| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs749189190 | snp | A/G | 1.65608e-05 | 0.00287752 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65340539 | GAAAAGCGACACCGG[A/G]GTCCAGGTGAGGGTC | 5977 |
| rs749240628 | snp | A/G | 1.64795e-05 | 0.00287045 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65340454 | TCGCCTCTGTGCTGA[A/G]CGCAGCGTGCGCCTG | 5977 |
| rs749244157 | in-del | -/ATTA | 3.30393e-05 | 0.0040643 | intron-variant | DPF2 | GRCh38.p7 | 11:65348970 | CAGAACAATTACTTT[-/ATTA]GTTACTTGGAAAATA | 5977 |
| rs749275482 | snp | A/C/G | 4.94404e-05 | 0.00497173 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65345949 | AAAGGGTCCTGATGG[A/C/G]TTGGCCTTGCCCAAC | 5977 |
| rs749330822 | snp | A/G | 5.01232e-05 | 0.00500591 | intron-variant | DPF2 | GRCh38.p7 | 11:65340338 | ATAGCTCAGCACCCT[A/G]TGCCCCCCGCTCCAA | 5977 |
| rs749572868 | snp | C/T | 1.6522e-05 | 0.00287414 | missense, intron-variant | DPF2 | GRCh38.p7 | 11:65344022 | GTGCCCGTAAGAAGC[C/T]GGATGCTTCCATCCT | 5977 |
| rs749581620 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65342550 | ACAGTGAAGCACACT[C/T]AGTCTCTGCCAACAG | 5977 |
| rs749604204 | snp | G/T | 1.6476e-05 | 0.00287014 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65341439 | GGGGCTGATCTCTCA[G/T]GATGGCAGTAGTTTA | 5977 |
| rs749728645 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65338043 | TGACCTCAGGTGATC[C/T]GTCCACCTCAGTCTC | 5977 |
| rs750063210 | snp | C/T | 1.80781e-05 | 0.00300645 | intron-variant | DPF2 | GRCh38.p7 | 11:65346392 | CTCCTCAGCATGGCT[C/T]CTTCTGGGCTTTTAC | 5977 |
| rs750066231 | snp | A/G | 1.64765e-05 | 0.00287019 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65341426 | CCCTGAAGAAGGAGG[A/G]GCTGATCTCTCAGGA | 5977 |
| rs750124933 | snp | C/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65339826 | ATATCAGTATGTGAA[C/G]AGCTTCCTTCTTATG | 5977 |
| rs750164255 | in-del | -/TT | | | intron-variant | DPF2 | GRCh38.p7 | 11:65336247 | CTATAATCCCAACAC[-/TT]TGGGAGGTTGAGGCA | 5977 |
| rs750264412 | snp | A/C | | | intron-variant | DPF2 | GRCh38.p7 | 11:65350286 | GCTACAAGCTAAAAC[A/C]TATGGACCACATCCA | 5977 |
| rs750317661 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65348909 | GTACTGTCTCACCCC[A/G]TCCATGTCTGAGCCC | 5977 |
| rs750608775 | in-del | -/T | 6.73457e-05 | 0.00580244 | intron-variant | DPF2 | GRCh38.p7 | 11:65346197 | GCAGGAGCTCCTCTC[-/T]TTCCCCCCGCATTTC | 5977 |
| rs750677830 | snp | C/T | 1.65318e-05 | 0.002875 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65341063 | ACTTTCCTTCCCATC[C/T]ATTAAGCCAGGTAAG | 5977 |
| rs750866861 | snp | C/T | 1.64779e-05 | 0.00287031 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65345700 | GAACCGACCAGGCCT[C/T]AGTTACCACTATGCC | 5977 |
| rs750931920 | in-del | -/AA | | | intron-variant | DPF2 | GRCh38.p7 | 11:65337452 | GCAAGACTCTATCTC[-/AA]AAAAAAAAAAAAAAA | 5977 |
| rs750934031 | snp | C/T | | | intron-variant, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333935 | TGAGTGGTCGTTTCT[C/T]TCTCTCCTAGGGCGG | 5977 |
| rs750966513 | snp | A/G | 0.00064683 | 0.0179721 | intron-variant | DPF2 | GRCh38.p7 | 11:65344542 | TGTCTCAAGTGTATC[A/G]AGGCCTTCTTCTCAT | 5977 |
| rs750980561 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65343611 | GCATGCTTGAAAGGC[A/G]TTGGTGAGGAATGAG | 5977 |
| rs751055861 | snp | A/G | 3.48632e-05 | 0.00417497 | intron-variant | DPF2 | GRCh38.p7 | 11:65346372 | GACGTGTGTATCCCC[A/G]CCCCCTCCTCAGCAT | 5977 |
| rs751101849 | in-del | -/A | | | intron-variant | DPF2 | GRCh38.p7 | 11:65338332 | CAGTGTTTCCTTCCC[-/A]AGCCCTTTTACCCCC | 5977 |
| rs751170058 | in-del | -/A | | | intron-variant | DPF2 | GRCh38.p7 | 11:65336785 | GCAAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 5977 |
| rs751210033 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65338646 | CTCCAACGTGAGATT[C/T]GTGCCTACCTCAGAT | 5977 |
| rs751250323 | snp | A/G | 1.65083e-05 | 0.00287296 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65346250 | CCCCCACTACAGGGC[A/G]TCCATCTTGCCTCCA | 5977 |
| rs751262803 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65352130 | TGTTCTGCCTCCCCT[C/T]TGGTCTCCAGAGTTT | 5977 |
| rs751518020 | snp | A/C | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65341516 | ATCCCCGAGTTGATG[A/C]TGACAGCCTGGGCGA | 5977 |
| rs751527501 | snp | C/T | 3.29658e-05 | 0.00405978 | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65351770 | CTTGATGTGGCCACC[C/T]ACCTGCTCCCCGACA | 5977 |
| rs751720252 | snp | C/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65335004 | AAGTTGCTTCTCCCT[C/G]CTGCCTGAAGCCTTT | 5977 |
| rs751766863 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65348396 | ACCAGCCTGGGCAAC[A/G]TAAGGAGATCTTGTC | 5977 |
| rs751769514 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65348550 | TGCACCACTGCACTC[C/T]AGCCTGAGTGACAGC | 5977 |
| rs751814026 | snp | C/T | 3.30038e-05 | 0.00406212 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65340508 | AGTAGCCCAGAGCAA[C/T]TGTTACATCTGGATG | 5977 |
| rs751922422 | in-del | -/C | 3.29731e-05 | 0.00406023 | intron-variant | DPF2 | GRCh38.p7 | 11:65345835 | GAAGTGGTGGGCAAG[-/C]AGAAGTTGGCCTGGT | 5977 |
| rs751971354 | in-del | -/A | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65331893 | GGGAAACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 5977 |
| rs751972712 | snp | A/C/G | 5.08086e-05 | 0.00504005 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65333872 | TTCTCGGCCCGAGGC[A/C/G]GAGGAACAGGGAAGA | 5977 |
| rs751986292 | snp | G/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65343520 | TGGTGGGGAAAGCAT[G/T]TCAGGCTAAGGAAAT | 5977 |
| rs752072748 | snp | C/T | 1.65704e-05 | 0.00287836 | intron-variant | DPF2 | GRCh38.p7 | 11:65343972 | CAAAATAAGGGTGTC[C/T]CTTTGCTCTTCTTGG | 5977 |
| rs752174476 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65351864 | TCCTTCACAAATCCA[C/G]AGAACCTTGGGGTGG | 5977 |
| rs752185421 | snp | A/C | 1.6571e-05 | 0.0028784 | intron-variant | DPF2 | GRCh38.p7 | 11:65346100 | TTTGCCCAGTCCCCA[A/C]GGGGCTCTTGGCTTG | 5977 |
| rs752295485 | snp | C/T | 1.70516e-05 | 0.00291985 | utr-variant-5-prime, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333839 | GTCCCGGCGCCTGCG[C/T]GCTGCGGACTGTGGG | 5977 |
| rs752324542 | snp | A/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65351036 | GAGACTGTATGTGGC[A/T]CACACACCCTAAAAT | 5977 |
| rs752622090 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65338567 | ATTTTATTCTGTGTG[A/G]TGAAGACGTGGCTGC | 5977 |
| rs752651232 | snp | C/T | 5.10764e-05 | 0.00505328 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65346359 | CACCTCCGAGAATGA[C/T]GTGTGTATCCCCGCC | 5977 |
| rs752828892 | snp | C/T | 1.64988e-05 | 0.00287213 | intron-variant | DPF2 | GRCh38.p7 | 11:65345921 | CATCAAAACTCTTTC[C/T]CTCTGTAGCCAAAAA | 5977 |
| rs752844980 | snp | C/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65344327 | GCCACAGCAGGCAGG[C/G]TTGGCCTCTCAACAG | 5977 |
| rs752954228 | in-del | -/A | | | intron-variant | DPF2 | GRCh38.p7 | 11:65349800 | GACTCCATCTCAAAG[-/A]AAAAAAAAAAAAAGC | 5977 |
| rs752963300 | snp | C/T | 3.29592e-05 | 0.00405938 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65340403 | TGGGGAGCAGTACTA[C/T]AAAGATGCCATGGAG | 5977 |
| rs752984829 | snp | C/T | 3.29565e-05 | 0.00405921 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65345772 | CTCTCAACCACCCAC[C/T]CCTGTTTCCCAGAGG | 5977 |
| rs753001667 | snp | C/T | 5.32184e-05 | 0.00515814 | intron-variant | DPF2 | GRCh38.p7 | 11:65343740 | TAACCCTCCTGTCCA[C/T]TCAGCGGATCCTAGA | 5977 |
| rs753199658 | snp | A/G | 1.64784e-05 | 0.00287035 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65351758 | ACCAGAACTCCTCTT[A/G]ATGTGGCCACCCACC | 5977 |
| rs753280441 | multinucleotide-polymorphism | CA/TG | | | intron-variant | DPF2 | GRCh38.p7 | 11:65347107 | GCAACCTCTGCCTCC[CA/TG]GGTTCAAGTGATTCT | 5977 |
