream-variant-2KB, utr-variant-5-prime | CENPK, PPWD1 | GRCh38.p7 | 5:65563302 | GCCTTTTCTGACGAT[A/G]CGAACAACATGGCGG | 23398 |
| rs368009355 | snp | A/G | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65579277 | AAATTGATACCTTTT[A/G]GGGGGTAGAGAAACA | 23398 |
| rs368031733 | snp | C/T | | | downstream-variant-500B | PPWD1 | GRCh38.p7 | 5:65587591 | AATCCTGGGAGGTGA[C/T]AAATTGAAATGGACT | 23398 |
| rs368183450 | snp | A/G | 3.52324e-05 | 0.00419702 | intron-variant | PPWD1 | GRCh38.p7 | 5:65577114 | AAAATGTGTTTGTGG[A/G]GGACCATTTCCTCCA | 23398 |
| rs368185365 | snp | A/C | 1.64985e-05 | 0.0028721 | missense, intron-variant | PPWD1 | GRCh38.p7 | 5:65572060 | AATCTGGGATGATTG[A/C]ATACTGGACTGGGCC | 23398 |
| rs368301551 | snp | A/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65573480 | ATATATATATATTTT[A/T]TTTTTATTAGAGATG | 23398 |
| rs368361977 | snp | A/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65584877 | TGAGATTAGAGATTA[A/T]GAAAAAAAAAAACAA | 23398 |
| rs368362886 | in-del | -/TCTCC | | | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65566738 | TTCTCTTCCTTCTTC[-/TCTCC]CTCCCTCCCTTCGTC | 23398 |
| rs368395764 | snp | A/T | 8.48976e-05 | 0.00651472 | intron-variant | PPWD1 | GRCh38.p7 | 5:65585002 | TCATATTTGTAACAT[A/T]TGTCTTAATAGGTGC | 23398 |
| rs368584720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65562275 | ATAAAAACATAAGAG[C/T]AGGAGGCAAGAACGA | 23398 |
| rs368660147 | snp | A/G | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65570349 | TAGAATTGAGTTCCT[A/G]TAAGATTTATTCACA | 23398 |
| rs368682011 | snp | C/G/T | 4.962e-05 | 0.00498072 | missense, synonymous-codon, intron-variant | PPWD1 | GRCh38.p7 | 5:65572172 | GGCTTATCCAACCAG[C/G/T]GTATGTTTTTCACCA | 23398 |
| rs368802870 | in-del | -/A/AA/AAA | 0.655358 | 0.112335 | intron-variant | PPWD1 | GRCh38.p7 | 5:65584878 | AGATTAGAGATTATG[-/A/AA/AAA]AAAAAAAAAAACAAC | 23398 |
| rs368870571 | snp | C/T | 8.29814e-05 | 0.00644079 | synonymous-codon | PPWD1 | GRCh38.p7 | 5:65579544 | AGCTTCTGAAAATCC[C/T]GTTCTTCAGAATATT | 23398 |
| rs369046878 | snp | A/G | 0.000140932 | 0.00839322 | upstream-variant-2KB, utr-variant-5-prime | CENPK, PPWD1 | GRCh38.p7 | 5:65563267 | GCTGCTTTGGGATTG[A/G]TAGCTGAGTTTTGTG | 23398 |
| rs369077366 | in-del | -/TTTTT | | | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65568301 | CTAAGGCTTTTTCTT[-/TTTTT]ATCTATCAAGTTAAG | 23398 |
| rs369143060 | in-del | -/AG | | | downstream-variant-500B | PPWD1 | GRCh38.p7 | 5:65587883 | CTTTATCATAGATAT[-/AG]ATATATATGAAAACA | 23398 |
| rs369223260 | snp | A/G | | | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65568125 | CATTTGAGATTTTCT[A/G]ATTAGGGATGTTCAA | 23398 |
| rs369233224 | snp | A/G | | | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65568080 | AGTTTTTGAGTGCTG[A/G]ACATGATACTCAAAA | 23398 |
| rs369274229 | snp | C/G | 0.000185914 | 0.00963963 | intron-variant | PPWD1 | GRCh38.p7 | 5:65579631 | ATGTGTAAGTACTAG[C/G]AGATTAGACGGTAAT | 23398 |
| rs369280927 | snp | A/C | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65565626 | GACCAACATGGTGAA[A/C]CCCCGCCAGTCTCTA | 23398 |
| rs369322532 | snp | A/G | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65576425 | TCTGTCCCCCAGGCC[A/G]GAGTGCAGTGGCGCA | 23398 |
| rs369388140 | snp | A/G | 4.80723e-05 | 0.00490243 | upstream-variant-2KB, intron-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65563519 | AAGGTAGCTGCAGAC[A/G]TAGTACCGGGACGAA | 23398 |
| rs369459984 | snp | A/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65573486 | ATATATTTTTTTTTT[A/T]TTAGAGATGGGTTTT | 23398 |
| rs369646530 | snp | A/C | 1.77294e-05 | 0.00297731 | intron-variant | PPWD1 | GRCh38.p7 | 5:65583029 | TCACTTTTTACTTTC[A/C]TCCTTGAGTTTACCA | 23398 |
| rs369664589 | snp | C/T | 5.07215e-05 | 0.00503569 | missense | PPWD1 | GRCh38.p7 | 5:65586168 | CCCAGTTTTTCATAA[C/T]GGTAGTACCAACGGT | 23398 |
| rs369867201 | snp | A/C | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65582691 | AATGAACTGAGCAAC[A/C]AACAGGTGGCATGTT | 23398 |
| rs369876217 | snp | A/G | 1.79367e-05 | 0.00299467 | intron-variant | PPWD1 | GRCh38.p7 | 5:65571793 | GAGGGATGCTTGCTT[A/G]TTGTGCTGACCTTTT | 23398 |
| rs370159993 | snp | C/T | | | intron-variant, utr-variant-5-prime | PPWD1 | GRCh38.p7 | 5:65568904 | ATATTTTTGTTTTGT[C/T]TTTTTAACCCAAGAC | 23398 |
| rs370241841 | snp | C/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65580078 | TCCTGTGGAATTTTT[C/T]TTTTCTCTTCTGGAG | 23398 |
| rs370309232 | snp | A/T | 0.000153988 | 0.00877328 | upstream-variant-2KB, intron-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65563555 | GTGCTGCGTCCGCTG[A/T]GTAGGAGGGTTCAAG | 23398 |
| rs370392254 | snp | C/T | 0.0566069 | 0.158427 | intron-variant | PPWD1 | GRCh38.p7 | 5:65578799 | GTATATATATATACA[C/T]ATATATGTGTATATA | 23398 |
| rs370514053 | snp | C/G | 3.34208e-05 | 0.0040877 | synonymous-codon | PPWD1 | GRCh38.p7 | 5:65583202 | GGGAGACATTCACAC[C/G]AAACTTTTTCCTGTT | 23398 |
| rs370540220 | snp | A/C/G | | | upstream-variant-2KB, intron-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65564292 | TCCCTTAAAAAACTT[A/C/G]AATGATTTGTCATTA | 23398 |
| rs370637902 | snp | A/C/T | 0.000122757 | 0.00783358 | intron-variant | PPWD1 | GRCh38.p7 | 5:65569616 | GAAATTAACTTTTAA[A/C/T]ATTTCATATATGCAG | 23398 |
| rs370712428 | snp | A/G | 2.43703e-05 | 0.00349064 | intron-variant | PPWD1 | GRCh38.p7 | 5:65579657 | GTAATGTTCCTTCCA[A/G]TTTGGTTTGACTTTT | 23398 |
| rs370731677 | snp | A/G | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65582861 | TTTTCATATTAGACA[A/G]TGTAAAAATAATTTA | 23398 |
| rs370898290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65569205 | CCAAAATACCTTGTA[C/T]AGGATATAAAAAAAA | 23398 |
| rs370920192 | in-del | -/G | | | upstream-variant-2KB, utr-variant-5-prime, frameshift-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65563420 | GGCAGTAGCAGTGGC[-/G]GGTGTCCCAGGAGAA | 23398 |
| rs371148868 | in-del | -/TTT | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65573476 | ATATATATATATATA[-/TTT]TTTTTTTATTAGAGA | 23398 |
| rs371241824 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPWD1 | GRCh38.p7 | 5:65585490 | AACCTGTAATATACC[A/G]GAGGAGGAGAGAGAA | 23398 |
| rs371309223 | snp | A/G | 4.94466e-05 | 0.00497201 | upstream-variant-2KB, utr-variant-5-prime, synonymous-codon | CENPK, PPWD1 | GRCh38.p7 | 5:65563376 | GGACCCGGAGGAACC[A/G]GAAAAAACAGAACTC | 23398 |
| rs371475524 | in-del | -/TAATT | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65580917 | TTGTGTGAACATCAA[-/TAATT]TATTTTTTTGGCCTC | 23398 |
| rs371494766 | snp | C/T | | | downstream-variant-500B | PPWD1 | GRCh38.p7 | 5:65587629 | GGCAAATAGCACTCA[C/T]TATAGGTAATTTCTA | 23398 |
| rs371507795 | snp | A/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65576116 | TTATCTCAATTTTTT[A/T]TATTGTTGAGATGAT | 23398 |
| rs371508328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65566929 | TTTTCCAGGTTTTGC[C/T]GTTGGAAAAAATTTG | 23398 |
| rs371623213 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65565134 | TTTTATTTATGGCAC[C/T]TGCCGCAGTTTCTAA | 23398 |
| rs371636721 | snp | A/C | 1.65119e-05 | 0.00287327 | missense, intron-variant | PPWD1 | GRCh38.p7 | 5:65572089 | CCTCCTCATGAATAT[A/C]AATTCCCCAAAAATG | 23398 |
| rs371711171 | snp | C/G | 2.31131e-05 | 0.00339941 | intron-variant | PPWD1 | GRCh38.p7 | 5:65572331 | TACTTTTCTAAAAAT[C/G]CTTTATTTTATGCCT | 23398 |
| rs371819967 | snp | A/C | 0.000415564 | 0.0144086 | intron-variant | PPWD1 | GRCh38.p7 | 5:65585135 | TATAAGAAATACTGT[A/C]TTATTACATAGCAAG | 23398 |
| rs372057466 | snp | C/T | 0.000153988 | 0.00877328 | upstream-variant-2KB, utr-variant-5-prime, stop-gained | CENPK, PPWD1 | GRCh38.p7 | 5:65563428 | GCAGTGGCGGTGTCC[C/T]AGGAGAACGATGAGG | 23398 |
| rs372108203 | snp | C/T | 1.86062e-05 | 0.00305004 | intron-variant | PPWD1 | GRCh38.p7 | 5:65579379 | TTGTCATAATTGGAA[C/T]TAACTTCGGTGATTC | 23398 |
| rs372181312 | snp | C/G | | | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65566946 | TTGGAAAAAATTTGA[C/G]ATACATTCAACTGGA | 23398 |
| rs372237115 | snp | C/G | | | missense | PPWD1 | GRCh38.p7 | 5:65587323 | TTGTACAGAGGATCT[C/G]CAACGTCAAAGTCAA | 23398 |
| rs372326593 | snp | C/T | 0.000316453 | 0.0125748 | intron-variant | PPWD1 | GRCh38.p7 | 5:65579386 | AATTGGAATTAACTT[C/T]GGTGATTCTGTTGTA | 23398 |
| rs372339150 | snp | C/T | 5.03808e-05 | 0.00501875 | missense | PPWD1 | GRCh38.p7 | 5:65585084 | GGGCATACATTTCAC[C/T]GTATAATTAAGGTAA | 23398 |
| rs372343876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65583823 | TGGGCATGGTGGCAC[A/G]CACCTGTATTCCTGG | 23398 |
| rs372468214 | snp | A/C | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65575583 | GTCTGGCTTATTTTC[A/C]TCTGCAATGGAGAGC | 23398 |
| rs372562429 | snp | C/T | 0.000878007 | 0.020934 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65567635 | GTCTATCACATCTTT[C/T]TTACTTTGTTCTGAG | 23398 |
