SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs700481 | snp | A/G | 0.460589 | 0.13473 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3809309 | ACATCCATTAACTCT[A/G]TACTATCATATTTTA | 57097 |
rs719352 | snp | C/T | 0.499816 | 0.0095829 | intron-variant | PARP11 | GRCh38.p7 | 12:3833417 | gcaagcctggcaaca[C/T]agtgagactccatct | 57097 |
rs727703 | snp | C/G | 0.489665 | 0.0711382 | intron-variant | PARP11 | GRCh38.p7 | 12:3837753 | gtggaacatctttat[C/G]ccttcactttcatcc | 57097 |
rs727704 | snp | C/G | 0.410737 | 0.191478 | intron-variant | PARP11 | GRCh38.p7 | 12:3837662 | TTTTTTTTTTTCTTC[C/G]CCATTCAGCCACTCT | 57097 |
rs727705 | snp | G/T | 0.172997 | 0.237846 | intron-variant | PARP11 | GRCh38.p7 | 12:3837468 | TTTTAACTCATTAGT[G/T]TTTATTTTTAGTGGG | 57097 |
rs758799 | snp | G/T | 0.240765 | 0.249829 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3809134 | TTATTCTAGGTTTAT[G/T]TCTATTCATTCTCCC | 57097 |
rs1860617 | snp | A/C | 0.470908 | 0.117046 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3809706 | AAATTACAAATAAAT[A/C]GAAAAAAAGATTTTC | 57097 |
rs1986922 | snp | C/G | 0 | 0 | intron-variant | PARP11 | GRCh38.p7 | 12:3814225 | ACACAAAAGCACACA[C/G]AAATATACCATAAGT | 57097 |
rs2072386 | snp | G/T | 0.488485 | 0.0749998 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3841016 | CTGCTCCAATTCCTG[G/T]TCGGTCAGTGACACA | 57097 |
rs2072387 | snp | C/T | 0.488726 | 0.0742286 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3841018 | GCTCCAATTCCTGGT[C/T]GGTCAGTGACACAGA | 57097 |
rs2072388 | snp | C/G | 0.126909 | 0.217598 | intron-variant | PARP11 | GRCh38.p7 | 12:3841083 | AACTCATTTAACACC[C/G]TCTCCAGTTCCTGTG | 57097 |
rs2159606 | snp | C/G | 0.125874 | 0.217008 | intron-variant | PARP11 | GRCh38.p7 | 12:3819046 | CTACACCACTCTTCT[C/G]AACTCCTGACCCATA | 57097 |
rs2231377 | snp | C/T | 0.241053 | 0.24984 | intron-variant | PARP11 | GRCh38.p7 | 12:3830602 | GGTGGTAGATTGTTA[C/T]ATATACATCCAGACT | 57097 |
rs2231378 | snp | C/T | 0 | 0 | intron-variant | PARP11 | GRCh38.p7 | 12:3830321 | TAAAATTGAAAATGC[C/T]TGGGGCTATGCTGAA | 57097 |
rs2231379 | snp | A/T | 0.0475351 | 0.146656 | intron-variant | PARP11 | GRCh38.p7 | 12:3828759 | TATAAAAATTCAAGT[A/T]TTAAAATCTTGAGCA | 57097 |
rs2231380 | snp | C/G | 0.120674 | 0.21395 | intron-variant | PARP11 | GRCh38.p7 | 12:3814332 | GAAATTATTTCTTTT[C/G]TAGACTTGCTTTGTC | 57097 |
rs2231381 | snp | C/T | 0.150667 | 0.229419 | intron-variant | PARP11 | GRCh38.p7 | 12:3813895 | TAATTGCATTGTGTA[C/T]GAGAATAGATACTAG | 57097 |
rs2878785 | snp | C/G | 0.433963 | 0.169285 | intron-variant | PARP11 | GRCh38.p7 | 12:3823195 | GAAAAAAATCAAATA[C/G]GTGATTTAAAAATTA | 57097 |
rs3079895 | in-del | -/AA | 0.24019 | 0.249807 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3809355 | AGTTCTCTCTTATAA[-/AA]GAGGGGTTGGCAGTA | 57097 |
rs3082900 | in-del | -/TA | | | intron-variant | PARP11 | GRCh38.p7 | 12:3814796 | AGAGAAATGAATATA[-/TA]GTCATGTATTTACAT | 57097 |
rs3168623 | snp | C/T | 0.120326 | 0.21374 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3808872 | GATGATTAAAGCTCT[C/T]CATTAGCAGTTCTTG | 57097 |
rs3214323 | in-del | -/T | 0.12932 | 0.218944 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812001 | TTATATGGAGGCCAC[-/T]TTTTTTCATATCTGT | 57097 |
rs3741933 | snp | C/T | 0.120674 | 0.21395 | intron-variant | PARP11 | GRCh38.p7 | 12:3814406 | CATAATTTTCAACCT[C/T]AAGTTTCAGTGTTAA | 57097 |
rs3759357 | snp | G/T | 0.12932 | 0.218944 | intron-variant | PARP11 | GRCh38.p7 | 12:3832626 | CATAATTATGCAAAA[G/T]AGTCATTTCTTTGGA | 57097 |
rs3759358 | snp | A/T | 0.416708 | 0.186302 | intron-variant | PARP11 | GRCh38.p7 | 12:3831467 | CCTAGACAAGGCAAT[A/T]GAAACTTATTCCAGG | 57097 |
rs3759359 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3831329 | ATACAGGAAATCAAA[G/T]TTTTAACAAATCATC | 57097 |
rs3759360 | snp | C/T | 0.494442 | 0.0524218 | intron-variant | PARP11 | GRCh38.p7 | 12:3830806 | GAATCTTGACTTCCT[C/T]GTTGTATGACCTCTC | 57097 |
rs3809251 | snp | C/T | 0.123105 | 0.215401 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839552 | CCTTCAAATGATCCT[C/T]CTATAATCGCTTCAA | 57097 |
rs3809252 | snp | C/T | 0.178785 | 0.239642 | intron-variant | PARP11 | GRCh38.p7 | 12:3832190 | CTGTCCCACCCAAAG[C/T]GATTTATAACAGAAA | 57097 |
rs3809253 | snp | C/T | 0.432504 | 0.170857 | intron-variant | PARP11 | GRCh38.p7 | 12:3832173 | ATTTATAACAGAAAG[C/T]TCTGAAAGGATGTTG | 57097 |
rs3809254 | snp | C/T | 0.432651 | 0.170701 | intron-variant | PARP11 | GRCh38.p7 | 12:3832100 | AGGTAAGGTGTTTTA[C/T]AGCGGAGCACACATG | 57097 |
rs3809255 | snp | A/G | 0.0973687 | 0.197999 | intron-variant | PARP11 | GRCh38.p7 | 12:3832045 | ACTTTCCTATTTTCT[A/G]TTCTCTTTTCTAATA | 57097 |
rs3816498 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3842887 | TTGTCACTTTAGTAA[A/G]CACTATAAAGCACAC | 57097 |
rs3816500 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3842851 | CAACATTTGAAATCA[A/G]ACTTATAAACTTATA | 57097 |
rs3816501 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3842518 | ACTTCGGCAACAACC[A/G]TCAAGCGTGCTGTCC | 57097 |
rs3816502 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3842512 | GCAACAACCGTCAAG[C/T]GTGCTGTCCCCTATG | 57097 |
rs3816503 | snp | A/C | 0.126564 | 0.217402 | intron-variant | PARP11 | GRCh38.p7 | 12:3842391 | GCTTGGCTGTCCTTT[A/C]CAGGACTCCTCACTT | 57097 |
rs3816506 | snp | C/T | 0.411746 | 0.190626 | intron-variant | PARP11 | GRCh38.p7 | 12:3842143 | ACTTTTTCTGTTTTT[C/T]CTTTCAGACTTTGAA | 57097 |
rs3816507 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3842058 | AATCTGAGTGGGAGG[A/G/T]TGAGCCTTTCCCTCT | 57097 |
rs3825338 | snp | A/G | 0.210909 | 0.246925 | intron-variant | PARP11 | GRCh38.p7 | 12:3814532 | GTCTCTGCAAACTTT[A/G]TATTACTTGTTTGTT | 57097 |
rs3825374 | snp | G/T | 0.416545 | 0.186448 | intron-variant | PARP11 | GRCh38.p7 | 12:3832249 | ATTTGATAAGGAATT[G/T]TATAAGATTTGAAGT | 57097 |
rs3834497 | in-del | -/T | 0.0973687 | 0.197999 | intron-variant | PARP11 | GRCh38.p7 | 12:3831281 | TTATGTGTGTATAAT[-/T]ATACACACACAAACA | 57097 |
rs4044431 | snp | A/G | 0.474 | 0.111014 | intron-variant | PARP11 | GRCh38.p7 | 12:3854310 | CCGAAGGAGATAGAG[A/G]CACAAAAAACTCTTC | 57097 |
rs4085225 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3843654 | GGTAGGTAACATCTT[A/C]CATTCTGCTTTCTTC | 57097 |
rs4085226 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3843662 | ACATCTTCCATTCTG[C/T]TTTCTTCCAGTCTTT | 57097 |
rs4556624 | snp | A/T | 0 | 0 | intron-variant | PARP11 | GRCh38.p7 | 12:3862572 | ttataaatttttcta[A/T]actatatattttatt | 57097 |
rs4765756 | snp | A/G | 0.27893 | 0.24832 | intron-variant | PARP11 | GRCh38.p7 | 12:3843275 | TTAGCACTGGTGTAA[A/G]TATCATGGTGCCTAC | 57097 |
rs4765757 | snp | C/T | 0.400682 | 0.199487 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3873541 | CGAGTCTGTGTCTGA[C/T]GAAGGAGTTTAAAGG | 57097 |
rs4766174 | snp | C/T | 0.416382 | 0.186593 | intron-variant | PARP11 | GRCh38.p7 | 12:3830533 | ACTTACTCCTGTGAA[C/T]GTGCCTGTATCTGTG | 57097 |
rs4766175 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3846779 | AAAAAAAAGAAAAGA[A/G]AAAAGAAATAGAAAA | 57097 |
rs4766178 | snp | A/T | 0.470327 | 0.118136 | intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3872115 | CTCATTCCAGAAGGG[A/T]CCTTCCTCCTCCGTA | 57097 |
rs4766179 | snp | A/G | 0.0596104 | 0.162024 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3873491 | CCTGCACGCTTATCC[A/G]TACGCGCGCGGGCGG | 57097 |
rs5796079 | in-del | -/AT | 0.461148 | 0.133852 | intron-variant | PARP11 | GRCh38.p7 | 12:3814791 | TTCACAGAGAAATGA[-/AT]ATATAGTCATGTATT | 57097 |
rs7135946 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | PARP11 | GRCh38.p7 | 12:3835460 | ttaaaatatccagtt[C/T]tcaacaaaaaaatta | 57097 |
rs7137255 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810674 | gaaggaaggaaggaa[A/G]gaaggaaggaaagaa | 57097 |
rs7137256 | snp | A/G | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810678 | gaaggaaggaaggaa[A/G]gaaggaaagaaagaa | 57097 |
rs7138053 | snp | C/T | 0.440471 | 0.161928 | intron-variant | PARP11 | GRCh38.p7 | 12:3859391 | AACACGGTGAAACCC[C/T]GTCTCTACTAAAATA | 57097 |
rs7295047 | snp | C/T | 0.491263 | 0.0655142 | intron-variant | PARP11 | GRCh38.p7 | 12:3841811 | TAATGAGGCAGAATA[C/T]TGTCCTGCCCTCTGA | 57097 |
rs7295265 | snp | A/C | 0.417359 | 0.185718 | intron-variant | PARP11 | GRCh38.p7 | 12:3836512 | atgatactaggcatt[A/C]gtaataatccatggg | 57097 |
rs7300043 | snp | A/G | 0.359152 | 0.224913 | intron-variant | PARP11 | GRCh38.p7 | 12:3849547 | CAAGTAAAATAAGCC[A/G]AGCACGGAAAGACAA | 57097 |
rs7305729 | snp | C/T | 0.375797 | 0.216044 | intron-variant | PARP11 | GRCh38.p7 | 12:3827370 | TTCCAAAAAGTGTAG[C/T]CTACTAAAAAATATT | 57097 |
rs7308098 | snp | C/T | 0.212728 | 0.247206 | intron-variant | PARP11 | GRCh38.p7 | 12:3859811 | TGGCTATACTAATGC[C/T]AGGCAAAATAGACTT | 57097 |
rs7308661 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810646 | gagggagggagggaa[A/G]gaaggaaggaaggaa | 57097 |
rs7308838 | snp | C/T | 0.424968 | 0.178567 | intron-variant | PARP11 | GRCh38.p7 | 12:3838258 | tcgtatcacttatct[C/T]ttctgaccacaatga | 57097 |
rs7309763 | snp | A/T | 0.103794 | 0.20279 | intron-variant | PARP11 | GRCh38.p7 | 12:3835616 | tgctcaaagacataa[A/T]tgaaactttgcttaa | 57097 |
rs7309844 | snp | G/T | 0.212122 | 0.247114 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3872821 | AGTGAAGGCAGTCGG[G/T]AGGCTGAGGCACGAC | 57097 |
rs7309900 | snp | C/T | 0.410905 | 0.191336 | intron-variant | PARP11 | GRCh38.p7 | 12:3835559 | atgaggcacaggtgg[C/T]agactgggcaaacaa | 57097 |
rs7310728 | snp | A/G | 0.418169 | 0.184985 | intron-variant | PARP11 | GRCh38.p7 | 12:3864040 | GCTTAAGAATGGGCA[A/G]GGTTTCAACAACCCC | 57097 |
rs7312329 | snp | C/T | 0.499923 | 0.00618962 | intron-variant | PARP11 | GRCh38.p7 | 12:3860841 | GACACCACGTCTGGC[C/T]AATTAATTTTTCAAT | 57097 |
rs7312656 | snp | C/T | 0.491834 | 0.0633738 | intron-variant | PARP11 | GRCh38.p7 | 12:3846093 | GTGTTAAAAGGAAAC[C/T]AGTACTTTATATTCT | 57097 |
rs7313046 | snp | C/T | 0.421842 | 0.181577 | intron-variant | PARP11 | GRCh38.p7 | 12:3835658 | aaattatgatgacaa[C/T]gtctcatcaaataaa | 57097 |
rs7315750 | snp | C/G | 0.0391387 | 0.134304 | intron-variant | PARP11 | GRCh38.p7 | 12:3837018 | TACCTGAAGGGAGAA[C/G]TATCCCTGAAAACAG | 57097 |
rs7315816 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | PARP11 | GRCh38.p7 | 12:3817278 | GGAGTTTCTCTTAGA[C/T]ATTATAAATAAACTG | 57097 |
rs7315970 | snp | C/G | 0.120674 | 0.21395 | intron-variant | PARP11 | GRCh38.p7 | 12:3827094 | TCATCTCAGCATGTG[C/G]AGCAAGACCTGTGAT | 57097 |
rs7488767 | snp | C/T | 0.00514135 | 0.0504405 | intron-variant | PARP11 | GRCh38.p7 | 12:3820759 | TCATCTAAACAAGAA[C/T]TAAATTAAACTGTCT | 57097 |
rs7952859 | snp | G/T | 0.122064 | 0.214785 | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3870069 | caacttaaaagttat[G/T]aattgttcatttctg | 57097 |
rs7955171 | snp | C/T | 0.482757 | 0.0912364 | intron-variant | PARP11 | GRCh38.p7 | 12:3844774 | TTTCTCAGTGACCTC[C/T]GGAATAAAAGAACTG | 57097 |
rs7955234 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3837606 | ctttataaataataa[C/T]cctgaatgcaaatgg | 57097 |
rs7955826 | snp | C/T | 0.491421 | 0.0649309 | intron-variant | PARP11 | GRCh38.p7 | 12:3845367 | ATATCTTATTTAATG[C/T]AGACTGTATTCTTGC | 57097 |
rs7956655 | snp | A/C | 0.474453 | 0.110094 | intron-variant | PARP11 | GRCh38.p7 | 12:3862928 | cctttgatttctttt[A/C]ctgggattgcattga | 57097 |
rs7956777 | snp | C/T | 0.121022 | 0.21416 | intron-variant | PARP11 | GRCh38.p7 | 12:3828132 | GACAGAAGGCAATGT[C/T]CATTAAAGAAATTGT | 57097 |
rs7958341 | snp | C/T | 0.498673 | 0.0257246 | intron-variant | PARP11 | GRCh38.p7 | 12:3823461 | ACAGTGCATAGAGAG[C/T]ATCATtattcctagt | 57097 |
rs7961501 | snp | A/G | 0.244205 | 0.249933 | intron-variant | PARP11 | GRCh38.p7 | 12:3852136 | catctataggtcacc[A/G]tcatcaaagaccaaa | 57097 |
rs7965153 | snp | A/G | 0.100588 | 0.200439 | intron-variant | PARP11 | GRCh38.p7 | 12:3849296 | ttatccagcaactcc[A/G]cgactgagtatatac | 57097 |
rs7965615 | snp | C/T | 0.4087 | 0.193169 | intron-variant | PARP11 | GRCh38.p7 | 12:3817634 | ATCCACAATCATTCC[C/T]GAACTTACTGAAAGT | 57097 |
rs7966321 | snp | C/T | 0.0547245 | 0.156101 | intron-variant | PARP11 | GRCh38.p7 | 12:3825481 | ACTACCTAATTCTTA[C/T]GGCCCCAGTAATTGT | 57097 |
rs7967785 | snp | A/G | 0.293807 | 0.246132 | intron-variant | PARP11 | GRCh38.p7 | 12:3862469 | aaaataaaTATATGT[A/G]TTtttttttctattt | 57097 |
rs7972101 | snp | A/G | 0.179744 | 0.239925 | intron-variant | PARP11 | GRCh38.p7 | 12:3822773 | TTTAAAATGTAAAGA[A/G]GATTTTAGGCAAAGA | 57097 |
rs7972536 | snp | A/G | 0.489142 | 0.0728777 | intron-variant | PARP11 | GRCh38.p7 | 12:3850797 | tgttatagcaactgg[A/G]cagcaatgttaagtc | 57097 |
rs7972649 | snp | C/T | 0.212122 | 0.247114 | intron-variant | PARP11 | GRCh38.p7 | 12:3844752 | GAGAATTTTAGCAGA[C/T]GGTACTTTTCTCAGT | 57097 |
rs7973468 | snp | C/T | 0.413582 | 0.189052 | intron-variant | PARP11 | GRCh38.p7 | 12:3845390 | ATTCTTGCAGTGTGT[C/T]GTTTCCTTTGTGACT | 57097 |
rs7973571 | snp | C/T | 0.491421 | 0.0649309 | intron-variant | PARP11 | GRCh38.p7 | 12:3845473 | GTGCAATAAAGTTCC[C/T]TTCTAACCATTTCTG | 57097 |
rs7973966 | snp | G/T | 0.375797 | 0.216044 | intron-variant | PARP11 | GRCh38.p7 | 12:3827775 | CTGGGCCTTGGTTCA[G/T]CCAAGGGGATTTCCT | 57097 |
rs7975273 | snp | A/T | 0.495634 | 0.0465208 | intron-variant | PARP11 | GRCh38.p7 | 12:3822900 | TCGATGTTCTCCAAG[A/T]TCTAACTCAAACCTA | 57097 |
rs9668244 | snp | C/G | 0.494187 | 0.0535994 | intron-variant | PARP11 | GRCh38.p7 | 12:3856714 | GGAAGATGGAAGACA[C/G]TGTGGTGATTCCTCA | 57097 |
rs10400490 | snp | C/T | 0.315758 | 0.241197 | intron-variant | PARP11 | GRCh38.p7 | 12:3860790 | CAAGTGATCCTTGTG[C/T]TTCAGCTTCCTGAGG | 57097 |
rs10437816 | snp | A/G | 0.314787 | 0.241459 | intron-variant | PARP11 | GRCh38.p7 | 12:3859165 | aaaggcatatatgaa[A/G]caaataaattcatgt | 57097 |
rs10437817 | snp | A/G | 0.314544 | 0.241524 | intron-variant | PARP11 | GRCh38.p7 | 12:3859336 | ttgcgaggccgaggc[A/G]agtggatcacaaggt | 57097 |
rs10437818 | snp | A/T | 0.314544 | 0.241524 | intron-variant | PARP11 | GRCh38.p7 | 12:3859368 | aggagatcgagacca[A/T]cttgaccaacacggt | 57097 |
rs10459122 | snp | G/T | 0.0980852 | 0.198549 | intron-variant | PARP11 | GRCh38.p7 | 12:3866757 | AAAACAGGTAAAAAT[G/T]CTTGATACTGCTGAG | 57097 |
rs10491975 | snp | A/G | 0.24019 | 0.249807 | downstream-variant-500B | PARP11 | GRCh38.p7 | 12:3808547 | CTACAGAGCTGTTCC[A/G]CTGAGCCAGGGGAGC | 57097 |
rs10491976 | snp | A/G | 0.24019 | 0.249807 | intron-variant | PARP11 | GRCh38.p7 | 12:3817707 | CTCTTAGGGACTAGA[A/G]TGCCAAACTGGCTAA | 57097 |
rs10491977 | snp | A/G | 0.12932 | 0.218944 | intron-variant | PARP11 | GRCh38.p7 | 12:3829200 | CTAAGCCAGCATATT[A/G]AAAATGGTTTAAGGA | 57097 |
rs10505726 | snp | C/T | 0.176861 | 0.239062 | intron-variant | PARP11 | GRCh38.p7 | 12:3868792 | TACACTATAACCTCC[C/T]AATTAGTCTTCCTAC | 57097 |
rs10687780 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810706 | AAGGAAGGAAGAGAG[-/A]AGAGAAGAGAAGAGA | 57097 |
rs10774174 | snp | C/T | 0.40733 | 0.194287 | intron-variant | PARP11 | GRCh38.p7 | 12:3815932 | CCTGCATTTAAATGG[C/T]GACAGAGATGAAAAC | 57097 |
rs10774175 | snp | A/G | 0.314544 | 0.241524 | intron-variant | PARP11 | GRCh38.p7 | 12:3859077 | CACTCGAGCCTGGGC[A/G]ACAGAGCAAGACTCC | 57097 |
rs10774176 | snp | A/G | 0.342134 | 0.232404 | intron-variant | PARP11 | GRCh38.p7 | 12:3859960 | TATTTGGCTGAGGAA[A/G]CCTCTAAACAATTTG | 57097 |
rs10774178 | snp | A/C | 0.403158 | 0.197592 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3874069 | AAATAATCTTCCATG[A/C]AACAAAGGATCTACC | 57097 |
rs10848940 | snp | C/G | 0.358303 | 0.225323 | intron-variant | PARP11 | GRCh38.p7 | 12:3815201 | AAAAGAATCCCCTCC[C/G]CCGGCTTCTGATAGC | 57097 |
rs10848941 | snp | A/G | 0.0973687 | 0.197999 | intron-variant | PARP11 | GRCh38.p7 | 12:3827794 | AGGGGATTTCCTAAC[A/G]TTTCACCACCCTACC | 57097 |
rs10848942 | snp | C/T | 0.499801 | 0.00998203 | intron-variant | PARP11 | GRCh38.p7 | 12:3834534 | AGCTACTCAGGAGGC[C/T]GAGAGAAGAGAACTG | 57097 |
rs10848943 | snp | A/G | 0.493793 | 0.055364 | intron-variant | PARP11 | GRCh38.p7 | 12:3834856 | TGATCAGGGCAGAAC[A/G]TGGGGCAGTCTTGAA | 57097 |
rs10848944 | snp | C/T | 0.39121 | 0.2063 | intron-variant | PARP11 | GRCh38.p7 | 12:3846994 | AGGTGGGAGTATCAC[C/T]TGAGCTCTGGCAGTT | 57097 |
rs10848945 | snp | A/G | 0.488726 | 0.0742286 | intron-variant | PARP11 | GRCh38.p7 | 12:3848378 | AGCAAAAATAAGGCT[A/G]GAGGCCTCACATTAC | 57097 |
rs10848946 | snp | C/G | 0.357664 | 0.225629 | intron-variant | PARP11 | GRCh38.p7 | 12:3854229 | CAATTAAAAGAACTA[C/G]AGAAGCAAGAGCAAA | 57097 |
rs10848948 | snp | A/G | 0.22263 | 0.248497 | intron-variant | PARP11 | GRCh38.p7 | 12:3863684 | CAAGCGTCCCTTCCC[A/G]GTGCAGTCACATGGG | 57097 |
rs11062836 | snp | G/T | 0.128976 | 0.218754 | downstream-variant-500B | PARP11 | GRCh38.p7 | 12:3808490 | GGCTGGAGGTTAGAT[G/T]GGCTGTAGGAAGGAT | 57097 |
rs11062837 | snp | C/T | 0.128976 | 0.218754 | downstream-variant-500B | PARP11 | GRCh38.p7 | 12:3808546 | CCTACAGAGCTGTTC[C/T]GCTGAGCCAGGGGAG | 57097 |
rs11062838 | snp | C/T | 0.331642 | 0.236293 | downstream-variant-500B | PARP11 | GRCh38.p7 | 12:3808716 | GAGACTTCCCCCATC[C/T]GCAAGTGGGGTACAT | 57097 |
rs11062839 | snp | A/G | 0.129664 | 0.219133 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3809996 | TACCTCCCACTGCAC[A/G]ATTACACATATGCTG | 57097 |