| rs753332286 | in-del | -/TGTTT | | | intron-variant | DPF2 | GRCh38.p7 | 11:65350082 | GAAGTCGCATGTTTA[-/TGTTT]TGTTTTGTTTTGTTT | 5977 |
| rs753499782 | snp | A/G | 1.65976e-05 | 0.00288072 | intron-variant | DPF2 | GRCh38.p7 | 11:65343717 | GATGCACATATTTCT[A/G]CCCATGCTAACCCTC | 5977 |
| rs753511183 | snp | A/C | 1.64768e-05 | 0.00287021 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65351744 | TTCCATCTACCAGAA[A/C]CAGAACTCCTCTTGA | 5977 |
| rs753577088 | snp | A/G | 1.702e-05 | 0.00291714 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65340966 | TTCTTCCTGCCACAG[A/G]ATTGGCCTCCGGACA | 5977 |
| rs753615132 | snp | A/G | 1.67239e-05 | 0.00289166 | intron-variant | DPF2 | GRCh38.p7 | 11:65346214 | TCCCCCCGCATTTCC[A/G]ACTGTCTGTCTCACT | 5977 |
| rs753750062 | snp | A/G/T | 1.69761e-05 | 0.00291337 | utr-variant-5-prime, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333862 | ACTGTGGGGCTTCTC[A/G/T]GCCCGAGGCAGAGGA | 5977 |
| rs753764312 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65350482 | CCGGGCTCAGGTAAT[C/T]TGGTAATCCTCCCAC | 5977 |
| rs753773852 | snp | A/G | 1.65548e-05 | 0.002877 | intron-variant | DPF2 | GRCh38.p7 | 11:65346088 | GAAGGCTGCTGCTTT[A/G]CCCAGTCCCCAAGGG | 5977 |
| rs753849958 | in-del | -/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65340124 | TTCTTTCACCTCTTT[-/G]GGGGTTAAACTTAAG | 5977 |
| rs753940788 | snp | A/C | 1.65337e-05 | 0.00287517 | missense, intron-variant | DPF2 | GRCh38.p7 | 11:65344033 | AAGCTGGATGCTTCC[A/C]TCCTGGAGGACCGGG | 5977 |
| rs753973411 | snp | A/G | 1.64895e-05 | 0.00287132 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65345933 | TTCTCTCTGTAGCCA[A/G]AAAGGGTCCTGATGG | 5977 |
| rs754034902 | in-del | -/A | | | intron-variant | DPF2 | GRCh38.p7 | 11:65337813 | GTTTTTTTTAATTTT[-/A]TTTTTTTTGAGACAG | 5977 |
| rs754400043 | snp | C/T | 1.64961e-05 | 0.00287189 | intron-variant | DPF2 | GRCh38.p7 | 11:65340382 | TTTCTATCTTCCCTG[C/T]AGCCTTGGGGAGCAG | 5977 |
| rs754480716 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | DPF2, TIGD3 | GRCh38.p7 | 11:65353136 | CCCCAATATGTAAAG[C/T]GAATATAAAATTGGT | 5977 |
| rs754543584 | in-del | -/A | | | intron-variant | DPF2 | GRCh38.p7 | 11:65343299 | GCGAAACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 5977 |
| rs754611988 | snp | G/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65350150 | GAATGGCTTTCCTAT[G/T]AAAGTTCTGTGGGAC | 5977 |
| rs754655142 | snp | C/T | 0.000137202 | 0.00828145 | intron-variant | DPF2 | GRCh38.p7 | 11:65343719 | TGCACATATTTCTAC[C/T]CATGCTAACCCTCCT | 5977 |
| rs754720218 | snp | A/G | 1.65334e-05 | 0.00287514 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65341064 | CTTTCCTTCCCATCT[A/G]TTAAGCCAGGTAAGG | 5977 |
| rs754795615 | snp | A/T | 1.69908e-05 | 0.00291463 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65340967 | TCTTCCTGCCACAGG[A/T]TTGGCCTCCGGACAG | 5977 |
| rs754909793 | in-del | -/C | 1.64817e-05 | 0.00287064 | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65351768 | CTCTTGATGTGGCCA[-/C]CCACCTGCTCCCCGA | 5977 |
| rs755004702 | snp | A/G | 1.65564e-05 | 0.00287714 | intron-variant | DPF2 | GRCh38.p7 | 11:65346092 | GCTGCTGCTTTGCCC[A/G]GTCCCCAAGGGGCTC | 5977 |
| rs755050905 | snp | A/G | 1.6486e-05 | 0.00287102 | missense, utr-variant-5-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65340389 | CTTCCCTGCAGCCTT[A/G]GGGAGCAGTACTACA | 5977 |
| rs755112635 | snp | C/G | 1.64779e-05 | 0.00287031 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65345761 | GACAAGGAAGACTCT[C/G]AACCACCCACTCCTG | 5977 |
| rs755310668 | snp | C/G | 1.66382e-05 | 0.00288424 | intron-variant | DPF2 | GRCh38.p7 | 11:65345621 | GATGGGGACATGGCA[C/G]TCTTGTATCCTAACA | 5977 |
| rs755350150 | snp | A/T | 1.64787e-05 | 0.00287038 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65341550 | TCCTGTGACCAACAG[A/T]CGAGCGCGAAAGGTA | 5977 |
| rs755354228 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65339864 | AGAATTTCATTGTAT[A/G]GATTTACCATAGTTT | 5977 |
| rs755354439 | in-del | -/A | | | intron-variant | DPF2 | GRCh38.p7 | 11:65342993 | ACGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 5977 |
| rs755370914 | snp | A/C | 3.2969e-05 | 0.00405998 | stop-gained, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65348888 | CTGCGATCGTGGCTA[A/C]CACATGTACTGTCTC | 5977 |
| rs755409357 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | DPF2, TIGD3 | GRCh38.p7 | 11:65353450 | AAGTTCTTGCAGGAG[C/G]AGGGTCTGTGTGGCT | 5977 |
| rs755424091 | snp | C/G | 1.86893e-05 | 0.00305685 | intron-variant | DPF2 | GRCh38.p7 | 11:65346400 | CATGGCTCCTTCTGG[C/G]CTTTTACTGCTGTTT | 5977 |
| rs755468024 | in-del | -/TT | | | intron-variant | DPF2 | GRCh38.p7 | 11:65350361 | TCTTTTCTCTTTTTC[-/TT]TTTCTTTCTTTCTTT | 5977 |
| rs755588550 | snp | G/T | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65341527 | GATGATGACAGCCTG[G/T]GCGAGTTTCCTGTGA | 5977 |
| rs755653992 | in-del | -/AGGGCTGTCATAACC | | | intron-variant | DPF2 | GRCh38.p7 | 11:65346125 | GGCTTGCTGGCCTCT[-/AGGGCTGTCATAACC]AGCCCACCTCGCTTT | 5977 |
| rs755784167 | snp | A/G | 1.64738e-05 | 0.00286995 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65348855 | CCTACTTCAGGACCA[A/G]TTGCTCTTCTGTGAT | 5977 |
| rs756098798 | snp | A/G | 3.29783e-05 | 0.00406055 | intron-variant | DPF2 | GRCh38.p7 | 11:65345840 | GGTGGGCAAGCAGAA[A/G]TTGGCCTGGTTATGA | 5977 |
| rs756132079 | snp | C/G | | | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65348924 | GTCCATGTCTGAGCC[C/G]CCTGAAGGTAAGTTG | 5977 |
| rs756194613 | in-del | -/T | 3.33381e-05 | 0.00408264 | intron-variant | DPF2 | GRCh38.p7 | 11:65346220 | GCATTTCCGACTGTC[-/T]TGTCTCACTCACTTC | 5977 |
| rs756244396 | snp | C/T | 0.000162509 | 0.00901267 | intron-variant | DPF2 | GRCh38.p7 | 11:65344638 | TAGCTCTCTCAACTT[C/T]TCAGACTTGTGGTTT | 5977 |
| rs756297367 | snp | C/T | 1.65179e-05 | 0.00287379 | missense, intron-variant | DPF2 | GRCh38.p7 | 11:65344012 | GGTGTGGGCAGTGCC[C/T]GTAAGAAGCTGGATG | 5977 |
| rs756322246 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65342428 | TCCAGCCTGGGTAAC[A/G]GAGGGAGACCCTGTC | 5977 |
| rs756369258 | in-del | -/TTTA | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333299 | TTTTTCTTTTTTTCC[-/TTTA]TTTATTTATTTATTT | 5977 |
| rs756458323 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65352143 | CTCTGGTCTCCAGAG[A/T]TTTCCTGTCCTCTAG | 5977 |
| rs756475845 | snp | C/T | 1.82727e-05 | 0.00302258 | intron-variant | DPF2 | GRCh38.p7 | 11:65346396 | TCAGCATGGCTCCTT[C/T]TGGGCTTTTACTGCT | 5977 |
| rs756617118 | snp | C/T | 8.98755e-05 | 0.00670296 | intron-variant, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333941 | GTCGTTTCTTTCTCT[C/T]CTAGGGCGGCAGGTT | 5977 |
| rs756710329 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65345532 | GCCGTCACTCAAGGC[C/T]TGTCCCAGAGTGGAG | 5977 |
| rs756775863 | snp | C/G | 1.648e-05 | 0.0028705 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65341406 | GCTTGCAGACACAGA[C/G]CAGACCCTGAAGAAG | 5977 |
| rs756830866 | snp | A/C/G | 3.32426e-05 | 0.00407681 | intron-variant | DPF2 | GRCh38.p7 | 11:65341083 | AGCCAGGTAAGGCAC[A/C/G]TACTTCCTGAGCAGA | 5977 |
| rs756854547 | snp | C/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65339785 | CTTGCTTTGCTTTTT[C/G]TCCCTAGTTAACTTG | 5977 |
| rs756909526 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | DPF2, TIGD3 | GRCh38.p7 | 11:65353148 | AAGCGAATATAAAAT[C/T]GGTTATTTTGTTTTG | 5977 |
| rs756909680 | snp | G/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65338662 | GTGCCTACCTCAGAT[G/T]ACAGTCATTACAGCT | 5977 |
| rs756980534 | snp | C/T | 4.94295e-05 | 0.00497115 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65345778 | ACCACCCACTCCTGT[C/T]TCCCAGAGGTCTGAG | 5977 |
