SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs744266 | snp | A/G | 0.44252 | 0.159487 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107685408 | TTAGGGATGTAATGA[A/G]ATGTAATGGTGGGAT | 11137 |
rs744267 | snp | C/T | 0.355311 | 0.226737 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107685669 | GCCGGGCGAGGAATC[C/T]ACGTGGGCTGGTCTG | 11137 |
rs1106621 | snp | A/G | 0.00557542 | 0.0525036 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107684331 | ttattggccaaagca[A/G]acctacaactaccca | 11137 |
rs1802936 | snp | C/T | | | missense | PWP1 | GRCh38.p7 | 12:107697527 | GGGACCTTGATATAG[C/T]GGACTCTTTAGAGCC | 11137 |
rs1802937 | snp | C/T | 0.0333695 | 0.124785 | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712281 | AAGTTGGCCTAAAAA[C/T]GTTCCATGCGTGGCA | 11137 |
rs1802938 | snp | A/T | | | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712383 | ACAAATATCCGGTCT[A/T]TGTGCTTGCTCTTCA | 11137 |
rs2241218 | snp | A/G | 0.42803 | 0.175514 | intron-variant | PWP1 | GRCh38.p7 | 12:107686200 | TGGGAGTGGGGTTGG[A/G]CTTGAGGGTGGGAAC | 11137 |
rs2287214 | snp | C/T | 0.345704 | 0.230956 | intron-variant | PWP1 | GRCh38.p7 | 12:107696741 | CAAACAATAAAGTGA[C/T]GGTGTGTTAAGAACT | 11137 |
rs2287215 | snp | G/T | 0.371349 | 0.218574 | intron-variant | PWP1 | GRCh38.p7 | 12:107693119 | CACTTAGAAAATCTT[G/T]TAATAAGGGATTTAT | 11137 |
rs2287216 | snp | A/G | 0.446818 | 0.154169 | intron-variant | PWP1 | GRCh38.p7 | 12:107692920 | TAAGAGCATAATTAG[A/G]AAAAAGATGTAAATA | 11137 |
rs2287217 | snp | C/T | 0.34659 | 0.230587 | intron-variant | PWP1 | GRCh38.p7 | 12:107704810 | AGATAATTCTCTCTA[C/T]TATGGAATTTAAAAA | 11137 |
rs2302737 | snp | A/G | 0.345482 | 0.231048 | intron-variant | PWP1 | GRCh38.p7 | 12:107710630 | AAGGCTGAGGACCAA[A/G]GATTGCTTGAGGCCA | 11137 |
rs2374711 | snp | C/T | 0.416871 | 0.186156 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107683834 | gacggggtttcacta[C/T]gttggccaggcttgt | 11137 |
rs3741786 | snp | C/T | 0.141934 | 0.225437 | intron-variant | PWP1 | GRCh38.p7 | 12:107703113 | CCAAACGTTTATATA[C/T]GGCTTTGAAAATAAT | 11137 |
rs3741787 | snp | G/T | 0.141596 | 0.225274 | intron-variant | PWP1 | GRCh38.p7 | 12:107703348 | TGTGTTATTCCCCAG[G/T]AATCTAATGCAGATT | 11137 |
rs3782527 | snp | C/T | 0.4628 | 0.13121 | intron-variant | PWP1 | GRCh38.p7 | 12:107708145 | CTCTCACTCTTCAGG[C/T]ACGCAACTTCCAGAG | 11137 |
rs3825256 | snp | G/T | 0.480853 | 0.0959518 | intron-variant | PWP1 | GRCh38.p7 | 12:107691793 | GATGTTCATTCCTCC[G/T]TTTTCCTCATTCGCT | 11137 |
rs3825257 | snp | C/T | 0.4628 | 0.13121 | intron-variant | PWP1 | GRCh38.p7 | 12:107708585 | TCTTCCCTCTCTGAC[C/T]CACTTCTGTGGATGC | 11137 |
rs4964610 | snp | A/G | 0.471292 | 0.116318 | intron-variant | PWP1 | GRCh38.p7 | 12:107705149 | CTAACCTGTTAATTT[A/G]TAGCACTATCTCCCA | 11137 |
rs4964611 | snp | A/G | 0.33693 | 0.2344 | intron-variant | PWP1 | GRCh38.p7 | 12:107705264 | TCCACTGACATTTCA[A/G]TACATGTAAAAAGAA | 11137 |
rs5800759 | snp | C/G/T | 0.00597247 | 0.0543191 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107684365 | TCAAGTTGGTGGGGG[C/G/T]GGGGGGGGGTGCTTT | 11137 |
rs5800760 | in-del | -/T/TT | 0.5 | 0 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107685359 | CTCACTTTTTTTTTT[-/T/TT]GGTGCTAAATGTTTT | 11137 |
rs6539358 | snp | G/T | 0.351635 | 0.228408 | intron-variant | PWP1 | GRCh38.p7 | 12:107711200 | ctgcagcaggaacat[G/T]cccttaagacacaga | 11137 |
rs6539359 | snp | A/G | 0.425277 | 0.178263 | intron-variant | PWP1 | GRCh38.p7 | 12:107711358 | ttatgaacatgttac[A/G]gtgctgaagagattt | 11137 |
rs7307356 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | PWP1 | GRCh38.p7 | 12:107688263 | TTTCAGGTAGCGAGA[A/G]ATCTTATTTGTAAGA | 11137 |
rs7310670 | snp | C/T | 0.164546 | 0.234942 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107685533 | CAAGCAAAATAAAGA[C/T]TGGTGAAACTTTGCT | 11137 |
rs7310699 | snp | C/T | 0.0134861 | 0.0810011 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107685619 | CATCGTCACATGCAG[C/T]CCTGAAAAGCCTTTT | 11137 |
rs7398764 | snp | A/G | 0.472335 | 0.114312 | intron-variant | PWP1 | GRCh38.p7 | 12:107706641 | agttttcccagcacc[A/G]tttattaaataggga | 11137 |
rs7398797 | snp | A/G | 0.476401 | 0.106032 | intron-variant | PWP1 | GRCh38.p7 | 12:107707008 | tatggctattttcac[A/G]atattgattcttcct | 11137 |
rs7398802 | snp | C/T | 0.473266 | 0.112482 | intron-variant | PWP1 | GRCh38.p7 | 12:107706976 | atggcattgaatcta[C/T]aaattaccttgggca | 11137 |
rs7959279 | snp | C/G | 0.143284 | 0.226079 | intron-variant | PWP1 | GRCh38.p7 | 12:107697876 | TAGATGAAGGACTTT[C/G]GGATTATGAGCCTCC | 11137 |
rs7965275 | snp | A/G | 0.353154 | 0.227726 | intron-variant | PWP1 | GRCh38.p7 | 12:107711609 | GGATCCTGGCTGCTT[A/G]TTTATTACTTTGAGG | 11137 |
rs7970554 | snp | A/G | 0.474903 | 0.109173 | intron-variant | PWP1 | GRCh38.p7 | 12:107700450 | gacttacttctttgc[A/G]actggcttatttgac | 11137 |
rs7971097 | snp | A/G | 0.143622 | 0.226238 | intron-variant | PWP1 | GRCh38.p7 | 12:107700930 | gtaagatgggggtct[A/G]tgttgctaaagctgg | 11137 |
rs7974456 | snp | A/T | 0.471483 | 0.115954 | intron-variant | PWP1 | GRCh38.p7 | 12:107701339 | AATTTTTGGAGTTAA[A/T]ACTAACTCCTACTAC | 11137 |
rs7980305 | snp | C/T | 0.417034 | 0.18601 | intron-variant | PWP1 | GRCh38.p7 | 12:107704262 | TTGCTTCCCCTAACA[C/T]GATAAACTGCTTATG | 11137 |
rs9634190 | snp | A/G | 0.345704 | 0.230956 | intron-variant | PWP1 | GRCh38.p7 | 12:107704193 | TCTTATCCTCTTGAA[A/G]CATGATATGTTTACA | 11137 |
rs10655986 | in-del | -/T/TT | 0.660493 | 0.0452146 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107685349 | ATGTTTTTTTCTCAC[-/T/TT]TTTTTTTTTTGGTGC | 11137 |
rs10746092 | snp | G/T | 0.495708 | 0.0461266 | intron-variant | PWP1 | GRCh38.p7 | 12:107692468 | TTTATTTCCAGGTCC[G/T]CAAGGCTGCCTCTCC | 11137 |
rs10778567 | snp | A/G | 0.435694 | 0.167385 | intron-variant | PWP1 | GRCh38.p7 | 12:107692574 | TAATTCCCTGATACA[A/G]TTCTTTCATTGGAAG | 11137 |
rs10778568 | snp | A/G | 0.495135 | 0.0490805 | intron-variant | PWP1 | GRCh38.p7 | 12:107694019 | TCAAAGCCAGAAGCG[A/G]ATGCTTTGCAGTAAT | 11137 |
rs10778569 | snp | A/G | 0.471673 | 0.115589 | intron-variant | PWP1 | GRCh38.p7 | 12:107694127 | TTGCCTCACTTTGGT[A/G]TTTTTAATGTAAAAT | 11137 |
rs10861764 | snp | C/T | 0.352938 | 0.227824 | intron-variant | PWP1 | GRCh38.p7 | 12:107689876 | ACCTATATTGCTCTT[C/T]TGGGGAAAGTAGGTA | 11137 |
rs10861765 | snp | A/T | 0.470327 | 0.118136 | intron-variant | PWP1 | GRCh38.p7 | 12:107689882 | ATTGCTCTTCTGGGG[A/T]AAGTAGGTATAACGA | 11137 |
rs10861766 | snp | G/T | 0.472147 | 0.114677 | intron-variant | PWP1 | GRCh38.p7 | 12:107698738 | GCTGGGACTATAGGC[G/T]TATGCTGCCATGCCT | 11137 |
rs10861767 | snp | G/T | 0.440195 | 0.162252 | intron-variant | PWP1 | GRCh38.p7 | 12:107700241 | TAAGTGTGCAGTTCA[G/T]TGGCTTTCAGTACAT | 11137 |
rs10861768 | snp | C/T | 0.3512 | 0.228601 | intron-variant | PWP1 | GRCh38.p7 | 12:107700561 | GTAATGTATGTTACC[C/T]GTTCATTTACGTGTG | 11137 |
rs11113439 | snp | C/T | 0.354665 | 0.227036 | intron-variant | PWP1 | GRCh38.p7 | 12:107687402 | ATTGAAAATCTCACA[C/T]TTGGGGAGGTTCAAA | 11137 |
rs11113440 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107688061 | AAAAAAAAAAAAAAA[A/G]AACAGAGGACTCATG | 11137 |
rs11113441 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107688130 | GGGAGAGGTGCCCTA[A/G]ACAGAGTCAGAGATG | 11137 |
rs11113443 | snp | C/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107693411 | aactcctgggctgac[C/G]taatcctgatttggc | 11137 |
rs11113445 | snp | A/G | 0.344592 | 0.231414 | intron-variant | PWP1 | GRCh38.p7 | 12:107694905 | AATAACTTCAAATTT[A/G]TATTCTAAAACTGAT | 11137 |
rs11113446 | snp | C/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107695120 | aaaaaaaaaaaatca[C/G]ccaggcgtggtggcg | 11137 |
rs11113447 | snp | A/G | 0.345704 | 0.230956 | intron-variant | PWP1 | GRCh38.p7 | 12:107705772 | TTAATCCAGTCTATC[A/G]TTGATGGACATCTGG | 11137 |
rs11113448 | snp | G/T | 0.354881 | 0.226936 | intron-variant | PWP1 | GRCh38.p7 | 12:107707352 | TGCAAACAGGGACAA[G/T]TTGACTTCCTCTTTT | 11137 |
rs11113449 | snp | A/T | 0.5 | 0 | intron-variant | PWP1 | GRCh38.p7 | 12:107709528 | TTTTTTTTTTTTTTT[A/T]AAACCCTGAAATCAA | 11137 |
rs11113450 | snp | A/G | 0.345482 | 0.231048 | intron-variant | PWP1 | GRCh38.p7 | 12:107710060 | ACTGGCATCATTGTT[A/G]TTGTTTAAAAGGACA | 11137 |
rs11113451 | snp | C/T | 0.351418 | 0.228505 | intron-variant | PWP1 | GRCh38.p7 | 12:107710153 | GATAACGAAGATGAG[C/T]GGCCTGAGTGGTCAG | 11137 |
rs11350649 | in-del | -/C | 0.355311 | 0.226737 | intron-variant | PWP1 | GRCh38.p7 | 12:107688290 | AAGAATCTATAAAAT[-/C]TATATTTTTTAATAT | 11137 |
rs11417451 | in-del | -/T | | | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107685344 | GCTAAATGTTTTTTT[-/T]CTCACTTTTTTTTTT | 11137 |
rs11547907 | snp | C/G | 0.0758322 | 0.179348 | missense | PWP1 | GRCh38.p7 | 12:107702992 | GTGGGATATGTCCTT[C/G]GGGAAACCAGCAGCT | 11137 |
rs11547909 | snp | A/G | 0.00771695 | 0.0616354 | missense | PWP1 | GRCh38.p7 | 12:107712116 | TGTATTTTAGTAAAT[A/G]AAGCATTTGGAAGAC | 11137 |
rs11831259 | snp | A/G | 0.11228 | 0.208646 | intron-variant | PWP1 | GRCh38.p7 | 12:107699238 | cactctagccagggc[A/G]acagacaaagactcc | 11137 |
rs11831458 | snp | C/T | 0.113334 | 0.209338 | intron-variant | PWP1 | GRCh38.p7 | 12:107687101 | GTTGATTTGAATGTA[C/T]TTGACCAAGATAATG | 11137 |
rs12227529 | snp | C/T | 0.351418 | 0.228505 | intron-variant | PWP1 | GRCh38.p7 | 12:107701203 | acaatcactgctcac[C/T]gtagtcttgaccttc | 11137 |
rs12227720 | snp | A/C | 0.34526 | 0.23114 | intron-variant | PWP1 | GRCh38.p7 | 12:107698939 | GGGAGACAAGGTTTT[A/C]TTTATTTTATTCTTC | 11137 |
rs12227989 | snp | C/T | 0.360842 | 0.224085 | intron-variant | PWP1 | GRCh38.p7 | 12:107702755 | ttccacttatttaga[C/T]actcttgtttccttt | 11137 |
rs12230701 | snp | C/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107699113 | aaaatataaaaatta[C/G]ctgggcatggtggca | 11137 |
rs12230726 | snp | C/T | 0.351635 | 0.228408 | intron-variant | PWP1 | GRCh38.p7 | 12:107690341 | actatgatcacactg[C/T]attccatcctggatg | 11137 |
rs12422550 | snp | A/G | 0.0103295 | 0.0711199 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107684631 | GGGAGATTGCCAAGC[A/G]CATTAGGCTGAGTAG | 11137 |
rs12423629 | snp | C/T | 0.163564 | 0.234582 | intron-variant | PWP1 | GRCh38.p7 | 12:107687440 | gatgtttatgtccca[C/T]tcccaagtattgtgt | 11137 |
rs12423668 | snp | C/T | 0.441977 | 0.16014 | intron-variant | PWP1 | GRCh38.p7 | 12:107687840 | AGTTCCAGACCAGCC[C/T]GGCCAACATGGTGAA | 11137 |
rs12423701 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PWP1 | GRCh38.p7 | 12:107703166 | TTCACATGTTATCTC[G/T]TAGGATTTTCACAAA | 11137 |
rs12424295 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PWP1 | GRCh38.p7 | 12:107689164 | TCACAATAcagtagt[C/T]cccccttatccacgg | 11137 |
rs12426279 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PWP1 | GRCh38.p7 | 12:107687983 | ttgcagtgagccgag[A/G]tggcgccattgctct | 11137 |
rs12426896 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PWP1 | GRCh38.p7 | 12:107701936 | gcctgcctctgcctt[A/G]caaagtgctgggatt | 11137 |
rs12580485 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107690706 | gacctcatgatccgc[C/T]tgcctcggcctGAAA | 11137 |
rs17552177 | snp | C/T | 0.141258 | 0.225111 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107684886 | GCCAGTTTATCCTTG[C/T]CACTGTTTCCCCATA | 11137 |
rs17849519 | snp | C/G | | | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107693089 | CCAGTGCAATTTAGA[C/G]GTGCATGGTAAGTGA | 11137 |
rs17856055 | snp | C/T | | | missense | PWP1 | GRCh38.p7 | 12:107710456 | CCATTTATTTATGCC[C/T]TTGGAGGTCAAAAAG | 11137 |
rs17856056 | snp | C/G | | | missense | PWP1 | GRCh38.p7 | 12:107710459 | TTTATTTATGCCTTT[C/G]GAGGTCAAAAAGAAG | 11137 |
rs28420520 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107690510 | GCTCTGTTGCCCAGG[C/T]TAGAGTGCTGTAGTG | 11137 |
rs28648646 | snp | G/T | 0.20764 | 0.246385 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107685337 | TAATTGGTGCTAAAT[G/T]TTTTTTTCTCACTTT | 11137 |
rs28821814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107700411 | TGAATTTGACTAAGC[A/G]TCTCATATGAATGGA | 11137 |
rs33930962 | in-del | -/G/T | | | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107684372 | GTGGGGGCGGGGGGG[-/G/T]GGTGCTTTGATGGAG | 11137 |
rs34017446 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | PWP1 | GRCh38.p7 | 12:107695720 | AAAAATATTAAGAGT[A/G]ATTTTTGATAAGCAT | 11137 |
rs34183903 | in-del | -/C | | | intron-variant | PWP1 | GRCh38.p7 | 12:107702137 | ATTGCTGTAGATTTT[-/C]CAGTAAGTTTTGATG | 11137 |
rs34233479 | in-del | -/A | | | intron-variant | PWP1 | GRCh38.p7 | 12:107695713 | TTTTTTAAAAATATT[-/A]AAGAGTAATTTTTGA | 11137 |
rs34825894 | in-del | -/A | | | intron-variant | PWP1 | GRCh38.p7 | 12:107689456 | CTTGGAGATAATTAG[-/A]AAAAGAGGCCAGGTG | 11137 |
rs35013338 | in-del | -/C | 0.00636936 | 0.0560724 | intron-variant | PWP1 | GRCh38.p7 | 12:107698562 | AGTTTCTTCCCTGTT[-/C]CTTGTAATGAAATTT | 11137 |
rs35283149 | in-del | -/C | | | intron-variant | PWP1 | GRCh38.p7 | 12:107712070 | ATTCTGACTTAATTT[-/C]CCTGATCTGTTAGTT | 11137 |
rs35371581 | in-del | -/A | 0.498957 | 0.0228094 | intron-variant | PWP1 | GRCh38.p7 | 12:107710553 | TCCCCCTGCCCCTGT[-/A]AAAAAAAAAAAAAAA | 11137 |
rs35612314 | snp | C/T | 0.34303 | 0.232046 | intron-variant | PWP1 | GRCh38.p7 | 12:107699819 | AATTATGGCAAAATA[C/T]ATATAACATAAAAGT | 11137 |
rs35778319 | in-del | -/T | | | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712532 | TAGTAATTTATAGAA[-/T]TTTTAAAGCGTAAAA | 11137 |
rs36074047 | in-del | -/C | 0.356169 | 0.226336 | intron-variant | PWP1 | GRCh38.p7 | 12:107700897 | TTTTAATTTGCATTT[-/C]CCCCCCCTTTTTTTA | 11137 |
rs55954801 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107687997 | GATGGCGCCATTGCT[C/T]TTCAGCCTGGGCAAC | 11137 |
rs56255249 | in-del | -/AAAAAAAAA | | | intron-variant | PWP1 | GRCh38.p7 | 12:107688060 | AAAAAAAAAAAAAAA[-/AAAAAAAAA]GAACAGAGGACTCAT | 11137 |
rs56314609 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107687995 | GAGATGGCGCCATTG[C/T]TCTTCAGCCTGGGCA | 11137 |
rs57219111 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PWP1 | GRCh38.p7 | 12:107701227 | GACCTTCTGGGGCTC[A/G]GGTGATCCTCCCACC | 11137 |
rs57366203 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107687732 | GACCATGCCACATCT[C/T]TTAAAAATTAAAATT | 11137 |
rs58011446 | in-del | -/A | 0 | 0 | intron-variant | PWP1 | GRCh38.p7 | 12:107688060 | AAAAAAAAAAAAAAA[-/A]GAACAGAGGACTCAT | 11137 |
rs58306934 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107687730 | GTGACCATGCCACAT[C/T]TCTTAAAAATTAAAA | 11137 |
rs58377157 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PWP1 | GRCh38.p7 | 12:107694017 | TATCAAAGCCAGAAG[C/T]GGATGCTTTGCAGTA | 11137 |
rs58496865 | snp | G/T | 0.112631 | 0.208878 | intron-variant | PWP1 | GRCh38.p7 | 12:107701288 | ATGAGCCACCAAGCC[G/T]GGCCTCCCTTTGCCT | 11137 |
rs59081821 | snp | A/G | 0.494936 | 0.050064 | intron-variant | PWP1 | GRCh38.p7 | 12:107695986 | CCACAAGATGGCACT[A/G]TATTAGACATGCAGA | 11137 |
rs60944319 | snp | A/C | 0.113334 | 0.209338 | intron-variant | PWP1 | GRCh38.p7 | 12:107705885 | TGTCTTTATAGCAGC[A/C]TGATTTATAATCCTT | 11137 |
rs61728433 | in-del | -/AAAAAAAAAAAAAAAAAAAA | 0.0633504 | 0.166319 | intron-variant | PWP1 | GRCh38.p7 | 12:107686970 | GTGAGACTCCGTCTC[-/AAAAAAAAAAAAAAAAAAAA]AAAAAAAAAAATAGA | 11137 |
rs61730727 | snp | C/T | 0.0354603 | 0.128346 | synonymous-codon | PWP1 | GRCh38.p7 | 12:107702941 | CTTTCTCAGAAATGT[C/T]TTAGCAAGTGCATCA | 11137 |
rs61938560 | snp | A/C | 0.5 | 0 | intron-variant | PWP1 | GRCh38.p7 | 12:107694368 | TAGGAAACACAGTTG[A/C]ACAGCTTGAAAAAAT | 11137 |
rs61938562 | snp | C/T | 0.364609 | 0.222182 | intron-variant | PWP1 | GRCh38.p7 | 12:107696221 | TATTTTGAGTAGAGA[C/T]GAGGTTTCATTGTGT | 11137 |
rs61938563 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PWP1 | GRCh38.p7 | 12:107703589 | CAGAGGGACGCATTT[A/G]TAGAAATACTGTCAA | 11137 |
rs61938564 | snp | A/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107705390 | TTTTTTTTTTTTTAA[A/T]TTTAAGTTCTAGGAT | 11137 |
rs61938565 | snp | C/T | 0.353803 | 0.227431 | intron-variant | PWP1 | GRCh38.p7 | 12:107709577 | TGAACCTCAGGGCAC[C/T]GTAGCTATTAGGGTC | 11137 |
rs61938566 | snp | C/T | 0.179105 | 0.239737 | intron-variant | PWP1 | GRCh38.p7 | 12:107711566 | CAAAATCCAACTTTC[C/T]GGAAGGGGCCACTCC | 11137 |
rs61938567 | snp | A/G | | | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712475 | AAAAAGTAATTCCTT[A/G]AACATACCATCTGTC | 11137 |
rs67004886 | in-del | -/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107687000 | CAGGGTCTTTTTCTA[-/T]TTTTTTTTTTTTTTT | 11137 |
rs67446565 | snp | C/G | 0.209388 | 0.246679 | intron-variant | PWP1 | GRCh38.p7 | 12:107704288 | TTATGGAGAGTAAGT[C/G]TGCCTAAGACATGAG | 11137 |
rs71442063 | in-del | -/T | 0.350327 | 0.228986 | intron-variant | PWP1 | GRCh38.p7 | 12:107702243 | GAATCAGCTTGTCAC[-/T]CTTTTTTTTTAAGTC | 11137 |
rs71959769 | in-del | -/TT | | | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107685358 | TCTCACTTTTTTTTT[-/TT]TGGTGCTAAATGTTT | 11137 |
rs72430499 | in-del | -/T/TT | | | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107685350 | TGTTTTTTTCTCACT[-/T/TT]TTTTTTTTTGGTGCT | 11137 |
