SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs192330865 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3814986 | AATACAAACAATAAG[C/G]CACCATACCAATCTC | 57097 |
rs192455516 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3861083 | CTGCATCTGATTTAG[A/T]TAATATTTAGATGAG | 57097 |
rs192489541 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3820815 | CAGAAATAAAAGTTG[C/G]TTTGGCCAATAGACC | 57097 |
rs192557158 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PARP11 | GRCh38.p7 | 12:3837281 | AGAGCTGAGAAAAAC[A/C]TGAGCGTAAGGCACC | 57097 |
rs192566726 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | PARP11 | GRCh38.p7 | 12:3808816 | AGGTGGAGATGAGAT[A/G]CATAAGTCACAGAAA | 57097 |
rs192703294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3837948 | AAGATCTTAAGTATA[C/T]AAAACAAACATTAAT | 57097 |
rs192706213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3867005 | ATATACAGTATATAA[A/G]GTAAAAGTACTCAAC | 57097 |
rs192750842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3842767 | CTCGTAAAAAGCAGA[C/T]GTTTGTTAAAGTATT | 57097 |
rs192764328 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3813781 | AAAACTTGGATTTTC[A/T]CAACATTATAAATAA | 57097 |
rs192827792 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PARP11 | GRCh38.p7 | 12:3854827 | GCAGAGAAACAACAA[A/C]AAAAAAGAGAATTTT | 57097 |
rs192855083 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3814463 | TGCCCCAATATCATA[A/T]AGGTAATTGATTGTC | 57097 |
rs192892292 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3851056 | ATAATCAAAGATCAT[C/G]ATGAACTGAAAATTG | 57097 |
rs192976652 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3868573 | TAGGCACATTAAACA[C/T]AGTGAGTCCAGAACC | 57097 |
rs192989661 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3817429 | TTGTATCCCCACAGC[A/G]CAGTTTGTTCTAGTG | 57097 |
rs193025932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3842132 | TAAAAGGACCATTCA[A/G]AGTCTGAAAGAAAAA | 57097 |
rs193066432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3834375 | TGGTGGTTCATGCCT[A/G]TGATCCCAGCACTTT | 57097 |
rs193153212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3872259 | TTACACAGTTGTCTA[C/T]TCTTCATGGGTCCTA | 57097 |
rs193187308 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PARP11 | GRCh38.p7 | 12:3847668 | GGATATAGAAGAAAC[A/G]TATCTCAAAATAATA | 57097 |
rs193213638 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3860334 | TCTTCTTTAAGACAA[G/T]GAAGGACCCTAAAAG | 57097 |
rs193214488 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3823097 | ACATGACACACCAAT[C/T]GCCTCCAGTGATTGG | 57097 |
rs199671627 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3830027 | ACATCTCCTGAAAAG[C/T]CAGAAGGAGGTGGAG | 57097 |
rs199747875 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3855691 | ATATCGTGAAAATGG[C/T]CATACTGCCCAAGGT | 57097 |
rs199886851 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PARP11 | GRCh38.p7 | 12:3853024 | CAGAATTTCATATCC[A/C]GCCAAACTAAGCTTC | 57097 |
rs200031294 | snp | A/C/T | 0.00157889 | 0.028053 | intron-variant | PARP11 | GRCh38.p7 | 12:3828868 | TAGATTTTATCATAT[A/C/T]AATATACTAAAAACA | 57097 |
rs200174142 | in-del | -/AGAG | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810701 | AGAAAGAAGGAAGGA[-/AGAG]AGAGAGAAGAGAAGA | 57097 |
rs200198959 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3865889 | ACGTCTTGTTATTTG[A/G]TTTTTTTTTTTTGGT | 57097 |
rs200202111 | in-del | -/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3865476 | TCTCCAGTTAACTGG[-/T]GTATCTTTCTATTTC | 57097 |
rs200259215 | snp | C/T | 1.66432e-05 | 0.00288467 | synonymous-codon, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812144 | AAAGTCTATCAAGTA[C/T]TCAGGATAGATTTGG | 57097 |
rs200269883 | in-del | -/A | 0.00755907 | 0.0610114 | intron-variant | PARP11 | GRCh38.p7 | 12:3862418 | TCACACCACTGCACT[-/A]ACAGCCTAGGCAACC | 57097 |
rs200297732 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3854996 | TGCAAATCAATAAAC[A/G]TAATCCATCACATAA | 57097 |
rs200307166 | in-del | -/AGAGAA/GAGAGA | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810716 | GAGAGAGAGAAGAGA[-/AGAGAA/GAGAGA]AGAGAAAGAGAAAGA | 57097 |
rs200352561 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3833920 | AGGCTGCTGGTGTTT[A/C]TCCTCTCCTTCAGCC | 57097 |
rs200396104 | in-del | -/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3844944 | CCTTCATTTTAACTG[-/T]TTATGTCATACTGTA | 57097 |
rs200456536 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3846777 | AAAAAAAAAAGAAAA[A/G]AAAAAAGAAATAGAA | 57097 |
rs200470341 | in-del | -/T | 0.0197687 | 0.0974348 | intron-variant | PARP11 | GRCh38.p7 | 12:3850644 | ATGTGCATTACTGTG[-/T]TTTTTTTCTTATTCT | 57097 |
rs200502114 | snp | C/G | 0.00299544 | 0.0385843 | intron-variant | PARP11 | GRCh38.p7 | 12:3842414 | AGCCAAGCAGAAGTC[C/G]GGATGAAGGTTATCA | 57097 |
rs200533980 | in-del | -/AAAC | 0.0271762 | 0.113356 | intron-variant | PARP11 | GRCh38.p7 | 12:3866108 | CCCATCATCACTTAA[-/AAAC]AAACAAACAAACAAA | 57097 |
rs200603171 | in-del | -/TC | | | intron-variant | PARP11 | GRCh38.p7 | 12:3824013 | ATTTGAAACAGAATT[-/TC]TGAGTCAAAGAATAT | 57097 |
rs200615337 | snp | C/T | 1.65765e-05 | 0.00287888 | utr-variant-5-prime, missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3830003 | AAAATAATTCTTCTG[C/T]TTTGTGAAACATCTC | 57097 |
rs200836900 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3835373 | TTCAGCTATATCACT[A/G]TTATATACACATAAA | 57097 |
rs200895536 | in-del | -/T | 0.00676609 | 0.0577691 | downstream-variant-500B | PARP11 | GRCh38.p7 | 12:3808613 | TGGCCTGTTTGGGGA[-/T]TTTTTTTTTATAATA | 57097 |
rs200958133 | in-del | -/CAT | 0.0287284 | 0.116357 | cds-indel, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3808948 | CTTTATCATCATCAC[-/CAT]CAACAGTCTAGAAAT | 57097 |
rs200970270 | snp | A/G | | | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839642 | TTTCTCTTATGTACA[A/G]GAAAGATTTTATAAC | 57097 |
rs200998166 | snp | C/T | 0.00199792 | 0.0315431 | intron-variant | PARP11 | GRCh38.p7 | 12:3829065 | GTTTCATTTACCAGC[C/T]GTTCACATTAATGAC | 57097 |
rs201004394 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3853337 | TAAAAGACACAGACT[A/G]GCAAATTGGATAAAG | 57097 |
rs201134354 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3855009 | ACGTAATCCATCACA[C/T]AAACAGAACCAAACA | 57097 |
rs201143468 | in-del | -/GAAGGAAG | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810647 | AGGGAGGGAGGGAAA[-/GAAGGAAG]GAAGGAAGGAAGGAA | 57097 |
rs201236294 | in-del | -/T | | | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3875114 | TTAACAATTTTTTTT[-/T]CAGATCTGCATCAGC | 57097 |
rs201254913 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810650 | GAGGGAGGGAAAGAA[A/G]GAAGGAAGGAAGGAA | 57097 |
rs201392673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3841978 | AAGCCAGACGAAGGC[C/T]GGACAGAGCAATCTT | 57097 |
rs201415742 | snp | A/C | | | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3840402 | GCCAAAGAATCCAAG[A/C]AAGCCAATAAAAGCC | 57097 |
rs201446940 | snp | C/T | 4.94311e-05 | 0.00497123 | intron-variant | PARP11 | GRCh38.p7 | 12:3822073 | GGTATATTCAGTCAA[C/T]TCTGCTCTTACCTGA | 57097 |
rs201472311 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3819489 | GCCAGGAGCACCCCC[A/C]CCCTGCCATATTAAC | 57097 |
rs201575698 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PARP11 | GRCh38.p7 | 12:3861180 | TAATTTGCATGCAAC[A/G]AAGACACAAATTTTT | 57097 |
rs201661286 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3830055 | GAGGAAGAAATAATT[A/C]TATTAATAACAAGTA | 57097 |
rs201709805 | in-del | -/TTTTTATAAACACA | 0.2462 | 0.249971 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3809022 | AGATTTATGAAACTT[-/TTTTTATAAACACA]TTTTTTTTACCCTGA | 57097 |
rs201768174 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3841720 | AATCCATTCTTAGGC[C/G]CAGTTCCTATTGCAC | 57097 |
rs201810855 | snp | C/G/T | 3.29664e-05 | 0.00405984 | missense, synonymous-codon, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3814101 | ATGAATGCAGATTGC[C/G/T]TCCACAAATTCACTG | 57097 |
rs201874770 | snp | C/G | 1.64838e-05 | 0.00287083 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812192 | AAAGATCTTTGGGTT[C/G]CAGGTATCATCCACA | 57097 |
rs201915899 | in-del | -/AA | | | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3875136 | TGCATCAGCATCTGT[-/AA]AAAAAAAAAAAAAAT | 57097 |
rs202030204 | snp | A/C | | | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839114 | ATGCATTAGGCAGGG[A/C]TCCCCTACGCGCCCG | 57097 |
rs202053396 | in-del | -/GGAG | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810622 | AAAAAGAAAAAGGGA[-/GGAG]GGAGGGAGGGAGGGA | 57097 |
rs202057213 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3841659 | TGCTGATTATGAAGA[C/G]TCACTGAGTGGCAAG | 57097 |
rs202084919 | snp | C/G | 0.00299544 | 0.0385843 | intron-variant | PARP11 | GRCh38.p7 | 12:3842555 | TAACAGAAACTCTTA[C/G]GTGGAATGTTTCTGA | 57097 |
rs202091846 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810645 | GGAGGGAGGGAGGGA[A/G]AGAAGGAAGGAAGGA | 57097 |
rs202111420 | snp | A/G | 0.00390459 | 0.0440119 | intron-variant | PARP11 | GRCh38.p7 | 12:3829854 | GATGCTAAGTGAATC[A/G]AAAACACTTCTGCTA | 57097 |
rs202176088 | in-del | -/AGAGA | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810707 | AAGGAAGGAAGAGAG[-/AGAGA]AGAGAAGAGAAAGAG | 57097 |
rs202211855 | in-del | -/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3835379 | TATATCACTGTTATA[-/T]ACACATAAACCAATA | 57097 |
rs202213222 | in-del | -/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3844076 | GATGCCAGCTGGGCT[-/C]AGTGAATCGCCACTG | 57097 |
rs202229764 | in-del | -/AGAC | 0.0283406 | 0.115616 | intron-variant | PARP11 | GRCh38.p7 | 12:3820325 | GGTTATGTGACAGTG[-/AGAC]AGACAAAGTTATTTT | 57097 |
rs207472624 | snp | A/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3823160 | GATCTTTAGTTTACT[A/T]TTTTCAAACTTATTT | 57097 |
rs367581503 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3834077 | TACTCTGGGAGGAAG[C/T]TGGGGCGGTGGCAGT | 57097 |
rs367615737 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3827807 | ACGTTTCACCACCCT[A/C]CCCAGCCACAATACA | 57097 |
rs367663901 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | PARP11 | GRCh38.p7 | 12:3844069 | ATGTTTGGATGCCAG[A/C]TGGGCTCAGTGAATC | 57097 |
rs367788775 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3818009 | GATGCTCTTATTTCC[G/T]TGCTGCCTTATACTT | 57097 |
rs367808606 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3866205 | ATCTTACTTATCTCA[C/T]GGTAACATTTCACAG | 57097 |
rs367840280 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3813771 | CATAAATTGAAAAAC[C/T]TGGATTTTCACAACA | 57097 |
rs367843470 | in-del | -/A | | | intron-variant | PARP11 | GRCh38.p7 | 12:3857637 | GTCCATTATTATGCT[-/A]AAAAAAAAAAAAGGA | 57097 |
rs367871580 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839303 | GCAGGACCAGCAACA[C/T]GGAGGCGGCCGTCGG | 57097 |
rs367973090 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3852981 | GGGGGCCAATATTCA[A/G]CATTCTTAAAGAAAA | 57097 |
rs368023728 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3862665 | TTTTTCTGCATATGG[A/G]TATCCAATTGTTTCA | 57097 |
rs368051783 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3817953 | ATTCTGACCTGCAAC[C/T]AGCTTTGAGAATCTC | 57097 |
rs368053804 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3842104 | GAGAAATTGTGCCTG[C/T]TGAACTTGAACCTAA | 57097 |
rs368136883 | snp | C/T | 6.59337e-05 | 0.0057413 | intron-variant | PARP11 | GRCh38.p7 | 12:3822044 | TACTGCAGTCATTTC[C/T]GGTTTCTTTCATGGG | 57097 |
rs368252702 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3831010 | AAGGAGACAAAGAGG[C/T]TGGTCAAAGAAAATT | 57097 |
rs368301659 | snp | C/T | | | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839294 | TGGCCTGCAGCAGGA[C/T]CAGCAACATGGAGGC | 57097 |
rs368450062 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3834964 | CTGGCCAAACACGAC[A/G]TAACAGAAGCTACTC | 57097 |
rs368460630 | in-del | -/GAG | | | intron-variant | PARP11 | GRCh38.p7 | 12:3822389 | GGATCACGAGGTCAG[-/GAG]ATCGAGACCATCCTG | 57097 |
rs368616546 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3842433 | TGAAGGTTATCAGTA[A/C]CATCGAAATGTCAGA | 57097 |
rs368639636 | snp | C/T | | | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3875189 | TGGGAAGTTTGTTCC[C/T]AGATATTTTATAGTT | 57097 |
rs368644435 | snp | C/T | | | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3870756 | GAAAGATTTAAAACC[C/T]TGAGTAAGACATATA | 57097 |
rs368724568 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PARP11 | GRCh38.p7 | 12:3822553 | GCAGTGAGCCGAGAT[C/T]GCGCCACTGCACTCC | 57097 |
rs368745096 | in-del | -/ATCCCTCTCCTACAA | | | intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3871976 | GTGATAGAAACTAGG[-/ATCCCTCTCCTACAA]AGCAAGCCATAAAAA | 57097 |
rs368746962 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3819284 | ACACAGCAGATACCA[C/T]TTTGGGTCAGGCAAC | 57097 |
rs368758168 | snp | C/G | 3.29576e-05 | 0.00405928 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812208 | CAGGTATCATCCACA[C/G]AGCTGTCATATAAAT | 57097 |
rs368766869 | snp | C/T | 1.65026e-05 | 0.00287246 | synonymous-codon, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812381 | GAATGTGTTCCCATG[C/T]TTTATGTCATCTTTG | 57097 |
rs368807803 | snp | A/G | 3.32303e-05 | 0.00407603 | intron-variant | PARP11 | GRCh38.p7 | 12:3822174 | TTGAAACAGCAAAAG[A/G]GAAAACAAAATATCA | 57097 |
rs368847631 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3821092 | AAATCTTGATAGGTG[C/T]TGAATCAGGATGACG | 57097 |
rs368851956 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3868091 | ATTATCAAATTAGAT[A/G]TAAGTACTTTGTAAG | 57097 |
rs368852660 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3841685 | GCAAGAATATGTTCC[C/T]CCAGCCATCTTTTGG | 57097 |
rs369021894 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3846537 | CAAGGTGGGTGGATC[A/G]TGAGGTCAGGAGATC | 57097 |
rs369092565 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3832548 | TCACAGATGCTCTGG[A/G]TTTCTTTAAAAAGAT | 57097 |
rs369219719 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3867427 | ATGAGATTTTAAAAA[A/G]CAAAAAAATTCTTCA | 57097 |
rs369224208 | snp | A/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3854253 | GAGCAAACAAATTCA[A/T]AAGCTAGCAGAAGGC | 57097 |
rs369268591 | snp | C/T | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3872664 | ACTGATGGCTCCTCT[C/T]AGGCCCATTCAAGAC | 57097 |
rs369310545 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3828406 | ACAAAAAAATTAGCC[A/G]GGTGTGGGGGCGGGT | 57097 |
rs369333986 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3857913 | AATATAAAAATATAT[G/T]CTTGAATAGCATGCT | 57097 |
rs369423151 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3857552 | TGTGCTAATACACAT[A/G]TAAGTGTAAACTTGC | 57097 |
rs369484410 | in-del | -/A | | | intron-variant | PARP11 | GRCh38.p7 | 12:3858463 | AAAGATTTCTAAGAC[-/A]AAAACCATTGTTAAT | 57097 |
rs369576771 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3857069 | CACTCATAAGTGGGA[C/T]TGAACAATGAAAACA | 57097 |
rs369596469 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3833322 | AAAAACTAGTAGGCC[A/G]GGCGTGGTAGCTCAC | 57097 |
rs369641835 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3842936 | ACACTATAGATTCCA[A/G]ACATAACGTTGCACC | 57097 |
rs369670296 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3850848 | TATGGTGTTGAAATG[A/G]CCACTATATATATGA | 57097 |
rs369739123 | snp | G/T | | | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3874906 | GTATACATACACGTA[G/T]ATATCTGTTTCTGAA | 57097 |
rs369760747 | in-del | -/AA | | | intron-variant | PARP11 | GRCh38.p7 | 12:3859560 | GAGTGAGACTCTGCT[-/AA]AAAAAAAAAAAAAAA | 57097 |
rs369896760 | snp | A/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3850150 | CAGTAAATAAGATGG[A/T]ATATGTAATAAATTA | 57097 |
rs369914288 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3853867 | GTACTTATTCCAAAA[C/T]TGACCACATAGTTGG | 57097 |
rs369920477 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3815930 | TACCTGCATTTAAAT[G/T]GTGACAGAGATGAAA | 57097 |
rs369948141 | snp | A/G | 0.000115341 | 0.00759324 | intron-variant, synonymous-codon, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3829019 | AACTGAACACTGACT[A/G]TTGGTATCCGGCTTT | 57097 |
rs369999655 | in-del | -/TT | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3870366 | TGGAGGATTCCCCAC[-/TT]TTAACAAAAGTCAGC | 57097 |
rs370023815 | in-del | -/A | | | intron-variant | PARP11 | GRCh38.p7 | 12:3860423 | TGCTTTCAATAGGCC[-/A]GATGGCTCATGAGGG | 57097 |
rs370053667 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3834551 | AGAGAAGAGAACTGA[C/T]TGAACCCAGGAGGCA | 57097 |
rs370056433 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3861545 | CTTGAGATTTCAGAG[C/T]TCTTAATATATTCTA | 57097 |
rs370120924 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3809557 | GATAAGATCTGCAAA[G/T]TCTAAAAGAAAAACA | 57097 |
rs370593057 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | PARP11 | GRCh38.p7 | 12:3869521 | AGGCTTCTCTCTTTT[A/T]CTCAAGCACCAAGCT | 57097 |
rs370597313 | in-del | -/GACA | | | intron-variant | PARP11 | GRCh38.p7 | 12:3820330 | TGTGACAGTGAGACA[-/GACA]AAGTTATTTTAGTTC | 57097 |
rs370600863 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3856056 | CTATTTAATAAATGG[C/T]GCTGGGAAAACTGGC | 57097 |
rs370674357 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3861450 | ACATCTTTTCATGTT[A/G]TTATTTTCCATCTGC | 57097 |
rs370681676 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | PARP11 | GRCh38.p7 | 12:3822381 | AGGCGAGCGGATCAC[A/G]AGGTCAGGAGATCGA | 57097 |
rs370699241 | snp | A/T | 4.95372e-05 | 0.00497656 | intron-variant | PARP11 | GRCh38.p7 | 12:3829846 | AGCAAGGTGATGCTA[A/T]GTGAATCGAAAACAC | 57097 |
rs370779105 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3865678 | TCACACTTTCTCTTC[A/G]TTAGTGTTAGCACTG | 57097 |
rs370872384 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PARP11 | GRCh38.p7 | 12:3830221 | CTTAACAATTTAGGC[A/G]AGTAATAATAATCTT | 57097 |
rs370886675 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PARP11 | GRCh38.p7 | 12:3843947 | GCCAAAACCAGATGC[A/G]GTGACTTTCTTTTTT | 57097 |
rs370886985 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3844327 | TGTCACCTTCTAAAC[G/T]AGAATAGTTGTTGAA | 57097 |
rs370896677 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3859356 | GATCACAAGGTCAGG[A/G]GATCGAGACCAACTT | 57097 |
rs370908801 | snp | C/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3860294 | CAGGATGGGACCATA[C/G]AGCAATTCAGCTGCA | 57097 |
rs371031802 | snp | G/T | | | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3873559 | AGGAGTTTAAAGGGT[G/T]TCTGGTCCAACTGTA | 57097 |
rs371133153 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3826824 | TAAGTACTTAAAGGT[A/G]TCATTTTCTGCTTTC | 57097 |
rs371141716 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3817007 | CCATCCTAGCTAACA[G/T]GGTGAAACCCTGTCT | 57097 |
rs371221825 | snp | A/C | 1.64953e-05 | 0.00287182 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3821948 | CGATCCATCGTCTTC[A/C]CAAAGAGATTAGCAA | 57097 |
rs371270418 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3837697 | GATCCAAATATATAC[C/T]ACCTACAAGAAACCG | 57097 |
rs371270742 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3818076 | GCCCTTACATTTGTA[C/T]TGCTGAAGTACATTA | 57097 |
rs371309253 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3809474 | TTTCATAGAAACCAA[A/C]TAGGTAAGTTCAGCG | 57097 |
rs371323865 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3814032 | CCTGGAATTCTGATA[A/G]TTACCTTTTCCAAAG | 57097 |
rs371426233 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3825200 | GAAAATAGGAGACAT[A/G]CTTTAAGATTTTTTC | 57097 |
rs371447819 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | PARP11 | GRCh38.p7 | 12:3817959 | ACCTGCAACTAGCTT[G/T]GAGAATCTCTGATCT | 57097 |
rs371474164 | snp | A/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3849714 | TATACAGTTAGATAT[A/T]AGAAATAAGACCTAG | 57097 |
rs371509350 | in-del | -/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3817130 | CGGAGGCGGAACTTG[-/G]CAGTGAGCTGAGATC | 57097 |
rs371527388 | in-del | -/TCA | | | cds-indel, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3808950 | TTATCATCATCACCA[-/TCA]ACAGTCTAGAAATGA | 57097 |
rs371530543 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3841504 | GAGGCTAGTGTTAAT[A/G]GTCAAATGCTACAGC | 57097 |
rs371555081 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3864010 | GAGGTGAGCAAAGGA[A/C]AGTCATGGAAACAAG | 57097 |
rs371680536 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3846420 | AGAAGAAATGGATAA[A/G]TTCCTGGACATATAG | 57097 |
rs371694684 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3868962 | GAGTTTGATTCCCTT[C/T]TAAAGGTTGTATGAG | 57097 |
rs371721460 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3853789 | ACCAAGCAGACCTAA[C/T]AGACATCTACAGAAC | 57097 |
rs371804642 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3860193 | GTATGGATGTGGACC[A/G]CCCCAGCAGGACAAC | 57097 |
rs371982297 | snp | A/G | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3872536 | CCAAGGAAGAAGGCA[A/G]ACTTGCAGTTGAAAT | 57097 |
rs371990290 | in-del | -/A | | | intron-variant | PARP11 | GRCh38.p7 | 12:3868123 | GCTGCAAAAAAAAAA[-/A]TCATCCTTCTCAATG | 57097 |
rs372013391 | snp | A/G | 0.000153988 | 0.00877328 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812115 | ACCACCGAGATTTGG[A/G]AGTGAAATCAATGAA | 57097 |
rs372042761 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PARP11 | GRCh38.p7 | 12:3849533 | AGAATTCGTTATGTC[A/G]AGTAAAATAAGCCAA | 57097 |
rs372072975 | in-del | -/AAAGAG | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810738 | GAGAAAGAGAAAGAG[-/AAAGAG]GAAGAGAAAAAGGAA | 57097 |
rs372123433 | snp | C/T | 0.000140223 | 0.00837209 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812105 | AGCTTCCTTGACCAC[C/T]GAGATTTGGAAGTGA | 57097 |
rs372182498 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3823177 | TTTCAAACTTATTTT[A/G]ATGAAAAAAATCAAA | 57097 |
rs372210257 | snp | C/T | | | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839319 | GGAGGCGGCCGTCGG[C/T]GTCCCCGACGGCGAG | 57097 |
rs372219944 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3819999 | TCCAACTGGTGTCTG[A/G]GGCTCCCTAATTCTA | 57097 |
rs372247839 | snp | C/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3868597 | CAGAACCAAACTCCT[C/G]TTATCTTCCATATGG | 57097 |
rs372254685 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PARP11 | GRCh38.p7 | 12:3844791 | GAATAAAAGAACTGA[C/T]TTTTGATAGTTTTAA | 57097 |
rs372262531 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3826497 | CTGCTCAGTATGCAC[A/G]GTCTATTCCCCTTCT | 57097 |
rs372272808 | snp | C/G | | | intron-variant, splice-acceptor-variant | PARP11 | GRCh38.p7 | 12:3815054 | ACACTTCACCTGTAT[C/G]TGTGTGAAGAGGAAG | 57097 |
rs372310978 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3854198 | GGAAAGATCTAAAAT[C/T]GACACCCTAACATCA | 57097 |
rs372314497 | snp | C/T | 3.39357e-05 | 0.00411906 | intron-variant | PARP11 | GRCh38.p7 | 12:3822201 | ATCAGAAGCCGATTA[C/T]AATTACTGTCAAGAA | 57097 |
rs372332103 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3815787 | ATAAACTGAATGCAA[C/T]AGATTTCAGTTAAGC | 57097 |
rs372375954 | snp | C/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3835901 | ATTAGAGAAATGTGG[C/G]ATACCATTAAGTGCA | 57097 |
rs372428384 | snp | A/G/T | 3.29527e-05 | 0.00405898 | missense, synonymous-codon, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812237 | ATTCACATAGCTCCC[A/G/T]TCTTTGGAAGGAGGT | 57097 |
rs372488017 | snp | A/G | 0.000386317 | 0.0138928 | intron-variant | PARP11 | GRCh38.p7 | 12:3812478 | AGCCAAGATTACTCC[A/G]AAGAATATATTAAAA | 57097 |
rs372499819 | snp | C/T | 0.000181394 | 0.00952177 | intron-variant | PARP11 | GRCh38.p7 | 12:3822013 | AATAAGCTGGAAAAA[C/T]AAATTTGCATAGATT | 57097 |
rs372510878 | snp | C/T | 1.71431e-05 | 0.00292767 | intron-variant | PARP11 | GRCh38.p7 | 12:3826266 | ATATTAGATAAGTCA[C/T]AAAAGTACACTGTAC | 57097 |
rs372511638 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3863735 | TATGTGTGACAATAT[A/G]TGCAAAGTGTTACCA | 57097 |
rs372512750 | in-del | -/A | 0.431916 | 0.171483 | intron-variant | PARP11 | GRCh38.p7 | 12:3822443 | CTCTACTAAAAATAC[-/A]AAAAAATTAGCCAGG | 57097 |
rs372516551 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3854503 | TCAGAGAATACTATG[A/G]ACACCTCTACGCAAA | 57097 |
rs372682362 | snp | A/G | 1.71929e-05 | 0.00293192 | intron-variant | PARP11 | GRCh38.p7 | 12:3814206 | AAAAACACAATATAC[A/G]CAGACACAAAAGCAC | 57097 |
rs372733167 | snp | C/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3831616 | GACCTCAATGAAGGG[C/G]GTTTGTTATTTTTTA | 57097 |
rs372876081 | snp | C/T | | | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3871540 | GTACACTCTATGACG[C/T]TGGCACAATGAAAAA | 57097 |
rs372876996 | snp | C/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3866052 | CTATGCTAACACCCA[C/G]TCCAATTTAACTTTT | 57097 |
rs372942382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3851632 | TGGGTGGAGCCCACC[A/G]CAACTCAATGAGGCC | 57097 |
rs372958750 | snp | A/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3834223 | CCAGGAGCAGTGGCA[A/T]GGAGACTTTGCTCAG | 57097 |
rs372962478 | in-del | -/GTGCC | | | intron-variant | PARP11 | GRCh38.p7 | 12:3812949 | TTACAGGCGCGTGCC[-/GTGCC]ACCACACCCAACTAA | 57097 |
rs372993181 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3863410 | ATAAAGAATGGACAT[A/C]ATTGCCTTGTTCTTG | 57097 |
rs373021693 | snp | A/G | | | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3840143 | ATTCCATTGCTGCTG[A/G]CTTACAATATGAAGT | 57097 |
rs373053480 | snp | A/G | 3.35396e-05 | 0.00409496 | intron-variant | PARP11 | GRCh38.p7 | 12:3828874 | TTATCATATCAATAT[A/G]CTAAAAACACACAAC | 57097 |
rs373054564 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3846856 | TTGGGAGGCTGAGGT[A/G]GGAGGATCATTTATG | 57097 |
rs373298041 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3809558 | ATAAGATCTGCAAAG[G/T]CTAAAAGAAAAACAA | 57097 |
rs373453922 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3847218 | CTCAGGACCTGATGG[C/T]TTCACTGCTGAATTC | 57097 |
rs373477334 | snp | C/G | 0.000181253 | 0.00951808 | intron-variant, synonymous-codon, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3829022 | TGAACACTGACTGTT[C/G]GTATCCGGCTTTAAG | 57097 |
rs373508149 | snp | A/T | 1.64963e-05 | 0.00287192 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3821952 | CCATCGTCTTCCCAA[A/T]GAGATTAGCAACTTC | 57097 |
rs373515221 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3823788 | AGGCATGGTGGCGTG[C/T]GGCTGTAATCTCAGC | 57097 |
rs373641739 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3863487 | AAAGGCATTCTGAAG[A/C]TGCCCTTTGTGTCAG | 57097 |
rs373688184 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PARP11 | GRCh38.p7 | 12:3837449 | TGCAAAAACCTATAA[C/T]AGACCCACTAAAAAT | 57097 |
rs373730442 | snp | C/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3834615 | CTCCAGCCTGGGCGA[C/G]AAGAGCGACACTCCA | 57097 |
rs373757204 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PARP11 | GRCh38.p7 | 12:3861606 | TTAAATACTTTCTCC[C/T]GTCTGTGGCTTATCT | 57097 |
rs373964504 | snp | A/G | | | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3874078 | TCCATGCAACAAAGG[A/G]TCTACCCCATAGGAA | 57097 |
rs374123803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3861286 | CTAACTCCTAATGTG[A/G]TATGAAAATGGGGCC | 57097 |
rs374272850 | snp | A/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3817056 | ATTAGCCAGGCGTGG[A/T]GGCGGGCGCCTGTAG | 57097 |
rs374295478 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PARP11 | GRCh38.p7 | 12:3852805 | AGATACTCCTTGAGA[C/T]GAGCAACCCCAAGAT | 57097 |
rs374337187 | in-del | -/GAA | | | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3840707 | AGAATGGATACAGAA[-/GAA]CGAAAAGACAAAGAC | 57097 |
rs374462037 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PARP11 | GRCh38.p7 | 12:3864148 | ATTTTAATCAGGAAT[C/T]GATATTCGATTTTGT | 57097 |
rs374469926 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3845007 | CAAAAGTATAGAACT[G/T]AGGATCATTTGCATT | 57097 |
rs374484346 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3870228 | ATTTTTAAAACCAAA[C/T]TGCGCTTACTGATAT | 57097 |
rs374487198 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3860080 | ACCAGTACTTAAAGA[G/T]GCAGAAAATTCTCAA | 57097 |
rs374572150 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3836093 | TATAGATATAAATCT[A/G]CACATCCAAGAAGCT | 57097 |
rs374584617 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3812831 | TTTTTGAGACAGAGT[A/C]TTGCTCTGTCTCCCA | 57097 |
rs374584749 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3850517 | TATATTTTCCTCACA[C/T]GTCCAGATTCCCCCA | 57097 |
rs374674534 | snp | A/G | 0.000167272 | 0.00914373 | intron-variant | PARP11 | GRCh38.p7 | 12:3822189 | AGAAAACAAAATATC[A/G]GAAGCCGATTACAAT | 57097 |
rs374848058 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3858104 | CAATTGGTGATTTCG[A/C]AGGACTCTGTATATC | 57097 |
rs374874015 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3816186 | TTTATAAAAACAAAC[A/G]AAAAAAGTTTTTTAA | 57097 |
rs374885323 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3828200 | AAAAGTTGTTCTTGA[A/G]ACTATTGCCAGCTAC | 57097 |
rs374892752 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3843069 | AAGGCCTTTCATCTC[A/G]ATATCTGTCAAACTT | 57097 |
rs374976574 | snp | A/G | 6.59348e-05 | 0.00574135 | intron-variant, missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3828948 | AATTTGGAAGTAGTA[A/G]AAGAAATGGAGCCAC | 57097 |
rs375117870 | snp | A/C | | | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3869999 | ATGATTCGTGGCCCC[A/C]GGCAGGATGGAGCAC | 57097 |
rs375129663 | snp | A/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3842746 | TTTATCTATCAAGTG[A/T]CTGTCCTCGTAAAAA | 57097 |
rs375141699 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3826835 | AGGTATCATTTTCTG[A/C]TTTCATCCATGCCTC | 57097 |
rs375152906 | snp | A/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3855749 | CAAGCTACCAATGAC[A/T]TTCTTCACAGAATTG | 57097 |
rs375159867 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810273 | AAAGGCTTGGTATAC[A/G]TGCTGTCTTTTAAAG | 57097 |
rs375257620 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PARP11 | GRCh38.p7 | 12:3823826 | GAGGCTGAGACAGGA[G/T]AATCACTTGAACCTG | 57097 |
rs375268862 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3857139 | TCGGGGGGTGGGGGG[A/C]TGGGGGAAGGATAGC | 57097 |
rs375362108 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3835923 | TTAAGTGCACCAACA[C/T]ATAAATAACTACAGT | 57097 |
rs375478849 | snp | C/G | | | downstream-variant-500B | PARP11 | GRCh38.p7 | 12:3808761 | ACAAACTCCTTGGGT[C/G]CACTAAGATTGAGCT | 57097 |
rs375495258 | snp | A/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3848807 | ATGGATCACTGGAAT[A/T]ACATCAAACTAAAAA | 57097 |
rs375575295 | snp | A/G | 4.94303e-05 | 0.00497119 | stop-gained, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812254 | CTTTGGAAGGAGGTC[A/G]CATGTATTTGGAGTC | 57097 |
rs375633595 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3819686 | ACTGTCCCAGGAAAA[A/C]ATCCAAACCTCTTAG | 57097 |
rs375644866 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3829729 | TGGGGAAAAGAAAAG[G/T]AAAAGCACTGGAAGA | 57097 |
rs375662067 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3825271 | GTCTTCTGACATTTA[C/G/T]ACCTCCTTTTTCAGA | 57097 |
rs375665436 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3844084 | CTGGGCTCAGTGAAT[C/T]GCCACTGTACTGTAA | 57097 |
rs375731617 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3813101 | TGAGCCACCATGCCC[A/G]GCCCTGAGTTTTACT | 57097 |
rs375770108 | snp | A/C | | | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839895 | AGCTGATGAAGACAA[A/C]AGTGAAATATCAGAT | 57097 |
rs375797208 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3832277 | AATTACACTATTTTT[G/T]TCGTCCACAATCCAA | 57097 |
rs375822519 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3837897 | GGTCAACGAAGCAAG[C/T]GGACATAATTATAAA | 57097 |
rs375927875 | snp | A/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3850416 | ACTCCTGACTTCATG[A/T]GATGGGTCACAGTCA | 57097 |
rs375960264 | snp | C/T | 1.6483e-05 | 0.00287076 | splice-donor-variant | PARP11 | GRCh38.p7 | 12:3829889 | AAAGGAAAGGAGGTA[C/T]CTGAAACATGTGCCA | 57097 |
rs376005332 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PARP11 | GRCh38.p7 | 12:3867965 | TAAACATCTGACAGC[A/G]CCAGCAAACACAAGT | 57097 |
rs376105042 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3852240 | TCTCCTCCAAAGGAA[C/T]GCAGCTCCTTGCAAG | 57097 |
rs376136897 | snp | C/T | 6.59326e-05 | 0.00574125 | intron-variant, synonymous-codon, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3829028 | CTGACTGTTGGTATC[C/T]GGCTTTAAGACAAAC | 57097 |
rs376223375 | snp | C/T | 0.000307953 | 0.0124049 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3821967 | AGAGATTAGCAACTT[C/T]ATTATATTCATGTGT | 57097 |
rs376259044 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3847447 | AAAACTGAATTCAAC[A/G]ACACATTAAAAAAAT | 57097 |
rs376297972 | in-del | -/CAAA | | | intron-variant | PARP11 | GRCh38.p7 | 12:3866123 | AAACAAACAAACAAA[-/CAAA]AGACACTTCCTAGGA | 57097 |
rs376342419 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3813127 | TTACTGCTTGGCCCT[C/G]CCTCCCGTTTCTATT | 57097 |
rs376364846 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | PARP11 | GRCh38.p7 | 12:3863639 | AAACGCACATGGGGT[A/G]AAGTCTAGAAGAAAC | 57097 |
rs376376094 | snp | C/T | 0.000118802 | 0.00770629 | intron-variant | PARP11 | GRCh38.p7 | 12:3826247 | TTCTGTATACAAAGA[C/T]AAGATATTAGATAAG | 57097 |
rs376396521 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3857252 | TGTACGTTGTGCACA[C/T]GTACCCTGGAACTTA | 57097 |
rs376430479 | snp | A/C | 1.64836e-05 | 0.0028708 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812355 | TGTTGCAAGCTGACA[A/C]CATGAATTTGGAATG | 57097 |
rs376474725 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3853612 | TATATGCACCCAATA[C/T]AGGAGCACCCAGATT | 57097 |
rs376516977 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3814573 | GAATTCCTTGAGCAG[A/G]GATCATGTCATATGC | 57097 |
rs376594663 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3818027 | CTGCCTTATACTTCC[C/T]AGCTCTGGATCAATC | 57097 |
rs376602843 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3867418 | AAATGAGGGATGAGA[A/T]TTTAAAAAACAAAAA | 57097 |
rs376626775 | snp | C/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3831836 | AAACTGTCCAGTAAA[C/G]TATTCACAATTCCTA | 57097 |
rs376661315 | snp | C/T | | | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3869880 | GGACTTCGCACTAAC[C/T]AGCTTATAACAGGTG | 57097 |
rs376679674 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3850091 | AAGCTATATTGGAGA[A/C]GGAAATAACACCATA | 57097 |
rs376688161 | snp | A/G | 1.74653e-05 | 0.00295505 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812106 | GCTTCCTTGACCACC[A/G]AGATTTGGAAGTGAA | 57097 |
rs376733857 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3841692 | TATGTTCCCCCAGCC[A/G]TCTTTTGGACCCAAT | 57097 |
rs376791349 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3821088 | TGGTAAATCTTGATA[A/G]GTGTTGAATCAGGAT | 57097 |
rs376791586 | snp | A/G/T | 0.000891607 | 0.0210981 | intron-variant | PARP11 | GRCh38.p7 | 12:3826267 | TATTAGATAAGTCAT[A/G/T]AAAGTACACTGTACT | 57097 |
rs376847006 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3842020 | AAGGCAGATATGGCA[C/T]TGGCTTCCATCCCTC | 57097 |
rs376858480 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3841454 | AGAATTAAAGTGATT[A/G]TACCTGTACTGATGC | 57097 |
rs376872039 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3868703 | TCTCCTCTCTCCCCA[C/T]TTAGTAGTCACCTTC | 57097 |
rs377080565 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3843511 | ACTTTCACTTTACAC[G/T]TGCATGTTCTCCTTG | 57097 |
rs377082516 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3812728 | CTGTTTTTAAAATAA[A/G]TCTTACAAAGAAAAC | 57097 |
rs377110665 | snp | A/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3830556 | TATCTGTGTAAGTGT[A/T]TGTAAATGTTTACAC | 57097 |
rs377153218 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3809592 | CCAAATGCTGTAACA[A/G]TTTTTCCATTCAAGT | 57097 |
rs377163954 | snp | A/G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3866731 | CAAGAGAAAAGACGC[A/G/T]TTCCTCAGCTAAAAC | 57097 |
rs377170190 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3861010 | AGCACATATTTGGTT[G/T]CACAGGGTCACAGCT | 57097 |
rs377283605 | snp | A/C | 0.000875616 | 0.0209055 | intron-variant | PARP11 | GRCh38.p7 | 12:3826099 | AGTCTATTTGTTTTT[A/C]TGTCCAATAGTAAGA | 57097 |
rs377332040 | in-del | -/GAGAA | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810718 | AGAGAGAGAAGAGAA[-/GAGAA]AGAGAAAGAGAAAGA | 57097 |
rs377399949 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3815947 | TGACAGAGATGAAAA[C/T]GCATACGGTCTTTCT | 57097 |
rs377410833 | snp | A/C/T | 1.64817e-05 | 0.00287064 | intron-variant | PARP11 | GRCh38.p7 | 12:3822055 | TTTCCGGTTTCTTTC[A/C/T]TGGGTATATTCAGTC | 57097 |
rs377427205 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3825855 | ACTCAGCCTCCCGAG[C/T]AGCTGGGACCACAGG | 57097 |
rs377464920 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3816098 | TTACAAAAAGTCAGC[A/G]TGCTTTCACTAAGAA | 57097 |