| rs756982598 | snp | C/G | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65332868 | AAGTAGCTGGGATTA[C/G]AGGCATGAGGCATTG | 5977 |
| rs757092533 | in-del | -/C | 0.00279299 | 0.0372652 | intron-variant | DPF2 | GRCh38.p7 | 11:65346083 | CCGTGAAGGCTGCTG[-/C]CTTTGCCCAGTCCCC | 5977 |
| rs757103312 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65347459 | CCACCTCAGCCTCCC[A/G]GGTAGCTGGGACCAC | 5977 |
| rs757235832 | snp | C/T | 1.66474e-05 | 0.00288503 | intron-variant | DPF2 | GRCh38.p7 | 11:65346224 | TTTCCGACTGTCTGT[C/T]TCACTCACTTCCCCC | 5977 |
| rs757335854 | snp | C/T | 4.29581e-05 | 0.00463435 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65343795 | CGATGATGAAGACTA[C/T]GAAGAAGATACTCCC | 5977 |
| rs757388869 | snp | C/T | 4.94735e-05 | 0.00497336 | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65351781 | CACCCACCTGCTCCC[C/T]GACATATCTAAGGCT | 5977 |
| rs757571169 | snp | A/T | 1.8066e-05 | 0.00300544 | intron-variant | DPF2 | GRCh38.p7 | 11:65340951 | GCCTGACTTCTATCT[A/T]TCTTCCTGCCACAGG | 5977 |
| rs757688253 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | DPF2, TIGD3 | GRCh38.p7 | 11:65353366 | TCTCAGACATTTAAA[A/G]CAGGACCAGAAGTTT | 5977 |
| rs757811217 | in-del | -/TTTTC | | | intron-variant | DPF2 | GRCh38.p7 | 11:65350337 | TTGCAAGCTGTTTTG[-/TTTTC]TTTTCTTTTCTTTTC | 5977 |
| rs757826187 | snp | A/G | 3.35188e-05 | 0.00409369 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65340977 | ACAGGATTGGCCTCC[A/G]GACAGCTGTACTCCT | 5977 |
| rs757906468 | snp | G/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65338575 | CTGTGTGGTGAAGAC[G/T]TGGCTGCCTCCTAAA | 5977 |
| rs757960859 | snp | C/T | 1.65441e-05 | 0.00287607 | intron-variant | DPF2 | GRCh38.p7 | 11:65346241 | CACTCACTTCCCCCA[C/T]TACAGGGCATCCATC | 5977 |
| rs758009351 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65352029 | TTAAGTGCATTCACT[C/T]TGCTTGCCTTGGGCC | 5977 |
| rs758062427 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65351089 | AGAAAACTTTGCCAA[C/T]CGTATTGACCTTTGG | 5977 |
| rs758102145 | snp | A/C | | | intron-variant | DPF2 | GRCh38.p7 | 11:65341195 | GAATATGATGTGATT[A/C]TTTCCTTTAAGGACC | 5977 |
| rs758382756 | in-del | -/CT | | | intron-variant | DPF2 | GRCh38.p7 | 11:65348572 | AGTGACAGCAATACC[-/CT]GTCTCAAAAAAATAT | 5977 |
| rs758428310 | snp | A/G | 8.29139e-05 | 0.00643817 | intron-variant | DPF2 | GRCh38.p7 | 11:65341077 | CTATTAAGCCAGGTA[A/G]GGCACATACTTCCTG | 5977 |
| rs758475381 | snp | G/T | 1.64808e-05 | 0.00287057 | intron-variant | DPF2 | GRCh38.p7 | 11:65348944 | AAGGTAAGTTGCCCA[G/T]ATCTTTTACTCAGAA | 5977 |
| rs758588913 | snp | A/G | 1.64779e-05 | 0.00287031 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65340413 | TACTACAAAGATGCC[A/G]TGGAGCAGTGCCACA | 5977 |
| rs758840057 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65339997 | TCTAGGAAAGAGGGA[A/G]TAAGGAGGAACTTAG | 5977 |
| rs758885245 | snp | C/G/T | 3.29664e-05 | 0.00405984 | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65351768 | CTCTTGATGTGGCCA[C/G/T]CCACCTGCTCCCCGA | 5977 |
| rs759100794 | snp | A/G | 3.33467e-05 | 0.00408316 | intron-variant | DPF2 | GRCh38.p7 | 11:65343945 | AGAGTCTAACTCCTC[A/G]GGCCCAGCTACCAAA | 5977 |
| rs759255085 | snp | C/G | 1.66693e-05 | 0.00288693 | intron-variant | DPF2 | GRCh38.p7 | 11:65346220 | CGCATTTCCGACTGT[C/G]TGTCTCACTCACTTC | 5977 |
| rs759378527 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65339437 | TGATTCAGATTTCAA[A/G]TTGAGTCTTTTGAGA | 5977 |
| rs759394018 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65351650 | GTGGGGATTGTGTGG[A/G]ACCCATCCTGACCCC | 5977 |
| rs759638525 | snp | G/T | 0.000148489 | 0.00861525 | intron-variant | DPF2 | GRCh38.p7 | 11:65345915 | GGGTGTCATCAAAAC[G/T]CTTTCTCTCTGTAGC | 5977 |
| rs759872695 | snp | C/T | 0.000164758 | 0.0090748 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65351750 | CTACCAGAACCAGAA[C/T]TCCTCTTGATGTGGC | 5977 |
| rs759907005 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65334829 | GGGCTTGGTGCAAGG[A/G]TGGGAAAATTGAGTG | 5977 |
| rs760099769 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65348395 | GACCAGCCTGGGCAA[C/T]GTAAGGAGATCTTGT | 5977 |
| rs760153173 | snp | A/G | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65332368 | AATTTGTTAAGGAGC[A/G]ACAAGAGCAAAACTC | 5977 |
| rs760241195 | snp | C/T | 1.64757e-05 | 0.00287012 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65351734 | AAGAGAAAGCTTCCA[C/T]CTACCAGAACCAGAA | 5977 |
| rs760288872 | in-del | -/TAT | 4.27634e-05 | 0.00462384 | cds-indel, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65343792 | CTCGATGATGAAGAC[-/TAT]TATGAAGAAGATACT | 5977 |
| rs760321255 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65342063 | GTTCGAGACTGCAAT[A/G]AGTCATGATCATGCC | 5977 |
| rs760380335 | snp | A/G | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65332149 | AAAGCCTAGGCGGGC[A/G]GAACACATGAGGTCA | 5977 |
| rs760433341 | snp | A/G | 1.66891e-05 | 0.00288864 | intron-variant | DPF2 | GRCh38.p7 | 11:65340577 | GGGAGAAGGGGACTC[A/G]GGAGCATAAGGAGGA | 5977 |
| rs760519867 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65351529 | TTAGAGGTTTATCCC[A/G]GCTCAGGAAACCATG | 5977 |
| rs760559533 | in-del | -/AG | | | intron-variant | DPF2 | GRCh38.p7 | 11:65343426 | CCAGGGTGGCCAATC[-/AG]AGGCAGGAGAGGGCA | 5977 |
| rs760573239 | snp | A/G | 3.30732e-05 | 0.00406638 | intron-variant | DPF2 | GRCh38.p7 | 11:65343884 | GACAGGGTGGCCTAG[A/G]GAATTCCTTATTTTA | 5977 |
| rs760648644 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65350307 | ACCACATCCAGCCAC[A/G]GCCAGCTTAAATAGC | 5977 |
| rs760649788 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65348202 | AGGTGGGAGGATTGC[C/T]TGAACCCAGGAGTTT | 5977 |
| rs760665169 | snp | A/T | 1.69824e-05 | 0.00291392 | utr-variant-5-prime, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333860 | GGACTGTGGGGCTTC[A/T]CGGCCCGAGGCAGAG | 5977 |
| rs760692403 | snp | G/T | | | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | DPF2, TIGD3 | GRCh38.p7 | 11:65352908 | TGTCGCTTTGGAGTT[G/T]AGGTGTCTTTTTTTT | 5977 |
| rs760874409 | snp | C/T | 3.29511e-05 | 0.00405887 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65341475 | TCTGTTGCGCACTGA[C/T]CCCCTGGAGAAGCGA | 5977 |
| rs760880895 | snp | A/G | 1.64822e-05 | 0.00287068 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65340465 | CTGAGCGCAGCGTGC[A/G]CCTGCCTTTCTTGGA | 5977 |
| rs760914030 | snp | C/T | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65331953 | GCTTCTCTTTATGTA[C/T]ATTTCAATTAAAAGT | 5977 |
| rs760927784 | snp | A/G | 4.9534e-05 | 0.0049764 | intron-variant | DPF2 | GRCh38.p7 | 11:65341370 | TTTCAGCCCTTTTGA[A/G]CCTTGCTTTATCCTG | 5977 |
| rs761041594 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65338372 | TGCCTGCCTTATGTA[A/G]CTCACAAGAGCCCTG | 5977 |
| rs761135699 | snp | A/G | 3.30055e-05 | 0.00406222 | intron-variant | DPF2 | GRCh38.p7 | 11:65345902 | CAGGGACCCCCATGG[A/G]TGTCATCAAAACTCT | 5977 |
| rs761247048 | snp | C/T | 3.29522e-05 | 0.00405894 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65345742 | GGCTGAGGAGGAGGG[C/T]GAGGACAAGGAAGAC | 5977 |
| rs761289291 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65340812 | ATCTATTTTTCTTTT[C/T]CACAGACTATTCCAC | 5977 |
| rs761354272 | snp | C/G | 6.58989e-05 | 0.00573978 | intron-variant | DPF2 | GRCh38.p7 | 11:65348841 | CCTCTTCCCTCTTGC[C/G]TACTTCAGGACCAGT | 5977 |
| rs761500665 | snp | A/G | 1.64803e-05 | 0.00287052 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65340459 | TCTGTGCTGAGCGCA[A/G]CGTGCGCCTGCCTTT | 5977 |
| rs761516426 | snp | A/C | 3.3129e-05 | 0.00406982 | intron-variant | DPF2 | GRCh38.p7 | 11:65340363 | CTCCAACATACACGC[A/C]TGATTTCTATCTTCC | 5977 |
| rs761824499 | snp | A/G | 1.65441e-05 | 0.00287607 | intron-variant | DPF2 | GRCh38.p7 | 11:65341600 | AAGGGAGCTTTGATG[A/G]AAATCAGCCTCCTCT | 5977 |