| rs372573044 | snp | A/T | 5.06744e-05 | 0.00503335 | intron-variant | PPWD1 | GRCh38.p7 | 5:65577077 | ACAAACCGGTAAGCT[A/T]TAATATGAGGTATGT | 23398 |
| rs372592635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65570560 | AAAGTTTTGGGACTC[A/G]CCTTAGTCTGCTTGG | 23398 |
| rs372594535 | snp | A/G | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65578784 | TATACATATATATGT[A/G]TATATATATATACAT | 23398 |
| rs372619638 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65580192 | TTGTTCATCCAAGCA[C/G]GAAAATCAAAAGTAT | 23398 |
| rs372665206 | snp | C/T | | | utr-variant-3-prime | PPWD1 | GRCh38.p7 | 5:65587511 | TTCAAAGATACAGTA[C/T]TTTTGTATTTTTTAT | 23398 |
| rs372699520 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PPWD1 | GRCh38.p7 | 5:65574877 | AAGAAGTCAGTAGTA[A/G]AACTTAAGACAGAAG | 23398 |
| rs372704895 | in-del | -/TA | 0.359007 | 0.225696 | intron-variant | PPWD1 | GRCh38.p7 | 5:65578784 | ATACATATATATGTG[-/TA]TATATATATATACAT | 23398 |
| rs372733806 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65566596 | TAGTTTATCAGACAC[A/C]AGCCTGAAACAGCTC | 23398 |
| rs372882397 | in-del | -/TTTTT | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65573476 | ATATATATATATATA[-/TTTTT]TTTTTATTAGAGATG | 23398 |
| rs372978168 | snp | A/C | | | intron-variant, utr-variant-5-prime | PPWD1 | GRCh38.p7 | 5:65568963 | TTTGTGGTGTGGTAG[A/C]TTGAAAGCCACTCTA | 23398 |
| rs373003960 | snp | A/G | | | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65568190 | GAAATTGAAACTCCA[A/G]AACACTTCTGGTCCG | 23398 |
| rs373069024 | snp | A/G | 1.88852e-05 | 0.00307282 | intron-variant | PPWD1 | GRCh38.p7 | 5:65586227 | AGATTGATAGGTTAT[A/G]ATGTAAGAGAGTGAA | 23398 |
| rs373144568 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | PPWD1 | GRCh38.p7 | 5:65578957 | GGAGTCTTGTTCTGT[C/T]ACCCAGGCTGGAGAG | 23398 |
| rs373149806 | snp | A/C | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65580833 | AGCCCTTTTTAACAT[A/C]AAGTCTGAGTTAGAT | 23398 |
| rs373249979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65585441 | ATATGATTTTTCAAT[C/T]ATAGAGGAGCCACAG | 23398 |
| rs373286489 | snp | C/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65581191 | AGAATTTCATTTACA[C/T]CTTTCAAAATTATTA | 23398 |
| rs373288361 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65584686 | ATATAGTGAGACCTT[G/T]TCTCTTAAGAAAAAA | 23398 |
| rs373447649 | snp | C/T | 3.56094e-05 | 0.00421941 | intron-variant | PPWD1 | GRCh38.p7 | 5:65571803 | TGCTTGTTGTGCTGA[C/T]CTTTTTTTTTCCCTC | 23398 |
| rs373486443 | snp | C/T | 1.71953e-05 | 0.00293212 | stop-gained | PPWD1 | GRCh38.p7 | 5:65583047 | CTTGAGTTTACCAAA[C/T]GAGAACCAGAAGATA | 23398 |
| rs373488081 | snp | A/C | 3.31439e-05 | 0.00407073 | missense, intron-variant, utr-variant-5-prime | PPWD1 | GRCh38.p7 | 5:65569682 | ATGTCAAGTTCTGGA[A/C]AAAAATAGAAGAGGG | 23398 |
| rs373706734 | snp | A/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65577676 | AGACATGGAATTTTA[A/T]TAAGAATAGGTTAAA | 23398 |
| rs373766919 | snp | A/G | 6.46838e-05 | 0.00568662 | intron-variant | PPWD1 | GRCh38.p7 | 5:65579641 | ACTAGGAGATTAGAC[A/G]GTAATGTTCCTTCCA | 23398 |
| rs373820233 | snp | C/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65581709 | TACTTGTGTGTTGAT[C/T]AAAGTATATATATTC | 23398 |
| rs373825399 | snp | C/T | 3.30841e-05 | 0.00406706 | missense, intron-variant | PPWD1 | GRCh38.p7 | 5:65572176 | TATCCAACCAGCGTA[C/T]GTTTTTCACCAGATG | 23398 |
| rs373879376 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PPWD1 | GRCh38.p7 | 5:65583334 | AAGGAATTTTGAAGA[A/C]ACGTTTGATAAAAAA | 23398 |
| rs373950730 | snp | A/G | 0.000162694 | 0.0090178 | upstream-variant-2KB, intron-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65563529 | CAGACATAGTACCGG[A/G]ACGAATTGGAGTGCT | 23398 |
| rs374067564 | snp | A/G | 0.000153988 | 0.00877328 | splice-donor-variant | PPWD1 | GRCh38.p7 | 5:65577070 | TGTAGAGACAAACCG[A/G]TAAGCTTTAATATGA | 23398 |
| rs374115016 | snp | A/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65573189 | CCCTCCCTCCTCATA[A/T]TCCTCCATTACCTAT | 23398 |
| rs374262962 | snp | C/T | 1.70691e-05 | 0.00292134 | intron-variant | PPWD1 | GRCh38.p7 | 5:65577088 | AGCTTTAATATGAGG[C/T]ATGTTTTTTAAAAAT | 23398 |
| rs374315096 | snp | A/G | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65572497 | GCGTTTTTCAAGTCA[A/G]TTATTGTCTTATTTT | 23398 |
| rs374361968 | in-del | -/GATATA | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65576821 | ATAGATAGATGGGTT[-/GATATA]GATATAGGTATATGT | 23398 |
| rs374631833 | snp | A/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65576119 | TCTCAATTTTTTATA[A/T]TGTTGAGATGATATT | 23398 |
| rs374709025 | snp | G/T | | | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65562018 | GATTTCAGGTAGTCA[G/T]AAGTGCTATGAAATG | 23398 |
| rs374764627 | in-del | -/TTTTTTTTTTTTTTTTTTTTTA | 0.131723 | 0.220251 | intron-variant | PPWD1 | GRCh38.p7 | 5:65573533 | TTTTTTTTTTTTTTT[-/TTTTTTTTTTTTTTTTTTTTTA]AGTACAGACGGGTTT | 23398 |
| rs375043805 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPWD1 | GRCh38.p7 | 5:65574743 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC | 23398 |
| rs375281263 | snp | A/C/T | 0.000476684 | 0.0154312 | intron-variant | PPWD1 | GRCh38.p7 | 5:65569588 | ATACTAAGTGATTCA[A/C/T]AGATCTGTCTTAGAA | 23398 |
| rs375310583 | snp | A/G | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65572655 | CTTCTCTAACCTTCT[A/G]TTACAAGCAAACCTG | 23398 |
| rs375586974 | snp | A/G | 1.66574e-05 | 0.0028859 | intron-variant | PPWD1 | GRCh38.p7 | 5:65569830 | GAATCATGCACACTT[A/G]TTTTACTGTTATTTA | 23398 |
| rs375762851 | snp | C/G/T | 4.03429e-05 | 0.00449108 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65567491 | TAAAAATAGATCTTA[C/G/T]ACTTTACTTTTTTTT | 23398 |
| rs375857453 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65566614 | CCTGAAACAGCTCGT[C/T]ATGTTTAATTTAGCA | 23398 |
| rs375988025 | in-del | -/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65580082 | GTGGAATTTTTTTTT[-/T]CTCTTCTGGAGAACT | 23398 |
| rs376014526 | snp | C/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65579236 | TTCTGTTTTTTAACC[C/T]GAAAATTATAGCTGC | 23398 |
| rs376016161 | snp | A/C/G | 3.36424e-05 | 0.00410125 | missense | PPWD1 | GRCh38.p7 | 5:65586164 | GGATCCCAGTTTTTC[A/C/G]TAACGGTAGTACCAA | 23398 |
| rs376030448 | snp | C/T | 0.00636936 | 0.0560724 | upstream-variant-2KB, intron-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65564452 | TCCTGCCTCAGCCTC[C/T]CGAGTAGCTGGGGCT | 23398 |
| rs376230707 | snp | A/C | 0.00014834 | 0.00861092 | upstream-variant-2KB, utr-variant-5-prime, missense | CENPK, PPWD1 | GRCh38.p7 | 5:65563394 | AAAAACAGAACTCAG[A/C]GAAAGAGAGCTGGCA | 23398 |
| rs376289595 | snp | G/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65574598 | CCTCCCGAGTAGCTG[G/T]GACTACAGGCGCCCG | 23398 |
| rs376380239 | snp | C/G/T | 0.000301935 | 0.0122833 | missense | PPWD1 | GRCh38.p7 | 5:65583063 | GAGAACCAGAAGATA[C/G/T]GAAAAGTGCAGATTC | 23398 |
| rs376504285 | snp | C/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65586513 | TTAGAATACAAAGAT[C/T]AGAGTATATGAATTC | 23398 |
| rs376567769 | snp | A/C/G | 0.000137709 | 0.00829681 | intron-variant | PPWD1 | GRCh38.p7 | 5:65585948 | ATAAAACTTCAAAGC[A/C/G]TACATATATCGAAAA | 23398 |
| rs376582408 | snp | C/G | 1.65233e-05 | 0.00287426 | synonymous-codon, intron-variant | PPWD1 | GRCh38.p7 | 5:65572148 | TTTATATGAATTTGC[C/G]AAGTGTAAGGCTTAT | 23398 |
| rs376744565 | snp | A/C | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65579234 | ATTTCTGTTTTTTAA[A/C]CTGAAAATTATAGCT | 23398 |
| rs376755497 | snp | A/G | 7.34026e-05 | 0.00605771 | intron-variant | PPWD1 | GRCh38.p7 | 5:65583008 | TGAAAACTTTAATTC[A/G]TTGACTCACTTTTTA | 23398 |
| rs376852229 | snp | C/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65578773 | GTGTATATATATATA[C/T]ATATATATGTGTATA | 23398 |
| rs376868315 | snp | G/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65576115 | GTTATCTCAATTTTT[G/T]ATATTGTTGAGATGA | 23398 |
| rs377013321 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPWD1 | GRCh38.p7 | 5:65569136 | ATGATTTCTATTTTT[A/G]CATACCTAATAGGAA | 23398 |
| rs377093252 | snp | C/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65578797 | GTGTATATATATATA[C/T]ATATATATGTGTATA | 23398 |
| rs377143602 | snp | C/G | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65570662 | TGGAAAGTCCAAGAT[C/G]AAGGTTCCATCAGGG | 23398 |
| rs377239494 | snp | C/G | 9.07087e-05 | 0.00673395 | intron-variant | PPWD1 | GRCh38.p7 | 5:65569601 | CATAGATCTGTCTTA[C/G]AAATTAACTTTTAAC | 23398 |
| rs377267023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65581552 | GATCACACCACTGCA[C/T]TTCAGCCTAGGTGAC | 23398 |
| rs377268275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65579006 | TCACAACCTCTGCCT[C/T]CTGAGTTCAAGTGAT | 23398 |
| rs377360663 | snp | G/T | 1.65518e-05 | 0.00287674 | synonymous-codon, intron-variant | PPWD1 | GRCh38.p7 | 5:65571896 | TGCAATTTCTTCAGT[G/T]GCTGCTTCCGAAAAG | 23398 |