rs11062841 | snp | C/T | 0.364817 | 0.222075 | intron-variant | PARP11 | GRCh38.p7 | 12:3813100 | GTGAGCCACCATGCC[C/T]GGCCCTGAGTTTTAC | 57097 |
rs11062842 | snp | C/T | 0.12932 | 0.218944 | intron-variant | PARP11 | GRCh38.p7 | 12:3813263 | ACCGTATTTCTATGA[C/T]ATGGGATAACAATTC | 57097 |
rs11062843 | snp | A/T | 0.12932 | 0.218944 | intron-variant | PARP11 | GRCh38.p7 | 12:3819008 | CCACATTTTCTAACA[A/T]CTCCAAAACCTTTGT | 57097 |
rs11062844 | snp | C/T | 0.408871 | 0.193029 | intron-variant | PARP11 | GRCh38.p7 | 12:3819304 | GGTCAGGCAACCCAA[C/T]GTGTCTCAGTTTAAT | 57097 |
rs11062846 | snp | C/T | 0.41833 | 0.184838 | intron-variant | PARP11 | GRCh38.p7 | 12:3823554 | ATTCTATTTTACAGA[C/T]GCACAGAACTCCGCC | 57097 |
rs11062850 | snp | A/C | 0.0973687 | 0.197999 | intron-variant | PARP11 | GRCh38.p7 | 12:3825654 | AAAGGATAACATGAA[A/C]GGAAGCACTTAGAGT | 57097 |
rs11062851 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | PARP11 | GRCh38.p7 | 12:3826315 | TTAATAGCCACGCTA[C/T]GCGATGATCAGGAAT | 57097 |
rs11062852 | snp | G/T | 0.121369 | 0.214369 | intron-variant | PARP11 | GRCh38.p7 | 12:3827466 | GAGGTCTGGTGTCTG[G/T]GCATATCATTCGGTT | 57097 |
rs11062853 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3828083 | TTCCAGATTATCTGG[C/T]TAATCTGTGGAAGAG | 57097 |
rs11062854 | snp | A/C | 0.0205511 | 0.0992634 | intron-variant | PARP11 | GRCh38.p7 | 12:3832557 | CTCTGGGTTTCTTTA[A/C]AAAGATGCATTTTAT | 57097 |
rs11062855 | snp | C/G | 0.118235 | 0.212457 | intron-variant | PARP11 | GRCh38.p7 | 12:3838569 | AAAGCAAAAATAAAC[C/G]AAATCCAAAATTAAC | 57097 |
rs11062857 | snp | A/G | 0.103438 | 0.202533 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839935 | GACAGCTGCAAGAGT[A/G]AAACTGCTGTTGCTG | 57097 |
rs11062858 | snp | C/G | 0.122064 | 0.214785 | intron-variant | PARP11 | GRCh38.p7 | 12:3841956 | CCCTGAAGCAAGTGT[C/G]AGCAGTAAGCCAGAC | 57097 |
rs11062859 | snp | C/T | 0.118235 | 0.212457 | intron-variant | PARP11 | GRCh38.p7 | 12:3842028 | TATGGCATTGGCTTC[C/T]ATCCCTCCTGTAGCA | 57097 |
rs11062860 | snp | A/T | 0.0444908 | 0.142359 | intron-variant | PARP11 | GRCh38.p7 | 12:3842986 | ATTATGCAATGCCTT[A/T]GTCATAAACTGGGCT | 57097 |
rs11062861 | snp | C/T | 0.128976 | 0.218754 | intron-variant | PARP11 | GRCh38.p7 | 12:3843522 | ACACTTGCATGTTCT[C/T]CTTGTCAGGGCTGGA | 57097 |
rs11062862 | snp | C/T | 0.128976 | 0.218754 | intron-variant | PARP11 | GRCh38.p7 | 12:3843732 | GTCCTCATTTGGAGA[C/T]TGAACTCTGAATTAA | 57097 |
rs11062863 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | PARP11 | GRCh38.p7 | 12:3843940 | ACACCTAGCCAAAAC[C/T]AGATGCGGTGACTTT | 57097 |
rs11062864 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | PARP11 | GRCh38.p7 | 12:3845020 | CTGAGGATCATTTGC[A/C]TTTTTGAGTTGGAAA | 57097 |
rs11062865 | snp | C/T | 0.128976 | 0.218754 | intron-variant | PARP11 | GRCh38.p7 | 12:3845307 | CCTAAGCTCAGACCC[C/T]GCCTTGTCCTGGCAA | 57097 |
rs11062866 | snp | A/G | 0.275999 | 0.248644 | intron-variant | PARP11 | GRCh38.p7 | 12:3846584 | ACACGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 57097 |
rs11062867 | snp | C/T | 0.095934 | 0.196885 | intron-variant | PARP11 | GRCh38.p7 | 12:3846673 | GAATCAGGAAAATGG[C/T]GTGAACCCAGGAGGC | 57097 |
rs11062869 | snp | A/G | 0.357664 | 0.225629 | intron-variant | PARP11 | GRCh38.p7 | 12:3853436 | AATAAAGGGATGGAG[A/G]AAGATCTACCAAGCA | 57097 |
rs11062870 | snp | A/G | 0.357664 | 0.225629 | intron-variant | PARP11 | GRCh38.p7 | 12:3854301 | AGAGCAGAACCGAAG[A/G]AGATAGAGGCACAAA | 57097 |
rs11062871 | snp | C/T | 0.0980852 | 0.198549 | intron-variant | PARP11 | GRCh38.p7 | 12:3855680 | AGGAAGAATCAATAT[C/T]GTGAAAATGGCCATA | 57097 |
rs11062873 | snp | A/G | 0.409721 | 0.192325 | intron-variant | PARP11 | GRCh38.p7 | 12:3856796 | TATACCCAAAGGATT[A/G]TAAATCATGCTACTA | 57097 |
rs11062874 | snp | A/G | 0.317692 | 0.240661 | intron-variant | PARP11 | GRCh38.p7 | 12:3860050 | CTTAAAGACAGAATT[A/G]TTAAGCAAAAAAGAA | 57097 |
rs11062875 | snp | C/T | 0.313814 | 0.241719 | intron-variant | PARP11 | GRCh38.p7 | 12:3861196 | AAGACACAAATTTTT[C/T]GTGGAGGGAAGGGCC | 57097 |
rs11062876 | snp | C/T | 0.147656 | 0.228091 | intron-variant | PARP11 | GRCh38.p7 | 12:3862940 | TTTCCTGGGATTGCA[C/T]TGAATTATCAATCTG | 57097 |
rs11062877 | snp | A/G | 0.129664 | 0.219133 | intron-variant | PARP11 | GRCh38.p7 | 12:3863156 | GCATTTTAAAAGTCA[A/G]TTTCTGATTATATGT | 57097 |
rs11062878 | snp | C/T | 0.129664 | 0.219133 | intron-variant | PARP11 | GRCh38.p7 | 12:3865482 | AGTTAACTGGGTATC[C/T]TTCTATTTCTTATTG | 57097 |
rs11062884 | snp | C/T | 0.126909 | 0.217598 | intron-variant | PARP11 | GRCh38.p7 | 12:3868546 | ttccaaactttacta[C/T]ctgatgcttcatagg | 57097 |
rs11062885 | snp | A/C | 0.275732 | 0.248672 | intron-variant | PARP11 | GRCh38.p7 | 12:3869495 | TCTGGTGCACTGTGT[A/C]CCAGCCACATAGGCT | 57097 |
rs11062886 | snp | C/T | 0.277334 | 0.248501 | intron-variant, nc-transcript-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3871790 | gctcagaaaatacta[C/T]cccgaagtatgacac | 57097 |
rs11062887 | snp | A/C | 0.130008 | 0.219321 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3875171 | ATAGGTTTGCATAAT[A/C]CTTGGGAAGTTTGTT | 57097 |
rs11275972 | in-del | -/TATATTATCATGC | 0.476314 | 0.106217 | intron-variant | PARP11 | GRCh38.p7 | 12:3866856 | TTCTACTGGATGTCA[-/TATATTATCATGC]TATATTATCATGCAA | 57097 |
rs11283159 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810717 | AGAGAGAGAGAAGAG[-/A]AAGAGAAAGAGAAAG | 57097 |
rs11376275 | in-del | -/T | 0.497749 | 0.0334707 | intron-variant | PARP11 | GRCh38.p7 | 12:3865889 | TGCTTTTTTTTTTTT[-/T]GGTCCCACCTGTTCT | 57097 |
rs11503117 | snp | G/T | 0.0205511 | 0.0992634 | intron-variant | PARP11 | GRCh38.p7 | 12:3855509 | GAGCCAAATCATGAG[G/T]GAACTCCCATTCACA | 57097 |
rs11513711 | snp | C/T | 0.127254 | 0.217792 | intron-variant | PARP11 | GRCh38.p7 | 12:3851847 | AGCTTAACTGGGAGA[C/T]ACCTCCCAGTAGGGG | 57097 |
rs11519560 | snp | C/T | 0.126909 | 0.217598 | intron-variant | PARP11 | GRCh38.p7 | 12:3853797 | GACCTAATAGACATC[C/T]ACAGAACTCTCCACC | 57097 |
rs11519571 | snp | C/G | 0.127944 | 0.218179 | intron-variant | PARP11 | GRCh38.p7 | 12:3863096 | AAATCTTTTATGCTA[C/G]TTTCAGGCTTATTTC | 57097 |
rs11532328 | snp | A/G | 0.100944 | 0.200705 | intron-variant | PARP11 | GRCh38.p7 | 12:3849075 | ATGCTCAAAATCACT[A/G]ATTTTCAGAGAAATG | 57097 |
rs11609162 | snp | C/G | | | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839480 | TGCACTCTCAGTCTC[C/G]CCATGTTGAAGTCAG | 57097 |
rs11609962 | snp | G/T | 0.00930212 | 0.0675613 | intron-variant | PARP11 | GRCh38.p7 | 12:3843077 | TCATCTCGATATCTG[G/T]CAAACTTGAATAATG | 57097 |
rs11612988 | snp | C/G | 0.240478 | 0.249819 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810886 | aaaaTCAATGTGAGA[C/G]ACTCTTCACCATCAC | 57097 |
rs11613447 | snp | A/G | 0.407845 | 0.193868 | intron-variant | PARP11 | GRCh38.p7 | 12:3817135 | GGCGGAACTTGCAGT[A/G]AGCTGAGATCGCGCC | 57097 |
rs11616103 | snp | G/T | 0.247621 | 0.249989 | intron-variant | PARP11 | GRCh38.p7 | 12:3862147 | AAAAGATTTTTCTCa[G/T]ccaggcatagtggct | 57097 |
rs11829684 | snp | C/T | 0.0260105 | 0.111035 | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3870687 | TCTAGTTGAAGATAC[C/T]ATAGGAAAAATAACA | 57097 |
rs11831681 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | PARP11 | GRCh38.p7 | 12:3850294 | cataatatatatAGC[A/C]TAATTATATcagttc | 57097 |
rs11832674 | snp | A/G | 0.0283406 | 0.115616 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3873320 | TTCCTGCGGGTCCCC[A/G]GGAGCGAAGGGACGG | 57097 |
rs11837745 | snp | G/T | 0.0260105 | 0.111035 | intron-variant | PARP11 | GRCh38.p7 | 12:3869090 | ctctttgaccattct[G/T]ccatagtcactccat | 57097 |
rs11838161 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | PARP11 | GRCh38.p7 | 12:3861751 | tctttgtggccaggc[A/G]tggtggctcacgcct | 57097 |
rs12228457 | snp | A/G | 0.097727 | 0.198275 | intron-variant | PARP11 | GRCh38.p7 | 12:3845572 | ATTTTTAGATGAGGT[A/G]AATGTTTTGTCTTTT | 57097 |
rs12296366 | snp | G/T | 0.426354 | 0.177198 | intron-variant | PARP11 | GRCh38.p7 | 12:3822464 | attagccaggcgtgg[G/T]ggcgggcgcctgtag | 57097 |
rs12297359 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | PARP11 | GRCh38.p7 | 12:3862721 | ttttcccactgaatC[A/G]Taccttttaaaaaat | 57097 |
rs12304518 | snp | C/T | 0.364401 | 0.222289 | intron-variant | PARP11 | GRCh38.p7 | 12:3813669 | TTCTCTTGCTGGAAG[C/T]AAGGTACAAAGTAAG | 57097 |
rs12304669 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | PARP11 | GRCh38.p7 | 12:3835175 | GCCACCAAGCCACAC[A/G]CACATTTAACACTTA | 57097 |
rs12305957 | snp | C/T | 0.16028 | 0.233346 | intron-variant | PARP11 | GRCh38.p7 | 12:3834922 | AGCGGAGAAACTTCA[C/T]TGGCACAAGGGTCTG | 57097 |
rs12309075 | snp | C/T | 0.152001 | 0.229992 | intron-variant | PARP11 | GRCh38.p7 | 12:3837350 | aaagatactcaacag[C/T]taaattacaaagatc | 57097 |
rs12309614 | snp | A/C | 0.316726 | 0.240931 | intron-variant | PARP11 | GRCh38.p7 | 12:3862325 | gggcatggtagcatg[A/C]acctgtagtcccagc | 57097 |
rs12315370 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | PARP11 | GRCh38.p7 | 12:3852879 | tgttaagggcagcca[C/G]agagaaaggtcaggt | 57097 |
rs12316120 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3837430 | agtcttgcggtaacc[A/G]taatgcaaaaaccta | 57097 |
rs12317047 | snp | A/G | 0.432797 | 0.170544 | intron-variant | PARP11 | GRCh38.p7 | 12:3822371 | TGGGAGGCCGAGGCG[A/G]GCGGATCACGAGGTC | 57097 |
rs12317099 | snp | A/G | 0.426047 | 0.177503 | intron-variant | PARP11 | GRCh38.p7 | 12:3822456 | acaaaaaaattagcc[A/G]ggcgtgggggcgggc | 57097 |
rs12319851 | snp | A/G | 0.481396 | 0.0946345 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839384 | CGCCCATGGACGCCT[A/G]TCTGCGGAAACTGGG | 57097 |
rs12320803 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | PARP11 | GRCh38.p7 | 12:3868610 | ctgttatcttccATA[C/T]GGCTCAGTGAAAACA | 57097 |
rs12322468 | snp | A/C | 0.402982 | 0.197728 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3874420 | TGCGCCACCACGTCC[A/C]GCGAATTTTTGTATT | 57097 |
rs12369729 | snp | C/T | 0.128976 | 0.218754 | intron-variant | PARP11 | GRCh38.p7 | 12:3822515 | GAGGCAGGAGAATGG[C/T]GTGAACCCGGGAGGC | 57097 |
rs12370945 | snp | A/G | 0.413083 | 0.189483 | intron-variant | PARP11 | GRCh38.p7 | 12:3856415 | aaagaactcaaacaa[A/G]tttacaagaaaaaaa | 57097 |
rs12371001 | snp | C/T | 0.129664 | 0.219133 | intron-variant | PARP11 | GRCh38.p7 | 12:3824750 | AGCAGATACAATGTA[C/T]AATTACAATAACATC | 57097 |
rs12424076 | snp | C/T | 0.24019 | 0.249807 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810503 | gctgaggcaagagaa[C/T]tgcttgaacccggga | 57097 |
rs12424633 | snp | C/T | 0.406986 | 0.194565 | intron-variant | PARP11 | GRCh38.p7 | 12:3816060 | ATGACATCAGAAGGT[C/T]GTGCATTTAGCAAAT | 57097 |
rs12426410 | snp | A/T | 0.241053 | 0.24984 | intron-variant | PARP11 | GRCh38.p7 | 12:3827028 | GTCCTTTCTGTGTTC[A/T]CCTAGACTCTACACA | 57097 |
rs12579394 | snp | C/T | 0.213333 | 0.247296 | intron-variant | PARP11 | GRCh38.p7 | 12:3849053 | ttgccaacaggtata[C/T]gagaaaatgctcaaa | 57097 |
rs12581274 | snp | C/T | 0.204496 | 0.245824 | intron-variant, utr-variant-5-prime | PARP11 | GRCh38.p7 | 12:3863956 | tcgggcatgcaaata[C/T]actattaagacaaaa | 57097 |
rs12582206 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PARP11 | GRCh38.p7 | 12:3821625 | CTCTGTAATGCTGAT[C/T]TCAGCCAAGATGCAT | 57097 |
rs12582916 | snp | A/C | 0 | 0 | intron-variant | PARP11 | GRCh38.p7 | 12:3830475 | TGAGTGTAAAAGATT[A/C]CAAAAAAATAGAAAT | 57097 |
rs12823996 | snp | C/T | 0.16618 | 0.23553 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3873309 | GATTTTTTTTTTTCC[C/T]GCGGGTCCCCGGGAG | 57097 |
rs12824604 | snp | A/G | 0.172674 | 0.237741 | intron-variant | PARP11 | GRCh38.p7 | 12:3851587 | tgctgaggcttgagt[A/G]ggtaaacaaagtggc | 57097 |
rs16930824 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PARP11 | GRCh38.p7 | 12:3823031 | GTTCAAGCCACCCGA[C/T]GTGAATACAGAAAAA | 57097 |
rs16930833 | snp | A/G | 0.0543475 | 0.155628 | intron-variant | PARP11 | GRCh38.p7 | 12:3824946 | TAAGTACTTGGAATA[A/G]CTTTTATATCGTGAT | 57097 |
rs16930856 | snp | A/G | 0.111079 | 0.207848 | intron-variant | PARP11 | GRCh38.p7 | 12:3845975 | TGTGTATGAAAAACG[A/G]TAATAGCCTTACACT | 57097 |
rs17698952 | snp | C/T | 0.140581 | 0.224783 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3874562 | TCTTGCACCCGGCCA[C/T]ATTTTAAAGTAGACT | 57097 |
rs17836424 | snp | G/T | 0.128632 | 0.218563 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3873055 | CCACTGCTTAAAAAG[G/T]TACAGACTACAGAAG | 57097 |
rs34027116 | in-del | -/A | | | intron-variant | PARP11 | GRCh38.p7 | 12:3859819 | TAATGCCAGGCAAAA[-/A]TAGACTTCAAACCAA | 57097 |
rs34137558 | in-del | -/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3838151 | TCAATTGCTGGAGAA[-/T]ACACATTCTTTTCAT | 57097 |
rs34194608 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3857508 | TTACAGGAATTAAGG[A/G]TGCCAAAGACAGAAT | 57097 |
rs34240863 | in-del | -/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3835397 | CATAAACCAATAACC[-/C]AAACAAACAACCACA | 57097 |
rs34406933 | in-del | -/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3817456 | GTGCCCACTACTCCC[-/C]ACTACTAAGGCAGCC | 57097 |
rs34515229 | in-del | -/T | | | utr-variant-5-prime, frameshift-variant, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3829915 | GCCACTTCCCACATT[-/T]CTGCCAAGTAAAACC | 57097 |
rs34623922 | in-del | -/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3838442 | AATCTATGGGATACA[-/G]ACAAAAGCAGTACTA | 57097 |
rs34628311 | in-del | -/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3822646 | ATGTGTGCTACTTTT[-/T]AGGTGTTCAATAGTG | 57097 |
rs34712844 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3857979 | TTCAAAAGTAGTTTA[G/T]CATGGAGGATGCCAC | 57097 |
rs34734765 | in-del | -/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3816077 | GCATTTAGCAAATGT[-/G]TTACTTTACAAAAAG | 57097 |
rs34818389 | in-del | -/T | 0.473909 | 0.111197 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3809021 | AAAGATTTATGAAAC[-/T]TTTTTTTTTACCCTG | 57097 |
rs34829083 | in-del | -/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3864018 | AAAGGACAGTCATGG[-/G]AAACAAGCTTAAGAA | 57097 |
rs34830185 | in-del | -/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3864780 | CTTAATATTGGTAAT[-/G]TTGTGTCTTCTTTTT | 57097 |
rs34905595 | in-del | -/AT | | | intron-variant | PARP11 | GRCh38.p7 | 12:3814792 | TCACAGAGAAATGAA[-/AT]TATAGTCATGTATTT | 57097 |
rs34964628 | in-del | -/A | 0.229136 | 0.249128 | intron-variant | PARP11 | GRCh38.p7 | 12:3837666 | GAAGAAAAAAAAAAA[-/A]CCAAGATCCAAATAT | 57097 |
rs34988365 | in-del | -/G | | | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3873142 | GGGAAGCAGTTCCGG[-/G]TGACCCCCTCCCGCC | 57097 |
rs35109385 | in-del | -/A | 0.210909 | 0.246925 | intron-variant | PARP11 | GRCh38.p7 | 12:3816205 | AAAGTTTTTTAAATT[-/A]AAAAAAGAAGATAAT | 57097 |
rs35187076 | in-del | -/A | | | intron-variant | PARP11 | GRCh38.p7 | 12:3829154 | TACTAATCACCTGTT[-/A]CTAGTTCCCAACACA | 57097 |
rs35235857 | in-del | -/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3833357 | TTATCCCAGGGCTTT[-/T]GGTGAGGCTGAGAAG | 57097 |
rs35243468 | in-del | -/A | | | intron-variant | PARP11 | GRCh38.p7 | 12:3835864 | AAAGGAAAGAAAAAA[-/A]TTGCAGAAAAATAAA | 57097 |
rs35267321 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PARP11 | GRCh38.p7 | 12:3828223 | CCAGCTACCTATGAC[C/T]TTCTCACTTAACATC | 57097 |
rs35288911 | in-del | -/C | | | splice-acceptor-variant | PARP11 | GRCh38.p7 | 12:3830019 | TTGTGAAACATCTCC[-/C]TGAAAAGCCAGAAGG | 57097 |
rs35494376 | in-del | -/A | | | intron-variant | PARP11 | GRCh38.p7 | 12:3867887 | CTGAAAGAGCACAAG[-/A]ATATAATCTTCAGGG | 57097 |
rs35531745 | in-del | -/T | | | frameshift-variant, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3814187 | TGAGCTGAGCCTTTT[-/T]CCTAAAAACACAATA | 57097 |
rs35597299 | in-del | -/A | | | intron-variant | PARP11 | GRCh38.p7 | 12:3862419 | CACACCACTGCACTA[-/A]CAGCCTAGGCAACCA | 57097 |
rs35605007 | in-del | -/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3817601 | AGTTCTTCACAACCC[-/C]TGCCCACCTTTGCCC | 57097 |
rs35718485 | in-del | -/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3868741 | CTTCATACTTTCCCC[-/C]ACATAGTCCAAGTCA | 57097 |
rs35805726 | in-del | -/T | 0.240765 | 0.249829 | intron-variant | PARP11 | GRCh38.p7 | 12:3823512 | ATAGTACACACTCAG[-/T]TAAGTACTGGATGAA | 57097 |
rs35806851 | in-del | -/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3833402 | GGCCAGGAGTTTGAG[-/G]CAAGCCTGGCAACAC | 57097 |
rs35843043 | in-del | -/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3814955 | GTATACATACACAGG[-/G]TAGTAAAAAATACAA | 57097 |
rs36063504 | in-del | -/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3858703 | TGATAAAGGTATTTT[-/T]GGTGATGCTATTGCA | 57097 |
rs36072906 | in-del | -/A/AA | | | intron-variant | PARP11 | GRCh38.p7 | 12:3817190 | TCAAAAAAAAAAAAA[-/A/AA]TTCATTTATCACTAC | 57097 |
rs36089402 | in-del | -/A | 0.5 | 0 | intron-variant | PARP11 | GRCh38.p7 | 12:3822617 | AAAAAAAAAAAAAAA[-/A]TTATTGACTGTCTAT | 57097 |
rs55633163 | snp | C/T | 0.15698 | 0.23205 | intron-variant | PARP11 | GRCh38.p7 | 12:3846788 | AAAAGAAAAAAGAAA[C/T]AGAAAACTTGAATAG | 57097 |
rs55751831 | snp | A/T | 0.103082 | 0.202275 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3840332 | TGTCAGGGAAGAAGA[A/T]GAAAAAACCTTCCAC | 57097 |