rs377472481 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3858413 | AGTGTGCATTCATAC[C/T]AAACAAGAATTCATG | 57097 |
rs377486588 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3844297 | TTTTGAGAGAATCTA[C/T]TGAAAGGAATTTGTT | 57097 |
rs377497123 | snp | A/G | 4.9489e-05 | 0.00497414 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3821934 | CATAGATTTACTGC[A/G] | 57097 |
rs377529594 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3864153 | AATCAGGAATCGATA[C/T]TCGATTTTGTCAAAG | 57097 |
rs377539571 | snp | A/G | | | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3874056 | AGCTAACAGAGTGAA[A/G]TAATCTTCCATGCAA | 57097 |
rs377635540 | snp | A/C/T | 8.25449e-05 | 0.0064239 | intron-variant | PARP11 | GRCh38.p7 | 12:3829853 | TGATGCTAAGTGAAT[A/C/T]GAAAACACTTCTGCT | 57097 |
rs377684940 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3861373 | TCTTAATATTTGCCA[A/G]TCTGATAGATGGGCA | 57097 |
rs377686035 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3826975 | TCAAAATGATTATGT[G/T]TACCCACCCAGGCTA | 57097 |
rs377699563 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3837688 | AAAAACCAAGATCCA[A/G]ATATATACTACCTAC | 57097 |
rs377702641 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3815611 | TGAAATAGCAACAGT[A/C]CAGATATCATCAGAC | 57097 |
rs377705240 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3832718 | GGCTCTAGGCTAGGA[C/T]ACATTTATAGGTAAT | 57097 |
rs377734469 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3851858 | GAGACACCTCCCAGT[A/C]GGGGCCGACTGACAC | 57097 |
rs386375431 | in-del | -/AAAGAG | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810733 | AGAAAGAGAAAGAGA[-/AAAGAG]AAGAGGAAGAGAAAA | 57097 |
rs386759720 | in-del | ATTAGCCAGGCGTGGG/TTAGCCGGGCGTGGT | | | intron-variant | PARP11 | GRCh38.p7 | 12:3822449 | TAAAAATACAAAAAA[lengthTooLong]GGCGGGCGCCTGTAG | 57097 |
rs386759721 | in-del | AA/GTTATAT | | | intron-variant | PARP11 | GRCh38.p7 | 12:3835373 | TTCAGCTATATCACT[AA/GTTATAT]ACACATAAACCAATA | 57097 |
rs386759722 | multinucleotide-polymorphism | GTC/TTT | | | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3841016 | CTGCTCCAATTCCTG[GTC/TTT]GGTCAGTGACACAGA | 57097 |
rs397776871 | in-del | -/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3865901 | TGCTTTTTTTTTTTT[-/T]GGTCCCACCTGTTCT | 57097 |
rs397818975 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812007 | GGAGGCCACTTTTTT[-/T]CATATCTGTTTCAAA | 57097 |
rs397840476 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3842860 | ACACATTTCCAACAT[C/T]TGAAATCAGACTTAT | 57097 |
rs397849999 | in-del | -/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3809030 | TGAAACTTTTTTTTT[-/T]ACCCTGAGGCTGATA | 57097 |
rs397850387 | in-del | -/A | | | intron-variant | PARP11 | GRCh38.p7 | 12:3837677 | GAAGAAAAAAAAAAA[-/A]CCAAGATCCAAATAT | 57097 |
rs397850714 | in-del | -/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3823513 | TAGTACACACTCAGT[-/T]AAGTACTGGATGAAT | 57097 |
rs397850943 | in-del | -/A | | | intron-variant | PARP11 | GRCh38.p7 | 12:3816211 | TTTTAAATTAAAAAA[-/A]GAAGATAATACTTGT | 57097 |
rs397850984 | in-del | -/AA | | | intron-variant | PARP11 | GRCh38.p7 | 12:3817203 | TCAAAAAAAAAAAAA[-/AA]TTCATTTATCACTAC | 57097 |
rs398018247 | in-del | -/T | 0 | 0 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3875151 | TGCAAACCTATGTGA[-/T]TTTTTTTTTTTTTTT | 57097 |
rs398076380 | in-del | -/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3866663 | ACTTTCAGATTATTT[-/T]TCACACAAAGCACAA | 57097 |
rs398116032 | in-del | -/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3822740 | TGTCTTGTTTTTTTT[-/T]GAAATTTCCAAAATT | 57097 |
rs527263354 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3817402 | GAGGGCAGGGGCATG[A/G]TGGTTAAAGCTTTGT | 57097 |
rs527284686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3828268 | AGTAAAAAAGTTCTG[A/G]CCAGGCAAGGTGGCT | 57097 |
rs527316166 | snp | C/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3852454 | TTAAATGACCTGATG[C/G]AGCTGAAAACCATGG | 57097 |
rs527451144 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3813808 | ATAACGTGAAGTTTT[C/T]CCCCACTATTCCTTA | 57097 |
rs527514261 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3821757 | GACCAGGTCAAAATA[C/T]GGCAAGAGAAAAACA | 57097 |
rs527526296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3861903 | GGTGGAGGGTGCCTA[C/T]AGTCCCAGCTACTCG | 57097 |
rs527557440 | snp | C/G | | | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3874478 | TGGCCAGGCCAGTCT[C/G]GAACTCCTGACCCCA | 57097 |
rs527580729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3861379 | TATTTGCCAATCTGA[C/T]AGATGGGCAGTATTG | 57097 |
rs527615698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3820974 | ACAAAAGTCAGCCTA[A/G]TTCTCAGGTATATAG | 57097 |
rs527672838 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3811426 | AGTGTAGGCTAATGA[C/T]ATTTTGCAGCAATTA | 57097 |
rs527679288 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3820028 | TACCCACTCCACTCC[A/G]CATCCCCTACTTTTG | 57097 |
rs527721586 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3859669 | AGATTTTTCAGATTA[G/T]ATTTTTTTGAAATCC | 57097 |
rs527732837 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3852027 | GCAAACTCCAACAGA[C/T]GTGCAGCAGAGGAAC | 57097 |
rs527781947 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3867709 | TGATTACACTATTGT[A/G]TGTATAAAGAACATG | 57097 |
rs527795715 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3825493 | TTACGGCCCCAGTAA[C/T]TGTATGGCTCTGAGA | 57097 |
rs527800589 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3874311 | TCGCCCAGGCTGGAG[C/T]GCAGTGGCGCCATTT | 57097 |
rs527868545 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3840996 | TTTTGGACCAACAGG[G/T]GTCCCTGCTCCAATT | 57097 |
rs527992413 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PARP11 | GRCh38.p7 | 12:3817117 | AATGGCATGAACCCC[A/G]GAGGCGGAACTTGCA | 57097 |
rs528016068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3853049 | AGCTTCATAAGTGAA[A/G]GAGAAATAAAATCCT | 57097 |
rs528044369 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PARP11 | GRCh38.p7 | 12:3816834 | TTGAATCCAGGAGGC[A/G]GAGGTTGTAATGAGC | 57097 |
rs528121612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3864504 | ATTTCTTCCTTAAAT[A/G]TTTGGTAGAATTCAC | 57097 |
rs528134684 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3862699 | TCATTAGTTAAAACA[A/G]CTGTCCTTTTCCCAC | 57097 |
rs528161255 | in-del | -/TA | 0.00199481 | 0.0315187 | intron-variant | PARP11 | GRCh38.p7 | 12:3862604 | GTATATTTTATATAC[-/TA]TATATATAATTTTTA | 57097 |
rs528228967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3823144 | TAATAAATTTCAAAC[C/T]GATCTTTAGTTTACT | 57097 |
rs528271667 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PARP11 | GRCh38.p7 | 12:3844879 | GTATTAATTAGTCCA[C/G]GGGATTTTGCCTTAT | 57097 |
rs528292714 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3861207 | TTTTCGTGGAGGGAA[A/G]GGCCAGGGCCAGAAT | 57097 |
rs528309437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3823643 | AAAGCTGGCTGGGCG[C/T]GGTGGCTCATGCCTA | 57097 |
rs528351856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3851300 | CAAGCCGAAGAAGGG[C/T]AGGGCATCGCCTCAC | 57097 |
rs528415676 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3850696 | CTGTTGACAAGGTCA[C/G]AAAGGCCTGCAGATA | 57097 |
rs528457321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3842479 | GGAGATAGGAGGAGA[C/T]CAGGGATGGGAGATG | 57097 |
rs528522242 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3849295 | ATTATCCAGCAACTC[C/T]ACGACTGAGTATATA | 57097 |
rs528528083 | snp | A/G | | | intron-variant, nc-transcript-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3871705 | CTGCCACCTTACCAG[A/G]CAGTTTCAACCATAA | 57097 |
rs528625931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3866341 | ACTTCTCCTCAGCTT[A/G]TAACTTTTAGAGTTT | 57097 |
rs528654237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3871620 | GCACGACTGTATTTA[A/G]TCCAACAACTTGCTG | 57097 |
rs528687731 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3841537 | GTGATTGGACCGCCG[A/C]CATTTTCTTCACCTC | 57097 |
rs528689578 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3869890 | CTAACTAGCTTATAA[C/T]AGGTGCTCAATAAAT | 57097 |
rs528693713 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3830932 | CAATTAACTCACATA[C/G/T]GCATTATCTTTGAAA | 57097 |
rs528693742 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PARP11 | GRCh38.p7 | 12:3822516 | AGGCAGGAGAATGGC[A/G]TGAACCCGGGAGGCG | 57097 |
rs528740988 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3860978 | CCACCAAACTCAGAC[A/C]ACCATTGCATTTTGG | 57097 |
rs528867432 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3840226 | GACGTTCAAGGAGTT[C/G]ATTCTGAGAATGGAC | 57097 |
rs528901416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3846550 | TCGTGAGGTCAGGAG[A/G]TCGAGACCATCCTGG | 57097 |
rs528913716 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3845973 | TTTGTGTATGAAAAA[C/T]GATAATAGCCTTACA | 57097 |
rs528913803 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3852793 | AGAACACCACAAAGA[G/T]ACTCCTTGAGACGAG | 57097 |
rs528929565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839682 | ACCTAATGTTTCTCC[C/T]TCACAAGTAACTGAA | 57097 |
rs528976217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3852195 | AACCAGAGCAGAAAA[A/G]CTGAAAATTCTAAAA | 57097 |
rs529002775 | in-del | -/AT | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3829107 | GGTGGTACTGTGGTC[-/AT]AGAGACAGGGAATGG | 57097 |
rs529012576 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3874902 | ATAGGTATACATACA[C/G]GTATATATCTGTTTC | 57097 |
rs529089922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3834503 | GCCAGGTGTGGTGGC[A/G]TGCACCTGTAGTTCC | 57097 |
rs529094069 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | PARP11 | GRCh38.p7 | 12:3852658 | AAATCTATGTTTGAT[A/T]GGTGTACCTGAAAGT | 57097 |
rs529098099 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3819516 | TAACAATCAAAAATG[A/T]CTCCAGTCATTACCA | 57097 |
rs529158758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3854736 | TTCCTTCTGAAACTA[C/T]TCCAATCAACAGAAA | 57097 |
rs529260693 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3873301 | GGGTGTTGGATTTTT[C/T]TTTTTCCCGCGGGTC | 57097 |
rs529261338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3832355 | AACCGAAGCAGAGAA[C/T]AATACAATTTTTTGT | 57097 |
rs529321891 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3831981 | GGAAGAATGAGATTG[A/G]AGCTAATAGTTAAGA | 57097 |
rs529362470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3838990 | CCTGAGTCGGGCAGC[A/G]AGGCCGTCGGGAAGT | 57097 |
rs529442847 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810447 | ATACAAAAATTAGCC[A/G]GGCATGGTGGTATGC | 57097 |
rs529494973 | in-del | -/A | 0.00517822 | 0.0506191 | intron-variant | PARP11 | GRCh38.p7 | 12:3812825 | CTGTTTTTTTGAGAC[-/A]AGAGTCTTGCTCTGT | 57097 |
rs529510644 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3818253 | TATCAACACCTCCCT[A/T]CACTTCATTCGCTGT | 57097 |
rs529523663 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3859095 | AGAGCAAGACTCCAT[A/C]TCAAAAAAAAAAAAA | 57097 |
rs529556313 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3858608 | CAAAAAATACAGTGT[A/G]TAGGAGCATTTTAAT | 57097 |
rs529567969 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3865446 | TCCATCAATTATTTG[C/G]AGAAAACTACTGAAA | 57097 |
rs529640543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3821776 | AAGAGAAAAACAGCA[C/T]GTCTACACCACTGAA | 57097 |
rs529667772 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3858980 | TAGGCGCCTGTAATC[C/G]CAGTTACTTGGGAGG | 57097 |
rs529668927 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3829130 | AGGGAATGGAGGGGC[A/G]AGGGAAACTTACTAA | 57097 |
rs529680612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3870434 | TTCAAAGAAAACCCA[C/T]TGCTTACAAAGAAAT | 57097 |
rs529714485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3828373 | TCAACATGATGAAAC[A/G]CTGTCTCTACTAAAA | 57097 |
rs529718061 | snp | C/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3824917 | TCCACAGAAGTACTA[C/G]AGCATTCATTTTATA | 57097 |
rs529742446 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3814930 | TCAAAATAATACTGT[A/G]TATTATGTAGGTATA | 57097 |
rs529876249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3856104 | ATCCCTTCCTTACAC[C/T]TTATATAAAAATTAA | 57097 |
rs529973300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3822384 | CGAGCGGATCACGAG[A/G]TCAGGAGATCGAGAC | 57097 |
rs529994873 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3855526 | AACTCCCATTCACAA[C/T]TGCTACAAAGAGAAT | 57097 |
rs530020924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3871404 | TGTTTAGATACATAA[A/G]TACTTTCCATTGTGT | 57097 |
rs530032618 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3874309 | TGTCGCCCAGGCTGG[A/G]GCGCAGTGGCGCCAT | 57097 |
rs530096049 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3846948 | AAATTAGCTGGGCAC[A/G]TGCCTGTGGTCCCAA | 57097 |
rs530122146 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812084 | CCTTCCTGCAAAAAA[G/T]AATAAAGCTTCCTTG | 57097 |
rs530139358 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3868645 | ATTCCTGGCTGCCCA[C/T]GCCAGAAAGCTAAGT | 57097 |
rs530146927 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3853926 | AGAACAGAAATCATA[A/C]CAAACTGTCTCTCAG | 57097 |
rs530236378 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3849519 | ACATGGATGAAATGA[A/G]AATTCGTTATGTCAA | 57097 |
rs530253786 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3820185 | CCCAGAACAGTGCTT[A/G]TCATAAAGTAGGTAC | 57097 |
rs530370607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3848366 | AAAGCAATCTTGAGC[A/G]AAAATAAGGCTAGAG | 57097 |
rs530433252 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3847371 | GACACAACAAACAAA[C/G]AAAACCATAGGCCAA | 57097 |
rs530476298 | snp | A/G | 0.00478085 | 0.0486577 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3809765 | TTGTTTTTTGTGAAC[A/G]GGTTTAGAGCCATGG | 57097 |
rs530514033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3857453 | CTGTTTTGACATTAT[C/T]ATCCTAGAAAGACAC | 57097 |
rs530545518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3817236 | TTCGGGCACAAATTC[A/G]ATTGAATCTCGGTTT | 57097 |
rs530593910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3832499 | GTTATTTCTCCTCTC[C/T]TATGTTGCTAACATT | 57097 |
rs530765265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839134 | CTACGCGCCCGGAGA[A/G]CGCGGACCGCTGCCT | 57097 |
rs530781636 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PARP11 | GRCh38.p7 | 12:3844955 | ACTGTTTATGTCATA[C/G]TGTATGTTGACATAT | 57097 |
rs530788470 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3837425 | TTGTAAGTCTTGCGG[C/T]AACCATAATGCAAAA | 57097 |
rs530853309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3843288 | AAATATCATGGTGCC[C/T]ACTCGAAAGAAATGT | 57097 |
rs530865536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3842521 | CAGCACGCTTGACGG[C/T]TGTTGCCGAAGTATT | 57097 |
rs530893200 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3854855 | TTTAGACCAATATCC[C/T]TGATGAACATCAACG | 57097 |
rs530929219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3849768 | TAGATCAGTAGGGTG[A/G]CTGTAGTTTACAATA | 57097 |
rs530973623 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3836674 | GCTGGCTTTGCTCCC[C/T]GCCCCCACAGAAAAC | 57097 |
rs530974507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | PARP11 | GRCh38.p7 | 12:3863850 | CCTGTTACTGAAGCT[C/T]CAGATTCCCAGAGGG | 57097 |
rs531075487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3831139 | AAAATCAGAACTTTC[A/G]AAATAAAGCTAAAGA | 57097 |
rs531127102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3823813 | CTCAGCTACTCGGGA[A/G]GCTGAGACAGGAGAA | 57097 |
rs531127129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3816006 | ATTTAAATGTATATG[C/T]TTTGATCTATTTGTG | 57097 |
rs531127135 | in-del | -/AATTGGGATTA | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3845796 | ATTTACTCTCCCACT[-/AATTGGGATTA]TTTTTTAAAAGAGGT | 57097 |
rs531127354 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3823313 | GTAATTAGTTTCTTG[G/T]GTATTCTTCCAGAGC | 57097 |
rs531136718 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3831776 | CACTATTTACCTTAT[A/T]TATTTTAACCACATA | 57097 |
rs531243941 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3840969 | GCCAGCCTGGCCAAG[G/T]GAACCTACAACTTTT | 57097 |
rs531318398 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PARP11 | GRCh38.p7 | 12:3846629 | AGGTGTGGTGGCAGG[C/T]GCCTGTAGTCCCAGC | 57097 |
rs531324131 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3853759 | AGGATATCCAGGACT[G/T]GCACTCAGCTCTGCA | 57097 |
rs531366109 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3869587 | TGCTGTCTGAACAGC[C/T]CTCCCCACCTTCCAG | 57097 |
rs531395374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3820904 | AAAACCTGAAATGTA[C/T]GCAGGCCATATTAAC | 57097 |
rs531466509 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3850476 | CAAGGGAAAAAAGAC[C/T]TTCCCAGGCCCTTTC | 57097 |
rs531478262 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3868821 | ACAGCCCCTTATCCC[C/T]CTCAGTATTTTCTTT | 57097 |
rs531537829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3820215 | CTAAGACATTTTTGT[C/T]AGAAGAAGTGGGGAA | 57097 |
rs531567299 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3874238 | CTATCCTTCCATTCC[A/G]TTAAGTTTAAATCTG | 57097 |
rs531586183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3818445 | ACCACACTTCTTCAG[A/G]AGCTAGAATCCATCA | 57097 |
rs531588015 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | PARP11 | GRCh38.p7 | 12:3825893 | ACCACATCCAGCTAA[-/T]TTTTTTTTGTATTTT | 57097 |
rs531596519 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3826696 | AACTCACAGAATTTC[A/C]AAAATTTCTACATTT | 57097 |
rs531598890 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3827595 | AAATCCTGCTTATTT[C/G]CCTAATGGCATTAAA | 57097 |
rs531646824 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3828693 | TAAGACAATCTTCAC[A/G]TACATTAATATATAC | 57097 |
rs531731435 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3825976 | ACTCGTGATCAGGCC[A/G]CCTCGGCCTCCCAAA | 57097 |
rs531796770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3833112 | CTGATATAAATTTTA[A/G]TTTACTACAACAAAG | 57097 |
rs531899362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3852294 | AATGACTTTGACGAG[C/T]TGACAGAAGTTGGCT | 57097 |
rs531908385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3819082 | ACTGCTGTATATCAA[C/T]TAATACTCCCTTTCC | 57097 |
rs531959917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3852936 | TAACAGTGGATCTCT[C/T]GGCAGAAACTCTACA | 57097 |
rs531977603 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3814956 | GTATACATACACAGG[C/T]AGTAAAAAATACAAA | 57097 |
rs532022757 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3818787 | ATCGTACAGATGGCA[A/C]CTACTTGTGTAAACC | 57097 |
rs532031927 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3859579 | AAAAAAAAAAAAAAG[A/G]CAGATGTAAATAATA | 57097 |
rs532045986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3867543 | AATAGCGTGAACCTA[C/T]TACTTCAGGGCCAAA | 57097 |
rs532046029 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3809202 | AATGGTTGTGTCCAG[C/T]ATTATTATATACTGG | 57097 |
rs532075796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3830175 | TCATATTGGCTCTGA[A/G]GATAAACATTAAAAA | 57097 |
rs532095858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3871893 | CTCTGATCTCCTGCC[C/T]TTCTGTCTCCTGCCC | 57097 |
rs532107543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3871561 | CAATGAAAAAAATCA[C/T]CCAGCAATGAACTTC | 57097 |
rs532199762 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3861055 | CTCAGGATGAATCAT[A/G]CCTTGGGCTCAACTG | 57097 |
rs532363119 | in-del | -/GATAAAATGAATGTAAT | 0.00159617 | 0.0282053 | intron-variant | PARP11 | GRCh38.p7 | 12:3861152 | CTCTGGGGTGATTGG[-/GATAAAATGAATGTAAT]TTGCATGCAACGAAG | 57097 |
rs532448807 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3863644 | CACATGGGGTGAAGT[A/C]TAGAAGAAACCACAT | 57097 |
rs532459999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3861851 | AACACGGTGAAACCC[C/T]GTCTCTACCAAAAAT | 57097 |
rs532469718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3861300 | GATATGAAAATGGGG[C/T]CTTTGGGAGGTGATT | 57097 |
rs532472130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3856152 | AGACTTAAATGTTAG[A/G]CCTAAAACCATAAAA | 57097 |
rs532526748 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3844266 | TAAAGACTGGGATGG[C/T]TGTGTGGAAAACATT | 57097 |
rs532661345 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3867459 | AATGCTGACAATACC[A/G]AAAAGTAATTCTATG | 57097 |
rs532688976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3813071 | CGACCTCCCAAACTG[C/T]TGGGATTACAGGCGT | 57097 |
rs532717692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3829231 | TCTCCAGTGAAGAGA[C/T]AACTGGTTATAGTCC | 57097 |
rs532741620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3815929 | ATACCTGCATTTAAA[C/T]GGTGACAGAGATGAA | 57097 |
rs532796872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3842381 | AACATGTGAGAAGTG[A/G]GGAGTCCTGGAAAGG | 57097 |
rs532796882 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3836072 | ACACACATATATATG[C/T]GTGTGTATAGATATA | 57097 |
rs532805048 | in-del | -/ATT | | | intron-variant | PARP11 | GRCh38.p7 | 12:3817983 | CTGATCTAAATTCAC[-/ATT]ATTAACAAGATGCTC | 57097 |
rs532809040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3842002 | CAATCTTCCCAGACA[C/T]GAAAGGCAGATATGG | 57097 |
rs532826075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3859066 | TCATGTCATTGCACT[C/T]GAGCCTGGGCGACAG | 57097 |
rs532836177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3845038 | TTTGAGTTGGAAATT[A/G]TGAAACTTCACCATA | 57097 |
rs532977063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3826032 | CTGCGCCTGGCCCAA[A/G]ATTTGATATTTAAAA | 57097 |
rs532978726 | snp | C/T | 0.00478085 | 0.0486577 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810401 | TTGAGATCAGCCTGG[C/T]CAACATGACAAAACC | 57097 |
rs533089991 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3855217 | ATTCCCTTTGAAAAC[C/T]GGCACAACACAGGGA | 57097 |
rs533093887 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3809858 | AGATGCTTTTTAAAG[A/C]GCTTTTTCTAAATAT | 57097 |
rs533137884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3831875 | TTTTATTAATGTTCA[C/T]TTCATTGGGCCATTT | 57097 |
rs533139763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3833756 | AGTCAGAGTCTGTGG[C/T]GTTTGAGTTACAAAC | 57097 |
rs533154416 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3857143 | GGGGTGGGGGGCTGG[A/G]GGAAGGATAGCATTA | 57097 |
rs533168905 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3833124 | TTAGTTTACTACAAC[A/C]AAGTATAATTTATTT | 57097 |
rs533195366 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3838390 | AAGGAAATTTAAAAT[A/C]TCTTAAAGCAAATGA | 57097 |
rs533234234 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839539 | AACAGAGAGAAATTT[C/G]AAGCGATTATAGGAG | 57097 |
rs533282172 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3843318 | TAGATGCTACGCATT[C/T]TGAAAATAATCTGCA | 57097 |
rs533385610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3865376 | CAAGCAGATCAAGTT[A/G]GTTGACAGTGGTGTT | 57097 |
rs533388236 | in-del | -/TATC | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3842733 | CATTCAGAATCTGTT[-/TATC]TATCAAGTGACTGTC | 57097 |
rs533414527 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3832273 | ATCAAATTACACTAT[A/T]TTTTTCGTCCACAAT | 57097 |
rs533483288 | in-del | -/ATTA | 0.00199481 | 0.0315187 | intron-variant | PARP11 | GRCh38.p7 | 12:3862776 | ATTCTATTCCATTCC[-/ATTA]ATTAACTTCCCTAAC | 57097 |
rs533549214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3820278 | TGCTGGATGGACTCA[C/T]GTGGGCCTGACTACC | 57097 |
rs533552044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3827709 | TGGGATAATAATTAT[C/T]GCATATTTGGTTCCA | 57097 |
rs533614625 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3827100 | CAGCATGTGGAGCAA[C/G]ACCTGTGATGCCATC | 57097 |
rs533638825 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3861346 | AGTCCTCATAAATGG[C/T]ATTAAGGCTTTTCTT | 57097 |
rs533745656 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | PARP11, LOC105369609 | GRCh38.p7 | 12:3872441 | AGTTTTCGGCCCCTA[C/T]GTTGCACTTTAAATA | 57097 |
rs533775103 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PARP11 | GRCh38.p7 | 12:3811753 | CTGTATTTTTTTTCA[A/G]CATTTATACGAATAA | 57097 |
rs533791982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3819787 | TCAACTAAGGCTACT[A/G]AAGACGATCACACAA | 57097 |
rs533829107 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3854125 | AGAATCTCTGGGACA[C/G]ATTTAAAGTAGTGTG | 57097 |
rs533950061 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810759 | GAAAAAGGAAGAGAG[A/G]GAAAGAGGAAGAGGA | 57097 |
rs533982513 | in-del | -/C | 0.00478085 | 0.0486577 | intron-variant | PARP11 | GRCh38.p7 | 12:3869017 | AGCTTCTAGAAGCTA[-/C]CCACATACCTTGGCT | 57097 |
rs534024198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3847589 | ATATAATCATTTTAA[C/T]AGATGCTTTAAAAGC | 57097 |
rs534042734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3866795 | TCAATTCAAATTTAA[C/T]GCCTGAGAAGAAACA | 57097 |
rs534109334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3834070 | GGCCCTGACTGCCAC[C/T]GCCCCAACTTCCTCC | 57097 |
rs534189415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3846669 | GGCTGAATCAGGAAA[A/G]TGGCGTGAACCCAGG | 57097 |
rs534222253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3852338 | AATAACAAACTTCTC[C/T]GAGCTAAAGGAAGAT | 57097 |
rs534283488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3851957 | TCTGCAATATTTGCT[A/G]TTCTGCAGCCTCCGC | 57097 |
rs534283631 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PARP11 | GRCh38.p7 | 12:3859285 | AAATGGCAGATGTAG[C/G]CCGGTGCAGTGGCTC | 57097 |
rs534296062 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3858730 | TGCACTGCTTAGTTA[A/T]CCTGAACACATTATT | 57097 |
rs534461217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839965 | GCTGCTGATGTGAAT[A/G]GATTTAAACCTTTGT | 57097 |
rs534532870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3846159 | CCTGTTTATTTTTCT[A/G]TGTTCTGTTTTGTAG | 57097 |
rs534704611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3849535 | AATTCGTTATGTCAA[A/G]TAAAATAAGCCAAGC | 57097 |
rs534745457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3815130 | TGGGAGTCTGCAAAC[C/T]ATTTGCTGCATTTTC | 57097 |
rs534770290 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3841726 | TTCTTAGGCCCAGTT[C/T]CTATTGCACCTCCTT | 57097 |
rs534826270 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3848655 | CACATTAAAAAATCA[A/C]ATCAAAATGAATTAA | 57097 |
rs534876735 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3862273 | GCCTGGGGAACATAG[A/C]AAAACCCCATCTCTA | 57097 |
rs534895061 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810139 | TGAGCAATATAAGCA[C/T]AGACACTGGAATTTT | 57097 |
rs534896868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3814365 | ATGTTCTTGGACACA[C/T]AAATCATCTCATCAA | 57097 |
rs534906312 | snp | A/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3826817 | AAGAGACTAAGTACT[A/T]AAAGGTATCATTTTC | 57097 |
rs534914792 | snp | C/T | 1.64969e-05 | 0.00287196 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3822153 | CCTCGTTTTCACAGA[C/T]GTAACTTGAAACAGC | 57097 |
rs534999702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3836231 | AACAACTGATCACAT[A/G]TAAGAGAATCCTAAT | 57097 |
rs535055029 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3873407 | TACAGACCACCCAAC[C/T]TCCCGACTTCCGCCC | 57097 |
rs535088484 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3836564 | TGGTAAAAGGTATAA[C/T]TGCTGATTTCTCCTT | 57097 |
rs535143033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3841283 | TTCGATTCTTCTTCA[A/G]TCTTGGTGTGAAGGC | 57097 |
rs535151836 | snp | G/T | | | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839409 | ACTGGGCTTGTATCG[G/T]AAACTGGTCGCCAAG | 57097 |
rs535202933 | in-del | -/TGT | 0.00478085 | 0.0486577 | intron-variant | PARP11 | GRCh38.p7 | 12:3823400 | TACATTTATTGCACC[-/TGT]TTTTTTGGTTTTTAC | 57097 |
rs535215016 | snp | A/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3828227 | CTACCTATGACTTTC[A/T]CACTTAACATCTGTT | 57097 |
rs535346898 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3827142 | TCTCATTTTTTAGTT[C/T]ACTTTTCACCATTTT | 57097 |
rs535371142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3870201 | CTAGAGAAACCCACA[C/T]GTAGAATGTTGATTT | 57097 |
rs535393128 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3873872 | AGATTTTATAATCTA[A/G]AAAAGAAAGCAAAAA | 57097 |
rs535429281 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | PARP11 | GRCh38.p7 | 12:3825720 | GATTTGATATTTTTT[A/T]AATTAATTAGTTTAT | 57097 |
rs535482314 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3832657 | CTCAAAGAGTTAAGT[A/C]AAATTTAAATTAATA | 57097 |
rs535483492 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3816234 | ATACTTGTTTTTACC[C/T]ACTGTTTCAATCTTC | 57097 |
rs535492906 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839343 | CGGCGAGGACCAGGG[C/T]GGCGCGGGGCCCCGC | 57097 |
rs535528194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3823499 | ACAGAGCCTGGCACA[C/T]AGTACACACTCAGTA | 57097 |
rs535716834 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3856108 | CTTCCTTACACCTTA[C/T]ATAAAAATTAATTTT | 57097 |
rs535718803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3866998 | TTGACACATATACAG[C/T]ATATAAGGTAAAAGT | 57097 |
rs535721255 | snp | A/G | 3.45907e-05 | 0.00415862 | intron-variant | PARP11 | GRCh38.p7 | 12:3826278 | TCATAAAAGTACACT[A/G]TACTATAAAGTGTCA | 57097 |
rs535831626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3817052 | AAAAATTAGCCAGGC[A/G]TGGTGGCGGGCGCCT | 57097 |
rs535857415 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3821017 | TTATGGTCTGGGATT[G/T]GCTTAAAAATACTTC | 57097 |
rs535907471 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3820328 | TATGTGACAGTGAGA[C/G]AGACAAAGTTATTTT | 57097 |
rs535947476 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3872650 | AAGGGAAAAGGAGAA[C/G]TGATGGCTCCTCTTA | 57097 |
rs536061174 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3849487 | TAAAAAAGAATGGAG[C/T]CATGACATTGGCAGC | 57097 |
rs536071340 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3849322 | TATACCTAAAAGAAA[A/C]AAAATCAGTACACTG | 57097 |
rs536151107 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PARP11 | GRCh38.p7 | 12:3857675 | AGGCATGTATCACCA[A/G]AAACCTCTTTTCTGA | 57097 |
rs536161534 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3854671 | CCAAAAAAAGTCCAG[C/G]ACCAGACAGTCCTGA | 57097 |
rs536173387 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3808906 | TGTAAAAGCAATACA[C/T]TCATATATCAAAATT | 57097 |
rs536174915 | snp | A/G | | | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3871364 | CCAAAGATTGTTAAC[A/G]CTTTATTTTACTGTA | 57097 |
rs536208627 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3854165 | ATTTACAGCACTAAA[G/T]GCCCACAAGAGAAAG | 57097 |
rs536249559 | snp | C/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3814296 | GTAAAACAGGAAATA[C/G]TTTAATATAAATAAC | 57097 |
rs536256958 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3812549 | TTGTATAATAAAAAT[A/C]GATGTGGAATTTCCT | 57097 |
rs536321062 | snp | C/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3836922 | AAAAGTGAGATTAAG[C/G]TGGCCAACCAGCTTT | 57097 |
rs536331647 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3869837 | AAGGCTGGAGCCTAG[A/T]CTGTTCTGTTCACCA | 57097 |
rs536392675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3869195 | TCTCTTTATCTTAAG[A/G]TCAGCTGATTAGCTA | 57097 |
rs536532621 | in-del | -/TCAGGCCGCC | 0.00398564 | 0.0444627 | intron-variant | PARP11 | GRCh38.p7 | 12:3825969 | TCTCCTGACTCGTGA[-/TCAGGCCGCC]TCGGCCTCCCAAAGT | 57097 |
rs536633752 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3859652 | TAATCCAATCAAAAC[A/G]TAGATTTTTCAGATT | 57097 |
rs536636056 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3871348 | GCATATACAAGTGGT[C/T]CCAAAGATTGTTAAC | 57097 |
rs536707821 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3816063 | ACATCAGAAGGTCGT[A/G]CATTTAGCAAATGTT | 57097 |
rs536735063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3853201 | AACTGTAAAGACCAT[C/T]GATGCTAGGAAGAAA | 57097 |
rs536887217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3823558 | TATTTTACAGACGCA[C/T]AGAACTCCGCCATGT | 57097 |
rs536903411 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PARP11 | GRCh38.p7 | 12:3831513 | CACAAAATGAAAAAT[A/G]ATAGACTCCTTCCTC | 57097 |
rs536966451 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3840571 | AGAAAACCTGATCGT[C/G]AAAGAGTTGAGGATT | 57097 |
rs537055512 | in-del | -/AT | | | intron-variant | PARP11 | GRCh38.p7 | 12:3848163 | AAAGAAATTAAAGAC[-/AT]AAAAATGGAAAGATA | 57097 |
rs537136504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3842981 | ATTTTATTATGCAAT[A/G]CCTTAGTCATAAACT | 57097 |
rs537150590 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3856922 | AGAAAATGTGGCACA[C/T]ATACACCACGGAATA | 57097 |
rs537184669 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3861559 | GTTCTTAATATATTC[G/T]ATGTACAAGTCATTT | 57097 |
rs537211256 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | PARP11 | GRCh38.p7 | 12:3856352 | ACAGAATGGGAAAAA[A/T]TTTTTGCAATCTACC | 57097 |
rs537217784 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3872733 | TGGCAGGTAAACCTG[A/C]GGCAAATGACTGACT | 57097 |
rs537292983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3838590 | CAAAATTAACAGAAG[A/G]AAATAATAAATACCA | 57097 |
rs537325870 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3863031 | TTTCGACTTATTTAG[G/T]TCTTAATTTTTTCAA | 57097 |
rs537394477 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3874504 | CCCCAGGTGATCCAC[C/G]TGCCTTGGCCTCCCA | 57097 |
rs537422289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3867158 | AGAGCATGAAGTATA[C/T]AAATAGCAAAAACAT | 57097 |
rs537427856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3830362 | ATGTATTTGGTCAAA[A/G]GGACCCATGCTATCA | 57097 |
rs537485722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3833988 | GAGGACCCGTCTCTC[C/T]TTCCCTACACAGCCC | 57097 |
rs537578964 | in-del | -/TT | | | intron-variant | PARP11 | GRCh38.p7 | 12:3845541 | ATTTATTTTGGCCTC[-/TT]TTGTTTTACCCTTCA | 57097 |
rs537687857 | in-del | -/T | 0.0126979 | 0.078662 | intron-variant | PARP11 | GRCh38.p7 | 12:3831855 | CACAATTCCTACTGC[-/T]TTTTTTTTATTAATG | 57097 |
rs537703490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3822575 | CTGCACTCCAGCCTG[A/G]GCGACAGGGCGAGAC | 57097 |
rs537747285 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3859985 | AATTTGCTGAAGGAG[G/T]GGCCTGGGTCCTCCT | 57097 |
rs537761336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3868098 | AATTAGATATAAGTA[C/T]TTTGTAAGAAGCTGC | 57097 |
rs537771603 | in-del | -/GTCCCTGGTAT | | | intron-variant | PARP11 | GRCh38.p7 | 12:3823255 | TTTCCTCCCACTCCA[-/GTCCCTGGTAT]GTCCCTGGTATGTCC | 57097 |
rs537786645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3862389 | CCAGGAGTTCAATGT[C/T]ACAATGAGCTATGAT | 57097 |
rs537860505 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3809211 | GTCCAGTATTATTAT[A/G]TACTGGTTATATAAT | 57097 |
rs537902950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3833325 | AACTAGTAGGCCGGG[C/T]GTGGTAGCTCACACC | 57097 |
rs537921804 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3817108 | AGGCAGGAGAATGGC[A/C]TGAACCCCGGAGGCG | 57097 |
rs537928710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3857816 | CCCATAAAAAATAAT[A/G]TTTATAACATGTACT | 57097 |
rs537935574 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3873950 | GTGAATAGAGAGTGC[C/T]ATGCGAGCATATTTA | 57097 |
rs538035117 | snp | A/G | 6.59076e-05 | 0.00574016 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812218 | CCACACAGCTGTCAT[A/G]TAAATTCACATAGCT | 57097 |
rs538047204 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PARP11 | GRCh38.p7 | 12:3811670 | AGCAACAGATGGATT[A/G]GTGGATGATACTACT | 57097 |
rs538074482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3846065 | AAAAAAGTATATATA[C/T]GTATCTTTTGAAGTG | 57097 |
rs538078352 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839362 | GCGGGGCCCCGCGAG[A/G]ACGCGACGCCCATGG | 57097 |
rs538110371 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810952 | CAACATGCCCGCCAA[G/T]TTGCTGTCTCGCCTC | 57097 |
rs538138234 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3845382 | CAGACTGTATTCTTG[C/G]AGTGTGTTGTTTCCT | 57097 |
rs538202429 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3858697 | TAACATCTGATAAAG[G/T]TATTTTGGTGATGCT | 57097 |
rs538255285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3814287 | ATAGAAAGCGTAAAA[C/T]AGGAAATACTTTAAT | 57097 |
rs538318129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3865816 | TCTCTGTATTTTAAT[C/T]GGGGTGTTTGATCCA | 57097 |
rs538379425 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3864905 | GTAGTGATTTCCACT[A/C]TAACCTTTATTTCCT | 57097 |
rs538504164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3842186 | GACTGCTGCTGATGT[A/G]GTCAGCCCTGGGGCC | 57097 |