rs73187393 | snp | C/T | 0.142947 | 0.22592 | intron-variant | PWP1 | GRCh38.p7 | 12:107698418 | ATAGTCCTAGCACTT[C/T]GGGAGGCCAAGGTGG | 11137 |
rs73187394 | snp | C/T | 0.142947 | 0.22592 | intron-variant | PWP1 | GRCh38.p7 | 12:107702177 | ATGAACTTGCCAACT[C/T]TGTTCTTTTTTTCAG | 11137 |
rs73187397 | snp | C/T | 0.141596 | 0.225274 | intron-variant | PWP1 | GRCh38.p7 | 12:107702780 | TCCTTTCATAATCTT[C/T]GGTAGTTTTCATTAT | 11137 |
rs73187399 | snp | C/T | 0.143284 | 0.226079 | intron-variant | PWP1 | GRCh38.p7 | 12:107703602 | TTATAGAAATACTGT[C/T]AAATAGATTCTTACC | 11137 |
rs73398379 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | PWP1 | GRCh38.p7 | 12:107689952 | TTGGAATGTGCTACC[C/T]TAGGTGGCACTAACT | 11137 |
rs73398381 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PWP1 | GRCh38.p7 | 12:107700025 | GAAAGGGCATGTGCA[A/G]AGGAACTCTCCTTTA | 11137 |
rs73398383 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | PWP1 | GRCh38.p7 | 12:107701534 | GGTCATGAAGGTTTA[C/T]ATGTATGTTTTCTTC | 11137 |
rs74340456 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | PWP1 | GRCh38.p7 | 12:107701418 | TCACTTTCTTGGTGC[C/T]ATCATTTGCAGCACA | 11137 |
rs74468350 | snp | A/G | 0 | 0 | intron-variant | PWP1 | GRCh38.p7 | 12:107689014 | GGATCTAAAAAAAAA[A/G]GTACTGTGTATTTTA | 11137 |
rs74478045 | snp | A/T | 0.0558544 | 0.157504 | intron-variant | PWP1 | GRCh38.p7 | 12:107690859 | TATAATACAACATTT[A/T]AAAAAAAATCAGACA | 11137 |
rs74573164 | snp | C/G | 0.113685 | 0.209567 | intron-variant | PWP1 | GRCh38.p7 | 12:107693900 | AGATATTTCCCCTTT[C/G]CAAAACATTTTATTT | 11137 |
rs74612962 | snp | A/C | 0.0663309 | 0.169604 | intron-variant | PWP1 | GRCh38.p7 | 12:107699603 | CTGTTTCTTTGCATC[A/C]TCCAGGTCACCTGCC | 11137 |
rs74918182 | snp | A/G | 0.0367279 | 0.130442 | missense | PWP1 | GRCh38.p7 | 12:107708980 | CGTTCAGATAAGCCA[A/G]TTTTTACACTTAATG | 11137 |
rs74977517 | snp | C/G | 0.0866379 | 0.189243 | intron-variant | PWP1 | GRCh38.p7 | 12:107710540 | TTCTCTGCACACCTC[C/G]CCCTGCCCCTGTAAA | 11137 |
rs75054122 | snp | C/T | 0.0182019 | 0.0936463 | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712480 | GTAATTCCTTAAACA[C/T]ACCATCTGTCACAGT | 11137 |
rs75330461 | snp | A/C | 0.113334 | 0.209338 | intron-variant | PWP1 | GRCh38.p7 | 12:107710286 | GGCTTGAAAGTGAGA[A/C]TCATAAGTTGGTTTT | 11137 |
rs75897229 | snp | A/C | 0.5 | 0 | intron-variant | PWP1 | GRCh38.p7 | 12:107695265 | AGCAAGACTCCATCT[A/C]AAAAAAAAAAAAGTT | 11137 |
rs75899889 | snp | A/G | 0.261056 | 0.249755 | intron-variant | PWP1 | GRCh38.p7 | 12:107705847 | ACTATATGTATGTGC[A/G]CATATGCACATACGT | 11137 |
rs75924648 | snp | A/T | 0.0452528 | 0.143452 | intron-variant | PWP1 | GRCh38.p7 | 12:107686486 | AATTTCTTGCAGTAA[A/T]CCAAGTGAGATGTTG | 11137 |
rs75926189 | snp | C/T | 0.5 | 0 | intron-variant | PWP1 | GRCh38.p7 | 12:107708336 | TTCTTTATCCTTTTT[C/T]CTTGTACTGGCTGTT | 11137 |
rs76001780 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107705851 | TATGTATGTGCACAT[A/G]TGCACATACGTGTGC | 11137 |
rs76109550 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PWP1 | GRCh38.p7 | 12:107695474 | AAATCCTTAATTTAT[C/T]ATATATTTACCTCCT | 11137 |
rs76190892 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PWP1 | GRCh38.p7 | 12:107705387 | GTTTTTTTTTTTTTT[A/T]AAATTTAAGTTCTAG | 11137 |
rs76341373 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107694195 | CTGGCGCACTCTGCC[A/T]ACAGATTCTCCGTTT | 11137 |
rs76915756 | in-del | -/CAAAAAAAAAAAAAAAAAA | | | intron-variant | PWP1 | GRCh38.p7 | 12:107686969 | AGTGAGACTCCGTCT[-/CAAAAAAAAAAAAAAAAAA]AAAAAAAAAAAAATA | 11137 |
rs77013850 | snp | A/C | 0.5 | 0 | intron-variant | PWP1 | GRCh38.p7 | 12:107699970 | TATGGCAGAAAGCAA[A/C]TGAGGAGCAAAGTCA | 11137 |
rs77123173 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107705854 | GTATGTGCACATATG[C/T]ACATACGTGTGCATG | 11137 |
rs77239630 | snp | A/C | 0.5 | 0 | intron-variant | PWP1 | GRCh38.p7 | 12:107686969 | AGTGAGACTCCGTCT[A/C]AAAAAAAAAAAAAAA | 11137 |
rs77478466 | snp | C/T | 0.004574 | 0.0476033 | synonymous-codon, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107692857 | GGGTCTTACGGTCTA[C/T]GGGAGTAATGATCAA | 11137 |
rs77508758 | snp | C/T | | | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107685345 | GCTAAATGTTTTTTT[C/T]TCACTTTTTTTTTTG | 11137 |
rs77583795 | snp | A/T | 0.238171 | 0.24972 | intron-variant | PWP1 | GRCh38.p7 | 12:107686502 | CCAAGTGAGATGTTG[A/T]TGGTAGCAGGGAGGA | 11137 |
rs77789534 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | PWP1 | GRCh38.p7 | 12:107689904 | GTATAACGATAAATG[A/G]AAAAGGAGCTGACAA | 11137 |
rs77828333 | snp | A/G | 0.375 | 0.216506 | intron-variant | PWP1 | GRCh38.p7 | 12:107688153 | CAGAGATGGTTGGAA[A/G]AAAACCAGACGAGTA | 11137 |
rs78019596 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107685806 | GCCCTGGCAGCGGCC[C/T]TGTGCAGATCCCTGA | 11137 |
rs78317351 | snp | G/T | 0.5 | 0 | intron-variant | PWP1 | GRCh38.p7 | 12:107689015 | GATCTAAAAAAAAAA[G/T]TACTGTGTATTTTAT | 11137 |
rs78614387 | snp | A/G | 0.11228 | 0.208646 | intron-variant | PWP1 | GRCh38.p7 | 12:107695556 | TCAGTGTTTCACTGT[A/G]TAATTTTTAAAAGAC | 11137 |
rs78812895 | snp | A/T | 0.128632 | 0.218563 | intron-variant | PWP1 | GRCh38.p7 | 12:107691746 | CTCCATCTGAATTGA[A/T]TTTTATTGTCATTTA | 11137 |
rs79017589 | snp | A/C | 0.5 | 0 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107685071 | CACGAGTTCTAACAG[A/C]TGACTGATCTTAGCT | 11137 |
rs79432920 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PWP1 | GRCh38.p7 | 12:107687539 | CTGGGAACCACTATT[C/T]GAAGAGTTTATAGGA | 11137 |
rs79537229 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | PWP1 | GRCh38.p7 | 12:107695866 | AACATTATGAACTTA[C/T]GAACATTTGTTTTCT | 11137 |
rs79589033 | snp | A/C | 0.5 | 0 | intron-variant | PWP1 | GRCh38.p7 | 12:107686971 | TGAGACTCCGTCTCA[A/C]AAAAAAAAAAAAAAA | 11137 |
rs79643667 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PWP1 | GRCh38.p7 | 12:107689150 | TGCAGTCAGTCTTCT[C/T]ACAATACAGTAGTCC | 11137 |
rs80153445 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | PWP1 | GRCh38.p7 | 12:107697019 | TAACCACATCTGCAC[A/C]CTATTAGTTGCCCCT | 11137 |
rs80158745 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | PWP1 | GRCh38.p7 | 12:107712057 | TAGTGTCTTTTTATA[C/T]TCTGACTTAATTTCC | 11137 |
rs80191796 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | PWP1 | GRCh38.p7 | 12:107694610 | TCTTTGAACTTTTAC[A/G]TATTTCAAATGAAAA | 11137 |
rs80287442 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | PWP1 | GRCh38.p7 | 12:107699679 | CCTCTCTCCACCACC[A/G]CTGGAAAAAAACAGG | 11137 |
rs111236288 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | PWP1 | GRCh38.p7 | 12:107687039 | GAGTCGACATGTGCA[C/T]ATATAGTATGTCAGT | 11137 |
rs111659151 | snp | A/T | 0 | 0 | intron-variant | PWP1 | GRCh38.p7 | 12:107702411 | TCAGCCTCCTGAGTA[A/T]CTGGGATTACAGGCA | 11137 |
rs111686269 | snp | A/G | 0.5 | 0 | missense | PWP1 | GRCh38.p7 | 12:107709125 | GGTCTTGATCTTAGC[A/G]GTCAAATCAAGGGCT | 11137 |
rs111906188 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | PWP1 | GRCh38.p7 | 12:107688103 | TGTTAAGGAATGCCC[A/G]CAGGGAAGAGAGGGA | 11137 |
rs112076594 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | PWP1 | GRCh38.p7 | 12:107697877 | AGATGAAGGACTTTC[A/G]GATTATGAGCCTCCT | 11137 |
rs112376789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107709306 | CTGGAACTTGTGTTG[C/T]GTGTTTTTCTGTTGG | 11137 |
rs112383384 | snp | G/T | 0.5 | 0 | intron-variant | PWP1 | GRCh38.p7 | 12:107702590 | GGCTGTGAATCAGCT[G/T]GTCACTTTCTGTAAA | 11137 |
rs112962159 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | PWP1 | GRCh38.p7 | 12:107695593 | CTCATTGATTTTACA[A/G]TGTTTTTGCTGCTTA | 11137 |
rs113344620 | snp | A/G | 0.00324505 | 0.0401497 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107688797 | ATGATGAGGAAGGTG[A/G]CCCAGGTTAGTTTAT | 11137 |
rs113358720 | snp | A/G | 0.5 | 0 | intron-variant | PWP1 | GRCh38.p7 | 12:107690837 | TGTGTTCATTTTTCA[A/G]AATTTCTATAATACA | 11137 |
rs113800653 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | PWP1 | GRCh38.p7 | 12:107690506 | TCTTGCTCTGTTGCC[C/T]AGGCTAGAGTGCTGT | 11137 |
rs113842131 | snp | C/G | 0.5 | 0 | intron-variant | PWP1 | GRCh38.p7 | 12:107698631 | CTCTGTCTCCCAAGA[C/G]TGGAGTGCAGTGGCA | 11137 |
rs113889442 | snp | C/T | 0.5 | 0 | synonymous-codon | PWP1 | GRCh38.p7 | 12:107708931 | CTCTTTCTAGGCCAG[C/T]ACAGATGACGGCTTT | 11137 |
rs113945727 | snp | C/T | 0.5 | 0 | intron-variant | PWP1 | GRCh38.p7 | 12:107702722 | TTAAGTCTTCTAATA[C/T]ATGAACATGGGGTTT | 11137 |
rs114012327 | snp | A/G | 0.021333 | 0.101051 | intron-variant | PWP1 | GRCh38.p7 | 12:107699219 | AGCTGAGATCGTGCA[A/G]CTGCACTCTAGCCAG | 11137 |
rs114021119 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | PWP1 | GRCh38.p7 | 12:107692217 | AACAATTCAGTGTAT[C/T]TTCCTTTTCCTGAGT | 11137 |
rs114023745 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | PWP1 | GRCh38.p7 | 12:107693920 | ACATTTTATTTTCTT[C/T]CTAATAATTCAACAC | 11137 |
rs114136548 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | PWP1 | GRCh38.p7 | 12:107691824 | TGGCCATCTGTCCTA[C/T]GGATTACTATTAACT | 11137 |
rs114355539 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | PWP1 | GRCh38.p7 | 12:107700311 | AACATTTTCATCTCC[A/G]TACTGCAGCTCTGCC | 11137 |
rs114513207 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | PWP1 | GRCh38.p7 | 12:107701977 | GCCACCGCGCCCAGC[C/T]CCATTTGTTAAGACT | 11137 |
rs114730069 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | PWP1 | GRCh38.p7 | 12:107704974 | GCCATTCCAAAGTGT[A/G]CCACGTTTTATTTAA | 11137 |
rs114827549 | snp | C/T | 0.00437519 | 0.0465667 | intron-variant | PWP1 | GRCh38.p7 | 12:107703678 | CATTTATGTTTCCTC[C/T]CTTTAGGTCCAAACA | 11137 |
rs114897608 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | PWP1 | GRCh38.p7 | 12:107705080 | AAATCAGTCCAAGAT[G/T]ATATTCTTTTCTTTA | 11137 |
rs115257200 | snp | C/T | 0.11228 | 0.208646 | intron-variant | PWP1 | GRCh38.p7 | 12:107711456 | GATCTTTGGGGAAAG[C/T]TGGAAAGAAATATAG | 11137 |
rs115770686 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | PWP1 | GRCh38.p7 | 12:107708777 | GTGCAAACTCAGGTC[A/G]TCCAAAAGTAAATGA | 11137 |
rs116174656 | snp | A/G | 0.00323446 | 0.0400845 | intron-variant | PWP1 | GRCh38.p7 | 12:107692770 | AAATATGTTTTTGTC[A/G]AGATGACTATTTTAT | 11137 |
rs116315589 | snp | A/G | 0.0182019 | 0.0936463 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107685019 | TTTTTCTGGGATGCT[A/G]GTTTGAGATTTTCCA | 11137 |
rs116573756 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | PWP1 | GRCh38.p7 | 12:107691631 | TTTAGCATCATCCTA[A/G]TGGATGAACTCTCTT | 11137 |
rs116646266 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107705123 | TAAATGGATCTCTAG[A/T]GATGAGAATGCTAAC | 11137 |
rs116814327 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | PWP1 | GRCh38.p7 | 12:107695966 | ATTTTCTCCTGTGGG[G/T]TATGCCACAAGATGG | 11137 |
rs116950789 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | PWP1 | GRCh38.p7 | 12:107687629 | GGACAAGCCAGTTGC[A/G]GTGGCTCGTGCCTGT | 11137 |
rs116984237 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | PWP1 | GRCh38.p7 | 12:107700605 | CTTCTTCTGCCTTTT[A/G]GATACTGTGAATAAT | 11137 |
rs117153094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107709890 | TTGCCTAAATGCTTA[C/T]ATTTAACTCTAGTAG | 11137 |
rs117231086 | snp | A/G | 0.0218212 | 0.102149 | utr-variant-5-prime, missense | PWP1 | GRCh38.p7 | 12:107688476 | AAGAAGAAGTAAAAC[A/G]CCTCATTGCTGAGGC | 11137 |
rs117515660 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PWP1 | GRCh38.p7 | 12:107700606 | TTCTTCTGCCTTTTG[A/G]ATACTGTGAATAATG | 11137 |
rs117963602 | snp | A/G | 0.000527348 | 0.0162295 | missense | PWP1 | GRCh38.p7 | 12:107710481 | AAAAAGAAGGGCTTC[A/G]GGTCTGGGATATAAG | 11137 |
rs117995580 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PWP1 | GRCh38.p7 | 12:107700881 | GTGGTATATCATTGC[A/G]GTTTTAATTTGCATT | 11137 |
rs118049386 | snp | A/G/T | 0.0456336 | 0.143994 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107685173 | GTGTGACCTTTGGAA[A/G/T]GATCGCTGTTTTCCC | 11137 |
rs118171831 | snp | A/G | 0.0165278 | 0.0893908 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107684053 | AGGCTTCCCCAGCCA[A/G]CTGAAACTGTGAGTC | 11137 |
rs137862280 | snp | A/C | | | intron-variant | PWP1 | GRCh38.p7 | 12:107695099 | TCTCTACTAAAAATA[A/C]AAAAAAAAAAAAAAA | 11137 |
rs137989607 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PWP1 | GRCh38.p7 | 12:107686682 | ACAAAATAGAAAAAG[C/T]CCCGCCGGGCGCGGT | 11137 |
rs138034608 | snp | C/T | 0.00138426 | 0.026272 | intron-variant | PWP1 | GRCh38.p7 | 12:107703770 | GCACAGCAAGAATGA[C/T]TGCTACTCTGTTTTT | 11137 |
rs138303440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107711882 | CATTTGTTACCAAGG[C/T]GGATCAGATAAATCC | 11137 |
rs138384840 | snp | C/G | 1.64898e-05 | 0.00287135 | missense | PWP1 | GRCh38.p7 | 12:107702994 | GGGATATGTCCTTGG[C/G]GAAACCAGCAGCTAG | 11137 |
rs138511413 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107684096 | TTTTCTTTATAAATT[A/G]TCATGTCTTGGGTAT | 11137 |
rs138526290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107691257 | AGGAGGGGAAATGCT[C/T]GGCAAGTTGATCTGC | 11137 |
rs138617524 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PWP1 | GRCh38.p7 | 12:107694500 | CTGTCCGTGGGAAGC[C/T]TATAGATTAGGCCCA | 11137 |
rs138804785 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PWP1 | GRCh38.p7 | 12:107695182 | GAGGCAGGAGAATGG[C/T]GTGAACCTGGGAGGC | 11137 |
rs138877865 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107702171 | GGAAATATGAACTTG[A/C]CAACTTTGTTCTTTT | 11137 |
rs138878573 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PWP1 | GRCh38.p7 | 12:107711528 | GTGAATAAATCCACC[A/G]TTTGCTCAACTATAA | 11137 |
rs138941787 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | PWP1 | GRCh38.p7 | 12:107698894 | GCTGCACCCAGCCCC[C/T]GTAATGAAATTAATC | 11137 |
rs139101942 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | PWP1 | GRCh38.p7 | 12:107698980 | ATAATATCAAAACAA[C/T]AGGTCGGGTGCAGTA | 11137 |
rs139208791 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | PWP1 | GRCh38.p7 | 12:107691605 | AAAGGGATTGCAGAG[A/G]TAGCTGGGAGTTTAG | 11137 |
rs139223928 | snp | C/G | 0.00358779 | 0.0422022 | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712630 | GAGGCCATGAACAGA[C/G]GCAAGTGCCCCAGAG | 11137 |
rs139243505 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107700284 | GCAACCATCACCACA[A/G]TGCATCTCCAGAACA | 11137 |
rs139258450 | snp | A/G | 6.5937e-05 | 0.00574144 | missense | PWP1 | GRCh38.p7 | 12:107710462 | ATTTATGCCTTTGGA[A/G]GTCAAAAAGAAGGGC | 11137 |
rs139301430 | snp | G/T | 1.64933e-05 | 0.00287165 | missense | PWP1 | GRCh38.p7 | 12:107704718 | ATAGAGAGAGTGACT[G/T]GGAATCACTTTTCAC | 11137 |
rs139317682 | snp | A/C/G | 0.00057711 | 0.0169773 | synonymous-codon, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107692851 | TCTCTTGGGTCTTAC[A/C/G]GTCTACGGGAGTAAT | 11137 |
rs139350050 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PWP1 | GRCh38.p7 | 12:107704850 | TTTCTGTTTTAACAG[A/T]ATGAAGTATTTGGGT | 11137 |
rs139376750 | snp | A/C/G | 3.29697e-05 | 0.00406005 | synonymous-codon | PWP1 | GRCh38.p7 | 12:107702953 | TGTTTTAGCAAGTGC[A/C/G]TCAGCTGACAACACT | 11137 |
rs139441642 | snp | A/G | 0.0277655 | 0.114507 | intron-variant | PWP1 | GRCh38.p7 | 12:107709084 | CTGTATTTCAAAGCG[A/G]AAGTGTCTAAACTTA | 11137 |
rs139780863 | in-del | -/A | 0.487746 | 0.0773096 | intron-variant | PWP1 | GRCh38.p7 | 12:107695100 | AAAAAAAAAAAAAAA[-/A]TCAGCCAGGCGTGGT | 11137 |
rs139922249 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PWP1 | GRCh38.p7 | 12:107708776 | AGTGCAAACTCAGGT[C/T]GTCCAAAAGTAAATG | 11137 |
rs139981282 | snp | A/G | 0.000131978 | 0.0081223 | synonymous-codon, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107688681 | TGGCATGCAGAGTGC[A/G]CGCACCCAGGCACGC | 11137 |
rs140013921 | snp | A/G | 0.00049456 | 0.0157174 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107693070 | GTGGCCGAGCTGAAC[A/G]GGACCAGTGCAATTT | 11137 |
rs140044260 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PWP1 | GRCh38.p7 | 12:107704038 | GGGCATGGATATAGG[A/G]AGACATGAAGAACTG | 11137 |
rs140205385 | snp | A/G | | | missense | PWP1 | GRCh38.p7 | 12:107697490 | ATTGCTGTAGGAAAC[A/G]TGACCCCTGTTATTG | 11137 |
rs140355528 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | PWP1 | GRCh38.p7 | 12:107710992 | ACACACACAGAAATA[C/T]AGAGATGTGAAGTGG | 11137 |
rs140479080 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | PWP1 | GRCh38.p7 | 12:107711538 | CCACCGTTTGCTCAA[C/T]TATAAAATTCTACAA | 11137 |
rs140548292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107691806 | CCGTTTTCCTCATTC[A/G]CTTGGCCATCTGTCC | 11137 |
rs140607734 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PWP1 | GRCh38.p7 | 12:107693659 | TTGCTCGAGCCCATG[A/G]GTTCTAGGCTACAGT | 11137 |
rs140695212 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PWP1 | GRCh38.p7 | 12:107692249 | ATCCTTTGTTACCAT[C/T]GTAGATGTGCCATAA | 11137 |
rs140811362 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | PWP1 | GRCh38.p7 | 12:107706709 | AAGATCAGATGATTG[C/T]AGATGTGTGGTATTA | 11137 |
rs140836989 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107695716 | TTTTAAAAATATTAA[C/G]AGTAATTTTTGATAA | 11137 |