rs55807338 | snp | C/T | 0.122064 | 0.214785 | intron-variant | PARP11 | GRCh38.p7 | 12:3846716 | GAGCCAAGATTGCGC[C/T]ACTGCACTCCAGCCT | 57097 |
rs56723889 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | PARP11 | GRCh38.p7 | 12:3832400 | AGCAGTACAGAGAAT[A/G]TTAAAGCAACACCTA | 57097 |
rs56793596 | snp | C/T | 0.162253 | 0.234095 | intron-variant | PARP11 | GRCh38.p7 | 12:3816260 | TCTTCCAAGGTCTTT[C/T]TGACTGCTGATTCAC | 57097 |
rs56942603 | snp | C/T | 0.216048 | 0.247684 | intron-variant | PARP11 | GRCh38.p7 | 12:3866519 | GATTAATAATTTGTA[C/T]GAAAATCACTTTATT | 57097 |
rs57062061 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810700 | AAGAAAGAAGGAAGG[A/G]AGAGAGAGAGAAGAG | 57097 |
rs57172968 | in-del | -/GGA | | | cds-indel, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810678 | GAAGGAAGGAAGGAA[-/GGA]AGGAAAGAAAGAAGG | 57097 |
rs57460078 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810690 | GAAGGAAGGAAAGAA[A/G]GAAGGAAGGAAGAGA | 57097 |
rs57860326 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810699 | AAAGAAAGAAGGAAG[A/G]AAGAGAGAGAGAAGA | 57097 |
rs58303768 | in-del | -/A | | | intron-variant | PARP11 | GRCh38.p7 | 12:3823931 | AAAAAAAAAAAAAAA[-/A]TGCTACAGGAACACA | 57097 |
rs58364151 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PARP11 | GRCh38.p7 | 12:3835010 | TCCTATGAAGCCAGG[A/G]TTAAATGAAACAGCA | 57097 |
rs58512506 | snp | A/C | 0.150667 | 0.229419 | intron-variant | PARP11 | GRCh38.p7 | 12:3815192 | TAAAAATTAAAAAGA[A/C]TCCCCTCCCCCGGCT | 57097 |
rs58675636 | snp | A/G | 0.161596 | 0.233848 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810788 | GAGAGGAAGAGAAGA[A/G]GAAGAGGAAGACAGA | 57097 |
rs59300625 | in-del | -/G | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810682 | GAAGGAAGGAAGGAA[-/G]GAAAGAAAGAAGGAA | 57097 |
rs59321607 | in-del | -/AA | | | intron-variant | PARP11 | GRCh38.p7 | 12:3859576 | AAAAAAAAAAAAAAA[-/AA]GGCAGATGTAAATAA | 57097 |
rs59468704 | in-del | -/GAAA | | | intron-variant | PARP11 | GRCh38.p7 | 12:3846782 | AAAAGAAAAGAAAAA[-/GAAA]AGAAATAGAAAACTT | 57097 |
rs59836757 | snp | C/T | 0.128976 | 0.218754 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839453 | TGTTCCGGGCCGTGG[C/T]GGAGCAGGTATTGCA | 57097 |
rs60246543 | snp | A/G | 0.0980852 | 0.198549 | intron-variant | PARP11 | GRCh38.p7 | 12:3861482 | TATCTTCTTTGGTGC[A/G]GTGTCTATTCATATC | 57097 |
rs60554748 | in-del | -/T | 0.433527 | 0.169758 | intron-variant | PARP11 | GRCh38.p7 | 12:3866660 | TAAACTTTCAGATTA[-/T]TTTTCACACAAAGCA | 57097 |
rs60668774 | in-del | -/CCA | | | intron-variant | PARP11 | GRCh38.p7 | 12:3845049 | AATTATGAAACTTCA[-/CCA]TATTATGATCATACA | 57097 |
rs61283852 | in-del | -/A | 0.0995161 | 0.199636 | intron-variant | PARP11 | GRCh38.p7 | 12:3836326 | CAAAATACATAAAGT[-/A]AAAAACAAACAAAAA | 57097 |
rs61600993 | snp | A/G | 0.132066 | 0.220435 | intron-variant | PARP11 | GRCh38.p7 | 12:3816419 | CGAGTTACTCTTTGC[A/G]TAAGACTTTTTGTCT | 57097 |
rs61907081 | snp | A/G | 0.5 | 0 | intron-variant | PARP11 | GRCh38.p7 | 12:3818780 | GTATGTAATCGTACA[A/G]ATGGCACCTACTTGT | 57097 |
rs61907082 | snp | A/T | 0.5 | 0 | intron-variant | PARP11 | GRCh38.p7 | 12:3822619 | AAAAAAAAAAAAAAT[A/T]ATTGACTGTCTATGT | 57097 |
rs61907083 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | PARP11 | GRCh38.p7 | 12:3830379 | GACCCATGCTATCAC[A/G]CTGGTTAAGATCAAA | 57097 |
rs61907084 | snp | A/G | 0.154329 | 0.23097 | intron-variant | PARP11 | GRCh38.p7 | 12:3834010 | ACACAGCCCCCATTC[A/G]AAAGGTAGAATTTCT | 57097 |
rs61907099 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | PARP11 | GRCh38.p7 | 12:3841143 | GCCTTTGCCTCAGAC[A/G]TTGAGCCTTTATCAA | 57097 |
rs61907100 | snp | A/G | 0.030665 | 0.119967 | intron-variant | PARP11 | GRCh38.p7 | 12:3855721 | TAATTTATAGATTCA[A/G]TGCCATCCCCATCAA | 57097 |
rs61907101 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3856791 | GGGTATATACCCAAA[A/G]GATTATAAATCATGC | 57097 |
rs61907102 | snp | A/T | 0.5 | 0 | intron-variant | PARP11 | GRCh38.p7 | 12:3858926 | GAAACTCCATCTCTA[A/T]TTAAAAAAAAAAATA | 57097 |
rs66471305 | snp | A/G | 0.144296 | 0.226554 | intron-variant | PARP11 | GRCh38.p7 | 12:3835951 | AGTATCAGAAGCGGA[A/G]GAGAGAGAAAAAGGC | 57097 |
rs66847009 | snp | C/T | 0.0539704 | 0.155153 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3873316 | TTTTTTCCCGCGGGT[C/T]CCCGGGAGCGAAGGG | 57097 |
rs67009183 | snp | A/C | 0.162581 | 0.234218 | intron-variant | PARP11 | GRCh38.p7 | 12:3819867 | CCATTCTAGCCTCCT[A/C]TCTCACCATTCTACC | 57097 |
rs71061134 | in-del | -/A | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3809556 | GTTTTTCTTTTAGAC[-/A]TTTGCAGATCTTATC | 57097 |
rs71061135 | in-del | -/TTCCTTCC | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810678 | TCCTTCCTTCTTTCT[-/TTCCTTCC]TTCCTTCCTTCCTTC | 57097 |
rs71061136 | in-del | -/T | | | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3875136 | TTTTTTTTTTTTTTT[-/T]ACAGATGCTGATGCA | 57097 |
rs71458076 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | PARP11 | GRCh38.p7 | 12:3814607 | TTATCCTCAGAAACT[A/G]GAAAATGTTGGTTCA | 57097 |
rs71458077 | snp | G/T | 0.5 | 0 | intron-variant | PARP11 | GRCh38.p7 | 12:3865920 | CCCACCTGTTCTTTG[G/T]TCTCTTTTTTTTCTA | 57097 |
rs71534267 | in-del | -/T | 0.994286 | 0.0199822 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3873296 | GGCCTGGGTGTTGGA[-/T]TTTTTTTTTTCCCGC | 57097 |
rs71534270 | snp | A/C | 0.0154538 | 0.0865337 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PARP11 | GRCh38.p7 | 12:3811494 | TCAAGTCTGAGGCTG[A/C]AGCCTGCTATCCTAA | 57097 |
rs71583749 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3813719 | CATCCCATACCTTTT[C/T]CCCTCACCTCTCTCC | 57097 |
rs71881136 | in-del | -/TGTTA | 0.39009 | 0.207062 | intron-variant | PARP11 | GRCh38.p7 | 12:3835372 | GTTCAGCTATATCAC[-/TGTTA]TATACACATAAACCA | 57097 |
rs72516364 | in-del | -/AA/TA | | | intron-variant | PARP11 | GRCh38.p7 | 12:3814795 | CAGAGAAATGWATAT[-/AA/TA]AGTCATGTATTTACA | 57097 |
rs73045055 | snp | A/G | 0.135825 | 0.222405 | intron-variant | PARP11 | GRCh38.p7 | 12:3821107 | TTGAATCAGGATGAC[A/G]GATACATGAGGTTCA | 57097 |
rs73045058 | snp | C/T | 0.103794 | 0.20279 | intron-variant | PARP11 | GRCh38.p7 | 12:3823173 | CTTTTTTCAAACTTA[C/T]TTTAATGAAAAAAAT | 57097 |
rs73045063 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | PARP11 | GRCh38.p7 | 12:3832287 | TTTTTTTCGTCCACA[A/T]TCCAATGTGCAGGAG | 57097 |
rs73045065 | snp | C/T | 0.0513262 | 0.151752 | intron-variant | PARP11 | GRCh38.p7 | 12:3832565 | TTCTTTAAAAAGATG[C/T]ATTTTATAAGATTAA | 57097 |
rs73045090 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3861250 | ACGTTTGTGTCCTTG[A/C]CAAATTATTATGTTG | 57097 |
rs73045099 | snp | C/T | 0.0930568 | 0.194599 | intron-variant | PARP11 | GRCh38.p7 | 12:3863010 | AACCCATGAATAAAT[C/T]ATATCTTTCGACTTA | 57097 |
rs73047303 | snp | A/G | 0.114036 | 0.209795 | intron-variant | PARP11 | GRCh38.p7 | 12:3867907 | AATCTTCAGGGAGAA[A/G]TCTTCCGATAATTTT | 57097 |
rs73251454 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | PARP11 | GRCh38.p7 | 12:3817818 | CACCTGTCATCCTGC[G/T]GAACATCAGAGCCAC | 57097 |
rs73251457 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | PARP11 | GRCh38.p7 | 12:3819459 | GTTTAGCATCCTGGC[C/T]TCTATCCAGTAGATG | 57097 |
rs73251458 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | PARP11 | GRCh38.p7 | 12:3823536 | GGATGAATGAATGAA[C/T]GCATTCTATTTTACA | 57097 |
rs73251459 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | PARP11 | GRCh38.p7 | 12:3824871 | GAATGTGGATATGAC[A/G]TAGCTAGTAAGGAAA | 57097 |
rs73251463 | snp | G/T | 0.0513262 | 0.151752 | intron-variant | PARP11 | GRCh38.p7 | 12:3826290 | ACTGTACTATAAAGT[G/T]TCATGAAGATTAATA | 57097 |
rs73251465 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | PARP11 | GRCh38.p7 | 12:3832281 | ACACTATTTTTTTCG[C/T]CCACAATCCAATGTG | 57097 |
rs73251473 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | PARP11 | GRCh38.p7 | 12:3834719 | GAGCTCCAATATAAG[C/T]AGAAAGGCAGAGCAA | 57097 |
rs73251490 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | PARP11 | GRCh38.p7 | 12:3849946 | GAAAATATGTATATC[A/G]ATTATGTATCAACTT | 57097 |
rs73251499 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | PARP11 | GRCh38.p7 | 12:3863783 | GAGCCAAAGTGTACA[A/G]GGCTTTTACTGGGTA | 57097 |
rs73251502 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | PARP11 | GRCh38.p7 | 12:3865418 | TACTGTTGCTCATTT[C/T]CTATCTGCTCATTCC | 57097 |
rs73253304 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | PARP11 | GRCh38.p7 | 12:3866218 | CACGGTAACATTTCA[C/T]AGTTTATCCTCTGTC | 57097 |
rs73253309 | snp | C/T | 0.0260105 | 0.111035 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3872917 | GACAACAGTGCGAGA[C/T]TCCGTCTCAAAAACA | 57097 |
rs74056008 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PARP11 | GRCh38.p7 | 12:3842519 | GACAGCACGCTTGAC[A/G]GTTGTTGCCGAAGTA | 57097 |
rs74056009 | snp | A/C | 0.212122 | 0.247114 | intron-variant | PARP11 | GRCh38.p7 | 12:3858347 | ATGCAGAGAAAGTGG[A/C]TGTAGACAACATGAT | 57097 |
rs74056010 | snp | G/T | 0.212122 | 0.247114 | intron-variant | PARP11 | GRCh38.p7 | 12:3860563 | GCCTTAAGATTTCAT[G/T]GAACTTGCTCGGGAC | 57097 |
rs74056011 | snp | A/G | 0.212122 | 0.247114 | intron-variant | PARP11 | GRCh38.p7 | 12:3865289 | CATATATTTTTACAC[A/G]TTCTCTATGTAGTTG | 57097 |
rs74056012 | snp | A/T | 0.212425 | 0.24716 | intron-variant | PARP11 | GRCh38.p7 | 12:3866100 | CTTTCCTACCCATCA[A/T]CACTTAAAAACAAAC | 57097 |
rs74238893 | snp | A/G | 0.358515 | 0.225221 | intron-variant | PARP11 | GRCh38.p7 | 12:3849643 | TTGGTGGTTACCAGA[A/G]GCTGGGAAGGGCAGG | 57097 |
rs74474752 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PARP11 | GRCh38.p7 | 12:3859690 | TTTGAAATCCAGCTA[G/T]ATGCTGTCCACAGAA | 57097 |
rs74524532 | snp | A/C | 0 | 0 | intron-variant | PARP11 | GRCh38.p7 | 12:3822601 | GAGACTCCGTCTCAA[A/C]AAAAAAAAAAAAAAA | 57097 |
rs74703324 | snp | C/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PARP11 | GRCh38.p7 | 12:3811553 | TGATTTTCTCCTTCT[C/G]GCTTGTTTGACAGCA | 57097 |
rs74718532 | snp | A/G | | | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3874579 | TTTTAAAGTAGACTC[A/G]TGGCATTCCATAACT | 57097 |
rs74726727 | snp | A/G | 0.122411 | 0.214991 | intron-variant | PARP11 | GRCh38.p7 | 12:3847155 | CTAAGCAAACCAACA[A/G]TAAGTAACAAGATTG | 57097 |
rs74946880 | snp | C/T | | | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3870304 | ACAGTAGCAGTAAGA[C/T]AAATATGTCTTATTT | 57097 |
rs74996689 | snp | C/T | 0.122411 | 0.214991 | intron-variant | PARP11 | GRCh38.p7 | 12:3848008 | AATTAGTAGCATTTA[C/T]ACATGCCAAGAGCAA | 57097 |
rs75113467 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PARP11 | GRCh38.p7 | 12:3848945 | TATAAGGAGCTCAAA[C/G]AATTCAACAGCAAAA | 57097 |
rs75132987 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | PARP11 | GRCh38.p7 | 12:3863192 | CTGTATAGAGATACA[C/T]TGATTTTTGTATATG | 57097 |
rs75151877 | snp | A/G | | | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3870302 | ATACAGTAGCAGTAA[A/G]ACAAATATGTCTTAT | 57097 |
rs75203151 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | PARP11 | GRCh38.p7 | 12:3829774 | TTTTAGTTAAACAAT[C/T]TTATTTCCTTAAGCT | 57097 |
rs75412517 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PARP11 | GRCh38.p7 | 12:3818563 | TTAAATTTTAAAAAC[A/G]TAACATAACAATAAT | 57097 |
rs75433501 | snp | A/G | 0.5 | 0 | intron-variant | PARP11 | GRCh38.p7 | 12:3832262 | TACAATTCCTTATCA[A/G]ATTACACTATTTTTT | 57097 |
rs75486095 | snp | A/C | 0.5 | 0 | intron-variant | PARP11 | GRCh38.p7 | 12:3849702 | AATGGGTATAAATAT[A/C]CAGTTAGATATAAGA | 57097 |
rs75492151 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3837853 | TCCTGTAAAAAGAGA[C/T]AAAGAAGGTCAATAA | 57097 |
rs75569714 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | PARP11 | GRCh38.p7 | 12:3868523 | ACTTACCTCCCTAAC[C/T]AACTGCCTTCCAAAC | 57097 |
rs75607136 | snp | A/C | 0 | 0 | intron-variant | PARP11 | GRCh38.p7 | 12:3859561 | AGTGAGACTCTGCTA[A/C]AAAAAAAAAAAAAAA | 57097 |
rs75962260 | snp | G/T | | | utr-variant-5-prime, missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3829998 | TTTAGAAAATAATTC[G/T]TCTGCTTTGTGAAAC | 57097 |
rs75966484 | snp | A/G | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3811251 | TGTGCTGCAGAGGGG[A/G]AGGTAAAAAAAAATC | 57097 |
rs76011121 | snp | A/G | 0.0980852 | 0.198549 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3809386 | GTACATTCTCAGACC[A/G]AACAACAACAACAAG | 57097 |
rs76052031 | snp | A/G | 0.128288 | 0.218372 | intron-variant | PARP11 | GRCh38.p7 | 12:3849113 | AAACCACAATGAGAC[A/G]TCATCTCACCTCAGT | 57097 |
rs76063115 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3825851 | CCTGACTCAGCCTCC[C/T]GAGTAGCTGGGACCA | 57097 |
rs76114012 | snp | A/G | 0.100231 | 0.200173 | intron-variant | PARP11 | GRCh38.p7 | 12:3857784 | ACAACTGTTCTGCTC[A/G]TCCTCCAGCTGAAAT | 57097 |
rs76174774 | snp | A/C | | | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3870301 | AATACAGTAGCAGTA[A/C]GACAAATATGTCTTA | 57097 |
rs76199683 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PARP11 | GRCh38.p7 | 12:3836344 | AAACAAACAAAAAAA[A/G]AGCGCCTATCAACCA | 57097 |
rs76315635 | snp | C/T | 0.12932 | 0.218944 | intron-variant | PARP11 | GRCh38.p7 | 12:3821408 | AAATCCAGTAAGGAA[C/T]TGAGATTTTAAATCT | 57097 |
rs76401487 | snp | A/T | 0 | 0 | intron-variant | PARP11 | GRCh38.p7 | 12:3859562 | GTGAGACTCTGCTAA[A/T]AAAAAAAAAAAAAAA | 57097 |
rs76431733 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3848176 | CACCAAAAATGAAAA[A/G]ATATTCCACGTTCAT | 57097 |
rs76530375 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3811374 | ACACCTTGCACAGCA[A/G]GTCGTGGTGTAAGAA | 57097 |
rs76536944 | snp | C/G | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3811342 | TAATTTAAAGTTTCA[C/G]TTTGAAGATGCAATA | 57097 |
rs76847394 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3809556 | AGATAAGATCTGCAA[A/T]GTCTAAAAGAAAAAC | 57097 |
rs76964954 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | PARP11 | GRCh38.p7 | 12:3857588 | CAGGGAAAACCTCAC[A/G]TCCTCACTGTATTCA | 57097 |
rs76968637 | snp | A/C/T | 0.00279258 | 0.0372817 | intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3872293 | ATAAAAATAGAGATC[A/C/T]CCCTGGTCTCTGAAG | 57097 |
rs77027508 | snp | A/T | 0.5 | 0 | intron-variant | PARP11 | GRCh38.p7 | 12:3823931 | AAAAAAAAAAAAAAA[A/T]TGCTACAGGAACACA | 57097 |
rs77053633 | snp | G/T | 0.21875 | 0.248039 | intron-variant | PARP11 | GRCh38.p7 | 12:3835374 | TCAGCTATATCACTG[G/T]TATATACACATAAAC | 57097 |
rs77168957 | snp | A/T | 0.155656 | 0.231515 | intron-variant | PARP11 | GRCh38.p7 | 12:3812979 | AACTAATTTTTATAT[A/T]TTTTTAGTAGAGACA | 57097 |
rs77242556 | snp | A/T | | | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3870303 | TACAGTAGCAGTAAG[A/T]CAAATATGTCTTATT | 57097 |
rs77319296 | snp | C/T | 0.172028 | 0.23753 | intron-variant | PARP11 | GRCh38.p7 | 12:3825812 | GCTCACTTCAAGCTC[C/T]GCCTCACGGGTTCAC | 57097 |
rs77389892 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | PARP11 | GRCh38.p7 | 12:3823448 | AGATCTTTCTGTAAC[A/G]GTGCATAGAGAGCAT | 57097 |
rs77772728 | snp | C/G | 0.0998734 | 0.199905 | intron-variant | PARP11 | GRCh38.p7 | 12:3860029 | GAACGCAAGAAGAGA[C/G]AATGACTTAAAGACA | 57097 |
rs77828123 | snp | A/C/T | 3.47343e-05 | 0.00416725 | intron-variant | PARP11 | GRCh38.p7 | 12:3826126 | AAGAAAAAAAAAACC[A/C/T]ACTCTTTCCACCCCT | 57097 |
rs77836921 | in-del | -/A | | | intron-variant | PARP11 | GRCh38.p7 | 12:3836345 | ACAAACAAAAAAAAA[-/A]GCGCCTATCAACCAA | 57097 |
rs77935370 | snp | C/T | 0.5 | 0 | intron-variant | PARP11 | GRCh38.p7 | 12:3830659 | AACAATAATAGTAAC[C/T]TTTATATTACTTACT | 57097 |
rs78005342 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PARP11 | GRCh38.p7 | 12:3820839 | ATAGACCCAAGACTA[C/T]AAAGAACACAAGCTG | 57097 |
rs78065773 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PARP11 | GRCh38.p7 | 12:3850888 | AGAGAAGGACCAACT[A/G]TGAAAGTTCTATGTT | 57097 |
rs78175951 | snp | A/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3814791 | TTTCACAGAGAAATG[A/T]ATATAGTCATGTATT | 57097 |
rs78283810 | snp | A/C | 0.5 | 0 | intron-variant | PARP11 | GRCh38.p7 | 12:3835125 | GGCTAAATGCAGGAC[A/C]AAAAAAAATGTAAAC | 57097 |
rs78317981 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | PARP11 | GRCh38.p7 | 12:3866333 | GCACTTTGACTTCTC[C/G]TCAGCTTGTAACTTT | 57097 |
rs78406234 | snp | A/G | 0.0973687 | 0.197999 | intron-variant | PARP11 | GRCh38.p7 | 12:3833116 | TATAAATTTTAGTTT[A/G]CTACAACAAAGTATA | 57097 |
rs78686388 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3840744 | TTCATGGACATAGTT[A/G]GATAAAAGACCCGAA | 57097 |
rs78843406 | snp | C/G | 0.5 | 0 | intron-variant | PARP11 | GRCh38.p7 | 12:3863548 | ATTTCCTAGGACTCA[C/G]AAGACTCAAAAGTTG | 57097 |
rs78920040 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | PARP11 | GRCh38.p7 | 12:3868847 | TCTTTTGCTGCTAGA[A/G]CAAATTACCACAAAC | 57097 |
rs78952426 | snp | C/T | 0.0663309 | 0.169604 | intron-variant | PARP11 | GRCh38.p7 | 12:3833203 | ACTTCCTTGCCTCTA[C/T]ATATAAAGAAGATCT | 57097 |
rs79208366 | snp | C/G | 0.00716266 | 0.059414 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3811038 | AATGAAACAGCAAAA[C/G]AGATGGAACAGGTAA | 57097 |
rs79240529 | snp | A/T | 0.120674 | 0.21395 | intron-variant | PARP11 | GRCh38.p7 | 12:3814696 | TCTTCCCAAGGATAA[A/T]TCTATCCTAACACAT | 57097 |