rs538533670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3851901 | GATGCCCCTCTGAGA[C/T]GAAGCTTCCTGAGGA | 57097 |
rs538579390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3849479 | TCGAGCTGTAAAAAA[A/G]AATGGAGTCATGACA | 57097 |
rs538592713 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3863817 | GTCATGTAAACATAA[C/T]AGCACCTGTGTGACT | 57097 |
rs538724630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3854797 | AGGCCAGCATCACCC[C/T]GATACCAAAGCCTGG | 57097 |
rs538737911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3862152 | ATTTTTCTCAGCCAG[A/G]CATAGTGGCTCATCC | 57097 |
rs538748163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3847520 | GGATGGTTCAACATA[C/T]GCAAATCAATCAACA | 57097 |
rs538838475 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PARP11 | GRCh38.p7 | 12:3821397 | ATTTCCCACTTAAAT[C/T]CAGTAAGGAATTGAG | 57097 |
rs538905371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3828420 | CGGGTGTGGGGGCGG[A/G]TGCCTGTAATCCCAG | 57097 |
rs539024304 | snp | A/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3866733 | AGAGAAAAGACGCAT[A/T]CCTCAGCTAAAACAG | 57097 |
rs539028245 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | PARP11 | GRCh38.p7 | 12:3834355 | CAAAAACAGTGGGCC[A/G]GGTGTGGTGGTTCAT | 57097 |
rs539179471 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3843799 | AACTGTAGCTTATAT[G/T]CCTTATTTGTACATA | 57097 |
rs539209155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3870124 | ACCGCAGCTGACTTC[C/T]GGTAAGTGAAATTGT | 57097 |
rs539276619 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3827809 | GTTTCACCACCCTAC[C/T]CAGCCACAATACACT | 57097 |
rs539292591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3835416 | CAAACAACCACAATA[A/G]GGATCAGTATCCAGA | 57097 |
rs539325095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3869292 | AGGAGGCCATTATTA[C/T]GTCTACCATATTTTC | 57097 |
rs539380560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3872793 | GAAAGCAAAACACAA[A/G]GTTTCAAAAAACAGT | 57097 |
rs539423004 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839289 | GCGCCTGGCCTGCAG[C/G]AGGACCAGCAACATG | 57097 |
rs539441162 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3851129 | AGAAAAGATACAGCA[C/T]TGGGGGTCCATTCCA | 57097 |
rs539454797 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3872589 | GAACGAAAACATCTA[A/T]GAACATACAGTCCAT | 57097 |
rs539480251 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3844358 | GGTACCGCTTAAGCC[A/G]TTTCTTTCTTAACAC | 57097 |
rs539485690 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PARP11 | GRCh38.p7 | 12:3838719 | TTAGTCTTAGCAAGG[A/C]TAAGAAAAAAAGAGA | 57097 |
rs539504355 | snp | A/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3853048 | AAGCTTCATAAGTGA[A/T]GGAGAAATAAAATCC | 57097 |
rs539504392 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3823986 | TCCACTTGTTTATCT[A/G]TAAAATAACATATTT | 57097 |
rs539517790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3830476 | GAGTGTAAAAGATTA[C/T]AAAAAAATAGAAATA | 57097 |
rs539535493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3871764 | TCCCACTCTCTGAGG[A/G]TTGTGTTGGGGCTCA | 57097 |
rs539614932 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3817769 | AAGAATACTTTCATG[C/T]TCTGGATTAAAATAA | 57097 |
rs539633959 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PARP11 | GRCh38.p7 | 12:3836066 | ACACTCACACACATA[C/T]ATATGTGTGTGTATA | 57097 |
rs539709762 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3833249 | AAGCTTAAAAATGAA[C/T]GAGAACTTCCAGAAT | 57097 |
rs539710704 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3873369 | GGCCTTCCTCCTCCC[C/T]CTCCCTGTCACAAGC | 57097 |
rs539715690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3832578 | TGCATTTTATAAGAT[C/T]AAACATTTCCATTTT | 57097 |
rs539742481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3857021 | TTCTGAGCAAACTAT[C/T]GCAAGGACAGAAAAC | 57097 |
rs539773788 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3872153 | GAAATGATACACAGA[C/G]AGGCCAAGAAGAATC | 57097 |
rs539824406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3815258 | AGTGTCAAGTACTCA[C/T]AGCATCACGTGCTCA | 57097 |
rs539962296 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3856255 | AAAGCAGTGGCAACA[A/T]AAGCCAAAATAGACA | 57097 |
rs540031404 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3840797 | CTGATGATAAATATG[A/C]AACAGTTTCATCACC | 57097 |
rs540078253 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3833739 | TACTCAATCTCAGAA[A/C]AAGTCAGAGTCTGTG | 57097 |
rs540094938 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3816070 | AAGGTCGTGCATTTA[A/G]CAAATGTTTACTTTA | 57097 |
rs540145944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3853596 | CTAACTATCCTAAAT[A/G]TATATGCACCCAATA | 57097 |
rs540166044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3814672 | ACATTAAGCCATCCA[A/G]TTTAATCCTCTTCCC | 57097 |
rs540267737 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3838972 | GCGACCCCCGGCCTG[A/G]GTCCTGAGTCGGGCA | 57097 |
rs540295253 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810405 | GATCAGCCTGGCCAA[C/T]ATGACAAAACCCCGC | 57097 |
rs540410995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3826391 | CTTTACCATGCAGCT[A/G]GCTATGTACCACGTT | 57097 |
rs540441195 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3874085 | AACAAAGGATCTACC[C/T]CATAGGAAATGAAAA | 57097 |
rs540483584 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3814454 | CCCATGCTATGCCCC[A/G]ATATCATAAAGGTAA | 57097 |
rs540518368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3840069 | CAATCCTGCAGTCTA[C/T]AGAAATGTGGAATAT | 57097 |
rs540594263 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839378 | ACGCGACGCCCATGG[A/G]CGCCTATCTGCGGAA | 57097 |
rs540697684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3835948 | TACAGTATCAGAAGC[A/G]GAGGAGAGAGAAAAA | 57097 |
rs540716961 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3844800 | AACTGACTTTTGATA[C/G]TTTTAAAATTAATCT | 57097 |
rs540759938 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PARP11 | GRCh38.p7 | 12:3841922 | TTCCAGCAGCCAGGA[G/T]TGAACATGTACATTC | 57097 |
rs540776169 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3866387 | TAGCCCTTCTTGTTT[A/T]CTCTCAGAATCTTCA | 57097 |
rs540806458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3818141 | TAGCTAAGCCCTCAA[C/T]GCTGACAGAAATCCT | 57097 |
rs540827239 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3873498 | GCTTATCCATACGCG[A/C]GCGGGCGGTCGTCCT | 57097 |
rs540843977 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3814677 | AAGCCATCCAGTTTA[A/G]TCCTCTTCCCAAGGA | 57097 |
rs540869964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3825919 | ATTTTTAGTAGAGAC[A/G]GGGATTCACCGTGTG | 57097 |
rs540877105 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3822380 | GAGGCGAGCGGATCA[C/T]GAGGTCAGGAGATCG | 57097 |
rs540884768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3871359 | TGGTCCCAAAGATTG[C/T]TAACACTTTATTTTA | 57097 |
rs540889186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3829794 | TTCCTTAAGCTTTGA[C/T]TTCAAGTTCTATATT | 57097 |
rs541131219 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PARP11 | GRCh38.p7 | 12:3848973 | AAAGAAAAAAAAAAA[A/C]ACAAATAATCCAATT | 57097 |
rs541313782 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3857100 | CCTGGACACAGGGCA[A/G]GGAACATCACACACC | 57097 |
rs541327647 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3812884 | CTCAGCTCACTGCAA[A/C]CTCCGCCTCCCAGGT | 57097 |
rs541379514 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3859436 | GGCGTGGTGGCACAC[A/G]CCTGTAGTCCCAGCT | 57097 |
rs541403675 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PARP11 | GRCh38.p7 | 12:3861150 | GACTCTGGGGTGATT[C/G]GGATAAAATGAATGT | 57097 |
rs541476858 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PARP11 | GRCh38.p7 | 12:3864564 | TTTTAGAATGATTTT[C/T]TTCTGCAAATTCAAA | 57097 |
rs541483878 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3827930 | AAGAAAGCCTCCCAT[C/G]CAGGTCTTGTTTGCC | 57097 |
rs541500064 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PARP11 | GRCh38.p7 | 12:3834928 | GAAACTTCATTGGCA[C/T]AAGGGTCTGAATCAC | 57097 |
rs541572019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | PARP11, LOC105369609 | GRCh38.p7 | 12:3872480 | TATAAAAGCAAAGTA[A/G]ACAAAGACACATGAA | 57097 |
rs541606136 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3854834 | AACAACAAAAAAAAA[A/G]AGAATTTTAGACCAA | 57097 |
rs541615715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3813466 | AGACATCATTAAGGG[C/T]ATTCTTACTCTAAAA | 57097 |
rs541659500 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810298 | TTAAAGGCAGAATCA[C/T]AGAAAATCAGGCCGG | 57097 |
rs541725179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3854318 | GATAGAGGCACAAAA[A/G]ACTCTTCAAAAAAAC | 57097 |
rs541737959 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3858774 | AAATGTATGTCATAC[C/T]TTTTACTGTTAAGAA | 57097 |
rs541789660 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3850531 | ATGTCCAGATTCCCC[C/G]ACGCAAGCATGTCCA | 57097 |
rs541874281 | snp | C/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3817105 | CTGAGGCAGGAGAAT[C/G]GCATGAACCCCGGAG | 57097 |
rs541884981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3824838 | AAGTAATTCTTTTAT[C/T]ATATTATTTGTACTA | 57097 |
rs541897006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3823789 | GGCATGGTGGCGTGC[A/G]GCTGTAATCTCAGCT | 57097 |
rs541960226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3831707 | TAAATTTGGTTGGCT[C/T]CTAAGAAATGAAAAA | 57097 |
rs541980764 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | PARP11 | GRCh38.p7 | 12:3860178 | CATTTGATAAGATTA[G/T]TATGGATGTGGACCG | 57097 |
rs542013474 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3852023 | TCCAGCAAACTCCAA[A/C]AGACGTGCAGCAGAG | 57097 |
rs542120893 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PARP11 | GRCh38.p7 | 12:3851080 | AAAATTGAAAAGAAT[A/C]CTGAATACTCAACAG | 57097 |
rs542146027 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3858102 | AACAATTGGTGATTT[C/T]GAAGGACTCTGTATA | 57097 |
rs542179574 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PARP11 | GRCh38.p7 | 12:3847040 | TATGACTGCACCACT[A/G]CACTCCAGCCTGGTC | 57097 |
rs542273479 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3815465 | CCTACCTAGGCTTTC[A/T]TTTCTTGGTTAAATA | 57097 |
rs542293775 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3860571 | ATTTCATGGAACTTG[C/T]TCGGGACCTGTCACC | 57097 |
rs542331465 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PARP11 | GRCh38.p7 | 12:3811799 | AATCATTTATCCTGA[C/T]AACACACACGTAAAC | 57097 |
rs542359208 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3862627 | TAATTTTTATAGTAT[A/G]GCAAAGTATGGAGTG | 57097 |
rs542412898 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3825254 | AATAATAAATATGTA[C/T]TGTCTTCTGACATTT | 57097 |
rs542437226 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3838108 | ACATACTAGATCAAA[C/T]AGGCCTGTCATTTAC | 57097 |
rs542482816 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3835028 | AAATGAAACAGCACT[C/G]TCATCCCTGACAGTC | 57097 |
rs542506315 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3841355 | CTCTGCACCAGGCCT[A/C]CCTGGCAGCCTGCAG | 57097 |
rs542514228 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3847855 | AATAAATGGCAACCA[A/C]ATTGGAGAGAAAGAA | 57097 |
rs542518623 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3840850 | TGCCCTTCTCCTGCA[C/G]AACAAAAGCCAGCAG | 57097 |
rs542529768 | in-del | -/G | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3808892 | CTTTAATCATCACAT[-/G]TAAAAGCAATACATT | 57097 |
rs542817821 | snp | C/T | | | downstream-variant-500B | PARP11 | GRCh38.p7 | 12:3808425 | TTGCCAAAGGTTGAA[C/T]GGAATGTTTAACTCA | 57097 |
rs542899860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3834508 | GTGTGGTGGCGTGCA[C/T]CTGTAGTTCCAGCTA | 57097 |
rs542963762 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3833537 | TGAGCCTAGGAGTTT[G/T]AGGCTGCAGTGAGCT | 57097 |
rs543029558 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3873546 | CTGTGTCTGACGAAG[A/G]AGTTTAAAGGGTTTC | 57097 |
rs543096063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839418 | GTATCGGAAACTGGT[C/T]GCCAAGGACGGGTCG | 57097 |
rs543096700 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3812879 | GCGATCTCAGCTCAC[C/T]GCAACCTCCGCCTCC | 57097 |
rs543241542 | in-del | -/A | 0.41408 | 0.188621 | intron-variant | PARP11 | GRCh38.p7 | 12:3828545 | ACAGTGAGACGTCTC[-/A]AAAAAAAAAAAAAAA | 57097 |
rs543266930 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3822959 | CTCTCCAACAGTCCA[C/G]TACCTTTAAGGGTTA | 57097 |
rs543391660 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3874187 | ATACCTATAGATTTA[C/G]AACCTGATTTTTTTT | 57097 |
rs543402886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3861815 | GGATCACGAGGTCAG[A/G]AGATTGAGACCATCC | 57097 |
rs543404073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3871470 | TGTACAGATTTCTAG[A/G]TTAAGAGCAATAGGC | 57097 |
rs543425753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3870258 | TCATTCATATGCTTA[C/T]AGGAAGAAAAACTAT | 57097 |
rs543437032 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3837017 | GTACCTGAAGGGAGA[A/C]CTATCCCTGAAAACA | 57097 |
rs543522838 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3832034 | TATCTTTTCTCTATT[A/G]GAAAAGAGAATAGAA | 57097 |
rs543547938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3842360 | ATTCTGGTAGGGGCG[A/G]ATATCAACATGTGAG | 57097 |
rs543593143 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3864243 | TGAATTACATTGATG[A/G]CTGTTCAAATATTAA | 57097 |
rs543675324 | in-del | -/AAGTGAGATT | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3836909 | TTTCTACACTGGAAA[-/AAGTGAGATT]AAGGTGGCCAACCAG | 57097 |
rs543717609 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3830800 | GGCATAGAGAGGTCA[A/T]ACAACAAGGAAGTCA | 57097 |
rs543789236 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3871856 | GGAAGGCCTCAGAAG[C/G]AGCCTCGGAAGCAGT | 57097 |
rs543801888 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3854989 | CAACATATGCAAATC[A/C]ATAAACGTAATCCAT | 57097 |
rs543824829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3813590 | ATGGCCTTTTTAGTA[A/G]TTATTTTTTAAATTA | 57097 |
rs543950450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3865330 | AAACCCATGTATTCA[A/G]CTGTTGATGGGTGAA | 57097 |
rs543957717 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3858344 | ACCATGCAGAGAAAG[A/T]GGCTGTAGACAACAT | 57097 |
rs543997045 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3849596 | CATATGTAGGAGCTA[A/C]ATAAGTGGAACTCAT | 57097 |
rs543998814 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3841986 | CGAAGGCCGGACAGA[A/G]CAATCTTCCCAGACA | 57097 |
rs544000328 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3816715 | AATGACTAGAATCCA[A/C]TCTAAGGAAATTCTG | 57097 |
rs544001790 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3873460 | CTCCGCCCCACTCCT[A/G]CAAGCTCGCCCCGCC | 57097 |
rs544072293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3855818 | AGCCCACATTGCCAA[A/G]ACAATCCTAAGCAAA | 57097 |
rs544166280 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3844138 | GTTTTAATTACCTAA[C/T]GTCCGTGTAACTGCT | 57097 |
rs544208051 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3849327 | CTAAAAGAAAAAAAA[C/T]CAGTACACTGAAGGG | 57097 |
rs544210410 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810341 | ATGCCTGTAATCTCA[C/G]CACTTTGGAAGGCTG | 57097 |
rs544258080 | in-del | -/AGG | 0.0146672 | 0.084371 | intron-variant | PARP11 | GRCh38.p7 | 12:3822387 | GCGGATCACGAGGTC[-/AGG]AGATCGAGACCATCC | 57097 |
rs544270044 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3809812 | AAGCAGCCTAGTGAC[C/T]TTGTCTCCAATTATT | 57097 |
rs544363698 | snp | A/C | | | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3874089 | AAGGATCTACCCCAT[A/C]GGAAATGAAAATTAA | 57097 |
rs544364690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3872964 | GTGAAGGGATGAGGC[C/T]GAAACATCACGGGAA | 57097 |
rs544389619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3850570 | AATAAAATGGTATAT[A/G]TACAGGCTGGATACG | 57097 |
rs544505197 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | PARP11 | GRCh38.p7 | 12:3852096 | AGCATCAACACCAAC[A/G]AAAAGGATATTCACA | 57097 |
rs544508166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3838277 | TGACCACAATGAAAC[C/T]AGAAACCAAAGAAAG | 57097 |
rs544570348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3831843 | CCAGTAAACTATTCA[C/T]AATTCCTACTGCTTT | 57097 |
rs544670689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3851251 | GGTTCATGTCATTGG[A/G]ACTGGTTGGGCAGCG | 57097 |
rs544797169 | in-del | -/A | 0.0637235 | 0.166737 | intron-variant | PARP11 | GRCh38.p7 | 12:3849258 | TTATGGAGGTACCTC[-/A]AAAAAAAAATAGAAC | 57097 |
rs544861998 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3835765 | GAAACACTCTAGAAA[C/G]GCTCAGTGGTAGATT | 57097 |
rs545009392 | in-del | -/T | 0.00953873 | 0.0683987 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3875107 | TAGATGCATTAACAA[-/T]TTTTTTTCAGATCTG | 57097 |
rs545039201 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3874750 | TGGAATTAATTCCTG[G/T]AAATAAAATAGTTTA | 57097 |
rs545160063 | in-del | -/CT | | | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3869722 | TACACTGTCATAGTA[-/CT]CTTTTTCTTTCATAT | 57097 |
rs545179313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3812672 | CAGTCCTCACCACCA[A/G]CACCATCCCCTGCCC | 57097 |
rs545323866 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3855245 | GGATGCCCTCTCTCA[C/T]CACTCCTATTCAACA | 57097 |
rs545333893 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PARP11 | GRCh38.p7 | 12:3819982 | GAGATGCCCTTCTCC[C/T]ATCCAACTGGTGTCT | 57097 |
rs545380488 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PARP11 | GRCh38.p7 | 12:3867562 | TTCAGGGCCAAAATA[C/T]CCTGATTTTTAATGC | 57097 |
rs545388674 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3874295 | GCAGAACCTCGCTCT[C/G]TCGCCCAGGCTGGAG | 57097 |
rs545395821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3827221 | ACTGCAAAGAGTACA[C/T]GTGAAATGCTAATAT | 57097 |
rs545426522 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3865658 | CCTTAACAACAATAA[A/G]CCACTCACACTTTCT | 57097 |
rs545430178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3826767 | GAAAACCTGGCTAGA[C/T]CCAGTACAAACTTAC | 57097 |
rs545447994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3834357 | AAAACAGTGGGCCGG[A/G]TGTGGTGGTTCATGC | 57097 |
rs545476737 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3833645 | TGCTGAAAATTTTTT[A/T]AAAAAACAAACATTT | 57097 |
rs545526874 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3823069 | GTTGAGGGATTTAAT[A/T]GCAAAAGGCTGAACA | 57097 |
rs545540143 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3840031 | ACTAGCCTGCCTTTG[C/G]CTAGAAAGGTTCTTA | 57097 |
rs545556968 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3853763 | TATCCAGGACTTGCA[C/G]TCAGCTCTGCACCAA | 57097 |
rs545560877 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | PARP11 | GRCh38.p7 | 12:3857125 | CACACCAGGGCCTGT[A/C]GGGGGGTGGGGGGCT | 57097 |
rs545586573 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3809695 | TTTTGGTATGTAAAT[C/T]ACAAATAAATCGAAA | 57097 |
rs545590932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3861029 | AGGGTCACAGCTGGA[A/G]GAGAATTTGCCTCAG | 57097 |
rs545626302 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3820640 | AGGGCTGATGAAGAA[A/T]AATGAATTAAATTTT | 57097 |
rs545651307 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PARP11 | GRCh38.p7 | 12:3851266 | GACTGGTTGGGCAGC[A/G]GGTGCAGCCCACAGA | 57097 |
rs545678836 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | PARP11 | GRCh38.p7 | 12:3849568 | GGAAAGACAAATATC[-/A]CCTGTTCTCATTCAT | 57097 |
rs545751215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | PARP11, LOC105369609 | GRCh38.p7 | 12:3872413 | TACAATGGGTGGTGA[A/G]GAAAGGTACTAAAGT | 57097 |
rs545762242 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3855935 | AAAACAGAGATATAG[A/G]CCAATGGAACGGAAC | 57097 |
rs545803349 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PARP11 | GRCh38.p7 | 12:3852063 | TGTTAGAAGGAAAAC[C/T]AACAAACAGAAAGGA | 57097 |
rs545872707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3830850 | TGGCTTCAGGGTCTA[C/T]GCACTTAGCCGCCGT | 57097 |
rs545875085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3855167 | TATCACAAACCCACA[A/G]CCAATATCAAACTGA | 57097 |
rs545875344 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PARP11 | GRCh38.p7 | 12:3862569 | AGTTTATAAATTTTT[C/G]TATACTATATATTTT | 57097 |
rs545934276 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3828331 | AGGCGGGTGGATCAG[A/G]AGGTCAGGAGTTCAA | 57097 |
rs545940440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3861881 | TACAAAAAAATTAGC[C/T]AGGCGTGGTGGAGGG | 57097 |
rs545993074 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3858014 | GCAGTTGCCAACACT[C/T]GGAAAACAATGACTG | 57097 |
rs546045048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3816754 | AAAAGATACAAAAAT[C/T]AGCTGGGTGTGGTGG | 57097 |
rs546100382 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PARP11 | GRCh38.p7 | 12:3856447 | CAAACAACCCCATCC[A/G]AAAGTGGGCAAAGGA | 57097 |
rs546187264 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PARP11 | GRCh38.p7 | 12:3849674 | GGGAGAGACTGATTA[A/G]AAGAGGTTGATTAAT | 57097 |
rs546225225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3814600 | ATGCTTTTTATCCTC[A/G]GAAACTAGAAAATGT | 57097 |
rs546248492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3822336 | GGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 57097 |
rs546250363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3845890 | GTCTTAATGCTGGGA[A/G]GCAGCAACTTTGGGG | 57097 |
rs546267864 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3852141 | ATAGGTCACCGTCAT[A/C]AAAGACCAAAGGTAG | 57097 |
rs546286793 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3813700 | GACCAGAAAATTAAA[G/T]GTACATCCCATACCT | 57097 |
rs546324474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3871267 | AGTTATCTCAGCATA[A/G]GAGTAGTTTCTTATG | 57097 |
rs546371577 | in-del | -/T | 0.222035 | 0.248431 | intron-variant | PARP11 | GRCh38.p7 | 12:3825109 | AATTAACATGCTACC[-/T]TTTTTTTTTTTCCAG | 57097 |
rs546623436 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PARP11 | GRCh38.p7 | 12:3831917 | AGAGAGAAGGAAAGA[A/C]AGTGTGACCTAAATT | 57097 |
rs546653499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3845039 | TTGAGTTGGAAATTA[C/T]GAAACTTCACCATAT | 57097 |
rs546688723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3831304 | ACACATAAAAACATA[C/T]AGAGTTATTGATGAT | 57097 |
rs546698098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3872164 | CAGAGAGGCCAAGAA[A/G]AATCTGAACAAACAG | 57097 |
rs546745611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3858567 | CTACTTGGTCCCTCA[A/G]TCGCTTCTGATGTTT | 57097 |
rs546764857 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | PARP11 | GRCh38.p7 | 12:3866858 | CTACTGGATGTCATA[C/T]ATTATCATGCTATAT | 57097 |
rs546786020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3844207 | ATTTTAGAGAGCACT[C/T]TGAAAGATAACATTT | 57097 |
rs546795421 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3873847 | CCTTTACATACTATC[C/G]CTGCCCTCAAGATTT | 57097 |
rs546808804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3857606 | CTCACTGTATTCAAG[A/G]AGTAAATTTCTTACC | 57097 |
rs546852194 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3833882 | GGCTTCCAGTCTGTG[C/G]CTAGTTTTACCCCGG | 57097 |
rs546852423 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3826093 | ATTTCCAGTCTATTT[G/T]TTTTTCTGTCCAATA | 57097 |
rs546896069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3865403 | TGTTCAAGTTTGTTA[C/T]ACTGTTGCTCATTTT | 57097 |
rs546924998 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PARP11 | GRCh38.p7 | 12:3817364 | TACTAGATTAGATGG[C/T]GCATATATACCAGTT | 57097 |
rs546937135 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3825201 | AAAATAGGAGACATG[A/C]TTTAAGATTTTTTCC | 57097 |
rs547015272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3828319 | TTTGGGAGGTGGAGG[C/T]GGGTGGATCAGGAGG | 57097 |
rs547022953 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3873147 | AGCAGTTCCGGTGAC[A/C]CCCTCCCGCCCCTCT | 57097 |
rs547051507 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3809870 | AAGCGCTTTTTCTAA[A/C]TATTCTCAGCACTTC | 57097 |
rs547170875 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3861799 | GGAGGCCGAGGCGGG[C/T]GGATCACGAGGTCAG | 57097 |
rs547193705 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3809932 | GCCAGGAAATCTTTG[C/T]TGCCACTTTGTTTCA | 57097 |
rs547251302 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PARP11 | GRCh38.p7 | 12:3821758 | ACCAGGTCAAAATAC[C/G]GCAAGAGAAAAACAG | 57097 |
rs547291811 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3815454 | AAATTTGAACACCTA[C/T]CTAGGCTTTCTTTTC | 57097 |
rs547294405 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PARP11 | GRCh38.p7 | 12:3824128 | ATCTGTTTTCCCACA[A/T]CCACTCCAAAAAGGT | 57097 |
rs547301935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3864751 | AGAATATGTAGTGAT[A/G]TTACCTCTCTCATTC | 57097 |
rs547304057 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3836210 | TCTTAAAATCAGCAA[A/G]AGAAAAACAACTGAT | 57097 |
rs547336655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3813222 | GGAAACCGATGGCCT[A/G]CAGGGATTCTTTTAA | 57097 |
rs547349137 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PARP11 | GRCh38.p7 | 12:3829468 | ACTTTTGTGAGTTTC[A/G]CTTTCCTTGACTGTA | 57097 |
rs547357906 | snp | C/T | 0.000484994 | 0.0155648 | intron-variant | PARP11 | GRCh38.p7 | 12:3828884 | AATATACTAAAAACA[C/T]ACAACTATTAGGGAA | 57097 |
rs547388603 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3820987 | TAATTCTCAGGTATA[C/T]AGAAATGAAATGAGT | 57097 |
rs547401271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3861383 | TGCCAATCTGATAGA[C/T]GGGCAGTATTGTGGT | 57097 |
rs547434987 | in-del | -/AAGT | 0.00557542 | 0.0525036 | intron-variant | PARP11 | GRCh38.p7 | 12:3830221 | CTTAACAATTTAGGC[-/AAGT]AATAATAATCTTAGG | 57097 |
rs547458748 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3835254 | AGTACATAGTCTATG[A/C]CAATCCAGAAATGCC | 57097 |
rs547475639 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3875301 | CTATGAAAAAATGTC[G/T]TGTTAGTTCTAATAG | 57097 |
rs547582592 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3827166 | CCATTTTTATAGAGA[A/C]AACCTGAGTTGGCTA | 57097 |
rs547586347 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3861949 | AGAATGGCGTGAACC[C/T]AGGAGGCAGAGCTTG | 57097 |
rs547607516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3813841 | GCTCACTAATATTCT[C/T]ACCTATGATTTTCTT | 57097 |
rs547626378 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3854880 | TCAACGCAAAAATCC[C/T]CAATAAAATACTGGC | 57097 |
rs547638958 | in-del | -/A | 0.00557542 | 0.0525036 | intron-variant | PARP11 | GRCh38.p7 | 12:3838799 | CGTGGTGGGGAAACG[-/A]AAAGGCCGCGTCTTT | 57097 |
rs547769841 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3853159 | TGGAAAGGAACAACC[A/C/G]GTACCAGCCACTGCA | 57097 |
rs547827277 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3857362 | AGCAACAGAGAAATT[C/T]ATTGATGAGTTTGCC | 57097 |
rs547880057 | snp | A/G | | | intron-variant, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3815021 | GGAAAGAAGGAGAGT[A/G]GGACAGGGATGGAGT | 57097 |
rs547894686 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3818562 | ATTAAATTTTAAAAA[C/G/T]ATAACATAACAATAA | 57097 |
rs548004319 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3815172 | ATTTCATAAAAATCA[A/T]ATTTTAAAAATTAAA | 57097 |
rs548132434 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3874319 | GCTGGAGCGCAGTGG[C/T]GCCATTTTGGCTCAC | 57097 |
rs548149363 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3853812 | TACAGAACTCTCCAC[C/G]CTAAATCAACAGAAT | 57097 |
rs548159604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3850760 | AAGCATTTATATTTA[C/T]CTACAAAACAGAAAG | 57097 |
rs548359696 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3871986 | CTAGGATCCCTCTCC[G/T]ACAAAGCAAGCCATA | 57097 |
rs548374737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3871642 | AACTTGCTGAAATGT[A/G]ATTCTACCATTTTTC | 57097 |
rs548377042 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3823644 | AAGCTGGCTGGGCGC[A/G]GTGGCTCATGCCTAT | 57097 |
rs548437120 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3822837 | AAAAGGCTGAAACTC[A/G]TATTTATATTGTCTA | 57097 |
rs548542526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3851308 | AGAAGGGCAGGGCAT[C/T]GCCTCACCCAGGAAG | 57097 |
rs548546546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3843587 | TAGTTCTTTTCTAGA[A/G]GATGCTGCTAGAAAA | 57097 |
rs548670262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3840319 | AGCTGGAACACAGTG[C/T]CAGGGAAGAAGATGA | 57097 |
rs548719842 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3858092 | GTTGATGATGAACAA[C/T]TGGTGATTTCGAAGG | 57097 |
rs548728872 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3868757 | ACATAGTCCAAGTCA[C/T]CTTCGTCTCTACCCT | 57097 |
rs548825630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3831063 | TCCTGTCCTCATTCT[C/T]TGAGGGTTTTTAAAT | 57097 |
rs548827663 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3822524 | GAATGGCGTGAACCC[A/G]GGAGGCGGAGCTTGC | 57097 |
rs548863201 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3836634 | TACATGAACTGCCAG[G/T]TCCAAGATGGTGGCA | 57097 |
rs548890352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3830316 | CAGGTTTCAGCATAG[C/T]CCCAAGCATTTTCAA | 57097 |
rs548905191 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3874423 | GCCACCACGTCCCGC[A/G]AATTTTTGTATTTTT | 57097 |
rs549012741 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3833973 | TGGAGAGGTGACACA[C/G]AGGACCCGTCTCTCT | 57097 |
rs549041084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839840 | AGGTATTTAAAACTG[A/G]TGTTAGTAAAATTGT | 57097 |
rs549056771 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3824419 | AGCTATGACCAAAAA[A/T]TTTTTTTAGTTTTTA | 57097 |
rs549218007 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3818265 | CCTACACTTCATTCG[C/T]TGTAGGTGACCTCCC | 57097 |
rs549227976 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3819627 | TTTCTAAAATGCAGA[A/T]CAGATCCATCACTCT | 57097 |
rs549260902 | in-del | -/C | 0.0023933 | 0.0345097 | intron-variant | PARP11 | GRCh38.p7 | 12:3819558 | GCAGGTAAAATCACT[-/C]CCAGTTGAGAACCAC | 57097 |
rs549289311 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3827031 | CTTTCTGTGTTCTCC[C/T]AGACTCTACACATAC | 57097 |
rs549340869 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3817933 | GCTAGTAAATTCCAC[C/T]GGCGATTCTGACCTG | 57097 |
rs549346113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3865449 | ATCAATTATTTGGAG[A/G]AAACTACTGAAATCT | 57097 |
rs549395663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3821807 | AATTAATACAATTCA[A/G]TATTTATGTTTTAAC | 57097 |
rs549437090 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3866575 | ATATCCCATTATATT[A/C]ACTCTCTGTTGATAC | 57097 |
rs549462244 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3831988 | TGAGATTGGAGCTAA[A/T]AGTTAAGAAAAATAT | 57097 |
rs549537348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3872661 | AGAACTGATGGCTCC[C/T]CTTAGGCCCATTCAA | 57097 |
rs549572847 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PARP11 | GRCh38.p7 | 12:3826521 | CCCTTCTGTATCACA[C/G]TTAGGTTAAACAGAC | 57097 |
rs549613450 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3809990 | ACTACTTACCTCCCA[C/G]TGCACAATTACACAT | 57097 |
rs549614959 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3866101 | TTTCCTACCCATCAT[A/C]ACTTAAAAACAAACA | 57097 |
rs549616594 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3828375 | AACATGATGAAACGC[A/T]GTCTCTACTAAAAAT | 57097 |
rs549622592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3814933 | AAATAATACTGTGTA[C/T]TATGTAGGTATACAT | 57097 |
rs549741182 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PARP11 | GRCh38.p7 | 12:3844270 | GACTGGGATGGTTGT[A/G]TGGAAAACATTTTTT | 57097 |
rs549842363 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PARP11 | GRCh38.p7 | 12:3829152 | ACTTACTAATCACCT[G/T]TTCTAGTTCCCAACA | 57097 |
rs549850909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3836036 | ATATACACACACACA[C/T]ATATATATATACACA | 57097 |
rs549856627 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PARP11 | GRCh38.p7 | 12:3855557 | AAAATACCTAGGAAT[A/C]CAACTTACAAGGGAT | 57097 |
rs549948801 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3853599 | ACTATCCTAAATATA[C/T]ATGCACCCAATATAG | 57097 |
rs549969193 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3850635 | GCCAATATCTATGTG[C/T]ATTACTGTGTTTTTT | 57097 |
rs549993268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3853951 | TCTCAGACCACAGTG[C/T]AATCAAATTAGAACT | 57097 |
rs550101009 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PARP11 | GRCh38.p7 | 12:3854515 | ATGAACACCTCTACG[C/T]AAATAAACTAGAAAA | 57097 |
rs550148703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3862659 | CGTTCATTTTTCTGC[A/G]TATGGGTATCCAATT | 57097 |
rs550174023 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3809441 | TCTTACAATGGCTAC[G/T]GCAGTGCATTCTACA | 57097 |
rs550231269 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3812730 | GTTTTTAAAATAAAT[C/T]TTACAAAGAAAACAA | 57097 |
rs550259407 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3824105 | TTCTCACCAGAAATA[C/T]AGAAATCATCTGTTT | 57097 |
rs550281951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3851819 | TCCTCAAGTGGGTCC[C/T]TGACCCCCGTGTAGC | 57097 |
rs550313899 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3820192 | CAGTGCTTGTCATAA[A/T]GTAGGTACTAAGACA | 57097 |
rs550474288 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3841633 | TCTGAGACCCCTGGG[C/T]AGCTTCTGCATGCTG | 57097 |
rs550504745 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3841054 | ACCCCTGGACCTGAT[G/T]CTGCTGTATCCCAAA | 57097 |
rs550594008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3837443 | CCATAATGCAAAAAC[C/T]TATAATAGACCCACT | 57097 |
rs550654339 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | PARP11 | GRCh38.p7 | 12:3808744 | CATATGAGTTACAGG[C/G]AACAAACTCCTTGGG | 57097 |
rs550657228 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PARP11 | GRCh38.p7 | 12:3843312 | GAAATGTAGATGCTA[C/T]GCATTTTGAAAATAA | 57097 |
rs550657297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3836684 | CTCCCTGCCCCCACA[A/G]AAAACCAAAAACAAA | 57097 |
rs550669360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3842529 | TTGACGGTTGTTGCC[A/G]AAGTATTTTCTAACA | 57097 |
rs550698594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3857475 | GAAAGACACCAATTA[C/T]AGCTGCTGAGACAGC | 57097 |
rs550715153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3816918 | AAAAGAAGGCCAGGC[A/G]CAGAGGCTCACGCCT | 57097 |
rs550722367 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3864693 | CATACTGCTTGATAT[A/G]AAGTTGTTCATAACA | 57097 |
rs550765290 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3872576 | CACTTTGTCCACCGA[A/G]CGAAAACATCTAAGA | 57097 |
rs550783741 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, utr-variant-5-prime | PARP11 | GRCh38.p7 | 12:3863882 | AGGCAGGTCTTCACC[A/G]TAAACTGCATTGCTA | 57097 |
rs550852950 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3856941 | CACCACGGAATACTA[G/T]GCAGCCATAAAAAAG | 57097 |
rs550888674 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839178 | CCGCCTGCCGCCTGC[A/C]GCCGCTCGCGGAGCC | 57097 |
rs550902692 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3838696 | AGATAAACAAAAATG[C/G]ACAATTCTTAGTCTT | 57097 |
rs550905034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3844976 | GTTGACATATTTCTT[C/T]ATAAGAGAATAGAGG | 57097 |
rs550937420 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3828389 | CTGTCTCTACTAAAA[A/C]TACAAAAAAATTAGC | 57097 |
rs550971079 | snp | A/C | | | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3870826 | GGACTGATAACAAAA[A/C]GGGAATAATAGCTAC | 57097 |
rs550974994 | snp | A/G | | | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3869991 | ACAAAGGGATGATTC[A/G]TGGCCCCAGGCAGGA | 57097 |
rs550994385 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3834580 | CAAAGGTTTCAGTGA[A/G]CCAAGATCACACCAT | 57097 |
rs551055704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3840983 | GTGAACCTACAACTT[C/T]TGGACCAACAGGTGT | 57097 |
rs551073970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3840341 | AGAAGATGAAAAAAC[C/T]TTCCACTTCTGGACA | 57097 |
rs551117250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3861304 | TGAAAATGGGGCCTT[C/T]GGGAGGTGATTAGAT | 57097 |
rs551174954 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3855487 | ATTCCTACACACCAA[C/T]AACAGAGAGCCAAAT | 57097 |
rs551203792 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3818423 | TATGTTCTCAGAATT[G/T]CATCTCACCACACTT | 57097 |
rs551342241 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810573 | GCAGCCTGGGCAACA[A/G]AGCAAGACTCTGCCA | 57097 |