| rs761879455 | snp | G/T | 1.64849e-05 | 0.00287092 | intron-variant | DPF2 | GRCh38.p7 | 11:65351659 | GTGTGGGACCCATCC[G/T]GACCCCATTTTGCCT | 5977 |
| rs761879535 | snp | A/G | 0.000131783 | 0.00811628 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65341519 | CCCGAGTTGATGATG[A/G]CAGCCTGGGCGAGTT | 5977 |
| rs761883390 | snp | C/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65336699 | GACGCTGAGGGAAGG[C/G]AATCACTTGAATCCA | 5977 |
| rs761898514 | snp | C/G | 1.65121e-05 | 0.00287329 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65341054 | GGATCCACGACTTTC[C/G]TTCCCATCTATTAAG | 5977 |
| rs761898626 | snp | C/T | 1.64849e-05 | 0.00287092 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65346302 | GGCAGTGAAGACATA[C/T]CGCTGGCAGTGCATC | 5977 |
| rs761921492 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65338132 | TTTAACGTTTTGTAG[A/G]GATGGGATCTCACTA | 5977 |
| rs762038511 | snp | A/G | 1.64819e-05 | 0.00287066 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65345685 | TGGAAAACGTTACAA[A/G]AACCGACCAGGCCTC | 5977 |
| rs762239338 | snp | A/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65345036 | TTACTTCTCAAGATG[A/T]CAAAATGCCTCATGG | 5977 |
| rs762247961 | snp | C/T | 3.4346e-05 | 0.00414389 | intron-variant | DPF2 | GRCh38.p7 | 11:65344121 | TGGACCCAGCTCCTG[C/T]TCTGGATATGAGAGG | 5977 |
| rs762382922 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65336957 | GCTGGGCATGGTGGC[A/G]TGCACCTGTAGTCCC | 5977 |
| rs762480201 | in-del | -/TA | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333038 | GTATATATATGTGTA[-/TA]TATATATATGTATAT | 5977 |
| rs762578638 | snp | C/T | 3.30142e-05 | 0.00406276 | intron-variant | DPF2 | GRCh38.p7 | 11:65345658 | TCTGCAATCTTCTTC[C/T]CACTCAGTTTGTGGA | 5977 |
| rs762631984 | snp | A/G | 1.67621e-05 | 0.00289495 | intron-variant | DPF2 | GRCh38.p7 | 11:65344089 | GTGCCTCACAAGTGG[A/G]TGGGTAGACCTTGCC | 5977 |
| rs762767384 | snp | C/T | 3.29506e-05 | 0.00405884 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65341498 | AGAAGCGAGGTGCCC[C/T]GGATCCCCGAGTTGA | 5977 |
| rs762855033 | snp | C/T | 1.64765e-05 | 0.00287019 | intron-variant | DPF2 | GRCh38.p7 | 11:65348826 | TTATTCAGTCCCCAT[C/T]CTCTTCCCTCTTGCC | 5977 |
| rs762876735 | snp | C/T | 3.90084e-05 | 0.00441618 | intron-variant | DPF2 | GRCh38.p7 | 11:65340939 | TACTGGGTTAGGGCC[C/T]GACTTCTATCTTTCT | 5977 |
| rs762892440 | snp | A/G | 1.64999e-05 | 0.00287222 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65340504 | CCGGAGTAGCCCAGA[A/G]CAATTGTTACATCTG | 5977 |
| rs762952357 | snp | C/T | 6.61376e-05 | 0.00575017 | intron-variant | DPF2 | GRCh38.p7 | 11:65346070 | TCAGGTACTGCTTCC[C/T]GTGAAGGCTGCTGCT | 5977 |
| rs762992208 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65334893 | TGACTGGATGACGAG[A/G]TAAAGGTTCGGTAAC | 5977 |
| rs763037630 | in-del | -/CT | | | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65352228 | GAGCTTTTCATGCCC[-/CT]GTGCCGCATAGCCTC | 5977 |
| rs763050135 | snp | A/G | 1.71469e-05 | 0.002928 | intron-variant | DPF2 | GRCh38.p7 | 11:65346362 | CTCCGAGAATGACGT[A/G]TGTATCCCCGCCCCC | 5977 |
| rs763087610 | snp | A/C | | | intron-variant | DPF2 | GRCh38.p7 | 11:65347481 | TGGGACCACAGATGC[A/C]CACCACCATGTCTGG | 5977 |
| rs763138623 | snp | A/G | 1.70055e-05 | 0.0029159 | utr-variant-5-prime, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333854 | CGCTGCGGACTGTGG[A/G]GCTTCTCGGCCCGAG | 5977 |
| rs763509929 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65336186 | TCTATCCCTTCCGAA[C/T]GTGATGTCAGAAATG | 5977 |
| rs763561629 | snp | C/G | 1.65042e-05 | 0.0028726 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65341032 | AGCGGCGAGCCCATC[C/G]CCCTGAGGATCCACG | 5977 |
| rs763652242 | snp | A/C | | | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | DPF2, TIGD3 | GRCh38.p7 | 11:65353093 | AAATACAGCTTTTTT[A/C]CCCCCAAATTAAAAT | 5977 |
| rs763709425 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65352116 | AGCTCACTTCTCTGT[A/G]TTCTGCCTCCCCTCT | 5977 |
| rs763960510 | snp | A/G | 1.65012e-05 | 0.00287234 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65340507 | GAGTAGCCCAGAGCA[A/G]TTGTTACATCTGGAT | 5977 |
| rs764046003 | snp | C/T | 3.30071e-05 | 0.00406232 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65341033 | GCGGCGAGCCCATCC[C/T]CCTGAGGATCCACGA | 5977 |
| rs764055932 | snp | C/T | 1.64773e-05 | 0.00287026 | intron-variant | DPF2 | GRCh38.p7 | 11:65348829 | TTCAGTCCCCATCCT[C/T]TTCCCTCTTGCCTAC | 5977 |
| rs764208872 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65334949 | ATCTGTCTTTGTCGT[A/G]GCCTGAGCCCCACTC | 5977 |
| rs764250607 | snp | C/T | 1.85844e-05 | 0.00304826 | intron-variant | DPF2 | GRCh38.p7 | 11:65340946 | TTAGGGCCTGACTTC[C/T]ATCTTTCTTCCTGCC | 5977 |
| rs764435076 | in-del | -/TCT | 3.30677e-05 | 0.00406605 | intron-variant | DPF2 | GRCh38.p7 | 11:65345650 | CACCTTTCTCTGCAA[-/TCT]TCTTCCCACTCAGTT | 5977 |
| rs764538172 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65336655 | TTAGCTGGGCATGGT[A/G]GCGTGTGTCTGTAAT | 5977 |
| rs764748473 | snp | C/T | 1.64925e-05 | 0.00287158 | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65351788 | CTGCTCCCCGACATA[C/T]CTAAGGCTGTTTCTC | 5977 |
| rs764803361 | snp | A/G | 1.66643e-05 | 0.0028865 | intron-variant | DPF2 | GRCh38.p7 | 11:65343946 | GAGTCTAACTCCTCA[A/G]GCCCAGCTACCAAAA | 5977 |
| rs764992910 | snp | C/T | 1.68046e-05 | 0.00289862 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65346350 | TATCTGCGGCACCTC[C/T]GAGAATGACGTGTGT | 5977 |
| rs764993031 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65339496 | ATTTTGTGAGAATGG[A/G]GAAGAACCCTAAGAT | 5977 |
| rs765121842 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | DPF2, TIGD3 | GRCh38.p7 | 11:65352924 | AGGTGTCTTTTTTTT[C/T]TCTTTCTTTAGTTCC | 5977 |
| rs765130489 | snp | A/G | 1.65669e-05 | 0.00287805 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65341073 | CCATCTATTAAGCCA[A/G]GTAAGGCACATACTT | 5977 |
| rs765171222 | snp | A/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65348997 | GAAAATACTGAGTTC[A/T]ATGTTCTTTATGTTA | 5977 |
| rs765229893 | snp | C/T | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65332384 | ACAAGAGCAAAACTC[C/T]GTCTCAAAATAAATA | 5977 |
| rs765356266 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65347339 | TCTTTATGTATTTAT[C/T]TATTTATTTTGAGAC | 5977 |
| rs765406677 | snp | G/T | 1.64985e-05 | 0.0028721 | intron-variant | DPF2 | GRCh38.p7 | 11:65345918 | TGTCATCAAAACTCT[G/T]TCTCTCTGTAGCCAA | 5977 |
| rs765573681 | snp | A/C/T | 6.77989e-05 | 0.00582193 | intron-variant | DPF2 | GRCh38.p7 | 11:65343720 | GCACATATTTCTACC[A/C/T]ATGCTAACCCTCCTG | 5977 |
| rs765632713 | snp | A/C | 4.94319e-05 | 0.00497127 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65351752 | ACCAGAACCAGAACT[A/C]CTCTTGATGTGGCCA | 5977 |
| rs765759689 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65334855 | GAGTGGTGTCTAGCT[A/G]TCCAGTCAGGGTTTT | 5977 |
| rs765853304 | in-del | -/TTTG | | | intron-variant | DPF2 | GRCh38.p7 | 11:65337781 | CTAGCTGATGGTTTT[-/TTTG]TTTGTTTGTTTGTTT | 5977 |
| rs765909866 | snp | C/T | 1.66715e-05 | 0.00288712 | intron-variant | DPF2 | GRCh38.p7 | 11:65343940 | CCAAAAGAGTCTAAC[C/T]CCTCAGGCCCAGCTA | 5977 |
| rs765911720 | snp | C/G | 1.64768e-05 | 0.00287021 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65351739 | AAAGCTTCCATCTAC[C/G]AGAACCAGAACTCCT | 5977 |
| rs765920926 | in-del | -/GT | 1.6588e-05 | 0.00287988 | intron-variant | DPF2 | GRCh38.p7 | 11:65343967 | GCTACCAAAATAAGG[-/GT]GTCTCTTTGCTCTTC | 5977 |
| rs765977052 | snp | A/C | | | intron-variant | DPF2 | GRCh38.p7 | 11:65342103 | CAGCCTGGGCAACAA[A/C]AAAAAAAAATTAAAA | 5977 |
| rs766063916 | in-del | -/ATATATATAGAGAGAGAGAGAGAGAG | | | intron-variant | DPF2 | GRCh38.p7 | 11:65337497 | TATATATATATATAT[-/ATATATATAGAGAGAGAGAGAGAGAG]AGAGAGAGAGAGAGA | 5977 |