rs79312542 | snp | G/T | 0.115438 | 0.210697 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3875184 | ATCCTTGGGAAGTTT[G/T]TTCCTAGATATTTTA | 57097 |
rs79362897 | in-del | -/AAAA | | | intron-variant | PARP11 | GRCh38.p7 | 12:3859574 | TAAAAAAAAAAAAAA[-/AAAA]GGCAGATGTAAATAA | 57097 |
rs79467007 | snp | A/G | 0.119281 | 0.213102 | intron-variant | PARP11 | GRCh38.p7 | 12:3860669 | TTTTTTAACTTTTTA[A/G]TTTTTTTAGAGACAG | 57097 |
rs79738974 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | PARP11 | GRCh38.p7 | 12:3835221 | CTACCTCAGGGAATG[A/T]AAGCACAACCTGTGA | 57097 |
rs79922552 | snp | A/T | 0.5 | 0 | intron-variant | PARP11 | GRCh38.p7 | 12:3846272 | AACTGTGTGCATATA[A/T]TTAAAAAAAAAAAGA | 57097 |
rs80129868 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3835607 | TTACAAATATGCTCA[A/C]AGACATAAATGAAAC | 57097 |
rs80162566 | snp | A/T | 0.39009 | 0.207062 | intron-variant | PARP11 | GRCh38.p7 | 12:3835379 | TATATCACTGTTATA[A/T]ACACATAAACCAATA | 57097 |
rs80164279 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3859859 | CTATAAAAAGTAGGG[C/T]CATTTTATCATGATA | 57097 |
rs80198699 | snp | C/T | 0.0154538 | 0.0865337 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3874997 | TATTTAATATATTTG[C/T]CTTTTCATAAAGGAA | 57097 |
rs80277165 | snp | A/G | 0.212728 | 0.247206 | intron-variant | PARP11 | GRCh38.p7 | 12:3862133 | ATTTTAAGATTTGAA[A/G]AAGATTTTTCTCAGC | 57097 |
rs80300179 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | PARP11 | GRCh38.p7 | 12:3829361 | TAAATCTTCTTTATA[C/T]AGTTTAGTAGAGTAA | 57097 |
rs80342408 | snp | A/C | 0.5 | 0 | intron-variant | PARP11 | GRCh38.p7 | 12:3828546 | CAGTGAGACGTCTCA[A/C]AAAAAAAAAAAAAAA | 57097 |
rs80345845 | snp | G/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3811144 | GGAGAAACCAGATTT[G/T]TCTCAAGCATCCCAT | 57097 |
rs80348850 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3859861 | ATAAAAAGTAGGGTC[A/C]TTTTATCATGATAAA | 57097 |
rs111230771 | snp | A/G | 0.174932 | 0.238463 | intron-variant | PARP11 | GRCh38.p7 | 12:3816999 | GATCCAGACCATCCT[A/G]GCTAACATGGTGAAA | 57097 |
rs111307959 | in-del | -/A | 0 | 0 | intron-variant | PARP11 | GRCh38.p7 | 12:3823916 | GTAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 57097 |
rs111344666 | snp | G/T | 0.5 | 0 | intron-variant | PARP11 | GRCh38.p7 | 12:3841317 | CAGTTGTCCTGTGTG[G/T]GCCCCACATTCTTAC | 57097 |
rs111412533 | snp | C/T | 0.5 | 0 | intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3872277 | TTCATGGGTCCTACG[C/T]ATAAAAATAGAGATC | 57097 |
rs111425759 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | PARP11 | GRCh38.p7 | 12:3825930 | AGACGGGGATTCACC[A/G]TGTGTTAGCCAAGAT | 57097 |
rs111623030 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | PARP11 | GRCh38.p7 | 12:3838984 | CTGGGTCCTGAGTCG[A/G]GCAGCGAGGCCGTCG | 57097 |
rs111808065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3815204 | AGAATCCCCTCCCCC[A/G]GCTTCTGATAGCTCT | 57097 |
rs111911675 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3840002 | ACGAGCAGCTGAAGA[A/G]CAATGGGAACTCTAC | 57097 |
rs111926319 | snp | C/T | 0.5 | 0 | intron-variant | PARP11 | GRCh38.p7 | 12:3846482 | AAAACTTGGATTGGG[C/T]GCAGTAGCTCATGCC | 57097 |
rs111981884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3832770 | TCGGTTATGAAGCAG[A/G]TATTTAATAATGTTA | 57097 |
rs112127353 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | PARP11 | GRCh38.p7 | 12:3822585 | GCCTGGGCGACAGGG[C/T]GAGACTCCGTCTCAA | 57097 |
rs112180459 | snp | C/T | | | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839284 | CCCTCGCGCCTGGCC[C/T]GCAGCAGGACCAGCA | 57097 |
rs112241817 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3871483 | AGGTTAAGAGCAATA[G/T]GCTATTCCATATAGC | 57097 |
rs112248088 | snp | A/C | 0.5 | 0 | intron-variant | PARP11 | GRCh38.p7 | 12:3827257 | CCTCTGAAACAGGAT[A/C]ATTACACAGAGGGTT | 57097 |
rs112403219 | snp | A/G | 0.5 | 0 | intron-variant | PARP11 | GRCh38.p7 | 12:3850248 | TAAAGTAATAATAAA[A/G]ATGTATAGTTGGGTT | 57097 |
rs112453775 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | PARP11 | GRCh38.p7 | 12:3817451 | GTTCTAGTGCCCACT[A/G]CTCCCACTACTAAGG | 57097 |
rs112567690 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3840138 | TGATTATTCCATTGC[C/T]GCTGGCTTACAATAT | 57097 |
rs112571745 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839923 | GATTCAGAGGATGAC[A/G]GCTGCAAGAGTAAAA | 57097 |
rs112786211 | in-del | -/A | 0.5 | 0 | intron-variant | PARP11 | GRCh38.p7 | 12:3827607 | TTGCCTAATGGCATT[-/A]AAAAAAAAAATGGCT | 57097 |
rs112912961 | snp | A/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3871419 | ATACTTTCCATTGTG[A/T]TACGAATGCCTACAG | 57097 |
rs112932403 | snp | A/C/T | 0.0279636 | 0.114961 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3840535 | CACAAAAATCTTAGC[A/C/T]GGACACCTTCACAGA | 57097 |
rs113042808 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3871541 | TACACTCTATGACGT[C/T]GGCACAATGAAAAAA | 57097 |
rs113045400 | snp | A/T | 0.5 | 0 | intron-variant | PARP11 | GRCh38.p7 | 12:3819583 | AACCACTGCTTTAAA[A/T]CCCTTCTCCACCACA | 57097 |
rs113045445 | snp | G/T | 0.5 | 0 | intron-variant | PARP11 | GRCh38.p7 | 12:3842617 | CCCAGTTGGAACTCT[G/T]TCCTCTCCCCAGCCT | 57097 |
rs113122277 | snp | C/T | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3873931 | ATGATTTATAGGTAA[C/T]ATGGTGAATAGAGAG | 57097 |
rs113127230 | snp | A/G | 0.5 | 0 | intron-variant | PARP11 | GRCh38.p7 | 12:3850817 | AATGTTAAGTCTGAA[A/G]TATCTTACAGAAGAG | 57097 |
rs113152224 | snp | C/T | 0.5 | 0 | intron-variant | PARP11 | GRCh38.p7 | 12:3813824 | CCCCACTATTCCTTA[C/T]TGCTCACTAATATTC | 57097 |
rs113254654 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | PARP11 | GRCh38.p7 | 12:3851476 | CGCACCTGGCTCAGC[A/G]GGTCCCATGCCCACA | 57097 |
rs113311349 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant, nc-transcript-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3871592 | TCAGAACATATCCCC[A/G]TTGTTAGGAGGCGCA | 57097 |
rs113376447 | snp | C/T | 0.5 | 0 | intron-variant | PARP11 | GRCh38.p7 | 12:3852738 | GGAGAACTTCCCCAA[C/T]CTAGCAAGGCAGGCC | 57097 |
rs113394255 | in-del | -/T | 0.5 | 0 | intron-variant | PARP11 | GRCh38.p7 | 12:3858925 | GAAACTCCATCTCTA[-/T]TTTAAAAAAAAAAAT | 57097 |
rs113462095 | snp | C/T | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3809149 | GTCTATTCATTCTCC[C/T]CACCCACTCTATGGG | 57097 |
rs113483947 | snp | A/G | 0.5 | 0 | intron-variant | PARP11 | GRCh38.p7 | 12:3837790 | GGAAAACAAAGAAGA[A/G]CAAAGAGTAGCTATA | 57097 |
rs113484743 | snp | C/T | 0 | 0 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3874878 | ACCTAAATTTGCATA[C/T]ACATATACATAGGTA | 57097 |
rs113540733 | snp | C/T | 0.5 | 0 | intron-variant, nc-transcript-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3871770 | TCTCTGAGGGTTGTG[C/T]TGGGGCTCAGAAAAT | 57097 |
rs113541971 | snp | G/T | 0 | 0 | intron-variant | PARP11 | GRCh38.p7 | 12:3866173 | CATTACTAAATCCTA[G/T]GCTCTTTTCAGTCCT | 57097 |
rs113625533 | in-del | -/CAA | 0.5 | 0 | intron-variant | PARP11 | GRCh38.p7 | 12:3838063 | TTCCAGCCAGAAAAT[-/CAA]CAACAACAACAACAA | 57097 |
rs113753290 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PARP11 | GRCh38.p7 | 12:3851884 | GACACCTCATACAGT[C/T]GGATGCCCCTCTGAG | 57097 |
rs113759022 | snp | A/T | 0.5 | 0 | intron-variant | PARP11 | GRCh38.p7 | 12:3867392 | GGAAAAAAGGTGCTG[A/T]CAAGTTTCTGAAATG | 57097 |
rs113761334 | snp | G/T | 0.5 | 0 | intron-variant | PARP11 | GRCh38.p7 | 12:3815752 | CCTCTCTTAGCTTGC[G/T]AAATCTGTGCAACTG | 57097 |
rs113943179 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | PARP11 | GRCh38.p7 | 12:3817146 | CAGTGAGCTGAGATC[A/G]CGCCACTGCACTCCA | 57097 |
rs113956251 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839996 | CAGGCAACGAGCAGC[C/T]GAAGAACAATGGGAA | 57097 |
rs113978157 | snp | C/T | 0.5 | 0 | intron-variant | PARP11 | GRCh38.p7 | 12:3857587 | ACAGGGAAAACCTCA[C/T]GTCCTCACTGTATTC | 57097 |
rs113987016 | snp | A/T | | | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3875133 | ATCTGCATCAGCATC[A/T]GTAAAAAAAAAAAAA | 57097 |
rs114109954 | snp | C/T | 0.100588 | 0.200439 | intron-variant | PARP11 | GRCh38.p7 | 12:3838911 | GCGCCTGGGGCGGGG[C/T]TTTTCTCGCTTCACA | 57097 |
rs114221419 | snp | A/T | 0.0475351 | 0.146656 | intron-variant | PARP11 | GRCh38.p7 | 12:3826963 | CATCATTCCATTTCA[A/T]AATGATTATGTTTAC | 57097 |
rs114291744 | snp | A/G | 0.0287284 | 0.116357 | downstream-variant-500B | PARP11 | GRCh38.p7 | 12:3808818 | GTGGAGATGAGATAC[A/G]TAAGTCACAGAAACA | 57097 |
rs114340419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3820878 | TTATTACCATAAACT[A/G]TTATGAGAATAAAAC | 57097 |
rs114360720 | snp | C/T | 0.129664 | 0.219133 | intron-variant | PARP11 | GRCh38.p7 | 12:3862594 | TATTTTATTAGTATA[C/T]TTTATATACTATATA | 57097 |
rs114440944 | snp | A/G | 0.00636936 | 0.0560724 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3874897 | TATACATAGGTATAC[A/G]TACACGTATATATCT | 57097 |
rs114457125 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | PARP11 | GRCh38.p7 | 12:3841319 | GTTGTCCTGTGTGGG[C/T]CCCACATTCTTACCT | 57097 |
rs114585688 | snp | C/G | 0.0115144 | 0.0749975 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3875332 | CTTGACAGCTCATCT[C/G]TATGAATTTGTACAC | 57097 |
rs114678419 | snp | A/T | 0.097727 | 0.198275 | intron-variant | PARP11 | GRCh38.p7 | 12:3812776 | AAACTGGTTTAATGA[A/T]TAAAAGTGTGGTTGG | 57097 |
rs114682842 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3830145 | CATGACACTTTAAAA[A/G]CAGCTTTCTATCTTT | 57097 |
rs114697630 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | PARP11 | GRCh38.p7 | 12:3834910 | ACCCACTGACAGAGC[A/G]GAGAAACTTCATTGG | 57097 |
rs114799780 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PARP11 | GRCh38.p7 | 12:3833030 | CTGTGTGGAAAATGA[A/G]TTTAAAGTCAAAATC | 57097 |
rs114846319 | snp | A/G | 0.0554779 | 0.157039 | intron-variant | PARP11 | GRCh38.p7 | 12:3851186 | TCCACAGCTCCCAGC[A/G]TGACTGACACAGAAG | 57097 |
rs114929727 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | PARP11 | GRCh38.p7 | 12:3829129 | CAGGGAATGGAGGGG[C/T]GAGGGAAACTTACTA | 57097 |
rs114940764 | snp | C/T | 0.244205 | 0.249933 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3840992 | CAACTTTTGGACCAA[C/T]AGGTGTCCCTGCTCC | 57097 |
rs114951031 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | PARP11 | GRCh38.p7 | 12:3827763 | CCTTCACTGTTTCTG[A/G]GCCTTGGTTCATCCA | 57097 |
rs114967909 | snp | C/T | 0.0279526 | 0.114869 | intron-variant, utr-variant-5-prime | PARP11, LOC105369609 | GRCh38.p7 | 12:3872435 | TACTAAAGTTTTCGG[C/T]CCCTACGTTGCACTT | 57097 |
rs115140685 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | PARP11 | GRCh38.p7 | 12:3827012 | GTATAAAGTGTGTTC[C/T]GTCCTTTCTGTGTTC | 57097 |
rs115202040 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | PARP11 | GRCh38.p7 | 12:3832123 | CCTTACCTAAGACTT[C/T]GCTTTAGGCCAGGTT | 57097 |
rs115327950 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | PARP11 | GRCh38.p7 | 12:3841901 | CAGTTTCCACAGTAG[A/G]TGAGTTTCCAGCAGC | 57097 |
rs115996303 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PARP11 | GRCh38.p7 | 12:3837837 | ATAGACTATGAACAA[A/G]TCCTGTAAAAAGAGA | 57097 |
rs115998034 | snp | A/G | 0.039522 | 0.134904 | intron-variant | PARP11 | GRCh38.p7 | 12:3867534 | AGAATTTTAAATAGC[A/G]TGAACCTACTACTTC | 57097 |
rs116520483 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | PARP11 | GRCh38.p7 | 12:3865061 | CACCATCCTACAAAT[C/T]TGATATGTTGTTTTC | 57097 |
rs116541710 | snp | A/G | 0.0126979 | 0.078662 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3875377 | ACCTGCAAATAATGC[A/G]TTTCTTTCTTCCTAT | 57097 |
rs116668113 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3811421 | GATGAAGTGTAGGCT[A/G]ATGACATTTTGCAGC | 57097 |
rs116705093 | snp | C/T | 0.0263992 | 0.111815 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3840165 | ATATGAAGTTGGAGA[C/T]AAATGTCAAGTTAGG | 57097 |
rs116739637 | snp | A/T | 0.00755907 | 0.0610114 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3874602 | CCATAACTTATGCGT[A/T]TACTACGTACACACA | 57097 |
rs116788805 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | PARP11 | GRCh38.p7 | 12:3859595 | CAGATGTAAATAATA[A/G]TATAACATGCAATTA | 57097 |
rs116866214 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | PARP11 | GRCh38.p7 | 12:3829550 | ATCAATGTACAACAC[A/C]TAACATAATACCTGG | 57097 |
rs116866812 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3835609 | ACAAATATGCTCAAA[A/G]ACATAAATGAAACTT | 57097 |
rs116883954 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PARP11 | GRCh38.p7 | 12:3850808 | CTGGACAGCAATGTT[A/G]AGTCTGAAATATCTT | 57097 |
rs116896238 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3870381 | TTTTAACAAAAGTCA[C/G]CCTGCTCTGCTGAAA | 57097 |
rs116988326 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | PARP11 | GRCh38.p7 | 12:3837526 | AGAAAGGAAGATGTA[A/C]GAAAGGAAGAGAGCA | 57097 |
rs117103552 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | PARP11 | GRCh38.p7 | 12:3832731 | GACACATTTATAGGT[A/G]ATAAAAAGAATATTC | 57097 |
rs117120452 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3846968 | TGTGGTCCCAAATAC[C/T]TGGGAGGCTGAGGTG | 57097 |
rs117309640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3830276 | CAACCATTTAAGTAA[A/G]CTATATCAACATCAA | 57097 |
rs117547847 | snp | C/T | 0.0103295 | 0.0711199 | downstream-variant-500B | PARP11 | GRCh38.p7 | 12:3808405 | GCCTTTGATACCATC[C/T]TTTCTTGCCAAAGGT | 57097 |
rs117716956 | snp | A/T | 0.0146672 | 0.084371 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3872691 | AGACAAGGGGGTCCC[A/T]ATTCCCTTGCTTTAG | 57097 |
rs117755625 | snp | A/C | 0.128976 | 0.218754 | intron-variant | PARP11 | GRCh38.p7 | 12:3846663 | TCGGGAGGCTGAATC[A/C]GGAAAATGGCGTGAA | 57097 |
rs117781650 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | PARP11 | GRCh38.p7 | 12:3838462 | AAGCAGTACTAAAAG[A/T]GAAGTTTATAGCAAT | 57097 |
rs117890926 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | PARP11 | GRCh38.p7 | 12:3849701 | TAATGGGTATAAATA[C/T]ACAGTTAGATATAAG | 57097 |
rs117911054 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | PARP11 | GRCh38.p7 | 12:3836735 | GCCAGCAATATCCCA[C/G]AATGCAAATATTATG | 57097 |
rs118014543 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3809750 | CTAATGTCTCTAACA[C/T]TGTTTTTTGTGAACG | 57097 |
rs118120762 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PARP11 | GRCh38.p7 | 12:3845636 | TAGCTGAAGAGAATA[C/T]GTATTTGGCTACACT | 57097 |
rs118129412 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PARP11 | GRCh38.p7 | 12:3828630 | ATAAAACAACTGATA[C/T]GGTGTTTTGTGTTCC | 57097 |
rs137886893 | snp | A/G | 1.64757e-05 | 0.00287012 | intron-variant, missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3828990 | TTGAAGCTTTTTTCG[A/G]TATCTTCACTGCTAA | 57097 |
rs137909637 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | PARP11 | GRCh38.p7 | 12:3846573 | CATCCTGGCTAACAC[A/G]GTGAAACCCCGTCTC | 57097 |
rs137953102 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3820223 | TTTTTGTTAGAAGAA[A/G]TGGGGAAAGTAAGAG | 57097 |
rs137962694 | in-del | -/GAG | 0.039522 | 0.134904 | intron-variant | PARP11 | GRCh38.p7 | 12:3812582 | TCTGCAGATCTTTAA[-/GAG]AAGAATAGAAATCCA | 57097 |
rs137987208 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PARP11 | GRCh38.p7 | 12:3855083 | AACAAAATTCAACAA[C/T]GCTTCATGCTAAAAA | 57097 |
rs138026951 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3852303 | GACGAGTTGACAGAA[A/G]TTGGCTTCAGAAGGT | 57097 |
rs138055592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3826868 | TCATACCAATATTTA[C/T]CAGGTCCATTTCTTC | 57097 |
rs138064935 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | PARP11 | GRCh38.p7 | 12:3851341 | CAAGGGATTGGGGGA[G/T]TTCCCTTTCCTAGCC | 57097 |
rs138076334 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PARP11 | GRCh38.p7 | 12:3858671 | TGCCACTGTTTGCTG[C/T]TGCTGTTGTTTAACA | 57097 |
rs138138652 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | PARP11 | GRCh38.p7 | 12:3836246 | ATAAGAGAATCCTAA[C/T]GAGATTAACAGCTGA | 57097 |
rs138202847 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PARP11 | GRCh38.p7 | 12:3862161 | AGCCAGGCATAGTGG[C/T]TCATCCCTGTAATCA | 57097 |
rs138267045 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3833255 | AAAAATGAACGAGAA[C/G]TTCCAGAATGACAGA | 57097 |
rs138367999 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PARP11 | GRCh38.p7 | 12:3842995 | TGCCTTAGTCATAAA[C/T]TGGGCTCAGACAATT | 57097 |
rs138402085 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | PARP11 | GRCh38.p7 | 12:3841533 | GCCAGTGATTGGACC[A/G]CCGACATTTTCTTCA | 57097 |
rs138485510 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PARP11 | GRCh38.p7 | 12:3813314 | TAGAATCCCATATCC[A/G]TGAAAAGATTTCTGA | 57097 |
rs138509100 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3871954 | CCAGAATTCTTCCCC[A/T]AGGTGAGTGATAGAA | 57097 |
rs138530843 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | PARP11 | GRCh38.p7 | 12:3868626 | GGCTCAGTGAAAACA[C/T]CTTATTCCTGGCTGC | 57097 |
rs138547609 | snp | C/T | 0.0154538 | 0.0865337 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810514 | AGAATTGCTTGAACC[C/T]GGGAGGTGGAGGTTG | 57097 |
rs138696419 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3822001 | ATTGTGCAGAGGAAT[A/G]AGCTGGAAAAATAAA | 57097 |
