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 |