rs141217040 | snp | A/C/G | 0.000149307 | 0.00863893 | synonymous-codon, missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107688736 | GACCCAGAGGATGAC[A/C/G]GGACGCTTGATGATG | 11137 |
rs141233771 | snp | A/C | | | intron-variant | PWP1 | GRCh38.p7 | 12:107705522 | CTATCCCTCCCCCTC[A/C]CCCCACCCCACGACA | 11137 |
rs141341682 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | PWP1 | GRCh38.p7 | 12:107696691 | GAATTGTTGCTGATA[C/T]TTTCTGAAGTTACTG | 11137 |
rs141375759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107694109 | TAATATTAATTGAAT[A/G]GCTTGCCTCACTTTG | 11137 |
rs141450163 | snp | C/T | 0.00925511 | 0.0673936 | missense | PWP1 | GRCh38.p7 | 12:107702985 | TAATTCTGTGGGATA[C/T]GTCCTTGGGGAAACC | 11137 |
rs141464716 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107699133 | GCATGGTGGCATGCG[C/T]GTGTAATCCCAGCTA | 11137 |
rs141495217 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | PWP1 | GRCh38.p7 | 12:107694923 | TTCTAAAACTGATCC[C/G]AATATTGATCTCACG | 11137 |
rs141560924 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107691548 | CCAGAAGCAATGAGG[G/T]CCTGGCTTGGGGCAC | 11137 |
rs141739496 | in-del | -/G/GG | 0.439918 | 0.162576 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107684365 | CAAGTTGGTGGGGGC[-/G/GG]GGGGGGGGGTGCTTT | 11137 |
rs141781350 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PWP1 | GRCh38.p7 | 12:107694988 | TTGCTGGGCGTAGTG[A/G]CTCATGCTTGTAATC | 11137 |
rs141826419 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107703974 | CTTCTTTGGCTTTTA[G/T]AGGCTGTACTTTGCC | 11137 |
rs141919063 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PWP1 | GRCh38.p7 | 12:107708538 | TTGACTGTTGGTCAC[A/G]CCTTGGTTCCTTGAC | 11137 |
rs141986082 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PWP1 | GRCh38.p7 | 12:107708089 | GACTTATTTTTACAA[C/T]GATCATTCCAGTTGT | 11137 |
rs142231100 | snp | A/C | 0.000153988 | 0.00877328 | synonymous-codon | PWP1 | GRCh38.p7 | 12:107710413 | TCTCTAGGGAGTTCT[A/C]TTCTGTTCTTCATGT | 11137 |
rs142242514 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PWP1 | GRCh38.p7 | 12:107704385 | GAGGATTCTTCTTGC[A/G]AGTGGAAGATTTGAC | 11137 |
rs142279582 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | PWP1 | GRCh38.p7 | 12:107693479 | CACCACACCTGGCCT[C/G]ATAGAGGTTTTTAAT | 11137 |
rs142377319 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PWP1 | GRCh38.p7 | 12:107689178 | TCCCCCCTTATCCAC[A/G]GTTTTGCTTTCTTCG | 11137 |
rs142551881 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PWP1 | GRCh38.p7 | 12:107701666 | TGAGGATGATTCATT[C/T]GTCCCTGAACCATTT | 11137 |
rs142576721 | snp | C/T | 1.65211e-05 | 0.00287407 | synonymous-codon | PWP1 | GRCh38.p7 | 12:107699393 | CTCAGCAGAAGGGCA[C/T]ACCGATGCTGTCCTT | 11137 |
rs142592988 | snp | C/T | 0.000216063 | 0.0103916 | missense | PWP1 | GRCh38.p7 | 12:107708927 | TTTACTCTTTCTAGG[C/T]CAGTACAGATGACGG | 11137 |
rs142635199 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PWP1 | GRCh38.p7 | 12:107688163 | TGGAAGAAAACCAGA[C/T]GAGTACCACACAGCC | 11137 |
rs142648803 | snp | C/T | | | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107685164 | TTACTAGCAGTGTGA[C/T]CTTTGGAAGGATCGC | 11137 |
rs142712012 | in-del | -/ACATATGCACATACGTGT | 0.354019 | 0.227333 | intron-variant | PWP1 | GRCh38.p7 | 12:107705847 | ACTATATGTATGTGC[-/ACATATGCACATACGTGT]GCATGTGTCTTTATA | 11137 |
rs142789452 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PWP1 | GRCh38.p7 | 12:107698949 | GTTTTATTTATTTTA[C/T]TCTTCAAAAGTTTAT | 11137 |
rs142823124 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | PWP1 | GRCh38.p7 | 12:107695244 | GCACTCCAGCCTGGG[C/T]GACAGAGCAAGACTC | 11137 |
rs142974855 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PWP1 | GRCh38.p7 | 12:107696246 | TTGTGTTGGCCAGGC[C/T]GGTCTCGAACTCCTG | 11137 |
rs143110941 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107709927 | TCCCAGAACATAAAC[C/T]GTGGTTACCTCCCTG | 11137 |
rs143176509 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107698874 | CTGGGATTACAGTGT[A/G]GGCCGCTGCACCCAG | 11137 |
rs143251342 | snp | C/T | 0.00478085 | 0.0486577 | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712647 | CAAGTGCCCCAGAGA[C/T]TCCACTTTCATTCCT | 11137 |
rs143258538 | in-del | -/T | 0.467231 | 0.123737 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107685337 | AATTGGTGCTAAATG[-/T]TTTTTTTCTCACTTT | 11137 |
rs143455193 | in-del | -/TTA | 0.11228 | 0.208646 | intron-variant | PWP1 | GRCh38.p7 | 12:107691674 | CGTCTGGTTTCCATC[-/TTA]TTATCGCTGGTGTAC | 11137 |
rs143457477 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PWP1 | GRCh38.p7 | 12:107694936 | CCGAATATTGATCTC[A/T]CGTGGTTAAGAGTAT | 11137 |
rs143711289 | snp | A/G | 1.65181e-05 | 0.00287381 | synonymous-codon | PWP1 | GRCh38.p7 | 12:107697510 | CCCTGTTATTGAAGT[A/G]TGGGACCTTGATATA | 11137 |
rs143776807 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107690099 | ACAGCTAGAATCAGC[G/T]ACTCCCAAGTTATAA | 11137 |
rs143815113 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107697064 | ATAAAGGTAAACACT[A/G]TTTATACTGTCTTAC | 11137 |
rs144046612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107691789 | TCTAGATGTTCATTC[C/T]TCCGTTTTCCTCATT | 11137 |
rs144157331 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107705619 | GTGAGAACATGCAAC[A/G]TTTGGTTTTCTGTCC | 11137 |
rs144278078 | in-del | -/TTAG | | | intron-variant | PWP1 | GRCh38.p7 | 12:107705307 | CATCCAGAGCAAAGA[-/TTAG]TTAAATTTGTTGCCC | 11137 |
rs144416124 | snp | A/G | 0.0150606 | 0.0854603 | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712378 | GCACCACAAATATCC[A/G]GTCTTTGTGCTTGCT | 11137 |
rs144651706 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | PWP1 | GRCh38.p7 | 12:107694294 | CCCCAGCAGTCTTCA[G/T]ATCGTCTTGAAACTT | 11137 |
rs144718170 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PWP1 | GRCh38.p7 | 12:107690913 | GTGGGGTATCTGGAA[A/G]AGCAGTGTAGTTGGA | 11137 |
rs144931576 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | PWP1 | GRCh38.p7 | 12:107705179 | AAATAGGAAAAAAAG[C/T]ATAAGACCTCTGTCT | 11137 |
rs145045729 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107709669 | ATAGTAGGAAAAATT[G/T]AGAAATAACCAGATT | 11137 |
rs145046287 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PWP1 | GRCh38.p7 | 12:107711094 | CAAACTAGTCTTTAG[C/T]ATTGTTTCTATAGGT | 11137 |
rs145064281 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | PWP1 | GRCh38.p7 | 12:107709806 | ATAAATATATATAAA[C/T]ATAATGGAAAAACAG | 11137 |
rs145080111 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | PWP1 | GRCh38.p7 | 12:107707861 | TTGGTCTAAAATTCT[C/G]TTTTTTCGTTGTGTC | 11137 |
rs145343270 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107693968 | TTTTGGAACCAAAAC[A/G]TCGTGATCACCTTTC | 11137 |
rs145716869 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | PWP1 | GRCh38.p7 | 12:107697495 | TGTAGGAAACATGAC[C/T]CCTGTTATTGAAGTG | 11137 |
rs145882899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107689606 | CAAAACTTAGCCAGG[C/T]GTGGTGGCGCACATC | 11137 |
rs145941088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107687279 | GTTACATTTATAGAA[C/T]AGGGACAGAAAATTA | 11137 |
rs146061270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107704017 | ATTTCCATGTCACAT[A/G]ACAGAGGGCATGGAT | 11137 |
rs146142854 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | PWP1 | GRCh38.p7 | 12:107700964 | CAAATTCTTGGGCTC[A/C]AGCAATCCCCCCGCC | 11137 |
rs146226600 | snp | G/T | 9.89985e-05 | 0.00703487 | missense | PWP1 | GRCh38.p7 | 12:107704648 | TAGGTCAGTGGCTTT[G/T]TATGACTGCCGAAGT | 11137 |
rs146383833 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PWP1 | GRCh38.p7 | 12:107708127 | TGTTGTGTTGTACTT[C/T]GGCTCTCACTCTTCA | 11137 |
rs146401348 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PWP1 | GRCh38.p7 | 12:107704548 | TGAATCTTGATTTCA[C/T]AGTGCTATTTTATTA | 11137 |
rs146531497 | snp | A/C/G | 1.64912e-05 | 0.00287147 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107692858 | GGTCTTACGGTCTAC[A/C/G]GGAGTAATGATCAAG | 11137 |
rs146643929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107696348 | TGGAATCTCTTTATA[A/G]TATCAGATGTCTCAC | 11137 |
rs146687104 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | PWP1 | GRCh38.p7 | 12:107697143 | TCCCCACAGCACCCC[A/G]TGAAGGAGGACGGGA | 11137 |
rs146836947 | snp | C/G | 1.64749e-05 | 0.00287005 | missense | PWP1 | GRCh38.p7 | 12:107712174 | GAAATTCATCTATTA[C/G]TGGCCCTTTTGGCAG | 11137 |
rs146897475 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107689369 | TCTGTGGTTTTAGAC[C/T]ACCACTGAGGGTCTT | 11137 |
rs146953465 | in-del | -/TCAC | 0.0232847 | 0.105357 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107685300 | TTTGCCAAGACTAAA[-/TCAC]TACTGCATAGTTAGT | 11137 |
rs147021387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107703156 | GCGGCATGCTTTCAC[A/G]TGTTATCTCTTAGGA | 11137 |
rs147041749 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107683914 | GGGATTACAGGCATG[A/C]GCCACTGCACCCAGC | 11137 |
rs147370373 | snp | C/T | 0.0189856 | 0.0955633 | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712771 | TGATATTCACTGTTA[C/T]CAAAGACAAGAGGCA | 11137 |
rs147405132 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107698970 | AAAAGTTTATATAAT[A/C]TCAAAACAATAGGTC | 11137 |
rs147700292 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PWP1 | GRCh38.p7 | 12:107692213 | CTCTAACAATTCAGT[G/T]TATCTTCCTTTTCCT | 11137 |
rs147705027 | snp | C/T | 0.000307953 | 0.0124049 | synonymous-codon | PWP1 | GRCh38.p7 | 12:107712115 | TTGTATTTTAGTAAA[C/T]GAAGCATTTGGAAGA | 11137 |
rs147805980 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107708814 | TCCATGTTAATTTTT[C/T]ATAAGTTCCACCAGT | 11137 |
rs147956172 | in-del | -/TAG | | | intron-variant | PWP1 | GRCh38.p7 | 12:107687001 | AAAAAAAAAAAAAAA[-/TAG]AAAAAGACCCTGCCT | 11137 |
rs147995707 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | PWP1 | GRCh38.p7 | 12:107690123 | GTTATAAAATCAAAA[G/T]GTAGATGATCGGAAA | 11137 |
rs148049526 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PWP1 | GRCh38.p7 | 12:107694981 | TTACCAGTTGCTGGG[C/T]GTAGTGACTCATGCT | 11137 |
rs148117877 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PWP1 | GRCh38.p7 | 12:107703914 | CCTTTCAGTCTACAA[C/T]GGAACATGATTCTGT | 11137 |
rs148349473 | snp | A/C | 0.00835141 | 0.0640778 | utr-variant-5-prime, intron-variant | PWP1 | GRCh38.p7 | 12:107686044 | GCCCAGCTGGGGGAA[A/C]GTGGACCCGGAACTC | 11137 |
rs148590716 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PWP1 | GRCh38.p7 | 12:107708251 | TGGTTCACCTGCTTC[C/T]CTCTCATCTCAAAAG | 11137 |
rs148629471 | snp | A/C/T | 0.000280463 | 0.0118388 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107688682 | GGCATGCAGAGTGCA[A/C/T]GCACCCAGGCACGCC | 11137 |
rs148638337 | snp | C/T | 0.0991586 | 0.199366 | intron-variant | PWP1 | GRCh38.p7 | 12:107705505 | AGGTATATCTCCTAA[C/T]GCTATCCCTCCCCCT | 11137 |
rs148682004 | snp | C/T | 6.59304e-05 | 0.00574116 | synonymous-codon | PWP1 | GRCh38.p7 | 12:107709196 | GGACATCTTAGGAGA[C/T]AGGCCAAGTCTAGTT | 11137 |
rs148712905 | in-del | -/TTCT | 0.0209421 | 0.100162 | intron-variant | PWP1 | GRCh38.p7 | 12:107708429 | TAATTCCTTCATTTC[-/TTCT]TTCTTTCTTGACAGT | 11137 |
rs148947517 | snp | C/T | 3.30628e-05 | 0.00406575 | missense | PWP1 | GRCh38.p7 | 12:107697503 | ACATGACCCCTGTTA[C/T]TGAAGTGTGGGACCT | 11137 |
rs148971597 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | PWP1 | GRCh38.p7 | 12:107689915 | AATGGAAAAGGAGCT[A/G]ACAAAGCTCGCTTTG | 11137 |
rs148992954 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | PWP1 | GRCh38.p7 | 12:107701563 | TCTGAGTTTTATAGT[A/G]TTAGCTCTTACATTG | 11137 |
rs149040271 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | PWP1 | GRCh38.p7 | 12:107698514 | ACCTGGGTGACAGAG[C/T]GAGATTTTGTCTCTA | 11137 |
rs149112922 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | PWP1 | GRCh38.p7 | 12:107709908 | TTAACTCTAGTAGAT[G/T]ATATCCCAGAACATA | 11137 |
rs149261306 | snp | A/T | 1.64838e-05 | 0.00287083 | missense | PWP1 | GRCh38.p7 | 12:107703739 | CTGATTTCTGGCTCA[A/T]ATGATAAGTAAGAAA | 11137 |
rs149412345 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107688111 | AATGCCCACAGGGAA[A/G]AGAGGGAGAGGTGCC | 11137 |
rs149469533 | snp | C/T | 0.000265155 | 0.0115112 | utr-variant-5-prime, missense | PWP1 | GRCh38.p7 | 12:107688475 | AAAGAAGAAGTAAAA[C/T]GCCTCATTGCTGAGG | 11137 |
rs149497660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107691734 | CTGATTTCCTCACTC[C/T]ATCTGAATTGATTTT | 11137 |
rs149518446 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PWP1 | GRCh38.p7 | 12:107703819 | TAAGAGTATCACTTG[A/G]TACCCAGGCAGAATG | 11137 |
rs149637510 | snp | G/T | 8.24586e-05 | 0.00642047 | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712227 | GAGTCTTAATGAAGA[G/T]CATCTAATTTCCTGC | 11137 |
rs149781500 | snp | A/C | 0.000230821 | 0.0107405 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107696490 | TTATAATCAAGAAGA[A/C]GACTCTTTTTATGTA | 11137 |
rs149974974 | in-del | -/CTGA | | | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712331 | AAACACAATTCATTT[-/CTGA]CTGACTGACATTCCT | 11137 |
rs149992578 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107700310 | GAACATTTTCATCTC[C/T]GTACTGCAGCTCTGC | 11137 |
rs150146447 | snp | C/G | 0.0349115 | 0.127424 | intron-variant | PWP1 | GRCh38.p7 | 12:107706844 | AGCATGATGCCTCCA[C/G]CTTTGTTCTTTTGGC | 11137 |
rs150277608 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | PWP1 | GRCh38.p7 | 12:107687759 | AATTAAGGCCGGGCA[C/T]GGTGGCTCACGCCTG | 11137 |
rs150402979 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107711843 | AGAATAAGGCCAGGA[G/T]AGGGTCACTTATAAG | 11137 |
rs150601160 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | PWP1 | GRCh38.p7 | 12:107695073 | ATCCTGGCTAACACG[G/T]TAAAACCCAGTCTCT | 11137 |
rs150668847 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PWP1 | GRCh38.p7 | 12:107708547 | GGTCACGCCTTGGTT[C/T]CTTGACACTCTTCCC | 11137 |
rs150740491 | snp | G/T | 0.0150606 | 0.0854603 | utr-variant-5-prime, intron-variant | PWP1 | GRCh38.p7 | 12:107686116 | TGCCCGGATTGTCGC[G/T]ACTAGAGCTGCAGTT | 11137 |
rs150794362 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | PWP1 | GRCh38.p7 | 12:107691601 | GAAGAAAGGGATTGC[A/G]GAGGTAGCTGGGAGT | 11137 |
rs150864562 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107699711 | TGTTTGGCAGTGCCC[A/G]TGGTGCAGTAGGATT | 11137 |
rs150966577 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PWP1 | GRCh38.p7 | 12:107701803 | CTGCCTCAGCCTCCT[A/G]AGTAGCTGGGATTAC | 11137 |
rs151019878 | snp | A/G | 0.142609 | 0.225759 | intron-variant | PWP1 | GRCh38.p7 | 12:107706382 | ttcttttgctgtgca[A/G]aagctctttagttta | 11137 |
rs151080047 | in-del | -/G | 0.0162398 | 0.0886349 | intron-variant | PWP1 | GRCh38.p7 | 12:107707897 | CGGGCTTTGGTATCA[-/G]GGTGATGCTGGCCTC | 11137 |
rs151194435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107710958 | ACCCTAACCCAGTGG[C/T]GCTAGAGGAATTAAA | 11137 |
rs151235634 | snp | C/T | 1.64863e-05 | 0.00287104 | synonymous-codon | PWP1 | GRCh38.p7 | 12:107710437 | TTCATGTTGCCCTGA[C/T]TTGCCATTTATTTAT | 11137 |
rs151265502 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | PWP1 | GRCh38.p7 | 12:107688395 | ACTTTTTAATTCAAA[A/T]AATTTGATGATTTCC | 11137 |
rs151318184 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PWP1 | GRCh38.p7 | 12:107693599 | GGCTGGGTGCGGTGT[C/G]TCACACCTGTAATCC | 11137 |
rs180871646 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PWP1 | GRCh38.p7 | 12:107711663 | CAGAGATAATATATA[C/T]ATCTCCCCACTGTAT | 11137 |
rs180989848 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PWP1 | GRCh38.p7 | 12:107707568 | TATTTTGAGATATGT[C/T]TCATCAATACCGAAT | 11137 |
rs181001862 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PWP1 | GRCh38.p7 | 12:107688005 | CATTGCTCTTCAGCC[C/T]GGGCAACAGAGCGAG | 11137 |
rs181031569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107698205 | TGTCTCTACTAAATA[C/T]ACAAAAATTAGCCAG | 11137 |
rs181154033 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107691460 | TTTAGGAAGTTAACT[C/G]TGGCAACAGTGGAGA | 11137 |
rs181160293 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PWP1 | GRCh38.p7 | 12:107710143 | GAGACAGAGTGATAA[C/T]GAAGATGAGTGGCCT | 11137 |
rs181282406 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107706766 | TGGTCTACATCTCTG[G/T]TTTGGTACCAGTACC | 11137 |
rs181301417 | snp | C/G | 0.000209205 | 0.0102254 | intron-variant | PWP1 | GRCh38.p7 | 12:107697434 | TGTATGTCTTTTTTT[C/G]TGTAATCATACATGC | 11137 |
rs181389546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107687938 | CAAGAGGCTAAGGCA[A/G]GAGAATCGCTTGAAC | 11137 |
rs181656270 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107702681 | ATAGCTCCATCTGTA[C/G]ATGTAATATTTCCAT | 11137 |
rs181666923 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107683835 | ACGGGGTTTCACTAC[A/G]TTGGCCAGGCTTGTC | 11137 |
rs181792193 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107687514 | AGGTGATTCTGATGT[A/T]CAGATAAGTCTGGGA | 11137 |
rs181799439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107706225 | CTATTCATATCCTTC[A/G]CCCACTTTTTGATGG | 11137 |
rs181868294 | snp | A/C | | | intron-variant | PWP1 | GRCh38.p7 | 12:107704071 | GCCACTGTGGTCAAC[A/C]ACGGGGTTTATAGCT | 11137 |