rs138698498 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3809557 | ATAAGATCTGCAAAG[-/T]TCTAAAAGAAAAACA | 57097 |
rs138730941 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3821754 | TGAGACCAGGTCAAA[A/C]TACGGCAAGAGAAAA | 57097 |
rs138747319 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | PARP11 | GRCh38.p7 | 12:3833028 | AGCTGTGTGGAAAAT[G/T]AGTTTAAAGTCAAAA | 57097 |
rs138780704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3836810 | TGAGCAGACAGTAAC[A/G]GAATTGGATTTCCTC | 57097 |
rs139000351 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810012 | ATTACACATATGCTG[A/G]TCTATAACGGAAATC | 57097 |
rs139021786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3849772 | TCAGTAGGGTGACTG[C/T]AGTTTACAATAATCT | 57097 |
rs139088320 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PARP11 | GRCh38.p7 | 12:3864715 | TTCATAACATTCCTT[C/T]ATTATCCTTTTAATG | 57097 |
rs139160388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3868168 | AATTTCTAAAATACT[A/G]TTTTATTGGGGGCCA | 57097 |
rs139206981 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PARP11 | GRCh38.p7 | 12:3817224 | TTATCACTACTTTTC[A/G]GGCACAAATTCGATT | 57097 |
rs139211723 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3844275 | GGATGGTTGTGTGGA[A/C]AACATTTTTTGAGAG | 57097 |
rs139229671 | snp | C/G | 0.122064 | 0.214785 | intron-variant | PARP11 | GRCh38.p7 | 12:3853720 | TGTCAATATTAGATA[C/G]ATCAACGAGACAGAA | 57097 |
rs139252105 | in-del | -/GAG | 0.240478 | 0.249819 | intron-variant | PARP11 | GRCh38.p7 | 12:3834791 | CCCTCTTAGATCAGA[-/GAG]GAGTCAGAAAGGCAG | 57097 |
rs139337483 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PARP11 | GRCh38.p7 | 12:3856695 | AAACTAGTTCAACCA[C/T]TGTGGAAGATGGAAG | 57097 |
rs139406418 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3870723 | AAACCCCTGTCCTTG[C/T]GGATCTTACAATATA | 57097 |
rs139511608 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839930 | AGGATGACAGCTGCA[A/G]GAGTAAAACTGCTGT | 57097 |
rs139585014 | in-del | -/AAAG | | | intron-variant | PARP11 | GRCh38.p7 | 12:3846780 | AAAAAAGAAAAGAAA[-/AAAG]AAAGAAATAGAAAAC | 57097 |
rs139605577 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PARP11 | GRCh38.p7 | 12:3828087 | AGATTATCTGGCTAA[C/T]CTGTGGAAGAGCCAA | 57097 |
rs139636840 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | PARP11 | GRCh38.p7 | 12:3823860 | GGCGGAGGCTGCAGT[A/G]AGCCAAGATGGCACC | 57097 |
rs139643894 | in-del | -/GAAGAG | | | cds-indel, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810783 | AAGAGGAGAGGAAGA[-/GAAGAG]GAAGAGGAAGACAGA | 57097 |
rs139648380 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3874506 | CCAGGTGATCCACCT[A/G]CCTTGGCCTCCCAAA | 57097 |
rs139758125 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | PARP11 | GRCh38.p7 | 12:3847183 | TTGAAGCTGTAATTA[C/T]GTCTCCCATCAAAGA | 57097 |
rs139836173 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PARP11 | GRCh38.p7 | 12:3829308 | ATTACAATTTTTACA[C/G]ATTATTCCAATAATT | 57097 |
rs139859426 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3872943 | AAACAACAACAACAA[A/C]AAATGGTGAAGGGAT | 57097 |
rs139879842 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3870143 | AAGTGAAATTGTGGT[A/G]AGTGAAACCAGGAAA | 57097 |
rs140053851 | in-del | -/CAC | 0.390838 | 0.206555 | intron-variant | PARP11 | GRCh38.p7 | 12:3845047 | GAAATTATGAAACTT[-/CAC]CATATTATGATCATA | 57097 |
rs140056588 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PARP11 | GRCh38.p7 | 12:3854613 | TCCCTGAATAGACCA[C/G]TAACAGGATCTGAAA | 57097 |
rs140068882 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3856229 | GCAAGGACTTCATGA[A/C/T]TAAAACACCAAAAGC | 57097 |
rs140088951 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3853981 | TCAGGATTAAGAAAC[G/T]CACTCAAAACCACAC | 57097 |
rs140132565 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3838159 | TGGAGAATACACATT[A/C]TTTTCATCAACACAT | 57097 |
rs140172629 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3834810 | AGTCAGAAAGGCAGT[A/G]TAAAAACACTAGGCT | 57097 |
rs140210586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3831214 | TTCTCCAGGGTTAGC[C/T]AATGCTATAATTTCA | 57097 |
rs140216006 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3863249 | ACTCATTTATTAGTT[C/G]TAAGAGCTTTTTAAA | 57097 |
rs140256101 | in-del | -/CGTGC | 0.119978 | 0.213528 | intron-variant | PARP11 | GRCh38.p7 | 12:3812948 | CTGGGATTACAGGCG[-/CGTGC]CGTGCCACCACACCC | 57097 |
rs140258763 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3860278 | GACTTCTTGGATTTT[G/T]CAGGATGGGACCATA | 57097 |
rs140264149 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3857977 | TTTTCAAAAGTAGTT[G/T]AGCATGGAGGATGCC | 57097 |
rs140320904 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3840068 | TCAATCCTGCAGTCT[A/G]TAGAAATGTGGAATA | 57097 |
rs140345403 | in-del | -/TAAC | | | intron-variant | PARP11 | GRCh38.p7 | 12:3848101 | ACATACGAGTCAATT[-/TAAC]TAAAATGAAAGATCT | 57097 |
rs140403108 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3835973 | GAAAAAGGCACAGGA[A/G]AAACTTTAAAGAAAG | 57097 |
rs140438512 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PARP11 | GRCh38.p7 | 12:3865876 | TAGCTTTAAGTTTAC[A/G]TCTTGTTATTTGCTT | 57097 |
rs140480988 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3861886 | AAAAATTAGCCAGGC[A/G]TGGTGGAGGGTGCCT | 57097 |
rs140495946 | snp | G/T | 0.0174175 | 0.0916809 | intron-variant | PARP11 | GRCh38.p7 | 12:3841410 | TGTTTATCTTCATAA[G/T]CCCTGGTTCAAAGAG | 57097 |
rs140511398 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PARP11 | GRCh38.p7 | 12:3848538 | TCAACAAAGTCACCA[C/T]GAACATAGAATGGGA | 57097 |
rs140596160 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810947 | CTATGCAACATGCCC[A/G]CCAAGTTGCTGTCTC | 57097 |
rs140631178 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PARP11 | GRCh38.p7 | 12:3851885 | ACACCTCATACAGTC[A/G]GATGCCCCTCTGAGA | 57097 |
rs140670600 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PARP11 | GRCh38.p7 | 12:3848087 | AAAGAATATAAAATA[C/T]ATACGAGTCAATTTA | 57097 |
rs140711762 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | PARP11 | GRCh38.p7 | 12:3812976 | CCCAACTAATTTTTA[C/T]ATTTTTTTAGTAGAG | 57097 |
rs140798162 | in-del | -/A | 0.227369 | 0.248974 | intron-variant | PARP11 | GRCh38.p7 | 12:3836336 | AAGTAAAAAACAAAC[-/A]AAAAAAAAAGCGCCT | 57097 |
rs140936299 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PARP11 | GRCh38.p7 | 12:3867334 | GAAGGAAATGGCAGC[A/G]TTTGCAAGATTATTC | 57097 |
rs140971886 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | PARP11 | GRCh38.p7 | 12:3865239 | CTTCAATTCTTTCAA[A/T]TGTACTGAGATATGT | 57097 |
rs141036909 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3838918 | GGGCGGGGCTTTTCT[A/C]GCTTCACACCGGTAC | 57097 |
rs141110879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3861236 | ATGTTATAGACTAAA[C/T]GTTTGTGTCCTTGCC | 57097 |
rs141113424 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PARP11 | GRCh38.p7 | 12:3819736 | CGTGGTCTAGCCCCC[G/T]CTAACTCTCTGACTT | 57097 |
rs141144974 | in-del | -/TC | 0.0437281 | 0.141251 | intron-variant | PARP11 | GRCh38.p7 | 12:3831245 | TGCATATCTTTCAGA[-/TC]TCTCTCTCTCTCTCT | 57097 |
rs141225422 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PARP11 | GRCh38.p7 | 12:3851257 | TGTCATTGGGACTGG[C/T]TGGGCAGCGGGTGCA | 57097 |
rs141256699 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3826292 | TGTACTATAAAGTGT[C/T]ATGAAGATTAATAGC | 57097 |
rs141329536 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PARP11 | GRCh38.p7 | 12:3851686 | TCTGGGGGCAGGGCA[C/T]AGCTGAACAAAAGGC | 57097 |
rs141384660 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3853415 | CAGAGACACACACAG[A/G]CTCCAAATAAAGGGA | 57097 |
rs141388668 | in-del | -/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3825110 | TACCTTTTTTTTTTT[-/T]CCAGTTTCATTTTAA | 57097 |
rs141426865 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | PARP11 | GRCh38.p7 | 12:3848718 | TACTAGAAGAAAACA[C/T]TGGGGAAATAAGAAC | 57097 |
rs141497323 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PARP11 | GRCh38.p7 | 12:3843422 | AGAAGAAATGTTAAA[A/G]ATTTTTAGCTTGACA | 57097 |
rs141594640 | in-del | -/T | 0.131381 | 0.220067 | intron-variant | PARP11 | GRCh38.p7 | 12:3822732 | TGTCTTGTTTTTTTT[-/T]GAAATTTCCAAAATT | 57097 |
rs141683889 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant, nc-transcript-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3871721 | CAGTTTCAACCATAA[C/T]AACAGAAGAATACTC | 57097 |
rs141687128 | snp | C/T | 0.00874735 | 0.0655527 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3873597 | GTGATCTTAAAGCCA[C/T]GGCTGGCTGTATTTC | 57097 |
rs141701204 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3816296 | CAACAAATAAGCTAC[C/T]CCTTCTAGTTTTGAA | 57097 |
rs141823746 | snp | C/G | 0.0279526 | 0.114869 | intron-variant | PARP11 | GRCh38.p7 | 12:3836318 | ATCATTCTCAAAATA[C/G]ATAAAGTAAAAAACA | 57097 |
rs141888948 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | PARP11 | GRCh38.p7 | 12:3833052 | GTCAAAATCCTGGTC[C/T]ATATAAGGAAAATAA | 57097 |
rs141918096 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3824855 | TATTATTTGTACTAA[A/G]GAATGTGGATATGAC | 57097 |
rs141928332 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3827713 | ATAATAATTATTGCA[A/T]ATTTGGTTCCATCAA | 57097 |
rs141933321 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3859304 | GTGCAGTGGCTCACG[A/T]CTGTAATCCTAGCAC | 57097 |
rs141947117 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3872090 | TGCCTGATAGTAGGT[C/T]GCTAAGACCCTCATT | 57097 |
rs142058488 | snp | C/G | 0.0217236 | 0.101931 | intron-variant | PARP11 | GRCh38.p7 | 12:3857133 | GGCCTGTCGGGGGGT[C/G]GGGGGCTGGGGGAAG | 57097 |
rs142082066 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PARP11 | GRCh38.p7 | 12:3856399 | AATATCCAGAATCTA[C/T]AAAGAACTCAAACAA | 57097 |
rs142098492 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | PARP11 | GRCh38.p7 | 12:3855357 | TGTCCCTGTTTGCAG[A/T]TGACATGATTGTACA | 57097 |
rs142135252 | snp | A/C/T | 6.59776e-05 | 0.00574326 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3821978 | ACTTCATTATATTCA[A/C/T]GTGTTTGATTGTGCA | 57097 |
rs142272418 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810080 | CTGTCTGCACTCTTT[A/G]CTTTTATTATTTGTA | 57097 |
rs142279619 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | PARP11 | GRCh38.p7 | 12:3848302 | CAGAAATAAACAAAC[A/G]CAAAAAATCCTAAAA | 57097 |
rs142317597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3850527 | TCACATGTCCAGATT[C/T]CCCCACGCAAGCATG | 57097 |
rs142470434 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | PARP11 | GRCh38.p7 | 12:3843034 | AAAACACTGTTGTCT[G/T]TTAAAATGCTTCCAA | 57097 |
rs142483542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3824605 | CCTCTCCTTTTATTA[C/T]TATCTTGCTTATTGT | 57097 |
rs142499296 | snp | C/T | 0.41275 | 0.189769 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839116 | GCATTAGGCAGGGCT[C/T]CCCTACGCGCCCGGA | 57097 |
rs142518506 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3869751 | TATCTTTTTATCACA[A/T]TTTAAATTAAATGTA | 57097 |
rs142609402 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | PARP11 | GRCh38.p7 | 12:3860773 | CCTCGAACTCCTAGT[A/G]TCAAGTGATCCTTGT | 57097 |
rs142697520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3858707 | TAAAGGTATTTTGGT[A/G]ATGCTATTGCACTGC | 57097 |
rs142750141 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant, missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3828920 | CATACCTGCAAAGTC[C/T]ATCTTGTAGCTGAAT | 57097 |
rs142769901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3833938 | CTCTCCTTCAGCCCA[A/G]AGGTGTAGAAGCTCT | 57097 |
rs142785395 | snp | C/T | 1.65411e-05 | 0.00287581 | synonymous-codon, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3821884 | TCACCTGCAAAAGAA[C/T]TCCCACAAATCTAGG | 57097 |
rs142803197 | snp | C/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3811285 | GAAGTGATCATTGTA[C/G]GGACTCTTTTTAAAA | 57097 |
rs142910026 | snp | A/C | 0.000165462 | 0.00909414 | utr-variant-5-prime, stop-gained, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3829997 | TTTTAGAAAATAATT[A/C]TTCTGCTTTGTGAAA | 57097 |
rs142950512 | snp | C/T | 0.122411 | 0.214991 | intron-variant | PARP11 | GRCh38.p7 | 12:3854374 | AAAAGATCAACAAAA[C/T]TGATAGACCGCTAGC | 57097 |
rs143039336 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3850606 | GGCAGGTTCCTCACA[A/G]TGCCCCACAAGAGGC | 57097 |
rs143123996 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | PARP11 | GRCh38.p7 | 12:3835284 | CACATAAGTAGTCAG[A/G]TTAAGAGGGGAAAAG | 57097 |
rs143179331 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | PARP11 | GRCh38.p7 | 12:3842291 | GAAGTGGTAGATCCA[A/T]GCAGTTCTATAATCA | 57097 |
rs143183768 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | PARP11 | GRCh38.p7 | 12:3868199 | GGCACGGTGGTTCAC[A/G]ACTGTAATCCCACCA | 57097 |
rs143223892 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PARP11 | GRCh38.p7 | 12:3862804 | CCTAACTTGATGCCA[A/G]TACTACACTGTTTTG | 57097 |
rs143261427 | in-del | -/TT | 0.097727 | 0.198275 | intron-variant | PARP11 | GRCh38.p7 | 12:3850761 | GCATTTATATTTATC[-/TT]TACAAAACAGAAAGT | 57097 |
rs143349246 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3809966 | TATTGTACATGCAAT[A/G]TCCTGGGTACTACTT | 57097 |
rs143399365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3865288 | GCATATATTTTTACA[C/T]GTTCTCTATGTAGTT | 57097 |
rs143457451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3815855 | TAACAGTAAAATATC[C/T]GTATCTCAGACTGAG | 57097 |
rs143476201 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PARP11 | GRCh38.p7 | 12:3852196 | ACCAGAGCAGAAAAG[C/T]TGAAAATTCTAAAAA | 57097 |
rs143522159 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PARP11 | GRCh38.p7 | 12:3831573 | AATGTTATAAATGAA[C/T]GAGACAAGTTCATTT | 57097 |
rs143591330 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | PARP11 | GRCh38.p7 | 12:3823424 | GGTTTTTACTTCATA[A/G]CTTCTTAGAGATCTT | 57097 |
rs143597749 | snp | A/G | 0.212425 | 0.24716 | intron-variant | PARP11 | GRCh38.p7 | 12:3852402 | GAAAAAAGATTAGAC[A/G]AATGGCTAACTAGAA | 57097 |
rs143636841 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PARP11 | GRCh38.p7 | 12:3851366 | CTAGCCAAGGGAAGC[C/T]GTGACAGATTGTACC | 57097 |
rs143650196 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PARP11 | GRCh38.p7 | 12:3866313 | ATAAATTCTCAGTCT[C/T]CTTTGCACTTTGACT | 57097 |
rs143738965 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | PARP11 | GRCh38.p7 | 12:3818142 | AGCTAAGCCCTCAAC[G/T]CTGACAGAAATCCTG | 57097 |
rs143774491 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PARP11 | GRCh38.p7 | 12:3845648 | ATACGTATTTGGCTA[C/T]ACTATTTCTGTGTAC | 57097 |
rs143777975 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | PARP11 | GRCh38.p7 | 12:3854027 | GAACAATCTGCTCCT[A/G]AATGACTACTAGGTA | 57097 |
rs143815152 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3851731 | CAGACTTAAATGTCC[A/G]TGTCTGACAGCTCAG | 57097 |
rs143871848 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3842112 | GTGCCTGTTGAACTT[C/G]AACCTAAAAGGACCA | 57097 |
rs143956426 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | PARP11 | GRCh38.p7 | 12:3841688 | AGAATATGTTCCCCC[A/G]GCCATCTTTTGGACC | 57097 |
rs143994377 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3838414 | CAAATGAAAGTGGAG[A/C]TACAAAATACCAAAA | 57097 |
rs144093579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3827251 | TCCATGCCTCTGAAA[C/T]AGGATCATTACACAG | 57097 |
rs144176377 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3831231 | ATGCTATAATTTCAC[G/T]GCATATCTTTCAGAT | 57097 |
rs144180274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3864083 | TAACCCCCTTCCACA[C/T]ACCGTCCATCAGGTT | 57097 |
rs144217958 | in-del | -/TA | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3840613 | AGTCGAGAATCTAAC[-/TA]TTGCTACTTCTCAGA | 57097 |
rs144220523 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | PARP11 | GRCh38.p7 | 12:3860364 | GCAATTCAGAGATCA[G/T]CCGGGATGCTTCCTT | 57097 |
rs144339428 | snp | A/G | 0.416055 | 0.186885 | intron-variant | PARP11 | GRCh38.p7 | 12:3828497 | AGGCTGCAGTGAGCC[A/G]AGATCATGCCACTGC | 57097 |
rs144381061 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PARP11 | GRCh38.p7 | 12:3824178 | TTTTAGTCAATCTGG[C/T]AGTAAAAATTAGTCT | 57097 |
rs144418385 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PARP11 | GRCh38.p7 | 12:3819201 | TCACTCCATCGCATA[C/T]AATAAGTGAGGCGCC | 57097 |
rs144422778 | in-del | -/A | | | intron-variant | PARP11 | GRCh38.p7 | 12:3848972 | AAAAGAAAAAAAAAA[-/A]CACAAATAATCCAAT | 57097 |
rs144440773 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3869697 | TGCCCAGTCTAGTAT[C/T]AGCTCCCCCTACACT | 57097 |
rs144563139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3847056 | CACTCCAGCCTGGTC[A/G]ACAGAGAGAGATCCT | 57097 |
rs144584425 | in-del | -/AG | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810735 | GAAAGAGAAAGAGAA[-/AG]AGGAAGAGAAAAAGG | 57097 |
rs144695454 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PARP11 | GRCh38.p7 | 12:3851571 | GAGGGGTTTCCACCA[C/T]TGCTGAGGCTTGAGT | 57097 |
rs144824076 | snp | C/G/T | 0.000115333 | 0.00759303 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3829950 | CCACTGGGTATCTGA[C/G/T]GTGTCCATGTCATCC | 57097 |