rs551389110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3827090 | AAGATCATCTCAGCA[C/T]GTGGAGCAAGACCTG | 57097 |
rs551405913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3818492 | TTCTCTAAGTCTTTT[A/G]AATTCTCCTTCTCCA | 57097 |
rs551406897 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3827628 | AAAAATGGCTTGTCA[A/C]GAGCAAGGATCTAAT | 57097 |
rs551513343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3854046 | GACTACTAGGTAAAT[A/G]ACTAAATGAAGGTAG | 57097 |
rs551541523 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | PARP11 | GRCh38.p7 | 12:3825983 | ATCAGGCCGCCTCGG[C/G]CTCCCAAAGTGCTGG | 57097 |
rs551550872 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3829681 | TCACATTCACCCTCT[A/C]TTGTTTCTTCTAAAT | 57097 |
rs551581069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3813073 | ACCTCCCAAACTGCT[A/G]GGATTACAGGCGTGA | 57097 |
rs551598372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3820912 | AAATGTACGCAGGCC[A/G]TATTAACTAGTCAGA | 57097 |
rs551626829 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3811413 | CCCTGATGGATGAAG[C/T]GTAGGCTAATGACAT | 57097 |
rs551769219 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3853019 | CAACCCAGAATTTCA[C/T]ATCCAGCCAAACTAA | 57097 |
rs551872531 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3825482 | CTACCTAATTCTTAC[A/C/G]GCCCCAGTAATTGTA | 57097 |
rs552032797 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3846066 | AAAAAGTATATATAC[C/G]TATCTTTTGAAGTGT | 57097 |
rs552034562 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3862813 | ATGCCAATACTACAC[C/T]GTTTTGATTATTGTT | 57097 |
rs552173156 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3842606 | AAAGTAAAAACCCCA[G/T]TTGGAACTCTTTCCT | 57097 |
rs552209262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3822513 | CTGAGGCAGGAGAAT[A/G]GCGTGAACCCGGGAG | 57097 |
rs552221809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3862826 | ACTGTTTTGATTATT[A/G]TTGCTTCACATTGAA | 57097 |
rs552234677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3849954 | GTATATCGATTATGT[A/G]TCAACTTTTTAAATA | 57097 |
rs552300268 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3854594 | AAACCAGGAAGAGGT[A/T]GAATCCCTGAATAGA | 57097 |
rs552322207 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PARP11 | GRCh38.p7 | 12:3859288 | TGGCAGATGTAGGCC[A/G]GTGCAGTGGCTCACG | 57097 |
rs552371791 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3848539 | CAACAAAGTCACCAC[G/T]AACATAGAATGGGAA | 57097 |
rs552505223 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3833146 | AATTTATTTTGTTAG[C/T]ATGAGTATAGTATCT | 57097 |
rs552514175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3849120 | AATGAGACATCATCT[C/T]ACCTCAGTTAAAATA | 57097 |
rs552550951 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3856789 | CTGGGTATATACCCA[A/T]AGGATTATAAATCAT | 57097 |
rs552770093 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3838769 | ACCCGCTCCCCGCCC[A/C]TCCGGCGCCCTCCAG | 57097 |
rs552835300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3844409 | GAGAAGATAGAGGGT[C/T]CTCCACTTTCAGCTT | 57097 |
rs552840302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3836560 | GCGCTGGTAAAAGGT[A/G]TAATTGCTGATTTCT | 57097 |
rs552845462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3842012 | AGACACGAAAGGCAG[A/G]TATGGCATTGGCTTC | 57097 |
rs552894717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3866169 | TTCACATTACTAAAT[C/T]CTATGCTCTTTTCAG | 57097 |
rs552941553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3856512 | GCAGCCAATAGACAC[A/G]TGAAAAAATGCTCAT | 57097 |
rs553081572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3831621 | CAATGAAGGGGGTTT[A/G]TTATTTTTTATATAT | 57097 |
rs553104777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3851512 | TTGCTCACTGCTAGC[A/G]CAGCAGTCCGAGATC | 57097 |
rs553128002 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PARP11 | GRCh38.p7 | 12:3823481 | TTATTCCTAGTGCTT[A/C]CGACAGAGCCTGGCA | 57097 |
rs553193728 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3858733 | ACTGCTTAGTTATCC[A/T]GAACACATTATTTTT | 57097 |
rs553206186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3858063 | ACACAACCTGGCCTA[A/G]GACTATGTTCAGTGT | 57097 |
rs553220812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3817134 | AGGCGGAACTTGCAG[C/T]GAGCTGAGATCGCGC | 57097 |
rs553280465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3857044 | CAGAAAACCAAACAC[C/T]GCACGTTCTCACTCA | 57097 |
rs553289853 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | PARP11 | GRCh38.p7 | 12:3862481 | GTATTTTTTTTTCTA[-/T]TTTTTTTCACCTGGA | 57097 |
rs553292083 | snp | C/G | 0 | 0 | intron-variant | PARP11 | GRCh38.p7 | 12:3825588 | ACCATAAGGCATTTT[C/G]TAACTGCAAACTGTT | 57097 |
rs553342023 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PARP11 | GRCh38.p7 | 12:3853602 | ATCCTAAATATATAT[C/G]CACCCAATATAGGAG | 57097 |
rs553386029 | snp | C/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3833907 | CCCCGGGAAGGGCAG[C/G]CTGCTGGTGTTTCTC | 57097 |
rs553390708 | in-del | -/TT | 0.00199481 | 0.0315187 | intron-variant | PARP11 | GRCh38.p7 | 12:3835292 | AGTCAGGTTAAGAGG[-/TT]GGAAAAGTCTGAGCT | 57097 |
rs553404206 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3816125 | AGAACTTCCTTTTTC[A/C]GAACTTTATGTTCTC | 57097 |
rs553420794 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3850526 | CTCACATGTCCAGAT[A/T]CCCCCACGCAAGCAT | 57097 |
rs553426222 | in-del | -/CT | | | intron-variant | PARP11 | GRCh38.p7 | 12:3836792 | AGAGGAATGAAAAAA[-/CT]CTGAGCAGACAGTAA | 57097 |
rs553431563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3822828 | GATGAAAACAAAAGG[C/T]TGAAACTCGTATTTA | 57097 |
rs553454099 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3827110 | AGCAAGACCTGTGAT[C/G]CCATCTTCTTGGACC | 57097 |
rs553478324 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810337 | GCTCATGCCTGTAAT[C/T]TCAGCACTTTGGAAG | 57097 |
rs553482619 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PARP11 | GRCh38.p7 | 12:3843931 | ATGTGTAATACACCT[A/G]GCCAAAACCAGATGC | 57097 |
rs553564695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3847594 | ATCATTTTAATAGAT[A/G]CTTTAAAAGCATTTG | 57097 |
rs553575912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3819792 | TAAGGCTACTAAAGA[C/T]GATCACACAACCACC | 57097 |
rs553640605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3841310 | AGGCATACAGTTGTC[C/T]TGTGTGGGCCCCACA | 57097 |
rs553755884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3820308 | CTATATGGTGAGTCA[C/T]AGGTTATGTGACAGT | 57097 |
rs553836595 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | PARP11 | GRCh38.p7 | 12:3846274 | CTGTGTGCATATATT[A/T]AAAAAAAAAAAGAAA | 57097 |
rs553912229 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3826449 | CTTCATTGCTTGACG[A/T]AAGCTCACACATAAA | 57097 |
rs553999018 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810225 | AGAGAGAAAATTCAG[A/C]ATTAGAAGGAGTTAA | 57097 |
rs554149784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3845509 | GAAAACATTCAGCCA[C/T]CCTAGAAACTAGCAA | 57097 |
rs554285522 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3842300 | GATCCAAGCAGTTCT[A/G]TAATCAAACTTATGG | 57097 |
rs554308810 | snp | C/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3864123 | CCTTTCTATTCCTAG[C/G]CTGCTGAGAATTTTA | 57097 |
rs554334040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3851970 | CTGTTCTGCAGCCTC[C/T]GCTGGGATACCCAGG | 57097 |
rs554442873 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3874109 | ATGAAAATTAAACAG[A/C]TCATTATAGATCCTT | 57097 |
rs554549213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3837565 | ACAACCAGAAAATAA[A/G]CAACAAAATGAACTA | 57097 |
rs554620277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3850135 | CCACAAGAAGAATCA[C/T]AGTAAATAAGATGGT | 57097 |
rs554625374 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PARP11 | GRCh38.p7 | 12:3836931 | ATTAAGGTGGCCAAC[C/T]AGCTTTCCCACCATC | 57097 |
rs554665540 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3870214 | CACGTAGAATGTTGA[C/T]TTTTAAAACCAAATT | 57097 |
rs554686667 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3871795 | GAAAATACTACCCCG[A/C]AGTATGACACTTTGG | 57097 |
rs554815154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3871812 | GTATGACACTTTGGC[A/G]TGCTGAATACTTTGA | 57097 |
rs554919891 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3873877 | TTATAATCTAGAAAA[C/G]AAAGCAAAAAGTAGT | 57097 |
rs554928860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3861762 | AGGCGTGGTGGCTCA[C/T]GCCTGTAATCCCAGT | 57097 |
rs554940561 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3866219 | ACGGTAACATTTCAC[A/C]GTTTATCCTCTGTCC | 57097 |
rs554969547 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PARP11 | GRCh38.p7 | 12:3828504 | AGTGAGCCGAGATCA[C/T]GCCACTGCACACCAG | 57097 |
rs555089113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3841732 | GGCCCAGTTCCTATT[A/G]CACCTCCTTTCTTTC | 57097 |
rs555149593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3832686 | TAACTTTAAAATATC[A/G]CAACCATAGTAAGAA | 57097 |
rs555191628 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3855740 | CATCCCCATCAAGCT[A/C]CCAATGACATTCTTC | 57097 |
rs555207549 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3870950 | TTTGCTAAAATCAAA[C/T]ACAAGTAATTACTTT | 57097 |
rs555211372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839357 | GCGGCGCGGGGCCCC[A/G]CGAGGACGCGACGCC | 57097 |
rs555231548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3852487 | CAAGAACTATGTGAC[A/G]CATGCACAAGCTTCA | 57097 |
rs555303141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3851185 | GTCCACAGCTCCCAG[C/T]GTGACTGACACAGAA | 57097 |
rs555303948 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3873334 | CGGGAGCGAAGGGAC[A/G]GAGATGCAACCTTTA | 57097 |
rs555365238 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3836513 | TGATACTAGGCATTC[A/G]TAATAATCCATGGGG | 57097 |
rs555376520 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PARP11 | GRCh38.p7 | 12:3817060 | GCCAGGCGTGGTGGC[A/G]GGCGCCTGTAGTCCC | 57097 |
rs555437341 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3857736 | TCATGCTTACTGCAG[A/C/T]GAAGCTAGACTGTAA | 57097 |
rs555480937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3832189 | CTTTCTGTTATAAAT[C/T]GCTTTGGGTGGGACA | 57097 |
rs555630252 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810316 | AAAATCAGGCCGGGT[A/G]CAGCGGCTCATGCCT | 57097 |
rs555658176 | in-del | -/CCTGAGG | 0.00478085 | 0.0486577 | intron-variant | PARP11 | GRCh38.p7 | 12:3834413 | AAGATGGGCAGATCA[-/CCTGAGG]CCTGAGGCCAGGAGT | 57097 |
rs555691744 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3818638 | AAGCTTCTTGAAAAA[G/T]TTGTCAACATTTGCT | 57097 |
rs555755617 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3857126 | ACACCAGGGCCTGTC[A/G]GGGGGTGGGGGGCTG | 57097 |
rs555772530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3813270 | TTCTATGATATGGGA[C/T]AACAATTCAGTAATA | 57097 |
rs555834267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3812622 | TGGACAGCTGTAGTA[C/T]AGACTGCCATAGGAA | 57097 |
rs555846341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3820383 | GACACGCTGCCCTTA[C/T]AATGAGACTCAGTAT | 57097 |
rs555884803 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3836499 | TTATCAGGCTGAAAT[G/T]ATACTAGGCATTCGT | 57097 |
rs555889931 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3861981 | AGTAGGATGAGATAG[C/T]ACCACTGCACTCCAA | 57097 |
rs555895170 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3816864 | CTGAGATTGTGCCAC[C/T]GCACTGCAGCCTGGG | 57097 |
rs556021018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3860855 | CCAATTAATTTTTCA[A/G]TTTTTTCAGAGACAG | 57097 |
rs556039516 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3848091 | AATATAAAATACATA[C/T]GAGTCAATTTAACTA | 57097 |
rs556087088 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3848871 | TGAAGAAACAAGTCA[C/G/T]AGAATGGGAGAAAAT | 57097 |
rs556146932 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3861521 | ACTTTAAAAAATTGA[C/G]TTCCTTCTCTTGAGA | 57097 |
rs556285976 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3875125 | TTTTTCAGATCTGCA[G/T]CAGCATCTGTAAAAA | 57097 |
rs556406998 | snp | G/T | | | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3875053 | AAATTTTCAATATCA[G/T]GGGTCTTTCCATTCA | 57097 |
rs556409676 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3859808 | GAGTGGCTATACTAA[C/T]GCCAGGCAAAATAGA | 57097 |
rs556563291 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3819932 | CTGCGCTCCCTCTTA[C/T]ATCCAGACTTTGGTT | 57097 |
rs556588153 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PARP11 | GRCh38.p7 | 12:3834334 | CCCCATGCCTAAGGG[C/G]ATTATCAAAAACAGT | 57097 |
rs556664676 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3853207 | AAAGACCATCGATGC[C/T]AGGAAGAAACTGCAT | 57097 |
rs556679083 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839995 | TCAGGCAACGAGCAG[C/G]TGAAGAACAATGGGA | 57097 |
rs556722420 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3816395 | CAAGAAGAGAGCATG[A/C]ATGCCTTTCGAGTTA | 57097 |
rs556746339 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3851537 | GAGATCAAACTGCAA[A/G]GCAGCAGCCTGGCTT | 57097 |
rs556793507 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3869208 | AGGTCAGCTGATTAG[C/G]TAATTACCTCCCTTT | 57097 |
rs556810327 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3875358 | TACACAGACAATCAT[C/T]ATCACCTGCAAATAA | 57097 |
rs556811717 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3834831 | ACACTAGGCTGTGTA[C/T]ACCCAGGAATGATCA | 57097 |
rs556828773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3850886 | AAAGAGAAGGACCAA[C/T]TATGAAAGTTCTATG | 57097 |
rs556849014 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3874608 | CTTATGCGTATACTA[C/T]GTACACACAAATAGA | 57097 |
rs556894606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3872763 | TACAGGTTCCAAGGC[C/T]AGTTACTCCAATTAG | 57097 |
rs556970064 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PARP11 | GRCh38.p7 | 12:3832052 | AAAGAGAATAGAAAA[C/T]AGGAAAGTTCCCTTT | 57097 |
rs557033562 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3834941 | CACAAGGGTCTGAAT[C/T]ACCACCTCTGGCCAA | 57097 |
rs557098145 | in-del | -/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3841798 | TAGAAAATCCAGTAA[-/T]TGAGGCAGAATATTG | 57097 |
rs557183956 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3828653 | TGTGTTCCTTAGAAG[A/C]CAAGTATTAAATGCA | 57097 |
rs557187838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3865036 | AATTTCCCTCTAAGT[A/G]CTGCTTTGGCACCAT | 57097 |
rs557199041 | in-del | -/TT | 0.00438332 | 0.0466095 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3875301 | CTATGAAAAAATGTC[-/TT]GTTAGTTCTAATAGC | 57097 |
rs557199931 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3864258 | GCTGTTCAAATATTA[A/G]ACCTTGCATTCTTGG | 57097 |
rs557282573 | in-del | -/CT | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839722 | CCTGAAAAGGTGTTA[-/CT]GTGTTTTTCAAATGG | 57097 |
rs557323949 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3859373 | ATCGAGACCAACTTG[A/C]CCAACACGGTGAAAC | 57097 |
rs557325970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3868099 | ATTAGATATAAGTAC[C/T]TTGTAAGAAGCTGCA | 57097 |
rs557338206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3867303 | CTATTCAGAGTATGC[A/G]CTCTCAGATGTTGCA | 57097 |
rs557402863 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3830860 | GTCTACGCACTTAGC[C/T]GCCGTCATATACTGT | 57097 |
rs557421769 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3829585 | CAGAAGTGTTTAATA[C/T]GGATTTGTTCTTCCC | 57097 |
rs557424118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3822284 | CAATTAAATACAGCC[C/T]TCCGTTTCTTCATTT | 57097 |
rs557427208 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3851290 | CCACAGAGGGCAAGC[C/T]GAAGAAGGGCAGGGC | 57097 |
rs557443140 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PARP11 | GRCh38.p7 | 12:3833376 | GAGGCTGAGAAGGGA[A/G]GTTTGCATGAGGCCA | 57097 |
rs557475615 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3813746 | CTCCTTAATTTGCCT[A/G]AGTACCAGACATAAA | 57097 |
rs557503080 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3818667 | CTGTATACACAATAT[C/G]ATGTCTACCAACCTT | 57097 |
rs557565893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3826345 | TCATGGAGCTTCGGG[A/G]GTAGCTGGCAAGCAT | 57097 |
rs557592182 | in-del | -/A | | | intron-variant | PARP11 | GRCh38.p7 | 12:3834184 | AGTGTTACTCTGGGG[-/A]AAAAAAGACTCTCAC | 57097 |
rs557596707 | in-del | -/ACA | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839891 | AAGTAGCTGATGAAG[-/ACA]ACAGTGAAATATCAG | 57097 |
rs557627035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3846873 | GAGGATCATTTATGG[C/T]CAGGAGTTCAAGACC | 57097 |
rs557663354 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3859986 | ATTTGCTGAAGGAGT[A/G]GCCTGGGTCCTCCTG | 57097 |
rs557758226 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3853225 | GAAGAAACTGCATCA[A/G]CTAATGGGCAAAATA | 57097 |
rs557773623 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810037 | GAAATCTGGGATAGA[C/T]GGCACTTTAAGAATT | 57097 |
rs557806065 | in-del | -/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3824030 | GAGTCAAAGAATATA[-/T]TTTTTTCATGATTTT | 57097 |
rs557823804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3846866 | GAGGTAGGAGGATCA[C/T]TTATGGCCAGGAGTT | 57097 |
rs557823895 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3851905 | CCCCTCTGAGACGAA[A/G]CTTCCTGAGGAAGGA | 57097 |
rs557843945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3825849 | CTCCTGACTCAGCCT[C/T]CCGAGTAGCTGGGAC | 57097 |
rs557847243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3817116 | GAATGGCATGAACCC[C/T]GGAGGCGGAACTTGC | 57097 |
rs557906436 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3832948 | TGTCCGTAATGTTAT[A/C]TGTTACAAAGAGAAT | 57097 |
rs558015639 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839373 | CGAGGACGCGACGCC[A/C]ATGGACGCCTATCTG | 57097 |
rs558037652 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PARP11 | GRCh38.p7 | 12:3811687 | TGGATGATACTACTA[C/T]CTGAATTCAATTTAC | 57097 |
rs558153627 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3851599 | AGTAGGTAAACAAAG[C/T]GGCCAGGAAGCTTGA | 57097 |
rs558244683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3813325 | ATCCATGAAAAGATT[C/T]CTGAGAGAGTATAAT | 57097 |
rs558285684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3848966 | AACAGCAAAAGAAAA[A/G]AAAAAACACAAATAA | 57097 |
rs558288238 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3859330 | AGCACTTTGCGAGGC[C/T]GAGGCGAGTGGATCA | 57097 |
rs558293680 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3872542 | AAGAAGGCAGACTTG[C/G]AGTTGAAATGCTCCA | 57097 |
rs558295371 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3829673 | ACTCTCAGTCACATT[A/C]ACCCTCTATTGTTTC | 57097 |
rs558315479 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3857837 | AACATGTACTTTCCC[C/T]GAAATGTGACTTCAT | 57097 |
rs558408401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3836358 | AAAGCGCCTATCAAC[C/T]AAGAATCTTATACTA | 57097 |
rs558428244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3871914 | TCTCCTGCCCATCTT[C/T]CGTCCCAGAAGTGAG | 57097 |
rs558482477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3849525 | ATGAAATGAGAATTC[A/G]TTATGTCAAGTAAAA | 57097 |
rs558572353 | in-del | -/TC | 0.00199481 | 0.0315187 | intron-variant | PARP11 | GRCh38.p7 | 12:3869511 | CCAGCCACATAGGCT[-/TC]TCTCTTTTTCTCAAG | 57097 |
rs558603489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3855705 | GCCATACTGCCCAAG[A/G]TAATTTATAGATTCA | 57097 |
rs558620478 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3862020 | ATGGAGCGAGACTCC[A/G]TACCTAACCAATGCT | 57097 |
rs558752386 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3812766 | AAAACAGATAAAACT[C/G]GTTTAATGATTAAAA | 57097 |
rs558813739 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PARP11 | GRCh38.p7 | 12:3850310 | TAATTATATCAGTTC[A/G]AACACCCCTAATCCA | 57097 |
rs558821374 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3826311 | AAGATTAATAGCCAC[A/G]CTACGCGATGATCAG | 57097 |
rs558853390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3842216 | CAACTCTGTGGATAG[C/T]AGAGTGCAAAGACCA | 57097 |
rs558953140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3869293 | GGAGGCCATTATTAC[A/G]TCTACCATATTTTCT | 57097 |
rs559049028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3823703 | GATGGATTGCCTGAG[C/T]TTAGGAGTTCGAGAC | 57097 |
rs559053523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3847572 | AACCAAGAAGAAAAA[C/T]CATATAATCATTTTA | 57097 |
rs559056899 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | PARP11 | GRCh38.p7 | 12:3845100 | ACCAAAGCTCACCTG[-/T]TTTTTTGTGTTAGGT | 57097 |
rs559062794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3864414 | GGTTTTGAAATAAGG[A/G]TCTGACAGCCTTATG | 57097 |
rs559140727 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3840749 | GGACATAGTTGGATA[A/C]AAGACCCGAACCAAG | 57097 |
rs559198693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3861054 | CCTCAGGATGAATCA[C/T]ACCTTGGGCTCAACT | 57097 |
rs559274658 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PARP11 | GRCh38.p7 | 12:3815892 | AAATGATAGGCAGCT[C/T]GTTGAATATGTTTGG | 57097 |
rs559326423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3855940 | AGAGATATAGACCAA[C/T]GGAACGGAACAGAAC | 57097 |
rs559337610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3863683 | CCAAGCGTCCCTTCC[C/T]GGTGCAGTCACATGG | 57097 |
rs559351687 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3871942 | GAGTCACAGAAACCA[C/G]AATTCTTCCCCAAGG | 57097 |
rs559386438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3862570 | GTTTATAAATTTTTC[C/T]ATACTATATATTTTA | 57097 |
rs559389508 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3823567 | GACGCACAGAACTCC[A/G]CCATGTGGATACACC | 57097 |
rs559398842 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3816811 | GGAGGCTGAGGCAGG[A/C]GAATTACTTGAATCC | 57097 |
rs559487857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3844241 | TATGATGGTGCTAGG[C/T]AAAAAATTGTAAAGA | 57097 |
rs559560036 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3855106 | GCTAAAAACTCTCAA[C/T]AAACTAGGTATTGAT | 57097 |
rs559576988 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3851674 | GTAGACTCCACCTCT[A/G]GGGGCAGGGCATAGC | 57097 |
rs559623611 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3857116 | GGAACATCACACACC[A/G]GGGCCTGTCGGGGGG | 57097 |
rs559691759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3849697 | TGATTAATGGGTATA[A/G]ATATACAGTTAGATA | 57097 |
rs559720344 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3852761 | GGCAGGCCAACATTC[A/C]AATTCAGGAAATACA | 57097 |
rs559936520 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3837280 | TAGAGCTGAGAAAAA[A/C]CTGAGCGTAAGGCAC | 57097 |
rs559941711 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3874351 | GCAACCTCCGCCTCC[C/T]GAGTTCAAGCGATTC | 57097 |
rs560000835 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810418 | AACATGACAAAACCC[C/T]GCCTCTACTAAAAAT | 57097 |
rs560019300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3842429 | GGGATGAAGGTTATC[A/G]GTACCATCGAAATGT | 57097 |
rs560095938 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3845937 | GGATTAAAAATTGCA[C/T]TGTGTTACAGAGCTG | 57097 |
rs560155411 | snp | C/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3846406 | AAATTGGAAAACTTA[C/G]AAGAAATGGATAAAT | 57097 |
rs560156159 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3859383 | ACTTGACCAACACGG[A/T]GAAACCCTGTCTCTA | 57097 |
rs560196312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3818811 | GTAAACCACATTCTC[C/T]CTCCAGCTTCTGTGA | 57097 |
rs560250946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3834498 | CATTAGCCAGGTGTG[A/G]TGGCGTGCACCTGTA | 57097 |
rs560280095 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3860574 | TCATGGAACTTGCTC[A/G]GGACCTGTCACCCCT | 57097 |
rs560312651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3840780 | CATATTGGAGAATAT[C/T]ACTGATGATAAATAT | 57097 |
rs560336971 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3828140 | GCAATGTCCATTAAA[G/T]AAATTGTTTTCTGAC | 57097 |
rs560405059 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PARP11 | GRCh38.p7 | 12:3833895 | TGGCTAGTTTTACCC[C/T]GGGAAGGGCAGGCTG | 57097 |
rs560407606 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | PARP11 | GRCh38.p7 | 12:3844841 | GTTGGTTTCGCTTTT[A/T]TCCTTTAAGTTTGTT | 57097 |
rs560498380 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3857907 | AGGGTAAATATAAAA[A/C]TATATTCTTGAATAG | 57097 |
rs560526264 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, missense, nc-transcript-variant, upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3873228 | GGATTCGCTTCCCAC[A/G]TAACGGTGACAAAAT | 57097 |
rs560560789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3866510 | GAAATGTAAGATTAA[C/T]AATTTGTACGAAAAT | 57097 |
rs560625538 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3843716 | TTGCATGTTGTACTC[C/T]GTCCTCATTTGGAGA | 57097 |
rs560652679 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3862633 | TTATAGTATAGCAAA[A/G]TATGGAGTGACGTTC | 57097 |
rs560665620 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3838437 | TACCAAAATCTATGG[G/T]ATACAACAAAAGCAG | 57097 |
rs560674926 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3836487 | AATAAAGGAAGTTTA[C/T]CAGGCTGAAATGATA | 57097 |
rs560715948 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810419 | ACATGACAAAACCCC[A/G]CCTCTACTAAAAATA | 57097 |
rs560741846 | snp | A/C | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3873504 | CCATACGCGCGCGGG[A/C]GGTCGTCCTGGGCGG | 57097 |
rs560852578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3870399 | TGCTCTGCTGAAATT[A/G]GCAAAATCACACAGG | 57097 |
rs560892450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3821763 | GTCAAAATACGGCAA[A/G]AGAAAAACAGCATGT | 57097 |
rs560925091 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3863542 | TTGATGATTTCCTAG[G/T]ACTCACAAGACTCAA | 57097 |
rs561017256 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3811159 | GTCTCAAGCATCCCA[G/T]GCTTTCTATAATGTT | 57097 |
rs561096087 | snp | C/T | 5.3736e-05 | 0.00518316 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812077 | GAGCAAACCTTCCTG[C/T]AAAAAAGAATAAAGC | 57097 |
rs561140190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3871365 | CAAAGATTGTTAACA[C/T]TTTATTTTACTGTAT | 57097 |
rs561232401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3820833 | TGGCCAATAGACCCA[A/G]GACTATAAAGAACAC | 57097 |
rs561264867 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PARP11 | GRCh38.p7 | 12:3853876 | CCAAAATTGACCACA[C/T]AGTTGGAAATAAAGC | 57097 |
rs561284037 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3841560 | TTCACCTCTGGTTAT[C/G]CCTCCATCTCAGGTG | 57097 |
rs561348174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3820174 | TATCCCAAGTGCCCA[A/G]AACAGTGCTTGTCAT | 57097 |
rs561398540 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3872934 | CCGTCTCAAAAACAA[C/G]AACAACAACAAATGG | 57097 |
rs561457555 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3848996 | ATCCAATTTAAAAAT[G/T]GGCAAAAGACCTGAA | 57097 |
rs561469132 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PARP11 | GRCh38.p7 | 12:3854870 | CTGATGAACATCAAC[A/G]CAAAAATCCTCAATA | 57097 |
rs561501678 | snp | G/T | | | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3869810 | CTGCCTGCACCAGAC[G/T]GCAAACCCATAAAGG | 57097 |
rs561525191 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3858179 | AAAAAATGTACCTCC[A/G]GAGTCTATCAGTAAG | 57097 |
rs561566728 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3843483 | TTTCCCCTTGCACCA[C/T]TGGTTATGTATCACT | 57097 |
rs561635543 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3812898 | ACCTCCGCCTCCCAG[C/G]TTCAAGCGATTCTCC | 57097 |
rs561732471 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3857422 | AGAACAAGTCTATAA[C/T]GCCAATGAAACATCA | 57097 |
rs561760158 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3816848 | CGGAGGTTGTAATGA[G/T]CTGAGATTGTGCCAC | 57097 |
rs561769848 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3850533 | GTCCAGATTCCCCCA[C/T]GCAAGCATGTCCACA | 57097 |
rs561772613 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PARP11 | GRCh38.p7 | 12:3823809 | TAATCTCAGCTACTC[A/G]GGAGGCTGAGACAGG | 57097 |
rs561793838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3864680 | TGATCTAAGTTGTCA[C/T]ACTGCTTGATATAAA | 57097 |
rs561819121 | snp | C/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3828119 | TCAATCAGAAAATGA[C/G]AGAAGGCAATGTCCA | 57097 |
rs561827063 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3845646 | GAATACGTATTTGGC[C/T]ACACTATTTCTGTGT | 57097 |
rs561842246 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3809756 | TCTCTAACATTGTTT[A/T]TTGTGAACGGGTTTA | 57097 |
rs561850874 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | PARP11 | GRCh38.p7 | 12:3828628 | AATAAAACAACTGAT[-/A]ACGGTGTTTTGTGTT | 57097 |
rs561869002 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3835794 | TTTGTGAACAAGAAA[A/G]TATCAGCAAACTTGA | 57097 |
rs561878535 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839132 | CCCTACGCGCCCGGA[G/T]AGCGCGGACCGCTGC | 57097 |
rs561883259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3849761 | TGTTCAATAGATCAG[C/T]AGGGTGACTGTAGTT | 57097 |
rs561888143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3844952 | TTAACTGTTTATGTC[A/G]TACTGTATGTTGACA | 57097 |
rs561998867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3851692 | GGCAGGGCATAGCTG[A/G]ACAAAAGGCAGCAGA | 57097 |
rs562049744 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3815537 | AGGTCTTTCTTTATC[A/C]CAACAGTCTTTAGTT | 57097 |
rs562106510 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3840883 | CATGTGTCTTTGTCA[A/C]ATCCAGCTCCCCTTC | 57097 |
rs562164140 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PARP11 | GRCh38.p7 | 12:3847041 | ATGACTGCACCACTG[A/C]ACTCCAGCCTGGTCA | 57097 |
rs562228527 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3838154 | ATTGCTGGAGAATAC[A/T]CATTCTTTTCATCAA | 57097 |
rs562314582 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PARP11 | GRCh38.p7 | 12:3849989 | TTTAATTTTAAATAT[A/G]TATTTAATTAAATAC | 57097 |
rs562375154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3843088 | TCTGTCAAACTTGAA[C/T]AATGTCTTCTCTTTA | 57097 |
rs562387390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3831129 | CTTCTTGCAAAAAAT[C/T]AGAACTTTCAAAATA | 57097 |
rs562471187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3841038 | AGTGACACAGACTTT[A/G]ACCCCTGGACCTGAT | 57097 |
rs562486702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3841376 | CAGCCTGCAGGATGT[A/G]CCCAAAGGTCCCTGT | 57097 |
rs562514113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3825975 | GACTCGTGATCAGGC[C/T]GCCTCGGCCTCCCAA | 57097 |
rs562609546 | snp | C/T | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3875100 | GTATCTTTAGATGCA[C/T]TAACAATTTTTTTTC | 57097 |
rs562610361 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3824665 | CTGTCTTTGTTCTAT[A/G]GTTTGTACAGTCTGT | 57097 |
rs562625912 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3827478 | CTGTGCATATCATTC[A/C/G]GTTTCAGTTCTTCCT | 57097 |
rs562673893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3828164 | TTCTGACAAAGACAT[C/T]GAGAGAAAGATCACT | 57097 |
rs562785024 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3835143 | AAAAAATGTAAACTC[C/T]CTGAACTATAATAGC | 57097 |
rs562822693 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3833055 | AAAATCCTGGTCTAT[A/C]TAAGGAAAATAAGGC | 57097 |
rs562837257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3819060 | TCAACTCCTGACCCA[C/T]ATGTCAACTGCTGTA | 57097 |
rs562850184 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3818271 | CTTCATTCGCTGTAG[C/G]TGACCTCCCTTCTTC | 57097 |
rs562853469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3866637 | AATATAGTACTATAA[A/G]ACTCAAGTAAACTTT | 57097 |
rs562872569 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3833560 | AGTGAGCTAACATCA[C/G]GCCACTGCACTCCAG | 57097 |
rs562885505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839435 | CCAAGGACGGGTCGT[A/G]CCTGTTCCGGGCCGT | 57097 |
rs562970612 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3811364 | GATGCAATAAACACC[G/T]TGCACAGCAAGTCGT | 57097 |
rs562970837 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3822578 | CACTCCAGCCTGGGC[A/G]ACAGGGCGAGACTCC | 57097 |
rs563063167 | snp | A/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3818636 | CCAAGCTTCTTGAAA[A/T]AGTTGTCAACATTTG | 57097 |
rs563093720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3860229 | ATTTGAAATGAAAAA[A/G]TAGTAGATGGGAAGA | 57097 |
rs563110797 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3830805 | AGAGAGGTCATACAA[C/T]AAGGAAGTCAAGATT | 57097 |
rs563233244 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3815810 | AGTTAAGCTTTACTT[C/G]ATATAGTAATTTAAA | 57097 |
rs563254828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3871892 | CCTCTGATCTCCTGC[C/T]CTTCTGTCTCCTGCC | 57097 |
rs563267737 | snp | G/T | 0.0475351 | 0.146656 | intron-variant | PARP11 | GRCh38.p7 | 12:3822462 | AAATTAGCCAGGCGT[G/T]GGGGCGGGCGCCTGT | 57097 |
rs563315250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3871474 | CAGATTTCTAGGTTA[A/G]GAGCAATAGGCTATT | 57097 |
rs563332690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3857151 | GGGCTGGGGGAAGGA[C/T]AGCATTAGGAGAAAT | 57097 |
rs563348531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3861841 | CATCCTGGCTAACAC[A/G]GTGAAACCCCGTCTC | 57097 |
rs563381956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3830162 | AGCTTTCTATCTTTC[A/G]TATTGGCTCTGAAGA | 57097 |
rs563411649 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3870264 | ATATGCTTATAGGAA[C/G]AAAAACTATTAGTAG | 57097 |
rs563422665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3836546 | TAAAAAAGAAAAGAG[C/T]GCTGGTAAAAGGTAT | 57097 |
rs563427393 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3837108 | TCAATCAAAGGAGAC[A/G]ACACCAAATCAGAGT | 57097 |
rs563445810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3822996 | CAGTCAGTCAGTAAA[C/T]CTTAAAAACTATCAG | 57097 |
rs563490193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3850584 | TGTACAGGCTGGATA[C/T]GCCAATGGCAGGTTC | 57097 |
rs563541374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3854543 | AAATCTAGAAGAAAT[A/G]GATAAATTCCTGGAC | 57097 |
rs563697829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3854995 | ATGCAAATCAATAAA[C/T]GTAATCCATCACATA | 57097 |
rs563702940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3813639 | CAGCATATCCTGATC[C/T]TAAACAGTAGTCAGT | 57097 |
rs563762477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3813056 | GTGATCCACCTGCCT[C/T]GACCTCCCAAACTGC | 57097 |
rs563768313 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3821639 | TTTCAGCCAAGATGC[A/C]TAGCTCTAAACCTTG | 57097 |
rs563781226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3820900 | GAATAAAACCTGAAA[C/T]GTACGCAGGCCATAT | 57097 |
rs563834566 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3842377 | TATCAACATGTGAGA[A/C]GTGAGGAGTCCTGGA | 57097 |
rs563894813 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3842001 | GCAATCTTCCCAGAC[A/G]CGAAAGGCAGATATG | 57097 |
rs563917435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3852114 | AAGGATATTCACACC[A/G]AAACCCCATCTATAG | 57097 |
rs564014238 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3865916 | TGGTCCCACCTGTTC[G/T]TTGTTCTCTTTTTTT | 57097 |
rs564042793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3849104 | TGCAAACCAAAACCA[C/T]AATGAGACATCATCT | 57097 |
rs564097052 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810394 | CAGGAGTTTGAGATC[A/G]GCCTGGCCAACATGA | 57097 |
rs564113604 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3851821 | CTCAAGTGGGTCCCT[C/G]ACCCCCGTGTAGCTT | 57097 |
rs564160043 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3844142 | TAATTACCTAACGTC[C/T]GTGTAACTGCTGATT | 57097 |
rs564181385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3817288 | TTAGATATTATAAAT[A/G]AACTGTGGGTTAAAG | 57097 |
rs564225399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3833119 | AAATTTTAGTTTACT[A/G]CAACAAAGTATAATT | 57097 |
rs564227054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3840040 | CCTTTGGCTAGAAAG[A/G]TTCTTAAGTCACTCA | 57097 |
rs564253135 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3845802 | TCTCCCACTAATTGG[G/T]ATTATTTTTTAAAAG | 57097 |
rs564274863 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3843316 | TGTAGATGCTACGCA[C/G/T]TTTGAAAATAATCTG | 57097 |
rs564290136 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3852083 | AACAGAAAGGAATAG[C/T]ATCAACACCAACAAA | 57097 |
rs564322216 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PARP11 | GRCh38.p7 | 12:3846394 | CAACATGCCAACAAA[C/T]TGGAAAACTTAGAAG | 57097 |
rs564439072 | in-del | -/A | | | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3875137 | GCATCAGCATCTGTA[-/A]AAAAAAAAAAAAAAT | 57097 |
rs564537844 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3854501 | CATCAGAGAATACTA[C/T]GAACACCTCTACGCA | 57097 |