rs181890064 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | PWP1 | GRCh38.p7 | 12:107690682 | TGGCCGGGATGGTCT[C/G]AATCTCCTGACCTCA | 11137 |
rs181930211 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PWP1 | GRCh38.p7 | 12:107692122 | AATCAGCTCTTTCTC[A/G]TGTAGCAGAAATTGC | 11137 |
rs182137739 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107710055 | TTTAAACTGGCATCA[G/T]TGTTATTGTTTAAAA | 11137 |
rs182143188 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PWP1 | GRCh38.p7 | 12:107702294 | ATCCTGTTTTGTTTT[C/G]TTTTGAGACAGAGTC | 11137 |
rs182255838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107698812 | TGCCTGGGCTGGTCT[C/T]GAACTCCCGGCCTCA | 11137 |
rs182290340 | snp | A/G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107685667 | CCCAGACCAGCCCAC[A/G/T]TGGATTCCTCGCCCG | 11137 |
rs182385872 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712484 | TTCCTTAAACATACC[A/G]TCTGTCACAGTTAAT | 11137 |
rs182396732 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | PWP1 | GRCh38.p7 | 12:107694681 | AAAAATTGAGAACCT[A/G]TTAGAGTTTTTTTTG | 11137 |
rs182553256 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | PWP1 | GRCh38.p7 | 12:107704961 | TTGCTGGTTGCCGGC[C/G]ATTCCAAAGTGTGCC | 11137 |
rs182692948 | snp | G/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107700572 | TACCCGTTCATTTAC[G/T]TGTGGTCACCTGGAT | 11137 |
rs182831095 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107685147 | TATCCCAGCTGCACC[A/G]CTTACTAGCAGTGTG | 11137 |
rs182883562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107700531 | TTTTTAAGGCTAAAT[A/G]ATATTCCATTGTATG | 11137 |
rs183123658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107686183 | GGCCGCGCCTTCTCA[C/T]TGTTCCCACCCTCAA | 11137 |
rs183124614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107704055 | GACATGAAGAACTGG[A/G]GCCACTGTGGTCAAC | 11137 |
rs183134680 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107705370 | TGCAAAGGTGAGAAA[C/G]AGTTTTTTTTTTTTT | 11137 |
rs183248480 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107708110 | TTCCAGTTGTACTTG[A/T]ATGTTGTGTTGTACT | 11137 |
rs183401847 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107708802 | AAATGATTTCTGTCC[A/G]TGTTAATTTTTCATA | 11137 |
rs183575095 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | PWP1 | GRCh38.p7 | 12:107693185 | TTTTTAGGTGCCAGA[A/T]CCTATTGTATCTCAT | 11137 |
rs183581765 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | PWP1 | GRCh38.p7 | 12:107706050 | TTTCTCCACATCTCT[C/G]CAGCACCTGTTGTTT | 11137 |
rs183589932 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107687114 | TACTTGACCAAGATA[A/T]TGATGATGGTGATAG | 11137 |
rs183654504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107689567 | CCGGGCCAACATGGC[A/G]AAACCCTGTCTCTAC | 11137 |
rs183695882 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107690293 | GCTGAGGCAGCAGGA[A/T]CGCTCAAGCCCAGGA | 11137 |
rs183708100 | snp | C/T | 1.65551e-05 | 0.00287702 | intron-variant | PWP1 | GRCh38.p7 | 12:107709261 | TGGGTATCTGTTTTT[C/T]ATTTATTCTGTTTCT | 11137 |
rs183784053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107712054 | TTTTAGTGTCTTTTT[A/G]TATTCTGACTTAATT | 11137 |
rs183887105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107700882 | TGGTATATCATTGCG[A/G]TTTTAATTTGCATTT | 11137 |
rs183975213 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107697786 | ATTTCTGATTACATA[A/C]AACCTCCATTATCAT | 11137 |
rs184381786 | snp | A/T | 0.0240643 | 0.107019 | intron-variant | PWP1 | GRCh38.p7 | 12:107706540 | TAGGTCTAACATTTA[A/T]TTTAAGTCTTTAATC | 11137 |
rs184412146 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107701606 | CATTTTGAGTTTTTT[G/T]TGTGTGTATGGTGTG | 11137 |
rs184440049 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107695969 | TTCTCCTGTGGGGTA[A/T]GCCACAAGATGGCAC | 11137 |
rs184491751 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PWP1 | GRCh38.p7 | 12:107701188 | CTGGAGTGCAGTGGC[A/G]CAATCACTGCTCACT | 11137 |
rs184516353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107709907 | TTTAACTCTAGTAGA[C/T]TATATCCCAGAACAT | 11137 |
rs184583535 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | PWP1 | GRCh38.p7 | 12:107686760 | TCACGAGGTCAGGAG[A/G]TCGAGAGCATCCTGG | 11137 |
rs184696874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107705604 | AATTCCCACCTATGA[A/G]TGAGAACATGCAACG | 11137 |
rs185102126 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107710103 | GGAAATACATGGCAC[A/G]TTAGGTTTGTTAGGA | 11137 |
rs185216400 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107688194 | ACTTTACCAAAACCA[C/G]TCTTTGGAGTTTTAA | 11137 |
rs185226429 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | PWP1 | GRCh38.p7 | 12:107707828 | TGAGGATTTTTGCAT[C/G]GATGTTCTTCAGGGA | 11137 |
rs185233359 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107690804 | AGGTAATTCAAGGTT[C/T]GTGATGCCCTCTCCA | 11137 |
rs185246179 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107697156 | CCATGAAGGAGGACG[C/G]GAGGAGGGTTATTCT | 11137 |
rs185369295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107691660 | TTCCAGAATTGGTAC[A/G]TCTGGTTTCCATCTT | 11137 |
rs185373719 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PWP1 | GRCh38.p7 | 12:107711217 | CCTTAAGACACAGAT[C/T]GAGATCGCTCATGCT | 11137 |
rs185387083 | snp | G/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107690480 | CTTTTTTTTGTGTGT[G/T]TGAGACGGAGTCTTG | 11137 |
rs185639066 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PWP1 | GRCh38.p7 | 12:107700536 | AAGGCTAAATAATAT[C/T]CCATTGTATGTAATG | 11137 |
rs185786288 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107684071 | GAAACTGTGAGTCCA[C/T]TAAACCTCTTTTTCT | 11137 |
rs185793737 | snp | C/T | 1.65833e-05 | 0.00287948 | intron-variant | PWP1 | GRCh38.p7 | 12:107703070 | GCGGTTCTTAAAAAT[C/T]GGACACAAATATTGG | 11137 |
rs185933492 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PWP1 | GRCh38.p7 | 12:107687541 | GGGAACCACTATTTG[A/G]AGAGTTTATAGGAAA | 11137 |
rs185981253 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107704455 | GTGCCTTCAAGTGTT[A/C]AGATCAGAATCCACC | 11137 |
rs186020560 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | PWP1 | GRCh38.p7 | 12:107698469 | AGGTTGAGGTTGCAG[C/T]GAGCCATGATTGTGT | 11137 |
rs186447723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107702338 | CAGGCTGGAGTCCAG[C/T]GACGTGATCTTGGTT | 11137 |
rs186532348 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PWP1 | GRCh38.p7 | 12:107687946 | TAAGGCAGGAGAATC[A/G]CTTGAACCCGGGAGG | 11137 |
rs186541650 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107690302 | GCAGGATCGCTCAAG[C/T]CCAGGAGTTCAAGGC | 11137 |
rs186550574 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PWP1 | GRCh38.p7 | 12:107709405 | TTTTATGACTTAGAA[C/T]GCTTTGTGGGGAATT | 11137 |
rs186657849 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712550 | TTAAAGCGTAAAATC[C/T]GGTAATATTAAAAGA | 11137 |
rs186668215 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107695038 | AGGCGGGCGGATCAC[A/G]AGTTCAGGAGATCGA | 11137 |
rs186741422 | snp | G/T | 0.0263992 | 0.111815 | intron-variant | PWP1 | GRCh38.p7 | 12:107706902 | TTTTTTGGTTCTATA[G/T]GAACTTTAAAGTAGT | 11137 |
rs186793867 | snp | A/G | 0.00276364 | 0.0370699 | intron-variant | PWP1 | GRCh38.p7 | 12:107699464 | CATTTGAATGATTGT[A/G]AAAGACTGTAGCCAT | 11137 |
rs187406045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107692298 | GTGGAAAAAGCATAC[C/T]GCATTTCTTTTTTCA | 11137 |
rs187419965 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PWP1 | GRCh38.p7 | 12:107705419 | ATACATGTGCACAAC[A/G]TCCAGGTTTGTTACA | 11137 |
rs187518548 | snp | A/C | | | intron-variant | PWP1 | GRCh38.p7 | 12:107700967 | ATTCTTGGGCTCAAG[A/C]AATCCCCCCGCCTCA | 11137 |
rs187526943 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PWP1 | GRCh38.p7 | 12:107708408 | TTTGGCTCTGTATCT[C/G]TCTCTTAATTCCTTC | 11137 |
rs187634452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107705186 | AAAAAAAGTATAAGA[C/T]CTCTGTCTAAATACC | 11137 |
rs187648213 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107711747 | GGTTATTCTGATGTG[C/T]GTGAGTCCTAAGTCC | 11137 |
rs187750753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107700627 | GTGAATAATGCTGCT[A/G]TGAATGTGGGTGTAC | 11137 |
rs188050461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107705142 | GAGAATGCTAACCTG[C/T]TAATTTGTAGCACTA | 11137 |
rs188060932 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107685792 | TGCGCATGCGCTCTG[A/C]CCTGGCAGCGGCCCT | 11137 |
rs188138816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107690019 | ACTGAGCAGGTTAAG[C/T]AAGTTATTTACTTAA | 11137 |
rs188251248 | snp | A/C | 0.0170251 | 0.090679 | intron-variant | PWP1 | GRCh38.p7 | 12:107686205 | CACCCTCAAGCCCAA[A/C]CCCACTCCCAAATTC | 11137 |
rs188407105 | snp | C/T | 0.000155259 | 0.0088094 | intron-variant | PWP1 | GRCh38.p7 | 12:107708890 | TGTTAGATTTTGTGA[C/T]GTAGCATGACCTTGC | 11137 |
rs188552990 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107693987 | TGATCACCTTTCTTA[A/C]TTAAGGAATATTTGT | 11137 |
rs188659449 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107698077 | ATTAAGAACTGCTAG[A/G]CCAGGCCACGCACGT | 11137 |
rs188688223 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107689169 | ATACAGTAGTCCCCC[C/T]TTATCCACGGTTTTG | 11137 |
rs188809974 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PWP1 | GRCh38.p7 | 12:107701419 | CACTTTCTTGGTGCT[A/G]TCATTTGCAGCACAG | 11137 |
rs188923743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107696244 | CATTGTGTTGGCCAG[A/G]CTGGTCTCGAACTCC | 11137 |
rs188924446 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107697337 | TAACATTCAGATGCC[A/G]CATATGCATATAAGT | 11137 |
rs189295716 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | PWP1 | GRCh38.p7 | 12:107702614 | CTGTAAAAAGAAAGA[A/C]AAAAGTCATCAGAGA | 11137 |
rs189296021 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107702218 | GCTATTCTAGGTTCC[C/T]TGCATTTTTAGAATC | 11137 |
rs189437739 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PWP1 | GRCh38.p7 | 12:107687320 | AAATTGTTGGAGGAA[A/G]CAGTTATTAAAAAGA | 11137 |
rs189445686 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107706224 | TCTATTCATATCCTT[C/T]GCCCACTTTTTGATG | 11137 |
rs189468097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107686792 | TAACACGGTGAAACC[C/T]CGTCTCTACTAAAAA | 11137 |
rs189565297 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PWP1 | GRCh38.p7 | 12:107705640 | TTTTCTGTCCTTGCG[A/G]TAGATAGTTTTCTGA | 11137 |
rs189663917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107711635 | TGAGGTAGTCTGGTG[C/T]GTTCTACAAACACAG | 11137 |
rs189680894 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107691962 | AAGCCTTCATTCTTT[A/T]CACTGCATCTTTTCT | 11137 |
rs189687869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107691336 | AAGAAAGACTTAATT[A/G]GGTCCCAGTAAACTT | 11137 |
rs189832956 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107687636 | CCAGTTGCGGTGGCT[A/C]GTGCCTGTAATCCTA | 11137 |
rs189953550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107710122 | GGTTTGTTAGGAAAT[C/T]CCTAAGAGACAGAGT | 11137 |
rs190054580 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PWP1 | GRCh38.p7 | 12:107700550 | TTCCATTGTATGTAA[A/T]GTATGTTACCCGTTC | 11137 |
rs190067821 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107706585 | TTTTGTATAAGCTGT[A/G]AGGAAGGGATCCAGT | 11137 |
rs190167245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107694319 | AAACTTTGAAGATTC[A/G]AAGAGATTATTAGGC | 11137 |
rs190321392 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107699944 | CTGTATGGCTGGGGA[A/G]GCCTCACAGTTATGG | 11137 |
rs190363687 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PWP1 | GRCh38.p7 | 12:107710011 | CCTATTAATAAAAAT[A/G]TAAAAAAGAAAACAA | 11137 |
rs190496186 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PWP1 | GRCh38.p7 | 12:107698789 | GTAAAGACAGAGTTT[C/T]GCTATGTTGCCTGGG | 11137 |
rs190609043 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107685546 | GATTGGTGAAACTTT[A/G]CTTCTGACTGACCCC | 11137 |
rs190632666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107690620 | GGCACATGCCACCAC[A/G]CCCAGCTAATTTTCG | 11137 |
rs190841005 | snp | A/G | 0.000230848 | 0.0107411 | missense | PWP1 | GRCh38.p7 | 12:107704689 | GCCATCGAATGTGGC[A/G]ATTCAGTGGGCAGAT | 11137 |
rs191117491 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PWP1 | GRCh38.p7 | 12:107708044 | GATTAGTAGAGGTGC[A/G]TGCTGTTCTAGCCAG | 11137 |
rs191138861 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107707543 | TGGGTTTGTCATAAA[A/T]AGCTCTTATTATTTT | 11137 |
rs191389641 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PWP1 | GRCh38.p7 | 12:107689408 | TCCCCCGTGGATAAG[C/G]GGGGACTACTGCCTG | 11137 |
rs191458599 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712783 | TTATCAAAGACAAGA[A/G]GCAGACCATTCATTC | 11137 |
rs191474391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107695282 | AAAAAAAAAAAGTTA[C/T]TACCAATTTTATGTA | 11137 |
rs191494454 | snp | C/T | 9.89642e-05 | 0.00703365 | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712230 | TCTTAATGAAGATCA[C/T]CTAATTTCCTGCTTA | 11137 |
rs191510458 | snp | A/C | 0.00438332 | 0.0466095 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107684998 | GCCAAGAGATCAAAA[A/C]CCAGATTTTTCTGGG | 11137 |
rs191614049 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107690171 | TACAAATGTTATCTG[C/T]AACAAAGTAAAATCA | 11137 |
rs191917526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107711778 | GAAAAGTTCTGTGCC[A/G]GTTATGATCAGAGAA | 11137 |
rs192079393 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107708446 | CTTTCTTTCTTGACA[G/T]TGTAACAATGCACTC | 11137 |
rs192251284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107692640 | AAGGTCAAATACAAA[A/G]ATGGCTTTTAAATTC | 11137 |
rs192333423 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107700977 | TCAAGCAATCCCCCC[A/G]CCTCAGCTTCCCAAG | 11137 |
rs192464213 | snp | A/G/T | 0.00319074 | 0.0398324 | upstream-variant-2KB, intron-variant | PWP1 | GRCh38.p7 | 12:107686037 | GGGGTCCGCCCAGCT[A/G/T]GGGGAACGTGGACCC | 11137 |
rs192467464 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107705268 | CTGACATTTCAGTAC[A/C]TGTAAAAAGAAAAGC | 11137 |
rs192505980 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PWP1 | GRCh38.p7 | 12:107687087 | AAACAGTAAAAGGGG[C/T]TGATTTGAATGTACT | 11137 |
rs192523409 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PWP1 | GRCh38.p7 | 12:107709655 | AAACAAATTACTATA[C/T]AGTAGGAAAAATTTA | 11137 |
rs192538547 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | PWP1 | GRCh38.p7 | 12:107690472 | ATAATATACTTTTTT[G/T]TGTGTGTGTGAGACG | 11137 |
rs192643581 | snp | A/T | 0.000132131 | 0.00812699 | intron-variant | PWP1 | GRCh38.p7 | 12:107709066 | ACTTATGATGAAGTA[A/T]ATCTGTATTTCAAAG | 11137 |
rs192729736 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | PWP1 | GRCh38.p7 | 12:107705518 | AATGCTATCCCTCCC[C/G]CTCCCCCCACCCCAC | 11137 |
rs192798244 | snp | C/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107706026 | ACCAACAGTGTAAAA[C/G]TGTTCCTATTTCTCC | 11137 |
rs192868170 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107701450 | GTTTTTCATGTGATG[G/T]TGTCTACTTTATTTC | 11137 |
rs192938639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107686527 | GGAGGATGAGAGGTA[A/G]ATGTCTAACACATGA | 11137 |
rs193111554 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107700784 | CATTTTACATTTTCA[A/C]CAACAATGCACACAA | 11137 |
rs193234346 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107696329 | CGAGCCACTGCGCCC[A/G]GCCTGGAATCTCTTT | 11137 |
rs199535739 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107709535 | TTTTTTTTAAAACCC[C/T]GAAATCAAGACCATC | 11137 |
rs199564672 | snp | C/T | 0.000148284 | 0.00860929 | stop-gained | PWP1 | GRCh38.p7 | 12:107712131 | GAAGCATTTGGAAGA[C/T]GAGAGAGGCTTGTTC | 11137 |
rs199941366 | snp | C/T | | | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107685346 | CTAAATGTTTTTTTC[C/T]CACTTTTTTTTTTGG | 11137 |
rs200035436 | in-del | -/GC | | | intron-variant | PWP1 | GRCh38.p7 | 12:107705864 | TATGCACATACGTGT[-/GC]GCATGTGTCTTTATA | 11137 |
rs200045400 | snp | A/C | | | intron-variant | PWP1 | GRCh38.p7 | 12:107688234 | GTGGAGTAGAATGAG[A/C]ATGATTTTTGAAGTT | 11137 |
rs200093965 | in-del | -/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107693801 | TGGTTTTTTACTCAA[-/T]TTTTTTTTTCTGGCT | 11137 |
rs200118306 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon | PWP1 | GRCh38.p7 | 12:107699390 | TTCCTCAGCAGAAGG[A/G]CATACCGATGCTGTC | 11137 |
rs200160600 | snp | C/T | 0.000396937 | 0.0140823 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107692817 | TTTTTCTTACAGATG[C/T]TGAGACTCTTGGTGA | 11137 |
rs200452351 | snp | A/C/G | 0.000167151 | 0.00914045 | intron-variant | PWP1 | GRCh38.p7 | 12:107710533 | TTTTTAGTTCTCTGC[A/C/G]CACCTCCCCCTGCCC | 11137 |
rs200582334 | snp | C/G | 1.65244e-05 | 0.00287436 | intron-variant | PWP1 | GRCh38.p7 | 12:107710392 | AATCACCATCTTCCT[C/G]TTCTCTCTCTAGGGA | 11137 |
rs200666237 | snp | C/T | 0.000399281 | 0.0141238 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107696498 | AAGAAGAAGACTCTT[C/T]TTATGTACACCATGA | 11137 |
rs200668964 | snp | C/T | 0.00199792 | 0.0315431 | intron-variant | PWP1 | GRCh38.p7 | 12:107703767 | AAAGCACAGCAAGAA[C/T]GATTGCTACTCTGTT | 11137 |