| rs377442178 | snp | C/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65579965 | TACTCTTGAATATAA[C/T]TTATCTTCCCCAAAT | 23398 |
| rs377505721 | snp | G/T | | | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65568079 | TAGTTTTTGAGTGCT[G/T]AACATGATACTCAAA | 23398 |
| rs377508764 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | PPWD1 | GRCh38.p7 | 5:65576842 | GATATAGGTATATGT[A/G]TATAGAGTTTTTGTT | 23398 |
| rs377652689 | snp | A/G | 1.67158e-05 | 0.00289096 | intron-variant | PPWD1 | GRCh38.p7 | 5:65569742 | ACCTGGGTAAGAATT[A/G]CACCTCATTTTCTTG | 23398 |
| rs386403981 | in-del | -/A | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65584883 | AGAGATTATGAAAAA[-/A]AAAAAACAACTGTCC | 23398 |
| rs386688654 | in-del | A/TGG | | | upstream-variant-2KB, intron-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65564060 | AAAACCCGAAGTCTG[A/TGG]TTTTGAAATCACGCT | 23398 |
| rs386688656 | multinucleotide-polymorphism | CG/TA | | | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65566375 | TAAGATTACAGCAGT[CG/TA]TATCCCAGTTCCAAG | 23398 |
| rs386688657 | multinucleotide-polymorphism | AAA/TTT | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65569090 | TAAGGTAATATGTAC[AAA/TTT]GTACCTGACATATAC | 23398 |
| rs397998012 | in-del | -/T | 0 | 0 | intron-variant | PPWD1 | GRCh38.p7 | 5:65565826 | GAATAAACTATTGGC[-/T]TTTTTTTTTTTTTTT | 23398 |
| rs397998013 | in-del | -/A | 0 | 0 | intron-variant | PPWD1 | GRCh38.p7 | 5:65573190 | AATAGGTAATGGAGG[-/A]ATATGAGGAGGGAGG | 23398 |
| rs397998014 | in-del | -/T | 0 | 0 | intron-variant | PPWD1 | GRCh38.p7 | 5:65579233 | GCTATAATTTTCAGG[-/T]TTAAAAAACAGAAAT | 23398 |
| rs398109014 | in-del | -/A | | | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65567670 | TTAAAAAAAAAAAAA[-/A]GCTTCAATTTTGAGG | 23398 |
| rs398109015 | in-del | -/A/TATACACACATATATGTGTATAT | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65578742 | ATATATACATATATA[-/A/TATACACACATATATGTGTATAT]TATACACACATATAT | 23398 |
| rs527416629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65585867 | AATTTAAGTGTTAAG[A/G]GTTTAATCAAATCAC | 23398 |
| rs527455006 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PPWD1 | GRCh38.p7 | 5:65579227 | TGGCCTCATTTCTGT[G/T]TTTTAACCTGAAAAT | 23398 |
| rs527503386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65578882 | TATGAGCCGTTCTCC[C/T]AGTCTGTGACTTTTC | 23398 |
| rs527516579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65586660 | ATAAAAATTACCTAG[C/T]TTTTGTTTTGGAATT | 23398 |
| rs527560777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65573220 | TGAACTGGTACTTCA[A/G]ATTTCAAATGAAGAG | 23398 |
| rs527564540 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65564393 | GCATGCAGTGGCGCT[A/G]TCTCGGCTCACCGCA | 23398 |
| rs527626328 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPWD1 | GRCh38.p7 | 5:65572436 | CAACTGTTTCTGTCT[C/T]GTAGTGTTGCTCTTT | 23398 |
| rs527796996 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | PPWD1 | GRCh38.p7 | 5:65580681 | ACCATACCCAGCTAA[G/T]TTTTGTATTTTTAGT | 23398 |
| rs527885596 | snp | C/G | 0.000798403 | 0.0199641 | downstream-variant-500B | PPWD1 | GRCh38.p7 | 5:65587818 | TATACTGCTATAGTT[C/G]TTCTATTTTATTGTT | 23398 |
| rs528049023 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PPWD1 | GRCh38.p7 | 5:65574480 | TTTTTTTTTTGAGAC[A/G]GAGTCTCGCCCTGTT | 23398 |
| rs528106132 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PPWD1 | GRCh38.p7 | 5:65570800 | TTATAAGGCTACAAG[C/G]CCATCAGATTAGGAC | 23398 |
| rs528126898 | snp | C/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65580271 | TTTTTAAGACCCAAA[C/T]GTGACTCTTATTTTC | 23398 |
| rs528241205 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPWD1 | GRCh38.p7 | 5:65574762 | GCCACCGCGCCCGGC[C/T]GGCACAAATCTCTTA | 23398 |
| rs528615521 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPWD1 | GRCh38.p7 | 5:65582676 | CCAAACAATCTAAAT[A/G]ATGAACTGAGCAACA | 23398 |
| rs528743925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65561460 | TAAGAGTTTGCTCTC[C/T]ACCGCTTGAGGATGC | 23398 |
| rs529132123 | snp | A/C | | | upstream-variant-2KB, missense, utr-variant-5-prime, synonymous-codon | CENPK, PPWD1 | GRCh38.p7 | 5:65563484 | TTTACCTGTGGAGGC[A/C]ACACTGGCCAAGAAG | 23398 |
| rs529208529 | snp | C/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65586465 | GTAACCTAAAATAAA[C/T]TATTTCACTTCTGTG | 23398 |
| rs529228910 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PPWD1 | GRCh38.p7 | 5:65578827 | ATATATACTTTTTTT[A/T]AAAAAAAGAGTTTTT | 23398 |
| rs529249412 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65570145 | TTGGAAAATTAGATA[C/G]AGCGAAGCCTTATAA | 23398 |
| rs529269644 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65585642 | ATTAGCGAAAAGGCT[G/T]TCCAGGAAATCCAGA | 23398 |
| rs529417218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65570975 | TCAGTTTATGACTTT[A/G]TGAGCCACTAAAGGA | 23398 |
| rs529426676 | in-del | -/GAG | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65562649 | ATGAAGAAGACAGAT[-/GAG]GAGGAGGAGGAGAAA | 23398 |
| rs529711004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65586995 | TAACTTACCTTTAGG[A/G]AAGATCTTCCAGTTC | 23398 |
| rs529811899 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PPWD1 | GRCh38.p7 | 5:65573314 | TTTATTTATTTAATT[A/T]ATTTATTTTCTGAGA | 23398 |
| rs529868113 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PPWD1 | GRCh38.p7 | 5:65580250 | TTCACAATGGAATCA[C/G]AGAACTTTTTAAGAC | 23398 |
| rs529925756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65566192 | CTACAGAAAAACCCA[A/G]AATAACGATGTTGAA | 23398 |
| rs529985849 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPWD1 | GRCh38.p7 | 5:65565359 | CTTTTTTAATTAAAC[A/G]AGTAAGGAGAAATGT | 23398 |
| rs530053015 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPWD1 | GRCh38.p7 | 5:65574233 | TCTGTTTGCCAGCCA[A/G]ATTATCCTTATGACA | 23398 |
| rs530104494 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65579840 | TTCAACCTCGTTTCC[A/C]CAACTATTTGTGTTG | 23398 |
| rs530361001 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65581935 | ATATATGAGCTAAAT[A/C]ATAATTTTTCAGATC | 23398 |
| rs530486750 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | PPWD1 | GRCh38.p7 | 5:65575520 | TAGAAAACACAAGAT[G/T]ATGGTTAATATAAGC | 23398 |
| rs530699132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65561254 | AGTCATCATGAATTT[C/T]AGAATATTTTTAAGC | 23398 |
| rs530881790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65583571 | CTCAAAGCAAATCCT[C/T]AAGAGAAAGATAATT | 23398 |
| rs531003641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65577665 | GAACAGTTAACAGAC[A/G]TGGAATTTTAATAAG | 23398 |
| rs531067075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65584154 | CATTTTGAATATGAA[C/T]GTTTTATACCATATC | 23398 |
| rs531098877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65569391 | TAATGTCAAATTCTA[A/G]TTCAATTCTGATCCT | 23398 |
| rs531123073 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPWD1 | GRCh38.p7 | 5:65577935 | GGTGTTGTATATTCT[A/G]TAGGTTTGGAGAAAT | 23398 |
| rs531360139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65585814 | TGCATTTATGTTTCA[A/G]TCAAGGTGGTGGTTG | 23398 |
| rs531482397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65579169 | TGATCTGCCTGCCTC[A/G]GCCTCCCAAAGTGCT | 23398 |
| rs531527135 | in-del | -/A/AA | 0.0317497 | 0.121966 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65567657 | GTTCTGAGTTTATTT[-/A/AA]AAAAAAAAAAAAAGC | 23398 |
| rs531531419 | snp | C/T | | | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65561435 | TAGAATAAAAACATA[C/T]AGAAACATTTAAGAG | 23398 |
| rs531609347 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65571268 | TTGAGTGTTTTAGTA[C/G]AATTGATTAGATCAG | 23398 |
| rs531715661 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65564229 | GTTTTCCTTAAGTAT[C/T]TAAGACATTTTAAAT | 23398 |
| rs532025887 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | PPWD1 | GRCh38.p7 | 5:65587613 | AAATGGACTAAACTC[A/G]GGCAAATAGCACTCA | 23398 |
| rs532095437 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65580406 | ATACTGAAAGTTCAC[A/T]TGTAGTTGAGTGTGC | 23398 |
| rs532195758 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | PPWD1 | GRCh38.p7 | 5:65574505 | CCTGTTGCCCAGGCC[A/G]GACTGCGGACTGTAG | 23398 |
| rs532221679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65574378 | AATTTTAAAATTCTA[C/T]TAACTTGCAGCTCTT | 23398 |
| rs532287890 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65573504 | AGAGATGGGTTTTTT[A/T]TAGTACAGATGGTTT | 23398 |
| rs532647968 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPWD1 | GRCh38.p7 | 5:65576478 | GCCTCCTAGGTTCAA[A/G]CGATTCTCTTGCCCC | 23398 |
| rs532676844 | snp | A/T | 0.0158835 | 0.0876895 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65567658 | GTTCTGAGTTTATTT[A/T]AAAAAAAAAAAAGCT | 23398 |
| rs532710228 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65575654 | AAAGAATGTAAAGAT[C/G]GTTACTCTTTTGGAA | 23398 |