rs144840918 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | PARP11 | GRCh38.p7 | 12:3861494 | TGCAGTGTCTATTCA[C/T]ATCTTTAGCTCACTT | 57097 |
rs144932714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3835250 | GACCAGTACATAGTC[C/T]ATGCCAATCCAGAAA | 57097 |
rs144951646 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | PARP11 | GRCh38.p7 | 12:3864865 | TAGCTTTCAGTATCA[C/T]TGATCTTCACTGTTG | 57097 |
rs144970299 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PARP11 | GRCh38.p7 | 12:3859763 | GGATAAATAAAAAAT[A/G]CCATGCAAACAACAG | 57097 |
rs144977708 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | PARP11 | GRCh38.p7 | 12:3858818 | ATTCAGGCTGGGTGC[A/G]GTGGCTCACGCCTGT | 57097 |
rs145009384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3856886 | ACCAACCCAAATGTC[C/T]ATCAATGATAGACTG | 57097 |
rs145096701 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812021 | TTCATATCTGTTTCA[A/G]AAGTATCAGATAATT | 57097 |
rs145098273 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3871351 | TATACAAGTGGTCCC[A/G]AAGATTGTTAACACT | 57097 |
rs145138411 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | PARP11 | GRCh38.p7 | 12:3848970 | GCAAAAGAAAAAAAA[A/C]AACACAAATAATCCA | 57097 |
rs145209460 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PARP11 | GRCh38.p7 | 12:3817837 | CATCAGAGCCACTTA[C/T]GGAATTTTTTAAGGT | 57097 |
rs145232231 | in-del | -/T | 0.0275645 | 0.114116 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3809586 | AACTCCCAAATGCTG[-/T]TAACAGTTTTTCCAT | 57097 |
rs145234099 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | PARP11 | GRCh38.p7 | 12:3846320 | AATAAAATCAGAAAT[G/T]AAAAAGGTGACAACT | 57097 |
rs145247853 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3809855 | TCTAGATGCTTTTTA[A/G]AGCGCTTTTTCTAAA | 57097 |
rs145321387 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PARP11 | GRCh38.p7 | 12:3847270 | ATGCTAATTCTACTT[A/C]AACTCTTCAAAAAAA | 57097 |
rs145372104 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3824392 | AAACACACTTGGCCT[A/G]AAGTATCTTTTAGCT | 57097 |
rs145376500 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | PARP11 | GRCh38.p7 | 12:3848661 | AAAAAATCAAATCAA[A/G]ATGAATTAAAGACTT | 57097 |
rs145499071 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PARP11 | GRCh38.p7 | 12:3860523 | CTCTGGAAGGCAGAG[C/T]ATCAAGCCAATCATT | 57097 |
rs145513104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3836179 | AAAATTTCGAAAGCC[A/G]AAGACAAACAGAAAA | 57097 |
rs145513818 | in-del | -/T | 0.0260105 | 0.111035 | intron-variant | PARP11 | GRCh38.p7 | 12:3846069 | AAGTATATATACGTA[-/T]CTTTTGAAGTGTTAA | 57097 |
rs145576712 | in-del | -/G | 0.0414363 | 0.137845 | intron-variant | PARP11 | GRCh38.p7 | 12:3836538 | ATGGGGGATAAAAAA[-/G]AAAAGAGCGCTGGTA | 57097 |
rs145634539 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3833159 | AGCATGAGTATAGTA[A/T]CTTCAGGAAATCATA | 57097 |
rs145703985 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | PARP11 | GRCh38.p7 | 12:3834836 | AGGCTGTGTACACCC[A/T]GGAATGATCAGGGCA | 57097 |
rs145781826 | snp | G/T | 0.00716266 | 0.059414 | | | GRCh38.p7 | 12:3825074 | AAATCTCCTTGGAAG[G/T]AGCAAATAGGCATTC | 57097 |
rs145824809 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | PARP11 | GRCh38.p7 | 12:3857288 | TAATAATAATAATAA[A/T]AAAAAGATACAGCAT | 57097 |
rs145879477 | snp | C/T | 1.64939e-05 | 0.0028717 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3821987 | TATTCATGTGTTTGA[C/T]TGTGCAGAGGAATAA | 57097 |
rs145927609 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | PARP11 | GRCh38.p7 | 12:3855470 | GTGCAAAAATCACAA[A/G]CATTCCTACACACCA | 57097 |
rs145949649 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3872776 | GCCAGTTACTCCAAT[C/T]AGAAAGCAAAACACA | 57097 |
rs146068966 | snp | A/C | 0.0966517 | 0.197444 | intron-variant | PARP11 | GRCh38.p7 | 12:3856135 | TTTTCAAGATGGATT[A/C]AAGACTTAAATGTTA | 57097 |
rs146114938 | in-del | -/A | | | intron-variant | PARP11 | GRCh38.p7 | 12:3849265 | GGTACCTCAAAAAAA[-/A]AATAGAACTACCATA | 57097 |
rs146213136 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3873689 | CAATGGCATTTGGGA[A/G]AAACTTCATAATCTT | 57097 |
rs146311305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3827886 | AGCTAAAGGACCAAG[C/T]TGTGTAGCAAACAAA | 57097 |
rs146335537 | in-del | -/AAAG | 0.489722 | 0.0709447 | intron-variant | PARP11 | GRCh38.p7 | 12:3846779 | AAAAAAAGAAAAGAA[-/AAAG]AAAAGAAATAGAAAA | 57097 |
rs146383802 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810642 | GAGGGAGGGAGGGAG[A/G]GAAAGAAGGAAGGAA | 57097 |
rs146495210 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PARP11 | GRCh38.p7 | 12:3842511 | CCATAGGGGACAGCA[A/C]GCTTGACGGTTGTTG | 57097 |
rs146578669 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PARP11 | GRCh38.p7 | 12:3851654 | AATGAGGCCTGCCTA[C/T]CTCTGTAGACTCCAC | 57097 |
rs146696731 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839994 | GTCAGGCAACGAGCA[C/G]CTGAAGAACAATGGG | 57097 |
rs146737575 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3870574 | GAGGGAAAATTCATA[A/G]TAGGAGCAAAGAATT | 57097 |
rs146749209 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PARP11 | GRCh38.p7 | 12:3865319 | GGAAAAAAATAAAAC[C/T]CATGTATTCAGCTGT | 57097 |
rs146845797 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3818663 | TTTGCTGTATACACA[A/G]TATGATGTCTACCAA | 57097 |
rs146857733 | snp | C/T | 4.94319e-05 | 0.00497127 | synonymous-codon, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812219 | CACACAGCTGTCATA[C/T]AAATTCACATAGCTC | 57097 |
rs147049870 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | PARP11 | GRCh38.p7 | 12:3841434 | CAAAGAGGCTCCTGC[C/T]GCCCAGAATTAAAGT | 57097 |
rs147086146 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, nc-transcript-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3871745 | AATACTCTTGGCAAA[C/T]AGATCCCACTCTCTG | 57097 |
rs147190995 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3816838 | ATCCAGGAGGCGGAG[A/G]TTGTAATGAGCTGAG | 57097 |
rs147199477 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PARP11 | GRCh38.p7 | 12:3852737 | AGGAGAACTTCCCCA[A/G]CCTAGCAAGGCAGGC | 57097 |
rs147200625 | snp | C/G | 0.00557542 | 0.0525036 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810861 | GAGGAGAGAAGAGGA[C/G]AAAAGGAAGAAAATC | 57097 |
rs147209402 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PARP11 | GRCh38.p7 | 12:3851445 | TTAGCAAATGGCACA[C/T]CAGGAGATTATATCC | 57097 |
rs147310298 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3850319 | CAGTTCGAACACCCC[-/T]AATCCAAAAATCTGA | 57097 |
rs147314883 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | PARP11 | GRCh38.p7 | 12:3838885 | GCTTCACCTGAGCCG[C/G]CCCGGCGTGCGCGCC | 57097 |
rs147407807 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810641 | GGAGGGAGGGAGGGA[A/G]GGAAAGAAGGAAGGA | 57097 |
rs147507495 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | PARP11 | GRCh38.p7 | 12:3837473 | TAAAAATAAAAACTA[A/G]TGAGTTAAAACATAC | 57097 |
rs147518262 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PARP11 | GRCh38.p7 | 12:3868415 | CAGTTAGCCGAGATC[A/G]TGCCACTGCACTCCA | 57097 |
rs147527891 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PARP11 | GRCh38.p7 | 12:3863022 | AATTATATCTTTCGA[C/T]TTATTTAGGTCTTAA | 57097 |
rs147572324 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PARP11 | GRCh38.p7 | 12:3857045 | AGAAAACCAAACACC[A/G]CACGTTCTCACTCAT | 57097 |
rs147770374 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3834963 | TCTGGCCAAACACGA[C/T]GTAACAGAAGCTACT | 57097 |
rs147876615 | snp | A/G | 0.0174175 | 0.0916809 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3811247 | TGTGTGTGCTGCAGA[A/G]GGGAAGGTAAAAAAA | 57097 |
rs147887780 | snp | C/G | 0.00914312 | 0.0669923 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3875303 | ATGAAAAAATGTCTT[C/G]TTAGTTCTAATAGCT | 57097 |
rs147898160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3871718 | AGGCAGTTTCAACCA[C/T]AACAACAGAAGAATA | 57097 |
rs147917931 | in-del | -/GACA | 0.126909 | 0.217598 | intron-variant | PARP11 | GRCh38.p7 | 12:3864008 | TGGAGGTGAGCAAAG[-/GACA]GTCATGGAAACAAGC | 57097 |
rs147958494 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3860179 | ATTTGATAAGATTAG[A/C/T]ATGGATGTGGACCGC | 57097 |
rs148002318 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PARP11 | GRCh38.p7 | 12:3816004 | AAATTTAAATGTATA[C/T]GCTTTGATCTATTTG | 57097 |
rs148054221 | snp | A/G | 0.00109355 | 0.0233576 | intron-variant | PARP11 | GRCh38.p7 | 12:3822170 | TAACTTGAAACAGCA[A/G]AAGAGAAAACAAAAT | 57097 |
rs148065105 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | PARP11 | GRCh38.p7 | 12:3855869 | TCATGCTACCTGATT[G/T]CAAACTATACTAAAA | 57097 |
rs148098618 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3867326 | ATGTTGCAGAAGGAA[A/G]TGGCAGCGTTTGCAA | 57097 |
rs148160228 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PARP11 | GRCh38.p7 | 12:3845722 | TTTAGAATCCTAATA[A/G]TGTCTCATTTCCAAT | 57097 |
rs148214469 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3850637 | CAATATCTATGTGCA[C/T]TACTGTGTTTTTTTC | 57097 |
rs148338166 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PARP11 | GRCh38.p7 | 12:3862628 | AATTTTTATAGTATA[C/G]CAAAGTATGGAGTGA | 57097 |
rs148362705 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PARP11 | GRCh38.p7 | 12:3843070 | AGGCCTTTCATCTCG[A/G]TATCTGTCAAACTTG | 57097 |
rs148390723 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3869717 | CCCCCTACACTGTCA[C/T]AGTACTCTTTTTCTT | 57097 |
rs148444216 | snp | A/C | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3873830 | ATTTGCTCACAAGGG[A/C]ACCTTTACATACTAT | 57097 |
rs148495129 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3811280 | TCTTAGAAGTGATCA[C/T]TGTAGGGACTCTTTT | 57097 |
rs148532530 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | PARP11 | GRCh38.p7 | 12:3851586 | TTGCTGAGGCTTGAG[C/T]AGGTAAACAAAGTGG | 57097 |
rs148539574 | snp | A/C | 0.046775 | 0.145601 | intron-variant | PARP11 | GRCh38.p7 | 12:3859086 | CTGGGCGACAGAGCA[A/C]GACTCCATCTCAAAA | 57097 |
rs148563477 | snp | A/T | 0.00016544 | 0.00909354 | utr-variant-5-prime, missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3829996 | GTTTTAGAAAATAAT[A/T]CTTCTGCTTTGTGAA | 57097 |
rs148739302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3817870 | AAATGTCAGAACCCA[A/G]AGGTTCTGATTCAGT | 57097 |
rs148747146 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PARP11 | GRCh38.p7 | 12:3834304 | GACTGACTTTATTTG[A/G]AACAGAGAGCAGAAC | 57097 |
rs148824630 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | PARP11 | GRCh38.p7 | 12:3852166 | AGGTAGATAAAACCA[C/T]AAAGATGGGGAAAAA | 57097 |
rs148857990 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3860552 | TTCATTTTGTAGCCT[A/T]AAGATTTCATGGAAC | 57097 |
rs149059206 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3820275 | TATTGCTGGATGGAC[G/T]CACGTGGGCCTGACT | 57097 |
rs149066891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3835272 | ATCCAGAAATGCCAC[A/G]TAAGTAGTCAGGTTA | 57097 |
rs149118556 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3840757 | TTGGATAAAAGACCC[A/G]AACCAAGCATATTGG | 57097 |
rs149180300 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3809955 | TTGTTTCAAAGTATT[C/G]TACATGCAATGTCCT | 57097 |
rs149216493 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PARP11 | GRCh38.p7 | 12:3824580 | CCCTATTGTATCTTA[C/T]CTAAACAGTCCTCTC | 57097 |
rs149236326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3814681 | CATCCAGTTTAATCC[C/T]CTTCCCAAGGATAAA | 57097 |
rs149290429 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | PARP11 | GRCh38.p7 | 12:3846795 | AAAAGAAATAGAAAA[C/T]TTGAATAGGATGGGT | 57097 |
rs149342138 | in-del | -/AT | 0.0283406 | 0.115616 | intron-variant | PARP11 | GRCh38.p7 | 12:3849924 | TTATTAAATTATCAC[-/AT]GTCCTGAAAATATGT | 57097 |
rs149385779 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3836920 | GAAAAAGTGAGATTA[A/T]GGTGGCCAACCAGCT | 57097 |
rs149437678 | snp | C/G/T | 4.94444e-05 | 0.00497194 | missense, synonymous-codon, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3829890 | AAGGAAAGGAGGTAC[C/G/T]TGAAACATGTGCCAC | 57097 |
rs149451448 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3872585 | CACCGAACGAAAACA[C/T]CTAAGAACATACAGT | 57097 |
rs149503127 | snp | A/T | 0.0142736 | 0.0832652 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810747 | GAAAGAGGAAGAGAA[A/T]AAGGAAGAGAGAGAA | 57097 |
rs149535590 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3826923 | CTTAATGTAAGATTC[C/T]AGCCAGTTTATCTCA | 57097 |
rs149598747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3862307 | AAAATTTAAAAATTA[A/G]CTGGGCATGGTAGCA | 57097 |
rs149651455 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3869284 | ATATCTTTAGGAGGC[C/T]ATTATTACGTCTACC | 57097 |
rs149705634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839977 | AATGGATTTAAACCT[C/T]TGTCAGGCAACGAGC | 57097 |
rs149765424 | snp | A/G | 0.021333 | 0.101051 | intron-variant | PARP11 | GRCh38.p7 | 12:3851522 | CTAGCGCAGCAGTCC[A/G]AGATCAAACTGCAAG | 57097 |
rs149768449 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3874609 | TTATGCGTATACTAC[A/G]TACACACAAATAGAC | 57097 |
rs149828341 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PARP11 | GRCh38.p7 | 12:3829481 | TCACTTTCCTTGACT[A/G]TAAGACAGAATGTTA | 57097 |
rs149849672 | in-del | -/T | 0.0263992 | 0.111815 | intron-variant | PARP11 | GRCh38.p7 | 12:3846271 | AACTGTGTGCATATA[-/T]TTTAAAAAAAAAAAG | 57097 |
rs149917237 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3864841 | ATAGTCTTGATGTTC[C/T]CAAAGAACTAGCTTT | 57097 |
rs149944403 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3871206 | TACTGATTATAGGAA[A/C]TTATTGCAAATATGG | 57097 |
rs149975559 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PARP11 | GRCh38.p7 | 12:3817574 | CTGCAAGGAAAGTCA[C/T]AGAACTACACTAAGT | 57097 |
rs149986308 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PARP11 | GRCh38.p7 | 12:3853726 | TATTAGATAGATCAA[C/T]GAGACAGAAAGTTAA | 57097 |
rs150039548 | snp | A/G | 0.118933 | 0.212888 | intron-variant | PARP11 | GRCh38.p7 | 12:3856699 | TAGTTCAACCATTGT[A/G]GAAGATGGAAGACAC | 57097 |
rs150083788 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | PARP11 | GRCh38.p7 | 12:3852032 | CTCCAACAGACGTGC[A/C]GCAGAGGAACCTGAC | 57097 |
rs150162176 | in-del | -/A | | | intron-variant | PARP11 | GRCh38.p7 | 12:3849267 | TTATGGAGGTACCTC[-/A]AAAAAAAAATAGAAC | 57097 |
rs150198125 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3836755 | CAAATATTATGTAGG[C/G]AGAGACAGTTCCCAG | 57097 |
rs150209207 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | PARP11 | GRCh38.p7 | 12:3867842 | TGGTTGAAACATTCA[C/T]CCTAATATTACAGGC | 57097 |
rs150261985 | snp | A/C | 0.0271762 | 0.113356 | intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3872194 | GACCTTGCTGGGCTT[A/C]CTTCCTCAGTTTATT | 57097 |
rs150293636 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3820074 | GGGTCCCCTCACTTT[C/G]TGCTCCCATGACTCC | 57097 |
rs150345549 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PARP11 | GRCh38.p7 | 12:3826575 | TTAGGAAAGCTAAGA[A/G]TACTAGAAAGAGAGA | 57097 |
rs150356015 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3858080 | ACTATGTTCAGTGTT[A/G]ATGATGAACAATTGG | 57097 |
rs150409913 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | PARP11 | GRCh38.p7 | 12:3862154 | TTTTCTCAGCCAGGC[A/G]TAGTGGCTCATCCCT | 57097 |
rs150441113 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | PARP11 | GRCh38.p7 | 12:3808470 | ATGGTAGACACAGTG[C/T]GAGTGGCTGGAGGTT | 57097 |
rs150452650 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3848578 | TCAATAAATGGTGCT[A/C/G]GGAAAACTGAATAAA | 57097 |
rs150528667 | snp | A/G | | | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3870112 | TCATATTTTCAGACC[A/G]CAGCTGACTTCTGGT | 57097 |
rs150612292 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3822887 | CTCAACCATTCATTC[G/T]ATGTTCTCCAAGTTC | 57097 |
rs150666692 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | PARP11 | GRCh38.p7 | 12:3828697 | ACAATCTTCACATAC[A/G]TTAATATATACAAAC | 57097 |
rs150728174 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PARP11 | GRCh38.p7 | 12:3864324 | TTATATATGTTAGAT[C/T]TGAGTTGCTAAAATT | 57097 |
rs150770671 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | PARP11 | GRCh38.p7 | 12:3851265 | GGACTGGTTGGGCAG[C/G]GGGTGCAGCCCACAG | 57097 |
rs150884947 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | PARP11 | GRCh38.p7 | 12:3834704 | ATTAAGAAAGGCTAG[C/G]AGCTCCAATATAAGC | 57097 |
rs150958160 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | PARP11 | GRCh38.p7 | 12:3831863 | CCTACTGCTTTTTTT[A/T]ATTAATGTTCATTTC | 57097 |
rs150989890 | snp | A/G | 4.94523e-05 | 0.00497229 | synonymous-codon, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3814113 | TGCTTCCACAAATTC[A/G]CTGCTGGTACCATGA | 57097 |
rs150994524 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PARP11 | GRCh38.p7 | 12:3860908 | GTCTTCAACTCCTGG[C/T]CTCAAGTGATCCTCC | 57097 |
rs151003151 | snp | A/C | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3874190 | CCTATAGATTTAGAA[A/C]CTGATTTTTTTTTCA | 57097 |
rs151109323 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PARP11 | GRCh38.p7 | 12:3819634 | AATGCAGATCAGATC[C/T]ATCACTCTCTTGCTT | 57097 |
rs151118768 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | PARP11 | GRCh38.p7 | 12:3854603 | AGAGGTTGAATCCCT[A/G]AATAGACCAGTAACA | 57097 |