rs200716071 | snp | A/C | | | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107685348 | AAATGTTTTTTTCTC[A/C]CTTTTTTTTTTGGTG | 11137 |
rs200797884 | in-del | -/TAG | 0.00993419 | 0.0697739 | intron-variant | PWP1 | GRCh38.p7 | 12:107704808 | ACTTTTTAAATTCCA[-/TAG]TAGAGAGAATTATCT | 11137 |
rs200812557 | snp | A/G | | | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107683894 | CCTCGGCCTCCCAAA[A/G]TGCTGGGATTACAGG | 11137 |
rs200835776 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107685428 | AATGGTGGGATCTCC[A/G]TGAAACGACAAATTC | 11137 |
rs200858006 | in-del | -/A | 0.0182019 | 0.0936463 | intron-variant | PWP1 | GRCh38.p7 | 12:107709814 | ATATAAATATAATGG[-/A]AAAACAGGTTACAGA | 11137 |
rs201011242 | in-del | -/A | | | intron-variant | PWP1 | GRCh38.p7 | 12:107709528 | TTTTTTTTTTTTTTT[-/A]AAACCCTGAAATCAA | 11137 |
rs201034471 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107710359 | GATCTAGATATTAGC[A/G]CTTTCTGAAGAGATT | 11137 |
rs201078652 | snp | C/T | 9.96545e-05 | 0.00705814 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107688740 | CAGAGGATGACAGGA[C/T]GCTTGATGATGATGA | 11137 |
rs201124969 | snp | A/G | 0.000182805 | 0.00955871 | upstream-variant-2KB, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107685856 | TCGTGGTCCCTCCCT[A/G]TGCAGCCTGGTTTCT | 11137 |
rs201193016 | snp | C/T | 1.65195e-05 | 0.00287393 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107692825 | ACAGATGCTGAGACT[C/T]TTGGTGAATCTCTCT | 11137 |
rs201201962 | snp | C/T | 0.000362755 | 0.0134628 | intron-variant | PWP1 | GRCh38.p7 | 12:107703658 | CAAACCAACAGAGAT[C/T]TCTGCATTTATGTTT | 11137 |
rs201234714 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107688290 | AAGAATCTATAAAAT[C/T]TATATTTTTTAATAT | 11137 |
rs201403302 | snp | A/G | 4.9588e-05 | 0.00497911 | missense | PWP1 | GRCh38.p7 | 12:107708992 | CCAATTTTTACACTT[A/G]ATGCACACAATGATG | 11137 |
rs201555390 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107697039 | TAGTTGCCCCTGTCC[A/G]TACTTTTTAATAAAG | 11137 |
rs201646899 | in-del | -/A | 0.00755907 | 0.0610114 | intron-variant | PWP1 | GRCh38.p7 | 12:107689005 | ACAAATCTAGGATCT[-/A]AAAAAAAAAGTACTG | 11137 |
rs201740995 | snp | A/G/T | 0.000512459 | 0.0160005 | intron-variant | PWP1 | GRCh38.p7 | 12:107703042 | ACAAGGTATGGTGAT[A/G/T]TAGTTGATCACAGCG | 11137 |
rs201788507 | snp | A/G | 0.000399281 | 0.0141238 | missense | PWP1 | GRCh38.p7 | 12:107710406 | TGTTCTCTCTCTAGG[A/G]AGTTCTCTTCTGTTC | 11137 |
rs201835232 | snp | C/T | 0.000164959 | 0.00908033 | missense | PWP1 | GRCh38.p7 | 12:107704730 | ACTTGGAATCACTTT[C/T]CACCTTGTCATTTCT | 11137 |
rs201999166 | snp | A/C | | | intron-variant | PWP1 | GRCh38.p7 | 12:107688030 | AGCGAGACTCCGTCT[A/C]AAAAAAAAAAAAAAA | 11137 |
rs202018856 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107706640 | CAGTTTTCCCAGCAC[C/T]ATTTATTAAATAGGG | 11137 |
rs202133075 | snp | C/G | 4.9525e-05 | 0.00497595 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107688698 | GCACCCAGGCACGCC[C/G]AAGAGAGCCCCTGGA | 11137 |
rs202149257 | snp | C/T | 1.65004e-05 | 0.00287227 | stop-gained | PWP1 | GRCh38.p7 | 12:107704658 | GCTTTGTATGACTGC[C/T]GAAGTCCAGATGAAA | 11137 |
rs202155195 | snp | C/G/T | 6.60299e-05 | 0.00574554 | intron-variant | PWP1 | GRCh38.p7 | 12:107709082 | ATCTGTATTTCAAAG[C/G/T]GAAAGTGTCTAAACT | 11137 |
rs202156889 | snp | C/T | 0.000280364 | 0.0118365 | utr-variant-5-prime, synonymous-codon | PWP1 | GRCh38.p7 | 12:107688624 | TCATAGAGAAGAAGG[C/T]GGTGGCAGTGATGAA | 11137 |
rs202246559 | in-del | -/T | 0.00318978 | 0.0398085 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107685685 | GATTCCTCGCCCGGC[-/T]GCTTCCGCTTCCATT | 11137 |
rs367624813 | snp | C/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107700070 | CTTGTGAGACCCATT[C/G]ACTATCATGAGAACA | 11137 |
rs367676453 | snp | C/T | 3.29853e-05 | 0.00406098 | intron-variant | PWP1 | GRCh38.p7 | 12:107712103 | TTACCTGTTTATTTG[C/T]ATTTTAGTAAATGAA | 11137 |
rs367798858 | snp | C/T | 0.000164861 | 0.00907764 | synonymous-codon | PWP1 | GRCh38.p7 | 12:107709169 | TTCAGCTGACAAATA[C/T]GTGAAGATCTGGGAC | 11137 |
rs367893668 | snp | C/T | 3.30022e-05 | 0.00406202 | intron-variant | PWP1 | GRCh38.p7 | 12:107709100 | AAGTGTCTAAACTTA[C/T]CTTCCTTTAGGTCTT | 11137 |
rs368137274 | snp | A/C | 0.000186168 | 0.0096462 | intron-variant | PWP1 | GRCh38.p7 | 12:107697868 | AGCTACTATAGATGA[A/C]GGACTTTCGGATTAT | 11137 |
rs368140510 | snp | C/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107688132 | GAGAGGTGCCCTAGA[C/G]AGAGTCAGAGATGGT | 11137 |
rs368353871 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | PWP1 | GRCh38.p7 | 12:107709057 | TTTTTCTTAACTTAT[A/G]ATGAAGTAAATCTGT | 11137 |
rs368386164 | snp | C/T | 0.000153988 | 0.00877328 | utr-variant-5-prime, synonymous-codon | PWP1 | GRCh38.p7 | 12:107688459 | ACAGGTAGAGCTGAG[C/T]AAAGAAGAAGTAAAA | 11137 |
rs368506876 | snp | C/T | 6.77243e-05 | 0.00581873 | intron-variant | PWP1 | GRCh38.p7 | 12:107704596 | AAACATATAGGAGAA[C/T]TGAACTCTTAAAACC | 11137 |
rs368520206 | snp | A/G | 3.38163e-05 | 0.00411182 | upstream-variant-2KB, intron-variant | PWP1 | GRCh38.p7 | 12:107686015 | GAGCAGCGTCTTTAC[A/G]GCACTGGGGGTCCGC | 11137 |
rs368636928 | in-del | -/C | | | intron-variant | PWP1 | GRCh38.p7 | 12:107689169 | TACAGTAGTCCCCCC[-/C]TTATCCACGGTTTTG | 11137 |
rs368653527 | snp | A/C | 0.000153988 | 0.00877328 | intron-variant | PWP1 | GRCh38.p7 | 12:107697609 | GAAGGTAAAGAAGTT[A/C]ATAAATATTTAAACT | 11137 |
rs368685405 | in-del | -/ATAT | 0.00597247 | 0.0543191 | intron-variant | PWP1 | GRCh38.p7 | 12:107711656 | ACAAACACAGAGATA[-/ATAT]ATATATCTCCCCACT | 11137 |
rs368748715 | snp | A/C/G | 1.6476e-05 | 0.00287014 | missense | PWP1 | GRCh38.p7 | 12:107712132 | AAGCATTTGGAAGAC[A/C/G]AGAGAGGCTTGTTCT | 11137 |
rs368852868 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107686782 | GCATCCTGGCTAACA[C/T]GGTGAAACCCCGTCT | 11137 |
rs368963299 | snp | C/T | 1.74433e-05 | 0.0029532 | intron-variant | PWP1 | GRCh38.p7 | 12:107697429 | AGTTCTGTATGTCTT[C/T]TTTTGTGTAATCATA | 11137 |
rs369216348 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107698367 | GTCTCAAGGGAAAAA[A/G]AAGAACTGCTAGGCC | 11137 |
rs369227507 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107706963 | TAGCTTGATGGGGAT[A/G]GCATTGAATCTACAA | 11137 |
rs369257884 | snp | C/T | 0.000131857 | 0.00811855 | missense | PWP1 | GRCh38.p7 | 12:107712206 | AGGAGCTCAGATACA[C/T]CCATGGAGTCTTAAT | 11137 |
rs369268683 | snp | A/C | 3.3095e-05 | 0.00406773 | intron-variant | PWP1 | GRCh38.p7 | 12:107692960 | AAAACCTTACTGGCT[A/C]TCTGCTTCTAGTCAA | 11137 |
rs369287197 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107691463 | AGGAAGTTAACTCTG[G/T]CAACAGTGGAGAACA | 11137 |
rs369503318 | snp | C/T | 1.65233e-05 | 0.00287426 | intron-variant | PWP1 | GRCh38.p7 | 12:107709056 | ATTTTTCTTAACTTA[C/T]GATGAAGTAAATCTG | 11137 |
rs369564899 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | PWP1 | GRCh38.p7 | 12:107688571 | TGGTCTTGTTATTAG[A/G]AGGTAGCATTTGGGT | 11137 |
rs369595409 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107710934 | GCCGAGACCAGCTCG[A/G]TTGGGGAGACCCTAA | 11137 |
rs369703711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107687754 | ATTAAAATTAAGGCC[A/G]GGCACGGTGGCTCAC | 11137 |
rs369751704 | snp | A/C/G | 0.00159649 | 0.0282165 | intron-variant | PWP1 | GRCh38.p7 | 12:107697283 | GTGACCTAGTTAGAA[A/C/G]TGCCCACCCAGAACC | 11137 |
rs369762876 | snp | A/G | 0.000153988 | 0.00877328 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107688755 | CGCTTGATGATGATG[A/G]GCTGGCTGAGTACGA | 11137 |
rs369817857 | snp | C/T | 1.64936e-05 | 0.00287168 | synonymous-codon | PWP1 | GRCh38.p7 | 12:107704675 | AAGTCCAGATGAAAG[C/T]CATCGAATGTGGCGA | 11137 |
rs369933570 | snp | C/T | 3.32679e-05 | 0.00407834 | intron-variant | PWP1 | GRCh38.p7 | 12:107710358 | GGATCTAGATATTAG[C/T]GCTTTCTGAAGAGAT | 11137 |
rs369963999 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107711305 | TTCCTTGCCCTCATT[C/T]GTAAACCCACAACCT | 11137 |
rs370002015 | snp | A/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107701822 | AGCTGGGATTACTGG[A/T]GCATGCCACCATGCC | 11137 |
rs370019322 | snp | G/T | 0.000347013 | 0.0131676 | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712255 | TGCTTACCTTAACTG[G/T]GAATTTTAAAAAGTT | 11137 |
rs370072718 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PWP1 | GRCh38.p7 | 12:107687902 | TGGGCGTGGTGGCGC[A/G]TGCCTGTAATCCCAG | 11137 |
rs370079515 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107707489 | CAGTTTTCAAAGGGA[A/G]TGCTTCCAGTTTTTG | 11137 |
rs370131698 | snp | A/C/T | 3.32338e-05 | 0.00407627 | upstream-variant-2KB, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107685862 | TCCCTCCCTATGCAG[A/C/T]CTGGTTTCTAGCGTG | 11137 |
rs370184368 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PWP1 | GRCh38.p7 | 12:107699505 | CCTCATGCCTACACT[C/G]ATCTCTTTATTTGTG | 11137 |
rs370249789 | snp | A/G | 0.00128624 | 0.0253271 | missense | PWP1 | GRCh38.p7 | 12:107703014 | CCAGCAGCTAGCCTC[A/G]CTGTACACACAGACA | 11137 |
rs370290059 | snp | A/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107688289 | TAAGAATCTATAAAA[A/T]CTATATTTTTTAATA | 11137 |
rs370334930 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107700120 | CCATGATTCCATTAC[C/T]TTCCACCTGGTCCTT | 11137 |
rs370344046 | snp | G/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107704000 | TTGCCTTTATGGGAA[G/T]AATTTCCATGTCACA | 11137 |
rs370381325 | snp | C/G/T | 0.00279162 | 0.0372561 | intron-variant | PWP1 | GRCh38.p7 | 12:107693346 | ATAGGGGTGTTTTTT[C/G/T]TTGTTTTTATATATA | 11137 |
rs370430034 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | PWP1 | GRCh38.p7 | 12:107697034 | ACTATTAGTTGCCCC[-/T]GTCCGTACTTTTTAA | 11137 |
rs370557814 | snp | A/G | 0.000584815 | 0.0170899 | intron-variant | PWP1 | GRCh38.p7 | 12:107708891 | GTTAGATTTTGTGAC[A/G]TAGCATGACCTTGCC | 11137 |
rs370580980 | snp | A/C | 1.66034e-05 | 0.00288122 | intron-variant | PWP1 | GRCh38.p7 | 12:107710536 | TTAGTTCTCTGCACA[A/C]CTCCCCCTGCCCCTG | 11137 |
rs370694404 | snp | G/T | 1.64779e-05 | 0.00287031 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107696550 | TCTGAGTGTGGAATG[G/T]CTGAATTTTGATCCT | 11137 |
rs370738504 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PWP1 | GRCh38.p7 | 12:107705355 | AAATATGTAGTGCTT[C/T]GCAAAGGTGAGAAAG | 11137 |
rs370910879 | snp | G/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107688399 | TTTAATTCAAATAAT[G/T]TGATGATTTCCTTAC | 11137 |
rs370912288 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PWP1 | GRCh38.p7 | 12:107693649 | GGTGGGAGGATTGCT[C/T]GAGCCCATGAGTTCT | 11137 |
rs370940977 | snp | A/G | 0.000313609 | 0.0125182 | intron-variant | PWP1 | GRCh38.p7 | 12:107709083 | TCTGTATTTCAAAGC[A/G]AAAGTGTCTAAACTT | 11137 |
rs370983395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107699253 | AACAGACAAAGACTC[C/T]GTCTCAAAACAAAAC | 11137 |
rs370984713 | snp | C/T | 8.26973e-05 | 0.00642976 | missense | PWP1 | GRCh38.p7 | 12:107708963 | TATATAATTTGGATG[C/T]ACGTTCAGATAAGCC | 11137 |
rs371101822 | snp | A/C | 0.000307953 | 0.0124049 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107696495 | ATCAAGAAGAAGACT[A/C]TTTTTATGTACACCA | 11137 |
rs371141736 | in-del | -/TAT | | | intron-variant | PWP1 | GRCh38.p7 | 12:107691678 | TGGTTTCCATCTTAT[-/TAT]CGCTGGTGTACCTCT | 11137 |
rs371508932 | snp | C/T | 1.64923e-05 | 0.00287156 | utr-variant-5-prime, missense | PWP1 | GRCh38.p7 | 12:107688656 | AGGAGACAGGCAGTC[C/T]TTCAGAAGATGGCAT | 11137 |
rs371565762 | snp | C/T | 0.000193981 | 0.00984647 | intron-variant | PWP1 | GRCh38.p7 | 12:107708874 | TAGACTTTTTACCCA[C/T]TGTTAGATTTTGTGA | 11137 |
rs371625529 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107703316 | GGTCTGTCAGTCACA[A/G]TGGTAACACCCATTA | 11137 |
rs371641978 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107694267 | AGTCCATCCTTGCCC[A/G]ATACTCTCCTCCCCC | 11137 |
rs371723969 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PWP1 | GRCh38.p7 | 12:107710651 | CCTCAGCCTTCTGTA[C/T]AGCTGGGATTACAGG | 11137 |
rs371811595 | snp | C/T | 4.95602e-05 | 0.00497771 | synonymous-codon | PWP1 | GRCh38.p7 | 12:107699396 | AGCAGAAGGGCATAC[C/T]GATGCTGTCCTTGAC | 11137 |
rs371877269 | snp | G/T | 0.00192415 | 0.0309576 | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712272 | AATTTTAAAAAGTTG[G/T]CCTAAAAATGTTCCA | 11137 |
rs371892765 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107696954 | AACATAAGCTAAAAC[C/T]GAAATGAAGAGGCTT | 11137 |
rs371942426 | snp | C/T | | | upstream-variant-2KB, intron-variant | PWP1 | GRCh38.p7 | 12:107686032 | CACTGGGGGTCCGCC[C/T]AGCTGGGGGAACGTG | 11137 |
rs371970371 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107706118 | GATGGTATCTCATTG[C/T]GGTTTTGATTTGCAT | 11137 |
rs372119910 | snp | C/T | 6.59772e-05 | 0.00574319 | stop-gained | PWP1 | GRCh38.p7 | 12:107709128 | CTTGATCTTAGCAGT[C/T]AAATCAAGGGCTGTC | 11137 |
rs372202257 | snp | A/G/T | 3.31155e-05 | 0.00406901 | intron-variant | PWP1 | GRCh38.p7 | 12:107699454 | AAAGAAATAACATTT[A/G/T]AATGATTGTAAAAGA | 11137 |
rs372243352 | snp | C/T | 4.96866e-05 | 0.00498406 | synonymous-codon | PWP1 | GRCh38.p7 | 12:107697561 | CTTCACACTCGGAAG[C/T]AAACTTTCAAAAAAG | 11137 |
rs372386065 | snp | G/T | 0.000153988 | 0.00877328 | missense | PWP1 | GRCh38.p7 | 12:107712167 | AGTGCAAGAAATTCA[G/T]CTATTAGTGGCCCTT | 11137 |
rs372409589 | in-del | -/TT | | | intron-variant | PWP1 | GRCh38.p7 | 12:107692117 | TTCAGAATCAGCTCT[-/TT]CTCGTGTAGCAGAAA | 11137 |
rs372443242 | snp | A/G | 3.43083e-05 | 0.00414161 | intron-variant | PWP1 | GRCh38.p7 | 12:107708894 | AGATTTTGTGACGTA[A/G]CATGACCTTGCCCAT | 11137 |
rs372506141 | snp | A/G | 0.000148661 | 0.00862023 | intron-variant, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107692975 | CTCTGCTTCTAGTCA[A/G]TGACATTTTTTTCCT | 11137 |
rs372556525 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107696029 | TCATGATATTGGAAT[C/T]TTTTTTTTTTTTTTT | 11137 |
rs372572732 | snp | A/G | 4.95168e-05 | 0.00497553 | intron-variant | PWP1 | GRCh38.p7 | 12:107688532 | GACCAGATGAAATCT[A/G]TATCTTAAATGATGA | 11137 |
rs372707274 | snp | C/T | 1.65312e-05 | 0.00287495 | intron-variant | PWP1 | GRCh38.p7 | 12:107709246 | TGGTAAGAATCTCCC[C/T]GGGTATCTGTTTTTT | 11137 |
rs372914792 | snp | G/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107711741 | TCTCTGGGTTATTCT[G/T]ATGTGTGTGAGTCCT | 11137 |
rs373155062 | snp | C/T | 8.26904e-05 | 0.00642949 | intron-variant | PWP1 | GRCh38.p7 | 12:107704757 | TTCTTGGTAAGAGTA[C/T]GAATGTTGTTGTTTT | 11137 |
rs373224470 | snp | A/G/T | 0.000134844 | 0.00820997 | intron-variant | PWP1 | GRCh38.p7 | 12:107710551 | CCTCCCCCTGCCCCT[A/G/T]TAAAAAAAAAAAAAA | 11137 |
rs373377717 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107689895 | GGAAAGTAGGTATAA[C/T]GATAAATGGAAAAGG | 11137 |
rs373380067 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PWP1 | GRCh38.p7 | 12:107710177 | TGGTCAGAAGTTGCA[A/G]ATATCATTGTGGAAG | 11137 |
rs373413931 | snp | A/G | 0.000153988 | 0.00877328 | missense | PWP1 | GRCh38.p7 | 12:107702937 | TTCCCTTTCTCAGAA[A/G]TGTTTTAGCAAGTGC | 11137 |
rs373564146 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107694549 | TGTGATCTGTTTATG[C/T]ATAGCAGGCACTTTA | 11137 |
rs373586949 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PWP1 | GRCh38.p7 | 12:107708075 | GCAGCCTGAAGCCTG[A/C]CTTATTTTTACAATG | 11137 |
rs373604479 | snp | A/C/T | 5.17811e-05 | 0.00508806 | intron-variant | PWP1 | GRCh38.p7 | 12:107697451 | GTAATCATACATGCA[A/C/T]TGTTTCCTCCCATAG | 11137 |
rs373714204 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107683882 | GTAATCCAACTGCCT[C/T]GGCCTCCCAAAGTGC | 11137 |
rs373765288 | snp | A/G | 4.95446e-05 | 0.00497693 | missense | PWP1 | GRCh38.p7 | 12:107703027 | TCGCTGTACACACAG[A/G]CAAGGTATGGTGATT | 11137 |
rs373824813 | snp | C/T | 5.04876e-05 | 0.00502407 | upstream-variant-2KB, intron-variant | PWP1 | GRCh38.p7 | 12:107686011 | AGGGGAGCAGCGTCT[C/T]TACGGCACTGGGGGT | 11137 |
rs374029100 | snp | A/G | 8.60904e-05 | 0.00656032 | intron-variant | PWP1 | GRCh38.p7 | 12:107693134 | AAAGATTTTCTAAGT[A/G]ATGGTAAAATAATAA | 11137 |
rs374143760 | snp | A/T | 1.80175e-05 | 0.00300141 | intron-variant | PWP1 | GRCh38.p7 | 12:107688412 | ATTTGATGATTTCCT[A/T]ACACATATTGTAATG | 11137 |
rs374222545 | snp | A/G | 0.000264905 | 0.0115058 | intron-variant | PWP1 | GRCh38.p7 | 12:107703057 | TTAGTTGATCACAGC[A/G]GTTCTTAAAAATCGG | 11137 |
rs374377403 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107686762 | ACGAGGTCAGGAGAT[C/G/T]GAGAGCATCCTGGCT | 11137 |
rs374512923 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107711848 | AAGGCCAGGAGAGGG[C/T]CACTTATAAGGAATG | 11137 |
rs374624364 | snp | C/T | 1.65277e-05 | 0.00287464 | synonymous-codon | PWP1 | GRCh38.p7 | 12:107709015 | CAATGATGAAATCTC[C/T]GGTGAGCAAGAGTAA | 11137 |
rs374816430 | snp | A/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107693432 | CTGATTTGGCCTCCC[A/T]AAGTGCTGGGTGCTG | 11137 |
rs374819828 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PWP1 | GRCh38.p7 | 12:107698269 | TGGGAGGCTGAGGCA[A/G]GAGAATCACTTGAAC | 11137 |