| rs533361577 | snp | C/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65571393 | AGTGTTTTTCTTTGA[C/T]GTATTGTCATAATAA | 23398 |
| rs533378566 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65584285 | TGGGTACAAGATTCT[A/C]TTGGTTCGTCCATTT | 23398 |
| rs533463087 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | CENPK, PPWD1 | GRCh38.p7 | 5:65563256 | AAGACTGCGCCGCTG[C/T]TTTGGGATTGGTAGC | 23398 |
| rs533535825 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | CENPK, PPWD1 | GRCh38.p7 | 5:65562965 | GTTGGCGCGCGGGAA[A/G]CCGAGAAGAACGGGA | 23398 |
| rs533542364 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PPWD1 | GRCh38.p7 | 5:65578129 | AGATTGGCTCCTTTC[A/G]GTAATATGCATTTAA | 23398 |
| rs533636359 | snp | A/C/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65582545 | GACTTAATATCTATT[A/C/T]GTTTAATCTTCACAA | 23398 |
| rs533737818 | in-del | -/TT | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65569222 | GGATATAAAAAAAAC[-/TT]TTGTTGAATTTTGTT | 23398 |
| rs533759262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65570532 | GTCAGCTTGAAAGTC[A/G]TAACAGTGTCAGAAA | 23398 |
| rs533795985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65584530 | ACCTATACTACTACA[C/T]GCAGACCTATAATAC | 23398 |
| rs534069130 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PPWD1 | GRCh38.p7 | 5:65578786 | TACATATATATGTGT[A/G]TATATATATACATAT | 23398 |
| rs534130628 | snp | A/T | 1.81089e-05 | 0.00300901 | stop-gained | PPWD1 | GRCh38.p7 | 5:65579602 | TCATTCAAAAAGAAT[A/T]GATTTTATATGGTAT | 23398 |
| rs534269282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65586286 | TTTTCTGCATTATTT[A/G]TATCATCTAGCAGAA | 23398 |
| rs534351652 | in-del | -/AAAC | 0.00199481 | 0.0315187 | intron-variant | PPWD1 | GRCh38.p7 | 5:65581587 | CAAGACCCTATTGCT[-/AAAC]AAAAACAGGCAAAAA | 23398 |
| rs534491631 | snp | A/G | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65566314 | CCAGCTTTCTGCCCA[A/G]CATAACTAAGGTACA | 23398 |
| rs534528629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65572761 | TCCTTAACTCTTTTA[C/T]CCTTCTGTGTAATTC | 23398 |
| rs534716015 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PPWD1 | GRCh38.p7 | 5:65581524 | CAACGAATTCAAGGT[G/T]GCAGTGAGCTATGAT | 23398 |
| rs534774994 | in-del | -/TTAAA | 0.00119737 | 0.0244387 | intron-variant | PPWD1 | GRCh38.p7 | 5:65587166 | AAGGGGAGCGTAAAC[-/TTAAA]TTCTCTTTAATTTGC | 23398 |
| rs535420175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65577843 | TATCAACGTCCCCCA[C/T]CAGAGTGGTCCATTT | 23398 |
| rs535484911 | snp | G/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65584221 | TTGGACAGTCTCACT[G/T]TAAGTGCTCAAAACC | 23398 |
| rs535647361 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | PPWD1 | GRCh38.p7 | 5:65583792 | TATCTCTTAAAAAAA[A/T]TTTTTTTTTATTAGC | 23398 |
| rs535716166 | in-del | -/A | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65561831 | ATACATGAAATAAGC[-/A]AAAAAATACCCACAT | 23398 |
| rs535868099 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPWD1 | GRCh38.p7 | 5:65578942 | GTTTTTTATTGAGAT[A/G]GAGTCTTGTTCTGTC | 23398 |
| rs535876382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65561948 | TCTTTGTACTTGTAG[A/G]GCTTCCATTCTCATG | 23398 |
| rs535998091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65571771 | ACATTTTTGGTAGTG[A/G]GATAGGGAGGGATGC | 23398 |
| rs536001784 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65564423 | AACCTCCGTCTCCGG[A/G]GTTCAAGCGATTCTC | 23398 |
| rs536262156 | snp | C/T | 1.65233e-05 | 0.00287426 | synonymous-codon | PPWD1 | GRCh38.p7 | 5:65586022 | GATTCAGACTGGAGA[C/T]CCAACAGGTACTGGT | 23398 |
| rs536375204 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | PPWD1 | GRCh38.p7 | 5:65588015 | TACACAACTGTGCTT[C/T]AATTTTGAATACCTG | 23398 |
| rs536465101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65580628 | CAGCAATTCGCCTGC[C/T]TCAGTCTCCTGGGTA | 23398 |
| rs536469877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65572480 | CTAGGGGTTTATGAT[A/G]TGCGTTTTTCAAGTC | 23398 |
| rs536484149 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | PPWD1 | GRCh38.p7 | 5:65586582 | TGAAATCAGAATACA[G/T]TAGATTTGATGAAAT | 23398 |
| rs536584473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65565851 | TTATTCAGTTTGAAG[A/G]AAAAAATTGAAACTA | 23398 |
| rs536783281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65579671 | AGTTTGGTTTGACTT[C/T]TCTTTGTTTGTACCT | 23398 |
| rs536929434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65566518 | AGAAAGGTCATGTTA[C/T]ATCTGGACATCAGTA | 23398 |
| rs537080450 | snp | C/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65565993 | GACATTGGACTGTTG[C/T]ATATATTTTCAGAAA | 23398 |
| rs537373423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65582176 | GAGGCACTAGCTTTA[C/T]GTTCCCATAATTAAG | 23398 |
| rs537436263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65583909 | GTTAGCTATGGTCAA[A/G]CCACTGCACTCCAAC | 23398 |
| rs537575934 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPWD1 | GRCh38.p7 | 5:65584477 | TCGCTGTAGCATAAC[A/G]ATGCTTTTGTAAGAA | 23398 |
| rs537604829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65578460 | TCCCACCAGCAATGA[A/G]TGAGTGTTCCTGTCA | 23398 |
| rs537668517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65578083 | TTCCAGAATGTGATA[C/T]AGCTAAAATCATACA | 23398 |
| rs537709336 | snp | A/G | | | missense, intron-variant | PPWD1 | GRCh38.p7 | 5:65572191 | TGTTTTTCACCAGAT[A/G]GGAAGAAAATAGCTA | 23398 |
| rs537789420 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPWD1 | GRCh38.p7 | 5:65570399 | TTATTGGTGACTTTA[A/C]ACTTTGGAATATATT | 23398 |
| rs538368094 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | PPWD1 | GRCh38.p7 | 5:65577319 | TCAAGTTGTTGTGTG[-/T]TTTTTTTTAACAAGT | 23398 |
| rs538430674 | snp | A/C/G | 0.000138929 | 0.00833346 | intron-variant | PPWD1 | GRCh38.p7 | 5:65586185 | GTAGTACCAACGGTA[A/C/G]GTACAGTATCATTGT | 23398 |
| rs538555962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65587041 | ATGCAGATATTTAAT[C/T]AAACATTATACTATG | 23398 |
| rs538565296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65578982 | GGAGAGCAGTGGCAC[A/G]ATCTCGGCTCACAAC | 23398 |
| rs538593871 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65572635 | TATGACTACTTCTAA[A/C]TTTACTTCTCTAACC | 23398 |
| rs538645758 | snp | A/T | 1.74024e-05 | 0.00294972 | intron-variant | PPWD1 | GRCh38.p7 | 5:65571809 | TTGTGCTGACCTTTT[A/T]TTTTCCCTCTCAATT | 23398 |
| rs538651392 | snp | A/G | 8.27164e-05 | 0.0064305 | missense | PPWD1 | GRCh38.p7 | 5:65579509 | AAAAAGCATCGTGCT[A/G]CAACTACTATAGAAA | 23398 |
| rs538706544 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PPWD1 | GRCh38.p7 | 5:65565568 | TGGCACTTTGGGAGG[C/G]TGAGGCGGGCAGATC | 23398 |
| rs538767971 | snp | C/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65573160 | ATAAGTTGTTTCCTC[C/T]ACCTGGAGTGAGGCC | 23398 |
| rs538775054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65581468 | GTGTGCACATGTGGT[C/T]TCAGCCATGCTGGAA | 23398 |
| rs539475644 | snp | C/T | | | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65562415 | AAAATAAAGTGCCTA[C/T]TATGGGGGGGCAGTT | 23398 |
| rs539531439 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65562370 | GAGACTTGCTAGGTA[C/G]AATGGTCAAATAATG | 23398 |
| rs539532124 | snp | C/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65584463 | TGGCCAAGAGTATGT[C/T]GCTGTAGCATAACAA | 23398 |
| rs539778251 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65576163 | GTTTAATCAAACATT[A/T]AAATGAAATTCACCT | 23398 |
| rs539849798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65577302 | AAGAAGATATGCATA[A/G]TTTCAAGTTGTTGTG | 23398 |
| rs539851844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65581148 | CCCAACCAACCTTCC[A/G]TCTAAATGGGTAAAT | 23398 |
| rs539862953 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65576733 | CATATTGTTTAGAAT[A/C]CCTCTTAAGAAGTAC | 23398 |
| rs539910496 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PPWD1 | GRCh38.p7 | 5:65573132 | AACCTGCCTCCCACC[A/G]CAGGACCTTTTTATA | 23398 |
| rs539964544 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65561773 | TATTTAGGGATAATA[A/C]TATACTTAAAGAAAC | 23398 |
| rs540075556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65562733 | AGTGACCCGTTCTGC[C/T]CTAGGTCTTTTGGTT | 23398 |
| rs540356825 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65562144 | TAATAAATGTTAACT[A/T]GCTACATTATTATTA | 23398 |
| rs540852132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65580102 | TCTGGAGAACTAAAA[A/G]TACTTTGCATGTTAA | 23398 |
| rs540906780 | snp | A/C | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65579301 | AGAAACACTTTTAAA[A/C]ATCTTTCACTAGTTA | 23398 |
| rs541038330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65574200 | CTGAAGTAATATATT[C/T]CCAGACAAATGTGAA | 23398 |
| rs541165177 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65566655 | GGCACGTTTGGTCAT[C/T]GTTCAGTTATTTTAT | 23398 |