rs151172354 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3857490 | CAGCTGCTGAGACAG[A/C]CTTTACAGGAATTAA | 57097 |
rs151266364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3848438 | GTAATCAAATCAGCA[C/T]GATACTTGCATAAAA | 57097 |
rs151327711 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PARP11 | GRCh38.p7 | 12:3824659 | CTTGTGCTGTCTTTG[C/T]TCTATGGTTTGTACA | 57097 |
rs180800101 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3849198 | GAAAATGGAACCCTC[A/G]TTCACTGTTGGTGGG | 57097 |
rs180806440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3830851 | GGCTTCAGGGTCTAC[A/G]CACTTAGCCGCCGTC | 57097 |
rs180815594 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PARP11 | GRCh38.p7 | 12:3868955 | TCAAGGTGAGTTTGA[C/T]TCCCTTCTAAAGGTT | 57097 |
rs180818022 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PARP11 | GRCh38.p7 | 12:3821376 | AGTCACCCAACTTAA[C/T]GGGTCATTTCCCACT | 57097 |
rs180822067 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810491 | GTAACTGGAGAAGCT[A/G]AGGCAAGAGAATTGC | 57097 |
rs180939809 | snp | A/T | 0.0193772 | 0.0965046 | intron-variant | PARP11 | GRCh38.p7 | 12:3844529 | TCTCAGGAGTCCAAA[A/T]TAAGTTGTTGCTGCA | 57097 |
rs180941882 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3873422 | CTCCCGACTTCCGCC[C/T]GACGTTGGCCAGTCA | 57097 |
rs180953230 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3864198 | TACTGGAATCACCAC[A/G]TAGTTTTTCATTTTA | 57097 |
rs180967664 | snp | A/C | 0.00257333 | 0.0357777 | intron-variant | PARP11 | GRCh38.p7 | 12:3826123 | AGTAAGAAAAAAAAA[A/C]CCCACTCTTTCCACC | 57097 |
rs180969615 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3815276 | CATCACGTGCTCACT[C/T]TGCAAAACAGCACAA | 57097 |
rs181005954 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | PARP11 | GRCh38.p7 | 12:3835572 | GGTAGACTGGGCAAA[C/G]AAACACTTCAAAGCA | 57097 |
rs181034391 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3853369 | GTCAAGACCCATCAG[C/T]GTGCTGCATTCAGGA | 57097 |
rs181094949 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3869505 | TGTGTCCCAGCCACA[G/T]AGGCTTCTCTCTTTT | 57097 |
rs181095974 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PARP11 | GRCh38.p7 | 12:3819716 | GTTTAGCTTATAAGG[A/C]CCCACGTGGTCTAGC | 57097 |
rs181099684 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3811383 | ACAGCAAGTCGTGGT[A/G]TAAGAATCCAAGAGC | 57097 |
rs181100046 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | PARP11 | GRCh38.p7 | 12:3849447 | AAGAAAATGTGGTTT[A/T]TATACACAATGGATT | 57097 |
rs181104476 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PARP11 | GRCh38.p7 | 12:3856667 | AACACTTTTACACTA[C/T]TGGTGGGAGTGTAAA | 57097 |
rs181114868 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3838882 | CCCGCTTCACCTGAG[A/C]CGGCCCGGCGTGCGC | 57097 |
rs181170174 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | PARP11 | GRCh38.p7 | 12:3831636 | GTTATTTTTTATATA[A/T]GTTTGGAAACTCAAG | 57097 |
rs181401672 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3874524 | TTGGCCTCCCAAAGT[G/T]CTGGGATTACAGGTG | 57097 |
rs181555512 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3862575 | TAAATTTTTCTATAC[C/T]ATATATTTTATTAGT | 57097 |
rs181581685 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PARP11 | GRCh38.p7 | 12:3825294 | TTTTCAGACTTCTTA[C/T]GGCCAGAGCAAGCAA | 57097 |
rs181592660 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PARP11 | GRCh38.p7 | 12:3844159 | TGTAACTGCTGATTT[A/G]AGTAGTGATTAGCAT | 57097 |
rs181684283 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PARP11 | GRCh38.p7 | 12:3857257 | GTTGTGCACATGTAC[C/T]CTGGAACTTAAAGTA | 57097 |
rs181695953 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | PARP11 | GRCh38.p7 | 12:3854262 | AATTCAAAAGCTAGC[A/G]GAAGGCAAGAAATAA | 57097 |
rs181697504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3815883 | GAGTTCTGTAAATGA[C/T]AGGCAGCTCGTTGAA | 57097 |
rs181710747 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839966 | CTGCTGATGTGAATG[C/G]ATTTAAACCTTTGTC | 57097 |
rs181719216 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3820194 | GTGCTTGTCATAAAG[G/T]AGGTACTAAGACATT | 57097 |
rs181790147 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | PARP11 | GRCh38.p7 | 12:3830392 | ACGCTGGTTAAGATC[A/T]AATGCATCTAATTTT | 57097 |
rs181819205 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3836233 | CAACTGATCACATAT[A/G]AGAGAATCCTAATGA | 57097 |
rs181985960 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3844349 | GTTGTTGAAGGTACC[A/G]CTTAAGCCATTTCTT | 57097 |
rs182025699 | snp | A/C/G | 0.0314385 | 0.121371 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3809707 | AATTACAAATAAATC[A/C/G]AAAAAAAGATTTTCA | 57097 |
rs182154966 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PARP11 | GRCh38.p7 | 12:3858545 | TTCCTCGCCCCTATA[A/G]GAGCCACTACTTGGT | 57097 |
rs182201498 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3825843 | ACCATTCTCCTGACT[C/G]AGCCTCCCGAGTAGC | 57097 |
rs182264350 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3863651 | GGTGAAGTCTAGAAG[A/T]AACCACATACAAGGT | 57097 |
rs182408089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3841716 | ACCCAATCCATTCTT[A/G]GGCCCAGTTCCTATT | 57097 |
rs182427374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3840644 | AGTAGCAATCCATGT[A/G]TCCAGAGAAAATCAT | 57097 |
rs182430236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3821749 | AGCCTTGAGACCAGG[C/T]CAAAATACGGCAAGA | 57097 |
rs182443541 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PARP11 | GRCh38.p7 | 12:3867352 | TGCAAGATTATTCTT[C/T]CCACGCAAGTTTGCT | 57097 |
rs182535257 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3837298 | GAGCGTAAGGCACCA[C/T]CTAGTGCTTAAAAGG | 57097 |
rs182548050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3844880 | TATTAATTAGTCCAC[A/G]GGATTTTGCCTTATG | 57097 |
rs182553075 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PARP11 | GRCh38.p7 | 12:3817460 | CCCACTACTCCCACT[A/G]CTAAGGCAGCCACGA | 57097 |
rs182563716 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3865103 | TTTCTCTTTTCATTT[A/C]TTTAATCCATGGGTT | 57097 |
rs182626128 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3871161 | TTCTAACTTATCTGG[A/C]AATATATTCCAGAAA | 57097 |
rs182683625 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3836864 | TCAGCCCAGCATCAA[G/T]CATACAGAAAACTTT | 57097 |
rs182840605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3813911 | TACACAATGCAATTA[C/T]AATCCATTTGTTTTA | 57097 |
rs182916265 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PARP11 | GRCh38.p7 | 12:3851006 | CATCAGCATCACAGA[A/G]AATCCATGCCACTTA | 57097 |
rs182951026 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PARP11 | GRCh38.p7 | 12:3817122 | CATGAACCCCGGAGG[C/T]GGAACTTGCAGTGAG | 57097 |
rs183004854 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3855185 | AATATCAAACTGAAT[C/G]AGCAAAAACTGGAAG | 57097 |
rs183026173 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PARP11 | GRCh38.p7 | 12:3854757 | TCAACAGAAAAAAAG[A/G]GAATCCCCCCTAACT | 57097 |
rs183039841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3841899 | TTCAGTTTCCACAGT[A/G]GATGAGTTTCCAGCA | 57097 |
rs183046476 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3827150 | TTTAGTTTACTTTTC[A/C]CCATTTTTATAGAGA | 57097 |
rs183050316 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PARP11 | GRCh38.p7 | 12:3822365 | GCACTTTGGGAGGCC[A/G]AGGCGAGCGGATCAC | 57097 |
rs183059380 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PARP11 | GRCh38.p7 | 12:3859381 | CAACTTGACCAACAC[A/G]GTGAAACCCTGTCTC | 57097 |
rs183139830 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PARP11 | GRCh38.p7 | 12:3833497 | TAGTCCTAGCCCCTT[G/T]AGAGGCTGAGATGGA | 57097 |
rs183144769 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PARP11 | GRCh38.p7 | 12:3859160 | GTGTAAAAGGCATAT[A/G]TGAAACAAATAAATT | 57097 |
rs183260817 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3875166 | ATCACATAGGTTTGC[A/G]TAATCCTTGGGAAGT | 57097 |
rs183265684 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3854598 | CAGGAAGAGGTTGAA[C/T]CCCTGAATAGACCAG | 57097 |
rs183287302 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PARP11 | GRCh38.p7 | 12:3836551 | AAGAAAAGAGCGCTG[A/G]TAAAAGGTATAATTG | 57097 |
rs183288303 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3816899 | AGAGCAAGACTCCAT[C/T]TCAAAAAGAAGGCCA | 57097 |
rs183374469 | snp | C/T | | | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3870572 | AGGAGGGAAAATTCA[C/T]AGTAGGAGCAAAGAA | 57097 |
rs183404406 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3850568 | GTAATAAAATGGTAT[A/T]TGTACAGGCTGGATA | 57097 |
rs183409314 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3813221 | TGGAAACCGATGGCC[C/T]ACAGGGATTCTTTTA | 57097 |
rs183410706 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3833045 | GTTTAAAGTCAAAAT[C/T]CTGGTCTATATAAGG | 57097 |
rs183538045 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3832086 | CAGCATACATATAAC[A/G]TGTGTGCTCCGCTAT | 57097 |
rs183622620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3870292 | TAGTAATAAAATACA[A/G]TAGCAGTAAGACAAA | 57097 |
rs183713816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3846059 | CTTGTAAAAAAAGTA[C/T]ATATACGTATCTTTT | 57097 |
rs183780981 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PARP11 | GRCh38.p7 | 12:3811881 | AATGGTATCTTTCAC[A/C]CCTATGTGTTAAAAC | 57097 |
rs183782305 | snp | A/G | 0 | 0 | intron-variant | PARP11 | GRCh38.p7 | 12:3850274 | GGGTTGGTAACATAT[A/G]TAGACATAATATATA | 57097 |
rs183927329 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3827631 | AATGGCTTGTCACGA[C/G]CAAGGATCTAATGGT | 57097 |
rs183964096 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PARP11 | GRCh38.p7 | 12:3846348 | ACTGAGACCACAAGA[A/T]ATACAAAGAATTATT | 57097 |
rs183964425 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | PARP11 | GRCh38.p7 | 12:3808589 | AAAAAATGCTGCAGA[C/T]GCCAACTCTTGGCCT | 57097 |
rs183993330 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PARP11 | GRCh38.p7 | 12:3865995 | TTGGTGGCTTATTAA[C/T]TGTAACTCTTTGTCT | 57097 |
rs184076737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3861607 | TAAATACTTTCTCCC[A/G]TCTGTGGCTTATCTT | 57097 |
rs184110387 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3842905 | ACTAAAGTGACAAGA[A/T]AATACACCATTTGAC | 57097 |
rs184113560 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3825133 | TTTCCAGTTTCATTT[A/T]AAATTATTTGAACAA | 57097 |
rs184231454 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3856745 | AGGATCTAGAACTAG[A/T]AATACTATTTGACCC | 57097 |
rs184247914 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3868231 | TTTGGGAGGCCTAGG[C/G/T]GGGTGGATCACTTGA | 57097 |
rs184263066 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3838906 | CGTGCGCGCCTGGGG[A/C]GGGGCTTTTCTCGCT | 57097 |
rs184372203 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3863516 | AGGGGTCCCTAAGAC[A/C]ACCCTCAGGGTTGAT | 57097 |
rs184492164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3814497 | ACCAGCTAACCTTTA[C/T]AGATGCCTAAAAATG | 57097 |
rs184501842 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3838322 | ACTACACAAAAACAT[G/T]GAAATTAAACAACAT | 57097 |
rs184573920 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3818524 | AGGTCCTTTCCAATT[A/G]CAATGTTCAGTTCTC | 57097 |
rs184638533 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810072 | TCCCTAATCTGTCTG[C/T]ACTCTTTGCTTTTAT | 57097 |
rs184639012 | snp | A/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3837913 | GGACATAATTATAAA[A/T]ATCTATGCACTCAAC | 57097 |
rs184647568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3819102 | ACTCCCTTTCCATCA[C/T]CCCTAAAGATGTCCC | 57097 |
rs184649513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3856315 | AGCACAAGAAACTAC[C/T]ATCAGAGTGAACAGG | 57097 |
rs184654888 | snp | C/T | 0.097727 | 0.198275 | intron-variant | PARP11 | GRCh38.p7 | 12:3856009 | TGATCTTTGACAAAC[C/T]TGACAAAAACAAGAA | 57097 |
rs184693206 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PARP11 | GRCh38.p7 | 12:3844247 | GGTGCTAGGTAAAAA[A/G]TTGTAAAGACTGGGA | 57097 |
rs184716466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3815117 | ATTGGTAGATACATG[A/G]GAGTCTGCAAACTAT | 57097 |
rs184773051 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PARP11 | GRCh38.p7 | 12:3835164 | CTATAATAGCAGCCA[A/C]CAAGCCACACACACA | 57097 |
rs184775821 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PARP11 | GRCh38.p7 | 12:3829612 | TCCCTTTCTCTTTGT[C/T]CACCAAACCAAACTT | 57097 |
rs184783415 | snp | A/G | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3873019 | AAACAATAAAGCATT[A/G]GAGAATCCACCCAGG | 57097 |
rs184786996 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3852436 | ACAGTGTAAGAGAAG[A/G]CCTTAAATGACCTGA | 57097 |
rs184904641 | snp | G/T | 0.00398564 | 0.0444627 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3808998 | TAAAACTTTCCTGTT[G/T]ATAACTAAAAGATTT | 57097 |
rs184907843 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PARP11 | GRCh38.p7 | 12:3849255 | AAAATTATGGAGGTA[A/C]CTCAAAAAAAAATAG | 57097 |
rs184916274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3831507 | GCTCTTCACAAAATG[A/G]AAAATGATAGACTCC | 57097 |
rs184924197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3869372 | AACATAAATATGTTC[A/G]TGACACTTCCTTCAA | 57097 |
rs184968072 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PARP11 | GRCh38.p7 | 12:3846634 | TGGTGGCAGGCGCCT[A/G]TAGTCCCAGCTACTC | 57097 |
rs185225123 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810670 | GAAGGAAGGAAGGAA[A/G]GAAGGAAGGAAGGAA | 57097 |
rs185330644 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3834493 | CAAAACATTAGCCAG[A/G]TGTGGTGGCGTGCAC | 57097 |
rs185340331 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | PARP11, LOC105369609 | GRCh38.p7 | 12:3872503 | CACATGAAGTCATAA[G/T]GAAAATACCAGAGTC | 57097 |
rs185442337 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PARP11 | GRCh38.p7 | 12:3825574 | AGTTTAGAGCAGAGA[C/T]CATAAGGCATTTTGT | 57097 |
rs185442711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3851864 | CCTCCCAGTAGGGGC[C/T]GACTGACACCTCATA | 57097 |
rs185451137 | snp | G/T | 0.0205511 | 0.0992634 | intron-variant | PARP11 | GRCh38.p7 | 12:3844530 | CTCAGGAGTCCAAAA[G/T]AAGTTGTTGCTGCAT | 57097 |
rs185459268 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3827088 | GCAAGATCATCTCAG[C/T]ATGTGGAGCAAGACC | 57097 |
rs185462809 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3848231 | AAATGACAATACTGC[A/C]CAAAGCAATTTACAG | 57097 |
rs185467401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3864692 | TCATACTGCTTGATA[C/T]AAAGTTGTTCATAAC | 57097 |
rs185570107 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3860494 | AGAGGGTCCAGAAGG[C/T]AGCACTTCCACTTCT | 57097 |
rs185572472 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PARP11 | GRCh38.p7 | 12:3823714 | TGAGCTTAGGAGTTC[A/G]AGACCAGCCTGGGCA | 57097 |
rs185612402 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3868615 | ATCTTCCATATGGCT[C/T]AGTGAAAACATCTTA | 57097 |
rs185627288 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3830534 | CTTACTCCTGTGAAC[A/G]TGCCTGTATCTGTGT | 57097 |
rs185708398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3842262 | GAAAATGAAAATGAA[A/G]TGTCATATTTTGAGA | 57097 |
rs185764912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3841526 | TGCTACAGCCAGTGA[C/T]TGGACCGCCGACATT | 57097 |
rs185794053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3819731 | CCCCACGTGGTCTAG[C/T]CCCCGCTAACTCTCT | 57097 |
rs185886297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3858612 | AAATACAGTGTATAG[A/G]AGCATTTTAATCAAA | 57097 |
rs185915790 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3821477 | ATGTTTTAAAGTGTT[A/C]TTTAAAATAAAACAG | 57097 |
rs185941561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3816042 | CTTTTCAGACCATTA[A/G]GCATGACATCAGAAG | 57097 |
rs185945840 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PARP11 | GRCh38.p7 | 12:3836340 | TAAAAAACAAACAAA[A/C]AAAAAGCGCCTATCA | 57097 |
rs186266323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3815601 | AATGTTGGCATGAAA[C/T]AGCAACAGTCCAGAT | 57097 |
rs186273753 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PARP11 | GRCh38.p7 | 12:3854143 | TTAAAGTAGTGTGTA[A/G]AGGGAAATTTACAGC | 57097 |
rs186370009 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3840419 | AGCCAATAAAAGCCC[C/T]ATTAGCACTACCTCC | 57097 |
rs186398300 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3832031 | TTCTATCTTTTCTCT[A/G]TTAGAAAAGAGAATA | 57097 |
rs186417966 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3835603 | ATTATTACAAATATG[C/T]TCAAAGACATAAATG | 57097 |
rs186420251 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3832518 | GTTGCTAACATTTAG[C/T]TTAATTGCTTTGCTT | 57097 |
rs186426263 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3857286 | TATAATAATAATAAT[A/T]AAAAAAAGATACAGC | 57097 |
rs186432451 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812064 | CTAGATGACTGAAGA[A/G]CAAACCTTCCTGCAA | 57097 |
rs186490518 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3836593 | TTTCCTCTCTTGACT[G/T]ATTTACAAGTAACTA | 57097 |
rs186494017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3869663 | TAAAAGTTACTTTCA[C/T]AGGGTGGCCTTTCCT | 57097 |