rs564557030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3873049 | GCACTTCCACTGCTT[A/G]AAAAGGTACAGACTA | 57097 |
rs564609093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3832269 | CCTTATCAAATTACA[C/T]TATTTTTTTCGTCCA | 57097 |
rs564700843 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PARP11 | GRCh38.p7 | 12:3811808 | TCCTGATAACACACA[C/T]GTAAACTTTAAAGAT | 57097 |
rs564787726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3823859 | AGGCGGAGGCTGCAG[C/T]GAGCCAAGATGGCAC | 57097 |
rs564812961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3828785 | TTATAGAGGTATTTT[C/T]GTATATAACAAAAAA | 57097 |
rs564825437 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PARP11 | GRCh38.p7 | 12:3816919 | AAAGAAGGCCAGGCG[C/T]AGAGGCTCACGCCTG | 57097 |
rs564866718 | snp | A/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3862763 | GGCCCTATTTTTTAT[A/T]CTATTCCATTCCATT | 57097 |
rs564884522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3841108 | CCTGTGTCAATACAG[A/G]CAGTTAACCAGCCCT | 57097 |
rs564910816 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3841479 | TGATGCCCACTTTCC[G/T]ATGCAGACTGAGGCT | 57097 |
rs565009089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3820942 | AACCATGAAAGAATT[C/T]CATGTATCATTACCA | 57097 |
rs565021841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3848098 | AATACATACGAGTCA[A/G]TTTAACTAAAATGAA | 57097 |
rs565127574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3870332 | TTTGGGTGGCAAAAG[A/G]AGAATGTGAGATGAT | 57097 |
rs565225831 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PARP11 | GRCh38.p7 | 12:3811937 | CAAGACTACAAGAAA[A/C]AGGCAAAAACAAAAC | 57097 |
rs565256895 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3827222 | CTGCAAAGAGTACAT[A/G]TGAAATGCTAATATC | 57097 |
rs565258554 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3859651 | CTAATCCAATCAAAA[C/T]GTAGATTTTTCAGAT | 57097 |
rs565296512 | snp | A/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3817003 | CAGACCATCCTAGCT[A/T]ACATGGTGAAACCCT | 57097 |
rs565306292 | snp | C/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3873970 | GAGCATATTTACCTA[C/G]AGTAGAGTGTCAGGA | 57097 |
rs565315520 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3874854 | TTTGAAGTGCCACTG[C/T]TAATTACAACCTAAA | 57097 |
rs565330829 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3847159 | GCAAACCAACAATAA[C/G]TAACAAGATTGAAGC | 57097 |
rs565345984 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | PARP11 | GRCh38.p7 | 12:3831104 | ATACAACTACTACAT[-/A]AAAAATATTCTTCTT | 57097 |
rs565418251 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3833748 | TCAGAACAAGTCAGA[C/G]TCTGTGGCGTTTGAG | 57097 |
rs565485292 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3853782 | GCTCTGCACCAAGCA[C/G]ACCTAATAGACATCT | 57097 |
rs565545905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3860343 | AGACAAGGAAGGACC[C/T]TAAAAGCAATTCAGA | 57097 |
rs565584046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3819990 | CTTCTCCTATCCAAC[C/T]GGTGTCTGGGGCTCC | 57097 |
rs565651703 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3871613 | AGGAGGCGCACGACT[C/G]TATTTAGTCCAACAA | 57097 |
rs565724317 | in-del | -/GTATGGT | | | intron-variant | PARP11 | GRCh38.p7 | 12:3850832 | ATATCTTACAGAAGA[-/GTATGGT]GTTGAAATGACCACT | 57097 |
rs565787510 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3852839 | TAATTGCCAGATTCA[A/C]CAAGGTTGAAATGAA | 57097 |
rs565814813 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3814343 | TCTAGAAAAGAAATA[A/C]TTTCAAATGTTCTTG | 57097 |
rs565848234 | snp | A/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3827307 | TATATGTAACTCCCA[A/T]TCCTTAATAATGATA | 57097 |
rs565928708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3842014 | ACACGAAAGGCAGAT[A/G]TGGCATTGGCTTCCA | 57097 |
rs565931985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3842654 | CTTCCCTCCCATACT[C/T]GACAAGACATTGTGG | 57097 |
rs565944979 | in-del | -/TAG | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3843891 | GCTATGCAAATAACA[-/TAG]TAGTAATTTCTCTTT | 57097 |
rs565945219 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3854586 | CCAAGACTAAACCAG[A/G]AAGAGGTTGAATCCC | 57097 |
rs566366222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839340 | CGACGGCGAGGACCA[A/G]GGCGGCGCGGGGCCC | 57097 |
rs566378038 | snp | A/G | | | intron-variant, nc-transcript-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3871719 | GGCAGTTTCAACCAT[A/G]ACAACAGAAGAATAC | 57097 |
rs566394468 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3873857 | CTATCCCTGCCCTCA[A/G]GATTTTATAATCTAG | 57097 |
rs566405461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3828496 | GAGGCTGCAGTGAGC[C/T]GAGATCATGCCACTG | 57097 |
rs566434114 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3832648 | ATAATTATGCTCAAA[C/G]AGTTAAGTCAAATTT | 57097 |
rs566453348 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839593 | CGCTTGGAAAATCCA[A/C]AGGAATGGGTAGGAC | 57097 |
rs566479686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3845062 | CACCATATTATGATC[A/G]TACATATTTTGAAGA | 57097 |
rs566483737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3824132 | GTTTTCCCACAACCA[C/T]TCCAAAAAGGTGTGT | 57097 |
rs566543228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3831923 | AAGGAAAGAAAGTGT[A/G]ACCTAAATTTAGTTT | 57097 |
rs566545197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3823482 | TATTCCTAGTGCTTA[C/T]GACAGAGCCTGGCAC | 57097 |
rs566596433 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3866959 | ATTGGACAAACTACC[C/T]GTGGAGAAAATATAA | 57097 |
rs566624163 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3872126 | AGGGACCTTCCTCCT[C/T]CGTAGGAGGAAGAAA | 57097 |
rs566655156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3831312 | AAACATATAGAGTTA[C/T]TGATGATTTGTTAAA | 57097 |
rs566733084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3851518 | ACTGCTAGCGCAGCA[A/G]TCCGAGATCAAACTG | 57097 |
rs566735074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3858570 | CTTGGTCCCTCAATC[A/G]CTTCTGATGTTTTAC | 57097 |
rs566777876 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3872647 | AAGAAGGGAAAAGGA[G/T]AACTGATGGCTCCTC | 57097 |
rs566798920 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PARP11 | GRCh38.p7 | 12:3857649 | TGCTAAAAAAAAAAA[A/G]GGAAAAGAAAAGGCA | 57097 |
rs566832942 | in-del | -/TCTT | | | intron-variant | PARP11 | GRCh38.p7 | 12:3816255 | TTCAATCTTCCAAGG[-/TCTT]TCTGACTGCTGATTC | 57097 |
rs566892077 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3821012 | ATGAGTTATGGTCTG[G/T]GATTTGCTTAAAAAT | 57097 |
rs566896167 | in-del | -/A | | | intron-variant | PARP11 | GRCh38.p7 | 12:3858339 | ATTAACCATGCAGAG[-/A]AAAGTGGCTGTAGAC | 57097 |
rs566920902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3872181 | ATCTGAACAAACAGA[C/T]CTTGCTGGGCTTCCT | 57097 |
rs567003990 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3820310 | ATATGGTGAGTCATA[C/G]GTTATGTGACAGTGA | 57097 |
rs567004224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3828372 | GTCAACATGATGAAA[C/T]GCTGTCTCTACTAAA | 57097 |
rs567066072 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3827761 | CCCCTTCACTGTTTC[G/T]GGGCCTTGGTTCATC | 57097 |
rs567120030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3812528 | CAGGAGAATAGATGC[A/G]TAGAATTGTATAATA | 57097 |
rs567124437 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3849297 | TATCCAGCAACTCCA[C/T]GACTGAGTATATACC | 57097 |
rs567343632 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3841748 | CACCTCCTTTCTTTC[C/T]TCATGTTTGGCATGG | 57097 |
rs567429931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3813850 | TATTCTTACCTATGA[C/T]TTTCTTAAAAACAAA | 57097 |
rs567664047 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PARP11 | GRCh38.p7 | 12:3846713 | AGTGAGCCAAGATTG[C/T]GCCACTGCACTCCAG | 57097 |
rs567676001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3853190 | AAAACATGCCAAACT[A/G]TAAAGACCATCGATG | 57097 |
rs567784043 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3834227 | GAGCAGTGGCATGGA[A/G]ACTTTGCTCAGGGGT | 57097 |
rs567817866 | in-del | -/A | 0.21303 | 0.247251 | intron-variant | PARP11 | GRCh38.p7 | 12:3834635 | GCGACACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 57097 |
rs567881494 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810124 | TTCAAATGATTCAAG[C/T]GAGCAATATAAGCAT | 57097 |
rs567886245 | snp | C/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3826587 | AGAGTACTAGAAAGA[C/G]AGAAATTACAGTATT | 57097 |
rs567894293 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3841144 | CCTTTGCCTCAGACA[C/T]TGAGCCTTTATCAAG | 57097 |
rs567995637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3847320 | TCAAACTCAATTCTA[C/T]GAGACAGCATTATCC | 57097 |
rs568032249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3856899 | TCCATCAATGATAGA[C/T]TGGATTAAGAAAATG | 57097 |
rs568062305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3843706 | GAGGTTCCCTTTGCA[C/T]GTTGTACTCTGTCCT | 57097 |
rs568285261 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3852486 | ACAAGAACTATGTGA[C/T]GCATGCACAAGCTTC | 57097 |
rs568344936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3872064 | CCATAAAGAAATTCT[C/T]TAATCTACCTTGCCT | 57097 |
rs568360638 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3830707 | CTAAGGACTACACAG[A/G]TGAAAATTCATTTAG | 57097 |
rs568423587 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3829522 | CCAAGTTACTGTGAG[C/G]ATAAGGGAGAAAATC | 57097 |
rs568434266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3870997 | AAGAGAGTATTATAC[A/G]TATGAATCGAAAATA | 57097 |
rs568648683 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839875 | GAACTAGACACGTTG[C/G]AAGTAGCTGATGAAG | 57097 |
rs568707021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3830319 | GTTTCAGCATAGCCC[C/T]AAGCATTTTCAATTT | 57097 |
rs568784082 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3833258 | AATGAACGAGAACTT[C/G]CAGAATGACAGAATA | 57097 |
rs568818870 | snp | C/T | 0.00517822 | 0.0506191 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3874491 | CTCGAACTCCTGACC[C/T]CAGGTGATCCACCTG | 57097 |
rs568938589 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | PARP11 | GRCh38.p7 | 12:3853315 | TAAATGAGCTAAATA[C/T]CCCAATTAAAAGACA | 57097 |
rs568988281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3817107 | GAGGCAGGAGAATGG[C/T]ATGAACCCCGGAGGC | 57097 |
rs568992465 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3825456 | AATGTAGGTGGAAAC[A/C]AAGTGAACAACTACC | 57097 |
rs569015499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3860570 | GATTTCATGGAACTT[A/G]CTCGGGACCTGTCAC | 57097 |
rs569038824 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PARP11 | GRCh38.p7 | 12:3811593 | ATTGTCTTGTTTCTG[A/T]TTTCTCTCAAGGTGC | 57097 |
rs569180494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3827059 | TACTGGATTTACCAC[C/T]GTTCAGGGAAAAAGC | 57097 |
rs569188933 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3870654 | TATTGAGTGCCTACT[A/G]TGTGTCAGGTTCTGT | 57097 |
rs569329810 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3864891 | TGTTGTTTTCTGTTG[G/T]AGTGATTTCCACTCT | 57097 |
rs569377824 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PARP11 | GRCh38.p7 | 12:3832454 | CCCCTAAGTTACCAA[A/G]CCCCACTGTCTCCTT | 57097 |
rs569388624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3813311 | CAATAGAATCCCATA[C/T]CCATGAAAAGATTTC | 57097 |
rs569396142 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3818466 | GAATCCATCAACTGC[A/C]CTTCCACTCTTTCTC | 57097 |
rs569421609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3851887 | ACCTCATACAGTCGG[A/G]TGCCCCTCTGAGACG | 57097 |
rs569443119 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3852223 | AAAACCAGAGCACCT[C/G]TTCTCCTCCAAAGGA | 57097 |
rs569502781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3859162 | GTAAAAGGCATATAT[A/G]AAACAAATAAATTCA | 57097 |
rs569504521 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3842545 | AAGTATTTTCTAACA[C/G]AAACTCTTAGGTGGA | 57097 |
rs569612516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3855669 | TGCTCATGGATAGGA[A/G]GAATCAATATCGTGA | 57097 |
rs569676150 | in-del | -/AGAG | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3855491 | CTACACACCAATAAC[-/AGAG]AGCCAAATCATGAGT | 57097 |
rs569722937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3870639 | AATTCAACAAATATT[C/T]ATTGAGTGCCTACTA | 57097 |
rs569754182 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PARP11 | GRCh38.p7 | 12:3849938 | CATGTCCTGAAAATA[C/T]GTATATCGATTATGT | 57097 |
rs569772132 | in-del | -/TTAG | | | intron-variant | PARP11 | GRCh38.p7 | 12:3829761 | TTTCTAACTTTTCTT[-/TTAG]TTAAACAATTTTATT | 57097 |
rs570006317 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | PARP11 | GRCh38.p7 | 12:3831511 | TCACAAAATGAAAAA[-/T]TGATAGACTCCTTCC | 57097 |
rs570058875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3861715 | CATCGATCATAGTCC[C/T]GGCATTGTAGCTAAA | 57097 |
rs570074188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3847420 | ATGCAAAAATCCTCA[A/G]TAAAATACTAGAAAA | 57097 |
rs570116276 | in-del | -/GCCGCCT | 0.0111196 | 0.0737302 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839161 | CCTCGGGCCGCCGCC[-/GCCGCCT]GCCGCCTGCCGCCTG | 57097 |
rs570193340 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3828384 | AAACGCTGTCTCTAC[C/T]AAAAATACAAAAAAA | 57097 |
rs570259041 | in-del | -/AAC | | | intron-variant | PARP11 | GRCh38.p7 | 12:3838517 | CTTCTAAAAAAAGAA[-/AAC]AACAATCTAACAATG | 57097 |
rs570268706 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3836339 | GTAAAAAACAAACAA[A/C]AAAAAAGCGCCTATC | 57097 |
rs570417683 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3820058 | GTTGGCAAAGGTGGA[C/T]GGGTCCCCTCACTTT | 57097 |
rs570420942 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3851466 | GATTATATCCCGCAC[A/C]TGGCTCAGCGGGTCC | 57097 |
rs570450796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3838715 | ATTCTTAGTCTTAGC[A/G]AGGCTAAGAAAAAAA | 57097 |
rs570504215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3825563 | GTTATTTTATGAGTT[C/T]AGAGCAGAGACCATA | 57097 |
rs570535851 | snp | C/T | | | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3874763 | TGGAAATAAAATAGT[C/T]TACTAAGAGATTATT | 57097 |
rs570602708 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3873365 | CGAAGGCCTTCCTCC[C/T]CCCCCTCCCTGTCAC | 57097 |
rs570639064 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3836705 | CAAAAACAAATACAC[A/C]GCACCAAGATTATCG | 57097 |
rs570717143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3831221 | GGGTTAGCCAATGCT[A/G]TAATTTCACTGCATA | 57097 |
rs570729478 | in-del | -/TTTTAAATATGTATTTAA | 0.0134861 | 0.0810011 | intron-variant | PARP11 | GRCh38.p7 | 12:3849961 | GATTATGTATCAACT[-/TTTTAAATATGTATTTAA]TTTTAAATATGTATT | 57097 |
rs570752774 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3864706 | ATAAAGTTGTTCATA[A/C]CATTCCTTTATTATC | 57097 |
rs570752910 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PARP11 | GRCh38.p7 | 12:3856971 | GGATGAGTTCAAGTC[C/T]TTTGCAGGGATATGG | 57097 |
rs570764815 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-5-prime | PARP11 | GRCh38.p7 | 12:3863938 | ATAGCACGGCTCAAA[A/G]ACTCGGGCATGCAAA | 57097 |
rs570775252 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3822647 | TGTGTGCTACTTTTT[A/T]GGTGTTCAATAGTGA | 57097 |
rs570786189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839258 | CCGGCGGCCTGGCCA[C/T]GTGGGGCTAGCCCTC | 57097 |
rs570852827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3871760 | TAGATCCCACTCTCT[A/G]AGGGTTGTGTTGGGG | 57097 |
rs570880055 | in-del | -/TTT | | | intron-variant | PARP11 | GRCh38.p7 | 12:3835924 | AAGTGCACCAACATA[-/TTT]TAAATAACTACAGTA | 57097 |
rs570924713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3834629 | ACAAGAGCGACACTC[C/T]ATCTCAAAAAAAAAA | 57097 |
rs571008786 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3809366 | TTATAAAAGAGGGGT[C/T]GGCAGTACATTCTCA | 57097 |
rs571027779 | snp | C/T | | | intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3872206 | CTTCCTTCCTCAGTT[C/T]ATTAACATTAGAGTA | 57097 |
rs571035377 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3834026 | AAAGGTAGAATTTCT[A/T]TTCCAGGTACAGCAG | 57097 |
rs571149593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3861343 | CAAAGTCCTCATAAA[C/T]GGCATTAAGGCTTTT | 57097 |
rs571149698 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3854104 | AGAACAAAGATACAA[C/T]GTACCAGAATCTCTG | 57097 |
rs571159483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3860695 | GACAGGGTCTTGCTC[C/T]GTTGTCTTGCACTTT | 57097 |
rs571180835 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3868108 | AAGTACTTTGTAAGA[A/C]GCTGCAAAAAAAAAA | 57097 |
rs571216035 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3863060 | AGAATGTTTTGTAGG[-/T]TTTCAATGTACAGAT | 57097 |
rs571241330 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3874508 | AGGTGATCCACCTGC[C/T]TTGGCCTCCCAAAGT | 57097 |
rs571289183 | in-del | -/TGTG | 0.00159617 | 0.0282053 | intron-variant | PARP11 | GRCh38.p7 | 12:3843453 | GGTTTCTAGAGTTAC[-/TGTG]TGTGTATTTTTTTTC | 57097 |
rs571331977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3847577 | AGAAGAAAAACCATA[C/T]AATCATTTTAATAGA | 57097 |
rs571512266 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839961 | TGCTGCTGCTGATGT[C/G]AATGGATTTAAACCT | 57097 |
rs571527710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3852313 | CAGAAGTTGGCTTCA[A/G]AAGGTTGGTAATAAC | 57097 |
rs571531624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3868931 | TACATGCATCTCAAT[A/G]GGCTAAAATCAAGGT | 57097 |
rs571551050 | snp | C/T | 1.64765e-05 | 0.00287019 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812255 | TTTGGAAGGAGGTCG[C/T]ATGTATTTGGAGTCT | 57097 |
rs571688790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3817742 | TGTATGCCACATGCT[C/T]TGCACTGGAGCAAGA | 57097 |
rs571689564 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3818497 | TAAGTCTTTTAAATT[C/G]TCCTTCTCCATAGGT | 57097 |
rs571703990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3835947 | CTACAGTATCAGAAG[C/T]GGAGGAGAGAGAAAA | 57097 |
rs571709166 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3859206 | GTACTATCTCCAAGA[C/T]ACATTATTATATAGA | 57097 |
rs571709499 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839532 | TCGAGAGAACAGAGA[C/G]AAATTTGAAGCGATT | 57097 |
rs571721593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3858714 | ATTTTGGTGATGCTA[C/T]TGCACTGCTTAGTTA | 57097 |
rs571721692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3866762 | AGGTAAAAATTCTTG[A/G]TACTGCTGAGAAGCT | 57097 |
rs571724176 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3873735 | TCAAAATGGAGATGG[C/T]AGTAATATCTCCCTA | 57097 |
rs571752058 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3826026 | GAGCCACTGCGCCTG[C/G]CCCAAGATTTGATAT | 57097 |
rs571841301 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PARP11 | GRCh38.p7 | 12:3813268 | ATTTCTATGATATGG[A/G]ATAACAATTCAGTAA | 57097 |
rs571903795 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3815619 | CAACAGTCCAGATAT[C/T]ATCAGACAGCACTGA | 57097 |
rs571965481 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3829396 | AAGACTACAGGTTTT[A/G]AGTGCGGATTCAAAT | 57097 |
rs571976152 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3836372 | CCAAGAATCTTATAC[A/T]AGCAAAACTATCTTT | 57097 |
rs571979827 | snp | C/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3864508 | CTTCCTTAAATATTT[C/G]GTAGAATTCACCACT | 57097 |
rs572016027 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3841903 | GTTTCCACAGTAGAT[G/T]AGTTTCCAGCAGCCA | 57097 |
rs572179702 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3823602 | TAATATTTAGCTTGC[C/T]TCCAACTTTTTGCTA | 57097 |
rs572288288 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3856226 | TGGGCAAGGACTTCA[C/T]GACTAAAACACCAAA | 57097 |
rs572415717 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3841274 | AGAATATTCTTCGAT[A/T]CTTCTTCAATCTTGG | 57097 |
rs572425350 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3874867 | TGTTAATTACAACCT[A/G]AATTTGCATATACAT | 57097 |
rs572462141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3827891 | AAGGACCAAGCTGTG[C/T]AGCAAACAAAATGTA | 57097 |
rs572507246 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PARP11 | GRCh38.p7 | 12:3813420 | ACTCGATAAAGCAGC[C/T]AACTCTTCTGAAATG | 57097 |
rs572539004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3834382 | TCATGCCTGTGATCC[C/T]AGCACTTTGGGAGGC | 57097 |
rs572568851 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3821451 | TTAGGCTAAGCAGGA[A/T]ATTTGAAGGTATGTT | 57097 |
rs572594944 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3822654 | TACTTTTTAGGTGTT[C/T]AATAGTGAACTTTTG | 57097 |
rs572612318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3870189 | ACTAACAAATTACTA[A/G]AGAAACCCACACGTA | 57097 |
rs572622203 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3864140 | TGCTGAGAATTTTAA[G/T]CAGGAATCGATATTC | 57097 |
rs572685073 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3840673 | ATCACACGTAAGTGA[C/T]AGAAAAGGAAGCAGG | 57097 |
rs572685304 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3867988 | ACACAAGTTGCAATT[C/T]CTGACAATCTATAAT | 57097 |
rs572722966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3869314 | CATATTTTCTAATAC[A/G]TAAACTCATTTTCCA | 57097 |
rs572727417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3820812 | TGTCAGAAATAAAAG[C/T]TGGTTTGGCCAATAG | 57097 |
rs572738042 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3840330 | AGTGTCAGGGAAGAA[G/T]ATGAAAAAACCTTCC | 57097 |
rs572826356 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3813685 | AAGGTACAAAGTAAG[A/G]ACCAGAAAATTAAAT | 57097 |
rs572834059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3824803 | TCATTTTTCTCCCAG[A/G]TTAAATACTTTCTGA | 57097 |
rs572928825 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3838853 | GGCGTGGGGAGCGCG[A/C]GGGGGACGCAGGCCC | 57097 |
rs572949722 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810262 | AGCTTTCTGAAAAAG[C/G]CTTGGTATACGTGCT | 57097 |
rs572951096 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3856565 | CCAAAACAAAACCAC[A/C]ATGAGATACCATCTC | 57097 |
rs572979886 | in-del | -/A | | | intron-variant | PARP11 | GRCh38.p7 | 12:3868114 | TTTGTAAGAAGCTGC[-/A]AAAAAAAAATCATCC | 57097 |
rs573009082 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3867243 | TCCTGATTATAACTG[-/A]AGTGTTGAAGGAAAT | 57097 |
rs573042340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3858737 | CTTAGTTATCCTGAA[C/T]ACATTATTTTTTCAC | 57097 |
rs573042467 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3811430 | TAGGCTAATGACATT[C/T]TGCAGCAATTATCAA | 57097 |
rs573061734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3851993 | TACCCAGGCAAACAG[A/G]TTCTGGAGTGGACCT | 57097 |
rs573075908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3865263 | GATATGTTTTATGGG[C/T]CAGAATATGGCATAT | 57097 |
rs573120049 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | PARP11 | GRCh38.p7 | 12:3851676 | AGACTCCACCTCTGG[C/G]GGCAGGGCATAGCTG | 57097 |
rs573176297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3815438 | CACAAAACAACATTG[C/T]AAATTTGAACACCTA | 57097 |
rs573272191 | in-del | -/A | 0.417196 | 0.185864 | intron-variant | PARP11 | GRCh38.p7 | 12:3859560 | GAGTGAGACTCTGCT[-/A]AAAAAAAAAAAAAAA | 57097 |
rs573279903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3871794 | AGAAAATACTACCCC[A/G]AAGTATGACACTTTG | 57097 |
rs573284550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3854162 | GAAATTTACAGCACT[A/G]AATGCCCACAAGAGA | 57097 |
rs573286261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3822884 | CTCCTCAACCATTCA[C/T]TCGATGTTCTCCAAG | 57097 |
rs573346103 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PARP11 | GRCh38.p7 | 12:3853683 | TCCCACACAATAACA[A/G]TGGGAGACTTTAACA | 57097 |
rs573353285 | snp | C/T | 0 | 0 | intron-variant | PARP11 | GRCh38.p7 | 12:3838002 | GCAATACAGCAAAAG[C/T]AAGAAACTTAAAAAA | 57097 |
rs573447640 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3819803 | AAGACGATCACACAA[C/T]CACCCCAGTGGTGCT | 57097 |
rs573661609 | snp | C/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PARP11 | GRCh38.p7 | 12:3811789 | TTTAAACTAAAATCA[C/T]TTATCCTGATAACAC | 57097 |
rs573852986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3827114 | AGACCTGTGATGCCA[C/T]CTTCTTGGACCATCT | 57097 |
rs573918649 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PARP11 | GRCh38.p7 | 12:3826460 | GACGTAAGCTCACAC[A/G]TAAAGATGCTCATTT | 57097 |
rs573958516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839406 | GAAACTGGGCTTGTA[C/T]CGGAAACTGGTCGCC | 57097 |
rs574027887 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3834463 | CATGGTGAAACCCCA[A/G]CTCTACAAAAAATAC | 57097 |
rs574183753 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3867384 | GCTGTCAAGGAAAAA[A/C]GGTGCTGACAAGTTT | 57097 |
rs574306914 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3833507 | CCCTTGAGAGGCTGA[A/G]ATGGAAGGATTACTT | 57097 |
rs574315774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3822953 | ACTATTCTCTCCAAC[A/G]GTCCACTACCTTTAA | 57097 |
rs574325692 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3874570 | CCGGCCATATTTTAA[A/G]GTAGACTCATGGCAT | 57097 |
rs574384724 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PARP11 | GRCh38.p7 | 12:3836498 | TTTATCAGGCTGAAA[C/T]GATACTAGGCATTCG | 57097 |
rs574398540 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3845731 | CTAATAATGTCTCAT[G/T]TCCAATATGTTATTT | 57097 |
rs574456827 | in-del | -/A | 0.48818 | 0.0759629 | intron-variant | PARP11 | GRCh38.p7 | 12:3822599 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 57097 |
rs574485597 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3848323 | AATCCTAAAATTTAT[A/G]TAGAACCACAAAAGA | 57097 |
rs574497114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3842966 | CAAATAGAAATGTCT[A/G]TTTTATTATGCAATG | 57097 |
rs574558498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3842359 | TATTCTGGTAGGGGC[A/G]GATATCAACATGTGA | 57097 |
rs574606202 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3863606 | GTGAAAGAACATAGA[A/G]TAAAATCAGCAAAGG | 57097 |
rs574677862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3830642 | AAGTGTCAGGATACA[A/G]TAACAATAATAGTAA | 57097 |
rs574729912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3872263 | ACAGTTGTCTATTCT[C/T]CATGGGTCCTACGCA | 57097 |
rs574776545 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3871826 | CATGCTGAATACTTT[C/G]AACTAAAAGAGATTG | 57097 |
rs574844623 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3821598 | CAACAAAGCTAAACA[A/G]CTCTGACACTCCTCT | 57097 |
rs574906277 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3828531 | CCAGCCTGGGCAACA[C/T]AGTGAGACGTCTCAA | 57097 |
rs574977709 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3873446 | CCAGTCAGATCTGTC[C/T]CCGCCCCACTCCTAC | 57097 |
rs574980125 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3855811 | AAAAAAGAGCCCACA[G/T]TGCCAAGACAATCCT | 57097 |
rs574982354 | in-del | -/TTC | | | intron-variant | PARP11 | GRCh38.p7 | 12:3824829 | TCTGAAGATAAGTAA[-/TTC]TTTTATTATATTATT | 57097 |
rs575010568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3814455 | CCATGCTATGCCCCA[A/G]TATCATAAAGGTAAT | 57097 |
rs575070469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3849552 | AAAATAAGCCAAGCA[C/T]GGAAAGACAAATATC | 57097 |
rs575097590 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3861810 | CGGGCGGATCACGAG[A/G]TCAGGAGATTGAGAC | 57097 |
rs575118292 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3813573 | ACAGTTAAATAAGTG[C/G]AATGGCCTTTTTAGT | 57097 |
rs575185406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3867107 | TTTGTGAGCTATGAC[A/G]TAAGTTGAAAAAGGT | 57097 |
rs575212594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3844095 | GAATCGCCACTGTAC[C/T]GTAATAATGGTTATT | 57097 |
rs575385401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3862609 | TTTTATATACTATAT[A/G]TATAATTTTTATAGT | 57097 |
rs575431072 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839358 | CGGCGCGGGGCCCCG[A/C]GAGGACGCGACGCCC | 57097 |
rs575436553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3852505 | TGCACAAGCTTCAGT[A/G]GCTGATTCAATCAAG | 57097 |
rs575448731 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3837157 | CATTGTAGGAGCTTC[A/G]CTCCACAGGTTTCCC | 57097 |
rs575451015 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3859361 | CAAGGTCAGGAGATC[A/G]AGACCAACTTGACCA | 57097 |
rs575464806 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3858894 | CAGGAGTTCAAGACC[A/G]GCCTGGCCAACATGG | 57097 |
rs575490070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3846331 | AAATGAAAAAGGTGA[C/T]AACTGAGACCACAAG | 57097 |
rs575604678 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3857128 | ACCAGGGCCTGTCGG[C/G]GGGTGGGGGGCTGGG | 57097 |
rs575657548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3818659 | AACATTTGCTGTATA[C/T]ACAATATGATGTCTA | 57097 |
rs575688066 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810829 | AAGAAGAGAAGAGAA[A/G]GAGGAGAGAAGAGAA | 57097 |
rs575709403 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3835734 | TTCTGGAGTTGAAAA[A/G]TATAGTAAGTAAAAT | 57097 |
rs575769693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3812652 | ATAGATTTGTTGGTA[C/T]AGACCAGTCCTCACC | 57097 |
rs575927828 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3848917 | ATGTGACAATGGATT[A/C]ATAATAATAATATAT | 57097 |
rs575946979 | in-del | -/C | 0.00557542 | 0.0525036 | intron-variant | PARP11 | GRCh38.p7 | 12:3858502 | TGACTCTAAAGGAAA[-/C]ATTTTTAAAAGCCAT | 57097 |
rs576082923 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3824218 | TTGTTTTTCTCCTAT[C/T]ATGAGTGAGGTTGTA | 57097 |
rs576191431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3820387 | CGCTGCCCTTATAAT[A/G]AGACTCAGTATTTTG | 57097 |
rs576191476 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PARP11 | GRCh38.p7 | 12:3811821 | CACGTAAACTTTAAA[C/G]ATCTCAATGACCACA | 57097 |
rs576241986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3819921 | GCTTCAATTTTCTGC[A/G]CTCCCTCTTATATCC | 57097 |
rs576362340 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3833624 | AATTAATTAAAAATT[A/T]AAAACTGCTGAAAAT | 57097 |
rs576472529 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3859335 | TTTGCGAGGCCGAGG[C/T]GAGTGGATCACAAGG | 57097 |
rs576495212 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3831775 | CCACTATTTACCTTA[C/T]ATATTTTAACCACAT | 57097 |
rs576569996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3840016 | AACAATGGGAACTCT[A/G]CTAGCCTGCCTTTGG | 57097 |
rs576589283 | snp | A/G | 0.0023933 | 0.0345097 | downstream-variant-500B | PARP11 | GRCh38.p7 | 12:3808426 | TGCCAAAGGTTGAAC[A/G]GAATGTTTAACTCAG | 57097 |
rs576621381 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3820483 | TCATTACATAAAACC[A/G]TGAAGGGCATCACCA | 57097 |
rs576650565 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PARP11 | GRCh38.p7 | 12:3816468 | AATACCCACCAGCAC[A/G]TATTTCTCCATCTTG | 57097 |
rs576699394 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3827162 | TTCACCATTTTTATA[C/G]AGAAAACCTGAGTTG | 57097 |
rs576752898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3831539 | TCCTCATTGGGATGT[C/T]GTTATAAATGAATGA | 57097 |
rs576836028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3843795 | AAATAACTGTAGCTT[A/G]TATTCCTTATTTGTA | 57097 |
rs576853790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3862513 | ATTTGTAGTCTTAGA[C/T]TCTGCATTTAGGTCT | 57097 |
rs576976557 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3837054 | GACAAAGGAGTCAAG[C/T]AGGACTACAATCCCT | 57097 |
rs577022117 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3849285 | GAACTACCATATTAT[C/T]CAGCAACTCCACGAC | 57097 |
rs577086258 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3872639 | TGTCCACCAAGAAGG[C/G]AAAAGGAGAACTGAT | 57097 |
rs577086807 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | PARP11, LOC105369609 | GRCh38.p7 | 12:3872364 | TTACCTTGTTAACCT[A/C]TCTTCTGTTTTAAGG | 57097 |
rs577090830 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3823642 | GAAAGCTGGCTGGGC[A/G]CGGTGGCTCATGCCT | 57097 |
rs577136596 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PARP11 | GRCh38.p7 | 12:3857242 | GAAACAAACCTGTAC[A/G]TTGTGCACATGTACC | 57097 |
rs577182083 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PARP11 | GRCh38.p7 | 12:3822327 | CTGTCGGCCGGGCGC[A/G]GTGGCTCACGCCTGT | 57097 |
rs577199372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3864319 | TCCTTTTATATATGT[C/T]AGATTTGAGTTGCTA | 57097 |
rs577244202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3859380 | CCAACTTGACCAACA[C/T]GGTGAAACCCTGTCT | 57097 |
rs577292489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3829592 | GTTTAATACGGATTT[A/G]TTCTTCCCTTTCTCT | 57097 |
rs577293208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3821677 | GGAGCTTCTCACATT[A/G]CAATGCTACAAGCAA | 57097 |
rs577417985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3849660 | CTGGGAAGGGCAGGG[A/G]GAGAGACTGATTAAA | 57097 |
rs577478693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3855881 | ATTTCAAACTATACT[A/G]AAAGGCTACAGTAAC | 57097 |
rs577530079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3860028 | AGAACGCAAGAAGAG[A/G]GAATGACTTAAAGAC | 57097 |
rs577530303 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PARP11 | GRCh38.p7 | 12:3852682 | TGAAAGTGACGGGGC[A/G]AATGGAACCAAGCTA | 57097 |
rs577582159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3818703 | CATCTAAGTTACCAA[C/T]GGCCTTCTTATTGAA | 57097 |
rs577595066 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3838923 | GGGCTTTTCTCGCTT[A/C]ACACCGGTACAGACG | 57097 |
rs577662232 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3815218 | CGGCTTCTGATAGCT[A/C]TTTAATGCCTGCTTC | 57097 |
rs577672539 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3811126 | GTCAACAGCTACTTC[A/C]AAGGAGAAACCAGAT | 57097 |
rs577689488 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3866376 | TGGCTCAGTCCTAGC[A/C]CTTCTTGTTTTCTCT | 57097 |
rs577693616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3818094 | CTGAAGTACATTACA[C/T]AACATGGTTTGCCCT | 57097 |
rs577696257 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PARP11 | GRCh38.p7 | 12:3826383 | TATGGGTACTTTACC[A/G]TGCAGCTAGCTATGT | 57097 |
rs577746341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3840755 | AGTTGGATAAAAGAC[C/T]CGAACCAAGCATATT | 57097 |
rs577808048 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3846929 | GTCTCTGCACAAAAT[G/T]TAAAAATTAGCTGGG | 57097 |
rs577813360 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3846419 | TAGAAGAAATGGATA[A/C]ATTCCTGGACATATA | 57097 |
rs577821763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3833009 | CTGAATCATCAAATT[A/G]AAAAGCTGTGTGGAA | 57097 |
rs577883353 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839375 | AGGACGCGACGCCCA[G/T]GGACGCCTATCTGCG | 57097 |
rs577946328 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PARP11 | GRCh38.p7 | 12:3845432 | TAAAATGCCTGTGAA[C/G]TGCAAACTTGCTTAT | 57097 |
rs577998841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PARP11 | GRCh38.p7 | 12:3851945 | AATATTTGCTGTTCT[A/G]CAATATTTGCTGTTC | 57097 |
rs578033029 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PARP11 | GRCh38.p7 | 12:3811751 | GTCTGTATTTTTTTT[C/T]AACATTTATACGAAT | 57097 |
rs578055886 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3836804 | AAACTCTGAGCAGAC[A/G]GTAACGGAATTGGAT | 57097 |
rs578137579 | snp | C/G | 0.0130921 | 0.0798413 | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3873494 | GCACGCTTATCCATA[C/G]GCGCGCGGGCGGTCG | 57097 |
rs745349560 | snp | A/G | 6.67456e-05 | 0.00577654 | synonymous-codon, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3826214 | CTGCTTTCCAGTGGT[A/G]AGATTCATTTGCTTC | 57097 |
rs745361704 | snp | C/T | | | intron-variant, nc-transcript-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3871839 | TTGAACTAAAAGAGA[C/T]TGGAAGGCCTCAGAA | 57097 |
rs745394561 | snp | A/G | | | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3873483 | GCCCCGCCCCTGCAC[A/G]CTTATCCATACGCGC | 57097 |
rs745425871 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3823713 | CTGAGCTTAGGAGTT[C/T]GAGACCAGCCTGGGC | 57097 |
rs745437891 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3837423 | GTTTGTAAGTCTTGC[A/G]GTAACCATAATGCAA | 57097 |
rs745687336 | snp | C/G | | | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3840494 | GTCATTCTTCAGGGT[C/G]ACAGTCTCAGAAATT | 57097 |
rs745728384 | snp | A/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3831888 | CATTTCATTGGGCCA[A/T]TTAACTGTGAGAAAG | 57097 |
rs745729863 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3825296 | TTCAGACTTCTTATG[A/G]CCAGAGCAAGCAAAA | 57097 |
rs745738053 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3809250 | GTACTGATTATATGA[C/T]TCTCGATTTAATCTA | 57097 |
rs745774319 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3859790 | ACAGTCATAAAAAAG[A/C]TGGAGTGGCTATACT | 57097 |