| rs541669196 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPWD1 | GRCh38.p7 | 5:65576263 | ATTGGAAAGTGCTAC[C/T]CTGTGACTTTTAAAA | 23398 |
| rs541800494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65582362 | TTCTCCTATGCTTCA[A/G]GGTTTAGATTCTAGG | 23398 |
| rs541973496 | in-del | -/AC | 0.106181 | 0.20449 | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65561601 | GTTTAATTAAAACAC[-/AC]ACACACACACACACA | 23398 |
| rs542056483 | snp | A/T | 1.78905e-05 | 0.00299081 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65567501 | TCTTATACTTTACTT[A/T]TTTTTCTTCAGTCTT | 23398 |
| rs542167371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | CENPK, PPWD1 | GRCh38.p7 | 5:65562852 | TCAGGAGAGAAAACA[C/T]GTTTAGTGCATCTGA | 23398 |
| rs542274062 | snp | C/T | 1.67556e-05 | 0.0028944 | missense, intron-variant, utr-variant-5-prime | PPWD1 | GRCh38.p7 | 5:65569994 | ATCAACATGCTGAAA[C/T]TTGGGTGAGTCTTTT | 23398 |
| rs542352928 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65563155 | GGAAGCGCTTGCCAG[C/G]CCCGGACTTCTGCGC | 23398 |
| rs542392824 | snp | C/T | 0.00223505 | 0.0333546 | intron-variant | PPWD1 | GRCh38.p7 | 5:65570022 | TTTTAAAAGTATATA[C/T]ATTTTAACTTATTGA | 23398 |
| rs542432307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65584627 | TTTAGGAGGCTGAGG[C/T]AGGAGGATGTCTTGA | 23398 |
| rs542537433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65569271 | GTTTAGATTTACTTA[C/T]CAGCTACTGACAAAT | 23398 |
| rs542618889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65586505 | CCTTGTCTTTAGAAT[A/G]CAAAGATTAGAGTAT | 23398 |
| rs542648710 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPWD1 | GRCh38.p7 | 5:65579145 | TGGTCTCGAACTCCT[A/G]ACCTCAAGTGATCTG | 23398 |
| rs543014065 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65578828 | TATATACTTTTTTTT[A/T]AAAAAAGAGTTTTTT | 23398 |
| rs543196073 | snp | A/G | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65578055 | CTTTTCACCATCTCC[A/G]TAGTTTTGCCTCTTC | 23398 |
| rs543257108 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65564147 | TTATCAAATAAAAGG[A/G]GTGGGAAAAGGGGTA | 23398 |
| rs543402889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65567357 | GACGTTAAAACTGAG[A/G]TAACATACTGGATTT | 23398 |
| rs543418334 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | PPWD1 | GRCh38.p7 | 5:65587576 | TCTCGCAATATTTCT[A/G]ATCCTGGGAGGTGAT | 23398 |
| rs543635491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65581607 | AAAACAGGCAAAAAA[A/G]GATATTTCTTGATAT | 23398 |
| rs543643469 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65581093 | AATGCTATTAAGGTT[A/C]ACAGCATTTGATAAA | 23398 |
| rs543672766 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65582424 | CCATTTCAGATTCAT[G/T]TTTGTGAATCCTTAT | 23398 |
| rs543805740 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65583342 | TTGAAGAAACGTTTG[A/T]TAAAAAACATCTATT | 23398 |
| rs543841056 | in-del | -/ATAG | | | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65567481 | GTTTATTTGTTAAAA[-/ATAG]ATCTTATACTTTACT | 23398 |
| rs543933775 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPWD1 | GRCh38.p7 | 5:65577131 | GACCATTTCCTCCAT[C/T]ATGGGAACAGTGGGA | 23398 |
| rs544277772 | snp | C/G | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65577797 | GATTTTCCATATACC[C/G]TCTGCCCCAACACAT | 23398 |
| rs544522482 | snp | C/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65582862 | TTTCATATTAGACAA[C/T]GTAAAAATAATTTAA | 23398 |
| rs544681683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65584840 | AAGAATATACTACTT[A/G]CATGACCCTCCGTGC | 23398 |
| rs544694749 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65563228 | ATCCCGAAACTCGCT[C/T]GGACGCTGACAGAAG | 23398 |
| rs544822124 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PPWD1 | GRCh38.p7 | 5:65578282 | AAGTTTTGGCAGTTA[C/T]GTATAAAAGCTGCTA | 23398 |
| rs544861184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65586616 | GTATAAGGTAACCTA[A/G]CTCTATTGCTATGCC | 23398 |
| rs544946463 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65563869 | ACCAGTTCTCTTTAA[A/G]GCTTTAGTTCAGGAG | 23398 |
| rs544998248 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65573201 | ATATTCCTCCATTAC[A/C]TATTGAACTGGTACT | 23398 |
| rs545012378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65579816 | GTTTTCCATCATGTT[C/T]TGAAATTTTTCAACC | 23398 |
| rs545600019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65566064 | TGTGTTTTACTCTTC[C/T]TTATGCCCATGTGAC | 23398 |
| rs545690156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65582208 | TACATCAGATAGAGG[C/T]TGCTTAGGAGAGAGC | 23398 |
| rs545888984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65581743 | ATAAAGTTTGAAAAA[A/G]TAGAGAAACAAAATA | 23398 |
| rs546028090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65574759 | TGAGCCACCGCGCCC[A/G]GCCGGCACAAATCTC | 23398 |
| rs546199365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | PPWD1 | GRCh38.p7 | 5:65568486 | TTTTTATTTCTTGTA[C/T]GGGTTTTGAACCTGT | 23398 |
| rs546274675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65561386 | AGGGATAAATATTCA[A/G]CAAATTATCTGGCTT | 23398 |
| rs546299830 | snp | A/G/T | 6.79129e-05 | 0.00582682 | intron-variant | PPWD1 | GRCh38.p7 | 5:65585977 | AAGGACAATGTAATG[A/G/T]TTTTGTGTACTTTCT | 23398 |
| rs546312456 | snp | G/T | | | intron-variant, utr-variant-5-prime | PPWD1 | GRCh38.p7 | 5:65568839 | CAAGTTATCAGTGTG[G/T]TAAAACAGTATATAT | 23398 |
| rs546360983 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65583408 | GGAAATTTTTATGCA[G/T]ATATACTTTATAGGT | 23398 |
| rs546474112 | snp | C/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65571208 | TGGTTAGAATAATAG[C/T]GTCACTTCTCCGAAT | 23398 |
| rs546485823 | snp | A/G | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65565340 | ATGAATATTTTTGCA[A/G]GTTCTTTTTTAATTA | 23398 |
| rs546536358 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65584370 | TTCAGTTAATATTAT[G/T]GAGAAAGCTTCGTAC | 23398 |
| rs546684178 | snp | A/G | | | missense, utr-variant-5-prime, intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65567534 | AGTTTGAAAGAGTCT[A/G]TCTTGATAATCTCCC | 23398 |
| rs546949310 | in-del | -/T/TG | | | upstream-variant-2KB, intron-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65564060 | AAAACCCGAAGTCTG[-/T/TG]GTTTTGAAATCACGC | 23398 |
| rs547001816 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65569518 | AAGAAGGGTTTTTTT[A/T]AAAAAAAAACCTATT | 23398 |
| rs547045940 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65562424 | TGCCTACTATGGGGG[C/G]GCAGTTCCTTCCCTG | 23398 |
| rs547057562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65585944 | AGAAATAAAACTTCA[A/G]AGCGTACATATATCG | 23398 |
| rs547064611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65577804 | CATATACCCTCTGCC[C/T]CAACACATGCATAGC | 23398 |
| rs547173896 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPWD1 | GRCh38.p7 | 5:65572457 | GTTGCTCTTTGAAAG[C/T]CTCTTCTCTAGGGGT | 23398 |
| rs547192085 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPWD1 | GRCh38.p7 | 5:65571756 | AAATCACCAGCCAAG[A/G]CATTTTTGGTAGTGG | 23398 |
| rs547228205 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | CENPK, PPWD1 | GRCh38.p7 | 5:65562968 | GGCGCGCGGGAAGCC[A/G]AGAAGAACGGGACTC | 23398 |
| rs547378577 | snp | C/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65586713 | GAAAAATGTAACTAC[C/T]ATCTGCCAGGCACAT | 23398 |
| rs547397376 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65565252 | TTCATTGCTTGGTGT[A/C]CAGTGCTTTGCCTAA | 23398 |
| rs547411232 | snp | A/G | 5.92037e-05 | 0.00544044 | utr-variant-3-prime | PPWD1 | GRCh38.p7 | 5:65587421 | TGTTTTAATGTACTT[A/G]CAAATAAAAATACAA | 23398 |
| rs547428460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65586714 | AAAAATGTAACTACC[A/G]TCTGCCAGGCACATA | 23398 |
| rs547655054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65580574 | GCTAGAGTGCAGTGA[C/T]GTGACTTCAGCTCAC | 23398 |
| rs547738015 | in-del | -/ATTATC | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65562156 | ACTAGCTACATTATT[-/ATTATC]ATTATCATTATCATC | 23398 |
| rs547867481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65574801 | ACTCTGAGCTGCTCA[A/G]TCCACTCTATTTGCT | 23398 |
| rs547975624 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | PPWD1 | GRCh38.p7 | 5:65585559 | GGATGGGGCACTGAT[-/A]ACAGTGCTTGGTTTC | 23398 |
| rs548265710 | snp | C/T | 3.30028e-05 | 0.00406205 | synonymous-codon | PPWD1 | GRCh38.p7 | 5:65583106 | TTTTAATGAGAAACC[C/T]TCTAAAGAAGAAGTC | 23398 |
| rs548332051 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65566984 | TAGGATGTTCTCAGG[C/T]ATAAAAATCTAAGAA | 23398 |
| rs548361151 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPWD1 | GRCh38.p7 | 5:65583467 | TGAAAGTGCTGAGTG[C/T]AAACTGTAAAGTGAT | 23398 |
| rs548498664 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPWD1 | GRCh38.p7 | 5:65576567 | GTTTTTAGTGGAGAC[A/G]GGGTTTCACCATGTT | 23398 |
| rs548499564 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65561564 | TCTCCAGCCTCTAGA[C/T]CTGTGAGAAATAAAT | 23398 |