rs186494797 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | PARP11 | GRCh38.p7 | 12:3816943 | ACGCCTGTAATTCCA[C/G]CACTTTGGGAGGCTG | 57097 |
rs186525827 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3873668 | CCAAGAGTCACACAG[A/G]CCTGGCAATGGCATT | 57097 |
rs186537226 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3854645 | TCAGGCAATAATTAA[C/T]AGCCTACCAACCAAA | 57097 |
rs186537825 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3874900 | ACATAGGTATACATA[A/C]ACGTATATATCTGTT | 57097 |
rs186622236 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3833171 | GTATCTTCAGGAAAT[A/C]ATATTTGGTAATAAC | 57097 |
rs186622593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3813523 | CATATTTACCTAACA[C/T]TGATGGGATTTATGT | 57097 |
rs186626469 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PARP11 | GRCh38.p7 | 12:3849724 | GATATAAGAAATAAG[A/G]CCTAGAAGTGATAAG | 57097 |
rs186652380 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3811466 | ATGTGGGAGACAGAG[A/G]AGAATGACAGGATCA | 57097 |
rs186669008 | snp | C/T | | | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3870770 | CTTGAGTAAGACATA[C/T]ACTTGGGTGGCTAAA | 57097 |
rs186676482 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3850596 | ATACGCCAATGGCAG[A/G]TTCCTCACAATGCCC | 57097 |
rs186816459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3854513 | CTATGAACACCTCTA[C/T]GCAAATAAACTAGAA | 57097 |
rs186819890 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PARP11 | GRCh38.p7 | 12:3867702 | GTGAGACTGATTACA[C/G]TATTGTGTGTATAAA | 57097 |
rs187071509 | snp | C/T | 4.94442e-05 | 0.00497188 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3822141 | GCATAGGGATGGCCT[C/T]GTTTTCACAGATGTA | 57097 |
rs187090750 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3820721 | AAAGGAGGCAGAGGC[C/T]TCTGTCTTCCTCTAT | 57097 |
rs187118521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3828237 | CTTTCTCACTTAACA[C/T]CTGTTTGATCCTTAA | 57097 |
rs187125194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3846452 | ATCTACTATGATTAA[A/G]TCATAAAGAAATAGA | 57097 |
rs187127830 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | PARP11 | GRCh38.p7 | 12:3808763 | AAACTCCTTGGGTCC[A/G]CTAAGATTGAGCTGA | 57097 |
rs187141738 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PARP11 | GRCh38.p7 | 12:3841760 | TTCCTCATGTTTGGC[A/G]TGGGTACCCTTTTCA | 57097 |
rs187156169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3859179 | AACAAATAAATTCAT[A/G]TTTAGACTTGGGTAC | 57097 |
rs187176246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3850295 | ATAATATATATAGCA[C/T]AATTATATCAGTTCG | 57097 |
rs187208214 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3817803 | TGCCTAGATTTAGAA[A/C]ACCTGTCATCCTGCT | 57097 |
rs187215577 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3865126 | CATGGGTTACCTTAA[A/G]GTGTTATTTATTTAC | 57097 |
rs187272626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3837506 | CCAGAGAAAATCACT[C/T]AACCAGAAAGGAAGA | 57097 |
rs187276473 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3863689 | GTCCCTTCCCGGTGC[A/T]GTCACATGGGACACA | 57097 |
rs187285013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3855708 | ATACTGCCCAAGGTA[A/G]TTTATAGATTCAATG | 57097 |
rs187299646 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | PARP11 | GRCh38.p7 | 12:3825951 | TAGCCAAGATGGTCT[C/T]GATCTCCTGACTCGT | 57097 |
rs187344506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3870293 | AGTAATAAAATACAG[C/T]AGCAGTAAGACAAAT | 57097 |
rs187462512 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PARP11 | GRCh38.p7 | 12:3844352 | GTTGAAGGTACCGCT[G/T]AAGCCATTTCTTTCT | 57097 |
rs187515655 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PARP11 | GRCh38.p7 | 12:3842574 | GAATGTTTCTGAAGG[C/T]TTTAAAAAACTACAA | 57097 |
rs187731425 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3859533 | CACCACTGCCCTCCA[A/G]CCTGGGTGACAGAGT | 57097 |
rs187737883 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3860801 | TGTGCTTCAGCTTCC[A/T]GAGGAGCTGGGACTA | 57097 |
rs187764345 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3824428 | CAAAAAATTTTTTTA[C/G]TTTTTATGTAGTCAA | 57097 |
rs187875981 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3856101 | TGGATCCCTTCCTTA[C/T]ACCTTATATAAAAAT | 57097 |
rs187936943 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PARP11 | GRCh38.p7 | 12:3854813 | GATACCAAAGCCTGG[C/T]AGAGAAACAACAAAA | 57097 |
rs187958928 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PARP11 | GRCh38.p7 | 12:3817312 | GTTAAAGGGCATGGA[A/G]TATGGGCATAGGCAG | 57097 |
rs188007515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3835329 | TCAGAAGCTACACAC[C/T]GTGAGGAAAATGGAC | 57097 |
rs188018948 | snp | A/C/T | 0.0115187 | 0.075054 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3873370 | GCCTTCCTCCTCCCC[A/C/T]TCCCTGTCACAAGCC | 57097 |
rs188027097 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PARP11 | GRCh38.p7 | 12:3852537 | GGAAGAAAGGGTATC[A/G]GTGACTGAAGATCAA | 57097 |
rs188102976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3871231 | ATATGGAAATTAGGG[A/G]TTATTAAAGTAAATT | 57097 |
rs188118874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3833981 | TGACACAGAGGACCC[A/G]TCTCTCTTTCCCTAC | 57097 |
rs188163367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3831538 | TTCCTCATTGGGATG[C/T]TGTTATAAATGAATG | 57097 |
rs188175176 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3869430 | TTCAAAATCCTAAAC[A/G]TGTGCCTCAAATCCA | 57097 |
rs188180769 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3849443 | GATAAAGAAAATGTG[G/T]TTTATATACACAATG | 57097 |
rs188199904 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3845371 | CTTATTTAATGCAGA[A/C]TGTATTCTTGCAGTG | 57097 |
rs188251882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3837200 | CAAGTCAGCCTTCCC[A/G]CACTGCCAGGATAAC | 57097 |
rs188370607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3851011 | GCATCACAGAGAATC[C/T]ATGCCACTTAATAGT | 57097 |
rs188388588 | snp | C/T | 1.68238e-05 | 0.00290028 | intron-variant | PARP11 | GRCh38.p7 | 12:3814024 | AAATTGGACCTGGAA[C/T]TCTGATAATTACCTT | 57097 |
rs188480846 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PARP11 | GRCh38.p7 | 12:3827288 | GGGGAACTCCAGTTA[C/T]TAGTATATGTAACTC | 57097 |
rs188791463 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3843758 | ATTAACACAGTATTC[A/T]TTCATCTGTGTTATT | 57097 |
rs188797525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3825219 | TAAGATTTTTTCCTT[C/T]AAGTCCATTCATTCA | 57097 |
rs188856983 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PARP11 | GRCh38.p7 | 12:3861703 | ACTTTTTTTTTTCAT[C/T]GATCATAGTCCTGGC | 57097 |
rs188888223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3866677 | TTTCACACAAAGCAC[A/G]AAGTCCATTTGCTTT | 57097 |
rs188923529 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PARP11 | GRCh38.p7 | 12:3828144 | TGTCCATTAAAGAAA[C/T]TGTTTTCTGACAAAG | 57097 |
rs188940547 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839442 | CGGGTCGTGCCTGTT[C/T]CGGGCCGTGGCGGAG | 57097 |
rs188944656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3819920 | TGCTTCAATTTTCTG[C/T]GCTCCCTCTTATATC | 57097 |
rs188962477 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PARP11 | GRCh38.p7 | 12:3851882 | CTGACACCTCATACA[C/G]TCGGATGCCCCTCTG | 57097 |
rs188973241 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | PARP11 | GRCh38.p7 | 12:3834541 | CAGGAGGCCGAGAGA[A/G]GAGAACTGATTGAAC | 57097 |
rs189005231 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PARP11 | GRCh38.p7 | 12:3842097 | AGAGAGAGAGAAATT[A/G]TGCCTGTTGAACTTG | 57097 |
rs189008494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3856780 | ATTTCATTACTGGGT[A/G]TATACCCAAAGGATT | 57097 |
rs189056932 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PARP11 | GRCh38.p7 | 12:3815267 | TACTCACAGCATCAC[A/G]TGCTCACTTTGCAAA | 57097 |
rs189198938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3846061 | TGTAAAAAAAGTATA[C/T]ATACGTATCTTTTGA | 57097 |
rs189208678 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | PARP11 | GRCh38.p7 | 12:3856329 | CCATCAGAGTGAACA[C/G]GCAACCTACAGAATG | 57097 |
rs189212908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3819403 | TGGACACTTCTTTGT[C/T]GTGAAAGGCTTCTTC | 57097 |
rs189279270 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3814950 | ATGTAGGTATACATA[A/C]ACAGGTAGTAAAAAA | 57097 |
rs189366874 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3853099 | GAGAGATTTTTGTCA[C/T]CACCAGGCCTGCCTT | 57097 |
rs189425913 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | PARP11 | GRCh38.p7 | 12:3837928 | TATCTATGCACTCAA[C/G]ACCCAAGATCTTAAG | 57097 |
rs189427708 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810321 | CAGGCCGGGTACAGC[A/G]GCTCATGCCTGTAAT | 57097 |
rs189435393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3830632 | CAGTTTTTCTAAGTG[C/T]CAGGATACAATAACA | 57097 |
rs189505529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3838463 | AGCAGTACTAAAAGA[A/G]AAGTTTATAGCAATA | 57097 |
rs189576232 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3825953 | GCCAAGATGGTCTCG[A/C]TCTCCTGACTCGTGA | 57097 |
rs189748062 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810806 | AGAGGAAGACAGAAG[A/G]GAAGAGAAAGAAGAG | 57097 |
rs189753501 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3874183 | AAGAATACCTATAGA[A/T]TTAGAACCTGATTTT | 57097 |
rs189756143 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PARP11 | GRCh38.p7 | 12:3854649 | GCAATAATTAATAGC[C/T]TACCAACCAAAAAAA | 57097 |
rs189768846 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3836177 | TCAAAATTTCGAAAG[A/C]CAAAGACAAACAGAA | 57097 |
rs189849389 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3847402 | TATCACCCATGTACA[C/T]AGATGCAAAAATCCT | 57097 |
rs189890309 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3809065 | CAAGGTGAAAAAGAA[A/T]AGTCATTATCAGCTG | 57097 |
rs189987124 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3863627 | TCAGCAAAGGGGAAA[C/T]GCACATGGGGTGAAG | 57097 |
rs190017445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3825763 | GAGTCTCACTCTGTC[A/G]CCCAGGTTGGAGTGG | 57097 |
rs190033990 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3815641 | CAGCACTGACTCCAC[C/T]GACACCACTGAATGT | 57097 |
rs190037444 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PARP11 | GRCh38.p7 | 12:3854199 | GAAAGATCTAAAATC[A/G]ACACCCTAACATCAC | 57097 |
rs190097291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3868452 | GTGACAGACTACCTA[C/T]AGACACTGAGGCTCA | 57097 |
rs190125345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3830226 | CAATTTAGGCAAGTA[A/G]TAATAATCTTAGGTA | 57097 |
rs190252961 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3844325 | GTTGTCACCTTCTAA[A/G]CTAGAATAGTTGTTG | 57097 |
rs190256208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3844544 | ATAAGTTGTTGCTGC[A/G]TTTTATTGACTGGGG | 57097 |
rs190268794 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3827128 | ATCTTCTTGGACCAT[C/T]TCATTTTTTAGTTTA | 57097 |
rs190269088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3864827 | CTAGAAATTTATTAA[C/T]AGTCTTGATGTTCTC | 57097 |
rs190278709 | snp | C/T | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3872826 | AGGCAGTCGGGAGGC[C/T]GAGGCACGACAATCG | 57097 |
rs190403173 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PARP11 | GRCh38.p7 | 12:3841873 | AATCTGGATCTGTCT[A/G]AAGATTGTGGTTCAG | 57097 |
rs190418299 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3859292 | AGATGTAGGCCGGTG[C/T]AGTGGCTCACGTCTG | 57097 |
rs190437102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3822219 | TTACTGTCAAGAACT[C/T]AGCCCTTCTTCAAAG | 57097 |
rs190581555 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PARP11 | GRCh38.p7 | 12:3868943 | AATGGGCTAAAATCA[A/G]GGTGAGTTTGATTCC | 57097 |
rs190656297 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PARP11 | GRCh38.p7 | 12:3816865 | TGAGATTGTGCCACC[A/G]CACTGCAGCCTGGGG | 57097 |
rs190658126 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3836444 | AACTGAGAGAATTCA[A/C]TGCTAGCAAACTTGC | 57097 |
rs190707959 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PARP11 | GRCh38.p7 | 12:3816974 | AGGTGGGCGGATCAC[A/G]AGGTCAGAAGATCCA | 57097 |
rs190710987 | snp | A/G | | | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3875004 | TATATTTGCCTTTTC[A/G]TAAAGGAACCTCTCC | 57097 |
rs190714019 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PARP11 | GRCh38.p7 | 12:3844422 | GTCCTCCACTTTCAG[C/T]TTATGCTTTTTTTTG | 57097 |
rs190721139 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3854579 | CACCCTCCCAAGACT[A/C]AACCAGGAAGAGGTT | 57097 |
rs190749123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3818592 | ATCCCACATTAGCTG[C/T]CTTCTCACATCTCTC | 57097 |
rs190788879 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PARP11 | GRCh38.p7 | 12:3821579 | TTAGCCAAGGAAGTC[A/G]TATCAACAAAGCTAA | 57097 |
rs190813858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3848667 | TCAAATCAAAATGAA[C/T]TAAAGACTTAAATCT | 57097 |
rs190856559 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PARP11 | GRCh38.p7 | 12:3859057 | GAGCCGAGATCATGT[C/T]ATTGCACTCGAGCCT | 57097 |
rs190972390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3836648 | GTTCCAAGATGGTGG[C/T]ACAGAAGAAAGCTGG | 57097 |
rs190979863 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3864130 | ATTCCTAGGCTGCTG[A/G]GAATTTTAATCAGGA | 57097 |
rs191111726 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PARP11 | GRCh38.p7 | 12:3841588 | GTGTCTGAAAGTCAC[A/G]GACAATTGTCTTACC | 57097 |
rs191188577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3858324 | CAGTGATAAAGATAA[C/T]ATTAACCATGCAGAG | 57097 |
rs191197142 | snp | A/C/T | 0.00914312 | 0.0669923 | intron-variant | PARP11 | GRCh38.p7 | 12:3850309 | ATAATTATATCAGTT[A/C/T]GAACACCCCTAATCC | 57097 |
rs191200932 | snp | C/T | 0.000806747 | 0.020068 | intron-variant | PARP11 | GRCh38.p7 | 12:3812477 | AAGCCAAGATTACTC[C/T]GAAGAATATATTAAA | 57097 |
rs191343654 | snp | A/C/T | 0.028053 | 0.115706 | intron-variant | PARP11 | GRCh38.p7 | 12:3846275 | TGTGTGCATATATTT[A/C/T]AAAAAAAAAAGAAAA | 57097 |
rs191351727 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PARP11 | GRCh38.p7 | 12:3828210 | CTTGAAACTATTGCC[A/C]GCTACCTATGACTTT | 57097 |
rs191479448 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3870923 | AGCACATTCTCATTA[G/T]TCTAAATTATTTTTG | 57097 |
rs191487416 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PARP11 | GRCh38.p7 | 12:3850646 | TGTGCATTACTGTGT[G/T]TTTTTCTTATTCTCT | 57097 |
rs191497396 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3824622 | ATCTTGCTTATTGTC[C/G]TCCATTCTGCTTAGT | 57097 |
rs191518200 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PARP11 | GRCh38.p7 | 12:3811763 | TTTCAACATTTATAC[A/G]AATAAGTCTATTTAA | 57097 |
rs191519700 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3833397 | CATGAGGCCAGGAGT[A/T]TGAGGCAAGCCTGGC | 57097 |
rs191524824 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3850074 | GAAGGCAGGTGGGAA[A/C]AAAGCTATATTGGAG | 57097 |
rs191619519 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3867742 | TAAATGTTAAAACAA[A/G]ACATGGGAAAATACT | 57097 |
rs191624466 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PARP11 | GRCh38.p7 | 12:3846475 | GAAATAGAAAACTTG[A/G]ATTGGGCGCAGTAGC | 57097 |
rs191637032 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PARP11 | GRCh38.p7 | 12:3828479 | CTTGAACCCGGGAGG[C/T]GGAGGCTGCAGTGAG | 57097 |
rs191679847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3865346 | CTGTTGATGGGTGAA[C/T]TGTTCCATAAATGCC | 57097 |
rs191685414 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | PARP11 | GRCh38.p7 | 12:3827321 | ATTCCTTAATAATGA[C/T]ATTTTTAATAAACTC | 57097 |
rs191746460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3869801 | AATATCTGCCTGCCT[A/G]CACCAGACTGCAAAC | 57097 |
rs191766012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3832060 | TAGAAAATAGGAAAG[C/T]TCCCTTTATACAGCA | 57097 |
rs191815255 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3870336 | GGTGGCAAAAGAAGA[A/T]TGTGAGATGATCTGT | 57097 |
rs191978683 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PARP11 | GRCh38.p7 | 12:3845832 | GAGGTCTTTCTCCCC[A/G]AAATACAAGTTTTAG | 57097 |
rs192123722 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3840548 | GCCGGACACCTTCAC[A/G]GATCATAAGAAAACC | 57097 |
rs192153290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3837640 | CGCTTCTCGAATTAA[A/G]GAGCACAGAGTGGCT | 57097 |
rs192171397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3855949 | GACCAATGGAACGGA[A/G]CAGAACAGAGGCCTC | 57097 |
rs192182751 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | PARP11 | GRCh38.p7 | 12:3817873 | TGTCAGAACCCAGAG[C/G]TTCTGATTCAGTAGA | 57097 |
rs192300043 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3852339 | ATAACAAACTTCTCC[C/G]AGCTAAAGGAAGATG | 57097 |
rs192304754 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3818727 | TATTGAAAAATGCAA[A/C]GGAACTTTTCAAATT | 57097 |
rs192306875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3856197 | CCTAGGTAATACCAT[C/T]CAGGACATAGGCATG | 57097 |
rs192307287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3834809 | GAGTCAGAAAGGCAG[C/T]ATAAAAACACTAGGC | 57097 |
rs192310566 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3872848 | CGACAATCGCTTTAA[C/G]CCGGGAGACGGAGGT | 57097 |