rs374890386 | snp | C/T | 0.000132512 | 0.00813869 | intron-variant | PWP1 | GRCh38.p7 | 12:107699460 | ATAACATTTGAATGA[C/T]TGTAAAAGACTGTAG | 11137 |
rs374907666 | snp | C/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107699258 | ACAAAGACTCCGTCT[C/G]AAAACAAAACAAAAC | 11137 |
rs375085155 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107691799 | CATTCCTCCGTTTTC[C/T]TCATTCGCTTGGCCA | 11137 |
rs375086152 | snp | C/T | | | synonymous-codon | PWP1 | GRCh38.p7 | 12:107710485 | AGAAGGGCTTCGGGT[C/T]TGGGATATAAGCACA | 11137 |
rs375200694 | snp | A/G | 0.000495426 | 0.0157311 | missense | PWP1 | GRCh38.p7 | 12:107699397 | GCAGAAGGGCATACC[A/G]ATGCTGTCCTTGACC | 11137 |
rs375244271 | snp | G/T | 0.000511387 | 0.0159822 | intron-variant | PWP1 | GRCh38.p7 | 12:107688548 | TATCTTAAATGATGA[G/T]GACCATGTGGTCTTG | 11137 |
rs375263543 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107697254 | CCAGCAGCAGCACAG[C/T]ATGGTTATCACCTGT | 11137 |
rs375618812 | snp | A/T | 6.59914e-05 | 0.00574381 | synonymous-codon | PWP1 | GRCh38.p7 | 12:107710407 | GTTCTCTCTCTAGGG[A/T]GTTCTCTTCTGTTCT | 11137 |
rs375625096 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107687900 | GCTGGGCGTGGTGGC[A/G]CGTGCCTGTAATCCC | 11137 |
rs375631230 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PWP1 | GRCh38.p7 | 12:107707418 | GATTGCCCTGGCCAG[A/G]ACTTCCAACACTGTG | 11137 |
rs375671620 | snp | C/T | 6.59239e-05 | 0.00574087 | synonymous-codon, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107696502 | AGAAGACTCTTTTTA[C/T]GTACACCATGATATA | 11137 |
rs375698016 | snp | C/T | 1.65853e-05 | 0.00287964 | synonymous-codon | PWP1 | GRCh38.p7 | 12:107697567 | ACTCGGAAGTAAACT[C/T]TCAAAAAAGAAGAAA | 11137 |
rs375712614 | snp | C/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107703900 | CTTTTAACTCTGGTC[C/G]TTTCAGTCTACAACG | 11137 |
rs375758061 | snp | C/T | 8.28521e-05 | 0.00643577 | synonymous-codon | PWP1 | GRCh38.p7 | 12:107708940 | GGCCAGTACAGATGA[C/T]GGCTTTGTATATAAT | 11137 |
rs375799398 | snp | C/T | 0.000437904 | 0.0147905 | intron-variant | PWP1 | GRCh38.p7 | 12:107699501 | CTTACCTCATGCCTA[C/T]ACTCATCTCTTTATT | 11137 |
rs375959266 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107691212 | GCTTGACCTGATGTA[C/T]GTGATGATACAGCCT | 11137 |
rs376169189 | snp | C/T | 8.24885e-05 | 0.00642164 | synonymous-codon | PWP1 | GRCh38.p7 | 12:107703013 | ACCAGCAGCTAGCCT[C/T]GCTGTACACACAGAC | 11137 |
rs376241508 | snp | A/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107710552 | CTCCCCCTGCCCCTG[A/T]AAAAAAAAAAAAAAA | 11137 |
rs376243882 | snp | A/T | 0.000153988 | 0.00877328 | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712232 | TTAATGAAGATCATC[A/T]AATTTCCTGCTTACC | 11137 |
rs376285721 | snp | C/G | 8.24097e-05 | 0.00641857 | synonymous-codon | PWP1 | GRCh38.p7 | 12:107703687 | TTCCTCCCTTTAGGT[C/G]CAAACACTGCAGTTT | 11137 |
rs376343301 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107710921 | TAGATCATTTAAGGC[C/T]GAGACCAGCTCGGTT | 11137 |
rs376393772 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PWP1 | GRCh38.p7 | 12:107686767 | GTCAGGAGATCGAGA[C/G]CATCCTGGCTAACAC | 11137 |
rs376432685 | in-del | -/CACT | | | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107685301 | TTGCCAAGACTAAAT[-/CACT]ACTGCATAGTTAGTA | 11137 |
rs376470703 | snp | C/G | 1.64882e-05 | 0.00287121 | missense | PWP1 | GRCh38.p7 | 12:107709159 | TCGTGACTGCTTCAG[C/G]TGACAAATACGTGAA | 11137 |
rs376542301 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107711883 | ATTTGTTACCAAGGC[A/G]GATCAGATAAATCCA | 11137 |
rs376608975 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107686480 | ATAGGGAATTTCTTG[C/T]AGTAATCCAAGTGAG | 11137 |
rs376651607 | snp | C/T | | | upstream-variant-2KB, intron-variant | PWP1 | GRCh38.p7 | 12:107686031 | GCACTGGGGGTCCGC[C/T]CAGCTGGGGGAACGT | 11137 |
rs376706240 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107701967 | ATAGGCATGAGCCAC[C/T]GCGCCCAGCCCCATT | 11137 |
rs376924188 | snp | G/T | | | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107684485 | TGGTCTTTCTAAAAT[G/T]GGTTAAAAGCAAAGA | 11137 |
rs376988632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107693208 | TATCTCATTTAAGTT[A/G]GTTACATAGTTAACT | 11137 |
rs376991812 | in-del | -/AGTA | 0.00335037 | 0.0407917 | intron-variant | PWP1 | GRCh38.p7 | 12:107692903 | CTGAAAGATACAGTA[-/AGTA]TTTACATCTTTTTTC | 11137 |
rs377035123 | snp | A/G | 0.000153988 | 0.00877328 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107693061 | TTATAGTTTGTGGCC[A/G]AGCTGAACAGGACCA | 11137 |
rs377040884 | snp | C/T | 1.65097e-05 | 0.00287308 | synonymous-codon | PWP1 | GRCh38.p7 | 12:107704744 | TTCACCTTGTCATTT[C/T]TTGGTAAGAGTACGA | 11137 |
rs377062294 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107702366 | GTTCTCTGCAACCTC[C/T]GCTTTTTGGGTTCAA | 11137 |
rs377168923 | snp | C/T | 0.000465704 | 0.0152524 | intron-variant | PWP1 | GRCh38.p7 | 12:107709282 | TTCTGTTTCTGACCT[C/T]GTCTTTTTCTGGAAC | 11137 |
rs377255136 | snp | C/T | 0.000153988 | 0.00877328 | upstream-variant-2KB, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107685859 | TGGTCCCTCCCTATG[C/T]AGCCTGGTTTCTAGC | 11137 |
rs377416936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107687709 | AGTTCACAGCTGCAG[A/G]GAGCTGTGACCATGC | 11137 |
rs377443318 | snp | G/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107687035 | TATGGAGTCGACATG[G/T]GCACATATAGTATGT | 11137 |
rs377490385 | snp | A/G | 0.000153988 | 0.00877328 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107696531 | TACTCTTGTCTGCAT[A/G]TCCTCTGAGTGTGGA | 11137 |
rs377533535 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107698493 | ATTGTGTGCCACTGC[A/G]CTCCAACCTGGGTGA | 11137 |
rs377562217 | snp | C/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107700988 | CCCCGCCTCAGCTTC[C/G]CAAGTCACTTGGAGT | 11137 |
rs377623895 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PWP1 | GRCh38.p7 | 12:107693462 | GGATTACAGGTGTGA[A/G]CCACCACACCTGGCC | 11137 |
rs377626641 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PWP1 | GRCh38.p7 | 12:107711985 | CATTAACTTGGACTT[C/T]TGAGTTGGTTACTCA | 11137 |
rs377638908 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | PWP1 | GRCh38.p7 | 12:107696463 | AAAGTCTCTTTTCCC[A/G]ATCTTTTCAGTTTAT | 11137 |
rs377650384 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107699127 | AGCTGGGCATGGTGG[C/T]ATGCGCGTGTAATCC | 11137 |
rs397700499 | in-del | -/TT | 0.5 | 0 | intron-variant | PWP1 | GRCh38.p7 | 12:107696050 | TTTTTTTTTTTTTTT[-/TT]GAGATAGAGTCTCAC | 11137 |
rs397719370 | in-del | -/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107709527 | TTTTTTTTTTTTTTT[-/T]AAAACCCTGAAATCA | 11137 |
rs398020976 | in-del | -/C | 0 | 0 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107684374 | TCCTCCATCAAAGCA[-/C]CCCCCCCCCGCCCCC | 11137 |
rs398020977 | in-del | -/G | 0 | 0 | intron-variant | PWP1 | GRCh38.p7 | 12:107700904 | CTTACCTTAAAAAAA[-/G]GGGGGGGAAATGCAA | 11137 |
rs398044794 | in-del | -/T | 0.5 | 0 | intron-variant | PWP1 | GRCh38.p7 | 12:107702252 | TGTCACTTTTTTTTT[-/T]AAGTCTAATACTAAT | 11137 |
rs527351164 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PWP1 | GRCh38.p7 | 12:107704339 | CCAGAGAAGGGGAAA[A/T]TAGAAATTGTCCTGG | 11137 |
rs527366185 | snp | C/T | 1.65277e-05 | 0.00287464 | missense | PWP1 | GRCh38.p7 | 12:107697553 | GAGCCAGTCTTCACA[C/T]TCGGAAGTAAACTTT | 11137 |
rs527476061 | snp | G/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107692434 | ATTTATTATGTTGAT[G/T]TCAGTGTTTCAGGGT | 11137 |
rs527688049 | in-del | -/A | | | intron-variant | PWP1 | GRCh38.p7 | 12:107689004 | ACAAATCTAGGATCT[-/A]AAAAAAAAAAGTACT | 11137 |
rs527735903 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PWP1 | GRCh38.p7 | 12:107703582 | TGTATTTCAGAGGGA[C/T]GCATTTATAGAAATA | 11137 |
rs527835354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107696415 | TGTTTTTTTGAGCGG[A/G]ATGTGATTTTTGATG | 11137 |
rs527952226 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107702410 | CTCAGCCTCCTGAGT[A/T]ACTGGGATTACAGGC | 11137 |
rs527986085 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107701921 | GACCTCAAGTGATCT[G/T]CCTGCCTCTGCCTTG | 11137 |
rs527988132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107708521 | CTGCCACACTGGTCG[A/G]TTTGACTGTTGGTCA | 11137 |
rs528073340 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107707899 | GGCTTTGGTATCAGG[A/G]TGATGCTGGCCTCAT | 11137 |
rs528257938 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107704908 | TTTTAAATAAGAGAA[C/T]GGCTCTTACTTAAAA | 11137 |
rs528293549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107688270 | TAGCGAGAGATCTTA[C/T]TTGTAAGAATCTATA | 11137 |
rs528330584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107687767 | CCGGGCACGGTGGCT[C/T]ACGCCTGTAATCCCA | 11137 |
rs528463369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107701076 | GAGCATCTTTGTTTT[A/G]TGCTTATTGGCCATT | 11137 |
rs528474468 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107693568 | CCTGGAAGTAAAATT[A/C]TATATAAAAATACAA | 11137 |
rs528516295 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107699993 | CAAAGTCATGTCTTA[C/T]ATAGTGGCAGGCAGG | 11137 |
rs528557599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107700589 | GTGGTCACCTGGATT[A/G]CTTCTTCTGCCTTTT | 11137 |
rs528687463 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712623 | TGCACAGGAGGCCAT[A/G]AACAGAGGCAAGTGC | 11137 |
rs528837737 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107702486 | GTTTCACCATGTTGG[C/G]CAGGCTGGTCTTGAA | 11137 |
rs529219275 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107688357 | CATTGCTTGGCGTTA[C/T]ATTTTACATTTGTTT | 11137 |
rs529224876 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107700709 | TATTACTGAATCTTA[C/T]GGTAATTCTATTTTT | 11137 |
rs529304041 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107687867 | TGAAACCCAGTCTCT[A/G]CCAAAATACAAAAAT | 11137 |
rs529360654 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107694263 | GACAAGTCCATCCTT[A/G]CCCGATACTCTCCTC | 11137 |
rs529377009 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107701714 | GACAGGGTCTTACTC[A/T]GTCACCCAGGCTAGA | 11137 |
rs529447337 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PWP1 | GRCh38.p7 | 12:107706782 | TTTGGTACCAGTACC[A/G]TGCTGTTTTGGTTAC | 11137 |
rs529513080 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | PWP1 | GRCh38.p7 | 12:107695324 | GAGTATATCGAACAT[-/G]GTTGAGGTTTTTGTA | 11137 |
rs529713615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107687042 | TCGACATGTGCACAT[A/G]TAGTATGTCAGTGGG | 11137 |
rs529795493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107693335 | GGAAATTTTTCATAG[A/G]GGTGTTTTTTTTTGT | 11137 |
rs529827834 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107706082 | CTGACTTTTTAATGA[C/T]CGCCATTCTAACTGG | 11137 |
rs529946153 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107705521 | GCTATCCCTCCCCCT[A/C]CCCCCACCCCACGAC | 11137 |
rs529946390 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107699075 | ACCACCCTGGCCAAC[A/G]TGGCAAAACCCTGTC | 11137 |
rs530033908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107711784 | TTCTGTGCCGGTTAT[A/G]ATCAGAGAAAAGTGA | 11137 |
rs530138529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107711220 | TAAGACACAGATCGA[A/G]ATCGCTCATGCTATT | 11137 |
rs530246074 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107692316 | ATTTCTTTTTTCATA[C/T]GCCAATAAGGCATAT | 11137 |
rs530291793 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107685320 | ACTGCATAGTTAGTA[C/T]ATAATTGGTGCTAAA | 11137 |
rs530468207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107691399 | TGTGCGAGAGGAAAT[C/T]ATTAAAGGTTTTTGA | 11137 |
rs530515484 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107705907 | ATAATCCTTTGGGTA[C/T]ATACCCAGTAATGGG | 11137 |
rs530636051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107694053 | AAGTAGGCATGAAAA[C/T]AGGAATTTTTAAATT | 11137 |
rs530745189 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107700979 | AAGCAATCCCCCCGC[C/T]TCAGCTTCCCAAGTC | 11137 |
rs530790286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107705942 | CTGGGTCAAATGGTA[C/T]TTTTAGTTCTAGATC | 11137 |
rs530912013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107699829 | AAATACATATAACAT[A/G]AAAGTTAACACTTGT | 11137 |
rs530998961 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PWP1 | GRCh38.p7 | 12:107705555 | CCCCAGTGTGTGATG[A/T]TCCCCTTCCTGTGTC | 11137 |
rs531036500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107711905 | ATAAATCCAAGACAT[A/G]GCAAAGAAAGTAAAG | 11137 |
rs531046017 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107702390 | GGTTCAAGCTATTCT[C/T]GTGCCTCAGCCTCCT | 11137 |
rs531222016 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107685390 | AAGGTGAGAAAGTAA[C/T]ATTTAGGGATGTAAT | 11137 |
rs531262480 | in-del | -/GAAA | 0.00119737 | 0.0244387 | intron-variant | PWP1 | GRCh38.p7 | 12:107710829 | GTGTAGTCTTTTTAG[-/GAAA]GAAAGAGACAAGATC | 11137 |
rs531390491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107691447 | ATGGAACATACACTT[C/T]AGGAAGTTAACTCTG | 11137 |
rs531430891 | snp | A/G | | | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712624 | GCACAGGAGGCCATG[A/G]ACAGAGGCAAGTGCC | 11137 |
rs531470721 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PWP1 | GRCh38.p7 | 12:107704024 | TGTCACATGACAGAG[A/G]GCATGGATATAGGGA | 11137 |
rs531509668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107709936 | ATAAACCGTGGTTAC[C/T]TCCCTGAGAGATTTT | 11137 |
rs531512703 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107704482 | CACCAATTACTGAAA[C/G]TCAGCTCATTTTTTT | 11137 |
rs531558495 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107699984 | AATGAGGAGCAAAGT[C/T]ATGTCTTATATAGTG | 11137 |
rs531822308 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107684143 | TGAGAACAGACTACC[A/G]CAGTAGCCAAACTTT | 11137 |
rs531924570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107695894 | TCTATGAATGACCTA[A/G]AAGACAGGACCATTT | 11137 |
rs532281135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107691964 | GCCTTCATTCTTTTC[A/G]CTGCATCTTTTCTAT | 11137 |
rs532286086 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107711201 | TGCAGCAGGAACATG[A/C]CCTTAAGACACAGAT | 11137 |
rs532316838 | snp | C/T | 3.30006e-05 | 0.00406192 | synonymous-codon | PWP1 | GRCh38.p7 | 12:107704646 | TCTAGGTCAGTGGCT[C/T]TGTATGACTGCCGAA | 11137 |
rs532370768 | snp | C/G | 0.00014835 | 0.0086112 | synonymous-codon | PWP1 | GRCh38.p7 | 12:107710482 | AAAAGAAGGGCTTCG[C/G]GTCTGGGATATAAGC | 11137 |
rs532499633 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107685093 | ATCTTAGCTGAGAAG[C/T]ATGACATAGATACAA | 11137 |
rs532581741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107691314 | GGGCAGTTGCTGGGA[A/G]GTCTGGAAGAAAGAC | 11137 |
rs532583755 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107684235 | GGGGGTGTGGAAGTG[A/G]AGAAGTGGGTGTGGT | 11137 |
rs532619752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107690662 | GAGACAGGGTTTCAC[C/T]ATGTTGGCCGGGATG | 11137 |
rs532767744 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | PWP1 | GRCh38.p7 | 12:107696667 | TATGTATTCTCTTGA[A/C]TGTTTTCAGAATTGT | 11137 |
rs532851256 | snp | G/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107704379 | CATAGAGAGGATTCT[G/T]CTTGCGAGTGGAAGA | 11137 |
rs533021735 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PWP1 | GRCh38.p7 | 12:107709781 | CACAGCTGTTGAAAA[C/T]TGTGTATGAATAAAT | 11137 |
rs533060749 | snp | A/G | 3.29679e-05 | 0.00405991 | synonymous-codon | PWP1 | GRCh38.p7 | 12:107709208 | AGATAGGCCAAGTCT[A/G]GTTCATTCTAGGGAC | 11137 |
rs533224161 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PWP1 | GRCh38.p7 | 12:107695127 | AAAAATCAGCCAGGC[A/G]TGGTGGCGGGCGCCT | 11137 |
rs533286520 | in-del | -/CACA | 0.0130921 | 0.0798413 | intron-variant | PWP1 | GRCh38.p7 | 12:107696901 | TGATATGTGAGATGT[-/CACA]TACCAGCTAGAGTTC | 11137 |
rs533339007 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107701777 | CCACCTCTGGGGTTC[A/T]AGTGATTCTCCTGCC | 11137 |
rs533485700 | snp | C/T | 0.000247461 | 0.0111207 | missense | PWP1 | GRCh38.p7 | 12:107710505 | ATATAAGCACAGTCT[C/T]TTCAGGTAAGGATTT | 11137 |
rs533508802 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PWP1 | GRCh38.p7 | 12:107702367 | TTCTCTGCAACCTCC[A/G]CTTTTTGGGTTCAAG | 11137 |
rs533638795 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107701240 | TCAGGTGATCCTCCC[A/T]CCTCAGCCTCCCAAA | 11137 |
rs533659127 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PWP1 | GRCh38.p7 | 12:107689580 | GCGAAACCCTGTCTC[C/T]ACTAAAAATACAAAA | 11137 |
rs533678875 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107706869 | TTTGGCTTAGGATTG[A/T]CTTGGCAATGTGGGC | 11137 |
rs533745022 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107696096 | GGAGTGCAGTGGTGC[A/G]ATCTCAGCTCACTGC | 11137 |
rs533886831 | snp | C/T | | | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107683906 | AAAGTGCTGGGATTA[C/T]AGGCATGAGCCACTG | 11137 |
rs533970849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107703432 | CTTTTTCTTCTGAGT[A/G]TCTTCTAACATTTGA | 11137 |
rs534149735 | snp | C/G | | | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712937 | TAAGTATGAGTTTTA[C/G]TAGGCATTAAAAATC | 11137 |