rs745826050 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810136 | AAGTGAGCAATATAA[G/T]CATAGACACTGGAAT | 57097 |
rs745836129 | in-del | -/C | 1.64768e-05 | 0.00287021 | frameshift-variant, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812233 | TAAATTCACATAGCT[-/C]CCCGTCTTTGGAAGG | 57097 |
rs745861309 | snp | A/G | 5.19809e-05 | 0.00509782 | intron-variant | PARP11 | GRCh38.p7 | 12:3826285 | AGTACACTGTACTAT[A/G]AAGTGTCATGAAGAT | 57097 |
rs745912613 | in-del | -/T | | | intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3871999 | CTACAAAGCAAGCCA[-/T]TAAAAACTGGAACTA | 57097 |
rs745922688 | snp | A/G | 1.64933e-05 | 0.00287165 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3822003 | TGTGCAGAGGAATAA[A/G]CTGGAAAAATAAATT | 57097 |
rs745925977 | snp | C/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3867555 | CTACTACTTCAGGGC[C/G]AAAATACCCTGATTT | 57097 |
rs745944547 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3853408 | TCACGTGCAGAGACA[C/T]ACACAGGCTCCAAAT | 57097 |
rs745974844 | snp | C/T | 1.65037e-05 | 0.00287256 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3821921 | ATTCTCTGAATTCTT[C/T]TAATTCGGTTGCGAT | 57097 |
rs746041057 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3817897 | CAGTAGATCTGTGGC[A/G]GGTGACAGGTATCTC | 57097 |
rs746186216 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3827531 | TAAAAATGCCTACCA[A/G]ATACCTTCTGCCTAG | 57097 |
rs746211849 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3841258 | GACCTACCTAAAGAT[A/G]AGAATATTCTTCGAT | 57097 |
rs746211995 | snp | C/G | 1.64825e-05 | 0.00287071 | synonymous-codon, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812195 | GATCTTTGGGTTCCA[C/G]GTATCATCCACACAG | 57097 |
rs746228098 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3820393 | CCTTATAATGAGACT[C/T]AGTATTTTGTACTGT | 57097 |
rs746254129 | snp | A/G | 4.94482e-05 | 0.00497209 | intron-variant, missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3829029 | TGACTGTTGGTATCC[A/G]GCTTTAAGACAAACC | 57097 |
rs746254817 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3858554 | CCTATAGGAGCCACT[A/G]CTTGGTCCCTCAATC | 57097 |
rs746299830 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3828855 | ACCTTCAGAGCTGTA[G/T]ATTTTATCATATCAA | 57097 |
rs746323792 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3854869 | CCTGATGAACATCAA[C/T]GCAAAAATCCTCAAT | 57097 |
rs746537281 | snp | A/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3854997 | GCAAATCAATAAACG[A/T]AATCCATCACATAAA | 57097 |
rs746593808 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3850959 | ACATAAAGCTAAAAA[A/C]AAAATCTTGTTCATG | 57097 |
rs746598848 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3813797 | CAACATTATAAATAA[C/T]GTGAAGTTTTCCCCC | 57097 |
rs746688821 | snp | C/G | | | intron-variant, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3815011 | AATCTCAGGAGGAAA[C/G]AAGGAGAGTAGGACA | 57097 |
rs746721195 | snp | C/T | | | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3840999 | TGGACCAACAGGTGT[C/T]CCTGCTCCAATTCCT | 57097 |
rs746746559 | snp | C/T | 6.59859e-05 | 0.00574357 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3821933 | CTTTTAATTCGGTTG[C/T]GATCCATCGTCTTCC | 57097 |
rs746830260 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3809054 | GCTGATATCACCAAG[C/G]TGAAAAAGAAAAGTC | 57097 |
rs746848397 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3842686 | CATGAGTTCAAGGGG[G/T]CAGGTTAATTCCTGG | 57097 |
rs746885632 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3836024 | AATTTTATATATATA[C/T]ACACACACACATATA | 57097 |
rs746906596 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3821553 | GTTTGCAGAGACTTC[C/T]AATAAAAGGCTTAGC | 57097 |
rs746907722 | in-del | -/CT | | | intron-variant | PARP11 | GRCh38.p7 | 12:3842549 | ATTTTCTAACAGAAA[-/CT]CTTAGGTGGAATGTT | 57097 |
rs747008753 | snp | A/T | 1.65605e-05 | 0.0028775 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812152 | TCAAGTACTCAGGAT[A/T]GATTTGGTTGGCATC | 57097 |
rs747067013 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3866206 | TCTTACTTATCTCAC[A/G]GTAACATTTCACAGT | 57097 |
rs747079190 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3831695 | TTCTTCATGTTTTAA[A/G]TTTGGTTGGCTTCTA | 57097 |
rs747099543 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3864887 | TCACTGTTGTTTTCT[A/G]TTGTAGTGATTTCCA | 57097 |
rs747116256 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3832290 | TTTTCGTCCACAATC[C/T]AATGTGCAGGAGAGA | 57097 |
rs747145338 | in-del | -/A | 1.67565e-05 | 0.00289447 | intron-variant | PARP11 | GRCh38.p7 | 12:3814031 | ACCTGGAATTCTGAT[-/A]ATTACCTTTTCCAAA | 57097 |
rs747190690 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3823566 | AGACGCACAGAACTC[C/T]GCCATGTGGATACAC | 57097 |
rs747197708 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3844114 | ATAATGGTTATTTAC[C/T]TCTGTGCTGTTTTAA | 57097 |
rs747199533 | snp | C/T | 1.64868e-05 | 0.00287109 | intron-variant | PARP11 | GRCh38.p7 | 12:3822027 | ATAAATTTGCATAGA[C/T]TTACTGCAGTCATTT | 57097 |
rs747252921 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810057 | CTTTAAGAATTACTA[G/T]CCCTAATCTGTCTGC | 57097 |
rs747349892 | snp | G/T | 1.79838e-05 | 0.0029986 | intron-variant | PARP11 | GRCh38.p7 | 12:3812472 | AAGAAAAGCCAAGAT[G/T]ACTCCGAAGAATATA | 57097 |
rs747406907 | snp | A/G | 1.64768e-05 | 0.00287021 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812320 | GAAACATAGATTTAT[A/G]TGTTCTAAACAGATG | 57097 |
rs747414834 | snp | C/G | 1.64749e-05 | 0.00287005 | utr-variant-5-prime, missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3829934 | CCAAGTAAAACCAGC[C/G]CCACTGGGTATCTGA | 57097 |
rs747424563 | snp | A/G | 1.65861e-05 | 0.00287972 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3830007 | TAATTCTTCTGCTTT[A/G]TGAAACATCTCCTGA | 57097 |
rs747480896 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3811102 | TCTAACTTTTCAAGA[C/G]AGTAGGTTGTCAACA | 57097 |
rs747580078 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3858041 | ACTGAAGACATAGTC[A/G]TGCCTGACACAACCT | 57097 |
rs747643710 | snp | A/C | 3.29832e-05 | 0.00406085 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812178 | GCATCAAAAACCACA[A/C]AGATCTTTGGGTTCC | 57097 |
rs747671113 | snp | C/T | 3.29506e-05 | 0.00405884 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812278 | TGGAGTCTCCGTTTA[C/T]GTAATCTCCAATTAG | 57097 |
rs747720936 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3862952 | GCATTGAATTATCAA[C/T]CTGTCTGGAGAAAAT | 57097 |
rs747727487 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3848156 | GCTTATGAAAGAAAT[C/T]AAAGACATAAAAATG | 57097 |
rs747732561 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3827435 | CAAATGCTTTGATAC[A/G]GTTCATCCTCTACAT | 57097 |
rs747777856 | snp | C/T | 1.64776e-05 | 0.00287028 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812236 | AATTCACATAGCTCC[C/T]GTCTTTGGAAGGAGG | 57097 |
rs747926578 | snp | C/T | | | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3870233 | TAAAACCAAATTGCG[C/T]TTACTGATATCATTC | 57097 |
rs747943405 | snp | C/T | | | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3871327 | GCTTTCAGTCAACCA[C/T]GGATCGCATATACAA | 57097 |
rs747952866 | in-del | -/TAA | | | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3874935 | AACATTCTCCTCTAT[-/TAA]TTATCTGCTTATTCC | 57097 |
rs747954256 | in-del | -/GG | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810622 | AAAAAGAAAAAGGGA[-/GG]AGGGAGGGAGGGAGG | 57097 |
rs747968396 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3822400 | TCAGGAGATCGAGAC[C/T]ATCCTGGCTAACACG | 57097 |
rs747979340 | snp | C/T | 1.64811e-05 | 0.00287059 | intron-variant | PARP11 | GRCh38.p7 | 12:3822049 | CAGTCATTTCCGGTT[C/T]CTTTCATGGGTATAT | 57097 |
rs748061768 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3833390 | AGGTTTGCATGAGGC[C/T]AGGAGTTTGAGGCAA | 57097 |
rs748206742 | in-del | -/TGTT | | | intron-variant | PARP11 | GRCh38.p7 | 12:3864927 | TTATTTCCTTGCTCC[-/TGTT]TAACTTCTTCTTTTT | 57097 |
rs748247434 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3823774 | ACAAAAAAGTAGCCA[A/G]GCATGGTGGCGTGCG | 57097 |
rs748300054 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3830313 | CTTCAGGTTTCAGCA[C/T]AGCCCCAAGCATTTT | 57097 |
rs748341917 | in-del | -/A | 1.83724e-05 | 0.00303082 | intron-variant | PARP11 | GRCh38.p7 | 12:3814237 | ACAGAAATATACCAT[-/A]AGTAGCATTTATTAA | 57097 |
rs748381258 | snp | A/G | | | downstream-variant-500B | PARP11 | GRCh38.p7 | 12:3808800 | AGGTTTAAATAATAC[A/G]AGGTGGAGATGAGAT | 57097 |
rs748515338 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3866592 | CTCTCTGTTGATACA[C/T]TCATATCAGCCATAG | 57097 |
rs748542647 | in-del | -/AG | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810753 | GGAAGAGAAAAAGGA[-/AG]AGAGAGAAAGAGGAA | 57097 |
rs748576855 | snp | A/C | 1.64863e-05 | 0.00287104 | synonymous-codon, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3814122 | AAATTCACTGCTGGT[A/C]CCATGAAACAGCATT | 57097 |
rs748596574 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3815262 | TCAAGTACTCACAGC[A/G]TCACGTGCTCACTTT | 57097 |
rs748600853 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3831485 | TGCCTTGTCTAGGCC[A/G]CAGTTGGCTCTTCAC | 57097 |
rs748796233 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810473 | TATGCACCTGTAGTC[C/T]CAGTAACTGGAGAAG | 57097 |
rs748840668 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810946 | CCTATGCAACATGCC[C/T]GCCAAGTTGCTGTCT | 57097 |
rs748885865 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3837585 | AAAATGAACTAGTAA[A/G]GACGACTTTATAAAT | 57097 |
rs748927276 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3825459 | GTAGGTGGAAACAAA[A/G]TGAACAACTACCTAA | 57097 |
rs748949914 | snp | A/C | 1.64757e-05 | 0.00287012 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812298 | TCTCCAATTAGCACT[A/C]GAGCAAGAAACATAG | 57097 |
rs748987171 | snp | C/G | | | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3873533 | GGGGCTTGCGAGTCT[C/G]TGTCTGACGAAGGAG | 57097 |
rs749059695 | snp | C/T | | | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839473 | CAGGTATTGCACTCT[C/T]AGTCTCGCCATGTTG | 57097 |
rs749068267 | snp | C/T | 1.66385e-05 | 0.00288426 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3826192 | AGGGGGCTCTTTTTA[C/T]TAAGCGCTGCTTTCC | 57097 |
rs749144201 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3833273 | CCAGAATGACAGAAT[A/C]AGGAGCTCAGTGGAA | 57097 |
rs749147550 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3824531 | TCCCACAGTAAATAA[A/G]TATTTCTATATCAGC | 57097 |
rs749183855 | in-del | -/AGAAG | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810646 | GAGGGAGGGAGGGAA[-/AGAAG]GAAGGAAGGAAGGAA | 57097 |
rs749190029 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3861633 | ATCTTTTCATTCTCC[G/T]AGAAGCATGTTTTCA | 57097 |
rs749243412 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PARP11 | GRCh38.p7 | 12:3811616 | CAAGGTGCTCAGACT[A/G]TTTCAGAGTTTTAAA | 57097 |
rs749249224 | in-del | -/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3855437 | ACTTCAGCAAAGTCT[-/C]CAGGATACAAAATCA | 57097 |
rs749334415 | snp | C/G | 1.65941e-05 | 0.00288041 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3814170 | CACACCTCTTTTTTT[C/G]TTGAGCTGAGCCTTT | 57097 |
rs749404761 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3841267 | AAAGATAAGAATATT[C/T]TTCGATTCTTCTTCA | 57097 |
rs749448493 | snp | A/G | 8.82698e-05 | 0.00664282 | intron-variant | PARP11 | GRCh38.p7 | 12:3830066 | AATTCTATTAATAAC[A/G]AGTATACTTTTTACA | 57097 |
rs749480838 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3853700 | GGGAGACTTTAACAC[A/C]CCACTGTCAATATTA | 57097 |
rs749485794 | snp | A/G | | | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3870011 | CCCAGGCAGGATGGA[A/G]CACAATGGCATGAGA | 57097 |
rs749604600 | snp | C/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3816138 | TCAGAACTTTATGTT[C/G]TCACTTTTTTTAAAC | 57097 |
rs749660542 | snp | A/T | 1.67722e-05 | 0.00289583 | intron-variant | PARP11 | GRCh38.p7 | 12:3828873 | TTTATCATATCAATA[A/T]ACTAAAAACACACAA | 57097 |
rs749696850 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3829144 | CGAGGGAAACTTACT[A/C]ATCACCTGTTCTAGT | 57097 |
rs749754397 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3856178 | TAAAAACTCTAGAAG[A/G]AAACCTAGGTAATAC | 57097 |
rs749757635 | snp | A/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3842317 | AATCAAACTTATGGG[A/T]GCAGGAAGTACAAAA | 57097 |
rs749836381 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3830101 | ATTTTACTTCTTTAC[A/G]AAGAGTGGTATTCAA | 57097 |
rs749859373 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3819006 | CCCCACATTTTCTAA[C/T]AACTCCAAAACCTTT | 57097 |
rs749904011 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3867034 | ACAACTTTTTGTTCT[A/G]CATATCAGTGAAAAC | 57097 |
rs749961520 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3852290 | GGAGAATGACTTTGA[C/T]GAGTTGACAGAAGTT | 57097 |
rs749961911 | snp | C/T | 0.000162272 | 0.00900608 | intron-variant, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3815036 | AGGACAGGGATGGAG[C/T]AAACACTTCACCTGT | 57097 |
rs750028533 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3865606 | ATTAAGAAATGACAT[C/T]CTTTATCCTTGATAA | 57097 |
rs750037061 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3816399 | AAGAGAGCATGCATG[C/T]CTTTCGAGTTACTCT | 57097 |
rs750214060 | snp | C/T | 1.68301e-05 | 0.00290082 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812134 | GAAATCAATGAAAGT[C/T]TATCAAGTACTCAGG | 57097 |
rs750251942 | snp | A/G | 3.29533e-05 | 0.00405901 | intron-variant, synonymous-codon, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3828965 | AGAAATGGAGCCACA[A/G]GGGTTTGTTTTGAAG | 57097 |
rs750285995 | snp | A/G | | | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3874282 | TTTATTTATTTAGGC[A/G]GAACCTCGCTCTGTC | 57097 |
rs750293593 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3856995 | GATATGGATGAAGCT[G/T]GAAACCATCATTCTG | 57097 |
rs750297073 | in-del | -/A | 1.64756e-05 | 0.00287011 | intron-variant, frameshift-variant, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3828990 | TTGAAGCTTTTTTCG[-/A]TATCTTCACTGCTAA | 57097 |
rs750413536 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3826396 | CCATGCAGCTAGCTA[G/T]GTACCACGTTGTGGA | 57097 |
rs750532522 | snp | A/G | | | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3869623 | CTTTACCTGGCTAAC[A/G]CTTGCTCAATCCTTC | 57097 |
rs750553139 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3862397 | TCAATGTTACAATGA[A/G]CTATGATCACACCAC | 57097 |
rs750582555 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3847491 | CAAGTGGGATTCACA[C/T]CCCAAGGATGCAAGG | 57097 |
rs750746907 | in-del | -/CT | | | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839469 | GGAGCAGGTATTGCA[-/CT]CTCAGTCTCGCCATG | 57097 |
rs750760819 | snp | C/T | 1.74336e-05 | 0.00295237 | intron-variant | PARP11 | GRCh38.p7 | 12:3826124 | GTAAGAAAAAAAAAA[C/T]CCACTCTTTCCACCC | 57097 |
rs750809427 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3828857 | CTTCAGAGCTGTAGA[C/T]TTTATCATATCAATA | 57097 |
rs750873754 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3858998 | GTTACTTGGGAGGCT[A/G]AGGCAGGAGGATCAT | 57097 |
rs750908667 | snp | A/C | | | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3870975 | TACTTTCCTCTAATG[A/C]AGCTTGAAGAGAGTA | 57097 |
rs750940110 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3820784 | CTGTCTAAACTCAGT[G/T]AAACTCAGTTATTGT | 57097 |
rs750995549 | in-del | -/A | | | intron-variant | PARP11 | GRCh38.p7 | 12:3859098 | GCAAGACTCCATCTC[-/A]AAAAAAAAAAAAAGA | 57097 |
rs751003046 | snp | A/G | 1.64746e-05 | 0.00287002 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3822123 | CATTCTCCCAGTGTG[A/G]TGGCATAGGGATGGC | 57097 |
rs751025190 | in-del | -/A | | | intron-variant | PARP11 | GRCh38.p7 | 12:3859804 | CTGGAGTGGCTATAC[-/A]TAATGCCAGGCAAAA | 57097 |
rs751182739 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3819647 | TCCATCACTCTCTTG[C/T]TTAAAGTTCTACAAT | 57097 |
rs751243006 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3831185 | CTTCCATTCCTGGTA[A/C]CTTCTCACTTTTCTT | 57097 |
rs751307986 | snp | C/T | 1.65108e-05 | 0.00287317 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812386 | TGTTCCCATGCTTTA[C/T]GTCATCTTTGCAGAA | 57097 |
rs751363235 | snp | C/T | 3.29614e-05 | 0.00405951 | utr-variant-5-prime, missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3829963 | GACGTGTCCATGTCA[C/T]CCACTTCATTGTTTG | 57097 |
rs751369982 | snp | C/G | | | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3874170 | AAAAATGTAATCAAA[C/G]AATACCTATAGATTT | 57097 |
rs751446577 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3824898 | GAAATACTATTCTCT[A/G]TATTCCACAGAAGTA | 57097 |
rs751481564 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3817365 | ACTAGATTAGATGGT[A/G]CATATATACCAGTTG | 57097 |
rs751575611 | snp | C/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3837264 | TGTCCTAATTATTTA[C/G]TAGAGCTGAGAAAAA | 57097 |
rs751604658 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3861438 | TAATGATGTTGAACA[C/T]CTTTTCATGTTGTTA | 57097 |
rs751637881 | snp | C/G | 1.70991e-05 | 0.00292391 | intron-variant | PARP11 | GRCh38.p7 | 12:3826145 | CTTTCCACCCCTATT[C/G]TCTTTACCATACCTG | 57097 |
rs751679741 | snp | A/C | | | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3875306 | AAAAAATGTCTTGTT[A/C]GTTCTAATAGCTTGA | 57097 |
rs751729442 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3860484 | CAACCCCATCAGAGG[A/G]TCCAGAAGGCAGCAC | 57097 |
rs751844875 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3869144 | TTTAAGGACCCTTGC[A/G]ATTACTTTGGGGCCC | 57097 |
rs751892883 | in-del | -/TGTTA | | | intron-variant | PARP11 | GRCh38.p7 | 12:3835371 | GTTCAGCTATATCAC[-/TGTTA]TGTTATATACACATA | 57097 |
rs751912901 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3820277 | TTGCTGGATGGACTC[A/G]CGTGGGCCTGACTAC | 57097 |
rs751989001 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3828320 | TTGGGAGGTGGAGGC[A/G]GGTGGATCAGGAGGT | 57097 |
rs752033232 | snp | G/T | | | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3870659 | AGTGCCTACTATGTG[G/T]CAGGTTCTGTTCTCT | 57097 |
rs752073998 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3866400 | TTTCTCTCAGAATCT[C/T]CAAAAGACGGTCCTC | 57097 |
rs752123367 | snp | C/T | 1.65072e-05 | 0.00287286 | utr-variant-5-prime, missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3829984 | TCATTGTTTGTTGTT[C/T]TAGAAAATAATTCTT | 57097 |
rs752268638 | in-del | -/AAA | | | intron-variant | PARP11 | GRCh38.p7 | 12:3857967 | GTGTAGAAAGTTTTC[-/AAA]AGTAGTTTAGCATGG | 57097 |
rs752281232 | snp | A/G | 1.6483e-05 | 0.00287076 | intron-variant | PARP11 | GRCh38.p7 | 12:3829885 | AATTAAAGGAAAGGA[A/G]GTACCTGAAACATGT | 57097 |
rs752325215 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3862714 | ACTGTCCTTTTCCCA[C/T]TGAATCGTACCTTTT | 57097 |
rs752334396 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3857048 | AAACCAAACACCGCA[C/T]GTTCTCACTCATAAG | 57097 |
rs752549212 | snp | C/T | 0.000280618 | 0.0118419 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3814066 | GCACCATGTATACCA[C/T]TTATTCTCCAATCAA | 57097 |
rs752573471 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3814809 | ATAGTCATGTATTTA[C/T]ATATAAAAGTTAAAA | 57097 |
rs752587955 | snp | A/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3835913 | TGGGATACCATTAAG[A/T]GCACCAACATATAAA | 57097 |
rs752595189 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3851563 | GGCTTGGGGAGGGGT[G/T]TCCACCATTGCTGAG | 57097 |
rs752642991 | snp | A/T | 1.67758e-05 | 0.00289614 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812421 | CTGGAATAAGCAGCA[A/T]CTCTAGCAAAATAGG | 57097 |
rs752715840 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3850764 | ATTTATATTTATCTA[A/C]AAAACAGAAAGTCAA | 57097 |
rs752761457 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3826976 | CAAAATGATTATGTT[C/T]ACCCACCCAGGCTAA | 57097 |
rs752819399 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3857445 | AAACATCACTGTTTT[G/T]ACATTATTATCCTAG | 57097 |
rs752828070 | snp | A/C/G | 3.43208e-05 | 0.00414239 | intron-variant | PARP11 | GRCh38.p7 | 12:3826268 | ATTAGATAAGTCATA[A/C/G]AAGTACACTGTACTA | 57097 |
rs752870587 | snp | A/G | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3872872 | CGGAGGTTGCGGTGG[A/G]CCGAGATCACGCCAC | 57097 |
rs752882423 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3860213 | AGCAGGACAACTGCC[A/G]ATTTGAAATGAAAAA | 57097 |
rs752884028 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3824774 | TAACATCTTCCATTA[C/T]TATGTCTCATTTTTC | 57097 |
rs752919018 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3828851 | CCTGACCTTCAGAGC[C/T]GTAGATTTTATCATA | 57097 |
rs752960007 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3823396 | AGCATACATTTATTG[C/T]ACCTGTTTTTTTGGT | 57097 |
rs752984092 | snp | C/T | 1.66236e-05 | 0.00288297 | intron-variant | PARP11 | GRCh38.p7 | 12:3821834 | TAACCATAAAAGACA[C/T]AGTGGAAAGGAGAAG | 57097 |
rs753028518 | snp | C/G | 1.69066e-05 | 0.00290741 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3826158 | TTCTCTTTACCATAC[C/G]TGAAAGCACTGATAG | 57097 |
rs753061573 | snp | A/T | | | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3871103 | CTAGTTTCTACTGGA[A/T]AAAAACTTAACTTAA | 57097 |
rs753071853 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3867302 | ACTATTCAGAGTATG[C/T]GCTCTCAGATGTTGC | 57097 |
rs753161165 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3833007 | GTCTGAATCATCAAA[C/T]TGAAAAGCTGTGTGG | 57097 |
rs753178975 | snp | G/T | | | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3873754 | AATATCTCCCTATGA[G/T]TGAGATTATTGAAAG | 57097 |
rs753190921 | in-del | -/GAG | | | intron-variant | PARP11 | GRCh38.p7 | 12:3812581 | TCTGCAGATCTTTAA[-/GAG]GAGAAGAATAGAAAT | 57097 |
rs753216461 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3842535 | GTTGTTGCCGAAGTA[C/T]TTTCTAACAGAAACT | 57097 |
rs753271910 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3817335 | ATAGGCAGGCATGGA[A/C]AACAACGCTTACTTA | 57097 |
rs753279827 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3832212 | GTGGGACAGGTACCA[C/T]TGTATTGAACATTCC | 57097 |
rs753294512 | snp | A/T | 1.78579e-05 | 0.00298808 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812081 | AAACCTTCCTGCAAA[A/T]AAGAATAAAGCTTCC | 57097 |
rs753393076 | in-del | -/G | | | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3873781 | AAAGCATTTAGCACA[-/G]TATTTGGCACACAGA | 57097 |
rs753431361 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3852463 | CTGATGGAGCTGAAA[A/G]CCATGGCACAAGAAC | 57097 |
rs753432485 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3837773 | AGATGTTCCACGCAA[C/T]TGGAAAACAAAGAAG | 57097 |
rs753458327 | in-del | -/G | 1.6654e-05 | 0.00288561 | intron-variant | PARP11 | GRCh38.p7 | 12:3828895 | AACACACAACTATTA[-/G]GGAAAAAAACATACC | 57097 |
rs753475060 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3868886 | TTAAAAACAACACTA[A/C]TTTATTTTCTTACAT | 57097 |
rs753523376 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3854394 | AGACCGCTAGCAAGA[C/T]GAACAAAGAAGAAAA | 57097 |
rs753523435 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3838685 | CATTTTTCAAAAGAT[A/G]AACAAAAATGGACAA | 57097 |
rs753746676 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3863674 | TACAAGGTTCCAAGC[A/G]TCCCTTCCCGGTGCA | 57097 |
rs753791259 | in-del | -/AAGAGA | | | cds-indel, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810716 | AGAGAGAGAGAAGAG[-/AAGAGA]AAGAGAAAGAGAAAG | 57097 |
rs753829567 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3829586 | AGAAGTGTTTAATAC[A/G]GATTTGTTCTTCCCT | 57097 |
rs753838723 | snp | A/C | | | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3871243 | GGGGTTATTAAAGTA[A/C]ATTTATGCAGTTATC | 57097 |
rs753896356 | snp | C/T | 1.83791e-05 | 0.00303137 | intron-variant | PARP11 | GRCh38.p7 | 12:3814234 | CACACAGAAATATAC[C/T]ATAAGTAGCATTTAT | 57097 |
rs754007714 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3831449 | TTTTAGAAGCTGTAG[C/T]AACCTGGAATAAGTT | 57097 |
rs754016983 | snp | C/T | | | intron-variant, utr-variant-5-prime | PARP11, LOC105369609 | GRCh38.p7 | 12:3872500 | AGACACATGAAGTCA[C/T]AATGAAAATACCAGA | 57097 |
rs754070697 | snp | G/T | 1.65083e-05 | 0.00287296 | intron-variant, missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3828924 | CCTGCAAAGTCTATC[G/T]TGTAGCTGAATTTGG | 57097 |
rs754149085 | snp | C/T | 1.64757e-05 | 0.00287012 | synonymous-codon, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3822097 | TACCTGATATGGTAC[C/T]TGAGTATTCACATTC | 57097 |
rs754199023 | in-del | -/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3845440 | CTGTGAACTGCAAAC[-/T]TGCTTATGATTGACT | 57097 |
rs754206396 | snp | C/T | 1.64939e-05 | 0.0028717 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3821990 | TCATGTGTTTGATTG[C/T]GCAGAGGAATAAGCT | 57097 |
rs754252422 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3820076 | GTCCCCTCACTTTGT[A/G]CTCCCATGACTCCCT | 57097 |
rs754300764 | in-del | -/A/AAGAGA | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810715 | AGAGAGAGAGAAGAG[-/A/AAGAGA]AAGAGAAAGAGAAAG | 57097 |
rs754307975 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3845035 | ATTTTTGAGTTGGAA[A/G]TTATGAAACTTCACC | 57097 |
rs754328885 | snp | C/T | | | downstream-variant-500B | PARP11 | GRCh38.p7 | 12:3808634 | TTTTATAATAGCACA[C/T]AGTAAATGATTTTTC | 57097 |
rs754347469 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3809624 | CTGAGAGAGCTATGC[A/G]TATAAAACTTGAAAA | 57097 |
rs754355704 | in-del | -/A | | | intron-variant | PARP11 | GRCh38.p7 | 12:3859561 | AGTGAGACTCTGCTA[-/A]AAAAAAAAAAAAAAA | 57097 |
rs754430679 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3843593 | TTTTCTAGAGGATGC[C/T]GCTAGAAAATGGTTT | 57097 |
rs754513051 | snp | C/T | 1.6476e-05 | 0.00287014 | intron-variant, missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3829002 | TCGATATCTTCACTG[C/T]TAACTGAACACTGAC | 57097 |
rs754565856 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3861661 | TCAACAGCAGAAGTT[C/T]TTAATTTTGATAAAG | 57097 |
rs754666725 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3838808 | GGAAACGAAAGGCCG[A/C]GTCTTTCTTTTTTGG | 57097 |
rs754761526 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810344 | CCTGTAATCTCAGCA[C/T]TTTGGAAGGCTGAGG | 57097 |
rs754815849 | snp | C/T | 1.65132e-05 | 0.00287339 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812388 | TTCCCATGCTTTATG[C/T]CATCTTTGCAGAAAC | 57097 |
rs754871412 | snp | A/G | 1.6476e-05 | 0.00287014 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812256 | TTGGAAGGAGGTCGC[A/G]TGTATTTGGAGTCTC | 57097 |
rs754923500 | snp | G/T | 1.65282e-05 | 0.00287469 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812159 | CTCAGGATAGATTTG[G/T]TTGGCATCAAAAACC | 57097 |
rs754948304 | snp | A/C | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3872531 | GTCAGCCAAGGAAGA[A/C]GGCAGACTTGCAGTT | 57097 |
rs755034458 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3859178 | AAACAAATAAATTCA[G/T]GTTTAGACTTGGGTA | 57097 |
rs755090201 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3823581 | CGCCATGTGGATACA[C/T]CATAATAATATTTAG | 57097 |
rs755115441 | snp | C/T | | | downstream-variant-500B | PARP11 | GRCh38.p7 | 12:3808691 | TCATGATGATTCAAA[C/T]TAAGAACAAGAGACT | 57097 |
rs755149402 | snp | C/T | 1.70394e-05 | 0.0029188 | intron-variant | PARP11 | GRCh38.p7 | 12:3826149 | CCACCCCTATTCTCT[C/T]TACCATACCTGAAAG | 57097 |
rs755150376 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3821164 | ATTTGCAATTTCTCT[A/G]AATAAAAAGTTAAAA | 57097 |
rs755181298 | in-del | -/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3868995 | AATCTATTTCCGTGG[-/T]TTTTCAAGCTTCTAG | 57097 |
rs755188412 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3835741 | GTTGAAAAGTATAGT[A/G]AGTAAAATGAAACAC | 57097 |
rs755214112 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3826695 | CAACTCACAGAATTT[C/T]AAAAATTTCTACATT | 57097 |
rs755366718 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3865648 | CTGAAATCTACCTTA[A/G]CAACAATAAACCACT | 57097 |
rs755400436 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3832193 | CTGTTATAAATCGCT[G/T]TGGGTGGGACAGGTA | 57097 |
rs755417203 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3866408 | AGAATCTTCAAAAGA[C/T]GGTCCTCAGGGATTA | 57097 |
rs755419874 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3809697 | TTGGTATGTAAATTA[A/C]AAATAAATCGAAAAA | 57097 |
rs755518993 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3860123 | GAAAAGAATGAGAAA[A/G]TCTGTTCAGAGGACA | 57097 |
rs755579402 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3866995 | TCCTTGACACATATA[C/T]AGTATATAAGGTAAA | 57097 |
rs755617479 | snp | A/G | 1.64762e-05 | 0.00287016 | synonymous-codon, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812279 | GGAGTCTCCGTTTAT[A/G]TAATCTCCAATTAGC | 57097 |
rs755617940 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3852298 | ACTTTGACGAGTTGA[C/T]AGAAGTTGGCTTCAG | 57097 |
rs755636610 | snp | C/T | 1.71161e-05 | 0.00292536 | splice-acceptor-variant | PARP11 | GRCh38.p7 | 12:3812441 | AGCAAAATAGGTTCC[C/T]TAAACAAAGAGGACC | 57097 |
rs755671862 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3817688 | ATGTCTCAAAATTAT[C/T]CACCTCTTAGGGACT | 57097 |
rs755685808 | snp | C/T | 1.6546e-05 | 0.00287624 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3829995 | TGTTTTAGAAAATAA[C/T]TCTTCTGCTTTGTGA | 57097 |
rs755813805 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3867149 | AAAATTGACAGAGCA[C/T]GAAGTATACAAATAG | 57097 |
rs755816489 | in-del | -/CT | | | intron-variant | PARP11 | GRCh38.p7 | 12:3821719 | CACCTCTTTCACTCC[-/CT]GAGAATGCTGAAGAG | 57097 |
rs755843697 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3828011 | TTCATCAGGTTTTTC[A/G]TGGGATACCCCAAAA | 57097 |
rs755880673 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3847519 | AGGATGGTTCAACAT[A/G]TGCAAATCAATCAAC | 57097 |
rs756036906 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3813035 | ATCTTGAACTCTTGA[A/C]CTCAGGTGATCCACC | 57097 |
rs756042010 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3826806 | ATTCTAGTGATAAGA[A/G]ACTAAGTACTTAAAG | 57097 |
rs756186670 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3820852 | TATAAAGAACACAAG[C/T]TGAAAGCCCCTTATT | 57097 |
rs756197821 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3827011 | AGTATAAAGTGTGTT[A/C]TGTCCTTTCTGTGTT | 57097 |
rs756209928 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3819722 | CTTATAAGGCCCCAC[A/G]TGGTCTAGCCCCCGC | 57097 |
rs756291441 | snp | A/C | | | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3871053 | ATGCACAAGAAGGAA[A/C]CATAATGTGCAACTA | 57097 |
rs756416136 | snp | C/G | 3.33322e-05 | 0.00408228 | synonymous-codon, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3826181 | ACTGATAGAAAAGGG[C/G]GCTCTTTTTATTAAG | 57097 |
rs756494129 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3842264 | AAATGAAAATGAAGT[A/G]TCATATTTTGAGAAG | 57097 |
rs756510557 | snp | C/G | | | utr-variant-5-prime, missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3829978 | TCCACTTCATTGTTT[C/G]TTGTTTTAGAAAATA | 57097 |
rs756543242 | snp | C/T | 1.66217e-05 | 0.0028828 | intron-variant | PARP11 | GRCh38.p7 | 12:3821837 | CCATAAAAGACATAG[C/T]GGAAAGGAGAAGTTT | 57097 |
rs756558847 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3843425 | AGAAATGTTAAAAAT[G/T]TTTAGCTTGACAGGT | 57097 |
rs756669855 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3837859 | AAAAAGAGATAAAGA[A/C]GGTCAATAAATAATG | 57097 |
rs756743105 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3817582 | AAAGTCACAGAACTA[C/T]ACTAAGTTCTTCACA | 57097 |
rs756814035 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3851631 | CTGGGTGGAGCCCAC[C/T]GCAACTCAATGAGGC | 57097 |
rs756849265 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3836034 | ATATATACACACACA[C/T]ATATATATATATACA | 57097 |
rs756873748 | snp | A/G | 1.64857e-05 | 0.00287099 | synonymous-codon, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3814092 | ATCAAAGTTATGAAT[A/G]CAGATTGCTTCCACA | 57097 |
rs756897828 | in-del | -/A | 1.66479e-05 | 0.00288508 | intron-variant | PARP11 | GRCh38.p7 | 12:3828897 | ACACAACTATTAGGG[-/A]AAAAAAACATACCTG | 57097 |
rs756915214 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3864155 | TCAGGAATCGATATT[C/T]GATTTTGTCAAAGGC | 57097 |
rs756927204 | snp | A/G | 1.73156e-05 | 0.00294236 | intron-variant | PARP11 | GRCh38.p7 | 12:3812450 | GGTTCCTTAAACAAA[A/G]AGGACCAAGAAAAGC | 57097 |
rs756982225 | snp | C/T | 1.65647e-05 | 0.00287786 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3830001 | AGAAAATAATTCTTC[C/T]GCTTTGTGAAACATC | 57097 |
rs757029717 | snp | A/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3854454 | AATGATAAAGGGGAT[A/T]TCACCACTGATCCCA | 57097 |
rs757039650 | snp | C/T | 1.7303e-05 | 0.00294129 | intron-variant | PARP11 | GRCh38.p7 | 12:3826282 | AAAAGTACACTGTAC[C/T]ATAAAGTGTCATGAA | 57097 |
rs757070994 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3860489 | CCATCAGAGGGTCCA[A/G]AAGGCAGCACTTCCA | 57097 |
rs757209981 | in-del | -/AAG | | | intron-variant | PARP11 | GRCh38.p7 | 12:3860390 | TCCTTGGTTCAACAA[-/AAG]AAGGGACCACTGCCT | 57097 |
rs757293579 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3833120 | AATTTTAGTTTACTA[A/C]AACAAAGTATAATTT | 57097 |
rs757447309 | snp | A/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3867420 | ATGAGGGATGAGATT[A/T]TAAAAAACAAAAAAA | 57097 |
rs757522935 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3845619 | CAAGGTCCACTCTAG[C/T]GTAGCTGAAGAGAAT | 57097 |
rs757534017 | in-del | -/A | | | intron-variant | PARP11 | GRCh38.p7 | 12:3833717 | AAACATTCATTCAAG[-/A]AAAATGTACTCAATC | 57097 |
rs757622536 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3820331 | GTGACAGTGAGACAG[A/G]CAAAGTTATTTTAGT | 57097 |
rs757673726 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3820168 | CCATTATATCCCAAG[G/T]GCCCAGAACAGTGCT | 57097 |
rs757717146 | snp | C/G | 1.64947e-05 | 0.00287177 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3821994 | GTGTTTGATTGTGCA[C/G]AGGAATAAGCTGGAA | 57097 |
rs757756712 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3853331 | CCCAATTAAAAGACA[C/T]AGACTGGCAAATTGG | 57097 |
rs757774355 | snp | A/C | 1.65362e-05 | 0.00287538 | stop-gained, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3821886 | ACCTGCAAAAGAACT[A/C]CCACAAATCTAGGTT | 57097 |
rs757893127 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3869464 | ATGGCCTGGTTCCTA[C/T]CTCCTGGGCTTGTCT | 57097 |
rs757953603 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3864114 | GAGCAAGTTCCTTTC[C/T]ATTCCTAGGCTGCTG | 57097 |
rs758007668 | snp | C/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3849491 | AAAGAATGGAGTCAT[C/G]ACATTGGCAGCAACA | 57097 |
rs758011826 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3817280 | AGTTTCTCTTAGATA[C/T]TATAAATAAACTGTG | 57097 |
rs758073531 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3857195 | GACGAGTTAATGGGG[A/G]CAGCAAACCAACATG | 57097 |
rs758085312 | snp | A/C/G | 3.32609e-05 | 0.00407793 | intron-variant | PARP11 | GRCh38.p7 | 12:3821822 | ATATTTATGTTTTAA[A/C/G]CATAAAAGACATAGT | 57097 |
rs758133792 | snp | C/T | | | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3871405 | GTTTAGATACATAAA[C/T]ACTTTCCATTGTGTT | 57097 |
rs758141149 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3823398 | CATACATTTATTGCA[C/T]CTGTTTTTTTGGTTT | 57097 |
rs758169815 | snp | A/T | 5.01324e-05 | 0.00500637 | stop-gained, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812139 | CAATGAAAGTCTATC[A/T]AGTACTCAGGATAGA | 57097 |
rs758223932 | snp | C/T | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3872969 | GGGATGAGGCTGAAA[C/T]ATCACGGGAAGTAAA | 57097 |
rs758257341 | in-del | -/AT | 3.29587e-05 | 0.00405934 | frameshift-variant, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3829897 | GGAGGTACCTGAAAC[-/AT]GTGCCACTTCCCACA | 57097 |
rs758261385 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3835914 | GGGATACCATTAAGT[A/G]CACCAACATATAAAT | 57097 |
rs758281564 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3837002 | CAGGAAGCACTGGGA[A/G]TACCTGAAGGGAGAA | 57097 |
rs758287056 | snp | C/T | 4.94336e-05 | 0.00497135 | intron-variant, missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3828969 | ATGGAGCCACAAGGG[C/T]TTGTTTTGAAGCTTT | 57097 |
rs758316116 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3842149 | GTCTGAAAGAAAAAA[C/T]AGAAAAAGTAAAAGA | 57097 |
rs758338547 | snp | C/T | 1.67888e-05 | 0.00289726 | intron-variant | PARP11 | GRCh38.p7 | 12:3828867 | GTAGATTTTATCATA[C/T]CAATATACTAAAAAC | 57097 |
rs758418251 | snp | C/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3834265 | AGCCATAAGGACAAA[C/G]AGCTCTACATTTCCA | 57097 |
rs758442358 | snp | C/T | | | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3874457 | AGAGACAGGTTTTCG[C/T]CATGTTGGCCAGGCC | 57097 |