| rs548523890 | snp | A/G | | | intron-variant, utr-variant-5-prime | PPWD1 | GRCh38.p7 | 5:65568467 | GGGCTAAATCCTAGA[A/G]GACTTTTTATTTCTT | 23398 |
| rs548544945 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65582699 | GAGCAACAAACAGGT[G/T]GCATGTTAGGCCTTA | 23398 |
| rs548627320 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPWD1 | GRCh38.p7 | 5:65575924 | ATTGAGTGCTTGTTA[C/T]GTCAGGCACGTAACC | 23398 |
| rs548804600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65584456 | AAGGTTTTGGCCAAG[A/G]GTATGTCGCTGTAGC | 23398 |
| rs549525192 | snp | A/G | 0.00158209 | 0.028081 | upstream-variant-2KB, utr-variant-5-prime, missense | CENPK, PPWD1 | GRCh38.p7 | 5:65563357 | AGAGACGTAGAAGGC[A/G]CCGGGACCCGGAGGA | 23398 |
| rs549663779 | snp | A/C | | | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65561439 | ATAAAAACATATAGA[A/C]ACATTTAAGAGTTTG | 23398 |
| rs549723682 | snp | G/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65572419 | AGCACATTAGAGATA[G/T]TCAACTGTTTCTGTC | 23398 |
| rs549779847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65579335 | TGTACATAGATAAGA[C/T]AGTTGATTCCCAGCT | 23398 |
| rs549939903 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPWD1 | GRCh38.p7 | 5:65581945 | TAAATCATAATTTTT[C/T]AGATCCAACATCATG | 23398 |
| rs550091446 | snp | C/G | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65586250 | AGAGTGAACTCAGTA[C/G]AAGAGCTGCATTATT | 23398 |
| rs550297856 | snp | A/C/T | 3.30438e-05 | 0.0040646 | missense, synonymous-codon, intron-variant, utr-variant-5-prime, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65567569 | GCATCCATGTATGAG[A/C/T]GCAGTTACATGCATA | 23398 |
| rs550554534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65567092 | ATCTTACAGATGGCC[A/G]CTGGACTCTTTTAAG | 23398 |
| rs550657435 | snp | C/G | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65579777 | AATTTTAAAGTAGAA[C/G]TTGATTTTAAGTATT | 23398 |
| rs550753414 | in-del | -/TTTTTTTT | | | upstream-variant-2KB, intron-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65564335 | TTTTTTTTTTTTTTT[-/TTTTTTTT]GAGACGGAGTCTCGC | 23398 |
| rs550854022 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPWD1 | GRCh38.p7 | 5:65582984 | ATTGTTCATAAAATT[C/T]TTACCAGATGAAAAC | 23398 |
| rs550889702 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65562295 | GGCAAGAACGAACAA[C/G]GGAAATTTGTGAGAC | 23398 |
| rs550978681 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65584226 | CAGTCTCACTTTAAG[G/T]GCTCAAAACCCATGT | 23398 |
| rs551024031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | PPWD1 | GRCh38.p7 | 5:65568861 | AGTATATATATACAT[A/G]TTAGCATTGCTGTCA | 23398 |
| rs551024938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65585166 | AGATTTAAGCGCAAG[A/G]AATCTTCTTCTCTCA | 23398 |
| rs551043745 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPWD1 | GRCh38.p7 | 5:65583766 | CTAGCCCGAGCAACA[C/T]GGCAAGACTCTATCT | 23398 |
| rs551046522 | snp | G/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65578727 | ATATGTATATACATA[G/T]ATATATACATATATA | 23398 |
| rs551231921 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPWD1 | GRCh38.p7 | 5:65571360 | AAGATTTAGTTAGTA[A/G]TGAGAGTGTTTTAGG | 23398 |
| rs551286521 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | CENPK, PPWD1 | GRCh38.p7 | 5:65562962 | TGCGTTGGCGCGCGG[G/T]AAGCCGAGAAGAACG | 23398 |
| rs551494469 | snp | C/T | 7.16255e-05 | 0.00598395 | upstream-variant-2KB, intron-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65563518 | AAAGGTAGCTGCAGA[C/T]ATAGTACCGGGACGA | 23398 |
| rs551675898 | snp | C/T | | | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65566457 | GACAAAACATTTCCA[C/T]TTTTACTCATTAGCA | 23398 |
| rs551779375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65569467 | CAGAAAGGAGTTTCA[A/G]AATTTGCAGTGTTCT | 23398 |
| rs551908175 | snp | C/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65571413 | TGTCATAATAAAATA[C/T]TTGATTTAAATATTT | 23398 |
| rs552044726 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPWD1 | GRCh38.p7 | 5:65583451 | CAAAATGTATTGGCT[A/C]TGAAAGTGCTGAGTG | 23398 |
| rs552252365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65580559 | TGCTCTGTTGCCCAG[A/G]CTAGAGTGCAGTGAC | 23398 |
| rs552339462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65575678 | TTTGGAAGGTTCATA[A/G]TATGTTAATACAGTT | 23398 |
| rs552356524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65566373 | ATTAAGATTACAGCA[A/G]TTATATCCCAGTTCC | 23398 |
| rs552933538 | snp | A/G | 6.66822e-05 | 0.00577379 | missense | PPWD1 | GRCh38.p7 | 5:65583069 | CAGAAGATACGAAAA[A/G]TGCAGATTCTGATCG | 23398 |
| rs552987689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65582265 | AGAAGTCCAGAGTTT[C/T]AACAACTGAAAGGTT | 23398 |
| rs553263413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65576785 | ATGTATTCTGCTTCT[A/G]TTTAAATTCTCATTG | 23398 |
| rs553415564 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPWD1 | GRCh38.p7 | 5:65570555 | GTCAGAAAGTTTTGG[A/G]ACTCGCCTTAGTCTG | 23398 |
| rs553444169 | in-del | -/AC | 0.24224 | 0.24988 | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65561600 | TTGTTTAATTAAAAC[-/AC]ACACACACACACACA | 23398 |
| rs553540180 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65563691 | TTTAAGCGTAGTACA[A/G]CGTCTTTTTGATAAT | 23398 |
| rs553552680 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65563130 | CTCCAGGTCGCCTAG[A/G]CGCTGCGCAGGAAGC | 23398 |
| rs553771961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65585258 | GGATGGTCATAAATA[C/T]CAACATCTAGAATCA | 23398 |
| rs553944559 | snp | A/C | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65581890 | ATTTTTCAGATCCAA[A/C]ATGAAATAAAAGTAT | 23398 |
| rs553988605 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65586345 | AAATTATGTGACTAA[G/T]CAGTTTAGAATTGGT | 23398 |
| rs554381543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65572779 | TTCTGTGTAATTCAC[C/T]GGAGTCCTGCCAATT | 23398 |
| rs554469161 | snp | C/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65564763 | CATTCTAAAATCACT[C/G]GAGAATCGGTCTTGT | 23398 |
| rs554480353 | snp | A/C | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65573874 | AGAGTGACTCTAGCC[A/C]TCACTTGTTAGACTG | 23398 |
| rs554498010 | in-del | -/TG | 0.00119737 | 0.0244387 | intron-variant | PPWD1 | GRCh38.p7 | 5:65578780 | ATATATACATATATA[-/TG]TGTGTATATATATAT | 23398 |
| rs554523332 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65566676 | GTTATTTTATTTGGG[A/T]TACATATAATTCTCC | 23398 |
| rs554647125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65575086 | TTTAGTATTTATTAA[C/T]CAGGGTCACTATATA | 23398 |
| rs554704199 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPWD1 | GRCh38.p7 | 5:65582088 | GATGTTAAGGTGATA[A/G]CATCCTAACTTGGTT | 23398 |
| rs554991094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65574685 | AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTCAT | 23398 |
| rs555057384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65583306 | CAACTTAAAATTCCC[A/G]TTACTTTGACTTAAG | 23398 |
| rs555252099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65569052 | ATGATGATAAAAATA[C/T]GTAGAGTTGCTGTAA | 23398 |
| rs555395594 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65576327 | TTCTATTAACCAACC[G/T]GGTTTTGTTTTAAAT | 23398 |
| rs555737384 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | PPWD1 | GRCh38.p7 | 5:65578777 | ATATATATATACATA[C/T]ATATGTGTATATATA | 23398 |
| rs555866845 | in-del | -/AA | 0.498481 | 0.027514 | intron-variant | PPWD1 | GRCh38.p7 | 5:65565808 | GCAAGACTCCGTCTC[-/AA]AAAAAAAAAAAAAAA | 23398 |
| rs556163388 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPWD1 | GRCh38.p7 | 5:65578952 | GAGATGGAGTCTTGT[C/T]CTGTCACCCAGGCTG | 23398 |
| rs556198332 | snp | G/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65578838 | TTTTTAAAAAAAGAG[G/T]TTTTTATATATTTTG | 23398 |
| rs556262640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65579737 | TCCTAAACAACCAGA[A/G]TACCATCTTACATTA | 23398 |
| rs556445439 | snp | A/G | | | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65562703 | TGAAATCCTATACCA[A/G]AGAGAAGAAAGAAGA | 23398 |
| rs556545623 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65566558 | ATAAATGGGGGTTCT[G/T]TTCCTAAAAATGAAG | 23398 |
| rs556762742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65573806 | TTAACTTATGATTCT[A/G]TCTCCAGCAGTGAGA | 23398 |
| rs557060559 | snp | A/G | | | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65566608 | CACAAGCCTGAAACA[A/G]CTCGTCATGTTTAAT | 23398 |
| rs557061655 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65568002 | CAGATGAGTAGGTTC[A/G]TGTAGAAGGATAATA | 23398 |
| rs557204321 | snp | A/G | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65575694 | TATGTTAATACAGTT[A/G]TTGAGATGTGATGCC | 23398 |
| rs557250734 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | PPWD1 | GRCh38.p7 | 5:65580773 | CTGACTCAGCCTCCC[-/A]AAAGTGCTGGAATTA | 23398 |