rs534231560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107694491 | TCTTTAAGGCTGTCC[A/G]TGGGAAGCCTATAGA | 11137 |
rs534384791 | snp | C/G | 1.64933e-05 | 0.00287165 | utr-variant-5-prime, missense | PWP1 | GRCh38.p7 | 12:107688653 | AAGAGGAGACAGGCA[C/G]TCCTTCAGAAGATGG | 11137 |
rs534431059 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107706518 | TCTTCTAGGGTTTTT[A/C]TGGTTTTAGGTCTAA | 11137 |
rs534645424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107700866 | CCTAATGGGTATGAA[A/G]TGGTATATCATTGCG | 11137 |
rs534649009 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107687285 | TTTATAGAATAGGGA[C/G]AGAAAATTATTTCAT | 11137 |
rs534685670 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | PWP1 | GRCh38.p7 | 12:107686733 | GCACTTTGGGAGGCC[A/C]AGGCGGGCGGATCAC | 11137 |
rs534781992 | snp | G/T | 1.64893e-05 | 0.0028713 | stop-gained, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107693000 | TTTCCTCTCACTTAG[G/T]AACAATATGAACGTG | 11137 |
rs534819005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107699969 | TTATGGCAGAAAGCA[A/G]ATGAGGAGCAAAGTC | 11137 |
rs535126712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107692321 | TTTTTTCATATGCCA[A/G]TAAGGCATATTAGCA | 11137 |
rs535180199 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107701429 | GTGCTATCATTTGCA[G/T]CACAGGTTTTTCATG | 11137 |
rs535227391 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PWP1 | GRCh38.p7 | 12:107693410 | GAACTCCTGGGCTGA[C/T]GTAATCCTGATTTGG | 11137 |
rs535264985 | snp | A/G/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107690388 | AATAATAAAAAAGTT[A/G/T]AAAAAAGTTATAATC | 11137 |
rs535266736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107705345 | TTCCTGAAGTAAATA[C/T]GTAGTGCTTTGCAAA | 11137 |
rs535283213 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PWP1 | GRCh38.p7 | 12:107707126 | TTCACATTCCTTGTA[A/G]GTTGGATTCCTAGGT | 11137 |
rs535533104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107687374 | GAAGACTGATTTCCA[A/G]ATGAATCTACACATT | 11137 |
rs535628063 | snp | C/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107693692 | GCTGTGATTCTGTTT[C/G]CTCCACTGTACTCCA | 11137 |
rs535763261 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712875 | GTGAATAAGTCTTTG[C/T]TCTCCACCTAACAAG | 11137 |
rs536044140 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | PWP1 | GRCh38.p7 | 12:107686064 | ACCCGGAACTCGGGG[C/T]GTTGGCTGGTGCGAC | 11137 |
rs536125256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107700150 | TCCCACAACACATGG[A/G]AATTATGGGAGCTAC | 11137 |
rs536128756 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107692162 | TGCATATCAGATGTT[G/T]AAGACCTATCAGTCC | 11137 |
rs536161865 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107705698 | TCCCTACAAAGGACA[G/T]GAACTCATTCTTTTT | 11137 |
rs536225150 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107698647 | TGGAGTGCAGTGGCA[C/T]GATTATAGTTCACTG | 11137 |
rs536314126 | snp | A/C | 1.66358e-05 | 0.00288402 | intron-variant | PWP1 | GRCh38.p7 | 12:107704774 | AATGTTGTTGTTTTG[A/C]TTTTCTAGGTTGCTA | 11137 |
rs536566834 | snp | G/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107700608 | CTTCTGCCTTTTGGA[G/T]ACTGTGAATAATGCT | 11137 |
rs536597929 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107684289 | CTATTTATGACTTAA[C/T]CTTGGAAACATCATT | 11137 |
rs536630646 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107706288 | CATTGTAGATTCTGG[A/T]TATTAGCCCTTTGTC | 11137 |
rs536685832 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712681 | TGTTCTCAAATTAAT[A/G]CTCATGATTGAGTAT | 11137 |
rs536798298 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107701357 | TAACTCCTACTACCA[A/G]ATACATGATTTGCAA | 11137 |
rs536899372 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PWP1 | GRCh38.p7 | 12:107686662 | GGGTCCTGGGATAGG[C/T]ATGAACAAAATAGAA | 11137 |
rs537024121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107692237 | TTTTCCTGAGTTATC[C/T]TTTGTTACCATCGTA | 11137 |
rs537049558 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PWP1 | GRCh38.p7 | 12:107700288 | CCATCACCACAATGC[A/G]TCTCCAGAACATTTT | 11137 |
rs537077822 | snp | A/C | | | synonymous-codon | PWP1 | GRCh38.p7 | 12:107704679 | CCAGATGAAAGCCAT[A/C]GAATGTGGCGATTCA | 11137 |
rs537086552 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PWP1 | GRCh38.p7 | 12:107705722 | TCTTTTTTATGGCTG[C/T]ATAGTATTCCATGGT | 11137 |
rs537164844 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107703242 | GGTACAGAAAGGTAC[A/G]GTTACTAGGAACATT | 11137 |
rs537200054 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107698178 | ACCAGCCTGGCCAAC[A/G]TGGTGAAACCCTGTC | 11137 |
rs537394120 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, intron-variant | PWP1 | GRCh38.p7 | 12:107686113 | CTTTGCCCGGATTGT[C/T]GCGACTAGAGCTGCA | 11137 |
rs537409645 | snp | C/T | | | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107684076 | TGTGAGTCCATTAAA[C/T]CTCTTTTTCTTTATA | 11137 |
rs537639075 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107704860 | AACAGTATGAAGTAT[A/T]TGGGTTTAGGGTTGA | 11137 |
rs537677699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107710757 | TGTTTCTCAGCATTT[C/T]GGCTAAGACCAAGTG | 11137 |
rs537765565 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107710207 | GAACCAGCATGCTGC[A/G]CTTGTCTGGCTTCAT | 11137 |
rs537896926 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107684374 | TGGGGGCGGGGGGGG[C/G]TGCTTTGATGGAGGA | 11137 |
rs538018610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107697697 | TTTCAATCAGGTATT[C/T]TTGGTGAGATGGGGT | 11137 |
rs538102119 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | PWP1 | GRCh38.p7 | 12:107696904 | ATATGTGAGATGTTA[C/T]CAGCTAGAGTTCAGT | 11137 |
rs538144816 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PWP1 | GRCh38.p7 | 12:107703533 | CATGGTTTGCCCTTT[A/G]ATTATGCAGTACATT | 11137 |
rs538198996 | snp | G/T | 1.65026e-05 | 0.00287246 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107688683 | GCATGCAGAGTGCAC[G/T]CACCCAGGCACGCCC | 11137 |
rs538228969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107709342 | TTGCATTAACAAATA[C/T]GGATGTGTTGGGGAA | 11137 |
rs538529845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107698545 | AAAAAATAAACTACT[A/G]TAGTTTCTTCCCTGT | 11137 |
rs538693026 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PWP1 | GRCh38.p7 | 12:107703597 | CGCATTTATAGAAAT[A/T]CTGTCAAATAGATTC | 11137 |
rs538819275 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107684484 | ATGGTCTTTCTAAAA[C/T]GGGTTAAAAGCAAAG | 11137 |
rs538821524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107691546 | GGCCAGAAGCAATGA[A/G]GGCCTGGCTTGGGGC | 11137 |
rs538909690 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107690916 | GGGTATCTGGAAGAG[C/G]AGTGTAGTTGGAGTG | 11137 |
rs538942639 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107705006 | GATTTTGATCATTTT[A/G]TTGTAGTGTTGTTTG | 11137 |
rs538986894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107689989 | CTTGGGGTTTGAGAA[A/G]TAGGCATTTGGCACA | 11137 |
rs539005409 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107710181 | CAGAAGTTGCAGATA[C/T]CATTGTGGAAGAACC | 11137 |
rs539020361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107704074 | ACTGTGGTCAACCAC[A/G]GGGTTTATAGCTCAT | 11137 |
rs539119797 | snp | C/T | 1.65157e-05 | 0.0028736 | synonymous-codon, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107688708 | ACGCCCAAGAGAGCC[C/T]CTGGAGGATGGTGAC | 11137 |
rs539169274 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107695232 | GATCGTGTCACTGCA[C/T]TCCAGCCTGGGCGAC | 11137 |
rs539486444 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107686944 | GCACTCCAGCCTGGG[C/T]GGGCAACAGAGTGAG | 11137 |
rs539643588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107708635 | AGTAGCCATGCTCAC[C/T]AGGCCTGTGTTCACG | 11137 |
rs539740433 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107708034 | AATTCTGCACGATTA[A/G]TAGAGGTGCATGCTG | 11137 |
rs539743277 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107707413 | TGCCTGATTGCCCTG[C/G]CCAGAACTTCCAACA | 11137 |
rs539821132 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107689623 | TGGTGGCGCACATCT[A/G]TAATCCCAGCTACTC | 11137 |
rs539850981 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107695031 | GAGGCCAAGGCGGGC[A/G]GATCACGAGTTCAGG | 11137 |
rs539897230 | snp | A/C | | | intron-variant | PWP1 | GRCh38.p7 | 12:107712005 | TTGGTTACTCACTTT[A/C]CCATTTATAAAGTAC | 11137 |
rs540016131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107687449 | GTCCCACTCCCAAGT[A/G]TTGTGTTGTAATTAG | 11137 |
rs540120323 | snp | A/T | 0.00145042 | 0.0268906 | intron-variant | PWP1 | GRCh38.p7 | 12:107688565 | ACCATGTGGTCTTGT[A/T]ATTAGAAGGTAGCAT | 11137 |
rs540122716 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107688282 | TTATTTGTAAGAATC[C/T]ATAAAATCTATATTT | 11137 |
rs540161513 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107694941 | TATTGATCTCACGTG[A/G]TTAAGAGTATATTTT | 11137 |
rs540349817 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107708184 | CTAACAAATGGTCAT[A/G]TATATTAGAATCCCA | 11137 |
rs540388508 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | PWP1 | GRCh38.p7 | 12:107705524 | ATCCCTCCCCCTCCC[A/C]CCACCCCACGACAGG | 11137 |
rs540454853 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107695366 | TAATAATTTTGAACA[G/T]GAATTCTCATCACAG | 11137 |
rs540553942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107702206 | AGTACTATTTTGGCT[A/G]TTCTAGGTTCCTTGC | 11137 |
rs540704027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107693246 | AGGTGGCCAATTTCT[C/T]GGTTATTGTTCTGGG | 11137 |
rs540748606 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107706716 | GATGATTGTAGATGT[A/G]TGGTATTATTTCTGA | 11137 |
rs540788646 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107700430 | CATATGAATGGAATC[A/C]TACAGACTTACTTCT | 11137 |
rs540870787 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712358 | TCCTTTCTGCAACTG[C/T]GGTGGCACCACAAAT | 11137 |
rs541015308 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107693937 | TAATAATTCAACACA[A/T]AGGGCCACGTTTCTT | 11137 |
rs541022937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107687017 | AGAAAAAGACCCTGC[C/T]TTTATGGAGTCGACA | 11137 |
rs541097730 | in-del | -/A | | | intron-variant | PWP1 | GRCh38.p7 | 12:107694683 | AATTGAGAACCTATT[-/A]AGAGTTTTTTTTGTC | 11137 |
rs541101881 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107686153 | GTCTGGTTCGCCTGA[A/G]CCTGGAGAGTCAAGG | 11137 |
rs541138882 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107685779 | CCAAACAGGAGCCTG[C/T]GCATGCGCTCTGCCC | 11137 |
rs541178451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107699613 | GCATCCTCCAGGTCA[C/T]CTGCCAGCTCATCAC | 11137 |
rs541295141 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107698820 | CTGGTCTCGAACTCC[C/T]GGCCTCAAGCGATGT | 11137 |
rs541467648 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107694168 | TATGCTAAAAGTAGA[C/T]TTGCACAATGTCTGG | 11137 |
rs541612700 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107693337 | AAATTTTTCATAGGG[A/G]TGTTTTTTTTTGTTT | 11137 |
rs541613150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107700897 | GTTTTAATTTGCATT[C/T]CCCCCCCTTTTTTTA | 11137 |
rs541768187 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107704896 | TAAGGTGTTTTTTTT[A/T]AAATAAGAGAACGGC | 11137 |
rs541772913 | snp | C/T | 0.175254 | 0.238565 | intron-variant | PWP1 | GRCh38.p7 | 12:107705864 | ATATGCACATACGTG[C/T]GCATGTGTCTTTATA | 11137 |
rs542011338 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107701749 | GTGGTGTGATCTCAG[C/T]TCACTGCACCCCCCA | 11137 |
rs542126494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107692465 | CATTTTATTTCCAGG[C/T]CCTCAAGGCTGCCTC | 11137 |
rs542472112 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107685811 | GGCAGCGGCCCTGTG[C/T]AGATCCCTGAGCGTG | 11137 |
rs542516663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107691805 | TCCGTTTTCCTCATT[C/T]GCTTGGCCATCTGTC | 11137 |
rs542549803 | in-del | -/TC | | | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107684602 | TTACTTCTGGGAGGA[-/TC]TCTCCTCAGGCAGGG | 11137 |
rs542595651 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107684852 | TTTGACAATGCCACT[A/G]GGAAAGACCATGTGT | 11137 |
rs542634512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107690999 | AAACAACAGACAGGC[A/G]ATGAGAAATGAGTAA | 11137 |
rs542715315 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107697218 | GATTGAGCCTTTCCT[A/C]CTCAAATTGTGGCCC | 11137 |
rs542846884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107696417 | TTTTTTTGAGCGGGA[C/T]GTGATTTTTGATGAC | 11137 |
rs542881971 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107709546 | ACCCTGAAATCAAGA[C/G]CATCCCAAGAAATCT | 11137 |
rs542921282 | snp | A/C | | | intron-variant | PWP1 | GRCh38.p7 | 12:107701461 | GATGGTGTCTACTTT[A/C]TTTCTTTTGTTGTTC | 11137 |
rs543084092 | snp | G/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107691004 | ACAGACAGGCAATGA[G/T]AAATGAGTAAGTAGG | 11137 |
rs543164338 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107711623 | TATTTATTACTTTGA[C/G]GTAGTCTGGTGCGTT | 11137 |
rs543261132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107711156 | AACGAGGGATAGGCC[A/G]GATTAAAGGAATGGG | 11137 |
rs543599642 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PWP1 | GRCh38.p7 | 12:107698086 | TGCTAGGCCAGGCCA[C/T]GCACGTGGCTCACTC | 11137 |
rs543599784 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107690635 | GCCCAGCTAATTTTC[A/G]TGTTTTTAGTAGAGA | 11137 |
rs543681833 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PWP1 | GRCh38.p7 | 12:107704277 | TGATAAACTGCTTAT[A/G]GAGAGTAAGTGTGCC | 11137 |
rs543920809 | snp | C/T | 0.000164891 | 0.00907846 | synonymous-codon | PWP1 | GRCh38.p7 | 12:107709145 | AATCAAGGGCTGTCT[C/T]GTGACTGCTTCAGCT | 11137 |
rs544181563 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107689128 | ATCCATATACCTTTT[C/T]CTCAACTGCAGTCAG | 11137 |
rs544280932 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107704063 | GAACTGGGGCCACTG[C/T]GGTCAACCACGGGGT | 11137 |
rs544429246 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107707673 | TGGTTTTTGTCTTTG[C/G]TTCTGTTTATATGCT | 11137 |
rs544483046 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PWP1 | GRCh38.p7 | 12:107689603 | ATACAAAACTTAGCC[A/G]GGCGTGGTGGCGCAC | 11137 |
rs544607882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107695504 | TTCTTAATACAAAGC[A/G]TATGGGGAGGGGTTC | 11137 |
rs544642652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107702319 | AGAGTCTCACTCTGT[C/T]GCTCAGGCTGGAGTC | 11137 |
rs544723196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107703832 | TGGTACCCAGGCAGA[A/G]TGTATCCTTGAGGCC | 11137 |
rs544732436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107701739 | GCTAGAGTGAGTGGT[A/G]TGATCTCAGCTCACT | 11137 |
rs544980264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107704306 | CCTAAGACATGAGTA[A/G]CCTGGCTCTGAGCTC | 11137 |
rs544998811 | in-del | -/T | 0.00478085 | 0.0486577 | intron-variant | PWP1 | GRCh38.p7 | 12:107698575 | TTCCTTGTAATGAAA[-/T]TTTTTTCTTTATTTT | 11137 |
rs545031620 | in-del | -/AT | | | intron-variant | PWP1 | GRCh38.p7 | 12:107703620 | ATAGATTCTTACCAC[-/AT]GTTAGGTAATTTTAC | 11137 |
rs545069698 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107710239 | TTGTAGTACTAGCCC[G/T]TCTGACTTGACTCTG | 11137 |
rs545192284 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107695634 | TGTGAATATTAAGGA[G/T]CTGTTGCCATATTCC | 11137 |
rs545419097 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PWP1 | GRCh38.p7 | 12:107689720 | CACTGCACTCCAGCC[C/T]GGGTGACACAGTGGG | 11137 |
rs545504680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107688259 | GAAGTTTCAGGTAGC[A/G]AGAGATCTTATTTGT | 11137 |
rs545520779 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107687750 | AAAAATTAAAATTAA[A/G]GCCGGGCACGGTGGC | 11137 |
rs545631233 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107694070 | GGAATTTTTAAATTG[C/T]ATTTTTAAATGTTGT | 11137 |
rs545736705 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107690704 | CTGACCTCATGATCC[A/G]CCTGCCTCGGCCTGA | 11137 |
rs546061405 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PWP1 | GRCh38.p7 | 12:107698925 | ATGAGTCTCTAACAG[A/G]GAGACAAGGTTTTAT | 11137 |
rs546142043 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107708523 | GCCACACTGGTCGAT[C/T]TGACTGTTGGTCACG | 11137 |
rs546226306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107705971 | TCCTTGAGGAATTGC[C/T]ATACTGTCTTCCACA | 11137 |
rs546229006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107708029 | ATCTCAATTCTGCAC[A/G]ATTAGTAGAGGTGCA | 11137 |
rs546296934 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712542 | TAGAATTTTTAAAGC[G/T]TAAAATCCGGTAATA | 11137 |
rs546456734 | snp | G/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107709307 | TGGAACTTGTGTTGC[G/T]TGTTTTTCTGTTGGA | 11137 |
rs546461226 | snp | A/C | | | intron-variant | PWP1 | GRCh38.p7 | 12:107705652 | GCGATAGATAGTTTT[A/C]TGAGAATGATGGTTT | 11137 |
rs546492747 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PWP1 | GRCh38.p7 | 12:107686834 | AGCCGGGTGTGGTGG[C/T]GGATGCCTGTAGTCC | 11137 |
rs546529747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107686306 | TTTTTGACAACACCA[C/T]TAGCTTCACTAGCAC | 11137 |