rs758449865 | in-del | -/AA | 1.72898e-05 | 0.00294017 | intron-variant | PARP11 | GRCh38.p7 | 12:3812447 | ATAGGTTCCTTAAAC[-/AA]AGAGGACCAAGAAAA | 57097 |
rs758501749 | snp | C/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3844017 | TTTGACAAACTGAAA[C/G]AGATGAGTTTTCTGG | 57097 |
rs758606394 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3824851 | ATTATATTATTTGTA[A/C]TAAAGAATGTGGATA | 57097 |
rs758812806 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3817985 | GATCTAAATTCACAT[C/T]ATTAACAAGATGCTC | 57097 |
rs758829410 | in-del | -/CT | | | intron-variant | PARP11 | GRCh38.p7 | 12:3819741 | TCTAGCCCCCGCTAA[-/CT]CTCTGACTTCCACTC | 57097 |
rs758839073 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3819196 | CTTATTCACTCCATC[A/G]CATACAATAAGTGAG | 57097 |
rs758844430 | snp | C/T | 3.295e-05 | 0.00405881 | synonymous-codon, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3822124 | ATTCTCCCAGTGTGG[C/T]GGCATAGGGATGGCC | 57097 |
rs758986836 | snp | C/T | 1.70606e-05 | 0.00292062 | intron-variant | PARP11 | GRCh38.p7 | 12:3822208 | GCCGATTACAATTAC[C/T]GTCAAGAACTTAGCC | 57097 |
rs759076199 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3856838 | GCACACATACGTTTA[C/T]TGTGGCACTATTCAC | 57097 |
rs759160235 | snp | C/T | 1.64754e-05 | 0.00287009 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3822089 | TCTGCTCTTACCTGA[C/T]ATGGTACTTGAGTAT | 57097 |
rs759201157 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3824785 | ATTATTATGTCTCAT[G/T]TTTCATTTTTCTCCC | 57097 |
rs759277155 | snp | C/T | | | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3870575 | AGGGAAAATTCATAG[C/T]AGGAGCAAAGAATTA | 57097 |
rs759304554 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3830597 | AAAAAAGTCTGGATG[G/T]ATATATAACAATCTA | 57097 |
rs759310927 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3862362 | GGAGACAGGCAAGAG[A/G]ATTGCTTGAGCCCAG | 57097 |
rs759328929 | snp | C/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3864294 | ACATCAGTAGGTCAT[C/G]ATGTATTAATCCTTT | 57097 |
rs759351150 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3829642 | TGGAGTTGCTCAGAT[A/G]TACTGACACCATGCA | 57097 |
rs759354996 | snp | G/T | 1.64928e-05 | 0.00287161 | utr-variant-5-prime, missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3829973 | TGTCATCCACTTCAT[G/T]GTTTGTTGTTTTAGA | 57097 |
rs759427457 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3842945 | ATTCCAAACATAACG[C/T]TGCACCAAATAGAAA | 57097 |
rs759533232 | snp | A/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3814609 | ATCCTCAGAAACTAG[A/T]AAATGTTGGTTCAGT | 57097 |
rs759660522 | in-del | -/TTC | | | intron-variant | PARP11 | GRCh38.p7 | 12:3831112 | ACTACATAAAAAATA[-/TTC]TTCTTGCAAAAAATC | 57097 |
rs759672992 | snp | C/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3852025 | CAGCAAACTCCAACA[C/G]ACGTGCAGCAGAGGA | 57097 |
rs759678942 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3824707 | GTGTTTGATCCCATC[A/G]CAGTGTTTCTTGTCT | 57097 |
rs759685861 | snp | A/G | | | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3873906 | GTTTAGAAAAGTTAA[A/G]AAGTGCAATATGATT | 57097 |
rs759695271 | snp | C/T | 1.67455e-05 | 0.00289352 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3814181 | TTTTCTTGAGCTGAG[C/T]CTTTTTCCTAAAAAC | 57097 |
rs759812726 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3856382 | CCATCTGACAAAGGG[C/T]GAATATCCAGAATCT | 57097 |
rs759839723 | snp | C/T | 1.79078e-05 | 0.00299226 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812073 | TGAAGAGCAAACCTT[C/T]CTGCAAAAAAGAATA | 57097 |
rs759841748 | in-del | -/ACAATA | | | intron-variant | PARP11 | GRCh38.p7 | 12:3830639 | TCTAAGTGTCAGGAT[-/ACAATA]ACAATAATAGTAACC | 57097 |
rs759864572 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810653 | GGAGGGAAAGAAGGA[A/G]GGAAGGAAGGAAGGA | 57097 |
rs759987332 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3825752 | TTTTTGAGATGGAGT[C/T]TCACTCTGTCGCCCA | 57097 |
rs760004987 | snp | A/G | | | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3874650 | GAAATAATCTACTGA[A/G]TAGACGTTTGAGTGG | 57097 |
rs760051771 | snp | A/C | 1.66955e-05 | 0.0028892 | intron-variant | PARP11 | GRCh38.p7 | 12:3828889 | ACTAAAAACACACAA[A/C]TATTAGGGAAAAAAA | 57097 |
rs760166878 | in-del | -/T | 1.7306e-05 | 0.00294155 | intron-variant | PARP11 | GRCh38.p7 | 12:3826130 | AAAAAAAACCCACTC[-/T]TTTCCACCCCTATTC | 57097 |
rs760191744 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3854373 | GAAAAGATCAACAAA[A/G]TTGATAGACCGCTAG | 57097 |
rs760193858 | snp | C/T | | | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3870476 | ATAACAAATCAAGTA[C/T]ATAAGACATTCATTA | 57097 |
rs760198578 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3825514 | GGCTCTGAGAGAGTA[C/T]GTCCAAGTTAACAAT | 57097 |
rs760231826 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3833509 | CTTGAGAGGCTGAGA[C/T]GGAAGGATTACTTGA | 57097 |
rs760257043 | snp | C/T | 3.38484e-05 | 0.00411376 | intron-variant | PARP11 | GRCh38.p7 | 12:3826241 | CTTCATTTCTGTATA[C/T]AAAGACAAGATATTA | 57097 |
rs760336456 | in-del | -/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3825714 | ATGAGAGATTTGATA[-/T]TTTTTTAATTAATTA | 57097 |
rs760354444 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3832924 | GGCAATGGGTATGCT[A/G]GTAGAGCCTGTCCGT | 57097 |
rs760459094 | snp | C/T | 1.64871e-05 | 0.00287111 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3814087 | CTCCAATCAAAGTTA[C/T]GAATGCAGATTGCTT | 57097 |
rs760537896 | snp | C/T | 1.74842e-05 | 0.00295665 | intron-variant | PARP11 | GRCh38.p7 | 12:3814221 | ACAGACACAAAAGCA[C/T]ACAGAAATATACCAT | 57097 |
rs760545425 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3816444 | TTGTCTACTAGTTTT[C/T]CTCTTTGAAATACCC | 57097 |
rs760569768 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3856744 | AAGGATCTAGAACTA[G/T]AAATACTATTTGACC | 57097 |
rs760586990 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3829513 | CATCTGCTTCCAAGT[C/T]ACTGTGAGGATAAGG | 57097 |
rs760735420 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3818852 | TATTGGTTTTCTCCC[A/G]CTTTCTGTGGTTGTC | 57097 |
rs760832367 | snp | A/T | 5.34326e-05 | 0.00516851 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812090 | TGCAAAAAAGAATAA[A/T]GCTTCCTTGACCACC | 57097 |
rs760832492 | snp | C/G | 1.64933e-05 | 0.00287165 | intron-variant | PARP11 | GRCh38.p7 | 12:3829046 | CTTTAAGACAAACCA[C/G]AAAGTTTCATTTACC | 57097 |
rs760838526 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3856472 | AAAGGATATGAATAG[A/C]CACTTTTCAAAAGGA | 57097 |
rs760846552 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3863633 | AAGGGGAAACGCACA[C/T]GGGGTGAAGTCTAGA | 57097 |
rs760915174 | in-del | -/A | | | intron-variant | PARP11 | GRCh38.p7 | 12:3846757 | GCGAGACTCCGTCTT[-/A]AAAAAAAAAAAAAAG | 57097 |
rs760920385 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3814519 | CTAAAAATGAGACAA[C/T]AAACAAGTAATACAA | 57097 |
rs760926267 | in-del | -/A | | | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3840354 | ACCTTCCACTTCTGG[-/A]CAAAATTTCCATTCT | 57097 |
rs760944276 | snp | G/T | | | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3873614 | GCTGGCTGTATTTCT[G/T]TCCTATGAAACAAAT | 57097 |
rs760976644 | snp | A/G | | | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3873987 | GTAGAGTGTCAGGAA[A/G]GCTCCCTCAAGATGT | 57097 |
rs761010481 | in-del | -/TC | | | intron-variant | PARP11 | GRCh38.p7 | 12:3831247 | CATATCTTTCAGATC[-/TC]TCTCTCTCTCTCTCA | 57097 |
rs761078484 | in-del | -/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3852597 | AAAAAAGAGTAAAAA[-/G]AAATGAACAAAGCCT | 57097 |
rs761087123 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3825609 | GCAAACTGTTCTAAA[G/T]AATTAAAAAATGTAA | 57097 |
rs761125614 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3822967 | CAGTCCACTACCTTT[A/G]AGGGTTATTAGCACA | 57097 |
rs761201225 | snp | C/T | 3.29544e-05 | 0.00405908 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812217 | TCCACACAGCTGTCA[C/T]ATAAATTCACATAGC | 57097 |
rs761298747 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3832854 | GTAATTAGAAGCAGG[A/C]TGGGAAGAAGAAAAA | 57097 |
rs761367783 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3832124 | CTTACCTAAGACTTC[A/G]CTTTAGGCCAGGTTA | 57097 |
rs761397585 | snp | A/G | 1.82827e-05 | 0.00302341 | intron-variant | PARP11 | GRCh38.p7 | 12:3814235 | ACACAGAAATATACC[A/G]TAAGTAGCATTTATT | 57097 |
rs761427596 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3841911 | AGTAGATGAGTTTCC[A/G]GCAGCCAGGAGTGAA | 57097 |
rs761449373 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3817384 | ATATACCAGTTGAAG[A/G]CAGAGGGCAGGGGCA | 57097 |
rs761459663 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810524 | GAACCCGGGAGGTGG[A/T]GGTTGCAGTGAGCCG | 57097 |
rs761480621 | in-del | -/A | | | intron-variant | PARP11 | GRCh38.p7 | 12:3817003 | CAGACCATCCTAGCT[-/A]ACATGGTGAAACCCT | 57097 |
rs761520034 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3844834 | CATGAAGGTTGGTTT[C/T]GCTTTTATCCTTTAA | 57097 |
rs761595065 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3818775 | TTTCAGTATGTAATC[A/G]TACAGATGGCACCTA | 57097 |
rs761637207 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3844143 | AATTACCTAACGTCC[A/G]TGTAACTGCTGATTT | 57097 |
rs761695124 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3852242 | TCCTCCAAAGGAACG[A/C]AGCTCCTTGCAAGCA | 57097 |
rs761764581 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3812852 | CTGTCTCCCAAGCTG[A/G]AGTGCAGTGGCGCGA | 57097 |
rs761774665 | in-del | -/CTTT | | | intron-variant | PARP11 | GRCh38.p7 | 12:3869538 | TCAAGCACCAAGCTC[-/CTTT]CTTTCTCAGGATCTT | 57097 |
rs761778024 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3868679 | CATCTAAGATGCAGC[C/T]TGAATTGATCTCCTC | 57097 |
rs761779630 | snp | C/T | 1.64966e-05 | 0.00287194 | synonymous-codon, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3821941 | TCGGTTGCGATCCAT[C/T]GTCTTCCCAAAGAGA | 57097 |
rs761787348 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3859324 | AATCCTAGCACTTTG[C/T]GAGGCCGAGGCGAGT | 57097 |
rs761850580 | snp | C/G | 4.94319e-05 | 0.00497127 | synonymous-codon, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812225 | GCTGTCATATAAATT[C/G]ACATAGCTCCCGTCT | 57097 |
rs761895348 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3841729 | TTAGGCCCAGTTCCT[A/G]TTGCACCTCCTTTCT | 57097 |
rs761903517 | snp | A/T | 1.65067e-05 | 0.00287282 | intron-variant | PARP11 | GRCh38.p7 | 12:3829067 | TTCATTTACCAGCTG[A/T]TCACATTAATGACTT | 57097 |
rs761950257 | snp | C/T | 1.64784e-05 | 0.00287035 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812337 | GTTCTAAACAGATGC[C/T]GCTGTTGCAAGCTGA | 57097 |
rs761958337 | snp | A/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3861469 | TTTTCCATCTGCTTA[A/T]CTTCTTTGGTGCAGT | 57097 |
rs762058928 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3835389 | TTATATACACATAAA[C/T]CAATAACCAAACAAA | 57097 |
rs762082045 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3827840 | ACTAACACTGTCATA[A/G]AGACACTACTCACAG | 57097 |
rs762146923 | snp | C/T | | | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3821927 | TGAATTCTTTTAATT[C/T]GGTTGCGATCCATCG | 57097 |
rs762158620 | snp | A/G | 1.73954e-05 | 0.00294913 | intron-variant | PARP11 | GRCh38.p7 | 12:3826119 | CAATAGTAAGAAAAA[A/G]AAAACCCACTCTTTC | 57097 |
rs762198526 | snp | A/G | | | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3870788 | TTGGGTGGCTAAAGG[A/G]TTTGTTATGGAAAAA | 57097 |
rs762209914 | snp | C/T | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3822102 | GATATGGTACTTGAG[C/T]ATTCACATTCTCCCA | 57097 |
rs762339761 | snp | C/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3834029 | GGTAGAATTTCTATT[C/G]CAGGTACAGCAGGCT | 57097 |
rs762355571 | snp | A/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3859837 | GACTTCAAACCAAAA[A/T]GTGTTACTATAAAAA | 57097 |
rs762367518 | snp | A/C | 1.64792e-05 | 0.00287042 | intron-variant | PARP11 | GRCh38.p7 | 12:3822067 | TTCATGGGTATATTC[A/C]GTCAATTCTGCTCTT | 57097 |
rs762371603 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3844504 | AGATTTGAAAGTTCA[A/G]TGTGTTTGATCTCAG | 57097 |
rs762451064 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3830817 | CAACAAGGAAGTCAA[G/T]ATTCAAACCCAACAT | 57097 |
rs762506843 | in-del | -/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3812705 | ACCAAAATATAGCTA[-/T]CAGACTTCTGTTTTT | 57097 |
rs762526940 | in-del | -/AA | | | intron-variant | PARP11 | GRCh38.p7 | 12:3866124 | AACAAACAAACAAAC[-/AA]AAGACACTTCCTAGG | 57097 |
rs762575037 | snp | C/G | 1.64963e-05 | 0.00287192 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3821955 | TCGTCTTCCCAAAGA[C/G]ATTAGCAACTTCATT | 57097 |
rs762584129 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3845029 | ATTTGCATTTTTGAG[G/T]TGGAAATTATGAAAC | 57097 |
rs762612095 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3823999 | CTGTAAAATAACATA[C/T]TTGAAACAGAATTTC | 57097 |
rs762637611 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3819472 | GCTTCTATCCAGTAG[A/G]TGCCAGGAGCACCCC | 57097 |
rs762639666 | snp | G/T | | | downstream-variant-500B | PARP11 | GRCh38.p7 | 12:3808443 | AATGTTTAACTCAGT[G/T]CAACAGGAATGATGG | 57097 |
rs762709388 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3817247 | ATTCGATTGAATCTC[A/G]GTTTGAAAATTCACT | 57097 |
rs762727764 | snp | C/T | 1.64773e-05 | 0.00287026 | utr-variant-5-prime, missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3829956 | GGTATCTGACGTGTC[C/T]ATGTCATCCACTTCA | 57097 |
rs762776964 | snp | A/G | 4.95364e-05 | 0.00497652 | intron-variant | PARP11 | GRCh38.p7 | 12:3829849 | AAGGTGATGCTAAGT[A/G]AATCGAAAACACTTC | 57097 |
rs762789419 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3818625 | CCTCCTCACTGCCAA[A/G]CTTCTTGAAAAAGTT | 57097 |
rs762801782 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3866565 | ATTCACTATAATATC[C/T]CATTATATTCACTCT | 57097 |
rs762824019 | snp | A/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3832099 | ACATGTGTGCTCCGC[A/T]ATAAAACACCTTACC | 57097 |
rs762834541 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3851564 | GCTTGGGGAGGGGTT[C/T]CCACCATTGCTGAGG | 57097 |
rs762836943 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3822689 | AAAATATCCAACCCT[A/G]TATATCATAAAAATT | 57097 |
rs762843684 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3865373 | TGCCAAGCAGATCAA[G/T]TTAGTTGACAGTGGT | 57097 |
rs762917543 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3826018 | ACAGGTGTGAGCCAC[C/T]GCGCCTGGCCCAAGA | 57097 |
rs763019890 | snp | C/T | 1.64972e-05 | 0.00287199 | synonymous-codon, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812375 | AATTTGGAATGTGTT[C/T]CCATGCTTTATGTCA | 57097 |
rs763045068 | snp | C/G | 1.68929e-05 | 0.00290623 | intron-variant | PARP11 | GRCh38.p7 | 12:3814018 | GGGCTCAAATTGGAC[C/G]TGGAATTCTGATAAT | 57097 |
rs763145389 | in-del | -/AACA | | | intron-variant | PARP11 | GRCh38.p7 | 12:3847361 | ACCCAATAAGGACAC[-/AACA]AACAAAGAAAACCAT | 57097 |
rs763148637 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PARP11 | GRCh38.p7 | 12:3811731 | CTCTAAAGGGACACA[C/T]TTATGTCTGTATTTT | 57097 |
rs763214104 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3848606 | AAAGACTATCTAATT[C/T]GCAGAAGAATAAAAC | 57097 |
rs763227012 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3837882 | AAATAATGATAATGG[A/G]GTCAACGAAGCAAGT | 57097 |
rs763230070 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3833822 | TGAAGCCTCTACCTG[C/T]GGTATATGTACCCAA | 57097 |
rs763269296 | in-del | -/T | 3.295e-05 | 0.00405881 | frameshift-variant, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3822097 | TACCTGATATGGTAC[-/T]TGAGTATTCACATTC | 57097 |
rs763281097 | snp | A/G | 1.70098e-05 | 0.00291627 | intron-variant | PARP11 | GRCh38.p7 | 12:3826253 | ATACAAAGACAAGAT[A/G]TTAGATAAGTCATAA | 57097 |
rs763292043 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3850979 | TCTTGTTCATGTATT[G/T]AAAGGATAGTCCATC | 57097 |
rs763451965 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3830861 | TCTACGCACTTAGCC[A/G]CCGTCATATACTGTC | 57097 |
rs763604589 | in-del | -/AC | 3.45784e-05 | 0.00415789 | intron-variant | PARP11 | GRCh38.p7 | 12:3826280 | ATAAAAGTACACTGT[-/AC]TATAAAGTGTCATGA | 57097 |
rs763627884 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3816185 | CTTTATAAAAACAAA[C/T]GAAAAAAGTTTTTTA | 57097 |
rs763640495 | snp | A/G/T | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3811044 | ACAGCAAAACAGATG[A/G/T]AACAGGTAAACAAAT | 57097 |
rs763776367 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3842118 | GTTGAACTTGAACCT[A/G]AAAGGACCATTCAAA | 57097 |
rs763816578 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3858969 | AGGTGTGGTGGTAGG[C/T]GCCTGTAATCCCAGT | 57097 |
rs763913162 | snp | C/T | 7.25084e-05 | 0.00602071 | intron-variant | PARP11 | GRCh38.p7 | 12:3814233 | GCACACAGAAATATA[C/T]CATAAGTAGCATTTA | 57097 |
rs763941815 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3866595 | TCTGTTGATACATTC[A/G]TATCAGCCATAGTTA | 57097 |
rs764001725 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3816708 | GATCTGCAATGACTA[G/T]AATCCACTCTAAGGA | 57097 |
rs764071418 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3817349 | AAAACAACGCTTACT[C/T]ACTAGATTAGATGGT | 57097 |
rs764076062 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3865378 | AGCAGATCAAGTTAG[C/T]TGACAGTGGTGTTCA | 57097 |
rs764107623 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3812664 | GTACAGACCAGTCCT[C/T]ACCACCAACACCATC | 57097 |
rs764119678 | snp | A/C/T | 0.000115401 | 0.00759529 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3814091 | AATCAAAGTTATGAA[A/C/T]GCAGATTGCTTCCAC | 57097 |
rs764170775 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3811014 | TCCAACACTTCTCAT[A/C]TTCCTTACAATGAAA | 57097 |
rs764244947 | snp | A/C | 1.72573e-05 | 0.00293741 | intron-variant | PARP11 | GRCh38.p7 | 12:3826276 | AGTCATAAAAGTACA[A/C]TGTACTATAAAGTGT | 57097 |
rs764310769 | snp | C/T | | | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3875284 | CCTTGTATCCTACCA[C/T]ACTATGAAAAAATGT | 57097 |
rs764310865 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3860478 | TGTGACCAACCCCAT[C/T]AGAGGGTCCAGAAGG | 57097 |
rs764323931 | snp | A/C | 0.00010597 | 0.0072783 | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812100 | AATAAAGCTTCCTTG[A/C]CCACCGAGATTTGGA | 57097 |
rs764342473 | snp | C/T | 1.65669e-05 | 0.00287805 | intron-variant | PARP11 | GRCh38.p7 | 12:3828907 | TTAGGGAAAAAAACA[C/T]ACCTGCAAAGTCTAT | 57097 |
rs764376884 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3837910 | AGTGGACATAATTAT[A/G]AATATCTATGCACTC | 57097 |
rs764460975 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3833856 | ACAGGCAGAGGGCTC[C/T]CTCTCCCTCAGGCTT | 57097 |
rs764461554 | in-del | -/TC | | | intron-variant | PARP11 | GRCh38.p7 | 12:3832462 | TACCAAGCCCCACTG[-/TC]TCTCCTTTTCACACA | 57097 |
rs764475687 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3809317 | TAACTCTGTACTATC[A/G]TATTTTAAAATATGT | 57097 |
rs764483434 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3868967 | TGATTCCCTTCTAAA[G/T]GTTGTATGAGAGAAT | 57097 |
rs764705301 | in-del | -/A | | | intron-variant | PARP11 | GRCh38.p7 | 12:3838043 | GGGACTTCCAGCCAG[-/A]AAATCAACAACAACA | 57097 |
rs764728115 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3848607 | AAGACTATCTAATTC[A/G]CAGAAGAATAAAACT | 57097 |
rs764769868 | in-del | -/T | 4.94303e-05 | 0.00497119 | intron-variant, frameshift-variant, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3828969 | ATGGAGCCACAAGGG[-/T]TTGTTTTGAAGCTTT | 57097 |
rs764779903 | snp | C/T | | | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3870648 | AATATTTATTGAGTG[C/T]CTACTATGTGTCAGG | 57097 |
rs764785877 | snp | A/G | 1.85379e-05 | 0.00304444 | intron-variant | PARP11 | GRCh38.p7 | 12:3814239 | AGAAATATACCATAA[A/G]TAGCATTTATTAATC | 57097 |
rs764880317 | snp | G/T | 6.59228e-05 | 0.00574083 | intron-variant, synonymous-codon, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3828956 | AGTAGTAAAAGAAAT[G/T]GAGCCACAAGGGTTT | 57097 |
rs764898715 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3819203 | ACTCCATCGCATACA[A/G]TAAGTGAGGCGCCAA | 57097 |
rs764989418 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3817059 | AGCCAGGCGTGGTGG[C/T]GGGCGCCTGTAGTCC | 57097 |
rs765028699 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3821775 | CAAGAGAAAAACAGC[A/G]TGTCTACACCACTGA | 57097 |
rs765127705 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3829669 | TGCAACTCTCAGTCA[C/T]ATTCACCCTCTATTG | 57097 |
rs765170964 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3837847 | AACAAGTCCTGTAAA[A/G]AGAGATAAAGAAGGT | 57097 |
rs765262941 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3825808 | CTCGGCTCACTTCAA[A/G]CTCCGCCTCACGGGT | 57097 |
rs765264204 | snp | A/T | | | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3873919 | AAAAAGTGCAATATG[A/T]TTTATAGGTAATATG | 57097 |
rs765277806 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3814747 | ACTGATTGTAACAGA[A/C]AACAAAAACTGAAAA | 57097 |
rs765339646 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3833596 | CACGGCAGAACCCTG[C/T]CTCACAAAAATTAAT | 57097 |
rs765348682 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3835813 | CAGCAAACTTGAACA[C/T]AAATTAATAGACATT | 57097 |
rs765469745 | snp | C/G | 1.6477e-05 | 0.00287024 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812231 | ATATAAATTCACATA[C/G]CTCCCGTCTTTGGAA | 57097 |
rs765520793 | snp | C/T | 3.30447e-05 | 0.00406464 | intron-variant | PARP11 | GRCh38.p7 | 12:3829843 | ATCAGCAAGGTGATG[C/T]TAAGTGAATCGAAAA | 57097 |
rs765540843 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3848092 | ATATAAAATACATAC[A/G]AGTCAATTTAACTAA | 57097 |
rs765592829 | snp | C/T | | | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3821982 | CATTATATTCATGTG[C/T]TTGATTGTGCAGAGG | 57097 |
rs765641605 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3832194 | TGTTATAAATCGCTT[C/T]GGGTGGGACAGGTAC | 57097 |
rs765644533 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3860200 | TGTGGACCGCCCCAG[A/C]AGGACAACTGCCAAT | 57097 |
rs765698455 | snp | G/T | 1.64746e-05 | 0.00287002 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3822105 | ATGGTACTTGAGTAT[G/T]CACATTCTCCCAGTG | 57097 |
rs765729308 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3832937 | CTGGTAGAGCCTGTC[C/T]GTAATGTTATCTGTT | 57097 |
rs765732314 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3845360 | TGCCGATATATCTTA[C/T]TTAATGCAGACTGTA | 57097 |
rs765782221 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810776 | AAAGAGGAAGAGGAG[A/C]GGAAGAGAAGAGGAA | 57097 |
rs765917945 | snp | C/G | 1.64958e-05 | 0.00287187 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3821964 | CAAAGAGATTAGCAA[C/G]TTCATTATATTCATG | 57097 |
rs765921112 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3820063 | CAAAGGTGGATGGGT[C/T]CCCTCACTTTGTGCT | 57097 |
rs766005186 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3867201 | TACTAAAAGATTCTT[G/T]ATATGAAACAGGAGT | 57097 |
rs766035091 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3816550 | GACTGTCTAAGGGGC[C/T]TATCCATCTACCACT | 57097 |
rs766049194 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3862470 | AAATAAATATATGTA[G/T]TTTTTTTTCTATTTT | 57097 |
rs766070981 | in-del | -/CAC | | | intron-variant | PARP11 | GRCh38.p7 | 12:3845046 | GAAATTATGAAACTT[-/CAC]CACCATATTATGATC | 57097 |
rs766107782 | snp | C/T | 1.64781e-05 | 0.00287033 | utr-variant-5-prime, missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3829958 | TATCTGACGTGTCCA[C/T]GTCATCCACTTCATT | 57097 |
rs766182881 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3819034 | TTTGTCTCTAGTCTA[C/T]ACCACTCTTCTCAAC | 57097 |
rs766382568 | in-del | -/AG | | | intron-variant | PARP11 | GRCh38.p7 | 12:3814607 | TTATCCTCAGAAACT[-/AG]AAAATGTTGGTTCAG | 57097 |
rs766389449 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3836719 | CAGCACCAAGATTAT[A/C]GCCAGCAATATCCCA | 57097 |
rs766399834 | snp | A/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3828037 | CAAAACATGCCCATA[A/T]AACACAGATGAAATC | 57097 |
rs766444832 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PARP11 | GRCh38.p7 | 12:3811836 | GATCTCAATGACCAC[A/G]TTAGTTGAGACTCAG | 57097 |
rs766489349 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3849197 | AGAAAATGGAACCCT[C/T]GTTCACTGTTGGTGG | 57097 |
rs766524133 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3851047 | GATCATGAAATAATC[A/G]AAGATCATGATGAAC | 57097 |
rs766663631 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3815687 | CAGCAAACTGCATCC[A/G]TAATCAAGTGTGTAG | 57097 |
rs766679937 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3823328 | GGTATTCTTCCAGAG[C/T]TTCTTTAGGTTAATA | 57097 |
rs766690366 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3850535 | CCAGATTCCCCCACG[C/T]AAGCATGTCCACAAA | 57097 |
rs766726753 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3852668 | TTGATTGGTGTACCT[A/G]AAAGTGACGGGGCGA | 57097 |
rs766759756 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3809606 | AGTTTTTCCATTCAA[C/G]TGCTGAGAGAGCTAT | 57097 |
rs766783554 | snp | A/G | | | intron-variant, utr-variant-5-prime | PARP11, LOC105369609 | GRCh38.p7 | 12:3872408 | ATCCTTACAATGGGT[A/G]GTGAGGAAAGGTACT | 57097 |
rs766821647 | snp | C/T | 6.92203e-05 | 0.00588263 | intron-variant | PARP11 | GRCh38.p7 | 12:3826130 | AAAAAAAAACCCACT[C/T]TTTCCACCCCTATTC | 57097 |
rs766836651 | in-del | -/AAACA | | | intron-variant | PARP11 | GRCh38.p7 | 12:3866120 | TAAAAACAAACAAAC[-/AAACA]AAAGACACTTCCTAG | 57097 |
rs766841683 | snp | A/G | | | downstream-variant-500B | PARP11 | GRCh38.p7 | 12:3808628 | ATTTTTTTTTATAAT[A/G]GCACACAGTAAATGA | 57097 |
rs766856869 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3828205 | TTGTTCTTGAAACTA[C/T]TGCCAGCTACCTATG | 57097 |
rs766868446 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3817480 | GGCAGCCACGAAATG[C/T]GGACATTCACAGACT | 57097 |
rs766878348 | snp | A/T | 1.7072e-05 | 0.00292159 | intron-variant | PARP11 | GRCh38.p7 | 12:3826259 | AGACAAGATATTAGA[A/T]AAGTCATAAAAGTAC | 57097 |
rs766899345 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3822964 | CAACAGTCCACTACC[C/T]TTAAGGGTTATTAGC | 57097 |
rs766914958 | snp | C/T | | | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3873642 | AATTTTTATTGATCA[C/T]CGTGTAACGACCAAG | 57097 |
rs766917790 | in-del | -/A | 0.0122028 | 0.0771523 | intron-variant | PARP11 | GRCh38.p7 | 12:3826114 | CTGTCCAATAGTAAG[-/A]AAAAAAAAACCCACT | 57097 |
rs766988666 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3832882 | AAAGCTAGTACAAAG[C/T]GGCAAAGCATTTTGT | 57097 |
rs766998446 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3859157 | TGTGTGTAAAAGGCA[C/T]ATATGAAACAAATAA | 57097 |
rs767074497 | snp | C/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3818981 | TTCTTCATTCCTATA[C/G]TTTCTATTACCCCAC | 57097 |
rs767161017 | snp | C/T | | | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3840213 | ATTTTTGAATGCAGA[C/T]GTTCAAGGAGTTCAT | 57097 |
rs767169230 | snp | A/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3865506 | CTTATTGCTATTCTA[A/T]TAATTTTGTTTCATG | 57097 |
rs767187900 | snp | C/T | 3.29506e-05 | 0.00405884 | synonymous-codon, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3822091 | TGCTCTTACCTGATA[C/T]GGTACTTGAGTATTC | 57097 |
rs767357669 | snp | C/T | 1.65411e-05 | 0.00287581 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3814054 | TTTCCAAAGACAGCA[C/T]CATGTATACCATTTA | 57097 |
rs767358251 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3826349 | GGAGCTTCGGGAGTA[A/G]CTGGCAAGCATAGTG | 57097 |
rs767408832 | snp | C/T | 6.62998e-05 | 0.00575721 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812403 | TCATCTTTGCAGAAA[C/T]GACTGGAATAAGCAG | 57097 |
rs767455889 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3827864 | CTCACAGGAATTGAG[A/C]AAGAACAGCTAAAGG | 57097 |
rs767466606 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3852274 | CGGAACAAAGCTGGA[G/T]GGAGAATGACTTTGA | 57097 |
rs767486434 | snp | A/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3814610 | TCCTCAGAAACTAGA[A/T]AATGTTGGTTCAGTT | 57097 |
rs767490140 | in-del | -/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3867036 | ACTTTTTGTTCTACA[-/T]TATCAGTGAAAACTT | 57097 |
rs767509790 | snp | G/T | 1.64953e-05 | 0.00287182 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3829977 | ATCCACTTCATTGTT[G/T]GTTGTTTTAGAAAAT | 57097 |
rs767573475 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3841905 | TTCCACAGTAGATGA[A/G]TTTCCAGCAGCCAGG | 57097 |
rs767675997 | in-del | -/AGAAGGAAG | | | cds-indel, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810646 | GAGGGAGGGAGGGAA[-/AGAAGGAAG]GAAGGAAGGAAGGAA | 57097 |
rs767835216 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3856383 | CATCTGACAAAGGGT[G/T]AATATCCAGAATCTA | 57097 |
rs767886460 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3830667 | TAGTAACCTTTATAT[C/T]ACTTACTACGTGCCA | 57097 |
rs767896254 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3812950 | TGGGATTACAGGCGC[G/T]TGCCACCACACCCAA | 57097 |
rs767970764 | snp | C/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3820716 | AAGTCAAAGGAGGCA[C/G]AGGCTTCTGTCTTCC | 57097 |
rs767983387 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3850291 | AGACATAATATATAT[A/C]GCATAATTATATCAG | 57097 |
rs768085105 | snp | C/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3846684 | ATGGCGTGAACCCAG[C/G]AGGCAGAGCTTGCAG | 57097 |
rs768089545 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3855886 | AAACTATACTAAAAG[A/G]CTACAGTAACCAAAA | 57097 |
rs768168130 | snp | C/T | 1.66607e-05 | 0.00288619 | intron-variant | PARP11 | GRCh38.p7 | 12:3828893 | AAAACACACAACTAT[C/T]AGGGAAAAAAACATA | 57097 |
rs768225055 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3860794 | TGATCCTTGTGCTTC[A/G]GCTTCCTGAGGAGCT | 57097 |
rs768260458 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812000 | TTTATATGGAGGCCA[A/C]TTTTTTTCATATCTG | 57097 |
rs768279797 | snp | A/C | 5.03326e-05 | 0.00501635 | intron-variant | PARP11 | GRCh38.p7 | 12:3828870 | GATTTTATCATATCA[A/C]TATACTAAAAACACA | 57097 |
rs768332783 | snp | C/G | 1.69441e-05 | 0.00291063 | intron-variant | PARP11 | GRCh38.p7 | 12:3826245 | ATTTCTGTATACAAA[C/G]ACAAGATATTAGATA | 57097 |
rs768488650 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3859894 | GGTTACTCCAACATA[A/G]AGATGTAACAGTTAT | 57097 |
rs768489108 | snp | C/G | | | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3874466 | TTTTCGCCATGTTGG[C/G]CAGGCCAGTCTCGAA | 57097 |
rs768495643 | snp | C/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3833320 | TTAAAAACTAGTAGG[C/G]CGGGCGTGGTAGCTC | 57097 |
rs768528672 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3832756 | ATATTCACCAGTTAT[C/T]GGTTATGAAGCAGGT | 57097 |
rs768617398 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3818870 | TTCTGTGGTTGTCAG[C/T]TTCCTCCTTGGGTTT | 57097 |
rs768675666 | snp | A/G | 1.64944e-05 | 0.00287175 | intron-variant | PARP11 | GRCh38.p7 | 12:3829048 | TTAAGACAAACCAGA[A/G]AGTTTCATTTACCAG | 57097 |
rs768768098 | snp | C/T | 1.64857e-05 | 0.00287099 | intron-variant | PARP11 | GRCh38.p7 | 12:3822038 | TAGATTTACTGCAGT[C/T]ATTTCCGGTTTCTTT | 57097 |
rs768779447 | in-del | -/T | 1.65464e-05 | 0.00287627 | frameshift-variant, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3814163 | TCTGAGGCACACCTC[-/T]TTTTTTCTTGAGCTG | 57097 |
rs768817006 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3856279 | ATAGACAAATGGGAT[A/C]TAATTAAAGAGTTTC | 57097 |
rs768845285 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3849940 | TGTCCTGAAAATATG[C/T]ATATCGATTATGTAT | 57097 |
rs768911034 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3811126 | GTCAACAGCTACTTC[-/A]AAGGAGAAACCAGAT | 57097 |
rs768912159 | in-del | -/AC | | | intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3872146 | GGAGGAAGAAATGAT[-/AC]ACAGAGAGGCCAAGA | 57097 |
rs768950978 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3864305 | TCATGATGTATTAAT[A/C]CTTTTATATATGTTA | 57097 |
rs769023310 | snp | A/T | 1.66405e-05 | 0.00288443 | utr-variant-5-prime, missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3830015 | CTGCTTTGTGAAACA[A/T]CTCCTGAAAAGCCAG | 57097 |
rs769038673 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3851131 | AAAAGATACAGCATT[A/G]GGGGTCCATTCCAAG | 57097 |
rs769073474 | in-del | -/CT | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3809305 | TTTAACATCCATTAA[-/CT]CTGTACTATCATATT | 57097 |
rs769205328 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3825297 | TCAGACTTCTTATGG[A/C]CAGAGCAAGCAAAAA | 57097 |
rs769208780 | snp | C/G | 1.64751e-05 | 0.00287007 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3829941 | AAACCAGCCCCACTG[C/G]GTATCTGACGTGTCC | 57097 |
rs769212149 | snp | C/T | 0.000108635 | 0.00736923 | intron-variant | PARP11 | GRCh38.p7 | 12:3812474 | GAAAAGCCAAGATTA[C/T]TCCGAAGAATATATT | 57097 |
rs769234197 | snp | C/G | 1.64776e-05 | 0.00287028 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812325 | ATAGATTTATATGTT[C/G]TAAACAGATGCCGCT | 57097 |
rs769241741 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3814304 | GGAAATACTTTAATA[C/T]AAATAACAAGTGGAC | 57097 |
rs769330716 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3830134 | GTCTTTCCTCCCATG[A/G]CACTTTAAAAACAGC | 57097 |
rs769333662 | in-del | -/G | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810171 | CTAAGAAGTTAAATT[-/G]TGTACACTAACTCTC | 57097 |
rs769437884 | snp | A/G | 1.64912e-05 | 0.00287147 | synonymous-codon, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812180 | ATCAAAAACCACAAA[A/G]ATCTTTGGGTTCCAG | 57097 |
rs769446842 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3809296 | AAATAAAATTTTAAC[A/G]TCCATTAACTCTGTA | 57097 |
rs769468059 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3831299 | TATACACACATAAAA[A/C]CATATAGAGTTATTG | 57097 |
rs769508712 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3846433 | AAATTCCTGGACATA[C/T]AGAATCTACTATGAT | 57097 |
rs769572744 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3846366 | ACAAAGAATTATTAG[A/G]GACTATTATGGACAA | 57097 |
rs769646191 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3822434 | AAACCCCGTCTCTAC[C/T]AAAAATACAAAAAAA | 57097 |
rs769687921 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3823847 | CTTGAACCTGGGAGG[C/T]GGAGGCTGCAGTGAG | 57097 |
rs769777077 | snp | C/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3844371 | CCATTTCTTTCTTAA[C/G]ACTGGTGGCTCAGTT | 57097 |
rs769781506 | snp | A/G | 1.66023e-05 | 0.00288113 | intron-variant | PARP11 | GRCh38.p7 | 12:3822171 | AACTTGAAACAGCAA[A/G]AGAGAAAACAAAATA | 57097 |
rs769924235 | snp | A/G | 1.69404e-05 | 0.00291031 | intron-variant | PARP11 | GRCh38.p7 | 12:3830036 | GAAAAGCCAGAAGGA[A/G]GTGGAGGAAGAAATA | 57097 |
rs769947628 | snp | G/T | | | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839614 | TGGGTAGGACAAATG[G/T]AAATAAGTGCCCTTT | 57097 |
rs769972983 | snp | A/G | 3.29533e-05 | 0.00405901 | utr-variant-5-prime, missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3829951 | CACTGGGTATCTGAC[A/G]TGTCCATGTCATCCA | 57097 |
rs770001883 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3862008 | CCAACCTGGTTGATG[A/G]AGCGAGACTCCGTAC | 57097 |
rs770076098 | in-del | -/AGG | 1.66164e-05 | 0.00288235 | intron-variant | PARP11 | GRCh38.p7 | 12:3821842 | AAAGACATAGTGGAA[-/AGG]AGAAGTTTCAGATTA | 57097 |
rs770094973 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3838971 | GGCGACCCCCGGCCT[G/T]GGTCCTGAGTCGGGC | 57097 |
rs770106270 | in-del | -/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3850475 | CAAGGGAAAAAAGAC[-/T]TTTCCCAGGCCCTTT | 57097 |
rs770140883 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3812529 | AGGAGAATAGATGCA[C/T]AGAATTGTATAATAA | 57097 |
rs770153529 | snp | C/T | 1.6513e-05 | 0.00287336 | synonymous-codon, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3814155 | TTCATTAATCTGAGG[C/T]ACACCTCTTTTTTTC | 57097 |
rs770205786 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3867731 | AAGAACATGACTAAA[G/T]GTTAAAACAAAACAT | 57097 |
rs770249667 | snp | A/C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3841270 | GATAAGAATATTCTT[A/C/T]GATTCTTCTTCAATC | 57097 |
rs770339961 | snp | C/T | 1.90424e-05 | 0.00308558 | intron-variant | PARP11 | GRCh38.p7 | 12:3812488 | ACTCCGAAGAATATA[C/T]TAAAAACAAGCAAAA | 57097 |
rs770345356 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3852453 | CTTAAATGACCTGAT[A/G]GAGCTGAAAACCATG | 57097 |
rs770379219 | snp | A/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3827665 | TAACTCTTGATAATT[A/T]AAAAAAAAAGCAAGA | 57097 |
rs770428348 | snp | A/G | | | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3870481 | AAATCAAGTATATAA[A/G]ACATTCATTAATGCC | 57097 |
rs770586006 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3821562 | GACTTCTAATAAAAG[G/T]CTTAGCCAAGGAAGT | 57097 |
rs770647917 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3842890 | TGCTTTATAGTGCTT[A/C]CTAAAGTGACAAGAA | 57097 |