| rs557370147 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65567375 | ACATACTGGATTTTT[A/T]AATTGTGAATTGAGA | 23398 |
| rs557387570 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65578094 | GATATAGCTAAAATC[A/C/G]TACAGTATGTAGTCT | 23398 |
| rs557455432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65577224 | ACTGGATTTTTCTGT[A/G]GTCTCTTGGTTGTTT | 23398 |
| rs557651619 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65562576 | TGTATTTGATTTTTT[A/T]AAAAAGAGATTAAGA | 23398 |
| rs557829625 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65562486 | GAAGAGATTTACGAC[C/G]AGGATTTTATTAGGT | 23398 |
| rs558001621 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65563105 | GGTCTTACCATCACA[A/G]CGTCACAAACTCCAG | 23398 |
| rs558318553 | snp | A/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65563996 | TAATAAATTTTCGCA[A/T]CTAGGGAAAATGACG | 23398 |
| rs558362426 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65586252 | AGTGAACTCAGTAGA[A/C]GAGCTGCATTATTCT | 23398 |
| rs558452880 | snp | A/C | 1.71569e-05 | 0.00292885 | intron-variant | PPWD1 | GRCh38.p7 | 5:65571821 | TTTTTTTTCCCTCTC[A/C]ATTCTTTACGATTTT | 23398 |
| rs558460646 | snp | A/C | | | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65567338 | TCAGTGCTCTGAAAT[A/C]ATAGACGTTAAAACT | 23398 |
| rs558510925 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65564594 | AAAAGTGCTGGGATT[A/G]CAGGCATGAGCCACG | 23398 |
| rs558588259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65574576 | TCACGCCATTCTCCT[A/G]CCTCAGCCTCCCGAG | 23398 |
| rs558636201 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65572700 | CCTGTCTTCATAAAT[C/G]GTGCCAGTATCCATC | 23398 |
| rs558649027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65574081 | CAGTGACCAATTTGC[A/G]TTGGATTCCCTGCTG | 23398 |
| rs558713492 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65567207 | TTTTTTCTTTTCTTT[C/T]TTTTTAATAGAACAT | 23398 |
| rs558773039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65566612 | AGCCTGAAACAGCTC[A/G]TCATGTTTAATTTAG | 23398 |
| rs558803674 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PPWD1 | GRCh38.p7 | 5:65581482 | TCTCAGCCATGCTGG[A/C]AGCTGATGTGGTAGG | 23398 |
| rs558852980 | snp | C/G | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65584490 | ACAATGCTTTTGTAA[C/G]AAAATGACCTTTCCC | 23398 |
| rs559329499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65581207 | CTTTCAAAATTATTA[C/T]TAAAAATTTATTAGT | 23398 |
| rs559565314 | snp | C/T | 2.35696e-05 | 0.00343282 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65567467 | CAAAATAGTATTTGG[C/T]TTATTTGTTAAAAAT | 23398 |
| rs559594645 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65566363 | CTGAATGATTATTAA[A/G/T]ATTACAGCAGTTATA | 23398 |
| rs559625842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65575435 | TGTAAGACCTTGACC[C/T]TGTGCTTATACCCTA | 23398 |
| rs560175607 | snp | G/T | 1.66524e-05 | 0.00288547 | missense | PPWD1 | GRCh38.p7 | 5:65585057 | GTTCACAGCAGAAAT[G/T]GTTATTATAATGGGC | 23398 |
| rs560311475 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65578384 | TGGATCATATGGTAA[A/C]AGAATGTTTAGTTTT | 23398 |
| rs560426029 | snp | A/G | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65583341 | TTTGAAGAAACGTTT[A/G]ATAAAAAACATCTAT | 23398 |
| rs560561894 | snp | A/G | | | intron-variant, utr-variant-5-prime | PPWD1 | GRCh38.p7 | 5:65568712 | TTTTTAGATCAGTCT[A/G]TTCTTGATGTCTTGA | 23398 |
| rs560562126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65585590 | TGGCAGGTCAGAAAC[A/G]GCAGGATGAAAAGTC | 23398 |
| rs560649040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65578818 | TATGTGTATATATAT[A/G]CTTTTTTTTAAAAAA | 23398 |
| rs560705138 | snp | C/T | 1.65184e-05 | 0.00287384 | synonymous-codon, intron-variant | PPWD1 | GRCh38.p7 | 5:65572118 | TGTGAACTGGGAATA[C/T]AAAACTGACACTGAT | 23398 |
| rs560760804 | in-del | -/TA | 0.00119737 | 0.0244387 | intron-variant | PPWD1 | GRCh38.p7 | 5:65584387 | GAAAGCTTCGTACTC[-/TA]TGAGTGTGATTGTCA | 23398 |
| rs560980882 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65574219 | GACAAATGTGAAGAT[C/G]TGTTTGCCAGCCAAA | 23398 |
| rs560991062 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPWD1 | GRCh38.p7 | 5:65566177 | AAGTTTATCTACATA[C/T]TACAGAAAAACCCAA | 23398 |
| rs561055896 | snp | A/C/G | 3.34601e-05 | 0.00409012 | missense, synonymous-codon | PPWD1 | GRCh38.p7 | 5:65579562 | TCTTCAGAATATTCA[A/C/G]GCTGACCCAACAATA | 23398 |
| rs561373865 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65582389 | TAGGTCAGTTGGGAC[A/T]GTGAAAAAAAATTAA | 23398 |
| rs561623348 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65581872 | ATATGAATTTTGTGT[C/G]CCATTTTTCAGATCC | 23398 |
| rs561645151 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PPWD1 | GRCh38.p7 | 5:65575477 | TCATTTTGATTTTTT[G/T]AGTTTTGTATATAGT | 23398 |
| rs561841164 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime, missense | CENPK, PPWD1 | GRCh38.p7 | 5:65563359 | AGACGTAGAAGGCGC[C/G]GGGACCCGGAGGAAC | 23398 |
| rs562175123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65583482 | TAAACTGTAAAGTGA[C/T]ACACAAATGTGTATC | 23398 |
| rs562177669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65577559 | GAACAGAACTTAATA[C/T]TTTAAGGAGAAAAAA | 23398 |
| rs562199696 | snp | C/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65566086 | CCATGTGACCTAGAA[C/T]GTATTGTGTTCTTAG | 23398 |
| rs562266073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65569332 | AGGGTAATTTTAGCA[A/G]TAAGGAATCCAAAGT | 23398 |
| rs562427839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65578252 | CACGTACTGAAAGAC[A/G]TCTTGGTTGCTTCCA | 23398 |
| rs562441873 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65578829 | ATATACTTTTTTTTA[A/T]AAAAAGAGTTTTTTA | 23398 |
| rs562441907 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPWD1 | GRCh38.p7 | 5:65586532 | GTATATGAATTCACA[A/G]TTTTGAGACAATTTC | 23398 |
| rs562454053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65585777 | AAAGACAGAACATGT[C/T]TATAAATGAGAAGAC | 23398 |
| rs562484069 | snp | A/C | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65577823 | CACATGCATAGCCTC[A/C]CCATTATCAACGTCC | 23398 |
| rs562518183 | snp | A/G | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65582969 | TTCATTAGAAATTCT[A/G]TTGTTCATAAAATTT | 23398 |
| rs562554251 | in-del | -/TTT | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65579788 | GAAGTTGATTTTAAG[-/TTT]TATTTCTGTACTGTT | 23398 |
| rs562578802 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPWD1 | GRCh38.p7 | 5:65579148 | TCTCGAACTCCTGAC[C/T]TCAAGTGATCTGCCT | 23398 |
| rs562702386 | snp | A/C | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65576575 | TGGAGACGGGGTTTC[A/C]CCATGTTGGCCAGGC | 23398 |
| rs562774044 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPWD1 | GRCh38.p7 | 5:65571192 | TTGAACATCAGCACC[A/G]TGGTTAGAATAATAG | 23398 |
| rs562963051 | in-del | -/TCCTCTGAG | 0.00119737 | 0.0244387 | intron-variant | PPWD1 | GRCh38.p7 | 5:65573996 | AAGTGGTTCTCTGAA[-/TCCTCTGAG]TCTGGATTGAACCTT | 23398 |
| rs562986908 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65564894 | CTTAGCTATCATCTT[C/T]TCTGGGAAGCCTGTG | 23398 |
| rs563243626 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | PPWD1 | GRCh38.p7 | 5:65587596 | TGGGAGGTGATAAAT[G/T]GAAATGGACTAAACT | 23398 |
| rs563342508 | snp | A/G | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65570278 | TACTGGAGCTCTGTC[A/G]TATCTAATTACTGGT | 23398 |
| rs563393501 | snp | C/T | 0.0217236 | 0.101931 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65566700 | ATTCTCCCCTCCCCT[C/T]GTTCCCTCCTTCCTT | 23398 |
| rs563535043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65574307 | GGAGAAACATTTATC[A/G]GTAATACTTTCTTTA | 23398 |
| rs563611672 | snp | C/T | | | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65561921 | CTGGCTTTAGCTGTG[C/T]AGATGAAAAAGTCTT | 23398 |
| rs563634511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65583351 | CGTTTGATAAAAAAC[A/G]TCTATTCCTGAGCTT | 23398 |
| rs563638504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65575637 | TGCCCTGATTGTGTA[A/G]AAAAGAATGTAAAGA | 23398 |
| rs563639206 | snp | C/T | | | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65568265 | TGTTTGTTGAGCTTA[C/T]AGTATGTCCCAGGTA | 23398 |
| rs564105938 | snp | C/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65585992 | TTTTTGTGTACTTTC[C/T]GTTAAGGGCTTTATG | 23398 |
| rs564146331 | snp | A/G | 0.00011568 | 0.0076044 | missense, intron-variant, utr-variant-5-prime, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65567570 | CATCCATGTATGAGC[A/G]CAGTTACATGCATAG | 23398 |
| rs564465725 | snp | A/G | | | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65561283 | GCGAAAAAGTCAAAC[A/G]TAAATATTTCTTTAC | 23398 |
| rs564528958 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65583778 | ACACGGCAAGACTCT[A/C]TCTCTTAAAAAAAAT | 23398 |