| rs766070534 | snp | C/T | 3.29451e-05 | 0.00405851 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65348876 | CTTCTGTGATGACTG[C/T]GATCGTGGCTACCAC | 5977 |
| rs766136251 | snp | C/T | 1.74576e-05 | 0.00295441 | intron-variant | DPF2 | GRCh38.p7 | 11:65340958 | TTCTATCTTTCTTCC[C/T]GCCACAGGATTGGCC | 5977 |
| rs766152777 | snp | C/T | 8.3729e-05 | 0.00646973 | intron-variant | DPF2 | GRCh38.p7 | 11:65346213 | TTCCCCCCGCATTTC[C/T]GACTGTCTGTCTCAC | 5977 |
| rs766206157 | snp | C/T | 1.6599e-05 | 0.00288084 | intron-variant | DPF2 | GRCh38.p7 | 11:65346084 | CCGTGAAGGCTGCTG[C/T]TTTGCCCAGTCCCCA | 5977 |
| rs766291795 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | DPF2, TIGD3 | GRCh38.p7 | 11:65352938 | TTTCTTTCTTTAGTT[C/T]CTGTATTCTAAACAT | 5977 |
| rs766333849 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65337046 | GCACTCCAGCCCAGG[C/T]GACAGAGCGAGACTC | 5977 |
| rs766431202 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65340021 | AACTTAGGAGGGACT[A/G]TCATCTGCTTCTTAG | 5977 |
| rs766555584 | snp | A/G | 1.6476e-05 | 0.00287014 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65345739 | CTTGGCTGAGGAGGA[A/G]GGCGAGGACAAGGAA | 5977 |
| rs766753199 | snp | G/T | 6.59892e-05 | 0.00574371 | intron-variant | DPF2 | GRCh38.p7 | 11:65340381 | ATTTCTATCTTCCCT[G/T]CAGCCTTGGGGAGCA | 5977 |
| rs766779847 | snp | A/G | 1.64882e-05 | 0.00287121 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65340486 | CTTTCTTGGACTCAC[A/G]GACCGGAGTAGCCCA | 5977 |
| rs766812908 | snp | A/G | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65332102 | ATCAGCTGGCCAGGC[A/G]TGGTAGCTCATGCCT | 5977 |
| rs766917144 | in-del | -/A | | | intron-variant | DPF2 | GRCh38.p7 | 11:65339243 | GAGACCTTGTCTCTT[-/A]AAAAAAAAAAAAAAC | 5977 |
| rs766928686 | snp | C/T | 3.30087e-05 | 0.00406242 | intron-variant | DPF2 | GRCh38.p7 | 11:65345905 | GGACCCCCATGGGTG[C/T]CATCAAAACTCTTTC | 5977 |
| rs766937325 | snp | C/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65346986 | AAGGGTTTTACTCGG[C/G]AAGTGACATGGTTAT | 5977 |
| rs766982957 | snp | A/G/T | 9.88458e-05 | 0.00702952 | intron-variant | DPF2 | GRCh38.p7 | 11:65348843 | TCTTCCCTCTTGCCT[A/G/T]CTTCAGGACCAGTTG | 5977 |
| rs767043735 | snp | C/T | 1.64849e-05 | 0.00287092 | intron-variant | DPF2 | GRCh38.p7 | 11:65351662 | TGGGACCCATCCTGA[C/T]CCCATTTTGCCTCTC | 5977 |
| rs767055020 | in-del | -/CAAAAAAAAAAAA | | | intron-variant | DPF2 | GRCh38.p7 | 11:65343299 | AGCGAAACTCTGTCT[-/CAAAAAAAAAAAA]AAAAAAAAAAAGCTT | 5977 |
| rs767124481 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65339813 | TTGAAATTGTTTAAT[A/G]TCAGTATGTGAAGAG | 5977 |
| rs767127230 | snp | A/C/G | 8.23668e-05 | 0.00641696 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65341526 | TGATGATGACAGCCT[A/C/G]GGCGAGTTTCCTGTG | 5977 |
| rs767152414 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65335232 | AATTTAGAAATGACA[C/T]TGTTGATCTACCATT | 5977 |
| rs767154084 | snp | A/G | 3.57136e-05 | 0.00422558 | intron-variant | DPF2 | GRCh38.p7 | 11:65346386 | CGCCCCCTCCTCAGC[A/G]TGGCTCCTTCTGGGC | 5977 |
| rs767199700 | snp | C/T | 1.64969e-05 | 0.00287196 | intron-variant | DPF2 | GRCh38.p7 | 11:65345923 | TCAAAACTCTTTCTC[C/T]CTGTAGCCAAAAAGG | 5977 |
| rs767407036 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65352618 | CCAAAATCCCCTTTT[G/T]GTTCTTCCTGGACCT | 5977 |
| rs767480539 | snp | A/C | | | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65348851 | CTTGCCTACTTCAGG[A/C]CCAGTTGCTCTTCTG | 5977 |
| rs767499245 | snp | A/C | 1.65457e-05 | 0.00287621 | intron-variant | DPF2 | GRCh38.p7 | 11:65341602 | GGGAGCTTTGATGGA[A/C]ATCAGCCTCCTCTTC | 5977 |
| rs767603055 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65349561 | AGCACTTTGGGAGGC[C/T]GAGGTGGGCGGATCA | 5977 |
| rs767749748 | in-del | -/G | 1.65862e-05 | 0.00287973 | intron-variant | DPF2 | GRCh38.p7 | 11:65346110 | CCCCAAGGGGCTCTT[-/G]GCTTGCTGGCCTCTA | 5977 |
| rs767841883 | snp | C/T | 0.000161904 | 0.00899588 | intron-variant | DPF2 | GRCh38.p7 | 11:65344530 | TGCTGCTGCTCCTGT[C/T]TCAAGTGTATCAAGG | 5977 |
| rs767888485 | snp | A/G/T | 4.95784e-05 | 0.00497867 | intron-variant | DPF2 | GRCh38.p7 | 11:65340372 | ACACGCCTGATTTCT[A/G/T]TCTTCCCTGCAGCCT | 5977 |
| rs767976177 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65345269 | GGGTAAAAAAGTTTG[A/G]AGTCTTATCCACTTT | 5977 |
| rs768132085 | snp | A/G | 1.65034e-05 | 0.00287253 | intron-variant | DPF2 | GRCh38.p7 | 11:65345660 | TGCAATCTTCTTCCC[A/G]CTCAGTTTGTGGAAA | 5977 |
| rs768145152 | snp | C/T | 1.64795e-05 | 0.00287045 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65340455 | CGCCTCTGTGCTGAG[C/T]GCAGCGTGCGCCTGC | 5977 |
| rs768172009 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65343586 | GGAAGGGAGCAGGAG[C/T]AGGATTATAGCATGC | 5977 |
| rs768537493 | snp | A/G | 3.29924e-05 | 0.00406142 | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65351791 | CTCCCCGACATATCT[A/G]AGGCTGTTTCTCTCC | 5977 |
| rs768590373 | snp | C/G | 3.30186e-05 | 0.00406303 | intron-variant | DPF2 | GRCh38.p7 | 11:65351632 | CAGAGGAATTGCAAG[C/G]AGGTGGGGATTGTGT | 5977 |
| rs768625791 | snp | A/G | 1.65831e-05 | 0.00287945 | splice-donor-variant | DPF2 | GRCh38.p7 | 11:65340546 | GACACCGGGGTCCAG[A/G]TGAGGGTCCAGACTT | 5977 |
| rs768667874 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65350115 | TTTTTTAAACCATCA[A/G]ACAGATGATCTATGT | 5977 |
| rs768721684 | snp | A/G | 1.64822e-05 | 0.00287068 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65346296 | GATGGCGGCAGTGAA[A/G]ACATACCGCTGGCAG | 5977 |
| rs768779455 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65351275 | GTCAATATTAATAAA[C/T]AAGGAATGACCCAAT | 5977 |
| rs768788181 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65352323 | GAGTCAGGATGTTCT[C/T]GGTCACCCTCCTGGT | 5977 |
| rs768941561 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65338880 | TAATCTGTTTGCTGT[C/T]TCATCCCCAGGCTGT | 5977 |
| rs769112248 | in-del | -/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65344419 | TCAACGTCTGTTCTC[-/T]TTTTTCTTTCTGTCT | 5977 |
| rs769153526 | snp | C/T | 1.67694e-05 | 0.00289558 | intron-variant | DPF2 | GRCh38.p7 | 11:65341106 | TGAGCAGAGGCGTGG[C/T]CTGCTGCATGGTGAG | 5977 |
| rs769306006 | in-del | -/TCAAG | | | intron-variant | DPF2 | GRCh38.p7 | 11:65339031 | CAGGTCTTTTTACTC[-/TCAAG]TCAAGTCTGACTGTA | 5977 |
| rs769316501 | snp | C/T | 6.63427e-05 | 0.00575907 | synonymous-codon, intron-variant | DPF2 | GRCh38.p7 | 11:65344056 | GGACCGGGATAAGCC[C/T]TATGCCTGTGACAGT | 5977 |
| rs769629970 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65340304 | AGCCTTCTAGAGAAG[C/T]AGATGGCAGGGGAGA | 5977 |
| rs769671589 | snp | C/T | 1.66092e-05 | 0.00288172 | intron-variant | DPF2 | GRCh38.p7 | 11:65340356 | CCCCCCGCTCCAACA[C/T]ACACGCCTGATTTCT | 5977 |
| rs769800855 | snp | C/G | 1.70235e-05 | 0.00291744 | utr-variant-5-prime, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333848 | CCTGCGCGCTGCGGA[C/G]TGTGGGGCTTCTCGG | 5977 |
| rs769921860 | snp | C/G | 1.64784e-05 | 0.00287035 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65341549 | TTCCTGTGACCAACA[C/G]TCGAGCGCGAAAGGT | 5977 |
| rs770082049 | snp | C/T | 1.6483e-05 | 0.00287076 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65346275 | CCTCCAATTTACCCC[C/T]GTGATGATGGCGGCA | 5977 |
| rs770132557 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65337932 | GCCTCAGCCTCCCCC[A/G]TAGCTGGGATTATGG | 5977 |
| rs770186064 | snp | C/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65335937 | TCCTGCTTCAGCCTC[C/G]CGGGTAGCTGAGATT | 5977 |
| rs770311911 | snp | A/C | 1.65162e-05 | 0.00287365 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65341019 | CGCTGGCGGAAAAAG[A/C]GGCGAGCCCATCCCC | 5977 |