rs770716873 | snp | A/G | 6.59e-05 | 0.00573983 | stop-gained, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812299 | CTCCAATTAGCACTC[A/G]AGCAAGAAACATAGA | 57097 |
rs770741862 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3844164 | CTGCTGATTTGAGTA[G/T]TGATTAGCATTTAGA | 57097 |
rs770763962 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3833561 | GTGAGCTAACATCAC[A/G]CCACTGCACTCCAGC | 57097 |
rs770777230 | snp | A/C | 5.02913e-05 | 0.00501429 | intron-variant | PARP11 | GRCh38.p7 | 12:3822192 | AAACAAAATATCAGA[A/C]GCCGATTACAATTAC | 57097 |
rs770783605 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3830438 | TTTCATTTAATGGCA[C/T]AGAAAGATATTTATA | 57097 |
rs770853161 | snp | C/T | 6.65757e-05 | 0.00576918 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3826197 | GCTCTTTTTATTAAG[C/T]GCTGCTTTCCAGTGG | 57097 |
rs770915780 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3858284 | AAAATAATTAAAATG[G/T]TTCTGAATCAAGGTG | 57097 |
rs770929878 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3868038 | ATTTAGTAGACATAC[A/G]GAGTAATCAAAATGT | 57097 |
rs771057709 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3818160 | GACAGAAATCCTGTG[A/G]TTCCCAAGACAGCTC | 57097 |
rs771057789 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3841364 | AGGCCTACCTGGCAG[C/T]CTGCAGGATGTACCC | 57097 |
rs771062986 | snp | G/T | 3.32519e-05 | 0.00407736 | synonymous-codon, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3814173 | ACCTCTTTTTTTCTT[G/T]AGCTGAGCCTTTTTC | 57097 |
rs771080727 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3866235 | GTTTATCCTCTGTCC[C/T]GAATAACTCTTCTCT | 57097 |
rs771108036 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3831725 | AAGAAATGAAAAATA[G/T]AACACCCTAGGATCA | 57097 |
rs771128594 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3864913 | TTCCACTCTAACCTT[C/T]ATTTCCTTGCTCCTG | 57097 |
rs771175386 | snp | A/G | 0.000238152 | 0.0109096 | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3873202 | CGCCCCGTCCCGCCC[A/G]GCTACTCACTGGATT | 57097 |
rs771181936 | snp | C/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3817753 | TGCTCTGCACTGGAG[C/G]AAGAATACTTTCATG | 57097 |
rs771212735 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810539 | AGGTTGCAGTGAGCC[G/T]AGATCACACCACTGC | 57097 |
rs771255734 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3816212 | TTTAAATTAAAAAAA[G/T]AAGATAATACTTGTT | 57097 |
rs771506787 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3833401 | AGGCCAGGAGTTTGA[A/G]GCAAGCCTGGCAACA | 57097 |
rs771533969 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3858205 | GTAAGCTGGAAGAAG[C/T]GAATATCAAAGATGT | 57097 |
rs771539942 | snp | A/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3849830 | GAATAGTTTGAATGG[A/T]TTCTAGCATAAAGAA | 57097 |
rs771634874 | snp | A/T | 1.67075e-05 | 0.00289023 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3826217 | CTTTCCAGTGGTGAG[A/T]TTCATTTGCTTCATT | 57097 |
rs771642667 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3848227 | GTTAAAATGACAATA[C/T]TGCCCAAAGCAATTT | 57097 |
rs771658091 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3827583 | TCAGGGCCTCTTAAA[C/T]CCTGCTTATTTGCCT | 57097 |
rs771668498 | in-del | -/AGAGAG | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810736 | AAGAGAAAGAGAAAG[-/AGAGAG]AGGAAGAGAAAAAGG | 57097 |
rs771687983 | snp | C/T | 1.75727e-05 | 0.00296412 | intron-variant | PARP11 | GRCh38.p7 | 12:3826107 | TGTTTTTCTGTCCAA[C/T]AGTAAGAAAAAAAAA | 57097 |
rs771753451 | snp | G/T | | | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812238 | TTCACATAGCTCCCG[G/T]CTTTGGAAGGAGGTC | 57097 |
rs771820518 | snp | C/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3860943 | TCAGCCTGCCAGGTA[C/G]CTGGGATTACAGGCA | 57097 |
rs771835701 | in-del | -/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3823580 | CGCCATGTGGATACA[-/C]CCATAATAATATTTA | 57097 |
rs771912600 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3846842 | ATAATCCCAGCACTT[C/T]GGGAGGCTGAGGTAG | 57097 |
rs771976427 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3868769 | TCACCTTCGTCTCTA[C/T]CCTGGACTACACTAT | 57097 |
rs772066188 | snp | A/G | | | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3870355 | GAGATGATCTGTGGA[A/G]GATTCCCCACTTTTA | 57097 |
rs772093185 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3816322 | TTGAATCCCTCACAA[A/G]TGTGATAAGCAAGCC | 57097 |
rs772095127 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3843588 | AGTTCTTTTCTAGAG[A/G]ATGCTGCTAGAAAAT | 57097 |
rs772132360 | snp | C/T | 1.65012e-05 | 0.00287234 | synonymous-codon, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3821926 | CTGAATTCTTTTAAT[C/T]CGGTTGCGATCCATC | 57097 |
rs772150146 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3818343 | ACCTAACTCCTCTTT[C/T]CGTCCTCTACCTCTA | 57097 |
rs772258063 | in-del | -/A | | | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3870172 | AAGCGAAACTAAAAT[-/A]AACTAACAAATTACT | 57097 |
rs772339299 | snp | A/G | 1.71616e-05 | 0.00292925 | intron-variant | PARP11 | GRCh38.p7 | 12:3814204 | CTAAAAACACAATAT[A/G]CACAGACACAAAAGC | 57097 |
rs772356592 | snp | A/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3851787 | AGTGTTTGAGCTCCA[A/T]GAATGGACAGACTGC | 57097 |
rs772384248 | snp | C/T | 1.64806e-05 | 0.00287054 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812200 | TTGGGTTCCAGGTAT[C/T]ATCCACACAGCTGTC | 57097 |
rs772523908 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3809043 | TTTACCCTGAGGCTG[A/G]TATCACCAAGGTGAA | 57097 |
rs772600557 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3864787 | ATTGGTAATTTGTGT[C/T]TTCTTTTTCTCCTGA | 57097 |
rs772627223 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3851309 | GAAGGGCAGGGCATC[A/G]CCTCACCCAGGAAGC | 57097 |
rs772632316 | snp | A/T | 1.64806e-05 | 0.00287054 | synonymous-codon, missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3829891 | AGGAAAGGAGGTACC[A/T]GAAACATGTGCCACT | 57097 |
rs772667082 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3816846 | GGCGGAGGTTGTAAT[A/G]AGCTGAGATTGTGCC | 57097 |
rs772681438 | snp | C/T | 1.64846e-05 | 0.0028709 | intron-variant, splice-acceptor-variant | PARP11 | GRCh38.p7 | 12:3829031 | ACTGTTGGTATCCGG[C/T]TTTAAGACAAACCAG | 57097 |
rs772706763 | in-del | -/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3835300 | TAAGAGGGGAAAAGT[-/C]CTGAGCTGGGATATC | 57097 |
rs772734766 | in-del | -/CTT | | | intron-variant | PARP11 | GRCh38.p7 | 12:3864934 | CTTGCTCCTGTTTAA[-/CTT]CTTCTTTTTCCAGTT | 57097 |
rs772738217 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3861942 | AGACAGGAGAATGGC[A/G]TGAACCCAGGAGGCA | 57097 |
rs772768302 | snp | C/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3868790 | ACTACACTATAACCT[C/G]CTAATTAGTCTTCCT | 57097 |
rs772828697 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3843352 | GTCAGAACTGCAGAA[A/G]TTTTCTAAATGCCAC | 57097 |
rs772924037 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3841878 | GGATCTGTCTAAAGA[C/T]TGTGGTTCAGTTTCC | 57097 |
rs772941686 | snp | C/T | | | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3875088 | TACTTGTTTTCTGTA[C/T]CTTTAGATGCATTAA | 57097 |
rs772950121 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3844488 | TTTTGATAGAAACAC[C/T]AGATTTGAAAGTTCA | 57097 |
rs772994930 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3846865 | TGAGGTAGGAGGATC[A/G]TTTATGGCCAGGAGT | 57097 |
rs773013388 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3832918 | TTCAAGGGCAATGGG[C/T]ATGCTGGTAGAGCCT | 57097 |
rs773028014 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3821515 | ACTATTGGCAAGATA[A/G]TATGATTTAAAAACA | 57097 |
rs773067923 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3854320 | TAGAGGCACAAAAAA[C/T]TCTTCAAAAAAACAA | 57097 |
rs773069805 | snp | G/T | | | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3870473 | GATATAACAAATCAA[G/T]TATATAAGACATTCA | 57097 |
rs773126094 | snp | A/T | 1.70545e-05 | 0.0029201 | intron-variant | PARP11 | GRCh38.p7 | 12:3813991 | CCTCTAAAAAGAGGA[A/T]ACTCTCTCCTGGGGC | 57097 |
rs773171754 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3824345 | TGAATAAAAATATTT[A/C]CCCAATTTTCTGTGA | 57097 |
rs773203945 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3863380 | TTTTCCTTAGAACCT[C/T]TAGTAGAATACTGAA | 57097 |
rs773297018 | snp | A/G | 1.69919e-05 | 0.00291473 | intron-variant | PARP11 | GRCh38.p7 | 12:3830040 | AGCCAGAAGGAGGTG[A/G]AGGAAGAAATAATTC | 57097 |
rs773324334 | snp | C/T | 1.64798e-05 | 0.00287047 | intron-variant | PARP11 | GRCh38.p7 | 12:3822064 | TCTTTCATGGGTATA[C/T]TCAGTCAATTCTGCT | 57097 |
rs773356131 | snp | C/T | 3.29685e-05 | 0.00405995 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812358 | TGCAAGCTGACACCA[C/T]GAATTTGGAATGTGT | 57097 |
rs773375522 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3815368 | GCCTTCTGTTACTTC[C/T]ATTGATTGGTCTTAG | 57097 |
rs773407266 | in-del | -/AC | | | intron-variant | PARP11 | GRCh38.p7 | 12:3836024 | ATTTTATATATATAT[-/AC]ACACACACACATATA | 57097 |
rs773470758 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3842634 | CCTCTCCCCAGCCTC[C/T]TTACCTTCCCTCCCA | 57097 |
rs773489201 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3830334 | CAAGCATTTTCAATT[C/T]TATCTTATGCTCATG | 57097 |
rs773491295 | snp | A/G | 1.64765e-05 | 0.00287019 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3829953 | CTGGGTATCTGACGT[A/G]TCCATGTCATCCACT | 57097 |
rs773515479 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3863399 | TAGAATACTGAATAA[A/C]GAATGGACATCATTG | 57097 |
rs773526108 | in-del | -/ATT | 6.63967e-05 | 0.00576142 | intron-variant | PARP11 | GRCh38.p7 | 12:3821856 | AAGGAGAAGTTTCAG[-/ATT]AGAAATCATCTCACC | 57097 |
rs773526341 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3837667 | GGCTGAATGGCGAAG[A/G]AAAAAAAAAACCAAG | 57097 |
rs773571661 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3814474 | CATAAAGGTAATTGA[C/T]TGTCTAAACCAGCTA | 57097 |
rs773587263 | in-del | -/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3832546 | CTTCACAGATGCTCT[-/G]GGTTTCTTTAAAAAG | 57097 |
rs773600488 | snp | A/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3814410 | CACTGAAACTTAAGG[A/T]TGAAAATTATGCCAA | 57097 |
rs773652945 | snp | C/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3852655 | ACCAAATCTATGTTT[C/G]ATTGGTGTACCTGAA | 57097 |
rs773680122 | snp | C/G | | | intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3872219 | TTTATTAACATTAGA[C/G]TATATCCTTTGTCCA | 57097 |
rs773704348 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3851318 | GGCATCGCCTCACCC[A/G]GGAAGCACAAGGGAT | 57097 |
rs773712053 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3827822 | ACCCAGCCACAATAC[A/G]CTACTAACACTGTCA | 57097 |
rs773726497 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3836516 | TACTAGGCATTCGTA[A/G]TAATCCATGGGGGAT | 57097 |
rs773739101 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3856109 | TTCCTTACACCTTAT[A/G]TAAAAATTAATTTTC | 57097 |
rs773746009 | snp | C/T | 1.64757e-05 | 0.00287012 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3822086 | AATTCTGCTCTTACC[C/T]GATATGGTACTTGAG | 57097 |
rs773776926 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3832120 | ACACCTTACCTAAGA[C/T]TTCGCTTTAGGCCAG | 57097 |
rs773803061 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3847139 | ATAAAGAAAATTAAA[A/C]CTAAGCAAACCAACA | 57097 |
rs773915134 | in-del | -/CAGAAAC | | | intron-variant, nc-transcript-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3871933 | CCCAGAAGTGAGTCA[-/CAGAAAC]CAGAATTCTTCCCCA | 57097 |
rs773955924 | in-del | -/AAGAGA | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810721 | AGAGAAGAGAAGAGA[-/AAGAGA]AAGAGAAAGAGAAAG | 57097 |
rs773964941 | snp | C/T | 0.000472757 | 0.0153673 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3873271 | GCCTGTGGGAAGGGG[C/T]TAGCCGCGGGGCCTG | 57097 |
rs774029649 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3809429 | GGTATAGTACCTTCT[C/T]ACAATGGCTACTGCA | 57097 |
rs774187319 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3868570 | TCATAGGCACATTAA[A/G]CATAGTGAGTCCAGA | 57097 |
rs774273774 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3818751 | TCAAATTTATCTTAC[C/T]TGACATCTTTTCAGT | 57097 |
rs774284673 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3866682 | CACAAAGCACAAAGT[A/C]CATTTGCTTTGTTAA | 57097 |
rs774300495 | in-del | -/A | | | intron-variant | PARP11 | GRCh38.p7 | 12:3868144 | CTTCTCAATGATAAT[-/A]AAAACATTAATTTCT | 57097 |
rs774335959 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3832822 | ACAATGCCATATCCT[A/G]TCTGATTTTCCTGTT | 57097 |
rs774471517 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3862235 | TTTAGACTAGATCAC[C/T]TGAAGTCAGTAGTTT | 57097 |
rs774473886 | in-del | -/A | | | intron-variant | PARP11 | GRCh38.p7 | 12:3841369 | TACCTGGCAGCCTGC[-/A]GGATGTACCCAAAGG | 57097 |
rs774536680 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3829275 | ATATATATAGAAATA[C/T]AGTTATTTTTCCAGA | 57097 |
rs774543070 | snp | C/T | 0.000116884 | 0.00764384 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3814177 | CTTTTTTTCTTGAGC[C/T]GAGCCTTTTTCCTAA | 57097 |
rs774594374 | snp | A/G | 1.67781e-05 | 0.00289634 | intron-variant | PARP11 | GRCh38.p7 | 12:3814028 | TGGACCTGGAATTCT[A/G]ATAATTACCTTTTCC | 57097 |
rs774693602 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3814308 | ATACTTTAATATAAA[C/T]AACAAGTGGACAAAG | 57097 |
rs774752837 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3832572 | AAAAGATGCATTTTA[C/T]AAGATTAAACATTTC | 57097 |
rs774817364 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3835255 | GTACATAGTCTATGC[A/C]AATCCAGAAATGCCA | 57097 |
rs774823239 | in-del | -/A | 0.0122028 | 0.0771523 | intron-variant | PARP11 | GRCh38.p7 | 12:3826113 | CTGTCCAATAGTAAG[-/A]AAAAAAAAAACCCAC | 57097 |
rs774860049 | snp | A/C/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3850071 | CAAGAAGGCAGGTGG[A/C/G]AACAAAGCTATATTG | 57097 |
rs774915860 | in-del | -/TTC | | | intron-variant | PARP11 | GRCh38.p7 | 12:3838813 | CGAAAGGCCGCGTCT[-/TTC]TTTTTTGGTTTCCTC | 57097 |
rs774926294 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3825179 | CTTGCTTGAAGAGTC[A/C]TTTTAGAAAATAGGA | 57097 |
rs774993484 | in-del | -/AAAG | | | intron-variant | PARP11 | GRCh38.p7 | 12:3847368 | AAGGACACAACAAAC[-/AAAG]AAAACCATAGGCCAA | 57097 |
rs775107533 | snp | C/T | 1.67888e-05 | 0.00289726 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3826228 | TGAGATTCATTTGCT[C/T]CATTTCTGTATACAA | 57097 |
rs775108062 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3852220 | CTAAAAACCAGAGCA[C/T]CTCTTCTCCTCCAAA | 57097 |
rs775113963 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3859821 | AATGCCAGGCAAAAT[A/C]GACTTCAAACCAAAA | 57097 |
rs775160532 | snp | A/T | 2.49237e-05 | 0.00353004 | intron-variant | PARP11 | GRCh38.p7 | 12:3826114 | CTGTCCAATAGTAAG[A/T]AAAAAAAAACCCACT | 57097 |
rs775183442 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3827629 | AAAATGGCTTGTCAC[A/G]AGCAAGGATCTAATG | 57097 |
rs775191591 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3821811 | AATACAATTCAATAT[G/T]TATGTTTTAACCATA | 57097 |
rs775223154 | snp | A/G | | | intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3872113 | CCCTCATTCCAGAAG[A/G]GACCTTCCTCCTCCG | 57097 |
rs775229718 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3817227 | TCACTACTTTTCGGG[A/C]ACAAATTCGATTGAA | 57097 |
rs775291106 | snp | C/T | | | downstream-variant-500B | PARP11 | GRCh38.p7 | 12:3808437 | GAACGGAATGTTTAA[C/T]TCAGTTCAACAGGAA | 57097 |
rs775358304 | in-del | -/GA | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810619 | AGAAAAAGAAAAAGG[-/GA]GAGGAGGGAGGGAGG | 57097 |
rs775406519 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3843644 | GTTACCCTTAGGTAG[A/G]TAACATCTTCCATTC | 57097 |
rs775490422 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3844500 | CACCAGATTTGAAAG[G/T]TCAATGTGTTTGATC | 57097 |
rs775571728 | in-del | -/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3837523 | ACCAGAAAGGAAGAT[-/G]TAAGAAAGGAAGAGA | 57097 |
rs775602412 | in-del | -/GTTCA | | | intron-variant | PARP11 | GRCh38.p7 | 12:3818529 | CTTTCCAATTACAAT[-/GTTCA]GTTCTCTCCCATGAT | 57097 |
rs775661386 | snp | A/C/G | 8.31779e-05 | 0.00644848 | intron-variant | PARP11 | GRCh38.p7 | 12:3828898 | ACACAACTATTAGGG[A/C/G]AAAAAACATACCTGC | 57097 |
rs775671755 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3818600 | TTAGCTGTCTTCTCA[C/T]ATCTCTCATCCTCCT | 57097 |
rs775748994 | snp | A/T | | | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839615 | GGGTAGGACAAATGG[A/T]AATAAGTGCCCTTTC | 57097 |
rs775797593 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3861227 | AGGGCCAGAATGTTA[C/T]AGACTAAACGTTTGT | 57097 |
rs775803427 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3837866 | GATAAAGAAGGTCAA[C/T]AAATAATGATAATGG | 57097 |
rs775827919 | snp | G/T | 1.64977e-05 | 0.00287203 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3821930 | ATTCTTTTAATTCGG[G/T]TGCGATCCATCGTCT | 57097 |
rs775869109 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3812542 | CATAGAATTGTATAA[C/T]AAAAATAGATGTGGA | 57097 |
rs775879028 | snp | A/G | 3.3145e-05 | 0.0040708 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3814048 | TTACCTTTTCCAAAG[A/G]CAGCACCATGTATAC | 57097 |
rs775926730 | snp | A/G | 3.29506e-05 | 0.00405884 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812301 | CCAATTAGCACTCGA[A/G]CAAGAAACATAGATT | 57097 |
rs775970961 | snp | A/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3848415 | TCAAAATATACTACA[A/T]AGCTATAGTAATCAA | 57097 |
rs775985089 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3832757 | TATTCACCAGTTATC[A/G]GTTATGAAGCAGGTA | 57097 |
rs776066856 | snp | C/T | 1.64754e-05 | 0.00287009 | intron-variant, missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3828988 | TTTTGAAGCTTTTTT[C/T]GATATCTTCACTGCT | 57097 |
rs776174999 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3830102 | TTTTACTTCTTTACA[A/C]AGAGTGGTATTCAAG | 57097 |
rs776180497 | snp | A/G | 1.64895e-05 | 0.00287132 | intron-variant | PARP11 | GRCh38.p7 | 12:3829040 | ATCCGGCTTTAAGAC[A/G]AACCAGAAAGTTTCA | 57097 |
rs776186682 | snp | C/T | 6.70905e-05 | 0.00579144 | intron-variant | PARP11 | GRCh38.p7 | 12:3828871 | ATTTTATCATATCAA[C/T]ATACTAAAAACACAC | 57097 |
rs776240011 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3821738 | GAATGCTGAAGAGCC[C/T]TGAGACCAGGTCAAA | 57097 |
rs776306112 | in-del | -/CATG | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3809775 | GAACGGGTTTAGAGC[-/CATG]CATGGTATGCTGCCT | 57097 |
rs776355118 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3844121 | TTATTTACCTCTGTG[C/T]TGTTTTAATTACCTA | 57097 |
rs776437496 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3820140 | CTGGCTCTCCAAGCT[A/G]TGGTTCTCTGTACCA | 57097 |
rs776447500 | snp | A/G | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3873129 | CTGAAGCGAGCGCGG[A/G]GAAGCAGTTCCGGTG | 57097 |
rs776482337 | snp | A/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3858305 | AATCAAGGTGATTTG[A/T]TAACAGTGATAAAGA | 57097 |
rs776546428 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3841989 | AGGCCGGACAGAGCA[A/G]TCTTCCCAGACACGA | 57097 |
rs776570727 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3842924 | ACACCATTTGACACA[A/C]TATAGATTCCAAACA | 57097 |
rs776584439 | snp | C/T | 1.64963e-05 | 0.00287192 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3821937 | TAATTCGGTTGCGAT[C/T]CATCGTCTTCCCAAA | 57097 |
rs776720610 | in-del | -/TATACCATAAGTAGCATTTAT | 1.77354e-05 | 0.00297781 | intron-variant | PARP11 | GRCh38.p7 | 12:3814229 | AAAAGCACACAGAAA[-/TATACCATAAGTAGCATTTAT]TAATCTTAATGAGCA | 57097 |
rs776778536 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3809215 | AGTATTATTATATAC[C/T]GGTTATATAATTCTC | 57097 |
rs776784718 | snp | A/G | 1.65059e-05 | 0.00287275 | intron-variant | PARP11 | GRCh38.p7 | 12:3829066 | TTTCATTTACCAGCT[A/G]TTCACATTAATGACT | 57097 |
rs776811750 | snp | C/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3836753 | TGCAAATATTATGTA[C/G]GGAGAGACAGTTCCC | 57097 |
rs776880722 | in-del | -/C | | | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3874204 | ACCTGATTTTTTTTT[-/C]ACTTTAAAGATTATG | 57097 |
rs776897724 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3831856 | CACAATTCCTACTGC[G/T]TTTTTTTATTAATGT | 57097 |
rs776906351 | in-del | -/CT | | | intron-variant | PARP11 | GRCh38.p7 | 12:3836883 | ACAGAAAACTTTCCC[-/CT]GATTCATGATTTCTA | 57097 |
rs776929867 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3865177 | AATCTTTCTGTTACT[A/G]GTTTCTAACTTAATT | 57097 |
rs776931096 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3810649 | GGAGGGAGGGAAAGA[A/G]GGAAGGAAGGAAGGA | 57097 |
rs776938570 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3851468 | TTATATCCCGCACCT[G/T]GCTCAGCGGGTCCCA | 57097 |
rs776939472 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3827483 | CATATCATTCGGTTT[C/T]AGTTCTTCCTCAAAA | 57097 |
rs776991114 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3837788 | TTGGAAAACAAAGAA[A/G]AGCAAAGAGTAGCTA | 57097 |
rs777047930 | snp | C/T | 3.2956e-05 | 0.00405918 | synonymous-codon, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812336 | TGTTCTAAACAGATG[C/T]CGCTGTTGCAAGCTG | 57097 |
rs777086765 | snp | A/C/G | 6.85981e-05 | 0.00585619 | intron-variant | PARP11 | GRCh38.p7 | 12:3812443 | CAAAATAGGTTCCTT[A/C/G]AACAAAGAGGACCAA | 57097 |
rs777106406 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3861070 | ACCTTGGGCTCAACT[A/G]CATCTGATTTAGATA | 57097 |
rs777127461 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3825673 | AGCACTTAGAGTAAA[C/T]AATAATGTTGCTATT | 57097 |
rs777184828 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3864131 | TTCCTAGGCTGCTGA[A/G]AATTTTAATCAGGAA | 57097 |
rs777189680 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3811231 | ATCATTGTTGAATAG[A/C]TGTGTGTGCTGCAGA | 57097 |
rs777246753 | in-del | -/A | | | intron-variant | PARP11 | GRCh38.p7 | 12:3814320 | AAATAACAAGTGGAC[-/A]AAGCAAGTCTAGAAA | 57097 |
rs777380303 | snp | A/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3849504 | ATGACATTGGCAGCA[A/T]CATGGATGAAATGAG | 57097 |
rs777472005 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3813713 | AATGTACATCCCATA[A/C]CTTTTCCCCTCACCT | 57097 |
rs777477292 | snp | G/T | 1.64757e-05 | 0.00287012 | synonymous-codon, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812285 | TCCGTTTATGTAATC[G/T]CCAATTAGCACTCGA | 57097 |
rs777556914 | snp | C/T | 1.66524e-05 | 0.00288547 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3826185 | ATAGAAAAGGGGGCT[C/T]TTTTTATTAAGCGCT | 57097 |
rs777666861 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3831632 | GTTTGTTATTTTTTA[C/T]ATATGTTTGGAAACT | 57097 |
rs777814557 | in-del | -/AC | | | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3840799 | GATGATAAATATGCA[-/AC]AGTTTCATCACCATC | 57097 |
rs777846017 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3851730 | GCAGACTTAAATGTC[C/T]GTGTCTGACAGCTCA | 57097 |
rs777861048 | snp | A/C | | | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3871529 | GGCTTATGAAAGTAC[A/C]CTCTATGACGTTGGC | 57097 |
rs777863333 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3844087 | GGCTCAGTGAATCGC[C/T]ACTGTACTGTAATAA | 57097 |
rs778025946 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3808897 | ATCATCACATGTAAA[A/C]GCAATACATTCATAT | 57097 |
rs778137845 | snp | A/G | 1.66214e-05 | 0.00288278 | intron-variant | PARP11 | GRCh38.p7 | 12:3821838 | CATAAAAGACATAGT[A/G]GAAAGGAGAAGTTTC | 57097 |
rs778158621 | snp | C/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3867338 | GAAATGGCAGCGTTT[C/G]CAAGATTATTCTTCC | 57097 |
rs778205984 | in-del | -/AAAAGT | | | intron-variant | PARP11 | GRCh38.p7 | 12:3821168 | CAATTTCTCTGAATA[-/AAAAGT]AAAAGTTAAAAGTCA | 57097 |
rs778317735 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3813423 | CGATAAAGCAGCCAA[C/T]TCTTCTGAAATGGTA | 57097 |
rs778337693 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3828218 | TATTGCCAGCTACCT[A/G]TGACTTTCTCACTTA | 57097 |
rs778342777 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3866154 | GGATGTCTAATGAGC[C/T]TCACATTACTAAATC | 57097 |
rs778344629 | in-del | -/TACC | | | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3874173 | AATGTAATCAAAGAA[-/TACC]TATAGATTTAGAACC | 57097 |
rs778392798 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3816860 | TGAGCTGAGATTGTG[C/T]CACCGCACTGCAGCC | 57097 |
rs778394236 | snp | C/T | | | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3814162 | ATCTGAGGCACACCT[C/T]TTTTTTTCTTGAGCT | 57097 |
rs778422241 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3815502 | ATTCCTTCAACCACT[C/T]CTGACACAGCATAGC | 57097 |
rs778424734 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3813798 | AACATTATAAATAAC[A/G]TGAAGTTTTCCCCCA | 57097 |
rs778430485 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3851894 | ACAGTCGGATGCCCC[C/T]CTGAGACGAAGCTTC | 57097 |
rs778607232 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3861704 | CTTTTTTTTTTCATC[A/G]ATCATAGTCCTGGCA | 57097 |
rs778659120 | snp | C/T | | | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3840433 | CCATTAGCACTACCT[C/T]CTCGACTGCAGCATC | 57097 |
rs778707249 | snp | C/T | 1.64852e-05 | 0.00287094 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3814097 | AGTTATGAATGCAGA[C/T]TGCTTCCACAAATTC | 57097 |
rs778723382 | in-del | -/T | 1.6489e-05 | 0.00287128 | | | GRCh38.p7 | 12:3812183 | AAAACCACAAAGATC[-/T]TTTGGGTTCCAGGTA | 57097 |
rs778727745 | snp | A/G | 1.76549e-05 | 0.00297105 | | | GRCh38.p7 | 12:3812464 | AGAGGACCAAGAAAA[A/G]CCAAGATTACTCCGA | 57097 |
rs778761342 | snp | A/G | 6.65668e-05 | 0.00576879 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3826198 | CTCTTTTTATTAAGC[A/G]CTGCTTTCCAGTGGT | 57097 |
rs778896131 | snp | C/T | 1.65091e-05 | 0.00287303 | synonymous-codon, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3821911 | TAGGTTTTGAATTCT[C/T]TGAATTCTTTTAATT | 57097 |
rs778902936 | snp | A/G | 1.73342e-05 | 0.00294394 | intron-variant | PARP11 | GRCh38.p7 | 12:3826283 | AAAGTACACTGTACT[A/G]TAAAGTGTCATGAAG | 57097 |
rs778958788 | in-del | -/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3829281 | ATAGAAATATAGTTA[-/T]TTTTCCAGATAATTA | 57097 |
rs778998788 | snp | C/T | | | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3871295 | ATGTTTCATACACAA[C/T]TATGCATTGCATAAA | 57097 |
rs779003482 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3849298 | ATCCAGCAACTCCAC[A/G]ACTGAGTATATACCT | 57097 |
rs779008506 | snp | C/T | | | intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3871971 | GGTGAGTGATAGAAA[C/T]TAGGATCCCTCTCCT | 57097 |
rs779011374 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3859296 | GTAGGCCGGTGCAGT[A/G]GCTCACGTCTGTAAT | 57097 |
rs779017032 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3857748 | CAGTGAAGCTAGACT[A/G]TAAGATTTTGTTATT | 57097 |
rs779031373 | snp | A/C | 1.69152e-05 | 0.00290814 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812129 | GAAGTGAAATCAATG[A/C]AAGTCTATCAAGTAC | 57097 |
rs779062200 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3823339 | AGAGCTTCTTTAGGT[C/T]AATACAAGCCAAGCT | 57097 |
rs779099834 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3842472 | ATTTAGGGGAGATAG[A/G]AGGAGATCAGGGATG | 57097 |
rs779100062 | snp | C/T | | | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3874381 | CCCGTGCCTCAGGCT[C/T]CTGAGTAGCTGGGAT | 57097 |
rs779133354 | snp | A/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3845584 | GGTAAATGTTTTGTC[A/T]TTTACTTAAGGATAC | 57097 |
rs779162532 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3842960 | TTGCACCAAATAGAA[A/G]TGTCTATTTTATTAT | 57097 |
rs779163560 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3821254 | AATATTTCAGAGAAC[C/T]GCTTATTTTAATTTT | 57097 |
rs779288619 | snp | C/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3851206 | TGACACAGAAGACAG[C/G]TGATTTCTGCATTTC | 57097 |
rs779411527 | snp | A/T | 1.64939e-05 | 0.0028717 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3822002 | TTGTGCAGAGGAATA[A/T]GCTGGAAAAATAAAT | 57097 |
rs779418904 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3864450 | AGTTGTGAAGTATTA[C/T]CTCCTCTTCCATTTT | 57097 |
rs779477253 | snp | C/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3860372 | GAGATCATCCGGGAT[C/G]CTTCCTTGGTTCAAC | 57097 |
rs779544445 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3843893 | TATGCAAATAACATA[A/G]TAGTAATTTCTCTTT | 57097 |
rs779571472 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3825440 | TTGACCAATGGAGAT[C/T]AATGTAGGTGGAAAC | 57097 |
rs779634116 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3831480 | TCAATTGCCTTGTCT[A/G]GGCCACAGTTGGCTC | 57097 |
rs779640514 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3817310 | GGGTTAAAGGGCATG[G/T]AGTATGGGCATAGGC | 57097 |
rs779687437 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3857241 | TGAAACAAACCTGTA[C/T]GTTGTGCACATGTAC | 57097 |
rs779713598 | in-del | -/TCTG | | | intron-variant | PARP11 | GRCh38.p7 | 12:3868496 | AGCCCAGCCTTCTTC[-/TCTG]AGCTCCAGACTTACC | 57097 |
rs779889864 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3842220 | TCTGTGGATAGCAGA[A/G]TGCAAAGACCAAAAG | 57097 |
rs779904809 | in-del | -/AG | | | intron-variant | PARP11 | GRCh38.p7 | 12:3834237 | ATGGAGACTTTGCTC[-/AG]GGGTAAAGACGAGCC | 57097 |
rs780117850 | in-del | -/A | 1.70586e-05 | 0.00292045 | intron-variant | PARP11 | GRCh38.p7 | 12:3813990 | TCCTCTAAAAAGAGG[-/A]AACTCTCTCCTGGGG | 57097 |
rs780118516 | snp | C/G | 1.64787e-05 | 0.00287038 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3822137 | GGTGGCATAGGGATG[C/G]CCTCGTTTTCACAGA | 57097 |
rs780129278 | snp | C/T | 3.29794e-05 | 0.00406061 | intron-variant | PARP11 | GRCh38.p7 | 12:3822023 | AAAAATAAATTTGCA[C/T]AGATTTACTGCAGTC | 57097 |
rs780160279 | snp | A/G | | | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3869976 | GTGTGGATATGCTGG[A/G]CAAAGGGATGATTCG | 57097 |
rs780194925 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | PARP11 | GRCh38.p7 | 12:3811579 | CAGCACTGCAAATAA[C/T]TGTCTTGTTTCTGAT | 57097 |
rs780215581 | snp | A/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3821328 | ATACCTTTAATAGCT[A/T]AAAGTTTTCTGTAAT | 57097 |
rs780221083 | snp | A/G | | | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3871185 | CCAGAAATGAGAGGG[A/G]AAGAATACTGATTAT | 57097 |
rs780229696 | snp | C/T | 1.67812e-05 | 0.0028966 | intron-variant | PARP11 | GRCh38.p7 | 12:3830028 | CATCTCCTGAAAAGC[C/T]AGAAGGAGGTGGAGG | 57097 |
rs780235921 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3833272 | TCCAGAATGACAGAA[C/T]AAGGAGCTCAGTGGA | 57097 |
rs780317526 | snp | C/G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3819735 | ACGTGGTCTAGCCCC[C/G/T]GCTAACTCTCTGACT | 57097 |
rs780320985 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3848716 | ACTACTAGAAGAAAA[C/T]ACTGGGGAAATAAGA | 57097 |
rs780325670 | snp | G/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3834425 | ATCACCTGAGGCCAG[G/T]AGTTTGAGACCAGCC | 57097 |
rs780384519 | in-del | -/GAAA | | | intron-variant | PARP11 | GRCh38.p7 | 12:3863622 | AAAATCAGCAAAGGG[-/GAAA]GAAACGCACATGGGG | 57097 |
rs780398397 | snp | A/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3835361 | TTACAGAATTTGTTC[A/T]GCTATATCACTGTTA | 57097 |
rs780504414 | snp | C/G | 3.2969e-05 | 0.00405998 | intron-variant | PARP11 | GRCh38.p7 | 12:3829882 | CTAAATTAAAGGAAA[C/G]GAGGTACCTGAAACA | 57097 |
rs780613912 | snp | G/T | 1.65228e-05 | 0.00287422 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812161 | CAGGATAGATTTGGT[G/T]GGCATCAAAAACCAC | 57097 |
rs780689893 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3841271 | ATAAGAATATTCTTC[A/G]ATTCTTCTTCAATCT | 57097 |
rs780692222 | snp | C/T | 1.6476e-05 | 0.00287014 | synonymous-codon, missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3829906 | TGAAACATGTGCCAC[C/T]TCCCACATTCTGCCA | 57097 |
rs780709397 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3836296 | TAGAGGCCAAAAGTT[A/G]GGAGACATCATTCTC | 57097 |
rs780730133 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3857984 | AAGTAGTTTAGCATG[A/G]AGGATGCCACAAATG | 57097 |
rs780793510 | snp | A/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3832261 | ATACAATTCCTTATC[A/T]AATTACACTATTTTT | 57097 |
rs780816412 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3864184 | GCTTTTTCTGCATGT[A/G]CTGGAATCACCACAT | 57097 |
rs780885271 | snp | G/T | 1.6477e-05 | 0.00287024 | intron-variant, missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3829015 | TGCTAACTGAACACT[G/T]ACTGTTGGTATCCGG | 57097 |
rs780952587 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3816314 | TTCTAGTTTTGAATC[A/C]CTCACAAGTGTGATA | 57097 |
rs780966690 | snp | A/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3837359 | CAACAGCTAAATTAC[A/T]AAGATCTCTAATCTC | 57097 |
rs780979785 | in-del | -/ACTG | | | intron-variant | PARP11 | GRCh38.p7 | 12:3843451 | CAGGTTTCTAGAGTT[-/ACTG]TGTGTGTATTTTTTT | 57097 |
rs780996986 | snp | A/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3849098 | GAGAAATGCAAACCA[A/T]AACCACAATGAGACA | 57097 |
rs781002036 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3860528 | GAAGGCAGAGCATCA[A/G]GCCAATCATTCATTT | 57097 |
rs781127034 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3859694 | AAATCCAGCTATATG[C/T]TGTCCACAGAAATAC | 57097 |
rs781131107 | snp | A/G | 3.29516e-05 | 0.00405891 | synonymous-codon, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3812273 | GTATTTGGAGTCTCC[A/G]TTTATGTAATCTCCA | 57097 |
rs781161198 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3811356 | ACTTTGAAGATGCAA[C/T]AAACACCTTGCACAG | 57097 |
rs781196980 | snp | A/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3833157 | TTAGCATGAGTATAG[A/T]ATCTTCAGGAAATCA | 57097 |
rs781208834 | snp | G/T | | | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3874276 | ATTTTATTTATTTAT[G/T]TAGGCAGAACCTCGC | 57097 |
rs781379698 | snp | A/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3845943 | AAAATTGCATTGTGT[A/T]ACAGAGCTGAAAATT | 57097 |
rs781393990 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3847351 | TGATATCAAAACCCA[A/G]TAAGGACACAACAAA | 57097 |
rs781466879 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3867466 | ACAATACCAAAAAGT[A/G]ATTCTATGTTTTCTA | 57097 |
rs781473239 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3826861 | GCCTCAGTCATACCA[A/G]TATTTACCAGGTCCA | 57097 |
rs781560196 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3854803 | GCATCACCCTGATAC[C/T]AAAGCCTGGCAGAGA | 57097 |
rs781560947 | snp | C/T | 1.69413e-05 | 0.00291039 | intron-variant | PARP11 | GRCh38.p7 | 12:3826155 | CTATTCTCTTTACCA[C/T]ACCTGAAAGCACTGA | 57097 |
rs781614028 | snp | C/T | 1.65026e-05 | 0.00287246 | missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3822155 | TCGTTTTCACAGATG[C/T]AACTTGAAACAGCAA | 57097 |
rs781704312 | snp | C/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3819519 | CAATCAAAAATGACT[C/G]CAGTCATTACCAAAT | 57097 |
rs781727990 | snp | A/G | | | intron-variant, upstream-variant-2KB | PARP11 | GRCh38.p7 | 12:3839551 | TTTGAAGCGATTATA[A/G]GAGGATCATTTGAAG | 57097 |
rs781743199 | snp | C/G | 1.6674e-05 | 0.00288734 | utr-variant-5-prime, missense, nc-transcript-variant | PARP11 | GRCh38.p7 | 12:3830018 | CTTTGTGAAACATCT[C/G]CTGAAAAGCCAGAAG | 57097 |
rs781769694 | snp | C/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3815812 | TTAAGCTTTACTTGA[C/T]ATAGTAATTTAAAAA | 57097 |
rs796206435 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3835936 | CATATAAATAACTAC[A/G]GTATCAGAAGCGGAG | 57097 |
rs796259514 | in-del | -/T | | | intron-variant | PARP11 | GRCh38.p7 | 12:3866664 | CTTTCAGATTATTTT[-/T]CACACAAAGCACAAA | 57097 |
rs796379316 | in-del | -/TC | | | intron-variant | PARP11 | GRCh38.p7 | 12:3831246 | TGCATATCTTTCAGA[-/TC]TCTCTCTCTCTCTCA | 57097 |
rs796413181 | in-del | -/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3817129 | CCGGAGGCGGAACTT[-/G]GCAGTGAGCTGAGAT | 57097 |
rs796475124 | snp | A/C | | | intron-variant, upstream-variant-2KB | PARP11, LOC105369609 | GRCh38.p7 | 12:3870567 | GACGCAGGAGGGAAA[A/C]TTCATAGTAGGAGCA | 57097 |
rs796650810 | in-del | CT/GCC | | | intron-variant | PARP11 | GRCh38.p7 | 12:3821735 | GAGAATGCTGAAGAG[CT/GCC]TGAGACCAGGTCAAA | 57097 |
rs796671533 | in-del | -/A | | | intron-variant | PARP11 | GRCh38.p7 | 12:3836331 | TACATAAAGTAAAAA[-/A]CAAACAAAAAAAAAG | 57097 |
rs796735031 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3817775 | ACTTTCATGCTCTGG[A/G]TTAAAATAAATTTGC | 57097 |
rs796744543 | snp | G/T | | | upstream-variant-2KB, intron-variant | PARP11, LOC105369609 | GRCh38.p7 | 12:3874986 | TAATCATTACATATT[G/T]AATATATTTGCCTTT | 57097 |
rs796860669 | snp | A/C | | | intron-variant | PARP11 | GRCh38.p7 | 12:3854746 | AACTATTCCAATCAA[A/C]AGAAAAAAAGGGAAT | 57097 |
rs796905137 | snp | A/G | | | intron-variant | PARP11 | GRCh38.p7 | 12:3817937 | GTAAATTCCACTGGC[A/G]ATTCTGACCTGCAAC | 57097 |