| rs564568040 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65578285 | TTTTGGCAGTTATGT[A/T]TAAAAGCTGCTATAA | 23398 |
| rs564580538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65577723 | ATTGATTGTTTTTAA[C/T]AGACCTTACTTTTTT | 23398 |
| rs564613375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65584843 | AATATACTACTTACA[C/T]GACCCTCCGTGCTTG | 23398 |
| rs564648227 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | CENPK, PPWD1 | GRCh38.p7 | 5:65562963 | GCGTTGGCGCGCGGG[A/T]AGCCGAGAAGAACGG | 23398 |
| rs564705552 | snp | C/T | 0.000157157 | 0.00886305 | intron-variant | PPWD1 | GRCh38.p7 | 5:65570034 | ATATATTTTAACTTA[C/T]TGAAGTAATTTGTAA | 23398 |
| rs564761176 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | CENPK, PPWD1 | GRCh38.p7 | 5:65563250 | TGACAGAAGACTGCG[C/T]CGCTGCTTTGGGATT | 23398 |
| rs564820233 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65585854 | AATACATCATCCAAA[A/T]TTAAGTGTTAAGGGT | 23398 |
| rs564851759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65579218 | CACCGTGCCTGGCCT[C/T]ATTTCTGTTTTTTAA | 23398 |
| rs564972858 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPWD1 | GRCh38.p7 | 5:65573212 | TTACCTATTGAACTG[A/G]TACTTCAAATTTCAA | 23398 |
| rs565118353 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PPWD1 | GRCh38.p7 | 5:65586644 | GCCATAACACAAAAT[G/T]ATAAAAATTACCTAG | 23398 |
| rs565174031 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65564380 | CCCAGGCTGGAGCGC[A/G]TGCAGTGGCGCTATC | 23398 |
| rs565401132 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65565211 | AGACTGTAAACAAGT[A/C]AGAACCAGAATCACG | 23398 |
| rs565407332 | in-del | -/AC | 0.031825 | 0.122064 | intron-variant | PPWD1 | GRCh38.p7 | 5:65578795 | TGTGTATATATATAT[-/AC]ACATATATATGTGTA | 23398 |
| rs565593291 | snp | C/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65584430 | TAAATTTAGATGTCA[C/T]TTCTATGATTAAGGT | 23398 |
| rs565660875 | snp | A/G | | | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65562335 | AGTAGTCTGATGAGA[A/G]CAGAGGGCAGAGAAG | 23398 |
| rs565687353 | snp | A/G | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65586900 | AAACTATTTCAAACT[A/G]CCTCTGAATAAACTG | 23398 |
| rs565793608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65565669 | AAAAATTAGCCGGGC[A/G]TGGTGGCGCACACCT | 23398 |
| rs566029569 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPWD1 | GRCh38.p7 | 5:65581509 | TAGGATCTCTTGAGC[C/T]AACGAATTCAAGGTT | 23398 |
| rs566042641 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PPWD1 | GRCh38.p7 | 5:65582043 | AAATAGTACAACAGA[C/G]ATGCCATTCCTTTGA | 23398 |
| rs566049674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65567754 | TGAAATAAAGGCCTA[C/T]ATGTTCTTTCCTATA | 23398 |
| rs566152429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65582570 | TCACAACTACCTTCA[C/T]TGCAAGGTATGTACT | 23398 |
| rs566310669 | snp | C/G/T | 6.65973e-05 | 0.00577019 | missense | PPWD1 | GRCh38.p7 | 5:65579553 | AAATCCTGTTCTTCA[C/G/T]AATATTCAAGCTGAC | 23398 |
| rs566501437 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65561405 | ATTATCTGGCTTGGC[G/T]ATTTAATGTGGCAGT | 23398 |
| rs566514474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65583788 | ACTCTATCTCTTAAA[A/G]AAAATTTTTTTTTAT | 23398 |
| rs566751916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65577826 | ATGCATAGCCTCCCC[A/G]TTATCAACGTCCCCC | 23398 |
| rs566838789 | snp | A/G | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65574154 | TTGATTTGGTGGCAC[A/G]TGGTAATAAATGAGT | 23398 |
| rs566870661 | snp | G/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65577232 | TTTCTGTGGTCTCTT[G/T]GTTGTTTATAATCTT | 23398 |
| rs566989049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65570096 | AAATAGTATATTACC[A/G]TATCTTTAAATAAAA | 23398 |
| rs566989352 | snp | A/G | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65562446 | CCTTCCCTGTACGTG[A/G]TGCCTATCTCAAGGC | 23398 |
| rs567014120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65571757 | AATCACCAGCCAAGA[C/T]ATTTTTGGTAGTGGG | 23398 |
| rs567070064 | snp | C/T | | | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65566847 | TTGCTAGTAAAATTG[C/T]TCATACCTCATATAA | 23398 |
| rs567153426 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65563695 | AGCGTAGTACAACGT[A/C]TTTTTGATAATATCT | 23398 |
| rs567243284 | snp | A/G/T | 8.59179e-05 | 0.00655381 | intron-variant | PPWD1 | GRCh38.p7 | 5:65585959 | AAGCGTACATATATC[A/G/T]AAAAGGACAATGTAA | 23398 |
| rs567378337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65572470 | AGTCTCTTCTCTAGG[A/G]GTTTATGATGTGCGT | 23398 |
| rs567648083 | snp | A/C | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65572715 | GGTGCCAGTATCCAT[A/C]TAGTTGCTCAAACCA | 23398 |
| rs567820327 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65580622 | GGGTTCCAGCAATTC[G/T]CCTGCCTCAGTCTCC | 23398 |
| rs567874837 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65581305 | AAAAGATAATTCTTG[G/T]CCAGGAATGGTGGCT | 23398 |
| rs567932379 | in-del | -/TT | 0.00279162 | 0.0372561 | intron-variant | PPWD1 | GRCh38.p7 | 5:65581805 | TTGTTACGAATTTTC[-/TT]TGAGTCTTACTAGTA | 23398 |
| rs567956702 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPWD1 | GRCh38.p7 | 5:65573779 | AGTAGACTAAGCCCT[A/G]TGTGATCTGTTTTAA | 23398 |
| rs568411541 | snp | C/T | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65586267 | AGAGCTGCATTATTC[C/T]GTATTTTCTGCATTA | 23398 |
| rs568434083 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65561567 | CCAGCCTCTAGACCT[A/C/G]TGAGAAATAAATTTC | 23398 |
| rs568455402 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | PPWD1 | GRCh38.p7 | 5:65567887 | CCCTGAAGAAGAGGG[C/T]ACATTAGTTAAGATA | 23398 |
| rs568469459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65575947 | ACGTAACCTTGCTCA[A/G]GGACCTCATAGTCTA | 23398 |
| rs568823396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65578450 | CTTTTTGCATTCCCA[C/T]CAGCAATGAATGAGT | 23398 |
| rs569057927 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | PPWD1 | GRCh38.p7 | 5:65578733 | ATATACATATATATA[C/T]ACATATATATATACA | 23398 |
| rs569532123 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | PPWD1 | GRCh38.p7 | 5:65580498 | TCCTAACTCATACTT[-/C]CAAGTTTCAGTTTGG | 23398 |
| rs569552981 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65587040 | GATGCAGATATTTAA[A/T]TAAACATTATACTAT | 23398 |
| rs569651032 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | PPWD1 | GRCh38.p7 | 5:65573470 | GCTAATATATATATA[G/T]ATATATTTTTTTTTT | 23398 |
| rs569732647 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CENPK, PPWD1 | GRCh38.p7 | 5:65564478 | GGGCTACAGGCGCAC[A/G]CCCAGCTAATTTTTG | 23398 |
| rs569887601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65574532 | GTAGTGGCTCAATCG[C/T]GGCTCACTGCAAGCT | 23398 |
| rs570169028 | snp | A/G | | | intron-variant | PPWD1 | GRCh38.p7 | 5:65571436 | AAATATTTCAAGAAA[A/G]GATTTATAAAATACA | 23398 |
| rs570337113 | in-del | -/AAC | 0.0182019 | 0.0936463 | intron-variant | PPWD1 | GRCh38.p7 | 5:65586363 | GTTTAGAATTGGTAA[-/AAC]AATACTGCCACTGTA | 23398 |
| rs570749139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65576059 | GCTGAAAGTGTAAAA[C/T]ACAAGATTTCAAAGA | 23398 |
| rs570763596 | snp | A/G | 0.000102662 | 0.00716384 | missense | PPWD1 | GRCh38.p7 | 5:65583048 | TTGAGTTTACCAAAC[A/G]AGAACCAGAAGATAC | 23398 |
| rs570808789 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65561719 | CCCCAGTTAGGACTA[C/G]AATACTTAATCATTT | 23398 |
| rs570870496 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | PPWD1 | GRCh38.p7 | 5:65568865 | TATATATACATATTA[C/G]CATTGCTGTCACTCT | 23398 |
| rs570885769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65576668 | GCATAAGCCACCATG[C/T]CCAGCCTGAAATACT | 23398 |
| rs570921954 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PPWD1 | GRCh38.p7 | 5:65569440 | TAGTACAGCTGTAAC[G/T]GTTTTGACATCCAGA | 23398 |
| rs571002547 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPWD1 | GRCh38.p7 | 5:65578471 | ATGAATGAGTGTTCC[C/T]GTCACTCCACATCTG | 23398 |
| rs571061440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CENPK, PPWD1 | GRCh38.p7 | 5:65562302 | ACGAACAAGGGAAAT[C/T]TGTGAGACACAAAAG | 23398 |
| rs571134921 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPWD1 | GRCh38.p7 | 5:65570485 | CATGTCTTTTTTAAG[A/C]TAACATAGAATTTAT | 23398 |
| rs571222314 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPWD1 | GRCh38.p7 | 5:65571398 | TTTTCTTTGACGTAT[C/T]GTCATAATAAAATAT | 23398 |
| rs571776538 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPWD1 | GRCh38.p7 | 5:65587160 | ATGCTAAAGGGGAGC[A/G]TAAACTTAAATTCTC | 23398 |
| rs571866257 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PPWD1 | GRCh38.p7 | 5:65584852 | CTTACATGACCCTCC[A/G]TGCTTGTCCTGAGAT | 23398 |
| rs572158003 | snp | A/G | 6.62669e-05 | 0.00575578 | synonymous-codon | PPWD1 | GRCh38.p7 | 5:65587363 | AGATAAGCCCTATGA[A/G]GATGTCAGCATCATA | 23398 |