| rs770345669 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65344563 | TTCTTCTCATGACTT[C/T]TCTTTCTGTCTTTCA | 5977 |
| rs770651059 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65335564 | TGTAGAGATTGTGAG[C/T]ATCACCAGCCACTAA | 5977 |
| rs770763995 | snp | A/G | 4.9694e-05 | 0.00498443 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65341002 | ACTCCTACCCTGCCC[A/G]GCGCTGGCGGAAAAA | 5977 |
| rs770789972 | snp | C/T | 3.32392e-05 | 0.00407658 | intron-variant | DPF2 | GRCh38.p7 | 11:65345630 | ATGGCACTCTTGTAT[C/T]CTAACACCTTTCTCT | 5977 |
| rs770985409 | in-del | -/TATA | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333036 | ATGTATATATATGTG[-/TATA]TATATATATGTATAT | 5977 |
| rs770999788 | snp | C/T | 1.6498e-05 | 0.00287206 | intron-variant | DPF2 | GRCh38.p7 | 11:65348955 | CCCAGATCTTTTACT[C/T]AGAACAATTACTTTA | 5977 |
| rs771127121 | snp | A/G | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65341491 | CCCCTGGAGAAGCGA[A/G]GTGCCCCGGATCCCC | 5977 |
| rs771178775 | snp | G/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65340130 | CACCTCTTTGGGGGT[G/T]AAACTTAAGTCTGAT | 5977 |
| rs771267080 | snp | G/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65351016 | GAGTTAAAAAAAAAA[G/T]GCATGAGACTGTATG | 5977 |
| rs771319491 | snp | A/C | | | intron-variant | DPF2 | GRCh38.p7 | 11:65349379 | TTCTCCGATAACTTA[A/C]TGTAATAATGGTCCA | 5977 |
| rs771389355 | snp | C/T | 1.68937e-05 | 0.0029063 | intron-variant | DPF2 | GRCh38.p7 | 11:65346200 | AGGAGCTCCTCTCTT[C/T]CCCCCGCATTTCCGA | 5977 |
| rs771417853 | snp | A/G | 1.67933e-05 | 0.00289765 | intron-variant | DPF2 | GRCh38.p7 | 11:65340595 | AGCATAAGGAGGAAG[A/G]AGCCTCCTCATCTTA | 5977 |
| rs771502413 | snp | A/C | | | intron-variant | DPF2 | GRCh38.p7 | 11:65341850 | TGCAGTGGCTCATGC[A/C]TGTAATCCCAGCACT | 5977 |
| rs771572418 | snp | C/T | 6.59217e-05 | 0.00574078 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65340460 | CTGTGCTGAGCGCAG[C/T]GTGCGCCTGCCTTTC | 5977 |
| rs771613787 | snp | A/G | 3.33244e-05 | 0.0040818 | intron-variant | DPF2 | GRCh38.p7 | 11:65340572 | GACTTGGGAGAAGGG[A/G]ACTCAGGAGCATAAG | 5977 |
| rs771766737 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65335877 | GGAATGCAGTGGCAC[A/G]ATCTTGGCTCACTGC | 5977 |
| rs771824778 | in-del | -/AG | 5.00354e-05 | 0.00500152 | intron-variant | DPF2 | GRCh38.p7 | 11:65340577 | GGGAGAAGGGGACTC[-/AG]GAGCATAAGGAGGAA | 5977 |
| rs771839922 | snp | G/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65335372 | TAAAAAGGAAGATTC[G/T]CATTGTACTGGGGGA | 5977 |
| rs771965563 | snp | A/G | 1.65228e-05 | 0.00287422 | synonymous-codon, intron-variant | DPF2 | GRCh38.p7 | 11:65344023 | TGCCCGTAAGAAGCT[A/G]GATGCTTCCATCCTG | 5977 |
| rs772018820 | snp | A/G | 4.66038e-05 | 0.00482698 | intron-variant | DPF2 | GRCh38.p7 | 11:65343860 | GCCAGCGTGCTGCCT[A/G]CATCTTGGGACAGGG | 5977 |
| rs772164259 | snp | C/G | 3.30584e-05 | 0.00406548 | intron-variant | DPF2 | GRCh38.p7 | 11:65341361 | GCAGTCTGCTTTCAG[C/G]CCTTTTGAGCCTTGC | 5977 |
| rs772219515 | snp | A/G | 1.64882e-05 | 0.00287121 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65346304 | CAGTGAAGACATACC[A/G]CTGGCAGTGCATCGA | 5977 |
| rs772256871 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65346680 | TGCCATGAAAAAAAC[A/G]AAATCAGTACTGTGG | 5977 |
| rs772541919 | snp | C/T | 1.64806e-05 | 0.00287054 | intron-variant | DPF2 | GRCh38.p7 | 11:65351672 | CCTGACCCCATTTTG[C/T]CTCTCTGCAGGAAGT | 5977 |
| rs772659660 | in-del | -/ACTGG | | | intron-variant, utr-variant-5-prime | DPF2 | GRCh38.p7 | 11:65334548 | CATCAAAAACCTGCA[-/ACTGG]ACTGGACCGAAGCCG | 5977 |
| rs772681106 | snp | C/T | 3.33439e-05 | 0.00408299 | intron-variant | DPF2 | GRCh38.p7 | 11:65340574 | CTTGGGAGAAGGGGA[C/T]TCAGGAGCATAAGGA | 5977 |
| rs772733412 | snp | A/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65342733 | AAAACTTCCCATGGG[A/T]CGGGCACGGTAGCTC | 5977 |
| rs772792437 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65335488 | GTGCTTTCAAGTTGT[A/G]TCATAAGTGAGGGGT | 5977 |
| rs772946750 | snp | C/T | 1.64819e-05 | 0.00287066 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65340464 | GCTGAGCGCAGCGTG[C/T]GCCTGCCTTTCTTGG | 5977 |
| rs772947677 | in-del | -/G | 1.67649e-05 | 0.0028952 | intron-variant | DPF2 | GRCh38.p7 | 11:65340593 | GAGCATAAGGAGGAA[-/G]GAAGCCTCCTCATCT | 5977 |
| rs773005168 | snp | A/G | 3.29506e-05 | 0.00405884 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65345997 | CCTGGGGGACTCAAA[A/G]ATTAACAAGAAGACG | 5977 |
| rs773178678 | snp | C/T | 0.000118897 | 0.00770937 | utr-variant-5-prime, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333859 | CGGACTGTGGGGCTT[C/T]TCGGCCCGAGGCAGA | 5977 |
| rs773189453 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65341292 | TCCTGGGCGTGCAGA[A/G]AACAAAAGATAGTGA | 5977 |
| rs773263234 | snp | G/T | 4.39493e-05 | 0.00468751 | intron-variant | DPF2 | GRCh38.p7 | 11:65343878 | TCTTGGGACAGGGTG[G/T]CCTAGGGAATTCCTT | 5977 |
| rs773318082 | snp | C/T | 1.66263e-05 | 0.00288321 | intron-variant | DPF2 | GRCh38.p7 | 11:65341612 | ATGGAAATCAGCCTC[C/T]TCTTCACTGGGGGCC | 5977 |
| rs773339078 | snp | C/T | 1.6519e-05 | 0.00287388 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65346323 | GCAGTGCATCGAGTG[C/T]AAATGTTGCAATATC | 5977 |
| rs773401815 | snp | G/T | 1.65127e-05 | 0.00287334 | intron-variant | DPF2 | GRCh38.p7 | 11:65341367 | TGCTTTCAGCCCTTT[G/T]GAGCCTTGCTTTATC | 5977 |
| rs773462647 | snp | C/T | 5.74652e-05 | 0.00535997 | intron-variant | DPF2 | GRCh38.p7 | 11:65346407 | CCTTCTGGGCTTTTA[C/T]TGCTGTTTGCACAGT | 5977 |
| rs773468597 | snp | A/C | | | intron-variant | DPF2 | GRCh38.p7 | 11:65338311 | ATGAGATTCTCCCCC[A/C]ACACTTCAGTGTTTC | 5977 |
| rs773551253 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65352722 | CATGGGGAAGCCACA[C/T]AGACATCCCTTTCTT | 5977 |
| rs773586662 | snp | C/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65345273 | AAAAAAGTTTGGAGT[C/G]TTATCCACTTTTCCC | 5977 |
| rs773638413 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65346831 | ATCCCAGGAAAGGAG[C/T]AGCCAGCGCCAAGGC | 5977 |
| rs773774048 | snp | A/G | 1.65045e-05 | 0.00287263 | intron-variant | DPF2 | GRCh38.p7 | 11:65345901 | TCAGGGACCCCCATG[A/G]GTGTCATCAAAACTC | 5977 |
| rs773812293 | snp | A/C | | | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65340513 | CCCAGAGCAATTGTT[A/C]CATCTGGATGGAAAA | 5977 |
| rs773856468 | snp | C/T | 1.65034e-05 | 0.00287253 | intron-variant | DPF2 | GRCh38.p7 | 11:65345899 | GCTCAGGGACCCCCA[C/T]GGGTGTCATCAAAAC | 5977 |
| rs773887859 | snp | A/G | 1.648e-05 | 0.0028705 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65340458 | CTCTGTGCTGAGCGC[A/G]GCGTGCGCCTGCCTT | 5977 |
| rs773939317 | snp | C/T | 1.65726e-05 | 0.00287855 | intron-variant | DPF2 | GRCh38.p7 | 11:65340362 | GCTCCAACATACACG[C/T]CTGATTTCTATCTTC | 5977 |
| rs774054134 | snp | A/G | 1.64901e-05 | 0.00287137 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65345671 | TCCCACTCAGTTTGT[A/G]GAAAACGTTACAAGA | 5977 |
| rs774123172 | snp | C/T | | | intron-variant, utr-variant-5-prime | DPF2 | GRCh38.p7 | 11:65334574 | AGCCGTTCAGGACAG[C/T]TTAGCCTAAAGGGGC | 5977 |
| rs774185071 | in-del | -/TCTC | 1.77819e-05 | 0.00298172 | intron-variant, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333936 | GAGTGGTCGTTTCTT[-/TCTC]TCCTAGGGCGGCAGG | 5977 |
| rs774306178 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65351347 | AAACTACACAAGTCT[C/T]AAAACTGAGGTGCTT | 5977 |
| rs774350717 | snp | A/G | 1.65436e-05 | 0.00287602 | intron-variant | DPF2 | GRCh38.p7 | 11:65341599 | TAAGGGAGCTTTGAT[A/G]GAAATCAGCCTCCTC | 5977 |
| rs774405814 | snp | C/T | 3.29864e-05 | 0.00406105 | intron-variant | DPF2 | GRCh38.p7 | 11:65351652 | GGGGATTGTGTGGGA[C/T]CCATCCTGACCCCAT | 5977 |
