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 |