rs546529797 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107693183 | CATTTTTAGGTGCCA[C/G]ATCCTATTGTATCTC | 11137 |
rs546708206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107693572 | GAAGTAAAATTATAT[A/G]TAAAAATACAAGGCT | 11137 |
rs547047006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107701123 | GAGAAATGTTTTTCA[A/G]GTCCTTTGCTTACTT | 11137 |
rs547125632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107699995 | AAGTCATGTCTTATA[C/T]AGTGGCAGGCAGGAG | 11137 |
rs547132122 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107700592 | GTCACCTGGATTGCT[G/T]CTTCTGCCTTTTGGA | 11137 |
rs547256714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107705639 | GTTTTCTGTCCTTGC[A/G]ATAGATAGTTTTCTG | 11137 |
rs547304607 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107699020 | TGTAATCCCAACACT[C/T]TGGGAGGCCGAGAGT | 11137 |
rs547342505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107711203 | CAGCAGGAACATGCC[C/T]TTAAGACACAGATCG | 11137 |
rs547449708 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107686490 | TCTTGCAGTAATCCA[A/T]GTGAGATGTTGATGG | 11137 |
rs547489646 | snp | G/T | 3.44092e-05 | 0.0041477 | intron-variant | PWP1 | GRCh38.p7 | 12:107692775 | TGTTTTTGTCAAGAT[G/T]ACTATTTTATTATTG | 11137 |
rs547519454 | snp | C/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107704444 | TAGAGGCACCAGTGC[C/G]TTCAAGTGTTAAGAT | 11137 |
rs547620322 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107684237 | GGGTGTGGAAGTGGA[G/T]AAGTGGGTGTGGTGG | 11137 |
rs547626721 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | PWP1 | GRCh38.p7 | 12:107701588 | ACATTGAAGTCTATG[-/A]TCCATTTTGAGTTTT | 11137 |
rs547686199 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PWP1 | GRCh38.p7 | 12:107698592 | TTTTTCTTTATTTTT[C/T]TTTTTTAAAGAGGTA | 11137 |
rs547705460 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107690664 | GACAGGGTTTCACCA[C/T]GTTGGCCGGGATGGT | 11137 |
rs547726373 | snp | C/T | | | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107684665 | TGGTGACAGAACTCA[C/T]AGTTGTATCAGCTCC | 11137 |
rs547840794 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712670 | TCATTCCTAACTGTT[A/C]TCAAATTAATGCTCA | 11137 |
rs548007613 | snp | C/T | 4.95242e-05 | 0.0049759 | synonymous-codon, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107692830 | TGCTGAGACTCTTGG[C/T]GAATCTCTCTTGGGT | 11137 |
rs548028042 | snp | A/C/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107686521 | TAGCAGGGAGGATGA[A/C/G]AGGTAAATGTCTAAC | 11137 |
rs548050485 | snp | C/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107687085 | CCAAACAGTAAAAGG[C/G]GTTGATTTGAATGTA | 11137 |
rs548069972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107686519 | GGTAGCAGGGAGGAT[A/G]AGAGGTAAATGTCTA | 11137 |
rs548091511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107699785 | TCTCACCACATACTC[C/T]TTTATTCTTTTTTCT | 11137 |
rs548330691 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107705252 | GCATCCAAAGATTCC[A/G]CTGACATTTCAGTAC | 11137 |
rs548380081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107711223 | GACACAGATCGAGAT[C/T]GCTCATGCTATTGTT | 11137 |
rs548601717 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107685331 | AGTATATAATTGGTG[C/T]TAAATGTTTTTTTCT | 11137 |
rs548690647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107691406 | GAGGAAATCATTAAA[A/G]GTTTTTGAGCATGGA | 11137 |
rs548725731 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PWP1 | GRCh38.p7 | 12:107710640 | CAATCCTTGGTCCTC[A/G]GCCTTCTGTATAGCT | 11137 |
rs548733657 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107692352 | TATCAGAACACGTGC[A/G]GTAGAGCAACCTGGT | 11137 |
rs548987881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107690703 | CCTGACCTCATGATC[C/T]GCCTGCCTCGGCCTG | 11137 |
rs549025602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107698342 | AGCCTGTGTGACAGA[A/G]CGAGACTCTGTCTCA | 11137 |
rs549239900 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107703440 | TCTGAGTATCTTCTA[A/T]CATTTGAGGGACTAA | 11137 |
rs549283461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107702426 | ACTGGGATTACAGGC[A/G]TGCGCCACCATGCCC | 11137 |
rs549429254 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PWP1 | GRCh38.p7 | 12:107695101 | TCTACTAAAAATACA[A/C]AAAAAAAAAAAAAAA | 11137 |
rs549542883 | in-del | -/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107705372 | AAAGGTGAGAAAGAG[-/T]TTTTTTTTTTTTTTT | 11137 |
rs549548199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107689215 | GTTAGCCACAGTCAA[C/T]TGCAGTCTGAAAATA | 11137 |
rs549650770 | snp | G/T | 1.6489e-05 | 0.00287128 | missense | PWP1 | GRCh38.p7 | 12:107710428 | CTTCTGTTCTTCATG[G/T]TGCCCTGATTTGCCA | 11137 |
rs549756436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107704511 | TTTCTACTTTATTTA[A/G]AACCTTAAAACAGGC | 11137 |
rs549837168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107691876 | ACTTAGAAAGGAATC[A/G]TTACCTCCATTTACC | 11137 |
rs549913611 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107689678 | TTGAACCTGGGAGGC[A/G]GAGGTTGCAGTGAGC | 11137 |
rs549963855 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107698499 | TGCCACTGCACTCCA[A/C]CCTGGGTGACAGAGC | 11137 |
rs550009880 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107684196 | ACATTAGTGTTCTAC[C/T]GGTGGGCAGTGGGGG | 11137 |
rs550049108 | snp | A/G | 0.000126622 | 0.00795582 | intron-variant | PWP1 | GRCh38.p7 | 12:107697734 | TTATGAAATTATTGT[A/G]ATTTTTAGTTTTGAA | 11137 |
rs550084338 | snp | G/T | 1.64868e-05 | 0.00287109 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107696578 | CCTAGCCCAGATGAT[G/T]CTACTGGTAATTAGA | 11137 |
rs550084450 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PWP1 | GRCh38.p7 | 12:107689554 | AGTTCGAGACCAGCC[A/G]GGCCAACATGGCGAA | 11137 |
rs550086278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107711327 | CCACAACCTTCCAGC[C/T]TGGGCGTTAGGGCCA | 11137 |
rs550120912 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107695895 | CTATGAATGACCTAG[A/T]AGACAGGACCATTTA | 11137 |
rs550267961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107703142 | ATTTTATCTGGCTTG[C/T]GGCATGCTTTCACAT | 11137 |
rs550475801 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107708088 | TGACTTATTTTTACA[A/G]TGATCATTCCAGTTG | 11137 |
rs550596903 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107705987 | ATACTGTCTTCCACA[A/G]TGGTTGAACTAGTTT | 11137 |
rs550730699 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107702623 | GAAAGAAAAAAGTCA[C/T]CAGAGATTTTGAAAG | 11137 |
rs550920942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107690001 | GAAATAGGCATTTGG[C/T]ACACTGAGCAGGTTA | 11137 |
rs551146229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107701222 | GTCTTGACCTTCTGG[A/G]GCTCAGGTGATCCTC | 11137 |
rs551194532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107706798 | TGCTGTTTTGGTTAC[C/T]GTAGCCTTGTAGTAT | 11137 |
rs551244839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107700618 | TTGGATACTGTGAAT[A/G]ATGCTGCTATGAATG | 11137 |
rs551572590 | snp | C/T | 9.92244e-05 | 0.00704289 | intron-variant | PWP1 | GRCh38.p7 | 12:107709250 | AAGAATCTCCCTGGG[C/T]ATCTGTTTTTTATTT | 11137 |
rs551734317 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107694344 | TTAGGCTGATAAGTC[C/G]TTTTGTTATAGGAAA | 11137 |
rs551849641 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712700 | ATGATTGAGTATTCT[C/T]AGTGCAACTCGTAGA | 11137 |
rs551907961 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107695051 | ACGAGTTCAGGAGAT[C/G]GAGACCATCCTGGCT | 11137 |
rs551924177 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107696276 | GACCTCAAGTGATCC[A/G]CCCACCTTGGCCTCC | 11137 |
rs552091659 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PWP1 | GRCh38.p7 | 12:107710144 | AGACAGAGTGATAAC[A/G]AAGATGAGTGGCCTG | 11137 |
rs552110406 | snp | A/G | 1.65351e-05 | 0.00287528 | intron-variant, splice-acceptor-variant | PWP1 | GRCh38.p7 | 12:107692970 | TGGCTCTCTGCTTCT[A/G]GTCAATGACATTTTT | 11137 |
rs552373727 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PWP1 | GRCh38.p7 | 12:107705585 | CCAAGTGTTCTCATT[C/G]TTCAATTCCCACCTA | 11137 |
rs552628472 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107707014 | TATTTTCACAATATT[C/G]ATTCTTCCTATCCAT | 11137 |
rs552709572 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107705283 | ATGTAAAAAGAAAAG[A/C]CCAGCTTTCATCCAG | 11137 |
rs552731398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107693960 | CGTTTCTTTTTTGGA[A/G]CCAAAACATCGTGAT | 11137 |
rs552749590 | snp | C/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107701590 | ATTGAAGTCTATGAT[C/G]CATTTTGAGTTTTTT | 11137 |
rs552926507 | snp | A/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107698849 | GTTCCCACGTTAGCT[A/T]CCCAAGGTCCTGGGA | 11137 |
rs553143237 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712821 | AAACACTGAATGCCA[C/T]TCTGTGCCTAGTGCT | 11137 |
rs553230777 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | PWP1 | GRCh38.p7 | 12:107705334 | TTGCCCAGTTTTCCT[-/G]GAAGTAAATATGTAG | 11137 |
rs553246580 | snp | A/G | 0 | 0 | intron-variant | PWP1 | GRCh38.p7 | 12:107692405 | TCTCAATTTTATTTG[A/G]CCAGGCAACCCTTAT | 11137 |
rs553302124 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107703590 | AGAGGGACGCATTTA[C/T]AGAAATACTGTCAAA | 11137 |
rs553332394 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PWP1 | GRCh38.p7 | 12:107699254 | ACAGACAAAGACTCC[A/G]TCTCAAAACAAAACA | 11137 |
rs553451618 | snp | C/G | 1.64806e-05 | 0.00287054 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107693058 | ATCTTATAGTTTGTG[C/G]CCGAGCTGAACAGGA | 11137 |
rs553603725 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107689101 | ATAATGCTATGGTGT[A/G]CTTGAACTTATATCC | 11137 |
rs553727239 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107697079 | GTTTATACTGTCTTA[C/G/T]GTCTTGTTTGCACAC | 11137 |
rs553759440 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107684091 | CCTCTTTTTCTTTAT[A/G]AATTATCATGTCTTG | 11137 |
rs553766746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107704935 | AAAAAGCAGTGAACA[C/T]GTAAATGATTTTGCT | 11137 |
rs553792295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107704112 | CTCCTTTTTACAGAT[C/T]GGGTCTACAGGTAGG | 11137 |
rs553797895 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107690929 | AGCAGTGTAGTTGGA[A/G]TGTGGAAAGAATAGG | 11137 |
rs553805458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107710984 | TTAAAGACACACACA[C/T]AGAAATATAGAGATG | 11137 |
rs553834477 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PWP1 | GRCh38.p7 | 12:107697829 | TACACAAAACTAGTT[C/T]AAAGCTAGTATATTA | 11137 |
rs553914383 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107709476 | CTTGGTAAGGCTGGG[G/T]AGAGGGTTTTCTAGG | 11137 |
rs553949313 | snp | C/G | 0.000396616 | 0.0140766 | intron-variant | PWP1 | GRCh38.p7 | 12:107709040 | GAGTAATGCTTCTTT[C/G]ATTTTTCTTAACTTA | 11137 |
rs554002963 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107708349 | TTTCTTGTACTGGCT[A/G]TTGCCCTTGGCCTGT | 11137 |
rs554235794 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107710699 | GCCTCTCCTCTTTCT[A/G]AATGAGTTCTGTAAG | 11137 |
rs554261822 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | PWP1 | GRCh38.p7 | 12:107694257 | TCCTCAGACAAGTCC[A/G]TCCTTGCCCGATACT | 11137 |
rs554357319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107711567 | AAAATCCAACTTTCC[A/G]GAAGGGGCCACTCCT | 11137 |
rs554523772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107705706 | AAGGACATGAACTCA[C/T]TCTTTTTTATGGCTG | 11137 |
rs554582710 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107698667 | ATAGTTCACTGCAGC[C/G]TGAAACGCCTAGGCT | 11137 |
rs554584091 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107685637 | TGAAAAGCCTTTTCT[C/G]TATACTTCACACAGC | 11137 |
rs554642039 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107705377 | GTGAGAAAGAGTTTT[G/T]TTTTTTTTTTAAATT | 11137 |
rs554717433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107704232 | GATTCACGCAGAATT[A/G]CAAAAGTGCATCCCT | 11137 |
rs554777543 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | PWP1 | GRCh38.p7 | 12:107686070 | AACTCGGGGCGTTGG[C/T]TGGTGCGACTGGCTG | 11137 |
rs554911245 | snp | C/G/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107700664 | TCAAGTCCCTGCTTT[C/G/T]AGTTGTTTTGAGTAT | 11137 |
rs554954662 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107697990 | CATGTATTAACTCCT[A/G]CAGCTTTTAAAATCG | 11137 |
rs554995238 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PWP1 | GRCh38.p7 | 12:107691086 | TGCCTCAGGCAGGGC[A/G]TGTTTGAGCACAGTA | 11137 |
rs555043960 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107694292 | TCCCCCAGCAGTCTT[C/T]AGATCGTCTTGAAAC | 11137 |
rs555098732 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107683883 | TAATCCAACTGCCTC[A/G]GCCTCCCAAAGTGCT | 11137 |
rs555491139 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107689596 | ACTAAAAATACAAAA[A/C]TTAGCCAGGCGTGGT | 11137 |
rs555551009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107696892 | ATAAATGGCCTGATA[C/T]GTGAGATGTTACCAG | 11137 |
rs555675644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107702813 | AAGTCTTACATTTCT[C/T]TTGTTAAATTTATTC | 11137 |
rs555732818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107708147 | CTCACTCTTCAGGTA[C/T]GCAACTTCCAGAGAT | 11137 |
rs555848117 | snp | G/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107708179 | ATTTGCTAACAAATG[G/T]TCATATATATTAGAA | 11137 |
rs556002387 | snp | G/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107687089 | ACAGTAAAAGGGGTT[G/T]ATTTGAATGTACTTG | 11137 |
rs556004646 | snp | G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107684406 | TATCAAGATCACGTT[G/T]CAGACAAACATGTGT | 11137 |
rs556038027 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | PWP1 | GRCh38.p7 | 12:107688017 | GCCTGGGCAACAGAG[C/G]GAGACTCCGTCTCAA | 11137 |
rs556280331 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PWP1 | GRCh38.p7 | 12:107684022 | TTCTTCTCTTTTGCC[G/T]TCTGCAGTGATTGTG | 11137 |
rs556292845 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107709372 | AGTGAATTTTGAGTT[G/T]AGTCAAATTTGGTGG | 11137 |
rs556440812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107690239 | AGACATAGCAGAGCT[A/G]AGCGTGGTGGCTCAT | 11137 |
rs556494213 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107711445 | TAAAATTGAAAGATC[C/T]TTGGGGAAAGCTGGA | 11137 |
rs556499588 | snp | C/G | 0.000399281 | 0.0141238 | missense, utr-variant-5-prime | PWP1 | GRCh38.p7 | 12:107688691 | AGTGCACGCACCCAG[C/G]CACGCCCAAGAGAGC | 11137 |
rs556516674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107690637 | CCAGCTAATTTTCGT[A/G]TTTTTAGTAGAGACA | 11137 |
rs556567319 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107696266 | TCGAACTCCTGACCT[C/G]AAGTGATCCGCCCAC | 11137 |
rs556624923 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107694778 | AAAGAGGAGCTGAGA[A/C]AGAAGTTAAAGCTGT | 11137 |
rs556765584 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107702154 | AGTAAGTTTTGATGC[C/G]AGGAAATATGAACTT | 11137 |
rs556972053 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PWP1 | GRCh38.p7 | 12:107706634 | GCTAGCCAGTTTTCC[C/T]AGCACCATTTATTAA | 11137 |
rs557002782 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PWP1 | GRCh38.p7 | 12:107712882 | AGTCTTTGCTCTCCA[C/T]CTAACAAGGGACAGT | 11137 |
rs557129302 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107707200 | GATTTGGCTGTTTGT[C/G]TATTATTGGTGTATA | 11137 |
rs557202006 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107701372 | AATACATGATTTGCA[A/G]ATATTTTCTTCTATT | 11137 |
rs557233329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107686773 | AGATCGAGAGCATCC[C/T]GGCTAACACGGTGAA | 11137 |
rs557362525 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PWP1 | GRCh38.p7 | 12:107697290 | AGTTAGAAATGCCCA[C/G]CCAGAACCACCTGAA | 11137 |
rs557377413 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PWP1 | GRCh38.p7 | 12:107689574 | AACATGGCGAAACCC[C/T]GTCTCTACTAAAAAT | 11137 |
rs557584405 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PWP1 | GRCh38.p7 | 12:107695978 | GGGGTATGCCACAAG[A/G]TGGCACTGTATTAGA | 11137 |
rs557658133 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107702430 | GGATTACAGGCATGC[A/G]CCACCATGCCCAGCT | 11137 |
rs557674986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107700199 | GGTGGGGACATAGCC[A/G]AATCCTATCACCATT | 11137 |
rs557750086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107701545 | TTTACATGTATGTTT[C/T]CTTCTGAGTTTTATA | 11137 |
rs557982576 | snp | C/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107708055 | GTGCATGCTGTTCTA[C/G]CCAGGCAGCCTGAAG | 11137 |
rs558071340 | snp | C/T | | | intron-variant | PWP1 | GRCh38.p7 | 12:107693593 | ATACAAGGCTGGGTG[C/T]GGTGTCTCACACCTG | 11137 |
rs558136135 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PWP1 | GRCh38.p7 | 12:107706324 | AGTAGATTGCAAAAA[A/T]TTTCTCCTATTCTGT | 11137 |
rs558363583 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PWP1 | GRCh38.p7 | 12:107705742 | TATTCCATGGTGTAT[A/C]TGTGCCACATTTTCT | 11137 |
rs558417640 | snp | A/G | | | intron-variant | PWP1 | GRCh38.p7 | 12:107690464 | TGAGTAAAATAATAT[A/G]CTTTTTTTTGTGTGT | 11137 |