| rs774458671 | snp | C/T | 1.64754e-05 | 0.00287009 | intron-variant | DPF2 | GRCh38.p7 | 11:65348834 | TCCCCATCCTCTTCC[C/T]TCTTGCCTACTTCAG | 5977 |
| rs774473883 | snp | A/C | 1.64833e-05 | 0.00287078 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65346299 | GGCGGCAGTGAAGAC[A/C]TACCGCTGGCAGTGC | 5977 |
| rs774494402 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65336584 | ATCACAAGGTCAGGA[A/G]ATTGAGACCATCCTG | 5977 |
| rs774528841 | snp | A/C/G | 3.35133e-05 | 0.00409338 | intron-variant | DPF2 | GRCh38.p7 | 11:65346208 | CTCTCTTCCCCCCGC[A/C/G]TTTCCGACTGTCTGT | 5977 |
| rs774551990 | snp | C/T | 1.65102e-05 | 0.00287312 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65341052 | GAGGATCCACGACTT[C/T]CCTTCCCATCTATTA | 5977 |
| rs774621226 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65350147 | ACAGAATGGCTTTCC[C/T]ATTAAAGTTCTGTGG | 5977 |
| rs774728257 | snp | A/G | 1.68289e-05 | 0.00290072 | intron-variant | DPF2 | GRCh38.p7 | 11:65341114 | GGCGTGGCCTGCTGC[A/G]TGGTGAGAGCCTGCT | 5977 |
| rs774816661 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65344955 | TGTTCCCCACTGCCC[C/T]ACCACCTCCTCCTGC | 5977 |
| rs774904053 | snp | A/C | 1.72044e-05 | 0.0029329 | missense, upstream-variant-2KB, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65333915 | TGGAGAATGTAGTGA[A/C]GCTGTGAGTGGTCGT | 5977 |
| rs775204450 | snp | C/T | 1.64784e-05 | 0.00287035 | intron-variant | DPF2 | GRCh38.p7 | 11:65348821 | ATCAGTTATTCAGTC[C/T]CCATCCTCTTCCCTC | 5977 |
| rs775243539 | snp | A/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65342594 | ACATGTAAAAATAAC[A/T]GCTATAAATATGCCA | 5977 |
| rs775488327 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65339601 | GACATCTTCCATAAA[C/T]GTAAAATTAATTAGT | 5977 |
| rs775512517 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65349655 | AAAAAAATTAGCCGG[C/T]TGTGGTGGCGGGCGC | 5977 |
| rs775541722 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | DPF2, TIGD3 | GRCh38.p7 | 11:65352971 | GTAAAAATAAATGTT[C/T]TTACACAGAGCCCTC | 5977 |
| rs775563619 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65348498 | AGGTAGGAGGATCAC[C/T]TGGGCCCAGGAGGTC | 5977 |
| rs775695232 | snp | C/T | 4.9534e-05 | 0.0049764 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65346054 | TTCTGACTGTGGCCG[C/T]TCAGGTACTGCTTCC | 5977 |
| rs775719594 | snp | A/G | 1.70139e-05 | 0.00291662 | utr-variant-5-prime, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333850 | TGCGCGCTGCGGACT[A/G]TGGGGCTTCTCGGCC | 5977 |
| rs775863845 | snp | A/G/T | 4.68922e-05 | 0.00484189 | intron-variant | DPF2 | GRCh38.p7 | 11:65343856 | AGGGGCCAGCGTGCT[A/G/T]CCTGCATCTTGGGAC | 5977 |
| rs775873302 | in-del | -/CAAGTGGGTGGGTAGAC | 1.67066e-05 | 0.00289016 | intron-variant | DPF2 | GRCh38.p7 | 11:65344082 | ACAGTGAGTGCCTCA[-/CAAGTGGGTGGGTAGAC]CTTGCCTTGGACCCA | 5977 |
| rs776097797 | snp | G/T | 6.18729e-05 | 0.00556171 | intron-variant | DPF2 | GRCh38.p7 | 11:65340929 | TACTTTCTAATACTG[G/T]GTTAGGGCCTGACTT | 5977 |
| rs776214008 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65344697 | TCCTCCTGCCTTTCT[C/T]ATTTCCTGGGATGCT | 5977 |
| rs776301156 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65352802 | CAAGTTTTCTGCTTA[A/G]TGGCACTGACATTAA | 5977 |
| rs776394628 | snp | G/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65336348 | ACTATAAAAATTAGT[G/T]AGGTGTGGTGGCGCA | 5977 |
| rs776435445 | snp | C/T | 1.65553e-05 | 0.00287705 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65341004 | TCCTACCCTGCCCGG[C/T]GCTGGCGGAAAAAGC | 5977 |
| rs776486213 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65338653 | GTGAGATTCGTGCCT[A/G]CCTCAGATTACAGTC | 5977 |
| rs776573880 | snp | C/T | 1.70307e-05 | 0.00291806 | missense, upstream-variant-2KB, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65333900 | AGATGGCGGCTGTGG[C/T]GGAGAATGTAGTGAA | 5977 |
| rs776714120 | snp | C/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65343482 | CCTTTTGGAAGCATG[C/G]TATTTGATTTGGCCA | 5977 |
| rs776722476 | snp | A/G | 4.94238e-05 | 0.00497086 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65341494 | CTGGAGAAGCGAGGT[A/G]CCCCGGATCCCCGAG | 5977 |
| rs776814812 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65335902 | CACTGCAACCTCCGC[C/T]TCCCGGGTTCCAGCA | 5977 |
| rs776862880 | snp | A/T | 1.65111e-05 | 0.0028732 | intron-variant | DPF2 | GRCh38.p7 | 11:65341580 | ACAGGATTATCCCTG[A/T]GGCTAAGGGAGCTTT | 5977 |
| rs776916116 | snp | A/T | 1.65091e-05 | 0.00287303 | intron-variant | DPF2 | GRCh38.p7 | 11:65348963 | TTTTACTCAGAACAA[A/T]TACTTTATTAGTTAC | 5977 |
| rs776975064 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65340249 | CATGAGGCAGAAGTG[A/G]AGGCAAATAGAACGG | 5977 |
| rs777106743 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65348308 | ATAGTCACTGGGCAC[A/G]GCGTCTCACACCTGT | 5977 |
| rs777134002 | snp | A/G | 1.65883e-05 | 0.00287991 | intron-variant | DPF2 | GRCh38.p7 | 11:65341078 | TATTAAGCCAGGTAA[A/G]GCACATACTTCCTGA | 5977 |
| rs777175590 | snp | A/G | 3.3618e-05 | 0.00409974 | intron-variant | DPF2 | GRCh38.p7 | 11:65340597 | CATAAGGAGGAAGAA[A/G]CCTCCTCATCTTAGG | 5977 |
| rs777383722 | snp | C/T | 1.66338e-05 | 0.00288386 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65340988 | CTCCGGACAGCTGTA[C/T]TCCTACCCTGCCCGG | 5977 |
| rs777452955 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65337866 | CTGGAGTGCAATGGC[A/G]CAATCTCGGCTCACC | 5977 |
| rs777497338 | snp | A/G | 1.65244e-05 | 0.00287436 | missense, intron-variant | DPF2 | GRCh38.p7 | 11:65344025 | CCCGTAAGAAGCTGG[A/G]TGCTTCCATCCTGGA | 5977 |
| rs777520682 | snp | C/T | 1.65844e-05 | 0.00287957 | intron-variant | DPF2 | GRCh38.p7 | 11:65346107 | AGTCCCCAAGGGGCT[C/T]TTGGCTTGCTGGCCT | 5977 |
| rs777536145 | snp | C/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65338346 | CCAGCCCTTTTACCC[C/G]CAAGACTGTTTGCCT | 5977 |
| rs777783511 | snp | G/T | 1.64852e-05 | 0.00287094 | intron-variant | DPF2 | GRCh38.p7 | 11:65348948 | TAAGTTGCCCAGATC[G/T]TTTACTCAGAACAAT | 5977 |
| rs777959716 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65347983 | GATGACTTTGGGTGC[C/T]GTGTGGAGGGTAGAC | 5977 |
| rs777985616 | in-del | -/CA | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65332322 | GAGCTGAGATAGTGC[-/CA]CACTGCACTCTAGCC | 5977 |
| rs778013466 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65346458 | TTTTAAAAAGGGAGC[A/G]GGATCCCTCCCACAT | 5977 |
| rs778479588 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | DPF2, TIGD3 | GRCh38.p7 | 11:65353182 | CATAAATTCAAGTTT[A/G]TAACAATTCTTTGTT | 5977 |
| rs778555341 | snp | A/G | 6.59076e-05 | 0.00574016 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65345963 | GATTGGCCTTGCCCA[A/G]CAACTACTGTGACTT | 5977 |
| rs778588185 | snp | A/G | 5.11112e-05 | 0.005055 | utr-variant-5-prime, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333836 | GCGGTCCCGGCGCCT[A/G]CGCGCTGCGGACTGT | 5977 |
| rs778588357 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65350326 | AGCTTAAATAGCTTG[C/T]AAGCTGTTTTGTTTT | 5977 |
| rs778602589 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65349172 | AAGCAGATGCTGAGC[C/T]GAGATCAGGCACCCA | 5977 |
| rs778618525 | in-del | -/TCTC | 1.65068e-05 | 0.00287283 | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65351800 | ATATCTAAGGCTGTT[-/TCTC]TCCTCCACTTCATAT | 5977 |
| rs778732858 | snp | C/T | 1.65649e-05 | 0.00287788 | | | GRCh38.p7 | 11:65346096 | CTGCTTTGCCCAGTC[C/T]CCAAGGGGCTCTTGG | 5977 |
| rs778752988 | snp | A/C/T | 5.03532e-05 | 0.00501742 | | | GRCh38.p7 | 11:65340976 | CACAGGATTGGCCTC[A/C/T]GGACAGCTGTACTCC | 5977 |
| rs778840846 | snp | A/C | 1.66056e-05 | 0.00288141 | intron-variant | DPF2 | GRCh38.p7 | 11:65340554 | GGTCCAGGTGAGGGT[A/C]CAGACTTGGGAGAAG | 5977 |
| rs778915788 | snp | C/T | 1.65018e-05 | 0.00287239 | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65351796 | CGACATATCTAAGGC[C/T]GTTTCTCTCCTCCAC | 5977 |
| rs778963899 | snp | A/G | 4.94287e-05 | 0.00497111 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65345763 | CAAGGAAGACTCTCA[A/G]CCACCCACTCCTGTT | 5977 |
| rs779009395 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65352544 | CCAGGCCAGCAGCTC[A/G]GGGGCCACAAGGAGA | 5977 |
| rs779191866 | snp | A/G | 1.64806e-05 | 0.00287054 | missense, utr-variant-5-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65340399 | GCCTTGGGGAGCAGT[A/G]CTACAAAGATGCCAT | 5977 |
| rs779210808 | snp | C/G | 1.66399e-05 | 0.00288438 | intron-variant | DPF2 | GRCh38.p7 | 11:65345623 | TGGGGACATGGCACT[C/G]TTGTATCCTAACACC | 5977 |
| rs779211493 | snp | A/C | | | intron-variant | DPF2 | GRCh38.p7 | 11:65339935 | TTCCCTCTGGAGCAG[A/C]CCTTGGGGCAAGGAT | 5977 |
| rs779290988 | snp | A/G | 1.64795e-05 | 0.00287045 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65341552 | CTGTGACCAACAGTC[A/G]AGCGCGAAAGGTACA | 5977 |
| rs779323312 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65336656 | TAGCTGGGCATGGTG[A/G]CGTGTGTCTGTAATC | 5977 |
| rs779401217 | snp | A/C/G | 9.39742e-05 | 0.00685415 | intron-variant | DPF2 | GRCh38.p7 | 11:65346401 | ATGGCTCCTTCTGGG[A/C/G]TTTTACTGCTGTTTG | 5977 |
| rs779430281 | snp | C/T | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65341453 | AGGATGGCAGTAGTT[C/T]AGAGGCTCTGTTGCG | 5977 |
| rs779590454 | snp | C/T | 0.000148279 | 0.00860914 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65341429 | TGAAGAAGGAGGGGC[C/T]GATCTCTCAGGATGG | 5977 |
| rs779661518 | snp | C/T | | | intron-variant, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65334020 | AGAGAGGGACATCCC[C/T]GGGAAAGCCATGTTG | 5977 |
| rs779712701 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65347812 | AGGCGCCCGCCACCA[C/T]GCCTGGCTAATTTTT | 5977 |
| rs779721071 | snp | A/G | 1.64776e-05 | 0.00287028 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65341546 | AGTTTCCTGTGACCA[A/G]CAGTCGAGCGCGAAA | 5977 |
| rs779885840 | snp | C/G | 4.96553e-05 | 0.00498249 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65340535 | GATGGAAAAGCGACA[C/G]CGGGGTCCAGGTGAG | 5977 |
| rs779922590 | snp | A/G | 3.2969e-05 | 0.00405998 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65345938 | TCTGTAGCCAAAAAG[A/G]GTCCTGATGGATTGG | 5977 |
| rs780053425 | in-del | -/CTCA | 1.66513e-05 | 0.00288537 | intron-variant | DPF2 | GRCh38.p7 | 11:65346224 | TTTCCGACTGTCTGT[-/CTCA]CTCACTTCCCCCACT | 5977 |
| rs780107295 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65335520 | GCCCATTTAAACAGA[A/G]CGTGACATCTTGTTT | 5977 |
| rs780109088 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65342492 | GTGCTTTACTCTTTT[A/G]TCACAAAAGTTTGTG | 5977 |
| rs780157572 | snp | A/C | 1.67312e-05 | 0.00289229 | intron-variant | DPF2 | GRCh38.p7 | 11:65340334 | AGGAATAGCTCAGCA[A/C]CCTATGCCCCCCGCT | 5977 |
| rs780245336 | snp | A/G | | | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65343813 | AGAAGATACTCCCAA[A/G]CGTCGGGGAAAGGGG | 5977 |
| rs780324003 | snp | G/T | 0.000324939 | 0.0127422 | intron-variant | DPF2 | GRCh38.p7 | 11:65344659 | CTTGTGGTTTTCCTT[G/T]CCCTTTTTCCCTCTT | 5977 |
| rs780339799 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65338688 | CAGCTCATTGAATCA[C/T]GCCAGGCTATATTTG | 5977 |
| rs780379193 | snp | G/T | 1.65195e-05 | 0.00287393 | missense, intron-variant | DPF2 | GRCh38.p7 | 11:65344013 | GTGTGGGCAGTGCCC[G/T]TAAGAAGCTGGATGC | 5977 |
| rs780466472 | snp | C/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65337963 | TCATGTACCACCACG[C/G]CCGGCTAATTTTGTA | 5977 |
| rs780522954 | snp | A/T | 4.98824e-05 | 0.00499387 | intron-variant | DPF2 | GRCh38.p7 | 11:65346227 | CCGACTGTCTGTCTC[A/T]CTCACTTCCCCCACT | 5977 |
| rs780896267 | snp | A/G | 1.64776e-05 | 0.00287028 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65341419 | GACCAGACCCTGAAG[A/G]AGGAGGGGCTGATCT | 5977 |
| rs780942025 | snp | A/G | 1.66062e-05 | 0.00288146 | intron-variant | DPF2 | GRCh38.p7 | 11:65345633 | GCACTCTTGTATCCT[A/G]ACACCTTTCTCTGCA | 5977 |
| rs781004664 | snp | C/T | 1.64923e-05 | 0.00287156 | synonymous-codon, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65346260 | AGGGCATCCATCTTG[C/T]CTCCAATTTACCCCC | 5977 |
| rs781020164 | snp | A/G | 3.29544e-05 | 0.00405908 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65340426 | CCATGGAGCAGTGCC[A/G]CAATTACAATGCTCG | 5977 |
| rs781069428 | in-del | -/A/AA | | | intron-variant | DPF2 | GRCh38.p7 | 11:65348613 | TTGGGCTTTAGGGAA[-/A/AA]AAAAAAAAAAAAAAA | 5977 |
| rs781079354 | snp | G/T | 1.64817e-05 | 0.00287064 | intron-variant | DPF2 | GRCh38.p7 | 11:65345813 | AGAAATGTAAGCTGA[G/T]GTGTCAGAAGTGGTG | 5977 |
| rs781113587 | snp | A/C/G | 0.000102135 | 0.00714551 | utr-variant-5-prime, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333847 | GCCTGCGCGCTGCGG[A/C/G]CTGTGGGGCTTCTCG | 5977 |
| rs781153161 | snp | A/G | | | intron-variant | DPF2 | GRCh38.p7 | 11:65347614 | GCTGGGATTACAGGC[A/G]TGAACCCACCATGTC | 5977 |
| rs781167336 | snp | A/T | 4.36291e-05 | 0.0046704 | missense, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65343803 | AAGACTATGAAGAAG[A/T]TACTCCCAAGCGTCG | 5977 |
| rs781192491 | in-del | -/CTCCTTGCTCTGACTTTGCAGCA | | | intron-variant | DPF2 | GRCh38.p7 | 11:65338430 | AAAACTGTTTCCAGC[-/CTCCTTGCTCTGACTTTGCAGCA]CTCGCCAGCCTGGCC | 5977 |
| rs781314167 | snp | C/T | 1.65488e-05 | 0.00287647 | intron-variant | DPF2 | GRCh38.p7 | 11:65343980 | GGGTGTCTCTTTGCT[C/T]TTCTTGGCAGGGTAA | 5977 |
| rs781324361 | snp | C/T | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333190 | AGTGGCTCACTGGAG[C/T]CTCAAACTCCTGGGC | 5977 |
| rs781511855 | snp | C/G | 1.64914e-05 | 0.00287149 | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65351784 | CCACCTGCTCCCCGA[C/G]ATATCTAAGGCTGTT | 5977 |
| rs781698186 | snp | C/G | 3.38771e-05 | 0.00411551 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65333873 | TCTCGGCCCGAGGCA[C/G]AGGAACAGGGAAGAT | 5977 |
| rs781732459 | snp | C/T | 1.68755e-05 | 0.00290473 | intron-variant | DPF2 | GRCh38.p7 | 11:65346201 | GGAGCTCCTCTCTTC[C/T]CCCCGCATTTCCGAC | 5977 |
| rs796085345 | snp | G/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65337502 | ATATATATATATATA[G/T]ATAGAGAGAGAGAGA | 5977 |
| rs796233573 | in-del | -/AA | | | intron-variant | DPF2 | GRCh38.p7 | 11:65348612 | GCTTGGGCTTTAGGG[-/AA]AAAAAAAAAAAAAAA | 5977 |
| rs796265817 | in-del | CCCGTG/T | | | intron-variant, upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65334328 | CCGTCCCGTCCCGTT[CCCGTG/T]GCTGCAGCAACAGGC | 5977 |
| rs796281682 | in-del | -/CA | | | intron-variant | DPF2 | GRCh38.p7 | 11:65343299 | AGCGAAACTCTGTCT[-/CA]AAAAAAAAAAAAAAA | 5977 |
| rs796318242 | snp | C/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65351271 | CATAGTCAATATTAA[C/T]AAACAAGGAATGACC | 5977 |
| rs796580307 | snp | A/G | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65332901 | CTCAGCTTCTTGTAC[A/G]GCTTTCTTGTGTGTA | 5977 |
| rs796630765 | snp | C/T | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65332508 | GCTGGAGTGCAGTGG[C/T]GCGATCTTGGCTCAC | 5977 |
| rs796698779 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB | DPF2, TIGD3 | GRCh38.p7 | 11:65353083 | TAATGTTTTGAAATA[C/T]AGCTTTTTTCCCCCC | 5977 |
| rs796911157 | snp | C/T | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333296 | TTTCTTTTTCTTTTT[C/T]TCCTTTATTTATTTA | 5977 |
| rs796947018 | in-del | -/TA | | | upstream-variant-2KB | DPF2 | GRCh38.p7 | 11:65333000 | ATATATATATATATA[-/TA]CATATGTATATATAT | 5977 |
| rs796980855 | snp | G/T | | | intron-variant | DPF2 | GRCh38.p7 | 11:65337849 | CGCTCTTGTTGCCCA[G/T]GCTGGAGTGCAATGG | 5977 |
| rs797008298 | in-del | -/CT | | | utr-variant-3-prime, nc-transcript-variant | DPF2 | GRCh38.p7 | 11:65352112 | GAGCAGCTCACTTCT[-/CT]GTGTTCTGCCTCCCC | 5977 |